共查询到20条相似文献,搜索用时 12 毫秒
1.
Skupińska Jadwiga Karpińska Monika Ołówek Maria Kasprzycka-Guttman Teresa 《Central European Journal of Chemistry》2005,3(1):28-39
The PdCl2/Fe/I2/Py catalytic system (Py-pyridine), reported to be highly active in the reaction of nitrobenzene carbonylation to ethyl phenylcarbamate
was studied. The present paper describes the role of catalyst components and its effect on the activity and selectivity of
the catalyst. The increase in the amount of PdCl2 in the system while retaining a constant level of the other catalyst components, results in the increase of both carbamate
and aniline yields. The increase in the amount of iron while retaining the other components constant, initially causes an
increase in the carbamate yield; however, at Fe: Pd ratios higher than 36, the carbamate yield remains constant. The change
in the amount of iron has no effect on the amount of aniline formed in the system. An increase in the amount of iodine in
the system while retaining the other components constant, results in a decrease in carbamate yield and a considerable increase
in the aniline yield of the reaction products. 相似文献
2.
在H2O-alcohol体系中通过Pd/C催化的还原偶联反应由杂环芳卤高收率的得到了二芳基化合物. 该方法操作简单, 环境友好, Pd/C可重复使用, 无需相转移催化剂也能得到较高收率. 讨论了醇、碱的种类和用量以及不同底物对反应收率的影响. 相似文献
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High‐yield reductive homocoupling of benzotrichloride and benzal chloride followed by consecutive reductive dechlorination to 1,2‐dichlorostilbene and stilbene is effected in the presence of sodium formate as the reducing agent and Pd/C catalysts. 相似文献
5.
Reductive carbonylation of aryl and heteroaryl iodides using Pd(acac)2/dppm as an efficient catalyst
Abhilash S. SinghBhalchandra M. Bhanage Jayashree M. Nagarkar 《Tetrahedron letters》2011,52(18):2383-2386
Palladium catalyzed simple and efficient protocol for reductive carbonylation of aryl and heteroaryl compounds has been developed. The formylation of aryl and heteroaryl iodides takes place in the presence of Pd(acac)2/dppm catalyst at 10 bar pressure of synthetic gas to give the desired aromatic and heteroaromatic aldehydes in good to excellent yields. Easy work-up, stability of the catalyst, low catalyst loading and less reaction time are the advantages of this method. 相似文献
6.
Antal Sárkány 《Reaction Kinetics and Catalysis Letters》2001,74(2):299-307
Selectivity of product formation has been tested in hydrogenation of acetylene over 0.3 wt.% Pd/-alumina and 0.5 wt.% Pd/TiO2catalysts. Non-steady-state regime of catalyst operation was tested in pulse-flow experiments. Significant carbon poisoning appears to be a necessaryrequisite for selective formation of ethylene. The effect of hydrogen and acetylene partial pressure has been tested on the selectivity of C4products. At 273–298 K the catalysts showed 26–35% selectivity for C4 hydrocarbons and <2.5% for ethane production at conversionsof 30–40%. Deuterium distribution in ethylene and 1,3-butadiene and the deuterium content of the surface hydrogen pool have been compared and mechanismof diene formation has been discussed. 相似文献
7.
以胶原纤维(CF)接枝表棓儿茶素棓酸脂(EGCG)为载体,制备了新型非均相钯(Pd)纳米催化剂(CF-EGCG-Pd).EGCG作为"桥分子"不仅对Pd纳米颗粒具有锚定作用,而且能控制Pd纳米颗粒的大小及分布.通过SEM、TEM、XRD、XPS对该催化剂的形貌和物理特性能进行了表征,发现该催化剂具有规整的纤维结构,在胶原纤维的外表面形成了高分散的平均粒径在3.8 nm的Pd纳米颗粒.将该催化剂用于硝基苯液相催化加氢反应,结果表明在308 K和1.0 MPa氢压下,硝基苯转化速率(TOF)达到34.13 mol·mol-1·min-1,苯胺选择性为100%,催化剂重复使用3次其催化活性基本不变. 相似文献
8.
利用Zn2+和2-甲基咪唑自组装形成的ZIF-8, 800℃N2氮气气氛下焙烧得到Zn/C-N载体.采用NaBH4还原法将不同含量Pd负载于Zn/C-N上焙烧后得到Pd/Zn/C-N催化剂, ICP测得Pd实际负载量为0.02%、0.05%、0.1%、0.3%.负载Pd后,由于Pd氢溢流作用, ZnO表面还原温度降低,氧空穴增加,更有利于CO2解离吸附,因此Pd负载量越高,催化剂CO2转化率越高.甲醇选择性受Pd纳米颗粒大小显著影响,小颗粒Pd与ZnO相互作用更强,更有利于甲醇生成,其中0.02%Pd/Zn/C-N催化剂在275℃, 2 MPa反应条件下, Pd/g上甲醇时空收率最高, STYMeOH值为11.0 mol/(g Pd·h). 相似文献
9.
