Effect of Ni-Al Precursor Alloy on the Catalytic Activity for a Raney-Ni Cathode

2000 ◽  
Vol 147 (6) ◽  
pp. 2242 ◽  
Author(s):  
Shin-ichi Tanaka ◽  
Norimitsu Hirose ◽  
Toshiyuki Tanaki ◽  
Yukio H. Ogata
Keyword(s):  
Catalytic Activity ◽  
Raney Ni ◽  
Precursor Alloy

Effect of MgO Addition on the Properties of Ni/Al2O3 and Its Catalytic Activity in Hydrogenation of N-(2`,3`-dimethoxy benzyl)-3,4-dioxy-methylene-phenylethylamine

2019 ◽  
Vol 41 (5) ◽  
pp. 796-796
Author(s):  
Guosheng Wang Guosheng Wang ◽  
Xinxin Zhao and Siyu Han Xinxin Zhao and Siyu Han
Keyword(s):  
Catalytic Activity ◽  
Surface Area ◽  
Pore Diameter ◽  
Supported Catalysts ◽  
Bet Surface Area ◽  
High Catalytic Activity ◽  
Average Pore ◽  
Secondary Reactions ◽  
Al2o3 Support ◽  
Raney Ni

the nickel based alumina-supported catalysts modified or promoted by magnesia were prepared by wet impregnation and successfully used for hydrogenation of N-(2`,3`-dimethoxy benzyl)-3,4-dioxy-methylene-phenylethylamine, the 20Ni-6MgO/74Al2O3 samples exhibits the highest BET surface area, the largest pore volume, and the largest pore diameter in all of the samples such as Ni/Al2O3 and 20Ni-xMgO(80-x)Al2O3 excepted the highest BET surface area of Ni/Al2O3. the average pore diameter of the 20Ni-6MgO/74Al2O3 samples were two times as large as Ni/Al2O3, it was indicated that the function of expanding role or the mesoporosity was increased by addition of MgO, and MgO might be regarded as pore-enlarge agent for the bare Al2O3 support and benefit for the transport of large molecules reactants and products The weak formation of MgO-Al2O3 and MgO-NiO solid solution as a result of competing interaction of MgO with Al2O3 support and NiO precursors restrained the strong interaction of NiO species with Al2O3 support, which favored the dispersion of active Ni centers and improved the reducible degree of NiO species on the surface of the catalysts. The improvement of basicity or the decrease in the number of acid centers in the catalysts avoid the secondary reactions, and subsequently resulted in high catalytic activity. The utilization of meso-porous 20Ni-6MgO/74Al2O3 for catalytic hydrogenation of N-(2`,3`-dimethoxy benzyl)-3,4-dioxy-methylene-phenylethylamine(Shiff’s base) with the highest selectivity of 99.70% and yields of 94.36% implied that the instead of Raney Ni was feasible.

Facile Fabrication of Nanosized Nickel Powder via Solid-State Reaction at Low Heat and its Catalytic Performance

2011 ◽  
Vol 393-395 ◽  
pp. 1235-1241
Author(s):  
Liu Hong ◽  
Wu Bin ◽  
Feng Cheng Tao ◽  
Qin Xia
Keyword(s):  
Catalytic Activity ◽  
Solid State ◽  
Solid State Reaction ◽  
Photoelectron Spectroscopy ◽  
Catalytic Performance ◽  
X Ray ◽  
Nickel Powders ◽  
Transmission Electron ◽  
Raney Ni ◽  
Facile Fabrication

Nano-Nickel (Ni0) powders have been successfully prepared via the reduction of nanosized NiO powders by the solid state reaction. And the nanosized NiO powders were derived from low temperature (350°C) calcinations in muffle in air of nanosized Ni(OH)2 powders firstly prepared by the room temperature solid state reaction between NiSO4•6H2O and NaOH by H2 at 400°C for 4 h. The crystallinity, microstructure of surface and xps property of obtained nickel powders were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). Furthermore, the catalytic activity of the obtained nanosized Ni powders for hydrogenation of nitrobenzene to aniline was investigated. The results show that the spherical Ni parepared in particle sizes ranges from 20 to 25 nm and achieves enhanced catalytic activity for hydrogenation of nitrobenzene to aniline compared with Raney Ni.

Reduction of o-Hydromandelic Acid for Preparation of o-Hydrophenylacetic Acid

2013 ◽  
Vol 716 ◽  
pp. 94-97 ◽  
Author(s):  
Yue Zhang ◽  
Xian Xian Shi ◽  
Ya Chen ◽  
Zhen Hua Shang ◽  
Li Qiang Wang
Keyword(s):  
Catalytic Activity ◽  
Optimal Condition ◽  
Metal Catalysts ◽  
Orthogonal Test ◽  
Raney Ni

In this work, reduction of o-hydromandelic acid to o-hydrophenylacetic acid was investigated. Inorganic and metal catalysts were used in the process of reduction to look for a suitable way for transferring o-hydromandelic acid to o-hydrophenylacetic acid. Of all the catalysts, Raney-Ni has the favorable catalytic activity and the orthogonal test was investigated to determine the optimal condition. The yield of o-hydrophenylacetic acid can up to 90%.

