Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Neutral components volatile

Step 3. The neutral components. The ethereal solution (E remaining after the acid extraction of Step 2 should contain only the neutral compounds of Solubility Groups V, VI and VII (see Table XI,5). Dry it with a little anhydrous magnesium sulphate, and distil off the ether. If a residue is obtained, neutral compounds are present in the mixture. Test a portion of this with respect to its solubility in concentrated sulphuric acid if it dissolves in the acid, pour the solution slowly and cautiously into ice water and note whether any compound is recovered. Examine the main residue for homogeneity and if it is a mixture devise procedures, based for example upon differences in volatility, solubility in inert solvents, reaction with hydrolytic and other reagents, to separate the components. [Pg.1096]

Step 4. The steam-volatile neutral compounds. The solution (containing water-soluble neutral compounds obtained in Step 1 is usually very dilute. It is advisable to concentrate it by distillation until about one-third to one-half of the original volume is collected as distillate the process may be repeated if necessary and the progress of the concentration may be followed by determination of the densities of the distillates. It is frequently possible to salt out the neutral components from the concentrated distillate by saturating it with solid potassium carbonate. If a layer of neutral compound makes its appearance, remove it. Treat this upper layer (which usually contains much water) with solid anhydrous potassium carbonate if another aqueous layer forms, separate the upper organic layer and add more anhydrous potassium carbonate to it. Identify the neutral compound. [Pg.1099]

Distillate (S,). This will contain the volatile neutral components present. Concentrate by distillation and saturate with solid KjCOj the neutral component may separate. [Pg.1100]

McNally, M.E. and Grob, R.L. Headspace determination of solubility limits of the base neutral and volatile organic components from the Environmental Protection Agency s list of priority pollutants, J. Chromatogr. A, 284 105-116, 1984. [Pg.1695]

There are few data on concentrations of ethylbenzene in foodstuffs. It has been identified as a trace component in the volatiles from honey, jasmine, papaya, olive oil and cheese flavour and in the neutral component of roast beef flavour isolate (Min et al., 1979 Fishbein, 1985). Trace quantities of ethylbenzene have been detected in split peas (13 ig/kg), lentils (5 ig/kg) and beans (mean, 5 pg /kg maximum 11 pg /kg (Lovegren et al., 1979). Concentrations of ethylbenzene in orange peel (23.6 ng/g dry weight) and in parsley leaves (0.257 pg/g dry weight) have been reported (Goma-Binjul etal., 1996). [Pg.238]

Ether solution. Contains water- insoluble amines. Aqueous solution. Will possess ammo-niacal odour of water-soluble amines present. Distil as long as distillate is alkaline to recover volatile water-soluble amines. the presence of a neutral component. Determine the solubility of a portion in cone. H,S04. Apply any other suitable tests. [Pg.1097]

Distillate (S,). This will contain the volatile neutral components Aqueous alkaline solution. This will contain any acids or phenols present. Cool, acidify (litmus) with dilute H2S04, and add excess of Distillate. ether. Extract with Aqueous alkaline solution (St). Neutralise with dilute HjS04 (Congo red). [Pg.1100]

Distillate. This will contain the steam-volatile acidic and neutral components present. Render alkaline with 10-20 per cent NaOH and distil. Aqueous acid solution (Rt). Render alkaline with 10-20 per cent NaOH and distil. ... [Pg.1296]

Distillate (S,). This will contain the volatile neutral components present. Concentrate by distillation and saturate with solid K2C03 the neutral component may separate. Aqueous alkaline solution. This will contain any acids or phenols present. Cool, acidify (litmus) with dilute H2S04, and add excess of solid NaHC03. Extract with ether. Ether Sodium hydrogen carbonate solution, solution. Acidify with dilute H2S04. Extract Contains with ether. phenolic compounds. Distillate. Extract with ether. Aqueous alkah ne solution (S2). Neutralise with dilute H2S04 (Congo red). Evaporate to dryness and extract with absolute ethanol. The alcoholic extract contains the water-soluble, non-volatile components. [Pg.1296]

