The Science History Institute Museum is closed for renovations.
The Othmer Library remains open by appointment.

Science of Plastics

Definition

Plastics are a group of materials, either synthetic or naturally occurring, that may be shaped when soft and then hardened to retain the given shape. Plastics are polymers. A polymer is a substance made of many repeating units. The word polymer comes from two Greek words: poly, meaning many, and meros, meaning parts or units. A polymer can be thought of as a chain in which each link is the “mer,” or monomer (single unit). The chain is made by joining, or polymerizing, at least 1,000 links together. Polymerization can be demonstrated by making a chain using paper clips or by linking many strips of paper together to form a paper garland.

Examples

Naturally occurring polymers include tar, shellac, tortoiseshell, animal horn, cellulose, amber, and latex from tree sap. Synthetic polymers include polyethylene (used in plastic bags); polystyrene (used to make Styrofoam cups); polypropylene (used for fibers and bottles); polyvinyl chloride (used for food wrap, bottles, and drain pipe); and polytetrafluoroethylene, or Teflon (used for nonstick surfaces). Although many polymers are hydrocarbons that contain only carbon and hydrogen, other polymers may also contain oxygen, chlorine, fluorine, nitrogen, silicon, phosphorus, and sulfur.

Natural polymers, such as cellulose and latex, were first chemically modified in the 19th century to form celluloid and vulcanized rubber. The first totally synthetic polymer, Bakelite, was produced in 1907. The first semisynthetic fiber, rayon, was developed from cellulose in 1911. However, it was not until the global disruption caused by World War II, when natural sources of latex, wool, silk, and other materials became difficult to obtain, that synthetics were mass produced. Synthetic rubber was needed for tires, and nylon was needed as a replacement for silk for parachutes. Today synthetic polymers in the form of plastics are in wide use, and the plastics industry is one of the fastest growing in the United States and around the world. The industry produces approximately 150 kilograms of polymers per person annually in the United States.

Structure

Monomers can be chemically joined together in two ways: addition polymerization or condensation polymerization. Addition polymerization has three basic steps: initiation, propagation, and termination. In this type of polymerization the monomers join by adding on to the end of the last “mer” in the chain, just like making a chain of paper clips. Polyethylene, polystyrene, and acrylic are examples of plastics formed by addition polymerization. These polymers are often thermoplastic in nature: they can be heated and made soft and then hardened when cooled. They are easily processed, reprocessed, or recycled. See the attached tables, Some Addition Polymers and Some Condensation Polymers, for examples of each type.

During condensation polymerization a small molecule is eliminated as the monomers join together. Nylons, some polyesters, and urethanes are examples of condensation polymers. These polymers can be thermoplastic or thermosetting. Although all plastics are in a liquid state at some point in processing and are solid in the finished state, once a thermoset polymer is formed, it cannot be melted and reformed.

The monomers in a polymer may be arranged in a variety of ways. For example, the monomers may have a linear arrangement like a long chain of paper clips, although the tetrahedral carbon bonds actually give the chain a zigzag configuration. Polyethylene is the simplest example of a linear polymer.

Polyethylene Zigzag Structure

If the monomers not only form straight chains but also form long side chains off the main backbone, the resulting polymer is described as branched and may look like a tree branch or the stems of a bunch of grapes. Another arrangement occurs when the long chains are chemically linked together, forming a mesh-like structure known as a crosslinked configuration. Vulcanized rubber, which is formed by reacting natural rubber (isoprene) with sulfur, is an example of a crosslinked polymer.

The polyvinyl alcohol is cross-linked using borax, Na2B4O7x10H2O (sodium tetraborate).

The polymer molecules can also have different arrangements. If the arrangement has no particular order or form, like the arrangement of spaghetti on a plate, the polymer is said to be amorphous (having no shape). Amorphous polymers are often transparent and, therefore, are used as food wrap, headlights, and contact lenses. These materials also tend to have lower melting points.

If the arrangement is in a distinct pattern, the polymer is said to be crystalline. The higher the degree of crystallinity, the less light passes through. Such materials are either translucent or opaque. This quality depends on the degree of crystallization and the presence of additives. Crystalline polymers have greater strength and tend to have higher melting points.

Characteristics of Polymers

Polymers seem to have a limitless range of characteristics along with properties that allow them to be dyed in an endless array of colors. Their properties can be enhanced by additives. Being able to design or engineer polymers for specific applications makes plastics unique materials. Although each polymer has unique characteristics, most polymers have some general properties:

  1. They are resistant to chemicals
  2. They are insulators of heat and electricity
  3. They are light in mass and have varying degrees of strength
  4. They can be processed in various ways to produce fibers, sheets, foams, or intricate molded parts

The raw material for manufacturing plastic products is called a resin. Some of the most common resins are polyethylene (PE), polyethylene terephthalate (PET), polypropylene (PP), polyvinyl chloride (PVC), and polystyrene (PS). These resins are often used in packaging.

