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2004
Foreword
This literature study forms a part of the work in the PROGNOS- project of prognostics for
industrial machinery availability (Official title in Finnish: Teollisuuden käynnissäpidon
prognostiikka), particularly in relation to the case dealing with monitoring of erosive wear of
screen cylinders. The authors wish to express their gratitude to Tekes - National Technology
Agency of Finland, the industrial partners and VTT Technical Research Centre of Finland for
funding the project.
Authors
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Table of contents
1 Introduction ...................................................................................................... 4
References ................................................................................................................ 24
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1 Introduction
In many industrial applications components are subjected to erosive wear caused by fluid
flow. Wear resistant coatings may be applied to increase the component life time. When the
coating fails the wear rate usually increases rapidly, resulting in a fast deterioration of the
performance of the component. In case the coating wear could be monitored such that the
coating failure could be detected early enough to prevent wear of the substrate material,
recoating of the component could be possible and feasible. In this report modes of erosion,
methods for erosion testing, erosive wear of coatings and possible methods for monitoring the
coating wear particularly under slurry erosion are reviewed on the basis of literature.
Many of the erosion modes can be said to be related to each other. Sometimes it is difficult, or
even impossible, to define the actual erosion mode. The erosion mechanism depends on the
material and is different for brittle and ductile materials, and therefore erosion has been
divided into brittle and ductile erosion. Most wear models and equations are inadequate to
predict erosion. Meng and Ludema [1995] evaluated a number of wear equations and selected
28 erosion equations for a more detailed study. These contained 33 parameters, with an
average of five parameters per equation. The parameters included density and hardness of the
particle, moment of inertia, roundness, single mass, size, velocity, rebound velocity, kinetic
energy (KE) of particle, density and hardness of the surface material, flow stress, Young's
modulus, fracture toughness, critical strain, depth of deformation, incremental strain per
impact, thermal conductivity, melting temperature, enthalpy of melting, cutting energy,
deformation energy, erosion resistance, heat capacity, grain molecular weight, Weibull flaw
parameter, Lamé constant, grain diameter, impact angle, impact angle maximum wear, and
KE transfer from particle to target. All the equations also contained one or more constants,
either to form a ‘numerical bridge’ between the calculated and measured values, or to
represent specific quantitative phenomena not readily measurable. They explored several
methods trying to harmonize existing equations:
• The incidence of use of variables: hardness is the most widely used, but it is
inadequate as the only material property and not applicable for all types of wear.
• Dimensional analysis: by assuring dimensional compatibility in equations it is
expected that some forgotten variables could be found or some candidate variables
could be appropriate for consideration.
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• Superposition: adding or multiplying a new variable to the existing ones may work
for some variables, but there is too much interdependence between some variables.
• The methods of waveform analysis or system identification: very little value in
developing wear equations, because these techniques do not identify the basic
mechanisms.
• Expert system methods: these depend on an orderly construct of information and
hence cannot impose order into a system.
The result of the evaluation by Meng and Ludema [1995] was that there appears to be no such
way that could be used for harmonizing the existing equations without beginning the
modelling process in some new way.
In the following, various erosion modes are described according to the erosive medium.
ASTM G40 standard defines liquid impingement erosion as “progressive loss of original
material from a solid surface due to continued exposure to impacts by liquid drops or jets”.
This definition excludes erosion mechanisms due to:
• The impingement of a continuous jet
• The flow of a single-phase liquid over or against a surface
• A cavitating flow
• A jet or flow containing solid particles.
However, also these mechanisms can cause erosion under some conditions. Liquid
impingement erosion and solid particle erosion are quite different mechanisms, and the latter
is described in the next chapter. Discrete impacts cause far higher impulsive contact pressures
to the surface than continuous jets and the endurance limit and yield strength of the surface
can be easily exceeded. Solid material can be removed from a surface even by a single
droplet, if the impact velocity is sufficiently high. By comparison of test data it has been
estimated that the erosion rate due to droplets can be from one to five orders of magnitude
higher than the erosion rate due to a continuous jet with the same quantity of liquid impinging
the surface at the same velocity. Liquid impingement erosion can result in a surface composed
of sharp peaks and pits [Heymann 1992].
