The role of NaOH in the hydrothermal dehydrochlorination of polyvinyl chloride

被引:11
|
作者
Hungwe, Douglas [1 ]
Hosokawa, Satomi [1 ]
Xu, Hao [2 ]
Yamasaki, Yuki [3 ]
机构
[1] Hosei Univ, Res & Dev Ctr, 4342 Aiharamachi, Tokyo 1940298, Japan
[2] Tokyo Inst Technol, Dept Transdisciplinary Sci & Engn, G5-8,4259 Nagatsuta, Yokohama 2268502, Japan
[3] Hosei Univ, Dept Econ, 4342 Aiharamachi, Tokyo 1940298, Japan
关键词
Hydrothermal dechlorination; Polyvinyl chloride; Activation energy; Reaction rate; THERMAL DEHYDROCHLORINATION; POLY(VINYL CHLORIDE); HYDRATION FORCES; MICA SURFACES; DECHLORINATION; DEGRADATION; PVC; AUTOCATALYSIS; MECHANISM;
D O I
10.1016/j.polymdegradstab.2023.110266
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The role of NaOH in polyvinyl chloride (PVC) dehydrochlorination was studied over a concentration range that yielded the maximum reaction rate. In addition to limiting autocatalysis through HCl scavenging, NaOH also influences the physicochemical evolution of PVC during hydrothermal treatment. In 3 M NaOH, the dechlorination rate peaked because NaOH effectively prevented particle agglomeration and autocatalysis. This is attributed to the action of sodium cations in producing short-range hydration repulsive forces that prevent the adhesion of particles and facilitate significant size reduction. The apparent activation energy was 138 +/- 3.0 kJmol(-1). In 2 M NaOH, particle agglomeration and pronounced autocatalysis reduced the activation energy to 105 +/- 7.2 kJmol(-1). Therefore, NaOH influences both the morphological evolution and dechlorination reaction kinetics.
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页数:6
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