Everything about Polyethylene totally explained
Polyethylene or
polythene (
IUPAC name
polyethene) is a
thermoplastic commodity heavily used in consumer products (notably the
Plastic shopping bag). Over 60 million tons of the material are produced worldwide every year.
Description
Polyethylene is a
polymer consisting of long chains of the
monomer ethylene (
IUPAC name
ethene). The recommended scientific name
polyethene is systematically derived from the scientific name of the monomer. In certain circumstances it's useful to use a structure–based nomenclature. In such cases
IUPAC recommends
poly(methylene). Upon applying extremely high pressure (several hundred atmospheres) to a mixture of ethylene and
benzaldehyde they again produced a white, waxy, material. Because the reaction had been initiated by trace
oxygen contamination in their apparatus the experiment was, at first, difficult to reproduce. It wasn't until 1935 that another ICI chemist,
Michael Perrin, developed this accident into a reproducible high-pressure synthesis for polyethylene that became the basis for industrial LDPE production beginning in 1939.
Subsequent landmarks in polyethylene synthesis have revolved around the development of several types of
catalyst that promote ethylene polymerization at more mild temperatures and pressures. The first of these was a
chromium trioxide-based catalyst discovered in 1951 by
Robert Banks and
J. Paul Hogan at
Phillips Petroleum. In 1953 the German chemist
Karl Ziegler developed a catalytic system based on
titanium halides and organoaluminium compounds that worked at even milder conditions than the Phillips catalyst. The Phillips catalyst is less expensive and easier to work with, however, and both methods are used in industrial practice.
By the end of the 1950s both the Phillips- and
Ziegler-type catalysts were being used for HDPE production. Phillips initially had difficulties producing a HDPE product of uniform quality and filled warehouses with off-specification plastic. However, financial ruin was unexpectedly averted in 1957 when the
hula hoop, a toy consisting of a circular polyethylene tube, became a fad among youth in the
United States.
A third type of catalytic system, one based on
metallocenes, was discovered in 1976 in Germany by
Walter Kaminsky and
Hansjörg Sinn. The Ziegler and metallocene catalyst families have since proven to be very flexible at copolymerizing ethylene with other
olefins and have become the basis for the wide range of polyethylene
resins available today, including
very low-density polyethylene and
linear low-density polyethylene. Such resins, in the form of fibers like
Dyneema, have (as of 2005) begun to replace
aramids in many high-strength applications.
Until recently the metallocenes were the most active single-site catalysts for ethylene polymerisation known—new catalysts are typically compared to zirconocene dichloride. Much effort is currently being exerted on developing new, single-site (so-called
post-metallocene) catalysts that may allow greater tuning of the polymer structure than is possible with metallocenes. Recently work by Fujita at the
Mitsui corporation (amongst others) has demonstrated that certain salicylaldimine complexes of
Group 4 metals show substantially higher activity than the metallocenes.
Physical properties
Depending on the
crystallinity and
molecular weight, a
melting point and
glass transition may or may not be observable. The temperature at which these occur varies strongly with the type of polyethylene. For common commercial grades of medium- and high-density polyethylene the melting point is typically in the range 120 to 130 °C ((250 to 265 °F). The melting point for average, commercial, low-density polyethylene is typically 105 to 115 °C (220 to 240 °F).
Most LDPE, MDPE and HDPE grades have excellent chemical resistance and don't dissolve at room temperature because of their crystallinity. Polyethylene (other than cross-linked polyethylene) usually can be dissolved at elevated temperatures in
aromatic hydrocarbons such as
toluene or
xylene, or in chlorinated solvents such as
trichloroethane or
trichlorobenzene.
Environmental issues
The wide use of Polyethylene makes it an important environmental issue. Though it can be
recycled, most of the commercial Polyethylene ends up in landfills and in the oceans (Notably the
Great Pacific Garbage Patch). Polyethylene isn't considered
biodegradable, as it takes several centuries until it's efficiently degraded. Recently (May 2008) Daniel Burd, a 16 year old Canadian won the
Canada-Wide Science Fair in Ottawa after discovering that
Sphingomonas, a type of bacteria, can degrade over 40% of the weight of plastic bags in less than three month. The applicability of this finding is still a matter for the future.
Further Information
Get more info on 'Polyethylene'.
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