Cavitation is defined as the formation and subsequent collapse of cavities or bubbles within a
liquid, and cavitation erosion is the mechanical damage of a solid surface caused by cavities
or bubbles collapsing either at or near the surface [ASTM G40-99, Hansson 1992]. Liquid
impingement erosion and cavitation erosion damages have many similarities, both being due
to small-scale liquid/solid impacts, and sometimes it is difficult to say if the erosion
mechanism was impingement or cavitation erosion. Sometimes it is impossible to explain the
material loss situation only by mechanical action. The term “Impingement attack” is
sometimes used for material loss when the forces of unsteady, turbulent, or bubbly flows are
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believed to remove the protective oxide layers, allowing continuing and accelerating
corrosion. In situations of both corrosion and erosion acting simultaneously, the material loss
rates can be much higher than the sum of the rates of the individual processes [Heymann
1992].
To assist in the selection of materials, information of the relative erosion resistance of metallic
alloys can be obtained. Protection against erosion by shielding or cladding is usually achieved
with a harder layer than the base material, or by a composition or microstructure which is
more erosion resistant. In some low-intensity environments elastomeric coatings can be used
to reduce the impact pressures [Heymann 1992].
Solid particle erosion involves an eroding surface, the particles producing erosion, and the
fluid flow bringing the particles into contact with the surface. The factors affecting pure
erosion, i.e. erosion in the absence of corrosion, are the following [Finnie 1995]:
• Variables describing the particle flow: particle velocity, angle of incidence, particle
rotation, particle concentration in the fluid, nature of the fluid, and fluid temperature
• Particle properties: particle shape, size, hardness, and strength (or resistance to
fragmentation)
• Properties of the surface: shape, stress level, residual stress, temperature, stress as a
function of strain, strain rate and all material properties of the surface such as
hardness, fracture toughness, fatigue, melting point, microstructure etc.
The erosion resistance of ductile and brittle materials differs remarkably from each other
when measured as a function of the impact angle: ductile materials have a maximum erosion
rate at low angles of incidence while brittle materials have the maximum at or near 90° [Kosel
1992].
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In addition to wear purely caused by the slurry moving past the material or the material
moving through the slurry, other wear modes are also encountered when parts or components
are subjected to slurries. According to Miller [1992], the most common wear modes are those
described in Table 1.
2.4 Erosion/Corrosion
An important aspect in erosion-corrosion interaction is the potential synergy between the two
processes. Corrosion may enhance the erosion rate through preferential dissolution or it may
also inhibit erosion through the formation of a passive film. To describe the erosion-corrosion
interactions in aqueous environments, erosion-corrosion maps have been developed and they
identify the regimes of interactions [Stack & Jana 2004]. Erosion-corrosion interaction
regimes can be divided into pure erosion, corrosion-affected erosion, erosion-enhanced
corrosion, and pure corrosion. Pure erosion occurs when the corrosion rate is negligible as in
severe erosion conditions, for example in case of high velocity or angular particles, or in non-
corroding conditions. In corrosion-affected erosion there is an increased corrosion component.
The dimensions of the stress field caused by the particles is greater than the scale thickness
and the metal loss rate is increased when compared with pure erosion. Erosion-enhanced
corrosion is divided into different categories: a steady-state scale thickness, determined by the
relative erosion and corrosion rates, and spalling of the scale. In pure corrosion, the ratio of
corrosion to erosion rate is very high, resulting in pure corrosion and parabolic scale
thickening [Kosel 1992].
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Table 1. The common wear modes under slurry conditions according to [Miller 1992].