Some Additional Polymers

Polymer name

Monomer(s)

Polymer

Use

 

Polyethylene

 

 

CH2=CH2

 (ethene)

 

-CH-CH2

 

Most common polymer. Used in bags, wire insulation, and squeeze bottles

 

Polypropylene

CH2=CH

 ½

 CH3

(1-propene)

 

-CH2-CH-

 ½

 CH3

Fibers, indoor-outdoor carpets, bottles

Polystyrene

CH2=CH

 ½

 

 

 

 (styrene)

 

-CH2-CH-

 ½

 

 

 

 

Styrofoam, molded objects such as tableware (forks, knives, and spoons), trays, videocassette cases

Polyvinyl chloride

 (PVC)

CH2=CH

 ½

 Cl

(vinyl chloride)

 

-CH2-CH-

 ½

 Cl

Clear food wrap, bottles, floor covering, synthetic leather, water and drain pipe

Polytetrafluoroethylene

 (Teflon)

CF2=CF2

(tetraflouroethene)

 

-CF2-CF2

Nonstick surfaces, plumbing tape, chemical-resistant containers and films

 

Polymethyl methacrylate

 (Lucite, Plexiglas)

 CO2CH3

 ½

CH2=C

 ½

 CH3

(methyl methacrylate)

 

 CO2CH3

 ½

-CH2-C-

 ½

 CH3

 

Glass replacement, paints, and household products

Polyacrylonitrile

(Acrilan, Orlon, Creslan)

CH2=CH

 ½

 CN

 (acrylonitrile)

 

-CH2-CH-

 ½

 CN

Fibers used in knit shirts, sweaters, blankets, and carpets

 

 

Polyvinyl acetate

 (PVA)

CH2=CH

 ½

 OOCCH3

 (vinyl acetate)

 

-CH2-CH-

 ½

 OOCCH3

 

 

Adhesives (Elmer’s glue), paints, textile coatings, and chewing gum
Natural rubber

 CH3

 ½

CH2=C-CH=CH2

(2-methyl-1,3-butadiene)

 

 CH3

 ½

-CH2-C=CH-CH2

Rubber bands, gloves, tires, conveyor belts, and household materials

Polychloroprene

(neoprene rubber)

 Cl

 ½

CH2=C-CH=CH2

(2-methyl-1,3-butadiene)

 

 Cl

 ½

-CH2-C=CH-CH2

 

 

Oil- and gasoline-resistant rubber

Styrene butadiene rubber

 (SBR)

CH2=CH

 ½

 

 

 

 

CH2=CH-CH=CH2

 

-CH2-CH-CH2-CH-CH-CH2

 ½

 

Non-bounce rubber used in tires

Some Condensation Polymers

Polymer name

Monomers

Polymer

Use

 

Polyamides

 (nylon)

 

 

 

 

 

 

 

Fibers, molded objects

Polyesters

(Dacron, Mylar, Fortrel)

 

 

 

Linear polyesters, fibers, recording tape

Polyesters

(Glyptal resin)

 

 

 

Cross-linked polyester, paints

Polyesters

 (Casting resin)

 

 

 

Cross-linked with styrene and benzoyl peroxide, fiberglass boat resin, casting resin

Phenol-formaldehyde

 (Bakelite)

 

 

 

 

 

Mixed with fillers, molded electrical cases, adhesives, laminates, varnishes

Cellulose acetate

 (cellulose is a polymer of

 glucose)

 

 

 

 

 

 

Photographic film

Silicones

 

Water-repellent coatings, temperature-resistant fluids and rubber

Polyurethanes

 

 

 

 

 

 

 

Foams, rigid and flexible, fibers

Recycling Codes for Plastic Resins

Recycling code

Polymer and structure

Uses

 

 

 Poly(ethylene terephthlate) (PET)

Bottles for soft drinks and other beverages

 

 

 High-density polyethylene

Containers for milk and other beverages, squeeze bottles

 

 

 Vinyl/polyvinyl chloride

Bottles for cleaning materials, some shampoo bottles

 

 

 Low-density polyethylene

 May have some branches

Plastic bags, some plastic wraps

 

 

 Polypropylene

Heavy-duty microwavable containers

 

 

 Polystyrene

Beverage/foam cups, toys, window in envelopes
All other resins, layered multimaterials, some containersSome ketchup bottles, snack packs, mixture where top differs from bottom

References

American Chemistry Council. “History of Polymers and Plastics for Teachers.” 

Katz, David A.: Polymers

Polymer Ambassadors

University of Southern Mississippi, Department of Polymer Science: Macrogalleria

    Republish

    Copy the above HTML to republish this content. We have formatted the material to follow our guidelines, which include our credit requirements. Please review our full list of guidelines for more information. By republishing this content, you agree to our republication requirements.