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chlorate

 
Dictionary: chlo·rate   (klôr'āt', klōr'-) pronunciation
n.
The inorganic group ClO3 or a compound containing it.


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Columbia Encyclopedia: chlorate
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chlorate (klōr'āt, klôr'-) and perchlorate (pərklōr'āt, -klôr'-), salts of chloric acid, HClO3, and perchloric acid, HClO4, respectively.

Chloric Acid and Its Salts

Chloric acid, HClO3·7H2O, is a colorless substance that occurs only in solution. It is a strong acid and a strong oxidizing agent that decomposes if heated above 40°C. Under certain conditions it forms oxygen, water, and the explosive gas chlorine dioxide, ClO2; under other conditions it forms perchloric acid and hydrochloric acid.

Formation of Chlorates

A chlorate may be formed (together with the corresponding chloride) by heating the hypochlorite; e.g., 3Ca(ClO)2→Ca(ClO3)2+2CaCl2. This reaction takes place when chlorine gas is passed into a hot aqueous solution of a metal hydroxide; the hypochlorite is formed and decomposes almost immediately. Commercially, a chlorate is derived when a hot aqueous metal chloride solution is decomposed by electrolysis, forming chlorine gas at the anode and metal hydroxide at the cathode (with evolution of hydrogen); the chlorine reacts with the hydroxide to form the hypochlorite, which decomposes to form the chlorate.

Commercial Uses of Chlorates

The most industrially important chlorate is potassium chlorate, or chlorate of potash, KClO3; sodium chlorate, or chlorate of soda, NaClO3, is also used. Potassium chlorate is a colorless crystalline substance that melts at 356°C and decomposes violently at about 400°C. It is a powerful oxidizing agent and is used in making explosives and matches; a mixture of potassium chlorate with phosphorus, sulfur, or any of numerous organic compounds (e.g., charcoal or sugar) explodes upon friction or percussion. When a chlorate is heated, oxygen is evolved, often explosively, and the chloride is formed; e.g., 2KClO3→2KCl+3O2. The reaction proceeds controllably at lower temperatures if a catalyst, e.g., manganese dioxide, is used; this provides a convenient source of oxygen. If the chlorate is heated carefully at a lower temperature so that no oxygen is given off, the perchlorate and chloride are formed; e.g., 4KClO3→3KClO4+KCl.

Perchloric Acid and Its Salts

Perchloric acid, HClO4, is a volatile, unstable, colorless liquid that is a strong, corrosive acid and a powerful oxidizing agent, especially when hot. It explodes if heated to about 90°C or on contact with combustible materials. The monohydrate, HClO4·H2O, is fairly stable and forms needlelike crystals that melt at 50°C. It explodes if heated to 110°C. The dihydrate, HClO4·2H2O, is a stable liquid that boils at 200°C.

Formation of Perchlorates

Perchloric anhydride, or chlorine heptoxide, Cl2O7, is a colorless, oily liquid that boils at 82°C without exploding but that may be detonated by shock; it can be prepared by adding phosphorus pentoxide to cold perchloric acid. The perchlorate free radical (chlorine tetroxide, ClO4) can be prepared by adding bromine to silver perchlorate; it is extremely reactive and unstable.

Commercial Uses of Perchlorates

Perchlorates are safer to handle than chlorates; they are more stable when exposed to heat or shock. Potassium perchlorate, KClO4, is perhaps most widely used, e.g., in matches, fireworks, and explosives. It is a colorless crystalline substance that melts at about 610°C.


Veterinary Dictionary: chlorate
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As sodium or potassium chlorate, one of the original chemical herbicides but now largely superseded. Animals may be poisoned if they eat pasture or plant contaminated by the spray or the dry powder. It may also be administered accidentally because of its similarity to sodium chloride. Causes gastroenteritis with diarrhea, nitrite poisoning with anoxia and intravascular hemolysis resulting in anemic anoxia.

