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The toxicity of chlorine comes from its oxidizing power. When chlorine is inhaled at concentrations above 30 ppm, it begins to react with water and cells, which change it into [[hydrochloric acid]] (HCl) and [[hypochlorous acid]] (HClO).
The toxicity of chlorine comes from its oxidizing power. When chlorine is inhaled at concentrations above 30 ppm, it begins to react with water and cells, which change it into [[hydrochloric acid]] (HCl) and [[hypochlorous acid]] (HClO).


When used at specified levels for water disinfection, the reaction of chlorine with water is not a major concern for human health. However, other materials present in the water may generate disinfection by-products that can damage human health.<ref>{{cite web|url=http://www.aces.uiuc.edu/news/stories/news4724.html|title=What's in your Water?: Disinfectants Create Toxic By-products|date=2009-03-31|work=ACES News|publisher=College of Agricultural, Consumer and Environmental Sciences – University of Illinois at Urbana-Champaign|accessdate=2009-03-31}}</ref><ref>{{cite journal |doi=10.1016/j.mrrev.2007.09.001 |title=Occurrence, genotoxicity, and carcinogenicity of regulated and emerging disinfection by-products in drinking water: A review and roadmap for research |year=2007 |last1=Richardson |first1=Susan D. |last2=Plewa |first2=Michael J. |last3=Wagner |first3=Elizabeth D. |last4=Schoeny |first4=Rita |last5=DeMarini |first5=David M. |journal=Mutation Research/Reviews in Mutation Research |volume=636 |pages=178–242 |pmid=17980649}}</ref>
When used at specified levels for water disinfection, the reaction of chlorine with water is not a major concern for human health. Other materials present in the water may generate disinfection by-products that are associated with negative effects on human health <ref>{{cite web|url=http://www.aces.uiuc.edu/news/stories/news4724.html|title=What's in your Water?: Disinfectants Create Toxic By-products|date=2009-03-31|work=ACES News|publisher=College of Agricultural, Consumer and Environmental Sciences – University of Illinois at Urbana-Champaign|accessdate=2009-03-31}}</ref><ref>{{cite journal |doi=10.1016/j.mrrev.2007.09.001 |title=Occurrence, genotoxicity, and carcinogenicity of regulated and emerging disinfection by-products in drinking water: A review and roadmap for research |year=2007 |last1=Richardson |first1=Susan D. |last2=Plewa |first2=Michael J. |last3=Wagner |first3=Elizabeth D. |last4=Schoeny |first4=Rita |last5=DeMarini |first5=David M. |journal=Mutation Research/Reviews in Mutation Research |volume=636 |pages=178–242 |pmid=17980649}}</ref>, although the health risk is far lower than drinking undisinfected water.


==See also==
==See also==

Revision as of 05:05, 9 August 2012

This article is about the chemical element. For the bleach, see Sodium hypochlorite. For the film, see Chlorine (film).
Chlorine, 17Cl
A glass container filled with chlorine gas
Chlorine
Pronunciation/ˈklɔːriːn, -aɪn/ ​(KLOR-een, -⁠eyen)
Appearancepale yellow-green gas
Standard atomic weight Ar°(Cl)
Chlorine in the periodic table
Hydrogen Helium
Lithium Beryllium Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium Aluminium Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Caesium Barium Lanthanum Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury (element) Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawrencium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Nihonium Flerovium Moscovium Livermorium Tennessine Oganesson
F
↑
Cl
↓
Br
sulfur ← chlorine → argon
Atomic number (Z)17
Groupgroup 17 (halogens)
Periodperiod 3
Block  p-block
Electron configuration[Ne] 3s2 3p5
Electrons per shell2, 8, 7
Physical properties
Phase at STPgas
Melting point(Cl2) 171.6 K ​(−101.5 °C, ​−150.7 °F)
Boiling point(Cl2) 239.11 K ​(−34.04 °C, ​−29.27 °F)
Density (at STP)3.2 g/L
when liquid (at b.p.)1.5625 g/cm3[3]
Triple point172.22 K, ​1.392 kPa[4]
Critical point416.9 K, 7.991 MPa
Heat of fusion(Cl2) 6.406 kJ/mol
Heat of vaporization(Cl2) 20.41 kJ/mol
Molar heat capacity(Cl2)
33.949 J/(mol·K)
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 128 139 153 170 197 239
Atomic properties
Oxidation statescommon: −1, +1, +3, +5, +7
+2,[5] +4,[5] +6[5]
ElectronegativityPauling scale: 3.16
Ionization energies
  • 1st: 1251.2 kJ/mol
  • 2nd: 2298 kJ/mol
  • 3rd: 3822 kJ/mol
  • (more)
Covalent radius102±4 pm
Van der Waals radius175 pm
Color lines in a spectral range
Spectral lines of chlorine
Other properties
Natural occurrenceprimordial
Crystal structure ​orthorhombic (oS8)
Lattice constants
Orthorhombic crystal structure for chlorine
a = 630.80 pm
b = 455.83 pm
c = 815.49 pm (at triple point)[6]
Thermal conductivity8.9×10−3 W/(m⋅K)
Electrical resistivity>10 Ω⋅m (at 20 °C)
Magnetic orderingdiamagnetic[7]
Molar magnetic susceptibility−40.5×10−6 cm3/mol[8]
Speed of sound206 m/s (gas, at 0 °C)
CAS NumberCl2: 7782-50-5
History
Discovery and first isolationCarl Wilhelm Scheele (1774)
Recognized as an element byHumphry Davy (1808)
Isotopes of chlorine
Main isotopes[9] Decay
abun­dance half-life (t1/2) mode pro­duct
35Cl 76% stable
36Cl trace 3.01×105 y β− 36Ar
ε 36S
37Cl 24% stable
 Category: Chlorine
| references

