메뉴 건너뛰기




Volumn 1, Issue 3, 2013, Pages 167-186

Biological oils as precursors to novel polymeric materials

Author keywords

Biological oils; Polymeric materials; Precursors

Indexed keywords

PETROLEUM INDUSTRY;

EID: 84903585764     PISSN: 21646325     EISSN: 21646341     Source Type: Journal    
DOI: 10.7569/JRM.2013.634112     Document Type: Article
Times cited : (21)

References (366)
  • 5
    • 78049376656 scopus 로고    scopus 로고
    • Vegetable oil-based polymeric materials: Synthesis, properties, and applications
    • Y. Xia and R.C. Larock, Vegetable oil-based polymeric materials: Synthesis, properties, and applications. Green Chem. 12, 1893-1909 (2010).
    • (2010) Green Chem. , vol.12 , pp. 1893-1909
    • Xia, Y.1    Larock, R.C.2
  • 9
    • 84953286797 scopus 로고    scopus 로고
    • Fluid catalytic cracking of vegetable oil: Effective strategies for enhanced gasoline production
    • Presented at the Detroit (unpublished).
    • M. Makkee, T.V.M. Rao, and M.M. Clavero, Fluid catalytic cracking of vegetable oil: Effective strategies for enhanced gasoline production. Presented at the 22nd North American Catalysis Society Meeting, Detroit, (2011) (unpublished).
    • (2011) 22nd North American Catalysis Society Meeting
    • Makkee, M.1    Rao, T.V.M.2    Clavero, M.M.3
  • 10
    • 77956425200 scopus 로고    scopus 로고
    • Effective gasoline production strategies by catalytic cracking of rapeseed vegetable oil in refinery conditions
    • T.V.M. Rao, M.M. Clavero, and M. Makkee, Effective gasoline production strategies by catalytic cracking of rapeseed vegetable oil in refinery conditions. ChemSus-Chem 3(7), 807-810 (2010).
    • (2010) ChemSus-Chem , vol.3 , Issue.7 , pp. 807-810
    • Rao, T.V.M.1    Clavero, M.M.2    Makkee, M.3
  • 11
    • 79953663072 scopus 로고    scopus 로고
    • Catalytic cracking of edible and non-edible oils for the production of biofuels
    • N. Taufiqurrahmi and S. Bhatia, Catalytic cracking of edible and non-edible oils for the production of biofuels. Energy Environ. Sci. 4, 1087-1112 (2011).
    • (2011) Energy Environ. Sci. , vol.4 , pp. 1087-1112
    • Taufiqurrahmi, N.1    Bhatia, S.2
  • 15
    • 38949184208 scopus 로고    scopus 로고
    • Polyurethanes from vegetable oils
    • Z.S. Petrovic, Polyurethanes from vegetable oils. Polym. Rev. 48(1), 109-155 (2008).
    • (2008) Polym. Rev. , vol.48 , Issue.1 , pp. 109-155
    • Petrovic, Z.S.1
  • 17
    • 34547423757 scopus 로고    scopus 로고
    • Network structure and properties of polyurethanes from soybean oil
    • Z.S. Petrovic, L. Yang, A. Zlatanic, W. Zhang, and I. Javni, Network structure and properties of polyurethanes from soybean oil. J. Appl. Polym. Sci. 105(5), 2717-2727 (2007).
    • (2007) J. Appl. Polym. Sci. , vol.105 , Issue.5 , pp. 2717-2727
    • Petrovic, Z.S.1    Yang, L.2    Zlatanic, A.3    Zhang, W.4    Javni, I.5
  • 18
    • 38649101887 scopus 로고    scopus 로고
    • Polyurethane networks from polyols obtained by hydroformylation of soybean oil
    • Z.S. Petrovic, A. Guo, I. Javni, I. Cvetkovic, and D.P. Hong, Polyurethane networks from polyols obtained by hydroformylation of soybean oil. Polym. Int. 57(2), 275-281 (2008).
    • (2008) Polym. Int. , vol.57 , Issue.2 , pp. 275-281
    • Petrovic, Z.S.1    Guo, A.2    Javni, I.3    Cvetkovic, I.4    Hong, D.P.5
  • 19
    • 0036737289 scopus 로고    scopus 로고
    • Structure and properties of triolein-based polyurethane networks
    • A. Zlatanic, Z.S. Petrovic, and K. Dusek, Structure and properties of triolein-based polyurethane networks. BioMacromolecules 3(5), 1048-1056 (2002).
    • (2002) BioMacromolecules , vol.3 , Issue.5 , pp. 1048-1056
    • Zlatanic, A.1    Petrovic, Z.S.2    Dusek, K.3
  • 20
    • 84866464910 scopus 로고    scopus 로고
    • Polyols and rigid polyurethane foams from cashew nut shell liquid
    • M. Ionescu, X. Wan, N. Bilic, and Z.S. Petrovic, Polyols and rigid polyurethane foams from cashew nut shell liquid. J. Polym. Environ. 20(3), 647-658 (2012).
    • (2012) J. Polym. Environ. , vol.20 , Issue.3 , pp. 647-658
    • Ionescu, M.1    Wan, X.2    Bilic, N.3    Petrovic, Z.S.4
  • 22
    • 0034325698 scopus 로고    scopus 로고
    • Structure and properties of halogenated and non-halogenated soybased polyols
    • A. Guo, Y.-J. Cho, and Z.S. Petrovic, Structure and properties of halogenated and non-halogenated soybased polyols. J. Polym.Sci. Part A Polym. Chem. 38, 3900-3910 (2000).
    • (2000) J. Polym.Sci. Part A Polym. Chem. , vol.38 , pp. 3900-3910
    • Guo, A.1    Cho, Y.-J.2    Petrovic, Z.S.3
  • 23
    • 84858116030 scopus 로고    scopus 로고
    • Polyurethanes from renewable resources
    • D.A. Babb, Polyurethanes from renewable resources. Adv. Polym. Sci. 245, 315-360 (2012).
    • (2012) Adv. Polym. Sci. , vol.245 , pp. 315-360
    • Babb, D.A.1
  • 24
    • 0027559449 scopus 로고
    • Factice from oil mixtures
    • S.M. Erhan and R. Kleiman, Factice from oil mixtures. J. Am. Oil Chem. Soc. 3(70), 309-311 (1993).
    • (1993) J. Am. Oil Chem. Soc. , vol.3 , Issue.70 , pp. 309-311
    • Erhan, S.M.1    Kleiman, R.2
  • 25
    • 84856262474 scopus 로고    scopus 로고
    • RAPRA Technology Ltd., Shabury, Shrewsbury, Shropshire, UK
    • R.B. Simpson, (Ed.), Rubber Basics, RAPRA Technology Ltd., Shabury, Shrewsbury, Shropshire, UK (2002).
    • (2002) Rubber Basics
    • Simpson, R.B.1
  • 26
    • 0028539280 scopus 로고
    • Polymerization of vegetable oils and their uses in printing inks
    • S.Z. Erhan and M.O. Bugby, Polymerization of vegetable oils and their uses in printing inks. J. Am. Oil Chem. Soc. 71(11), 1223-1226 (1994).
    • (1994) J. Am. Oil Chem. Soc. , vol.71 , Issue.11 , pp. 1223-1226
    • Erhan, S.Z.1    Bugby, M.O.2
  • 27
    • 84861678872 scopus 로고    scopus 로고
    • US Patent 5,713,990, assigned to The United States of America as represented by the Secretary of Agriculture ( February 3
    • S.Z. Erhan and M.O. Bagby, Vegetable Oil-based offset printing inks, US Patent 5,713,990, assigned to The United States of America as represented by the Secretary of Agriculture (February 3, 1998).
    • (1998) Vegetable Oil-Based Offset Printing Inks
    • Erhan, S.Z.1    Bagby, M.O.2
  • 28
    • 0033337905 scopus 로고    scopus 로고
    • Studies of thermal polymerization of vegetale oil with a differential scanning calorimeter
    • C. Wang and S. Erhan, Studies of thermal polymerization of vegetale oil with a differential scanning calorimeter. J. Am. Oil Chem. Soc. 76(10), 1211-1216 (1999).
    • (1999) J. Am. Oil Chem. Soc. , vol.76 , Issue.10 , pp. 1211-1216
    • Wang, C.1    Erhan, S.2
  • 29
    • 43149100369 scopus 로고
    • Heat polymerization of nonconjugated vegetable oils
    • I.M. Bernstein, Heat polymerization of nonconjugated vegetable oils. J. Polym. Sci. 3(6), 495-528 (1946).
    • (1946) J. Polym. Sci. , vol.3 , Issue.6 , pp. 495-528
    • Bernstein, I.M.1
  • 30
    • 84864891614 scopus 로고
    • Inter-and intramolecular polymerization in heat bodied linseed oil
    • R.F. Paschke and D.H. Wheeler, Inter-and intramolecular polymerization in heat bodied linseed oil. J. Am. Oil Chem. Soc. 31(5), 2008-2211 (1954).
    • (1954) J. Am. Oil Chem. Soc. , vol.31 , Issue.5 , pp. 2008-2211
    • Paschke, R.F.1    Wheeler, D.H.2
  • 31
    • 84953317590 scopus 로고
    • Thermal polymerisation of esters of drying oil acids
    • T.F. Bradley and R.W. Tess, Thermal polymerisation of esters of drying oil acids. Ind. Eng. Chem. 41(2), 310-319 (1949).
    • (1949) Ind. Eng. Chem. , vol.41 , Issue.2 , pp. 310-319
    • Bradley, T.F.1    Tess, R.W.2
  • 33
    • 5944241653 scopus 로고
    • Mechanism of the heat bodying linseed oil
    • P.O. Powers, Mechanism of the heat bodying linseed oil. J. Polym. Sci. 5(6), 741-743 (1950).
    • (1950) J. Polym. Sci. , vol.5 , Issue.6 , pp. 741-743
    • Powers, P.O.1
  • 34
    • 0012172620 scopus 로고
    • Heat bodying of drying oils
    • P.O. Powers, Heat bodying of drying oils. J. Am. Oil Chem. Soc. 27(11), 468-472 (1950).
    • (1950) J. Am. Oil Chem. Soc. , vol.27 , Issue.11 , pp. 468-472
    • Powers, P.O.1
  • 35
    • 84861712786 scopus 로고    scopus 로고
    • Evidence contrary to the accepted Diels-Alder mechanism in the thermal modification of vegetable oil
    • M. Arca, B.K. Sharma, N.P.J. Price, J.M. Perez, and K.M. Doll, Evidence contrary to the accepted Diels-Alder mechanism in the thermal modification of vegetable oil. J. Am. Oil Chem. Soc. 89(6), 987-994 (2012).
    • (2012) J. Am. Oil Chem. Soc. , vol.89 , Issue.6 , pp. 987-994
    • Arca, M.1    Sharma, B.K.2    Price, N.P.J.3    Perez, J.M.4    Doll, K.M.5
  • 38
    • 0028959042 scopus 로고
    • Mechanisms of free radical oxidation of unsaturated lipids
    • N.A. Porter, S.E. Caldwell, and K.A. Mills, Mechanisms of free radical oxidation of unsaturated lipids. Lipids 30(4), 277-290, (1995).
    • (1995) Lipids , vol.30 , Issue.4 , pp. 277-290
    • Porter, N.A.1    Caldwell, S.E.2    Mills, K.A.3
  • 39
  • 40
    • 0004196165 scopus 로고    scopus 로고
    • The Oily Press Ltd., Dundee, UK
    • E.N. Frankel, Lipid Oxidation, The Oily Press Ltd., Dundee, UK (1998).
    • (1998) Lipid Oxidation
    • Frankel, E.N.1
  • 42
    • 84925495331 scopus 로고
    • US Patent 2, 365,919, assigned to vested in the Alien Property Custodian (December 26
    • R. Uloth and M.-M. Cunradi, Agents suitable for improving lubricants, US Patent 2,365,919, assigned to vested in the Alien Property Custodian (December 26, 1944).
    • (1944) Agents Suitable for Improving Lubricants
    • Uloth, R.1    Cunradi, M.-M.2
  • 44
    • 33846429164 scopus 로고    scopus 로고
    • From oligomers to molecular giants of soybean oil in supercritical carbon dioxide medium
    • L. Zengshe, S. Brajendra, and S. Erhan, From oligomers to molecular giants of soybean oil in supercritical carbon dioxide medium. Biomacromolecules 8, 233-239 (2007).
    • (2007) Biomacromolecules , vol.8 , pp. 233-239
    • Zengshe, L.1    Brajendra, S.2    Erhan, S.3
  • 45
    • 0034299788 scopus 로고    scopus 로고
    • Thermosetting polymers from cationic copolymerization of tung oil: Synthesis and characterization
    • F. Li and R.C. Larock, Thermosetting polymers from cationic copolymerization of tung oil: Synthesis and characterization. J. Appl. Polym. Sci. 78(5), 1044-1056 (2000).
    • (2000) J. Appl. Polym. Sci. , vol.78 , Issue.5 , pp. 1044-1056
    • Li, F.1    Larock, R.C.2
  • 47
    • 0034325351 scopus 로고    scopus 로고
    • New soybean oil-styrene-divinylbenzene thermosetting copolymers. II: Dynamic mechanical properties
    • F. Li and R. Larock, New soybean oil-styrene-divinylbenzene thermosetting copolymers. II: Dynamic mechanical properties. J. Polym. Sci. Part B Polym. Phys. 38(11), 2721-2738 (2000).
    • (2000) J. Polym. Sci. Part B Polym. Phys. , vol.38 , Issue.11 , pp. 2721-2738
    • Li, F.1    Larock, R.2
  • 48
    • 0035946744 scopus 로고    scopus 로고
    • New soybean oil-styrene-divinylbenzene thermosetting copolymers. I: Synthesis and characterization
    • F. Li and R. Larock, New soybean oil-styrene-divinylbenzene thermosetting copolymers. I: Synthesis and characterization. J. Appl. Polym. Sci. 80(4), 658-670 (2001).
    • (2001) J. Appl. Polym. Sci. , vol.80 , Issue.4 , pp. 658-670
    • Li, F.1    Larock, R.2
  • 49
    • 0035151933 scopus 로고    scopus 로고
    • New soybean oil-styrene-divinylbenzene thermosetting copolymers. III: Tensile stressstrain behavior
    • F. Li and R. Larock, New soybean oil-styrene-divinylbenzene thermosetting copolymers. III: Tensile stressstrain behavior. J. Polym. Sci. Part B Polym. Phys. 39(1), 60-77 (2001).
    • (2001) J. Polym. Sci. Part B Polym. Phys. , vol.39 , Issue.1 , pp. 60-77
    • Li, F.1    Larock, R.2
  • 50
    • 0343941540 scopus 로고    scopus 로고
    • Fish oil thermosetting polymers: Creep and recovery behavior
    • F. Li, R. Larock, and J. Otaigbe, Fish oil thermosetting polymers: Creep and recovery behavior. Polymer 41(13), 4849-4862 (2000).
    • (2000) Polymer , vol.41 , Issue.13 , pp. 4849-4862
    • Li, F.1    Larock, R.2    Otaigbe, J.3
  • 51
    • 0343081371 scopus 로고    scopus 로고
    • Fish oil thermosetting polymer: Synthesis, structure, properties and their relationships
    • F. Li, D. Marks, R. Larock, and J. Otaigbe, Fish oil thermosetting polymer: Synthesis, structure, properties and their relationships. Polymer 41(22), 7925-7939 (2000).
    • (2000) Polymer , vol.41 , Issue.22 , pp. 7925-7939
    • Li, F.1    Marks, D.2    Larock, R.3    Otaigbe, J.4
  • 53
    • 0001356109 scopus 로고
    • Polymerization of drying oils. VI. Catalytic polymerization of fatty acids and esters with boron trifluoride and hydrogen fluoride
    • C.B. Croston, I.L. Tubb, J.C. Cowan, and H.M. Teeter, Polymerization of drying oils. VI. catalytic polymerization of fatty acids and esters with boron trifluoride and hydrogen fluoride. J. Am. Oil Chem. Soc. 29(8), 331-333 (1952).
