Page 2 :
CHEM3020: POLYMER CHEMISTRY-UNIT-3, UNIT 3 Crystallization and crystallinity, Crystallinity of Polymer: The structure of a polymer is, described in terms of crystallinity. Usually most of the, polymers are in amorphous in nature or semicrystalline. All of we know that a crystalline solid has, a sharp melting point and amorphous do not have a, sharp melting point., , (a) melting point (100% Crystalline)(b) glass, transition temperature (100% amorphous), , Crystalline solids have a definite shape with orderly arranged ions, molecules or, atoms in a three-dimensional pattern often termed crystal lattice with a uniform intermolecular forces., Amorphous solids are the shapeless, disordered, and irregular arrangement of the, constituent particles of a solid. Their inter-molecular forces are not the same, nor are, the distances between the particles., Polymeric material usually contains some crystalline part and some amorphous part.
Page 3 :
CHEM3020: POLYMER CHEMISTRY-UNIT-3, UNIT 3 Crystallization and crystallinity, When we slowly heat a polymer and increase the temperature, the polymers, changes from the glassy state to rubbery state and finally to the viscous state as they, are semi-crystalline (amorphous with some percentage of crystalline), , Degree of Crystallinity: Due to the large size, even a polymer of regularity of molecular, structure does not exists entirely in crystalline form. As solidification begins, the, viscosity of the polymer rises and molecules finds more and more difficulty in arranging, their long chain in the regular pattern required for crystal formation. In fact, polymers, have regions of crystallinity called crystallities, embedded in amorphous material., Crystallities provides hardness and the amorphous region provide flexibility to the, polymeric material.
Page 4 :
CHEM3020: POLYMER CHEMISTRY-UNIT-3, , Degree of crystallinity, Degree of Crystallinity: The density of a crystalline polymer is greater than that of a noncrystalline polymer because of more efficient packing. The degree of crystallinity is the, measure of the amount of crystalline part in a polymeric sample. So, degree of, crystallinity is quantity which provides a measure of how much crystalline material is, present in a given polymer sample., One of the common methods for measuring the degree of crystallinity of the semi, crystalline polymers is the density method. In this method the densities of the, crystalline and amorphous polymer samples as well as the crystalline, as well as the, semi crystalline sample their densities are used to get an estimate of the degree of, crystallinity., ππ/( ππ β ππ), ππππππ‘πππ ππ πππ¦π π‘πππππππ‘π¦ =, π₯ 100, ππ /( ππ β ππ), Where,, pc- density of perfectly crystalline polymer;, Pa β density of amorphous polymer;, Ps- density of the specimen whose percentage of crystallinity is to be determined)
Page 5 :
CHEM3020: POLYMER CHEMISTRY-UNIT-3, , Degree of crystallinity, Factors influence Crystallinity, , (i) Molecular Weight: With increase in molecular weight of a polymer, % crystallinity, increases due to the large number of entanglement of chain which impose restriction, for unlimited growth of a crystallite., (ii) Symmetry of the repeating unit: Symmetrical repeat unit structure like-CH2- facilitates, the formation of crystallites. Random copolymers do not crystallize because there is no, regularity of the repeat unit. Geometrical regularity is also desired in a polymer for it, to show crystallinity. For example, only the configurationally regular forms ( isotactic, and syndiotactic) of polyproplylene can crystallize but atactic polypropylene is, amorphous., (iii) Chain Branching: High density polypropylene has almost perfectly linear structure and, therefore it can be obtained in a highly crystalline state ( 80-85% crystallinity) with high, melting point ( 133-1350C). Low density polyethylene has number of short chain (ethyl, and butyl) and long chain branches. So, it can not be obtained in a highly crystalline, state ( 55% crystalline) and melting point is also low ( 110-1150C)., (iv) Cross Linking: A polymer with high cross-linked density is devoid of crystallinity, because the presence of a dense array of cross-links effectively eliminate crystallinity
Page 6 :
CHEM3020: POLYMER CHEMISTRY-UNIT-3, Factors affecting crystalline melting point., , Affect of Crystallinity on properties of polymer:, With increase in % crystallinity(i) Strength and stiffness of polymer increases but brittleness also increases., (ii) Solubility and permeability of polymer decreases, (iii) Density and melting point of polymer decreases, (iv) Opacity of the polymer also increases., Factors affecting Crystalline melting point Tm:, (i) Cain flexibility: Higher flexibility, lower Tm. The presence of double bond, and aromatic group in the polymeric backbone lowers the flexibility, thus, increases Tm., (ii) Size and type of side groups: Bulky or large side groups tends to restrict, molecular rotation and raise Tm., (iii) Presence of Polar Groups: Polar groups (Cl, OH, CN) in main chain,, Hydrogen bonding within the crystal raise Tm., (iv) Degree of Branching: Side branching introduces defects into the crystalline, materials, hence lowers Tm.