Distillate. This wiU contain the steam-volatile acidic and neutral components present. Render alkaline with 10-20% NaOH and distil. [Pg.1100]

Pine and Spruce are the common names used for hundreds of species of conifers belonging to the genus Pinus and Piceay members of the Pinaceae family. Principally, most of these timbers are found in the northern hemisphere. Pine and Spruce species are the source of wood balsam which, after separation of the volatile part (turpentine), yields rosin (colophony). Rosin consists of 90% resin acids an 10% neutral components. [Pg.777]

A fermented-egg product (EEP), patented as an attractive bait for synanthropic flies, has been shown to be attractive to coyotes and repeUent to deer (79). Its components are variable, with relative concentrations of 77% fatty acids, 13% bases, and 10% (primarily) neutrals composed of at least 54 volatiles such as ethyl esters, dimethyl disulfide, and 2-mercaptoethanol. Synthetic formulations have been evaluated to find a replacement for a patented fermented-egg protein product that attracts coyotes and repels deer. Ten aUphatic acids (C-2 to C-8), four amines (pentyl, hexyl, heptyl, and trimethyl), dimethyl disulfide, 2-mercaptoethanol, and 54 more volatiles (C-1 to C-5 esters of C-1 to C-8 acids) have been tested as synthetic fermented egg (SEE) (80) in approximately the same proportions that are present in EEP. Weathering was a problem that caused decreased efficacy, which suggests trials of controUed-release formulations. Eourteen repeUents have been examined against white-taU deer in Peimsylvania in choice tests when treated onto sheUed com (81). [Pg.121]

Dissociation of the neutral acid in water necessitates modifications for air-sea exchange in the model, which is based on Henry s law. Other possible pathways, e.g. sea spray, are neglected. Henry s law is restricted to concentrations of physically solved, non dissociated substances. Since only the non-dissociated acid is volatile, it is important to correct the air-water partition coefficient as to reflect the relative proportions of volatile and non-volatile components. The corrected parameter is the effective Henry s law coefficient, which is related to the Henry s law coefficient as a function of pH (modified Henderson-Hasselbalch equation) ... [Pg.68]

Other sulfonamides. The fact that the extraction of one of these sulfonamides is only optimized at a totally different pH displays the compilations in relying on a single set of extraction conditions as representative for all members within each class of PPCPs. To trap acid components in the sample, the sample has to be acidified to pH < 2, passed through a conditioned column such as an RP C18 solid-phase extraction column, and then eluted with a volatile solvent. Neutral compounds are, on the other hand, extracted by adjusting the sample to pH 7-8 before ranning the sample through the extraction column, which has been conditioned with acetone, methanol, or distilled water. Basic compounds are extracted by initially adjusting the sample to pH > 12 with EDTA and KOH. [Pg.86]

The extracts contained almost pure pheromone, with only minor amounts of other components. By comparison with synthetic samples, derivatization, and gas chromatography on a chiral cyclodextrin phase, the pheromone was identified as a 95 5 mixture of (5)- and (/ )-enantiomers of dimethyl citrate (cupilure (3), Fig. 4.2). Only the (5)-enantiomer was active (Tichy et al., 2001). Cupilure is probably present in ionized form on the silk (pK 3.5), because solvent extracts were neutral. The ionized carboxyl group may be conjugated to basic amino acids of the silk proteins. This would also explain why the pheromone is not volatile, despite its relatively low molecular weight, and is easily washed from the silk by water, including rain. In the tropical habitat of C. salei this would ensure the presence of cupilure only on freshly laid silk. [Pg.127]


See other pages where Neutral components volatile is mentioned: [Pg.1100]    [Pg.83]    [Pg.72]    [Pg.65]    [Pg.87]    [Pg.135]    [Pg.1098]    [Pg.296]    [Pg.3]    [Pg.1098]    [Pg.449]    [Pg.386]    [Pg.90]    [Pg.70]    [Pg.3]    [Pg.196]    [Pg.230]    [Pg.1098]   
See also in sourсe #XX -- [ Pg.187 ]




SEARCH



Neutral components

Volatile component

© 2024 chempedia.info