TY - JOUR
T1 - Long-term tropospheric trend of octafluorocyclobutane (c-C4F8 or PFC-318)
AU - Oram, D.E.
AU - Mani, F.S.
AU - Laube, J.C.
AU - Newland, M.J.
AU - Reeves, C.E.
AU - Sturges, W.T.
AU - Penkett, S.A.
AU - Brenninkmeijer, C.A.M.
AU - Röckmann, T.
AU - Fraser, P.J.
PY - 2012
Y1 - 2012
N2 - Air samples collected at Cape Grim, Tasmania
between 1978 and 2008 and during a series of more recent
aircraft sampling programmes have been analysed to determine
the atmospheric abundance and trend of octafluorocyclobutane
(c-C4F8 or PFC-318). c-C4F8 has an atmospheric
lifetime in excess of 3000 yr and a global warming potential
(GWP) of 10 300 (100 yr time horizon), making it one of the
most potent greenhouse gases detected in the atmosphere to
date. The abundance of c-C4F8 in the Southern Hemisphere
has risen from 0.35 ppt in 1978 to 1.2 ppt in 2010, and is
currently increasing at a rate of around 0.03 ppt yr−1. It is
the third most abundant perfluorocarbon (PFC) in the present
day atmosphere, behind CF4 ( 75 ppt) and C2F6 ( 4 ppt).
Although a number of potential sources of c-C4F8 have been
reported, including the electronics and semi-conductor industries,
there remains a large discrepancy in the atmospheric
budget. Using a 2-D global model to derive top-down global
emissions based on the Cape Grim measurements yields a recent
(2007) emission rate of around 1.1 Gg yr−1 and a cumulative
emission up to and including 2007 of 38.1 Gg. Emissions
reported on the EDGAR emissions database for the
period 1986–2005 represent less than 1% of the top-down
emissions for the same period, which suggests there is a large
unaccounted for source of this compound. It is also apparent
that the magnitude of this source has varied considerably
over the past 30 yr, declining sharply in the late 1980s before
increasing again in the mid-1990s.
AB - Air samples collected at Cape Grim, Tasmania
between 1978 and 2008 and during a series of more recent
aircraft sampling programmes have been analysed to determine
the atmospheric abundance and trend of octafluorocyclobutane
(c-C4F8 or PFC-318). c-C4F8 has an atmospheric
lifetime in excess of 3000 yr and a global warming potential
(GWP) of 10 300 (100 yr time horizon), making it one of the
most potent greenhouse gases detected in the atmosphere to
date. The abundance of c-C4F8 in the Southern Hemisphere
has risen from 0.35 ppt in 1978 to 1.2 ppt in 2010, and is
currently increasing at a rate of around 0.03 ppt yr−1. It is
the third most abundant perfluorocarbon (PFC) in the present
day atmosphere, behind CF4 ( 75 ppt) and C2F6 ( 4 ppt).
Although a number of potential sources of c-C4F8 have been
reported, including the electronics and semi-conductor industries,
there remains a large discrepancy in the atmospheric
budget. Using a 2-D global model to derive top-down global
emissions based on the Cape Grim measurements yields a recent
(2007) emission rate of around 1.1 Gg yr−1 and a cumulative
emission up to and including 2007 of 38.1 Gg. Emissions
reported on the EDGAR emissions database for the
period 1986–2005 represent less than 1% of the top-down
emissions for the same period, which suggests there is a large
unaccounted for source of this compound. It is also apparent
that the magnitude of this source has varied considerably
over the past 30 yr, declining sharply in the late 1980s before
increasing again in the mid-1990s.
U2 - 10.5194/acp-12-261-269-2012
DO - 10.5194/acp-12-261-269-2012
M3 - Article
SN - 1680-7316
VL - 12
SP - 261
EP - 269
JO - Atmospheric chemistry and physics
JF - Atmospheric chemistry and physics
ER -