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Salt refining

However, in the period from 1992 to 1995, because of logistics and legal issues, the supply of potassium iodate to salt-refining companies was often disrupted. In many of the country s regions, there were accusations that the addition of iodine to salt was not being carried out in the appropriate ratio (Knobel and Medeiros-Neto, 2004 Medeiros Neto, 1998 Nimer, 1997). [Pg.1207]

Iodine nutritional risk in Brazil the socioeconomic situation and the country s size mean many people live without access to seafood. Pohtical factors affect iodine nutritional status because, the supply of potassium iodate from government to the salt-refining companies was discontinued in several Brazilian regions. [Pg.1211]

Figure 4.7 Principle of the molten salt refining process for aluminium. Figure 4.7 Principle of the molten salt refining process for aluminium.
IB. Recrystallized Salt. Section 7.1.5.3 on salt refining also mentioned the salt recrystallization process. The product is an alternative to vacuum-purified or vacuum-pan salt. To the chlor-alkali producer, the differences among all these evaporated/crystallized products come down to a value analysis of material cost vs in-plant processing cost. [Pg.635]

The principal use of AIF. is as a makeup ingredient in the molten cryoflte, Na.. AIF AI2O2, bath used in aluminum reduction cells in the HaH-Haroult process and in the electrolytic process for refining of aluminum metal in the Hoopes cell. A typical composition of the molten salt bath is 80—85%... [Pg.140]

AH corrosion inhibitors in use as of this writing are oil-soluble surfactants (qv) which consist of a hydrophobic hydrocarbon backbone and a hydrophilic functional group. Oil-soluble surfactant-type additives were first used in 1946 by the Sinclair Oil Co. (38). Most corrosion inhibitors are carboxyhc acids (qv), amines, or amine salts (39), depending on the types of water bottoms encountered in the whole distribution system. The wrong choice of inhibitors can lead to unwanted reactions. Eor instance, use of an acidic corrosion inhibitor when the water bottoms are caustic can result in the formation of insoluble salts that can plug filters in the distribution system or in customers vehicles. Because these additives form a strongly adsorbed impervious film at the metal Hquid interface, low Hquid concentrations are usually adequate. Concentrations typically range up to 5 ppm. In many situations, pipeline companies add their own corrosion inhibitors on top of that added by refiners. [Pg.186]

Aromatic Isocyanates. A variety of methods are described in the Hterature for the synthesis of aromatic isocyanates. Only the phosgenation of amines or amine salts is used on a commercial scale (5). Much process refinement has occurred to minimise the formation of disubstituted ureas arising by the reaction of the generated isocyanate with the amine starting material. A listing of the key commercially available isocyanates is presented in Table 1. [Pg.452]

Two types of magnesia, caustic-calcined and periclase (a refractory material), are derived from dolomitic lime. Lime is required in refining food-grade salt, citric acid, propjiene and ethylene oxides, and ethylene glycol, precipitated calcium carbonate, and organic salts, such as calcium stearate, lactate, caseinate. [Pg.178]

Lithium is used in metallurgical operations for degassing and impurity removal (see Metallurgy). In copper (qv) refining, lithium metal reacts with hydrogen to form lithium hydride which subsequendy reacts, along with further lithium metal, with cuprous oxide to form copper and lithium hydroxide and lithium oxide. The lithium salts are then removed from the surface of the molten copper. [Pg.224]

Interfdci l Composite Membra.nes, A method of making asymmetric membranes involving interfacial polymerization was developed in the 1960s. This technique was used to produce reverse osmosis membranes with dramatically improved salt rejections and water fluxes compared to those prepared by the Loeb-Sourirajan process (28). In the interfacial polymerization method, an aqueous solution of a reactive prepolymer, such as polyamine, is first deposited in the pores of a microporous support membrane, typically a polysulfone ultrafUtration membrane. The amine-loaded support is then immersed in a water-immiscible solvent solution containing a reactant, for example, a diacid chloride in hexane. The amine and acid chloride then react at the interface of the two solutions to form a densely cross-linked, extremely thin membrane layer. This preparation method is shown schematically in Figure 15. The first membrane made was based on polyethylenimine cross-linked with toluene-2,4-diisocyanate (28). The process was later refined at FilmTec Corporation (29,30) and at UOP (31) in the United States, and at Nitto (32) in Japan. [Pg.68]

