Would you expect the tensile strength of polychlorotrifluoroethylene to be greater than, the same as, or less than that of a polytetrafluoroethylene specimen having the same molecular weight and degree of crystallinity? Why?

Short Answer

Expert verified
Answer: Polytetrafluoroethylene (PTFE) is expected to have a higher tensile strength due to the presence of stronger C-F bonds compared to the weaker C-Cl bonds in polychlorotrifluoroethylene (PCTFE).

Step by step solution

01

Compare chemical structures of PCTFE and PTFE

To make a proper comparison, let's first understand the chemical structures of these two polymers: 1. Polychlorotrifluoroethylene (PCTFE) has the formula (-CFCl-CF_2-)_n. It contains both fluorine and chlorine in its structure, which are attached to carbon atoms. 2. Polytetrafluoroethylene (PTFE) has the formula (-CF_2-CF_2-)_n. It solely consists of fluorine atoms attached to carbon atoms.
02

Analyze bond strength in PCTFE and PTFE

Since both polymers have the same molecular weight and degree of crystallinity, the key factor in determining their tensile strength lies in the bond strength present in their respective structures: 1. Fluorine-carbon (C-F) bonds are stronger than chloro-carbon (C-Cl) bonds due to the smaller size and higher electronegativity of fluorine. This means that the C-F bond is more difficult to break compared to the C-Cl bond. 2. In PCTFE, chlorine is relatively larger in size compared to fluorine. This results in weaker bonds and a more flexible structure, which can lead to a decrease in tensile strength.
03

Compare tensile strength of PCTFE and PTFE

Based on the above analysis, we can deduce that the tensile strength of PCTFE will likely be less than that of PTFE. The reason for this is the presence of C-Cl bonds, which are weaker than the C-F bonds present in PTFE, leading to an overall weaker and more flexible polymer structure in PCTFE compared to PTFE. In conclusion, we would expect the tensile strength of polychlorotrifluoroethylene (PCTFE) to be less than that of a polytetrafluoroethylene (PTFE) specimen with the same molecular weight and degree of crystallinity.

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Key Concepts

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

Polychlorotrifluoroethylene (PCTFE)
Polychlorotrifluoroethylene, commonly known by its abbreviation PCTFE, is a thermoplastic polymer notable for its high resistance to chemical attack, excellent moisture barrier properties, and low permeability to gases. It is used in applications that require high resistance to corrosive chemicals and where maintaining a protective barrier is essential. The chemical structure of PCTFE includes chlorine atoms as well as fluorine, which impacts its physical properties compared to polymers that contain only fluorine. Because of the presence of chlorine, PCTFE exhibits different mechanical characteristics, including its tensile strength.

Breaking down the PCTFE structure, we see the alternating chloro-fluoro carbon backbone, which gives it a unique balance between strength and flexibility. Its tensile strength can be affected by factors such as the purity of material or the presence of additives that might impact the polymers' performance in real-world applications.
Polytetrafluoroethylene (PTFE)
Polytetrafluoroethylene, or PTFE, is a synthetic fluoropolymer widely known for its non-stick properties, thermal stability, and a very low coefficient of friction. PTFE, which is often referred to by the brand name Teflon, is composed entirely of carbon and fluorine atoms, leading to a highly stable and strong molecular structure. Its resistance to heat and chemical reactants is largely due to its strong carbon-fluorine bonds, which are considered to be one of the strongest in organic chemistry.

One of the critical features of PTFE is its near-complete resistance to chemical corrosion, making it suitable for use in cookware, industrial pipelines, and medical devices. The strong molecular bonds give PTFE exceptional durability, which is reflected in its tensile strength and makes it an ideal choice for applications that require material with high perseverance under stress.
Molecular Weight
Molecular weight is a fundamental concept in polymer science that plays a crucial role in determining the mechanical properties of polymers, including tensile strength. Mathematically speaking, it is the sum of the atomic weights of all atoms in a molecule. Polymers with a higher molecular weight generally have longer chains, which means more entanglements and stronger intermolecular forces. These characteristics can lead to increased tensile strength, as longer chains take more energy to pull apart.

