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IRON (II) OXIDE, also known as wustite, is a black cubic crystal with a density of 5.7g/cm3. It melts at 1,377°C and is insoluble in water and alkalies but dissolves in acids. When iron is heated in a low partial pressure of oxygen above 575°C, FeO is formed. However, it is only stable at high temperatures and decomposes into iron and Fe304 when cooled slowly. To obtain crystalline FeO, the high-temperature product must be quenched rapidly to stop this disproportionation. Below 198°K (the Néel temperature), FeO is antiferromagnetic and crystallizes with the rock salt structure, having four Fe2+ and four O2ions per unit cell.

1345-25-1

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1345-25-1 Usage

Uses

Used in Glass Manufacturing:
IRON (II) OXIDE is used as a dye or pigment in the manufacture of green, heat-absorbing glass for buildings and automobiles.
Used in Steel Production:
IRON (II) OXIDE is used as a precursor in the production of steel.
Used in Ceramics and Enamels:
IRON (II) OXIDE is used in ceramic mixtures and enamels.
Used in Cosmetics and Tattoo Inks:
IRON (II) OXIDE is used in cosmetics and some tattoo inks.
Used in Water Filtration:
IRON (II) OXIDE can be used for filtering phosphates from home aquaria.
Used as a Catalyst:
IRON (II) OXIDE acts as a catalyst in a number of industrial and chemical operations.
Used in the Mineral Wustite:
IRON (II) OXIDE occurs in the mineral wustite and is used in the manufacture of heat-absorbing green glasses.

Preparation

Iron(II) oxide may be prepared by thermal decomposition of iron(II) oxalate: FeC2O4 → FeO + CO + CO2 The product obtained above is impure, that may contain small quantities of triiron tetroxide, Fe3O4 and carbon. The oxide is stable above 575°C. Thus, it can be prepared by heating iron with oxygen under appropriate pressure at 575°C. Also, iron(II) oxide has been prepared by saturating the fused triiron tetroxide with iron, powdering the mixture, followed by magnetic separation of the oxide from excess iron (Sidgwick, N.V. 1950. The Chemical Elements and Their Compounds, Vol.2, pp 1328, Oxford: Clarendon Press).

Check Digit Verification of cas no

The CAS Registry Mumber 1345-25-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,3,4 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1345-25:
(6*1)+(5*3)+(4*4)+(3*5)+(2*2)+(1*5)=61
61 % 10 = 1
So 1345-25-1 is a valid CAS Registry Number.
InChI:InChI=1/Fe.O/rFeO/c1-2

1345-25-1 Well-known Company Product Price

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  • Alfa Aesar

  • (30513)  Iron(II) oxide, 99.5% (metals basis)   

  • 1345-25-1

  • 5g

  • 809.0CNY

  • Detail
  • Alfa Aesar

  • (30513)  Iron(II) oxide, 99.5% (metals basis)   

  • 1345-25-1

  • 25g

  • 4270.0CNY

  • Detail
  • Aldrich

  • (400866)  Iron(II)oxide  −10 mesh, 99.9% trace metals basis

  • 1345-25-1

  • 400866-5G

  • 892.71CNY

  • Detail
  • Aldrich

  • (400866)  Iron(II)oxide  −10 mesh, 99.9% trace metals basis

  • 1345-25-1

  • 400866-25G

  • 2,868.84CNY

  • Detail

1345-25-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ferrous oxide

1.2 Other means of identification

Product number -
Other names Natural wuestite

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1345-25-1 SDS

1345-25-1Synthetic route

iron(III) oxide

iron(III) oxide

iron(II) oxide
1345-25-1

iron(II) oxide

Conditions
ConditionsYield
With water; hydrogen In neat (no solvent) byproducts: Fe; formation of FeO at 800°C;;92%
With water; hydrogen In neat (no solvent) byproducts: Fe; formation of FeO at 700°C;;85%
With hydrogen In neat (no solvent) redn. of Fe2O3 in a stream of H2 below red heat;;
1-trimethylsilyl-μ3-S,S'-ethylenedithiolatohexacarbonyldiiron

