Adsorption-based process modelling for post-combustion CO2 capture

被引:12
|
作者
Plaza, M. G. [1 ]
Duran, I. [1 ]
Rubiera, F. [1 ]
Pevida, C. [1 ]
机构
[1] CSIC, Inst Nacl Carbon, INCAR, Apartado 73, E-33080 Oviedo, Spain
关键词
combustion CO2 capture; adsorption; N-2; ADSORPTION; POWER-PLANT; FLUE-GAS; TECHNOLOGY; ADSORBENTS; SIMULATION; PROJECT;
D O I
10.1016/j.egypro.2017.03.1365
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The EU FP7-funded HiPerCap project aims to develop novel post-combustion CO2 capture technologies and processes which are environmentally benign and have high potential to lead to breakthroughs in energy consumption and overall cost. Three different separation technologies are being evaluated on a fair basis: absorption, membranes and adsorption. In this work, some of the results related to the development of adsorption-based fixed bed systems are presented. The design and optimization of a multibed adsorption-based separation process requires the use of powerful simulators that can describe the non-steady state process. However, prior to use a mathematical model for process design this should be validated against experimental data. A VTSA experiment has been carried out in order to provide information on the cyclic performance of a microporous biochar. The working capacity of the adsorbent is reduced due to incomplete regeneration during cyclic operation, although it stabilizes at 0.5 mol CO2 kg(-1) and 0.4 mol H2O kg(-1) once cyclic steady state is reached. A non-isothermal non-adiabatic dynamic model of the VTSA cycle was built in Aspen Adsorption, which makes use of the Ideal Adsorbed Solution theory to account for competitive adsorption between N-2, CO2 and H2O. The model satisfactorily describes the history of the temperature of the adsorbent, the pressure, the total mass flow rate of the effluent, and the working capacity at cyclic steady state of the VTSA experiment. The validated model will be used as a starting point for process development. (c) 2017 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:2353 / 2361
页数:9
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