共查询到19条相似文献,搜索用时 62 毫秒
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次氯酸钠在2,2,6,6-四甲基哌啶氧化物(TEMPO)的催化下,可在温和的条件下选择性氧化胆酸类化合物的C3位羟基.该方法提供了与常规的氧化剂相反的区域选择性,为胆酸类化合物的结构改造提供了简洁的路线. 相似文献
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将交联聚苯乙烯(CPS)微球表面固载有2,2,6,6-四甲基哌啶氮氧自由基(TEMPO)的非均相催化剂微球(TEMPO/CPS)与过渡金属盐相结合,构成复合催化剂体系,用于分子氧对肉桂醇的氧化过程的研究。 分别采用高价金属离子氧化性比硝酸根NO 3 - 更弱和更强的两类过渡金属盐为助催化剂,与微球TEMPO/CPS构成组合催化剂,深入探索研究了其催化性能与催化机理。 研究结果表明,几种过渡金属盐(如Fe、Cu、Mn、Co盐)与微球TEMPO/CPS形成的复合催化剂,可有效地催化分子氧对肉桂醇的氧化过程,将其转化为唯一的产物肉桂醛。 以过渡金属硝酸盐为助催化剂,当硝酸盐结构中对应的高价态(氧化态)金属离子的氧化性比NO 3 - 离子弱时(如Fe(NO3)3与Cu(NO3)2),正负离子共同发挥助催化作用;当硝酸盐结构中对应的高价态(氧化态)金属离子的氧化性比NO 3 - 离子强时,比如Co(NO3)2与Mn(NO3)2对应的Co(Ⅲ)与Mn(Ⅲ)离子,金属离子单独发挥助催化作用,NO 3 - 离子不起作用。 实验结果表明,对于肉桂醇的分子氧催化氧化,在几种过渡金属盐中,Fe(NO3)3作为最适宜的助催化剂,温和条件下(55 ℃、常压O2),可高效地将肉桂醇转化为肉桂醛,转化率为92%。 相似文献
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等离子体化学气相沉积(PCVD)法可制备多孔柱状结构的SnO_2超微粒非晶薄膜,本文研究了薄膜在真空吸附体系中的膜电阻和IR谱随温度变化特性及乙二醇、正丙醇、异丙醇、乙醇和甲醇的气敏灵敏度,提出SnO_2薄膜上吸附氧O_2~-、O~-对醇的氧化机理 1实验与结果 自制PCVD装置抽空后充入40 Pa的O_2,加高频出现辉光,再充入CnCl_4使辉光转为蓝 相似文献
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CuI/TPA(tris(pyridin-2-ylmethyl)amine)/4-乙酰胺基-TEMPO(2,2,6,6-Tetramethylpiperidyl-1-oxyl)催化体系能够在室温下,以氧气作氧化剂,乙腈作溶剂,高效、高选择性地催化一系列苄醇,烯丙基醇和含杂原子伯醇的氧化,且在体系中无需添加任何碱作助催化剂. 相似文献
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Interest in conversion of natural gas to liquid hydrocarbons (GTL) by Fischer-Tropsch synthesis has grown significantly over the last decade. Most research and development work has focused on syngas production step, which accounts for more than 50% of the total investment. Reducing the cost of syngas production would have great beneficial effects on GTL process. Catalytic partial oxidation of methane (CPOM) to syngas is a slightly exothermic, highly selective, and energy efficient process. It gives syngas with n(H2)/n(CO)=2, directly suitable for F-T synthesis. However, CPOM process has not yet been used commercially. The major engineering problems are the high temperature gradient and the risk of explosion with premixed CH4-O2 mixture, which is within the ignition and explosion limit. In fluidized-bed reactors, the heat transfer is much better, which ensures a more uniform temperature and safer operation. A technology for syngas production by contacting CH4 with limited amount of steam and O2 in a fluidized-bed reactor has been developed[1]. 相似文献
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Daobo Yu Puyi Lei Yanfang Li Dr. Wenzhuo Shen Dr. Min Zhong Dr. Jiali Zhang Prof. Dr. Shouwu Guo 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(18):e202104380
