Hafnium (Hf)
transition-metalSolid
標準原子量
178.49 u電子配置
[Xe] 6s2 4f14 5d2融点
2232.85 °C沸点
4602.85 °C密度
1.33e+4 kg/m³酸化数
−2, 0, +1, +2, +3, +4電気陰性度（Pauling）
1.3第1イオン化エネルギー
6.82507 eV発見年
1911原子半径
155 pm詳細
Hafnium is a dense, corrosion-resistant transition metal in group 4, chemically close to zirconium. It occurs almost entirely with zirconium minerals and is difficult to separate because the two elements have similar ionic sizes and chemistry. A defining technological feature is its very large thermal-neutron absorption cross section, which contrasts with zirconium's low absorption and makes high-purity separation important for nuclear applications.
Hafnium is a ductile metal with a brilliant silver luster. Its properties are considerably influenced by presence of zirconium impurities. Of all the elements, zirconium and hafnium are two of the most difficult to separate. Although their chemistry is almost identical, the density of zirconium is about half of hafnium. Very pure hafnium has been produced, with zirconium being the major impurity.
Hafnium has been successfully alloyed with iron, titanium, niobium, tantalum, and other metals. Hafnium carbide is the most refractory binary composition known, and the nitride is the most refractory of all known metal nitrides (m.p. 3310C). At 700 degrees C hafnium rapidly absorbs hydrogen to form the composition HfH1.86.
Hafnium is resistant to concentrated alkalis, but at elevated temperatures reacts with oxygen, nitrogen, carbon, boron, sulfur, and silicon. Halogens react directly to form tetrahalides.
The name derives from the Latin hafnia for Copenhagen. An element named celtium was erroneously claimed to have been discovered in 1911 by the French chemist Georges Urbain in rare earth samples, until the Danish physicist Niels Bohr, predicted hafnium's properties using his theory of electronic configuration of the elements. Bohr argued that hafnium would not be a rare earth element, but would be found in zirconium ore. Hafnium was discovered by the Dutch physicist Dirk Coster and the Hungarian physicist George von Hevesy in 1923, while working at Bohr's Institute in Copenhagen.
Hafnium was discovered by Dirk Coster, a Danish chemist, and George Charles de Hevesy, a Hungarian chemist, in 1923. They used a method known as X-ray spectroscopy to study the arrangement of the outer electrons of atoms in samples of zirconium ore. The electron structure of hafnium had been predicted by Niels Bohr and Coster and Hevesy found a pattern that matched. Hafnium is difficult to separate from zirconium and is present in all of its ores. It is obtained with the same methods used to extract zirconium.
From Hafinia, the Latin name for Copenhagen. Many years before its discovery in 1923 (credited to D. Coster and G. von Hevesey), Hafnium was thought to be present in various minerals and concentrations. On the basis of the Bohr theory, the new element was expected to be associated with zirconium.
It was finally identified in zircon from Norway, by means of X-ray spectroscope analysis. It was named in honor of the city in which the discovery was made. Most zirconium minerals contain 1 to 5 percent hafnium.
It was originally separated from zirconium by repeated recrystallization of the double ammonium or potassium fluorides by von Hevesey and Jantzen. Metallic hafnium was first prepared by van Arkel and deBoer by passing the vapor of the tetraiodide over a heated tungsten filament. Almost all hafnium metal now produced is made by reducing the tetrachloride with magnesium or with sodium (Kroll Process).
Pure hafnium is a lustrous, silvery-gray metal. It is solid and ductile under ordinary conditions and develops a thin protective oxide film in air. Finely divided hafnium can be much more reactive than bulk metal.
Hafnium is used chiefly where neutron absorption or high-temperature stability is valuable. Metallic hafnium is used in control rods and other neutron-absorbing components in some nuclear reactors. Hafnium-containing superalloys and refractory alloys can improve high-temperature strength and oxidation resistance. Hafnium dioxide, HfO₂, is used as a high-k dielectric material in semiconductor devices, replacing or supplementing silicon dioxide in advanced gate stacks. Hafnium compounds also appear in specialty ceramics, optical coatings, and catalysts, but these uses are smaller than zirconium-related industrial chemistry.
