High efficiency intumescent flame retardancy between Hexakis (4-nitrophenoxy) cyclotriphosphazene and ammonium polyphosphate on ABS

被引:23
作者
Cao, Xilei [1 ]
Yang, Yunyun [1 ]
Luo, Hang [1 ]
Cai, Xufu [1 ]
机构
[1] Sichuan Univ, Dept Polymer Sci & Mat, State Key Lab Polymer Mat Engn, Chengdu 610065, Sichuan, Peoples R China
关键词
Intumescence flame retardant; Hexakis(4-nitrophenoxy); cyclotriphosphazene (HNTP); Ammonium polyphosphate (APP); Acrylonitrile-butadiene-styrene (ABS); MECHANICAL-PROPERTIES; AGENT; FORMULATIONS; COMPOSITES; COMBUSTION; PHOSPHATE; MIXTURES; POLYMERS; SYSTEMS;
D O I
10.1016/j.polymdegradstab.2017.07.022
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Hexakis(4-nitrophenoxy) cyclotriphosphazene (HNTP) with ammonium polyphosphate (APP) were added to acrylonitrile butadiene styrene copolymer (ABS) to improve the intumescent flammability and thermal properties of ABS. The effect of intumescent flame retardancy was characterized by limited oxygen index (LOI), vertical burning test (UL-94), thermos gravimetric analysis (TGA) tests, Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). When the loading of ABS, HNTP and APP were 70,15 and 15%, respectively, the LOI value reached 25.6 and UL-94 test was V-0. The TGA showed the high char yield of ABS/30%HNTP system at high temperatures. The experimental and theoretical TG curves and FTIR indicated that HNTP and APP promoted the form of cross-link structure, which acted as a barrier near the surface of material. The SEM further revealed the formation morphology of intumescent charred layer on ABS/15%HNTP/15%APP system. Tensile tests provided the possibility of using HNTP at high temperature. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:259 / 265
页数:7
相关论文
共 22 条
[1]  
Bourbigot S, 2000, FIRE MATER, V24, P201, DOI 10.1002/1099-1018(200007/08)24:4<201::AID-FAM739>3.0.CO
[2]  
2-D
[3]   4A zeolite synergistic agent in new flame retardant intumescent formulations of polyethylenic polymers - Study of the effect of the constituent monomers [J].
Bourbigot, S ;
LeBras, M ;
Delobel, R ;
Breant, P ;
Tremillon, JM .
POLYMER DEGRADATION AND STABILITY, 1996, 54 (2-3) :275-287
[4]   Modeling of heat transfer of a polypropylene-based intumescent system during combustion [J].
Bourbigot, S ;
Duquesne, S ;
Leroy, JM .
JOURNAL OF FIRE SCIENCES, 1999, 17 (01) :42-56
[5]   STUDY OF THE MECHANISM OF INTUMESCENCE IN FIRE RETARDANT POLYMERS .6. MECHANISM OF ESTER FORMATION IN AMMONIUM POLYPHOSPHATE PENTAERYTHRITOL MIXTURES [J].
CAMINO, G ;
COSTA, L ;
TROSSARELLI, L ;
COSTANZI, F ;
PAGLIARI, A .
POLYMER DEGRADATION AND STABILITY, 1985, 12 (03) :213-228
[6]  
[陈晓平 Chen Xiaoping], 2010, [中国塑料, China Plastics], V24, P1
[7]   Mathematical model for the nonsteady decomposition of intumescent coatings [J].
Di Blasi, C ;
Branca, C .
AICHE JOURNAL, 2001, 47 (10) :2359-2370
[8]   Development of fire resistant PET fibrous structures based on phosphinate-POSS blends [J].
Didane, Nizar ;
Giraud, Stephane ;
Devaux, Eric ;
Lemort, Guillaume .
POLYMER DEGRADATION AND STABILITY, 2012, 97 (06) :879-885
[9]   LDPE/LLDPE/APP intumescent flame retardant systems: molding parameters and properties [J].
Guo, Yuhua ;
Guo, Jianjun ;
Huang, Zhen ;
Teng, Lijun .
EQUIPMENT MANUFACTURING TECHNOLOGY AND AUTOMATION, PTS 1-3, 2011, 317-319 :112-+
[10]   Thermal degradation mechanism and flame retardancy of MQ silicone/epoxy resin composites [J].
Jia, Pei ;
Liu, Hanchao ;
Liu, Qiang ;
Cai, Xufu .
POLYMER DEGRADATION AND STABILITY, 2016, 134 :144-150