Title of article :
Studies on the pervaporation membrane of permeation water from methanol/water mixture
Author/Authors :
Xianhong Liu، نويسنده , , Yuan Sun، نويسنده , , Xinhua Deng، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
7
From page :
192
To page :
198
Abstract :
This investigation was performed to find if the nanometer SiO2 added in the membranes can improve the pervaperation performance of the membranes. Acrylic acid (AA) and acrylonitrile (AN) were synthesized by solution polymerization with and without nanometer SiO2. The copolymer solution was made into main body of the membranes, then composited with the polyvinyl alcohol (PVA) acetal membranes, to make the three-layer sandwich composite pervaporation membranes. The structure and the performance of the membranes were characterized by scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FT-IR), thermogravimetry (TG), dynamic themomechanical analysis apparatus (DMA) and mechanical property testing. Pervaporation experiments were carried out using these membranes to separate the mixtures of methanol/water over the complete concentration range 70–98%, and results showed that the selectivity of the membranes with nanometer SiO2 had notable improvement. For the 98% mixture at 60 °C, the separate factor is up to 1458, which is improved more than 10 times compared to the membranes without nanometer SiO2, the permeate flux is up to 325 g/(m2 h). For the 70% mixture at 70 °C, the separate factor arrived at 12, the permeate flux is up to 7097 g/(m2 h), which is improved more than 14 times compared to membranes without nanometer SiO2. It was concluded that the pervaperation performance of the membranes can improve greatly by nanometer SiO2.
Keywords :
Methanol/water mixture , Three-layer sandwich , Nanometer SiO2 , Pervaporation , Acrylic acid (AA)/acrylonitrile (AN) copolymer
Journal title :
Journal of Membrane Science
Serial Year :
2008
Journal title :
Journal of Membrane Science
Record number :
1354135
Link To Document :
بازگشت