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    Immersed solvent microextraction of phenol and chlorophenols from water samples followed by gas chromatography-mass spectrometry

    , Article Journal of Chromatography A ; Volume 1046, Issue 1-2 , 2004 , Pages 27-33 ; 00219673 (ISSN) Bagheri, H ; Saber, A ; Mousavi, S. R ; Sharif University of Technology
    2004
    Abstract
    A homemade immersed solvent microextraction (SME) device was successfully developed for the trace enrichment of phenols from aqueous samples. A microdrop of butyl acetate was suspended from the tip of a microsyringe needle, immersed in an aqueous spiked solution for a preset time. The microdrop was then retracted into the microsyringe and injected directly into a gas chromatography-mass spectrometry (GC-MS) injection port. Effects of different parameters such as the type of solvent, extraction time, stirring rate, and temperature were investigated and optimized. To reduce the polarity of phenols and prevent tailing effects, all the phenols were derivatized prior to extraction using acetic... 

    Immersed solvent microextraction of aryloxyphenoxypropionate herbicides from aquatic media

    , Article International Journal of Environmental Analytical Chemistry ; Volume 93, Issue 4 , Feb , 2013 , Pages 450-460 ; 03067319 (ISSN) Bagheri, H ; Es'haghi, A ; Es-haghi, A ; Sharif University of Technology
    2013
    Abstract
    An immersed solvent microextraction (SME) method was successfully developed for the trace enrichment of aryloxyphenoxypropionate herbicides from aquatic media. A microdrop of toluene was used as the extraction solvent. Some important extraction parameters such as type of solvent, solvent dropsize, stirring rate, ionic strength and extraction time were investigated and optimized. The microdrop volume of 1.5 μL, a sampling time of 25 min, and use of toluene were major parameters for achieving high enrichment factors. The linearity was studied by preconcentration of 4 mL of the water samples spiked with a standard solution of aryloxyphenoxypropionates at the concentration range of 0.15 to 30 ng... 

    Modified solvent microextraction with back extraction combined with liquid chromatography-fluorescence detection for the determination of citalopram in human plasma

    , Article Analytica Chimica Acta ; Volume 610, Issue 2 , 2008 , Pages 211-216 ; 00032670 (ISSN) Bagheri, H ; Khalilian, F ; Babanezhad, E ; Es haghi, A ; Rouini, M. R ; Sharif University of Technology
    2008
    Abstract
    A modified solvent microextraction with back extraction method (SME/BE) combined with high performance liquid chromatography and fluorescence detection (HPLC-FD) was developed for the determination of citalopram in human plasma. Extraction process was performed in a home-made total glass vial without using a teflon ring, usually employed in SME/BE. Citalopram was first extracted from 0.5 mL of plasma, modified with sodium hydroxide, into hexane. Back extraction step was then performed into 5.2 μL of 45 mM ammonium formate solution (pH 4) using a GC microsyringe. The extract was subsequently transferred into a liner-like vial and then injected into the HPLC system. An enrichment factor of 150... 

    Development of Microextraction Methods
    for the Trace Determination of Organic Compounds in Biological and Environmental Media

    , Ph.D. Dissertation Sharif University of Technology Khalilian, Faezeh (Author) ; Bagheri, Habib (Supervisor)
    Abstract
    The approach of this thesis is to develop and simplify robust microextraction techniques and apply these developed methods to real samples and complex matrices. Firstly, a modified solvent microextraction with back extraction method (SME/BE) combined with high performance liquid chromatography and fluorescence detection (HPLC-FD) was developed for the determination of citalopram in human plasma. Extraction process was performed in a home-made total glass vial without using a teflon ring, usually employed in SME/BE. The evaluation results demonstrated that the calibration curve showed linearity in the range of 1.0–130.0 ng/mL which covers therapeutic window and even lower amounts which is... 

    Preparation and Application of Superhydrophobic Melamine Formaldehyde Modified by Graphene Sorbent for Extraction of Chlorobenzenes from Aqueous Samples by Needle-trap Device

    , M.Sc. Thesis Sharif University of Technology Dorabadi Zare, Farzaneh (Author) ; Bagheri, Habib (Supervisor)
    Abstract
    Superhydrophobic surfaces have attracted much attention in recent years due to their unique properties. Artificial superhydrophobic surfaces can be fabricated by employing chemical modifying a hierarchical structured surface (micro- and nanostructures) with a low surface free energy material. In this report, we used a simple one-step coating process to prepare superhydrophobic sorbents with a large surface area. Surface chemistry and porosity are fundamental parameters for an efficient sorbent capable of extracting low levels of analytes. Considering physical and chemical peroperties of chlorobenzenes, superhydrophobic materials make to be good sorbents. So in this project melamine... 

    Resorcinol-Formaldehyde Xerogel for Analysis of Environmental Pollutant in Aqueous Sample

    , M.Sc. Thesis Sharif University of Technology Zare, Maryam (Author) ; Bagheri, Habib (Supervisor) ; Es-haghi, Ali (Supervisor)
    Abstract
    In this study, a new resorcinol-formaldehyde xerogel was synthesized based on sol-gel technology and employed as a sorbent for micro solid phase extraction (µ-SPE) of BTEX and some selected pesticides from aqueous samples.
    In the first part, a µ-SPE method in combined with headspace solvent microextraction (HS-SME) along with gas chromatography- mass spectrometry detection (GC–MS) was developed for the analysis of BTEX in aqueous samples. In our knowledge, this is for the first time that these two different extraction methods has been coupled to maximize the advantage of each extraction method. Influential parameters such as the peristaltic pump flow rate, extraction volume, extraction... 

    Multivariate optimization of hydrodistillation-headspace solvent microextraction of thymol and carvacrol from Thymus transcaspicus

    , Article Talanta ; Volume 79, Issue 3 , 2009 , Pages 695-699 ; 00399140 (ISSN) Kiyanpour, V ; Fakhari, A. R ; Alizadeh, R ; Asghari, B ; Jalali Heravi, M ; Sharif University of Technology
    2009
    Abstract
    In this paper multivariate response surface methodology (RSM) has been used for the optimization of hydrodistillation-headspace solvent microextraction (HD-HSME) of thymol and carvacrol in Thymus transcaspicus. Quantitative determination of compounds of interest was performed simultaneously using gas chromatography coupled with flame ionization detector (GC-FID). Parameters affecting the extraction efficiency were assessed and the optimized values were 5 min, 2 μL and 3 min for the extraction time, micro-drop volume and cooling time after extraction, respectively. The amounts of analyte extracted increased with plant weight. The calibration curves were linear in the ranges of 6.25-81.25 and... 

    Immersed solvent microextraction and gas chromatography-mass spectrometric detection of s-triazine herbicides in aquatic media

    , Article Analytica Chimica Acta ; Volume 537, Issue 1-2 , 2005 , Pages 81-87 ; 00032670 (ISSN) Bagheri, H ; Khalilian, F ; Sharif University of Technology
    Elsevier  2005
    Abstract
    An immersed solvent microextraction (SME) method was successfully developed for the trace enrichment of s-triazine herbicides from aquatic media. A microdrop of butyl acetate was applied as the extraction solvent. After extraction, the microdrop was introduced directly into a gas chromatography-mass spectrometry (GC-MS) injection port. Some important extraction parameters such as type of solvent, extraction time, stirring rate, and temperature were investigated and optimized. The highest possible microdrop volume of 3 μl, a sampling temperature of 60°C, and use of butyl acetate are major parameters to obtain high enrichment factors. The enrichment factor and linearity was studied by...