Water containers

Cyclohexane containing Water containing the DMSO the polynuclear aromatics... 

The treated water containing sodium chloride, cyanides, phenols and traces of H2S and NH3 is recycled to the crude desalting unit and used as wash water for the hydrotreaters and FCC units. 

Some clay minerals may absorb some of the water contained in the drilling mud. This will cause the clays to swe//and eventually reduce the borehole size to the point where the drill pipe becomes stuck. Prevention mud additives which prevent clay swelling e.g. potassium salt. 

Fig. XVIII-20. Spectra of pyridine adsorbed on a water-containing molybdenum oxide (IV)-Al203 catalyst L and B indicate features attributed to pyridine adsorbed on Lewis and Brpnsted acid sites, respectively. (Reprinted with permission from Ref. 191. Copyright 1976 American Chemical Society.)...

Motion, and in particular diffiision, causes a further limit to resolution [14,15]. First, there is a physical limitation caused by spins diflfiising into adjacent voxels durmg the acquisition of a transient. For water containing samples at room temperature the optimal resolution on these grounds is about 5 pm. However, as will be seen in subsequent sections, difhision of nuclei in a magnetic field gradient causes an additional... 

However, in dilute solution [H O] is virtually conslant ([H,0] = 55.5 since 1 litre of water contains 1000/18 mol of H O) and taking this into the above expression for the equilibrium constant we obtain a second constant... 

Water contains 89 % by weight of oxygen, and the outer crust of the earth contains about 47% hence air, earth and sea together contain about 50% by weight of oxygen. 

Fluorine occurs widely in nature as insoluble fluorides. Calcium fluoride occurs as jluospar or fluorite, for example in Derbyshire where it is coloured blue and called bluejohn . Other important minerals are cryolite NajAlFg (p. 141) and Jluorapatite CaFjSCaj (P04)2. Bones and teeth contain fluorides and some natural water contains traces. 

Prepare a solution of 12 5 g. of hydroxylamine hydrochloride in 20 ml. of water contained in a too ml. conical flask. Dissolve 7 g. of powdered sodium hydroxide in 20 ml. of water, cool the solution in ice-water, and then add it to that of the hydroxylamine hydrochloride. Place a thermometer in the mixed solution, and chill the flask in ice-water until the temperature of the solution is between 5 and 10 . Now add 12 ml. (9 5 gO of dry acetone (preferably from a burette to ensure... 

Arrange the adaptor D so that the end dips below the surface of about 50 ml. of water contained in a small conical flask, or beaker, which is in turn surrounded by a mixture of ice and water. Place 37 (30 g-) of ethanol and 25 ml. of water in the flask A, and... 

Add 5 g. of potassium hydrogen tartrate and 5 g. of antimony trioxide (each being finely powdered) to 30 ml. of water contained in a small flask, and boil the mixture under a reflux water-condenser for 15 minutes. Then filter hot, using a Buchner funnel and flask which have been preheated by the filtration of some boiling distilled water. Pour the clear filtrate into a beaker and allow to cool. Potassium antimonyl tartrate separates as colourless crystals. Filter, drain and dry. Yield, 5 g. The product can be recrystallised from hot water, but this is usually not necessary. 

Dissolve 5 g. of aniline hydrochloride in 120 ml. of hot water contained in a 200 ml. conical flask and then add 4 g. of potassium cyanate. Heat the solution on a water-bath for 30 minutes, adding about 1-2 g. of animal charcoal towards the end of the heating if a slight turbidity has developed. Now bring the solution quickly to the boil over a gauze, and filter it at the pump, using a Buchner funnel and flask which have been preheated by the filtration of some boiling distilled water. The clear... 

Dissolve 36 g. of sodium hydroxide in 160 ml. of water contained in a 500 ml. conical flask, and chill the stirred solution to 0-5° in ice-water. Now add io-8 ml. (32-4 g.) of bromine slowly to the stirred solution exercise care in manipulating liquid bromine ) during this addition the temperature rises slightly, and it should again be reduced to 0-5°. Add a solution of 12 g. of acetamide in 20 ml. of water, in small portions, to the stirred hypobromite solution so that the temperature of the mixture does not exceed 20° the sodium acet-bromoamide is thus obtained in the alkaline solution. Now remove the flask from the ice-water, and set it aside at room temperature for 30 minutes. 

Meanwhile assemble the apparatus shown in Fig. 62, or that in Fig. 23(D), p. 45, having a distilling-flask of at least 500 ml. capacity in either case. If an ordinary condenser C (Fig. 62) is employed, fit the lower end of the condenser by means of a short piece of rubber tubing to a small inverted funnel. Arrange the latter so that its lip is just below the surface of 25 ml. of concentrated hydrochloric acid diluted with 75 ml. of water contained in a 250 ml. beaker B the hydro-. chloric acid is thereby prevented from being sucked back into the... 

