Chlorine (Cl)
halogenGas
标准原子量
35.45 u [35.446, 35.457]电子排布
[Ne] 3s2 3p5熔点
-101.5 °C沸点
-34.04 °C密度
3.214 kg/m³氧化态
−1, +1, +2, +3, +4, +5, +6, +7电负性（鲍林）
3.16第一电离能
12.967633 eV发现年份
1774原子半径
100 pm详细信息
Chlorine is a reactive halogen and a yellow-green diatomic gas, Cl₂, under ordinary conditions. It is a strong oxidizing agent and occurs naturally mainly as chloride salts, especially in seawater and evaporite minerals. Chlorine chemistry is central to water disinfection, inorganic chlorides, chlorinated solvents, polymers, and many industrial oxidation and substitution processes. The element has two stable isotopes, ³⁵Cl and ³⁷Cl.
It is a member of the halogen (salt-forming) group of elements and is obtained from chlorides by the action of oxidizing agents and more often by electrolysis; it is a greenish-yellow gas, combining directly with nearly all elements. At 10°C one volume of water dissolves 3.10 volumes of chlorine, at 30°C only 1.77 volumes.
The name derives from the Greek chloros for "pale green" or "greenish yellow" colour of the element. It was discovered by the Swedish pharmacist and chemist Carl-Wilhelm Scheele in 1774. In 1810, the English chemist Humphry Davy proved it was an element.
Since it combines directly with nearly every element, chlorine is never found free in nature. Chlorine was first produced by Carl Wilhelm Scheele, a Swedish chemist, when he combined the mineral pyrolusite (MnO2) with hydrochloric acid (HCl) in 1774. Although Scheele thought the gas produced in his experiment contained oxygen, Sir Humphry Davy proved in 1810 that it was actually a distinct element. Today, most chlorine is produced through the electrolysis of aqueous sodium chloride (NaCl).
From the Greek word chloro, greenish yellow. Discovered in 1774 by Scheele, who thought it contained oxygen. Chlorine was named in 1810 by Davy, who insisted it was an element.
Pure chlorine is a dense yellow-green gas with a sharp, irritating odor. It condenses to an amber liquid under pressure or cooling and freezes to a pale solid. The gas is visibly colored even at moderate concentrations in laboratory vessels.
Elemental chlorine, Cl₂, is used chiefly as a chemical intermediate rather than as an end product. Major uses include production of vinyl chloride for polyvinyl chloride, manufacture of chlorinated solvents and intermediates, bleaching of some pulp and textile streams, and synthesis of inorganic chlorides. Chlorine and hypochlorite solutions are widely used for drinking-water, wastewater, and swimming-pool disinfection. Hydrochloric acid, HCl, made directly or as a by-product, is also an important industrial reagent.
Chlorine is commonly used as an antiseptic and is used to make drinking water safe and to treat swimming pools. Large amounts of chlorine are used in many industrial processes, such as in the production of paper products, plastics, dyes, textiles, medicines, antiseptics, insecticides, solvents and paints.
Two of the most familiar chlorine compounds are sodium chloride (NaCl) and hydrogen chloride (HCl). Sodium chloride, commonly known as table salt, is used to season food and in some industrial processes. Hydrogen chloride, when mixed with water (H2O), forms hydrochloric acid, a strong and commercially important acid. Other chlorine compounds include: chloroform (CHCl3), carbon tetrachloride (CCl4), potassium chloride (KCl), lithium chloride (LiCl), magnesium chloride (MgCl2) and chlorine dioxide (ClO2).
Chlorine is a very dangerous material. Liquid chlorine burns the skin and gaseous chlorine irritates the mucus membranes. Concentrations of the gas as low as 3.5 parts per million can be detected by smell while concentrations of 1000 parts per million can be fatal after a few deep breaths.
Chlorine is widely used in making many everyday products. It is used for producing safe drinking water the world over. Even the smallest water supplies are now usually chlorinated.
It is also extensively used in the production of paper products, dyestuffs, textiles, petroleum products, medicines, antiseptics, insecticides, food, solvents, paints, plastics, and many other consumer products.
Most of the chlorine produced is used in the manufacture of chlorinated compounds for sanitation, pulp bleaching, disinfectants, and textile processing. Further use is in the manufacture of chlorates, chloroform, carbon tetrachloride, and in the extraction of bromine.
