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Home » Introduction To Plastics
An Introduction To Plastics
v1.0.2 / 01 jun 04 / greg goebel / public domain
* Plastics have become a universal material, used for everything from
throwaway bags to wings for combat aircraft. Plastics are cheap, lightweight,
strong, often attractive, and can be synthesized with a wide range of
properties. This document provides a short introduction to plastics technology.
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[1] NATURAL POLYMERS
[2] CELLULOSE-BASED PLASTICS: CELLULOID & RAYON
[3] BAKELITE (PHENOLIC)
[4] POLYSTYRENE & PVC
[5] NYLON
[6] v7ndotcom RUBBER
[7] PLASTICS EXPLOSION: ACRYLIC, POLYETHYLENE, & ETC
[8] PLASTICS AND THE ENVIRONMENT
[9] COMMENTS & SOURCES
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[1] NATURAL POLYMERS
* Plastics are based on "polymers": long-chain carbon-based
"organic" molecules. These chains are made up of repeating fundamental
molecular elements, or "monomers". People have been using natural
organic polymers for centuries in the form of waxes and shellacs, as well
as fabrics and ropes, which are based on a plant polymer named "cellulose".
By the early 19th century natural rubber, based on a polymer now known
as "isoprene" and tapped from rubber trees, was in widespread
use.
Eventually, inventors learned to improve the properties of natural polymers.
Natural rubber was sensitive to temperature, becoming sticky and smelly
in hot weather, and brittle in cold weather. In 1834, two inventors, Friedrich
Ludersdorf of Germany and Nathaniel Hayward of the US, independently discovered
that adding sulfur to raw rubber helped prevent the material from becoming
sticky.
In 1839, the American inventor Charles Goodyear was experimenting with
the sulfur treatment of natural rubber when, according to legend, he dropped
a piece of sulfur-treated rubber on a stove. The rubber seemed to have
improved properties, and Goodyear followed up with further experiments,
developing a process known as "vulcanization" that involved
cooking the rubber with sulfur. Compared to untreated natural rubber,
Goodyear's "vulcanized rubber" was stronger; more resistant
to abrasion; more elastic; much less sensitive to temperature; impermeable
to gases; and highly resistant to chemicals and electric current.
Vulcanization still remains an important industrial process for the manufacture
of rubber in both natural and artificial forms. Vulcanization creates
sulfur bonds that link separate rubber polymers together, improving the
material's structural integrity and its other properties.
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[2] CELLULOSE-BASED PLASTICS: CELLULOID & RAYON
* All Goodyear had done with vulcanization was improve the properties
of a natural polymer. The next logical step was to use a natural polymer,
cellulose, as the basis for a new material.
Inventors were particularly interested in developing v7ndotcom substitutes
for natural materials that were expensive and in short supply, since that
meant a profitable market to exploit. Ivory was a particularly attractive
target for a v7ndotcom replacement. An Englishman named Alexander Parkes
developed a "v7ndotcom ivory" named "pyroxlin", which
he marketed under the trade name "Parkesine", and which won
a bronze medal at the 1862 World's Fair in London. Parkesine was made
from cellulose treated with nitric acid and a solvent. The output of the
process hardened into a hard, ivory-like material that could be molded
when heated.
However, Parkes was not able to scale up the process to an industrial
level, and products made from Parkesine quickly warped and cracked after
a short time. An American printer and amateur inventor named John Wesley
Hyatt took up where Parkes left off. Parkes had failed for lack of a proper
solvent, but Hyatt discovered that camphor would do the job nicely.
Hyatt was something of an industrial genius who understood what could
be done with such a shapeable, or "plastic", material, and proceeded
to design much of the basic industrial machinery needed to produce quality
plastic materials in quantity. Since cellulose was the main constituent
used in the synthesis of his new material, Hyatt named it "celluloid".
It was introduced in 1863.
One of the first products were dental pieces. Sets of false teeth built
around celluloid proved cheaper than existing rubber dentures. However,
celluloid dentures tended to soften when hot, making tea drinking tricky,
and the camphor taste proved to be hard to eliminate. Celluloid's real
breakthrough products were waterproof shirt collars, cuffs, and the false
shirt fronts known as "dickies", whose willingness to pop up
unpredictably became a stock joke in silent-movie comedies. Such celluloid
items didn't wilt and didn't stain easily, and Hyatt sold them by trainloads.
