Phase-Selective Organogelators with pH-Triggered Recovery for Efficient Oil Spill Treatment

Oil spill pollution poses a severe environmental threat, necessitating the development of efficient and sustainable remediation strategies. In this study, we designed and synthesized a series of pH-responsive phase-selective organogelators (pRPSOGs) based on d-gluconic acetal derivatives with long-chain amine groups to selectively solidify oil in oil/water mixtures, facilitating its rapid removal and recovery. The gelation behavior, phase-selective capability, and pH-switchable properties of the synthesized pRPSOGs were systematically investigated by using inversion tests, rheological analysis, Fourier transform infrared spectroscopy, X-ray diffraction, and small-angle X-ray scattering. Molecular simulations were further conducted to elucidate the self-assembly mechanism of the gelators. The optimized gelator, A<sub>12</sub>, exhibited excellent thermal stability and mechanical strength, ensuring structural integrity during oil spill recovery. Importantly, the pH-responsive property of A<sub>12</sub> allowed for reversible solubility modulation, enabling efficient separation and recovery of both the gelator and oil phase without the need for energy-intensive distillation. This innovative strategy provided a reusable, energy-efficient, and environmentally friendly approach for oil spill treatment, offering promising applications for large-scale environmental remediation.

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Publication Details

Journal
Langmuir
Published
2025-05-19
DOI
https://doi.org/10.1021/acs.langmuir.5c01318
Citations
3
Primary Topic
Supramolecular Self-Assembly in Materials
Type
article
Field-Weighted Citation Impact
1.79

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article

Phase-Selective Organogelators with pH-Triggered Recovery for Efficient Oil Spill Treatment

Xuezhong Zhang, Zongjin Li, Guilong Yan, Lihua Zhou et al.
3 citations
Langmuir
Supramolecular Self-Assembly in Materials
1.79
article

Phase-Selective Organogelators with pH-Triggered Recovery for Efficient Oil Spill Treatment

Xuezhong Zhang, Zongjin Li, Guilong Yan, Lihua Zhou, Jingyu Chen, Jingjuan Lai, Dong Xiang, Yuanpeng Wu, Xungai Wang, Zhenyu Li, Li Wang, Dong Li, Hui Li, Han Li, Chunxia Zhao, Bo Yu, Yi Zheng, Yi Zeng, R.S. Yin
article en
3 citations

Abstract

Oil spill pollution poses a severe environmental threat, necessitating the development of efficient and sustainable remediation strategies. In this study, we designed and synthesized a series of pH-responsive phase-selective organogelators (pRPSOGs) based on d-gluconic acetal derivatives with long-chain amine groups to selectively solidify oil in oil/water mixtures, facilitating its rapid removal and recovery. The gelation behavior, phase-selective capability, and pH-switchable properties of the synthesized pRPSOGs were systematically investigated by using inversion tests, rheological analysis, Fourier transform infrared spectroscopy, X-ray diffraction, and small-angle X-ray scattering. Molecular simulations were further conducted to elucidate the self-assembly mechanism of the gelators. The optimized gelator, A<sub>12</sub>, exhibited excellent thermal stability and mechanical strength, ensuring structural integrity during oil spill recovery. Importantly, the pH-responsive property of A<sub>12</sub> allowed for reversible solubility modulation, enabling efficient separation and recovery of both the gelator and oil phase without the need for energy-intensive distillation. This innovative strategy provided a reusable, energy-efficient, and environmentally friendly approach for oil spill treatment, offering promising applications for large-scale environmental remediation.

LangmuirVol. 41(21)
Hong Kong Polytechnic University (HK), Southwest Petroleum University (CN), State Key Laboratory of Oil and Gas Reservoir Geology and Exploitation (CN)
National Natural Science Foundation of China, Southwest Petroleum University, Department of Science and Technology of Sichuan Province, State Key Laboratory of Oil and Gas Reservoir Geology and Exploitation
Openalex Percentile: Top 16%
Supramolecular Self-Assembly in Materials
1.79
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