Skip to content
Volume 59, Issue 1
  • ISSN: 2056-5135
Preview this article:

There is no abstract available.


Article metrics loading...

Loading full text...

Full text loading...



  1. Sousa-Aguiar E. F., Noronha F. B., and Faro A. Jr Catal. Sci. Technol., 2011, 1, (5), 698 [Google Scholar]
  2. NEXT-GTL Result In Brief, ‘Making Better Use of Natural Gas’, Project Reference 229183, Record Number 91099, Community Research and Development Information Service (CORDIS), Luxembourg, 4th July, 2014 [Google Scholar]
  3. Olah G. A., Goeppert A., and Prakash G. K. S. “Beyond Oil and Gas: The Methanol Economy”, 2nd Edn., Wiley-VCH Verlag GmbH & Co KGaA, Weinheim, Germany, 2009 [Google Scholar]
  4. ‘Periodic Report Summary 2’, Oxidative Coupling of Methane followed by Oligomerisation to Liquids (OCMOL), Project reference 228953, Record Number 53847, Community Research and Development Information Service (CORDIS), Ghent, Belgium, 28th May, 2014 [Google Scholar]
  5. Arutyunov V. S., and Krylov O. V. Russ. Chem. Rev., 2005, 74, (12), 1111 [Google Scholar]
  6. Magomedov R. N., Proshina Yu. A., and Arutyunov V. S. Kinet. Catal., 2013, 54, (4), 383 [Google Scholar]
  7. Magomedov R. N., Proshina Yu. A., Peshnev B. V., and Arutyunov V. S. Kinet. Catal., 2013, 54, (4), 394 [Google Scholar]
  8. Bazhenova T. A., and Shilov A. E. Coord. Chem. Rev., 1995, 144, 69 [Google Scholar]
  9. Johnson Matthey base prices in US$ per troy oz: (Accessed on 24th October 2014)
  10. Savchenko V. I., Makaryan I. A., and Dorokhov V. G. Platinum Metals Rev., 1997, 41, (4), 176 [Google Scholar]
  11. Savchenko V. I., and Makaryan I. A. Platinum Metals Rev., 1999, 43, (2), 74 [Google Scholar]
  12. Shilov A. E., and Shul’pin G. B. Chem. Rev., 1997, 97, (8), 2879 [Google Scholar]
  13. Chukanova O. M., Alpherov K. A., and Belov G. P. J. Mol. Catal. A: Chem., 2010, 325, (1–2), 60 [Google Scholar]
  14. Reppe W., Friederich H., von Kutepow N., Morsch W., and BASF AG ‘Process for the Production of Aliphatic Oxygen Compounds By Carbonylation of Alcohols, Ethers, and Esters’, US Patent 2,729,651; 1956 [Google Scholar]
  15. Haynes A. Adv. Catal., 2010, 53, 1 [Google Scholar]
  16. Behr A., and Neubert P. “Applied Homogeneous Catalysis”, Wiley-VCH Verlag & Co KGaA, Weinheim, Germany, 2012 [Google Scholar]
  17. Moloy K. G., and Petersen J. L. Organometallics, 1995, 14, (6), 2931 [Google Scholar]
  18. Liu B., and Ji S. F. Adv. Mater. Res., 2012, 610–613, 2600 [Google Scholar]
  19. Zoeller J. R. Catal. Today, 2009, 140, (3–4), 118 [Google Scholar]
  20. Haynes A., Maitlis P. M., Morris G. E., Sunley G. J., Adams H., Badger P. W., Bowers C. M., Cook D. B., Elliott P. I. P., Ghaffar T., Green H., Griffin T. R., Payne M., Pearson J. M., Taylor M. J., Vickers P. W., and Watt R. J. J. Am. Chem. Soc., 2004, 126, (9), 2847 [Google Scholar]
