Somayeh Mohammadi, Martin G. Bouldo, Mojtaba Enayati
{"title":"FeCl3-Doped Cobalt Ferrite as an Efficient Magnetic Catalyst for PET Glycolysis Depolymerization","authors":"Somayeh Mohammadi, Martin G. Bouldo, Mojtaba Enayati","doi":"10.1007/s10924-024-03341-2","DOIUrl":null,"url":null,"abstract":"<div><p>A comparative study of cobalt ferrite (CoFe<sub>2</sub>O<sub>4</sub>) catalysts synthesized via three different methods is presented, aiming to evaluate their catalytic activities in poly(ethylene terephthalate) (PET) chemical depolymerization by glycolysis. The synthesized catalysts have been characterized by X-ray photoelectron spectroscopy, X-ray diffraction, X-ray fluorescence, scanning electron microscopy, and energy dispersive spectroscopy. The conversion of PET into bis(2-hydroxyethyl)terephthalate (BHET) monomer was examined using these cobalt ferrites. The BHET in the reaction mixture was analyzed by FTIR, HPLC, DSC, and TGA and results show the catalyst synthesized by coprecipitation demonstrates the highest BHET yield (95.4%) at a temperature of 200 °C and a pressure of 0.7 bar in 1 h with only 1.0 wt% loading. Hydrothermal synthesized CoFe<sub>2</sub>O<sub>4</sub> and solvent-free synthesized CoFe<sub>2</sub>O<sub>4</sub> both showed lower BHET yields. The catalytic performance of the coprecipitated CoFe<sub>2</sub>O<sub>4</sub> catalyst was influenced by the presence of unintentionally trapped FeCl<sub>3</sub> within the catalyst, which resulted in its enhanced activity. The CoFe<sub>2</sub>O<sub>4</sub> catalyst from coprecipitation exhibited acceptable magnetic recoverability and reusability for four consecutive cycles, further highlighting its usefulness and sustainability.</p><h3>Graphical Abstract</h3><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":659,"journal":{"name":"Journal of Polymers and the Environment","volume":"32 11","pages":"5738 - 5749"},"PeriodicalIF":4.7000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Polymers and the Environment","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s10924-024-03341-2","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
A comparative study of cobalt ferrite (CoFe2O4) catalysts synthesized via three different methods is presented, aiming to evaluate their catalytic activities in poly(ethylene terephthalate) (PET) chemical depolymerization by glycolysis. The synthesized catalysts have been characterized by X-ray photoelectron spectroscopy, X-ray diffraction, X-ray fluorescence, scanning electron microscopy, and energy dispersive spectroscopy. The conversion of PET into bis(2-hydroxyethyl)terephthalate (BHET) monomer was examined using these cobalt ferrites. The BHET in the reaction mixture was analyzed by FTIR, HPLC, DSC, and TGA and results show the catalyst synthesized by coprecipitation demonstrates the highest BHET yield (95.4%) at a temperature of 200 °C and a pressure of 0.7 bar in 1 h with only 1.0 wt% loading. Hydrothermal synthesized CoFe2O4 and solvent-free synthesized CoFe2O4 both showed lower BHET yields. The catalytic performance of the coprecipitated CoFe2O4 catalyst was influenced by the presence of unintentionally trapped FeCl3 within the catalyst, which resulted in its enhanced activity. The CoFe2O4 catalyst from coprecipitation exhibited acceptable magnetic recoverability and reusability for four consecutive cycles, further highlighting its usefulness and sustainability.
期刊介绍:
The Journal of Polymers and the Environment fills the need for an international forum in this diverse and rapidly expanding field. The journal serves a crucial role for the publication of information from a wide range of disciplines and is a central outlet for the publication of high-quality peer-reviewed original papers, review articles and short communications. The journal is intentionally interdisciplinary in regard to contributions and covers the following subjects - polymers, environmentally degradable polymers, and degradation pathways: biological, photochemical, oxidative and hydrolytic; new environmental materials: derived by chemical and biosynthetic routes; environmental blends and composites; developments in processing and reactive processing of environmental polymers; characterization of environmental materials: mechanical, physical, thermal, rheological, morphological, and others; recyclable polymers and plastics recycling environmental testing: in-laboratory simulations, outdoor exposures, and standardization of methodologies; environmental fate: end products and intermediates of biodegradation; microbiology and enzymology of polymer biodegradation; solid-waste management and public legislation specific to environmental polymers; and other related topics.