Home / Laboratory & analysis

Titration calculator

Choose the method, enter titrant, sample and the volumes used in each replicate to get the mean content with standard deviation and confidence interval, and see whether the volume fell in the good range of the burette.

Pre-sizing and estimating tool: results do not replace design, calculations or reports signed by a licensed professional, nor verification against the applicable codes and standards.

Check
Determination

Titrant
Sample
Titration
See what was read
—Mean sample content
—

Result of each replicate

Content from each titration, with the mean and the 95% confidence interval of the mean.

Tap the chart to see the values.

Burette relative error versus volume used

Class A tolerance divided by volume, with the recommended 20% to 90% of capacity and the replicate volumes.

Tap the chart to see the values.

Next step

Take this page’s results to another calculator with the fields already filled in.

The calculation report gathers this page's inputs, results, equations, assumptions and references, with fields for project, engineer and revision. The full report also includes the charts and interpretations, in color. In the print dialog, choose Save as PDF.

Method, assumptions and references

Equations used

Analyte mass (mg) = (V − V_blank) · C · f · r · M · (V_flask ÷ V_aliquot) (V in mL, C in mol/L, r = moles of analyte per mole of titrant)
Sample by volume: mg/L = 1000 · m ÷ V_sample; % w/v = m ÷ (10 · V_sample). By mass: mg/kg = 1000 · m ÷ m_sample; % w/w = m ÷ (10 · m_sample)
Replicates: mean x̄, SD s, CV = s ÷ x̄; 95% CI = x̄ ± t(0.975; n − 1) · s ÷ √n; Grubbs G = max|xᵢ − x̄| ÷ s (ISO 5725-2)
Burette relative error = Class A tolerance ÷ (V − V_blank); recommended range: 20% to 90% of capacity

Assumptions and limits

  • Stoichiometry holds for the reaction shown; interferences, wrong pH or an unsuitable indicator change the result and are not detected by the arithmetic.
  • The confidence interval covers only scatter between replicates. Full uncertainty (factor, mass, pipet, endpoint) follows the EURACHEM/CITAC guide on measurement uncertainty.
  • Class A burette tolerances from ISO 385 and ASTM E287; the 20% to 90% criterion is practical. Grubbs critical values at 5% from ISO 5725-2 for 3 to 12 replicates.

Standards and technical documents

  • ISO 6058:1984: Water quality — Determination of calcium content — EDTA titrimetric method
  • ISO 6059:1984: Water quality — Determination of the sum of calcium and magnesium — EDTA titrimetric method
  • ISO 9297:1989: Water quality — Determination of chloride — Silver nitrate titration with chromate indicator (Mohr’s method)
  • ISO 9963-1:1994: Water quality — Determination of alkalinity — Part 1: Total and composite alkalinity
  • ISO 5813:1983: Water quality — Determination of dissolved oxygen — Iodometric method
  • APHA, AWWA, WEF. Standard Methods, 23rd ed., 2017: 2320 B, 2340 C, 3500-Ca B, 4500-Cl⁻ B, 4500-O C
  • ISO 385:2005: Laboratory glassware — Burettes; ASTM E287: Standard Specification for Laboratory Glass Graduated Burets
  • ISO 5725-2:2019: Accuracy (trueness and precision) of measurement methods and results — Part 2
  • Mendham, J. et al. Vogel’s Textbook of Quantitative Chemical Analysis, 6th ed., Prentice Hall, 2000

U.S. regulations

  • EPA 40 CFR Part 136: approved test procedures (titrimetric methods for hardness, chloride and alkalinity)
  • EPA 40 CFR Part 143: secondary drinking water standards (chloride 250 mg/L)
  • OSHA 29 CFR 1910.1450: Occupational exposure to hazardous chemicals in laboratories

Frequently asked questions

How is content calculated from a titration?

The volume used, less the blank, times the actual titrant concentration gives moles of titrant; stoichiometry converts that to moles of analyte and molar mass to mass. Dividing by the sample amount gives the content. In the example, 12.41 mL of 0.01 M EDTA with a 0.9985 factor on 50 mL of water gives about 248 mg/L of calcium hardness as CaCO₃.

What is the stoichiometry of each titration type?

Acid-base and EDTA with metals are usually 1:1. In the Mohr method each Ag⁺ precipitates one Cl⁻. In redox it depends on electrons: 1 MnO₄⁻ oxidizes 5 Fe²⁺ and 1 Cr₂O₇²⁻ oxidizes 6 Fe²⁺. In iodometry 2 S₂O₃²⁻ react with 1 I₂, so available chlorine uses 0.5 and dissolved oxygen 0.25 mol per mol of thiosulfate.

How much of the burette should I use?

Between 20% and 90% of capacity, preferably more than half. A Class A 25 mL burette may be off by 0.03 mL: with 12.4 mL used that is 0.24% of the result; with 3 mL, 1%. Above 90% the titrant may run out before the endpoint. Adjust the sample size to land in the range.

What is the blank titration for?

It subtracts titrant used by the indicator, by impurities in water and reagents and by endpoint detection. In the Mohr chloride titration the blank is often 0.2 to 0.3 mL; ignoring it overstates chloride. Run the blank with the same water and reagents as the sample.

How many replicates, and how do I spot a bad one?

At least three. The mean cuts random error, the coefficient of variation shows repeatability and the Grubbs test flags outliers: with 4 replicates, G above 1.481 is suspect at 5%. In the example the CV is 0.35% and no replicate is an outlier. Find the cause before discarding a result.

What is the difference between total and calcium hardness?

Total hardness adds calcium and magnesium and is titrated with EDTA at pH 10 with Eriochrome Black T. Calcium hardness is titrated at pH 12 to 13, where magnesium precipitates, with murexide or calcon. The difference is magnesium hardness. For the Langelier index, use calcium hardness.

Which errors hurt the result most?

Titrant not recently standardized, pH outside the method range, overshooting the endpoint, bubbles in the burette tip, reading off eye level and a dirty sample pipet. These errors are systematic and do not show up in replicate scatter. For results with legal or contract weight, use a lab accredited to ISO/IEC 17025 or certified under EPA rules.