Page 7 :
CHEM3020: POLYMER CHEMISTRY, , UNIT-4, , Glass transition Temperature(Tg) of polymers, Glass transition temperature (Tg) and Factors affecting glass transition temperature (Tg), When plastic or rubber is cooled up to certain temperature,, it becomes so hard and brittle that it breaks into pieces on, application of stress. The temperature below which the, polymer becomes hard, brittle and glassy and above which, it is softener and flexible, is known as glass transition, temperature (Tg). The glass transition is a property of only, amorphous portion of a semi-crystalline solid. The, crystalline portion remains crystalline during the glass, transition, When a polymer is heated beyond Tg, it passes from glassy, state to rubbery state. Further heating much above, causes, melting of the polymer and it starts flowing. The, temperature below which the polymer is in rubbery state, and above which it is a liquid is called melting temperature, of the polymer.
Page 8 :
CHEM3020: POLYMER CHEMISTRY, , UNIT-4, , Glass transition Temperature(Tg) of polymers, Glass transition temperature (Tg) and Factors affecting glass transition temperature (Tg)
Page 9 :
CHEM3020: POLYMER CHEMISTRY-UNIT-3, , Glass transition Temperature(Tg) of polymers, , Glass transition temperature (Tg) and Factors affecting glass transition temperature (Tg)
Page 10 :
CHEM3020: POLYMER CHEMISTRY, , UNIT-4, , Glass transition Temperature(Tg) of polymers, Factors affecting glass transition temperature (Tg), 1) Chain Flexibility and Rigidity: Stiffening groups in the polymer chain reduce the, flexibility of the chain and raise the value of Tg . In other words, greater the intrinsic chain, flexibility, smaller will be the Tg., Example: Tg ( PP) Tg (PE), Since substitution of H in PE by CH3 group in PP impedes the, rotation about a C-C single bond. Thus, Tg is affected by the, nature of substitution, , Polyethylene (PE), , Polypropylene (PP), , Example: Configuration, Tg ( PE) Tg (Cis-1,4-polybutadiene), Because inclusion of a double bonds stiffen the chain at the point of, inclusion but at the same time increases the flexibility of the adjacent bonds., , Cis-1,4-polybutadiene, , 2) Intermolecular Forces: Tg (PE) < Tg ( PVC or Tg (Nylon, 66), Stronger intermolecular forces due to dipole forces, H-bonding, etc. decreases the mobility of the chain lead to a higher Tg. PVC, has stronger intermolecular forces than polypropylene because, of the dipole-dipole forces from the C-Cl bond., , Nylon 66, Polyvinyl chloride (PVC)
Page 11 :
CHEM3020: POLYMER CHEMISTRY, , UNIT-4, , Glass transition Temperature(Tg) of polymers, Factors affecting glass transition temperature (Tg), 3) Molecular Weight: Glass transition temperature, Tg is directly proportional to, molecular weight of the polymer., 4) Pendant Groups: The influence of pendant groups on the glass transition temperature, is somewhat more complicated. Bulky pendant groups, such as a benzene ring, can catch, on neighboring chains like a "fish hook" and restrict rotational freedom and can, increases Tg., 5) Cross-Linking: The presence of cross-links between chains restricts rotational motion, and hence, greater the degree of cross-linking , the higher the Tg., 6) Plasticizers: Plasticizers are low molecular weight compounds added to plastics to, increase their flexibility and workability. They weaken the intermolecular forces between, the polymer chains as it increases the mobility and decrease Tg., , 7) Copolymerization: Random copolymers have lower Tgβs since it tends to promote the, disorder, reduce molecular packing and reduces the inter chain forces of attraction.
