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      Synthesis of Nano-Pore Size Ag(I)-Imprinted Polymer for the Extraction and Preconcentration of Silver Ions Followed by Its Determination with Flame Atomic Absorption Spectrometry and Spectrophotometry Using Localized Surface Plasmon Resonance Peak of Silver Nanoparticles

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          Abstract

          Silver ion imprinted polymer (IIP) was synthesized in the presence of Ag(I)-N,N’‑bis(salicylidene)ethylenediamine (salen) complex using 4-vinylpyridine as the functional monomer, ethylene glycol dimethacrylate (EGDMA) as the crosslinker, and 2,2-azobis(isobutyronitrile) (AIBN) as the initiator. The Ag(I)-imprinted polymer (IIP) particles were characterized by SEM (scanning electron microscope), FTIR (Fourier transform infrared spectroscopy) and BET/BJH (Brunauer-Emmett-Teller/Barrett-Joyner-Halenda) analysis. The imprinted Ag(I) ions were completely removed by leaching the IIP with thiourea (0.5 mol L-1). The polymer was employed as a selective sorbent for extraction and separation of the trace amounts of the Ag(I) ions. The preconcentrated ion was determined via the flame atomic absorption spectrometry (FAAS) or it was reduced to silver nanoparticles and quantified by spectrophotometry based on its localized surface plasmon resonance peak (LSPRP). The figures of merit of both methods were compared. Under the optimized conditions, a sample volume of 80 mL resulted in an enhancement factor of 312. The detection limit (3Sb/m) and the relative standard deviation (n = 10) at 10 µg L-1 level for FAAS were found to be 0.06 µg L-1, 2.9%, whereas for the LSPRP method they were 0.5 µg L-1 and 10.3%, respectively. The methods were successfully applied to the determination of silver in radiology film, hair, nails, and water samples.

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          Origins of regioselectivity of the palladium-catalyzed (aromatic)CH bond metalation–deprotonation

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            O2 activation by nonheme iron complexes: A monomeric Fe(III)-Oxo complex derived from O2.

            Iron species with terminal oxo ligands are implicated as key intermediates in several synthetic and biochemical catalytic cycles. However, there is a dearth of structural information regarding these types of complexes because their instability has precluded isolation under ambient conditions. The isolation and structural characterization of an iron(III) complex with a terminal oxo ligand, derived directly from dioxygen (O2), is reported. A stable structure resulted from placing the oxoiron unit within a synthetic cavity lined with hydrogen-bonding groups. The cavity creates a microenvironment around the iron center that aids in regulating O2 activation and stabilizing the oxoiron unit. These cavities share properties with the active sites of metalloproteins, where function is correlated strongly with site structure.
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              Chem. Rev.

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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Journal
                jbchs
                Journal of the Brazilian Chemical Society
                J. Braz. Chem. Soc.
                Sociedade Brasileira de Química (São Paulo )
                1678-4790
                June 2015
                : 26
                : 6
                : 1180-1190
                Affiliations
                [1 ] Yazd University Iran
                Article
                S0103-50532015000601180
                10.5935/0103-5053.20150082
                727c1bba-5376-4625-ad3d-f0684cab8399

                http://creativecommons.org/licenses/by/4.0/

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                SciELO Brazil

                Self URI (journal page): http://www.scielo.br/scielo.php?script=sci_serial&pid=0103-5053&lng=en
                Categories
                CHEMISTRY, MULTIDISCIPLINARY

                General chemistry
                silver nanoparticles,localized surface plasmon resonance peak,flame atomic absorption spectrometry,silver,solid phase extraction,ion imprinted polymer

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