1-trimethylsilyl-μ3-S,S'-ethylenedithiolatohexacarbonyldiiron

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

iron sulfide

iron sulfide

C

(CH3)3SiC2H3S10Fe3

(CH3)3SiC2H3S10Fe3

Conditions
ConditionsYield
In decane byproducts: Me3SiCHCH2, CH2CH2, CH3CHCH2; O2 atmosphere; decompn. (170°C, 8 h); further byproducts: (Me3Si)2O, (Me2SiO)3 and (Me2SiO)4; GLC, chromato-mass spectroscopy;A 20%
B 70%
C 10%
iron(II,III) oxide

iron(II,III) oxide

iron(II) oxide
1345-25-1

iron(II) oxide

Conditions
ConditionsYield
In neat (no solvent) formation of FeO during 24 h at 600°C;;51%
In neat (no solvent) formation of FeO during 24 h at 592°C;;24%
In neat (no solvent) preparation of FeO in the high-frequenzy induction furnace;;
iron sulfide

iron sulfide

calcium oxide

calcium oxide

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

iron calcium oxysulfide

iron calcium oxysulfide

Conditions
ConditionsYield
In neat (no solvent) pressed into pellets, fired at 1190 K for 4 h in flowing He; obtained as a mixt.;A 1%
B n/a
iron pentacarbonyl
13463-40-6

iron pentacarbonyl

hydrogen
1333-74-0

hydrogen

A

iron(II,III) oxide

iron(II,III) oxide

B

iron(II) oxide
1345-25-1

iron(II) oxide

C

iron(III) oxide

iron(III) oxide

D

cementite

cementite

E

iron
7439-89-6

iron

Conditions
ConditionsYield
In neat (no solvent, gas phase) mixt. of vapor of Fe(CO)5 and H2 decomposed by plasma-chemical decomposition on Al2O3; monitored by XRD;A n/a
B n/a
C n/a
D 1%
E n/a
iron oxide

iron oxide

iron(II) titanate

iron(II) titanate

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

Fe2.40Ti0.60O4

Fe2.40Ti0.60O4

Conditions
ConditionsYield
In neat (no solvent, solid phase) ball milled Fe2TiO4 was mixed with stoich. amts. of Fe3O4; ball milled for 10 min; placed in steel crucible; heated at 950°C for 60 h under Ar; cooled in furnace under Ar atm. to 400°C; air cooled to room temp.; identified by X-ray diffraction;A 1%
B n/a
iron pentacarbonyl
13463-40-6

iron pentacarbonyl

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

iron(III) oxide

iron(III) oxide

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 160℃; for 2h; Heating / reflux;
iron(III) phosphate
765207-04-3

iron(III) phosphate

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

phosphorus pentoxide

phosphorus pentoxide

Conditions
ConditionsYield
In neat (no solvent) the equilibrium constant was determined;;
iron(II) metasilicate

iron(II) metasilicate

iron(II) oxide
1345-25-1

iron(II) oxide

Conditions
ConditionsYield
With methyllithium In neat (no solvent) byproducts: SiO2; heating iron(II)-silicate for 1 h at 1200°C in presence of excess of lime; dissociation in FeO and SiO2;;>99
iron(III) oxide

iron(III) oxide

A

iron(II,III) oxide

iron(II,III) oxide

B

iron(II) oxide
1345-25-1

iron(II) oxide

Conditions
ConditionsYield
With carbon In neat (no solvent, solid phase) byproducts: CO, CO2; under Ar, mixt. of Fe2O3 and C heated at 800°C for 1 h; identified by X-ray analysis;
iron(III) oxide

