Skip to main content
Log in

Catalysts Based on High-Vanadium Solutions of Molybdovanadophosphoric Heteropolyacids: Achievements, Challenges, and Prospects

  • Published:
Kinetics and Catalysis Aims and scope Submit manuscript

Abstract

A retrospective review based on the authors’ work is devoted to homogeneous catalytic systems based on aqueous solutions of Mo–V–P heteropolyacids (HPA-x, x is the number of vanadium atoms). These catalytic systems were first proposed for oxidative reactions at Boreskov Institute of Catalysis. The properties of HPA-x solutions, methods for their synthesis, promising processes occurring in their presence, problems related to the use of these solutions, and ways of solving these problems are considered. Prospects for the creation of industrial processes based on modified high-vanadium HPA-x solutions of non-Keggin compositions are shown.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1.
Fig. 2.
Fig. 3.
Fig. 4.
Fig. 5.
Fig. 6.
Fig. 7.
Fig. 8.

Similar content being viewed by others

REFERENCES

  1. Kozhevnikov, I.V. and Matveev, K.I., Usp. Khim., 1982, vol. 51, no. 11, p. 1875.

    Article  CAS  Google Scholar 

  2. Kozhevnikov, I.V. and Matveev, K.I., Appl. Catal., 1983, vol. 5, no. 2, p. 135.

    Article  CAS  Google Scholar 

  3. Pope, M.T. and Muller, A., Angew. Chem., Int. Ed., 1991, vol. 30, p. 34.

    Article  Google Scholar 

  4. Misono, M. and Nojiri, N., Appl. Catal., 1990, vol. 64, p. 1.

    Article  CAS  Google Scholar 

  5. Mizuno, N. and Misono, M., J. Mol. Catal., 1994, vol. 86, nos. 1–3, p. 319.

    Article  CAS  Google Scholar 

  6. Hill, C.L. and Prosser-McCartha, C.M., Coord. Chem. Rev., 1995, vol. 143, nos. 1–2, p. 407.

    Article  CAS  Google Scholar 

  7. Okuhara, T., Mizuno, N., and Misono, M., Adv. Catal., 1996, vol. 41, nos. 1–3, p. 113.

    CAS  Google Scholar 

  8. Kozhevnikov, I.V., Chem. Rev., 1998, vol. 98, no. 1–2, p. 171.

    Article  CAS  PubMed  Google Scholar 

  9. Okuhara, T., Mizuno, N., and Misono, M., Appl. Catal., A, 2001, vol. 222, no. 1, p. 63.

  10. Kozhevnikov, I.V., Catalysis by Polyoxometalates, Chichester: John Wiley, 2002, p. 202.

    Google Scholar 

  11. López, X., Carbó, J.J., Bo, C., and Poblet, J.M., Chem. Soc. Rev., 2012, vol. 41, p. 7537.

    Article  PubMed  CAS  Google Scholar 

  12. Zhou, Yu, Guo, Z., Hou, W., Wang, Q., and Wang, J., Catal. Sci. Technol., 2015, vol. 5, p. 4324.

    Article  CAS  Google Scholar 

  13. Wang, S.S. and Yang, G.Yu., Chem. Rev., 2015, vol. 115, p. 4893.

    Article  CAS  PubMed  Google Scholar 

  14. Rodikova, Yu.A., Zhizhina, E.G., and Pai, Z.P., Chem. Sel., 2016, vol. 1, p. 2113.

    CAS  Google Scholar 

  15. Kale, S.S., Armbruster, U., Eckelt, R., Bentrup, U., Umbarkar, S.B., Dongare, M.K., and Martin, A., Appl. Catal., A, 2016, vol. 527, p. 9.

