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Effect of temperature - Arrhenius LawPosted by composite agency on October 14, 2004 at 17:10:03: D(T)=D0 e -[E / R x T] or S(T)=S0 e -[H / R x T] D(T) / S(T): diffusion coefficient / solubility as function of temperature [m2/s] / [gram / m3]. D0 / S0: the diffusion coefficient / solubility when the temperature goes to infinitity [m2/s] / [gram/m3]. E / H: the activation energy for diffusion / the mixture enthalpy [Joule/ mole]. R: Universal gas constant ( 8.314 Joule / Mole x Kelvin). T: Temperature (Kelvin).
Physical Considerations The temperature dependence of the diffusion coefficient (D) of, for example, carbon dioxide in high density polyethylene can be obtained by using the formula based on the Van 't Hoff Equation or Arrhenius Law. Realize that the temperature dependence of the solubility (S) of substance in materials is often also calculated by this Arrhenius Law. Moreover, as the steady state permeability (P), follows from D times S, the permeation rate also follows an Arrhenius type of temperature behaviour. Below we list some important consistencies with regard to the above: 1] From the general accepted picture of the mechanism of the activated diffusion process, it is known that larger holes need to be formed in the polymer for the diffusion of larger molecules. These will require a larger energy for their formation and hence the activation energy will be larger for the diffusion of bigger molecules, and the diffusivity will be smaller. 2] Hence, polymers and coatings with a small molecular free volume because with a high degree of crystallinity, will have a high activation energy for diffusion. 3] When passing the Glass Transition temperature heading for a higher temperature, the Activation Energy stays constant or increases. Concerning polymers that have a low free volume, such as partly crystalline polyamide (PA) or polyimide (PI), the change of activation energy is significant. For amorphous polymers, like polymethamethacrylate (PMMA) there is no change of activation energy. Whether the activation enery increases or decreases most probably depends on the degree of plasticizing by the permeant and the size of permeant relative to the free volume in the polymer. Read more on solubility of gases and liquids in polymers in the section of Hildebrand solubility parameters. Click here. 5] Effect of crosslinking 6] One may question what happens with permeability P as a function of temperature. In case of liquid and solvent permeation in polymer and composite materials this is obvious: permeability increases as a function of temperature. When dealing with a gas, usually the acitvation energy for diffusion is higher than the possible negative enthalpy of solution, hence the permeability also increases as a function of temperature. Example We measured the diffusivity of carbon dioxide in high density polyethylene with a crystalline fraction of 0.77, at a temperature of 40 and 50 degrees Celsius (313 and 323 Kelvin). We want to know the diffusion coefficient at 60 degrees Celsius.
D (313 Kelvin) = 4.0
E-11 m2/s 37 Kilo Joule (37 KJ).
Then the diffusion coefficient at 60 degrees Celsius is: Learn More Go to the plastics, elastomer, coatings and polymers and composite material properties forum to learn more on diffusion, chemical resistance and mechanical properties of polymers & composites. Interested in watching molecules actually diffusing through a substance? click here for the movie on Brownian Movement.
Compose your comments on composite agency with regard to Arrhenius law applied on solubility, diffusivity and permeability in polymer and composite materials.
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