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Coarse sulfur

As an indication of the effect of dust storm episodes on the aerosol concentration in the valley, the per cent Increase in the weekly total mass, coarse sulfur, chlorine, silicon, and iron concentration during a dust storm was computed. In addition, the absolute Increase in these quantities was also computed. The results of this analysis are shown in Table II. These data also indicate that a significant increase in aerosol concentration due to suspended lake bed materials occurs as far downwind as Independence. In order to quantify this effect, the sulfur to iron (S/Fe) and chlorine to iron (Cl/Fe) ratio at each site was examined. At Keeler, all the coarse sulfur and iron measured at the sampling site are suspended from the lake bed. At any site... [Pg.336]

After cleaning to remove coarse material, ie, cobs, and fines (broken com, dust, etc), the com is steeped in a sulfurous acid solution to soften the com and render the starch granules separable from the protein matrix that envelopes them. About 7% of the kernel s dry substance is leached out during this step, forming protein-rich steep-water, a valuable feed ingredient and fermentation adjunct. [Pg.359]

The coarse calciae cooler operates at 300°C, while the waste-heat boiler cools the gas to 350°C. The tubes ia the boilers have a chain-shaking arrangement operated by paeumatic hammers. Steam productioa is 0.78 kg/kg of dry coaceatrate. The only trouble with dust reported is ia the connection betweea the reactor and waste-heat boiler. It is necessary to cool the gas stream quickly to avoid sulfation, but even so the carry-over calciae coataias oa the order of four times more sulfate than the coarse overflow. In this plant, the composite calciae is 0.1% sulfide and 2.2% sulfate sulfur. [Pg.400]

In the United States boric acid is produced by United States Borax Chemical Corp. in a 103,000 2 3 ric ton per year plant by reacting cmshed kernite ore with sulfuric acid. Coarse gangue is removed in rake classifiers and fine gangue is removed in thickeners. Boric acid is crystallised from strong hquor, nearly saturated in sodium sulfate, in continuous evaporative crystallizers, and the crystals are washed in a multistage countercurrent wash circuit. [Pg.194]

Parts of diallyl-barbituric acid are added to a precooled mixture of 1 5.5 parts of concentrated sulfuric acid and 0.5 part of water while stirring intensively, the mixture being cooled so that its temperature does not exceed 25°C. The honey-colored viscous solution Is stirred vigorously and all at once into 45 parts of water, whereupon the mixture warms up to 35°C to 40°C and, after several seconds, solidifies into a thick pulp, which Is then heated as quickly as possible to 95°C, at which temperature a clear solution Is formed. This is cooled slowly until the 5-allyl-5-((3-hydroxypropyl)-barbituric acid begins to form coarse-grained crystals, after which the mass is cooled rapidly to 20°C. [Pg.1327]

The large amount of S in the particles suggested that S02 gas molecules or small sulfur-containing particles condense on to the surface of soil dusts during their transportation from China. Figure 4.22 illustrates an elemental map for Si distribution in coarse particles within a total scanning area of 25 pm x 25 pm. The scale bar shows the peak count of characteristic X-rays by pixel of the scan area. [Pg.103]

Fine particulates Coarse particulates Sulfur oxides Reduced sulfur gases Volatile organic compounds Nitrogen oxides... [Pg.875]

Fiber-bed scrubbers are used to collect fine or soluble particulate matter or as mist eliminators to collect liquid aerosols, including inorganic (e.g., sulfuric acid mist) and volatile organic compounds. Insoluble or coarse PM will clog the fiber bed with time, and VOCs that are difficult to condense will not be collected efficiently. [Pg.236]

