Fast-Scanning Chip-Calorimetry Measurement of Crystallization Kinetics of Poly(Glycolic Acid)

被引:13
作者
Chen, Yongxuan [1 ]
Xie, Kefeng [1 ]
He, Yucheng [1 ]
Hu, Wenbing [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Dept Polymer Sci & Engn, State Key Lab Coordinat Chem, Nanjing 210023, Peoples R China
关键词
polymer crystallization; crystallization kinetics; thermal analysis; poly(glycolic acid); poly((L)-lactic acid); FLASH DSC; POLY(L-LACTIC ACID); POLYMER CRYSTALLIZATION; INFRARED-SPECTROSCOPY; CRYSTAL NUCLEATION; CONFORMATION; BEHAVIOR; PROGRESS; FIBER; SPUN;
D O I
10.3390/polym13060891
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report fast-scanning chip-calorimetry measurement of isothermal crystallization kinetics of poly(glycolic acid) (PGA) in a broad temperature range. We observed that PGA crystallization could be suppressed by cooling rates beyond -100 K s(-1) and, after fast cooling, by heating rates beyond 50 K s(-1). In addition, the parabolic curve of crystallization half-time versus crystallization temperature shows that PGA crystallizes the fastest at 130 degrees C with the minimum crystallization half-time of 4.28 s. We compared our results to those of poly((L)-lactic acid) (PLLA) with nearby molecular weights previously reported by Androsch et al. We found that PGA crystallizes generally more quickly than PLLA. In comparison to PLLA, PGA has a much smaller hydrogen side group than the methyl side group in PLLA; therefore, crystal nucleation is favored by the higher molecular mobility of PGA in the low temperature region as well as by the denser molecular packing of PGA in the high temperature region, and the two factors together decide the higher crystallization rates of PGA in the whole temperature range.
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页数:10
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