Reactivity of CaO derived from nano-sized CaCO3 particles through multiple CO2 capture-and-release cycles

被引:140
作者
Florin, Nicholas H. [1 ]
Harris, Andrew T. [1 ]
机构
[1] Univ Sydney, Sch Chem & Biomol Engn, Lab Sustainable Technol, Sydney, NSW 2006, Australia
基金
澳大利亚研究理事会;
关键词
Calcium oxide; CO2; capture; sorbent; Nanostructure; Adsorption; Chemical processes; Environment; Particulate processes; CARBON-DIOXIDE; CALCIUM-OXIDE; PRODUCT LAYER; REACTIVATION; TEMPERATURE; CALCINATION; CAPACITY; SORBENT; BIOMASS;
D O I
10.1016/j.ces.2008.10.021
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The carbonation characteristics of pure CaO derived from nano-sized CaCO3 were investigated as part of a multi-cycle performance study which showed potential for exploiting the properties of nano-sized CaO sorbents in a continuous CO2 capture-and-release process. To help understand the approach to the decay asymptote, which is established through Multiple capture-and-release cycles, a qualitative model was proposed. The rate of approach and residual conversion defined by the decay asymptote represents the establishment of an equilibrium between the pore volume and surface area loss during thermal sintering: and the Pore Volume and surface area regeneration as a consequence of a solid-state diffusion mechanism, and the Subsequent release of CO2 in the next calcination cycle. This qualitative explanation is valid for all CaO derived CO2 sorbents. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:187 / 191
页数:5
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