Chlorine (/[invalid input: 'icon']ˈklɔːriːn/ KLOHR-een; from Template:Lang-grc) is a chemical element with symbol Cl and atomic number 17. It is the second lightest halogen after fluorine. Chlorine is in the halogen group (17). The element forms diatomic molecules under standard conditions, called dichlorine. It has the highest electron affinity and the third highest electronegativity of all the elements; for this reason, chlorine is a strong oxidizing agent.

The most common compound of chlorine, sodium chloride, has been known since ancient times; however, around 1630, chlorine gas was obtained by the Belgian chemist and physician Jan Baptist van Helmont. The synthesis and characterization of elemental chlorine occurred in 1774 by Swedish chemist Carl Wilhelm Scheele, who called it "dephlogisticated muriatic acid air," having thought he synthesized the oxide obtained from the hydrochloric acid. Because acids were thought at the time to necessarily contain oxygen, a number of chemists, including Claude Berthollet, suggested that Scheele's dephlogisticated muriatic acid air must be a combination of oxygen and the yet undiscovered element, and Scheele named the supposed new element within this oxide as muriaticum. The suggestion that this newly discovered gas was a simple element was made in 1809 by Joseph Louis Gay-Lussac and Louis-Jacques. This was confirmed by Sir Humphry Davy in 1810, who named it chlorine, from the Greek word χλωρος (chlōros), meaning "green-yellow."

Chlorine is a component of various compounds, including table salt. It is the second most abundant halogen and 21st most abundant chemical element in Earth's crust. The great oxidizing potential of chlorine led it to its bleaching and disinfectant uses, as well as uses of an essential reagent in the chemical industry. As a common disinfectant, chlorine compounds are used in swimming pools to keep them clean and sanitary. In the upper atmosphere, chlorine-containing molecules such as chlorofluorocarbons have been implicated in ozone depletion. Elemental chlorine is extremely dangerous and poisonous for all lifeforms; however, chlorine is necessary to most forms of life, including humans, in form of chloride ions.

Characteristics

Physical characteristics

Chlorine, liquified under a pressure of 7.4 bar at room temperature, displayed in a quartz ampule embedded in acrylic glass.

At standard temperature and pressure, two chlorine atoms form the diatomic molecule Cl2.[10] This is a yellow-green gas that has a distinctive strong odor, familiar to most from common household bleach.[11] The bonding between the two atoms is relatively weak (only 242.580 ± 0.004 kJ/mol), which makes the Cl2 molecule highly reactive. The boiling point at regular atmosphere is around −34 ˚C, but it can be liquefied at room temperature with pressures above 740 kPa.[12]

Chemical characteristics

Along with fluorine, bromine, iodine, and astatine, chlorine is a member of the halogen series that forms the group 17 (formerly VII, VIIA, or VIIB) of the periodic table. Chlorine forms compounds with almost all of the elements to give compounds that are usually called chlorides. Chlorine gas reacts with most organic compounds, and will even sluggishly support the combustion of hydrocarbons.[13]