Hafnium is a good absorber of neutrons and is used in the control rods of nuclear reactors. Hafnium is also used in vacuum tubes as a getter, a material that combines with and removes trace gases from vacuum tubes. Hafnium has been used as an alloying agent in iron, titanium, niobium and other metals.
Melting near 3890°C, hafnium carbide (HfC) has the highest melting point of any known two-element compound. Hafnium nitride (HfN) also has a high melting point, around 3305°C. Other hafnium compounds include: hafnium chloride (HfCl4), hafnium fluoride (HfF4) and hafnium oxide (HfO2).
Because the element not only has a good absorption cross section for thermal neutrons (almost 600 times that of zirconium), but also excellent mechanical properties and is extremely corrosion-resistant, hafnium is used for reactor control rods. Such rods are used in nuclear submarines.
Hafnium is used in gas-filled and incandescent lamps, and is an efficient getter for scavenging oxygen and nitrogen.
Isotopes in Geochronology
Some 176Hf is radiogenic as a result of it being formed as a product of beta decay of radioactive 176Lu (half-life of 3.73×1010 years) [301] G. Faure. Principles of Isotope Geology, 2nd Edition. p. 608. Wiley, New York (1986).. Thus, relations between the isotope-amount ratiosn(176Hf)/n(177Hf) and n(176Hf)/n(176Lu) have been used to determine the ages of minerals and rocks. Because of the long half-life of 176Lu, these ratios have been used in geochronology studies that document some of the oldest rocks in the Solar System and on Earth (Fig. IUPAC.72.1).
Hafnium isotopic compositions of terrestrial materials evolved differently depending on the relative rates of 176Hf production. Geologists can use calculated lutetium-hafnium ages and the initial isotope-amount ratio n(176Hf)/n(177Hf) along with other isotopic data from the oldest rocks in the Earth to infer that the Earth’s crust differentiated within the first few hundred million years after condensation of the oldest solid matter in the Solar System [502] E. Scherer, C. Münker, K. Mezger. Science293, 683 (2001)..
Radioactive 182Hf decays to 182W with a half-life of 8.9×106 years, which is much less than the age of meteorites and the Earth. Therefore, measurements of the amounts of hafnium and tungsten isotopes in meteorites and terrestrial samples reveal the earlier presence of 182Hf. As a result, this provides information about chemical differentiation and evolution of the early Solar System [503] T. Kleine, M. Touboul, B. Bourdon, F. Nimmo, K. Mezger, H. Palme, S. B. Jacobsen, Q. Z. Yin, A. N. Halliday. Geochim. Cosmochim. Acta73, 5150 (2009)., [504] A. Schersten. Re-Os, Pt-Os and Hf-W Isotopes and Tracing the Core in Mantle Melts, MantlePlumes.org (2014), Feb. 25; http://www.mantleplumes.org/Os-W.html..
Hafnium chemistry is dominated by the +4 oxidation state, reflecting the stable Hf⁴⁺ ion and strong bonding to oxygen, halides, and other hard donor atoms. Hafnium dioxide, HfO₂, is a refractory, chemically durable oxide with high dielectric constant. Hafnium tetrachloride, HfCl₄, is a volatile moisture-sensitive chloride used in purification and chemical vapor or atomic layer deposition chemistry. Organometallic and amide precursors such as tetrakis(dimethylamido)hafnium, Hf[N(CH₃)₂]₄, are important for thin-film deposition. Lower oxidation states exist but are less common and often require specialized conditions.
See more information at the Hafnium compound page.
