4.7 Article

A novel zinc chelate complex containing both phosphorus and nitrogen for improving the flame retardancy of low density polyethylene

Journal

JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS
Volume 92, Issue 2, Pages 339-346

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jaap.2011.07.007

Keywords

Zn chelate; alpha-Aminophosphite; Low density polyethylene; Flame retardant

Funding

  1. key scientific and technological innovation team work project of Zhejiang province [2009R50004]
  2. National Science Foundation of Ningbo [201101A6105056]

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A novel metal chelate complex containing phosphorus, nitrogen and zinc (II) ion was synthesized and used as the flame retardant of low density polyethylene (LDPE). The zinc chelate complex was synthesized by reacting zinc acetate with the ligand of tetraethyl (1,2-phenylenebis(azanediyl)) bis (2-hydroxylphenyl methylene) diphosphonate (TEPAPM). The chemical structure of the target Zn-TEPAPM was confirmed by FTIR, (1)H NMR, (13)C NMR and (31)P NMR spectra. The flame retardancy and thermal behavior of LDPE containing various amount of Zn-TEPAPM were investigated by limiting oxygen index test, thermogravimetric (TG) analysis and cone calorimetry. The results show that Zn-TEPAPM can greatly increase the thermal stability, the char formation and smoke suppression ability of LDPE. The TG curves show that even when the filler content of Zn-TEPAPM is as low as 1 wt% in LOPE, the onset degradation temperature of LDPE is increased from 429 degrees C to 442 degrees C, and the maximum degradation temperature is increased from 469 degrees C to 488 degrees C. Also, a reduction of 32% for the peak heat release rate (PHRR) is obtained in the cone test. Moreover, Zn-TEPAPM is demonstrated to be a very effective synergist of ammonium polyphosphate (APP). When 1 wt% of Zn-TEPAPM was introduced into the LDPE/APP (mass ratio 80/19) blend, the PHRR value is reduced by 32%, compared with that of LDPE/APP blend without Zn-TEPAPM, and the char layer becomes more compact and intact. (C) 2011 Elsevier B.V. All rights reserved.

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