The Calcium-Looping technology for CO2 capture: On the important roles of energy integration and sorbent behavior

被引:307
作者
Perejon, Antonio [1 ,2 ]
Romeo, Luis M. [3 ]
Lara, Yolanda [3 ]
Lisbona, Pilar [3 ]
Martinez, Ana [3 ]
Manuel Valverde, Jose [4 ]
机构
[1] Univ Seville, CSIC, Inst Ciencia Mat Sevilla, Seville 41092, Spain
[2] Univ Seville, Fac Quim, Dept Quim Inorgan, E-41071 Seville, Spain
[3] Univ Zaragoza, CIRCE Res Ctr Energy Resources & Consumpt, Zaragoza 50018, Spain
[4] Univ Seville, Fac Phys, E-41012 Seville, Spain
关键词
CO2; capture; CCS; Calcium Looping; Limestone; CAO-BASED SORBENT; ENHANCED HYDROGEN-PRODUCTION; POSTCOMBUSTION CO2; CARBON-DIOXIDE; POWER-PLANTS; CARBONATION/CALCINATION CYCLE; CALCINATION CONDITIONS; THERMAL-DECOMPOSITION; SELF-REACTIVATION; ECONOMIC-ANALYSIS;
D O I
10.1016/j.apenergy.2015.10.121
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The Calcium Looping (CaL) technology, based on the multicyclic carbonation/calcination of CaO in gas-solid fluidized bed reactors at high temperature, has emerged in the last years as a potentially low cost technology for CO2 capture. In this manuscript a critical review is made on the important roles of energy integration and sorbent behavior in the process efficiency. Firstly, the strategies proposed to reduce the energy demand by internal integration are discussed as well as process modifications aimed at optimizing the overall efficiency by means of external integration. The most important benefit of the high temperature CaL cycles is the possibility of using high temperature streams that could reduce significantly the energy penalty associated to CO2 capture. The application of the CaL technology in precombustion capture systems and energy integration, and the coupling of the CaL technology with other industrial processes are also described. In particular, the CaL technology has a significant potential to be a feasible CO2 capture system for cement plants. A precise knowledge of the multicyclic CO2 capture behavior of the sorbent at the CaL conditions to be expected in practice is of great relevance in order to predict a realistic capture efficiency and energy penalty from process simulations. The second part of this manuscript will be devoted to this issue. Particular emphasis is put on the behavior of natural limestone and dolomite, which would be the only practical choices for the technology to meet its main goal of reducing CO2 capture costs. Under CaL calcination conditions for CO2 capture (necessarily implying high CO2 concentration in the calciner), dolomite seems to be a better alternative to limestone as CaO precursor. The proposed techniques of recarbonation and thermal/mechanical pretreatments to reactivate the sorbent and accelerate calcination will be the final subjects of this review. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:787 / 807
页数:21
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