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Studies on Aluminum-Fly-Ash Composite Produced by Impeller Mixing

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A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF
Master of Technology
In Metallurgical & Materials Engineering
Submitted By
Shuvendu Tripathy Roll No.207MM103
Under the guidance of Prof.S.Sarkar
Department of National Metallurgical & Materials Institute of Technology Rourkela 2009
National Institute of Technology Rourkela

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ABSTRACT
Metal matrix composites (MMCs) constitute an important class of design and weight-efficient structural materials that are encouraging every sphere of engineering applications. There has been an increasing interest in composites containing low density and low cost reinforcements. Among various discontinuously dispersed solids used, fly ash is one of the most inexpensive and low density reinforcement available in large quantities as solid waste by-product during combustion of coal in thermal power plants. Hence, composites with fly ash as reinforcement are likely to overcome the cost barrier for wide spread applications in automotive and small engine applications. To produce Al matrix cast particle composites, wettaility of the ceramic particles by liquid Al is essential. To improve wettabilty, elements such as Mg and Si are added into Al melt to incorporate the ceramic particles. The present investigation has been focused on the utilization abundant available industrial waste fly ash in useful manner by dispersing it into aluminium/aluminium-magnesium/aluminium-silicon matrix to produced composites by liquid metallurgy route. Wide size range (0.1-100um) fly ash particles were used. These composites were observed with the help of optical micrography, x ray micro analysis, x ray diffraction, wet chemical analysis, and image analysis. The dry sliding wear behavior of the composites in the cast conditions was studied at different loads and different sliding velocities with the help of Pin-On-Disc wear test machine. The worn surfaces and wear debris were analyzed using optical microscope and scanning electron microscope. The mechanical properties such as hardness and tensile strength have been investigated.

CHAPTER-1
Introduction
Conventional monolithic materials have limitations with respect to achievable combinations
of strength, stiffness, and density. In order to overcome these shortcomings and to meet the
ever-increasing engineering demands of modern technology, metal matrix composites are
gaining importance. In recent years, discontinuously reinforced aluminum based metal matrix
composites have attracted world wide attention as a result of their potential to replace their
monolithic counterparts primarily in automobile and energy sector. [1]
The basic idea is that continuous fiber reinforced composite has better strength but the
processing methods is highly expensive which hinders their adoption. The continuous fiber
reinforced composites do not allow secondary forming such as rolling, forging and extrusion.
As results of these limitations new efforts on the research of discontinuous reinforcements
have been used. [2, 3] At early stages of development of metal matrix composite emphasis
was given on the preparation of fiber reinforced composite only. But due to the high cost
associated with the process of production, anisotropic properties of the resultant composite
and difficulties associated with the fabrication process, production of this type of composites
has been limited. Now a days the particulate reinforced Al matrix composite are gaining
importance because of their low cost with advantage like isotropic properties. The
strengthening of aluminum alloys with dispersion of fine ceramic particulate composite
materials were developed as an alternative of unreinforced alloy, for obtaining materials with
high stiffness (high strength/modulus and low density) with special interest for the wear
resistant and structural applications. [4, 5] The dispersion strengthened alloys can be
classified, based on the size and volume % of particles uniformly dispersed in the matrix.
Aluminum alloys reinforced with ceramic particles exhibit superior mechanical properties to
unreinforced Al alloys and hence are candidate for engineering applications. The aluminum
metal matrix composites are produced either by casting route or by power metallurgy. The
former has the advantages of producing the composites as lower cost of production and
possibility of producing larger components. However, the inherent difficulties of casting
route are non wettability of ceramic particles by liquid aluminum [6], segregation of particles,
higher porosity level and extensive inter-facial reaction due to higher processing temperature.
