메뉴 건너뛰기




Volumn 449, Issue , 2014, Pages 50-57

Grafting polyzwitterions onto polyamide by click chemistry and nucleophilic substitution on nitrogen: A novel approach to enhance membrane fouling resistance

Author keywords

Antifouling; Click chemistry; Nucleophilic substitution on nitrogen; Polyamide; Polyzwitterion; Surface modification

Indexed keywords

ANTIFOULING; AZIDE-ALKYNE CYCLOADDITION; CLICK CHEMISTRY; MILD REACTION CONDITIONS; NUCLEOPHILIC SUBSTITUTIONS; POLYZWITTERION; REVERSIBLE ADDITION FRAGMENTATION CHAIN TRANSFER; SEMI-PERMEABLE MEMBRANES;

EID: 84883645616     PISSN: 03767388     EISSN: 18733123     Source Type: Journal    
DOI: 10.1016/j.memsci.2013.08.022     Document Type: Article
Times cited : (119)

References (55)
  • 2
    • 72649098701 scopus 로고    scopus 로고
    • Organic fouling of forward osmosis membranes: fouling reversibility and cleaning without chemical reagents
    • Mi B., Elimelech M. Organic fouling of forward osmosis membranes: fouling reversibility and cleaning without chemical reagents. J. Membr. Sci. 2010, 348:337-345.
    • (2010) J. Membr. Sci. , vol.348 , pp. 337-345
    • Mi, B.1    Elimelech, M.2
  • 3
    • 77949354628 scopus 로고    scopus 로고
    • Gypsum scaling and cleaning in forward osmosis: measurements and mechanisms
    • Mi B., Elimelech M. Gypsum scaling and cleaning in forward osmosis: measurements and mechanisms. Environ. Sci. Technol. 2010, 44:2022-2028.
    • (2010) Environ. Sci. Technol. , vol.44 , pp. 2022-2028
    • Mi, B.1    Elimelech, M.2
  • 4
    • 84859586760 scopus 로고    scopus 로고
    • Combined fouling of forward osmosis membranes: synergistic foulant interaction and direct observation of fouling layer formation
    • Liu Y., Mi B. Combined fouling of forward osmosis membranes: synergistic foulant interaction and direct observation of fouling layer formation. J. Membr. Sci. 2012, 407:136-144.
    • (2012) J. Membr. Sci. , vol.407 , pp. 136-144
    • Liu, Y.1    Mi, B.2
  • 6
    • 84865958167 scopus 로고    scopus 로고
    • Surface modification of polypropylene macroporous membrane by marrying RAFT polymerization with click chemistry
    • Wu X.-M., Wang L.-L., Wang Y., Gu J.-S., Yu H.-Y. Surface modification of polypropylene macroporous membrane by marrying RAFT polymerization with click chemistry. J. Membr. Sci. 2012, 421-422:60-68.
    • (2012) J. Membr. Sci. , pp. 60-68
    • Wu, X.-M.1    Wang, L.-L.2    Wang, Y.3    Gu, J.-S.4    Yu, H.-Y.5
  • 7
    • 34548247597 scopus 로고    scopus 로고
    • Combination of living radical polymerization and click chemistry for surface modification
    • Ranjan R., Brittain W.J. Combination of living radical polymerization and click chemistry for surface modification. Macromolecules 2007, 40:6217-6223.
    • (2007) Macromolecules , vol.40 , pp. 6217-6223
    • Ranjan, R.1    Brittain, W.J.2
  • 8
    • 34547272503 scopus 로고    scopus 로고
    • The growing applications of click chemistry
    • Moses J.E., Moorhouse A.D. The growing applications of click chemistry. Chem. Soc. Rev. 2007, 36:1249-1262.
