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Coupling fluid methanol

Despite the fact that much effort has been made to model the DMFC system, considerable work remains, particularly in support of the emerging portable designs and systems. Few have treated the dominating effects of two-phase flow. No model to date has sufficient detail to provide a microfluidic theory for portable systems including effects of channel geometry and wettability characteristics of the GDL on fluid flow in the anode or cathode. Modeling studies are needed to fully elucidate the intricate couplings of methanol, water, and heat-transport... [Pg.518]

The method based on immunosorbents coupled on-line with liquid chromatography-atmospheric pressure chemical ionization mass spectrometry [109], discussed in section 9.4.2.1, has been applied to the determination of substituted urea type herbicides. Supercritical fluid extraction with methanol modified carbon dioxide has been applied to the determinants of sulfonyl urea herbicides in soil [261],... [Pg.250]

McNally and Wheeler [364] used supercritical fluid extraction coupled to supercritical fluid chromatography to determine sulfonylurea herbicides in soil. Klatterback et al. [365,366] used supercritical fluid extraction with methanol-modified carbon dioxide followed by high-performance liquid chromatography with UV detection to determine sulfonylurea herbicides obtained on a Cis solid-phase extraction disc. Alternatively the determination was carried out by gas chromatography of the dimethyl derivatives of the sulfonylurea herbicides, employing an electron capture or a NP detector on the gas chromatograph. [Pg.121]

Fig. 1 Chromatogram of PAHs, herbicides, and phenols obtained by supercritical carbon dioxide modified with methanol. [Reprinted from L. Toribio, M. J. del Nozal, J. L. Bernal, J. J. Jimenez, and M. L. Serna, Packed-column supercritical fluid chromatography coupled with solid-phase extraction for the determination of organic microcontaminants in water,... Fig. 1 Chromatogram of PAHs, herbicides, and phenols obtained by supercritical carbon dioxide modified with methanol. [Reprinted from L. Toribio, M. J. del Nozal, J. L. Bernal, J. J. Jimenez, and M. L. Serna, Packed-column supercritical fluid chromatography coupled with solid-phase extraction for the determination of organic microcontaminants in water,...
In industrial operation it is necessary, for economic reasons, to recover as much as possible the heat produced by exothermic reactions. One obvious way of doing this, mentioned earlier in Section 11.3, is to preheat the feed by means of the reacting fluid and/or the effluent. When the heat of reaction is sufficient to raise the temperature of the feed to such a value that the desired conversion is realized in the reactor without further addition of heat, the operation is called auto-thermic. Some of the most important industrial reactions like ammonia and methanol synthesis, SO2 oxidation, and phthalic anhydride synthesis, the water gas shift reaction can be carried out in an autothermic way. Coupling the reactor with a heat exchanger for the feed and the reacting fluid or the effluent leads to some special features that require detailed discussion. [Pg.501]

Figure 9.10 shows an example of a metabolomics sample separated by ambient pressure IMS coupled with TOF-MS. In this 2D spectrum, mass is plotted along the x-axis, and mobility data are plotted along the y-axis. A hot methanol extract of E. coli cells that had been separated from the extracellular fluid was used for this analysis. The hot methanol lysed the cells and produced an extract of the intercellular metabolome. This methanol extract was then diluted with a water solution of acetic acid to produce the final electrospray solution that was sprayed into the IMS for separation and detection of the metabolites by IMS-TOF-MS. [Pg.202]

Omran et al. have proposed a 3D, single phase steady-state model of a liquid feed DMFC [181]. Their model is implemented into the commercial computational fluid dynamics (CFD) software package FLUENT . The continuity, momentum, and species conservation equations are coupled with mathematical descriptions of the electrochemical kinetics in the anode and cathode channel and MEA. For electrochemical kinetics, the Tafel equation is used at both the anode and cathode sides. Results are validated against DMFC experimental data with reasonable agreement and used to explore the effects of cell temperature, channel depth, and channel width on polarization curve, power density and crossover rate. The results show that the power density peak and crossover increase as the operational temperature increases. It is also shown that the increasing of the channel width improves the cell performance at a methanol concentration below 1 M. [Pg.293]


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Fluid couplings

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