Development of phosphazene imine‐modified epoxy composites for low dielectric, antibacterial activity, and UV shielding applications
Source abstract
Abstract
In this work, phosphazene modified imine was prepared and its molecular structure was confirmed using FTIR and 1H NMR analysis. The modified phosphazene imine (PZ imine) of different weight percentages was incorporated into DGBEA epoxy resin to obtain composites and the formation of composites was confirmed by FTIR analysis. The composites were subjected to thermal, radiation resistant, electrical, and antibacterial studies. Data resulted from thermal, UV absorption, antibacterial, and surface behavior studies indicate that PZ imine reinforced epoxy composites possess higher thermal stability, enhanced zone of inhibition, better UV shielding, improved hydrophobic behavior and lower value of dielectric constant than those of neat epoxy matrix. The morphology of the samples was analyzed using high resolution transmission electron microsope (HRTEM), which ascertained the homogeneous dispersion of PZ imine in epoxy matrix with fibrous structure. POLYM. COMPOS., 38:E24–E33, 2017. © 2015 Society of Plastics Engineers
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Research context
OpenAlex topics: Epoxy Resin Curing Processes · Synthesis and properties of polymers · Polymer Nanocomposites and Properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering Polymer Composite Lab, Anna University Chennai 600025 Tamil Nadu India
Mechanical Engineering Program, Texas a&M University at Qatar, Engineering Building, Education City Doha Qatar
Funding
University Grants Commission
References (30)
Show source-provided references
1. 10.1002/(SICI)1099-0518(199702)35:3<565::AID-POLA22>3.0.CO;2-L10.1002/(SICI)1099-0518(199702)35:3<565::AID-POLA22>3.0.CO;2-L ↗
2. 10.1177/095400831038114710.1177/0954008310381147 ↗
3. 10.1016/j.polymdegradstab.2008.09.00210.1016/j.polymdegradstab.2008.09.002 ↗
4. 10.1177/095400831456305710.1177/0954008314563057 ↗
5. 10.1007/s11249-014-0309-010.1007/s11249-014-0309-0 ↗
6. 10.1016/j.eurpolymj.2011.01.00710.1016/j.eurpolymj.2011.01.007 ↗
7. 10.1177/095400831039763410.1177/0954008310397634 ↗
8. 10.1016/j.polymdegradstab.2009.01.00810.1016/j.polymdegradstab.2009.01.008 ↗
9. 10.1007/BF0029351410.1007/BF00293514 ↗
10. 10.1016/S0014-3057(96)00214-510.1016/S0014-3057(96)00214-5 ↗
11. 10.1002/polb.1990.09028060110.1002/polb.1990.090280601 ↗
12. 10.1007/BF0111429310.1007/BF01114293 ↗
13. 10.1002/app.2723410.1002/app.27234 ↗
14. 10.1002/maco.20100578810.1002/maco.201005788 ↗
15. 10.3144/expresspolymlett.2007.4610.3144/expresspolymlett.2007.46 ↗
16. Murray P.R. · 1995
17. 10.1002/app.1279610.1002/app.12796 ↗
18. 10.1016/j.porgcoat.2012.12.01010.1016/j.porgcoat.2012.12.010 ↗
19. 10.1016/j.compscitech.2007.03.00410.1016/j.compscitech.2007.03.004 ↗
20. 10.1016/S0300-9440(99)00070-310.1016/S0300-9440(99)00070-3 ↗
21. 10.1002/mame.20070031810.1002/mame.200700318 ↗
22. 10.1002/polb.1044510.1002/polb.10445 ↗
23. 10.1016/j.polymdegradstab.2012.02.01310.1016/j.polymdegradstab.2012.02.013 ↗
24. 10.1016/j.carbpol.2011.07.05510.1016/j.carbpol.2011.07.055 ↗
25. Raslan W.M. · Mater. Sci. Appl. · 2011 · 2 · 1432
26. 10.1016/j.cclet.2013.01.01110.1016/j.cclet.2013.01.011 ↗
27. 10.1016/j.polymer.2006.01.07110.1016/j.polymer.2006.01.071 ↗
28. 10.1002/aoc.17910.1002/aoc.179 ↗
29. 10.1002/jbm.a.3073710.1002/jbm.a.30737 ↗
30. 10.1021/la020237410.1021/la0202374 ↗