Bulk hafnium metal is generally of low acute chemical toxicity, but metal dust or powder can ignite and should be treated as a combustible solid. Hafnium compounds vary in hazard; soluble salts, halides, and organometallic precursors may be corrosive, moisture-sensitive, or toxic by inhalation or skin contact. Hafnium is not naturally radioactive in ordinary material, but reactor-exposed hafnium may contain activation products that require radiological control.
Finely divided hafnium is pyrophoric and can ignite spontaneously in air. Care should be taken when machining the metal or when handling hot sponge hafnium.
Hafnium is a trace lithophile element and follows zirconium in igneous rocks, sands, and resistant minerals. It is commonly hosted in zircon, ZrSiO₄, where hafnium substitutes for zirconium. The element has low mobility in most surface environments because its oxides and silicate-hosted forms are sparingly soluble. It has no known biological role, and environmental concentrations are normally controlled by the distribution and weathering resistance of zirconium minerals.
Hafnium is not usually mined as a primary product. It is recovered during the processing of zirconium minerals, especially when nuclear-grade zirconium is purified to remove neutron-absorbing impurities. Separation from zirconium is the central cost and supply constraint, commonly involving solvent extraction or related chemical fractionation followed by conversion to metal or compounds. Demand is concentrated in nuclear control materials, semiconductor precursors, and specialized high-temperature alloys. Supply is therefore tied to zirconium processing capacity and to the need for very low-hafnium zirconium in reactor fuel cladding, rather than to abundant independent hafnium ores.
Obtained from mineral zircon or baddeleyite.
Hafnium is a heavy element made mainly by neutron-capture processes in earlier generations of stars, with contributions from both slow and rapid neutron capture. It is far less abundant cosmically than lighter rock-forming elements. In planetary materials it behaves as a refractory lithophile element, condensing into high-temperature solids and concentrating with zirconium-bearing minerals rather than in metallic cores or volatile phases.
- Hafnium was one of the last stable elements to be identified in nature.
- Its name comes from Hafnia, the Latin name for Copenhagen.
- Zircon can contain enough hafnium to make separation important even when hafnium is not the desired product.
