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Pollutant, partition

The values of q are plotted as a function of the equilibrium concentration. For constituents at low or moderate concentrations, the relationship between q and C can be generated. If n = 1, the (q-C) relationship will be linear (Eq. 9), and the slope of the line (i.e.,ITd) defines the adsorption distribution of the pollutant. Kd is generally identified as the distribution or partition coefficient, and is used to describe pollutant partitioning between liquid and solids only if the reactions that cause the partitioning are fast and reversible, and if the isotherm is linear. For cases where the partitioning of the pollutants can be adequately described by the distribution coefficient (i. e.,fast and reversible adsorption, with linear isotherm), the retardation factor (R) of the subsurface environment can be used as follows ... [Pg.198]

Bennett and Barter (1997) discuss the effect of partitioning-dissolution in an aqueous phase of alkylphenol. Specifically, they show that the depletion of this crude oil component affects the chemical composition of the original pollutant. Partitioning at equilibrium can be considered the maximum dissolution value of a compound under optimal solvation conditions. Partitioning-dissolution is obtained by washing the crude oil with saline water at variable temperature and pressure conditions, similar to those in the subsurface. The data reported were obtained using a partition device able to simulate the natural environmental conditions of a crude oil reservoir. The alkylphenol partition coefficients between crude oil and saline subsurface water were measured as a function of variation in pressure, temperature, and water salinity. Preliminary trials proved that the experimental device did not allow alkylphenol losses due to volatilization. [Pg.346]

Indeed, OCPs, once released into the environment, are distributed into various environmental compartments (e.g., water, soil, and biota) as a result of complex physical, chemical, and biological processes. In order to perform appropriate exposure and risk assessment analyses, multimedia models of pollutant partitioning in the environment have been developed. Properties which are at the base of such a partitioning are water solubility (WS), octanol-water partition coefficient (Ko ), soil adsorption (K ), and bioconcentration factors (BCFs) in aquatic organisms, following these four equilibriums ... [Pg.804]

S. W. Karickhoff and D. S. Brown, determination of Octanol Water Distribution Coefficients, Water Solubilities, and Sediment/Water Partitions Coefficientsfor Hydrophobic Organic Pollutants, EPA-600/4-79-032, report, EPA, Washington, D.C., 1979. [Pg.60]

Many more special-purpose software packages have been developed, particularly in teaching and research institutions. SMCM is software designed at the University of California in Los Angeles for partitioning of pollutants (19). Monte Carlo and molecular dynamic techniques have been adapted in a... [Pg.62]

Gossett RW, Brown DA, Young DR. 1983. Predicting the bioaccumulation of organic compounds in marine organisms using octanol/water partition coefficients. Mar Pollut Bull 14 387-392. [Pg.268]

The solubility of chemicals, drugs or pollutants in water (S ), in octanol (S ), their saturation concentration in air Qii), as well as their partitioning in the corresponding two-phase systems [octanol-water (P /w = Q/Cw), air-water (Pair/w = C IC ) and air-octanol (Paij/ = C /Co)] are important physicochemical parameters in medicinal chemistry and in environmental research. The following correlahons of those properties with HYBOT descriptors have been published recently [54—58] ... [Pg.143]

A number of mathematical models have been developed in recent years which attempt to predict the behavior of organic water pollutants. >2>3 Models assume that compounds will partition into various compartments in the environment such as air, water, biota, suspended solids and sediment. The input to the models includes the affinity of the compound for each of the compartments, the rate of transfer between the compartments, and the rates of various degradation processes in the various compartments. There is a growing body of data, however, which indicates that the models to date may have overlooked a small but significant interaction. A number of authors have suggested that a portion of the compounds in the aqueous phase may be bound to dissolved humic materials and are not therefore truly dissolved. [Pg.215]

Assume that between any two adjacent media (such as soli and water or water and crops) the pollutant Is partitioned In a perfectly constant manner, e.g.,... [Pg.271]

Table 6.5. Reduced partition index (IR) of trace metals in arid-zone soils incubated under saturated paste regime (after Han and Banin, 1997. Reprinted from Water Air Soil Pollut, 95, Han F.X., Banin A., Long-term transformations and redistribution of potentially toxic heavy metals in arid-zone soils. I Incubation under saturated conditions, p 411, Copyright (1997), with permission from Springer Science and Business Media)... Table 6.5. Reduced partition index (IR) of trace metals in arid-zone soils incubated under saturated paste regime (after Han and Banin, 1997. Reprinted from Water Air Soil Pollut, 95, Han F.X., Banin A., Long-term transformations and redistribution of potentially toxic heavy metals in arid-zone soils. I Incubation under saturated conditions, p 411, Copyright (1997), with permission from Springer Science and Business Media)...
Narwal R.P., Singh B.R. Effect of organic materials on partitioning, extractability and plant uptake of metals in an alum shale soil. Water Air Soil Pollut 1998 103 405M21. [Pg.346]

A great effort has also been realized to identify the physicochemical parameters that favor the elimination of numerous molecules. Partitioning of pollutants between liquid and solid phases of wastes (urban or animal), biological aerobic... [Pg.102]

Garbarini D, Lion L (1985) Evaluation of sorptive partitioning of nonionic pollutants in closed systems by headspace analysis. Environ Sci Technol 19 1122-1128... [Pg.140]

Another feature of the process is that the sorption capacity of type II organoclays is inversely related to the aqueous solubility of the NOCs (Chiou 1989). For example, the affinity of HDTMA-smectite for various phenols increases in the order phenol < chlorophenol < dichlorophenol < trichlorophenol since phenol is the most water-soluble while trichlorophe-nol is the most hydrophobic (Mortland et al. 1986, Lo et al. 1998). The relationship between the distribution (partition) coefficient in a type II organoclay and water-solubility is illustrated in Fig. 5 for a range of nonionic organic pollutants. [Pg.155]

Fig. 5. Relationship between the distribution (partition) coefficient on dimethyl dihydrogenated tallow montmorillonite for a range of non-ionic organic pollutants and their corresponding solubility in water. BHC is benzene hexachloride, the y-isomer of which is known as lindane aroclor 1232 and aroclor 1252 denote mixtures of polychlorinated biphenyls containing about 32 and 52% chlorine, respectively. After Beall (2003). Fig. 5. Relationship between the distribution (partition) coefficient on dimethyl dihydrogenated tallow montmorillonite for a range of non-ionic organic pollutants and their corresponding solubility in water. BHC is benzene hexachloride, the y-isomer of which is known as lindane aroclor 1232 and aroclor 1252 denote mixtures of polychlorinated biphenyls containing about 32 and 52% chlorine, respectively. After Beall (2003).

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See also in sourсe #XX -- [ Pg.169 ]




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