  16. USSR Inventor’s Certificate no. 421226, 1992.

  17. DBR Patent 1154798, 1963.

  18. Cavani, F., Catal. Today, 1998, vol. 41, no. 1, p. 73.

    Article  CAS  Google Scholar 

  19. Sano, K., Uchida, H., and Wakabayashi, S., Catal. Surv. Japan, 1999, vol. 3, p. 55.

    Article  CAS  Google Scholar 

  20. Kozhevnikov, I.V., Chem. Rev., 1993, vol. 62, nos. 1–2, p. 510.

    CAS  Google Scholar 

  21. RF Patent 2165406, 2001.

  22. RF Patent 2162837, 2001.

  23. Kozhevnikov, I.V., Usp. Khim., 1987, vol. 56, no. 9, p. 1417.

    Article  CAS  Google Scholar 

  24. Pope, M.T., Heteropoly and Isopoly Oxometalates, Berlin: Spring, 1983, p. 238.

  25. Odyakov, V.F., Zhizhina, E.G., and Matveev, K.I., Russ. J. Inorg. Chem., 2000, vol. 45, no. 8, p. 1258.

    Google Scholar 

  26. Souchay, P., Ions Mineraux Condencer, Paris: Masson, 1969, p. 287.

    Google Scholar 

  27. Weakly, T.J.R., Struct. Bonding, 1974, vol. 18, p. 131.

    Article  Google Scholar 

  28. Kazanskii, L.P., Torchenkova, E.A., and Spitsyn, V.I., Usp. Khim., 1974, vol. 43, p. 1137.

    Article  CAS  Google Scholar 

  29. Courtin, P., Chauveau, F., and Souchay, P.S, C. R. Acad. Sci., 1964, vol. 258, p. 1247.

    CAS  Google Scholar 

  30. Courtin, P., Rev. Chim. Miner., 1971, vol. 8, p. 75.

    CAS  Google Scholar 

  31. Porai-Koshits, M.A. and Atovmyan, L.O., Koord. Khim., 1975, vol. 1, no. 6, p. 1271.

    CAS  Google Scholar 

  32. Grate, J.H., J. Mol. Catal. A: Chem., 1996, vol. 114, nos. 1–3, p. 93.

    Article  CAS  Google Scholar 

  33. Souchay, P. and Courtin, P., C. R. Acad. Sci., 1970, vol. 27OC, p. 1714.

    Google Scholar 

  34. Fedotov, M.A. and Maksimovskaya, R.I., Dokl. Akad. Nauk SSSR, 1978, vol. 240, no. 1, p. 128.

    CAS  Google Scholar 

  35. Maksimovskaya, R.I., Fedotov, M.A., Mastikhin, V.M., Kuznetsova, L.I., and Matveev, K.I., In Study of the Properties and Application of Heteropoly Acids in Catalysis, 1978, p. 140.

    Google Scholar 

  36. Maksimovskaya, R.I., Fedotov, M.A., Mastikhin, V.M., Kuznetsova, L.I., and Matveev, K.I., Dokl. Akad. Nauk SSSR, 1978, vol. 240, no. 1, p. 117.

    CAS  Google Scholar 

  37. Kholdeeva, O.A. and Maksimovskaya, R.I., Zh. Neorg. Khim., 1992, vol. 37, no. 6, p. 1349.

    CAS  Google Scholar 

  38. Maksimovskaya, R.I., Fedotov, M.A., Kuznetsova, L.I., Mastikhin, N.M., and Matveev, K.I., Dokl. Akad. Nauk SSSR, 1975, vol. 223, no. 2, p. 385.

    CAS  Google Scholar 

  39. Sergienko, V.S., Porai-Koshits, M.A., Fedotov, M.A., Yurchenko, E.N., and Kuznetsova, L.I., Zh. Strukt. Khim., 1977, vol. 18, no. 5, p. 976.

    CAS  Google Scholar 

  40. Sergienko, V.S., Porai-Koshits, M.A., and Yurchenko, E.N., Zh. Strukt. Khim., 1980, vol. 21, no. 1, p. 111.

    CAS  Google Scholar 

  41. Klevtsova, R.F., Yurchenko, E.N., Glinskaya, L.A., Detusheva, L.G., and Kuznetsova, L.I., Zh. Strukt. Khim., 1981, vol. 22, no. 1, p. 49.

    CAS  Google Scholar 

  42. Yurchenko, E.N., Solov’eva, L.P., Klevtsova, R.F., Detusheva, L.G., and Glinskaya, L.A., Zh. Strukt. Khim., 1985, vol. 26, no. 1, p. 118.

    CAS  Google Scholar 

  43. Fedotov, M.A., Maksimovskaya, R.A., and Kazanskii, L.P., React. Kinet. Catal. Lett., 1981, vol. 16, no. 1, p. 185.

    Article  CAS  Google Scholar 

  44. Yurchenko, E.N., Metody molekulyarnoi spektroskopii v khimii koordinatsionnykh soedinenii i katalizatorov (Methods of Molecular Spectroscopy in Chemistry of Coordination Compounds and Catalysts), Novosibirsk: Nauka, 1976.

  45. Maksimovskaya, R.I., Kuznetsova, L.I., and Matveev, K.I., Koord. Khim., 1977 vol. 3, no. 3, p. 685.

    CAS  Google Scholar 

  46. Yurchenko, E.N., Metody molekulyarnoi spektroskopii v khimii koordinatsionnykh soedinenii i katalizatorov (Methods of Molecular Spectroscopy in Chemistry of Coordination Compounds and Catalysts), Novosibirsk: Nauka, 1976.

  47. Bruckman, K., Haber, J., Serwicka, E.M., Yurchenko, E.N., and Lazarenko, T.P., Catal. Lett., 1990, vol. 4, p. 181.

    Article  CAS  Google Scholar 

  48. Kato, R., Kobajashi, A., and Sasaky, Y., J. Am. Chem. Soc., 1980, vol. 102, p. 6571.

    Article  CAS  Google Scholar 

  49. Yurchenko, E.N., Metody molekulyarnoi spektroskopii v khimii koordinatsionnykh soedinenii i katalizatorov (Molecular Spectroscopy Methods in the Chemistry of Coordination Compounds and Catalysts), Novosibirsk: Nauka, 1976, p. 100.

  50. Pettersson, L., The International Workshop Polyoxometalates, Dordrecht: Kluwer Academic Publishers, 1993, p. 27.

  51. Kuznetsova, L.I., Yurchenko, E.N., Maksimovskaya, R.I., and Matveev, K.I., Koord. Khim., 1976, vol. 2, no. 1, p. 67.

    CAS  Google Scholar 

  52. Kuznetsova, L.I., Yurchenko, E.N., Maksimovskaya, R.I., Kirik, N.P., and Matveev, K.I., Koord. Khim., 1977, vol. 3, no. 1, p. 51.

    CAS  Google Scholar 

  53. Maksimovskaya, R.I., in Issledovanie svoistv i primenenie geteropolikislot v katalize (Study of Properties and Application of Heteropoly Acids in Catalysis), Novosibirsk, 1978, p. 177.