Organic chemistry demands much from chlorine, both as an oxidizing agent and in substitution, since it often brings many desired properties in an organic compound when substituted for hydrogen, as in one form of synthetic rubber.
Isotopes in Earth/Planetary Science
Because molecules, atoms, and ions of the stable isotopes of chlorine possess slightly different physical and chemical properties, they commonly will be fractionated during physical, chemical, and biological processes, giving rise to variations in isotopic abundances and in atomic weights. There are substantial variations in the isotopic abundances of chlorine in natural terrestrial materials (Fig. IUPAC.17.1). These variations are useful for investigating the origin of substances and studying environmental, hydrological, and geological processes. Chlorine is subject to isotopic fractionation by physical and chemical processes. Variations in isotopic compositions of stable chlorine isotopes provide evidence for ultrafiltration and crystallization of brines and indicate sources of chlorine-bearing contaminants, such as solvents and rocket fuels, in the environment [151] H. G. M. Eggenkamp, R. Kreulen, A. F. Koster Van Groos. Geochim. Cosmochim. Acta59, 5169 (1995)., [152] M. A. Stewart, A. J. Spivack. Rev. Mineral. Geochem.55, 231 (2004)..
Isotopes in Forensic Science and Anthropology
Analyses of chlorine isotopes and other environmental tracers can help to identify whether an environmental contaminant is of anthropogenic origin or naturally occurring. For example, perchlorate (ClO4 -) can be of anthropogenic origin and is also found naturally. Perchlorate is a widespread groundwater contaminant that can interfere with hormone production in the thyroid gland by displacing iodide. Both the stable chlorine isotope-amount ratio n(37Cl)/n(35Cl) and the mole fraction of 36Cl, n(36Cl)/n(Cl), can provide useful information about origins of perchlorate in the environment (Fig. IUPAC.17.2). Such information may be important for legal reasons and for remediation of contaminated areas [152] M. A. Stewart, A. J. Spivack. Rev. Mineral. Geochem.55, 231 (2004)., [153] J. K. Böhlke, N. C. Sturchio, B. Gu, J. Horita, G. M. Brown, W. A. Jackson, J. R. Batista, P. B. Hatzinger. Anal. Chem.77, 7838 (2005)..
Isotopes in Geochronology
Radioactive 36Cl provides a useful tool to determine ages in geology and hydrology. Some radioactive 36Cl is cosmogenic and enters the terrestrial environment in precipitation. Because of its long half-life of 3.01×105 years, the level of 36Cl in aquifers can be measured and used to estimate ages (on the order of 105 to 106 years) of old meteoric groundwater (water that was originally precipitation) [155] F. M. Phillips. “Chlorine-36”, in Environmental Tracers in Subsurface Hydrology, P. G. Cook and A. L. Herczeg (Eds.), Kluwer Academic Publishers, Boston MA (2000)..
Thermonuclear bomb tests in the ocean produced large amounts of 36Cl by neutron reactions with 35Cl in seawater. This was especially prevalent in the late 1950s. Large amounts of this anthropogenic 36Cl were distributed throughout the atmosphere, deposited with precipitation, and incorporated into terrestrial soils and groundwater. This enriched 36Cl has been used as a tracer of meteoric water from that era [156] F. M. Phillips, J. L. Mattick, T. A. Duval, D. Elmore, P. W. Kubik. Water Resour. Res.24, 877 (1988)..
Chlorine commonly forms chloride compounds in the −1 oxidation state, including sodium chloride, NaCl, hydrogen chloride, HCl, and many metal chlorides. It also forms positive oxidation states in oxyanions such as hypochlorite, ClO⁻, chlorite, ClO₂⁻, chlorate, ClO₃⁻, and perchlorate, ClO₄⁻. Important molecular compounds include chlorine dioxide, ClO₂, and phosphorus trichloride, PCl₃. Organic chlorides range from simple chloromethane, CH₃Cl, to complex polymers and pharmaceuticals.
See more information at the Chlorine compound page.