Page 12 :
CHEM3020: POLYMER CHEMISTRY-UNIT-3, Factors affecting glass transition temperature, , Significance of Tg, , directly proportional to molecular weight of polymer., directly proportional to degree of cross links, Glass transition temperature, , directly proportional to intermolecular force., directly proportional to number of side groups, inversely proportional to flexibility., inversely proportional to plasticization.
Page 13 :
CHEM3020: POLYMER CHEMISTRY, , UNIT-4, , Glass transition Temperature(Tg) of polymers, Determination of Tg and free volume concept:, Glassy State, , Viscofluid State, , As per thermodynamic view point, Tm is a first order, transition because there is an abrupt change in a, fundamental property such as specific volume with, temperature. However, Tg is a second order transition as, only the first derivative of such properties changes. For the, determination of Tg and Tm, the specific volume of a semicrystalline polymer sample is measured as a function of, temperature., The plotting of data yields the curve shown in figure., , Viscoelastic State, , Crystallinity ---- Transition temperature, 0%----------------only Tg, 100%-------------Only Tm, , Free volume Concept: At high temperature, the semi-crystalline polymer is in fluid state, and polymeric molecules adopt random configurations. As the temperature decreased, the, specific volume of the polymer also linearly decreased before Tm. But after, Tm, further, decrease in temperature leads to rapid decrease in specific volume. This is because, crystallization occurs and crystals are significantly denser.
Page 14 :
CHEM3020: POLYMER CHEMISTRY, , UNIT-4, , Glass transition Temperature(Tg) of polymers, Free volume theory:, Near Tg, the slope of the curve changes, below, Tg, if the temperature is further lowered further, contraction takes place through the amorphous region. Below Tg, the polymer is in solid physical, state and molecules have amorphous and crystalline region. The concept of free volume can be, used to analyze the glass transition. The free volume is a space in a solid or liquid sample which is, not occupied by the polymer molecules, i.e. the empty space between molecules. Above Tg, the, free volume is high so, polymer molecules can change conformations freely., As the temperature of the melt lowered, the free volume will, reduce eventually there will not be enough free volume to, allow the molecular rotation of translation to take place. The, temperature at which this happens corresponds to Tg as, below this temperature, the polymer glass is effectively frozen, , Below Tg- free volume is constant and above Tg- free volume increases with temperature
Page 15 :
CHEM3020: POLYMER CHEMISTRY, , UNIT-4, , Glass transition Temperature(Tg) of polymers, Williams-Landel-Ferry (WLF) Equation: A general empirical formula has been, formulated and known as Wiliams-Landel-Ferry equation describing the dependence, of molecular structure for the relation between aΟ and absolute temperature- given by,, , Where aΟ is known as shift factor., In glassy state, large scale molecular motion does not take place, rather atoms and small, groups of atoms move against the local restraints of secondary bond forces, much as, atoms vibrates around their equilibrium position in crystal lattice. The glass transition state, corresponds to the onset of liquid like motion of much longer segments of molecules.,, characteristic to rubbery state. This motion requires more free volume than the short, range movements of atoms in the glassy state. The rise in relative free volume with, increasing temperature above Tg leads to the higher observed volume expansion, coefficient in this region. Since fully extended chain is the conformations of minimum, energy, it tends to be assumed more frequently as the temperature is lowered. As the, molecule thus straightened out, the free volume decreases and flow becomes more, difficult.
Page 16 :
CHEM3020: POLYMER CHEMISTRY-UNIT-3, , log Ξ·, , WLF equation, WLF equation: Williams-Landel-Ferry Equation-Explaination, The empirical Williams-Landel-Ferry equation describes the temperature dependence, of the viscoelastic properties of polymers., The temperature dependence of the viscosity may, be described by an Arrhenius equation of the form, , The two parameters E and A are usually determined from a plot of log Ξ· against, 1/T which yields a straight line:, , Doolittle postulated that the viscosity is an exponential function of the reciprocal, of the fractional free volume f, , where A and B are constants and f is the free volume fraction.
Page 19 :
References and suggestions for, further reading:, , 1. Textbook of Polymer Science by, Fred W. Billmeyer, Wiley, 2. Polymer Chemistry by Charles E, Carraher, Jr., Marcel Dekker, Inc., 3. Principle of Polymerization by, George Odian, Wiley
Page 20 :
THANK YOU
