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Lignin is the most abundant natural source of aromatics but remains underutilized. Elemental sulfur is a plentiful by-product of fossil fuel refining. Herein we report a strategy for preparing a durable composite by the one-pot reaction of elemental sulfur and lignin oil comprising lower molecular weight lignin derivatives. A lignin oil-sulfur composite (LOS₉₀) was prepared by reacting 10 wt. % lignin oil with 90 wt. % elemental sulfur. The composite could be remelted and reshaped over several cycles without loss of properties. Results from the study showed thatLOS₉₀has properties competitive with or exceeding values for commercial ordinary Portland cement and brick formulations. For example,LOS₉₀displayed impressive compressive strength (22.1 MPa) and flexural strength (5.7 MPa).LOS₉₀is prepared entirely from waste materials with 98.5% atom economy of composite synthesis, a lowEfactor of 0.057, and lignin char as the only waste product of the process for its preparation. These results suggest the potential applications of lignin and waste sulfur in the continuous efforts to develop more recyclable and sustainable materials.

Lignocellulosic biomass remains underutilized despite its annual production in gigaton quantities. Sulfur is another vastly underutilized waste product of fossil fuel refining. New mechanistic insight into the reactions of sulfur unveiled since 2020 suggest a rich and hitherto unexplored chemistry between biomass‐derived olefins and elemental sulfur. In this study, four biomass‐derived olefins (eugenol (1), 4‐allyl‐2,6‐dimethoxyphenol (2),o‐eugenol (3), and 2‐allyl‐6‐methylphenol(4)) were reacted with elemental sulfur to elucidate the S−C bond‐forming and other reactivity of these compounds. Each of the compounds was reacted with elemental sulfur in three sulfur : organic reactant ratios (2 : 1, 4 : 1 and 9 : 1) and at two temperatures (180 °C or 230 °C). Product mixtures were characterized using¹H NMR spectrometry and GC‐MS analysis. Products resulting from a range of mechanisms were unveiled, including inverse vulcanization, S−C_{allylic/benzylic}bond formation, S−C_arylbond formation, intramolecular cyclization, C−C σ‐bond scission, and C−O σ‐bond scission. It is anticipated that the insights from this study will support further synergy between the critical sustainability goals of biomass and sulfur utilization.

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.