Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers
Abstract In the present work, the effect of butyl lactate methacrylate (BLM) content on the properties of acrylic acid (AA) copolymers was investigated. The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass...
Ausführliche Beschreibung
Autor*in: |
Purushothaman, M. [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2016 |
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Schlagwörter: |
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Anmerkung: |
© Pleiades Publishing, Ltd. 2016 |
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Übergeordnetes Werk: |
Enthalten in: Polymer science - Berlin : Springer, 2006, 58(2016), 3 vom: 15. Apr., Seite 368-378 |
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Übergeordnetes Werk: |
volume:58 ; year:2016 ; number:3 ; day:15 ; month:04 ; pages:368-378 |
Links: |
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DOI / URN: |
10.1134/S0965545X16030159 |
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Katalog-ID: |
SPR020246129 |
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520 | |a Abstract In the present work, the effect of butyl lactate methacrylate (BLM) content on the properties of acrylic acid (AA) copolymers was investigated. The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass spectrometric technique. Copolymers were synthesized by free-radical solution polymerization technique to obtain poly(BLM-co-AA). BLM monomer and copolymers were characterized by Fourier transform infrared (FTIR), 1H-nuclear magnetic resonance (1H-NMR) and proton decoupled 13C-NMR spectroscopic techniques. The Finemann-Ross method was used to determine the reactivity ratio of AA and BLM and the values were found to be 0.79 and 0.39, respectively. The wide angle X-ray scattering (WAXS) studies exhibited that the increase in BLM content in copolymers, shifted the amorphous halo from 21.34° to 15.39° and also increased the average molecular interchain spacing (〈R〉) from 5.20 to 7.18 Å, which was calculated from 2θ values of amorphous halo of copolymers. Moisture absorption of polymers followed Fickian absorption. Depending upon the copolymer composition, relative humidity and time, the moisture absorption of copolymers can be tuned to a wide range from 11 to 35% (wt/wt). Glass transition temperature of copolymers decreased from 106 to 72.1°C with increase in BLM content. Copolymers were thermally stable up to 150°C and thereafter exhibited three-step thermal degradation in nitrogen atmosphere. Thermal stability of copolymers can be explained on the basis of 〈R〉 value. | ||
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650 | 4 | |a Methacrylic Acid |7 (dpeaa)DE-He213 | |
650 | 4 | |a Moisture Absorption |7 (dpeaa)DE-He213 | |
650 | 4 | |a Copolymer Composition |7 (dpeaa)DE-He213 | |
650 | 4 | |a Differential Scanning Calorimeter Curve |7 (dpeaa)DE-He213 | |
700 | 1 | |a Krishnan, P. Santhana Gopala |4 aut | |
700 | 1 | |a Nayak, S. K. |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Polymer science |d Berlin : Springer, 2006 |g 58(2016), 3 vom: 15. Apr., Seite 368-378 |w (DE-627)509758509 |w (DE-600)2228442-4 |x 1555-6107 |7 nnns |
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10.1134/S0965545X16030159 doi (DE-627)SPR020246129 (SPR)S0965545X16030159-e DE-627 ger DE-627 rakwb eng Purushothaman, M. verfasserin aut Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2016 Abstract In the present work, the effect of butyl lactate methacrylate (BLM) content on the properties of acrylic acid (AA) copolymers was investigated. The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass spectrometric technique. Copolymers were synthesized by free-radical solution polymerization technique to obtain poly(BLM-co-AA). BLM monomer and copolymers were characterized by Fourier transform infrared (FTIR), 1H-nuclear magnetic resonance (1H-NMR) and proton decoupled 13C-NMR spectroscopic techniques. The Finemann-Ross method was used to determine the reactivity ratio of AA and BLM and the values were found to be 0.79 and 0.39, respectively. The wide angle X-ray scattering (WAXS) studies exhibited that the increase in BLM content in copolymers, shifted the amorphous halo from 21.34° to 15.39° and also increased the average molecular interchain spacing (〈R〉) from 5.20 to 7.18 Å, which was calculated from 2θ values of amorphous halo of copolymers. Moisture absorption of polymers followed Fickian absorption. Depending upon the copolymer composition, relative humidity and time, the moisture absorption of copolymers can be tuned to a wide range from 11 to 35% (wt/wt). Glass transition temperature of copolymers decreased from 106 to 72.1°C with increase in BLM