CO2 sequestration with magnesium silicates-Exergetic performance assessment

被引:19
|
作者
Romao, Ines [1 ,2 ]
Slotte, Martin [1 ]
Gando-Ferreira, Licinio M. [2 ]
Zevenhoven, Ron [1 ]
机构
[1] Abo Akad Univ, Thermal & Flow Engn Lab, Turku, Finland
[2] Univ Coimbra, Dept Chem Engn, Coimbra, Portugal
来源
关键词
CO2 mineral sequestration; Serpentinite; AS/ABS salt; Exergy; Energy efficiency; MINERALIZATION;
D O I
10.1016/j.cherd.2014.05.016
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A staged process for CO2 sequestration by mineralisation, using magnesium silicates, studied at angstrom bo Akademi (angstrom A) involves the production of magnesium hydroxide from suitable rock (requiring heat at similar to 350-450 degrees C) using recoverable ammonium salts and its subsequent carbonation (generating heat at similar to 500 degrees C). In addition, the process gives substantial amounts of solid by-products making the integration of mineral carbonation with other industries an opportunity to both reduce CO2 emissions and substitute raw material inputs. Aspen Plus (R) v7.2 software is used to optimize the AA process towards minimal energy use and to study the impact of the flue gases' CO2 concentration (conventional coal firing (CCF) vs. oxyfuel combustion (OXY) flue gases) in the carbonation step instead of pre-separated and compressed CO2 (providing an additional benefit compared to "conventional" CO2 capture and storage (CCS) options). Also the influence of using either ammonium sulphate (AS) or bisulphate (ABS) as the fluxing salts on the process's exergetics is evaluated. It was concluded that ABS lowers the energy requirements in the Mg extraction by 40% but its regeneration (fundamental feature for the route's success) by: (i) thermal decomposition of AS appears to be unviable, (ii) addition of H2SO4 saturates the process with sulphur. The simulation results showed that the extraction with ABS and carbonation with OXY flue gases requires less energy input. (C) 2014 The Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3072 / 3082
页数:11
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