Synthesis of rubber seed oil waterborne alkyd resin from glucitol

Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride,...
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Autor*in:	Uzoh, C. F. [verfasserIn] Obele, M. C. [verfasserIn] Umennabuife, U. M. [verfasserIn] Onukwuli, O. D. [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2019

Schlagwörter:	Glucitol Polymerization Alkyd resin Solubility

Übergeordnetes Werk:	Enthalten in: Journal of coatings technology and research - Blue Bell, Pa., 2004, 16(2019), 6 vom: 21. Juni, Seite 1727-1735
Übergeordnetes Werk:	volume:16 ; year:2019 ; number:6 ; day:21 ; month:06 ; pages:1727-1735

Links:	Volltext

DOI / URN:	10.1007/s11998-019-00235-0

Katalog-ID:	SPR02362180X

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520			\|a Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride, maleic anhydride, glucitol aqueous solution, and RSO. The physical, chemical, and film characteristics of the glucitol-modified alkyd resins were examined, and the result was compared with the standard alkyd resins and soybean-based alkyd resin. It was observed that all samples were soluble in xylene and butoxyethanol but not water. All of the samples have varying solubilities in water/xylene ratio (%) and complete solubility in water/butoxyethanol (%) ratio of 40:60, 50:50, and 60:40, respectively. ALKYD A is soluble in all solvents except water where it was sparingly soluble at room temperature. The spectral analysis revealed the polyesterification reaction and hydrogen-bonding integrity of the alkyd resins and the polybasic acid. The physical and chemical properties and the performance indices of the glucitol-based alkyd resin results show that they possess acceptable drying properties, chemical resistance, and mechanical properties. Performance of ALKYD A and C gave nearly the same result as the standard alkyd resins and soybean-based alkyd resin. It has potential as a choice waterborne binder for alkyd resin paint and can help in reducing VOC.
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allfields	10.1007/s11998-019-00235-0 doi (DE-627)SPR02362180X (SPR)s11998-019-00235-0-e DE-627 ger DE-627 rakwb eng 600 ASE Uzoh, C. F. verfasserin aut Synthesis of rubber seed oil waterborne alkyd resin from glucitol 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride, maleic anhydride, glucitol aqueous solution, and RSO. The physical, chemical, and film characteristics of the glucitol-modified alkyd resins were examined, and the result was compared with the standard alkyd resins and soybean-based alkyd resin. It was observed that all samples were soluble in xylene and butoxyethanol but not water. All of the samples have varying solubilities in water/xylene ratio (%) and complete solubility in water/butoxyethanol (%) ratio of 40:60, 50:50, and 60:40, respectively. ALKYD A is soluble in all solvents except water where it was sparingly soluble at room temperature. The spectral analysis revealed the polyesterification reaction and hydrogen-bonding integrity of the alkyd resins and the polybasic acid. The physical and chemical properties and the performance indices of the glucitol-based alkyd resin results show that they possess acceptable drying properties, chemical resistance, and mechanical properties. Performance of ALKYD A and C gave nearly the same result as the standard alkyd resins and soybean-based alkyd resin. It has potential as a choice waterborne binder for alkyd resin paint and can help in reducing VOC. Glucitol (dpeaa)DE-He213 Polymerization (dpeaa)DE-He213 Alkyd resin (dpeaa)DE-He213 Solubility (dpeaa)DE-He213 Obele, M. C. verfasserin aut Umennabuife, U. M. verfasserin aut Onukwuli, O. D. verfasserin aut Enthalten in Journal of coatings technology and research Blue Bell, Pa., 2004 16(2019), 6 vom: 21. Juni, Seite 1727-1735 (DE-627)51834584X (DE-600)2252471-X 1935-3804 nnns volume:16 year:2019 number:6 day:21 month:06 pages:1727-1735 https://dx.doi.org/10.1007/s11998-019-00235-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 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_266 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 16 2019 6 21 06 1727-1735
