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Waste rates

The hazardous waste flow rate into a treatment device is lOOlb/h. Calculate the waste rate leaving the unit to achieve a collection efficiency of... [Pg.445]

Total capacity = Hazardous waste rate + Nonhazardous waste rate = (11.2 Ib/day + 4000 lb/day)( day/24 h)... [Pg.535]

The design of an activated sludge system requires the determination of the following items aeration tank volume V, oxygen requirement, daily sludge wasting rate, and sludge recycle rate R. [Pg.19]

Figure 13. Single-stage aerobic waste treatment system. So = influent BOD, Sg = effluent BOD, Xr recycle biomass concentration (VVS), rF = recycle flow rate, wF = wasting rate. Figure 13. Single-stage aerobic waste treatment system. So = influent BOD, Sg = effluent BOD, Xr recycle biomass concentration (VVS), rF = recycle flow rate, wF = wasting rate.
The rate at which the catalyst is lost or degrades has a major influence on the design. If degradation is rapid, the catalyst needs to be regenerated or replaced on a continuous basis. In addition to the cost implications, there are also environmental implications, since the lost or degraded catalyst represents waste. While it is often possible to recover useful materials from degraded catalyst and to recycle those materials in the manufacture of new catalyst, this still inevitably creates waste, since the recovery of material can never be complete. [Pg.49]

Flares. Flares are used for the combustion of waste hydrocarbon gases in which the rates may vary over a wide range and for emergency releases. Steam injection is usually used to enhance mixing and the formation of a clean flame. [Pg.305]

The process is designed from a knowledge of physical concentrations, whereas aqueous effluent treatment systems are designed from a knowledge of BOD and COD. Thus we need to somehow establish the relationship between BOD, COD, and the concentration of waste streams leaving the process. Without measurements, relationships can only be established approximately. The relationship between BOD and COD is not easy to establish, since different materials will oxidize at different rates. To compound the problem, many wastes contain complex mixtures of oxidizable materials, perhaps together with chemicals that inhibit the oxidation reactions. [Pg.309]

Of the 200 million tons of municipal solid waste collected in the United States in 1993 (1), 22% was recycled while 62% was placed in landfills and 16% incinerated (2). Plastics comprised 9.3% of these materials. The number of U.S. residential collection programs increased from 1,000 in 1988 to more than 7,000 involving more than 100 million people in 1993 (2). Approximate 1994 U.S. recycling rates are given in Table 1. [Pg.229]

The thermal degradation of mixtures of the common automotive plastics polypropylene, ABS, PVC, and polyurethane can produce low molecular weight chemicals (57). Composition of the blend affected reaction rates. Sequential thermolysis and gasification of commingled plastics found in other waste streams to produce a syngas containing primarily carbon monoxide and hydrogen has been reported (58). [Pg.232]

Because of its antimicrobial activity, acrolein has found use as an agent to control the growth of microbes in process feed lines, thereby controlling the rates of plugging and corrosion (see Wastes, industrial). [Pg.128]

Combustion characteristics of consequence include the overall mechanism of soHd waste combustion, factors governing rates of waste fuels combustion, temperatures associated with waste oxidation, and pollution-formation mechanisms. [Pg.56]

Mechanisms and Rates of Combustion. AH soHd fuels and wastes bum according to a general global mechanism (Fig. 2). The soHd particle is first heated. FoHowing heating, the particle dries as the moisture bound in the pore stmcture and on the surface of the particle evaporates. Only after moisture evolution does pyrolysis initiate to any great extent. The pyrolysis process is foHowed by char oxidation, which completes the process. [Pg.56]

The rate of solid waste combustion is controlled by diffusion, rather than by reaction kinetics. In general, the time required for combustion of a single particle of waste (1) can be expressed as ... [Pg.57]

Given the mechanisms and temperatures, waste combustion systems typically employ higher percentages of excess air, and typically also have lower cross-sectional and volumetric heat release rates than those associated with fossil fuels. Representative combustion conditions are shown in Table 11 for wet wood waste with 50—60% moisture total basis, municipal soHd waste, and RDF. [Pg.58]

Vapor Pressures and Adsorption Isotherms. The key variables affecting the rate of destmction of soHd wastes are temperature, time, and gas—sohd contacting. The effect of temperature on hydrocarbon vaporization rates is readily understood in terms of its effect on Hquid and adsorbed hydrocarbon vapor pressures. For Hquids, the Clausius-Clapeyron equation yields... [Pg.47]

Mass Transfer and Kinetics in Rotary Kilns. The rates of mass transfer of gases and vapors to and from the sohds iu any thermal treatment process are critical to determining how long the waste must be treated. Oxygen must be transferred to the sohds. However, mass transfer occurs iu the context of a number of other processes as well. The complexity of the processes and the parallel nature of steps 2, 3, 4, and 5 of Figure 2, require that the parameters necessary for modeling the system be determined empirically. In this discussion the focus is on rotary kilns. [Pg.50]


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