High resolution electron microscopy of lanthanum phosphate crystals

1978 ◽  
Vol 36 (1) ◽  
pp. 274-275
Author(s):  
J. C. Wheatley ◽  
J. M. Cowley
Keyword(s):  
Electron Microscopy ◽  
Catalytic Activity ◽  
High Resolution ◽  
Petroleum Industry ◽  
High Resolution Electron Microscopy ◽  
Lanthanum Phosphate ◽  
Good Catalyst ◽  
Resolution Electron ◽  
Good Catalytic Activity ◽  
Physical And Chemical

Rare-earth phosphates are of particular interest because of their catalytic properties associated with the hydrolysis of many aromatic chlorides in the petroleum industry. Lanthanum phosphates (LaPO4) which have been doped with small amounts of copper have shown increased catalytic activity (1). However the physical and chemical characteristics of the samples leading to good catalytic activity are not known.Many catalysts are amorphous and thus do not easily lend themselves to methods of investigation which would include electron microscopy. However, the LaPO4, crystals are quite suitable samples for high resolution techniques.The samples used were obtained from William L. Kehl of Gulf Research and Development Company. The electron microscopy was carried out on a JEOL JEM-100B which had been modified for high resolution microscopy (2). Standard high resolution techniques were employed. Three different sample types were observed: 669A-1-5-7 (poor catalyst), H-L-2 (good catalyst) and 27-011 (good catalyst).

The design and catalytic performance of molybdenum active sites on an MCM-41 framework for the aerobic oxidation of 5-hydroxymethylfurfural to 2,5-diformylfuran

2019 ◽  
Vol 9 (3) ◽  
pp. 811-821 ◽  
Author(s):  
Zhao-Meng Wang ◽  
Li-Juan Liu ◽  
Bo Xiang ◽  
Yue Wang ◽  
Ya-Jing Lyu ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Active Sites ◽  
Aerobic Oxidation ◽  
Catalytic Performance ◽  
Mcm 41

The catalytic activity decreases as –(SiO)3Mo(OH)(O) > –(SiO)2Mo(O)2 > –(O)4–MoO.

Prolonged Expression of Procoagulant Activity of Human Platelets Degranulated by Thrombin

1995 ◽  
Vol 74 (03) ◽  
pp. 958-961 ◽  
Author(s):  
Raelene L Kinlough-Rathbone ◽  
Dennis W Perry
Keyword(s):  
Catalytic Activity ◽  
Thrombus Formation ◽  
Annexin V ◽  
Human Platelets ◽  
Procoagulant Activity ◽  
Prothrombinase Complex ◽  
Arterial Thrombus ◽  
Flowing Blood

SummaryPlatelets are exposed to thrombin when they take part in arterial thrombus formation, and they may return to the circulation when they are freed by fibrinolysis and dislodged by flowing blood. Thrombin causes the expression of procoagulant activity on platelets, and if this activity persists, the recirculating platelets may contribute to subsequent thrombosis. We have developed techniques to degranulate human platelets by treatment with thrombin, and recover them as single, discrete platelets that aggregate in response to both weak and strong agonists. In the present study we examined the duration of procoagulant activity on the surface of thrombin-degranulated platelets by two methods: a prothrombinase assay, and the binding of 125I-labeled annexin. Control platelets generated 0.9 ± 0.4 U thrombin per 107 platelets in 15 min. Suspensions of thrombin-degranulated platelets formed 5.4 ± 0.1 U thrombin per 107 platelets in this time. Binding of 125I-annexin V was also greater with thrombin-treated platelets than with control platelets (controls: 1.7 ±0.1 ng annexin/107 platelets; thrombin-degranulated platelets: 6.8 ± 0.2 ng annexin/107 platelets). With thrombin-degranulated platelets, increased procoagulant activity and annexin binding persisted for at least 4 h after degranulation and resuspension, indicating that the catalytic activity for the prothrombinase complex is not reversed during this time. These platelets maintained their ability to aggregate for 4 h, even in response to the weak agonist, ADP. Thus, platelets that have taken part in thrombus formation and returned to the circulation may contribute to the promotion of further thrombotic events because of the persistence of procoagulant activity on their surface.

