Representative polymers
Bakelite
The first plastic based on a synthetic polymer was made from phenol and
formaldehyde, with the first viable and cheap synthesis methods invented in
1907, by Leo Hendrik Baekeland, a Belgian-born American living in New York
state. Baekeland was looking for an insulating shellac to coat wires in
electric motors and generators. He found that combining phenol (C6H5OH) and
formaldehyde (HCOH) formed a sticky mass and later found that the material
could be mixed with wood flour, asbestos, or slate dust to create strong and
fire resistant "composite" materials. The new material tended to foam
during synthesis, requiring that Baekeland build pressure vessels to force out
the bubbles and provide a smooth, uniform product, as he announced in 1909, in
a meeting of the American Chemical Society. Bakelite was originally used for
electrical and mechanical parts, coming into widespread use in consumer goods
and jewelry in the 1920s. Bakelite was a purely synthetic material, not derived
from living matter. It was also an early thermosetting plastic.
Polystyrene
Unplasticised polystyrene is a rigid, brittle, inexpensive plastic that
has been used to make plastic modelkits and similar knick-knacks. It also is
the basis for some of the most popular "foamed" plastics, under the
name styrene foam or Styrofoam. Like most other foam plastics, foamed
polystyrene can be manufactured in an "open cell" form, in which the
foam bubbles are interconnected, as in an absorbent sponge, and "closed
cell", in which all the bubbles are distinct, like tiny balloons, as in
gas-filled foam insulation and flotation devices. In the late 1950s, high
impact styrene was introduced, which was not brittle. It finds much current use
as the substance of toy figurines and novelties.
Polyvinyl chloride
Polyvinyl chloride (PVC, commonly called "vinyl")
incorporates chlorine atoms. The C-Cl bonds in the backbone are hydrophobic and
resist oxidation (and burning). PVC is stiff, strong, heat and weather
resistant, properties that recommend its use in devices for plumbing, gutters,
house siding, enclosures for computers and other electronics gear. PVC can also
be softened with chemical processing, and in this form it is now used for
shrink-wrap, food packaging, and rain gear.
All PVC polymers are degraded by heat and light. When this happens,
hydrogen chloride is released into the atmosphere and oxidation of the compound
occurs. Because hydrogen chloride readily combines with water vapor in the air
to form hydrochloric acid, polyvinyl chloride is not recommended for long-term
archival storage of silver, photographic film or paper (mylar is preferable).
Nylon
The plastics industry was revolutionized in the 1930s with the
announcement of polyamide (PA), far better known by its trade name nylon. Nylon
was the first purely synthetic fiber, introduced by DuPont Corporation at the
1939 World's Fair in New York City.
In 1927, DuPont had begun a secret development project designated
Fiber66, under the direction of Harvard chemist Wallace Carothers and chemistry
department directorElmer Keiser Bolton. Carothers had been hired to perform
pure research, and he worked to understand the new materials' molecular
structure and physical properties. He took some of the first steps in the molecular
design of the materials.
His work led to the discovery of synthetic nylon fiber, which was very
strong but also very flexible. The first application was for bristles for
toothbrushes. However, Du Pont's real target was silk, particularly silk
stockings. Carothers and his team synthesized a number of different polyamides
including polyamide 6.6 and 4.6, as well as polyesters.
It took DuPont twelve years and US$27 million to refine nylon, and to
synthesize and develop the industrial processes for bulk manufacture. With such
a major investment, it was no surprise that Du Pont spared little expense to
promote nylon after its introduction, creating a public sensation, or
"nylon mania".
Nylon mania came to an abrupt stop at the end of 1941 when the USA
entered World War II. The production capacity that had been built up to produce
nylon stockings, or just nylons, for American women was taken over to
manufacture vast numbers of parachutes for fliers and paratroopers. After the
war ended, DuPont went back to selling nylon to the public, engaging in another
promotional campaign in 1946 that resulted in an even bigger craze, triggering
the so-called nylon riots.
Subsequently polyamides 6, 10, 11, and 12 have been developed based on
monomers which are ring compounds; e.g. caprolactam. Nylon 66 is a material
manufactured bycondensation polymerization.
Nylons still remain important plastics, and not just for use in
fabrics. In its bulk form it is very wear resistant, particularly if
oil-impregnated, and so is used to build gears, plain bearings, valve seats,
seals and because of good heat-resistance, increasingly for under-the-hood
applications in cars, and other mechanical parts.
Poly(methyl methacrylate)
Poly(methyl methacrylate) (PMMA), also known as acrylic or acrylic
glass as well as by the trade names Plexiglas, Acrylite, Lucite, and Perspex
among several others (see below), is a transparent thermoplastic often used in
sheet form as a lightweight or shatter-resistant alternative to glass. The same
material can be utilised as a casting resin, in inks and coatings, and has many
other uses.
Rubber
Natural rubber is an elastomer (an elastic hydrocarbon polymer) that
originally was derived from latex, a milky colloidal suspension found in
specialised vessels in some plants. It is useful directly in this form (indeed,
the first appearance of rubber in Europe was cloth waterproofed with
unvulcanized latex from Brazil). However, in 1839, Charles Goodyearinvented
vulcanized rubber; a form of natural rubber heated with sulfur (and a few other
chemicals), forming cross-links between polymer chains (vulcanization),
improving elasticity and durability.
In 1851, Nelson Goodyear added fillers to natural rubber materials to
form ebonite.
Synthetic rubber
The first fully synthetic rubber was synthesized by Sergei Lebedev in
1910. In World War II, supply blockades of natural rubber from South East Asia
caused a boom in development of synthetic rubber, notably styrene-butadiene
rubber. In 1941, annual production of synthetic rubber in the U.S. was only 231
tonnes which increased to 840,000 tonnes in 1945. In the space race and nuclear
arms race, Caltech researchers experimented with using synthetic rubbers for
solid fuel for rockets. Ultimately, all large military rockets and missiles
would use synthetic rubber based solid fuels, and they would also play a
significant part in the civilian space effort.