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Lead titanate

From Wikipedia, the free encyclopedia
Lead titanate
Tetragonal unit cell of lead titanate
Names
Other names
Lead(II) titanate
Lead titanium oxide
Lead(II) titanium oxide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.031.841Edit this at Wikidata
EC Number
  • 235-038-9
  • InChI=1S/3O.Pb.Ti/q;2*-1;+2;
    Key: NKZSPGSOXYXWQA-UHFFFAOYSA-N
  • [O-][Ti](=O)[O-].[Pb+2]
Properties
PbTiO3
Molar mass303.09 g/mol
AppearanceYellow powder
Density7.52 g/cm3
Insoluble
Hazards
GHS labelling:
GHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard[1]
Danger[1]
H302,H332,H360,H373,H410[1]
P201,P261,P273,P304+P340,P308+P313,P312,P391[1]
NFPA 704 (fire diamond)
Lethal dose or concentration (LD, LC):
12000 mg/kg (rat)
Safety data sheet (SDS)MSDS
Related compounds
Otheranions
Lead dioxide
Lead acetate
Othercations
Caesium titanate
Iron(II) titanate
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound

Lead(II) titanate is aninorganic compound with thechemical formula PbTiO3. It is theleadsalt oftitanic acid. Lead(II) titanate is a yellow powder that isinsoluble inwater.

At high temperatures, lead titanate adopts a cubicperovskite structure. At 760 K,[2] the material undergoes a second orderphase transition to a tetragonal perovskite structure which exhibits ferroelectricity. Lead titanate is one of the end members of thelead zirconate titanate (Pb[ZrxT1−x]O3,0 ≤x ≤ 1, PZT) system, which is technologically one of the most important ferroelectric andpiezoelectric ceramics;PbTiO3 has a high ratio of k33 to kp with a high kt[clarify].

Lead titanate occurs in nature as mineralmacedonite.[3][4]

Toxicity

[edit]

Lead titanate is toxic, like other lead compounds. Itirritatesskin,mucous membranes andeyes. It may also cause harm to unborn babies and might have effects on fertility.[5]

Solubility in water

[edit]

The solubility of hydrothermally-synthesized perovskite-phase PbTiO3 in water was experimentally determined at 25 and 80 °C to depend on pH and vary from 4.9x10−4 mol/kg at pH≈3, to 1.9x10−4 mol/kg at pH≈7.7, to "undetectable" (<3.2x10−7 mol/kg) in the range 10<pH<11. At still higher pH values, the solubility increased again. The solubility was apparentlyincongruent and was quantified as the analytical concentration of Pb.[6]

References

[edit]
  1. ^abcdSigma-Aldrich Co.,Lead(II) titanate. Retrieved on 2019-01-15.
  2. ^Noheda, Beatriz; Cereceda, Noé; Iglesias, Tomás; Lifante, Ginés; Gonzalo, Julio A.; Chen, Hui Ting; Wang, Yong Ling (1995-06-01)."Composition dependence of the ferroelectric-paraelectric transition in the mixed system PbZr1−xTixO3"(PDF).Physical Review B.51 (22). American Physical Society (APS):16388–16391.Bibcode:1995PhRvB..5116388N.doi:10.1103/physrevb.51.16388.ISSN 0163-1829.PMID 9978623.
  3. ^Radusinović, Dušan and Markov, Cvetko "Macedonite - lead titanate: a new mineral",American Mineralogist56, 387-394 (1971),http://www.minsocam.org/ammin/AM56/AM56_387.pdf
  4. ^Burke, E.A.J. and Kieft, C. "Second occurrence of makedonite, PbTiO3, Långban, Sweden",Lithos4, 101-104 (1971)
  5. ^"Archived copy"(PDF). Archived fromthe original(PDF) on 2011-07-19. Retrieved2010-09-12.{{cite web}}: CS1 maint: archived copy as title (link)
  6. ^Jooho Moon, Melanie L. Carasso, Henrik G. Krarup, Jeffrey A. Kerchner, "Particle-shape control and formation mechanisms of hydrothermally derived lead titanate", Journal of Materials Research, Vol. 14, No.3, March 1999.[1]
Pb(II)
Pb(II,IV)
Pb(IV)
Titanium(II)
Organotitanium(II) compounds
Titanium(III)
Organotitanium(III) compounds
Titanium(IV)
Titanate compounds
Organotitanium(IV) compounds
Titanate salts
HHe
Li2TiO3
Li4Ti5O12
BeBCNOFNe
Na2TiO3MgAlSiPSClAr
KCaTiO3ScTiVCrMnTiO3FeCoNiTiO3CuZnTiO3
Zn2TiO4
Zn2Ti3O8
GaGeAsSeBrKr
RbSrTiO3YZrNbMoTcRuRhPdAgCdInSnSbTeIXe
Cs2TiO3BaTiO3
Ba2TiO4
*LuHfTaWReOsIrPtAuHgTlPbTiO3Bi12TiO20
Bi4Ti3O12
Bi2Ti2O7
PoAtRn
FrRa**LrRfDbSgBhHsMtDsRgCnNhFlMcLvTsOg
 
*LaCePrNdPmSmEuTiO3GdTbDy2Ti2O7Ho2Ti2O7ErTmYb
**AcThPaUNpPuAmCmBkCfEsFmMdNo
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