Dicumyl peroxide: Difference between revisions
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{{DISPLAYTITLE:Dicumyl peroxide}} | |||
== | == Overview == | ||
Dicumyl peroxide | [[File:Dicumyl_peroxide.svg|thumb|right|Structural formula of dicumyl peroxide]] | ||
'''Dicumyl peroxide''' is an organic compound with the formula (C_H_C(CH_)_O)_. It is a white crystalline solid that is used as a [[radical initiator]] in the polymerization of [[styrene]], [[acrylics]], and [[polyethylene]]. | |||
== | == Chemical Structure == | ||
Dicumyl peroxide is a [[peroxide]], which means it contains a peroxide group (_O_O_) in its structure. The compound consists of two cumyl groups (C_H_C(CH_)_) connected by a peroxide linkage. This structure is responsible for its ability to decompose and generate free radicals, which are essential in initiating polymerization reactions. | |||
== Applications == | |||
Dicumyl peroxide is widely used in the [[plastics]] and [[rubber]] industries. It serves as a cross-linking agent for [[polyethylene]] and [[polypropylene]], improving the mechanical properties and thermal stability of these materials. In the production of [[polystyrene]], dicumyl peroxide acts as a [[catalyst]] to initiate the polymerization process. | |||
==Safety== | == Safety and Handling == | ||
As with many peroxides, dicumyl peroxide is a [[hazardous material]] and must be handled with care. It is a strong oxidizing agent and can pose a risk of explosion if not stored properly. Safety measures include storing it in a cool, dry place away from [[reducing agents]] and [[flammable materials]]. | |||
== | == Decomposition == | ||
Upon heating, dicumyl peroxide decomposes to form acetophenone and methane, along with free radicals. This decomposition is exothermic and is the basis for its use as a radical initiator. The decomposition temperature is a critical parameter in its application, as it determines the onset of radical generation. | |||
== Related Compounds == | |||
* [[Benzoyl peroxide]] | |||
* [[Tert-butyl hydroperoxide]] | |||
* [[Cumene hydroperoxide]] | |||
== Related Pages == | |||
* [[Polymer chemistry]] | |||
* [[Free radical polymerization]] | |||
* [[Cross-linking]] | |||
[[Category:Organic peroxides]] | [[Category:Organic peroxides]] | ||
[[Category:Polymer chemistry]] | |||
Latest revision as of 11:31, 15 February 2025
Overview[edit]

Dicumyl peroxide is an organic compound with the formula (C_H_C(CH_)_O)_. It is a white crystalline solid that is used as a radical initiator in the polymerization of styrene, acrylics, and polyethylene.
Chemical Structure[edit]
Dicumyl peroxide is a peroxide, which means it contains a peroxide group (_O_O_) in its structure. The compound consists of two cumyl groups (C_H_C(CH_)_) connected by a peroxide linkage. This structure is responsible for its ability to decompose and generate free radicals, which are essential in initiating polymerization reactions.
Applications[edit]
Dicumyl peroxide is widely used in the plastics and rubber industries. It serves as a cross-linking agent for polyethylene and polypropylene, improving the mechanical properties and thermal stability of these materials. In the production of polystyrene, dicumyl peroxide acts as a catalyst to initiate the polymerization process.
Safety and Handling[edit]
As with many peroxides, dicumyl peroxide is a hazardous material and must be handled with care. It is a strong oxidizing agent and can pose a risk of explosion if not stored properly. Safety measures include storing it in a cool, dry place away from reducing agents and flammable materials.
Decomposition[edit]
Upon heating, dicumyl peroxide decomposes to form acetophenone and methane, along with free radicals. This decomposition is exothermic and is the basis for its use as a radical initiator. The decomposition temperature is a critical parameter in its application, as it determines the onset of radical generation.