How To Preparation and Standardization of 0.1N KMnO4 Solution?

Preparation and Standardization of 0.1N KMnO₄ Solution

Preparation and Standardization of 0.1N KMnO4 Solution

Introduction

Potassium permanganate (KMnO4) is a strong oxidizing agent used in redox titrations. Since it is not a primary standard, its solution must be standardized using oxalic acid (H2C2O4·2H2O) or sodium oxalate (Na2C2O4).

Materials Required

  • Potassium permanganate (KMnO4)
  • Oxalic acid dihydrate (H2C2O4·2H2O)
  • Sulfuric acid (H2SO4, 1N)
  • Distilled water
  • Volumetric flask (1L)
  • Burette (50mL)
  • Pipette (25mL)
  • Conical flask (250mL)
  • Hot plate

Preparation of 0.1N KMnO4 Solution

Step 1: Calculate Required Amount

The equivalent weight of KMnO4 in acidic medium (MnO4 → Mn2+) is:

Eq. wt. = Molar mass / 5 = 158.034 / 5 = 31.6068 g/equivalent

For 1L of 0.1N solution:

Required KMnO4 = 0.1 × 31.6068 = 3.1607 g

Step 2: Solution Preparation

  1. Weigh approximately 3.2-3.3g of KMnO4 (to account for impurities)
  2. Dissolve in 1L distilled water in a volumetric flask
  3. Boil the solution for 15-30 minutes to destroy organic impurities
  4. Cool and filter through glass wool to remove MnO2
  5. Store in an amber bottle

Standardization with Oxalic Acid

Step 1: Prepare 0.1N Oxalic Acid

Equivalent weight of oxalic acid dihydrate:

Eq. wt. = 126.07 / 2 = 63.035 g/equivalent

For 250mL of 0.1N solution:

Required oxalic acid = 0.1 × 63.035 × 0.25 = 1.5759 g

Step 2: Titration Procedure

  1. Pipette 25mL of 0.1N oxalic acid into a conical flask
  2. Add 20mL of 1N H2SO4
  3. Heat the solution to 60-70°C
  4. Titrate with KMnO4 solution until a faint pink color persists for 30 seconds
  5. Repeat for concordant readings

Step 3: Calculations

The redox reaction:

2MnO4 + 5C2O42- + 16H+ → 2Mn2+ + 10CO2 + 8H2O

Normality calculation:

NKMnO4 = (NOxalic × VOxalic) / VKMnO4

Burette Reading (mL) Initial Final Used
Trial 1 0.00 24.50 24.50
Trial 2 0.00 24.40 24.40

Example calculation:

N = (0.1 × 25) / 24.5 = 0.102N

Precautions

  • Always perform titration in H2SO4 medium (HCl interferes due to Cl oxidation)
  • Maintain temperature between 60-70°C during titration
  • The first permanent pink color indicates the endpoint (excess MnO4)
  • Filter the KMnO4 solution to remove MnO2 precipitates
  • Store in amber bottles as KMnO4 is light-sensitive

Conclusion

The standardized 0.1N KMnO4 solution can now be used for various redox titrations including estimation of Fe2+, H2O2, and other reducing agents. Record the exact normality for accurate calculations in subsequent experiments.

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