Full control over the ceiling temperature (T) enables a selective transition between the monomeric and polymeric state. This is exemplified by the conversion of the monomer 2-allyloxymethyl-2-ethyl-trimethylene carbonate (AOMEC) to poly(AOMEC) and back to AOMEC within 10 h by controlling the reaction from conditions that favor ring-opening polymerization (T > T) (where T is the reaction temperature) to conditions that favor ring-closing depolymerization (T < T). The ring-closing depolymerization (RCDP) mirrors the polymerization behavior with a clear relation between the monomer concentration and the molecular weight of the polymer, indicating that RCDP occurs at the chain end. The T of the polymerization system is highly dependent on the nature of the solvent, for example, in toluene, the T of AOMEC is 234 °C and in acetonitrile T = 142 °C at the same initial monomer concentration of 2 M. The control over the monomer to polymer equilibrium sets new standards for the selective degradation of polymers, the controlled release of active components, monomer synthesis and material recycling. In particular, the knowledge of the monomer to polymer equilibrium of polymers in solution under selected environmental conditions is of paramount importance for in vivo applications, where the polymer chain is subjected to both high dilution and a high polarity medium in the presence of catalysts, that is, very different conditions from which the polymer was formed.
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http://dx.doi.org/10.1021/acs.biomac.6b01375 | DOI Listing |
ACS Macro Lett
December 2024
Department Institute of Materials, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne 1015, Switzerland.
Recovering monomers from the depolymerization of thermosets presents a significant challenge, which becomes even more daunting if one sets the goal of doing it directly, i.e., without complex chemical separation steps.
View Article and Find Full Text PDFRSC Adv
November 2024
Zeon Corporation R&D Center 1-2-1 Yako, Kawasaki-ward Kawasaki-city Kanagawa-pref. 210-9507 Japan +81-44-276-3957 +81-80-1006-7136.
Herein, we report a study on the preparation, properties, and depolymerization of pristine and vulcanized poly(cyclopentene) (poly(CP)), poly(norbornene--cyclopentene) (poly(NB--CP)) and poly(-dicyclopentadiene--cyclopentene) (poly (DCP--CP)). First, poly(CP), poly(NB--CP) and poly(DCP--CP) were prepared with high molecular weight control ( = 200 000-500 000) using dichloro(3-phenyl-1-inden-1-ylidene)bis(tricyclohexylphosphine)ruthenium(ii). Next, carbon black, zinc oxide and other additives were blended into the pristine polymers using a mixer and twin roll rubber mills at 50 °C, followed by vulcanization in metal molds at 160 °C for 10 min, resulting in molded black rubber specimens.
View Article and Find Full Text PDFACS Macro Lett
November 2024
Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
We report the mechanical performance and chemical recycling advantages of implementing alkyl-substituted poly(ε-caprolactones) (PCLs) as soft segments in thermoplastic poly(urethane-urea) (TPUU) materials. Poly(4-methylcaprolactone) (P4MCL) and poly(4-propylcaprolactone) (P4PrCL) were prepared, reacted with isophorone diisocyanate, and chain-extended with water to form TPUUs. The resulting materials' tensile properties were similar or superior to a commercially available polyester thermoplastic poly(urethane) and had superior elastic recovery properties compared to a PCL analogue due to the noncrystalline nature of P4MCL and P4PrCL.
View Article and Find Full Text PDFJ Am Chem Soc
September 2024
Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523-1872, United States.
Developing a mechanistic understanding of catalyzed melt-phase depolymerization processes is of utmost importance to the rapidly expanding field of circular polymers with a closed chemical loop. Herein, we present a methodology to probe the mechanism of metal-catalyzed melt-phase depolymerization of polyesters utilizing an approach centered on studies of kinetics by thermogravimetric analysis and model reactions. Kinetic parameters associated with the prototypical Lewis-acid-catalyzed depolymerization of representative polyesters, including poly(δ-valerolactone) (PVL), poly(lactic acid), and poly(γ-butyrolactone), are elucidated.
View Article and Find Full Text PDFACS Polym Au
June 2024
Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida 32303, United States.
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