Wettabilty of the particles can be improved by coating the particles with metals such as Ni
and Cu, addition of active elements such as Mg into liquid aluminum or preheating of the
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particles before addition into liquid aluminium [6]. The most conventional method of production of composites by casting route is vortex method, where the liquid aluminum containing 2-5% Mg is stirred with an impeller and ceramic particles are incorporated into vortex formed by stirring of the liquid metals. Addition of Mg into the liquid metal reduces the surface tension [7] and there by avoids the rejection of the particles from the melts. With out addition of Mg recovery of the particles into the melt is quite low. Hence 2-5% Mg is generally added into the Al melts before incorporation of the particles. However, the chemistry of the particles of an Al alloy is changed with addition Mg that can be deleterious to the mechanical properties of the composites.
The present investigation has been focused on utilization of waste fly ash in useful manner by dispersing it in aluminum matrix to produce composite. In the present work, fly-ash which mainly consists of refractory oxides like silica, alumina, and iron oxides, was used as the reinforcing phase and to increase the wetabbility magnesium and silicon were added. Composites were produced with different percentages of reinforcing phase. Further, these composites were characterized with the help of, optical micrography, x ray micro analysis, x ray diffraction, wet chemical analysis, and image analysis. Mechanical and wear properties of the composites were also evaluated.
CHAPTER-2
2. Literature Review
2.1 Definition of composite material:
The composite material can be defined as the system of material consisting of a mixture of combination of two or more micro constituents insoluble in each other and differing in form and or in material composition .These materials can be prepared by putting two or more dissimilar material in such way that they function mechanically as a single unit. The properties of such materials differ from those of their constituents. These materials may have a hard phase embedded in a soft phase or vice versa. Normally in the composite material have a hard phase in the soft ductile matrix where the hard phase act as a reinforcing agent increase the strength and modulus, and soft phase act as matrix material. The requirement for satisfying the above mentioned condition is
a. The composite material has to be man-made
b. The composite material must be a combination of at least two chemically distinct materials
with an interface separating the components.
c. The properties of composite should be three dimensionally combined.
2.2 Classification of Composites
2.2.1 On the basis of Matrix composite can be classified in the following groups:
a) Polymer-matrix composites (PMC)
The most common matrix materials for composites are polymeric. Polyester and viny esters are the most widely used and least expensive polymer resins. These matrix materials are basically used for fiber glass reinforced composites. For mutations of a large number resin provide a wide range of properties for these materials .The epoxies are more expensive and in addition to wide range of ranging commercials applications ,also find use in PMCs for aerospace applications. The main disadvantages of PMCs are their low maximum working temperature high coefficients of thermal expansion and hence dimensional instability and sensitivity to radiation and moisture. The strength and stuffiness are low compared with metals and ceramics. [9, 10]
b) Metal-matrix composites (MMC)
The matrix in these composites is a ductile metals .These composites can be used at higher service temperature than their base metal counterparts. These reinforcements in these materials may improve specific stuffiness specific strength, abrasion resistance, creep resistance and dimensional stability. The MMCs is light in weight and resist wear and thermal distortion, so it mainly used in automobile industry. Metal matrix composites are much more expensive those PMCs and, therefore, their use is somewhat restricted. [9, 10]
c) Ceramic-matrix composites (CMC)
One of the main objectives in producing CMCs is to increase the toughness. Ceramics materials are inherent resistants to oxidation and deterioration at elevated temperatures; were it not for their disposition to brittle fracture, some of these materials would be idea candidates for use in higher temperature and serve- stress applications, specifically for components in automobile an air craft gas turbine engines .The developments of CMCs has lagged behind mostly for remain reason, most processing route involve higher temperature and only employed with high temperature reinforcements[9].
2.2.2 On the basics of reinforcement can be classified into three types:
a) Particle reinforced composites
Particulate reinforcements have dimensions that are approximately equal in all directions .The shape of the reinforcing particles may be spherical, cubic, platelet or any regular or irregular geometry. These composite can classified under two sub groups [8]:
(i) Large particle composites
(ii) Dispersion strengthened composites
b) Fiber reinforced composites
A fibrous reinforcement is characterized by its length being much greater than its cross-sectional dimension .However the ratio of length to the cross sectional dimension know as the aspect ratio, can vary considerably .In single layer composite long fibers with high aspect ratios give that are called continuous fiber reinforced composites whereas discontinuous fiber reinforced composites are fabricated using short fibres of low aspect ratio .The orientation of the discontinuous fibres may be random or preferred .The frequently encountered preferred orientation in the case of continuous fibre composite is termed unidirectional and the corresponding random situation can be approximated to by bidirectional woven reinforcement [10].