  54. Detusheva, L.G., Yurchenko, E.N., and Tkachev, S.V., Koord. Khim., 1983, vol. 9, no. 9, p. 1220.

    CAS  Google Scholar 

  55. Pope, M.T. and Scully, T.F., Inorg. Chem., 1975, vol. 14, no. 5, p. 953.

    Article  CAS  Google Scholar 

  56. Maksimovskaya, R.I., Fedotov, M.A., Kuznetsova, L.I., Mastikhin, N.M., and Matveev, K.I., Dokl. Akad. Nauk SSSR, 1975, vol. 223, no. 2, p. 385.

    CAS  Google Scholar 

  57. Pope, M.T., O’Donnell, S.E., and Prados, R.A., J. Chem. Soc., Chem. Commun., 1975, no. 1, p. 22.

  58. Souchay, P., Chauveau, F., and Courtin, P., Bull. Soc. Chim. France, 1968, no. 6, p. 2384.

  59. Detusheva, L.G. and Yurchenko, E.N., Koord. Khim., 1982, vol. 8, no. 7, p. 948.

    CAS  Google Scholar 

  60. Detusheva, L.G. and Yurchenko, E.N., Koord. Khim., 1990, vol. 16, no. 7, p. 930.

    CAS  Google Scholar 

  61. Burov, Yu.V., Kozhevnikov, I.V., Matveev, K.I., and Belyaev, V.D., Izv. Akad. Nauk SSSR, Ser. Khim., 1980, no. 7, p. 1469.

  62. Zhizhina, E.G., Kuznetsova, L.I., Yurchenko, E.N., and Matveev, K.I., Koord. Khim., 1980, vol. 6, no. 12, p. 1846.

    CAS  Google Scholar 

  63. Maksimovskaya, R.I. and Chumachenko, N.N., Polyhedron, 1987, vol. 6, no. 10, p. 1813.

    Article  CAS  Google Scholar 

  64. Maksimov, G.M., Usp. Khim., 1995, vol. 64, no. 5, p. 480.

    Article  CAS  Google Scholar 

  65. Tsigdinos, G.A. and Hallada, G.J., Inorg. Chem., 1968, vol. 7, no. 2, p. 437.

    Article  CAS  Google Scholar 

  66. Polotebnova, N.A., Nguen Van Cheu, and Kal’nibolotskaya, V.V, Zh. Neorg. Khim., 1973, vol. 18, no. 2, p. 413.

    CAS  Google Scholar 

  67. Charreton, B. and Bertho, G., Comptes Rendus Hebdomadaires des Seances de l’Academie des Sciences, 1965, vol. 261, no. 15, p. 2903.

    CAS  Google Scholar 

  68. Odyakov, V.F., Zhizhina, E.G., Maximovskaya, R.I., and Matveev, K.I., Kinet. Catal., 1995, vol. 36, no. 5, p. 733.

    CAS  Google Scholar 

  69. Maksimov, G.M., Maksimovskaya, R.I., and Kozhevnikov, I.V., Zh. Neorg. Khim., 1994, vol. 39, no. 4, p. 623.

    CAS  Google Scholar 

  70. Odyakov, V.F., Zhizhina, E.G., Rodikova, Yu.A., and Gogin, L.L., Eur. J. Inorg. Chem., 2015, vol. 2015, no. 22, p. 3618.

    Article  CAS  Google Scholar 

  71. RF Patent 2230612, 2004.

  72. Matveev, K.I., Zhizhina, E.G., Odyakov, V.F., and Parmon, V.N., Catal. Ind., 2014, vol. 6, no. 3, p. 202.

    Article  Google Scholar 

  73. Odyakov, V.F., Zhizhina, E.G., Matveev, K.I., and Parmon, V.N., Catal. Ind., 2015, vol. 7, no. 2, p. 111.

    Article  Google Scholar 

  74. Rodikova, Y.A. and Zhizhina, E.G., Catal. Ind., 2019, vol. 11, no. 3, p. 179.

    Article  Google Scholar 

  75. Timofeeva, M.N., Appl. Catal., A, 2003, vol. 256, nos. 1–2, p. 19.

  76. Fedotov, M.A., Maksimov, G.M., and Ignashin, S.V., Russ. J. Inorg. Chem., 2002, vol. 47, no. 12, p. 1867.

    Google Scholar 

  77. Maksimov, G.M. and Golovin, A.V., Russ. J. Inorg. Chem., 2004, vol. 49, no. 8, p. 1256.

    Google Scholar 

  78. Okuhara, T., Kimura, M., Kawai, T., Xu, Z., and Nakato, T., Catal. Today, 1998, vol. 45, nos. 1–4, p. 73.

    Article  CAS  Google Scholar 

  79. Izumi, Y., Catal. Today, 1997, vol. 33, no. 4, p. 371.

    Article  CAS  Google Scholar 

  80. Khankhasaeva, S.Ts., Kulikov, S.M., and Kozhevnikov, I.V., Kinet. Katal., 1990, vol. 31, no. 1, p. 216.

    CAS  Google Scholar 

  81. Kozhevnilkov, I.V., Kulikov, S.M., Chukaeva, N.G., Kirsanov, A.T., Letunova, A.B., and Blinova, V.I., React. Kinet. Catal. Lett., 1992, vol. 47, no. 1, p. 59.

