Effects of pressure on the degradation of poly(vinyl chloride)

被引:14
作者
Kamo, T [1 ]
Kodera, Y [1 ]
Sato, Y [1 ]
Kushiyama, S [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Inst Energy Utilizat, Tsukuba, Ibaraki 3058569, Japan
关键词
PVC; pressure dependence; reaction mechanism; paraffin;
D O I
10.1016/j.polymdegradstab.2003.09.014
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(vinyl chloride) was decomposed for 0-90 min at 300-440 degreesC under 0-6.0 MPa of nitrogen pressure. Hydrogen chloride, liquid products, and residue were the main decomposition products. The yield or liquid products decreased with increasing reaction pressure. whereas the yield of residue increased, reaching maxima at 9.8 MPa (400 degreesC) and 22.4 MPa (440 degreesC). The pressure dependences of the product distribution and atomic ratio of hydrogen to carbon (H/C) imply that some of the liquid products were polycondensed with the dehydrochlorinated PVC and were retained in the residue under high-pressure. At atmospheric pressure, benzene was the predominant product. The yield of benzene decreased sharply with pressure, whereas the yield of linear paraffins increased significantly. The liquid product distribution suggests that polyene chains in the dehydrochlorinated PVC were converted to benzene and alkylbenzene under atmospheric pressure. However, some of the polyene chains underwent hydrogenation to form linear paraffins under high pressure. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:79 / 85
页数:7
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