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Steam reforming of acetic acid over Ni-Ba/Al2O3 catalysts:Impacts of barium addition on coking behaviors and formation of reaction intermediates 被引量:2
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作者 Zhanming Zhang Yiran Wang +7 位作者 Kai Sun Yuewen Shao Lijun Zhang Shu Zhang Xiao Zhang Qing Liu Zhenhua Chen Xun Hu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2020年第4期208-219,共12页
The influence of barium addition to a Ni/Al2O3 catalyst on the reaction intermediates formed,the activity,resistance of the catalyst to coking,and properties of the coke formed after acetic acid steam reforming were i... The influence of barium addition to a Ni/Al2O3 catalyst on the reaction intermediates formed,the activity,resistance of the catalyst to coking,and properties of the coke formed after acetic acid steam reforming were investigated in this study.The results showed the drastic effects of barium addition on the physicochemical properties and performances of the catalyst.The solid-phase reaction between alumina and BaO formed BaAl2O4,which re-constructed the alumina structure,resulting in a decrease in the specific surface area and an increase in the resistance of metallic Ni to sintering.The addition of barium was also beneficial for enhancing the catalytic activity,resulting from the changed catalytic reaction network.The in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) study of the acetic acid steam reforming indicated that barium could effectively suppress the accumulation of the reaction intermediates of carbonyl,formate,and C=C functional groups on the catalyst surface,attributed to its relatively high ability to cause the gasification of these species.In addition,coking was considerably more significant over the Ba-Ni/Al2O3 catalyst.Moreover,the Ba-Ni/Al2O3 catalyst was more stable than the Ni/Al2O3catalyst,owing to the distinct forms of coke formed (carbon nanotube form over the Ba-Ni/Al2O3 catalyst,and the amorphous form over the Ni/Al2O3 catalyst). 展开更多
关键词 BARIUM ADDITION Nickel-based CATALYSTS Steam reforming of acetic acid reaction INTERMEDIATES COKING BEHAVIORS
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Improved two-step hydrothermal process for acetic acid production from carbohydrate biomass 被引量:1
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作者 Zhibao Huo Yan Fang +3 位作者 Guodong Yao Xu Zeng Dezhang Ren Fangming Jin 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2015年第2期207-212,共6页
