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Subject barium

Thermal decompositions of barium and strontium azides, preirradiated with 1 MeV gamma rays, were conducted by Prout and Moore [78,79]. With dehydrated barium azide a total gamma dose of 20 Mrad (2.24 X 10 R) eliminated the induction period and increased the acceleration of the decomposition. A somewhat greater effect was evidenced with strontium azide. Avrami et al. [80] subjected barium azide to Co gamma radiation to exposure levels up to 1 XIO R (Table XIII). Differential thermal analyses (Figure 16) showed a steady decomposition of the sample, and after 1 X 10 R exposure (W hr at room temperature), infrared analysis indicated that the residue was in the form of barium carbonate. [Pg.224]

I have found that a mixture of citral and acetone, if it is subjected, in the presence of water, for a suffieiently long time to the action of hydrates of alkaline earths or of hydrates of alkali metals, or of other alkaline agents, is eondensed to a ketone of the formula CjjH pO. This substanee, which I term Pseudo-ionone," may be produced lor instance in shaking together for several days equal parts of citral and acetone with a solution of hydrate of barium, and in dissolving the products of this reaction in ether. [Pg.218]

Greases are also made from soaps of strontium, barium and aluminum. Of these, aluminum-based grease is the most widely used. It is insoluble in water and very adhesive to metal. Its widest application is in the lubrication of vehicle chassis. In industry, it is used for rolling-mill applications and for the lubrication of cams and other equipment subject to violent oscillation and vibration, where its adhesiveness is an asset. [Pg.879]

All commercial materials are based on calcium hydroxide and liquid alkyl salicylates (Prosser, Grolfman Wilson, 1982) and are supplied as a two-paste pack. Zinc oxide is sometimes added to the calcium hydroxide, as are neutral fillers. A paste is formed from this powder by the addition of a plasticizer examples include A-ethyl toluenesulphonamide (o- orp-) and paraffin oil, with sometimes minor additions of polypropylene glycol. The other paste is based on an alkyl salicylate as the active constituent containing an inorganic filler such as titanium dioxide, calcium sulphate, calcium tungstate or barium sulphate. Alkyl salicylates used include methyl salicylate, isobutyl salicylate, and 1-methyl trimethylene disalicylate. An example of one commercial material, Dycal, is given in Table 9.7, but its composition has been subjected to change over the years. [Pg.348]

The hematite with adsorbed Co-57 or Sb-119 along with the solution was subjected to emission Mossbauer measurement at 24 1°C with the experimental setup shown in Figure 2. The absorber, Fe-57-enriched potassium ferrocyanide (0.5 mg Fe-57/cm2) or barium stannate (0.9 mg Sn-119/cm2), was driven by a Hanger 700-series Mossbauer spectrometer connected to a Tracor-Northern TN-7200 multi-channel analyzer. The Mosssbauer gamma-rays of Co-57 and Sb-119 were detected respectively with a Kr(+3% carbon dioxide)-filled proportional counter and with a 2 mm-thick Nal(Tl) scintillation counter through 65 pm-thick Pd critical absorber for Sn K X-rays. The integral errors in the relative velocity were estimated to be of the order of 0.05 mm/s by repeated calibration measurements using standard absorbers. [Pg.406]

These products, usually calcium or barium Takes of acid azo-dyes co-precipitated with the abietates ( rosinates ), are subject to spontaneous ignition, either in the freshly ground state, or as bulk material in drying ovens while a little moisture remains. [Pg.375]

Barium azide may be prepared by reacting sodium azide with a soluble barium salt. The solution is concentrated to allow crystals grow. Crystals wdl explode if fully dried, or subject to friction. Product should be stored damp with ethanol. [Pg.80]

Barium titanate is made by sintering a finely powdered mixture of barium carbonate and titanium dioxide in a furnace at 1,350°C. The calcined mass is finely ground and mixed with a binder (plastic). The mixture is subjected to extrusion, pressing or film casting to obtain ceramic bodies of desired shapes. Plastic is burnt off by heating and the shaped body is sintered by firing and then pobshed. [Pg.95]

Acid soluble rare earth salt solution after the removal of cerium may be subjected to ion exchange, fractional crystalhzation or solvent extraction processes to separate individual rare earths. Europium is obtained commercially from rare earths mixture by the McCoy process. Solution containing Eu3+ is treated with Zn in the presence of barium and sulfate ions. The triva-lent europium is reduced to divalent state whereby it coprecipitates as europium sulfate, EuS04 with isomorphous barium sulfate, BaS04. Mixed europium(ll) barium sulfate is treated with nitric acid or hydrogen peroxide to oxidize Eu(ll) to Eu(lll) salt which is soluble. This separates Eu3+ from barium. The process is repeated several times to concentrate and upgrade europium content to about 50% of the total rare earth oxides in the mixture. Treatment with concentrated hydrochloric acid precipitates europium(ll) chloride dihydrate, EuCb 2H2O with a yield over 99%. [Pg.295]

In conclusion, the bis-barium complex of 17 catalyzes the ethanolysis of anilide and ester substrates endowed with a distal carboxylate anchoring group (Table 5.7). The catalyst shows recognition ofthe substrate, induces fairly high reaction rates with catalytic turnover, and is subjected to competitive inhibition by carboxylate anions, as... [Pg.130]

Figures 1 through 5 should, therefore, be considered as representative values which (especially at values of Cj less than 10 mg-atom/ml) might be subject to variations on the order of 0.5 log units. Furthermore, the assumption that the solid-phase concentrations of rubidium, strontium and barium given in Table I represented the concentrations of sorbed species introduces further... Figures 1 through 5 should, therefore, be considered as representative values which (especially at values of Cj less than 10 mg-atom/ml) might be subject to variations on the order of 0.5 log units. Furthermore, the assumption that the solid-phase concentrations of rubidium, strontium and barium given in Table I represented the concentrations of sorbed species introduces further...
The three samples with the optimum reagent ratios (Ratio A, B, and C) were subjected to TCLP analysis and the leachate was analyzed for arsenic, barium, cadmium, chromium, cobalt, lead, mercury, nickel, selenium and silver. [Pg.367]

Various modifications by which the reaction with barium chloride may be subjected to volumetric treatment have been suggested.4 Thus the precipitant may be added in excess and suitably back-titrated.5... [Pg.178]


See other pages where Subject barium is mentioned: [Pg.434]    [Pg.351]    [Pg.279]    [Pg.483]    [Pg.283]    [Pg.464]    [Pg.41]    [Pg.121]    [Pg.423]    [Pg.556]    [Pg.816]    [Pg.45]    [Pg.287]    [Pg.487]    [Pg.166]    [Pg.340]    [Pg.241]    [Pg.48]    [Pg.177]    [Pg.103]    [Pg.188]    [Pg.465]    [Pg.4]    [Pg.74]    [Pg.516]    [Pg.279]    [Pg.78]    [Pg.357]    [Pg.303]    [Pg.321]    [Pg.533]    [Pg.719]    [Pg.720]    [Pg.326]    [Pg.848]    [Pg.1093]    [Pg.1133]   
See also in sourсe #XX -- [ Pg.149 , Pg.153 , Pg.156 , Pg.188 ]




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