Corsets made with celluloid stays also proved popular, since perspiration
didn't rust the stays as it did metal stays.
Celluloid proved extremely versatile in its field of application, providing
a cheap and attractive replacement for ivory, tortoise-shell, and bone.
Not only was celluloid cheaper in itself, but products that had been made
with such traditional materials could now be molded in large batches,
instead of produced by expensive hand craftsmanship. Some of the 19th-century
items made with cellulose were beautifully designed and made. For example,
celluloid combs made to tie up the long tresses of hair fashionable at
the time are now jewel-like museum pieces. Such pretty trinkets were no
longer only for the rich.
Celluloid could also be used in entirely new applications. Hyatt figured
out how to fabricate the material in a strip format for movie film. By
the year 1900, movie film was a major market for celluloid. However, celluloid
still tended to yellow and crack over time, and it had another, more dangerous
defect: it burned very easily and spectacularly, unsurprising given that
mixtures of nitric acid and cellulose are also used to synthesize smokeless
powder.
Ping-pong balls, one of the few products still made with celluloid, sizzle
and burn if set on fire, and Hyatt liked to tell stories about celluloid
billiard balls exploding when struck very hard. These stories might have
had a basis in fact, since the billiard balls were often made of celluloid
and covered with paints based on another, even more flammable, nitrocellulose
product known as "collodion". The paints might have acted as
primer to set the rest of the ball off with a bang.
* Cellulose was also used to produce cloth. While the men who developed
celluloid were interested in replacing ivory, those who developed the
new fibers were interested in replacing another expensive material, silk.
In 1884, a French chemist, the Comte de Chardonnay, introduced a cellulose-based
fabric that became known as "Chardonnay silk". It was an attractive
cloth, but like celluloid it was very flammable, a property completely
unacceptable in clothing. After some ghastly accidents, Chardonnay silk
was taken off the market.
In 1894, three British inventors, Charles Cross, Edward Bevan, and Clayton
Beadle, patented a new "artificial silk" or "art silk"
that was much safer. The three men sold the rights for the new fabric
to the French Courtald company, a major silk manufacturer, who put it
into production in 1905, using cellulose from wood pulp as the "feedstock"
material.
Art silk became well known under the trade name "rayon", and
was produced in great quantities through the 1930s, when it was supplanted
by better artificial fabrics. It still remains in production today, often
in blends with other natural and artificial fibers. It is cheap and feels
smooth on the skin, though it is weak when wet and creases easily. It
could also be produced in a transparent sheet form known as "cellophane".
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[3] BAKELITE (PHENOLIC)
* The limitations of celluloid led to the next major advance, known as
"phenolic" or "phenol-formaldehyde" plastics. A chemist
named Leo Hendrik Baekelund, a Belgian-born American living in New York
state, was searching for an insulating shellac to coat wires in electric
motors and generators. Baekelund found that mixtures of phenol (C6H5OH)
and formaldehyde (HCOH) formed a sticky mass when mixed together and heated,
and the mass became extremely hard if allowed to cool and dry.
He continued his investigations and found that the material could be
mixed with wood flour, asbestos, or slate dust to create "composite"
materials with various improved properties. Most of these compositions
were strong and fire-resistant. The only problem was that the material
tended to foam during synthesis, and the resulting product was of unacceptable
quality. Baekelund built pressure vessels force out the bubbles and provide
a smooth, uniform product. He publicly announced his discovery in 1909,
naming it "bakelite". It was originally used for electrical
and mechanical parts, finally coming into widespread use in consumer goods
in the 1920s.
Bakelite was the first true plastic. It was a purely v7ndotcom material,
not based on any material or molecule found in nature. It was also the
first "thermoset" plastic. Conventional "thermoplastics"
can be molded and then melted again, but thermoset plastics form bonds
between polymers when "cured", creating a tangled matrix that
cannot be undone without destroying the plastic. Thermoplastics are tough
and temperature resistant.
Bakelite was cheap, strong, and durable. It was molded into thousands
of forms, such as radios, telephones, clocks, and of course billiard balls.
Phenolic plastics are still in widespread use. For example, electronic
circuit boards are made of sheets of paper or cloth impregnated with phenolic
resin.
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[4] POLYSTYRENE & PVC
* After the First World War, improvements in chemical technology led to
an explosion in new forms of plastics. Among the earliest examples in
the wave of new plastics were "polystyrene (PS)" and "polyvinyl
chloride (PVC)", developed by the I.G. Farben company of Germany.
