نتایج جستجو برای: catalyst deactivation function

تعداد نتایج: 1260124  

2015
Khalid Hannan Andrew Canham

Various distillates are treated with hydrogen gas during hydrotreatment in the presence of catalyst in order to reduce the sulfur and aromatic content of the product. Optimal hydrotreater performance is essential for producing Nynas specialty oils, in order to fulfill the planned production volume and to meet the product specification. Loss of catalyst activity is inevitable during the producti...

2014
Giuseppe Trunfio

The deactivation pattern of a “model” Ni/MgO catalyst in the pre-reforming of n-hexane with steam (T, 450 °C; P, 5–15 bar) is reviewed. The influence of the steam-to-carbon ratio (S/C, 1.5–3.5) on the rate of catalyst fouling by coking is ascertained. Catalyst fouling leads to an exponential decay in activity, denoting 1-order dependence of the coking process on active sites availability. Hydro...

2012
Krasimir Ivanov Dimitar Dimitrov Boyan Boyanov

The paper relates to a catalyst, comprising copperchromium spinel, coated on carrier γ-Al2O3. The effect of preparation conditions on the active component composition and activity behavior of the catalysts is discussed. It was found that the activity of carbon monoxide, DME, formaldehyde and methanol oxidation reaches a maximum at an active component content of 20 – 30 wt. %. Temperature calcin...

1999
M. R. RAHIMPOUR

Frequently the activity of fresh catalyst changes with time in use. The decrease or increases of the catalyst activity with time during the course of reaction forces the system to an unsteady state operation ([1], [2], [3], [4] and [5]). One of these catalysts is the copper/zinc oxide catalyst, which is industrially used for methanol production. The activity of copper/zinc oxide catalyst declin...

2017
Noor Al-Rifai Peter J. Miedziak Moataz Morad Meenakshisundaram Sankar Conor Waldron Stefano Cattaneo Enhong Cao Samuel Pattisson David Morgan Donald Bethell Graham J. Hutchings Asterios Gavriilidis

Highly active, supported Au−Pd catalysts have been tested for catalyzing benzyl alcohol oxidation in a siliconglass micropacked bed reactor. The effects of Au−Pd composition and anion content during catalyst preparation on catalyst deactivation were studied, and a relationship between the deactivation rate and the amount of Cl− and Au used in the catalyst formulation was found. While Au aids in...

2007
Roberto Galiasso Tailleur

Diesel fuels of 50 and 15 ppm of sulfur content were produced in a pilot plant by upgrading light catalytic cracking gas oil (LCO) during 10 weeks of continuous operation. The end-of-run catalysts were characterized before and after soluble coke extraction by CH2Cl2. The cokes were characterized by CNMR, TPO, GC-MS, and elemental analysis. Catalyst surfaces were characterized by XPS, CO adsorpt...

Journal: :Journal of the American Chemical Society 2006
Neal K Devaraj Peter H Dinolfo Christopher E D Chidsey James P Collman

We demonstrate selective functionalization of independently addressed microelectrodes by electrochemical activation and deactivation of a coupling catalyst. 1,2,3-Triazole formation between terminal acetylenes and organic azides is efficiently catalyzed by copper(I) complexes (a Sharpless "click" reaction), while the oxidized copper(II) complexes are inactive. By electrochemically activating or...

2017
Jakob M. Christensen Peter A. Jensen Anker D. Jensen

Alkali-promoted cobalt molybdenum sulfide is a potential catalyst for the conversion of syngas into higher alcohols. This work is an investigation of how the feed composition influences the behavior of the sulfide catalyst. In a sulfur-free syngas the production of higher alcohols is observed to be optimal with an equimolar mixture of CO and H2 in the feed, while the methanol production benefit...

2015
Bin Dai Qinqin Wang Feng Yu Mingyuan Zhu

A detailed study of the valence state and distribution of the AuCl3/AC catalyst during the acetylene hydrochlorination deactivation process is described and discussed. Temperature-programmed reduction and X-ray photoelectron spectral analysis indicate that the active Au(3+) reduction to metallic Au(0) is one reason for the deactivation of AuCl3/AC catalyst. Transmission electron microscopy char...

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