Because of various negative impacts of chromium intensive manufacturing, the leather-based fashion industry is under pressure to use environmentally friendly tanning technologies. However, there is a lack of scientific research that evaluates the environmental impacts of novel tanning processes. Thus, this study is aimed to quantify and compare the environmental impacts of traditional chromium-based process and a novel metal-free tanning technology. The novel metal-free technology is based on synthetic tannins, instead of metal or vegetable-based tannins. To achieve the objectives, a detailed life cycle assessment was done for 1 m of finished leather. The primary data were gathered from two different leather manufacturing plants located in the same Italian municipality and the background data were extracted from the Ecoinvent database. SimaPro 9.4 was used as the modeling software tool, and the impacts were evaluated for midpoint impact categories. For the novel metal-free tanning technology, the results revealed a significant reduction in various impact categories, such as particulate matter impacts were reduced by 25%, human toxicity (non-carcinogenic) by 31%, human toxicity (carcinogenic) by 56%, and acidification by 29%. Overall, based on single point performance score, the novel metal-free tanning system showed 18.4% less environmental impacts than the chrome-based tanning. For the most relevant impact categories, the novel metal-free tanning system again showed significantly less impact. The cattle breeding phase contributed most to various relevant impact categories, including acidification, particulate matter, and terrestrial eutrophication. Two alternative scenarios were also developed and evaluated to show how the solar energy may help further reduce the environmental impacts. A sensitivity analysis was also carried out to see the influence of uncertainty linked with the choice of thermal energy source. Overall, the study highlighted how the green tanning technologies and green energy initiatives could help decarbonize and improve the environmental performance of leather manufacturing industry.
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http://dx.doi.org/10.1007/s11356-024-35625-4 | DOI Listing |
Acc Chem Res
January 2025
Department of Chemistry and Chemistry Institution for Functional Materials, Pusan National University, Busan 46241, Republic of Korea.
ConspectusControlling selectivity through manipulation of reaction intermediates remains one of the most enduring challenges in organic chemistry, providing novel solutions for selective C-C π-bond functionalization. This approach, guided by activation principles, provides an effective method for selective functional group installation, enabling direct synthesis of organic molecules that are inaccessible through conventional pathways. In particular, the selective functionalization of N-conjugated allenes and alkynes has emerged as a promising research focus, driven by advances in controlling reactive intermediates and activation strategies.
View Article and Find Full Text PDFJ Org Chem
January 2025
Evotec (US) Inc., 303B College Road East, Princeton, New Jersey 08540, United States.
A novel, highly diastereoselective, and metal-free synthesis of multisubstituted piperidines via an S1 approach is reported in this study. The method allows for the preparation of highly functionalized compounds with exceptional diastereomeric selectivities and consistently reproducible yields. These compounds are of significant interest due to their remarkable biological activities toward influenza endonuclease.
View Article and Find Full Text PDFLangmuir
January 2025
Department of Chemistry, Faculty of Science, Ilam University, P.O. Box 69315516, Ilam, Iran.
Front Chem
December 2024
Faculty of Health Sciences Collegium Medicum, The Mazovian Academy in Plock, Płock, Poland.
2,3-Dihydrobenzofurans are noteworthy scaffolds in organic and medicinal chemistry, constituting the structural framework of many of the varied medicinally active organic compounds. Moreover, a diverse variety of biologically potent natural products also contain this heterocyclic nucleus. Reflecting on the wide biological substantiality of dihydrobenzofurans, several innovative and facile synthetic developments are evolving to achieve these heterocycles.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Organocatalysis Research Group, Institute of Organic Chemistry, HUN-REN Research Centre for Natural Sciences, Magyar tudósok körútja 2, Budapest H-1117, Hungary.
The partial reduction of esters to aldehydes is a fundamentally important transformation for the synthesis of numerous fine chemicals and consumer goods. However, despite the many efforts, limitations have persisted, such as competing overreduction, low reproducibility, use of exigent reaction conditions and hazardous chemicals. Here, we report a novel catalyst family with a unique steric design which promotes the catalytic partial reduction of esters with unprecedented, near-perfect selectivity and efficiency.
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