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12031-80-0

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12031-80-0 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 12031-80-0 differently. You can refer to the following data:
1. Lithium peroxide is a white crystalline solid or pale yellow powder which is thermodynamically stable at room temperature. The substance decomposes on heating to 195°C (the exact decomposition temperature is subject to dispute) with the formation of lithium oxide and oxygen. The decomposition forms the basis for one preparation of lithium oxide. High-purity lithium peroxide may be stored for long periods of time with no significant decomposition. The reaction of carbon dioxide and lithium peroxide is noted above. When lithium peroxide is exposed to the air, lithium carbonate is the final product. Dissolving pure lithium peroxide in water produces an alkaline solution containing lithium ions and hydroperoxide ions. The decomposition of the solution is typical in that oxygen is released on heating or in the presence of a catalyst. The water solubility of lithium peroxide decreases with increasing temperature.
2. Lithium peroxide, Li2O2, Mr 45.9, 2.36 g/cm3, has an active oxygen content of 34.8%, which is the highest of all metal peroxides. Lithium peroxide is pale yellow solid, stable at ambient temperature, and not hygroscopic. On heating to about 300 °C, it loses oxygen and forms lithium monoxide.

Uses

Different sources of media describe the Uses of 12031-80-0 differently. You can refer to the following data:
1. Lithium peroxide is used in air purifiers. It is also used to produce high-purity oxygen. It acts as a catalyst for polymerization of styrene to polystyrene. Further, it serves as a curing agent for special polymers and a source of oxygen in sealed spaces such as submarines and in breathing apparatus.
2. At this time no important industrial uses of lithium peroxide are known. One interesting potential application is in the field of atmosphere regeneration for undersea and space applications, since the compound reacts with carbon dioxide to release oxygen: Li2O2+C02 -> Li2CO3 + 0.5O2.

Preparation

Lithium peroxide is prepared industrially by the reaction of lithium hydroxide monohydrate with hydrogen peroxide which yields lithium hydroperoxide monohydrate. LiOH·H20 + H202 → LiOOH·H20+H20 The hydroperoxide may be dehydrated by heating in a vacuum to yield the peroxide. 2LiOOH·H20 → Li202+H202 + 2H20

General Description

A white powder or sandy yellow granular solid. Irritates skin, eyes and mucous membranes. Used to produce a supply of high-purity oxygen.

Air & Water Reactions

Contact with water or moist air generates a large amount of heat and corrosive, alkaline lithium hydroxide [AAR 1991].

Reactivity Profile

Lithium peroxide is strongly basic and an extremely powerful oxidizing agent. Accelerates the combustion of other materials, especially organic materials, involved in a fire. Can ignite wood, paper, oil, clothing, etc. on contact. May react explosively with hydrocarbons (fuels). Exposure to heat in a closed container may result in a vigorous reaction that violently ruptures the container.

Health Hazard

TOXIC; inhalation, ingestion or contact (skin, eyes) with vapors, dusts or substance may cause severe injury, burns or death. Fire may produce irritating and/or toxic gases. Toxic fumes or dust may accumulate in confined areas (basement, tanks, hopper/tank cars, etc.). Runoff from fire control or dilution water may cause pollution.

Fire Hazard

May explode from friction, heat or contamination. These substances will accelerate burning when involved in a fire. May ignite combustibles (wood, paper, oil, clothing, etc.). Some will react explosively with hydrocarbons (fuels). Containers may explode when heated. Runoff may create fire or explosion hazard.

Flammability and Explosibility

Notclassified

Safety Profile

A powerful oxidizer and irritant to skin, eyes, and mucous membranes. A very dangerous fire hazard because it is an extremely powerful oxidizing agent. Will react with water or steam to produce heat; on contact with reducing materials, can react vigorously. See also LITHIUM COMPOUNDS, PEROXIDES, and PEROXIDES, INORGANIC.

Check Digit Verification of cas no

The CAS Registry Mumber 12031-80-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,2,0,3 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 12031-80:
(7*1)+(6*2)+(5*0)+(4*3)+(3*1)+(2*8)+(1*0)=50
50 % 10 = 0
So 12031-80-0 is a valid CAS Registry Number.
InChI:InChI=1/2Li.2O/rLi2O2/c1-3-2-4-1

