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固体酸SO_4^(2-)/SnO_2催化转化葡萄糖制备乙酰丙酸丁酯 被引量:8
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作者 刘娣 林鹿 +1 位作者 曾珊珊 彭林才 《林产化学与工业》 EI CAS CSCD 北大核心 2013年第2期66-70,共5页
以沉淀-浸渍法合成的SO24-/SnO2固体酸为催化剂,于丁醇体系中催化葡萄糖转化合成乙酰丙酸丁酯。考察了不同反应条件以及催化剂的重复利用性对产物得率的影响,并利用XRD和NH3-TPD对使用前后的催化剂的结构和酸性进行了表征。实验结果表明... 以沉淀-浸渍法合成的SO24-/SnO2固体酸为催化剂,于丁醇体系中催化葡萄糖转化合成乙酰丙酸丁酯。考察了不同反应条件以及催化剂的重复利用性对产物得率的影响,并利用XRD和NH3-TPD对使用前后的催化剂的结构和酸性进行了表征。实验结果表明:当催化剂于500℃焙烧3 h,用量2.5%,反应温度200℃的条件下反应2 h时,乙酰丙酸丁酯的得率最高达33.1%(摩尔得率,下同);回收利用的催化剂经过焙烧后使用催化性能有所下降,由最初的33.1%下降至回用5次后的12.8%。XRD和NH3-TPD分析结果表明,使用后催化剂的晶型结构仍保留,但酸强度和总酸量随重复使用次数增加却逐渐降低。 展开更多
关键词 固体酸so42- sno2 葡萄糖 乙酰丙酸丁酯 催化
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复合型固体超强酸SO_4^(2-)/SnO_2-TiO_2催化合成乙酸松油酯的研究 被引量:11
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作者 赵黔榕 吴春华 +3 位作者 毕韵梅 姜婧 石睿 秦红艳 《化学研究与应用》 CAS CSCD 北大核心 2006年第5期510-514,共5页
采用溶胶一凝胶法制备了新型复合固体超强酸SO42-/SnO2-TiO2,通过XRD和IR对其结构进行了表征。以该固体酸为催化剂、松油醇和乙酸酐为原料合成乙酸松油酯,考察了影响反应的因素。结果表明:反应温度40-50℃、催化剂用量1.8-2.2%、醇酐摩... 采用溶胶一凝胶法制备了新型复合固体超强酸SO42-/SnO2-TiO2,通过XRD和IR对其结构进行了表征。以该固体酸为催化剂、松油醇和乙酸酐为原料合成乙酸松油酯,考察了影响反应的因素。结果表明:反应温度40-50℃、催化剂用量1.8-2.2%、醇酐摩尔比1:1.6、反应时间4-5h是最适宜的反应条件,其松油醇转化率达到98%以上,产物中乙酸松油酯含量为88%。与普通单氧化物固体酸比较,该复合型固体酸有更高的催化活性和选择性。 展开更多
关键词 固体超强酸 ^so4^2-/sno2-TiO2 改性 乙酸松油酯 催化 合成
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固体超强酸SO_4^(2-)/SnO_2-Al_2O_3的红外光谱研究 被引量:13
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作者 闫鹏 郭海福 +3 位作者 舒华 吴燕妮 刘燕芳 崔秀兰 《化学研究与应用》 CAS CSCD 北大核心 2006年第6期638-642,共5页
以四氯化锡、硫酸铝为原料,氨水为沉淀剂,采用共沉淀法制得新型固体超强酸SO42-/SnO2-A l2O3。采用FT-IR技术考察了金属元素摩尔比、焙烧温度、浸渍液以及掺杂稀土氧化物对该固体超强酸结构和性能的影响。FT-IR结果表明在该固体超强酸中... 以四氯化锡、硫酸铝为原料,氨水为沉淀剂,采用共沉淀法制得新型固体超强酸SO42-/SnO2-A l2O3。采用FT-IR技术考察了金属元素摩尔比、焙烧温度、浸渍液以及掺杂稀土氧化物对该固体超强酸结构和性能的影响。FT-IR结果表明在该固体超强酸中,锡和硫酸根是以螯合和桥式两种方式配位结合,其中起催化活化作用的主要是和硫酸根以螯合双齿结合的锡;和SO42-/ZrO2型超强酸相比,SO42-/SnO2-A l2O3超强酸的硫酸根FT-IR特征吸收峰发生蓝移,显示出更强的酸性。锡铝摩尔比为9∶1、焙烧温度为773K、焙烧时间为3h时,制得的SO42-/SnO2-A l2O3样品对酯化反应的催化性能最好。 展开更多
关键词 ^so4^2-/sno2-Al2O3 固体超强酸 红外光谱
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固体酸SO_4^(2-)/SnO_2催化合成DOP的研究 被引量:9
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作者 陈玉成 陈秀宇 《应用化工》 CAS CSCD 2006年第5期354-356,共3页
采用自制的固体酸SO42-/SnO2为催化剂合成DOP,分别考察了催化剂用量、醇酐比、反应时间等对合成DOP的影响。实验表明,在DOP的合成中最佳的合成条件是:采用14 g的SO42-/SnO2催化剂/mol(苯酐),醇酐比为2.35∶1,反应时间为3.5 h,其酯化率可... 采用自制的固体酸SO42-/SnO2为催化剂合成DOP,分别考察了催化剂用量、醇酐比、反应时间等对合成DOP的影响。实验表明,在DOP的合成中最佳的合成条件是:采用14 g的SO42-/SnO2催化剂/mol(苯酐),醇酐比为2.35∶1,反应时间为3.5 h,其酯化率可达91%以上。SO42-/SnO2作为该反应的催化剂具有催化活性高、寿命长、可多次重复使用、产物易纯化分离、且产品色泽浅等优点,可望代替传统浓硫酸作催化剂应用于DOP的合成。 展开更多
关键词 ^固体酸so4^2-/sno2 邻苯二甲酸二辛酯 催化
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Preparation of SO_4^(2-)/TiO_2-MoO_3 Solid Superacid and Its Catalytic Activity in Acetalation and Ketalation 被引量:7
