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一锅法合成CexZr1-xO2固溶体催化剂用于热化学循环分解CO2制CO
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作者 施衡 雒京 +6 位作者 蒲彦锋 王峰 李枫 陈志文 宋权斌 肖福魁 赵宁 《燃料化学学报》 EI CAS CSCD 北大核心 2019年第11期1386-1393,I0007,共9页
采用一锅蒸发诱导自组装法(EISA)制备了一系列不同铈锆物质的量比的铈锆固溶体催化剂,用TGA研究了其热化学循环分解CO2制CO的催化性能,并采用XRD、Raman光谱、H 2-TPR、XPS、SEM和N 2吸附-脱附等手段对催化剂的物相结构、还原性能和表... 采用一锅蒸发诱导自组装法(EISA)制备了一系列不同铈锆物质的量比的铈锆固溶体催化剂,用TGA研究了其热化学循环分解CO2制CO的催化性能,并采用XRD、Raman光谱、H 2-TPR、XPS、SEM和N 2吸附-脱附等手段对催化剂的物相结构、还原性能和表面化学性质进行了表征分析,用热重分析(TGA)研究了铈锆固溶体对热化学循环分解CO2制CO的催化性能。结果表明,随着Ce/Zr物质的量比增加,铈锆固溶体催化剂的CO2高温分解活性先增大后减小。Ce/Zr物质的量比为1的Ce 0.5 Zr 0.5 O2催化剂由于具有较多的晶格缺陷和氧空穴,氧迁移能力强,催化活性高,而Ce/Zr物质的量比为3的Ce 0.75 Zr 0.25 O2催化剂具有相对稳定的氧空穴数,循环稳定性好。循环反应后,所有的催化剂均出现了一定程度的烧结,且富锆固溶体发生了相分离,这可能会影响催化剂的性能。 展开更多
关键词 CexZr1-xO2 CO2分解 热化学循环 氧空穴
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Macro kinetics for synthesis of dimethyl carbonate from urea and methanol on Zn-containing catalyst 被引量:1
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作者 ZHAO Wen-bo HAN Bing +2 位作者 ZHAO Ning xiao fu-kui WEI Wei 《Journal of Central South University》 SCIE EI CAS 2012年第1期85-92,共8页
In a stainless steel autoclave,the synthesis kinetics of dimethyl carbonate(DMC) from urea and methanol was separately investigated without catalyst and with Zn-containing catalyst.Without catalyst,for the first react... In a stainless steel autoclave,the synthesis kinetics of dimethyl carbonate(DMC) from urea and methanol was separately investigated without catalyst and with Zn-containing catalyst.Without catalyst,for the first reaction of DMC synthesis(the reaction of urea with methanol to methyl carbamate(MC)),the reaction kinetics can be described as the first order with respect to the concentrations of both methanol and urea.For the second reaction of DMC synthesis(the reaction of MC with methanol to DMC),the results exhibit characteristics of zero-order reaction.For Zn-containing catalyst,the first reaction is neglected in the kinetics model since its rate is much faster than the second reaction.The macro-kinetic parameters of the second reaction are obtained by fitting the experimental data to a pseudo-homogenous model,in which a side reaction in forming process of DMC is incorporated since it decreases the yield of DMC drastically at high temperature.The activation energy of the reaction from MC to DMC is 104 kJ/mol while that of the side reaction of DMC is 135 kJ/mol.The highest yield of DMC is 23%. 展开更多
关键词 macro-kinetics dimethyl carbonate UREA METHANOL methyl carbamate
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