iron(III) oxide

A

iron(II,III) oxide

iron(II,III) oxide

B

iron(II) oxide
1345-25-1

iron(II) oxide

C

iron
7439-89-6

iron

Conditions
ConditionsYield
With H2 or CO In neat (no solvent) redn. of Fe2O3 in a stream of H2 or CO; first formation of Fe3O4; at higher temp. formation of FeO and Fe;;
With H2 or CO In neat (no solvent) redn. of Fe2O3 in a stream of H2 or CO; first formation of Fe3O4; at higher temp. formation of FeO and Fe;;
iron(III) oxide

iron(III) oxide

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

iron
7439-89-6

iron

Conditions
ConditionsYield
With carbon dioxide; carbon monoxide In neat (no solvent) byproducts: C; redn. of at 400°C calcined Fe2O3 starts at 200-230°C; with begin of FeO-formation starts pptn. of carbon; pptn. of carbon ends with formation of Fe;;
In neat (no solvent) redn. of Fe2O3 in carbon to FeO and Fe below 100°C;;
iron(III) oxide

iron(III) oxide

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

oxygen
80937-33-3

oxygen

Conditions
ConditionsYield
dissocn. of Fe2O3 in glass to O2 and FeO about 1300°C;;
decompn. of Fe2O3 to FeO and oxygen;;
dissocn. of Fe2O3 in glass to O2 and FeO about 1300°C;;
decompn. of Fe2O3 to FeO and oxygen;;
boron trioxide

boron trioxide

iron(III) oxide

iron(III) oxide

iron(II) oxide
1345-25-1

iron(II) oxide

Conditions
ConditionsYield
In melt byproducts: 3B2O3*2FeO*2Fe2O3;; melting in the air for a long period of time;;
iron(III) oxide

iron(III) oxide

water
7732-18-5

water

hydrogen
1333-74-0

hydrogen

iron(II) oxide
1345-25-1

iron(II) oxide

Conditions
ConditionsYield
exactly controlled H2O/H2 ratio, sufficiently high flow rate of gas mixt., use of lowly sintered well powdered Fe2O3;
iron sulfide

iron sulfide

iron(III) oxide

iron(III) oxide

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

sulfur dioxide
7446-09-5

sulfur dioxide

Conditions
ConditionsYield
In neat (no solvent) byproducts: Fe3O4; heating of an oxide-sulfide-mixture in an N2-stream;; no formation of FeO below 900°C;;A 0%
B n/a
iron(III) oxide

iron(III) oxide

zinc sulfide

zinc sulfide

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

sulfur dioxide
7446-09-5

sulfur dioxide

C

zinc(II) oxide

zinc(II) oxide

Conditions
ConditionsYield
direct smelting of sulfide ores; unreduced Fe2O3 roasts zinc blende;;
iron(III) oxide

iron(III) oxide

iron(II) oxide
1345-25-1

iron(II) oxide

Conditions
ConditionsYield
In neat (no solvent) neutral atmosphere; 1300°C;
In melt equilibrium constant was determined;;
In neat (no solvent) complete reaction at elevated temps.;;
iron(III) oxide

iron(III) oxide

iron

iron

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

iron oxide

iron oxide

Conditions
ConditionsYield
In neat (no solvent, solid phase) powders of Fe2O3 + αFe (25 or 50%) were treated in a planetary high-energy ball mill for up to 3 h; powder XRD; Moessbauer spectra;
iron(III) oxide

