کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1162911 1490905 2016 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Design and testing of a new sampler for simplified vacuum-assisted headspace solid-phase microextraction
ترجمه فارسی عنوان
طراحی و آزمایش یک نمونه جدید برای ساده سازی مایکروکساکتیو فاز جامد فاز فشرده سازی خلاء
کلمات کلیدی
فیکساسیون فاز جامد فشاری خلاء، نمونه سوپاپ گاز بیفینیل های پلی کربنات، تجزیه و تحلیل آب
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• We describe a new, low-cost and simplified gastight sampler for Vac-HSSPME.
• All Vac-HSSPME operations are performed through the septum of one port.
• The device is tested for the water analysis of polychlorinated biphenyls.
• Very good sensitivity achieved within short sampling times and mild conditions.

The design and testing of a new and low-cost experimental setup used for vacuum-assisted headspace solid-phase microextraction (Vac-HSSPME) is reported here. The device consists of a specially designed O-ring seal screw cap offering gas-tight seal to commercially available headspace vials. The new polytetrafluoroethylene (PTFE) cap was molded by a local manufacturer and had a hole that could tightly accommodate a septum. All operations were performed through the septum: air evacuation of the sampler, sample introduction and HSSPME sampling. The analytical performance of the new sampler was evaluated using 22 mL headspace vials with 9 mL water samples spiked with polychlorinated biphenyls (PCBs). Several experimental parameters were controlled and the optimized conditions were: 1000 rpm agitation speed; 30 min extraction time; 40 °C sampling temperature; polydimethylsiloxane-divinylbenzene (PDMS-DVB) fiber. The lack of accurate Henry's law constant (KH) values and information regarding how they change with temperature was a major limitation in predicting the phase location of evaporation resistance during Vac-HSSPME. Nevertheless, the combined effects of system conditions indicated the increasing importance of gas phase resistance with increasing degree of PCBs chlorination. Stirring enhancements were not recorded for the higher chlorinated PCBs suggesting that the hyperhydrophobic gas/water interface was the preferred location for these compounds. Analytically, the developed method was found to yield linear calibration curves with limits of detection in the sub ng L−1 level and relative standard deviations ranging between 5.8 and 14%. To compensate for the low recoveries of the higher chlorinated PCB congeners in spiked river water the standard addition methodology was applied. Overall, the compact design of the new and reusable sample container allows efficient HSSPME sampling of organic analytes in water within short extraction times and at low sampling temperatures compared to other published HSSPME methods.

Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Analytica Chimica Acta - Volume 927, 13 July 2016, Pages 46–54
نویسندگان
, , ,