ChemInform Abstract: STUDY OF PLATINUM-POLYAMIDE CATALYSTS, CATALYTIC BEHAVIOUR IN THE BENZENE HYDROGENATION REACTION

1973 ◽  
Vol 4 (41) ◽  
pp. no-no
Author(s):  
P. DINI ◽  
D. DONES ◽  
S. MONTELATICI ◽  
N. GIORDANO
2005 ◽  
Vol 228 (1-2) ◽  
pp. 319-324 ◽  
Author(s):  
Francisco Domínguez ◽  
Jorge Sánchez ◽  
Geomar Arteaga ◽  
Eduardo Choren

RSC Advances ◽  
2016 ◽  
Vol 6 (63) ◽  
pp. 58182-58187 ◽  
Author(s):  
Zhimin Xue ◽  
Weihong Chang ◽  
Yan Cheng ◽  
Jing Liu ◽  
Jian Li ◽  
...  

Porous poly(acrylamide)s nanoparticles prepared from CO2-in-PEG emulsions have high catalytic activity for benzene hydrogenation reaction.


2021 ◽  
Vol 340 ◽  
pp. 01026
Author(s):  
Sapar Konuspayev ◽  
Minavar Shaimardan ◽  
Nurlan Annas ◽  
T.S. Abildin ◽  
Y.Y. Suleimenov

Rhodium and rhodium-gold catalysts supported on amorphous aluminosilicates (ASA), titanium dioxide (rutile, TiO2) was prepared in two different ways: absorption and colloidal method. The catalysts were characterized by an inductively coupled plasma optical emission spectrometer (ICP-OES), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The activity and selectivity of the prepared catalysts were tested by the hydrogenation of benzene and toluene. Hydrogenation was conducted at a pressure of 4 MPa and a temperature 80 °C. The bimetallic Rh-Au/ASA catalyst prepared by the absorption method showed higher activity and selectivity in benzene hydrogenation reaction, the same catalyst prepared by the colloidal method demonstrated lower selectivity.


1998 ◽  
Vol 15 (2) ◽  
pp. 204-209
Author(s):  
N.M. da Fonseca ◽  
T.G.S. Neto ◽  
M.N.S.C. Roma ◽  
J. Felcman ◽  
D.S. Cunha ◽  
...  

Author(s):  
Congming Tang ◽  
Yue Zhao ◽  
Tao Li ◽  
Zhengjiang Liao ◽  
Benjing Xu ◽  
...  

Abstract Pd/CeO2 catalysts with different metallic Pd loading were synthesized by impregnation method. The physicochemical properties of prepared Pd/CeO2 catalysts and corresponding precursors were studied by XRD, XPS, H2-TPD and H2-TPR. Moreover, the catalytic performance of the Pd/CeO2 catalysts was investigated via gas phase benzene hydrogenation reaction at the temperature of 100–200 °C under atmosphere pressure. Results show that the catalytic performance of prepared Pd/CeO2 catalysts is directly related to the metallic Pd content. The amounts of active metallic Pd and adsorbed-desorbed hydrogen species on Pd/CeO2 catalysts increase with the increasing metallic Pd loading from 1.0 to 3.0%, while the numbers of them are slightly reduced on Pd/CeO2(3.5) catalyst. Furthermore, metallic Pd is highly dispersed on the nano-CeO2 supports, therefore, the prepared Pd/CeO2 catalysts present good gas phase benzene catalytic hydrogenation performance. At 200 °C, the benzene conversion over the Pd/CeO2 catalysts with different metallic Pd loading follows the rule: Pd/CeO2(3.0) > Pd/CeO2(3.5) > Pd/CeO2(2.5) > Pd/CeO2(2.0) > Pd/CeO2(1.5) > Pd/CeO2(1.0), corresponding values are 94.3, 96.4, 89.9, 82.8, 72.7, 42.6 and 94.3%. And the cyclohexane selectivity is 100% on all prepared Pd/CeO2 catalysts.


2020 ◽  
Author(s):  
hao yin ◽  
Liqing Zheng ◽  
Wei Fang ◽  
Yin-Hung Lai ◽  
Nikolaus Porenta ◽  
...  

<p>Understanding the mechanism of catalytic hydrogenation at the local environment requires chemical and topographic information involving catalytic sites, active hydrogen species and their spatial distribution. Here, tip-enhanced Raman spectroscopy (TERS) was employed to study the catalytic hydrogenation of chloro-nitrobenzenethiol on a well-defined Pd(sub-monolayer)/Au(111) bimetallic catalyst (<i>p</i><sub>H2</sub>=1.5 bar, 298 K), where the surface topography and chemical fingerprint information were simultaneously mapped with nanoscale resolution (≈10 nm). TERS imaging of the surface after catalytic hydrogenation confirms that the reaction occurs beyond the location of Pd sites. The results demonstrate that hydrogen spillover accelerates hydrogenation at the Au sites within 20 nm from the bimetallic Pd/Au boundary. Density functional theory was used to elucidate the thermodynamics of interfacial hydrogen transfer. We demonstrate that TERS as a powerful analytical tool provides a unique approach to spatially investigate the local structure-reactivity relationship in catalysis.</p>


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