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Ammonium fluorosilicate

From Wikipedia, the free encyclopedia
Chemical compound
Ammonium fluorosilicate
Ball-and-stick model for a unit cell.
Two crystals with small light yellow-orange ice-like grains twining side-by-side, but a clear gap between; selenium contamination darkens the left one.
Names
IUPAC name
Ammonium hexafluorosilicate
Other names
Ammonium fluorosilicate

Ammonium fluosilicate

Ammonium silicofluoride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.037.229Edit this at Wikidata
EC Number
  • 240-968-3
RTECS number
  • VV7800000
UNII
UN number2854
  • InChI=1S/F6Si.2H3N/c1-7(2,3,4,5)6;;/h;2*1H3/q-2;;/p+2 checkY
    Key: ITHIMUMYFVCXSL-UHFFFAOYSA-P checkY
  • InChI=1/F6Si.2H3N/c1-7(2,3,4,5)6;;/h;2*1H3/q-2;;/p+2
    Key: ITHIMUMYFVCXSL-SKRXCDHZAK
  • F[Si-2](F)(F)(F)(F)F.[NH4+].[NH4+]
  • [NH4+].[NH4+].F[Si--](F)(F)(F)(F)F
Properties
(NH4)2[SiF6]
AppearanceWhite crystals
Density2.0 g cm−3
Melting point100 °C (212 °F; 373 K) (decomposes)[1]
Solubilitydissolves inwater andalcohol
Related compounds
Othercations
Hexafluorosilicic acid

Sodium fluorosilicate

Hazards[2][3]
GHS labelling:
CorrosiveAcute Toxicitytarget organ toxicity
Danger
H301,H311,H315,H319,H331,H335,H372
P260,P261,P264,P270,P271,P280,P301+P310,P302+P352,P304+P340,P305+P351+P338,P312,P314,P321,P330,P332+P313,P337+P313,P362,P403+P233,P405,P501
NFPA 704 (fire diamond)
Safety data sheet (SDS)ChemicalBook MSDS
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

Ammonium fluorosilicate (also known as ammonium hexafluorosilicate, ammonium fluosilicate or ammonium silicofluoride) has the formula (NH4)2SiF6. It is a toxic chemical, like all salts offluorosilicic acid.[4] It is made of white crystals,[5] which have at least threepolymorphs[6] and appears in nature as rare minerals cryptohalite orbararite.

Structure

[edit]

Ammonium fluorosilicate has three majorpolymorphs: α-(NH4)2[SiF6] form iscubic (space group Fm3m, No. 225) and corresponds to the mineral cryptohalite. The β form istrigonal (scalenohedral) and occurs in nature as mineral bararite.[7] A third (γ) form was discovered in 2001 and identified with thehexagonal 6mm symmetry. In all three configurations, the [SiF6]2−octahedra are arranged in layers. In the α form, these layers are perpendicular to[111] directions. In the β- and γ- forms, the layers are perpendicular to the c-axis.[6] (Note: trigonal symmetry is part of the hexagonal group, but not all hexagonal crystals are trigonal.[8]) The silicon atoms of α-(NH4)2[SiF6] (alpha), havecubic close packing (CCP). The γ form hashexagonal close packing and the β-(NH4)2[SiF6] has primitive hexagonal packing.[9] In all three phases, 12fluorine atoms neighbor the (NH4)+.[6]

Although bararite was claimed to bemetastable atroom temperature,[10] it does not appear onepolymorph has ever turned into another.[6] Still, bararite is fragile enough that grinding it forspectroscopy will produce a little cryptohalite.[11] Even so, ammonium fluorosilicate assumes a trigonal form at pressures of 0.2 to 0.3GPa. The reaction is irreversible. If it is not bararite, the phase is at least very closely related.[6]

Thehydrogen bonding in (NH4)2[SiF6] allows this salt to change phases in ways that normal salts cannot. Interactions betweencations andanions are especially important in howammonium salts change phase.[6] (To learn more about the β-structure, seeBararite.)

Natural occurrence

[edit]

This chemical makes rare appearances in nature.[12] It is found as a sublimation product offumaroles andcoal fires. As a mineral, it is either called cryptohalite orbararite, the two being two polymorphs of the compound.[7]

Chemical properties and health hazards

[edit]

Ammonium fluorosilicate is noncombustible, but it will still release dangerous fumes in a fire, includinghydrogen fluoride,silicon tetrafluoride, andnitrogen oxides. It willcorrodealuminium. In water, ammonium fluorosilicate dissolves to form an acid solution.[5]

Inhaling dust can lead to pulmonary irritation, possibly death. Ingestion may also prove fatal. Irritation of the eyes comes from contact with the dust, as well as irritation or ulceration of the skin.[5]

Uses

[edit]

Ammonium fluorosilicate finds use as a disinfectant, and it is useful in etching glass, metal casting, and electroplating.[5] It is also used to help neutralize washing machine water aslaundry sour.

See also

[edit]
Wikimedia Commons has media related toDiammonium hexafluorosilicate.

