Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Payne Cell Gravimetric Measurements in Polymer-Solvent Systems for Diffusion Coefficients and Isotherm Data(Wiley, 2021) Zielinski, John M.; Garcia, Armando R.; Alsoy Altınkaya, SacideThe discussion focuses on the application of a Payne cell to the measurement of diffusion and solubility coefficients in polymer/solvent systems. Payne cells have, thus far, been used exclusively to measure steady-state permeation rates of solvents. An analytical model has been developed to describe transient gravimetric sorption and desorption measurements performed with a Payne cell. The model has been validated by a complementary numerical simulation and has been applied to evaluate diffusion and solubility coefficients in two different toluene-silicone rubber systems. The data measured using the Payne cell are found to compare very well with diffusion coefficient and isotherm data measured by traditional gravimetric sorption experiments.Article Citation - WoS: 1Citation - Scopus: 1The Effect of Mass Transfer Resistance and Nonuniform Initial Solvent Concentration on Permeation Through Polymer Membranes(John Wiley and Sons Inc., 2018) Zielinski, John M.; Alsoy Altınkaya, SacideA numerical simulation model has been developed which enables one to examine the effects of surface mass transfer resistance on the evaluation of permeation (P*), diffusion (D), and solubility (S) coefficients from unsteady-state mass transfer experiments as well as the transmission rate. A complementary analytical expression has been developed which validates the numerical model and facilitates the evaluation of the concentration dependence of P*, D, and S from sequential step-change experiments, under experimental conditions when the surface mass transfer resistance can be neglected.Article Citation - WoS: 6Citation - Scopus: 7Solubility and Diffusivity of Methylmethacrylate and Butylacrylate Monomers in a Mma-Ba Copolymer(John Wiley and Sons Inc., 2007) Yürekli, Yılmaz; Alsoy Altınkaya, Sacide; Zielinski, John M.Mutual diffusion coefficients and sorption isotherms of methyl methacrylate (MMA) and butyl acrylate (BA) monomers in methyl methacrylate-butyl acrylate copolymer (MMA-BA) have been measured by gravimetric sorption. MMA is found to have higher solubility and diffusion rates in the copolymer than BA. Sorption data for MMA were interpreted using classical Flory-Huggins thermodynamic theory with a constant interaction parameter (χ). A modified version of this theory has been applied to correlate the sorption data of BA, which exhibit a temperature and concentration-dependent χ parameter. For MMA, the isotherm data reveal enhanced polymer-solvent interactions with increasing temperature, while for BA the data indicate a drive toward phase separation with increasing temperature. Despite the difference in thermodynamic behavior, both monomers are found to exhibit Fickian diffusion and the diffusivity data are correlated reasonably well with the Vrentas-Duda free volume theory. Some deviation between the free-volume correlation and the experimental data is observed at the lowest temperature and BA concentration examined.Article Citation - WoS: 22Citation - Scopus: 22Onsager consistency checks for multicomponent diffusion models(John Wiley and Sons Inc., 2001) Zielinski, John M.; Alsoy Altınkaya, SacideThe Onsager reciprocity relations are applied to several recently proposed multicomponent diffusion models in an attempt to gauge their validity and ascertain their applicability. Each of these friction-based diffusion models stems from the more general Bearman formalism through various assumptions regarding the individual friction coefficients. By assessing the compliance of the Bearman model with respect to the Onsager relations, we ascertain the validity of the simplifications introduced to each diffusion model and suggest which postulates lead to results consistent with the Onsager relations. Although some models are not consistent with the Onsager relations, each model predicts the multicomponent drying of polymer films reasonably well. The necessity for consistency with the Onsager development is, therefore, revisited.