Chapter 25: Problem 94
Describe the formation of polystyrene.
Short Answer
Expert verified
Polystyrene forms through radical polymerization of styrene monomers.
Step by step solution
01
Introduction to Monomer
Polystyrene is formed from the monomer styrene. Styrene is an organic compound with the chemical formula \(C_8H_8\), which consists of an ethylene molecule (\(C_2H_4\)) with a phenyl group (\(C_6H_5\)) attached.
02
Initiation of Polymerization
The formation of polystyrene begins through a process called polymerization. Specifically, a type known as radical polymerization is used. This involves initiating the reaction by breaking the double bond in the styrene monomer, typically using a radical initiator like benzoyl peroxide.
03
Chain Propagation
Once initiation starts, the free radicals generated react with the double bonds of other styrene monomers. Each styrene adds to the growing chain, which lengthens and forms a polymer chain while the radical transfers to the end of the chain.
04
Termination of Polymerization
The polymerization process terminates when two growing polymer chains combine or when the free radical is quenched. This step stops the growth of the polymer chains, yielding solid polystyrene material.
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Monomer Styrene
The journey to forming polystyrene begins with its fundamental building block, the monomer styrene. Styrene is a small organic compound that consists of a vinyl group attached to a benzene ring, with its chemical formula being \( C_8H_8 \). This structure can be further broken down to show that it comprises an ethylene molecule (\( C_2H_4 \)) bonded to a phenyl group (\( C_6H_5 \)). By understanding these components, we can appreciate how styrene monomers are uniquely structured to create long polymer chains that eventually form polystyrene.
Styrene itself is a liquid at room temperature and has the distinctive property of being able to undergo a chemical reaction that breaks its double bonds. This ability to participate in such reactions makes it highly susceptible to polymerization processes, where it can join with other styrene monomers in a repeating pattern to form a larger material like polystyrene.
Styrene itself is a liquid at room temperature and has the distinctive property of being able to undergo a chemical reaction that breaks its double bonds. This ability to participate in such reactions makes it highly susceptible to polymerization processes, where it can join with other styrene monomers in a repeating pattern to form a larger material like polystyrene.
Radical Polymerization
Radical polymerization is the primary process used in the formation of polystyrene. This method of polymerization relies on the presence of free radicals, which are molecules with unpaired electrons. These radicals are highly reactive and can initiate the breaking of double bonds in styrene. For radical polymerization to start, a radical initiator such as benzoyl peroxide is typically used.
When benzoyl peroxide is introduced, it decomposes upon heating to produce free radicals. These radicals then attack the double bond in the styrene monomer, creating new radicals as the double bond breaks. This chain of reactions continues, resulting in a polymerizing effect where new radicals are constantly being generated to react with more styrene monomers. Thus, radical polymerization sets the stage for the growth of polymer chains that constitute polystyrene.
When benzoyl peroxide is introduced, it decomposes upon heating to produce free radicals. These radicals then attack the double bond in the styrene monomer, creating new radicals as the double bond breaks. This chain of reactions continues, resulting in a polymerizing effect where new radicals are constantly being generated to react with more styrene monomers. Thus, radical polymerization sets the stage for the growth of polymer chains that constitute polystyrene.
- Radicals initiate the reaction by breaking double bonds.
- Radical initiators like benzoyl peroxide are commonly used.
- The process is characterized by high reactivity and rapid progression.
Polymer Chain Propagation
During the polymerization of styrene, the stage known as chain propagation is where the real action takes place. After the initial activation by a radical, the newly formed radical at the end of the growing chain reacts with adjacent styrene monomers. This reaction continues to add more styrene units to the chain.
The fascinating part of chain propagation is how each monomer addition retains the radical at the chain's end. This allows the chain to continue growing with each successive reaction with other styrene molecules. This chain reaction is both rapid and self-propagating, forming long chains of polymerized styrene. As each new styrene is added, the radical simply transfers to the new end of the chain, enabling continuous growth.
The fascinating part of chain propagation is how each monomer addition retains the radical at the chain's end. This allows the chain to continue growing with each successive reaction with other styrene molecules. This chain reaction is both rapid and self-propagating, forming long chains of polymerized styrene. As each new styrene is added, the radical simply transfers to the new end of the chain, enabling continuous growth.
- Each styrene monomer is added to the chain, lengthening it.
- The radical moves to the new chain end, allowing further addition.
- Propagation is a repeating cycle, resulting in long polymer chains.
Polymerization Termination
The polymerization process doesn't continue indefinitely; it is eventually brought to a halt through a process called termination. Termination occurs when the growth of polymer chains stops, often due to the recombination of two radicalized polymer ends or when a radical is quenched.
This cessation of growth can happen in several ways, such as through combination or disproportionation. In combination termination, two polymer radicals might meet and bond together, eliminating the free radicals and stabilizing the structure of both chains. Alternatively, disproportionation may occur when the radical transfers its activity to another molecule.
This cessation of growth can happen in several ways, such as through combination or disproportionation. In combination termination, two polymer radicals might meet and bond together, eliminating the free radicals and stabilizing the structure of both chains. Alternatively, disproportionation may occur when the radical transfers its activity to another molecule.
- Termination halts chain growth and solidifies polystyrene.
- Combination involves the joining of two chain ends.
- Disproportionation involves radical transfer to a different atom or molecule.