Civilization101Blueprint

Acids

Make sulphuric acid, and with it most of industrial chemistry.

Tier 3 · Medieval to early modern Materials t3-acid Blocked by prerequisites
A titration. Acids are useless until you can say how strong they are. Acid and Base Titration · 2017-06-16 · Kengksn · CC BY-SA 4.0 · Commons ↗

Everything for this step

Field guide
The sciences → 15 sections Minerals and ores → 3 sections Chemistry → 9 sections
Builds
None yet.
Reference sheets
None.
Sciences it rests on
Chemistry
Track
Chemicals, level 2 of 3 · next: Alkalis

Why this matters

Sulphuric acid is the most-produced industrial chemical in the world, and national production of it was once used as a direct proxy for industrial capacity. It gates fertiliser, explosives, dyes, batteries, metal pickling and refining. If you make one chemical, make this one.

The shape of it

  1. Get sulphur: volcanic deposits, or roast iron pyrite (fool's gold), which is common and gives sulphur dioxide directly.
  2. Bell-jar method first, at laboratory scale: burn sulphur with saltpetre in a closed glass vessel over water. The nitre supplies oxygen and the product dissolves to give dilute acid. Small, slow, and enough to learn on.
  3. Then the lead chamber process for quantity: burn sulphur and nitre in a large lead-lined chamber with steam. Lead is used because it resists the acid — this is why lead smelting matters. The process is slow and gives dilute acid, but it is entirely achievable at tier 3.
  4. Concentrate by boiling in glass or lead. Always add acid to water, never water to acid — the reverse boils violently and throws concentrated acid into your face.
  5. Then derive the others: nitric acid from saltpetre plus sulphuric acid, distilled in glass; hydrochloric acid from salt plus sulphuric acid. Between them these three make most of the rest of chemistry possible.
  6. Build the safety practice before the plant. Water supply for flushing, eye protection, ventilation, and a rule that nobody works alone. Acid burns are disfiguring and blinding, and there is no medical recovery from a serious eye exposure at this tier.
  7. Use it: superphosphate fertiliser from bone or rock phosphate (a large jump in crop yield), pickling metal before plating, battery electrolyte, and dye chemistry.

Doing it, step by step

The summary above says what has to happen. This says how, with the numbers that decide whether it works.

1 · Build the safety practice before the plant

Acid burns disfigure and blind, and there is no medical recovery from a serious eye exposure at this tier. Before any acid is made:

  • Eye protection worn by everyone in the room, always.
  • Running water within a few steps — a tank with a tap at head height — for flushing.
  • Ventilation or outdoor work: sulphur dioxide and nitrogen oxides cause serious lung injury.
  • Nobody works alone.
  • Acids stored in glass or glazed stoneware, below eye level, and away from alkalis and anything that burns.

Acid on skin or in eyes: flush with running water for at least 20 minutes. Do not neutralise on the body.

✓ Check: Eye protection, a flushing water supply and a second person are present before any acid work begins, every time.

2 · Get sulphur

Native sulphur from volcanic and some sedimentary deposits is yellow, soft, and burns with a blue flame and a choking smell. Iron pyrite — fool's gold, brassy cubes much harder than gold — is common and gives sulphur dioxide directly when roasted.

Pyrite roasting releases large volumes of sulphur dioxide: do it in a closed flue that feeds the acid process, never in open air near people. The iron oxide left behind is useful ore — see smelting.

✓ Check: The sulphur source is identified — a sample burns with a blue flame and a choking smell, or pyrite roasting gives a sharp sulphurous gas inside a flue.

3 · Learn at bell-jar scale first

Burn a little sulphur mixed with saltpetre in a dish floating on water, under a large glass bell or jar. The nitre supplies oxygen and nitrogen oxides that carry the sulphur dioxide on to sulphuric acid, which dissolves in the water below. Repeat many times with the same water to build strength.

Small, slow, and enough to learn the chemistry, the handling and the hazards before anything is scaled up. Scaling up before the small version is reliably understood is a named failure of this step.

✓ Check: Water under the bell has become acidic enough to turn red-cabbage indicator red and to dissolve a scrap of iron with bubbling.

4 · Scale up with a lead chamber

A large chamber lined with lead sheet — lead resists sulphuric acid, which is why lead smelting matters here. Sulphur dioxide from the burner, nitrogen oxides, air and steam feed in; dilute acid collects on the floor.

