This is followed by discussion of the morphologic features of the polymer
single crystal and those of polymers crystallized from the melt.
1. Crystal Structure of Polymers
• Crystallinity depends on the molecular structure of polymers.
• No bulk polymer is completely crystalline
• In semi-crystalline polymers, regular crystalline units are linked by
un-orientated, random conformation chains (amorphous regions)
Influence of morphology on properties
Polymers with higher crystallinity are denser, stiffer, harder, tougher and
more resistant to solvents.
Amorphous domains add flexibility and promote ease of processing below
the melting temperature.
Polymer structures
A: Linear, amorphous
B: Linear, semi-crystalline
C: Branched, amorphous
D: Slightly cross-linked
E: Cross-linked
F: Linear ladder structure
2. Morphology of Polymer Single Crystals Grown from Solution
Chain folded-model
-Many polymers crystallize as very thin platelets (or lamellae)
-Idea – the chain folds back and forth within an individual plate (chain
folded model)
Fringed-micelle structure: Suitable for natural polymers such as cellulose
and proteins that consist of fibrils. The molecules passed successively
through a number of these crystalline and intervening amorphous region
•The crystallites were pictured as sheaves of chains aligned in a parallel
fashion
Morphology of Polymers Crystallized from Melt
More commonly, many polymers that crystallize from a melt form
spherulites
One way to think of these – the chain folded lamellae have amorphous “tie
domains” between them
These plates pack into a spherical shape
• Ordinary tie-molecules bond two crystalline parts together across the
amorphous part. Two chains can also be entangled together by a physical bond
(entanglement)
Polymer structure hierarchy
Spherulites
• Following crystallization from the melt or concentrated solution,
crystallites can organize into spherical structures called spherulites
• Each spherulite contains arrays of lamellar crystallites that are typically
oriented with the chain axis perpendicular to the radial (growth) direction
of the spherulite
Spherulite nucleation and growth
• Formation of nuclei
• Accelerated crystallization: spherulites grow in radius
• Crystallization slows: spherulites begin to touch each other
• Crystallinity may still increase very slowly
What encourages crystallinity
A polymer’s chemical structure determines whether it will be crystalline
or amorphous in the solid state
Symmetrical chain structures favor crystallinity by allowing close
packing of polymer molecules in crystalline lamellae
Tacticity and geometric isomerism (i.e. trans configuration) favor
crystallinity
Branching and atacticity prevent crystallization
Crystallinity and the effect of hydrogen bonding
Specific interactions (hydrogen bonding between chains) enhance
crystallinity.
Within nylons, hydrogen bonding between;
Amide carbonyl group on one chain
Hydrogen atom of an amide group of another chain
Conformation and configuration of polymer chains in the lamellae
For many polymers, the lowest energy conformation is the extended
chain or planar zig-zag conformation (for example PE, polymers capable
of hydrogen bonding).
For polymers with larger substituent groups, the lowest energy
conformation is a helix (for example in PP, three monomer units form a
single turn in the helix).
Growth of the spherulites
At t0 the melt begins to cool
At t4 the sample is full of spherulites