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Bresnahan, PJ, Martz TR.  2018.  Gas diffusion cell geometry for a microfluidic dissolved inorganic carbon analyzer. Ieee Sensors Journal. 18:2211-2217.   10.1109/jsen.2018.2794882   AbstractWebsite

Variable gas diffusion cell geometries were tested for the extraction of dissolved inorganic carbon (DIC) from a microfluidic (tens to hundreds of microliters) seawater sample. With a focus on optimization of diffusion cell geometry, we compare five unique diffusion cell designs. Using 3-D printing technology to streamline the prototyping and testing process, we were able to conceive, design, fabricate, and thoroughly evaluate each design over the course of about one month. In total, 1043 DIC measurements were carried out in 109 experiments for the five working manifolds. We find that a small diameter, cylindrical diffusion cell design offers several advantages over its planar counterparts and a larger diameter cylindrical cell, most notably the ability to increase the ratio of the exchange membrane's contact surface area to solution volume (the "aspect ratio") without sacrificing channel integrity. Multiple designs approached short-term repeatability of <1%, but only the cylindrical diffusion cell design allowed for <0.2% repeatability using less than 200 mu L of sample.

Martz, TR, Jannasch HW, Johnson KS.  2009.  Determination of carbonate ion concentration and inner sphere carbonate ion pairs in seawater by ultraviolet spectrophotometric titration. Marine Chemistry. 115:145-154.   10.1016/j.marchem.2009.07.002   AbstractWebsite

We describe a novel method for determination of carbonate ion concentration in seawater by acidimetric titration with UV detection. Because CO(3)(2-) absorbs light at wavelengths of less than similar to 250 nm, it is feasible to titrate most carbonate-containing natural waters with acid and observe an increase in %Transmittance. The observed signal is proportional to the concentration of carbonate ion in the original sample. Present technology permits a theoretical precision in the determination of [CO(3)(2-)] in natural seawater background of similar to 0.5% (at 10 cm pathlength, 200 mu M CO(3)(2-), +/- 0.0001 AU). The procedure has been tested at 1 and 10 cm pathlengths using single and multipoint titration methods, respectively. Results using natural seawater test solutions indicate a resolution in [CO(3)(2-)] of 3.6% in a standard I cm cuvette using a very simple manual method, and 0.7% using a custom-built 10 cm closed titration cell. Estimates of the relative distribution of CO(3)(2-) between inner and outer sphere complexes with Mg(2+) and Na(+) were also determined and the equilibrium constants agree with published values. This method provides a new tool for studies of several fundamental aspects CO(2) chemistry, including the second dissociation constant of carbonic acid, CO(3)(2-) ion pairing, and can be used to directly measure the distribution of carbonate ion in seawater and many other types of natural waters. (C) 2009 Elsevier B.V. All rights reserved.