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Abstract The global production and consumption of plastics has increased at an alarming rate over the last few decades. The accumulation of pervasive and persistent waste plastic has concomitantly increased in landfills and the environment. The societal, ecological, and economic problems of plastic waste/pollution demand immediate and decisive action. In 2015, only 9% of plastic waste was successfully recycled in the United States. The major current recycling processes focus on the mechanical recycling of plastic waste; however, even this process is limited by the sorting/pretreatment of plastic waste and degradation of plastics during the process. An alternative to mechanical processes is chemical recycling of plastic waste. Efficient chemical recycling would allow for the production of feedstocks for various uses including fuels and chemical feedstocks to replace petrochemicals. This review focuses on the most recent advances for the chemical recycling of three major polymers found in plastic waste: PET, PE, and PP. Commercial processes for recycling hydrolysable polymers like polyesters or polyamides, polyolefins, or mixed waste streams are also discussed.
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This content will become publicly available on April 7, 2026
Real‐Time Quantification of Polyethylene Crystallinity via In Situ Mid‐ and Near‐Infrared Correlation Spectroscopy: Melting and Dissolution
ABSTRACT Elucidating the crystalline‐amorphous interface during decrystallization processes in semi‐crystalline polyethylene (PE) is crucial for the advancement of polymer theory and plastic‐to‐plastic recycling technologies. In this study, we carried out an in‐depth investigation of PE thin films undergoing melting or dissolution using a temperature‐controlled liquid flow‐cell experimental setup which provided in situ mid‐infrared (MIR, 4000–700 cm−1) and near‐infrared (NIR, 6000–4000 cm−1) spectra in real time. The spectroscopic results yielded molecular‐level information regarding PE decrystallization and chain disentanglement via fundamental vibrations, combination bands, and overtones which were correlated using hetero‐spectral two‐dimensional correlation spectroscopy (2D‐COS). A quantitative procedure for the calculation of PE degree of crystallinity was developed to track transformations of crystalline domains during melting and dissolution. This semi‐empirical model achieved a strong linear correlation of at least +0.93 in four spectral regions: 750–700 cm−1, 1500–1400 cm−1, 3000–2800 cm−1, and 4400–4200 cm−1. This analysis revealed important spectral trends about the interfacial solvation environment during these processes. Lastly, the time evolution of the unraveling, terminal methyl (CH3) groups of PE cilia was examined in relation to the decrystallization mechanism of PE. The insights obtained from this study advance the fundamental understanding necessary for developing new depolymerization and dissolution‐precipitation recycling strategies.
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- PAR ID:
- 10581565
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Journal of Polymer Science
- ISSN:
- 2642-4150
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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