The recovery of copper and other valuable metals had become increasingly strategic for the future of the global economy, particularly in regions lacking abundant mineral resources, such as most European countries. In this study, we investigated the viability of utilizing environmentally friendly, cost-effective, abundant and bio-based ligands, specifically carboxylic acids and their derivatives, for copper leaching in a low-temperature hydrometallurgical process. Our investigation focused on elucidating the impact of substituents in the α position of hydroxy-carboxylic acids on copper solubilization efficacy. Notably, hydroxy-carboxylic acids, like malic acid and lactic acid, were evidenced as particularly promising ligands for leaching copper from a custom-made multimetallic powder. By thoroughly characterizing the obtained complexes (Raman, UV-Vis) and by supporting the experimental efforts by a Design of Experiment (DoE) approach, we optimized the leaching process. The influence of experimental parameters such as pH, temperature, leaching time, and Cu/ligand molar ratio on process yield (determined through Inductively Coupled Plasma - Optical Emission Spectroscopy, ICP-OES, analysis) was thoroughly investigated. Additionally, we developed a subsequent copper recovery step by precipitating copper (II) hydroxide in an alkaline environment, guided by speciation diagrams tailored for each copper-ligand system.
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http://dx.doi.org/10.1002/cssc.202401389 | DOI Listing |
ChemSusChem
January 2025
Department of Chemical Sciences, University of Padova, Via Francesco Marzolo 1, 35131, Padova, Italy.
The recovery of copper and other valuable metals had become increasingly strategic for the future of the global economy, particularly in regions lacking abundant mineral resources, such as most European countries. In this study, we investigated the viability of utilizing environmentally friendly, cost-effective, abundant and bio-based ligands, specifically carboxylic acids and their derivatives, for copper leaching in a low-temperature hydrometallurgical process. Our investigation focused on elucidating the impact of substituents in the α position of hydroxy-carboxylic acids on copper solubilization efficacy.
View Article and Find Full Text PDFChem Sci
July 2024
Department of Pharmacy-Drug Sciences, Flow Chemistry and Microreactor Technology FLAME-Lab University of Bari "A. Moro" Via E. Orabona 4 70125 Bari Italy
Naturally occurring and readily available α-hydroxy carboxylic acids (AHAs) are utilized as platforms for visible light-mediated oxidative CO-extrusion furnishing α-hydroxy radicals proved to be versatile C1 to C hydroxyalkylating agents. The direct decarboxylative Giese reaction (DDGR) is operationally simple, not requiring activator or sacrificial oxidants, and enables the synthesis of a diverse range of hydroxylated products, introducing connectivity typically precluded from conventional polar domains. Notably, the methodology has been extended to widely used glycolic acid resulting in a highly efficient and unprecedented C1 hydroxyhomologation tactic.
View Article and Find Full Text PDFBioresour Technol
September 2024
Department of Chemical Engineering, State University of New York College of Environmental Science and Forestry, Syracuse, NY 13210, United States.
A novel ternary deep eutectic solvent (TDES), consisting of zinc chloride, ethylene glycol and alpha hydroxy carboxylic acids (i.e., glycolic acid, citric acid and malic acid), was first proposed to effectively fractionate and convert willow (Salix matsudana cv.
View Article and Find Full Text PDFBioresour Bioprocess
January 2024
School of Biological Sciences and Biotechnology, Graduate School, Chonnam National University, Gwangju, Republic of Korea.
The bioconversion of 4-hydroxy-2-keto acid derivatives via aldol condensation of formaldehyde and pyruvate has received substantial attention as potential source of chemicals for production of amino acids, hydroxy carboxylic acids, and chiral aldehydes. We developed an environmentally friendly biocatalyst consisting of a novel thermostable class II pyruvate aldolase from Deinococcus radiodurans with maltose-binding protein (MBP-DrADL), which has specific activity of 46.3 µmol min mg.
View Article and Find Full Text PDFPharmaceutics
February 2024
Life Sciences, Pharmacy and Chemistry, HSSCE Faculty, Kingston University, Kingston upon Thames KT1 2EE, UK.
With direct application to current and future consumer healthcare products, this research sheds light on the importance of packaging and its potential effects on both Active Pharmaceutical Ingredient (API) delivery and stability. Industrially sourced, proprietary experimental formulations (PEFs), specifically oral cleansers, based on salicylic acid and hydrogen peroxide, discolored over time at different rates, depending on packaging type used. This discoloration stemmed from an interplay of two factors, involving both spontaneous formulation degradation and the interaction of both degradants and salicylic acid with the internal surface of the packaging.
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