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{{Chembox new| Name = Sulfuric acid| ImageFile = Sulfuric-acid-2D-dimensions.svg| ImageFile1 = Sulfuric-acid-3D-vdW.png| IUPACName = Sulfuric Acid| OtherNames = oil of vitriol| Section1 = {{Chembox Identifiers| CASNo = 7664-93-9| RTECS = WS5600000 -->
| Section2 = {{Chembox Properties| Formula = H2SO4 (aq)| MolarMass = 98.07848 g mol−1| Appearance = clear, colorless,odorless liquid| Density = 1.84 g cm−3, liquid| Solubility = fully miscible
(exothermic)| MeltingPt = 10 °C (283 K)| BoilingPt = 338 °C (611 K)| Viscosity = 26.7 c
Poise at 20°C -->
| Section7 = {{Chembox Hazards| FlashPt = Non-flammable| EUClass = Corrosive (
C)| NFPA-H = 3| NFPA-F = 0| NFPA-R = 2| NFPA-O = COR| RPhrases = | SPhrases = , , , -->
| Section8 = {{Chembox Related| Function =
strong acids]
Hydrochloric acidNitric acid
[Sulfurous acidPeroxymonosulfuric acid
Sulfur trioxide
Oleum-->-->
Sulfuric (or sulphuric) acid,
hydrogen2
sulfuroxygen4, is a strong
mineral acid. It is soluble in
water at all concentrations. It was once known as
oil of vitriol, coined by the 8th-century Alchemy (Islam) Geber (Geber) after his discovery of the chemical.Khairallah, Amin A.
Outline of Arabic Contributions to Medicine, chapter 10. Beirut, 1946. Sulfuric acid has many applications, and is one of the top products of the chemical industry. World production in 2001 was 165 million
tonnes, with an approximate value of US$8 billion. Principal uses include ore processing, fertilizer manufacturing, Oil refinery,
wastewater processing, and chemical synthesis.
Many
proteins are made of
sulfur-containing amino
acids (such as
cysteine and methionine) which produce sulfuric acid when
metabolism by the body.
Manufacture
Sulfuric acid is produced from sulfur,
oxygen and
water via the contact process.
In the first step,
sulfur is burned to produce sulfur dioxide.
(1) (
Solid) + Oxygen(Gas) → Sulfur dioxide(g)
This is then oxidised to sulfur trioxide using oxygen in the presence of a
vanadium(V) oxide catalyst.
(2) 2 SO2 + O2(g) →
Sulfur trioxide(g) (in presence of
Vanadium pentoxide)
Finally the sulfur trioxide is treated with water (usually as 97-98% H2SO4 containing 2-3% water) to produce 98-99% sulfuric acid.
(3) SO3(g) +
Water (molecule)(
liquid) → H2SO4(l)
Note that directly dissolving SO3 in water is impractical due to the highly exothermic nature of the reaction. Mists are formed instead of a liquid.Alternatively, SO3 can be absorbed into H2SO4 to produce
oleum (H2S2O7), which may then be mixed with water to form sulfuric acid.
(3) H2SO4
(liquid) + SO3 → H2S2O7
(l)
Oleum is reacted with water to form concentrated H2SO4.
(4) H2S2O7
(l) + H2O
(l) → 2 H2SO4
(l)
In 1993, American production of sulfuric acid amounted to 36.4 million tonnes. World production in 2001 was 165 million tonnes.
Physical properties
Forms of sulfuric acid
Although nearly 100% sulfuric acid can be made, this loses sulfur trioxide at the boiling point to produce 98.3% acid. The 98% 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
- 10%, dilute sulfuric acid for laboratory use,
- 33.5%, battery acid (used in lead-acid battery),
- 62.18%, chamber or fertilizer acid,
- 77.67%, tower or Glover acid,
- 98%, concentrated acid.
Different purities are also available. Technical grade H2SO4 is impure and often colored, but is suitable for making fertilizer. Pure grades such as US
Pharmacopoeia (USP) grade are used for making
pharmaceuticals and dyestuffs.
When high concentrations of SO3
(gas) are added to sulfuric acid, H2S2O7, called
pyrosulfuric acid,
fuming sulfuric acid or
oleum or, less commonly,
Nordhausen acid, is formed. Concentrations of oleum are either expressed in terms of% SO3 (called% oleum) or as% H2SO4 (the amount made if H2O were added); common concentrations are 40% oleum (109% H2SO4) and 65% oleum (114.6% H2SO4). Pure H2S2O7 is a solid with melting point 36°C.
Polarity and conductivity
Anhydrous H2SO4 is a very Chemical polarity liquid, having a
dielectric constant of around 100. This is because it can dissociate by
protonation itself, a process known as
autoprotolysis.Greenwood, N.N. and A. Earnshaw.
Chemistry of the Elements, pp 837-845. Pergamon Press, Oxford, UK, 1984. ISBN. It occurs to a high degree in sulfuric acid, more than 10 billion times the level seen in Water (molecule):
2 H2SO4 H3SO4+ + HSO4−
This allows protons to be highly mobile in H2SO4. It also makes sulfuric acid an excellent solvent for many reactions. In fact, the chemical equilibrium is more complex than shown above. 100% H2SO4 contains the following species at equilibrium (figures shown as mol per kg solvent): HSO4− (15.0), H3SO4+ (11.3), H3O+ (8.0), HS2O7− (4.4),
Oleum (3.6), H2O (0.1).
