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Sources of waste water

Possible sources of waste water are scrap storage area and site-drainage sand preparation [Pg.144]

The production-specific waste water quantity averages 0.5 m /t good castings. [Pg.144]


The process has two main sources of waste water. These are the condensate streams from the steam strippers. The principal pollutant in both wastewater streams is phenol. Phenol is of concern primarily because of its toxicity, oxygen depletion, and turbidity. In addition, phenol can cause objectionable taste and odor in fish flesh and potable water. [Pg.62]

Table 2 Concentration of chromium and nickel, determined by AAS, in samples taken from four sources of waste waters... Table 2 Concentration of chromium and nickel, determined by AAS, in samples taken from four sources of waste waters...
As in all the processes, the process condensate and all other sources of waste urea—NH —water contamination go to a waste recovery unit which includes a urea hydrolyzer. The final water discharge is then below 3—5 ppm of NH and urea. [Pg.305]

Water as coolant in a nuclear reactor is rendered radioactive by neutron irradiation of corrosion products of materials used in reactor constmction. Key nucHdes and the half-Hves in addition to cobalt-60 are nickel-63 [13981 -37-8] (100 yr), niobium-94 [14681-63-1] (2.4 x 10 yr), and nickel-59 [14336-70-0] (7.6 x lO" yr). Occasionally small leaks in fuel rods allow fission products to enter the cooling water. Cleanup of the water results in LLW. Another source of waste is the residue from appHcations of radionucHdes in medical diagnosis, treatment, research, and industry. Many of these radionucHdes are produced in nuclear reactors, especially in Canada. [Pg.228]

As mentioned several times Lewis acids are highly valuable catalysts but the most commonly used ones such as aluminium chloride and boron trifluoride are highly water sensitive and are not usually recovered at the end of a reaction, leading to a significant source of waste. In recent years there has been much research interest in lanthanide triflates (trifluoro-methanesulfonates) as water stable, recyclable Lewis acid catalysts. This unusual water stability opens up the possibility for either carrying out reactions in water or using water to extract and recover the catalyst from the reaction medium. [Pg.113]

Water with a salinity of less than 10,000 mg/L is considered to be a potential underground source of drinking water. By regulatory definition, deep-well injection of hazardous waste can occur only in very saline waters or brines. Actual salinities of waters in currently used deep-well injection zones vary greatly.70 Normally, the term brine is used to refer to the natural waters in deep-well injection zones. As noted above, however, this term is not technically correct if TDS levels are less than 35,000 mg/L. [Pg.809]

In New York state a reprocessing plant near Buffalo began to reprocess nuclear wastes in 1966. After 6 years Nuclear Fuel Services (NFS), a subsidiary of W.R. Grace s Davison Chemical Company, abandoned the facility. There were 2 million cubic feet of radioactive material left behind along with 600,000 gallons of radioactive liquid waste that was seeping into a creek that flows into Lake Erie the source of drinking water for Buffalo. The cost of cleanup was estimated to be 1 billion. [Pg.220]

Other than aerial application over swamps for mosquito abatement, disulfoton is not known to be used over water. Potential sources of release into surface water include discharge of waste water from disulfoton manufacturing, formulation, and packaging facilities (HSDB 1994). Leaching and runoff from treated fields, pesticide disposal pits, or hazardous waste sites may contaminate both groundwater and surface water with disulfoton. Entry into water can also occur from accidental spills. Small amounts of volatilized disulfoton may be removed from the atmosphere as a result of wet deposition and may enter surface water (Racke 1992). [Pg.145]

Due to the capacity of deep wells to store injected waste for a long period of time, if the correct measures are taken in design, construction and operation, deep well injection can provide an effective and environmentally safe method of concentrate management. The major environmental concern for deep well injection is the potential for contamination of nearby aquifers, which may be used as a source of drinking water. Six pathways have been defined that describe the potential migration of concentrate that can cause contamination of aquifers (Shammas et al. 2009 United States Environmental Protection Agency 2002) ... [Pg.46]

