Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties
Abstract Heterogeneous ion-exchange membranes were prepared by mixing small particles of sulfonated poly(1,4-phenylene sulfide) or sulfonated styrene–divinylbenzene copolymer with a matrix polymer. Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible f...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Bouzek, Karel [verfasserIn] Moravcová, Sabina [verfasserIn] Schauer, Jan [verfasserIn] Brožová, Libuše [verfasserIn] Pientka, Zbyněk [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2009 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Journal of applied electrochemistry - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971, 40(2009), 5 vom: 04. Sept., Seite 1005-1018 |
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| Übergeordnetes Werk: |
volume:40 ; year:2009 ; number:5 ; day:04 ; month:09 ; pages:1005-1018 |
| Links: |
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| DOI / URN: |
10.1007/s10800-009-9974-3 |
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| Katalog-ID: |
SPR01330674X |
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| 520 | |a Abstract Heterogeneous ion-exchange membranes were prepared by mixing small particles of sulfonated poly(1,4-phenylene sulfide) or sulfonated styrene–divinylbenzene copolymer with a matrix polymer. Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible fluoroelastomer, rigid polystyrene (all highly hydrophobic) and hydrophilic cellulose prepared by hydrolysis of cellulose acetate butyrate. Membrane morphologies were studied by scanning electron microscopy, IR spectroscopy and density measurements. Subsequently, the membranes were characterised with respect to their swelling in water, electrochemical characteristics and transport properties. Ion-exchange capacity and proton conductivity together with the permeability to hydrogen and methanol were investigated. The important impact of the ion-exchange particles as well as of the polymer matrix used was observed. The increasing rigidity of the polymer matrix resulted in a decrease in membrane permeability, but at the same time in deterioration of its ion-exchange capacity and subsequently of the proton conductivity, too. This was explained in terms of the limited elasticity of the polymer matrix, in each sample under study, which does not allow the ion-exchange particles to swell to an identical degree. | ||
| 650 | 4 | |a Ion-exchange membrane |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Heterogeneous membrane |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Ion-exchange capacity |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Proton conductivity |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Permeability |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Moravcová, Sabina |e verfasserin |4 aut | |
| 700 | 1 | |a Schauer, Jan |e verfasserin |4 aut | |
| 700 | 1 | |a Brožová, Libuše |e verfasserin |4 aut | |
| 700 | 1 | |a Pientka, Zbyněk |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Journal of applied electrochemistry |d Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 |g 40(2009), 5 vom: 04. Sept., Seite 1005-1018 |w (DE-627)302466037 |w (DE-600)1491094-9 |x 1572-8838 |7 nnns |
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10.1007/s10800-009-9974-3 doi (DE-627)SPR01330674X (SPR)s10800-009-9974-3-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl Bouzek, Karel verfasserin aut Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Heterogeneous ion-exchange membranes were prepared by mixing small particles of sulfonated poly(1,4-phenylene sulfide) or sulfonated styrene–divinylbenzene copolymer with a matrix polymer. Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible fluoroelastomer, rigid polystyrene (all highly hydrophobic) and hydrophilic cellulose prepared by hydrolysis of cellulose acetate butyrate. Membrane morphologies were studied by scanning electron microscopy, IR spectroscopy and density measurements. Subsequently, the membranes were characterised with respect to their swelling in water, electrochemical characteristics and transport properties. Ion-exchange capacity and proton conductivity together with the permeability to hydrogen and methanol were investigated. The important impact of the ion-exchange particles as well as of the polymer matrix used was observed. The increasing rigidity of the polymer matrix resulted in a decrease in membrane permeability, but at the same time in deterioration of its ion-exchange capacity and subsequently of the proton conductivity, too. This was explained in terms of the limited elasticity of the polymer matrix, in each sample under study, which does not allow the ion-exchange particles to swell to an identical degree. Ion-exchange membrane (dpeaa)DE-He213 Heterogeneous membrane (dpeaa)DE-He213 Ion-exchange capacity (dpeaa)DE-He213 Proton conductivity (dpeaa)DE-He213 Permeability (dpeaa)DE-He213 Moravcová, Sabina verfasserin aut Schauer, Jan verfasserin aut Brožová, Libuše verfasserin aut Pientka, Zbyněk verfasserin aut Enthalten in Journal of applied electrochemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 40(2009), 5 vom: 04. Sept., Seite 1005-1018 (DE-627)302466037 (DE-600)1491094-9 1572-8838 nnns volume:40 year:2009 number:5 day:04 month:09 pages:1005-1018 https://dx.doi.org/10.1007/s10800-009-9974-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE AR 40 2009 5 04 09 1005-1018 |