3 Erosion testing
For acquiring more knowledge about erosive wear on machine components, experimental
research has been carried out and several standardised test methods have been developed. The
experimental research includes both component tests in actual operational environments and
laboratory experiments under conditions simulating some defined operational conditions.
Laboratory experiments are less expensive than field testing, and the risk encountered with is
smaller in the laboratory experiments. It is easier to make conclusions on the influence of
individual operational parameters on a wear mechanism after a laboratory test than after a
field test, while on the other hand the conditions are closer to reality in a field test than in a
laboratory experiment. Normally, a compromise for the level of tribological experimental
testing has to be made.
Field tests related to erosion studies are typically based on an exchangeable machine
component or sample in a realistic process, e.g. a propeller, a pipe line or some other surfaces
subjected to a slurry in motion. An example of tests in a large fan has been presented by
Bulloch and Callagy [1999]. Results of field tests and laboratory testing related to slurry
erosion of stainless steel pipes have been presented by Wood and Jones [2003].
Laboratory experiments have been performed using different configurations, the only feature
in common being a fluid sample and a test sample surface in relative motion one to another.
In laboratory tests, either the fluid or the test sample surface is the moving part that provides
preconditions for fluid particle collisions on the sample surface.
The common method to evaluate the magnitude of the erosion wear rate is by determining the
mass loss of the test sample during the test. In terms of coated surfaces, where the penetration
of the coating may lead to a sudden increase in the wear rate, the thickness reduction of the
coating is a relevant measure for the erosive wear rate.
Intercomparisons of results from erosion tests with different test equipment, or different
procedures with the same equipment, is often unreliable. The reason for this is, in most cases,
the variation in the key parameters responsible for the erosion; minor variations in the particle
velocity and flow direction, and the particle density, size and shape may strongly influence on
the erosive wear. For this reason, the most appropriate way of comparing test results is to use
reference materials that are tested at the same time or at identical conditions as the samples
for the investigation, and in addition to this the testing conditions should be modelled if more
than a single test method and equipment is used in a study.
In the following, some examples of laboratory tests to study erosion are presented.
standardised test procedures for studies on erosion with relevance for the operational
reliability of machines are presented, with a sub-division into gas and liquid erosion.
The interaction of solid particles with surfaces under dry conditions is furthermore the issue
of the following standard on low-stress abrasive wear testing:
• ASTM G65-00, which defines a "Standard test method for measuring abrasion using the
dry sand / rubber wheel apparatus". In this test, a test sample (coated or uncoated) is
pressed against a rotating rubber wheel, while quartz sand is flowing into the gap between
the wheel and sample, see Fig. 3.2.
Fig. 3.1. The principle for sand-blast and slurry jet erosion tests.
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Fig. 3.2. An ASTM G65 rubber wheel and quartz sand abrasion test in action.
The interaction of a slurry containing abrasive particles with surfaces under wet conditions is
furthermore the issue of the following standard on low-stress slurry abrasion wear testing:
• ASTM G75-01, which defines a "Standard test method for determination of slurry
abrasivity (Miller Number) and slurry abrasion response of materials (SAR Number)".
The test employs a crank-driven reciprocating testing machine with a shallow container
for the slurry. The test specimen, in the shape of a cylinder with a circular test surface,
slides in an oscillating mode, submerged in the abrasive slurry, under pressure against a
Neoprene (™DuPont) rubber surface.
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Fig. 3.3. The principle for whirling-arm-rig and slurry pot erosion tests.
towards the surface of the sample plates by the Coriolis effect. The Coriolis slurry erosion
tester offers good reproducibility and good discrimination between materials of different
erosive wear resistance [Hawthorne 2002, Hawthorne et al. 2003, Clark et al. 2000,
Llewellyn et al. 2004]. The action of the erodent in the Coriolis slurry erosion tester has
been studied in detail by Hawthorne et al. [2002] and modelled by Xie et al. [1999].