Individuals living in proximity to hazardous waste sites may also be exposed to 1,4-dichlorobenzene by contaminated groundwater. If residential wells are the primary source of drinking water, this may pose a risk to human health by consumption of contaminated water and by increased inhalation of and dermal contact with 1,4-dichlorobenzene during showering and bathing. 1,4-Dichlorobenzene has been detected... [Pg.207]

The major discharges from sulfuric acid alkylation are the spent caustics from the neutralization of hydrocarbon streams leaving the alkylation reactor. These wastewaters contain dissolved and suspended solids, sulfides, oils, and other contaminants. Water drawn off from the overhead accumulators contains varying amounts of oil, sulfides, and other contaminants, but is not a major source of waste. Most refineries process the waste sulfuric acid stream from the reactor to recover clean acids, use it to neutralize other waste streams, or sell it. [Pg.246]

These are relatively clean processes because care is taken to avoid loss of product through spillage. The primary source of waste material is from the washing of railroad tank cars or tankers prior to loading finished products. These wash waters are high in emulsified oil. [Pg.253]

Fig. 10. Zonation of the Larderello geothermal field derived from (a) gas analyses, and (b) stable isotope values of steam produced before and after re-injection. Distribution and characterization of geothermal subunits obtained by gas analyses have been established from a data set collected before 1989, that is, 6 years after the beginning of re-injection of waste waters. White zones represent areas that produce gas mixtures with almost the same composition as that of the original gases emerging at the surface before the exploitation of the field (Scandiffio et al. 1995). Dashed zones produce steam affected by addition of cold water (i.e., re-injected) to the geothermal system. The zonation from the isotopes was derived from an extensive survey performed in 1992. In Fig. 10b, different sources of cold water are discriminated. Abbreviations LRD = Larderello, CN = Castelnuovo, MR = Monterotondo, SS = Sasso Pisano, LGR = Lagoni Rossi, SR = Serrazzano geothermal subunits. Fig. 10. Zonation of the Larderello geothermal field derived from (a) gas analyses, and (b) stable isotope values of steam produced before and after re-injection. Distribution and characterization of geothermal subunits obtained by gas analyses have been established from a data set collected before 1989, that is, 6 years after the beginning of re-injection of waste waters. White zones represent areas that produce gas mixtures with almost the same composition as that of the original gases emerging at the surface before the exploitation of the field (Scandiffio et al. 1995). Dashed zones produce steam affected by addition of cold water (i.e., re-injected) to the geothermal system. The zonation from the isotopes was derived from an extensive survey performed in 1992. In Fig. 10b, different sources of cold water are discriminated. Abbreviations LRD = Larderello, CN = Castelnuovo, MR = Monterotondo, SS = Sasso Pisano, LGR = Lagoni Rossi, SR = Serrazzano geothermal subunits.
Prohibits discharge of any liquid hazardous waste into a surface impoundment located within 1/2 mile of a potential source of drinking water. Contains important exemption provisions. [Pg.153]


See other pages where Sources of waste water is mentioned: [Pg.633]    [Pg.144]    [Pg.633]    [Pg.144]    [Pg.77]    [Pg.291]    [Pg.153]    [Pg.2171]    [Pg.6]    [Pg.180]    [Pg.38]    [Pg.409]    [Pg.507]    [Pg.270]    [Pg.271]    [Pg.222]    [Pg.779]    [Pg.430]    [Pg.782]    [Pg.789]    [Pg.811]    [Pg.643]    [Pg.267]    [Pg.452]    [Pg.235]    [Pg.206]    [Pg.296]    [Pg.51]    [Pg.970]    [Pg.164]    [Pg.77]    [Pg.61]    [Pg.580]    [Pg.728]    [Pg.732]   


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Waste sources

Waste water

Water waste sources

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