spelling	10.1007/s11998-019-00235-0 doi (DE-627)SPR02362180X (SPR)s11998-019-00235-0-e DE-627 ger DE-627 rakwb eng 600 ASE Uzoh, C. F. verfasserin aut Synthesis of rubber seed oil waterborne alkyd resin from glucitol 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride, maleic anhydride, glucitol aqueous solution, and RSO. The physical, chemical, and film characteristics of the glucitol-modified alkyd resins were examined, and the result was compared with the standard alkyd resins and soybean-based alkyd resin. It was observed that all samples were soluble in xylene and butoxyethanol but not water. All of the samples have varying solubilities in water/xylene ratio (%) and complete solubility in water/butoxyethanol (%) ratio of 40:60, 50:50, and 60:40, respectively. ALKYD A is soluble in all solvents except water where it was sparingly soluble at room temperature. The spectral analysis revealed the polyesterification reaction and hydrogen-bonding integrity of the alkyd resins and the polybasic acid. The physical and chemical properties and the performance indices of the glucitol-based alkyd resin results show that they possess acceptable drying properties, chemical resistance, and mechanical properties. Performance of ALKYD A and C gave nearly the same result as the standard alkyd resins and soybean-based alkyd resin. It has potential as a choice waterborne binder for alkyd resin paint and can help in reducing VOC. Glucitol (dpeaa)DE-He213 Polymerization (dpeaa)DE-He213 Alkyd resin (dpeaa)DE-He213 Solubility (dpeaa)DE-He213 Obele, M. C. verfasserin aut Umennabuife, U. M. verfasserin aut Onukwuli, O. D. verfasserin aut Enthalten in Journal of coatings technology and research Blue Bell, Pa., 2004 16(2019), 6 vom: 21. Juni, Seite 1727-1735 (DE-627)51834584X (DE-600)2252471-X 1935-3804 nnns volume:16 year:2019 number:6 day:21 month:06 pages:1727-1735 https://dx.doi.org/10.1007/s11998-019-00235-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 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_266 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 16 2019 6 21 06 1727-1735
allfields_unstemmed	10.1007/s11998-019-00235-0 doi (DE-627)SPR02362180X (SPR)s11998-019-00235-0-e DE-627 ger DE-627 rakwb eng 600 ASE Uzoh, C. F. verfasserin aut Synthesis of rubber seed oil waterborne alkyd resin from glucitol 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride, maleic anhydride, glucitol aqueous solution, and RSO. The physical, chemical, and film characteristics of the glucitol-modified alkyd resins were examined, and the result was compared with the standard alkyd resins and soybean-based alkyd resin. It was observed that all samples were soluble in xylene and butoxyethanol but not water. All of the samples have varying solubilities in water/xylene ratio (%) and complete solubility in water/butoxyethanol (%) ratio of 40:60, 50:50, and 60:40, respectively. ALKYD A is soluble in all solvents except water where it was sparingly soluble at room temperature. The spectral analysis revealed the polyesterification reaction and hydrogen-bonding integrity of the alkyd resins and the polybasic acid. The physical and chemical properties and the performance indices of the glucitol-based alkyd resin results show that they possess acceptable drying properties, chemical resistance, and mechanical properties. Performance of ALKYD A and C gave nearly the same result as the standard alkyd resins and soybean-based alkyd resin. It has potential as a choice waterborne binder for alkyd resin paint and can help in reducing VOC. Glucitol (dpeaa)DE-He213 Polymerization (dpeaa)DE-He213 Alkyd resin (dpeaa)DE-He213 Solubility (dpeaa)DE-He213 Obele, M. C. verfasserin aut Umennabuife, U. M. verfasserin aut Onukwuli, O. D. verfasserin aut Enthalten in Journal of coatings technology and research Blue Bell, Pa., 2004 16(2019), 6 vom: 21. Juni, Seite 1727-1735 (DE-627)51834584X (DE-600)2252471-X 1935-3804 nnns volume:16 year:2019 number:6 day:21 month:06 pages:1727-1735 https://dx.doi.org/10.1007/s11998-019-00235-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 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_266 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 16 2019 6 21 06 1727-1735
