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
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