Pivaloyl chloride as a new derivatization agent for parabens and its application in simultaneous derivatization and air‑assisted liquid–liquid microextraction of the analytes in hygiene and personal care products
Pivaloyl chloride as a new derivatization agent for parabens and its application in simultaneous derivatization and air‑assisted liquid–liquid microextraction of the analytes in hygiene and personal care products
نویسندگان: محمدرضا افشار مقدم , علی اکبر علیزاده نبیل
کلمات کلیدی: Gas chromatography · Hygiene · Parabens · Derivatization · Air-assisted liquid–liquid microextraction
نشریه: 55363 , 10 , 16 , 2019
| نویسنده ثبت کننده مقاله |
محمدرضا افشار مقدم |
| مرحله جاری مقاله |
تایید نهایی |
| دانشکده/مرکز مربوطه |
مرکز تحقیقات ایمنی غذا و دارو |
| کد مقاله |
68634 |
| عنوان فارسی مقاله |
Pivaloyl chloride as a new derivatization agent for parabens and its application in simultaneous derivatization and air‑assisted liquid–liquid microextraction of the analytes in hygiene and personal care products |
| عنوان لاتین مقاله |
Pivaloyl chloride as a new derivatization agent for parabens and its application in simultaneous derivatization and air‑assisted liquid–liquid microextraction of the analytes in hygiene and personal care products |
| ناشر |
4 |
| 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 |
|
| An air-assisted liquid–liquid microextraction method using of an extraction solvent (less dense than water) has been proposed for simultaneous derivatization and extraction of some p-hydroxybenzoic acid esters (parabens) in diferent samples
before their determination with gas chromatography-fame ionization detection. The analytes are derivatized by a fast reaction occurring between parabens and pivaloyl chloride (as a derivatization agent) and extracted into toluene (as an extraction solvent) under mild conditions in a test tube. After performing the microextraction procedure, a home-made device
(an inverse funnel having a capillary tube) is placed into the tube. A thin flm of the extractant accumulated on the surface
of the aqueous phase is transferred into the capillary part of the device. A fraction of the organic phase is removed by a
microsyringe and injected into the separation system for analysis. Under optimum conditions, detection and quantifcation
limits were between 0.60 and 1.0; and 1.7 and 3.1 ng mL−1 in solution; and 6.0×10−6 and 1.0×10−5; and 1.7×10−5 and
3.1×10−5 g kg−1 in solid, respectively. The enhancement and enrichment factors were obtained in the ranges of 492–650 and
380–410, respectively. Relative standard deviations were less than 6% (n=6) for intra- and less than 9% (n=4) for inter-day
precisions calculated at a concentration of 50 ng mL−1 of each analyte. The calibration graphs were linear with coefcients
of determination≥0.994. Finally, the selected parabens were successfully analyzed in various hygiene and personal care
products by the proposed method. |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| Bakhshizadeh-JICS-2019.pdf | 1398/06/03 | 1274782 | دانلود |