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  • 1
    ISSN: 0935-6304
    Keywords: Capillary GC ; Continuous liquid-liquid extraction ; Environmental applications ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The applicability of a liquid-liquid extraction system which is coupled on-line with a capillary gas chromatograph was studied for environmental and ecotoxicological analyses. The optimized and automated system was used for the determination of apolar and rather non-volatile organic compounds in aqueous samples. Relevant aspects of sample introduction, phase separation and selection of extraction solvent are discussed. Three routine-tipe applications are described, viz. an improved method for the determination of hexachlorocyclohexanes in ground water and the determination of the so-called NCC-ether and ACC-ether in ecotoxicological studies. Depending on the application studied, the concentration levels varied from 0.1 to 6000 μg/I, using ECD and/or FID detection. Typical coefficients of variation obtained with the total extraction-GC procedure were 2-25%.The system was found to be rugged, it saves time compared with set-ups involving off-line liquid-liquid extraction and considerably reduces the manual work load.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1040-7685
    Keywords: capillary GC ; reversed-phase LC ; on-line coupling ; solvent vapor exit ; pressure-balanced carrier gas system ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A large-volume introduction system for capillary gas chromatography (GC) is described which can be coupled on-line with reversed-phase liquid chromatography (LC) using 2 mm i.d. LC columns. An on-column interface with a special retention gap, coated with a very thin film (0.02 μm) of Carbowax was used. Insertion of a solvent vapor exit before the analytical gas chromatography column allowed the solvent evaporation rate for an azeotropic acetonitrile/water mixture (84:16, v/v) to increase from 20 to 175 μL min-1 at 91°C and 150 kPa inlet pressure. A volume of 200 μL of this mixture containing phenanthrene and the potential basic drug eltoprazine, could be injected into the retention gap at introduction rates up to 200 μL min-1, under partially concurrent solvent evaporation conditions. Repeatability (CV = 2.4%) and linearity (at least 10-1000 ng mL-1) were satisfactory. The Carbowax-coated retention gap has a relatively large retention power for the polar solute. This means that the solvent can be completely evaporated through the vapor exit without loss of analyte. With apolar solutes, losses will occur if evaporation is unduly prolonged. In order to allow the use of a nitrogen-phosphorus detector, a special pressure-balanced carrier gas circuit was designed and tested for total solvent-free performance of the detector. With this set-up, 150 μL injections of eltoprazine in the acetonitrile/water azeotrope were made at an introduction rate of 200 μL min-1. No traces of acetonitrile were detected, while analyte detectability was 20-fold higher than with the FID.Finally, the practicability of reversed-phase LC-GC was demonstrated by on-line heart-cutting of the phenanthrene-containing fraction from a 2 mm i.d. LC column using acetonitrile/water (84:16, v/v) as eluent, and analyzing it by capillary GC-FID.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0935-6304
    Keywords: Capillary GC ; On-line extractive alkylation ; On-line acylation ; Carboxylic acids ; Amines ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Gas chromatographic procedures are described for the determination of carboxylic acids and chlorinated anilines in water samples.Propionic acid and 2,6-difluorobenzoic acid in aqueous solution have been simultaneously alkylated and extracted by means of a continuous two-phase reaction system, and then quantitated by on-line coupled capillary gas chromatography; tetrahexyl-ammonium hydrogen sulfate was used as phase transfer catalyst and pentafluorobenzyl bromide as reagent.A factorial design approach was used to optimize on-line derivatization of aqueous propionic acid with regard to pH and concentration of phase transfer catalyst. Alkylation and extraction, under optimized conditions, followed by quantitation of the pentafluorobenzyl ester by flame ionization detection furnished a linear calibration for concentrations between 0.1 and 10 μg/ml. The relative standard deviation was 9-15 %.The continuous two-phase reaction system was also used to determine (chlorinated) anilines present in water at concentrations of 0.1-1 μg/ml; pentafluorobenzoyl chloride was used as reagent and analysis was performed by capillary gas chromatography with flame ionization or electron capture detection. The on-line acylation of p-chloroaniline was optimized with regard to pH, reagent concentration, and reaction time.The on-line reaction system worked satisfactorily for both applications, although excess reagent caused some problems with the chromatography.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0935-6304
    Keywords: On-line extraction ; Large volume introduction ; Capillary gas chromatography ; Atomic emission detection ; Solvent venting ; Pesticides ; Ground water ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The on-line coupling of a liquid-liquid extraction system with capillary gas chromatography using atomic emission detection (GC-AED) has been studied. The required large volumes of about 100 μl of an iso-octane solution can be introduced into the GC-AED system by using the AED solvent vent and a solvent vapor exit in front of the capillary analytical column. Test solutions containing several pesticides were detected using the carbon, chlorine, nitrogen and sulfur channels. Analyte detectability (in concentration units) was improved significantly and low concentractions of the test compounds could be determined (1-5 ng/ml). Aqueous samples were on-line extracted and analyzed. The precision of the large-volume injection itself as well as the total extraction-GC-AED system was satisfactory (RSD of ca. 2 and 4%, respectively). As a real-life application, several ground water samples were screened.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