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作者 杨水金 梁永光 +1 位作者 余协卿 孙聚堂 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2005年第1期51-55,共5页
SO4^2-/TiO2-MoO3, a novel solid superacid, has been prepared and its catalytic activity at different synthetic conditions was examined with esterification of n-butanoic acid and n-butyl alcohol as probing reaction.The... SO4^2-/TiO2-MoO3, a novel solid superacid, has been prepared and its catalytic activity at different synthetic conditions was examined with esterification of n-butanoic acid and n-butyl alcohol as probing reaction.The optimum conditions were also found, that is, the mass ratio of MoO3 used in the compound is 25%, the calcination temperature 450℃, and the soaked consistency of H2SO4 is 0.5mol.L^-1. Then it was applied in the catalytic synthesis of six similar important ketals and acetals as catalyst and revealed high catalytic activity. Under the condition that the molar ratio of aldehyde/ketone to glycol was 1:1.5, the mass ratio of the catalyst to the reactants was 0.5% and the reaction time 1.0 h, the yield of ketals and acetals reached up to 63.2%. The catalyst can be easily recovered and reused. 展开更多
关键词 ^SO_4^(2-)/TiO_2-MoO_3 solid superacid ACETALATION katalation
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Preparation of SO_4^(2-)/TiO_2-La_2O_3 solid superacid and its catalytic activities in acetalation and ketalation 被引量:4
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作者 YANG Shui-jin BAI Ai-min SUN Ju-tang 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2006年第7期553-558,共6页
SO4^2- / TiO2-La2O3, a novel solid superacid, was prepared and its catalytic activities at different synthetic conditions are discussed with esterification of n-butanoic acid and n-butyl alcohol as probing reaction. T... SO4^2- / TiO2-La2O3, a novel solid superacid, was prepared and its catalytic activities at different synthetic conditions are discussed with esterification of n-butanoic acid and n-butyl alcohol as probing reaction. The optimum conditions have also been found, mole ratio of n(La^3+):n(Ti^4+) is 1:34, the soaked consistency of H2SO4 is 0.8 tool/L, the soaked time of HESO4 is 24 h, the calcining temperature is 480 ℃, the calcining time is 3 h. Then it was applied in the catalytic synthesis often important ketals and acetals as catalyst and revealed high catalytic activity. Under these conditions on which the molar ratio of aldehyde/ketone to glycol is l: 1.5, the mass ratio of the catalyst used in the reactants is 0.5%, and the reaction time is 1.0 h, the yields of ketals and acetals can reach 41.4%-95.8%. 展开更多
