Catalytic performance of Keplerate polyoxomolybdates in green epoxidation of alkenes with hydrogen peroxide

RSC Advances ◽  
2015 ◽  
Vol 5 (86) ◽  
pp. 70424-70428 ◽  
Author(s):  
Fariba Jalilian ◽  
Bahram Yadollahi ◽  
Mostafa Riahi Farsani ◽  
Shahram Tangestaninejad ◽  
Hadi Amiri Rudbari ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Catalytic Performance ◽  
Epoxidation Of Alkenes

The catalytic activity of three Keplerate POM, Mo72M30 (V, Cr and Fe), in the green epoxidation of alkenes with 30% H2O2 in water are investigated. Mo72Cr30 was shown the highest catalytic activity and efficiently reused without any loss of activity.

scholarly journals Properties and catalytic performance of sulphate-vanadia impregnated fumed silica as oxidative catalyst

2015 ◽  
Vol 11 (2) ◽  
Author(s):  
Nor Masdiana Zulkeple ◽  
Norhasyimah Mohd Kamal ◽  
Jamilah Mohd Ekhsan ◽  
Salasiah Che Me ◽  
Swee Ean Lim ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Charge Transfer ◽  
Surface Area ◽  
Sulphuric Acid ◽  
Fumed Silica ◽  
Catalytic Performance ◽  
Support Surface ◽  
High Catalytic Activity ◽  
Impregnation Method

A series of sulphate-vanadia impregnated fumed silica oxidative catalysts were synthesized via impregnation method. The samples were prepared by impregnation of 1 wt% of vanadium and 0.2 M of sulphuric acid onto fumed silica as support. Surface area of the silica supported samples were similar of 118 m2/g. UV-Vis DRS results showed existence of o supported V species and the charge transfer bands associated with O2- to V5+ in tetrahedral environments. Catalytic performance were evaluated via epoxidation of 1-octene to 1,2-epoxyoctane using hydrogen peroxide as an oxidant. It had been demonstrated that sulphate-vanadia impregnated fumed silica had high catalytic activity of 626 ± 0.2 mmol epoxide was produced after 24 h reaction. This may indicate that more oxidative sites were generated after the impregnation of V and sulphate onto the SiO2 matrixes.

Remediation of model wastewater polluted with methyl parathion by reverse micelle entrapped peroxidase

2011 ◽  
Vol 46 (4) ◽  
pp. 345-354
Author(s):  
Zoheb Karim ◽  
Qayyum Husain ◽  
Rohana Adnan ◽  
Naseem Akhtar
Keyword(s):  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Reverse Micelle ◽  
Oxidation Reaction ◽  
Methyl Parathion ◽  
Catalytic Performance ◽  
Redox Mediators ◽  
Ph Dependency ◽  
Effects Of Ph ◽  
Catalyzed Oxidation

The peroxidase/reverse micelle (RM) system effectively catalyzed the oxidation reaction in cyclohexane, while peroxidase from bitter gourd in aqueous buffer exhibited low catalytic activity. The oxidation of methyl parathion (MPT) has been optimized with effects of pH in the water pools, concentration of peroxidase and degree of surfactant hydration (Wo). The peroxidase/RM system showed a strong pH dependency. Its optimum catalytic activity was obtained when the peroxidase/RM was prepared in a buffer of pH 3.0. The effect of different redox mediators on the peroxidase-catalyzed oxidation of MPT was investigated. MPT was slowly oxidized by the peroxidase/RM system while the addition of phenol as a redox mediator strongly enhanced the catalytic performance of the peroxidase/RM system. Hydrogen peroxide strongly inhibited the activity of peroxidase; when the H2O2 was present at more than 0.80 mM, the MPT transformation was significantly reduced.

scholarly journals The Direct Synthesis of Hydrogen Peroxide over AuPd Nanoparticles: An Investigation into Metal Loading

2021 ◽  
Author(s):  
Joseph Brehm ◽  
Richard J. Lewis ◽  
David J. Morgan ◽  
Thomas E. Davies ◽  
Graham J. Hutchings
Keyword(s):  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Oxidation State ◽  
Direct Synthesis ◽  
Catalytic Performance ◽  
Metal Loading ◽  
Subsequent Degradation ◽  
Small Nanoparticles

