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2 protocols using diniconazole

1

Multianalyte Pesticide Extraction and Quantification

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All the target compounds (chlorpyrifos, haloxyfop-R-methyl, oxadiazon, diniconazole, clodinafop-propargyl, fenpropathrin, and fenoxprop-P-ethyl) with purity >98% were procured from Dr Ehrenstorfer (Agsburg, Germany). Sodium sulfate, potassium chloride, sodium chloride, sodium hydroxide, acetonitrile (ACN), acetone, hydrochloric acid (37%, w/w), and methanol (analytical grade) were obtained from Merck (Darmstadt, Germany). 2-Propanol was acquired from Caledon (Georgetown, Canada). Deionized water was supplied from Ghazi Co. (Tabriz, Iran). Extraction solvents including 1,1,2-trichloroethane (1,1,2-TCE), 1,1,1-trichloroethane (1,1,1-TCE), 1,2-dibromoethane (1,2-DBE), and carbon tetrachloride were purchased from Janssen (Beerse, Belgium). To synthesize the adsorbent, nickel(ii) chloride hexahydrate (NiCl2·6H2O), 1,4-benzenedicarboxylic acid (1,4-BDCA), and concentrated ammonia solution (25%, w/w) were purchased from Merck (Darmstadt, Germany). A mixture standard solution including 250 mg L−1 of each pesticide was provided in methanol and diluted using deionized water for daily-used solutions of interest.
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2

Analytical Standards of Triazole Fungicides

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All chromatography-grade solvents including acetonitrile, methanol, ethanol and propanol were purchased from Merck KGaA, Germany. Sodium dodecyl sulfate (SDS) was obtained from Merck Schuchardt OHG, Germany. Cetyltrimethylammonium bromide (CTAB) and sodium dodecylbenzene sulfonate (SDBS) were obtained from Sigma-Aldrich, Germany. The analytical standards of triazole including myclobutanil, triadimefon, tebuconazole, hexaconazole and diniconazole were purchased from Dr Ehren-storfer GmbH, Germany. Stock standard solution of each triazole fungicide (1000 μg mL−1) was prepared by dissolving an appropriate amount in methanol and stored at 4 °C. Working standard solutions was prepared by diluting the stock standard solution with water. Deionized water (Millipore Waters, USA) with the resistivity of 18.2 MΩ cm was used throughout the experiments.
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