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Removal of Produces

The liquid fractions after pretreatment were fermented using baker s yeast (Jastbolaget AB, Rotebro, Sweden) to determine the toxicity of the samples. Fermentation was carried out in 25-cm3 glass flasks, sealed with rubber stoppers and equipped with cannulas for removal of produced broth C02. The volume of the fermentation broth was 20 cm3 (18.5 cm3 of filtrate, 0.5 cm3 of nutrients, and 1 cm3 of inoculum). [Pg.515]

FIGURE 9.29 Roles of the membrane in membrane reactors (a) Extractor the removal of produces) increases the reaction conversion by shifting the reaction equilibrium, (b) Distributor the controlled addition of reactant(s) limits side reactions, (c) and (d) Active contactors the controlled diffusion of reactant(s) to the catalytic membrane can lead to an engineered catalytic zone. [Pg.246]

Was the waste otherwise generated by contact with the oil and gas production stream during the removal of produced water or other contaminants from the product ... [Pg.479]

The role of Co-Mo based hydrogenation catalysts is to convert organic sulfur compounds to H2S. The catalyst itself has limited ability for the removal of produced H2S, and only (1%3%) sulfur can be adsorbed by these catalysts even under equilibrium conditions. Thus, zinc oxide is used to remove H2S after hydrogenation procedure in industry. Some organic sulfur compounds can also be removed simultaneously by zinc oxide. [Pg.7]

The simplest manifestation of nonlinear kinetics is the clock reaction—a reaction exliibiting an identifiable mduction period , during which the overall reaction rate (the rate of removal of reactants or production of final products) may be practically indistinguishable from zero, followed by a comparatively sharp reaction event during which reactants are converted more or less directly to the final products. A schematic evolution of the reactant, product and intenuediate species concentrations and of the reaction rate is represented in figure A3.14.2. Two typical mechanisms may operate to produce clock behaviour. [Pg.1096]

Beryllium is added to copper to produce an alloy with greatly increased wear resistance it is used for current-carrying springs and non-sparking safety tools. It is also used as a neutron moderator and reflector in nuclear reactors. Much magnesium is used to prepare light nieial allo>s. other uses include the extraction of titanium (p. 370) and in the removal of oxygen and sulphur from steels calcium finds a similar use. [Pg.124]

Fructose (V) under similar conditions gives first the phenylhydrazonc (Va) by the direct condensation of the >C 0 group of carbon atom 2 with one molecule of phenylhydrazine. The second molecule of phenylhydrazine then oxidises the primary alcohol group of carbon atom 1 to the -CHO group by removal of two atoms of hydrogen, which as before serve to reduce the phenyl-hydrazine to aniline and ammonia. The compound (Vb) which is thus produced then undergoes direct condensation with the third molecule of phenylhydrazine, giving the osazone of fructose, or fructosazone (Vc). [Pg.137]

The modified procedure involves refluxing the N-substituted phthaUmide in alcohol with an equivalent quantity of hydrazine hydrate, followed by removal of the alcohol and heating the residue with hydrochloric acid on a steam bath the phthalyl hydtazide produced is filtered off, leaving the amine hydrochloride in solution. The Gabriel synthesis has been employed in the preparation of a wide variety of amino compounds, including aliphatic amines and amino acids it provides an unequivocal synthesis of a pure primary amine. [Pg.560]

The mixture was prepared and allowed to achieve equilibrium to it was added an excess of urea which caused the immediate precipitation as urea nitrate of the free nitric acid present. As a result of the sudden removal of the nitric acid from the mixture, the system underwent change to re-establish the equilibrium however, the use of an excess of urea removed the nitric acid as it was produced from acetyl nitrate and acetic acid, and the consumption of acetyl nitrate proceeded to completion. Thus, by following the production of urea nitrate with the time from the addition of urea, the rate of the back reaction could be determined, and by extrapolating the results to zero time the equilibrium... [Pg.80]

