کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1198966 1493492 2016 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Core–shell electrospun polybutylene terephthalate/polypyrrole hollow nanofibers for micro-solid phase extraction
ترجمه فارسی عنوان
نانو فیبرهای توخالی پلی اتیلن تیرفتالیت / پلیپیرلور الکترو اسپور کروی برای استخراج فاز میکرو جامد
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• A core–shell polyvinylpyrrolidone-polybutylenetephthalate/polypyrrole nanofibers—based sorbent was electrospun.
• Polyvinylpyrrolidone as the core moiety was removed and the desired hollow nanofibers as a sorbent fabricated.
• Immersed μ-solid phase extraction along with GC–MS was used for trace determination of triazines.

In the present work, a new micro-solid phase extraction (μ-SPE) sorbent as an extracting medium based on core–shell nanofibers was synthesized by electrospinning. The core–shell nanofibers of polyvinylpyrrolidone-Polybutylene terephthalate/polypyrrole (PVP-PBT/PPy) were electrospun and subsequently, modified hollow nanofibers were prepared by removing the central PVP moiety. Moreover, conventional PBT/PPy was also prepared for the comparison purposes. The homogeneity and the porous surface structure of the core–shell nanofibers were confirmed by scanning electron microscopy (SEM). The applicability of the fabricated nanofibers-coating was examined by immersed μ-SPE of some selected triazine herbicides from aqueous samples and wheat grains. Subsequently, the extracted analytes were transferred into a gas chromatography (GC) after solvent desorption. Influencing parameters on the morphology of nanofiber such as elctrospinning parameters and the weight ratio of components were optimized. In addition, effects of different parameters influencing the extraction efficiency including extraction temperature, extraction time, ionic strength, sample pH, desorption temperature, and desorption time were investigated and optimized. Eventually, the developed method was validated by gas chromatography–mass spectrometry (GC–MS). At the optimum conditions, the relative standard deviation values for real water samples spiked with the selected triazines at 1 ng mL−1 were 4–8% (n = 3) and the limits of detection for the studied compounds were between 50 and 90 ng L−1. The calibration curves for the selected triazines were in the range of 0.3–500 ng mL−1 and regression coefficients (R2) were between 0.9985 and 0.9996.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Chromatography A - Volume 1434, 19 February 2016, Pages 19–28
نویسندگان
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