iron(III) oxide

hydrogen
1333-74-0

hydrogen

iron(II) oxide
1345-25-1

iron(II) oxide

Conditions
ConditionsYield
280-300°C;
500°C;
iron(III) oxide

iron(III) oxide

copper(I) sulfide
22205-45-4

copper(I) sulfide

A

copper(I) oxide

copper(I) oxide

B

iron(II) oxide
1345-25-1

iron(II) oxide

C

iron(III) sulfate

iron(III) sulfate

D

copper(II) ferrite

copper(II) ferrite

E

copper(II) oxide

copper(II) oxide

Conditions
ConditionsYield
With air byproducts: SO2, SO3; mixing of Fe2O3 and Cu2S (1:1) mech. before roasting; information about the react. eqs. in detail, about dependence on temp. from 300 till 550°C and about the effect of Fe2O3; further products;
With air byproducts: SO2, SO3; mixing of Fe2O3 and Cu2S (1:1) mech. before roasting; information about the react. eqs. in detail, about dependence on temp. from 300 till 550°C and about the effect of Fe2O3; further products;
iron(III) oxide

iron(III) oxide

copper(I) sulfide
22205-45-4

copper(I) sulfide

A

copper(I) oxide

copper(I) oxide

B

iron(II) oxide
1345-25-1

iron(II) oxide

C

copper(II) ferrite

copper(II) ferrite

D

copper(II) oxide

copper(II) oxide

Conditions
ConditionsYield
byproducts: SO2, SO3; at roasting of Cu2S in presence of Fe2O3;
indium(III) oxide

indium(III) oxide

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

indium
7440-74-6

indium

Conditions
ConditionsYield
In neat (no solvent) (Ar); In2O3 and Fe reacted in 1:1 or 1:2 or 2:1 molar ratio; powdered inmortar; sealed under vacuum in quartz ampoule; heated to 723 K and with 0.5 K/h to 973 K; maintained for 7 days; cooled to 0.8 K/h to 473 K; le ft standing at room temp.;
iron sulfide

iron sulfide

water
7732-18-5

water

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

hydrogen sulfide
7783-06-4

hydrogen sulfide

water
7732-18-5

water

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

iron(III) oxide

iron(III) oxide

Conditions
ConditionsYield
In neat (no solvent) byproducts: H2; thin layer of FeO (71.5%) and Fe2O3 (26.34%) is formed inside a steam pipe; better reaction in the presence of O2 or CO2, formation of some H2;;
In neat (no solvent) byproducts: H2; thin layer of FeO (71.5%) and Fe2O3 (26.34%) is formed inside a steam pipe; better reaction in the presence of O2 or CO2, formation of some H2;;
water
7732-18-5

water

A

iron(II,III) oxide

iron(II,III) oxide

B

iron(II) oxide
1345-25-1

iron(II) oxide

C

iron(III) oxide

iron(III) oxide

Conditions
ConditionsYield
In neat (no solvent) react. of Fe with water vapor at 700°C; cooling on air;; radiographic anal.;;
water
7732-18-5

water

iron(II) oxide
1345-25-1

iron(II) oxide

Conditions
ConditionsYield
With oxygen In neat (no solvent) byproducts: Fe2O3, Fe3O4; iron foil was treated with a steam/N2 mixt. with added air (0.13-1.44% O2) at 800°C for 1 h; product samples (thin films) were investigated by gravimetric anal., Auger and X-ray spectroscopy, scanning electron microscopy;
In neat (no solvent) byproducts: Fe3O4; iron foil was treated with steam/N2 mixts. at 540-800°C for 3-17h; growth rate and composition of the product depend on the foil thickness, H2O flow rate, reaction time and temp.; product samples (thin films) were investigated by gravimetric anal., Auger and X-ray spectroscopy, scanning electron microscopy;
In neat (no solvent) byproducts: H2; oxidation of Fe with water vapor above 500°C;;
water
7732-18-5

water

A

iron(II) oxide
1345-25-1

iron(II) oxide

B

hydrogen
1333-74-0

hydrogen

Conditions
ConditionsYield
In water reaction of iron shavings with water at 100°C in air or N2 atmosphere;;
H2O/H2 equil. ratio detd.;
study of chemical equil.;
pyrite

pyrite

water
7732-18-5

water

iron(II) oxide
1345-25-1

iron(II) oxide

Conditions
ConditionsYield
In neat (no solvent) heating pyrite in water vapor at 300-400°C;;
carbon disulfide
75-15-0

