Waste plastic and carbon dioxide are two major global waste carbon sources. A new study in Engineering introduces a simple, atmospheric-pressure catalytic method that turns polyethylene and CO₂ into high-value separable aromatics. Using a specially designed oxide–zeolite catalyst, the process delivers high selectivity and stable performance, turning two pollutants into useful petrochemical materials efficiently.

Discarded polyolefin plastics pose severe environmental risks, yet efficient recycling remains challenging. A new study in Engineering presents a simple entropy‑engineering method using silane agents to adjust catalyst surface polarity. This approach stabilizes polymer adsorption, boosts hydrogenolysis activity, and turns waste plastics into high‑value liquid fuels. It works for various catalysts and real‑world plastic wastes, showing strong potential for scalable, sustainable plastic upcycling.

Discarded PET plastic brings serious environmental pressure. A latest study in Engineering offers a green and controllable recycling solution. Without extra catalysts, it uses 1,4-cyclohexanedimethanol (CHDM) to gently break down PET into adjustable oligomers guided by kinetic models. These intermediates can be directly reused to make high-performance elastomers and glycol-modified PET, showing good industrial scalability and promising a more sustainable way for plastic circular economy.

Discarded PET plastic bottles and waste can now be turned into two high-value chemicals without extra hydrogen. A study in Engineering introduces a mild, two-step method using a common Ru/C catalyst to convert PET and methanol into lactic acid and 1,4-cyclohexanedicarboxylic acid. This green approach makes full use of plastic waste’s carbon and hydrogen, offering a sustainable way for plastic upcycling.

Polyurethane (PU) is one of the most widely used plastics, yet recycling it has long been difficult. A new study in Engineering shares recent progress in chemical recycling methods, including hydrogenation, acidolysis, and chem-solvolysis, that can break down PU into reusable raw materials. It explains how these approaches support a circular economy, while pointing out key challenges for moving lab research into real industrial applications.

Plastic pollution poses a growing global threat, while traditional recycling methods suffer from high costs and low efficiency. A new article in Engineering explores promising biocatalytic solutions for plastic depolymerization, including AI-designed enzymes and multi-enzyme systems. These mild, eco-friendly approaches show potential to break down plastics like PET and PUR more effectively, supporting sustainable recycling and the shift toward a circular plastic economy.

A new review synthesizes a decade of research into one of the most promising materials for water purification, biochar–hydrogel composites, and concludes that their effectiveness is governed by a single, critical factor: the chemistry of their surfaces. The work, led by corresponding author Dr. Dong Hee Kang at Morgan State University, provides a unified framework for understanding how these materials function and a clear roadmap for designing more robust and efficient filters to tackle global water contamination.

Biochar, a carbon-rich material made from pyrolyzed biomass, and hydrogels, water-absorbing polymer networks, are powerful on their own. When combined, they create a synergistic adsorbent with enhanced capabilities. This review analyzes the extensive body of literature to demonstrate that the true power of these composites comes from their surface functional groups—specific chemical moieties like carboxyl, hydroxyl, and amine groups that act as molecular-scale "hooks" to capture contaminants. The hydrogel matrix not only adds its own functional groups but also makes the biochar’s reactive sites more accessible, explaining why the composite consistently outperforms its individual components.

Reservoirs are widely recognized as important sites for carbon burial, but their true potential as climate regulators has remained partially understood. A new study from Guizhou University published in Carbon Research provides a mechanistic explanation for why reservoirs in karst landscapes—regions formed from soluble rocks like limestone—are exceptionally effective carbon sinks. By tracing the journey of carbon from water to sediment, the research demonstrates that these unique ecosystems not only capture vast amounts of carbon but also lock it away in a highly stable, long-lasting form.

The investigation centered on the Songbaishan Reservoir in China, a typical system within a karst basin. These regions are characterized by water rich in dissolved inorganic carbon from rock weathering, which provides a key ingredient for aquatic photosynthesis. The research team, led by corresponding author Wanfa Wang, employed a sophisticated suite of analytical techniques, including stable isotope tracing, organic carbon fractionation, and high-resolution mass spectrometry, to build a complete picture of the reservoir's carbon cycle. This allowed them to quantify how much carbon was produced internally versus washed in from land and to determine its ultimate fate in the sediment.

The Karst Advantage

A central finding is the powerful role of the biological carbon pump (BCP), a process where phytoplankton convert dissolved carbon into organic matter. During the warm season, the reservoir's water column becomes thermally stratified, creating ideal conditions for algal blooms in the sunlit upper layer. This supercharged BCP consumes enormous amounts of dissolved inorganic carbon, generating a massive pool of autochthonous organic carbon (AOC)—carbon produced within the reservoir itself. This internal production supports a remarkably high organic carbon burial rate of 89.5 g C m⁻² a⁻¹, significantly higher than rates in many non-karst reservoirs.