  21. ‘Acetic Acid Market for VAM, PTA, Acetate Esters, Acetic Anhydride and Other Applications – Global Industry Analysis, Size, Share, Growth, Trends and Forecast, 2012–2018’, Transparency Market Research, Albany, New York, USA, 3rd October, 2013 [Google Scholar]
  22. ‘Global Acetic Acid Market Estimated to Reach 15.5 Million Tons by 2020’, Plastemart, Mumbai, India, 14th February, 2013 [Google Scholar]
  23. Cheung P., Bhan A., Sunley G. J., and Iglesia E. Angew. Chem. Int. Ed., 2006, 45, (10), 1617 [Google Scholar]
  24. Liu D., Huang X., Hu L., Fang D., Ying W., and Chen D. J. Nat. Gas Chem., 2010, 19, (2), 165 [Google Scholar]
  25. Rizkalla N., and Vale R. The Halcon SD Group, Inc, ‘Preparation of Carboxylic Acid Anhydrides’, US Patent 4,483,803; 1984 [Google Scholar]
  26. Waller F. J. Air Products and Chemicals, Inc, ‘Process for Converting Dimethyl Ether to Ethylidene Diacetate”, European Patent 0,566,371; 1993 [Google Scholar]
  27. Haynes A., and Beller M. ‘Acetic Acid Synthesis by Catalytic Carbonylation of Methanol’, in “Catalytic Carbonylation Reactions”, ed. Topics in Organometallic Chemistry, Springer-Verlag, Berlin, Heidelberg, Germany, 2006, Vol. 18, pp. 179205 [Google Scholar]
  28. Roelen O. ‘Verfahren zur Herstellung von sauerstoffhaltigen Verbindungen’, German Patent 849,548; 1938 [Google Scholar]
  29. Cornils B., Herrmann W. A., and Rasch M. Angew. Chem. Int. Ed., 1994, 33, (21), 2144 [Google Scholar]
  30. Wiese K.-D., Obst D., and Beller M. ‘Hydroformylation’, in “Catalytic Carbonylation Reactions”, ed. Topics in Organometallic Chemistry, Springer-Verlag, Berlin, Heidelberg, Germany, 2006, Vol. 18, pp. 133 [Google Scholar]
  31. Cornils B., and Herrmann W. A. “Aqueous-Phase Organometallic Catalysis: Concepts and Applications”, 2nd Edn., eds. Wiley-VCH Verlag GmbH & Co KGaA, Weinheim, Germany, 2004 [Google Scholar]
  32. Belov G. P., and Novikova E. V. Russ. Chem. Rev., 2004, 73, (3), 267 [Google Scholar]
  33. Drent E., and Budzelaar P. H. M. Chem. Rev., 1996, 96 , (2), 663 [Google Scholar]
  34. Seifert H. Kunststoffe, 1998, 88, 1154 [Google Scholar]
  35. Garbassi F. Chemtech, 1999, 29, (10), 48 [Google Scholar]
  36. ‘Polyketone returns’, Injection World, November/December 2013, p. 36 [Google Scholar]
  37. Eastham G. R., Tooze R. P., Kilner M., Foster D. F., and Cole-Hamilton D. J. J. Chem. Soc. Dalton Trans., 2002, (8), 1613 [Google Scholar]
  38. Zudin V. N., Il’inich G. N., Likholobov V. A., and Yermakov Y. I. J. Chem. Soc., Chem. Commun., 1984, (8), 545 [Google Scholar]
  39. Cavinato G., Toniolo L., Vavasori A., and Beller M. ‘Carbonylation of Ethene in Methanol Catalysed by Cationic Phosphine Complexes of Pd(II): from Polyketones to Monocarbonylated Products’, in “Catalytic Carbonylation Reactions”, ed. Topics in Organometallic Chemistry, Springer-Verlag, Berlin, Heidelberg, Germany, 2006, Vol. 18, pp. 125164 [Google Scholar]
  40. Robertson R. A. M., and Cole-Hamilton D. J. Coord. Chem. Rev., 2002, 225, (1–2), 67 [Google Scholar]
