Succinic or glutaric anhydride modified linear unsaturated (epoxy) polyesters

The influence of the structure of succinic or glutaric anhydride modified linear unsaturated (epoxy) polyesters on the course of the cure reaction with styrene initiated by benzoyl peroxide (BPO) or the mixture of benzoyl peroxide/tetrahydrophthalic anhydride (BPO/THPA) or benzoyl peroxide/maleic anhydride, as well as viscoelastic properties and thermal behavior of their styrene copolymers have been studied by DSC, DMA, and TGA analyses. Additionally, mechanical properties: flexural properties using three-point bending test and Brinell’s hardness for studied copolymers were evaluated. It was confirmed that the structure of used polyesters had a considerable influence on the course of the cure reaction with styrene, viscoelastic, thermal, and mechanical properties of prepared styrene copolymers. Generally, one or two asymmetrical peaks for the cure reaction of succinic or glutaric anhydride modified linear unsaturated epoxy polyesters with styrene were observed. They were connected with various cure reaction, e.g., copolymerization of carbon–carbon double bonds of polyester with styrene, thermal curing of epoxy groups, polyaddition reaction of epoxy to anhydride groups in dependence of used curing system. In addition, only one asymmetrical, exothermic peak attributed to the copolymerization process of succinic or glutaric anhydride modified linear unsaturated polyesters with styrene was visible. Moreover, the obtained styrene copolymers based on succinic or glutaric anhydride modified linear unsaturated epoxy polyesters were characterized by higher values of \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$ E_{{20\,^{\circ}{\text{C}}}}^{\prime} $$\end{document}, Tg, E″, νe, Emod, Fmax, hardness, IDT, FDT but lower ε − Fmax compared to those values observed for styrene copolymers prepared in the presence of succinic or glutaric anhydride modified linear unsaturated polyesters. This supported to the production of stiffer and more thermally stable polymeric structure of copolymers based on unsaturated epoxy polyesters. Moreover, the copolymers prepared in the use of glutaric anhydride modified linear unsaturated (epoxy) polyesters were described by lower values of \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$E_{{20\,^{\circ}{\text{C}}}}^{\prime} $$\end{document}, Tg, E″, νe, Emod, Fmax, hardness, IDT, FDT but higher ε − Fmax than those based on succinic anhydride modified linear unsaturated (epoxy) polyesters. The presence of longer aliphatic chain length in polyester’s structure leads to produce more flexible network structure of styrene copolymers based on glutaric anhydride modified linear unsaturated (epoxy) polyesters than those based on succinic anhydride modified linear unsaturated (epoxy) polyesters.