Allyl phosphonium salt–modified clay for photocured coatings: Influence on the properties of polyester acrylate‐based coatings
Source abstract
Abstract
In this study, bentonite clay was modified with a phosphonium salt and this modified clay was used to prepare polyester acrylate based coatings to improve their flame retardancy and mechanical properties. Photocured composites were prepared with 1, 2, and 3 wt% phosphonium salt modified clay and for comparison 1 wt% nonmodified clay containing composites were also prepared. Modified clay displayed good dispersion properties due to its increased basal spacing. Composites were characterized by FT‐IR and XRD measurements. According to XRD results, it was found that the modified clay was exfoliated in the composites. Furthermore, we investigated the effect of allyl phosphonium salt modified clay on the thermal, mechanical, and flame retardant properties of polyester acrylate based composites coatings. When compared with neat clay containing coatings, modified clay containing photocured coatings exhibited increased modulus and enhanced thermal properties due to increased crosslinking density. Moreover, the presence of the phosphonium salt enhanced the flame retardancy of the polyester based coatings. POLYM. COMPOS., 36:946–954, 2015. © 2014 Society of Plastics Engineers
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Research context
OpenAlex topics: Flame retardant materials and properties · Polymer Nanocomposites and Properties · Polymer composites and self-healing
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Istanbul Technical University, Applied Research Center of Materials Science and Production Technology Maslak 34469 Istanbul Turkey
Marmara University, Faculty of Art and Science Department of Chemistry 34722 Istanbul Turkey
References (30)
Show source-provided references
1. 10.1177/073168440708425410.1177/0731684407084254 ↗
2. 10.1021/cm020391b10.1021/cm020391b ↗
3. 10.1016/S0032-3861(01)00650-410.1016/S0032-3861(01)00650-4 ↗
4. 10.1021/ma961786h10.1021/ma961786h ↗
5. 10.1016/j.jcis.2004.09.06610.1016/j.jcis.2004.09.066 ↗
6. 10.1021/cm020705v10.1021/cm020705v ↗
7. 10.1016/j.materresbull.2005.08.01910.1016/j.materresbull.2005.08.019 ↗
8. 10.1016/j.eurpolymj.2007.09.02410.1016/j.eurpolymj.2007.09.024 ↗
9. 10.1016/j.polymer.2010.02.00310.1016/j.polymer.2010.02.003 ↗
10. 10.1016/j.porgcoat.2004.10.00310.1016/j.porgcoat.2004.10.003 ↗
11. 10.1023/A:102081841492710.1023/A:1020818414927 ↗
12. 10.1080/0021846950934241310.1080/00218469509342413 ↗
13. 10.1016/j.reactfunctpolym.2010.11.01110.1016/j.reactfunctpolym.2010.11.011 ↗
14. 10.1002/polb.2121210.1002/polb.21212 ↗
15. 10.1016/j.clay.2011.08.00210.1016/j.clay.2011.08.002 ↗
16. 10.1016/j.eurpolymj.2008.04.00510.1016/j.eurpolymj.2008.04.005 ↗
17. 10.4236/gsc.2012.2100410.4236/gsc.2012.21004 ↗
18. 10.5419/bjpg2012-001410.5419/bjpg2012-0014 ↗
19. 10.4186/ej.2012.16.3.1310.4186/ej.2012.16.3.13 ↗
20. 10.1179/174327807X19686110.1179/174327807X196861 ↗
21. 10.1016/j.clay.2011.05.01010.1016/j.clay.2011.05.010 ↗
22. 10.1016/j.eurpolymj.2006.06.01610.1016/j.eurpolymj.2006.06.016 ↗
23. 10.1016/j.polymer.2005.05.01810.1016/j.polymer.2005.05.018 ↗
24. Inceoglu F. · 2009
25. 10.1002/pc.2063610.1002/pc.20636 ↗
26. 10.1016/j.porgcoat.2010.03.01510.1016/j.porgcoat.2010.03.015 ↗
27. 10.1016/j.polymdegradstab.2007.10.00510.1016/j.polymdegradstab.2007.10.005 ↗
28. 10.5012/bkcs.2011.32.6.193610.5012/bkcs.2011.32.6.1936 ↗
29. 10.1021/cm020705v10.1021/cm020705v ↗
30. 10.1016/j.progpolymsci.2010.03.00110.1016/j.progpolymsci.2010.03.001 ↗