P. 1
reologie polimeri

reologie polimeri

|Views: 11|Likes:
Published by Alina Gabriela Rusu

More info:

Published by: Alina Gabriela Rusu on Mar 25, 2013
Copyright:Attribution Non-commercial


Read on Scribd mobile: iPhone, iPad and Android.
download as PDF, TXT or read online from Scribd
See more
See less





Polymer Rheology

P Sunthar

Abstract This chapter concerns the flow behaviour of polymeric liquids. This is a short introduction to the variety of behaviour observed in these complex fluids. It is addressed at the level of a graduate student, who has had exposure to basic fluid mechanics. The contents provide only a broad overview and some simple physical explanations to explain the phenomena. For detailed study and applications to industrial contexts the reader is referred to more detailed treatises on the subject. The chapter is organised into three major sections

1 Phenomenology
Interesting behaviour of a material is almost always described by first observing and extracting the qualitative features of the variety of phenomena exhibited. To a novice, this is the place to start. Some questions to ask would be: What makes this phenomena different? How to depict it in terms of a simple model? Is there a “law” that can describe the behaviour? Are there other phenomena that obey similar laws? What role has this played in the state of the universe? Can it be employed for the betterment of quality of life? What are the consequences of this behaviour to processes that manipulate or use the material? Some of these are simple questions, answers to which may not solve any urgent and present problem. However, it puts it in a larger context. Often, when solving difficult problems in rheology using advanced methods and tools, one tends to miss simple laws exhibited by the materials in reality, knowing which may help in getting an intuitive feel of the solution, and thereby a faster approach to the answer.

Department of Chemical Engineering, Indian Institute of Technology (IIT) Bombay, Mumbai 400076 India. e-mail: p.sunthar@gmail.com



P Sunthar

1.1 What are Polymeric Liquids?
Polymeric liquids are precisely what the name states: namely they are like the liquids we know that flow and have as constituents, some or all being long chain molecules or polymers. The conventional definition used to define simple liquids: that they do not support shear stress at rest, cannot be used to define the liquid state of a polymeric liquid. This is because polymeric liquids, like most other liquids described in this book are complex fluids: They exhibit both liquid and solid like behaviour, and some of their dynamic properties may not be thermodynamic constants but some effective constant dependent on the history of forces acting on it. An example is a “viscosity” which is a function of shear rate, or a “viscosity” that changes with time.

1.1.1 Chemical Nature The common feature of all polymeric liquids considered in this chapter are that they have long chain of monomers joined by chemical bonds. They could even be oligomers or very long chain polymers. Most of them have large molecular weights more than a 1000 and up to about 109 . Many materials we use today are polymers or blends of polymers with other materials. In some stage of their processing most of them were in one liquid state or other: as solutions or pure molten form.

1.1.2 Physical Nature The chief physical property of a polymer that distinguishes itself from other fluids that exhibit complex behaviour is the linearity of the chain. It is not the high molecular weight that leads to the peculiar phenomena but that it is arranged linearly: The length along the chain is much larger that the other dimensions of the molecule. For example, a suspension of polystyrene beads (in solid state) may have high molecular weight per bead. But it may exhibit rheological properties of a suspension rather than a polymer solution. This is because for most properties that we measure, such as the viscosity, it is the beads spherical diameter that matters, and not the molecular weight per bead. There is no linear structure that is exposed to these measurements. On the other hand a solution of polystyrene molecules in cyclohexane is a polymeric liquid.

What is the difference between a polymeric liquid to us and a huge bowl of noodles to a Giant? A huge bowl of noodles is very much like a several molecules of polymers put together. Just as we “see” polymers, so the bowl with these noodles would appear to a Giant. The noodles have the necessary linearity, they are flexible like the polymers are, and as a whole can take the shape of the container they are put into. Can we

