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Tap Water Samples (tap + water_sample)

Distribution by Scientific Domains
Chemistry71%
Life Sciences28%

Selected Abstracts

Determination of Trace Amounts of Copper in Tap Water Samples with a Calix[4]arene Modified Carbon Paste Electrode by Differential Pulse Anodic Stripping Voltammetry

ELECTROANALYSIS, Issue 10 2007
Çelik Canpolat
Abstract A calix[4]arene modified carbon paste electrode was used for trace determination of copper. The study of the preconcentration of copper as well as the other heavy metal ions at the modified electrode, with subsequent measurement by differential pulse anodic stripping voltammetry (DPASV), indicates the efficient open-circuit accumulation of the analytes onto the electrode. Many parameters such as the composition of the paste, pH, preconcentration time and stirring rate influence the response of the measurement. The procedure was optimized for copper determination. For a 10-minute preconcentration time at pH,6.5,7.5, the detection limit (LOD) was 1.1,,g L,1. The optimized method was successfully applied to the determination of copper in tap water sample by means of standard addition procedure. The copper content of the sample was comparable with the result obtained with AAS method. [source]

Simultaneous Determination of Trace Zinc(II) and Cadmium(II) by Differential Pulse Anodic Stripping Voltammetry Using a MWCNTs,NaDBS Modified Stannum Film Electrode

ELECTROANALYSIS, Issue 23 2009
Qing Tian
Abstract A multiwalled carbon nanotubes,sodium dodecyl benzene sulfonate (MWCNTs,NaDBS) modified stannum film electrode was employed for the determination of cadmium(II) and zinc(II). The Sn/MWCNTs-NaDBS film electrode was prepared by applying MWCNTs,NaDBS suspension to the surface of the GCE, while the Sn film was plated in situ simultaneously with the target metal ions. Under optimal conditions, linear calibration curves were obtained in a range of 5.0 ,100.0,,g L,1 with detection limits of 0.9,,g L,1 for zinc(II) and 0.8,,g L,1 for cadmium(II), respectively. This film electrode was successfully applied to the determination of Zn(II) and Cd(II) in tap water sample. [source]

Determination of Trace Amounts of Copper in Tap Water Samples with a Calix[4]arene Modified Carbon Paste Electrode by Differential Pulse Anodic Stripping Voltammetry

ELECTROANALYSIS, Issue 10 2007
Çelik Canpolat
Abstract A calix[4]arene modified carbon paste electrode was used for trace determination of copper. The study of the preconcentration of copper as well as the other heavy metal ions at the modified electrode, with subsequent measurement by differential pulse anodic stripping voltammetry (DPASV), indicates the efficient open-circuit accumulation of the analytes onto the electrode. Many parameters such as the composition of the paste, pH, preconcentration time and stirring rate influence the response of the measurement. The procedure was optimized for copper determination. For a 10-minute preconcentration time at pH,6.5,7.5, the detection limit (LOD) was 1.1,,g L,1. The optimized method was successfully applied to the determination of copper in tap water sample by means of standard addition procedure. The copper content of the sample was comparable with the result obtained with AAS method. [source]

Adsorptive Stripping Voltammetric Determination of Amitrole at a Multi-Wall Carbon Nanotubes Paste Electdrode

ELECTROANALYSIS, Issue 5-6 2005
M. Chicharro
Abstract This work reports the excellent electrocatalytic activity of carbon nanotubes paste electrodes (CNTPE) prepared by dispersion of multi-wall carbon nanotubes (MWNT) within mineral oil toward the oxidation of 3-amino-1H -1,2,4-triazole (amitrole). The quantification is performed by adsorptive stripping voltammetry (AdSV). The influence of the paste composition and surface pretreatments as well as the amitrole accumulation conditions on the adsorption and further electrooxidation of this herbicide is described. After potentiodynamic pretreatment in 0.050,M phosphate buffer pH,7.4 the amitrole oxidation signal shifts 250,mV toward more negative potential and the sensitivity increases 29 fold, demonstrating that pretreated CNTPEs are extremely useful for a highly sensitive determination of amitrole down to the sub-,M levels. The oxidation peak current is proportional to the amitrole concentration over the range from 0.8 to 7.0,,M (5,min accumulation), with a detection limit of 0.6,,M (48,,gL,1) and a precision of 4.3%, n=20. The proposed method was used for the determination of amitrole in spiked river water (Alberche River (Madrid, Spain)) and tap water samples (Madrid, Spain) at levels higher than 0.6,,M. [source]

