Viscosity
Viscosity (dynamic)  

A simulation of liquids with different viscosities. The liquid on the right has higher viscosity than the liquid on the left.  
Common symbols  η, μ 
Derivations from other quantities  μ = G·t 
The viscosity of a fluid is the measure of its resistance to gradual deformation by shear stress or tensile stress.^{[1]} For liquids, it corresponds to the informal concept of "thickness": for example, honey has a higher viscosity than water.^{[2]}
Viscosity is the property of a fluid which opposes the relative motion between two surfaces of the fluid that are moving at different velocities. In simple terms, viscosity means friction between the molecules of fluid. When the fluid is forced through a tube, the particles which compose the fluid generally move more quickly near the tube's axis and more slowly near its walls; therefore some stress (such as a pressure difference between the two ends of the tube) is needed to overcome the friction between particle layers to keep the fluid moving. For a given velocity pattern, the stress required is proportional to the fluid's viscosity.
A fluid that has no resistance to shear stress is known as an ideal or inviscid fluid. Zero viscosity is observed only at very low temperatures in superfluids. Otherwise, all fluids have positive viscosity and are technically said to be viscous or viscid. A fluid with a relatively high viscosity, such as pitch, may appear to be a solid.
Contents
Etymology[edit]
The word "viscosity" is derived from the Latin "viscum", meaning mistletoe and also a viscous glue made from mistletoe berries.^{[3]}
Definition[edit]
Dynamic (shear) viscosity [edit]
The dynamic viscosity of a fluid expresses its resistance to shearing flows, where adjacent layers move parallel to each other with different speeds. It can be defined through the idealized situation known as a Couette flow, where a layer of fluid is trapped between two horizontal plates, one fixed and one moving horizontally at constant speed . This fluid has to be homogeneous in the layer and at different shear stresses. (The plates are assumed to be very large so that one need not consider what happens near their edges.)
If the speed of the top plate is low enough, the fluid particles will move parallel to it, and their speed will vary linearly from zero at the bottom to u at the top. Each layer of fluid will move faster than the one just below it, and friction between them will give rise to a force resisting their relative motion. In particular, the fluid will apply on the top plate a force in the direction opposite to its motion, and an equal but opposite one to the bottom plate. An external force is therefore required in order to keep the top plate moving at constant speed.
The magnitude F of this force is found to be proportional to the speed u and the area A of each plate, and inversely proportional to their separation y:
The proportionality factor μ in this formula is the viscosity (specifically, the dynamic viscosity) of the fluid, with units of (pascalsecond).
The ratio u/y is called the rate of shear deformation or shear velocity, and is the derivative of the fluid speed in the direction perpendicular to the plates (see illustrations to the right). Isaac Newton expressed the viscous forces by the differential equation
where τ = F/A, and ∂u/∂y is the local shear velocity. This formula assumes that the flow is moving along parallel lines to xaxis. Furthermore, it assumes that the yaxis, perpendicular to the flow, points in the direction of maximum shear velocity. This equation can be used where the velocity does not vary linearly with y, such as in fluid flowing through a pipe. This equation is called the defining equation for shear viscosity. The viscosity is not a material constant, but a material property that depends on physical properties like temperature. The variation of the dynamic viscosity μ at a given temperature can be evaluated on the basis of the dynamic viscosity at room temperature () by the equation: ^{[4]}
The functional relationship between viscosity and other physical properties is described by mathematical viscosity models called constitutive equations which are usually more complex than the defining equation for viscosity. There exist many viscosity models, and based on type of developmentreasoning, some viscosity models are selected and presented in the article Viscosity models for mixtures.
Use of the Greek letter mu (μ) for the dynamic viscosity is common among mechanical and chemical engineers, as well as physicists.^{[5]}^{[6]}^{[7]} However, the Greek letter eta (η) is also used by chemists, physicists, and the IUPAC.^{[8]}
Kinematic viscosity[edit]
The kinematic viscosity (also called "momentum diffusivity") is the ratio of the dynamic viscosity μ to the density of the fluid ρ. It is usually denoted by the Greek letter nu (ν) and has units .
