Sharif Digital Repository

The nanocomposite of zero-valent iron and delafossite CuFeO2 supported on reduced graphene oxide was synthesized for the first time to evaluate its performance as the heterogeneous catalyst toward electro-Fenton (EF) removal of catechol. X-ray diffraction, Fourier transform-infrared, scanning electron microscopy and Brunauer–Emmett–Teller (BET) were used to characterize the nanocomposite. It was found that the rhombohedral structure of CuFeO2 remained stable during the nanocomposite preparation. The BET surface area of the nanocomposite increased about 102 times in comparison with bare CuFeO2. The influence of the operating parameters was investigated. The optimum operating conditions were... 

The electrochemical oxidation of catechol in the presence of 2-thiouracil (as a nucleophile) has been studied in aqueous solutions using cyclic voltammetry and controlled-potential coulometric techniques. The results indicate that catechol participating in a 1,4 (Michael) addition reaction converts to a new thiadiazafluorenone compound. The electrochemical synthesis of this compound has been successfully performed in an undivided cell in a good yield and purity and was characterized by IR, 1H and 13C NMR, mass spectrometry and elemental analysis. © 2003 Published by Elsevier B.V  

Biosensors could be used as digital devices to measure the sample infield. Consequently, computational programming along with experimental achievements are required. In this study, a novel biosensor/artificial neural network (ANN) integrated system was developed. Poly (3,4-ethylenedioxy-thiophene)(PEDOT), graphene oxide nano-sheets (GONs) and laccase (Lac) were used to construct a biosensor. The simple and one-pot process was accomplished by electropolymerizing 3,4-ethylenedioxy-thiophene (EDOT) along with GONs and Lac as dopants on glassy carbon electrode. Scanning electron microscopy (SEM) and electrochemical characterization were conducted to confirm successful enzyme entrapment. The... 

In the present study, photo-Fenton degradation of catechol from aqueous solution was carried out using UV light and iron ions (Fe2+) as activators of persulfate (PS). Catechol degradation from solution was studied under different experimental variables such as solution pH (2.0–10.0), iron dosages (0.1–0.5 g/L), persulfate loadings (1.0–5.0 mM), initial catechol concentrations (20–100 mg/L) and scavengers (TBA and IPA). The comparative study of catechol removal showed that among the applied approaches, the order of degradation of catechol is as follows: PS/Fe2 +/UV > PS/Fe2 + > UV/PS > PS > UV. Furthermore, higher catechol degradation was observed with increasing iron dosage and PS... 

Mass transfer efficiency and catalytic reactivity are the two major hurdles for heterogeneous catalytic wet peroxide oxidation (CWPO) technologies. To address these issues, nanocomposite CuFeO2/Al2O3 was synthesized and assessed as a novel catalyst for enhanced adsorption and oxidation of anionic pollutants (catechol and reactive red 195 (RR195)) in waters. With a positive charge on the nanocomposite by introducing Al2O3, the adsorption of anionic pollutants was promoted. The surface complexation reaction on CuFeO2/Al2O3, which fits well to the Langmuir isotherm, has engined the mass transfer of pollutants to the nanocatalyst that demonstrated 96.46% and 99.75% removal of catechol and RR195... 

Natural and synthetic anion receptors are extensively employed, but the structures of their bound complexes are difficult to determine in the liquid phase. Infrared spectroscopy is used in this work to characterize the solution structures of bound anion receptors for the first time, and surprisingly only two of three hydroxyl groups of the neutral aliphatic triols are found to directly interact with Cl-. The binding constants of these triols with zero to three CF3 groups were measured in a polar environment, and KCD3CN(Cl-) = 1.1 × 106 M-1 for the tris(trifluoromethyl) derivative. This is a remarkably large value, and high selectivity with respect to interfering anions such as, Br-, NO3 -... 

Performance enhancement of supercapacitors has been recently discussed. In this paper a novel and facile procedure for functionalization of graphene with some electroactive molecules is presented. The graphene has been functionalized by catechol-based molecules, which are electroactive molecules with electrochemically reversible properties. The functionalized graphene exhibits very effective pseudocapacitor behaviorfor charge storage. For the first time, with the aim of an electrosynthesis procedure, catechol is covalently attached on graphene sheets. This attachment has been investigated by electrochemical, X-ray photoelectron spectroscopy and attenuated total reflectance methods. Catechol... 

Charge-transfer (CT) complexes formed from the reactions of 4-nitropyrocatechol (4-nCat) as an electron acceptor with four amino alcohols: 2-aminoethanol, 1-amino-2-propanol, 4-aminobutanol and N-(2-hydroxyethyl)-1,3-diaminopropane (NHEDAP) as electron donors, have been studied spectrophotometrically in H2O and H2O/EtOH at 20, 25, 30, 35 and 40 °C. The calculated values of the oscillator strength and transition moment confirm the formation of CT-complexes. The thermodynamic and spectroscopic parameters were also evaluated for the formation of CT-complexes. The equilibrium constants ranged from 9.00 to 2.20 l mol-1 (M-1). These interactions are exothermic and have relatively large standard... 

The present study concerns the electrochemical behavior of catechol and 4-methylcatechol in the presence of 2-mercapto-5-methyl-1,3,4-thiadiazole (MMT) in aqueous medium on the surface of the glassy carbon electrode by means of cyclic voltammetry and controlled-potential coulometry. The oxidation mechanism was deduced from voltammetric and spectrophotometric data. The electro-generation of quinoid intermediates and their subsequent Michael-type reaction with MMT has been investigated as a clean and convenient strategy for the synthesis of corresponding reaction products. In addition, electro-synthesis of Michael addition products has been successfully accomplished by controlled-potential... 

