Stability of organically modified montmorillonites and their polystyrene nanocomposites after prolonged thermal treatment

被引:17
作者
Frankowski, David J.
Capracotta, Michael D.
Martin, James D.
Khan, Saad A.
Spontak, Richard J. [1 ]
机构
[1] N Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
[2] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
[3] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
[4] N Carolina State Univ, Dept Mat Sci & Engn, Raleigh, NC 27695 USA
关键词
D O I
10.1021/cm061953k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Melt intercalation of montmorillonite (MMT) into polymeric matrices to improve the mechanical properties of polymers has evolved into a subject of tremendous fundamental and technological interest. The thermal treatment experienced during processing or end use can substantially affect the clay and diminish the target properties of polymer/clay nanocomposites (NCs) because of deintercalation or degradation of surface modifiers. In this work, changes in morphology, chemistry, and thermal stability of organically modified (OM) MMT after annealing in O-2-rich and N-2 environments are investigated. Degradation of the alkyl ammonium cation occurs at temperatures as low as 105 degrees C upon prolonged exposure in an O-2-rich environment. X-ray diffractometry (XRD) performed in situ establishes the response of two OM-MMTs to elevated temperatures at short times, whereas ex situ XRD provides insight into high-temperature exposure at long times. Active sites on the silicate surfaces are found to induce scission of, as well as chemical interaction with, the chains comprising a polystyrene (PS) matrix. Size-exclusion chromatography indicates that PS chain scission occurs primarily after relatively short annealing times, whereas branching and cross-linking are more prevalent after long exposure times in an O-2-rich environment.
引用
收藏
页码:2757 / 2767
页数:11
相关论文
共 71 条
[1]  
[Anonymous], 1999, LANGES HDB CHEM, V15
[2]   3D Hierarchical orientation in polymer-clay nanocomposite films [J].
Bafna, A ;
Beaucage, G ;
Mirabella, F ;
Mehta, S .
POLYMER, 2003, 44 (04) :1103-1115
[3]   Kinetic analysis of the thermal degradation of polystyrene-montmorillonite nanocomposite [J].
Bourbigot, S ;
Gilman, JW ;
Wilkie, CA .
POLYMER DEGRADATION AND STABILITY, 2004, 84 (03) :483-492
[4]  
Cheng GL, 2000, MACROMOL RAPID COMM, V21, P846, DOI 10.1002/1521-3927(20000801)21:12<846::AID-MARC846>3.0.CO
[5]  
2-E
[6]   Thermal decomposition of alkyl ammonium ions and its effects on surface polarity of organically treated nanoclay [J].
Dharaiya, D ;
Jana, SC .
POLYMER, 2005, 46 (23) :10139-10147
[7]   Thermal stability analysis of organo-silicates, using solid phase microextraction techniques [J].
Edwards, G ;
Halley, P ;
Kerven, G ;
Martin, D .
THERMOCHIMICA ACTA, 2005, 429 (01) :13-18
[8]   Generation of electrospun fibers of nylon 6 and nylon 6-montmorillonite nanocomposite [J].
Fong, H ;
Liu, WD ;
Wang, CS ;
Vaia, RA .
POLYMER, 2002, 43 (03) :775-780
[9]   Polymer matrix degradation and color formation in melt processed nylon 6/clay nanocomposites [J].
Fornes, TD ;
Yoon, PJ ;
Paul, DR .
POLYMER, 2003, 44 (24) :7545-7556
[10]  
FRANKOWSKI DJ, UNPUB