UNDERSTANDING VARIATION IN PARTITION COEFFICIENT, Kd ...

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Humic Acids - breakdown products of cellulose from vascular plants (also see fulvic acids). Humic acids are defined as the alkaline-soluble portion of the organic material (humus) which precipitates from solution at low pH and are generally of high molecular weight (Gascoyne 1982). Hydrolysis - a chemical reaction in which a substance reacts with water to form 2 or more new substances. For example, the first hydrolysis reaction of U 4+ can be written as U 4+ + H 2O = UOH 3+ + H + . Hydrolytic Species - an aqueous species formed from a hydrolysis reaction. Ionic Potential - ratio (z/r) of the formal charge (z) to the ionic radius (r) of an ion. Isoelectric Point (iep) - pH at which a mineral’s surface has a net surface charge of zero. More precisely, it is the pH at which the particle is electrokinetically uncharged. Lignite - a coal that is intermediate in coalification between peat and subbituminous coal. Marl - an earthy substance containing 35-65% clay and 65-35% carbonate formed under marine or freshwater conditions Mass Transfer - transfer of mass between 2 or more phases that includes an aqueous solution, such as the mass change resulting from the precipitation of a mineral or adsorption of a metal on a mineral surface. Mass Transport - time-dependent movement of 1 or more solutes during fluid flow. Mire - a small piece of marshy, swampy, or boggy ground. Model Validation - integrated test of the accuracy with which a geochemical model and its thermodynamic database simulate actual chemical processes. Monomeric Species - an aqueous species containing only 1 center cation (as compared to a polymeric species). Near Field - the portion of a contaminant plume that is near the point source and whose chemical composition is significantly different from that of the uncontaminated portion of the aquifer. Peat - an unconsolidated deposit of semicarbonized plant remains in a water saturated environment. B.4
Polynuclear Species - an aqueous species containing more than 1 central cation moiety, e.g., - 4+ (UO2) 2CO3(OH) 3 and Pb4(OH) 4 . Protium (H) - stable isotope 1 H of hydrogen. Retrograde Solubility - solubility that decreases with increasing temperature, such as those of calcite (CaCO 3) and radon. The solubility of most compounds (e.g., salt, NaCl) increases with increasing temperature. Species - actual form in which a dissolved molecule or ion is present in solution. Specific Adsorption - surface complexation via a strong bond to a mineral surface. For example, several transition metals and actinides are specifically adsorbed to aluminum- and iron-oxide minerals. Sol - a homogeneous suspension or dispersion of colloidal matter in a fluid. Solid Solution - a solid material in which a minor element is substituted for a major element in a mineral structure. Thoron - name occasionally used, especially in older documents, to refer to 220 Rn which forms from the decay of thorium. Tritium (T) - radioactive isotope 3 H of hydrogen. Tritium Units - units sometimes used to report tritium concentrations. A tritium unit (TU) is equivalent to 1 atom of 3 H (tritium) per 10 18 atoms of 1 H (protium). In natural water that produces 7.2 x 10 -3 disintegrations per minute per milliliter (dpm/ml) of tritium, 1 TU is approximately equal to 3.2 picocuries/milliliter (pCi/ml). B.5
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United States Office of Air and Rad
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NOTICE The following two-volume rep
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This publication is the result of a
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TO COMMENT ON THIS GUIDE OR PROVIDE
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CONTENTS NOTICE ...................
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Concentrations Extractable Iron Con
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Appendix A - Acronyms and Abbreviat
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Figure E.1. Variation of K d for Cr
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Table 5.16. Uranium(VI) aqueous spe
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Table H.3. Simple and multiple regr
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1.0 Introduction The objective of t
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discussed. The geochemical modeling
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2.0 The K d Model The simplest and
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track many more parameters and some
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of interest. The retardation factor
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(e.g., soil). An increasing body of
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complexation constants for the cont
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the soil column. Additionally, the
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Element Table 5.2. Concentrations o
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5.2.3 Aqueous Speciation Cadmium fo
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5.2.4 Dissolution/Precipitation/Cop
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cadmium, indicating that cadmium an
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5.2.6.2.2 Limits of K d Values with
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organic chelates (e.g., EDTA). Init
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(tarapacaite) in chromium sludge fr
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K d). Soils containing Mn oxides ox
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Table 5.7. Estimated range of Kd va
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most common valence state of lead e
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Table 5.8. Lead aqueous species inc
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Under reducing conditions, galena (
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C Adsorption of lead increases with
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(Choppin, 1983). Plutonium hydrolyt
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Table 5.10. Plutonium aqueous speci
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5.6.5 Sorption/Desorption Plutonium
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content in the system. Additionally
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much greater concentrations. Thus,
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exchanged which they attributed to
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up tables was based in part on thei
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organic complexes likely predominat
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Thorium undergoes hydrolysis in aqu
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The distribution of thorium aqueous
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from about 10 -8.5 mol/l (0.0007 mg
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Based on the assumptions and limita
Page 97 and 98: 5.10 Tritium Geochemistry And K d V
Page 99 and 100: uranium. Uranium(VI) species domina
Page 101 and 102: gives 0.1 to 10 µg/l as the range
Page 103 and 104: mineral in reducing ore zones (Fron
Page 105 and 106: Percent Distribution 100 80 60 40 2
Page 107 and 108: 5.11.6 Partition Coefficient, K d ,
Page 109 and 110: No attempt was made to statisticall
Page 111 and 112: Table 5.18. Selected chemical and t
Page 113 and 114: Another objective of this report is
Page 115 and 116: 6.0 REFERENCES Adriano, D. C. 1992.
