A non-chromatographic method for the separation of highly pure naphthalene crystals from pyrolysis fuel oil

Separation and Purification Technology

Volumn 80, Issue 1, 2011, Pages 90-95

  Mayani, Vishal J ^a   Mayani, Suranjana V ^a   Lee, Yonghwa ^b   Park, Seung Kyu ^b  

^a Dongguk University   (South Korea)

^b Hoseo University   (South Korea)

Author keywords

Naphthalene crystals; Pyrolysis fuel oil (PFO); Self crystallization; Solvent extraction

Indexed keywords

ANALYTICAL TECHNIQUES; COOLING PROCESS; INNOVATIVE APPROACHES; SELF-CRYSTALLIZATION; SOLVENT EXTRACTION METHODS;

CHROMATOGRAPHIC ANALYSIS; CHROMATOGRAPHY; CRYSTALLIZATION; ETHANOL; FUEL OILS; FUELS; ORGANIC SOLVENTS; PYROLYSIS; SOLVENT EXTRACTION; SOLVENTS;

NAPHTHALENE;

EID: 79959689370     PISSN: 13835866     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.seppur.2011.04.013     Document Type: Article

References (29)

1. M.S. Smyth, I. Stefanova, I.D. Horak Jr., and T.R. Burke Hydroxylated 2-(5'-salicyl) naphthalenes as protein-tyrosine kinase inhibitors J. Med. Chem. 36 1993 3015 3020 (Pubitemid 23315407)
2. H. Zhao, N. Neamati, A. Mazumder, S. Sunder, Y. Pommier Jr., and T.R. Burke Arylamide inhibitors of HIV-1 integrase J. Med. Chem. 40 1997 1186 1194 (Pubitemid 27175097)
3. T. Ukita, Y. Nakamura, A. Kubo, Y. Yamamoto, M. Takahashi, J. Kotera, and T. Ikeo 1-Arylnaphthalene lignan: a novel scaffold for type 5 phosphodiesterase inhibitor J. Med. Chem. 42 1999 1293 1305 (Pubitemid 29181151)
4. S. Asir, A.S. Demir, and H. Icil The synthesis of novel, unsymmetrically substituted, chiral naphthalene and perylene diimides: photophysical, electrochemical, chiroptical and intramolecular charge transfer properties Dyes Pigm. 84 2010 1 13
5. J.L. Charlton, C.J. Oleschuk, and G.L. Chee Hindered rotation in arylnaphthalene lignans J. Org. Chem. 61 1996 3452 3457 (Pubitemid 126575794)
6. P.S. Karnik, S. Kulkarni, X.P. Liu, G.T. Budd, and R.M. Bukowski Estrogen receptor mutations in tamoxifen-resistant breast cancer Cancer Res. 54 1994 349 353 (Pubitemid 24053165)
7. J. Fang, A. Akwabi-Ameyaw, J.E. Britton, S.R. Katamreddy, F. Navas, A.B. Miller, S.P. Williams, D.W. Gray, L.A. Orband-Miller, J. Shearin, and D. Heyer Synthesis of 3-alkyl naphthalenes as novel estrogen receptor ligands Bioorg. Med. Chem. Lett. 18 2008 5075 5077
8. T. Charinpanitkul, N. Sano, P. Puengjinda, J. Klanwan, N. Akrapattangkul, and W. Tanthapanichakoon Naphthalene as an alternative carbon source for pyrolytic synthesis of carbon nanostructures J. Anal. Appl. Pyrolysis 86 2009 386 390
9. 3 Carbon 36 1998 369 375 (Pubitemid 128400411)
10. M. Dumont, G. Chollon, M.A. Dourges, R. Pailler, X. Bourrat, R. Naslain, J.L. Bruneel, and M. Couzi Chemical, microstructural and thermal analyses of a naphthalene-derived mesophase pitch Carbon 40 2002 1475 1486 (Pubitemid 34623840)
11. C.L. Kao, S.Y. Yen, and J.W. Chern A new route towards the synthesis of substituted naphthalenes via Friedel-Crafts acylation Tetrahedron Lett. 41 2000 2207 2210 (Pubitemid 30183005)
12. A.R. Katritzky, G. Zhang, and L. Xie Benzotriazole-assisted aromatic ring annulation: efficient and general syntheses of polysubstituted naphthalenes and phenanthrenes J. Org. Chem. 62 1997 721 725 (Pubitemid 127493292)
13. C.B.d. Koning, J.P. Michael, and A.L. Rousseau A novel method for the synthesis of substituted naphthalenes and phenanthrenes J. Chem. Soc. Perkin Trans. 1 2000 787 797 (Pubitemid 35290467)
