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Calcium saturated with

Commercial diethyl carbonate may be purified by the following process. Wash 100 ml. of diethyl carbonate successively with 20 ml. of 10 per cent, sodium carbonate solution, 20 ml. of saturated calcium chloride solution, and 25 ml. of water. Allow to stand for one hour over anhydrous calcium chloride with occasional shaking, filter into a dry fiask containing 5 g. of the same desiccant, and allow to stand for a further hour. Distil and collect the fraction boiling at 125-126°. Diethyl carbonate combines with anhydrous calcium chloride slowly and prolonged contact should therefore be avoided. Anhydrous calcium sulphate may also be used. [Pg.259]

Ethyl S-n-butyl xanthate. Use 32 g. of potassium ethyl xanthate, 37 g. (23 ml.) of n-butyl iodide (Section 111,40) and 50 ml. of absolute ethyl alcohol. Reflux on a water bath for 3 hours. Pour into 150 ml. of water, saturate with salt (in order to facilitate the separation of the upper layer), remove the upper xanthate layer, wash it once with 25 ml. of saturated salt solution, and dry with anhydrous calcium chloride or anhydrous calcium sulphate. Distil from a 50 ml. Claisen flask under reduced pressure. Collect the pale yellow ethyl S-n-butyl xanthate at 90-91°/4 mm. The yield is 34 g. [Pg.499]

One example of a liquid-based ion-selective electrode is that for Ca +, which uses a porous plastic membrane saturated with di-(n-decyl) phosphate (Figure 11.13). As shown in Figure 11.14, the membrane is placed at the end of a nonconducting cylindrical tube and is in contact with two reservoirs. The outer reservoir contains di-(n-decyl) phosphate in di- -octylphenylphosphonate, which soaks into the porous membrane. The inner reservoir contains a standard aqueous solution of Ca + and a Ag/AgCl reference electrode. Calcium ion-selective electrodes are also available in which the di-(n-decyl) phosphate is immobilized in a polyvinyl chloride... [Pg.482]

Brine Preparation. Sodium chloride solutions are occasionally available naturally but they are more often obtained by solution mining of salt deposits. Raw, near-saturated brines containing low concentrations of impurities such as magnesium and calcium salts, are purified to prevent scaling of processing equipment and contamination of the product. Some brines also contain significant amounts of sulfates (see Chemicals FROMBRINe). Brine is usually purified by a lime—soda treatment where the magnesium is precipitated with milk of lime (Ca(OH)2) and the calcium precipitated with soda ash. After separation from the precipitated impurities, the brine is sent to the ammonia absorbers. [Pg.523]

Health and Safety Factors. The low solubiUty of calcium fluoride reduces the potential problem of fluoride-related toxicity. Water saturated with calcium fluoride has a fluoride concentration of 8.1 ppm as compared to the recommended water fluoridation level of 1 ppm fluoride ion. However, because the solubiUty of calcium fluoride ia stomach acid is higher, continued oral ingestion of calcium fluoride could produce symptoms of fluorosis. The adopted TWA limit for fluorides as F is 2.5 mg/m (68,69). [Pg.175]

A big concern in swimming pools is prevention of etching and scaling (ie, precipitation of CaCO ) which can be controlled by maintenance of a proper degree of saturation with respect to calcium carbonate. The calcium carbonate dissolution-precipitation equiUbrium is represented by ... [Pg.300]

These three equations represent saturation with respect to the hexahydrate, tetrahydrate, and dihydrate in the temperature ranges indicated. The phase relationships among calcium chloride, its hydrates, and a saturated solution are illustrated in the diagram in Figure 1. [Pg.413]

A mixture of 50 g. (0.26 mole) of anhydrous stannous chloride and 225 ml. of dry ether is placed in a 1-1. three-necked round-bottomed flask fitted with a rubber-tube sealed stirrer, an inlet tube reaching nearly to the bottom of the flask, and a reflux condenser (Note 2) protected by a calcium chloride drying tube. The mixture is saturated with dry hydrogen chloride (Note 3) with continuous stirring. Within 3 hours all the stannous chloride dissolves, forming a clear viscous lower layer. The source of hydrogen chloride is then disconnected, and the freshly prepared imidyl chloride is transferred into the mixture with the aid of 25 ml. of dry ether (Note 4). Stirring is continued for 1 hour, and then the reactants are allowed to stand at room temperature for 12 hours. [Pg.98]

Since the reactions (15), (16), and (17) require successively higher temperatures, the blast furnace temperature is kept highest near the bottom of the furnace. Near the bottom, the temperature, is sufficiently high that the impure iron—saturated with carbon—collects there as a molten liquid. The slag, which is mainly calcium silicate, CaSi03, removes any sand in the ore through reaction with limestone, CaC03. [Pg.404]

Two absorbents are required, one for water vapour, the other for carbon dioxide. The absorbents for water vapour which are generally employed are (a) anhydrous calcium chloride (14-20 mesh), (b) anhydrous calcium sulphate ( Drierite or Anhydrocel ), and (c) anhydrous magnesium perchlorate ( Anhydrone ). Both (b) and (c) are preferable to (a) (c) absorbs about 50 per cent of its weight of water, but is expensive. Anhydrous calcium chloride usually contains a little free lime, which will absorb carbon dioxide also it is essential to saturate the U-tube containing calcium chloride with dry carbon dioxide for several hours and then to displace the carbon dioxide by a current of pure dry air before use. [Pg.477]