Hydrolysis

At 25 °C and atmospheric pressure, one liter of water dissolves 3.26 g or 1.125 L of gaseous chlorine.[14] Solutions of chlorine in water contain chlorine (Cl2), hydrochloric acid, and hypochlorous acid:

Cl2 + H2O ⇌ HCl + HClO

This conversion to the right is called disproportionation, because the ingredient chlorine both increases and decreases in formal oxidation state. The solubility of chlorine in water is increased if the water contains dissolved alkali hydroxide, and in this way, chlorine bleach is produced.[15]

Cl2 + 2 OH– → ClO– + Cl– + H2O

Chlorine gas only exists in a neutral or acidic solution.

Compounds

See also: Category:Chlorine compounds

Chlorine exists in all odd numbered oxidation states from −1 to +7, as well as the elemental state of zero and four in chlorine dioxide (see table below, and also structures in chlorite).[16] Progressing through the states, hydrochloric acid can be oxidized using manganese dioxide, or hydrogen chloride gas oxidized catalytically by air to form elemental chlorine gas.[17]

Oxidation
state		 Name Formula Characteristic compounds
−1 chlorides Cl− ionic chlorides, organic chlorides, hydrochloric acid
0 chlorine Cl2 elemental chlorine
+1 hypochlorites ClO− sodium hypochlorite, calcium hypochlorite
+2 Organoaluminium compounds -Cl-Al Ethylaluminium sesquichloride
+3 chlorites ClO−
2		 sodium chlorite
+4 chlorine(IV) ClO
2		 chlorine dioxide
+5 chlorates ClO−
3		 sodium chlorate, potassium chlorate, chloric acid
+7 perchlorates ClO−
4		 perchloric acid, perchlorate salts such as magnesium perchlorate, dichlorine heptoxide
Chlorine oxides

Chlorine forms a variety of oxides, as seen above: chlorine dioxide (ClO2), dichlorine monoxide (Cl2O), dichlorine hexoxide (Cl2O6), dichlorine heptoxide (Cl2O7). The anionic derivatives of these same oxides are also well known including chlorate (ClO−
3), chlorite (ClO−
2), hypochlorite (ClO−), and perchlorate (ClO−
4). The acid derivatives of these anions are hypochlorous acid (HOCl), chloric acid (HClO3) and perchloric acid (HClO4). The chloroxy cation chloryl (ClO2+) is known and has the same structure as chlorite but with a positive charge and chlorine in the +5 oxidation state.[18] The compound "chlorine trioxide", rather than being the expected +6 oxidation state, is instead a mixture of +5 and +7 states, occurring as the ionic compound chloryl perchlorate, [ClO
2]+
[ClO
4]−
 commonly called dichlorine hexoxide.[19]

In hot concentrated alkali solution hypochlorite disproportionates:

2 ClO− → Cl− + ClO−
2
ClO− + ClO−
2 → Cl− + ClO−
3

Sodium chlorate and potassium chlorate can be crystallized from solutions formed by the above reactions. If their crystals are heated, they undergo a further, final disproportionation:

4 ClO−
3 → Cl− + 3 ClO−
4

This same progression from chloride to perchlorate can be accomplished by electrolysis. The anode reaction progression is:[20]

Reaction Electrode
potential
Cl− + 2 OH− → ClO− + H2O + 2 e− +0.89 volts
ClO− + 2 OH− → ClO−
2 + H2O + 2 e−		 +0.67 volts
ClO−
2 + 2 OH− → ClO−
3 + H2O + 2 e−		 +0.33 volts
ClO−
3 + 2 OH− → ClO−
4 + H2O + 2 e−		 +0.35 volts

Each step is accompanied at the cathode by

2 H2O + 2 e− → 2 OH− + H2 (−0.83 volts)
Interhalogen compounds

Chlorine oxidizes bromide and iodide salts to bromine and iodine, respectively. However, it cannot oxidize fluoride salts to fluorine. It makes a variety of interhalogen compounds such as the chlorine fluorides, chlorine monofluoride (ClF), chlorine trifluoride (ClF3), chlorine pentafluoride (ClF5). Chlorides of bromine and iodine are also known.[21]

Organochlorine compounds
Main article: Organochloride

Chlorine is used extensively in organic chemistry in substitution and addition reactions. Chlorine often imparts many desired properties to an organic compound, in part owing to its electronegativity. Some organochlorine compounds are also serious pollutants, either as side products of industrial processes or as persistent pesticides.

