The Polymer-Protected Pd–Pt Bimetallic Clusters Having Catalytic Activity for Selective Hydrogenation of Diene. Preparation and EXAFS Investigation on the Structure

1990 ◽  
Vol 19 (5) ◽  
pp. 815-818 ◽  
Author(s):  
Naoki Toshima ◽  
Tetsu Yonezawa ◽  
Masafumi Harada ◽  
Kiyotaka Asakura ◽  
Yasuhiro Iwasawa
2019 ◽  
Vol 55 (3) ◽  
pp. 373-376 ◽  
Author(s):  
Weijun Zhou ◽  
Youxing Fang ◽  
Jiangtao Ren ◽  
Shaojun Dong

Illustrative pathways for the preparation of bimetallic nanoclusters using DNA-AgNC, and a schematic representation of the reduction of 4-NP to 4-AP in the presence of DNA-AgNC or bimetallic nanoclusters.


2019 ◽  
Vol 43 (10) ◽  
pp. 4253-4260 ◽  
Author(s):  
Gauravjyoti D. Kalita ◽  
Podma P. Sarmah ◽  
Pallab Kr. Saikia ◽  
Lakshi Saikia ◽  
Pankaj Das

A simple and facile approach for the synthesis of tunable ligand-assisted Pd nanoparticles for selective hydrogenation of nitroarenes.


ChemInform ◽  
2011 ◽  
Vol 42 (16) ◽  
pp. no-no
Author(s):  
Minkyung Lim ◽  
Kathlia A. De Castro ◽  
Seungchan Oh ◽  
Kangsuk Lee ◽  
Young-Wook Chang ◽  
...  

2021 ◽  
Author(s):  
Jianguo liu ◽  
Jiangmin Sun ◽  
Longlong Ma

The development of high efficiency, excellent selectivity, and super activity metal catalyst for chemical selective hydrogenation of alkynes to olefin is of great significance in the field of the chemical industry. At the same time, the development of a large number of available base metal catalysts for organic conversion remains an important objective of chemical research. Herein, we report a facile preparation of a simple, high catalytic activity, environmentally friendly, and inexpensive biomass carbon material supported nano-nickel catalyst from lignin residue. The entire preparation process of the catalyst is simple, reliable, economical, and environmentally friendly, which provides a potential utilization prospect for large-scale industrial applications of biomass-based carbon material catalysts. Biomass-based lignin residues can not only reduce the high oxidation state of nickel ions into nickel nanoparticles by the in-situ reducing gas generated during the calcination process, but the mesoporous structure of lignin residue also promotes the adsorption of nickel metal, which greatly improved the catalytic activity of biomass-based Ni-based catalysts. The simple synthetic green, cost-effective and sustainable biomass-based Ni-based catalyst shows good performance in the selective hydrogenation of phenylacetylene, reaching 97.2% conversion and 84.3% styrene selectivity, respectively.


2020 ◽  
Vol 10 (24) ◽  
pp. 8421-8428
Author(s):  
V. Sudheeshkumar ◽  
Maryam Alyari ◽  
Mahesh Gangishetty ◽  
Robert W. J. Scott

AgPd bimetallic clusters dispersed in a silica matrix were made by a top down synthetic strategy and used as selective hydrogenation catalysts.


2015 ◽  
Vol 17 (8) ◽  
pp. 4178-4182 ◽  
Author(s):  
Li Peng ◽  
Jianling Zhang ◽  
Shuliang Yang ◽  
Buxing Han ◽  
Xinxin Sang ◽  
...  

Here a Pd/ionic liquid/metal–organic framework catalyst is developed, which shows high activities in catalyzing the selective hydrogenation of alkynes under mild conditions.


2011 ◽  
Vol 393-395 ◽  
pp. 1185-1188
Author(s):  
Chang You Li ◽  
Xiao Yan Li ◽  
Yi Fei Guo

Cu-Zn-Al catalyst was modified by the additives such as Ni and Mn, and the prepared catalyst was employed in the selective catalytic hydrogenation of cinnamaldehyde. The results showed that the addition of Ni could improve catalytic activity significantly, moreover, the improving effect was highest when Zn was replaced by Ni, simultaneously leading to excessive hydrogenation. The Cu-(5%)Mn-Zn-Al catalyst exhibited a higher selectivity of 93.6% for C = O bond to cinnamyl alcohol and hydrogenation activity of 33.0% conversion at 130°C under 1.0 MPa of H2 pressure with the reaction time of 1 h. TPR and XRD characterization showed that Mn promoter was favorable for the growth of Cu0 fine grains on the surface of catalyst, which not only led to steric effect which improved the selectivity for cinnamyl alcohol, but also reduced the numbers of active centers, consequently decreased the reaction rate.


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