• A double cylinder test rig, in which a smaller cylinder rotates inside a larger cylinder, with
a slurry in between the cylinder walls. The rotational speed can be up to 10.000 rev/min,
as an example [Stack & Wang 1999]. Because of the centrifugal action, the method is,
however, quite mild in terms of erosive wear of the inner cylinder surface.
The interaction of a slurry containing abrasive particles with surfaces under wet conditions is
furthermore the issue of the following non-standard abrasive wear test:
• Micro-abrasive wear tests for the simulation of slurry erosion has been carried out with a
wheel-on-flat geometry in a slurry environment [Xie et al. 2001].
Fig. 3.4. The principle for the Coriolis slurry erosion tester; the grey disc with flow channels
and samples is rotating with a velocity ω.
In recent years, several works on the erosion of engineering materials have been presented in
the literature on tribology. In the following, a selection of works related to the erosion of
coated surfaces is reviewed. The study is limited to metallic, ceramic, diamond and polymeric
coatings, with the emphasis on hard coatings.
Double-cylinder slurry tests by Stack et al., and mapping of the erosion-corrosion severity for
mild steel and stainless steel AISI 304 and a selection of thin ceramic coatings, has shown
that erosive-corrosive wear can be higher for carbon steel than for stainless steel, and for both
steels it can be higher than for thin ceramic coatings [Stack et al. 1999].
Cavitation erosion tests, performed by Han et al. using a piezoelectric actuator, have shown
that a hard chrome plating reduces the weight loss caused by erosion, in comparison with that
of an uncoated carbon steel or a multilayer chromium nitride and chromium (CrN/Cr) coating
on carbon steel [Han et al. 2002].
Re-circulating slurry jet tests performed by Hawthorne et al. have shown that the erosion rate
of HVOF-sprayed (high velocity oxy-fuel) metallic coatings (stainless steel 316 L, Ni-W-Cr-
Si-Fe-B-C and Co-Cr-Ni-Mo-W-Fe) was higher than for cemented carbide and Cr3C2-based
coatings in the comparison, at both 20° and 90° impingement angle [Hawthorne et al. 1999].
Slurry jet impingement tests performed by Wood and co-authors have shown that the erosion
resistance of thermally sprayed WC-Co-Cr coatings is similar to that of sintered cemented
carbide material grades when the energy impact is low, but that the erosion resistance is
weaker for the coating when the energy impact is high. At low impact energy, the impact
angle affected the wear rate of the coating, being highest at 90° impingement angle. At high
impact energy, under which conditions the erosion was stronger, the impact angle was almost
insignificant for the wear rate [Wood et al. 1997]. In a larger overview, Wood [1999] presents
thermally sprayed WC-Co-Cr coatings as the most wear resistance solution for high
impingement angles (90° angle) and high velocities, in comparison with a large range of
metallic, ceramic and polymeric coatings studied under slurry impingement erosion
conditions.
Accelerator disc erosion tests with a re-circulating slurry, which have been presented by
Mann and Arya, have shown that a thermally sprayed WC10Co5Cr HVOF coating gives less
erosive wear than an as-received or plasma nitrided 13Cr-4Ni steel surface. Work by Mann
has shown that borided steel T410 has a higher resistance against erosive wear than, for
instance, plasma nitrided or WC-coated steel 13Cr-4Ni [Mann 2000, Mann & Arya 2001].
Slurry pot tests by Lathabai and co-workers on arc sprayed thick (approx. 240 µm) oxide
ceramic coatings (Al2O3, Cr2O3) have shown that the erosive wear rate was higher for the
Al2O3 coating than for the Cr2O3 coating, and that the wear of the two ceramic coatings was
higher than for the stainless steel AISI 316 and mild steel reference materials. The erosive
wear of the ceramic coatings was stronger with harder particles (SiC) than with softer (SiO2)
particles [Lathabai et al. 1998].