A mixture of 5 g. of anhydrous zinc chloride (Note 1) and 280 g. (2.00 moles) of 3-hydroxy-2,2,4-trimethyl-3-pentenoic acid /9-lac-tone 2 is placed in a 500-ml. three-necked flask equipped with a sealed stirrer (Note 2), a coarse fritted-glass gas-dispersion thimble, a thermometer immersed in the liquid, and an air-cooled reflux condenser (Note 3). The outlet of the condenser is connected to a bubble counter filled with concentrated sulfuric acid this in turn is vented to the atmosphere through a water scrubber. The flask is immersed in an ice bath, and stirring is started. When the temperature of the mixture is about 10°, anhydrous hydrogen chloride is introduced through the gas-dispersion tube... [Pg.64]

The lower explosive limit and minimum explosive concentrations of flax, wool, cotton, jute, hemp and sisal fibres are of the same order of magnitude as those of highly explosive dusts [15], The explosibility of pyrites dusts with sulfur contents above 20% was evaluated experimentally. Dusts of 30% sulfur content gave explosion pressures of 3 bar at pressure rise rates of 16 bar/sec. Mixtures of 60% pyrites and 40% powdered limestone still showed significant pressure effects, and the proportion of limestone actually needed to suppress explosions was considerably above the values currently accepted by mining industries [16], Effects of mixtures of particle sizes in combustible dusts upon minimum ignition temperature (T ") and upon presence or absence of explosion were studied. Presence of 30% of fines in a coarse dust lowers Tf significantly [17], Experimental explosions of polyethylene,... [Pg.133]

In a 3-1., three-necked, round-bottomed flask fitted with a powerful slow-speed stirrer having a Teflon blade, a 500-ml. dropping funnel, and a thermometer arranged to dip into the liquid is placed 588 g. (366 ml., 6 moles) of concentrated sulfuric acid. The flask is surrounded by an ice-salt mixture, the stirrer started, and 1216 g. (1170 ml., 12 moles) of acetic anhydride (Note 1) is added at such a rate that the temperature does not rise above 20° (Note 2). The separatory funnel is removed and 912 g. (6 moles) of coarsely powdered D,L-camphor is added (Note 3). The flask is then closed with a stopper and stirring is continued until the camphor is dissolved. The stirrer is replaced by a stopper, the ice bath allowed to melt, and the mixture left to stand for 36 hours (Note 4). The camphorsulfonic acid is collected on a suction filter and washed with ether (Note 5). After being dried in a vacuum desiccator at room temperature, the nearly white crystalline product weighs 530-580 g. (38-42%). It melts at 202-203° with rapid decomposition and is relatively pure (Note 6). [Pg.7]

Two bituminous coals of moderate ash content were chosen for this paper to illustrate this method of determining coal-mineral association. The first sample was an Upper Freeport coal with 1.3% moisture, 9.88% ash, and 1.56% total sulfur. The second sample was an Indiana No. 3 coal having 10.5% moisture, 7.35% ash, and 4.26% total sulfur. Both coals had been precleaned at a coarse particle size, ground to minus 325 mesh (44 ym), and then separate samples were cleaned by float-sink and by froth flotation techniques, as described elsewhere [5]. Analyses of the feed coals are included in Table I. [Pg.33]

The refined source profiles that best reproduced the coarse fraction are listed in table 7. The calculated profiles of the two crustal components follow those of Mason ( ), though the calcium concentration of 20 in the limestone factor is less than the reported value. The paint pigment profile strongly resembles that calculated for the fine-fraction data. The only major difference is that unlike the fine fraction, the coarse-fraction profile does not associate barium with the paint-pigment factor. The calculated sulfur concentration in the coarse-fraction sulfate factor is much less than that in the fine-fraction and there are sizable concentrations of elements such as aluminum, iron, and lead not found in the fine-fraction profile. The origin of this factor is not clear although as described earlier a possible explanation is that a small part of the sulfate particles in the fine fraction ended up in the coarse samples. [Pg.40]

