Patel M P, Braden M, Davy K W
Biomaterials. 1987 Jan;8(1):53-6. doi: 10.1016/0142-9612(87)90030-5.
The polymerization shrinkage of a range of poly(n-alkyl methacrylates) in the range C1 to C16, some of their isomers and the polymers of cyclic and heterocyclic methacrylates have been measured using densitometry. The percentage volume shrinkage decreases with the size of the substituent side group. This proved to reflect the fact that the change in molar volume on polymerizing a methacrylate ester is reasonably constant at 22 cc/mol irrespective of the geometry of the substituent group. However, the glass transition temperature of the polymer depends very critically on the geometry of the side group. Hence one method for the development of low shrinkage glassy polymers is to investigate methacrylate esters of large molar volume, but with side group geometry that results in a high glass transition temperature. Polymerization shrinkage can be used to determine the degree of conversion of a polymer, using the value of 22 cc/mol as the change in molar volume.
已使用密度测定法测量了一系列碳原子数在C1至C16范围内的聚甲基丙烯酸正烷基酯、它们的一些异构体以及环状和杂环甲基丙烯酸酯聚合物的聚合收缩率。体积收缩百分比随取代基侧基尺寸的增大而减小。这证明反映了一个事实,即甲基丙烯酸酯聚合时摩尔体积的变化在22立方厘米/摩尔左右基本恒定,与取代基的几何形状无关。然而,聚合物的玻璃化转变温度非常关键地取决于侧基的几何形状。因此,开发低收缩率玻璃态聚合物的一种方法是研究大摩尔体积的甲基丙烯酸酯,但侧基几何形状要能导致高玻璃化转变温度。利用22立方厘米/摩尔作为摩尔体积变化值,聚合收缩率可用于确定聚合物的转化率。