In this paper,a new method for simultaneous spectrophotometric analysis of multi- component with double-system was developed.The multivariate calibration method,principal component analysis-partial least squares(PCA-P...In this paper,a new method for simultaneous spectrophotometric analysis of multi- component with double-system was developed.The multivariate calibration method,principal component analysis-partial least squares(PCA-PLS),was described and applied to the processing of measurement data.A demonstration,simultaneous determination of cobalt,nickel,copper,zinc and iron with double-system(5-Br-PADAP and PAR as chromogenic chelate reagents,respectively) was given.The results showed that the method with douhle-system gave better precision than those with single system and MLR(in this paper,AKC method was selected)did not give satis- fied precision in any situation.展开更多
A new simple spectrophotometric method was developed for the determination of binary mixtures without prior separation.The method is based on the generation of ratio spectra of compound X by using a standard spectrum ...A new simple spectrophotometric method was developed for the determination of binary mixtures without prior separation.The method is based on the generation of ratio spectra of compound X by using a standard spectrum of compound Y as a divisor.The peak to trough amplitudes between two selected wavelengths in the ratio spectra are proportional to concentration of X without interference from Y.The method was demonstrated by determination of two drug combinations.The first consists of the two antihyperlipidemics：atorvastatin calcium（ATV） and ezetimibe（EZE）,and the second comprises the antihypertensives：candesartan cilexetil（CAN） and hydrochlorothiazide（HCT）.For mixture 1,ATV was determined using 10 μg/mL EZE as the divisor to generate the ratio spectra,and the peak to trough amplitudes between 231 and 276 nm were plotted against ATV concentration.Similarly,by using 10 μg/mL ATV as divisor,the peak to trough amplitudes between 231 and 276 nm were found proportional to EZE concentration.Calibration curves were linear in the range 2.5-40 mg/mL for both drugs.For mixture 2,divisor concentration was 7.5 μg/mL for both drugs.CAN was determined using its peak to trough amplitudes at 251 and 277 nm,while HCT was estimated using the amplitudes between 251 and 276 nm.The measured amplitudes were linearly correlated to concentration in the ranges 2.5-50 and 1-30 μg/mL for CAN and HCT,respectively.The proposed spectrophotometric method was validated and successfully applied for the assay of both drug combinations in several laboratory-prepared mixtures and commercial tablets.展开更多
Two new sensitive spectrophotometric methods are reported for determination of tartrazine (Tz) (E102) in some commercial food samples. The first method involves two coupled reactions, the reduction of Cu(II) to Cu(I) ...Two new sensitive spectrophotometric methods are reported for determination of tartrazine (Tz) (E102) in some commercial food samples. The first method involves two coupled reactions, the reduction of Cu(II) to Cu(I) by the analyte in acetate buffer medium (pH = 5.9) at 30°C and the complexation reaction between Cu(I) and Tz oxidized form to yield Cu-Tz complex (method I). The other method is based on oxidation of Tz by alkaline KMnO4. These reactions are monitored spectrophotometrically at maximum absorbances 332 and 610 nm for methods (I and II) respectively. Variables affecting these reactions are carefully studied and the conditions are optimized. The stability constants are calculated at 293, 303, 313 and 323 K. The thermodynamic parameters, Gibb’s free energy change (ΔG), entropy change (ΔS), and enthalpy change (ΔH) associated with the complexation reaction are calculated and discussed. Under optimized conditions the proposed methods (I, II) obey Beer’s law 10.69 - 85.50, 5.34 - 34.12 μg·ml<sup>-1</sup> of Tz respectively. The molar absorptivity, sandel sensitivity, detection and quantification limits are calculated. Matrix effects are also investigated. The methods are successfully applied to the quantification of Tz in different commercially food samples. The results obtained are in good agreement with those obtained by the reported methods at the 95% confidence level.展开更多
Bipyridyl ruthenium dye N3 and N719 was synthesized, purified by the gel chromatogram method and characterized by the proton NMR and UV-Vis spectra. After the purification most of the impurities that decreased the pho...Bipyridyl ruthenium dye N3 and N719 was synthesized, purified by the gel chromatogram method and characterized by the proton NMR and UV-Vis spectra. After the purification most of the impurities that decreased the photoelectrochemical properties were removed and the open-circuit voltage （Voc）, short-circuit photocurrent density （Jsc） and overall photo-electric conversion efficiency （η） of the dye-sensitized solar cells （DSCs） increased dramatically. The standard curve of absorbance vs. concentration of N3 and N719 dye was achieved by using UV-Vis quantitative analytic spectrophotometry. This method was employed to determine the concentration of the dye solution after coating of TiO2 films. The linear concentration range of absorbance vs. concentration of N719 was between 6.25×10^-6 mol·L^-1 and 1×10^-4 mol·L^-1 with the molar extinction coefficient （ε） 1.58 ×10^4 L mol·L^-1·cm^-1 at a wavelength of 533 - 531 nm and 1.50 × 10^4 Lmol·L^-1·cm^-1 at a wavelength of 393 - 384 nm , accordingly. The linear concentration range of the N3 dye was 6.25 × 10^-6mol·L^-1 to 1.5× 10^-4 mol·L^-1 with ε of 1.47 × 10^4 L mol·L^-1· cm^-1 at a wavelength of 538 - 535 nm and 1.48 × 10^4 L ·mol·L^-1·cm^-1 at a wavelength of 399 - 393 nm.展开更多
基金This project was supported by the Natural Science Foundation of Jiangxi Province
文摘In this paper,a new method for simultaneous spectrophotometric analysis of multi- component with double-system was developed.The multivariate calibration method,principal component analysis-partial least squares(PCA-PLS),was described and applied to the processing of measurement data.A demonstration,simultaneous determination of cobalt,nickel,copper,zinc and iron with double-system(5-Br-PADAP and PAR as chromogenic chelate reagents,respectively) was given.The results showed that the method with douhle-system gave better precision than those with single system and MLR(in this paper,AKC method was selected)did not give satis- fied precision in any situation.