Many important industrial products are produced via organochlorine intermediates. Examples include polycarbonates, polyurethanes, silicones, polytetrafluoroethylene, carboxymethyl cellulose, and propylene oxide. Like the other halogens, chlorine participates in free-radical substitution reactions with hydrogen-containing organic compounds. When applied to organic substrates, reaction is often—but not invariably—non-regioselective, and, hence, may result in a mixture of isomeric products. It is often difficult to control the degree of substitution as well, so multiple substitutions are common. If the different reaction products are easily separated, e.g., by distillation, substitutive free-radical chlorination (in some cases accompanied by concurrent thermal dehydrochlorination) may be a useful synthetic route. Industrial examples of this are the production of methyl chloride, methylene chloride, chloroform, and carbon tetrachloride from methane, allyl chloride from propylene, and trichloroethylene, and tetrachloroethylene from 1,2-dichloroethane.

Like the other halides, chlorine undergoes electrophilic addition reactions, the most notable one being the chlorination of alkenes and aromatic compounds with a Lewis acid catalyst. Organic chlorine compounds tend to be less reactive in nucleophilic substitution reactions than the corresponding bromine or iodine derivatives, but they tend to be cheaper. They may be activated for reaction by substituting with a tosylate group, or by the use of a catalytic amount of sodium iodide.[citation needed]

Chlorides
Main article: Chloride

Chlorine combines with almost all elements to give chlorides. Compounds with oxygen, nitrogen, xenon, and krypton are known, but do not form by direct reaction of the elements.[22] Chloride is one of the most common anions in nature. Hydrogen chloride and its aqueous solution, hydrochloric acid, are produced on megaton scale annually both as valued intermediates but sometimes as undesirable pollutants.

Occurrence

See also: Category:Halide minerals

In nature, chlorine is found primarily as the chloride ion, a component of the salt that is deposited in the earth or dissolved in the oceans — about 1.9% of the mass of seawater is chloride ions. Even higher concentrations of chloride are found in the Dead Sea and in underground brine deposits. Most chloride salts are soluble in water, thus, chloride-containing minerals are usually only found in abundance in dry climates or deep underground. In the Earth's crust, chlorine is present at average concentrations of about 126 parts per million,[23] predominantly in such minerals as halite (sodium chloride), sylvite (potassium chloride), and carnallite (potassium magnesium chloride hexahydrate). Over 2000 naturally occurring organic chlorine compounds are known.[24]

In the interstellar medium, chlorine is produced in supernovae via the r-process.[25]

Isotopes

Main article: Isotopes of chlorine

Chlorine has a wide range of isotopes. The two stable isotopes are 35Cl (75.77%) and 37Cl (24.23%).[26] Together they give chlorine an atomic weight of 35.4527 g/mol. The half-integer value for chlorine's weight caused some confusion in the early days of chemistry, when it had been postulated that atoms were composed of even units of hydrogen (see Proust's law), and the existence of chemical isotopes was unsuspected.[27]

Trace amounts of radioactive 36Cl exist in the environment, in a ratio of about 7x10−13 to 1 with stable isotopes. 36Cl is produced in the atmosphere by spallation of 36Ar by interactions with cosmic ray protons. In the subsurface environment, 36Cl is generated primarily as a result of neutron capture by 35Cl or muon capture by 40Ca. 36Cl decays to 36S and to 36Ar, with a combined half-life of 308,000 years. The half-life of this hydrophilic nonreactive isotope makes it suitable for geologic dating in the range of 60,000 to 1 million years. Additionally, large amounts of 36Cl were produced by irradiation of seawater during atmospheric detonations of nuclear weapons between 1952 and 1958. The residence time of 36Cl in the atmosphere is about 1 week. Thus, as an event marker of 1950s water in soil and ground water, 36Cl is also useful for dating waters less than 50 years before the present. 36Cl has seen use in other areas of the geological sciences, including dating ice and sediments.[26]

History

The most common compound of chlorine, sodium chloride, has been known since ancient times; archaeologists have found evidence that rock salt was used as early as 3000 BC and brine as early as 6000 BC.[28] Around 1630, chlorine was recognized as a gas by the Belgian chemist and physician Jan Baptist van Helmont.[29]

