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Global
Mercury Assessment
CHAPTER 8
Prevention and control technologies and practices
8.1 Overview
600.
This chapter summarizes information submitted from around the world
about prevention and control technologies and practices, and their
associated costs and effectiveness, that could reduce and/or eliminate
releases of mercury, including the use of suitable substitutes, where
applicable.
601.
As noted in chapter 6, the sources of releases of mercury to the
biosphere can be grouped in four major categories (including the last
category, that is not clearly explained in many reviews of the subject
):
-
Natural sources
- releases due to natural mobilisation of naturally occurring mercury from
the Earth's crust, such as volcanic activity and weathering of rocks;
-
Current anthropogenic (associated with human activity) releases
from the mobilisation of mercury impurities in raw materials such
as fossil fuels – particularly coal, and to a lesser extent gas and oil
– and other extracted, treated and recycled minerals;
-
Current anthropogenic releases resulting from mercury used
intentionally in products and processes, due to releases during
manufacturing, leaks, disposal or incineration of spent products or other
releases;
-
Re-mobilisation
of historic anthropogenic mercury releases previously deposited in soils,
sediments, water bodies, landfills and waste/tailings piles.
602.
Figure 8.1 shows graphically these primary release categories,
together with the main alternatives for preventing and controlling
releases.
Figure
8.1
Key sources of mercury releases to the environment, and main
control options.
603.
Releases due to natural mobilisation of mercury and re-mobilisation
of anthropogenic mercury previously deposited in soils, sediments and
water bodies are not well understood and are largely beyond human control.
The other two categories are current anthropogenic mercury
releases. Reducing or
eliminating these releases may require:
-
Investments in controlling releases from
and substituting the use of mercury-contaminated raw materials and
feedstocks, the main source of mercury releases from unintentional uses;
and
-
Reducing or eliminating the use of
mercury in products and processes, the main source of releases caused by
the “intentional” use of mercury.
604.
The specific methods for controlling mercury releases from these
sources vary widely, depending upon local circumstances, but fall
generally under the following four groups:
A.
Reducing mercury mining and
consumption of raw materials and products that generate
mercury releases;
B.
Substitution (or elimination) of
products, processes and practices containing or using
mercury with
non-mercury alternatives;
C.
Controlling mercury releases through
end-of-pipe techniques;
D.
Mercury waste management.
605.
The first two of these are “preventive” measures – preventing
some uses or releases of mercury from occurring at all. The latter two are
“control” measures, which reduce (or delay) some releases from
reaching the environment. Within
these very general groupings are a large number of specific techniques and
strategies for reducing mercury releases and exposures.
Whether or not they are applied in different countries depends upon
government and local priorities, information and education about possible
risks, the legal framework, enforcement, implementation costs, perceived
benefits and other factors.
A.
Reducing consumption of raw materials and products that generate
mercury releases
606.
Reducing consumption of raw materials and products that generate
mercury releases is a preventive measure that is most often targeted at
mercury containing products and processes, but may also result from
improved efficiencies in the use of raw materials or in the use of fuels
for power generation. This
group of measures could potentially include the choice of an alternative
raw material such as using natural gas for power generation instead of
coal, or possibly by using a coal type with special constituents (such as
more chlorine) because the mercury emissions from burning this type of
coal might be easier to control than other coal types.
607.
Another possible approach in some regions might be the use of coal
with a lower trace mercury content (mercury concentrations appear to vary
considerably in some regions depending on the origin of the raw
materials). However, there
are some limitations and potential problems with this approach.
For example, in the case of the utility preference for low-sulfur
crude oil, it is likely that some utilities might be willing to pay more
for low-mercury coal, which effectively lowers the market value of all
high-mercury coal, which in turn might lead to higher consumption of
high-mercury coal in regions where utilities have less rigorous emissions
controls. Moreover, data
collected recently in the US indicate that coal supplies in the US do not
vary significantly in mercury content.
608.
Nonetheless, such preventive measures aimed at reducing mercury
emissions are generally cost-effective, except in cases where an
alternative raw material is significantly more expensive or where other
problems limit this approach.
B.
Substitution of products and processes containing or using mercury
609.
Substitution of products and processes containing or using mercury
with products and processes without mercury may be one of the most
powerful preventive measures for influencing the entire flow of mercury
through the economy and environment.
It may substantially reduce mercury in households (and reduce
accidental releases, as from a broken thermometer), the environment, the
waste stream, incinerator emissions and landfills.
Substitutions are mostly cost-effective, especially as they are
demanded by a larger and larger market.
This group of measures would also include the conversion of a
fossil-fueled generating plant to a non-fossil technology.
610.
At the same time, it would be a mistake to assume that substitution
is always a clear winner. For example, in the case of energy-efficient
fluorescent lamps, as long as there are no competitive substitutes that do
not contain mercury, it is generally preferable from a product-life-cycle
perspective to use a mercury-containing energy-efficient lamp rather than
to use a less efficient standard incandescent lamp containing no mercury,
as a result of current electricity production practises.
C.
Controlling mercury emissions through end-of-pipe techniques
611.
Controlling mercury emissions through end-of-pipe techniques, such
as exhaust gas filtering, may be especially appropriate to raw materials
with trace mercury contamination, including fossil-fueled power plants,
cement production (in which the lime raw material often contains trace
mercury), the extraction and processing of primary raw materials such as
iron and steel, ferromanganese, zinc, gold and other non-ferrous metals
and the processing of secondary raw materials such as iron and steel
scrap. Existing control
technologies that reduce SO2, NOx and PM for
coal-fired boilers and incinerators, while not yet widely used in many
countries, also yield some level of mercury control. For coal-fired
boilers, reductions range from 0 to 96 percent, depending on coal type,
boiler design, and emission control equipment. On average, the lower the
coal rank, the lower the mercury reductions; however, reductions may also
vary within a given coal rank. Technology for additional mercury control
is under development and demonstration, but is not commercially deployed.
In the long run, integrated control strategies that target multiple
pollutants including SO2, NOx, PM and mercury may be
a cost-effective approach. However,
end-of-pipe control technologies, while mitigating the problem of
atmospheric mercury pollution, still result in mercury wastes that are
potential sources of future emissions and must be disposed of or reused in
an environmentally acceptable manner.
D.
Mercury waste management
612.
Mercury wastes, including those residues recovered by end-of-pipe
technologies, constitute a special category of mercury releases, with the
potential to affect populations far from the initial source of the
mercury. Mercury waste
management, the fourth “control” measure mentioned above, may consist
of rendering inert the mercury content of waste, followed by controlled
landfill, or it may not treat the waste prior to landfill. In Sweden, the only acceptable disposal of mercury waste now
consists of “final storage” of the treated waste deep underground, although
some technical aspects of this method are yet to be finalised (see further
discussion below).
613.
Mercury waste management has become more complex as more mercury is
collected from a greater variety of sources, including gas filtering
products, sludges from the chlor-alkali industry, ashes, slags, and inert
mineral residues, as well as used fluorescent tubes, batteries and other
products that are often not recycled.
Low concentrations of mercury in waste are generally permitted in
normal landfills, while some nations only allow waste with higher mercury
concentrations to be deposited in landfills that are designed with
enhanced release control technologies to limit mercury leaching and
evaporation. The cost of
acceptable disposal of mercury waste in some countries is such that many
producers now investigate whether alternatives exist in which they would
not have to produce and deal with mercury waste.
Mercury waste management, as it is most commonly done today, in
accordance with national and local regulations, increasingly requires
long-term oversight and investment. Proper
management of mercury wastes is important to reduce releases to the
environment, such as those that occur due to spills (i.e. from broken
thermometers and manometers) or releases that occur over time due to
leakage from certain uses (e.g., auto switches,
dental amalgams). In
addition, given that there is a market demand for mercury, collection of
mercury-containing products for recycling limits the need for new mercury
mining.
Emission
prevention and control measures
614.
As illustrated in Figure 8.1, a well thought-out combination of
emission prevention and control measures is an effective way to achieve
optimal reduction of mercury releases.
If one considers some of the more important sources of
anthropogenic mercury releases described in previous chapters, one may see
how prevention and control measures might be combined and applied to these
sources:
-
Mercury emissions from municipal and
medical waste incinerators may be reduced by separating the small
fraction of mercury containing waste before it is combusted. For example,
in the USA, free household mercury waste collections have been very
successful in turning up significant quantities of mercury-containing
products and even jars of elemental mercury.
Also, separation programmes have proved successful in the hospital
sector and a number of hospitals have pledged to avoid purchasing
mercury-containing products through joint industry-NGO-Government
programmes. However,
separation programmes are sometimes difficult or costly to implement
widely, especially when dealing with the general public.
In such cases a better long-term solution may be to strongly
encourage the substitution of non-mercury products for those containing
mercury. As a medium term
solution, separation programs may be pursued, and mercury removed from the
combustion stack gases. Mercury emissions from medical and municipal waste
incineration can be controlled relatively well by addition of a carbon
sorbent to existing PM and SO2 control equipment, however,
control is not 100% effective and mercury-containing wastes are generated
from the process;
-
Mercury emissions from utility and
non-utility boilers, especially those burning coal, may be effectively
addressed through pre-combustion coal cleaning, reducing the quantities of
coal consumed through increased energy efficiency, end-of-pipe measures
such as stack gas cleaning and/or switching to non-coal fuel sources, if
possible. Another potential approach might be the use of coal with a lower
mercury content. Coal
cleaning and other pre-treatment options can certainly be used for
reducing mercury emissions when they are viable and cost-effective. Also,
additional mercury capture may be achieved by the introduction of a
sorbent prior to existing SO2 and PM control technologies.
These technologies are under development and demonstration, but are not
yet commercially deployed. Also, by-products of these processes are
potential sources of future emissions and must be disposed of or reused in
an environmentally acceptable manner;
-
Mercury emissions due to trace
contamination of raw materials or feedstocks such as in the cement,
mining and metallurgical industries may be reduced by end-of-pipe
controls, and sometimes by selecting a raw material or feedstock with
lower trace contamination, if possible.
-
Mercury
emissions during scrap steel production,
scrap yards, shredders and secondary steel production, result primarily from convenience light and anti-lock brake system (ABS)
switches in motor vehicles; therefore a solution may include effective
switch removal/collection programmes;
-
Mercury releases and health hazards from artisanal
gold mining activities may be reduced by educating the miners and
their families about hazards, by promoting certain techniques that are
safer and that use less or no mercury and, where feasible, by putting in
place facilities where the miners can take concentrated ores for the final
refining process. Some countries have tried banning the use of mercury by
artisanal miners, which may serve to encourage their use of central
processing facilities, for example, but enforcement of such a ban can be
difficult;
-
Mercury releases and occupational
exposures during chlor-alkali production may be substantially
reduced through strict mercury accounting procedures, “good
housekeeping” measures to keep mercury from being dispersed, properly
filtering exhaust air from the facility and careful handling and proper
disposal of mercury wastes. There
are a number of specific prevention methods to reduce mercury emissions to
the atmosphere. The US chlor-alkali
industry invented the use of ultraviolet lights to reveal mercury vapour
leaks from production equipment, so that they could be plugged. Equipment
is allowed to cool before it is opened, reducing mercury emissions to the
atmosphere. A continuous mercury vapour analyser can be employed to detect
mercury vapour leaks and to alert workers so that they can take remedial
measures. The generally accepted long-term solution is to encourage the
orderly phase-out of chlor-alkali production processes that require
mercury, and their substitution with technologies that are mercury free;
-
Mercury releases and exposures related to
mercury-containing paints, soaps, various
switch applications, thermostats, thermometers, manometers, and barometers,
as well as contact lens solutions, pharmaceuticals and cosmetics
may be reduced by substituting these products with non-mercury products;
-
Mercury releases from dental practices
may be reduced by preparing mercury amalgams more efficiently, by
substituting other materials for mercury amalgams, and by installing
appropriate traps in the wastewater system;
-
Mercury emissions from dental amalgams
during cremation may only be reduced by removing the amalgams
before cremation, which is not a common practice, or by filtering the
gaseous emissions when the practice takes place in a crematorium.
Since a flue gas cleaner is an expensive control technique for a
crematorium, there might be a strong argument for prevention by
substituting other materials for mercury amalgams during normal dental
care;
-
In cases of uncontrolled disposal of
mercury containing products or wastes, possible reductions in releases
from such practises might be obtained by making these practices illegal
and adequately enforcing the law, by enhancing access to hazardous waste
facilities, and, over the longer term, by reducing the quantities of
mercury involved through a range of measures encouraging the substitution
of non-mercury products and processes.
615.
When one considers the broad range of restrictions and controls
increasingly applied to mercury products and processes as summarized in
table 8.1 below and the large (and increasing) resources required to
adequately monitor and enforce these measures, one better understands a
statement by the Japanese Ministry of Environment (JME, 1997), looking
back on the Minamata disaster, and Japan’s difficulty in recovering from
that experience:
“From
the purely economic standpoint, too, a large amount of cost and a great
deal of time are required to deal with such damages, and, when we compare
these costs incurred vs. the cost of the measures that could have
prevented the pollution, allowing such pollution is certainly not an
economically advisable option.”
Table
8.1 Possible restrictions and controls on mercury (adapted from the
submission from the Nordic
Council of Ministers, sub84gov)
|
Mercury
production, use and control restrictions in place in various
countries
|
-
Prevent
or limit the intentional use of mercury in processes
-
Prevent
or limit mercury from industrial processes (such as chlor-alkali
and metallurgic industry) from being released directly to
the environment
-
Apply
emission control technologies to limit emissions of
mercury from combustion of fossil fuels and processing of
mineral materials
-
Prevent
or limit the release of mercury from processes to the
wastewater treatment system
-
Prevent
or limit use of obsolete technology and/or require use of
best available technology to reduce or prevent mercury
releases
-
Prevent
or limit products containing mercury from being marketed
nationally
-
Prevent
products containing mercury from being exported
-
Prevent
or limit the use of already purchased mercury and
mercury-containing products
-
Limit
the allowable content of mercury present as impurities in
high-volume materials (packaging, etc)
-
Limit
the allowable content of mercury in commercial foodstuffs,
particularly fish, and provide guidance (based on same or
other limits values) regarding consumption of contaminated
fish
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|
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Mercury
disposal restrictions in place in various countries
|
-
Prevent
mercury in products and process waste from being released
directly to the environment, by efficient waste collection
-
Prevent
mercury in products and process waste from being mixed
with less hazardous waste in the general waste stream, by
separate collection and treatment
-
Prevent
or limit mercury releases to the environment from
treatment of household waste, hazardous waste and medical
waste by emission control technologies
-
Set
limit values for the allowable mercury content in sewage
sludge spread on agricultural land
-
Restrict
the use of solid incineration residues in road-building,
construction and other applications
-
Prevent
the re-marketing of used, recycled mercury
|
|
|
|
Mercury
control options under consideration
|
-
Prevent
or limit the dedicated mining of virgin mercury from the
Earth's crust
-
Prevent
or limit the marketing of mercury recovered as a
by-product from other mineral or fossil fuel extraction
(such as non-ferrous mining activities and natural gas
cleaning)
-
Control
trade of pure mercury in order to restrict it to
pre-defined essential uses and secure environmentally safe
handling (similar to procedures for hazardous waste)
-
Limit
the allowable content of mercury present as impurities in
fuels and other bulk mineral materials
|
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8.2 Substitution
616.
