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Wikipedia

Hydrogen peroxide

Hydrogen peroxide is a chemical compound with the formula H2O2. In its pure form, it is a very pale blue[5] liquid that is slightly more viscous than water. It is used as an oxidizer, bleaching agent, and antiseptic, usually as a dilute solution (3%–6% by weight) in water for consumer use, and in higher concentrations for industrial use. Concentrated hydrogen peroxide, or "high-test peroxide", decomposes explosively when heated and has been used as a propellant in rocketry.[6]

Hydrogen peroxide

Ball stick model of the hydrogen peroxide molecule
Names
IUPAC name
Hydrogen peroxide
Other names
Dioxidane
Oxidanyl
Perhydroxic acid
0-hydroxyol
Dihydrogen dioxide
Oxygenated water
Peroxaan
Identifiers
  • 7722-84-1 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:16240 Y
ChEMBL
  • ChEMBL71595 Y
ChemSpider
  • 763 Y
ECHA InfoCard 100.028.878
EC Number
  • 231-765-0
  • 2448
KEGG
  • D00008 Y
  • 784
RTECS number
  • MX0900000 (>90% soln.)
    MX0887000 (>30% soln.)
UNII
  • BBX060AN9V Y
UN number 2015 (>60% soln.)
2014 (20–60% soln.)
2984 (8–20% soln.)
  • DTXSID2020715
  • InChI=1S/H2O2/c1-2/h1-2H Y
    Key: MHAJPDPJQMAIIY-UHFFFAOYSA-N Y
  • InChI=1/H2O2/c1-2/h1-2H
    Key: MHAJPDPJQMAIIY-UHFFFAOYAL
  • OO
Properties
H2O2
Molar mass 34.0147 g/mol
Appearance Very light blue liquid
Odor slightly sharp
Density 1.11 g/cm3 (20 °C, 30% (w/w) solution)[1]
1.450 g/cm3 (20 °C, pure)
Melting point −0.43 °C (31.23 °F; 272.72 K)
Boiling point 150.2 °C (302.4 °F; 423.3 K) (decomposes)
Miscible
Solubility soluble in ether, alcohol
insoluble in petroleum ether
log P -0.43[2]
Vapor pressure 5 mmHg (30 °C)[3]
Acidity (pKa) 11.75
−17.7·10−6 cm3/mol
1.4061
Viscosity 1.245 cP (20 °C)
2.26 D
Thermochemistry
1.267 J/(g·K) (gas)
2.619 J/(g·K) (liquid)
−187.80 kJ/mol
Pharmacology
A01AB02 (WHO) D08AX01 (WHO), D11AX25 (WHO), S02AA06 (WHO)
Hazards
GHS labelling:
Danger
H271, H302, H314, H332, H335, H412
P280, P305+P351+P338, P310
NFPA 704 (fire diamond)
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
1518 mg/kg[citation needed]
2000 mg/kg (oral, mouse)[4]
1418 ppm (rat, 4 hr)[4]
227 ppm (mouse)[4]
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 1 ppm (1.4 mg/m3)[3]
REL (Recommended)
TWA 1 ppm (1.4 mg/m3)[3]
IDLH (Immediate danger)
75 ppm[3]
Safety data sheet (SDS) ICSC 0164 (>60% soln.)
Related compounds
Related compounds
Water
Ozone
Hydrazine
Hydrogen disulfide
Dioxygen difluoride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)

Hydrogen peroxide is a reactive oxygen species and the simplest peroxide, a compound having an oxygen–oxygen single bond. It decomposes slowly into water and elemental oxygen when exposed to light, and rapidly in the presence of organic or reactive compounds. It is typically stored with a stabilizer in a weakly acidic solution in a dark bottle to block light. Hydrogen peroxide is found in biological systems including the human body. Enzymes that use or decompose hydrogen peroxide are classified as peroxidases.

Properties

The boiling point of H2O2 has been extrapolated as being 150.2 °C (302.4 °F), approximately 50 °C (90 °F) higher than water. In practice, hydrogen peroxide will undergo potentially explosive thermal decomposition if heated to this temperature. It may be safely distilled at lower temperatures under reduced pressure.[7]

Structure

 
Structure and dimensions of H2O2 in the gas phase
 
Structure and dimensions of H2O2 in the solid (crystalline) phase

Hydrogen peroxide (H2O2) is a nonplanar molecule with (twisted) C2 symmetry; this was first shown by Paul-Antoine Giguère in 1950 using infrared spectroscopy.[8][9] Although the O−O bond is a single bond, the molecule has a relatively high rotational barrier of 386 cm−1 (4.62 kJ/mol) for rotation between enantiomers via the trans configuration, and 2460 cm−1 (29.4 kJ/mol) via the cis configuration.[10] These barriers are proposed to be due to repulsion between the lone pairs of the adjacent oxygen atoms and dipolar effects between the two O–H bonds. For comparison, the rotational barrier for ethane is 1040 cm−1 (12.4 kJ/mol).

The approximately 100° dihedral angle between the two O–H bonds makes the molecule chiral. It is the smallest and simplest molecule to exhibit enantiomerism. It has been proposed that the enantiospecific interactions of one rather than the other may have led to amplification of one enantiomeric form of ribonucleic acids and therefore an origin of homochirality in an RNA world.[11]

The molecular structures of gaseous and crystalline H2O2 are significantly different. This difference is attributed to the effects of hydrogen bonding, which is absent in the gaseous state.[12] Crystals of H2O2 are tetragonal with the space group D4
4
or P41212.[13]

Aqueous solutions

In aqueous solutions, hydrogen peroxide differs from the pure substance due to the effects of hydrogen bonding between water and hydrogen peroxide molecules. Hydrogen peroxide and water form a eutectic mixture, exhibiting freezing-point depression down as low as -56 °C; pure water has a freezing point of 0 °C and pure hydrogen peroxide of -0.43 °C. The boiling point of the same mixtures is also depressed in relation with the mean of both boiling points (125.1 °C). It occurs at 114 °C. This boiling point is 14 °C greater than that of pure water and 36.2 °C less than that of pure hydrogen peroxide.[14]

  •  
    Phase diagram of H2O2 and water: Area above blue line is liquid. Dotted lines separate solid–liquid phases from solid–solid phases.
  • Density of aqueous solution of H2O2
    H2O2 (w/w) Density
    (g/cm3)
    Temp.
    (°C)
    3% 1.0095 15
    27% 1.10 20
    35% 1.13 20
    50% 1.20 20
    70% 1.29 20
    75% 1.33 20
    96% 1.42 20
    98% 1.43 20
    100% 1.45 20
  • Comparison with analogues

    Hydrogen peroxide has several structural analogues with HmX−XHn bonding arrangements (water also shown for comparison). It has the highest (theoretical) boiling point of this series (X = O, S, N, P). Its melting point is also fairly high, being comparable to that of hydrazine and water, with only hydroxylamine crystallising significantly more readily, indicative of particularly strong hydrogen bonding. Diphosphane and hydrogen disulfide exhibit only weak hydrogen bonding and have little chemical similarity to hydrogen peroxide. Structurally, the analogues all adopt similar skewed structures, due to repulsion between adjacent lone pairs.

    Properties of H2O2 and its analogues
    Values marked * are extrapolated
    Name Formula Molar mass
    (g/mol)
    Melting
    point (°C)
    Boiling
    point (°C)
    Water HOH 18.02 0.00 99.98
    Hydrogen peroxide HOOH 34.01 −0.43 150.2*
    Hydrogen disulfide HSSH 66.15 −89.6 70.7
    Hydrazine H2NNH2 32.05 2 114
    Hydroxylamine NH2OH 33.03 33 58*
    Diphosphane H2PPH2 65.98 −99 63.5*

    Discovery

    Alexander von Humboldt is sometimes said to have been the first to report the first synthetic peroxide, barium peroxide, in 1799 as a by-product of his attempts to decompose air, although this is disputed due to von Humboldt's ambiguous wording.[15] Nineteen years later Louis Jacques Thénard recognized that this compound could be used for the preparation of a previously unknown compound, which he described as eau oxygénée ("oxygenated water") – subsequently known as hydrogen peroxide.[16][17][18] Today, the term "oxygenated water" may appear on retail packaging referring to mixtures containing either water and hydrogen peroxide or water and dissolved oxygen. This could cause personal injury if the difference is not properly understood by the user.[19]

    An improved version of Thénard's process used hydrochloric acid, followed by addition of sulfuric acid to precipitate the barium sulfate byproduct. This process was used from the end of the 19th century until the middle of the 20th century.[20]

    The bleaching effect of peroxides and their salts on natural dyes had been known since Thénard's experiments in the 1820s, but early attempts of industrial production of peroxides failed. The first plant producing hydrogen peroxide was built in 1873 in Berlin. The discovery of the synthesis of hydrogen peroxide by electrolysis with sulfuric acid introduced the more efficient electrochemical method. It was first commercialized in 1908 in Weißenstein, Carinthia, Austria. The anthraquinone process, which is still used, was developed during the 1930s by the German chemical manufacturer IG Farben in Ludwigshafen. The increased demand and improvements in the synthesis methods resulted in the rise of the annual production of hydrogen peroxide from 35,000 tonnes in 1950, to over 100,000 tonnes in 1960, to 300,000 tonnes by 1970; by 1998 it reached 2.7 million tonnes.[21]

    Early attempts failed to produce neat hydrogen peroxide. Anhydrous hydrogen peroxide was first obtained by vacuum distillation.[22]

    Determination of the molecular structure of hydrogen peroxide proved to be very difficult. In 1892, the Italian physical chemist Giacomo Carrara (1864–1925) determined its molecular mass by freezing-point depression, which confirmed that its molecular formula is H2O2.[23] H2O=O seemed to be just as possible as the modern structure, and as late as in the middle of the 20th century at least half a dozen hypothetical isomeric variants of two main options seemed to be consistent with the available evidence.[24] In 1934, the English mathematical physicist William Penney and the Scottish physicist Gordon Sutherland proposed a molecular structure for hydrogen peroxide that was very similar to the presently accepted one.[25][26]

    Previously, hydrogen peroxide was prepared industrially by hydrolysis of ammonium persulfate:

     

    which was itself obtained by the electrolysis of a solution of ammonium bisulfate ([NH4]HSO4) in sulfuric acid:[27]

     

    Production

     
    Catalytic cycle for the anthraquinone process to produce hydrogen peroxide: an anthraquinone (right) is reduced using hydrogen to produce the corresponding anthrahydroquinone (left). This is oxidized using oxygen to produce hydrogen peroxide and recover anthraquinone.

