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Flammable salt wastes

The wastes from the synthesis of dibromosilane and phosphonium dibromide salt were hazardous wastes. Residue from KCs was treated with isopropanol before subjecting the residue to flammable hazardous waste. [Pg.62]

The catalytic vapor-phase oxidation of propylene is generally carried out in a fixed-bed multitube reactor at near atmospheric pressures and elevated temperatures (ca 350°C) molten salt is used for temperature control. Air is commonly used as the oxygen source and steam is added to suppress the formation of flammable gas mixtures. Operation can be single pass or a recycle stream may be employed. Recent interest has focused on improving process efficiency and minimizing process wastes by defining process improvements that use recycle of process gas streams and/or use of new reaction diluents (20-24). [Pg.123]

Historically, the Redox process was used to achieve the same purification as in the Purex process (97,129). The reagents were hexone (methyl isobutyl ketone) as the solvent, dichromate as an oxidant, and A1(N02)3 as the salting agent. The chief disadvantages of hexone are its flammability and its solubihty in water. However, because A1(N03)3 collects in the highly radioactive waste, thereby impeding the latter s further processing, the Redox process was abandoned in favor of the Purex process. [Pg.201]

Water has an unusually high (374°C) critical temperature owing to its polarity. At supercritical conditions water can dissolve gases such as 02 and nonpolar organic compounds as well as salts. This phenomenon is of interest for oxidation of toxic wastewater (see Waste treatments, hazardous waste). Many of the other more commonly used supercritical fluids are listed in Table 1, which is useful as an initial screening for a potential supercritical solvent. The ultimate choice for a specific application, however, is likely to depend on additional factors such as safety, flammability, phase behavior, solubility, and expense. [Pg.220]

Several additional favorable properties of CBPCs make them an even better candidate for stabilization. The waste form is a dense matrix, generally with very good mechanical properties. Also it is nonleachable, does not degrade over time, is neutral in pH, converts even flammable waste into nonflammable waste forms, performs well within acceptable levels in radiolysis tests, and can incorporate a range of inorganic waste streams (solids, sludge, liquids, and salts). [Pg.241]

Cleaning Up Spread the zinc out on a watch glass for about 20 min before wetting it and placing it in the nonhazardous solid waste container. Sometimes zinc dust from a reaction like this is pyrophoric (spontaneously flammable in air) because it is so finely divided and has such a large, clean surface area able to react with air. The aqueous filtrate should be neutralized with sodium carbonate, zinc salts removed by vacuum filtration, and the filtrate diluted with water and flushed down the drain. The zinc salts are placed in the nonhazardous solid waste container. The filtrate from the fractional crystallization should all be placed in the organic solvents container. Allow the solvent to evaporate from the sodium sulfate in the hood and then place it in the nonhazardous solid waste container. [Pg.481]

The Purex process has four significant advantages over the Redox process (1) Waste volumes can be made much lower, as the nitric acid used as salting agent can be removed by evaporation. (2) The solvent, TBP, is less volatile and less flammable than hexone. (3) TBP is more stable against attack by nitric acid. (4) Operating costs are lower. [Pg.461]

Spills of chemicals that do not pose a serious hazard, e.g., that are not flammable, nor particularly volatile, corrosive, or toxic, can be cleaned up by absorbing with spill-control pillows, paper towels, or specific chemicals that can inactivate or absorb spills of weak acids or bases, oils, aqueous salt solutions, etc. Use a dustpan and brush for cleanup. Wear gloves and eye protection. Dispose of waste with chemical wastes, rather than throwing it in the general waste. Clean area with soap and water after the waste has been removed. [Pg.330]


See other pages where Flammable salt wastes is mentioned: [Pg.240]    [Pg.240]    [Pg.217]    [Pg.239]    [Pg.139]    [Pg.182]    [Pg.201]    [Pg.618]    [Pg.2331]    [Pg.182]    [Pg.733]    [Pg.1811]    [Pg.89]    [Pg.390]    [Pg.397]    [Pg.144]    [Pg.369]    [Pg.708]    [Pg.310]   
See also in sourсe #XX -- [ Pg.240 ]




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