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1.
Environ Sci Process Impacts ; 25(9): 1491-1504, 2023 Sep 20.
Artículo en Inglés | MEDLINE | ID: mdl-37584085

RESUMEN

Exposures to metals from industrial emissions can pose important health risks. The Chester-Trainer-Marcus Hook area of southeastern Pennsylvania is home to multiple petrochemical plants, a refinery, and a waste incinerator, most abutting socio-economically disadvantaged residential communities. Existing information on fenceline community exposures is based on monitoring data with low temporal and spatial resolution and EPA models that incorporate industry self-reporting. During a 3 week sampling campaign in September 2021, size-resolved particulate matter (PM) metals concentrations were obtained at a fixed site in Chester and on-line mobile aerosol measurements were conducted around Chester-Trainer-Marcus Hook. Fixed-site arsenic, lead, antimony, cobalt, and manganese concentrations in total PM were higher (p < 0.001) than EPA model estimates, and arsenic, lead, and cadmium were predominantly observed in fine PM (<2.5 µm), the PM fraction which can penetrate deeply into the lungs. Hazard index analysis suggests adverse effects are not expected from exposures at the observed levels; however, additional chemical exposures, PM size fraction, and non-chemical stressors should be considered in future studies for accurate assessment of risk. Fixed-site MOUDI and nearby mobile aerosol measurements were moderately correlated (r ≥ 0.5) for aluminum, potassium and selenium. Source apportionment analyses suggested the presence of four major emissions sources (sea salt, mineral dust, general combustion, and non-exhaust vehicle emissions) in the study area. Elevated levels of combustion-related elements of health concern (e.g., arsenic, cadmium, antimony, and vanadium) were observed near the waste incinerator and other industrial facilities by mobile monitoring, as well as in residential-zoned areas in Chester. These results suggest potential co-exposures to harmful atmospheric metal/metalloids in communities surrounding the Chester-Trainer-Marcus Hook industrial area at levels that may exceed previous estimates from EPA modeling.


Asunto(s)
Contaminantes Atmosféricos , Contaminación del Aire , Arsénico , Metales Pesados , Selenio , Contaminantes Atmosféricos/análisis , Contaminación del Aire/análisis , Monitoreo del Ambiente/métodos , Antimonio/análisis , Arsénico/análisis , Cadmio/análisis , Material Particulado/análisis , Polvo/análisis , Selenio/análisis , Vanadio/análisis , Aerosoles/análisis , Metalurgia , Metales Pesados/análisis
2.
J Hazard Mater ; 376: 178-187, 2019 08 15.
Artículo en Inglés | MEDLINE | ID: mdl-31128397

RESUMEN

We have synthesized iron oxide doped carbon nitride with 0.5 to 2 wt.% iron oxide and characterized by XPS, TGA, FTIR, SEM, photoluminescence spectroscopy and photoelectrochemical measurements. A herbicide, dicamba was employed as model organic pollutant for degradation in presence with the catalyst and hydrogen peroxide. A 3D printed photon concentrator with two chips on board (COB) LEDs with visible light spectra and two complex parabolic mirror surfaces was used as photo-reactor. The findings revealed that both photocurrent and degradation of dicamba were functions of light intensity and concentrator geometry. The rapid degradation of dicamba can be attributed to the holistic and individual actions of structural components of the photocatalyst. Four distinct phenomena, including photocatalytic activity of carbon nitride, quenching of electron/hole pairs and generation of additional reactive hydroxyl radicals by hydrogen peroxide, Fenton and photo-Fenton activity of iron oxide component of carbon nitride in presence of hydrogen peroxide and photocatalytic activity of iron oxide alone in conjuncture with carbon nitride can contribute to the overall photocatalytic activity of the system. Liquid Chromatography-Mass spectrometry (LCMS) analysis of the degradation products showed loss of chlorine from the aromatic ring and evidence of free radical addition reactions in the course of photocatalysis.

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