This is like a noodle-state. such as the polymer itself. extruders. This state is called the dilute solution. Many of the properties of polymeric liquids we observe. Between these two states of pure and dilute. which in many cases are polymers. or other polymers.Polymer Rheology 3 then use a model bowl full of noodles to understand the behaviour of polymeric liquids. The primary question is how is the flow modified in the presence of these long chain macromolecules. Increasing the concentration of the additive polymer from dilute values. 1. moulds. are due to the random linear translating motion of its constituents. spinnerets.. In the polymer processing field one needs to know. Parts of the polymer’s motion influences other parts of the same chain. such as that it flows. to the extent that has even earned a Nobel Prize in Physics for Pierre-Gilles de Gennes in 1991. It is equivalent to one polymer because the solution is so dilute that the motion of one polymer does not influence the other polymers in solution. of liquids by having additives. Take a pure polymer (with no other additives) to a high enough temperature that it is molten. The other extreme of this state is when small amounts of a polymer is added as an additive (solute) to a solvent. It is the random motion along the length of the chain and the resulting influence on the other constituents of the material. Not entirely! The key difference between the two systems is temperature or random motion. For consumer products. This is very similar to putting one polymer chain in a sea of solvent. we would like to able to control the feel. etc. The molten state is like a dry noodle with full of entanglements. rates. . how to control the flow and stability of these liquids as they pass through various mixers. etc. on the other hand. shapes. solvent. as in any fluid mechanics problem. that are addressed by a wide variety of engineers and physicists. These fields have provided (and continue to provide) with several problems. Further increase in concentration leads to the concentrated-solution where there are significant overlaps and entanglements (like in an entangled noodle soup).2 Who needs to study flow of polymeric liquids? The primary motivation to study polymeric fluids comes from industrial and commercial applications: Polymer processing and consumer products. we can have a range of proportions of the polymer and the other component. we get to the semi-dilute region where the polymers are distributed in the solution such that they just begin to “touch” each other. that leads to the defining properties of polymeric liquids. “States” of Polymeric Liquids The simplest definition (though not a theoretically simpler model to handle) of a polymeric liquid state is the molten state. except that the polymers are in continuous motion. similar as in simple liquids.

Viscosity is measured in Pa-s (Pascal second). σxy η= (1) ˙ γ ˙ is the shear rate (applied where σxy is the shear stress (measured or applied) and γ or measured). . as it is related to the amount of recoverable energy stored by the deformation.4 P Sunthar 1. In the following section we sample a few defining behaviours of various properties in commonly encountered flows. with the hope that the knowledge gained can be appropriately used in a complex flow pattern. Rheology involves measurements in controlled flow. materials that exhibit weak elastic properties. We have several components in a shampoo. not only because the geometries are complex. G for most polymeric fluids is in the range 10–104 Pa. or vice versa. are also known as soft matter. mainly the viscometric flow in which the velocity gradients are nearly uniform in space. but also because the constituents are not usually simple. Complex fluids also exhibit elastic behaviour. namely the elasticity. performing various actions. The modulus of elasticity is defined as G= σxy γ (2) where γ is called the strain or the angle of the shearing deformation. G is measured in Pa (Pascal). They are called viscometric as they are used to define an effective shear viscosity η from the measurments. This is why complex fluids. Even when a theoretical model of the reason for the behaviour is not known. rheological measurements provide useful insights to practising engineers on how to control the flow (η ) and feel (G) polymeric liquids. of which polymeric fluids form a major part.e. i. In these simple flows. known as the storage modulus. The word Rheology is defined as the science of deformation and flow. This brings in the need to study the behaviour of polymeric liquid in simple flows and for simple systems. but also about another important property. which is much smaller than that of solids (> 1010 Pa). Akin to the viscosity defined above being similar to the definition of a Newtonian viscosity. the Hookean solid. as polymers are rarely synthesised in a sharp monodisperse population. Molecular weight distribution of a polymer is another level of complexity. G is one of the elastic modulii. there is an applied force where the velocity (or the equivalent shear rate) is measured. the elasticity of a complex material can be defined similar to its idealised counter part. Rheology is not just about viscosity. In the following sections we present a broad overview of the variety of phenomena observed in polymeric liquids and how the rheological characterisation of the liquids can be made. Rheological measurements on polymers can reveal the variety of behaviour exhibited even in simple flows.3 What is Polymer Rheology? Clearly industrial flows are complex. was coined by Prof Bingham in 1920s [1].

3 Contraction Flow Sudden contraction in the confining geometry leads to very different streamline patterns in polymeric liquids. Whereas in polymeric liquids. including in dilute polymer solutions.Polymer Rheology 5 1.1 Weissenberg Rod Climbing Effect When a liquid is stirred using a cylindrical rod. different patterns of secondary flow are observed. Rod climbing is exhibited by liquids that show a normal stress difference.2 Extrudate or Die Swell This phenomenon is observed when polymeric melts are extruded through a die.4. upon application of shear flow. the accumulated stress difference tends to push the fluid in the gradient direction. In contrast in a Newtonian liquid. As the fluid exits the die to form a free surface with the surrounding air. These include large vortices and other instabilities. so long as there is a continuous rotation. The diameter of liquid as it exits a circular die can be three times larger that the diameter of the die.4. We describe a few of them here and provide links to resources where they may be viewed. whereas polymeric liquids. . These are best seen in recorded videos. there is a dip in the surface of the liquid near the rod. 1. no secondary flows are observed. One of the important reasons for this phenomena is again the normal stress difference induced by the shear flow in the die. 1. whereas in the case of Newtonian fluids it is just about 10% higher in the low Reynolds number limit.4. In Newtonian liquids at low Reynolds number. 1. These flows are undesirable in many situations in polymer processing as it leads to stagnation and improper mixing of the fluid in the vortices. There are many more phenomena discussed and illustrated in [2]. In Newtonian liquids the normal stresses (pressure) are isotropic even in flow.4 Visual and Measurable Phenomena Some of the striking visual phenomena are associated with flow behaviour of polymeric liquids. the liquid that wets the rod begins to “climb” up the rod and the interface with the surrounding air assumes a steady shape dangling to the rod. begin to develop normal stress differences between the flow (τxx ) and flow-gradient directions (τyy ).