    • (1952) J. Am. Oil Chem. Soc. , vol.29 , Issue.8 , pp. 331-333
    • Croston, C.B.1    Tubb, I.L.2    Cowan, J.C.3    Teeter, H.M.4
  • 54
    • 80052972024 scopus 로고
    • Contribution a I'étude de Ia polymerisation cationique de I'acide oléique et de ses dérivés. Etude des dimeres
    • S.M. Ghodssi, A.J. Petit, and H. Valot, Contribution a I'étude de Ia polymerisation cationique de I'acide oléique et de ses dérivés. Etude des dimeres. Bull. Soc. Chim. Fr. (4), 1461-1466 (1970).
    • (1970) Bull. Soc. Chim. Fr. , vol.4 , pp. 1461-1466
    • Ghodssi, S.M.1    Petit, A.J.2    Valot, H.3
  • 59
    • 70249085647 scopus 로고
    • UK Patent GB2, 172, 597, assigned to Union Camp (September 24
    • K.S. Hayes, Polymerization of fatty acids, UK Patent GB2,172,597, assigned to Union Camp (September 24, 1986).
    • (1986) Polymerization of Fatty Acids
    • Hayes, K.S.1
  • 63
    • 0000472249 scopus 로고
    • Epoxidation of oleic acid, methyl oleate and oleyl alcohol with perbenzoic acid
    • D. Swern, T.W. Findley, and J.T. Scanlan, Epoxidation of oleic acid, methyl oleate and oleyl alcohol with perbenzoic acid. J. Am. Chem. Soc. 66(11), 1925-1927 (1944).
    • (1944) J. Am. Chem. Soc. , vol.66 , Issue.11 , pp. 1925-1927
    • Swern, D.1    Findley, T.W.2    Scanlan, J.T.3
  • 64
    • 0001540220 scopus 로고
    • Hydroxylation of monounsaturated fatty materials with hydrogen peroxide
    • D. Swern, G.N. Billen, T.W. Findley, and J.T. Scanlan, Hydroxylation of monounsaturated fatty materials with hydrogen peroxide. J. Am. Chem. Soc. 67, 1786-1789 (1945).
    • (1945) J. Am. Chem. Soc. , vol.67 , pp. 1786-1789
    • Swern, D.1    Billen, G.N.2    Findley, T.W.3    Scanlan, J.T.4
  • 67
    • 84953251974 scopus 로고
    • US Patent 3, 328, 430, assigned to Archers-Daniels-Middland Co. ( June 27
    • L.I. Hansen and A.G. Coutsicos, Epoxidation Process, US Patent 3,328,430, assigned to Archers-Daniels-Middland Co. (June 27, 1967).
    • (1967) Epoxidation Process
    • Hansen, L.I.1    Coutsicos, A.G.2
  • 69
    • 0002995157 scopus 로고
    • Epoxidation of fish oil, kinetic and optimization model
    • J. Wisniak and E. Navarrete, Epoxidation of fish oil, kinetic and optimization model. Ind. Eng. Chem. Prod. Res. Develop. 9(1), 33-41 (1970).
    • (1970) Ind. Eng. Chem. Prod. Res. Develop. , vol.9 , Issue.1 , pp. 33-41
    • Wisniak, J.1    Navarrete, E.2
  • 70
    • 0030128030 scopus 로고    scopus 로고
    • Epoxidation of natural triglycerides with ethylmethyldioxirane
    • P.E. Sonnet and T.A. Foglia, Epoxidation of natural triglycerides with ethylmethyldioxirane. J. Am. Oil Chem. Soc. 73(4), 461-464 (1996).
    • (1996) J. Am. Oil Chem. Soc. , vol.73 , Issue.4 , pp. 461-464
    • Sonnet, P.E.1    Foglia, T.A.2
  • 71
    • 34447129755 scopus 로고    scopus 로고
    • Chemical routes for the transformation of biomass into chemicals
    • A. Corma, S. Iborra, and A. Velty, Chemical routes for the transformation of biomass into chemicals. Chem. Rev. 107, 2411-2502 (2007).
    • (2007) Chem. Rev. , vol.107 , pp. 2411-2502
    • Corma, A.1    Iborra, S.2    Velty, A.3
  • 72
    • 0011797363 scopus 로고
    • Epoxidation of fatty acid esters with aqueous hydrogen peroxide in the presence of molybdenum oxide-tributyltin chloride on charcoal catalyst
    • Y. Itoi, M. Inoue, and S. Enomoto, Epoxidation of fatty acid esters with aqueous hydrogen peroxide in the presence of molybdenum oxide-tributyltin chloride on charcoal catalyst. Bull. Chem. Soc. Jpn. 59(12), 3941-3943 (1986).
    • (1986) Bull. Chem. Soc. Jpn. , vol.59 , Issue.12 , pp. 3941-3943
    • Itoi, Y.1    Inoue, M.2    Enomoto, S.3
  • 73
    • 0040539401 scopus 로고
    • Epoxidation of fatty acid methyl esters with organic hydroperoxides and molybdenum oxide
    • A. Debal, G. Rafaralahitsimba, and E. Ucciani, Epoxidation of fatty acid methyl esters with organic hydroperoxides and molybdenum oxide. Fett Wiss Technol. -Fat Sci.Technol. 95(6), 236-239 (1993).
    • (1993) Fett Wiss Technol. Fat Sci.Technol. , vol.95 , Issue.6 , pp. 236-239
    • Debal, A.1    Rafaralahitsimba, G.2    Ucciani, E.3
  • 74
    • 33751392088 scopus 로고
    • Epoxidized triglycerides as renewable monomers in photoinitiated cationic polymerization
    • J.V. Crivello and R. Narayan, Epoxidized triglycerides as renewable monomers in photoinitiated cationic polymerization. Chem. Mater. 4(3), 692-699 (1992).
    • (1992) Chem. Mater. , vol.4 , Issue.3 , pp. 692-699
    • Crivello, J.V.1    Narayan, R.2
  • 75
    • 84984138902 scopus 로고
    • Kinetics and mechanism of the epoxidation of unsaturated fatty acids
    • M.E. Abraham and R.F. Benenati, Kinetics and mechanism of the epoxidation of unsaturated fatty acids. AIChE J. 18(4), 807-811 (1972).
    • (1972) AIChE J. , vol.18 , Issue.4 , pp. 807-811
    • Abraham, M.E.1    Benenati, R.F.2
  • 76
    • 0021419845 scopus 로고
    • Chemical epoxidation of a natural unsaturated epoxy seed oil from vernoniagalamensis and a look at epoxy oil markets
    • K.D. Carlson and S.P. Chang, Chemical epoxidation of a natural unsaturated epoxy seed oil from vernoniagalamensis and a look at epoxy oil markets. J. Am. Oil Chem. Soc. 62(5), 934-939 (1985).
    • (1985) J. Am. Oil Chem. Soc. , vol.62 , Issue.5 , pp. 934-939
    • Carlson, K.D.1    Chang, S.P.2
  • 77
    • 0036474324 scopus 로고    scopus 로고
    • Epoxidation of soybean oil by the methyltrioxorhenium-CH2Cl2/H2O2 catalytic biphasic system
    • A.E. Gerbase, J.R. Gregório, M. Martinelli, M.C. Brasil, and A.N.F. Mendes, Epoxidation of soybean oil by the methyltrioxorhenium-CH2Cl2/H2O2 catalytic biphasic system. J. Am. Oil Chem. Soc. 79(2), 179-181 (2002).
    • (2002) J. Am. Oil Chem. Soc. , vol.79 , Issue.2 , pp. 179-181
    • Gerbase, A.E.1    Gregório, J.R.2    Martinelli, M.3    Brasil, M.C.4    Mendes, A.N.F.5
  • 78
    • 0036015288 scopus 로고    scopus 로고
    • Epoxidation of soybean oil in toluene with peroxoacetic and peroxoformic acids -Kinetics and side reactions
    • Z.S. Petrovic, A. Zlatanic, C. Lava, and S. Sinadinovic-Fisher, Epoxidation of soybean oil in toluene with peroxoacetic and peroxoformic acids -Kinetics and side reactions. Eur. J. Lipid Sci. Technol. 104, 293-299 (2002).
    • (2002) Eur. J. Lipid Sci. Technol. , vol.104 , pp. 293-299
    • Petrovic, Z.S.1    Zlatanic, A.2    Lava, C.3    Sinadinovic-Fisher, S.4
  • 79
    • 0042581241 scopus 로고
    • Castor oil epoxidation with isopropylbenzene hydroperoxide. Process optimization. Influence of variables. Kinetic study
    • P.J. Martinez de la Cuesta, E. Rus Martinez, and J.A. Garcia, Castor oil epoxidation with isopropylbenzene hydroperoxide. Process optimization. Influence of variables. Kinetic study. Grasas Y Aceites (Sevilla) 39(2), 82-88 (1988).
    • (1988) Grasas Y Aceites (Sevilla) , vol.39 , Issue.2 , pp. 82-88
    • Martinez De La Cuesta, P.J.1    Rus Martinez, E.2    Garcia, J.A.3
  • 80
    • 84953299485 scopus 로고
    • Epoxidation of corn oil with molecular-oxygen -influence of variables -kinetic study
    • P.J. Martinez de la Cuesta, E. Rus Martinez, and V. Roman Cortes, Epoxidation of corn oil with molecular-oxygen -influence of variables -kinetic study. Anales De Quimica 88(2), 197-204 (1992).
    • (1992) Anales De Quimica , vol.88 , Issue.2 , pp. 197-204
    • Martinez De La Cuesta, P.J.1    Rus Martinez, E.2    Roman Cortes, V.3
  • 81
    • 0003325497 scopus 로고
    • The kinetics of the acid-catalyzed formation of peracetic acid from acetic acid and hydrogen peroxide
    • Y. Sawaki and Y. Ogata, The kinetics of the acid-catalyzed formation of peracetic acid from acetic acid and hydrogen peroxide. Bull. Chem. Soc. Jpn. 38, 2103 (1965).
    • (1965) Bull. Chem. Soc. Jpn. , vol.38 , pp. 2103
    • Sawaki, Y.1    Ogata, Y.2
  • 84
    • 0028377930 scopus 로고
    • Epoxidation of lesquerella and limnanthes (meadowfoam) oils
    • K.D. Carlson, R. Kleiman, and M.O. Bagby, Epoxidation of lesquerella and limnanthes (meadowfoam) oils. J. Am. Oil Chem. Soc. 71(2), 175-182 (1994).
    • (1994) J. Am. Oil Chem. Soc. , vol.71 , Issue.2 , pp. 175-182
    • Carlson, K.D.1    Kleiman, R.2    Bagby, M.O.3
  • 85
    • 1842665366 scopus 로고
    • Epoxidation of monoenic fatty esters with cumylhydroperoxide and hexacarbonylmolybdenum
    • E. Ucciani, A. Bonfand, G. Rafaralahitsimba, and G. Cecchi, Epoxidation of monoenic fatty esters with cumylhydroperoxide and hexacarbonylmolybdenum. Rev. Fr. Corps Gras 39(9-10), 279-283 (1992).
    • (1992) Rev. Fr. Corps Gras , vol.39 , Issue.9-10 , pp. 279-283
    • Ucciani, E.1    Bonfand, A.2    Rafaralahitsimba, G.3    Cecchi, G.4
  • 86
    • 0040539401 scopus 로고
    • Epoxidation of fatty acid methyl esters with organic hydroperoxides and molybdenum oxide
    • E. Ucciani, A. Debal, and G. Rafaralahitsimba, Epoxidation of fatty acid methyl esters with organic hydroperoxides and molybdenum oxide. Eur. J. Lipid Sci. Technol 95(6), 236-239 (1993).
    • (1993) Eur. J. Lipid Sci. Technol , vol.95 , Issue.6 , pp. 236-239
    • Ucciani, E.1    Debal, A.2    Rafaralahitsimba, G.3
  • 88
    • 51249166454 scopus 로고
    • Kinetic studies of epoxidation and oxirane cleavage of palm olein methyl esters
    • L.H. Gan, S.H. Goh, and K.S. Ooi, Kinetic studies of epoxidation and oxirane cleavage of palm olein methyl esters. J. Am. Oil Chem. Soc. 69(4), 347-351 (1992).
    • (1992) J. Am. Oil Chem. Soc. , vol.69 , Issue.4 , pp. 347-351
    • Gan, L.H.1    Goh, S.H.2    Ooi, K.S.3
  • 89
    • 0035386931 scopus 로고    scopus 로고
    • Kinetics of "in situ" epoxidation of soybean oil in bulk catalyzed by ion exchange resin
    • S. Sinadinovic-Fišer, M. Jankovic, and Z.S. Petrovic, Kinetics of "in situ" epoxidation of soybean oil in bulk catalyzed by ion exchange resin. J. Am. Oil Chem. Soc. 78, 725 (2001).
    • (2001) J. Am. Oil Chem. Soc. , vol.78 , pp. 725
    • Sinadinovic-Fišer, S.1    Jankovic, M.2    Petrovic, Z.S.3
  • 91
    • 0004571336 scopus 로고
    • Insitu epoxidation of linseed oil in presence of ionexchange resins
    • B.M. Badran, F.M. Elmehelmy, and N.A. Ghanem, Insitu epoxidation of linseed oil in presence of ionexchange resins. J. Oil Colour Chem. Assoc. 59(8), 291-294 (1976).
    • (1976) J. Oil Colour Chem. Assoc. , vol.59 , Issue.8 , pp. 291-294
    • Badran, B.M.1    Elmehelmy, F.M.2    Ghanem, N.A.3
  • 93
    • 34250117245 scopus 로고
    • Mechanism of cationic polymerization of glycidic esters
    • Y.P. Getmanchuk and E.V. Blazhko, Mechanism of cationic polymerization of glycidic esters. Theor. Exp. Chem. 21(6), 686-690 (1985).
    • (1985) Theor. Exp. Chem. , vol.21 , Issue.6 , pp. 686-690
    • Getmanchuk, Y.P.1    Blazhko, E.V.2
  • 94
    • 84755160897 scopus 로고    scopus 로고
    • Ring-opening polymerization of epoxidized soybean oil
    • Z. Liu and S.Z. Erhan, Ring-opening polymerization of epoxidized soybean oil. J. Am. Oil Chem. Soc. 87, 437-444 (2010).
    • (2010) J. Am. Oil Chem. Soc. , vol.87 , pp. 437-444
    • Liu, Z.1    Erhan, S.Z.2
  • 95
    • 0344901242 scopus 로고
    • Reaction scheme in the cationic polymerization of substituted epoxides
    • Y. Kawakami, A. Ogawa, and Y. Yamashita, Reaction scheme in the cationic polymerization of substituted epoxides. J. Polym. Sci. Polym. Chem. Ed. 17, 3785-3792 (1979).
    • (1979) J. Polym. Sci. Polym. Chem. Ed. , vol.17 , pp. 3785-3792
    • Kawakami, Y.1    Ogawa, A.2    Yamashita, Y.3
  • 96
    • 30344472689 scopus 로고    scopus 로고
    • Synthesis and characterization of polyurethanes from epoxidized methyl oleate based polyether polyols as renewable resources
    • G. Lligadas, J.C. Ronda, M. Galia, U. Biermann, and J.O. Metzger, Synthesis and characterization of polyurethanes from epoxidized methyl oleate based polyether polyols as renewable resources. J. Polym. Sci. Part A Polym. Chem. 44, 634-645 (2006).
    • (2006) J. Polym. Sci. Part A Polym. Chem. , vol.44 , pp. 634-645
    • Lligadas, G.1    Ronda, J.C.2    Galia, M.3    Biermann, U.4    Metzger, J.O.5
  • 97
    • 0000913383 scopus 로고
    • Polymers from renewable resources: Polyester resins and blends based upon anhydride-cured epoxidized soybean oil
    • J. Roesch and R. Muelhaupt, Polymers from renewable resources: Polyester resins and blends based upon anhydride-cured epoxidized soybean oil. Polym. Bull. (Berlin) 31(6), 679-685 (1993).
    • (1993) Polym. Bull. (Berlin) , vol.31 , Issue.6 , pp. 679-685
    • Roesch, J.1    Muelhaupt, R.2
  • 98
    • 84953304903 scopus 로고    scopus 로고
    • Epoxy resins from vegetable oils
    • SPE, San Francisco
    • Z.S. Petrovic, W. Zhang, R. Miller, and I. Javni, Epoxy Resins from Vegetable Oils, in ANTEC, pp. 1-3, SPE, San Francisco (2002).
