Search results for "Detection limit"
showing 10 items of 810 documents
Gaschromatographisch-massenspektrometrische identifizierung der durch umsetzung von aminen mit isocyanaten gebildeten harnstoffderivate
1977
Abstract Gas chromatographic-mass spectrometric identification of urea derivatives formed by the reaction of amines with isocyanates N,N′-Di- and N,N′,N′-trisubstituted ureas constitute suitable derivatives for the gas chromatographic (GC) determination of primary and secondary amines. The GC identification of N- tert. -butyl-,N′,N′-alkyl urea derivatives presented in the first communication has been succesfully confirmed by mass spectrometry (MS) and mass fragmentometry. The reproduced mass spectra of six N- tert. -butyl-,N′,N′-alkyl ureas were interpreted according to the decomposition mechanisms of less complicated alkyl ureas known from the literature. Using combined GC-MS the detection…
Indirect analysis of urea herbicides from environmental water using solid-phase microextraction.
2000
We described here a solid-phase microextraction procedure used to extract six urea pesticides-- chlorsulfuron, fluometuron, isoproturon, linuron, metobromuron and monuron--from environmental samples. Two polydimethylsiloxanes and a polyacrylate fiber (PA) are compared. The extraction time, pH control, addition of NaCl to the water and the influence of organic matter such as humic acid on extraction efficiency were examined to achieve a sensitive method. Determination was carried out by gas chromatography with nitrogen-phosphorus detection. The proposed method requires the extraction of 2 ml of sample (pH 4, 14.3%, w/v, NaCl) for 60 min with the PA fiber. The limits of detection range from 0…
Determination of the protein and free amino acid content in a sample using o-phthalaldehyde and N-acetyl-L-cysteine
1990
A spectrophotometric method is proposed for determining the protein content in a sample after total acid hydrolysis. In the procedure, free amino acids are caused to react with o-phthalaldehyde and N-acetyl-L-cysteine at pH 9.5, using isoleucine as the reference compound. Correction factors are used to take into account the differences between the molar absorptivities of the amino acid isoindoles and the recoveries of the amino acids after the hydrolysis treatment. The limit of detection was in the range 40-50 micrograms of protein, and the recoveries were usually 101 +/- 3% with a coefficient of variation lower than 4%. The free amino acid content in a partially hydrolysed protein was also…
Determination of heavy metal complexes with humic substances by HPLC/ICP-MS coupling using on-line isotope dilution technique
1997
An isotope dilution mass spectrometric (IDMS) method has been developed for the simultaneous determination of the complexes of 11 heavy metals (Ag, Cd, Cu, Mo, Ni, Pb, Tl, U, W, Zn and Zr) with humic substances (HS) by coupling HPLC with ICP-MS and applying the on-line isotope dilution technique. The HPLC separation was carried out with size exclusion chromatography. This HPLC/ICP-IDMS method was applied to samples from a brown water, ground water, sewage and seepage water as well as for a sample containing isolated fulvic acids. The total contents of heavy metals and of their complexes were analyzed in these samples with detection limits in the range of 5–110 ng/L. The analysis of heavy me…
Development of competitive enzyme-linked immunosorbent assays for boscalid determination in fruit juices
2012
Abstract Boscalid is a modern, broad-spectrum carboxamide pesticide highly efficient against most fungal diseases affecting valuable crops. In this study, a boscalid-mimicking derivative with a six-carbon spacer arm replacing the chlorine atom at the pyridine ring of the target molecule was synthesized and coupled to carrier proteins. Following rabbit immunization, antibodies against this agrochemical were obtained for the first time, and they were characterised in terms of affinity and specificity, tolerance to solvents, and robustness to changes in buffer pH and ionic strength, using two assay formats. Both of the optimised immunoassays showed limits of detection below 0.1 μg/L. Moreover,…
Enhanced spectrophotometric determination of nicotinic acid in a sodium dodecyl sulphate micellar medium.
1994
The spectrophotometric determination of pyridine and pyridine derivatives by means of the König reaction was studied in micellar media of sodium dodecyl sulphate (SDS), N-cetylpyridinium chloride and Triton X-100. The sensitivity was largely increased in SDS micellar medium. The attack of the pyridine ring with cyanogen bromide to produce a glutaconic aldehyde was not affected by the presence of SDS, but the yield of the coupling reaction with an arylamine to produce a polymethine dye was largely increased. In the SDS micellar medium, aniline was superior to other coupling reagents. The limits of detection (LODs) were 6 x 10(-7), 1 x 10(-6) and 5 x 10(-7)M for pyridine, pyrrol-ylmethylpyrid…
Allylated cyclodextrins as effective affinity materials in chemical sensing of volatile aromatic hydrocarbons using an optical planar Bragg grating s…
2013
We report on the application of perallyl-substituted α-, β- and γ-cyclodextrins to an optical planar Bragg grating refractive index sensor for the effective sensitization of the sensor for airborne volatile aromatic hydrocarbons. Thereby, the emphasis of this work lies on the comparison of the different cyclodextrin types regarding their suitability as affinity material assessed by the sensors sensitivity and response behavior. The opto-chemical sensor device showed an immediate and quick response to the application of the investigated analytes benzene, toluene and m-xylene as well as a linear dependence on the concentration of those analytes. Studies on the sensors sensitivity depending on…
Plasmonic optical sensors printed from Ag–PVA nanoinks
2014
In this paper we report on the use of a nanocomposite based on silver nanoparticles embedded in PVA as a plasmonic optical sensor to detect and quantify trace amounts of amines in gas and water, respectively. The transduction mechanism of the sensor is based on the changes of the LSPR band of Ag NPs when analyte molecules are chemisorbed on their surface. The Ag–PVA sensors are fabricated by means of a high-precision microplotter, a direct-write technology developed for printing materials from solution. The nanoink is formulated with a metal precursor (AgNO3) and a polymer (PVA) using an adequate mixture of solvents to meet the rheological requirements for the fluid dispensing process. The …
Modifying the reactivity of copper (II) by its encapsulation into polydimethylsiloxane: A selective sensor for ephedrine-like compounds
2018
This paper demonstrates that the reactivity of copper (II) can be modified through its entrappment in a polymeric matrix of polydimethylsiloxane (PDMS), which makes possible the reaction into the support instead of in solution. Amino-containing compounds such as amino acids, proteins and sugars, which react with Cu (II) in solution, do not react inside the polymer. As a prove of concept, a highly specific Cu (II) PDMS-based sensor for ephedrines has been developed in this work. When the sensors are put into contact with solutions of these drugs under basic conditions, a change in their color from pale green to purple is observed. This change enables the visual identification of ephedrine (E…
The PAH composition in limpets (Patella vulgate L.) from the coasts of Sicily (Italy)
2006
This article examines the presence, distribution, nature and sources of 19 Polycyclic Aromatic Hydrocarbons (PAH), in Patellae (patella vulgate L.) and seaweed (vulva) sampled in different stations of Sicilian coastal environments and analyzed for their polycyclic aromatic hydrocarbon (PAH) content. Analysis was performed by gas chromatography/mass spectrometry (GC/MS) with selected ion monitoring (SIM), after saponification of the sample and clean up of the extract. In the limpets the total concentration of polycyclic aromatic hydrocarbons ranged from 34 to 750 μg/Kg of dry matrix. The relative standard deviation (RSD) of the replicas on the concentrations of individual compounds ranged fr…