28 research outputs found

    Preparation, characterisation, and dielectric properties of polypyrrole-clay composites

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    In this study, polypyrrole-clay (PPy-clay) composites were prepared by the in situ chemical oxidative polymerisation of pyrrole in the presence of clay. The chemical structures of the composites were characterised by FTIR and XRD analysis. The thermal properties of these novel composites were analysed by TGA and DSC measurements. Glass-transition temperatures and char yields increased with the increase in clay content in the nanocomposites. The interactions between PPy and clay were mainly between polypyrrole and the layers of clay. It was observed that, as the amount of clay in the composites increased, the dielectric permittivity decreased while the dielectric conductivity of the composite materials increased

    Simultaneous oxidation/co-precipitation of as(Iii) and fe(ii) with hypochlorite and ozone

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    The aim of the study was to investigate oxidative precipitation of As(III) with ozone and sodium hypochlorite in Fe(II) containing water. As guideline value was achieved with both ozone and hypochlorite for 100 µg/l of initial As(III) concentration. High As removal efficiencies were achieved by dosing 2.5 and 5 times the stoichiometric amounts of hypochlorite in the presence of 10 mg/l of initial Fe(II). When the dose of hypochlorite was increased to 10 and 50 times the stoichiometric amount, similar removal efficiencies were achieved with 2.5 and 5 mg/l of initial Fe(II) concentrations. When ozone was dosed at 10 times the stoichiometric amount, 2.5 mg/l of initial Fe(II) presence was sufficient to meet As standard. Simultaneous oxidation and co-precipitation results gave an almost perfect fit to Langmuir isotherm for ozone (r2 ? 0.99). The value of r2 was found as 0.87 for hypochlorite. It was concluded that simultaneous oxidation of As(III) and Fe(II) by ozone and hypochlorite was an effective option to remove low level As(III) from water. As guideline value was not achieved either by ozone or by hypochlorite for high As(III) concentration, even with 10 mg/l of initial Fe(II) existence. Supplemental Fe(II) addition can be taken into consideration to overcome this limitation. © 2016, Scibulcom Ltd. All rights reserved.2012-05-02-KAP05This study was financially supported by the Yildiz Technical University Scientific Research Projects Fund (Research Project Number 2012-05-02-KAP05)

    SIMULTANEOUS OXIDATION/CO-PRECIPITATION OF As(III) AND Fe(II) WITH HYPOCHLORITE AND OZONE

    No full text
    The aim of the study was to investigate oxidative precipitation of As(III) with ozone and sodium hypochlorite in Fe(II) containing water. As guideline value was achieved with both ozone and hypochlorite for 100 mu g/l of initial As(III) concentration. High As removal efficiencies were achieved by dosing 2.5 and 5 times the stoichiometric amounts of hypochlorite in the presence of 10 mg/l of initial Fe(II). When the dose of hypochlorite was increased to 10 and 50 times the stoichiometric amount, similar. removal efficiencies were achieved with 2.5 and 5 mg/l of initial Fe(II) concentrations. When ozone was dosed at 10 times the stoichiometric amount, 2.5 mg/l of initial Fe(II) presence was sufficient to meet As standard. Simultaneous oxidation and co-precipitation results gave an almost perfect fit to Langmuir isotherm for ozone (r(2) approximate to 0.99). The value of r(2) was found as 0.87 for hypochlorite. It was concluded that simultaneous oxidation of As(III) and Fe(II) by ozone and hypochlorite was an effective option to remove low level As(III) from water. As guideline value was not achieved either by ozone or by hypochlorite for high As(III) concentration, even with 10 mg/l of initial Fe(II) existence. Supplemental Fe(II) addition can be taken into consideration to overcome this limitation.Yildiz Technical University Scientific Research Projects FundYildiz Technical University [2012-05-02-KAP05]This study was financially supported by the Yildiz Technical University Scientific Research Projects Fund (Research Project Number 2012-05-02-KAP05)
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