    • (2002) ANTEC , pp. 1-3
    • Petrovic, Z.S.1    Zhang, W.2    Miller, R.3    Javni, I.4
  • 100
    • 0033102171 scopus 로고    scopus 로고
    • The cationic ring-opening polymerization of 7-tetradecene oxide with methyl trifluoromethansulfonate. An investigation of the mechanism and the kinetics by means of 1H, 13C and 19F NMR
    • M. Clericuzio, S. Cobianco, M. Fabbi, A. Lezzi, and L. Montanari, The cationic ring-opening polymerization of 7-tetradecene oxide with methyl trifluoromethansulfonate. An investigation of the mechanism and the kinetics by means of 1H, 13C and 19F NMR. Polymer 40, 1839-1851 (1999).
    • (1999) Polymer , vol.40 , pp. 1839-1851
    • Clericuzio, M.1    Cobianco, S.2    Fabbi, M.3    Lezzi, A.4    Montanari, L.5
  • 101
    • 0031164864 scopus 로고    scopus 로고
    • Fabrication and mechanical characterization of glass fiber reinforced UV-cured composites from epoxidized vegetable oils
    • J.V. Crivello, R. Narayan, and S.S. Sternstein, Fabrication and mechanical characterization of glass fiber reinforced UV-cured composites from epoxidized vegetable oils. J. Appl. Polym. Sci. 64, 2073-2087 (1997).
    • (1997) J. Appl. Polym. Sci. , vol.64 , pp. 2073-2087
    • Crivello, J.V.1    Narayan, R.2    Sternstein, S.S.3
  • 104
    • 0006787420 scopus 로고    scopus 로고
    • The use of renewable resources -possibilities and limitations
    • R. Muelhaupt, The use of renewable resources -possibilities and limitations. Chimia 50(5), 191-198 (1996).
    • (1996) Chimia , vol.50 , Issue.5 , pp. 191-198
    • Muelhaupt, R.1
  • 105
    • 78650867798 scopus 로고    scopus 로고
    • Thermal and mechanical properties of anhydride-cured epoxy resins with different contents of biobased epoxidized soybean oil
    • F.I. Altuna, L.H. Espósito, R.A. Ruseckaite, and P.M. Stefani, Thermal and mechanical properties of anhydride-cured epoxy resins with different contents of biobased epoxidized soybean oil. J. Appl. Polym. Sci. 120(2), 789-798 (2011).
    • (2011) J. Appl. Polym. Sci. , vol.120 , Issue.2 , pp. 789-798
    • Altuna, F.I.1    Espósito, L.H.2    Ruseckaite, R.A.3    Stefani, P.M.4
  • 111
    • 72649103537 scopus 로고    scopus 로고
    • A novel vegetable oil-lactate hybrid monomer for synthesis of high-Tg polyurethanes
    • S. Miao, S. Zhang, Z. Su, and P. Wang, A novel vegetable oil-lactate hybrid monomer for synthesis of high-Tg polyurethanes. J. Polym. Sci Part A Polym. Chem. 48, 243-250 (2010).
    • (2010) J. Polym. Sci Part A Polym. Chem. , vol.48 , pp. 243-250
    • Miao, S.1    Zhang, S.2    Su, Z.3    Wang, P.4
  • 112
    • 51249164416 scopus 로고
    • Polyhydroxy fatty acids and their derivatives from plant oils
    • B. Dahlke, S. Hellbardt, M. Paetow, and W.H. Zech, Polyhydroxy fatty acids and their derivatives from plant oils. J. Am. Oil Chem. Soc. 72(3), 349-353 (1995).
    • (1995) J. Am. Oil Chem. Soc. , vol.72 , Issue.3 , pp. 349-353
    • Dahlke, B.1    Hellbardt, S.2    Paetow, M.3    Zech, W.H.4
  • 113
    • 0009710414 scopus 로고
    • Polyols on the basis of oleochemical raw materials
    • B. Gruber, R. Hoefer, H. Kluth, and A. Meffert, Polyols on the basis of oleochemical raw materials. Fett Wiss. Technol. 89(4), 147-151 (1987).
    • (1987) Fett Wiss. Technol. , vol.89 , Issue.4 , pp. 147-151
    • Gruber, B.1    Hoefer, R.2    Kluth, H.3    Meffert, A.4
  • 115
    • 78650396586 scopus 로고    scopus 로고
    • Catalyst-and solventfree "Click" chemistry: A facile approach to obtain cross-linked biopolymers from soybean oil
    • J. Hong, Q. Luo, and B.K. Shah, Catalyst-and solventfree "Click" chemistry: A facile approach to obtain cross-linked biopolymers from soybean oil. Biomacromolecules 11, 2960-2965 (2010).
    • (2010) Biomacromolecules , vol.11 , pp. 2960-2965
    • Hong, J.1    Luo, Q.2    Shah, B.K.3
  • 118
    • 0036199037 scopus 로고    scopus 로고
    • The effect of fatty acid composition on the acrylation kinetics of epoxidized triacylglycerols
    • J. La Scala and R.P. Wool, The effect of fatty acid composition on the acrylation kinetics of epoxidized triacylglycerols. J. Am. Oil Chem. Soc. 79(1), 59-63 (2002).
    • (2002) J. Am. Oil Chem. Soc. , vol.79 , Issue.1 , pp. 59-63
    • La Scala, J.1    Wool, R.P.2
  • 119
    • 34248338851 scopus 로고    scopus 로고
    • Vegetable oils in production of polymers and plastics
    • F. Shahidi, (Ed.)
    • S.S. Narine and X. Kong, Vegetable Oils in Production of Polymers and Plastics, in Bailey's Industrial Oil and Fat Products, F. Shahidi, (Ed.), pp. 279-306, Vol. 6, (2005).
    • (2005) Bailey's Industrial Oil and Fat Products , vol.6 , pp. 279-306
    • Narine, S.S.1    Kong, X.2
  • 121
    • 35548970309 scopus 로고    scopus 로고
    • New hybrid latexes from a soybean oil-based waterborne polyurethane and acrylics via emulsion polymerization
    • Y. Lu and R.C. Larock, New hybrid latexes from a soybean oil-based waterborne polyurethane and acrylics via emulsion polymerization. Biomacromolecules 8, 3108-3114 (2007).
    • (2007) Biomacromolecules , vol.8 , pp. 3108-3114
    • Lu, Y.1    Larock, R.C.2
  • 123
    • 80053028667 scopus 로고    scopus 로고
    • Thermosetting allyl resins derived from soybean oil
    • Q. Luo, M. Liu, Y.F. Xu, M. Ionescu, and Z.S. Petrovic, Thermosetting allyl resins derived from soybean oil. Macromolecules 44, 7149-7157 (2011).
    • (2011) Macromolecules , vol.44 , pp. 7149-7157
    • Luo, Q.1    Liu, M.2    Xu, Y.F.3    Ionescu, M.4    Petrovic, Z.S.5
  • 124
    • 84867480896 scopus 로고    scopus 로고
    • Thermosetting allyl resins derived from soybean fatty acids
    • Q. Luo, M. Liu, Y.F. Xu, M. Ionescu, and Z.S. Petrovic, Thermosetting allyl resins derived from soybean fatty acids. J. Appl. Polym. Sci. 127(1), 432-438 (2012).
    • (2012) J. Appl. Polym. Sci. , vol.127 , Issue.1 , pp. 432-438
    • Luo, Q.1    Liu, M.2    Xu, Y.F.3    Ionescu, M.4    Petrovic, Z.S.5
  • 126
    • 0031169683 scopus 로고    scopus 로고
    • Oleochemical polyols -A new raw material source for polyurethane coatings and floorings
    • R. Hoefer, P. Daute, R. Grutzmacher, and A. Westfechtel, Oleochemical polyols -A new raw material source for polyurethane coatings and floorings. J. Coat. Technol. 69(869), 65-72 (1997).
    • (1997) J. Coat. Technol. , vol.69 , Issue.869 , pp. 65-72
    • Hoefer, R.1    Daute, P.2    Grutzmacher, R.3    Westfechtel, A.4
  • 127
    • 84855913113 scopus 로고    scopus 로고
    • From vegetable oils to polyurethanes: Synthetic routes to polyols and main industrial products
    • M. Desroches, M. Escouvois, R. Auvergne, S. Caillol, and B. Boutevin, From vegetable oils to polyurethanes: Synthetic routes to polyols and main industrial products. Polym. Rev. 52(1), 38-79 (2012).
    • (2012) Polym. Rev. , vol.52 , Issue.1 , pp. 38-79
    • Desroches, M.1    Escouvois, M.2    Auvergne, R.3    Caillol, S.4    Boutevin, B.5
  • 128
    • 84867957605 scopus 로고    scopus 로고
    • Applied hydroformylation
    • R. Franke, D. Selent, and A. Bö rner, Applied hydroformylation. Chem. Rev. 112, 5675-5732 (2012).
    • (2012) Chem. Rev. , vol.112 , pp. 5675-5732
    • Franke, R.1    Selent, D.2    Börner, A.3
  • 132
    • 1942490415 scopus 로고    scopus 로고
    • Polyols and polyurethanes from hydroformylation of soybean oil
    • A. Guo, D. Demydov, W. Zhang, and Z.S. Petrovic, Polyols and polyurethanes from hydroformylation of soybean oil. J. Polym. Environ. 10(1/2), 49-52 (2002).
    • (2002) J. Polym. Environ. , vol.10 , Issue.1-2 , pp. 49-52
    • Guo, A.1    Demydov, D.2    Zhang, W.3    Petrovic, Z.S.4
  • 135
    • 51249189126 scopus 로고
    • Selective Hydroformylation of Polyunsaturated Fats with a Rh-PPh3 Catalyst
    • E.N. Frankel and F.L. Thomas, Selective Hydroformylation of Polyunsaturated Fats with a Rh-PPh3 Catalyst. J. Am. Oil Chem. Soc. 49, 10-14 (1972).
    • (1972) J. Am. Oil Chem. Soc. , vol.49 , pp. 10-14
    • Frankel, E.N.1    Thomas, F.L.2
  • 136
    • 0036922743 scopus 로고    scopus 로고
    • The kinetics of the hydroformylation of soybean oil by ligand modified homogeneous rhodium catalysis
    • P. Kandanarachchi, A. Guo, D. Demydov, and Z. Petrovic, The kinetics of the hydroformylation of soybean oil by ligand modified homogeneous rhodium catalysis. J. Oil Chem.Soc. 79, 1221-1225 (2002).
    • (2002) J. Oil Chem.Soc. , vol.79 , pp. 1221-1225
    • Kandanarachchi, P.1    Guo, A.2    Demydov, D.3    Petrovic, Z.4
  • 138
    • 0007186020 scopus 로고
    • Rigid urethane foams from hydroxymethylated castor oil, safflower oil, oleic safflower oil, and polyol esters of castor acids
    • C.K. Lyon, V.H. Garrett, and E.N. Frankel, Rigid urethane foams from hydroxymethylated castor oil, safflower oil, oleic safflower oil, and polyol esters of castor acids. J. Am. Oil Chem. Soc. 51, 331-334 (1974).
    • (1974) J. Am. Oil Chem. Soc. , vol.51 , pp. 331-334
    • Lyon, C.K.1    Garrett, V.H.2    Frankel, E.N.3
  • 139
    • 0001591889 scopus 로고
    • Hydroformylation with recycled rhodium catalyst and one-step esterification-acetalation: A process for methyl 9(10)-methoxy-methylenestearate from oleic acid
    • R.A. Awl, E.N. Frankel, and E.H. Pryde, Hydroformylation with recycled rhodium catalyst and one-step esterification-acetalation: A process for methyl 9(10)-methoxy-methylenestearate from oleic acid. J. Am. Oil Chem. Soc. 53(5), 190-195 (1976).
    • (1976) J. Am. Oil Chem. Soc. , vol.53 , Issue.5 , pp. 190-195
    • Awl, R.A.1    Frankel, E.N.2    Pryde, E.H.3
  • 142
    • 78651422333 scopus 로고
    • Some esters of Mono-Di-and Tricarboxystearic acid as plasticizers: Preparation and evaluation
    • E.J. Dufek and E.N. Frankel, Some esters of Mono-, Di-, and Tricarboxystearic acid as plasticizers: Preparation and evaluation. J. Am. Oil Chem. Soc. 53(5), 198-203 (1976).
    • (1976) J. Am. Oil Chem. Soc. , vol.53 , Issue.5 , pp. 198-203
    • Dufek, E.J.1    Frankel, E.N.2
  • 143
    • 0000300799 scopus 로고
    • Methyl 9(10)-formylstearate by selective hydroformylation of oleic oil
    • E.N. Frankel, Methyl 9(10)-formylstearate by selective hydroformylation of oleic oil. J. Am. Oil Chem. Soc. 48, 248-253 (1971).
    • (1971) J. Am. Oil Chem. Soc. , vol.48 , pp. 248-253
    • Frankel, E.N.1
  • 144
    • 0015690689 scopus 로고
    • Selective hydroformylation of unsaturated fatty acid esters
    • E.N. Frankel, Selective hydroformylation of unsaturated fatty acid esters. Ann. NY Acad. Sci. 214, 79-93 (1973).
    • (1973) Ann. NY Acad. Sci. , vol.214 , pp. 79-93
    • Frankel, E.N.1
  • 146
    • 51249188614 scopus 로고
    • Catalytic hydroformylation of unsaturated fatty derivatives with cobalt carbonyl
    • E.N. Frankel, Catalytic hydroformylation of unsaturated fatty derivatives with cobalt carbonyl. J. Am. Oil Chem. Soc. 53(4), 138-141 (1976).
    • (1976) J. Am. Oil Chem. Soc. , vol.53 , Issue.4 , pp. 138-141
    • Frankel, E.N.1
  • 147
    • 0001372849 scopus 로고
    • Hydroformylation of methyl oleate with a recycled rhodium catalyst and estimated costs for a batch process
    • J.P. Friedrich, Hydroformylation of methyl oleate with a recycled rhodium catalyst and estimated costs for a batch process. J. Am. Oil Chem. Soc. 50(11), 455-458 (1973).
    • (1973) J. Am. Oil Chem. Soc. , vol.50 , Issue.11 , pp. 455-458
    • Friedrich, J.P.1
  • 148
    • 0018019296 scopus 로고
    • Low-pressure hydroformylation of methyl oleate with an activated rhodium catalyst
    • J.P. Friedrich, Low-pressure hydroformylation of methyl oleate with an activated rhodium catalyst. Ind. Eng. Chem. Prod. Res. Dev. 17(3), 205-207 (1978).
    • (1978) Ind. Eng. Chem. Prod. Res. Dev. , vol.17 , Issue.3 , pp. 205-207
    • Friedrich, J.P.1
  • 149
    • 0020709472 scopus 로고
    • Hydroformylation of unsaturated fatty acids
    • E.H. Pride, Hydroformylation of unsaturated fatty acids. J. Am. Oil Chem. Soc. 61(2), 419-425 (1984).
    • (1984) J. Am. Oil Chem. Soc. , vol.61 , Issue.2 , pp. 419-425
    • Pride, E.H.1
  • 150
    • 51249192514 scopus 로고
    • Reactions of carbon monoxide with unsaturated fatty acids and derivatives: A review
    • E.H. Pride, E.N. Frankel, and J.C. Cowan, Reactions of carbon monoxide with unsaturated fatty acids and derivatives: A review. J. Am. Oil Chem. Soc. 49, 451-456 (1972).
    • (1972) J. Am. Oil Chem. Soc. , vol.49 , pp. 451-456
    • Pride, E.H.1    Frankel, E.N.2    Cowan, J.C.3
  • 151
    • 33748857955 scopus 로고    scopus 로고
    • Structure-property relationships in polyurethanes derived from soybean oil
    • A. Guo, W. Zhang, and Z.S. Petrovic, Structure-property relationships in polyurethanes derived from soybean oil. J. Mater. Sci. 41(15), 4914-4920 (2006).
    • (2006) J. Mater. Sci. , vol.41 , Issue.15 , pp. 4914-4920
    • Guo, A.1    Zhang, W.2    Petrovic, Z.S.3
  • 152
    • 85058112902 scopus 로고    scopus 로고
    • Polyurethanes
    • H.R. Kriecheldorf, O. Nuyken, and G. Swift,(Eds.), Marcel Dekker, Inc., New York
    • Z.S. Petrovic, Polyurethanes, in Handbook of Polymer Synthesis, H.R. Kriecheldorf, O. Nuyken, and G. Swift,(Eds.), pp. 503-540. Marcel Dekker, Inc., New York (2005).
