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Boiling point of the

Another possibility to improve selectivity is to reduce the concentration of monoethanolamine in the reactor by using more than one reactor with intermediate separation of the monoethanolamine. Considering the boiling points of the components given in Table 2.3, then separation by distillation is apparently possible. Unfortunately, repeated distillation operations are likely to be very expensive. Also, there is a market to sell both di- and triethanolamine, even though their value is lower than that of monoethanolamine. Thus, in this case, repeated reaction and separation are probably not justified, and the choice is a single plug-flow reactor. [Pg.51]

The normal boiling points of the materials are given in Table 4.6. Synthesize a continuous reaction, separation, and recycle system for the process, bearing in mind that the process will later become batch. [Pg.118]

TABLE 4.6 Normal Boiling Points of the Components in Example 4.4... [Pg.118]

The heat input to diyers is to a gas and as such takes place over a range of temperatures. Moreover, the gas is heated to a temperature higher than the boiling point of the liquid to be evaporated. The exhaust gases from the dryer will be at a lower temperature than the inlet, but again, the heat available in the exhaust will be available over a range of temperatures. The thermal characteristics of dryers tend to be design-specific and quite difierent in nature from both distillation and evaporation. [Pg.359]

A correlation between retention times and boiling points is established by calibration with a known mixture of hydrocarbons, usually normal paraffins, whose boiling points are known (see Figure 2.2). From this information, the distribution of boiling points of the sample mixture is obtained. [Pg.21]

The TBP (True Bolling Point) distillation gives an almost exact picture of a crude petroieum by measuring the boiling points of the components making up the crude whence its name. [Pg.331]

Figure 2.5 shows the boiling points of the hydrides in elements of Groups IV. V, VI and VII. Clearly there is an attractive force between the molecules of the hydrides of fluorine, oxygen and nitrogen... [Pg.52]

Boron and aluminium halides show many similarities but also surprising differences. Table 7.2 gives the melting and boiling points of the MX3 halides. [Pg.152]

The melting and boiling points of the aluminium halides, in contrast to the boron compounds, are irregular. It might reasonably be expected that aluminium, being a more metallic element than boron, would form an ionic fluoride and indeed the fact that it remains solid until 1564 K. when it sublimes, would tend to confirm this, although it should not be concluded that the fluoride is, therefore, wholly ionic. The crystal structure is such that each aluminium has a coordination number of six, being surrounded by six fluoride ions. [Pg.153]

Assemble the apparatus shown in Fig. 6o. A is a 500 ml. bolt-head flask connected by a knee-tube B to a water-condenser C, to the lower end of which is fitted the adaptor D. In view of the low boiling-point of the ethyl bromide, it is essential that the various portions of the apparatus are connected together by well-bored, tightly fitting corks. (For this reason, the apparatus shown in Fig. 23(0), p. 45, is preferable.)... [Pg.101]

If the thermometer is to be used to determine the elevation of the boiling-point of a liquid on the addition of a solute, it must be remembered that at the boiling-point of the pure solvent the mercury must now be about 1-2 above the bottom of the scale S, and hence for adjustment purposes the temperature of the beaker of water should be 6—7 above the boiling-point of the liquid itself, instead of 1-2 as before. [Pg.430]

The composition of the vapour can easily be calculated as follows — Assuming that the gas laws are applicable, it follows that the number of molecules of each component in the vapour wdll be proportional to its partial pressure, i.e., to the vapour pressure of the pure liquid at that temperature. If and p are the vapour pressures of the two liquids A and B at the boiling point of the mixture, then the total pressure P is given by ... [Pg.13]

Thus for every 6 2 grams of water collectedinthereceiver 10 0 grams of bromobenzene are obtained (or the distillate contains 62 per cent, by weight of bromobenzene) in spite of the fact that bromobenzene has only 119/641 of the vapour pressm of water at the boiling point of the mixture. [Pg.14]

It will be found that the temperature will first rise rapidly until it is near the boiling point of the liquid, then slowly, and finally will remain practically constant. It is a good plan to watch for the ring of condensing vapour in the neck of the flask and to attempt to hold this at... [Pg.84]

When the boiling point of the liquid is above 140-150°, an air condenser (Fig. II, I, 1, c) may replace the water condenser. If the liquid is inflammable, the conical flask may be replaced by a Alter or suction flask (see Fig. II, 1, 7, c), and a length of rubber tubing leading to the sink is attached to the side tubulure. [Pg.85]

If the substance is found to be far too soluble in one solvent and much too insoluble in another solvent to allow of satisfactory recrystallisation, mixed solvents or solvent pairs may frequently be used with excellent results. The two solvents must, of course, be completely miscible. Recrystallisation from mixed solvents is carried out near the boiling point of the solvent. The compound is dissolved in the solvent in which it is very soluble, and the hot solvent, in which the substance is only sparingly soluble, is added cautiously until a slight turbidity is produced. The turbidity is then just cleared by the addition of a small quantity of the first solvent and the mixture is allowed to cool to room temperature crystals will separate. Pairs of liquids which may be used include alcohol and water alcohol and benzene benzene and petroleum ether acetone and petroleum ether glacial acetic acid and water. [Pg.125]

The mono-methyl, ethyl and n-butyl ethers are inexpensive commercial products and are known as methyl carbitol, carbitol and butyl carbitol respectively. They are all completely miscible with water and are purified as already described for the cellosolves (10). The boiling points of the pure compounds are —... [Pg.171]


See other pages where Boiling point of the is mentioned: [Pg.51]    [Pg.119]    [Pg.94]    [Pg.146]    [Pg.513]    [Pg.17]    [Pg.17]    [Pg.117]    [Pg.7]    [Pg.98]    [Pg.102]    [Pg.110]    [Pg.154]    [Pg.267]    [Pg.442]    [Pg.4]    [Pg.8]    [Pg.13]    [Pg.14]    [Pg.15]    [Pg.15]    [Pg.47]    [Pg.85]    [Pg.85]    [Pg.86]    [Pg.86]    [Pg.101]    [Pg.102]    [Pg.102]    [Pg.106]    [Pg.126]    [Pg.145]    [Pg.154]    [Pg.171]   


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Boiling point of the metals

Boiling point of the mixture

Boiling points of the alcohols

Boiling points of the alkanes

Boiling points of the halogens

Boiling points of the noble gases

Boiling, Triple, and Critical Points of the Elements

Determination of the plate number from difference in boiling point

Elevation of the boiling point

Experimental determination of the boiling point

How do dispersion forces determine the boiling point of a substance

Melting, Boiling, Triple, and Critical Point Temperatures of the Elements

Melting, Boiling, Triple, and Critical Points of the Elements

Molecular elevation of the boiling point

Physical Constants of Liquids The Boiling Point and Density

Raising of the Boiling Point

The modification of boiling and freezing points

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