In comparing PCTFE and PTFE, if we assume they have the same molecular weight, it means the length of their polymer chains is comparable. However, bond strength and structural arrangement will significantly impact their overall mechanical properties, with the identity of these bonds playing a critical role.
Degree of Crystallinity
The degree of crystallinity in polymers refers to the amount of the material's structure that is well-ordered, versus the portion that is amorphous or randomly arranged. A higher degree of crystallinity typically lends to polymers being stiffer, stronger, and more resistant to solvents. Crystalline areas within a polymer contribute to the tensile strength because they are regions where chains are packed tightly in a regular pattern, offering significant resistance to deformation.

For both PCTFE and PTFE, assuming an equal degree of crystallinity implies that the portions of their structures that can align in an orderly manner do so to a similar extent. This alignment significantly affects their mechanical properties, but it's crucial to keep in mind that the presence of chlorine in PCTFE versus only fluorine in PTFE creates dissimilarities in how these regions can form and behave under stress.
Chemical Structure of Polymers
Understanding the chemical structure of polymers is vital to grasp how these materials behave under different conditions. The structure encompasses the arrangement of atoms within the polymer, including the types of bonds present between atoms and the overall spatial arrangement of the polymer chains. Subtle changes in these structures can have pronounced impacts on the polymer's properties, such as melting temperature, solubility, or tensile strength.

Examining the structure of PCTFE and PTFE provides insight into why their tensile strengths differ. Each monomer within PTFE is bonded exclusively with strong carbon-fluorine bonds, while PCTFE has both carbon-fluorine and carbon-chlorine bonds. This distinction in bonding inherently influences the physical properties of the polymers, affecting how they respond when forces are applied to them.
Bond Strength in Polymers
The bond strength in polymers, particularly the strength of carbon-fluorine (C-F) and carbon-chlorine (C-Cl) bonds, is essential in determining their mechanical properties like tensile strength. The bond energy reflects how much energy is needed to break a bond. Carbon-fluorine bonds are among the strongest in organic chemistry due to the small size and high electronegativity of fluorine, which allows for a very stable bond. On the other hand, carbon-chlorine bonds are less strong as chlorine is larger and less electronegative than fluorine.

In the context of PCTFE and PTFE, PTFE's tensile strength benefits from its all C-F bond composition, providing an array of potent bonds throughout the material. These more robust bonds extend the energy required to deform or break the material, rendering it more tensile-strength than PCTFE, which has the inherently weaker C-Cl bonds interspersed within its structure.

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Most popular questions from this chapter

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 strength than the other; (2) if this is possible, note which has the higher tensile strength and then cite the reason(s) for your choice; and (3) if it is not possible to decide, then state why. (a) Linear and isotactic poly(vinyl chloride) with a weight-average molecular weight of \(100,000 \mathrm{g} / \mathrm{mol} ;\) branched and atactic poly \((\) vinyl chloride) having a weight-average molecular weight of \(75,000 \mathrm{g} / \mathrm{mol}\) (b) Graft acrylonitrile-butadiene copolymer with \(10 \%\) of possible sites crosslinked; alternating acrylonitrile-butadiene copolymer with \(5 \%\) of possible sites crosslinked (c) Network polyester; lightly branched polytetrafluoroethylene

For the vulcanization of polyisoprene, compute the weight percent of sulfur that must be added to ensure that \(10 \%\) of possible sites will be crosslinked; assume that, on the average, 3.5 sulfur atoms are associated with each crosslink.

Contrast compression, injection, and transfer molding techniques that are used to form plastic materials.

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 \(150,000 \mathrm{g} / \mathrm{mol}\)

Normal butane and isobutane have boiling temperatures of -0.5 and \(-12.3^{\circ} \mathrm{C}(31.1\) and \(\left.9.9^{\circ} \mathrm{F}\right),\) respectively. Briefly explain this behavior on the basis of their molecular structures, as presented in Section 14.2.

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