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1.
Simultaneous determination of binary mixtures pyridoxine hydrochloride and thiamine hydrochloride in a vitamin combination using UV-visible spectrophotometry and classical least squares (CLS) and three newly developed genetic algorithm (GA) based multivariate calibration methods was demonstrated. The three genetic multivariate calibration methods are Genetic Classical Least Squares (GCLS), Genetic Inverse Least Squares (GILS) and Genetic Regression (GR). The sample data set contains the UV-visible spectra of 30 synthetic mixtures (8 to 40 microg/ml) of these vitamins and 10 tablets containing 250 mg from each vitamin. The spectra cover the range from 200 to 330 nm in 0.1 nm intervals. Several calibration models were built with the four methods for the two components. Overall, the standard error of calibration (SEC) and the standard error of prediction (SEP) for the synthetic data were in the range of <0.01 and 0.43 microg/ml for all the four methods. The SEP values for the tablets were in the range of 2.91 and 11.51 mg/tablets. A comparison of genetic algorithm selected wavelengths for each component using GR method was also included. 相似文献
2.
Nihan?Kaya Erdal?Karadurmus Ahmet?AlicilarEmail author 《Central European Journal of Chemistry》2005,3(3):511-519
An attempt was made to study the oxidation of manganese by air in synthetic waters. A series of batch experments were performed
at differnet values of concentration, temperature and pH. Unoxidized manganese in the solution was determined by formaldoxime
spectrometric method. Results of these studies indicated that the air oxidation of manganese soluble in water can be effectively
performed in basic media and that oxidation yield increasedwith an increase in pH and concentration. The yield was very high
in the presence of manganese dioxide, sepiolite or clinoptilolite in solution and, the oxidation was almost completed especially
at high values of pH and concentration. The reaction was found to be first order with respect to Mn2+ with a very low activation energy. A yield of 62% was obtained for the air oxidation of wastewater taken from the treatment
plant of Corum Municipality. 相似文献
3.
A new liquid chromatographic (LC)-chemometric approach was developed for the determination of sunset yellow (SUN) and tartrazine (TAR) in commercial preparations. This approach uses LC and chemometric calibration methods, i.e., classical least-squares (CLS), principal component regression (PCR), and partial-least squares (PLS), simultaneously. The combined LC-chemometric approaches, denoted as LC-CLS, LC-PCR, and LC-PLS, are based on photodiode array (PDA) detection at multiple wavelengths. Optimum chromatographic separation of SUN and TAR with allura red as the internal standard (IS) was obtained by using a Waters Symmetry C18 column, 5 microm, 4.6 x 250 mm, and 0.2 M acetate buffer (pH 5)-acetonitrile-methano-bidistilled water (55 + 20 + 15 + 10, v/v) as the mobile phase at a flow rate of 1.9 mL/min. The LC data sets consisting of the ratios of analyte peak areas to the IS peak area were obtained by using PDA detection at 5 wavelengths (465, 470, 475, 480, and 485 nm). LC-chemometric calibrations for SUN and TAR were separately constructed by using the relationship between the peak-area ratio and the training sets for each colorant. LC-chemometric approaches were tested for different synthetic mixtures containing SUN and TAR in the presence of the IS. These LC-chemometric calibrations were applied to a commercial preparation of the 2 colorants. The experimental results of the LC-chemometric approaches were compared with those obtained by a developed classical LC method using single-wavelength detection. 相似文献
4.
Continuous 1-dimensional wavelet transform (WT) was applied to the quantitative analysis of a vitamin combination of thiamine hydrochloride (THI) and pyridoxine hydrochloride (PYR) with strongly overlapping signals. Absorbance data from the UV-Vis absorption spectrum of width 1150 were subjected to Gauss1 and Gauss2 WTs. Because of its flexibility, data processing, and its high signal amplitude, the continuous WT method is a powerful tool for analysis of multicomponent mixtures. By measuring the amplitude signals corresponding to the selected zero-crossing points of the transformed signal, we obtained the calibration curve. The validation of the calibration graphs was confirmed with different mixtures of THI and PYR at various concentration ratios. A brief explanation of the continuous wavelet method is given. MATLAB 6.5 software was used to perform the calculations. The results of our study were compared with those obtained by spectroscopic, chemometric, and liquid chromatographic methods, and good agreement was found. 相似文献
5.
In this study, the new vic-dioxime ligand (LH2) and its complexes with CoII, NiII, CuII, ZnII, CdII and UO2VI are described. The structures of these complexes were characterized by elemental analyses, i.r., 1H- and 13C-n.m.r. spectra, u.v.–vis. spectroscopy, magnetic susceptibility measurements, conductivity measurements and thermogravimetric
analyses (t.g.a.). 相似文献
6.
