Tidying up the environment: A journey from exponential curves to hydrodynamics in environmental batch dissolutions

This paper reviews progress made over the last decade with the shrinking object approach to the kinetics of batch dissolution. It demonstrates how the O’Connor–Greenberg equation leads to three dissolutions: those that remain well undersaturated, those that saturate with a great excess of solid left...

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Published inPure and applied chemistry Vol. 83; no. 5; pp. 1113 - 1128
Main Author Truesdale, Victor W.
Format Journal Article
LanguageEnglish
Published Berlin De Gruyter 21.02.2011
Walter de Gruyter GmbH
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Abstract This paper reviews progress made over the last decade with the shrinking object approach to the kinetics of batch dissolution. It demonstrates how the O’Connor–Greenberg equation leads to three dissolutions: those that remain well undersaturated, those that saturate with a great excess of solid left-over, and those in the middle ground where saturation is approached or attained, but where much of the solid originally added dissolves. The equations that describe these conditions are discussed, alongside sample results that validate their use with test substances, for example, salts, sucrose, silica gel, and gypsum. The equations are then shown to be consistent with the hydrodynamic approach to dissolution. Finally, further work with middle-ground dissolutions of gypsum lead to a mechanism for the back-reaction, which involves the CaSO ion-pair. After comparison with existing studies of calcium carbonate dissolution, it is argued that this is a universal mechanism for salt dissolutions. The work improves batch dissolution as a technique to the point where it can be used synergistically with chemo-stat and rotating disc approaches. Suggestions are made for greater standardization in dissolution conditions, especially in environmental work where the data collected has to have global consistency.
AbstractList This paper reviews progress made over the last decade with the shrinking object approach to the kinetics of batch dissolution. It demonstrates how the O’Connor–Greenberg equation leads to three dissolutions: those that remain well undersaturated, those that saturate with a great excess of solid left-over, and those in the middle ground where saturation is approached or attained, but where much of the solid originally added dissolves. The equations that describe these conditions are discussed, alongside sample results that validate their use with test substances, for example, salts, sucrose, silica gel, and gypsum. The equations are then shown to be consistent with the hydrodynamic approach to dissolution. Finally, further work with middle-ground dissolutions of gypsum lead to a mechanism for the back-reaction, which involves the CaSO40 ion-pair. After comparison with existing studies of calcium carbonate dissolution, it is argued that this is a universal mechanism for salt dissolutions. The work improves batch dissolution as a technique to the point where it can be used synergistically with chemo-stat and rotating disc approaches. Suggestions are made for greater standardization in dissolution conditions, especially in environmental work where the data collected has to have global consistency.
This paper reviews progress made over the last decade with the shrinking object approach to the kinetics of batch dissolution. It demonstrates how the O’Connor–Greenberg equation leads to three dissolutions: those that remain well undersaturated, those that saturate with a great excess of solid left-over, and those in the middle ground where saturation is approached or attained, but where much of the solid originally added dissolves. The equations that describe these conditions are discussed, alongside sample results that validate their use with test substances, for example, salts, sucrose, silica gel, and gypsum. The equations are then shown to be consistent with the hydrodynamic approach to dissolution. Finally, further work with middle-ground dissolutions of gypsum lead to a mechanism for the back-reaction, which involves the CaSO 4 0 ion-pair. After comparison with existing studies of calcium carbonate dissolution, it is argued that this is a universal mechanism for salt dissolutions. The work improves batch dissolution as a technique to the point where it can be used synergistically with chemo-stat and rotating disc approaches. Suggestions are made for greater standardization in dissolution conditions, especially in environmental work where the data collected has to have global consistency.
This paper reviews progress made over the last decade with the shrinking object approach to the kinetics of batch dissolution. It demonstrates how the O’Connor–Greenberg equation leads to three dissolutions: those that remain well undersaturated, those that saturate with a great excess of solid left-over, and those in the middle ground where saturation is approached or attained, but where much of the solid originally added dissolves. The equations that describe these conditions are discussed, alongside sample results that validate their use with test substances, for example, salts, sucrose, silica gel, and gypsum. The equations are then shown to be consistent with the hydrodynamic approach to dissolution. Finally, further work with middle-ground dissolutions of gypsum lead to a mechanism for the back-reaction, which involves the CaSO ion-pair. After comparison with existing studies of calcium carbonate dissolution, it is argued that this is a universal mechanism for salt dissolutions. The work improves batch dissolution as a technique to the point where it can be used synergistically with chemo-stat and rotating disc approaches. Suggestions are made for greater standardization in dissolution conditions, especially in environmental work where the data collected has to have global consistency.
Author Truesdale, Victor W.
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Snippet This paper reviews progress made over the last decade with the shrinking object approach to the kinetics of batch dissolution. It demonstrates how the...
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StartPage 1113
SubjectTerms batch dissolution
Calcium carbonate
Dissolution
dissolution hydrodynamics
dissolution kinetics
dissolution mechanism
Fluid dynamics
Fluid flow
Gypsum
Hydrodynamics
Reaction kinetics
salt dissolution
shrinking object model
Silica gel
silica gel dissolution
Silicon dioxide
Standardization
Sucrose
Title Tidying up the environment: A journey from exponential curves to hydrodynamics in environmental batch dissolutions
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