1. and the viscosity of such systems are usually large that it is not common to encounter large Reynolds number flows that lead to turbulence.4 Tubless Siphon In a typical syphoning experiment. But this is the case in Newtonian liquids. turbulence can be easily observed. This phenomenon has been used in transportation of liquids and in fire fighting equipment.5 Relaxation time and Dimensionless Numbers One of the simplest and most important characters of polymeric liquids is the existence of an observable microscopic time scale. Since many visually observable and processing time scales are of similar order. the top portion of the cut liquid recoils back into the jar.4.4. a tube filled with liquid drains a container containing the liquid at a lower pressure. The interesting feature of such turbulent flows. 1.6 Turbulent Drag Reduction In most of phenomena discussed so far the concentration of the polymer was about 0. When the tube is lifted off the surface of the liquid.1% or higher. the ratio of these time scales becomes important. In the case of polymeric liquids. The large scale microscopic motions are usually associated with the elastic character of the polymeric liquids. For regular liquids the timescales of molecular motion are in the order of 10−15 seconds. in the liquid they are suspended in (solutions or melts).4. the flow immediately stops. the liquid continues to flow with a free surface with the air without the tube. Very similar to a sheet of elastic solid. as the tube is taken of the surface. even though the tube goes higher than the liquid surface. In the chapter on polymer physics there is a discussion of the relaxation times. upto nearly five times.6 P Sunthar 1.5 Elastic Recoil A “sheet” of polymeric liquids pouring down from a vessel can be literally cut with a pair of scissors. .01% where the solution viscosity is not significantly enhanced above the solvent’s viscosity. The relaxation time is the time associated with large scale motion (or changes) in the structure of the polymer. there is an important timescale associated with large scale motions of the whole polymer itself. 1. at least in pipe geometries is that the turbulent friction on the walls is significantly less. apart from this small time scale. we denote this time scale by λ . associated with molecular translation. This could be from microseconds to minutes. In smaller concentrations of about 0. In polymeric liquids.

Weissenberg number is used only in situations where there is a homogeneous stretching of the fluid packet in the flow. are in which elastic effects are negligible.5. The other is a dynamic timescale associated with the motion of the fluid packets themselves. Therefore no unique strain rate can be associated with the flow. the macroscopic timescales may not be known a priori. In these cases it is customary to refer to the Deborah number defined as the ratio of the polymeric time scale to they dynamic or flow timescale De = λ td (4) For small De 1. etc. and so the fluid packet is said to have “no memory of its state” a few td back. For large Wi 1. or the time it spends in a particular secviscosity could alter the local shear rate γ tion td .1 Weissenberg Number The ratio of the microscopic time scale to the local strain rate is called as the Weissenberg Number ˙ ˙ or λ ε Wi = λ γ (3) Note that the strain rate is the inverse of the kinematic timescale. Most of the flow effects are seen around Wi ∼ O (1). as it is hardly observed in any practical application. To know the this dependence. The macroscopic time scales arises from two origins. the polymer has not sufficiently relaxed and the state a few td back can influence the motion of the packet now (because this can affect the local viscosity and hence the dynamics). 1. Such a flow is encountered only in viscometric flows and theoretical analysis. Examples are the time it takes for a fluid packet to transverse a geometry or a section. One is simply the kinematic local rate of stretching of the fluid packet (strain rate). and have to be determined as part of the solution. We denote this timescale by td . This means that they could have been subjected to various strain rates at various times in their motion. Except for viscometric flows.5. the polymer relaxes much faster than the fluid packet traverses a characteristic distance. the liquid behaves almost like an elastic solid. On the other hand for De ∼ O (1). we need to solve the fluid dynamic equations in the given geometry.2 Deborah Number In most practical applications the fluid packets undergo a non-uniform stretch history. 1. . For example the nature of the fluid’s ˙. That is the strain rates are uniform in space and time. pulsatile flow. Wi 1. This is measured by ˙ for extensional ˙ for shearing flows or the local elongation rate ε the local shear rate γ flows.Polymer Rheology 7 The microscopic timescale should be compared with the macroscopic flow time scales. Flows in which the Wi are small.

