PH Calculations: Brønsted-Lowry Concept of Acids and Bases

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03.10.

2018

pH calculations

MUDr. Jan Pláteník, PhD

Brønsted-Lowry concept of acids and bases


• Acid is a proton donor
• Base is a proton acceptor

HCl(aq) + H2O(l) H3O+(aq) + Cl-(aq)


Acid Base Conjugate Conjugate
acid base

H2O(l) + NH3(aq) NH4+(aq) + OH-(aq)


Acid Base Conjugate Conjugate
acid base

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Which of the following are


conjugate acid-base pairs?
A) HCl, NaOH
B) H2O, OH-
C) H2SO4, SO42-
D) H2SO3, HSO3-
E) HClO4, ClO3-
F) H3C-NH2, H3C-NH3+

Autoionization of water
Water is amphoteric as it can behave both as acid and base

2 H2O(l) H3O+(aq) + OH-(aq)

Ion-product constant for water:


Kw = [H3O+][OH-] = [H+][OH-]

In pure water at 25 ºC:


[H+] = [OH-] = 1.0 × 10-7 mol/L

Kw = (1.0 × 10-7 mol/L)×( 1.0 × 10-7 mol/L) = 1.0 × 10-14 mol2/L2


Constant!

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pH
Activity = f . c
pH= -log10(activity of H+) f is activity coefficient,
f<1,
pOH= -log10(activity of OH-) c is molar concentration
Ion-product of water (constant!):
pH + pOH = 14

E.g.:
pH=7 (neutral): [H+] = 10-7 M = 0.0000001 mol/L
pH=1 (acidic): [H+] = 10-1 M = 0.1 mol/L
pH=13 (alkaline): [H+] = 10-13 M = 0.0000000000001 mol/L

Strong acid
E.g. HCl, HNO3, H2SO4
In aqueous solution fully dissociates to H+ and A−

pH of strong acid can be calculated as


pH = −log (f × [H+])

For HCl: [H+]= [HCl]

For H2SO4: [H+]= ~ [H2SO4]


(2nd H+ does not fully dissociate, Kd= ~10-2)

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Calculating the pH of strong acid solutions


Example: Calculate the pH of 0.06 mol/L HCl.

pH = − log0.06 = 1.22

If activity coefficient is known/given:


e.g. f = 0.879, then pH = − log(0.879 ×0.06) = 1.28

Calculating the pH of strong acid solutions


Example 2: Calculate the pH of 0.02 mol/L H2SO4.

pH = − log0.02 = 1.3979 = ~ 1.4

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Calculating the pH of strong acid solutions


Example 3: Calculate the pH of 1.0 × 10-10 M HCl.

pH = − log(10-10) = 10 …. alkaline?

Water contributes more protons than HCl in this case (10-7 M),
pH will be the same as in pure water, i.e. 7

Strong base
LiOH, NaOH, KOH, Ca(OH)2, Ba(OH)2
In aqueous solution fully dissociate to metal ion and OH−

pH of strong base can be calculated as


pOH = −log (f × [OH-])
pH = 14 − pOH = 14 −(−log (f × [OH-])

For NaOH: [OH-]= [NaOH]


For Ba(OH)2: [OH-]= 2 × [Ba(OH)2]

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Calculating the pH of strong base solutions


Example:
a) Calculate the pH of NaOH 0.5 mol/L.
pH = 14−(−log0.5) = ~13.7

b) If this solution is diluted 10-fold, what will be


the resulting pH?
pH = ~12.7

Weak acid
E.g. H2CO3, CH3COOH
Only some small fraction of molecules in
solution dissociates to anion and proton:
CH3COOH ↔ CH3COO− + H+
[CH3COO−] × [H+]
Kd = 
[CH3COOH]

pH = ½ × pK – ½ × log [AH]
pK = −log Kd

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• If we know pK (Kd) and concentration of a weak


acid solution, we can calculate (predict) pH of the
solution:

pH = ½ × pK – ½ × log [AH]

• If we measure pH of a weak acid solution of a


known concentration, we can determine its pK
(Kd):

pK = 2 × pH + log [AH]

Reading pK of weak acid from titration curve

Inflection point:
If weak acid is just half-titrated,
then pH = pK

[CH3COO−] . [H+]
Kd = 
[CH3COOH]

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Calculating the pH of weak acid solutions


Example: Calculate the pH of 0.01 mol/L acetic acid.
Ka = 1.8 × 10-5.

pH = ½ × pK – ½ × log [AH]

pK = −log(1.8 × 10-5) = 4.7447

pH = ½ × 4.7447 − ½ × log0.01 =
= 2.372 −(−1) = 3.372

Calculating the pH of weak acid solutions


Example 2: Calculate the pH of 0.1 mol/L hypochlorous acid.
Ka = 3.5 × 10-8.

pH = ½ × pK – ½ × log [AH]

pK = −log(3.5 × 10-8) = 7.456

pH = ½ × 7.456 − ½ × log0.1 =
= 3.728 −(−0.5) = 4.228

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Titration
• Reaction: A + B → C
• Substance A: unknown concentration,
amount (solution volume) known
• Substance B: known concentration, is used
to determine concentration of A
– added gradually to A until the reaction is just
complete, and the consumed amount is
recorded
– an indicator is needed to show that the reaction
has reached completion

Types of titration
• Neutralisation reaction (acid-base titration)

HCl + NaOH → NaCl + H2O


ionic: H+ + OH- → H2O

indicator e.g. phenolphthalein (in acid colourless, but


violet in alkali

• Precipitation reaction
• Redox reaction

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Titration calculations
Example: An unknown sample of sulfuric acid H2SO4 was titrated
with the known KOH solution. It was found that 12 mL of the
KOH c=0.1 mol/L was needed for just complete neutralisation of
10 mL H2SO4 unknown sample.
What is concentration of sulfuric acid in the sample?

