Enhanced Interfacial Adhesion by Reactive Carbon Nanotubes: New Route to High-Performance Immiscible Polymer Blend Nanocomposites with Simultaneously Enhanced Toughness, Tensile Strength, and Electrical Conductivity
Source abstract
Abstract
Physically anchoring carbon nanotubes (CNTs) onto the interface of immiscible polymer blends has been extensively reported; however, enhancement of physical properties of the blends has seldom been achieved. Herein, we used CNTs with reactive epoxide groups and long poly(methyl methacrylate) (PMMA) tails as a thermodynamic compatibilizer for immiscible poly vinylidene fluoride/poly l-lactide (PVDF/PLLA) blends. The CNTs acted as an efficient compatibilizer and bridged the two phases through physical entanglement and chemical reaction. The sea-island structure of the blend transformed into a bicontinuous structure for CNT contents greater than 3 wt %. The mechanical properties, including ductility and tensile strength, thermal properties, and electrical conductivities were all enhanced by the CNTs compatibilizer. This strategy thermodynamically compatibilized by reactive nanofillers paves the way for advanced blend nanocomposites.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Sensor and Energy Harvesting Materials · Carbon Nanotubes in Composites · Fiber-reinforced polymer composites
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Material, Chemistry and Chemical Engineering, Hangzhou Normal University, No. 16 Xuelin Rd., Hangzhou 310036, People’s Republic of China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (28)
Show source-provided references
1. 10.1016/j.progpolymsci.2014.04.00210.1016/j.progpolymsci.2014.04.002 ↗
2. 10.1021/ma800683410.1021/ma8006834 ↗
3. 10.1002/polb.2146110.1002/polb.21461 ↗
4. 10.1039/C4RA07473D10.1039/C4RA07473D ↗
5. 10.1021/ma060125+10.1021/ma060125+ ↗
6. 10.1039/C5RA20632D10.1039/C5RA20632D ↗
7. 10.1021/ma301903n10.1021/ma301903n ↗
8. 10.1016/j.polymer.2004.10.00910.1016/j.polymer.2004.10.009 ↗
9. 10.1039/C6RA00218H10.1039/C6RA00218H ↗
10. 10.1016/j.polymer.2010.01.05010.1016/j.polymer.2010.01.050 ↗
11. 10.1007/BF0031080210.1007/BF00310802 ↗
12. 10.1016/j.polymer.2017.11.00410.1016/j.polymer.2017.11.004 ↗
13. 10.1021/acsami.7b0172810.1021/acsami.7b01728 ↗
14. 10.1016/j.polymer.2008.07.01810.1016/j.polymer.2008.07.018 ↗
15. 10.1002/polb.2363810.1002/polb.23638 ↗
16. 10.1016/j.polymer.2003.12.01310.1016/j.polymer.2003.12.013 ↗
17. 10.1016/j.carbon.2014.02.06310.1016/j.carbon.2014.02.063 ↗
18. 10.1016/j.compositesb.2013.07.01210.1016/j.compositesb.2013.07.012 ↗
19. 10.1021/acs.langmuir.7b0308510.1021/acs.langmuir.7b03085 ↗
20. 10.1016/j.carbon.2016.12.04810.1016/j.carbon.2016.12.048 ↗
21. 10.1021/bm801183f10.1021/bm801183f ↗
22. 10.1016/j.eurpolymj.2016.02.02310.1016/j.eurpolymj.2016.02.023 ↗
23. 10.1016/j.eurpolymj.2011.11.01310.1016/j.eurpolymj.2011.11.013 ↗
24. 10.1007/s10853-012-6327-010.1007/s10853-012-6327-0 ↗
25. 10.1021/acsmacrolett.6b0003310.1021/acsmacrolett.6b00033 ↗
26. 10.1021/ma60048a04010.1021/ma60048a040 ↗
27. 10.1021/am900314k10.1021/am900314k ↗
28. 10.1021/acs.macromol.7b0214310.1021/acs.macromol.7b02143 ↗