A convenient concept when analyzing the Reynolds number, which expresses the ratio of the inertial forces to the viscous forces, is:
where D is a diameter in the system, and V is the velocity of the fluid with respect to the object (m/s).
Bulk viscosity[edit]
When a compressible fluid is compressed or expanded evenly, without shear, it may still exhibit a form of internal friction that resists its flow. These forces are related to the rate of compression or expansion by a factor called the volume viscosity, bulk viscosity or second viscosity.
The bulk viscosity is important only when the fluid is being rapidly compressed or expanded, such as in sound and shock waves. Bulk viscosity explains the loss of energy in those waves, as described by Stokes' law of sound attenuation.
Viscosity tensor[edit]
In general, the stresses within a flow can be attributed partly to the deformation of the material from some rest state (elastic stress), and partly to the rate of change of the deformation over time (viscous stress). In a fluid, by definition, the elastic stress includes only the hydrostatic pressure.
In very general terms, the fluid's viscosity is the relation between the strain rate and the viscous stress. In the Newtonian fluid model, the relationship is by definition a linear map, described by a viscosity tensor that, multiplied by the strain rate tensor (which is the gradient of the flow's velocity), gives the viscous stress tensor.
The viscosity tensor has nine independent degrees of freedom in general. For isotropic Newtonian fluids, these can be reduced to two independent parameters. The most usual decomposition yields the dynamic viscosity μ and the bulk viscosity σ.
Newtonian and nonNewtonian fluids[edit]
Newton's law of viscosity is a constitutive equation (like Hooke's law, Fick's law, and Ohm's law): it is not a fundamental law of nature but an approximation that holds in some materials and fails in others.
A fluid that behaves according to Newton's law, with a viscosity μ that is independent of the stress, is said to be Newtonian. Gases, water, and many common liquids can be considered Newtonian in ordinary conditions and contexts. There are many nonNewtonian fluids that significantly deviate from that law in some way or other. For example:
 Shearthickening liquids, whose viscosity increases with the rate of shear strain.
 Shearthinning liquids, whose viscosity decreases with the rate of shear strain.
 Thixotropic liquids, that become less viscous over time when shaken, agitated, or otherwise stressed.
 Rheopectic (dilatant) liquids, that become more viscous over time when shaken, agitated, or otherwise stressed.
 Bingham plastics that behave as a solid at low stresses but flow as a viscous fluid at high stresses.
Shearthinning liquids are very commonly, but misleadingly, described as thixotropic.
Even for a Newtonian fluid, the viscosity usually depends on its composition and temperature. For gases and other compressible fluids, it depends on temperature and varies very slowly with pressure.
The viscosity of some fluids may depend on other factors. A magnetorheological fluid, for example, becomes thicker when subjected to a magnetic field, possibly to the point of behaving like a solid.
In solids[edit]
The viscous forces that arise during fluid flow must not be confused with the elastic forces that arise in a solid in response to shear, compression or extension stresses. While in the latter the stress is proportional to the amount of shear deformation, in a fluid it is proportional to the rate of deformation over time. (For this reason, Maxwell used the term fugitive elasticity for fluid viscosity.)
However, many liquids (including water) will briefly react like elastic solids when subjected to sudden stress. Conversely, many "solids" (even granite) will flow like liquids, albeit very slowly, even under arbitrarily small stress.^{[9]} Such materials are therefore best described as possessing both elasticity (reaction to deformation) and viscosity (reaction to rate of deformation); that is, being viscoelastic.
Indeed, some authors have claimed that amorphous solids, such as glass and many polymers, are actually liquids with a very high viscosity (greater than 10^{12} Pa·s). ^{[10]} However, other authors dispute this hypothesis, claiming instead that there is some threshold for the stress, below which most solids will not flow at all,^{[11]} and that alleged instances of glass flow in window panes of old buildings are due to the crude manufacturing process of older eras rather than to the viscosity of glass.^{[12]}
Viscoelastic solids may exhibit both shear viscosity and bulk viscosity. The extensional viscosity is a linear combination of the shear and bulk viscosities that describes the reaction of a solid elastic material to elongation. It is widely used for characterizing polymers.
