1a MPK---Structure of polymers.pdf

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    The Structure of Polymers

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    What is a polymer?

    made up from lots of

    small moleculescalled monomers.

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    All the same monomer

    Monomers all sametype (A)

    A + A + A + A

    -A-A-A-A-

    eg poly(ethene)

    polychloroethene

    PVC

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    Copolymerisation

    Copolymerisation occurs when more thanone monomeris used.

    An irregular chain structure will result eg

    ro ene/ethene/ ro ene/ ro ene/ethene

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    The Structure of Polymers

    Polymers are created by the chemical

    These polymers are specifically made of

    .

    Carbon makes up the backbone of the

    bonded along the carbon backbone.

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    The Structure of Polymers

    Polymers that contain primarily carbon andhydrogen are classified as organic

    polymers.

    Polypropylene and polystyrene are exampleso t ese.

    Even though the basic makeup of many

    po ymers s car on an y rogen, o erelements can also be involved.

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    The Structure of Polymers

    Oxygen, chlorine, fluorine, nitrogen, silicon,phosphorous and sulfur are other elements

    that are found in the molecular makeup of

    polymers. o yv ny c or e conta ns c or ne.

    Nylon contains nitrogen.

    Teflon contains fluorine. Polyester and polycarbonates contain

    oxygen.

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    The Structure of Polymers

    There are also some polymers that,

    have a silicon or phosphorous

    backbone and these are consideredinorganic polymers.

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    Natural Polymers

    Wool, cotton, linen, hair, skin, nails,

    occurring polymers

    protein or cellulose

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    Synthetic Polymers

    Commonly referred to as plastics pliable,able to be moulded

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    The bonding process:

    they become flexible. There are no cross-

    other.

    Thermosettin ol mers do not soften

    when heated because molecules are

    crosslinked together and remain rigid.

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    Thermoplastics

    No cross links between chains.

    Weak attractive forces between chains broken

    by warming.

    Change shape - can be remoulded.

    Weak forces reform in new shape when cold.

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    Thermoplastics

    Thermoplastic polymers keep their plasticproperties

    They soften on heating and then harden

    again on cooling These polymer molecules consist of long

    chains which have only weak bonds

    e ween e c a ns

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    Thermoplastics

    The bonds between the chains are soweak that they can be broken when the

    plastic is heated

    The chains can then move around to forma erent s ape

    The weak bonds reform when it is cooled

    Thermoplastic material keeps its newshape

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    Thermosets

    Extensive cross-linking formed bycovalent bonds.

    Bonds prevent chains moving relative to

    .

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    Thermosetting

    Thermosetting polymers neversoften once they have been moulded.

    Once set into a shape, that shape

    cannot be altered These polymer molecules consist of

    long chains which have many strong

    c em ca on s e ween e c a ns

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    Thermosetting

    The bonds between the chains are so

    strong that they cannot be broken when

    This means that the thermosetting

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    Addition Polymerisation

    This bond breaks to allow the long chains

    .

    Modifying ethene, substituting different

    produces other monomers that can be

    ol merised to make ol mers with

    different properties.

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    Addition polymerisation

    Monomers contain C=C bonds

    next monomer molecule

    repeated over and over.

    Modern polymers also developed basedon alkynes R-C C - R

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    Addition Polymerisation

    A carbon = carbon double bond is neededin the monomer

    A monomer is the small molecule that

    makes up the polymer

    H H H H

    C CH H

    n

    ethene

    catalyst C CH H

    n

    ol (ethene

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    Addition Polymerisation

    The polymer is the only product Involves the o enin out of a double bond

    The conditions of the reaction can alter the

    ro erties of the ol mer Reaction proceeds by a free radical

    mechanism

    Oxygen often used as the initiator

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    Addition polymerisation

    C CH

    HH H H H

    HH H

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    Addition polymerisation

    Conditions are high pressure and an oxygeninitiator (to provide the initial free radical).

    Monomer = phenylethene

    Pol mer = ol hen lethene

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    Prediction the repeating unit

    This is easy, basically open out thedouble bond.

    H Cl H H H H

    H H H HCl Cl

    c oroe ene poly(chloroethene) akapolyvinylchloride (pvc)

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    branches

    Linear polymers are those in which themain backbone is unbranched.

    The way in which side branches are

    arranged on linear polymers(polypropylene) can affect the

    properties of the polymer.

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    branches

    Isotactic Same side of the linear ol mer

    Greater effect of dispersion forces

    therefore hi h densit , ri id and tou hand a high softening temp.

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    branches

    Atactic Irre ular oints on both sides of the

    linear polymer

    Chains of molecules cannot get closetogether, therefore low density.

    Soft, waxy little use

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    Poly(propene)

    This varying degree of randomness willaffect the strength and melting point of the

    polymer.