14. G. Collin, H. Höke, and H. Greim Naphthalene and hydronaphthalenes in Ullmann's encyclopedia of industrial chemistry 2003 Wiley-VCH Weinheim
15. P.E. Reichardt, and L.d. White Estimation of naphthalene in absorbing oil Ind. Eng. Chem. Anal. Ed. 18 1946 286 288
16. A.D. Sulimov, I.N. Kozhina, and D.M. Trakhtenberg The production of naphthalene from petroleum crude Chem. Tech. Fuels Oils 1 1965 20 24
17. S.R. Kang, J.Y. Koh, C.U. Kim, and S.J. Park Effect of cooling rate and crystallizer type on separation of naphthalene mixture by layer melt crystallization Clean Tech. 13 2007 72 78
18. S. Sporring, S. Bøwadt, B. Svensmark, and E. Bjorklund Comprehensive comparison of classic Soxhlet extraction with Soxtec extraction, ultrasonication extraction, supercritical fluid extraction, microwave assisted extraction and accelerated solvent extraction for the determination of polychlorinated biphenyls in soil J. Chromatogr. A 1090 2005 1 9 (Pubitemid 41207660)
19. Z.X. Liu, J.N. Park, S.H.R. Abdi, S.K. Park, Y.K. Park, and C.W. Lee Nano-sized carbon hollow spheres for abatement of ethylene Topics Catal. 39 2006 221 226
20. S.B. Yoon, J.Y. Kim, J.H. Kim, S.G. Park, J.Y. Kim, C.W. Lee, and J.S. Yu Template synthesis of nanostructured silica with hollow core and mesoporous shell structures Curr. Appl. Phy. 6 2006 1059 1063 (Pubitemid 44131672)
21. J.K. Lee, S.Y. Han, S.K. Park, Y.K. Park, and C.W. Lee Activation of nano-sized carbon shells on carbon hollow spheres under water vapor Korean J. Chem. Eng. 22 2005 42 45 (Pubitemid 40541414)
22. Y. Meng, D. Gu, F. Zhang, Y. Shi, H. Yang, Z. Li, C. Yu, B. Tu, and D. Zhao Ordered mesoporous polymers and homologous carbon frameworks: amphiphilic surfactant templating and direct transformation Angew. Chem. Int. Ed. 44 2005 7053 7059 (Pubitemid 41587571)
23. S.K. Park, S.B. Yoon, D. Zhao, Y. Meng, D. Gu, Y. Shi, Ordered mesoporous polymers and homologous carbon frameworks: amphiphilic surfactant templating and direct transformation, Korean Patent A 2007-0024435, 2007.
24. V.J. Mayani, S.H.R. Abdi, R.I. Kureshy, N.H. Khan, S. Agrawal, and R.V. Jasra Synthesis and characterization of (S)-amino alcohol modified M41S as effective material for the enantioseparation of racemic compounds J. Chromatogr. A 1135 2006 186 193 (Pubitemid 44692698)
25. V.J. Mayani, S.H.R. Abdi, R.I. Kureshy, N.H. Khan, S. Agrawal, and R.V. Jasra Synthesis and characterization of mesoporous silica modified with chiral auxiliaries for their potential application as chiral stationary phase J. Chromatogr. A 1191 2008 223 230
26. V.J. Mayani, S.H.R. Abdi, R.I. Kureshy, N.H. Khan, S. Agrawal, and R.V. Jasra Enantiomer self-disproportionation of chiral compounds on achiral ordered mesoporous silica M41S and regular silica gel as a stationary phase Chirality 21 2009 255 261
27. V.J. Mayani, S.H.R. Abdi, R.I. Kureshy, N.H. Khan, A. Das, and H.C. Bajaj Heterogeneous chiral copper complexes of amino alcohol for asymmetric nitroaldol reaction J. Org. Chem. 75 2010 6191 6195
28. S. Selvakumar, K. Sivaji, A. Arulchakkaravarthi, N. Balamurugan, S. Sankar, and P. Ramasamy Growth of high-quality naphthalene single crystals using selective self-seeding vertical Bridgman technique (SSVBT) and its characterization J. Crystal Growth 282 2005 370 375 (Pubitemid 41085130)
29. W. Li, Z. Liu, Z. Wang, L. Chen, Y. Sun, J. Hou, and Y. Zheng Application of accelerated solvent extraction to the investigation of saikosaponins from the roots of Bupleurum falcatum J. Sep. Sci. 33 2010 1870 1876