Chemical properties
Reaction with water
The
hydration reaction of sulfuric acid is highly exothermic reaction. If
water is added to the concentrated sulfuric acid, it can boil and spit dangerously. One should always add the acid to the water rather than the water to the acid. This can be remembered through
mnemonics such as: "Always do things as you oughta, add the acid to the water. If you think your life's too placid, add the water to the acid", "A.A.: Add Acid", or "Drop acid, not water", or "Acid to water, like
A&W Root Beer" or "Put the king into the water, not the water into the king" . The necessity for this safety precaution is due to the relative densities of these two liquids. Water is less
density than sulfuric acid, meaning water will tend to float on top of this acid. The reaction is best thought of as forming
hydronium ions, by
H2SO4 + H2O → H3O+ + HSO4−,
and then
HSO4- + H2O → H3O+ + SO42−.
Because the hydration of sulfuric acid is thermodynamically favorable, sulfuric acid is an excellent dehydrating agent, and is used to prepare many dried fruits. The affinity of sulfuric acid for water (molecule) is sufficiently strong that it will remove
hydrogen and oxygen atoms from other compounds; for example, mixing starch (C6H12O6)n and concentrated sulfuric acid will give elemental
carbon and water which is absorbed by the sulfuric acid (which becomes slightly diluted): (C6H12O6)n → 6C + 6H2O. The effect of this can be seen when concentrated sulfuric acid is spilled on paper; the starch reacts to give a
combustion appearance, the
carbon appears much as soot would in a fire. A more dramatic reaction occurs when sulfuric acid is added to a tablespoon of white sugar; a rigid column of black, porous carbon will quickly emerge. The carbon will smell strongly of caramel.
Other reactions of sulfuric acid
As an acid, sulfuric acid reacts with most base (chemistry) to give the corresponding
sulfate. For example,
copper(II) sulfate. This blue salt of
copper, commonly used for electroplating and as a fungicide, is prepared by the reaction of
copper(II) oxide with sulfuric acid:
Copper(II) oxide + H2SO4 →
Copper(II) sulfate +
Water (molecule)
Sulfuric acid can also be used to displace weaker acids from their salts. Reaction with sodium acetate, for example, displaces acetic acid:
H2SO4 +
Sodium acetate → Sodium bisulfate + Acetic acid
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 NO2+, 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.
Sulfuric acid reacts with most metals via a single displacement reaction to produce hydrogen gas and the metal sulfate. Dilute H2SO4 attacks iron,
aluminium, zinc, manganese,
magnesium and
nickel, but reactions with tin and copper require the acid to be hot and concentrated. Lead and tungsten, however, are resistant to sulfuric acid. The reaction with iron (shown) is typical for most of these metals, but the reaction with tin is unusual in that it produces sulfur dioxide rather than hydrogen.
Iron(s) + H2SO4(aq) →
Hydrogen(g) +
Iron(II) sulfate(aq)
Tin(s) + 2 H2SO4(aq) → Tin(II) sulfate(aq) + 2 H2O(l) + Sulfur dioxide(g)
Environmental aspects
Sulfuric acid is a constituent of acid rain, which is formed by atmospheric Redox of sulfur dioxide in the presence of water (molecule) - i.e. oxidation of sulfurous acid. Sulfur dioxide is the main byproduct produced when sulfur-containing fuels such as coal or oil are burned.
Sulfuric acid is formed naturally by the oxidation of sulphide minerals, such as iron sulfide. The resulting water can be highly acidic and is called
Acid mine drainage (ARD). This acidic water is capable of dissolving metals present in sulfide ores, which results in brightly-colored, toxic streams. The oxidation of iron sulfide pyrite by molecular oxygen produces iron(II), or Fe2+:
Pyrite + 7/2
oxygen + water → Fe2+ + 2
Sulfate + 2 Hydrogen ion.
The Fe2+ can be further oxidized to Fe3+, according to:
Fe2+ + 1/4 oxygen +
Hydrogen ion → Fe3+ + 1/2 water,
and the Fe3+ produced can be precipitated as the hydroxide or
hydrous oxide. The equation for the formation of the hydroxide is
Fe3+ + 3 water → Fe(OH)3 + 3
Hydrogen ion.
The iron(III) ion ("ferric iron", in casual nomenclature) can also oxidize pyrite. 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 Neutralization 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 form the dissolution of minerals from the acid-neutralization reaction with the minerals.
Extraterrestrial sulfuric acid
Sulfuric acid is produced in the upper atmosphere of Venus by the sun's
photochemistry action on
carbon dioxide, sulfur dioxide, and
water vapor.
Ultraviolet photons of wavelengths less than 169
nanometer can photodissociate
carbon dioxide into carbon monoxide and atomic oxygen. Atomic oxygen is highly reactive. When it reacts with sulfur dioxide, a trace component of the Venerian atmosphere, the result is
sulfur trioxide, which can combine with water vapor, another trace component of Venus' atmosphere, to yield sulfuric acid.
carbon dioxide →
carbon monoxide +
oxygen
sulfur dioxide +
oxygen →
sulfur trioxide
sulfur trioxide +
water → H2SO4
In the upper, cooler portions of Venus's atmosphere, sulfuric acid exists as a liquid, and thick sulfuric acid clouds completely obscure the planet's surface when viewed from above. The main cloud layer extends from 45–70
kilometer above the planet's surface, with thinner hazes extending as low as 30 and as high as 90 km above the surface.
