| Dictionary: potassium chlorate |
| 5min Related Video: potassium chlorate |
| Chemistry Dictionary: potassium chlorate |
A colourless crystalline compound, KClO3, which is soluble in water and moderately soluble in ethanol; monoclinic; r.d. 2.32; m.p. 356°C; decomposes above 400°C giving off oxygen. The industrial route to potassium chlorate involves the fractional crystallization of a solution of potassium chloride and sodium chlorate but it may also be prepared by electrolysis of hot concentrated solutions of potassium chloride. It is a powerful oxidizing agent finding applications in weedkillers and disinfectants and, because of its ability to produce oxygen, it is used in explosives, pyrotechnics, and matches.
| Medical Dictionary: potassium chlorate |
A poisonous crystalline compound used as an oxidizing agent and a disinfectant.
| WordNet: potassium chlorate |
The noun has one meaning:
Meaning #1:
a white salt (KClO3) used in matches, fireworks, and explosives; also used as a disinfectant and bleaching agent
| Wikipedia: Potassium chlorate |
| Potassium Chlorate | |
|---|---|
| Other names | Potassium chlorate(V), Potcrate |
| Identifiers | |
| CAS number | 3811-04-9 |
| PubChem | 6426889 |
| EC number | 223-289-7 |
| UN number | 1485 |
| RTECS number | FO0350000 |
| Properties | |
| Molecular formula | KCLO3 |
| Molar mass | 122.55 g/mol |
| Appearance | White crystals or powder |
| Density | 2.34 g/cm3 |
| Melting point |
356 °C |
| Boiling point |
400 °C decomp. |
| Solubility in water | 7.19 g/100 ml (20 °C) 57 g/100 mL (100 °C) |
| Solubility | insoluble in acetone, liquid ammonia |
| Refractive index (nD) | 1.40835 |
| Structure | |
| Crystal structure | monoclinic |
| Hazards | |
| MSDS | ICSC 0548 |
| EU Index | 017-004-00-3 |
| EU classification | Oxidant (O) Harmful (Xn) Dangerous for the environment (N) |
| R-phrases | R9, R22, R51/53 |
| S-phrases | (S2), S13, S16, S27, S61 |
| NFPA 704 | |
| Flash point | 400 °C |
| LD50 | 1870 mg/kg |
| Related compounds | |
| Other anions | Potassium bromate Potassium iodate |
| Other cations | Ammonium chlorate Sodium chlorate Barium chlorate |
| Related compounds | Potassium chloride Potassium hypochlorite Potassium chlorite Potassium perchlorate |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Potassium chlorate is a compound containing potassium, chlorine and oxygen, with the molecular formula KClO3. In pure form, it is a white crystalline substance. It is the most common chlorate in industrial use, and is usually present in well-stocked laboratories. It is used
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Potassium chlorate was one key ingredient in early firearms percussion caps (primers). It continues in that application, where not supplanted by potassium perchlorate.
Chlorate-based propellants are more efficient than traditional gunpowder and are less susceptible to damage by water. However, they can be extremely unstable in the presence of sulfur or phosphorus and are much more expensive. Chlorate propellants must be used only in equipment designed for them; failure to follow this precaution is a common source of accidents. Potassium chlorate, often in combination with silver fulminate, is used in trick noise-makers known as "crackers", "snappers", "pop-its", or "bang-snaps", a popular type of novelty firework.
When mixed with a suitable fuel, it may form an explosive material, a so-called Sprengel explosive. The hygroscopic and slightly weaker sodium chlorate is sometimes used as a safer and less expensive substitute for potassium chlorate. In World War I, mixes of potassium chlorate with plasticizers (such as wax) were the most common type of plastic explosive used, often filling grenades and other munitions. When used in explosives as an oxidizer, the explosive is low order meaning it burns rapidly rather than explodes. When mixed with a plasticizer, it may become high order, requiring a blasting cap (generally a commercial #8) to detonate properly. Potassium chlorate is also used in some formulas of gunpowder, generally replacing the less powerful potassium nitrate.
Potassium chlorate is often used in high school and college laboratories to generate oxygen gas[citation needed]; it is a far cheaper source than a pressurized or cryogenic oxygen tank. Potassium chlorate will readily decompose if heated in contact with a catalyst, typically manganese (IV) dioxide (MnO2). Thus, it may be simply placed in a test tube and heated over a burner. If the test tube is equipped with a one-holed stopper and hose, warm oxygen can be drawn off. The reaction is as follows:
2KClO3(s) + heat → 3O2(g) + 2KCl(s)
The safe performance of this reaction requires very pure reagents and careful temperature control. Molten potassium chlorate is an extremely powerful oxidizer and will spontaneously react with many common materials. Explosions have resulted from liquid chlorates spattering into the latex or PVC tubes of oxygen generators, as well as from contact between chlorates and hydrocarbon sealing greases. Impurities in potassium chlorate itself can also cause problems. When working with a new batch of potassium chlorate, it is advisable to take a small sample (~ 1 gram) and heat it strongly on an open glass plate. Contamination may cause this small quantity to explode, indicating that the chlorate should be discarded.
Potassium chlorate is used in chemical oxygen generators (also called chlorate candles or oxygen candles), employed as oxygen-supply systems of e.g. aircraft, space stations, and submarines, and has been responsible for at least one plane crash. A fire on the space station Mir was also traced to this substance. The decomposition of potassium chlorate was also used to provide the oxygen supply for limelights.
Potassium chlorate is used also as a pesticide. In Finland it was sold under trade name Fegabit.
Potassium chlorate should be handled with care. It reacts vigorously, and in some cases spontaneously ignites or explodes, when mixed with many combustible materials. It will burn vigorously in combination with virtually any combustible material, even those which are considered to by only slightly flammable normally (including ordinary dust and lint). Mixtures of potassium chlorate and a fuel can be ignited by contact with sulfuric acid and this reagent should be kept away from potassium chlorate. Sulfur should be avoided in pyrotechnic compositions containing potassium chlorate, as these mixtures are prone to spontaneous deflagration. Most sulfur contains trace quantities of sulfur-containing acids, and these can cause spontaneous ignition - "Flowers of sulfur" or "sublimed sulfur", despite the overall high purity, contains significant amounts of sulfur acids. Also, mixtures of potassium chlorate with any compound with ignition promoting properties (ex. antimony(III) sulfide) are very dangerous to prepare, as they are extremely shock sensitive.
On an industrial scale, potassium chlorate is produced by the electrolysis of a sodium chloride solution to form sodium chlorate, which is reacted with potassium chloride to precipitate potassium chlorate. The resultant sodium chloride is returned to the mother liquor for electrolysis.
KClO3 can also be produced on a smaller scale by the thermal disproportionation of a hypochlorite to its respective chlorate and chloride by boiling, then adding KCl. This reaction should be done in a fume hood due to the production of chlorine and chlorine dioxide gas.
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