    • (2005) Handbook of Polymer Synthesis , pp. 503-540
    • Petrovic, Z.S.1
  • 156
    • 65249111543 scopus 로고    scopus 로고
    • Fatty acid-derived diisocyanate and biobased polyurethane produced from vegetable oil: Synthesis, polymerization, and characterization
    • L. Hojabri, X. Kong, and S.S. Narine, Fatty acid-derived diisocyanate and biobased polyurethane produced from vegetable oil: Synthesis, polymerization, and characterization. Biomacromolecules 10(4), 884-891 (2009).
    • (2009) Biomacromolecules , vol.10 , Issue.4 , pp. 884-891
    • Hojabri, L.1    Kong, X.2    Narine, S.S.3
  • 157
    • 49549091354 scopus 로고    scopus 로고
    • Biobased polyisocyanates from plant oil triglycerides: Synthesis, polymerization, and characterization
    • G. Çayli and S. Küsefoʇlu, Biobased polyisocyanates from plant oil triglycerides: Synthesis, polymerization, and characterization. J. Appl. Polym. Sci. 109(5), 2948-2955 (2008).
    • (2008) J. Appl. Polym. Sci. , vol.109 , Issue.5 , pp. 2948-2955
    • Çayli, G.1    Küsefoʇlu, S.2
  • 158
    • 75449118951 scopus 로고    scopus 로고
    • Isothiocyanate derivatives of soybean oil triglycerides: Synthesis, characterization, and polymerization with polyols and polyamines
    • G. Çayli and S. Küsefoʇlu, Isothiocyanate derivatives of soybean oil triglycerides: Synthesis, characterization, and polymerization with polyols and polyamines. J. Appl. Polym. Sci. 116(1), 125-131 (2010).
    • (2010) J. Appl. Polym. Sci. , vol.116 , Issue.1 , pp. 125-131
    • Çayli, G.1    Küsefoʇlu, S.2
  • 159
    • 84953220760 scopus 로고    scopus 로고
    • Advances in the use of BiOH® polyols in polyurethanes chapter 11
    • P.B. Smith and R.A. Gross, (Eds.), American Chemical Society
    • T.W. Abraham, Advances in the Use of BiOH® Polyols in Polyurethanes Chapter 11, in Biobased Monomers, Polymers, and Materials, P.B. Smith and R.A. Gross, (Eds.), pp. 165-181. American Chemical Society, (2012).
    • (2012) Biobased Monomers, Polymers, and Materials , pp. 165-181
    • Abraham, T.W.1
  • 161
    • 78650286150 scopus 로고    scopus 로고
    • Plant oils as platform chemicals for polyurethane synthesis: Current state-of-The-art
    • G. Lligadas, J.C. Ronda, M. Galià, and V. Cádiz, Plant oils as platform chemicals for polyurethane synthesis: Current state-of-The-art. Biomacromolecules 11, 2825-2835 (2010).
    • (2010) Biomacromolecules , vol.11 , pp. 2825-2835
    • Lligadas, G.1    Ronda, J.C.2    Galià, M.3    Cádiz, V.4
  • 163
    • 84905648384 scopus 로고    scopus 로고
    • Polyurethanes from hybrid vegetable oil/petrochemical polyester polyols
    • G.F. Payne and P.B. Smith, (Eds.), ACS symposium series, Washington, DC
    • M. Ionescu, Y. Ji, W.M. Shirley, and Z.S. Petrovic, Polyurethanes from Hybrid Vegetable Oil/Petrochemical Polyester Polyols, in Renewable and Sustainable Polymers, G.F. Payne and P.B. Smith, (Eds.), pp. 73-93, Vol. 1063, ACS symposium series, Washington, DC (2011).
    • (2011) Renewable and Sustainable Polymers , vol.1063 , pp. 73-93
    • Ionescu, M.1    Ji, Y.2    Shirley, W.M.3    Petrovic, Z.S.4
  • 164
    • 38349041910 scopus 로고    scopus 로고
    • Effect of hyperbranched vegetable oil polyols on properties of flexible polyurethane foams
    • Z.S. Petrovic, I. Javni, X. Jing, D.P. Hong, and A. Guo, Effect of hyperbranched vegetable oil polyols on properties of flexible polyurethane foams. Mat. Sci. Forum 555, 459-466 (2007).
    • (2007) Mat. Sci. Forum , vol.555 , pp. 459-466
    • Petrovic, Z.S.1    Javni, I.2    Jing, X.3    Hong, D.P.4    Guo, A.5
  • 167
    • 85027952503 scopus 로고    scopus 로고
    • Solution properties of bio-based hyperbranched polyols investigated by multiple detection size exclusion chromatography
    • J. Milic, I. Teraoka, and Z.S. Petrovic, Solution properties of bio-based hyperbranched polyols investigated by multiple detection size exclusion chromatography. J. Appl. Polym. Sci. 125(S2), E586-E594 (2012).
    • (2012) J. Appl. Polym. Sci. , vol.125 , pp. E586-E594
    • Milic, J.1    Teraoka, I.2    Petrovic, Z.S.3
  • 168
    • 51249183728 scopus 로고
    • Recovery of solubilized rhodium from hydroformylated vegetable-oils and their methyl-esters
    • E.J. Dufek and G.R. List, Recovery of solubilized rhodium from hydroformylated vegetable-oils and their methyl-esters. J. Am. Oil Chem. Soc. 54(7), 276-278 (1977).
    • (1977) J. Am. Oil Chem. Soc. , vol.54 , Issue.7 , pp. 276-278
    • Dufek, E.J.1    List, G.R.2
  • 169
    • 84902704778 scopus 로고
    • US Patent 3, 787, 459, assigned to United States of America as represented by the secretary of Agriculture January 22
    • E.N. Frankel, Selective hydroformylation of unsaturated fatty compounds, US Patent 3,787,459, assigned to United States of America as represented by the secretary of Agriculture (January 22, 1974).
    • (1974) Selective Hydroformylation of Unsaturated Fatty Compounds
    • Frankel, E.N.1
  • 170
    • 0002000875 scopus 로고
    • Hydroformylation of methyl linoleate and linolenate with rhodium-triphenylphosphine catalyst
    • E.N. Frankel, F.L. Thomas, and W.L. Rohwedder, Hydroformylation of methyl linoleate and linolenate with rhodium-triphenylphosphine catalyst. Ind. Eng. Chem. Prod. Res. Dev. 12 (1), 47-53 (1973).
    • (1973) Ind. Eng. Chem. Prod. Res. Dev. , vol.12 , Issue.1 , pp. 47-53
    • Frankel, E.N.1    Thomas, F.L.2    Rohwedder, W.L.3
  • 171
    • 0037124245 scopus 로고    scopus 로고
    • Hydroformulation of vegetable oils and model compounds by ligand modified rhodium catalysis
    • P. Kandanarachchi, A. Guo, and Z. Petrovic, Hydroformulation of vegetable oils and model compounds by ligand modified rhodium catalysis. J. Mol. Catal. A 184(1-2), 65-71 (2002).
    • (2002) J. Mol. Catal. A , vol.184 , Issue.1-2 , pp. 65-71
    • Kandanarachchi, P.1    Guo, A.2    Petrovic, Z.3
  • 173
    • 16444366465 scopus 로고
    • Reduction of methyl oleate ozonolysis products to aldehydes with activated Zn
    • R.A. Awl and E.H. Pryde., Reduction of methyl oleate ozonolysis products to aldehydes with activated Zn. J. Am. Oil Chem. Soc. 43, 35-37 (1966).
    • (1966) J. Am. Oil Chem. Soc. , vol.43 , pp. 35-37
    • Awl, R.A.1    Pryde, E.H.2
  • 174
    • 0345453393 scopus 로고
    • New raw materials for oleochemical reactions
    • H. Eierdanz and F. Hirsinger, New raw materials for oleochemical reactions. Fett Wissenschaft Technologie 92(12), 463-467 (1990).
    • (1990) Fett Wissenschaft Technologie , vol.92 , Issue.12 , pp. 463-467
    • Eierdanz, H.1    Hirsinger, F.2
  • 175
    • 77951881586 scopus 로고    scopus 로고
    • Preparation of 9-hydroxynonanoic acid methyl ester by ozonolysis of vegetable oils and its polycondensation
    • I. Cvetkovic, J. Milic, M. Ionescu, and Z.S. Petrovic, Preparation of 9-hydroxynonanoic acid methyl ester by ozonolysis of vegetable oils and its polycondensation. Hem. Ind. 62(6), 319-328 (2008).
    • (2008) Hem. Ind. , vol.62 , Issue.6 , pp. 319-328
    • Cvetkovic, I.1    Milic, J.2    Ionescu, M.3    Petrovic, Z.S.4
  • 176
    • 16444362670 scopus 로고    scopus 로고
    • Structure and properties of polyurethanes prepared from triglyceride polyols by ozonolysis
    • Z.S. Petrovic, W. Zhang, and I. Javni, Structure and properties of polyurethanes prepared from triglyceride polyols by ozonolysis. Biomacromolecules 6(2), 713-719 (2005).
    • (2005) Biomacromolecules , vol.6 , Issue.2 , pp. 713-719
    • Petrovic, Z.S.1    Zhang, W.2    Javni, I.3
  • 177
    • 38949108147 scopus 로고    scopus 로고
    • Value-added chemicals from catalytic ozonation of vegetable oils
    • D. Graiver and R. Narayan, Value-added chemicals from catalytic ozonation of vegetable oils. Lipid Tech. 17(2), 31 (2006).
    • (2006) Lipid Tech. , vol.17 , Issue.2 , pp. 31
    • Graiver, D.1    Narayan, R.2
  • 179
    • 77951927268 scopus 로고    scopus 로고
    • A chemical route to high molecular weight vegetable oil-based polyhydroxyalkanoate
    • Z.S. Petrovic, J. Milic, Y. Xu, and I. Cvetkovic, A chemical route to high molecular weight vegetable oil-based polyhydroxyalkanoate. Macromolecules 43(9), 4120-4125 (2010).
    • (2010) Macromolecules , vol.43 , Issue.9 , pp. 4120-4125
    • Petrovic, Z.S.1    Milic, J.2    Xu, Y.3    Cvetkovic, I.4
  • 180
    • 0009579224 scopus 로고
    • Saponification resistant polyols for polyurethane applications based on oleochemical raw materials
    • P. Daute, R. Gruetzmacher, R. Hoefer, and A. Westfechtel, Saponification resistant polyols for polyurethane applications based on oleochemical raw materials. Fett Wissenschaft Technologie 95(3), 91-94 (1993).
    • (1993) Fett Wissenschaft Technologie , vol.95 , Issue.3 , pp. 91-94
    • Daute, P.1    Gruetzmacher, R.2    Hoefer, R.3    Westfechtel, A.4
  • 181
    • 0001530997 scopus 로고
    • Oxidation of unsaturated fatty acids with ruthenium and osmium tetroxide
    • T.A. Foglia, P.A. Barr, A.J. Malloy, and M.J. Costazo, Oxidation of unsaturated fatty acids with ruthenium and osmium tetroxide. J. Am. Oil Chem. Soc. 54, 870A (1977).
    • (1977) J. Am. Oil Chem. Soc. , vol.54 , pp. 870A
    • Foglia, T.A.1    Barr, P.A.2    Malloy, A.J.3    Costazo, M.J.4
  • 182
    • 0016080987 scopus 로고
    • Osmium tetroxide and its applications
    • W.P. Griffith, Osmium tetroxide and its applications. Platinum Metals Rev. 18(3), 94-96 (1974).
    • (1974) Platinum Metals Rev. , vol.18 , Issue.3 , pp. 94-96
    • Griffith, W.P.1
  • 184
    • 0001149771 scopus 로고
    • Castor oil as a way to fastcured polyurethane ureas
    • P. Knaub and Y. Camberlin, Castor oil as a way to fastcured polyurethane ureas. Eur.Polym.J. 22(8), 633-635 (1986).
    • (1986) Eur.Polym.J. , vol.22 , Issue.8 , pp. 633-635
    • Knaub, P.1    Camberlin, Y.2
  • 185
    • 77049120309 scopus 로고    scopus 로고
    • Castor oil as a renewable resource for the chemical industry
    • H. Mutlu and M.A.R. Meier, Castor oil as a renewable resource for the chemical industry. Eur. J. Lipid Sci. Technol. 112, 10-30 (2010).
    • (2010) Eur. J. Lipid Sci. Technol. , vol.112 , pp. 10-30
    • Mutlu, H.1    Meier, M.A.R.2
  • 186
    • 0021412253 scopus 로고
    • Preparation and properties of castor oil based polyurethanes
    • Z. Petrovic and D. Fajnik, Preparation and properties of castor oil based polyurethanes. J. Appl. Polym. Sci. 29, 1031-1040 (1984).
    • (1984) J. Appl. Polym. Sci. , vol.29 , pp. 1031-1040
    • Petrovic, Z.1    Fajnik, D.2
  • 187
    • 84858631552 scopus 로고
    • Polyurethane coatings from castor oil
    • S.K. Menon and S.R. Srinivasan, Polyurethane coatings from castor oil. Paintindia 34(6), 7-12 (1984).
    • (1984) Paintindia , vol.34 , Issue.6 , pp. 7-12
    • Menon, S.K.1    Srinivasan, S.R.2
  • 188
    • 0010177638 scopus 로고    scopus 로고
    • Electroinsulating polyurethane casting resins based on soy oil and castor oil
    • SPI, Polyurethane Division, Dallas, TX
    • Z.S. Petrovic, I. Javni, and A. Guo, Electroinsulating Polyurethane Casting Resins Based on Soy Oil and Castor Oil, in Polyurethanes EXPO'98, pp. 559-562. SPI, Polyurethane Division, Dallas, TX (1998).
    • (1998) Polyurethanes EXPO'98 , pp. 559-562
    • Petrovic, Z.S.1    Javni, I.2    Guo, A.3
  • 189
    • 84951657960 scopus 로고
    • New castor oil-based urethane elastomers
    • C.K. Lyon and V.H. Garrett, New castor oil-based urethane elastomers. J. Am. Oil Chem. Soc. 50, 112 (1973).
    • (1973) J. Am. Oil Chem. Soc. , vol.50 , pp. 112
    • Lyon, C.K.1    Garrett, V.H.2
  • 190
    • 84913210457 scopus 로고
    • Diisocyanate coatings based on castor oil
    • G.C. Toone and G.S. Wooster, Diisocyanate coatings based on castor oil. Ind. Eng. Chem. Prod. Res. Dev. 51(11), 1384-1385 (1959).
    • (1959) Ind. Eng. Chem. Prod. Res. Dev. , vol.51 , Issue.11 , pp. 1384-1385
    • Toone, G.C.1    Wooster, G.S.2
  • 191
    • 0026839615 scopus 로고
    • The effect of castor-oil on the structure and properties of polyurethane elastomers
    • P.K. Saxena, S.R. Srinivasan, J. Hrouz, and M. Ilavsky, The effect of castor-oil on the structure and properties of polyurethane elastomers. J. Appl. Polym. Sci. 44(8), 1343-1347 (1992).
    • (1992) J. Appl. Polym. Sci. , vol.44 , Issue.8 , pp. 1343-1347
    • Saxena, P.K.1    Srinivasan, S.R.2    Hrouz, J.3    Ilavsky, M.4
  • 192
    • 33750954315 scopus 로고    scopus 로고
    • Addition polymers from natural oils-A review
    • V. Sharma and P.P. Kundu, Addition polymers from natural oils-A review. Prog. Polym. Sci. 31(11), 983-1008 (2006).
    • (2006) Prog. Polym. Sci. , vol.31 , Issue.11 , pp. 983-1008
    • Sharma, V.1    Kundu, P.P.2
  • 193
    • 0027708570 scopus 로고
    • Castor oil-glycerol blends as polyols for rigid polyurethane foams
    • S.A. Baser and D.V. Khakhar, Castor oil-glycerol blends as polyols for rigid polyurethane foams. Cell. Polym. 12(5), 390-401 (1993).
