Effect of the molecular weight and its distribution of polyvinylidene fluoride on the relationship between the spinning process, microstructure and properties of hollow fiber membranes via thermally induced phase separation
Source abstract
Abstract
Polyvinylidene fluoride (PVDF) is an important material in the preparation of ultrafiltration membranes via the thermally induced phase separation (TIPS) method. In this paper, four PVDF hollow fiber membranes with different molecular weights were prepared via the TIPS method by using dibutyl phthalate and dioctyl phthalate as a mixed diluent. The relationship between the molecular weight of PVDF and its distribution, phase separation, crystallization behavior and spinning process has been systematically studied. The effects of three factors on the microstructure and properties of the PVDF membrane have been analyzed. The flow behaviors of the PVDF/diluent and PVDF melt were tested by a capillary rheometer and a melt flow rate instrument, respectively. A phase diagram of the membrane solution was determined by thermal polarizing microscope and differential scanning calorimetry. The crystallization behavior and angle of orientation of the membrane were tested by using a differential scanning calorimeter and a sound velocity orientation measurement instrument. The microstructures, such as the pore structure and crystalline grain structure, were observed by field emission scanning electron microscopy. Meanwhile, the properties of the membrane were examined from the view of water flux, porosity and tensile testing. The results showed that changes in the polymer molecular weights affected not only the dynamics but also the thermodynamics of phase separation in membrane formation. As the PVDF molecular weight increased, the phase separation region increased, but the membrane structure became denser. A wide molecular weight distribution easily produced large pores. Then, the water flux decreased first and then increased.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Membrane Separation Technologies · Membrane Separation and Gas Transport · Membrane-based Ion Separation Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Separation Membranes and Membrane Processes/National Center for International Research on Membrane Science and Technology, Tianjin Polytechnic University, China
Textile Institute, Tianjin Polytechnic University, China
Inner Mongolia 3F Wanhao Fluorine Chemical Co., Ltd, China
Funding
National Natural Science Foundation of China · Program Scholars and for Chang-jiang Innovative Research Team in University of Ministry of Education of China · Science and Technology Plans of Tianjin
References (19)
Show source-provided references
1. 10.1016/j.memsci.2016.08.01810.1016/j.memsci.2016.08.018 ↗
2. 10.1016/j.memsci.2011.03.01410.1016/j.memsci.2011.03.014 ↗
3. 10.1177/004051751453586910.1177/0040517514535869 ↗
4. 10.1177/004051751452587910.1177/0040517514525879 ↗
5. 10.1016/j.memsci.2016.02.05010.1016/j.memsci.2016.02.050 ↗
6. 10.1016/j.memsci.2008.03.04310.1016/j.memsci.2008.03.043 ↗
7. 10.1016/j.seppur.2012.02.04310.1016/j.seppur.2012.02.043 ↗
8. 10.1016/j.polymer.2014.01.03510.1016/j.polymer.2014.01.035 ↗
9. 10.1016/j.memsci.2014.07.06010.1016/j.memsci.2014.07.060 ↗
10. 10.1016/j.cej.2015.04.03010.1016/j.cej.2015.04.030 ↗
11. Ji GL. Structure control and properties of PVDF microporous membranes prepared by thermally induced phase separation . PhD Thesis, Zhejiang University, China, 2008.
12. 10.1016/j.desal.2015.01.03910.1016/j.desal.2015.01.039 ↗
13. 10.1103/PhysRev.56.97810.1103/PhysRev.56.978 ↗
14. 10.1016/j.memsci.2015.09.02410.1016/j.memsci.2015.09.024 ↗
15. 10.1016/j.mssp.2015.08.00410.1016/j.mssp.2015.08.004 ↗
16. 10.1016/j.eurpolymj.2006.12.03310.1016/j.eurpolymj.2006.12.033 ↗
17. 10.1016/S0376-7388(02)00056-X10.1016/S0376-7388(02)00056-X ↗
18. 10.1016/j.desal.2005.10.01510.1016/j.desal.2005.10.015 ↗
19. Dai W. Preparation of large denier UHMWPE fibers . Master’s Thesis, Donghua University, China, 2016.