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Volumn 1, Issue 8, 2013, Pages 974-981

Sustainable recycling of benzoic acid production waste: Green and highly efficient methods to separate and recover high value-added conjugated aromatic compounds from industrial residues

Author keywords

6H Benzo c chromen 6 one; 9 Fluorenone; Benzoic acid industrial residue; Biphenyl carboxylic acids; Sustainable chemistry

Indexed keywords

6H-BENZO[C]CHROMEN-6-ONE; 9-FLUORENONE; ECONOMIC EFFECTIVENESS; ENVIRONMENTAL CONTAMINATION; ENVIRONMENTAL POLLUTIONS; INDUSTRIAL PRODUCTION; INDUSTRIAL RESIDUES; SUSTAINABLE CHEMISTRY;

EID: 84881402799     PISSN: None     EISSN: 21680485     Source Type: Journal    
DOI: 10.1021/sc400059j     Document Type: Article
Times cited : (7)

References (35)
  • 1
  • 2
    • 67649622839 scopus 로고    scopus 로고
    • Sustainable chemical manufacturing: A matter of resources, wastes, hazards, and costs
    • Lange, J.-P. Sustainable chemical manufacturing: A matter of resources, wastes, hazards, and costs ChemSusChem 2009, 2 (6) 587-592
    • (2009) ChemSusChem , vol.2 , Issue.6 , pp. 587-592
    • Lange, J.-P.1
  • 3
    • 0025718984 scopus 로고
    • Effect of benzoic acid on glycolytic metabolite levels and intracellular pH in Saccharomyces cerevisiae
    • Warth, A. D. Effect of benzoic acid on glycolytic metabolite levels and intracellular pH in Saccharomyces cerevisiae Appl. Environ. Microbiol. 1991, 57 (12) 3415-3417
    • (1991) Appl. Environ. Microbiol. , vol.57 , Issue.12 , pp. 3415-3417
    • Warth, A.D.1
  • 4
    • 84856597115 scopus 로고    scopus 로고
    • Assessment of antioxidant potentials of free and bound phenolics of Hemidesmus indicus (L) R.Br against oxidative damage
    • Jayaram, S.; Dharmesh, S. M. Assessment of antioxidant potentials of free and bound phenolics of Hemidesmus indicus (L) R.Br against oxidative damage Pharmacognosy Res. 2011, 3 (4) 225-231
    • (2011) Pharmacognosy Res. , vol.3 , Issue.4 , pp. 225-231
    • Jayaram, S.1    Dharmesh, S.M.2
  • 5
    • 74249100853 scopus 로고    scopus 로고
    • The synthesis, characterization and optical properties of novel, substituted, pyrazoly 1,3,4-oxadiazole derivatives
    • Lv, H.-S.; Zhao, B.-X.; Li, J.-K.; Xia, Y.; Lian, S.; Liu, W.-Y.; Gong, Z.-L. The synthesis, characterization and optical properties of novel, substituted, pyrazoly 1,3,4-oxadiazole derivatives Dyes Pigm. 2010, 86 (1) 25-31
    • (2010) Dyes Pigm. , vol.86 , Issue.1 , pp. 25-31
    • Lv, H.-S.1    Zhao, B.-X.2    Li, J.-K.3    Xia, Y.4    Lian, S.5    Liu, W.-Y.6    Gong, Z.-L.7
  • 6
    • 77956172742 scopus 로고    scopus 로고
    • Cytotoxicity of monomers, plasticizer and degradation by-products released from dental hard chairside reline resins
    • Chaves, C. A.; Machado, A. L.; Carlos, I. Z.; Giampaolo, E. T.; Pavarina, A. C.; Vergani, C. E. Cytotoxicity of monomers, plasticizer and degradation by-products released from dental hard chairside reline resins Dent. Mater. 2010, 26 (10) 1017-1023
    • (2010) Dent. Mater. , vol.26 , Issue.10 , pp. 1017-1023
    • Chaves, C.A.1    MacHado, A.L.2    Carlos, I.Z.3    Giampaolo, E.T.4    Pavarina, A.C.5    Vergani, C.E.6
  • 7
    • 84857548828 scopus 로고    scopus 로고
    • Interfacial modification of organic photovoltaic devices by molecular self-organization
    • Tada, A.; Geng, Y.-F.; Nakamura, M.; Wei, Q.-S.; Hashimoto, K.; Tajima, K. Interfacial modification of organic photovoltaic devices by molecular self-organization Phys. Chem. Chem. Phys. 2012, 14 (11) 3713-3724
    • (2012) Phys. Chem. Chem. Phys. , vol.14 , Issue.11 , pp. 3713-3724
