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来自聚乙烯升级循环衍生碳氢化合物反应分离的阴离子表面活性剂

Anionic Surfactants from Reactive Separation of Hydrocarbons Derived from Polyethylene Upcycling.

作者信息

Lee Yu-Hsuan, Heuston Alexandra, Jin Enze, Sun Jiakai, Liang Xichen, Zhu Yangying, Helgeson Matthew E, Masanet Eric, Scott Susannah L, Abu-Omar Mahdi M

机构信息

Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106-9510, United States.

Bren School of Environmental Science & Management, University of California, Santa Barbara, California 93106-5131, United States.

出版信息

Langmuir. 2025 Feb 18;41(6):3995-4004. doi: 10.1021/acs.langmuir.4c04277. Epub 2025 Feb 4.

DOI:10.1021/acs.langmuir.4c04277
PMID:39901800
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11841028/
Abstract

Chemical upcycling of polyethylene (PE) to long-chain alkylaromatics through tandem hydrocracking/aromatization has potential to provide value-added chemicals. However, the liquid product is a complex mixture of alkanes, alkylbenzenes, and polyaromatics, limiting its direct usability. The most valuable component of the product mixture is the alkylbenzenes because of their potential as precursors to anionic surfactants. In this study, a one-pot reactive separation is described. Sulfonating the product mixture from PE upcycling with silica sulfuric acid followed by neutralization with sodium hydroxide yields sodium alkylbenzenesulfonates (up to 93 mol % selectivity), along with a separate phase of lubricant-range hydrocarbons as a coproduct. Compared to petroleum-based sodium dodecylbenzenesulfonates, the reported PE-derived surfactant molecules show competitive physicochemical properties, including surface tension and interfacial tension. According to life cycle assessment, the described reaction strategy demonstrates 20% lower greenhouse gas emissions, when considering uses for the coproducts of PE upcycling, compared to conventional linear alkylbenzenesulfonates (LAS) manufacturing directly from petrochemical feedstocks.

摘要

通过串联加氢裂化/芳构化将聚乙烯(PE)化学升级循环为长链烷基芳烃有潜力提供增值化学品。然而,液体产物是烷烃、烷基苯和多芳烃的复杂混合物,限制了其直接可用性。产物混合物中最有价值的成分是烷基苯,因为它们有作为阴离子表面活性剂前体的潜力。在本研究中,描述了一种一锅法反应分离过程。用硅胶硫酸对PE升级循环的产物混合物进行磺化,然后用氢氧化钠中和,得到烷基苯磺酸钠(选择性高达93 mol%),同时还有作为副产物的润滑剂级烃的分离相。与石油基十二烷基苯磺酸钠相比,所报道的源自PE的表面活性剂分子表现出具有竞争力的物理化学性质,包括表面张力和界面张力。根据生命周期评估,与直接由石化原料制造的传统直链烷基苯磺酸盐(LAS)相比,当考虑PE升级循环副产物的用途时,所描述的反应策略显示温室气体排放量降低了20%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/3bc5687f4bde/la4c04277_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/7126623d5859/la4c04277_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/f7b7fa7a1857/la4c04277_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/f138e8c9fdf2/la4c04277_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/080c33b72fe1/la4c04277_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/3bc5687f4bde/la4c04277_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/7126623d5859/la4c04277_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/f7b7fa7a1857/la4c04277_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/f138e8c9fdf2/la4c04277_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/080c33b72fe1/la4c04277_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12eb/11841028/3bc5687f4bde/la4c04277_0005.jpg

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本文引用的文献

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通过多相催化对具有碳-碳主链的废塑料进行升级再造。
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