Catalytic activity of rhodium(I) complexes containing poly(siloxy)alkyldiphenylphosphines

1980 ◽  
Vol 45 (7) ◽  
pp. 2100-2107 ◽  
Author(s):  
Vladimír Kavan ◽  
Martin Čapka
Keyword(s):  
Catalytic Activity ◽  
Hydrogen Pressure ◽  
Catalyst Activity ◽  
Molar Ratio ◽  
Normal Hydrogen ◽  
Kinetics Of

Kinetics of homogenous hydrogenation of 1-heptene catalysed by rhodium(I) complexes prepared in situ from di-μ.μ'-chloro-bis(dicyclooctenerhodium) and phosphine L (L = 2-(diethoxymethylsilyl)ethyldiphenylphosphine, 3-(diethoxymethylsilyl)propyldiphenylphosphine and their copolymers with diethoxydimethylsilane) have been studied at 64°C under normal hydrogen pressure. The dependence of the catalyst activity on the type of L( monomeric, polymeric, supported on silica) has been examined. The effects of Rh : P molar ratio, the concentration of phosphine groups in siloxane copolymers and of the method of catalyst fixation to support on catalyst performance are discussed.

Catalytic activity of rhodium(I) complexes containing (ω-trimethylsilylalkyl)diphenylphosphines

1980 ◽  
Vol 45 (8) ◽  
pp. 2219-2223 ◽  
Author(s):  
Marie Jakoubková ◽  
Martin Čapka
Keyword(s):  
Catalytic Activity ◽  
Nmr Spectroscopy ◽  
Ir Spectroscopy ◽  
Electron Density ◽  
Phosphorus Atom ◽  
Proton Acceptor ◽  
Trimethylsilyl Group ◽  
Kinetics Of

Kinetics of homogenous hydrogenation of 1-heptene catalysed by rhodium(I) complexes prepared in situ from μ,μ'-dichloro-bis(cyclooctenerhodium) and phosphines of the type RP(C6H5)2 (R = -CH3, -(CH2)nSi(CH3)3; n = 1-4) have been studied. The substitution of the ligands by the trimethylsilyl group was found to increase significantly the catalytic activity of the complexes. The results are discussed in relation to the electron density on the phosphorus atom determined by 31P NMR spectroscopy and to its proton acceptor ability determined by IR spectroscopy.

Time resolved growth of membrane stabilized silver NPs and their catalytic activity

RSC Advances ◽  
2014 ◽  
Vol 4 (103) ◽  
pp. 59379-59386 ◽  
Author(s):  
Sabyasachi Patra ◽  
Debasis Sen ◽  
Ashok K. Pandey ◽  
J. Bahadur ◽  
S. Mazumder ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Catalytic Activity ◽  
Growth Kinetics ◽  
Nanocomposite Membranes ◽  
Time Resolved ◽  
Catalytic Application ◽  
Silver Nps ◽  
First Time ◽  
Kinetics Of

Growth kinetics of membrane stabilized silver nanoparticles have been studied for the first time with time resolved in situ SAXS. The catalytic application of nanocomposite membranes thus formed has also been explored.

Nickel and cobalt phosphides as effective catalysts for oxygen removal of dibenzofuran: role of contact time, hydrogen pressure and hydrogen/feed molar ratio

2015 ◽  
Vol 5 (6) ◽  
pp. 3403-3415 ◽  
Author(s):  
A. Infantes-Molina ◽  
E. Gralberg ◽  
J. A. Cecilia ◽  
Elisabetta Finocchio ◽  
E. Rodríguez-Castellón
Keyword(s):  
Catalytic Activity ◽  
Contact Time ◽  
Hydrogen Pressure ◽  
Oxygen Removal ◽  
Molar Ratio ◽  
Metal Loading ◽  
Molar Ratios ◽  
Feed Molar Ratio

The catalytic activity of nickel and cobalt phosphides, with a metal loading of 5 wt.%, supported on silica was investigated in the hydrodeoxygenation reaction (HDO) of dibenzofuran (DBF) as a model oxygenated compound at different contact times, H2 pressures and H2/DBF molar ratios.

