详细信息

Preparation of Nonlinear Structure Poly(glycolic acid) with High Toughness, Excellent Hydrolysis Stability, and Foaming Performance  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Preparation of Nonlinear Structure Poly(glycolic acid) with High Toughness, Excellent Hydrolysis Stability, and Foaming Performance

作者:Chen, Shiyuan[1];Meng, Xin[1];Xin, Zhong[1];Gong, Weiguang[2];Li, Chenyang[1];Wen, Wei[1]

机构:[1]East China Univ Sci & Technol, Sch Chem Engn, Mat Chem Engn & Prod Engn Dept, Shanghai Key Lab Multiphase, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Res & Dev Ctr Sports Mat, Shanghai 200237, Peoples R China

年份:2024

卷号:63

期号:20

起止页码:9058

外文期刊名:INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH

收录:;EI(收录号:20242016087496);WOS:【SCI-EXPANDED(收录号:WOS:001225231200001)】;

基金:This work was supported by JH Material Scientific Co., Ltd., China.

语种:英文

外文关键词:Acrylic monomers - Grafting (chemical) - Impact strength - Tensile strength

摘要:Poor toughness and fast hydrolysis degradation are the key barriers for poly(glycolic acid) (PGA) toward broader applications. Herein, nonlinear structure PGA with high toughness and excellent hydrolysis stability was prepared through graft and chain extending reaction in the presence of bis(tert-butylperoxyisopropyl)benzene (BIPB) and glycidyl methacrylate (GMA). The rheological behavior, the gel content, and the GPC result demonstrated that GMA was grafted onto PGA chains, and then the epoxy group of grafted GMA reacted with the end groups of PGA, which resulted in the formation of a nonlinear structure in which one original PGA chain connected to the other PGA backbone. The PGA/1.0BIPB/1.0GMA which had the highest nonlinear degree was obtained when the amounts of BIPB and GMA were all 1.0 wt % with respect to PGA, and it showed some excellent characterization. Compared to that of virgin PGA, the elongation at break and impact strength of PGA/1.0BIPB/1.0GMA increased by 547 and 18%, respectively. Moreover, PGA/1.0BIPB/1.0GMA also possessed a faster crystallization rate. The hydrolysis results showed that the tensile strength of PGA/1.0BIPB/1.0GMA decreased by half on the 12th day, delaying by 7 days compared with that of virgin PGA. Furthermore, PGA/1.0BIPB/1.0GMA also had better foaming ability of a 24.68-fold volume expansion ratio. Thus, this work paved a new strategy to design nonlinear structure PGA with high toughness, excellent hydrolysis stability, and ultrahigh foamability.

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