Arsenic trisulfide
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| Names | |
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| Preferred IUPAC name Arsenic trisulfide | |
Other names
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| Identifiers | |
3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.013.744 |
| EC Number |
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PubChem CID | |
| RTECS number |
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| UNII | |
CompTox Dashboard (EPA) | |
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| Properties | |
| As2S3 | |
| Molar mass | 246.02 g·mol−1 |
| Appearance | yellow or orange crystals |
| Density | 3.43 g/cm3 |
| Melting point | 310 °C (590 °F; 583 K) |
| Boiling point | 707 °C (1,305 °F; 980 K) |
| insoluble | |
| Solubility | soluble in ammonia |
| −70.0·10−6 cm3/mol | |
| Structure[1] | |
| monoclinic | |
| P21/n (No. 11) | |
a = 1147.5(5) pm, b = 957.7(4) pm, c = 425.6(2) pm α = 90°, β = 90.68(8)°, γ = 90° | |
| pyramidal (As) | |
| Hazards | |
| GHS labelling:[3][4] | |
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| Danger | |
| H300, H331, H400, H411 | |
| NFPA 704 (fire diamond) | |
| NIOSH (US health exposure limits): | |
PEL (Permissible) | [1910.1018] TWA 0.010 mg/m3[2] |
REL (Recommended) | Ca C 0.002 mg/m3 [15-minute][2] |
IDLH (Immediate danger) | Ca [5 mg/m3 (as As)][2] |
| Related compounds | |
Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Arsenic trisulfide is the inorganic compound with the formula As2S3. It is a dark yellow solid that is insoluble in water. It also occurs as the mineral orpiment (Latin: auripigmentum), which has been used as a pigment called King's yellow. It is produced in the analysis of arsenic compounds. It is a group V/VI, intrinsic p-type semiconductor and exhibits photo-induced phase-change properties.[clarification needed]
Structure
[edit]As2S3 occurs both in crystalline and amorphous forms. Both forms feature polymeric structures consisting of trigonal pyramidal As(III) centres linked by sulfide centres. The sulfide centres are two-fold coordinated to two arsenic atoms. In the crystalline form, the compound adopts a ruffled sheet structure.[5] The bonding between the sheets consists of van der Waals forces. The crystalline form is usually found in geological samples. Amorphous As2S3 does not possess a layered structure but is more highly cross-linked. Like other glasses, there is no medium or long-range order, but the first co-ordination sphere is well defined. As2S3 is a good glass former and exhibits a wide glass-forming region in its phase diagram.
Properties
[edit]It is a semiconductor, with a direct band gap of 2.7 eV.[6] The wide band gap makes it transparent to infrared light between 620 nm and 11 μm.
Synthesis
[edit]From the elements
[edit]Amorphous As2S3 is obtained via the fusion of the elements at 390 °C. Rapid cooling of the reaction melt gives a glass. The reaction can be represented with the chemical equation:
- 2 As + 3 S → As2S3
Aqueous precipitation
[edit]As2S3 forms when aqueous solutions containing As(III) are treated with H2S. Arsenic was in the past analyzed and assayed by this reaction, which results in the precipitation of As2S3, which is then weighed. As2S3 can even be precipitated in 6 M HCl. As2S3 is so insoluble that it is not toxic.
