Increasing membrane permeability of UV-modified poly(ether sulfone) ultrafiltration membranes
被引:146
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作者:
Pieracci, J
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机构:Rensselaer Polytech Inst, Howard P Isermann Dept Chem Engn, Troy, NY 12180 USA
Pieracci, J
Crivello, JV
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机构:Rensselaer Polytech Inst, Howard P Isermann Dept Chem Engn, Troy, NY 12180 USA
Crivello, JV
Belfort, G
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机构:
Rensselaer Polytech Inst, Howard P Isermann Dept Chem Engn, Troy, NY 12180 USARensselaer Polytech Inst, Howard P Isermann Dept Chem Engn, Troy, NY 12180 USA
Belfort, G
[1
]
机构:
[1] Rensselaer Polytech Inst, Howard P Isermann Dept Chem Engn, Troy, NY 12180 USA
[2] Rensselaer Polytech Inst, New York State Ctr Polymer Synthesis, Troy, NY 12180 USA
membrane surface modification;
UV-assisted graft polymerization;
protein fouling;
chain transfer agents;
wetting agents ultrafiltration;
porous membranes;
D O I:
10.1016/S0376-7388(01)00624-X
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
The use of the chain transfer agent, 2-mercaptoethanol, and ethanol cleaning was successful in producing hydrophilic membranes with higher permeabilities than the unmodified poly(ether sulfone) (PES) membrane. Permeabilities of dip-modified membranes were three to five times higher than with ethanol cleaning alone. Membrane permeability increased by 50% for dip-modified membranes in the presence of a low 2-mercaptoethanol concentration and by 20-200% when high 2-mercaptoethanol concentrations were used. From the lower degree of grafting (DG) achieved. it was inferred that the graft chain density and chain length decreased with increasing concentration of chain transfer agent. However, the observed rejection was severely reduced indicating that dip-modification caused considerable pore enlargement. This was not previously observed because non-grafted homopolymer may have been formed which effectively blocked the pores. It is speculated that ethanol cleaning removed the homopolymer because it wets and possibly swells the membrane pore structure. This indicated that it was not possible to dip-modify 50 kDa PES UF membranes using 300 nm lamps and a benzene filter without causing significant chance to the pore structure. In addition. the combination of irradiation and N-vinyl-2-pyrrolidinone (NVP) caused a more severe loss of observed rejection than irradiation alone. The molecular weight cut-off (MWCO) of membranes irradiated and/or dip-modified with or without 2-mercaptoethanol was estimated to be between 50 and 100 kDa using a calibration curve for observed rejection versus membrane MWCO. The high hydrophilicity, high permeability, and low fouling character of membranes modified with 2-mercaptoethanol and cleaned with ethanol make them desirable for the filtration of larger proteins (>500 kDa) or for applications with smaller proteins in which high protein transmission is required. (C) 2002 Elsevier Science B.V. All rights reserved.
机构:
Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
University of Science and Technology of ChinaKey Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
Sihan Huang
Yaohan Chen
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机构:
Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
University of Science and Technology of ChinaKey Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
Yaohan Chen
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机构:
Xue Wang
Jing Guo
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机构:
Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
University of Science and Technology of ChinaKey Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
Jing Guo
Yonggang Li
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机构:
Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
University of Science and Technology of ChinaKey Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
Yonggang Li
Lei Dai
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机构:
Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of SciencesKey Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
Lei Dai
Shenghai Li
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机构:
Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
University of Science and Technology of ChinaKey Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
机构:
Univ Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, MalaysiaUniv Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia
Lim, Swee Su
Daud, Wan Ramli Wan
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机构:
Univ Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia
Univ Kebangsaan Malaysia, Fac Engn & Built Environm, Dept Chem & Proc Engn, Bangi 43600, MalaysiaUniv Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia
Daud, Wan Ramli Wan
Jahim, Jamaliah Md
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机构:
Univ Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia
Univ Kebangsaan Malaysia, Fac Engn & Built Environm, Dept Chem & Proc Engn, Bangi 43600, MalaysiaUniv Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia
Jahim, Jamaliah Md
Ghasemi, Mostafa
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机构:
Univ Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia
Univ Kebangsaan Malaysia, Fac Engn & Built Environm, Dept Chem & Proc Engn, Bangi 43600, MalaysiaUniv Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia
Ghasemi, Mostafa
Chong, Poh She
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机构:
Univ Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia
Univ Kebangsaan Malaysia, Fac Engn & Built Environm, Dept Chem & Proc Engn, Bangi 43600, MalaysiaUniv Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia
Chong, Poh She
Ismail, Manal
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机构:
Univ Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia
Univ Kebangsaan Malaysia, Fac Engn & Built Environm, Dept Chem & Proc Engn, Bangi 43600, MalaysiaUniv Kebangsaan Malaysia, Fuel Cell Inst, Bangi 43600, Malaysia