1. Polymers

2. A large molecule that is made up of many
smaller, repeating units is called a polymer
A polymer forms when hundreds or thousands of these small individual units, which are called monomers, bond together in chains.
The monomers that bond together to form a polymer may all be alike, or they may be different.
The properties of a polymer are different from those of the monomers that formed it.

3. Polymers are everywhere, making fabrics such as nylon and polyester, plastic wrap
and bottles, rubber bands, and many more products you see every day.

4. Sports activities would be different today without synthetic polymers.
Balls, uniforms, artificial turf, bandages used
to wrap sprains, and nets used in hoops and goals are usually made of synthetic polymers.

5. Living cells are efficient polymer factories.
Proteins, DNA, the chitin exoskeletons of insects, wool, silky spiderwebs and moth
cocoons, and the jellylike sacs that surround salamander eggs are polymers that are synthesized naturally.

6. The strong cellulose fibers that give tree trunks enough strength and rigidity to grow hundreds of feet tall are formed from monomers of glucose, which is a sweet crystalline solid.

7. Structure of Polymers
If you examine the structure of a polymer, you can identify the repeating monomers that formed it.
Because polymer molecules are large, they are commonly represented by showing just a piece of the chain.

8. The piece shown must include at least one complete repeating unit.
Look carefully at the structure of a segment of a cellulose molecule shown.

9. Cellulose is a polymer found in the cell walls of plant cells such as those of wood, cotton, and leaves. It is responsible for giving plants their structural strength
Notice that the ring parts of the molecule are all identical.
These are the monomer units that combine to form the polymer.
Glucose is the name of the monomer found in cellulose.

10. The complete structure of glucose is shown.

11. Another natural plant polymer that is formed from glucose monomers is starch.
Examine the structure of starch to see if you can find the difference between starch and cellulose.

12. Both cellulose and starch are made from only glucose monomers
Both cellulose and starch are made from only glucose monomers. The difference between them is the way that these monomers are bonded to each other.

13. Polymer Chemistry Classification of Polymers
The most common way of classifying polymers is to separate them into three groups - thermoplastics, thermosets, and elastomers. The thermoplastics can be divided into two types - those that are crystalline and those that are amorphous.  

15. Thermoplastics Molecules in a thermoplastic are held together by relatively weak intermolecular forces so that the material softens when exposed to heat and then returns to its original condition when cooled. Thermoplastic polymers can be repeatedly softened by heating and then solidified by cooling - a process similar to the repeated melting and cooling of metals.

16. Most linear and slightly branched polymers are thermoplastic
Most linear and slightly branched polymers are thermoplastic. All the major thermoplastics are produced by chain polymerization.
Thermoplastics have a wide range of applications because they can be formed and reformed in so many shapes. Some examples are food packaging, insulation, automobile bumpers, and credit cards.

17. Thermoplastics (80%) 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.

18. Plastics
Although the terms plastic and polymer are often used synonymously, not all polymers are plastics.
Plastics are polymers that can be molded into different shapes.
After a polymer has formed, it must be heated enough to become liquefied if it is to be poured into a mold.
After pouring, the plastic will harden if it is allowed to cool.

19. Thermoplastic materials are easy to recycle because each time they are heated, they can be poured into different molds to make new products.

20. Crystaline polymers
Highly crystalline polymers are rigid, high melting, and less affected by solvent penetration. Crystallinity makes a polymers strong, but also lowers their impact resistance. As an example, samples of polyethylene prepared under high pressure (5000 atm) have high crystallinities ( %) but are extremely brittle.

21. Crystaline polymer

22. Crystalline polymers
Areas in polymer where chains packed in regular way.
Both amorphous and crystalline areas in same polymer.
Crystalline - regular chain structure - no bulky side groups.
More crystalline polymer - stronger and less flexible.

23. Cold-drawing When a polymer is stretched a ‘neck’ forms.
What happens to the chains in the ‘neck’?
Cold drawing is used to increase a polymers’ strength.

24. Amorphous Polymers Polymer chains with branches or irregular pendant groups cannot pack together regularly enough to form crystals. These polymers are said to be amorphous

25. Amorphous regions of a polymer are made up of a randomly coiled and entangled chains. They have been compared to a bucket containing a large number of entangled worms - each one 20-feet long and of 1/4-inch thickness. The worms are so tangled that an entire worm cannot slide past the others, but small portions of the worms can twist around within the mass.

26. Amourphous polymer

27. Thermosets
A thermosetting plastic, or thermoset, solidifies or "sets" irreversibly when heated. Thermosets cannot be reshaped by heating. Thermosets usually are three-dimensional networked polymers in which there is a high degree of cross-linking between polymer chains. The cross-linking restricts the motion of the chains and leads to a rigid material

28. Thermosets are strong and durable
Thermosets are strong and durable. They primarily are used in automobiles and construction. They also are used to make toys, varnishes, boat hulls, and glues. A simulated skeletal structure of a network polymer with a high cross-link density is shown next.

29. Network Polymers Some polymers have cross-links between polymer chains creating three-dimensional networks. A high density of cross-linking restricts the motion of the chains and leads to a rigid material.A simulated skeletal structure of a network polymer with a high cross-link density is shown at the right. 

30. thermoset

31. Thermosets Extensive cross-linking formed by covalent bonds.
Bonds prevent chains moving relative to each other.
What will the properties of this type of plastic be like?

32. Longer chains make stronger polymers.
Critical length needed before strength increases.
Hydrocarbon polymers average of 100 repeating units necessary but only 40 for nylons.
Tensile strength measures the forces needed to snap a polymer.
More tangles + more touching!!!