    • (1993) Cell. Polym. , vol.12 , Issue.5 , pp. 390-401
    • Baser, S.A.1    Khakhar, D.V.2
  • 195
    • 0003236686 scopus 로고
    • The modification of epoxidized oils with amines. I. The modification of epoxidized dehydrated castor oil with diamines
    • E.M. Abdel-Bary, B.M. Badran, and N.A. Ghanem, The modification of epoxidized oils with amines. I. The modification of epoxidized dehydrated castor oil with diamines. Eur. Polym. J. 11(5/6), 399-402 (1975).
    • (1975) Eur. Polym. J. , vol.11 , Issue.5-6 , pp. 399-402
    • Abdel-Bary, E.M.1    Badran, B.M.2    Ghanem, N.A.3
  • 197
    • 0020125658 scopus 로고
    • Polythiourethane polymers using castor oil tristhioglycolate as crosslinking agent
    • N.D. Ghatge and R.A.N. Murthy, Polythiourethane polymers using castor oil tristhioglycolate as crosslinking agent. J. Appl. Polym. Sci. 27(5), 1557-1563 (1982).
    • (1982) J. Appl. Polym. Sci. , vol.27 , Issue.5 , pp. 1557-1563
    • Ghatge, N.D.1    Murthy, R.A.N.2
  • 198
    • 0025603789 scopus 로고
    • Polyurethanes from 2,4-toluene diisocyanate and a mixture of castor oil and hydroxyether of bisphenol-A
    • Q. Guo, S. Fan, and Q. Zhang, Polyurethanes from 2,4-toluene diisocyanate and a mixture of castor oil and hydroxyether of bisphenol-A. Eur. Polym. J. 26(11), 1177-1180 (1990).
    • (1990) Eur. Polym. J. , vol.26 , Issue.11 , pp. 1177-1180
    • Guo, Q.1    Fan, S.2    Zhang, Q.3
  • 199
    • 0016436263 scopus 로고
    • Polyurethane casting compounds based on castor oil
    • Atlanta, GA
    • T.F. Kroplinski, Polyurethane Casting Compounds Based on Castor Oil, in SPE 33rd Annu. Tech. Conf. (ANTEC), pp. 242-245. Atlanta, GA, (1975).
    • (1975) SPE 33rd Annu. Tech. Conf. (ANTEC) , pp. 242-245
    • Kroplinski, T.F.1
  • 201
    • 50249150116 scopus 로고    scopus 로고
    • Segmented polyurethanes from vegetable oil-based polyols
    • Z.S. Petrovic, Y. Xu, and W. Zhang, Segmented polyurethanes from vegetable oil-based polyols. Polym. Preprints 48, 852-853 (2007).
    • (2007) Polym. Preprints , vol.48 , pp. 852-853
    • Petrovic, Z.S.1    Xu, Y.2    Zhang, W.3
  • 202
    • 50249129562 scopus 로고    scopus 로고
    • Morphology and properties of thermoplastic polyurethanes with dangling chains in ricinoleate-based soft segments
    • Y. Xu, Z.S. Petrovic, S. Das, and G.L. Wilkes, Morphology and properties of thermoplastic polyurethanes with dangling chains in ricinoleate-based soft segments. Polymer 49, 4248-4538 (2008).
    • (2008) Polymer , vol.49 , pp. 4248-4538
    • Xu, Y.1    Petrovic, Z.S.2    Das, S.3    Wilkes, G.L.4
  • 203
    • 84871924815 scopus 로고    scopus 로고
    • Phase structure in segmented polyurethanes having fatty acid-based soft segments
    • Z.S. Petrovic, D. Hong, I. Javni, N. Erina, F. Zhang, and J. Ilavsky, Phase structure in segmented polyurethanes having fatty acid-based soft segments. Polymer 54, 372-380 (2013).
    • (2013) Polymer , vol.54 , pp. 372-380
    • Petrovic, Z.S.1    Hong, D.2    Javni, I.3    Erina, N.4    Zhang, F.5    Ilavsky, J.6
  • 204
    • 84888001130 scopus 로고    scopus 로고
    • Novel thermoplastic polyurethane elastomers based on methyl-12-hydroxy stearate
    • L. Korugic-Karasz, (Ed.), ACS symposium series
    • O.S. Yemul and Z.S. Petrovic, Novel Thermoplastic Polyurethane Elastomers based on Methyl-12-Hydroxy Stearate, in Chapter 2 in Contemporary Science of Polymeric Materials, L. Korugic-Karasz, (Ed.), pp. 29-39, Vol. 1061, ACS symposium series, (2010).
    • (2010) Chapter 2 in Contemporary Science of Polymeric Materials , vol.1061 , pp. 29-39
    • Yemul, O.S.1    Petrovic, Z.S.2
  • 205
    • 41949136731 scopus 로고    scopus 로고
    • Production of 9-hydroxynonanoic acid from methyl oleate and conversion into lactone monomers for the synthesis of biodegradable polylactones
    • G. Liu, X. Kong, H. Wan, and S.S. Narine, Production of 9-hydroxynonanoic acid from methyl oleate and conversion into lactone monomers for the synthesis of biodegradable polylactones. Biomacromolecules 9, 949-953 (2008).
    • (2008) Biomacromolecules , vol.9 , pp. 949-953
    • Liu, G.1    Kong, X.2    Wan, H.3    Narine, S.S.4
  • 207
    • 84886295933 scopus 로고    scopus 로고
    • Vegetable oil-based hyperbranched polyols in flexible foams
    • Z.S. Petrovic and I. Cvetkovic, Vegetable oil-based hyperbranched polyols in flexible foams. Contemporary Materials III-1, 63-71 (2012).
    • (2012) Contemporary Materials , vol.3 , Issue.1 , pp. 63-71
    • Petrovic, Z.S.1    Cvetkovic, I.2
  • 208
    • 77953916847 scopus 로고    scopus 로고
    • Ethoxylated soybean polyols for polyurethanes
    • M. Ionescu, Z. Petrovic, and X. Wan, Ethoxylated soybean polyols for polyurethanes. J. Polym. Environ. 18, 1-7 (2010).
    • (2010) J. Polym. Environ. , vol.18 , pp. 1-7
    • Ionescu, M.1    Petrovic, Z.2    Wan, X.3
  • 212
    • 3543078712 scopus 로고    scopus 로고
    • Esterification and transesterification of renewable chemicals
    • H.E. Hoydonckx, D.E.D. Vos, S.A. Chavan, and P.A. Jacobs, Esterification and transesterification of renewable chemicals. Top. Catalysis 27(1-4), 83-96 (2004).
    • (2004) Top. Catalysis , vol.27 , Issue.1-4 , pp. 83-96
    • Hoydonckx, H.E.1    Vos, D.E.D.2    Chavan, S.A.3    Jacobs, P.A.4
  • 214
    • 84855857719 scopus 로고    scopus 로고
    • Synthesis of pseudo-telechelic diols by transesterification and thiol-ene coupling
    • M. Desroches, S. Caillol, R. Auvergne, and B. Boutevin, Synthesis of pseudo-telechelic diols by transesterification and thiol-ene coupling. Eur. J. Lipid Sci. Technol. 114, 84-91 (2012).
    • (2012) Eur. J. Lipid Sci. Technol. , vol.114 , pp. 84-91
    • Desroches, M.1    Caillol, S.2    Auvergne, R.3    Boutevin, B.4
  • 215
    • 0032202367 scopus 로고    scopus 로고
    • Transesterification of trimethylol propane and rapeseed oil methyl ester to environmentally acceptable lubricants
    • E. Uoskainen, Y.-Y. Linko, M. Lamsa, and T. Tervakkangas, Transesterification of trimethylol propane and rapeseed oil methyl ester to environmentally acceptable lubricants. J. Amer. Oil Chem. Soc. 75, 1557-1563 (1998).
    • (1998) J. Amer. Oil Chem. Soc. , vol.75 , pp. 1557-1563
    • Uoskainen, E.1    Linko, Y.-Y.2    Lamsa, M.3    Tervakkangas, T.4
  • 216
    • 84953250028 scopus 로고    scopus 로고
    • Germany Patent EP 1075460, DE 19819656, assigned to Henkel K.-G.a.A., Germany (February 14
    • A. Westfechtel and W. Giede, Method for producing polyolesters, Germany Patent EP 1075460, DE 19819656, assigned to Henkel K.-G.a.A., Germany (February 14, 2001).
    • (2001) Method for Producing Polyolesters
    • Westfechtel, A.1    Giede, W.2
  • 217
    • 0030249585 scopus 로고    scopus 로고
    • Applications of Nigella sativa seed lipase in oleochemical reactions
    • L. Dandik and H.A. Aksoy, Applications of Nigella sativa seed lipase in oleochemical reactions. Enzyme Microb. Technol. 19(4), 277-281 (1996).
    • (1996) Enzyme Microb. Technol. , vol.19 , Issue.4 , pp. 277-281
    • Dandik, L.1    Aksoy, H.A.2
  • 218
    • 0030148149 scopus 로고    scopus 로고
    • The catalytic activity of lipases toward hydroxy fatty acids
    • D.G. Hayes, The catalytic activity of lipases toward hydroxy fatty acids. J. Am. Oil Chem. Soc. 73(5), 543-549 (1996).
    • (1996) J. Am. Oil Chem. Soc. , vol.73 , Issue.5 , pp. 543-549
    • Hayes, D.G.1
  • 219
    • 0035385138 scopus 로고    scopus 로고
    • In-vitro enzyme catalyzed polymer synthesis
    • R.A. Gross, A. Kumar, and B. Kalra, In-vitro enzyme catalyzed polymer synthesis. Chem. Rev. 101(7), 2097-2124 (2001).
    • (2001) Chem. Rev. , vol.101 , Issue.7 , pp. 2097-2124
    • Gross, R.A.1    Kumar, A.2    Kalra, B.3
  • 220
    • 0039845379 scopus 로고    scopus 로고
    • Microbial synthesis, physical properties and biodegradability of ultre-high-molecular-weight poly[(r)-3-hydroxybutyrate
    • C. Scholz and R.A. Gross, (Eds.). ACS, Washington
    • T. Iwata, S. Kusaka, and Y. Doi, Microbial Synthesis, Physical properties and Biodegradability of Ultre-High-Molecular-Weight Poly[(R)-3-hydroxybutyrate], in Polymers from Renewable Resources-Biopolyesters and Biocatalysis, C. Scholz and R.A. Gross, (Eds.), pp. 67-76. ACS, Washington, (2000).
    • (2000) Polymers from Renewable Resources-Biopolyesters and Biocatalysis , pp. 67-76
    • Iwata, T.1    Kusaka, S.2    Doi, Y.3
  • 221
    • 45449120865 scopus 로고    scopus 로고
    • Chemoenzymatic synthesis of oleic acid-based polyesters for use as highly stable biomaterials
    • S. Miao, S. Zhang, Z. Su, and P. Wang, Chemoenzymatic synthesis of oleic acid-based polyesters for use as highly stable biomaterials. J. Polym. Sci. Part A Polym. Chem. 46(12), 4243-4248 (2008).
    • (2008) J. Polym. Sci. Part A Polym. Chem. , vol.46 , Issue.12 , pp. 4243-4248
    • Miao, S.1    Zhang, S.2    Su, Z.3    Wang, P.4
  • 222
    • 0032337485 scopus 로고    scopus 로고
    • Transesterification of vegetable oils: A review
    • U. Schuchardt, R. Sercheli, and R.M. Vargas, Transesterification of vegetable oils: A review. J. Bras. Chem. Soc. 9(3), 199-210 (1998).
    • (1998) J. Bras. Chem. Soc. , vol.9 , Issue.3 , pp. 199-210
    • Schuchardt, U.1    Sercheli, R.2    Vargas, R.M.3
  • 223
    • 0031122639 scopus 로고    scopus 로고
    • Optimization of the sulfuric acid-catalyzed estolide synthesisfrom oleic acid
    • T.A. Isbell, H.B. Frykman, T.P. Abbott, J.E. Lohr, and J. Drozd, Optimization of the sulfuric acid-catalyzed estolide synthesisfrom oleic acid. J. Am. Oil Chem. Soc. 74, 473-476 (1997).
    • (1997) J. Am. Oil Chem. Soc. , vol.74 , pp. 473-476
    • Isbell, T.A.1    Frykman, H.B.2    Abbott, T.P.3    Lohr, J.E.4    Drozd, J.5
  • 224
    • 0028406351 scopus 로고
    • Characterization of estolides produced from the acid-catalyzed condensation of oleic acid
    • T.A. Isbell and R. Kleiman, Characterization of estolides produced from the acid-catalyzed condensation of oleic acid. J. Am. Oil Chem. Soc. 71 (4), 379-383 (1994).
    • (1994) J. Am. Oil Chem. Soc. , vol.71 , Issue.4 , pp. 379-383
    • Isbell, T.A.1    Kleiman, R.2
  • 225
    • 0030243903 scopus 로고    scopus 로고
    • Mineral acid-catalyzed condensation of meadowfoam fatty acids into estolides
    • T.A. Isbell and R. Kleiman, Mineral acid-catalyzed condensation of meadowfoam fatty acids into estolides. J. Am. Oil Chem. Soc. 73, 1097-1107 (1996).
    • (1996) J. Am. Oil Chem. Soc. , vol.73 , pp. 1097-1107
    • Isbell, T.A.1    Kleiman, R.2
  • 226
    • 51249182223 scopus 로고
    • Hydroxy acids and estolide triglycerides of heliophila amplexicaulis L.F. Seed oil
    • R.D. Plattner, K. Payne-Wahl, L.W. Tjarks, and R. Kleiman, Hydroxy acids and estolide triglycerides of heliophila amplexicaulis L.f. seed oil. Lipids 14, 576-579 (1979).
    • (1979) Lipids , vol.14 , pp. 576-579
    • Plattner, R.D.1    Payne-Wahl, K.2    Tjarks, L.W.3    Kleiman, R.4
  • 227
    • 0020749402 scopus 로고
    • Quantitation of estolide triglycerides in sapium seeds by high-performance liquid chromatography with infrared detection
    • K. Payne-Wahl and R. Kleiman, Quantitation of estolide triglycerides in sapium seeds by high-performance liquid chromatography with infrared detection. J. Am. Oil Chem. Soc. 60, 1011-1012 (1983).
    • (1983) J. Am. Oil Chem. Soc. , vol.60 , pp. 1011-1012
    • Payne-Wahl, K.1    Kleiman, R.2
  • 228
    • 0035358486 scopus 로고    scopus 로고
    • Synthesis of estolides from oleic and saturated fatty acids
    • S.C. Cermak and T.A. Isbell, Synthesis of estolides from oleic and saturated fatty acids. J. Am. Oil Chem. Soc. 78, 557-565 (2001).
    • (2001) J. Am. Oil Chem. Soc. , vol.78 , pp. 557-565
    • Cermak, S.C.1    Isbell, T.A.2
  • 229
    • 0027588767 scopus 로고
    • Estolides from meadowfoam oil fatty acids and other monounsaturated fatty acids
    • S.M. Erhan, R. Kleiman, and T.A. Isbell, Estolides from meadowfoam oil fatty acids and other monounsaturated fatty acids. J. Am. Oil Chem. Soc. 70, 461-465 (1993).
    • (1993) J. Am. Oil Chem. Soc. , vol.70 , pp. 461-465
    • Erhan, S.M.1    Kleiman, R.2    Isbell, T.A.3
  • 230
    • 56649112940 scopus 로고    scopus 로고
    • Synthesis and physical properties of mono-estolides with varying chain lengths
    • S.C. Cermak and T.A. Isbell, Synthesis and physical properties of mono-estolides with varying chain lengths. Ind. Crops Prod. 29(1), 205-213 (2009).
    • (2009) Ind. Crops Prod. , vol.29 , Issue.1 , pp. 205-213
    • Cermak, S.C.1    Isbell, T.A.2
  • 231
    • 0036716613 scopus 로고    scopus 로고
    • Physical properties of saturated estolides and their 2-ethylhexyl esters
    • S.C. Cermak and T.A. Isbell, Physical properties of saturated estolides and their 2-ethylhexyl esters. Ind. Crops Prod. 16(2), 119-127 (2002).
    • (2002) Ind. Crops Prod. , vol.16 , Issue.2 , pp. 119-127
    • Cermak, S.C.1    Isbell, T.A.2
  • 232
    • 19244376245 scopus 로고    scopus 로고
    • Natural estolides produced by pseudomonas sp. 42A2 grown on oleic acid: Production and characterization
    • M. Peláez, C. Orellana, A. Marqués, M. Busquets, A. Guerrero, and A. Manresa, Natural estolides produced by pseudomonas sp. 42A2 grown on oleic acid: Production and characterization. J. Am. Oil Chem. Soc. 80(9), 859-866 (2003).