Oxidative Degradation and Kinetics of Trichloroethylene by Thermally Activated Persulfate

2014 ◽  
Vol 675-677 ◽  
pp. 547-550
Author(s):  
Jun Jie Yue ◽  
Xiao Qiao Zhu ◽  
Yu Ting Wang ◽  
Yu Qin Zhang ◽  
Li Zhao ◽  
...  
Keyword(s):  
Oxidative Degradation ◽  
Chemical Oxidation ◽  
Molar Ratio ◽  
Pseudo First Order Reaction ◽  
In Situ Chemical Oxidation ◽  
First Order ◽  
Molar Ratios ◽  
Thermally Activated ◽  
Kinetics Of

In situ chemical oxidation with persulfate (PS) anion (S2O82-) is a viable technique for remediation of groundwater contaminants such as trichloroethylene (TCE). This laboratory study investigated the use of the oxidant sodium PS for the chemical oxidation of TCE at different conditions to determine the influence of temperature, pH, and the PS/TCE molar ratio. Experiments revealed that higher temperatures, lower pH, and higher PS/TCE molar ratios were to the benefit of TCE oxidation by PS. By investigating the reaction kinetics, the degradations of contaminant can be described by use of pseudo-first-order reaction. At the temperatures ranging from 25°C to 40°C, the activation energy for the degradation of TCE was determined to be 85.04 KJ/mol.

Preparation of MnOx/CNTs Catalyst by in-Situ Precipitation Method For Low-Temperature NO Reduction with NH3

2020 ◽  
Vol 16 ◽  
Author(s):  
Yanbing Zhang ◽  
Yingzan Chen ◽  
Jinhe Huang ◽  
Mingjie Ding ◽  
Xiaoyan Li ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Low Temperature ◽  
Sodium Carbonate ◽  
Catalytic Reduction ◽  
Precipitation Method ◽  
Molar Ratio ◽  
Surface Element ◽  
Manganese Acetate ◽  
Nh3 Scr

Background: V2O5–WO3(MoO3)/TiO2 catalyst, as the core of selective catalytic reduction of NO with NH3 (SCR) has some drawbacks, such as high working temperature window (300-400oC), the toxicity of V-based catalyst and so on. Therefore, development of the catalyst with better low temperature denitration catalyst and weaker toxicity is necessary. Objective: Highly dispersed MnOx/CNTs catalysts with excellent denitration activity at 80-180oC, and weaker toxicity of MnOx. It is worth noting that an in-situ precipitation method based on the reaction of manganese acetate and sodium carbonate, which is advantageous to the in-situ deposition of active component, and the catalytic activity. Methods: MnOx/CNTs catalysts with different Mn/C molar ratio were fabricated by in-situ precipitation method due to the reaction of manganese acetate and sodium carbonate. And the microstructure, crystalline property, the content of surface element, valence state, redox property, and catalytic activity was confirmed by FESEM, TEM, XRD, XPS, TPD, and fixedbed reactor. Results: The as-prepared MnOx/CNTs catalysts exhibit outstanding low temperature SCR activity. And the NO conversion of the optimum 1.2% MnOx/CNTs catalyst reached 57.4-89.2% at 80-180oC, which resulted from the amorphous MnOx catalysts, higher ratio of Mn4+/Mn3+ and OS/(OS+OL). Conclusion: MnOx/CNTs catalysts have been prepared by the in-situ precipitation method based on the reaction of manganese acetate and sodium carbonate. And the resultant MnOx/CNTs catalysts presented excellent low temperature denitration activity between 80oC and 180oC. Among them, the 1.2% MnOx/CNTs catalyst exhibited the first rate low temperature denitration activity, and the denitration activity attained 57.4-89.2%, which may be owing to the presence of the weakly crystalline or amorphous MnOx, higher ratio of Mn4+/Mn3+ and OS/(OS+OL).

scholarly journals Zr-SBA-15 Lewis Acid Catalyst: Activity in Meerwein Ponndorf Verley Reduction