- Hafnium and zirconium are chemically so similar that early analytical work often missed hafnium.
- Hafnium carbide and tantalum hafnium carbide are noted for extremely high melting behavior.
画像
性質
物理的性質
- 原子半径（経験値）
- 155 pm 全元素の原子半径（経験値）を比較 →
- 共有結合半径
- 175 pm 全元素の共有結合半径を比較 →
- ファンデルワールス半径
- 212 pm 全元素のファンデルワールス半径を比較 →
- 金属半径
- 144 pm 全元素の金属半径を比較 →
- 密度
- 1.33 × 104 kg/m³ 全元素の密度を比較 →
- モル体積
- 0.0136 L/mol
- 標準温度・圧力（STP）での相
- 固体 全元素の標準温度・圧力（STP）での相を比較 →
- 融点
- 2232.85 °C 全元素の融点を比較 →
- 沸点
- 4602.85 °C 全元素の沸点を比較 →
- 熱伝導率
- 23 W/(m·K) 全元素の熱伝導率を比較 →
- 比熱容量
- 0.144 J/(g·K) 全元素の比熱容量を比較 →
- モル熱容量
- 25.73 J/(mol·K) 全元素のモル熱容量を比較 →
- 結晶構造
- 六方最密充填構造 全元素の結晶構造を比較 →
化学的性質
- 電気陰性度（Pauling）
- 1.3 全元素の電気陰性度（Pauling）を比較 →
- 電気陰性度（Allen）
- 1.16
- 電子親和力
- 0.178 eV
- 第1イオン化エネルギー
- 6.82507 eV 全元素の第1イオン化エネルギーを比較 →
- 第2イオン化エネルギー
- 14.61005 eV 全元素の第2イオン化エネルギーを比較 →
- 第3イオン化エネルギー
- 22.550078 eV 全元素の第3イオン化エネルギーを比較 →
- 第4イオン化エネルギー
- 33.370115 eV 全元素の第4イオン化エネルギーを比較 →
- 第5イオン化エネルギー
- 68.370235 eV 全元素の第5イオン化エネルギーを比較 →
- 酸化数
- −2, 0, +1, +2, +3, +4 全元素の酸化数を比較 →
- 価電子
- 4 全元素の価電子を比較 →
- 電子配置
- [Xe] 6s2 4f14 5d2
熱力学的性質
- 融解熱
- 0.26667358 eV 全元素の融解熱を比較 →
- 蒸発熱
- 5.959476 eV 全元素の蒸発熱を比較 →
- 昇華熱
- 6.436234 eV
- 原子化熱
- 6.436234 eV
- 原子化エンタルピー
- 6.409286 eV
原子核
- 陽子数
- 72 全元素の陽子数を比較 →
- 中性子数
- 108 全元素の中性子数を比較 →
- 既知の同位体
- 38 全元素の既知の同位体を比較 →
- 安定同位体
- 4 全元素の安定同位体を比較 →
- 最も安定な同位体
- Hf-180
- 発見年
- 1911
存在度
- 存在度（地殻）
- 3 mg/kg 全元素の存在度（地殻）を比較 →
- 存在度（海洋）
- 7 × 10−6 mg/L 全元素の存在度（海洋）を比較 →
結晶構造
- 格子定数a
- 320 pm
電子構造
- 各電子殻の電子数
- 2, 8, 18, 32, 10, 2 全元素の各電子殻の電子数を比較 →
識別子
- CAS登録番号
- 7440-58-6 全元素のCAS登録番号を比較 →
- 項記号
- 3F2
- InChI
- InChI=1S/Hf
- InChI Key
- VBJZVLUMGGDVMO-UHFFFAOYSA-N
電子配置 測定値
Hf: 4f¹⁴ 5d² 6s²[Xe] 4f¹⁴ 5d² 6s²1s² 2s² 2p⁶ 3s² 3p⁶ 3d¹⁰ 4s² 4p⁶ 4d¹⁰ 5s² 5p⁶ 4f¹⁴ 5d² 6s²原子モデル
同位体によって中性子数、質量、安定性は変わりますが、中性原子の電子配置は変わりません。
模式的な原子モデルです。実際の縮尺とは異なります。
原子の指紋
発光／吸収スペクトル
同位体分布
| 質量数 | 原子質量（u） | 天然存在比 | 半減期 |
|---|---|---|---|
| 176 安定 | 175.9414076 ± 0.0000022 | 5.2600% | 安定 |
| 178 安定 | 177.9437058 ± 0.000002 | 27.2800% | 安定 |
| 179 安定 | 178.9458232 ± 0.000002 | 13.6200% | 安定 |
| 180 安定 | 179.946557 ± 0.000002 | 35.0800% | 安定 |
相／状態
理由: 融点（2232.85 °C）より2207.8 °C低い
模式図、実際の縮尺とは異なります
相転移点
相転移エネルギー
融点で1 molを融解させるのに必要なエネルギー
沸点で1 molを蒸発させるのに必要なエネルギー
昇華点で1 molを昇華させるのに必要なエネルギー
密度
標準条件下
標準条件下
原子スペクトル
全72件中10件を表示しています。 イオンの電荷の昇順で並べています。
スペクトル線データの収録状況 ?
| イオン | 電荷 | スペクトル線の総数 | 遷移確率 | 準位の表記 |
|---|---|---|---|---|
| Hf I | 0 | 5341 | 187 | 3821 |
| Hf II | +1 | 218 | 2 | 10 |
| Hf III | +2 | 37 | 0 | 0 |
| Hf IV | +3 | 27 | 0 | 0 |
| Hf V | +4 | 82 | 0 | 0 |
準位データの収録状況 ?