关键词 ^so4^2-/ TiO2-La2O3 Rare earth solid superacid CATALYSIS
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纳米SO_4^(2-)/SnO_2固体超强酸催化合成环己酮1,2-丙二醇缩酮 被引量:4
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作者 余济伟 高文艺 任立国 《工业催化》 CAS 2006年第10期44-48,共5页
报道了以SnCl4.5H2O为原料和十六烷基三甲基溴化铵为模板剂,采用模板法合成纳米SO42-/SnO2固体超强酸催化剂。用XRD和TG-DTA进行了表征,以环己酮和1,2-丙二醇的缩合反应为探针反应,探讨了SO42-/SnO2固体超强酸的催化活性,较系统地研究... 报道了以SnCl4.5H2O为原料和十六烷基三甲基溴化铵为模板剂,采用模板法合成纳米SO42-/SnO2固体超强酸催化剂。用XRD和TG-DTA进行了表征,以环己酮和1,2-丙二醇的缩合反应为探针反应,探讨了SO42-/SnO2固体超强酸的催化活性,较系统地研究了焙烧温度、反应时间、酮醇物质的量比、带水剂的用量和催化剂的用量等对反应的影响以及催化剂的稳定性。结果表明,SO42-/SnO2固体超强酸催化剂具有纳米大小,在环己酮1,2-丙二醇缩酮的合成具有良好的催化活性和稳定性。在最佳条件下,缩酮的产率可达97.2%,纯度(质量分数)为99.2%。 展开更多
关键词 纳米固体超强酸 ^so4^2-/sno2 环己酮1 2-丙二醇缩酮 催化缩合
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An efficient synthesis of 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one catalyzed by recyclable solid superacid SO_4^(2-)/TiO_2 under grinding condition 被引量:2
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作者 Guo Liang Feng 《Chinese Chemical Letters》 SCIE CAS CSCD 2010年第9期1057-1061,共5页
An efficient synthesis of symmetrical 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one is achieved via a reaction of acenaphthe-nequinone and indoles catalyzed by solid superacid SO4^2-/TiO2 under solvent-free conditions... An efficient synthesis of symmetrical 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one is achieved via a reaction of acenaphthe-nequinone and indoles catalyzed by solid superacid SO4^2-/TiO2 under solvent-free conditions at room temperature by grinding, which provides an efficient route to the synthesis of symmetrical 2,2-bis(1H-indol-3-yl)-2H-acenaphthen-1-one.This procedure offers several advantages including solvent-free conditions,excellent yields of products,simple work-up as well as reuse of catalysts which makes it a useful and attractive protocol for the synthesis of these compounds. 展开更多
关键词 ACENAPHTHENEQUINONE Indole solid superacid ^so4^2-/TiO2 2 2-Bis(1H-indol-3-yl)-2H-acenaphthen-1-one
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固体超强酸SO^(2-)_4/SnO_2催化合成顺丁烯二酸二异辛酯 被引量:3
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作者 毛立新 许怡学 廖德仲 《湖南理工学院学报(自然科学版)》 CAS 2006年第2期59-61,共3页
以顺丁烯二酸酐和异辛醇为原料,用一种高活性的固体超强酸S O24-/SnO 2催化剂催化合成了顺丁烯二酸二异辛酯,研究了酯化反应的优化条件。当n(异辛醇):n(顺丁烯二酸酐)为2.8:1;催化剂用量为酐质量的1.0%时,反应时间120 min,反应温度145℃... 以顺丁烯二酸酐和异辛醇为原料,用一种高活性的固体超强酸S O24-/SnO 2催化剂催化合成了顺丁烯二酸二异辛酯,研究了酯化反应的优化条件。当n(异辛醇):n(顺丁烯二酸酐)为2.8:1;催化剂用量为酐质量的1.0%时,反应时间120 min,反应温度145℃,顺丁烯二酸二异辛酯的收率达到98.7%。同时对用H2SO4和对甲苯磺酸催化该反应作了比较。 展开更多
关键词 顺丁烯二酸二异辛酯 ^so4^2-/sno2 催化合成 固体超强酸
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固体酸SO_4^(2–)/SnO_2催化合成邻苯二甲酸二异辛酯(DIOP) 被引量:1
