Cooling advantages

A device that provides additional cooling advantages for the film traveling from the die to the nip rolls, further improving total cooling with the air ring. See nitrogen gas and liquid. 

Scrubbers. Scrubbers are designed to contact a liquid with the particle-laden gas and entrain the particles with the liquid. They offer the obvious advantage that they can be used to remove gaseous as well as particulate pollutants. The gas stream may need to be cooled before entering the scrubber. Some of the more common types of scrubbers are shown in Fig. 11.2. 

Most of the advantages of MCB technology can be used to make small anode-grounded metal-ceramic X-ray tubes as well. These could be water- or air-cooled and reach power ranges up to 1 kW at voltages up to lOOkV. 

For some phenols whose esters are readily hydrolysed, it is advantageous to add the powdered chloride to a pyridine solution of the phenol, warm the mixture on the water-bath for ca. 15 minutes, cool and pour into water, when the sulphonate will separate. 

The advantages of the above air bath are (1) simplicity and cheapness of construction (2)ease of temperature control (3) rapidity of cooling of the contents of the flask effected either by removing the asbestos covers or by completely removing the air bath and (4) the contents of the flask may be inspected by removing the asbestos covers. 

NHjCONHNHj.HCl) and 1-5 g. of crystallised sodium acetate in 10 ml. of water in a test-tube. Add 1 ml. of acetone, close the tube with a cork and shake vigorously. Allow the mixtme to stand, with occasional vigorous shaking, for 10 minutes it is advantageous to cool in ice. FUter the crystals, wash with a httle cold water, and recrystaUise from water or dilute alcohol. The m.p. of acetone semicarbazone is 187°. 

In a 250 ml. conical flask mix a solution of 14 g. of sodium hydroxide in 40 ml. of water and 21 g. (20 ml.) of pure benzaldehyde (Section IV,115). Add 15 g. of hydroxylamine hydrochloride in small portions, and shake the mixture continually (mechanical stirring may be employed with advantage). Some heat is developed and the benzaldehyde eventually disappears. Upon coohiig, a crystalline mass of the sodium derivative separates out. Add sufficient water to form a clear solution, and pass carbon dioxide into the solution until saturated. A colourless emulsion of the a or syn-aldoxime separates. Extract the oxime with ether, dry the extract over anhydrous magnesium or sodium sulphate, and remove the ether on a water bath. Distil the residue under diminished pressure (Fig. 11,20, 1). Collect the pure syn-benzaldoxime (a-benzald-oxime) at 122-124°/12 mm. this gradually solidifies on cooling in ice and melts at 35°. The yield is 12 g. 

Preparation of benzyl cyanide. Place 100 g. of powdered, technical sodium cyanide (97-98 per cent. NaCN) (CAUTION) and 90 ml. of water in a 1 litre round-bottomed flask provided with a reflux condenser. Warm on a water bath until the sodium cyanide dissolves. Add, by means of a separatory funnel fitted into the top of the condenser with a grooved cork, a solution of 200 g. (181-5 ml.) of benzyl chloride (Section IV.22) in 200 g. of rectified spirit during 30-45 minutes. Heat the mixture in a water bath for 4 hours, cool, and filter off the precipitated sodium chloride with suction wash with a little alcohol. Distil off as much as possible of the alcohol on a water bath (wrap the flask in a cloth) (Fig. II, 13, 3). Cool the residual liquid, filter if necessary, and separate the layer of crude benzyl cyanide. (Sometimes it is advantageous to extract the nitrile with ether or benzene.) Dry over a little anhydrous magnesium sulphate, and distil under diminished pressure from a Claisen flask, preferably with a fractionating side arm (Figs. II, 24, 2-5). Collect the benzyl cyanide at 102-103°/10 mm. The yield is 160 g. 

Electrolysis cell. This is shown in Fig. VI, 31, 1 and is almost self-explanatory. The cylindrical cell of Pyrex glass (6" long by 2 " diameter) is cooled by immersion in a cooling bath. The electrodes consist of two platinum plates (4 cm. X 2-5 cm. X 0-3 mm.), which are placed about 2 mm. apart. The temperature of the electrolyte is maintained at 30-35° by means of the internal cooling coil and also by immersion of the cell in ice-water. A current of 1 5-2 0 amperes is passed until the electrolyte becomes slightly alkaline, which normally takes about 20-50 per cent, longer than the calculated time on the basis of the current and the amounts of acid employed. It is advantageous to reverse the direction of the current occasionally. 

The following alternative procedure is recommended and it possesses the advantage that the same tube may be used for many sodium fusions. Support a Pyrex test tube (150 X 12 mm.) vertically in a clamp lined with asbestos cloth or with sheet cork. Place a cube (ca. 4 mm. side = 0 04 g.) of freshly cut sodium in the tube and heat the latter imtil the sodium vapour rises 4 5 cm. in the test-tube. Drop a small amount (about 0-05 g.) of the substance, preferably portionwise, directly into the sodium vapour CAUTION there may be a slight explosion) then heat the tube to redness for about 1 minute. Allow the test tube to cool, add 3-4 ml. of methyl alcohol to decompose any unreacted sodium, then halffill the tube with distilled water and boil gently for a few minutes. Filter and use the clear, colourless filtrate for the various tests detailed below. Keep the test-tube for sodium fusions it will usually become discoloured and should be cleaned from time to time with a little scouring powder. 

A recently developed drying appHcation for zeoHtes is the prevention of corrosion in mufflers (52,55). Internal corrosion in mufflers is caused primarily by the condensation of water and acid as the system cools. A unique UOP zeoHte adsorption system takes advantage of the natural thermal cycling of an automotive exhaust system to desorb the water and acid precursors. 

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