carbon disulfide

iron(II) oxide
1345-25-1

iron(II) oxide

dimethyl amine
124-40-3

dimethyl amine

ferric dimethyldithiocarbamate

ferric dimethyldithiocarbamate

Conditions
ConditionsYield
With zinc(II) oxide In water at 20℃; for 8h; Reflux; Large scale;99%
iron(II) oxide
1345-25-1

iron(II) oxide

strontium hydrogenphosphate

strontium hydrogenphosphate

phosphoric acid
86119-84-8, 7664-38-2

phosphoric acid

SrFe3(9+)*3PO4(3-)=SrFe3(PO4)3

SrFe3(9+)*3PO4(3-)=SrFe3(PO4)3

Conditions
ConditionsYield
In water hydrothermal method; heating (sealed quartz tube, 648 K, 3 d), cooling (2 h to room temp.); filtration, washing (water, acetone), drying (335 K, 1 h); elem anal. (EDX), detn. by powder XRD;91%
iron(II) oxide
1345-25-1

iron(II) oxide

iron(III) oxide

iron(III) oxide

ammonium dihydrogen phosphate
7722-76-1

ammonium dihydrogen phosphate

ammonium iron(II,III) phosphate

ammonium iron(II,III) phosphate

Conditions
ConditionsYield
In water sealed gold ampoule, 500°C (32000 psi autogenous pressure), 24 h;cooling to 250°C at 3°C/h, quenching to room temp.;85%
iron(II) oxide
1345-25-1

iron(II) oxide

iron(III) phosphate
765207-04-3

iron(III) phosphate

(x)H2O*(x)H3O4P

(x)H2O*(x)H3O4P

calcium hydroxide

calcium hydroxide

Ca(2+)*4Fe(3+)*Fe(2+)*5PO4(3-)*OH(1-)*H2O=CaFe5(PO4)5(OH)*H2O

Ca(2+)*4Fe(3+)*Fe(2+)*5PO4(3-)*OH(1-)*H2O=CaFe5(PO4)5(OH)*H2O

Conditions
ConditionsYield
In further solvent(s) High Pressure; heating in autoclave, 400°C, 2.5 d; cooling to room temp. within 8h; detn. by X-ray powder diffraction;84%
iron(II) oxide
1345-25-1

iron(II) oxide

2,2,6,6-tetramethylheptane-3,5-dione
1118-71-4

2,2,6,6-tetramethylheptane-3,5-dione

iron(III) 2,2,6,6-tetramethyl-3,5-heptadionate

iron(III) 2,2,6,6-tetramethyl-3,5-heptadionate

Conditions
ConditionsYield
With O2 In further solvent(s) dione as solvent, reflux for 24 h under O2; cooling to room temp., evapn. in vac., extn. with acetone, evapn. at room temp. in air or in vac., sublimation, recrystn. from EtOH, elem. anal.;60%
iron(II) oxide
1345-25-1

iron(II) oxide

C22H20N5(1+)*Cl(1-)

C22H20N5(1+)*Cl(1-)

C44H36FeN10(2+)*2Cl(1-)

C44H36FeN10(2+)*2Cl(1-)

Conditions
ConditionsYield
In dimethyl sulfoxide at 110℃; under 7500.75 Torr; for 24h; Inert atmosphere;38%
iron(II) oxide
1345-25-1

iron(II) oxide

phosphorus pentoxide
16752-60-6

phosphorus pentoxide

rubidium chloride

rubidium chloride

sodium chloride
7647-14-5

sodium chloride

Rb(1+)*3Na(1+)*7Fe(2+)*6PO4(3-) = RbNa3Fe7(PO4)6

Rb(1+)*3Na(1+)*7Fe(2+)*6PO4(3-) = RbNa3Fe7(PO4)6

Conditions
ConditionsYield
In melt byproducts: (RbCl)Na2Fe3(P2O7)2, NaFe3.67(PO4)3; FeO and P4O10 ground in RbCl/NaCl flux and placed in carbon-coated fused-silica ampoule; sealed under vac.; heated to 700°C and held at this temp. for 4 d; slowly cooled to 450°C and finally cooled to room temp.;20%
iron(II) oxide
1345-25-1

