Chemical hazards: electrolytes, acid and gases

Inside every battery is a chemical system, and when a battery is damaged, overcharged, overheated or simply ageing, its chemicals can reach the people around it. Lead-acid batteries contain sulphuric acid and produce hydrogen. Lithium-ion batteries contain a flammable organic electrolyte with a fluorine-containing salt, and when they fail they release a mixture of flammable and toxic gases. Nickel-cadmium batteries contain a caustic alkaline electrolyte and toxic cadmium. This lesson covers those chemical hazards, how workers can be exposed, the exposure limits that apply and the first response to spills and contact.

HSE-102 covers hazard communication, and HSE-312 covers chemical handling and storage, including corrosives and eyewash stations in depth. This lesson applies those courses to batteries; hydrogen and ventilation in lead-acid rooms are covered separately in Lesson 5, and the gases from lithium-ion thermal runaway are revisited in Lessons 7 and 8.

Lead-acid electrolyte

The electrolyte in a lead-acid battery is a solution of sulphuric acid in water, typically around 30 to 40 percent acid by mass when fully charged, with a specific gravity of about 1.215 to 1.300 depending on the design. It is a corrosive liquid that causes severe burns to skin and eyes, and it can cause permanent eye damage within seconds. It also attacks clothing, metal and concrete. During charging, and especially when a cell is overcharged, fine acid mist can be carried out of vented cells with the gas, which irritates the eyes, nose, throat and lungs.

In flooded batteries the electrolyte is free liquid, so a cracked jar, a dropped cell, overfilling during watering or a tipped container of spare electrolyte can release litres of acid. VRLA batteries hold the electrolyte in an absorbent glass mat or gel, so free liquid is much less likely, but a damaged or severely overheated VRLA block can still leak acid, and the case may swell or crack. In both types, white or blue crystalline deposits around terminals and posts are corrosion products that may contain acid residues and lead compounds; they should be cleaned only with the right PPE and neutralizing agent.

Lead itself is a toxic metal. Normal battery maintenance involves little lead exposure, but cutting, grinding or handling corroded terminals, and recycling or breaking batteries, can release lead dust. Workers must not eat, drink or smoke in battery rooms and should wash their hands after battery work.

Lithium-ion electrolyte

The electrolyte in a lithium-ion cell is a lithium salt, most commonly lithium hexafluorophosphate (LiPF6), dissolved in a mixture of organic carbonate solvents such as ethylene carbonate, dimethyl carbonate and ethyl methyl carbonate. The quantity in each cell is small, typically a few grams to tens of grams, and it is sealed inside the cell, so routine work involves no exposure. The hazards arise when cells are damaged, vent or burn.

The carbonate solvents are flammable, with low flash points for some components, and their vapour forms ignitable mixtures with air. LiPF6 decomposes when exposed to moisture or heat, producing hydrogen fluoride (HF) and other fluorine compounds such as phosphoryl fluoride. HF is extremely toxic and corrosive; it penetrates the skin and binds calcium in the body, causing deep tissue damage and, in serious exposures, dangerous disturbances of heart rhythm. Even a small leak from a damaged cell can produce a sweet, solvent-like smell and irritating vapour, and it should be treated as a warning sign of a possible failure.

Nickel-cadmium electrolyte

Nickel-cadmium batteries use a potassium hydroxide electrolyte, a strong alkali that causes severe burns, especially to the eyes, where alkalis can penetrate faster and do more lasting damage than acids. Cadmium is a toxic metal and a human carcinogen. Ni-Cd batteries are less common in data centres today, mainly found in older switchgear control and some generator starting systems, but where they exist they need their own spill kits and procedures, because the neutralizing agent for an alkali is different from the one for acid.

Gases from battery failures

Lead-acid batteries produce mainly hydrogen and oxygen by electrolysis of water during charging, together with traces of other gases. When a lead-acid battery fails by overheating and dries out, hydrogen sulphide and sulphur dioxide can also be produced, recognizable by a rotten-egg or sharp smell. Lesson 5 covers hydrogen in detail.

Lithium-ion batteries in thermal runaway release a large volume of gas in a short time. Published test data, such as gas analyses from UL 9540A cell tests and research by test laboratories and universities, show that the vent gas typically contains hydrogen, carbon monoxide, carbon dioxide, methane, ethylene and other hydrocarbons, together with vaporized electrolyte solvents and smaller amounts of hydrogen fluoride and other toxic compounds. The proportions vary with chemistry, state of charge and test conditions. Many published analyses report hydrogen and carbon dioxide as major components and carbon monoxide at substantial concentrations, which means the gas is both flammable and toxic.

The vent gas is often released before any flame appears. In a closed room or cabinet it can accumulate to a flammable concentration and then ignite, causing a deflagration. This is what happened at the McMicken battery energy storage site in Arizona in 2019, discussed in Lesson 12. The same gas is also a toxic atmosphere: carbon monoxide at a few thousand parts per million can incapacitate within minutes, and HF is dangerous at a few parts per million.

Exposure limits

Occupational exposure limits in Canada are set by provincial, territorial and federal regulations, most of which adopt or are based on the threshold limit values (TLVs) published by the American Conference of Governmental Industrial Hygienists, with some provincial variations. Limits change over time, so check the current regulation for your jurisdiction. The values below are indicative and are given to show the scale of the hazard.

The scale is what matters. A single large lithium-ion cell can release tens to hundreds of litres of gas in thermal runaway; a module or rack can release many cubic metres. Even if the gas never ignites, the carbon monoxide alone can make a small room immediately dangerous. The program below estimates the CO concentration in a closed battery room after an off-gas event, using illustrative values.

