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41.
Mahnaz?Nozohour Yazdi Yadollah?YaminiEmail author Hamid?Asiabi Abdolali?Alizadeh 《Mikrochimica acta》2018,185(11):525
Novel composites were obtained via direct assembly of polysulfides (Sx2?, X?=?3, 4, 6) on the surface of a metal organic framework (MOF; type benzene-1,3,5-tricarboxylic/Cu(II). They are referred to as Sx-MOFs and were used for highly selective and efficient extraction of ultra-trace amounts of heavy metal ions from aqueous solutions. The structure of the Sx-MOFs was characterized by Raman spectroscopy, FT-IR, X-ray diffraction, and scanning electron microscopy. The Raman spectra of Sx-MOF is similar to the bare MOF and shows the MOFs structure to be well retained after Sx functionalization. The selective interaction of Sx with soft metal ions and the high surface area of MOFs resulted in excellent affinity and selectivity for ions such as Hg(II). The Sx-MOFs of type S4-MOF had the highest distribution coefficient Kd value (~107) and best extraction recovery (~100%) for Hg(II). The S4-MOF also has high selectivity in the following order: Hg(II) >?>?Pb(II)?>?Zn(II)?>?Ni(II)?>?Co(II). The binding process of the metals occurs via M–S bonding. The ions were quantified by inductively coupled plasma optical emission spectrometry (ICP-OES). The detection limit for Hg(II) is 0.13 μg L?1. The S4-MOF was applied to the extraction of trace metal ions from natural and contaminated waters and data were compared with other sorbets. The results revealed that S4-MOF is an excellent adsorbent for sorption of heavy metal ions even in the presence of the relatively high concentration of other ions. 相似文献
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Haniye Dehestani Yadollah Ordokhani Mohsen Razzaghi 《Mathematical Methods in the Applied Sciences》2019,42(18):7296-7313
In this paper, we present a novel discrete scheme based on Genocchi polynomials and fractional Laguerre functions to solve multiterm variable‐order time‐fractional partial differential equations (M‐V‐TFPDEs) in the large interval. In this purpose, the accurate modified operational matrices are constructed to reduce the problems into a system of algebraic equations. Also, the computational algorithm based on the method and modified operational matrices in the large interval is easily implemented. Furthermore, we discuss the error estimation of the proposed method. Ultimately, to confirm our theoretical analysis and accuracy of numerical approach, several examples are presented. 相似文献
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The investigation of flower scent represents an important field of modern biological research which is directed towards special theories of biological recognition. The headspace solid phase microextraction coupled with gas chromatography-mass spectrometry was used to identify the volatile components of Carum copticum (C. copticum) cultivated in Iran. The compounds were identified according to their retention indices and mass spectra (EI, 70 eV). The effects of different parameters, such as the desorption time, the extraction temperature, the sample mass, the addition of salt, the pre-equilibration time and the extraction time, on the extraction efficiency were investigated. The optimized conditions were: the desorption time, 2 min; the extraction temperature, 58 degrees Celsius; the sample mass, 1.000 g in 4.0 mL 2.0 M NaCl solution; the pre-equilibration time, 25 min; the extraction time, 20 min. Finally, ten components were identified in the volatile components of C. copticum. The major components of C. copticum were thymol (68.2%), gamma-terpinene (13.9%), p-cymene (11.6%), myrcene (1.0%) and beta-pinene (0.6%). Precision of the proposed method is good and %RSD less than 14 was obtained. 相似文献
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Mohsenzadeh Farshid Darabi Hossein Reza Alivand Mahsa Aghapoor Kioumars Balavar Yadollah 《Research on Chemical Intermediates》2020,46(12):5255-5262
Research on Chemical Intermediates - In this study, common naturally occurring organic acids, namely oxalic, malonic, succinic, tartaric and citric acid (as safe, inexpensive, and biodegradable... 相似文献
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Electromembrane extraction coupled with high-performance liquid chromatography (HPLC) and ultraviolet (UV) detection was developed for the determination of levamisole in some human biological fluids. Levamisole migrated from 4 mL of different acidized biological matrices, through a thin layer of 2-nitrophenyl octyl ether containing 5% tris-(2-ethylhexyl) phosphate immobilized in the pores of a porous hollow fiber, into a 20-μL acidic aqueous acceptor solution present inside the lumen of the fiber. The parameters influencing electromigration were investigated and optimized. Within 15 min of operation at 200 V, levamisole was extracted from different biological fluid samples with recoveries in the range of 59-65%, which corresponded to preconcentration factors in the range of 118-130. The calibration curves showed linearity in the range of 0.5-10, 0.2-10 and 0.1-10 μg/mL for plasma, urine and saliva, respectively. Limits of detection of 0.1, 0.07 and 0.05 μg/mL and limits of quantification of 0.5, 0.2 and 0.1 μg/mL were obtained for plasma, urine and saliva, respectively. The relative standard deviations of the analysis were found to be in the range of 5.6-9.7% (n = 3). Electromembrane extraction was successfully processed for determination of levamisole in plasma, urine and saliva samples. 相似文献