    Article  Google Scholar 

  82. Meuzelaar, G.J., Maat, L., Sheldon, R.A., and Kozhevnikov, I.V., Catal. Lett., 1997, vol. 45, p. 249.

    Article  CAS  Google Scholar 

  83. Bardin, B.B. and Davis, R.J., Appl. Catal., A, 2000, vol. 200, no. 1–2, p. 219.

  84. Hayashi, H. and Moffat, J.B., J. Catal., 1982, vol. 77, no. 2, p. 473.

    Article  CAS  Google Scholar 

  85. Gayraud, P.Y., Stewart, I.H., Derouane-Abd Hamid, S.B., Essayem, N.E., Derouane, E.G., and Vedrine, J.C., Catal. Today, 2000, vol. 63, no. 2, p. 223.

    Article  CAS  Google Scholar 

  86. Vaughan, J.S., Oconnor, C.T., and Fletcher, J.C.Q., J. Catal., 1994, vol. 147, no. 2, p. 441.

    Article  CAS  Google Scholar 

  87. Okuhara, T., Nishimura, T., Wanatabe, H., and Misono, M., J. Mol. Catal., 1992, vol. 74, nos. 1–3, p. 247.

    Article  CAS  Google Scholar 

  88. Matveev, K.I., Zhizhina, E.G., Shitova, N.B., and Kuznetsova, L.I., Kinet. Katal., 1977, vol. 18, no. 2, p. 380.

    CAS  Google Scholar 

  89. Matveev, K.I., Zhizhina, E.G., Odyakov, V.F., and Parmon, V.N., Russ. Chem. Bull., 1994, vol. 43. Is. 7, p. 1142.

  90. Matveev K.I., Odyakov V.F., and Zhizhina E.G., J. Mol. Catal. A: Chem., 1996, vol. 114, nos. 1–3, p. 151.

    Article  CAS  Google Scholar 

  91. Odyakov, V.F., Kuznetsova, L.I., and Matveev, K.I., Zh. Neorg. Khim., 1978, vol. 23, no. 2, p. 457.

    CAS  Google Scholar 

  92. Alimarin, I.P., Dorokhova, E.N., Kazanskii, L.P., and Prokhorova, G.V., Zh. Anal. Khim., 1980, vol. 35, no. 10, p. 2000.

    CAS  Google Scholar 

  93. Khyarsing, I.V. and Filippov, A.P., Zh. Neorg. Khim., 1988, vol. 33, no. 5, p. 900.

    Google Scholar 

  94. Kaszonyi, A., Hronec, M., and Harustiak, M., J. Mol. Catal., 1993, vol. 80, no. 3, p. L13.

    Article  CAS  Google Scholar 

  95. Bard, A.J., Parsons, R., and Jordan, J., Standard Potentials in Aqueous Solution (IUPAC), New York–Basel: Marcer Dekker, 1985, p. 4.

    Google Scholar 

  96. Matveev, K.I., in Issledovanie svoistv i primenenie geteropolikislot v katalize (Study of Properties and Application of Heteropoly Acids in Catalysis), Novosibirsk, 1978, p. 3.

  97. Zhizhina, E.G., Kuznetsova, L.I., and Matveev, K.I., Kinet. Katal., 1988, vol. 29, no. 1, p. 130.

    CAS  Google Scholar 

  98. Bard, A.J., Parsons, R., and Jordan, J., Standard Potentials in Aqueous Solution (IUPAC), New York: Marcer Dekker, 1985, p. 507.

    Google Scholar 

  99. Zhizhina, E.G., Odyakov, V.F., and Matveev, K.I., Russ. J. Appl. Chem., 2000, vol. 73, no. 5, p. 824.

    Google Scholar 

  100. Jira, R., Blau, W., and Grimm, D., Hydrocarbon Process., 1976, vol. 55, no. 3, p. 97.

    Google Scholar 

  101. Zhizhina, E.G., Odyakov, V.F., Simonova, M.V., and Matveev, K.I., Kinet. Catal., 2005, vol. 46, no. 3, p. 354.

    Article  CAS  Google Scholar 

  102. Novyi spravochnik khimika i tekhnologa. Obshchie svedeniya i dr (New Handbook of Chemist and Technologist. General Information etc.), St. Petersburg: NPO “Professional,” 2006, vol. 12, p. 309.

  103. Yurchenko, E.N., Matvienko, L.G., Kuznetsova, L.I, Pankratiev, Yu.D., and Matveev, K.I., React. Kinet. Catal. Lett., 1976, vol. 4, no. 2, p. 405.

    Article  CAS  Google Scholar 

  104. Filippov, A.P. and Khyarsing, I.V., Zh. Neorg. Khim., 1978, vol. 23, no. 8, p. 1523.

    CAS  Google Scholar 

  105. Zhizhina, E.G., Pankrat’ev, Yu.D., Odyakov, V.F., and Matveev, K.I., Zh. Neorg. Khim., 1999, vol. 44, no. 4, p. 561.

    CAS  Google Scholar 

  106. Zhizhina, E.G., Odyakov, V.F., and Matveev, K.I., Eur. J. Inorg. Chem., 1999, no. 6, p. 1009.

  107. Calvet, E. and Prat, A., Recent Progress in Microcalorimetry, Pergamon, 1963, p. 190.

    Google Scholar 

  108. Blanc, P., Madic, C., and Launay, J.P., Inorg. Chem., 1982, vol. 21, no. 8, p. 2923.

    Article  CAS  Google Scholar 

  109. Pletnev, R.N., Ivakin, A.A., Gorshkov, V.V., and Chirkov, A.K., Dokl. Akad. Nauk SSSR, 1975, vol. 224, no. 1, p. 106.

