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Environmental Implications2
Environmental Implications2
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T H E S TAT E O F T H E D E B AT E
Keywords
automotive technology
batteries
electric vehicles
industrial ecology
lead
leaded gasoline
Summary
The lead battery has the potential to become one of the
first examples of a hazardous product managed in an environmentally acceptable fashion. The tools of industrial
ecology are helpful in identifying the key criteria that an
ideal lead-battery recycling system must meet: maximal recovery of batteries after use, minimal export of used batteries to countries where environmental controls are
weak, minimal impact on the health of communities near
lead-processing facilities, and maximal worker protection
from lead exposure in these facilities. A well-known risk
analysis of electric vehicles is misguided, because it treats
lead batteries and lead additives in gasoline on the same
footing and implies that the lead battery should be abandoned. The use of lead additives in gasoline is a dissipative
use where emissions cannot be confined; the goal of management should be and has been to phase out this use.The
use of lead in batteries is a recyclable use, because the lead
remains confined during cycles of discharge and recharge.
Here, the goal should be clean recycling.The likelihood that
the lead battery will provide peaking power for several
kinds of hybrid vehiclesa role only recently identified
increases the importance of understanding the levels of
performance achieved and achievable in battery recycling.
A management system closely approaching clean recycling
should be achievable.
Editors note: The debate over lead-acid batteries and electric vehicles
continues in the second issue of the Journal of Industrial Ecology with
a response to this article by Lave, Hendrickson and McMichael and a
rejoinder by Socolow and Thomas.
13
T H E S TAT E O F T H E D E B AT E
T H E S TAT E O F T H E D E B AT E
that the air emissions factor for secondary smelting (air emissions divided by lead production) is
about 0.03%, and, therefore, that about 3% of
all emissions are air emissions.4
Are total releases or air releases the more appropriate quantity to compare? The LRHM
analysis, while presenting both alternatives, prefers the use of total releases, on the grounds that
there is a potential for resuspension of fine particulate matter containing lead and the weathering and leaching of lead to air and water from
solid waste containing lead. . . . The total environmental discharges are the eventual burden,
even though air emissions pose the greatest immediate threat (Lave et al. 1996, 405, 406).
There is no discussion of how a future burden
becomes a future threat (how much lead might
be leached from slag and enter drinking water,
for example), or of whether future threats should
be discounted relative to present threats.
The LRHM analysis also quantifies the lead
emissions associated with the lead-acid startinglighting-ignition (SLI) battery that provides
starting power for todays cars. This battery is assumed to contain 8 kg of lead (40 times less than
the lead in the battery of the reference electric
vehicle) and to remain in the car for four years
(twice as long), so that 80 times as much lead
flows annually through an electric car with a lead
battery as flows through a car that contains lead
only in the SLI battery.5
The LRHM analysis concludes that the firstgeneration electric car powered by lead batteries
is a potential environmental liability, and implies that there is greater merit in pursuing the
gasoline-powered car with advanced pollution
control (Lave et al. 1996, 406). In the remainder
of this article, we take issue with this way of
framing the discussion. In section III we argue
that it is too early to remove the lead battery
from the list of technological options: the lead
battery may have several roles in future electric
vehicles, not only the role discussed in the
LRHM analysis. In section IV we argue, further,
that there is reason for optimism that an environmentally responsible management system for
lead batteries can be achieved. Quite generally,
opportunities for creative policymaking are uncovered when it is widely agreed that choices
among technologies can be made in more than
15
T H E S TAT E O F T H E D E B AT E
one step (Ross and Socolow 1991). With constructive initatives coming from several directions, a potential environmental liability does
not have to become a real one.
