Difference between revisions of "Calcium carbide"
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:CaC<sub>2</sub> + 2 H<sub>2</sub>O → C<sub>2</sub>H<sub>2</sub> + Ca(OH)<sub>2</sub> | :CaC<sub>2</sub> + 2 H<sub>2</sub>O → C<sub>2</sub>H<sub>2</sub> + Ca(OH)<sub>2</sub> | ||
| − | + | Impure calcium carbide, such as technical grade type, also has other calcium compounds, like calcium sulfide, calcium nitride, calcium phosphide, which in contact with water it will also produce [[phosphine]], [[ammonia]] or [[hydrogen sulfide]]. The presence of phosphine and diphosphane can lead to spontaneous ignition of the acetylene. Because it reacts with water, and releases acetylene gas, pure calcium carbide can be used as a drying agent in some limited cases. However, calcium carbide in general is a terrible drying agent, as the most common type, which is consumer grade, contains lots of impurities and will also release phosphine and ammonia which may react with various reagents, spoiling the purity of the wet compound. Acetylene may also react with some chemical compounds and tends to be quite soluble in many organic solvents. | |
Pure calcium carbide reacts slowly with anhydrous acids. | Pure calcium carbide reacts slowly with anhydrous acids. | ||
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Another method involves the reaction between finely divided calcium metal and powdered carbon (activated charcoal e.g.), at 810°C in an inert atmosphere. This reaction is highly exothermic, the calcium will not require further heating once melted.<ref>https://www.sciencemadness.org/whisper/viewthread.php?tid=2492</ref> | Another method involves the reaction between finely divided calcium metal and powdered carbon (activated charcoal e.g.), at 810°C in an inert atmosphere. This reaction is highly exothermic, the calcium will not require further heating once melted.<ref>https://www.sciencemadness.org/whisper/viewthread.php?tid=2492</ref> | ||
| − | The latter method has the advantage of obtaining a very pure product, which upon hydrolysis no longer releases the typical phosphine smell associated with the technical grade carbide. | + | The latter method has the advantage of obtaining a very pure product, which upon hydrolysis no longer releases the typical phosphine smell associated with the technical grade carbide, but rather pure acetylene, which does not carry the hazard of spontaneously igniting in air. |
While it's possible to make calcium carbide at home from raw materials, it takes lots of fuel to achieve such high temperatures, and it's cheaper to simply buy the compound. | While it's possible to make calcium carbide at home from raw materials, it takes lots of fuel to achieve such high temperatures, and it's cheaper to simply buy the compound. | ||
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===Disposal=== | ===Disposal=== | ||
| − | Calcium carbide can be neutralized by adding various types of alcohol, such as ethanol, isopropanol, resulting in acetylene, vinyl ethers, calcium alkoxides and higher alcohols from decomposition of calcium alkoxides.<ref>http://www.hgxb.com.cn/EN/abstract/abstract14646.shtml</ref> Make sure to add the carbide wastes slowly, to prevent a dangerous build-up of flammable and explosive gasses. | + | Calcium carbide can be neutralized by adding various types of alcohol, such as ethanol, isopropanol, resulting in acetylene, vinyl ethers, calcium alkoxides and higher alcohols from decomposition of calcium alkoxides.<ref>http://www.hgxb.com.cn/EN/abstract/abstract14646.shtml</ref> Make sure to add the carbide wastes slowly, to prevent a dangerous build-up of flammable and explosive gasses. Do this outside or in a fumehood with the ventilation turned on. Never perform the neutralization in a closed chamber! |
==References== | ==References== | ||
Revision as of 21:33, 22 April 2018
 OTC calcium carbide used as rodent repellent
| |
| Names | |
|---|---|
| IUPAC name
Calcium carbide
| |
| Other names
Calcium acetylide
Carbide | |
| Properties | |
| CaC2 | |
| Molar mass | 64.099 g/mol |
| Appearance | White/gray/black solid |
| Odor | Odorless (pure) Foul, garlic-like (technical grade) |
| Density | 2.22 g/cm3 |
| Melting point | 2,160 °C (3,920 °F; 2,430 K) |
| Boiling point | 2,300 °C (4,170 °F; 2,570 K) |
| Reacts | |
| Solubility | Reacts with alcohols, carboxylic acids, mineral acids Insoluble in all solvents |
| Vapor pressure | ~0 mmHg |
| Thermochemistry | |
| Std molar
entropy (S |
70 J·mol−1·K−1 |
| Std enthalpy of
formation (ΔfH |
−63 kJ/mol |
| Hazards | |
| Safety data sheet | Airgas |
| Related compounds | |
| Related compounds
|
Acetylene |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Calcium carbide is a solid chemical compound of calcium and carbon, with the formula CaC2, a carbide, that reacts with water to produce acetylene.
Calcium carbide is often referred to as simply carbide.