In geology, earth materials that exhibit viscous deformation at least three orders of magnitude greater than their elastic deformation are sometimes called rheids.^{[13]}
Measurement[edit]
Viscosity is measured with various types of viscometers and rheometers. A rheometer is used for those fluids that 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. Close temperature control of the fluid is essential to acquire accurate measurements, particularly in materials like lubricants, whose viscosity can double with a change of only 5 °C.
For some fluids, the viscosity is constant over a wide range of shear rates (Newtonian fluids). The fluids without a constant viscosity (nonNewtonian fluids) cannot be described by a single number. NonNewtonian fluids exhibit a variety of different correlations between shear stress and shear rate.
One of the most common instruments for measuring kinematic viscosity is the glass capillary viscometer.
In coating industries, viscosity may be measured with a cup in which the efflux time is measured. There are several sorts of cup – such as the Zahn cup and the Ford viscosity cup – with the usage of each type varying mainly according to the industry. The efflux time can also be converted to kinematic viscosities (centistokes, cSt) through the conversion equations.^{[14]}
Also used in coatings, a Stormer viscometer uses loadbased rotation in order to determine viscosity. The viscosity is reported in Krebs units (KU), which are unique to Stormer viscometers.
Vibrating viscometers can also be used to measure viscosity. Resonant, or vibrational viscometers work by creating shear waves within the liquid. In this method, the sensor is submerged in the fluid and is made to resonate at a specific frequency. As the surface of the sensor shears through the liquid, energy is lost due to its viscosity. This dissipated energy is then measured and converted into a viscosity reading. A higher viscosity causes a greater loss of energy.^{[citation needed]}
Extensional viscosity can be measured with various rheometers that apply extensional stress.
Volume viscosity can be measured with an acoustic rheometer.
Apparent viscosity is a calculation derived from tests performed on drilling fluid used in oil or gas well development. These calculations and tests help engineers develop and maintain the properties of the drilling fluid to the specifications required.
Units[edit]
Dynamic viscosity, μ[edit]
Both the physical unit of dynamic viscosity in SI units, the poiseuille (Pl), and cgs units, the poise (P), are named after Jean Léonard Marie Poiseuille. The poiseuille, which is rarely used, is equivalent to the pascal second (Pa·s), or (N·s)/m^{2}, or kg/(m·s). If a fluid is placed between two plates with distance one meter, and one plate is pushed sideways with a shear stress of one pascal, and it moves at x meters per second, then it has viscosity of 1/x pascal seconds. For example, water at 20 °C has a viscosity of 1.002 mPa·s, while a typical motor oil could have a viscosity of about 250 mPa·s.^{[15]} The units used in practice are either Pa·s and its submultiples or the cgs poise referred to below, and its submultiples.
The cgs physical unit for dynamic viscosity, the poise^{[16]} (P), is also named after Jean Poiseuille. It is more commonly expressed, particularly in ASTM standards, as centipoise (cP) since the latter is equal to the SI multiple millipascal seconds (mPa·s). For example, water at 20 °C has a viscosity of 1.002 mPa·s = 1.002 cP.
 1 Pl = 1 Pa·s
 1 P = 1 dPa·s = 0.1 Pa·s = 0.1 kg·m^{−1}·s^{−1}
 1 cP = 1 mPa·s = 0.001 Pa·s = 0.001 N·s·m^{−2} = 0.001 kg·m^{−1}·s^{−1}.
Kinematic viscosity, ν[edit]
The SI unit of kinematic viscosity is m^{2}/s.
The cgs physical unit for kinematic viscosity is the stokes (St), named after Sir George Gabriel Stokes.^{[17]} It is sometimes expressed in terms of centistokes (cSt). In U.S. usage, stoke is sometimes used as the singular form.
 1 St = 1 cm^{2}·s^{−1} = 10^{−4} m^{2}·s^{−1}.
 1 cSt = 1 mm^{2}·s^{−1} = 10^{−6 }m^{2}·s^{−1}.
