نتایج جستجو برای: equation of deactivation rate

تعداد نتایج: 21218016  

2001
Dmitri A. Bulushev Sergei I. Reshetnikov Lioubov Kiwi-Minsker Albert Renken

Deactivation kinetics of a V/Ti-oxide catalyst was studied in partial oxidation of toluene to benzaldehyde (BA) and benzoic acid (BAc) at 523–573 K. The catalyst consisted of 0.37 monolayer of VOx species and after oxidative pre-treatment contained isolated monomeric and polymeric metavanadate-like vanadia species under dehydrated conditions as was shown by FT Raman spectroscopy. Under the reac...

Journal: :The Biochemical journal 1982
M N Jones P Manley A Wilkinson

1. The enzymic activity of glucose oxidase was determined as a function of pH and sodium n-dodecyl sulphate (SDS) concentration. 2. Glucose oxidase is not deactivated by SDS at pH 6 even after prolonged incubation, but is deactivated at pH 4.3 and 3.65. 3. Sedimentation-rate analysis showed that glucose oxidase dissociates into its two subunits at pH 5 and below, and sedimentation-equilibrium e...

Journal: :Biotechnology and bioengineering 2007
Mikkel Nordkvist Per Munk Nielsen John Villadsen

Oxidation of lactose to lactobionic acid by a Microdochium nivale carbohydrate oxidase was studied. The K(m)-value for lactose, obtained by a traditional enzymatic assay, was 0.066 mM at pH 6.4 and 38 degrees C. The effect of oxygen on the enzymatic rate of reaction as well as the operational stability of the enzyme was studied by performing reactions at constant pH and temperature in a stirred...

Journal: :Hypertension 1998
K Narkiewicz C A Pesek M Kato B G Phillips D E Davison V K Somers

-Patients with obstructive sleep apnea are at increased risk for hypertension. The mechanisms underlying this increased risk are not known. We tested the hypothesis that obstructive sleep apnea, independent of factors such as hypertension, obesity, and age, is characterized by impairment of baroreflex sensitivity. We measured muscle sympathetic nerve activity (MSNA) and heart rate responses to ...

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...

Journal: :journal of mining and environment 2016
h. dehghani n. mikhak beiranvand

one of the most important parameters used for determining the performance of tunnel boring machines (tbms) is their penetration rate. the parameters affecting the penetration rate can be divided in two categories. the first category is the controllable parameters such as the tbm technical characteristics, and type and geometry of the tunnel, and the second one is the uncontrollable parameters s...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2013
Yuzheng Hu Xi Chen Hong Gu Yihong Yang

Deactivation of the human brain's default mode network (DMN) is regarded as suppression of endogenous activity to support exogenous task-related processes. This phenomenon has important functional relevance and insufficient DMN deactivation has been implicated in several neuropsychiatric disorders. However, the neurochemical mechanism of the DMN's deactivation remains largely unknown. In the pr...

In this work, kinetics and thermodynamics of esterification reaction were studied. This research investigated the esterification reaction between methanol and acidified oil catalyzed by sulfonated cation exchange resin and proposed a new rate equation for consideration of kinetics of this reaction according to the Langmuir-Hinshelwood mechanism. Thermodynamics and kinetics parameters were calcu...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2010
Owen P Gross Marie E Burns

In rod photoreceptors, deactivation of the light-activated G-protein-coupled receptor rhodopsin (R*) is initiated by phosphorylation and completed through subsequent binding of visual arrestin (Arr1). The in vivo kinetics of these individual interactions have proven difficult to determine with precision since R* lifetime is much shorter than the lifetimes of downstream G-protein and effector mo...

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