    • (2003) J. Am. Oil Chem. Soc. , vol.80 , Issue.9 , pp. 859-866
    • Peláez, M.1    Orellana, C.2    Marqués, A.3    Busquets, M.4    Guerrero, A.5    Manresa, A.6
  • 233
    • 61349198353 scopus 로고    scopus 로고
    • Influence of the operating conditions on lipase-catalysed synthesis of ricinoleic acid estolides in solvent-free systems
    • A. Bódalo, J. Bastida, M.F. Máximo, M.C. Montiel, M.D. Murcia, and S. Ortega, Influence of the operating conditions on lipase-catalysed synthesis of ricinoleic acid estolides in solvent-free systems. Biochem. Eng. J. 44(2-3), 214-219 (2009).
    • (2009) Biochem. Eng. J. , vol.44 , Issue.2-3 , pp. 214-219
    • Bódalo, A.1    Bastida, J.2    Máximo, M.F.3    Montiel, M.C.4    Murcia, M.D.5    Ortega, S.6
  • 236
    • 0028381702 scopus 로고
    • Acid-catalyzed condensation of oleic acid into estolides and polyestolides
    • T.A. Isbell, R. Kleiman, and B.A. Plattner, Acid-catalyzed condensation of oleic acid into estolides and polyestolides. J. Am. Oil Chem. Soc. 71, 169-174 (1994).
    • (1994) J. Am. Oil Chem. Soc. , vol.71 , pp. 169-174
    • Isbell, T.A.1    Kleiman, R.2    Plattner, B.A.3
  • 237
    • 49649119635 scopus 로고    scopus 로고
    • Comparison of a new estolide oxidative stability package
    • C. Cermak, G. Biresaw, and T.A. Isbell, Comparison of a new estolide oxidative stability package. J. Am. Chem. Soc. 85(9), 879-885 (2008).
    • (2008) J. Am. Chem. Soc. , vol.85 , Issue.9 , pp. 879-885
    • Cermak, C.1    Biresaw, G.2    Isbell, T.A.3
  • 238
    • 51249188764 scopus 로고
    • The mechanism of the aqueous perchloric acid isomerization of oleic acid to ã-stearolactone
    • I. Shepherd and J.S. Showell, The mechanism of the aqueous perchloric acid isomerization of oleic acid to ã-stearolactone. J. Am. Oil Chem. Soc. 46(9), 479-481 (1969).
    • (1969) J. Am. Oil Chem. Soc. , vol.46 , Issue.9 , pp. 479-481
    • Shepherd, I.1    Showell, J.S.2
  • 239
    • 0033891145 scopus 로고    scopus 로고
    • Synthesis of ä-stearolactone from oleic acid
    • S. Cermak and T.A. Isbell, Synthesis of ä-stearolactone from oleic acid. J. Am. Oil Chem. Soc. 77, 243-248 (2000).
    • (2000) J. Am. Oil Chem. Soc. , vol.77 , pp. 243-248
    • Cermak, S.1    Isbell, T.A.2
  • 240
    • 0034475072 scopus 로고    scopus 로고
    • 5-Hydroxy fatty acid amides from ä-lactones and alkyl glucamines
    • H.B. Frykman, T. Isbell, and S.C. Cermak, 5-Hydroxy fatty acid amides from ä-lactones and alkyl glucamines. J. Surfact. Deterg. 3(2), 179-183 (2000).
    • (2000) J. Surfact. Deterg. , vol.3 , Issue.2 , pp. 179-183
    • Frykman, H.B.1    Isbell, T.2    Cermak, S.C.3
  • 241
    • 84953318208 scopus 로고
    • Low VOC fast air-drying alkyd coatings.II. Allylic reactive diluents
    • I. Badou and S. Dirlikov, Low VOC fast air-drying alkyd coatings.II. allylic reactive diluents. Abstr. Pap. Am. Chem. Soc. 207, 178-PMSE (1994).
    • (1994) Abstr. Pap. Am. Chem. Soc. , vol.207 , pp. 178PMSE
    • Badou, I.1    Dirlikov, S.2
  • 242
    • 38949196580 scopus 로고
    • About the usage of polyhydroxyl oligomers in the synthesis of alkyd resins by transesterification with triglycerides
    • Lugano
    • T. Domide and M. Rosetti, About the usage of polyhydroxyl oligomers in the synthesis of alkyd resins by transesterification with triglycerides, in FATIPEC Congress, pp. 193-211, Vol. 17, Lugano, (1984).
    • (1984) FATIPEC Congress , vol.17 , pp. 193-211
    • Domide, T.1    Rosetti, M.2
  • 243
    • 84953266341 scopus 로고
    • Low VOC fast air-drying alkyd coatings.I. (Meth)Acrylic reactive diluents
    • C.P. Kuo, Z. Chen, N. Lathia, and S. Dirlikov, Low VOC fast air-drying alkyd coatings.I. (Meth)Acrylic reactive diluents. Abstr. Pap. Am. Chem. Soc. 207, 33-PMSE (1994).
    • (1994) Abstr. Pap. Am. Chem. Soc. , vol.207 , pp. 33PMSE
    • Kuo, C.P.1    Chen, Z.2    Lathia, N.3    Dirlikov, S.4
  • 246
    • 77955136647 scopus 로고
    • Vernonia and epoxidized linseed and soybean oils as low yellowing diluents in alkyd coatings
    • P. Muturi-Mwangi, S. Dirlikov, and P.M. Gitu, Vernonia and epoxidized linseed and soybean oils as low yellowing diluents in alkyd coatings. Pigment Resin Technol. 23(3), 3-7 (1994).
    • (1994) Pigment Resin Technol. , vol.23 , Issue.3 , pp. 3-7
    • Muturi-Mwangi, P.1    Dirlikov, S.2    Gitu, P.M.3
  • 247
    • 0022915179 scopus 로고
    • Solution parameters of linseed oil alkyd: Their dependence on solutesolvent interactions
    • M.V.R. Mohan Rao and M. Yaseen, Solution parameters of linseed oil alkyd: Their dependence on solutesolvent interactions. J. Coat. Technol. 58(743), 49-56 (1986).
    • (1986) J. Coat. Technol. , vol.58 , Issue.743 , pp. 49-56
    • Mohan Rao, M.V.R.1    Yaseen, M.2
  • 248
    • 84953233047 scopus 로고    scopus 로고
    • Reactive applications of cyclic alkylene carbonates
    • J.H. Clements, Reactive applications of cyclic alkylene carbonates, in Huntsman Technical Paper, pp. 1-12, (2002).
    • (2002) Huntsman Technical Paper , pp. 1-12
    • Clements, J.H.1
  • 249
    • 77955684577 scopus 로고    scopus 로고
    • Organic carbonates as solvents in synthesis and catalysis
    • B. Schaffner, F. Schaffner, S.P. Verevkin, and A. Borner, Organic carbonates as solvents in synthesis and catalysis. Chem. Rev. 110, 4554-4581 (2010).
    • (2010) Chem. Rev. , vol.110 , pp. 4554-4581
    • Schaffner, B.1    Schaffner, F.2    Verevkin, S.P.3    Borner, A.4
  • 251
    • 0142027127 scopus 로고    scopus 로고
    • Synthesis of modern synthetic oils based on dialkyl carbonates
    • S. Gryglewicz, F.A. Oko, and G. Gryglewicz, Synthesis of modern synthetic oils based on dialkyl carbonates. Ind. Eng. Chem. Res. 42, 5007-5010 (2003).
    • (2003) Ind. Eng. Chem. Res. , vol.42 , pp. 5007-5010
    • Gryglewicz, S.1    Oko, F.A.2    Gryglewicz, G.3
  • 252
    • 2042494991 scopus 로고
    • US Patent 5, 387, 374, assigned to Henkel Kommanditgesellschaft auf Aktien ( February 7
    • A. Westfechtel, F. Bongardt, and A. Ansmann, Guerbet Carbonates, US Patent 5,387,374, assigned to Henkel Kommanditgesellschaft auf Aktien (February 7, 1995).
    • (1995) Guerbet Carbonates
    • Westfechtel, A.1    Bongardt, F.2    Ansmann, A.3
  • 255
    • 0038240565 scopus 로고    scopus 로고
    • Production of diethyl carbonate from ethanol and carbon monoxide over a heterogeneous catalytic flow reactor
    • N.-S. Roh, B.C. Dunn, E.M. Eyring, R.J. Pugmire, and H.L.C. Meuzelaar, Production of diethyl carbonate from ethanol and carbon monoxide over a heterogeneous catalytic flow reactor. Fuel Process Technol. 83, 27-38 (2003).
    • (2003) Fuel Process Technol. , vol.83 , pp. 27-38
    • Roh, N.-S.1    Dunn, B.C.2    Eyring, E.M.3    Pugmire, R.J.4    Meuzelaar, H.L.C.5
  • 256
    • 0035560834 scopus 로고    scopus 로고
    • Developments in the production and application of dimethylcarbonate
    • D. Delledonne, F. Rivetti, and U. Romano, Developments in the production and application of dimethylcarbonate. Appl. Cat. A Gen. 221, 241-251 (2001).
    • (2001) Appl. Cat. A Gen. , vol.221 , pp. 241-251
    • Delledonne, D.1    Rivetti, F.2    Romano, U.3
  • 257
    • 5544322064 scopus 로고    scopus 로고
    • Current perspectives on oleochemical carbonates
    • J.A. Kenar, Current perspectives on oleochemical carbonates. Inform 15, 580-582 (2004).
    • (2004) Inform , vol.15 , pp. 580-582
    • Kenar, J.A.1
  • 258
    • 2042509015 scopus 로고    scopus 로고
    • Synthesis and characterization of dialkyl carbonates prepared from mid-, long-chain, and guerbet alcohols
    • J.A. Kenar, G. Knothe, and A.L. Copes, Synthesis and characterization of dialkyl carbonates prepared from mid-, long-chain, and guerbet alcohols. J. Am. Oil Chem. Soc. 81, 285-291 (2004).
    • (2004) J. Am. Oil Chem. Soc. , vol.81 , pp. 285-291
    • Kenar, J.A.1    Knothe, G.2    Copes, A.L.3
  • 260
    • 33947116363 scopus 로고    scopus 로고
    • New hyperbranched polyether containing cyclic carbonate groups as a toughening agent for epoxy resin
    • P.G. Parzuchowski, M. Kizlinska, and G. Rokicki, New hyperbranched polyether containing cyclic carbonate groups as a toughening agent for epoxy resin. Polymer 48, 1857-1865 (2007).
    • (2007) Polymer , vol.48 , pp. 1857-1865
    • Parzuchowski, P.G.1    Kizlinska, M.2    Rokicki, G.3
  • 261
    • 0026844990 scopus 로고
    • Dialkyl and diaryl carbonates by carbonate interchange reaction with dimethyl carbonate
    • A.A.G. Shaikh and S. Sivaram, Dialkyl and diaryl carbonates by carbonate interchange reaction with dimethyl carbonate. Ind. Eng. Chem. Res. 31(4), 1167-1170 (1992).
    • (1992) Ind. Eng. Chem. Res. , vol.31 , Issue.4 , pp. 1167-1170
    • Shaikh, A.A.G.1    Sivaram, S.2
  • 264
    • 15944387352 scopus 로고    scopus 로고
    • Convenient preparation of fatty ester cyclic carbonates
    • J.A. Kenar and I.D. Tevis, Convenient preparation of fatty ester cyclic carbonates. Eur. J. Lipid Sci. Technol. 107, 135-137 (2005).
    • (2005) Eur. J. Lipid Sci. Technol. , vol.107 , pp. 135-137
    • Kenar, J.A.1    Tevis, I.D.2
  • 268
    • 1642289722 scopus 로고    scopus 로고
    • Incorporation of carbon dioxide into soybean oil and subsequent preparation and studies of nonisocyanate polyurethane networks
    • B. Tamami, S. Sohn, G.L. Wilkes, and B. Tamami, Incorporation of carbon dioxide into soybean oil and subsequent preparation and studies of nonisocyanate polyurethane networks. J. Appl. Polym. Sci. 92, 883-891 (2004).
    • (2004) J. Appl. Polym. Sci. , vol.92 , pp. 883-891
    • Tamami, B.1    Sohn, S.2    Wilkes, G.L.3    Tamami, B.4
  • 270
    • 55849144428 scopus 로고    scopus 로고
    • Soy-based polyurethanes by non-isocyanate route
    • I. Javni, D.-P. Hong, and Z.S. Petrovic, Soy-based polyurethanes by non-isocyanate route. J. Appl. Polym. Sci. 108, 3876-3875 (2008).
    • (2008) J. Appl. Polym. Sci. , vol.108 , pp. 3876-4875
    • Javni, I.1    Hong, D.-P.2    Petrovic, Z.S.3
  • 272
    • 25844440993 scopus 로고    scopus 로고
    • Improved synthesis of carbonated soybean oil in supercritical carbon dioxide
    • Presented at the San Diego, CA, (unpublished)
    • K.M. Doll and S. Erhan, Improved synthesis of carbonated soybean oil in supercritical carbon dioxide, Presented at the 229th American Chemical Society National Meeting San Diego, CA, (2005) (unpublished).
    • (2005) 229th American Chemical Society National Meeting
    • Doll, K.M.1    Erhan, S.2
  • 273
    • 29144498000 scopus 로고    scopus 로고
    • The improved synthesis of carbonated soybean oil using supercritical carbon dioxide at a reduced reaction time
    • K.M. Doll and S.Z. Erhan, The improved synthesis of carbonated soybean oil using supercritical carbon dioxide at a reduced reaction time. Green Chem. 7, 849-854 (2005).
    • (2005) Green Chem. , vol.7 , pp. 849-854
    • Doll, K.M.1    Erhan, S.Z.2
  • 274
    • 33845957553 scopus 로고    scopus 로고
    • Solventless synthesis of cyclic carbonates from carbon dioxide and epoxides catalyzed by silica-supported ionic liquids under supercritical conditions
    • J.-Q. Wang, Xiao-Dong Yue, F. Cai, and L.-N. He, Solventless synthesis of cyclic carbonates from carbon dioxide and epoxides catalyzed by silica-supported ionic liquids under supercritical conditions. Catal. Commun. 8, 167-172 (2007).
    • (2007) Catal. Commun. , vol.8 , pp. 167-172
    • Wang, J.-Q.1    Xiao-Dong, Yue.2    Cai, F.3    He, L.-N.4
  • 275
    • 22944443596 scopus 로고    scopus 로고
    • Development in the green synthesis of cyclic carbonate from carbon dioxide using ionic liquids
    • J. Sun, S.-i. Fujita, and M. Arai, Development in the green synthesis of cyclic carbonate from carbon dioxide using ionic liquids. J. Organomet. Chem. 690(15), 3490-3497 (2005).
    • (2005) J. Organomet. Chem. , vol.690 , Issue.15 , pp. 3490-3497
    • Sun, J.1    Fujita, S.-I.2    Arai, M.3
  • 276
    • 0025861064 scopus 로고
    • First lipasecatalyzed synthesis of fatty carbonate esters
    • D. Pioch, P. Lozano, and J. Graille, First lipasecatalyzed synthesis of fatty carbonate esters. Biotechnol. Lett. 13(9), 633-636 (1991).
    • (1991) Biotechnol. Lett. , vol.13 , Issue.9 , pp. 633-636
    • Pioch, D.1    Lozano, P.2    Graille, J.3
  • 277
    • 0026649234 scopus 로고
    • Vinyl carbonates as novel alkoxycarbonylation reagents in enzymatic synthesis of carbonates
    • M. Poza, R. Pulido, and V. Gotor, Vinyl carbonates as novel alkoxycarbonylation reagents in enzymatic synthesis of carbonates. Tetrahedron 48, 6477-6484 (1992).
    • (1992) Tetrahedron , vol.48 , pp. 6477-6484
    • Poza, M.1    Pulido, R.2    Gotor, V.3
  • 278
    • 84953325938 scopus 로고    scopus 로고
    • US Patent 5, 679,871 assigned to Reichhold Chemicals, Inc.October 21
    • H. Nava, Hydroxyalklylation of phenols, US Patent 5,679,871 assigned to Reichhold Chemicals, Inc. (October 21, 1997).