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Mohammad Rezaee Yadollah Yamini Hossein Ali Mashayekhi Mohammad Hosein Naeeni Mostafa Bashiri Jubari 《中国化学会会志》2011,58(3):332-339
In this study, simple and efficient ultrasound‐assisted dispersive liquid‐liquid microextraction combined with gas chromatography (GC) was developed for the preconcentration and determination of methyl‐tert‐butyl ether (MTBE) in water samples. One hundred microliters of benzyl alcohol was injected slowly into 10 mL home‐designed centrifuge glass vial containing an aqueous sample with 30% (w/v) of NaCl that was located inside the ultrasonic water bath. The formed emulsion was centrifuged and 2 μL of separated benzyl alcohol was injected into a gas chromatographic system equipped with a flame ionization detector (GC‐FID) for analysis. Several factors influencing the extraction efficiency such as the nature and volume of organic solvent, extraction temperature, ionic strength and centrifugation times were investigated and optimized. Using optimum extraction conditions a detection limit of 0.05 μg L‐1 and a good linearity (r2 = 0.998) in a calibration range of 0.1‐500 μg L‐1 were achieved. This proposed method was successfully applied to the analysis of MTBE in tap, well and a ground water sam ple contaminated by leaking gasoline from an underground storage tank (LUST) in a gasoline service station. 相似文献
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Homeira Ebrahimzadeh Ali Mehdinia Yadollah Yamini Saeed Kasraee Amir Gholizade 《International journal of environmental analytical chemistry》2013,93(13):963-975
Nano-structured polypyrrole (PPY) was used as a coating of solid-phase microextraction (SPME) fibre to increase the extraction efficiency of headspace solid phase microextraction (HS-SPME) of mono-nitrotoluene (MNT) isomers in water samples. The nano-structured PPY was prepared electrochemically by template-free method in the presence of dodecylbenzene sulphonate (DBS) as dopant. Nano-fibrous structures of PPY with a diameter in the range of 38–129 nm were obtained. The porous surface structure of the film, revealed by scanning electron microscopy (SEM), provided high surface areas and allowed for high extraction efficiency of MNT isomers. The extraction procedure was optimised by selecting the appropriate extraction parameters including the time and temperature of adsorption, salt concentration and stirring rate. The calibration graphs obtained by HS-SPME using the proposed fibre followed by GC-FID analysis were linear in a concentration range of 0.1–500 µg L?1 (r > 0.999) with detection limits below 0.012 µg L?1 for three isomers. Repeatability of the method was less than 6% (RSD%, n = 4). Good recoveries (88–108%) were obtained for the extraction of mono-nitrotoluenes in real water samples. 相似文献
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Hamid Asiabi Yadollah Yamini Maryam Shamsayei Tahmine Baheri 《Journal of separation science》2020,43(6):1128-1136
A novel plate‐like nano‐sorbent based on copper/cobalt/chromium layered double hydroxide was synthesized by a simple coprecipitation method. The synthesized nanoparticels were introduced into a stainless steel cartridge using a dry packing method. Then, the packed cartridge was introduced as a novel on‐line “packed in‐tube” configuration and followed by high performance liquid chromatography for the determination of trace amounts of ?9‐tetrahydrocannabinol from biological samples and cannabis leaves. The as‐prepared sorbent exhibited long lifetime, good chemical stability, and high anion‐exchange capacity. Several important factors affecting the extraction efficiency, such as extraction and desorption times, pH of the sample solution and flow rates of the sample and eluent solutions, were investigated and optimized. Under optimized conditions, this method showed good linearity for ?9‐tetrahydrocannabinol in the ranges of 0.09–500, 0.3–500, and 0.4–500 µg/L with coefficients of determination of 0.9999, 0.9991, and 0.9994 in water, serum and plasma samples, respectively. The inter‐ and intra‐assay precisions (n = 3) were respectively in the ranges of 1.8–4.6% and 1.9–4.0% at three concentration levels of 10, 50, and 100 µg/L. The limits of detection were also in the range of 0.02–0.1 µg/L. 相似文献