Gravimetric determination of sulfate as BaSO₄
Precipitate sulfate quantitatively with barium chloride, then filter, ignite and weigh the BaSO₄: the mass of a pure, stoichiometric solid reveals how much sulfate the sample contained.
Goal
Link the mass of dried BaSO₄ to the amount of sulfate via the gravimetric factor M(SO₄²⁻)/M(BaSO₄), and justify each quantitative-transfer step.
Apparatus and reagents
A sample containing sulfate, 5% barium chloride solution, dilute hydrochloric acid, beakers and a glass rod, ashless filter paper or a crucible, drying oven or muffle furnace and an analytical balance.
Procedure
- Acidify the sulfate sample slightly with dilute HCl, then add hot BaCl₂ solution slowly while stirring — the slider stands for the volume added.
- Let the precipitate digest: keeping it hot allows small BaSO₄ crystals to dissolve and redeposit on larger ones, giving particles easy to filter.
- Add a small excess of precipitant, then test the supernatant with a drop of BaCl₂ — no new clouding means precipitation is complete.
- Filter, wash until free of chloride (AgNO₃ test), ignite to constant mass and weigh; m(SO₄²⁻) = m(BaSO₄) × 96.06/233.39.
What to observe
- Fine white particles form where the BaCl₂ stream enters and slowly settle; the dense precipitate collects as a compact layer at the bottom.
- Precipitation in hot, slightly acidic solution gives larger, purer crystals than adding all the barium at once to a cold solution.
Explanation
BaSO₄ has Ksp ≈ 1.1·10⁻¹⁰, so a modest excess of Ba²⁺ drives sulfate almost completely into the solid. Because the precipitate is chemically defined and stable to ignition, its mass converts directly to sulfate through the gravimetric factor 96.06/233.39 ≈ 0.4116 — no calibration curve is needed, which makes gravimetry an absolute method.
History of the experiment
Chemists behind it
Virtual experiment: a simplified model to build intuition. It does not replace real lab work or safety training; never repeat chemistry at home without supervision.