    Today, hydrogen peroxide is manufactured almost exclusively by the anthraquinone process, which was originally developed by BASF in 1939. It begins with the reduction of an anthraquinone (such as 2-ethylanthraquinone or the 2-amyl derivative) to the corresponding anthrahydroquinone, typically by hydrogenation on a palladium catalyst. In the presence of oxygen, the anthrahydroquinone then undergoes autoxidation: the labile hydrogen atoms of the hydroxy groups transfer to the oxygen molecule, to give hydrogen peroxide and regenerating the anthraquinone. Most commercial processes achieve oxidation by bubbling compressed air through a solution of the anthrahydroquinone, with the hydrogen peroxide then extracted from the solution and the anthraquinone recycled back for successive cycles of hydrogenation and oxidation.[28][29]

    The net reaction for the anthraquinone-catalyzed process is :[28]

    H2 + O2 → H2O2

    The economics of the process depend heavily on effective recycling of the extraction solvents, the hydrogenation catalyst and the expensive quinone.

     
    ISO tank container for hydrogen peroxide transportation
     
    A tank car designed for transporting hydrogen peroxide by rail

    Other sources

    Small, but detectable, amounts of hydrogen peroxide can be formed by several methods. Small amounts are formed by electrolysis of dilute acid around the cathode where hydrogen evolves if oxygen is bubbled around it. It is also produced by exposing water to ultraviolet rays from a mercury lamp, or an electric arc while confining it in a UV transparent vessel (e.g. quartz). It is detectable in ice water after burning a hydrogen gas stream aimed towards it and is also detectable on floating ice. Rapidly cooling humid air blown through an approximately 2,000 °C spark gap results in detectable amounts.[30]

    A commercially viable process to produce hydrogen peroxide directly from the environment has been of interest for many years. Efficient direct synthesis is difficult to achieve, as the reaction of hydrogen with oxygen thermodynamically favours production of water. Systems for direct synthesis have been developed, most of which employ finely dispersed metal catalysts similar to those used for hydrogenation of organic substrates.[31][32] One economic obstacle has been that direct processes give a dilute solution uneconomic for transportation. None of these has yet reached a point where it can be used for industrial-scale synthesis.

    Availability

    Hydrogen peroxide is most commonly available as a solution in water. For consumers, it is usually available from pharmacies at 3 and 6 wt% concentrations. The concentrations are sometimes described in terms of the volume of oxygen gas generated; one milliliter of a 20-volume solution generates twenty milliliters of oxygen gas when completely decomposed. For laboratory use, 30 wt% solutions are most common. Commercial grades from 70% to 98% are also available, but due to the potential of solutions of more than 68% hydrogen peroxide to be converted entirely to steam and oxygen (with the temperature of the steam increasing as the concentration increases above 68%) these grades are potentially far more hazardous and require special care in dedicated storage areas. Buyers must typically allow inspection by commercial manufacturers.

    In 1994, world production of H2O2 was around 1.9 million tonnes and grew to 2.2 million in 2006,[33] most of which was at a concentration of 70% or less. In that year, bulk 30% H2O2 sold for around 0.54 USD/kg, equivalent to US$1.50/kg (US$0.68/lb) on a "100% basis"[clarification needed].[28]

    Natural occurrence

    Hydrogen peroxide occurs in surface water, in groundwater, and in the atmosphere. It forms upon illumination or natural catalytic action by substances contained in water. Sea water contains 0.5 to 14 μg/L of hydrogen peroxide, and freshwater contains 1 to 30 μg/L.[21] Concentrations in air are about 0.4 to 4 μg/m3, varying over several orders of magnitude depending in conditions such as season, altitude, daylight and water vapor content. In rural nighttime air it is less than 0.014 μg/m3, and in moderate photochemical smog it is 14 to 42 μg/m3.[34]

    Reactions

    Decomposition

    Hydrogen peroxide decomposes to form water and oxygen with a ΔHo of –2884.5 kJ/kg[35] and a ΔS of 70.5 J/(mol·K):

     

    The rate of decomposition increases with rise in temperature, concentration, and pH (H2O2 being unstable under alkaline conditions), with cool, dilute, and acidic solutions showing the best stability. Decomposition is catalysed by various redox-active ions or compounds, including most transition metals and their compounds (e.g. manganese dioxide (MnO2), silver, and platinum).[36] Certain metal ions, such as Fe2+ or Ti3+, can cause the decomposition to take a different path, with free radicals such as the hydroxyl radical (HO) and hydroperoxyl (HOO) being formed. Potassium iodide (KI) reacts particularly rapidly and forms the basis of the elephant toothpaste demonstration. Hydrogen peroxide can also be decomposed biologically by the enzyme catalase. The decomposition of hydrogen peroxide liberates oxygen and heat; this can be dangerous, as spilling high-concentration hydrogen peroxide on a flammable substance can cause an immediate fire.

    Redox reactions

    The redox properties of hydrogen peroxide depend on pH as acidic conditions exacerbate the power of oxidizing agents and basic conditions exacerbate the power of reducing agents. As hydrogen peroxide exhibits ambivalent redox properties, being simultaneously an oxidizer or a reductant, its redox behavior immediately depends on pH.

    In acidic solutions, H2O2 is a powerful oxidizer, stronger than chlorine, chlorine dioxide, and potassium permanganate. When used for cleaning laboratory glassware, a solution of hydrogen peroxide and sulfuric acid is referred to as Piranha solution.

    H2O2 is a source of hydroxyl radicals (OH), which are highly reactive.

    Oxidizing
    reagent
    Reduced
    product
    Oxidation
    potential

    (V)
    F2 HF 3.0
    O3 O2 2.1
    H2O2 H2O 1.8
    KMnO4 MnO2 1.7
    ClO2 HClO 1.5
    Cl2 Cl 1.4

    In acidic solutions, Fe2+ is oxidized to Fe3+ (hydrogen peroxide acting as an oxidizing agent):

     

    and sulfite (SO2−3) is oxidized to sulfate (SO2−4). However, potassium permanganate is reduced to Mn2+ by acidic H2O2.

     [37]

    Under alkaline conditions, however, some of these reactions reverse; for example, Mn2+ is oxidized to Mn4+ (as MnO2).

    In basic solutions, hydrogen peroxide is a strong reductant and can reduce a variety of inorganic ions. When H2O2 acts as a reducing agent, oxygen gas is also produced. For example, hydrogen peroxide will reduce sodium hypochlorite and potassium permanganate, which is a convenient method for preparing oxygen in the laboratory:

     
     

    Organic reactions

    Hydrogen peroxide is frequently used as an oxidizing agent. Illustrative is oxidation of thioethers to sulfoxides:[38][39]

     

    Alkaline hydrogen peroxide is used for epoxidation of electron-deficient alkenes such as acrylic acid derivatives,[40] and for the oxidation of alkylboranes to alcohols, the second step of hydroboration-oxidation. It is also the principal reagent in the Dakin oxidation process.

    Precursor to other peroxide compounds

    Hydrogen peroxide is a weak acid, forming hydroperoxide or peroxide salts with many metals.

    It also converts metal oxides into the corresponding peroxides. For example, upon treatment with hydrogen peroxide, chromic acid (CrO3 and H2SO4) forms a blue peroxide CrO(O2)2.

    This kind of reaction is used industrially to produce peroxoanions. For example, reaction with borax leads to sodium perborate, a bleach used in laundry detergents:

     

    H2O2 converts carboxylic acids (RCO2H) into peroxy acids (RC(O)O2H), which are themselves used as oxidizing agents. Hydrogen peroxide reacts with acetone to form acetone peroxide and with ozone to form trioxidane. Hydrogen peroxide forms stable adducts with urea (Hydrogen peroxide - urea), sodium carbonate (sodium percarbonate) and other compounds.[41] An acid-base adduct with triphenylphosphine oxide is a useful "carrier" for H2O2 in some reactions.

    Hydrogen peroxide is both an oxidizing agent and reducing agent. The oxidation of hydrogen peroxide by sodium hypochlorite yields singlet oxygen. The net reaction of a ferric ion with hydrogen peroxide is a ferrous ion and oxygen. This proceeds via single electron oxidation and hydroxyl radicals. This is used in some organic chemistry oxidations, e.g. in the Fenton's reagent. Only catalytic quantities of iron ion is needed since peroxide also oxidizes ferrous to ferric ion. The net reaction of hydrogen peroxide and permanganate or manganese dioxide is manganous ion; however, until the peroxide is spent some manganese ions are reoxidized to make the reaction catalytic. This forms the basis for common monopropellant rockets.

    Biological function

    Hydrogen peroxide is formed in humans and other animals as a short-lived product in biochemical processes and is toxic to cells. The toxicity is due to oxidation of proteins, membrane lipids and DNA by the peroxide ions.[42] The class of biological enzymes called superoxide dismutase (SOD) is developed in nearly all living cells as an important antioxidant agent. They promote the disproportionation of superoxide into oxygen and hydrogen peroxide, which is then rapidly decomposed by the enzyme catalase to oxygen and water.[43]

     
     

    Peroxisomes are organelles found in virtually all eukaryotic cells.[44] They are involved in the catabolism of very long chain fatty acids, branched chain fatty acids, D-amino acids, polyamines, and biosynthesis of plasmalogens, ether phospholipids critical for the normal function of mammalian brains and lungs.[45] Upon oxidation, they produce hydrogen peroxide in the following process catalyzed by flavin adenine dinucleotide (FAD):[46]

     

    Catalase, another peroxisomal enzyme, uses this H2O2 to oxidize other substrates, including phenols, formic acid, formaldehyde, and alcohol, by means of a peroxidation reaction:

     

    thus eliminating the poisonous hydrogen peroxide in the process.

