Thermal and dynamic mechanical properties of attapulgite reinforced poly(butylene succinate‐co‐1,2‐ octanediol succinate) nanocomposites
Source abstract
Abstract
Attapulgite (ATP)‐reinforced poly(butylene succinate‐co‐1,2‐octanediol succinate) nanocomposites were fabricated using an in situ two‐step polymerization method. The transmission electron microscopy (TEM) results showed a superior interfacial linkage between ATP and PBS matrix. The isothermal crystallization kinetics results showed that ATP can effectively act as a nucleating agent, resulting in an enhancement on the crystallization temperature and crystallization rate. The incorporation of ATP nanoparticles probably induced heterogeneous nucleation that made the lower activation energy. The equilibrium melting temperature ( ) of the ATP reinforced branched copolymer also had little difference with the homogeneous PBS. The temperature at an initial thermal degradation was improved for the ATP reinforced branched nanocomposites. The dynamic mechanical analysis (DMA) results showed that there was a significant increase of storage modulus (E′) in an overall temperature range of all ATP reinforced nanocomposites. ATP had a strong effect on the elastic properties of the homogeneous PBS matrix. POLYM. COMPOS., 34:1126–1135, 2013. © 2013 Society of Plastics Engineers
Source: crossref · Quality: baseline
Research context
OpenAlex topics: biodegradable polymer synthesis and properties · Polymer Nanocomposites and Properties · Polymer crystallization and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical Engineering and Environment Beijing Institute of Technology Beijing 100081 China
Department of Chemical Engineering Institute of Polymer Science and Engineering, Tsinghua University Beijing 100084 China
Funding
National High-Tech R&D Program of China · National Natural Science Foundation of China
References (29)
Show source-provided references
1. 10.1023/A:102020082243510.1023/A:1020200822435 ↗
2. 10.1002/pola.1995.08033070710.1002/pola.1995.080330707 ↗
3. 10.1021/ma021728y10.1021/ma021728y ↗
4. 10.1002/biot.20100013610.1002/biot.201000136 ↗
5. 10.1002/app.3216810.1002/app.32168 ↗
6. 10.1016/j.polymdegradstab.2009.01.00910.1016/j.polymdegradstab.2009.01.009 ↗
7. 10.1166/jnn.2006.36810.1166/jnn.2006.368 ↗
8. 10.1016/j.polymdegradstab.2008.02.00710.1016/j.polymdegradstab.2008.02.007 ↗
9. 10.1016/j.eurpolymj.2008.07.03510.1016/j.eurpolymj.2008.07.035 ↗
10. 10.1016/j.polymertesting.2010.03.00710.1016/j.polymertesting.2010.03.007 ↗
11. 10.1016/S0070-4571(08)70706-410.1016/S0070-4571(08)70706-4 ↗
12. 10.1016/j.polymer.2006.07.00110.1016/j.polymer.2006.07.001 ↗
13. 10.1002/macp.20080044110.1002/macp.200800441 ↗
14. 10.1016/j.tca.2004.09.00110.1016/j.tca.2004.09.001 ↗
15. 10.1002/polb.2034710.1002/polb.20347 ↗
16. 10.1002/macp.20060016310.1002/macp.200600163 ↗
17. 10.1002/macp.20070008410.1002/macp.200700084 ↗
18. 10.1016/j.polymer.2003.10.04510.1016/j.polymer.2003.10.045 ↗
19. 10.1016/j.polymertesting.2006.10.00510.1016/j.polymertesting.2006.10.005 ↗
20. 10.1002/pc.2102310.1002/pc.21023 ↗
21. 10.1021/ma070255y10.1021/ma070255y ↗
22. 10.1002/(SICI)1099-0488(19990701)37:13<1357::AID-POLB2>3.0.CO;2-Q10.1002/(SICI)1099-0488(19990701)37:13<1357::AID-POLB2>3.0.CO;2-Q ↗
23. 10.1002/pc.2105910.1002/pc.21059 ↗
24. 10.1002/app.3322210.1002/app.33222 ↗
25. 10.1021/ma980747y10.1021/ma980747y ↗
26. 10.1002/pi.84810.1002/pi.848 ↗
27. 10.1002/pat.193710.1002/pat.1937 ↗
28. 10.1002/mame.20110004210.1002/mame.201100042 ↗
29. 10.1002/app.3035310.1002/app.30353 ↗