BME213 Sem 3 Flashcards

1
Q

Compare the two synthesis methods. Give an example of polymer synthesized via each method.

A
  1. Addition Polymerization (Chain-Growth):
    • Monomers with double bonds join without forming by-products.
    • Uses free radicals or ions to start the chain reaction.
    • Fast growth, typically one type of monomer.
    • Example: Polyethylene (from ethene)
  2. Condensation Polymerization (Step-Growth):
    • Monomers with two functional groups react step-by-step.
    • Produces small by-products (like water or HCl).
    • Slower build-up, often involves two types of monomers.
    • Example: Nylon-6,6 (from hexamethylene diamine and adipic acid)
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2
Q

What key marker would you use to decide which polymerization mechanism a monomer would use?

A

The type of functional group or bond present in the monomer is the key marker.

If the monomer has:
• A carbon-carbon double bond (C=C) → It will likely undergo addition polymerization.
• Example: Ethene → Polyethylene
• Two or more reactive functional groups (e.g., –OH, –COOH, –NH₂) → It will undergo condensation polymerization.
• Example: Adipic acid + Hexamethylene diamine → Nylon-6,6

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3
Q

Addition polymerization has 3 steps. Briefly explain each stepusing ethene as the monomer.

A
  1. Initiation:
    • A free radical (e.g. from a peroxide) attacks ethene’s double bond, breaking it and creating a reactive chain-starting radical.
    • Example:
    R + CH2 = CH2 -> RCH2CH2
  2. Propagation:
    • The active chain end reacts with more ethene monomers, growing the polymer.
    • Example:
    RCH2CH2 + CH2 = CH2 -> RCH2CH2CH2CH2
  3. Termination:
    • Two growing chains (radicals) combine, ending the chain reaction.
    • polymerization comes to a stop via 2 principle mechanisms:
    - recombination : joining of 2 radial molecules to form a non-reactive molecule
    - occlusion : “frozen mobility” caused by decrease mobility of free radicals, macro-radicals and monomers due to entrapment within the increasingly dense polymer structure
    • Example:
    CH2CH2 + CH2CH2 -> CH2CH2CH2CH2
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4
Q

Draw the reaction mechanism for the polymerization of Nylon 6,6. Are there any by-products produced?

A

Reaction Mechanism (in words):
• Hexamethylene diamine (H₂N–(CH₂)₆–NH₂) reacts with adipic acid (HOOC–(CH₂)₄–COOH).
• An amide bond (–CO–NH–) is formed between the –NH₂ and –COOH groups.
• This repeats to form a long-chain polymer:
–NH–(CH₂)₆–NH–CO–(CH₂)₄–CO– \text{ (repeating unit)}

By-Product:
• Yes — water (H₂O) is released each time a bond forms.
• This is typical of condensation polymerization.

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5
Q

What are the classification of polymers by structure?

A
  1. Linear Polymers
    • Long, straight chains (no branches or cross-links)
    • Example: Polyethylene, PVC
  2. Branched Polymers
    • Main chain with short side branches
    • Example: Low-Density Polyethylene (LDPE)
  3. Cross-linked Polymers
    • Chains connected by covalent bonds (cross-links)
    • Rigid and thermosetting
    • Example: Bakelite, vulcanized rubber
  4. Network Polymers
    • Extensive 3D bonding between monomers
    • Very hard and brittle
    • Example: Epoxy resin, phenol-formaldehyde
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6
Q

What are the different between thermoplastics and thermosets polymers?

A

Thermoplastics
• Soften when heated, can be remolded repeatedly
• Have linear or branched structures
• No cross-links between chains
• Recyclable
• Example: Polyethylene, PVC, Polystyrene

Thermosets (Thermosetting Polymers)
• Harden permanently when heated — cannot be remelted
• Have extensive cross-linking between chains
• Rigid and heat-resistant
• Not recyclable
• Example: Bakelite, Epoxy resin, Melamine

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7
Q

Describe the 2 types of bonding found in polymers

A
  1. Primary Bonding (Covalent Bonds)
    • Strong bonds that hold atoms together within each polymer chain
    • Formed during polymerization
    • Provide backbone strength to the polymer
    • Example: Carbon-carbon bonds in polyethylene
  2. Secondary Bonding (Intermolecular Forces)
    • Weaker forces between different polymer chains
    • Include van der Waals forces, hydrogen bonds, or dipole interactions
    • Influence properties like flexibility, melting point, and solubility
    • Example: Hydrogen bonding between chains in nylon
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8
Q

What are 5 Advantages of Polymers

A
  1. Lower material cost compared to other biomaterials.
  2. Ease of manufacturability to produce various shapes
    including complex shapes, e.g bulk, film, sheet, fibres, etc
  3. Wide range of physical and mechanical properties (variety
    of density and molecular weight).
  4. Easily shaped or modified by the surgeon in-situ to obtain
    better fitting.
  5. Polymer is organic, higher biocompatibility compared to
    other class of materials and low thrombocytes
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9
Q

What is a “polymer”?

A

A long chain macromolecule made up of many repeating units. Can often contain as many 45,000 repeating units.

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10
Q

What is a “monomer”?

A

The small repeating unit used to make up the polymer. E.g. ethene in polyethene

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11
Q

What is a “biopolymer”?

A

A biopolymer is a polymer that can be used for creating biomedical devices that come into contact with human biological
tissue or fluids.

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12
Q

What is a monomer’s functionality?

A

The number of bonding sites a monomer has with other monomer.

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