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1249-1262
    • Moses, J.E.1    Moorhouse, A.D.2
  • 9
    • 67651095676 scopus 로고    scopus 로고
    • Using click chemistry to fabricate ultrathin thermoresponsive microcapsules through direct covalent layer-by-layer assembly
    • Huang C.J., Chang F.C. Using click chemistry to fabricate ultrathin thermoresponsive microcapsules through direct covalent layer-by-layer assembly. Macromolecules 2009, 42:5155-5166.
    • (2009) Macromolecules , vol.42 , pp. 5155-5166
    • Huang, C.J.1    Chang, F.C.2
  • 10
    • 20444487045 scopus 로고    scopus 로고
    • Combining atom transfer radical polymerization and click chemistry: a versatile method for the preparation of end-functional polymers
    • Lutz J.F., Borner H.G., Weichenhan K. Combining atom transfer radical polymerization and click chemistry: a versatile method for the preparation of end-functional polymers. Macromol. Rap. Commun. 2005, 26:514-518.
    • (2005) Macromol. Rap. Commun. , vol.26 , pp. 514-518
    • Lutz, J.F.1    Borner, H.G.2    Weichenhan, K.3
  • 11
    • 55349136249 scopus 로고    scopus 로고
    • Smart surface of gold nanoparticles fabricated by combination of RAFT and click chemistry
    • Zhang T., Zheng Z., Ding X., Peng Y. Smart surface of gold nanoparticles fabricated by combination of RAFT and click chemistry. Macromol. Rap. Commun. 2008, 29:1716-1720.
    • (2008) Macromol. Rap. Commun. , vol.29 , pp. 1716-1720
    • Zhang, T.1    Zheng, Z.2    Ding, X.3    Peng, Y.4
  • 12
    • 72949124611 scopus 로고    scopus 로고
    • Macromolecular brushes synthesized by grafting from approach based on click chemistry and RAFT polymerization
    • Wu D.X., Song X.H., Tang T., Zhao H.Y. Macromolecular brushes synthesized by grafting from approach based on click chemistry and RAFT polymerization. J. Polym. Sci. Part A Polym. Chem. 2010, 48:443-453.
    • (2010) J. Polym. Sci. Part A Polym. Chem. , vol.48 , pp. 443-453
    • Wu, D.X.1    Song, X.H.2    Tang, T.3    Zhao, H.Y.4
  • 13
    • 84864437342 scopus 로고    scopus 로고
    • One-pot RAFT/click chemistry via isocyanates: efficient synthesis of α-end-functionalized polymers
    • Gody G., Rossner C., Moraes J., Vana P., Maschmeyer T., Perrier S. One-pot RAFT/click chemistry via isocyanates: efficient synthesis of α-end-functionalized polymers. J. Am. Chem. Soc. 2012, 134:12596-12603.
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 12596-12603
    • Gody, G.1    Rossner, C.2    Moraes, J.3    Vana, P.4    Maschmeyer, T.5    Perrier, S.6
  • 14
    • 84866415150 scopus 로고    scopus 로고
    • Pore surface engineering with controlled loadings of functional groups via click chemistry in highly stable metal-organic frameworks
    • Jiang H.-L., Feng D., Liu T.-F., Li J.-R., Zhou H.-C. Pore surface engineering with controlled loadings of functional groups via click chemistry in highly stable metal-organic frameworks. J. Am. Chem. Soc. 2012, 134:14690-14693.
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 14690-14693
    • Jiang, H.-L.1    Feng, D.2    Liu, T.-F.3    Li, J.-R.4    Zhou, H.-C.5
  • 15
    • 33748517626 scopus 로고    scopus 로고
    • Azide/alkyne-click reactions: applications in material science and organic synthesis
    • Binder W.H., Kluger C. Azide/alkyne-click reactions: applications in material science and organic synthesis. Curr. Org. Chem. 2006, 10:1791-1815.
