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101.
Hassan Ali Zamani Mohammad Reza Ganjali Masoud Salavati-Niasari 《Transition Metal Chemistry》2008,33(8):995-1001
A Fe3+ ion-selective membrane sensor was fabricated from polyvinyl chloride (PVC) matrix membrane containing bis-bidentate Schiff
base (BBS) as a neutral carrier, sodium tetraphenyl borate (NaTPB) as anionic excluder, and o-nitrophenyloctyl ether (NPOE) as a plasticizing solvent mediator. The effects of the membrane composition, pH, and additive
anionic influence on the response properties were investigated. The best performance was obtained with a membrane containing
32% PVC, 62.5% NPOE, 3% BBS, and 2.5% NaTPB. The electrode shows a Nernstian behavior (slope of 19.3 ± 0.6) over a very wide
iron ion concentration range (1.0 × 10−7–1.0 × 10−2 M) and has a low detection limit (7.4 × 10−8 M). The potentiometric response of the sensor is independent of pH of the solution in the pH range 1.9–5.1. The proposed
sensor has a very low response time (<15 s) and a good selectivity relative to a wide variety of other metal ions including
common alkali, alkaline earth, heavy, and transition metal ions. The electrode can be used for at least 60 days without any
considerable divergence in potentials. The proposed sensor was successfully applied as an indicator electrode for the potentiometric
titration of 1.0 × 10−2 M Fe3+ ions with a 1.0 × 10−4 M EDTA and the direct determination of Fe3+ in mineral water and wastewater samples. 相似文献
102.
Maryam Ebrahimi Jahan Bakhsh Raoof Reza Ojani 《Journal of the Iranian Chemical Society》2018,15(8):1871-1880
In the present paper, we used single-stranded poly-T (100% thymine bases) and poly-C (100% cytosine bases) nucleic acids as DNA probes for selective and sensitive individual electrochemical determination of Hg2+ and Ag+, respectively, on the multi-walled carbon nanotube paste electrodes (MWCNTPEs) using [Fe(CN)6]3?/4? as electroactive labels. In the presence of Hg2+ and Ag+, the probe–Hg2+/Ag+ interactions through T–Hg2+–T and C–Ag+–C complexes formation could cause the formation of a unimolecular hybridized probe. This structure of probe led to its partial depletion from electrode surface and facilitation of electron transfer between [Fe(CN)6]3?/4? redox couple and electrode surface, resulting in the enhanced differential pulse voltammetry (DPV) oxidation current of [Fe(CN)6]3?/4? at the probe-modified electrode surface. We applied the difference in the oxidation peak currents of [Fe(CN)6]3?/4? before and after Hg2+/Ag+–DNA probe bonding (?I) for electrochemical determination of these heavy metal ions. Detection limits were 8.0?×?10?12 M and 1.0?×?10?11 M for Hg2+ and Ag+ ions determination, respectively. The biosensors were utilized to determine the weight percent of toxic metals, i.e., silver and mercury in dental amalgam filling composition. The results of their practical applicability in analysis of the amalgam sample were satisfactory. 相似文献
103.
In this paper, molecular dynamics simulation was performed to investigate the liquid∕vapor interfacial structure of neat polar liquids. Large-scale ensembles of liquid pyridine and its alkyl derivatives, 4-methylpyridine and 4-ethylpyridine, were simulated by classical molecular dynamics at 298 K. For the liquid system of low polarity, the surface density profile of the atoms meet exactly at the middle of interfacial region, and atoms of hydrophobic nature can be hardly discriminated from hydrophilic ones in either vapor or liquid sides. For a liquid system of high polarity, the density profile of atoms with different nature is highly discriminated all over the interfacial region, and as the polarity increases, a dense region of atomic density is clearly developed in the subsurface region. The recognized bivariate method was also used to study the molecular orientational distribution quantitatively. Orientational analysis of the three liquid systems indicates that the pyridine ring plane in the outmost surface tends to be vertical. Its tendency in the innermost interfacial region is parallel. The orientational states available to 4-ethylpyridine and pyridine are discriminated by predicting the possibility of a bisector-wise tumbling for the ring plane in pyridine and a side-wise tumbling in 4-ethylpyridine. The orientational distribution maps explain the trend of experimental surface tension and surface entropy. As the dipole moment of these liquids increases with the alkyl chain length, the surface structural profile changes from a regular definite one to a surface of complex atomic structure involving a dense phase near the interface. The development of dense region in alkyl derivatives is the result of segregation of molecules due to the alkyl group, which is captured and discriminated by molecular dynamics simulation even when the length of a short alkyl chain is increased by one carbon atom. 相似文献
104.