    • (1997) Hydroxyalklylation of Phenols
    • Nava, H.1
  • 280
    • 22144432663 scopus 로고    scopus 로고
    • Zeolitebased organic-inorganic hybrid catalysts for phosgene free and solvent free synthesis of cyclic carbonates and carbamates at mild conditions utilizing CO2
    • R. Srinistava, D. Srinivas, and P. Ratnaswami, Zeolitebased organic-inorganic hybrid catalysts for phosgene free and solvent free synthesis of cyclic carbonates and carbamates at mild conditions utilizing CO2. Appl. Catalysis A Gen. 289, 128-134 (2005).
    • (2005) Appl. Catalysis A Gen. , vol.289 , pp. 128-134
    • Srinistava, R.1    Srinivas, D.2    Ratnaswami, P.3
  • 282
    • 33747826604 scopus 로고    scopus 로고
    • Transesterification of cyclic carbonates with methanol at ambient conditions over tungstatebased solid catalysts
    • M. Sankar, N. Madhavan, M.C. , K.V.G.K. Murty, and P. Manikandan, Transesterification of cyclic carbonates with methanol at ambient conditions over tungstatebased solid catalysts. Appl. Catalysis A Gen. 312, 108-114 (2006).
    • (2006) Appl. Catalysis A Gen. , vol.312 , pp. 108-114
    • Sankar, M.1    Madhavan, N.2    Murty, K.V.G.K.3    Manikandan, P.4
  • 285
    • 0037128531 scopus 로고    scopus 로고
    • A new route to polyurethanes from ethylene carbonate, diamines and diols
    • G. Rokicki and A. Piotrowska, A new route to polyurethanes from ethylene carbonate, diamines and diols. Polymer 43, 2927-2935 (2002).
    • (2002) Polymer , vol.43 , pp. 2927-2935
    • Rokicki, G.1    Piotrowska, A.2
  • 286
    • 0036036691 scopus 로고    scopus 로고
    • Features of reaction amino-cyclocarbonate for production of new type nonisocyanate polyurethane coatings
    • O.L. Figovsky and L.D. Shapovalov, Features of reaction amino-cyclocarbonate for production of new type nonisocyanate polyurethane coatings. Macromol. Symp. 187, 325-332 (2002).
    • (2002) Macromol. Symp. , vol.187 , pp. 325-332
    • Figovsky, O.L.1    Shapovalov, L.D.2
  • 287
    • 4544267190 scopus 로고    scopus 로고
    • Copolymers and terpolymers of Tetramethylene Urea, ã-Butyrolactone, and Ethylene carbonate or 1,2-propylene carbonate
    • L. Ubaghs, M. Waringo, H. Keul, and H. Hocker, Copolymers and terpolymers of Tetramethylene Urea, ã-Butyrolactone, and Ethylene carbonate or 1,2-propylene carbonate. Macromolecules 37, 6755-6762 (2004).
    • (2004) Macromolecules , vol.37 , pp. 6755-6762
    • Ubaghs, L.1    Waringo, M.2    Keul, H.3    Hocker, H.4
  • 288
    • 0035850615 scopus 로고    scopus 로고
    • Syntheses and thermal properties of poly(hydroxy)urethanes by polyaddition reaction of bis(cyclic carbonate) and diamines
    • M.-R. Kim, H.-S. Kim, C.-S. Ha, D.-W. Park, and J.-K. Lee, Syntheses and thermal properties of poly(hydroxy)urethanes by polyaddition reaction of bis(cyclic carbonate) and diamines. J. Appl. Polym. Sci. 81, 2735-2743 (2001).
    • (2001) J. Appl. Polym. Sci. , vol.81 , pp. 2735-2743
    • Kim, M.-R.1    Kim, H.-S.2    Ha, C.-S.3    Park, D.-W.4    Lee, J.-K.5
  • 289
    • 0033718936 scopus 로고    scopus 로고
    • Addition of five-membered cyclic carbonate with amine and its application to polymer synthesis
    • A. Steblyanko, W. Choi, F. Sanda, and T. Endo, Addition of five-membered cyclic carbonate with amine and its application to polymer synthesis. J. Polym. Sci. Part A Polym. Chem. 38, 2375-2380 (2000).
    • (2000) J. Polym. Sci. Part A Polym. Chem. , vol.38 , pp. 2375-2380
    • Steblyanko, A.1    Choi, W.2    Sanda, F.3    Endo, T.4
  • 290
    • 84872328017 scopus 로고    scopus 로고
    • Polyurethanes from soybean oil, aromatic and cycloaliphatic diamines by non-isocyanate route
    • I. Javni, D. Hong, and Z.S. Petrovic, Polyurethanes from soybean oil, aromatic and cycloaliphatic diamines by non-isocyanate route. J. Appl. Polym. Sci. 128(1), 566-571 (2013).
    • (2013) J. Appl. Polym. Sci. , vol.128 , Issue.1 , pp. 566-571
    • Javni, I.1    Hong, D.2    Petrovic, Z.S.3
  • 291
    • 84857153508 scopus 로고    scopus 로고
    • Linseed and soybean oilbased polyurethanes prepared via the non-isocyanate route and catalytic carbon dioxide conversion
    • M. Bähr and R. Mülhaupt, Linseed and soybean oilbased polyurethanes prepared via the non-isocyanate route and catalytic carbon dioxide conversion. Green Chem. 14, 483-489 (2012).
    • (2012) Green Chem. , vol.14 , pp. 483-489
    • Bähr, M.1    Mülhaupt, R.2
  • 292
    • 84860485268 scopus 로고    scopus 로고
    • Cyclic limonene dicarbonate as a new monomer for non-isocyanate oligo-and polyurethanes (NIPU) based upon terpenes
    • M. Bähr, A. Bitto, and R. Mulhaupt, Cyclic limonene dicarbonate as a new monomer for non-isocyanate oligo-and polyurethanes (NIPU) based upon terpenes. Green Chem. 14, 1447-1454 (2012).
    • (2012) Green Chem. , vol.14 , pp. 1447-1454
    • Bähr, M.1    Bitto, A.2    Mulhaupt, R.3
  • 293
    • 84982344767 scopus 로고
    • Mechanism of ozonolysis
    • R. Criegee, Mechanism of ozonolysis. Angew. Chem. Int. Ed. Engl. 14(11), 745-752 (1975).
    • (1975) Angew. Chem. Int. Ed. Engl. , vol.14 , Issue.11 , pp. 745-752
    • Criegee, R.1
  • 294
    • 45249113717 scopus 로고    scopus 로고
    • Ozonolysis in solvent/water mixtures: Direct conversion of alkenes to aldehydes and ketones
    • C.E. Schiaffo and P.H. Dussault, Ozonolysis in solvent/water mixtures: Direct conversion of alkenes to aldehydes and ketones. J. Org. Chem. 73, 4688-4690 (2008).
    • (2008) J. Org. Chem. , vol.73 , pp. 4688-4690
    • Schiaffo, C.E.1    Dussault, P.H.2
  • 295
    • 33947393011 scopus 로고    scopus 로고
    • Ozone-mediated polyol synthesis from soybean oil
    • P. Tran, D. Graiver, and R. Narayan, Ozone-mediated polyol synthesis from soybean oil. JAOCS 82(9), 653-659 (2005).
    • (2005) JAOCS , vol.82 , Issue.9 , pp. 653-659
    • Tran, P.1    Graiver, D.2    Narayan, R.3
  • 297
    • 0942268463 scopus 로고    scopus 로고
    • Synthesis and polymerization of the bromoacrylated plant oil triglycerides to rigid, flame retardant polymers
    • T. Eren and S.H. Küsefoglu, Synthesis and polymerization of the bromoacrylated plant oil triglycerides to rigid, flame retardant polymers. J. Appl. Polym. Sci. 91, 2700-2710 (2004).
    • (2004) J. Appl. Polym. Sci. , vol.91 , pp. 2700-2710
    • Eren, T.1    Küsefoglu, S.H.2
  • 299
    • 30344487652 scopus 로고    scopus 로고
    • Polyester networks based upon epoxidized and maleinated natural oils
    • H. Warth, R. Muelhaupt, B. Hoffmann, and S. Lawson, Polyester networks based upon epoxidized and maleinated natural oils. Angew.Makromol.Chem. 249, 79-92 (1997).
    • (1997) Angew.Makromol.Chem. , vol.249 , pp. 79-92
    • Warth, H.1    Muelhaupt, R.2    Hoffmann, B.3    Lawson, S.4
  • 302
    • 61349119908 scopus 로고    scopus 로고
    • Novel polymeric materials from vegetable oils and vinyl monomers: Preparation, properties, and applications
    • Y. Lu and R. Larock, Novel polymeric materials from vegetable oils and vinyl monomers: Preparation, properties, and applications. ChemSusChem 2(2), 136-147 (2009).
    • (2009) ChemSusChem , vol.2 , Issue.2 , pp. 136-147
    • Lu, Y.1    Larock, R.2
  • 303
    • 33644532848 scopus 로고    scopus 로고
    • Acrylated vegetable oils as photocrosslinkable materials
    • H. Pelletier, N. Belgacem, and A. Gandini, Acrylated vegetable oils as photocrosslinkable materials. J. Appl. Polym. Sci. 99, 3218-3221 (2006).
    • (2006) J. Appl. Polym. Sci. , vol.99 , pp. 3218-3221
    • Pelletier, H.1    Belgacem, N.2    Gandini, A.3
  • 305
    • 34548744598 scopus 로고    scopus 로고
    • Sheet molding compound resins from soybean oil: Thickening behaviour and mechanical properties
    • J. Lu and R.P. Wool, Sheet molding compound resins from soybean oil: Thickening behaviour and mechanical properties. Polym. Eng. Sci. 47(9), 1469-1479 (2007).
    • (2007) Polym. Eng. Sci. , vol.47 , Issue.9 , pp. 1469-1479
    • Lu, J.1    Wool, R.P.2
  • 306
    • 78650280765 scopus 로고    scopus 로고
    • Hybrid thermosets from vinyl ester resin and acrylated epoxidized soybean oil (AESO)
    • S. Grishchuk and J. Karger-Kocsis, Hybrid thermosets from vinyl ester resin and acrylated epoxidized soybean oil (AESO). Exp. Polym. Lett. 5(1), 2-11 (2011).
    • (2011) Exp. Polym. Lett. , vol.5 , Issue.1 , pp. 2-11
    • Grishchuk, S.1    Karger-Kocsis, J.2
  • 309
    • 33744823004 scopus 로고    scopus 로고
    • Preparation of acrylated and urethanated triacylglycerols
    • H. Pelletier and A. Gandini, Preparation of acrylated and urethanated triacylglycerols. Eur. J. Lipid Sci. Technol. 108(5 ), 411-420 (2006).
    • (2006) Eur. J. Lipid Sci. Technol. , vol.108 , Issue.5 , pp. 411-420
    • Pelletier, H.1    Gandini, A.2
  • 310
    • 25444474525 scopus 로고    scopus 로고
    • Synthesis and polymerization of the acrylamide derivatives of fatty compounds
    • T. Eren and S.H. Kusefoglu, Synthesis and polymerization of the acrylamide derivatives of fatty compounds. J. Appl. Polym. Sci. 97(6), 2264-2272 (2005).
    • (2005) J. Appl. Polym. Sci. , vol.97 , Issue.6 , pp. 2264-2272
    • Eren, T.1    Kusefoglu, S.H.2
  • 311
    • 79551693767 scopus 로고    scopus 로고
    • Chain transfer of vegetable oil macromonomers in acrylic solution copolymerization
    • M. Black, J. Messman, and J. Rawlins, Chain transfer of vegetable oil macromonomers in acrylic solution copolymerization. J. Appl. Polym. Sci. 120(3), 390-1396 (2011).
    • (2011) J. Appl. Polym. Sci. , vol.120 , Issue.3 , pp. 390-1396
    • Black, M.1    Messman, J.2    Rawlins, J.3
  • 312
    • 60649104917 scopus 로고    scopus 로고
    • A new route to acrylate oils: Crosslinking and properties of acrylate triglycerides from high oleic sunflower oil
    • L. Montero de Espinosa, J.C. Ronda, M. Galia, and V. Cádiz, A new route to acrylate oils: Crosslinking and properties of acrylate triglycerides from high oleic sunflower oil. J. Polym. Sci. Part A Polym. Chem. 47(4), 1159-1167 (2009).
    • (2009) J. Polym. Sci. Part A Polym. Chem. , vol.47 , Issue.4 , pp. 1159-1167
    • Montero De Espinosa, L.1    Ronda, J.C.2    Galia, M.3    Cádiz, V.4
  • 313
    • 10044274361 scopus 로고    scopus 로고
    • Property analysis of triglyceride-based thermosets
    • J.J. La Scala and R.P. Wool, Property analysis of triglyceride-based thermosets. Polymer 46(1), 61-69 (2005).
    • (2005) Polymer , vol.46 , Issue.1 , pp. 61-69
    • La Scala, J.J.1    Wool, R.P.2
  • 314
    • 35948933790 scopus 로고    scopus 로고
    • Phenol alkylation with 1-octene on solid acid catalysts
    • A. De Klerk and R.J.J. Nel, Phenol alkylation with 1-octene on solid acid catalysts. Ind. Eng. Chem. Res. 46, 7066-7072 (2007).
    • (2007) Ind. Eng. Chem. Res. , vol.46 , pp. 7066-7072
    • De Klerk, A.1    Nel, R.J.J.2
  • 315
    • 0025838450 scopus 로고
    • Alkylation of phenol with.alpha.-methylstyrene, propylene, butenes, isoamylene, 1-octene, and diisobutylene: Heterogeneous vs. Homogeneous catalysts
    • B. Chaudhuri and M.M. Sharma, Alkylation of phenol with.alpha.-methylstyrene, propylene, butenes, isoamylene, 1-octene, and diisobutylene: Heterogeneous vs. homogeneous catalysts. Ind. Eng. Chem. Res. 30, 227-231 (1991).
    • (1991) Ind. Eng. Chem. Res. , vol.30 , pp. 227-231
    • Chaudhuri, B.1    Sharma, M.M.2
  • 316
    • 33947348532 scopus 로고
    • The synthesis of phenolic long chain fatty acids
    • J.B. Niederl and C.Liota, The synthesis of phenolic long chain fatty acids. J. Am. Chem. Soc. 55, 3025-3026 (1933).
    • (1933) J. Am. Chem. Soc. , vol.55 , pp. 3025-3026
    • Niederl, J.B.1    Liota, C.2
  • 317
    • 0009858778 scopus 로고
    • Addition of phenols to the ethylenic linkage. The action of phenols of allyl alcohol, allyl acetate, vinyl acetate and allyl ethers
    • J.B. Niederl, R.A. Smith, and M.F. McGreal, Addition of phenols to the ethylenic linkage. the action of phenols of allyl alcohol, allyl acetate, vinyl acetate and allyl ethers. J. Am. Chem. Soc. 53(9), 3390-3396 (1931).
    • (1931) J. Am. Chem. Soc. , vol.53 , Issue.9 , pp. 3390-3396
    • Niederl, J.B.1    Smith, R.A.2    McGreal, M.F.3
  • 318
    • 33947348442 scopus 로고
    • Addition of phenols to the ethylenic linkage. Reaction mechanism and synthesis of certain phenolic ethers
    • J.B. Niederl and S. Natelson, Addition of phenols to the ethylenic linkage. reaction mechanism and synthesis of certain phenolic ethers. J. Am. Chem. Soc. 53, 272-277 (1931).
    • (1931) J. Am. Chem. Soc. , vol.53 , pp. 272-277
    • Niederl, J.B.1    Natelson, S.2
  • 319
    • 0007158841 scopus 로고
    • Improved yields in the acid catalyzed addition of phenols and phenyl ethers to oleic acid
    • W.C. Ault and A. Eisner, Improved yields in the acid catalyzed addition of phenols and phenyl ethers to oleic acid. J. Am. Oil Chem. Soc. 39, 132-133 (1962).
    • (1962) J. Am. Oil Chem. Soc. , vol.39 , pp. 132-133
    • Ault, W.C.1    Eisner, A.2
  • 321
    • 79955017876 scopus 로고    scopus 로고
    • Phenolation of vegetable oils
    • M. Ionescu and Z.S. Petrovic, Phenolation of vegetable oils. J. Serb. Chem. Soc. 76(4), 591-606 (2011).
