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Carbon raw materials

This route has been completely displaced, first by chlorination and dehydro-chlorination of ethylene or vinyl chloride, and more recendy by oxychlorination of two-carbon raw materials (2) (see Chlorocarbonsandchlorohydrocarbons). [Pg.102]

The term activation refers to the development of the adsorption properties of carbon. Raw materials such as coal and charcoal do have some adsorption capacity, but this is greatly enhanced by the activation process. There are three main forms of activated carbon. [Pg.404]

The carbon raw material in the form of coke, coal or natural or synthetic graphite is ground and sieved (following calcination at 700-1300°C to control volatiles, if necessary) to give a desired particle size distribution. The distribution depends upon the size of the artifact to be formed and the method of forming. [Pg.863]

CFx)n has a remarkable range of physical and chemical properties and as a result it has found several applications similar to plastics in modern industry, The product made in one plant may be different from the one made in another plant, even if both the plants follow the same procedure, due to the uniqueness and diversity of the carbon raw material, fluorine content, and fluorination conditions. There arc an infinite variety of carbon structures that can be selected for fluorination and the products can be obtained for use in vastly different applications. In short, the origin and physical structures of the carbon raw material influence fluorination... [Pg.218]

Figure 4. Generation of porosity in powdered activated carbon by steam treatment. Note For clarity, all planes are oriented in such a way that they are viewed from the edge. In reality, any orientation will be found. A. Structure of carbonized raw material showing basal planes (B) and active basal planes (AB). B. Development of microporosity after active basal planes are gasified. C. Subsequent thermal treatment generates additional active basal planes. D. Development of mesoporosity and additional microporosity after more active basal planes are gasified. B = basal plane AB= active basal plane xp = micropore Mp = mesopores. (Courtesy Norit Nederland B.V.)... Figure 4. Generation of porosity in powdered activated carbon by steam treatment. Note For clarity, all planes are oriented in such a way that they are viewed from the edge. In reality, any orientation will be found. A. Structure of carbonized raw material showing basal planes (B) and active basal planes (AB). B. Development of microporosity after active basal planes are gasified. C. Subsequent thermal treatment generates additional active basal planes. D. Development of mesoporosity and additional microporosity after more active basal planes are gasified. B = basal plane AB= active basal plane xp = micropore Mp = mesopores. (Courtesy Norit Nederland B.V.)...
BRN 2254088 Carbonic acid, cyclooctyl methyl ester Cyclooctyl methyl carbonate EINECS 262-912-7 Jasmacyclat Methyl cyclooctyl carbonate. Raw material for fragrance in floral notes. Henkel/Cospha. [Pg.355]

Physical activation converts the carbonized raw material into a product that contains an extremely high surface area and a porous structure of molecular dimensions. The aim of this process is to enhance the volume and to enlarge the diameters of the pores formed during carbonization and to create some new porosity. Physical activation is usually carried out at temperatures between 800 and 1000°C in the presence of suitable oxidizing gases such as steam, CO2 or air, or any mixture of these gases. [Pg.72]

Gasification of the carbonized raw material with steam and carbon dioxide occurs by the following endothermic reactions ... [Pg.73]

Adsorption. Adsorption involves the transfer of a component onto a solid surface. An example is the adsorption of organic vapors by activated carbon. Activated carbon is a highly porous form of carbon manufactured from a variety of carbonaceous raw materials such as coal or wood. The adsorbent may need to be... [Pg.108]

Chemists make compounds and strive to understand their reactions. My own interest lies in the chemistry of the compounds of the elements carbon and hydrogen, called hydrocarbons. These make up petroleum oil and natural gas and thus are in many ways essential for everyday life. They generate energy and heat our houses, fuel our cars and airplanes and are raw materials for most manmade materials ranging from plastics to pharmaceuticals. Many of the chemical reactions essential to hydrocarbons are catalyzed by acids and proceed through positive ion intermediates, called carbocations. [Pg.182]

Oxygen is the most abundant element on earth The earths crust is rich in carbonate and sili cate rocks the oceans are almost entirely water and oxygen constitutes almost one fifth of the air we breathe Carbon ranks only fourteenth among the elements in natural abundance but trails only hydro gen and oxygen in its abundance in the human body It IS the chemical properties of carbon that make it uniquely suitable as the raw material forthe building blocks of life Let s find out more about those chemi cal properties... [Pg.6]

Prostaglandins arise from unsaturated C20 carboxylic acids such as arachidonic acid (see Table 26 1) Mammals cannot biosynthesize arachidonic acid directly They obtain Imoleic acid (Table 26 1) from vegetable oils m their diet and extend the car bon chain of Imoleic acid from 18 to 20 carbons while introducing two more double bonds Lmoleic acid is said to be an essential fatty acid, forming part of the dietary requirement of mammals Animals fed on diets that are deficient m Imoleic acid grow poorly and suffer a number of other disorders some of which are reversed on feed mg them vegetable oils rich m Imoleic acid and other polyunsaturated fatty acids One function of these substances is to provide the raw materials for prostaglandin biosynthesis... [Pg.1080]