Aims: The metabolism of phenanthrene and anthracene by a moderate thermophilic Nocardia otitidiscaviarum strain TSH1 was examined. Methods and Results: When strain TSH1 was grown in the presence of anthracene, four metabolites were identified as 1,2-dihydroxy-1,2-dihydroanthracene, 3-(2-carboxyvinyl)naphthalene-2-carboxylic acid, 2,3-dihydroxynaphthalene and benzoic acid using gas chromatography-mass spectrometry (GC-MS), reverse phase-high performance liquid chromatography (RP-HPLC) and thin-layer chromatography (TLC). Degradation studies with phenanthrene revealed 2,2′-diphenic acid, phthalic acid, 4-hydroxyphenylacetic acid, o-hydroxyphenylacetic acid, benzoic acid, a phenanthrene... 

The thermophilic bacterium Nocardia otitidiscaviarum strain TSH1, originally isolated in our laboratory from a petroindustrial wastewater contaminated soil in Iran, grows at 50 °C on a broad range of hydrocarbons. Transformation of naphthalene by strain TSH1 which is able to use this two ring-polycyclic aromatic hydrocarbon (PAH) as a sole source of carbon and energy was investigated. The metabolic pathway was elucidated by identifying metabolites, biotransformation studies and monitoring enzyme activities in cell-free extracts. The identification of metabolites suggests that strain TSH1 initiates its attack on naphthalene by dioxygenation at its C-1 and C-2 positions to give... 

An indirect colorimetric method is presented for detection of trace amounts of hydroquinone (1), catechol (2) and pyrogallol (3). The reduction of AuCl4- to Gold nanoparticles (Au-NPs) by these phenolic compounds in the presence of cetyltrimethylammonium chloride (CTAC) produced very intense surface plasmon resonance peak of Au-NPs. The plasmon absorbance of Au-NPs allows the quantitative colorimetric detection of the phenolic compounds. The calibration curves derived from the changes in absorbance at λ = 568 nm were linear with concentration of hydroquinone, catechol and pyrogallol in the range of 7.0 × 10-7 to 1.0 × 10-4M, 6.0 × 10-6 to 2.0 × 10-4 M and 6.0 × 10-7 to 1.0 × 10-4 M,... 

The electrochemical behavior of catechol in the presence of propylthiouracil (PTU) and methylthiouracil (MTU) at a glassy carbon electrode is thoroughly investigated. The cyclic voltammetric studies of the systems are performed in different pHs and sweep rates. The results of the voltammetric foundations show an electrocatalytic oxidation of catechol in the presence of PTU and MTU, leading to a remarkable increase in the anodic peak current of catechol together with the contemporaneous disappearance of the corresponding cathodic wave. The presented mechanism shows the nucleophilic addition/reduction of the electro-generated o-quinone by the PTU or MTU, which produced chemically reduced... 

Equilibrium constants for formation of a cobalt(II) complex with the bidentate ligand dopamine have been studied with spectrophotometric methods in water + ethanol cosolvent systems at 15, 25, and 35 (±0.1)∈°C and an ionic strength of 0.2 mol·dm-3. The ionic strength was maintained using sodium chloride and a phosphate buffer. The stability constants of the complex and the resulting Gibbs energy changes are obtained. The results are discussed in terms of the effect of solvent on protonation and complexation. © Springer Science+Business Media, LLC 2007  

The mechanism of electrochemical behavior of catechol in the presence of thiaproline is investigated by cyclic voltammetry, controlled-potential coulometry and spectrophotometric tracing of the reaction coordinate. The results indicate that thiaproline participate in with an ECEC mechanism in a nucleophilic (Michael) addition to o-quinone. Effect of pH of buffer solution on reaction pathway is studied and showed that addition of thiaproline to the o-quinone is performed only in solutions with pHs higher than 5. These results indicate that the addition of thiaproline is occurred first from amine functional group. In the second step, the addition of carboxylate group of thiaproline to C-5 of... 

Electrochemical oxidation of catechol in the presence of 3-mercapto-1,2,4-triazole (MTA) as a nucleophile in aqueous buffered solutions was studied by cyclic voltammetry and controlled-potential coulometry. The mechanism of electrochemical reaction is confirmed by spectrophotometric tracing in various times of controlled-potential coulometry. The voltammetric and spectrophotometric foundations indicate that a 1,4 Michael addition of MTA from its thiol moiety to the electrochemically derived o-quinone is occurred. The electrochemical synthesis of Michael addition product has been successfully accomplished by controlled-potential coulometry in a divided H-type cell and the reaction product was... 

A series of previously reported mononuclear Cu(II) and homodinuclear Cu(II)Cu(II) complexes, as well as, novel mononuclear Cu(II), homodinuclear Cu(II)Cu(II), and heterodinuclear Cu(II)Ni(II) complexes of a phenol-based dinucleating ligand with two different N(amine)2O2 and N(imine)2O2 coordination sites, were synthesized and characterized by elemental analyses, infrared and electronic absorption spectroscopies and conductivity measurements. The electrochemical behavior and catecholase-like activity of the complexes were also studied using cyclic voltammetry and UV-vis spectrophotometry, respectively. Our results show that the dinuclear complexes are more effective catalysts in the oxidation...