The global production and consumption of plastics has increased at an alarming rate over the last few decades. The accumulation of pervasive and persistent waste plastic has concomitantly increased in landfills and the environment. The societal, ecological, and economic problems of plastic waste/pollution demand immediate and decisive action. In 2015, only 9% of plastic waste was successfully recycled in the United States. The major current recycling processes focus on the mechanical recycling of plastic waste; however, even this process is limited by the sorting/pretreatment of plastic waste and degradation of plastics during the process. An alternative to mechanical processes is chemical recycling of plastic waste. Efficient chemical recycling would allow for the production of feedstocks for various uses including fuels and chemical feedstocks to replace petrochemicals. This review focuses on the most recent advances for the chemical recycling of three major polymers found in plastic waste: PET, PE, and PP. Commercial processes for recycling hydrolysable polymers like polyesters or polyamides, polyolefins, or mixed waste streams are also discussed.

Interest in starch‐based films has increased precipitously in response to a growing demand for more sustainable and environmentally sourced food packaging materials. Starch is an optimal candidate for these applications given its ability to form thermoplastic materials and films with affordable and often sustainably sourced plasticizers like those produced as waste byproducts by biodiesel and agricultural industries. Starch is also globally ubiquitous, affordable, and environmentally benign. Although the process of producing starch films is relatively straightforward, numerous factors, including starch source, extraction method, film formulation, processing methods, and curing procedures, drastically impact the ultimate material properties. The significant strides made from 2015 to early 2020 toward elucidating how these variables can be leveraged to improve mechanical and barrier properties as well as the implementation of various additives or procedural modifications are cataloged in this review. Advances toward the development of functional films containing antioxidant, antibacterial, or spoilage indicating components to prevent or signal the degradation of food products are also discussed.

Lignin is the second-most abundant biopolymer in nature and remains a severely underutilized waste product of agriculture and paper production. Sulfur is the most underutilized byproduct of petroleum and natural gas processing industries. On their own, both sulfur and lignin exhibit very poor mechanical properties. In the current work, a strategy for preparing more durable composites of sulfur and lignin, LS_x, is described. Composites LS_x were prepared by reaction of allyl lignin with elemental sulfur, whereby some of the sulfur forms polysulfide crosslinks with lignin to yield a three-dimensional network. Even relatively small quantities (<5 wt%) of the polysulfide-crosslinked lignin network provides up to a 3.4-fold increase in mechanical reinforcement over sulfur alone, as measured by the storage moduli and flexural strength determined from dynamic mechanical analysis (temperature dependence and stress–strain analysis). Notably, LS_x composites could be repeatedly remelted and recast after pulverization without loss of mechanical strength. These initial studies suggest potential practical applications of lignin and sulfur waste streams in the ongoing quest towards more sustainable, recyclable structural materials.

Lignin is the most abundant aromatic biopolymer and is the sustainable feedstock most likely to supplant petroleum-derived aromatics and downstream products. Rich in functional groups, lignin is largely peerless in its potential for chemical modification towards attaining target properties. Lignin’s crosslinked network structure can be exploited in composites to endow them with remarkable strength, as exemplified in timber and other structural elements of plants. Yet lignin may also be depolymerized, modified, or blended with other polymers. This review focuses on substituting petrochemicals with lignin derivatives, with a particular focus on applications more significant in terms of potential commercialization volume, including polyurethane, phenol-formaldehyde resins, lignin-based carbon fibers, and emergent melt-processable waste-derived materials. This review will illuminate advances from the last eight years in the prospective utilization of such lignin-derived products in a range of application such as adhesives, plastics, automotive components, construction materials, and composites. Particular technical issues associated with lignin processing and emerging alternatives for future developments are discussed.

A sterically-encumbered 5,5′-distyryl-2,2′-bipyridyl derivative that enforces a 1 : 1 metal-to-ligand ratio acts as a selective turn-on sensor for Zn²⁺ in THF.

Chlorolignin can be copolymerized with sulfur in different ratios to form durable, recyclable materials.