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Modification of poly(D,L-lactic acid)-co-poly(ethylene glycol) copolymer by low energy electron beam (EB) radiation

机译:低能电子束(EB)辐射对聚(D,L-乳酸)-共聚(乙二醇)共聚物的改性

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Poly(D,L-lactic acid)-co-poly(ethylene glycol) copolymer (D,L-PLEG) synthesized by melt polycondensation was irradiated using low energy electron beam (EB) in the presence of triallyl cyanurate (TAC) and tetraallyl pentaerythritol (TAPE) as crosslinking agents. The tensile strength of D,L-PLEG/TAC and D,L-PLEG/TAPE samples increases up to 48 MPa and 28 MPa at dose of 80 kGy and 60 kGy, respectively, and decreases with further increase of dose, whereas the elongation at break decreases continuously with increasing dose. The glass transition temperature (Tg) is improved to some extent due to the formation of molecular chain network. Degradation of D,L-PLEG is retarded with introduction of cross-linked network. The results suggest that the physical properties of crosslinked D,L-PLEG can be adjusted easily by varying irradiation dose.
机译:在三烯丙基氰尿酸酯(TAC)和四烯丙基的存在下,使用低能电子束(EB)照射通过熔融缩聚合成的聚(D,L-乳酸)-共聚(乙二醇)共聚物(D,L-PLEG)。季戊四醇(TAPE)作为交联剂。在剂量为80 kGy和60 kGy时,D,L-PLEG / TAC和D,L-PLEG / TAPE样品的抗张强度分别增加至48 MPa和28 MPa,并随着剂量的进一步增加而降低,而伸长率则降低断裂剂量随着剂量的增加而连续降低。由于分子链网络的形成,玻璃化转变温度(Tg)有所提高。随着交联网络的引入,D,L-PLEG的降解受到抑制。结果表明,可以通过改变照射剂量容易地调节交联的D,L-PLEG的物理性质。

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