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Calcium filter

Calcium in calcium carbonate. Determine the calcium in an analysed sample of dolomite. Dissolve about 0.38 g, accurately weighed in 1 1 hydrochloric acid, warm gently, filter through a quantitative filter paper, wash, dilute the combined filtrate and washings to 1 L. Measure the calcium content of the resulting solution use a calcium filter. Compare the value for Ca thus obtained with the known Ca content. [Pg.813]

Calcium is freely filtered along with other components of the plasma through the nephrons of the kidney. Most of this calcium is reabsorbed into the blood from the proximal tubule of the nephron. However, because the kidneys produce about 1801 of filtrate per day, the amount of calcium filtered is substantial. Therefore, the physiological regulation of even a small percentage of calcium reabsorption may have a significant effect on the amount of calcium in the blood. Parathyroid hormone acts on the Loop of Henle to increase the reabsorption of calcium from this segment of the tubule and... [Pg.131]

Calcium. Excess calcium can occur in wines stored in concrete tanks or otherwise exposed to calcium (filter aids, calcium bentonite, etc.). After fortified wines are bottled, calcium tartrate may slowly precipitate. [Pg.152]

Almost aU of the 240 mmol of calcium filtered daily in the kidney is reabsorbed by three mechanisms (Friedman, 2000) ... [Pg.94]

Industrially. phosphoric(V) acid is manufactured by two processes. In one process phosphorus is burned in air and the phos-phorus(V) oxide produced is dissolved in water. It is also manufactured by the action of dilute sulphuric acid on bone-ash or phosphorite, i.e. calcium tetraoxophosphate(V). Ca3(P04)2 the insoluble calcium sulphate is filtered off and the remaining solution concentrated. In this reaction, the calcium phosphate may be treated to convert it to the more soluble dihydrogenphosphatc. CafHjPOjj. When mixed with the calcium sulphate this is used as a fertiliser under the name "superphosphate . [Pg.246]

Addition of calcium nitrate solution to a fluoride gives a white precipitate of calcium fluoride, CaFj. If the latter is precipitated slowly, it can be filtered off and weighed to estimate the fluoride. Fluoride can also be determined by the addition of sodium chloride and lead nitrate which precipitate lead chlorofluoride, PbClF. This is filtered off and weighed. [Pg.348]

Run off the lower layer of bromide, dry it with calcium chloride (as in the above preparation of ethyl bromide) and finally distil the filtered bromide from a small flask, preferably through a short column. Collect the n-butyl bromide as a colourless liquid of b.p. 99-102°. Yield, 30 g. [Pg.103]

The benzene used in this preparation should be reasonably free from toluene therefore use a sample of benzene supplied by dealers as crystalUsable benzene, i.e.y one which crystallises readily when cooled in ice-water. It should preferably be dried over calcium chloride and, immediately before use, filtered through a fluted filter-paper. The pyridine should also preferably be dried over solid potassium hydroxide and redistilled. [Pg.175]

Dissolve 13 g. of sodium in 30 ml. of absolute ethanol in a 250 ml. flask carrying a reflux condenser, then add 10 g. (9 5 ml.) of redistilled ethyl malonate, and place the flask on a boiling water-bath. Without delay, add a solution of 5 3 g. of thiourea in a minimum of boiling absolute ethanol (about 100 ml.). The sodium salt of thiobarbituric acid rapidly begins to separate. Fit the water-condenser with a calcium chloride guard-tube (Fig. 61, p. 105), and boil the mixture on the water-bath for 1 hour. Cool the mixture, filter off the sodium salt at the pump and wash it with a small quantity of cold acetone. Dissolve the salt in warm water and liberate the acid by the addition of 30 ml. of concentrated hydrochloric acid diluted with 30 ml. of water. Cool the mixture, filter off the thiobarbituric acid, and recrystallise it from hot water. Colourless crystals, m.p. 245 with decomposition (immersed at 230°). Yield, 3 5 -4 0 g. [Pg.307]

In practice, it is best to purify a quantity, say one Winchester quart bottle, of technical 0 720 ether to cover the requirements of a group of students. The Winchester quart of ether is divided into two approximately equal volumes, and each is shaken vigorously in a large separatory funnel with 10-20 ml. of the above ferrous solution diluted with 100 ml. of water. The latter is removed, the ether transferred to the Winchester bottle, and 150-200 g. of anhydrous calcium chloride is added. The mixture is allowed to stand for at least 24 hours with occasional shaking. Both the water and the alcohol present are thus largely removed. The ether is then filtered through a large fluted filter paper into another clean dry Winchester bottle (CAUTION all flames in the vicinity must be... [Pg.163]

The acetone is refluxed with successive small quantities of potassium permanganate until the violet colour persists. It is then dried with anhydrous potassium carbonate or anhydrous calcium sulphate, filtered from the desiccant, and fractionated precautions are taken to exclude moisture. [Pg.171]

Benzene. The analytical reagent grade benzene is satisfactory for most purposes if required dry, it is first treated with anhydrous calcium chloride, filtered, and then placed over sodium wire (for experimental details, see under Diethyl ether, 1). [Pg.172]


See other pages where Calcium filter is mentioned: [Pg.166]    [Pg.313]    [Pg.166]    [Pg.1930]    [Pg.53]    [Pg.166]    [Pg.417]    [Pg.166]    [Pg.313]    [Pg.166]    [Pg.1930]    [Pg.53]    [Pg.166]    [Pg.417]    [Pg.40]    [Pg.77]    [Pg.78]    [Pg.79]    [Pg.91]    [Pg.105]    [Pg.106]    [Pg.110]    [Pg.158]    [Pg.176]    [Pg.180]    [Pg.185]    [Pg.190]    [Pg.220]    [Pg.237]    [Pg.253]    [Pg.255]    [Pg.256]    [Pg.259]    [Pg.266]    [Pg.273]    [Pg.274]    [Pg.277]    [Pg.310]    [Pg.128]    [Pg.140]    [Pg.141]    [Pg.159]    [Pg.164]    [Pg.172]    [Pg.172]   
See also in sourсe #XX -- [ Pg.89 ]




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