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Heavy reduction

The density of heavy fuels is greater than 0.920 kg/1 at 15°C. The marine diesel consumers focus close attention on the fuel density because of having to centrifuge water out of the fuel. Beyond 0.991 kg/1, the density difference between the two phases —aqueous and hydrocarbon— becomes too small for correct operation of conventional centrifuges technical improvements are possible but costly. In extreme cases of fuels being too heavy, it is possible to rely on water-fuel emulsions, which can have some advantages of better atomization in the injection nozzle and a reduction of pollutant emissions such as smoke and nitrogen oxides. [Pg.236]

The vapor pressure of a crude oil at the wellhead can reach 20 bar. If it were necessary to store and transport it under these conditions, heavy walled equipment would be required. For that, the pressure is reduced (< 1 bar) by separating the high vapor pressure components using a series of pressure reductions (from one to four flash stages) in equipment called separators , which are in fact simple vessels that allow the separation of the two liquid and vapor phases formed downstream of the pressure reduction point. The different components distribute themselves in the two phases in accordance with equilibrium relationships. [Pg.319]

Refining after year 2000 will be characterized by heavy residue conversion and the reduction in aromatics content. [Pg.411]

For 1994 standards and beyond, heavy-duty tmcks must meet standards which reflect the greatest degree of emission reduction achievable through available technology. [Pg.194]

Changes in fluid compositions include the reduction and removal of zinc from hydrauHc fluids. Zinc-free antiwear hydrauHc fluids, which may be ashless and free of phenol, were developed to meet wastewater treatment regulations for industrial sites by reducing the discharge of heavy metals and phenol into waterways. [Pg.267]

Size reduction (qv) or comminution is the first and very important step in the processing of most minerals (2,6,10,20—24). It also involves large expenditures for heavy equipment, energy, operation, and maintenance. Size reduction is necessary because the value minerals are intimately associated with gangue and need to be Hberated, and/or because most minerals processing/separation methods require the ore mass to be of certain size and/or shape. Size reduction is also required in the case of quarry products to produce material of controlled particle size (see Size measurement of particles). In some instances, hberation of valuables or impurities from the ore matrix is achieved without any apparent size reduction. Scmbbers and attritors used in the industrial minerals plants, eg, phosphate, mtile, glass sands, or clay, ate examples. [Pg.396]

Rubbers. Plasticizers have been used in mbber processing and formulations for many years (8), although phthaHc and adipic esters have found Htde use since cheaper alternatives, eg, heavy petroleum oils, coal tars, and other predominandy hydrocarbon products, are available for many types of mbber. Esters, eg, DOA, DOP, and DOS, can be used with latex mbber to produce large reductions in T. It has been noted (9) that the more polar elastomers such as nitrile mbber and chloroprene are insufficiendy compatible with hydrocarbons and requite a more specialized type of plasticizer, eg, a phthalate or adipate ester. Approximately 50% of nitrile mbber used in Western Europe is plasticized at 10—15 phr (a total of 5000—6000 t/yr), and 25% of chloroprene at ca 10 phr (ca 2000 t/yr) is plasticized. Usage in other elastomers is very low although may increase due to toxicological concerns over polynuclear aromatic compounds (9). [Pg.129]

The iodate is a poison potassium iodide, however, is used in foodstuffs. Thus the iodate must be completely removed frequently by a final reduction with carbon. After re-solution in water, further purification is carried out before recrystallization. Iron, barium, carbonate, and hydrogen sulfide are used to effect precipitation of sulfates and heavy metals. [Pg.534]

Bina Selenides. Most biaary selenides are formed by beating selenium ia the presence of the element, reduction of selenites or selenates with carbon or hydrogen, and double decomposition of heavy-metal salts ia aqueous solution or suspension with a soluble selenide salt, eg, Na2Se or (NH 2S [66455-76-3]. Atmospheric oxygen oxidizes the selenides more rapidly than the corresponding sulfides and more slowly than the teUurides. Selenides of the alkah, alkaline-earth metals, and lanthanum elements are water soluble and readily hydrolyzed. Heavy-metal selenides are iasoluble ia water. Polyselenides form when selenium reacts with alkah metals dissolved ia hquid ammonia. Metal (M) hydrogen selenides of the M HSe type are known. Some heavy-metal selenides show important and useful electric, photoelectric, photo-optical, and semiconductor properties. Ferroselenium and nickel selenide are made by sintering a mixture of selenium and metal powder. [Pg.332]

Density Difference Between Particle and Liquid. Separation cannot take place if A6 = 0. Some mineral oils have the same density as water at room temperature. If it is heated to 80°C, the reduction of the density of water is less than that of the mineral oil, resulting ia the water becoming heavier. Therefore separation is possible. Dilution of a Hquid by a solvent, eg, molasses by water or heavy oil by naphtha, results ia lower density and lower viscosity of the Hquid. Solvent stripping takes place at a later stage. [Pg.402]

Chemical Oxidation. Chemical oxidation can be appHed ia iadustrial wastewater pretreatment for reduction of toxicity, to oxidize metal complexes to enhance heavy metals removal from wastewaters, or as a posttreatment for toxicity reduction or priority pollutant removal. [Pg.192]

During the late 1960s and 1970s, the finding of health problems associated with heavy exposure to airborne asbestos fibers led to a strong reduction (or ban) in the use of asbestos fibers for thermal insulation. In most of the current applications, asbestos fibers are contained within a matrix, typically cement or organic resins. [Pg.344]

For heavy drain discharges of alkaline cells, there is no useful capacity after this point because the rate of discharge of the ZnMn204 is quite slow. But for lighter drain discharges, further reduction of the cathode is possible. The reaction mechanisms are not entirely clear, but there is some evidence for the formation of a final reaction product resembling hausmannite [1309-55-3] Mn O. ... [Pg.525]


See other pages where Heavy reduction is mentioned: [Pg.12]    [Pg.235]    [Pg.714]    [Pg.12]    [Pg.235]    [Pg.714]    [Pg.52]    [Pg.69]    [Pg.275]    [Pg.315]    [Pg.51]    [Pg.134]    [Pg.155]    [Pg.38]    [Pg.15]    [Pg.323]    [Pg.433]    [Pg.434]    [Pg.103]    [Pg.266]    [Pg.546]    [Pg.330]    [Pg.506]    [Pg.511]    [Pg.466]    [Pg.229]    [Pg.431]    [Pg.37]    [Pg.256]    [Pg.294]    [Pg.525]    [Pg.208]    [Pg.425]    [Pg.130]    [Pg.164]    [Pg.527]    [Pg.243]    [Pg.254]    [Pg.388]    [Pg.201]    [Pg.278]   
See also in sourсe #XX -- [ Pg.335 , Pg.342 ]




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Reduction of Heavy Metals

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