journal article·2018-02

Study on the Crystallization Activation Energy of Poly (L-lactic acid) Nucleated with P-tert-butylcalix[8]arene

Yaoqi Shi, Liang Wen, Zhong Xin

Polymers and Polymer Composites· Volume 26· Issue 2
Publisher page

Abstract

The crystallization activation energy (Δ E) of a polymer comprises the nucleation activation energy Δ F and the transport activation energy Δ E * . In this paper, the Δ E of poly (L-lactic acid) (PLLA) nucleated with nucleating agent p- tert-butylcalix[8]arene (tBC8) was calculated. The results showed that the Δ E of nucleated PLLA was 165.97 kJ/mol, which is higher than that of pure PLLA. The reason why Δ E of PLLA increased when incorporating nucleating agent was studied. The increment of glass transition temperature ( Tg) for nucleated PLLA revealed that the polymer chain mobility was restricted by tBC8, which was considered as the reason for the increase of Δ E*. Further, polyethylene glycol (PEG) was added to improve the chain mobility, thus eliminated the variation of the transport activation energy Δ E* caused by tBC8. Then the effect of the increment of crystallization temperature range on the increase of Δ F was also taken into consideration. It was concluded that both decreasing the mobility of chain segments and increasing the crystallization temperature range caused an increase of Δ E for PLLA/tBC8.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: biodegradable polymer synthesis and properties · Polymer crystallization and properties · Polymer Nanocomposites and Properties

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Shanghai Key Laboratory of Multiphase Materials Chemical Engineering, College of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China

State Key Laboratory of Chemical Engineering, College of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China

References (27)

Show source-provided references
1. Mandelkern L. · 1964
2. 10.1021/ma050739z10.1021/ma050739z ↗
3. 10.1007/s10965-016-1179-y10.1007/s10965-016-1179-y ↗
4. 10.1007/s10853-016-9793-y10.1007/s10853-016-9793-y ↗
5. 10.1016/j.progpolymsci.2007.02.00110.1016/j.progpolymsci.2007.02.001 ↗
6. 10.1021/ma020237a10.1021/ma020237a ↗
7. 10.1021/ma034172310.1021/ma0341723 ↗
8. 10.1002/app.3623610.1002/app.36236 ↗
9. 10.1021/ma047331710.1021/ma0473317 ↗
10. 10.6028/jres.057.02610.6028/jres.057.026 ↗
11. 10.1002/polb.2115410.1002/polb.21154 ↗
12. 10.1002/polb.2072210.1002/polb.20722 ↗
13. 10.1016/j.polymer.2008.04.01210.1016/j.polymer.2008.04.012 ↗
14. 10.1002/app.2968910.1002/app.29689 ↗
15. 10.1016/S0032-3861(98)00743-510.1016/S0032-3861(98)00743-5 ↗
16. 10.1002/polb.2148310.1002/polb.21483 ↗
17. 10.15227/orgsyn.068.024310.15227/orgsyn.068.0243 ↗
18. 10.1295/polymj.29.65710.1295/polymj.29.657 ↗
19. 10.1021/ja01619a00810.1021/ja01619a008 ↗
20. 10.1002/(SICI)1099-0488(19970130)35:2<359::AID-POLB12>3.0.CO;2-H10.1002/(SICI)1099-0488(19970130)35:2<359::AID-POLB12>3.0.CO;2-H ↗
21. 10.1021/ma00057a04210.1021/ma00057a042 ↗
22. 10.1021/acsami.6b0070410.1021/acsami.6b00704 ↗
23. 10.1002/app.4412010.1002/app.44120 ↗
24. 10.1002/pat.386410.1002/pat.3864 ↗
25. 10.1016/S0032-3861(03)00609-810.1016/S0032-3861(03)00609-8 ↗
26. 10.1021/bm050323t10.1021/bm050323t ↗
27. 10.1021/ma901547a10.1021/ma901547a ↗