Search results for "DETECT"

2009

Abstract. Systematic laboratory experiments were performed to investigate quantification of various species with two versions of the Aerodyne Aerosol Mass Spectrometer, a Quadrupole Aerosol Mass Spectrometer (Q-AMS) and a compact Time-of-Flight Aerosol Mass Spectrometer (c-ToF-AMS). Here we present a new method to continuously determine the detection limits of the AMS analyzers during regular measurements, yielding detection limit (DL) information under various measurement conditions. Minimum detection limits range from 0.03 μg m−3 (nitrate, sulfate, and chloride) up to 0.5 μg m−3 (organics) for the Q-AMS. Those of the c-ToF-AMS are found between 0.003 μg m−3 (nitrate, sulfate) and 0.03 μg …

Improvement of the atomic fluorescence determination of mercury by using multicommutation

2002

Atomic fluorescence spectrometry (AFS) determination of Hg has been improved by exploiting the possibilities of the multicommutation approach in order to outline a fully mechanised system which supplies the same sensitivity as the use of continuous measurements, reducing drastically the reagents consumed and waste generation. The use of multicommutation with a simultaneous reduction of the liquid–gas separator volume and the insertion point modification of argon transport gas provides a sensitivity of the AFS measurements of 300 mV ng−1 ml (using a full scale of 1000 mV), a limit of detection (3 s) of 1.3 ng l−1 and relative standard deviation values below 0.1% for 10 independent measuremen…

Silver based sensors from CD for chloride ions detection

2021

This preliminary work shows a new and innovative way to produce silver based electrodes from compact discs and its application towards the detection of chloride ions. A complete sensor was obtained from the compact discs with working, reference and counter electrode made of silver. Chloride ions were detected by exploiting the high affinity of silver with this anion to produce silver chloride. This electrochemical oxidation of silver can be monitored by using an electrochemical technique such as linear scan voltammetry. Indeed, during linear scan voltammetry the oxidation of silver to silver chloride lead to a peak current that increases linearly with chloride concentration. Using this tech…

Bioanalysis of digoxin and its metabolites using direct serum injection combined with liquid chromatography and on-line immunochemical detection.

1994

Abstract An automated dual-column liquid chromatographic assay for digoxin is described. Serum samples are directly injected onto a restricted-access solid-phase extraction support. After liquid chromatographic (LC) separation on a C18 analytical column, antigenic analytes are detected by means of post-column immunochemical detection (ICD) using fluorescein-labelled antibodies against digoxigenin. The detection limit of this assay is 160 pg/ml (preconcentration of 1.0 ml serum). With the present method digoxin and three of its cross-reactive metabolites were determined in serum taken from patients which were orally administered a 1-mg dose of digoxin. The results obtained with LC—ICD were c…

Immunochromatographic Assay for Quantitation of Milk Progesterone.

1996

We describe a rapid immunochromatographic method for the quantitation of progesterone in bovine milk. The method is based on a 'competitive' assay format using the monoclonal antibody to progesterone and a progesterone-protein conjugate labelled with colloidal gold particles. The monoclonal antibody to progesterone is immobilized as a narrow detection zone on a porous membrane. The sample is mixed with colloidal gold particles coated with progesterone-protein conjugate, and the mixture is allowed to migrate past the detection zone. Migration is facilitated by capillary forces. The amount of labelled progesterone-protein conjugate bound to the detection zone, as detected by photometric scann…

The volatile inventory (F, Cl, Br, S, C) of magmatic apatite: An integrated analytical approach

2012

Abstract Apatite is ubiquitous in a wide range of magmatic rocks and its F–Cl–Br–S systematics can be used to decipher e.g., mixing processes within a magmatic complex and may give insights into fluid un-mixing and degassing processes during the emplacement and cooling of plutonic rocks. In this study, we analyzed a F-apatite (Durango, Mexico), a Cl-apatite (Odegarden, Norway) and apatites from five plutonic samples from the alkaline Mt. Saint Hilaire Complex (Canada) by means of Electron Microprobe Analysis (EPMA), Laser Ablation ICP-MS (LA-ICP-MS), Secondary Ion Mass Spectrometry (SIMS), pyrohydrolysis combined with ion chromatography, Fourier Transformed Infrared Spectroscopy (FTIR), Ins…

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…

Flow spectrophotometric determination of ammonium ion

1999

Abstract A flow procedure is proposed for the determination of ammonium ion. The sample in basic medium is forced through a solid-phase reactor containing immobilized AgCl on polymeric pearl beads. The released Ag + , complexed with the ammonia, gives a blue ternary complex with the aid of bromopyrogallol red and 1,10-phenanthroline which is spectrophotometrically monitored at 636 nm. The calibration graph is linear over the range 1–20 μg ml −1 ammonium ion, detection limit ( s / n  = 3)  0.35 μg ml −1 and relative standard deviation (slope) 1.9 % ( n  = 7). The sample throughput is 48 h −1 . The influence of foreign compounds is studied and the procedure is applied to ammonium ion determi…

Contribution to the adsorption voltammetric determination of manganese

1994

The adsorption voltammetric determination of Mn(II) with Bromopyrogallol Red (BPR) and Mordant Red 19 (MDR) has been investigated using a hanging drop mercury electrode. In NH3/NH4Cl solution, ligands and Mn(II) complexes give well separated voltammetric peaks after enrichment onto the electrode. The conditions for determining manganese by adsorption voltammetry with these reagents have been investigated in detail, as has the influence of foreign ions on the determination. The detection limits are 4·10−10 mol/L Mn for BPR and 8·10−10 mol/L Mn for MDR, respectively.

Urine polyamines determination using dansyl chloride derivatization in solid-phase extraction cartridges and HPLC

1999

The derivatization of biogenic amines such as putrescine, cadaverine, spermidine and spermine with dansyl chloride in solid phase extraction cartridges is described. Different types of filling materials were tested in order to have the highest retention of the different analytes. The best results were obtained by using C18 cartridges. The optimal conditions were: amine solution buffered at pH 12, 2 mM dansyl chloride (acetone-bicarbonate solution 20 mM (pH 9-9.5), 2 + 3 v/v) as reagent concentration, room temperature and 30 min reaction time. The developed procedure was applied to the determination of these polyamines in urine samples from healthy controls and cancer patients using HPLC wit…