Pd/ZrO2是甲烷低温燃烧研究较为广泛的催化剂,其中载体ZrO2对稳定PdO起到了重要作用。 采用水热法合成了纯相的M-ZrO2和T-ZrO2,然后采用浸渍法制备了Pd/M-ZrO2和Pd/T-ZrO2催化剂,并考察了不同晶型ZrO2对催化剂的活性和稳定性的影响。 结果表明,Pd/M-ZrO2催化剂的活性和稳定性明显优于Pd/T-ZrO2。 结合XRD、TEM和TPO表征结果,发现Pd/M-ZrO2活性高的原因是PdO分散性更好,Pd/M-ZrO2较好的稳定性与PdO和ZrO2的作用方式有关。 相似文献
10.
A novel type of heterogenized CuCl2 catalysts was designed for the oxidative carbonylation of methanol to dimethyl carbonate (DMC) taking account of the plausible reaction mechanism and intermediates. To prevent severe corrosion of the reaction equipment materials due to Cl– while keeping the catalytic activity of the homogeneous CuCl2 catalyst, we adopted, as supports (or ligands) of CuCl2, four polymers, bearing a 2,2-bipyridine (bpy) or pyridine (py) unit, namely, poly(2,2-bipyridine-5,5-diyl) (Pbpy), poly(pyridine-2,5-diyl) (Ppy), poly(N,N-bisphenylene-2,2-bipyridine-4,4-dicarboxylic amide) (Bpya), and poly(4-methyl-4-vinyl-2,2-bipyridine) (Pvbpy), together with one chelate compound, 8-quinolinol. The catalytic activity, stability of heterogenized CuCl2 and their corrosivities to stainless steels were examined in the liquid-phase reaction of the oxidative carbonylation of methanol. These polymer-supported catalysts showed considerable catalytic activity and stability for the DMC synthesis. In particular, the Pbpy-CuCl2 and Ppy-CuCl2 catalysts exhibited high DMC yields and selectivity comparable to those of the homogeneous CuCl2 catalyst. This high activity appears to be associated with the presence of the -conjugated system in the polymers, which affect the redox reactions of Cu involved in the catalytic reaction. All of the polymer-supported CuCl2 catalysts could be easily recycled after filtration, and the initial catalytic activity was maintained after three times of use. The corrosive characters of the catalysts were closely related to CuCl2 leaching from the supports, which reflects the ability of supports to coordinate Cu. These experimental results suggest that both the electronic structure and the coordination ability of the polymer supports are key factors for the development of an effective catalytic system. 相似文献
11.
The catalytic activity of Pd/Co3O4 toward methane oxidation has been examined in this study as a function of Pd loading, reaction temperature, space velocity
and methane concentration in the reaction gas mixture. The bare oxide is quite active achieving a 100% methane conversion
at 480°C under the reaction conditions used. The catalyst with the highest Pd loading tested of 10 wt.% yields the best activity
curve, but the 5 wt.% Pd/Co3O4 catalyst performs nearly as well. Complete conversion for this catalyst is attained at 300°C and the activity remains stable
over a 90-min test period. 相似文献
12.
采用溶胶凝胶法和浸渍法制备了负载于蜂窝陶瓷上的Co/Fe/Al2O3/cordierite催化剂,在陶瓷管流动反应器上对其催化C3H6选择性还原NO的性能进行了测试。结果表明,该催化剂表现出最优脱硝性能,在模拟烟气条件下,当反应温度为550 ℃时可实现97%的脱硝效率。Co的引入可显著增强Fe/Al2O3/cordierite催化剂抗SO2和H2O的能力。在模拟烟气中同时引入0.02% SO2和3% H2O后,1.5Co/Fe/Al2O3/cordierite的脱硝性能受影响甚微,当反应温度高于500 ℃时1.5Co/Fe/Al2O3/cordierite催化C3H6还原NO的效率均可达到90%以上;相比之下,未经Co修饰的催化剂Fe/Al2O3/cordierite脱硝性能受到了严重的抑制,在整个反应温度区间(200-700 ℃)内,其催化C3H6还原NO的效率最高不足50%。XRD和SEM表征结果表明,经过适量的Co修饰后的1.5Co/Fe/Al2O3/cordierite表面变得更疏松,且形成了以钴铁和钴铝双金属氧化物为主要成分的球状晶粒。H2-TPR结果表明,相比于Fe/Al2O3/cordierite,1.5Co/Fe/Al2O3/cordierite有更好的低温还原性能。Py-FTIR结果表明,Co的引入可使催化剂表面的Lewis酸明显增加,且生成了Brønsted酸。N2吸附-脱附表征结果表明,Co可增大催化剂的比表面积。 相似文献
13.
