Distillate, definition

Naphtha, heavy hydrotreated. See Naphtha, hydrotreated heavy Naphtha, hydrodesulfurized heavy CAS 64742-82-1 EINECS/ELINCS 265-185-4 Synonyms High flash white spirit Hydrodesulfurized heavy naphtha Hydrodesulfurized naphtha, heavy Naphtha (petroleum), hydrodesulfurized heavy Petroleum naphtha, hydrodesulfurized heavy White spirits, hydrodesulfurized White spirit. White spirit, high flash Classification Petroleum distillate Definition Complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process mixt. of aliphatic and aromatic hydrocarbons, predominantly C7-12 Properties B.p. 90-230 C Uses Solvent... 

Naphtha, aromatic, high flash Solvent naphtha (petroleum), light aromatic Ciassification Petroleum distillate Definition Complex combination of hydrocarbons obtained from distillation of aromatic streams consists of predominantly C8-10 aromatic hydrocarbons... 

Classification Petroleum distillate Definition Complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process consists of hydrocarbons in C11-20 range, boiling range 205-345 C Properties B.p. 205-345 C Toxicology OSHA PEL 5 mg/m ... 

CAS 64742-52-5 EINECS/ELINCS 265-155-0 Synonyms Distillates (petroleum), hydroteated (mild) heavy naphthenic Distillates (petroleum), hydrotreated heavy naphthenic Hydrotreated heavy naphthenic distillate Hydrotreated (mild) heavy naphthenic distillate Mineral oil, petroleum distillates, hydrotreated (mild) heavy naphthenic Petroleum distillates, hydrotreated (mild) heavy naphthenic Ciassification Petroleum distillate Definition Complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst consists of predominantly C20-50 hydrocarbons contains relatively few normal paraffins Properties B.p. 350 C... 

Classification Sat. aliphatic hydrocarbon petroleum distillate Definition Complex combination of hydrocarbons obtained by treating a petrol, fraction with hydrogen in presence of a catalyst consists of hydrocarbons in C11-25 range, boiling range 205400 C... 

Distillation under Reduced Pressure. Occasionally a liquid, when distillation is attempted under atmospheric pressure, will undergo partial or complete decomposition before its boiling-point is reached. To overcome this difficulty, the liquid is distilled under reduced pressure, so that its boiling-point shall be definitely below its thermal decomposition point. 

The residual liquid in the flask is a dilute alkaline solution of sodium acetate. To liberate the acetic acid, add dilute sulphuric acid until the solution is definitely acid to litmus, and then distil off about 20 ml. Perform on this aqueous distillate the tests for acetic acid given on p. 347-... 

Add dil. HjS04 to the residue in the flask until definitely acid to litmus. Distil off 1 2 ml., and perform tests on this aqueous distillate for acetic acid. 

Take two test-tubes A and B in A place about 5 ml. of neutralised tartaric acid solution and in B place 5 ml. of distilled water. To each solution add 3-4 drops of ferric chloride solution. Place a piece of white paper under the tubes, look down their length and note that A is definitely yellow compared with the control tube B. This yellow colour is given by a-hydroxy-carboxylic-acids, lactic acid, tartaric acid, citric acid. 

Oxidation, (i) Dissolve 5 g. of potassium dichromate in 20 ml. of dil. H2SO4 in a 100 ml. bolt-head flask. Cool and add 1 ml. of methanol. Fit the flask with a reflux water-condenser and warm gently a vigorous reaction soon occurs and the solution turns green. The characteristic pungent odour of formaldehyde is usually detected at this stage. Continue to heat for 3 minutes and then fit the flask with a knee-tube (Fig. 59, p. 100) and distil off a few ml. Test the distillate with blue litmus-paper to show that it is definitely acid. Then apply Test 3 p. 350) for formic acid. (The reflux-distillation apparatus (Fig. 38, p. 63) can conveniently be used for this test.)... 

If a phenol is not indicated, the solution may contain an aliphatic acid. Transfer to a distilling-flask, make definitely acid with dih H2SO4, and distil the volatile formic and acetic acids if present will distil over. If the distillation gives negative reactions, test the residual solution in the flask for oxalic, succinic, lactic, tartaric and citric acids and glycine, remembering that the solution is strongly acid. 

