Sustainable Chemistry · 2024 · 17 citations · 45 references
Natural SciencesChemical EngineeringChemistryGreen ChemistryOrganic ChemistrySeparation ScienceChromatographic PurificationChromatographyExtraction TechniquesGreen Separation ProcessesLipid ChemistrySolvent ExtractionColumn ChromatographyEnergy ConsumptionExtraction Of Organic CompoundsHigh-throughput PurificationIsolationPhenolic Compound SeparationPurificationVacuum Distillation
Exploring sustainable approaches to replace petroleum-based chemicals is an ongoing challenge in reducing the carbon footprint. Due to the complexity and percentage variation in nature-generated molecules, which further varies based on geographical origin and the purification protocol adopted, a better isolation strategy for individual components is required. Agrowaste from the cashew industry generates phenolic lipid (cardanol)-rich cashew nutshell liquid (CNSL) and has recently shown extensive commercial utility. Cardanol naturally exists as a mixture of three structurally different components with C15-alkylene chains: monoene, diene, and triene. The separation of these three fractions has been a bottleneck and is crucial for certain structural designs and reproducibility. Herein, we describe the gram-scale purification of cardanol into each component using flash column chromatography within the sustainability framework. The solvent used for elution is recovered and reused after each stage (up to 82%), making it a cost-effective and sustainable purification strategy. This simple purification technique replaces the alternative high-temperature vacuum distillation, which requires substantial energy consumption and poses vacuum fluctuation and maintenance challenges. Three components (monoene 42%, diene 22%, and triene 36%) were isolated with good purity and were fully characterized by 1H and 13C NMR, GC-MS, HPLC, and FTIR spectroscopy. The present work demonstrates that greener and simpler strategies pave the way for the isolation of constituents from nature-sourced biochemicals and unleash the potential of CNSL-derived fractions for high-end applications.
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Synthetic strogenic Agents without the Phenanthrene Nucleus
E. C. Dodds, Wilfrid Lawson · Nature · 1936 · 606 citations
Naturally occurring phenolic sources: monomers and polymers
Bimlesh Lochab, Swapnil Shukla, I. K. Varma · RSC Advances · 2014 · 285 citations