Chlorine, Cl₂, is acutely toxic by inhalation and strongly irritating to eyes, skin, and the respiratory tract. It reacts with moisture in tissues to form acidic and oxidizing species. Concentrated hypochlorite solutions and chlorine dioxide, ClO₂, are hazardous oxidizers, and mixing hypochlorite with acids can release chlorine gas. Many chloride salts are low-hazard at ordinary exposure levels, but toxicity depends strongly on the accompanying cation or organic group.
Chlorine is a respiratory irritant. The gas irritates the mucus membranes and the liquid burns the skin. As little as 3.5 ppm can be detected as an odor, and 1000 ppm is likely to be fatal after a few deep breaths. In fact, chlorine was used as a war gas in 1915.
Chlorine is abundant in the environment mainly as chloride, Cl⁻, dissolved in seawater, brines, soils, and biological fluids. Marine aerosols, evaporite deposits, volcanic gases, and weathering move chlorine through natural cycles. Reactive chlorine compounds are formed naturally in the atmosphere and by organisms, but industrial organochlorines have added persistent pollutants in some settings. Chloride is mobile in water and is not readily removed by ordinary soil adsorption.
Chlorine is produced industrially by electrolysis of brine, usually together with sodium hydroxide, NaOH, and hydrogen, H₂, in the chlor-alkali process. The economics are closely tied to demand for caustic soda and for chlorine-consuming products such as polyvinyl chloride and isocyanates. Because chlorine gas is hazardous to transport, large users are often integrated with production sites or consume it nearby. Recycling is indirect: chloride from wastes may be recovered in salts or converted through industrial processes, but much chlorine ultimately disperses as chloride.
In nature it is found in the combined state only, chiefly with sodium as common salt (NaCl), carnallite, and sylvite.
Chlorine is a moderately abundant cosmic element made mainly in massive stars and supernova-related nucleosynthesis. It is less abundant than neighboring elements such as sulfur and argon. In planetary materials it is strongly lithophile and volatile relative to many rock-forming elements, occurring as chlorides, brines, and volcanic gases. Chlorine-bearing salts have been detected or inferred on several planetary bodies.
- Chlorine gas was used as a chemical weapon in the First World War.
- Natural chlorine has a stable isotope ratio that is useful in isotope geochemistry.