As described in chapter 6, the deliberate use of mercury in
products and processes comprises a significant contribution to the
mobilisation and release of mercury to the environment.
As the general awareness of mercury's adverse effects on human
health and the environment has increased, a number of countries have made
special efforts to address mercury in these applications, and have had
particular success in reducing mercury use.
Canada, Denmark, Norway, Sweden and the USA, among others, have
seen the number of applications as well as the quantities of mercury used
per application decrease significantly, particularly during the last 15-20
years. Nevertheless, since
many mercury-containing products have long technical lives, it should be
kept in mind that even if a country decides to ban the marketing and use
of mercury in most products, it may take decades before most of the
mercury in use is collected and removed from human circulation.
617.
Today, alternatives are commercially available for virtually all
applications of mercury, permitting a near-total phase-out of mercury use
in countries that pursue such an objective.
However, the Swedish and Danish experiences demonstrate that the
public authorities must have a firm commitment and a clear strategy in
place. During the
implementation of the Swedish ban on mercury in products (except those few
products with an exemption), an investigation of substitutes for
mercury-containing measuring instruments and electrical components was
carried out. It was
discovered that while several applications of mercury were being phased
out, some new applications, surprisingly, were appearing - as in
electronic equipment - even though alternative technologies were
available. It was determined
that users of mercury-containing products are faced with four main
obstacles to the use of viable alternatives.
These include:
-
The need for developing and testing
efforts, e.g. required for security reasons;
-
Higher costs and competition;
-
Attitudes to, and knowledge of,
alternative techniques – even among equipment suppliers;
-
Internationally standardised
measurements.
618.
These are not insurmountable obstacles, but they may require an
appropriate programme of information and incentives.
A summary of common mercury products and substitutes is provided in
table 8.2 below. Because it
is only representative of the great range of mercury applications, this
table does not attempt to include all mercury applications or all
substitutes. Further
information may be found in the references, especially the submission from
the Nordic Council of Ministers (sub84gov).
Table
8.2 Summary of alternatives to principle mercury uses, with some
indications of relative cost
(see notes below table).
|
Product
or
application
|
Alternative(s)
|
General
cost relative to mercury technology
|
|
|
Use of the mercury cell process for producing
chlorine, alkali, sodium hydroxide, potassium hydroxide,
commonly referred to as chlor-alkali
|
Best Available Technology (BAT) for the production
of chlor-alkali is considered to be membrane technology.
Non-asbestos diaphragm technology can also be considered as
BAT.
|
|
|
|
|
|
|
|
Capital investment costs for conversion to the other
processes are significant, but electricity and raw material
costs (together comprising about half of total operating
costs) for the membrane process, as well as waste treatment
and disposal costs, are lower than for the mercury cell
process.
EIPPCB (2000)¨, US EPA (1993), Submission from the
Nordic Council of Ministers, Lindley (1997)
|
|
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Dental amalgam
|
As a result of technological advances in recent
years, various newer alternatives (cold silver, gallium,
ceramic, porcelain, polymers, composites, glass ionomers,
etc.) to mercury amalgam fillings are commercially available.
However, the Danish National Board of Health does not deem the
alternatives fully capable of substituting mercury amalgam in
all cases (e.g. fillings in adult molars), and this is also
the current Swedish position. Even the viable alternatives are
not yet widely known or accepted in many countries, as
practitioners generally find it easier to continue using the
techniques with which they are most familiar.
|
|
|
|
|
|
|
|
Some alternatives are less expensive and some are
more expensive than mercury amalgams, some are as easy to
apply and others are more difficult, but none of the
alternatives require the specialized wastewater treatment
equipment that dental professionals need to meet environmental
regulations in many countries.
KEMI (1998), Submission from the Nordic Council of
Ministers, Gustafsson (2001), US EPA (1997)
|
|
|
Mercuric-oxide and mercury-zinc
(medical) “button cell” batteries
|
Virtually mercury-free zinc-air batteries and other
button-cell alternatives (actually still containing less than
10 mg of mercury) have been available for several years. Many
manufacturers no longer produce mercuric-oxide and
mercury-zinc batteries, but they remain a significant problem
in the municipal waste stream of most countries.
|
|
|
|
|
|
|
|
The cost of alternatives may often be higher than
the mercuric-oxide and mercury-zinc batteries, but
municipalities can avoid expensive collection and disposal
schemes.
|
|
|
Other batteries
|
Virtually all other batteries are now available in
standard and rechargeable mercury- and cadmium-free versions.
Only the older battery manufacturing facilities may continue
to produce batteries using the previous techniques and
materials.
|
|
|
|
|
|
|
|
While comparisons are difficult across a broad range
of batteries (and as battery capacities increase), standard
mercury-free batteries generally cost about the same as the
batteries they replace. Rechargeable batteries, on the other
hand, especially the cadmium-free rechargeables, are
significantly more expensive to purchase, although they become
relatively less expensive if recharged more than 10 or 15
times.
|
|
|
Medical
thermometers
|
There are many alternatives to clinical
mercury-thermometers, including electrical and electronic
thermometers, “disposables” designed for a single use,
glass thermometers containing a Ga/In/Sn “alloy”, etc.
|
|
|
|
|
|
|
|
Used mostly for measuring body temperature,
electronic thermometers have become standard in Denmark and
other countries. While they remain somewhat more expensive
than glass mercury thermometers, their price has come down
substantially in recent years. Other alternatives are also
more expensive, although the recently introduced Ga/In/Sn
thermometer should approach the cost of old mercury
thermometers over time.
|
|
|
Other thermometers
|
Non-medical thermometers are used very widely.
Alternatives to mercury as the measuring medium include other
liquids, gas, electrical and electronic (probably the most
common) sensors. The choice of alternative depends on the
temperature range, the specific application, and the need for
precision. (Mercury thermometers are worthless at temperatures
below -39°C, when mercury turns solid)
For temperature readings in buildings, a bimetal
device is often used, or a Pt-100 or thermocouple is used when
a temperature signal needs to be transferred to a controller
or recorder.
Electronic alternatives have several advantages over
mercury. One thermometer can be adjusted to several different
measuring ranges, thereby substituting for several mercury
thermometers. Further, it is possible to read temperatures
digitally and record them remotely. This could reduce the
chance of human error, as well as reduce operating costs.
For a very small number of precision applications,
mercury thermometers are still preferred for technical
reasons, e.g. for calibration of other thermometer types, for
international standards, etc..
|
|
|
|
|
|
|
|
There is such a great range of mercury alternatives
and applications that it can only be said that prices of
alternatives vary widely, but are not necessarily more
expensive.
It should also be noted that, while the initial cost
of a mercury glass thermometer is lower than an electronic
device, the frequency of broken mercury thermometers is
higher, and one electronic thermometer may replace several
mercury ones. If an annual cost is calculated, the price of an
electronic measuring device is probably no higher than the
mercury device it replaces.
Gustafsson (1997), Submission from
the Nordic Council of Ministers, Rasmussen (1992)
|
|
|
Laboratory use of mercury
|
It is entirely possible to restrict mercury use in
school or university laboratories to a few specific,
controllable uses (mainly references and standard reagents).
|
|
|
|
|
|
|
|
This initiative has already been implemented in
Swedish and Danish legislation. The alternatives are generally
no more expensive, and the need for control of mercury sources
in the laboratory is greatly reduced.
|
|
|
Pesticides and
biocides for
different products and processes.
|
The use of mercury in pesticides and biocides has
been discontinued or banned in many countries. Two main
alternatives have been promoted in their place:
1) Use of processes not requiring chemical
pesticides/biocides, and
2) Easily degradable, narrow-targeted substances with minimal
environmental impact.
|
|
|
|
|
|
|
|
These alternatives are in place in many countries.
The range of products and applications is too diverse to make
definitive statements about cost comparisons, although it is
likely that in the majority of cases costs are roughly
comparable, and environmental benefits are considerable.
|
|
|
Pressure measuring and control equipment
|
Mercury is used as a “heavy liquid” in pressure
gauges, pressure switches and pressure transmitters. All of
these may be substituted without any loss of accuracy or
reliability. Three main technologies are used:
·
flexible membranes,
·
piezoelectric crystals and other sensors that change
some physical property when the pressure changes, and
·
fiber-optic pressure sensors, based on light
transmission.
In pressure gauges like U-tube meters, barometers,
and manometers, mercury is used to continuously indicate
pressure differentials. Here, mercury can be replaced by
another liquid, by gas or by other techniques.
Mercury pressure switches are used to measure pressure or
vacuum differentials. They can be replaced by the same
alternatives as for pressure gauges, but also equipped with a
non-mercury breaker switch.
For remote transmission of measurement readings, a pressure
transmitter is often used. A special mercury transmitter is a
circular tube which may contain up to 8 kg of mercury.
Alternatives use a potentiometer or a differential transformer
to measure pressure changes and transmit an electronic signal.
The most common alternative device is a diaphragm sensor.
|
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|
|
|
|
Alternatives based on gas, other liquids or a
mechanical spring show no significant differences in price,
compared to mercury devices. Alternatives in the form of
electric and electronic instruments are only slightly more
expensive, but have several advantages over mercury.
Gustafsson (2001), Rasmussen
(1992), Submission from the Nordic Council of Ministers.
|
|
|
Electrical and electronic components
|
With very few exceptions, there are no technical
obstacles to replacing electrical components, conventional
relays and other contacts (even when these are contained in
level switches, pressure switches, thermostats, etc.) with
equivalent mercury-free components. A number of examples are
given below.
|
|
|
|
|
|
|
|
There are no significant price differences between
conventional mercury and mercury-free relays and contacts,
except for very specific applications. There are also examples
of mercury components, which are more expensive than the
alternatives.
Gustafsson (1997).
|
|
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|
Mercury component
|
Alternative component
|
Application
|
|
|
|
Tilt-switch – silent switch
|
Various, e.g. manual/mechanical (rolling steel ball,
alternative conducting fluid), micro-switch
|
Circuit control, thermostats, communications
|
|
|
Electronic-switch
|
Solid state-switch, optical switch
|
Circuit control, thermostats, communications
|
|
|
Reed-switch – “mercury-wetted”
|
Solid-state-switch, electro-optical-switch,
semi-conductor
|
Communications, circuit control in sensitive
electronic devices
|
|
|
Proximity sensor/switch – “non-touch-contact”
|
inductive sensor
capacitive sensor
photoelectric sensor
ultrasonic
|
shaft rotation, conveyors
conveyors
conveyors
conveyors
|
|
|
Energy-efficient lamps
|
Currently, there are no mercury-free
energy-efficient alternatives to the energy-efficient lamps on
the market, although there are reports of a high-efficiency
non-mercury lamp based on the field-emission effect, which is
said to be starting production in China (see www.lightlab.se/english/products/index.htm),
and a lamp based on diode technology is in research. One can
only prescribe production/use of energy-efficient lamps with a
minimum mercury-content, and collection and treatment of spent
lamps.
According to European Commission Decision
1999/568/EC (amended 9 September 2002), for a manufacturer to
be allowed to use the European Ecolabel on a single-ended
compact fluorescent lamp, the mercury content must not exceed
4 mg, and the life of the lamp must exceed 10,000 hours.
Other mercury-containing light sources exist, mainly
for special, limited purposes and sold in much lower
quantities, although recently introduced and fashionable auto
headlamps containing mercury are a particular concern, as they
are inconvenient to recover and recycle, and perfectly
acceptable non-mercury alternatives are available.
|
|
|
|
|
|
|
|
Low-mercury lamps are slightly more expensive than
those with a bit more mercury.
Incandescent and some other alternative lamps are
less expensive than energy-efficient lamps, but they have a
much higher energy/operating cost.
Falk (1994), Gustafsson (1997), Submission from the
Nordic Council of Ministers.
|
|
|
Artisanal gold extraction
|
One alternative that seems to offer promise is a
non-mercury electrolytic process (see section 8.5.3) started
in Brazil. However, it has been in existence for some 10 years
and does not seem to have convinced the artisanal community.
An alternative is a cyanidation process, which is reportedly
used by many relatively small-scale miners in Mexico and some
elsewhere, despite the fact that it requires greater
investments and greater process skills, and carries its own
hazards.
Another option is the Minataur process developed in
South Africa by the government’s mineral technology research
body, Mintek. This involves treating the ore with hydrochloric
acid in the presence of sodium hypochlorite and then using
sodium metabisulphate or oxalic acid to precipitate the gold
out as a concentrate that is 99.5% fine gold powder.
UNIDO’s approach in addressing this problem is to
encourage the substitution of low recovery, high mercury
consuming and discharging processes with environmentally safe
and high-yield gold extraction alternatives that sharply
reduce or eliminate the use and discharge of mercury.
Depending upon the technique, cost and delivery method, some
proposals are better received than others, but none as yet
have been widely adopted. A typical technique, developed by
Imperial College Consultants (ICON), London, uses
substantially less mercury and has demonstrated a 40-50 %
better gold recovery efficiency.
|
|
|
|
|
|
|
|
The economics of these alternatives have not been
investigated in detail here, but indications (the first
process used on a wide scale, and the second delivering more
gold and using less mercury) are that they are no more
expensive than the traditional mercury process. If they were,
they would not be adopted by the garimpeiros.
CETEM/IMAAC/CYTED (2001), ICON (2000), UNIDO (1997),
UNIDO (2000), MMSD (2002)
|
|
|
Note:
The coloured bar is an indicator of the overall
user/consumer price level for mercury-free alternatives as
compared to mercury technology.
Price-determining factors vary among the uses
(expenses for purchase, use, maintenance etc.), but do not
include external costs.
|
|
|
|
|
|
|
Green
(left) = lower cost alternative,
Orange (centre) = similar cost
Red (right) = higher cost.
|
8.2.1
Denmark’s experience
619.
