We can't find the internet
Attempting to reconnect
Something went wrong!
Hang in there while we get back on track
Fully Recyclable Polycarbonates from Simple, Bio-Derived Building Blocks
AI summary Read the abstract
Bio-based polycarbonates from glycerol with two end-of-life options: chemical recycling or environmental decomposition.
Plastic buildup and accumulation in the environment are an increasingly large problem facing civilization. Petroleum-based plastics can exist for hundreds to thousands of years in the environment, destroying habitats and polluting water. Environmentally conscious replacements for plastics are urgently needed. In this publication, we present a biobased alternative to petroleum-based polycarbonates. Using a diol monomer derived from glycerol and glycerol products, we have synthesized aliphatic polycarbonates with comparable physical properties to petroleum-based incumbents. The polymer can be quantitatively depolymerized using warm methanol to recover the monomer which can be repolymerized multiple times, or alternatively, the monomer, which is inherently nontoxic, can slowly break apart to the original components. This provides two end-of-life options for this material recycle or decomposition under environmental conditions to benign building blocks, thus providing a potential pathway to avoid environmental and bioaccumulation of plastics. We also demonstrate the ability to selectively recover the monomer from a simulated mixed-plastic waste environment; the monomer recovered this way functions identically to the virgin monomer after purification. This work represents an important step in the progress toward environmentally conscious polymer design with multiple end-of-life options.
More Papers Like This
Catalysis as an Enabling Science for Sustainable Polymers
AI summary Read the abstract
Researchers reviewed how catalysis can enable the development of sustainable, bio-based polymers to replace petroleum-derived plastics, analyzing the full system from feedstock to end-of-life and identifying catalytic strategies that improve degradability, recyclability, and carbon footprint.
Bicyclic Guanidine Promoted Mechanistically Divergent Depolymerization and Recycling of a Biobased Polycarbonate
AI summary Read the abstract
Researchers demonstrated that the organic catalyst TBD can break down biobased poly(limonene carbonate) through two temperature-controlled pathways — end-group activation or main-chain scission — selectively recovering a cyclic carbonate monomer that can then be re-polymerized using the same catalyst, enabling a circular recycling route.
High-throughput computational analysis of kinetic barriers to ring-closing depolymerization for aliphatic polycarbonates
AI summary Read the abstract
Researchers used high-throughput computational modeling to calculate energy barriers for ring-closing depolymerization of aliphatic polycarbonates, finding that results matched prior experimental trends and confirming that functional group variation significantly influences whether a polymer can be cleanly reverted to reusable monomers for chemical recycling.
Redesigning Carbon–Carbon Backbone Polymers for Biodegradability–Compostability at the End-of-Life Stage
AI summary Read the abstract
This review discusses strategies for redesigning carbon-carbon backbone polymers, which comprise 77% of global plastics, to be biodegradable and compostable at end-of-life, addressing the persistent microplastic pollution problem caused by conventional non-biodegradable plastics.
Depolymerization within a Circular Plastics System
AI summary Read the abstract
This review examines chemical depolymerization as a route to producing virgin-quality recycled plastics from complex waste streams that mechanical recycling cannot handle, covering five commercial polymers including PET, polycarbonates, and polyurethanes. The authors argue that depolymerization must be understood within the broader system of recycling technologies and economic constraints to advance a truly circular plastics economy.
Research digests by email
When a large batch of papers lands in the Atlas, we read through it and send a short write-up of what stood out.