Efficient degradation of polystyrene microplastic pollutants in soil by dielectric barrier discharge plasma.

In this study, the atmospheric dielectric barrier discharge (DBD) plasma was proposed for the degradation of polystyrene microplastics (PS-MPs) for the first time, due to its ability to generate reactive oxygen species (ROS). The local temperature in plasma was found to play a crucial role, as it enhanced the degradation reaction induced by ROS when it exceeded the melting temperature of PS-MPs. Factors including applied voltage, air flow rate, and PS-MPs concentration were investigated, and the degradation products were analyzed. High plasma energy and adequate supply of ROS were pivotal in promoting degradation. At 20.1 kV, the degradation efficiency of PS-MPs reached 98.7% after 60 min treatment, with gases (mainly COx, accounting for 96.4%) as the main degradation products. At a concentration of 1 wt%, the PS-MPs exhibited a remarkable conversion rate of 90.6% to COx, showcasing the degradation performance and oxidation degree of this technology. Finally, the degradation mechanism of PS-MPs combined with the detection results of ROS was suggested. This work demonstrates that DBD plasma is a promising strategy for PS-MPs degradation, with high energy efficiency (8.80 mg/kJ) and degradation performance (98.7% within 1 h), providing direct evidence for the rapid and comprehensive treatment of MP pollutants.

Mass concentration and distribution characteristics of microplastics in landfill mineralized refuse using efficient quantitative detection based on Py-GC/MS.

Landfilling is the most traditional disposal method of domestic waste. Plastic waste in landfill sites could degrade to microplastics (MPs) and diffuse to the surrounding environment with leachate. However, MPs pollution in landfill mineralized refuse has not been well recognized. In the present research, a detection method for mixed MPs of polyethylene (PE), polypropylene (PP), and polystyrene (PS) based on Py-GC/MS was established and verified. The method is suitable for the rapid quantitative detection of large-batch of complex solid matrix samples, with an average deviation of less than 10%. Based on the method, samples from a landfill site in South China were studied, where PE was found to be the main component. The total concentration of MPs in mineralized refuse was 7.62 kg/t in the old area and 5.49 kg/t in the young area. Further analysis showed that the content of MPs was correlated with that of plastic waste and the landfill age, indicating that a considerable proportion was secondary MPs. The reserves of MPs in landfill sites may have reached an alarming number. In the absence of adequate safeguards, quantities of MPs may spread from the landfill sites, resulting in serious pollution of the surrounding soil and groundwater.

Dechlorination of waste polyvinyl chloride (PVC) through non-thermal plasma.

Dechlorination is essential for the chemical recycling of waste polyvinyl chloride (PVC) plastics. This study investigated the use of non-thermal plasma (NTP) for chlorine removal, with a focus on the effects of treatment time and discharge power on dechlorination efficiency. The results showed that longer treatment times and higher discharge powers led to better dechlorination performance. The maximum efficiency (98.25%) and HCl recovery yield (55.72%) were achieved at 180 W power after 40 min of treatment where 96.44% of Cl existed in the form of HCl gas, 1.44% in the liquid product, and 2.12% in the solid residue product. NTP at a discharge power of 150 W showed better dechlorination performance compared to traditional thermal pyrolysis treatment in temperatures ranging from 200 to 400 °C. The activation energy analysis of the chlorine removal showed that compared to pyrolysis-based dechlorination (137.09 kJ/mol), NTP-based dechlorination (23.62 kJ/mol) was more easily achievable. This work presents a practical method for the dechlorination of waste PVC plastic using a novel technology without requiring additional thermal and pressure input.

Dechlorination and fuel gas generation in chemical looping conversion of waste PVC over inherently Na/Ca/K-containing bauxite residue-based oxygen carriers.

