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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' journal of analytical chemistry 366 (2000), S. 846-850 
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In order to determine PAHs in marine sediment samples by GC/MS(SIM) a new extraction approach of ASE-SFE was evaluated using combined accelerated solvent extraction (ASE, dynamic and static mode) and supercritical fluid extraction (SFE, dynamic mode) without further purification of the sample. The solvents used for ASE-SFE were methylene chloride and carbon dioxide. The recovery data, precision and accuracy of the whole method were evaluated statistically. The average recoveries of PAHs, based on deuterated internal standards were 77% for 2–3-ring PAHs, 85% for 4-ring PAHs, 88% for ¶5-ring PAHs and 97% for 6-ring PAHs. The extraction time required for the ASE-SFE technique was 30 min, which is longer than in the case of independent use of ASE and shorter compared to SFE. ASE-SFE recoveries of PAHs from SRM marine sediment are comparable for (2–3-ring, 4-ring PAHs) or higher (5-ring, 6-ring PAHs) than reported for the conventional extraction methods of ASE and SFE. Method detection limits of (MDL) were statistically estimated. MDL values obtained for 15 PAHs compounds vary between 0.06 ngg−1 and 3.54 ngg−1.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-515X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The origin and temporal variation in composition of sedimented particulate organic matter (POM) in the Gulf of Trieste (northern Adriatic) was studied over the year with special reference to the composition and sedimentation of macroaggregates in summer of 1991 using sediment traps. Suspended and sedimented POM, comprising a minor part of the largely inorganic total particulate matter, was prevalently of marine origin and composed mostly of humic substances followed by carbohydrates and proteins. Seasonal variations of particulate proteins and carbohydrates were correlated with variations of phytoplankton biomass. ‘New’ production, occurring in late spring as a consequence of massive riverine inputs of N, Si and P nutrients in the surface layer of the Gulf, produced high particulate carbohydrate and protein concentrations. Subsequent depletion of introduced nutrients caused the decrease of particulate protein concentration but not that of particulate carbohydrate. The prolonged plankton biosynthesis of carbohydrates successively produced marine snow and later macroaggregates. The macroaggregates were characterized by δ13C value of −19.9‰. and their carbohydrates were mostly composed of glucose followed in decreasing order by mannose, fructose, galactose, arabinose, ribose, xylose and fucose, suggesting a prevalent origin from phytoplankton structural heteropolysaccharides. Sedimentation of particulate organic constituents in the summertime, characterized by the massive presence of macroaggregates in the surface layer above the pycnocline, was the highest at a depth of 10 m at the end of this phenomenon, about six weeks after its first appearance. Sedimented macroaggregates were clearly traced by a characteristic δ13C signal and higher carbohydrate concentrations. The monosaccharide composition was influenced by selective degradation in the water column. Sedimented POM in the bottom layer was, on the other hand, more affected by sediment resuspension. The mean yearly decrease of particulate protein-C and carbohydrate-C by 40–50% in the water column between the depths of 10 and 20 m indicates the preferential utilization of these constituents by microorganisms. The decrease of particulate humic-C is probably more the result of the export of particulate matter from the Gulf. This study also indicates that the macroaggregate formation has little impact on the annual C and N budget in such coastal areas.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 348 (1994), S. 650-653 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A fast one-step technique has been developed for the resolution of hydrocarbons into aromatics, olefines and saturates. The analyser consists of three branches with different capillary restrictions, specific absorbers and delayers, and can be applied to gaseous or liquid samples of hydrocarbons with a boiling point of up to 220°C. The time required for an analysis under optimal conditions is 6 min. The analyser is installed directly in the oven of the gas chromatograph, using a single flame ionisation detector. It was tested by selected hydrocarbons occurring in gasoline in significant amounts in different concentration ranges. Leaded and unleaded commercial gasolines were examined as real samples. The method had been successfully applied to the fast identification of hydrocarbons in the case of fuel spills.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 341 (1991), S. 720-722 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A simple and rapid head space gas-chromatographic method for the determination of residual ethylene oxide in surfactants used in shampoos and other cosmetic products is described. The analyte was determined in various materials in the concentration range between 0.1 and 10 μg/g and sufficient linearity of response was observed to allow use of the calibration line and/or the standard addition method (r≥0.977). In comparison with extraction and adsorption procedures for sampling of ethylene oxide prior to analysis, the head space technique is faster and more accurate but suffers in precision. Coefficients of variation by the interpolation of the calibration line of 10% to 30% are typical for standard solutions in methylene chloride and real samples. Better precision was obtained by the standard addition method.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Die elektromotorische Kraft von Konzentrationsketten des Typs (Pt) H2/Polystyrolälfonsäure Polystyrolsulfonsäure/H2 (Pt) mit Flüssigkeitsverbindung wurde im Molalitätsbereich von 0,1 bis 0,001 (bezogen auf Monomereinheiten) gemessen. Die aus diesen Messungen folgenden Werte für den mittleren Aktivitätskoeffizienten wurden mit den auf Basis eines Stäbehenmodells errechneten verglichen. Dabei ergab sich eine sehr gute Übereinstimmung zwischen Theorie und Experiment.
    Notes: The electromotive force of the concentration cell (Pt) H2/polystyrenesulphonic acid polystyrenesulphonic acid/H2 (Pt) with liquid-liquid junction was measured in the concentration range of the polystyrenesulphonic acid from 0.1 to 0.001 monomolal. The values of the mean activity coefficient, derived from these measurements, were compared with those calculated on the basis of the rodlike model. A very good agreement between theory and Zxperiment has been found.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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