共查询到20条相似文献,搜索用时 31 毫秒
1.
Mónica Díaz-Pérez Manuel Aboal-Somoza Pilar Bermejo-Barrera Adela Bermejo-Barrera 《Central European Journal of Chemistry》2008,6(4):520-525
Preliminary results of development of a direct and fast method of determination of antimony in samples of tap water using
GFAAS are presented. The found levels of antimony were lower than permitted for human consumption. A mixture of Pd and Mg(NO3)2 (concentrations in the injected solution: 8.6 μg mL−1 and 5.8 μg mL−1 respectively) was used as the chemical modifier. The pyrolysis and atomization temperatures were 1000 and 1700°C, respectively
and the mean analytical recovery 98.2%.
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2.
The triplet excited state properties and photosensitization mechanisms of indigo were investigated based on density functional
theory calculations. The solvent effects on the photosensitization mechanisms of indigo have also been considered. The thermodynamic
feasibility of the possible 1O2 and O2·−-photogeneration pathways by triplet excited state indigo in different solvents was explored, in order to gain some deeper
insights into the photosensitization characters of the dye.
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3.
Dispersive liquid-liquid microextraction and liquid chromatographic determination of pentachlorophenol in water 总被引:1,自引:0,他引:1
Khalil Farhadi Mir A. Farajzadeh Amir A. Matin Paria Hashemi 《Central European Journal of Chemistry》2009,7(3):369-374
A simple and sensitive dispersive liquid-liquid microextraction method for extraction and preconcentration of pentachlorophenol
(PCP) in water samples is presented. After adjusting the sample pH to 3, extraction was performed in the presence of 1% W/V
sodium chloride by injecting 1 mL acetone as disperser solvent containing 15 μL tetrachloroethylene as extraction solvent.
The proposed DLLME method was followed by HPLC-DAD for determination of PCP. It has good linearity (0.994) with wide linear
dynamic range (0.1–1000 μg L−1) and low detection limit (0.03 μg L−1), which makes it suitable for determination of PCP in water samples.
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4.
Joanna Lenik Cecylia Wardak Barbara Marczewska 《Central European Journal of Chemistry》2008,6(4):513-519
Naproxen membrane electrodes based on different plasticizers and the quaternary ammonium salts (QASs) dimethyldidecylammonium
bromide, methyltrioctylammonium chloride, or tetraoctylammonium chloride, were prepared. The following basic parameters were
investigated for the optimal electrode: measurement range (10−4 − 10−1 mol L−1), slope of the linear range of the calibration curve (−58.3 mV decade−1), limit of detection (6.0 × 10−5 mol L−1), lifetime (2.5 months), dependence of the electrode potential on pH (5.5 − 9.0), reproducibility of potential (1.2 mV) and
selectivity coefficients in relation to selected organic and inorganic anions. The electrode was utilized for determination
of naproxen in tablets by the calibration curve method and the standard addition method.
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5.
Nitin A. Mirgane Sandip B. Kotwal Anil V. Karnik 《Central European Journal of Chemistry》2010,8(2):356-360
Ionic liquids (IL) are gaining importance as green solvents. Imidazolium ionic liquid [bmim]+[Cl]−, an environmentally benign solvent, was found to promote the Diels-Alder reaction between anthrone and maleimides at room
temperature with excellent yields. The ionic liquid played a dual role as solvent and catalyst.
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6.
Dmitriy A. Golovko Virender K. Sharma Olga. V. Pavlova Elena. A. Belyanovskaya Igor. D. Golovko Victoria. I. Suprunovich Radek Zboril 《Central European Journal of Chemistry》2011,9(5):808-812
A new amperometric titration method was developed for quantitative determination of ferrate(VI) (FeVIO4
2−) in the 7.06×10−5−5.73×10−3 M concentration range. Chromium(III) hydroxide solution was used as the titrant. The diffusion current (Id) had a linear
relationship with the concentration of ferrate(VI) and slopes were dependent on the concentration of NaOH. The amperometric
titration could detect a lower concentration of ferrate(VI) than could potentiometric and colorimetric titrations. The method
was applied successfully to determine concentrations of ferrate(VI), generated electrochemically, in strong alkaline solutions.