allfieldsGer	10.1007/s11998-019-00235-0 doi (DE-627)SPR02362180X (SPR)s11998-019-00235-0-e DE-627 ger DE-627 rakwb eng 600 ASE Uzoh, C. F. verfasserin aut Synthesis of rubber seed oil waterborne alkyd resin from glucitol 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride, maleic anhydride, glucitol aqueous solution, and RSO. The physical, chemical, and film characteristics of the glucitol-modified alkyd resins were examined, and the result was compared with the standard alkyd resins and soybean-based alkyd resin. It was observed that all samples were soluble in xylene and butoxyethanol but not water. All of the samples have varying solubilities in water/xylene ratio (%) and complete solubility in water/butoxyethanol (%) ratio of 40:60, 50:50, and 60:40, respectively. ALKYD A is soluble in all solvents except water where it was sparingly soluble at room temperature. The spectral analysis revealed the polyesterification reaction and hydrogen-bonding integrity of the alkyd resins and the polybasic acid. The physical and chemical properties and the performance indices of the glucitol-based alkyd resin results show that they possess acceptable drying properties, chemical resistance, and mechanical properties. Performance of ALKYD A and C gave nearly the same result as the standard alkyd resins and soybean-based alkyd resin. It has potential as a choice waterborne binder for alkyd resin paint and can help in reducing VOC. Glucitol (dpeaa)DE-He213 Polymerization (dpeaa)DE-He213 Alkyd resin (dpeaa)DE-He213 Solubility (dpeaa)DE-He213 Obele, M. C. verfasserin aut Umennabuife, U. M. verfasserin aut Onukwuli, O. D. verfasserin aut Enthalten in Journal of coatings technology and research Blue Bell, Pa., 2004 16(2019), 6 vom: 21. Juni, Seite 1727-1735 (DE-627)51834584X (DE-600)2252471-X 1935-3804 nnns volume:16 year:2019 number:6 day:21 month:06 pages:1727-1735 https://dx.doi.org/10.1007/s11998-019-00235-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 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_266 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 16 2019 6 21 06 1727-1735
allfieldsSound	10.1007/s11998-019-00235-0 doi (DE-627)SPR02362180X (SPR)s11998-019-00235-0-e DE-627 ger DE-627 rakwb eng 600 ASE Uzoh, C. F. verfasserin aut Synthesis of rubber seed oil waterborne alkyd resin from glucitol 2019 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride, maleic anhydride, glucitol aqueous solution, and RSO. The physical, chemical, and film characteristics of the glucitol-modified alkyd resins were examined, and the result was compared with the standard alkyd resins and soybean-based alkyd resin. It was observed that all samples were soluble in xylene and butoxyethanol but not water. All of the samples have varying solubilities in water/xylene ratio (%) and complete solubility in water/butoxyethanol (%) ratio of 40:60, 50:50, and 60:40, respectively. ALKYD A is soluble in all solvents except water where it was sparingly soluble at room temperature. The spectral analysis revealed the polyesterification reaction and hydrogen-bonding integrity of the alkyd resins and the polybasic acid. The physical and chemical properties and the performance indices of the glucitol-based alkyd resin results show that they possess acceptable drying properties, chemical resistance, and mechanical properties. Performance of ALKYD A and C gave nearly the same result as the standard alkyd resins and soybean-based alkyd resin. It has potential as a choice waterborne binder for alkyd resin paint and can help in reducing VOC. Glucitol (dpeaa)DE-He213 Polymerization (dpeaa)DE-He213 Alkyd resin (dpeaa)DE-He213 Solubility (dpeaa)DE-He213 Obele, M. C. verfasserin aut Umennabuife, U. M. verfasserin aut Onukwuli, O. D. verfasserin aut Enthalten in Journal of coatings technology and research Blue Bell, Pa., 2004 16(2019), 6 vom: 21. Juni, Seite 1727-1735 (DE-627)51834584X (DE-600)2252471-X 1935-3804 nnns volume:16 year:2019 number:6 day:21 month:06 pages:1727-1735 https://dx.doi.org/10.1007/s11998-019-00235-0 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER 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_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 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_266 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 16 2019 6 21 06 1727-1735
language	English
source	Enthalten in Journal of coatings technology and research 16(2019), 6 vom: 21. Juni, Seite 1727-1735 volume:16 year:2019 number:6 day:21 month:06 pages:1727-1735
sourceStr	Enthalten in Journal of coatings technology and research 16(2019), 6 vom: 21. Juni, Seite 1727-1735 volume:16 year:2019 number:6 day:21 month:06 pages:1727-1735
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Glucitol Polymerization Alkyd resin Solubility
dewey-raw	600
isfreeaccess_bool	false
container_title	Journal of coatings technology and research
authorswithroles_txt_mv	Uzoh, C. F. @@aut@@ Obele, M. C. @@aut@@ Umennabuife, U. M. @@aut@@ Onukwuli, O. D. @@aut@@
publishDateDaySort_date	2019-06-21T00:00:00Z
hierarchy_top_id	51834584X
dewey-sort	3600
id	SPR02362180X
language_de	englisch
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author	Uzoh, C. F.
