Achieving Exceptional Thermal and Hydrolytic Resistance in Chemically Circular Polyesters via In‐Chain 1,3‐Cyclobutane Rings DOI
Chaoqun Weng,

Zhiqiang Ding,

Weijie Qiu

et al.

Angewandte Chemie, Journal Year: 2024, Volume and Issue: 136(24)

Published: April 8, 2024

Abstract Polyesters, a highly promising class of circular polymers for achieving closed‐loop sustainable plastic economy, inherently exhibit material stability defects, especially in thermal and hydrolytic instability. Here, we introduce polyesters, P(4 R ‐BL) (R=Ph, Bu), featuring conformationally rigid 1,3 ‐ cyclobutane rings the backbone. These polyesters not only superior thermostability ( T d,5% =376–380 °C) but also demonstrate exceptional resistance with good integrity even after 1 year basic acidic aqueous solutions, distinguishing themselves from typical counterparts. Tailoring flexibility side group enables controlled mechanical performance Ph Bu to rival durable syndiotactic polystyrene (SPS) low‐density polyethylene (LDPE), respectively. Significantly, despite their high stability, both can be effectively depolymerized into pristine monomers, establishing life cycle.

Language: Английский

Achieving Exceptional Thermal and Hydrolytic Resistance in Chemically Circular Polyesters via In‐Chain 1,3‐Cyclobutane Rings DOI
Chaoqun Weng,

Zhiqiang Ding,

Weijie Qiu

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(24)

Published: April 8, 2024

Abstract Polyesters, a highly promising class of circular polymers for achieving closed‐loop sustainable plastic economy, inherently exhibit material stability defects, especially in thermal and hydrolytic instability. Here, we introduce polyesters, P(4 R ‐BL) (R=Ph, Bu), featuring conformationally rigid 1,3 ‐ cyclobutane rings the backbone. These polyesters not only superior thermostability ( T d,5% =376–380 °C) but also demonstrate exceptional resistance with good integrity even after 1 year basic acidic aqueous solutions, distinguishing themselves from typical counterparts. Tailoring flexibility side group enables controlled mechanical performance Ph Bu to rival durable syndiotactic polystyrene (SPS) low‐density polyethylene (LDPE), respectively. Significantly, despite their high stability, both can be effectively depolymerized into pristine monomers, establishing life cycle.

Language: Английский

Citations

7

cis-Fused cyclohexane promoted the chemical recycling of polycarbonate to monomer DOI

Si‐Yi Shan,

Wei Zhang, Qing Cao

et al.

Polymer Chemistry, Journal Year: 2024, Volume and Issue: 15(11), P. 1070 - 1076

Published: Jan. 1, 2024

A seven-membered cyclic carbonate bearing a cis -fused cyclohexane structure enabled the chemical recycling of polycarbonate to high-ring-strain monomer.

Language: Английский

Citations

6

Chemical recycling to monomer: thermodynamic and kinetic control of the ring-closing depolymerization of aliphatic polyesters and polycarbonates DOI Creative Commons

Linnea Cederholm,

Peter Olsén, Minna Hakkarainen

et al.

Polymer Chemistry, Journal Year: 2023, Volume and Issue: 14(28), P. 3270 - 3276

Published: Jan. 1, 2023

The study investigates the potential in solvent triggered chemical recycling and how power of effect is influenced by monomer structure. Catalyst selectivity utilized to demonstrate mixed polymer waste.

Language: Английский

Citations

14

Facile, high-efficiency, and low-cost depolymerization of PA6 to ϵ-caprolactam enables closed-loop chemical recycling DOI
Xiaohe Chen, Gang Wu, Si‐Chong Chen

et al.

Polymer, Journal Year: 2023, Volume and Issue: 283, P. 126201 - 126201

Published: July 18, 2023

Language: Английский

Citations

14

Tetrabutylammonium Halides as Selectively Bifunctional Catalysts Enabling the Syntheses of Recyclable High Molecular Weight Salicylic Acid‐Based Copolyesters DOI Open Access

Fangping Ren,

Ji Xian,

Zhaowei Jia

et al.

Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(44)

Published: Sept. 15, 2023

To synthesize high molecular weight poly(phenolic ester) via a living ring-opening polymerization (ROP) of cyclic phenolic ester monomers remains critical challenge due to serious transesterification and back-biting reactions. Both bonds in monomer polymer chains are highly active, it is difficult so far distinguish them. In this work, an unprecedented selectively bifunctional catalytic system tetra-n-butylammonium chloride (TBACl) was discovered mediate the syntheses salicylic acid-based copolyesters ROP salicylate esters (for poly(salicylic methyl glycolide) (PSMG), Mn =361.8 kg/mol, Ð<1.30). Compared previous catalysis systems, side reactions were suppressed remarkably because bond can be cleaved over that during progress. Mechanistic studies reveal halide anion alkyl-quaternaryammonium cation work synergistically, where moiety interacts with carbonyl group substrates non-classical hydrogen bonding. Moreover, these recycled dimeric under solution condition, original monomeric without catalyst sublimation condition.

Language: Английский

Citations

11

Polyheptenamer: A chemically recyclable polyolefin enabled by the low strain of seven‐membered cycloheptene DOI
Tarek Ibrahim,

J. G. Martindale,

Angelo Ritacco

et al.

Journal of Polymer Science, Journal Year: 2024, Volume and Issue: 62(21), P. 4921 - 4927

Published: April 25, 2024

Abstract Low‐strain cyclic olefin monomers, including five‐membered, six‐membered, eight‐membered, and macrocyclic rings, have been recently exploited for the synthesis of depolymerizable polyolefins via ring‐opening metathesis polymerization (ROMP). Such can undergo ring‐closing depolymerization (RCMD) to regenerate their original monomers. Nevertheless, behavior prepared by ROMP seven‐membered olefins, an important class low‐strain still remains unexplored. In this study, we demonstrate chemical recycling polyheptenamers cycloheptene under standard RCMD conditions. Highly efficient polyheptenamer was enabled Grubbs' second‐generation catalyst in toluene. It observed that monomer yields increased when temperature starting polymer concentration reduced. A near‐quantitative regeneration (>96%) achieved within 1 h dilute conditions (20 mM olefins) at 60°C. Moreover, exhibited a decomposition above 430°C, highlighting its potential as new thermally stable chemically recyclable materials.

Language: Английский

Citations

4

Amino acids as bio-organocatalysts in ring-opening copolymerization for eco-friendly synthesis of biobased oligomers from vegetable oils DOI

Francisca Werlinger,

Monserrat Beroíza-Duhart,

Oscar A. Douglas‐Gallardo

et al.

Organic & Biomolecular Chemistry, Journal Year: 2024, Volume and Issue: 22(20), P. 4135 - 4144

Published: Jan. 1, 2024

This is the first contribution reported to date in literature which natural precursors such as amino acids (AAs) have been effectively employed bio-organocatalysts for preparation of biobased polyesters.

Language: Английский

Citations

4

Chemical Closed-loop Recycling of Polymers Realized by Monomer Design DOI Creative Commons
Wuchao Zhao, Jianghua He, Yuetao Zhang

et al.

Fundamental Research, Journal Year: 2024, Volume and Issue: unknown

Published: June 1, 2024

The development of modern society is closely related to polymer materials. However, the improper disposal wastes not only squanders resources but also intensifies environmental issues, despite that energy recovery, physical recycling and chemical pathways have been developed tackle recycle reuse polymers. Among them, considered as most pivotal solution, it can depolymerize back monomers, which then repolymerize into Recently, remarkable progress has made in chemically recyclable polymers through monomer design shift "polymerization-depolymerization" equilibrium realize selective depolymerization achieve closed-loop. This article reviews closed-loop such polyesters, polycarbonates, sulfur-containing polymers, vinyl monomer-based well other types Moreover, challenges prospects this field are discussed.

Language: Английский

Citations

4

Solvent-Free One-Pot Recycling of Polylactide to Usable Polymers and Their Closed-Loop Recyclability DOI

Zixuan Luo,

Guoqiang Tian, Si‐Chong Chen

et al.

Macromolecules, Journal Year: 2024, Volume and Issue: 57(14), P. 6828 - 6837

Published: July 10, 2024

Language: Английский

Citations

4

Functional Polyesters: Tailoring Structure and Biomedical Functions DOI Creative Commons
Zhitao Hu, Ming Li, Yongming Chen

et al.

Polymer science & technology., Journal Year: 2025, Volume and Issue: unknown

Published: March 21, 2025

Language: Английский

Citations

0