    This reaction is important in liver and kidney cells, where the peroxisomes neutralize various toxic substances that enter the blood. Some of the ethanol humans drink is oxidized to acetaldehyde in this way.[47] In addition, when excess H2O2 accumulates in the cell, catalase converts it to H2O through this reaction:

     

    Another origin of hydrogen peroxide is the degradation of adenosine monophosphate which yields hypoxanthine. Hypoxanthine is then oxidatively catabolized first to xanthine and then to uric acid, and the reaction is catalyzed by the enzyme xanthine oxidase:[48]

    H2O, O2
    H2O2
     
    H2O, O2
    H2O2
     
    Degradation of hypoxanthine through xanthine to uric acid to form hydrogen peroxide.
     

    The degradation of guanosine monophosphate yields xanthine as an intermediate product which is then converted in the same way to uric acid with the formation of hydrogen peroxide.[48]

    Eggs of sea urchin, shortly after fertilization by a sperm, produce hydrogen peroxide. It is then quickly dissociated to HO• radicals. The radicals serve as initiator of radical polymerization, which surrounds the eggs with a protective layer of polymer.[49]

    The bombardier beetle has a device which allows it to shoot corrosive and foul-smelling bubbles at its enemies. The beetle produces and stores hydroquinone and hydrogen peroxide, in two separate reservoirs in the rear tip of its abdomen. When threatened, the beetle contracts muscles that force the two reactants through valved tubes into a mixing chamber containing water and a mixture of catalytic enzymes. When combined, the reactants undergo a violent exothermic chemical reaction, raising the temperature to near the boiling point of water. The boiling, foul-smelling liquid partially becomes a gas (flash evaporation) and is expelled through an outlet valve with a loud popping sound.[50][51][52]

    Hydrogen peroxide is a signaling molecule of plant defense against pathogens.[53]

    Hydrogen peroxide has roles as a signalling molecule in the regulation of a wide variety of biological processes.[54] The compound is a major factor implicated in the free-radical theory of aging, based on how readily hydrogen peroxide can decompose into a hydroxyl radical and how superoxide radical byproducts of cellular metabolism can react with ambient water to form hydrogen peroxide.[55] These hydroxyl radicals in turn readily react with and damage vital cellular components, especially those of the mitochondria.[56][57][58] At least one study has also tried to link hydrogen peroxide production to cancer.[59] These studies have frequently been quoted in fraudulent treatment claims.[citation needed]

    The amount of hydrogen peroxide in biological systems can be assayed using a fluorometric assay.[60]

    Uses

    Bleaching

    About 60% of the world's production of hydrogen peroxide is used for pulp- and paper-bleaching.[33] The second major industrial application is the manufacture of sodium percarbonate and sodium perborate, which are used as mild bleaches in laundry detergents. Sodium percarbonate, which is an adduct of sodium carbonate and hydrogen peroxide, is the active ingredient in such laundry products as OxiClean and Tide laundry detergent. When dissolved in water, it releases hydrogen peroxide and sodium carbonate,[20] By themselves these bleaching agents are only effective at wash temperatures of 60 °C (140 °F) or above and so, often are used in conjunction with bleach activators, which facilitate cleaning at lower temperatures. It has also been used as a flour bleaching agent and a tooth and bone whitening agent.

    Production of organic compounds

    It is used in the production of various organic peroxides with dibenzoyl peroxide being a high volume example. Peroxy acids, such as peracetic acid and meta-chloroperoxybenzoic acid also are produced using hydrogen peroxide. Hydrogen peroxide has been used for creating organic peroxide-based explosives, such as acetone peroxide. It is used as an initiator in polymerizations.

    Sewage treatment

    Hydrogen peroxide is used in certain waste-water treatment processes to remove organic impurities. In advanced oxidation processing, the Fenton reaction[61][62] gives the highly reactive hydroxyl radical (•OH). This degrades organic compounds, including those that are ordinarily robust, such as aromatic or halogenated compounds.[63] It can also oxidize sulfur-based compounds present in the waste; which is beneficial as it generally reduces their odour.[64]

    Disinfectant

    Hydrogen peroxide may be used for the sterilization of various surfaces,[65] including surgical tools,[66] and may be deployed as a vapour (VHP) for room sterilization.[67] H2O2 demonstrates broad-spectrum efficacy against viruses, bacteria, yeasts, and bacterial spores.[68][69] In general, greater activity is seen against Gram-positive than Gram-negative bacteria; however, the presence of catalase or other peroxidases in these organisms may increase tolerance in the presence of lower concentrations.[70] Lower levels of concentration (3%) will work against most spores; higher concentrations (7 to 30%) and longer contact times will improve sporicidal activity.[69][71]

    Hydrogen peroxide is seen as an environmentally safe alternative to chlorine-based bleaches, as it degrades to form oxygen and water and it is generally recognized as safe as an antimicrobial agent by the U.S. Food and Drug Administration (FDA).[72]

    Propellant

     
    Rocket-belt hydrogen-peroxide propulsion system used in a jet pack

    High-concentration H2O2 is referred to as "high-test peroxide" (HTP). It can be used either as a monopropellant (not mixed with fuel) or as the oxidizer component of a bipropellant rocket. Use as a monopropellant takes advantage of the decomposition of 70–98% concentration hydrogen peroxide into steam and oxygen. The propellant is pumped into a reaction chamber, where a catalyst, usually a silver or platinum screen, triggers decomposition, producing steam at over 600 °C (1,100 °F), which is expelled through a nozzle, generating thrust. H2O2 monopropellant produces a maximal specific impulse (Isp) of 161 s (1.6 kN·s/kg). Peroxide was the first major monopropellant adopted for use in rocket applications. Hydrazine eventually replaced hydrogen-peroxide monopropellant thruster applications primarily because of a 25% increase in the vacuum specific impulse.[73] Hydrazine (toxic) and hydrogen peroxide (less-toxic [ACGIH TLV 0.01 and 1 ppm respectively]) are the only two monopropellants (other than cold gases) to have been widely adopted and utilized for propulsion and power applications.[citation needed] The Bell Rocket Belt, reaction control systems for X-1, X-15, Centaur, Mercury, Little Joe, as well as the turbo-pump gas generators for X-1, X-15, Jupiter, Redstone and Viking used hydrogen peroxide as a monopropellant.[74]

    As a bipropellant, H2O2 is decomposed to burn a fuel as an oxidizer. Specific impulses as high as 350 s (3.5 kN·s/kg) can be achieved, depending on the fuel. Peroxide used as an oxidizer gives a somewhat lower Isp than liquid oxygen, but is dense, storable, non-cryogenic and can be more easily used to drive gas turbines to give high pressures using an efficient closed cycle. It may also be used for regenerative cooling of rocket engines. Peroxide was used very successfully as an oxidizer in World War II German rocket motors (e.g. T-Stoff, containing oxyquinoline stabilizer, for both the Walter HWK 109-500 Starthilfe RATO externally podded monopropellant booster system, and for the Walter HWK 109-509 rocket motor series used for the Me 163B), most often used with C-Stoff in a self-igniting hypergolic combination, and for the low-cost British Black Knight and Black Arrow launchers. Presently, HTP is used on ILR-33 AMBER[75] and Nucleus[76] suborbital rockets.

    In the 1940s and 1950s, the Hellmuth Walter KG–conceived turbine used hydrogen peroxide for use in submarines while submerged; it was found to be too noisy and require too much maintenance compared to diesel-electric power systems. Some torpedoes used hydrogen peroxide as oxidizer or propellant. Operator error in the use of hydrogen-peroxide torpedoes was named as possible causes for the sinking of HMS Sidon and the Russian submarine Kursk.[77] SAAB Underwater Systems is manufacturing the Torpedo 2000. This torpedo, used by the Swedish Navy, is powered by a piston engine propelled by HTP as an oxidizer and kerosene as a fuel in a bipropellant system.[78][79]

    Household use

     
    Contact lenses soaking in a 3% hydrogen peroxide-based solution. The case includes a catalytic disc which neutralises the hydrogen peroxide over time.

    Hydrogen peroxide has various domestic uses, primarily as a cleaning and disinfecting agent.

    Hair bleaching

    Diluted H2O2 (between 1.9% and 12%) mixed with aqueous ammonia has been used to bleach human hair. The chemical's bleaching property lends its name to the phrase "peroxide blonde".[80] Hydrogen peroxide is also used for tooth whitening. It may be found in most whitening toothpastes. Hydrogen peroxide has shown positive results involving teeth lightness and chroma shade parameters.[81] It works by oxidizing colored pigments onto the enamel where the shade of the tooth may become lighter.[further explanation needed] Hydrogen peroxide may be mixed with baking soda and salt to make a homemade toothpaste.[82]

    Removal of blood stains

    Hydrogen peroxide reacts with blood as a bleaching agent, and so if a blood stain is fresh, or not too old, liberal application of hydrogen peroxide, if necessary in more than single application, will bleach the stain fully out. After about two minutes of the application, the blood should be firmly blotted out.[83][84]

    Acne treatment

    Hydrogen peroxide may be used to treat acne,[85] although benzoyl peroxide is a more common treatment.

    Niche uses

     
    Chemiluminescence of cyalume, as found in a glow stick
    Glow sticks

    Hydrogen peroxide reacts with certain di-esters, such as phenyl oxalate ester (cyalume), to produce chemiluminescence; this application is most commonly encountered in the form of glow sticks.