33. Elastomers Elastomers are rubbery polymers that can be stretched easily to several times their unstretched length and which rapidly return to their original dimensions when the applied stress is released.

34. Elastomers are cross-linked, but have a low cross-link density
Elastomers are cross-linked, but have a low cross-link density. The polymer chains still have some freedom to move, but are prevented from permanently moving relative to each other by the cross-links.

35. To stretch, the polymer chains must not be part of a rigid solid - either a glass or a crystal. Rubber bands and other elastics are made of elastomers.

36. elastomer

37. Polymerization Reactions
Polymerization is a type of chemical reaction in which monomers are linked together one after another to make large chains.
The two main types of polymerization reactions are addition polymerization and condensation polymerization.
Click box to view movie clip.

38. Addition Reactions
In an addition reaction monomers that contain double bonds add onto each other, one after another, to form long chains.
The product of an addition polymerization reaction contains all of the atoms of the starting monomers.

39. Addition Reactions
The ethylene monomer contains a double bond, whereas there are none in polyethylene.

40. Addition Reactions
When monomers are added onto each other in addition polymerization, the double bonds are broken.
Thus, all of the carbons in the main chain of an addition polymer are connected by single bonds.

41. Addition polymerisation
Monomers contain C=C bonds
Double bond opens to (link) bond to next monomer molecule
Chain forms when same basic unit is repeated over and over.
Modern polymers also developed based on alkynes R-C C - R’

42. Chain-reaction polymerization, sometimes called addition polymerization, requires an initiator to start the growth of the reaction. The largest family of polymers 3, vinyl polymers, are produced by chain polymerization reactions. A good example is the free-radical polymerization of styrene, which is initiated by a free radical (R) that reacts with styrene. The compound that is formed still is a free radical, which can react again.

44. This reaction eventually leads to the formation of polystyrene

45. Polystyrene can be represented using a shorthand notation.

46. Condensation Reactions
In the second type of polymerization reactions, monomers add on one after another to form chains, as they do in an addition reaction.
However, with every new bond that is formed, a small molecule—usually water— is also formed from atoms of the monomers.
In such a reaction, each monomer must have two functional groups so it can add on at each end to another unit of the chain.

47. Condensation Reactions
This type of polymerization is called a condensation reaction because a portion of the monomer is not incorporated into the polymer but is split out—usually as water— as the monomers combine.

48. In a step-reaction polymerization reaction, sometimes called condensation polymerization, the polymer chains grow by reactions that occur between two molecular species.

50. Rubber
Another process that often occurs in combination with addition or condensation reactions is the linking together of many polymer chains. This is called cross-linking, and it gives additional strength to a polymer.

51. Rubber
In 1844, Charles Goodyear discovered that heating the latex from rubber trees with sulfur can cross-link the hydrocarbon chains in the liquid latex.
The solid rubber that is formed can be used in tires and rubber balls.

52. Copolymerisation when more than one monomer is used.
An irregular chain structure will result eg propene/ethene/propene/propene/ethene
Why might polymers designers want to design a polymer in this way?
(Hint) Intermolecular bonds!

53. What decides the properties of a polymer?
Stronger attractive forces between chains = stronger, less flexible polymer.
Chains able to slide past each other = flexible polymer .
In poly(ethene) attractive forces are weak instantaneous dipole - induced dipole, will it be flexible or not?
Nylon has strong hydrogen bonds, why does this make it a strong fibre?

54. Thermoplastics (80%) 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.

55. Plastics
Although the terms plastic and polymer are often used synonymously, not all polymers are plastics.
Plastics are polymers that can be molded into different shapes.
After a polymer has formed, it must be heated enough to become liquefied if it is to be poured into a mold.
After pouring, the plastic will harden if it is allowed to cool.

56. Plastics
Some plastics will soften and harden repeatedly as they are heated and cooled.
This property is described as being thermoplastic.
Thermoplastic materials are easy to recycle because each time they are heated, they can be poured into different molds to make new products.
Polyethylene and polyvinylchloride are examples of this type of polymer.

57. Thermosets Extensive cross-linking formed by covalent bonds.
Bonds prevent chains moving relative to each other.
What will the properties of this type of plastic be like?

58. Longer chains make stronger polymers.
Critical length needed before strength increases.
Hydrocarbon polymers average of 100 repeating units necessary but only 40 for nylons.
Tensile strength measures the forces needed to snap a polymer.
More tangles + more touching!!!

59. Crystalline polymers
Areas in polymer where chains packed in regular way.
Both amorphous and crystalline areas in same polymer.
Crystalline - regular chain structure - no bulky side groups.
More crystalline polymer - stronger and less flexible.

60. Cold-drawing When a polymer is stretched a ‘neck’ forms.
What happens to the chains in the ‘neck’?
Cold drawing is used to increase a polymers’ strength. Why then do the handles of plastic carrier bags snap if you fill them full of tins of beans?

61. Question 1
Identify the repeating unit that appears in each of the following polymers.
I think this should read “Identify the repeating unit that appears in the following polymer.” The question originally had multiple parts, but we are only using one.

62. Answer

63. Question 2
Draw the structure of the polymer that will be formed from the monomer shown.
Again, we only used one part, so I think this should read, “Draw the structure of the polymer that will be formed from the monomer shown.”

64. Answer

65. nylon
Called a copolymer= formed from the combination of 2 different polymers
Hexamethylenediamine
Adipic acid
See page 1020

66. Natural Polymers