The inert atmosphere in chemical looping (CL) technology can considerably inhibit the formation of polychlorinated dibenzo-p-dioxins and dibenzofurans during the thermal treatment of polyvinyl chloride plastic (PVC) waste. In this study, PVC was innovatively converted to dechlorinated fuel gas via CL gasification under a high reaction temperature (RT) and the inert atmosphere by applying an unmodified bauxite residue (BR) as both a dechlorination agent and oxygen carrier. The dechlorination efficiency reached 49.98% at an oxygen ratio of only 0.1. Furthermore, a moderate RT (750 °C in this study) and an increased oxygen ratio enhanced the dechlorination effect. The highest dechlorination efficiency (92.12%) was achieved at an oxygen ratio of 0.6. Iron oxides in BR improved the generation of syngas from CL reactions. The yields of the effective gases (CH4, H2, and CO) increased by 57.13% to 0.121 Nm3/kg with an increase in oxygen ratio from 0 to 0.6. A high RT improved the production of the effective gases (an 809.39% increase to 0.344 Nm3/kg from 600 to 900 °C). Energy-dispersive spectroscopy and X-ray diffraction were used to study the mechanism, and formation of NaCl and Fe3O4 was observed on the reacted BR, indicating the successful adsorption of Cl and its capability as an oxygen carrier. Therefore, BR eliminated Cl in situ and enhanced the generation of value-added syngas, thereby achieving efficient PVC conversion.

Dielectric barrier discharge plasma for the remediation of microplastic-contaminated soil from landfill.

The huge amount of plastic waste accumulated in landfills has caused serious microplastic (MP) pollution to the soil environment, which has become an urgent issue in recent years. It is challenging to deal with the non-biodegradable MP pollutants in actual soil from landfills. In this study, a coaxial dielectric barrier discharge (DBD) system was proposed to remediate actual MP-contaminated landfill soil due to its strong oxidation capacity. The influence of carrier gas type, applied voltage, and air flow rate was investigated, and the possible degradation pathways of MP pollutants were suggested. Results showed the landfill soil samples contained four common MP pollutants, including polyethylene (PE), polypropylene (PP), polystyrene (PS), and polyvinyl chloride (PVC) with sizes ranging from 50 to 1500 µm. The MP pollutants in the soil were rapidly removed under the action of reactive oxygen species (ROS) generated by DBD plasma. Under the air flow rate of 1500 mL min-1, the maximum remediation efficiency represented by mass loss reached 96.5% after 30 min treatment. Compared with nitrogen, when air was used as the carrier gas, the remediation efficiency increased from 41.4% to 81.6%. The increased applied voltage from 17.5 to 24.1 kV could also promote the removal of MP contaminants. Sufficient air supply was conducive to thorough removal. However, when the air flow rate reached 1500 mL min-1 and continued to rise, the final remediation efficiency would be reduced due to the shortened residence time of ROS. The DBD plasma treatment proposed in this study showed high energy efficiency (19.03 mg kJ-1) and remediation performance (96.5%). The results are instructive for solving MP pollution in the soil environment.

BTEX recovery from waste rubbers by catalytic pyrolysis over Zn loaded tire derived char.

Recovering valuable chemicals (BTEX: Benzene, toluene, ethylbenzene, and xylene) via catalytic pyrolysis of waste tires is a promising and sustainable approach. Zinc loaded tire derived char (TDC) was used as cheap catalyst for recovering valuable BTEX products from waste tire through pyrolysis in this study. The catalytic capability of TDC on BTEX production were experimentally investigated with respect to Zn content, catalytic temperature, and catalyst-to-tire ratio. Due to the abundant acid sites on the surface, the TDC showed notable catalytic capability for improving BTEX yield which was 2.4 times higher than that from uncatalyzed case. The loading of additional Zn increased the acid sites on the TDC and the catalytic performance was further improved. The increase of catalytic temperature and catalyst-to-tire ratio favored the formation of BTEX, but it also brought undesirable consequences, such as the mass loss of tire pyrolysis oil (TPO) and the formation of polycyclic aromatic hydrocarbons. The optimal TPO products were obtained at 600 °C with catalyst-to-tire ratio of 20. At this condition, the relative content of BTEX reached 54.70% and the cumulative BTEX yield was 10.13 wt%, increasing by 5.95 times compared to that of non-catalytic condition. This work provided a novel strategy of replacing traditional expensive catalysts with low-cost and effective carbon-based materials in the field of catalytic pyrolysis of waste tires.