    Horticulture

    Some horticulturists and users of hydroponics advocate the use of weak hydrogen peroxide solution in watering solutions. Its spontaneous decomposition releases oxygen that enhances a plant's root development and helps to treat root rot (cellular root death due to lack of oxygen) and a variety of other pests.[86][87]

    For general watering concentrations around 0.1% is in use and this can be increased up to one percent for anti-fungal actions.[88] Tests show that plant foliage can safely tolerate concentrations up to 3%.[89]

    Fishkeeping

    Hydrogen peroxide is used in aquaculture for controlling mortality caused by various microbes. In 2019, the U.S. FDA approved it for control of Saprolegniasis in all coldwater finfish and all fingerling and adult coolwater and warmwater finfish, for control of external columnaris disease in warm-water finfish, and for control of Gyrodactylus spp. in freshwater-reared salmonids.[90] Laboratory tests conducted by fish culturists have demonstrated that common household hydrogen peroxide may be used safely to provide oxygen for small fish. The hydrogen peroxide releases oxygen by decomposition when it is exposed to catalysts such as manganese dioxide.

    Removing yellowing from aged plastics

    Hydrogen peroxide may be used in combination with a UV-light source to remove yellowing from white or light grey acrylonitrile butadiene styrene (ABS) plastics to partially or fully restore the original color. In the retrocomputing scene, this process is commonly referred to as retr0bright.

    Safety

     
    Skin shortly after exposure to 35% H2O2

    Regulations vary, but low concentrations, such as 5%, are widely available and legal to buy for medical use. Most over-the-counter peroxide solutions are not suitable for ingestion. Higher concentrations may be considered hazardous and typically are accompanied by a safety data sheet (SDS). In high concentrations, hydrogen peroxide is an aggressive oxidizer and will corrode many materials, including human skin. In the presence of a reducing agent, high concentrations of H2O2 will react violently.[91] While concentrations up to 35% produce only "white" oxygen bubbles in the skin (and some biting pain) that disappear with the blood within 30-45 minutes, concentrations of 98% dissolve paper. However concentrations as low as 3% can be dangerous for the eye because of oxygen evolution within the eye.[92]

    High-concentration hydrogen peroxide streams, typically above 40%, should be considered hazardous due to concentrated hydrogen peroxide's meeting the definition of a DOT oxidizer according to U.S. regulations, if released into the environment. The EPA Reportable Quantity (RQ) for D001 hazardous wastes is 100 pounds (45 kg), or approximately 10 US gallons (38 L), of concentrated hydrogen peroxide.

    Hydrogen peroxide should be stored in a cool, dry, well-ventilated area and away from any flammable or combustible substances. It should be stored in a container composed of non-reactive materials such as stainless steel or glass (other materials including some plastics and aluminium alloys may also be suitable).[93] Because it breaks down quickly when exposed to light, it should be stored in an opaque container, and pharmaceutical formulations typically come in brown bottles that block light.[94]

    Hydrogen peroxide, either in pure or diluted form, may pose several risks, the main one being that it forms explosive mixtures upon contact with organic compounds.[95] Distillation of hydrogen peroxide at normal pressures is highly dangerous. It is also corrosive, especially when concentrated, but even domestic-strength solutions may cause irritation to the eyes, mucous membranes, and skin.[96] Swallowing hydrogen peroxide solutions is particularly dangerous, as decomposition in the stomach releases large quantities of gas (ten times the volume of a 3% solution), leading to internal bloating. Inhaling over 10% can cause severe pulmonary irritation.[97]

    With a significant vapour pressure (1.2 kPa at 50 °C),[98] hydrogen-peroxide vapour is potentially hazardous. According to U.S. NIOSH, the immediately dangerous to life and health (IDLH) limit is only 75 ppm.[99] The U.S. Occupational Safety and Health Administration (OSHA) has established a permissible exposure limit of 1.0 ppm calculated as an 8-hour time-weighted average (29 CFR 1910.1000, Table Z-1).[95] Hydrogen peroxide also has been classified by the American Conference of Governmental Industrial Hygienists (ACGIH) as a "known animal carcinogen, with unknown relevance on humans".[100] For workplaces where there is a risk of exposure to the hazardous concentrations of the vapours, continuous monitors for hydrogen peroxide should be used. Information on the hazards of hydrogen peroxide is available from OSHA[95] and from the ATSDR.[101]

    Wound healing

    Historically, hydrogen peroxide was used for disinfecting wounds, partly because of its low cost and prompt availability compared to other antiseptics.[102]

    There is conflicting evidence on hydrogen peroxide's effect on wound healing. Some research finds benefit, while other research find delays and healing inhibition.[103] Its use for home treatment of wounds is generally contraindicated.[104] 1.5–3% Hydrogen peroxide is used as a desinfectant in dentistry, especially in endodotic treatments together with hypochlorite and chlorhexidin and 1–1.5% is also useful for treatment of inflammation of third molars (wisdom teeth).[105]

    Use in alternative medicine

    Practitioners of alternative medicine have advocated the use of hydrogen peroxide for various conditions, including emphysema, influenza, AIDS, and in particular cancer.[106] There is no evidence of effectiveness and in some cases it has proved fatal.[107][108][109][110][111]

    Both the effectiveness and safety of hydrogen peroxide therapy is scientifically questionable. Hydrogen peroxide is produced by the immune system, but in a carefully controlled manner. Cells called phagocytes engulf pathogens and then use hydrogen peroxide to destroy them. The peroxide is toxic to both the cell and the pathogen and so is kept within a special compartment, called a phagosome. Free hydrogen peroxide will damage any tissue it encounters via oxidative stress, a process that also has been proposed as a cause of cancer.[112] Claims that hydrogen peroxide therapy increases cellular levels of oxygen have not been supported. The quantities administered would be expected to provide very little additional oxygen compared to that available from normal respiration. It is also difficult to raise the level of oxygen around cancer cells within a tumour, as the blood supply tends to be poor, a situation known as tumor hypoxia.

    Large oral doses of hydrogen peroxide at a 3% concentration may cause irritation and blistering to the mouth, throat, and abdomen as well as abdominal pain, vomiting, and diarrhea.[107] Ingestion of hydrogen peroxide at concentrations of 35% or higher has been implicated as the cause of numerous gas embolism events resulting in hospitalisation. In these cases, hyperbaric oxygen therapy was used to treat the embolisms.[113]

    Intravenous injection of hydrogen peroxide has been linked to several deaths.[109][110][111] The American Cancer Society states that "there is no scientific evidence that hydrogen peroxide is a safe, effective, or useful cancer treatment."[108] Furthermore, the therapy is not approved by the U.S. FDA.

    Historical incidents

    • On 16 July 1934, in Kummersdorf, Germany, a propellant tank containing an experimental monopropellant mixture consisting of hydrogen peroxide and ethanol exploded during a test, killing three people.[114]
    • During the Second World War, doctors in German concentration camps experimented with the use of hydrogen peroxide injections in the killing of human subjects.[115]
    • In April 1992, an explosion occurred at the hydrogen peroxide plant at Jarrie in France, due to technical failure of the computerised control system and resulting in one fatality and wide destruction of the plant.[116]
    • Several people received minor injuries after a hydrogen peroxide spill on board a flight between the U.S. cities of Orlando and Memphis on 28 October 1998.[117]
    • The Russian submarine K-141 Kursk sailed to perform an exercise of firing dummy torpedoes at the Pyotr Velikiy, a Kirov-class battlecruiser. On 12 August 2000, at 11:28 local time (07:28 UTC), there was an explosion while preparing to fire the torpedoes. The only credible report to date is that this was due to the failure and explosion of one of the Kursk's hydrogen peroxide-fueled torpedoes. It is believed that HTP, a form of highly concentrated hydrogen peroxide used as propellant for the torpedo, seeped through its container, damaged either by rust or in the loading procedure back on land where an incident involving one of the torpedoes accidentally touching ground went unreported. The vessel was lost with all hands. A similar incident was responsible for the loss of HMS Sidon in 1955.[118]
    • On 15 August 2010, a spill of about 30 US gallons (110 L) of cleaning fluid occurred on the 54th floor of 1515 Broadway, in Times Square, New York City. The spill, which a spokesperson for the New York City fire department said was of hydrogen peroxide, shut down Broadway between West 42nd and West 48th streets as fire engines responded to the hazmat situation. There were no reported injuries.[119]

    See also

    References

    Notes

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    Bibliography

    • DrabowiczJ, et al. (1994). Capozzi G, et al. (eds.). The Syntheses of Sulphones, Sulphoxides and Cyclic Sulphides. Chichester UK: John Wiley & Sons. pp. 112–6. ISBN 978-0-471-93970-2.
    • Greenwood NN, Earnshaw A (1997). Chemistry of the Elements (2nd ed.). Oxford UK: Butterworth-Heinemann. A great description of properties & chemistry of H2O2.
    • March J (1992). Advanced Organic Chemistry (4th ed.). New York: Wiley. p. 723.
    • Hess WT (1995). "Hydrogen Peroxide". Kirk-Othmer Encyclopedia of Chemical Technology. Vol. 13 (4th ed.). New York: Wiley. pp. 961–995.