2.3 Strengthening mechanism of composite 2.3.1 Strengthening mechanism of fiber reinforced composite Rule-Of-Mixture
Most studies concerned with the evaluation of mechanical behavior of fiber reinforced composites use what is called a "Rule-Of-Mixtures"(ROM) to predict and/or to compare the strength properties of the composite The ROM is nothing but an operational tool that uses weighted volume average of the component properties in isolation to obtain the magnitude of the property for the composite. Specifically, in the case of composite containing uniaxially aligned, continuous fibers, the composite stress is written as
Oc = Of Vf + Cm Vm (1)
Where O is the axial stress, V is the volume fraction of the component and the subscripts c, f and m refer to the composite, fiber and matrix, respectively. It is to be noted that
Vf + Vm = 1
Under conditions of isostatic, i.e, the longitudinal strain in the components being equal, one may write another ROM relationship for the elastic moduli,
Ec = Ef vf + Em Vm (2)
Where E is the elastic modulus and the subscripts represent the components as before. Eq. (2)
neglects any transverse strain arising because of the different contractile tendencies of the
components (i.e, vf = v, where v is Poisson's ratio). However, for metallic systems, the
difference in Poisson's ratio of the two components is generally insignificant and the ROM
values are generally found to be within the limits of the experimental error.
Another example of a property for which ROM works very well is the density p. One can
write as pc = pf vf + (),ž vm (3)
It would appear from these studies that the ROM as applied conventionally to the strength properties of composites with metallic matrices is not valid. The whole is more than the sum of individual components in isolation [11].
2.3.2 Strengthening mechanism of particulate composite
a) Large-particle composite
Particle-Reinforced Composites can be large-particle and dispersion-strengthened composites are the two subclassifications of particle-reinforced composites. The distinction between these is based upon reinforcement or strengthening mechanism. The term "large" is used to indicate that particle-matrix interactions cannot be treated on the atomic or molecular level; rather, continuum mechanics is used. For most of these composites, the particulate phase is harder and stiffer than the matrix. These reinforcing particles tend to restrain movement of the matrix phase in the vicinity of each particle. In essence, the matrix transfers some of the applied stress to the particles, which bear a fraction of the load. The degree of reinforcement or improvement of mechanical behavior depends on strong bonding at the matrix-particle interface.
b) Dispersion strengthened composite
For dispersion-strengthened composites, particles are normally much smaller, with diameters between 0.01 and 0.1 m (10 and 100 nm). Particle-matrix interactions that lead to strengthening occur on the atomic or molecular level. The mechanism of strengthening is similar to that for precipitation hardening. Whereas the matrix bears the major portion of an applied load, the small dispersed particles hinder or impede the motion of dislocations. Thus, plastic deformation is restricted such that yield and tensile strengths, as well as hardness, improve.
2.4. Interfacial bonding Mechanisms
Once the matrix has wet the reinforcement, and is therefore in intimate contact with reinforcement, bonding will occur A number of different types of bond may formed .The type of bonding varies from system to system and dependent on fine details such as the presence of surface contaminates or of added surface active agents . 2.4.1 Adsorption and wetting
Wettability is another significant problem when producing cast metal matrix composites. Wettability can be defined as the ability of a liquid to spread on a solid surface. Good wettability means that the liquid (matrix) will flow over the reinforcement covering every 'bump' and dip of the rough surface of the reinforcement and displacing air. It also describes the extent of intimate contact between liquid and a solid.