References

[edit]
  1. ^ammonium silicofluoride
  2. ^"Ammonium Hexafluorosilicate".PubChem. National Institute of Health. RetrievedOctober 12, 2017.
  3. ^"SAFETY DATA SHEET Ammonium hexafluorosilicate, 99.999%".Fisher Scientific. Archived fromthe original on 2017-10-16. RetrievedOctober 15, 2017.
  4. ^Wiberg, E., Wiberg, N., and Holleman, A. F. (2001)Inorganic chemistry. Academic Press, San Diego.
  5. ^abcdAmmonium fuorosilicate, CAMEO Chemicals, NOAA
  6. ^abcdefBoldyreva, E. V.; Shakhtshneider, T. P.; Sowa, H.; Ahsbas, H. (2007). "Effect of hydrostatic pressure up to 6 GPa on the crystal structures of ammonium and sodium hexafluorosilicates, (NH4)2[SiF6] and Na2[SiF6]; a phase transition in (NH4)2[SiF6] at 0.2–0.3 GPa".Zeitschrift für Kristallographie.222:23–29.doi:10.1524/zkri.2007.222.1.23.S2CID 97174719.
  7. ^abAnthony, J. W., Bideaux, R. A., Bladh, K. W., and Nichols, M. C. (1997)Handbook of Mineralogy, Volume III:Halides, Hydroxides, Oxides. Mineral Data Publishing, Tucson.
  8. ^Klein, C. and Dutrow, B. (2008)The 23rd Edition of the Manual of Mineral Science. John Wiley & Sons, Hoboken, NJ.
  9. ^To learn about the primitive hexagonal structure, seePrimitive hexagonal packingArchived 2009-05-26 at theWayback Machine.
  10. ^Schlemper, Elmer O. (1966). "Structure of Cubic Ammonium Fluosilicate: Neutron-Diffraction and Neutron-Inelastic-Scattering Studies".The Journal of Chemical Physics.44 (6):2499–2505.Bibcode:1966JChPh..44.2499S.doi:10.1063/1.1727071.
  11. ^Oxton, I. A., Knop, O., and Falk, M. (1975)"Infrared Spectra of the Ammonium Ion in Crystals". II. The Ammonium Ion in Trigonal Environments, with a Consideration of Hydrogen Bonding.Canadian Journal of Chemistry, 53, 3394–3400.
  12. ^Barnes, J. and Lapham, D. (1971) "Rare Minerals Found in Pennsylvania".Pennsylvania Geology, 2, 5, 6–8.

External links

[edit]


Salts and covalent derivatives of thefluoride ion
HF?HeF2
LiFBeF2BF
BF3
B2F4
+BO3
CF4
CxFy
+CO3
NF3
FN3
N2F2
NF
N2F4
NF2
?NF5
+N
+NO3
OF2
O2F2
OF
O3F2
O4F2
?OF4
F2Ne
NaFMgF2AlF
AlF3
SiF4P2F4
PF3
PF5
+PO4
S2F2
SF2
S2F4
SF3
SF4
S2F10
SF6
+SO4
ClF
ClF3
ClF5
?ArF2
?ArF4
KFCaF
CaF2
ScF3TiF2
TiF3
TiF4
VF2
VF3
VF4
VF5
CrF2
CrF3
CrF4
CrF5
?CrF6
MnF2
MnF3
MnF4
?MnF5
FeF2
FeF3
FeF4
CoF2
CoF3
CoF4
NiF2
NiF3
NiF4
CuF
CuF2
?CuF3
ZnF2GaF2
GaF3
GeF2
GeF4
AsF3
AsF5
Se2F2
SeF4
SeF6
+SeO3
BrF
BrF3
BrF5
KrF2
?KrF4
?KrF6
RbFSrF
SrF2
YF3ZrF2
ZrF3
ZrF4
NbF4
NbF5
MoF4
MoF5
MoF6
TcF4
TcF
5

TcF6
RuF3
RuF
4

RuF5
RuF6
RhF3
RhF4
RhF5
RhF6
PdF2
Pd[PdF6]
PdF4
?PdF6
Ag2F
AgF
AgF2
AgF3
CdF2InF
InF3
SnF2
SnF4
SbF3
SbF5
TeF4
?Te2F10
TeF6
+TeO3
IF
IF3
IF5
IF7
+IO3
XeF2
XeF4
XeF6
?XeF8
CsFBaF2 LuF3HfF4TaF5WF4
WF5
WF6
ReF4
ReF5
ReF6
ReF7
OsF4
OsF5
OsF6
?OsF
7

?OsF
8
IrF2
IrF3
IrF4
IrF5
IrF6
PtF2
Pt[PtF6]
PtF4
PtF5
PtF6
AuF
AuF3
Au2F10
?AuF6
AuF5•F2
Hg2F2
HgF2
?HgF4
TlF
TlF3
PbF2
PbF4
BiF3
BiF5
PoF2
PoF4
PoF6
AtF
?AtF3
?AtF5
RnF2
?RnF
4

?RnF
6
FrFRaF2 LrF3RfDbSgBhHsMtDsRgCnNhFlMcLvTsOg
LaF3CeF3
CeF4
PrF3
PrF4
NdF2
NdF3
NdF4
PmF3SmF
SmF2
SmF3
EuF2
EuF3
GdF3TbF3
TbF4
DyF2
DyF3
DyF4
HoF3ErF3TmF2
TmF3
YbF2
YbF3
AcF3ThF2
ThF3
ThF4
PaF4
PaF5
UF3
UF4
UF5
UF6
NpF3
NpF4
NpF5
NpF6
PuF3
PuF4
PuF5
PuF6
AmF2
AmF3
AmF4
?AmF6
CmF3
CmF4
 ?CmF6
BkF3
BkF
4
CfF3
CfF4
EsF3
EsF4
?EsF6
FmMdF3No
PF6,AsF6,SbF6 compounds
AlF2−5,AlF3−6 compounds
chlorides, bromides, iodides
and pseudohalogenides
SiF2−6,GeF2−6 compounds
Oxyfluorides
Organofluorides
with transition metal,
lanthanide, actinide, ammonium
nitric acids
bifluorides
thionyl, phosphoryl,
and iodosyl
Ammonium salts
Inorganic salts
monatomic anions
oxyanions
other anions
Organic salts
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