Water at 20 °C has a kinematic viscosity of about 10^{−6 }m^{2}·s^{−1} or 1 cSt.
The kinematic viscosity is sometimes referred to as diffusivity of momentum, because it is analogous to diffusivity of heat and diffusivity of mass. It is therefore used in dimensionless numbers which compare the ratio of the diffusivities.
Fluidity[edit]
The reciprocal of viscosity is fluidity, usually symbolized by φ = 1/μ or F = 1/μ, depending on the convention used, measured in reciprocal poise (P^{−1}, or cm·s·g^{−1}), sometimes called the rhe. Fluidity is seldom used in engineering practice.
The concept of fluidity can be used to determine the viscosity of an ideal solution. For two components A and B, the fluidity when A and B are mixed is
which is only slightly simpler than the equivalent equation in terms of viscosity:
where χ_{A} and χ_{B} are the mole fractions of components A and B respectively, and μ_{A} and μ_{B} are the components' pure viscosities.
Nonstandard units[edit]
The reyn is a British unit of dynamic viscosity.
Viscosity index is a measure for the change of viscosity with temperature. It is used in the automotive industry to characterise lubricating oil.
At one time the petroleum industry relied on measuring kinematic viscosity by means of the Saybolt viscometer, and expressing kinematic viscosity in units of Saybolt universal seconds (SUS).^{[18]} Other abbreviations such as SSU (Saybolt seconds universal) or SUV (Saybolt universal viscosity) are sometimes used. Kinematic viscosity in centistokes can be converted from SUS according to the arithmetic and the reference table provided in ASTM D 2161.^{[19]}
Molecular origins[edit]
In general, the viscosity of a system depends in detail on how the molecules constituting the system interact. There are no simple but correct expressions for the viscosity of a fluid. The simplest exact expressions are the Green–Kubo relations for the linear shear viscosity or the transient time correlation function expressions derived by Evans and Morriss in 1985.^{[21]} Although these expressions are each exact, calculating the viscosity of a dense fluid using these relations currently requires the use of molecular dynamics computer simulations. On the other hand, much more progress can be made for a dilute gas. Even elementary assumptions about how gas molecules move and interact lead to a basic understanding of the molecular origins of viscosity. More sophisticated treatments can be constructed by systematically coarsegraining the equations of motion of the gas molecules. An example of such a treatment is Chapman–Enskog theory, which derives expressions for the viscosity of a dilute gas from the Boltzmann equation.^{[22]}
Momentum transport in gases is generally mediated by discrete molecular collisions, and in liquids by attractive forces which bind molecules close together.^{[23]} Because of this, the dynamic viscosities of liquids are typically several orders of magnitude higher than dynamic viscosities of gases.
Gases[edit]
Viscosity in gases arises principally from the molecular diffusion that transports momentum between layers of flow. An elementary calculation for a dilute gas at temperature and density gives
where is the Boltzmann constant, the molecular mass, and a numerical constant on the order of . The quantity , the mean free path, measures the average distance a molecule travels between collisions. Even without a priori knowledge of , this expression has interesting implications. In particular, since is typically inversely proportional to density and increases with temperature, itself should increase with temperature and be independent of density. In fact, both of these predictions persist in more sophisticated treatments, and accurately describe experimental observations. Note that this behavior runs counter to common intuition regarding liquids, for which viscosity typically decreases with temperature.^{[23]}^{[24]}
Elementary calculation of viscosity for a dilute gas^{[25]} Consider a dilute gas moving parallel to the axis with velocity that depends only on the coordinate. To simplify the discussion, the gas is assumed to have uniform temperature and density.
