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Abstract Rancid animal fats unsuitable for human or animal food production represent low‐value and abundant, yet underexploited organic chemical precursors. The current work describes a strategy to synthesize high sulfur‐content materials (HSMs) that directly utilizes a blend of partially hydrolyzed chicken fat and plant oils as the organic comonomers, following up on analogous reactions using brown grease in place of chicken fat. The reaction of sulfur and chicken fat with either canola or sunflower oil yielded crosslinked polymer composites CFSxor GFSx, respectively (x = wt% sulfur, varied from 85%–90%). The composites exhibited compressive strengths of 24.7–31.7 MPa, and flexural strengths of 4.1–5.7 MPa, exceeding the value of established construction materials like ordinary Portland cement (compressive strength ≥17 MPa required for residential building, flexural strength 2–5 MPa). The composites also exhibited thermal stability up to 215–224 °C. The simple single‐step protocol described herein represents a way to upcycle an affordable and previously unexploited animal fat resource to form structural composites via the atom economical inverse vulcanization mechanism.
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This content will become publicly available on June 15, 2026
Brown Grease Esterification: A Design Strategy to Modulate Homogeneity, Cross‐Linking, and Upcycled Mass Economy in High Sulfur‐Content Materials
ABSTRACT Brown grease (BG) is a high‐free fatty acid (FFA) waste coproduct from the food industry that remains largely unexploited. Herein, we describe a design strategy to upcycle BG into high sulfur‐content materials (HSMs) via inverse vulcanization, circumventing the need for costly transition metals or food‐grade compatibilizers. First, BG was esterified with methyl or allyl groups, yielding MeBG and aBG, respectively. This modification masked the polar carboxylic acids and enhanced miscibility with molten sulfur. Subsequent inverse vulcanization produced remeltable HSMs at 80 or 90 wt% sulfur with uniform elemental distributions by SEM–EDX. FT‐IR spectroscopy revealed the consumption of C=C moieties and the formation of C–S bonds, signifying robust cross‐linking. Thermal analysis (TGA, DSC) indicated good thermal stability (Td,5%up to 223°C) and glass transitions characteristic of polysulfide networks. Mechanical evaluations demonstrated compressive strengths up to 19.2 MPa, exceeding the minimum requirement for residential foundation‐grade cement (17 MPa) and rivaling previously reported HSMs containing similarly high sulfur content. Notably, MeBG and aBG incorporate organics comprising up to 97 wt% BG, significantly improving the upcycled mass efficiency relative to earlier BG‐based composites. This esterification‐driven approach thus offers a practical, scalable pathway to convert low‐value BG into advanced materials with tunable thermomechanical properties.
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- Award ID(s):
- 2203669
- PAR ID:
- 10650096
- Publisher / Repository:
- wiley
- Date Published:
- Journal Name:
- Journal of Polymer Science
- Volume:
- 63
- Issue:
- 12
- ISSN:
- 2642-4150
- Page Range / eLocation ID:
- 2651 to 2661
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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ABSTRACT High sulfur‐content materials (HSMs) prepared via inverse vulcanization are attractive for a range of sustainable material applications, particularly when synthesized from waste‐derived feedstocks such as brown grease (BG). Two BG‐based composites,SunBG90andaBG90, were prepared using elemental sulfur and either native or allylated brown grease, respectively. This study explores the effect of reinforcing these sulfur‐rich networks with low loadings (0.5–2 wt. %) of highcis‐1,4‐content liquid polybutadiene (PBD). Incorporation of PBD resulted in significant increases in storage modulus, with a near‐linear relationship between PBD content and stiffness enhancement for both material types. At −60°C, storage modulus increased more than fivefold foraBG90and more than tripled forSunBG90. In contrast, flexural strength and flexural modulus exhibited non‐linear responses, with diminishing or reversed gains at higher PBD loadings, suggesting limits to rubber domain compatibility and dispersion. Thermal analysis confirmed high decomposition temperatures (212°C–226°C) and stable glass transitions, indicating thermal robustness of the reinforced networks. Compared with previous studies requiring higher PBD loadings, these results demonstrate that BG‐based HSMs can be effectively reinforced at low additive levels, offering mechanically robust, low‐cost, and renewable alternatives for structural applications.more » « less
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