In-process prepared deep eutectic solvent based homogeneous liquid–liquid microextraction for the determination of irgaphos 168 and irganox 1010 in polypropylene packed drinks

In-process prepared deep eutectic solvent based homogeneous liquid–liquid microextraction for the determination of irgaphos 168 and irganox 1010 in polypropylene packed drinks


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دانشگاه علوم پزشکی تبریز
دانشگاه علوم پزشکی تبریز

نویسندگان: محمدرضا افشار مقدم , مریم نائبی

کلمات کلیدی: deep eutectic solvents, homogeneous liquid–liquid microextraction, irganox 1010, irgaphos 168, polypropylene package

نشریه: 55358 , 14 , 43 , 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 73038
عنوان فارسی مقاله In-process prepared deep eutectic solvent based homogeneous liquid–liquid microextraction for the determination of irgaphos 168 and irganox 1010 in polypropylene packed drinks
عنوان لاتین مقاله In-process prepared deep eutectic solvent based homogeneous liquid–liquid microextraction for the determination of irgaphos 168 and irganox 1010 in polypropylene packed drinks
ناشر 5
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 situ synthesis of a deep eutectic solvent and homogeneous liquid–liquid microextraction performed in a narrow bore tube was developed for efficient extraction of irgaphos 168 and irganox 1010 in doogh and water samples packed in polypropylene packages. First, pH of the aqueous sample solutions containing the analytes is adjusted at 9. Then a hydrogen bond acceptor (choline chloride) and a hydrogen bond donor (oleic acid) are dissolved in the solution and vortexed to obtain a homogeneous solution. The solution is filled into a narrow bore tube, in which its bottom was clogged by a septum. Then hydrochloric acid solution is injected into the solution by a syringe. The tube is placed in an ultrasonic bath. During this step, the droplets of choline chloride:oleic acid deep eutectic solvent are produced. The method indicated high enrichment factor (435 for irgaphos 168 and 488 for irganox 1010), low limits of detection (0.03 and 0.09 ng/mL for irgaphos 168 and irganox 1010, respectively) and quantification (0.13 and 0.29 ng/mL for irgaphos 168 and irganox 1010), good recovery (74 and 83% for irgaphos 168 and irganox 1010, respectively), and satisfactory repeatabilities (relative standard deviations ≤12%) can be obtained using the developed method.

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نویسنده نفر چندم مقاله
محمدرضا افشار مقدمپنجم
مریم نائبیاول

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JSS-Jamshidi-Abolhassani.pdf1399/05/091182665دانلود