Enhanced Poly(propylene carbonate) with Thermoplastic Networks: A Cross-Linking Role of Maleic Anhydride Oligomer in CO2/PO Copolymerization

被引:14
|
作者
Gao, Lijun [1 ]
Huang, Meiying [1 ,2 ]
Wu, Qifeng [1 ]
Wan, Xiaodan [1 ]
Chen, Xiaodi [1 ]
Wei, Xinxin [1 ]
Yang, Wenjing [1 ]
Deng, Rule [1 ]
Wang, Lingyun [2 ]
Feng, Jiuying [1 ]
机构
[1] Lingnan Normal Univ, Resource & Chem Engn Technol Res Ctr Western Guan, Sch Chem & Chem Engn, Key Lab Clean Energy Mat Chem Guangdong Higher Ed, Zhanjiang 524048, Peoples R China
[2] South China Univ Technol, Sch Chem & Chem Engn, Key Lab Funct Mol Engn Guangdong Prov, Guangzhou 510641, Guangdong, Peoples R China
基金
星火计划;
关键词
poly(propylene carbonate); networks; maleic anhydride oligomer; terpolymerization; ONE-STEP STRATEGY; RING-OPENING COPOLYMERIZATION; PROPYLENE-OXIDE; ALTERNATING COPOLYMERIZATION; ALIPHATIC POLYCARBONATES; DIOXIDE; EPOXIDES; TERPOLYMERIZATION; CATALYSTS; PLASTICS;
D O I
10.3390/polym11091467
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Cross-linking is an effective way to enhance biodegradable poly(propylene carbonate) (PPC) from CO2 and propylene oxide (PO). Cross-linked PPC can be prepared by one-step terpolymerization of multifunctional third monomers with CO2 and PO. However, few such third monomers are available. Each molecule of maleic anhydride oligomer (MAO) contains more than two cyclic anhydride groups. Here, we use it to synthesize PPC with cross-linked networks by adding a small quantity of MAO (0.625-5 wt% of PO) in CO2/PO copolymerization that was catalyzed by zinc glutarate. The formation of networks in the prepared copolymers was confirmed by the presence of gel in copolymers combined Fourier transform infrared spectroscopy (FT-IR), H-1 NMR, and the improved mechanical properties. The 5% weight-loss degradation temperatures and maximum weight-loss degradation temperatures greatly increase up to 289.8 degrees C and 308.8 degrees C, respectively, which are remarkably high when compared to those of PPC. The minimum permanent deformation of the copolymers closes to 0, while that of PPC is 173%. The maximum tensile strength of the copolymers is 25.5 MPa higher than that of PPC, reaching 38.4 MPa, and it still has some toughness with the elongation at break of 25%. The above phenomena indicate that MAO that was inserted in PPC chains play a cross-linking role, which results in enhanced thermal stability, dimensional stability, and mechanical strength, comprehensively.
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页数:12
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