    External links

    • Hydrogen Peroxide at The Periodic Table of Videos (University of Nottingham)
    • International Chemical Safety Card 0164
    • NIOSH Pocket Guide to Chemical Hazards
    • Hydrogen Peroxide Handbook by Rocketdyne
    • IR spectroscopic study J. Phys. Chem.

    hydrogen, peroxide, chemical, compound, with, formula, h2o2, pure, form, very, pale, blue, liquid, that, slightly, more, viscous, than, water, used, oxidizer, bleaching, agent, antiseptic, usually, dilute, solution, weight, water, consumer, higher, concentrati. Hydrogen peroxide is a chemical compound with the formula H2O2 In its pure form it is a very pale blue 5 liquid that is slightly more viscous than water It is used as an oxidizer bleaching agent and antiseptic usually as a dilute solution 3 6 by weight in water for consumer use and in higher concentrations for industrial use Concentrated hydrogen peroxide or high test peroxide decomposes explosively when heated and has been used as a propellant in rocketry 6 Hydrogen peroxide Ball stick model of the hydrogen peroxide moleculeNamesIUPAC name Hydrogen peroxideOther names DioxidaneOxidanylPerhydroxic acid0 hydroxyolDihydrogen dioxideOxygenated waterPeroxaanIdentifiersCAS Number 7722 84 1 Y3D model JSmol Interactive imageChEBI CHEBI 16240 YChEMBL ChEMBL71595 YChemSpider 763 YECHA InfoCard 100 028 878EC Number 231 765 0IUPHAR BPS 2448KEGG D00008 YPubChem CID 784RTECS number MX0900000 gt 90 soln MX0887000 gt 30 soln UNII BBX060AN9V YUN number 2015 gt 60 soln 2014 20 60 soln 2984 8 20 soln CompTox Dashboard EPA DTXSID2020715InChI InChI 1S H2O2 c1 2 h1 2H YKey MHAJPDPJQMAIIY UHFFFAOYSA N YInChI 1 H2O2 c1 2 h1 2HKey MHAJPDPJQMAIIY UHFFFAOYALSMILES OOPropertiesChemical formula H2O2Molar mass 34 0147 g molAppearance Very light blue liquidOdor slightly sharpDensity 1 11 g cm3 20 C 30 w w solution 1 1 450 g cm3 20 C pure Melting point 0 43 C 31 23 F 272 72 K Boiling point 150 2 C 302 4 F 423 3 K decomposes Solubility in water MiscibleSolubility soluble in ether alcohol insoluble in petroleum etherlog P 0 43 2 Vapor pressure 5 mmHg 30 C 3 Acidity pKa 11 75Magnetic susceptibility x 17 7 10 6 cm3 molRefractive index nD 1 4061Viscosity 1 245 cP 20 C Dipole moment 2 26 DThermochemistryHeat capacity C 1 267 J g K gas 2 619 J g K liquid Std enthalpy offormation DfH 298 187 80 kJ molPharmacologyATC code A01AB02 WHO D08AX01 WHO D11AX25 WHO S02AA06 WHO HazardsGHS labelling PictogramsSignal word DangerHazard statements H271 H302 H314 H332 H335 H412Precautionary statements P280 P305 P351 P338 P310NFPA 704 fire diamond 303OXFlash point Non flammableLethal dose or concentration LD LC LD50 median dose 1518 mg kg citation needed 2000 mg kg oral mouse 4 LC50 median concentration 1418 ppm rat 4 hr 4 LCLo lowest published 227 ppm mouse 4 NIOSH US health exposure limits PEL Permissible TWA 1 ppm 1 4 mg m3 3 REL Recommended TWA 1 ppm 1 4 mg m3 3 IDLH Immediate danger 75 ppm 3 Safety data sheet SDS ICSC 0164 gt 60 soln Related compoundsRelated compounds WaterOzoneHydrazineHydrogen disulfideDioxygen difluorideExcept where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa Y verify what is Y N Infobox references Hydrogen peroxide is a reactive oxygen species and the simplest peroxide a compound having an oxygen oxygen single bond It decomposes slowly into water and elemental oxygen when exposed to light and rapidly in the presence of organic or reactive compounds It is typically stored with a stabilizer in a weakly acidic solution in a dark bottle to block light Hydrogen peroxide is found in biological systems including the human body Enzymes that use or decompose hydrogen peroxide are classified as peroxidases Contents 1 Properties 1 1 Structure 1 2 Aqueous solutions 1 3 Comparison with analogues 2 Discovery 3 Production 3 1 Other sources 3 2 Availability 3 3 Natural occurrence 4 Reactions 4 1 Decomposition 4 2 Redox reactions 4 3 Organic reactions 4 4 Precursor to other peroxide compounds 5 Biological function 6 Uses 6 1 Bleaching 6 2 Production of organic compounds 6 3 Sewage treatment 6 4 Disinfectant 6 5 Propellant 6 6 Household use 6 7 Niche uses 7 Safety 7 1 Wound healing 7 2 Use in alternative medicine 7 3 Historical incidents 8 See also 9 References 10 External linksProperties EditThe boiling point of H2O2 has been extrapolated as being 150 2 C 302 4 F approximately 50 C 90 F higher than water In practice hydrogen peroxide will undergo potentially explosive thermal decomposition if heated to this temperature It may be safely distilled at lower temperatures under reduced pressure 7 Structure Edit Structure and dimensions of H2O2 in the gas phase Structure and dimensions of H2O2 in the solid crystalline phase Hydrogen peroxide H2O2 is a nonplanar molecule with twisted C2 symmetry this was first shown by Paul Antoine Giguere in 1950 using infrared spectroscopy 8 9 Although the O O bond is a single bond the molecule has a relatively high rotational barrier of 386 cm 1 4 62 kJ mol for rotation between enantiomers via the trans configuration and 2460 cm 1 29 4 kJ mol via the cis configuration 10 These barriers are proposed to be due to repulsion between the lone pairs of the adjacent oxygen atoms and dipolar effects between the two O H bonds For comparison the rotational barrier for ethane is 1040 cm 1 12 4 kJ mol The approximately 100 dihedral angle between the two O H bonds makes the molecule chiral It is the smallest and simplest molecule to exhibit enantiomerism It has been proposed that the enantiospecific interactions of one rather than the other may have led to amplification of one enantiomeric form of ribonucleic acids and therefore an origin of homochirality in an RNA world 11 The molecular structures of gaseous and crystalline H2O2 are significantly different This difference is attributed to the effects of hydrogen bonding which is absent in the gaseous state 12 Crystals of H2O2 are tetragonal with the space group D44 or P41212 13 Aqueous solutions Edit In aqueous solutions hydrogen peroxide differs from the pure substance due to the effects of hydrogen bonding between water and hydrogen peroxide molecules Hydrogen peroxide and water form a eutectic mixture exhibiting freezing point depression down as low as 56 C pure water has a freezing point of 0 C and pure hydrogen peroxide of 0 43 C The boiling point of the same mixtures is also depressed in relation with the mean of both boiling points 125 1 C It occurs at 114 C This boiling point is 14 C greater than that of pure water and 36 2 C less than that of pure hydrogen peroxide 14 Phase diagram of H2O2 and water Area above blue line is liquid Dotted lines separate solid liquid phases from solid solid phases Density of aqueous solution of H2O2 H2O2 w w Density g cm3 Temp C 3 1 0095 1527 1 10 2035 1 13 2050 1 20 2070 1 29 2075 1 33 2096 1 42 2098 1 43 20100 1 45 20 Comparison with analogues Edit Hydrogen peroxide has several structural analogues with HmX XHn bonding arrangements water also shown for comparison It has the highest theoretical boiling point of this series X O S N P Its melting point is also fairly high being comparable to that of hydrazine and water with only hydroxylamine crystallising significantly more readily indicative of particularly strong hydrogen bonding Diphosphane and hydrogen disulfide exhibit only weak hydrogen bonding and have little chemical similarity to hydrogen peroxide Structurally the analogues all adopt similar skewed structures due to repulsion between adjacent lone pairs Properties of H2O2 and its analoguesValues marked are extrapolated Name Formula Molar mass g mol Meltingpoint C Boilingpoint C Water HOH 18 02 0 00 99 98Hydrogen peroxide HOOH 34 01 0 43 150 2 Hydrogen disulfide HSSH 66 15 89 6 70 7Hydrazine H2NNH2 32 05 2 114Hydroxylamine NH2OH 33 03 33 58 Diphosphane H2PPH2 65 98 99 63 5 Discovery EditAlexander von Humboldt is sometimes said to have been the first to report the first synthetic peroxide barium peroxide in 1799 as a by product of his attempts to decompose air although this is disputed due to von Humboldt s ambiguous wording 15 Nineteen years later Louis Jacques Thenard recognized that this compound could be used for the preparation of a previously unknown compound which he described as eau oxygenee oxygenated water subsequently known as hydrogen peroxide 16 17 18 Today the term oxygenated water may appear on retail packaging referring to mixtures containing either water and hydrogen peroxide or water and dissolved oxygen This could cause personal injury if the difference is not properly understood by the user 19 An improved version of Thenard s process used hydrochloric acid followed by addition of sulfuric acid to precipitate the barium sulfate byproduct This process was used from the end of the 19th century until the middle of the 20th century 20 The bleaching effect of peroxides and their salts on natural dyes had been known since Thenard s experiments in the 1820s but early attempts of industrial production of peroxides failed The first plant producing hydrogen peroxide was built in 1873 in Berlin The discovery of the synthesis of hydrogen peroxide by electrolysis with sulfuric acid introduced the more efficient electrochemical method It was first commercialized in 1908 in Weissenstein Carinthia Austria The anthraquinone process which is still used was developed during the 1930s by the German chemical manufacturer IG Farben in Ludwigshafen The increased demand and improvements in the synthesis methods resulted in the rise of the annual production of hydrogen peroxide from 35 000 tonnes in 1950 to over 100 000 tonnes in 1960 to 300 000 tonnes by 1970 by 1998 it reached 2 7 million tonnes 21 Early attempts failed to produce neat hydrogen peroxide Anhydrous hydrogen peroxide was first obtained by vacuum distillation 22 Determination of the molecular structure of hydrogen peroxide proved to be very difficult In 1892 the Italian physical chemist Giacomo Carrara 1864 1925 determined its molecular mass by freezing point depression which confirmed that its molecular formula is H2O2 23 H2O O seemed to be just as possible as the modern structure and as late as in the middle of the 20th century at least half a dozen hypothetical isomeric variants of two main options seemed to be consistent with the available evidence 24 In 1934 the English mathematical physicist William Penney and the Scottish physicist Gordon Sutherland proposed a molecular structure for hydrogen peroxide that was very similar to the presently accepted one 25 26 Previously hydrogen peroxide was prepared industrially by hydrolysis of