- Dry chlorine is less corrosive to many metals than moist chlorine.
- Common table salt contains chlorine as chloride, not as elemental Cl₂.
- Perchlorate salts can persist in arid soils and interfere with iodide uptake.
- Chlorine is liquefied commercially for storage and transport under pressure.
图片
性质
物理性质
- 原子半径（经验值）
- 100 pm 比较所有元素的原子半径（经验值） →
- 共价半径
- 102 pm 比较所有元素的共价半径 →
- 范德华半径
- 175 pm 比较所有元素的范德华半径 →
- 密度
- 3.214 kg/m³ 比较所有元素的密度 →
- 摩尔体积
- 0.0187 L/mol
- 标准温度和压力下的物相
- 气态 比较所有元素的标准温度和压力下的物相 →
- 熔点
- -101.5 °C 比较所有元素的熔点 →
- 沸点
- -34.04 °C 比较所有元素的沸点 →
- 热导率
- 0.009 W/(m·K) 比较所有元素的热导率 →
- 比热容
- 0.479 J/(g·K) 比较所有元素的比热容 →
- 摩尔热容
- 33.949 J/(mol·K) 比较所有元素的摩尔热容 →
- 晶体结构
- 正交 比较所有元素的晶体结构 →
化学性质
- 电负性（鲍林）
- 3.16 比较所有元素的电负性（鲍林） →
- 电负性（Allen）
- 2.869
- 电子亲和能
- 3.6127 eV
- 第一电离能
- 12.967633 eV 比较所有元素的第一电离能 →
- 第二电离能
- 23.813722 eV 比较所有元素的第二电离能 →
- 第三电离能
- 39.800137 eV 比较所有元素的第三电离能 →
- 第四电离能
- 53.240183 eV 比较所有元素的第四电离能 →
- 第五电离能
- 67.680233 eV 比较所有元素的第五电离能 →
- 氧化态
- −1, +1, +2, +3, +4, +5, +6, +7 比较所有元素的氧化态 →
- 价电子
- 7 比较所有元素的价电子 →
- 电子排布
- [Ne] 3s2 3p5
热力学性质
- 临界点（温度）
- 143.9 °C
- 临界点（压力）
- 7.991e+6 Pa
- 熔化热
- 0.0664352 eV 比较所有元素的熔化热 →
- 汽化热
- 0.21153547 eV 比较所有元素的汽化热 →
- 原子化热
- 1.261129 eV
- 原子化焓
- 1.257211 eV
核性质
- 质子
- 17 比较所有元素的质子 →
- 中子
- 18 比较所有元素的中子 →
- 已知同位素
- 25 比较所有元素的已知同位素 →
- 稳定同位素
- 2 比较所有元素的稳定同位素 →
- 最稳定同位素
- Cl-35
- 发现年份
- 1774
丰度
- 丰度（地壳）
- 145 mg/kg 比较所有元素的丰度（地壳） →
- 丰度（海洋）
- 1.94 × 104 mg/L 比较所有元素的丰度（海洋） →
晶体结构
- 晶格常数a
- 624 pm
电子结构
- 各电子层电子数
- 2, 8, 7 比较所有元素的各电子层电子数 →
标识符
- CAS登记号
- 7782-50-5 比较所有元素的CAS登记号 →
- 谱项符号
- 2P°3/2
- InChI
- InChI=1S/Cl
- InChI Key
- ZAMOUSCENKQFHK-UHFFFAOYSA-N
电子排布 实测值
Cl: 3s² 3p⁵[Ne] 3s² 3p⁵1s² 2s² 2p⁶ 3s² 3p⁵原子模型
不同同位素的中子数、质量和稳定性不同，但中性原子的电子排布不变。
原子模型示意图，未按比例绘制。
原子指纹
发射 / 吸收光谱
同位素分布
| 质量数 | 原子质量（u） | 天然丰度 | 半衰期 |
|---|---|---|---|
| 35 稳定 | 34.968852682 ± 0.000000037 | 75.7600% | 稳定 |
| 37 稳定 | 36.965902602 ± 0.000000055 | 24.2400% | 稳定 |
物相 / 状态
原因: 高于沸点（-34.04 °C）59.0 °C
示意图，未按比例绘制
相变点
相变能
在熔点熔化1 mol物质所需的能量
在沸点汽化1 mol物质所需的能量
密度
标准条件下
按当前温度T，通过理想气体定律估算
高级
原子光谱
已显示10项，共17项。 按离子电荷升序排列。
收录谱线 ?
| 离子 | 电荷 | 谱线总数 | 跃迁概率 | 能级标记 |
|---|---|---|---|---|
| Cl I | 0 | 221 | 99 | 100 |
| Cl II | +1 | 292 | 221 | 221 |
| Cl III | +2 | 192 | 166 | 166 |
| Cl IV | +3 | 73 | 42 | 45 |
| Cl V | +4 | 27 | 6 | 6 |
| Cl VI | +5 | 1 | 1 | 1 |
| Cl VII | +6 | 28 | 28 | 28 |
| Cl VIII | +7 | 5 | 5 | 5 |
| Cl IX | +8 | 3 | 3 | 3 |
| Cl X | +9 | 11 | 11 | 11 |
收录能级 ?
