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For very thin materials, the surface area remains relatively constant when the material degrades, which allows surface erosion to be characterized as zero order release since the rate of degradation is constant. [2] [3] In bulk erosion, the erosion rate depends on the volume of the material. [3]
where A and B are reactants C is a product a, b, and c are stoichiometric coefficients,. the reaction rate is often found to have the form: = [] [] Here is the reaction rate constant that depends on temperature, and [A] and [B] are the molar concentrations of substances A and B in moles per unit volume of solution, assuming the reaction is taking place throughout the volume of the ...
is the rate constant for surface adsorption, m 3 ·mol −1 ·s −1 k − 1 {\displaystyle k_{-1}} is the rate constant for surface desorption, s −1 C S {\displaystyle C_{\mathrm {S} }} is highly related to the total surface area of the adsorbent: the greater the surface area, the more sites and the faster the reaction.
In physical chemistry, the Arrhenius equation is a formula for the temperature dependence of reaction rates.The equation was proposed by Svante Arrhenius in 1889, based on the work of Dutch chemist Jacobus Henricus van 't Hoff who had noted in 1884 that the van 't Hoff equation for the temperature dependence of equilibrium constants suggests such a formula for the rates of both forward and ...
The constant is the reaction rate constant or rate coefficient and at very few places velocity constant or specific rate of reaction. Its value may depend on conditions such as temperature, ionic strength, surface area of an adsorbent , or light irradiation .
Forced degradation or accelerated degradation is a process whereby the natural degradation rate of a product or material is increased by the application of an additional stress. Introduction [ edit ]
In consequence, the reaction rate constant increases rapidly with temperature , as shown in the direct plot of against . (Mathematically, at very high temperatures so that E a ≪ R T {\displaystyle E_{\text{a}}\ll RT} , k {\displaystyle k} would level off and approach A {\displaystyle A} as a limit, but this case does not occur under practical ...
L. M. Kachanov [5] and Y. N. Rabotnov [6] suggested the following evolution equations for the creep strain ε and a lumped damage state variable ω: ˙ = ˙ ˙ = ˙ where ˙ is the creep strain rate, ˙ is the creep-rate multiplier, is the applied stress, is the creep stress exponent of the material of interest, ˙ is the rate of damage accumulation, ˙ is the damage-rate multiplier, and is ...