ammonium persulfate NH 4 2 S 2 O 8 2 H 2 O 2 NH 4 HSO 4 H 2 O 2 displaystyle ce NH4 2S2O8 2 H2O gt 2 NH4 HSO4 H2O2 which was itself obtained by the electrolysis of a solution of ammonium bisulfate NH4 HSO4 in sulfuric acid 27 2 NH 4 HSO 4 NH 4 2 S 2 O 8 H 2 displaystyle ce 2 NH4 HSO4 gt NH4 2S2O8 H2 Production Edit Catalytic cycle for the anthraquinone process to produce hydrogen peroxide an anthraquinone right is reduced using hydrogen to produce the corresponding anthrahydroquinone left This is oxidized using oxygen to produce hydrogen peroxide and recover anthraquinone Today hydrogen peroxide is manufactured almost exclusively by the anthraquinone process which was originally developed by BASF in 1939 It begins with the reduction of an anthraquinone such as 2 ethylanthraquinone or the 2 amyl derivative to the corresponding anthrahydroquinone typically by hydrogenation on a palladium catalyst In the presence of oxygen the anthrahydroquinone then undergoes autoxidation the labile hydrogen atoms of the hydroxy groups transfer to the oxygen molecule to give hydrogen peroxide and regenerating the anthraquinone Most commercial processes achieve oxidation by bubbling compressed air through a solution of the anthrahydroquinone with the hydrogen peroxide then extracted from the solution and the anthraquinone recycled back for successive cycles of hydrogenation and oxidation 28 29 The net reaction for the anthraquinone catalyzed process is 28 H2 O2 H2O2The economics of the process depend heavily on effective recycling of the extraction solvents the hydrogenation catalyst and the expensive quinone ISO tank container for hydrogen peroxide transportation A tank car designed for transporting hydrogen peroxide by rail Other sources Edit Small but detectable amounts of hydrogen peroxide can be formed by several methods Small amounts are formed by electrolysis of dilute acid around the cathode where hydrogen evolves if oxygen is bubbled around it It is also produced by exposing water to ultraviolet rays from a mercury lamp or an electric arc while confining it in a UV transparent vessel e g quartz It is detectable in ice water after burning a hydrogen gas stream aimed towards it and is also detectable on floating ice Rapidly cooling humid air blown through an approximately 2 000 C spark gap results in detectable amounts 30 A commercially viable process to produce hydrogen peroxide directly from the environment has been of interest for many years Efficient direct synthesis is difficult to achieve as the reaction of hydrogen with oxygen thermodynamically favours production of water Systems for direct synthesis have been developed most of which employ finely dispersed metal catalysts similar to those used for hydrogenation of organic substrates 31 32 One economic obstacle has been that direct processes give a dilute solution uneconomic for transportation None of these has yet reached a point where it can be used for industrial scale synthesis Availability Edit Hydrogen peroxide is most commonly available as a solution in water For consumers it is usually available from pharmacies at 3 and 6 wt concentrations The concentrations are sometimes described in terms of the volume of oxygen gas generated one milliliter of a 20 volume solution generates twenty milliliters of oxygen gas when completely decomposed For laboratory use 30 wt solutions are most common Commercial grades from 70 to 98 are also available but due to the potential of solutions of more than 68 hydrogen peroxide to be converted entirely to steam and oxygen with the temperature of the steam increasing as the concentration increases above 68 these grades are potentially far more hazardous and require special care in dedicated storage areas Buyers must typically allow inspection by commercial manufacturers In 1994 world production of H2O2 was around 1 9 million tonnes and grew to 2 2 million in 2006 33 most of which was at a concentration of 70 or less In that year bulk 30 H2O2 sold for around 0 54 USD kg equivalent to US 1 50 kg US 0 68 lb on a 100 basis clarification needed 28 Natural occurrence Edit Hydrogen peroxide occurs in surface water in groundwater and in the atmosphere It forms upon illumination or natural catalytic action by substances contained in water Sea water contains 0 5 to 14 mg L of hydrogen peroxide and freshwater contains 1 to 30 mg L 21 Concentrations in air are about 0 4 to 4 mg m3 varying over several orders of magnitude depending in conditions such as season altitude daylight and water vapor content In rural nighttime air it is less than 0 014 mg m3 and in moderate photochemical smog it is 14 to 42 mg m3 34 Reactions EditDecomposition Edit Hydrogen peroxide decomposes to form water and oxygen with a DHo of 2884 5 kJ kg 35 and a DS of 70 5 J mol K 2 H 2 O 2 2 H 2 O O 2 displaystyle ce 2 H2O2 gt 2 H2O O2 The rate of decomposition increases with rise in temperature concentration and pH H2O2 being unstable under alkaline conditions with cool dilute and acidic solutions showing the best stability Decomposition is catalysed by various redox active ions or compounds including most transition metals and their compounds e g manganese dioxide MnO2 silver and platinum 36 Certain metal ions such as Fe2 or Ti3 can cause the decomposition to take a different path with free radicals such as the hydroxyl radical HO and hydroperoxyl HOO being formed Potassium iodide KI reacts particularly rapidly and forms the basis of the elephant toothpaste demonstration Hydrogen peroxide can also be decomposed biologically by the enzyme catalase The decomposition of hydrogen peroxide liberates oxygen and heat this can be dangerous as spilling high concentration hydrogen peroxide on a flammable substance can cause an immediate fire Redox reactions Edit The redox properties of hydrogen peroxide depend on pH as acidic conditions exacerbate the power of oxidizing agents and basic conditions exacerbate the power of reducing agents As hydrogen peroxide exhibits ambivalent redox properties being simultaneously an oxidizer or a reductant its redox behavior immediately depends on pH In acidic solutions H2O2 is a powerful oxidizer stronger than chlorine chlorine dioxide and potassium permanganate When used for cleaning laboratory glassware a solution of hydrogen peroxide and sulfuric acid is referred to as Piranha solution H2O2 is a source of hydroxyl radicals OH which are highly reactive Oxidizingreagent Reducedproduct Oxidationpotential V F2 HF 3 0O3 O2 2 1H2O2 H2O 1 8KMnO4 MnO2 1 7ClO2 HClO 1 5Cl2 Cl 1 4In acidic solutions Fe2 is oxidized to Fe3 hydrogen peroxide acting as an oxidizing agent 2 Fe aq 2 H 2 O 2 2 H aq 2 Fe aq 3 2 H 2 O l displaystyle ce 2 Fe 2 aq H2O2 2 H aq gt 2 Fe 3 aq 2 H2O l and sulfite SO2 3 is oxidized to sulfate SO2 4 However potassium permanganate is reduced to Mn2 by acidic H2O2 2 MnO 4 5 H 2 O 2 6 H 2 Mn 2 8 H 2 O 5 O 2 displaystyle ce 2 MnO4 5 H2O2 6 H gt 2 Mn 2 8 H2O 5 O2 37 Under alkaline conditions however some of these reactions reverse for example Mn2 is oxidized to Mn4 as MnO2 In basic solutions hydrogen peroxide is a strong reductant and can reduce a variety of inorganic ions When H2O2 acts as a reducing agent oxygen gas is also produced For example hydrogen peroxide will reduce sodium hypochlorite and potassium permanganate which is a convenient method for preparing oxygen in the laboratory NaOCl H 2 O 2 O 2 NaCl H 2 O displaystyle ce NaOCl H2O2 gt O2 NaCl H2O 2 KMnO 4 3 H 2 O 2 2 MnO 2 2 KOH 2 H 2 O 3 O 2 displaystyle ce 2 KMnO4 3 H2O2 gt 2 MnO2 2 KOH 2 H2O 3 O2 Organic reactions Edit Hydrogen peroxide is frequently used as an oxidizing agent Illustrative is oxidation of thioethers to sulfoxides 38 39 Ph S CH 3 H 2 O 2 Ph S O CH 3 H 2 O displaystyle ce Ph S CH3 H2O2 gt Ph S O CH3 H2O Alkaline hydrogen peroxide is used for epoxidation of electron deficient alkenes such as acrylic acid derivatives 40 and for the oxidation of alkylboranes to alcohols the second step of hydroboration oxidation It is also the principal reagent in the Dakin oxidation process Precursor to other peroxide compounds Edit Hydrogen peroxide is a weak acid forming hydroperoxide or peroxide salts with many metals It also converts metal oxides into the corresponding peroxides For example upon treatment with hydrogen peroxide chromic acid CrO3 and H2SO4 forms a blue peroxide CrO O2 2 This kind of reaction is used industrially to produce peroxoanions For example reaction with borax leads to sodium perborate a bleach used in laundry detergents Na 2 B 4 O 7 4 H 2 O 2 2 NaOH 2 Na 2 B 2 O 4 OH 4 H 2 O displaystyle ce Na2B4O7 4 H2O2 2 NaOH gt 2 Na2B2O4 OH 4 H2O H2O2 converts carboxylic acids RCO2H into peroxy acids RC O O2H which are themselves used as oxidizing agents Hydrogen peroxide reacts with acetone to form acetone peroxide and with ozone to form trioxidane Hydrogen peroxide forms stable adducts with urea Hydrogen peroxide urea sodium carbonate sodium percarbonate and other compounds 41 An acid base adduct with triphenylphosphine oxide is a useful carrier for H2O2 in some reactions Hydrogen peroxide is both an oxidizing agent and reducing agent The oxidation of hydrogen peroxide by sodium hypochlorite yields singlet oxygen The net reaction of a ferric ion with hydrogen peroxide is a ferrous ion and oxygen This proceeds via single electron oxidation and hydroxyl radicals This is used in some organic chemistry oxidations e g in the Fenton s reagent Only catalytic quantities of iron ion is needed since peroxide also oxidizes ferrous to ferric ion The net reaction of hydrogen peroxide and permanganate or manganese dioxide is manganous ion however until the peroxide is spent some manganese ions are reoxidized to make the reaction catalytic This forms the basis for common monopropellant rockets Biological function Edit Ascaridole Hydrogen peroxide is formed in humans and other animals as a short lived product in biochemical processes and is toxic to cells The toxicity is due to oxidation of proteins membrane lipids and DNA by the peroxide ions 42 The class of biological enzymes called superoxide dismutase SOD is developed in nearly all living cells as an important antioxidant agent They promote the disproportionation of superoxide into oxygen and hydrogen peroxide which is then rapidly decomposed by the enzyme catalase to oxygen and water 43 2 O 2 2 H O 2 H 2 O 2 displaystyle ce 2 O2 2 H gt O2 H2O2 2 H 2 O 2 O 2 2 H 2 O displaystyle ce 2 H2O2 gt O2 2 H2O Peroxisomes are organelles found in virtually all eukaryotic cells 44 They are involved in the catabolism of very long chain fatty