Catalysts ◽  
2015 ◽  
Vol 5 (4) ◽  
pp. 1911-1927 ◽  
Author(s):  
Jose Iglesias ◽  
Juan Melero ◽  
Gabriel Morales ◽  
Jovita Moreno ◽  
Yolanda Segura ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Lewis Acid ◽  
Reaction Temperature ◽  
Catalyst Activity ◽  
Acid Catalyst ◽  
Positive Influence ◽  
Molar Ratio ◽  
Special Focus ◽  
Molar Ratios ◽  
Lewis Acid Catalyst

Zr-SBA-15 Lewis acid catalyst has demonstrated an outstanding catalytic activity in the reduction of several carbonyl compounds by means of Meerwein Ponndorf Verley (MPV) reaction, using several secondary alcohols, and showing a very high selectivity towards the desired products. Special focus was addressed in the catalytic activity of Zr-SBA-15 material in the production of furfuryl alcohol from furfural, which is an important reaction for the lignocellulosic biomass valorization. In this transformation, both the reaction temperature and the i-PrOH:Furfural molar ratio exert a positive influence on the rate of the MPV transformation, with the influence of the former being much higher. i-propyl-furfuryl ether, a by-product resulting from the etherification of the target product with the sacrificing alcohol, is also found together with the main product. The production of this side-product is highly influenced by the reaction temperature, so that low temperatures and high sacrificing alcohol to substrate molar ratios have to be applied to keep its production at low levels.

scholarly journals Study of the Catalytic Activity of the Compounds Hydrotalcite Type Treated by Microwave in the Self-Condensation of Acetone

2021 ◽  
Vol 2021 ◽  
pp. 1-7
Author(s):  
Jamal Houssaini ◽  
Mohammed Naciri Bennani ◽  
Hamid Ziyat ◽  
Said Arhzaf ◽  
O. Qabaqous ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Condensation Reaction ◽  
Catalyst Activity ◽  
The Self ◽  
Conventional Heating ◽  
Molar Ratio ◽  
High Catalytic Activity ◽  
Adsorption Method ◽  
X Ray ◽  
Diacetone Alcohol

The self-condensation reaction of acetone, producing diacetone alcohol (DAA), is of great industrial importance. It was used to study the catalytic activity of Mg-Al catalysts synthesized by the coprecipitation method. For this purpose, we synthesized Mg-Al based hydrotalcite with a molar ratio of 3, obtained either after conventional heating or after microwave irradiation with of 100 W for three minutes. Structural and chemical properties of the obtained catalysts were characterized, using different techniques: X-ray diffraction (XRD), Fourier transform infrared spectra (FTIR), scanning electron microscope (SEM), equipped with energy dispersive X-ray (EDX), and specific surface area of the catalysts were determined by the methylene blue (MB) adsorption method. Also, these catalysts were tested in the self-condensation reaction of acetone at 273 K in the liquid phase without solvent, a reaction which requires very high catalytic activity. The microwave treatment improves the catalyst activity, and the conversion of acetone to diacetone alcohol increases from 13.2 to 18.3% after 8 h of reaction. Moreover, the microwave-treated hydrotalcite catalyst, calcined at 723 K and rehydrated under a flow of N2, is the most active and gives conversion of acetone of 52% under the same reaction conditions.

A Novel Gold Nanoparticle/Poly(AMPS-co-HEMA) Composite Hydrogel for Selective Catalysis

2011 ◽  
Vol 399-401 ◽  
pp. 704-707 ◽  
Author(s):  
Ke Ping Wang ◽  
Song Bai Lin ◽  
Na Na Wang ◽  
Ai Ru Ke
Keyword(s):  
Catalytic Activity ◽  
Reduction Reaction ◽  
Hydrogenation Rate ◽  
Processing Stage ◽  
Composite Gel ◽  
Growth Method ◽  
Selective Catalysis ◽  
Kinetics Of ◽  
Controllable Preparation