    • (2006) Curr. Org. Chem. , vol.10 , pp. 1791-1815
    • Binder, W.H.1    Kluger, C.2
  • 17
    • 34547179800 scopus 로고    scopus 로고
    • Graft copolymers by a combination of ATRP and two different consecutive click reactions
    • Tsarevsky N.V., Bencherif S.A., Matyjaszewski K. Graft copolymers by a combination of ATRP and two different consecutive click reactions. Macromolecules 2007, 40:4439-4445.
    • (2007) Macromolecules , vol.40 , pp. 4439-4445
    • Tsarevsky, N.V.1    Bencherif, S.A.2    Matyjaszewski, K.3
  • 18
    • 84870368766 scopus 로고    scopus 로고
    • Nucleophilic substitution reaction at the nitrogen of arylsulfonamides with phosphide anion
    • Yoshida S., Igawa K., Tomooka K. Nucleophilic substitution reaction at the nitrogen of arylsulfonamides with phosphide anion. J. Am. Chem. Soc. 2012, 134:19358-19361.
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 19358-19361
    • Yoshida, S.1    Igawa, K.2    Tomooka, K.3
  • 19
    • 71649083968 scopus 로고    scopus 로고
    • Synthesis of nitrogen heterocycle-fused 1,2,4-benzothiadiazine-1,1-dioxide, quinazolinone, and pyrrolidinone derivatives with a guanidine joint via sequential aza-Wittig reaction/intramolecular NH-addition cyclization/nucleophilic substitution ring closure methodology, using functionalyzed carbodiimides as key intermediates
    • Hirota S., Sakai T., Kitamura N., Kubokawa K., Kutsumura N., Otani T., Saito T. Synthesis of nitrogen heterocycle-fused 1,2,4-benzothiadiazine-1,1-dioxide, quinazolinone, and pyrrolidinone derivatives with a guanidine joint via sequential aza-Wittig reaction/intramolecular NH-addition cyclization/nucleophilic substitution ring closure methodology, using functionalyzed carbodiimides as key intermediates. Tetrahedron 2010, 66:653-662.
    • (2010) Tetrahedron , vol.66 , pp. 653-662
    • Hirota, S.1    Sakai, T.2    Kitamura, N.3    Kubokawa, K.4    Kutsumura, N.5    Otani, T.6    Saito, T.7
  • 20
    • 0036495579 scopus 로고    scopus 로고
    • Nucleophilic substitution reaction on the nitrogen of indole nucleus: a novel synthesis of 1-aryltryptamines
    • Hayashi T., Peng W., Nakai Y.Y., Yamada K., Somei M. Nucleophilic substitution reaction on the nitrogen of indole nucleus: a novel synthesis of 1-aryltryptamines. Heterocycles 2002, 57:421-424.
    • (2002) Heterocycles , vol.57 , pp. 421-424
    • Hayashi, T.1    Peng, W.2    Nakai, Y.Y.3    Yamada, K.4    Somei, M.5
  • 21
    • 0035281353 scopus 로고    scopus 로고
    • Nucleophilic substitution reaction on the nitrogen of indole nucleus: formation of 1-(indol-3-yl)indoles upon reaction of 1-hydroxyindoles with indole in formic acid
    • Somei M., Yamada F., Hayashi T., Goto A., Saga Y. Nucleophilic substitution reaction on the nitrogen of indole nucleus: formation of 1-(indol-3-yl)indoles upon reaction of 1-hydroxyindoles with indole in formic acid. Heterocycles 2001, 55:457-460.
    • (2001) Heterocycles , vol.55 , pp. 457-460
    • Somei, M.1    Yamada, F.2    Hayashi, T.3    Goto, A.4    Saga, Y.5
  • 22
    • 0035567873 scopus 로고    scopus 로고
    • Gas phase reactions of NH2Cl with anionic nucleophiles: nucleophilic substitution at neutral nitrogen
    • Gareyev R., Kato S., Bierbaum V.M. Gas phase reactions of NH2Cl with anionic nucleophiles: nucleophilic substitution at neutral nitrogen. J. Am. Soc. Mass Spectrom. 2001, 12:139-143.
