Development of an ultrasonic-assisted and effervescent tablet-assisted dispersive liquid–liquid microextraction based on ionic liquids for analysis of benzoylurea insecticides

Development of an ultrasonic-assisted and effervescent tablet-assisted dispersive liquid–liquid microextraction based on ionic liquids for analysis of benzoylurea insecticides


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نویسندگان: محمدرضا افشار مقدم

کلمات کلیدی: Benzoylurea insecticides; effervescentassisted dispersive liquid– liquid microextraction; ionic liquid; high-performance liquid chromatography; fruit juices; vegetables

نشریه: 15130 , 0 , 0 , 2020

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نویسنده ثبت کننده مقاله محمدرضا افشار مقدم
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات ایمنی غذا و دارو
کد مقاله 73935
عنوان فارسی مقاله Development of an ultrasonic-assisted and effervescent tablet-assisted dispersive liquid–liquid microextraction based on ionic liquids for analysis of benzoylurea insecticides
عنوان لاتین مقاله Development of an ultrasonic-assisted and effervescent tablet-assisted dispersive liquid–liquid microextraction based on ionic liquids for analysis of benzoylurea insecticides
ناشر 3
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ خیر
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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In this work, an effervescent tablet containing ionic liquids was madeand used in ultrasonic-assisted dispersive liquid–liquid microextractionfor extraction and preconcentration of benzoylurea insecticides (hexa-flumuron, teflubenzuron, triflumuron and chlorfluazuron) in fruit juiceand vegetable sample prior to high-performance liquid chromatogra-phy-diode array detection. In this method, the effervescent tabletcomposed of sodium bicarbonate, tartaric acid and potassium bromideis used for dispersion of an extraction solvent into an aqueous phasecontaining the analytes. An ionic liquid (1-butyl-3-methylimidazoliumhexafluorophosphate) is used as the extraction solvent. An acid–basereaction between tartaric acid and sodium bicarbonate is immediatelyoccurred, after releasing the tablet into the aqueous phase, and theproduced CO2leads to dispersion of the extraction solvent (placed inthe tablet) into the solution as tiny droplets. Also, sonication is used inthe improvement of dispersion of the extraction solvent and masstransfer of the analytes into the tiny droplets of the extraction solvent.Under the optimum conditions, limits of detection and quantificationwere obtained in the ranges of 0.04–0.19 and 0.13–0.64 ng mL–1,respectively. The enrichment factors and extraction recoveries of theselected analytes ranged from 370 to 465 and 74% to 93%, respectively.The relative standard deviations were≤6.9% for intra-day (n = 6) andinter-day (n = 5) precisions at a concentration of 1 ng mL–1of eachanalyte. Finally, some fruit juice and vegetable samples were effectivelyanalysed by the proposed method, and hexaflumuron was found incabbage sample, at ng g−1concentration range

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