Big Chemical Encyclopedia

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

Articles Figures Tables About

Apparatus for oxidations

Liquid-phase Reactions. liquid-phase reactions in which oxidation is secured by the use of oxidizing compounds need no special apparatus in the sense that elaborate means must be provided for temperature control and heat removal. There is usually provided a kettle form of apparatus, closed to prevent the loss of volatile materials and fitted with a reflux condenser to return vaporized materials to the reaction zone, provided with suitable means for adding reactants rapidly or slowly as may be required and for removing the product and provided with adequate jackets or coils through which heating or cooling means may be circulated as required. Examples of such apparatus are scattered throughout this book, and no specific examples are required here. [Pg.549]

In the case of liquid-phase reactions in which oxidation is secured by means of atmospheric oxygen, for example, the oxidation of liquid hydro- [Pg.549]

Problem of Heat Transfer in Vapor-phase Reactions [Pg.550]

By their very nature, the vapor-phase oxidation processes result in the concentration of reaction heat in the catalyst zone, from which it must bfe removed in large quantities at high-temperature levels. Removal of heat is essential to prevent destruction of apparatus, catalyst, or raw material, and maintenance of temperature at the proper level is necessary to ensure the correct rate and degree of oxidation. With laboratory-scale apparatus, removal of this heat is relatively easy in some instances, it is even necessary to provide an external supply of heat in order to maintain the operating temperature at the proper level. With plant-scale operation and with reactions involving deep-seated oxidation, removal of heat constitutes a major problem. With limited oxidation, however, it may become necessary to supply heat even to oxidations conducted on a plant scale. [Pg.550]

Rather elaborate means have been perfected for the oxidation of the [Pg.550]


Anabolic and catabolic pathways may be segregated into different cellular compartments. In liver cells, the biosynthesis of fatty acids from acetyl-CoA occurs in the cytosol where the enzymes for both biosynthesis and the generation of NADPH are located. The degradation of fatty acids occurs within the mitochondria where the appropriate enzymes and the apparatus for oxidative phosphorylation are located (Section 9.5). Compartmentalization of metabolic pathways necessitates the provision of mechanisms by which... [Pg.117]

Silver(I) oxide [20667-12-3] M 231.7, m -200 (dec), d 7.13. Leached with hot water in a Soxhlet apparatus for several hours to remove any entrained electrolytes. [Pg.463]

Nickel reacts on heating with B, Si, P, S and the halogens, though more slowly with F2 than most metals do. It is oxidized at red heat by steam, and will dissolve in dilute mineral acids slowly in most but quite rapidly in dil HNO3. Cone HNO3, on the other hand, renders it passive and dry hydrogen halides have little effect. It has a notable resistance to attack by aqueous caustic alkalis and therefore finds used in apparatus for producing NaOH. [Pg.1149]

Krutzch, B., Goerigk, Ch., Kurze, S. et al. (1999) Process and apparatus for reducing nitrogen oxides in engine emissions, US Patent 5,921,076. [Pg.322]

Hydrothermal synthesis is a powerful method used for the fabrication of nanophase materials due to the relatively low temperature during synthesis, facile separation of nanopartides in the product, and ready availability of apparatus for such syntheses. Versatile physical and chemical properties of nanomaterials can be obtained with the use of this method that involves various techniques (e.g., control of reaction time, temperature and choice of oxidant and its concentration). Several extensive reviews are available that discuss the fundamental properties and applications of this method [2, 3]. These reviews cover the synthesis of nanomaterials with different pore textures, different types of composition [2, 4—6], and different dimensionalities in terms of morphology [6-8]. [Pg.218]

An apparatus for producing pure nitric oxide is set up as follows. As in the apparatus for preparing hydrogen chloride, a filter flask (capacity 750 c.c.) is fitted with a dropping funnel, from which 42V-sulphuric acid is dropped into concentrated sodium nitrite solution, containing 70 g. of NaN02 in 150 c.c. of water. For this amount of nitrite 250 c.c. of the 42V-acid are required. The side tube of the flask leads first to a wash-bottle with concentrated sodium (or potassium) hydroxide, and then to one with concentrated sulphuric acid. By means of a short rubber tube a T-tube is attached to the second wash-bottle. One branch of the tube is connected to a carbon dioxide Kipp, the other to the reaction vessel. The rubber tube carries a screw clip so that, at the end of the experiment, the nitric oxide generator can be removed. [Pg.357]

