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Comparative study of PVA/SiO2 and PVA/SiO2/glutaraldehyde (GA) nanocomposite membranes prepared by single-step solution casting method

机译:单步溶液流延法制备PVA / SiO2和PVA / SiO2 /戊二醛(GA)纳米复合膜的比较研究

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摘要

We prepared poly(vinyl alcohol) (PVA)/SiO2 and PVA/SiO2/glutaraldehyde (GA) nanocomposite membranes in a single step using the solution casting method. The structure, morphology, and properties of these nanocomposite membranes were characterized by Raman spectroscopy, atomic force microscopy, small- and wide-angle X-ray scattering, thermogravimetric analysis, differential scanning calorimetry, and dynamic mechanical analysis (DMA). The influence of silica and GA loading on the meso-scale characteristics of the composite membranes was investigated. The results showed that silica deposited in the form of small nanoparticles (similar to 1 nm) in the PVA/SiO2 membranes, while bigger submicron particles (>25 nm) were formed in the PVA/SiO2/GA membranes. The water uptake of the PVA/SiO2 membranes increased with temperature, but the PVA/SiO2/GA membranes were completely dissolved above 50 degrees C. We can therefore conclude that the addition of GA deteriorated the properties of PVA/SiO2 membranes. The thermal stability of the PVA/SiO2 membranes increased with the increasing silica loading with a maximum char yield of 46 % for PVA/SiO2/4T. Even DMA profiles indicated a promising increase in E-R (rubbery modulus) from 6 MPa (PVA membrane) to 1015 MPa (PVA/SiO2/4T) at 250 degrees C, showing high mechanical strength of these membranes.
机译:我们使用溶液流延法一步一步制备了聚乙烯醇(PVA)/ SiO2和PVA / SiO2 /戊二醛(GA)纳米复合膜。这些纳米复合膜的结构,形态和性能通过拉曼光谱,原子力显微镜,小和广角X射线散射,热重分析,差示扫描量热法和动态力学分析(DMA)进行表征。研究了二氧化硅和GA负载量对复合膜介观尺度特性的影响。结果表明,二氧化硅以小纳米颗粒(约1 nm)的形式沉积在PVA / SiO2膜中,而较大的亚微米颗粒(> 25 nm)则形成在PVA / SiO2 / GA膜中。 PVA / SiO2膜的吸水量随温度增加而增加,但PVA / SiO2 / GA膜在50摄氏度以上完全溶解。因此,我们可以得出结论,GA的添加会降低PVA / SiO2膜的性能。 PVA / SiO2膜的热稳定性随二氧化硅载量的增加而增加,PVA / SiO2 / 4T的最大炭收率为46%。甚至DMA曲线也表明E-R(橡胶模量)在250摄氏度下从6 MPa(PVA膜)增加到1015 MPa(PVA / SiO2 / 4T),显示出很高的机械强度。

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