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Simple distillation normal boiling

It must be borne in mind that in spite of the fact that the solvents have normal boiling points below 90-95°, they cannot always be completely removed by heating on a steam or water bath when they form part of mixtures with less-volatile liquids. Simple distillation may lead to mixtures with higher boiling points than the individual solvents, so that separation of the latter may not be quite complete. In such cases the distillation should be completed with the aid of an air bath (Fig. 77,5,3) or an oil bath the Are hazard is considerably reduced since most of the solvent will have been removed. [Pg.90]

Another type of problem may also arise from the formation of azeotropes, w ose boiling points are close to that of isoprene. This is the case of cydopentadiene, whose separation, like that of piperylene, should normally take place by simple distillation, but wUch produces azeotropes with n-pentane (35J Q, 2butenes (38 Q and ds 2-pentene (36,9 C). [Pg.229]

The overproduction of ethylene in certain geographic areas and, all things considered, the strong demand for acetylene at its high price level, could normally justify its recovery from the steam-cracked C3 cut for economic reasons. Given the slight differences in boiling points between the constituents of these effluents, and the pronounced tendency displayed by acetylenic compounds lo polymerize, this separation cannot be achieved by simple distillation or even superfractionation. A feasible alternative is solvent extraction, particularly with dimethylform amide. [Pg.322]

For the development of the separation section we will examine the composition and the thermodynamic behaviour of the outgoing reaction mixture. This contains benzene, ethylbenzene and poly ethylbenzenes. The separation sequencing is simple because the mixture is zeotropic and the difference in the normal boiling points of components is large. A first distillation column takes off benzene for recycle, a second one separates... [Pg.339]

As in the case of azeotropic distillation, there is the problem of separating the solvent from the product, but for extractive distillation the problem is much simpler, since the solvent is normally tpiite high boiling, beyond the range of azeotrope formation, and simple distillation usually is sufficient to separate the solvent for reuse. [Pg.264]

Azeotropic (or zeotropic) components cannot be separated in simple multistage distillation processes, or generally by addition of "spedal" components. In other words, the azeotrope can t be "broken" or "unlocked." The noun "broken" is conventionally used to mean that the azeotropic components can be separated by simple multistage distillation that the components of the "broken" azeotropic blend display the normal boiling points and individual HSP values of each component None of that is so/... [Pg.164]

Steam distillation is used when normal distillation is not an option, due to thermal sensitivities. By adding water or steam, the boiling points of compounds can be depressed, allowing them to evaporate at lower temperatures. After distillation the vapours are condensed and typically yield two phases water and organics. These can then be easily separated on the basis of their different densities. On a simple level, this can be seen every day in fresh black coffee, where small amounts of organic, water-immiscible oils float on the surface. Steam distillation is employed on an industrial scale in the manufacture of essential oils (e.g. lavender, eucalyptus and fruit oils) that are used in the food and flavour industries. In this area, the use of water is highly desirable as a natural solvent. Steam distillation is also used in petroleum refineries and petrochemical plants, where it is commonly referred to as steam stripping . [Pg.49]

Lead triethyl, EtsPb.-Sixty-five grams of lead triethyl chloride, covered with 100 c.c. of distilled water, are treated with 40 c.c. of 5-Normal sodium hydroxide and the mixture stirred until solution is complete. Addition of 200 c.c. of 5-Normal sodium hydroxide precipitates the lead triethyl hydroxide, which is separated. Sixty grams of the latter in 200 c.c. of 95 per cent, alcohol are electrolysed with lead electrodes, using a current density of 0-01 amperes per sq. cm. Lead triethyl forms as an oil at the cathode. It is pale yellow in colour, density 1 94, and readily oxidised in air, giving a yellowish powder. It may be distilled in steam, and at 2 mm. pressure it boils at 100° C., but it decomposes when distilled at ordinary pressure. It is still liquid at C. In dilute solution it corresponds to the simple formula,... [Pg.339]

The advantages of continuous distillation are particularly clear for binaiy mixtures of components having a large difference in boiling point. The apparatus can then be relatively simple and can run for days on end without interruption even in glass equipment a considerable throughput can be obtained, both at normal and reduced pressures. By the use of a second column, ternary mixtures can also be... [Pg.248]


See other pages where Simple distillation normal boiling is mentioned: [Pg.24]    [Pg.34]    [Pg.49]    [Pg.219]    [Pg.322]    [Pg.57]    [Pg.12]    [Pg.219]    [Pg.239]    [Pg.259]    [Pg.753]    [Pg.313]    [Pg.164]    [Pg.1313]    [Pg.396]    [Pg.323]    [Pg.1136]    [Pg.59]    [Pg.419]    [Pg.266]    [Pg.718]    [Pg.300]    [Pg.201]   


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