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Catalytic transformations of m-xylene in presence of aluminum silicates

  • Organic and Biological Chemistry
  • Published:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    A study was made of the conditions required for the isomerization of m-xylene in presence of gumbrin and of a synthetic aluminum silicate catalyst at different temperatures and pressures.

  2. 2.

    In presence of gumbrin the isomerization of m-xylene proceeds most smoothly at 450‡ under atmospheric pressure and at a space velocity of 0.5 hour−1. Under these conditions the yield of p-xylene attains 91.2% of the equilibrium amount.

  3. 3.

    The use of reduced pressure (50 mm) favors the complete elimination of undesirable methylation and demethylation reactions and makes it possible to obtain almost 100% of liquid catalyzate containing 15.6% of p-xylene. The use of hydrogen under pressure (15 atm) results in the complication of the isomerization reaction by side reactions.

  4. 4.

    The synthetic aluminum silicate was a less effective catalyst than gumbrin in that it favored side reactions and gas formation to a greater extent.

  5. 5.

    In presence of Pt-Al2O3 at 500‡, m-xylene was again isomerized into the o- and p-isomers, but simultaneous formation of toluene (up to 5.5%) and trimethylbenzenes (up to 2.5%) occurred.

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Literature cited

  1. E. R. Boedeker and W. E. Erner, J. Amer. Chem. Soc. 76, 3591 (1954).

    Google Scholar 

  2. A. D. Sulimov, V. I. Karzhev, T. V. Zhokhovskaia, V. M. Olevskii, E. G. Vebdel'shtein, E. I. Sil'chenko, N. V. Shavolian, and A. A. Voitekhov, Chemistry and Technology of Fuel, No. 1, 33 (1956).

    Google Scholar 

  3. Iu. G. Mamedaliev, A. V. Topchiev and G. M. Mamedaliev, Proc. Acad. Sci. USSR, 106, 1027 (1956).

    Google Scholar 

  4. P. M. Pitts, J. E. Connor and L. W. Leum, Industr. and Engng. Chem. 47, 770 (1955).

    Google Scholar 

  5. U. S. Patent 2632779 3/24/1953;Chem Abstrs. 48, 2096 (1954); U. S. Patent 2656397, 10/20/1953; Referat. Zh. Khim. No. 23, 258 (1954); U. S. Patent 2695323, 11/23/1954; Referat. Zh. Khim. No 23. 396 (1955); British Patent 695947, 8/19/1953; Chem. Abstrs. 48,8821 (1954); French Patent 1082941, 6/22/1953; Chem. Zentr-alblatt 42, 11598 (1956).

  6. H. W. Haines, J. M. Powers and R. B. Bennet, Industr. and Engng. Chem. 47, 1096 (1955).

    Google Scholar 

  7. J. Mlodecka, Przem. Chem. 11, 315 (1955); Referat. Zh. Khim. No.7, 264 (1956).

    Google Scholar 

  8. W. J. Taylor, D. D. Wagman, M. G. Williams, K. S. Pitzer, and F. D. Rossini, J. Res. Nat. Bur. Standards 37, 95 (1946).

    Google Scholar 

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Shuikin, N.I., Tulupova, E.D. & Poliakova, Z.P. Catalytic transformations of m-xylene in presence of aluminum silicates. Russ Chem Bull 7, 1422–1426 (1958). https://doi.org/10.1007/BF00914856

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  • DOI: https://doi.org/10.1007/BF00914856

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