出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/05/29 16:22:07」(JST)
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| Names | |||
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| IUPAC name
Hydrogen chloride[1]
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| Other names
Hydrochloric acid gas
Hydrochloride |
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| Identifiers | |||
| ATC code | A09AB03 B05XA13 |
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Beilstein Reference
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1098214 | ||
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CAS Registry Number
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7647-01-0 Y | ||
| ChEBI | CHEBI:17883 Y | ||
| ChEMBL | ChEMBL1231821 N | ||
| ChemSpider | 307 Y | ||
| EC number | 231-595-7 | ||
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Gmelin Reference
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322 | ||
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InChI
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| Jmol-3D images | Image | ||
| KEGG | D02057 Y | ||
| MeSH | Hydrochloric+acid | ||
| RTECS number | MW4025000 | ||
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SMILES
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| UNII | QTT17582CB Y | ||
| UN number | 1050 | ||
| Properties | |||
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Molecular formula
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HCl | ||
| Molar mass | 36.46 g·mol−1 | ||
| Appearance | Colorless gas | ||
| Odor | pungent | ||
| Density | 1.490 g L−1[2] | ||
| Melting point | −114.22 °C (−173.60 °F; 158.93 K) | ||
| Boiling point | −85.05 °C (−121.09 °F; 188.10 K) | ||
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Solubility in water
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823 g/L (0 °C) 720 g/L (20 °C) |
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| Solubility | soluble in methanol, ethanol, ether | ||
| Vapor pressure | 4352 kPa (at 21.1 °C)[3] | ||
| Acidity (pKa) | -3.0 [4] | ||
| Basicity (pKb) | 17.0 | ||
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Refractive index (nD)
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1.0004456 (gas) 1.254 (liquid) |
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| Viscosity | 0.311 cP (−100 °C) | ||
| Structure | |||
| Molecular shape | linear | ||
| Dipole moment | 1.05 D | ||
| Thermochemistry | |||
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Specific
heat capacity (C) |
0.7981 J K−1 g−1 | ||
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Std molar
entropy (S |
186.902 J K−1 mol−1 | ||
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Std enthalpy of
formation (ΔfH |
–92.31 kJ mol−1 | ||
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Std enthalpy of
combustion (ΔcH |
–95.31 kJ mol−1 | ||
| Hazards | |||
| SDS | JT Baker MSDS | ||
| GHS pictograms | |||
| GHS signal word | Danger | ||
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GHS hazard statements
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H280, H314, H331 | ||
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GHS precautionary statements
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P261, P280, P305+351+338, P310, P410+403 | ||
| EU Index | 017-002-00-2 | ||
| EU classification | T C | ||
| R-phrases | R23, R35 | ||
| S-phrases | (S1/2), S9, S26, S36/37/39, S45 | ||
| NFPA 704 |
0
3
1
ACID
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LD50 (Median lethal dose)
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238 mg/kg (rat, oral) | ||
| US health exposure limits (NIOSH): | |||
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PEL (Permissible)
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C 5 ppm (7 mg/m3)[5] | ||
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REL (Recommended)
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C 5 ppm (7 mg/m3)[5] | ||
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IDLH (Immediate danger)
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50 ppm[5] | ||
| Related compounds | |||
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Related compounds
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Hydrogen fluoride Hydrogen bromide |
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Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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| N verify (what is: Y/N?) | |||
| Infobox references | |||
The compound hydrogen chloride has the chemical formula HCl. At room temperature, it is a colorless gas, which forms white fumes of hydrochloric acid upon contact with atmospheric humidity. Hydrogen chloride gas and hydrochloric acid are important in technology and industry. Hydrochloric acid, the aqueous solution of hydrogen chloride, is also commonly given the formula HCl.
Hydrogen chloride is a diatomic molecule, consisting of a hydrogen atom H and a chlorine atom Cl connected by a covalent single bond. Since the chlorine atom is much more electronegative than the hydrogen atom, the covalent bond between the two atoms is quite polar. Consequently, the molecule has a large dipole moment with a negative partial charge δ− at the chlorine atom and a positive partial charge δ+ at the hydrogen atom. In part because of its high polarity, HCl is very soluble in water (and in other polar solvents).