    • (2001) J. Am. Soc. Mass Spectrom. , vol.12 , pp. 139-143
    • Gareyev, R.1    Kato, S.2    Bierbaum, V.M.3
  • 23
    • 45949124869 scopus 로고
    • Nitrogen bridgehead compounds part 59. Nucleophilic substitution reactions of 9-bromo-6,7,8,9-tetrahydro-4H-pyrido [1,2-a] pyrimidin-4-ones
    • Bitter I., Tóth G., Hermecz I., Mészros Z. Nitrogen bridgehead compounds part 59. Nucleophilic substitution reactions of 9-bromo-6,7,8,9-tetrahydro-4H-pyrido [1,2-a] pyrimidin-4-ones. Heterocycles 1987, 26:869-873.
    • (1987) Heterocycles , vol.26 , pp. 869-873
    • Bitter, I.1    Tóth, G.2    Hermecz, I.3    Mészros, Z.4
  • 24
    • 37049106961 scopus 로고
    • Metal complexes of sulphur-nitrogen chelating agents. Part 11. Synthesis, characterisation, and thermodynamics of nucleophilic substitution reactions of monohalogeno nickel(II) complexes of tridentate ligands of the type SNN in solution and the solid state
    • Roy R., Chaudhury M., Mondal S.K., Nag K. Metal complexes of sulphur-nitrogen chelating agents. Part 11. Synthesis, characterisation, and thermodynamics of nucleophilic substitution reactions of monohalogeno nickel(II) complexes of tridentate ligands of the type SNN in solution and the solid state. J. Chem. Soc.: Dalton Trans. 1984, 1681-1686.
    • (1984) J. Chem. Soc.: Dalton Trans. , pp. 1681-1686
    • Roy, R.1    Chaudhury, M.2    Mondal, S.K.3    Nag, K.4
  • 25
    • 33845550766 scopus 로고
    • SRN1 mechanism in heteroaromatic nucleophilic substitution. Reactions involving certain dihalogenated π-deficient nitrogen heterocycles
    • Carver D.R., Greenwood T.D., Hubbard J.S., Komin A.P., Sachdeva Y.P., Wolfe J.F. SRN1 mechanism in heteroaromatic nucleophilic substitution. Reactions involving certain dihalogenated π-deficient nitrogen heterocycles. J. Org. Chem. 1983, 48:1180-1185.
    • (1983) J. Org. Chem. , vol.48 , pp. 1180-1185
    • Carver, D.R.1    Greenwood, T.D.2    Hubbard, J.S.3    Komin, A.P.4    Sachdeva, Y.P.5    Wolfe, J.F.6
  • 26
    • 0001648818 scopus 로고
    • Mechanisms for reactions of halogenated compounds. Part 4.[1] activating influences of ring-nitrogen and trifluoromethyl in nucleophilic aromatic substitution
    • Chambers R.D., Martin P.A., Waterhouse J.S., Williams D.L.H., Anderson B. Mechanisms for reactions of halogenated compounds. Part 4.[1] activating influences of ring-nitrogen and trifluoromethyl in nucleophilic aromatic substitution. J. Fluorine Chem. 1982, 20:507-514.
    • (1982) J. Fluorine Chem. , vol.20 , pp. 507-514
    • Chambers, R.D.1    Martin, P.A.2    Waterhouse, J.S.3    Williams, D.L.H.4    Anderson, B.5
  • 27
    • 0000678207 scopus 로고
    • Mechanisms of alkoxide substitution reactions at the carbon-nitrogen double bond. Stereoelectronic control during nucleophilic substitution
    • Johnson J.E., Nalley E.A., Weidig C., Arfan M. Mechanisms of alkoxide substitution reactions at the carbon-nitrogen double bond. Stereoelectronic control during nucleophilic substitution. J. Org. Chem. 1981, 46:3623-3629.