A good example of the potential achievements of a coherent
substitution strategy is evident from the experience of Denmark.
In recent years Denmark decided to strongly encourage substitutes
for mercury products, including placing a ban on the sale and use of most
mercury products. As in a number of other countries, a substantial decrease in
mercury consumption for intentional uses has been observed. As can be seen in table 8.3, during the period 1983-1993 the
annual consumption of mercury in intentional uses fell from about 16
metric tons in 1982/83 to 6 metric tons in 1992/93, and decreased further
to 1.5 metric tons in 2000/2001. In
the same period, releases to the environment were reduced from an
estimated 6.9-9.9 metric tons in 1983, to 2.3-3.0 tons in 1993 (of which
0.3-0.8 tons originated from trace amounts of mercury in fuels and
minerals). The deposits in (controlled) landfills have increased during
the same period from 1.7-2.9 metric tons to 2.3-4.5 tons, most likely as a
result of increased hazardous waste collection (reflecting the mercury
content of used products, batteries, etc.) and improved filtering of waste
incinerator emissions.
Table
8.3 Estimated changes in annual consumption of mercury in Denmark
(metric tons/year).
Ref.
Submission from the Nordic Council of Ministers (sub84gov),
based on Maag et
al.
(1996), Hansen (1985) and Heron (2001).
|
Year/use
|
1982/83
|
1992/93
|
2000/2001
|
|
Chlor-alkali
production (discontinued in 1997)
|
3.00
|
2.50
|
0
|
|
Dental
amalgam
|
3.1
|
1.80
|
0.9
|
|
Mercury-oxide
batteries
|
2.40
|
0.36
|
0
|
|
Other
batteries
|
2.30
|
0.28
|
~
0
|
|
Measuring
and control equipment
|
0.53
|
0.50
|
0.3
|
|
Electric
and electronic switches
|
0.34
|
0.30
|
~
0
|
|
Light
sources (lamps)
|
0.14
|
0.17
|
0.17
|
|
Medical
thermometers
|
0.75
|
0.05
|
0
|
|
Other
thermometers
|
1.55
|
0.10
|
0
|
|
Laboratory
chemicals
|
0.50
|
0.09
|
0.09
|
|
Other
intentional uses
|
1.48
|
0.03
|
0.03
|
|
Sub-total,
intentional uses
|
16.09
|
6.18
|
1.5
|
|
Impurities
in consumed fuels, minerals and high-volume materials
(non-intentional mobilisation)
|
1.96
|
1.80
|
1.8
|
|
Total
|
18.05
|
7.98
|
3.3
|
Note: Shading indicates graphically the approx. change in quantities of
mercury consumed over time.
8.2.2
Need for further development of substitutes
620.
For a very few applications, representing a relatively small amount
of mercury consumption, more research and development is needed in order
to be able to completely eliminate mercury use (submission
from the Nordic Council of Ministers, sub84gov).
Fluorescent
lamps
621.
For mercury use in fluorescent lamps, which are known for their low
energy consumption, no commercially mature alternatives are yet available.
Work has been done, however, to reduce the amount of mercury needed
in each lamp. From typical
amounts of 20-40 mg of mercury per lamp, lamps with only 3 mg of mercury
are commercially available today. Unfortunately
these modern low-mercury lamps have difficulty in competing on price with
the higher-mercury lamps, and consumers are generally unaware of the
difference between them.
622.
The use of diodes as lights – recently installed in some traffic
lights - has been proposed as an energy-efficient substitute. The
strength of the light source for this application would appear to be
comparable to what is needed for some housing purposes. However, until
mercury-free alternatives are widely deployed, the mercury in fluorescent
lamps may be managed by collection of used lamps and recycling or proper
waste treatment. This has been attempted in a few countries and
localities, but it has been difficult in most cases to achieve significant
collection rates.
Dental
amalgam
623.
As mentioned in chapter 6, mercury amalgam fillings contribute
significantly to the human (metallic) mercury burden.
While there has been substantial developmental work on a range of
alternatives, there is not yet a consensus that substitutes can adequately
replace mercury amalgams in all dental applications.
In Sweden and Denmark voluntary substitution agreements have been
in place for a number of years and the consumption of mercury for dental
use has decreased significantly. In
Denmark mercury amalgams are permitted (until further notice) only in
molars where the fillings are worn.
Chemical
standard analyses
624.
A number of traditionally important chemical standard analyses
involve the use of mercury compounds.
While mercury-free substitutes are generally available, this issue
is mentioned here because it may take time to change standards previously
agreed upon. For example, a
common analysis using mercury is the COD (chemical oxygen demand -
measuring contents of organic matter) analysis, which is widely used to
control and monitor the quality of wastewater.
Other oxygen demand (e.g., the so-called BOD – biological oxygen
demand) analyses are available and are often used.
However, the problem is that the prescriptions of many mandatory
analyses in regulations and individual wastewater release permits specify
the COD analysis, and need to be changed.
This is possible, but requires attention and time.
The Swedish government is considering a ban on mercury use in
chemicals for analyses and reagents from 1 January 2004.
8.3
Reducing mercury releases
625.
Processing of mineral resources at high temperatures, such as
combustion of fossil fuels, roasting and smelting of ores, kiln operations
in the cement industry, as well as incineration of wastes and production
of certain chemicals, results in the release of a number of volatile trace
elements into the atmosphere.
626.
It is often believed that a combustion unit – typically used for
power generation or waste incineration – with an emission control device
removes most or all of the mercury and other heavy metals emitted during
combustion. However, unlike
other heavy metals, mercury has special properties as described in chapter
6, that make it difficult to capture in many control devices.
While some units with control devices do remove mercury quite
effectively,
there are likely tens of thousands of combustion units around the world
with no flue gas cleaning devices at all, or where such devices are not
effective in removing mercury.
627.
While this section is focused on mercury emissions to the
atmosphere, it should be remembered that mercury is a persistent pollutant
that also cycles through other environmental media (e.g., water and soil).
Further, it should be kept in mind that mercury that is captured in
a pollution control device or diverted from an incinerator may still be
released to the environment unless the slags or residues are properly
managed.
628.
Significant parts of the descriptive text in sections 8.3.1 through
8.3.4 below have been based on Pacyna and Pacyna (2000).
8.3.1
Nature of mercury emissions
629.
In order to fully appreciate the relevance of various emission
control technologies, it is first necessary to review the context of these
mercury emissions (Pacyna and Pacyna, 2000, as modified by US comments to
an earlier draft of this report).
-
Concentrations of mercury in coals and
fuel oils vary substantially depending on the type of fuel and its origin.
The mercury in coal may be associated with the organic or the inorganic
constituents (mineral matter) of coal. When it is associated with mineral
matter such as sulfides it can often be removed by physical coal cleaning
techniques. The removal of
mercury from the organic fraction of coal is much more difficult and
costly.
-
Most of the processes generating
atmospheric emissions of mercury employ high temperature.
During these processes, including combustion of fossil fuels,
incineration of wastes, roasting and smelting operations in non-ferrous
and ferrous metallurgy, and cement production, mercury introduced with
input material volatilizes and is converted to elemental mercury (Hg0)
in the high temperature region of the process. As the flue gas is cooled
to flue gas cleaning temperatures the mercury may remain as Hg0
or part of it may be oxidized to ionic mercury [Hg(II)]. Further, Hg0
and/or Hg(II) may be adsorbed onto particles to form particle-bound
mercury [Hg(p)]. The relative magnitude of Hg0, Hg(II), and
Hg(p) in flue gas is called the speciation of mercury.
-
Mercury oxidization can result from
gas-phase or gas-solid reactions (heterogeneous reactions).
Laboratory experiments and thermal-chemical studies have implicated
atomic chlorine (Cl-) and nitrogen oxide (NO2) as
two potential oxidizing agents. Thermal-chemical
equilibrium studies indicate that the preferred oxidation product is HgCl2
when sufficient chlorine is present in the fuel or waste (i.e., when the
concentration of chlorine is substantially higher than the concentration
of mercury in the flue gas). Fly
ash and other surfaces within the combustion system can catalyze or
mediate mercury oxidization reactions. Major factors that affect mercury
speciation are the fuel (or waste) composition, the combustion conditions,
and the type of flue gas cleaning methods used.
-
Various technologies within the same
industry may generate different amounts of atmospheric emissions of
mercury. It can be
generalized for conventional thermal power plants that the plant design,
particularly the burner configuration, fly ash characteristics, etc., have
an impact on the emissions.
-
The major parameters that determine the
amount and characteristics of mercury emitted to the atmosphere from
high-temperature processes are the amount and speciation of mercury
entering the flue gas cleaning devices, the type of flue gas cleaning
devices used, the concentrations of other constituents (chlorine, NOx),
and the temperature at which the flue gas cleaning devices are operated.
8.3.2 Available options
630.
The options available for reducing mercury releases from various
processes may be organized in two categories: non-control-technology
options, and control-technology options.
631.
The best-known non-control-technology options include such
measures as:
-
Conversion to natural gas, oil, or a
non-fossil power generating technology;
-
Improved energy efficiency (reductions of
CO2-emissions as foreseen in the Kyoto Protocol to the UN
Framework Convention on Climate Change are expected to help reduce mercury
emissions from fossil fuel power generation);
-
Banning mercury in products;
-
Taxes or other disincentives to the use
of mercury in products; and
-
Product labeling.
632.
Banning and taxes are reasonably self-explanatory.
Product labelling has advantages and disadvantages, but has proven
rather effective in some cases, in combination with other measures. For
example, in the case of consumer batteries, consumers paid significant
attention to labels concerning the content of mercury and cadmium.
633.
Control-technology options
for reducing releases may be thought of in the following three categories,
which are further elaborated in the next section:
A.
Pre-treatment measures;
B.
Combustion modifications; and
C.
Flue gas cleaning or end-of-pipe
controls.
634.
It should be noted that the descriptions of techniques and
technologies for emission reductions that follow are general, and not
intended to prescribe methods or equipment that should be used to control
mercury releases from any specific site or plant.
The ultimate appropriateness and effectiveness of any given
technique or technology is site specific, and needs to take into
consideration local circumstances.
1.3.3
Reducing mercury emissions from utility and non-utility boilers and
incinerators
A.
Pre-treatment measures
635.
Pre-treatment
measures typically include coal washing, hand-sorting of waste at an
incinerator or disposal site, the production of refuse-derived fuel at an
incinerator site, or the separation of waste at a material recycling and
handling facility.
B.
Combustion modifications
636.
Combustion modifications
act to change the combustion process. These modifications may be used to
reduce mercury concentrations in the process flue gas, or they may be used
to change the characteristics of the flue gas stream so that mercury is
more easily captured in downstream flue gas cleaning equipment. The
modifications may include using technologies such as fluidized bed
combustor, mass burn/waterwall combustor, low-NOx burner, etc.
637.
As an example, combustion modification-based
low-NOx
technologies should reduce mercury emissions in the exhaust gases due to
lower operating temperatures, although very limited information on this
technology makes it difficult to draw firm conclusions.
While some sources indicate that a reasonable reduction can be
achieved, other preliminary results of staged combustion in atmospheric
fluidized bed combustion (AFBC) units indicated that low-NOx
had little effect on trace element emissions.
638.
Switching to the same type of fuel, but with lower mercury content,
which does not involve pretreatment, may also be considered a combustion
modification.
639.
Other examples of modifications that can potentially be used to
improve capture of mercury are combustion modification techniques that
increase the carbon content and subsequent mercury adsorption capacity of
fly ash. Increased fly ash
carbon content occurs during the use of low-NOx burners or the
use of a NOx control technology called reburning.
This results from fuel-rich regions within the combustion system.
While increased mercury capture has been shown to occur with increased fly
ash carbon, this phenomenon has not been used in commercial practice for
the control of mercury emissions, and it should be considered a potential
control option that might be available in the future.
C.
Flue gas treatment (end-of-pipe) controls
640.
Flue gas treatment, or end-of-pipe,
controls are currently deployed for control
of SO2, NOx, and PM: SO2 controls include
a variety of wet and dry scrubbers; NOx may be controlled by
selective catalytic or selective non-catalytic reduction; and PM may be
controlled by fabric filters (FFs) or electrostatic precipitators (ESPs).
There has been extensive testing of the mercury removable capabilities of
these systems on a wide range of coal-fired utility boilers in the USA.
The average results ranged from 0 to 96 percent dependent on a variety of
factors as described in detail below. Generally speaking:
-
A specific technology, or combination of technologies, produced a
range of mercury reduction for any coal type;
-
The type of coal strongly affected the mercury control achieved,
with average percent removal increasing as coal “rank” increased from
lignite through subbituminous to bituminous. Within any given rank, a
range of removals was achieved. Note also that world coals represent a
wider range of coal rank (e.g. brown coal) and characteristics (e.g.
sulfur, ash) than US coals.
641.
Additional mercury control can be achieved by injection of a
sorbent (carbon- and/or calcium-based) prior to the flue gas treatment
system. These technologies are currently under development and
demonstration in the USA, but are not yet commercially deployed.
642.
Research so far has indicated that the most cost-effective approach
to mercury control may be an integrated multipollutant (SO2, NOx,
PM, and mercury) control technology. A number of these technologies are in
the pilot-scale development stage in the USA, but have generally not yet
been demonstrated at full-scale. Recent
Swedish experience has demonstrated the economic as well as technical
efficiency of such systems in full-scale waste incinerators and utility
burners (Hylander et al., 2002, as cited in comments from Uppsala
University, Sweden).
643.
The potential impact of mercury control technology on by-product
utilization and/or disposal needs to be evaluated. For example, increased
mercury concentration in the gypsum collected in flue-gas scrubbers may
exceed the level permitted in wallboard; or an increased carbon content in
the by-product may limit its use in aggregate used for road surfacing.
Furthermore, any by-product must be in a stable form for disposal if it
cannot be utilized. Either of these potential impacts would affect the
cost-effectiveness of the process.
644.
The major mercury capture mechanisms include the adsorption of
mercury onto solid surfaces and the solvation of mercury in liquid
scrubbers. Mercury can be
adsorbed onto fly ash or entrained sorbent particles for subsequent
capture in particulate matter (PM) control devices. Mercury can also be captured in packed beds containing a
variety of sorbents.
645.
Distribution of mercury within the various streams of wet flue gas
desulfurisation (FGD) systems has been studied in a number of countries.