content. Copolymers were thermally stable up to 150°C and thereafter exhibited three-step thermal degradation in nitrogen atmosphere. Thermal stability of copolymers can be explained on the basis of 〈R〉 value. Acrylic Acid (dpeaa)DE-He213 Methacrylic Acid (dpeaa)DE-He213 Moisture Absorption (dpeaa)DE-He213 Copolymer Composition (dpeaa)DE-He213 Differential Scanning Calorimeter Curve (dpeaa)DE-He213 Krishnan, P. Santhana Gopala aut Nayak, S. K. aut Enthalten in Polymer science Berlin : Springer, 2006 58(2016), 3 vom: 15. Apr., Seite 368-378 (DE-627)509758509 (DE-600)2228442-4 1555-6107 nnns volume:58 year:2016 number:3 day:15 month:04 pages:368-378 https://dx.doi.org/10.1134/S0965545X16030159 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_65 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_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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 AR 58 2016 3 15 04 368-378 |
spelling |
10.1134/S0965545X16030159 doi (DE-627)SPR020246129 (SPR)S0965545X16030159-e DE-627 ger DE-627 rakwb eng Purushothaman, M. verfasserin aut Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2016 Abstract In the present work, the effect of butyl lactate methacrylate (BLM) content on the properties of acrylic acid (AA) copolymers was investigated. The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass spectrometric technique. Copolymers were synthesized by free-radical solution polymerization technique to obtain poly(BLM-co-AA). BLM monomer and copolymers were characterized by Fourier transform infrared (FTIR), 1H-nuclear magnetic resonance (1H-NMR) and proton decoupled 13C-NMR spectroscopic techniques. The Finemann-Ross method was used to determine the reactivity ratio of AA and BLM and the values were found to be 0.79 and 0.39, respectively. The wide angle X-ray scattering (WAXS) studies exhibited that the increase in BLM content in copolymers, shifted the amorphous halo from 21.34° to 15.39° and also increased the average molecular interchain spacing (〈R〉) from 5.20 to 7.18 Å, which was calculated from 2θ values of amorphous halo of copolymers. Moisture absorption of polymers followed Fickian absorption. Depending upon the copolymer composition, relative humidity and time, the moisture absorption of copolymers can be tuned to a wide range from 11 to 35% (wt/wt). Glass transition temperature of copolymers decreased from 106 to 72.1°C with increase in BLM content. Copolymers were thermally stable up to 150°C and thereafter exhibited three-step thermal degradation in nitrogen atmosphere. Thermal stability of copolymers can be explained on the basis of 〈R〉 value. Acrylic Acid (dpeaa)DE-He213 Methacrylic Acid (dpeaa)DE-He213 Moisture Absorption (dpeaa)DE-He213 Copolymer Composition (dpeaa)DE-He213 Differential Scanning Calorimeter Curve (dpeaa)DE-He213 Krishnan, P. Santhana Gopala aut Nayak, S. K. aut Enthalten in Polymer science Berlin : Springer, 2006 58(2016), 3 vom: 15. Apr., Seite 368-378 (DE-627)509758509 (DE-600)2228442-4 1555-6107 nnns volume:58 year:2016 number:3 day:15 month:04 pages:368-378 https://dx.doi.org/10.1134/S0965545X16030159 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_65 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_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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 AR 58 2016 3 15 04 368-378 |
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10.1134/S0965545X16030159 doi (DE-627)SPR020246129 (SPR)S0965545X16030159-e DE-627 ger DE-627 rakwb eng Purushothaman, M. verfasserin aut Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2016 Abstract In the present work, the effect of butyl lactate methacrylate (BLM) content on the properties of acrylic acid (AA) copolymers was investigated. The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass spectrometric technique. Copolymers were synthesized by free-radical solution polymerization technique to obtain poly(BLM-co-AA). BLM monomer and copolymers were characterized by Fourier transform infrared (FTIR), 1H-nuclear magnetic resonance (1H-NMR) and proton decoupled 13C-NMR spectroscopic techniques. The Finemann-Ross method was used to determine the reactivity ratio of AA and BLM and the values were found to be 0.79 and 0.39, respectively. The wide angle X-ray scattering (WAXS) studies exhibited that the increase in BLM content in copolymers, shifted the amorphous halo from 21.34° to 15.39° and also increased the average molecular interchain spacing (〈R〉) from 5.20 to 7.18 Å, which was calculated from 2θ values of amorphous halo of copolymers. Moisture absorption of polymers followed Fickian absorption. Depending upon the copolymer composition, relative humidity and time, the moisture