Selective Electrocatalytic Degradation of Ether‐Containing Polymers DOI
Jesse H. Hsu, Tyler E. Ball, Sewon Oh

и другие.

Angewandte Chemie, Год журнала: 2023, Номер 136(3)

Опубликована: Ноя. 30, 2023

Abstract Leveraging electrochemistry to degrade robust polymeric materials has the potential impact society's growing issue of plastic waste. Herein, we develop an electrocatalytic oxidative degradation polyethers and poly(vinyl ethers) via electrochemically mediated hydrogen atom transfer (HAT) followed by polymer promoted molecular oxygen. We investigated selectivity efficiency this method, finding our conditions be highly selective for polymers with hydridic, electron‐rich C−H bonds. leveraged reactivity in presence polymethacrylates polyacrylates complete selectivity. Furthermore, method made degradable incorporation ether units into backbone. quantified products, identifying up 36 mol % defined oxidation including acetic acid, formic acetaldehyde, extended a polyether‐based polyurethane green solvent. This work demonstrates facile, electrochemically‐driven route containing functionalities.

Язык: Английский

Electrochemical recycling of polymeric materials DOI Creative Commons
Weizhe Zhang, Lars Killian, Arnaud Thevenon

и другие.

Chemical Science, Год журнала: 2024, Номер 15(23), С. 8606 - 8624

Опубликована: Янв. 1, 2024

Electrochemistry shows promising new avenues in the recycling of polymeric materials. This work reviews electrochemical depolymerization, post-polymerization functionalization, and paired catalysis, highlighting future challenges opportunities.

Язык: Английский

Процитировано

12

Electrochemical Deconstruction of Waste Polyvinylidene Chloride (PVDC) to Value‐Added Products in Batch and Flow DOI Open Access
S. K. Mishra,

Sourav Kar,

Raghavendrakumar Rangappa

и другие.

Chemistry - A European Journal, Год журнала: 2025, Номер unknown

Опубликована: Янв. 22, 2025

Abstract Chlorinated polymers have made enormous contributions to materials science and are commercially produced on a large scale. These chlorinated could be recycled as chlorine sources efficiently produce valuable compounds owing their facile release of HCl. Although the thermal stability PVDC is low compared PVC, this can advantageous in terms easy fast dehydrochlorination. Herein, we report an efficient electrochemical chlorination using poly(vinylidene chloride) (PVDC) source that works undivided cell applies good number examples. This method commodity such waste PVDC‐PVC pharma blister film, PVDC‐PO multilayer food packaging, compression molded sheets Ixan (with heat stabilizer) with similar efficiency. Furthermore, also provides dechlorination up 98 %, leading unsaturated dechlorinated material. Converting into more stable compounds, harmful chlorine‐containing gases during incineration minimized. Additionally, not only restricted batch processes but electroflow process for electrosynthesis has been demonstrated.

Язык: Английский

Процитировано

2

Harnessing Non-Thermal External Stimuli for Polymer Recycling DOI Creative Commons
Glen R. Jones, Richard Whitfield, Hyun Suk Wang

и другие.

Macromolecules, Год журнала: 2025, Номер 58(5), С. 2210 - 2223

Опубликована: Фев. 18, 2025

Polymeric materials have become indispensable due to their versatility and low cost, yet environmental impact presents a significant global challenge. Traditional chemical recycling methods typically rely on heat as stimulus; for instance, pyrolysis is popular methodology which faces limitations high energy consumption, product selectivity, the generation of undesirable byproducts. In response, recent advances in promotion depolymerization degradation through alternative stimuli such light, electrochemistry, mechanical force, shown promising potential more efficient selective polymer breakdown, yielding either starting monomers or valuable small molecules. This perspective explores key examples these emerging strategies, highlighting improve upon current protocols offer pathways under milder conditions, while identifying challenges that future research must address translate chemistry into viable broadly applicable strategies.

Язык: Английский

Процитировано

2

Upcycling of waste polyethylene terephthalate to dimethyl terephthalate over solid acids under mild conditions DOI
Boyong Ye,

Ruru Zhou,

Zixin Zhong

и другие.

Green Chemistry, Год журнала: 2023, Номер 25(18), С. 7243 - 7252

Опубликована: Янв. 1, 2023

The Ti 0.5 Si O 2 solid acid catalyst is extremely active and stable for methanol alcoholysis of polyethylene terephthalate to dimethyl under mild conditions.

Язык: Английский

Процитировано

19

Selective Electrocatalytic Degradation of Ether‐Containing Polymers DOI
Jesse H. Hsu, Tyler E. Ball, Sewon Oh

и другие.