Erdal Ertas Hakan Bildirir Onur Sahin Ipek Oksen 《Phosphorus, sulfur, and silicon and the related elements》2013,188(12):1835-1844
Abstract Syntheses of two analogues of tetrathiafulvalene (TTF), fused to 1,4-dithiin and thiophene rings, substituted with thiophene moieties, have been illustrated. The syntheses were accomplished through the reaction of a 1,8-diketone with phosphorus pentasulfide or Lawesson's reagent in boiling dry toluene. Conversion of the thioketones to their the oxo forms with mercury (II) acetate, was followed by self-coupling in freshly distilled boiling triethyl phosphite. Attempts for their electro-polymerizations through the thiophene groups at the peripherals were unsuccessful. Computational chemistry studies revealed that the thiophene groups did not exhibit enough spin densities to perform polymerization. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. 相似文献
7.
A novel chiral calix[4](azoxa)crown-7 (9) has been synthesized and its metal ion recognition properties investigated. The starting reagents, chiral diamine 5 and calix[4]arene diacid chloride derivative 8, were prepared according to literature methods. 1H and 13C NMR data show that 9 exists in a cone conformation. In liquid–liquid extraction experiments, 9 exhibits selectivity for Li+ among the other alkali metals and a good extraction ability for transition metal cations, suggesting its potential use in different fields, such as a sensor for ions as well as for chiral molecules. 相似文献
8.
Sonochemical synthesis and electrochemical characterization of α-nickel hydroxide: precursor effects
F. Sinem Ertaş Recep Kaş Uğur Ünal Özgür Birer 《Journal of Solid State Electrochemistry》2013,17(5):1455-1462
Sonochemical degradation of urea was employed to synthesize alpha-nickel hydroxide from different nickel salts. Utilization of ultrasound yielded products with properties significantly different than the products obtained by thermal degradation of urea. The effect of intercalating chloride, nitrate, acetate, and sulfate anions on morphology and electrochemical performance was studied. The sulfate-intercalated sample had the smallest interlayer spacing when obtained by the sonochemical method, contradicting all the previous thermal synthesis results. The specific capacitance trend also differed from the literature values, and the value for the sulfate-intercalated sample was larger than that of acetate- and nitrate-intercalated samples. Ultrasonic synthesis increased the specific capacitance of the sulfate-intercalated sample significantly. This sample was also the most reversible and had the highest charge efficiency. 相似文献
9.
Erdal Kendüzler 《International journal of environmental analytical chemistry》2013,93(11):843-853
A new and simple column-solid-phase extraction method has been developed to separate and preconcentrate trace cobalt in water and soil prior to its determination by flame atomic absorption spectrometry (FAAS). Different factors such as pH of sample solution, sample volume, amount of resin, flow rate of aqueous solution, volume and concentration of eluent, and matrix effects for preconcentration were optimized. Under optimized experimentally established conditions, an analytical detection limit of 0.44?µg?L?1, precision (RSD) of 1.9%, enrichment factor of 200, and capacity of resin of 82?mg?g?1 were obtained. The method was applied for cobalt determination by FAAS in tap water, natural drinking water, soil, and roadside dust samples. The accuracy of the method is confirmed by analysing standard reference material (Montana Soil, SRM 2711). 相似文献
10.
Simultaneous determination of seven phthalic acid esters in beverages using ultrasound and vortex‐assisted dispersive liquid–liquid microextraction followed by high‐performance liquid chromatography 下载免费PDF全文
Pelin Köseoğlu Yılmaz Abdulselam Ertaş Ufuk Kolak 《Journal of separation science》2014,37(16):2111-2117
A sensitive, rapid, and simple high‐performance liquid chromatography with UV detection method was developed for the simultaneous determination of seven phthalic acid esters (dimethyl phthalate, dipropyl phthalate, di‐n‐butyl phthalate, benzyl butyl phthalate, dicyclohexyl phthalate, di‐(2‐ethylhexyl) phthalate, and di‐n‐octyl phthalate) in several kinds of beverage samples. Ultrasound and vortex‐assisted dispersive liquid–liquid microextraction method was used. The separation was performed using an Intersil ODS‐3 column (C18, 250 × 4.6 mm, 5.0 μm) and a gradient elution with a mobile phase consisting of MeOH/ACN (50:50) and 0.2 M KH2PO4 buffer. Analytes were detected by a UV detector at 230 nm. The developed method was validated in terms of linearity, limit of detection, limit of quantification, repeatability, accuracy, and recovery. Calibration equations and correlation coefficients (> 0.99) were calculated by least squares method with weighting factor. The limit of detection and quantification were in the range of 0.019–0.208 and 0.072–0.483 μg/L. The repeatability and intermediate precision were determined in terms of relative standard deviation to be within 0.03–3.93 and 0.02–4.74%, respectively. The accuracy was found to be in the range of –14.55 to 15.57% in terms of relative error. Seventeen different beverage samples in plastic bottles were successfully analyzed, and ten of them were found to be contaminated by different phthalic acid esters. 相似文献