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7.
Mi?osz Mi?tkiewski Beata Powa?a Bartosz Staniszewski Maciej Kubicki W?odzimierz Urbaniak Cezary Pietraszuk 《Central European Journal of Chemistry》2011,9(4):728-736
Selected β-diketones bearing unsaturated derivatives have been demonstrated to undergo homo-metathesis and cross-metathesis with selected
olefins in the presence of Grubbs catalysts. The reactions led to respective homo- and cross-metathesis products mainly with
good yields and selectivities.
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8.
Zholt Kormosh Iryna Hunka Yaroslav Bazel Andriy Laganovsky Iryna Mazurenko Nataliya Kormosh 《Central European Journal of Chemistry》2007,5(3):813-823
The potentiometric response characteristics of a diclofenac selective electrode, based on ion association in different plasticizers,
were compared. The sensitivity, working range, detection limit and selectivity of membrane sensors demonstrated significant
dependence on the type of plasticizers. The potentiometric unit presented a linear response toward diclofenac concentrations
between 1 × 10−5 − 5 × 10−2 mol L−1, with slopes of approximately 60 mV dec−1, and exhibited a response time of 3 s. The potentiometric analysis of sodium diclofenac in pharmaceutical formulations was
perfomed by the membrane electrode proposed and compared with the results of potentiometric titration given by the Pharmacopoeia
of Ukraine.
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9.
Borjana V. Donkova Katja I. Milenova Dimitar R. Mehandjiev 《Central European Journal of Chemistry》2008,6(1):115-124
The precursors with a low manganese content ≤ 0.07% Mn were synthesized by spontaneous crystallization from Zn2+, Mn2+ and C2O4
2−-containing solutions. The initial ratio Zn2+:C2O4
2− = 1:1 and 1:2 influences the morphology and prevailing orientations of the crystallites in the oxalate samples. The presence
of such small Mn content in the samples does not change the morphology or size of the crystals. The ZnO and Mn/ZnO oxides
with manganese content from 0.51×10−2 to 15.1×10−2 Wt % are obtained after thermal decomposition of the oxalates. The oxides preserved the morphology of the precursors. The
catalytic tests show that the pure ZnO has a poor activity for CO oxidation reaction. Its doping with Mn promotes the catalytic
activity (up from twice to five times) in spite of the very low contents of the dopants. The observed increase of the activity
depends on both dopant concentration and Zn2+:C2O4
2− ratio, probably due to the different mechanism of the manganese inclusion and different morphology of the oxides. The catalysts
of the 1:2 series are more active in CO oxidation reaction.
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10.
Joanna Kurczewska Radosław Pankiewicz Grzegorz Schroeder 《Central European Journal of Chemistry》2012,10(5):1452-1458
Silica surface was modified with quaternary ammonium salts to give three matrices of different chain length. The synthesized supports were characterized by elemental analysis and infrared spectroscopy, as well as scanning electron microscopy and semi-empirical parametric method 5. Their exchange capacities for ClO4 −, F−, NO3 − and CH3COO− ions were investigated by conductometric titration. The amount of exchanged chloride ions from the matrix was studied for different initial anions concentration. The functionalized silica gel showed very good ability of perchlorate ions exchange from the water solution in room temperature. The anion-exchange properties were also studied in comparison to different number of reactive sites in the matrices. The increased number of chloride at the silica surface took effect on increased ability of ClO4 − anion exchange 相似文献
11.
Sylwia Smarzewska Sławomira Skrzypek Barbara Bachowska Piotr Bałczewski Witold Ciesielski 《Central European Journal of Chemistry》2011,9(5):840-845
Electrochemical oxidation of methylthiomethyleneisoquinolinium chloride (MTMIQ), the first alkylthiomethyl substituted ammonium
salt, which is fully miscible with water has been investigated by voltammetric (SWV) method using glassy carbon electrode.
