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Preparation and characterization of PVDF microporous membrane with highly hydrophobic surface

机译:表面高疏水性PVDF微孔膜的制备与表征

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Using the mixture of triethyl phosphate (TEP) and N,N-dimethylacetamide (DMAc) as solvent, PVDF microporous membranes with highly hydrophobic surface were prepared by a modified NIPS method with a dual coagulation process. The effects of the exposure time on these membranes before being immersed into the coagulation bath and the composition in the coagulation bath on precipitation rate, membrane morphology, membrane hydrophobicity, membrane mechanical property, and membrane performance were studied. The morphologies and hydrophobicities of PVDF microporous membranes were investigated by scanning electron microscopy (SEM) and contact angle (CA) measurement. The precipitation processes were observed by light transmittance measurement. The pore size distribution was determined by liquid permeation technique. PVDF microporous membrane obtained by passing evaporation period of 60 min before being immersed into the water bath showed a high water CA of 122.1°. Using ethanol (EtOH) as coagulation bath, the water CAs of the top surface and bottom surface of the membrane increased to 125.9 and 132.6°, respectively. To further improve PVDF membrane hydrophobicity, a dual coagulation process was used and the mixed solvent (TEP-DMAc) was added into the first coagulation bath for 30 sec. Increase in the TEP-DMAc content led to the change in the morphology type of the membrane, that is, from an asymmetric structure with a dense top surface to a symmetric structure with a skinless top surface, and the pore size distribution widened greatly. By increasing the mass ratio of TEP to DMAc, the denseness of the membrane surface decreased significantly. Adding 60 wt% of TEP-DMAc to the first coagulation bath and the mass ratio of TEP to DMAc was 60:40, the CA reached to a maximum as high as 136.6°, and PVDF microporous membrane showed a high porosity of 80% and an excellent mechanical property of 3.14 MPa tensile strength and 61.79% elongation ratio.
机译:以磷酸三乙酯(TEP)和N,N-二甲基乙酰胺(DMAc)的混合物为溶剂,通过改进的NIPS方法,采用双重凝固工艺制备了具有高疏水性表面的PVDF微孔膜。研究了浸入时间对浸没在凝固浴中的这些膜和凝固浴中的组成的影响,对沉淀速率,膜形态,膜疏水性,膜机械性能和膜性能都有影响。通过扫描电子显微镜(SEM)和接触角(CA)测量研究了PVDF微孔膜的形貌和疏水性。通过透光率测量观察沉淀过程。孔径分布通过液体渗透技术确定。通过在浸入水浴之前经过60分钟的蒸发时间而获得的PVDF微孔膜显示出122.1°的高水CA。使用乙醇(EtOH)作为混凝浴,膜顶表面和底表面的水CAs分别增加至125.9和132.6°。为了进一步提高PVDF膜的疏水性,使用了双重凝结工艺,并将混合溶剂(TEP-DMAc)添加到第一凝结浴中30秒钟。 TEP-DMAc含量的增加导致膜的形态类型改变,即,从具有密集的顶表面的不对称结构变为具有无皮的顶部表面的对称结构,并且孔径分布大大变宽。通过增加TEP与DMAc的质量比,膜表面的密度显着降低。向第一凝结浴中添加60 wt%的TEP-DMAc,TEP与DMAc的质量比为60:40,CA最高可达136.6°,PVDF微孔膜的孔隙率高达80%,具有3.14 MPa的抗拉强度和61.79%的伸长率。

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