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Degradation equation

Estimate the concentration of a discharged chemical at the intake point by 1) simple dilution, or by a simplified degradation equation with dilution. [Pg.371]

Several other polypyridyl metal complexes have been proposed as electrocatalysts for C02 reduction.100-108 For some of them HCOO- appears as the dominant product of reduction. It has been shown for instance that the complexes [Rhin(bpy)2Cl2]+ or [Rh n(bpy)2(CF3S03)2]+ catalyze the formation of HCOO- in MeCN (at —1.55 V vs. SCE) with a current efficiency of up to 80%.100,103 The electrocatalytic process occurs via the initially electrogenerated species [RhI(bpy)2]+, formed by two-electron reduction of the metal center, which is then reduced twice more (Rlr/Rn Rh°/Rh q. The source of protons is apparently the supporting electrolyte cation, Bu4N+ via the Hoffmann degradation (Equation (34)). [Pg.481]

Steady-State operation of a stripping tower with first-order degradation, equation (E6.5.7) gives... [Pg.155]

Some kinetic models for thermal or catalytic polymer degradation have been proposed. The commonly used approach is first-order kinetics to investigate the characteristics of degradation (Equation 9.1). In this approach at first the weight loss curve of polymers during the decomposition is determined, and overall rate constants are calculated... [Pg.226]

The conversion of a-hydroxy acids into aldehydes with one less carbon has great importance in the chemistry of sugars. Oxidation with bromine water transforms aldoses into the corresponding aldonic acids, which, in the form of their calcium salts, are treated with aqueous hydrogen peroxide in the presence of ferrous or ferric sulfate (Fenton reagent) and are degraded to aldoses with one less carbon (Ruff degradation) (equation 479) [57]. [Pg.228]

This leads to a consideration of reactions in which oi anosilicates are synthesized and degraded. Equations (3)—(5) describe theoretical reactions by which organosilicon esters or ethers may be formed in biological systems. [Pg.434]

L. fil. was determined by X-my analysis of its methiodide. It is thus a close relative of hetisine. The interesting chemical features were its pX (see Section 2B), its acetylation to an N-acetyl ketone and a basic 0-acetate, and its reaction with methyl iodide. The first stage in attempted Hofmann degradation (equation 3) gave the A-methyl ketone. Further methylation and treatment with silver... [Pg.348]

The existence of four independent degradation mechanisms prompts the formulation of a degradation equation". The incremental degradation dD, of a plastic due to the action of microbes B, macro-organisms M, photons P, and chemical C, behaves as follows ... [Pg.140]

Where a is the ECM protein degradation coefficient [5, 6]. In the simulations, this reaction occurred uniformly throughout the extracellular space. After solving for Cecm at each time step, it was used in the receptor-ligand kinetic equation to determine Cb. Note thatCb was also at steady-state at each time step because the time constant of the receptor-ligand system was much smaller than that for the ECM protein degradation equation. [Pg.429]


See other pages where Degradation equation is mentioned: [Pg.116]    [Pg.216]    [Pg.213]    [Pg.610]    [Pg.37]    [Pg.444]    [Pg.444]    [Pg.444]    [Pg.445]    [Pg.437]    [Pg.215]    [Pg.208]    [Pg.140]    [Pg.140]    [Pg.92]    [Pg.971]    [Pg.1399]    [Pg.550]   


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