Upon contact, H2O and HCl combine to form hydronium cations H3O+ and chloride anions Cl− through a reversible chemical reaction:
The resulting solution is called hydrochloric acid and is a strong acid. The acid dissociation or ionization constant, Ka, is large, which means HCl dissociates or ionizes practically completely in water. Even in the absence of water, hydrogen chloride can still act as an acid. For example, hydrogen chloride can dissolve in certain other solvents such as methanol, protonate molecules or ions, and serve as an acid-catalyst for chemical reactions where anhydrous (water-free) conditions are desired.
Because of its acidic nature, hydrogen chloride is corrosive, particularly in the presence of moisture.
Frozen HCl undergoes phase transition at 98.4 K. X-ray powder diffraction of the frozen material shows that the material changes from an orthorhombic structure to a cubic one during this transition. In both structures the chlorine atoms are in a face-centered array. However, the hydrogen atoms could not be located.[6] Analysis of spectroscopic and dielectric data, and determination of the structure of DCl (deuterium chloride) indicates that HCl forms zigzag chains in the solid, as does HF (see figure on right).[7]
| Temperature (°C) | 0 | 20 | 30 | 50 |
|---|---|---|---|---|
| Water | 823 | 720 | 673 | 596 |
| Methanol | 513 | 470 | 430 | |
| Ethanol | 454 | 410 | 381 | |
| Ether | 356 | 249 | 195 |
The infrared spectrum of gaseous hydrogen chloride, shown below, consists of a number of sharp absorption lines grouped around 2886 cm−1 (wavelength ~3.47 µm). At room temperature, almost all molecules are in the ground vibrational state v = 0. To promote an HCl molecule to the v = 1 state, we would expect to see an infrared absorption about 2880 cm−1. This absorption corresponding to the Q-branch is not observed due to it being forbidden by symmetry. Instead, two sets of signals (P- and R-branches) are seen owing to rotation of the molecules. Because of quantum mechanical selection rules, only certain rotational modes are permitted. They are characterized by the rotational quantum number J = 0, 1, 2, 3, ... selection rules state that ΔJ is only able to take values of ± 1.
The value of B is much smaller than ν e, such that a much smaller amount of energy is required to rotate the molecule; for a typical molecule, this lies within the microwave region. However, the vibrational energy of HCl molecule places its absorptions within the infrared region, allowing a spectrum showing the rovibrational modes of this molecule to be easily collected using an ordinary infrared spectrometer with a conventional gas cell.
Naturally abundant chlorine consists of two isotopes, 35Cl and 37Cl, in a ratio of approximately 3:1. While the spring constants are very similar, the reduced masses are different causing significant differences in the rotational energy, thus doublets are observed on close inspection of each absorption line, weighted in the same ratio of 3:1.
Most hydrogen chloride produced on an industrial scale is used for hydrochloric acid production.
In the chlor-alkali industry, brine (mixture of sodium chloride and water) solution is electrolyzed producing chlorine (Cl2), sodium hydroxide, and hydrogen (H2). The pure chlorine gas can be combined with hydrogen to produce hydrogen chloride in the presence of UV light.
As the reaction is exothermic, the installation is called an HCl oven or HCl burner. The resulting hydrogen chloride gas is absorbed in deionized water, resulting in chemically pure hydrochloric acid. This reaction can give a very pure product, e.g. for use in the food industry.
The largest production of hydrochloric acid is integrated with the formation of chlorinated and fluorinated organic compounds, e.g., Teflon, Freon, and other CFCs, as well as chloroacetic acid, and PVC. Often this production of hydrochloric acid is integrated with captive use of it on-site. In the chemical reactions, hydrogen atoms on the hydrocarbon are replaced by chlorine atoms, whereupon the released hydrogen atom recombines with the spare atom from the chlorine molecule, forming hydrogen chloride. Fluorination is a subsequent chlorine-replacement reaction, producing again hydrogen chloride.
The resulting hydrogen chloride gas is either reused directly, or absorbed in water, resulting in hydrochloric acid of technical or industrial grade.
Small amounts of HCl gas for laboratory use can be generated in a HCl generator by dehydrating hydrochloric acid with either sulfuric acid or anhydrous calcium chloride. Alternatively, HCl can be generated by the reaction of sulfuric acid with sodium chloride:[9]
This reaction occurs at room temperature. Provided there is salt remaining in the generator and it is heated above 200 degrees Celsius, the reaction proceeds to;
For such generators to function, the reagents should be dry.