On the electrode, MTMIQ undergoes oxidation at the potential near Ep = 0.07V (vs. Ag/AgCl/3 M KCl). The influence of the pH
of buffers, amplitude, frequency, step potential on the received signal was studied. The best results were obtained with a
citrate buffer at a pH of 5. The oxidation peak current used for MTMIQ voltammetric determination was in the range of 2–8×10−5 mol L−1, LOD = 3.7×10−6, LOQ = 1.2×10−5. The product of the oxidation was accumulated at the working electrode and was investigated by spectroscopic method. Mechanistic
pathways of the oxidation have been proposed.
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12.
Aleksandra Prichodko Kristina Jonusaite Vida Vickackaite 《Central European Journal of Chemistry》2009,7(3):285-290
A hollow fibre liquid phase microextraction for gas chromatographic determination of some p-hydroxybenzoic acid esters has
been developed. Chlorobenzene containing tetradecane as internal standard was used for the extraction. Optimized extraction
was carried out at room temperature for 40 min in the presence of 0.4 g mL−1 NaCl in the sample solution. Calibration was linear up to 30 mg L−1. Correlation coefficients were 0.996–0.998. Enrichment factors were 21, 95 and 154, and detection limits were 0.20, 0.03
and 0.01 μg mL−1 for methylparaben, ethylparaben and propylparaben, respectively. Reproducibility was acceptable with relative standard deviations
up to 11.7%. The technique was tested for water and urine analysis.
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13.
Ksenija R. Kumrić Tatjana M. Trtić-Petrović Ljubiša M. Ignjatović Jožef J. Čomor 《Central European Journal of Chemistry》2008,6(1):65-69
Lutetium has been determined by differential pulse anodic stripping voltammetry in an acidic solution containing Zn-EDTA.
Lutetium (III) ions liberated zinc (II), which was preconcentrated on a hanging mercury drop electrode and stripped anodically,
resulting in peak current linearly dependent on lutetium (III) concentration. Less than 0.4 ng mL−1 lutetium could be detected after a 2 min deposition.
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14.
Ibuprofen membrane electrodes based on different plasticizers: diisobutyl phthalate (DIBP), o-nitrophenyloctyl ether (o-NPOE),
dioctyl sebacate (DOS) and tetraoctylammonium 2-(4-isobutylphenyl)propionate were prepared. All electrodes show: a near Nernstian
slope of characteristic (58.3–60.9 mV decade−1) in the measurement range (10−4–10−1 mol L−1), limit of detection (5.0×10−5 mol L−1), really long lifetime (12 months), dependence of the electrode potential on pH (5.5–9.0), reproducibility of potential (0.6–1.2
mV) and selectivity coefficients in relation to some organic and inorganic anions. The electrodes were applied for the determination
of ibuprofen in tablets by the calibration curve method and the standard addition method.
相似文献
15.
Titania layers obtained by a sol-gel technique doped with redox mediator, Meldola’s Blue, were employed for construction of
a new NADH senor. Optimization of preparation process as well as experimental conditions affecting the response of the sensor
were examined. Under optimal conditions NADH could be determined in the wide linear range from 90 to 2300 μM with detection
limit 12 μM and a high sensitivity 12.5 nA μM−1. The usefulness of developed sensor was preliminarily checked in determination of NADH forming during enzymatic oxidation
of ethanol catalyzed by alcohol dehydrogenase (ADH).
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16.
The potential of modified multiwalled carbon nanotubes (a solid-phase extraction sorbent), for the simultaneous separation
and preconcentration of lead, cadmium and nickel; has been investigated. Lead, cadmium and nickel, were adsorbed quantitatively;
on modified multiwalled carbon nanotubes (in the pH range of 2–4). Parameters influencing, the simultaneous preconcentration
of Pb(II), Ni(II) and Cd(II) ions (such as pH of the sample, sample and eluent flow rate, type and volume of elution solution
and interfering ions), have been examined and optimized. Under the optimum experimental conditions, the detection limits of
this method. for Pb(II), Ni(II) and Cd(II) ions, were 0.32, 0.17 and 0.04 ng mL−1 in original solution, respectively. Seven replicate determinations, of a mixture of 2.0 μg mL−1 lead and nickel, and 1.0 μg mL−1 cadmium; gave a mean absorbance of 0.074, 0.151 and 0.310, with relative standard deviation 1.7%, 1.5% and 1.2%, respectively.
