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1313-60-6

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1313-60-6 Usage

Preparation

Although sodium peroxide, Na202, is the principal product of the combustion of sodium, sodium monoxide is prepared commercially by carefully permitting sodium to react with a limited amount of oxygen according to the equation? If the sodium monoxide thus prepared is exposed to further dry oxygen or air, it is oxidized to the peroxide; this is the commercial method of preparing Na202 , the most important alkali peroxide,

Description

Sodium peroxide has a molecular formula of Na2O2 and is an inorganic peroxide salt. It is a yellowish-white powder that turns yellow when heated. Sodium peroxide absorbs water and carbon dioxide from the air and is soluble in cold water. It is a strong oxidizing agent, is corrosive and can cause burns to the eyes and skin, and is also toxic by ingestion and inhalation. Sodium peroxide is water reactive and a dangerous fire and explosion risk in contact with water, alcohol, or acids. Sodium peroxide forms self-igniting mixtures with powdered metals and organic materials. It is incompatible with ethyl or methyl alcohol, glacial acetic acid, carbon disulfide, glycerin, ethylene glycol, and ethyl acetate. The four-digit UN identification number is 1504. The NFPA 704 designation is health 3, flammability 0, and reactivity 1. The 704 diamond has the prefix “oxy” in the white space at the bottom. It is used as bleach and as an oxygen-generating material for diving bells and submarines.

Chemical Properties

Different sources of media describe the Chemical Properties of 1313-60-6 differently. You can refer to the following data:
1. Sodium peroxide, Na2O2, is a pale yellow solid, stable at ambient temperature, and hygroscopic. On heating, it starts to liberate oxygen at about 300 °C and decomposes rapidly above its melting point of 460 °C.
2. Sodium peroxide, Na202, is a fire-hazardous white powder that yellows when heated and causes ignition when in contact with water. Sodium peroxide is decomposed by heating, although this is not easily accomplished. It is stable in dry air; however, in moist air,or when acted on by water, it decomposes readily. It can be a powerful oxidizer and a powerful reducing agent, depending on conditions. Sodium peroxide is also used as a bleach, in medicine soap, and in the decomposition of minerals.

Uses

Different sources of media describe the Uses of 1313-60-6 differently. You can refer to the following data:
1. Bleaching animal and vegetable fibers, feathers, bones, ivory, wood, wax, sponges, coral; rendering air charged with CO2 respirable as in torpedo boats, submarines, diving bells, etc.; purifying air in sick rooms; dyeing and printing textiles; chemical analysis. General oxidizing agent.
2. As an oxidizing agent, a bleaching agent, deodorant, pharmaceuticals and dyes, and as an analytical reagent.Sodium peroxide acts as a bleaching agent in laundry and wood pulp. It finds application in the extraction of minerals from various ores. It acts as an oxidizing agent as well as an oxygen source by reacting with carbon dioxide. Furthermore, it is used as a deodorant and an analytical reagent. It is also useful in scuba gear and in submarines.
3. Sodium peroxide historically was used to bleach wood pulp for the production of paper and textiles. It is mainly used for specialized laboratory operations, for example, the extraction of minerals from various ores. Sodium peroxide is used as an oxidizing agent and is used as an oxygen source by reacting with carbon dioxide to produce oxygen and sodium carbonate; it is thus particularly useful in scuba gear, submarines, and so on.

Definition

Different sources of media describe the Definition of 1313-60-6 differently. You can refer to the following data:
1. sodium peroxide: A whitish solid(yellow when hot), Na2O2, soluble inice-water and decomposed in warmwater or alcohol; r.d. 2.80; decomposesat 460°C. A crystalline octahydrate(hexagonal) is obtained bycrystallization from ice-water. Thecompound is formed by the combustionof sodium metal in excess oxygen.At normal temperatures itreacts with water to give sodiumhydroxide and hydrogen peroxide.It is a powerful oxidizing agent reactingwith iodine vapour to give theiodate and periodate, with carbon at300°C to give the carbonate, andwith nitrogen(II) oxide to give thenitrate. It is used as a bleachingagent in wool and yarn processing,in the refining of oils and fats, andin the production of wood pulp.
2. Exists as impurity (about 10%) in sodium peroxide, obtained by heat- ing sodium peroxide in oxygen, reacts with water to yield hydrogen peroxide, oxygen, and sodium hydroxide.

General Description

A yellow-white to yellow granular solid. Mixtures with combustible material are readily ignited by friction, heat, or contact with moisture. May vigorously decompose under prolonged exposure to heat, causing the rupture of the containers.

Air & Water Reactions

Reacts vigorously with water, large amounts react explosively [Haz. Chem. Data 1969. p. 201].