Under these assumptions, the velocity of a molecule passing through is equal to whatever velocity that molecule had when its mean free path began. Because is typically small compared with macroscopic scales, the average velocity of such a molecule has the form
 ,
where is a numerical constant on the order of . (Some authors estimate ;^{[23]}^{[24]} on the other hand, a more careful calculation for rigid elastic spheres gives .) Now, because half the molecules on either side are moving towards , and doing so on average with half the average moleculer speed , the momentum flux from either side is
The net momentum flux at is the difference of the two:
According to the definition of viscosity, this momentum flux should be equal to , which leads to
For rigid elastic spheres of diameter , can be computed, giving
In this case is independent of temperature, so . For more complicated molecular models, however, depends on temperature in a nontrivial way, and simple kinetic arguments as used here are inadequate. More fundamentally, the notion of a mean free path becomes imprecise for particles that interact over a finite range, which limits the usefulness of the concept for describing realworld gases.^{[26]}
Chapman–Enskog theory[edit]
A technique developed by Sydney Chapman and David Enskog in the early 1900s allows a more refined calculation of .^{[22]} It is based on the Boltzmann equation, which provides a systematic statistical description of a dilute gas in terms of intermolecular interactions.^{[27]} As such, their technique allows accurate calculation of for more realistic molecular models, such as those incorporating intermolecular attraction rather than just hardcore repulsion.
It turns out that a more realistic modeling of interactions is essential for accurate prediction of the temperature dependence of , which experiments show increases more rapidly than the trend predicted for rigid elastic spheres.^{[23]} Indeed, the Chapman–Enskog analysis shows that the predicted temperature dependence can be tuned by varying the parameters in various molecular models. A simple example is the Sutherland model,^{[28]} which describes rigid elastic spheres with weak mutual attraction. In such a case, the attractive force can be treated perturbatively, which leads to a particularly simple expression for :
where is independent of temperature, being determined only by the parameters of the intermolecular attraction. To connect with experiment, it is convenient to rewrite as
where is the viscosity at temperature . If is known from experiments at and at least one other temperature, then can be calculated. It turns out that expressions for obtained in this way are accurate for a number of gases over a sizable range of temperatures. On the other hand, Chapman and Cowling^{[22]} argue that this success does not imply that molecules actually interact according to the Sutherland model. Rather, they interpret the prediction for as a simple interpolation which is valid for some gases over fixed ranges of temperature, but otherwise does not provide a picture of intermolecular interactions which is fundamentally correct and general. Slightly more sophisticated models, such as the Lennard–Jones potential, may provide a better picture, but only at the cost of a more opaque dependence on temperature. In some systems the assumption of spherical symmetry must be abandoned as well, as is the case for vapors with highly polar molecules like H_{2}O.^{[29]}^{[30]}
Liquids[edit]
In contrast with gases, there is no simple yet accurate picture for the molecular origins of viscosity in liquids.
At the simplest level of description, the relative motion of adjacent layers in a liquid is opposed primarily by attractive molecular forces acting across the layer boundary. In this picture, one (correctly) expects viscosity to decrease with temperature. This is because increasing temperature increases the random thermal motion of the molecules, which makes it easier for them to overcome their attractive interactions.^{[31]}
Building on this visualization, a simple theory can be constructed in analogy with the discrete structure of a solid: groups of molecules in a liquid are visualized as forming "cages" which surround and enclose single molecules.^{[32]} These cages can be occupied or unoccupied, and stronger molecular attraction corresponds to stronger cages. Due to random thermal motion, a molecule "hops" between cages at a rate which varies inversely with the strength of molecular attractions. In equilibrium these "hops" are not biased in any direction. On the other hand, in order for two adjacent layers to move relative to each other, the "hops" must be biased in the direction of the relative motion. The force required to sustain this directed motion can be estimated for a given shear rate, leading to

(1)
where is the Avogadro constant, is the Planck constant, is the volume of a mole of liquid, and is the boiling temperature. This result has the same form as the widespread and accurate empirical relation

(2)
where and are constants fit from data.^{[33]}^{[34]} One the other hand, several authors express caution with respect to this model. Errors as large as 30% can be encountered using equation (1), compared with fitting equation (2) to experimental data.^{[35]} More fundamentally, the physical assumptions underlying equation (1) have been extensively criticized.^{[36]} It has also been argued that the exponential dependence in equation (1) does not necessarily describe experimental observations more accurately than simpler, nonexponential expressions.^{[37]}^{[38]}
In light of these shortcomings, the development of a less adhoc model is a matter of practical interest. Foregoing simplicity in favor of precision, it is possible to write rigorous expressions for viscosity starting from the fundamental equations of motion for molecules. A classic example of this approach is IrvingKirkwood theory.^{[39]} On the other hand, such expressions are given as averages over multiparticle correlation functions and are therefore difficult to apply in practice.
