529 resultados para GOLD CATALYST
Resumo:
A new copper-(Schiff-base) complex, derived from (S)-2-amino-1,1-di(3,5-di-t-butylphenyl)propanol, 2-hydroxy-5-nitrobenzaldehyde and copper acetate monohydrate, was used as an efficient catalyst for the cyclopropanation of styrene with diazoacetates, affording ees of up to 98%. (C) 2000 Elsevier Science Ltd. All rights reserved.
Resumo:
A zirconium-based Ziegler-Natta catalytic system has been tested in the dimerization of 1-butene. It was found that the concentration of Et2AlCl, Ph3P and PhONa as well as the reaction temperature had great influences on the activity and selectivity of the catalyst. Under the optimum reaction conditions, the conversion of 1-butene is 91.9%, and the selectivity of dimers is 76.7%. Basic ligands such as Ph3P and PhONa can inhibit isomerization of 1-butene to 2-butene effectively. In addition, the metal hydride mechanism was also suggested and some indirect evidence was obtained in favor of this mechanism.
Resumo:
考察了陈化温度对新癸酸钕(简称Nd)、氢化二异丁基铝(简称Al)和氯化二异丁基铝(简称Cl)组成的催化剂共聚合丁二烯-异戊二烯的影响。结果表明,催化剂的陈化温度对聚合产物的相对分子质量分布有明显的影响,采用较高陈化温度(50℃)所得催化剂,在催化剂3组分的加入顺序为Al、Cl、Nd或Cl、Nd、Al时,可获得窄相对分子质量分布(小于3.00)共聚物;催化剂3组分的加入顺序和陈化温度对共聚物的微观结构影响不大,2种单体单元的顺式-1,4-结构摩尔分数均在98%以上
Resumo:
We present a newly designed colormetric sensor sensitive to pH value based on a gold nanocomposite composed of gold nanoparticles and pH-sensitive polymer{dodecylthioether end functionalized poly[2-(diethlamino) ethyl methacrylate], poly(DEAEMA)-DDT}. We have shown that this design can produce stable GNP precipitate under weakly basic condition(pH=7.5) and this precipitate can be dispersed in acidic solution(pH=4.0), due to the 2-(diethylamino) ethyl methacrylate protonated by H+.
Resumo:
Hybrid materials of polyacrylamide networks and gold nanoparticles were prepared by directly heating an aqueous solution containing HAuCl4, acrylamide, N,N'-methylenebisacrylamide, and sodium sulfite (Na2SO3). Acrylamide, N,N'-methylenebisacrylamide, and Na2SO3 were used as monomers, crosslinking agent, and initiator, respectively.
Resumo:
It was reported for the first time that the electrocatalytic activity of the Carbon-supported Pd-Ir (Pd-Ir/C) catalyst with the suitable atomic ratio of Pd and Ir for the oxidation of formic acid in the direct formic acid fuel cell (DFAFC) is better than that of the Carbon-supported Pd (Pd/C) catalyst, although Ir has no electrocatalytic activity for the oxidation of formic acid. The potential of the anodic peak of formic acid at the Pd-Ir/C catalyst electrode with the atomic ratio of Pd and Ir = 5:1 is 50 mV more negative than that and the peak current density is 13% higher than that at the Pd/C catalyst electrode.