کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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635777 | 1456104 | 2011 | 11 صفحه PDF | دانلود رایگان |

The objective of this work was to investigate the effect of polydimethylsiloxane (PDMS) molecular weights on the pervaporation performance and the confinement behavior of PDMS/ceramic composite membranes for the separation of ethanol from aqueous solutions by pervaporation. PDMS with three different molecular weights was used to prepare PDMS/ceramic composite membranes. Due to the fact that high molecular weight PDMS tends to suppress the formation of defects, and as a result improves the constrained degree of the membrane, the PDMS/ceramic composite membrane fabricated with the highest molecular weight PDMS exhibited a better performance than the other two counterparts prepared with lower molecular weight PDMS. The total flux and the separation factor of a PDMS/ceramic composite membrane with a thin defect-free PDMS layer of 5 μm were 1.6 kg/m2 h and 8.9, respectively, at 40 °C when 5 wt.% of ethanol was used in the feed solution. Furthermore, the ceramic support showed a unique advantage in constraining the swelling of the separation layer, when compared with the conventional polymer support, which significantly improved the membrane stability, especially for PDMS with high molecular weights.
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► A polymer/ceramic composite membrane consisting of a thin defect-free polydimethylsiloxane (PDMS) supported on a macro-porous ceramic support was achieved by using a one-step dip-coating method.
► The presence of ceramic support suppressed the swelling of the polymer separation layer, and as a result significantly improved membrane stability.
► The composite membrane fabricated with higher molecular weight PDMS showed a higher level of the constrained degree.
► The temperature dependence of the separation performance of the ceramic supported PDMS membrane was distinctively different from the polymer supported counterpart, due to the unique constrained characteristics.
Journal: Journal of Membrane Science - Volume 375, Issues 1–2, 15 June 2011, Pages 334–344