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Solvent continued production

Continuous processes have been developed for the alcohols, operating under pressure with Hquid ammonia as solvent. Potassium hydroxide (206) or anion exchange resins (207) are suitable catalysts. However, the relatively small manufacturing volumes militate against continuous production. For a while a continuous catalytic plant operated in Raveima, Italy, designed to produce about 40,000 t/yr of methylbutynol for conversion to isoprene (208,209). [Pg.114]

Stabilizers, pigments, and other additives are milled in spinning solvent, normally along with small amounts of the urethane polymer to improve dispersion stabiUty this dispersion is then blended to the desired concentration with polymer solution after chain extension. Most producers combine prepolymerization, chain extension, and additive addition and blending into a single integrated continuous production line. [Pg.307]

Vapor-phase catalytic oxidation of dutene is a mote direct route to the dianhydtide. Hbls in Europe apparently uses this route, which eliminates the need for a separate dehydration step and for handling of any oxidants or solvents. Continuous operation is faciHtated, corrosion is minimized, and product recovery is simplified. The vapor-phase oxidation of dutene is similar to that of o-xylene to phthaHc anhydtide, and phthaHc anhydtide units can be... [Pg.499]

Figure 2.5 Possible technological solutions to bioprocess problems a) Fed-batch culture b) Continuous product removal (eg dialysis, vacuum fermentation, solvent extraction, ion exchange etc) c) Two-phase system combined with extractive fermentation (liquid-impelled loop reactor) d) Continuous culture, internal multi-stage reactor e) Continuous culture, dual-stream multi-stage reactor f) Continuous culture with biomass feedback (cell recycling). (See text for further details). Figure 2.5 Possible technological solutions to bioprocess problems a) Fed-batch culture b) Continuous product removal (eg dialysis, vacuum fermentation, solvent extraction, ion exchange etc) c) Two-phase system combined with extractive fermentation (liquid-impelled loop reactor) d) Continuous culture, internal multi-stage reactor e) Continuous culture, dual-stream multi-stage reactor f) Continuous culture with biomass feedback (cell recycling). (See text for further details).
Qureshi, N., and Maddox, I. S., A Mathematical Model of a Fluidized Bed Reactor for the Continuous Production of Solvents by Immobilized Clostridium acetobutylicum, J. Chem. Tech. Biotechnol., 48 369 (1990)... [Pg.675]

The ethylene resides in the reactor about two minutes, and as it polymerizes, it remains dissolved in the cyclohexane. To keep the concentration of polyethylene in the cyclohexane at 35-40%, a solution of the feed, solvent, and product are continuously drawn off. Downstream, the ethylene flashes off to be recycled in a flash tower. A precipitator removes the polyethylene from the cyclohexane by centrifuge. The polyethylene is steam-stripped to remove any remaining cyclohexane, then dried, extruded, pelletized, and packaged. [Pg.341]

Pilot plant operations, as we have noted previously, can vary between extremes of flow rates. It is necessary, therefore, that the feed and reagent volumes be large enough that the pilot plant may be operated for a sufficient length of time to obtain meaningful data. For example, if the aqueous feed to the solvent extraction (SX) circuit is being produced batchwise, variations between batches are bound to occur. Such variations should be controlled as much as possible. Batchwise production of the feed solution may be very different from feed to the actual plant, especially if the plant process involves continuous production of the feed to the SX circuit. [Pg.304]

Hydrogen peroxide is commercially produced by autooxidation of ethyl anthraquinol in a solvent such as toluene or ethylbenzene. The product ethyl anthraquinone is reduced by hydrogen over supported nickel or platinum catalyst to regenerate hack the starting material, ethyl anthraquinol for a continuous production of H2O2. The reaction steps are ... [Pg.373]

All these methods provide different possibilities regarding throughput, temperature, pressure, etc. While non-sealed reactors have the simplest production setup, they are limited in the possible reaction temperature to the boiling point of the solvent, e.g. 100 °C for water. In contrast, autoclaves allow much higher reaction temperatures. An extruder system is especially useful for products with higher viscosity and provides all the advantages of a continuous production process rather than batchwise manufacturing. [Pg.463]

The preparation of some (S)-alcohols by ADH from Rhodococcus erythro-polis has been described quite recently. This was the first report of a continuous production process for hydrophobic compounds. An important prerequisite of this method is a membrane which is resistant to organic solvents. It separates the hydrophilic phase, which contains the enzyme and the coenzyme, from the hydrophobic phase with the substrate and the product. Several products were prepared with this enzyme at a multigram scale (Table 16). [Pg.178]

In the process, anhydrous formaldehyde is continuously fed to a reactor containing well-agitated inert solvent, especially a hydrocarbon, in which monomer is sparingly soluble. Initiator, especially amine, and chain-transfer agent are also fed to the reactor. The reaction is quite exothermic and polymerization temperature is maintained below 75°C (typically near 40°C) by evaporation of the solvent. The product polymer is not soluble in the solvent and precipitates early in the reaction. [Pg.7]

