Oxidative acetoxylation of propylene in the presence of palladium catalysts

1981 ◽  
Vol 30 (7) ◽  
pp. 1186-1190 ◽  
Author(s):  
S. F. Politanskii ◽  
A. M. Shkitov ◽  
E. S. Shpiro ◽  
G. V. Antoshin ◽  
Kh. M. Minachev ◽  
...  
Keyword(s):  
Palladium Catalysts ◽  
Oxidative Acetoxylation

ChemInform Abstract: OXIDATIVE ACETOXYLATION OF METHYL OLEATE WITH PALLADIUM CATALYSTS

1976 ◽  
Vol 7 (6) ◽  
pp. no-no
Author(s):  
E. N. FRANKEL ◽  
W. K. ROHWEDDER ◽  
W. E. NEFF ◽  
D. WEISLEDER
Keyword(s):  
Methyl Oleate ◽  
Palladium Catalysts ◽  
Oxidative Acetoxylation

Oxidative acetoxylation of propylene in the presence of palladium catalysts

1981 ◽  
Vol 30 (7) ◽  
pp. 1180-1185 ◽  
Author(s):  
S. F. Politanskii ◽  
A. M. Shkitov ◽  
V. V. Kharlamov ◽  
Kh. M. Minachev ◽  
I. I. Moiseev ◽  
...  
Keyword(s):  
Palladium Catalysts ◽  
Oxidative Acetoxylation

scholarly journals Oxidative Acetoxylation of Toluene and Benzene over Supported-Palladium Catalysts.

1993 ◽  
Vol 36 (3) ◽  
pp. 235-238
Author(s):  
Masahiko MATSUKATA ◽  
Korekazu UEYAMA ◽  
Kimikazu KITAKADO ◽  
Toshinori KOJIMA
Keyword(s):  
Palladium Catalysts ◽  
Supported Palladium Catalysts ◽  
Supported Palladium ◽  
Oxidative Acetoxylation

Oxidative acetoxylation of methyl oleate with palladium catalysts

1975 ◽  
Vol 40 (22) ◽  
pp. 3247-3253 ◽  
Author(s):  
Edwin N. Frankel ◽  
William K. Rohwedder ◽  
William E. Neff ◽  
David Weisleder
Keyword(s):  
Methyl Oleate ◽  
Palladium Catalysts ◽  
Oxidative Acetoxylation

Model reactions for the study of hydrogenation and acidic activity of palladium catalysts

1987 ◽  
Vol 52 (8) ◽  
pp. 2019-2027 ◽  
Author(s):  
Libor Červený ◽  
Nguyen Thi Du ◽  
Ivo Paseka
Keyword(s):  
Palladium Catalysts ◽  
Styrene Oxide ◽  
Side Reactions ◽  
Pd Catalysts ◽  
Variable Parameters ◽  
Acid Properties ◽  
Liquid Phase Hydrogenation ◽  
Acid Catalysed Reactions ◽  
Different Content ◽  
Model Reactions

Palladium catalysts have been used to study the hydrogenation of 1-phenyl-2-butene-1-ol which is accompanied by several side reactions considered to be acid-catalysed. Another model reaction studied was dehydration and subsequent hydrogenation or hydrogenolysis of 1-phenyl-1,3-propanediol to 3-phenyl-1-propanol, accompanied by formation of propylbenzene. The dehydration and propylbenzene formation can be again classified as acid-catalysed reactions. Another one is methanolysis of styrene oxide taking place under conditions of liquid phase hydrogenation due to the acid properties of Pd-H systems. Hydrogenation activity of Pd catalysts was tested by hydrogenation of cyclohexene. Sixteen Pd catalysts on different supports and with different content of active component were used, their activity and selectivity was determined and the effect of variable parameters in the synthesis of these catalysts on the activity and selectivity is discussed.

Attaching Palladium Catalysts to Antibodies

2021 ◽  
pp. 116298
Author(s):  
Paul Cowling ◽  
Mark Bradley ◽  
Annamaria Lilienkampf
Keyword(s):  
Palladium Catalysts

scholarly journals Sintering Activated Atomic Palladium Catalysts with High-Temperature Tolerance of ∼1,000°C

2020 ◽  
pp. 100287
Author(s):  
Nating Yang ◽  
Yonghui Zhao ◽  
Hao Zhang ◽  
Weikai Xiang ◽  
Yuhan Sun ◽  
...  
Keyword(s):  
High Temperature ◽  
Palladium Catalysts ◽  
Temperature Tolerance ◽  
High Temperature Tolerance

scholarly journals Development of Highly Efficient, Glassy Carbon Foam Supported, Palladium Catalysts for Hydrogenation of Nitrobenzene

Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1172
Author(s):  
Ádám Prekob ◽  
Mahitha Udayakumar ◽  
Gábor Karacs ◽  
Ferenc Kristály ◽  
Gábor Muránszky ◽  
...  
Keyword(s):  
Zeta Potential ◽  
Glassy Carbon ◽  
Palladium Nanoparticles ◽  
Palladium Catalysts ◽  
Sucrose Solution ◽  
Supported Catalyst ◽  
Carbon Foam ◽  
Hydroxyl Groups ◽  
Polyurethane Elastomers ◽  
Oh Groups

Glassy carbon foam (GCF) catalyst supports were synthesized from waste polyurethane elastomers by impregnating them in sucrose solution followed by pyrolysis and activation (AC) using N2 and CO2 gas. The palladium nanoparticles were formed from Pd(NO3)2. The formed palladium nanoparticles are highly dispersive because the mean diameters are 8.0 ± 4.3 (Pd/GCF), 7.6 ± 4.2 (Pd/GCF-AC1) and 4.4 ± 1.6 nm (Pd/GCF-AC2). Oxidative post-treatment by CO2 of the supports resulted in the formation of hydroxyl groups on the GCF surfaces, leading to a decrease in zeta potential. The decreased zeta potential increased the wettability of the GCF supports. This, and the interactions between –OH groups and Pd ions, decreased the particle size of palladium. The catalysts were tested in the hydrogenation of nitrobenzene. The non-treated, glassy-carbon-supported catalyst (Pd/GCF) resulted in a 99.2% aniline yield at 293 K and 50 bar hydrogen pressure, but the reaction was slightly slower than other catalysts. The catalysts on the post-treated (activated) supports showed higher catalytic activity and the rate of hydrogenation was higher. The maximum attained aniline selectivities were 99.0% (Pd/GCF-AC1) at 293 K and 98.0% (Pd/GCF-AC2) at 323 K.

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