| 离子 | 电荷 | 能级 |
|---|---|---|
| Cl I | 0 | 379 |
| Cl II | +1 | 275 |
| Cl III | +2 | 83 |
| Cl IV | +3 | 41 |
| Cl V | +4 | 29 |
| Cl VI | +5 | 67 |
| Cl VII | +6 | 47 |
| Cl VIII | +7 | 29 |
| Cl IX | +8 | 57 |
| Cl X | +9 | 15 |
离子半径
| 电荷 | 配位 | 自旋 | 半径 |
|---|---|---|---|
| -1 | 6 | 暂无 | 181 pm |
| +5 | 3 | 暂无 | 12 pm |
| +7 | 4 | 暂无 | 8 pm |
| +7 | 6 | 暂无 | 27 pm |
化合物
同位素 (2)
| 质量数 | 原子质量（u） | 天然丰度 | 半衰期 | 衰变方式 | |
|---|---|---|---|---|---|
| 35 稳定 | 34.968852682 ± 0.000000037 | 75.7600% ± 0.1000% | 稳定 | stable | |
| 37 稳定 | 36.965902602 ± 0.000000055 | 24.2400% ± 0.1000% | 稳定 | stable |
谱线
已显示50项，共207项。 默认仅显示具有实测强度的谱线。
| 波长（nm） | 强度 | 电离级 | 类型 | 跃迁 | 准确度 | 来源 | |
|---|---|---|---|---|---|---|---|
| 479.4556 nm | 99000 | Cl II | emission | 3s2.3p3.(4S*).4s 5S* → 3s2.3p3.(4S*).4p 5P | 实测值 | NIST | |
| 542.3257 nm | 99000 | Cl II | emission | 3s2.3p3.(4S*).3d 5D* → 3s2.3p3.(4S*).4p 5P | 实测值 | NIST | |
| 489.6783 nm | 81000 | Cl II | emission | 3s2.3p3.(2D*).4s 3D* → 3s2.3p3.(2D*).4p 3F | 实测值 | NIST | |
| 521.7945 nm | 56000 | Cl II | emission | 3s2.3p3.(4S*).4s 3S* → 3s2.3p3.(4S*).4p 3P | 实测值 | NIST | |
| 490.4776 nm | 47000 | Cl II | emission | 3s2.3p3.(2D*).4s 3D* → 3s2.3p3.(2D*).4p 3F | 实测值 | NIST | |
| 481.007 nm | 29000 | Cl II | emission | 3s2.3p3.(4S*).4s 5S* → 3s2.3p3.(4S*).4p 5P | 实测值 | NIST | |
| 491.773 nm | 26000 | Cl II | emission | 3s2.3p3.(2D*).4s 3D* → 3s2.3p3.(2D*).4p 3F | 实测值 | NIST | |
| 507.8267 nm | 26000 | Cl II | emission | 3s2.3p3.(2D*).4s 3D* → 3s2.3p3.(2D*).4p 3D | 实测值 | NIST | |
| 386.0828 nm | 25000 | Cl II | emission | 3s2.3p3.(4S*).4p 5P → 3s2.3p3.(4S*).4d 5D* | 实测值 | NIST | |
| 522.1362 nm | 23000 | Cl II | emission | 3s2.3p3.(4S*).4s 3S* → 3s2.3p3.(4S*).4p 3P | 实测值 | NIST | |
| 544.3375 nm | 19000 | Cl II | emission | 3s2.3p3.(4S*).3d 5D* → 3s2.3p3.(4S*).4p 5P | 实测值 | NIST | |
| 481.948 nm | 16000 | Cl II | emission | 3s2.3p3.(4S*).4s 5S* → 3s2.3p3.(4S*).4p 5P | 实测值 | NIST | |
| 539.2125 nm | 15000 | Cl II | emission | 3s2.3p3.(2D*).4s 1D* → 3s2.3p3.(2D*).4p 1F | 实测值 | NIST | |
| 478.132 nm | 13000 | Cl II | emission | 3s2.3p3.(2P*).4s 3P* → 3s2.3p3.(2P*).4p 3D | 实测值 | NIST | |
| 385.0988 nm | 10000 | Cl II | emission | 3s2.3p3.(4S*).4p 5P → 3s2.3p3.(4S*).4d 5D* | 实测值 | NIST | |
| 499.5473 nm | 10000 | Cl II | emission | 3s2.3p3.(2D*).3d 3F* → 3s2.3p3.(2D*).4p 3D | 实测值 | NIST | |
| 542.3516 nm | 10000 | Cl II | emission | 3s2.3p3.(4S*).3d 5D* → 3s2.3p3.(4S*).4p 5P | 实测值 | NIST | |