12031-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Lithium peroxide

1.2 Other means of identification

Product number -
Other names Lithium Peroxide Min

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:12031-80-0 SDS

12031-80-0Synthetic route

oxygen
80937-33-3

oxygen

bis(trifluoromethane)sulfonimide lithium
90076-65-6

bis(trifluoromethane)sulfonimide lithium

lithium peroxide
12031-80-0

lithium peroxide

Conditions
ConditionsYield
With 1-butyl-methylpyrrolidinium bis(trifluoromethylsulfonyl)amide Electrochemical reaction;
lithium perchlorate

lithium perchlorate

tetramethylammonium superoxide
62205-77-0

tetramethylammonium superoxide

lithium peroxide
12031-80-0

lithium peroxide

Conditions
ConditionsYield
In acetonitrile at 20℃; for 1h; Glovebox; Inert atmosphere;
oxygen
80937-33-3

oxygen

lithium perchlorate

lithium perchlorate

lithium peroxide
12031-80-0

lithium peroxide

Conditions
ConditionsYield
With ruthenium oxide nanoparticle decorated mesoporous boron doped carbon nitride electrode In dimethyl sulfoxide at 80℃; for 48h; Mitsunobu Displacement; Electrochemical reaction; Glovebox;
lithium hydroxide monohydrate
1310-66-3

lithium hydroxide monohydrate

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

lithium peroxide
12031-80-0

lithium peroxide

Conditions
ConditionsYield
for 1h;
hydrogenchloride
7647-01-0

hydrogenchloride

lithium peroxide
12031-80-0

lithium peroxide

lithium chloride

lithium chloride

lithium hydroxide
1310-65-2

lithium hydroxide

ruthenium
7440-18-8

ruthenium

Li8Ru2OCl14

Li8Ru2OCl14

Conditions
ConditionsYield
Stage #1: lithium peroxide; lithium hydroxide; ruthenium In melt at 600℃; for 0.5h;
Stage #2: hydrogenchloride; lithium chloride
60%
lithium peroxide
12031-80-0

lithium peroxide

neptunium(IV) dioxide

neptunium(IV) dioxide

NpO6(5-)*5Li(1+)=Li5NpO6

NpO6(5-)*5Li(1+)=Li5NpO6

Conditions
ConditionsYield
In solid NpO2 and Li2O2 ground together, heated at 400°C for 24-72 h under O2; cooled, analyzed, reground, reheated until const. Np(VII) content (about 80-85%), not pure material(!);
lithium peroxide
12031-80-0

lithium peroxide

cesium oxo terbate (IV)

cesium oxo terbate (IV)

A

cesium oxide

cesium oxide

B

Cs2Li14{Tb3O14}

Cs2Li14{Tb3O14}

C

octalithium oxo terbate (IV)

octalithium oxo terbate (IV)

Conditions
ConditionsYield
In neat (no solvent) byproducts: O2; tempering (ratio Tb:Li 1:5, 550°C, closed Au-tube, 3 weeks, heating rate 10°C/h);
lithium peroxide
12031-80-0

lithium peroxide

terbium oxide

terbium oxide

cesium oxo terbate (IV)

cesium oxo terbate (IV)

Cs2Li14{Tb3O14}

Cs2Li14{Tb3O14}

Conditions
ConditionsYield
In neat (no solvent) byproducts: O2; tempering (560°C, closed Au-tube, 10 d or 8 weeks);
lithium peroxide
12031-80-0

lithium peroxide

copper(II) oxide

copper(II) oxide

lithium cuprate
12527-46-7

lithium cuprate

Conditions
ConditionsYield
With oxygen heating (platinum crucible, oxygen flow, 500°C, 5 d);
450°C for 5 d;
nickel(II) oxide
1313-99-1

nickel(II) oxide

lithium peroxide
12031-80-0

lithium peroxide

lithium nickelate(III)

lithium nickelate(III)

Conditions
ConditionsYield
educts were ground together in an argon grove box and were pelletized, pellets were heated to 850°C very slowly under a stream of pure dried O2 passed through liquid N2 (24-48 h); cooling to room temp. very slowly;
lithium peroxide
12031-80-0

lithium peroxide

oxygen
7782-44-7

oxygen

Conditions
ConditionsYield
With hydrogenchloride In neat (no solvent) solid peroxide exposured to gaseous haloid acid; not isolated, detected by emission spectroscopy;
lithium peroxide
12031-80-0

lithium peroxide

octalithium oxo terbate (IV)

octalithium oxo terbate (IV)

Conditions
ConditionsYield
With TbO(x) In neat (no solvent) in a sealed Ag-bomb, 700°C for 7 d, excess of Li2O2;;
lithium peroxide
12031-80-0

lithium peroxide

octalithium oxo praseodymate (IV)

octalithium oxo praseodymate (IV)

Conditions
ConditionsYield
With PrO(x) In neat (no solvent) sealed Ag-bomb, 700°C for 7 d, excess of Li2O2;;
cobalt(II,III) oxide

cobalt(II,III) oxide

lithium peroxide
12031-80-0

lithium peroxide

lithium cobalt(III) oxide

lithium cobalt(III) oxide

Conditions
ConditionsYield
In neat (no solvent) mixt. of Li2O2 and Co3O4 ball milled for 30 min and heated at 800°C for 5 h under air flow; detn. by induced coupled plasma (ICP) anal. and XRD;
Stage #1: cobalt(II,III) oxide; lithium peroxide With oxygen at 750℃; for 16h; Glovebox;
Stage #2: With oxygen at 700℃; for 16h;
lithium peroxide
12031-80-0

lithium peroxide

curium oxide

curium oxide

Cm(x)Li(x)O(x)

