Ruyter I E
Acta Odontol Scand. 1981;39(1):27-32. doi: 10.3109/00016358109162255.
Oxygen inhibits radical polymerization, and for the present investigation, the thickness of the resulting unpolymerized surface layer on various proprietary dental polymers was measured by a microscopic technique. The inhibition depth of the polymerized resins varied from 7 to 84 micrometers. Resin systems with the tertiary aromatic amine 3,4-xylyl-diethanolamine as the activator had a thinner unpolymerized layer than those with p-tolyldiethanolamine. Increased viscosity also resulted in reduced thickness of the unpolymerized films. UV-light cured resins had thinner inhibited layers than those of comparable viscosity with a peroxide-amine initiator system. However, the thinnest unpolymerized film was seen with a chemically activated resin system containing acetone. This investigation has shown that the thickness of the unpolymerized film on cured dental resins is related to the composition and the initiating system.
氧气会抑制自由基聚合反应,在本研究中,通过一种显微技术测量了各种专利牙科聚合物上所得未聚合表面层的厚度。聚合树脂的抑制深度在7至84微米之间变化。以叔芳胺3,4-二甲苯基二乙醇胺作为活化剂的树脂体系,其未聚合层比以对甲苯基二乙醇胺的树脂体系更薄。粘度增加也会导致未聚合薄膜的厚度减小。紫外光固化树脂的抑制层比具有过氧化物-胺引发体系且粘度相当的树脂更薄。然而,在含有丙酮的化学活化树脂体系中观察到最薄的未聚合薄膜。本研究表明,固化牙科树脂上未聚合薄膜的厚度与组成和引发体系有关。