    • (1981) J. Org. Chem. , vol.46 , pp. 3623-3629
    • Johnson, J.E.1    Nalley, E.A.2    Weidig, C.3    Arfan, M.4
  • 28
    • 4043094419 scopus 로고
    • Nucleophilic substitution on nitrogen. Kinetics of reactions of hydroxylamine-O-sulfonic acid in dimethyl sulfoxide-water solvents
    • Sudbury B.A., Krueger J.H. Nucleophilic substitution on nitrogen. Kinetics of reactions of hydroxylamine-O-sulfonic acid in dimethyl sulfoxide-water solvents. Inorg. Chem. 1974, 13:1736-1741.
    • (1974) Inorg. Chem. , vol.13 , pp. 1736-1741
    • Sudbury, B.A.1    Krueger, J.H.2
  • 29
    • 4043111589 scopus 로고
    • Nucleophilic substitution on nitrogen. Reactions of hydroxylamine-O-sulfonate with thiosulfate and thiourea
    • Blanchet P.F., Krueger J.H. Nucleophilic substitution on nitrogen. Reactions of hydroxylamine-O-sulfonate with thiosulfate and thiourea. Inorg. Chem. 1974, 13:719-723.
    • (1974) Inorg. Chem. , vol.13 , pp. 719-723
    • Blanchet, P.F.1    Krueger, J.H.2
  • 30
    • 49549169249 scopus 로고
    • Kinetic study of nucleophilic substitution reaction on nitrogen atom
    • Oae S., Yamamoto F. Kinetic study of nucleophilic substitution reaction on nitrogen atom. Tetrahedron Lett. 1973, 14:5143-5146.
    • (1973) Tetrahedron Lett. , vol.14 , pp. 5143-5146
    • Oae, S.1    Yamamoto, F.2
  • 31
    • 4043139646 scopus 로고
    • Nucleophilic substitution on nitrogen. Kinetics of reactions of hydroxylamine-O-sulfonate ion
    • Krueger J.H., Blanchet P.F., Lee A.P., Sudbury B.A. Nucleophilic substitution on nitrogen. Kinetics of reactions of hydroxylamine-O-sulfonate ion. Inorg. Chem. 1973, 12:2714-2718.
    • (1973) Inorg. Chem. , vol.12 , pp. 2714-2718
    • Krueger, J.H.1    Blanchet, P.F.2    Lee, A.P.3    Sudbury, B.A.4
  • 32
    • 37049130672 scopus 로고
    • A nitrogen isotope effect study of an aromatic nucleophilic substitution reaction
    • Ayrey G., Wylie W.A. A nitrogen isotope effect study of an aromatic nucleophilic substitution reaction. J. Chem. Soc. B: Phys. Org. 1970, 738-739.
    • (1970) J. Chem. Soc. B: Phys. Org. , pp. 738-739
    • Ayrey, G.1    Wylie, W.A.2
  • 33
    • 34250610065 scopus 로고
    • Stereochmeistry of heterocyclic compounds - Communication 11. Effect of substitution on the nitrogen on the configuration of octahydro-4(1H)-quinolones, and the stereochemistry of some nucleophilic reactions at the keto group
    • Mistryukov E.A., Aronova N.I., Kucherov V.F. Stereochmeistry of heterocyclic compounds - Communication 11. Effect of substitution on the nitrogen on the configuration of octahydro-4(1H)-quinolones, and the stereochemistry of some nucleophilic reactions at the keto group. Bull. Acad. Sci. USSR Div. Chem. Sci. 1963, 11:1514-1518.