To the cold acid chloride add 175 ml. of pure carbon disulphide, cool in ice, add 30 g, of powdered anhydrous aluminium chloride in one lot, and immediately attach a reflux condenser. When the evolution of hydrogen chloride ceases (about 5 minutes), slowly warm the mixture to the boiling point on a water bath. Reflux for 10 minutes with frequent shaking the reaction is then complete. Cool the reaction mixture to 0°, and decompose the aluminium complex by the cautious addition, with shaking, of 100 g. of crushed ice. Then add 25 ml. of concentrated hydrochloric acid, transfer to a 2 htre round-bottomed flask and steam distil, preferably in the apparatus, depicted in Fig. II, 41, 3 since the a-tetralone is only moderately volatile in steam. The carbon disulphide passes over first, then there is a definite break in the distillation, after whieh the a-tetralone distils completely in about 2 htres of distillate. 

The distillate may contain volatile neutral compounds as well as volatile acids and phenols. Add a slight excess of 10-20 per cent, sodium hydroxide solution to this distillate and distil until the liquid passes over clear or has the density of pure water. The presence of a volatile, water-soluble neutral compound is detected by a periodic determination of the density (see Section XI,2) if the density is definitely less than unity, the presence of a neutral compound may be assumed. Keep this solution Si) for Step 4. 

The oil that remains is only slightly dark. Definitely translucent which is always lovely. One can then add some water to take up the unreacted salts and separate the oil from this. If an emulsion forms it can be busted up with some 10% HCl. That isosafrole is clean enough to proceed with but it can of course be distilled for ultra purity. 

Exceptions to the simple definition of an essential oil are, for example, gadic oil, onion oil, mustard oil, or sweet birch oils, each of which requires enzymatic release of the volatile components before steam distillation. In addition, the physical process of expression, appHed mostly to citms fmits such as orange, lemon, and lime, yields oils that contain from 2—15% nonvolatile material. Some flowers or resinoids obtained by solvent extraction often contain only a small portion of volatile oil, but nevertheless are called essential oils. Several oils are dry-distiUed and also contain a limited amount of volatiles nonetheless they also are labeled essential oils, eg, labdanum oil and balsam oil Pern. The yield of essential oils from plants varies widely. Eor example, nutmegs yield 10—12 wt % of oil, whereas onions yield less than 0.1% after enzymatic development. 

Oakmoss. Extracts of oakmoss are extensively used in perfumery to furnisli parts of the notes of the fougnre or chypre type. The first step in the preparation of an oakmoss extract is treatment of the Hchen Evemiaprunastri (L.) Ach., collected from oak trees mainly in southern and central Europe, with a hydrocarbon solvent to obtain a concrete. The concrete is then further processed by solvent extraction or distillation to more usable products, of which absolutes are the most versatile for perfumery use. A definitive analysis of oakmoss volatiles was performed in 1975 (52). The principal constituents of a Yugoslav oakmoss are shown in Table 15 (53). A number of phenoHc compounds are responsible for the total odor impression. Of these, methyl P-orcinol carboxylate is the most characteristic of oakmoss. 

When this is combined with the definition of minimum separation work, an approximation for distillation efficiency for an ideal binary can be obtained ... 

In the fire codes, the atmospheric boiling point is an important physical property used to classify the degree of hazardousness of a Hquid. If a mixture of Hquids is heated, it starts to bod at some temperature but continues to rise ia temperature over a boiling temperature range. Because the mixture does not have a definite boiling poiat, the NFPA fire codes define a comparable value of boiling poiat for the purposes of classifying Hquids. For petroleum mixture, it is based on the 10% poiat of a distillation performed ia accordance with ASTM D86, Standard Method of Test for Distillation of Petroleum Products. 

Most distillation systems ia commercial columns have Murphree plate efficiencies of 70% or higher. Lower efficiencies are found under system conditions of a high slope of the equiHbrium curve (Fig. lb), of high Hquid viscosity, and of large molecules having characteristically low diffusion coefficients. FiaaHy, most experimental efficiencies have been for biaary systems where by definition the efficiency of one component is equal to that of the other component. For multicomponent systems it is possible for each component to have a different efficiency. Practice has been to use a pseudo-biaary approach involving the two key components. However, a theory for multicomponent efficiency prediction has been developed (66,67) and is amenable to computational analysis. 

When simple Hquids like naphtha are cracked, it may be possible to determine the feed components by gas chromatography combined with mass spectrometry (gc/ms) (30). However, when gas oil is cracked, complete analysis of the feed may not be possible. Therefore, some simple definitions are used to characterize the feed. When available, paraffins, olefins, naphthenes, and aromatics (PONA) content serves as a key property. When PONA is not available, the Bureau of Mines Correlation Index (BMCI) is used. Other properties like specific gravity, ASTM distillation, viscosity, refractive index. Conradson Carbon, and Bromine Number are also used to characterize the feed. In recent years even nuclear magnetic resonance spectroscopy has been... 

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