iron(II) oxide

sodium glycinate
6000-44-8

sodium glycinate

ferrous glycinate
20150-34-9

ferrous glycinate

Conditions
ConditionsYield
With citric acid In water at 55 - 60℃; for 1h;
iron(II) oxide
1345-25-1

iron(II) oxide

strontium(II) carbonate
1633-05-2

strontium(II) carbonate

bismuth(III) oxide
1304-76-3

bismuth(III) oxide

Bi10Sr15Fe10O46

Bi10Sr15Fe10O46

Conditions
ConditionsYield
In neat (no solvent) alumina crucible, heating (1250°C), cooling (800°C, 105 h), annealing (765°C, 0.2% O2 or 60 atm O2), slow cooling (from 500to 350°C), holding (350 degree.C, 2 wk);
iron(II) oxide
1345-25-1

iron(II) oxide

iron(III) oxide

iron(III) oxide

indium(III) oxide

indium(III) oxide

zinc(II) oxide

zinc(II) oxide

InFeO3(ZnO)(FeO)

InFeO3(ZnO)(FeO)

Conditions
ConditionsYield
heating (sealed Pt tube, 1200°C, 1 d), rapid cooling in air;
iron(II) oxide
1345-25-1

iron(II) oxide

iron(III) oxide

iron(III) oxide

barium cyanide

barium cyanide

A

Prussian blue
14038-43-8

Prussian blue

B

barium(II) oxide

barium(II) oxide

Conditions
ConditionsYield
glowing;
iron(II) oxide
1345-25-1

iron(II) oxide

iron(III) oxide

iron(III) oxide

Conditions
ConditionsYield
In neat (no solvent) Electrolysis; warming mixture of FeO and Fe2O3 with direct current (needed for electrolysis) in chamotte tube, pptn. of Fe occurs at 1700°C on cathode, current efficiency depends on temperature, but is very low in common;;
In melt Electrolysis; electrolyzing melt of FeO, Fe2O3 and SiO2 at 1300°C with high current density and terminal voltage 1.7 to 2 V leads to pptn. of iron sponge;;

1345-25-1Related news

Influence of iron (II) oxide nanoparticle on biohydrogen production in thermophilic mixed fermentation09/02/2019

The effect of initial pH, metal oxide and concentration of nanoparticles (NP) on hydrogen production were investigated in batch assays using glucose-fed anaerobic mixed bacteria in thermophilic condition of 60 °C. Two type of metal oxide nanoparticles, iron (II) oxide and nickel oxide, were tes...detailed

1345-25-1Relevant academic research and scientific papers

Reduction of FeO/Pt(1 1 1) thin films by exposure to atomic hydrogen

Knudsen, Jan,Merte, Lindsay R.,Grabow, Lars C.,Eichhorn, Falk M.,Porsgaard, Soeren,Zeuthen, Helene,Vang, Ronnie T.,L?gsgaard, Erik,Mavrikakis, Manos,Besenbacher, Flemming

, p. 11 - 20 (2010)

Using scanning tunneling microscopy (STM), X-ray photoemission spectroscopy (XPS) and density functional theory (DFT) calculations we have studied the reduction of ultra-thin films of FeO(1 1 1) grown on Pt(1 1 1) after exposure to atomic hydrogen at room temperature. A number of new ordered, partly-reduced FeOx structures are identified and as a general trend we reveal that all the reduced FeOx structures incorporate 2-fold coordinated Fe atoms as opposed to the original 3-fold coordinated Fe atoms in the FeO film. We find that when all the Fe atoms are 2-fold O-coordinated the FeOx surface structure is resistant to further reduction at room temperature. We observe that water easily dissociates on the most heavily reduced FeOx, structure in contrast to the initially inert FeO film, and reveal that it is possible to partially re-oxidize the FeOx film by heating the surface slightly in the presence of water.