    • (1963) Bull. Acad. Sci. USSR Div. Chem. Sci. , vol.11 , pp. 1514-1518
    • Mistryukov, E.A.1    Aronova, N.I.2    Kucherov, V.F.3
  • 34
    • 84859550812 scopus 로고    scopus 로고
    • Copper-catalyzed amination of arylboronates with N,N-dialkylhydroxylamines
    • Matsuda N., Hirano K., Satoh T., Miura M. Copper-catalyzed amination of arylboronates with N,N-dialkylhydroxylamines. Angew. Chem. Int. Ed. 2012, 51:3642-3645.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 3642-3645
    • Matsuda, N.1    Hirano, K.2    Satoh, T.3    Miura, M.4
  • 35
    • 77950199173 scopus 로고    scopus 로고
    • Transition-metal-free electrophilic amination between aryl grignard reagents and N-chloroamines
    • Hatakeyama T., Yoshimoto Y., Ghorai S.K., Nakamura M. Transition-metal-free electrophilic amination between aryl grignard reagents and N-chloroamines. Org. Lett. 2010, 12:1516-1519.
    • (2010) Org. Lett. , vol.12 , pp. 1516-1519
    • Hatakeyama, T.1    Yoshimoto, Y.2    Ghorai, S.K.3    Nakamura, M.4
  • 36
    • 0035353388 scopus 로고    scopus 로고
    • Zwitterionic SAMs that resist nonspecific adsorption of protein from aqueous buffer
    • Holmlin R.E., Chen X., Chapman R.G., Takayama S., Whitesides G.M. Zwitterionic SAMs that resist nonspecific adsorption of protein from aqueous buffer. Langmuir 2001, 17:2841-2850.
    • (2001) Langmuir , vol.17 , pp. 2841-2850
    • Holmlin, R.E.1    Chen, X.2    Chapman, R.G.3    Takayama, S.4    Whitesides, G.M.5
  • 37
    • 53249154630 scopus 로고    scopus 로고
    • Preparation and characterizations of novel zwitterionic membranes
    • Liu J.S., Zhan Y., Xu T.W., Shao G.Q. Preparation and characterizations of novel zwitterionic membranes. J. Membr. Sci. 2008, 325:495-502.
    • (2008) J. Membr. Sci. , vol.325 , pp. 495-502
    • Liu, J.S.1    Zhan, Y.2    Xu, T.W.3    Shao, G.Q.4
  • 38
    • 67649341972 scopus 로고    scopus 로고
    • PEG-coated reverse osmosis membranes: desalination properties and fouling resistance
    • Sagle A., Van Wagner E., Ju H., McCloskey B., Freeman B., Sharma M. PEG-coated reverse osmosis membranes: desalination properties and fouling resistance. J. Membr. Sci. 2009, 340:92-108.
    • (2009) J. Membr. Sci. , vol.340 , pp. 92-108
    • Sagle, A.1    Van Wagner, E.2    Ju, H.3    McCloskey, B.4    Freeman, B.5    Sharma, M.6
  • 41
    • 44249103455 scopus 로고    scopus 로고
    • Zwitterionic polyethersulfone ultrafiltration membrane with superior antifouling property
    • Shi Q., Su Y.L., Zhao W., Li C., Hu Y.H., Jiang Z.Y., Zhu S.P. Zwitterionic polyethersulfone ultrafiltration membrane with superior antifouling property. J. Membr. Sci. 2008, 319:271-278.
    • (2008) J. Membr. Sci. , vol.319 , pp. 271-278
    • Shi, Q.1    Su, Y.L.2    Zhao, W.3    Li, C.4    Hu, Y.H.5    Jiang, Z.Y.6    Zhu, S.P.7
  • 43
    • 67649359301 scopus 로고    scopus 로고
    • Highly efficient antifouling ultrafiltration membranes incorporating zwitterionic poly(3-(methacryloylamino)propyl-dimethyl(3-sulfopropyl) ammonium hydroxide)
    • Wang L.J., Su Y.L., Zheng L.L., Chen W.J., Jiang Z.Y. Highly efficient antifouling ultrafiltration membranes incorporating zwitterionic poly(3-(methacryloylamino)propyl-dimethyl(3-sulfopropyl) ammonium hydroxide). J. Membr. Sci. 2009, 340:164-170.
