Sulfuric acid

Sulfuric acid (American spelling) or sulphuric acid (British spelling), also known as oil of vitriol, is a mineral acid composed of the elements sulfur, oxygen and hydrogen, with molecular formula H2SO4. It is a colourless, odourless, and viscous liquid that is soluble in water and is synthesized in reactions that are highly exothermic.[6]

"Hydrogen sulfate" and "hydrogen sulphate" redirect here. For the ion, see Sulfate § Hydrogen sulfate (bisulfate).

Sulfuric acid
Space-filling model
Ball-and-stick model length = 142.2 pm,
S-O bond length = 157.4 pm,
O-H bond length = 97 pm
Names
IUPAC name
Sulfuric acid
Other names
Oil of vitriol
Hydrogen sulfate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.028.763
EC Number
  • 231-639-5
E number E513 (acidity regulators, ...)
2122
KEGG
RTECS number
  • WS5600000
UNII
UN number 1830
Properties
H
2SO
4
Molar mass 98.079 g/mol
Appearance Clear, colorless liquid
Odor odorless
Density 1.8302 g/cm3, liquid[1]
Melting point 10.31[1] °C (50.56 °F; 283.46 K)
Boiling point 337[1] °C (639 °F; 610 K) When sulfuric acid is above 300 °C (572 °F; 573 K), it gradually decomposes to SO3 + H2O
miscible, exothermic
Vapor pressure 0.001 mmHg (20 °C)[2]
Acidity (pKa) -2.8±0.5[3], 1.99
Conjugate base Hydrogen sulfate
Viscosity 26.7 cP (20 °C)
Thermochemistry
157 J·mol−1·K−1[4]
Std enthalpy of
formation (ΔfH⦵298)
 −814 kJ·mol−1[4]
Hazards
Safety data sheet External MSDS
GHS pictograms
GHS Signal word Danger
GHS hazard statements
 H314
P260, P264, P280, P301+330+331, P303+361+353, P363, P304+340, P305+351+338, P310, P321, P405, P501
NFPA 704 (fire diamond)
Flash point Non-flammable
15 mg/m3 (IDLH), 1 mg/m3 (TWA), 2 mg/m3 (STEL)
Lethal dose or concentration (LD, LC):
2140 mg/kg (rat, oral)[5]
50 mg/m3 (guinea pig, 8 hr)
510 mg/m3 (rat, 2 hr)
320 mg/m3 (mouse, 2 hr)
18 mg/m3 (guinea pig)[5]
87 mg/m3 (guinea pig, 2.75 hr)[5]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 1 mg/m3[2]
REL (Recommended)
 TWA 1 mg/m3[2]
IDLH (Immediate danger)
 15 mg/m3[2]
Related compounds
Related strong acids
 Selenic acid
Hydrochloric acid
Nitric acid
Chromic acid
Related compounds
 Sulfurous acid
Peroxymonosulfuric acid
Sulfur trioxide
Oleum
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Its corrosiveness can be mainly ascribed to its strong acidic nature, and, if at a high concentration, its dehydrating properties. It is also hygroscopic, readily absorbing water vapor from the air.[6] Upon contact, sulfuric acid can cause severe chemical burns and even secondary thermal burns; it is very dangerous even at lower concentrations.[7][8]

Sulfuric acid is a very important commodity chemical, and a nation's sulfuric acid production is a good indicator of its industrial strength.[9] It is widely produced with different methods, such as contact process, wet sulfuric acid process, lead chamber process and some other methods.[10]

Sulfuric acid is also a key substance in the chemical industry. It is most commonly used in fertilizer manufacture,[11] but is also important in mineral processing, oil refining, wastewater processing, and chemical synthesis. It has a wide range of end applications including in domestic acidic drain cleaners,[12] as an electrolyte in lead-acid batteries, in dehydrating a compound, and in various cleaning agents.

Physical properties

Grades of sulfuric acid

Although nearly 100% sulfuric acid solutions can be made, the subsequent loss of SO
3 at the boiling point brings the concentration to 98.3% acid. The 98.3% grade is more stable in storage, and is the usual form of what is described as "concentrated sulfuric acid". Other concentrations are used for different purposes. Some common concentrations are:[13][14]

Mass fraction
H2SO4		 Density
(kg/L)		 Concentration
(mol/L)		 Common name
<29%1.00-1.25<4.2diluted sulfuric acid
29–32%1.25–1.284.2–5.0battery acid
(used in lead–acid batteries)
62–70%1.52–1.609.6–11.5chamber acid
fertilizer acid
78–80%1.70–1.7313.5–14.0tower acid
Glover acid
93.2%1.8317.466 °Bé ("66-degree Baumé") acid
98.3%1.8418.4concentrated sulfuric acid

"Chamber acid" and "tower acid" were the two concentrations of sulfuric acid produced by the lead chamber process, chamber acid being the acid produced in the lead chamber itself (<70% to avoid contamination with nitrosylsulfuric acid) and tower acid being the acid recovered from the bottom of the Glover tower.[13][14] They are now obsolete as commercial concentrations of sulfuric acid, although they may be prepared in the laboratory from concentrated sulfuric acid if needed. In particular, "10M" sulfuric acid (the modern equivalent of chamber acid, used in many titrations) is prepared by slowly adding 98% sulfuric acid to an equal volume of water, with good stirring: the temperature of the mixture can rise to 80 °C (176 °F) or higher.[14]

Sulfuric acid reacts with its anhydride, SO
3, to form H
2S
2O
7, called pyrosulfuric acid, fuming sulfuric acid, Disulfuric acid or oleum or, less commonly, Nordhausen acid. Concentrations of oleum are either expressed in terms of % SO
3 (called % oleum) or as % H
2SO
4 (the amount made if H
2O were added); common concentrations are 40% oleum (109% H
2SO
4) and 65% oleum (114.6% H
2SO
4). Pure H
2S
2O
7 is a solid with melting point of 36 °C.

