In-Situ Catalytic Pyrolysis of Polystyrene with Sewage Sludge-Derived Catalysts: Sewage Sludge Ash, Sewage Sludge Char, and Fe-Impregnated Acid-Leached Sewage Sludge Char

Sewage sludge (SS)-derived materials were investigated as low-cost heterogeneous catalytic materials for polystyrene (PS) pyrolysis, focusing on the effects of thermal treatment, HCl leaching, and Fe impregnation. Sewage sludge ash (SSA), sewage sludge char (SSC), and HCl-leached Fe-impregnated sewage sludge char (Fe-LSSC) were evaluated as in-situ catalytic materials. Catalyst-to-PS ratios of 1:1–1:10 were investigated in a horizontal semi-batch tubular reactor operated in an in-situ catalyst–polymer contact mode at 800 °C. Thermal pyrolysis produced 63.9 wt.% PyOil and 12.6 wt.% PyGas. SSA increased the PyOil yield to 78.0 wt.% at 1:10 and promoted lighter aromatics; at 1:1, light aromatics increased to 66.8 wt.%, BTEX from 5.8 to 24.58 wt.%, and PAHs decreased to 11.8 wt.%. SSC showed a weaker, non-monotonic effect, with PyOil decreasing to 54.4 wt.% and PyChar increasing to 4.7 wt.% at 1:2. Fe-LSSC produced the strongest changes, increasing PyGas to 28.0 wt.% at 1:1 and H2 to 75.3 vol.% at 1:2. The gasoline-range fraction reached 82.1 wt.% at 1:2, while PAHs decreased to 8.79 wt.% at 1:1. Catalyst reuse altered gas composition, whereas thermal regeneration partially restored catalytic behavior. Overall, SS-derived materials exhibited distinct, loading-dependent catalytic functions, while HCl leaching and Fe impregnation enhanced the conversion of PS pyrolysis vapors toward lighter aromatic and gaseous products.

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Publication Details

Journal
Polymers
Published
2026-09-29
DOI
https://doi.org/10.3390/polym18192372
Primary Topic
Thermochemical Biomass Conversion Processes
Type
article
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article

In-Situ Catalytic Pyrolysis of Polystyrene with Sewage Sludge-Derived Catalysts: Sewage Sludge Ash, Sewage Sludge Char, and Fe-Impregnated Acid-Leached Sewage Sludge Char

N.A. ZABARA, Anara Omarova, Grigoriy A. Mun, Mukhambetkali M. Burkitbayev et al.
Polymers
Thermochemical Biomass Conversion Processes
article

In-Situ Catalytic Pyrolysis of Polystyrene with Sewage Sludge-Derived Catalysts: Sewage Sludge Ash, Sewage Sludge Char, and Fe-Impregnated Acid-Leached Sewage Sludge Char

N.A. ZABARA, Anara Omarova, Grigoriy A. Mun, Mukhambetkali M. Burkitbayev, Sergey Efremov, Aigerim K. Kaiaidarova, Olga P. Ibragimova, Sergey Nechipurenko, Diyar Tokmurzin, Fedor Pogorov, Yelena Vitoshnova
article en

Abstract

Sewage sludge (SS)-derived materials were investigated as low-cost heterogeneous catalytic materials for polystyrene (PS) pyrolysis, focusing on the effects of thermal treatment, HCl leaching, and Fe impregnation. Sewage sludge ash (SSA), sewage sludge char (SSC), and HCl-leached Fe-impregnated sewage sludge char (Fe-LSSC) were evaluated as in-situ catalytic materials. Catalyst-to-PS ratios of 1:1–1:10 were investigated in a horizontal semi-batch tubular reactor operated in an in-situ catalyst–polymer contact mode at 800 °C. Thermal pyrolysis produced 63.9 wt.% PyOil and 12.6 wt.% PyGas. SSA increased the PyOil yield to 78.0 wt.% at 1:10 and promoted lighter aromatics; at 1:1, light aromatics increased to 66.8 wt.%, BTEX from 5.8 to 24.58 wt.%, and PAHs decreased to 11.8 wt.%. SSC showed a weaker, non-monotonic effect, with PyOil decreasing to 54.4 wt.% and PyChar increasing to 4.7 wt.% at 1:2. Fe-LSSC produced the strongest changes, increasing PyGas to 28.0 wt.% at 1:1 and H2 to 75.3 vol.% at 1:2. The gasoline-range fraction reached 82.1 wt.% at 1:2, while PAHs decreased to 8.79 wt.% at 1:1. Catalyst reuse altered gas composition, whereas thermal regeneration partially restored catalytic behavior. Overall, SS-derived materials exhibited distinct, loading-dependent catalytic functions, while HCl leaching and Fe impregnation enhanced the conversion of PS pyrolysis vapors toward lighter aromatic and gaseous products.

PolymersVol. 18(19)
Al-Farabi Kazakh National University (KZ), Ghent University (BE)
Clean water and sanitation
Openalex Percentile: Top 22%
Thermochemical Biomass Conversion Processes
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