(Fig 2.4. Schematic diagram showing the contact angle that describes wettability) Wettability will not occur if the viscosity of the matrix is not too high and if wetting result in a decrease in the free energy of the system. Successful incorporation of solid ceramic particles into casting requires that the melt should wet the solid ceramic phase. The problem of the wetting of the ceramic by molten metal is one of surface chemistry and surface tension. The chemistry of the particle surface, including any contamination, or oxidation, the melt surface and oxide layer must be considered. All the surfaces have associated with the free energy (per unit area)
ysl= free energy per unit area of solid- liquid interfaces, ysv= free energy per unit area of
solid- vapor interfaces, ylv= free energy per unit area of liquid- vapor interfaces The spreading coefficient can be defined as
SC= Ysv - (Ysl + Ylv)
The bonding force between the liquid and solid phases can be expressed in terms of contact angle referred to in the Young-Dupre's equation [12].
Ysl +7lvCos0 2
Cos0= (Ysv- Ysl)/ Ylv 3
0 may be used as a measure of the degree of wettability.
(i) 0 =1800 , no wettability
(ii) 0 =00 , perfect wettability
(iii) 00<0<18O0, partial wettability
2.4.2 Inter-diffusion
Various types of diffusion process which promote the adhesion can take place at the interface. The diffusion of free chain ends at the interface between two polymers, which leads to chain entanglements and a rise in the adhesive strength. Inter diffusion can take place in non polymeric systems, particularly if it is accompanied by a chemical reaction. The adhesive strength dependent on the nature of the resultant inters atomic bonds. Inter-diffusion plays only a minor role at low temperatures, but at elevated temperatures approaching the melting point of the matrix, inter-diffusion and chemical reaction can result in the formation of brittle inter metallics which are detrimental to the mechanical properties of MMCs.
2.4.3 Chemical bonding
Various types of chemical reaction may occur at the interface, either deliberately or inadvertent. These bonds may be covalent, ionic, metallic, etc and in many cases very strong. These are many examples of inter facial bond strength being raised by localized chemical reactions. For strong chemical bonding between the reinforcement and matrix a controlled amount of chemical reaction at the interface is always desirable. However, too thick an inter-facial zones adversely the mechanical properties of the composites and leads to premature failure.
2.4.3 Mechanical adhesion
Mechanical interlocking or keying of two surfaces can be lead to reasonable bond. Clearly the interlocking is greater and hence the mechanical bonding more effective, the rougher the interface. Also any concentration of the matrix onto the reinforcement is favorable to bonding. Mechanical bonding plays a major role in load transfer by shear. Two separate factors affect mechanical adhesion namely (1) Surface roughness, which control the amount of mechanical interlocking that can occur, and (2) The presence of residual stresses in the matrix as a result of fabrication. In most cases a purely mechanical bond is not encountered and mechanical bonding operates in conjunction with another bonding mechanism.
2.5 Metal matrix composites
Metal-matrix composites (MMCs) are engineered combinations of two or mote materials (one of which is a metal) where tailored properties are achieved by systematic combinations of different constituents. Conventional monolithic materials have limitations in respect to achievable combinations of strength, stiffness and density .Engineered MMCs consisting of continuous or discontinuous fibres, whiskers, or particles in a metal achieve combinations of very high specific strength and specific modulus. Furthermore, systematic design and synthesis procedures allow unique combinations of engineering properties in composites like high elevated temperature strength, fatigue strength, damping property, electrical and thermal conductivities, friction coefficient, wear resistance and expansion coefficient. Structurally, MMCs consist of continuous or discontinuous fibres, whiskers, or particles in an alloy matrix which reinforce the matrix or provide it with requisite properties not achievable in monolithic alloys. In a broader sense, cast composites, where the volume and shape of phase is governed by phase diagrams, for example, cast iron and aluminum-silicon alloys, have been produced by foundries for a long time. The modern composites differ in the sense that any selected volume, shape and size properties in composites like high elevated temperature of reinforcement can be artificially introduced in the matrix. The modem composites are non equilibrium combinations of metals and ceramics, where there are fewer thermodynamic restrictions on the relative volume percentages, shapes and size of ceramic phases. Composite materials are attractive since they offer the possibility of attaining property combinations which are not obtained in monolithic materials and which can result in a number of significant service benefits. These could include increased strength, decreased weight, higher service temperature, improved wear resistance, higher elastic modulus, controlled coefficients of thermal expansion and improved fatigue properties. The quest for improved performance has resulted in a number of developments in the area of MMC fabrication technology .These includes both the preparation of the reinforcing phases and the development of fabrication techniques [13].