Fig. 1. An amplified outline scheme of the making of various wiaes, alternative products, by-products, and associated wastes (23). Ovals = raw materials, sources rectangles = wines hexagon = alternative products (decreasing wine yield) diamond = wastes. To avoid some complexities, eg, all the wine vinegar and all carbonic maceration are indicated as red. This is usual, but not necessarily tme. Similarly, malolactic fermentation is desired in some white wines. FW = finished wine and always involves clarification and stabilization, as in 8, 11, 12, 13, 14, 15, 33, 34, followed by 39, 41, 42. It may or may not include maturation (38) or botde age (40), as indicated for usual styles. Stillage and lees may be treated to recover potassium bitartrate as a by-product. Pomace may also yield red pigment, seed oil, seed tannin, and wine spidts as by-products. Sweet wines are the result of either arresting fermentation at an incomplete stage (by fortification, refrigeration, or other means of yeast inactivation) or addition of juice or concentrate. Fig. 1. An amplified outline scheme of the making of various wiaes, alternative products, by-products, and associated wastes (23). Ovals = raw materials, sources rectangles = wines hexagon = alternative products (decreasing wine yield) diamond = wastes. To avoid some complexities, eg, all the wine vinegar and all carbonic maceration are indicated as red. This is usual, but not necessarily tme. Similarly, malolactic fermentation is desired in some white wines. FW = finished wine and always involves clarification and stabilization, as in 8, 11, 12, 13, 14, 15, 33, 34, followed by 39, 41, 42. It may or may not include maturation (38) or botde age (40), as indicated for usual styles. Stillage and lees may be treated to recover potassium bitartrate as a by-product. Pomace may also yield red pigment, seed oil, seed tannin, and wine spidts as by-products. Sweet wines are the result of either arresting fermentation at an incomplete stage (by fortification, refrigeration, or other means of yeast inactivation) or addition of juice or concentrate.
Low pressure methanol carbonylation transformed the market because of lower cost raw materials, gender, lower cost operating conditions, and higher yields. Reaction temperatures are 150—200°C and the reaction is conducted at 3.3—6.6 MPa (33—65 atm). The chief efficiency loss is conversion of carbon monoxide to CO2 and H2 through a water-gas shift as shown. [Pg.67]

Activated carbons are made by first preparing a carbonaceous char with low surface area followed by controlled oxidation in air, carbon dioxide, or steam. The pore-size distributions of the resulting products are highly dependent on both the raw materials and the conditions used in their manufacture, as maybe seen in Figure 7 (42). [Pg.275]

Because the higher alcohols are made by a number of processes and from different raw materials, analytical procedures are designed to yield three kinds of information the carbon chain length distribution, or combining weight, of the alcohols present the purity of the material and the presence of minor impurities and contaminants that would interfere with subsequent use of the product. Analytical methods and characterization of alcohols have been summarized (13). [Pg.443]

Raw ] Ia.teria.ls. Most of the raw materials are oxides (PbO, Ti02, Zr02) or carbonates (BaCO, SrCO, CaCO ). The levels of certain impurities and particle size are specified by the chemical suppHer. However, particle size and degree of aggregation are more difficult to specify. Because reactivity depends on particle size and the perfection of the crystals comprising the particles, the more detailed the specification, the more expensive the material. Thus raw materials are usually selected to meet appHcation-dependent requirements. [Pg.205]

The technology of urea production is highly advanced. The raw materials requited ate ammonia and carbon dioxide. Invariably, urea plants ate located adjacent to ammonia production faciUties which conveniently furnish not only the ammonia but also the carbon dioxide, because carbon dioxide is a by-product of synthesis gas production and purification. The ammonia and carbon dioxide ate fed to a high pressure (up to 30 MPa (300 atm)) reactor at temperatures of about 200°C where ammonium carbamate [111-78-0] CH N202, urea, and water ate formed. [Pg.220]

Uses. The chemical inertness, thermal stability, low toxicity, and nonflammability of PFCs coupled with their unusual physical properties suggest many useflil applications. However, the high cost of raw materials and manufacture has limited commercial production to a few, small-volume products. Carbon tetrafluoride and hexafluoroethane are used for plasma, ion-beam, or sputter etching of semiconductor devices (17) (see loN implantation). Hexafluoroethane and octafluoropropane have some applications as dielectric gases, and perfluorocyclobutane is used in minor amounts as a dielectric fluid. Perfluoro-1,3-dimethyl cyclohexane is used as an inert, immersion coolant for electronic equipment, and perfluoro-2-methyldecatin is used for... [Pg.283]

X 10 Btu/short ton), the solar energy trapped in 17.9 x 10 t of biomass, or about 8 x 10 t of biomass carbon, would be equivalent to the world s fossil fuel consumption in 1990 of 286 x 10 J. It is estimated that 77 x 10 t of carbon, or 171 x 10 t of biomass equivalent, most of it wild and not controlled, is fixed on the earth each year. Biomass should therefore be considered as a raw material for conversion to large suppHes of renewable substitute fossil fuels. Under controlled conditions dedicated biomass crops could be grown specifically for energy appHcations. [Pg.10]


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