Recoil (rheology)

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Recoil is a rheological phenomenon observed only in non-Newtonian fluids that is characterized by a moving fluid's ability to snap back to a previous position when external forces are removed. Recoil is a result of the fluid's elasticity and memory where the speed and acceleration by which the fluid moves depends on the molecular structure and the location to which it returns depends on the conformational entropy. This effect is observed in numerous non-Newtonian liquids to a small degree, but is prominent in some materials such as molten polymers.

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Memory

The degree to which a fluid will “remember” where it came from depends on the entropy. Viscoelastic properties in fluids cause them to snap back to entropically favorable conformations. [1] Recoil is observed when a favorable conformation is in the fluid's recent past. However, the fluid cannot fully return to its original position due to energy losses stemming from less than perfect elasticity.

Recoiling fluids display fading memory meaning the longer a fluid is elongated, the less it will recover. Recoil is related to characteristic time, an estimate of the order of magnitude of reaction for the system. Fluids that are described as recoiling generally have characteristic times on the order of a few seconds. [2] Although recoiling fluids usually recover relatively small distances, some molten polymers can recover back to 1/10 of the total elongation. [3] This property of polymers must be accounted for in polymer processing.

Demonstrations of Recoil

When a spinning rod is placed in a polymer solution, elastic forces generated by the rotation motion cause fluid to climb up the rod (a phenomenon known as the Weissenberg effect). If the torque being applied is immediately brought to a stop, the fluid recoils down the rod.

When a viscoelastic fluid being poured from a beaker is quickly cut with a pair of scissors, the fluid recoils back into the beaker. When fluid at rest in a circular tube is subjected to a pressure drop, a parabolic flow distribution is observed that pulls the liquid down the tube. Immediately after the pressure is alleviated, the fluid recoils backward in the tube and forms a more blunt flow profile. When Silly Putty is rapidly stretched and held at an elongated position for a short period of time, it springs back. However, if it is held at an elongated position for a longer period of time, there is very little recovery and no visible recoil. [4]

Related Research Articles

Rheology is the study of the flow of matter, primarily in a fluid state but also as "soft solids" or solids under conditions in which they respond with plastic flow rather than deforming elastically in response to an applied force. Rheology is the branch of physics that deals with the deformation and flow of materials, both solids and liquids.

<span class="mw-page-title-main">Gel</span> Highly viscous liquid exhibiting a kind of semi-solid behavior

A gel is a semi-solid that can have properties ranging from soft and weak to hard and tough. Gels are defined as a substantially dilute cross-linked system, which exhibits no flow when in the steady state, although the liquid phase may still diffuse through this system.

<span class="mw-page-title-main">Silly Putty</span> Toy putty (slime)

Silly Putty is a toy containing silicone polymers that have unusual physical properties. It can flow like a liquid, bounce, stretch, or break depending on the amount of physical stress to which it is subjected. It contains viscoelastic liquid silicones, a type of non-Newtonian fluid, which makes it act as a viscous liquid over a long time period but as an elastic solid over a short time period. It was originally created during research into potential rubber substitutes for use by the United States in World War II.

A non-Newtonian fluid is a fluid that does not follow Newton's law of viscosity, that is, it has variable viscosity dependent on stress. In particular, the viscosity of non-Newtonian fluids can change when subjected to force. Ketchup, for example, becomes runnier when shaken and is thus a non-Newtonian fluid. Many salt solutions and molten polymers are non-Newtonian fluids, as are many commonly found substances such as custard, toothpaste, starch suspensions, corn starch, paint, blood, melted butter, and shampoo.

The Deborah number (De) is a dimensionless number, often used in rheology to characterize the fluidity of materials under specific flow conditions. It quantifies the observation that given enough time even a solid-like material might flow, or a fluid-like material can act solid when it is deformed rapidly enough. Materials that have low relaxation times flow easily and as such show relatively rapid stress decay.

Dynamic mechanical analysis is a technique used to study and characterize materials. It is most useful for studying the viscoelastic behavior of polymers. A sinusoidal stress is applied and the strain in the material is measured, allowing one to determine the complex modulus. The temperature of the sample or the frequency of the stress are often varied, leading to variations in the complex modulus; this approach can be used to locate the glass transition temperature of the material, as well as to identify transitions corresponding to other molecular motions.

In physics and materials science, elasticity is the ability of a body to resist a distorting influence and to return to its original size and shape when that influence or force is removed. Solid objects will deform when adequate loads are applied to them; if the material is elastic, the object will return to its initial shape and size after removal. This is in contrast to plasticity, in which the object fails to do so and instead remains in its deformed state.

Hemorheology, also spelled haemorheology, or blood rheology, is the study of flow properties of blood and its elements of plasma and cells. Proper tissue perfusion can occur only when blood's rheological properties are within certain levels. Alterations of these properties play significant roles in disease processes. Blood viscosity is determined by plasma viscosity, hematocrit and mechanical properties of red blood cells. Red blood cells have unique mechanical behavior, which can be discussed under the terms erythrocyte deformability and erythrocyte aggregation. Because of that, blood behaves as a non-Newtonian fluid. As such, the viscosity of blood varies with shear rate. Blood becomes less viscous at high shear rates like those experienced with increased flow such as during exercise or in peak-systole. Therefore, blood is a shear-thinning fluid. Contrarily, blood viscosity increases when shear rate goes down with increased vessel diameters or with low flow, such as downstream from an obstruction or in diastole. Blood viscosity also increases with increases in red cell aggregability.