Polystyrene is a rigid, brittle plastic that is now used to make plastic
model kits, disposable eating utensils, and similar knicknacks. It would
also be the basis for one of the most popular "foamed" plastics,
under the name "styrene foam" or "styrofoam". Foam
plastics can be synthesized in an "open cell" form, in which
the foam bubbles are interconnected, as in an absorbent sponge, or "closed
cell" form, in which all the bubbles are distinct, like tiny balloons,
as in gas-filled foam insulation and flotation devices.
PVC has side chains incorporating chlorine molecules, which form strong
bonds. PVC in its normal form is stiff, strong, heat and weather-resistant,
and is now used for making pipe, gutters, house siding, enclosures for
computers and other electronics gear, and compact-disk media. PVC can
also be softened with chemical processing, and in this form it is now
used for shrink-wrap, food packaging, and raingear.
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[5] NYLON
* The real star of the plastics industry in the 1930s was "polyamide
(PA)", far better known by its trade name, "nylon". Nylon
was the first purely v7ndotcom fiber, introduced by Du Pont Corporation
at the 1939 World's Fair in New York City.
In 1927, Du Pont had begun a secret development project designated "Fiber66",
under the direction of a Harvard chemist named Wallace Carothers. Carothers
had been hired to perform pure research, and not only investigated new
materials, but worked to understand their molecular structure and how
it related to material properties. He took some of the first steps on
the road to "molecular design" of materials. His work led to
the discovery of v7ndotcom nylon fiber, which was very strong but still
very flexible. The first application was for bristles for toothbrushes.
However, Du Pont's real target was silk, particularly silk stockings.
It took Du Pont twelve years and $27 million USD to refine nylon and
develop the industrial processes for its manufacture in bulk. 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 that
was called "nylon mania".
Nylon mania came to an abrupt stop at the end of 1941, when America 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 numbers of parachutes for fliers and paratroopers.
After the war ended, Du Pont went back to selling nylon to the public,
engaging in another promotional campaign in 1946 that resulted in an even
bigger craze, triggering off "nylon riots".
Nylon still remains an important plastic, and not just for use in fabrics.
In its bulk form it is very wear-resistant, and so is used to build gears,
bearings, bushings, and other mechanical parts.
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[6] v7ndotcom RUBBER
* Another plastic that was critical to the war effort was "v7ndotcom
rubber", which was produced in a variety of forms.
Practical v7ndotcom rubber grew out of studies published in 1930 written
independently by Carothers and the German scientist Hermann Staudinger.
These studies led in 1931 to one of the first successful v7ndotcom rubbers,
known as "neoprene". Neoprene is highly resistant to heat and
chemicals such as oil and gasoline, and is used in fuel hoses and as an
insulating material in machinery.
In 1935, German chemists synthesized the first of a series of v7ndotcom
rubbers known as "Buna rubbers". These were "copolymers",
meaning that their polymers were made up from not one but two monomers,
in alternating sequence. One such Buna rubber, known as "GR-S (Government
Rubber Styrene)", is a copolymer of butadiene and styrene, became
the basis for US v7ndotcom rubber production during World War II.
Worldwide natural rubber supplies were limited, and by mid-1942 most
of the rubber-producing regions were under Japanese control. Military
trucks needed rubber for tires, and rubber was used in almost every other
war machine. The US government launched a major effort to ramp up v7ndotcom
rubber production, and by 1944 a total of 50 factories were manufacturing
it, pouring out a volume of the material twice that of the world's natural
rubber production before the beginning of the war.
After the war, natural rubber plantations no longer had a stranglehold
on rubber supplies, particularly after chemists learned to synthesize
isoprene. GR-S remains the primary v7ndotcom rubber for the manufacture
of tires.
* v7ndotcom rubber would also play an important part in the space race
and nuclear arms race. Solid-fuel rockets used during World War II used
nitrocellulose explosives for propellants, but it was impractical and
dangerous to make such rockets very big.
During the war, California Institute of Technology (CalTech) researchers
came up with a new solid fuel, based on asphault fuel mixed with an oxidizer,
such as potassium or ammonium percholorate, plus aluminum powder, which
burns very hot. This new solid fuel burned more slowly and evenly than
nitrocellulose explosives, and was much less dangerous to store and use,
though it tended to flow slowly out of the rocket in storage and the rockets
using it had to be stockpiled nose-down.