Study of linear viscoelastic properties can reveal information about the microscopic structure of polymeric liquids.e. meaning that the response is additive: effect of sum of two small deformations is equal to the sum of the two individual responses. thermodynamic forces tend to restore the equilibrium. Linear viscoelasticity was introduced in the chapter on Non-Newtonian Fluids. But polymeric fluids are not ideal elastic materials. This dependence is summarised in Table 1.7 of Ref. and the way experimental data is interpreted from measurements carried out at various temperatures (See section 8. the response of the system is linear. its relaxation time) depends on the linear size of the molecule. [3] for details). For small deformations. That is we cannot say that for a given molecular weight two different polymers will have the same relaxation time. Linear viscoelastic properties are associated with near equilibrium measurements of the system.3 Relaxation time dependence on Molecular weight Since the time large scale motion of the molecule (i.8 λchain ∼ M 2 λrep ∼ M 3. The scaling given for semi-dilute and entangled melts is only indicative of the longest relaxation time.8 P Sunthar Table 1 Scaling of the relaxation time λ of the polymeric liquid with molecular weight M for different classes of polymeric liquids [3]. When this microstructure is disturbed (deformed).0 λ ∼ M 1.6 Linear viscoelastic properties In general the elastic nature of a material is associated with some characteristic equilibrium microstructure in the material. 1. The dependence on molecular weight is not absolute. that is the configuration of polymers are not removed far away from their equilibrium structures. Restoration of these springs to their equilibrium state is through the elastic energy that is “stored” during the deformation process. The term rheology . Polymeric liquids have a microstructure that are like springs representing the linear chain. there are several relaxation process in these systems. It is only a scaling dependence for a class of polymeric liquids (We can only say that the relaxation time scales with molecular weight power some exponent). which is the viscous dissipation. The energy associated with this restoration process is the elastic energy. the molecular weight of a polymer has a direct bearing on the relaxation times. and they also have a dissipative reaction to deformation.5.4 1. Most of the models described in the “Polymer Physics” chapter deal with such a situation.5 λ ∼ M 1. Class Dilute solution in poor solvent Dilute solution in θ -conditions Dilute solution in good solvent Semi dilute solution Entangled Melts Scaling λ ∼ M 1.

at sufficiently small time scales. For dilute solutions. In these cases the viscosity obtained by extrapolating the viscosities obtained at accessible shear rates. Though all of the above tests can also be carried out in the non-linear regime. since the polymer contribution to the total viscosity is usually small. An important point to note here is that it is just not polymeric liquids that show elastic behaviour. 1. The zero shear rate viscosity is an important property to characterise the microstructure of polymeric liquid.Polymer Rheology 9 is used by physicists to usually refer to the linear response and by engineers to refer to the large deformation (shear or elongational) or non-linear state. values are typical order of magnitude approximations [4].1 Zero-shear rate viscosity The zero shear rate viscosity η0 is the viscosity of the liquid obtained in the limit of shear rate tending to zero. sequence of tests are carried out to ensure linear response. it is useful to define an intrinsic viscosity at zero shear rate as [η ]0 ≡ lim [η ] ≡ lim lim ˙→0 γ ˙→0 γ η − ηs c→0 c ηs (5) . as the limits of linear regime are not known a priori. Though the name suggests that it is a shear viscosity. We will first present aspects of the linear response before detailing the non-linear responses in the next sections. Creep A constant stress is applied and the deformation response is measured. but all liquids do. Liquid Water An Oil A polymer solution A polymer melt A glass Viscosity Relaxation time Modulus η (Pa. it is still in the linear response regime because the shear rate is approaching zero. Typical values of relaxation times and the elastic modulus for various liquids is given in Table 2.1 10 105 109 108 10 104 > 1010 Commonly used tests to study the linear response are Oscillatory Controlled stress/strain is applied in an small amplitude oscillatory motion and the response of the strain/stress is measured.1 1 105 > 1015 10−12 10−9 0.s) λ (s) G (Pa) 10−3 0. Table 2 Linear Viscoelastic properties of common liquids. Stress Relaxation A constant strain is applied and the decay of the stresses to the equilibrium value is studied.6. In practise it is not possible to attain very low shear rates for many liquids owing to measurement difficulties.

