Improvement of the chemical, thermal, mechanical and morphological properties of polyethylene terephthalate–graphene particle composites
Source abstract
Abstract
The graphene powder was used as a reinforcement in polyethylene terephthalate (PET) with various weight percentages 0.1, 0.5, 1 and 2 wt%. To prepare PET/graphene powder composites, melt-mixing process was followed. The crosslinking degree between PET and functionalized graphene increased, which was indicated by carbonyl indexes (Fourier transform infrared spectra) when interfaced with PET. The results of thermal properties showed that adding 2 wt% of graphene composites improved the thermal stability, transition glass temperature $$T_\mathrm{g}$$ , crystallinity temperature point and chemical properties of PET. The results of thermal gravimetric analysis showed that the highest addition of graphene (2 wt%) into the PET slightly improves both the residue yields and thermal stability. The tensile strength of PET was highly increased with the increased loading of graphene, and the elongation was reduced, compared with PET without filler. The results of X-ray diffraction curves showed that 2% incorporation of graphene into PET has good interfacial interaction and higher intensity. The scanning electron microscopy micrographs showed a high compatibility between the pure PET and graphene composite chains.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Graphene research and applications · Carbon Nanotubes in Composites · Polymer Nanocomposites and Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (16)
Show source-provided references
1. Abdul Razak N, Inuwa I, Hassan A S and Samsudin S 2013 Compos. Interfaces 20 50710.1080/15685543.2013.811176 ↗
2. Ávila Córdoba L, Martínez-Barrera G, Barrera Díaz C, Ureña Nuñez F and Loza Yañez A 2013 Int. J. Polym. Sci. 2013 Article ID 76327610.1155/2013/763276 ↗
3. Koysuren O, Yesil S and Bayram G 2010 J. Appl. Polym. Sci. 118 304110.1002/app.32727 ↗
4. Lim S and Chow W 2012 J. Appl. Polym. Sci. 123 317310.1002/app.34980 ↗
5. Liu W, Tian X, Cui P, Li Y, Zheng K and Yang Y 2004 J. Appl. Polym. Sci. 91 122910.1002/app.13284 ↗
6. Moniruzzaman M and Winey K I 2006 Macromolecules 39 519410.1021/ma060733p ↗
7. Chen H, Li Y, Zhang F, Zhang G and Fan X 2011 J. Mater. Chem. B 21 1765810.1039/c1jm13356j ↗
8. Chen Z 2013 The crystallization of poly (ethylene terephthalate) studied by thermal analysis and FTIR spectroscopy (Doctoral dissertation, University of Birmingham)
9. Dideykin A, Aleksenskiy A, Kirilenko D, Brunkov P, Goncharov V, Baidakova M et al 2011 Diamond Relat. Mater. 20 10510.1016/j.diamond.2010.10.007 ↗
10. Hu K, Kulkarni D D, Choi I and Tsukruk V V 2014 Prog. Polym. Sci. 39 193410.1016/j.progpolymsci.2014.03.001 ↗
11. Huang L, Zhan R and Lu Y 2006 J. Reinf. Plast. Compos. 25 100110.1177/0731684406065131 ↗
12. Huang X, Qi X, Boey F and Zhang H 2012 Chem. Soc. Rev. 41 66610.1039/C1CS15078B ↗
13. Jiang C H, Xu X B and Li Z M 2007 J. Macromol. Sci. B 47 1010.1080/15568310701744182 ↗
14. Joon Choi W, Kim H J K, Han Yoon K, Hyeong Kwon O and Hwang C I K 2006 J. Appl. Polym. Sci. 100 487510.1002/app.23268 ↗
15. Khalaf E and Awad S 2017 JACS 3 426
16. Santos P and Pezzin S H 2003 J. Mater. Process. Technol. 143 51710.1016/S0924-0136(03)00391-1 ↗