Infrared spectra from NASA's Galileo mission show distinct absorptions on Jupiter's moon Europa (moon) that have been attributed to one or more sulfuric acid hydrates. The interpretation of the spectra is somewhat controversial. Some planetary scientists prefer to assign the spectral features to the sulfate ion, perhaps as part of one or more minerals on Europa's surface.
History of sulfuric acid
's 1808 sulfuric acid molecule shown a central sulfur atom bonded to three oxygen atoms.The discovery of sulfuric acid is credited to the 8th century Alchemy (Islam), Geber (Geber). The acid was later studied by 9th century Islamic medicine and alchemist
Al-Razi (Rhazes), who obtained the substance by dry distillation of minerals including iron(II) sulfate heptahydrate, FeSO4 • 7H2O, and copper(II) sulfate pentahydrate, CuSO4 • 5H2O. When heated, these compounds decompose to
iron(II) oxide and
copper(II) oxide, respectively, giving off
water (molecule) and
sulfur trioxide, which combine to produce a dilute solution of sulfuric acid. This method was popularized in Europe through translations of Arabic and Persian treatises, as well as books by European alchemists, such as the 13th-century German
Albertus Magnus.
Sulfuric acid was known to medieval European alchemists as
oil of vitriol,
spirit of vitriol, or simply
vitriol, among other names. The word vitriol derives from the Latin vitreus, 'glass', referring to the glassy appearance of the sulfate salts, which also carried the name vitriol. Salts called by this name included copper(II) sulfate (blue vitriol, or rarely Rome vitriol),
zinc sulfate (white vitriol), iron(II) sulfate (green vitriol), iron(III) sulfate (vitriol of Mars), and
cobalt(II) sulfate (red vitriol).
Vitriol was widely considered the most important alchemy substance, intended to be used as a
philosopher's stone. Highly purified vitriol was used as a medium for reacting other substances. This was largely because the acid does not react with gold, production of which was often the final goal of alchemical processes. The importance of vitriol to alchemy is highlighted in the alchemical motto,
Visita Interiora Terrae Rectificando Invenies Occultum Lapidem which is a backronym meaning ('Visit the interior of the earth and rectifying (i.e. purifying) you will find the hidden/secret stone'), found in
L'Azoth des Philosophes by the 15th Century alchemist Basilius Valentinus, .
In the 17th century, the German-Dutch chemist
Johann Glauber prepared sulfuric acid by burning
sulfur together with
Potassium nitrate (potassium nitrate, KNO3), in the presence of steam. As saltpeter decomposes, it oxidizes the sulfur to SO3, 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
lead chamber process allowed the effective industrialization of sulfuric acid production. After several refinements, this method remained the standard for sulfuric acid production for almost two centuries.
Sulfuric acid created by John Roebuck's process only approached a 35–40% concentration. Later refinements to the lead-chamber process by French chemist
Joseph-Louis Gay-Lussac and British chemist John Glover improved the yield 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 distillation minerals in a technique similar to the original alchemy processes. Pyrite (
iron disulfide, FeS2) was heated in air to yield iron (II) sulfate, FeSO4, 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.
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.
Uses
Sulfuric acid is a very important commodity chemical, and indeed, a nation's sulfuric acid production is a good indicator of its industrial strength.Chenier, Philip J.
Survey of Industrial Chemistry, pp 45-57. John Wiley & Sons, New York, 1987. ISBN. The major use (60% of total production worldwide) for sulfuric acid is in the "wet method" for the production of
phosphoric acid, used for manufacture of
phosphate fertilizers as well as
trisodium phosphate for detergents. 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:
fluorapatite + 5 H2SO4 + 10 water (molecule) → 5
calcium sulfate•2 H2O + hydrogen fluoride + 3
phosphoric acid.
Sulfuric acid is used in large quantities by the iron and
steelmaking industry to remove oxidation, rust and scale from rolled sheet and billets prior to sale to the
automobile and white-goods 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 (SO2) and sulfur trioxide (SO3) 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.
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 aluminum sulfate, also known as paper maker's alum. This can react with small amounts of soap on paper pulp fibers to give gelatinous aluminum carboxylates, which help to coagulate the pulp fibers into a hard paper surface. It is also used for making
aluminum hydroxide, which is used at
water treatment plants to
filter (water) out impurities, as well as to improve the taste of the
water. Aluminum sulfate is made by reacting bauxite with sulfuric acid:
aluminum oxide + 3 H2SO4 →
aluminum sulfate + 3
water (molecule).
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 cyclohexanoneoxime to caprolactam, used for making
nylon. It is used for making hydrochloric acid from salt via the
Mannheim process. Much H2SO4 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 important in the manufacture of
dyestuffs solutions and is the "acid" in lead-acid (car) batteries.
Sulfuric acid is also used as a general dehydrating agent in its concentrated form. See
sulfuric acid#Reaction with water.
Sulfur-iodine cycle
The
sulfur-iodine cycle is a series of thermo-chemical processes used to obtain
hydrogen. It consists of three chemical reactions whose net reactant is
water and whose net products are hydrogen and oxygen.
{|
|-| 2 → 2 + 2 + || || (830°C)|-| + + 2 → 2 + || || (120°C)|-| 2 → + || || (320°C)|}
The sulfur and
iodine compounds 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 economy. It does not require hydrocarbons like current methods of steam reforming.
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 large-scale.