These studies have shown that mercury capture in wet FGD systems depends
on the rank of coal burned, and the design and operating conditions of the
FGD system. Wet FGD scrubbers were generally preceded by PM control
devices (i.e., ESPs or FFs). The total amount of mercury captured in a
boiler equipped with a scrubber depended on the amount of mercury captured
in the upstream PM control device and the soluble Hg2+ captured
by the scrubber. Flue gas from the exhausts of units burning bituminous
coals exhibited higher levels of Hg2+ than
flue gas from burning of lower rank coals; this mercury was readily
captured in the PM control device and downstream scrubber. Mercury in the
exhausts of units burning low rank coals tended to be Hg0, and
mercury capture in these units tended to be minimal. The scrubber
chemistry must also be controlled to insure that Hg2+ that is
dissolved in the scrubber liquor is not converted back to Hg0
and re-entrained in the flue gas. Scrubber sludges must also be handled in
an environmentally acceptable manner.
646.
Pacyna reported that some wet FGD systems are unable to remove more
than 30 percent of the mercury in the flue gas, but in general the removal
efficiency ranges from 30 to 50 percent (Pacyna and Pacyna, 2000).
Short-term tests in the USA have exhibited emission reductions for units
firing bituminous coals that range from 40 to 95 percent. The best capture
was found for a unit equipped with a FF and a wet limestone (a type of FGD) scrubber.
647.
Soluble forms of mercury can be captured in wet scrubbers.
Soluble forms of mercury include mercuric chloride [Hg(Cl2)]
and other ionic forms of mercury. Hg0
is relatively insoluble in aqueous solutions and it must either be
adsorbed onto a solid, or it must be oxidized to an ionic form that can be
captured by scrubbing. Wet FGD systems used on units burning bituminous
coal (which emit relatively more of the water soluble ionic mercury)
perform much better than do such systems on units burning subbituminous
coal (which emit relatively more non-soluble elemental mercury).
648.
Major factors that affect mercury speciation are the fuel (or
waste) composition, the combustion conditions, and the type of flue gas
cleaning methods used. Coal rank and chlorine content are extremely
important factors in the speciation and capture of mercury with different
types of air pollution control technologies. In the USA, bituminous coals
tend to have relatively high concentrations of chlorine (Cl).
This can result in the oxidization of Hg0 to Hg2+ (primarily
HgCl2). The Hg2+ can be adsorbed onto fly ash carbon and
captured in an ESP or FF. Bituminous
pulverized-coal (PC) fired boilers equipped with an ESP or FF may exhibit
total mercury captures ranging from 20 percent to more than 90 percent.
The higher levels of capture are believed to be associated with a
higher fly ash carbon content. However, carbon in fly ash can negatively impact its use as a
by-product in concrete, as well as negatively impact plant heat rate.
Units that burn bituminous coal, and that are equipped with dry flue gas
desulfurization (FGD) scrubbers or wet FGD scrubbers, also exhibit high
levels of mercury capture. In
contrast, low rank US coals (subbituminous coal and lignite) are alkaline,
have a relatively low chlorine content, and have fly ash with a low carbon
content. Mercury in the
exhausts of plants burning low rank coals tends to be predominately Hg0.
The capture of mercury from the flue gas from these plants tends to
be low, whether the units are equipped with an ESP, FF, dry FGD scrubber,
or wet FGD scrubber.
649.
Conventional mercury measurement methods must be carefully
performed to effectively determine the critical speciation distribution
(i.e., Hg0/Hg2+). In addition, continuous emission
monitors (CEMs), intended to provide a direct determination of either
total Hg0 and/or Hg0 and Hg2+ are
currently under development and evaluation in the field.
(1)
Wet FGD systems
650.
Distribution of mercury within various streams of the wet FGD
system was studied in a number of countries.
The relatively low temperatures found in wet scrubber systems
helped many of the more volatile trace elements to condense from the
vapour phase and thus to be removed from the flue gases.
Due to the special characteristics of mercury, wet FGD facilities
are sometimes unable to remove more than 30 percent of the mercury in
exhaust gases. In general,
however, removal efficiency for mercury ranges from 30 to 50 percent (Pacyna and
Pacyna, 2000).
651.
Removal of trace elements from exhaust gases by wet FGD systems has
been studied in the Netherlands, where only pulverized coal-fired
dry-bottom boilers are used, equipped with a high-efficiency electrostatic
precipitator (ESP) and an FGD design that consists of a wet
lime/limestone-gypsum process with “prescrubber.”
Mostly bituminous coals (lower mercury content) imported mainly
from the USA and Australia are burnt.
In one study the mercury concentration upstream of the FGD system
was 3.4 µg/m3 and downstream was 1.0 µg/m3.
The relative distribution of mercury among bottom ash, collected
pulverised-fuel ash and fly-ash in the flue gases and in the vapour phase
was about 10 percent on fine particles and about 90 percent in vapour
phase. 87 percent of the
mercury content of the coal was released in the flue gases, and up to 70
percent of that was removed by the wet FGD system.
About 60 percent of mercury removal takes place in the prescrubber
and about 40 percent in the main scrubber. These
mercury removal stages are summarized
in figure 8.2 below (Pacyna
and Pacyna, 2000).

|
Pulverized
coal-fired dry-bottom boiler
|
Ţ
87% |
High-efficiency
electrostatic precipitator
|
Ţ
78% |
FGD with wet lime/limestone-gypsum process
|
Ţ
23% |
|
|
ß
|
|
ß
|
|
Pre-
scrubber
|
Main
scrubber
|
|
|
|
ß
|
ß
|
|
Residue
13% |
|
Collected
ash
9% |
|
Residue
33% |
Residue
22% |
|
|
Figure
8.2
Reducing mercury emissions with wet FGD systems
652.
Mercury mass balances are difficult to make. They are dependent on
equipment configurations and operating conditions used at each individual
site. For example, the
partitioning of mercury among bottom ash (residue), collected fly ash,
scrubber residues, and stack emissions may vary substantially depending on
the coal rank, the boiler design, plant operating conditions, and the flue
gas cleaning methods used.
(2)
Dry FGD systems
653.
Retention of vapour phase mercury by spray dryers has been
investigated in Scandinavia and the USA for coal combustors and for
incinerators. In summary, the
overall removal of mercury in various spray dry systems varied from about
35 to 85 percent. The highest
removal efficiencies were achieved in spray dry systems fitted with
downstream fabric filters (Pacyna and Pacyna, 2000).
(3)
Mercury-bearing particle emissions
654.
Coal-fired power plants and municipal incinerators are most
frequently equipped with either electrostatic precipitators (ESPs)
or fabric filters. ESPs are
particularly efficient in removing all types of particles with diameters
larger than 0.01 mm, including those bearing mercury after condensation
within exhaust gases. Particles
containing trace elements are concentrated mostly in two size ranges:
1) at ca. 0.15 mm diameter and 2) between 2 and 8 mm diameter.
Mercury can be found on particles in both size ranges.
ESPs can tolerate operating temperatures as high as 720 K (Pacyna
and Pacyna, 2000).
655.
Fabric filters
are also used in coal-fired power plants. The particle collection efficiency (not the same as the
mercury collection efficiency) is always very high, and even for particles
of 0.01 mm diameter, exceeds 99 percent.
However, the durability of fabric filters is very dependent upon
the working temperature and their resistance to chemical attack by
corrosive elements in exhaust gases.
The temperature of exhaust gases often exceeds the temperature
tolerance for fabric filter material, and therefore limits the application
of fabric filters (Pacyna and Pacyna, 2000). According to comments from
the US, fabric filters capable of temperatures seen in coal-fired boilers
are available in the US.
656.
A number of other control technologies and combinations are
employed in utility boilers. Table 8.4 summarizes most of the commonly used control
technologies for North American utility (electrical generating station)
boilers, and their effectiveness at reducing mercury and other polluting
emissions, while table 8.5 provides some more recent measurements of
mercury emissions in the USA (US EPA, 2002).
Table
8.4 Control technologies used in North American utility boilers
(NEG/ECP, 2000)
|
Technology
|
Mercury
control
effectiveness
|
Control
of other
pollutants
|
Availability
and other notes
|
|
Selective
Non-Catalytic
Reduction
|
Unknown
|
30-60%
NOx
reduction
|
Available
and used on utility boilers.
Minor reduced boiler efficiency.
|
|
Selective
Catalytic
Reduction
|
SCR
+ wet scrubber combination may result in substantial mercury
reduction (see below)
|
70->90%
NOx
reduction
|
Available
and used on larger power plants.
Minor reduced boiler efficiency.
SCR catalyst may improve
oxidation of elemental mercury to divalent mercury, which can
be captured in a wet scrubber used for SO2 control.
The ability of SCR to improve the oxidation of Hg for
capture in scrubbers may be highly coal-specific.
|
|
Low
NOx
burners
|
None
|
>50%
NOx
reduction possible
|
Available
and in use on most coal-fired boilers.
SCR and SNCR retrofits provide additional NOx
control beyond low-NOx burners. It has been
postulated that LNBs will improve mercury capture due to the
increase in amount of unburned carbon (i.e., carbon loss on
ignition [LOI]) in the flue gas stream that may act in a
manner similar to activated carbon injection.
|
|
Coal
Cleaning
|
0-78%
|
Average
48% reduction in SO2 emission potential
|
Already
done on most eastern and mid-western coal to reduce sulfur and
improve boiler performance. Mercury removal varies widely,
typically from 10% to 50% with mean removal rate of 21%.
More advanced coal cleaning methods are under
development.
|
|
Wet
Scrubber
|
Up
to 90% removal of oxidized Hg. No removal of elemental Hg
|
80->90%
SO2 removal
|
Already
in use to reduce SO2. Effectiveness for Hg removal
highly dependent on mix of chemical species present and on
other factors including liquid-to-gas ratio, chlorine content,
and coal type.
|
|
Combined
SCR with Wet
Scrubber
|
>80%
removal of overall Hg may be possible for units firing
bituminous coals; effectiveness for units firing subbituminous
coals is uncertain at this time.
|
>90%
SO2 and >90% NOx removal possible
|
SCR
already in use to reduce NOx.
Helps convert elemental Hg to soluble, oxidized form,
thereby allowing for greater removal by downstream wet
scrubber. Results
are based on limited but encouraging data. The
ability of SCR to improve the oxidation of Hg for capture in
scrubbers may be highly coal-specific.
|
|
Dry
scrubber with ESP or FF
|
6-9%
reported by NEG/ECP; recent EPA studies reported average
removal of approx. 63%)
|
80-90%
SO2 removal
|
In
use on only 1% of US boilers (most units apply wet scrubbers).
Removal efficiency for Hg depends on speciation,
temperature, and chlorine content.
Lime scrubbers show better Hg removal in pilot tests.
|
|
Electrostatic
Precipitator (ESP)
|
0-82%
(cold-side ESP) reported by NEG/ECP; EPA found 36% for
bituminous and 3% for subitumninous (see Table 8-5)
|
>99%
PM removal
|
Already
in use for particulate removal.
Cooler temperature improves ESP performance. US EPA
found Hg removal efficiency of 42-83% on oil-fired boilers.
|
|
Fabric
Filter (baghouse)
|
0-73%
reported by NEG/ECP; EPA found 90% for bituminous and 72% for
subbituminous (see Table 8-5)
|
>99%
PM removal
|
Only
filters providing particulate collection efficiencies >99%
appear to reduce significant amounts of Hg, but data are
limited. Again,
lower temperatures appear to improve performance.
Baghouses are more effective than ESPs in controlling
mercury.
|
|
Enhanced
ESP
|
0-50%
at one test unit
|
>99%
PM removal
|
Enhanced
ESPs being developed to capture finer particles may remove
more Hg. At one
test unit Hg removal improved with lower temperature.
|
|
Wet
ESP
|
Around
30% in 2 pilot scale studies
|
56%
mean PM
removal in pilot
studies
|
Wet
ESP being investigated for “polishing” residual emissions
from other controls. May
improve mercury removal.
Lower temperature improves Hg control.
|
|
Combined
ESP/Baghouse
|
34-87%
in 2 pilot facilities
|
>99%
PM removal
|
Combination
technology to achieve very low PM emissions can improve
removal of Hg & other toxics
when
used in conjunction with powdered activated carbon.
|
|
Carbon
injection
|
Recent
full-scale test results indicate about 80% removal with
bituminous coal+ESP+COHPAC and 55-60% with subbituminous
coal+ESP
|
Not
applicable
|
Cost
and removal effectiveness are directly related to the amount
of carbon used. Used carbon may create a hazardous waste
disposal issue. Carbon injection on utility boilers is
currently under development and demonstration, but is not yet
commercially deployed.
|
|
Fuel
Switching
|
>99%
for natural gas
|
>99%
SO2 and PM control;
50-75% NOx
reduction
|
Fuel
switching reduces multiple pollutants, incl. NOx,
SO2, particulates and CO2.
Accounting for multiple pollutant benefits reduces
control costs for mercury alone.
Cost affected by several factors, including fuel costs,
other pollutant control costs, heat rate, facility age,
capacity factor, new plant capital costs and discount rates.
|
Abbreviations:
SNCR - Selective
non-catalytic reduction
ESP - Electrostatic precipitator
SCR
- Selective
catalytic reduction
PM -
Particulate matter
LNB
- Low-NOx
burner
Table
8.5
Recent measurements of mercury control technologies in the USA (US
EPA, 2002)
Average
Mercury Capture by Existing Post-combustion
Control Configurations Used for PC-fired Boilers
|
Post-combustion
Control
Strategy
|
Post-combustion
Emission
Control Device Configuration
|
Average
Mercury Capture by Control Configuration
|
|
Coal
Burned in Pulverized-coal-fired Boiler Unit
|
|
Bituminous
Coal
|
Subbituminous
Coal
|
Lignite
|
|
PM
Control Only
|
CS-ESP
|
36
%
|
3
%
|
-4
%
|
|
HS-ESP
|
9
%
|
6
%
|
Not
tested
|
|
FF
|
90
%
|
72
%
|
Not
tested
|
|
PS
|
Not
tested
|
9
%
|
Not
tested
|
|
PM
Control and
Spray Dryer
Adsorber
|
SDA+ESP
|
Not
tested
|
35
%
|
Not
tested
|
|
SDA+FF
|
98
%
|
24
%
|
0
%
|
|
SDA+FF+SCR
|
98
%
|
Not
tested
|
Not
tested
|
|
PM
Control and
Wet FGD
System (a)
|
PS+FGD
|
12
%
|
-8
%
|
33
%
|
|
CS-ESP+FGD
|
74
%
|
29
%
|
44
%
|
|
HS-ESP+FGD
|
50
%
|
29
%
|
Not
tested
|
|
FF+FGD
|
98
%
|
Not
tested
|
Not
tested
|
|
(a)
Estimated capture across both control devices
SCR -
Selective catalytic reduction
CS-ESP
- Cold-side electrostatic
precipitator
HS-ESP - Hot-side
electrostatic precipitator
FF
-
Fabric filter PS - Particle scrubber
SDA
-
Spray
dryer adsorber system FGD –
Flue gas desulfurization
|
657.