Chamber acid comes off at roughly 60–70%. The process is slow and continuous, and it is entirely achievable at tier 3. Keep the nitrogen oxides in the system rather than venting them — later plants recovered them in towers. Lead chambers leak where the lead is joined; inspect seams and floor regularly.

✓ Check: Acid collected from the chamber floor weighs roughly 1.5–1.6 kg per litre, and the chamber shows no leaks at its seams.

5 · Measure strength by weighing a litre, and concentrate in glass

Weigh exactly one litre at room temperature — the fastest reliable test you have:

  • Water: 1.00 kg.
  • About 62% acid: about 1.52 kg.
  • About 70%: about 1.61 kg.
  • About 98% — oil of vitriol: about 1.84 kg.

Concentrate chamber acid by boiling off water in glass or glazed stoneware, under good ventilation. Near full strength it gives off dense white fumes; stop there. Dilute acid eats iron and copper — use lead, glass or glazed stoneware.

✓ Check: Each batch has a measured weight per litre written on its label, and concentrated acid is held only in glass or glazed stoneware.

6 · Dilute acid into water — never water into acid

Mixing concentrated sulphuric acid with water releases a great deal of heat. Water poured onto acid floats, boils instantly at the surface and throws concentrated acid out of the vessel.

Pour acid slowly into a larger volume of water, in a heat-resistant vessel, stirring, in a thin stream, stopping if it gets hot. Set the vessel in a basin of cold water for large dilutions. Label the result with its strength immediately.

✓ Check: Everyone who handles acid can say, unprompted, which liquid goes into which, and has diluted a batch that way under supervision.

7 · Derive hydrochloric and nitric acid, with their hazards

  • Hydrochloric acid: heat salt with sulphuric acid; hydrogen chloride gas comes off and is absorbed in water, up to about 36%. The gas is choking and corrosive; absorb it all.
  • Nitric acid: distil saltpetre with sulphuric acid in a glass retort. It attacks almost everything except glass, gold and platinum, and stains skin yellow.

Store nitric acid away from wood, straw, oils and anything organic — it can set them alight.

Brown nitrogen dioxide fumes from nitric acid work cause delayed lung injury: the victim can feel fine and then drown in fluid in the lungs 6–24 hours later. Anyone who breathed brown fumes rests and is watched through the next day.
✓ Check: Each acid is in labelled glass with a glass stopper, nitric acid stored apart from anything organic.

8 · Use it where the return is largest: superphosphate

Phosphate is the nutrient with no substitute. Treating ground bone ash or rock phosphate with sulphuric acid converts insoluble phosphate into a form plants take up quickly — superphosphate, the first industrial fertiliser and a large jump in crop yield on phosphate-poor soil.

Mix in small batches in a lined pit under ventilation, let it cure for weeks, and dry it. Prove it on a test plot: treated and untreated strips side by side, same crop, yields weighed. Then scale. Other uses: pickling metal before plating, battery electrolyte, dye chemistry.

✓ Check: A side-by-side test plot shows a weighed yield difference between the superphosphate strip and the untreated strip.

The better path

What the record shows was done at this step, what to do instead at this tier, and the evidence. All of them: the better path.

Do not repeat

White phosphorus matches

What was done
From the 1830s, friction matches were tipped with white phosphorus, which strikes on any surface. Workers who made them absorbed it and developed 'phossy jaw' — the jawbone dying and rotting away.
Do instead
Make safety matches: keep phosphorus off the match. Red phosphorus — made by heating white phosphorus without air — goes on the striking strip, and potassium chlorate on the match head.
Evidence
Red phosphorus was identified in 1845 and the safety match patented in Sweden in 1855. White phosphorus matches were banned internationally by the Berne Convention of 1906, half a century after the safe version existed. Phossy jaw was among the grievances of the 1888 London matchgirls' strike.

Needs: Acids

How this fails

Adding water to concentrated acid.
Using iron or copper vessels, which the acid attacks.
No ventilation — sulphur dioxide and nitrogen oxides cause serious lung injury.
Scaling up before the small version is reliably understood.

How you know it worked

VerificationYou have produced concentrated sulphuric acid and used it to make superphosphate that measurably raised a crop yield.