    CAS  Google Scholar 

  110. Sasaki, Yu., Nippon kesshogaku kaishi (J. Crystallogr. Soc. Jpn), 1975, vol. 17, no. 2, p. 127.

  111. Kirkegaard, P. and Longo, J.M., Acta Chem. Scand., 1965, vol. 19, no. 8, p. 1906.

    Article  Google Scholar 

  112. Odyakov, V.F., Zhizhina, E.G., Maksimovskaya, R.I., and Matveev, K.I., Russ. J. Inorg. Chem., 1998, vol. 43, no. 9, p. 1338.

    Google Scholar 

  113. Zhizhina, E.G. and Odyakov, V.F., Appl. Catal., A, 2009, vol. 358, p. 254.

  114. Zhizhina, E.G. and Odyakov, V.F., React. Kinet. Catal. Lett., 2008, vol. 95, no. 2, p. 301.

    Article  CAS  Google Scholar 

  115. Odyakov, V.F., Zhizhina, E.G., and Maksimovskaya, R.I., Appl. Catal., A, 2008, vol. 342, p. 126.

  116. Baes, C.A. and Mesmer, R.E., The Hydrolysis of Cations, New York: Wiley, 1976, p. 210.

    Google Scholar 

  117. Sadakane, M. and Steckhan, E., Chem. Rev., 1998, vol. 98. Is.1, p. 219.

  118. Filippov, A.P., Härsing, I., Kirjanen, E., and Kirjanen, I., Eesti NSV Tead. Akad. Toim. Keemia. 1981, vol. 30, p. 235 (in Russian).

    CAS  Google Scholar 

  119. Blanc, P., Madic, C., and Launay, J.P., Inorg. Chem., 1982, vol. 21, p. 2923.

    Article  CAS  Google Scholar 

  120. Jenkins, H.D.B. and Marcus, Y., Chem. Rev., 1995, vol. 95, p. 2695.

    Article  CAS  Google Scholar 

  121. Zhizhina, E.G., Simonova, M.V., Odyakov, V.F., and Matveev, K.I., Appl. Catal., A, 2007, vol. 319, p. 91.

  122. Rodikova, Yu.A. and Zhizhina, E.G., Kinet. Catal., 2019, vol. 60, no. 6, p. 790.

    Article  CAS  Google Scholar 

  123. Zhizhina, E.G., Simonova, M.V., Odyakov, V.F., and Matveev, K.I., Katal. Prom-sti., 2005, vol. 2, p. 17.

    Google Scholar 

  124. A New Handbook of Chemistry and Chemical Engineering. Electrolytic Processes, St.-Petersburg: NPO “Professional,” 2004, p. 114.

  125. Zhizhina, E.G. and Odyakov, V.F., React. Kinet. Catal. Lett. 2009, vol. 98, no. 1, p. 51.

    Article  CAS  Google Scholar 

  126. GOST 5632‑72.

  127. Zhizhina, E.G., Kuznetsova, L.I., and Matveev, K.I., Kinet. Katal., 1984, vol. 25, no. 5, p. 1095.

    CAS  Google Scholar 

  128. Kuznetsova, L.I., Matveev, K.I., and Zhizhina, E.G., Kinet. Katal., 1985, vol. 26, no. 5, p. 1029.

    CAS  Google Scholar 

  129. Zhizhina, E.G., Matveev, K.I., and Kuznetsova, L.I., Kinet. Katal., 1985, vol. 26, no. 2, p. 461.

    CAS  Google Scholar 

  130. Zhizhina, E.G., Kuznetsova, L.I., and Matveev, K.I., Kinet. Katal., 1985, vol. 26, no. 7, p. 1349.

    CAS  Google Scholar 

  131. Zhizhina, E.G., Kuznetsova, L.I., and Matveev, K.I., React. Kinet. Catal. Lett., 1986, vol. 31, no. 1, p. 113.

    Article  CAS  Google Scholar 

  132. Zhizhina, E.G., Kuznetsova, L.I., and Matveev, K.I., Kinet. Katal., 1988, vol. 29, no. 1, p. 130.

    CAS  Google Scholar 

  133. USSR Inventor’s Certificate no. 1027880, 1995.

  134. Zhizhina, E.G., Kuznetsova, L.I., Maksimovskaya, R.I., Pavlova, S.N., and Matveev, K.I., J. Mol. Catal., 1986, vol. 38, nos. 1–2, p. 345.

    Article  CAS  Google Scholar 

  135. Pavlova, S.N., Kuznetsova, L.I., Matveev, K.I., Sazonov, V.A., Popovskii, V.V., Zhizhina, E.G., Fenelonov, V.B., and Gavrilov, V.Yu., Kinet. Katal., 1987, vol. 28, no. 2, p. 373.