2.6 Fabrication techniques for metal matrix composites
A number of composite fabrication techniques have been developed that can be placed into four broad categories. These are: (i) powder metallurgical techniques, (ii) liquid metallurgy. The liquid metallurgy techniques include unidirectional solidifications to produce directionally aligned MMCs, suspension of reinforcement in melts followed by solidification, compocasting, squeeze casting, spray casting, and pressure infiltration. The liquid metallurgy techniques are the least expensive of all, and the multi-step diffusion bonding techniques may be the most expensive [14]. 2.6.1 Powder metallurgical techniques
Powder blending followed by consolidation (PM processing), diffusion bonding and vapor deposition techniques come under solid state processing Powder metallurgy techniques offer the following three advantages over liquid metallurgy techniques for fabricating MMCs.[15]
(a) Lower temperatures can be used during preparation of a PM-based composite compared with preparation of a liquid metallurgy-based composite. The result is lesser interaction between the matrix and the reinforcement when using the' PM technique. By minimizing undesirable inter-facial reactions, improved mechanical properties are obtained.
(b) In some cases, PM techniques will permit the preparation of composites that cannot be prepared by the liquid metallurgy. For instance, fibres or particles of silicon carbide will dissolve in melts of several metals like titanium, and such composites will be difficult to prepare using liquid metallurgy techniques.
© However, PM techniques remain expensive compared to liquid metallurgy techniques for the composites like AI-SiC particle composites. In addition, only small and simple shape can be produced by PM techniques.
Power blending and consolidation
Blending of metallic power and ceramic fibers or particulate has the advantage of close control over the ceramic content. Blending can be carried out dry or in liquid suspension. Blending is usually followed by cold compaction, canning, degassing and high temperature consolidation stage such as hot isostatic pressing (HIP) or extrusion. PM processed AMCs, contain oxide particles in the form of plate-like particles of few tens of nm thick and in volume fractions ranging from 0-05 to 0-5 vol% depending on powder history and processing conditions. These fine oxide particles tends to act as a dispersion-strengthening agent and often has strong influence on the matrix properties particularly during heat treatment [16].
Diffusion bonding:
Mono filament-reinforced AMCs are mainly produced by the diffusion bonding (foil-fibre-foil) route or by the evaporation of relatively thick layers of aluminum on the surface of the fibre. 6061 Al-boron fibre composites have been produced by diffusion bonding via the foil-fibre-foil process [17]. However, the process is more commonly used to produce Ti based fibre reinforced composites. The process is cumbersome and obtaining high fibre volume fraction and homogeneous fibre distribution is difficult. The process is not suitable to produce complex shapes and components.
2.6.2 Physical vapor deposition:
The process involves continuous passage of fibre through a region of high partial pressure of the metal to be deposited, where condensation takes place so as to produce a relatively thick coating on the fibre. The vapor is produced by directing a high power electron beam onto the end of a solid bar feed stock. Typical deposition rates are 5-10 um per minute. Composite fabrication is usually completed by assembling the coated fibres into a bundle or array and consolidating in a hot press or HIP operation. This technique can produced composites with uniform distribution of fibre and volume fraction as high as 80% [18].
2.6.3 Liquid metallurgy route
Liquid state processes include stir casting or compocasting, infiltration, spray casting and in situ (reactive) processing. The selection of the processing route depends on many factors including type and level of reinforcement loading and the degree of micro structural integrity desired.