Safety
Laboratory hazards
The corrosive properties of sulfuric acid are accentuated by its highly exothermic reaction with
water (molecule). Hence burns from sulfuric acid are potentially more serious than those of comparable strong acids (e.g. hydrochloric acid), as there is additional tissue damage due to dehydration and particularly due to the heat liberated by the reaction with water; i.e. secondary thermal damage. The danger is obviously greater with more concentrated preparations of sulfuric acid, but it should be remembered that even the normal laboratory "dilute" grade (approx. 1 M, 10%) will char paper by dehydration if left in contact for a sufficient while. Solutions equal to or stronger than 1.5 M should be labeled CORROSIVE, while solutions greater than 0.5 M but less than 1.5 M should be labeled IRRITANT. Fuming sulfuric acid (oleum) is not recommended for use in schools due to it being quite hazardous. The standard first aid treatment for acid spills on the skin is, as for other
corrosion agents, irrigation with large quantities of water: Washing should be continued for at least ten to fifteen minutes in order to cool the tissue surrounding the acid burn and to prevent secondary damage. Contaminated clothing must be removed immediately and the underlying skin washed thoroughly.
Preparation of the diluted acid can also be dangerous due to the heat released in the dilution process. It is essential that the concentrated acid is added to water and not the other way round, to take advantage of the relatively high heat capacity of water. Addition of water to concentrated sulfuric acid leads at best to the dispersal of a sulfuric acid
particulate, at worst to an
explosion. Preparation of solutions greater than 6 M (35%) in concentration is the most dangerous, as the heat produced can be sufficient to boil the diluted acid: efficient mechanical stirring and external cooling (e.g. an ice bath) are essential.
Industrial hazards
Although sulfuric acid is non-flammable, contact with metals in the event of a spillage can lead to the liberation of hydrogen gas. The dispersal of acid aerosols and gaseous sulfur dioxide is an additional hazard of fires involving sulfuric acid.
Sulfuric acid is not considered toxic besides its obvious corrosive hazard, and the main occupational risks 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. In the United States, the
permissible exposure limit (PEL) for sulfuric acid is fixed at 1 mg/m³: limits in other countries are similar. Interestingly 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,
Societal and cultural aspects
Metaphorical usage
Vitriol may be used metaphorically, as in a diatribe or verbal upbraiding.
In fiction
The use of sulfuric acid as a weapon in crimes of assault, known as "
Vitriolage", has at times been sufficiently common (if sensational) to make its way into novels and short stories. Examples include
The Adventure of the Illustrious Client, by
Arthur Conan Doyle,
The Love of Long Ago, by
Guy de Maupassant and
Brighton Rock (novel) by Graham Greene. A band, My Vitriol, take their name from its use as a weapon in
Brighton Rock. An episode of
Saturday Night Live hosted by
Mel Gibson included a parody Western sketch about "Sheriff Jeff Acid," who carries a flask of acid instead of a six shooter. The DC Comics villain
Two Face was disfigured as a result of a vitriol throw. This crime is also mentioned in
Nineteen Eighty-Four by George Orwell; the protagonist Winston Smith agrees to throw vitriol into a child's face if that would be "the Brotherhood's" order, and Winston's enemy O'Brien later uses those barbaric words to undermine his logic. The novel
Veronika Decides to Die by
Paulo Coelho talks of a girl who has attempted to commit suicide and ends up with vitriol poisoning. The doctor/therapist in this novel also writes a thesis on curing vitriol poisoning. The substance was also used by a young gangster in Season 6B, Episode 5 of
The Sopranos as a form of torture.
In comic rhyme
Sulfuric acid is one of the few compounds whose chemical formula is well known by the general public because of many comic rhymes, such as this one:
Billy was a chemist, but Billy is no more,
What Billy thought was H2O was H2SO4.
A common variant is this:
Little Lucy in the lab, dead upon the floor,
For what she thought was H2O was H2SO4.
Legal controls and regulation
International commerce of sulfuric acid is controlled under the
United Nations Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances, 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. Annex to Form D ("Red List"), 11th Edition, January 2007 (pg. 4).
International Narcotics Control Board.
Vienna, Austria; 2007.
In the United States of America, sulfuric acid is included in
DEA list of chemicals#List II chemicals of the
DEA list of chemicals established pursuant to the
Chemical Diversion and Trafficking Act. Accordingly, transactions of sulfuric acid—such as sales, transfers, exports from and imports to the United States—are subject to regulation and monitoring by the Drug Enforcement Administration. 66 FR 52670—52675. 17 October 2001. 21 CFR 1309 21 USC, Chapter 13 (Controlled Substances Act)
References
- Institut National de Recherche et de Sécurité. (1997). "Acide sulfurique". Fiche toxicologique n°30, Paris: INRS, 5 pp.
- Handbook of Chemistry and Physics, 71st edition, CRC Press, Ann Arbor, Michigan, 1990.
- Agamanolis DP. Metabolic and toxic disorders. In: Prayson R, editor. Neuropathology: a volume in the foundations in diagnostic pathology series. Philadelphia: Elsevier/Churchill Livingstone, 2005; 413-315.