Some control technologies typically serve to reduce emissions of
more than one pollutant and, in fact, have been driven for the most part
by acid rain emission controls. For
example, wet scrubbers reduce both SO2 and mercury.
The technology for NOx reduction (selective catalytic
reduction, or SCR) has also been found to oxidize elemental mercury that
can be effectively captured in a downstream wet scrubber.
The conversion (fuel switching) of coal-fired boilers to burn
natural gas (in a simple cycle gas-fired boiler or combined cycle gas
turbine) offers great potential to reduce emissions of SO2 and
mercury (almost 100 percent) and NOx (70 to 80 percent).
Baghouses (FFs) and electrostatic precipitators (ESPs) control fine
particles and some mercury, while the combination of the two substantially
reduces mercury emissions. These
are examples where multi-pollution controls may reduce mercury emissions,
while specific mercury controls may not be economically feasible (NEG/ECP,
2000).
658.
The US government, academics and industry are collaborating, with
some Canadian support, on programmes to determine the extent of affordable
mercury reduction from coal fired generating stations.
Conclusions
regarding secondary emissions control
659.
It
must be remembered that the characteristics of the raw material, the
combustion process (or other high temperature process), and the
specifications of the control equipment all influence the eventual
emissions of mercury from the exhaust generated by a given plant. For example, mercury captured with the fly ash from a
bituminous coal-fired boiler equipped with an ESP or FF may range from 36
to 90 percent as seen in table 8.5. Similarly equipped plants burning
sub-bituminous coal or lignite may exhibit fly ash related mercury removal
ranging from 0 to 30 percent of the mercury with the fly ash.
If the plant is also equipped with a wet FGD scrubber (and
depending on the type of coal burned and the scrubber design), nearly all
of the remaining Hg2+ can also be captured. Mercury removal
levels as low as 10 percent and as high as 95 percent have been measured
in the USA for coal-fired utility boilers equipped with wet limestone (FGD) scrubbers (US EPA, 2002). If
coal cleaning is carried out prior to combustion, data from the US
Department of Energy indicate that typically 10 to 50 percent of the mercury in coal can be removed only in the cleaning process (US EPA,
1998). Figure 8.3 provides a simple summary of the most common control technologies, while
table 8.6 briefly reviews other common applications.

|
Sub-
bituminous coals, lignite
|
Commercial coal cleaning
|
Ţ
50-90% |
High-efficiency
electrostatic precipitator
or fabric filter
|
Ţ
35-90% |
Flue gas
desulfurisation
|
Ţ
10-81% |
|
ß
|
|
ß
|
|
ß
|
|
|
Residue
10-50% |
|
Collected
ash
0-27% |
|
Residues
-63% |
|
|
|
|
|
|
|
|
|
|
Bituminous
coals
|
Commercial coal cleaning
|
Ţ
50-90% |
High-efficiency
electrostatic precipitator
or fabric filter
|
Ţ
5-58% |
Flue gas
desulfurisation
|
Ţ
2-52% |
|
ß
|
|
ß
|
|
ß
|
|
|
Residue
10-50% |
|
Collected
ash
18-81% |
|
Residues
1-41% |
|
Figure
8.3
Reducing mercury emissions from utility boilers – typical
efficiencies of key technologies
660.
The
mercury removal efficiencies in figure 8.3 may be compared with impressive
results reported from a coal combustion unit in northeastern China, shown
in figure 8.4.


|
Reciprocating
grate
stoker boiler
or
Traveling grate stoker boiler
|
Ţ
83% |
Dust
separator
|
Ţ
56% |
|
|
ß
|
|
ß
|
|
|
|
Bottom
ash
17% |
|
Fly
ash
17% |
|
|

|
Pulverized
coal
boiler
|
Ţ
93% |
Dust
separator
|
Ţ
70% |
|
|
ß
|
|
ß
|
|
|
|
Bottom
ash
7% |
|
Fly
ash
23% |
|
|
Figure
8.4
Reducing mercury emissions from coal combustion in China (Wang et
al., 2000)
Table
8.6
Efficiency of common mercury control
technologies for utility boilers (based on Pirrone
et
al., 2001)
|
Emission
source and choice of control
technologies for utility boilers
|
Control
combinations, effectiveness, final concentration of mercury
in effluent, etc.
|
|
Coal-fired
utility boiler emission controls
a)
wet flue gas desulfurisation (FGD) system
b)
spray dry FGD system
c)
downstream fabric filter (“baghouse”)
d)
SO2 absorption
e)
high-efficiency electrostatic precipitator (ESP)
f)
FGD wet lime/limestone-gypsum process with pre-scrubber
|
(a) achieves 30-50%
reduction; potentially much better performance on bituminous
coal-fired boilers.
(b) achieves 35-85%
reduction, in the higher range when supplemented by (c)
(e)+(f)
achieve 77% reduction (Netherlands)
(e)+(b)
achieve 75% reduction, of which 50-70% due to (e) (Bergstrom,
1983)
|
|
Coal
fired utility boiler types and characteristics
a)
wet bottom boiler
b)
full burner load
c)
50% burner load
d)
low burner load
e)
fluidized bed combustion
f)
pulverised coal-fired dry bottom boiler
|
(a) produces higher mercury
emissions than alternative boilers
(b) produces similar
mercury emissions as (d)
(c) produces half the
mercury emissions of (b) and (d)
(e) produces similar or lower mercury emissions than
standard boilers
(f)
mercury emissions depend on coal type and control
technologies used
|
|
Oil-fired
utility boilers
a)
tangential unit
b)
horizontal unit
|
(a) and
(b) have comparable mercury emissions
|
|
Abbreviations:
ESP - Electrostatic precipitator
FGD - Flue gas desulfurization
|
D.
Control of incinerator emissions
661.
Various countries rely to a greater or lesser extent on controlled
waste incineration, which reduces the waste volume and (optimally)
makes use of the energy contained in the waste materials.
Because of its low boiling point, most of the mercury content of
the waste evaporates during combustion, and is emitted directly to the
atmosphere, unless the exhaust gas is properly controlled.
In many countries emission controls on waste incinerators have been
improved during the last decade, and this is reflected in decreased
emissions of mercury (AMAP, 2000). In
units fitted with control technologies, Pirrone et
al. (2001) found that 35-85 percent of the mercury is removed by flue
gas controls.
662.
According to compliance tests recently conducted at 115 of the 167
large municipal waste incinerators, MWIs, in the USA, the average and
median mercury control efficiencies for large MWIs were 91.5 percent and
94 percent, respectively. The
average control efficiency at each site was based on a 3-test average
determined by measuring the total flue gas concentration of mercury both
before and after the control system at each site (injection of powdered
activated carbon upstream of either a spray dryer and fabric filter
baghouse, or a spray dryer and electrostatic precipitator).
663.
The mercury eliminated from exhaust gases is retained in
incineration residues and, for some types of filtering technology, in
solid residues from wastewater treatment (from the scrubbing process).
These residues are generally sent to landfills or – depending
upon their content of hazardous materials and other characteristics –
used for special construction purposes (wallboard, roadbeds or similar).
In some cases such solid residues are stored in special deposits
for hazardous waste, which are additionally secured with a membrane or
other cover that eliminates or reduces releases by evaporation and
leaching (Pacyna and Pacyna, 2000).
664.
Typical control efficiencies
for a municipal waste incinerator are shown in figure 8.5 below, and a
greater range of common control measures in table 8.7. Note that
additional releases from deposited ashes and residues are not reflected in
the figure.

|
Municipal
waste
|
Ţ
100% |
High-efficiency
electrostatic precipitator or fabric filter
|
Ţ
40-70% |
Flue
gas
desulfurisation
|
Ţ
15-60% |
|
|
ß
|
|
ß
|
|
ß
|
|
|
|
0%
|
|
collected
ash
30-60% |
|
residues
6-40% |
|
|
Figure
8.5
Reducing mercury emissions from waste incinerators – typical
efficiencies of key
technologies (based on Pirrone et al., 2001)
Table
8.7
Efficiency of common mercury control
technologies for incinerators (based on Pirrone
et al., 2001)
|
Emission
source and control technologies for incinerators
|
Control
combinations, percent reduction of
mercury emissions, final concentration of
mercury in effluent, etc.
|
|
Municipal
waste incinerators (MWI)
a)
mass burn/waterwall (MB/WW) type of combustor
b)
high-efficiency electrostatic precipitator (ESP)
c)
spray dry FGD system
d)
downstream fabric filter (“baghouse”)
|
(a)
emits higher levels of mercury and compounds than
other types of MWI
(b)+(c)
achieve 75% reduction, of which 50-70% by (b) (Bergstrom,
1983)
(c)
achieves typical 35-85% reduction, in the higher
range when supplemented by (d)
|
|
Sewage
sludge incinerators
a)
fluidized bed (FB) combustor
b)
multiple hearth (MH) technique
|
(a)
emits lower levels of mercury to the atmosphere than
other incinerators, and (b) emits more mercury than most
|
|
Abbreviations:
ESP -
Electrostatic precipitator
FB -
Fluidized bed
FGD -
Flue gas desulfurization MH -
Multiple hearth
Note:
This table does not include the use of activated carbon injection
as a control option. However, recent advances in the use of this
technology are mentioned in previous paragraphs.
|
665.
For comparison, figure 8.6 shows the behaviour of mercury in a
specific Japanese incinerator (data provided by the Republic of South
Korea). According to
measurements, 98.2 percent of the mercury in the waste moves to the
emission gas treatment facility, and only 2 percent remains in slag
residues. Then, 14 percent of
the mercury is removed by the electrostatic precipitator and remains in
the collected ash and 91 percent of the mercury that passes the
electrostatic precipitator (77 percent of total mercury) is removed by the
gas cleaning facility. Finally,
7 percent of the mercury originally contained in the waste is emitted to
the atmosphere.

|
Incinerator
|
Ţ
98.2% |
Electrostatic
precipitator
|
Ţ
84.3% |
Gas
cleaning facility FGD
|
Ţ
7.3% |
|
|
ß
|
|
ß
|
|
ß
|
|
|
|
Residue
1.8% |
|
Collected
ash
13.9%
|
|
Gas
cleaning water
77.0%
|
|
|
Figure
8.6
Behaviour of mercury
in a Japanese incinerator (Nakamura, 1994).
8.3.4 Mercury removal from exhaust gases generated in industries other
than utility boilers
and
incinerators
666.
Processing of secondary raw materials such as iron and steel can
also be a significant source of mercury emissions, and emission control
technologies are often necessary. In
this case the origin of the mercury may be from both natural impurities as
well as from the intentional use of mercury in products/components
(switches, air-bag activators etc.) that end up in iron/steel scrap.
667.
Various techniques to remove mercury from exhaust gases generated
by industries other than the production of electricity and heat, as well
as during waste incineration have been developed, particularly for
metallurgical processes. In
one example, a selenium filter has been applied at both steel and
non-ferrous plants. In this
dry media process, mercury removal of 90 percent has been achieved,
reducing the mercury concentrations to below 10 µg/mł.
A carbon filter is also commonly used, with a mercury removal
efficiency similar to that achieved with the selenium filter (Pacyna and
Pacyna, 2000).
668.
The lead sulfide process is another dry media technique used to
remove mercury from flue gases generated in non-ferrous metal smelters.
The gases containing volatile mercury are passed through a tower
packed with lead-sulfide-coated balls.
One study at a Japanese smelter in Naoshima indicates reduction of
mercury concentrations from 1000–5000 µg/mł in the feed to the
absorption tower to 10-50 µg/mł at the outlet (Pacyna and Pacyna, 2000).
669.
The two major wet media processes to remove mercury from flue gases
include the selenium scrubber and the so-called Odda chloride process.
The selenium scrubber method is rather similar to the selenium
filter technique. A mercury
reduction of 90–95 percent can be achieved (Pacyna and Pacyna, 2000).
670.
In the Odda chloride process, mercury vapours are oxidized to form
mercuric chloride, which then precipitates.
Mercury is recovered and mercuric chloride is regenerated.
The mercury concentrations of the treated gases are 50-100 µg/mł
(Pacyna and
Pacyna, 2000).
671.
The effectiveness of these techniques is summarized in table 8.8,
and other common technologies are reviewed in table 8.9.
Table
8.8 Efficiency of flue gas mercury removal techniques
(Pirrone et al., 2001)
|
Control
technique
|
Typical
Hg
removal efficiency
|
Measured
Hg content
downstream (µg/m3)
|
|
Selenium
filter
|
>
90%
|
<
10
|
|
Selenium
scrubber
|
90-95%
|
200
|
|
Carbon
filter
|
90-95%
|
10
|
|
Odda
chloride process
|
n.a.
|
50-100
|
|
Lead
sulfide process
|
90-99%
|
10-50
|
Table
8.9 Efficiency of mercury control technologies for other industries
(based on Pirrone et
al., 2001)
|
Emission
source and
control technologies
|
Control
combinations, percent reduction
of mercury emissions, final concentration
of mercury in effluent, etc.
|
|
Iron
and steel industry
a)
electric arc (EA) process (normally used for special
alloy steels and scrap)
b)
basic oxygen (BO) process
c)
open hearth (OH) process
d)
dry media selenium filter
e)
carbon filter process
f)
wet media selenium scrubber
g)
wet media Odda chloride process
|
(a)
emits 10 times more trace elements than (b) or (c)
(d)
achieves up to 90% reduction of mercury emissions, to
less than 10 µg/mł
(e)
achieves up to 90% reduction of mercury emissions, to
less than 10 µg/mł
(f)
achieves 90-95% reduction of mercury emissions
(g)
may reduce mercury emissions to 50-100 µg/mł
|
|
Non-ferrous
smelting processes
a)
dry medium selenium filter
b)
carbon filter process
c)
dry media lead sulfide process
d)
wet media selenium scrubber
e)
wet media Odda chloride process
|
(a)
achieves up to 90% reduction of mercury emissions, to
less than 10 µg/mł
(b)
achieves up to 90% reduction of mercury emissions, to
less than 10 µg/mł
(c)
may reduce mercury concentrations from 1000-5000
µg/mł
before the absorption tower, to 10-50 µg/mł of emissions at
the outlet
|
8.3.5
Reducing releases of mercury from chlor-alkali facilities
672.
