Controllable assembly, characterization and catalytic properties of a new Strandberg-type organophosphotungstate

2016 ◽  
Vol 45 (4) ◽  
pp. 1631-1637 ◽  
Author(s):  
Hong-Xin Ma ◽  
Jing Du ◽  
Zai-Ming Zhu ◽  
Ting Lu ◽  
Fang Su ◽  
...  

A new Strandberg-type organophosphotungstate was assembled under hydrothermal conditions and displayed good fluorescence properties and catalytic activity.

1979 ◽  
Vol 44 (4) ◽  
pp. 1015-1022 ◽  
Author(s):  
Viliam Múčka

The catalytic properties of two-component catalyst nickel oxide-cadmium oxide with the proportions of the components covering the whole composition region 0-100% were examined by studying the decomposition of hydrogen peroxide in aqueous solution on it. In the range 0-25 mol.% CdO, cadmium oxide is found to affect infavourably the ability of nickel oxide to chemisorb oxygen. The amount of the chemisorbed oxygen increases several times on gamma irradiation of the samples. The effect of cadmium oxide on the catalytic activity of the system shows up in fresh samples only indirectly via the changed amount of the oxygen chemisorbed. In older samples the initial catalytic activity of the system is changed, which can be explained based on the concept of bivalent catalytic centres in terms of the co-action of the catalytic centres of the two oxides, which are in equilibrium. The irradiation of the system under study speeds up the processes leading to the establishing of this equilibrium which is thermally very stable, and results in a substantial increase of the catalytic activity of the samples investigated.


1988 ◽  
Vol 53 (8) ◽  
pp. 1636-1646 ◽  
Author(s):  
Viliam Múčka ◽  
Kamil Lang

Some physical and catalytic properties of the two-component copper(II)oxide-chromium(III)oxide catalyst with different content of both components were studied using the decomposition of the aqueous solution of hydrogen peroxide as a testing reaction. It has been found that along to both basic components, the system under study contains also the spinel structure CuCr2O4, chromate washable by water and hexavalent ions of chromium unwashable by water. The soluble chromate is catalytically active. During the first period of the reaction the equilibrium is being established in both homogeneous and heterogeneous catalytic systems. The catalytic activity as well as the specific surface area of the washed solid is a non-monotonous function of its composition. It seems highly probable that the extreme values of both these quantities are not connected with the detected admixtures in the catalytic system. The system under study is very insensitive with regard to the applied doses of gamma radiation. Its catalytic properties are changed rather significantly after the thermal treatment and particularly after the partial reduction to low degree by hydrogen. The observed changes of the catalytic activity of the system under study are very probably in connection with the changes of the valence state of the catalytically active components of the catalyst.


Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 88
Author(s):  
Diana García-Pérez ◽  
Maria Consuelo Alvarez-Galvan ◽  
Jose M. Campos-Martin ◽  
Jose L. G. Fierro

Catalysts based on zirconia- and alumina-supported tungsten oxides (15 wt % W) with a small loading of platinum (0.3 wt % Pt) were selected to study the influence of the reduction temperature and the nature of the support on the hydroisomerization of n-dodecane. The reduction temperature has a major influence on metal dispersion, which impacts the catalytic activity. In addition, alumina and zirconia supports show different catalytic properties (mainly acid site strength and surface area), which play an important role in the conversion. The NH3-TPD profiles indicate that the acidity in alumina-based catalysts is clearly higher than that in their zirconia counterparts; this acidity can be attributed to a stronger interaction of the WOx species with alumina. The PtW/Al catalyst was found to exhibit the best catalytic performance for the hydroisomerization of n-dodecane based on its higher acidity, which was ascribed to its larger surface area relative to that of its zirconia counterparts. The selectivity for different hydrocarbons (C7–10, C11 and i-C12) was very similar for all the catalysts studied, with branched C12 hydrocarbons being the main products obtained (~80%). The temperature of 350 °C was clearly the best reduction temperature for all the catalysts studied in a trickled-bed-mode reactor.


Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4508
Author(s):  
Zeinab Mcheik ◽  
Ludovic Pinard ◽  
Joumana Toufaily ◽  
Tayssir Hamieh ◽  
T. Jean Daou

Hierarchical MOR-type zeolites were synthesized in the presence of hexadecyltrimethylammonium bromide (CTAB) as a porogen agent. XRD proved that the concentration of CTAB in the synthesis medium plays an essential role in forming pure hierarchical MOR-type material. Above a CTAB concentration of 0.04 mol·L−1, amorphous materials are observed. These hierarchical mordenite possess a higher porous volume compared to its counterpart conventional micrometer crystals. Nitrogen sorption showed the presence of mesoporosity for all mordenite samples synthesized in the presence of CTAB. The creation of mesopores due to the presence of CTAB in the synthesis medium does not occur at the expense of zeolite micropores. In addition, mesoporous volume and BET surface seem to increase upon the increase of CTAB concentration in the synthesis medium. The Si/Al ratio of the zeolite framework can be increased from 5.5 to 9.1 by halving the aluminum content present in the synthesis gel. These synthesized hierarchical MOR-type zeolites possess an improved catalytic activity for n-hexane cracking compared to large zeolite crystals obtained in the absence of CTAB.


2021 ◽  
Author(s):  
Chen-Lin Luo ◽  
Chu-Xing Hu ◽  
Ping Shang ◽  
Guan-Zhao Wen ◽  
Jia-Jun Zhu ◽  
...  

A series of heteroleptic Cu(i) complexes were precisely synthesized using different bipyridine and diphosphine ligands. These complexes exhibited fluorescence sensing towards silver ions and high catalytic activity towards the CuAAC reaction.


RSC Advances ◽  
2014 ◽  
Vol 4 (55) ◽  
pp. 28848-28851 ◽  
Author(s):  
Yanhui Zhang ◽  
Dongdi Zhang ◽  
Zhiyuan Huo ◽  
Pengtao Ma ◽  
Jingyang Niu ◽  
...  

The novel undecatungstoarsenate-supported carbonyl rhenium derivative exhibits prominent catalytic activity and high selectivity in the cycloaddition of epoxides.


1986 ◽  
Vol 51 (8) ◽  
pp. 1571-1578 ◽  
Author(s):  
Alois Motl

The radiation catalytic properties of the BASF K-3-10 catalyst were studied, namely the dependence of these effects on the time interval between the catalyst irradiation and the reaction itself and also on the length of the catalyst use. The catalytic effects decrease exponentially with the interval between the irradiation and the reaction if the catalyst is kept in the presence of air. The stability of effects induced by various types of radiations increases in the sequence beta radiation - gamma radiation - fast neutrons. The radiation catalytic effect stability in the reaction increases in the same sequence.


2012 ◽  
Vol 549 ◽  
pp. 733-736
Author(s):  
Xiao Mian Chen ◽  
Jing Jing Shi ◽  
Hong Sha Su ◽  
Chun Ting Lin ◽  
En Long Yang

The catalytic properties of nano-TiO2 modified fabric suits the demand for self-cleaning in recent years. In this paper, advanced and innovative technology were used to synthesize water sol of titanium dioxide photocatalyst with high catalytic activity for fabric finishing. The wear behavior, antibacterial property and water repellency of treated and untreated fabric were tested. Results indicate that finishing and washing of the titanium dioxide had no effect on wear behavior; finished and washed fabric has a certain antibacterial and water repellent properties.


2015 ◽  
Vol 3 (29) ◽  
pp. 15074-15081 ◽  
Author(s):  
Abhijit Biswas ◽  
Subir Paul ◽  
Arindam Banerjee

Peptide functionalized carbon nanodot supported Ru nanodots have been synthesized, which show a remarkable and reusable catalytic activity for the transformation of organic azide to the corresponding amine in the presence of other functional groups in water.


1995 ◽  
Vol 60 (6) ◽  
pp. 977-982
Author(s):  
S. Sugunan ◽  
V. Meera

The electron donor properties of perovskite-type mixed oxides (LaFeO3, PrFeO3, SmFeO3, LaCoO3, PrCoO3, SmCoO3, LaNiO3, PrNiO3 and SmNiO3) were studied based on the adsorption of electron acceptors exhibiting different electron affinity viz. 7,7,8,8-tetracyanoquinodimethane, 2,3,5,6-tetrachloro-1,4-benzoquinone, p-dinitrobenzene, and m-dinitrobenzene. The surface acidity/basicity of the oxides was determined using a set of Hammett indicators. The data were correlated with the catalytic activity of the oxides for the reduction of cyclohexanone with 2-propanol.


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