Jiping Zhu

Sorbent-impregnated polyurethane foam disk for passive air sampling of volatile fluorinated chemicals.

A passive air sampler comprising a polyurethane foam (PUF) disk impregnated with XAD-4 powder has been developed. This sorbent-impregnated PUF (SIP) disk builds on previous work using PUF disk passive air samplers that have been effective in spatial air mapping studies of nonpolar hydrophobic chemicals, without the need of electricity or expensive air sampling equipment. In this study, PUF disks and SIP disks are calibrated for sampling volatile polyfluorinated chemicals--specifically, the fluorotelomer alcohols (FTOHs) and perfluoroalkyl sulfonamides (PFASs). Results demonstrate the low sorptive capacity of the PUF disk samplers, particularly for the FTOHs, with PUF disks reaching equilibrium within 1 day, after collecting approximately 0.4 and 1.2 m3 of air for 8:2 FTOH and 10:2 FTOH, respectively. This limits their use for these target compounds when time-weighted, linear-phase sampling is desired. The presence of just 0.4 g of XAD powder in the SIP disks greatly increases the sorptive capacity (by approximately 2 orders of magnitude for the FTOHs) and provides linear-phase sampling for a period of several weeks. PUF-air partition coefficients, KPUF-A, calculated for the FTOHs and PFASs are considerably lower than values predicted using previously established correlations against the octanol-air partition coefficient, KOA, demonstrating the unique partitioning behavior of the polyfluorinated chemicals. Using results from these calibration tests, air concentrations of FTOHs were derived from PUF disk samples that were deployed in 52 homes in Ottawa, Canada, during 2002/2003. These represent the first comprehensive measurements of FTOHs in indoor air in North America. Range and (geometric mean) air concentrations (pg m-3) were 261-28 900 (2070) for 8:2 FTOH and 104-9210 (890) for 10:2 FTOH. These air concentrations are orders of magnitude higher than observed for outdoor air, establishing indoor environments as important for human exposure and also as potential sources to the larger environment.

Measuring chemical emissions from wet products—Development of a new measurement technique

A new approach for estimating chemical emissions from wet products has been developed. The concept of such approach is that emission rates can be estimated from the amount of target chemicals in the product as a function of evaporation time. Samples were placed under a laboratory fume hood under controlled conditions (surface air velocity and temperature). Weight losses of the product were monitored and residuals at different time intervals were chemically analyzed. Emission factors of the target chemicals were then calculated based on the weight losses and residual levels of the chemicals. To demonstrate the applicability of this approach, two wet products with very different physical characteristics, one liquid and one paste-like viscous fluid, were chosen. Emissions of two principle chemicals in the products, decamethylcyclopentasiloxane (D5), and dodecamethylcyclohexasiloxane (D6) were measured. The influences of initial sample weight, surface air velocity, and temperature were investigated. The calculated emission profiles were compared with those obtained from the chamber method. The described approach could be used as an alternative screening method for emission tests of wet products, especially for compounds with low vapour pressure when sink effect poses serious challenge in traditional chamber-based emission tests.