Capturing CO2 from ambient air - David Keith
Capturing CO2 from ambient air - David Keith
Capturing CO2 from ambient air - David Keith
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value is based on a system built with existing technology and no optimization for the purpose of being<br />
most defensible on feasibility terms. It is an inelegant and inefficient design by any other measure. To<br />
illustrate this point, we applied a few obvious improvements to get a more efficient, if less defensible,<br />
design. This reduces the total cost by 40%. We would expect that, with the decade or more of serious<br />
technological development that would likely precede the deployment of <strong>air</strong> capture, much more drastic<br />
improvements would be made.<br />
But this analysis also suggests caution against exuberance for low-cost <strong>air</strong> capture. Even the improved<br />
system, at 140 $/t-<strong>CO2</strong> is far more costly than most conventional mitigation options. CCS <strong>from</strong> power<br />
plants is more likely around 30 $/t-<strong>CO2</strong>, and <strong>CO2</strong> emissions credits on the European market are currently<br />
trading for less than that. Air capture still may be a significant savings over switching to hydrogen cars<br />
(<strong>Keith</strong> and Farrell, 2003), but perhaps not over cellulosic ethanol (Morrow et al., 2006) as a means of<br />
removing carbon <strong>from</strong> the transportation sector. Some early claims about the cost of calcination-based <strong>air</strong><br />
capture were even lower than our lower-bound estimate of 60 $/t-<strong>CO2</strong>, which is partly why we included<br />
it. We don’t expect <strong>air</strong> capture will ever be competitive with capture <strong>from</strong> point sources. If it were, our<br />
lower bound calculation suggests it would have to be based on a process other than calcination.<br />
Yet the unique features of <strong>air</strong> capture – the potential for negative emissions and the backstop it provides<br />
on the cost of carbon mitigation – mean that even at a high price like 140 $/t-<strong>CO2</strong>, it is important for climate<br />
policy. <strong>Keith</strong> et al. (2006) demonstrated this with a long run global economic model, and the results make<br />
sense: <strong>air</strong> capture reduces the total social cost of mitigation. It guards against high carbon costs, and to<br />
some extent, against damage in extreme climate scenarios. By acting as a hedge against low probability,<br />
high-damage climate scenarios, it also shifts relatively more emissions reduction to the future. In a sense,<br />
fewer cautionary controls are needed on emissions when we know that <strong>air</strong> capture can be used to reduce<br />
atmospheric concentrations in case of emergency. As Parson (2006) points out, it is the classic “moral<br />
hazard” of insurance. But the danger is not so much that society, in maximizing total discounted social<br />
welfare, chooses to emit slightly more <strong>CO2</strong> in the near future, as that opponents of <strong>CO2</strong> regulation will use<br />
<strong>air</strong> capture as a political argument against action on the climate problem. If successful these arguments<br />
could lead to near term emissions far higher than optimum <strong>from</strong> a social welfare perspective.<br />
This is indeed a point of which <strong>air</strong> capture proponents should be wary. And the results of this analysis<br />
should serve as a reminder that, while <strong>air</strong> capture is feasible, the cost could be very high. At 250 $/t-<strong>CO2</strong>,<br />
<strong>air</strong> capture is best viewed as an option for use in only the direst of climate emergencies and should be little<br />
comfort for present-day emitters.<br />
In any case, this analysis supports the view that <strong>air</strong> capture is a serious option worthy of continued<br />
research. We have suggested many avenues for improving the design and finding lower cost versions<br />
of a NaOH-contactor-based <strong>air</strong> capture system. Additionally, we suggest that longer-term research into<br />
new recovery mechanisms and new sorbents – to break the thermodynamic constraints of calcination or<br />
hydroxide solutions, respectively – may yield the really dramatic cost reductions that would bring <strong>air</strong><br />
capture into widespread use.<br />
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