Summary
The incorporation of starch hydrolysates in phenolic resins of the novolak and resol type via intermediate acid catalyzed dehydration to 5-hydroxymethylfurfural (HMF) has been investigated. The course of reaction was monitored by carbon-13-NMR and IR spectroscopy. Due to the formation of HMF/phenol condensates, savings of up to 40 % phenol and 50 % formaldehyde (by weight) are possible in comparison to commercial resins. Besides maintenance of essential property profiles, additional benefits may be achieved with respect to faster curing and lower amounts of free monomers.
Similar content being viewed by others
References
Chem. Ind. 35, 179 (1983)
J. Semel and R. Steiner, Chem. Ind. 35, 489 (1983)
H.U. Woelk, Nachr. Chem. Techn. Lab. 30, 204 (1982)
H.U. Woelk, Stärke/Starch 33, 397 (1981)
A. Budzinski, Chem. Ind. 34, 505 (1982)
J.P. Mudde, Mod. Plast. 57, 69 (1980)
J.P. Mudde, Pap. Synth. Conf. Proc. 1980, 113
H. Koch, F. Krause, R. Steffan, and H.U. Woelk, Stärke/Starch 35, 304 (1983)
US 4048126 and US 4048127 (CPC Intern.)
H.H. Szmant and D.D. Chundury, J. Chem. Techn. Biotechnol. 31, 135 (1981)
K. Bock and Chr. Pedersen, Adv. Carbohydr. Chem. Biochem. 41, 27 (1983)
A.H. Fawcett and W. Dadamba, Makromol. Chem. 183, 2799 (1982)
St. A. Sojka, R.A. Wolfe, E.A. Dietz jr., and B.F. Dannels, Macromolecules 12, 767 (1979).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Koch, H., Pein, J. Condensation reactions between phenol, formaldehyde and 5-hydroxymethylfurfural, formed as intermediate in the acid catalyzed dehydration of starchy products. Polymer Bulletin 13, 525–532 (1985). https://doi.org/10.1007/BF00263474
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00263474