نتایج جستجو برای: catalyst deactivation function

تعداد نتایج: 1260124  

Journal: Polyolefins Journal 2015

The olefins polymerization process in a slurry reactor is discussed. The reaction rate dynamics was analyzed and the contributions of feed flow, gas-liquid mass transfer, polymerization reaction, and catalyst deactivation were estimated. The propylene solubility in a solvent mixture “heptane” was calculated using Soave-Redlich-Kwong equation of state. These data were then approximated by Henry-...

2009
Xinli Zhu Trung Hoang Lance L. Lobban Richard G. Mallinson

Na promoted Pt/TiO2 catalysts have been studied under high severity, near equilibrium, conditions for use as a single stage WGS catalyst. Addition of 3 wt% Na to a 1 wt% Pt/TiO2 catalyst has been found to improve water gas shift activity significantly compared to Pt/TiO2, Pt/CeO2, and Pt–Re/TiO2 catalysts. This catalyst is stable when the reaction temperature is higher than 250 C. Deactivation ...

Journal: :Chemical communications 2012
Yingxu Wei Jinzhe Li Cuiyu Yuan Shutao Xu You Zhou Jingrun Chen Quanyi Wang Qing Zhang Zhongmin Liu

Formation of adamantane hydrocarbons and their confinement in SAPO-34 caused the long induction period and the quick catalyst deactivation in methanol conversion. Via ship-in-a-bottle synthesis, adamantane and methyladamantanes could be produced from methanol conversion in the cage of 8-ring SAPO catalysts under very mild reaction conditions.

Journal: :Chemical communications 2010
Héline Karaca Jingping Hong Pascal Fongarland Pascal Roussel Anne Griboval-Constant Maxime Lacroix Kai Hortmann Olga V Safonova Andrei Y Khodakov

The structure-activity relations in the alumina-supported cobalt catalysts are studied at the realistic conditions of Fischer-Tropsch synthesis using in situ time-resolved XRD and catalytic measurements. Cobalt sintering during the first 3-5 h of the reaction and cobalt carbidisation at a longer time on stream (>8 h) coincide with catalyst deactivation.

Journal: :Chemical science 2015
James J Devery Iii James J Douglas John D Nguyen Kevin P Cole Robert A Flowers Ii Corey R J Stephenson

Knowledge of the kinetic behavior of catalysts under synthetically relevant conditions is vital for the efficient use of compounds that mediate important transformations regardless of their composition or driving force. In particular, these data are of great importance to add perspective to the growing number of applications of photoactive transition metal complexes. Here we present kinetic, sy...

Journal: :Nanoscale 2013
Longfei Wu Hongbin Feng Mengjia Liu Kaixiang Zhang Jinghong Li

A facile and straightforward approach is developed for the construction of graphene-based hollow spheres. An electron rich sodium-ammonia solution is used to effectively restore the π-conjugation of graphene. The hollow spheres exhibit excellent electrocatalytic activity towards oxygen reduction without catalyst deactivation.

Journal: :Organic letters 2014
Kevin Lafaye Lionel Nicolas Amandine Guérinot Sébastien Reymond Janine Cossy

Cross-metathesis involving N-heteroaromatic olefinic derivatives is disclosed. The introduction of an appropriate substituent on the heteroaromatic ring decreases the Lewis basicity of the nitrogen atom, thus preventing the deactivation of the ruthenium-centered catalyst. The reaction is quite general in terms of both N-heterocycles and olefinic partners.

An empirical rate equation was obtained for the methanation kinetics catalyzed by MCR-2X, a commercial catalyst prepared by Haldor-Topsoe. The studies were carried out in a fixed-bed reactor under differential conditions, and in a gradientless recycle reactor (Berry) over a range of total pressures, reactant concentractions (H2/CO ratios), and temperatures. The kinetics of methanation were foun...

Abbas Ali Khodadadi Ahmad Tavasoli, Kambiz Sadaghiani Yadollah Mortazavi

In a novel dual bed reactor Fischer-Tropsch synthesis was studied by using two diffrent cobalt catalysts. An alkali-promoted cobalt catalyst was used in the first bed of a fixed-bed reactor followed by a Rutenuim promoted cobalt catalyst in the second bed. The activity, product selectivity and accelerated deactivation of the system were assessed and compared with a conventional single bed r...

Journal: :Sustainable Energy and Fuels 2022

The strong Brønsted and Lewis acid sites are active in the tandem conversion of levulinic into ethyl valerate. intrinsic activity former is more significant Pd/HBEA catalyst deactivation partially reversible by calcination.

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