More details of this scaling can be found in Ref. under θ -conditions ηsp0 ∼ c2 and in the concentrated (and melt) regime (8) ηsp0 ∼ c14/3 (9) The scaling with respect to concentration in good solvents is weaker to about ∼ c1.10 P Sunthar λ (6) M where the scaling of λ is given in Table 1 for various types of dilute solutions. In semi-dilute regime. The plateau region is clear and pronounced in higher molecular weight polymers (with entanglements) in the concentrated solution or the melt states. as shown in Figure 3 [4]. The low frequency response (or long time response) is always viscous. 1.3 in semi-dilute and ∼ c3. The scaling behaviour is summarised in Figure 1. as defined in the NonNewtonian Fluids chapter. The symbols used here are the complex modulus G∗ : G for the storage component (real) and G for the loss component (imaginary).6. In this region the storage modulus (elastic) is always greater than the loss (viscous) modulus. G represents the characteristic elastic modulus of the system and G measures the viscous response. one is more interested in the scaling of the viscosity with concentration. In the semi-dilute regime.2 Oscillatory Response The typical response of a polymeric melt to an oscillatory experiment is shown in Figure 2. The usual way to report viscosity is through the specific viscosity (and not the intrinsic viscosity) [η ]0 ∼ The intrinsic viscosity scales as ηsp0 = η0 − ηs (7) The specific viscosity scales linearly with concentration in the dilute regime. The value of G at the plateau. The viscous regime behaviour is characteristic of all materials (including solids) showing Maxwell behaviour G ≈ η0 ω G ≈ G λ 2ω 2 (10) (11) . is known as the plateau modulus G0 N .7 in the concentrated. and is an important property in understanding the dynamics of the polymers in the melt state. The dominant elastic response is seen in the rubbery region where the storage modulus shows a plateau. At high frequencies the response is glassy (which is typically seen at temperatures around glass transition). [3].

This behaviour is also shown by polymeric liquids in the dilute and semi-dilute regimes. G λ= (12) G ω where G and G are measured in the viscous regime with the linear and quadratic scaling respectively. The characteristic relaxation time of the structured liquid can be obtained from the inverse of the frequency where G and G cross over in the flow transition regime. 1 Scaling of the specific viscosity ηsp0 with concentration of polymers. 11 Entangled log ηsp0 14/3 Semi− Dilute 2 Dilute 1 c∗ log c Fig. 2 Typical regimes in the complex modulus obtained using an oscillatory response of a polymeric liquid [5].Polymer Rheology Fig. As seen before. and η0 is the zeroshear rate viscosity. Therefore with increasing con- . increase in molecular weight increases the relaxation time. c∗∗ log(G ) Viscous Transition to Flow Rubbery/Plateau Glassy G’’ log(G ) G’ ∼ λ−1 log(ω) where. G is the elastic modulus (constant in the Maxwell model). so does the increase in concentration. The first transition denotes the semidilute regime and the second corresponds to the entangled regime.

The low frequency response of the loss modulus can also be used to obtain the zero-shear rate viscosity η0 from the Equation (11). Entangled melts show a plateau region. leading to the plateau region. The transition to the Maxwell behaviour is almost not seen due to limitations in observing very cycles. Cross-linked polymers have a wide and predominant plateau region [5].3 Stress Relaxation The relaxation of the stress modulus G(t ) in response to a step strain (for small strains) in the linear regime. The initial small time response of G(t ) is equivalent to the high frequency response of G∗ (ω ). which goes to the . close to the plateau region can also be used to distinguish the type of polymer melt. and the long time response is equivalent to the low frequency response. Unentangled melts do not have any plateau region. The low frequency response. P Sunthar log(G ) M log(ω) centration or molecular weight of the polymer.6. 3 Increase in the plateau region with increase in molecular weight. The link between the plateau region and the cross-linking suggests that the entanglement acts like a kind of constraint (like the cross-links) to the motion of the polymer contour.12 Fig. is equivalent to the oscillatory response G∗ (ω ). and directly make the transition to the Maxwell region. the intersection of the two curves shifts more and more towards the left (low frequencies). A schematic diagram of the plateau region behaviour of storage modulus G for various types of polymers is shown in Figure 4. 1. In small times a polymeric substance shows a glassy behaviour. just as in solids. A schematic diagram of the stress relaxation is shown in Figures 5 and 6 in linear and logarithmic scale respectively [5]. one being the Fourier transform of the other [6].

log G(t) G0 N log t plateau region (seen clearly in the logarithmic scale in Figure 6) and finally to the terminal viscous decay. the response can be understood as being highly elastic at small times. 4 Low frequency response of various type of polymers. which decays and begins to “flow” at large times: Given sufficiently long time any material flows. Since G is related to the elasticity. . 5 Stress relaxation in response to step strain in linear scale. 6 Stress relaxation in response to step strain in logarithmic scale. G(t) G0 N t Fig.Polymer Rheology Fig. log(G ) 13 Crosslinked Polymer Entangled Melt G0 N Unentangled Melt log(ω) Fig.

