List the two molecular characteristics that are essential for elastomers.

Short Answer

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Answer: The two essential molecular characteristics of elastomers are long-chain polymer molecules and cross-linking.

Step by step solution

01

Understanding Elastomers

Elastomers are a type of polymer that can be stretched or deformed and return to their original shape. These materials display unique properties like high elasticity and resilience, which makes them ideal for many applications, such as rubber bands, tires, and seals.
02

Essential Molecular Characteristics of Elastomers

The two molecular characteristics essential for elastomers are: 1. Long-chain polymer molecules: It is important for elastomers to have long, flexible polymer chains. These chains can stretch easily when force is applied and return to their original shape when the force is removed. \[\] 2. Cross-linking: Cross-linking refers to the formation of covalent bonds or other connections between the polymer chains. Cross-linking is crucial for elastomers as it provides network structures that enable elastomers to maintain their structural integrity and mechanical property even when the materials are stretched or deformed. This cross-linking gives the elastomers their unique elastic and resilient properties.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Long-Chain Polymer Molecules
Long-chain polymer molecules are the fundamental structural units of elastomers, providing them with their characteristic stretchability and flexibility. These molecules are chains composed of repeating units called monomers, linked together like a string of beads. Imagine a spaghetti noodle; it's long and can be twirled and twisted, much like the polymer chains that make up an elastomer.

The length of these molecules plays a critical role in how an elastomer behaves. The longer the chains, the more they can extend under tension. This ability to stretch is a result of the molecular segments sliding past each other when force is applied. Once the force is removed, the chains recoil back to their original, entangled state, much like how a relaxed rubber band retracts after being stretched.

It's this interplay of flexibility and retraction in the long polymer chains that permits elastomers to be used in diverse applications, from the soles of your shoes to the seals around your car windows. They are designed to endure significant deformation without breaking, thus serving their purpose effectively in everyday products.
Cross-Linking in Polymers
Cross-linking in polymers is a chemical process that significantly affects the elastomers' mechanical properties. If we go back to the spaghetti analogy, cross-linking would be like placing random spots of glue between the noodles. The noodles could still move, but they would be connected at various points, providing a limited structure to the otherwise chaotic tangle.

In elastomers, cross-links are connections between the long polymer chains, which restrict their motion to a certain extent; this is crucial for the material to 'snap back' to its original form. These links can be formed via covalent bonds, which are strong and permanent, or through weaker, reversible interactions like hydrogen bonds or ionic interactions.

Cross-linking is what makes the difference between a liquid plastic that flows freely and the tough, resilient properties of a rubber band. The density and type of cross-links can be altered to fine-tune the elastomer's properties, adjusting its hardness, elasticity, and resistance to chemicals and temperature. Understanding the relationship between cross-linking and the properties of the material is essential in designing elastomers for specific applications.
Elasticity and Resilience of Elastomers
Elasticity and resilience are the hallmark traits of elastomers, allowing them to be deformed and then return to their original shape without permanent damage. These properties go hand in hand, but they are not the same. Elasticity is the ability of a material to stretch and change shape when a force is applied. A material must be able to stretch to be elastic, but how well the material can return to its original state after being deformed is a measure of its resilience.

Imagine pressing a ball made of soft clay versus one made of rubber. The clay might change shape easily (showing it's malleable), but it won't bounce back like the rubber ball. This difference illustrates resilience; the rubber ball has higher resilience than the clay.

The resilience of elastomers comes from their molecular makeup—long-chain molecules bound by cross-links. These features enable elastomers to absorb and dissipate energy from impacts or deformations, making them ideal for shock absorbers and vibration dampeners. By carefully balancing the degree of cross-linking and the flexibility of the polymer chains, manufacturers create materials that can withstand various degrees of stress, from the soft rubber of a silicone spatula to the firm, durable tire of a car.

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Most popular questions from this chapter

The tensile strength and number-average molecular weight for two polyethylene materials are as follows: Estimate the number-average molecular weight that is required to give a tensile strength of \(140 \mathrm{MPa}\).

For thermoplastic polymers, cite five factors that favor brittle fracture.

For each of the following pairs of polymers, do the following: (1) state whether or not it is possible to decide whether one polymer has a higher tensile modulus than the other; (2) if this is possible, note which has the higher tensile modulus and then cite the reason(s) for your choice; and (3) if it is not possible to decide, then state why. (a) Branched and atactic poly(vinyl chloride) with a weight-average molecular weight of \(100,000 \mathrm{g} / \mathrm{mol} ;\) linear and isotactic poly \((\) vinyl chloride) having a weight-average molecular weight of \(75,000 \mathrm{g} / \mathrm{mol}\) (b) Random styrene-butadiene copolymer with \(5 \%\) of possible sites crosslinked; block styrene-butadiene copolymer with \(10 \%\) of possible sites crosslinked (c) Branched polyethylene with a numberaverage molecular weight of \(100,000 \mathrm{g} / \mathrm{mol}\) atactic polypropylene with a number-average molecular weight of \(150,000 \mathrm{g} / \mathrm{mol}\)

Briefly explain the difference in molecular chemistry between silicone polymers and other polymeric materials.

For each of the following pairs of polymers plot and label schematic specific volume versus temperature curves on the same graph (i.e., make separate plots for parts a, b, and c). (a) Linear polyethylene with a weightaverage molecular weight of \(75,000 \mathrm{g} / \mathrm{mol}\); branched polyethylene with a weightaverage molecular weight of \(50,000 \mathrm{g} / \mathrm{mol}\) (b) Spherulitic poly(vinyl chloride), of \(50 \%\) crystallinity, and having a degree of polymerization of \(5000 ;\) spherulitic polypropylene, of \(50 \%\) crystallinity, and degree of polymerization of 10,000 (c) Totally amorphous polystyrene having a degree of polymerization of \(7000 ;\) totally amorphous polypropylene having a degree of polymerization of 7000

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