An improved two-step process for converting carbohydrate biomass to acetic acid under hydrothermal conditions is proposed. The first step consists of the production of lactic acid from carbohydrate biomass, and the se... An improved two-step process for converting carbohydrate biomass to acetic acid under hydrothermal conditions is proposed. The first step consists of the production of lactic acid from carbohydrate biomass, and the second step consists of conversion of the lactic acid obtained in the first step to acetic acid using CuO as an oxidant. The results indicated that CuO as an oxidant in the second step can significantly improve the production of high-purity acetic acid from lactic acid, and the maximum yield of acetic acid was 61%, with a purity of 90%. The yield of acetic acid obtained using the improved two-step hydrothermal process from carbohydrate biomass, such as glucose, cellulose and starch, was greater than that obtained using traditional two-step process with H2O2 orO2. In addition, a proposed pathway for the production of acetic acid from lactic acid in the second step with CuO was also discussed. The present study provides a useful two-step process for the production of acetic acid from carbohydrate biomass. 展开更多
关键词 碳水化合物 生物量 乙酸 生产 水热方法 最大产率 水热条件 氧化剂
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Theoretical Study on the Reaction Mechanism of o-Aminophenol, Acetic Acid and Phosphorus Oxytrichloride One-pot to Form 2-Methyl Benzoxazole
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作者 张福兰 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2018年第12期1869-1877,1843,共10页
The reaction mechanism of o-aminophenol, acetic acid and phosphorus oxytrichloride in one-pot to form 2-methyl benzoxazole was studied by density functional theory. The geometries of the reactants, transition states, ... The reaction mechanism of o-aminophenol, acetic acid and phosphorus oxytrichloride in one-pot to form 2-methyl benzoxazole was studied by density functional theory. The geometries of the reactants, transition states, intermediates and products were optimized at the GGA/PW91/DNP level. Vibration analysis was carried out to confirm the transition state structure. Two possible reaction pathways were investigated in this study. The result indicates that the reaction Re→TS1→IM1→TSA2→IMA2→TSA3→IMA3→TSA4→IMA4→TSA5→P2 is the main pathway, the activation energy of which is the lowest. Re→TS1→IM1 is the rate-limiting step, with the activation energy being 221.54 kJ·mol^(-1) and the reaction heat being 10.06 kJ·mol^(-1). The dominant product predicted theoretically is in agreement with the experiment results. 展开更多
关键词 O-AMINOPHENOL acetic acid PHOSPHORUS oxytrichloride 2-methyl BENZOXAZOLE density functional reaction mechanism
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Recovery of Dilute Acetic Acid by Catalytic Distillation Using NKC-9 as Catalyst 被引量:1
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作者 张志刚 李晓峰 +1 位作者 徐世民 李鑫钢 《Transactions of Tianjin University》 EI CAS 2006年第4期264-270,共7页