The method has been applied, to the determination of trace amounts of lead, cadmium and nickel; in biological and water samples,
with satisfactory results.
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17.
Chockalingam Karunakaran Premkumar Anilkumar 《Central European Journal of Chemistry》2009,7(3):519-523
Oxidation of iodide ion from an air-saturated solution under natural sunlight (900±50 W m−2) on the surfaces of TiO2, ZnO, Fe2O3, MoO3 and CeO2 enhances by 6 to 12-fold on application of a cathodic bias of −0.2 to −0.3 V (vs NHE) to the semiconductors; light, the semiconductor and dissolved oxygen are essential for iodine generation. The semiconductors
under an anodic bias of +0.2 to +0.3 V (vs NHE) fail to oxidize iodide ion from air-saturated solution under sunlight. Under cathodic bias, semiconductor mixtures like
TiO2-ZnO, TiO2-Fe2O3 and ZnO-Fe2O3 show enhanced photocatalytic activity, indicating improved charge separation in oxide mixtures. The mechanism of photocatalysis
under cathodic bias is discussed.
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18.
Abdülhadi Baykal Nermin Kasapoğlu Yüksel Köseoğlu Ali Cemil Başaran Hüseyin Kavas Muhammet S. Toprak 《Central European Journal of Chemistry》2008,6(1):125-130
A series of Ni-doped cobalt ferrites NixCo1−xFe2O4 (x = 0.0, 0.4, 0.6, 0.8, and 1.0) were prepared using microwave-induced combustion. Nickel, cobalt, and ferric nitrates were
used as starting materials and glycine as fuel. The influence of Ni content on the lattice parameter, stretching vibrations,
and magnetization was studied. XRD, FTIR, and SEM were used for structure, composition, and morphology investigation. A porous
network structure was observed with average particle size 60–67 nm. All samples had a cubic spinel structure. The unit cell
parameter “a” decreases linearly with nickel concentration due to the smaller ionic radius of nickel. Magnetization measurements
showed that coercivity decreased as Ni content increased; it increased with decreasing temperature.
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19.
Rafal Kruszynski 《Central European Journal of Chemistry》2008,6(4):542-548
2,4-dinitrophenylhydrazine hydrochloride hydrate (I) was determined by X-ray crystallography, and the intermolecular interaction
energies were calculated in terms of Natural Bond Orbital analysis. The asymmetric unit of (I) consists of a dinitrophenylhydrazinium
cation, a chloride anion and a water molecule. The interatomic distances and angles in (I) show no unusual values. In the
structure there are intermolecular N—H⊎⊎⊎O, N—H⊎⊎⊎Cl, O—H⊎⊎⊎Cl, C—H⊎⊎⊎O hydrogen bonds with bonding energy ranging form 16.03
to 0.76 kcal mol−1. These hydrogen bonds create the following N1 motifs: 6D, S(5), S(6), C(6), C(9). N1D motifs become infinite at the third level and are 2C32(6), C32(7).
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20.
Halil Turgut Şahin 《Central European Journal of Chemistry》2007,5(3):824-834
Attempts were made to plasma deposit an oriented π-conjugated polymer of pyrrole (Py) on paper surfaces in order to produce
electrically conductive layers. The N/C atomic ratio of 0.13–0.24 was observed for all treatment conditions. This implies
the nature of the deposition formed on the paper surface via pulsed plasma is different from that of pyrrole monomer. An increase
in conductivity of all pyrrole-plasma treated papers was observed. The 50 W RF-power with 5 min plasma exposed paper sample
shows 8.15 × 10−9 S·cm−1 conductivity. The conductivity measurements indicated a plasma-enhanced ring-opening reaction mechanism of pyrrole.
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