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38. 39. 40. 41. 42. 43. 44. 45. 46. 47. 48. 49. 50. 51. 52. 53. 54. 55. 56. 57. 58. 59. 60. 61. 62. 63. 64. , Polymer (1997) 38(4), p. , Polymer (1997) 38(4), p. , Polymer (1997) 38(4), p. , Makromol. -Rapid Commun. (1986) 7, p. , Macromolecules (1987) 20, p. , Ring Opening Polymerization. , eds. , Ring Opening Polymerization. , eds. , Ring Opening Polymerization. , eds. , Ring Opening Polymerization. , eds. , Kogyo Kagaku Zasshi (1962) 65, p. , Kogyo Kagaku Zasshi (1962) 65, p. , Kogyo Kagaku Zasshi (1962) 65, p.

By organic chemistry formalism, polyacetals are reaction products of aldehydes with polyhydric alcohols. Polymers generated from aldehydes, however, either via cationic or anionic polymerization are generally known as polyacetals because of repeating acetal linkages. , trioxane [29-30] (Fig. 5). Polyacetals are prone to degrade to the monomers at elevated temperatures by an unzipping mechanism. They are either end-capped or copolymerized with low levels of an alkylene oxide to prevent unzipping and impart better processability.

Makromol. Chem. (1969) 126, p. , Angew. Makromol. Chem. (1979) 75, p. , Makromol. Chem. (1979) 180, p. , Zesz. Nauk. Politech. , Chem. (1976) 32, p. 136 [Chem. Abstr. (1977) 86, p. S. S. , Angew. Makromol. Chem. (1977) 63, p. , Europ. Polym. J. (1972) 8, p. , Lactam-Based Polyamides. , Kubanek, V, eds.

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