    • (2011) J. Serb. Chem. Soc. , vol.76 , Issue.4 , pp. 591-606
    • Ionescu, M.1    Petrovic, Z.S.2
  • 322
    • 84953214301 scopus 로고    scopus 로고
    • M.Sc.Thesis Pittsburg State University
    • K.H. Hong, M.Sc.Thesis, Pittsburg State University, (2004).
    • (2004)
    • Hong, K.H.1
  • 325
    • 0021389796 scopus 로고
    • Methanesulfonic acid catalyzed addition of aromatic compounds to oleic acid
    • Y. Nakano and T.A. Foglia, Methanesulfonic acid catalyzed addition of aromatic compounds to oleic acid. J. Am. Oil Chem. Soc. 61(3), 569-573 (1984).
    • (1984) J. Am. Oil Chem. Soc. , vol.61 , Issue.3 , pp. 569-573
    • Nakano, Y.1    Foglia, T.A.2
  • 326
    • 0342694844 scopus 로고
    • Further studies on methanesulfonic acid catalyzed additions to oleic acid
    • A. Eisner, T. Perlstein, and W.C. Ault, Further studies on methanesulfonic acid catalyzed additions to oleic acid. J. Am. Oil Chem. Soc. 39, 290-292 (1962).
    • (1962) J. Am. Oil Chem. Soc. , vol.39 , pp. 290-292
    • Eisner, A.1    Perlstein, T.2    Ault, W.C.3
  • 333
    • 64549136235 scopus 로고    scopus 로고
    • Free radical addition of butanethiol to vegetable oil double bonds
    • G.B. Bantchev, J.A. Kenar, G. Biresaw, and M.G. Han, Free radical addition of butanethiol to vegetable oil double bonds. J. Agric. Food Chem. 57(4), 1281-1290 (2009).
    • (2009) J. Agric. Food Chem. , vol.57 , Issue.4 , pp. 1281-1290
    • Bantchev, G.B.1    Kenar, J.A.2    Biresaw, G.3    Han, M.G.4
  • 334
    • 33846481334 scopus 로고    scopus 로고
    • Synthesis of hydroxy thio-ether derivatives of vegetable oil
    • B.K. Sharma, A. Adhvaryu, and S.Z. Erhan, Synthesis of hydroxy thio-ether derivatives of vegetable oil. J. Agric. Food Chem. 54, 9866-9872 (2006).
    • (2006) J. Agric. Food Chem. , vol.54 , pp. 9866-9872
    • Sharma, B.K.1    Adhvaryu, A.2    Erhan, S.Z.3
  • 335
    • 79955018189 scopus 로고    scopus 로고
    • Synthesis of biobased polyols by Thiol-Ene coupling from vegetable oils
    • M. Desroches, S. Caillol, V. Lapinte, R. Auvergne, and B. Boutevin, Synthesis of biobased polyols by Thiol-Ene coupling from vegetable oils. Macromolecules 44(8), 2489-2500 (2011).
    • (2011) Macromolecules , vol.44 , Issue.8 , pp. 2489-2500
    • Desroches, M.1    Caillol, S.2    Lapinte, V.3    Auvergne, R.4    Boutevin, B.5
  • 337
    • 36749014055 scopus 로고
    • 1,3-Dipolar cycloadditions. Past and future
    • R. Huisgen, 1,3-Dipolar cycloadditions. past and future. Angew. Chem. Int. Ed. 2(10), 565-598 (1963).
    • (1963) Angew. Chem. Int. Ed. , vol.2 , Issue.10 , pp. 565-598
    • Huisgen, R.1
  • 338
    • 67649635370 scopus 로고    scopus 로고
    • Click chemistry in macromolecular science
    • T.P. Lodge, Click chemistry in macromolecular science. Macromolecules 42(12), 3827-3829 (2009).
    • (2009) Macromolecules , vol.42 , Issue.12 , pp. 3827-3829
    • Lodge, T.P.1
  • 340
    • 0037329770 scopus 로고    scopus 로고
    • Fat-derived aziridines and their N-substituted derivatives: Biologically active compounds based on renewable raw materials
    • S. Furmeier and J.O. Metzger, Fat-derived aziridines and their N-substituted derivatives: Biologically active compounds based on renewable raw materials. Eur. J. Org. Chem. 4, 649-659 (2003).
    • (2003) Eur. J. Org. Chem. , vol.4 , pp. 649-659
    • Furmeier, S.1    Metzger, J.O.2
  • 341
    • 0344980343 scopus 로고    scopus 로고
    • New type of skipped oligoaziridines: Synthesis of new fatty acid derivatives containing aziridine functions
    • J.O. Metzger and S. Fürmeier, New type of skipped oligoaziridines: Synthesis of new fatty acid derivatives containing aziridine functions. Eur. J. Org. Chem. 1999(3), 661-664 (1999).
    • (1999) Eur. J. Org. Chem. , vol.1999 , Issue.3 , pp. 661-664
    • Metzger, J.O.1    Fürmeier, S.2
  • 342
    • 0028497998 scopus 로고
    • Functionalization at the double-bond region of jojoba oil. 6. Production of amines via azides
    • V. Avidon and A. Shani, Functionalization at the double-bond region of jojoba oil. 6. Production of amines via azides. J. Am. Oil Chem. Soc. 71(9), 993-997 (1994).
    • (1994) J. Am. Oil Chem. Soc. , vol.71 , Issue.9 , pp. 993-997
    • Avidon, V.1    Shani, A.2
  • 343
    • 77952133512 scopus 로고    scopus 로고
    • Synthesis of biobased polyurethane from oleic and ricinoleic acids as the renewable resources via the AB-type self-condensation approach
    • D.V. Palaskar, A. Boyer, E. Cloutet, C. Alfos, and H. Cramail, Synthesis of biobased polyurethane from oleic and ricinoleic acids as the renewable resources via the AB-type self-condensation approach. Biomacromolecules 11(5), 1202-1211 (2010).
    • (2010) Biomacromolecules , vol.11 , Issue.5 , pp. 1202-1211
    • Palaskar, D.V.1    Boyer, A.2    Cloutet, E.3    Alfos, C.4    Cramail, H.5
  • 344
    • 84855576276 scopus 로고    scopus 로고
    • Biopolymers from vegetable oils via catalyst-and solvent-free "Click" chemistry: Effects of cross-linking density
    • J. Hong, Q. Luo, X. Wan, Z.S. Petrovic, and B.K. Shah, Biopolymers from vegetable oils via catalyst-and solvent-free "Click" chemistry: Effects of cross-linking density. Biomacromolecules 13(1), 261-266 (2012).
    • (2012) Biomacromolecules , vol.13 , Issue.1 , pp. 261-266
    • Hong, J.1    Luo, Q.2    Wan, X.3    Petrovic, Z.S.4    Shah, B.K.5
  • 345
    • 84872414525 scopus 로고    scopus 로고
    • Vegetable oil cast resins via "Click" chemistry: Effects of cross-linkers
    • J. Hong, B.K. Shah, and Z.S. Petrović, Vegetable oil cast resins via "Click" chemistry: Effects of cross-linkers. Eur. J. Lipid Chem. Technol. 115(1), 55-60 (2013).
    • (2013) Eur. J. Lipid Chem. Technol. , vol.115 , Issue.1 , pp. 55-60
    • Hong, J.1    Shah, B.K.2    Petrović, Z.S.3
  • 346
    • 0032514162 scopus 로고    scopus 로고
    • Some recent applications of olefin meta thesis in organic synthesis: A review
    • K.J. Ivin, Some recent applications of olefin metathesis in organic synthesis: A review. J. Mol. Cat. A Chem. 133, 1-16 (1998).
    • (1998) J. Mol. Cat. A Chem. , vol.133 , pp. 1-16
    • Ivin, K.J.1
  • 348
    • 0032650233 scopus 로고    scopus 로고
    • Rutheniumcatalyzed metathesis of vegetable oils
    • M.D. Refvik, R.C. Larock, and Q. Tian, Rutheniumcatalyzed metathesis of vegetable oils. JAOCS 76(1), 93-98 (1999).
    • (1999) JAOCS , vol.76 , Issue.1 , pp. 93-98
    • Refvik, M.D.1    Larock, R.C.2    Tian, Q.3
  • 349
    • 77951605904 scopus 로고    scopus 로고
    • Acyclic triene metathesis oligo-and polymerization of high oleic sun flower oil
    • U. Biermann, J.O. Metzger, and M.A.R. Meier, Acyclic triene metathesis oligo-and polymerization of high oleic sun flower oil. Macromol. Chem. Phys. 211, 854-862 (2010).
    • (2010) Macromol. Chem. Phys. , vol.211 , pp. 854-862
    • Biermann, U.1    Metzger, J.O.2    Meier, M.A.R.3
  • 351
    • 84953275446 scopus 로고
    • US Patent 4, 545, 941, assigned to A. E. Staley Manufacturing Company ( October 8
    • D.W. Rosenburg, Co-metathesis of triglycerides and ethylene, US Patent 4,545,941, assigned to A. E. Staley Manufacturing Company (October 8, 1985).
    • (1985) Co-metathesis of Triglycerides and Ethylene
    • Rosenburg, D.W.1
  • 352
    • 2442625578 scopus 로고    scopus 로고
    • Renewable monomer feedstocks via olefin meta thesis: Fundamental mechanistic studies of methyl oleate ethenolysis with the first-generation grubbs catalyst
    • K.A. Burdett, L.D. Harris, P. Margl, B.R. Maughon, T. Mokhtar-Zadeh, P.C. Saucier, and E.P. Wasserman, Renewable monomer feedstocks via olefin metathesis: Fundamental mechanistic studies of methyl oleate ethenolysis with the first-generation grubbs catalyst. Organometallics 23(9), 2027-2047 (2004).
    • (2004) Organometallics , vol.23 , Issue.9 , pp. 2027-2047
    • Burdett, K.A.1    Harris, L.D.2    Margl, P.3    Maughon, B.R.4    Mokhtar-Zadeh, T.5    Saucier, P.C.6    Wasserman, E.P.7
  • 353
    • 0028429898 scopus 로고
    • Metathesis of unsaturated fatty acid esters and fatty oils
    • J.C. Mol, Metathesis of unsaturated fatty acid esters and fatty oils. J. Mol. Catal. 90, 185-200 (1994).
    • (1994) J. Mol. Catal. , vol.90 , pp. 185-200
    • Mol, J.C.1
  • 354
    • 57649217307 scopus 로고    scopus 로고
    • Cross-metathesis reactions of allyl chloride with fatty acid methyl esters: Efficient synthesis of á,ù-difunctional chemical intermediates from renewable raw materials
    • T. Jacobs, A. Rybak, and M.A.R. Meier, Cross-metathesis reactions of allyl chloride with fatty acid methyl esters: Efficient synthesis of á,ù-difunctional chemical intermediates from renewable raw materials. Appl. Catal. A 353, 32-35 (2009).
    • (2009) Appl. Catal. A , vol.353 , pp. 32-35
    • Jacobs, T.1    Rybak, A.2    Meier, M.A.R.3
  • 355
    • 36349031081 scopus 로고    scopus 로고
    • Cross-metathesis of fatty acid derivatives with methyl acrylate: Renewable raw materials for the chemical industry
    • A. Rybak and M.A.R. Meier, Cross-metathesis of fatty acid derivatives with methyl acrylate: Renewable raw materials for the chemical industry. Green Chem. 9, 1356-1361 (2007).
    • (2007) Green Chem. , vol.9 , pp. 1356-1361
    • Rybak, A.1    Meier, M.A.R.2
  • 356
    • 79954615770 scopus 로고    scopus 로고
    • Plant oils: The perfect renewable resource for polymer science?!
    • L. Montero de Espinosa and M.A.R. Meier, Plant oils: The perfect renewable resource for polymer science?!, Eur. Polym. J. 47(5), 837-852 (2011).
    • (2011) Eur. Polym. J. , vol.47 , Issue.5 , pp. 837-852
    • Montero De Espinosa, L.1    Meier, M.A.R.2
  • 358
    • 33746917204 scopus 로고    scopus 로고
    • Metathesis of unsaturated fatty acids: Synthesis of long-chain unsaturated-Á,ù-dicarboxylic acids
    • H.L. Ngo, K. Jones, and T.A. Foglia, Metathesis of unsaturated fatty acids: Synthesis of long-chain unsaturated-á,ù-dicarboxylic acids. J. Amer. Oil Chem. Soc. 83(7), 629-634 (2006).
    • (2006) J. Amer. Oil Chem. Soc. , vol.83 , Issue.7 , pp. 629-634
    • Ngo, H.L.1    Jones, K.2    Foglia, T.A.3
  • 359
    • 51249191797 scopus 로고
    • Homogeneous catalytic metathesis of unsaturated fatty esters: New synthetic method for preparation of unsaturated mono-and dicarboxylic acids
    • P.B. Van Dam, M.C. Mittelmeijer, and C. Boelhouwer, Homogeneous catalytic metathesis of unsaturated fatty esters: New synthetic method for preparation of unsaturated mono-and dicarboxylic acids. J. Amer. Oil Chem. Soc. 51, 389-392 (1974).
    • (1974) J. Amer. Oil Chem. Soc. , vol.51 , pp. 389-392
    • Van Dam, P.B.1    Mittelmeijer, M.C.2    Boelhouwer, C.3
  • 360
    • 34248386383 scopus 로고    scopus 로고
    • Polyhydroxy fatty acids derived from sophorolipids
    • J.A. Zerkowski and D.K.Y. Solaiman, Polyhydroxy fatty acids derived from sophorolipids. J. Am. Oil Chem. Soc. 84, 463-471 (2007).
    • (2007) J. Am. Oil Chem. Soc. , vol.84 , pp. 463-471
    • Zerkowski, J.A.1    Solaiman, D.K.Y.2
  • 361
    • 0028445076 scopus 로고
    • Technological and economical aspects of the metathesis of unsaturated esters
    • M. Sibeijin, E.K. Poels, A. Bliek, and J.A. Moulijn, Technological and economical aspects of the metathesis of unsaturated esters. J. Am. Oil Chem. Soc. 71, 553-561 (1994).
    • (1994) J. Am. Oil Chem. Soc. , vol.71 , pp. 553-561
    • Sibeijin, M.1    Poels, E.K.2    Bliek, A.3    Moulijn, J.A.4
  • 362
    • 84953229892 scopus 로고    scopus 로고
    • Castor oil-based thermosets with varied crosslink densities prepared by ring-opening metathesis polymerization (romp)
    • Y. Xia and R.C. Larock, Castor oil-based thermosets with varied crosslink densities prepared by ring-opening metathesis polymerization (romp). Polym. Preprints 51(1), 765-766 (2010).
    • (2010) Polym. Preprints , vol.51 , Issue.1 , pp. 765-766
    • Xia, Y.1    Larock, R.C.2
  • 363
    • 64249153152 scopus 로고    scopus 로고
    • Novel thermosets obtained by the ring-opening metathesis polymerization of a functionalized vegetable oil and dicyclopentadiene
    • P. Henna and R.C. Larock, Novel thermosets obtained by the ring-opening metathesis polymerization of a functionalized vegetable oil and dicyclopentadiene. J. Appl. Polym. Sci. 112(3), 1788-1797 (2009).
    • (2009) J. Appl. Polym. Sci. , vol.112 , Issue.3 , pp. 1788-1797
    • Henna, P.1    Larock, R.C.2
  • 364
    • 68249159782 scopus 로고    scopus 로고
    • Metathesis with oleochemicals: New approaches for the utilization of plant oils as renewable resources in polymer science
    • M.A.R. Meier, Metathesis with oleochemicals: New approaches for the utilization of plant oils as renewable resources in polymer science. Macromol. Chem. Phys. 210, 1073-1079 (2009).
    • (2009) Macromol. Chem. Phys. , vol.210 , pp. 1073-1079
    • Meier, M.A.R.1
  • 366
    • 0032395387 scopus 로고    scopus 로고
    • Metathesis in oleochemistry
    • J.C. Mol and R. Buffon, Metathesis in oleochemistry. J. Braz. Chem. Soc. 9(1), 1-11 (1998).
    • (1998) J. Braz. Chem. Soc. , vol.9 , Issue.1 , pp. 1-11
    • Mol, J.C.1    Buffon, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.