Pure sulfuric acid has a vapor pressure of <0.001 mmHg at 25 °C and 1 mmHg at 145.8 °C,[15] and 98% sulfuric acid has a <1 mmHg vapor pressure at 40 °C.[16]

Pure sulfuric acid is a viscous clear liquid, like oil, and this explains the old name of the acid ('oil of vitriol').

Commercial sulfuric acid is sold in several different purity grades. Technical grade H
2SO
4 is impure and often colored, but is suitable for making fertilizer. Pure grades, such as United States Pharmacopeia (USP) grade, are used for making pharmaceuticals and dyestuffs. Analytical grades are also available.

Nine hydrates are known, but four of them were confirmed to be tetrahydrate (H2SO4·4H2O), hemihexahydrate (H2SO4·​6 1⁄2H2O) and octahydrate (H2SO4·8H2O).

Polarity and conductivity
Equilibrium of anhydrous sulfuric acid[17]
Species mMol/kg
HSO−
4		 15.0
H
3SO+
4		 11.3
H
3O+
 8.0
HS
2O−
7		 4.4
H
2S
2O
7		 3.6
H
2O		 0.1

Anhydrous H
2SO
4 is a very polar liquid, having a dielectric constant of around 100. It has a high electrical conductivity, caused by dissociation through protonating itself, a process known as autoprotolysis.[17]

2 H
2SO
4 ⇌ H
3SO+
4 + HSO−
4

The equilibrium constant for the autoprotolysis is[17]

Kap (25 °C) = [H
3SO+
4][HSO−
4] = 2.7×10−4

The comparable equilibrium constant for water, Kw is 10−14, a factor of 1010 (10 billion) smaller.

In spite of the viscosity of the acid, the effective conductivities of the H
3SO+
4 and HSO−
4 ions are high due to an intramolecular proton-switch mechanism (analogous to the Grotthuss mechanism in water), making sulfuric acid a good conductor of electricity. It is also an excellent solvent for many reactions.

Chemical properties

Reaction with water and dehydrating property
Drops of concentrated sulfuric acid rapidly decompose a piece of cotton towel by dehydration.

Because the hydration reaction of sulfuric acid is highly exothermic, dilution should always be performed by adding the acid to the water rather than the water to the acid.[18] Because the reaction is in an equilibrium that favors the rapid protonation of water, addition of acid to the water ensures that the acid is the limiting reagent. This reaction is best thought of as the formation of hydronium ions:

H
2SO
4 + H
2O → H
3O+
 + HSO−
4   Ka1 ≈ 103 (strong acid)
HSO−
4 + H
2O → H
3O+
 + SO2−
4   Ka2 = 1.0×10−2 [19]

HSO−
4 is the bisulfate anion and SO2−
4 is the sulfate anion. Ka1 and Ka2 are the acid dissociation constants.

Because the hydration of sulfuric acid is thermodynamically favorable and the affinity of it for water is sufficiently strong, sulfuric acid is an excellent dehydrating agent. Concentrated sulfuric acid has a very powerful dehydrating property, removing water (H2O) from other chemical compounds including sugar and other carbohydrates and producing carbon, heat, and steam.

In the laboratory, this is often demonstrated by mixing table sugar (sucrose) into sulfuric acid. The sugar changes from white to dark brown and then to black as carbon is formed. A rigid column of black, porous carbon will emerge as well. The carbon will smell strongly of caramel due to the heat generated.[20]

Similarly, mixing starch into concentrated sulfuric acid will give elemental carbon and water as absorbed by the sulfuric acid (which becomes slightly diluted). The effect of this can be seen when concentrated sulfuric acid is spilled on paper which is composed of cellulose; the cellulose reacts to give a burnt appearance, the carbon appears much as soot would in a fire. Although less dramatic, the action of the acid on cotton, even in diluted form, will destroy the fabric.

The reaction with copper(II) sulfate can also demonstrate the dehydration property of sulfuric acid. The blue crystal is changed into white powder as water is removed.

Acid-base properties

As an acid, sulfuric acid reacts with most bases to give the corresponding sulfate. For example, the blue copper salt copper(II) sulfate, commonly used for electroplating and as a fungicide, is prepared by the reaction of copper(II) oxide with sulfuric acid:

CuO (s) + H
2SO
4 (aq) → CuSO
4 (aq) + H
2O (l)

Sulfuric acid can also be used to displace weaker acids from their salts. Reaction with sodium acetate, for example, displaces acetic acid, CH
3COOH, and forms sodium bisulfate:

H
2SO
4 + CH
3COONa → NaHSO
4 + CH
3COOH

Similarly, reacting sulfuric acid with potassium nitrate can be used to produce nitric acid and a precipitate of potassium bisulfate. When combined with nitric acid, sulfuric acid acts both as an acid and a dehydrating agent, forming the nitronium ion NO+
2, which is important in nitration reactions involving electrophilic aromatic substitution. This type of reaction, where protonation occurs on an oxygen atom, is important in many organic chemistry reactions, such as Fischer esterification and dehydration of alcohols.