    CAS  Google Scholar 

  136. USSR Inventor’s Certificate no. 1135054, 1994.

  137. Matveev, K.I., Shitova, N.B., and Zhizhina, E.G., Kinet. Katal., 1976, vol. 17, no. 4, p. 893.

    CAS  Google Scholar 

  138. Zhizhina, E.G., Shitova, N.B., and Matveev, K.I., Kinet. Katal., 1981, vol. 22, no. 6, p. 1451.

    CAS  Google Scholar 

  139. USSR Inventor’s Certificate no. 1669109, 1989.

  140. Zhizhina, E.G., Simonova, M.V., Odyakov, V.F., and Matveev, K.I., React. Kinet. Catal. Lett., 2003, vol. 80, no. 1, p. 171.

    Article  CAS  Google Scholar 

  141. Zhizhina, E.G., Odyakov, V.F., Balashov, A.L., and Matveev, K.I., Katal. Prom-sti, 2005, no. 5, p. 28.

  142. RF Patent 2230612, 2004.

  143. RF Patent 2243818, 2005.

  144. RF Patent 2275960, 2006.

  145. Odyakov, V.F., Titova, T.F., Matveev, K.I., and Krysin, A.P., Khim.-Farm. Zh., 1992, vol. 26, no. 7–8, p. 69.

    CAS  Google Scholar 

  146. Shnaidman, L.O., Proizvodstvo vitaminov. 2-e izd (Production of Vitamines, 2nd ed.), Moscow: Pishchepromizdat, 1973.

  147. USSR Inventor’s Certificate no. 2022958, 1994.

  148. RF Patent 2061669, 1996.

  149. RF Patent 2142935, 1999.

  150. Matveev, K.I., Zhizhina, E.G., and Odyakov, V.F., Khim. Prom-st., 1996, no. 3, p. 173.

  151. RF Patent 2050345, 1995.

  152. RF Patent 2126792, 1999.

  153. Matveev, K.I., Zhizhina, E.G., Odyakov, V.F., Kotsarenko, N.S., and Shmachkova, V.P., Kinet. Catal., 1997, vol. 38, no. 1, p. 64.

    CAS  Google Scholar 

  154. Mercier, C. and Chabardes, P., Pure Appl. Chem., 1994, vol. 66, no. 7, p. 1509.

    Article  CAS  Google Scholar 

  155. DR Patent 2221624, 1972.

  156. EP Patent 0127888, 1984.

  157. Jpn. Patent 56140946, 1981.

  158. Jpn. Patent 60255745, 1985.

  159. EP Patent 27888, 1987.

  160. EP Patent 0475272, 1992.

  161. IN Patent 181827, 1998.

  162. Bard, A.J., Parsons, R., and Jordan, J., Standard Potentials in Aqueous Solution (IUPAC), New York–Basel: Marcer Dekker, 1985, p. 292.

    Google Scholar 

  163. Lissel, M., Jansen, W., and Neumann, R., Tetrahedron Lett., 1992, vol. 33, no. 13, p. 1795.

    Article  CAS  Google Scholar 

  164. USSR Patent 1719392, 1992.

  165. Kholdeeva, O.A., Golovin, A.V., and Kozhevnikov, I.V., React. Kinet. Catal. Lett., 1992, vol. 6, p. 107.

    Article  Google Scholar 

  166. Zhizhina, E.G., Odyakov, V.F., and Matveev, K.I., Katal. Prom-sti., 2005, no. 6, p. 19.

  167. Rodikova, Yu.A. and Zhizhina, E.G., Izv. Vyssh. Uchebn. Zaved., Fiz., 2011, no. 12/2, p. 86.

  168. Rodikova, Yu.A. and Zhizhina, E.G., Chem. Sust. Dev., 2012, vol.20, no. 6, p. 605.

    Google Scholar 

  169. Rodikova, Yu.A. and Zhizhina, E.G., J. Chem. Chem. Eng., 2013, vol. 7, no. 9, p. 808.

    CAS  Google Scholar 

  170. Rodikova, Yu.A. and Zhizhina, E.G., Katal. Prom-sti., 2019, vol.6, no. 1, p. 243.

    Google Scholar 

  171. Finley, K.T., The Chemistry of the Quinonoid Compounds, vol. II. Part 1, Patai, S. and Rappoport, Z., Eds., New York: Wiley, 1988, p. 537.

  172. Dauben, W.G., Farkas, I., Bridon, D.P., Chuang, C.P., and Henegar, K.E., J. Am. Chem. Soc., 1991, vol. 113, no. 15, p. 5883.

