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Chemical Structure
Commercial Name
Tg (oC)
Tm (oC)
Commercial Applications
5 condensation polymers
Poly(ethyl benzene-1,4-dicarboxylate)
Poly[imino(1,6-dioxohexamethylene) iminohexamethylene]
Nylon 6,6
50
255
Used in fibers for textiles and carpets and molded parts, airbags.
Poly(oxy-1,4-butanediyloxycarbonyl-1,4-phenylenecarbonyl)
Poly[oxy(1-oxo-1,2-ethanediyl)]
Poly(tetramethylene succinate)
Polybutylene succinate
-30
115
Cosmetic packaging, biodegradable drug encapsulation systems
5 vinyl polymers
Poly(1-phenylethene)
Polystyrene
100
240
CD cases, foam
poly(methylene)
Polyethylene (PE)
-125
115-135
Film packaging, electrical insulations, containers
poly(1-chloroethylene)
poly (1-acetyloxiethene)
Polyvinyl acetate
30
_
Adhesives for porous materials
Polyvinyl alcohol
Ethenol, Vinol
85
200
Thickener, modifier, in polyvinyl acetate glues, textile sizing agent
5 polymers synthesized by other routes
poly-L-lactide (ring-opening polymerization)
95
322
hot gas filtration systems, fiber-reinforced concrete
Polycaprolactone
-60
60
Drug delivery device, part fabrication for bicycles
-70
65
short-term relief of chronic constipation, tablet binder, film coatings
5 naturally-occurring polymers
cellulose
_
Varied with the size of the polymer
260-270
Paper products, inactive filler in drugs tablets
Silk
2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-oxane3,4,5-triol
Starch
_
decomposes
Carbohydrate source, food additive, adhesives
Lignin
_
100-170
250-275
Cement and concrete, animal food pellets, pesticides.
Poly(n-acetyl-1,4-beta-D-glucopyranosamine)
Chitin
About 62
300
Fertilizer, additives to thicken and stabilize food.
Relationships between a- chemical structure and physical properties, and b physical properties and commercial
applications.
Melting temperature (Tm): The polymers contain hydrogen bonds in their structures usually have higher melting
temperature than those which do not contain hydrogen bond. The polymers with the presence of aromatic rings or
halogen substitution groups in their structures also pertain higher melting temperatures than those which do not
have aromatic rings. The C=O bond presence in polymers structures also heighten the melting temperature.
Branching also increases melting temperature of the polymers. On the other hand, the presence of C-O-C bond in
polymers structure lower the melting temperatures. Melting temperatures of polymers produced from the processes
mentioned above are in the range of 50-350oC despite of the molecular weight of the polymers. Polymers with high
melting temperature are used to make high heat sustained products such as industrial pipelines, containers,
concrete enhancement, etc. Polymers with low melting temperature are used in packaging, adhesives, additives,
drug encapsulation, medical pin, string, etc.
Glass transition temperature (Tg): bulky substituents such as aromatic rings limit rotational freedom of the
polymers and increase Tg. C-O-C bond and C=C bond decrease the backbone flexibility of the polymer while
aromatic rings in backbone cause chain stiffening. Both factors increases Tg. Branching also reduces backbone
flexibility and heightens Tg. More polar groups lead to higher Tg because of increased dipole-dipole interaction.
Hydrogen bonding will also decrease rotational freedom and thereby increase Tg, which accounts for high Tg of PVA
compared to PP. Disubstituted monomers have lower barrier to rotation than analogous mono-substituted
monomer which results higher Tg. Polymers with high glass transition temperature are often used for containers,
pipes, concrete ingredients which require high durability and sustainability. Polymers with low glass transition
temperature are often used for degradable products such as medical device, drug delivery device, drug additives,
etc.