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Slurry jet tests by Wood et al. on various metallic, ceramic and polymeric coatings and steel
have shown that the erosive wear rate was higher for a plasma sprayed Al2O3-TiC ceramic
coating of 1060 µm thickness than for carbon steel and stainless steel [Wood et al. 1998].
Similarly, slurry jet-in-slit tests by Zhao and co-authors have shown that the erosion of
ceramic coatings (Cr2O3, Al2O3-TiO2, ZrO2) is more severe than for stainless steel when the
slurry jet is directed towards the surface, but that the ceramic coatings, particularly Cr2O3,
have a higher erosive wear resistance than stainless steel when the jet travels along the surface
[Zhao et al. 1995, 1999a, 1999b]. Re-circulating slurry jet tests performed by Hawthorne et al.
have shown that the erosion rate of HVOF-sprayed cemented carbide and Cr3C2-based
coatings was lower than that of metallic coatings in the comparison, at both 20° and 90°
impingement angle [Hawthorne et al. 1999].
Taken together the above observations, thermally sprayed Cr2O3 coatings seem to be superior
to equally deposited Al2O3 coatings. At impingement angles closer to 90°, the ceramic
coatings do not offer any advantages over uncoated steel materials, while at impingement
angles closer to 0°, the ceramic coatings seem to offer wear protection. Harder erodent
particles cause more wear on ceramic coatings than do softer particles.
In a larger overview, Wood [1999] presents the results of a larger comparison with slurry
impingement erosion tests with a large range of metallic, ceramic, diamond and polymeric
coatings. Particularly CVD diamond coatings, but also diamond-like carbon (DLC) coatings
by physical vapour deposition (PVD), showed a high resistance against volumetric erosive
wear in slurry jet impingement tests at 90° angle, offering significant improvement in wear
resistance when compared with steel. Coating detachment turned out to be a limiting factor
for the erosion resistance of these coatings at 90° impingement angle.
extent of localised wear can also be obtained. The dimensional changes can be measured e.g.
by using profilometers (stylus or optical, also for three-dimensional profiling) or optical
microscope determination of wear scar dimensions. Small micro-hardness indentations or
scratches of different controlled depths can also be used to determine the extent of wear by
determining how the size of the indents or scratches reduces during the wear exposure
[Rabinowicz 1995, Ruff 1997].
In the case of coatings, the amount of wear could also be determined by measuring the coating
thickness before and after the wear exposure. A variety of methods, both standardised and
non-standardised, exist for coating thickness measurements based on e.g. optical methods
(optical microscopy or scanning electron microscopy of cross sections), material removal
(ball cratering, coulometric method by anodic dissolution, step height profilometry),
electromagnetic methods (eddy current, magnetic flux, capacity), as well as scattering or
excitation (beta back scattering, ultrasonic, x-ray fluorescence) [Holmberg & Matthews 1994,
ISO 3882].
The above methods can be used for monitoring coating wear mainly in situations where the
test or process can be stopped periodically and the samples removed for measurement, for
example during laboratory tests. The use of replica techniques would allow dimensional
changes to be measured also in situ, by periodically cleaning the worn surface and taking
replica samples from it. When on-line monitoring of wear is required, direct measurement of
weight loss or dimensional changes is more difficult or even impossible, and often indirect
methods are more feasible. The present literature search on wear monitoring of coatings gave
fairly little results in other areas except for tool wear monitoring during machining, which is a
subject of intensive research. For tool wear monitoring, a number of indirect methods such as
e.g. measuring forces, vibration, acoustic emission and sound, are used [Dimla 2000, Jantunen
2002]. Methods for direct wear measurement based on machine vision have also been
developed [Kurada & Bradley 1997, Lanzetta 2001].
Some corrosion monitoring methods should also be applicable for monitoring erosive wear of
coated components under wet conditions, e.g. during slurry erosion. Even if the measurements
would indicate a corrosion rate which is lower than that of the actual wear rate due to erosion,
an indication of the break through of the coating should be possible to be obtained by some
corrosion monitoring methods. Erosion-corrosion processes of coated samples have been
studied by using electrochemical methods which have also been able to respond to coating
breakdown [Wood et al. 2002].
