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Heterogeneous styrene–divinylbenzene copolymers. Stability conditions of the porous structures

机译:非均相苯乙烯-二乙烯基苯共聚物。多孔结构的稳定性条件

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AbstractThe change in the porosity of styrene–divinylbenzene (S–DVB) copolymers during drying as a function of the quality of the diluent and of the divinylbenzene (DVB) concentration was investigated after drying the networks from water (maximum porosity) and from toluene (stable porosity). Two different diluents, namely toluene and cyclohexanol, were used in the polymerization system at a fixed volume fraction of the organic phase (0.50). The phase separation in toluene is accompanied by a slight deswelling of the network phase, whereas that in cyclohexanol leads to largely unswollen network phase. The stable porosity increases abruptly over a narrow range of the DVB concentration, i.e., between 40 and 50 DVB in toluene and between 15 and 25 DVE in cyclohexanol. The maximum porosity increases almost linearly with increasing DVB concentration up to a certain value, and then remains constant. The results indicate that the two main factors which determine the physical state of the swollen heterogeneous S–DVB copolymers, as well as the stability of the porous structures, are (1) the critical conversion at the incipient phase separation and (2) the degree of the inhomogeneity in crosslink distrib
机译:摘要研究了苯乙烯-二乙烯基苯(S-DVB)共聚物在干燥过程中孔隙率随稀释剂质量和二乙烯基苯(DVB)浓度的变化,研究了水(最大孔隙率)和甲苯(稳定孔隙率)干燥网络后的变化。在聚合体系中使用了两种不同的稀释剂,即甲苯和环己醇,有机相的固定体积分数(0.50)。甲苯中的相分离伴随着网相的轻微溶胀,而环己醇中的相分离导致网相基本未膨胀。稳定的孔隙率在DVB浓度的狭窄范围内突然增加,即甲苯中的DVB在40%至50%之间,环己醇中的DVE在15%至25%之间。最大孔隙率几乎随着DVB浓度的增加而线性增加,达到一定值,然后保持不变。结果表明,决定膨胀非均相S-DVB共聚物物理状态以及多孔结构稳定性的两个主要因素是(1)初期相分离时的临界转化率和(2)交联分布中的不均匀程度

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