Studies on structural, magnetic and thermal properties of xFe 2TiO4-(1-x)Fe3O4 (0≤x≤1) pseudo-binary system

Sorescu, Monica,Xu, Tianhong,Wise, Adam,Díaz-Michelena, Marina,McHenry, Michael E.

, p. 1453 - 1462 (2012)

The xFe2TiO4-(1-x)Fe3O4 pseudo-binary systems (0≤x≤1) of ulv?spinel component were synthesized by solid-state reaction between ulv?spinel Fe 2TiO4 precursors and commercial Fe3O

Radiative lifetimes of the FeO orange system

Son,Lee,Shin,Ku

, p. 658 - 664 (2000)

The ground-state FeO molecules are generated from photolysis of Fe(CO)5 in a Fe(CO)5/M(O2 or N2O)/Rg(He or Ar) mixture using an unfocused weak UV laser beam. The formation of ground-state FeO molecules is identified by a laser-induced fluorescence (LIF) method. The LIF signal from FeO molecules is stronger in O2 than in N2O at the same partial pressures. The radiative lifetimes for seven bands in the FeO orange system are measured. They are substantially different depending on the excited band ranging from 260±30 ns to 590±50 ns.

REACTION PROCESS BETWEEN alpha -IRON(III) OXIDE AND SULFUR DIOXIDE IN THE PRESENCE OF CARBON.

Araki,Ryoo,Eguchi,Matsuzaki,Saeki

, p. 2271 - 2274 (1980)

The reaction products obtained by heating a mixture of alpha -Fe//2O//3 and carbon in a SO//2 stream at various temperatures were examined. The possible reactions during the above process were also examined The solid products obtained by heating a mixture of alpha -Fe//2O//3 and carbon in a SO//2 stream were Fe//3O//4 at 500 - 700 degree C, pyrrhotite and Fe//3O//4 at 750 degree C, and pyrrhotite (Fe//0//. //8//8S) alone at 800 degree C. Sulfur was obtained outside the heating zone throughout the temperature range. The reaction between carbon and SO//2 occurs even at 350 degree C to form sulfur, and the reaction proceeds markedly above ca. 700 degree C. Above ca. 500 degree C, the reductions of alpha -Fe//2O//3 with carbon and sulfur occur to form Fe//3O//4. Above ca. 750 degree C, pyrrhotite is formed by the reaction between Fe//3O//4 and sulfur. These results were supported by the thermodynamical consideration based on the chemical potential diagram for the Fe-S-C-O system.

Hard magnetic nanocrystalline alloys of Fe-Fe2O3 system

Lileev,Yagodkin,Grishina,Khanenya,Nefedov,Popova

, p. 1217 - 1220 (2005)

The structure and magnetic properties of Fe2O3 and Fe powders as well as their mixtures, subjected to treatment in a high-energy ball mill, were studied. It was shown that the phase composition of all the starting materials (except that of the Fe powder) was changed in the milling process. The nanocrystalline composite alloys, containing FeO and α-Fe with an average crystallite size of 10-20 nm as well as an amorphous phase, were obtained as a result of the milling. Phase content in the milled powders depended on the composition of the starting materials. Unlike the starting materials, the milled powders (except of the milled Fe powder and Fe 2O3+90% Fe mixture) had the properties, which are characteristic for hard magnetic materials. Further improvement of the properties was achieved by low-temperature annealing of the milled powders. The annealed powders of the mixtures contained only nanocrystallites of α-Fe and Fe3O4. The amount of these constituents and the magnetic properties of the annealed powders depended on the composition of the starting materials. The sufficiently high properties of the produced powders may be explained by the formation of α-Fe and Fe3O4 single-domain particles.

