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Solvay Process
Charlie

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Charlie

20. August 2026DE
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Solvay Process

How the world got cheap soda ash. Sodium carbonate is needed for glass, soap, paper and textiles, and for most of the nineteenth century it was made by the Leblanc process, which consumed sulfuric acid, belched hydrogen chloride over the countryside and left stinking heaps of calcium sulfide waste. Ernest Solvay, a Belgian gas-works chemist with no university degree, made it instead from three cheap things — salt, limestone and ammonia — in a system where the ammonia is recovered and used again. Because the ammonia circulates rather than being consumed, the real inputs are only brine and limestone, and the only bulk waste is calcium chloride. He patented it in 1861 and had a working plant at Couillet by 1863. Within forty years it had destroyed the Leblanc industry entirely.
Fortgeschritten
90 minutes

Anweisungen

1

Saturate the brine with ammonia

Work in a fume hood or outdoors. Ammonia vapour is sharp and irritating.

  1. Dissolve sodium chloride in water until no more will dissolve — a saturated brine, roughly 36 g per 100 ml at room temperature.
  2. Cool the brine in an ice bath.
  3. Add ammonia solution and keep it cold.
Order matters. Ammonia first, carbon dioxide second. Ammonia makes the solution alkaline so it can absorb far more carbon dioxide than plain brine ever would — that is the trick the whole process turns on.

Materialien für diesen Schritt:

Sodium Chloride (table salt)Sodium Chloride (table salt)40 g
Ammonia Solution (25-28%)Ammonia Solution (25-28%)50 ml
Borosilicate BeakerBorosilicate Beaker2 Stück
2

Generate and pass carbon dioxide

Carbon dioxide comes from limestone — in industry by burning it, on the bench by acid.

  1. Generate CO₂ by adding acid to calcium carbonate in a stoppered flask, or use a cylinder.
  2. Lead the gas through tubing to the bottom of the cold ammoniacal brine.
  3. Bubble steadily for 20-30 minutes, keeping the beaker in ice.

NaCl + NH₃ + CO₂ + H₂O → NaHCO₃↓ + NH₄Cl

Sodium bicarbonate is the least soluble thing in the beaker, so it is what falls out. Everything else stays dissolved. The process is a solubility trick, not an exotic reaction.

Materialien für diesen Schritt:

Calcium Carbonate (Crushed Limestone)Calcium Carbonate (Crushed Limestone)50 g
Rubber Tubing (Lab Grade)Rubber Tubing (Lab Grade)1 length
Instant-Read ThermometerInstant-Read Thermometer1 Stück
3

Filter the bicarbonate

Collect the solid and wash it.

  1. Filter the cold slurry through filter paper in a funnel.
  2. Wash the crystals with a little ice-cold water to remove ammonium chloride.
  3. Press between filter papers and let dry.
Wash with as little cold water as you can. Sodium bicarbonate is only sparingly soluble, but it is not insoluble, and a generous wash quietly dissolves your yield.

Materialien für diesen Schritt:

Filter PaperFilter Paper1 Packung
Glass Funnel (Stemmed)Glass Funnel (Stemmed)1 Stück
4

Calcine to soda ash

Heating drives the bicarbonate to the carbonate — the actual product.

  1. Heat the dried solid gently in an evaporating dish or crucible.
  2. Hold it hot until it stops losing mass.

2 NaHCO₃ → Na₂CO₃ + H₂O + CO₂↑

Weigh before and after. Theory says 168 g of bicarbonate gives 106 g of carbonate — a loss of 36.9%. Measuring close to that is your proof the reaction went as written, and the released CO₂ is recycled back to step 2 in a real plant.

Materialien für diesen Schritt:

Digital Kitchen ScaleDigital Kitchen Scale1 Stück
5

Test the product

Confirm you made carbonate and not something else.

  1. Dissolve a little in water and test with indicator — sodium carbonate is distinctly alkaline, more so than the bicarbonate you started from.
  2. Add acid: it fizzes, releasing CO₂.
Both bicarbonate and carbonate fizz with acid, so fizzing alone proves nothing. The pH difference is what separates them — that is the discriminating test.
6

History and context

Ernest Solvay was 23 and working at his uncle's gas works when he began experimenting with ammonia and brine. He was not the first to think of it — the reaction had been described in Britain decades earlier, and several attempts to industrialise it had failed. Solvay's contribution was engineering rather than chemistry: he designed a tall carbonating tower that brought gas and liquid into efficient contact, and he made the ammonia recovery work, which is what everyone before him had failed at.

Recovery is the whole economics. Ammonia is expensive; salt and limestone are nearly free. Treating the ammonium chloride with lime — itself made by burning the same limestone that supplies the CO₂ — regenerates the ammonia: 2 NH₄Cl + Ca(OH)₂ → CaCl₂ + 2 NH₃ + 2 H₂O. Run in a loop, the process consumes only brine and limestone.

Against Leblanc it was decisive: less fuel, no sulfur, no hydrogen chloride pollution, continuous rather than batch. Leblanc production in Britain collapsed over the following decades. Solvay became extremely rich and funded the Solvay Conferences, the physics meetings where quantum mechanics was argued out in the 1920s.

The honest weakness: calcium chloride. Every tonne of soda ash leaves roughly a tonne of it, and there is nothing like enough demand for it. Most is discharged, and where plants discharge to rivers or shallow seas the local salinity damage is real and well documented. A process can be a great improvement on its predecessor and still leave a serious waste problem.

Materialien

9

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