Iridium nanoparticles with high catalytic activity in degradation of acid red-26: an oxidative approach

2016 ◽  
Vol 74 (11) ◽  
pp. 2551-2559 ◽  
Author(s):  
Anjali Goel ◽  
Rajni Lasyal

Nanocatalysis using metal nanoparticles constitutes one of the emerging technologies for destructive oxidation of organics such as dyes. This paper deals with the degradation of acid red-26 (AR-26), an azo dye by hexacyanoferrate (abbreviated as HCF) (III) using iridium nanoparticles. UV-vis spectroscopy has been employed to obtain the details of the oxidative degradation of the selected dye. The effect of various operational parameters such as HCF(III) concentration, pH, initial dye concentration, catalyst and temperature was investigated systematically at the λmax, 507 nm, of the reaction mixture. Degradation kinetics follows the first order kinetic model with respect to AR-26 and Ir nano concentrations, while with respect to the HCF(III) concentration reaction it follows first order kinetics at lower concentrations, tending towards zero order at higher concentrations. Thermodynamic parameters have been calculated by studying the reaction rate at four different temperatures. The UV-vis, high performance liquid chromatography (HPLC), liquid chromatography–mass spectrometry (LC-MS) analysis of degradation products showed the formation of carboxylic acid and substituted carboxylic acids as major degradation products, which are simple and less hazardous compounds. The big advantage of the present method is the recovery and reuse of iridium nanoparticles. Moreover, turnover frequencies for each catalytic cycle have been determined, indicating the long life span of Ir nanoparticles. Thus, the finding is a novel and highly economical alternative for environmental safety against pollution by dyes, and extendable for other contaminants as well.

2012 ◽  
Vol 65 (12) ◽  
pp. 2175-2182
Author(s):  
Abeer S. Elsherbiny ◽  
Sahar H. El-Khalafy ◽  
Michael P. Doyle

The kinetics of the oxidative degradation of an azo dye Metanil Yellow (MY) was investigated in aqueous solution using dirhodium(II) caprolactamate, Rh2(cap)4, as a catalyst in the presence of H2O2 as oxidizing agent. The reaction process was followed by UV/Vis spectrophotometer. The decolorization and degradation kinetics were investigated and both followed a pseudo-first-order kinetic with respect to the [MY]. The effects of various parameters such as H2O2 and dye concentrations, the amount of catalyst and temperature have been studied. The studies show that Rh2(cap)4 is a very effective catalyst for the formation of hydroxyl radicals HO• which oxidized and degraded about 92% of MY into CO2 and H2O after 24 h as measured by total carbon analyzer.


2012 ◽  
Vol 77 (12) ◽  
pp. 1747-1757 ◽  
Author(s):  
Veljko Djokic ◽  
Jelena Vujovic ◽  
Aleksandar Marinkovic ◽  
Rada Petrovic ◽  
Djordje Janackovic ◽  
...  

The photocatalytic degradation of synthetic textile dye CI Basic Yellow 28 (BY28) in water, using recently synthesized P160 TiO2 based catalyst, under Osram ultra-vitalux? lamp (300 W) light, was studied. The effect of the operational parameters such as initial concentration of catalyst, initial dye concentration and pH was studied. Salt effect was also investigated (NaCl, Na2CO3, Na2SO4, NaNO3). It was found that the optimal concentration of catalyst is 2.0 g L-1. A pseudo first-order kinetic model was illustrated using the Langmuir-Hinshelwood mechanism, and the adsorption equilibrium constant and the rate constant of the surface reaction were calculated (KBY = 6.126 L mg-1 and kC = 0.272 mg L-1 min-1, respectively). The photodegradation rate was higher in weak acidic than in high acidic and alkaline conditions. The presence of CO32- ions increases the photodegradation rate while Cl-, SO42- and NO3-ions decreases the reaction rate. The rate of photodegradation of BY28 was measured using UV-Vis spectroscopy.


2019 ◽  
Vol 2019 ◽  
pp. 1-10 ◽  
Author(s):  
Juanjuan Zhao ◽  
Yujiao Sun ◽  
Fachao Wu ◽  
Minjian Shi ◽  
Xurui Liu

Antibiotic residues and antibiotic resistance genes (ARGs) pose a great threat to public health and food security via the horizontal transfer in the food production chain. Oxidative degradation of amoxicillin (AMO) in aqueous solution by thermally activated persulfate (TAP) was investigated. The AMO degradation followed a pseudo-first-order kinetic model at all tested conditions. The pseudo-first-order rate constants of AMO degradation well-fitted the Arrhenius equation when the reaction temperature ranged from 35°C to 60°C, with the apparent activate energy of 126.9 kJ·mol−1. High reaction temperature, high initial persulfate concentration, low pH, high Cl− concentration, and humic acid (HA) concentration increased the AMO degradation efficiency. The EPR test demonstrated that both ·OH and SO4·− were generated in the TAP system, and the radical scavenging test identified that the predominant reactive radical species were SO4·− in aqueous solution without adjusting the solution pH. In groundwater and drinking water, AMO degradation suggested that TAP could be a reliable technology for water remediation contaminated by AMO in practice.