External links
-
- NIOSH Pocket Guide to Chemical Hazards
- External Material Safety Data Sheet
- Sulfuric acid analysis - titration freeware
{{Chembox new| Name = Sulfuric acid| ImageFile = Sulfuric-acid-2D-dimensions.svg| ImageFile1 = Sulfuric-acid-3D-vdW.png| IUPACName = Sulfuric Acid| OtherNames = oil of vitriol| Section1 = {{Chembox Identifiers| CASNo = 7664-93-9| RTECS = WS5600000 -->
| Section2 = {{Chembox Properties| Formula = H2SO4 (aq)| MolarMass = 98.07848 g mol−1| Appearance = clear, colorless,odorless liquid| Density = 1.84 g cm−3, liquid| Solubility = fully miscible
(exothermic)| MeltingPt = 10 °C (283 K)| BoilingPt = 338 °C (611 K)| Viscosity = 26.7 cPoise at 20°C -->
| Section7 = {{Chembox Hazards| FlashPt = Non-flammable| EUClass = Corrosive (
C)| NFPA-H = 3| NFPA-F = 0| NFPA-R = 2| NFPA-O = COR| RPhrases = | SPhrases = , , , -->
| Section8 = {{Chembox Related| Function =
strong acids]
Hydrochloric acidNitric acid
[Sulfurous acid
Peroxymonosulfuric acidSulfur trioxideOleum-->-->
Sulfuric (or sulphuric) acid, hydrogen2
sulfuroxygen4, is a strong
mineral acid. It is soluble in
water at all concentrations. It was once known as
oil of vitriol, coined by the 8th-century Alchemy (Islam) Geber (Geber) after his discovery of the chemical.Khairallah, Amin A.
Outline of Arabic Contributions to Medicine, chapter 10. Beirut, 1946. Sulfuric acid has many applications, and is one of the top products of the
chemical industry. World production in 2001 was 165 million tonnes, with an approximate value of US$8 billion. Principal uses include
ore processing, fertilizer manufacturing,
Oil refinery,
wastewater processing, and chemical synthesis.
Many proteins are made of
sulfur-containing amino
acids (such as
cysteine and
methionine) which produce sulfuric acid when
metabolism by the body.
Manufacture
Sulfuric acid is produced from
sulfur, oxygen and water via the
contact process.
In the first step,
sulfur is burned to produce
sulfur dioxide.
(1) (
Solid) + Oxygen(Gas) →
Sulfur dioxide(g)
This is then oxidised to
sulfur trioxide using
oxygen in the presence of a vanadium(V) oxide
catalyst.
(2) 2 SO2 + O2(g) →
Sulfur trioxide(g) (in presence of Vanadium pentoxide)
Finally the sulfur trioxide is treated with water (usually as 97-98% H2SO4 containing 2-3% water) to produce 98-99% sulfuric acid.
(3) SO3(g) + Water (molecule)(
liquid) → H2SO4(l)
Note that directly dissolving SO3 in water is impractical due to the highly exothermic nature of the reaction. Mists are formed instead of a liquid.Alternatively, SO3 can be absorbed into H2SO4 to produce oleum (H2S2O7), which may then be mixed with water to form sulfuric acid.
(3) H2SO4
(liquid) + SO3 → H2S2O7
(l)
Oleum is reacted with water to form concentrated H2SO4.
(4) H2S2O7
(l) + H2O
(l) → 2 H2SO4
(l)
In 1993, American production of sulfuric acid amounted to 36.4 million tonnes. World production in 2001 was 165 million tonnes.
Physical properties
Forms of sulfuric acid
Although nearly 100% sulfuric acid can be made, this loses sulfur trioxide at the boiling point to produce 98.3% acid. The 98% 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
- 10%, dilute sulfuric acid for laboratory use,
- 33.5%, battery acid (used in lead-acid battery),
- 62.18%, chamber or fertilizer acid,
- 77.67%, tower or Glover acid,
- 98%, concentrated acid.
Different purities are also available. Technical grade H2SO4 is impure and often colored, but is suitable for making fertilizer. Pure grades such as US
Pharmacopoeia (USP) grade are used for making pharmaceuticals and
dyestuffs.
When high concentrations of SO3
(gas) are added to sulfuric acid, H2S2O7, called
pyrosulfuric acid,
fuming sulfuric acid or
oleum or, less commonly,
Nordhausen acid, is formed. Concentrations of oleum are either expressed in terms of% SO3 (called% oleum) or as% H2SO4 (the amount made if H2O were added); common concentrations are 40% oleum (109% H2SO4) and 65% oleum (114.6% H2SO4). Pure H2S2O7 is a solid with melting point 36°C.
Polarity and conductivity
Anhydrous H2SO4 is a very
Chemical polarity liquid, having a dielectric constant of around 100. This is because it can dissociate by protonation itself, a process known as autoprotolysis.Greenwood, N.N. and A. Earnshaw.
Chemistry of the Elements, pp 837-845. Pergamon Press, Oxford, UK, 1984. ISBN. It occurs to a high degree in sulfuric acid, more than 10 billion times the level seen in Water (molecule):
2 H2SO4 H3SO4+ + HSO4−
This allows protons to be highly mobile in H2SO4. It also makes sulfuric acid an excellent solvent for many reactions. In fact, the chemical equilibrium is more complex than shown above. 100% H2SO4 contains the following species at equilibrium (figures shown as mol per kg solvent): HSO4− (15.0), H3SO4+ (11.3), H3O+ (8.0), HS2O7− (4.4), Oleum (3.6), H2O (0.1).
Chemical properties
Reaction with water
The hydration reaction of sulfuric acid is highly exothermic reaction. If
water is added to the concentrated sulfuric acid, it can boil and spit dangerously. One should always add the acid to the water rather than the water to the acid. This can be remembered through mnemonics such as: "Always do things as you oughta, add the acid to the water. If you think your life's too placid, add the water to the acid", "A.A.: Add Acid", or "Drop acid, not water", or "Acid to water, like A&W Root Beer" or "Put the king into the water, not the water into the king" . The necessity for this safety precaution is due to the relative densities of these two liquids. Water is less density than sulfuric acid, meaning water will tend to float on top of this acid. The reaction is best thought of as forming hydronium ions, by
H2SO4 + H2O → H3O+ + HSO4−,
and then
HSO4- + H2O → H3O+ + SO42−.