Carl Wilhelm Scheele

Elemental chlorine was first prepared and studied in 1774 by Swedish chemist Carl Wilhelm Scheele, and, therefore, he is credited for its discovery.[30] He called it "dephlogisticated muriatic acid air" since it is a gas (then called "airs") and it came from hydrochloric acid (then known as "muriatic acid").[30] However, he failed to establish chlorine as an element, mistakenly thinking that it was the oxide obtained from the hydrochloric acid (see phlogiston theory).[30] He named the new element within this oxide as muriaticum.[30] Regardless of what he thought, Scheele did isolate chlorine by reacting MnO2 (as the mineral pyrolusite) with HCl:[29]

4 HCl + MnO2 → MnCl2 + 2 H2O + Cl2

Scheele observed several of the properties of chlorine: the bleaching effect on litmus, the deadly effect on insects, the yellow green color, and the smell similar to aqua regia.[31]

At the time, common chemical theory was: any acid is a compound that contains oxygen (still sounding in the German and Dutch names of oxygen: sauerstoff or zuurstof, both translating into English as acid stuff), so a number of chemists, including Claude Berthollet, suggested that Scheele's dephlogisticated muriatic acid air must be a combination of oxygen and the yet undiscovered element, muriaticum.[32][33][34]

In 1809, Joseph Louis Gay-Lussac and Louis-Jacques Thénard tried to decompose dephlogisticated muriatic acid air by reacting it with charcoal to release the free element muriaticum (and carbon dioxide).[30] They did not succeed and published a report in which they considered the possibility that dephlogisticated muriatic acid air is an element, but were not convinced.[35]

In 1810, Sir Humphry Davy tried the same experiment again, and concluded that it is an element, and not a compound.[30] He named this new element as chlorine, from the Greek word χλωρος (chlōros), meaning green-yellow.[36] The name halogen, meaning salt producer, was originally defined for chlorine in 1811 by Johann Salomo Christoph Schweigger; the term was applied to the rest of the elements in this family after suggestion by Jöns Jakob Berzelius in 1842.[37][38] In 1823, Michael Faraday liquefied chlorine for the first time,[39][40] and demonstrated that what was then known as "solid chlorine" had a structure of chlorine hydrate (Cl2·H2O).[29]

Chlorine gas was first used by French chemist Claude Berthollet to bleach textiles in 1785.[41][42] Modern bleaches resulted from further work by Berthollet, who first produced sodium hypochlorite in 1789 in his laboratory on the quay Javel in Paris, France, by passing chlorine gas through a solution of sodium carbonate. The resulting liquid, known as "Eau de Javel" ("Javel water"), was a weak solution of sodium hypochlorite. However, this process was not very efficient, and alternative production methods were sought. Scottish chemist and industrialist Charles Tennant first produced a solution of calcium hypochlorite ("chlorinated lime"), then solid calcium hypochlorite (bleaching powder).[41] These compounds produced low levels of elemental chlorine, and could be more efficiently transported than sodium hypochlorite, which remained as dilute solutions because when purified to eliminate water, it became a dangerously powerful and unstable oxidizer. Near the end of the nineteenth century, E. S. Smith patented a method of sodium hypochlorite production involving electrolysis of brine to produce sodium hydroxide and chlorine gas, which then mixed to form sodium hypochlorite.[43] This is known as the chloralkali process, first introduced on an industrial scale in 1892, and now the source of essentially all modern elemental chlorine, sodium hydroxide, and sodium hypochlorite production.

Elemental chlorine solutions dissolved in chemically basic water (sodium and calcium hypochlorite) was first used as anti-putrification agents and disinfectants in the 1820s, in France, long before the establishment of the germ theory of disease. This work is mainly due to Antoine-Germain Labarraque, who adapted Berthollet's "Javel water" bleach and other chlorine preparations for the purpose (see a more complete history, see below). Elemental chlorine has since served a continuous function in topical antisepsis (wound irrigation solutions and the like) as well as public sanitation (especially of swimming and drinking water).

In 1826, silver chloride was used to produce photographic images for the first time.[44] Chloroform was first used as an anesthetic in 1847.[44]

Polyvinyl chloride (PVC) was invented in 1912, initially without a purpose.[44]

Chlorine gas was first introduced as a weapon on April 22, 1915, at Ypres by the German Army,[45][46] and the results of this weapon were disastrous because gas masks had not been mass distributed and were tricky to get on quickly.