acids branched chain fatty acids D amino acids polyamines and biosynthesis of plasmalogens ether phospholipids critical for the normal function of mammalian brains and lungs 45 Upon oxidation they produce hydrogen peroxide in the following process catalyzed by flavin adenine dinucleotide FAD 46 R CH 2 CH 2 CO SCoA O 2 FAD R CH CH CO SCoA H 2 O 2 displaystyle ce R CH2 CH2 CO SCoA O2 gt ce FAD R CH CH CO SCoA H2O2 Catalase another peroxisomal enzyme uses this H2O2 to oxidize other substrates including phenols formic acid formaldehyde and alcohol by means of a peroxidation reaction H 2 O 2 R H 2 R 2 H 2 O displaystyle ce H2O2 R H2 gt R 2 H2O thus eliminating the poisonous hydrogen peroxide in the process This reaction is important in liver and kidney cells where the peroxisomes neutralize various toxic substances that enter the blood Some of the ethanol humans drink is oxidized to acetaldehyde in this way 47 In addition when excess H2O2 accumulates in the cell catalase converts it to H2O through this reaction H 2 O 2 CAT 1 2 O 2 H 2 O displaystyle ce H2O2 gt ce CAT 1 2O2 H2O Another origin of hydrogen peroxide is the degradation of adenosine monophosphate which yields hypoxanthine Hypoxanthine is then oxidatively catabolized first to xanthine and then to uric acid and the reaction is catalyzed by the enzyme xanthine oxidase 48 Hypoxanthine Xanthine oxidaseH2O O2 H2O2 Xanthine Xanthine oxidaseH2O O2 H2O2 Uric acid Degradation of hypoxanthine through xanthine to uric acid to form hydrogen peroxide Australian bombardier beetle The degradation of guanosine monophosphate yields xanthine as an intermediate product which is then converted in the same way to uric acid with the formation of hydrogen peroxide 48 Eggs of sea urchin shortly after fertilization by a sperm produce hydrogen peroxide It is then quickly dissociated to HO radicals The radicals serve as initiator of radical polymerization which surrounds the eggs with a protective layer of polymer 49 The bombardier beetle has a device which allows it to shoot corrosive and foul smelling bubbles at its enemies The beetle produces and stores hydroquinone and hydrogen peroxide in two separate reservoirs in the rear tip of its abdomen When threatened the beetle contracts muscles that force the two reactants through valved tubes into a mixing chamber containing water and a mixture of catalytic enzymes When combined the reactants undergo a violent exothermic chemical reaction raising the temperature to near the boiling point of water The boiling foul smelling liquid partially becomes a gas flash evaporation and is expelled through an outlet valve with a loud popping sound 50 51 52 Hydrogen peroxide is a signaling molecule of plant defense against pathogens 53 Hydrogen peroxide has roles as a signalling molecule in the regulation of a wide variety of biological processes 54 The compound is a major factor implicated in the free radical theory of aging based on how readily hydrogen peroxide can decompose into a hydroxyl radical and how superoxide radical byproducts of cellular metabolism can react with ambient water to form hydrogen peroxide 55 These hydroxyl radicals in turn readily react with and damage vital cellular components especially those of the mitochondria 56 57 58 At least one study has also tried to link hydrogen peroxide production to cancer 59 These studies have frequently been quoted in fraudulent treatment claims citation needed The amount of hydrogen peroxide in biological systems can be assayed using a fluorometric assay 60 Uses EditBleaching Edit About 60 of the world s production of hydrogen peroxide is used for pulp and paper bleaching 33 The second major industrial application is the manufacture of sodium percarbonate and sodium perborate which are used as mild bleaches in laundry detergents Sodium percarbonate which is an adduct of sodium carbonate and hydrogen peroxide is the active ingredient in such laundry products as OxiClean and Tide laundry detergent When dissolved in water it releases hydrogen peroxide and sodium carbonate 20 By themselves these bleaching agents are only effective at wash temperatures of 60 C 140 F or above and so often are used in conjunction with bleach activators which facilitate cleaning at lower temperatures It has also been used as a flour bleaching agent and a tooth and bone whitening agent Production of organic compounds Edit It is used in the production of various organic peroxides with dibenzoyl peroxide being a high volume example Peroxy acids such as peracetic acid and meta chloroperoxybenzoic acid also are produced using hydrogen peroxide Hydrogen peroxide has been used for creating organic peroxide based explosives such as acetone peroxide It is used as an initiator in polymerizations Sewage treatment Edit Hydrogen peroxide is used in certain waste water treatment processes to remove organic impurities In advanced oxidation processing the Fenton reaction 61 62 gives the highly reactive hydroxyl radical OH This degrades organic compounds including those that are ordinarily robust such as aromatic or halogenated compounds 63 It can also oxidize sulfur based compounds present in the waste which is beneficial as it generally reduces their odour 64 Disinfectant Edit Hydrogen peroxide may be used for the sterilization of various surfaces 65 including surgical tools 66 and may be deployed as a vapour VHP for room sterilization 67 H2O2 demonstrates broad spectrum efficacy against viruses bacteria yeasts and bacterial spores 68 69 In general greater activity is seen against Gram positive than Gram negative bacteria however the presence of catalase or other peroxidases in these organisms may increase tolerance in the presence of lower concentrations 70 Lower levels of concentration 3 will work against most spores higher concentrations 7 to 30 and longer contact times will improve sporicidal activity 69 71 Hydrogen peroxide is seen as an environmentally safe alternative to chlorine based bleaches as it degrades to form oxygen and water and it is generally recognized as safe as an antimicrobial agent by the U S Food and Drug Administration FDA 72 Propellant Edit Further information High test peroxide Rocket belt hydrogen peroxide propulsion system used in a jet pack High concentration H2O2 is referred to as high test peroxide HTP It can be used either as a monopropellant not mixed with fuel or as the oxidizer component of a bipropellant rocket Use as a monopropellant takes advantage of the decomposition of 70 98 concentration hydrogen peroxide into steam and oxygen The propellant is pumped into a reaction chamber where a catalyst usually a silver or platinum screen triggers decomposition producing steam at over 600 C 1 100 F which is expelled through a nozzle generating thrust H2O2 monopropellant produces a maximal specific impulse Isp of 161 s 1 6 kN s kg Peroxide was the first major monopropellant adopted for use in rocket applications Hydrazine eventually replaced hydrogen peroxide monopropellant thruster applications primarily because of a 25 increase in the vacuum specific impulse 73 Hydrazine toxic and hydrogen peroxide less toxic ACGIH TLV 0 01 and 1 ppm respectively are the only two monopropellants other than cold gases to have been widely adopted and utilized for propulsion and power applications citation needed The Bell Rocket Belt reaction control systems for X 1 X 15 Centaur Mercury Little Joe as well as the turbo pump gas generators for X 1 X 15 Jupiter Redstone and Viking used hydrogen peroxide as a monopropellant 74 As a bipropellant H2O2 is decomposed to burn a fuel as an oxidizer Specific impulses as high as 350 s 3 5 kN s kg can be achieved depending on the fuel Peroxide used as an oxidizer gives a somewhat lower Isp than liquid oxygen but is dense storable non cryogenic and can be more easily used to drive gas turbines to give high pressures using an efficient closed cycle It may also be used for regenerative cooling of rocket engines Peroxide was used very successfully as an oxidizer in World War II German rocket motors e g T Stoff containing oxyquinoline stabilizer for both the Walter HWK 109 500 Starthilfe RATO externally podded monopropellant booster system and for the Walter HWK 109 509 rocket motor series used for the Me 163B most often used with C Stoff in a self igniting hypergolic combination and for the low cost British Black Knight and Black Arrow launchers Presently HTP is used on ILR 33 AMBER 75 and Nucleus 76 suborbital rockets In the 1940s and 1950s the Hellmuth Walter KG conceived turbine used hydrogen peroxide for use in submarines while submerged it was found to be too noisy and require too much maintenance compared to diesel electric power systems Some torpedoes used hydrogen peroxide as oxidizer or propellant Operator error in the use of hydrogen peroxide torpedoes was named as possible causes for the sinking of HMS Sidon and the Russian submarine Kursk 77 SAAB Underwater Systems is manufacturing the Torpedo 2000 This torpedo used by the Swedish Navy is powered by a piston engine propelled by HTP as an oxidizer and kerosene as a fuel in a bipropellant system 78 79 Household use Edit Contact lenses soaking in a 3 hydrogen peroxide based solution The case includes a catalytic disc which neutralises the hydrogen peroxide over time Hydrogen peroxide has various domestic uses primarily as a cleaning and disinfecting agent Hair bleachingDiluted H2O2 between 1 9 and 12 mixed with aqueous ammonia has been used to bleach human hair The chemical s bleaching property lends its name to the phrase peroxide blonde 80 Hydrogen peroxide is also used for tooth whitening It may be found in most whitening toothpastes Hydrogen peroxide has shown positive results involving teeth lightness and chroma shade parameters 81 It works by oxidizing colored pigments onto the enamel where the shade of the tooth may become lighter further explanation needed Hydrogen peroxide may be mixed with baking soda and salt to make a homemade toothpaste 82 Removal of blood stainsHydrogen peroxide reacts with blood as a bleaching agent and so if a blood stain is fresh or not too old liberal application of hydrogen peroxide if necessary in more than single application will bleach the stain fully out After about two minutes of the application the blood should be firmly blotted out 83 84 Acne treatmentHydrogen peroxide may be used to treat acne 85 although benzoyl peroxide is a more common treatment Niche uses Edit Chemiluminescence of cyalume as found in a glow stick Glow sticksHydrogen peroxide reacts with certain di esters such as phenyl