T H E S TAT E O F T H E D E B AT E
17
T H E S TAT E O F T H E D E B AT E
T H E S TAT E O F T H E D E B AT E
25
A)
NHANES II
20
Persons, %
15
10
5
0
25
NHANES III
Persons, %
20
B)
15
10
5
0
0
0.10 0.19 0.29 0.39 0.48 0.58 0.68 0.77 0.87 0.97 1.06 1.16 1.25 1.35 1.45
(2) (4) (6) (8) (10) (12) (14) (16) (18) (20) (22) (24) (26) (28) (30)
Blood Lead Level, mol/L (g/dL)
Children, %
20
NHANES II
C)
NHANES III
D)
15
10
5
0
Children, %
20
15
10
5
0
0
0.10 0.19 0.29 0.39 0.48 0.58 0.68 0.77 0.87 0.97 1.06 1.16 1.25 1.35 1.45
(2) (4) (6) (8) (10) (12) (14) (16) (18) (20) (22) (24) (26) (28) (30)
Blood Lead Level, mol/L (g/dL)
Figure 1 Histograms of blood lead levels in two national samples, the National Health and Nutrition
Examination Surveys known as NHANES II and NHANES III, roughly a decade apart. The data in
NHANES II are from 1976 to 1980 and the data in NHANES III are from 1988 to 1991. Both the full
samples (A, B) and the subsamples of children aged 1 to 5 (C, D) are shown. The units of blood lead level
are given in both micromoles per liter and micrograms per deciliter, two units which differ by a factor of
20.7 (one-tenth the atomic weight of lead). Source: Pirkle et al. (1994).
Socolow and Thomas, Industrial Ecology of Lead and EVs
19
T H E S TAT E O F T H E D E B AT E
T H E S TAT E O F T H E D E B AT E
400
400
US Use
Rest of OECD+Eastern Europe Use
Rest of the World Use
300
300
World Production
200
200
100
100
1940
1950
1960
1970
1980
0
1990
Year
Figure 2 A 50-year view of global production and consumption of lead in gasoline additives. Main
sources: International Lead and Zinc Study Group (1992); Octel (19701992).
21
T H E S TAT E O F T H E D E B AT E
during the 1970s and 1980s (U.S. Environmental Protection Agency 1993). As lead in gasoline
was reduced, U.S. air lead levels fell correspondingly. In 1979 the average concentration of lead
in urban air was 0.8 g/m3, and it was less than
0.1 g/m3 in 1988 (U.S. Environmental Protection Agency 1990).13
Studies of the effect of reduced use of lead in
gasoline on population blood lead levels have
been conducted in several other countries. In all
cases, decreased use of lead in gasoline results in
decreased blood lead levels. In three separate European studies, the average lead concentration in
blood fell by 6 to 9 g/dL when the lead concentration in gasoline was reduced from about 0.40
to 0.15 g/L. These studiesin Turin, Italy (Bono
et al. 1995), in Belgium (Ducoffre, Claeys, and
Bruaux 1990), and in Tarragona Province, Spain
(Schuhmacher et al. 1996)were conducted
over intervals of four to eight years. They also
measured substantial reductions in lead concentrations in air.
Although the drop in blood lead level is
highly correlated with the drop in use of lead in
gasoline, some of the decline may be attributable
to reductions in other sources of lead exposure,
including lead solder in canned foods and lead in
paint (Thomas 1995). In Christchurch, New
Zealand, a drop in average blood lead concentration of about 7 g/dL over about a four-year interval was seen, even though the concentration
of lead in gasoline remained constant at 0.84 g/L
and the volume of gasoline sold hardly changed
(Hinton et al. 1986). The authors of the New
Zealand study attributed the decrease in blood
lead levels to the fall in dietary and domestic
and industrial environmental sources of lead and
increasing public awareness of its effects.
Insight into the contribution of leaded gasoline to blood lead levels can be obtained with the
help of isotopic techniques. The stable isotopes
of lead (particularly 204, 206, 207, and 208) are
present in different ratios in different lead ores. If
the lead used in gasoline has isotopic ratios sufficiently different from the ratios for other sources
of lead exposure, then by measuring the isotopic
ratios of lead in the blood, gasoline, and other
sources, the fraction resulting from lead in gasoline can be determined. For a 1970s study in
Turin, Italy, the lead used in gasoline was
22
switched to a lead with isotopic ratios significantly different from the other local sources.