    • Tada, A.1    Geng, Y.-F.2    Nakamura, M.3    Wei, Q.-S.4    Hashimoto, K.5    Tajima, K.6
  • 8
    • 77956444192 scopus 로고    scopus 로고
    • A direct, biomass-based synthesis of benzoic acid: Formic acid-mediated deoxygenation of the glucose-derived materials quinic acid and shikimic acid
    • Arceo, E.; Ellman, J. A.; Bergman, R. G. A direct, biomass-based synthesis of benzoic acid: Formic acid-mediated deoxygenation of the glucose-derived materials quinic acid and shikimic acid ChemSusChem 2010, 3 (7) 811-813
    • (2010) ChemSusChem , vol.3 , Issue.7 , pp. 811-813
    • Arceo, E.1    Ellman, J.A.2    Bergman, R.G.3
  • 10
    • 0038487135 scopus 로고    scopus 로고
    • 2: Effects of fluorinated surfactants
    • 2: Effects of fluorinated surfactants Catal. Today 2003, 81 (4) 673-679
    • (2003) Catal. Today , vol.81 , Issue.4 , pp. 673-679
    • Zhu, J.1    Tsang, S.C.2
  • 11
    • 14544293246 scopus 로고    scopus 로고
    • Selective liquid phase oxidation of toluene with air
    • Guo, C.-C.; Liu, Q.; Wang, X.-T.; Hu, H.-Y. Selective liquid phase oxidation of toluene with air Appl. Catal., A 2005, 282 (1-2) 55-59
    • (2005) Appl. Catal., A , vol.282 , Issue.12 , pp. 55-59
    • Guo, C.-C.1    Liu, Q.2    Wang, X.-T.3    Hu, H.-Y.4
  • 14
    • 71849103684 scopus 로고    scopus 로고
    • Development on the technique of total recovery of benzoic acid residue
    • Xu, J.; He, J.; Zhang, W.-J.; Yang, T.; Jiao, S.-J.; Hu, X.-D. Development on the technique of total recovery of benzoic acid residue Chin. J. Chem. Eng. 2009, 17 (4) 608-612
    • (2009) Chin. J. Chem. Eng. , vol.17 , Issue.4 , pp. 608-612
    • Xu, J.1    He, J.2    Zhang, W.-J.3    Yang, T.4    Jiao, S.-J.5    Hu, X.-D.6
  • 16
    • 35748977089 scopus 로고    scopus 로고
    • Internal structure visualization and lithographic use of periodic toroidal holes in liquid crystals
    • Yoon, D. K.; Choi, M. C.; Kim, Y. H.; Kim, M. W.; Lavrentovich, O. D.; Jung, H.-T. Internal structure visualization and lithographic use of periodic toroidal holes in liquid crystals Nat. Mater. 2007, 6, 866-870
    • (2007) Nat. Mater. , vol.6 , pp. 866-870
    • Yoon, D.K.1    Choi, M.C.2    Kim, Y.H.3    Kim, M.W.4    Lavrentovich, O.D.5    Jung, H.-T.6
  • 17
    • 67650689052 scopus 로고    scopus 로고
    • The synthesis and two-photon excited fluorescence properties of novel branched fluorene derivatives
    • Cao, D.; Liu, Z.; Deng, Y.; Li, G.; Zhang, G. The synthesis and two-photon excited fluorescence properties of novel branched fluorene derivatives Dyes Pigm. 2009, 83 (3) 348-353
    • (2009) Dyes Pigm. , vol.83 , Issue.3 , pp. 348-353
    • Cao, D.1    Liu, Z.2    Deng, Y.3    Li, G.4    Zhang, G.5
  • 18
    • 0020112895 scopus 로고
    • Liquid-chromatographic determination of rate constants for the cellulose-dimethyloldihydroxyethyleneurea reaction
    • Chen, C.-S.; Bulkin, B. J. Liquid-chromatographic determination of rate constants for the cellulose-dimethyloldihydroxyethyleneurea reaction J. Appl. Polym. Sci. 1982, 27 (4) 1177-1190
    • (1982) J. Appl. Polym. Sci. , vol.27 , Issue.4 , pp. 1177-1190
    • Chen, C.-S.1    Bulkin, B.J.2
  • 19
    • 73249138888 scopus 로고    scopus 로고
    • Synthesis of conjugated polymers for organic solar cell applications
    • Cheng, Y.-J.; Yang, S.-H.; Hsu, C.-S. Synthesis of conjugated polymers for organic solar cell applications Chem. Rev. 2009, 109 (11) 5868-5923
    • (2009) Chem. Rev. , vol.109 , Issue.11 , pp. 5868-5923
    • Cheng, Y.-J.1    Yang, S.-H.2    Hsu, C.-S.3
  • 20
    • 0032873205 scopus 로고    scopus 로고