absorption of copolymers can be tuned to a wide range from 11 to 35% (wt/wt). Glass transition temperature of copolymers decreased from 106 to 72.1°C with increase in BLM content. Copolymers were thermally stable up to 150°C and thereafter exhibited three-step thermal degradation in nitrogen atmosphere. Thermal stability of copolymers can be explained on the basis of 〈R〉 value. Acrylic Acid (dpeaa)DE-He213 Methacrylic Acid (dpeaa)DE-He213 Moisture Absorption (dpeaa)DE-He213 Copolymer Composition (dpeaa)DE-He213 Differential Scanning Calorimeter Curve (dpeaa)DE-He213 Krishnan, P. Santhana Gopala aut Nayak, S. K. aut Enthalten in Polymer science Berlin : Springer, 2006 58(2016), 3 vom: 15. Apr., Seite 368-378 (DE-627)509758509 (DE-600)2228442-4 1555-6107 nnns volume:58 year:2016 number:3 day:15 month:04 pages:368-378 https://dx.doi.org/10.1134/S0965545X16030159 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_65 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_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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 AR 58 2016 3 15 04 368-378 |
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10.1134/S0965545X16030159 doi (DE-627)SPR020246129 (SPR)S0965545X16030159-e DE-627 ger DE-627 rakwb eng Purushothaman, M. verfasserin aut Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2016 Abstract In the present work, the effect of butyl lactate methacrylate (BLM) content on the properties of acrylic acid (AA) copolymers was investigated. The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass spectrometric technique. Copolymers were synthesized by free-radical solution polymerization technique to obtain poly(BLM-co-AA). BLM monomer and copolymers were characterized by Fourier transform infrared (FTIR), 1H-nuclear magnetic resonance (1H-NMR) and proton decoupled 13C-NMR spectroscopic techniques. The Finemann-Ross method was used to determine the reactivity ratio of AA and BLM and the values were found to be 0.79 and 0.39, respectively. The wide angle X-ray scattering (WAXS) studies exhibited that the increase in BLM content in copolymers, shifted the amorphous halo from 21.34° to 15.39° and also increased the average molecular interchain spacing (〈R〉) from 5.20 to 7.18 Å, which was calculated from 2θ values of amorphous halo of copolymers. Moisture absorption of polymers followed Fickian absorption. Depending upon the copolymer composition, relative humidity and time, the moisture absorption of copolymers can be tuned to a wide range from 11 to 35% (wt/wt). Glass transition temperature of copolymers decreased from 106 to 72.1°C with increase in BLM content. Copolymers were thermally stable up to 150°C and thereafter exhibited three-step thermal degradation in nitrogen atmosphere. Thermal stability of copolymers can be explained on the basis of 〈R〉 value. Acrylic Acid (dpeaa)DE-He213 Methacrylic Acid (dpeaa)DE-He213 Moisture Absorption (dpeaa)DE-He213 Copolymer Composition (dpeaa)DE-He213 Differential Scanning Calorimeter Curve (dpeaa)DE-He213 Krishnan, P. Santhana Gopala aut Nayak, S. K. aut Enthalten in Polymer science Berlin : Springer, 2006 58(2016), 3 vom: 15. Apr., Seite 368-378 (DE-627)509758509 (DE-600)2228442-4 1555-6107 nnns volume:58 year:2016 number:3 day:15 month:04 pages:368-378 https://dx.doi.org/10.1134/S0965545X16030159 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_65 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_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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 AR 58 2016 3 15 04 368-378 |
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10.1134/S0965545X16030159 doi (DE-627)SPR020246129 (SPR)S0965545X16030159-e DE-627 ger DE-627 rakwb eng Purushothaman, M. verfasserin aut Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers 2016 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2016 Abstract In the present work, the effect of butyl lactate methacrylate (BLM) content on the properties of acrylic acid (AA) copolymers was investigated. The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass spectrometric technique. Copolymers were synthesized by free-radical solution polymerization technique to obtain poly(BLM-co-AA). BLM monomer and copolymers were characterized by Fourier transform infrared (FTIR), 1H-nuclear magnetic resonance (1H-NMR) and proton decoupled 13C-NMR spectroscopic techniques. The Finemann-Ross method was used to determine the reactivity ratio of AA and BLM and the values were found to be 0.79 and 0.39, respectively. The wide angle X-ray scattering (WAXS) studies exhibited that the increase in BLM content in copolymers, shifted the amorphous halo from 21.34° to 15.39° and also increased the average