Because the hydration of sulfuric acid is
thermodynamically favorable, sulfuric acid is an excellent dehydrating agent, and is used to prepare many dried fruits. The affinity of sulfuric acid for
water (molecule) is sufficiently strong that it will remove hydrogen and
oxygen atoms from other compounds; for example, mixing starch (C6H12O6)n and concentrated sulfuric acid will give elemental
carbon and water which is absorbed by the sulfuric acid (which becomes slightly diluted): (C6H12O6)n → 6C + 6H2O. The effect of this can be seen when concentrated sulfuric acid is spilled on paper; the starch reacts to give a
combustion appearance, the carbon appears much as soot would in a fire. A more dramatic reaction occurs when sulfuric acid is added to a tablespoon of white sugar; a rigid column of black, porous carbon will quickly emerge. The carbon will smell strongly of caramel.
Other reactions of sulfuric acid
As an acid, sulfuric acid reacts with most
base (chemistry) to give the corresponding sulfate. For example, copper(II) sulfate. This blue salt of
copper, commonly used for
electroplating and as a fungicide, is prepared by the reaction of copper(II) oxide with sulfuric acid:
Copper(II) oxide + H2SO4 →
Copper(II) sulfate +
Water (molecule)
Sulfuric acid can also be used to displace weaker acids from their salts. Reaction with
sodium acetate, for example, displaces
acetic acid:
H2SO4 +
Sodium acetate → Sodium bisulfate + Acetic acid
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 NO2+, 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.
Sulfuric acid reacts with most metals via a single displacement reaction to produce
hydrogen gas and the metal sulfate. Dilute H2SO4 attacks
iron,
aluminium,
zinc, manganese, magnesium and
nickel, but reactions with tin and
copper require the acid to be hot and concentrated.
Lead and
tungsten, however, are resistant to sulfuric acid. The reaction with iron (shown) is typical for most of these metals, but the reaction with tin is unusual in that it produces sulfur dioxide rather than hydrogen.
Iron(s) + H2SO4(aq) → Hydrogen(g) + Iron(II) sulfate(aq)
Tin(s) + 2 H2SO4(aq) → Tin(II) sulfate(aq) + 2 H2O(l) +
Sulfur dioxide(g)
Environmental aspects
Sulfuric acid is a constituent of acid rain, which is formed by atmospheric Redox of sulfur dioxide in the presence of
water (molecule) - i.e. oxidation of sulfurous acid. Sulfur dioxide is the main byproduct produced when sulfur-containing fuels such as coal or oil are burned.
Sulfuric acid is formed naturally by the oxidation of sulphide minerals, such as iron sulfide. The resulting water can be highly acidic and is called Acid mine drainage (ARD). This acidic water is capable of dissolving metals present in sulfide ores, which results in brightly-colored, toxic streams. The oxidation of iron sulfide pyrite by molecular oxygen produces iron(II), or Fe2+:
Pyrite + 7/2 oxygen +
water → Fe2+ + 2 Sulfate + 2
Hydrogen ion.
The Fe2+ can be further oxidized to Fe3+, according to:
Fe2+ + 1/4 oxygen +
Hydrogen ion → Fe3+ + 1/2
water,
and the Fe3+ produced can be precipitated as the
hydroxide or hydrous oxide. The equation for the formation of the hydroxide is
Fe3+ + 3
water → Fe(OH)3 + 3 Hydrogen ion.
The iron(III) ion ("ferric iron", in casual nomenclature) can also oxidize pyrite. 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 Neutralization 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 form the dissolution of minerals from the acid-neutralization reaction with the minerals.
Extraterrestrial sulfuric acid
Sulfuric acid is produced in the upper atmosphere of Venus by the sun's photochemistry action on
carbon dioxide,
sulfur dioxide, and water vapor. Ultraviolet
photons of wavelengths less than 169
nanometer can photodissociate carbon dioxide into
carbon monoxide and atomic oxygen. Atomic oxygen is highly reactive. When it reacts with sulfur dioxide, a trace component of the Venerian atmosphere, the result is sulfur trioxide, which can combine with water vapor, another trace component of Venus' atmosphere, to yield sulfuric acid.
carbon dioxide →
carbon monoxide +
oxygen
sulfur dioxide + oxygen → sulfur trioxide
sulfur trioxide +
water → H2SO4
In the upper, cooler portions of Venus's atmosphere, sulfuric acid exists as a liquid, and thick sulfuric acid clouds completely obscure the planet's surface when viewed from above. The main cloud layer extends from 45–70 kilometer above the planet's surface, with thinner hazes extending as low as 30 and as high as 90 km above the surface.
Infrared spectra from NASA's Galileo mission show distinct absorptions on
Jupiter's moon Europa (moon) that have been attributed to one or more sulfuric acid hydrates. The interpretation of the spectra is somewhat controversial. Some planetary scientists prefer to assign the spectral features to the sulfate ion, perhaps as part of one or more minerals on Europa's surface.
