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The decomposition of sodium dodecylbenzene sulfonate (SDBS) in water by means of ultrasound irradiation at 20kHz was investigated. Experiments were conducted at surfactant concentrations of 175, 260 and 350 mg l(-1), liquid volumes of 120, 170 and 220 ml, temperatures of 20, 30 and 45 degrees C and applied power of 40, 80 and 125 W. The extent of degradation was followed monitoring substrate and organic carbon concentrations, while hydrogen peroxide concentration was also measured; the latter is a product of water sonolysis due to hydroxyl radical recombination. 80% SDBS conversion was achieved after 120 min of sonication at 125 W and 30 degrees C; nonetheless, SDBS and its degradation intermediates proved difficult to oxidise as only about 20-25% of the initial carbon content was transformed to carbon dioxide. At the initial stages of the reaction, degradation rate appears to be only weakly dependent on the substrate concentration with the rate increasing from 3.1 to 4 mg l(-1)min(-1) with increasing concentration from 175 to 350 mg l(-1). Degradation appears to occur at the bubble-liquid interface through hydroxyl radical-mediated reactions whose role was established by performing experiments in the presence of radical scavengers, namely potassium bromide and sodium benzoate. Degradation rates increased with increasing power and decreasing temperature and volume.
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http://dx.doi.org/10.1016/j.chemosphere.2005.04.075 | DOI Listing |
ACS Synth Biol
September 2025
Molecular Microbial Physiology Group, Swammerdam Institute for Life Sciences, Faculty of Science, University of Amsterdam, Science Park 904, Amsterdam 1098 XH, The Netherlands.
Mannitol is a naturally occurring C(6) polyol with a wide range of applications in the food and pharmaceutical industry. In a previous study, mannitol production was achieved via the direct conversion of CO in sp. PCC6803.
View Article and Find Full Text PDFJ Fluoresc
August 2025
Department of Chemistry, Faculty of Science, Damietta University, Damietta, New Damietta, Egypt.
Total quantification and speciation of Fe and Fe at trace levels in aqueous environments has emerged as an imperative analytical challenge for ecological systems and public health. Implementation of wavelength-dependent spectrochemical methodologies based on formation of chromogenic Fe chelate for Fe quantification in aqueous media also remains intrinsically challenging owing to intrinsic self-absorbance, and spectral convolution. Thus, the current study reports the development of a direct and selective eco-friendly spectrofluorometric probe for Fe detection in water.
View Article and Find Full Text PDFAnal Chem
August 2025
Key Lab of Green Chem & Tech (MOE) at College of Chemistry, Sichuan University, Chengdu, Sichuan 610064, China.
Herein, the photochemical vapor generation (PVG) of platinum was studied in three kinds of media, formic acid (FA), acetic acid (AA), and propionic acid (PA). Results demonstrated that PVG of Pt was more efficient in AA, followed by PA and last by FA. Combining inductively coupled plasma mass spectrometry (ICP-MS) for its detection, a novel analytical method for trace platinum was established.
View Article and Find Full Text PDFMicrobiol Spectr
September 2025
Environmental Engineering Institute IIE-ENAC, Laboratory MICROBE, Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.
Hydrogenotrophic methanogens play a key role in anaerobic ecosystems by catalyzing the bioconversion of hydrogen (H) and carbon dioxide (CO) into methane (CH) and water. This metabolic process is the basis of biological power-to-methane (PtM) technology, a promising solution for the long-term storage of surplus renewable energy as CH. Its successful application can be improved through a deeper understanding of methanogen physiology, particularly the metabolic response to intermittent substrate supply of H or CO.
View Article and Find Full Text PDFInt J Mol Sci
July 2025
ACCESS Health International, 384 West Lane, Ridgefield, CT 06877, USA.
Protein functional effector (pfe)RNAs were introduced in 2015 as PIWI-interacting-like small noncoding (nc)RNAs and were later categorized as a novel group based on being 2'-O-methylated at their 3'-end, directly binding and affecting protein function, but not levels, and not matching known RNAs. Here, we document that human pfeRNAs match fragments of GenBank database-annotated human ncRNAs. PDLpfeRNAa matches the 3'-half fragment of a mitochondrial transfer (t)RNA, and PDLpfeRNAb matches a 28S ribosomal (r)RNA fragment.
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