Rapidly Reprocessable Cross-Linked Polyhydroxyurethanes Based on Disulfide Exchange DOI
David J. Fortman, Rachel L. Snyder, Daylan T. Sheppard

и другие.

ACS Macro Letters, Год журнала: 2018, Номер 7(10), С. 1226 - 1231

Опубликована: Сен. 20, 2018

Polymer networks that are cross-linked by dynamic covalent bonds often sacrifice the robust mechanical properties of traditional thermosets in exchange for rapid and efficient reprocessability. Polyurethanes attractive materials reprocessable polymers because their excellent properties, widespread use, ease synthesis, but syntheses typically rely on harmful isocyanate precursors. Polyhydroxyurethanes (PHUs), derived from amines cyclic carbonates, promising alternatives to polyurethanes. PHU via transcarbamoylation reactions even absence external catalysts, this process occurs over hours at temperatures above 150 °C. We have dramatically shortened reprocessing times incorporating disulfide bonds. Using cystamine as a comonomer gives with similar thermal stability other rigid PHUs. Despite these show stress relaxation characteristic low 30 s This property enables quantitative recovery cross-link density measured DMTA after only min elevated-temperature compression molding. Disulfide incorporation is approach obtain reprocessable, resins not isocyanates.

Язык: Английский

Self-healing polymers DOI
Siyang Wang, Marek W. Urban

Nature Reviews Materials, Год журнала: 2020, Номер 5(8), С. 562 - 583

Опубликована: Июнь 5, 2020

Язык: Английский

Процитировано

1021

Adaptable Crosslinks in Polymeric Materials: Resolving the Intersection of Thermoplastics and Thermosets DOI
Georg M. Scheutz, Jacob J. Lessard, Michael B. Sims

и другие.

Journal of the American Chemical Society, Год журнала: 2019, Номер 141(41), С. 16181 - 16196

Опубликована: Сен. 16, 2019

The classical division of polymeric materials into thermoplastics and thermosets based on covalent network structure often implies that these categories are distinct irreconcilable. Yet, the past two decades have seen extensive development bridge this gap through incorporation dynamic crosslinks, enabling them to behave as both robust networks moldable plastics. Although their potential utility is significant, growth adaptable (CANs) has obscured line between "thermoplastic" "thermoset" erected a conceptual barrier growing number new researchers entering discipline. This Perspective aims outline fundamental theory CANs provide critical assessment current status. We emphasize throughout unique properties emerge from chemistry, particularly highlight role crosslink exchange mechanism (i.e., dissociative or associative exchange) plays in resultant material under processing conditions. Predominant focus will be thermally induced behavior, majority presently employed chemistries rely thermal stimulus, it simple apply bulk materials. Lastly, identify issues address possible solutions for better understanding within field.

Язык: Английский

Процитировано

705

Closed-loop recycling of plastics enabled by dynamic covalent diketoenamine bonds DOI
Peter R. Christensen, Angelique M. Scheuermann,

Kathryn E. Loeffler

и другие.

Nature Chemistry, Год журнала: 2019, Номер 11(5), С. 442 - 448

Опубликована: Апрель 22, 2019

Язык: Английский

Процитировано

558

Vitrimers: Permanently crosslinked polymers with dynamic network topology DOI Creative Commons
Nathan J. Van Zee, Renaud Nicolaÿ

Progress in Polymer Science, Год журнала: 2020, Номер 104, С. 101233 - 101233

Опубликована: Март 15, 2020

Язык: Английский

Процитировано

544

Dynamic covalent chemistry in polymer networks: a mechanistic perspective DOI Creative Commons
Johan M. Winne, Ludwik Leibler, Filip Du Prez

и другие.

Polymer Chemistry, Год журнала: 2019, Номер 10(45), С. 6091 - 6108

Опубликована: Янв. 1, 2019

A selection of dynamic chemistries is highlighted, with a focus on the reaction mechanisms molecular network rearrangements, and how mechanistic profiles can be related to mechanical physicochemical properties polymer materials.

Язык: Английский

Процитировано

534

Approaches to Sustainable and Continually Recyclable Cross-Linked Polymers DOI Creative Commons
David J. Fortman,

Jacob P. Brutman,

Guilhem X. De Hoe

и другие.