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    PANGAEA
    In:  Supplement to: Egger, Matthias; Lenstra, Wytze K; Jong, Dirk; Meysman, Filip J R; Sapart, Célia-Julia; van der Veen, Carina; Röckmann, Thomas; Gonzales, S; Slomp, Caroline P (2015): Rapid sediment accumulation results in high methane effluxes from coastal sediments. PLoS ONE, 11(8), e0161609, https://doi.org/10.1371/journal.pone.0161609
    Publication Date: 2023-01-13
    Description: Will be submitted by the author
    Keywords: GCUWI; Gravity corer, UWITEC; Grevelingen Lake, Netherlands; Scharendijke_Site
    Type: Dataset
    Format: application/zip, 3 datasets
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  • 6
    Publication Date: 2023-02-07
    Keywords: DATE/TIME; DEPTH, sediment/rock; GCUWI; Gravity corer, UWITEC; Grevelingen Lake, Netherlands; Porosity; Scharendijke_Site
    Type: Dataset
    Format: text/tab-separated-values, 29 data points
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  • 7
    Publication Date: 2023-02-07
    Keywords: Acid volatile sulfides; Chromium reducible sulfides; DATE/TIME; DEPTH, sediment/rock; GCUWI; Gravity corer, UWITEC; Grevelingen Lake, Netherlands; Iron; Iron, total; Iron oxides; Molybdenum; Sample comment; Scharendijke_Site; Sulfur, total; Thorium-232
    Type: Dataset
    Format: text/tab-separated-values, 1364 data points
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  • 8
    Publication Date: 2023-02-12
    Keywords: Ammonium; DATE/TIME; DEPTH, sediment/rock; GCUWI; Gravity corer, UWITEC; Grevelingen Lake, Netherlands; Hydrogen sulfide; Iron 2+; Methane; Sample comment; Scharendijke_Site; Sulfate; Sulfate reduction rate; δ13C, methane; δ13C, methane, standard deviation; δ Deuterium, methane; δ Deuterium, methane, standard deviation
    Type: Dataset
    Format: text/tab-separated-values, 1054 data points
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  • 9
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    PANGAEA
    In:  Supplement to: Korte, Laura F; Brummer, Geert-Jan A; van der Does, Michèlle; Guerreiro, Catarina V; Hennekam, Rick; van Hateren, Johannes Albert; Jong, Dirk; Munday, Chris I; Schouten, Stefan; Stuut, Jan-Berend W (2017): Downward particle fluxes of biogenic matter and Saharan dust across the equatorial North Atlantic. Atmospheric Chemistry and Physics, 17(9), 6023-6040, https://doi.org/10.5194/acp-17-6023-2017
    Publication Date: 2023-09-11
    Description: Massive amounts of Saharan dust are blown from the African coast of North Africa across the Atlantic Ocean towards the Americas each year. This dust has, depending on its chemistry, direct and indirect effects on global climate including reflection and absorption of solar radiation as well as transport and deposition of nutrients and metals fertilizing both ocean and land. To determine the temporal and spatial variability of Saharan dust transport and deposition and their marine environmental effects across the equatorial North Atlantic Ocean, we have set up a monitoring experiment using deep-ocean sediment traps as well as land-based dust collectors. The sediment traps were deployed at five ocean sites along a transatlantic transect between northwest Africa and the Caribbean along 12° N, in a down-wind extension of the land-based dust collectors placed at 19° N on the Mauritanian coast in Iwik. In this paper, we lay out the setup of the monitoring experiment and present the particle fluxes from sediment trap sampling over 24 continuous and synchronised intervals from October 2012 through to November 2013. We establish the temporal distribution of the particle fluxes deposited in the Atlantic and compare chemical compositions with the land-based dust collectors propagating to the down-wind sediment trap sites, and with satellite observations of Saharan dust outbreaks. First-year results show that the total mass fluxes in the ocean are highest at the sampling sites in the east and west, closest to the African continent and the Caribbean, respectively. Element ratios reveal that the lithogenic particles deposited nearest to Africa are most similar in composition to the Saharan dust collected in Iwik. Down-wind increasing Al, Fe and K contents suggest a downwind change in the mineralogical composition of Saharan dust and indicate an increasing contribution of clay minerals towards the west. In the westernmost Atlantic, admixture of re-suspended clay-sized sediments advected towards the deep sediment trap cannot be excluded. Seasonality is most prominent near both continents but generally weak, with mass fluxes dominated by calcium carbonate and clear seasonal maxima of biogenic silica towards the west. The monitoring experiment is now extended with autonomous dust sampling buoys for better quantification Saharan dust transport and deposition from source to sink and its impact on fertilization and carbon export to the deep ocean.
    Type: Dataset
    Format: application/zip, 8 datasets
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  • 10
    Publication Date: 2023-09-11
    Keywords: Aluminium, normalized; Biogenic silica; Calcium carbonate; Calcium carbonate, flux; Carbon, inorganic, total; Carbon, organic, total; Carbon, total; DATE/TIME; DEPTH, water; Iron, normalized; M2L; M89; M89_1532_M2-3_L; Meteor (1986); Nitrogen, total; Opal, flux; Organic matter; Organic matter, flux; Potassium, normalized; Residual; Sample code/label; Season; Silicon, normalized; South Atlantic Ocean; Titanium, normalized; Total mass, flux per day; TRAFFIC; Trap, sediment; TRAPS
    Type: Dataset
    Format: text/tab-separated-values, 504 data points
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