Howard M. Relles
General Electric
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Polymer science and technology | 1984
Frank J. Williams; A. S. Hay; Howard M. Relles; J. C. Carnahan; G. R. Loucks; B. M. Boulette; P. E. Donahue; D. S. Johnson
The synthesis of aliphatic polyformals (1) has been known for many years and is relatively straightforwardl. As shown in equation 1, aliphatic diols can be reacted directly with formaldehyde or dialkyl formals (2) to produce these polymers. The principal complication of the reaction occurs when the diol used contains 2, 3 or 4 carbon atoms in which case the formation of the cyclic formal (3) is favored.
Journal of Polymer Science Part A | 1981
Dwain M. White; T. Takekoshi; F. J. Williams; Howard M. Relles; P. E. Donahue; Howard J. Klopfer; G. R. Loucks; J. S. Manello; R. O. Matthews; R. W. Schluenz
Archive | 1976
Howard M. Relles; Donald Scott Johnson
Archive | 1980
Frank J. Williams; Howard M. Relles
Archive | 1975
Donald Scott Johnson; Howard M. Relles
Journal of Polymer Science: Polymer Letters Edition | 1983
A. S. Hay; Frank J. Williams; Howard M. Relles; B. M. Boulette; P. E. Donahue; D. S. Johnson
Journal of Organic Chemistry | 1977
Frank J. Williams; Howard M. Relles; J. S. Manello; P. E. Donahue
Journal of Organic Chemistry | 1977
Frank J. Williams; Howard M. Relles; P. E. Donahue; J. S. Manello
Journal of Polymer Science Part A | 1977
Howard M. Relles; Charles M. Orlando; D. R. Heath; R. W. Schluenz; J. S. Manello; S. Hoff
Journal of Polymer Science Part A | 1973
Howard M. Relles; R. W. Schluenz