Yuso Kobara

Contamination of indoor dust and air by polychlorinated biphenyls and brominated flame retardants and relevance of non-dietary exposure in Vietnamese informal e-waste recycling sites

This study investigated the occurrence of polychlorinated biphenyls (PCBs), and several additive brominated flame retardants (BFRs) in indoor dust and air from two Vietnamese informal e-waste recycling sites (EWRSs) and an urban site in order to assess the relevance of these media for human exposure. The levels of polybrominated diphenyl ethers (PBDEs), hexabromocyclododecane (HBCD), 1,2-bis-(2,4,6-tribromophenoxy)ethane (BTBPE) and decabromodiphenyl ethane (DBDPE) in settled house dust from the EWRSs (130-12,000, 5.4-400, 5.2-620 and 31-1400 ng g(-1), respectively) were significantly higher than in urban house dust but the levels of PCBs (4.8-320 ng g(-1)) were not higher. The levels of PCBs and PBDEs in air at e-waste recycling houses (1000-1800 and 620-720 pg m(-3), respectively), determined using passive sampling, were also higher compared with non-e-waste houses. The composition of BFRs in EWRS samples suggests the influence from high-temperature processes and occurrence of waste materials containing older BFR formulations. Results of daily intake estimation for e-waste recycling workers are in good agreement with the accumulation patterns previously observed in human milk and indicate that dust ingestion contributes a large portion of the PBDE intake (60%-88%), and air inhalation to the low-chlorinated PCB intake (>80% for triCBs) due to their high levels in dust and air, respectively. Further investigation of both indoor dust and air as the exposure media for other e-waste recycling-related contaminants and assessment of health risk associated with exposure to these contaminant mixtures is necessary.

Passive air monitoring of PCBs and PCNs across East Asia: A comprehensive congener evaluation for source characterization

A comprehensive congener specific evaluation of polychlorinated biphenyls (PCBs) and polychlorinated naphthalenes (PCNs) in the atmosphere was conducted across East Asia in spring 2008, applying polyurethane foam (PUF) disk passive air sampler (PAS) as monitoring device. Mean concentrations derived for Japan, China and Korea were 184 ± 24, 1100 ± 118, and 156 ± 20 pg m(-3) for ∑(202) PCBs, and 9.5 ± 1.5, 61 ± 6, and 16 ± 2.4 pg m(-3) for ∑(63) PCNs, respectively. Relative to reported data from 2004, the present results suggest that air PCBs concentrations have not changed much in Japan and Korea, while it has increased by one order of magnitude in China. From principal component analysis, combustion emerged highly culpable in contemporary emissions of both PCBs and PCNs across the East Asian sub-region. Another factor derived as important to air PCBs was re-emissions/volatilization. Signals from PCBs formulations were also picked, but their general importance was virtually consigned to the re-emissions/volatilization tendencies. On the contrary, counterpart PCNs formulations did not appear to contribute much to air PCNs.

Perfluorinated Compounds in the Asian Atmosphere

There is interest in the production, use, and environmental occurrence of perfluorinated compounds (PFCs) across Asia and the Asian contributions to the burden of these compounds reaching the Arctic and other remote regions via long-range transport. A spatial survey of perfluorinated compounds was therefore undertaken across China, India, and Japan in 2009 using passive air samplers. Target analytes were fluorotelomer olefins (FTOs), acrylates (FTAs), alcohols (FTOHs), sulfonamides, and sulfonamidoethanols. Wide variations in concentrations and mixtures of compounds were apparent from the study. Generally the FTOHs were the most abundant, followed by 8:2 FTO in China and Japan and by the sulfonamides in India. There was a general decline in PFC concentration from urban, rural, to remote locations. Background stations reflected regional differences in air mass composition. A site in the west Pacific Ocean exhibited a Japanese profile in which 8:2 FTO and 8:2 FTOH were predominant. In contrast, a southern Indian profile with high 4:2 FTOH concentrations was observed at a background site in southern China.

Atmospheric Short-Chain Chlorinated Paraffins in China, Japan, and South Korea

This study presents the first investigation of concentrations and congener group patterns of atmospheric short-chain chlorinated paraffins (SCCPs) throughout East Asia. Based on an absorption rate calibration experiment, a spatial survey of SCCPs was performed using passive air samplers in China, Japan, and South Korea during two separate periods in 2008. The atmospheric concentrations of SCCPs in China were clearly greater than those in Japan and South Korea, both of which exceed the levels determined for other regions of the world. C(10) components were the most abundant type of SCCPs in China, whereas C(11) components were dominant in Japan and South Korea. With respect to the total chlorine content, Cl(6) and Cl(5) were the predominant compounds in China and Japan; however, Cl(6) and Cl(7) were predominant in South Korea. A similar pattern was also found for remote sites within China, Japan, and South Korea, respectively. Together with the back-trajectories calculated for the remote sites, the results indicate that the SCCPs in the air of East Asia were mainly influenced by local sources due to their relatively low long-range atmospheric transport potential compared to other POPs.

Atmospheric Polychlorinated Naphthalenes in Ghana

A nationwide monitoring of atmospheric POPs (persistent organic pollutants) was conducted in Ghana between May and July 2010, applying polyurethane foam (PUF) disk passive air samplers (PAS). Reported here are preliminary findings on PCNs, an industrial organic contaminant currently under review for possible listing under the global chemical treaty. The present results constitute the first set of nationwide data on air PCNs from a West African country. Contrary to expectation, air PCNs levels were quite high in Ghana, at an average of 49 ± 5.4 pg/m(3). The coastal (southern) zone of Ghana appeared the most impacted, with crude open burning of waste, industrial emissions, and the harbor environment identified among possible emission factors. Tri- and tetra-CNs (the lowly chlorinated homologues) predominated in the atmosphere, altogether constituting approximately 90% of total PCN homologues composition. Increased volatilization under tropical conditions was presumed a key factor that contributed to this high atmospheric input of lowly chlorinated homologues. We further observed a significant level of fractionation of PCN homologues across the breadth of the country. The percentage composition of the lowly chlorinated homologues increased northwards, probably because of their transportation in the direction of prevailing winds. From congener profile analysis, PCN-45/36 is proposed as a possible source marker for emissions preempted by uncontrolled waste burning activities. Dioxin-like toxicity of air PCNs in Ghana was estimated to range 0.49-5.6 fg TEQ/m(3). This study brought to the fore the emerging problems of nonagricultural organohalogens that covertly might be confronting the environment in African nations like Ghana.

Atmospheric burden of organochlorine pesticides in Ghana

Organochlorine pesticides (OCPs) are subject to the Stockholm Convention on POPs and have been banned or restricted globally. In Ghana, concerns of illicit applications of some OCPs have been raised in recent times. Applying polyurethane foam (PUF) disk passive air samplers (PAS), the levels of OCPs in the atmosphere and their spatial resolution were investigated. It was the first nationwide coverage of OCPs monitoring in Ghana. ∑DDTs and endusulfans constituted the highest burden of atmospheric OCPs in Ghana, at average concentrations of 156±36 and 153±28 pg m(-3), respectively. Mirex had the lowest concentration (0.2±0.01 pg m(-3)). From the chemical signatures of the various OCPs, we deduced that DDT, endosulfans and heptachlor were freshly applied at certain sites, which were all agricultural sites. The OCPs were spatially resolved as a function of the types of crops cultivated in different areas, legacy issues and recent applications.