scholarly journals Mineralization, kinetics, and degradation pathway of pentachlorophenol degradation from aqueous media via persulfate/dithionite process

2021 ◽  
pp. 103357
Author(s):  
Ghorban Asgari ◽  
Abdolmotaleb Seid-Mohammadi ◽  
Mohammad Reza Samargandi ◽  
Reza Jamshidi
Keyword(s):  
Aqueous Media ◽  
Degradation Pathway ◽  
Mineralization Kinetics

Efficient removal of diuretic hydrochlorothiazide from water by electro-Fenton process using BDD anode: a kinetic and degradation pathway study

2019 ◽  
Vol 16 (8) ◽  
pp. 613 ◽  
Author(s):  
Hélène Monteil ◽  
Nihal Oturan ◽  
Yoan Péchaud ◽  
Mehmet A. Oturan
Keyword(s):  
Electrochemical Oxidation ◽  
Oxidation Reaction ◽  
Oxidation Process ◽  
Aqueous Media ◽  
Degradation Pathway ◽  
Constant Current ◽  
Gas Chromatography Mass Spectrometry ◽  
Aqueous Environment ◽  
Fenton Process ◽  
Kinetic Rate Constant

Environmental contextHydrochlorothiazide, a common diuretic pharmaceutical, occurs in environmental waters because current treatment technologies are unable to eliminate it from wastewater. To remove this environmentally hazardous chemical from water, we developed an advanced electrochemical oxidation process to efficiently degrade and mineralise the compound. Wider application of the process holds the promise of general, efficient destruction of pharmaceuticals in aqueous media. AbstractThe degradation and the mineralisation of the diuretic hydrochlorothiazide were studied by an advanced electrochemical oxidation process, ‘electro-Fenton’, which generates in situ hydroxyl radicals that are able to successfully oxidise or mineralise organic pollutants. In this study, a 0.1mM (29.8mgL−1) hydrochlorothiazide solution was completely oxidatively degraded in 15min under constant current electrolysis at 500 mA. The absolute kinetic rate constant of the oxidation reaction was also determined as (4.37±0.04)×109M−1s−1. The quasi-complete mineralisation of the solution was obtained with electrolysis for 6h under the same applied current. Several oxidation reaction intermediates were identified using gas chromatography-mass spectrometry (GC-MS). The formed carboxylic acids during the mineralisation process were also studied; oxamic, oxalic, acetic and maleic acids were identified and their concentrations were monitored throughout the electrolysis. The ions released during the treatment were also considered. Based on these data and the total organic carbon (TOC) removal results, a possible mineralisation pathway was proposed. These findings enable the conclusion that the electro-Fenton process is an efficient and environmentally-friendly method to eliminate the hazardous drug hydrochlorothiazide from an aqueous environment.

scholarly journals Degradation rates and products of pure magnesium exposed to different aqueous media under physiological conditions

2016 ◽  
Vol 17 (3-4) ◽  
Author(s):  
Marc Kieke ◽  
Frank Feyerabend ◽  
Jacques Lemaitre ◽  
Peter Behrens ◽  
Regine Willumeit-Römer
Keyword(s):  
Aqueous Media ◽  
In Vitro Study ◽  
Degradation Pathway ◽  
Culture Conditions ◽  
Pure Magnesium ◽  
Physiological Conditions ◽  
Degradation Rates ◽  
Biomaterial Science

AbstractAs magnesium and many of its alloys are a promising class of degradable implant materials, a thorough understanding of their degradation under physiological conditions is a key challenge in the field of biomaterial science. In order to increase the predictive power of in vitro studies, it is necessary to imitate the in vivo conditions, track the decomposition process and identify the products that form during the degradation pathway. In this in vitro study, slices of pure magnesium were exposed to Hank’s Balanced Salt Solution (HBSS), Dulbecco’s Modified Eagle Medium (DMEM) and simulated body fluid (SBF), respectively, under cell culture conditions, which included CO

scholarly journals Correlation between degradation pathway and toxicity of acetaminophen and its by-products by using the electro-Fenton process in aqueous media

Chemosphere ◽  
2017 ◽  
Vol 172 ◽  
pp. 1-9 ◽  
Author(s):  
Thi Xuan Huong Le ◽  
Thi Van Nguyen ◽  
Zoulkifli Amadou Yacouba ◽  
Laetitia Zoungrana ◽  
Florent Avril ◽  
...  
Keyword(s):  
Aqueous Media ◽  
Degradation Pathway ◽  
Fenton Process ◽  
By Products