| イオン | 電荷 | 準位 |
|---|---|---|
| Hf I | 0 | 333 |
| Hf II | +1 | 125 |
| Hf III | +2 | 2 |
| Hf IV | +3 | 2 |
| Hf V | +4 | 2 |
| Hf VI | +5 | 2 |
| Hf VII | +6 | 2 |
| Hf VIII | +7 | 2 |
| Hf IX | +8 | 2 |
| Hf X | +9 | 2 |
イオン半径
| 電荷 | 配位 | スピン | 半径 |
|---|---|---|---|
| +4 | 4 | データなし | 57.99999999999999 pm |
| +4 | 6 | データなし | 71 pm |
| +4 | 7 | データなし | 76 pm |
| +4 | 8 | データなし | 83 pm |
化合物
同位体 (4)
| 質量数 | 原子質量（u） | 天然存在比 | 半減期 | 崩壊形式 | |
|---|---|---|---|---|---|
| 176 安定 | 175.9414076 ± 0.0000022 | 5.2600% ± 0.0700% | 安定 | stable | |
| 178 安定 | 177.9437058 ± 0.000002 | 27.2800% ± 0.0700% | 安定 | stable | |
| 179 安定 | 178.9458232 ± 0.000002 | 13.6200% ± 0.0200% | 安定 | stable | |
| 180 安定 | 179.946557 ± 0.000002 | 35.0800% ± 0.1600% | 安定 | stable |
スペクトル線
全1890件中50件を表示しています。 初期設定では、強度の測定値があるスペクトル線のみを表示します。
| 波長（nm） | 強度 | 電離段階 | 種類 | 遷移 | 精度 | 出典 | |
|---|---|---|---|---|---|---|---|
| 417.433998 nm | 48000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5D* | 測定値 | NIST | |
| 380.03629 nm | 36000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5D* | 測定値 | NIST | |
| 382.072307 nm | 34000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p y 3F* | 測定値 | NIST | |
| 723.71003 nm | 34000 | Hf I | emission | 5d2.6s2 a 3F → 5d.6s2.(a 2D).6p z 3D* | 測定値 | NIST | |
| 384.917811 nm | 32000 | Hf I | emission | 5d2.6s2 a 1D → 5d2.(a 3F).6s.(a 2F).6p y 1D* | 測定値 | NIST | |
| 713.1807 nm | 32000 | Hf I | emission | 5d2.6s2 a 3F → 5d.6s2.(a 2D).6p z 3D* | 測定値 | NIST | |
| 389.993003 nm | 29000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5D* | 測定値 | NIST | |
| 395.181289 nm | 26000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p y 3F* | 測定値 | NIST | |
| 385.830632 nm | 25000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p y 3D* | 測定値 | NIST | |
| 724.0873 nm | 21000 | Hf I | emission | 5d2.6s2 a 3F → 5d.6s2.(a 2D).6p z 3D* | 測定値 | NIST | |
| 393.137246 nm | 19000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p y 3D* | 測定値 | NIST | |
| 480.049829 nm | 17000 | Hf I | emission | 5d2.6s2 a 1D → 5d.6s2.(a 2D).6p z 1P* | 測定値 | NIST | |
| 397.347912 nm | 15000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5D* | 測定値 | NIST | |
| 706.38474 nm | 15000 | Hf I | emission | 5d2.6s2 a 1D → 5d.6s2.(a 2D).6p z 3P* | 測定値 | NIST | |
| 381.177553 nm | 14000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 3G* | 測定値 | NIST | |
| 555.06011 nm | 14000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5G* | 測定値 | NIST | |
| 555.211884 nm | 14000 | Hf I | emission | 5d2.6s2 a 1D → 5d.6s2.(a 2D).6p z 1F* | 測定値 | NIST | |
