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四乙基溴化铵相转移催化合成N,N-二乙基苯胺的研究 被引量:1
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作者 田庆伟 《精细化工》 CAS CSCD 1996年第5期44-47,共4页
在常压下以四乙基溴化铵作相转移催化剂合成制得N,N二乙基苯胺,研究了各反应因素对目的产物产率的影响,其优化工艺条件为:在50ml50%的氢氧化钠溶液中,苯胺和溴乙烷的摩尔比为1∶2,四乙基溴化铵用量为025g,6... 在常压下以四乙基溴化铵作相转移催化剂合成制得N,N二乙基苯胺,研究了各反应因素对目的产物产率的影响,其优化工艺条件为:在50ml50%的氢氧化钠溶液中,苯胺和溴乙烷的摩尔比为1∶2,四乙基溴化铵用量为025g,60℃下常压反应7h,产品产率为815%。 展开更多
关键词 四乙基溴化铵 相转换催化 二乙基苯胺 合成
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超声波作用下的糖精相转移催化N-苄基化反应的研究
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作者 嵇学林 刘华 黄昆 《化学研究与应用》 CAS CSCD 1997年第1期66-68,共3页
超声波作用下的糖精相转移催化N-苄基化反应的研究嵇学林刘华黄昆(江苏镇江医学院有机化学教研室镇江212001)关键词超声波相转换催化糖精苄基化有机声化学近年来,由于超声波(Ultrasoun,缩写U.S)在有机合成中... 超声波作用下的糖精相转移催化N-苄基化反应的研究嵇学林刘华黄昆(江苏镇江医学院有机化学教研室镇江212001)关键词超声波相转换催化糖精苄基化有机声化学近年来,由于超声波(Ultrasoun,缩写U.S)在有机合成中应用的不断发展,逐渐形成了一门新兴... 展开更多
关键词 超声波 相转换催化 糖精 苄基化
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利用相转移催化技术进行水玻璃的有机化
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作者 杨春生 稻垣慎二 冈本弘 《无机化学学报》 SCIE CAS CSCD 北大核心 1992年第1期58-61,共4页
本研究报告了在相转移催化剂存在下,水玻璃与有机锡化合物反应,可以得到高粘性液体产物。考察了各种条件对反应的影响,结果表明:水相的pH在一定范围内反应才能进行;有机溶剂种类对产物分子量的大小有明显影响;相转移催化剂的效率与过去... 本研究报告了在相转移催化剂存在下,水玻璃与有机锡化合物反应,可以得到高粘性液体产物。考察了各种条件对反应的影响,结果表明:水相的pH在一定范围内反应才能进行;有机溶剂种类对产物分子量的大小有明显影响;相转移催化剂的效率与过去报道的水-苯体系的结论相一致。 展开更多
关键词 水玻璃 有机化 有机锡 相转换催化
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Single‐atom catalysts on metal‐based supports for solar photoreduction catalysis 被引量:5
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作者 Huayang Zhang Wenjie Tian +4 位作者 Xiaoguang Duan Hongqi Sun Yingping Huang Yanfen Fang Shaobin Wang 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 2022年第9期2301-2315,共15页
Metal atoms atomically dispersed on an inorganic metal‐based support compose a unique category of single atom catalysts(SACs)and have important applications in catalytic photoreduction reactions,including H_(2) evolu... Metal atoms atomically dispersed on an inorganic metal‐based support compose a unique category of single atom catalysts(SACs)and have important applications in catalytic photoreduction reactions,including H_(2) evolution reaction,CO_(2) reduction reaction,and N_(2) reduction reaction.In this minreview,we summarized the typical metal‐support interaction(M‐SI)patterns for successful anchoring of single‐atom metals on metallic compound supports.Subsequently,the contribution of the dispersed single metal atoms and M‐SI to photocatalytic reactions with improved activity,selectivity,and stability are highlighted,such as by accelerating charge transfer,regulating band structure of the support,acting as the reductive sites,and/or increasing catalytic selectivity.Finally,some challenges and perspectives of future development are proposed.We anticipate that this minireview will be a beneficial supplement for a comprehensive perception of metal‐based material supported SACs and their application in heterogeneous photo‐reductive catalysis. 展开更多
关键词 Single atom catalyst Metal‐based support Metal‐support interaction PHOTOCATALYSIS Solar energy conversion
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Decoupling hydrogen production from water oxidation by integrating a triphase interfacial bioelectrochemical cascade reaction
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作者 Jun Zhang Xia Sheng +6 位作者 Zhenyao Ding Haili Wang Lai Feng Xiqi Zhang Liping Wen Lei Jiang Xinjian Feng 《Science Bulletin》 SCIE EI CSCD 2021年第2期164-169,M0004,共7页
Water electrolysis to produce H2 is a promising strategy for generating a renewable fuel.However,the sluggish-kinetics and low value-added anodic oxygen evolution reaction(OER)restricts the overall energy conversion e... Water electrolysis to produce H2 is a promising strategy for generating a renewable fuel.However,the sluggish-kinetics and low value-added anodic oxygen evolution reaction(OER)restricts the overall energy conversion efficiency.Herein we report a strategy of boosting H_(2)production at low voltages by replacing OER with a bioelectrochemical cascade reaction at a triphase bioanode.In the presence of oxygen,oxidase enzymes can convert biomass into valuable products,and concurrently generate H_(2)O_(2) that can be further electrooxidized at the bioanode.Benefiting from the efficient oxidase kinetics at an oxygen-rich triphase bioanode and the more favorable thermodynamics of H_(2)O_(2)oxidation than that of OER,the cell voltage and energy consumption are reduced by~0.70 V and~36%,respectively,relative to regular water electrolysis.This leads to an efficient H_(2)production at the cathode and valuable product generation at the bioanode.Integration of a bioelectrochemical cascade into the water splitting process provides an energy-efficient and promising pathway for achieving a renewable fuel. 展开更多
关键词 Hydrogen production Water electrolysis OXIDASE Bioelectrochemical cascade reaction
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