反应动力学冲淡有把 NKC-9 用作催化剂的甲醇的乙酸在 308 K 的温度被学习, 318 K, 323 K, 328 K。运动模型基于 onLangmuir-Hinshei-wood 率模型被导出,活化能是 6.13 X 10 ~ 4 kJ/kmol。恢复的 Theexperiment 冲淡乙酸在一张填充... 反应动力学冲淡有把 NKC-9 用作催化剂的甲醇的乙酸在 308 K 的温度被学习, 318 K, 323 K, 328 K。运动模型基于 onLangmuir-Hinshei-wood 率模型被导出,活化能是 6.13 X 10 ~ 4 kJ/kmol。恢复的 Theexperiment 冲淡乙酸在一张填充床被进行催化蒸馏柱。决定做到乙酸的 85.9percent 变换的最佳的进程参数和运作的条件如下;催化剂床的高度是 1 100 公里,回流比是 4:1,并且到乙酸的甲醇的比率是 2:1。方法能在 15%-30 百分比的工业规模恢复被用作一个指南冲淡乙酸。 展开更多
关键词 蒸馏 乙酸 催化剂 反应动力学 NKC-9
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Studies on Solid State Reactions of Coordination Compounds(LXXI)──Solid State Reactions of o-Aminobenzoic Acid with Copper(Ⅱ) Acetate and Formate at Room Temperature
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作者 ZHENG Li-min LIN Jian-jun FU Yan and XIN Xin-quan (Department of Chemistry , Manjing University , Naiijing , 210008) 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 1995年第1期45-49,共5页
StudiesonSolidStateReactionsofCoordinationCompounds(LXXI)──SolidStateReactionsofo-AminobenzoicAcidwithCopper... StudiesonSolidStateReactionsofCoordinationCompounds(LXXI)──SolidStateReactionsofo-AminobenzoicAcidwithCopper(Ⅱ)AcetateandForm... 展开更多
关键词 SOLID STATE reaction o-Aminobenzoic acid COPPER ACETATE COPPER FORMATE Electrical conductivity
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Synthesis of Coordination Polymers Using Different Maleic Acid Ligands under Hydrothermal Conditions
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作者 WANG Xiao-lan WANG En-bo XU Xin-xin 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2007年第3期245-249,共5页
A novel coordination polymer, [Ni(mal)(1,10′-phen)(H2O)]n(1)(mal=malate, 1,10′-phen=1,10-phenanthroline) was synthesized using malic acid which was generated from maleic acid via hydrothermal reaction. Complex 1, wh... A novel coordination polymer, [Ni(mal)(1,10′-phen)(H2O)]n(1)(mal=malate, 1,10′-phen=1,10-phenanthroline) was synthesized using malic acid which was generated from maleic acid via hydrothermal reaction. Complex 1, which displays a two-dimensional supramolecular network, was formed by the addition reaction of Ni and maleic acid with water molecules. To our knowledge, several coordination polymers have been directly synthesized from malic acid, but these types of complexes have seldom been synthesized from maleic acid via hydrothermal reactions. When Ni(Ⅱ) ion was changed to Zn(Ⅱ) ion under the same condition, two-dimensional covalent complex 2[Zn2(fma)2(1,10′-phen)2]n(fma=fumatic acid) was formed. Furthermore, complex 2 exhibits intense photoluminescent property at room temperature. 展开更多
关键词 马来酸配位体 配位聚合物 合成 水热条件 光致发光
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重组木聚糖酶的高密度发酵及其定向制备低聚木糖
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作者 赵剑 解静聪 +3 位作者 姜越 杨静 徐浩 张宁 《林产化学与工业》 CAS CSCD 北大核心 2024年第1期97-104,共8页
