Calculate equilibrium dissolved oxygen at 19.8 Celsius

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SUMMARY

The discussion focuses on calculating the equilibrium dissolved oxygen concentration at 19.8 degrees Celsius with a partial pressure of oxygen (PO2) at 21%. The equilibrium constant (K) was determined to be 1.475x10-3 and the calculated concentration of dissolved oxygen (O2 (aq)) is 1.256x1010 atm. The conversation also highlights the application of Henry's law and the Van 't Hoff equation to adjust Henry's coefficient for different temperatures, specifically at 7 degrees Celsius, resulting in a final concentration of 3.59x10-4 M.

PREREQUISITES
  • Understanding of Henry's law and its application in gas solubility
  • Familiarity with the Van 't Hoff equation for temperature adjustments
  • Basic knowledge of equilibrium constants and their definitions
  • Proficiency in using the ideal gas law (PV=nRT)
NEXT STEPS
  • Research the application of Henry's law in different temperature conditions
  • Study the Van 't Hoff equation and its implications for chemical equilibria
  • Explore the concept of equilibrium constants in various chemical reactions
  • Learn about the ideal gas law and its relevance in calculating gas concentrations
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Chemistry students, environmental scientists, and professionals involved in aquatic chemistry or gas solubility studies will benefit from this discussion.

spooky01
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Homework Statement


1. Calculate the equilibrium dissolved oxygen concentration for each temperature if PO2 = 21% (this means that if atmospheric pressure is 1 atm then O2 pressure is 21% of that)

Homework Equations


K19.8/RT = Kp
PV=nRT

The Attempt at a Solution


K19.8/RT = Kp

K19.8 = 1.475x10-3

(1.457x10-3)/(8.314x10-3)(273.15+19.8) = Kp

5.982x10-4 = Kp

Kp = (O2 (aq)) / (O2 (g))

5.982x10-4 = (O2 (aq)) / (0.21)

1.256x104 atm = O2 (aq)

ICE table:

__________________O2 (g)_______O2 (aq)

Initial______________0.21_________0

Change___________0.21 -x_______+x

Equilibrium_______0.21 -x_______+x5.982x10-4 = x/(0.21 – x)

5.982x10-4 (0.21 – x) = x

1.256x10-4 - 5.982x10-4 x = x

1.256x10-4 = x + 5.982x10-4 x

1.256x10-4 = 1.000598x

1.255x10-4 = x
PV = nRT

n/V = P/RT

M = 1.255x10-4 atm/(0.0821atm L/mol K) (273.15 + 19.8)

M = 5.218x10-6

This doesn't look right to me but I'm not sure what else to try. Thanks for the help!
 
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No idea what is what of what, can you please post whole question and all information given?
 
Ok I'll simplify it a bit. All I need is how to calculate the equilibrium dissolved oxygen concentration for 7 degrees celsius if PO2 = 21% (this means that if atmospheric pressure is 1 atm then O2 pressure is 21% of that). K was previously found to be 1.813x10-3 at 7 degrees celsius. My professor is asking this so there must be a way! My head hurts. The chemical equation is O2 (g) = O2 (aq), that's it.
 
What is K specifically? How is it defined?

When it comes to solubility of gases, we typically describe it with Henry's law, not with a typical equilibrium constant. These are perfectly equivalent, but you need to be sure how K is defined and what units it has.
 
K is for concentration. So if I use Henry's law, Henry's coefficient for O2 at 25 degrees celsius is 1.3×10−3 mol L/atm. How can I adjust Henry's coefficient to work at 7 degrees celsius? Thanks for the help!
 
spooky01 said:
K is for concentration.

Huh? No idea what you just said.

spooky01 said:
How can I adjust Henry's coefficient to work at 7 degrees celsius?

Van 't Hoff equation comes to mind. Yes, it requires more data. But that's a general case - every approach will require some additional information that you have not listed so far.
 
Got it. Henry's law worked!

temp 7°C

ln(kHT/kH25) = (ΔH°/R)(1/298 – 1/T)

ln(kHT/1.26x10-3mol/Latm)=(-11.71kJ/mol/8.314x10-3kJ/molK)(1/298–1/280)

ln(kHT/1.26x10-3mol/Latm) = 3.04x10-1

e ln(kHT/1.26x10-3mol/Latm) = e3.04x10-1

kHT/1.26x10-3mol/L atm = 1.36

kHT = 1.71x10-3 mol/L atmC = (1.71x10-3 mol/L atm) 0.21atm

C = 3.59x10-4 M
 

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