History of sulfuric acid
's 1808 sulfuric acid molecule shown a central sulfur atom bonded to three oxygen atoms.The discovery of sulfuric acid is credited to the 8th century
Alchemy (Islam),
Geber (Geber). The acid was later studied by 9th century
Islamic medicine and alchemist Al-Razi (Rhazes), who obtained the substance by dry distillation of minerals including
iron(II) sulfate heptahydrate, FeSO4 • 7H2O, and
copper(II) sulfate pentahydrate, CuSO4 • 5H2O. When heated, these compounds decompose to iron(II) oxide and copper(II) oxide, respectively, giving off water (molecule) and sulfur trioxide, which combine to produce a dilute solution of sulfuric acid. This method was popularized in Europe through translations of Arabic and Persian treatises, as well as books by European alchemists, such as the 13th-century German Albertus Magnus.
Sulfuric acid was known to medieval European alchemists as
oil of vitriol,
spirit of vitriol, or simply
vitriol, among other names. The word vitriol derives from the Latin vitreus, 'glass', referring to the glassy appearance of the sulfate salts, which also carried the name vitriol. Salts called by this name included
copper(II) sulfate (blue vitriol, or rarely Rome vitriol), zinc sulfate (white vitriol),
iron(II) sulfate (green vitriol), iron(III) sulfate (vitriol of Mars), and cobalt(II) sulfate (red vitriol).
Vitriol was widely considered the most important alchemy substance, intended to be used as a philosopher's stone. Highly purified vitriol was used as a medium for reacting other substances. This was largely because the acid does not react with
gold, production of which was often the final goal of alchemical processes. The importance of vitriol to alchemy is highlighted in the alchemical motto,
Visita Interiora Terrae Rectificando Invenies Occultum Lapidem which is a
backronym meaning ('Visit the interior of the earth and rectifying (i.e. purifying) you will find the hidden/secret stone'), found in
L'Azoth des Philosophes by the 15th Century alchemist
Basilius Valentinus, .
In the 17th century, the German-Dutch chemist Johann Glauber prepared sulfuric acid by burning
sulfur together with Potassium nitrate (
potassium nitrate, KNO3), in the presence of steam. As saltpeter decomposes, it oxidizes the sulfur to SO3, 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
lead chamber process allowed the effective industrialization of sulfuric acid production. After several refinements, this method remained the standard for sulfuric acid production for almost two centuries.
Sulfuric acid created by John Roebuck's process only approached a 35–40% concentration. Later refinements to the lead-chamber process by French chemist Joseph-Louis Gay-Lussac and British chemist John Glover improved the yield 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 distillation minerals in a technique similar to the original
alchemy processes. Pyrite (iron disulfide, FeS2) was heated in air to yield iron (II) sulfate, FeSO4, 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.
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.
Uses
Sulfuric acid is a very important
commodity chemical, and indeed, a nation's sulfuric acid production is a good indicator of its industrial strength.Chenier, Philip J.
Survey of Industrial Chemistry, pp 45-57. John Wiley & Sons, New York, 1987. ISBN. The major use (60% of total production worldwide) for sulfuric acid is in the "wet method" for the production of
phosphoric acid, used for manufacture of
phosphate fertilizers as well as trisodium phosphate for detergents. 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:
fluorapatite + 5 H2SO4 + 10 water (molecule) → 5
calcium sulfate•2 H2O +
hydrogen fluoride + 3 phosphoric acid.
Sulfuric acid is used in large quantities by the iron and
steelmaking industry to remove oxidation, rust and scale from rolled sheet and billets prior to sale to the
automobile and white-goods 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 (SO2) and sulfur trioxide (SO3) 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.
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 aluminum sulfate, also known as paper maker's alum. This can react with small amounts of soap on paper pulp fibers to give gelatinous aluminum
carboxylates, which help to coagulate the pulp fibers into a hard paper surface. It is also used for making
aluminum hydroxide, which is used at
water treatment plants to filter (water) out impurities, as well as to improve the taste of the
water. Aluminum sulfate is made by reacting
bauxite with sulfuric acid:
aluminum oxide + 3 H2SO4 →
aluminum sulfate + 3 water (molecule).
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
cyclohexanoneoxime to
caprolactam, used for making
nylon. It is used for making hydrochloric acid from salt via the Mannheim process. Much H2SO4 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 important in the manufacture of
dyestuffs solutions and is the "acid" in lead-acid (car) batteries.
Sulfuric acid is also used as a general dehydrating agent in its concentrated form. See sulfuric acid#Reaction with water.
Sulfur-iodine cycle
The sulfur-iodine cycle is a series of thermo-chemical processes used to obtain
hydrogen. It consists of three chemical reactions whose net reactant is water and whose net products are hydrogen and
oxygen.
{|
|-| 2 → 2 + 2 + || || (830°C)|-| + + 2 → 2 + || || (120°C)|-| 2 → + || || (320°C)|}
The sulfur and iodine compounds 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 economy. It does not require
hydrocarbons like current methods of steam reforming.
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 large-scale.
Safety
Laboratory hazards
The corrosive properties of sulfuric acid are accentuated by its highly
exothermic reaction with water (molecule). Hence burns from sulfuric acid are potentially more serious than those of comparable strong acids (e.g.
hydrochloric acid), as there is additional tissue damage due to dehydration and particularly due to the heat liberated by the reaction with water; i.e. secondary thermal damage. The danger is obviously greater with more concentrated preparations of sulfuric acid, but it should be remembered that even the normal laboratory "dilute" grade (approx. 1 M, 10%) will char paper by dehydration if left in contact for a sufficient while. Solutions equal to or stronger than 1.5 M should be labeled CORROSIVE, while solutions greater than 0.5 M but less than 1.5 M should be labeled IRRITANT. Fuming sulfuric acid (oleum) is not recommended for use in schools due to it being quite hazardous. The standard first aid treatment for acid spills on the skin is, as for other corrosion agents, irrigation with large quantities of water: Washing should be continued for at least ten to fifteen minutes in order to cool the tissue surrounding the acid burn and to prevent secondary damage. Contaminated clothing must be removed immediately and the underlying skin washed thoroughly.