文摘A new simple spectrophotometric method was developed for the determination of binary mixtures without prior separation.The method is based on the generation of ratio spectra of compound X by using a standard spectrum of compound Y as a divisor.The peak to trough amplitudes between two selected wavelengths in the ratio spectra are proportional to concentration of X without interference from Y.The method was demonstrated by determination of two drug combinations.The first consists of the two antihyperlipidemics：atorvastatin calcium（ATV） and ezetimibe（EZE）,and the second comprises the antihypertensives：candesartan cilexetil（CAN） and hydrochlorothiazide（HCT）.For mixture 1,ATV was determined using 10 μg/mL EZE as the divisor to generate the ratio spectra,and the peak to trough amplitudes between 231 and 276 nm were plotted against ATV concentration.Similarly,by using 10 μg/mL ATV as divisor,the peak to trough amplitudes between 231 and 276 nm were found proportional to EZE concentration.Calibration curves were linear in the range 2.5-40 mg/mL for both drugs.For mixture 2,divisor concentration was 7.5 μg/mL for both drugs.CAN was determined using its peak to trough amplitudes at 251 and 277 nm,while HCT was estimated using the amplitudes between 251 and 276 nm.The measured amplitudes were linearly correlated to concentration in the ranges 2.5-50 and 1-30 μg/mL for CAN and HCT,respectively.The proposed spectrophotometric method was validated and successfully applied for the assay of both drug combinations in several laboratory-prepared mixtures and commercial tablets.
文摘Two new sensitive spectrophotometric methods are reported for determination of tartrazine (Tz) (E102) in some commercial food samples. The first method involves two coupled reactions, the reduction of Cu(II) to Cu(I) by the analyte in acetate buffer medium (pH = 5.9) at 30°C and the complexation reaction between Cu(I) and Tz oxidized form to yield Cu-Tz complex (method I). The other method is based on oxidation of Tz by alkaline KMnO4. These reactions are monitored spectrophotometrically at maximum absorbances 332 and 610 nm for methods (I and II) respectively. Variables affecting these reactions are carefully studied and the conditions are optimized. The stability constants are calculated at 293, 303, 313 and 323 K. The thermodynamic parameters, Gibb’s free energy change (ΔG), entropy change (ΔS), and enthalpy change (ΔH) associated with the complexation reaction are calculated and discussed. Under optimized conditions the proposed methods (I, II) obey Beer’s law 10.69 - 85.50, 5.34 - 34.12 μg·ml<sup>-1</sup> of Tz respectively. The molar absorptivity, sandel sensitivity, detection and quantification limits are calculated. Matrix effects are also investigated. The methods are successfully applied to the quantification of Tz in different commercially food samples. The results obtained are in good agreement with those obtained by the reported methods at the 95% confidence level.
基金supported by the National Basic Research Program of China (No. 2006CB202600)
文摘Bipyridyl ruthenium dye N3 and N719 was synthesized, purified by the gel chromatogram method and characterized by the proton NMR and UV-Vis spectra. After the purification most of the impurities that decreased the photoelectrochemical properties were removed and the open-circuit voltage （Voc）, short-circuit photocurrent density （Jsc） and overall photo-electric conversion efficiency （η） of the dye-sensitized solar cells （DSCs） increased dramatically. The standard curve of absorbance vs. concentration of N3 and N719 dye was achieved by using UV-Vis quantitative analytic spectrophotometry. This method was employed to determine the concentration of the dye solution after coating of TiO2 films. The linear concentration range of absorbance vs. concentration of N719 was between 6.25×10^-6 mol·L^-1 and 1×10^-4 mol·L^-1 with the molar extinction coefficient （ε） 1.58 ×10^4 L mol·L^-1·cm^-1 at a wavelength of 533 - 531 nm and 1.50 × 10^4 Lmol·L^-1·cm^-1 at a wavelength of 393 - 384 nm , accordingly. The linear concentration range of the N3 dye was 6.25 × 10^-6mol·L^-1 to 1.5× 10^-4 mol·L^-1 with ε of 1.47 × 10^4 L mol·L^-1· cm^-1 at a wavelength of 538 - 535 nm and 1.48 × 10^4 L ·mol·L^-1·cm^-1 at a wavelength of 399 - 393 nm.
