Lignin-Based Bio-Oil Mimic as Biobased Resin for Composite Applications
Lignin is an abundant renewable raw material that has the potential to yield valuable bio-oils consisting of aromatic chemicals when strategically depolymerized. In order to determine if lignin-based bio-oils can be utilized in the development of biobased vinyl ester resins without the need of exten...
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Veröffentlicht in: | ACS sustainable chemistry & engineering 2013-04, Vol.1 (4), p.419-426 |
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description | Lignin is an abundant renewable raw material that has the potential to yield valuable bio-oils consisting of aromatic chemicals when strategically depolymerized. In order to determine if lignin-based bio-oils can be utilized in the development of biobased vinyl ester resins without the need of extensive and costly separations, a methacrylated lignin-based bio-oil mimic (MBO) was generated and utilized as a low viscosity vinyl ester resin (30.3 cP at 25 °C) and as a reactive diluent in a standard commercial vinyl ester resin. MBO was comprised of phenol, guaiacols, and catechols that were methacrylated by esterification with methacrylic anhydride and a catalytic amount of 4-dimethylaminopyridine. Curing the resin produced hard transparent thermosets that possessed near complete conversion of free radical polymerizable groups as per near-infrared spectroscopy. Temperatures of maximum decomposition rate (≥400 °C) and initial decomposition temperatures (≥300 °C) were measured by means of thermo-gravimetric analysis (TGA). Glass transition temperatures ≥115 °C and storage moduli ≥2.5 GPa at 25 °C were measured by dynamic mechanical analysis (DMA). Overall, high-performance lignin-based thermosets were synthesized possessing comparable thermo-gravimetric and thermo-mechanical properties to commercial petroleum- and vinyl ester-based thermosets. |
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In order to determine if lignin-based bio-oils can be utilized in the development of biobased vinyl ester resins without the need of extensive and costly separations, a methacrylated lignin-based bio-oil mimic (MBO) was generated and utilized as a low viscosity vinyl ester resin (30.3 cP at 25 °C) and as a reactive diluent in a standard commercial vinyl ester resin. MBO was comprised of phenol, guaiacols, and catechols that were methacrylated by esterification with methacrylic anhydride and a catalytic amount of 4-dimethylaminopyridine. Curing the resin produced hard transparent thermosets that possessed near complete conversion of free radical polymerizable groups as per near-infrared spectroscopy. Temperatures of maximum decomposition rate (≥400 °C) and initial decomposition temperatures (≥300 °C) were measured by means of thermo-gravimetric analysis (TGA). Glass transition temperatures ≥115 °C and storage moduli ≥2.5 GPa at 25 °C were measured by dynamic mechanical analysis (DMA). 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Temperatures of maximum decomposition rate (≥400 °C) and initial decomposition temperatures (≥300 °C) were measured by means of thermo-gravimetric analysis (TGA). Glass transition temperatures ≥115 °C and storage moduli ≥2.5 GPa at 25 °C were measured by dynamic mechanical analysis (DMA). 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Eng</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>1</volume><issue>4</issue><spage>419</spage><epage>426</epage><pages>419-426</pages><issn>2168-0485</issn><eissn>2168-0485</eissn><abstract>Lignin is an abundant renewable raw material that has the potential to yield valuable bio-oils consisting of aromatic chemicals when strategically depolymerized. In order to determine if lignin-based bio-oils can be utilized in the development of biobased vinyl ester resins without the need of extensive and costly separations, a methacrylated lignin-based bio-oil mimic (MBO) was generated and utilized as a low viscosity vinyl ester resin (30.3 cP at 25 °C) and as a reactive diluent in a standard commercial vinyl ester resin. MBO was comprised of phenol, guaiacols, and catechols that were methacrylated by esterification with methacrylic anhydride and a catalytic amount of 4-dimethylaminopyridine. Curing the resin produced hard transparent thermosets that possessed near complete conversion of free radical polymerizable groups as per near-infrared spectroscopy. Temperatures of maximum decomposition rate (≥400 °C) and initial decomposition temperatures (≥300 °C) were measured by means of thermo-gravimetric analysis (TGA). Glass transition temperatures ≥115 °C and storage moduli ≥2.5 GPa at 25 °C were measured by dynamic mechanical analysis (DMA). Overall, high-performance lignin-based thermosets were synthesized possessing comparable thermo-gravimetric and thermo-mechanical properties to commercial petroleum- and vinyl ester-based thermosets.</abstract><pub>American Chemical Society</pub><doi>10.1021/sc3001492</doi><tpages>8</tpages></addata></record> |
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