کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1241928 1495799 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Sequential Injection Chromatography with post-column reaction/derivatization for the determination of transition metal cations in natural water samples
ترجمه فارسی عنوان
کروماتوگرافی تزریقی متوالی با واکنش / مشتقات پس از ستون برای تعیین کاتدی های فلز گذرا در نمونه های آب طبیعی
کلمات کلیدی
کروماتوگرافی تزریق متوالی، کاتیات فلز گذرا، واکنش پس از ستون، تشخیص اسپکتروفتومتریک، انباشته شدن روی ستون
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• A simple sequential injection chromatography (SIC) system was set up.
• Post-column chromogenic reagent addition was carried out for the first time in SIC.
• Separation of transition metal cations on a modified latex guard column was performed.
• Simplex optimization of reagent and mobile phase and analyte stacking were performed.
• Applicability to real sample analysis was demonstrated.

In this work, the applicability of Sequential Injection Chromatography for the determination of transition metals in water is evaluated for the separation of copper(II), zinc(II), and iron(II) cations.Separations were performed using a Dionex IonPACTM guard column (50 mm×2 mm i.d., 9 µm). Mobile phase composition and post-column reaction were optimized by modified SIMPLEX method with subsequent study of the concentration of each component. The mobile phase consisted of 2,6-pyridinedicarboxylic acid as analyte-selective compound, sodium sulfate, and formic acid/sodium formate buffer. Post-column addition of 4-(2-pyridylazo)resorcinol was carried out for spectrophotometric detection of the analytes׳ complexes at 530 nm.Approaches to achieve higher robustness, baseline stability, and detection sensitivity by on-column stacking of the analytes and initial gradient implementation as well as air-cushion pressure damping for post-column reagent addition were studied.The method allowed the rapid separation of copper(II), zinc(II), and iron(II) within 6.5 min including pump refilling and aspiration of sample and 1 mmol HNO3 for analyte stacking on the separation column. High sensitivity was achieved applying an injection volume of up to 90 µL. A signal repeatability of<2% RSD of peak height was found. Analyte recovery evaluated by spiking of different natural water samples was well suited for routine analysis with sub-micromolar limits of detection.

Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Talanta - Volume 136, 1 May 2015, Pages 75–83
نویسندگان
, , , , ,