Capillary tube Etched rings British Standard U-tube viscometer Capillary tube Capillary tube Etched rings Glass strengthening bridge Kinematic viscometers for transparent fluids for opaq
Trang 1υ = πr 4 glt / 8LV = k(t 2 − t 1 ) (2.15)where:
υ is the kinematic viscosity [m2/s];
r is the capillary radius [m];
l is the mean hydrostatic head [m];
g is the earth acceleration [m/s2];
L is the capillary length [m];
V is the flow volume of the fluid [m3];
t is the flow time through the capillary, t = (t 2 − t 1 ), [s];
k is the capillary constant which has to be determined experimentally by applying
a reference fluid with known viscosity, e.g by applying freshly distilled water.The capillary constant is usually given by the manufacturer of the viscometer
Capillary tube
Etched
rings
British Standard U-tube viscometer
Capillary tube Capillary
tube
Etched rings
Glass strengthening bridge
Kinematic viscometers
for transparent fluids for opaquefluids
FIGURE 2.10 Typical capillary viscometers (adapted from [23])
In order to measure the viscosity of the fluid by one of the viscometers shown in Figure 2.10,the container is filled with oil between the etched lines The measurement is then made bytiming the period required for the oil meniscus to flow from the first to the second timingmark This is measured with an accuracy to within 0.1 [s]
Kinematic viscosity can also be measured by so called ‘short tube’ viscometers In theliterature they are also known as efflux viscometers As in the previously describedviscometers, viscosity is determined by measuring the time necessary for a given volume offluid to discharge under gravity through a short tube orifice in the base of the instrument.The most commonly used viscometers are Redwood, Saybolt and Engler The operationprinciple of these viscometers is the same, and they only differ by the orifice dimensions andthe volume of fluid discharged Redwood viscometers are used in the United Kingdom,Saybolt in Europe and Engler mainly in former Eastern Europe The viscosities measured bythese viscometers are quoted in terms of the time necessary for the discharge of a certainvolume of fluid Hence the viscosity is sometimes found as being quoted in Redwood and
Trang 2Saybolt seconds The viscosity measured on Engler viscometers is quoted in Engler degrees,which is the time for the fluid to discharge divided by the discharge time of the same volume
of water at the same temperature Redwood and Saybolt seconds and Engler degrees caneasily be converted into centistokes as shown in Figure 2.11 These particular types ofviscometers, are gradually becoming obsolete, since they do not easily provide calculableviscosity A typical short tube viscometer is shown in Figure 2.12
In order to extend the range of kinematic, Saybolt Universal, Redwood No 1 and Englerviscosity scales only (Figure 2.11), a simple operation is performed The viscosities on thesescales which correspond to the viscosity between 100 and 1000 [cS] on the kinematic scale aremultiplied by a factor of 10 and this gives the required extension For example:
4000 [cS] = 400 [cS]×10≈1850 [SUS]×10 = 18500 [SUS]≈51 [Engler]×10 = 510 [Engler]
2 2.5 3 3.5 4 4.5 5 6 7 8 10
15 20 25 30 35 40 50 60 70 80 90 100
150 200 250 300 350 400 500 600 700 800
1 000
2 2.5 3 3.5 4 4.5 5 6 7 8 10
15 20 25 30 35 40 50 60 70 80 90 100
150 200 250 300 350 400 500 600 700 800
1 000
100
150 200 250 300 350 400 450 600 700 800 900
60 70 80 90
100
150 200 250 300 350 400 450 600 700 800
60 70 80 90
2 2.5 3 3.5 4 4.5 5
6 7 8 9 10
15 20 25 30 35 40 50 60 70 80
1.9 1.7 1.6
1.5 1.4 1.3 1.2
25 30 35 40 50 60 70 80 90 100
150 200 250 300 350 400 450
30 35 40 45 60 70 80 90 100
150 200 250 300 350 400 100
in between The measurements are conducted by applying either a constant torque andmeasuring the changes in the speed of rotation or applying a constant speed and measuring
Trang 3the changes in the torque These viscometers give the ‘dynamic viscosity’ There are two
main types of these viscometers: rotating cylinder and cone-on-plate viscometers
Stopper
Capillary tube
Lubricant sample
Water bath
Overflow rim
FIGURE 2.12 Schematic diagram of a short tube viscometer
· Rotating Cylinder Viscometer
The rotating cylinder viscometer, also known as a ‘Couette viscometer’, consists of twoconcentric cylinders with an annular clearance filled with fluid as shown in Figure 2.13 Theinside cylinder is stationary and the outside cylinder rotates at constant velocity The forcenecessary to shear the fluid between the cylinders is measured The velocity of the cylindercan be varied so that the changes in viscosity of the fluid with shear rate can be assessed Careneeds to be taken with non-Newtonian fluids as these viscometers are calibrated forNewtonian fluids Different cylinders with a range of radial clearances are used for differentfluids For Newtonian fluids the dynamic viscosity can be estimated from the formula:
where:
η is the dynamic viscosity [Pas];
r b , r c are the radii of the inner and outer cylinders respectively [m];
M is the shear torque on the inner cylinder [Nm];
ω is the angular velocity [rad/s];
d is the immersion depth of the inner cylinder [m];
k is the viscometer constant, supplied usually by the manufacturer for each pair of
cylinders [m-3]
When motor oils are used in European and North American conditions, the oil viscositydata at -18°C is required in order to assess the ease with which the engine starts A speciallyadapted rotating cylinder viscometer, known in the literature as the ‘Cold CrankingSimulator’ (CCS), is used for this purpose (ASTM D2602) The schematic diagram of thisviscometer is shown in Figure 2.14
Trang 4Fluid sample
ω
r c
r b
Inner cylinder (stationary)
Outer cylinder (rotating)
FIGURE 2.13 Schematic diagram of a rotating cylinder viscometer
Overload clutch
Constant-power motor drive with tachometer
Coolant
(methanol)
in
Coolant out
Nylon block
Thermocouple
ω
Lubricant sample
Rotating cylinder
Stationary cylinder
FIGURE 2.14 Schematic diagram of a cold cranking simulator
The inner cylinder is rotated at constant power in the cooled lubricant sample of volumeabout 5 [ml] The viscosity of the oil sample tested is assessed by comparing the rotationalspeed of the test oil with the rotational speed of the reference oil under the same conditions.The measurements provide an indication of the ease with which the engine will turn at lowtemperatures and with limited available starting power In the case of very viscous fluids,two cylinder arrangements with a small clearance might be impractical because of the veryhigh viscous resistance; thus a single cylinder is rotated in a fluid and measurements arecalibrated against measurements obtained with reference fluids
· Cone on Plate Viscometer
The cone on plate viscometer consists of a conical surface and a flat plate Either of thesesurfaces can be rotated The clearance between the cone and the plate is filled with the fluid
Trang 5and the cone angle ensures a constant shear rate in the clearance space The advantage of thisviscometer is that a very small sample volume of fluid is required for the test In some ofthese viscometers, the temperature of the fluid sample is controlled during tests This isachieved by circulating pre-heated or cooled external fluid through the plate of theviscometer These viscometers can be used with both Newtonian and non-Newtonian fluids
as the shear rate is approximately constant across the gap The schematic diagram of thisviscometer is shown in Figure 2.15
The dynamic viscosity can be estimated from the formula:
where:
η is the dynamic viscosity [Pas];
r is the radius of the cone [m];
M is the shear torque on the cone [Nm];
ω is the angular velocity [rad/s];
α is the cone angle [rad];
k is the viscometer constant, usually supplied by the manufacturer [m-3]
Cone
Driving motor
Torque spring
Plate
α
Test fluid
The dynamic viscosity can be estimated from the formula:
Trang 6η = 2r 2 (ρ b − ρ)gF / 9v (2.18)where:
η is the dynamic viscosity [Pas];
r is the radius of the ball [m];
ρb is the density of the ball [kg/m3];
ρ is the density of the fluid [kg/m3];
g is the gravitational constant [m/s2];
v is the velocity of the ball [m/s];
F is the correction factor
Liquid level
Small hole
Sphere
Guide tube
Glass tube
Water bath
Timing marks Start
Stop
FIGURE 2.16 Schematic diagram of a ‘Falling Ball Viscometer’
The correction factor can be calculated from the formula given by Faxen [19]:
F = 1 − 2.104(d/D) + 2.09(d/D) 3 − 0.9(d/D) 5 (2.19)where:
d is the diameter of the ball [m];
D is the internal diameter of the tube [m]
There are also many other more specialized viscometers designed to perform viscositymeasurements, e.g under high pressures, on very small volumes of fluid, etc They aredescribed in more specialized literature [e.g 21]
2.8 VISCOSITY OF MIXTURES
In industrial practice it might be necessary to mix two similar fluids of different viscosities in
order to achieve a mixture of a certain viscosity The question is, how much of fluid ‘A’
Trang 7should be mixed with fluid ‘B’ This can simply be worked out by using ASTM viscosity
