Heating electrical

The electrical work performed on this system is given by the expressions dWei = Acp dgsys and dwei = IA p dt (Eqs. 3.8.1 and 3.8.3). The portion of the electrical circuit inside the system has an electric resistance given by Re = A(p/1 (Ohm s law). Making the substitution Acp = I Re in the work expressions gives two new expressions for electrical work in this system  

Suppose we redefine the system to be only the liquid. In this case, electric current passes through the resistor but not through the system boundary. There is no electrical work, and we must classify energy transfer between the resistor and the hquid as heat. 

It is easy to operate, has fine temperature control, and is clean, but it is very costly. It needs accessories as transformer, circuit breakers, and cables/bus bars of adequate rating for high currents, instruments such as ammeter, voltmeter, KW and KWH meters, and temperature controller thermostats (to switch on and switch ofif power automatically as per need), or by adjusting the power input by controlling the voltage across the electrodes. 

The efiiciency is high since the heat is generated inside the furnace instead of heat being supplied from outside in case of fuel-oil-fired furnaces. 

There is possibility of mishap when electricity is used for heating (due to short circuit or malfunctioning of thermostat). 

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The collector contains an electrically-heated rubidium salt used as the thermionic source. During the elution of a molecule of a nitrogen compound, the nitrogen is ionized and the collection of these ions produces the signal. The detector is very sensitive but Its efficiency is variable subject to the type of nitrogen molecule, making quantification somewhat delicate. 

This product, given the abbreviation FOD (fuel-oil domestique) in France, still held a considerable market share there of 17 Mt in 1993. However, since 1973 when its consumption reached 37 Mt, FOD has seen its demand shrink gradually owing to development of nuclear energy and electric heating. FOD also faces strong competition with natural gas. Nevertheless, its presence in the French, European and worldwide petroleum balance will still be strong beyond tbe year 2000. 

The basic device is very simple. A tip of refractory metal, such as tungsten, is electrically heat-polished to yield a nearly hemispherical end of about 10" cm radius. A potential of about 10 kV is applied between the tip and a hemispherical fluorescent screen. The field, F, falls off with distance as kr, and if the two radii of curvature are a and b, the total potential difference V is then... 

The acconunodation coefficient for Kr on a carbon filament is determined experimentally as follows. The electrically heated filament at temperature 72 is stretched down the center of a cylindrical cell containing Kr gas at 7. Gas molecules hitting the filament cool it, and to maintain its temperature a resistance heating of Q cal sec cm is needed. Derive from simple gas kinetic theory the expression... 

At constant volumes y" and yt, the state is changed by the adiabatic perfomiance of work (stirring, nibbing, electrical heating ) until the entropy is changed from to S . 

The boron so obtained is an amorphous powder. It can be obtained in the crystalline state by reducing the vapour of boron tribromide with hydrogen, either in an electric arc or in contact with an electrically-heated tungsten filament ... 

The electrically heated type of melting-point apparatus, which has certain advantages over the above types, is described on p. 6i, Fig 33-... 

Concentrate each of the two solutions (or eluates) to about 20 ml, by distilling off the greater part of the benzene, the distilling-flask being immersed in the boiling water-bath. Then pour the concentrated solution into an evaporating-basin, and evaporate the remaining benzene (preferably in a fume-cupboard) in the absence of free flames, i.e., on an electrically heated water-bath, or on a steam-bath directly connected to a steam-pipe. Wash the dry residue from the first eluate with petrol and then dry it in a desiccator pure o-nitroaniline, m.p. 72°, is obtained. Wash the second residue similarly with a small quantity of benzene and dry pure />--nitroaniline, m.p. 148" , is obtained. Record the yield and m.p. of each component. 

The thermostatic mortar P, whose function is described below, is a small electrical heating unit (1 5 cm. in diameter and 7 cm. long) kept constant at 180 . The temperature is kept constant by another Simmerstat. The mortal may be supported on its Simmerstat box or alternatively screwed on to the end of the furnace, a gap of 1 cm. being left between the furnace and the mortar in each case. The right-hand end of the mortar bore is only wide enough to take the drawn-out beak end of the combustion tube, which is thus held in place. 

For temperatures up to 100°, a water bath or steam bath is generally employed. The simplest form is a beaker or an enamelled iron vessel mounted on a suitable stand water is placed in the vessel, which is heated by means of a flame. This arrangement may be used for non-inflammable liquids or for refluxing liquids of low boiling point. Since numerous liquids of low boiling point are highly inflammable, the presence of a naked flame will introduce considerable risk of fire. For such liquids a steam bath or an electrically-heated water bath, provided with a constant-level device, must be used. If the laboratory is equipped with a... 