Equation: H2SO4 + 2 KOH → K2SO4 + 2 H2O


Calculation: H2SO4 KOH
c1 . v1 = c2 . v2
c1 = c2 . v2/ v1
c1 = 0.1 . 12 / 10 = 0.12
Including stoichiometry : c(H2SO4) = 0.12/2 = 0.06 mol/L

Weak base
E.g. NH3(aq), organic amines
A fraction of molecules in aqueous solution
accepts proton from water:
NH3(aq) + H2O ↔ NH4+ + OH-
[NH4+] × [OH-]
Kd = 
[NH3]

pOH = ½ × pK – ½ × log [B]

pH = 14 − pOH = 14 − ½ × pK + ½ × log [B]

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Calculating the pH of weak base solutions


Example: Calculate the pH of 5 mol/L aqueous ammonia.
Kb = 1.8 × 10-5.

pH = 14 – ½ × pKb + ½ × log [B]

pKb = −log(1.8 × 10-5) = 4.745

pH = 14 − ½ × 4.7447 + ½ × log5 =
= 14 − 2.37236 + 0.349 = 11.977

Hydrolysis of salts
Reaction of dissolved salts with water, e.g.:
A) Anion from a strong acid, cation from a weak base, e.g.
NH4Cl:
NH4+ + H2O ↔ NH3 + H3O+
…pH is acidic
Cl- + H2O … no reaction

B) Anion from a weak acid, cation from a strong base, e.g.


NaHCO3:
Na+ + H2O … no reaction
…pH is alkaline
HCO3- + H2O ↔ H2CO3 + OH-

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pH of salt will be:


Anion is from…
strong acid weak acid
e.g. HCl e.g. H2CO3
Cation is from…

strong base NEUTRAL BASIC


e.g. NaOH e.g. NaCl e.g. NaHCO3

weak base ACIDIC ACIDIC/BASIC


e.g. NH4OH e.g. NH4Cl (depends on pK…)
e.g. NH4HCO3

Calculate the pH of 0.5 mol/L sodium hydrogen carbonate, NaHCO3.


The Ka1 of carbonic acid is 4.3 × 10-7.

pH = 14 – ½ × pKb + ½ × log [B]

pKa = −log(4.3 × 10-7) = 6.3665

pKb = 14 − 6.3665 = 7.6335

pH = 14 − ½ × 7.6335 + ½ × log0.5 =
= 14 − 3.81675 + (−0.1505) = 10.033

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Buffers
• Mixture of weak acid and its conjugate base (salt), e.g.:
– CH3COOH + CH3COONa
– NaH2PO4 + Na2HPO4
• Mixture of weak base and its conjugate acid (salt), e.g.:
– Tris + TrisHCl

Tris stands for: Tris(hydroxymethyl)aminomethane

Henderson-Hassebalch equation
[A−]
pH = pKa + log 
[AH]

pKa …negative log of dissociation constant of the weak acid


[A–] …substance concentration of the salt/conjugate base
[AH] …substance concentration of the weak acid

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Titration curve of sodium phosphate buffer


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9
pH of buffer

pH = pKa = 7.21
7

9:1 8:2 7:3 6:4 1:1 4:6 3:7 2:8 1:9

Acid : base ratio

How buffer works


E.g. phosphate buffer: NaH2PO4 + Na2HPO4

pH = pKa + log 

Addition of strong acid:


Na2HPO4 + HCl → NaH2PO4 + NaCl
Ionic: HPO42- + H+ → H2PO4-

pH = pKa + log 

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How buffer works


E.g. phosphate buffer: NaH2PO4 + Na2HPO4

pH = pKa + log 

Addition of strong base:


NaH2PO4 + NaOH → Na2HPO4 + H2O
Ionic: H2PO42- + OH- → HPO42- + H2O

pH = pKa + log 

Calculating the pH of buffer


Example 1: Calculate the pH of acetate buffer 0.1 mol/L, in
which the acid:salt ratio is 2:3.
Ka = 1.8 × 10-5.
pH = pKa + log [A-]/[AH]

pK = −log(1.8 × 10-5) = 4.7447

pH = 4.7447 + log 3/2 =


= 4.7447 + 0.17609 =
= 4.92

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Calculating the pH of buffer


Example 2: Calculate the pH of sodium phosphate buffer that
originated from mixing 150 mL of 0.1 M NaH2PO4 and 250 mL
of 0.05 M Na2HPO4. pKa = 7.21.

pH = pKa + log [A-]/[AH]

NaH2PO4: 0.1 mol/L × 0.15 = 0.015 mol

Na2HPO4: 0.05 mol/L × 0.25 = 0.0125 mol

pH = 7.21 + log 0.0125/0.015 =


= 7.21 + (-0.07918) =
= ~7.13

Calculating the pH of buffer


Example 3: 500 mL of Tris free base 0.1 M was combined
with 20 mL of 1 M HCl. What is predicted pH of the resulting
Tris/HCl buffer? Tris pKb = 5.98.

pH = pKa + log [A-]/[AH]


pKa = 14 – pKb

Tris free base: 0.05 mol


HCl: 0.02 mol
Tris + HCl → TrisHCl

pH = (14 – 5.98) + log (0.05-0.02)/0.02 =


= 8.02 + 0.176 =
= 8.196 = ~8.2

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