Fabrication and characterization of perovskite-type oxide LaFe0.9Co0.1O3 nanoparticles and its performance in aerobic oxidation of thiols to disulfide

Cuihua Xuebao/Chinese Journal of Catalysis

Volumn 33, Issue 11, 2012, Pages 1791-1796

  Tabari, Taymaz ^a   Tavakkoli, Haman ^b  

^a ISLAMIC AZAD UNIVERSITY   (Iran)

^b ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

Nanopowder; Oxidation of thiols; Perovskite type oxide; Sol gel method

Indexed keywords

AEROBIC OXIDATIONS; ALIPHATIC THIOLS; CRYSTALLINE PHASE; ENERGY DISPERSIVE X RAY SPECTROSCOPY; HIGHER YIELD; NANO POWDERS; OXIDATION REACTIONS; PEROVSKITE TYPE OXIDES; PHYSICAL AND CHEMICAL PROPERTIES; REACTION PARAMETERS; TRANSMISSION ELECTRON; XRD;

CATALYSTS; CHEMICAL PROPERTIES; FOURIER TRANSFORM INFRARED SPECTROSCOPY; LANTHANUM ALLOYS; NANOPARTICLES; PEROVSKITE; SCANNING ELECTRON MICROSCOPY; SCANNING TUNNELING MICROSCOPY; SOL-GEL PROCESS; THERMOGRAVIMETRIC ANALYSIS; TRANSMISSION ELECTRON MICROSCOPY; X RAY DIFFRACTION; X RAY SPECTROSCOPY;

OXIDATION;

EID: 84871827367     PISSN: 02539837     EISSN: None     Source Type: Journal    
DOI: 10.1016/s1872-2067(11)60442-7     Document Type: Article

References (28)

1. Moser W R. Catalytic Chemistry of Solid State Inorganics. New York: New York Academy of Sciences, 1976
2. Centi G, Trifiro F. Catal Rev Sci Eng, 1986, 28: 165
3. Mizuno N, Misono M. Chem Rev, 1998, 98: 199
4. Pena M A, Fierro J L G. Chem Rev, 2001, 101: 1981
5. Leion H, Larring Y, Bakken E, Bredesen R, Mattisson T, Lyngfelt A. Energy Fuels, 2009, 23: 5276
6. Ryden M, Lyngfelt A, Mattisson T, Chen D, Holmen A, Bjorgum E. Int J Green Gas Con, 2008, 2: 21
7. Hossain M M, de Lasa H I. Chem Eng Sci, 2008, 63: 4433
8. Evdou A, Zaspalis V, Nalbandian L. Fuel, 2010, 89: 1265
9. Nalbandian L, Evdou A, Zaspalis V. Int J Hydrogen Energy, 2009, 34: 7162
10. Jocelyn D C. Biochemistry of the Thiol Group. New York: Academic Press, 1992
11. Firouzbadi H, Iranpoor N, Parham H A, Sardarian A, Toofan J. Synth Commun, 1984, 14: 717
12. Wallace T J. J Org Chem, 1966, 31: 1217
13. Liu K T, Tong Y C. Synthesis, 1978: 669
14. Pryor W A, Church D F, Govindan C K, Crank G. J Org Chem, 1982, 47: 156
15. Ali M H, McDermott M. Tetrahedron Lett, 2002, 43: 6271
16. McKillop A, Koyuncu D, Krief A, Dumont W, Renier P, Trabelsi M. Tetrahedron Lett, 1990, 31: 5007
17. Evans B J, Doi J T, Musker W K. J Org Chem, 1990, 55: 2337
18. Shaabani A, Lee D G. Tetrahedron Lett, 2001, 42: 5833
19. Tajbakhsh M, Hosseinzadeh R, Shakoori A. Tetrahedron Lett, 2004, 45: 1889
20. Khazaei A, Zolfigol M A, Rostami A. Synthesis, 2004: 2959
21. Akdag A, Webb T, Worley S D. Tetrahedron Lett, 2006, 47: 3509
22. Shaabani A, Teimouri F, Lee D G. Synth Commun, 2003, 33: 1057
23. Ordonez S, Paredes J R, Dìez F V. Appl Catal A, 2008, 341: 174
24. Campagnoli E, Tavares A, Fabbrini L, Rossetti I, Pubitsky Y A, Zaopo A, Forni L. Appl Catal B, 2005, 55: 133
25. Yazdanbakhsh M, Tavakkoli H, Hosseini S M. Desalination, 2010, 281: 388
26. Vogel A I. A Text Book of Practical Organic Chemistry. London: Longman Green, 1959
27. Shaabani A, Safari N, Shoghpour S, Rezayan A H. Monatsh Chem, 2008, 139: 613
28. Eshtiagh-Hosseini H, Housaindokht M R, Shoghpour S. React Kinet Catal Lett, 2010, 100: 105