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Sulfur mass distribution

Sulfur mass distribution - The aerosol sampled by the LPI for sulfur analysis was impacted on vaseline-coated stainless steel strips backed by 25 mm glass discs. The sulfur mass deposited on each stage was determined by the technique of flash volatilization and flame photometric detection (FVFPD)(15). [Pg.130]

On the average, the requirements for application of the statistical technique to filter data were met. Analysis of the 254 measured particle size distributions in 1979 indicates that the fine aerosol volume distribution preserved its shape. The measured sulfur mass distribution followed that of the total submicron volume. By difference, it was assumed that the organics did the same. The low relative humidity at China Lake minimized the formation of aqueous solutions due to water condensation on the particles. Therefore, it is expected that the statistical technique can be used with some success with the China Lake filter data. [Pg.144]

It was found that the requirements were satisfied for application of the linear regression technique to species mass concentrations in a multicomponent aerosol. The results of 254 particle size distributions measured at China Lake in 1979 indicate that the normalized fine aerosol volume distribution remained approximately constant. The agreement between the calculated and measrued fine particle scattering coefficients was excellent. The measured aerosol sulfur mass distribution usually followed the total distribution for particles less than 1 ym. It was assumed that organic aerosol also followed the total submicron distribution. [Pg.152]

Aerosol was occasionally sampled with low pressure impactors (LPI s) to obtain sulfur and elemental mass distributions using the techniques described by Ouimette (13). [Pg.129]

Figure 5. Sulfur size distribution in Glendora, California (east of Los Angeles), August 1986. The period of poor visibility during August 12 through 16 is best explained by the presence of sulfur mass in sizes above 0.34 xm in diameter. Surprisingly, fine mass and most of the other components changed little as the visibility improved. (Reproduced with permission from reference 24. Copyright... Figure 5. Sulfur size distribution in Glendora, California (east of Los Angeles), August 1986. The period of poor visibility during August 12 through 16 is best explained by the presence of sulfur mass in sizes above 0.34 xm in diameter. Surprisingly, fine mass and most of the other components changed little as the visibility improved. (Reproduced with permission from reference 24. Copyright...
Figure 7. Sulfur size distributions at Grand Canyon National Parky August 1984, The finest aerosols are at the top (stage 8, around 0.1 xm), and the coarsest (8.5 to about 15 xm) are at the bottom. Most sulfur mass occurs between 0.34 and 0.56 xm (stage 6). The periods of August 14 are used for Table 111. (Reproduced with permission from reference 15. Copyright 1988.)... Figure 7. Sulfur size distributions at Grand Canyon National Parky August 1984, The finest aerosols are at the top (stage 8, around 0.1 xm), and the coarsest (8.5 to about 15 xm) are at the bottom. Most sulfur mass occurs between 0.34 and 0.56 xm (stage 6). The periods of August 14 are used for Table 111. (Reproduced with permission from reference 15. Copyright 1988.)...
Modeling Dynamic Hydrothermal Processes by Coupling Sulfur Isotope Distributions with Chemical Mass Transfer Approach... [Pg.226]

Polymerization temperature principally affects three characteristics of the polymer obtained from chloroprene emulsion polymerizations gel content and molar mass distribution, stereoregularity, and the tendency of the polymer to crystallize. Reducing the polymerization temperature decreases the tendency for polymer gel to form. This is illustrated by the results reported by Mochel [22], own in Figure 15.12, for polychloroprenes produced by emulsion polymerization at 10 °C and 40 °C in the presence of 0.6 parts of sulfur per 100 parts by mass of chloroprene, and before peptization with a thiuram disulfide. The onset of the formation of polymer gel is retarded by reducing the polymerization temperature whereas a substantial proportion of the polymer is gelled at only 10% conversion when polymerization is carried out at 40 C, the polymer is essentially gel-fipee up... [Pg.289]