In the following, methods which could be suitable for on-line monitoring of coating wear are
reviewed with focus on methods which are applicable for metallic or other inorganic coatings
under slurry erosion.
In linear polarization resistance (LPR) measurement the current needed to maintain a specific
voltage shift, typically of the order of 10 mV, is measured while a small voltage (or
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Electrochemical noise (EN) arises from the random fluctuations in potential and current
during an electrochemical process. The electrochemical potential is related to the driving
force of the reaction whereas the current is related to the corrosion rate (kinetics of the
reaction). One of the advantages of the use of EN measurements is the fact that localized
corrosion processes, which may be difficult to monitor with other techniques, tend to give
particularly strong EN signals, and the method can be used to predict the type and severity of
corrosion that is taking place [Holcomb et al. 2004, Cottis & Llewellyn 1996].
Electrochemical current noise can be measured between a pair of identical electrodes, or on a
single electrode under potentiostatic control. When using two similar working electrodes,
both current and potential noise can be measured simultaneously since the potential noise of
the working electrode pair, both electrodes being at the same potential, can be measured with
respect to a third working electrode or a reference electrode [Holcomb et al. 2004, Cottis &
Llewellyn 1996, Wood et al. 2002]. EN measurements have been successfully applied for e.g.
the investigation of corrosion-wear of stainless steel under oscillating sliding conditions [Wu
& Celis 2004] and of erosion-corrosion processes of stainless steel with a thermally sprayed
coating, showing also clear response on coating breakdown [Wood et al. 2002]. Detection of
localised corrosion or corrosion type by EN method has been studied by Cottis et al., for
instance in the references [Cottis et al. 2001, Al-Mazeedi & Cottis 2004].
Electrical resistance (ER) monitoring is another method which can be used for on-line
measurement of corrosion, and it is also suitable for situations where the metal loss is due to
mechanical processes such as erosion. Metal loss from the surface of a measuring element
results in a decrease of the cross-sectional area of the element, with a corresponding increase
in its electrical resistance. The rate of change of the resistance is a measure of the rate of
metal loss due to corrosion, erosion or some other form of wear. ER measurements can be
made either periodically or continuously. Since actual metal loss must occur before a response
is obtained, this method may be somewhat slower than electrochemical measurements
[Cowan & Winer 2001, MSC 2004, Caproco 2004].
filter or trap or in the fluid line. In the marker approach, wear can be measured directly by
placing a detector to indicate the activity remaining in the activated part [Blatchley 1992].
Activation of the monitored sample or component can be carried out by neutrons in a nuclear
reactor, which usually results in the part becoming thoroughly radioactive. Alternatively, if
activation is performed by heavy charged particles such as protons, deuterons or alfa-particles
using a cyclotrone, only a thin surface layer of the component will be activated. The
advantage of thin layer activation is that the total activity of the components remains low,
hence reducing the need for special protective measures [Scherge 2003]. The activated thin
surface layer acts as a marker, allowing wear measurement from the remaining activity of the
component. When the marker is very shallow, a precision in the order of 1% of the activated
depth can be achieved in wear measurements. Ultra-shallow activated layers can be produced
by recoil implantation, which is a process where a target foil is bombarded instead of the
actual part. Reaction products in the foil recoil with enough energy to escape and be
implanted downstream to the surface of the part, which is being activated. This method is very
suitable to materials that are easily degraded due to radiation damage. With surface layer
activation, both marker and tracer approaches can be used whereas the use of neutron
activation is mostly restricted to the tracer method unless the material to be activated is
already in a thin coating [Blatchley 1992].