AbstractThe direct synthesis of H2O2 from molecular H2 and O2 over AuPd catalysts, supported on TiO2 and prepared via an excess chloride co-impregnation procedure is investigated. The role of Au:Pd ratio on the catalytic activity towards H2O2 formation and its subsequent degradation is evaluated under conditions that have previously been found to be optimal for the formation of H2O2. The combination of relatively small nanoparticles, of mixed Pd-oxidation state is shown to correlate with enhanced catalytic performance. Subsequently, a detailed study of catalytic activity towards H2O2 synthesis as a function of AuPd loading was conducted, with a direct correlation between catalytic activity and metal loading observed. Graphic Abstract

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.

Decomposition of hydrogen peroxide on a two-component NiO-CdO catalyst and the effect of ionizing radiation on its catalytic properties

1979 ◽  
Vol 44 (4) ◽  
pp. 1015-1022 ◽  
Author(s):  
Viliam Múčka
Keyword(s):  
Aqueous Solution ◽  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Nickel Oxide ◽  
Catalytic Properties ◽  
Cadmium Oxide ◽  
Chemisorb Oxygen ◽  
Composition Region ◽  
Chemisorbed Oxygen ◽  
Two Component

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.

Hydrogen peroxide decomposition on a two-component CuO-Cr2O3 catalyst

1988 ◽  
Vol 53 (8) ◽  
pp. 1636-1646 ◽  
Author(s):  
Viliam Múčka ◽  
Kamil Lang
Keyword(s):  
Hydrogen Peroxide ◽  
Catalytic Activity ◽  
Extreme Values ◽  
Catalytic Properties ◽  
Active Components ◽  
Catalytic Systems ◽  
Heterogeneous Catalytic ◽  
Peroxide Decomposition ◽  
Two Component ◽  
Catalytically Active

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.

scholarly journals Influence of the Reduction Temperature and the Nature of the Support on the Performance of Zirconia and Alumina-Supported Pt Catalysts for n-Dodecane Hydroisomerization

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 88
Author(s):  
Diana García-Pérez ◽  
Maria Consuelo Alvarez-Galvan ◽  
Jose M. Campos-Martin ◽  
Jose L. G. Fierro
Keyword(s):  
Catalytic Activity ◽  
Surface Area ◽  
Catalytic Properties ◽  
Catalytic Performance ◽  
Major Influence ◽  
Pt Catalysts ◽  
Reduction Temperature ◽  
Metal Dispersion ◽  
Tungsten Oxides ◽  
Supported Pt Catalysts

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.

scholarly journals A diffusion anisotropy descriptor links morphology effects of H-ZSM-5 zeolites to their catalytic cracking performance

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Xiaoliang Liu ◽  
Jing Shi ◽  
Guang Yang ◽  
Jian Zhou ◽  
Chuanming Wang ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Catalytic Cracking ◽  
Catalytic Performance ◽  
Zeolite Catalysts ◽  
Time Resolved ◽  
Cracking Performance ◽  
Morphology Effect ◽  
Ft Ir ◽  
The Difference ◽  
Dynamics Simulations

AbstractZeolite morphology is crucial in determining their catalytic activity, selectivity and stability, but quantitative descriptors of such a morphology effect are challenging to define. Here we introduce a descriptor that accounts for the morphology effect in the catalytic performances of H-ZSM-5 zeolite for C4 olefin catalytic cracking. A series of H-ZSM-5 zeolites with similar sheet-like morphology but different c-axis lengths were synthesized. We found that the catalytic activity and stability is improved in samples with longer c-axis. Combining time-resolved in-situ FT-IR spectroscopy with molecular dynamics simulations, we show that the difference in catalytic performance can be attributed to the anisotropy of the intracrystalline diffusive propensity of the olefins in different channels. Our descriptor offers mechanistic insight for the design of highly effective zeolite catalysts for olefin cracking.

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