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Cited by 261

The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.

Microwave-Induced Pyrolysis of Plastic Wastes

Ludlow-Palafox, Carlos, Chase, Howard A.·2001·Industrial & Engineering Chemistry Research

Abstract

The performance of a novel microwave-induced pyrolysis process was evaluated by studying the degradation of high-density polyethylene and aluminum/polymer laminates in a semibatch bench-scale apparatus. The results showed that the new process has the same general features as other, more traditional, pyrolytic processes but with the advantage that it is able to deal with problematic wastes such as laminates. Degradation experiments were performed between 500 and 700 °C and the relationship between temperature, residence time of the pyrolytic products in the reactor, and the chemical composition of the hydrocarbon fraction produced was investigated. Toothpaste tubing was used as an example of a laminated material to be treated with the novel process. Clean aluminum was recovered together with hydrocarbons and the trial proved that the process has excellent potential for the treatment of plastic wastes on a commercial scale.

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Metadata

Authors
Ludlow-Palafox, C., & Chase, H. A.
Venue
Industrial & Engineering Chemistry Research
Published
2001-10-01
Volume
40
Issue
22
Pages
4749-4756
ISSN
  • 0888-5885 (ISSN-L)
  • 1520-5045
OpenAlex
W2055493903
Cited by
261
References
11
FWCI
2.47
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Microwave-Induced Pyrolysis of Plastic Wastes. https://app.cochat.ai/papers/10.1021/ie010202j
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Ludlow-Palafox, C., & Chase, H. A. (2001). Microwave-Induced Pyrolysis of Plastic Wastes. Industrial & Engineering Chemistry Research. https://doi.org/10.1021/ie010202j

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.