Skip to main content
Log in

Continuous hydrogenation of fats and fatty acids at short contact times1

  • Published:
Journal of the American Oil Chemists’ Society

Abstract

Continuous hydrogenation of fats and fatty acids using suspended catalysts was studied in a vertical flow reactor packed with Raschig rings. A short time of reactive contact of the fat or the fatty acid with the catalyst and hydrogen is the unique feature of this system. A nickel catalyst used in the hydrogenation of soybean oil gave a reduction of 40-50 iodine value units per min, small amounts oftrans-isorners (10-20%), large proportions of linoleate in unreduced octadecadienoyl moieties (70-80%), and nonselective reduction of polyunsaturated acyl moieties (linoleate selectivity ratio 1-3). Another nickel catalyst, used in the hydrogenation of tallow fatty acids, also gave a reduction of 40-50 iodine value units per min and nonselective reduction of polyunsaturated fatty acids. A copper chromite catalyst used in the hydrogenation of soybean oil gave a reduction of 10-15 iodine value units per min, low levels oftrans- isomers (10-15%), and selective reduction of linolenoyl moieties (linolenate selectivity ratio 4-6). Composition of positional isomers of cis- andtrans-octadecenoyl moieties in partially hydrogenated products obtained both with nickel and copper chromite catalysts reveals that essentially the same mechanisms of isomerization are involved in continuous hydrogenation at short time of reactive contact as in batch hydrogenation.

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.

Similar content being viewed by others

References

  1. Albright, L.F., JAOCS 50:25S (1973).

    Google Scholar 

  2. Frankel, E.N., and H.J. Dutton, “Topics in Lipid Chemistry,” F.D. Gunstone, ed., Vol. l,Logos Press Limited, 1970.

  3. Kaufmann, H.P., and K.D. Mukherjee, Fette Seifen Anstrichm 67:606 (1965).

    Article  CAS  Google Scholar 

  4. Mukherjee, K.D., and I. Kiewitt, Chem. Ing. Tech. 45:475 (1973).

    Article  CAS  Google Scholar 

  5. Mukherjee, K.D., I. Kiewitt, and M. Kiewitt, JAOCS 52:282 (1975).

    Article  CAS  Google Scholar 

  6. Chalvardjian, A., Biochem. J. 90:518 (1964).

    CAS  Google Scholar 

  7. “DGF-Einheitsmethoden,” Wissenschaftliche Verlagsgesellschaft mbH, Stuttgart, Germany, C-IV 6, 1968.

  8. AOCS, “Official and Tentative Methods of the American Oil Chemistis’ Society,” AOCS, Champaign, IL, Method Cd 14-61 1964 (Revised to 1972).

    Google Scholar 

  9. Hamberg, M., and B. Samuelsson, J. Biol. Chem. 242:5329 (1967).

    CAS  Google Scholar 

  10. Morris, L.J., J. Lipid Res. 7:717 (1966).

    CAS  Google Scholar 

  11. Beroza, M., and B.A. Bierl, Anal. Chem. 39:1131 (1967).

    Article  CAS  Google Scholar 

  12. Johnston, A.E., and H.J. Dutton, JAOCS 49:98 (1972).

    Article  CAS  Google Scholar 

  13. Kleiman, R., G.F. Spencer, F.R. Earle, and I.A. Wolff, Lipids 4:135 (1969).

    Article  CAS  Google Scholar 

  14. Albright, L.F., JAOCS 40:16 (1963).

    Article  CAS  Google Scholar 

  15. Schmidt, H.J., Ibid. 45:520 (1968).

    Article  CAS  Google Scholar 

  16. Lefe’bvre, J., and J. Baltes, Fette Seifen Anstrichm. 77:125 (1975).

    Article  CAS  Google Scholar 

  17. Koritala, S., E. Selke, and H.J. Dutton, JAOCS 50:310 (1973).

    Article  CAS  Google Scholar 

  18. Scholfield, C.R.,Ibid. 49:583 (1972).

    Article  CAS  Google Scholar 

  19. Allen, R.R., and A.A. Kiess, Ibid. 32:400 (1955).

    Article  CAS  Google Scholar 

  20. Coenen, J.W.E., and H. Boerma, Fette Seifen Anstrichm. 70:8 (1968).

    Article  CAS  Google Scholar 

  21. Mounts, T.L., and H.J. Dutton, JAOCS 44:67 (1967).

    Article  CAS  Google Scholar 

  22. Ilsemann, K., I. Reichwald, and K.D. Mukherjee, Fette Seifen Anstrichm. 78:181 (1976).

    Article  CAS  Google Scholar 

  23. Koritala, S., R.O. Butterfield, and H.J. Dutton, JAOCS 50:317 (1973).

    Article  CAS  Google Scholar 

  24. Koritala, S., and H.J. Dutton, Ibid. 46:245 (1969).

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

1The terms “linoloyl” and “linolenoyl” are used throughout to designate9-cis, 12-cis-octadecadienoyl and 9-cis, 12-cis, 15-cis- octadecatrienoyl groups, respectively.

About this article

Cite this article

Ilsemann, K., Mukherjee, K.D. Continuous hydrogenation of fats and fatty acids at short contact times1. J Am Oil Chem Soc 55, 892–896 (1978). https://doi.org/10.1007/BF02671414

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02671414

Keywords

Navigation