paper with linear abscissa representing percentage quantities of each of the fluids Theviscosity of each of the fluids at the same temperature is marked on the ordinate on each side
of the graph as shown in Figure 2.17 A straight line is drawn between these points andintersects a horizontal line which corresponds to the required viscosity A vertical line drawnfrom the point of intersection crosses the abscissa, indicating the proportions needed of thetwo fluids In the example of Figure 2.17, 20% of the less viscous component is mixed with80% of the more viscous component to give the ‘required viscosity’
FIGURE 2.17 Determining the viscosity of a mixture
2.9 OIL VISCOSITY CLASSIFICATION
There are several widely used oil viscosity classifications The most commonly used are SAE(Society of Automotive Engineers), ISO (International Organization for Standardization) andmilitary specifications
SAE Viscosity Classification
The oils used in combustion engines and power transmissions are graded according to SAEJ300 and SAE J306 classifications respectively A recent SAE classification establishes elevenengine oil and seven transmission oil grades [34,35] The engine oil viscosities for differentSAE grades are shown in Table 2.4
Note that the viscosity in column 2 (Table 2.4) is the dynamic viscosity while column 3shows the kinematic viscosity The low temperature viscosity was measured by the ‘cold-cranking simulator’ and is an indicator of cold weather starting ability The viscositymeasurements at 100°C are related to the normal operating temperature of the engine The
oils without a ‘W’ suffix are called ‘monograde oils’ since they meet only one SAE grade The oils with a ‘W’ suffix, which stands for ‘winter’, have good cold starting capabilities For
climates where the temperature regularly drops below zero Celsius, engine and transmissionoils are formulated in such a manner that they give low resistance at start, i.e their viscosity
is low at the starting temperature Such oils have a higher viscosity index, achieved by
adding viscosity improvers (polymeric additives) to the oil and are called ‘multigrade oils’.
For example, SAE 20W/50 has a viscosity of SAE 20 at -18°C and viscosity of SAE 50 at 100°C
as is illustrated in Figure 2.18 The problem associated with the use of multigrade oils is thatthey usually shear thin, i.e their viscosity drops significantly with increased shear rates due
to polymeric additives added This has to be taken into account when designing machine
Trang 8components lubricated by these oils The drop in viscosity can be significant, and with someviscosity improvers even a permanent viscosity loss at high shear rates may occur due to thebreaking up of molecules into smaller units The viscosity loss affects the thickness of thelubricating film and subsequently affects the performance of the machine.
TABLE 2.4 SAE classification of engine oils [34]
SAE 30
SAE 20
SAE 10
FIGURE 2.18 Viscosity-temperature graph for some monograde and multigrade oils (not to
scale, adapted from [12])
SAE classification of transmission oils is very similar to that of engine oils The onlydifference is that the winter grade is defined by the temperature at which the oil reaches the
Trang 9viscosity of 150,000 [cP] This is the maximum oil viscosity which can be used withoutcausing damage to gears The classification also permits multigrading The transmission oilviscosities for different SAE grades are shown in Table 2.5 [35].
TABLE 2.5 SAE classification of transmission oils [35]
FIGURE 2.19 Comparison of SAE grades of engine and transmission oils
ISO Viscosity Classification
The ISO (International Standards Organization) viscosity classification system was developed
in the USA by the American Society of Lubrication Engineers (ASLE) and in the UnitedKingdom by The British Standards Institution (BSI) for all industrial lubrication fluids It isnow commonly used throughout industry The industrial oil viscosities for different ISOviscosity grade numbers are shown in Table 2.6 [36] (ISO 3448)
2.10 LUBRICANT DENSITY AND SPECIFIC GRAVITY
Lubricant density is important in engineering calculations and sometimes offers a simpleway of identifying lubricants Density or specific gravity is often used to characterize crudeoils It gives a rough idea of the amount of gasoline and kerosene present in the crude Theoil density, however, is often confused with specific gravity
Specific gravity is defined as the ratio of the mass of a given volume of oil at temperature ‘t 1’
to the mass of an equal volume of pure water at temperature ‘t 2’ (ASTM D941, D1217, D1298)
Trang 10TABLE 2.6 ISO classification of industrial oils [36].
