Mechanical efficiency

Hydriodic acid. A 1-5 litre three-necked flask is charged with a mixture of 480 g. of iodine and 600 ml. of water. The central aperture is fitted with a stopper carrying an efficient mechanical stirrer leading... 

Dissolve 200 g. of sodium nitrite in 400 ml. of water in a 2-litre beaker provided with an efficient mechanical stirrer, and add 40 g. of copper powder (either the precipitated powder or copper bronze which has been washed with a little ether). Suspend the fluoborate in about 200 ml. of water and add it slowly to the well-stirred mixture. Add 4-5 ml. of ether from time to time to break the froth. The reaction is complete when all the diazonium compound has been added. Transfer the mixture to a large flask and steam distil until no more solid passes over (about 5 litres of distillate). Filter off" the crystalline solid in the steam distillate and dry upon filter paper in the air this o-dinitrobenzene (very pale yellow crystals) has m.p. 116° (t.c., is practically pure) and weighs 29 g. It may be recrystallised from alcohol the recrystallised solid melts at 116-5°. 

In a 2 litre bolt-head flask, equipped with an efficient mechanical stirrer, place 60-5 g. (50 ml.) of pure nitrobenzene and a solution of 30 g. of ammonium chloride in 1 litre of water. Stir vigorously and add 75 g. of a good quality zinc powder (about 90 per cent, purity) in small portions over a period of 5 minutes. The main reaction occurs about 5 minutes after the addition and the temperature rises. When the temperature reaches about 65°, add enough ice to the weU-stirred mixture to reduce the temperature to 50-55°. Filter the solution through a Buchner funnel twenty minutes after the first portion of zinc powder was introduced wash the zinc oxide residues with 600-700 ml. of boiling water. 

Hydrolysis of benzyl cyanide to phenylacetamide. In a 1500 ml. three-necked flask, provided with a thermometer, reflux condenser and efficient mechanical stirrer, place 100 g. (98 ml.) of benzyl]cyanide and 400 ml. of concentrated hydrochloric acid. Immerse the flask in a water bath at 40°. and stir the mixture vigorously the benzyl cyanide passes into solution within 20-40 minutes and the temperature of the reaction mixture rises to about 50°, Continue the stirring for an additional 20-30 minutes after the mixture is homogeneous. Replace the warm water in the bath by tap water at 15°, replace the thermometer by a dropping funnel charged with 400 ml. of cold distilled water, and add the latter with stirring crystals commence to separate after about 50-75 ml. have been introduced. When all the water has been run in, cool the mixture externally with ice water for 30 minutes (1), and collect the crude phenylacetamide by filtration at the pump. Remove traces of phenylacetic acid by stirring the wet sohd for about 30 minutes with two 50 ml. portions of cold water dry the crystals at 50-80°. The yield of phenylacetamide, m.p. 154-155°, is 95 g. RecrystaUisation from benzene or rectified spirit raises the m.p. to 156°. 

Mechanical Pressing. Historically, the first large commercial production of oils from seeds and nuts was carried out using labor-intensive hydraulic presses. These were gradually replaced by more efficient mechanical and screw presses. Solvent extraction was developed for extraction of seeds having low oil content. For seeds and nuts having higher oil content, a combination of a screw press followed by solvent extraction is a common commercial practice (prepress—solvent extraction). 

Oxygen Control. To meet industrial standards for both oxygen content and the allowable metal oxide levels in feed water, nearly complete oxygen removal is required. This can be accompHshed only by efficient mechanical deaeration supplemented by an effective and properly controlled chemical oxygen scavenger. 

In woolen spinning there are no highly efficient mechanical methods to remove VM. Generally, very clean scoured wool, combed wools, or carbonized wool must be used as inputs, or fabrics must be carbonized. 

The lawn-mowing analogy is also interesting in that up to a certain point there will be a linear speedup as mowers are added. This speedup occurs because the mowers do not interfere with each other s work and have efficient mechanisms for coordinating their efforts. The lawn-mowing problem exhibits very good data paraHeHsm. 

To a cold mixture of 800 cc. of 95 per cent ethyl alcohol and 200 cc. of concentrated sulfuric acid (Note i) in a 5-I. round-bottom flask, provided with an efficient mechanical stirrer, is added 250 g. (1.33 moles) of crude 3-bromo-4-aminotoluene (p. 8). The solution is stirred and cooled to 10° and a solution of 148 g. (2.05 moles) of d.s.p. sodium nitrite in 260 cc. of water is added from a separatory funnel. During this addition, the temperature of the mixture must not be allowed to rise above 10°. After all of the nitrite solution has been added, the mixture is stirred twenty minutes longer to complete the diazotization. 

