Nakatani Hisayuki, Ohshima Yuina, Uchiyama Taishi, Motokucho Suguru
Polymeri Materials Laboratory, Chemistry and Materials Program, Nagasaki University, 1-14 Bunkyo-Machi, Nagasaki, 852-8521, Japan.
Sci Rep. 2022 Nov 2;12(1):18501. doi: 10.1038/s41598-022-23435-y.
The polystyrene (PS) retrieved from the beach exhibited no change in surface texture. In contrast to it, the retrieved polypropylene (PP) had a rumpled surface texture. Highly reactive sulfate radical generated by KSO was employed as degradation initiator of PP and PS, and their degradation behavior was studied in water. The PS carbonyl index value gradually went up down, and its molecular weight (MW) curve discontinuously shifted to a lower MW with the increase of the degradation time unlike the PP. It was found that the PP microplastic production rate was approximately three time higher than the PS from weight ratio dependence on degradation time. The higher microplastic production rate of PP arose from its crystallizability. The voids were produced by change in specific volume occurring by chemi-crystallization and then provoked the cracks leading to quick fragmentation. The SEM photographs suggested that the PP microplastic size facilely reached nm order by the cracking around lamella.
从海滩回收的聚苯乙烯(PS)表面纹理没有变化。与之形成对比的是,回收的聚丙烯(PP)表面有褶皱纹理。用KSO产生的高活性硫酸根自由基作为PP和PS的降解引发剂,并在水中研究了它们的降解行为。与PP不同,PS的羰基指数值逐渐下降,其分子量(MW)曲线随着降解时间的增加而不连续地向较低的MW移动。从降解时间的重量比依赖性发现,PP微塑料的产生率大约比PS高两倍。PP较高的微塑料产生率源于其结晶性。化学结晶引起的比容变化产生了空隙,进而引发裂缝导致快速破碎。扫描电子显微镜照片表明,PP微塑料尺寸通过片晶周围的开裂很容易达到纳米级。