Liquid phase oxidation of p-xylene to terephthalic acid at medium-high temperatures: Multiple benefits of CO2-expanded liquids

Green Chemistry

Volumn 12, Issue 2, 2010, Pages 260-26

  Zuo, Xiaobin ^a   Niu, Fenghui ^a   Snavely, Kirk ^a,b   Subramaniam, Bala ^a,b   Busch, Daryle H ^a  

^a UNIVERSITY OF KANSAS   (United States)

^b University of Kansas   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 76349123627     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/b920262e     Document Type: Article

References (32)

1. W. Partenheimer Catal. Today 1995 23 69-158.
2. P. Raghavendrachar S. Ramachandran Ind. Eng. Chem. Res. 1992 31 453-462.
3. H. Milan, A. G. Hussain and R. Roberto, US Pat., 20080293964.
4. P. A. Hamley T. Ilkenhans J. M. Webster E. Garcia-Verdugo E. Vernardou M. J. Clarke R. Auerbach W. B. Thomas K. Whiston M. Poliakoff Green Chem. 2002 4 235-238.
5. J. B. Dunn P. E. Savage Environ. Sci. Technol. 2005 39 5427-5435.
6. Y. S. Chen J. L. Fulton W. Partenheimer J. Am. Chem. Soc. 2005 127 14085-14093.
7. P. Jessop B. Subramaniam Chem. Rev. 2006 107 2666-2694.
8. T. Seki A. Baiker Chem. Rev. 2009 109 2409-2454.
9. C. A. Eckert D. Bush J. S. Brown C. L. Liotta Ind. Eng. Chem. Res. 2000 39 4615-4621.
10. C. A. Eckert C. L. Liotta D. Bush J. S. Brown J. P. Hallett J. Phys. Chem. B 2004 108 18108-18118.
11. G. T. Musie M. Wei B. Subramaniam D. H. Busch Coord. Chem. Rev. 2001 219 789-820.
12. M. Wei G. T. Musie D. H. Busch B. Subramaniam J. Am. Chem. Soc. 2002 124 2513-2517.
13. M. Wei G. T. Musie D. H. Busch B. Subramaniam Green Chem. 2004 6 387-394.
14. X. Zuo B. Subramaniam D. H. Busch Ind. Eng. Chem. Res. 2008 47 546-552.
15. M. A. Zeitlin and D. Wilger-Nowicki, US Pat., 5 095 146, 1992.
16. H. Jin B. Subramaniam A. Ghosh J. Tunge AIChE J. 2006 52 2575-2581.
17. B. Rajagopalan M. Wei G. T. Musie B. Subramaniam D. H. Busch Ind. Eng. Chem. Res. 2003 42 6505-6510.
18. D. R. Burri K. W. Jun J. S. Yoo C. W. Lee S. E. Park Catal. Lett. 2002 81 169-173.
19. J. S. Yoo S. H. Jhung K. H. Lee Y. S. Park Appl. Catal. A-Gen. 2002 223 239-251.
20. S. E. Park J. S. Chang K. W. Lee Stud. Surf. Sci. Catal. 2004 153 303-314.
21. P. Roffia P. Calini L. Motta Ind. Eng. Chem. Prod. Res. Dev. 1984 23 629-634.
22. Personal Communication, BP Personnel (names provided in the acknowledgement section), 2007.
23. G. G. Lavoie, R. T. Hembre, C. E. J. Sumner, J. N. Bays, D. B. Compton, B. A. Tennant, B. W. Davenport, D. Lange and T. R. Floyd, PCT Int. Appl. 2006, WO 2006096312.
24. S. H. Jhung Y. S. Park Bull. Korean Chem. Soc. 2002 23 369-373.
25. A. W. Chester E. J. Y. Scott P. S. Landis J. Catal. 1977 46 308-319.
26. R. L. June, M. W. Potter, E. J. Simpson and C. L. Edwards, US Pat., 6 153 790, 2000.
27. W. Partenheimer J. Mol. Catal. A-Chem. 2003 206 105-119.
28. W. Partenheimer, US Pat., 4 992 580, 1991.
29. B. Rajagopalan, Ph.D. Thesis, University of Kansas, 2007.
30. W. Partenheimer, in Catalysis of Organic Reactions, ed. D. W. Blackburn, Marcel Dekker, New York, 1990, pp. 321-346.
31. P. D. Metelski and J. H. Espenson, PCT Int. Appl. 2005, WO 2005000779.
32. Y. Cheng L. Zhang G. Xie X. Li Chem. React. Eng. Technol. (China) 2003 19 182-187.