کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1234278 1495244 2014 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Development of on-line spectroscopic determination approach of dispersive liquid–liquid microextraction based on an effective device
ترجمه فارسی عنوان
توسعه روش خطی طیفی تشخیصی مایع مایکروکساکتیو مایع منی بر اساس یک دستگاه موثر
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
چکیده انگلیسی


• An on-line determination method of DLLME was developed based on an effective device.
• The volume of sample can conveniently change to perform a more effective DLLME.
• The proposed device provided a repeatable and effective injection of the extractant.
• The method was used to quantify a model analyte rhodamine B in three real samples.
• The applicability of the method can be extended to other analytes.

A novel, rapid, simple, and low-cost on-line determination approach of dispersive liquid–liquid microextraction (DLLME) with low-density solvents was developed with the support of a specially designed effective homemade device. The proposed method surmounted the drawbacks of conventional DLLME of the need of high-density solvents as extractants, and the requirement of centrifugation operation to obtain phase separation, and the difficulties to realize on-line determination. The amount of sample utilized can conveniently change according to practical needs by varying the volume of the extraction tube of the device to perform a more effective DLLME. A case study was carried out to assess this method utilizing the dye rhodamine B as the model analyte. The experiment parameters influencing the extraction were systematically investigated. Under optimum conditions, the linearity was obtained in the range of 0.015–1.000 μg/mL with the correlation coefficient (r2) of 0.9980. The limit of detection and quantification were 6.1 and 20.4 μg/L, respectively. Good repeatability was achieved with the relative standard deviations (RSD) for five replicate measurements of different concentration samples less than 4.06%, and the presented method was successfully employed to quantify rhodamine B in three real samples.

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy - Volume 124, 24 April 2014, Pages 159–164
نویسندگان
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