    The less random, the stronger the polymerand the higher the melting point

    This is because in a more ordered polymer

    ey c a ns can ge c oser oge er anhence the van der Waals forces will be

    .

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    links

    Crosslinks are covalent bonds that can formbetween polymer chains.

    If the number of crosslinks is small an

    elastomer(vulcanised rubber) will result. If the number of crosslinks is large a hard

    inflexible thermosetting polymer will be

    pro uce .

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    links To make a thermosetting polymer, the

    linear chains are produced first

    The cross linking is brought about either by

    I). heat orII). adding a chemical to react between

    the lateral functional groups linking the

    c a ns oge er. Araldite is a good example of a two part

    thermosetting polymer.

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    Condensation polymerisation uses monomersthat have two functional groups per molecule.

    These are said to be difunctional.

    Polymerisation occurs when these monomersreact head-to-tail to form a new bond that

    will eventually join the monomers together

    A small molecule (often water) is eliminated

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    Condensation Polymers

    Suitable functional groups

    -NH2 amine -OH alcohol

    O O

    -C carboxyl -C chloride

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    Condensation Pol mers

    Involves 2 monomers that have different.

    They also involve the elimination of water or

    another small molecule. Hence the term condensation polymer.

    Monomer A + Monomer B Polymer + small

    molecule (normally water).

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    Condensation Pol mers

    Common condensation polymers include

    polyamides (the amide linkage as in

    roteins . May be natural (protein, starch, cotton, wool,

    silk) or synthetic (viscose, nylon, polyester)

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    The OCR example here is terylene, a

    polymer of benzene-1,4-dicarboxylic- - , .

    HO C

    O

    C

    O

    OHn + HO CH2 CH2 OHn

    heat with

    an acid

    catalyst

    C

    O

    C

    O

    O CH2 CH2 O

    poly(ethan-1,2-diyl benzene-1,4-dicarboxylate)

    n

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    P l mi

    ese nvo ve e n age o wo monomers

    through the amide linkage as in proteinse. . silk

    This is an amide linkage:

    OC N

    H

    e am e n age

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    Nylon 6,6 a polyamide

    H H OO2 6

    H HC

    OH

    (CH2)4HO

    C

    1,6-diaminohexane hexanedioic acid

    N (CH2)6 N C

    O

    (CH2)4 C

    O

    H H

    part of a nylon polymer chain

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    Kevlar a polyamide

    CO

    CH CO

    HO OH

    OO

    N N C (CH2)4 CH H

    part of the kevlar polymer chain

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    Uses of polyamides

    The main use of polyesters and polyamides isas fibres in clothing.

    manufactured fibres woven into the natural

    material (such as cotton). This gives the material more desirable

    characteristics, such as stretchiness, andbetter washabilit .

    Dont forget that proteins are alsopolyamides, you must know how the linkage

    .

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    Addition Pol mers

    Ethene can be polymerised to produce both

    known as polyethylene)

    with high temp and high pressure long side

    chains low density (eg. plastic bags)

    Soft, flexible and translucent with a waxysurface that repels water.

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    Addition Pol mers

    High Density Polyethene (HDPE) produced with

    branches dispersion forces more effective

    . Rigid, stronger and more opaque than LDPE

    ,

    water

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    Addition Polymers

    Rubberis an addition polymer that occurs

    The monomer in natural rubber is isoprene.

    . Molecular formula (C5H8)n

    be attacked by oxygen and can perish (unlikeol thene

    Additi P l

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    Addition Pol mers

    Rubber

    not elastic long chains straighten out

    when stretched and remain this way

    uscep e o empera ure c anges

    brittle when cold and sticky when hot.

    Additi P l

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    Addition Pol mers

    Vulcanisation improved durability and

    elasticity of rubber.

    The linear chains are cross linked using

    heat and sulfur

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    Condensation Polymers

    Nylon

    Can be extruded when molten to form

    fibres or sheets of strong, durable and

    e e

    Its invention had a great impact on the

    .

    Condensation Polymers

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    Condensation Polymers

    Nylon 6 : 6

    y on s a near c a n con a n ng up o

    repeated units. e e y : e e e

    existence of 6 carbon atoms on each of the

    Condensation Polymers

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    Condensation Polymers

    PET plastic (Polyethene terephthalate).

    o r n o es

    An example of a polyester

    Note the removal of H2O (condensation

    polymer)

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    Polymer Selection

    Due to their versatility, polymers can beproduced for almost any imagined purpose.

    A huge range of polymers exist today and are

    used for many different applications. Their versatility has made them one of them

    one of the most useful classes of substances

    a we re y on n o ay s soc e y. This versatility can be attributed to the many

    eren ways a ey can e mo e

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    Recycling

    Most plastics are produced from crudeoil, coal or gas.

    and have become a visible part of our

    environmental litter.

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    Recycling