molecular interchain spacing (〈R〉) from 5.20 to 7.18 Å, which was calculated from 2θ values of amorphous halo of copolymers. Moisture absorption of polymers followed Fickian absorption. Depending upon the copolymer composition, relative humidity and time, the moisture absorption of copolymers can be tuned to a wide range from 11 to 35% (wt/wt). Glass transition temperature of copolymers decreased from 106 to 72.1°C with increase in BLM content. Copolymers were thermally stable up to 150°C and thereafter exhibited three-step thermal degradation in nitrogen atmosphere. Thermal stability of copolymers can be explained on the basis of 〈R〉 value. Acrylic Acid (dpeaa)DE-He213 Methacrylic Acid (dpeaa)DE-He213 Moisture Absorption (dpeaa)DE-He213 Copolymer Composition (dpeaa)DE-He213 Differential Scanning Calorimeter Curve (dpeaa)DE-He213 Krishnan, P. Santhana Gopala aut Nayak, S. K. aut Enthalten in Polymer science Berlin : Springer, 2006 58(2016), 3 vom: 15. Apr., Seite 368-378 (DE-627)509758509 (DE-600)2228442-4 1555-6107 nnns volume:58 year:2016 number:3 day:15 month:04 pages:368-378 https://dx.doi.org/10.1134/S0965545X16030159 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_65 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_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_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_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 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 AR 58 2016 3 15 04 368-378 |
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Enthalten in Polymer science 58(2016), 3 vom: 15. Apr., Seite 368-378 volume:58 year:2016 number:3 day:15 month:04 pages:368-378 |
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The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass spectrometric technique. Copolymers were synthesized by free-radical solution polymerization technique to obtain poly(BLM-co-AA). BLM monomer and copolymers were characterized by Fourier transform infrared (FTIR), 1H-nuclear magnetic resonance (1H-NMR) and proton decoupled 13C-NMR spectroscopic techniques. The Finemann-Ross method was used to determine the reactivity ratio of AA and BLM and the values were found to be 0.79 and 0.39, respectively. The wide angle X-ray scattering (WAXS) studies exhibited that the increase in BLM content in copolymers, shifted the amorphous halo from 21.34° to 15.39° and also increased the average molecular interchain spacing (〈R〉) from 5.20 to 7.18 Å, which was calculated from 2θ values of amorphous halo of copolymers. Moisture absorption of polymers followed Fickian absorption. Depending upon the copolymer composition, relative humidity and time, the moisture absorption of copolymers can be tuned to a wide range from 11 to 35% (wt/wt). Glass transition temperature of copolymers decreased from 106 to 72.1°C with increase in BLM content. Copolymers were thermally stable up to 150°C and thereafter exhibited three-step thermal degradation in nitrogen atmosphere. 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Purushothaman, M. |
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Purushothaman, M. misc Acrylic Acid misc Methacrylic Acid misc Moisture Absorption misc Copolymer Composition misc Differential Scanning Calorimeter Curve Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers |
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Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers Acrylic Acid (dpeaa)DE-He213 Methacrylic Acid (dpeaa)DE-He213 Moisture Absorption (dpeaa)DE-He213 Copolymer Composition (dpeaa)DE-He213 Differential Scanning Calorimeter Curve (dpeaa)DE-He213 |
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Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers |
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Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers |
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effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers |
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Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers |
abstract |