Wikipedia: Chlorate
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The chlorate ion
Structure and bonding in the chlorate ion

The chlorate anion has the formula ClO3. In this case, the chlorine atom is in the +5 oxidation state. "Chlorate" can also refer to chemical compounds containing this anion; chlorates are the salts of chloric acid. "Chlorate", when followed by a roman numeral in parenthesis, e.g. chlorate(VII), refers to a particular oxyanion of chlorine.

As predicted by VSEPR, chlorate anions have trigonal pyramidal structures.

Chlorates are powerful oxidizers and should be kept away from organics or easily oxidized materials. Mixtures of chlorate salts with virtually any combustible material (sugar, sawdust, charcoal, organic solvents, metals, etc) will readilly deflagrate. Chlorates were once widely used in pyrotechnics for this reason, though their use has fallen due to their instability. Most pyrotechnic applications which formerly used chlorates in the past now use perchlorates instead.

Contents

Structure and bonding

The chlorate ion cannot be satisfactorily represented by just one Lewis structure, since all the Cl-O bonds are the same length (1.49 Å in potassium chlorate[1]), and the chlorine atom is hypervalent. Instead, it is often thought of as a hybrid of multiple resonance structures:

Resonance structures of the chlorate ion

Preparation

Laboratory

Metal chlorates can be prepared by adding chlorine to hot metal hydroxides, for example, KClO3:

3 Cl2 + 6 KOH → 5 KCl + KClO3 + 3 H2O

In this reaction chlorine undergoes disproportionation, both reduction and oxidation. Chlorine, oxidation number 0, forms chloride Cl (oxidation number −1) and chlorate(V) ClO3 (oxidation number +5). Reaction of dilute aqueous sodium hydroxide with chlorine produces the chloride and hypochlorite (oxidation number +1).

Industrial

The industrial scale synthesis for sodium chlorate starts from aqueous sodium chloride solution (brine) rather than chlorine gas. If equipment for electrolysis does not prevent a mixing of the chlorine evolved and the sodium hydroxide is as described in chlorine, then the disproportionation reaction described above occurs. The heating of the reactants to 50-70°C is performed by the electrical power used for electrolysis.[citation needed]

Compounds (salts)

Examples of chlorates include:

Other oxyanions

If a Roman numeral in brackets follows the word "chlorate", this indicates the oxyanion contains chlorine in the indicated oxidation state, namely:

Common name Stock name Oxidation state Formula
Hypochlorite Chlorate(I) +1 ClO
Chlorite Chlorate(III) +3 ClO2
Chlorate Chlorate(V) +5 ClO3
Perchlorate Chlorate(VII) +7 ClO4

Using this convention, "chlorate" means any chlorine oxyanion. Commonly, "chlorate" refers only to chlorine in the +5 oxidation state.

References

  1. ^ J. Danielsen, A. Hazell, F. K. Larsen (1981). "The structure of potassium chlorate at 77 and 298 K". Acta Cryst. B37: 913-915. doi:10.1107/S0567740881004573. 

 
 

 

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Dictionary. The American Heritage® Dictionary of the English Language, Fourth Edition Copyright © 2007, 2000 by Houghton Mifflin Company. Updated in 2009. Published by Houghton Mifflin Company. All rights reserved.  Read more
Columbia Encyclopedia. The Columbia Electronic Encyclopedia, Sixth Edition Copyright © 2003, Columbia University Press. Licensed from Columbia University Press. All rights reserved. www.cc.columbia.edu/cu/cup/ Read more
Veterinary Dictionary. Saunders Comprehensive Veterinary Dictionary 3rd Edition. Copyright © 2007 by D.C. Blood, V.P. Studdert and C.C. Gay, Elsevier. All rights reserved.  Read more
Wikipedia. This article is licensed under the Creative Commons Attribution/Share-Alike License. It uses material from the Wikipedia article "Chlorate" Read more