Structural characterization, thermal properties, and density functional theory studies of PMMA‐maghemite hybrid material
Source abstract
Abstract
Maghemite (γ‐Fe2O3)‐poly(methyl methacrylate) (PMMA) nanocomposites were prepared by grafting 3‐(trimethoxy‐silyl) propyl methacrylate on the surface of maghemite nanoparticles, this process being followed by methyl methacrylate radical polymerization. Three different hybrids with 0.1, 0.5, and 2.5 wt% of maghemite nanoparticles were studied. The results indicate that these nanocomposites consist of a homogeneous PMMA matrix in which maghemite nanoparticles with a bimodal size distribution are embedded. The existence of covalent bonding between silane monomers and atoms on the maghemite surface was evidenced. AFM images showed a clear increase in surface roughness for increasing maghemite content. The thermal stability of PMMA‐maghemite nanocomposites is higher than that of pure PMMA and increases for increasing maghemite content. The results of our theoretical studies indicate that the electron density in the maghemite nanoparticle is not homogenous, the low electron density volumes being supposed to be radical trappers during PMMA decomposition, thus acting as a thermal stabilizer. POLYM. COMPOS., 51–60, 2016. © 2014 Society of Plastics Engineers
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Research context
OpenAlex topics: Polymer Nanocomposites and Properties · Polymer Science and PVC · Polymer crystallization and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry Federal University of Lavras 37200‐000 Lavras Minas Gerais Brazil
Institute for Chemical Technology and Polymer Chemistry (ITCP) Karlsruhe Institute of Technology (KIT) 76131 Karlsruhe Germany
Department of Chemistry Federal University of Sergipe 49500‐000 Itabaiana Sergipe Brazil
Department of Applied Physics Physics Institute, University of São Paulo 05508‐900 Sao Paulo SP Brazil
Funding
CNPq, CAPES
References (32)
Show source-provided references
1. 10.1039/b509097k10.1039/b509097k ↗
2. 10.1021/cr068035q10.1021/cr068035q ↗
3. 10.1039/b507309j10.1039/b507309j ↗
4. Sanchez C. · New J. Chem. · 1994 · 18 · 1007
5. 10.1016/S0304-8853(00)01255-510.1016/S0304-8853(00)01255-5 ↗
6. 10.1080/1558372070127129410.1080/15583720701271294 ↗
7. 10.1002/pc.2079310.1002/pc.20793 ↗
8. 10.1002/app.3125810.1002/app.31258 ↗
9. 10.1016/j.eurpolymj.2006.12.01210.1016/j.eurpolymj.2006.12.012 ↗
10. 10.1002/pola.2252310.1002/pola.22523 ↗
11. 10.1007/s00396-009-2013-410.1007/s00396-009-2013-4 ↗
12. 10.1002/app.3020110.1002/app.30201 ↗
13. 10.1002/978352761227710.1002/9783527612277 ↗
14. 10.1002/jcc.105610.1002/jcc.1056 ↗
15. 10.1016/j.jssc.2006.09.03310.1016/j.jssc.2006.09.033 ↗
16. 10.1002/jbm.a.3090910.1002/jbm.a.30909 ↗
17. 10.1016/j.jenvman.2010.06.00310.1016/j.jenvman.2010.06.003 ↗
18. 10.1016/S0169-1317(02)00156-410.1016/S0169-1317(02)00156-4 ↗
19. 10.1016/j.matchemphys.2011.04.04410.1016/j.matchemphys.2011.04.044 ↗
20. 10.1016/S0924-2031(02)00009-710.1016/S0924-2031(02)00009-7 ↗
21. 10.1107/S002188989500529210.1107/S0021889895005292 ↗
22. Beaucage G.J. · 1995
23. Glatter O. · 1982
24. 10.1016/S0040-6031(00)00661-410.1016/S0040-6031(00)00661-4 ↗
25. 10.1021/ma00162a01010.1021/ma00162a010 ↗
26. 10.1021/cm010451y10.1021/cm010451y ↗
27. 10.1039/c3ra44388d10.1039/c3ra44388d ↗
28. 10.1016/j.polymdegradstab.2007.06.00310.1016/j.polymdegradstab.2007.06.003 ↗
29. 10.1007/s10853-010-4639-510.1007/s10853-010-4639-5 ↗
30. 10.1088/0953-8984/22/25/25540110.1088/0953-8984/22/25/255401 ↗
31. 10.1139/v92-31610.1139/v92-316 ↗
32. 10.1016/j.saa.2013.08.02910.1016/j.saa.2013.08.029 ↗