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  • elektrochem. Detektor  (2)
  • 4-Aminoantipyrine derivatives of phenols  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 28 (1989), S. 465-468 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Chlorinated phenols ; 4-Aminoantipyrine derivatives of phenols ; Metabolites of phenoxy alkanoic acid herbicides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary High performance liquid chromatography (HPLC) has been applied to the separation and determination of o-chlorophenol, 2,4-dichlorophenol, 3,4-dichlorophenol, 2,5-dichlorophenol, and 2,4,5-trichlorophenol in water samples after prior derivatization with 4-aminoantipyrine. These substances are the phenolic decomposition products of the phenoxy-alkanoic acid herbicides: 2,4-dichlorophenoxyacetic acid (2,4-D), 2,4-dichlorophenoxybutyric acid (2,4-DB), and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T). An RP-C18 column was used, with gradient elution starting at 50/50 and changing to 70/30 methanol/water (v/v) after 24 min. Detection was carried out at 470 nm where the 4-aminoantipyrilquinonimine derivatives show maximum absorbance. The method was linear over a concentration range of 5–10,000 ppb phenol in the original water sample. By using an enrichment step a detection limit of 2 ppb phenol could be approached. The method was used to study the degree of degradation of the phenoxy acids to phenols under different conditions of temperature, pH, and UV irradiation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 309 (1981), S. 8-12 
    ISSN: 1618-2650
    Keywords: Best. von Methomyl, Methomyl-oxim in Obst und Wasser ; Chromatographie, HPLC ; elektrochem. Detektor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary A simple and specific quantitative HPLC method for the analysis of methomyl residues in fruit crops and water is described. The method is based on simple extraction steps, high-performance liquid chromatographic separation using a reversed phase column (RP-C18) and UV detection. With this analytical system, methomyl residues at 1 ng/g level can be detected. This approach allows also the simultaneous determination of methomyl and its degradation product methomyl-oxime. This is possible either by using the UV detector at 233 nm or by using both the UV- and the electrochemical detectors in series. Using this combined detection system, it was possible to determine methomyl at the 1 ng/ml level and methomyl-oxime at the 100 pg/ml level in water. Recovery rate in the range of 0.01–1 μg/g is 101.4±6% in fruit crops (apples) and 93.7±4% in water.
    Notes: Zusammenfassung Es wird eine hochleistungs-flüssigkeits-chromatographische Methode zur quantitativen Bestimmung der Methomylrückstände in Obst und Wasser beschrieben, mit der noch Rückstandsmengen von 1 ng/g (ppb) erfaßbar sind. Das Verfahren besteht aus einem Extraktionsschritt, Aufreinigungsschritt, der Trennung der Rückstände auf einer Umkehrphase (RP-C18) und der UV-Detektion. Die Methode ermöglicht die gleichzeitige Bestimmung von Methomyl und seinem Hydrolyseprodukt (Methomyl-oxim) durch die Anwendung des UV-Detektors allein oder durch zusätzliche elektrochemische Detektion. Durch diese Schaltanordnung wurden Konzentrationen von 1 ng/ml Methomyl und 100 pg/ml (ppt) Methomyl-oxim in Wasser bestimmt. Die Methode gestattet im Bereich von 0,01–1 μg/g eine Wiederfindungsrate von 101,4±6% in Obst (Äpfel) und 93,7±4% in Wasser.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 307 (1981), S. 382-384 
    ISSN: 1618-2650
    Keywords: Best. von Sulfonamiden, Sulfadiazin, Sulfadimidin in Milch ; Chromatographie, HPLC ; elektrochem. Detektor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary A simple quantitative method for the analysis of the residues of sulphadiazine and sulphadimidine in milk is described. The method is based on a simple extraction step and high-performance liquid chromatography (HPLC) with electrochemical detection. The Chromatographic seperation is performed on a reversed phase column (RP-C2) and an aqueous eluent. With this analytical system 10 ng/ml can be detected. Recoveries of sulphonamides from milk are between 94.4% and 110% in the concentration range of 0.01–1.8 μg/ml sample.
    Notes: Zusammenfassung Es wird eine einfache Methode zum Nachweis von Sulfonamidrückständen in Milch am Beispiel von Sulfadiazin und Sulfadimidin beschrieben, mit der noch Rückstandsmengen von 10 ng/ml erfaßbar sind. Das Verfahren besteht aus einem einfachen Aufreinigungsschritt, der Trennung der Rückstände auf einer Umkehrphase (RP-C2) und der Detektion mit einem elektrochemischen Detektor. Die Wiederfindungsraten liegen zwischen 94,4% und 110% für einen Konzentrationsbereich von 0,01–1,8 μg/ml Untersuchungsmaterial.
    Type of Medium: Electronic Resource
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