•  
  •  
 

Abstract

Cylohexane oxidation is of great industrial importance in the production of intermediates for the manufacture of nylon6 and nylon-6,6. Most cyclohexane is commercially converted into a cyclohexanone–cyclohexanol mixture (known as K-A oil) by catalytic oxidation. K-A (Ketone-Alcohol) oil is then used as a raw material for adipic acid and caprolactam production. Practically, if the cyclohexanol content of KA oil is higher than that of cyclohexanone, it is more profitable to convert it into adipic acid; otherwise caprolactam production is more likely. The steady state cyclohexane oxidation reaction model in a stirred tank reactor for K-A oil production is presented and solved in this paper. The model was derived based on the mass balance and mass transfer equations using the kinetic equation. The set of algebraic equations was solved using non linear programming. The advantage of this method is that the relationship among variables can be better understood and an appropriate solution to the equation set can be obtained more quickly. Simulation results are particularly useful for process design such as in determining reactor dimensions and operating conditions.

References

[1] J. Alagy, P. Trambouze, H.V. Landeghem, Ind. Eng. Chem. Process Des. Develop. 13/4 (1974) 317. [2] A.K. Suresh, T. Sridhar, O.E. Potter, AIChE J. 34 (1988) 69. [3] P. Liu, L. Zou, H. Luo, Chinese J. Chem. Eng. 12/1 (2004) 49. [4] V. Govindan, A.K. Suresh, Ind. Eng. Chem. Res. 46/21 (2007) 6891. [5] R. Pohorecki, J. Baldyga, W. Moniuk, W. Podgorska, A. Zdrojkowski, P.T. Wierzchowski, Chem. Eng. Sci. 56 (2001) 1285. [6] A. Bhattacharya, Chem. Eng. Process. 44 (2005) 567. [7] The Flixborough Disaster. Report of the Court Inquiry, Department of Employment, London, 1975, p.108. http://www.icheme.org/resources/safety_centre /publications/~/media/Documents/icheme/Safety% 20Centre/HSE%20reports/Flixborough.pdf. [8] G.B. Tatterson, Fluid Mixing and Gas Dispersion in Agitated Tanks, McGraw-Hill, New York, 1991, p.564. [9] M. Spielman, AIChE J. 10/4 (1964) 496. [10] D.G. Rao, R.S. Tirukkoyllur, Ind. Eng. Chem. Process. Des. Dev. 25 (1986) 299. [11] C. Shi, B. Zhu, M. Lin, J. Long, R. Wang, Catal. Today, 175/1 (2010) 398. [12] K.S. Anisia, A. Kumar, J. Mol. Catal. 271/1-2 (2007) 164. [13] W.A. Carvalho, P.B. Varaldo, M. Wallau, U. Schuchardt, Zeolites, 18 (1997) 408. [14] J. Hao, J. Wang, Q. Wang, Y. Yu, S. Cai, Appl. Catal. A: General, 368/1-2 (2009) 29. [15] B. Modén, B.-Z. Zhan, J. Dakka, J.G. Santiesteban, E. Iglesia, J. Catal. 239/2 (2006) 390. [16] J-Y. Wang, F.-Y. Zhao, R.-J. Liu, Y.-Q. Hu, J. Mol. Catal. A: Chem. 279/2 (2008) 153. [17] K.S. Anisia, A. Kumar, Appl. Catal. 273/1-2 (2004) 193.

Share

COinS
 
 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.