The advantages of the surface layer activation include the high precision possible, especially
for markers, and the fact that both marker and tracer readings can be taken in-situ without
interfering with the experimental system or process. Critical properties of gamma-emitting
radionuclides that determine their suitability for wear monitoring, are their half-life and
gamma-ray energy. The rate of decay must be slow enough to allow a reliable signal to persist
throughout the planned measurement interval. For quick tests, half-lives of a few days are
sufficient. For long-term monitoring, reliable measurements can typically be made for up to
six half-lives. If a component being monitored is contained within some material around it,
the gamma radiation must be sufficiently energetic to penetrate the surrounding material to
allow detection from the outside [Blatchley 1992].
The radionuclide technique has been successfully applied to many engine components and
even to large industrial systems [Blatchley 1992, Scherge 2003, Schneider et al. 2003]. A
short introduction to the surface layer activation technique by Blatchley can be found from
reference [Blatchley 2004].
Optical sensors can be divided into intrinsic and extrinsic devices. In the former, the
interaction occurs within an element of the optical fiber itself, whereas in the latter the optical
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fiber is used to couple light, usually to and from the region where the light beam is influenced
by the measurand. In many sensor systems the parameter of interest is measured at a specific
location. This ‘point’ measurement capability is the most common sensor operation mode,
used for example when monitoring temperature, pressure, acceleration, or many chemical
parameters. This is also how many fiber optic sensors operate: the sensor tip may be
sensitized via a chemical indicator to respond to pH, the sensor may have a prism tip for
liquid level monitoring, or resonant structures may be mounted at the end of the fiber for
pressure or acceleration measurement, to mention a few examples. Fiber optic sensing
techniques offer also possibilities for distributed sensing, as a result of the ability to spatially
discriminate the measurand at different locations along the length of the fiber itself. Most
distributed fiber optic methods utilise non-linear optical effects in the fiber material, since
these exhibit varied and distinctive responses to external measurands. Distributed sensing has
been employed for example in some types of strain sensing as well as for temperature
measurements. If the fiber is not sensitive along its entire length, but is locally sensitized at
particular predetermined points along the length of the fiber network, a ‘quasi-distributed’
sensor system is obtained. This technique has been applied to pressure and chemical sensing,
e.g. using different fiber types.
The common feature of fiber optic sensors is that they contain an optical fiber, at least one of
a range of optical sources and a modulation scheme by which the parameter that is being
measured introduces a change in the optical signal, which can be sensed at the detector and
employed through the signal processing scheme. For example, the operation of interferometric
sensors is based on the measurand-induced phase shift proportional to the influence of the
measurand on the optical system (e.g. strain or temperature induced change in fibre length or
optical path). Fibre Bragg gratings (FBG) are simple intrinsic devices photo-inscribed into a
fiber, and they form one of the most intresting development areas in fiber optic sensors,
particularly in the area of embedded sensing in materials for creating smart structures. They
are based on the photosensitivity of silica fiber doped with germanium when illuminated with
UV light. Absorption of UV light causes a change in the absorption characteristics of the glass
resulting in a shift in the index of the glass at certain wavelengths. Illuminating the glass with
a broadband source of light, a narrowband component is reflected at the Bragg wavelength.
Perturbation of the grating, e.g. as a result of temperature or strain, results in a shift in the
Bragg wavelength of the device. This shift can be detected in either the reflected or
transmitted spectrum.
One advantage of fiber optic sensors is the relative ease of multiplexing of several fibres into
an array that uses a common source and detection system. The three major multiplexing
arrangements that may be used are wavelength division (WDM), frequency division (FDM),
and time division (TDM). The number of sensors on a single network can be extended by
using various combinations of the multiplexing techniques.
More detailed descriptions of the various fibre optic sensors and their possibilities can be
found in the before mentioned review articles [Kersey 1996, Grattan & Sun 2000] as well as
in the numerous references in them. Even if it is not possible to utilise fibre optic sensors to
direct wear monitoring of coatings they should provide a possibility at least for the detection
of coating break through by embedding the fibres between the coating and the substrate. The
distributed sensor system could in some applications possibly even allow the determination of
the location of the coating damage.