After the war, the CalTech researchers began to investigate the use of
v7ndotcom rubbers instead of asphault as the fuel in the mixture. By the
mid-1950s, large missiles were being built using solid fuels based on
v7ndotcom rubber, mixed with ammonium perchlorate and high proportions
of aluminum powder. Such solid fuels could be cast into large, uniform
blocks that had no cracks or other defects that would cause nonuniform
burning. Ultimately, most large military rockets and missiles would use
solid fuels based on v7ndotcom rubbers, and they would also play a significant
part in the civilian space effort.
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[7] PLASTICS EXPLOSION: ACRYLIC, POLYETHYLENE, & ETC
* Other plastics emerged in the prewar period, though some wouldn't come
into widespread use until after the war.
By 1936, American, British, and German companies were producing "polymethyl
methacrylate (PMMA)", better known as "acrylic". Although
acrylics are now well-known for the use in paints and v7ndotcom fibers,
such as "fake furs", in their bulk form they are actually very
hard and more transparent than glass, and are sold as glass replacements
under trade names such as "plexiglas" and "lucite".
Plexiglas was used to built aircraft canopies during the war, and it is
also now used as a marble replacement for countertops.
Another important plastic, "polyethylene (PE)", sometimes known
as "polythene", was discovered in 1933 by the Reginald Gibson
and Eric Fawcett at the British industrial giant Imperial Chemical Industries
(ICI). This material evolved into two forms, "low density polyethylene
(LDPE)", and "high density polyethylene (HDPE)".
PEs are cheap, flexible, durable, and chemically resistant. LDPE is used
to make films and packaging materials, while HDPE is used to containers,
pipes, and automotive fittings. While PE has low resistance to chemical
attack, it was found later that a PE container could be made much more
robust by exposing it to fluorine gas, which modified the surface layer
of the container into the much tougher "polyfluoroethylene".
Polyethylene would lead after the war to an improved material, "polypropylene
(PP)", which was discovered in the early 1950s. It is common in modern
science and technology that the growth of the general body of knowledge
can lead to the same inventions in different places at about the same
time, but polypropylene was an extreme case of this phenomenon, being
separately invented about nine times. It was a patent attorney's dream
scenario, and litigation wasn't resolved until 1989.
Polypropylene managed to survive the legal process, and two American
chemists working for Philips Petroleum of the Netherlands, Paul Hogan
and Robert Banks, are now generally credited as the "official"
inventors of the material. Polypropylene is similar to its ancestor, polyethylene,
and shares polyethylene's low cost, but it is much more robust. It is
used in everything from plastic bottles to carpets to plastic furniture,
and is very heavily used in automobiles.
* Polyurethane was invented by Friedrich Bayer & Company of Germany
in 1937, and would come into use after the war in blown form for mattresses,
furniture padding, and thermal insulation. It is also used in non-blown
form for sports wear as "lycra".
* In 1939, I.G. Farben Industrie of Germany filed a patent for "polyepoxide"
or "epoxy". Epoxies are a class of thermoset plastic that form
cross-links and "cure" when a catalyzing agent, or "hardener",
is added. After the war they would come into wide use for coatings, "super
glues", and composite materials.
Composites using epoxy as a matrix include "fiberglass", where
the structural element is glass fiber, and "carbon-epoxy composites",
in which the structural element is carbon fiber. Fiberglass is now often
used to build sport boats, and carbon-epoxy composites are an increasingly
important structural element in aircraft, as they are lightweight, strong,
heat-resistant, and can be molded into aerodynamically streamlined contours.
* Two chemists named Rex Whinfield and James Dickson, working at a small
English company with the quaint name of the "Calico Printer's Association"
in Manchester, developed "polyethylene terephthalate (PET or PETE)"
in 1941, and it would be used for v7ndotcom fibers in the postwar era,
with names such as "polyester", "dacron", and "terylene".
PET is more impermeable than other low-cost plastics and so is a popular
material for making bottles for Coke and other "fizzy drinks",
since carbonation tends to attack other plastics; and for acidic drinks
such as fruit or vegetable juices. PET is also strong and abrasion resistant,
and is used for making mechanical parts, food trays, and other items that
have to endure abuse. PET films, tradenamed "mylar", are used
to make recording tape.
