Some features of trichlorobiphenyls photolysis

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Resumo

The photolytic decomposition of the Trikhlorbifenil mixture, 2,4,5- and 2,4,6-trichlorobiphenyls under an influence of ultraviolet radiation in presence of tungsten oxide as a catalyst in a methanol medium was studied. A higher rate of photolysis of individual congeners of polychlorbiphenyls was established compared to the congeners of the Trikhlorbifenil mixture. The influence of structural features of polychlorarenes on a depth of photodecomposition and a routes of formation of photodestruction products was considered.

Sobre autores

T. Gorbunova

I.Ya. Postovskii Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences

Email: gorbunova@ios.uran.ru

M. Pervova

I.Ya. Postovskii Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences

G. Zakharova

Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences

N. Podval'naya

Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences

A. Enyashin

Institute of Solid State Chemistry, Ural Branch of the Russian Academy of Sciences

V. Saloutin

I.Ya. Postovskii Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences

O. Chupakhin

I.Ya. Postovskii Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences

Bibliografia

  1. Lin Y., Gupta G., Baker J. // Chemosphere. 1995. Vol. 31. P. 3323. doi: 10.1016/0045-6535(95)00177-A
  2. Reddy A.V.B., Moniruzzaman M., Aminabhavi T.M. // Chem. Eng. J. 2019. Vol. 358. P. 1186. doi: 10.1016/j.cej.2018.09.205
  3. Sinkkonen S., Paasivirta J. // Chemosphere. 2000. Vol. 40. P. 943. doi: 10.1016/S0045-6535(99)00337-9
  4. Czaplicka M. // J. Hazard. Mater. (B). 2006. Vol. 134. P. 45. doi: 10.1016/j.jhazmat.2005.10.039
  5. Xing Z., Zhang J., Cui J., Yin J., Zhao T., Kuang J., Xiu Z., Wan N., Zhou W. // Appl. Catal. (B). 2018. Vol. 225. P. 452. doi: 10.1016/j.apcatb.2017.12.005
  6. Исаева Е.И., Гурьев Н.В., Бойцова Т.Б., Пронин В.П., Старицын М.В., Федосеев М.Л. // ЖОХ. 2022. Т. 92. Вып. 10. С. 1603
  7. Isaeva E.I., Gur'ev N.V., Boitsova T.B., Pronin V.P., Staritsyn M.V., Fedoseev M.L. // Russ. J. Gen. Chem. 2022. Vol. 92. N 10. P. 1972. doi: 10.1134/S1070363222100115
  8. Langford C.H., Achari G., Izadifard M. // J. Photochem. Photobiol. (A). 2011. Vol. 222. P. 40. doi: 10.1016/j.jphotochem.2011.04.028
  9. Huang L., Dong W., Hou H. // J. Photochem. Photobiol. (A). 2013. Vol. 268. P. 44. doi: 10.1016/j.jphotochem.2013.06.016
  10. Miao X.S., Chu S.G., Xu X.B. // Chemosphere. 1999. Vol. 39. P. 1639. doi: 10.1016/S0045-6535(99)00062-4
  11. Chang F.C., Chiu T.C., Yen J.H., Wang Y.S. // Chemosphere. 2003. Vol. 51. P. 775. doi: 10.1016/S0045-6535(03)00003-1
  12. Yao Y., Kakimoto K., Ogawa H.I., Kato Y, Hanada Y., Shinohara R., Yoshino E. // Chemosphere. 1997. Vol. 35. P. 2891. doi: 10.1016/S0045-6535(97)00282-8
  13. Yao Y., Kakimoto K., Ogawa H.I., Kato Y, Kadokami K., Shinohara R. // Chemosphere. 2000. Vol. 40. P. 951. doi: 10.1016/S0045-6535(99)00338-0
  14. Manzano M.A., Perales J.A., Sales D., Quiroga J.M. // Chemosphere. 2004. Vol. 57. P. 645. doi: 10.1016/j.chemosphere.2004.07.014
  15. De Felip E., Ferri F., Lupi C., Trieff N.M., Volpi F., di Domenico A. // Chemosphere. 1996. Vol. 33. P. 2263. doi: 10.1016/0045-6535(96)00333-5
  16. Tang T., Zheng Z., Wang R., Huang K., Li H., Tao X., Dang Z., Yin H., Lu G. // Chemosphere. 2018. Vol. 193. P. 861. doi: 10.1016/j.chemosphere.2017.11.095
  17. Gorbunova T.I., Kozhevnikova N.S., Vorokh A.S., Enyashin A.N., Pervova M.G., Zapevalov A.Ya., Saloutin V.I., Chupakhin O.N. // Reac. Kinet. Mech. Cat. 2019. Vol. 126. P. 1115. doi: 10.1007/s11144-019-01543-7
  18. Zakharova G.S., Podval'naya N.V., Gorbunova T.I., Pervova M.G., Murzakaev A.M., Enyashin A.N. // J. Alloys Compd. 2023. Vol. 938. 168620. doi: 10.1016/j.jallcom.2022.168620
  19. Первова М.Г., Горбунова Т.И., Плотникова К.А., Салоутин В.И., Чупахин О.Н. // ЖОХ. 2015. Т. 85. Вып. 8. С. 1374
  20. Pervova M.G., Gorbunova T.I., Plotnikova K.A., Saloutin V.I., Chupakhin O.N. // Russ. J. Gen. Chem. 2015. Vol. 85. N 8. P. 1929. doi: 10.1134/S1070363215080216
  21. Mills III S.A., Thal D.I., Barney J. // Chemosphere. 2007. Vol. 68. P. 1603. doi: 10.1016/j.chemosphere200703052
  22. Mullin M.D., Pochini C.M., McGrindle M.R., Romkes M., Safe S.H., Safe L.M. // Environ. Sci. Technol. 1984. Vol. 18. P. 468.
  23. Занавескин Л.Н., Аверьянов В.А. // Усп. хим. 1998. Т. 67. № 8. С. 788
  24. Zanaveskin L.N., Averyanov V.A. // Russ. Chem. Rev. 1998. Vol. 67. N 8. P. 713. doi: 10.1070/RC1998v067n08ABEH000412
  25. Li Q., Chen Z., Wang H., Yang H., Wen T., Wang S., Hu B., Wang X. // Sci. Total. Environ. 2021. Vol. 792. 148546. doi: 10.1016/j.scitotenv.2021.148546
  26. Islam M.N., Park J.-H., Shin M.-S., Park H.-S. // Chemosphere. 2014. Vol. 109. P. 28. doi: 10.1016/j.chemosphere.2014.02.057

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