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The oxyethylation of dinonylphenol

  • Technical
  • Published:
Journal of the American Oil Chemists Society

Abstract

Countercurrent extraction data have shown that ethylene oxide adducts of dinonylphenol have a wider molecular-weight distribution than is predicted by the Flory-Poisson calculation. The difference is attributed to the fact that the dinonylphenol is not completely converted to dinonylphenoxyethanol before subsequent monomer additions occur.

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Authors and Affiliations

  1. Research Laboratories, The Rohm and Haas Company, Bristol, Pennsylvania

    R. C. Mansfield, J. E. Locke & K. A. Booman

Authors
  1. R. C. Mansfield
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  2. J. E. Locke
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  3. K. A. Booman
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Cite this article

Mansfield, R.C., Locke, J.E. & Booman, K.A. The oxyethylation of dinonylphenol. J Am Oil Chem Soc 38, 289–291 (1961). https://doi.org/10.1007/BF02638429

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  • DOI: https://doi.org/10.1007/BF02638429

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