RaneyR Type Nickel Catalysts From Rsr Atomization Of Al-Ni Powders

1981 ◽  
Vol 8 ◽  
Author(s):  
C. S. Brooks ◽  
F. D. Lemkey ◽  
G. S. Golden

ABSTRACTThe synthesis and catalytic properties of hydrogenation catalysts of the RaneyR type derived from aluminum-nickel and aluminum-molybdenum-nickel RSR alloy powders have been evaluated. Two binary aluminum-nickel alloys, RSR 588, with 50 w/o Ni corresponding to currently available RaneyR commercial alloys, and RSR 587, with 28.5 w/o Ni corresponding to the proeutectic composition which produces exclusively Al3Ni as the precursor phase, were synthesized. One ternary, RSR 589, aluminum-molybdenum-nickel alloy with a nickel and molybdenum content to correspond to a commercial promoted RaneyR alloy was prepared.The hydrogenation catalytic activity for six organic compounds representing diverse functionalities was measured in a bench scale batch liquid slurry catalytic reaction. Each catalyst was suspended in an agitated solution of the reaction (0.8 to 5M) at 22°C under a constant hydrogen over pressure of 0.86 atmospheres. A declining pressure technique was also used as a measure of catalytic activity where the catalyst was suspended in an agitated solution of the three reactants at 80°C at an initial hydrogen pressure of four atmospheres. The reactants selected consisted of acetone, nitrobenzene, itaconic acid, butyronitrile, toluene, and dextrose. The organic functionalities hydrogenated consisted of the conversion of:(1) Carbonyl to alcohol(2) Nitro group to amine group(3) Double carbon bond to a single carbon bond(4) Nitrile group to an amine group(5) Aromatic to a hydroaromatic ring(6) Aldehyde to an alcohol.RSR 587 catalyst, containing 28.5 w/o nickel, provides superior hydrogenation rates over bulk cast RaneyR nickel catalysts by factors ranging from 2 to 20 for selected reactions. Rapid solidification followed by heat treatmen0t at 850°C of Al ∼42 w/o Ni powders yielded the greatest specific catalytic activity and provides a unique enrichment path for the formation of the peritectic phase, A13Ni, and subsequently the most active skeletal nickel pore structure with the least amount of waste aluminum.

2021 ◽  
Author(s):  
Israel T. Pulido-Díaz ◽  
Alejandro Serrano-Maldonado ◽  
Carlos César López-Suárez ◽  
Pedro A. Méndez-Ocampo ◽  
Benjamín Portales-Martínez ◽  
...  

RhNPs supported on mesoporous silica functionalized with nicotinamide groups provided active hydrogenation catalysts for several functional groups, wherein the shape and size of the RhNPs are maintained after catalysis.


1974 ◽  
Vol 139 (4) ◽  
pp. 834-850 ◽  
Author(s):  
Jay C. Unkeless ◽  
Saimon Gordon ◽  
E. Reich

Cultured thioglycollate-stimulated peritoneal macrophages synthesize, accumulate, and continuously release high levels of plasminogen activators for at least 4 days whereas cultures of unstimulated macrophages do not; the higher specific catalytic activity of released vs. cell-associated enzyme suggests that the plasminogen activators are actively secreted. The major macrophage plasminogen activator is a serine protease of mol wt 48,000, and thus resembles the comparable enzyme released by virally transformed fibroblasts. Macrophages release a second plasminogen activator of mol wt 28,000 that is also a serine enzyme. The secretion products released by stimulated and unstimulated macrophages have been compared by SDS-polyacrylamide gel electrophoresis after chemical labeling with 3H-DFP or biosynthetic labeling with 14C-amino acids. These procedures show that some proteins are formed in both cultures, whereas others are uniquely secreted by each type of macrophage. The serine enzymes released by the two kinds of macrophages differ in specificity and electrophoretic mobility.


e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
Inês Matos ◽  
Auguste Fernandes ◽  
Rita Catalão ◽  
Ana M. Botelho do Rego ◽  
José R. Ascenso ◽  
...  

AbstractIn this paper we present two different techniques for the preparation of single site heterogeneous catalyst. The first method consists in the impregnation of a solution of the organometallic compound in MCM41. The second method intends to establish the in situ synthesis of the complex within the solid’s pores by the reaction of the organic ligand with the metal cation previously introduced in the support. The direct deposition of the organometallic complex in the support resulted in an active catalyst which gives polyethylene with the same microstructure as the one obtained with the related homogeneous systems. The heterogeneous catalysts obtained by reaction of the ligand with the metal already present in the support showed a lower catalytic activity.


2009 ◽  
Vol 1 (5) ◽  
pp. 397-402 ◽  
Author(s):  
Kimihisa Yamamoto ◽  
Takane Imaoka ◽  
Wang-Jae Chun ◽  
Osamu Enoki ◽  
Hideaki Katoh ◽  
...  

2010 ◽  
Vol 2 (9) ◽  
pp. 789-789 ◽  
Author(s):  
Kimihisa Yamamoto ◽  
Takane Imaoka ◽  
Wang-Jae Chun ◽  
Osamu Enoki ◽  
Hideaki Katoh ◽  
...  

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