{"title":"通过硝酸氧化法对聚苯乙烯树脂及其一次性使用产品进行化学回收:其他塑料污染的机理和影响","authors":"Kusuma Pinsuwan , Naritsara Phowattanachai , Purimpraj Kaewnoparat , Arachaporn Malakul Na Ayutthaya , Tanawat Poungboon , Pakorn Opaprakasit , Atitsa Petchsuk , Mantana Opaprakasit","doi":"10.1016/j.polymer.2024.127888","DOIUrl":null,"url":null,"abstract":"<div><div>Polystyrene (PS) is a widely used plastic, especially in single-use items, leading to a large accumulation of waste and serious environmental problems. A promising solution to this is an advanced recycling process to circularly use the material. In this study, the chemical recycling of PS resin (GP110) and commercial PS products <em>via</em> nitric acid oxidation is investigated. In addition, the effects of HDPE, PP, and PVC as contaminants in PS on the reaction mechanisms and product compositions are examined. Small-scaled reactions at 150–190 °C in a 50 mL hydrothermal autoclave revealed that GP110 is oxidized and mostly converted to benzoic acid (BA), 4-nitrobenzoic acid (4NB), and 3-nitrobenzoic acid (3NB) with a reaction time shorter than 8 h. The conversion of BA to 3NB is more favorable at high temperatures. The reactions at 170 °C for 4 h on commercial PS products, <em>i.e.</em>, spoons, boxes, and cups, led to a much lower carbon recovery (∼24–29 %) than GP110 resin (∼42 %). A reaction time shorter than 4 h is required to reduce carbon loss, as these products are fabricated from lower molar mass PS. The oxidation of S<sub>B</sub> as a model PS waste in a larger scaled reaction, <em>i.e.</em>, a 250 mL hydrothermal reactor, is used to assess the feasibility of applying the process for chemical recycling of PS waste. The processes (at 170 and 180 °C for 3 h) provided 53–80 % carbon recovery. The suitable ratios of solid to aqueous solution (0.23 g/mL nitric) and PS to nitric acid are in the range of ∼1/12 to 1/16 g/mL and 1/2.8 to 1/4.2 g/g, respectively, depending on the reaction conditions and the pressure limitation of the reactor. Concerning PS waste contaminated with other plastics, the results suggest that contamination with PP should be avoided in depolymerizing PS, as this can cause adverse effects, especially excessively built-up pressure in the system due to the generation of excess gaseous products.</div></div>","PeriodicalId":405,"journal":{"name":"Polymer","volume":"316 ","pages":"Article 127888"},"PeriodicalIF":4.1000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Chemical recycling of polystyrene resin and its single-used products via nitric acid oxidation: Mechanisms and effects of other plastic contaminations\",\"authors\":\"Kusuma Pinsuwan , Naritsara Phowattanachai , Purimpraj Kaewnoparat , Arachaporn Malakul Na Ayutthaya , Tanawat Poungboon , Pakorn Opaprakasit , Atitsa Petchsuk , Mantana Opaprakasit\",\"doi\":\"10.1016/j.polymer.2024.127888\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Polystyrene (PS) is a widely used plastic, especially in single-use items, leading to a large accumulation of waste and serious environmental problems. A promising solution to this is an advanced recycling process to circularly use the material. In this study, the chemical recycling of PS resin (GP110) and commercial PS products <em>via</em> nitric acid oxidation is investigated. In addition, the effects of HDPE, PP, and PVC as contaminants in PS on the reaction mechanisms and product compositions are examined. Small-scaled reactions at 150–190 °C in a 50 mL hydrothermal autoclave revealed that GP110 is oxidized and mostly converted to benzoic acid (BA), 4-nitrobenzoic acid (4NB), and 3-nitrobenzoic acid (3NB) with a reaction time shorter than 8 h. The conversion of BA to 3NB is more favorable at high temperatures. The reactions at 170 °C for 4 h on commercial PS products, <em>i.e.</em>, spoons, boxes, and cups, led to a much lower carbon recovery (∼24–29 %) than GP110 resin (∼42 %). A reaction time shorter than 4 h is required to reduce carbon loss, as these products are fabricated from lower molar mass PS. The oxidation of S<sub>B</sub> as a model PS waste in a larger scaled reaction, <em>i.e.</em>, a 250 mL hydrothermal reactor, is used to assess the feasibility of applying the process for chemical recycling of PS waste. The processes (at 170 and 180 °C for 3 h) provided 53–80 % carbon recovery. The suitable ratios of solid to aqueous solution (0.23 g/mL nitric) and PS to nitric acid are in the range of ∼1/12 to 1/16 g/mL and 1/2.8 to 1/4.2 g/g, respectively, depending on the reaction conditions and the pressure limitation of the reactor. Concerning PS waste contaminated with other plastics, the results suggest that contamination with PP should be avoided in depolymerizing PS, as this can cause adverse effects, especially excessively built-up pressure in the system due to the generation of excess gaseous products.</div></div>\",\"PeriodicalId\":405,\"journal\":{\"name\":\"Polymer\",\"volume\":\"316 \",\"pages\":\"Article 127888\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2024-11-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0032386124012242\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032386124012242","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Chemical recycling of polystyrene resin and its single-used products via nitric acid oxidation: Mechanisms and effects of other plastic contaminations
Polystyrene (PS) is a widely used plastic, especially in single-use items, leading to a large accumulation of waste and serious environmental problems. A promising solution to this is an advanced recycling process to circularly use the material. In this study, the chemical recycling of PS resin (GP110) and commercial PS products via nitric acid oxidation is investigated. In addition, the effects of HDPE, PP, and PVC as contaminants in PS on the reaction mechanisms and product compositions are examined. Small-scaled reactions at 150–190 °C in a 50 mL hydrothermal autoclave revealed that GP110 is oxidized and mostly converted to benzoic acid (BA), 4-nitrobenzoic acid (4NB), and 3-nitrobenzoic acid (3NB) with a reaction time shorter than 8 h. The conversion of BA to 3NB is more favorable at high temperatures. The reactions at 170 °C for 4 h on commercial PS products, i.e., spoons, boxes, and cups, led to a much lower carbon recovery (∼24–29 %) than GP110 resin (∼42 %). A reaction time shorter than 4 h is required to reduce carbon loss, as these products are fabricated from lower molar mass PS. The oxidation of SB as a model PS waste in a larger scaled reaction, i.e., a 250 mL hydrothermal reactor, is used to assess the feasibility of applying the process for chemical recycling of PS waste. The processes (at 170 and 180 °C for 3 h) provided 53–80 % carbon recovery. The suitable ratios of solid to aqueous solution (0.23 g/mL nitric) and PS to nitric acid are in the range of ∼1/12 to 1/16 g/mL and 1/2.8 to 1/4.2 g/g, respectively, depending on the reaction conditions and the pressure limitation of the reactor. Concerning PS waste contaminated with other plastics, the results suggest that contamination with PP should be avoided in depolymerizing PS, as this can cause adverse effects, especially excessively built-up pressure in the system due to the generation of excess gaseous products.
期刊介绍:
Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics.
The main scope is covered but not limited to the following core areas:
Polymer Materials
Nanocomposites and hybrid nanomaterials
Polymer blends, films, fibres, networks and porous materials
Physical Characterization
Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films
Polymer Engineering
Advanced multiscale processing methods
Polymer Synthesis, Modification and Self-assembly
Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization
Technological Applications
Polymers for energy generation and storage
Polymer membranes for separation technology
Polymers for opto- and microelectronics.