Stir casting:
This involves incorporation of ceramic particulate into liquid aluminum melt and allowing the mixture to solidify. Here, the crucial thing is to create good wetting between the particulate reinforcement and the liquid aluminum alloy melt. The simplest and most commercially used technique is known as vortex technique or stir-casting technique. The vortex technique involves the introduction of pretreated ceramic particles into the vortex of molten alloy created by the rotating impeller. Lloyd (1999) has reports that vortex-mixing technique for the preparation of ceramic particle dispersed aluminum matrix composites was originally developed by Surappa & Rohatgi (1981) [19] at the Indian Institute of Science, Bangalore. Subsequently several aluminum companies further refined and modified the process which are currently employed to manufacture a variety of aluminum metal matrix composites on commercial scale [20].
The vortex method is one of the better known approaches used to create and maintain a good distribution of the reinforcement material in the matrix alloy. In this method, after the matrix material is melted, it is stirred vigorously to form a vortex at the surface of the melt, and the reinforcement material is then introduced at the side of the vortex. The stirring is continued for a few minutes before the slurry is cast. There are different designs of mechanical stirrers. Among them, the turbine stirrer is quite popular. During stir casting for the synthesis of composites, stirring helps in two ways: (a) transferring particles into the liquid metal, and (b) maintaining the particles in a state of suspension.
Micro structural inhomogeneities can cause notably particle agglomeration and sedimentation in the melt and subsequently during solidification. Inhomogeneity in reinforcement distribution in these cast composites could also be a problem as a result of interaction between suspended ceramic particles and moving solid-liquid interface during solidification. Generally it is possible to incorporate up to 30% ceramic particles in the size range 5 to 100 um in a variety of molten aluminum alloys .The process is not suitable for the incorporation of sub-micron size ceramic particles or whiskers. Another variant of stir casting process is compocasting. Here, ceramic particles are incorporated into the alloy in the semi solid state.
Infiltration process:
Liquid metal is injected into the interstices of the porous preforms of continuous fibre/short fibre or whisker or particle to produce MMCs. Depending on the nature of reinforcement and its volume fraction preform can be infiltrated, with or without the application of pressure or vacuum. MMCs having reinforcement volume fraction ranging from 10 to 70% can be produced using a variety of infiltration techniques. In order for the preform to retain its integrity and shape, it is often necessary to use silica and alumina based mixtures as binder. Some level of porosity and local variations in the volume fractions of the reinforcement are often noticed in the MMCs processed by infiltration technique. The process is widely used to produce aluminum matrix composites having particle/whisker/short fibre/continuous fibre as reinforcement.
In most of the cases the fibres do not act as preferential crystal nucleation sites during melt solidification .One consequences of this is that the last liquid to freeze , which is normally solute enriched, tend to locate around the fibres[21].
Spray deposition:
Spray deposition techniques fall into two distinct classes, depending whether the droplet stream is produced from a molten bath (Osprey process) or by continuous feeding of cold metal into a zone of rapid heat injection (thermal spray process). The spray process has been extensively explored for the production of MMCs by injecting ceramic particle/whisker/short fibre into the spray. MMCs produced in this way often exhibit inhomogeneous distribution of ceramic particles. Porosity in the as sprayed state is typically about 5-10%. Depositions of this type are typically consolidated to full density by subsequent processing. Spray process also permit the production of continuous fibre reinforced aluminum matrix composites. For this, fibres are wrapped around a mandrel with controlled inter fibre spacing, and the matrix metal is sprayed onto the fibres. A composite mono type is thus formed; bulk composites are formed by hot pressing of composite mono types. Fibre volume fraction and distribution is controlled by adjusting the fibre spacing and the number of fibre layers. MMCs processed by spray deposition technique are relatively inexpensive with cost that is usually intermediate between stir cast and PM processes. In-situ processing (reactive processing):
There are several different processes that would fall under this category including liquid-gas, liquid-solid, liquid-liquid and mixed salt reactions. In these processes refractory reinforcement are created in the aluminium alloy matrix. One of the examples is directional oxidation of aluminium also known as DIMOX process. In this process the alloy of Al-Mg is placed on the top of ceramic preform in a crucible. The entire assembly is heated to a suitable temperature in the atmosphere of free flowing nitrogen bearing gas mixture. Al-Mg alloy soon after melting infiltrates into the preform and composite is formed. Martin-Marietta's exothermic dispersion process or the XDTm process is another in-situ technique for composite processing. XDTm process is used to produce TiB2 reinforced aluminium matrix composites. The process is flexible and permits formation of both hard and soft phases of various sizes and morphologies that includes whiskers, particles and platelets in aluminium alloy matrices.