Solid state structure of the [D3SO4]+ ion present in [D3SO4]+[SbF6]−, synthesized by using DF in place of HF. (see text)

When allowed to react with superacids, sulfuric acid can act as a base and be protonated, forming the [H3SO4]+ ion. Salt of [H3SO4]+ have been prepared using the following reaction in liquid HF:

((CH3)3SiO)2SO2 + 3 HF + SbF5 → [H3SO4]+[SbF6]− + 2 (CH3)3SiF

The above reaction is thermodynamically favored due to the high bond enthalpy of the Si–F bond in the side product. Protonation using simply HF/SbF5, however, have met with failure, as pure sulfuric acid undergoes self-ionization to give [H3O]+ ions, which prevents the conversion of H2SO4 to [H3SO4]+ by the HF/SbF5 system:[21]

2 H2SO4 ⇌ [H3O]+ + [HS2O7]−

Reactions with metals

Even dilute sulfuric acid reacts with many metals via a single displacement reaction as with other typical acids, producing hydrogen gas and salts (the metal sulfate). It attacks reactive metals (metals at positions above copper in the reactivity series) such as iron, aluminium, zinc, manganese, magnesium, and nickel.

Fe + H
2SO
4 → H
2 + FeSO
4

Concentrated sulfuric acid can serve as an oxidizing agent, releasing sulfur dioxide:[7]

Cu + 2 H2SO4 → SO2 + 2 H2O + SO2−
4 + Cu2+

Lead and tungsten, however, are resistant to sulfuric acid.

Reactions with carbon

Hot concentrated sulfuric acid oxidizes carbon[22] (as bituminous coal) and sulfur.

C + 2 H2SO4 → CO2 + 2 SO2 + 2 H2O
S + 2 H2SO4 → 3 SO2 + 2 H2O

Reaction with sodium chloride

It reacts with sodium chloride, and gives hydrogen chloride gas and sodium bisulfate:

NaCl + H2SO4 → NaHSO4 + HCl

Electrophilic aromatic substitution

Benzene undergoes electrophilic aromatic substitution with sulfuric acid to give the corresponding sulfonic acids:[23]

Occurrence
Rio Tinto with its highly acidic water

Pure sulfuric acid is not encountered naturally on Earth in anhydrous form, due to its great affinity for water. Dilute sulfuric acid is a constituent of acid rain, which is formed by atmospheric oxidation of sulfur dioxide in the presence of water – i.e., oxidation of sulfurous acid. When sulfur-containing fuels such as coal or oil are burned, sulfur dioxide is the main byproduct (besides the chief products carbon oxides and water).

Sulfuric acid is formed naturally by the oxidation of sulfide minerals, such as iron sulfide. The resulting water can be highly acidic and is called acid mine drainage (AMD) or acid rock drainage (ARD). This acidic water is capable of dissolving metals present in sulfide ores, which results in brightly colored, toxic solutions. The oxidation of pyrite (iron sulfide) by molecular oxygen produces iron(II), or Fe2+
:

2 FeS
2 (s) + 7 O
2 + 2 H
2O → 2 Fe2+
 + 4 SO2−
4 + 4 H+

The Fe2+
 can be further oxidized to Fe3+
:

4 Fe2+
 + O
2 + 4 H+
 → 4 Fe3+
 + 2 H
2O

The Fe3+
 produced can be precipitated as the hydroxide or hydrous iron oxide:

Fe3+
 + 3 H
2O → Fe(OH)
3↓ + 3 H+

The iron(III) ion ("ferric iron") can also oxidize pyrite:

FeS
2(s) + 14 Fe3+
 + 8 H
2O → 15 Fe2+
 + 2 SO2−
4 + 16 H+

When iron(III) oxidation of pyrite occurs, the process can become rapid. pH values below zero have been measured in ARD produced by this process.

ARD can also produce sulfuric acid at a slower rate, so that the acid neutralizing capacity (ANC) of the aquifer can neutralize the produced acid. In such cases, the total dissolved solids (TDS) concentration of the water can be increased from the dissolution of minerals from the acid-neutralization reaction with the minerals.

Sulfuric acid is used as a defense by certain marine species, for example, the phaeophyte alga Desmarestia munda (order Desmarestiales) concentrates sulfuric acid in cell vacuoles.[24]

Stratospheric aerosol

In the stratosphere, the atmosphere's second layer that is generally between 10 and 50 km above Earth's surface, sulfuric acid is formed by the oxidation of volcanic sulfur dioxide by the hydroxyl radical:[25]

SO
2 + HO• → HSO
3
HSO
3 + O
2 → SO
3 + HO
2
SO
3 + H
2O → H
2SO
4

Because sulfuric acid reaches supersaturation in the stratosphere, it can nucleate aerosol particles and provide a surface for aerosol growth via condensation and coagulation with other water-sulfuric acid aerosols. This results in the stratospheric aerosol layer.[25]

Extraterrestrial sulfuric acid

The permanent Venusian clouds produce a concentrated acid rain, as the clouds in the atmosphere of Earth produce water rain.[26] Jupiter's moon Europa is also thought to have an atmosphere containing sulfuric acid hydrates.[27]

Manufacture
Main articles: Contact process, Wet sulfuric acid process, and Lead chamber process

Sulfuric acid is produced from sulfur, oxygen and water via the conventional contact process (DCDA) or the wet sulfuric acid process (WSA).

Contact process
Main article: Contact process

In the first step, sulfur is burned to produce sulfur dioxide.

S (s) + O
2 → SO
2

The sulfur dioxide is oxidized to sulfur trioxide by oxygen in the presence of a vanadium(V) oxide catalyst. This reaction is reversible and the formation of the sulfur trioxide is exothermic.

2 SO
2 + O
2 ⇌ 2 SO
3

The sulfur trioxide is absorbed into 97–98% H
2SO
4 to form oleum (H
2S
2O
7), also known as fuming sulfuric acid. The oleum is then diluted with water to form concentrated sulfuric acid.

