Swirls

Eddy Currents ttike their name from the swirls (eddies) observed in turbulent water flow. The Greek mythology tells us about Charybdis. A monster eddy current between Italy and Sicily whose attractive field pulled unwary sailors to their destruction. Our kind of eddy currents are usually not so dangerous, they flow in electrical conductors and are a branch of Electromagnetics. Where does that spring from Could it make eddy currents the very oldest NDT technique ... 

Flartree D R, Flartree W and Swirles B 1940 Self-oonsistent field inoluding exohange and superposition of oonfigurations with some results for oxygen Phil. Trans. R. See. A 238 229-47 The work of Fook is given in ... 

Place 100 g. of adipic acid in a 750 ml. round-bottomed flask and add successively 100 g. (127 ml.) of absolute ethyl alcohol, 250 ml. of sodium-dried benzene and 40 g. (22 ml.) of concentrated sulphuric acid (the last-named cautiously and with gentle swirling of the contents of the flask). Attach a reflux condenser and reflux the mixture gently for 5-6 hours. Pour the reaction mixture into excess of water (2-3 volumes), separate the benzene layer (1), wash it with saturated sodium bicarbonate solution until eflfervescence ceases, then with water, and dry with anhydrous magnesium or calcium sulphate. Remove most of the benzene by distillation under normal pressure until the temperature rises to 100° using the apparatus of Fig. II, 13, 4 but substituting a 250 ml. Claisen flask for the distilling flask then distil under reduced pressure and collect the ethyl adipate at 134-135°/17 mm. The yield is 130 g. 

Dissolve 180 g. of commercial ammonium carbonate in 150 ml. of warm water (40-50°) in a 700 ml. flask. Cool to room temperature and add 200 ml. of concentrated ammonia solution (sp. gr. 0 88). Introduce slowly, with swirling of the contents of the flask, a solution of 50 g. of chloroacetic acid (Section 111,125) in 50 ml. of water [CAUTION do not allow chloroacetic acid to come into contact with the skin as unpleasant burns will result]. Close the flask with a solid rubber stopper and fix a thin copper wire to hold the stopper in place do not moisten the portion of the stopper in contact with the glass as this lubrication will cause the stopper to slide out of the flask. Allow the flask to stand for 24-48 hours at room temperature. Transfer the mixture to a distilling flask and distil in a closed apparatus until the volume is reduced to 100-110 ml. A convenient arrangement is to insert a drawn-out capillary tube into the flask, attach a Liebig s condenser, the lower end of which fits into a filter flask (compare Fig.//, 1) and connect the... 

Dissolve 10 g. of sym.-tribromoaniline (Section IV,47) in 60 ml. of rectified spirit and 15 ml. of benzene in a 200 ml. bolt-head flask by heat ing on a water bath. Add, from a burette or small graduated pipette, 5-3 g. (3-5 ml.) of concentrated sulphuric acid to the hot solution and gently swirl the liquid. Attach a reflux condenser to the flask and heat on a water bath until the clear solution boils. Detach the condenser, remove the flask from the water bath, and add 3 5 g. of powdered sodium... 

To determine the exact peroxide content of benzoyl peroxide (and of other organic peroxides) the following procedure may be employed. Place about 0 05 g. of the sample of peroxide in a glass-stoppered conical flask add 5-10 ml. of acetic anhydride (A.R. or other pure grade) and 1 g. of powdered sodium iodide. Swirl the mixture to dissolve the sodium iodide and allow the solution to stand for 5-20 minutes. Add 50-75 ml. of water, shake the mixture vigorously for about 30 seconds, and titrate the liberated iodine with standard sodium thiosulphate solution using starch as indicator. 

In a 1-litre round-bottomed flask, fitted with a condenser and trap (compare Fig. II, 13, 8), place 62 g. (61 ml.) of aniline. Cool the flask in an ice bath, add 120 ml. of concentrated hydrochloric acid slowly, followed by 90 g. of paraldehyde swirl the contents of the flask to ensure thorough mixing. Remove the flask from the ice bath and shake it frequently at... 

