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Volumn 48, Issue 23, 2009, Pages 10387-10394

Heterogeneously-catalyzed glycerolysis of fatty acid methyl esters: Reaction parameter optimization

Author keywords

[No Author keywords available]

Indexed keywords

BASE CATALYST; CATALYST PARTICLE SIZE; COMMERCIAL TECHNOLOGY; FATTY ACID METHYL ESTER; FOUR-PHASE; GLYCEROLYSIS; HIGH REACTION TEMPERATURES; HIGH SURFACE AREA; HOMOGENEOUS PROCESS; METHYL OLEATE; MOLAR RATIO; MONOGLYCERIDES; REACTION CONDITIONS; REACTION PARAMETERS; STIRRING RATES; UNSATURATED FATTY ACIDS;

EID: 72449167033     PISSN: 08885885     EISSN: None     Source Type: Journal    
DOI: 10.1021/ie9004783     Document Type: Article
Times cited : (37)

References (24)
  • 1
    • 34447129755 scopus 로고    scopus 로고
    • Chemical routes for the transformation of biomass into chemicals
    • Corma, A.; Iborra, S.; Velty, A. Chemical routes for the transformation of biomass into chemicals. Chem. Rev. 2007, 107, 2411-2502.
    • (2007) Chem. Rev. , vol.107 , pp. 2411-2502
    • Corma, A.1    Iborra, S.2    Velty, A.3
  • 2
    • 0842309061 scopus 로고    scopus 로고
    • Aqueous-phase reforming of oxygenated hydrocarbons over Sn-modified Ni catalysts
    • Shabaker, J. W.; Huber, G. W.; Dumesic, J. A. Aqueous-phase reforming of oxygenated hydrocarbons over Sn-modified Ni catalysts. J. Catal. 2004, 222, 180-191.
    • (2004) J. Catal. , vol.222 , pp. 180-191
    • Shabaker, J.W.1    Huber, G.W.2    Dumesic, J.A.3
  • 3
    • 33947706728 scopus 로고    scopus 로고
    • Processing biomass-derived oxygenates in the oil refinery: Catalytic cracking (FCC) reaction pathways and role of catalyst
    • Corma, A.; Huber, G. W.; Sauvanaud, L.; O'Connor, P. Processing biomass-derived oxygenates in the oil refinery: Catalytic cracking (FCC) reaction pathways and role of catalyst. J. Catal. 2007, 247, 307-327.
    • (2007) J. Catal. , vol.247 , pp. 307-327
    • Corma, A.1    Huber, G.W.2    Sauvanaud, L.3    O'Connor, P.4
  • 5
    • 61949418970 scopus 로고    scopus 로고
    • Commodity chemicals derived from glycerol, an important biorefinery feedstock
    • Zheng, Y.; Chen, X.; Shen, Y. Commodity chemicals derived from glycerol, an important biorefinery feedstock. Chem. Rev. 2008, 108, 5253-5277.
    • (2008) Chem. Rev. , vol.108 , pp. 5253-5277
    • Zheng, Y.1    Chen, X.2    Shen, Y.3
  • 6
    • 23944487842 scopus 로고    scopus 로고
    • Lewis and Brønsted basic active sites on solid catalysts and their role in the synthesis of monoglycerides
    • Corma, A.; Hamid, S. B. A.; Iborra, S.; Velty, A. Lewis and Brønsted basic active sites on solid catalysts and their role in the synthesis of monoglycerides. J. Catal. 2005, 234, 340-347.
    • (2005) J. Catal. , vol.234 , pp. 340-347
    • Corma, A.1    Hamid, S.B.A.2    Iborra, S.3    Velty, A.4
  • 7
    • 0020191326 scopus 로고
    • Glycerolysis of fats and methyl esters. Status, review, and critique
    • Sonntag, N. O. V. Glycerolysis of fats and methyl esters. Status, review, and critique. J. Am. Oil Chem. Soc. 1982, 59 (10), 795A-802A.
    • (1982) J. Am. Oil Chem. Soc. , vol.59 , Issue.10
    • Sonntag, N.O.V.1
  • 8
    • 0035949855 scopus 로고    scopus 로고
    • Glycerol transesterification with methyl stearate over solid basic catalysts I. Relationship between activity and basicity
    • Bancquart, S.; Vanhove, C.; Pouilloux, Y.; Barrault, J. Glycerol transesterification with methyl stearate over solid basic catalysts I. Relationship between activity and basicity. Appl. Catal. A: Gen. 2001, 218, 1-11.
    • (2001) Appl. Catal. A: Gen. , vol.218 , pp. 1-11
    • Bancquart, S.1    Vanhove, C.2    Pouilloux, Y.3    Barrault, J.4
  • 9
    • 3042735456 scopus 로고    scopus 로고
    • Selective glycerol transesterification over mesoporous basic catalysts
    • Barrault, J.; Bancquart, S.; Pouilloux, Y. Selective glycerol transesterification over mesoporous basic catalysts. C.R. Chim. 2004, 767, 593-599.
