In polymer physics, spherulites (from Greek sphaira = ball and lithos = stone) are spherical semicrystalline regions inside non-branched linear polymers. Their formation is associated with crystallization of polymers from the melt and is controlled by several parameters such as the number of nucleation sites, structure of the polymer molecules, cooling rate, etc. Depending on those parameters, spherulite diameter may vary in a wide range from a few micrometers to millimeters. Spherulites are composed of highly ordered lamellae, which result in higher density, hardness, but also brittleness when compared to disordered regions in a polymer. The lamellae are connected by amorphous regions which provide elasticity and impact resistance. Alignment of the polymer molecules within the lamellae results in birefringence producing a variety of colored patterns, including a Maltese cross, when spherulites are viewed between crossed polarizers in an optical microscope.

Formation

If a molten linear polymer (such as polyethylene) is cooled down rapidly, then the orientation of its molecules, which are randomly aligned, curved and entangled remain frozen and the solid has disordered structure. However, upon slow cooling, some polymer chains take on a certain orderly configuration: they align themselves in plates called crystalline lamellae.

Spherulite (polymer physics)

Growth from the melt would follow the temperature gradient (see figure). For example, if the gradient is directed normal to the direction of molecular alignment then the lamella growth sideward into a planar crystallite. However, in absence of thermal gradient, growth occurs radially, in all directions resulting in spherical aggregates, that is spherulites. The largest surfaces of the lamellae are terminated by molecular bends and kinks, and growth in this direction results in disordered regions. Therefore, spherulites have semicrystalline structure where highly ordered lamellae plates are interrupted by amorphous regions.

Spherulite (polymer physics)

The size of spherulites varies in a wide range, from micrometers up to 8 centimeter and is controlled by the nucleation. Strong supercooling or intentional addition of crystallization seeds results in relatively large number of nucleation sites; then spherulites are numerous and small and interact with each other upon growth. In case of fewer nucleation sites and slow cooling, a few larger spherulites are created.

Spherulite (polymer physics)

The seeds can be induced by impurities, plasticizers, fillers, dyes and other substances added to improve other properties of the polymer. This effect is poorly understood and irregular, so that the same additive can promote nucleation in one polymer, but not in another. Many of the good nucleating agents are metal salts of organic acids, which themselves are crystalline at the solidification temperature of the polymer solidification.

Properties

Mechanical

Formation of spherulites affects many properties of the polymer material; in particular, crystallinity, density, tensile strength and Young's modulus of polymers increase during spherulization. This increase is due to the lamellae fraction within the spherulites, where the molecules are more densely packed than in the amorphous phase. Stronger intermolecular interaction within the lamellae accounts for increased hardness, but also for higher brittleness. On the other hand, the amorphous regions between the lamellae within the spherulites give the material certain elasticity and impact resistance.

Changes in mechanical properties of polymers upon formation of spherulites however strongly depend on the size and density of the spherulites. A representative example is shown in the figure demonstrating that the strain at failure rapidly decreases with the increase in the spherulite size and thus with the decrease in their number in isotactic polypropylene. Similar trends are observed for tensile strength, yield stress and toughness. Increase in the total volume of the spherulites results in their interaction as well as shrinkage of the polymer, which becomes brittle and easily cracks under load along the boundaries between the spherulites.