Cm(x)Li(x)O(x)

Conditions
ConditionsYield
Grounding the oxides in an agate mortar, heating the mixt. (ratio Li:Cm=8:1) for 10 min at 600°C.;
lithium peroxide
12031-80-0

lithium peroxide

lithium arsenite

lithium arsenite

lithium arsenate

lithium arsenate

Conditions
ConditionsYield
With dihydrogen peroxide In water soln. of LiAsO2 in distd. H2O, continually stirred (10 min), addn. of Li2O2, exothermic reaction, kept 20 min, addn. of 30% H2O2; filtration, evapn. (on a water bath), crystn., crystals dried in a drying cupboard at 160-170°C to constant mass (5 h); elem. anal.;99.3-99.8
lithium peroxide
12031-80-0

lithium peroxide

tellurium oxide
13451-18-8

tellurium oxide

lithium oxide

lithium oxide

Li6TeO6

Li6TeO6

Conditions
ConditionsYield
In neat (no solvent) heating (700-800°C, closed Au- or Ag-tubes);
lithium peroxide
12031-80-0

lithium peroxide

manganese(II) oxide

manganese(II) oxide

A

lithium manganate

lithium manganate

B

LiMnO3

LiMnO3

lithium peroxide
12031-80-0

lithium peroxide

manganese(II) oxide

manganese(II) oxide

Li0.33Mn0.67O

Li0.33Mn0.67O

Conditions
ConditionsYield
at 600°C;
lithium peroxide
12031-80-0

lithium peroxide

manganese(II) oxide

manganese(II) oxide

A

Li0.35Mn0.65O

Li0.35Mn0.65O

B

Li0.6Mn0.4O

Li0.6Mn0.4O

C

Li0257Mn0743O

Li0257Mn0743O

Conditions
ConditionsYield
at 900°C, tempering at 750°C;
lithium peroxide
12031-80-0

lithium peroxide

manganese(II) oxide

manganese(II) oxide

lithium manganate

lithium manganate

Conditions
ConditionsYield
in vac. for 5 h;
lithium peroxide
12031-80-0

lithium peroxide

manganese(II) oxide

manganese(II) oxide

Li0135Mn0865O

Li0135Mn0865O

Conditions
ConditionsYield
at 700°C;
lithium peroxide
12031-80-0

lithium peroxide

manganese(II) oxide

manganese(II) oxide

Li0046Mn0954O

Li0046Mn0954O

Conditions
ConditionsYield
at 600°C;
lithium peroxide
12031-80-0

lithium peroxide

manganese(II) oxide

manganese(II) oxide

(x)LiMn2O4*(y)α-Mn2O3

(x)LiMn2O4*(y)α-Mn2O3

Conditions
ConditionsYield
sintering for 24 h in a Pt vessel at 600 - 900°C under 0.3 atm Ar;
lithium peroxide
12031-80-0

lithium peroxide

manganese(II) oxide

manganese(II) oxide

Li0308Mn0692O

Li0308Mn0692O

Conditions
ConditionsYield
at 800°C;
lithium peroxide
12031-80-0

lithium peroxide

uranium oxide

uranium oxide

Li6O6U, α

Li6O6U, α

Conditions
ConditionsYield
heating at 600°C for 7 days;;
heating at 910°C for 3 days; at 800°C for 5 days; at 660°C for 7 days; cooling;;
nickel(II) oxide
1313-99-1

nickel(II) oxide

lithium peroxide
12031-80-0

lithium peroxide

Li0.96Ni1.04O2

Li0.96Ni1.04O2

Conditions
ConditionsYield
In neat (no solvent) (Ar), mixing, pelletizing, heating (flowing O2, 850°C, 48 h);
nickel(II) oxide
1313-99-1

nickel(II) oxide

lithium peroxide
12031-80-0

lithium peroxide

Li0.92Ni1.08O2

Li0.92Ni1.08O2

Conditions
ConditionsYield
In neat (no solvent) (Ar), mixing, pelletizing, heating (flowing O2, 900°C, 48 h);
sodium oxide

sodium oxide

lithium peroxide
12031-80-0

lithium peroxide

terbium(III, IV) oxide

terbium(III, IV) oxide

palladium
7440-05-3

palladium

Li2PdO2

Li2PdO2

Conditions
ConditionsYield
In neat (no solvent) byproducts: Na2TbO3, TbO2; annealing a mixt. of Na2O, Li2O2, and "active" Tb4O7 (Na:Li:Tb = 6:2:1)in a sealed Pd tube (1100°C, 7 d);
lithium peroxide
12031-80-0

