Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Organometallics 2 (1983), S. 305-307 
    ISSN: 1520-6041
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Organometallics 1 (1982), S. 513-517 
    ISSN: 1520-6041
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 39 (1983), S. 1618-1620 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 41 (1985), S. 1545-1547 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 49 (1993), S. 938-940 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 49 (1993), S. 975-976 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' journal of analytical chemistry 366 (2000), S. 48-53 
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract When mercury is quantified by ICP-MS under routine conditions (external calibration) in reference materials, which require mineralization with nitric acid, the experimental concentrations are almost always unacceptably low in comparison to certified values. Sorption of mercury on the Teflon surfaces of the digestion vessels, changes in the viscosity of the aspirated solutions, in the efficiency of the nebulization, in the aerosol transport, and memory effects cannot be responsible for the low results. The intensity of a mercury signal is strongly dependent on the concentration of nitric acid (and other mineral acids) in the measured solutions. Correct results for mercury in the SRM GBW-90101 (Chinese human hair; 2.16 ± 0.21 mg Hg/kg certified) can only be obtained, when the solutions, with which the external calibration curves were established, have exactly the same nitric acid concentration as the aspirated digests (2.03 ± 0.01 mg Hg/kg; n = 5), when mercury is determined by the standard addition method (2.10 ± 0.01 mg Hg/kg; n = 5), or when the experimental mercury concentration obtained at a nitric acid concentration in the digest, different from the concentration in the external calibration solutions, is corrected mathematically based on a pre-established function [Hg2+] = f [HNO3]. The concentrations found by this mathematically based correction 2.04 ± 0.01 mg Hg/kg (n = 5) is in good agreement with the values obtained by acid matched calibration or by the standard addition method. For practical work with large numbers of samples the mathematical correction appears to be the method of choice. For occasional mercury determinations, the standard addition method seems to be the most practicable.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A microwave procedure for the digestion of the NIST 1634b reference material “residual fuel oil” in closed pressurized vessels was developed in an attempt to facilitate routine analysis and obtain reproducible conditions or comparable results. The influence of sample size, reagent composition and volume, microwave power, and duration of heating on the digestion procedure was studied. Pressure and temperature inside the reaction vessels were monitored to determine the progression of the reaction and to develop optimal conditions. A nine-step heating program requiring 36.5 min with microwave power not exceeding 450 W in the pulsed mode was found suitable for the digestion of ∼ 250 mg fuel oil with a mixture of nitric acid (5.0 mL) and hydrogen peroxide (2.0 mL). The reproducibility of microwave power was determined in terms of the relative standard deviations (n = 3) for temperature (2.7%) and pressure (4.9%) data. The vapor pressures obtained with 5.0 mL Milli-Q water (heated) in an 80-mL digestion vessel showed good agreement with literature data. The excess acid in the resulting digests was removed by evaporation and the concentrations of 24 elements (Ag, Al, As, Ba, Bi, Ca, Cd, Co, Cr, Cu, Fe, Hg, Mg, Mo, Ni, Pb, Sb, Sn, Sr, Ti, Tl, V, U, and Zn) were determined in the diluted digests by inductively coupled plasma mass spectrometry (ICP-MS). The experimental results were in good agreement with the certified and recommended concentrations for eight elements (Al, As, Co, Cr, Ni, Pb, V, Zn) in solutions obtained after one digestion step. An additional digestion step, consisting of intermediate cooling and venting stages, was required for the accurate determination of Fe. No agreement was reached for Ca and Ba even after two-step digestion. The proposed method of digestion provided precise results with relative standard deviations generally less than 5% for most of the elements determined.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' journal of analytical chemistry 359 (1997), S. 434-437 
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A three-organism food chain within a rock pool at Rosedale, NSW, Australia, was investigated with respect to arsenic compounds by high performance liquid chromatography – hydraulic high pressure nebulization – inductively coupled plasma mass spectrometry (HPLC-HHPN-ICP-MS). Total arsenic concentration was determined in the seaweed Hormosira banksii (27.2 μg/g dry mass), in the gastropod Austrocochlea constricta (74.4 μg/g dry mass), which consumes the seaweed, and in the gastropod Morula marginalba (233 μg/g dry mass), which eats Austrocochlea constricta. The major arsenic compounds in the seaweed were (2′R)-dimethyl[1-O-(2′,3′-dihydroxypropyl)-5-deoxy-β-d-ribofuranos-5-yl]arsine oxide and an unidentified compound. The herbivorous gastropod Austrocochlea constricta transformed most of the arsenic taken up with the seaweed to arsenobetaine. Traces of arsenite, arsenate, dimethylarsinic acid, arsenocholine, the tetramethylarsonium cation, and several unknown arsenic compounds were detected. Arsenobetaine accounted for 95% of the arsenic in the carnivorous gastropod Morula marginalba. In Morula marginalba the concentration of arsenocholine was higher, and the concentrations of the minor arsenic compounds lower than in the herbivorous gastropod Austrocochlea constricta.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 319 (1984), S. 556-559 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary Samples of approximately 1.0 g were taken from three Texas lignite cores and mineralized in oxygen bombs. The residue was dissolved in distilled water to a total volume of 50 ml. The resulting solutions were analyzed for fluoride by ion chromatography and with a fluoride-sensitive electrode. The results obtained with these two methods were in good agreement. The pH of solutions prepared from mineralized lignite samples must be adjusted to fall into the range 4 to 12 before fluoride is determined by ion chromatography. The calibration curve is linear to 10 mg/l F− (in solution). Twenty μg/l of F− (in solution) corresponding to 1 mg/kg of dry lignite can still be determined. Ion chromatography has higher sensitivity for fluoride than fluoride-sensitive electrodes and provides at the same time information about other anionic species. The fluorine concentrations in the three cores varied from 10 to 140 mg/kg (dry lignite). Layers of clay interspersed between the lignite seams had higher fluorine concentrations than the lignite.
    Notes: Zusammenfassung Braunkohlenproben von etwa 1 g wurden in der Sauerstoffbombe mineralisiert, der Rückstand in Wasser gelöst und die Lösung mit Hilfe der Ionen-Chromatographie und mit einer fluoridsensitiven Elektrode auf Fluorid untersucht. Die mit beiden Methoden erhaltenen Ergebnisse stimmten gut überein. Vor der Ionen-Chromatographie müssen die Lösungen der mineralisierten Proben auf pH 4–12 eingestellt werden. Die Eichkurve verläuft bis 10 mg/l F− linear. Noch 20 μg/l F− (in Lösung), entsprechend 1 mg/kg trockener Braunkohle, können bestimmt werden. Die Ionen-Chromatographie weist eine höhere Empfindlichkeit auf als fluorid-sensitive Elektroden und bietet darüber hinaus Information über andere Anionen. Die untersuchten Fluoridkonzentrationen lagen zwischen 10 und 140 mg/kg (trockene Braunkohle). Zwischengelagerte Lehmschichten wiesen höhere Fluorgehalte auf.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...