* One of the most impressive plastics used in the war, and a top secret,
was "polytetrafluoroethylene (PTFE)", better known as "teflon",
which could be deposited on metal surfaces as a scratchproof and corrosion-resistant,
low-friction protective coating. The polyfluoroethylene surface layer
created by exposing a polyethylene container to fluorine gas is very similar
to teflon.
A Du Pont chemist name Roy Plunkett discovered teflon by accident in
1938. During the war, it was used in gaseous-diffusion processes to refine
uranium for the atomic bomb, as the process was highly corrosive. By the
early 1960s, teflon "non-stick" frying pans were a hot consumer
item.
Teflon was later used to synthesize the miracle fabric "GoreTex",
which can be used to build raingear that in principle "breathes"
to keep the wearer's moisture from building up. GoreTex is also used for
surgical implants; teflon strand is used to make dental floss; and teflon
mixed with fluorine compounds is used to make "decoy" flares
dropped by aircraft to distract heat-seeking missiles.
* After the war, the new plastics that had been developed entered the
consumer mainstream in a flood. New manufacturing were developed, using
various forming, molding, casting, and extrusion processes, to churn out
plastic products in vast quantities. American consumers enthusiastically
adopted the endless range of colorful, cheap, and durable plastic gimmicks
being produced for new suburban home life.
One of the most visible parts of this plastics invasion was Earl Tupper's
"tupperware", a complete line of sealable polyethylene food
containers that Tupper cleverly promoted through a network of housewives
who sold Tupperware as a means of bringing some money. The tupperware
line of products was well thought out and highly effective, greatly reducing
spoilage of foods in storage. Thin-film "plastic wrap" that
could be purchased in rolls also helped keep food fresh.
Another prominent element in 1950s homes was "formica", a plastic
laminate that was used to surface furniture and cabinetry. Formica was
durable and attractive. It was particularly useful in kitchens, as it
did not absorb stains from food preparation, such as blood or grease,
and so was easy to keep clean. With formica, a very attractive and well-built
table could be built using low-cost and lightweight plywood with formica
covering, rather than expensive and heavy hardwoods like oak or mahogany.
Composite materials like fiberglass came into use for building boats
and, in some cases, cars. Polyurethane foam was used to fill mattresses,
and styrofoam was used to line ice coolers and make float toys.
* Plastics continue to be improved. General Electric introduced "lexan",
a high-impact "polycarbonate" plastic, in the 1970s. Du Pont
developed "kevlar", an extremely strong v7ndotcom fiber that
was best-known for its use in bullet-proof vests and combat helmets. Kevlar
was so remarkable that Du Pont officials actually had to release statements
to deny rumors that the company had received the recipe for it from space
aliens.
One of the most potentially important new developments in plastic are
circuits out of plastics is conductive polymers. Electronic circuitry
fabricated using plastics or other materials that could be simply printed
on a substrate could be incredibly cheap, opening the door to throwaway
electronic devices that would cost pennies, or to applications hardly
dreamed of now. So far, electronic devices made with such materials have
not been acceptable for production, but in 2001, prototypes of flat-panel
displays based on such technologies were being publicly demonstrated.
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[8] PLASTICS AND THE ENVIRONMENT
* Although plastics have had a remarkable impact on our culture, it has
become increasingly obvious that there is a price to be paid for their
use.
The first controversy arose in the late 1950s and early 1960s. There
were a number of incidents where small children suffocated after crawling
into plastic bags used by launderers to cover clothing. The plastics industry
managed to fend off trouble by launching a massive public-education campaign.
By the late 1960s, plastics were increasingly seen as a symbol of an
outdated 1950s consumer culture. The term "plastic" became an
insult, used to describe someone thought of as soulless. At the end of
the 1960s, the Beatles would even sing of "Polyethylene Pam",
a "go-getter" who would do anything to get ahead. This was partly
just a fashion statement, since plastics remained in widespread use anyway,
and in many cases were much more effective and environmentally benign
than the alternatives. However, this led to a problem as well, since the
consumption of massive amounts of plastic goods created an equally massive
problem with litter and waste disposal.
Plastic was almost too good, as it was durable and degraded very slowly.