The camphorquinone can be purified in either of two ways, (i) To save time, the drained but still damp material can be recrystallised from water containing 10% of acetic acid, the hot filtered solution being cooled and vigorously stirred. The quinone separates as brilliant yellow crystals (yield, 2 5 g.), m.p. 192-194 , increased to 196-197 by a second reciystal-lisation. (ii) The crude camphorquinone can be dried in a vacuum desiccator (weight of dry quinone, 5 g.), and then recrystallised from petroleum (b.p. 100-120 ), the hot solution being filtered through a fluted paper in a pre-heated funnel. The quinone separates in beautiful crystals, m.p. 196-197 , 2 8 g. 

Dissolve 15 ml. (15-4 g.) of aniline in a mixture of 40 ml. of concentrated hydrochloric acid and 40 ml. of water contained in a 250 ml. conical flask. Place a thermometer in the solution, immerse the flask in a mixture of ice and water, and cool until the temperature of the stirred solution reaches 5°. Dissolve I2 5 g. of powdered sodium nitrite in 30 ml. of water, and add this solution in small quantities (about 2-3 ml. at a time) to the cold aniline hydrochloride solution, meanwhile keeping the latter well stirred by means of a thermometer. Heat is evolved by the reaction, and therefore a short interval should be allowed between consecutive additions of the sodium nitrite, partly to allow the temperature to fall again to 5°, and partly to ensure that the nitrous acid formed reacts as completely as possible with the aniline. The temperature must not be allowed to rise above 10°, otherwise appreciable decomposition of the diazonium compound to phenol will occur on the other hand, the temperature... 

Alternatively, if it is not desired to collect the iodobenzene, the iodosobenzene can be added to about 150 ml. of water contained in an open beaker or conical flask, and the mixture gently boiled until a clear solution is obtained and the pale yellow colour has disappeared. On cooling the iodoxybenzene rapidly separates. 

Then, while the diazonium solution is standing in ice-water, dissolve 55 g. of powdered copper sulphate (CuS04,5Ha0) in 200 ml. of water contained in a 1500 ml. flat-bottomed flask, for which a steam-distillation fitting is available for subsequent use. Place a thermometer in the copper sulphate solution and warm the latter to 60-65 . Now cautiously add a solution of 60 g. of powdered potassium cyanide in too ml. of water to the copper... 

A) Diazotisation of Anthranilic Acid, Dissolve 20 g. of anthranilic acid in a solution of 7 5 g. of anhydrous sodium carbonate in 200 ml. of water contained in a 400 ml. beaker, (The mixture may be warmed very gently with stirring to obtain a solution more rapidly, and then cooled.) Add slowly 12 g. of sodium nitrite and cool the stirred solution below 10 , Pour this cold solution slowly on to a vigorously stirred mixture of 40 ml, of concentrated hydrochloric acid and 120 g. of crushed ice in a 600 ml. beaker. 

Dissolve 2 g. of anhydrous sodium carbonate in 50 ml. of water contained in a 400 ml. beaker and add 7 g. of finely powdered crystalline sulphanilic acid (2H2O), warming the mixture gently in order to obtain a clear solution. Add a solution of 2 2 g. of sodium nitrite in 10 ml. of water and then cool the mixture in ice-water until the temperature has fallen to 5°. Now add very slowly (drop by drop) with continual stirring a solution of 8 ml. of concentrated hydrochloric acid in 15 ml. of water do not allow the temperature to rise above 10°. When all the acid has been added, allow the solution to stand in ice-water for 15 minutes to ensure complete diazotisation during this period fine crystals of the internal salt separate from the pink solution. Dissolve 4 ml. of dimethylaniline in a mixture of 4 ml. of concentrated hydrochloric acid and 10 ml. of water, cool the solution in ice-water, and add it slowly to the cold well-stirred diazo solution a pale red coloration is developed. Allow the mixture to stand for 5 minutes and then add slowly with stirring aqueous... 

The first part of this preparation (as far as the solidification of the sodium cyanoacetate) must be carried out in the fume-cupboard. Add 30 g. of monochloroacetic acid to 60 ml. of water contained in a wide evaporating-basin (about 12-15 diameter)... 

A 40% solution of formaldehyde in water containing about 15% of methanol is known as formalin". 

To I ml. of paraldehyde in a test-tube add 5 ml. of dil. HjSO and distil gently into cold water contained in another test-tube (Fig. 68, p. 320), An aqueous solution of acetaldehyde is thus obtained. 

Ltease test. The enzyme uretwe hydrolyses urea to ammonium carbonate (p. 519). The reaction is sp ific and is frequently used for solu tions of urea to which the biuret test cannot be applied. Add about 5 drops of phenohred to o 2 g. of urea dissolved in 5 ml. of water. To this yellow solution, add 0 2 g. of jack bean meal suspended in 2 ml. of water containing. also 5 drops of phenol-red. The colour changes to red as the solution becomes alkaline. 

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