    • (2009) J. Membr. Sci. , vol.340 , pp. 164-170
    • Wang, L.J.1    Su, Y.L.2    Zheng, L.L.3    Chen, W.J.4    Jiang, Z.Y.5
  • 44
    • 77955664970 scopus 로고    scopus 로고
    • Surface hydrophilization of microporous polypropylene membrane by grafting zwitterionic polymer for anti-biofouling
    • Yang Y.F., Li Y., Li Q.L., Wan L.S., Xu Z.K. Surface hydrophilization of microporous polypropylene membrane by grafting zwitterionic polymer for anti-biofouling. J. Membr. Sci. 2010, 362:255-264.
    • (2010) J. Membr. Sci. , vol.362 , pp. 255-264
    • Yang, Y.F.1    Li, Y.2    Li, Q.L.3    Wan, L.S.4    Xu, Z.K.5
  • 45
    • 68049132853 scopus 로고    scopus 로고
    • Enhancing antifouling property of polysulfone ultrafiltration membrane by grafting zwitterionic copolymer via UV-initiated polymerization
    • Yu H.J., Cao Y.M., Kang G.D., Liu J.H., Li M., Yuan Q. Enhancing antifouling property of polysulfone ultrafiltration membrane by grafting zwitterionic copolymer via UV-initiated polymerization. J. Membr. Sci. 2009, 342:6-13.
    • (2009) J. Membr. Sci. , vol.342 , pp. 6-13
    • Yu, H.J.1    Cao, Y.M.2    Kang, G.D.3    Liu, J.H.4    Li, M.5    Yuan, Q.6
  • 46
    • 79251632014 scopus 로고    scopus 로고
    • Improved biocompatibility and antifouling property of polypropylene non-woven fabric membrane by surface grafting zwitterionic polymer
    • Zhao J., Shi Q.A., Luan S.F., Song L.J., Yang H.W., Shi H.C., Jin J., Li X.L., Yin J.H., Stagnaro P. Improved biocompatibility and antifouling property of polypropylene non-woven fabric membrane by surface grafting zwitterionic polymer. J. Membr. Sci. 2011, 369:5-12.
    • (2011) J. Membr. Sci. , vol.369 , pp. 5-12
    • Zhao, J.1    Shi, Q.A.2    Luan, S.F.3    Song, L.J.4    Yang, H.W.5    Shi, H.C.6    Jin, J.7    Li, X.L.8    Yin, J.H.9    Stagnaro, P.10
  • 47
    • 79952168710 scopus 로고    scopus 로고
    • Surface-tethered zwitterionic ultrathin antifouling coatings on reverse osmosis membranes by initiated chemical vapor deposition
    • Yang R., Xu J.J., Ozaydin-Ince G., Wong S.Y., Gleason K.K. Surface-tethered zwitterionic ultrathin antifouling coatings on reverse osmosis membranes by initiated chemical vapor deposition. Chem. Mater. 2011, 23:1263-1272.
    • (2011) Chem. Mater. , vol.23 , pp. 1263-1272
    • Yang, R.1    Xu, J.J.2    Ozaydin-Ince, G.3    Wong, S.Y.4    Gleason, K.K.5
  • 48
    • 79960501888 scopus 로고    scopus 로고
    • Bacterial attachment to RO membranes surface-modified by concentration-polarization-enhanced graft polymerization
    • Bernstein R., Belfer S., Freger V. Bacterial attachment to RO membranes surface-modified by concentration-polarization-enhanced graft polymerization. Environ. Sci. Technol. 2011, 45:5973-5980.
    • (2011) Environ. Sci. Technol. , vol.45 , pp. 5973-5980
    • Bernstein, R.1    Belfer, S.2    Freger, V.3
  • 49
    • 0942300353 scopus 로고    scopus 로고
    • Hydrolysis of microporous polyamide-6 membranes as substrate for in situ synthesis of oligonucleotides
    • Tang J., He N., Nie L., Xiao P., Chen H. Hydrolysis of microporous polyamide-6 membranes as substrate for in situ synthesis of oligonucleotides. Surf. Sci. 2004, 550:26-34.
