Transformation and kinetics of chlorine-containing products during pyrolysis of plastic wastes

Pyrolysis can not only effectively dispose of plastic wastes but also reclaim valuable chemicals and biochar. However, the production and release of second pollutants, particularly chlorine-containing products, have been neglected. The mechanism for the transformation of chlorine during the pyrolysis of plastic wastes remains unclear. Herein, a thermogravimetric Fourier transform infrared mass spectrometry technology was used to investigate the migration and transformation of substances during the pyrolysis of polyvinyl chloride (PVC) plastic from 200 degrees C to 900 degrees C with heating rates of 5, 50, 100, 150, and 200 K min(-1). Results show the first stage of weight loss is at 200 degrees C-360 degrees C, where the dehydrochlorination of PVC mainly occurred, accompanied by the formation of conjugated double bonds and a small number of hydrocarbon compounds. The second stage of weight loss is at 360 degrees C-550 degrees C, where the breakage and rearrangement of the long polyethene chain may occur. Kinetics analysis shows the higher activation energy value is in the second stage, which indicates that the second stage reaction is less likely to occur and the Flynn-Wall-Ozawa method is more suitable for the study of plastic pyrolysis kinetics. This study suggests that second pollutants can be minimized during controllable pyrolysis.

Automated summary

The study investigated the migration and transformation of substances during the pyrolysis of PVC plastics using a thermogravimetric Fourier transform infrared mass spectrometry technology. Results showed that dehydrochlorination of PVC mainly occurred in the first stage, accompanied by the formation of conjugated double bonds and a small number of hydrocarbon compounds. Furthermore, the study suggested that by controlling the pyrolysis process, the generation of second pollutants can be minimized.