为提高酶水解杨木木聚糖定向转化低聚木糖的效率,同时降低酶法制备低聚木糖的成本,围绕重组大肠杆菌(PET-PdoXyn10A-DE3)高密度发酵制备拟杆菌来源木聚糖酶PdoXyn10A的诱导表达条件和酶水解制备低聚木糖的工艺条件开展了研究。考察了在... 为提高酶水解杨木木聚糖定向转化低聚木糖的效率,同时降低酶法制备低聚木糖的成本,围绕重组大肠杆菌(PET-PdoXyn10A-DE3)高密度发酵制备拟杆菌来源木聚糖酶PdoXyn10A的诱导表达条件和酶水解制备低聚木糖的工艺条件开展了研究。考察了在5 L发酵罐水平下诱导剂浓度、诱导光密度(OD_(600))值、诱导温度和诱导pH值等因素对PET-PdoXyn10A-DE3产重组木聚糖酶PdoXyn10A的影响,反应温度、pH值对玉米芯木聚糖酶水解过程中酶活力的影响,以及酶添加量、酶水解时间对杨木乙酸水解液制备低聚木糖的影响。研究结果表明:在诱导剂浓度0.25 mmol/L、诱导OD_(600)值55、诱导温度34℃和诱导pH值7.0的最佳诱导条件下,经高密度发酵重组酶酶活力可达362.67 U/mL,重组大肠杆菌生物量可达28.83 g/L。酶水解制备低聚木糖的最佳条件为酶反应温度40℃、pH值5.2、酶添加量12 U/mL和反应时间6 h,此条件下低聚木糖的量为3.21 g/L,其中木二糖、木三糖、木四糖、木五糖和木六糖的量分别为1.09、 0.97、 0.84、 0.18、 0.13 g/L,木糖为1.82 g/L。 展开更多
关键词 重组木聚糖酶 高密度发酵 乙酸水热反应 低聚木糖 酶水解条件
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CH_(4)和CO_(2)共转化反应机理研究进展
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作者 成昊霖 年瑶 韩优 《化工进展》 EI CAS CSCD 北大核心 2024年第1期60-75,共16页
综述了CH_(4)和CO_(2)共转化生成合成气、乙酸和C2烃3种反应路径的反应步骤、关键中间体及反应产物选择性的影响因素。当生成合成气时,CH_(4)与CO_(2)的活化解离是关键步骤,催化剂载体表面为酸性或中性时反应遵循单功能机理,CH_(4)和CO_... 综述了CH_(4)和CO_(2)共转化生成合成气、乙酸和C2烃3种反应路径的反应步骤、关键中间体及反应产物选择性的影响因素。当生成合成气时,CH_(4)与CO_(2)的活化解离是关键步骤,催化剂载体表面为酸性或中性时反应遵循单功能机理,CH_(4)和CO_(2)在同一活性中心被活化,当载体为表面碱性时,CH_(4)和CO_(2)遵循双功能机理,在不同活性中心被活化,通常双功能机理的催化效率更高。当生成乙酸时,C-C耦合过程应被重点关注,该过程中气相CO_(2)可能直接插入M—CH3键(Eley-Rideal机理)或先被吸附活化后再插入(Langmuir-Hinshelwood机理),后者反应能垒更低。当生成C2烃时,活性氧物种被认为是反应过程中的关键中间体,其可能来源于催化剂中的晶格氧或CO_(2)的活化与解离。因此,在催化剂表面构建多个独立活性位点,以分别对CH_(4)和CO_(2)进行多位点协同催化被认为是良好的催化剂改性策略。另外,先进的模拟计算方法和原位表征手段能够深入揭示反应过程中催化剂和反应中间体的动态演变过程及机理,从而为真实CH_(4)和CO_(2)共转化反应过程中催化剂的设计提供理论指导。 展开更多
关键词 甲烷 二氧化碳 反应机理 合成气 乙酸 C2烃
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乙酸正丙酯制备条件的优化研究
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作者 常越凡 和婧 《山西化工》 CAS 2024年第2期9-11,共3页
以乙酸和正丙醇为原料,以浓硫酸为催化剂合成乙酸正丙酯。通过优化催化剂用量、反应温度以及酯化反应时间3个条件,得到了纯度和产率较高的乙酸正丙酯。实验结果表明,当加入催化剂体积为1.5 mL,在100℃下反应时间为50 min时,乙酸正丙酯... 以乙酸和正丙醇为原料,以浓硫酸为催化剂合成乙酸正丙酯。通过优化催化剂用量、反应温度以及酯化反应时间3个条件,得到了纯度和产率较高的乙酸正丙酯。实验结果表明,当加入催化剂体积为1.5 mL,在100℃下反应时间为50 min时,乙酸正丙酯的精制收率可达到87.8%。 展开更多
关键词 乙酸正丙酯 浓硫酸 反应温度 酯化时间
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外源氨基酸对废弃烟草水热液相香味产物的影响
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作者 岳先领 刘克强 +5 位作者 关体青 聂红资 朱鑫超 梁淼 张峻松 姜涛 《农产品加工》 2024年第2期21-26,共6页
以废弃烟草为原料,在外加氨基酸的条件下通过水热反应技术将其转化为水热液相香味物质,考查了反应温度和氨基酸种类对液相产物种类和成分的影响。结果表明,不同反应温度和氨基酸引入的条件下,烟草水热液相产物中共检测出81种挥发性香味... 以废弃烟草为原料,在外加氨基酸的条件下通过水热反应技术将其转化为水热液相香味物质,考查了反应温度和氨基酸种类对液相产物种类和成分的影响。结果表明,不同反应温度和氨基酸引入的条件下,烟草水热液相产物中共检测出81种挥发性香味成分。升高温度可明显提升甲基环戊烯醇酮(MCP)、乙基环戊烯醇酮(ECP)、麦芽醇、苯酚、愈创木酚,烟碱等物质含量。通过参与美拉德反应,外加脯氨酸与丙氨酸可促进香味物质产生,前者促进酮类香味物质产生,后者则有利于吡嗪类香味物质的产生。感官评价表明,特定反应条件下的烟草水热液相香味物质具有提升卷烟抽吸品质的作用。 展开更多
关键词 低次烟叶 氨基酸 水热液化反应
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Microporous Silica-supported Polyoxometalate Catalyst H_3PW_(12)O_(40)/SiO_2 with High Activity for Acetal Reaction between Benzaldehyde and Ethylene Glycol 被引量:1
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作者 YANG Yu lin 1,2 , WANG Yong hui 1, HU Chang wen 1,** , WANG En bo 1 and FENG Shou hua 2 (1. Institute of Polyoxometalate Chemistry, Faculty of Chemistry, Northeast Normal University, Changchun 130024, P. R. China 2. State Key Laboratory 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2002年第2期223-225,共3页