    • (2004) C.R. Chim. , vol.767 , pp. 593-599
    • Barrault, J.1    Bancquart, S.2    Pouilloux, Y.3
  • 10
    • 33646188709 scopus 로고    scopus 로고
    • Aldol condensation of citral with acetone on MgO and alkali-promoted MgO catalysts
    • Díez, V. K.; Apesteguía, C. R.; Di Cosimo, J. I. Aldol condensation of citral with acetone on MgO and alkali-promoted MgO catalysts. J. Catal. 2006, 240, 235-244.
    • (2006) J. Catal. , vol.240 , pp. 235-244
    • Díez, V.K.1    Apesteguía, C.R.2    Di Cosimo, J.I.3
  • 11
    • 18144418156 scopus 로고    scopus 로고
    • Allylic alcohol synthesis by gas-phase hydrogen transfer reduction of unsaturated ketones
    • Di Cosimo, J. I.; Acosta, A.; Apesteguía, C. R. Allylic alcohol synthesis by gas-phase hydrogen transfer reduction of unsaturated ketones. J. Mol. Catal. A: Chem. 2005, 234, 111-120.
    • (2005) J. Mol. Catal. A: Chem. , vol.234 , pp. 111-120
    • Di Cosimo, J.I.1    Acosta, A.2    Apesteguía, C.R.3
  • 12
    • 0342995808 scopus 로고    scopus 로고
    • Acid-base properties and active site requirements for elimination reactions on alkali-promoted MgO catalysts
    • Díez, V. K.; Apesteguía, C. R.; Di Cosimo, J. I. Acid-base properties and active site requirements for elimination reactions on alkali-promoted MgO catalysts. Catal. Today 2000, 63, 53-62.
    • (2000) Catal. Today , vol.63 , pp. 53-62
    • Díez, V.K.1    Apesteguía, C.R.2    Di Cosimo, J.I.3
  • 13
    • 0000941774 scopus 로고    scopus 로고
    • Base catalysis for the synthesis of α β,-unsaturated ketones from the vapor-phase aldol condensation of acetone
    • Di Cosimo, J. I.; Díez, V. K.; Apesteguía, C. R. Base catalysis for the synthesis of α β,-unsaturated ketones from the vapor-phase aldol condensation of acetone. Appl. Catal. A: Gen. 1996, 13, 149-166.
    • (1996) Appl. Catal. A: Gen. , vol.13 , pp. 149-166
    • Di Cosimo, J.I.1    Díez, V.K.2    Apesteguía, C.R.3
  • 15
    • 0014242337 scopus 로고
    • Bis (trimethylsilyl) acetamide in the silylation of lipolysis products for gas-liquid chromatography
    • Tallent, W. H.; Kleiman, R. Bis (trimethylsilyl) acetamide in the silylation of lipolysis products for gas-liquid chromatography. J. Lipid Res. 1968, 9, 146-148.
    • (1968) J. Lipid Res. , vol.9 , pp. 146-148
    • Tallent, W.H.1    Kleiman, R.2
  • 18
    • 33744543150 scopus 로고    scopus 로고
    • Liquid-liquid phase equilibrium in glycerol-methanol-methyl oleate and glycerol-monoolein-methyl oleate ternary systems
    • Negi, D. S.; Sobotka, F.; Kimmel, T.; Wozny, G.; Schomaecker, R. Liquid-liquid phase equilibrium in glycerol-methanol-methyl oleate and glycerol-monoolein-methyl oleate ternary systems. Ind. Eng. Chem. Res. 2006, 45, 3693-3696.
    • (2006) Ind. Eng. Chem. Res. , vol.45 , pp. 3693-3696
    • Negi, D.S.1    Sobotka, F.2    Kimmel, T.3    Wozny, G.4    Schomaecker, R.5
  • 19
    • 33747333104 scopus 로고    scopus 로고
    • Simulation of heterogeneously MgO-catalyzed transesterification for finechemical and biodiesel industrial production
    • Dossin, T. F.; Reyniers, M. F.; Berger, R. J.; Marin, G. B. Simulation of heterogeneously MgO-catalyzed transesterification for finechemical and biodiesel industrial production. App. Catal. B: Environ. 2006, 67, 136-148.
    • (2006) App. Catal. B: Environ. , vol.67 , pp. 136-148
    • Dossin, T.F.1    Reyniers, M.F.2    Berger, R.J.3    Marin, G.B.4
  • 21
    • 0020205049 scopus 로고
    • Experimental criterion for the absence of artifacts in the measurement of rates of heterogeneous catalytic reactions
    • Madon, R. J.; Boudart, M. Experimental criterion for the absence of artifacts in the measurement of rates of heterogeneous catalytic reactions. Ind. Eng. Chem. Fundam. 1982, 21, 438-447.
    • (1982) Ind. Eng. Chem. Fundam. , vol.21 , pp. 438-447
    • Madon, R.J.1    Boudart, M.2


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