    Article  CAS  Google Scholar 

  173. Liu, C., Bao, G., and Burnell, D.J., J. Chem. Soc., Perkin Trans., 2001, vol. 9, p. 2644.

    Article  Google Scholar 

  174. Schuber, M. and Metz, P., Angew. Chem., 2011, vol. 123, no. 13, p. 3011.

    Article  Google Scholar 

  175. Zhao, L. and Burnell, D.J., Org. Lett., 2006, vol. 8, no. 1, p. 155.

    Article  CAS  PubMed  Google Scholar 

  176. Shiraishi, S., Ikeuchi, S., Senō, M., and Asahara, T., Bull. Chem. Soc. Jpn., 1978, vol. 51, no. 3, p. 921.

    Article  CAS  Google Scholar 

  177. Parker, K.A., Cohen, I.D., Padwa, A., and Dent, W., Tetrahedron Lett., 1984, vol. 25, no. 43, p. 4917.

    Article  CAS  Google Scholar 

  178. Yadav, J.S., Reddy, B.V.S., and Swamy, T., Tetrahedron Lett., 2003, vol. 44, no. 26, p. 4861.

    Article  CAS  Google Scholar 

  179. Mothe, S.R., Susanti, D., and Chan, P.W.H., Tetrahedron Lett., 2010, vol. 51, no. 16, p. 2136.

    Article  CAS  Google Scholar 

  180. US Patent 5654163, 1997.

  181. US Patent 4263426, 1981.

  182. Mukaiyama, T., Shintou, T., and Fukumoto, K., J. Am. Chem. Soc., 2003, vol. 125, no. 35, p. 10538.

    Article  CAS  PubMed  Google Scholar 

  183. Shintou, T., Fukumoto, K., and Mukaiyama, T., Bull. Chem. Soc. Jpn., 2004, vol. 77, no. 8, p. 1569.

    Article  CAS  Google Scholar 

  184. EP Patent 1436407, 2006.

  185. Tsutsumi, N., Ito, Y., and Sakai, W., Chem. Phys., 2008, vol. 344, nos. 1–2, p. 189.

    Article  CAS  Google Scholar 

  186. Hirao, T., Moriuchi, T., Ishikawa, T., Nishimura, K., Mikami, S., Ohshiro, Y., and Ikeda, I., J. Mol. Catal. A: Chem., 1996, vol. 113, nos. 1–2, p. 117.

    Article  CAS  Google Scholar 

  187. US Patent 3935247, 1976.

  188. JP Patent 75-93. 931, 1975.

  189. DE Patent 2221624, 1972.

  190. US Patent 3987068, 1976.

  191. Mostaghim, R. and Ahmadibeni, Y., Acta Chim. Slov., 2003, vol. 50, no. 3, p. 569.

    CAS  Google Scholar 

  192. Kolesnik, I.G., Zhizhina, E.G., and Matveev, K.I., J. Mol. Catal. A: Chem., 2000, vol. 153, nos. 1–2, p. 147.

    Article  CAS  Google Scholar 

  193. Kolesnik, I.G., Zhizhina, E.G., and Matveev, K.I., React. Kinet. Catal. Lett., 1999, vol. 68, no. 2, p. 339.

    Article  CAS  Google Scholar 

  194. Zhizhina, E.G., Simonova, M.V., Odyakov, V.F., and Matveev, K.I., Chem. Sust. Dev., 2004, vol.12, no. 6, p.663.

    Google Scholar 

  195. Oxidation and Reduction of Phenols. The Chemistry of the Hydroxyl Group. Part 1. Chap. 10, Patai, S., Ed., London: Wiley, 1971.

    Google Scholar 

  196. Rodikova, Yu.A., Zhizhina, E.G., and Pai, Z.P., Int. Research J., 2017, vol. 65, no. 11(4), p. 126.

  197. Rodikova, Yu.A., Zhizhina, E.G., and Pai, Z.P., Int. Research J., 2017, vol. 66, no. 12(4), p. 155.)

  198. Rodikova, Yu.A., Zhizhina, E.G., and Pai, Z.P., Appl. Catal., A, 2018, vol. 549, p. 216.

  199. Rodikova, Yu.A., Zhizhina, E.G., and Pai, Z.P., React. Kinet. Mech. Catal., 2018, vol. 124, p. 469.

    Article  CAS  Google Scholar 

  200. Rodikova, Yu.A., Zhizhina, E.G., and Pai, Z.P., Chem. Select., 2018, vol. 3, no. 16, p. 4200.

    CAS  Google Scholar 

  201. Ma, J., Wang, M., Du, Z., Chen, C., Gao, J., and Xu, J., Polym. Chem., 2012, vol. 3, p. 2346.

    Article  CAS  Google Scholar 

  202. van Putten, R.-J., van der Waal, J.C., de Jong, E., Rasrendra, C.B., Heeres, H.J., and de Vries, J.G., Chem. Rev., 2013, vol. 113, p. 1499.

    Article  CAS  PubMed  Google Scholar 

  203. Delidovich, I., Hausoul, P.J.C., Deng, L., Pfützenreuter, R., Rose, M., and Palkovits, R., Chem. Rev., 2016, vol. 116, p. 1540.

    Article  CAS  PubMed  Google Scholar 

  204. Nie, J.F. and Liu, H.C., Pure Appl. Chem., 2012, vol. 84, p. 765.

    Article  CAS  Google Scholar 

  205. Sádaba, I., Gorbanev, Y.Y., Kegnaes, S., Putluru, S.S.R., Berg, R.W., and Riisager, A., ChemCatChem, 2013, vol. 5, p. 284.

    Article  CAS  Google Scholar 

  206. Antonyraj, C.A., Jeong, J., Kim, B., Shin, S., Kim, S., Lee, K.-Y., and Cho, J.K., J. Ind. Eng. Chem., 2013, vol. 19, p. 1056.

    Article  CAS  Google Scholar 

  207. Rodikova, Yu.A. and Zhizhina, E.G., Chemistry under the sign of SIGMA: Research, Innovation, Technology. VI All-Russian Scientific Youth School-Conference (May 18-20, 2020, Omsk), Novosibirsk: IC SB RAS, 2020.