(The switchover was phased in over a period of
20 months, and the isotopically distinct gasoline
remained for an additional 31 months.) Before,
during, and after the switch, lead isotope ratios
were measured in blood and air. The results
showed that the portion of blood lead attributable to gasoline emissions (except for emissions
before the isotopically distinct gasoline was introduced) was approximately 5 g/dL out of
about 20 g/dL (Faccetti 1984, U.S. Environmental Protection Agency 1983).
The isotope technique provides only a lower
bound to the contribution of gasoline lead to
blood lead. At a later date (as mentioned above),
between 1985/86 and 1993/94, gasoline lead concentrations in Turin were reduced from 0.40 g/L
to 0.15 g/L, and average blood levels dropped
from 15.1 g/dL to 6.4 g/dL (Bono et al. 1995),
a larger drop than the isotope study would have
predicted. Part of the observed difference in the
blood lead levels before and after the reduction of
the lead concentration in gasoline may have
been a result of reduced exposure to other sources
of lead. And part may have been a result of an
underestimate of the portion of blood lead attributable to gasoline in the isotope experiment: lead
from gasoline used before the switchover may still
have been stored in bone and may not have fully
equilibrated with lead in blood (Schwartz 1996),
and lead from gasoline used before the switchover
may have been stored in soils and dust and inhaled or ingested after the switchover.
The evidence of these and other studies has
led to widespread recognition of leaded gasoline
as a significant contributor to human lead exposure. Where lead has been eliminated from gasoline, it is properly viewed as a major achievement.
Lead in Batteries
The ratio of secondary (recycling) lead production to primary lead production has increased nearly continuously in the United States
for the past 80 years. Figure 3 shows the details
of production during that period, as well as lead
consumption, by category of lead product, for
the past 30 years. Primary lead production has
fallen steadily since 1970, along with the total
T H E S TAT E O F T H E D E B AT E
1500
1000
500
0
1910
1930
1950
1970
1990
Year
Primary Production
Batteries
Secondary Production
Gasoline Additives
Net Imports
Figure 3 History of U.S. lead production and consumption. Production is in three categories, shown
additively: primary, secondary (recycled), and net imported lead. Consumption is in five categories, also shown
additively: batteries; gasoline additives; oxides for paints, glass, etc.; ammunition; and other products. Note that
gasoline additives, oxides, and ammunition are largely dissipative (most of the lead leaves the industrial
system with use), and that since 1970 the drop in primary production has approximately matched the drop
in total consumption for dissipative use. Note also that secondary production climbs with the increased
consumption of lead batteries. Sources: U.S. Bureau of Mines (1993, 1995); U.S. Department of Commerce
(1975, 603); Woodbury, Edelstein, and Jasinski (1993).
use of dissipative lead products (gasoline additives, oxides, and ammunition). Secondary lead
production in the same period closely tracks production of batteries.
The dominance of batteries and battery recycling in the lead flows through the U.S. economy
is seen in figure 4, which shows sources, products,
and fates. The total annual U.S. lead consumption (averaged over 1993 and 1994), about 1.4
million metric tons, is dominated by 910,000 metric tons of secondary (recycled) production, the
rest being primary production and imports. Batteries are the main product, consuming 1,180
thousand metric tons.
23
T H E S TAT E O F T H E D E B AT E
disposal from secondary lead recycling and battery manufacture in the United States. To conform to RCRA regulations, the slag that is the
solid aggregate remaining from the smelting process can be treated to reduce the ability of lead
to be leached. In a common method of treatment, called stabilization, leachability is reduced by mixing the waste with portland cement
(Lebo 1996).