H
2SO
4 + SO
3 → H
2S
2O
7
H
2S
2O
7 + H
2O → 2 H
2SO
4

Directly dissolving SO
3 in water is not practiced.

Wet sulfuric acid process
Main article: Wet sulfuric acid process

In the first step, sulfur is burned to produce sulfur dioxide:

S + O
2 → SO
2

or, alternatively, hydrogen sulfide (H
2S) gas is incinerated to SO
2 gas:

2 H
2S + 3 O
2 → 2 H
2O + 2 SO
2 (−518 kJ/mol)

The sulfur dioxide then oxidized to sulfur trioxide using oxygen with vanadium(V) oxide as catalyst.

2 SO
2 + O
2 ⇌ 2 SO
3 (−99 kJ/mol) (reaction is reversible)

The sulfur trioxide is hydrated into sulfuric acid H
2SO
4:

SO
3 + H
2O → H
2SO
4(g) (−101 kJ/mol)

The last step is the condensation of the sulfuric acid to liquid 97–98% H
2SO
4:

H
2SO
4(g) → H
2SO
4(l) (−69 kJ/mol)

Other methods

Another method is the less well-known metabisulfite method, in which metabisulfite is placed at the bottom of a beaker, and 12.6 molar concentration hydrochloric acid is added. The resulting gas is bubbled through nitric acid, which will release brown/red vapors. The completion of the reaction is indicated by the ceasing of the fumes. This method does not produce an inseparable mist, which is quite convenient.

SO2 + HNO3 + H2O → H2SO4 + NO

In principle, sulfuric acid can be produced in the laboratory by burning sulfur in air followed by dissolving the resulting sulfur dioxide in a hydrogen peroxide solution.

SO2 + H2O2 → H2SO4

Alternatively, dissolving sulfur dioxide in an aqueous solution of a certain oxidizing metal salt such as copper (II) or iron (III) chloride:

2FeCl3 + 2H2O + SO2 → 2FeCl2 + H2SO4 + 2HCl
2CuCl2 + 2H2O + SO2 → 2CuCl + H2SO4 + 2HCl

Two less well-known laboratory methods of producing sulfuric acid, albeit in dilute form and require some extra effort in purification. A solution of copper (II) sulfate can be electrolyzed with a copper cathode and platinum/graphite anode to give spongy copper at cathode and evolution of oxygen gas at anode, the solution diluted sulfuric acid that indicates completed reaction when it turns from blue to clear (production of hydrogen at cathode is another sign):

2CuSO4 + 2H2O → 2Cu + 2H2SO4 + O2

More costly, dangerous, and troublesome yet novel is the electrobromine method, which employs a mixture of sulfur, water, and hydrobromic acid as the electrolytic solution. The sulfur pushed to bottom of container under the acid solution, then copper cathode and platinum/graphite anode are used with cathode near surface and anode at bottom of electrolyte to apply the current. This may take longer and emits toxic bromine/sulfur bromide vapors, but reactant acid is recyclable, overall only sulfur and water converted to sulfuric acid (omitting losses of acid as vapors):

2HBr → H2 + Br2 (electrolysis of aqueous hydrogen bromide)
Br2 + Br− ↔ Br3− (initial tribromide production, eventually reverses as Br− depletes)
2S + Br2 → S2Br2 (bromine reacts with sulfur to form disulfur dibromide)
S2Br2 + 8H2O + 5Br2 → 2H2SO4 + 12HBr (oxidation and hydration of disulfur dibromide)

Prior to 1900, most sulfuric acid was manufactured by the lead chamber process.[28] As late as 1940, up to 50% of sulfuric acid manufactured in the United States was produced by chamber process plants.

In early to mid nineteenth century "vitriol" plants existed, among other places, in Prestonpans in Scotland, Shropshire and the Lagan Valley in County Antrim Ireland where it was used as a bleach for linen. Early bleaching of linen was done using lactic acid from sour milk but this was a slow process and the use of vitriol sped up the bleaching process.[29]

Uses
Sulfuric acid production in 2000

Sulfuric acid is a very important commodity chemical, and indeed, a nation's sulfuric acid production is a good indicator of its industrial strength.[9] World production in the year 2004 was about 180 million tonnes, with the following geographic distribution: Asia 35%, North America (including Mexico) 24%, Africa 11%, Western Europe 10%, Eastern Europe and Russia 10%, Australia and Oceania 7%, South America 7%.[30] Most of this amount (≈60%) is consumed for fertilizers, particularly superphosphates, ammonium phosphate and ammonium sulfates. About 20% is used in chemical industry for production of detergents, synthetic resins, dyestuffs, pharmaceuticals, petroleum catalysts, insecticides and antifreeze, as well as in various processes such as oil well acidicizing, aluminium reduction, paper sizing, water treatment. About 6% of uses are related to pigments and include paints, enamels, printing inks, coated fabrics and paper, and the rest is dispersed into a multitude of applications such as production of explosives, cellophane, acetate and viscose textiles, lubricants, non-ferrous metals, and batteries.[31]

Industrial production of chemicals

The major use for sulfuric acid is in the "wet method" for the production of phosphoric acid, used for manufacture of phosphate fertilizers. In this method, phosphate rock is used, and more than 100 million tonnes are processed annually. This raw material is shown below as fluorapatite, though the exact composition may vary. This is treated with 93% sulfuric acid to produce calcium sulfate, hydrogen fluoride (HF) and phosphoric acid. The HF is removed as hydrofluoric acid. The overall process can be represented as:

Ammonium sulfate, an important nitrogen fertilizer, is most commonly produced as a byproduct from coking plants supplying the iron and steel making plants. Reacting the ammonia produced in the thermal decomposition of coal with waste sulfuric acid allows the ammonia to be crystallized out as a salt (often brown because of iron contamination) and sold into the agro-chemicals industry.

