Chlorine

History

Chlorine was discovered in 1774 by Swedish chemist Sir Humphry Davy, who insisted that it was in fact an element.

World War I

Main article: Poison gas in World War I

Chlorine gas, also known as bertholite, was first mustard gas.^[2]

Iraq War

Main article: 2007 chlorine bombings in Iraq

Chlorine gas has also been used by insurgents in the Iraq War as a chemical weapon to terrorize the local population and coalition forces. On March 17, 2007, for example, three chlorine filled trucks were detonated in the Anbar province killing 2 and sickening over 350.^[3] Other chlorine bomb attacks resulted in higher death tolls, with more than 30 deaths on two separate occasions.^[4] 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.

Isotopes

Main article: Isotopes of chlorine

Chlorine has isotopes with atoms in bulk an apparent atomic weight of 35.5 g/mol.

³⁶Cl

Trace amounts 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.

Notable characteristics

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  Chlorine gas is C and atmospheric pressure, one liter of water dissolves 3.10 L of gaseous chlorine, and at 30°C, 1 L of water dissolves only 1.77 liters of chlorine.^[5]

This element is a member of the electrolysis. As the chloride ion, Cl⁻, it is also the most abundant dissolved ion in ocean water.

Occurrence

See also Halide minerals.

In nature, chlorine is found primarily as the chloride ion, a component of the carnallite (potassium magnesium chloride hexahydrate). Over 2000 naturally-occurring organic chlorine compounds are known.^[8]

Industrially, elemental chlorine is usually produced by the chemical equation:

2 NaOH

Production

Chlorine gas extraction

Chlorine can be manufactured by potassium chloride, in which case the co-products are hydrogen and caustic potash (potassium hydroxide). There are three industrial methods for the extraction of chlorine by electrolysis of chloride solutions, all proceeding 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)

Mercury cell electrolysis

graphite ones) are placed in a sodium (or potassium) chloride solution flowing over a liquid mercury cathode. When a potential difference is applied and current flows, chlorine is released at the titanium anode and sodium (or potassium) dissolves in the mercury cathode forming an amalgam. This flows continuously into a separate reactor ("denuder" or "secondary cell"), where it is usually converted back to mercury by reaction with water, producing hydrogen and sodium (or potassium) hydroxide at a commercially useful concentration (50% by weight). The mercury is then recycled to the primary cell.

The mercury process is the least energy-efficient of the three main technologies (mercury, diaphragm and membrane) and there are also concerns about mercury emissions.

It is estimated that there are still around 100 mercury-cell plants operating worldwide. In Japan, mercury-based chloralkali production was virtually phased out by 1987 (except for the last two potassium chloride units shut down in 2003). In the United States, there will be only five mercury plants remaining in operation by the end of 2008. In Europe, mercury cells accounted for 43% of capacity in 2006 and Western European producers have committed to closing or converting all remaining chloralkali mercury plants by 2020.^[12]

Diaphragm cell electrolysis

In diaphragm cell electrolysis, an asbestos (or polymer-fiber) diaphragm separates cathode and anode, preventing the chlorine forming at the anode from re-mixing with the sodium hydroxide and the hydrogen formed at the cathode.^[13] This technology was also developed at the end of the nineteenth century. There are several variants of this process: the Le Sueur cell (1893), the Hargreaves-Bird cell (1901), the Gibbs cell (1908), and the Townsend cell (1904).^[14][15] The cells vary in construction and placement of the diaphragm, with some having the diaphragm in direct contact with the cathode.

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 partially depleted.

As a result, diaphragm methods produce alkali that is quite dilute (about 12%) and of lower purity than do mercury cell methods. But diaphragm cells are not burdened with the problem of preventing mercury discharge into the environment. They also operate at a lower voltage, resulting in an energy savings over the mercury cell method^[15], but large amounts of steam are required if the caustic has to be evaporated to the commercial concentration of 50%.

Membrane cell electrolysis

Development of this technology began in the 1970s. The electrolysis cell is divided into two "rooms" by a cation permeable membrane acting as an ion exchanger. Saturated sodium (or potassium) chloride solution is passed through the anode compartment, leaving at a lower concentration.^[16] Sodium (or potassium) hydroxide solution is circulated through the cathode compartment, exiting at a higher concentration. A portion of the concentrated sodium hydroxide solution leaving the cell is diverted as product, while the remainder is diluted with deionized water and passed through the electrolyzer again.

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.

Other electrolytic processes

Although a much lower production scale is involved, electrolytic diaphragm and membrane technologies are also used industrially to recover chlorine from hydrochloric acids solutions, producing hydrogen (but no caustic alkali) as a co-product.

Furthermore, electrolysis of fused chloride salts (magnesium.