Production

Liquid chlorine analysis
Main articles: Chlorine production and Chloralkali process

In industry, elemental chlorine is usually produced by the electrolysis of sodium chloride dissolved in water. This method, the chloralkali process industrialized in 1892, now provides essentially all industrial chlorine gas.[47] Along with chlorine, the method yields hydrogen gas and sodium hydroxide (the latter actually being the most crucial of the three industrial products produced by the process). The process proceeds according to the following chemical equation:[17]

2 NaCl + 2 H2O → Cl2 + H2 + 2 NaOH

The electrolysis of chloride solutions all proceed according to the following equations:

Cathode: 2 H+ (aq) + 2 e− → H2 (g)
Anode: 2 Cl− (aq) → Cl2 (g) + 2 e−

Overall process: 2 NaCl (or KCl) + 2 H2O → Cl2 + H2 + 2 NaOH (or KOH) In diaphragm cell electrolysis, an asbestos (or polymer-fiber) diaphragm separates a cathode and an anode, preventing the chlorine forming at the anode from re-mixing with the sodium hydroxide and the hydrogen formed at the cathode.[48] The salt solution (brine) is continuously fed to the anode compartment and flows through the diaphragm to the cathode compartment, where the caustic alkali is produced and the brine is partially depleted. Diaphragm methods produce dilute and slightly impure alkali but they are not burdened with the problem of preventing mercury discharge into the environment and they are more energy efficient. Membrane cell electrolysis employ permeable membrane as an ion exchanger. Saturated sodium (or potassium) chloride solution is passed through the anode compartment, leaving at a lower concentration.[49] This method is more efficient than the diaphragm cell and produces very pure sodium (or potassium) hydroxide at about 32% concentration, but requires very pure brine.

Membrane cell process for chloralkali production

Laboratory methods

Small amounts of chlorine gas can be made in the laboratory by combining hydrochloric acid and manganese dioxide. Alternatively a strong acid such as sulfuric acid or hydrochloric acid reacts with sodium hypochlorite solution to release chlorine gas but reacts with sodium chlorate to produce chlorine gas and chlorine dioxide gas as well. In the home, accidents occur when hypochlorite bleach solutions are combined with certain acidic drain-cleaners.

Applications

Production of industrial and consumer products

Principal applications of chlorine are in the production of a wide range of industrial and consumer products.[50][51] For example, it is used in making plastics, solvents for dry cleaning and metal degreasing, textiles, agrochemicals and pharmaceuticals, insecticides, dyestuffs, household cleaning products, etc. Quantitatively, about 63% and 18% of all chlorine are used in the manufacture of organic and inorganic chlorine compounds, respectively,[47] and about 15,000 chlorine compounds are being used commercially.[31] The remaining 19% is used for bleaches and disinfection products.[47] The most significant of organic compounds in terms of production volume are 1,2-dichloroethane and vinyl chloride, intermediates in the production of PVC. Other particularly important organochlorines are methyl chloride, methylene chloride, chloroform, vinylidene chloride, trichloroethylene, perchloroethylene, allyl chloride, epichlorohydrin, chlorobenzene, dichlorobenzenes, and trichlorobenzenes. The major inorganic compounds include HCl, Cl2O, HOCl, NaClO3, chlorinated isocyanurates, AlCl3, SiCl4, SnCl4, PCl3, PCl5, POCl3, AsCl3, SbCl3, SbCl5, BiCl3, S2Cl2, SCl2, SOCI2, CIF3, ICl, ICl3, TiCl3, TiCl4, MoCl5, FeCl3, ZnCl2, etc.[47][52]

Public sanitation, disinfection, and antisepsis

Main articles: Chlorination, Bleach, and Antoine Labarraque

Putrifaction

Portrait of Labarraque

In France (as elsewhere) there was a need to process animal guts in order to make musical instrument strings, Goldbeater's skin and other products. This was carried out "gut factories" as an odiferous and unhealthy business. In or about 1820,[53] a prize for the discovery of a method, chemical or mechanical, that could be used to separate the peritoneal membrane of animal intestines without causing putrefaction, was offered.[54][55] It was won by Antoine-Germain Labarraque, a 44 year-old French chemist and pharmacist who had discovered that Berthollet's chlorinated bleaching solutions ("Eau de Javel") not only destroyed the smell of putrifaction of animal tissue decomposition, but also retarded the decomposition process itself.[55][56]