ACS Sustainable Chemistry & Engineering, Год журнала: 2018, Номер 6(9), С. 11145 - 11159

Опубликована: Авг. 26, 2018

Cross-linked polymers are ubiquitous in daily life, finding applications as tires, insulation, adhesives, automotive parts, and countless other products. The covalent cross-links these materials render them mechanically robust, chemically resistant, thermally stable, but they also prevent recycling of into similar-value goods. Furthermore, cross-linked typically produced from petroleum-based feedstocks, their hydrocarbon backbones nondegradable, making unsustainable the long term. In recent years, much effort has focused on development strategies for polymeric materials. following Perspective, we discuss many approaches, highlight efforts to sustainably produce recyclable polymers. We present our thoughts future challenges that must be overcome enable widespread, viable, more sustainable practical implementation materials, including sourcing long-term environmental stability inherently dynamic polymers, moving toward industrially viable synthesis reprocessing methods.

Язык: Английский

Процитировано

445

Toward Stimuli‐Responsive Dynamic Thermosets through Continuous Development and Improvements in Covalent Adaptable Networks (CANs) DOI
Maciej Podgórski,

Benjamin D. Fairbanks,

Bruce E. Kirkpatrick

и другие.

Advanced Materials, Год журнала: 2020, Номер 32(20)

Опубликована: Фев. 14, 2020

Abstract Covalent adaptable networks (CANs), unlike typical thermosets or other covalently crosslinked networks, possess a unique, often dormant ability to activate one more forms of stimuli‐responsive, dynamic covalent chemistries as means transition their behavior from that viscoelastic solid material with fluid‐like plastic flow. Upon application stimulus, such light irradiation, temperature, even distinct chemical signal, the CAN responds by transforming state temporal plasticity through activation either reversible addition bond exchange, which allows essentially re‐equilibrate an altered set conditions are those in original network is formed, simultaneously enabling new and shape, function, characteristics. As such, CANs span divide between thermoplastics, thus offering unprecedented possibilities for innovation polymer materials science. Without attempting comprehensively review literature, recent developments discussed here emphasis on most effective render these be stimuli responsive, features make broadly applicable.

Язык: Английский

Процитировано

417

Vitrimers: Associative dynamic covalent adaptive networks in thermoset polymers DOI
Balaji Krishnakumar, R. V. Siva Prasanna Sanka, Wolfgang H. Binder

и другие.

Chemical Engineering Journal, Год журнала: 2019, Номер 385, С. 123820 - 123820

Опубликована: Дек. 16, 2019

Язык: Английский

Процитировано

396

Recyclable, Strong, and Highly Malleable Thermosets Based on Boroxine Networks DOI

William A. Ogden,

Zhibin Guan

Journal of the American Chemical Society, Год журнала: 2018, Номер 140(20), С. 6217 - 6220

Опубликована: Май 7, 2018

Traditional thermoset materials have favorable material properties but are unable to reprocess and difficult recycle. Small molecule boroxines been shown undergo a reversible exchange reaction. Herein we employ boroxine as dynamic cross-links construct novel type of that is strong, highly malleable, recyclable. The synthesis mechanical networks described. Upon heating in water the can be recycled back its monomer. With multitude tunable variables, anticipate this system platform for development range new materials.

Язык: Английский

Процитировано

333

A fully bio-based epoxy vitrimer: Self-healing, triple-shape memory and reprocessing triggered by dynamic covalent bond exchange DOI Creative Commons
Xinxin Yang,

Lizhen Guo,

Xu Xu

и другие.

Materials & Design, Год журнала: 2019, Номер 186, С. 108248 - 108248

Опубликована: Ноя. 12, 2019

Vitrimers are a new type of polymers with promising applications in innovative materials. Epoxidized soybean oil (ESO) is an ideal candidate for vitrimer preparation owing to its abundant epoxy groups. However, preparing plant oil-based vitrimers high glass transition temperatures (Tg) and strength remains challenging. A novel fully bio-based Tg above room temperature was synthesized from ESO rosin derivative-fumaropimaric acid (FPA) exhibited excellent self-healing, shape memory, reprocessing due the presence dynamic covalent bond exchange. The ESO-FPA 65 °C tensile 16 MPa, which resulted rigid structure tricarboxylic groups FPA. effect transesterification reactions on network confirmed through stress relaxation. Our work expands commercial materials provides approach prepare desirable properties.

Язык: Английский

Процитировано

322