Other methods

Before electrolytic methods were used for chlorine production, the direct oxidation of hydrogen chloride with oxygen or air was exercised in the Deacon process:

4 HCl + O₂ → 2 Cl₂ + 2 H₂O

This reaction is accomplished with the use of CuCl₂ as a catalyst and is performed at high temperarature (about 400°C). The amount of extracted chlorine is approximately 80%. Due to the extremely corrosive reaction mixture, industrial use of this method is difficult and several pilot trials failed in the past. Nevertheless, recent developments are promising.

Another earlier process to produce chlorine was to heat brine with acid and manganese dioxide.

2 NaCl + 2H₂SO₄ + MnO₂ → Na₂SO₄ + MnSO₄ + 2 H₂O + Cl₂

Using this process, chemist Weldon process.^[17]

Small amounts of chlorine gas can be made in the laboratory by putting concentrated Manganese dioxide is then added and the flask stoppered. The reaction is not greatly exothermic. As chlorine is denser than air, it can be easily collected by placing the tube inside a flask where it will displace the air. Once full, the collecting flask can be stoppered.

In the laboratory, small amounts of chlorine gas can also be created by adding concentrated sodium chlorate solution.

Industrial production

Large-scale production of chlorine involves several steps and many pieces of equipment. The description below is typical of a membrane plant. The plant also produces simultaneously hydrogen handling.

Brine

Key to the production of chlorine is the operation of the brine saturation/treatment system. Maintaining a properly saturated solution with the correct purity is vital, especially for membrane cells. Many plants have a salt pile which is sprayed with recycled brine. Others have slurry tanks that are fed raw salt.

The raw brine is partially or totally treated with magnesium and other impurities. The brine proceeds to a large clarifier or a filter where the impurities are removed. The total brine is additionally filtered before entering ion exchangers to further remove impurities. At several points in this process, the brine is tested for hardness and strength.

After the ion exchangers the brine is considered pure, and is transferred to storage tanks to be pumped into the cell room. Brine fed to the cell line is heated to the correct temperature to control exit brine temperatures according to the electrical load. Brine exiting the cell room must be treated to remove residual chlorine and control pH before being returned to the saturation stage. This can be accomplished via dechlorination towers with acid and sodium bisulfite addition. Failure to remove chlorine can result in damage to the cells. Brine should be monitored for accumulation of chlorate and sulfate and either have treatment systems in place or purging of the brine loop to maintain safe levels, since chlorate can diffuse through the membranes and contaminate the caustic, while sulfate can damage the anode surface coating.

Cell room

The building that houses the many electrolytic cells is usually called a cell room or cell house, although some plants are built outdoors. This building contains support structures for the cells, connections for supplying electrical power to the cells and piping for the fluids. Monitoring and control of the temperatures of the feed caustic and brine is done to control exit temperatures. Also monitored are the voltages of each cell which vary with the electrical load on the cell room that is used to control the rate of production. Monitoring and control of the pressures in the chlorine and hydrogen headers is also done via pressure control valves.

Direct electrical current is supplied via rectifiers. Plant load is controlled by varying the current to the cells. As the current is increased flow rates for brine, caustic and deionized water are increased while lowering the feed temperatures.

Cooling and drying

Chlorine gas exiting the cell line must be cooled and dried since the exit gas can be over 80º C and contains moisture that allows chlorine gas to be corrosive to iron piping. Cooling the gas allows for a large amount of moisture from the brine to condense out of the gas stream. Cooling also improves the efficiency of the compression and liquefaction stage that follows. Chlorine exiting is ideally between 18º C and 25º C. After cooling the gas stream passes through a series of towers with counter flowing sulfuric acid. These towers progressively remove any remaining moisture from the chlorine gas. After exiting the drying towers the chlorine is filtered to remove any sulfuric acid droplets.

Compression and liquefaction

Several methods of compression may be used: ethylene dichloride (by reaction with ethylene).

Storage and loading

Liquid chlorine is typically gravity-fed to storage tanks. It can be loaded into rail or road tankers via pumps or padded with compressed dry gas.

Caustic handling, evaporation, storage and loading

Caustic fed to the cell room flows in a loop that is simultaneously bled off to storage with a part diluted with deionized water and returned to the cell line for strengthening within the cells. The caustic exiting the cell line must be monitored for strength, to maintain safe concentrations. Too strong or too weak a solution may damage the membranes. Membrane cells typically produce caustic in the range of 30% to 33% by weight. The feed caustic flow is heated at low electrical loads to control its exit temperature. Higher loads require the caustic to be cooled, to maintain correct exit temperatures. The caustic exiting to storage is pulled from a storage tank and may be diluted for sale to customers who require weak caustic or for use on site. Another stream may be pumped into a multiple effect evaporator set to produce commercial 50% caustic. Rail cars and tanker trucks are loaded at loading stations via pumps.