Preparation of the diluted acid can also be dangerous due to the heat released in the dilution process. It is essential that the concentrated acid is added to water and not the other way round, to take advantage of the relatively high heat capacity of water. Addition of water to concentrated sulfuric acid leads at best to the dispersal of a sulfuric acid
particulate, at worst to an
explosion. Preparation of solutions greater than 6 M (35%) in concentration is the most dangerous, as the heat produced can be sufficient to boil the diluted acid: efficient mechanical stirring and external cooling (e.g. an ice bath) are essential.
Industrial hazards
Although sulfuric acid is non-flammable, contact with metals in the event of a spillage can lead to the liberation of
hydrogen gas. The dispersal of acid aerosols and gaseous sulfur dioxide is an additional hazard of fires involving sulfuric acid.
Sulfuric acid is not considered toxic besides its obvious corrosive hazard, and the main occupational risks 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. In the
United States, the
permissible exposure limit (PEL) for sulfuric acid is fixed at 1 mg/m³: limits in other countries are similar. Interestingly 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,
Societal and cultural aspects
Metaphorical usage
Vitriol may be used metaphorically, as in a diatribe or verbal upbraiding.
In fiction
The use of sulfuric acid as a weapon in crimes of assault, known as "Vitriolage", has at times been sufficiently common (if sensational) to make its way into novels and short stories. Examples include The Adventure of the Illustrious Client, by Arthur Conan Doyle, The Love of Long Ago, by
Guy de Maupassant and
Brighton Rock (novel) by
Graham Greene. A band,
My Vitriol, take their name from its use as a weapon in
Brighton Rock. An episode of
Saturday Night Live hosted by
Mel Gibson included a parody Western sketch about "Sheriff Jeff Acid," who carries a flask of acid instead of a six shooter. The
DC Comics villain
Two Face was disfigured as a result of a vitriol throw. This crime is also mentioned in
Nineteen Eighty-Four by
George Orwell; the protagonist Winston Smith agrees to throw vitriol into a child's face if that would be "the Brotherhood's" order, and Winston's enemy O'Brien later uses those barbaric words to undermine his logic. The novel
Veronika Decides to Die by Paulo Coelho talks of a girl who has attempted to commit suicide and ends up with vitriol poisoning. The doctor/therapist in this novel also writes a thesis on curing vitriol poisoning. The substance was also used by a young gangster in Season 6B, Episode 5 of The Sopranos as a form of torture.
In comic rhyme
Sulfuric acid is one of the few compounds whose chemical formula is well known by the general public because of many comic
rhymes, such as this one:
Billy was a chemist, but Billy is no more,
What Billy thought was H2O was H2SO4.
A common variant is this:
Little Lucy in the lab, dead upon the floor,
For what she thought was H2O was H2SO4.
Legal controls and regulation
International commerce of sulfuric acid is controlled under the
United Nations Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances, 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. Annex to Form D ("Red List"), 11th Edition, January 2007 (pg. 4).
International Narcotics Control Board. Vienna, Austria; 2007.
In the
United States of America, sulfuric acid is included in
DEA list of chemicals#List II chemicals of the DEA list of chemicals established pursuant to the
Chemical Diversion and Trafficking Act. Accordingly, transactions of sulfuric acid—such as sales, transfers, exports from and imports to the United States—are subject to regulation and monitoring by the Drug Enforcement Administration. 66 FR 52670—52675. 17 October 2001. 21 CFR 1309 21 USC, Chapter 13 (Controlled Substances Act)
References
- Institut National de Recherche et de Sécurité. (1997). "Acide sulfurique". Fiche toxicologique n°30, Paris: INRS, 5 pp.
- Handbook of Chemistry and Physics, 71st edition, CRC Press, Ann Arbor, Michigan, 1990.
- Agamanolis DP. Metabolic and toxic disorders. In: Prayson R, editor. Neuropathology: a volume in the foundations in diagnostic pathology series. Philadelphia: Elsevier/Churchill Livingstone, 2005; 413-315.
External links
-
- NIOSH Pocket Guide to Chemical Hazards
- External Material Safety Data Sheet
- Sulfuric acid analysis - titration freeware
Sulfuric acid - Wikipedia, the free encyclopedia
Sulfuric acid (also spelled sulphuric acid) is a strong mineral acid with the molecular formula H 2 S O 4. It is soluble in water at all concentrations.
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Chemical Safety Data: Sulfuric acid ... Common synonyms: Sulphuric acid, vitriol, oil of vitriol: Formula: H 2 SO 4: Physical properties
SULFURIC ACID, 52 - 100 %
1. Product Identification Synonyms: Oil of vitriol; Babcock acid; sulphuric acid CAS No.: 7664-93-9 Molecular Weight: 98.08
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sulfuric acid /sul·fur·ic ac·id/ (sul-fur´ik) an oily, highly caustic, poisonous acid, H2SO4, widely used in chemistry, industry, and the arts.
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Physical Description Colorless to dark-brown, oily, odorless liquid. [Note: Pure compound is a solid below 51°F. Often used in an aqueous solution.]
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