Patrick WH, Ir. 1966. Apparatus for controlling the oxidation-reduction potential of waterlogged soil. Nature 212 1278-1279. [Pg.273]

Fig. 7 Fluorescence spectra of a 5-PAA/PE graft (a) after treatment with 10 (filled squares), (b) after washing with THF in a Soxhlet apparatus for 24 h (open squares)-, (c) after treatment with NaOH (open circles). For comparison purposes, a fluorescence spectrum for an oxidized polyethylene Aim without any hyperbranched graft (but with - CO2H groups) that was also treated with 10 is also shown (filled circles)... Fig. 7 Fluorescence spectra of a 5-PAA/PE graft (a) after treatment with 10 (filled squares), (b) after washing with THF in a Soxhlet apparatus for 24 h (open squares)-, (c) after treatment with NaOH (open circles). For comparison purposes, a fluorescence spectrum for an oxidized polyethylene Aim without any hyperbranched graft (but with - CO2H groups) that was also treated with 10 is also shown (filled circles)...
Scheme 13. Continuous flow apparatus for the HKR of 4-hydroxy butene oxide over silica bound Co(salen) complex 37. Scheme 13. Continuous flow apparatus for the HKR of 4-hydroxy butene oxide over silica bound Co(salen) complex 37.
In atmospheric or low-pressure hydrogenation the volume of hydrogen needed for a partial or total reduction should be calculated. This is imperative for partial hydrogenations when the reduction has to be interrupted after the required volume of hydrogen has been absorbed. In exact calculations vapor pressure of the solvent used must be considered since it contributes to the total pressure in the apparatus. If oxide-type catalysts are used, the amount of hydrogen needed for the reduction of the oxides to the metals must be included in the calculation. [Pg.12]

Generally, alkoxide-derived monodisperse oxide particles have been produced by batch processes on a beaker scale. However, on an industrial scale, the batch process is not suitable. Therefore, a continuous process is required for mass production. The stirred tank reactors (46) used in industrial process usually lead to the formation of spherical, oxide powders with a broad particle size distribution, because the residence time distribution in reactor is broad. It is necessary to design a novel apparatus for a continuous production system of monodispersed, spherical oxide particles. So far, the continuous production system of monodisperse particles by the forced hydrolysis... [Pg.46]

Assemble an apparatus for preparing nitrogen(n) oxide (Fig. 86ft). Pour a concentrated solution of sulphuric acid into wash bottles 7, and fill columns 8 with phosphoric anhydride applied onto glass wool. Dissolve 15 g of potassium nitrite and 7.5 g of potassium iodide inJ75 ml of water. Pour the solution into flask 6. Pour a 50% sulphuric acid solution into dropping funnel 5. [Pg.141]

Fig. 86. Apparatus for preparing nitrogen(IV) oxide (a) and nitrogen(II) oxide (6)... Fig. 86. Apparatus for preparing nitrogen(IV) oxide (a) and nitrogen(II) oxide (6)...

See other pages where Apparatus for oxidations is mentioned: [Pg.145]    [Pg.145]    [Pg.184]    [Pg.199]    [Pg.400]    [Pg.62]    [Pg.120]    [Pg.549]    [Pg.50]    [Pg.145]    [Pg.145]    [Pg.184]    [Pg.199]    [Pg.400]    [Pg.62]    [Pg.120]    [Pg.549]    [Pg.50]    [Pg.323]    [Pg.84]    [Pg.36]    [Pg.42]    [Pg.220]    [Pg.281]    [Pg.372]    [Pg.135]    [Pg.610]    [Pg.57]    [Pg.62]    [Pg.1]    [Pg.152]    [Pg.495]    [Pg.47]    [Pg.187]    [Pg.219]    [Pg.175]    [Pg.145]    [Pg.244]    [Pg.119]    [Pg.126]    [Pg.132]    [Pg.142]   


SEARCH



Apparatus for

© 2024 chempedia.info