lithium peroxide

rubidium oxide

rubidium oxide

arsenic(III) trioxide

arsenic(III) trioxide

2Rb(1+)*Li(1+)*AsO4(3-)=Rb2Li{AsO4}

2Rb(1+)*Li(1+)*AsO4(3-)=Rb2Li{AsO4}

Conditions
ConditionsYield
In neat (no solvent) heating of well-grounded mixtures of the binary oxide, Ni-tube, 550°C, 21d, Ar;; single crystals;;
cesium oxide

cesium oxide

lithium peroxide
12031-80-0

lithium peroxide

arsenic(III) trioxide

arsenic(III) trioxide

2Cs(1+)*Li(1+)*AsO4(3-)=Cs2(Li[AsO4])

2Cs(1+)*Li(1+)*AsO4(3-)=Cs2(Li[AsO4])

Conditions
ConditionsYield
In neat (no solvent) heating of well-grounded mixtures of the binary oxide, Ni-tube, 550°C, 21d, Ar;; single crystals;;
lithium peroxide
12031-80-0

lithium peroxide

potassium oxo cerate (III)

potassium oxo cerate (III)

octalithium oxo cerate (IV)

octalithium oxo cerate (IV)

Conditions
ConditionsYield
In neat (no solvent) byproducts: K2O; annealing a mixt. of Li2O2, and KCeO2 (Li:K:Ce = 9:1:1) in a sealed butnot complete tight Ag bomb tube (sealed in a Supremax glass tube, 650°C, 63 d or <600°C, 90 d);
lithium peroxide
12031-80-0

lithium peroxide

rubidium oxide

rubidium oxide

terbium(III, IV) oxide

terbium(III, IV) oxide

Li6Tb2O7

Li6Tb2O7

Conditions
ConditionsYield
In neat (no solvent) heating (sealed Au tube, 750°C, 13 d or 850°C, 22 d);

12031-80-0Related news

Morphology control of Lithium peroxide (cas 12031-80-0) using Pd3Co as an additive in aprotic Li-O2 batteries07/27/2019

During discharge in aprotic Li-O2 batteries, lithium peroxide (Li2O2) can be formed by a surface- or solution-mediated route. In the surface-mediated process, a Li2O2 film is formed electrochemically on the cathode surface, leading to low capacity and rate capability. In contrast, in high donor ...detailed

12031-80-0Relevant articles and documents

Thermal decomposition study on Li2O2 for Li2NiO2 synthesis as a sacrificing positive additive of lithium-ion batteries

Kim, Jaekwang,Kang, Hyunchul,Hwang, Keebum,Yoon, Songhun

, (2019)

Herein, thermal decomposition experiments of lithium peroxide (Li2O2) were performed to prepare a precursor (Li2O) for sacrificing cathode material, Li2NiO2. The Li2O2 was prepared by a hydrometallurgical reaction between LiOH·H2O and H2O2. The overall reaction during annealing was found to involve the following three steps: (1) dehydration of LiOH·H2O, (2) decomposition of Li2O2, and (3) pyrolysis of the remaining anhydrous LiOH. This stepwise reaction was elucidated by thermal gravimetric and quantitative X-ray diffraction analyses. Furthermore, over-lithiated lithium nickel oxide (Li2NiO2) using our lithium precursor was synthesized, which exhibited a larger yield of 90.9% and higher irreversible capacity of 261 to 265 mAh g?1 than the sample prepared by commercially purchased Li2O (45.6% and 177 to 185 mAh g?1, respectively) due to optimal powder preparation conditions.

Amorphous Li2O2: Chemical Synthesis and Electrochemical Properties

Zhang, Yelong,Cui, Qinghua,Zhang, Xinmin,McKee, William C.,Xu, Ye,Ling, Shigang,Li, Hong,Zhong, Guiming,Yang, Yong,Peng, Zhangquan

, p. 10717 - 10721 (2016)

When aprotic Li–O2batteries discharge, the product phase formed in the cathode often contains two different morphologies, that is, crystalline and amorphous Li2O2. The morphology of Li2O2impacts strongly on the electrochemical performance of Li–O2cells in terms of energy efficiency and rate capability. Crystalline Li2O2is readily available and its properties have been studied in depth for Li–O2batteries. However, little is known about the amorphous Li2O2because of its rarity in high purity. Herein, amorphous Li2O2has been synthesized by a rapid reaction of tetramethylammonium superoxide and LiClO4in solution, and its amorphous nature has been confirmed by a range of techniques. Compared with its crystalline siblings, amorphous Li2O2demonstrates enhanced charge-transport properties and increased electro-oxidation kinetics, manifesting itself a desirable discharge phase for high-performance Li–O2batteries.