7 Seifritz W. CO2 disposal by means of silicates. Nature, 1990, 345: 486
[5]
8 Huijgen W J J, Witkamp G J, Comans R N J. Mechanisms of aqueous wollastonite carbonation as a possible CO2 sequestration process. Chem Eng Sci, 2006, 61: 4242-4251？？
[6]
20 Hernandez G M, Lopez R P, Renard F, et al. Mineral sequestration of CO2 by aqueous carbonation of coal combustion fly-ash. J Hazard Mater, 2009, 161: 1347-1354？？
[7]
21 Huntzinger D N, Gierke J S, Sutter L L, et al. Mineral carbonation for carbon sequestration in cement kiln dust from waste piles. J Hazard Mater, 2009, 168: 31-37？？
[8]
22 Rendek E, Ducom G, Germain P. Carbon dioxide sequestration in municipal solid waste incinerator (MSWI) bottom ash. J Hazard Mater,2006, 128: 73-79？？
[9]
23 Iizuka A, Fujii M, Yamasaki A, et al. Development of a new CO2 sequestration process utilizing the carbonation of waste cement. Ind Eng Chem Res, 2004, 43: 7880-7887？？
[10]
28 Liu J, Han Y, Wang Y. Potassium extraction from Potassium-rich shale by high pressure hydrothermal method. Min Metall, 2008, 4:31-37
[11]
29 Casey W H, Westrich R, Arnold G W. Surface chemistry of labradorite feldspar reacted with aqueous solutions at pH = 2, 3, and 12. Geochem Cosmochim Acta, 1988, 52: 2795-2806
[12]
30 Berg A, Banwart S A. Carbon dioxide mediated dissolution of Ca-feldspar: Implications for silicate weathering. Chem Geol, 2000, 163:25-42？？
[13]
1 Melt B, Davidson O, Connick H D, et al. Report on Carbon Dioxide Capture and Storage. Cambridge: Cambridge University Press, 2005
[14]
4 谢和平. 发展低碳技术、推进绿色经济. 中国能源, 2010, 32: 5-10
[15]
5 谢和平. CO2 矿化利用的CCU 新理念. 技术报告, 中国工程院能源与矿业学部, 2012
[16]
9 Koukouzas N, Gemeni V, Ziock H J. Sequestration of CO2 in magnesium silicates, in Western Macedonia, Greece. Int J Miner Process,2009, 93: 179-186？？
[17]
10 Daval D, Martinez I, Corvisier J, et al. Carbonation of Ca-bearing silicates, the case of wollastonite: Experimental investigations and kinetic modeling. Chem Geol, 2009, 265: 63-78？？
[18]
11 Valer M M M, Fauth D J, Kuchta M E, et al. Activation of magnesium rich minerals as carbonation feedstock materials for CO2 sequestration. Fuel Process Technol, 2005, 86: 1627-1645？？
[19]
12 Fagerlund J, Teir S, Nduagu E, et al. Carbonation of magnesium silicate mineral using a pressurized gas/solid process. Energy Procedia,2009, 1: 4907-4914？？
[20]
13 Kakizawa M, Yamasaki A, Yanagisawa Y. A new CO2 disposal process via artificial weathering of calcium silicate accelerated by acetic acid. Energy, 2001, 26: 341-354？？
[21]
14 Munz A I, Kihle J, Brandvoll O, et al. A continuous process for manufacture of magnesite and silica from olivine, CO2 and H2. Energy Procedia, 2009, 1: 4891-4898
[22]
15 Park A H A, Fan L S. CO2 mineral sequestration: Physically activated dissolution of serpentine and pH swing process. Chem Eng Sci,2004, 59: 5241-5247？？
[23]
16 Huijgen W J J, Comans R N J, Witkamp G J. Cost evaluation of CO2 sequestration by aqueous mineral carbonation. Energy Conv Manag,2007, 48: 1923-1935？？
[24]
17 Krevor S C, Lackner K S. Enhancing process kinetics for mineral carbon sequestration. Energy Procedia, 2009, 1: 4867-4871？？
[25]
18 O’conner W C, Dahlin D C, Rush G E, et al. Carbon dioxide sequestration by direct mineral arbonation: Process mineralogy of feed and products. Miner Metall Process, 2002, 19: 95-101
[26]
19 Huijgen W J J, Witkamp G J, Comans R N J. Mineral CO2 sequestration by steel slag carbonation. Environ Sci Technol, 2005, 39:9676-9682？？
[27]
24 IEA. CO2 Emission From Fuel Combustion Highlights. France: OECD/IEA, 2011
[28]
25 Xu T, Apps J A, Pruess K. Mineral sequestration of carbon dioxide in a sandstone-shale system. Chem Geol, 2005, 217: 295-318？？
[29]
26 Fu Q, Lu P, Konishi H, et al. Coupled alkali-feldspar dissolution and secondary mineral precipitation in batch systems: 1. New experiments at 200℃ and 300 bars. Chem Geol, 2009, 258: 125-135
[30]
27 马鸿文. 中国富钾岩石. 北京: 化学工业出版社, 2010
[31]
31 Oelkers E H, Schott J. Does organic acid adsorption affect alkali-feldspar dissolution rates? Chem Geol, 1998, 151: 235-245
[32]
32 Blake R E, Walter L M. Effects of organic acids on the dissolution of orthoclase at 80℃ and pH 6. Chem Geol, 1996, 132: 91-102？？