Benzonitrile, purchased from Aldrich Chemical Co., was distilled from calcium hydride and saturated with dry argon for at least 5 min prior to use. [Pg.65]

Desiccators are used to store chemicals that react slowly with water. Calcium sulfate chips in the bottom of the desiccator absorb water vapor from the atmosphere. The blue chips contain an indicator that turns pink when the calcium sulfate is saturated with water. [Pg.1013]

Inside newiy formed caverns, calcium carbonate precipitates from water dripping from the ceilings of the chambers. This happens when water that is saturated with carbon dioxide and calcium hydrogen carbonate comes into contact with air. Some of the dissolved CO2 escapes into the gas phase. This shifts the two equilibria to the left, and solid calcium carbonate precipitates ... [Pg.1192]

Gypsum is a relatively soft rock made of calcium sulfate. Rainwater percolates through g q)sum, dissolves some of the rock, and eventually becomes saturated with Ca ions and SOq ions. A geochemist takes a sample of groundwater from a cave and finds that it contains 8.4 X 10 M SO4 and 5.8 X 10 M Ca. (The ratio is not 1 1 because other sulfate rock contributes some of the SOq ions to the solution.) Use these data to determine the solubility product of calcium sulfate. [Pg.1311]

The most acid rain on record had pH — 2.00. Calculate the concentration of Ca - - cations in a solution formed when this rain becomes saturated with calcium carbonate. [Pg.1319]

Sometimes it may become necessary to shut-in a gas well when the demand for gas is low. In such instances, the well is shut-in for an indefinite period, after which it is reopened and production is resumed. It often has been found that the production rate of gas from the reopened well is substantially less than it was before the well was shut-in. During production, the inner wall of the production tubing will be coated with a film of condensed freshwater because of the geothermal gradient. This water flows down when production is interrupted and can cause formation damage. This may occur because clays are normally saturated with brine water and not with freshwater. This swelling can be prevented with the injection of some additive, for example, sodium chloride, potassium chloride, calcium chloride, or an alcohol or a similar organic material [1853]. [Pg.63]

Solutions of TKPP were mixed with aqueous fluids commonly encountered in drilling or completion of wells. Unlike saturated zinc bromide, concentrated TKPP solutions can be mixed in any proportion with fresh water with the only result being a decrease in solution density. Similar results were obtained with conventional oil field brines containing as much as 400 parts per million polyvalent cations, mostly calcium. Saturated solutions of calcium hydroxide also can be added to TKPP in any proportion without promoting precipitation as can concentrated hydrochloric acid solutions, conventionally used for well stimulation. The acid tends to generate a slight haze as the pH is reduced from 11.5 to approximately 8 however, this haze rapidly disappears as the pH is lowered by further addition of acid. [Pg.630]

Products of this type seem to protect the humus from rapid incorporation into new biological processes. Additional factors that appear to be associated with the accumulation of organic matter in Mollisols are high exchange capacities, saturation with calcium, an abundance of mineral colloids and a high content of minerals of the smectite group (Fenton, 1983). [Pg.39]

Some zeolites have the ability to exchange sodium for calcium and thereby function as water softeners by removing Ca2+. After the zeolite has become saturated with Ca2+, it can be renewed by washing it in a concentrated NaCl solution to restore the Na+ ions. Zeolites are also used to prepare ion exchange resins, as molecular sieves and as catalysts. [Pg.473]

Geochemical speciation modelling indicated saturation with respect to gypsum and several carbonates, slight under-saturation with respect to calcium arsenate (Ca3[As04]2) and ferrihydrite. [Pg.369]

Heats of precipitation have been employed to determine the enthalpies of sparingly soluble simple and complex fluorides for example, that of calcium fluoride by adding solid calcium chloride to a solution of excess sodium fluoride saturated with calcium fluoride (88), and of lead chlorofiuoride by adding sodium fluoride solution to a saturated lead chloride solution (50). [Pg.24]

A desiccator is a storage container used either to dry samples or, more commonly, to keep samples and crucibles dry and protected from the laboratory environment once they have been dried by other means. An indicating desiccant is a desiccant that changes color when saturated with adsorbed water. Drierite is an example of a desiccant. It is anhydrous calcium sulfate. [Pg.506]

Since the calcium chloride contains basic constituents the filling must be saturated with carbon dioxide before the absorption tube is used. For this purpose connect the side tube which leads to the water trap to the Kipp apparatus, interposing a drying tube, pass a strong current of carbon dioxide for 10 minutes, close the outlet, and allow to stand for half an hour, maintaining the pressure of the Kipp. After 200 c.c. of dry air have been drawn through the tube by means of the aspirator, the tube is ready for use. [Pg.61]


See other pages where Calcium saturated with is mentioned: [Pg.408]    [Pg.408]    [Pg.172]    [Pg.497]    [Pg.155]    [Pg.222]    [Pg.280]    [Pg.403]    [Pg.289]    [Pg.513]    [Pg.475]    [Pg.40]    [Pg.386]    [Pg.181]    [Pg.672]    [Pg.778]    [Pg.445]    [Pg.478]    [Pg.328]    [Pg.497]    [Pg.1361]    [Pg.38]    [Pg.351]    [Pg.60]    [Pg.187]    [Pg.33]    [Pg.282]   
See also in sourсe #XX -- [ Pg.255 , Pg.259 ]




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