In 1875 Alexander M Zaitsev of the University of Kazan (Russia) set forth a gen erahzation describing the regioselectivity of p eliminations Zaitsev s rule summarizes the results of numerous experiments m which alkene mixtures were produced by p elim matron In its original form Zaitsev s rule stated that the alkene formed in greatest amount is the one that corresponds to removal of the hydrogen from the f3 carbon hav mg the fewest hydrogens... [Pg.204]

Further evidence pointing in the same direction was provided by Pierce, Wiley and Smith, who found that on steam activation of a particular char at 900°C the saturation uptake increased three-fold, yet the isotherm was still of Type I. They argued that even if the width of the pores was only two molecular diameters before activation, it would increase, by removal of oxides, during the activation so that the second Type I isotherm would correspond to pores more than two molecular diameters wide. (The alternative explanation, that activation produced new pores of the same width as the old, seems unlikely.)... [Pg.200]

Schematic diagram of an electrospray inlet/ion source. A spray produced from the high electrical voltage (HT) on the capillary moves toward a hole in the electrical counter electrode. After removal of much solvent, sample ions continue under their momentum through the hole and then through the nozzle and skimmer, where most remaining solvent is removed. Schematic diagram of an electrospray inlet/ion source. A spray produced from the high electrical voltage (HT) on the capillary moves toward a hole in the electrical counter electrode. After removal of much solvent, sample ions continue under their momentum through the hole and then through the nozzle and skimmer, where most remaining solvent is removed.
The rate of this reaction is increased by using excess ethylene glycol, and removal of the methanol is assured by the elevated temperature. Polymer is produced in the second stage after the temperature is raised above the melting point of the polymer, about 260°C. [Pg.302]

In Section 2.3.5.1 we have seen that pumping of atoms or molecules through a narrow slit, or small pinhole, whose width (or diameter) is about 20 pm at a pressure of a few torr on the high-pressure side of the aperture produces an efllisive beam. Removal of pressure... [Pg.393]

When processing municipal solid wastes, an eddy current separation unit is often used to separate aluminum and other nonferrous metals from the waste stream. This is done after removal of the ferrous metals (see Fig. 1). The eddy current separator produces an electromagnetic field through which the waste passes. The nonferrous metals produce currents having a magnetic moment that is phased to repel the moment of the appHed magnetic field. This repulsion causes the nonferrous metals to be thrown out of the process stream away from nonmetallic objects (13). [Pg.230]

Amidation. Heating of the diammonium salt or reaction of the dimethyl ester with concentrated ammonium hydroxide gives adipamide [628-94-4] mp 228°C, which is relatively insoluble in cold water. Substituted amides are readily formed when amines are used. The most industrially significant reaction of adipic acid is its reaction with diamines, specifically 1,6-hexanediamine. A water-soluble polymeric salt is formed initially upon mixing solutions of the two materials then hea ting with removal of water produces the polyamide, nylon-6,6. This reaction has been studied extensively, and the hterature contains hundreds of references to it and to polyamide product properties (31). [Pg.240]

The wastewater produced in this process consists mostly of water used in cleanup and propellant conveyance and sorting operations. Techniques such as the use of activated carbon and biological treatment are being investigated for the removal of solvents and dissolved organic compounds (143). [Pg.44]


See other pages where Removal of Produces is mentioned: [Pg.55]    [Pg.389]    [Pg.445]    [Pg.889]    [Pg.237]    [Pg.90]    [Pg.55]    [Pg.389]    [Pg.445]    [Pg.889]    [Pg.237]    [Pg.90]    [Pg.314]    [Pg.319]    [Pg.297]    [Pg.361]    [Pg.331]    [Pg.1688]    [Pg.2932]    [Pg.119]    [Pg.282]    [Pg.328]    [Pg.337]    [Pg.24]    [Pg.49]    [Pg.151]    [Pg.144]    [Pg.207]    [Pg.230]    [Pg.232]    [Pg.359]    [Pg.239]    [Pg.339]    [Pg.374]    [Pg.389]    [Pg.503]    [Pg.43]    [Pg.149]   


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