Search results for "Standard solution"
showing 9 items of 29 documents
Wine analysis: Study and comparison of techniques developed for the study of volatile constituents
1986
A number of headspace techniques have been compared, using a standard solution containing 12 compounds and a wine sample, viz.: (1) purge and cold trap injection; (2) dynamic headspace combined with liquidliquid extraction; (3) static headspace with and without preconcentration; (4) direct liquid injection. The sensitivity, reproducibility and speed of analysis were determined. Considering the results obtained and dependent on the purpose of the experiments and the number of samples to be examined the appropriate technique can be selected. ?? 1980 Friedr. Vieweg & Sohn Verlagsgesellschaft mbH.
Sensitive sequential-injection system for the determination of 2-phenylbenzimidazole-5-sulphonic acid in human urine samples using on-line solid-phas…
2003
Abstract 2-Phenylbenzimidazole-5-sulphonic acid (PBS) is an UV-filter contained in many cosmetics as a sunscreen. A direct, selective and sensitive method to determine traces of PBS is presented. The on-line separation of this compound from urine matrix was directly coupled with fluorimetric detection in a sequential-injection system. The separation was performed using a SAX microcolumn in which the analyte was retained and eluted selectively. The determination is carried out without any derivatization reaction, by directly measuring the intrinsic fluorescence of the analyte. The wavelengths of excitation and emission were 301 and 681 nm, respectively. On-line standard addition calibration …
Flow injection Fourier transform infrared determination of nicotine in tobacco
2000
A fully automated procedure is proposed for the Fourier transform infrared (FTIR) determination of nicotine in tobacco. The method is based on the on-line extraction of nicotine with CHCl3. Samples, weighed inside empty extraction cartridges, were humidified with NH3 and the cartridges were installed in a flow manifold in which they were extracted with 2 ml CHCl3 for 2 min, then 400 microliters of the extract were introduced into a micro-flow cell using a carrier of CHCl3 and the IR spectrum was registered continuously. The absorbance, in the wavenumber range 1334-1300 cm-1, was measured, obtaining a peak as a function of time. The area of this peak was interpolated on a calibration line es…
Comparison of Methods and Kits for Colorimetric Determination of Residual Chlorine in Water
1997
Abstract The use of 3,3',5,5'-tetramethylbenzidine (TMB) for residual chlorine determination in water offers 2 possibilities, one at pH 1-2 and absorbance measurement at 450 nm and another at pH 3.8-5.8 and measurement at 650 nm. The reaction of chlorine with TMB reaches its maximum sensitivity at pH 1-2. The detection limit is 2 ng/mL. A calibrated scale for colorimetric determination of residual chlorine in water with 3,3',5,5'-tetramethylbenzidine (TMB), prepared with tropaeolin O (C.I. 14270), is described. This scale is stable for several months and can be useful in replacing the conventional and much less stable scale prepared from standard solutions of oxochlorate (I). Kits for deter…
Quality control Fourier transform infrared determination of diazepam in pharmaceuticals
2007
A quality control procedure has been developed for the determination of diazepam in pharmaceuticals using Fourier transform infrared (FTIR) spectroscopy. The method involves the off-line extraction of diazepam with chloroform by sonication and direct determination in the extracts through peak area measurement in the interval between 1672 and 1682 cm(-1) using a baseline correction defined between 1850 and 1524 cm(-1). For standardization it was used an external calibration line established from standard solutions of diazepam in chloroform. The method provides a limit of detection of 0.04 mg per tablet (n=5), a relative standard deviation (R.S.D.) of 0.5% for 5 independent measurements of a …
Determination of ammonia and primary amine compounds and Kjeldahl nitrogen in water samples with a modified Roth's fluorimetric method.
2005
Abstract A method for the simultaneous determination of primary amino groups and ammonium ion has been proposed. The method is based in solution derivatization with o-Phthaldialdehyde/N-acetyl-cisteine (OPA/NAC) and fluorescence measurement of the formed isoindols. Analytical characteristics and description of the developed procedure have been provided. The calibration graphs for ammonium (up to 1.44 mg L−1 of N) and methylamine as primary amino model compound (up to 0.282 mg L−1 of N), were obtained. Bivariate and multivariate calibration models have been tested. The limits of detection were 0.07 mg L−1 of N and 0.004 mg L−1 of N for ammonium and amine, respectively. The procedure was firs…
Towards minimization of chlorinated solvents consume in Fourier transform infrared spectroscopy determination of Propamocarb in pesticide formulation…
2008
Abstract A method has been developed for Fourier transform infrared (FTIR) spectroscopy determination of Propamocarb in emulsifiable pesticide concentrate formulations. Five microliter sample was directly injected without any pretreatment in a CHCl 3 stream at 2 mL min −1 into a closed system and the FTIR spectra of sample and standard solutions were obtained using a nominal resolution of 4 cm −1 from 4000 to 900 cm −1 spectral region and accumulating 2 scans per spectrum. Propamocarb determination was based on the measurement of flow injection analysis (FIA) recording height established from FTIR peak area measurements from 1713 to 1703 cm −1 corrected using a baseline defined at 2000 cm −…
Analysis of archaeological samples and local clays using ICP-AES, TGâDTG and FTIR techniques
2000
Abstract The spectrochemical and thermal analysis of different archaeological samples as bricks, terra-cotta and local clays were carried out. The concentration of major and minor elements of samples was determined by sequential inductively coupled plasma atomic emission spectrometry. The method was tested by determining Si, Al, Fe, Ca, Mg, Mn, Pb, Cu, Zn, Ti, Na and K in the standard solutions and reference material GXR-4. The precision of the determination (relative standard deviation) ranged from 0.4 to 1.54%. The clay minerals are the main materials for the production of bricks and terra-cotta figures. Thermogravimetric (TG) and differential (TG–DTG) analysis and Fourier transform infra…
Determination of the four major surfactant classes in cleaning products by reversed-phase liquid chromatography using serially connected UV and evapo…
2016
Abstract A method for the simultaneous determination of the most frequently used surfactant families –linear alkyl benzenesulphonates (LAS), alkyl ether sulphates (AES), fatty alcohol ethoxylates (FAE) and oleins (soaps, fatty acid salts) – in cleaning products, has been developed. The common reversed phase octyl (C8), pentafluorophenyl and biphenyl columns were not capable of separating the anionic LAS and AES classes; however, since only LAS absorbs in the UV, these two classes were independently quantified using a C8 column and serially connected UV and ELSD detection. The best compromise to resolve the four surfactant classes and the oligomers within the classes was achieved with a C8 c…