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The wear range measured by Yaxley and Knight [1999] was around 50 mm and the accuracy
they achieved was in the range of 1 mm. In many applications there is, however, a need to
monitor wear in much smaller dimensions. In order to be able to monitor the wear of a sliding
bearing surface while in contact with a shaft or flat counter face, Kreider and Ruff have
studied sensors consisting of electrically conductive films separated from the bearing with
insulating films [Kreider & Ruff 1996, Ruff & Kreider 1997]. Wear was quantified by
changes in the electrical resistance of the sensor due to the reduction of the thickness of the
conducting film. A constant current was fed to the conducting film and the resistance was
recorded throughout the test. Most of the increase in the resistance of a single layer was
measured during the last 20% of its life. Wear-through of the conducting film was indicated
by a high resistance value. The performance and resolution of the sensor can be enhanced by
using multilayer-laminated thin-films. As the initial thickness of each layer in the laminate is
known, the progression of wear can be followed when each conducting layer wears through.
The sensor must not change the performance of the shaft or bearing which is measured. This
can be achieved by both miniaturization of the sensor such that its area is an insignificant
fraction of the wear surface and by selecting the sensor materials such that their wear
resistance is comparable to that of the substrate material. Commercial electrical conductor
thin-films can be produced with line widths of about 0.1 mm using metal shadow masks, and
much smaller line widths can be achieved by photolithography. The thickness of the sensor
can be designed to be the same as that of the wear depth to be measured.
The smart sensors described above can be used for measuring local wear on the location
where they are placed. Hence the use of this type of sensors is mainly restricted to
applications where the critical wear location is known or the wear is uniform.
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6 Conclusions
The parameters affecting erosion are diverse and include material properties, environmental
factors and process parameters. The erosion modes were reviewed according to the media
causing erosion, i.e. liquid impingement erosion, cavitation erosion, solid particle erosion,
slurry erosion and the combination of erosion and corrosion.
Comparison of the results of different erosion tests is often unreliable, due to the wear being
strongly influenced by the variation of key parameters responsible for it. Even minor
variations in e.g. particle velocity and flow direction may have a strong influence on erosion
test results. The use of reference materials that are tested at the same time or at identical
conditions as the test samples is advisable for enabling comparison of results. A number of
both standardised and non-standardised erosion tests exist. Test procedures for erosion studies
with relevance for the operational reliability of machines are presented in the report, with a
sub-division into gas and liquid erosion.
Erosion of coated surfaces has been studied by a number of authors showing that hard
metallic coatings such as hard chrome plating and ceramic coatings can be successfully used
to increase the erosion resistance of steels. However, in many cases thin ceramic coatings
offer less protection against slurry erosion than the other groups of hard coatings. Thick
ceramic coatings seem to offer wear protection at low impingement angles but not at angles
close to 90o. Diamond and diamond-like coatings can be used to increase erosion wear
resistance, the coating detachment being the main limitation to their ability for wear
protection.
The most common methods to measure wear involve direct determination of the amount of
removed material as mass loss or volume loss. Due to differences in density, comparison of
wear between different materials is, however, easier by dimensional changes or volume loss
than by mass loss. Dimensional changes can be used for determining wear distribution or
localised wear, and for coatings the reduction of coating thickness is a useful indication of
wear. When on-line monitoring of wear is required, indirect methods are often more feasible.
On-line corrosion monitoring methods could also be applicable for monitoring wear under
slurry erosion. Even if the measurements would indicate a corrosion rate which is lower than
that of the actual wear rate due to erosion, an indication of the break through of the coating
should be possible by some corrosion monitoring methods. Other methods possibly suitable
for being adapted to on-line monitoring of coating wear under slurry erosion include
radionuclide technique, fibre optic sensors and smart sensors based on capacitive, resistive or
conductive principles.
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