2009 ◽  
Vol 92 (1) ◽  
pp. 138-147 ◽  
Author(s):  
Sunil R Dhaneshwar ◽  
Mahadeo V Mahadik ◽  
Mahesh J Kulkarni

Abstract The objective of this work was to study the degradation behavior of escitalopram oxalate under different International Conference on Harmonization (ICH)-recommended stress conditions by column liquid chromatography (LC)-UV and LC/mass spectrometry (LC/MS) and to establish a validated stability-indicating LC assay method. Escitalopram oxalate was subjected to stress conditions of hydrolysis, oxidation, photolysis, and thermal decomposition. Extensive degradation was found to occur in alkaline medium. Mild degradation was observed in acidic and oxidative conditions. Escitalopram oxalate was stable to neutral, photolytic, and thermal stress. Successful separation of the drug from degradation products formed under stress conditions was achieved on a PerfectSil-100 ODS-3 column [C18 (5 m, 25 cm 4.6 mm id)] using methanol0.01 M acetate buffer pH 3.8 adjusted with acetic acid (45 + 55) as the mobile phase. The flow rate was 1 mL/min, and the detection wavelength was 239 nm. The method was validated according to ICH guidelines. Major degradation products formed in hydrolysis and oxidative conditions were isolated, and structural elucidation of degradation products was done by LC/MS and infrared spectrometry studies. The major hydrolysis degradation product was confirmed as 1-(3-dimethylaminopropyl)-1-(4-fluoro- phenyl)-1,3dihydroisobenzofuran-5-carboxylic acid, and the major oxidative degradation product was confirmed as 1-{[3-dimethylamino(oxide)- propyl]-1-(4-fluro-phenyl)}-1,3-dihydro-isobenzofuran- 5-carbonitrile.


2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Vishnu P. Choudhari ◽  
Anna Pratima G. Nikalje

Factorial design tool applied for development of isocratic reversed-phase stability-indicating HPLC method for the analysis of mycophenolate mofetil (MMF) and its degradation products. MMF stress degradation products mycophenolate acid (MPA) and DP3 (USP impurity H) were isolated and used for quantitation. Separation achieved on a Symmetry C18 (250 mm × 4.6 mm, 5.0 μ) column using a methanol: acetate buffer (75 : 25 v/v), pH 6.0 (adjusted with acetic acid), at 0.5 mL flow rate, column maintained at 55°C, and data integrated at 251 nm. MMF is subjected to hydrolysis, oxidation, heat degradation, and so forth; under all these conditions degraded products are well separated. The method validation characteristics included accuracy, precision, linearity, range, specificity, and sensitivity. Robustness testing is conducted to evaluate the effect of minor changes to the chromatographic conditions and to establish appropriate system suitability parameters. The proposed method is used to investigate kinetics of acid, alkali hydrolysis and oxidation process. Major degradation products MPA and DP3 were isolated and quantitated. Characterization of MPA by NMR and LC-MS/MS and other degraded products by LC-MS/MS is attempted successfully. The method is used successfully for the quality assessment of three MMF drug commercial formations and its acid, alkali, and oxidative degradation kinetics study.


1989 ◽  
Vol 62 (5) ◽  
pp. 779-787
Author(s):  
M. S. Sambhi

Abstract The first-order and zero-order kinetic models of chain scission, based on random chain scission processes, are critically examined. It is likely that for many practical situations, the first-order chain scission kinetics can be represented by pseudozero-order kinetic types of equations. The kinetic results indicate that chain scission of NR occurs either by a pseudofirst-order or a pseudozero-order process. The pseudozero-order chain scission kinetics of NR are in consonance with the result that chain scission involves the bimolecular reaction of peroxy radicals in the termination step of the oxidation mechanism. However, this does not preclude unambiguously other chain scission reactions. The chain scission activation energy of NR is determined with the use of expressions derived for the oxidative degradation of NR as measured in terms of Wallace plasticities.


