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Science News - December 22, 2004
Another route to PFOA
Microbial degradation can produce small amounts of perfluorooctanoic acid (PFOA)
from fluorotelomer alcohols, according to research [for Web: recently posted to
ES&T’s Research ASAP website (es049466y).
The laboratory results are in accord with new data from sewage treatment plants
and create a fuller picture of how these substances may be moving throughout the
environment.
Fluorotelomer alcohols are volatile chemicals used to make fluorinated stain
repellents that are widely applied to fabrics, carpets, and paper. They are also
used in the manufacture of products such as paints, adhesives, waxes, polishes,
metals, electronics, and caulks. During 2000–2002, an estimated 5 million
kilograms of the telomer alcohols were produced annually worldwide, with 40% of
that production in North America.
University of Toronto chemist Scott Mabury and colleagues have theorized that
these alcohols undergo atmospheric transport and degradation to form perfluorinated
carboxylates, or perfluorocarboxylates, including PFOA, whose presence in remote
areas is of intense interest (Environ. Sci. Technol. 2004, 38,
11A–12A).
The U.S. EPA is currently completing a human health risk assessment of PFOA because
of concerns about possible developmental effects.
The new study’s lead author, Ning Wang, is a biologist at DuPont, which
uses telomer alcohols to produce stain repellent. Wang and his colleagues conducted
aerobic biodegradation studies of telomer alcohol labeled with carbon-14 in diluted
activated sludge from a wastewater treatment plan. They tracked the metabolites
using a radioisotope counting technique and then identified the degradation products
via mass spectrometry. In addition to PFOA, they identified a number of polyfluorinated
telomer acids.
Wang’s results and a paper by Mary-Joyce Dinglasan and colleagues at
the University of Toronto (Environ. Sci. Technol. 2004, 38,
2857–2864)
present a consistent picture, according to Mabury, an author of the Dinglasan
paper. “The Wang study confirms our findings and fleshes out the picture
by identifying a new degradation product,” says Mabury. In follow-up experiments,
he says, his lab has started with the dominant byproduct, the telomer acid, and
followed its eventual degradation to perfluorocarboxylates.
The degradation studies complement data from a survey of 10 U.S. urban sewage
treatment plants conducted by Oregon State University chemist Jennifer Field and
her student Melissa Schultz. The levels of carboxylates in sewage-plant effluents
were higher than influent levels in 8 out of 10 plants; this suggests that microbes
in the plant are degrading telomer alcohols, Schultz said at the Society of Environmental
Toxicology and Chemistry’s annual meeting in Portland, Ore., last month.
—REBECCA RENNER |