Search results for "Absorbance"
showing 10 items of 192 documents
Flow injection near-infrared determination of ethanol in chloroform
1995
A simple and direct flow injection (FIA) procedure has been developed for the determination of the stabilizing agent ethanol in chloroform samples. The procedure is based on the use of the absorbance band of ethanol in the near-infrared (NIR) region at 2272 nm, measured in front of a reference sample of chloroform stabilized with amylene. The method developed provides a limit of detection of 0.0045% (v/v) and a dynamic range until 10% (v/v) with a typical variation coefficient of 0.4% for six independent analysis of a real sample containing approximately 1% (v/v) of ethanol. The sample injection frequency allowed by the method is 78 h−1.
Comparative study of reflectance cells for PLS-FTIR determination of sugars in soft drinks
1998
A comparative study has been carried out between a horizontal Attenuated Total Reflectance (h-ATR) cell and a Cylindrical Internal Reflection (CIR) cell (CIRCLE cell). Both cells were employed for the determination of glucose, fructose, sucrose and total sugar in soft drinks and fruit juices using absorbance measurements at two resolution values (4 and 8 cm–1). Data were processed by Partial Least Squares regression (PLS). Using a resolution of 4 cm–1, mean relative errors of prediction from 0.6% to 1.3% were obtained using the horizontal-ATR and from 0.6% to 2.8% using the CIRCLE cell resulting in a limit of detection from 0.03% in the case of sucrose to 0.21% for total sugar for the h-ATR…
New optical paper sensor for in situ measurement of hydrogen sulphide in waters and atmospheres
2016
A novel and low-cost colorimetric sensor for the determination of hydrogen sulphide in environmental samples has been developed. This sensor is based on the immobilization of the reagent N,N-Dimethyl-p-phenylenediamine and FeCl3 in paper support, in which the H2S is adsorbed in order to give rise to the formation of methylene blue as reaction product. The sensor has been applied to determine H2S in water and air samples. Two different sampling systems for H2S caption from the air have been assayed: active and passive sampling. The analytical properties of the different systems have been obtained and compared. The analytical signals, corresponding to the methylene blue, have been obtained me…
Flow-injection determination of water in organic solvents by near-infrared spectrometry
1993
Abstract A flow-injection (FI) procedure was developed for the direct determination of water in organic solvents by using the O-H stretch absorbance band of water in the near-infrared (NIR) region. Dichloromethane was employed as a test solvent to study the influence of the flow parameters (carrier flow and sample injection volume) and time interval on the sensitivity and repeatability of the FI-NIR measurements. The developed procedure permits the determination of water in dichloromethane and isobutyl methyl ketone samples with limits of detection of 0.01 and 0.005% (v/v), respectively. Real and spiked samples of solvents were analysed by FI-NIR and accurate results were found. The method …
Determination of carbonates in waters by on-line vapor generation FTIR
1998
Abstract An electrically heated gas-permeation unit (GPU) has been employed for the vapor-generation Fourier transform infrared (FTIR) determination of total carbonate in waters. The developed method is based on the simultaneous injection of 100 μ l sample and 100 μ l nitric acid in a two-channel manifold with a merging zone, which provides the generation of CO 2 through the GPU, heated at 90°C, from which CO 2 is swept by a stream of N 2 to a long-path infrared gas cell. Absorbance measurements were made in the range from 2500 to 2150 cm −1 and the corresponding flow injection recordings were obtained as a function of time. The areas of these peaks are interpolated in a calibration equatio…
Fourier-transform infrared determination of nicotine in tobacco samples by transmittance measurements after leaching with CHCl3
1998
Abstract A new procedure is proposed for the FT-IR spectrometric determination of nicotine in tobacco. The method is based on the extraction of nicotine in CHCl 3 from tobacco samples, wetted with an aqueous solution of NH 3 (0.1 M), and the measurement of absorbance in the stopped-flow mode at 1316 cm −1 , using a spectral baseline correction established from 1334 to 1300 cm −1 . The procedure developed does not requires a complex sample preparation, and provides a limit of detection of 0.045 mg ml −1 nicotine, a sampling frequency of 3.3 h −1 and a coefficient of variation of 0.3% for five independent measurements of a tobacco sample with a nicotine content of 1.5% w/w. The accuracy of th…
Flow injection spectrophotometric determination of boron in ceramic materials.
1998
Abstract A flow injection spectrophotometric method for the determination of boron in ceramic materials is described. The method is based on spectrophotometric measurement of the decrease in the pH produced by the reaction between boric acid and mannitol in the presence of an acid-base indicator. A bichannel FI (flow injection) manifold in which the sample solutions were injected into deionized water (at pH 5.4) and the stream was later merged with the reagent stream (a mannitol solution containing 1×10 −4 mol l −1 bromocresol green at pH 5.4), was used. Transient signals were monitored at 616 nm. A theoretical model which describes the dependence between the absorbance values and boric aci…
Automated Fourier Transform near Infrared Determination of Buprofezin in Pesticide Formulations
2005
An automated procedure has been developed for Fourier transform near infrared (FT-NIR) determination of buprofezin in pesticide formulations. This methodology is based on on-line pesticide extraction with acetonitrile from solid samples and its determination by using peak area absorbance measurements between 2147 and 2132 nm, corrected with a horizontal baseline established at 2091 nm. The repeatability, as a relative standard deviation of five independent analyses of 18.9 mg g−1 of buprofezin, was 0.06% and the limit of detection 5 mg L−1. The reagent consumption was clearly reduced compared with a chromatographic reference procedure from 40.4 mL acetonitrile per sample, required by high …
Determination of aniline in vegetable oils by diazotization and coupling in a microemulsion medium
1990
Abstract A microemulsion containing sodium dodecyl sulphate and n -pentanol in a mass ratio of 1 : 4, water and a vegetable oil was investigated using pseudo-tenary phase diagrams. The medium can co-solve important amounts of vegetable oils and aqueous solutions over a wide range of ionic strengths. A procedure for the determination of 1.4–140 μg ml −1 of aniline in vegetable oils using ionic diazotization and coupling reactions was developed. The absorbance was measured in an optically clear microemulsion containing 4% or 20% of oil. The procedure is much simpler and rapid than the official chromatographic methods and gives almost the same limits of detection (ca. 05 μg ml −1 ) using no mo…
Spectrophotometric estimation of bicalutamide in tablets
2007
A simple, sensitive, rapid, accurate and precise spectrophotometric method has been developed for the estimation of bicalutamide in bulk and pharmaceutical dosage forms. Bicalutamide shows maximum absorbance at 272 nm with molar absorptivity of 2.3399×10(4) l/mol/cm. Beer's law was obeyed in the concentration range of 1.5-18 μg/ml. The limit of detection and limit of quantification were found to be 0.1 and 0.4 μg/ml, respectively. Results of analysis were validated statistically and by recovery studies.