Qualitative screening of reused nutrient solution (RNS) displays the presence of several organic acids. In this study, the degradation by UV/HO of three of those organic acids (benzoic (BA), phthalic acid (PhA) and succinic acid (SA)) present in RNS was investigated. The results indicated that (i) the degradation rate of BA was faster than that of PhA and SA and (ii) by increasing the contact time the degradation of all acids was improved. For example, the removal of BA increased from 83% and 91% when increasing the contact time from 90 min to 270 min in the presence of 50 mg L and UV. A maximum COD (30%) and UV (68%) removal were obtained when 200 mg L HO was applied for 90 min. No significant change was observed in terms of parameters such as PO and NO while electrical conductivity (EC) and pH were slightly changed during the oxidation process. Pseudo- first -order represented well the experimental data for the degradation of the selected organic acids in RNS (particularly for BA and PhA), exhibiting high linear correlation coefficients (R ≥ 0.96). Moreover, the results showed that the decomposition of organic acids was significantly influenced in the presence of inorganic ions in RNS. GC-MS analysis revealed the presence of several intermediate products during the oxidation process and the primary reaction pathway of benzoic acid was accordingly proposed. Finally, a bench scale cost investigation showed that low concentration HO (50 mg L) in longer time (270 min) is more cost effective than high concentration HO (200 mg L) in a shorter time (90 min).
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.scitotenv.2019.05.477 | DOI Listing |
Chemistry
January 2025
Osaka University, Institute for Open and Transdisciplinary Research Initiatives (OTRI), 1-6 Yamada-oka, 565-0871, Suita, JAPAN.
Considering the demand for organosulfur materials and the challenges associated with currently used oxidation processes, in this study, we evaluated the counter-cation of sodium chlorite (Na+ClO2-) with tetrabutylammonium chloride (Bu4N+Cl-) to synthesise tetrabutylammonium chlorite (Bu4N+ClO2-). Bu4N+ClO2- exhibited good solubility in organic solvents like chloroform (1.6 g mL-1) and ethyl acetate (0.
View Article and Find Full Text PDFEnviron Sci Technol
January 2025
National-Regional Joint Engineering Research Center for Soil Pollution Control and Remediation in South China, Guangdong Key Laboratory of Integrated Agro-environmental Pollution Control and Management, Institute of Eco-environmental and Soil Sciences, Guangdong Academy of Sciences, Guangzhou 510650, China.
Methylmercury in paddy soils poses threats to food security and thus human health. Redox-active phenolic and quinone moieties of natural organic matter (NOM) mediate electron transfer between microbes and mercury during mercury reduction. However, their role in mercury methylation remains elusive.
View Article and Find Full Text PDFChem Biodivers
January 2025
Ataturk University: Ataturk Universitesi, Pharmacognosy, Erzurum, Erzurum, TURKEY.
Boraginaceae plants, including four endemic species from Türkiye, were analyzed for organic and inorganic compositions using ICP-MS and LC-MS/MS to explore their nutritional, medicinal, and ecological significance. This study examined 18 species, identifying key elements such as sodium (87,600.359-118,049.
View Article and Find Full Text PDFOrg Lett
January 2025
Organic Chemistry Department, Faculty of Science, Autonomous University of Madrid, 28049 Madrid, Spain.
The functionalization of the C-N bond of amines is a straightforward strategy for the construction of complex scaffolds or for the late-stage functionalization of pharmaceuticals. Herein, we describe a photoredox-catalyzed strategy for the deaminative alkylation of primary amine-derived isonitriles that provides unnatural amino acid derivatives under mild conditions. The use of silacarboxylic acids as silyl radical precursors enables the generation of carbon-centered radicals that allow the construction of Csp-Csp bonds via a Giese-type addition, avoiding the undesired hydrodeamination product.
View Article and Find Full Text PDFNat Chem
January 2025
Laboratory of Advanced Materials, Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Molecular Engineering of Polymers, Collaborative Innovation Center of Chemistry for Energy Materials (2011-iChEM), College of Chemistry and Materials, Fudan University, Shanghai, P. R. China.
The synthesis of mesoporous metal-organic frameworks (meso-MOFs) is desirable as these materials can be used in various applications. However, owing to the imbalance in structural tension at the micro-scale (MOF crystallization) and the meso-scales (assembly of micelles with MOF subunits), the formation of single-crystal meso-MOFs is challenging. Here we report the preparation of uniform single-crystal meso-MOF nanoparticles with ordered mesopore channels in microporous frameworks with definite arrangements, through a cooperative assembly method co-mediated by strong and weak acids.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!