    • (2004) Surf. Sci. , vol.550 , pp. 26-34
    • Tang, J.1    He, N.2    Nie, L.3    Xiao, P.4    Chen, H.5
  • 50
    • 84989606879 scopus 로고
    • The structure of the collodionmembrane and its electrical behavior 12: the preparation and properties of "megapermselective" protamine collodion membranes combining high ionic selectivity with high permeability
    • C.W. Carr, H.P. Gregor, K. Sollner, The structure of the collodionmembrane and its electrical behavior 12: the preparation and properties of "megapermselective" protamine collodion membranes combining high ionic selectivity with high permeability. J. Gen. Physiol. 28 (1945) 179-185.
    • (1945) J. Gen. Physiol. , vol.28 , pp. 179-185
    • Carr, C.W.1    Gregor, H.P.2    Sollner, K.3
  • 51
    • 34547924488 scopus 로고    scopus 로고
    • Study on hypochlorite degradation of aromatic polyamide reverse osmosis membrane
    • Kang G.-D., Gao C.-J., Chen W.-D., Jie X.-M., Cao Y.-M., Yuan Q. Study on hypochlorite degradation of aromatic polyamide reverse osmosis membrane. J. Membr. Sci. 2007, 300:165-171.
    • (2007) J. Membr. Sci. , vol.300 , pp. 165-171
    • Kang, G.-D.1    Gao, C.-J.2    Chen, W.-D.3    Jie, X.-M.4    Cao, Y.-M.5    Yuan, Q.6
  • 52
    • 84862909272 scopus 로고    scopus 로고
    • Surface-grafted zwitterionic polymers as platforms for functional supported phospholipid membranes
    • Santonicola M.G., Memesa M., Meszyńska A., Ma Y., Vancso G.J. Surface-grafted zwitterionic polymers as platforms for functional supported phospholipid membranes. Soft Matter 2012, 8:1556-1562.
    • (2012) Soft Matter , vol.8 , pp. 1556-1562
    • Santonicola, M.G.1    Memesa, M.2    Meszyńska, A.3    Ma, Y.4    Vancso, G.J.5
  • 53
    • 34547768816 scopus 로고    scopus 로고
    • Functionalization of nylon membranes via surface-initiated atom-transfer radical polymerization
    • Xu F.J., Zhao J.P., Kang E.T., Neoh K.G., Li J. Functionalization of nylon membranes via surface-initiated atom-transfer radical polymerization. Langmuir 2007, 23:8585-8592.
    • (2007) Langmuir , vol.23 , pp. 8585-8592
    • Xu, F.J.1    Zhao, J.P.2    Kang, E.T.3    Neoh, K.G.4    Li, J.5
  • 54
    • 68249114790 scopus 로고    scopus 로고
    • Temperature- and pH-sensitive nylon membranes prepared via consecutive surface-initiated atom transfer radical graft polymerizations
    • Zhang Z.B., Zhu X.L., Xu F.J., Neoh K.G., Kang E.T. Temperature- and pH-sensitive nylon membranes prepared via consecutive surface-initiated atom transfer radical graft polymerizations. J. Membr. Sci. 2009, 342:300-306.
    • (2009) J. Membr. Sci. , vol.342 , pp. 300-306
    • Zhang, Z.B.1    Zhu, X.L.2    Xu, F.J.3    Neoh, K.G.4    Kang, E.T.5
  • 55
    • 48549094689 scopus 로고    scopus 로고
    • Chemical and physical aspects of organic fouling of forward osmosis membranes
    • Mi B., Elimelech M. Chemical and physical aspects of organic fouling of forward osmosis membranes. J. Membr. Sci. 2008, 320:292-302.
    • (2008) J. Membr. Sci. , vol.320 , pp. 292-302
    • Mi, B.1    Elimelech, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.