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作者 陈玉成 吴灵琳 林克平 《漳州师范学院学报(自然科学版)》 2005年第3期94-97,共4页
本文采用了在实验室中制备的固体酸SO42–/SnO2为催化剂合成DIOP,分别考察催化剂用量、醇酐比、反应时间等对合成DOIP产率的影响.实验表明,在DIOP的合成中其最佳工艺操作条件是:采用14g/mol(苯酐)SO42-/SnO2催化剂、醇酐比为2.40:1、反... 本文采用了在实验室中制备的固体酸SO42–/SnO2为催化剂合成DIOP,分别考察催化剂用量、醇酐比、反应时间等对合成DOIP产率的影响.实验表明,在DIOP的合成中其最佳工艺操作条件是:采用14g/mol(苯酐)SO42-/SnO2催化剂、醇酐比为2.40:1、反应时间为4h,其酯化产率可达94%以上.SO42-/SnO2作为该反应的催化剂具有催化活性高、寿命长、可多次重复使用、产物易纯化分离、且产品色泽浅等优点,可望代替传统浓硫酸作催化剂应用于DIOP的合成. 展开更多
关键词 ^固体酸so4^2-/sno2 催化 邻苯二甲酸二异辛酯(DIOP) 合成
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纳米固体超强酸SO_2^(-4)/SnO_2-La_2O_3-SiO_2制备及催化反应研究 被引量:3
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作者 张密林 丁立国 刘文彬 《化工科技》 CAS 2004年第1期44-46,共3页
制备纳米SO2-4/SnO2 La2O3 SiO2固体超强酸催化剂,讨论了在纳米载体SiO2的存在下,Sn、Si摩尔比、焙烧温度对乙酸转化率的影响,并与SO2-4/SnO2 SiO2催化剂进行了对比,讨论了金属La3+对固体超强酸的影响。实验表明,SO2-4/SnO2 La2O3 SiO2... 制备纳米SO2-4/SnO2 La2O3 SiO2固体超强酸催化剂,讨论了在纳米载体SiO2的存在下,Sn、Si摩尔比、焙烧温度对乙酸转化率的影响,并与SO2-4/SnO2 SiO2催化剂进行了对比,讨论了金属La3+对固体超强酸的影响。实验表明,SO2-4/SnO2 La2O3 SiO2催化剂在焙烧温度为450℃,n(Sn)∶n(Si)=0.5时,乙酸的转化率达到98.1%。 展开更多
关键词 固体超强酸催化剂 酯化反应 催化剂 纳米SIO2 催化反应 ^so4^2-/sno2-La2O3-SiO2 焙烧温度 摩尔比
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SO4^2-/SnO2-蒙脱土催化玉米芯水解液制备糠醛 被引量:1
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作者 郭琪 王鹏博 +2 位作者 黄美子 高晓航 卿青 《化工科技》 CAS 2020年第3期38-44,共7页
以蒙脱土(MMT)为载体,采用共沉淀法和浸润法负载金属卤化物和无机酸制备一种新型固体酸催化剂SO 2-4/SnO 2-MMT,其含有双酸位点可以高效催化木糖溶液制备糠醛。在单一水相催化体系中使用该新型固体酸催化剂,190℃反应5 min,从玉米芯水... 以蒙脱土(MMT)为载体,采用共沉淀法和浸润法负载金属卤化物和无机酸制备一种新型固体酸催化剂SO 2-4/SnO 2-MMT,其含有双酸位点可以高效催化木糖溶液制备糠醛。在单一水相催化体系中使用该新型固体酸催化剂,190℃反应5 min,从玉米芯水解产物中催化得到的糠醛产率最高为56.2%,木糖转化率为95.3%。相比于新鲜的蒙脱土,该固体酸催化剂具有合适的路易斯酸位点、布朗斯特酸位点和更大的比表面积、孔体积,促进了木糖的异构化和脱水反应。此外,该催化剂在循环3次后也表现出较好的的催化性能和较高的稳定性。 展开更多
关键词 玉米芯 两步法 ^so4^2-/sno2-蒙脱土 糠醛 可回收性 双酸位点
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同体酸SO4^2-/SnO2催化合成DOP的研究
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作者 陈玉成 陈秀宇 《聚合物与助剂》 2006年第5期43-43,共1页
采用自制的固体酸SO4^2-/SnO2为催化剂合成DOP,分别考察了催化剂用量、醇酐比、反应时间等对合成DOP的影响。实验表明,在DOP的合成中最佳的合成条件是:采用14g的SO4^2-/SnO2催化剂/mpl(苯酐),醇酐比为2.35:1,反应时间为3.5... 采用自制的固体酸SO4^2-/SnO2为催化剂合成DOP,分别考察了催化剂用量、醇酐比、反应时间等对合成DOP的影响。实验表明,在DOP的合成中最佳的合成条件是:采用14g的SO4^2-/SnO2催化剂/mpl(苯酐),醇酐比为2.35:1,反应时间为3.5h,其酯化率可达91%以上。SO4^2-/SnO2作为该反应的催化剂具有催化活性高、寿命长、可多次重复使用、产物易纯化分离、且产品色泽浅等优点,可望代替传统浓硫酸作催化剂用于DOP的合成。 展开更多
关键词 ^so4^2- 催化合成 sno2 DOP 催化剂用量 反应时间 合成条件 催化活性
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The Influence of Aziridine on the Aging of Composite Solid Rocket Propellant
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作者 AMGED A. Ali 《Computer Aided Drafting,Design and Manufacturing》 2008年第1期88-93,共6页