Angewandte Chemie International Edition, Год журнала: 2023, Номер 63(3)

Опубликована: Ноя. 30, 2023

Leveraging electrochemistry to degrade robust polymeric materials has the potential impact society's growing issue of plastic waste. Herein, we develop an electrocatalytic oxidative degradation polyethers and poly(vinyl ethers) via electrochemically mediated hydrogen atom transfer (HAT) followed by polymer promoted molecular oxygen. We investigated selectivity efficiency this method, finding our conditions be highly selective for polymers with hydridic, electron-rich C-H bonds. leveraged reactivity in presence polymethacrylates polyacrylates complete selectivity. Furthermore, method made degradable incorporation ether units into backbone. quantified products, identifying up 36 mol % defined oxidation including acetic acid, formic acetaldehyde, extended a polyether-based polyurethane green solvent. This work demonstrates facile, electrochemically-driven route containing functionalities.

Язык: Английский

Процитировано

15

Challenges and opportunities in catalytic hydrogenolysis of oxygenated plastics waste: polyesters, polycarbonates, and epoxy resins DOI Creative Commons
Harisekhar Mitta, Lingfeng Li, Mohammadhossein Havaei

и другие.

Green Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

This review comprehensively explores various homogeneous and heterogeneous catalytic systems for the hydrogenolysis of oxygenated polymeric wastes (OXPs), presenting an adaptable solution to plastic pollution generating valuable feedstock.

Язык: Английский

Процитировано

5

Anodic Commodity Polymer Recycling: The Merger of Iron‐Electrocatalysis with Scalable Hydrogen Evolution Reaction DOI Creative Commons
Maxime Hourtoule, Sven Trienes, Lutz Ackermann

и другие.

Angewandte Chemie International Edition, Год журнала: 2024, Номер 63(48)

Опубликована: Сен. 10, 2024

Abstract Plastics are omnipresent in our everyday life, and accumulation of post‐consumer plastic waste environment represents a major societal challenge. Hence, methods for recycling high demand future circular economy. Specifically, the degradation polymers towards value‐added small molecules constitutes sustainable strategy carbon Despite recent advances, chemical polymer continues to be largely limited redox agents or low energy efficiency photochemical processes. We herein report powerful iron‐catalyzed molecular weight polystyrenes through electrochemistry efficiently deliver monomeric benzoyl products. The robustness ferraelectrocatalysis was mirrored by various real‐life plastics, also on gram scale. cathodic half reaction represented hydrogen evolution (HER). scalable electro‐polymer could solely fueled solar commercially available panel, indicating an outstanding potential decentralized green

Язык: Английский

Процитировано

3

Production of Plastic-Derived Fuel by Cohydrocracking of Different Polyethylene Terephthalate (PET) with Vacuum Gas Oil (VGO) DOI
David Trueba, Roberto Palos, Iratxe Crespo

и другие.

Energy & Fuels, Год журнала: 2025, Номер unknown

Опубликована: Фев. 6, 2025

To promote the chemical recycling of polyethylene terephthalate (PET), its valorization by hydrocracking was investigated. ease implementation at large-scale this route, PET coprocessed with vacuum gasoil (VGO), which is a benchmark feed industrial unit (10 and 90 wt %, respectively) hydrocracked using PtPd/HY catalyst. Furthermore, suitability PETs different natures origins to produce fuel-assimilable streams assessed. Specifically, one virgin, commercial, mechanically recycled were used, analyzing differences in conversion, yields product fractions (dry gas, liquefied petroleum gases, naphtha, light cycle oil), composition naphtha oil fractions, given their possible interest being used formulation automotive fuels. The reaction runs performed batch reactor under following conditions: 80 bar, 420 °C, 120 min, catalyst/feed mass ratio 10 gcatalyst gfeed–1. modified degraded plastics more easily converted into liquid hydrocarbons within LCO contents isoparaffins between 45 50 %. From products, pathways PET-derived molecules evaluated.

Язык: Английский

Процитировано

0

Advancements in the Electrochemical Upcycling of Waste Plastics into High-Value Products DOI Creative Commons
Jin Woo Kim,

Shokouh Masoumilari,

Yeojin Park

и другие.

Crystals, Год журнала: 2025, Номер 15(4), С. 293 - 293

Опубликована: Март 24, 2025

The growing plastic waste crisis calls for innovative and sustainable solutions that go beyond traditional recycling methods. Electrochemical upcycling has emerged as a promising approach converting plastics into valuable chemicals, fuels, functional materials. Recent advancements in electrochemical strategies valorization focus on key catalysts, reaction mechanisms, process efficiencies. studies place special emphasis new techniques aimed at improving selectivity, energy efficiency, scalability. Additionally, integrating renewable sources optimizing electrode materials have significantly enhanced sustainability. This review specifically focuses recent research, which addresses the challenges of waste.

Язык: Английский

Процитировано

0

Electrolytic upcycling of PET waste plastics for energy-efficient hydrogen evolution DOI
Guohao Xu, Zhaopeng Sun, Kai He

и другие.

Green Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

We achieved the conversion of waste PET into TPA and hydrogen energy under mildly acidic conditions (100 °C; acid concentration <2.5 mol L −1 ).

Язык: Английский

Процитировано

0