| 544.4217 nm | 10000 | Cl II | emission | 3s2.3p3.(4S*).3d 5D* → 3s2.3p3.(4S*).4p 5P | 实测值 | NIST | |
| 385.1374 nm | 7900 | Cl II | emission | 3s2.3p3.(4S*).4p 5P → 3s2.3p3.(4S*).4d 5D* | 实测值 | NIST | |
| 725.6618 nm | 7500 | Cl I | emission | 3s2.3p4.(3P).4s 4P → 3s2.3p4.(3P).4p 4S* | 实测值 | NIST | |
| 545.7037 nm | 5600 | Cl II | emission | 3s2.3p3.(4S*).3d 5D* → 3s2.3p3.(4S*).4p 5P | 实测值 | NIST | |
| 741.4118 nm | 5000 | Cl I | emission | 3s2.3p4.(3P).4s 4P → 3s2.3p4.(3P).4p 2P* | 实测值 | NIST | |
| 386.099 nm | 4400 | Cl II | emission | 3s2.3p3.(4S*).4p 5P → 3s2.3p3.(4S*).4d 5D* | 实测值 | NIST | |
| 476.8651 nm | 4300 | Cl II | emission | 3s2.3p3.(2P*).4s 3P* → 3s2.3p3.(2P*).4p 3D | 实测值 | NIST | |
| 384.5639 nm | 3900 | Cl II | emission | 3s2.3p3.(4S*).4p 5P → 3s2.3p3.(4S*).4d 5D* | 实测值 | NIST | |
| 384.5362 nm | 3100 | Cl II | emission | 3s2.3p3.(4S*).4p 5P → 3s2.3p3.(4S*).4d 5D* | 实测值 | NIST | |
| 380.5174 nm | 1900 | Cl II | emission | 3s2.3p3.(2D*).4p 3D → 3s2.3p3.(2D*).4d 3F* | 实测值 | NIST | |
| 609.468 nm | 1900 | Cl II | emission | 3s2.3p3.(2D*).4s 1D* → 3s2.3p3.(2D*).4p 1P | 实测值 | NIST | |
| 384.5788 nm | 1500 | Cl II | emission | 3s2.3p3.(4S*).4p 5P → 3s2.3p3.(4S*).4d 5D* | 实测值 | NIST | |
| 391.3866 nm | 1500 | Cl II | emission | 3s2.3p3.(2D*).4p 3F → 3s2.3p3.(2D*).4d 3F* | 实测值 | NIST | |
| 380.9459 nm | 1300 | Cl II | emission | 3s2.3p3.(2D*).4p 3D → 3s2.3p3.(2D*).4d 3F* | 实测值 | NIST | |
| 385.1651 nm | 1200 | Cl II | emission | 3s2.3p3.(4S*).4p 5P → 3s2.3p3.(4S*).4d 5D* | 实测值 | NIST | |
| 391.6632 nm | 1100 | Cl II | emission | 3s2.3p3.(2D*).4p 3F → 3s2.3p3.(2D*).4d 3F* | 实测值 | NIST | |
| 386.1378 nm | 1000 | Cl II | emission | 3s2.3p3.(4S*).4p 5P → 3s2.3p3.(4S*).4d 5D* | 实测值 | NIST | |
| 399.1367 nm | 700 | Cl III | emission | 3s2.3p2.(3P).3d 4P → 3s2.3p2.(3P).4p 4P* | 实测值 | NIST | |
| 401.8351 nm | 600 | Cl III | emission | 3s2.3p2.(3P).3d 4P → 3s2.3p2.(3P).4p 4P* | 实测值 | NIST | |
| 405.893 nm | 600 | Cl III | emission | 3s2.3p2.(3P).3d 4P → 3s2.3p2.(3P).4p 4P* | 实测值 | NIST | |
| 410.4082 nm | 500 | Cl III | emission | 3s2.3p2.(3P).3d 4P → 3s2.3p2.(3P).4p 4P* | 实测值 | NIST | |
| 410.6764 nm | 500 | Cl III | emission | 3s2.3p2.(3P).3d 4P → 3s2.3p2.(3P).4p 4P* | 实测值 | NIST | |
| 436.3268 nm | 100 | Cl I | emission | 3s2.3p4.(3P).4s 4P → 3s2.3p4.(3P).5p 4D* | 实测值 | NIST | |
| 436.9498 nm | 100 | Cl I | emission | 3s2.3p4.(3P).4s 4P → 3s2.3p4.(3P).5p 2D* | 实测值 | NIST | |
| 437.9896 nm | 100 | Cl I | emission | 3s2.3p4.(3P).4s 4P → 3s2.3p4.(3P).5p 4D* | 实测值 | NIST | |