Labarraque's research resulted in chlorides and hypochlorites of lime (calcium hypochlorite) and of sodium (sodium hypochlorite) being employed not only in the boyauderies but also for the routine disinfection and deodorisation of latrines, sewers, markets, abattoirs, anatomical theatres and morgues.[57] They were also used, with success, in hospitals, lazarets, prisons, infirmaries (both on land and at sea), magnaneries, stables, cattle-sheds, etc.; and for exhumations,[58] embalming, during outbreaks of epidemic illness, fever, Blackleg (disease) in cattle, etc.[54]

Against infection and contagion

Labarraque's chlorinated lime and soda solutions had been advocated in 1828 to prevent infection (called "contagious infection", and presumed to be transmitted by "miasmas") and also to treat putrefaction of existing wounds, including septic wounds.[59] In this 1828 work, Labarraque recommended for the doctor to breathe chlorine, wash his hands with chlorinated lime, and even sprinkle chlorinated lime about the patient's bed, in cases of "contagious infection." In 1828, it was well known that some infections would contagious, even though the agency of the microbe was not to be realized or discovered for more than half a century.

During the Paris cholera outbreak of 1832, large quantities of so-called chloride of lime were used to disinfect the capital. This was not simply modern calcium chloride, but contained chlorine gas dissolved in lime-water (dilute calcium hydroxide) to form calcium hypochlorite (chlorinated lime). Labarraque's discovery helped to remove the terrible stench of decay from hospitals and dissecting rooms, and, by doing so, effectively deodorised the Latin Quarter of Paris.[60] These "putrid miasmas" were thought by many to be responsible for the spread of "contagion" and "infection"- both words used before the germ theory of infection. In 1850, chlorine in lime-water was used by John Snow to purify the water supply in London after an outbreak of cholera. Both uses preceded the germ theory of disease, and were based on destruction of odors and "putrid matter."

Semmelweis and experiments with antisepsis

Portrait of Semmelweis

Perhaps the most famous application of Labarraque's chlorine and chemical base solutions was in 1847, when Ignaz Semmelweis used (first) chlorine-water (simply chlorine dissolved in pure water), then cheaper chlorinated lime solutions, to deodorize the hands of Austrian doctors, which Semmelweis noticed still carried the stench of decomposition from the dissection rooms to the patient examination rooms. Semmelweis, still long before the germ theory of disease, had theorized that "cadaveric particles" were somehow transmitting decay from fresh medical cadavers to living patients, and he used the well-known "Labarraque's solutions" as the only known method to remove the smell of decay and tissue decomposition (which he found that soap did not). The solutions proved to be far more effective germicide antiseptics than soap (Semmelweis was also aware of their greater efficacy, but not the reason), and this resulted in Semmelweis's (later) celebrated success in stopping the transmission of childbed fever ("puerperal fever") in the maternity wards of Vienna General Hospital in Austria in 1847.[61]

Much later, during World War I in 1916, a standardized and diluted modification of Labarraque's solution containing hypochlorite and boric acid was developed by Henry Drysdale Dakin. Called Dakin's solution, the method of wound irrigation with chlorinated solutions allowed antiseptic treatment of a wide variety of open wounds, long before the modern antibiotic era. A modified version of this solution continues to be employed in wound irrigation in the modern era, where it remains effective against multiply-antibiotic resistant bacteria (see Century Pharmaceuticals).

Public sanitation

By 1918, the US Department of Treasury called for all drinking water to be disinfected with chlorine. Chlorine is presently an important chemical for water purification (such as water treatment plants), in disinfectants, and in bleach. Chlorine in water is more than three times as effective as a disinfectant against Escherichia coli than an equivalent concentration of bromine, and is more than six times more effective than an equivalent concentration of iodine.[62]

Chlorine is usually used (in the form of hypochlorous acid) to kill bacteria and other microbes in drinking water supplies and public swimming pools. In most private swimming pools, chlorine itself is not used, but rather sodium hypochlorite, formed from chlorine and sodium hydroxide, or solid tablets of chlorinated isocyanurates. The drawback of using chlorine in swimming pools is that the chlorine reacts with a human's hair and skin because hair and skin are made from protein.(Reaction with protein amino groups) Even small water supplies are now routinely chlorinated.[13]