Dissolve 14 g. of p-phenetidine (2) in 240 ml. of water to which 20 ml. of 5N hydrochloric acid (or 9 ml. of the concentrated acid) have been added stir the solution with about 5 g. of decolourising carbon for 5 minutes, warm, and filter the solution with suction. Transfer the cold filtered solution of p-phenetidine hydrochloride to a 700 ml. conical flask, add 13 g. (12 ml.) of acetic anhydride and swirl the contents to dissolve the anhydride. Immediately add a solution of 16 g. of crystallised sodium acetate in 50 ml. of water and stir (or swirl) the contents of the flask vigorously. Cool the reaction mixture in an ice bath, filter with suction and wash with cold water. RecrystaUise from hot water (with the addition of a little decolourising carbon, if necessary), filter and dry. The yield of pure phenacetin, m.p. 137°, is 12 g. 

The reaction may be more easily controlled and the chlorosulphonic acid added all at once if the acetanilide is employed in the form of a hard cake. The latter is prepared by melting the acetanilide in the flask over a free flame and causing the compound to solidify over the lower part of the flask by swirling the liquid. If the reaction becomes too vigorous under these conditions, cool the flask momentarily by immersion in an ice bath. 

The next day comes and the hung-over chemist wakens to see a dark red solution stirring away. In some cases where the chemist had made an enormous batch of this stuff, there may be seen a small mass of crystalline precipitate at the bottom of the flask. This is no big deal and will go away in the next step. If the chemist had made this in a flat-bottomed flask (which she really should have for convenience) then the ice tray is removed, the flask returned to the stir plate, a distillation setup attached, and the acetone is vacuum distilled from the flask. After all the acetone has come over the chemist can proceed in two different ways. One way is to just keep on distilling the solution until all of the formic acid has been removed. The chemist knows that just about all the formic has been removed when there is about 300mL of thick black liquid remaining in the reaction flask and hardly any clear formic acid is dripping over into the collection flask. If one were to swirl the reaction flask, the liquid will appear syrupy and kind of coat the sides of the flask. This is more evident when the flask cools. A quick sniff of the flask may indicate that some formic is still in there, but it should be too minimal to be of any concern. 

To clean the white residue off of your glassware, dump some muriatic acid straight from the jug onto them and swirl. 

Apparatus 2-1 flask, see Fig. 2 (note 1). Instead of mechanical stirring occasional swirling by hand may be applied a one-necked flask provided with a stopper with a small hole can also be used. 

Before starting the preparation, one should perform the following test. Add a very small piece of the metal if after about 2 min (continuous swirling or stirring) the blue colour has disappeared, introduce a second piece. Repeat this procedure until the blue colour persists. 

Note 7. To a solution of 0.55 mol of sodium hydroxide in 150 ml of methanol and 40 ml of water was added a cold solution of 0.55 mol of methanethiol in 50 ml of methanol with cooling below 10°C. Subsequently 0.50 mol of propargyl chloride was added with swirling in 15 min, while keeping the temperature between 20 and 40°C. After an additional 30 min 1 1 of water was added and the product was extracted six times with small amounts of pentane. The extracts were washed with water, dried and the solvent was... 

In 400 ml of anhydrous liquid ammonia (note 1) (drawn from a cylinder) in the 3-1 flask were dissolved 25 g of K0-tert.-Ci,tig (see Exp. 4, note 2). 1,4-Dimethoxy--2-butyne (Chapter VIII-6, Exp. 8) (0.60 mol) was poured into the solution. The reaction mixture was allowed to stand (with occasional swirling) for 25 min, after which 50 g of powdered ammonium chloride were introduced in 5 min with manual swirling. The ammonia was driven off by placing the flask in a water bath at 40 C. 

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