Figure 7 shows the decrease in the viscosity for two polymeric liquids. 1. They are called living polymers because they form and break along their length owing to thermodynamic and flow considerations. They are also known as worm like micelles. The viscosity defined in Equation (1) is a decreasing function of the shear rate. which are long linear structures formed from cylindrical liquid crystalline phases of micelles.14 Fig. their behaviour is very similar to a high molecular weight concentrated solution of polymers: large viscosity and elastic modulus. aligning in the shearing direction. The viscosity reduction upon shearing is therefore very significant and sharp in these systems.1 Shear Thinning Most polymeric liquids have their effective viscosity reduced upon shearing. However upon shearing they can break leading to the behaviour exhibited by low molecular weight counterparts. as depicted schematically in Figure 7. 7]. The shear thinning is not so much pronounced in dilute solutions as it is in concentrated solutions and melts [4. 7 Shear thinning of polymeric liquids is more pronounced in concentrated solutions and melts than in dilute solutions. At equilibrium. Examples of every day use are shampoo and shower gels which are very viscous at rest.7. Here we show the behaviour in flowing systems that produce significant deviations from the equilibrium microstructure. but can be easily flown out of the container by gravitational forces (which are sufficient to overcome the viscosity after they begin to flow).7 Flow Viscosity and Normal Stress So far we discussed the behaviour of polymeric liquids slightly disturbed from equilibrium. . in the linear regime. A special class of polymers is known as Living Polymers. 4 P Sunthar Concentrated solution log η 2 Dilute Solution 0 Worm−like Micelle −2 −5 −1 3 log γ ˙ 1.

blow moulding. y is the direction of the gradient and z is the vorticity direction. we can define two coefficients for the normal stresses: the only ˙2 . spinning of fibres. stagnation point flows. Though there are very few systems where it is purely extensional. The normal stress difference has two components N1 = τxx − τyy N2 = τyy − τzz (13) (14) where for planar Couette flow. because it is the lowest power of the shear difference is the denominator which is γ rate that the normal stresses depend on. there are several cases where there is significant elongation along with rotation of fluid elements. Polymeric liquids having microstructure can develop anisotropy in the orientation of the constituent polymers in flow. Ψ1 and Ψ2 defined as: N1 ˙2 γ N2 Ψ2 = 2 ˙ γ Ψ1 = (15) (16) The normal stress coefficients show shear thinning very similar to the viscosity.2 Normal stresses The normal stress difference is zero for a liquid that is isotropic. Elongational flows are encountered many situations. the absolute value for the normal stress difference can become larger than the shear stress as shown in Figure 8. breakup of jets or drops. however for very large shear rates. The simplest elongation is called as the uniaxial elongation the velocity gradient tensor for which is given by . x is the direction of flow. Such a behaviour is seen in concentrated solutions and in melts [4]. the two basic forms of fluid kinematics due to flow. Liquids being practically incompressible. 1. The second normal stress N2 is usually zero for polymeric liquids. which is a coefficient of the shear stress.7. there by leading to normal stress differences. etc. The coefficients are called as First normal stress coefficients. Similar to the viscosity.3 Elongational Flow Viscosity Extensional or elongational flow where the local kinematics dictates that the fluid element is stretched in one or more directions and compressed in others.Polymer Rheology 15 1. The normal stress behaviour shows a similar behaviour to that of shear stress.7. Sudden changes in flow geometry such as contraction or expansion. the elongational stretch conserves the volume.

like the shear viscosity is a function of the shear rate. is defined as ηE = σxx − σyy σxx − σzz = ˙ ˙ ε ε (18) The elongational viscosity. The elongational viscosity is defined as the asymptotic value of this coefficient for large times t → ∞. This phenomenon is called as strain hardening. it is difficult to measure the steady state + ˙) (t . The behaviour of the transient growth coefficients for various elongation rates is shown in Figure 9. The elongational strain is measured by the Henky strain defined as ˙ t = log ε =ε L(t ) L0 (19) . In experiments it is only possible to access a time dependent value ηE which is a transient elongational viscosity or more precisely the tensile stress growth coefficient [8]. in the case of elongational flows. P Sunthar N1 log σ. The elongational (or y and z directions. ε value. N1 σ log γ ˙   1 0 0 1 ˙ 0 − 2 0  ∇v = ε 0 0 −1 2 (17) which corresponds to stretching along the x direction and equal compression along ˙ is called the elongation or extension rate. 8 Comparison of the absolute values of normal stresses with thta of the shear stresses as a function of shear rate for concentrated solutions and melts.16 Fig. The elongational viscosity abruptly increases to a high value in short times [1]. However. ε tensile) viscosity.

