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  • 1
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract An analytical procedure for speciation of As in urban aerosol samples was developed. The aerosols were collected by sequential filtration through membrane filters. Part of each filter was investigated by INAA for the total amount of As. Another part of the filters was treated by a sequential extraction procedure to differentiate between water-extractable, phosphate-extractable and refractory chemical forms. Water-extractable forms were further differentiated into anionic As species by HPLC-HGAFS. Extractability of As into water exhibited a clear dependency on the aerosol size fraction (12% in coarse fraction and 50% in fine fraction). Dependency of the phosphate extractable As on the aerosol size fraction seems not to be significant (10–15% in both size fractions). The remaining amount, i.e., about 78% of the coarse As and about 40% of the fine As was considered to be refractory or environmentally immobile As. Water-extractable As forms could only be attributed to arsenate.
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  • 2
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract The concentration levels of total iodine obtained by RNAA in different sorts of tobacco, including the reference sample Kentucky Tobacco 2RI, two new candidate reference materials, Oriental Tobacco Leaves /CTA-OTL-1/ and Virginia Tobacco Leaves /CTA-VTL-2/ prepared in the Institute of Nuclear Chemistry and Technology, Warsaw, and some biological SRMs, are presented and discussed.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 338 (1990), S. 559-561 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The greater part of essential iodine enters living organisms via the food chain. Nevertheless, quantitative data on its concentration in diets, food articles and also in available SRMs are very poor and scarce. This and WHO recommendations on daily allowances of iodine for man via food articles caused an added demand for accurate and reliable determination of iodine in these samples. From this point of view the purpose of the present was to analyse and to establish the concentration levels of total iodine in some food articles, diets, SRMs and candidate reference materials by the use of rapid radiochemical separation, developed in our laboratory. The results were checked by the analysis of SRMs with available certified values for iodine and good agreement is evident.
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  • 4
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract On the basis of tracer experiments, a simple and rapid radiochemical separation method for simultaneous determination of I−, Br− and Cl− in one aliquot of a water sample (only 2–4 ml) has been developed. The method is based on short irradiation of the water sample and separation of the halogens using sequential ion exchange columns filled with Dowex 1×8, 100–200 mesh anionic resin prepared in I−/I2, Br−/Br2 and Cl− form. After washing the columns with an appropriate volume of 2% NaCl solution, the resins were transferred to vials and activities of the isolated radionuclides128I,82Br and38Cl measured together with standards in a “well type” or on a coaxial Ge detector connected to a Canberra 90 multichannel analyzer. Besides high chemical yields, from the γ-spectra of the isolated radionuclides, it is evident that high decontamination fac-
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 173 (1993), S. 357-364 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Inorganic arsenic, MMA, DMA and arsenobetaine (Asβ) were separated by the use of cation and anion exchange chromatography combined with neutron activation. Two complementary approaches were used: firstly, authentic, non-irradiated arsenic compounds, either singly or in mixtures, were separated and NAA of the fractions used as an element specific detection method. Secondly, the arsenic compounds were neutron irradiated under different conditions and for different times and the products separated and quantified. The76As labeled species (mono-, di and trimethylated) were then additionally used to calibrate and improve the column separations. Using the separations developed, arsenic species in samples of shrimps and the standard reference material DORM-1 were determined, after an extraction step, using ion exchange chromatography followed by INAA of the fractions collected.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 9 (1995), S. 305-313 
    ISSN: 0268-2605
    Keywords: arsenic species ; mushrooms ; methylarsonic acid ; dimethylarsinic acid ; tetramethylarsonium ion ; arsenobetaine ; arsenite ; arsenate ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Arsenic species in arsenic accumulating mush- rooms (Sarcosphaera coronaria, Laccaria amethystina, Sarcodon imbricatum, Entoloma lividum, Agaricus haemorrhoidaius, Agaricus placomyces, Lycoperdon perlatum) were determined. HPLC/ICP MS and ion-exchange chromatogra- phy-instrumental neutron activation analysis (NAA) combinations were used. The remarkable accumulator Sarcosphaera coronaria (up to 2000 mg As kg-1 dry wt) contained only methylarsonic acid, Entoloma lividum only arsenite and arsenate. In Laccaria amethystina dimethylarsinic acid was the major arsenic compound. Sarcodon imbricatum and the two Agaricus sp. were found to contain arsenobetaine as the major arsenic species, a form which had previously been found only in marine biota. Its identification was confirmed by electron impact MS.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 11 (1997), S. 673-682 
    ISSN: 0268-2605
    Keywords: arsenic species ; mushrooms ; methylarsonic acid ; dimethylarsinic acid ; tetramethylarsonium ion ; arsenobetaine ; arsenocholine ; arsenite ; arsenate ; trimethylarsine oxide ; HPLC-ICP-MS ; taxonomy ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In 50 mushroom species (56 samples) from Slovenia, Switzerland, Brazil, Sweden, The Netherlands and USA, total arsenic was determined by radiochemical neutron activation analysis (RNAA). Arsenic concentrations ranged from 0.1 to 30 μg g-1 (dry mass). Arsenic compounds were determined in methanol extracts from the mushrooms by HPLC-ICP-MS. The aim of the study was not only to quantify arsenic compounds in mushrooms but also to uncover trends relating the methylating ability of a mushroom to its taxonomic or evolutionary status.The main arsenic compound found in many mushrooms (various puffballs, Agaricales and Aphyllophorales) was arsenobetaine. Arsenate [As(V)] was the main arsenic species in Laccaria fraterna and Entoloma rhodopolium and arsenite [As(III)] in Tricholoma sulphureum. A mixture of arsenite and arsenate was present in Amanita caesarea. Dimethylarsinic acid (DMA) and methylarsonic acid were present in many mushrooms, but generally as minor components. In Laccaria laccata, Leucocoprinus badhamii and Volvariella volvacea, DMA was the major metabolite. Arsenocholine (AC) and the tetramethylarsonium ion were present in a few species, generally at low concentrations, except for Sparassis crispa, in which AC was the main compound. Tri- methylarsine oxide was not found in any of the mushrooms. In some species small amounts of unknown compounds were also present. The possible taxonomic significance of the metabolite patterns and the predominance of arsenobetaine in more advanced fungal types are discussed. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 354 (1996), S. 592-595 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Arsenic compounds have been determined in some environmental samples from the German Environmental Specimen Bank (ESB) (marine mussels, freshwater mussel and fish, sea-gull eggs) and certified reference materials (DORM-1, DOLT-1, NBS Oyster Tissue) after separation by open column cation and anion exchange chromatography by two different methods of total arsenic determination in separated fractions (instrumental neutron activation analysis or hydride generation atomic absorption spectrometry). Arsenobetaine has been identified as the major species in all the different materials.
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  • 9
    Publication Date: 1993-10-01
    Print ISSN: 0236-5731
    Electronic ISSN: 1588-2780
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Published by Springer
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  • 10
    Publication Date: 1990-01-01
    Print ISSN: 0937-0633
    Electronic ISSN: 1432-1130
    Topics: Chemistry and Pharmacology
    Published by Springer
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