Structure-property relationships of new polystyrene nanocomposites prepared from initiator-containing layered double hydroxides of zinc aluminum and magnesium aluminum

被引:37
作者
Manzi-Nshuti, Charles [1 ,2 ]
Chen, Dan [3 ]
Su, Shengpei [3 ]
Wilkie, Charles A. [1 ,2 ]
机构
[1] Marquette Univ, Dept Chem, Milwaukee, WI 53201 USA
[2] Marquette Univ, Fire Retardant Res Facil, Milwaukee, WI 53201 USA
[3] Hunan Normal Univ, Coll Chem & Chem Engn, Changsha 410081, Hunan, Peoples R China
关键词
Nanocomposites; Layered double hydroxides; Fire retardancy; Polystyrene; GLASS-TRANSITION BEHAVIOR; POLYMER; NANOPARTICLES; POLYETHYLENE; SIZE;
D O I
10.1016/j.polymdegradstab.2009.03.021
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polystyrene/layered double hydroxides (PS/LDHs) nanocomposites were prepared by free radical polymerization of styrene monomer in the presence of LDHs intercalated with 4,4'-azobis(4-cyanopentanoate) anions (LDH-ACPA). XRD and ATR-IR are used to confirm that the materials produced are layered and the presence of the azo-initiator anions in these LDHs. These LDHs were used successfully to polymerize styrene and both XRD and TEM images of the composites support the formation of a mixed exfoliated-intercalated nanocomposite for ZnAl-ACPA but a microcomposite for MgAI-ACPA. The magnesium-containing LDHs decreased the glass transition temperature (T-g) of the composites while ZnAl-ACPA did not affect T-g significantly. The T-g depression is related to enhanced polymer dynamics due to the extra free volume at the LDH additive-polymer interface. A reduction in the onset of thermal decomposition temperature was observed in PS/LDH compared to neat PS, likely due to the early decomposition of the LDH. The fire performance, as evaluated by the cone calorimeter, reveal that PS-ZnAl-ACPA shows enhanced fire properties compared to PS-MgAl-ACPA. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1290 / 1297
页数:8
相关论文
共 39 条
[1]   Synthesis of Al-rich hydrotalcite-like compounds by using the urea hydrolysis reaction-control of size and morphology [J].
Adachi-Pagano, M ;
Forano, C ;
Besse, JP .
JOURNAL OF MATERIALS CHEMISTRY, 2003, 13 (08) :1988-1993
[2]   Glass transition behavior of alumina/polymethylmethacrylate nanocomposites [J].
Ash, BJ ;
Schadler, LS ;
Siegel, RW .
MATERIALS LETTERS, 2002, 55 (1-2) :83-87
[3]   HEAT RELEASE RATE - THE SINGLE MOST IMPORTANT VARIABLE IN FIRE HAZARD [J].
BABRAUSKAS, V ;
PEACOCK, RD .
FIRE SAFETY JOURNAL, 1992, 18 (03) :255-272
[4]   Preparation and characterization of poly(vinyl chloride)/layered double hydroxides nanocomposite via in situ suspension polymerization [J].
Bao, Yong-Zhong ;
Huang, Zhi-Ming ;
Weng, Zhi-Xue .
JOURNAL OF APPLIED POLYMER SCIENCE, 2006, 102 (02) :1471-1477
[5]  
Bellamy L.J., 1975, The Infra-Red Spectra of Complex Molecules, VVolume 1, P294
[6]   Preparation and properties of nano-Al2O3 particles/polyester/epoxy resin ternary composites [J].
Cao, YM ;
Sun, J ;
Yu, DH .
JOURNAL OF APPLIED POLYMER SCIENCE, 2002, 83 (01) :70-77
[7]  
Caseri W, 2000, MACROMOL RAPID COMM, V21, P705, DOI 10.1002/1521-3927(20000701)21:11<705::AID-MARC705>3.0.CO
[8]  
2-3
[9]  
Cheikhalard T, 1998, ANGEW MAKROMOL CHEM, V256, P49
[10]   New nanocomposites constituted of polyethylene and organically modified ZnAl-hydrotalcites [J].
Costantino, U ;
Gallipoli, A ;
Nocchetti, M ;
Camino, G ;
Bellucci, F ;
Frache, A .
POLYMER DEGRADATION AND STABILITY, 2005, 90 (03) :586-590