Gas-liquid reaction is also utilized to produce TiC reinforced aluminium matrix composites. For example, by bubbling carbonaceous gas like methane into Al-Ti melt kept at elevated temperature it is possible to produce Al-TiCp composites [22]. London and Scandinavian Metallurgical Company has developed an in-situ technique, which utilities reaction between mixed salts to produce a dispersion of fine TiB2 particles in an aluminium matrix. A major limitation of in-situ technique is related to the thermodynamic restrictions on the composition and nature of the reinforcement phase that can form in a given system, and the kinetic restrictions on the shape, size and volume fraction of the reinforcement that can be achieved through chemical reactions under a given set of test conditions.
2.7 Role of magnesium in cast aluminium alloy matrix composites
Wettabilty is a most significant problem when producing cast metal matrix composites. Particle -matrix interface have important effect on the mechanical properties of the composites, as good bonding promote load transfer to the higher strength ceramic particles .On the other hands, extensive inter facial reactions may deteriorate the mechanical properties of the composites. B. C. Pai et al. [23] reported that magnesium played an important role during the synthesis of aluminum alloy matrix composites with dis-persoids such as zircon (ZrSiO4), zirconia (ZrO2), titania (TiO2), silica (SiO2), graphite, alurninium oxide (Al203) and silicon carbide (SiC). Magnesium is one of the important alloying elements in aluminium. In A1-Si casting alloys Mg2Si is the key phase for alloy strengthening. Magnesium addition to aluminium reduces its casting fluidity at the same time as it reduces the surface tension of the aluminium sharply [24].
The presence of magnesium in aluminium alloy matrix during composite fabrication not only strengthens the matrix but also scavenges the oxygen from the surface of the dis-persoid, leading to an increase in the surface energy, of the dis-persoids. It can reduce Al2O3, either to form A1, MgA1204 or MgO depending upon its concentration. Hence there are three important role of magnesium in alumiunm melt.
Increasing the surface energies of the ceramics
Decreasing the surface tension of the liquid matrix alloy
Decreasing the solid/liquid interracial energy at the dispersoid matrix interface.

2.8 Particulate reinforced metal matrix composites
The other tendency in the research of Al matrix composites is to develop more inexpensive production techniques especially for discontinuously reinforced MMCs. The large consumption of monolithic aluminium alloys has enabled the development of production technology to very efficient and reliable level. Many of these technologies can be applied to production of aluminium matrix composites as well. For instance, standard shaping methods, such as extrusion, forging and rolling, can be used. Traditionally, liquid state processes [25¬26, 6], such as various casting methods, and powder metallurgical methods are used in production of particulate reinforced Al matrix composites. However, new deposition and in situ processes are potentially very efficient and economical and, therefore, they are actively studied. Powder metallurgical route is difficult to be automated and, thus it is very probably not the right answer for economical production of A1 matrix composites. Hence, the most promising processes are found among on the liquid state, deposition and in situ processes. The most simple, inexpensive and widely used methods for monolithic Al parts are various casting techniques. It is therefore natural that a lot of emphasize is put on developing these techniques for Al matrix composites as well. In order to ensure homogenizes distribution of reinforcement particles in the matrix metal stirring my using mechanical, electromagnetic or gas mixing is necessary. Especially, semi-solid slurry mixing methods, such as compocasting or rheocasting [27], have gathered increasing interest. Because of the high viscosity of the slurry higher volume fractions of reinforcement can be processed than in normal casting and the particles are more homogeneously distributed as well. It is even possible to use non-wetting particles, which are entrapped in the slurry. Moreover, the reactions between the matrix and reinforcements are reduced.