  41. Harris B. ‘Acrylics for the Future’, Ingenia, December 2010, Issue 45, p. 19 [Google Scholar]
  42. van Leeuwen M. P. W. N., Freixa Z., and Kollár L. ‘Bite Angle Effects of Diphosphines in Carbonylation Reactions’, in “Modern Carbonylation Methods”, ed. Wiley-VCH Verlag GmbH & Co KGaA, Weinheim, Germany, 2008 [Google Scholar]
  43. ‘Methyl Methacrylate: A Global Strategic Business Report’, Global Industry Analysts Inc, San Jose, California, USA, February, 2013 [Google Scholar]
  44. Morimoto T., and Kakiuchi K. Angew. Chem. Int. Ed., 2004, 43, (42), 5580 [Google Scholar]
  45. He L., Liu H., Xiao C.-x., and Kou Y. Green Chem., 2008, 10, (6), 619 [Google Scholar]
  46. Roscher G. ‘Vinyl Esters’ in “Ullmans’s Encyclopedia of Industrial Chemistry”, Wiley-VCH Verlag GmbH & Co KGaA, Weinheim, Germany, 2007 [Google Scholar]
  47. Bitzzari S. N., Gubler R., and Kishi A. ‘Oxo Chemicals’, in “Chemical Economics Handbook”, SRI International, Report number 682.7000, 2002, pp. 1121 [Google Scholar]
  48. Weissermel K., and Arpe H.-J. “Industrial Organic Chemistry”, 4th Edn., Wiley-VCH Verlag GmbH & Co KGaA, Weinheim, Germany, 2003 [Google Scholar]
  49. Conn I. ‘Refining & Marketing Welcome’, Refining and Marketing Investor Day, BP Plc, Pangbourne, UK, 30th November, 2011 [Google Scholar]
  50. Moiseev I. I., Vargaftik M. N., and Syrkin Ya. K. Dokl. Akad. Nauk SSSR, 1960, 133, 377 [Google Scholar]
  51. Fernholz H., Schmidt H.-J., Wunder F., and Hoechst AG ‘Process for the Manufacture of Vinyl Esters of Carboxylic Acids’, German Patent 1,296,138; 1967 [Google Scholar]
  52. Robinson R. E. National Distillers, ‘Process for Preparing Esters’, US Patent 3,190,912; 1965 [Google Scholar]
  53. Brulé E., Guo J., Coates G. W., and Thomas C. M. Macromol. Rapid Comm., 2011, 32, (2), 169 [Google Scholar]
  54. Eastham G. R., Waugh M., and Richards P. I. Lucite International UK Limited, ‘Carbonylation of Ethylenically Unsaturated Compounds’, World Appl. 2007/057,640 [Google Scholar]
  55. Savchenko V. I., Makaryan I. A., Fokin I. G., Sedov I. V., Magomedov R. N., Lipilin M. G., and Arutyunov V. S. Neftepererabotka i Neftechimiya, 2013, (8), 21 [Google Scholar]
  56. Arutyunov V. “Direct Methane to Methanol: Foundations and Prospects of the Process”, Elsevier BV, Amsterdam, The Netherlands, 2014 [Google Scholar]
  57. Arutyunov V. S., Sheverdenkin E. V., Rudakov V. M., and Savchenko V. I. Stud. Surf. Sci. Catal., 2004, 147, 703 [Google Scholar]
  58. Arutyunov V. S., and Magomedov R. N. Russ. Chem. Rev., 2012, 81, (9), 790 [Google Scholar]
  59. Wood D. A., Nwaoha C., and Towler B. F. J. Nat. Gas Sci. Eng., 2012, 9, 196 [Google Scholar]
  60. Steynberg A. P., Espinoza R. L., Jager B., and Vosloo A. C. Appl. Catal. A: Gen., 1999, 186, (1–2), 41 [Google Scholar]

Data & Media loading...

  • Article Type: Research Article
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error