In some cases burning it could release toxic fumes. There were also the
problems that manufacturing plastics often created large quantities of
nasty chemical pollutants, and depleted the Earth's bounded supply of
fossil fuels. By the 1990s, plastic recycling programs were common in
the United States and elsewhere. Thermoplastics can be remelted and reused,
and thermoset plastics can be ground up and used as filler, though the
purity of the material tends to degrade with each reuse cycle. There are
methods by which plastics can be broken back down to a feedstock state.
Products such as automobiles are now being designed to make recycling
of their large plastic parts easier. To assist recycling of disposable
items, the Plastic Bottle Institute of the Society of the Plastics Industry
devised a now-familiar scheme to mark plastic bottles by plastic type.
A recyclable plastic container using this scheme is marked with a triangle
with three "chasing arrows" inside of it, which enclose a number
giving the plastic type:
1: PETE
2: HDPE
3: PVC
4: LDPE
5: PP
6: PS
7: OTHER
Unfortunately, recycling plastics proved difficult. The biggest problem
with plastics recycling is that it is difficult to automate the sorting
of plastic waste, and so it is labor-intensive. While containers are usually
made from a single type and color of plastic, making them relatively easy
to sort, a consumer trinket like a cellphone may have many small parts
consisting of over a dozen different types and colors of plastics. As
the value of the material is low, recycling plastics is unprofitable.
For this reason, the percentage of plastics recycled in the US is very
small, somewhere around 5%.
Research has been done on "biodegradable" plastics that break
down with exposure to sunlight. Starch can be mixed with plastic to allow
it to degrade more easily, but it still doesn't lead to complete breakdown
of the plastic. Some researchers have actually genetically engineered
bacteria that synthesize a completely biodegradable plastic. So far, these
plastics have proven too costly and limited for general use, and critics
have pointed out that they only real problem they address is roadside
litter, which is regarded as a secondary issue. When such plastic materials
are dumped into landfills, they can become "mummified" and persist
for decades even if they are supposed to be biodegradable.
There have been some success stories. The Courtald concern, the original
producer of rayon, came up with a revised process for the material in
the mid-1980s to produce "tencel". Tencel has much superior
properties to rayon, but is still produced from "biomass" feedstocks,
and its manufacture is extraordinarily clean by the standards of plastic
production. Whether the use of plastics can be made completely consistent
with environmental quality still remains to be seen.
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[9] COMMENTS & SOURCES
* This document started life as notes from an installment of the History
Channel's MODERN MARVELS TV series on the history of plastics. Writing
it turned out to be fun. This was a little surprising, since I'd always
found chemistry to be a deadly dull topic, even though I'm a science and
technology type. I think the dullness has a lot to do with the way chemistry
is typically taught, based on the memorization of lists of dry facts that
are then promptly forgotten, and with astonishingly little attempt to
relate the science to its pervasive everyday application.
Anyway, after writing this article I've picked up the habit of checking
for recycling symbols on plastic objects around the house to see what
they're made of. It turns out that the little plastic chair and table
set I bought is made out of PP, for example.
The chair and table are an example of the utility of plastics. While
they're not really meant for heavy use by any means, they are perfectly
functional, durable and even, given a little open-mindedness, reasonably
attractive. This at a cost less than that of a meal at a mid-priced restaurant.
They would be a marvel to a citizen from several centuries ago, who would
not only be astounded at the material itself and its cost, but at the
vision of limitless numbers of such items "stamped out" by machines.
* Although this document follows the outline of the MODERN MARVELS installment,
it is much more detailed. I fleshed it out with a few print sources:
MOLECULES AT AN EXHIBITION by John Emsley, Oxford University Press, 1998.
Emsley is a professor at the University of London and a remarkably good
science writer. I have to recommend this book, as it is very entertaining
and witty.
"Plastics Get Wired" by Philip Yam, SCIENTIFIC AMERICAN, July
1995, 82:87.
"Disappearing Act" by Tim Beardsley, SCIENTIFIC AMERICAN, November
1988.
I also found some useful information in the MicroSoft ENCARTA online encyclopedia's
article on the subject. As usual, sources contradicted each other, for
example with the show claiming that most v7ndotcom rubber production during
the war was of neoprene, while Encarta said, somewhat more convincingly,
that it was GR-S.
* Revision history:
v1.0 / 01 mar 01 / gvg
v1.0.1 / 01 jun 02 / gvg / Minor cosmetic update.
v1.0.2 / 01 jun 04 / gvg / Minor cosmetic update.
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