0000000000246877
AUTHOR
F. Blasco-gómez
Standard addition method in FIA. Comparison between different assemblies
A comparison between the different proposed methods to perform the standard addition in an on-line way (flow injection analysis) is made. The different assemblies (reverse and conventional FIA) and the employed standards in every method are compared. Three analyses were carried out, two of them were analyses of samples of pH indicators (methylorange and chlorophenol red) prepared at an acid pH, while the standards were prepared at a basic pH. The third analysis was the analysis of chloride in different synthetic waters with a perfectly known composition for all the ions present in the samples. Besides a new method to perform the on-line standard addition is proposed, trying to reduce the co…
H-Point Curve Isolation Method for Coupled Liquid Chromatography and UV−Visible Spectrophotometry
The H-point curve isolation method (HPCIM) for the detection of unknown interferences in chromatography is proposed. The method allows one to estimate the UV-vis spectra of interfering species in a sample as well as to test the purity of the chromatographic peaks. Besides the detection of the unknown interferences in a sample, this method allows one to calculate the concentration of an analyte in the presence of unknown compounds. To illustrate the reliability of the proposed method, samples of diuretics and amphetamines have been analyzed by normal- and reversed-phase high-performance chromatography.
The generalized H-point standard-additions method to determine analytes present in two different chemical forms in unknown matrix samples. Part II. Cr(vi) determination in water samples by absorption spectrophotometry
The generalized H-point standard-additions method (GHPSAM) is used in order to obtain the total Cr(VI) and chromate concentration in water samples whose matrices are completely unknown. Moreover, a new methodology, which is a modification of the GHPSAM, is proposed for the simultaneous determination of the two major chemical forms of Cr(VI) present in the sample. The method is based on the location of spectral intervals where the behaviour of the interferent absorbance can be considered as linear. From these intervals, the analyte concentration free from bias error can be estimated. Spiked samples of dig and harbour water measured in the UV–visible spectral region have been tested to check …
Principal component analysis for the selection of variables in the application of the H-point and generalised H-point standard addition method
The present paper deals with the selection of variables for the H-point and generalised H-point standard additions methods (HPSAM and GHPSAM, respectively). Both methods are applied for the resolution of spectroscopic interfered signals in the UV-vis range. The HPSAM is a suitable method for the resolution of binary and ternary mixtures when the interferent is known. The GHPSAM is applied for the resolution of samples that contain unknown interferents. In this paper, a method based on the study of a principal components analysis (PCA) for the selection of variables for the HPSAM and GHPSAM is proposed. The PCA results show the isolation of the analyte signal from the sample signal, achieved…
The generalized H-point standard-additions method to determine analytes present in two different chemical forms in unknown matrix samples. Part I. General considerations
This paper shows how the generalized H-point standard-additions method (GHPSAM) can be used to obtain the total concentration or concentrations of different chemical forms of an analyte when the matrix of the sample is completely unknown. The spectral regions where the interferent behaviour can be considered as linear are found and the analyte concentration free from bias error is estimated. This paper includes the already published features of the GHPSAM and a new modification of this method which allows the simultaneous determination of two chemical forms of an analyte in a sample.
Curve resolution procedure for isolating the spectra of unknown interferences from the sample spectrum in analyte determinations
The method described is based on the selection of a wavelength in the sample spectrum that is called ‘reference wavelength’, all measured wavelengths are previously assayed in order to select this reference wavelength. Several wavelengths can be used as the reference. The interferent spectrum is calculated as a function of the interferent absorbance at this wavelength, making use of the ratio between the absorbance of the analyte at the selected wavelength and at every measured wavelength. The proposed methodology can estimate the unknown interferent spectrum from the sample and pure analyte spectra. As a quality guarantee of the estimated spectrum, its shape is also estimated in spiked sam…