In general, empirically derived expressions (based on existing viscosity measurements) appear to be the only consistently reliable means of calculating viscosity in liquids.^{[40]}
Selected substances[edit]
Air[edit]
The viscosity of air depends mostly on the temperature. At 15 °C, the viscosity of air is ×10^{−5} kg/(m·s), 18.1 μPa·s or 1.81×10^{−5} Pa·s. The kinematic viscosity at 15 °C is 1.81×10^{−5} m^{2}/s or 14.8 cSt. At 25 °C, the viscosity is 18.6 μPa·s and the kinematic viscosity 15.7 cSt. 1.48
Water[edit]
The dynamic viscosity of water is ×10^{−4} Pa·s or 8.90×10^{−3} dyn·s/cm^{2} or 0.890 cP at about 25 °C. 8.90
As a function of temperature T (in kelvins): μ = A × 10^{B/(T − C)}, where A = ×10^{−5} Pa·s, 2.414B = 247.8 K, and C = 140 K.^{[citation needed]}
The dynamic viscosity of liquid water at different temperatures up to the normal boiling point is listed below.
Temperature (°C)  Viscosity (mPa·s) 

10  1.308 
20  1.002 
30  0.7978 
40  0.6531 
50  0.5471 
60  0.4658 
70  0.4044 
80  0.3550 
90  0.3150 
100  0.2822 
Other substances[edit]
Some dynamic viscosities of Newtonian fluids are listed below:
Gas  at 0 °C (273 K)  at 27 °C (300 K)^{[41]} 

air  17.4  18.6 
hydrogen  8.4  9.0 
helium  20.0  
argon  22.9  
xenon  21.2  23.2 
carbon dioxide  15.0  
methane  11.2  
ethane  9.5 
Fluid  Viscosity (Pa·s)  Viscosity (cP) 

blood (37 °C)^{[10]}  ×10^{−3} – 3×10^{−3} 4  3–4 
honey  2–10^{[42]}  2000–000 10 
molasses  5–10  5000–000 10 
molten glass  10–1000  000– 10000000 1 
chocolate syrup  10–25  000– 10000 25 
molten chocolate^{[a]}  45–130^{[43]}  000– 45000 130 
ketchup^{[a]}  50–100  000– 50000 100 
lard  ≈ 100  ≈ 000 100 
peanut butter^{[a]}  ≈ 250  ≈ 000 250 
shortening^{[a]}  ≈ 250  ≈ 000 250 
Liquid  Viscosity (Pa·s)  Viscosity (cP) 

acetone^{[41]}  ×10^{−4} 3.06  0.306 
benzene^{[41]}  ×10^{−4} 6.04  0.604 
castor oil^{[41]}  0.985  985 
corn syrup^{[41]}  1.3806  1380.6 
ethanol^{[41]}  ×10^{−3} 1.074  1.074 
ethylene glycol  ×10^{−2} 1.61  16.1 
glycerol (at 20 °C)^{[44]}  1.2  1200 
HFO380  2.022  2022 
mercury^{[41]}  ×10^{−3} 1.526  1.526 
methanol^{[41]}  ×10^{−4} 5.44  0.544 
motor oil SAE 10 (20 °C)^{[45]}  0.065  65 
motor oil SAE 40 (20 °C)^{[45]}  0.319  319 
nitrobenzene^{[41]}  ×10^{−3} 1.863  1.863 
liquid nitrogen (−196 °C)  ×10^{−4} 1.58  0.158 
propanol^{[41]}  ×10^{−3} 1.945  1.945 
olive oil  0.081  81 
pitch  ×10^{8} 2.3  ×10^{11} 2.30 
sulfuric acid^{[41]}  ×10^{−2} 2.42  24.2 
water  ×10^{−4} 8.94  0.894 
Solid  Viscosity (Pa·s)  Temperature (°C) 

granite^{[9]}  ×10^{19}  3×10^{19} 6  25 
asthenosphere^{[46]}  ×10^{19} 7.0  900 
upper mantle^{[46]}  ×10^{20} – 7×10^{21} 1  1300–3000 
lower mantle  ×10^{21} – 1×10^{21} 2  3000–4000 
 ^ ^{a} ^{b} ^{c} ^{d} These materials are highly nonNewtonian.
