Campo DC | Valor | Idioma |
dc.contributor.author | Portugal, Lindomar Andrade | - |
dc.contributor.author | Laglera, Luis M. | - |
dc.contributor.author | Anthemidis, Aristidis N. | - |
dc.contributor.author | Ferreira, Sergio Luis Costa | - |
dc.contributor.author | Miró, Manuel | - |
dc.creator | Portugal, Lindomar Andrade | - |
dc.creator | Laglera, Luis M. | - |
dc.creator | Anthemidis, Aristidis N. | - |
dc.creator | Ferreira, Sergio Luis Costa | - |
dc.creator | Miró, Manuel | - |
dc.date.accessioned | 2013-10-30T19:06:12Z | - |
dc.date.issued | 2013 | - |
dc.identifier.issn | 0039-9140 | - |
dc.identifier.uri | http://repositorio.ufba.br/ri/handle/ri/13369 | - |
dc.description | p. 58–65 | pt_BR |
dc.description.abstract | A dedicated pressure-driven mesofluidic platform incorporating on-chip sample clean-up and analyte preconcentration is herein reported for expedient determination of trace level concentrations of waterborne inorganic mercury. Capitalizing upon the Lab-on-a-Valve (LOV) concept, the mesofluidic device integrates on-chip micro-solid phase extraction (μSPE) in automatic disposable mode followed by chemical vapor generation and gas–liquid separation prior to in-line atomic fluorescence spectrometric detection. In contrast to prevailing chelating sorbents for Hg(II), bare poly(divinylbenzene-N-vinylpyrrolidone) copolymer sorptive beads were resorted to efficient uptake of Hg(II) in hydrochloric acid milieu (pH=2.3) without the need for metal derivatization nor pH adjustment of prior acidified water samples for preservation to near-neutral conditions. Experimental variables influencing the sorptive uptake and retrieval of target species and the evolvement of elemental mercury within the miniaturized integrated reaction chamber/gas–liquid separator were investigated in detail.
Using merely <10 mg of sorbent, the limits of detection and quantification at the 3sblank and 10sblank levels, respectively, for a sample volume of 3 mL were 12 and 42 ng L−1 Hg(II) with a dynamic range extending up to 5.0 μg L−1. The proposed mesofluidic platform copes with the requirements of regulatory bodies (US-EPA, WHO, EU-Commission) for drinking water quality and surface waters that endorse maximum allowed concentrations of mercury spanning from 0.07 to 6.0 μg L−1. Demonstrated with the analysis of aqueous samples of varying matrix complexity, the LOV approach afforded reliable results with relative recoveries of 86–107% and intermediate precision down to 9% in the renewable μSPE format.
Highlights
► Mesofluidic pressure-driven platform for automatic on-chip μSPE. ► Bead injection in a Lab-on-a-Valve platform for determination of waterborne Hg(II). ► Selective retention of Hg(II) in hydrochloric acid onto bare Oasis HLB® copolymer. ► Determination of Hg(II) at levels below maximum allowed concentrations in waters. | pt_BR |
dc.language.iso | en | pt_BR |
dc.publisher | Talanta | pt_BR |
dc.rights | Acesso Aberto | pt_BR |
dc.source | http://www.sciencedirect.com/science/article/pii/S0039914013000866 | pt_BR |
dc.subject | Lab-on-Valve | pt_BR |
dc.subject | On-chip μSPE | pt_BR |
dc.subject | Automation | pt_BR |
dc.subject | Bead injection | pt_BR |
dc.subject | Inorganic mercury | pt_BR |
dc.subject | Atomic fluorescence spectrometry | pt_BR |
dc.title | Pressure-driven mesofluidic platform integrating automated on-chip renewable micro-solid-phase extraction for ultrasensitive determination of waterborne inorganic mercury | pt_BR |
dc.title.alternative | Talanta | pt_BR |
dc.type | Artigo de Periódico | pt_BR |
dc.description.localpub | Salvador | pt_BR |
dc.identifier.number | v. 110 | pt_BR |
dc.embargo.liftdate | 10000-01-01 | - |
Aparece nas coleções: | Artigo Publicado em Periódico (Química)
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