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比表面积和吸附强度对TiO_2/活性炭复合体光催化降解酸性红27活性和动力学的影响 被引量:4
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作者 李佑稷 陈伟 李雷勇 《物理化学学报》 SCIE CAS CSCD 北大核心 2011年第7期1751-1756,共6页
通过超临界预处理和溶胶-凝胶过程,制备TiO_2/活性炭复合体(TCS),利用X射线衍射,X光电子能谱和氮气吸附-解吸分析对其结构特征进行表征,以酸性红27的光催化降解评价复合体的)光催化活性.结果表明:TCS光催化活性比纯TiO_2大,归功于TiO_2... 通过超临界预处理和溶胶-凝胶过程,制备TiO_2/活性炭复合体(TCS),利用X射线衍射,X光电子能谱和氮气吸附-解吸分析对其结构特征进行表征,以酸性红27的光催化降解评价复合体的)光催化活性.结果表明:TCS光催化活性比纯TiO_2大,归功于TiO_2小晶粒尺寸,对酸性红27和羟基自由基高的吸附量.TCS复合体对酸性红27的降解效率随其比表面积的增大先升高后降低.通过改进的Langmuir-Hinshelwood模型对睃性红27在不同的复合体上光催化降解动力学行为进行描述,表明TCS光催化活性的差异主要是由比表面积和吸附强度相互制约所引起.TCS3由于具有适当的比表面积和恰当的吸附强度而具有最高的光催化活性. 展开更多
关键词 光催化 氧化钛 超临界 溶胶-:动力学
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Zirconium Diboride Powders Synthesized by Boro/Carbothermal Reaction Using Sol-Gel Technology
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作者 季惠明 范红娜 +1 位作者 丰红军 孙晓红 《Transactions of Tianjin University》 EI CAS 2015年第3期228-233,共6页
A single phase of zirconium diboride (ZrB2) powder was successfully synthesized by sol-gel method in Zr-B-C-O system, using zirconium oxychloride (ZrOC12 ~ 8H20), nano-scale boron and suerose(C12H22011)as the st... A single phase of zirconium diboride (ZrB2) powder was successfully synthesized by sol-gel method in Zr-B-C-O system, using zirconium oxychloride (ZrOC12 ~ 8H20), nano-scale boron and suerose(C12H22011)as the starting materials and propylene oxide (PO) as complexing agent at a low temperature. Simultaneously, the experimen- tal and theoretical studies of ZrB2 synthesized by boro/carbothermal reduction from novel sol-gel technology were discussed. The results indicated that the pure rod-like ZrB2 powder without residual ZrO2 phase could be obtained with a B/Zr molar ratio of 3.5 at 1 400~C in argon atmosphere. Besides, in this study, a kinetic model for the Zr-B-C-O sys- tem producing ZrB2 by boro/carbothermal reaction was established based on thermodynamic analysis. It was also ob- served that, with the increase of reaction temperature, the reaction which produced ZrB2 powders changed from the borothermal reaction to boro/carbothermal reaction in the Zr-B-C-O system. 展开更多
关键词 zirconium diboride boro/carbothermal reaction kinetic model sol-gel method
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Photo oxidation of DBT using carbon nanotube titania composite as visible light active photo catalyst 被引量:1
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作者 BARMALA Molood BEHNOOD Mohammad OMIDKHAH Mohammad Reza 《Journal of Central South University》 SCIE EI CAS CSCD 2018年第7期1642-1650,共9页
Sulfur removal from liquid fuels has increased in importance in recent years. Although hydrodesulfurization is the usual method for removing sulfur, the elimination of thiophene compounds using this process is difficu... Sulfur removal from liquid fuels has increased in importance in recent years. Although hydrodesulfurization is the usual method for removing sulfur, the elimination of thiophene compounds using this process is difficult. Photocatalysis is an alternative method being developed for thiophene removal at ambient conditions. Among semiconductors, titania has shown good potential as a photo-catalyst; however, quick recombination of electron holes hinders its commercial use. One way to decrease the recombination rate is to combine carbon nanotubes with a semiconductor. In this work, multiwall carbon nanotube (MWCNT) / titania composites were prepared with different mass ratios of MWCNT to titania using tetraethyl orthotitanate (TEOT) and titanium tetra isopropoxide (TTIP) as precursors of titania. Dibenzothiophene (DBT) photocatalytic removal from n-hexane was measured in both the presence and absence of oxygen. The results indicated that the best removal occurred when the MWCNT to titania ratio was 1. When the ratio exceeded this number, DBT removal efficiency decreased due to light scattering. Also, the composites prepared by TEOT exhibited better efficiency in DBT removal. The research findings suggested that the obtained composite was a visible light active photocatalyst and exhibited better performance in the presence of oxygen. Kinetics of photocatalytic DBT removal was a first-order reaction with removal rate constant 0.7 h–1 obtained at optimum conditions. 展开更多
关键词 advanced oxidation processes carbon nanotube PHOTOCATALYSIS UV KINETICS SEMICONDUCTOR sol-gel process
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