Blends of liquids[edit]
The viscosity of the blend of two or more liquids can be estimated using the Refutas equation.^{[47]}^{[48]} The calculation is carried out in three steps.
The first step is to calculate the viscosity blending number (VBN) (also called the viscosity blending index) of each component of the blend:
 (1)
where ν is the kinematic viscosity in centistokes (cSt). It is important that the kinematic viscosity of each component of the blend be obtained at the same temperature.
The next step is to calculate the VBN of the blend, using this equation:
 (2)
where x_{X} is the mass fraction of each component of the blend.
Once the viscosity blending number of a blend has been calculated using equation (2), the final step is to determine the kinematic viscosity of the blend by solving equation (1) for ν:
 (3)
where VBN_{Blend} is the viscosity blending number of the blend.
alternatively use the more accurate LedererRoegiers equation [1]
 is based on the difference in intermolecular cohesion energies between the liquids
 =dynamic viscosity
 =mole fraction of particle species
Slurry[edit]
The term slurry describes mixtures of a liquid and solid particles that retain some fluidity. The viscosity of slurry can be described as relative to the viscosity of the liquid phase:
where μ_{s} and μ_{l} are respectively the dynamic viscosity of the slurry and liquid (Pa·s), and μ_{r} is the relative viscosity (dimensionless).
Depending on the size and concentration of the solid particles, several models exist that describe the relative viscosity as a function of volume fraction φ of solid particles.
In the case of extremely low concentrations of fine particles, Einstein's equation^{[49]} may be used:
In the case of higher concentrations, a modified equation was proposed by Guth and Simha,^{[50]} which takes into account interaction between the solid particles:
Further modification of this equation was proposed by Thomas^{[51]} from the fitting of empirical data:
where A = 73 and 0.002B = 16.6.
In the case of high shear stress (above 1 kPa), another empirical equation was proposed by Kitano et al. for polymer melts:^{[52]}
where A = 0.68 for smooth spherical particles.
Nanofluids[edit]
Nanofluid is a novel class of fluid, which is developed by dispersing nanosized particles in base fluid.^{[53]}
Einstein model
Einstein derived the applicable first theoretical formula for the estimation of viscosity values of composites or mixtures in 1906. This model developed while assuming linear viscous fluid including suspensions of rigid and spherical particles. Einstein’s model is valid for very low volume fraction .^{[49]}
Brinkman model
Brinkman modified Einstein’s model for used with average particle volume fraction up to 4%^{[54]}
Batchelor model
Batchelor reformed Einstein's theoretical model by presenting Brownian motion effect.^{[55]}
Wang et al. model
Wang et al. found a model to predict viscosity of nanofluid as follows.^{[56]}
Masoumi et al. model
Masoumi et al. suggested a new viscosity correlation by considering Brownian motion of nanoparticle in nanofluid.^{[57]}
Udawattha et al. model
Udawattha et al. modified the Masoumi et al. model. The developed model valid for suspension containing microsize particles.^{[58]}
where
 is the viscosity of the sample, in [Pa·s]
 is nanofluid
 is basefluid
 is particle
 is volume fraction
 is density of the sample, in [kg·m^{−3}]
 is distance between two particles
 is Brownian motion of particle
 is the Boltzmann constant
 is Temperature of the sample, in [K]
 is diameter of a particle
 is nanolayer thickness (1 nm)
 is radius of a particle
Amorphous materials[edit]
Viscous flow in amorphous materials (e.g. in glasses and melts)^{[60]}^{[61]}^{[62]} is a thermally activated process:
where Q is activation energy, T is temperature, R is the molar gas constant and A is approximately a constant.
