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1314-18-7

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1314-18-7 Usage

Uses

Different sources of media describe the Uses of 1314-18-7 differently. You can refer to the following data:
1. Strontium dioxide (SrO2) can cause fires or explode when heated and in contact with organic substances. It is used as both a reducing agent and an oxidizing agent.
2. Strontium peroxide or strontium dioxide (SrO2) can cause fires or explode when heated and in contact with organic substances. It is used as both a reducing agent and an oxidizing agent.
3. Strontium Peroxide is an oxidizing agent that is used for bleaching. It has also been used in some pyrotechnic displays to provide a vivid-red color.
4. The only substantial application for this compound is in pyrotechnics. Strontium peroxide produces a red color in flames.

Chemical Properties

Different sources of media describe the Chemical Properties of 1314-18-7 differently. You can refer to the following data:
1. Strontium peroxide is a lightcolored solid of good thermal stability. Commercial strontium peroxide contains about 85% SrO2 and 10% active oxygen.
2. white to off-white powder

Preparation

Like the other alkaline earth peroxides, it can be prepared by reaction of the nitrate and sodium peroxide in a cold solution: Sr(NO3)2+ Na2O2+xH2OSrO2·xH2O+2NaNO3 The hydrated form is usually the octahydrate. If the anhydrate is desired, the hydrated peroxide is dried and then sintered at 350°C for 10 min or less: SrO2·xH2O+ heat→SrO+SrO2+H2O

General Description

A white powder. Insoluble in water and slowly decomposed by water. Noncombustible, but accelerates the burning of combustible material.

Air & Water Reactions

Insoluble in water and slowly decomposed by water.

Reactivity Profile

Strontium peroxide may explode from friction, heat or contamination. Accelerates burning when involved in a fire. May ignite combustibles (wood, paper, oil, clothing, etc.). If the combustible material is finely divided the mixture may be explosive.

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. A skin, eye, and mucous membrane irritant. Mixtures with organic materials readily ignite with friction or on contact with moisture. See also PEROXIDES and STRONTIUM COMPOUNDS.

Check Digit Verification of cas no

The CAS Registry Mumber 1314-18-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,3,1 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1314-18:
(6*1)+(5*3)+(4*1)+(3*4)+(2*1)+(1*8)=47
47 % 10 = 7
So 1314-18-7 is a valid CAS Registry Number.
InChI:InChI=1/O2.Sr/c1-2;/q-2;+2

1314-18-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name strontium,peroxide

1.2 Other means of identification

Product number -
Other names strontium peroxide

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:1314-18-7 SDS

1314-18-7Relevant articles and documents

High-pressure synthesis of perovskite-derived compounds in the Sr-Y-Cu-O system

Ono Akira

, (1992)

Three perovskite-derived compounds were found in the Sr-Y-Cu-O system treated at 1.6 GPa. These are Sr3Cu8O2, Sr3.5Y1.5Cu3O2 and Sr4Y3Cu4O14. These compounds are high-pressure phases crystallized in orthorhombic structures. The stabilities of the new compounds depended highly on oxygen pressure. The non-superconducting orthorhombic phase Sr2YCu3O2 was also discovered: It was obtained at a relatively low oxygen pressure. Magnetic susceptibility measurements have revealed that the superconducting transition temperature of Sr2YCu3O2 decreased on lowering the oxygen content.

New series of high-Tc superconductors AlSr2Can-1CunO2n+3 (n = 4, Tc = 110 K; n = 5, Tc = 83 K) prepared at high pressure

Isobe,Kawashima,Kosuda,Matsui,Takayama-Muromachi

, p. 120 - 126 (1994)

A new series of high-Tc superconductors AlSr2Can-1CunO2n+3 (Al-12(n - 1)n) was prepared at high pressure of 5.5 GPa and 1250°C, whose members are the first superconductors including Al as a main component. Two members with n = 4, 5 were obtained in bulk and the former showed superconducting transition at 110 K while the latter at 83 K. They had tetragonal cells with a = 3.839(1), c = 17.72(1) angstrom for n = 4 and a = 3.845(1), c = 20.87(1) angstrom for n = 5. HRTEM observations indicated that they are essentially isomorphous with the Tl (or Hg)-based superconductors, Tl (Hg)-1234 and 1245, respectively. Significant intergrowths of phases with different n values up to n = 8 were observed in Al-1245.

High-pressure synthesis and magnetic properties of the niobio-cuprate Nb0.9Sr2HoCu2.1O7.9

Balamurugan,Yamaura,Takayama-Muromachi

, p. 1206 - 1209 (2008)

Ho-based 1212 niobio-cuprate (Nb-1212Ho) was synthesized for the first time. An off-stoichiometric starting composition Nb0.9Sr2HoCu2.1O7.9 led a phase-pure polycrystalline sample under the synthesis condition at 1450 °C for 2 h at 6 GPa, approximating the true bulk composition. X-ray diffraction pattern clearly indicated an Nb-1212 type structure for the compound with lattice parameters a = b = 3.8505(1) A? and c = 11.574(3) A?, suggesting that the space group P4/mmm is likely for the structure. Unlike Nb-1212Y, the Nb-1212Ho compound showed neither superconductivity nor a magnetic order down to 1.8 K. A relatively large magneto-resistance approximately -7% was found at 30 K.

High-pressure synthesis of the zero-charge-reservoir 0223 superconductor in the Sr-Ca-Cu-O system

Ushiki, Masako,Motohashi, Teruki,Yamauchi, Hisao,Karppinen, Maarit

, p. 167 - 172 (2002)

We have refined the high-pressure synthesis of the zero-charge-reservoir 0223 phase of the Sr-Ca-Cu-O system. Samples were prepared from three different starting cation compositions of Sr2CaCu2O6+y, Sr2Ca2Cu3O8+y and Sr2Ca3Cu4O10+y. The amount of oxygen, y, was controlled by using different amounts of SrO2 in the starting material mixture. With SrO2 of commercial grade, two types of HRTEM images were observed for the a-b plane: one with a double periodicity and another with no periodicity. TEM-EELS analysis revealed that the former was due to carbonate inclusions. Using freshly synthesized SrO2, crystalline samples with Tc ≈ 110 K were obtained. The samples showed body-centered symmetry in ED patterns, being thus of the 0(Sr)2(Ca)23 phase. The actual amount of oxygen in the obtained samples as determined by wet-chemical analysis was found considerably lower than the nominal value. However, the wet-chemical analysis revealed a much higher oxidation state for the 0(Sr)2(Ca)23 phase than generally expected for a high-Tc superconductor.

New oxyfluoride superconductors Sr2Can-1CunO2n+δF2±y (n = 2; Tc = 99 K, n = 3; Tc = 111 K) prepared at high pressure

Kawashima,Matsui,Takayama-Muromachi

, p. 313 - 320 (1996)

We prepared new oxyfluoride superconductors, Sr2CaCu2O4+δF2±y and Sr2Ca2Cu3O6+δF2±y, at 1250 °C under 5.5 GPa. These phases are the n = 2, 3 members of a homologous series, Sr2Can-1CunO2n+δF2±y, respectively, in which the n = 1 phase was reported previously. X-ray and HRTEM studies indicated that they have tetragonal structures with a = 3.843(1), c = 19.88(1) angstroms for n = 2 and a = 3.840(1), c = 26.17(1) angstroms for n = 3. The n = 2 phase showed a superconducting transition at 99 K, while the n = 3 one at 111 K.