کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1241956 1495800 2015 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Screen-printed electrode based electrochemical detector coupled with ionic liquid dispersive liquid–liquid microextraction and microvolume back-extraction for determination of mercury in water samples
ترجمه فارسی عنوان
الکترودهای آشکارساز الکترود بر روی صفحه نمایش همراه با میکروسکاشی مایع پراکنده مایع منی و استخراج برگشتی میکرووولوم برای تعیین جیوه در نمونه های آب
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• Mercury determination in environmental and drinking waters.
• DLLME and microvolume back-extraction in sample preparation.
• Gold nanostructurated screen-printed carbon electrode based electrochemical detector.
• Electrochemical sensor as detection system for liquid-phase microextraction.
• Limit of detection lower than other previous works using screen-printed electrodes.

A novel approach is presented, whereby gold nanostructured screen-printed carbon electrodes (SPCnAuEs) are combined with in-situ ionic liquid formation dispersive liquid–liquid microextraction (in-situ IL-DLLME) and microvolume back-extraction for the determination of mercury in water samples. In-situ IL-DLLME is based on a simple metathesis reaction between a water-miscible IL and a salt to form a water-immiscible IL into sample solution. Mercury complex with ammonium pyrrolidinedithiocarbamate is extracted from sample solution into the water-immiscible IL formed in-situ. Then, an ultrasound-assisted procedure is employed to back-extract the mercury into 10 µL of a 4 M HCl aqueous solution, which is finally analyzed using SPCnAuEs.Sample preparation methodology was optimized using a multivariate optimization strategy. Under optimized conditions, a linear range between 0.5 and 10 µg L−1 was obtained with a correlation coefficient of 0.997 for six calibration points. The limit of detection obtained was 0.2 µg L−1, which is lower than the threshold value established by the Environmental Protection Agency and European Union (i.e., 2 µg L−1 and 1 µg L−1, respectively). The repeatability of the proposed method was evaluated at two different spiking levels (3 and 10 µg L−1) and a coefficient of variation of 13% was obtained in both cases. The performance of the proposed methodology was evaluated in real-world water samples including tap water, bottled water, river water and industrial wastewater. Relative recoveries between 95% and 108% were obtained.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Talanta - Volume 135, 1 April 2015, Pages 34–40
نویسندگان
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