posted on 2017-03-15, 00:00authored byAdelaide
E. Clark, Subin Yoon, Rebecca J. Sheesley, Sascha Usenko
Atmospheric particulate matter (PM)
samples were collected from
four ground-based sites located in the Houston, TX (September 21–28,
2013) and were analyzed for 12 organophosphate esters (OPEs; current-use
plasticizers and flame retardants). Samples analyzed included daytime,
nighttime, and 24 h PM of <2.5 μm aerodynamic diameter (PM2.5) and total suspended particulate (TSP) samples. PM2.5 and TSP atmospheric ΣOPE concentrations varied over
an order of magnitude and were statistically significantly different
between urban and suburban and industrial sites. Additionally, significant
temporal variability was also identified; for example, daytime atmospheric
concentrations of 2-ethylhexyl diphenyl phosphate (EHDPP; 610 ±
220 pg m–3) measured in TSP samples were significantly
higher than nighttime concentrations (280 ± 180 pg m–3; p = 0.03). Detailed discussions of the spatial
and temporal distribution are given for Tris-(1-chloro-2-propyl) phosphate
(TCiPP), EHDPP, tri-n-butyl phosphate (TnBP), and
triphenyl phosphate (TPhP). Correlations to bulk measurements of carbonaceous
PM including organic carbon, elemental carbon, and water-soluble organic
carbon were used to understand potential sources and urban atmospheric
transport. These results highlight the fundamental complexity associated
with assessing OPE atmospheric concentrations across a large urban
landscape and specific knowledge gaps at the intersection of consumer
products and safety with environmental and human health.