Speciation and detection of arsenic in aqueous samples: A review of recent progress in non-atomic spectrometric methods |
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Authors: | Jian Ma Mrinal K. Sengupta Dongxing Yuan Purnendu K. Dasgupta |
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Affiliation: | 1. State Key Laboratory of Marine Environmental Science, College of the Environment and Ecology, Xiamen University, Xiamen 361102, China;2. Department of Chemistry and Biochemistry, University of Texas, 700 Planetarium Place, Arlington, TX 76019, United States;3. Thermo Fisher Scientific, Dionex Products, 445 Lakeside Drive, Sunnyvale, CA, 94085, United States |
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Abstract: | Inorganic arsenic (As) displays extreme toxicity and is a class A human carcinogen. It is of interest to both analytical chemists and environmental scientists. Facile and sensitive determination of As and knowledge of the speciation of forms of As in aqueous samples are vitally important. Nearly every nation has relevant official regulations on permissible limits of drinking water As content. The size of the literature on As is therefore formidable. The heart of this review consists of two tables: one is a compilation of principal official documents and major review articles, including the toxicology and chemistry of As. This includes comprehensive official compendia on As speciation, sample treatment, recommended procedures for the determination of As in specific sample matrices with specific analytical instrument(s), procedures for multi-element (including As) speciation and analysis, and prior comprehensive reviews on arsenic analysis. The second table focuses on the recent literature (2005–2013, the coverage for 2013 is incomplete) on As measurement in aqueous matrices. Recent As speciation and analysis methods based on spectrometric and electrochemical methods, inductively coupled plasma-mass spectrometry, neutron activation analysis and biosensors are summarized. We have deliberately excluded atomic optical spectrometric techniques (atomic absorption, atomic fluorescence, inductively coupled plasma-optical emission spectrometry) not because they are not important (in fact the majority of arsenic determinations are possibly carried out by one of these techniques) but because these methods are sufficiently mature and little meaningful innovation has been made beyond what is in the officially prescribed compendia (which are included) and recent reviews are available. |
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Keywords: | AAPTS, N-(2-aminoethyl)-3-aminopropyltrimethoxysilane AES, atomic emission spectrometry APDC, ammonium pyrrolidine dithiocarbamate ASV, anodic stripping voltammetry ATR-FTIR, attenuated total reflectance Fourier transform infrared spectroscopy AuNP, gold nanoparticle BGE, background electrolyte CCD, charge-coupled device CE, capillary electrophoresis CME, capillary microextraction CNFs, carbon nanofibers CRM, certified reference material CSV, cathodic stripping voltammetry CTAB, cetyltimethylammonium bromide DGT, diffusive gradients in thin films DMA, dimethylarsinic acid DS, diffusion scrubber DTT, dithiothreitol ETV, electrothermal vaporization FI, flow injection GCE, glassy carbon electrode GFAAS, graphite furnace atomic absorption GPCL, Gas phase chemiluminescence GSH, glutathione HG, hydride generation HGAAS, hydride generation atomic absorption spectrometry HGAFS, hydride generation atomic fluorescence spectrometry HPLC, high performance liquid chromatography IC, ion chromatography ICP-MS, inductively coupled plasma-mass spectrometry LIBS, laser-induced breakdown spectroscopy LLME, liquid&ndash liquid microextraction LOD, limit of detection LPCL, liquid phase chemiluminescence LSV, linear sweep voltammetry MA, mercaptoacetic acid MB, molybdenum blue MCL, maximum contaminant level MDL, method detection limit MMA, monomethylarsonic acid MPTS, mercaptopropyltrimethoxysilane NAA, neutron activation analysis NaDBC, sodium dibenzyldithiocarbamate PMT, photomultiplier tube PTFE, polytetrafluoroethylene QDs, quantum dots RTIL, room temperature ionic liquid SAM, self-assembled monolayer SBSE, solvent bar microextraction SERS, surface-enhanced Raman spectroscopy SPE, solid phase extraction SPME, solid phase microextraction SPR, surface plasmon resonance SWASV, square wave anodic stripping voltammetry SWNTs, single-wall carbon nanotubes TMAO, trimethylarsine oxide TXRF, total reflection X-ray fluorescence spectrometry USEPA, United States Environmental Protection Agency UV, ultra violet VMoAs-HPA, vanadomolybdoarsenic heteropoly acid WHO, World Health Organization |
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