| 456.593715 nm | 13000 | Hf I | emission | 5d2.6s2 a 1D → 5d2.(a 3P).6s.(a 4P).6p y 5D* | 測定値 | NIST | |
| 435.630591 nm | 12000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5D* | 測定値 | NIST | |
| 445.734411 nm | 12000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5F* | 測定値 | NIST | |
| 459.87979 nm | 12000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5F* | 測定値 | NIST | |
| 462.086529 nm | 12000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5F* | 測定値 | NIST | |
| 465.518924 nm | 12000 | Hf I | emission | 5d2.6s2 a 3P → 5d2.(a 3P).6s.(a 4P).6p z 3S* | 測定値 | NIST | |
| 380.044548 nm | 11000 | Hf I | emission | 5d2.6s2 a 1D → 5d2.(a 3P).6s.(a 4P).6p z 5S* | 測定値 | NIST | |
| 429.477692 nm | 11000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5D* | 測定値 | NIST | |
| 681.89395 nm | 11000 | Hf I | emission | 5d2.6s2 a 3P → 5d.6s2.(a 2D).6p z 1F* | 測定値 | NIST | |
| 396.799621 nm | 10000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5D* | 測定値 | NIST | |
| 406.28356 nm | 10000 | Hf I | emission | 5d.6s2.(a 2D).6p z 1D* → 3512 | 測定値 | NIST | |
| 497.525232 nm | 10000 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5F* | 測定値 | NIST | |
| 454.093108 nm | 8400 | Hf I | emission | 5d2.6s2 a 1D → 5d2.(a 3F).6s.(a 4F).6p y 3F* | 測定値 | NIST | |
| 443.80364 nm | 8300 | Hf I | emission | 5d2.6s2 a 3P → 5d2.(a 3P).6s.(a 4P).6p z 3S* | 測定値 | NIST | |
| 446.117576 nm | 8300 | Hf I | emission | 5d2.6s2 a 1D → 5d2.(a 3P).6s.(a 4P).6p z 3S* | 測定値 | NIST | |
| 459.891547 nm | 8300 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5D* | 測定値 | NIST | |
| 408.33549 nm | 8000 | Hf I | emission | 5d.6s2.(a 2D).6p z 1D* → 3499 | 測定値 | NIST | |
| 571.91718 nm | 7300 | Hf I | emission | 5d2.6s2 a 3P → 5d.6s2.(a 2D).6p z 1P* | 測定値 | NIST | |
| 403.225898 nm | 7200 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p y 3F* | 測定値 | NIST | |
| 478.27405 nm | 7100 | Hf I | emission | 5d.6s2.(a 2D).6p z 3F* → 6p2.(3P).5d.(2D).6s c 3D | 測定値 | NIST | |
| 383.001314 nm | 6700 | Hf I | emission | 5d3.(b 4F).6s a 5F → 5d2.(b 1D).6s.(b 2D).6p v 3F* | 測定値 | NIST | |
| 504.743848 nm | 6500 | Hf I | emission | 5d2.6s2 a 3P → 5d2.(a 3F).6s.(a 4F).6p y 3D* | 測定値 | NIST | |
| 485.92338 nm | 6400 | Hf I | emission | 5d.6s2.(a 2D).6p z 3F* → 3512 | 測定値 | NIST | |
| 386.09058 nm | 6300 | Hf I | emission | 5d2.6s2 a 3P → 5d2.(a 3F).6s.(a 2F).6p y 1F* | 測定値 | NIST | |
| 441.790242 nm | 6200 | Hf I | emission | 5d2.6s2 a 1D → 5d2.(a 3F).6s.(a 4F).6p y 3D* | 測定値 | NIST | |
| 388.935622 nm | 5900 | Hf I | emission | 5d2.6s2 a 1D → 5d2.(a 3P).6s.(a 4P).6p y 5D* | 測定値 | NIST | |
