Determination of gas bubble fractionation rates in the deep ocean by laser Raman spectroscopy
Determination of gas bubble fractionation rates in the deep ocean by laser Raman spectroscopy
Date
2004-10-29
Authors
White, Sheri N.
Brewer, Peter G.
Peltzer, Edward T.
Brewer, Peter G.
Peltzer, Edward T.
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Keywords
Instruments
Carbon dioxide
Gas flux
Chemical sensor
Carbon dioxide
Gas flux
Chemical sensor
Abstract
A new deep-sea laser Raman spectrometer (DORISS – Deep Ocean Raman In
Situ Spectrometer) is used to observe the preferential dissolution of CO2 into
seawater from a 50%-50% CO2-N2 gas mixture in a set of experiments that test a
proposed method of CO2 sequestration in the deep ocean. In a first set of
experiments performed at 300 m depth, an open-bottomed 1000 cm3 cube was
used to contain the gas mixture; and in a second set of experiments a 2.5 cm3
funnel was used to hold a bubble of the gas mixture in front of the sampling
optic. By observing the changing ratios of the CO2 and N2 Raman bands we
were able to determine the gas flux and the mass transfer coefficient at 300 m
depth and compare them to theoretical calculations for air-sea gas exchange.
Although each experiment had a different configuration, comparable results
were obtained. As expected, the ratio of CO2 to N2 drops off at an exponential
rate as CO2 is preferentially dissolved in seawater. In fitting the data with
theoretical gas flux calculations, the boundary layer thickness was determined to
be ~42 μm for the gas cube, and ~165 μm for the gas funnel reflecting different
boundary layer turbulence. The mass transfer coefficients for CO2 are kL = 2.82
x 10- 5 m/s for the gas cube experiment, and kL = 7.98 x 10- 6 m/s for the gas
funnel experiment.
Description
Author Posting. © The Authors, 2004. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Marine Chemistry 99 (2006): 12-23, doi:10.1016/j.marchem.2004.10.006.