Monolayer iron oxide film on platinum promotes low temperature CO oxidation

Sun,Qin,Lewandowski,Carrasco,Sterrer,Shaikhutdinov,Freund

, p. 359 - 368 (2009)

CO oxidation on a clean Pt(1 1 1) single crystal and thin iron oxide films grown on Pt(1 1 1) was studied at different CO:O2 ratios (between 1:5 and 5:1) and partial pressures up to 60 mbar at 400-450 K. Structural characterization of the model

Cyclic reduction-oxidation of haematite powders

Coombs, P. G.,Munir, Z. A.

, (1989)

The cyclic reduction-oxidation of haematite (Fe2O3) powders was investigated over the temperature range 723 to 873 K. The hydrogeon reduction had an approximate activation energy of 53 KJ mol-1. The air oxidation of the re

M?ssbauer and X-ray diffraction investigation of nanocrystalline Fe-O alloys

Lileev,Yagodkin,Reissner,Steiner

, p. 504 - 506 (2003)

X-ray and M?ssbauer investigations were carried out on powders produced by milling of Fe2O3 + α-Fe mixtures in a high-energy ball mill and subsequent low-temperature annealing. The nanocrystalline composite alloys obtained as a result of the milling, contained FeO and α-Fe with an average crystallite size of 15-20nm as well as an amorphous phase. Alloys subjected to subsequent annealing contained, however, only α-Fe + Fe3O4 with an average crystallite size of about 20nm. Unlike the starting materials the produced powders had properties, which are characteristic for hard magnetic materials.

Structural, magnetic and electrical properties of CoSi ferrites synthesized by sol-gel self-propagating method

Tao, Zheng-Xiong,Li, Le-Zhong,Wu, Xiao-Hui,Zhong, Xiao-Xi,Zhong, Zi-Chen

, (2021)

CoFe2O4 is mainly used in magnetic strain sensor, magnetic resonance imaging, supercapacitor, cryogen, high density magnetic recording medium and magneto-optical devices and so on. In this study, SixCo1-xFe

One-dimensional pyrazine bridged M(II)-saccharinato coordination polymers: Synthesis, characterization, crystal structures and thermal studies

Yilmaz, Veysel T.,Senel, Evrim,Kazak, Canan

, p. 3199 - 3204 (2007)

Three new coordination polymers with a general formula [M(sac)2(μ-pyz)(H2O)2]n [M = Mn(II) (1), Fe(II) (2), Co(II) (3), pyz = pyrazine, and sac = saccharinate] have been synthesized and characterized by elemental analyses, IR, UV-VIS, magnetic measurements, thermal analysis techniques and single crystal X-ray diffraction. All three complexes are isomorphous, crystallizing in the triclinic space group P over(1, ?) (No. 2). Each metal(II) ion in 1-3 is octahedrally coordinated by two sac, two pyz and two aqua ligands. The sac ligands are N-coordinated, while the pyz ligands bridge the metal centers leading to an one-dimensional linear chain structure. Intra-chain M-M separations in complexes 1, 2 and 3 are 7.381(2), 7.259(3) and 7.188(3) A?, respectively. The individual chains are linked into two-dimensional layers by O-H?O hydrogen bonds involving the hydrogens of aqua ligands and carbonyl and sulfonyl O atoms of sac ligands. The hydrogen bonded layers are further assembled into three-dimensional supramolecular networks by weak aromatic π?π stacking interactions between the phenyl rings of sac ligands or CH?π interactions involving pyz. These complexes exhibit similar decomposition characteristics. In the first stages, endothermic removal of the aqua and pyz ligand takes place leading to an intermediate probably in the form of [M(sac)2], which undergoes highly exothermic decomposition at higher temperatures to give corresponding metal oxides.

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