Steeping and wet-milling processes are also utilized to separate soluble compounds from com. One process involves removal of soluble starch and protein from com by steeping com in a warm sulfurous acid solution for about one to two days. The undissolved com solids are then coarsely wet-milled and processed to collect the oil-containing germ for com oil production. Also, for more enzyme-resistant cellulose biomass, sulfuric acid or hydrochloric acid can be used to digest the cellulose polysaccharide into fermentable molecules. [Pg.280]

Sulfate shows two peaks, one in the coarse particle mode associated with sea salt, and one in the fine particle mode. The smaller peak is expected since the nss-S04 is formed from the oxidation of S02 and other sulfur-containing compounds such as dimethyl sulfide. The small size of particles containing ammonium reflects the uptake of the gaseous base NH3 into the smaller acidic particles. [Pg.384]

Similar data for sulfate have been reported in many studies. Figure 9.36, for example, shows overall average sulfate distributions measured in marine areas as well as at continental sites (Milford and Davidson, 1987). The marine data show two modes, a coarse mode associated with sea salt and a fine mode associated with gas-to-particle conversion. Sulfate in seawater, formed, for example, by the oxidation of sulfur-containing organics such as dimethyl sulfide, can be carried into the atmosphere during the formation of sea salt particles by processes described earlier and hence are found in larger particles. The continental data show only the fine particle mode, as expected for formation from the atmospheric oxidation of the S02 precursors. [Pg.384]

HC1 and heat to boiling. If the soln is not clear, filter a portion thru a coarse filter paper, heat ca 100 ml of the clear soln to boiling, and add slowly 10 ml of 50% sulfuric acid. A white ppt indicates barium, which can be confirmed by the grn color obtd in a flame test. Filter and add to the cool filtrate 1 ml of coned HC1. A white ppt indicates the presence of lead... [Pg.1069]

Figure 3. Marshall stability as a function of sulfur and asphalt contents in sand-asphalt-sulfur mixes (15,). Materials used were medium-coarse sand and 150/180 pen. asphalt. All specimens were prepared with 2 hammer blows on one face only. Figure 3. Marshall stability as a function of sulfur and asphalt contents in sand-asphalt-sulfur mixes (15,). Materials used were medium-coarse sand and 150/180 pen. asphalt. All specimens were prepared with 2 hammer blows on one face only.
Figure 5. Fatigue life as a function of sulfur content for a sand-asphalt-sulfur mix. Test temperature 50°F (10°C). Test frequency 60 Hz. Materials medium-coarse sandt and 150/180 pen. asphalt. Asphalt content 6% wt (15),... Figure 5. Fatigue life as a function of sulfur content for a sand-asphalt-sulfur mix. Test temperature 50°F (10°C). Test frequency 60 Hz. Materials medium-coarse sandt and 150/180 pen. asphalt. Asphalt content 6% wt (15),...
A turbine with a preferred gas setting in the range 0.5-1.15 mm is used to produce the emulsions. The mixture may be recycled a number of times through the turbine or a series of turbines. Alternatively, a coarse dispersion may be produced and subsequently homogenized in the turbine. Although the patents cover emulsion compositions of 13-50% sulfur, 16.5-39% is the preferred range. [Pg.239]

Domergue Explosive (1889) (Fr). A mixture of coarsely ground K chlorate and sulfur Refs 1) Daniel (1902), 207 2) Giua, Trat-... [Pg.424]


See other pages where Coarse sulfur is mentioned: [Pg.331]    [Pg.336]    [Pg.339]    [Pg.331]    [Pg.336]    [Pg.339]    [Pg.52]    [Pg.323]    [Pg.126]    [Pg.400]    [Pg.423]    [Pg.254]    [Pg.478]    [Pg.48]    [Pg.273]    [Pg.369]    [Pg.68]    [Pg.97]    [Pg.172]    [Pg.88]    [Pg.454]    [Pg.30]    [Pg.333]    [Pg.336]    [Pg.341]    [Pg.383]    [Pg.385]    [Pg.126]    [Pg.200]    [Pg.200]   
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