Chemoselectively oxidizing Cα−OH to C=O has been considered as a key step for the oxidative depolymerization of lignin. In this work, we design and prepare a series of composites of RuCo alloy nanoparticles and reduced graphene oxide (RuCo/rGO) with different Ru to Co ratios and explore their catalytic activities in the oxidation of veratryl alcohol derivatives, which usually serve as the model compounds for studying lignin oxidation. It is illustrated that the Ru to Co ratio determines the morphology and average size of the RuCo alloy nanoparticles on rGO, and the overall catalytic activities of the composites. The RuCo alloy nanoparticles on rGO with Ru to Co ratios of 1 : 0 to 1.2 : 1 show a unique flower-shaped morphology that increases the exposure of the active sites and thus promotes their contact with the substrates. The RuCo/rGO composites exhibit high catalytic activities for the oxidation of Cα−OH to aldehydes at 100 °C for 2 h. Additionally, the Co component affords the RuCo/rGO composites with magnetic properties that make the separation and recovery of the catalyst simple. Given the high catalytic performances and easy recovery, the RuCo/rGO composites would be potentially useful for the depolymerization of lignin. 相似文献
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本文采用浸渍涂覆法成功制备出多孔Ti负载纳米Co3O4电催化膜电极(Co3O4/Ti),以该膜电极为阳极,辅助电极为阴极,构建电催化膜反应器(electrocatalytic membrane reactor,ECMR)用于可控催化氧化苯甲醇制备苯甲醛和苯甲酸,并考察了 Co3O4/Ti 膜电极结构、电化学性能以及ECMR不同操作参数对苯甲醇转化率、苯甲醛和苯甲酸选择性的影响. 结果表明,负载Co3O4纳米颗粒可以显著提高Ti膜电极的电化学性能和催化活性. 在常温常压下,当反应物苯甲醇浓度为10 mmol·L-1,pH为7.0,停留时间为5.0 min,电流密度为2.5 mA·cm-2,苯甲醇的转化率达到49.8%,苯甲醛选择性为51.5%,苯甲酸选择性为23.6%. 相似文献
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以硝酸铜和均苯三甲酸(BTC)为原料,水热合成了一种金属有机骨架化合物Cu-BTC,在水相中催化苯甲醇选择氧化反应,H2O2氧化剂,优化了Cu-BTC的晶化条件.70℃反应1 h,Cu-BTC(110C/24 h)上的苯甲醇转化率为75.4%、苯甲醛选择性83.5%,但反应后Cu-BTC骨架完全塌陷.在氮气中高温焙烧Cu-BTC,制得衍生物Cu@C,也用于催化苯甲醇氧化反应.结果表明:Cu@C催化剂重复使用5次,可维持较高的苯甲醇转化率,但苯甲醛选择性有所下降.用X射线衍射(XRD)、N2物理吸附(BET)、热分析(TG-DSC)、红外光谱(FTIR)、能量色散X射线光谱分析(EDX)等技术对催化剂进行了结构表征,发现:Cu@C在反应中生成的Cu2O促进了苯甲醛的深度氧化. 相似文献
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高钛Ti-MCM-41分子筛的合成、表征与催化氧化性能考察 总被引:1,自引:0,他引:1
以硅酸钠、三氯化钛为原料,在Si/Ti物质的量的比为2~60的范围内合成出了Ti-MCM-41分子筛。采用XRD,FTIR,UV-Raman,TEM,低温N2吸附等对合成的Ti-MCM-41进行了表征;并以环己烯的氧化为探针反应,对其催化氧化性能进行了考察。结果表明:合成的Ti-MCM-41介孔分子筛在nSi/nTi=4时,仍然保持了MCM-41的介孔结构,而当Si/Ti物质的量的比为2时,介孔结构消失;在制备过程中对pH值的适时调节,使硅酸钠和三氯化钛得到充分的水解和混合,制备出了高钛Ti-MCM-41分子筛,同时又避免了混合凝胶在水热反应过程中pH值升高的问题。实验发现,随着分子筛中钛含量的增加,环己烯在H2O2体系中的氧化转化率增大,最高约为83%,氧化环己烷的收率先增大后减小,最大约为37%;1,2-环己二醇的收率逐渐增大,最大约为57%。 相似文献
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Shuifa Qiu Yunyang Wei Prof. Dr. Guosheng Liu Prof. Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2009,15(12):2751-2754
Taking the air! A PdII‐catalyzed intramolecular hydroamination of allenes coupled to alcohol oxidation has been developed. This reaction is performed by using a nitrogen‐based ligand under aerobic conditions, under which the molecular oxygen is used as the terminal oxidant for the reoxidation of Pd0 species to complete the catalytic cycle.