关键词 SILICA-SUPPORTED 12-tungstophosphoric acid Catalysis ACETAL reaction
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Photo-degradation of Acid-red 3B dye catalyzed by TiO_2 nanotubes 被引量:6
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作者 JIANG Fang ZHENG Shou-rong ZHENG Zheng XU Zhao-yi WANG Yan-jin 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2006年第4期783-787,共5页
TiO2 nanotube precursor was synthesized by the hydrothermal reaction o f TiO2 powders with NaOH solution and the properties of the nanotube materials w ere tuned using different post-treatments. Transmission electron ... TiO2 nanotube precursor was synthesized by the hydrothermal reaction o f TiO2 powders with NaOH solution and the properties of the nanotube materials w ere tuned using different post-treatments. Transmission electron microscopic (TE M) observation revealed that the nanotube could be obtained by either a direct r inse with acid solution or rinse with distilled water followed by acid solution. The results of X-ray diffraction (XRD) and inductively coupled plasma (ICP) ana lysis indicated that the nanotube material was composed of H2Ti2O5·H2O. In addi tion, the photocatalytic activities of the resulting catalysts were found to be strongly dependent on the post-treatment. The results of the photocatalytic reac tion showed that the degradation of Acid-red 3B dye fitted pseudo-zero-order kin etics and TiO2 nanotube prepared under direct rinse with acid solution exhibited a higher catalytic efficiency compared to other catalysts. 展开更多
关键词 二氧化钛 纳米管 光催化作用 热液反应 染料 废水处理
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Hydrothermal Synthesis, Crystal Structure and Photoluminescence of [Sm(PCA)_3(H_2O)_2]_n·6nH_2O 被引量:1
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作者 陈文通 魏坤宇 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2011年第5期672-677,共6页
A new one-dimensional (1-D) compound [Sm(PCA)3(H2O)2]n·6nH2O (1, HPCA=pyrazinecarboxylic acid) has been synthesized via hydrothermal reaction and structurally characterized by single-crystal X-ray diffraction. Co... A new one-dimensional (1-D) compound [Sm(PCA)3(H2O)2]n·6nH2O (1, HPCA=pyrazinecarboxylic acid) has been synthesized via hydrothermal reaction and structurally characterized by single-crystal X-ray diffraction. Compound 1 crystallizes in the Pbca space group of orthorhombic system with a=19.465(3), b=12.034(4), c=19.842(4) , V=4648(2)3, C15H25N6O14Sm, Mr=663.76, Dc=1.897 g/cm3, S=1.023, μ(MoKα)=2.610 mm-1, F(000)=2648, R=0.0239 and wR=0.0616. Compound 1 is characteristic of an infinite 1-D chain-like structure with the samarium atoms locating at an environment of a monocapped square antiprism. The [Sm(PCA)3(H2O)2]n chains and the lattice water molecules interconnect together through π-π interactions and hydrogen bonding interactions to yield a 3-D supramolecular framework. Photoluminescent investigation reveals that the title compound displays an emission in the greenish blue region. 展开更多