The viscous flow in amorphous materials is characterized by a deviation from the Arrheniustype behavior: Q changes from a high value Q_{H} at low temperatures (in the glassy state) to a low value Q_{L} at high temperatures (in the liquid state). Depending on this change, amorphous materials are classified as either
 strong when: Q_{H} − Q_{L} < Q_{L} or
 fragile when: Q_{H} − Q_{L} ≥ Q_{L}.
The fragility of amorphous materials is numerically characterized by Doremus' fragility ratio:
and strong materials have R_{D} < 2 whereas fragile materials have R_{D} ≥ 2.
The viscosity of amorphous materials is quite exactly described by a twoexponential equation:
with constants A_{1}, A_{2}, B, C and D related to thermodynamic parameters of joining bonds of an amorphous material.
Not very far from the glass transition temperature, T_{g}, this equation can be approximated by a Vogel–Fulcher–Tammann (VFT) equation.
If the temperature is significantly lower than the glass transition temperature, T ≪ T_{g}, then the twoexponential equation simplifies to an Arrheniustype equation:
with
where H_{d} is the enthalpy of formation of broken bonds (termed configurons^{[63]}) and H_{m} is the enthalpy of their motion.
When the temperature is less than the glass transition temperature, T < T_{g}, the activation energy of viscosity is high because the amorphous materials are in the glassy state and most of their joining bonds are intact.
If the temperature is much higher than the glass transition temperature, T ≫ T_{g}, the twoexponential equation also simplifies to an Arrheniustype equation:
with
When the temperature is higher than the glass transition temperature, T > T_{g}, the activation energy of viscosity is low because amorphous materials are melted and have most of their joining bonds broken, which facilitates flow.
Eddy viscosity[edit]
In the study of turbulence in fluids, a common practical strategy for calculation is to ignore the smallscale vortices (or eddies) in the motion and to calculate a largescale motion with an eddy viscosity that characterizes the transport and dissipation of energy in the smallerscale flow (see large eddy simulation). Values of eddy viscosity used in modeling ocean circulation may be from ×10^{4} to 5×10^{6} Pa·s depending upon the resolution of the numerical grid. 1
See also[edit]
 Dashpot
 Deborah number
 Dilatant
 Herschel–Bulkley fluid
 Hyperviscosity syndrome
 Intrinsic viscosity
 Inviscid flow
 Joback method (estimation of the liquid viscosity from molecular structure)
 Kaye effect
 Microviscosity
 Morton number
 Orders of magnitude (viscosity)
 Quasisolid
 Rheology
 Stokes flow
 Superfluid helium4
 Trouton's ratio
 Viscoplasticity
 Viscosity models for mixtures
References[edit]
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Further reading[edit]
 Hatschek, Emil (1928). The Viscosity of Liquids. New York: Van Nostrand. OCLC 53438464.
 Massey, B. S.; WardSmith, A. J. (2011). Mechanics of Fluids (9th ed.). London & New York: Spon Press. ISBN 9780415602594. OCLC 690084654.
External links[edit]
Look up viscosity in Wiktionary, the free dictionary. 
Wikisource has the text of The New Student's Reference Work article Viscosity of Liquids. 
 Fluid properties  high accuracy calculation of viscosity for frequently encountered pure liquids and gases
 Gas viscosity calculator as function of temperature
 Air viscosity calculator as function of temperature and pressure
 Fluid Characteristics Chart  a table of viscosities and vapor pressures for various fluids
 Gas Dynamics Toolbox  calculate coefficient of viscosity for mixtures of gases
 Glass Viscosity Measurement  viscosity measurement, viscosity units and fixpoints, glass viscosity calculation
 Kinematic Viscosity  conversion between kinematic and dynamic viscosity
 Physical Characteristics of Water  a table of water viscosity as a function of temperature
 Vogel–Tammann–Fulcher Equation Parameters
 Calculation of temperaturedependent dynamic viscosities for some common components
 "Test Procedures for Testing Highway and Nonroad Engines and Omnibus Technical Amendments"  United States Environmental Protection Agency
 Artificial viscosity
 Viscosity of Air, Dynamic and Kinematic, Engineers Edge