High-Flux Direct-Contact Pervaporation Membranes for Desalination
To solve the pore-wetting problems of membrane distillation, we developed a series of three-layer composite pervaporation (PV) membranes that could be applied in direct contact mode. Specifically, a porous poly(vinylidene fluoride) (PVDF) layer was placed on top of a polytetrafluoroethylene (PTFE)...
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Veröffentlicht in: | ACS applied materials & interfaces 2019-08, Vol.11 (31), p.28461-28468 |
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description | To solve the pore-wetting problems of membrane distillation, we developed a series of three-layer composite pervaporation (PV) membranes that could be applied in direct contact mode. Specifically, a porous poly(vinylidene fluoride) (PVDF) layer was placed on top of a polytetrafluoroethylene (PTFE) microfiltration membrane using the nonsolvent-induced phase inversion method, and then a poly(vinyl alcohol) (PVA) dense layer was coated on the PVDF/PTFE substrate. The hydrophobic PTFE layer prevented the permeate side of the PVA/PVDF/PTFE membrane from being wetted with cooling water. The PVDF intermediate layer acted as a glue to the PVA and PTFE layers. Also, the PVA dense layer provided a high water flux, salt rejection, and antifouling property. As a result, a high water flux of 44.5 ± 3.0 kg/(m2 h) with the NaCl rejection of >99.99% were achieved for the direct-contact pervaporation (DCPV) membranes when separating a 3.5 wt % NaCl solution at 75.0 ± 0.9 °C using a cooling water stream of 20.6 ± 0.3 °C. Moreover, when the NaCl solution contained 10 mg/L Tween20 (acting as a contaminant), a stable water flux of 45.8 ± 0.6 kg/(m2 h) was maintained for at least 24 h, indicating excellent antifouling property. Furthermore, when the permeate side was under vacuum, the water flux increased to 83.4 ± 6.5 kg/(m2 h), similar to the highest reported data of all the existing PV desalination membranes. More importantly, the easy-to-scale-up fabrication method indicated great potential of DCPV membranes for commercialization. |
doi_str_mv | 10.1021/acsami.9b08078 |
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Specifically, a porous poly(vinylidene fluoride) (PVDF) layer was placed on top of a polytetrafluoroethylene (PTFE) microfiltration membrane using the nonsolvent-induced phase inversion method, and then a poly(vinyl alcohol) (PVA) dense layer was coated on the PVDF/PTFE substrate. The hydrophobic PTFE layer prevented the permeate side of the PVA/PVDF/PTFE membrane from being wetted with cooling water. The PVDF intermediate layer acted as a glue to the PVA and PTFE layers. Also, the PVA dense layer provided a high water flux, salt rejection, and antifouling property. As a result, a high water flux of 44.5 ± 3.0 kg/(m2 h) with the NaCl rejection of >99.99% were achieved for the direct-contact pervaporation (DCPV) membranes when separating a 3.5 wt % NaCl solution at 75.0 ± 0.9 °C using a cooling water stream of 20.6 ± 0.3 °C. Moreover, when the NaCl solution contained 10 mg/L Tween20 (acting as a contaminant), a stable water flux of 45.8 ± 0.6 kg/(m2 h) was maintained for at least 24 h, indicating excellent antifouling property. Furthermore, when the permeate side was under vacuum, the water flux increased to 83.4 ± 6.5 kg/(m2 h), similar to the highest reported data of all the existing PV desalination membranes. More importantly, the easy-to-scale-up fabrication method indicated great potential of DCPV membranes for commercialization.