Highly efficient and selective photocatalytic CO2 to CO conversion in aqueous solution

2020 ◽  
Vol 56 (27) ◽  
pp. 3851-3854 ◽  
Author(s):  
Xiaomin Chai ◽  
Hai-Hua Huang ◽  
Huiping Liu ◽  
Zhuofeng Ke ◽  
Wen-Wen Yong ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photocatalytic Performance ◽  
Aqueous Media ◽  
Highly Efficient ◽  
Co Conversion

A Co-based complex displayed the highest photocatalytic performance for CO2 to CO conversion in aqueous media.

Detection of a covalent-ionic carbinolamine intermediate in aqueous media by SDTLC on silica gel plates

2007 ◽  
Vol 20 (3) ◽  
pp. 227-230 ◽  
Author(s):  
Ana Reverdito ◽  
Mariano García ◽  
Alejandra Salerno ◽  
Oscar Locani ◽  
Isabel Perillo
Keyword(s):  
Silica Gel ◽  
Aqueous Media

Temperature Dependence of the Self-Assembled Styrene Based Random Ionomers in Aqueous Solution

2003 ◽  
Vol 775 ◽  
Author(s):  
Sung-Hwa Oh ◽  
Ju-Myung Song ◽  
Joon-Seop Kim ◽  
Hyang-Rim Oh ◽  
Jeong-A Yu
Keyword(s):  
Partition Coefficients ◽  
Room Temperature ◽  
Aqueous Media ◽  
The Self ◽  
Spectroscopic Methods ◽  
Ion Content ◽  
Repeat Units ◽  
Notable Effect ◽  
Order Of Magnitude ◽  
Experimental Errors

AbstractSolution behaviors of poly(styrene-co-sodium methacrylate) were studied by fluorescence spectroscopic methods using pyrene as a probe. The mol% of methacrylate was in the range 3.6–9.4. Water and N,N-dimethylforamide(DMF) mixture was used as a solvent (DMF/water = 0.2 mol %). The critical micelle (or aggregation) concentrations of ionomers and the partition coefficients of pyrene were obtained the temperature range 10–80°C. At room temperature, the values of CMCs (or CACs) were in the range 4.7 ×10-6 5.3 ×10-6 g/mL and we could not find any notable effect of the content of ionic repeat units within the experimental errors. Unlike CMCs, as the ion content increased, partitioning of pyrene between the hydrophobic aggregates and an aqueous media decreased from 1.5 ×105 to 9.4 ×104. As the temperature increased from 10 to 80 °C, the values of CMCs increased less than one order of magnitude. While, the partition coefficients of pyrene decreased one order of magnitude and the effect of the ion content became negligible.

Host-Guest Interactions on Electrode Surfaces for Immobilization of Molecular Catalysts

2020 ◽  
Author(s):  
Laurent Sévery ◽  
Jacek Szczerbiński ◽  
Mert Taskin ◽  
Isik Tuncay ◽  
Fernanda Brandalise Nunes ◽  
...  
Keyword(s):  
Aqueous Media ◽  
Heterogeneous Systems ◽  
Catalytic Systems ◽  
New Approach ◽  
Molecular Systems ◽  
Electrode Surfaces ◽  
Catalytic Surfaces ◽  
Oxide Electrodes ◽  
The Stability ◽  
Molecular Catalysts

The strategy of anchoring molecular catalysts on electrode surfaces combines the high selectivity and activity of molecular systems with the practicality of heterogeneous systems. The stability of molecular catalysts is, however, far less than that of traditional heterogeneous electrocatalysts, and therefore a method to easily replace anchored molecular catalysts that have degraded could make such electrosynthetic systems more attractive. Here, we apply a non-covalent “click” chemistry approach to reversibly bind molecular electrocatalysts to electrode surfaces via host-guest complexation with surface-anchored cyclodextrins. The host-guest interaction is remarkably strong and allows the flow of electrons between the electrode and the guest catalyst. Electrosynthesis in both organic and aqueous media was demonstrated on metal oxide electrodes, with stability on the order of hours. The catalytic surfaces can be recycled by controlled release of the guest from the host cavities and readsorption of fresh guest. This strategy represents a new approach to practical molecular-based catalytic systems.

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