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1.
Anal Bioanal Chem ; 408(19): 5137-45, 2016 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-26960902

RESUMEN

Nanoparticles (NPs) entering water systems are an emerging concern as NPs are more frequently manufactured and used. Single particle inductively coupled plasma-mass spectrometry (SP-ICP-MS) methods were validated to detect Zn- and Ce-containing NPs in surface and drinking water using a short dwell time of 0.1 ms or lower, ensuring precision in single particle detection while eliminating the need for sample preparation. Using this technique, information regarding NP size, size distribution, particle concentration, and dissolved ion concentrations was obtained simultaneously. The fates of Zn- and Ce-NPs, including those found in river water and added engineered NPs, were evaluated by simulating a typical drinking water treatment process. Lime softening, alum coagulation, powdered activated carbon sorption, and disinfection by free chlorine were simulated sequentially using river water. Lime softening removed 38-53 % of Zn-containing and ZnO NPs and >99 % of Ce-containing and CeO2 NPs. Zn-containing and ZnO NP removal increased to 61-74 % and 77-79 % after alum coagulation and disinfection, respectively. Source and drinking water samples were collected from three large drinking water treatment facilities and analyzed for Zn- and Ce-containing NPs. Each facility had these types of NPs present. In all cases, particle concentrations were reduced by a minimum of 60 % and most were reduced by >95 % from source water to finished drinking water. This study concludes that uncoated ZnO and CeO2 NPs may be effectively removed by conventional drinking water treatments including lime softening and alum coagulation.


Asunto(s)
Cerio/análisis , Agua Potable/química , Nanopartículas del Metal/análisis , Espectrofotometría Atómica/métodos , Contaminantes Químicos del Agua/análisis , Purificación del Agua/métodos , Óxido de Zinc/análisis , Agua Potable/análisis , Reproducibilidad de los Resultados , Sensibilidad y Especificidad
2.
Chemosphere ; 144: 148-53, 2016 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-26347937

RESUMEN

One of the most direct means for human exposure to nanoparticles (NPs) released into the environment is drinking water. Therefore, it is critical to understand the occurrence and fate of NPs in drinking water systems. The objectives of this study were to develop rapid and reliable analytical methods and apply them to investigate the fate and transportation of NPs during drinking water treatments. Rapid single particle ICP-MS (SP-ICP-MS) methods were developed to characterize and quantify titanium-containing, titanium dioxide, silver, and gold NP concentration, size, size distribution, and dissolved metal element concentration in surface water and treated drinking water. The effectiveness of conventional drinking water treatments (including lime softening, alum coagulation, filtration, and disinfection) to remove NPs from surface water was evaluated using six-gang stirrer jar test simulations. The selected NPs were nearly completely (97 ± 3%) removed after lime softening and alum coagulation/activated carbon adsorption treatments. Additionally, source and drinking waters from three large drinking water treatment facilities utilizing similar treatments with the simulation test were collected and analyzed by the SP-ICP-MS methods. Ti-containing particles and dissolved Ti were present in the river water samples, but Ag and Au were not present. Treatments used at each drinking water treatment facility effectively removed over 93% of the Ti-containing particles and dissolved Ti from the source water.


Asunto(s)
Oro/análisis , Nanopartículas del Metal/análisis , Plata/análisis , Titanio/análisis , Contaminantes Químicos del Agua/análisis , Purificación del Agua/métodos , Adsorción , Compuestos de Alumbre/química , Compuestos de Calcio/química , Carbono/química , Desinfección , Agua Potable/análisis , Filtración , Floculación , Espectrometría de Masas/métodos , Óxidos/química , Ríos/química , Ablandamiento del Agua
3.
Environ Sci Pollut Res Int ; 17(7): 1323-30, 2010 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-20309737

RESUMEN

BACKGROUND, AIMS, AND SCOPE: Heavy metal contaminants in environment, especially in drinking water, are always of great concern due to their health impact. Due to the use of heavy metals as catalysts during plastic syntheses, particularly antimony, human exposure to metal release from plastic bottles has been a serious concern in recent years. The aim and scope of this study were to assess metal contaminations leaching out from a series of recycling plastic bottles upon treatments. METHODOLOGY: In this study, leaching concentrations of 16 metal elements were determined in 21 different types of plastic bottles from five commercial brands, which were made of recycling materials ranging from no. 1 to no. 7. Several sets of experiments were conducted to study the factors that could potentially affect the metal elements leaching from plastic bottles, which include cooling with frozen water, heating with boiling water, microwave, incubating with low-pH water, outdoor sunlight irradiation, and in-car storage. RESULTS: Heating and microwave can lead to a noticeable increase of antimony leaching relative to the controls in bottle samples A to G, and some even reached to a higher level than the maximum contamination level (MCL) of the US Environmental Protection Agency (USEPA) regulations. Incubation with low-pH water, outdoor sunlight irradiation, and in-car storage had no significant effect on antimony leaching relative to controls in bottle samples A to G, and the levels of antimony leaching detected were below 6 ppb which is the MCL of USEPA regulations. Cooling had almost no effect on antimony leaching based on our results. For the other interested 15 metal elements (Al, V, Cr, Mn, Co, Ni, Cu, As, Se, Mo, Ag, Cd, Ba, Tl, Pb), no significant leaching was detected or the level was far below the MCL of USEPA regulations in all bottle samples in this study. In addition, washing procedure did contribute to the antimony leaching concentration for polyethylene terephthalate (PET) bottles. The difference of antimony leaching concentration between washing procedure involved and no washing procedure involved (AC) was larger than zero for samples A to G. This interesting result showed that higher antimony concentration was detected in experiments with no washing procedures compared with those experiments with washing procedures. Our study results indicate that partial antimony leaching from PET bottles comes from contaminations on the surface of plastic during manufacturing process, while major antimony leaching comes from conditional changes. CONCLUSION: The results revealed that heating and microwaving enhance antimony leaching significantly in PET plastic bottles. Plastic bottle manufacturers should consider the contaminations during manufacturing process and washing bottles before first use was strongly recommended to remove those contaminants.


Asunto(s)
Conservación de los Recursos Naturales/métodos , Embalaje de Alimentos , Metales/análisis , Plásticos/química , Eliminación de Residuos/métodos , Agua/química , Antimonio/análisis , Arsénico/análisis , Frío/efectos adversos , Contaminación de Alimentos/prevención & control , Calor/efectos adversos , Concentración de Iones de Hidrógeno , Microondas/efectos adversos , Plásticos/efectos de la radiación , Tereftalatos Polietilenos/química , Tereftalatos Polietilenos/efectos de la radiación , Polímeros/química , Polímeros/efectos de la radiación , Selenio/análisis , Luz Solar/efectos adversos
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