关键词 水热合成 光致发光 晶体结构 氢键相互作用 标题化合物 HPCA 反应合成 正交晶系
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Copper-mediated synthesis of N,N'-diarylhydrazines from boronic acids
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作者 Ye Feng Wang Yuan Zhou Jia Rui Wang Lei Liu Qing Xiang Guo 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第5期499-501,共3页
N,N0-Diarylhydrazines have been prepared via the reaction of N-Boc-aryl hydrazines with boronic acids mediated by copper acetate. This mild reaction condition tolerates the presence of a variety of functional groups.
关键词 N N′-二芳基肼类化合物 合成 硼酸 交叉偶联反应 醋酸铜
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Hydrothermal Assembly and Structural Characterization of a Novel 3D Coordination Polymer: [Cd_2Zn(BTC)_2(H_2O)_4]_n·2nH_2O
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作者 陈建新 刘世雄 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2005年第1期3-3,共1页
A hydrothermal reaction of 1,3,5-benzene-tricarboxylic acid (H3BTC) with cad- mium acetate, zinc acetate and pyridine led to the formation of pink crystals of [Cd2Zn(BTC)2- (H2O)4]n?2nH2O 1. Single-crystal X-ray diffr... A hydrothermal reaction of 1,3,5-benzene-tricarboxylic acid (H3BTC) with cad- mium acetate, zinc acetate and pyridine led to the formation of pink crystals of [Cd2Zn(BTC)2- (H2O)4]n?2nH2O 1. Single-crystal X-ray diffraction analysis has revealed that 1 (Cd2ZnC18H18O18) crystallizes in the monoclinic system, space group C2/c with a = 19.4328(7), b = 7.1420(3), c = 18.0426(5) ?, β = 118.035(1)o, V = 2210.3(1) ?3, Mr = 812.49, Dc = 2.442 g/cm3, Z = 4, μ(MoKα) = 3.081 mm-1 and F(000) =1584. A total of 10735 reflections were collected, of which 2544 were unique. The structure was refined to R = 0.0200 and wR = 0.0603 for 2388 observed reflections with I>2σ(I). The crystal structure consists of cadmium(II)/zinc(II) carboxylates of BTC as well as coordination and discrete water molecules. Extension of the coordination geometry around three metal centers (Cd(1), Cd(2) and Zn(1)), two BTC3- ligands and four coordinated water molecules generates a three-dimensional coordination polymer. 展开更多
关键词 镉配合物 [Cd2Zn(BTC)2(H2O)4]n·2nH2O 水热反应 配位高聚物 1'3'5-苯-三羧酸
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CH_(4)和CO_(2)偶联直接合成乙酸的研究进展 被引量:1
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作者 黄伟 陶诗琪 《低碳化学与化工》 CAS 北大核心 2023年第2期1-13,共13页
CH_(4)和CO_(2)偶联直接合成乙酸是典型的绿色化学反应之一,但是也是一个热力学不利的过程,实现该反应是化学工程与技术的巨大挑战。CH_(4)和CO_(2)作为性质稳定的化合物,在温和条件下的活化与转化是催化领域的难题。综述了近年来国内外... CH_(4)和CO_(2)偶联直接合成乙酸是典型的绿色化学反应之一,但是也是一个热力学不利的过程,实现该反应是化学工程与技术的巨大挑战。CH_(4)和CO_(2)作为性质稳定的化合物,在温和条件下的活化与转化是催化领域的难题。综述了近年来国内外CH_(4)和CO_(2)偶联直接合成乙酸的研究进展,重点介绍了克服热力学不利的方法、反应机理以及催化剂研发等方面的工作,分析了构建高性能催化剂可行的方向,展望了CH_(4)和CO_(2)偶联直接合成乙酸的未来发展方向,并提出了相关建议。 展开更多