Figure 4 also shows that about 50,000 metric
tons of lead are in batteries that are not recycled
but remain in the United States. Some of these
batteries end up in landfills, where leaching can
result in lead moving into groundwater or surface
water. As of the mid-1980s, battery lead was estimated to represent 65% of the total lead in municipal waste landfills (Franklin Associates
1988). The concentration of lead in leachate
from municipal waste landfills has been measured, and has been found to be as high as 1,600
micrograms of lead per liter of leachate (g/L) for
pre-1980 landfills, and as high as 150 g/L for
post-1980 landfills. The U.S. Environmental
Protection Agency presents a worst case scenario,
where this leachate is diluted by a factor of only
100 by groundwater before reaching well-water
(U.S. Environmental Protection Agency 1991).
The resulting maximum lead concentration in
drinking water from a pre-1980 landfill, 16 g/L,
can be compared with the current U.S. Safe
Drinking Water Act goal to reduce lead concentrations in drinking water to below 15 g/L.
Some unrecycled batteries do not go to landfills, but are discarded directly on the land (in
backyards, for example). Although lead is quite
immobile in soil and tends to be adsorbed by soil
particles, the lead in a battery discarded on the
land is relatively mobile; this is because up to half
of the lead in a battery is in the form of a paste of
lead oxide and lead sulfate, and because the acid
electrolyte can enhance lead migration in soil
(U.S. EPA 1991).
Figure 5 summarizes the record from 1975 to
1990 for the United States, showing the consumption of lead in gasoline additives and batteries, along with the average blood lead levels
in the population. The use of lead in batteries
has increased, although not steadily, and lead in
automotive gasoline has disappeared, while
population blood lead levels have plummeted.
Figure 4 Flows of
lead through the U.S.
economy in 199394.
(Data displayed are
averages of data for
1993 and 1994, in
thousands of metric
tons of lead per year.)
Other products are
bearings, brass, bronze,
cable covering, caulking
lead, casting materials,
pipes, and sheet lead.
Emissions to water or
airthe primary health
concernsare not
shown because they
are too small to be
visible at this scale. Also
not shown is the
roughly 0.6 thousand
metric tons of lead
used in aviation
gasoline (about a billion
liters with a lead
concentration of 0.4
0.8 grams per liter).
Sources: Battery Council
International (1995);
U.S. Bureau of Mines
(1995); U.S. Department of Commerce
(1994), U.S. Environmental Protection
Agency (1994a).
from mines
primary production
350
recycled
910
sources
current recycling
recycling waste: 7
products
total consumption
thousand metric
tons/yr
1410
batteries
1180
future recycling at
end of product life
fates
some recycled
unrecycled batteries: 50
recycled batteries
990
other: 95
oxides: 64 (for ceramics, paints, etc.)
ammunition 64
solder:13
(time lag)
~ 3 years
to landfills, etc.
to soil
to landfills, etc.
to landfills, etc.
to landfills, etc.
T H E S TAT E O F T H E D E B AT E
25
T H E S TAT E O F T H E D E B AT E
800
10
600
Batteries
400
5
200
g/dL
15
1000
1200
Gasoline
1976
1978
1980
1982
1984
1986
1988
1990
1992
Year
Gasoline
Batteries
Blood Lead
Figure 5 Annual U.S. lead use in gasoline and batteries and U.S. population blood lead levels from 1975
to 1990. Battery data are from U.S. Bureau of Mines 1993 and 1995. Gasoline data are from Nriagu 1990.
Both the battery and the gasoline data are referenced to the x-axis: they are not shown additively. Blood
lead data are from NHANES-II (Annest et al. 1983) and NHANES-III (Pirkle et al. 1994). NHANES-II data
are 28-day averages from February 1976 to February 1980 (Annest et al. 1983, figure 1). The single
NHANES-III blood-lead data point at 1990 is an average for 1988 to 1991. The dotted line connecting the
NHANES II time series with the single NHANES III data point is a only a guide to the eye: there are no
intermediate data points.
