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Solvents spent

Printing industry Heavy-metal solutions Waste ink Spent solvents Spent electroplating wastes Ink sludge containing heavy metals... [Pg.9]

Boron trifluoride catalyst may be recovered by distillation, chemical reactions, or a combination of these methods. Ammonia or amines are frequently added to the spent catalyst to form stable coordination compounds that can be separated from the reaction products. Subsequent treatment with sulfuric acid releases boron trifluoride. An organic compound may be added that forms an adduct more stable than that formed by the desired product and boron trifluoride. In another procedure, a fluoride is added to the reaction products to precipitate the boron trifluoride which is then released by heating. Selective solvents may also be employed in recovery procedures (see Catalysts,regeneration). [Pg.162]

The electrowinning process developed by Ginatta (34) has been purchased by M.A. Industries (Atlanta, Georgia), and the process is available for licensing (qv). MA Industries have also developed a process to upgrade the polypropylene chips from the battery breaking operation to pellets for use by the plastics industry. Additionally, East Penn (Lyons Station, Pennsylvania), has developed a solvent-extraction process to purify the spent acid from lead—acid batteries and use the purified acid in battery production (35). [Pg.50]

In addition, solvent extraction is appHed to the processing of other metals for the nuclear industry and to the reprocessing of spent fuels (see Nuclearreactors). It is commercially used for the cobalt—nickel separation prior to electrowinning in chloride electrolyte. Both extraction columns and mixer-settlers are in use. [Pg.172]

Nuclear Waste. NRC defines high level radioactive waste to include (/) irradiated (spent) reactor fuel (2) Hquid waste resulting from the operation of the first cycle solvent extraction system, and the concentrated wastes from subsequent extraction cycles, in a faciHty for reprocessing irradiated reactor fuel and (3) soHds into which such Hquid wastes have been converted. Approximately 23,000 metric tons of spent nuclear fuel has been stored at commercial nuclear reactors as of 1991. This amount is expected to double by the year 2001. [Pg.92]

Solvent Extraction. Solvent extraction has widespread appHcation for uranium recovery from ores. In contrast to ion exchange, which is a batch process, solvent extraction can be operated in a continuous countercurrent-fiow manner. However, solvent extraction has a large disadvantage, owing to incomplete phase separation because of solubihty and the formation of emulsions. These effects, as well as solvent losses, result in financial losses and a potential pollution problem inherent in the disposal of spent leach solutions. For leach solutions with a concentration greater than 1 g U/L, solvent extraction is preferred. For low grade solutions with <1 g U/L and carbonate leach solutions, ion exchange is preferred (23). Solvent extraction has not proven economically useful for carbonate solutions. [Pg.317]

Batch distillation (see Fig. 3) typically is used for small amounts of solvent wastes that are concentrated and consist of very volatile components that are easily separated from the nonvolatile fraction. Batch distillation is amenable to small quantities of spent solvents which allows these wastes to be recovered onsite. With batch distillation, the waste is placed in the unit and volatile components are vaporized by applying heat through a steam jacket or boiler. The vapor stream is collected overhead, cooled, and condensed. As the waste s more volatile, high vapor pressure components are driven off, the boiling point temperature of the remaining material increases. Less volatile components begin to vaporize and once their concentration in the overhead vapors becomes excessive, the batch process is terrninated. Alternatively, the process can be terrninated when the boiling point temperature reaches a certain level. The residual materials that are not vaporized are called still bottoms. [Pg.161]

Erom 1955—1975, the Ziegler-Natta catalyst (91), which is titanium trichloride used in combination with diethylaluminum chloride, was the catalyst system for propylene polymerization. However, its low activity, which is less than 1000 g polymer/g catalyst in most cases, and low selectivity (ca 90% to isotactic polymer) required polypropylene manufacturers to purify the reactor product by washing out spent catalyst residues and removing unwanted atactic polymer by solvent extraction. These operations added significantly to the cost of pre-1980 polypropylene. [Pg.203]

Recycling and Reuse 9. Recycle cooling water and treated wastewater to the extent feasible. 10. Recover and reuse spent solvents and other chemicals to the extent feasible. [Pg.59]

Chlorinated solvent vapor degreasers can be replaced with high pressure power washers which do not generate spent solvent hazardous wastes or toxic fugitive emissions. [Pg.111]

Use nonhazardous degreasers - Spent conventional degreaser solvents can be reduced or eliminated through substitution with less toxic and/or biodegradable products. [Pg.112]

SOLVENT, n.o.s. SPENT MIXED ACID see ACID MIXTURES, SPENT, NITRATING STAIN see PAINTS, ENAMELS, LACQUERS, STAINS, etc. STANNIC CHLORIDE see TIN TETRACHLORIDE 1993 ... [Pg.246]


See other pages where Solvents spent is mentioned: [Pg.347]    [Pg.348]    [Pg.209]    [Pg.347]    [Pg.348]    [Pg.209]    [Pg.331]    [Pg.403]    [Pg.647]    [Pg.359]    [Pg.284]    [Pg.80]    [Pg.52]    [Pg.476]    [Pg.499]    [Pg.522]    [Pg.202]    [Pg.202]    [Pg.552]    [Pg.3]    [Pg.81]    [Pg.227]    [Pg.161]    [Pg.406]    [Pg.11]    [Pg.505]    [Pg.500]    [Pg.500]    [Pg.500]    [Pg.2210]    [Pg.454]    [Pg.749]    [Pg.216]    [Pg.448]    [Pg.455]    [Pg.279]    [Pg.81]    [Pg.421]    [Pg.422]    [Pg.444]    [Pg.107]    [Pg.148]   
See also in sourсe #XX -- [ Pg.1555 ]

See also in sourсe #XX -- [ Pg.1555 ]

See also in sourсe #XX -- [ Pg.1555 ]




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Spent solvent wastes

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