Fractionated degradation and valorization of polypropylene waste into sulfonate surfactants

Tandem upcycling presents a promising approach to converting plastic waste into valuable chemicals. Controlling the chain length distribution (CLD) of hydrocarbons in plastic degradation is crucial for the downstream synthesis of high-quality and high-value functional chemicals. However, controlling the CLD remains a significant challenge due to the high randomness and poor regulation of polymer chain scission. Herein, we introduce a fractionated degradation approach to tune the CLD of hydrocarbons derived from polypropylene (PP) degradation, thereby facilitating effective downstream valorization. By designing a fractionated degradation reactor that manipulates latent heat, we achieve size-selective degradation of PP into C<sub>6</sub>-C<sub>15</sub> and C<sub>15</sub>-C<sub>28</sub> α-alkenes with narrower and more tunable CLDs compared to traditional methods. Modeling and ASPEN simulations reveal a quasi-linear relationship between chain length and fraction temperatures, as well as a positive correlation between CLD and number of fractions. Scale-up experiments with 10 kg of real-life PP waste validate the effectiveness of the fractionated degradation. The PP-derived α-alkenes with narrow CLDs exhibit superior performance in sulfonation, resulting in foaming, detergency, and biodegradability, comparable to commercial sulfonate surfactants. Techno-economic and life cycle analyses demonstrate improved economic and ecological benefits of PP-to-surfactant upcycling over existing petrochemical-based methods.

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Journal
Nature Communications
Published
2025-11-25
DOI
https://doi.org/10.1038/s41467-025-66592-0
Primary Topic
Microplastics and Plastic Pollution
Type
article
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article

Fractionated degradation and valorization of polypropylene waste into sulfonate surfactants

Zhen Xu, Fuping Pan, Qikun Zhang, Kai‐Jie Chen et al.
Nature Communications
Microplastics and Plastic Pollution
article

Fractionated degradation and valorization of polypropylene waste into sulfonate surfactants

Zhen Xu, Fuping Pan, Qikun Zhang, Kai‐Jie Chen, Tao Wang, Meiling Chen, Yang Zhang, Rong Yang, Feng Liu, Hao Sun, Jianjun Xu
article en

Abstract

Tandem upcycling presents a promising approach to converting plastic waste into valuable chemicals. Controlling the chain length distribution (CLD) of hydrocarbons in plastic degradation is crucial for the downstream synthesis of high-quality and high-value functional chemicals. However, controlling the CLD remains a significant challenge due to the high randomness and poor regulation of polymer chain scission. Herein, we introduce a fractionated degradation approach to tune the CLD of hydrocarbons derived from polypropylene (PP) degradation, thereby facilitating effective downstream valorization. By designing a fractionated degradation reactor that manipulates latent heat, we achieve size-selective degradation of PP into C<sub>6</sub>-C<sub>15</sub> and C<sub>15</sub>-C<sub>28</sub> α-alkenes with narrower and more tunable CLDs compared to traditional methods. Modeling and ASPEN simulations reveal a quasi-linear relationship between chain length and fraction temperatures, as well as a positive correlation between CLD and number of fractions. Scale-up experiments with 10 kg of real-life PP waste validate the effectiveness of the fractionated degradation. The PP-derived α-alkenes with narrow CLDs exhibit superior performance in sulfonation, resulting in foaming, detergency, and biodegradability, comparable to commercial sulfonate surfactants. Techno-economic and life cycle analyses demonstrate improved economic and ecological benefits of PP-to-surfactant upcycling over existing petrochemical-based methods.

Nature CommunicationsVol. 16(1)
Tongji University (CN), Dongbei University of Finance and Economics (CN), Northwestern Polytechnical University (CN), Shandong Normal University (CN), Ministry of Education (ME), Northwestern Polytechnic University (US)
Openalex Percentile: Top 70%
Microplastics and Plastic Pollution
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