A MIXTURE of 120 g. (3 moles) of sodamide (Note i) and 200 cc. of purified mineral oil (Note 2) is ground together in a mortar until the amide is finely pulverized (Note 3). This suspension is transferred to a 2-I. round-bottom, three-necked flask fitted with a reflux condenser holding a calcium chloride tube, a 500-cc. separatory funnel, and an efficient mechanical stirrer through a mercury seal. The mortar and pestle are rinsed with an additional 250 cc. of the oil which is then added to the reaction flask. This is heated in an oil bath maintained at 160-165, the stirrer is started and 203 g. (i mole) of cyclohexylbromopropene (p. 20) is dropped in during one and one-half hours. Ammonia is evolved and this is allowed to pass through the condenser and is collected in water. 

The reaction mixture should be evenly warmed to 80-90°C within 30 min with efficient mechanical stirring to prevent caking or "hot spots". 

In a 2-1. beaker provided with an efficient mechanical stirrer, 52 g. (0.4 mole) of sodium metaarsenite and 16 g. (0,4 mole) of... 

A. Ethyl N- p-tolylsulfonylmethyl)carhamate,[Carbamic acid, (4 -methyl-phenylsulfonylmethyl)-, ethyl ester]. A solution of 178 g. (1.0 mole) of sodium p-toluenesulfinate (Note 1) in 1 1. of water is placed in a 3-1., three-necked daak, equipped with a condenser, an efficient mechanical stirrer, and a thermometer. After addition of 100 ml. (108 g.) of a 34—37% solution of formaldehyde ca. 1.2-1.4 moles) (Note 2), 107 g. (1.2 moles) of ethyl carbamate (Note 3), and 250 ml. of formic acid (Note 4), the stirred solution is heated to 70°. Soon after this temperature is reached, the reaction mixture becomes turbid by separation of the... 

Heat conduction in the heavy slurry that is formed is poor, and bumping may occur if the mixture is overheated. Efficient mechanical stirring aids this operation. 

Of obvious importance to aircraft is the smoothness of exterior surfaces. Smooth aerodynamic surfaces reduce aerodynamic drag, resulting in higher airspeeds and increased efficiency. Mechanical fasteners, even countersunk flush fasteners, introduce disruptions in the airflow over the exterior surface. Even the slight deformation of thin sheets around fasteners produces drag. Adhesively bonded structure has no fasteners to disrupt airflow and is more capable of producing the smooth continuous contours that are so common on aircraft. 

In a 5-I. round-bottom flask, fitted with an efficient mechanical stirrer and surrounded by an ice-salt mixture, is placed a solution of 121 g. (0.5 mole) of pure dry finely-powdered benzoylperoxide (m.p. 104°) (Note 1) in about 1.51. of dry toluene. The temperature should be below —5°. A solution of sodium ethylate, prepared by dissolving 23 g. (1 mole) of sodium in 500 cc. of absolute alcohol, and cooled to o°, is introduced from a separatory funnel while the mixture is vigorously stirred. This operation should not require more than eight or ten minutes. The liquid whitens and thickens considerably on account of the formation of sodium benzoylperoxide. 

In a 2-1. three-neck, round-bottom flask, fitted with a very efficient mechanical stirrer, a 100-cc. separatory funnel and a large air-cooled reflux condenser (Note 1), the upper part of which is bent downwards and attached to a vertical water condenser, are placed t. jS g. (r.04 moles) of ground diphenylamine (Note 2), 204 g. (1 mole) of iodobenzene, 11. of nitrobenzene (Note 3), 138 g. (1 mole) of finely powdered anhydrous potassium carbonate and 5 g. of copper powder (Note 4). 

The pre-boiler, FW supply should normally be of demineralized quality, such as may be provided by ion exchange, reverse osmosis (RO), or similar process. Extremely efficient mechanical deaeration also is required because the path length from the FW tank to the boiler is usually quite short, and thus the contact time is generally inadequate for the sole use of chemical oxygen scavengers (even catalyzed scavengers). 

Efficient stirring is required. A solution of 225 g. (5.6 moles) of sodium hydroxide in 225 ml. of water can be added to the stirred mixture of the organic substrates in dichloromethane if a more efficient mechanical stirrer is used. In the original procedure, the submitters noted an induction period of about 20 minutes which was stated to vary somewhat with the stirring rate, stirring-bar size, and relative amount of phase-transfer catalyst. Three moles of base are required for the reaction one to generate the carbene and two to react with the additional two moles of hydrochloric acid lost by the amine-carbene adduct in the isonitrile formation step. If less base is used, the excess hydrochloric acid reacts with the isonitrile by a-addition, and the yield is substantially reduced. 

A single-quantum transition involves one spin only, whereas the zero- and doublequantum transitions involve two spins at the same time. The zero- and double-quantum transitions give rise to cross-relaxation pathways, which provide an efficient mechanism for dipole-dipole relaxation. 

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