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Solution of Lime

The rat LD qS are 13, 3.6 (oral) and 21, 6.8 (dermal) mg/kg. Parathion is resistant to aqueous hydrolysis, but is hydroly2ed by alkah to form the noninsecticidal diethjlphosphorothioic acid and -nitrophenol. The time required for 50% hydrolysis is 120 d ia a saturated aqueous solution, or 8 h ia a solution of lime water. At temperatures above 130°C, parathion slowly isomerizes to 0,%diethyl 0-(4-nitrophenyl) phosphorothioate [597-88-6] which is much less stable and less effective as an insecticide. Parathion is readily reduced, eg, by bacillus subtilis ia polluted water and ia the mammalian mmen to nontoxic 0,0-diethyl 0-(4-aminophenyl) phosphorothioate, and is oxidized with difficulty to the highly toxic paraoxon [511-45-5] diethyl 4-nitrophenyl phosphate d 1.268, soluble ia water to 2.4 mg/L), rat oral LD q 1.2 mg/kg. [Pg.282]

Quicklime, CaO, has a density range of approximately 55 to 75 Ib/cu ft, and a molecular weight of 56.08. A slurry for feeding, called milk of lime, can be prepared with up to 45 percent solids. Lime is only slightly soluble, and both lime dust and slurries are caustic in nature. A saturated solution of lime has a pH of about 12.4. [Pg.101]

Neutral solutions also contain a dissolved salt, derived from the neutralization of the acid and the base (a salt is an ionic compound formed in a neutralization reaction and is composed of the cation of an alkali and the anion of an acid). When a solution of carbonic acid (formed when atmospheric carbon dioxide dissolves in water), for example, reacts with an alkaline solution of lime, the two solutions neutralize each other and form a salt, calcium carbonate ... [Pg.249]

Absorbent availability could have significant impact upon process costs. Most spent alkali streams could be used depending on the other impurities present. Corrosion or precipitation tests should be considered for these cases. Any other readily available alkali, like sodium carbonate or sodium hychloride, should be considered. Slurry solutions of lime or limestone should be avoided because of past operating problems. [Pg.36]

Caution. Solutions of LiMe are flammable, and SMe2 is toxic and has an unpleasant odor. [Pg.164]

Wood charcoal is preferred, and this is immersed In a saturated aqueous solution of lime, for not loss than fifteen minutes, after which it is termed by the patentee prepared charcoal The apparatus tn which this is heated, and in which the gas passes over the charcoal, is of. cost-iron, and iB represented in Figs. 128,129, and 130. It is divided into separate compnrtmonta, a a, by... [Pg.170]

In many parts of France and Belgium, they employ a weals solution of lime to assist in cleansing and freshening the hides, with the view, at the same time, of rendering the succeeding operations of depilation and tanning more easy and efficacious. [Pg.512]

I told you, when we last met, a good deal about carbonic acid. We found, by the lime-water test, that when the vapour from the top of the candle or lamp was received into bottles, and tested by this solution of lime-water (the composition of which I explained to you, and which you can make for yourselves), we had that white opacity which was in fact calcareous matter, like shells and corals, and many of the rocks and minerals in the earth. But I have not yet told you fully and clearly the chemical history of this substance—carbonic acid—as we... [Pg.160]

Monobasic calcium phosphate [Ca(H2P04)2] is manufactured by crystallization after evaporation and cooling of a hot solution of lime [CaO or Ca(OH)2] and strong phosphoric acid (H3P04). The crystals are centrifuged, and the highly acidic mother liquor returned for reuse. This acid salt is also made by spray drying a slurry of the reaction product of lime and phosphoric acid. [Pg.134]

They are not precipitated from an acid solution by water, and thus differ from the disulphonic acid. In order to isolate them, the sulphuric-acid solution is neutralised with chalk, and the precipitated calcium sulphate filtered off. The solution of lime-salt is then converted into sodium-salt. [Pg.127]

The presence of carbon dioxide can easily be determined by allowing the gas to pass through a solution of lime water. When carbon dioxide passes through such a solution a white, curdy precipitate is produced which forms in clouds. This precipitate is calcium carbonate. A very simple experiment which will illustrate... [Pg.25]

Hair removal using a solution of lime and sodium sulfide. [Pg.244]

Tests for Lime. The alkaline carbonates, phosphates, oxalates, and sulphates, occasion white precipitates in solutions of lime. The precipitates occasioned by the first three tests are soluble in dilute nitric or mnriatio acid that by the last is insoluble in those menstrua, bat soluble in solution of Bait, and not reprecipitated by dilate sulphuric acid. [Pg.256]

Temperature exerts a considerable influence in the solution of bodies, and though in a few instances, as in the solution of lime, magnesia and anhydrous sulphate of soda in water, its elevation impairs the power of the solvent, yet, as an almost universal rule, it facilitates its action. The temperature must be adapted to the nature of the solvent and the substance to be dissolved, and of the solution formed. [Pg.378]

Anderson and Vernon [27.1] reported that the rate of solution of lime increased as the mean apparent density decreased and as the particle size was reduced. For a given quicklime, reactivity correlated with mean apparent density (see Fig. 13.2), but reactivity was not the fundamental parameter. Moreover, reactivity could be affected by absorption of atmospheric water and carbon dioxide (see section 13.2). [Pg.307]

Perchloride of Mercury. 18 grains. Solution of Lime.10 fluid ounces. [Pg.156]

In the presence of lime water, carbon dioxide forms calcium carbonate. This is insoluble in water, so it precipitates out of solution. To test this, breathe through a straw into a solution of lime water, like blowing bubbles. This works according to the following formula ... [Pg.324]

Gloss oil n. Solution of limed rosin or lined rosin acids in a volatile solvent, used chiefly in surface coatings (when made from tall oil, the source is usually indicated). [Pg.461]

EUSOL (Edinburgh Solution of Lime). This contains chlorinated lime at 1.25% concentration (30% of available chlorine) and boric acid at 1.25% in aqueous solution. Whether in a pure state or in combination with liquid paraffin, EUSOL is employed in ulcer treatment however, because of its cytotoxicity, it is used only in the black and yellow phases of wound healing. Both forms are often used in chronic ulcer treatment. [Pg.468]

A few coordination compounds had been known for many years as a result of accidental discoveries. The first recorded observation of the deep blue colour of the tetraamminecopper(ll) ion was made in the sixteenth century by Andreas Libavius when he left some brass standing in a solution of lime water saturated with sal ammoniac (ammonium chloride). Prussian blue was obtained accidentally in 1704 by Diesbach, a manufacturer of artists pigments. It was the cobalt-ammine complexes which were to play such an important role in chemical theory, and the first of these to be isolated in the solid state was the compound now known as hexaamminecobalt(lll) oxalate, [Co(NH3)5]2(C204)3. This was described in 1822 by Leopold Gmelin (1788-1853). [Pg.190]

Inspection of reactions 1-4 and 6 illustrates that calcium carbonate crystals precipitated from a saturated solution of lime in water (6) contain carbon atoms present in the air at the time of the reactions (1). Thus the radiocarbon analysis records the carbon contained in the air at the time of the crystal precipitation. [Pg.23]


See other pages where Solution of Lime is mentioned: [Pg.234]    [Pg.72]    [Pg.27]    [Pg.127]    [Pg.529]    [Pg.537]    [Pg.198]    [Pg.47]    [Pg.92]    [Pg.25]    [Pg.56]    [Pg.44]    [Pg.83]    [Pg.251]    [Pg.81]    [Pg.126]    [Pg.156]    [Pg.276]    [Pg.66]   
See also in sourсe #XX -- [ Pg.142 ]




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