Indirect laser-induced fluorescence detection for capillary electrophoresis using a frequency-doubled diode laser

ELECTROPHORESIS, Issue 3 2003
Natalia Ragozina
Abstract A blue (452 nm) frequency-doubled diode laser with a quasi-cw optical output power of 10 ,W is used for indirect laser-induced fluorescence detection in combination with the capillary electrophoretic separation of inorganic anions. As fluorescing probe ion the anion of 8-hydroxypyrene-1,3,6-trisulfonic acid (HPTS) was selected having an absorption maximum of 454 nm in alkaline medium. Employing a capillary coated with linear acrylamide, baseline separation of eight inorganic anions was possible within 5 min. With a separation buffer containing 50 ,mol·L -1 HPTS and 10 mmol·L -1 lysine the limits of detection for sulfate, nitrite, nitrate, azide, thiocyanate, and chlorate were between 0.9 and 4.7 ,mol·L -1. Separation of chloride and sulfate was achieved by adding 0.25 mmol·L -1 calcium hydroxide to the separation buffer. Inorganic anions in several mineral and tap water samples have been determined with the technique developed and results are compared to data obtained by ion chromatography in combination with conductivity detection after conductivity suppression. [source]

Cytotoxic Bacillus spp. belonging to the B. cereus and B. subtilis groups in Norwegian surface waters

JOURNAL OF APPLIED MICROBIOLOGY, Issue 5 2004
Ø. Østensvik
Abstract Aims:, To investigate the presence and numbers of Bacillus spp. spores in surface waters and examine isolates belonging to the B. cereus and B. subtilis groups for cytotoxicity, and to discuss the presence of cytotoxic Bacillus spp. in surface water as hazard identification in a risk assessment approach in the food industry. Methods and Results:, Samples from eight different rivers with variable degree of faecal pollution, and two drinking water sources, were heat shocked and examined for the presence of Bacillus spp. spores using membrane filtration followed by cultivation on bovine blood agar plates. Bacillus spp. was present in all samples. The numbers varied from 15 to 1400 CFU 100 ml,1. Pure cultures of 86 Bacillus spp. isolates representing all sampling sites were characterized using colony morphology, atmospheric requirements, spore and sporangium morphology, and API 50 CHB and API 20E. Bacillus spp. representing the B. cereus and B. subtilis groups were isolated from all samples. Twenty-one isolates belonging to the B. cereus and B. subtilis groups, representing eight samples, were screened for cytotoxicity. Nine strains of B. cereus and five strains belonging to the B. subtilis group were cytotoxic. Conclusions:, The presence of cytotoxic Bacillus spp. in surface water represents a possible source for food contamination. Filtration and chlorination of surface water, the most common drinking water treatment in Norway, do not remove Bacillus spores efficiently. This was confirmed by isolation of spores from tap water samples. Significance and Impact of the Study:, Contamination of food with water containing low numbers of Bacillus spores implies a risk for bacterial growth in foods. Consequently, high numbers of Bacillus spp. may occur after growth in some products. High numbers of cytotoxic Bacillus spp. in foods may represent a risk for food poisoning. [source]

High-performance liquid chromatography determination of nitrated polycyclic aromatic hydrocarbons by indirect fluorescence detection

BIOMEDICAL CHROMATOGRAPHY, Issue 2 2009
Salma M. Al-Kindy
Abstract A high-performance liquid chromatography (HPLC) method for the analysis of nitrated polcyclic aromatic hydrocarbons (NPAHs) is reported. NPAH mixtures were pre-concentrated using solid-phase extraction and well resolved on a C18 column. They were detected using an indirect method involving the quenching of the emission from the fluorophores 5,6,7,8-tetrahydronaphthol (5,6,7,8-THN-1-OH), 7-amino-4-methyl coumarin (Coumarin 120, COU-120) and 3-hydroxy-4-(2-hydroxy-4-sulfo-1-naphthylazo)2-naphthalene carboxylic acid (Calcon carboxylic acid, CCA). Linear calibration curves were obtained in the range 1.1 × 10,9 to 1.1 × 10,8 mol/L. Using COU 120 as the fluorophore, the detection limit was 2.9 × 10,10 mol/L for 1-nitronaphthalene and 2.1 × 10,11 mol/L for 2-nitrofluorene. Recoveries of NPAHs from spiked tap water samples were between 88 and 100%. Copyright © 2008 John Wiley & Sons, Ltd. [source]