Contents
Properties
Chemical
Calcium carbide reacts vigorously with water to produce calcium hydroxide and acetylene gas.
- CaC2 + 2 H2O → C2H2 + Ca(OH)2
Impure calcium carbide, such as technical grade type, also has other calcium compounds, like calcium sulfide, calcium nitride, calcium phosphide, which in contact with water it will also produce phosphine, ammonia or hydrogen sulfide. The presence of phosphine and diphosphane can lead to spontaneous ignition of the acetylene. Because it reacts with water, and releases acetylene gas, pure calcium carbide can be used as a drying agent in some limited cases. However, calcium carbide in general is a terrible drying agent, as the most common type, which is consumer grade, contains lots of impurities and will also release phosphine and ammonia which may react with various reagents, spoiling the purity of the wet compound. Acetylene may also react with some chemical compounds and tends to be quite soluble in many organic solvents.
Pure calcium carbide reacts slowly with anhydrous acids.
Calcium carbide will react with nitrogen at high temperature, to form calcium cyanamide, in the Frank–Caro process:
- CaC2 + N2 → CaCN2 + C
Calcium carbide, like all ionic carbides, is a superbase. It is capable of deprotonating not just water but also alcohols, evolving acetylene.
Physical
Pure calcium carbide is white, but traces of impurities usually gives the material grey, blue or brown aspect. While the pure compound is odorless in dry air, technical grade gives off an unpleasant smell. It is insoluble in all solvents, but reacts with water and alcohols.
Availability
Technical grade calcium carbide can be found at certain construction stores, but this type contains traces of other ionic calcium compounds, such as calcium phosphide, calcium nitride, calcium sulfide, that when react with water release an unpleasant smell. Acetylene derived from calcium carbide provides the driving force behind many types of toy cannons, so calcium carbide can be obtained as a kind of fuel in stores or on websites that sell these. Purer samples can be found at lab suppliers.
Certain groundhog killers or repellents contain chunks of calcium carbide. These samples are not very pure, and also have certain additives, biocides and perfumes, like 2-undecanone, citriodiol, coated on the surface of the boulders and inside the pores of the material. These function as the groundhog repellents and do not limit the hydrolysis of the carbide as one might think.
Preparation
Calcium carbide is produced industrially in an electric arc furnace, from a mixture of calcium oxide and coke (or pure carbon) at approximately 2000 °C.
- CaO + 3 C → CaC2 + CO
Another method involves the reaction between finely divided calcium metal and powdered carbon (activated charcoal e.g.), at 810°C in an inert atmosphere. This reaction is highly exothermic, the calcium will not require further heating once melted.[1]
The latter method has the advantage of obtaining a very pure product, which upon hydrolysis no longer releases the typical phosphine smell associated with the technical grade carbide, but rather pure acetylene, which does not carry the hazard of spontaneously igniting in air.
While it's possible to make calcium carbide at home from raw materials, it takes lots of fuel to achieve such high temperatures, and it's cheaper to simply buy the compound.
Projects
- Make acetylene
- Make metal acetylides, which can be produced by bubbling acetylene through a salt solution of a metal.
- Calcium cyanamide synthesis
Handling
Safety
Calcium carbide must be handled with gloves, as while it is not as caustic as alkali metals e.g., it can still irritate the skin by reacting to the sweat and moisture. Reaction with water gives off toxic fumes, so it should be performed outside or in a fume hood; it also poses a fire hazard because of potential phosphine and diphosphane generated due to phosphorus impurities in commercial samples. In powdered form can severely irritate the eyes and mucous membrane.
Storage
Calcium carbide must be stored in dry containers and away from any moisture. As the technical grade gives off unpleasant smells, it's best to keep it in a closed container or in a well ventilated area.
Avoid storing the carbide in the basement! In case of a flood or water leak, any carbide that enters contact with water will release acetylene which, if it builds up may lead to explosion. Try to store it in the highest place from the room or in the attic if possible. Make sure rainwater doesn't leak in the storage area.
A good storage container is the common steel paint can. The can offers excellent protection against air and water. However, normal steel cans are prone to rusting, which sometimes can be a good thing, as it is an indicator that the environment where the CaC2 is stored is too wet to be safe. Airtight stainless steel cans are even better and offer good protection against most corrosive agents.
Disposal
Calcium carbide can be neutralized by adding various types of alcohol, such as ethanol, isopropanol, resulting in acetylene, vinyl ethers, calcium alkoxides and higher alcohols from decomposition of calcium alkoxides.[2] Make sure to add the carbide wastes slowly, to prevent a dangerous build-up of flammable and explosive gasses. Do this outside or in a fumehood with the ventilation turned on. Never perform the neutralization in a closed chamber!
References
- ↑ https://www.sciencemadness.org/whisper/viewthread.php?tid=2492
- ↑ http://www.hgxb.com.cn/EN/abstract/abstract14646.shtml
