The synthesis and properties of a reactive flame-retardant unsaturated polyester resin from a phosphorus-containing diacid

被引:84
|
作者
Zhang, Chen [1 ,2 ]
Huang, Jun Yi [1 ,3 ]
Liu, Shu Mei [1 ]
Zhao, Jian Qing [1 ]
机构
[1] S China Univ Technol, Coll Mat Sci & Engn, Guangzhou 510640, Peoples R China
[2] S China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Guangdong, Peoples R China
[3] S China Univ Technol, Key Lab Polymer Proc Engn, Minist Educ, Guangzhou 510640, Peoples R China
关键词
unsaturated polyester resin; synthesis; thermal stability; flame retardance; THERMAL-DEGRADATION; EPOXY; BEHAVIOR; CHEMISTRY;
D O I
10.1002/pat.1670
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A transparent flame-retardant unsaturated polyester resin (FR-UPR) was obtained by reacting propylene glycol (PG) with maleic anhydride (MA), phthalic anhydride (PA), and 9,10-dihydro-10[2,3-di(hydroxy carbonyl) propyl]-10-phosphaphenanthrene-10-oxide (DDP) synthesized from 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO) and itaconic acid (ITA). The chemical structure of the resulting FR-UPR was confirmed by FTIR, H-1-NMR and P-31-NMR. The average molecular weight and viscosity of the FR-UPR were determined by gel permeation chromatography (GPC) and viscometer, respectively. Thermal stability was studied by thermogravimetric analysis (TGA) both in air and nitrogen to determine the thermal decomposition mechanism, and the apparent activation energy (E-a) was calculated by both the Kissinger and Ozawa methods. Compared to unsaturated polyester resin (UPR), the higher E-a of FR-UPR3 implied an improved thermal stability. According to variations of the limited oxygen index (LOI) values, the UL 94 rating of vertical burning test and scanning electronmicroscopy (SEM) photographs of char residues, the flame retardance of cured FR-UPR was enhanced with increasing DDP content. The study of fire reaction tests, using a cone calorimeter, suggested that there was a significant reduction of flammability in the FR-UPR. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:1768 / 1777
页数:10
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