| 438.9751 nm | 100 | Cl I | emission | 3s2.3p4.(3P).4s 4P → 3s2.3p4.(3P).5p 4D* | 实测值 | NIST | |
| 443.8488 nm | 100 | Cl I | emission | 3s2.3p4.(3P).4s 4P → 3s2.3p4.(3P).5p 4P* | 实测值 | NIST | |
| 452.6182 nm | 100 | Cl I | emission | 3s2.3p4.(3P).4s 2P → 3s2.3p4.(3P).5p 2P* | 实测值 | NIST | |
| 439.0403 nm | 90 | Cl I | emission | 3s2.3p4.(3P).4s 4P → 3s2.3p4.(3P).5p 4D* | 实测值 | NIST | |
| 440.302 nm | 90 | Cl I | emission | 3s2.3p4.(3P).4s 4P → 3s2.3p4.(3P).5p 4P* | 实测值 | NIST | |
| 447.5304 nm | 90 | Cl I | emission | 3s2.3p4.(3P).4s 4P → 3s2.3p4.(3P).5p 2D* | 实测值 | NIST | |
| 460.0977 nm | 80 | Cl I | emission | 3s2.3p4.(3P).4s 2P → 3s2.3p4.(3P).5p 2P* | 实测值 | NIST | |
| 466.1208 nm | 80 | Cl I | emission | 3s2.3p4.(3P).4s 2P → 3s2.3p4.(3P).5p 2P* | 实测值 | NIST |
扩展性质
共价半径（扩展）
- 共价半径（Pyykkö）
- 99 pm
- 共价半径（Pyykkö，双键）
- 95 pm
- 共价半径（Pyykkö，三键）
- 93 pm
- 共价半径（Bragg）
- 105 pm
范德华半径
- Bondi
- 175 pm
- Batsanov
- 180 pm
- Alvarez
- 182 pm
- UFF
- 394.7 pm
- MM3
- 207 pm
- Dreiding
- 395.03 pm
- Rowland–Taylor
- 176 pm
原子半径与金属半径
- 原子半径（Rahm）
- 206 pm
- 金属半径（C12）
- 91 pm
编号标度
- Mendeleev
- 107
- Pettifor
- 99
- Glawe
- 101
电负性标度
- Ghosh
- 0
- Gunnarsson–Lundqvist
- 9
- Robles–Bartolotti
- 8
极化率与色散
- 偶极极化率
- 14.6 a.u.
- 偶极极化率（不确定度）
- 0.1 a.u.
- C₆
- 94.6 Ha·Bohr6
- C₆ (Gould–Bučko)
- 97.1 Ha·Bohr6
化学亲和力
- 质子亲和能
- 513.6 kJ/mol
- 气相碱性
- 490.1 kJ/mol
供应风险与经济性
- 生产集中度
- 24
- 相对供应风险
- 4
- 政治稳定性（最大生产国）
- 24
相变与同素异形体
| 熔点 | 171.65 K |
| 沸点 | 239.11 K |
| 临界点（温度） | 417.05 K |
| 临界点（压力） | 7.99 MPa |
氧化态分类
高级参考数据
屏蔽常数 (5)
| n | 轨道 | σ |
|---|---|---|
| 1 | s | 0.4761 |
| 2 | p | 4.0068 |
| 2 | s | 5.5696 |
| 3 | p | 10.8839 |
| 3 | s | 9.9317 |
晶体半径详情 (4)
| 电荷 | CN | 自旋 | rcrystal (pm) | 来源 |
|---|---|---|---|---|
| -1 | VI | 167 | Pauling's (1960) crystal radius, | |
| 5 | IIIPY | 26 | ||
| 7 | IV | 22 | ||
| 7 | VI | 41 | Ahrens (1952) ionic radius, |
同位素衰变方式 (45)
| 同位素 | 模式 | 强度 |
|---|---|---|
| 28 | p | 100% |
| 29 | p | 100% |
| 30 | p | 100% |
| 31 | B+ | 100% |
| 31 | B+p | 2.4% |
| 32 | B+ | 100% |
| 32 | B+A | 0.1% |
| 32 | B+p | 0% |
| 33 | B+ | 100% |
| 34 | B+ | 100% |
X射线散射因子 (504)
| 能量 (eV) | f₁ | f₂ |
|---|---|---|
| 10 | — | 1.46938 |
| 10.1617 | — | 1.6922 |
| 10.3261 | — | 1.9488 |
| 10.4931 | — | 2.24432 |
| 10.6628 | — | 2.51303 |
| 10.8353 | — | 2.73153 |
| 11.0106 | — | 2.95549 |
| 11.1886 | — | 3.19416 |
| 11.3696 | — | 3.48881 |
| 11.5535 | — | 3.87618 |
补充数据
Estimated Crustal Abundance
The estimated element abundance in the earth's crust.