HCl can also be prepared by the hydrolysis of certain reactive chloride compounds such as phosphorus chlorides, thionyl chloride (SOCl2), and acyl chlorides. For example, cold water can be gradually dripped onto phosphorus pentachloride (PCl5) to give HCl in this reaction:
High purity streams of the gas require lecture bottles or cylinders, both of which can be expensive. In comparison, the use of a generator requires only apparatus and materials commonly available in a laboratory.
Most hydrogen chloride is used in the production of hydrochloric acid. It is also an important reagent in other industrial chemical transformations, e.g.:
In the semiconductor industry, it is used to both etch semiconductor crystals and to purify silicon via trichlorosilane (SiHCl3).
It may also be used to treat cotton to delint it, and to separate it from wool.[citation needed]
In the laboratory, anhydrous forms of the gas are particularly useful for generating chloride-based Lewis acids, which must be absolutely dry for their Lewis sites to function. It can also be used to dry the corresponding hydrated forms of these materials by passing it over as they are heated; the materials would otherwise fume HCl(g) themselves and decompose. Neither can these hydrates be dried using standard desiccator methods.
Alchemists of the Middle Ages recognized that hydrochloric acid (then known as spirit of salt or acidum salis) released vaporous hydrogen chloride, which was called marine acid air. In the 17th century, Johann Rudolf Glauber used salt (sodium chloride) and sulfuric acid for the preparation of sodium sulfate, releasing hydrogen chloride gas (see production, below). In 1772, Carl Wilhelm Scheele also reported this reaction and is sometimes credited with its discovery. Joseph Priestley prepared hydrogen chloride in 1772, and in 1810 Humphry Davy established that it is composed of hydrogen and chlorine.[10]
During the Industrial Revolution, demand for alkaline substances such as soda ash increased, and Nicolas Leblanc developed a new industrial-scale process for producing the soda ash. In the Leblanc process, salt was converted to soda ash, using sulfuric acid, limestone, and coal, giving hydrogen chloride as by-product. Initially, this gas was vented to air, but the Alkali Act of 1863 prohibited such release, so then soda ash producers absorbed the HCl waste gas in water, producing hydrochloric acid on an industrial scale. Later, the Hargreaves process was developed, which is similar to the Leblanc process except sulfur dioxide, water, and air are used instead of sulfuric acid in a reaction which is exothermic overall. In the early 20th century the Leblanc process was effectively replaced by the Solvay process, which did not produce HCl. However, hydrogen chloride production continued as a step in hydrochloric acid production.
Historical uses of hydrogen chloride in the 20th century include hydrochlorinations of alkynes in producing the chlorinated monomers chloroprene and vinyl chloride, which are subsequently polymerized to make polychloroprene (Neoprene) and polyvinyl chloride (PVC), respectively. In the production of vinyl chloride, acetylene (C2H2) is hydrochlorinated by adding the HCl across the triple bond of the C2H2 molecule, turning the triple into a double bond, yielding vinyl chloride.
The "acetylene process", used until the 1960s for making chloroprene, starts out by joining two acetylene molecules, and then adds HCl to the joined intermediate across the triple bond to convert it to chloroprene as shown here:
This "acetylene process" has been replaced by a process which adds Cl2 to one of the double bonds in 1,3-butadiene instead, and subsequent elimination produces HCl instead, as well as chloroprene.
Hydrogen chloride forms corrosive hydrochloric acid on contact with water found in body tissue. Inhalation of the fumes can cause coughing, choking, inflammation of the nose, throat, and upper respiratory tract, and in severe cases, pulmonary edema, circulatory system failure, and death. Skin contact can cause redness, pain, and severe skin burns. Hydrogen chloride may cause severe burns to the eye and permanent eye damage.
The gas, being strongly hydrophilic, can be easily scrubbed from the exhaust gases of a reaction by bubbling it through water, producing useful hydrochloric acid as a byproduct.
Any equipment handling hydrogen chloride gas must be checked on a routine basis; particularly valve stems and regulators. The gas requires the use of specialized materials on all wetted parts of the flow path, as it will interact with or corrode numerous materials hydrochloric acid alone will not; such as stainless and regular polymers.
The Occupational Safety and Health Administration and the National Institute for Occupational Safety and Health have established occupational exposure limits for hydrogen chloride at a ceiling of 5 ppm (7 mg/m3).[11]
| Wikimedia Commons has media related to Hydrogen chloride. |
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| リンク元 | 「塩酸」 |
| 関連記事 | 「chloride」 |