A theoretical model is discussed to analyze the growth kinetics of gas bubbles in isothermal viscous polymer solutions. This model obtained by grafting the Tri Diagonal Matrix Algorithm (Patankar, Ref. [1]) into the cell model (Amon and Denson, Ref. [2]), eliminates many of the assumptions introduced in the previously reported mathematical models. Neglect of the convection term in the transient diffusion equation results in significant error in the prediction of the bubble growth. Assumption that diffusion of volatile solute is confined within a thin layer around the gas-liquid interface is also proved to be unrealistic when diffusion coefficient is relatively high. Physical parameters for expansion of nitrogen bubbles in vinylidene chloride-acrylonitrile copolymer at 100° (Barlow and Langlois, Ref. [3]) are taken to investigate the applicability of the model. Effect of initial bubble size on the growth behavior lasts a long time. Increase of diffusion coefficient and decrease of external pressure and viscosity of polymer solution enhance greatly the rate of bubble growth, whereas surface tension affects it only slightly.
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