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通过协同催化剂将废弃聚对苯二甲酸乙二酯转化为高价值单体

Converting Waste Polyethylene Terephthalate to High Value Monomers by Synergistic Catalysts.

作者信息

Wu Junyan, Yang Fan, Shi Diandian, Miao Zhen, Wang Jue, Wang Dianyu, Zhang Yadong

机构信息

School of Chemical Engineering, Zhengzhou University, Zhengzhou, CN-450001, China.

Jiyuan Research Institute, Zhengzhou University, Jiyuan, CN-459000, China.

出版信息

ChemSusChem. 2025 Feb 16;18(4):e202401922. doi: 10.1002/cssc.202401922. Epub 2024 Nov 7.

Abstract

Waste plastics accumulation, such as commonly used polyethylene terephthalate (PET), has caused serious environmental pollution and resource squander. Glycolysis is a reliable closed-loop PET recycling method, which limited by the high cost and complex catalysts preparation processes. Here we report a simple synergistic catalytic strategy by premixing zinc acetate and cheap alkalis in ethylene glycol, which could achieve complete glycolysis at 180 °C within 2 hours, and a bis(hydroxyethyl) terephthalate (BHET) yield of 86.4 %. This may be attributed to the free hydroxide ions not only enhancing the nucleophilicity of oxygen in ethylene glycol and making it easy to attack carbonyl groups, but also accelerating the swelling and dissolution of PET. Meanwhile, the in-situ generated Zn-glycolate and zinc oxide nanoparticles (ZnO NPs) activated the oxygen in the carbonyl group, making the carbon cations more electropositive. Further recycling experiments and techno-economic analysis indicated that our synergistic strategy significantly reduced industrial costs and expected to achieve large-scale industrial applications.

摘要

废旧塑料的堆积,如常用的聚对苯二甲酸乙二酯(PET),已造成严重的环境污染和资源浪费。乙二醇解是一种可靠的PET闭环回收方法,但受到高成本和复杂催化剂制备过程的限制。在此,我们报道了一种简单的协同催化策略,即将醋酸锌和廉价碱在乙二醇中预混合,该策略可在180°C下2小时内实现完全乙二醇解,对苯二甲酸双(2-羟乙基)酯(BHET)产率达86.4%。这可能归因于游离的氢氧根离子不仅增强了乙二醇中氧的亲核性,使其易于进攻羰基,还加速了PET的溶胀和溶解。同时,原位生成的乙醇酸锌和氧化锌纳米颗粒(ZnO NPs)激活了羰基中的氧,使碳阳离子更正电。进一步的回收实验和技术经济分析表明,我们的协同策略显著降低了工业成本,并有望实现大规模工业应用。

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