关键词 CH_(4)活化 CO_(2)利用 乙酸 催化剂 热力学限制反应
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乙酸基+O_(2)及其分解异构化反应速率常数计算和不确定度分析
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作者 殷阁媛 肖波 +1 位作者 胡二江 黄佐华 《西安交通大学学报》 EI CAS CSCD 北大核心 2023年第5期109-117,共9页
为了构建准确乙酸燃烧化学反应动力学模型,进行了乙酸基与O_(2)及其分解异构化高精度的量子计算。利用CCSD(T)-F12/cc-pVTZ-F12//B2PLYPD3/cc-pVTZ算法,得到了反应体系势能面,并基于多参考态方法CASPT2/CBS//CASPT2/cc-pVTZ,获得无势垒... 为了构建准确乙酸燃烧化学反应动力学模型,进行了乙酸基与O_(2)及其分解异构化高精度的量子计算。利用CCSD(T)-F12/cc-pVTZ-F12//B2PLYPD3/cc-pVTZ算法,得到了反应体系势能面,并基于多参考态方法CASPT2/CBS//CASPT2/cc-pVTZ,获得无势垒反应势能面。通过气相单分子反应理论(RRKM)和主方程理论求解了温度和压力相关的速率常数,利用可变反应坐标过渡态理论求解无势垒反应乙酸基与O_(2)加成反应的速率常数。结果表明:在低压或者高温条件下,超过99%的化学活化的O_(2)CH_(2)CO_(2)H自由基直接分解为CH_(2)O_(2)H+CO_(2)。随着压力升高,化学活化的O_(2)CH_(2)CO_(2)H碰撞稳定后生成O_(2)CH_(2)CO_(2)H,O_(2)CH_(2)CO_(2)H则在后续反应中分解为CH_(2)O_(2)H+CO_(2)。乙酸自由基在分解时,CO_(2)+CH_(3)产物通道占据主导地位。基于计算结果改进了原有乙酸模型,改进后的模型能够更好地预测层流燃烧速度,并且乙酸基存在更多的消耗路径,与量化计算结果一致。 展开更多
关键词 酸雨 乙酸 无势垒反应 主方程理论
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木质素基水热碳负载钌催化乙酰丙酸加氢反应
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作者 张泽晓 袁冰 +1 位作者 解从霞 于世涛 《青岛科技大学学报(自然科学版)》 CAS 2023年第5期52-57,共6页
采用木质素磺酸钠为原料制备水热碳负载钌(Ru/LHC-xA)催化乙酰丙酸加氢反应制备γ-戊内酯,使用拉曼、SEM、XPS等手段对催化剂进行了表征。探讨了木质素磺酸钠基水热碳制备时的水-酸比、反应中催化剂的用量及反应温度、压力和水用量对乙... 采用木质素磺酸钠为原料制备水热碳负载钌(Ru/LHC-xA)催化乙酰丙酸加氢反应制备γ-戊内酯,使用拉曼、SEM、XPS等手段对催化剂进行了表征。探讨了木质素磺酸钠基水热碳制备时的水-酸比、反应中催化剂的用量及反应温度、压力和水用量对乙酰丙酸加氢反应的影响,并对催化剂循环使用性进行了考察。在以水-酸比0.2制备的水热碳为载体,浸渍负载得到的20 mg Ru/LHC-0.2A(钌质量分数5%)催化剂作用下,10 mmol乙酰丙酸于5 mL水中,1.5 MPa初始氢气压力,80℃反应2 h,可获得99.3%的乙酰丙酸转化率和98.9%的γ-戊内酯选择性。回收后循环使用的催化剂在使用5次后选择性保持稳定,转化率有所下降,但仍高于90%。 展开更多
关键词 木质素磺酸钠 水热碳 乙酰丙酸 γ-戊内酯 加氢反应
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硅锰渣基沸石的合成及其表征
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作者 董雄伟 韩凤兰 +3 位作者 华炜 李茂辉 安长聪 黄玉才 《无机盐工业》 CAS CSCD 北大核心 2023年第12期128-132,共5页
硅锰渣是生产硅锰合金时产生的一种工业副产物,年排放量巨大,综合利用水平低,已经成为冶金业绿色发展急需解决的难题。为实现硅锰渣的高值化利用,将硅锰渣通过“酸洗—碱熔—陈化—晶化”水热合成反应来制备沸石。采用X射线衍射仪(XRD)... 硅锰渣是生产硅锰合金时产生的一种工业副产物,年排放量巨大,综合利用水平低,已经成为冶金业绿色发展急需解决的难题。为实现硅锰渣的高值化利用,将硅锰渣通过“酸洗—碱熔—陈化—晶化”水热合成反应来制备沸石。采用X射线衍射仪(XRD)、扫描电子显微镜(SEM)、傅里叶红外光谱仪(FT-IR)、比表面积及孔径分析仪对沸石的晶相、形貌、官能团等进行表征;探究了碱度、温度、时间等因素对合成沸石的物相组成及微观形貌的影响。实验结果表明,原料酸浸后MnO、Fe_(2)O_(3)、CaO含量均有所减少,碱熔后体系中生成了合成沸石所需的硅酸盐。在最优条件(碱度为0.5 mol/L、温度为80℃、时间为8 h)下合成了纯度及结晶度较好的沸石;与传统的工业固废制备沸石相比,该实验晶化所需的碱度更低,且采用了硅锰渣为原料制备沸石,为硅锰渣的高值化利用提供了新思路。 展开更多
关键词 硅锰渣 沸石 水热反应 酸浸 碱熔
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乙酰苯胺合成实验的改进
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作者 杨玉峰 韩春亮 《河南教育学院学报(自然科学版)》 2023年第2期55-58,共4页
实验教材以苯胺为底物、乙酸为酰化试剂,采用分馏法合成乙酰苯胺,分馏温度不易控制、产率低。以自制简易精馏装置、等摩尔量的乙酸和苯胺混合液逐滴滴入沸腾过量乙酸中的加料方式、反应精馏合成乙酰苯胺,实验操作容易、重现性好、反应... 实验教材以苯胺为底物、乙酸为酰化试剂,采用分馏法合成乙酰苯胺,分馏温度不易控制、产率低。以自制简易精馏装置、等摩尔量的乙酸和苯胺混合液逐滴滴入沸腾过量乙酸中的加料方式、反应精馏合成乙酰苯胺,实验操作容易、重现性好、反应时间短、产率高、过程环保。通过对教材中经典实验的改进、延伸与拓展,调动了学生对实验研究的积极性,提高了他们分析问题和解决问题的能力,可在本科生实验中大力推广。 展开更多
关键词 乙酸 苯胺 乙酰苯胺 酰化反应
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