| spelling |
10.1007/s10800-009-9974-3 doi (DE-627)SPR01330674X (SPR)s10800-009-9974-3-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl Bouzek, Karel verfasserin aut Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Heterogeneous ion-exchange membranes were prepared by mixing small particles of sulfonated poly(1,4-phenylene sulfide) or sulfonated styrene–divinylbenzene copolymer with a matrix polymer. Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible fluoroelastomer, rigid polystyrene (all highly hydrophobic) and hydrophilic cellulose prepared by hydrolysis of cellulose acetate butyrate. Membrane morphologies were studied by scanning electron microscopy, IR spectroscopy and density measurements. Subsequently, the membranes were characterised with respect to their swelling in water, electrochemical characteristics and transport properties. Ion-exchange capacity and proton conductivity together with the permeability to hydrogen and methanol were investigated. The important impact of the ion-exchange particles as well as of the polymer matrix used was observed. The increasing rigidity of the polymer matrix resulted in a decrease in membrane permeability, but at the same time in deterioration of its ion-exchange capacity and subsequently of the proton conductivity, too. This was explained in terms of the limited elasticity of the polymer matrix, in each sample under study, which does not allow the ion-exchange particles to swell to an identical degree. Ion-exchange membrane (dpeaa)DE-He213 Heterogeneous membrane (dpeaa)DE-He213 Ion-exchange capacity (dpeaa)DE-He213 Proton conductivity (dpeaa)DE-He213 Permeability (dpeaa)DE-He213 Moravcová, Sabina verfasserin aut Schauer, Jan verfasserin aut Brožová, Libuše verfasserin aut Pientka, Zbyněk verfasserin aut Enthalten in Journal of applied electrochemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 40(2009), 5 vom: 04. Sept., Seite 1005-1018 (DE-627)302466037 (DE-600)1491094-9 1572-8838 nnns volume:40 year:2009 number:5 day:04 month:09 pages:1005-1018 https://dx.doi.org/10.1007/s10800-009-9974-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE AR 40 2009 5 04 09 1005-1018 |
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10.1007/s10800-009-9974-3 doi (DE-627)SPR01330674X (SPR)s10800-009-9974-3-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl Bouzek, Karel verfasserin aut Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Heterogeneous ion-exchange membranes were prepared by mixing small particles of sulfonated poly(1,4-phenylene sulfide) or sulfonated styrene–divinylbenzene copolymer with a matrix polymer. Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible fluoroelastomer, rigid polystyrene (all highly hydrophobic) and hydrophilic cellulose prepared by hydrolysis of cellulose acetate butyrate. Membrane morphologies were studied by scanning electron microscopy, IR spectroscopy and density measurements. Subsequently, the membranes were characterised with respect to their swelling in water, electrochemical characteristics and transport properties. Ion-exchange capacity and proton conductivity together with the permeability to hydrogen and methanol were investigated. The important impact of the ion-exchange particles as well as of the polymer matrix used was observed. The increasing rigidity of the polymer matrix resulted in a decrease in membrane permeability, but at the same time in deterioration of its ion-exchange capacity and subsequently of the proton conductivity, too. This was explained in terms of the limited elasticity of the polymer matrix, in each sample under study, which does not allow the ion-exchange particles to swell to an identical degree. Ion-exchange membrane (dpeaa)DE-He213 Heterogeneous membrane (dpeaa)DE-He213 Ion-exchange capacity (dpeaa)DE-He213 Proton conductivity (dpeaa)DE-He213 Permeability (dpeaa)DE-He213 Moravcová, Sabina verfasserin aut Schauer, Jan verfasserin aut Brožová, Libuše verfasserin aut Pientka, Zbyněk verfasserin aut Enthalten in Journal of applied electrochemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 40(2009), 5 vom: 04. Sept., Seite 1005-1018 (DE-627)302466037 (DE-600)1491094-9 1572-8838 nnns volume:40 year:2009 number:5 day:04 month:09 pages:1005-1018 https://dx.doi.org/10.1007/s10800-009-9974-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE AR 40 2009 5 04 09 1005-1018 |
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10.1007/s10800-009-9974-3 doi (DE-627)SPR01330674X (SPR)s10800-009-9974-3-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl Bouzek, Karel verfasserin aut Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Heterogeneous ion-exchange membranes were prepared by mixing small particles of sulfonated poly(1,4-phenylene sulfide) or sulfonated styrene–divinylbenzene copolymer with a matrix polymer. Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible fluoroelastomer, rigid polystyrene (all highly hydrophobic) and hydrophilic cellulose prepared by hydrolysis of cellulose acetate butyrate. Membrane morphologies were studied by scanning electron microscopy, IR spectroscopy and density measurements. Subsequently, the membranes were characterised with respect to their swelling in water, electrochemical characteristics and transport properties. Ion-exchange capacity and proton conductivity together with the permeability to hydrogen and methanol were investigated. The important impact of the ion-exchange particles as well as of the polymer matrix used was observed. The increasing rigidity of the polymer matrix resulted in a decrease in membrane permeability, but at the same time in deterioration of its ion-exchange capacity and subsequently of the proton conductivity, too. This was explained in terms of the limited elasticity of the polymer matrix, in each sample under study, which does not allow the ion-exchange particles to swell to an identical degree. Ion-exchange membrane (dpeaa)DE-He213 Heterogeneous membrane (dpeaa)DE-He213 Ion-exchange capacity (dpeaa)DE-He213 Proton conductivity (dpeaa)DE-He213 Permeability (dpeaa)DE-He213 Moravcová, Sabina verfasserin aut Schauer, Jan verfasserin aut Brožová, Libuše verfasserin aut Pientka, Zbyněk verfasserin aut Enthalten in Journal of applied electrochemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 40(2009), 5 vom: 04. Sept., Seite 1005-1018 (DE-627)302466037 (DE-600)1491094-9 1572-8838 nnns volume:40 year:2009 number:5 day:04 month:09 pages:1005-1018 https://dx.doi.org/10.1007/s10800-009-9974-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE AR 40 2009 5 04 09 1005-1018 |
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10.1007/s10800-009-9974-3 doi (DE-627)SPR01330674X (SPR)s10800-009-9974-3-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl Bouzek, Karel verfasserin aut Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Heterogeneous ion-exchange membranes were prepared by mixing small particles of sulfonated poly(1,4-phenylene sulfide) or sulfonated styrene–divinylbenzene copolymer with a matrix polymer. Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible fluoroelastomer, rigid polystyrene (all highly hydrophobic) and hydrophilic cellulose prepared by hydrolysis of cellulose acetate butyrate. Membrane morphologies were studied by scanning electron microscopy, IR spectroscopy and density measurements. Subsequently, the membranes were characterised with respect to their swelling in water, electrochemical characteristics and transport properties. Ion-exchange capacity and proton conductivity together with the permeability to hydrogen and methanol were investigated. The important impact of the ion-exchange particles as well as of the polymer matrix used was observed. The increasing rigidity of the polymer matrix resulted in a decrease in membrane permeability, but at the same time in deterioration of its ion-exchange capacity and subsequently of the proton conductivity, too. This was explained in terms of the limited elasticity of the polymer matrix, in each sample under study, which does not allow the ion-exchange particles to swell to an identical degree. Ion-exchange membrane (dpeaa)DE-He213 Heterogeneous membrane (dpeaa)DE-He213 Ion-exchange capacity (dpeaa)DE-He213 Proton conductivity (dpeaa)DE-He213 Permeability (dpeaa)DE-He213 Moravcová, Sabina verfasserin aut Schauer, Jan verfasserin aut Brožová, Libuše verfasserin aut Pientka, Zbyněk verfasserin aut Enthalten in Journal of applied electrochemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 40(2009), 5 vom: 04. Sept., Seite 1005-1018 (DE-627)302466037 (DE-600)1491094-9 1572-8838 nnns volume:40 year:2009 number:5 day:04 month:09 pages:1005-1018 https://dx.doi.org/10.1007/s10800-009-9974-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE AR 40 2009 5 04 09 1005-1018 |
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Enthalten in Journal of applied electrochemistry 40(2009), 5 vom: 04. Sept., Seite 1005-1018 volume:40 year:2009 number:5 day:04 month:09 pages:1005-1018 |
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Ion-exchange membrane Heterogeneous membrane Ion-exchange capacity Proton conductivity Permeability |
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Journal of applied electrochemistry |
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Bouzek, Karel @@aut@@ Moravcová, Sabina @@aut@@ Schauer, Jan @@aut@@ Brožová, Libuše @@aut@@ Pientka, Zbyněk @@aut@@ |
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Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible fluoroelastomer, rigid polystyrene (all highly hydrophobic) and hydrophilic cellulose prepared by hydrolysis of cellulose acetate butyrate. Membrane morphologies were studied by scanning electron microscopy, IR spectroscopy and density measurements. Subsequently, the membranes were characterised with respect to their swelling in water, electrochemical characteristics and transport properties. Ion-exchange capacity and proton conductivity together with the permeability to hydrogen and methanol were investigated. The important impact of the ion-exchange particles as well as of the polymer matrix used was observed. The increasing rigidity of the polymer matrix resulted in a decrease in membrane permeability, but at the same time in deterioration of its ion-exchange capacity and subsequently of the proton conductivity, too. 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Bouzek, Karel |
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Bouzek, Karel ddc 540 bkl 35.14 misc Ion-exchange membrane misc Heterogeneous membrane misc Ion-exchange capacity misc Proton conductivity misc Permeability Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties |
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540 ASE 35.14 bkl Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties Ion-exchange membrane (dpeaa)DE-He213 Heterogeneous membrane (dpeaa)DE-He213 Ion-exchange capacity (dpeaa)DE-He213 Proton conductivity (dpeaa)DE-He213 Permeability (dpeaa)DE-He213 |
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ddc 540 bkl 35.14 misc Ion-exchange membrane misc Heterogeneous membrane misc Ion-exchange capacity misc Proton conductivity misc Permeability |
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Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties |
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Bouzek, Karel Moravcová, Sabina Schauer, Jan Brožová, Libuše Pientka, Zbyněk |
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heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties |
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Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties |
| abstract |
Abstract Heterogeneous ion-exchange membranes were prepared by mixing small particles of sulfonated poly(1,4-phenylene sulfide) or sulfonated styrene–divinylbenzene copolymer with a matrix polymer. Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible fluoroelastomer, rigid polystyrene (all highly hydrophobic) and hydrophilic cellulose prepared by hydrolysis of cellulose acetate butyrate. Membrane morphologies were studied by scanning electron microscopy, IR spectroscopy and density measurements. Subsequently, the membranes were characterised with respect to their swelling in water, electrochemical characteristics and transport properties. Ion-exchange capacity and proton conductivity together with the permeability to hydrogen and methanol were investigated. The important impact of the ion-exchange particles as well as of the polymer matrix used was observed. The increasing rigidity of the polymer matrix resulted in a decrease in membrane permeability, but at the same time in deterioration of its ion-exchange capacity and subsequently of the proton conductivity, too. This was explained in terms of the limited elasticity of the polymer matrix, in each sample under study, which does not allow the ion-exchange particles to swell to an identical degree. |
| abstractGer |
Abstract Heterogeneous ion-exchange membranes were prepared by mixing small particles of sulfonated poly(1,4-phenylene sulfide) or sulfonated styrene–divinylbenzene copolymer with a matrix polymer. Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible fluoroelastomer, rigid polystyrene (all highly hydrophobic) and hydrophilic cellulose prepared by hydrolysis of cellulose acetate butyrate. Membrane morphologies were studied by scanning electron microscopy, IR spectroscopy and density measurements. Subsequently, the membranes were characterised with respect to their swelling in water, electrochemical characteristics and transport properties. Ion-exchange capacity and proton conductivity together with the permeability to hydrogen and methanol were investigated. The important impact of the ion-exchange particles as well as of the polymer matrix used was observed. The increasing rigidity of the polymer matrix resulted in a decrease in membrane permeability, but at the same time in deterioration of its ion-exchange capacity and subsequently of the proton conductivity, too. This was explained in terms of the limited elasticity of the polymer matrix, in each sample under study, which does not allow the ion-exchange particles to swell to an identical degree. |
| abstract_unstemmed |
Abstract Heterogeneous ion-exchange membranes were prepared by mixing small particles of sulfonated poly(1,4-phenylene sulfide) or sulfonated styrene–divinylbenzene copolymer with a matrix polymer. Four kinds of polymers were tested as a matrix: highly flexible linear polyethylene, medium-flexible fluoroelastomer, rigid polystyrene (all highly hydrophobic) and hydrophilic cellulose prepared by hydrolysis of cellulose acetate butyrate. Membrane morphologies were studied by scanning electron microscopy, IR spectroscopy and density measurements. Subsequently, the membranes were characterised with respect to their swelling in water, electrochemical characteristics and transport properties. Ion-exchange capacity and proton conductivity together with the permeability to hydrogen and methanol were investigated. The important impact of the ion-exchange particles as well as of the polymer matrix used was observed. The increasing rigidity of the polymer matrix resulted in a decrease in membrane permeability, but at the same time in deterioration of its ion-exchange capacity and subsequently of the proton conductivity, too. This was explained in terms of the limited elasticity of the polymer matrix, in each sample under study, which does not allow the ion-exchange particles to swell to an identical degree. |
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| title_short |
Heterogeneous ion-selective membranes: the influence of the inert matrix polymer on the membrane properties |
| url |
https://dx.doi.org/10.1007/s10800-009-9974-3 |
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| author2 |
Moravcová, Sabina Schauer, Jan Brožová, Libuše Pientka, Zbyněk |
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Moravcová, Sabina Schauer, Jan Brožová, Libuše Pientka, Zbyněk |
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| doi_str |
10.1007/s10800-009-9974-3 |
| up_date |
2024-07-03T18:48:14.075Z |
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| score |
7.402173 |