In mercury cell
chlor-alkali plants, mercury is used as a flowing
cathode in electrolytic cells. Specific
details of this process may be found in Lindley (1997), EIPPCB (2000) and
various other references. Most
releases of mercury from this process occur with the hydrogen gas, the
end-box ventilation system and the electrolytic cell room ventilation air
(US EPA, 1973).
673.
Mercury releases from
chlor-alkali operations can be entirely
eliminated only by converting to a non-mercury process such as the
membrane cell process. The
fact that the membrane cell process is more energy efficient (Fauh, 1991)
is one of several strategic and economic considerations that must be taken
into account when a company decides to dismantle a mercury cell chlor-alkali facility and replace it with membrane technology.
674.
When a mercury cell process is converted to a membrane cell
process, certain parts of the process may remain the same.
However, because residual mercury levels exceeding 10 parts per
million (ppm) in the brine system can greatly affect membrane performance
(O'Brien, 1983), a mercury removal system is required initially.
The mercury removal process is needed until residual mercury is
sufficiently purged from the brine (typically 1 or 2 years).
The filters used for mercury removal can later be used for
secondary brine treatment (Horvath, 1986). There are many other technological changes also required when
making a conversion from mercury to membrane technology – although the
complexity and cost of these are highly dependent on the circumstances of
the individual plant. A
typical example is the need for brine of far higher quality for the
membrane process. Supply of
such brine often requires the installation of a new brine purification
plant, and may also require a change of raw material source.
675.
As mentioned, there are electricity savings associated with plant
conversion, as well as other operating cost savings such as the avoidance
of costs of recycling or disposing of mercury wastes, although these costs
are uncertain (US EPA, 1997). While the actual figures are highly plant
dependent, the World Chlorine council has suggested that most estimates
for total operating cost savings fall in the range of $US30 to $50 per
metric ton of chlorine capacity. These
savings, accrued over the plant’s lifetime, may be compared with the
initial investment cost of conversion, which may typically be on the order
of $500 per metric ton of chlorine capacity.
676.
Other than complete conversion to an alternative process, primary
opportunities for reducing atmospheric mercury emissions from the mercury
cell chlor-alkali production process require paying particular attention
to the by-product hydrogen stream, end-box ventilation air, and cell-room
ventilation air. Typical
devices/techniques for removal of mercury from stack emissions are: 1) gas
stream cooling to remove mercury from the hydrogen stream, 2) mist
eliminators, 3) scrubbers, and 4) adsorption on activated charcoal and
molecular sieves. The proper
use of these devices can remove more than 90 percent of the mercury from
the gas streams (Pacyna and Pacyna, 2000).
677.
However, most mercury losses from chlor-alkali facilities are
fugitive. Relevant preventive
measures include:
-
Equipment cool-down before opening for invasive maintenance;
-
Consolidation of maintenance actions to minimize the number of
invasive maintenance events;
-
Draining mercury from a components before it is opened or keeping
its internal mercury covered with cooling water or installing a hood to
capture mercury vapour;
-
Capital investment in larger-capacity decomposers that require less
invasive maintenance;
-
Improving the purity of brine so as to prevent build-up of mercury
wastes that require invasive maintenance;
-
Use of longer-lasting metallic anodes that necessitate less
invasive maintenance;
-
Capital investment in new elongated cells with air pollution
prevention features like internal mechanical arms that can accomplish some
maintenance actions that formerly required invasive maintenance.
678.
Further comprehensive information on relevant abatement options can
be found in EIPPCB (2000) in “Guidelines for Mercury Cell Chlor-alkali
Plants Emission Control: Practices and Techniques,” at
<http://www.cl2.com/AM2001/index.html>, and in a similar series of
guidelines and documents available on the Euro Chlor site at
<http://www.eurochlor.org/>.
679.
As an example of recent progress in this area, the US mercury cell
chlor-alkali companies have voluntarily reduced mercury consumption by 81
percent since 1995 to about 28 metric tons in 2001. Adjusted for a decline
in production capacity during that period, the “real” decrease was 75
percent. According to
industry reports, these reductions have been made through a variety of
equipment upgrades and improvements to housekeeping practices that have
limited the vaporization of mercury from the mercury cell room. Likewise,
using similar technological improvements and changes in management
practices, the industry in Western Europe has voluntarily reduced mercury
emissions to the atmosphere
by 96 percent since 1977.
8.3.6 Reducing mercury releases from artisanal gold mining operations
680.
According to
CETEM/IMAAC/CYTED (2001), since 1980 small-scale gold
mining activities have increased steadily.
This report also estimates that small-scale mining may account for
as much as one-quarter of the world gold output.
Despite the current low gold price, the gold rush in the artisanal
sector continues. Chapter 7
has documented the importance of mercury releases from these activities.
UNIDO’s participation and objective in addressing this problem is
to replace low-recovery, high-mercury-consuming and -discharging processes
with environmentally safe and high-yield gold extraction alternatives that
will sharply reduce or eliminate the use and discharge of mercury.
A.
Diverse measures to reduce mercury releases and exposures
681.
According to
CETEM/IMAAC/CYTED (2001), since training and
awareness-raising are important tools for getting results in the
small-scale mining sector, UNIDO focuses on:
-
On-the job training in cleaner
technology;
-
Training of women and women
entrepreneurs, who have a big share in the sector;
-
Enhancing awareness through workshops on
local, regional and international level;
-
Raising the interest of the media.
Among others, BBC and CNN have already reported on the
mercury-related activities of UNIDO.
682.
In order to successfully introduce alternatives to present
polluting practices, one needs to:
-
Familiarize local manufacturers with the
design of low-tech but efficient gold recovery equipment;
-
Demonstrate alternatives to amalgamation;
-
Prove the cost effectiveness of the new
techniques;
-
Develop micro-financing programmes in
cooperation with the private sector.
683.
The involvement and commitment of the local community is crucial,
including the following elements:
-
Clear community understanding of the
problem;
-
Commitment of community resources to deal
with it;
-
Meetings of all the stakeholders involved
in the discussions to reach a consensus:
-
After consensus is reached, a programme
of action including: a) closed circuit utilization of mercury in the
concentration/amalgamation steps; b) burning of the amalgam in retorts in
the field, and use of fume hoods in gold dealers’ shops; and c)
confinement of processed material in specially built settling ponds;
-
Agreement to adopt these measures both
for the present operations and to avoid future problems;
-
For the present operations, sampling the
levels of mercury pollution, assessing risk areas, and carrying out
isolating and remediating measures to ensure mercury fixation and/or
recovery.
684.
Other more obvious measures should also be implemented, such as:
-
No spilling of mercury during the
amalgamation phase, being a matter of mercury management throughout the
process;
-
Use of amalgamation vessels;
-
Processing of the ore in a closed loop;
-
Use of retorts in order to collect the
mercury vapours;
-
Use of fume hoods (preferably with carbon
filters) at gold shops.
685.
For a field manual on how to process alluvial gold ores and
manipulate mercury safely, see CETEM (1994).
B.
Amalgamation centers
686.
UNIDO (1997) has noted that a very creative solution has been
implemented in Venezuela - Amalgamation Centers.
This solution can be easily reproduced in other countries.
Miners take their gravity concentrates to these centers to be
safely amalgamated by technical operators.
In the Amalgamation Centers in Venezuela operated by the
government, the service is free. In
private centers, miners pay US$ 0.7 per kg of concentrate to be
amalgamated.
687.
Based on the Carhuachi Center, a remarkable Amalgamation Center at
Caroni River, UNIDO and a Venezuelan non-governmental organization known
as PARECA designed a center called UNECA
(UNit for gold Extraction and Controlled Amalgamation).
At the center, gold is processed by trained operators using special
amalgamation plates or leaching using the NaCl electrolytic process.
Both methods reduce the use of mercury.
The electrolytic process actually eliminates amalgamation.
Special retorts and melting furnaces working under fume hoods with
charcoal filters impregnated with iodine are used.
688.
The
UNECA-type amalgamation center is suitable for installation in
mining villages or in any central area to facilitate miners bringing
gravity concentrates. Gold recovery is actually improved and mercury exposure to
the operators is insignificant. For
a miner who takes his concentrate to an amalgamation center, there is the
added benefit of reducing costs in his own processing plant.
These centers play an important role in diffusing information about
mercurialism caused by mercury vapour and ingestion of contaminated fish.
Miners can be given information while they wait for the processing
of their concentrates. The
centers can also provide advice for miners on how to improve their
production, and can provide a meeting place for other purposes of
education and organization.
C.
Individual measures
689.
Other measures may be focused directly at the individual artisanal
miner to reduce his/her releases of mercury.
Retorts can be used to capture volatilized mercury and condense it,
resulting in substantial reductions in air emissions and occupational
exposures, and allowing the mercury to be recycled a couple of times
before its capacity to recover gold has been too much reduced.
Some retorts are made of stainless steel while others are homemade
of inexpensive iron pipes and connections.
Mercury losses during retorting depend on the type of connections
or clamps used, and the mercury recovery is typically 51-99 percent (Farid
et al., 1991). Retorts are not widely used in the goldfields
because of uncertainty among the miners about what may happen to the gold
when they do not have continuous eye contact with the amalgam during the
retorting process. There is some fear that the temperature might be so
high that the gold also evaporates, or that the gold may somehow be
stolen. Moreover, after so many hours of hard work it is thrilling to
watch every step of the transformation of the amalgam to gold. Finally,
those who profit from selling mercury have been reported actively
discouraging any such innovation that may reduce their market.
690.
Other methods for abating mercury emissions when an amalgam is
heated are also available and can be easily implemented.
According to UNIDO (1997), already in 1989 a Brazilian company had
developed a mercury condensing fume-hood.
The prototype had a series of condensing plates coupled with
activated charcoal filters impregnated with an iodine solution.
More than 99.9 percent of mercury from the fumes were reported to
be retained by this special fume-hood.
Less than 40 µg/m3 of mercury was detected in the
interior of the shop during a gold smelting operation, compared with other
measurements as high as 300 µg/m3 in unprotected shops.
A similar technique was used by the Amalgamation Center of
Carhuachi in Venezuela. This
simple solution should be applied to all gold dealers in Latin America,
which will result in a significant reduction of mercury emissions in urban
areas.
8.4 Waste management practices
8.4.1
Mercury wastes and inventories
691.
As described in chapter 6, mercury in waste can be a significant
source of mercury releases, especially as waste management practices vary
considerably around the world. Recalling
from
chapter 6, the diversity of waste streams that need to be carefully
monitored are summarized in
table 8.10. In addition,
there are some very large inventories of mercury that could give rise to
significant releases if not managed responsibly, see table 8.11.
692.
In one example, the US Department of Defense “strategic”
stockpile of virgin mercury was decided to be sold in the early 1990’s.
US EPA subsequently convinced the defence department to delay
further sales until some sort of control system could be worked out to
prevent eventual uses that could not be adequately controlled.
The delay remains in place, but no long-term solution has yet been
found.
693.
In a second example,
chlor-alkali mercury poses a special challenge
(see also section 7.4). As
plants are decommissioned in Western Europe, “used” mercury is
becoming available in large quantities - about 500 metric tons per
year in 2000 and 2001, according to Euro Chlor.
This mercury is virtually “pure” and therefore reusable (for
most applications) without reprocessing. The European Commission was asked
by the Environment Council (meeting 7 June 2001) whether some sort of
coordinated action is necessary within the EU member states in order to
control the eventual fate of this mercury. The industry has agreed for the present to put it under the
control of the Spanish mining company Mińas de Almadén on condition that
it replaces, ton-for-ton, mercury that would otherwise have been newly
mined and smelted to satisfy normal market demand.
Table
8.10
Waste streams giving rise to mercury releases
|
Waste
emissions of mercury to the atmosphere
-
Incinerator
waste water treatment plant sludge
-
Diffuse
releases from uncollected waste products (fluorescent
lamps, batteries, thermometers, mercury switches,
electrical and electronic components, lost teeth with
amalgam fillings etc.)
-
Evaporation of
mercury disposed of in landfills
-
Mercury wastes
that go to municipal, medical or hazardous waste
incinerators
-
Mercury
contained in scrap metal used in secondary metal
production
-
Mercury
emissions from other treatment processes, including
retorting facilities and stabilisation
|
|
Waste
discharges of mercury to water – aquatic environment
-
Direct
discharges from industry and households to water drains
-
Indirect
discharges via waste water treatment systems
-
Informal
disposal in the water, and surface run-off from informal
disposal on land
-
Leachate from
landfills without leachate collecting membranes and
leachate effluent cleaning systems
|
|
Waste
releases of mercury to the soil – terrestrial environment
-
Disposal on
land (informal) or in landfills – with or without
protection of groundwater and surrounding soil
(membranes and leachate water cleaning system)
-
Diffuse
releases from uncollected waste products (batteries,
thermometers, mercury switches, electrical and
electronic components, lost teeth with amalgam fillings
etc.)
-
Local releases
from industry: On site materials and waste storage,
broken/unused pipes, equipment and building materials
-
Spreading of
sewage sludge with trace contaminants on agricultural
land (used as fertiliser)
-
Use of solid
residues from waste incineration and coal combustion for
construction purposes (slag/bottom ash and fly ash)
|
Table
8.11
Key inventories of mercury that must be responsibly managed
|
Waste
quantities or inventories of mercury that need to be managed
-
So-called
“strategic” mercury stockpiles held by a number of
governments
-
Large
quantities of mercury recovered from mercury-cell chor-alkali
facilities at the time of decommissioning or changing to
a non-mercury process
|
8.4.2 Prevention and control measures
694.
Since all of these sources of (potential) mercury releases have
been previously described, this section will focus primarily on the sorts
of measures that may be applied for preventing (long-term solutions) and
controlling (usually short- to medium-term solutions) those releases.
Many problems might be simplified, of course, if mercury
substitutes were more widely used and the mercury content of various waste
streams were much reduced. However,
this chapter assumes that the mercury is already in the waste, and then
suggests how best to deal with it. As
in the case of industrial releases, one may consider a range of
non-technical and technical measures that might be applied.
A.
Non-technical measures
695.
Non-technical measures for preventing and controlling releases from
waste streams may typically be divided among regulatory/prescriptive
measures, economic measures, and educational/information measures.
Some examples follow.