# Illustrative estimate of carbon monoxide in a closed room after cell venting.
# Assumes uniform mixing and no ventilation (a simplification). Values are illustrative.
room_m3 = 6.0 * 8.0 * 3.5          # battery room volume, m3
gas_per_cell_l = 60.0              # vent gas per cell, L (illustrative)
co_fraction = 0.20                 # carbon monoxide fraction of vent gas (illustrative)
IDLH_PPM = 1200

for cells in (1, 5, 20, 80):
    co_m3 = cells * gas_per_cell_l / 1000 * co_fraction
    ppm = co_m3 / room_m3 * 1e6
    flag = "above IDLH" if ppm > IDLH_PPM else "below IDLH"
    print(f"{cells:3d} cells vent: CO about {ppm:7.0f} ppm ({flag})")

  1 cells vent: CO about      71 ppm (below IDLH)
  5 cells vent: CO about     357 ppm (below IDLH)
 20 cells vent: CO about    1429 ppm (above IDLH)
 80 cells vent: CO about    5714 ppm (above IDLH)

Even the venting of a handful of cells in a closed room can raise carbon monoxide well above occupational limits, and a module-level event of a few dozen cells can exceed the immediately dangerous level. Real rooms have ventilation and leakage, and the gas does not mix uniformly, so concentrations near the source can be much higher. This is why the response to a suspected lithium-ion off-gas event is to leave and let detection and ventilation work, not to investigate, as Lesson 11 explains.

Eyewash and emergency showers

Where workers can be exposed to battery electrolyte, OHS law requires facilities for quick flushing of the eyes and body. Provincial regulations set the details, and many reference or follow ANSI/ISEA Z358.1, which specifies flow rates, water temperature (tepid), activation and location, including reaching the unit within about 10 seconds and flushing for at least 15 minutes. HSE-312 Lesson 10 covers eyewash and showers in depth. In battery rooms, plumbed eyewash stations are preferred; self-contained units need regular fluid changes. Every unit must be inspected and activated weekly.

Spill response for acid

An acid spill from a flooded battery or a damaged VRLA block is controlled by containing it, neutralizing it and cleaning up the residue. Battery rooms with flooded batteries need spill containment under the racks, and every battery room needs a spill kit matched to the electrolyte. For sulphuric acid the usual neutralizing agent is sodium bicarbonate (baking soda) or a commercial acid neutralizer with a colour indicator. The reaction produces carbon dioxide, which fizzes, and water; when the fizzing stops and the indicator shows neutral, the residue can be absorbed and disposed of as hazardous waste under local rules.

The amount of neutralizer needed follows from the reaction \(\mathrm{H_2SO_4 + 2\,NaHCO_3 \to Na_2SO_4 + 2\,H_2O + 2\,CO_2}\). Each mole of sulphuric acid needs two moles of sodium bicarbonate. The program below estimates the bicarbonate needed for spills of different sizes.

# Sodium bicarbonate needed to neutralize a battery acid spill (illustrative values).
M_H2SO4 = 98.08     # g/mol
M_NAHCO3 = 84.01    # g/mol
density = 1.28      # g/mL, typical charged electrolyte (illustrative)
mass_fraction = 0.37  # acid by mass (illustrative)

for spill_l in (0.5, 2.0, 10.0):
    acid_g = spill_l * 1000 * density * mass_fraction
    mol_acid = acid_g / M_H2SO4
    bicarb_kg = 2 * mol_acid * M_NAHCO3 / 1000
    co2_l = 2 * mol_acid * 24.5          # L of CO2 at about 25 C
    print(f"{spill_l:5.1f} L spill: {acid_g/1000:5.2f} kg acid, "
          f"needs about {bicarb_kg:5.2f} kg NaHCO3, releases about {co2_l:5.0f} L CO2")

  0.5 L spill:  0.24 kg acid, needs about  0.41 kg NaHCO3, releases about   118 L CO2
  2.0 L spill:  0.95 kg acid, needs about  1.62 kg NaHCO3, releases about   473 L CO2
 10.0 L spill:  4.74 kg acid, needs about  8.11 kg NaHCO3, releases about  2366 L CO2

The numbers explain why spill kits hold several kilograms of neutralizer and why spills are neutralized gradually: a 10-litre spill releases over a thousand litres of carbon dioxide and can froth violently. Workers wear splash goggles and a face shield, chemical-resistant gloves and apron, and boots, and work from the edge of the spill inward. A spill of potassium hydroxide from a Ni-Cd battery needs a different agent, such as a weak acid neutralizer (boric acid or a commercial alkali neutralizer), never sodium bicarbonate.

First aid for battery chemicals

For acid or alkali in the eyes, flush immediately with tepid water for at least 15 minutes, holding the eyelids open, and get medical help. For skin contact, remove contaminated clothing and flush with water for at least 15 minutes. For inhalation of acid mist or failure gases, move to fresh air if it is safe to do so and get medical attention.

Possible hydrogen fluoride exposure from a lithium-ion electrolyte leak or fire residue needs special attention. After flushing with water, calcium gluconate gel is commonly applied to skin exposures as directed by the SDS, the site's medical protocol or a physician, because it binds fluoride ions; it is not a substitute for medical care, and anyone with a suspected HF exposure should be assessed by a medical professional promptly. Sites with lithium-ion batteries should decide in advance, with occupational health advice, whether to stock calcium gluconate gel and train first aiders to use it. HSE-110 covers first aid awareness more generally.