</description><identifier>ISSN: 1944-8244</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.9b08078</identifier><identifier>PMID: 31294541</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>ACS applied materials & interfaces, 2019-08, Vol.11 (31), p.28461-28468</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a330t-f1cb22b60ffe4ea9b127e8a724d7c8c6c3fe4dcf4112aaef9646139ce8d2b6543</citedby><cites>FETCH-LOGICAL-a330t-f1cb22b60ffe4ea9b127e8a724d7c8c6c3fe4dcf4112aaef9646139ce8d2b6543</cites><orcidid>0000-0002-1548-4218</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acsami.9b08078$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsami.9b08078$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>315,781,785,2766,27080,27928,27929,56742,56792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31294541$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meng, Junquan</creatorcontrib><creatorcontrib>Li, Pei</creatorcontrib><creatorcontrib>Cao, Bing</creatorcontrib><title>High-Flux Direct-Contact Pervaporation Membranes for Desalination</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>To solve the pore-wetting problems of membrane distillation, we developed a series of three-layer composite pervaporation (PV) membranes that could be applied in direct contact mode. Specifically, a porous poly(vinylidene fluoride) (PVDF) layer was placed on top of a polytetrafluoroethylene (PTFE) microfiltration membrane using the nonsolvent-induced phase inversion method, and then a poly(vinyl alcohol) (PVA) dense layer was coated on the PVDF/PTFE substrate. The hydrophobic PTFE layer prevented the permeate side of the PVA/PVDF/PTFE membrane from being wetted with cooling water. The PVDF intermediate layer acted as a glue to the PVA and PTFE layers. Also, the PVA dense layer provided a high water flux, salt rejection, and antifouling property. As a result, a high water flux of 44.5 ± 3.0 kg/(m2 h) with the NaCl rejection of >99.99% were achieved for the direct-contact pervaporation (DCPV) membranes when separating a 3.5 wt % NaCl solution at 75.0 ± 0.9 °C using a cooling water stream of 20.6 ± 0.3 °C. Moreover, when the NaCl solution contained 10 mg/L Tween20 (acting as a contaminant), a stable water flux of 45.8 ± 0.6 kg/(m2 h) was maintained for at least 24 h, indicating excellent antifouling property. Furthermore, when the permeate side was under vacuum, the water flux increased to 83.4 ± 6.5 kg/(m2 h), similar to the highest reported data of all the existing PV desalination membranes. 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Mater. Interfaces</addtitle><date>2019-08-07</date><risdate>2019</risdate><volume>11</volume><issue>31</issue><spage>28461</spage><epage>28468</epage><pages>28461-28468</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><abstract>To solve the pore-wetting problems of membrane distillation, we developed a series of three-layer composite pervaporation (PV) membranes that could be applied in direct contact mode. Specifically, a porous poly(vinylidene fluoride) (PVDF) layer was placed on top of a polytetrafluoroethylene (PTFE) microfiltration membrane using the nonsolvent-induced phase inversion method, and then a poly(vinyl alcohol) (PVA) dense layer was coated on the PVDF/PTFE substrate. The hydrophobic PTFE layer prevented the permeate side of the PVA/PVDF/PTFE membrane from being wetted with cooling water. The PVDF intermediate layer acted as a glue to the PVA and PTFE layers. Also, the PVA dense layer provided a high water flux, salt rejection, and antifouling property. As a result, a high water flux of 44.5 ± 3.0 kg/(m2 h) with the NaCl rejection of >99.99% were achieved for the direct-contact pervaporation (DCPV) membranes when separating a 3.5 wt % NaCl solution at 75.0 ± 0.9 °C using a cooling water stream of 20.6 ± 0.3 °C. Moreover, when the NaCl solution contained 10 mg/L Tween20 (acting as a contaminant), a stable water flux of 45.8 ± 0.6 kg/(m2 h) was maintained for at least 24 h, indicating excellent antifouling property. Furthermore, when the permeate side was under vacuum, the water flux increased to 83.4 ± 6.5 kg/(m2 h), similar to the highest reported data of all the existing PV desalination membranes. More importantly, the easy-to-scale-up fabrication method indicated great potential of DCPV membranes for commercialization.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>31294541</pmid><doi>10.1021/acsami.9b08078</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-1548-4218</orcidid></addata></record> |
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title | High-Flux Direct-Contact Pervaporation Membranes for Desalination |
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