A modified seed-mediated growth method was developed for in situ controllable preparation of gold nanoparticles (GNPs) within P(AMPS-co-HEMA) hydrogel networks. When the time of cycles absorbing procedure increased in mother solutions under given temperature during the processing stage, the number of GNPs was significantly increased and networks were utilized for in situ nanoparticles synthesis by reduction of glod ion absorbed. TEM images confirmed that GNPs were between 100 and 200 nm in size and distributed uniformly in gel. The network embedded GNPs also endows the composite gel with selective catalytic activity for selective catalysis in the reduction of nitro compound (2-NP, 3-NP and 4-NP). The kinetics of the reduction reaction were investigated under the same condition, the result showed the GNPs gel system was found to have an excellent catalytic activity and high conversion for 4-NP reduction among nitrophenol homologue, the nitrophenol hydrogenation rate got to 6.63 mol/g min for reducing of 4-NP compared to 3.69 mol/g min, the rate of 2-NP. It was almost zero for 3-NP implying no catalytic activity, even though they were isomeride.

scholarly journals Improving the Performance of Gd Addition on Catalytic Activity and SO2 Resistance over MnOx/ZSM-5 Catalysts for Low-Temperature NH3-SCR

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 324
Author(s):  
Jinkun Guan ◽  
Lusha Zhou ◽  
Weiquan Li ◽  
Die Hu ◽  
Jie Wen ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Low Temperature ◽  
Photoelectron Spectroscopy ◽  
Active Sites ◽  
Molar Ratio ◽  
Manganese Sulfate ◽  
Nh3 Scr ◽  
So2 Resistance ◽  
Temperature Programmed

SO2 poisoning is a great challenge for the practical application of Mn-based catalysts in low-temperature selective catalytic reduction (SCR) reactions of NOx with NH3. A series of Gadolinium (Gd)-modified MnOx/ZSM-5 catalysts were synthesized via a citric acid–ethanol dispersion method and evaluated by low-temperature NH3-SCR. Among them, the GdMn/Z-0.3 catalyst with the molar ratio of Gd/Mn of 0.3 presented the highest catalytic activity, in which a 100% NO conversion could be obtained in the temperature range of 120–240 °C. Furthermore, GdMn/Z-0.3 exhibited good SO2 resistance compared with Mn/Z in the presence of 100 ppm SO2. The results of Brunauer–Emmett–Teller (BET), X-ray photoelectron spectroscopy (XPS), temperature-programmed reduction of H2 (H2-TPR) and temperature-programmed desorption of NH3 (NH3-TPD) illustrated that such catalytic performance was mainly caused by large surface area, abundant Mn4+ and surface chemisorbed oxygen species, strong reducibility and the suitable acidity of the catalyst. The in situ diffuse reflectance infrared Fourier transform spectra (DRIFTS) results revealed that the addition of Gd greatly inhibited the reaction between the SO2 and MnOx active sites to form bulk manganese sulfate, thus contributing to high SO2 resistance. Moreover, in situ DRIFTS experiments also shed light on the mechanism of low-temperature SCR reactions over Mn/Z and GdMn/Z-0.3, which both followed the Langmuir–Hinshelwood (L–H) and Eley–Rideal (E–R) mechanism.

In situ study of electron beam-induced chemical vapor deposition of Au in an environmental TEM

1995 ◽  
Vol 53 ◽  
pp. 256-257
Author(s):  
J. Drucker ◽  
R. Sharma ◽  
J. Kouvetakis ◽  
K.H.J. Weiss
Keyword(s):  
Electron Beam ◽  
Chemical Vapor Deposition ◽  
Vapor Deposition ◽  
Quantum Effect ◽  
Line Drawing ◽  
Chemical Vapor ◽  
Environmental Cell ◽  
Engineering Changes ◽  
Kinetics Of

Patterning of metals is a key element in the fabrication of integrated microelectronics. For circuit repair and engineering changes constructive lithography, writing techniques, based on electron, ion or photon beam-induced decomposition of precursor molecule and its deposition on top of a structure have gained wide acceptance Recently, scanning probe techniques have been used for line drawing and wire growth of W on a silicon substrate for quantum effect devices. The kinetics of electron beam induced W deposition from WF6 gas has been studied by adsorbing the gas on SiO2 surface and measuring the growth in a TEM for various exposure times. Our environmental cell allows us to control not only electron exposure time but also the gas pressure flow and the temperature. We have studied the growth kinetics of Au Chemical vapor deposition (CVD), in situ, at different temperatures with/without the electron beam on highly clean Si surfaces in an environmental cell fitted inside a TEM column.

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