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以重庆烟煤为原料,采用碳化-活化-气相沉积工艺制备了变压吸附(PSA)浓缩CH_4/N_2中CH_4用的成型活性炭,考察了制备工艺条件对活性炭浓缩CH_4/N_2中CH_4效果的影响.用低温液氮吸附方法对活性炭的孔结构进行了表征.实验结果表明,制备的成型活性炭在单循环五步PSA过程的抽真空步骤可使CH_4的浓度较原料气提高20.0%(体积分数)左右.对浓缩效果为20%(体积分数)的AC-1活性炭进行了表征,其BET比表面积为580m~2/g,微孔孔容为0.14cm~3/g,孔径分布主要集中在2.0~4.0nm.

Shaped active carbon adsorbents using bituminous coal from Chonqing mine as raw material for concentrating methane from CH_4/N_2 mixtures were prepared by taking carbonization-activation-deposition process and the effect of the preparation conditions on the pressure swing adsorption (PSA) concentrating performance was studied.The micro-structure characterization of active carbon was investigated by low temperature liquid nitrogen adsorption method.Experimental results showed that the methane concentration had increased 20.0vol% at the vacuum stage of PSA process with five steps using the shaped active carbon prepared as absorbent.As for one of the shaped active carbon adsorbents which concentrating effect was 20vol%,its BET specific surface area was 580m~2/g,total micropore volume was 0.14cm~3/g and its pore diameter size distribution was mostly between 2.0 and 4.0nm.

参考文献

[1] Simone Cavenati;Carlos A. Grande;Alirio E, Eodrigues .Separation of Methane and Nitrogen by Adsorption on Carbon Molecular Sieve[J].Separation Science and Technology,2005(13):2721-2743.
[2] Olajossy A .[J].Chemical engineering Research and Design,2003,81(04):474.
[3] 周理;周亚平 .高表面活性炭变压吸附分离甲烷/氮气混合物的方法[P].中国:CN02117916.6,2002.
[4] 周理;周亚平 .垃圾焚烧炉耦合活化炉制备高表面活性炭的方法[P].中国:CN02117917.4,2002.
[5] 闫新龙,刘欣梅,乔柯,王有和,阎子峰.成型活性炭制备技术研究进展[J].化工进展,2008(12):1868-1872,1881.
[6] 李永锋,凌军,刘燕珍,薛行华.高比表面积活性炭研究进展[J].热带作物学报,2008(03):396-402.
[7] Laishuan Liu;Zhenyu Liu;Jianli Yang .Effect of preparation conditions on the properties of a coal-derived activated carbon honeycomb monolith[J].Carbon: An International Journal Sponsored by the American Carbon Society,2007(14):2836-2842.
[8] Almansa C;Molina S M;Rodriguez R F .[J].Microporous and Mesoporous Materials,2004,76(03):185.
[9] Maria J H .[J].Carbon,2005,43:944.
[10] Mora E;Blanco C;Pajares J A et al.[J].Journal of Colloid and Interface Science,2006,298(01):3410.
[11] Mine G;Levent A .[J].Microporous and Mesoporous Materials,2006,88:126.
[12] 辜敏;鲜学福;刘克万 等.吸附剂变压吸附浓缩性能测试及渗流实验装置[P].中国:CN201110847Y,2008.
[13] 王秀芳,张会平,肖新颜,陈焕钦.高比表面积活性炭研制进展[J].功能材料,2005(07):975-977,980.
[14] 张守玉,吕俊复,岳光溪,王洋.煤种及炭化条件对活性焦孔隙结构的影响[J].煤炭学报,2003(02):167-172.
[15] Pereira P R;Pires J M;Carvalho B .[J].Separation Science and Technology,2001,21:237.
[16] Cavenati S;Grande C A .[J].Adsorption-Journal of the International Adsorption Society,2005,11(01):549.
[17] 赵文艳.大同煤生产高吸附活性炭工艺条件的选择[J].科技情报开发与经济,2006(01):170-172.
[18] 许国斌;牛和三 .[J].新型碳材料,1988,4:122.
[19] 朱学栋,朱子彬,韩崇家,张成芳.煤中含氧官能团的红外光谱定量分析[J].燃料化学学报,1999(04):335-339.
[20] 李宝华,李开喜,吕春祥,吴东,凌立成.煤基炭材料结构的初步考察[J].煤炭转化,2001(04):68-70.
[21] Ruiz B;Parra J B;Pajares J A .[J].Journal of Analytical and Applied Pyrolysis,2006,75:27.
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