(1)
Regulatory/prescriptive measures
-
Prohibit mercury in product waste and in
process waste from being released directly to the environment, by means of
an effective waste collection service;
-
Prohibit mercury in product waste and in
process waste from being mixed with less hazardous waste in the general
waste stream, by ensuring separate collection and treatment;
-
Set limit values for the allowable
mercury content in sewage sludge spread on agricultural land;
-
Restrict the use of solid incineration
residues in road-building or other applications where its long-term
control cannot be assured;
-
Prohibit the re-marketing of used,
recycled mercury;
-
Prohibit illegal dumping of wastes;
-
Prohibit any direct or indirect
discharges of mercury to normal drains or the water treatment system, or
any disposal of mercury in water;
-
Prohibit or restrict cross-border
transport of mercury (and other hazardous) wastes;
-
Require that any mercury containing waste
or materials stored on-site by an industry or commercial operation must be
in air-tight and waterproof containers, and that the organization must
have a written plan and schedule for eventual proper disposal of the
materials;
-
Prohibit the disposal on land of any
sewage sludge, fertilizer, or other material that exceeds responsible
international standards for mercury content;
-
Put in place an environmental management
strategy that includes responsible monitoring and enforcement of mercury
regulations, tracking of all mercury movements (from raw material to
process to product to waste), and periodic independent control.
(2) Economic measures
-
Set taxes
and fees on hazardous waste disposal (special incineration,
dedicated landfill, etc.) that fully reflect the real
long-term costs to society and the environment of responsibly
dealing with these hazardous substances.
(3) Information and educational measures
-
Educate the public about proper disposal
of mercury containing products;
-
Provide collection points where the
public may easily take these separated products;
-
Devise several key indicators and
publicize the progress that is being made with regard to responsible
management of mercury.
B.
Technical measures
696.
Technical measures for dealing with mercury wastes may be divided
between pre-treatment measures and emission control measures.
(1) Pre-treatment measures
(2) Emission control measures
-
Require landfills to be properly licensed
and equipped for the type of hazardous waste they accept, including
membranes to prevent mercury from evaporating or leaching, collection and
treatment of landfill effluent, routine and long-term testing of
groundwater quality, air emissions, etc.;
-
Ensure that mercury wastes are
incinerated only at facilities equipped for hazardous waste, with
best-available-technology dust collectors and flue gas control, etc.;
-
Develop a facility (perhaps jointly with
a neighboring country) for final disposal of mercury (and other) treated
wastes that are so concentrated or hazardous over the long term that they
cannot be responsibly disposed of in another manner.
C.
Limited long-term solutions
697.
As explained in chapter 6, most of the options above are short- to
medium-term measures. One of the only real long-term measures is prevention
(keeping mercury out of the waste stream).
Once present in the waste stream (if pollution control is
considered a priority), mercury contributes to the need for emission
controls on incinerators, special disposal of incinerator residues,
landfill leachate treatment etc. – all associated with extra costs.
Even those countries that make an effort to separate mercury
products from the general waste stream have found it difficult to achieve
satisfactory collection rates, and they have discovered that separate
collection and treatment implies significant extra costs for society.
Therefore, with regard to mercury in products, minimising the
intentional use of mercury may be a highly desirable objective.
This has been the main driving force behind the mercury
substitution policy of many countries.
698.
Another long-term measure for mercury waste management is
intermediate storage/definitive storage in a special facility, such as
that described below.
8.4.3 Responsible management of mercury inventories
A.
Take-up by Almadén
699.
As described in chapter 7, one of the solutions proposed for
mercury from decommissioned chlor-alkali facilities is shipping it to the
Almadén mercury mine in Spain, which has agreed to decrease its mining
production and to market the chlor-alkali mercury instead.
Some feel that there are not yet adequate controls on where this
mercury would then be sold by Almadén, or how it would be used.
B.
Intermediate storage
700.
Another proposal is that the mercury could be stored safely for an
indefinite period of time until a strategy for closed-loop re-use or safe
disposal is available. This option has the advantage that the mercury would be
available if some important new need is identified.
It could lead to some releases, ongoing management costs, and is
still not a final solution. However, ongoing
management costs and the risk of significant releases outside the
intermediate storage enclosure would be small if best management practices
were implemented.
C.
Terminal/permanent storage
701.
It has been argued that, from an environmental point of view,
terminal/permanent disposal of mercury would be preferable.
However, this could encourage continued mining and smelting of
virgin mercury to meet ongoing demand.
Further, it has been argued, the deposited mercury could be
difficult if not impossible to recover if important new (and
“closed-loop”) uses were to emerge in the future.
702.
Sweden has developed a strategy for terminal storage of surplus
mercury and mercury containing waste. The strategy was developed as a
response to concerns about what to do with the mercury collected from
consumer products, industry and high-level mercury waste, which is
currently in intermediate/provisional storage. Although the legal
framework needs to be developed, and there are various technical issues
related to waste treatment that need to be worked out, as well as the
location and design of the terminal storage facility, a viable concept has
been developed and proposed. The concept includes a suggestion that the
waste owners bear full responsibility for constructing, managing and
operating the facility. Excluding pre-treatment,
estimates of the eventual cost of this option are on the order of $US
14-20 per kg of mercury. To
put this figure in some perspective, this terminal storage cost would add
6-10 percent to the estimated cost of converting a chlor-alkali facility
from the mercury process to the membrane process.
703.
The terminal storage concept is based on the conversion of mercury,
currently stored in the elemental form or as high-level mercury containing
waste, to a chemically stable form (e.g. mercuric sulphide, HgS), and
subsequent disposal of the stabilised mercury in deep-rock storage. A
number of investigations of waste treatment technology, chemical
stabilisation, geochemistry, geohydrology and economics have been carried
out, and the results of these investigations indicate that the concept is
technically and economically feasible.
Although a range of issues remain to be addressed, the terminal storage
strategy is scheduled for implementation in the near future in Sweden.
704.
While other options for waste treatment and facility design will
also be considered, at present the main components of the proposed
terminal storage concept are:
-
Conversion of mercury from high-level
waste, batteries, electrical devices, etc., to the elemental form via
thermal treatment and condensation of liquid elemental mercury;
-
Conversion of the elemental mercury to
the sulphide form via thermal treatment with, e.g., sodium sulphide or
other suitable reagents;
-
Storage of the mercury sulphide in a
deep-rock storage facility equipped with appropriate monitoring devices.
705.
Physical requirements for the terminal storage facility include
geological stability, low water permeability, and absence of mineral
resources which are or may become economically feasible to excavate. The
terminal storage may be located in an abandoned mine shaft with well known
geological and geohydrological characteristics.
706.
It is important to note that the concept of deep-rock terminal
storage was not developed as a method to reduce current mercury releases
to the environment or current exposures. Rather, it was designed as a
long-term solution to the problem of storing mercury wastes - in
light of the persistence of mercury and the need for long-term strategies
to reduce mercury pollution.
8.5 Mercury control costs and effectiveness
707.
While the costs of control technologies are highly variable,
depending on the country and location, local circumstances, availability
of equipment and technicians, characteristics of raw material being
combusted or waste being incinerated etc., this section draws on several
key sources to provide some comparative estimates of these costs.
8.5.1 Costs of reducing mercury emissions from boilers and incinerators
A.
Mercury control costs for utility boilers
708.
As mentioned on page 14 of NEG/ECP (2000), “[US EPA] estimates of
the cost effectiveness of various mercury emission reduction approaches
vary widely,” from $US 11-66 per gram of mercury removed using carbon
injection,
to $US 143-933 per gram of mercury removed for fuel switching.
These figures may appear high compared to general costs for
reducing conventional pollutants such as nitrogen oxides (NOx),
sulfur dioxide (SO2) and particulate matter (PM).
While any such comparison must be carefully interpreted due to the
entirely different nature of the emissions, quantities, effects, etc., US
EPA has presented a comparison as summarized in the box below.
|
Comparison
of Mercury and NOx
Control Costs (US EPA, 2002)
|
|
An
understanding of mercury control costs may be gained by
comparing them with costs of currently used controls for NOx.
In the USA, commercial NOx
control
technologies are being used to comply with emission reduction
requirements. Therefore, the costs associated with these NOx
controls are
being experienced at full-scale applications. A comparison of
mercury control costs with costs of currently used NOx
controls
provides insight into how far or near the mercury control
costs are from costs that are presently being experienced at
full-scale applications to control another pollutant.
Table
8-10 below presents the ranges of total annual costs in 2000
constant dollars for the mercury controls examined in this
work and for two currently used NOx
control
technologies; i.e., low NOx
burner (LNB) and
selective catalytic reduction (SCR). The NOx
control costs
presented are for applications on dry-bottom, wall-fired
pulverized-coal boilers ranging in size from 100 to 1000 MW
and being operated at a capacity factor of 0.65. In general,
costs associated with LNB and SCR are expected to span the
costs of currently used NOx
controls; therefore, these costs were chosen for comparison
with mercury control costs.
As
seen from Table 8-10 below, total annual costs for mercury
controls lie mostly between applicable costs for LNB and SCR.
However, Table 8-9 (not shown here) shows total annual
costs of mercury controls to be higher for the minority of
plants using HS-ESPs (hot-side electrostatic precipitators).
Excluding these costs, both currently estimated and projected
mercury control costs are in the spectrum of LNB and SCR
costs.
Table
8-10
|
Air
pollutant
controlled
|
Control
technology
|
Total
annual
control cost range
($US/MWh generated)
|
|
Hg
|
Powdered
activated carbon injection
|
0.305
to 3.783
(a)
0.183
to 2.270
(b)
|
|
NOx
|
Low-
NOx
burners
|
0.210
to 0.827
(c)
|
|
Selective
catalytic reduction
|
1.846
to 3.619
(c)
|
(a)
current estimate of costs
(b)
projected costs
(c)
actual costs
|
709.
It is important to recognize that the ultimate cost of controlling
mercury from utility boilers will be dependent upon the potential impact
that mercury control has on the sale and/or disposal of the combustion
by-products. For example, for
plants that sell their fly ash for cement manufacturing, the use of
activated carbon injection could dramatically reduce their ability to sell
this material due to increased carbon concentrations. For plants that elect to use a wet scrubber to capture
mercury, their ability to sell their gypsum for use in wallboard
manufacturing could be compromised by increased concentrations of mercury.
The potential impacts of additional mercury control on the use of
by-products or the disposal of residues have not yet been determined. Such
considerations may significantly affect an operator’s costs of
controlling mercury emissions from coal-fired boilers.
710.
It must also be mentioned that mercury presents a far greater
health and environmental hazard on an equivalent weight basis than do SO2,
NOx,
and PM. The costs are more similar to those associated with the
control of dioxins and furans, which are produced in flue gases in
extremely small quantities, and where any emissions at all are a concern.
As is the case with effective controls of these compounds
(scrubbers and baghouses are very effective at capturing dioxins and
furans), it is important to note that many mercury control strategies also
reduce other pollutant emissions, and vice versa.
Fuel switching, for example, can dramatically reduce emissions of
NOx, SO2, carbon dioxide (CO2), and
particulates, while scrubbers remove many other toxics in addition to
mercury. When the costs of
these strategies are allocated among all the pollutants reduced, their
cost-effectiveness is much improved.
711.
Summary information on relative control technology costs is
provided in table 8.12. This table indicates an apparent cost-effectiveness advantage
for activated carbon injection, with the caveat that additional equipment
is needed to remove other pollutants.
However, it also demonstrates the popularity of the combination of
electrostatic precipitator (ESP) or fabric filter (FF) and wet flue gas
desulfurization (FGD), for which the initial investment (for a plant
approaching 1000 MW capacity) is about $US 25 million greater, but
operation & maintenance costs are nearly $US 6 million/yr less than
for activated carbon injection.
Table
8.12
Rough cost-effectiveness of mercury control measures for utility
boilers (based on Pirrone
et
al., 2001). Please refer to the source for
further details.
|
Control options for utility boilers
|
Mercury
removal
efficiency
(percent)
|
Costs
|
|
Investment
($US
1000/MW)
|
Operation
&
maintenance
($US
1000/MW/year)
|
|
ESP only
|
10**
|
1.6
|
0.2
|
|
FF only
|
29**
|
28.9
|
5.8
|
|
ESP or
FF + wet FGD
|
85
|
59.0
|
2.5
|
|
SDA +
ESP
|
67
|
143.
|
5.0
|
|
ESP +
carbon filter bed *
[Based
on the costs noted, this is not a practical option]
|
90-95
|
264.0
|
62.0
|
|
Activated
carbon injection + FF *
|
50-90+
|
34.6
|
8.1
|
|
*
Mercury control technologies.
**
On the basis of previous discussions, this number appears low.
Abbreviations:
ESP -
Electrostatic precipitator
SDA - Spray dryer absorber
FF -
Fabric filter MW - Megawatt
FGD -
Flue gas desulfurization MWh - Megawatt-hour
|
B.
Mercury control costs for incinerators
712.
Incinerators employ many of the same mercury control technologies
used in utility boilers. However, the cost structure is much different, so it is
useful to present them in a separate table, and to compare incinerator
control costs with other incinerator control costs rather than with
utility boiler control costs. Once
again, it should be kept in mind that the costs calculated in table 8.13
assume that the entire cost of emission controls is allocated to mercury
alone, which is clearly not representative of the real world situation.
Each of the control options discussed in the table has some effect
on greenhouse gases and other emissions, and these effects must be taken
into consideration before final decisions on multi-pollutant control
technologies are made.
713.
In conclusion, the relative costs and mercury removal effectiveness
of the most common control technologies applied to incinerators are
presented in table 8.14. In
this case activated carbon injection seems to clearly lead the field in
cost effectiveness, although its ability to remove other pollutants from
the flue gas is greatly limited. It
is therefore combined with an electrostatic precipitator or a fabric
filter.
Table
8.13
Control technologies and cost effectiveness for incinerators (US
EPA, 1997)
|
Source
|
Mercury
control
technique
|
Cost
effectiveness
|
Cost
comments
|
|
$US/g
Hg removed
|
Other
indicators
|
|
Municipal
waste combustor (MWC)
|
Material
separation
(batteries)
|
$3.19
|
$0.41/metric
tons MSW
|
Costs
very community specific; results shown based on one
community's program.
|
|
Product
substitution
(e. g., batteries, thermometers etc.)
|
[see
comment]
|
[see
comment]
|
The
potential for product substitutions requires that the specific
circumstances of each situation be examined; general cost
estimates are not possible.
|
|
Activated
carbon injection
|
$0.46
– 1.92
|
$0.77-3.85
metric tons MSW
|
Costs
assume an 85% reduction; the range of costs covers two model
plants.
