The polyvinylidene fluoride (PVDF)-diphenyl ketone (DPK) mixture was studied as a new system to prepare PVDF membranes via thermally induced phase separation (TIPS). The phenomena of liquid-liquid phase separation was found in this mixture when the temperature of mixture was decreasing and the PVDF concentration was less than 30 wt %. Using DPK as diluent, PVDF membrane with bicontinuous structure was obtained without necessity to add a nonsolvent or a stretching process further. The phase diagram of PVDF-DPK system was also constructed to help investigate the effect of PVDF concentration and coarsening temperature on morphology of resulting membrane.The experiments showed that high coarsening temperatures and low PVDF concentrations resulted in the formation of the large pore size membrane. The strength of the wet membrane was decreasing with decreasing PVDF concentration. On condition that the PVDF concentration was larger than 30 wt %, thermally induced solid-liquid separation occurred and bicontinuous structure disappeared.
Diphenyl carbonate was used as a diluent to prepare microporous polyvinylidene fluoride (PVDF) membrane via thermally induced phase-separation method. The liquid-liquid phase-separation phenomenon was found in PVDF/diphenyl carbonate system during the thermally induced phase-separation process. The monotectic point of this system appeared at a high polymer concentration approximately 56 wt %. This suggested that PVDF membrane with a bicontinuous or cellular structure could be obtained when the PVDF concentration was less than this point value. The effects of polymer concentration and quenching temperature on the membrane structure, porosity, and tensile strength were also investigated. The results showed that low polymer concentration and high quenching temperature led to a large pore size membrane. The tensile strength of the membrane increased with increase in the polymer concentration, but the porosity of the membrane decreased. On condition that the PVDF concentration was higher than 60 wt %, only polymer crystallization occurred and a typical compact spherulitic structure was obtained.
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