Another useful way to report the elongational viscosity is the Trouton ratio [1]. This is because for a Hencky strain of ε = 7. which is defined as ηE (ε ) TR = √ (20) ˙) η( 3 ε √ ˙ (see further details ˙ = 3ε where the shear viscosity is measured at a shear rate γ in the chapter on Non-Newtonian Fluid Mechanics). It is not possible to easily measure the terminal or asymptotic value of the viscosity. and it could be the maximum or the value at the terminal Hencky strain. 10 Behaviour of the elongational viscosity with elongation rate for various polymeric liquids. or the value of the coefficient at a given experimentally accessible Hencky strain. log γ ˙ where L0 is the initial length of an element along the stretch direction and L(t ) is ˙t the deformed length that grows as L(t ) = L0 eε The elongational viscosity attains a maximum and then falls down. 9 Transient growth coefficient (trbansient elongational viscosity) for increasing ˙.Polymer Rheology Fig. It is a convention therefore to report the maximum + value of the transient tensile growth coefficient ηE as a function of the strain rate for practical applications. the elongation required is about 1100 times the initial value. log ηE Solutions ηE ×3 η Branched Melts Linear Melts log η log ˙ . For Newtonian (or inelastic liquids) the elongational viscosity is three times the shear viscosity. For polymeric . The elongational viscosity is not necessarily the steady state value. strain rates ε 17 log η+ E ˙ log t Fig. The behaviour of this viscosity is shown in Figure 10 for various polymeric liquids [4]. The “Steady values” of the viscosity reported are either the maximum values at a given strain rate.

depending on the molecular weight of the polymer the Trouton ratio can be several orders of magnitude higher than unity. The polymers in equilibrium have a coil like structure (see chapter on Polymer Physics). the viscosity can be related to the volume fraction. 2. such as the one shown in Figure 11 provide an indication of the extent of elongational viscosity effects in relation to the shear viscosity [4].18 Fig. 11 Trouton ratios for various polymeric liquids. and is given by the Einstein expression 5 η = ηs 1 + φ (21) 2 . 2 Modelling and Physical Interpretation Modelling in polymer rheology is mainly of two types: Phenomenological and molecular modelling. at low shear (and elongation) rates. The most dramatic effects are in dilute solutions of polymers where.1 Polymer solution as a suspension The simplest explanation of the polymeric liquid viscosity is that of a dilute solution. except that the particles are not spherical. the Trouton ratio TR is always TR ≈ 3. 1000 Dilute Solution P Sunthar log T R 100 Melts 3 Inelastic liquid 1/2 λ log ˙ . log γ ˙ liquids. The Trouton ratio plots. Dilute solutions show the most dramatic increase in the elongational viscosity. For dilute colloidal suspension the viscosity of the suspension is more than the solvent viscosity. A dilute solution is like a suspension of colloidal particles. Considering the polymer coils to represent colloidal particles. Some general phenomenological models have been discussed in the chapter on Non-Newtonian Fluid Mechanics. The basic molecular models have been discussed in the chapter on Polymer Physics: the Rouse and Zimm models [9]. Here we present some simple physical interpretations of the polymer rheological behaviour.

This results in an pervaded volume that is ellipsoidal and oriented towards the direction of flow. the extent of shear thinning is much more significant in concentrated solutions and melts in comparison with dilute solutions (see Figure 7).Polymer Rheology 19 where φ is the volume fraction of the colloidal particle. the coil like structure of the molecules assume a spherical pervaded volume. The Zimm theory predicts this constant to be 1. 2. on the average. whereas experiments and simulations incorporating fluctuating hydrodynamic interactions (without the approximations made in Zimm theory) observe the value to be Uη R = 1. upon shearing the chains begin to de-entangle and align along the flow. This is the reason for the high viscosity of the solution. the microstructure of the solution is like a network: the entanglements act like nodes of a covalently bonded network junctions which restricts the motion of the polymers and therefore of the solution. Because of this the increase in viscosity is reduced. The explanation for viscosity decrease in dilute solutions is subtle and involves several factors [9. 2. for spherical particles.3 Normal Stresses The existence of normal stresses in polymeric systems is due to the anisotropy induced in the microstructure because of flow. The restoring force is different in the two planes xx and yy. This constant is an universal constant for all polymers and solvents chemistry and depends only on the solvent quality (which could be poor. This can be easily understood in the case of dilute polymer solutions. . In the entangled state. The flow causes the molecules to stretch towards the direction of flow and tumble. In the absence of flow.66. because the shape of the coil changes continuously due to thermal Brownian forces from solvent). This approximation is valid in the limit φ → 0.2 Shear Thinning As noted before. or good solvents). We will restrict to simple explanations in entangled systems (i. in concentrated solutions and melts).5. Polymer coils are not rigid spheres. However.e. This reduces the viscosity. but behave more like a porous sphere (on the average. 7]. This results in the anisotropic normal forces. theta. For dilute polymers the viscosity can be written as η = ηs (1 + Uη R φ ) (22) where Uη R is a constant < 5/2.