  208. Rodikova, Yu.A. and Zhizhina, E.G., React. Kinet. Mech. Catal., 2020, vol. 130, no. 1, p. 403.

    Article  CAS  Google Scholar 

  209. Zhizhina, E.G., Simonova, M.V., Russkikh, V.V., and Matveev, K.I., Katal. Prom-sti., 2005, no. 1, p. 12.

  210. Zhizhina, E.G. and Odyakov, V.F., ChemCatChem, 2012, vol. 4, p. 1405.

    Article  CAS  Google Scholar 

  211. Gogin, L. and Zhizhina, E., Mod. Res. Catal., 2013, vol. 2, p. 90.

    Article  CAS  Google Scholar 

  212. Gogin, L.L., Zhizhina, E.G., Pai, Z.P., and Parmon, V.N., Russ. Chem. Bull., 2015, vol. 64, no. 9, p. 2069.

    Article  CAS  Google Scholar 

  213. Gogin, L. and Zhizhina, E., Mod. Res. Catal., 2014, vol. 3, no. 2, p. 57.

    Google Scholar 

  214. Gogin, L.L. and Zhizhina, E.G., Katal. Prom-sti., 2014, vol. 6, no. 4, p. 273.

    Google Scholar 

  215. Gogin, L.L., Zhizhina, E.G., and Pai, Z.P., Kinet. Catal., 2019, vol. 60, no. 1, p. 75.

    Article  Google Scholar 

  216. Gogin, L.L., Zhizhina, E.G., and Pai, Z.P., Katal. Prom-sti., 2016, vol. 8, no. 4, p. 310.

    Google Scholar 

  217. Anthraquinone, in Kirk-Othmer Encyclopedia of Chemical Technology, 5th ed., 2006, vol. 2.

  218. Zhizhina, E.G., Matveev, K.I., and Russkikh, V.V., Chem. Sust. Dev., 2004, vol. 1, no. 1, p. 47.

    Google Scholar 

  219. Gogin, L.L., Zhizhina, E.G., and Pai, Z.P., Kinet. Catal., 2018, vol. 59, no. 5, p. 578.

    Article  CAS  Google Scholar 

  220. Gogin, L.L., Zhizhina, E.G., and Pai, Z.P., Mod. Res. Catal., 2019, vol. 8, p. 1.

    Article  CAS  Google Scholar 

  221. Simonova, M.V. and Zhizhina, E.G., Chem. Sust. Dev., 2005, vol. 13, no. 3, p. 477.

    Google Scholar 

  222. Gogin, L.L. and Zhizhina, E.G., Kinet. Catal., 2020, vol. 61, no. 2, p. 276.

    Article  CAS  Google Scholar 

  223. Gogin, L.L. and Zhizhina, E.G., Kinet. Catal., 2020, vol. 61, no. 4, p. 516.

    Article  CAS  Google Scholar 

  224. Gogin, L.L. and Zhizhina, E.G., Kinet. Catal., 2008, vol. 49, no. 6, p. 773.

    Article  CAS  Google Scholar 

  225. Zhizhina, E.G. and Odyakov, V.F., Int. J. Chem. Kinet., 2014, vol. 46, no. 9, p. 567.

    Article  CAS  Google Scholar 

Download references

Funding

This study was fulfilled within the framework of the budjet project of the Institute of Catalysis, Siberian Branch, Russian Academy of Sciences (no. АААА-А21-121011390007-7).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to L. L. Gogin.

Ethics declarations

The authors have no conflicts of interest to declare that are relevant to the contents of this article.

Additional information

Translated by L. Smolina

Abbreviations and notation: HPC, heteropoly compound; HPA, heteropolyacid; HPA-x, Мо−V−P heteropoly acid with x vanadium atoms; HPAn, heteropolyanion; Su, substrate; m, degree of reduction of the HPA-х solution; η, viscosity; ρ, density; χ, specific electric conductivity; SHE, standard hydrogen electrode; Е, redox potential; S, selectivity; OS, organic solvent; ∆rH, reaction enthalpy; ∆fH, formation enthalpy; MEK, methylethylketone; NMR, nuclear magnetic resonance; EPR, electron paramagnetic resonance; RS, Raman spectroscopy; MD, menadione, 2-methyl-1,4-naphthoquinone; TMP, trimethylphenol; TMBQ, trimethyl-1,4-benzoquinone; DAP, dialkylphenol; DABQ, dialkyl-1,4-benzoquinone; DMBQ, 2,6-dimethyl-1,4-benzoquinone; DTBQ, di-tert-butyl-1,4-benzoquinone; AQ, 9,10-anthraquinone; NQ, 1,4-naphthoquinone; DFF, 2,5-diformylfuran; HQ, hydroquinone; BQ, 1,4-benzoquinone; HH, hydrazine hydrate; 5-HMF, 5-hydroxymethylfurfurol; НОAc, acetic acid; LA, levulinic acid; FA, formic acid; MIBK, methylisobutylketone; THA, 1,4,4а,9а-tetrahydro-9,10-anthraquinone; DHA, 1,4-dihydro-9,10-anthraquinone; TMAQ, 2,3,6,7-tetramethylanthraquinone; DMB, 2,3-dimethylbutadiene; THNQ, substituted tetrahydro-1,4-naphthoquinone; DHNQ, substituted dihydro-1,4-naphthoquinone.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zhizhina, E.G., Gogin, L.L., Rodikova, Y.A. et al. Catalysts Based on High-Vanadium Solutions of Molybdovanadophosphoric Heteropolyacids: Achievements, Challenges, and Prospects. Kinet Catal 62, 197–232 (2021). https://doi.org/10.1134/S0023158421020129

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S0023158421020129

Keywords:

Navigation