Effect of clay with different cation exchange capacity on the morphology and properties of poly(methyl methacrylate)/clay nanocomposites
Source abstract
Abstract
Abstract PMMA/clay nanocomposites were successfully prepared by in situ free‐radical polymerization with the organic modified MMT‐clay using methyl methacrylate monomer and benzoyl peroxide initiator. Two clays with different cation exchange capacity have been used to prepare and compare the several properties. The clays have been modified using Amphoterge K2 by ion exchange reaction to increase the compatibility between the clay and polymer matrices. The modified clays have been characterized by wide‐angle X‐ray diffraction pattern, Fourier transform infrared spectroscopy, and thermogravimetric analysis (TGA). The powdered X‐ray diffraction and transmission electron microscopy techniques were employed to study the morphology of the PMMA/clay nanocomposites which indicate that the modified clays are dispersed in PMMA matrix to form both exfoliated and intercalated PMMA/modified clay nanocomposites. The thermomechanical properties were examined by TGA, differential scanning calorimetry, and dynamic mechanical analysis. Gas permeability analyzer shows the excellent gas barrier property of the nanocomposites, which is in good agreement with the morphology. The optical property was measured by UV–vis spectroscopy which shows that these materials have good optical clarity and UV resistance. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Polymer Nanocomposites and Properties · Polymer Nanocomposite Synthesis and Irradiation · Silicone and Siloxane Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (28)
Show source-provided references
1. 10.1016/S0032-3861(03)00075-210.1016/S0032-3861(03)00075-2 ↗
2. 10.1016/j.polymer.2003.11.03610.1016/j.polymer.2003.11.036 ↗
3. 10.1557/JMR.1993.118510.1557/JMR.1993.1185 ↗
4. 10.1002/adma.1993005060310.1002/adma.19930050603 ↗
5. 10.1002/pat.85210.1002/pat.852 ↗
6. 10.1002/adma.1996008010410.1002/adma.19960080104 ↗
7. 10.1021/cm00059a02310.1021/cm00059a023 ↗
8. 10.1016/S0169-1317(99)00019-810.1016/S0169-1317(99)00019-8 ↗
9. 10.1021/cm00041a00210.1021/cm00041a002 ↗
10. 10.1002/adma.20040126010.1002/adma.200401260 ↗
11. 10.1021/cm960227m10.1021/cm960227m ↗
12. 10.1002/pat.68510.1002/pat.685 ↗
13. 10.1002/pat.68610.1002/pat.686 ↗
14. Schildknecht C.E. · 1956
15. 10.1016/S0032-3861(99)00655-210.1016/S0032-3861(99)00655-2 ↗
16. 10.1021/cm010337f10.1021/cm010337f ↗
17. 10.1016/S0032-3861(00)00419-510.1016/S0032-3861(00)00419-5 ↗
18. 10.1016/j.polymer.2004.03.05810.1016/j.polymer.2004.03.058 ↗
19. 10.1016/j.polymer.2005.08.03610.1016/j.polymer.2005.08.036 ↗
20. 10.1016/j.polymer.2006.07.00510.1016/j.polymer.2006.07.005 ↗
21. 10.1002/(SICI)1097-4628(19990718)73:3<425::AID-APP14>3.0.CO;2-R10.1002/(SICI)1097-4628(19990718)73:3<425::AID-APP14>3.0.CO;2-R ↗
22. 10.1021/cm01165610.1021/cm011656 ↗
23. T.‐Y.Tsai S.‐J.Jong A.‐C.Yeh J.‐B.Chiang andR.Fang U.S. Patent 6 548 159 (2003).
24. 10.1016/j.desal.2007.09.04110.1016/j.desal.2007.09.041 ↗
25. Tsai T.‐Y. · Polym. Compos.
26. 10.1002/pen.2097710.1002/pen.20977 ↗
27. 10.1002/1521-3900(200004)155:1<229::AID-MASY229>3.0.CO;2-R10.1002/1521-3900(200004)155:1<229::AID-MASY229>3.0.CO;2-R ↗
28. 10.1016/j.polymertesting.2005.03.00810.1016/j.polymertesting.2005.03.008 ↗