1.45×102 milligrams per kilogram
参考文献 (1)
- [5] Chlorine https://education.jlab.org/itselemental/ele017.html
Estimated Oceanic Abundance
The estimated element abundance in the earth's oceans.
1.94×104 milligrams per liter
参考文献 (1)
- [5] Chlorine https://education.jlab.org/itselemental/ele017.html
Sources
Sources of this element.
In nature it is found in the combined state only, chiefly with sodium as common salt (NaCl), carnallite, and sylvite.
参考文献 (1)
- [6] Chlorine https://periodic.lanl.gov/17.shtml
Isotopes in Forensic Science and Anthropology
Information on the use of this element's isotopes in forensic science and anthropology.
Analyses of chlorine isotopes and other environmental tracers can help to identify whether an environmental contaminant is of anthropogenic origin or naturally occurring. For example, perchlorate (ClO4 -) can be of anthropogenic origin and is also found naturally. Perchlorate is a widespread groundwater contaminant that can interfere with hormone production in the thyroid gland by displacing iodide. Both the stable chlorine isotope-amount ratio n(37Cl)/n(35Cl) and the mole fraction of 36Cl, n(36Cl)/n(Cl), can provide useful information about origins of perchlorate in the environment (Fig. IUPAC.17.2). Such information may be important for legal reasons and for remediation of contaminated areas [152] M. A. Stewart, A. J. Spivack. Rev. Mineral. Geochem.55, 231 (2004)., [153] J. K. Böhlke, N. C. Sturchio, B. Gu, J. Horita, G. M. Brown, W. A. Jackson, J. R. Batista, P. B. Hatzinger. Anal. Chem.77, 7838 (2005)..
参考文献 (4)
- [152] M. A. Stewart, A. J. Spivack. Rev. Mineral. Geochem.55, 231 (2004).
- [153] J. K. Böhlke, N. C. Sturchio, B. Gu, J. Horita, G. M. Brown, W. A. Jackson, J. R. Batista, P. B. Hatzinger. Anal. Chem.77, 7838 (2005).
- [154] J. K. Böhlke, P. Hatzinger, N. C. Sturchio, B. Gu, I. J. Abbene, S. J. Mroczkowski. Environ. Sci. Technol.43, 5619 (2009).
- [4] IUPAC Periodic Table of the Elements and Isotopes (IPTEI) https://doi.org/10.1515/pac-2015-0703
参考文献
(9)
Data deposited in or computed by PubChem
The half-life and atomic mass data was provided by the Atomic Mass Data Center at the International Atomic Energy Agency.
Element data are cited from the Atomic weights of the elements (an IUPAC Technical Report). The IUPAC periodic table of elements can be found at https://iupac.org/what-we-do/periodic-table-of-elements/. Additional information can be found within IUPAC publication doi:10.1515/pac-2015-0703 Copyright © 2020 International Union of Pure and Applied Chemistry.
The information are cited from Pure Appl. Chem. 2018; 90(12): 1833-2092, https://doi.org/10.1515/pac-2015-0703.
Thomas Jefferson National Accelerator Facility (Jefferson Lab) is one of 17 national laboratories funded by the U.S. Department of Energy. The lab's primary mission is to conduct basic research of the atom's nucleus using the lab's unique particle accelerator, known as the Continuous Electron Beam Accelerator Facility (CEBAF). For more information visit https://www.jlab.org/
The periodic table at the LANL (Los Alamos National Laboratory) contains basic element information together with the history, source, properties, use, handling and more. The provenance data may be found from the link under the source name.
The periodic table contains NIST's critically-evaluated data on atomic properties of the elements. The provenance data that include data for atomic spectroscopy, X-ray and gamma ray, radiation dosimetry, nuclear physics, and condensed matter physics may be found from the link under the source name. Ref: https://www.nist.gov/pml/atomic-spectra-database
This section provides all form of data related to element Chlorine.
The element property data was retrieved from publications.