Reactivity Profile

Sodium peroxide reacts violently with reducing agents, combustible materials and light metals. Reacts exothermically and rapidly or even explosively with water to form a strong base (NaOH) and oxygen (O2) [Handling Chemicals Safely 1980 p. 854]. A mixture with ammonium persulfate can explode if subjected to friction (crushing in a mortar), if heated, or if a stream of gaseous carbon dioxide is passed over Sodium peroxide [Mellor 10:464 1946-47]. Reacts very vigorously with gaseous hydrogen sulfide; even in the absence of air, the reaction may be accompanied by flame [Mellor 10:132 1946-47]. An explosion results when gaseous carbon dioxide is passed over a mixture of Sodium peroxide with powdered magnesium [Mellor 2:490 1946-47] . Mixtures with acetic acid or acetic anhydride can explode if not kept cold [Von Schwartz 1918 p. 321]. Spontaneously flammable in contact with aniline, benzene, diethyl ether, or organic materials such as paper and wood. Mixtures with charcoal, glycerine, certain oils, and phosphorus burn or explode [Mellor 2:490 1946-47]. A mixture with calcium carbide (powdered) burst into flame when exposed to damp air and exploded when heated [Mellor 2:490 1946-47]. Decomposes, often violently in the presence of catalytic quantities of manganese dioxide [Mellor 2 Supp. 2:635 1961]. Mixing with sulfur monochloride leads to a violent reaction [Mellor 2 Supp. 2:634 1961]. Can react with and cause the ignition of fuels.

Hazard

Dangerous fire and explosion risk in contact with water, alcohols, acids, powdered metals, and organic materials. Strong oxidizing agent. Keep dry. Irritant.

Health Hazard

TOXIC; inhalation or contact with vapor, substance, or decomposition products may cause severe injury or death. Fire will produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may cause pollution.

Fire Hazard

May ignite combustibles (wood, paper, oil, clothing, etc.). React vigorously and/or explosively with water. Produce toxic and/or corrosive substances on contact with water. Flammable/toxic gases may accumulate in tanks and hopper cars. Some may produce flammable hydrogen gas upon contact with metals. Containers may explode when heated. Runoff may create fire or explosion hazard.

Flammability and Explosibility

Notclassified

Safety Profile

A severe irritant to shin, eyes, and mucous membranes. Dangerous fire hazard by chemical reaction; a powerfuloxidizing agent. Reacts explosively or violently under the appropriate conditions with water, acids, powdered metals, acetic acid, acetic anhydride, Al, (Al + CO2), aluminum + aluminum chloride, almond oil, (NH4)2S208, aniline, Sb, As, benzene, boron nitride, calcium aceqlide, charcoal, Cu, cotton wool, (KNO3 + dextrose), diethyl ether, fibrous materials + water, glucose + potassium nitrate, hexamethylene-tetramine, hydrogen sulfide, hydroxy compounds (e.g., ethanol, ethylene glycol, glycerol, sugar), magnesium, (Mg + CO2), MnO2, metals, metals + carbon dioxide + water, nonmetals (e.g., carbon, phosphorus, antimony, arsenic, boron, sulfur, selenium), nonmetal halides (e.g., diselenium dichloride, disulfur dichloride, phosphorus trichloride), organic matter, paraffin, K, silver chloride + charcoal, soap, Na, sodium dioxide, SCl, Sn, Zn, wood, peroxyformic acid, reducing materials. Will react with water or steam to produce heat and toxic fumes. To fight fire, use carbon dioxide or dry chemical. Combustible materials ignited by contact with sodium peroxide should be smothered with soda ash, salt or dolomite mixtures. Chemical fire extinguishers should not be used. If the fire cannot be smothered, it should be flooded with large quantities of water from a hose. When heated to decomposition it emits toxic fumes of Na2O. See also SODIUM HYDROXIDE and PEROXIDES, INORGANIC.

Check Digit Verification of cas no

The CAS Registry Mumber 1313-60-6 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 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1313-60:
(6*1)+(5*3)+(4*1)+(3*3)+(2*6)+(1*0)=46
46 % 10 = 6
So 1313-60-6 is a valid CAS Registry Number.
InChI:InChI=1/2Na.O2/c;;1-2/q2*+1;-2/rNa2O2/c1-3-4-2

1313-60-6SDS

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 Sodium peroxide

1.2 Other means of identification

Product number -
Other names disodium,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:1313-60-6 SDS

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A protocol based on peroxide fusion has been developed for the determination of Au in metallurgical samples and ores covering a wide range of concentrations and diverse mineralogies. The quantity of Na2O2 required was minimised, while maintaining lixiviant efficacy, by the use of mixed NaOH + Na...detailed