Aging of a solid composite propellant containing HTPB/AP/AL was performed in order to validate the conformance of the accelerated aging data to the Arrhenius law. The main objective of the work was to examine the infl... Aging of a solid composite propellant containing HTPB/AP/AL was performed in order to validate the conformance of the accelerated aging data to the Arrhenius law. The main objective of the work was to examine the influence of the aziridine bonding agents family on the propellant aging. Aging of the prepared propellant samples was conducted as follows: 1. Four samples, one free of bonding agents, and three containing aziridine based bonding agents MAPO,HX-752, MAT4 were aged at 65°C. 2. Another four samples based on HX-752, MAT4 with different curing agents were aged at 65°C. The measured mechanical properties of the free bonding agent propellant samples were very far from the specifications and this illustrates the importance of the bonding agents in both the preparation and the aging phases.The prepared bonding agent 'MAT4' gave remarkable improvements of the mechanical properties comparing with HX-752 and MAPO. The aziridine bonding agents family inhibited the rate of decomposition of the propellant during the aging periods and supported the propellant matrix against decomposition at the elevate temperatures. Using of HMDI as curing agent gave slight better mechanical properties to the IPDI. 展开更多
关键词 AGING solid propellant bonding agents curing agents hydroxy terminated poly butadiene (HTPB) l l(Phenyl Dicarbonyl) bis (2- Methyl Aziridine) (HX-752) Tries[l-(2-methyl) aziridinyl] phosphine oxide (MAPO) reaction product of 2.0 mole of MAPO 0.7mole of adipic acid 0.3 mole of tartaric acid (MAT4) hexamethylene diisocyanate. (HMDI) isophoron diisocyanate (IPDI)
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On the monolayer dispersion behavior of Co_(3)O_(4)on HZSM-5 support:designing applicable catalysts for selective catalytic reduction of nitrogen oxides by ammonia
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作者 Yufeng Yang Lihong Zhang +7 位作者 Tao Song Yixing Huang Xianglan Xu Junwei Xu Xiuzhong Fang Qing Wang Haiming Liu Xiang Wang 《Frontiers of Chemical Science and Engineering》 SCIE EI CSCD 2023年第11期1741-1754,共14页
Based on monolayer dispersion theory,Co_(3)O_(4)/ZSM-5 catalysts with different loadings have been prepared for selective catalytic reduction of nitrogen oxides by ammonia.Co_(3)O_(4)can spontaneously disperse on HZSM... Based on monolayer dispersion theory,Co_(3)O_(4)/ZSM-5 catalysts with different loadings have been prepared for selective catalytic reduction of nitrogen oxides by ammonia.Co_(3)O_(4)can spontaneously disperse on HZSM-5 support with a monolayer dispersion threshold of 0.061 mmol 100 m^(-2),equaling