    • Recent development in the design of organic materials for optical power limiting
    • Spangler, C. W. Recent development in the design of organic materials for optical power limiting J. Mater. Chem 1999, 9 (9) 2013-2020
    • (1999) J. Mater. Chem , vol.9 , Issue.9 , pp. 2013-2020
    • Spangler, C.W.1
  • 21
    • 77955365297 scopus 로고    scopus 로고
    • Electrochemical behavior and electrogenerated chemiluminescence of star-shaped D-A compounds with a 1,3,5-triazine core and substituted fluorene arms
    • Omer, K. M.; Ku, S.-Y.; Chen, Y.-C.; Wong, K.-T.; Bard, A. J. Electrochemical behavior and electrogenerated chemiluminescence of star-shaped D-A compounds with a 1,3,5-triazine core and substituted fluorene arms J. Am. Chem. Soc. 2010, 132 (31) 10944-10952
    • (2010) J. Am. Chem. Soc. , vol.132 , Issue.31 , pp. 10944-10952
    • Omer, K.M.1    Ku, S.-Y.2    Chen, Y.-C.3    Wong, K.-T.4    Bard, A.J.5
  • 22
    • 70349895550 scopus 로고    scopus 로고
    • An improved, highly efficient and green synthesis of bromofluorenones and nitrofluorenones in water
    • Zhang, X.; Han, J.-B.; Li, P.-F.; Ji, X.; Zhang, Z. An improved, highly efficient and green synthesis of bromofluorenones and nitrofluorenones in water Synth. Commun. 2009, 39 (21) 3804-3815
    • (2009) Synth. Commun. , vol.39 , Issue.21 , pp. 3804-3815
    • Zhang, X.1    Han, J.-B.2    Li, P.-F.3    Ji, X.4    Zhang, Z.5
  • 23
    • 17144405607 scopus 로고    scopus 로고
    • Dendrimer-encapsulated Pd nanoparticles as aqueous, room-temperature catalysts for the Stille reaction
    • Garcia-Martinez, J. C.; Lezutekong, R.; Crooks, R. M. Dendrimer-encapsulated Pd nanoparticles as aqueous, room-temperature catalysts for the Stille reaction J. Am. Chem. Soc. 2005, 127 (14) 5097-5103
    • (2005) J. Am. Chem. Soc. , vol.127 , Issue.14 , pp. 5097-5103
    • Garcia-Martinez, J.C.1    Lezutekong, R.2    Crooks, R.M.3
  • 24
    • 84866596662 scopus 로고    scopus 로고
    • Embossing of organic thin films using a surfactant assisted lift-off technique
    • Zhang, X.; Zhang, G.-X.; Liao, Y.-C.; Weeks, B. L. Embossing of organic thin films using a surfactant assisted lift-off technique J. Colloid Interface Sci. 2012, 387 (1) 175-179
    • (2012) J. Colloid Interface Sci. , vol.387 , Issue.1 , pp. 175-179
    • Zhang, X.1    Zhang, G.-X.2    Liao, Y.-C.3    Weeks, B.L.4
  • 25
    • 0032123374 scopus 로고    scopus 로고
    • Multistage separation of quinoline and iso-quinoline by dissociation extraction
    • Awar, M. M.; Arif, A. S.; Pritchard, D. W. Multistage separation of quinoline and iso-quinoline by dissociation extraction Solvent Extr. Ion Exch. 1998, 16 (4) 931-950
    • (1998) Solvent Extr. Ion Exch. , vol.16 , Issue.4 , pp. 931-950
    • Awar, M.M.1    Arif, A.S.2    Pritchard, D.W.3
  • 26
    • 78149428191 scopus 로고    scopus 로고
    • A novel microporous MOF with the capability of selective adsorption of xylenes
    • Jin, Z.; Zhao, H.-Y.; Zhao, X.-J.; Fang, Q.-R.; Long, J.-R.; Zhu, G.-S. A novel microporous MOF with the capability of selective adsorption of xylenes Chem. Commun. 2010, 46 (45) 8612-8614
    • (2010) Chem. Commun. , vol.46 , Issue.45 , pp. 8612-8614
    • Jin, Z.1    Zhao, H.-Y.2    Zhao, X.-J.3    Fang, Q.-R.4    Long, J.-R.5    Zhu, G.-S.6
  • 27
    • 77952577397 scopus 로고    scopus 로고
    • Adsorption and separation of reactive aromatic isomers and generation and stabilization of their radicals within cadmium(II)-triazole metal-organic confined space in a single-crystal-to-single-crystal fashion