Ether. The most satisfactory method for the removal of (diethyl) ether is either on a steam bath fed from an external steam supply or by means of an electrically-heated, constant-level water bath (Fig. 77, 5, 1). If neither of these is available, a water bath containing hot water may be used. The hot water should be brought from another part of the laboratory under no circumstances should there be a free flame under the water bath. It caimot be too strongly emphasised that no flame whatsoever may be present in the vicinity of the distillation apparatus a flame 10 feet away may ignite diethyl ether if a continuous bench top lies between the flame and the still and a gentle draught happens to be blowing in the direction of the flame. 

Fig. II, 17, 2 illustrates a fractional distillation unit f for use with glass helices. The column is provided with an electrically-heated jacket the resistance shown in the Figure may be replaced by a variable transformer. The still head is of the total-condensation variable take-off type aU the vapour at the top of the column is condensed, a portion of the condensate is returned to the column by means of the special stopcock (permitting of...

If crystallisation commences as soon as the solvent cools or if large quantities of hot solution are to be filtered, the funnel (and fluted filter paper) should be warmed externally during the filtration (hot water funnel). Three types of hot water funnel are illustrated in Fig. 11,1, 6 no flames should be present whilst inflammable solvents are being filtered through the funnel of Fig. 11, 1, 6, a. Alternatively, the funnel may be surrounded by an electric heating mantle (see Section 11,57) the heat input may be controlled by a variable transformer. When dealing with considerable volumes of aqueous or other solutions which do not deposit crystals rapidly on cooling, a Buchner funnel may be used for filtration (see detailed account in Section 11,1 and Fig. 11 1, 7, c). The filter paper... 

For solids which melt above 100° and are stable at this temperature, drying may be carried out in a steam oven. The crystals from the Buchner funnel should then be placed on a clock glass or in an open dish. The substance may sometimes be dried in the Buchner funnel itself by utilising the device illustrated in Fig. 77, <33, 1. An ordinary Pyrex funnel is inverted over the Buchner funnel and the neck of the funnel heated by means of a broad flame (alternatively, the funnel may be heated by a closely-fltting electric heating mantle) if gentle suction is applied to the Alter flask, hot (or warm) air will pass over the crystalline solid. 

Attention is directed to the fact that ether is highly inflammable and also extremely volatile (b.p. 35°), and great care should be taken that there is no naked flame in the vicinity of the liquid (see Section 11,14). Under no circumstances should ether be distilled over a bare flame, but always from a steam bath or an electrically-heated water bath (Fig.//, 5,1), and with a highly efficient double surface condenser. In the author s laboratory a special lead-covered bench is set aside for distillations with ether and other inflammable solvents. The author s ether still consists of an electrically-heated water bath (Fig. 11, 5, 1), fitted with the usual concentric copper rings two 10-inch double surface condensers (Davies type) are suitably supported on stands with heavy iron bases, and a bent adaptor is fitted to the second condenser furthermost from the water bath. The flask containing the ethereal solution is supported on the water bath, a short fractionating column or a simple bent still head is fitted into the neck of the flask, and the stUl head is connected to the condensers by a cork the recovered ether is collected in a vessel of appropriate size. 

The Stedman-type column is shown in Fig. 11, 56, 25. The characteristic features are (i) the use of a fine stainless steel wire cloth formed into conical discs, and (ii) an accurately fitting Pyrex glass jacket, produced by shrinking Pyrex glass on mandrels to the required inside dimensions. Modifications incorporating a silvered vacuum jacket and an electrically-heated jacket are marketed. This column is said to possess high efficiency but is expensive. It is generally employed in conjunction with a total-condensation variable take-off still head. 

For successful fractional distillation, slow and even heating of the bath surrounding the flask is essential. This may be achieved by suitably designed electrically-heated air baths or by the use of oil baths provided... 

Grind finely pure laboratory grade, anhydrous potassium fluoride, and heat it in an electrically heated oven at 180-210° store in a desiccator. Before use, dry the powdered salt at 180° for 3 hours and grind again in a warm (ca. 50°) glass mortar. 

The silver nitrite may be prepared as described in Section 11,50, 17. The product supplied by Johnson, Matthey and Co. Ltd., of Hatton Garden, London, E.C. 1, is satisfactory it. should be washed with absolute methyl or ethyl alcohol, followed by sodium-dried ether, and dried in an electrically-heated oven at 100 for 30 minutes (longer heating results in darkening on the surface) the substance should be kept in a vacuum desiccator until required. 

Excellent results are obtained by passing acetone vapour over an electrically heated nichrome wire spiral an apparatus, incorporating the latter, is described in the experimental section. 

The best results are obtained with a fractionating column surrounded by an electrically-heated jacket (compare Figs. II, 17. 2. and II. 17, 3), but this is not essential for n-caproic anhydride. For the preparation of propionic or n-biityric anhydride, a highly efficient fiactionating column must be used in order to obtain satisfactory results. 

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