The Effect of Functionalized SEBS on the Properties of PP/SEBS Blends

Author:

Song Lixin12ORCID,Cong Fei12,Wang Wei3,Ren Jiannan4,Chi Weihan12,Yang Bing12,Zhang Qian12,Li Yongchao12,Li Xianliang12,Wang Yuanxia12ORCID

Affiliation:

1. Polymer High Functional Film Engineering Research Center of Liaoning Province, Shenyang University of Chemical Technology, Shenyang 110142, China

2. College of Materials Science and Engineering, Shenyang University of Chemical Technology, Shenyang 110142, China

3. BatteroTech Co., Ltd., Shanghai 201417, China

4. AVIC Shenyang Aircraft Corporation, Shenyang 110850, China

Abstract

Styrene (St) was used as comonomer and glycidyl methacrylate (GMA) as grafting monomer to prepare SEBS-g-(GMA-co-St) graft copolymers via melt grafting. Then, the graft copolymers were employed as a compatibilizer for melt blending polypropylene (PP) and hydrogenated styrene-butadiene-styrene (SEBS) triblock copolymers. The effects of the amount of GMA in the graft copolymers on thermal properties, rheology, crystallization, optical and mechanical properties, and microstructure of the blends were investigated. The results show that GMA and St were successfully grafted onto SEBS. The GMA amount in the graft copolymer significantly influenced the comprehensive properties of PP/SEBS/SEBS-g-(GMA-co-St) blends. The epoxy groups of GMA reacted with PP and SEBS, forming interfacial chemical bonds, thereby enhancing the compatibility between PP and SEBS to varying extents. After introducing SEBS-g-(GMA-co-St) into PP/SEBS blends, crystallinity decreased, crystal size increased while transmittance remained above 91% with rising GMA amount in the graft copolymers, indicating excellent optical properties. Notched impact strength and elongation at break of the blends showed a trend of first increasing and then decreasing with increased amounts of GMA in the graft copolymers. When the amount of GMA in the graft copolymers was 3 wt%, the blends exhibited optimal toughness with notched impact strength and elongation at break of 30,165.82 J/m2 and 1445.40%, respectively. This was attributed to the tightest dispersion interface adhesion and maximum matrix plastic deformation, consistent with the mechanical performance results.

Funder

Foundation of Department of Education of Liaoning Province

Foundation of Liaoning Province Department of Education

Publisher

MDPI AG

Subject

Polymers and Plastics,General Chemistry

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