to a weight percentage around 4.5%.It has been revealed that the quantities of surface active oxygen(O_(2)^(-))and acid sites are crucial for the reaction,which can adsorb and activate NO_(x)and NH_(3)reactants effectively.Below the monolayer dispersion threshold,Co_(3)O_(4)is finely dispersed as sub-monolayers or monolayers and in an amorphous state,which is favorable to generate the two kinds of active sites,hence promoting the performance of ammonia selective catalytic reduction of nitrogen oxide.However,the formation of crystalline Co_(3)O_(4)above the capacity is harmful to the reaction performance.4%Co_(3)O_(4)/ZSM-5,the catalyst close to the monolayer dispersion capacity,possesses the most abundant active O_(2)^(-)species and acidic sites,thereby demonstrating the best reaction performance in all the samples.It is proposed the optimal Co_(3)O_(4)/ZSM-5 catalyst can be prepared by loading the capacity amount of Co_(3)O_(4)onto HZSM-5 support. 展开更多
关键词 Co_(3)O_(4)/ZSM-5 NO_(x)-SCR by NH_(3) monolayer dispersion threshold effect surface acid sites surface active ^O_(2)^(-)anions
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醇、酚、胺的酰化催化剂
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作者 李春刚(摘) 王国平(校) 《中国医药工业杂志》 CAS CSCD 北大核心 2009年第3期167-167,共1页
醇、酚、胺以0.5m01%SO4^2-/SnO2为催化剂(有文献),不加溶剂与乙酸酐室温搅拌10-60min,得乙酰化物,17例收率88%~95%。羟基与氨基同时存在可选择性乙酰化氨基,4例收率88%~99%。另5例用其它酸酐,酰化物收率90%~95%。
关键词 酰化催化剂 ^so4^2- 乙酰化物 sno2 可选择性
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Investigation and Application of Polarographic Catalytic Wave of Oxygen Reduction Caused by Mefenamic Acid 被引量:1
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作者 宋俊峰 过玮 +1 位作者 亢晓峰 胡荫华 《Science China Chemistry》 SCIE EI CAS 1993年第8期906-911,共6页
The polarographic catalytic wave of oxygen reduction caused by mefenamic acid (MA) with redox properties was reported in this paper. The electrochemical process of the catalytic wave was proposed that the superoxide a... The polarographic catalytic wave of oxygen reduction caused by mefenamic acid (MA) with redox properties was reported in this paper. The electrochemical process of the catalytic wave was proposed that the superoxide anion O(?) was generated polarographically and the dismutation of the O(?) was catalyzed by MA to reproduce O_2 and H_2O_2. This explained chemically the scavenging of the O_2^- by MA im biomedical area. Based on the catalytic wave, a new method for the determination of MA by single-sweep polarography was developed. 展开更多
关键词 mefenamic acid[61-68-7] pharmaceutical chemistry superoxide anion ^O_2^+[11062-77-4] DISMUTATION polarographic catalytic wave.
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