Sla.g ReHning. Unwanted constituents can be removed by transfer into a slag phase. Slag refining is also used for operations in which the Hquid metal is maintained in contact with a slag or a molten salt. This second immiscible Hquid is usually more oxidizing than the metallic phase and selective oxidation of the impurities renders them soluble in the slag or molten salt. Impurities that are less easily oxidized remain in the Hquid metal. [Pg.169]

Electrorefining. Electrolytic refining is a purification process in which an impure metal anode is dissolved electrochemicaHy in a solution of a salt of the metal to be refined, and then recovered as a pure cathodic deposit. Electrorefining is a more efficient purification process than other chemical methods because of its selectivity. In particular, for metals such as copper, silver, gold, and lead, which exhibit Htfle irreversibHity, the operating electrode potential is close to the reversible potential, and a sharp separation can be accompHshed, both at the anode where more noble metals do not dissolve and at the cathode where more active metals do not deposit. [Pg.175]

The approximate worldwide aimual usage of nickel chemicals at 10 t, other than for steel and nickel refining, in 1994 was, for plating salts, 12—15 catalysts, 10—12 specialty ceramics, 3—4 specialty chemicals, 2—3 and other specialties, 1—2. [Pg.13]

Other Specialty Chemicals. In fuel-ceU technology, nickel oxide cathodes have been demonstrated for the conversion of synthesis gas and the generation of electricity (199) (see Fuel cells). Nickel salts have been proposed as additions to water-flood tertiary cmde-oil recovery systems (see Petroleum, ENHANCED oil recovery). The salt forms nickel sulfide, which is an oxidation catalyst for H2S, and provides corrosion protection for downweU equipment. Sulfur-containing nickel complexes have been used to limit the oxidative deterioration of solvent-refined mineral oils (200). [Pg.15]

A process has been developed (139) whereby up to 80% of the oil can be removed from whole, raw peanuts without the use of solvent. In this process, the blanched peanuts are brought to a proper moisture content, pressed mechanically, and then reshaped or reconstituted by dipping in hot water subsequently they can be roasted and salted, or used in confections or other formulations. Defatted peanuts may also be ground into meal and added to cookies, cakes, and many other products, where they impart a distinctly nutty flavor and cmnchy texture. On the other hand, the resulting high grade oil is refined and employed in cooking and industrial products. This process can also be used for pecans, walnuts, almonds, Brazil nuts, cashews, and other nuts (140-142). [Pg.278]

Crude oil is recovered from the reservoir mixed with a variety of substances gases, water, and dirt (minerals) (4). Thus, refining actually commences with the production of fluids from the weU or reservoir and is followed by pretreatment operations that are appHed to the cmde oil either at the refinery or prior to transportation. Pipeline operators, for iastance, are iasistent upon the quahty of the fluids put iato the pipelines therefore, any cmde oil to be shipped by pipeline or, for that matter, by any other form of transportation must meet rigid specifications ia regard to water and salt content. In some iastances, sulfur content, nitrogen content, and viscosity may also be specified. [Pg.201]

In this process, uranium metal is electrodeposited at the cathode, while plutonium and other transuranium elements remain in the molten salt as trichlorides. Plutonium is reduced in a second step at a metallic cathode to produce Cd—Pu intermetallics. The refined plutonium and uranium metals can then be refabricated into metallic fuel (137). [Pg.201]


See other pages where Salt refining is mentioned: [Pg.1259]    [Pg.329]    [Pg.1259]    [Pg.329]    [Pg.63]    [Pg.514]    [Pg.525]    [Pg.347]    [Pg.348]    [Pg.379]    [Pg.379]    [Pg.385]    [Pg.455]    [Pg.48]    [Pg.145]    [Pg.155]    [Pg.331]    [Pg.368]    [Pg.496]    [Pg.301]    [Pg.469]    [Pg.511]    [Pg.9]    [Pg.64]    [Pg.18]    [Pg.176]    [Pg.201]    [Pg.522]    [Pg.529]    [Pg.531]    [Pg.537]    [Pg.101]    [Pg.332]   
See also in sourсe #XX -- [ Pg.478 ]




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Molten salt refining

Refining of Salt

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