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Concentric mixing

Nitration of 3-phenyl-1,2-benzisoxazole with fuming nitric acid has been shown to give dinitro products of undetermined substitution pattern (67AHC(8)277, p. 290>. However, more satisfactory studies have now been described, especially on the kinetics and mechanism of nitration of 3-methyl-l,2-benzisoxazole (77JCS(P2)47). Nitration in cold, concentrated mixed acids yields the 5-nitro derivative exclusively, nitration in 80-90% sulfuric acid occurring on the free base whereas at higher acidities the conjugate acid is the species involved in the nitration. [Pg.48]

Activities associated with bioreactors include gas/hquid contacting, on-hne sensing of concentrations, mixing, heat transfer, foam control, and feed of nutrients or reagents such as those for pH control. The workhorse of the fermentation industry is the conventional batch fermenter shown in Fig. 24-3. Not shown are ladder rungs inside the vessel, antifoam probe, antifoam system, and sensors (pH, dissolved oxygen, temperature, and the like). Note that coils may lie between baffles and the tank wall or connect to the top to minimize openings... [Pg.2135]

A solution of 44 grams of 2-bromo-4 -benzyloxypropiophenone and 44 grams of 2-(4-meth-oxyphenyDethylamine in 270 ml of ethanol was refluxed for 3 hours. Then the ethanol was distilled off in vacuo and the concentrate mixed with ether. The resulting crystallizate was Sucked off after which the filtrate was mixed with an excess of 2 N hydrochloric acid. As a result of this the hydrochloride of 4 -benzyloxy-2-[2-(4-methoxyphenyl)ethylamino]-propiophenone slowly crystallized. This substance was also Sucked off, washed with water and alcohol, and dried in vacuo. After recrystallization from dilute alcohol the yield was 25.5 grams of a product with a melting point of 217 to 218°C. [Pg.1361]

Column chromatography is the most generally used method, and the use of several different solvents, or graded-concentration mixed solvents affords a considerable selectivity in many cases. The difficulty always remains, however, that an unidentified and unexpected species may accompany one of the carriers and give false results. This can be particularly misleading in cases where the various eluted fractions are not specifically identified, but are classified only by the polarity of the solvent. [Pg.90]

Fig. 4.5.15 Variation of the velocity difference intensity index ( ) and concentration mixing intensity index ( ) with average strain, for bulk droplet volume fraction of 0.4. Lines are shown to guide the eye. Fig. 4.5.15 Variation of the velocity difference intensity index ( ) and concentration mixing intensity index ( ) with average strain, for bulk droplet volume fraction of 0.4. Lines are shown to guide the eye.
The additives can be added during the polymerisation (either in the form of a reactive monomer or as an inert material — advantages include better dispersion and increased retention), but they are usually added immediately postpolymerisation of the polymer and extruded with the polymer. Often a concentrated mix with the plastic (master-batch) is prepared by the plastic manufacturer and this can be sold to the fabricators to be added during subsequent processing. [Pg.88]

Add fresh glutaraldehyde to the peptide/carrier solution to obtain a 1 percent final concentration. Mix well. [Pg.781]

Foam Solution - Fire suppression foam concentrates mixed in proper proportion to water as required by specification of the foam concentrate (currently foam concentrates are available for 1%, 3%, and 6% by water solution mix). [Pg.286]

Most of the asymmetric mixed-matrix membranes reported to date were prepared from concentrated mixed-matrix dopes via a phase inversion technique [69,... [Pg.343]

The goal of reaction monitoring is to optimize reaction conditions such as solvent, reagent ratio, temperature, concentration, mixing method, catalyst and others to push a reaction to completion. These reaction steps include the loading of scaffold, the building block additions, and the final cleavage from the polymer. [Pg.510]

The presence of two methyl groups in m-xylene makes it a more reactive substrate than toluene, but as a consequence, this substrate is more susceptible to oxidation. Therefore, the nitration of m-xylene requires lower temperatures and the use of less concentrated mixed acid. In fact, the nitration of either 2,4- or 2,6-dinitro-m-xylenes to 2,4,6-trinitroxylene (TNX) can be achieved with mixed acid containing up to 10 % water. TNX is a less powerful explosive than TNT and has a poor oxygen balance (—78.4 %). [Pg.135]

Hematological Effects. Hematological effects in a man, apparently exposed to cresol dermally while working with an antiseptic solution containing concentrated mixed cresols, included methemoglobinemia with massive hemolysis and the presence of numerous large Heinz bodies in the blood (Larcan et al. 1974). Similar effects have been reported following oral exposure to cresols (see Section 2.22.2). [Pg.48]

Peuckner adopts a somewhat modified process. Sulphide of sodium is prepared by igniting sulphate of soda with charcoal powder. This is dissolved In water, some free sulphur is added, the liquid Is concentrated, mixed With one half per cent, of sulphate of iron and twenty-five per cent, of a well-tempered day—the purer and whitar the better—the mixture evaporated to dryness, the residue powdered, and ignited for an hour in a cupelling furnace when cold, it is extracted with water, the residue dried, powdered, and once more heated in a muffle, when the required tint appears. [Pg.1073]

The relation between the temperature of nitration and the yield of nitroglycerine is especially marked if less concentrated mixed acids are used. According to Naoum s data, nitrating glycerine in mixed acid containing... [Pg.69]

In the manufacture of high nitrogen guncotton (13.45% N) a more concentrated mixed acid should be used, composed of ... [Pg.378]