Page 117 and 118: Bensen, D. W. 1960. Review of Soil
Page 119 and 120: Metals by Geomedia. Variables, Mech
Page 121 and 122: EPA (U.S. Environmental Protection
Page 123 and 124: Griffin, R. A., A. K. Au, and R. R.
Page 125 and 126: + Keeney-Kennicutt, W. L., and J. W
Page 127 and 128: Mattigod, S. V., A. L. Page, and I.
Page 129 and 130: Oscarson, D. W., and H. B. Hume. 19
Page 131 and 132: Relyea, J. F. and D. A. Brown. 1978
Page 133 and 134: Schultz, R. K., R. Overstreet, and
Page 135 and 136: Szalay, A. 1964. “Cation Exchange
Page 137 and 138: Yariv, S., and H. Cross. 1979. Geoc
Page 139 and 140: APPENDIX A Acronyms, Abbreviations,
Page 141 and 142: PC Personal computers operating und
Page 143 and 144: A.3.0 List of Symbols and Notation
Page 145 and 146: APPENDIX B Definitions
Page 147: Clay Content - particle size fracti
Page 151 and 152: C.1.0 Background Appendix C Partiti
Page 153 and 154: Cadmium K d Table C.2. Correlation
Page 155 and 156: C.3.0 Data Set for Soils Table C.4
Page 157 and 158: Cd K d (ml/g) Clay Cont. (wt%) pH C
Page 167 and 168: D.1.0 Background Appendix D Partiti
Page 169 and 170: A second data set (see Section D.4)
Page 171 and 172: Table D.3. Correlation coefficients
Page 173 and 174: By transposing the CEC and cesium K
Page 175 and 176: Table D.6. Cesium K d values measur
Page 177 and 178: eported in Table D.8 are described
Page 179 and 180: a 1 b 1 Range of Solution Cs Concen
Page 181 and 182: Figure D.4. Generalized cesium Freu
Page 183 and 184: Table D.10. Estimated range of K d
Page 185 and 186: D.3.0 K d Data Set for Soils and Pu
Page 187 and 188: Cesium Kd (ml/g) Clay (wt.% ) Mica
Page 193 and 194: Cesium K d (ml/g) Clay (wt%) Mica (
Page 195 and 196: Bruggenwert, M. G. M., and A. Kamph
Page 197 and 198: Shiao, S. Y., P. Rafferty, R. E. Me
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E.1.0 Background Appendix E Partiti
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chromium-reductive soils may stem f
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E.2.0 Approach The approach used to
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Table E.3. Estimated range of K d v
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Table E.4. Data from Rai et al. (19
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E.4.0 References Davis, J. A. and J
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APPENDIX F Partition Coefficients F
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(CEC) of the soils. Such an anomaly
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Table F.1. Summary of K d values fo
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Figure F.2. Variation of K d as a f
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F.4.0 References Abd-Elfattah, A.,
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APPENDIX G Partition Coefficients F
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A number of investigators have exam
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pH value, which is typical of the m
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These significant reductions in ads
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This is typically accomplished by t
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The scatterplots are typically disp
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Table G.2. Regression models for pl
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G.4.0 References Barney, G. S. 1984
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Nelson, D. M., R. P. Larson, and W.
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APPENDIX H Partition Coefficients F
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1.6 ml/g for a measurement made on
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Figure H.1. Relation between stront
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Figure H.2. Relation between stront
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H.2.4 Approach Figure H.4. Relation
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A second look-up table (Table H.5)
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Sr K d (ml/g) Clay Content (%) pH C
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Sr K d (ml/g) Clay Content (%) pH C
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Sr K d (ml/g) Clay Conten t (%) pH
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Konishi, M., K. Yamamoto, T. Yanagi
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APPENDIX I Partition Coefficients F
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descriptive statistics of the thori
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Figure I.1. Linear regression betwe
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The look-up table (Table I.5) for t
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Thorium K d (ml/g) pH Clay (wt.%) C
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Rai, D., A. R. Felmy, D. A. Moore,
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J.1.0 Background Appendix J Partiti
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J.2.2 Uranium K d Studies on Soils
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Washington. The studies included an
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and then decreases with increasing
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Kd (ml/g) 100,000 10,000 1,000 100
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papers. Warnecke et al. (1984) indi
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Anderson et al. (1982) summarize an
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McKinley and Scholtis (1993) compar
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In a similar comparison of sorption
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J.3.1 K d Values as a Function ff p
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discussed, and one would have to ma
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al., 1992; and others). These refer
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· Manskaya et al. (1956) studied a
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concentrations of humic acid, there
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pH U Kd (ml/g) Clay Cont. (wt.%) CE
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J.6.0 References Ames, L. L., J. E.
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Erikson, R. L., C. J. Hostetler, R.
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R. C. Ewing. Materials Research Soc
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Sheppard, M. I., and D. H. Thibault
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Yamamoto, T., E. Yunoki, M. Yamakaw
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