Another important use for sulfuric acid is for the manufacture of aluminium sulfate, also known as paper maker's alum. This can react with small amounts of soap on paper pulp fibers to give gelatinous aluminium carboxylates, which help to coagulate the pulp fibers into a hard paper surface. It is also used for making aluminium hydroxide, which is used at water treatment plants to filter out impurities, as well as to improve the taste of the water. Aluminium sulfate is made by reacting bauxite with sulfuric acid:

2 AlO(OH) + 3 H
2SO
4 → Al
2(SO
4)
3 + 4 H
2O

Sulfuric acid is also important in the manufacture of dyestuffs solutions.

Sulfur–iodine cycle

The sulfur–iodine cycle is a series of thermo-chemical processes possibly usable to produce hydrogen from water. It consists of three chemical reactions whose net reactant is water and whose net products are hydrogen and oxygen.

2 I
2 + 2 SO
2 + 4 H
2O → 4 HI + 2 H
2SO
4		   (120 °C , Bunsen reaction)
2 H
2SO
4 → 2 SO
2 + 2 H
2O + O
2		   (830 °C)
4 HI → 2 I
2 + 2 H
2		   (320 °C)

The compounds of sulfur and iodine are recovered and reused, hence the consideration of the process as a cycle. This process is endothermic and must occur at high temperatures, so energy in the form of heat has to be supplied.

The sulfur–iodine cycle has been proposed as a way to supply hydrogen for a hydrogen-based economy. It is an alternative to electrolysis, and does not require hydrocarbons like current methods of steam reforming. But note that all of the available energy in the hydrogen so produced is supplied by the heat used to make it.

The sulfur–iodine cycle is currently being researched as a feasible method of obtaining hydrogen, but the concentrated, corrosive acid at high temperatures poses currently insurmountable safety hazards if the process were built on a large scale.[32][33]

Industrial cleaning agent
Main article: Cleaning agent

Sulfuric acid is used in large quantities by the iron and steelmaking industry to remove oxidation, rust, and scaling from rolled sheet and billets prior to sale to the automobile and major appliances industry. Used acid is often recycled using a spent acid regeneration (SAR) plant. These plants combust spent acid with natural gas, refinery gas, fuel oil or other fuel sources. This combustion process produces gaseous sulfur dioxide (SO
2) and sulfur trioxide (SO
3) which are then used to manufacture "new" sulfuric acid. SAR plants are common additions to metal smelting plants, oil refineries, and other industries where sulfuric acid is consumed in bulk, as operating a SAR plant is much cheaper than the recurring costs of spent acid disposal and new acid purchases.

Hydrogen peroxide (H
2O
2) can be added to sulfuric acid to produce piranha solution, a powerful but very toxic cleaning solution with which substrate surfaces can be cleaned. Piranha solution is typically used in the microelectronics industry, and also in laboratory settings to clean glassware.

Catalyst

Sulfuric acid is used for a variety of other purposes in the chemical industry. For example, it is the usual acid catalyst for the conversion of cyclohexanone oxime to caprolactam, used for making nylon. It is used for making hydrochloric acid from salt via the Mannheim process. Much H
2SO
4 is used in petroleum refining, for example as a catalyst for the reaction of isobutane with isobutylene to give isooctane, a compound that raises the octane rating of gasoline (petrol). Sulfuric acid is also often used as a dehydrating or oxidising agent in industrial reactions, such as the dehydration of various sugars to form solid carbon.

Electrolyte
Acidic drain cleaners usually contain sulfuric acid at a high concentration which turns a piece of pH paper red and chars it instantly, demonstrating both the strong acidic nature and dehydrating property.

Sulfuric acid acts as the electrolyte in lead–acid batteries (lead-acid accumulator):

At anode:

Pb + SO
42− ⇌ PbSO
4 + 2 e−

At cathode:

PbO
2 + 4 H+ + SO
42− + 2 e− ⇌ PbSO
4 + 2 H2O
An acidic drain cleaner can be used to dissolve grease, hair and even tissue paper inside water pipes.

Overall:

Pb + PbO
2 + 4 H+ + 2 SO
42− ⇌ 2 PbSO
4 + 2 H2O

Domestic uses

Sulfuric acid at high concentrations is frequently the major ingredient in acidic drain cleaners[12] which are used to remove grease, hair, tissue paper, etc. Similar to their alkaline versions, such drain openers can dissolve fats and proteins via hydrolysis. Moreover, as concentrated sulfuric acid has a strong dehydrating property, it can remove tissue paper via dehydrating process as well. Since the acid may react with water vigorously, such acidic drain openers should be added slowly into the pipe to be cleaned.

History
John Dalton's 1808 sulfuric acid molecule shows a central sulfur atom bonded to three oxygen atoms, or sulfur trioxide, the anhydride of sulfuric acid.