In materials science and continuum mechanics, viscoelasticity is the property of materials that exhibit both viscous and elastic characteristics when undergoing deformation. Viscous materials, like water, resist shear flow and strain linearly with time when a stress is applied. Elastic materials strain when stretched and immediately return to their original state once the stress is removed.

<span class="mw-page-title-main">Rheometer</span> Scientific instrument used to measure fluid flow (rheology)

A rheometer is a laboratory device used to measure the way in which a viscous fluid flows in response to applied forces. It is used for those fluids which cannot be defined by a single value of viscosity and therefore require more parameters to be set and measured than is the case for a viscometer. It measures the rheology of the fluid.

<span class="mw-page-title-main">Shear thinning</span> Non-Newtonian fluid behavior

In rheology, shear thinning is the non-Newtonian behavior of fluids whose viscosity decreases under shear strain. It is sometimes considered synonymous for pseudo-plastic behaviour, and is usually defined as excluding time-dependent effects, such as thixotropy.

<span class="mw-page-title-main">Manfred Wagner</span> German chemical engineer

Manfred Hermann Wagner is the author of Wagner model and the molecular stress function theory for polymer rheology. He is a Professor for Polymer engineering and Polymer physics at the Technical University of Berlin.

Rubber elasticity refers to a property of crosslinked rubber: it can be stretched by up to a factor of 10 from its original length and, when released, returns very nearly to its original length. This can be repeated many times with no apparent degradation to the rubber. Rubber is a member of a larger class of materials called elastomers and it is difficult to overestimate their economic and technological importance. Elastomers have played a key role in the development of new technologies in the 20th century and make a substantial contribution to the global economy. Rubber elasticity is produced by several complex molecular processes and its explanation requires a knowledge of advanced mathematics, chemistry and statistical physics, particularly the concept of entropy. Entropy may be thought of as a measure of the thermal energy that is stored in a molecule. Common rubbers, such as polybutadiene and polyisoprene, are produced by a process called polymerization. Very long molecules (polymers) are built up sequentially by adding short molecular backbone units through chemical reactions. A rubber polymer follows a random, zigzag path in three dimensions, intermingling with many other rubber molecules. An elastomer is created by the addition of a few percent of a cross linking molecule such as sulfur. When heated, the crosslinking molecule causes a reaction that chemically joins (bonds) two of the rubber molecules together at some point. Because the rubber molecules are so long, each one participates in many crosslinks with many other rubber molecules forming a continuous molecular network. As a rubber band is stretched, some of the network chains are forced to become straight and this causes a decrease in their entropy. It is this decrease in entropy that gives rise to the elastic force in the network chains.

<span class="mw-page-title-main">Time–temperature superposition</span>

The time–temperature superposition principle is a concept in polymer physics and in the physics of glass-forming liquids.

Constant viscosity elastic liquids, also known as Boger fluids are elastic fluids with constant viscosity. This creates an effect in the fluid where it flows like a liquid, yet behaves like an elastic solid when stretched out. Most elastic fluids exhibit shear thinning, because they are solutions containing polymers. But Boger fluids are exceptions since they are highly dilute solutions, so dilute that shear thinning caused by the polymers can be ignored. Boger fluids are made primarily by adding a small amount of polymer to a Newtonian fluid with a high viscosity, a typical solution being polyacrylamide mixed with corn syrup. It is a simple compound to synthesize but important to the study of rheology because elastic effects and shear effects can be clearly distinguished in experiments using Boger fluids. Without Boger fluids, it was difficult to determine if a non-Newtonian effect was caused by elasticity, shear thinning, or both; non-Newtonian flow caused by elasticity was rarely identifiable. Since Boger fluids can have constant viscosity, an experiment can be done where the results of the flow rates of a Boger liquid and a Newtonian liquid with the same viscosity can be compared, and the difference in the flow rates would show the change caused by the elasticity of the Boger liquid.

Rheological weldability (RW) of thermoplastics considers the materials flow characteristics in determining the weldability of the given material. The process of welding thermal plastics requires three general steps, first is surface preparation. The second step is the application of heat and pressure to create intimate contact between the components being joined and initiate inter-molecular diffusion across the joint and the third step is cooling. RW can be used to determine the effectiveness of the second step of the process for given materials.

A die in polymer processing is a metal restrictor or channel capable of providing a constant cross sectional profile to a stream of liquid polymer. This allows for continuous processing of shapes such as sheets, films, pipes, rods, and other more complex profiles. This is a continuous process, allowing for constant production, as opposed to a sequential (non-constant) process such as injection molding.

<span class="mw-page-title-main">Visco-elastic jets</span>

Visco-elastic jets are the jets of viscoelastic fluids, i.e. fluids that disobey Newton's law of Viscocity. A Viscoelastic fluid that returns to its original shape after the applied stress is released.

Capillary breakup rheometry is an experimental technique used to assess the extensional rheological response of low viscous fluids. Unlike most shear and extensional rheometers, this technique does not involve active stretch or measurement of stress or strain but exploits only surface tension to create a uniaxial extensional flow. Hence, although it is common practice to use the name rheometer, capillary breakup techniques should be better addressed to as indexers.

Mechanics of gelation describes processes relevant to sol-gel process.

References

  1. Rudin, Alfred, and Phillip Choi. The Elements of Polymer Science and Engineering. 3rd. Oxford: Academic Press, 2013. Print.
  2. Bird, R.B. Armstrong, R.C. and Hassager, O. Dynamics of Polymeric Liquids, Vol. 1, Fluid Mechanics, Wiley, New York (1977), p. 90-91.
  3. J. Meissner, Rheol. Acta, 10, (1971), p. 230-242.
  4. A.S. Lodge, Elastic Liquids, Academic Press, New York (1963), p. 236.