spellingShingle	Uzoh, C. F. ddc 600 misc Glucitol misc Polymerization misc Alkyd resin misc Solubility Synthesis of rubber seed oil waterborne alkyd resin from glucitol
authorStr	Uzoh, C. F.
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topic_title	600 ASE Synthesis of rubber seed oil waterborne alkyd resin from glucitol Glucitol (dpeaa)DE-He213 Polymerization (dpeaa)DE-He213 Alkyd resin (dpeaa)DE-He213 Solubility (dpeaa)DE-He213
topic	ddc 600 misc Glucitol misc Polymerization misc Alkyd resin misc Solubility
topic_unstemmed	ddc 600 misc Glucitol misc Polymerization misc Alkyd resin misc Solubility
topic_browse	ddc 600 misc Glucitol misc Polymerization misc Alkyd resin misc Solubility
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title	Synthesis of rubber seed oil waterborne alkyd resin from glucitol
ctrlnum	(DE-627)SPR02362180X (SPR)s11998-019-00235-0-e
title_full	Synthesis of rubber seed oil waterborne alkyd resin from glucitol
author_sort	Uzoh, C. F.
journal	Journal of coatings technology and research
journalStr	Journal of coatings technology and research
lang_code	eng
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container_start_page	1727
author_browse	Uzoh, C. F. Obele, M. C. Umennabuife, U. M. Onukwuli, O. D.
container_volume	16
class	600 ASE
format_se	Elektronische Aufsätze
author-letter	Uzoh, C. F.
doi_str_mv	10.1007/s11998-019-00235-0
dewey-full	600
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title_sort	synthesis of rubber seed oil waterborne alkyd resin from glucitol
title_auth	Synthesis of rubber seed oil waterborne alkyd resin from glucitol
abstract	Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride, maleic anhydride, glucitol aqueous solution, and RSO. The physical, chemical, and film characteristics of the glucitol-modified alkyd resins were examined, and the result was compared with the standard alkyd resins and soybean-based alkyd resin. It was observed that all samples were soluble in xylene and butoxyethanol but not water. All of the samples have varying solubilities in water/xylene ratio (%) and complete solubility in water/butoxyethanol (%) ratio of 40:60, 50:50, and 60:40, respectively. ALKYD A is soluble in all solvents except water where it was sparingly soluble at room temperature. The spectral analysis revealed the polyesterification reaction and hydrogen-bonding integrity of the alkyd resins and the polybasic acid. The physical and chemical properties and the performance indices of the glucitol-based alkyd resin results show that they possess acceptable drying properties, chemical resistance, and mechanical properties. Performance of ALKYD A and C gave nearly the same result as the standard alkyd resins and soybean-based alkyd resin. It has potential as a choice waterborne binder for alkyd resin paint and can help in reducing VOC.
