4.7 Article

Controlling the inner surface pore and spherulite structures of PVDF hollow fiber membranes in thermally induced phase separation using triple-orifice for membrane distillation

Journal

SEPARATION AND PURIFICATION TECHNOLOGY
Volume 258, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.seppur.2020.117988

Keywords

PVDF hollow fiber membranes; Inner surface structure; Triple-orifice spinneret; Membrane distillation; Thermally induced phase separation

Funding

  1. China Scholarship Council (CSC), China [201808050053]

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This study focused on controlling the inner surface structures of PVDF hollow fiber membranes for DCMD by using different bore liquids with varying compatibilities with the diluent and polymer. The compatibility of the bore liquids was found to significantly impact the inner surface pore size and spherulite structures, ultimately affecting the membrane's water vapor permeability, hydrophobicity, liquid entry pressure, salt rejection, and wetting resistance. This research provides valuable insights for selecting appropriate bore liquids to prepare high-performance hollow fiber membranes with desired inner surface structures.
In this study, we controlled the inner surface structures of polyvinylidene fluoride (PVDF) hollow fiber membranes via a thermally induced phase separation process using a triple-orifice spinneret for direct-contact membrane distillation (DCMD). The coextrusion of propylene carbonate (PC) through the outermost channel of the spinneret led to porous outer surfaces with similar pore sizes and spherulitic structures for all the PVDF hollow fiber membranes. In the innermost channel, the extrusion of solvents having different compatibilities with PVDF and the diluent (PC) as the bore liquids controlled the inner surface pore sizes and spherulite structures, and the effects of these inner surface structures on the DCMD performance were investigated in detail. Increasing the compatibility of the bore liquids toward the diluent led to an increase in the inner surface pore size because of the formation of loose, isolated spherulites, which remarkably enhanced the water vapor permeability from 4 to 8.3 L m(2) h(-1), while reducing the membrane hydrophobicity, liquid entry pressure, and salt rejection. When increasing the bore liquid compatibility with the polymer, the surface pore size decreased because of the tight spherulite contact, enhancing membrane salt rejection and wetting resistance. Given the significance of bore liquid compatibility with the diluent and the polymer in controlling the inner surface structures, a useful guideline is presented for selecting the appropriate bore liquids to prepare hollow fiber membranes with the desired inner surface structures for high MD performance.

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