2016
DOI: 10.1016/j.memsci.2016.03.054
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Kinetic and equilibrium sorption of organic liquids and vapors in Matrimid

Abstract: This work examines the sorption, diffusion, and polymer relaxation behavior for a variety of organic penetrants in Matrimid. The diffusionrelaxation model for plasticizing penetrants in glassy polymers developed by Berens and Hopfenberg appropriately captures the kinetic behavior of the organic vapor/polymer systems.

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Cited by 10 publications
(17 citation statements)
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References 68 publications
(93 reference statements)
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“…In further investigations, one may also consider the relative mobility of polymer chains as a function of temperature and the possible use of an additional vapor penetrant (i.e. one of the alcohols extensively studied in our previous work) to induce swelling of the polymer matrix and allow enhanced polymer chain motion. This approach may produce a greater degree of crosslinking as opposed to EDA exposure alone.…”
Section: Resultssupporting
confidence: 91%
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“…In further investigations, one may also consider the relative mobility of polymer chains as a function of temperature and the possible use of an additional vapor penetrant (i.e. one of the alcohols extensively studied in our previous work) to induce swelling of the polymer matrix and allow enhanced polymer chain motion. This approach may produce a greater degree of crosslinking as opposed to EDA exposure alone.…”
Section: Resultssupporting
confidence: 91%
“…Vapor sorption experiments were performed with Matrimid spin‐coated AT‐cut quartz crystals. The vapor sorption experimental setup is shown in Figure and the procedural details are explained in depth in our previous work . Unmodified and crosslinked Matrimid films were exposed to each 0.2 P / P sat increment for each penetrant for 48 h, except pentanol, which required 76 h to reach equilibrium.…”
Section: Methodsmentioning
confidence: 99%
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“…The conventional technique used to determine the concentration of drugs released of nanoparticles is by dialysis or centrifugation, and the drug concentration is then determined by UV‐spectrophotometry or high‐performance liquid chromatography . A better and more accurate method is the use of drug selective electrode (DSE), where large amounts of data can be acquired, making the fitting of nonlinear Berens and Hopfenberg kinetic model possible …”
Section: Introductionmentioning
confidence: 99%