Table 15.5 shows the results of Mochel [22] for the effect of conversion upon the gel content of polychloroprene rubbers prepared by emulsion polymerization at 40 °C. In section (a) of this table are shown results for polymers produced in the absence of added sulfur section (b) shows results for polymers produced with the addition of 0.6 parts of sulfur per 100 parts by mass of chloroprene, before chemical peptization of the polymer. In both types of reaction system, polymer gel begins to form quite early in the reaction. However, these results indicate that sulfur has a slight tendency to act as a modifier during the polymerization, in that the onset of gel-formation is delayed when sulfur is present. Also delayed is the pdnt at which the polymer is virtually entirely gel. Mochel et al. [23] have reported results for the molar mass distribution of a thiuiam-modified polychloroprene rubber produced by emulsion polymerization at 40 °C,... [Pg.695]

Ross (R2) reported measurements of desulfurization efficiency of fixed-bed pilot and commercial units operated under trickle-flow conditions. The percentage of retained sulfur is given as a function of reciprocal space velocity, and the curve for a 2-in. diameter pilot reactor was found to lie below the curves for commercial units it is argued that this is proof of bad liquid distribution in the commercial units. The efficiency of the commercial units increased with increasing nominal liquid velocity. This may be an effect either of mass-transfer resistance or liquid distribution. [Pg.104]

Figure 7. SEM and XRMA microphotographs of palladium catalysts supported on the amphiphilic resin made by DMAA, MTEA, MBAA (cross-linker) [30]. Microphotographs (a) and (b) show an image and the radial palladium distribution after uptake of [Pd(OAc)2] from water/acetone the precursor diffuses only into the outer layer of the relatively little swollen CFP after reduction the nanoclusters remain close to the edge of the catalyst beads. Microphotographs (c) and (d) show the radial distribution of sulfur and palladium, respectively, after uptake of [PdCU] from water after reduction palladium is homogenously distributed throughout the catalyst particles. This indicates that under these conditions the CFP was swollen enough to allow the metal precursor to readily penetrate the whole of polymeric mass. (Reprinted from Ref. [30], 2005, with permission from Elsevier.)... Figure 7. SEM and XRMA microphotographs of palladium catalysts supported on the amphiphilic resin made by DMAA, MTEA, MBAA (cross-linker) [30]. Microphotographs (a) and (b) show an image and the radial palladium distribution after uptake of [Pd(OAc)2] from water/acetone the precursor diffuses only into the outer layer of the relatively little swollen CFP after reduction the nanoclusters remain close to the edge of the catalyst beads. Microphotographs (c) and (d) show the radial distribution of sulfur and palladium, respectively, after uptake of [PdCU] from water after reduction palladium is homogenously distributed throughout the catalyst particles. This indicates that under these conditions the CFP was swollen enough to allow the metal precursor to readily penetrate the whole of polymeric mass. (Reprinted from Ref. [30], 2005, with permission from Elsevier.)...
Novakov and Penner (1993) measured the mass size distributions of sulfur, organic carbon, and chlorine (characteristic of sea salt) as well as the CCN concentration (at 0.5% supersaturation), nss, and Aitken nuclei concentrations at a mountain peak in Puerto Rico. [Pg.810]

Wiener Powders (Baked Powders). Introduced in Russ in 1873, they were prepd by compression of the usual ingredients of BlkPdr, preheated to 120°. This was done in order to melt the sulfur, and thus achieve its better distribution thruout the mass... [Pg.380]

Such reactions can take place predominantly in either the continuous or disperse phase or in both phases or mainly at the interface. Mutual solubilities, distribution coefficients, and the amount of interfadal surface are factors that determine the overall rate of conversion. Stirred tanks with power inputs of 5-10 HP/1000 gal or extraction-type equipment of various kinds are used to enhance mass transfer. Horizontal TFRs usually are impractical unless sufficiently stable emulsions can be formed, but mixing baffles at intervals are helpful if there are strong reasons for using such equipment. Multistage stirred chambers in a single shell are used for example in butene-isobutane alkylation with sulfuric acid catalyst. Other liquid-liquid processes listed in Table 17.1 are numbers 8, 27, 45, 78, and 90. [Pg.595]

By this method a more homogenous and compact mass was obtained than in ordinary BkPdr because the sulfur melted and was distributed more uniformly betw the K nitrate and charcoal. As this method of manuf was dangerous it was abandoned in 1878 Re/ Daniel(l 902),808... [Pg.4]


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See also in sourсe #XX -- [ Pg.130 ]




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