The study of vitriol, a category of glassy minerals from which the acid can be derived, began in ancient times. Sumerians had a list of types of vitriol that they classified according to the substances' color. Some of the earliest discussions on the origin and properties of vitriol is in the works of the Greek physician Dioscorides (first century AD) and the Roman naturalist Pliny the Elder (23–79 AD). Galen also discussed its medical use. Metallurgical uses for vitriolic substances were recorded in the Hellenistic alchemical works of Zosimos of Panopolis, in the treatise Phisica et Mystica, and the Leyden papyrus X.[34]

Medieval Islamic era alchemists, Jābir ibn Hayyān (c. 721 – c. 815 AD, also known as Geber), Muhammad ibn Zakariya al-Razi (865 – 925 AD), and Jamal Din al-Watwat (d. 1318, wrote the book Mabāhij al-fikar wa-manāhij al-'ibar), included vitriol in their mineral classification lists. Ibn Sina focused on its medical uses and different varieties of vitriol.[34] Razi is credited with being the first to produce sulfuric acid.[35][36]

Sulfuric acid was called "oil of vitriol" by medieval European alchemists because it was prepared by roasting "green vitriol" (iron(II) sulfate) in an iron retort. There are references to it in the works of Vincent of Beauvais and in the Compositum de Compositis ascribed to Saint Albertus Magnus. A passage from Pseudo-Geber's Summa Perfectionis was long considered to be a recipe for sulfuric acid, but this was a misinterpretation.[34]

In the seventeenth century, the German-Dutch chemist Johann Glauber prepared sulfuric acid by burning sulfur together with saltpeter (potassium nitrate, KNO
3), in the presence of steam. As saltpeter decomposes, it oxidizes the sulfur to SO
3, which combines with water to produce sulfuric acid. In 1736, Joshua Ward, a London pharmacist, used this method to begin the first large-scale production of sulfuric acid.

In 1746 in Birmingham, John Roebuck adapted this method to produce sulfuric acid in lead-lined chambers, which were stronger, less expensive, and could be made larger than the previously used glass containers. This process allowed the effective industrialization of sulfuric acid production. After several refinements, this method, called the lead chamber process or "chamber process", remained the standard for sulfuric acid production for almost two centuries.[4]

Sulfuric acid created by John Roebuck's process approached a 65% concentration. Later refinements to the lead chamber process by French chemist Joseph Louis Gay-Lussac and British chemist John Glover improved concentration to 78%. However, the manufacture of some dyes and other chemical processes require a more concentrated product. Throughout the 18th century, this could only be made by dry distilling minerals in a technique similar to the original alchemical processes. Pyrite (iron disulfide, FeS
2) was heated in air to yield iron(II) sulfate, FeSO
4, which was oxidized by further heating in air to form iron(III) sulfate, Fe2(SO4)3, which, when heated to 480 °C, decomposed to iron(III) oxide and sulfur trioxide, which could be passed through water to yield sulfuric acid in any concentration. However, the expense of this process prevented the large-scale use of concentrated sulfuric acid.[4]

In 1831, British vinegar merchant Peregrine Phillips patented the contact process, which was a far more economical process for producing sulfur trioxide and concentrated sulfuric acid. Today, nearly all of the world's sulfuric acid is produced using this method.[37]

Safety

Laboratory hazards
Drops of 98% sulfuric acid char a piece of tissue paper instantly. Carbon is left after the dehydration reaction staining the paper black.

Sulfuric acid is capable of causing very severe burns, especially when it is at high concentrations. In common with other corrosive acids and alkali, it readily decomposes proteins and lipids through amide and ester hydrolysis upon contact with living tissues, such as skin and flesh. In addition, it exhibits a strong dehydrating property on carbohydrates, liberating extra heat and causing secondary thermal burns.[7][8] Accordingly, it rapidly attacks the cornea and can induce permanent blindness if splashed onto eyes. If ingested, it damages internal organs irreversibly and may even be fatal.[6] Protective equipment should hence always be used when handling it. Moreover, its strong oxidizing property makes it highly corrosive to many metals and may extend its destruction on other materials.[7] Because of such reasons, damage posed by sulfuric acid is potentially more severe than that by other comparable strong acids, such as hydrochloric acid and nitric acid.

Sulfuric acid must be stored carefully in containers made of nonreactive material (such as glass). Solutions equal to or stronger than 1.5 M are labeled "CORROSIVE", while solutions greater than 0.5 M but less than 1.5 M are labeled "IRRITANT". However, even the normal laboratory "dilute" grade (approximately 1 M, 10%) will char paper if left in contact for a sufficient time.

The standard first aid treatment for acid spills on the skin is, as for other corrosive agents, irrigation with large quantities of water. Washing is continued for at least ten to fifteen minutes to cool the tissue surrounding the acid burn and to prevent secondary damage. Contaminated clothing is removed immediately and the underlying skin washed thoroughly.

Dilution hazards

Preparation of the diluted acid can be dangerous due to the heat released in the dilution process. To avoid splattering, the concentrated acid is usually added to water and not the other way around. Water has a higher heat capacity than the acid, and so a vessel of cold water will absorb heat as acid is added.

Comparison of sulfuric acid and water
Physical property H2SO4 Water Units
Density 1.84 1.0 kg/L
Volumetric heat capacity 2.54 4.18 kJ/L
Boiling point 337 100 °C

Also, because the acid is denser than water, it sinks to the bottom. Heat is generated at the interface between acid and water, which is at the bottom of the vessel. Acid will not boil, because of its higher boiling point. Warm water near the interface rises due to convection, which cools the interface, and prevents boiling of either acid or water.

In contrast, addition of water to concentrated sulfuric acid results in a thin layer of water on top of the acid. Heat generated in this thin layer of water can boil, leading to the dispersal of a sulfuric acid aerosol or worse, an explosion.

Preparation of solutions greater than 6 M (35%) in concentration is most dangerous, because the heat produced may be sufficient to boil the diluted acid: efficient mechanical stirring and external cooling (such as an ice bath) are essential.

Reaction rates double for about every 10-degree Celsius increase in temperature.[38] Therefore, the reaction will become more violent as dilution proceeds, unless the mixture is given time to cool. Adding acid to warm water will cause a violent reaction.

On a laboratory scale, sulfuric acid can be diluted by pouring concentrated acid onto crushed ice made from de-ionized water. The ice melts in an endothermic process while dissolving the acid. The amount of heat needed to melt the ice in this process is greater than the amount of heat evolved by dissolving the acid so the solution remains cold. After all the ice has melted, further dilution can take place using water.

