Cite

1. Cornils, B. & Lappe, P. (2010). Dicarboxylic Acids, Aliphatic. Ullmann’s Encyclopedia of Industrial Chemistry, Wiley- -VCH, Weinheim.10.1002/14356007.a08_523.pub2Search in Google Scholar

2. (2018, Febuary). Malic Acid Market Size, Share, Trend Analysis Report By End-use (Beverage, Confectionery, Personal Care & Cosmetics), By Region, Competitive Landscape, And Segment Forecasts, 2014-2024. Retrieved March 03, 2018, from https://www.grandviewresearch.com/industry-analysis/malic-acid-marketSearch in Google Scholar

3. (2015, November). Another biobased dicarboxylic acid moves toward commercial production, by Verdezyne. Retrieved March 03, 2018, from https://www.biobasedpress.eu/2015/11/another-biobased-dicarboxylic-acid-comes-into-commercialproduction-by-verdezyneSearch in Google Scholar

4. (2017, June). Adipic Acid. Chemical Economics Handbook. Retrieved March 03, 2018, from https://ihsmarkit.com/products/adipic-acid-chemical-economics-handbook.htmlSearch in Google Scholar

5. Krzysztoforski, A., Wojcik, Z., Pohorecki, R. & Baldyga, J. (1986). Industrial contribution to the reaction engineering of cyclohexane oxidation. Ind. Eng. Chem. Process Des. Dev. Industrial 25(4), 894-898. DOI: 10.1021/i200035a010.10.1021/i200035a010Open DOISearch in Google Scholar

6. Oczkowicz, S., Rygiel S., Wais, J., Koziol, A., Gruszka, M., Kondrat, A., Pohorecki, R., Wierzchowski, P., Moniuk, W., Krzysztoforski, A., Mijal, W., Wójcik, Z. & Zylinski, M. (2006). EP Patents No. 1,720,641. Paris, European Patent Office.Search in Google Scholar

7. Weissermel, K. & Arpe, H.J. (1997). Industrial Organic Chemistry (3 th ed.). New York, British Library CataloguingSearch in Google Scholar

8. Krzysztoforski, A. & Rygiel, S. (2016). Produkcja cykloheksanonu. Od fenolu do benzenu i z powrotem? Przem. Chem. 6(95), 1049-1248. DOI: 10.15199/62.2016.6.110.15199/62.2016.6.1Search in Google Scholar

9. (2015, September). Global Markets for Adipic Acid. Retrieved March 03, 2018, from http://www.researchandmarkets.com/reports/3641969/global-markets-for-adipic-acid#relc2Search in Google Scholar

10. Teles, J.H., Hermans, I., Franz, G. & Sheldon R.A. (2015). Oxidation. Ullmann’s Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim.10.1002/14356007.a18_261.pub2Search in Google Scholar

11. Lisicki, D., Dobras, G., Orlińska, B. & Zawadiak, J. (2017). Metody otrzymywania kwasu adypinowego o potencjalnym zastosowaniu przemysłowym. Przem. Chem. 96(7), 1485-1489. DOI: 10.15199/62.2017.7.7.10.15199/62.2017.7.7Search in Google Scholar

12. Cavani, F. & Teles, J.H. (2009). Sustainability in catalytic oxidation: An alternative approach or a structural evolution? Chem. Sus. Chem. 2(6), 508-534. DOI: 10.1002/cssc.200900020.10.1002/cssc.20090002019536755Open DOISearch in Google Scholar

13. (1998, December). One Step Phenol from Benzene by the AlphOx Process. Retrieved March 03, 2018, from https://ihsmarkit.com/products/chemical-technology-pep-reviews-onestep-phenol-from-benzene-1998.htmlSearch in Google Scholar

14. Notté, P.P. (2000). The AlphOx TM process or the onestep hydroxylation of benzene into phenol by nitrous oxide. Understanding and tuning the ZSM-5 catalyst activities. Top. Catal.13, 387-394. DOI: 10.1023/A:1009015223793.10.1023/A:1009015223793Open DOISearch in Google Scholar

15. Shimizu, A., Tanaka, K., Ogawa, H., Matsuoka, Y., Fujimori, M., Nagamori, Y., Hamachi, H. & Kimura, K. (2003). An Industrial Process for Adipic Acid Production by the Liquid- Phase Oxidation of Cyclohexanone with Molecular Oxygen. Bull. Chem. Soc. Jpn. 76(10), 1993-2001. DOI:10.1246/bcsj.76.1993.10.1246/bcsj.76.1993Search in Google Scholar

16. Kamath, S.S. & Chandalia, S.B. (1973). Liquid phase oxidation of cyclohexanone to adipic acid by air in acetic acid solution. J. Appl. Chem. Biotechnol. 23(6), 469-478. DOI: 10.1002/jctb.5020230610.10.1002/jctb.5020230610Open DOISearch in Google Scholar

17. Rao, D.G. & Raghunathan, T.S. (1984). Oxidation of Cyclohexanone to Adipic Acid with a Cobalt Acetate/Oxygen/ Acetic Acid System. J. Chem. Tech. Biotechnol. 34A, 381-386. DOI: 10.1002/jctb.5040340705.10.1002/jctb.5040340705Open DOISearch in Google Scholar

18. Atlamsani, A., Brégeault, J.M. & Ziyad, M. (1993). Oxidation of 2-Methylcyclohexanone and Cyclohexanone by Dioxygen Catalyzed by Vanadium-Containing Heteropolyanions. J. Org. Chem. 58(21), 5663-5665. DOI: 10.1021/jo00073a026.10.1021/jo00073a026Open DOISearch in Google Scholar