    • Liu, Q.-K.; Ma, J.-P.; Don, Y.-B. Adsorption and separation of reactive aromatic isomers and generation and stabilization of their radicals within cadmium(II)-triazole metal-organic confined space in a single-crystal-to-single- crystal fashion J. Am. Chem. Soc. 2010, 132 (20) 7005-7017
    • (2010) J. Am. Chem. Soc. , vol.132 , Issue.20 , pp. 7005-7017
    • Liu, Q.-K.1    Ma, J.-P.2    Don, Y.-B.3
  • 28
    • 0344898485 scopus 로고    scopus 로고
    • Direct separation and quantitative determination of glimepiride isomers by high performance liquid chromatography
    • Song, Y.-R.; Niu, L.-P.; Wang, D.-F.; Hu, Y.-P.; Hou, D.-Y. Direct separation and quantitative determination of glimepiride isomers by high performance liquid chromatography J. Sep. Sci. 2003, 26 (17) 1595-1597
    • (2003) J. Sep. Sci. , vol.26 , Issue.17 , pp. 1595-1597
    • Song, Y.-R.1    Niu, L.-P.2    Wang, D.-F.3    Hu, Y.-P.4    Hou, D.-Y.5
  • 29
    • 37049148636 scopus 로고
    • The separation of β-picoline, γ-picoline, and 2:6-lutidine from their mixture
    • Lidstone, A. G. The separation of β-picoline, γ-picoline, and 2:6-lutidine from their mixture J. Chem. Soc. 1940, 1, 241-243
    • (1940) J. Chem. Soc. , vol.1 , pp. 241-243
    • Lidstone, A.G.1
  • 30
    • 0042178955 scopus 로고
    • Separation of conformers. II. Axial and equatorial isomers of chlorocyclohexane and trideuteriomethoxycyclohexane
    • Jensen, F. R.; Bushweller, C. H. Separation of conformers. II. Axial and equatorial isomers of chlorocyclohexane and trideuteriomethoxycyclohexane J. Am. Chem. Soc. 1969, 91 (12) 3223-3225
    • (1969) J. Am. Chem. Soc. , vol.91 , Issue.12 , pp. 3223-3225
    • Jensen, F.R.1    Bushweller, C.H.2
  • 32
    • 79960245352 scopus 로고    scopus 로고
    • Highly efficient synthesis of 9-fluorenones from 9H-fluorenes by air oxidation
    • Zhang, X.; Ji, X.; Jiang, S.-S.; Liu, L.-L.; Weeks, B. L.; Zhang, Z. Highly efficient synthesis of 9-fluorenones from 9H-fluorenes by air oxidation Green Chem. 2011, 13 (7) 1891-1896
    • (2011) Green Chem. , vol.13 , Issue.7 , pp. 1891-1896
    • Zhang, X.1    Ji, X.2    Jiang, S.-S.3    Liu, L.-L.4    Weeks, B.L.5    Zhang, Z.6
  • 33
    • 79953057407 scopus 로고    scopus 로고
    • Highly efficient amine-based catalytic system for room temperature Suzuki-Miyaura reactions of aryl halides with arylboronic acids
    • Das, P.; Sarmah, C.; Tairai, A.; Bora, U. Highly efficient amine-based catalytic system for room temperature Suzuki-Miyaura reactions of aryl halides with arylboronic acids Appl. Organometal. Chem. 2011, 2 (4) 283-288
    • (2011) Appl. Organometal. Chem. , vol.2 , Issue.4 , pp. 283-288
    • Das, P.1    Sarmah, C.2    Tairai, A.3    Bora, U.4
  • 34
    • 80052099052 scopus 로고    scopus 로고
    • tBu promoted intramolecular cross coupling to approach fused rings
    • tBu promoted intramolecular cross coupling to approach fused rings Chem. Commun. 2011, 47 (35) 9813-9815
    • (2011) Chem. Commun. , vol.47 , Issue.35 , pp. 9813-9815
    • Sun, C.-L.1    Gu, Y.-F.2    Huang, W.-P.3    Shi, Z.-J.4
  • 35
    • 25844440760 scopus 로고    scopus 로고
    • General catalysts for the Suzuki-Miyaura and Sonogashira coupling reactions of aryl chlorides and for the coupling of challenging substrate combinations in water
    • Anderson, K. W.; Buchwald, S. L. General catalysts for the Suzuki-Miyaura and Sonogashira coupling reactions of aryl chlorides and for the coupling of challenging substrate combinations in water Angew. Chem., Int. Ed. 2005, 44 (38) 6173-6177
    • (2005) Angew. Chem., Int. Ed. , vol.44 , Issue.38 , pp. 6173-6177
    • Anderson, K.W.1    Buchwald, S.L.2


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