Comparisons of indoor active and passive air sampling methods for emerging and legacy halogenated flame retardants in Beijing, China offices

One active and two passive air sampling configurations were deployed simultaneously in three offices in Beijing,China to test their comparability for sampling emerging and legacy halogenated flame retardants spanning a large range of octanoleair partition coefficients(KOA).Sampling in each office was carried out for three consecutive 28-day periods in the spring-summer of 2013.The active sampler was run for 2.5 h at different times every day for 28 days to parallel the passive samplers and sample a total volume comparable to that sampled by the passive samplers(~20 m^3).At the end of each 28-day sampling period,a separate active air sample was taken by running the sampler pump continuously for about 2.5 days.The comparability of measured concentrations varied between the air sampling configurations and for different compounds.The predominant compound measured in nearly all samples was BDE-209,a compound known to have heavy use in China.Several emerging flame retardants were also detected including DBE-DBCH,PBT,HBB,DDC-CO,and DBDPE.Very little of the tetra-hexabrominated BDEs associated with the technical PentaBDE product was observed.

Sources and Trends of Persistent Organic Pollutants at Three Passive Monitoring Sites in South Africa

The Stockholm Convention on Persistent Organic Pollutants (SCPOPs) is an international treaty that operates under the patronage of the United Nations (UN) to control certain chemicals that are considered persistent organic pollutants (POPs). They are of great concern because of their adverse effects on human health and the environment. Exposure to POPs may lead to cancer, infertility, respiratory infections, and other health complications. It is therefore critical to study the degree of human and environmental exposure to these POPs. Passive air sampling was conducted in South Africa to evaluate the presence and trends of persistent organic pollutants at Barberspan (rural agricultural), Vanderbijl Park (urban industrial) and Molopo Nature Reserve (isolated nature reserve). Samples were collected in 2012. Passive air samplers using poly were used for sampling. The Buchi System B-811 automatic extractor was used to analyze for dichloro-diphenyl-trichlorethane (DDT), pentachlorobenzene (PeCB), hexechlorobenzene (HCB) polychlorinated biphenyls (PCBs) and hexachlorocyclohexane (HCH). Sampling was conducted for a period of one year. POPs concentrations were generally low at all sites, but Vanderbijl Park had the highest concentrations. Seasonal changes in concentrations were much the same at the three sites with temperatures and wind patterns being major factors. The presence of these chemicals in Molopo Nature Reserve and Barberspan is evidence of long range transportation over dry semi desert areas. Back-trajectories indicate possible sources, including areas where DDT is used for malaria control. The presence of POPs is areas they have never been in use poses health and environmental risks in these areas.

Levels and Sources of Atmospheric Polycyclic Aromatic Hydrocarbons Surrounding an Oil Refinery in Curacao

This research measured ambient levels of polycyclic aromatic hydrocarbons (PAHs) surrounding a petrochemical complex on the island of Curacao using passive air sampling. In addition, source elucidation of PAHs was conducted using concentration profiles, distribution profiles, binary diagnostic ratios and factor analysis. Passive air samplers with polyurethane foam collection disks (PAS-PUFs) were deployed in 2011 (n = 43) and in 2014 (n = 30) to evaluate the extent of the emission plume as well as spatial and temporal differences in ambient PAH concentrations. In general, ambient PAH concentrations in Curacao were consistent with other urban and industrialized regions of the world;however, the levels measured downwind of Isla Refineriá petrochemical complex were among some of the highest reported ambient PAHs globally. Ambient PAH concentrations ranged from 1.2 to 790 ng/m3 in 2011 and 27 to 660 ng/m3 in 2014, demonstrating no temporal differences. However, significant spatial differences were detected between samples collected upwind and downwind of the petrochemical complex. Significantly higher ambient PAH concentrations were found in the samples collected downwind of the petrochemical complex compared to those upwind in 2014