Abstract In the present work, the effect of butyl lactate methacrylate (BLM) content on the properties of acrylic acid (AA) copolymers was investigated. The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass spectrometric technique. Copolymers were synthesized by free-radical solution polymerization technique to obtain poly(BLM-co-AA). BLM monomer and copolymers were characterized by Fourier transform infrared (FTIR), 1H-nuclear magnetic resonance (1H-NMR) and proton decoupled 13C-NMR spectroscopic techniques. The Finemann-Ross method was used to determine the reactivity ratio of AA and BLM and the values were found to be 0.79 and 0.39, respectively. The wide angle X-ray scattering (WAXS) studies exhibited that the increase in BLM content in copolymers, shifted the amorphous halo from 21.34° to 15.39° and also increased the average molecular interchain spacing (〈R〉) from 5.20 to 7.18 Å, which was calculated from 2θ values of amorphous halo of copolymers. Moisture absorption of polymers followed Fickian absorption. Depending upon the copolymer composition, relative humidity and time, the moisture absorption of copolymers can be tuned to a wide range from 11 to 35% (wt/wt). Glass transition temperature of copolymers decreased from 106 to 72.1°C with increase in BLM content. Copolymers were thermally stable up to 150°C and thereafter exhibited three-step thermal degradation in nitrogen atmosphere. Thermal stability of copolymers can be explained on the basis of 〈R〉 value. © Pleiades Publishing, Ltd. 2016 |
abstractGer |
Abstract In the present work, the effect of butyl lactate methacrylate (BLM) content on the properties of acrylic acid (AA) copolymers was investigated. The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass spectrometric technique. Copolymers were synthesized by free-radical solution polymerization technique to obtain poly(BLM-co-AA). BLM monomer and copolymers were characterized by Fourier transform infrared (FTIR), 1H-nuclear magnetic resonance (1H-NMR) and proton decoupled 13C-NMR spectroscopic techniques. The Finemann-Ross method was used to determine the reactivity ratio of AA and BLM and the values were found to be 0.79 and 0.39, respectively. The wide angle X-ray scattering (WAXS) studies exhibited that the increase in BLM content in copolymers, shifted the amorphous halo from 21.34° to 15.39° and also increased the average molecular interchain spacing (〈R〉) from 5.20 to 7.18 Å, which was calculated from 2θ values of amorphous halo of copolymers. Moisture absorption of polymers followed Fickian absorption. Depending upon the copolymer composition, relative humidity and time, the moisture absorption of copolymers can be tuned to a wide range from 11 to 35% (wt/wt). Glass transition temperature of copolymers decreased from 106 to 72.1°C with increase in BLM content. Copolymers were thermally stable up to 150°C and thereafter exhibited three-step thermal degradation in nitrogen atmosphere. Thermal stability of copolymers can be explained on the basis of 〈R〉 value. © Pleiades Publishing, Ltd. 2016 |
abstract_unstemmed |
Abstract In the present work, the effect of butyl lactate methacrylate (BLM) content on the properties of acrylic acid (AA) copolymers was investigated. The BLM monomer was synthesized by reacting butyl lactate with methacrylic acid through azeotropic distillation method, which was confirmed by Mass spectrometric technique. Copolymers were synthesized by free-radical solution polymerization technique to obtain poly(BLM-co-AA). BLM monomer and copolymers were characterized by Fourier transform infrared (FTIR), 1H-nuclear magnetic resonance (1H-NMR) and proton decoupled 13C-NMR spectroscopic techniques. The Finemann-Ross method was used to determine the reactivity ratio of AA and BLM and the values were found to be 0.79 and 0.39, respectively. The wide angle X-ray scattering (WAXS) studies exhibited that the increase in BLM content in copolymers, shifted the amorphous halo from 21.34° to 15.39° and also increased the average molecular interchain spacing (〈R〉) from 5.20 to 7.18 Å, which was calculated from 2θ values of amorphous halo of copolymers. Moisture absorption of polymers followed Fickian absorption. Depending upon the copolymer composition, relative humidity and time, the moisture absorption of copolymers can be tuned to a wide range from 11 to 35% (wt/wt). Glass transition temperature of copolymers decreased from 106 to 72.1°C with increase in BLM content. Copolymers were thermally stable up to 150°C and thereafter exhibited three-step thermal degradation in nitrogen atmosphere. Thermal stability of copolymers can be explained on the basis of 〈R〉 value. © Pleiades Publishing, Ltd. 2016 |
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container_issue |
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title_short |
Effect of butyl lactate methacrylate content on the properties of acrylic acid copolymers |
url |
https://dx.doi.org/10.1134/S0965545X16030159 |
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author2 |
Krishnan, P. Santhana Gopala Nayak, S. K. |
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Krishnan, P. Santhana Gopala Nayak, S. K. |
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10.1134/S0965545X16030159 |
up_date |
2024-07-03T14:50:21.035Z |
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score |
7.3982153 |