Influence of poly (dihydroxybiphenyl borate) on the curing behaviour and thermal pyrolysis mechanism of phenolic resin

被引:37
作者
Wang, Shujuan [1 ]
Xing, Xiaolong [1 ]
Wang, Ya'nan [1 ]
Wang, Wen [1 ]
Jing, Xinli [1 ,2 ]
机构
[1] Xi An Jiao Tong Univ, Dept Appl Chem, Sch Sci, Xian 710049, Shaanxi, Peoples R China
[2] MOE Key Lab Nonequilibrium Synth & Modulat Conden, Xian 710049, Shaanxi, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
Phenolic resin; Pyrolysis mechanism; Thermal properties; Phenylborates; Boron oxide; MOLECULAR-DYNAMICS SIMULATION; FORMALDEHYDE RESIN; CARBON/CARBON COMPOSITES; ABLATION PROPERTIES; RAMAN-SPECTROSCOPY; BISPHENOL-A; BORON; CARBON; STABILITY; MICROSTRUCTURE;
D O I
10.1016/j.polymdegradstab.2017.08.034
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study, phenolic resin (PR) that is modified with poly (dihydroxybiphenyl borate) (PDDB) is prepared. The chemical structure, thermal properties and structural evolution at high temperatures for cured PDDB/PR are investigated to understand the reason for high char yields. The results show that the phenylborates that are formed during curing are attributed to the high char yield of PDDB/PR (74%, 800 degrees C). Phenylborates can block parts of phenolic hydroxyl and effectively inhibit their thermal decomposition reaction. By tracking the resin residue and volatiles that are released during pyrolysis, it is determined that boron oxide and boron carbide are formed via pyrolysis and help reduce carbon loss. Introducing PDDB into PR improves the graphitization degree and graphite crystallites of carbonization products, which promotes the formation of ordered glassy carbon during pyrolysis. Additionally, the CF/PDDB/PR composites show excellent mechanical and ablation properties due to good interfacial adhesion between resin matrix and fibreThis method makes it possible for using PDDB to enhance the thermal properties of the polymer with lower cost, more functions and broader applications. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:378 / 391
页数:14
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