کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1200874 1493506 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Rapid screening of edible oils for phthalates using phase-transfer catalyst-assisted hydrolysis and liquid phase microextraction coupled to high performance liquid chromatography–tandem mass spectrometry
ترجمه فارسی عنوان
غربالگری سریع روغن های خوراکی برای فتالات با استفاده از هیدرولیز فاز انتقال کاتالیزور و میکرو اکستراکسیون مایع فاز همراه با کروماتوگرافی مایع کروماتوگرافی با عملکرد بالا طیف سنجی جرمی
کلمات کلیدی
کل فتالات اسید فتالیک، تترابوتیل آمونیوم برومید، روغن خوراکی، کاتالیزور انتقال فاز
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• A rapid screening method for phthalates (PAEs) in edible oil was developed.
• Hydrolysis of PAEs was completed in 10 min due to use of a phase-transfer catalyst.
• The resulting phthalic acid was retrieved with 600 μL of tributyl phosphate.
• Quantification of the acid was conducted by HPLC–MS/MS in 6 min.
• The method presented a promising methodology to deal with oil matrices.

Edible oil is easily contaminated with phthalic acid esters (PAEs). Conventional procedures to analyze individual PAEs require very rigorous experimental conditions that are extremely labor-intensive due to significant procedural contaminations generated by the ubiquitous presence of PAEs in the laboratory environment. In this study, a rapid screening method for PAEs in edible oil was successfully developed. Using a phase-transfer catalyst (terabutylammonium bromide) during oil/water biphasic base hydrolysis of PAEs, the hydrolysis time was decreased from a previously reported time of 20 h to 10 min (80 °C). The resulting phthalic acid in the acidified hydrolysate was extracted with 600 μL of tributyl phosphate and then analyzed by high performance liquid chromatography–tandem mass spectrometry in 6 min. Parameters affecting the hydrolysis of PAEs and the extraction of phthalic acid were optimized, and the analytical method was validated. No obvious matrix effect existed in the edible oils whether an external or internal standard method was used. The detection limit was 1.0 μmol kg−1, and the quantification limit was 1.3 μmol kg−1. The recovery rates varied from 86 to 107% with relative standard deviations equal to or lower than 9.9% in all of the tested conditions. Twenty-six samples were analyzed, and the background corrected total PAE content was found to be in the range of

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography A - Volume 1420, 13 November 2015, Pages 26–34
نویسندگان
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