journal article·2025-02-28Open access

Phosphonate-Functionalized Polypropylenes: Single-Component Flame Retardants

Alexander Evans, Louis J. Morris, Zoë R. Turner, Dermot O’Hare

ACS Applied Polymer Materials· Volume 7· Issue 4

Abstract

High Resolution Image Download MS PowerPoint Slide Phosphonate-modified polypropylenes ( PP R; R = PPr, P(O)(O i Pr) 2; PPh, P(O)(OPh) 2 ) have been prepared via a two-step synthesis and display enhanced thermal stability, offering potential as compatible single-component flame-retardant additives for PP systems. PP typically displays high flammability and poor fire resistance, which consequently restricts applications. Solution-phase copolymerization of propylene and 11-bromo-1-undecene using commercial rac -ethylenebis(indenyl)zirconium dichloride afforded poly(propylene)- co -(11-bromo-1-undecene) with tunable comonomer incorporation levels up to 8.1 mol %. Solvent-free, quantitative, postmodification of pendent bromine with phosphite esters yielded alkyl ( PP PPr ) and aryl ( PP PPh ) phosphonate-modified PPs. Increased thermal stability (higher T 10%, T 50%, T max, and %residue at 700 °C) in a synthetic air atmosphere was determined by thermogravimetric analysis with respect to PP . Microscale combustion calorimetry of both PP PPr and PP PPh indicates lower values of heat release capacity, peak heat release rate, and total heat release compared to that of PP, indicating enhanced flame retardancy. Both PP PPr and PP PPh can be easily blended with PP at PP: PP R weight ratios of 80:20, 90:10, 95:5, and 99:1, respectively. The polymer blends demonstrated higher thermal stability than the homopolymer, and so such PP-compatible PP R offers an alternate strategy for improving the flame-retardant properties of PP-based materials, which circumvents additive leaching while limiting disruption to the mechanical strength of the base PP material.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Flame retardant materials and properties

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Chemistry Research Laboratory, Department of Chemistry, University of Oxford, 12 Mansfield Road, OX1 3TA Oxford, U.K.

Funding

SCG Chemicals · University of Oxford

References (55)

Show source-provided references
1. 10.1021/ja01611a10910.1021/ja01611a109 ↗
2. 10.1002/ange.1955067161010.1002/ange.19550671610 ↗
3. 10.3390/ma1324575610.3390/ma13245756 ↗
4. 10.1016/j.ejpe.2016.02.00310.1016/j.ejpe.2016.02.003 ↗
5. 10.3390/molecules2521515710.3390/molecules25215157 ↗
6. John M. J. · 2019 · 4310.1016/B978-0-08-102177-4.00002-1 ↗
7. 10.1002/app.1991.07043091010.1002/app.1991.070430910 ↗
8. 10.1080/00102202.2016.120818710.1080/00102202.2016.1208187 ↗
9. 10.1039/C8EM00515J10.1039/C8EM00515J ↗
10. 10.1016/j.envint.2014.01.00610.1016/j.envint.2014.01.006 ↗
11. 10.2533/00094290377767894810.2533/000942903777678948 ↗
12. 10.1021/acs.accounts.5b0018010.1021/acs.accounts.5b00180 ↗
13. Wang Y. Z. · 2008 · 6710.1533/9781845694701.1.67 ↗
14. Levchik S. V. · 2008 · 4110.1533/9781845694701.1.41 ↗
15. 10.1002/pat.155010.1002/pat.1550 ↗
16. 10.1016/j.chemosphere.2012.03.06710.1016/j.chemosphere.2012.03.067 ↗
17. Hörold S. · 2014 · 22110.1016/B978-0-444-53808-6.00006-8 ↗
18. 10.1002/anie.20171173510.1002/anie.201711735 ↗
19. 10.3390/ma310471010.3390/ma3104710 ↗
20. 10.3390/ma1005045510.3390/ma10050455 ↗
21. 10.1177/07349041920100060210.1177/073490419201000602 ↗
22. 10.1177/07349041960140060210.1177/073490419601400602 ↗
23. 10.1002/app.3439810.1002/app.34398 ↗
24. 10.3390/ma1201015210.3390/ma12010152 ↗
25. 10.1021/ie101737n10.1021/ie101737n ↗
26. 10.1039/c4ta01030b10.1039/c4ta01030b ↗
27. 10.1002/app.4902310.1002/app.49023 ↗
28. 10.1016/S1003-6326(14)63292-110.1016/S1003-6326(14)63292-1 ↗
29. 10.1002/pat.326110.1002/pat.3261 ↗
30. 10.1016/S0141-3910(01)00184-710.1016/S0141-3910(01)00184-7 ↗
31. 10.1002/pat.116710.1002/pat.1167 ↗
32. 10.1007/s11426-015-5427-510.1007/s11426-015-5427-5 ↗
33. 10.1039/C8PY01772G10.1039/C8PY01772G ↗
34. 10.1039/b311405h10.1039/b311405h ↗
35. 10.1039/D3PY00143A10.1039/D3PY00143A ↗
36. 10.1021/acs.macromol.4c0210210.1021/acs.macromol.4c02102 ↗
37. 10.1002/pola.2740910.1002/pola.27409 ↗
38. 10.1002/pol.2021048810.1002/pol.20210488 ↗
39. 10.1021/cr980469110.1021/cr9804691 ↗
40. 10.1016/j.tetlet.2015.02.12610.1016/j.tetlet.2015.02.126 ↗
41. 10.1002/app.1326710.1002/app.13267 ↗
42. 10.1002/pc.2371610.1002/pc.23716 ↗
43. 10.1016/j.jbbm.2003.10.00110.1016/j.jbbm.2003.10.001 ↗
44. 10.1177/095400831875649610.1177/0954008318756496 ↗
45. 10.1021/ie401662x10.1021/ie401662x ↗
46. 10.1177/095400832093739210.1177/0954008320937392 ↗
47. 10.1002/pen.2087110.1002/pen.20871 ↗
48. 10.1002/pat.158310.1002/pat.1583 ↗
49. 10.1039/c0jm03959d10.1039/c0jm03959d ↗
50. 10.1002/pen.2087110.1002/pen.20871 ↗
51. Coleman E. A. · 2017 · 48910.1016/B978-0-323-39040-8.00021-3 ↗
52. 10.1016/j.compositesb.2017.01.04910.1016/j.compositesb.2017.01.049 ↗
53. 10.1016/j.matdes.2015.10.00710.1016/j.matdes.2015.10.007 ↗
54. 10.1016/j.proeng.2016.01.13010.1016/j.proeng.2016.01.130 ↗
55. 10.1007/s11998-018-0069-010.1007/s11998-018-0069-0 ↗