oxalate ester cyalume to produce chemiluminescence this application is most commonly encountered in the form of glow sticks HorticultureSome horticulturists and users of hydroponics advocate the use of weak hydrogen peroxide solution in watering solutions Its spontaneous decomposition releases oxygen that enhances a plant s root development and helps to treat root rot cellular root death due to lack of oxygen and a variety of other pests 86 87 For general watering concentrations around 0 1 is in use and this can be increased up to one percent for anti fungal actions 88 Tests show that plant foliage can safely tolerate concentrations up to 3 89 FishkeepingHydrogen peroxide is used in aquaculture for controlling mortality caused by various microbes In 2019 the U S FDA approved it for control of Saprolegniasis in all coldwater finfish and all fingerling and adult coolwater and warmwater finfish for control of external columnaris disease in warm water finfish and for control of Gyrodactylus spp in freshwater reared salmonids 90 Laboratory tests conducted by fish culturists have demonstrated that common household hydrogen peroxide may be used safely to provide oxygen for small fish The hydrogen peroxide releases oxygen by decomposition when it is exposed to catalysts such as manganese dioxide Removing yellowing from aged plasticsHydrogen peroxide may be used in combination with a UV light source to remove yellowing from white or light grey acrylonitrile butadiene styrene ABS plastics to partially or fully restore the original color In the retrocomputing scene this process is commonly referred to as retr0bright Safety Edit Skin shortly after exposure to 35 H2O2 Regulations vary but low concentrations such as 5 are widely available and legal to buy for medical use Most over the counter peroxide solutions are not suitable for ingestion Higher concentrations may be considered hazardous and typically are accompanied by a safety data sheet SDS In high concentrations hydrogen peroxide is an aggressive oxidizer and will corrode many materials including human skin In the presence of a reducing agent high concentrations of H2O2 will react violently 91 While concentrations up to 35 produce only white oxygen bubbles in the skin and some biting pain that disappear with the blood within 30 45 minutes concentrations of 98 dissolve paper However concentrations as low as 3 can be dangerous for the eye because of oxygen evolution within the eye 92 High concentration hydrogen peroxide streams typically above 40 should be considered hazardous due to concentrated hydrogen peroxide s meeting the definition of a DOT oxidizer according to U S regulations if released into the environment The EPA Reportable Quantity RQ for D001 hazardous wastes is 100 pounds 45 kg or approximately 10 US gallons 38 L of concentrated hydrogen peroxide Hydrogen peroxide should be stored in a cool dry well ventilated area and away from any flammable or combustible substances It should be stored in a container composed of non reactive materials such as stainless steel or glass other materials including some plastics and aluminium alloys may also be suitable 93 Because it breaks down quickly when exposed to light it should be stored in an opaque container and pharmaceutical formulations typically come in brown bottles that block light 94 Hydrogen peroxide either in pure or diluted form may pose several risks the main one being that it forms explosive mixtures upon contact with organic compounds 95 Distillation of hydrogen peroxide at normal pressures is highly dangerous It is also corrosive especially when concentrated but even domestic strength solutions may cause irritation to the eyes mucous membranes and skin 96 Swallowing hydrogen peroxide solutions is particularly dangerous as decomposition in the stomach releases large quantities of gas ten times the volume of a 3 solution leading to internal bloating Inhaling over 10 can cause severe pulmonary irritation 97 With a significant vapour pressure 1 2 kPa at 50 C 98 hydrogen peroxide vapour is potentially hazardous According to U S NIOSH the immediately dangerous to life and health IDLH limit is only 75 ppm 99 The U S Occupational Safety and Health Administration OSHA has established a permissible exposure limit of 1 0 ppm calculated as an 8 hour time weighted average 29 CFR 1910 1000 Table Z 1 95 Hydrogen peroxide also has been classified by the American Conference of Governmental Industrial Hygienists ACGIH as a known animal carcinogen with unknown relevance on humans 100 For workplaces where there is a risk of exposure to the hazardous concentrations of the vapours continuous monitors for hydrogen peroxide should be used Information on the hazards of hydrogen peroxide is available from OSHA 95 and from the ATSDR 101 Wound healing Edit Historically hydrogen peroxide was used for disinfecting wounds partly because of its low cost and prompt availability compared to other antiseptics 102 There is conflicting evidence on hydrogen peroxide s effect on wound healing Some research finds benefit while other research find delays and healing inhibition 103 Its use for home treatment of wounds is generally contraindicated 104 1 5 3 Hydrogen peroxide is used as a desinfectant in dentistry especially in endodotic treatments together with hypochlorite and chlorhexidin and 1 1 5 is also useful for treatment of inflammation of third molars wisdom teeth 105 Use in alternative medicine Edit Practitioners of alternative medicine have advocated the use of hydrogen peroxide for various conditions including emphysema influenza AIDS and in particular cancer 106 There is no evidence of effectiveness and in some cases it has proved fatal 107 108 109 110 111 Both the effectiveness and safety of hydrogen peroxide therapy is scientifically questionable Hydrogen peroxide is produced by the immune system but in a carefully controlled manner Cells called phagocytes engulf pathogens and then use hydrogen peroxide to destroy them The peroxide is toxic to both the cell and the pathogen and so is kept within a special compartment called a phagosome Free hydrogen peroxide will damage any tissue it encounters via oxidative stress a process that also has been proposed as a cause of cancer 112 Claims that hydrogen peroxide therapy increases cellular levels of oxygen have not been supported The quantities administered would be expected to provide very little additional oxygen compared to that available from normal respiration It is also difficult to raise the level of oxygen around cancer cells within a tumour as the blood supply tends to be poor a situation known as tumor hypoxia Large oral doses of hydrogen peroxide at a 3 concentration may cause irritation and blistering to the mouth throat and abdomen as well as abdominal pain vomiting and diarrhea 107 Ingestion of hydrogen peroxide at concentrations of 35 or higher has been implicated as the cause of numerous gas embolism events resulting in hospitalisation In these cases hyperbaric oxygen therapy was used to treat the embolisms 113 Intravenous injection of hydrogen peroxide has been linked to several deaths 109 110 111 The American Cancer Society states that there is no scientific evidence that hydrogen peroxide is a safe effective or useful cancer treatment 108 Furthermore the therapy is not approved by the U S FDA Historical incidents Edit On 16 July 1934 in Kummersdorf Germany a propellant tank containing an experimental monopropellant mixture consisting of hydrogen peroxide and ethanol exploded during a test killing three people 114 During the Second World War doctors in German concentration camps experimented with the use of hydrogen peroxide injections in the killing of human subjects 115 In April 1992 an explosion occurred at the hydrogen peroxide plant at Jarrie in France due to technical failure of the computerised control system and resulting in one fatality and wide destruction of the plant 116 Several people received minor injuries after a hydrogen peroxide spill on board a flight between the U S cities of Orlando and Memphis on 28 October 1998 117 The Russian submarine K 141 Kursk sailed to perform an exercise of firing dummy torpedoes at the Pyotr Velikiy a Kirov class battlecruiser On 12 August 2000 at 11 28 local time 07 28 UTC there was an explosion while preparing to fire the torpedoes The only credible report to date is that this was due to the failure and explosion of one of the Kursk s hydrogen peroxide fueled torpedoes It is believed that HTP a form of highly concentrated hydrogen peroxide used as propellant for the torpedo seeped through its container damaged either by rust or in the loading procedure back on land where an incident involving one of the torpedoes accidentally touching ground went unreported The vessel was lost with all hands A similar incident was responsible for the loss of HMS Sidon in 1955 118 On 15 August 2010 a spill of about 30 US gallons 110 L of cleaning fluid occurred on the 54th floor of 1515 Broadway in Times Square New York City The spill which a spokesperson for the New York City fire department said was of hydrogen peroxide shut down Broadway between West 42nd and West 48th streets as fire engines responded to the hazmat situation There were no reported injuries 119 See also EditFOX reagent used to measure levels of hydrogen peroxide in biological systems Hydrogen chalcogenide Retrobright a process using hydrogen peroxide to restore yellowed Acrylonitrile butadiene styrene plasticReferences EditNotes 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great description of properties amp chemistry of H2O2 March J 1992 Advanced Organic Chemistry 4th ed New York Wiley p 723 Hess WT 1995 Hydrogen Peroxide Kirk Othmer Encyclopedia of Chemical Technology Vol 13 4th ed New York Wiley pp 961 995 External links Edit Wikimedia Commons has media related to Hydrogen peroxide Wikiversity has learning resources about Observing the Effects of Concentration on Enzyme Activity Hydrogen Peroxide at The Periodic Table of Videos University of Nottingham Material Safety Data Sheet ATSDR Agency for Toxic Substances and Disease Registry FAQ International Chemical Safety Card 0164 NIOSH Pocket Guide to Chemical Hazards Process flow sheet of Hydrogen Peroxide Production by anthrahydroquinone autoxidation Hydrogen Peroxide Handbook by Rocketdyne IR spectroscopic study J Phys Chem Retrieved from https en wikipedia org w index php title Hydrogen peroxide amp oldid 1150867242, wikipedia, wiki, book, books, library,

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