Reactions
[edit]Upon heating in a vacuum, polymeric As2S3 "cracks" to give a mixture of molecular species, including molecular As4S6.[7][8] As4S6 adopts the adamantane geometry, like that observed for P4O6 and As4O6. When a film of this material is exposed to an external energy source such as thermal energy (via thermal annealing [9]), electromagnetic radiation (i.e. UV lamps, lasers,[10] electron beams)[11]), As4S6 polymerizes:
- 2 (As2S3)n ⇌ n As4S6
As2S3 characteristically dissolves upon treatment with aqueous solutions containing sulfide ions.[clarification needed] The dissolved arsenic species is the pyramidal trithioarsenite anion AsS3−3:
- As2S3 + 6 NaSH → 2 AsS3−3 + 3 H2S[clarification needed]
As2S3 is the anhydride of the hypothetical trithioarsenous acid, As(SH)3. Upon treatment with polysulfide ions, As2S3 dissolves to give a variety of species containing both S–S and As–S bonds. One derivative is S7As−S−, an eight-membered ring that contains 7 S atoms and 1 As atom, and an exocyclic sulfido center attached to the As atom. As2S3 also dissolves in strongly alkaline solutions to give a mixture of AsS3−3 and AsO3−3.[12]
"Roasting" As2S3 in air gives volatile, toxic derivatives, this conversion being one of the hazards associated with the refining of heavy metal ores:
- 2 As2S3 + 9 O2 → As4O6 + 6 SO2
Contemporary uses
[edit]As an inorganic photoresist
[edit]Due to its high refractive index of 2.45 and its large Knoop hardness compared to organic photoresists, As2S3 has been investigated for the fabrication of photonic crystals with a full-photonic band-gap. Advances in laser patterning techniques such as three-dimensional direct laser writing (3-D DLW) and chemical wet-etching chemistry, has allowed this material to be used as a photoresist to fabricate 3-D nanostructures.[13][14]
As2S3 has been investigated for use as a high resolution photoresist material since the early 1970s,[15][16] using aqueous etchants. Although these aqueous etchants allowed for low-aspect ratio 2-D structures to be fabricated, they do not allow for the etching of high aspect ratio structures with 3-D periodicity. Certain organic reagents, used in organic solvents, permit the high-etch selectivity required to produce high-aspect ratio structures with 3-D periodicity.
Medical applications
[edit]As2S3 and As4S4 have been investigated as treatments for acute promyelocytic leukemia (APL).
For IR-transmitting glasses
[edit]Arsenic trisulfide manufactured into amorphous form is used as a chalcogenide glass for infrared optics. It is transparent for light between wavelengths of 620 nm and 11 μm. The arsenic trisulfide glass is more resistant to oxidation than crystalline arsenic trisulfide, which minimizes toxicity concerns.[17] It can be also used as an acousto-optic material.
Arsenic trisulfide was used for the distinctive eight-sided conical nose over the infra-red seeker of the de Havilland Firestreak missile.
Role in ancient artistry
[edit]The ancient Egyptians reportedly used orpiment, natural or synthetic, as a pigment in artistry and cosmetics.
Miscellaneous
[edit]Arsenic trisulfide is also used as a tanning agent. It was formerly used with indigo dye for the production of pencil blue, which allowed dark blue hues to be added to fabric via pencil or brush.
Precipitation of arsenic trisulfide is used as an analytical test for presence of dissimilatory arsenic-reducing bacteria (DARB).[18]
Safety
[edit]As2S3 is so insoluble that its toxicity is low. Aged samples can contain substantial amounts of arsenic oxides, which are soluble and therefore highly toxic.
Natural occurrence
[edit]Orpiment is found in volcanic environments, often together with other arsenic sulfides, mainly realgar. It is sometimes found in low-temperature hydrothermal veins, together with some other sulfide and sulfosalt minerals.
References
[edit]- ^ Mullen, D. J. E.; Nowacki, W (1972), "Refinement of the crystal structures of realgar, AsS and orpiment, As2S3" (PDF), Z. Kristallogr., 136 (1–2): 48–65, Bibcode:1972ZK....136...48M, doi:10.1524/zkri.1972.136.1-2.48.
- ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0038". National Institute for Occupational Safety and Health (NIOSH).
- ^ Index no. 033-002-00-5 of Annex VI, Part 3, to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) No 1907/2006. OJEU L353, 31.12.2008, pp 1–1355 at p 427.
- ^ "Arsenic, inorganic compounds (as As)", 29 C.F.R. § 1910.1018, 58 FR 35310, June 30, 1993, as amended. "Arsenic (inorganic compounds, as As)", Pocket Guide to Chemical Hazards, U.S. Department of Health and Human Services (NIOSH) Publication No. 2005-149, Washington, DC: Government Printing Office, 2005, ISBN 9780160727511.
- ^ Wells, A.F. (1984). Structural Inorganic Chemistry, Oxford: Clarendon Press. ISBN 0-19-855370-6.
- ^ Arsenic sulfide (As2S3)
- ^ Martin, T.P. (1983). "Arsenic sulfide clusters". Solid State Communications. 47 (2). Elsevier BV: 111–114. Bibcode:1983SSCom..47..111M. doi:10.1016/0038-1098(83)90620-8. ISSN 0038-1098.