In this paper multivariate response surface methodology (RSM) has been used for the optimization of hydrodistillation-headspace solvent microextraction (HD-HSME) of thymol and carvacrol in Thymus transcaspicus. Quantitative determination of compounds of interest was performed simultaneously using gas chromatography coupled with flame ionization detector (GC-FID). Parameters affecting the extraction efficiency were assessed and the optimized values were 5 min, 2 μL and 3 min for the extraction time, micro-drop volume and cooling time after extraction, respectively. The amounts of analyte extracted increased with plant weight. The calibration curves were linear in the ranges of 6.25-81.25 and 1.25-87.50 mg L−1 for thymol and carvacrol, respectively. Limit of detection (LOD) for thymol and carvacrol was 1.87 and 0.23 mg L−1, respectively. Within-day and between-day precisions for both analytes were calculated in three different concentrations and recoveries obtained were in the range of 89-101% and 95-116% for thymol and carvacrol, respectively. 相似文献
105.
BALALAIE Saeed CHADEGANI Fatemeh DARVICHE Fatemeh BIJANZADEH Harnid Reza 《中国化学》2009,27(10):1953-1956
A new and efficient method for the synthesis of 1,8‐dioxo‐9‐aryl‐decahydroacridine derivatives was developed via a one‐pot three component reaction of dimedone, aromatic aldehydes and ammonium acetate in the presence of ammonium chloride, or Zn(OAc)2·2H2O or L‐proline separately in water in the short period of time and high yields. 相似文献
106.
107.
Siavash Riahi Mohammad Reza Ganjali Maryam Hariri Shaghayegh Abdolahzadeh Parviz Norouzi 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2009,74(1):253-258
In this paper, a sensitive, easy, efficient, and suitable method for the calculation of Kf values of complexation between one derivative of Dansyl chloride [5-(dimethylamino) naphthalene-1-sulfonyl 4-phenylsemicarbazide] (DMNP) and Lanthanide(III) (Ln) ions is proposed, using both spectrofluorometric and spectrophotometric methods. Determination of Kf showed that DMNP was mostly selective towards the erbium (III) ion. The validity of the method was also confirmed calculating the Stern–Volmer fluorescence quenching constants (Ksv) that resulted in the same consequence, obtained by calculating the Kf of complexation values. In addition, the UV–vis spectroscopy was applied for the determination of Kf only for the Ln ions that had interactions with DMNP. Finally, the DFT studies were done on Er3+ and the DMNP complex for distinguishing the active sites and estimating the pair wise interaction energy. It can be concluded that this derivative of Dansyl chloride with inherent high fluorescence intensity is a suitable reagent for the selective determination of the Er3+ ion which can be used in constructing selective Er3+ sensors. 相似文献
108.
Thermal reduction has been applied to the preparation of copper nanoparticles (Cu-NPs) using three kinds of nonionic surfactants (Triton X-100, Tween-80, and dodecylamine). The Cu-NPs were formed by decomposition of copper(II) oxalate in presence of triphenylphosphine. The effect of the surfactants on the formation of the Cu-NPs was studied via X-ray diffraction, scanning electron microscopy, energy dispersive analysis of X-rays, transmission electron microscopy, thermogravimetric differential thermal analyses, and Fourier transform infra-red spectroscopy. It is shown that the Cu-NPs have an fcc crystal structure. Depending on the surfactant used, Cu-NPs with diameters between 8 and 20 nm can be prepared. The smallest Cu-NPs (8 nm) were formed in the presence of micelles of dodecylamine (yield 49%), while the largest particles (20 nm) were obtained with Triton X-100 (yield 99%). The use of Triton X-100 results in the highest yield and most uniform Cu-NPs. 相似文献
109.
110.