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Preparation and characterization of hydrophobic PVDF membranes by vapor-induced phase separation and application in vacuum membrane distillation

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Abstract

Hydrophobic symmetric flat-sheet membranes of polyvinylidene fluoride (PVDF) for use in vacuum membrane distillation (VMD) were successfully fabricated by the vapor-induced phase separation (VIPS) method using the double-layer casting process. To avoid the delamination that often occurs in double-layered membranes, the same PVDF polymer was employed in both the upper layer and support layer casting solutions. Solutions with low and high PVDF contents were co-cast as the upper layer and support layer of the membrane that was formed. In the VIPS process, the low PVDF content solution favored the formation of a layer with a porous and hydrophobic surface, whereas the solution with a high PVDF concentration favored the formation of a layer with high mechanical strength. The effect of the vapor-induced time on the morphological properties of the membranes was studied. As the vapor-induced time was increased, the cross-section of the membrane changed from an asymmetrical finger-like structure to a symmetrical sponge-like structure, and the surface of the membrane became rough and porous. The membrane subjected to the longer vapor-induced time also exhibited a higher permeating flux during the VMD process. The best PVDF membrane fabricated in this study had a mean radial pore size of 0.49 μm, and the rough upper surface produced a static contact angle of 145° with water. During the VMD process with a 3.5 wt.% sodium chloride (NaCl) aqueous solution, the best membrane that was fabricated produced a permeating flux of 22.4 kg m−2 h−1 and an NaCl rejection rate of 99.9 % at a feed temperature of 73 °C and a downstream pressure of 31.5 kPa. This performance is comparable to or superior to the performances of most of the flat-sheet PVDF membranes reported in the literature and a polytetrafluoroethylene membrane used in this study.

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Abbreviations

A :

Effective area of the membrane (m2)

B :

Geometric factor

B a :

Gas permeance coefficient (mol m−2 S−1 Pa−1)

C f :

Concentration in the feed solution (g L−1)

C p :

Concentration in the permeate (g L−1)

I 0 :

Intercept defined in Eq. 2 (mol m−2 S−1 Pa−1)

J :

Permeate flux (kg m−2 h−1)

k B :

Boltzmann constant (J K−1)

L P :

Effective pore length (m)

LEP w :

Water entry pressure (Pa)

M :

Molecular weight of gas (kg mol−1)

P :

Total pressure (Pa)

P m :

Mean pressure (Pa)

ΔP :

Transmembrane pressure (Pa)

P downstream :

Pressure at downstream (Pa)

\( P_{\text{water}}^{\text{vap} } \) :

Vapor pressure of pure water (Pa)

Q :

Total mass of the permeate (kg)

r :

Membrane pore radius (m)

R :

Gas constant (J mol−1 K−1)

R j :

Rejection rate (%)

S 0 :

Slope defined in Eq. 2 (mol m−2 S−1 Pa−2)

T :

Absolute temperature (K)

t :

Running time (h)

α water :

Activity of water

δ :

Membrane thickness (m)

λ :

Mean free path (m)

γ L :

Liquid surface tension (Pa m)

ε :

Porosity (%)

ε/L P :

Effective porosity (m−1)

τ :

Tortuosity of membrane

μ :

Gas viscosity (kg m−1 s−1)

θ :

Liquid/solid contact angle (°)

ρ :

Density (kg m−1 s−1)

σ :

Collision diameter (m)

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Acknowledgements

The authors would like to thank Professor Liu Zhongzhou of the Research Center for Eco-Environmental Science, the Chinese Academy of Sciences, for his valuable discussions and suggestions. The authors also thank the National Natural Science Foundation of China for financial support (21176008).

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Correspondence to Yuelian Peng.

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Fan, H., Peng, Y., Li, Z. et al. Preparation and characterization of hydrophobic PVDF membranes by vapor-induced phase separation and application in vacuum membrane distillation. J Polym Res 20, 134 (2013). https://doi.org/10.1007/s10965-013-0134-4

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