It is often impractical to store and use poisonous chlorine gas for water treatment, so alternative methods of adding chlorine are used. These include hypochlorite solutions, which gradually release chlorine into the water, and compounds like sodium dichloro-s-triazinetrione (dihydrate or anhydrous), sometimes referred to as "dichlor", and trichloro-s-triazinetrione, sometimes referred to as "trichlor". These compounds are stable while solid and may be used in powdered, granular, or tablet form. When added in small amounts to pool water or industrial water systems, the chlorine atoms hydrolyze from the rest of the molecule forming hypochlorous acid (HOCl), which acts as a general biocide, killing germs, micro-organisms, algae, and so on.[63][64]

Use as a weapon

World War I

Main article: Poison gas in World War I

Chlorine gas, also known as bertholite, was first used as a weapon in World War I by Germany on April 22, 1915 in the Second Battle of Ypres.[65] As described by the soldiers it had a distinctive smell of a mixture between pepper and pineapple. It also tasted metallic and stung the back of the throat and chest. Chlorine can react with water in the mucosa of the lungs to form hydrochloric acid, an irritant that can be lethal. The damage done by chlorine gas can be prevented by a gas mask, or other filtration method, which makes the overall chance of death by chlorine gas much lower than those of other chemical weapons. It was pioneered by a German scientist later to be a Nobel laureate, Fritz Haber of the Kaiser Wilhelm Institute in Berlin, in collaboration with the German chemical conglomerate IG Farben, who developed methods for discharging chlorine gas against an entrenched enemy. It is alleged that Haber's role in the use of chlorine as a deadly weapon drove his wife, Clara Immerwahr, to suicide.[66] After its first use, chlorine was utilized by both sides as a chemical weapon, but it was soon replaced by the more deadly phosgene and mustard gas.[67]

Iraq War

Main article: 2007 chlorine bombings in Iraq
Chlorine "attack" on an acetal resin plumbing joint.

Chlorine gas has also been used by insurgents against the local population and coalition forces in the Iraq War in the form of chlorine bombs. On March 17, 2007, for example, three chlorine filled trucks were detonated in the Anbar province killing two and sickening over 350.[68] Other chlorine bomb attacks resulted in higher death tolls, with more than 30 deaths on two separate occasions.[69] Most of the deaths were caused by the force of the explosions rather than the effects of chlorine, since the toxic gas is readily dispersed and diluted in the atmosphere by the blast. The Iraqi authorities have tightened up security for chlorine, which is essential for providing safe drinking water for the population.

Chlorine cracking

The element is widely used for purifying water owing to its powerful oxidizing properties, especially potable water supplies and water used in swimming pools. Several catastrophic collapses of swimming pool ceilings have occurred owing to stress corrosion cracking of stainless steel rods used to suspend them.[70] Some polymers are also sensitive to attack, including acetal resin and polybutene. Both materials were used in hot and cold water domestic supplies, and stress corrosion cracking caused widespread failures in the USA in the 1980s and 1990s. One example shows an acetal joint in a water supply system, which, when it fractured, caused substantial physical damage to computers in the labs below the supply. The cracks started at injection molding defects in the joint and grew slowly until finally triggered. The fracture surface shows iron and calcium salts that were deposited in the leaking joint from the water supply before failure.[71]

Health effects

NFPA 704
NFPA 704
safety square
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
3
0
0

Chlorine is a toxic gas that irritates the respiratory system. Because it is heavier than air, it tends to accumulate at the bottom of poorly ventilated spaces. Chlorine gas is a strong oxidizer, which may react with flammable materials.[72]

Chlorine is detectable with measuring devices in concentrations of as low as 0.2 parts per million (ppm), and by smell at 3 ppm. Coughing and vomiting may occur at 30 ppm and lung damage at 60 ppm. About 1000 ppm can be fatal after a few deep breaths of the gas.[31] Breathing lower concentrations can aggravate the respiratory system, and exposure to the gas can irritate the eyes.[73] The toxicity of chlorine comes from its oxidizing power. When chlorine is inhaled at concentrations above 30 ppm, it begins to react with water and cells, which change it into hydrochloric acid (HCl) and hypochlorous acid (HClO).

When used at specified levels for water disinfection, the reaction of chlorine with water is not a major concern for human health. Other materials present in the water may generate disinfection by-products that are associated with negative effects on human health [74][75], although the health risk is far lower than drinking undisinfected water.

See also

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