Cadmium iodide

Cadmium iodide
Cadmium iodide
Cadmium iodide
Names
IUPAC name
Cadmium(II) iodide
Other names
Cadmium diiodide
Identifiers
CAS Number
  • 7790-80-9 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 23037 checkY
ECHA InfoCard 100.029.294 Edit this at Wikidata
EC Number
  • 232-223-6
PubChem CID
  • 277692
UNII
  • 2F2UPU4KCW checkY
CompTox Dashboard (EPA)
  • DTXSID20894887 Edit this at Wikidata
InChI
  • InChI=1S/Cd.2HI/h;2*1H/q+2;;/p-2 checkY
    Key: OKIIEJOIXGHUKX-UHFFFAOYSA-L checkY
  • InChI=1/Cd.2HI/h;2*1H/q+2;;/p-2
    Key: OKIIEJOIXGHUKX-NUQVWONBAZ
  • [Cd+2].[I-].[I-]
Properties
Chemical formula
CdI2
Molar mass 366.22 g/mol
Appearance white to pale yellow crystals
Density 5.640 g/cm3, solid
Melting point 387 °C (729 °F; 660 K)
Boiling point 742 °C (1,368 °F; 1,015 K)
Solubility in water
787 g/L (0 °C)
847 g/L (20 °C)
1250 g/L (100 °C)
Solubility soluble in ethanol, acetone, ether and ammonia
-117.2·10−6 cm3/mol
Structure
Trigonal, hP3, space group P3m1, No. 164
octahedral
Hazards
GHS labelling:
GHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard
Danger
H301, H331, H351, H373, H410
P260, P280, P301+P330+P331, P304+P340, P310, P311, P403+P233
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
3
0
0
NIOSH (US health exposure limits):
PEL (Permissible)
[1910.1027] TWA 0.005 mg/m3 (as Cd)[1]
REL (Recommended)
Ca[1]
IDLH (Immediate danger)
Ca [9 mg/m3 (as Cd)][1]
Related compounds
Other anions
cadmium fluoride
cadmium chloride
cadmium bromide
Other cations
zinc iodide
mercury(II) iodide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chemical compound

Cadmium iodide is the inorganic compound with the formula CdI2. It is a white hygroscopic solid. It also can be obtained as a mono- and tetrahydrate.[2] It has few applications. It is notable for its crystal structure, which is typical for compounds of the form MX2 with strong polarization effects.

Preparation

Cadmium iodide is prepared by the addition of cadmium metal, or its oxide, hydroxide or carbonate to hydroiodic acid. Also, the compound can be made by heating cadmium with iodine.[2]

Applications

Historically, cadmium iodide was used as a catalyst for the Henkel process, a high-temperature isomerisation of dipotassium phthalate to yield the terephthalate. The salt was then treated with acetic acid to yield potassium acetate and commercially valuable terephthalic acid.[3]

While uneconomical compared to the production of terephthalic acid from p-xylene, the Henkel method has been proposed as a potential route to produce terephthalic acid from furfural. As existing Bio-PET is still reliant on petroleum as a source of p-xylene, the Henkel process could theoretically offer a completely bioplastic route to polyethylene terephthalate.[4]

Crystal structure

The iodide anions in CdI2 form a hexagonal close-packed lattice, while the cadmium cations occupy all of the octahedral holes in alternating layers.

In cadmium iodide the iodide anions form a hexagonal close packed arrangement while the cadmium cations fill all of the octahedral sites in alternate layers. The resultant structure consists of a layered lattice. This same basic structure is found in many other salts and minerals. Cadmium iodide is mostly ionically bonded but with partial covalent character.[5]

Cadmium iodide's crystal structure is the prototype on which the crystal structures many other compounds can be considered to be based. Compounds with any of the following characteristics tend to adopt the CdI2 structure:[citation needed]

References

  1. ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0087". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ a b F. Wagenknecht; R. Juza (1963). "Cadmium iodide". In G. Brauer (ed.). Handbook of Preparative Inorganic Chemistry, 2nd Ed. Vol. 2. NY, NY: Academic Press. p. 1096.
  3. ^ Solomon, I.; Eisenberg, W. (1976). Utilization of coal conversion process by-products. Quarterly report, December 27, 1975--March 27, 1976 (Report). doi:10.2172/7186862.
  4. ^ Tachibana, Yuya; Kimura, Saori; Kasuya, Ken-Ichi (2015). "Synthesis and Verification of Biobased Terephthalic Acid from Furfural". Scientific Reports. 5: 8249. Bibcode:2015NatSR...5E8249T. doi:10.1038/srep08249. PMC 4316194. PMID 25648201.
  5. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 1211–1212. ISBN 978-0-08-037941-8.
  • v
  • t
  • e
Cadmium(I)
  • Cd2(AlCl4)2
Cadmium(II)
  • Cd(BF4)2
  • CdF2
  • CdCl2
  • CdBr2
  • CdI2
  • Cd(CN)2
  • CdH2
  • CdO
  • CdS
  • CdSe
  • CdTe
  • Cd(OH)2
  • Cd3N2
  • Cd(NO3)2
  • CdSO4
  • CdCrO4
  • CdWO4
  • CdTeO3
  • Cd(C3H5O3)2
  • Cd3As2
  • Cd3P2
  • CsCdCl3
  • CsCdBr3
  • Cd(CH3CO2)2
  • Cd(O2CC17H35)2
  • v
  • t
  • e
Salts and covalent derivatives of the iodide ion
HI
+H
He
LiI BeI2 BI3
+BO3
CI4
+C
NI3
NH4I
+N
I2O4
I2O5
I4O9
IF
IF3
IF5
IF7
Ne
NaI MgI2 AlI
AlI3
SiI4 PI3
P2I4
+P
PI5
S2I2 ICl
ICl3
Ar
KI CaI2 ScI3 TiI2
TiI3
TiI4
VI2
VI3
CrI2
CrI3
MnI2 FeI2
FeI3
CoI2 NiI2
-Ni
CuI ZnI2 GaI
GaI3
GeI2
GeI4
+Ge
AsI3
As2I4
+As
Se IBr
IBr3
Kr
RbI
RbI3
SrI2 YI3 ZrI2
ZrI3
ZrI4
NbI4
NbI5
MoI2
MoI3
TcI3 RuI3 RhI3 PdI2 AgI CdI2 InI
InI3
SnI2
SnI4
SbI3
+Sb
TeI4
+Te
I
I
3
Xe
CsI
CsI3
BaI2   LuI3 HfI3
HfI4
TaI4
TaI5
WI2
WI3
WI4
ReI3
ReI
4
OsI
OsI2
OsI3
IrI3
IrI
4
PtI2
PtI4
AuI
AuI3
Hg2I2
HgI2
TlI
TlI3
PbI2 BiI3 PoI2
PoI4
AtI Rn
Fr RaI2   Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
LaI2
LaI3
CeI2
CeI3
PrI2
PrI3
NdI2
NdI3
PmI3 SmI2
SmI3
EuI2
EuI3
GdI2
GdI3
TbI3 DyI2
DyI
3
HoI3 ErI3 TmI2
TmI3
YbI2
YbI3
AcI3 ThI2
ThI3
ThI4
PaI4
PaI5
UI3
UI4
NpI3 PuI3 AmI2
AmI3
CmI3 BkI
3
CfI
2

CfI
3
EsI2
EsI3
Fm Md No