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{{Chembox
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| verifiedrevid = 441677973
| ImageFile = Holmium%28III%29_oxide.jpg
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| IUPACName = Holmium(III) oxide
| OtherNames = Holmium oxide, Holmia
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| UNII_Ref = {{fdacite|correct|FDA}}
| PubChem = 4232365▼
| UNII = 6A1MAM6A4J
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| SMILES = [O][Ho]O[Ho][O]▼
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| ExactMass = 377.845382204 g mol<sup>-1</sup>▼
▲| Density = 8.41 g cm<sup>-3</sup>
▲| Appearance = Pale yellow, opaque crystals
▲| MeltingPtC = 2415
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▲| BoilingPtC = 3900
▲| BandGap = 5.3 eV <ref name=optics/>
|Section3={{Chembox Structure
▲| RefractIndex = 1.8 <ref name=optics>{{cite journal|doi=10.1016/S0040-6090(01)01760-6|title=Preparation and optical properties of holmium oxide thin films|year=2002|author=Wiktorczyk, T|journal=Thin Solid Films|volume=405|pages=238|bibcode=2002TSF...405..238W}}</ref>
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▲| CrystalStruct = Cubic, cI80
▲| SpaceGroup = Ia-3, No. 206
| HeatCapacity = 115.0 J mol<sup>−1</sup> K<sup>−1</sup>
}}
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| GHSPictograms = {{GHS07}}{{GHS09}}
▲| Entropy = 158.2 J mol<sup>-1</sup> K<sup>-1</sup>
| GHSSignalWord = Warning
▲| HeatCapacity = 115.0 J mol<sup>-1</sup> K<sup>-1</sup>
| HPhrases = {{H-phrases|319|410}}
| PPhrases = {{P-phrases|264|273|280|305+351+338|337+313|391|501}}
▲| ExternalMSDS = [http://www.espimetals.com/msds%27s/holmiumoxide.pdf External MSDS]
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| OtherCations = [[Dysprosium(III) oxide]]<br>[[Erbium(III) oxide]]
| OtherCompounds = [[Bismuth(III) oxide]]<br />
[[Europium(III) oxide]]<br />
[[Gold(III) oxide]]<br />
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'''Holmium(III) oxide''', or '''holmium oxide''' is a [[chemical compound]] of
==Properties==
===Appearance===
Holmium oxide has some fairly dramatic color changes depending on the lighting conditions. In daylight, it is a tannish yellow color. Under trichromatic light, it is a fiery orange red, almost indistinguishable from the way erbium oxide looks under this same lighting. This is related to the sharp emission bands of the phosphors.<ref name=su/> Holmium oxide has a wide [[band gap]] of 5.3 eV<ref name=optics/> and thus should appear colorless. The yellow color originates from abundant lattice defects (such as oxygen vacancies) and is related to internal transitions at the Ho<sup>3+</sup> ions.<ref name=su>{{cite journal| doi=10.1246/cl.2008.762| title=Hydrothermal Synthesis of GdVO4:Ho3+ Nanorods with a Novel White-light Emission| year=2008| author=Su, Yiguo| journal=Chemistry Letters| volume=37| pages=762| last2=Li| first2=Guangshe| last3=Chen| first3=Xiaobo| last4=Liu| first4=Junjie| last5=Li| first5=Liping| issue=7}}</ref>
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===Crystalline structure===
[[File:Tl2O3structure.jpg|thumb|left|Room-temperature structure of Ho<sub>2</sub>O<sub>3</sub> viewed along a cubic axis. Red atoms are oxygens]]
[[File:Holmium oxide lamellar particles.png|left|thumb|[[Electron micrograph]] of lamellar particles and aggregates of holmium oxide. Scale bar at bottom shows 10 [[Micrometre|μm]].]]