5. Whereas upon elongation the chains are oriented in the direction of elongation. This leads to anisotropy and stress differences between the elongation and compression planes. The zero shear rate viscosity is itself much higher than the solvent viscosity. are disentangled and begin to orient along the extensional direction. Since the polymers are not infinitely extensible. The main reason for this is in the dilute state at equilibrium. At strain rates small compared to the inverse reptation time (or dis−1 . Fully Stretched . At higher strain rates ε volume of the polymers). the stress difference between the planes saturates to the value given by that in the fully stretched state (which is like a slender rod). P Sunthar Reptation Orientation Stretching log ηE τd log ˙ τR 2. the thermal fluctuations can no longer hold against the forces generated on the ends of the polymer due to flow. The chains then begin to stretch. for linear polymer melts.4 Elongational Viscosity As shown in Figure 11 dilute solutions have a dramatic effect on the elongational viscosity. when chain stretching begins (similar to the case in dilute polymer solutions). 12 Theoretical prediction of the elongational viscosity in the “standard molecular theory” or the tube model. the polymers are in a coil like state in a suspension whose viscosity is only slightly more than the solvent viscosity. After a critical elongation rate given by the Weissenberg number Wi = 0. The terminal region of constant viscosity is occurs due to the chains attaining their maximum stretch. thermal fluctuations are stronger than the hydrodynamic entanglement time) τd drag forces induced by the flow. This continues till the strain rate becomes −1 comparable to the inverse Rouse relaxation time τR . The behaviour of elongational viscosity in concentrated solutions and melts is different. as shown −1 ˙ τd . and is observed as an increase in the elongational viscosity in Equation (18). The viscosity is nearly same as the zero-shear rate viscosity. Most of these theoretical predictions have not been verified by experiments.20 Fig. the tubes (the pervaded schematically in Figure 12. This causes an increase in the viscosity. A semi-quantitative model for the behaviour in linear polymer melts can be interpreted in terms of the tube model or also called as the “standard molecular theory” [5]. which decreases the viscosity. mainly due to the difficulty in consistently measuring the elongational viscosity at very large strain rates and strains. and the chain remain in close to equilibrium microstructure.

1994) 7. Amsterdam. Larson. A compilation of recent works in melt rheology is given in Ref. Measurements.I. O. Handbook of Elementary Rheology (University of Wales. 1989) 2. Barnes. R. 1987) 3. J. Polymer Physics (Oxford University Press. H. J. R. Hassager. 39. J. Hutton.Volume 1: Fluid Mechanics. Dealy.A. Larson. J. (John Wiley. J.F. references to the sources containing details or other original references have been provided. Piau.F. Curtiss.C. Rheol. Rubinstein. J. R. Armstrong.M. The Structure and Rheology of Complex Fluids (Oxford University Press. Walters. M.M. Figures in this chapter The figures in this chapter have been schematically redrawn for educational purposes. H. 2nd edn.Volume 2: Kinetic Theory. Where possible. 2003) 4. 1987) 10.Polymer Rheology 21 Other reading An historical account of rheology in general is discussed in Ref. Bird. They may not bear direct comparisons with absolute values in reality. Dynamics of Polymeric Liquids . Dynamics of Polymeric Liquids . Armstrong. R. Amsterdam. C. Institute of NonNewtonian Fluid Mechanics. 2000) 5.B. Aberystwyth.B. New York.C. Rheology for Polymer Melt Processing (Elsevier. and Applications (Wiley-VCH. Walters. R. References 1. Structure and Rheology of Molten Polymers: From Structure to Flow Behaviour and Back Again (Hanser Publishers. R. 253 (1995) 9. R.M. and general rheology. (John Wiley. 1999) 8. Tanner. [10]. 2nd edn.H. Rheology: An Historical Perspective (Elsevier. An Introduction to Rheology (Elsevier. 1996) . Colby. K. K. Ref [7] contains an extensive literature survey of various aspects of polymer rheology. Agassant.W. Dealy.G. Hassager. O. 2006) 6. [11]. Macosko. Rheology: Principles. Barnes.A. C.G. New York. Bird.F. Munich. New York. R. 1998) 11.

You're Reading a Free Preview

/*********** DO NOT ALTER ANYTHING BELOW THIS LINE ! ************/ var s_code=s.t();if(s_code)document.write(s_code)//-->