| 469.90048 nm | 5900 | Hf I | emission | 5d2.(a 3F).6s.(a 4F).6p z 5G* → 5d2.(3F).6s.(a 4F).7s b 5F | 測定値 | NIST | |
| 678.92714 nm | 5900 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5G* | 測定値 | NIST | |
| 433.027751 nm | 5800 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p y 3F* | 測定値 | NIST | |
| 410.65431 nm | 5600 | Hf I | emission | 5d2.6s2 a 1G → 5d2.(a 3F).6s.(a 2F).6p y 1F* | 測定値 | NIST | |
| 426.34428 nm | 5400 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5F* | 測定値 | NIST | |
| 477.37157 nm | 5400 | Hf I | emission | 5d2.6s2 a 3P → 5d.6s2.(a 2D).6p z 1P* | 測定値 | NIST | |
| 590.29382 nm | 5400 | Hf I | emission | 5d2.6s2 a 3F → 5d2.(a 3F).6s.(a 4F).6p z 5G* | 測定値 | NIST |
詳細な性質
共有結合半径（詳細）
- 共有結合半径（Pyykkö）
- 152 pm
- 共有結合半径（Pyykkö、二重結合）
- 128 pm
- 共有結合半径（Pyykkö、三重結合）
- 122 pm
ファンデルワールス半径
- Batsanov
- 225 pm
- Alvarez
- 263 pm
- UFF
- 314.1 pm
- MM3
- 253 pm
原子半径と金属半径
- 原子半径（Rahm）
- 264 pm
- 金属半径（C12）
- 159 pm
番号付けの尺度
- Mendeleev
- 45
- Pettifor
- 50
- Glawe
- 50
電気陰性度の尺度
- Ghosh
- 0
- Miedema
- 4
- Gunnarsson–Lundqvist
- 5
- Robles–Bartolotti
- 4
分極率と分散
- 双極子分極率
- 103 a.u.
- 双極子分極率（不確かさ）
- 6 a.u.
- C₆ (Gould–Bučko)
- 1040 Ha·Bohr6
ミーデマパラメータ
- ミーデマモル体積
- 13.45 cm3/mol
- ミーデマ電子密度
- 3
相転移と同素体
| 融点 | 2506.15 K |
| 沸点 | 4873.15 K |
酸化数の分類
専門参考データ
遮蔽定数 (14)
| n | 軌道 | σ |
|---|---|---|
| 1 | s | 1.3984 |
| 2 | p | 4.4012 |
| 2 | s | 18.8102 |
| 3 | d | 13.5702 |
| 3 | p | 21.0168 |
| 3 | s | 21.6885 |
| 4 | d | 36.476 |
| 4 | f | 39.7904 |
| 4 | p | 34.0704 |
| 4 | s | 33.0228 |
結晶半径の詳細 (4)
| 電荷 | CN | スピン | rcrystal (pm) | 由来 |
|---|---|---|---|---|
| 4 | IV | 72 | from r^3 vs V plots, | |
| 4 | VI | 85 | from r^3 vs V plots, | |
| 4 | VII | 90 | ||
| 4 | VIII | 97 |
同位体の崩壊形式 (46)
| 同位体 | モード | 強度 |
|---|---|---|
| 153 | B+ | — |
| 154 | B+ | 100% |
| 154 | A | 0% |
| 155 | B+ | 100% |
| 155 | A | — |
| 156 | A | 100% |
| 156 | B+ | — |
| 157 | A | 94% |
| 157 | B+ | 14% |
| 158 | B+ | 55.7% |
X線散乱因子 (514)
| エネルギー (eV) | f₁ | f₂ |
|---|---|---|
| 10 | — | 2.62338 |
| 10.1617 | — | 2.71485 |
| 10.3261 | — | 2.80951 |
| 10.4931 | — | 2.90326 |
| 10.6628 | — | 2.98247 |
| 10.8353 | — | 3.06384 |
| 11.0106 | — | 3.14744 |
| 11.1886 | — | 3.21346 |
| 11.3696 | — | 3.27509 |
| 11.5535 | — | 3.33789 |
追加データ
Estimated Crustal Abundance
The estimated element abundance in the earth's crust.
3.0 milligrams per kilogram
参考文献 (1)
Estimated Oceanic Abundance
The estimated element abundance in the earth's oceans.
7×10-6 milligrams per liter
参考文献 (1)
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 Hafnium.
The element property data was retrieved from publications.