Examination of the reaction of a macromolecular sulfonamide with sodium nitrite in acidic media

R. Bogoczek; E. Kociołek-Balawejder; E. Stanisławska

Published : 2022-08-26

Vol. 52 No. 2 (2007)

Examination of the reaction of a macromolecular sulfonamide with sodium nitrite in acidic media

R. Bogoczek E. Kociołek-Balawejder E. Stanisławska

Abstract

In this study we have examined the reaction of macromolecular sulfonamide (styrene/divinylbenzene copolymer with the macroporous structure containing -SO2NH2 groups) with nitrites in acidic media. We found that the lowest admissible pH of the reaction medium providing the stability of the functional groups was 4.0. The lower the pH, the quicker the functional group lost its nitrogen atom and transformed to a sulfonic group. Knowledge of the chemical stability of sulfonamide groups in the presence of nitrites is not only of cognitive but also of practical value, because N-chloro derivatives of a sulfonamide copolymer (containing so-called active chlorine) are useful for the elimination of nitrites from waters through their oxidation to less toxic nitrates.

Keywords

wielkocząsteczkowy sulfonamid ; kopolimer styren-diwinylobenzen ; destrukcja grup sulfonamidowych ; reakcja sulfonamidu z azotynem macromolecular sulfonamide ; styrene/divinylbenzene copolymer containing sulfonamide functional groups ; destruction of sulfonamide groups ; reaction of sulfonamide with nitrite

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Bogoczek, R., Kociołek-Balawejder, E., & Stanisławska, E. (2022). Examination of the reaction of a macromolecular sulfonamide with sodium nitrite in acidic media. Polimery, 52(2), 137–141. Retrieved from https://ichp.vot.pl/index.php/p/article/view/1401

References

Emerson D. W.: Ind. Eng. Chem. Prod. Res. Dev. 1978, 17, 270.

2. Emerson D. W.: Ind. Eng. Chem. Res. 1988, 27, 1797.

3. Emerson D. W., Ifalade S. O.: Ind. Eng. Chem. Res. 2005, 44, 7045.

4. Salunkhe M. M, Mane R. B., Kanade A. S.: Eur. Polym. J. 1991, 27, 461.

5. Kociołek-Balawejder E.: Eur. Polym. J. 2000, 36, 295.

6. Kociołek-Balawejder E.: Eur. Polym. J. 2000, 36, 1137.

7. Zhang Y., Emerson D. W., Steinberg S. M.: Ind. Eng. Chem. Res. 2003, 42, 5959.

8. Kociołek-Balawejder E.: React. Funct. Polym. 1999, 41, 227.

9. Kociołek-Balawejder E.: Eur. Polym. J. 2002, 38, 953.

10. Kociołek-Balawejder E.: React. Funct. Polym. 2002, 52, 89.

11. Bogoczek R., Kociołek-Balawejder E., Stanisławska E.: Ind. Eng. Chem. Res. 2005, 44, 8530.

12. Bogoczek R., Kociołek-Balawejder E., Stanisławska E.: React. Funct. Polym. 2006, 66, 609.

13. Smith P.: “The Chemistry of Open-Chain Organic Nitrogen Compounds”, vol. I, W. A. Benjamin, Inc., New York 1965.

14. Bogoczek R., Kociołek-Balawejder E.: Polymer Comm. 1986, 27, 286.

15. Williams W. J.: “Handbook of Anion Determination”, Butterworth, London 1979.

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R. Bogoczek bogorom@credit.ae.wroc.pl

Affiliation
Wrocław University of Economics, Department of Industrial Chemistry, 53-345 Wroclaw, Poland

E. Kociołek-Balawejder

E. Stanisławska