There has been considerable effort directed toward the immobilization of both enzymes and whole cells in a wide array of formats.15 Initial attempts to immobilize enzymes on naturally derived supports such as charcoal were conducted early in the twentieth century and eventually led to the development of more robust biocatalysts immobilized on synthetic resins by the mid-1950s. Immobilization often confers a number of advantages relative to the free biocatalyst including ease of removal from the process stream, potential for reuse, improvements in stability, favorable alterations in kinetic parameters, suitability for continuous production and in some cases the ability to operate in organic solvents. The focus of this section is on the immobilization of enzymes, however, many of the same principles apply to whole cells, the primary difference being the fact that immobilized cells are often less stable than individual enzymes and may contain additional undesired enzyme activities. [Pg.1392]

Secondary metabolites produced by plant cell culture are commonly accumulated in the cells. With few exceptions such as Capsicum frutescens, Thalictrum minus (9) and Vanilla planifolia (Knorr, D. and Romagnoli, L., Univ. of Delaware, unpublished data) cultures, which release valuable compounds such as capsaicin, berberine and vanillin, respectively, into the medium, procedures to induce product release are required to develop continuous production processes. Reported permeabilization methods include treatment with dimethylsulfoxide (DMSO), isopropanol, toluene, phenethyl alcohol or chloroform (9, 28). But as Fontanel and Tabata (9) pointed out, such treatments with organic solvents are severe and other methods of permeabilization need to be developed. [Pg.72]

Products formed in plant cells are usually intracellular storage products and must therefore be released from the cells if the product is to be continuously collected in the medium. This is especially important in immobilized cell systems. There are several environmental factors that will allow for release of products such as modifications in the media pH (35) and addition of solvents that permeabilize the cells Q, 36). It has also been demonstrated that operation in two-phase reactors, where the products are extracted into the nonaqueous phase, can be effective. Both liquid-liquid (37) and liquid-solid (38) systems have been used. The continuous release of products in this manner would also favor their continuous production since the storage capacity of the cells would not become limiting. [Pg.194]

Summary TATB is easily prepared by ammoniating trichlorotrinitrobenzene in benzene solvent. The product TATB immediately precipitates upon the addition of the ammonia gas, and continues through out the ammonia addition. After the addition is complete, the product is then filtered-off, washed and dried. Commercial Industrial note For related, or similar information, see Serial No. 813,039, May 13th, 1959, by The United States Navy, to Lloyd A. Kaplan, Adelphi, MD, and Francis Taylor, Jr., Baltimore MD. Part or parts of this laboratory process may be protected by international, and/or commercial/industrial processes. Before using this process to legally manufacture the mentioned explosive, with intent to sell, consult any protected commercial or industrial processes related to, similar to, or additional to, the process discussed in this procedure. This process may be used to legally prepare the mentioned explosive for laboratory, educational, or research purposes. [Pg.162]

Continuous homogeneous catalysis is achieved by membrane filtration, which separates the polymeric catalyst from low molecular weight solvent and products. Hydrogenation of 1-pentene with the soluble pofymer-attached Wilkinson catalyst affords n-pentane in quantitative yield A variety of other catalysts have been attached to functionalized polystyrenes Besides linear polystyrenes, poly(ethylene glycol)s, polyvinylpyrrolidinones and poly(vinyl chloride)s have been used for the liquid-phase catalysis. Instead of membrane filtration for separating the polymer-bound catalyst, selective precipitation has been found to be very effective. In all... [Pg.79]

Interest in the photochemistry of the phthalimide systems has continued. The phthalimide derivatives (316) are phot ochemically reactive and on irradiation in acetone yields the cyclized products (317). The reaction involves hydrogen abstraction to yield the biradical (318) which subsequently bonds to afford the observed products. A recent study has examined the behaviour of the anion (319) in an attempt to reduce electron transfer processes. In t-butanol irradiation affords the solvent addition product (320) as the principal product presumably by a free radical path. Minor products (321) and (322) are also formed but are probably artefacts of the work-up procedure. Irradiation of (319) in methanol with added cyclohexene follows a different reaction path. In this system the reaction with methanol is minor while the dominant reaction is addition of the alkene to afford the adduct (323) in 20 % yield. The Dewar benzene derivative (324) is photocheraically unstable and irradiation affords t etramet hyl cyclobutadiene. ... [Pg.229]

Polymerization reactions require stringent operating conditions for continuous production of quality resins. In this paper the chain-growth polymerization of styrene initiated with n-butyllithium in the presence of a solvent is described. A perfectly mixed isothermal, constant volume reactor is employed. Coupled kinetic relationships descriptive of the initiator, monomer, polystyryl anion and polymer mass concentration are simulated. Trommsdorff effects (1) are incorporated. Controlled variables include number average molecular weight and production rate of total polymer. Manipulated variables are flow rate, input monomer concentration, and input initiator concentration. The... [Pg.4]


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See also in sourсe #XX -- [ Pg.179 ]




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