The impact of two different fullerenes (C-60 and PCBM) on the thermal stability of the corresponding polystyrene (PS) fullerene composites was studied over the whole composition range, under nitrogen (N-2) and air atmospheres using dynamic thermogravimetric analysis (TGA). The aim of this study was to compare the thermal stabilization effect of C-60 and PCBM on polystyrene. Both in nitrogen and in air, all the composites are more stable to thermal decomposition than the pure PS. While in nitrogen the thermal degradation of the PS-fullerene composites occurs in a single step process, in air it occurs in a two-step process in which the first step consists mainly of the degradation of PS, and the second step consists mainly of the fullerene degradation. TGA can be used successfully to determine the amount of C-60 and PCBM in the PS composites over the whole composition range. In nitrogen, the residual mass values obtained above 450 degrees C correlate linearly with the initial amounts of fullerene present in the composites. In air, the residual mass values observed at the temperatures of transition from the first to the second decomposition step also correlate linearly with the initial amounts of fullerene present in the composites. In nitrogen, the thermal stabilization effects of C-60 and PCBM are very similar. Conversely, in air PCBM shows a higher thermal stabilization effect than C-60 for identical fullerene loadings. We suggest that the improved thermo-oxidative stability of the PCBM composites compared to the C-60 composites is due to the fact that, as previously reported in the literature, PCBM disperses better in a PS matrix than C-60. (C) 2014 Elsevier Ltd. All rights reserved.
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Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Wan, Dong
Xing, Haiping
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Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Xing, Haiping
Liu, Feng
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Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Liu, Feng
Wang, Lu
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Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Wang, Lu
Wang, Yujie
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Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Wang, Yujie
Tan, Haiying
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Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Tan, Haiying
Jiang, Zhiwei
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Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
Jiang, Zhiwei
Tang, Tao
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Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R ChinaChinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China