Difference between revisions of "Scaling Tendencies"

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The post-scaling tendency can go over 1.0 in special cases.  If you have disabled a solid from forming (via the Menu Item: Chemistry: Model Options: Phases Tab) then it is possible to have a scaling tendency greater than 1.0.  Also if the temperature is above a solid’s Temperature Range ('''[[TRANGE]]''') then it can also be above 1.0.  Please refer to the TRANGE support tip.
 
The post-scaling tendency can go over 1.0 in special cases.  If you have disabled a solid from forming (via the Menu Item: Chemistry: Model Options: Phases Tab) then it is possible to have a scaling tendency greater than 1.0.  Also if the temperature is above a solid’s Temperature Range ('''[[TRANGE]]''') then it can also be above 1.0.  Please refer to the TRANGE support tip.
  
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This was OLITips39.
  
 
[[Category:Tips]]
 
[[Category:Tips]]
 
[[Category:Thermodynamics]]
 
[[Category:Thermodynamics]]
 
[[Category: Scaling and solid formations]]
 
[[Category: Scaling and solid formations]]
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[[Category: Former Tips]]

Revision as of 09:41, 11 July 2016

What is a Scaling Tendency?

A scaling tendency is the ratio of the real-solution solubility product to the thermodynamic limit based on the thermodynamic equilibrium constant.

For the usage of the term in the software, it is defined as

Definition for Pre-Scaling tendencies: They are scaling tendencies of a solid before we permit any other solid phases to appear, i.e. before we allow solids to form. This measure acts as if other solids do not exist. The common ion effect is not considered while these tendencies are calculated.

Post –Scaling tendencies: Effect of common ions is considered. These tendencies are calculated after solids are formed. Technically the scaling tendencies which you see in the plot in analyzers are these post scaling tendencies.

Pre-scaling tendency is the same formula except for a situation when solids are not allowed to form. The mass transfer between LIQ phase to SOL is not considered while calculating these values. That is the only way to predict 'pre-scaling' tendencies.


For Example, Consider this dissolution

NaHCO3(s) = Na+ + HCO3-


The Ion Activity Product (IAP) is defined as the product of specific ions (in this case the ions resulting from the dissociation of a particular solid).

Let’s consider a 1.0 molal NaHCO3 solution:

IAP = gamma.Na*m.Na*gamma.HCO3*m.HCO3


Tip39 1.png


Assuming Ideal Solution Activities

gamma.Na = 1.0

gamma.HCO3 = 1.0

m.na = 1.0

m.HCO3 = 1.0


IAP = (1.0)(1.0)(1.0)(1.0) IAP = 1.0

The Solubility Product (KSP) is the thermodynamic limit of ion availability

Ksp = gamma.Na*m.Na*gamma.HCO3*m.HCO3

KSP = 0.403780


The Scaling Tendency is then the ratio of available ions to the thermodynamic limit.

ST = IAP/KSP ST = 1.0/0.403780 ST = 2.48



Was assuming ideal conditions valid??

The actual species concentration and activity coefficients are:


gamma.Na = 0.598

gamma.HCO3 = 0.596

m.na = 0.894

m.HCO3 = 0.866



This results in a different IAP

IAP= (0.598)(0.894)(0.596)(0.866)

IAP=0.276

The new Scaling Tendency is therefore:

ST = IAP/Ksp

ST = 0.276/0.40378

ST = 0.683


Why are the concentrations not equal to 1.0? Speciation and chemical equilibria tend to form complexes which provide a “Sink” for carbonate species. In this example:

CO2o = 0.016 molal

NaHCO3o = 0.101 molal

CO32- = 0.012 molal

NaCO3- = 0.004 molal


What does the Scaling Tendency Mean?

If ST < 1, then the solid is under-saturated If ST > 1, then the solid is super-saturated If ST = 1, then the solid is at saturation Scaling Index = Log (ST)

The post-scaling tendency can go over 1.0 in special cases. If you have disabled a solid from forming (via the Menu Item: Chemistry: Model Options: Phases Tab) then it is possible to have a scaling tendency greater than 1.0. Also if the temperature is above a solid’s Temperature Range (TRANGE) then it can also be above 1.0. Please refer to the TRANGE support tip.


This was OLITips39.