A colloidal solution of lead arsenite has been obtained by the following method. A solution of lead acetate is treated with a 10 per cent, solution of sodium lvsalbinate, and after washing the precipitate with hot water, it is dissolved in a dilute aqueous solution of sodium hydroxide containing sodium dihvdrogen arsenite. The liquid, after keeping for some hours, is filtered and dialysed until the outside liquor is free from arsenic. The solution in the dialyser is concentrated, mixed with alcohol and ether, and dried over sulphuric acid in a vacuum. A pale yellow horny mass remains, which dissolves readily in water to form a sol.3... [Pg.170]

Dilute to volume using 80% methanol (see Table 11.6.4 for working concentrations). Mix well by repeated inversion of the flasks. [Pg.1292]

Starting Material. A drum of concentrated, mixed, southern pine kraft black liquor was kindly supplied by the Canton, N. C. mill of the Champion Paper and Fibre Co. Analytical data for the liquor indicated 49.7% total solids and a methoxyl content of the oven-dried solids of 5.54%. The pH of the liquor as received was 12.3. (All melting points are uncorrected. Infrared absorption spectra were determined by Mr. Lowell Sell of The Institute of Paper Chemistry Analytical Group.)... [Pg.161]

Clear indications of the induction period and of an increase in the reaction rate after copolymerization has started were found for isothermal runs by DSC measurements by Peyser and Bascom 941 even for melt copolymerization. According to the copolymerization mechanism, the induction period is interpreted as a gradual increase in the concentration of active centres45,52 and is identical with the time for reaching the maximum on the conductivity curves57). An induction period has also been established by other measurements 39,40>73.90.95), where it is often considered as an imprecision in the determination of the monomer concentration, mixing effect, temperature establishement, or it is not considered at all. [Pg.125]

Add fresh glutaraldehyde to the peptide/carrier solution to obtain a 1% final concentration. Mix well. Caution Use of a fume hood is recommended when working with glutaraldehyde. Avoid contact with skin and clothing. Do not breathe vapors. [Pg.474]

Diphenyl Tellurium Trifluoracetate 8-Quinolinoxide2 A mixture of 1.14 g (10 mmol) trifluoroacetic acid, 5.45 g (10 mmol) diphenyl tellurium dioxinate, and 20 m/ dry benzene is refluxed for 4h. The mixture is concentrated and the concentrate mixed with an excess of diethyl ether to precipitate the product m.p. 170°. [Pg.628]

One of the most attractive features of colloidal semiconductor systems is the ability to control the mean particle size and size distribution by judicious choice of experimental conditions (such as reactant concentration, mixing regimen, reaction temperature, type of stabilizer, solvent composition, pH) during particle synthesis. Over the last decade and a half, innovative chemical [69], colloid chemical [69-72] and electrochemical [73-75] methods have been developed for the preparation of relatively monodispersed ultrasmall semiconductor particles. Such particles (typically <10 nm across [50, 59, 60]) are found to exhibit quantum effects when the particle radius becomes smaller than the Bohr radius of the first exciton state. Under this condition, the wave functions associated with photogenerated charge carriers within the particle (vide infra) are subject to extreme... [Pg.282]

Cobalt Periodate is unknown, but a basic substance corresponding to the formula 7Co0.2l207.18H20 is obtained on concentrating mixed solutions of sodium periodate and cobalt sulphate. It is a yellowish green powder.1... [Pg.47]

Cssium Pentachlor-rhodite, Cs2RhCl 5. H20, is obtained as a beautiful rose-coloured precipitate by concentrating mixed solutions of caesium chloride and potassium pentachlor-rhodite. It is also prepared by concentrating a mixed solution of caesium and rhodium chlorides in the requisite proportions.7... [Pg.163]


See other pages where Concentric mixing is mentioned: [Pg.545]    [Pg.35]    [Pg.2339]    [Pg.159]    [Pg.340]    [Pg.160]    [Pg.1244]    [Pg.184]    [Pg.383]    [Pg.163]    [Pg.101]    [Pg.648]    [Pg.45]    [Pg.197]    [Pg.335]    [Pg.240]    [Pg.565]    [Pg.80]    [Pg.2629]    [Pg.99]    [Pg.112]    [Pg.227]    [Pg.93]   


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Activity coefficients concentrated, mixed salt solutions

Concentrated, Mixed-Salt Solutions

Concentration units mixing ratios

Concentric droplet mixing

Concentric separation-layer mixing

Critical micelle concentration mixed surfactant values

Critical micelle concentration mixed surfactants

Critical micelle concentration mixing

Distribution variables, mixing particle concentration

Flow concentric droplet mixing

Interdigital Concentric Consecutive Mixing

Micropores Concentration Dependence and Predicting Mixed Diffusivities

Mixed layer iron concentrations

Mixed micelles critical micellar concentrations

Mixed micelles critical micelle concentration

Mixed solvent critical micelle concentration

Mixed-function oxidase concentration

Mixing concentrations

Mixing concentrations

Mixing of Concentrated Emulsions

Mixing particle concentration

Mixing process concentrate processing

Mixing process liquid color concentrates

Mixing ratio-concentration relationship

RRR-Tocopherols Concentrate, Mixed

Solid-liquid mixing uniform solids concentrations

Tocopherols Concentrate. Mixed

Units for chemical abundance Concentrations and mixing ratios

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