Enhanced catalytic activity of low-Pt content nanocatalysts supported on hollow carbon spheres for the ORR in alkaline media

MRS Advances ◽  
2020 ◽  
Vol 5 (57-58) ◽  
pp. 2961-2972
Author(s):  
P.C. Meléndez-González ◽  
E. Garza-Duran ◽  
J.C. Martínez-Loyola ◽  
P. Quintana-Owen ◽  
I.L. Alonso-Lemus ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Anion Exchange ◽  
Average Particle Size ◽  
Synthesis Method ◽  
Alkaline Media ◽  
High Catalytic Activity ◽  
Average Particle ◽  
Carbon Spheres ◽  
Hollow Carbon ◽  
Hollow Carbon Spheres

In this work, low-Pt content nanocatalysts (≈ 5 wt. %) supported on Hollow Carbon Spheres (HCS) were synthesized by two routes: i) colloidal conventional polyol, and ii) surfactant-free Bromide Anion Exchange (BAE). The nanocatalysts were labelled as Pt/HCS-P and Pt/HCS-B for polyol and BAE, respectively. The physicochemical characterization of the nanocatalysts showed that by following both methods, a good control of chemical composition was achieved, obtaining in addition well dispersed nanoparticles of less than 3 nm TEM average particle size (d) on the HCS. Pt/HCS-B contained more Pt0 species than Pt/HCS-P, an effect of the synthesis method. In addition, the structure of the HCS remains more ordered after BAE synthesis, compared to polyol. Regarding the catalytic activity for the Oxygen Reduction Reaction (ORR) in 0.5 M KOH, Pt/HCS-P and Pt/HCS-B showed a similar performance in terms of current density (j) at 0.9 V vs. RHE than the benchmark commercial 20 wt. % Pt/C. However, Pt/HCS-P and Pt/HCS-B demonstrated a 6 and 5-fold increase in mass catalytic activity compared to Pt/C, respectively. A positive effect of the high specific surface area of the HCS and its interactions with metal nanoparticles and electrolyte, which promoted the mass transfer, increased the performance of Pt/HCS-P and Pt/HCS-B. The high catalytic activity showed by Pt/HCS-B and Pt/HCS-P for the ORR, even with a low-Pt content, make them promising cathode nanocatalysts for Anion Exchange Membrane Fuel Cells (AEMFC).

Catalytic Activity of Binary and Triple Systems Based on Redox Inactive Metal Compound, LiSt and Additives of Monodentate Ligands-Modifiers: DMF, HMPA and PhOH, in Selective Ethylbenzene Oxidation with Dioxygen

2016 ◽  
Vol 10 (3) ◽  
pp. 259-270
Author(s):  
Ludmila Matienko ◽  
◽  
Larisa Mosolova ◽  
Vladimir Binyukov ◽  
Gennady Zaikov ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Triple System ◽  
Metal Compound ◽  
Ethylbenzene Oxidation ◽  
Catalytic Systems ◽  
Triple Systems ◽  
Lithium Compound ◽  
Mechanism Of Catalysis ◽  
Monodentate Ligands

Mechanism of catalysis with binary and triple catalytic systems based on redox inactive metal (lithium) compound {LiSt+L2} and {LiSt+L2+PhOH} (L2=DMF or HMPA), in the selective ethylbenzene oxidation by dioxygen into -phenylethyl hydroperoxide is researched. The results are compared with catalysis by nickel-lithium triple system {NiII(acac)2+LiSt+PhOH} in selective ethylbenzene oxidation to PEH. The role of H-bonding in mechanism of catalysis is discussed. The possibility of the stable supramolecular nanostructures formation on the basis of triple systems, {LiSt+L2+PhOH}, due to intermolecular H-bonds, is researched with the AFM method.

Ordered Intermetallic Nanoparticles with High Catalytic Activity Prepared by an Electrochemically Induced Phase Transformation

2019 ◽  
Author(s):  
Du Sun ◽  
yunfei wang ◽  
Kenneth Livi ◽  
chuhong wang ◽  
ruichun luo ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Diffusion Mechanism ◽  
Reduction Reaction ◽  
Atomic Scale ◽  
High Catalytic Activity ◽  
Ambient Conditions ◽  
Magnetic Devices ◽  
Disordered Alloys ◽  
Ordered Intermetallic ◽  
Intermetallic Nanoparticles

<div> <p>The synthesis of alloys with long range atomic scale ordering (ordered intermetallics) is an emerging field of nanochemistry. Ordered intermetallic nanoparticles are useful for a wide variety of applications such as catalysis, superconductors, and magnetic devices. However, the preparation of nanostructured ordered intermetallics is challenging in comparison to disordered alloys, hindering progress in materials development. We report a process for converting colloidally synthesized ordered intermetallic PdBi<sub>2</sub> to ordered intermetallic Pd<sub>3</sub>Bi nanoparticles under ambient conditions by an electrochemically induced phase transition. The low melting point of PdBi<sub>2</sub> corresponds to low vacancy formation energies which enables the facile removal of the Bi from the surface, while simultaneously enabling interdiffusion of the constituent atoms via a vacancy diffusion mechanism under ambient conditions. The resulting phase-converted ordered intermetallic Pd<sub>3</sub>Bi exhibits 11x and 3.5x higher mass activty and high methanol tolerance for the oxygen reduction reaction compared to Pt/C and Pd/C, respectively,which is the highest reported for a Pd-based catalyst, to the best of our knowledge. These results establish a key development in the synthesis of noble metal rich ordered intermetallic phases with high catalytic activity, and sets forth guidelines for the design of ordered intermetallic compounds under ambient conditions.</p> </div>

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