Holmium oxide has a [[cubic crystal system|cubic]], yet rather complex [[bixbyite]] structure, with many atoms per unit cell and a large lattice constant of 1.06 nm. This structure is characteristic of oxides of heavy rare-earth elements, such as Tb<sub>2</sub>O<sub>3</sub>, Dy<sub>2</sub>O<sub>3</sub>, Er<sub>2</sub>O<sub>3</sub>, Tm<sub>2</sub>O<sub>3</sub>, Yb<sub>2</sub>O<sub>3</sub> and Lu<sub>2</sub>O<sub>3</sub>. The thermal expansion coefficient of Ho<sub>2</sub>O<sub>3</sub> is also relatively large at 7.4
===Chemical===
Treating holmium oxide with [[hydrogen chloride]] or with [[ammonium chloride]] affords the corresponding [[holmium(III) chloride|holmium chloride]]:<ref name=patnaik/>
:Ho<sub>2</sub>O<sub>3</sub> + 6 NH<sub>4</sub>Cl → 2 HoCl<sub>3</sub> + 6 NH<sub>3</sub> + 3 H<sub>2</sub>O
Holmium(III) oxide can also react with [[hydrogen sulfide]] to form [[holmium(III) sulfide]] at high temperatures.<ref>{{Cite book|editor1=G. Meyer |editor2= Lester R. Morss |title=Synthesis of Lanthanide and Actinide Compounds |publisher=Kluwer Academic Publishers |year=1991 |at=pp. 329–335 |isbn=0792310187 |url=https://books.google.com/books?id=bnS5elHL2w8C&pg=PA329|access-date=18 August 2022}}</ref>
==History==
Holmium (''Holmia'', [[Latin]] name for [[Stockholm]]) was [[discovery of the chemical elements|discovered]] by [[Marc Delafontaine]] and [[Jacques-Louis Soret]] in 1878 who noticed the aberrant [[Spectrophotometry|spectrographic]] [[absorption band]]s of the then-unknown element (they called it "Element X").<ref>{{cite journal|title = Sur les spectres d'absorption ultra-violets des terres de la gadolinite|author = Jacques-Louis Soret|journal = Comptes rendus de l'Académie des sciences|volume = 87|pages = 1062|year = 1878|url = http://gallica.bnf.fr/ark:/12148/bpt6k3043m/f1124.table}}
</ref><ref>{{cite journal|title = Sur le spectre des terres faisant partie du groupe de l'yttria
| author = Jacques-Louis Soret|journal = Comptes rendus de l'Académie des sciences
| volume = 89|pages = 521|year = 1879|url =
</ref> Later in 1878, [[Per Teodor Cleve]] independently discovered the element while he was working on [[erbia]] earth ([[Erbium(III) oxide|erbium oxide]]).<ref>{{cite journal
| title = Sur deux nouveaux éléments dans l'erbine|author =
▲|year = 1879|url = http://gallica.bnf.fr/ark:/12148/bpt6k3046j/f432.table}}
</ref><ref>{{cite journal|title = Sur l'erbine|author = Per Teodor Cleve
| journal = Comptes rendus de l'Académie des sciences|volume = 89|pages = 708|year = 1879
| url = http://gallica.bnf.fr/ark:/12148/bpt6k3046j/f759.table}}</ref>
Using the method developed by [[Carl Gustaf Mosander]], Cleve first removed all of the known contaminants from erbia. The result of that effort was two new materials, one brown and one green. He named the brown substance holmia (after the Latin name for Cleve's home town, Stockholm) and the green one thulia. Holmia was later found to be the
==Occurrence==
[[File:Gadolinitas.jpg|thumb|Gadolinite contains traces of holmium(III) oxide]]Holmium readily oxidizes in air; therefore presence of holmium in nature is synonymous with that of holmia. Holmium oxide occurs in trace amounts in the minerals [[gadolinite]], [[monazite]], and in other rare-earth [[mineral]]s.
==Production==
A typical extraction process of holmium oxide can be simplified as follows:
The most efficient separation routine for holmium oxide from the rare-earths is [[ion exchange]]. In this process, rare-earth ions are adsorbed onto suitable ion-exchange resin by exchange with hydrogen, ammonium or cupric ions present in the resin. The rare earth ions are then selectively washed out by suitable complexing agent, such as ammonium citrate or
==Applications==
[[File:HoOxideSolution.jpg|thumb|A solution of 4% holmium oxide in 10% perchloric acid, permanently fused into a quartz cuvette as an optical calibration standard]]
Holmium oxide is one of the colorants used for [[cubic zirconia]] and [[glass]], providing yellow or red coloring.<ref>{{cite web|
==Health effects==
[[File:Holmium 166m oxide.png|thumb|Holmium-166m oxide, an [[isotopologue]]]]
Holmium(III) oxide is, compared to many other compounds, not very dangerous, although repeated overexposure can cause [[granuloma]] and [[hemoglobinemia]]. It has low oral, dermal and inhalation toxicities and is non-irritating. The acute oral [[median lethal dose]] (LD<sub>50</sub>) is greater than 1 g per kilogram of body weight.<ref>{{cite web|
== References ==
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{{Holmium compounds}}
{{Oxides}}
{{oxygen compounds}}
[[Category:Holmium compounds]]
[[Category:Sesquioxides]]
[[Category:Crystals in space group 206]]
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