- ^ Hammam, M.; Santiago, J.J. (1986). "Evidence for As4S6 molecule as a structural model for amorphous arsenic sulfide from mass spectrometric analysis". Solid State Communications. 59 (11). Elsevier BV: 725–727. Bibcode:1986SSCom..59..725H. doi:10.1016/0038-1098(86)90705-2. ISSN 0038-1098.
- ^ Street, R. A.; Nemanich, R. J.; Connell, G. A. N. (1978-12-15). "Thermally induced effects in evaporated chalcogenide films. II. Optical absorption". Physical Review B. 18 (12). American Physical Society (APS): 6915–6919. Bibcode:1978PhRvB..18.6915S. doi:10.1103/physrevb.18.6915. ISSN 0163-1829.
- ^ Zoubir, Arnaud; Richardson, Martin; Rivero, Clara; Schulte, Alfons; Lopez, Cedric; et al. (2004-04-01). "Direct femtosecond laser writing of waveguides in As2S3 thin films". Optics Letters. 29 (7). The Optical Society: 748–50. Bibcode:2004OptL...29..748Z. doi:10.1364/ol.29.000748. ISSN 0146-9592. PMID 15072379.
- ^ Nordman, Olli; Nordman, Nina; Peyghambarian, Nasser (1998). "Electron beam induced changes in the refractive index and film thickness of amorphous AsxS100−x and AsxSe100−x films". Journal of Applied Physics. 84 (11). AIP Publishing: 6055–6058. doi:10.1063/1.368915. ISSN 0021-8979.
- ^ Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5.
- ^ Wong, S.; Deubel, M.; Pérez-Willard, F.; John, S.; Ozin, G. A.; Wegener, M.; von Freymann, G. (2006-02-03). "Direct Laser Writing of Three- Dimensional Photonic Crystals with a Complete Photonic Bandgap in Chalcogenide Glasses". Advanced Materials. 18 (3). Wiley: 265–269. Bibcode:2006AdM....18..265W. doi:10.1002/adma.200501973. ISSN 0935-9648. S2CID 53527218.
- ^ Wong, Sean H.; Thiel, Michael; Brodersen, Peter; Fenske, Dieter; Ozin, Geoffrey A.; Wegener, Martin; von Freymann, Georg (2007). "Highly Selective Wet Etch for High-Resolution Three-Dimensional Nanostructures in Arsenic Sulfide All-Inorganic Photoresist". Chemistry of Materials. 19 (17). American Chemical Society (ACS): 4213–4221. doi:10.1021/cm070756y. ISSN 0897-4756.
- ^ Stoycheva, Rumiana; Simidchieva, Penka; Buroff, Atanas (1987). "Temperature dependence of the photodissociation of a-As2S3". Journal of Non-Crystalline Solids. 90 (1–3). Elsevier BV: 541–544. doi:10.1016/s0022-3093(87)80482-9. ISSN 0022-3093.
- ^ Zenkin, S. A.; Mamedov, S. B.; Mikhailov, M. D.; Turkina, E. Yu.; Yusupov, I. Yu. Glass Phys. Chem. 1997, 5, pp 393-399.
- ^ Material Safety Data Sheet Archived October 7, 2007, at the Wayback Machine
- ^ Linping Kuai, Arjun A. Nair, and Martin F. Polz "Rapid and Simple Method for the Most-Probable-Number Estimation of Arsenic-Reducing Bacteria" Appl Environ Microbiol. 2001, vol. 67, 3168–3173. doi:10.1128/AEM.67.7.3168-3173.2001.
Further reading
[edit]- "Arsenic and arsenic compounds", Overall Evaluations of Carcinogenicity: An Updating of IARC Monographs Volumes 1 to 42 (PDF), IARC Monographs on the Evaluation of Carcinogenic Risks to Humans Supplement 7, Lyon, France: International Agency for Research on Cancer, 1987, pp. 100–6, ISBN 92-832-1411-0. "Arsenic in Drinking Water", Some Drinking-water Disinfectants and Contaminants, including Arsenic (PDF), IARC Monographs on the Evaluation of Carcinogenic Risks to Humans 84, Lyon, France: International Agency for Research on Cancer, 2004, pp. 39–267, ISBN 92-832-1284-3.
- "Arsenic Compounds, Inorganic", Report on Carcinogens, Eleventh Edition (PDF), U.S. Department of Health and Human Services, Public Health Service, National Toxicology Program, 2005.