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5.4 GEOCHEMICAL SEQUESTRATION OF CARBON DIOXIDE<br />

Part I: Impac<strong>ts</strong> of Climate-related Geo<strong>en</strong>gineering on Biological Diversity<br />

CO2 is naturally removed from the atmosphere by the weathering (dissolution) of carbonate and silicate rocks,<br />

forming bicarbonates and other compounds. However, the process of natural weathering is very slow: CO2 is<br />

consumed at less than one hundredth of the rate at which it is curr<strong>en</strong>tly being emitted.306 It has therefore be<strong>en</strong><br />

proposed that, in order to combat climate change, the natural process of weathering could be artificially accelerated.<br />

There is a range of proposed techniques that include releasing calcium carbonate or dissolution produc<strong>ts</strong> of alkaline<br />

minerals into the ocean, or spreading abundant silicate minerals such as olivine307 over agricultural soils—as<br />

discussed below.<br />

5.4.1 Enhanced ocean alkalinity<br />

This proposed approach is based on adding alkaline minerals (e.g., carbonate or silicate308 rock) or their dissolution<br />

produc<strong>ts</strong> to the ocean in order to chemically <strong>en</strong>hance ocean storage of CO2; it also expected to buffer the ocean<br />

to decreasing pH, and thereby help to counter ocean acidification.309<br />

It has be<strong>en</strong> proposed that dissolution produc<strong>ts</strong> of alkaline minerals could be released into the ocean through a<br />

range of techniques that include: i) CO2-rich gases dissolved in sea water to produce a carbonic acid solution that<br />

is th<strong>en</strong> reacted with a carbonate mineral to form calcium and bicarbonate ions;310, 311, 312 ii) addition to the ocean of<br />

bicarbonate ions produced from the electrochemical splitting of calcium carbonate (limestone);313 and iii) addition<br />

of magnesium and calcium chloride sal<strong>ts</strong> from hydrog<strong>en</strong> and chlorine ions produced from the electrolysis of sea<br />

water to form hydrochloric acid which is th<strong>en</strong> reacted with silicate rocks.314<br />

For deploym<strong>en</strong>t for geo<strong>en</strong>gineering purposes, all of these techniques would require very large volumes of feedstock<br />

minerals, abundant (non-carbon) <strong>en</strong>ergy, water, and ext<strong>en</strong>sive associated operational infrastructure. Most proposals<br />

<strong>en</strong>visage the addition of material through a pipeline into the sea or indirectly through discharge into a river: h<strong>en</strong>ce<br />

constraining their application to coastal zones, and limiting the pot<strong>en</strong>tial for rapid dilution (thereby increasing<br />

the risk of local negative impac<strong>ts</strong> on ecosystems).<br />

Other proposals involve the direct addition of limestone powder315 or calcium hydroxide316 to the ocean from<br />

ships, thereby increasing flexibility with the sites of application and also pot<strong>en</strong>tially achieving much higher dilution<br />

rates (therby minimizing short-term pH spikes). Note that the manufacture of calcium hydroxide requires <strong>en</strong>ergy<br />

and releases CO2 (that would need to be captured and safely stored), although the overall process is theoretically<br />

capable of net uptake.<br />

Such processes undoubtedly could have high long term effectiv<strong>en</strong>ess, i.e. on geological timescales. However, for<br />

geo<strong>en</strong>gineering purposes, the maximum pot<strong>en</strong>tial effectiv<strong>en</strong>ess of g<strong>en</strong>eric <strong>en</strong>hanced alkalinity techniques (in terms<br />

of their radiative forcing) has be<strong>en</strong> estimated317 as very low, at ≤ 0.03 W m-2.. This value is less than 1% of the<br />

306 Uchikawa & Zeebe (2008).<br />

307 Schuiling & Krijgsman (2006).<br />

308 The weathering of calcium carbonate (CaCO3) by CO2 mostly produces bicarbonate ions and calcium ions; the weathering of<br />

magnesium silicate (olivine; Mg2SiO4) mostly produces bicarbonate ions, magnesium ions, and silicic acid (H4SiO4). In theory, the<br />

latter is more effici<strong>en</strong>t, absorbing four molecules of CO2 for each molecule of magnesium silicate, with pot<strong>en</strong>tial sequestration of 0.34<br />

tonnes of carbon for each tonne of olivine.<br />

309 Kheshgi (1995).<br />

310 Rau & Caldeira (1999).<br />

311 Caldeira & Rau (2000).<br />

312 Rau (2011).<br />

313 Rau (2008).<br />

314 House et al. (2007).<br />

315 Harvey (2008).<br />

316 Cquestrate (http://www.cquestrate.com/).<br />

317 Vaughan & L<strong>en</strong>ton (2011).<br />

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