Kinematic viscosity limits [cSt] at 40°C
ISO viscosity grade
Density, on the other hand, is the mass of a given volume of oil [kg/m3]
In the petroleum industry an API (American Petroleum Institute) unit is used which is aderivative of the conventional specific gravity The API scale is expressed in degrees which insome cases are more convenient to use than the specific gravity readings The API specificgravity is defined as [23]:
where:
s is the specific gravity at 15.6°C (60°F)
As mentioned already the density of a typical mineral oil is about 850 [kg/m3] and, since thedensity of water is about 1000 [kg/m3], the specific gravity of mineral oils is typically 0.85
2.11 THERMAL PROPERTIES OF LUBRICANTS
The most important thermal properties of lubricants are specific heat, thermal conductivityand thermal diffusivity These three parameters are important in assessing the heating effects
in lubrication, i.e the cooling properties of the oil, the operating temperature of the surfaces,etc They are also important in bearing design
Specific Heat
Specific heat varies linearly with temperature and rises with increasing polarity or hydrogenbonding of the molecules The specific heat of an oil is usually half that of water For mineraland synthetic hydrocarbon based lubricants, specific heat is in the range from about 1800[J/kgK] at 0°C to about 3300 [J/kgK] at 400°C For a rough estimation of specific heat, thefollowing formula can be used [5]:
Trang 11σ = (1.63 + 0.0034θ) / s 0 5 (2.21)where:
σ is the specific heat [kJ/kgK];
θ is the temperature of interest [°C];
s is the specific gravity at 15.6°C
Thermal Conductivity
Thermal conductivity also varies linearly with the temperature and is affected by polarityand hydrogen bonding of the molecules The thermal conductivity of most of the mineraland synthetic hydrocarbon based lubricants is in the range between 0.14 [W/mK] at 0°C to0.11 [W/mK] at 400°C For a rough estimation of a thermal conductivity the followingformula can be used [5]:
where:
K is the thermal conductivity [W/mK];
θ is the temperature of interest [°C];
s is the specific gravity at 15.6°C
χ is the thermal diffusivity [m2/s];
K is the thermal conductivity [W/mK];
ρ is the density [kg/m3];
σ is the specific heat [J/kgK]
The values of density, specific heat, thermal conductivity and thermal diffusivity for sometypical materials are given in Table 2.7
2.12 TEMPERATURE CHARACTERISTICS OF LUBRICANTS
The temperature characteristics are important in the selection of a lubricant for a specificapplication In addition the temperature range over which the lubricant can be used is ofextreme importance At high temperatures, oils decompose or degrade, while at lowtemperatures oils may become near solid or even freeze Oils can be degraded by thermaldecomposition and oxidation During service, oils may release deposits and lacquers oncontacting surfaces, form emulsions with water, or produce a foam when vigorouslychurned These effects are undesirable and have been the subject of intensive research Thedegradation of oil does not just affect the oil, but more importantly leads to damage of thelubricated equipment It may also cause detrimental secondary effects to the operatingmachinery A prime example of secondary damage is corrosion caused by the acidity ofoxidized oils The most important thermal properties of a lubricant are its pour point, flash
Trang 12point, volatility, oxidation and thermal stability, surface tension, neutralization number andcarbon residue.
TABLE 2.7 Density, specific heat, thermal conductivity and thermal diffusivity values for
some typical materials
Pour Point and Cloud Point
The pour point of an oil (ASTM D97, D2500) is the lowest temperature at which the oil willjust flow when it is cooled In order to determine the pour point the oil is first heated toensure solution of all ingredients and elimination of any influence of past thermaltreatment It is then cooled at a specific rate and, at decrements of 3°C, the container is tilted
to check for any movement The temperature 3°C above the point at which the oil stopsmoving is recorded as the pour point This oil property is important in the lubrication of anysystem exposed to low temperature, such as automotive engines, construction machines,military and space applications When oil ceases to flow this indicates that sufficient waxcrystallization has occurred or that the oil has reached a highly viscous state At this stagewaxes or high molecular weight paraffins precipitate from the oil The waxes form theinterlocking crystals which prevent the remaining oil from flowing This is a critical pointsince the successful operation of a machine depends on the continuous supply of oil to themoving parts The viscosity of the oil at the pour point is usually very large, i.e severalhundred [Pas] [24], but the exact value is of little practical significance since what is important
is the minimum temperature at which the oil can be used
The cloud point is the temperature at which paraffin wax and other materials begin toprecipitate The onset of wax precipitation causes a distinct cloudiness or haze visible in thebottom of the jar This occurrence has some practical applications in capillary or wick fedsystems in which the forming wax may obstruct the oil flow It is limited only to thetransparent fluids since measurement is based purely on observation If the cloud point of an
oil is observed at a temperature higher than the pour point, the oil is said to have a ‘Wax Pour Point’ If the pour point is reached without a cloud point the oil shows a simple
‘Viscosity Pour Point’.
There is also another critical temperature known as the ‘Flock Point’, which is primarily
limited to refrigerator oils It is the temperature at which the oil separates from the mixturewhich consists of 90% refrigerant and 10% oil The Flock point provides an indication of howthe oil reacts with a refrigerant, such as Freon, at low temperature