26
T H E S TAT E O F T H E D E B AT E
27
T H E S TAT E O F T H E D E B AT E
10
9
Number of Smelters
8
7
6
5
4
3
2
1
0
0.00030.001%
0.0010.003%
0.0030.01%
0.010.03%
T H E S TAT E O F T H E D E B AT E
Conclusions
The LRHM analysis has been productive, because it has called attention to the prospect that
serious negative environmental impacts could
result from the use of large amounts of lead in
the power sources of electric vehicles. But as a
guide to how to think about that prospect, the
LRHM analysis has three serious shortcomings.
First, as a technology assessment, it is oversimplified. It gives little weight to the ferment in
automotive engineering and, thereby, underestimates what is at stake in keeping open a multiplicity of technological options. Second, as a risk
assessment, it is misleading. It fails to identify
several critical environmental and public health
hazards associated with relatively small mass
flows, thereby demonstrating the perils of performing a mass-flow analysis without an accompanying hazard analysis. Third, as a guide to
industrial initiative and public policy, it is incomplete. It fails even to consider the possibility
that the lead-battery industry could implement a
model clean recycling system.
This is a period of great fluidity in automotive
engineering. Multiple options for providing the
energy for vehicles are being explored, and each
new capability has implications for several options at once. The battery-powered car could not
penetrate even niche markets at this time, if it
did not incorporate innovations related to fuel
economy and the management of electricity on
boardinnovations that have broad implications affecting the rates of progress for other vehicle concepts. The research-and-development
process would be proceeding more slowly, if state
and national governments were not actively promoting electric and hybrid vehicles through the
mandating of prototype development and pilotscale marketing.
An important argument against thwarting the
development of the lead battery for electric vehicles is that the lead battery may have a second,
entirely different, and potentially more important assignment than the assignment envisioned
in the LRHM analysis. In addition to providing
stand-alone power for short-range vehicles, the
lead battery may provide peak power in several
kinds of hybrid vehicles. These peak-power hybrids may be particularly suited to address, simultaneously, urban air quality, oil security, and
global warming. The fuel-cell/battery peakpower hybrid, in particular, may expand options
for the global transportation system by facilitating the introduction of renewable fuels.
When a social experiment is dangerous to the
public even at a small scale, it is important that it
be deterred. But there is another class of experiments, of which the pilot programs for electric
vehicles are an example, where the experiment
itself presents negligible risks, but full-scale
implementation has the potential for serious
harm. For this class of experiments, there may be
a large societal and environmental cost in suppressing the experiment. Freeman Dyson captures
what is at stake in an essay entitled, The Cost of
Saying No: It is not enough to count the hidden costs of saying yes to new enterprises. We
must also learn to count the hidden costs of saying no. . . . It often happens in technological development that one design turns out to be not
merely better but enormously better than its competitors, for reasons that could not have been predicted in advance. There is no way to find the
best design except to try out as many designs as
possible and discard the failures (Dyson 1975).
Because the LRHM analysis focuses on mass
flows rather than on hazards, it is poorly
matched to the task of identifying a recycling
systems most important environmental and
public health consequences. Often, on a mass
basis, the principal emissions are in the form of
29
T H E S TAT E O F T H E D E B AT E
Acknowledgments
We wish to thank Mark Baumgartner, L. Pasha Dritt, James J. Fanelli, and Margaret
Steinbugler for research assistance. We have
T H E S TAT E O F T H E D E B AT E
2.
3.
4.
5.
6.
Notes
1. Clean recycling has a dynamic dimension as well,
given that product demand varies over time. For
several decades the lead recycling system has managed the starting-lighting-ignition (SLI) battery
that provides starting power for gasoline-powered
vehicles. The system has grown to a global scale of
more than a hundred million recycled batteries per
year. A clean recycling system must assure that the
mining and primary processing of the lead required
to provide for an increasing stock of lead products
is conducted in environmentally responsible ways.
It must also assure environmentally responsible
contraction. Although no successor to the SLI battery is in view, some day a competitive alternative
might challenge its domination. Battery lead in
cars on the road would no longer have a predict-
31
7.
8.
9.
10.
32
T H E S TAT E O F T H E D E B AT E
11.
12.
13.
14.
T H E S TAT E O F T H E D E B AT E
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