Industrial hazards

Sulfuric acid is non-flammable.

The main occupational risks posed by this acid are skin contact leading to burns (see above) and the inhalation of aerosols. Exposure to aerosols at high concentrations leads to immediate and severe irritation of the eyes, respiratory tract and mucous membranes: this ceases rapidly after exposure, although there is a risk of subsequent pulmonary edema if tissue damage has been more severe. At lower concentrations, the most commonly reported symptom of chronic exposure to sulfuric acid aerosols is erosion of the teeth, found in virtually all studies: indications of possible chronic damage to the respiratory tract are inconclusive as of 1997. Repeated occupational exposure to sulfuric acid mists may increase the chance of lung cancer by up to 64 percent.[39] In the United States, the permissible exposure limit (PEL) for sulfuric acid is fixed at 1 mg/m3: limits in other countries are similar. There have been reports of sulfuric acid ingestion leading to vitamin B12 deficiency with subacute combined degeneration. The spinal cord is most often affected in such cases, but the optic nerves may show demyelination, loss of axons and gliosis.

International commerce of sulfuric acid is controlled under the United Nations Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances, 1988, which lists sulfuric acid under Table II of the convention as a chemical frequently used in the illicit manufacture of narcotic drugs or psychotropic substances.[40]

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See also

References
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  2. NIOSH Pocket Guide to Chemical Hazards. "#0577". National Institute for Occupational Safety and Health (NIOSH).
  3. Guthrie, J. Peter (1978), Hydrolysis of esters of oxy acids: pKa values for strong acids; Brflnsted relationship for attack of water at methyl; free energies of hydrolysis of esters of oxy acids; and a linear relationship between free energy of hydrolysis and pKa holding over a range of 20 pK units, E. Can. J. Chem, retrieved 7 August 2020
  4. Zumdahl, Steven S. (2009). Chemical Principles 6th Ed. Houghton Mifflin Company. p. A23. ISBN 978-0-618-94690-7.
  5. "Sulfuric acid". Immediately Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  6. "Sulfuric acid safety data sheet" (PDF). arkema-inc.com. Archived from the original (PDF) on 17 June 2012. Clear to turbid oily odorless liquid, colorless to slightly yellow.
  7. "Sulfuric acid – uses". dynamicscience.com.au. Archived from the original on 9 May 2013.
  8. "BASF Chemical Emergency Medical Guidelines – Sulfuric acid (H2SO4)" (PDF). BASF Chemical Company. 2012. Archived from the original (PDF) on 14 June 2019. Retrieved 18 December 2014.
  9. Chenier, Philip J. (1987). Survey of Industrial Chemistry. New York: John Wiley & Sons. pp. 45–57. ISBN 978-0-471-01077-7.
  10. Hermann Müller "Sulfuric Acid and Sulfur Trioxide" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim. 2000 doi:10.1002/14356007.a25_635
  11. "Sulfuric acid".
  12. "Sulphuric acid drain cleaner" (PDF). herchem.com. Archived from the original (PDF) on 29 October 2013.
  13. "Sulfuric Acid". The Columbia Encyclopedia (6th ed.). 2009. Retrieved 16 March 2010.
  14. "Sulphuric acid". Encyclopædia Britannica. 26 (11th ed.). 1910–1911. pp. 65–69.
  15. "Sulfuric acid" (PDF). Determination of Noncancer Chronic Reference Exposure Levels Batch 2B December 2001. 2001. Retrieved 1 October 2012.
  16. "Sulfuric Acid 98%" (PDF). rhodia.com. 2009. Archived from the original (PDF) on 7 January 2011. Retrieved 2 July 2014.
  17. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  18. Consortium of Local Education Authorities for the Provision of Science Equipment -STUDENT SAFETY SHEETS 22 Sulfuric(VI) acid
  19. "Ionization Constants of Inorganic Acids". .chemistry.msu.edu. Retrieved 30 May 2011.
  20. sulfuric acid on sugar cubes chemistry experiment 8. Old Version. YouTube. Retrieved on 18 July 2011.
  21. Housecroft, Catherine E.; Sharpe, Alan G. (2008). "Chapter 16: The group 16 elements". Inorganic Chemistry, 3rd Edition. Pearson. p. 523. ISBN 978-0-13-175553-6.
  22. Kinney, Corliss Robert; Grey, V. E. (1959). Reactions of a Bituminous Coal with Sulfuric Acid (PDF). Pennsylvania State University. Archived from the original (PDF) on 28 April 2017.
  23. Carey, F. A. "Reactions of Arenes. Electrophilic Aromatic Substitution". On-Line Learning Center for Organic Chemistry. University of Calgary. Archived from the original on 6 July 2008. Retrieved 27 January 2008.CS1 maint: unfit url (link)
