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Nitrogen concentrations, measurement

The variation of activity for these catalysts, all made under the same experimental conditions, except for the carbon support, was stunning and is presented as fuel cell polarization curves in Figure 3.25. On the one hand, the specific area of all these catalysts was measured and no correlation with the catalytic activity was found. On the other hand, there was a definite correlation between the catalytic activity and the surface nitrogen concentration measured by XPS. This correlation is illustrated in Figure 3.26. It is obvious that the catalytic activity for ORR increases when the surface of the catalyst is richer in nitrogen atoms. This is a logical result, since the precursor of the Fe-N2/C catalytic site (the most... [Pg.117]

In the dynamic method the powder is flushed with an inert gas during degassing, nitrogen is then adsorbed on the powder in a carrier of helium gas at known relative pressure while the powder is in a container surrounded by hquid nitrogen. The changing concentration of nitrogen is measured by a cahbrated conductivity cell so that the amount adsorbed can be determined. [Pg.1828]

It is calculated by measuring the nitrogen concentration in expired gas after a single breath of 100% oxygen. The nitrogen wash-out test is the same method used to measure anatomical dead space. Closing volume increases with age and reaches the standing FRC at 70 years and the supine FRC at 40 years. [Pg.116]

Prompt NO mechanisms In dealing with the presentation of prompt NO mechanisms, much can be learned by considering the historical development of the concept of prompt NO. With the development of the Zeldovich mechanism, many investigators followed the concept that in premixed flame systems, NO would form only in the post-flame or burned gas zone. Thus, it was thought possible to experimentally determine thermal NO formation rates and, from these rates, to find the rate constant of Eq. (8.49) by measurement of the NO concentration profiles in the post-flame zone. Such measurements can be performed readily on flat flame burners. Of course, in order to make these determinations, it is necessary to know the O atom concentrations. Since hydrocarbon-air flames were always considered, the nitrogen concentration was always in large excess. As discussed in the preceding subsection, the O atom concentration was taken as the equilibrium concentration at the flame temperature and all other reactions were assumed very fast compared to the Zeldovich mechanism. [Pg.423]

Although the process to determine KlA and K is possible with a spread sheet, it is cumbersome for commercial specifications. The guidehne for the testing of commercial aeration devices has been well developed and is generally available (American Society of Civil Engineers, 1992). There is no requirement to measure total dissolved gas pressure or estimate dissolved nitrogen concentration, and an... [Pg.261]

The surface nitrogen concentration [N(s)] was measured as a function of time for ammonia pressures of 124 and 1400 Pa. Calculate [N(s>] (atoms/cm2) as a function of time for these two pressures, and compare with experimental values from Ref. [425] (data can be found in the file SiNitridation, csv). Plot theory and experiment on the same graph. Take k2 = 1.5 x 10 4 s 1. [Pg.485]

Hydrolysis of N205 on sulfuric acid represents a very efficient channel for nitrogen deactivation. Measurements using large 100-pm droplet trains [75,96] and submicron sulfuric acid aerosols [73,77] indicate high uptake probalilities (y = 0.1), without strong dependence on f SO, concentration or temperature. The data were fitted into an uptake model [96], Uptake coefficients over on water-ice (y = 0.02), SAT ((y = 0.006) and NAT (y= 0.0003) are much suppressed [86,90]. [Pg.275]

Fig. 7.4. Differential effect of nutrient supply on biomass and cord development in Serpula lacrymans. The fungus was inoculated centrally on uniform defined agar media in a factorial experiment with 5,10, 20, 40 and 80g/l sucrose and 1.5, 3, 6 and 12.5 g/1 sodium aspartate. Biomass was measured as oven dry weight at 8 weeks, cords were counted crossing a circular transect 3 cm from the inoculum disc. Left to right C/N ratio of each of the twenty combinations of carbon and nitrogen concentration biomass cord development. (Adapted from Watkinson, 1975). Fig. 7.4. Differential effect of nutrient supply on biomass and cord development in Serpula lacrymans. The fungus was inoculated centrally on uniform defined agar media in a factorial experiment with 5,10, 20, 40 and 80g/l sucrose and 1.5, 3, 6 and 12.5 g/1 sodium aspartate. Biomass was measured as oven dry weight at 8 weeks, cords were counted crossing a circular transect 3 cm from the inoculum disc. Left to right C/N ratio of each of the twenty combinations of carbon and nitrogen concentration biomass cord development. (Adapted from Watkinson, 1975).
The styrene (Polysciences) was washed with 10 aqueous sodium hydroxide to remove the inhibitor and vacuum-distilled under dry nitrogen the 1-pentanol (Fisher Scientific) was dried over potassium carbonate and vacuum-distilled the potassium persulfate (Fisher Scientific) was recrystallized twice from water the 2,2 -azobls(2-methyl butyro-nltrlle) (E. I. du Pont de Nemours) was recrystallized twice from methanol the sodium dodecyl sulfate (Henkel) was used as received its critical micelle concentration measured by surface tension was 5.2 mM. Dlstllled-delonlzed water was used in all experiments. [Pg.87]

In order to quantify the loss of fixed nitrogen via denitrification and anammox we definitely need more N2 concentration measurements and more formation rate measurements in suboxic zones such as found in the Arabian Sea and the eastern tropical Pacific Ocean. [Pg.83]


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See also in sourсe #XX -- [ Pg.471 ]




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