Costs equivalent to 1.3% (large unit) to 6.9% (small unit)
calculated cost increase*
|
|
Carbon
filter beds
|
$1.13
– 2.39
|
$5.98-10.33/metric
tons MSW
|
Range
of costs covers two model plants.
|
|
Polishing
wet scrubber
|
$3.52
– 7.31
|
$5.83-14.85/metric
tons MSW
|
Costs
assume an 85 percent reduction; range of costs covers two
model plants.
|
|
Medical
waste incinerator (MWI)
|
Material
separation
(batteries)
|
less
than $3.19
[see comment]
|
less
than $0.41/metric tons MSW [see comment]
|
Costs
vary on a site-specific basis; no costs were available; cost
effectiveness for a hospital program would be assumed to be
better than for a community program.
|
|
Good
combustion, wet scrubber or dry scrubber with carbon
injection
|
--
|
--
|
For
cost- effectiveness estimates for individual facilities, the
reader should consult Hospital/ Medical/ Infectious Waste
Incinerators: Background Information for Promulgated Standards
and Guidelines - Regulatory Impact Analysis for New and
Existing Facilities (EPA- 453/ R- 97- 009b)
|
|
Switching
with waste segregation
|
|
0.01-0.04%
calculated cost increase*
|
|
Switching
without waste segregation
|
|
0.02-0.09%
calculated cost increase*
|
*
“Calculated cost increase” is the estimated cost increase in
the service or product to cover the cost of these emission
controls.
Abbreviation:
MSW - municipal solid waste
Table
8.14 Cost-effectiveness of mercury control measures in waste
incinerators (based on Pirrone
et al., 2001) (ton = metric ton)
|
Control
option
|
Mercury
Removal
efficiency
|
Costs
|
|
Investment
|
Operation
&
maintenance
|
|
Municipal
waste combustor
|
(percent)
|
($US
1000/ton waste)
|
($US
1000/ton waste/yr)
|
|
capacity
of MWC
|
|
~180
t/day
|
~2000
t/day
|
~180
t/day
|
~2000
t/day
|
|
ESP only
|
10
|
n.a.
|
n.a.
|
n.a.
|
n.a.
|
|
FF only
|
29
|
n.a.
|
n.a.
|
n.a.
|
n.a.
|
|
ESP or FF +
carbon filter bed
|
99
|
31.7
|
80.0
|
6.5
|
15.6
|
|
Activated
carbon injection + ESP or FF
|
50-90+
|
0.3
|
0.8
|
0.25
|
1.3
|
|
Polishing
wet scrubber + ESP or FF
|
85
|
10.3
|
22.9
|
1.9
|
4.9
|
|
|
|
Medical
waste incinerator
|
(percent)
|
($US
1000/ton waste)
|
($US
1000/ton waste/yr)
|
|
capacity
of MWI
|
|
~60
kg/hr
|
~460
kg/hr
|
~60
kg/hr
|
~460
kg/hr
|
|
ESP only
|
10
|
n.a.
|
n.a.
|
n.a.
|
n.a.
|
|
FF only
|
29
|
n.a.
|
n.a.
|
n.a.
|
n.a.
|
|
Activated
carbon injection + FF
|
50-90+
|
56.5
|
127.0
|
89.0
|
84.0
|
|
Polishing
wet scrubber + FF
|
85
|
400.0
|
400.0
|
100.0
|
100.0
|
|
Abbreviations:
ESP -
Electrostatic precipitator
MWh - Megawatt-hours
FF -
Fabric filter (baghouse) MWC - Municipal
waste combustor
FGD -
Flue gas desulfurization MWI -
Medical waste incinerator
SDA -
Spray dryer absorber
|
8.5.2 Costs of
chlor-alkali conversion
714.
Pirrone et
al. (2001) and others (Lindley 1997, Fauh
1991, etc.) have noted that the membrane chlor-alkali process is more
energy efficient than the mercury cell process.
They have also pointed out that conversion from the mercury cell to
the membrane process is possible utilizing some of the existing equipment.
While keeping in mind the previous remark that the decision to
convert from mercury cells to another process is not a purely economic
decision, one may look more closely at the costs involved.
715.
Euro Chlor, the association representing the European chlor-alkali
industry, has estimated that conversion of a typical plant from mercury
electrolysis to membrane electrolysis would cost about $US 500 per metric
ton of chlorine capacity. US EPA (1997) produced estimates for conversion
that are roughly in line with those of Euro Chlor. Lindley (1997) also
estimated conversion costs for a typical West European chlor-alkali plant
at the euro equivalent of about $US 500 per metric ton of chlorine
capacity. Harris (2001) has estimated conversion
costs in the range of $US 400-700 per metric ton of chlorine capacity, and
operating cost savings in the range of $30-50 per metric ton of chlorine
capacity, noting that the economic attractiveness of any given project
will be highly dependent on its special circumstances, but concluding that
conversion will be economically attractive only in exceptional cases.
716.
It is informative to compare these high conversion costs with the
striking reductions in mercury emissions (96 percent since 1977) in
European, and in mercury consumption (75 percent since 1995) in the US
chlor-alkali industries in recent years (see chapter 7) through
a variety of equipment upgrades and improvements in housekeeping practices
–
at costs at least 100 times lower per gram of mercury prevented from
entering the environment. In this perspective, the highest near-term
priority, and the greatest reduction in mercury releases for a very modest
investment, might be to extend this experience and these techniques as
rapidly as possible to all other mercury-cell chlor-alkali plants around
the world. Despite the reductions achieved by
such measures, significant consumption of mercury must still be
anticipated until conversion to mercury free technology takes place. The
(US) Chlorine Institute’s and (European) Euro Chlor’s detailed
guidelines on preventing air emissions and other releases should serve to
indicate the most rapid and least expensive way forward.
8.5.3 Costs of dealing with releases from artisanal gold mining
717.
Previously a long list of measures was presented for reducing
releases and exposures from artisanal gold mining practices.
Depending on the measures one wishes to pursue, the range of
related costs is vast. Therefore
the establishment of a typical amalgamation center was selected as an
example of “extreme” measures that may have to be taken in order to
really have a profound effect on a large number of miners in a given
region.
718.
According to UNIDO (1997) the cost of establishing a UNECA-type
center (see section 8.3.6) depends on the process to be adopted
(amalgamation with special plates and/or NaCl electrolytic leaching
process), infrastructure needs, power supply, civil works, material costs,
transportation and labor costs of the mining region. The estimated typical investment and operating costs are
summarized in table 8.15.
|
Non-mercury
processes for recovering gold
|
|
An
electrolytic process to leach gold has also been
developed by CETEM (UNIDO, 1997) - Center of Mineral
Technology, Rio de Janeiro and tested in a pilot plant in
the Tapajós region, Brazil. This process has the potential
to replace amalgamation of gravity concentrates. Material
with 1 ppm Au was mixed with sodium chloride (1 Mol/l),
which is transformed by electrolysis into a mixture of
sodium hypochorite-chlorate. More than 95 percent of the
gold dissolves within 4 hours and is collected on a graphite
cathode. The solution is always recycled minimizing effluent
discharge. The NaCl and energy consumptions are 100
kg/metric ton of ore and 170 kwh/kg of Au respectively.
Plastic leaching tanks are used, reducing investment cost.
So the process is relatively uncomplicated and inexpensive
with the potential for use. The main drawback of course, is
the need for trained personnel to control operating
variables (pH, current density, etc).
The
UNECA-type Processing Center is suitable for installation in
mining villages or in any central area to facilitate
transportation of gravity concentrates. Gold recovery is
actually improved and mercury exposure to the operators is
insignificant. For a miner who takes his concentrate to a
Processing Center, there is the additional benefit of
reducing costs in his own processing plant. These Centers
play an important role in bringing information about
mercurialism caused by mercury vapour and contaminated fish
ingestion. Miners can be given brochures and additional
instructions while they wait for the processing of their
concentrates. The Centers can provide advice for miners on
how to improve their production and can provide a meeting
place for other purposes of education and organization.
Another
option has been reported from South Africa (MMSD, 2002),
where the government’s mineral technology research body,
Mintek, has developed the new Minataur process. This
involves treating the ore with hydrochloric acid in the
presence of sodium hypochlorite and then using sodium
metabisulphate or oxalic acid to precipitate the gold out as
a concentrate that is 99.5% fine gold powder.
|
Table
8.15
Estimated capital cost of a UNECA Center (based on UNIDO, 1997)
|
Estimated
fixed capital costs (equipment)
|
US$
|
|
Amalgamation-plates
(2 sluices of eight 30x40 cm plates each in metallic frame)
|
20,000
|
|
Fume
hoods, air filters, scrubbers, retorts, melting furnace
|
39,000
|
|
Electrolytic
leaching system incl. filters and activated charcoal column
|
60,000
|
|
Other
|
10,000
|
|
Subtotal
fixed capital costs
|
129,000
|
|
Estimated
variable capital costs
|
|
|
Civil
construction + water works
|
20,000
|
|
Mechanical
+ electrical
|
10,000
|
|
Personnel
costs (Engineer, laborers, expenses, training)
|
88,000
|
|
Subtotal
variable capital costs
|
118,000
|
|
TOTAL
CAPITAL COSTS
|
247,000
|
719.
The costs presented in table 8.15 do not include power supply,
which must be available on site, or the cost of land, which could be
arranged by the local community. The total capital investment of nearly US$ 250,000 is high,
but it can be greatly reduced after the installation of the first center
as many local personnel can be trained, and as technology is transferred
to local technical people who can be in charge of building other centers.
720.
In addition to capital cost, one must consider operating cost, as
presented in table 8.16.
Table
8.16 Estimated monthly operating costs for a UNECA Center (based on
UNIDO, 1997)
|
Estimated
operating costs
|
US$/month
|
|
·
Labor
& security personnel
|
4,900
|
|
·
Electricity
& gas
|
1,500
|
|
·
Supplies
& maintenance
|
6,000
|
|
·
Mercury
monitoring
|
500
|
|
·
Proper disposal, etc.
|
2,000
|
|
TOTAL
|
14,900
|
721.
As in Venezuela, the UNECA Center can charge US$ 1/kg of
concentrate processed, thereby deriving an income of about US$
10,000/month. This nearly
covers the operating cost. The
UNECA Centers are also decontamination centers.
Using the electrolytic process, residual mercury and gold can be
extracted from dredged “hot spots”.
Likewise, tailings produced by individual miners who continue to
amalgamate their concentrates can also be treated in the Center.
As the gold content in amalgamation tailings is high, as observed
in Venezuela, the decontamination step might be profitably conducted by
private companies. The Center
should provide a safe landfill for the decontaminated residues.
8.5.4 Other costs and benefits
A.
Human health benefits
722.
The human health
benefits associated with reductions of mercury in the biosphere have been
addressed in detail in chapter 4.
B.
Economic costs of mercury use, especially in products
723.
The purely economic
costs of dealing with the mercury in our products and our surroundings are
considerable, but describing them in detail is not within the scope of
this assessment. Nonetheless,
several examples are worth mentioning, such as: cost of collecting
separately mercury containing products; cost of recycling or acceptable
disposal, whether to a special landfill or to a hazardous waste
incinerator; cost of generating and enforcing legislation to deal with
mercury in every sector of the economy; cost of tracking movements of
mercury waste; cost of the extensive programmes in various countries (such
as around the Great Lakes region of the USA and Canada) to significantly
reduce mercury releases; cost of pursuing automobile companies to replace
mercury switches; cost of special controls on municipal waste incinerators
to remove mercury from the flue gases, etc.
All of these examples represent costs to the local, regional and
world economies that remain because mercury remains reasonably free to
move through the economy.
C.
Ecological and welfare benefits of reducing mercury pollution
724.
As an example of a
great variety of benefits that are often given little notice, it is
instructive to consider in some detail the ecological
and welfare benefits of reducing mercury pollution. As noted in US EPA (1997),
mercury can adversely affect ecological systems at various levels:
at the individual organism level, at the population level, and at the
community or ecosystem level. While
the effects on populations, communities, and ecosystems are of primary
concern for most species, individual effects are also of interest because
they may cause effects at higher levels of the ecological system,
especially effects in vulnerable or reduced populations such as threatened
and endangered species, raptors, and furbearers.
725.
Likewise, there is a
broad range of cultural and welfare benefits associated with
reductions in the global mercury load.
US EPA (1997) noted that the top three social and economic damages
to native peoples were (1) diminishment of cultural and religious values;
(2) damage to subsistence activities (e.g., subsistence fishing); and (3)
damage to natural resources in commercial use.
Fishing often plays a role in all three of these areas.
With respect to cultural values, for example, the Wisconsin Native
Americans have built centuries-old traditions around spearing fish and
sharing the catch. Growing
concerns about limiting fish consumption and limiting the locations where
fish may be caught seriously affect the Tribe's traditions (US EPA 1997).
726.
The Arkansas Game and
Fish Commission attempted to quantify fishing-related monetary losses due
to mercury contamination as of 1994.
Although the Commission has not published its findings (Armstrong
1994), it estimated a loss of fishing expenditures due to mercury fish
consumption advisories of over $US 5 million from 1991 to 1992.
This estimate was derived from decreased purchases of fishing
license in counties where mercury advisories were issued, multiplied by
the average number of trips an angler takes per year, and by the average
per-trip expenditures. Changes
in expenditures represent changes in welfare (US EPA 1997).
727.
Other than the work
cited above, little work has been done to quantify the value of most of
these ecological and welfare benefits,
which will vary greatly in any case from one region to another.
Therefore, the summary provided in table 8.17 below is presented
without any attempt at quantification.
Table
8.17 Summary of typical ecological/welfare benefits and the potential
adverse effect on them
from mercury pollution (from US EPA, 1997)
|
Ecological/welfare
benefit or use category
|
Adverse
effect of mercury pollution
|
|
Recreational
Fishing
|
-
Reduced number
of fishing trips
-
Lost value per
trip due to fish advisory
-
Lost
value due to inability to consume fish
|
|
Commercial
Fishing
|
|
|
Subsistence
fishing
|
|
|
Timber
|
|
|
Forest
recreational activities
|
|
|
Agricultural
|
|
|
Recreational/Commercial
Hunting/Trapping
|
|
|
Recreational
bird hunting
|
|
|
Bird/animal
viewing
|
|
|
Cultural/religious
value
|
|
|
Existence
value of specific species,
including option value, bequest value, scarcity value, in
addition to existence value
|
|
|
Biodiversity
|
|
|
Stewardship
value, including moral obligation to reduce harm to ecological
resources
|
|
|
Preservation
of ecosystem health, including maintaining the integrity of
predator/prey relationships
|
|
|