Hydrogen handling

Hydrogen produced may be vented unprocessed directly to the atmosphere or cooled, compressed and dried for use in other processes on site or sold to a customer via pipeline, cylinders or trucks. Some possible uses are hydrochloric acid or hydrogen peroxide production, desulfurization of petroleum oils and use as a fuel in boilers or fuel cells.

Energy consumption

Production of chlorine is extremely energy intensive.^[18] Energy consumption per unit weight of product is not far below that for iron and steel manufacture^[19] and greater than for the production of glass^[20] or cement.^[21]

Since electricity is an indispensable raw material for the production of chlorine, the energy consumption corresponding to the electrochemical reaction cannot be reduced. Energy savings arise primarily through applying more efficient technologies and reducing ancillary energy use.

Compounds

See also Chlorine compounds

For general references to the chloride ion (Cl⁻), including references to specific chlorides, see chloramine (NH₂Cl).^[22]

Other chlorine-containing compounds include:

• Fluorides: chlorine monofluoride (ClF), chlorine pentafluoride (ClF₅)
• Oxides: chlorine dioxide (ClO₂), dichlorine monoxide (Cl₂O), dichlorine heptoxide (Cl₂O₇)
• Acids: perchloric acid (HClO₄)

Oxidation states

Oxidation state	Name	Formula	Example compounds
−1	hydrochloric acid
0	chlorine	Cl2	elemental chlorine
+1	hypochlorites	ClO−	calcium hypochlorite
+3	sodium chlorite
+5	chlorates	ClO3−	potassium chlorate, chloric acid
+7	ammonium perchlorate

Chlorine exists in all odd numbered disproportionation:

Cl₂ + 2OH⁻ → Cl⁻ + ClO⁻ + H₂O

In hot concentrated alkali solution disproportionation continues:

2ClO⁻ → Cl⁻ + ClO₂⁻

ClO⁻ + ClO₂⁻ → Cl⁻ + ClO₃⁻

potassium chlorate can be crystallized from solutions formed by the above reactions. If their crystals are heated, they undergo the final disproportionation step.

4ClO₃⁻ → Cl⁻ + 3ClO₄⁻

This same progression from chloride to perchlorate can be accomplished by electrolysis. The anode reaction progression is:^[23]

Reaction	Electrode potential
Cl− + 2OH− → ClO− + H2O + 2e−	+0.89 volts
ClO− + 2OH− → ClO2− + H2O + 2e−	+0.67 volts
ClO2− + 2OH− → ClO3− + H2O + 2e−	+0.33 volts
ClO3− + 2OH− → ClO4− + H2O + 2e−	+0.35 volts

Each step is accompanied at the cathode by

2H₂O + 2e⁻ → 2OH⁻ + H₂          −0.83 volts

Applications and uses

Production of industrial and consumer products

Chlorine's principal applications are in the production of a wide range of industrial and consumer products.^{[24] [25]} For example, it is used in making plastics, solvents for dry cleaning and metal degreasing, textiles, agrochemicals and pharmaceuticals, insecticides, dyestuffs, etc.

Purification and disinfection

Chlorine is an important chemical for chlorination)

Chemistry

Elemental chlorine is an oxidizer. It undergoes halogen substitution reactions with lower halide salts. For example, chlorine gas bubbled through a solution of bromide or iodide anions oxidizes them to bromine and iodine respectively.

Like the other halogens, chlorine participates in 1,2-dichloroethane.

Like the other halides, chlorine undergoes electrophilic additions reactions, most notably, 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.

Chlorine is used extensively in organic compound, due to its electronegativity.

Chlorine compounds are used as intermediates in the production of a number of important commercial products that do not contain chlorine. Examples are: polytetrafluoroethylene, carboxymethyl cellulose and propylene oxide.

Other uses

Chlorine is used in the manufacture of numerous organic chlorine compounds, the most significant of which in terms of production volume are chlorobenzene, dichlorobenzenes and trichlorobenzenes.

Chlorine is also used in the production of chlorates and in bromine extraction.

Safety

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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.^[27]

Never use ABC Dry Chemical to fight a chlorine fire, the resulting chemical reaction with the ammonium phosphate will release toxic gases and/or result in an explosion. Water fogs or CAFS should be used to extinguish the material.^[27]

See also

• Chloride

References

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Hydrogen H2 | Nitrogen N2 | Oxygen O2 | Fluorine F2 | Chlorine Cl2 | Bromine Br2 | Iodine I2 | Astatine At2

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