Influence of oxidation upon the CO2 capture performance of a phenolic-resin-derived carbon

被引:47
作者
Plaza, M. G. [1 ]
Thurecht, K. J. [2 ,3 ]
Pevida, C. [1 ]
Rubiera, F. [1 ]
Pis, J. J. [1 ]
Snape, C. E. [4 ]
Drage, T. C. [4 ]
机构
[1] INCAR CSIC, Inst Nacl Carbon, Oviedo 33080, Spain
[2] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[3] Univ Queensland, Ctr Adv Imaging, St Lucia, Qld 4072, Australia
[4] Univ Nottingham, Dept Chem & Environm Engn, Fac Engn, Nottingham NG7 2RD, England
基金
英国工程与自然科学研究理事会;
关键词
Adsorption; Oxidation; Carbon materials; CO2; capture; ELECTRIC SWING ADSORPTION; ACTIVATED CARBON; FLUE-GAS; POSTCOMBUSTION CAPTURE; SURFACE COMPLEXES; DIOXIDE CAPTURE; SOLID SORBENTS; FIBER SURFACES; NITRIC-ACID; ADSORBENTS;
D O I
10.1016/j.fuproc.2013.01.011
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The effect of oxidation upon the CO2 capture performance has been studied taking a phenolic resin carbon as the base material. Oxygen surface groups were introduced through liquid and gas phase oxidation treatments, using ammonium persulfate, nitric acid and air, respectively. The surface chemistry of the final carbon is strongly affected by the type of oxidation treatment: liquid phase oxidation introduces a greater amount of oxygen, mostly as carboxylic groups; these are absent in the gas phase oxidised sample that contains mainly ether and carbonyl functionalities. The porous texture of the samples is also affected by the oxidation treatment: through liquid phase oxidation the pore volume is somewhat reduced, while this is slightly developed by air treatment at 693 K. Despite the reduction in the porous volume and the acidic surface, liquid-phase oxidised samples present greater CO2 adsorption capacity than the starting carbon due to Lewis acid-base interactions with the CO2 molecule. Moreover: oxidised samples are easily regenerated, and observed heats of adsorption are typical from physisorption processes, which will facilitate the adsorbent regeneration in cyclic adsorption processes. Oxidation is therefore proposed as a plausible modification technique for developing easy-to-regenerate carbon adsorbents with enhanced CO2 capture performance. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 60
页数:8
相关论文
共 64 条
[1]  
[Anonymous], 2010, Energy Technology Perspectives 2010
[2]  
Bandosz TJ, 2006, INTERFACE SCI TECHNO, V7, P1
[3]  
Bansal RC., 2005, ACTIVATED CARBON ADS, DOI 10.1201/9781420028812
[4]   Characterisation of surface oxides on carbon and their influence on dynamic adsorption [J].
Beck, NV ;
Meech, SE ;
Norman, PR ;
Pears, LA .
CARBON, 2002, 40 (04) :531-540
[5]   Strong Lewis acid-Lewis base interactions between supercritical carbon dioxide and carboxylic acids: Effects on self-association [J].
Bell, PW ;
Thote, AJ ;
Park, Y ;
Gupta, RB ;
Roberts, CB .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2003, 42 (25) :6280-6289
[6]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[7]   KINETICS OF CARBAMATE FORMATION AND BREAKDOWN [J].
CAPLOW, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1968, 90 (24) :6795-&
[8]  
Carson JK, 2000, J CHEM THERMODYN, V32, P1285
[9]   Adsorbent Materials for Carbon Dioxide Capture from Large Anthropogenic Point Sources [J].
Choi, Sunho ;
Drese, Jeffrey H. ;
Jones, Christopher W. .
CHEMSUSCHEM, 2009, 2 (09) :796-854
[10]   ESCA CHARACTERIZATION OF COMMERCIAL CARBON-BLACKS AND OF CARBON-BLACKS FROM VACUUM PYROLYSIS OF USED TIRES [J].
DARMSTADT, H ;
ROY, C ;
KALIAGUINE, S .
CARBON, 1994, 32 (08) :1399-1406