PH Calculations: Brønsted-Lowry Concept of Acids and Bases
PH Calculations: Brønsted-Lowry Concept of Acids and Bases
PH Calculations: Brønsted-Lowry Concept of Acids and Bases
2018
pH calculations
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Autoionization of water
Water is amphoteric as it can behave both as acid and base
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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−
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pH = − log0.06 = 1.22
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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−
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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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pH = ½ × pK – ½ × log [AH]
pK = 2 × pH + log [AH]
Inflection point:
If weak acid is just half-titrated,
then pH = pK
[CH3COO−] . [H+]
Kd =
[CH3COOH]
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pH = ½ × pK – ½ × log [AH]
pH = ½ × 4.7447 − ½ × log0.01 =
= 2.372 −(−1) = 3.372
pH = ½ × pK – ½ × log [AH]
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)
• 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?
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]
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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
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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
Henderson-Hassebalch equation
[A−]
pH = pKa + log
[AH]
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pH of buffer
pH = pKa = 7.21
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