  24. Pelletreau, K.; Muller-Parker, G. (2002). "Sulfuric acid in the phaeophyte alga Desmarestia munda deters feeding by the sea urchin Strongylocentrotus droebachiensis". Marine Biology. 141 (1): 1–9. doi:10.1007/s00227-002-0809-6.
  25. Kremser, S.; Thomson, L.W. (2016). "Stratospheric aerosol—Observations, processes, and impact on climate" (PDF). Reviews of Geophysics. 54 (2): 278–335. Bibcode:2016RvGeo..54..278K. doi:10.1002/2015RG000511.
  26. Krasnopolsky, Vladimir A. (2006). "Chemical composition of Venus atmosphere and clouds: Some unsolved problems". Planetary and Space Science. 54 (13–14): 1352–1359. Bibcode:2006P&SS...54.1352K. doi:10.1016/j.pss.2006.04.019.
  27. Orlando, T. M.; McCord, T. B.; Grieves, G. A. (2005). "The chemical nature of Europa surface material and the relation to a subsurface ocean". Icarus. 177 (2): 528–533. Bibcode:2005Icar..177..528O. doi:10.1016/j.icarus.2005.05.009.
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  29. (Harm), Benninga, H. (1990). A history of lactic acid making: a chapter in the history of biotechnology. Dordrecht [Netherland]: Kluwer Academic Publishers. p. 4. ISBN 9780792306252. OCLC 20852966.
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  31. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 653. ISBN 978-0-08-037941-8.
  32. Ngo, Christian; Natowitz, Joseph (2016). Our Energy Future: Resources, Alternatives and the Environment. John Wiley & Sons. pp. 418–419. ISBN 9781119213369.
  33. https://www.hydrogen.energy.gov/pdfs/review05/pd27_pickard.pdf
  34. Karpenko, Vladimir and Norris, John A. (2001). Vitriol in the history of Chemistry, Charles University
  35. Modanlou, Houchang D. (November 2008). "A tribute to Zakariya Razi (865 – 925 AD), an Iranian pioneer scholar" (PDF). Archives of Iranian Medicine. 11 (6): 673–677. PMID 18976043. Retrieved 17 May 2018. Abu Bakr Mohammad Ibn Zakariya al-Razi, known in the West as Rhazes, was born in 865 AD in the ancient city of Rey, Near Tehran. A musician during his youth he became an alchemist. He discovered alcohol and sulfuric acid. He classified substances as plants, organic, and inorganic.
  36. Schlosser, Stefan (May 2011). "Distillation – from Bronze Age till today". Retrieved 17 May 2018. Al-Razi (865–925) was the preeminent Pharmacist and physician of his time [5]. The discovery of alcohol, first to produce acids such as sulfuric acid, writing up extensive notes on diseases such as smallpox and chickenpox, a pioneer in ophthalmology, author of first book on pediatrics, making leading contributions in inorganic and organic chemistry, also the author of several philosophical works. Cite journal requires |journal= (help)
  37. Philip J. Chenier (1 April 2002). Survey of industrial chemistry. Springer. pp. 28–. ISBN 978-0-306-47246-6. Retrieved 23 December 2011.
  38. Pauling, L.C. (1988) General Chemistry, Dover Publications
  39. Beaumont, JJ; Leveton, J; Knox, K; Bloom, T; McQuiston, T; Young, M; Goldsmith, R; Steenland, NK; Brown, DP; Halperin, WE (1987). "Lung cancer mortality in workers exposed to sulfuric acid mist and other acid mists". J Natl Cancer Inst. 79 (5): 911–21. doi:10.1093/jnci/79.5.911. PMID 3479642.
  40. Annex to Form D ("Red List"), 11th Edition, January 2007 (p. 4). International Narcotics Control Board. Vienna, Austria.
Compounds containing the sulfate group (SO2−
4)
H2SO4 He
Li2SO4 BeSO4 B esters
ROSO3−
(RO)2SO2		 (NH4)2SO4
[N2H5]HSO4
(NH3OH)2SO4
NOHSO4		 HOSO4 F Ne
Na2SO4
NaHSO4		 MgSO4 Al2(SO4)3
Al2SO4(OAc)4		 Si P SO42−
HSO3HSO4
(HSO4)2		 Cl Ar
K2SO4
KHSO4		 CaSO4 Sc2(SO4)3 TiOSO4 VSO4
V2(SO4)3
VOSO4		 CrSO4
Cr2(SO4)3		 MnSO4 FeSO4
Fe2(SO4)3		 CoSO4
Co2(SO4)3		 NiSO4
Ni2(SO4)3		 CuSO4
Cu2SO4
[Cu(NH3)4(H2O)]SO4		 ZnSO4 Ga2(SO4)3 Ge As Se Br Kr
RbHSO4
Rb2SO4		 SrSO4 Y2(SO4)3 Zr(SO4)2 Nb MoSO4
Mo2(SO4)3
Mo(SO4)2
Mo(SO4)2
Mo(SO4)3		 Tc Ru(SO4)2 RhSO4
Rh2(SO4)3		 PdSO4 Ag2SO4
AgSO4		 CdSO4 In2(SO4)3 SnSO4
Sn(SO4)2		 Sb2(SO4)3 Te I Xe
Cs2SO4
CsHSO4		 BaSO4   Hf Ta W Re OsSO4
Os2(SO4)3
Os(SO4)2		 IrSO4
Ir2(SO4)3		 PtSO4
Pt(SO4)2		 AuSO4
Au2(SO4)3		 Hg2SO4
HgSO4		 Tl2SO4
Tl2(SO4)3		 PbSO4
Pb(SO4)2		 Bi2(SO4)3 PoSO4
Po(SO4)2		 At Rn
Fr Ra   Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
↓
La2(SO4)3 Ce2(SO4)3
Ce(SO4)2		 Pr2(SO4)3 Nd2(SO4)3 Pm2(SO4)3 Sm2(SO4)3 Eu2(SO4)3 Gd2(SO4)3 Tb2(SO4)3 Dy2(SO4)3 Ho2(SO4)3 Er2(SO4)3 Tm2(SO4)3 Yb2(SO4)3 Lu2(SO4)3
Ac2(SO4)3 Th(SO4)2 Pa U2(SO4)3
U(SO4)2
UO2SO4		 Np(SO4)2 Pu(SO4)2 Am2(SO4)3 Cm2(SO4)3 Bk Cf Es Fm Md No Lr
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