abstractGer	Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride, maleic anhydride, glucitol aqueous solution, and RSO. The physical, chemical, and film characteristics of the glucitol-modified alkyd resins were examined, and the result was compared with the standard alkyd resins and soybean-based alkyd resin. It was observed that all samples were soluble in xylene and butoxyethanol but not water. All of the samples have varying solubilities in water/xylene ratio (%) and complete solubility in water/butoxyethanol (%) ratio of 40:60, 50:50, and 60:40, respectively. ALKYD A is soluble in all solvents except water where it was sparingly soluble at room temperature. The spectral analysis revealed the polyesterification reaction and hydrogen-bonding integrity of the alkyd resins and the polybasic acid. The physical and chemical properties and the performance indices of the glucitol-based alkyd resin results show that they possess acceptable drying properties, chemical resistance, and mechanical properties. Performance of ALKYD A and C gave nearly the same result as the standard alkyd resins and soybean-based alkyd resin. It has potential as a choice waterborne binder for alkyd resin paint and can help in reducing VOC.
abstract_unstemmed	Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride, maleic anhydride, glucitol aqueous solution, and RSO. The physical, chemical, and film characteristics of the glucitol-modified alkyd resins were examined, and the result was compared with the standard alkyd resins and soybean-based alkyd resin. It was observed that all samples were soluble in xylene and butoxyethanol but not water. All of the samples have varying solubilities in water/xylene ratio (%) and complete solubility in water/butoxyethanol (%) ratio of 40:60, 50:50, and 60:40, respectively. ALKYD A is soluble in all solvents except water where it was sparingly soluble at room temperature. The spectral analysis revealed the polyesterification reaction and hydrogen-bonding integrity of the alkyd resins and the polybasic acid. The physical and chemical properties and the performance indices of the glucitol-based alkyd resin results show that they possess acceptable drying properties, chemical resistance, and mechanical properties. Performance of ALKYD A and C gave nearly the same result as the standard alkyd resins and soybean-based alkyd resin. It has potential as a choice waterborne binder for alkyd resin paint and can help in reducing VOC.
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container_issue	6
title_short	Synthesis of rubber seed oil waterborne alkyd resin from glucitol
url	https://dx.doi.org/10.1007/s11998-019-00235-0
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author2	Obele, M. C. Umennabuife, U. M. Onukwuli, O. D.
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doi_str	10.1007/s11998-019-00235-0
up_date	2024-07-03T20:09:49.164Z
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fullrecord_marcxml	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR02362180X</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20220111103109.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201006s2019 xx \|\|\|\|\|o 00\| \|\|eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s11998-019-00235-0</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR02362180X</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s11998-019-00235-0-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">600</subfield><subfield code="q">ASE</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Uzoh, C. F.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Synthesis of rubber seed oil waterborne alkyd resin from glucitol</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2019</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Solubility properties of alkyd resins from phthalic and maleic anhydrides, glucitol and rubber seed oil (RSO) as raw materials were examined. Four types of glucitol-based medium oil length alkyd resins (ALKYD A–D, two for each acid anhydride) samples were formulated with phthalic anhydride, maleic anhydride, glucitol aqueous solution, and RSO. The physical, chemical, and film characteristics of the glucitol-modified alkyd resins were examined, and the result was compared with the standard alkyd resins and soybean-based alkyd resin. It was observed that all samples were soluble in xylene and butoxyethanol but not water. All of the samples have varying solubilities in water/xylene ratio (%) and complete solubility in water/butoxyethanol (%) ratio of 40:60, 50:50, and 60:40, respectively. ALKYD A is soluble in all solvents except water where it was sparingly soluble at room temperature. The spectral analysis revealed the polyesterification reaction and hydrogen-bonding integrity of the alkyd resins and the polybasic acid. The physical and chemical properties and the performance indices of the glucitol-based alkyd resin results show that they possess acceptable drying properties, chemical resistance, and mechanical properties. Performance of ALKYD A and C gave nearly the same result as the standard alkyd resins and soybean-based alkyd resin. It has potential as a choice waterborne binder for alkyd resin paint and can help in reducing VOC.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Glucitol</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Polymerization</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Alkyd resin</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Solubility</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Obele, M. C.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Umennabuife, U. M.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Onukwuli, O. D.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of coatings technology and research</subfield><subfield code="d">Blue Bell, Pa., 2004</subfield><subfield code="g">16(2019), 6 vom: 21. 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Synthesis of rubber seed oil waterborne alkyd resin from glucitol

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