Magne O. Sydnes 《Tetrahedron letters》2008,49(7):1199-1202
A range of different nitro aryls were converted in one-pot to the corresponding secondary alkyl amino aryls in good to excellent yields by using aldehydes as alkyl source and hydrogen over Pd/C (10%) as reducing agent. In all examples, but one, the secondary amine was the sole alkylation product isolated. When formaldehyde was used as the alkyl source, substantial amount of the corresponding tertiary amine was isolated, however, by altering the reaction conditions slightly the corresponding secondary amine could be isolated in superb yield. 相似文献
14.
Kebin Zhou Hongde Chen Qun Tian Dixin Shen Xiaobai Xu 《Reaction Kinetics and Catalysis Letters》2002,77(1):65-72
Pd/LaFe0.8Co0.2O3 was found to be more active than the Pd/Al2O3 catalyst in propane oxidation. Activity and the oxidation state of palladium were strongly affected by the redox ratio (S) of reactants. Higher propane conversion could be obtained under rich conditions at higher temperatures, contributing to steam reforming. The presence of excess steam would bring about inhibition and oscillation. 相似文献
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采用浸渍法制备了Pd质量分数为0.1%~1.0%的Pd/SiO2和Pd/5%CexZr1-xO2/SiO2(x0.0~1.0)系列催化剂,在微型固定床反应器上对催化剂的甲烷催化燃烧性能进行了评价,用XRD、H2-TPR等分析测试技术对催化剂的结构进行了表征。结果表明,Pd/SiO2和Pd/CexZr1-xO2/SiO2催化剂都具有较好的甲烷催化燃烧活性,CexZr1-xO2可以明显提高催化剂的催化活性,并且Ce和Zr的比值对催化剂催化活性也有显著的影响。XRD和TPR显示,Pd/CexZr1-xO2/SiO2催化剂中的CexZr1-xO2对PdO的分散性和还原性有较好的促进作用。 相似文献
17.
Belinda T. Lee 《Tetrahedron》2004,60(34):7391-7396
(PCy3)2Cl2RuCHPh-catalyzed Kharasch additions of trihaloalkanes across olefins provide polyhalogenated adducts, which upon hydrolysis furnish α,β-unsaturated ketones, aldehydes, or γ-hydroxybutenolides. This two-step process represents an overall acylation or carbonylation of an olefin. 相似文献
18.
Shuangshuang Fan Jianhua Yi Li Wang Zhentao Mi 《Reaction Kinetics and Catalysis Letters》2007,92(1):175-182
Pd/Al2O3 catalysts were prepared by the impregnation method and were used for the direct formation of hydrogen peroxide from H2 and O2. The H2O2 concentration and selectivity were strongly dependent on the solubility of hydrogen in the reaction medium. The modification
of the support by halogenate has a beneficial effect on the selectivity. The state of the active Pd on Pd/Al2O3 catalysts was studied using X-ray photoelectron spectroscopy, and Pd(0) was found to be active. 相似文献
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采用等体积共浸渍法制备了一系列Pd-Ag/CeO2-ZrO2-La2O3-Al2O3催化剂。运用N2吸附-脱附,X射线衍射(XRD),H2程序升温还原(H2-TPR),紫外-可见漫反射光谱(UV-Vis DRS),X射线光电子能谱(XPS)对催化剂进行表征,并考察其对甲醇的催化氧化性能。活性测试结果表明,Ag的添加可显著改善Pd催化剂对甲醇的催化氧化活性,T50、T90以及ΔT分别为125℃,150℃和25℃,具有较好的应用前景。H2-TPR表明,引入Ag可明显改善催化剂的还原性能,使表面易还原氧物种量增多,还原速率加快;UV-Vis DRS及XPS表明,Pd、Ag金属之间以及金属与载体之间存在电子效应,这种效应促使金属与载体界面产生大量具有活性的氧物种,不仅提高了催化剂的低温活性,还提高了催化剂的氧化速率。 相似文献