2021 ◽  
Author(s):  
Chubraider Xavier ◽  
Bianca Rebelo Lopes ◽  
Caue Ribeiro ◽  
Eduardo Bessa Azevedo

Abstract Bisphenol A (BPA), a common polymer plasticizer, is a contaminant of emerging concern with endocrine disrupting activity. Among existing abatement methods, photodegradation demands easily fabricated, inexpensive, high photoactive catalysts, leading to non-toxic byproducts after degradation. It is proposed an optimized (surface response methodology) catalyst for those goals: graphitic carbon nitride impregnated with reduced graphene oxide. The method was based on the sonication of preformed particles followed by reduction with hydrazine in reflux, a methodology that allows for better reproducibility and larger specific surface areas. The catalyst removed 90% of BPA (100 mL, 100 µg L− 1) in 90 min under UV irradiation (365 nm, 26 W) compared to 50% with pure g-C3N4 (pseudo-first-order kinetics). Tests with radicals scavengers revealed that superoxide radical was the main oxidation agent in the system. By mass spectrometry, two major degradation products were identified, which were less ecotoxic than BPA towards a series of organisms, according to in silico estimations performed with the ECOSAR 2.0 software.


Chemija ◽  
2021 ◽  
Vol 32 (1) ◽  
Author(s):  
Edita Sodaitienė ◽  
Danutė Kaušpėdienė ◽  
Audronė Gefenienė ◽  
Vladas Gefenas ◽  
Romas Ragauskas ◽  
...  

Oxidative degradation of metal complex dye Sanodure Green (SG) in the presence of H2O2 and nanostructured catalyst CuO prepared from copper plating effluents has been investigated. The activity of the CuO catalyst in the oxidative degradation reaction depended on the SG concentration, reaction time and temperature. The reaction followed a pseudo-first order kinetic model, and the rate constant was highly dependent on the increase in temperature, but only slightly on the SG concentration. Thermodynamic studies have shown that the degradation reaction of SG is endothermic. The use of copper plating effluents for the preparation of nanostructured catalyst CuO makes it possible to avoid the accumulation of difficult-to-recycle copper oxide sludge formed during effluent neutralization, and to manage copper plating and aluminum dyeing effluents more economically.


Author(s):  
Chen-Yan Hu ◽  
Si-Cheng Ren ◽  
Yi-Li Lin ◽  
Ji-Chen Zhang ◽  
Ye-Ye Zhu ◽  
...  

Abstract In this study, we studied the degradation kinetics of a common iodine contrast agent, diatrizoate, by ozone and the formation of disinfection by-products (DBPs) in the sequential chlorination. Effects of ozone concentration, solution pH, and bromide concentration on diatrizoate degradation were evaluated. The results indicate that diatrizoate can be effectively degraded (over 80% within 1 h) by ozone, and the degradation kinetics can be well described using the pseudo-first-order kinetic model. The pseudo-first-order rate constant (kobs) of diatrizoate degradation significantly increased with increasing ozone concentration and decreasing bromide concentration. The kobs kept increasing with the increase of pH value and reached a maximum of 6.5 (±0.05) × 10−2 min−1 at pH 9. As the ozone concentration gradually increased from 0.342 to 1.316 mg/L, the corresponding kobs of diatrizoate degradation increased from 1.76 (±0.20) × 10−3 to 4.22 (±0.3) × 10−2 min−1. The bromide concentration exhibited a strong inhibitory effect on diatrizoate degradation because of the competition for ozone with diatrizoate. Trichloromethane was the only detected DBP in the subsequent chlorination in the absence of bromide. However, in the presence of bromide, six other DBPs were detected, and bromochloroiodomethane and tribromomethane became the major products with concentrations 1–2 orders higher than those of the other DBPs. In order to provide safe drinking water to the public, water should be maintained at circumneutral pH values and low bromine concentrations (<5 μM) before reaching the chlorine disinfection process to effectively control the formation of DBPs.


Molecules ◽  
2019 ◽  
Vol 24 (24) ◽  
pp. 4430
Author(s):  
Anna Gumieniczek ◽  
Anna Berecka-Rycerz ◽  
Tomasz Mroczek ◽  
Krzysztof Wojtanowski

Firstly, metformin and repaglinide were degraded under high temperature/humidity, UV/VIS light, in different pH and oxidative conditions. Secondly, a new validated LC-UV method was examined, as to whether it validly determined these drugs in the presence of their degradation products and whether it is suitable for estimating degradation kinetics. Finally, the respective LC-MS method was used to identify the degradation products. In addition, using FT-IR method, the stability of metformin and repaglinide was scrutinized in the presence of polyvinylpyrrolidone (PVP), mannitol, magnesium stearate, and lactose. Significant degradation of metformin, following the first order kinetics, was observed in alkaline medium. In the case of repaglinide, the most significant and quickest degradation, following the first order kinetics, was observed in acidic and oxidative media (0.1 M HCl and 3% H2O2). Two new degradation products of metformin and nine new degradation products of repaglinide were detected and identified when the stressed samples were examined by our LC-MS method. What is more, the presence of PVP, mannitol, and magnesium stearate proved to affect the stability of metformin, while repaglinide stability was affected in the presence of PVP and magnesium stearate.


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