19. Iwahama, T., Syojyo, K., Sakaguchi, S. & Ishii, Y. (1998). Direct Conversion of Cyclohexane into Adipic Acid with Molecular Oxygen Catalyzed by N -Hydroxyphthalimide Combined with Mn(acac) 2 and Co(OAc) 2. Org. Process Res. Dev. 2(4), 255-260. DOI: 10.1021/op980016y.10.1021/op980016yOpen DOISearch in Google Scholar

20. Zou, G., Zhong, W., Mao, L., Xu, Q., Xiao, J., Yin, D., Xiao, Z., Kirk, S.R. & Shu, T. (2015). A non-nitric acid method of adipic acid synthesis: Organic solvent- and promoter-free oxidation of cyclohexanone with oxygen over hollow-structured Mn/TS-1 catalysts. Green Chem. 17(3), 1884-1892. DOI: 10.1039/c4gc02333a.10.1039/c4gc02333aOpen DOISearch in Google Scholar

21. Flemming, W. & Speer W. (1935). U.S. Patent No. 2,005,183.Search in Google Scholar

22. Flemming W. (1942). U.S. Patent No. 2,299,013.Search in Google Scholar

23. Ralph, H.C. & Bergenfield, N.J. (1965). U.S. Patent Np. 3,207,783.Search in Google Scholar

24. Baker R.S., Washington, P. & Cohen M.A. (1966). U.S. Patent Np. 3.234.271.Search in Google Scholar

25. Lidov, R.E. & Neck G.N.Y. (1968). U.S. Patent Np. 3,361,806.Search in Google Scholar

26. Osowska-Pacewicka, K. & Alper, H. (1988). Oxidation of Cyclic Ketones Catalyzed by Polyethylene Glycol and Rhenium Carbonyl under Basic and Exceptionally Mild Conditions, J. Org. Chem. 2(1), 808-810. DOI: 10.1021/jo00239a023.10.1021/jo00239a023Open DOISearch in Google Scholar

27. Besson, M., Gallezot, P., Perrard, A. & Pinel, C. (2005). Active carbons as catalysts for liquid phase reactions. Catal. Today, 102-103, 160-165. DOI: 10.1016/j.cattod.2005.02.037.10.1016/j.cattod.2005.02.037Open DOISearch in Google Scholar

28. Dakkach, M., Atlamsani, A. & Sebti, S. (2012). Le phosphate naturel modifié au vanadium : un nouveau catalyseur pour l’oxydation des cycloalcanones et des α-cétols en présence de l’oxygène moléculaire. C. R. Chimie 15(6), 482-492. DOI: 10.1016/j.crci.2012.03.003.10.1016/j.crci.2012.03.003Open DOISearch in Google Scholar

29. Besson, M., Gauthard, F., Horvath, B. & Gallezot, P. (2005). Catalytic oxidation with air of cyclohexanone to dicarboxylic acids on synthetic carbons. Effect of supported metals and solvents. J. Phys. Chem. B 109(6), 2461-2467. DOI: 10.1021/jp0459662.10.1021/jp045966216851242Open DOISearch in Google Scholar

30. Vennat, M. & Brégeault, J.M. (2010). Oxidative cleavage of cycloalkanones with dioxygen catalyzed by supported catalysts or homogeneous systems: Evidence for novel active ruthenium (II) and/or (III) species. Appl. Catal. A-Gen. 386(1-2), 9-15. DOI: 10.1016/j.apcata.2010.07.016.10.1016/j.apcata.2010.07.016Open DOISearch in Google Scholar

31. Fumagalli, C., Minisci, F. & Pirola, R. (2001). W.O. Patent No. 01,87815. World Intellectual Property Organization.Search in Google Scholar

32. Vennat, M., Bregeault, J.M. & Herson, P. (2004). Mixed crystals containing the dioxo complex [[Ph3SiO]2VO2]- and novel pentacoordinated oxoperoxo complex [[Ph3SiO]2VO- (O2)]-: X-ray crystal structure and assessment as oxidation catalysts. Dalton Trans. (6), 908-13. DOI: 10.1039/b400657g.10.1039/b400657g15252477Open DOISearch in Google Scholar

33. Syroezhko, A.M. & Begak, O.Yu. (2004). Ozonolysis of Methylcyclohexanols and Methylcyclohexanones. Russian J. Appl. Chem. 77(1), 102-105 . DOI: 10.1023/B:RJAC. 0000024586.74168.99.10.1023/B:RJAC.0000024586.74168.99Open DOISearch in Google Scholar

34. Renukdas, S.V., Patil, S. & Patel, N.T. (2014). Kinetics of oxidation of 3-methyl cyclohexanone by periodate catalyzed by Ru(III) in alkaline medium. Physical Chem. 9(4), 141-143.Search in Google Scholar

35. Song, W., Ma, P., Fan, L. & Xiang, Z. (2007). Solubility of Glutaric Acid in Cyclohexanone, Cyclohexanol, Their Five Mixtures and Acetic Acid. Chin. J. Chem. Eng. 15(2), 228-232. DOI: 10.1016/S1004-9541(07)60063-9.10.1016/S1004-9541(07)60063-9Open DOISearch in Google Scholar

eISSN:
1899-4741
Language:
English
Publication timeframe:
4 times per year
Journal Subjects:
Industrial Chemistry, Biotechnology, Chemical Engineering, Process Engineering