The SiC particles are the most common discontinuous reinforcements in Al matrix
composites although the density of SiC is slightly higher than that of Al. This is because it is
inexpensive and readily available but still gives the composite high strength and elastic
modulus. The improved wear resistance is often the primary feature as well. In the same way
as in the case of continuous SiC fibres the possibility of chemical reactions limits the high
temperature applications and may cause problems in production. Excess Si reduces the
reactivity of SiC in A1 remarkably. Another widely used particulate reinforcement in Al
matrix composites is Al203. In comparison to SiC it is much more inert in Al and it is also
oxidation resistant. Accordingly, it is much more suitable for high temperature fabrication and
use. In order to overcome the problem of poor wettability of A1203 by A1, which disturbs
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especially the liquid stirring production routes, the matrix is alloyed or the reinforcement is surface coated. As described previously, Li is found to be a beneficial alloying element. MgO on the surfaces of A1203 is also improving the wettability. On the other hand, in squeeze casting the wettability is not as large problem as in liquid stirring. Therefore, this efficient technique has been often utilized in production of particulate A1203 reinforced Al matrix composites. In fact, this combination of production method and composite material Al is currently the most promising candidate for large scale production of relatively inexpensive MMCs for general Al applications. In the early stage of development of the cast particulate composite, the particles are injected in molten Al through carrier gas[28], to achieve greater recovery, the coating of the particles has been suggested than the uncoated one e.g. Nickel coating with graphite particles in case of Al matrix composites. Ni improves the wettability of the particle by Al melt. Not only Ni but also the addition of Mg, Li, Si Ca, in Al melt improves wettabi1ity either by changing the interface energy through some interracial reaction or by modifying the oxide layers in the metal surface Detailed investigation of Pai et al. and P.K.Rohatgi [6] and co workers have observed that magnesium increases the wettability of the fly ash in the Al melt. In a recent study it has been demonstrated that the addition of Ca improves the wettability of Al 4.5% eu melt by its effects on improvement of retention of particles is less that with Mg addition. To ensure the uniform distribution of particles, stirring of the melt are suggested.
To ensure the uniform distribution of particles, stirring of the melt are suggested. Pellet methods are developed to incorporate ceramic particles into Al melt by Pai and Mc Donald and co workers [29, 30]. In this method the coarser particles of base alloy and reinforcing ceramic particles are mixed and pressed to form pellets. These pellets were subsequently plunged into the melt followed by slow stirring manually or mechanically. But the distribution of particles of the cast particulate composite was not satisfactory uniform when it is prepared by injection technique or pallet method without stirring. To over come such difficulty Vortex method was developed [19, 31]. This the most common method used at present for cast metal matrix particulate composite. In this method molten metal in a crucible is stirred with a available impeller to form a vortex in the melt. Required amount of ceramic particles are added into the vortex at a predetermined rate. The particles get entrapped in the melt and distribute uniformly in it during stirring. The development of SiO2 coating on fly ash particles is demonstrated as an effective way to improve matrix-reinforcement bonding during the manufacturing by a liquid route of Al matrix composite [32].
Heat treatment of the particles before dispersion into the melt aids their transfer by causing desorption of adsorbed gases from the particle surface. Heating silicon carbide particles to 9008C, for example, assists in removing surface impurities and in the desorption of gases, and alters the surface composition by forming an oxide layer on the surface[33].The addition of pre-heated alumina particles in Al-Mg melt has been found to improve the wetting of alumina [34]. A clean surface provides a better opportunity for melt-particles interaction, and thus, enhances wetting. Ultrasonic techniques, various etching techniques, and heating in a suitable atmosphere can be used to clean the particle surface. Ultrasonic vibration has been applied to molten aluminium in order to improve the wettability of alumina particles [35]. S. Sarkar and S. C. panigrahi have worked on the Effect of Particle Distribution on the properties of Aluminum Matrix In-situ Particulate Composites [36] and conclude that discontinuously reinforced aluminum matrix composites are fast emerging materials that compete with conventional metallic materials. In-situ particulate composites in comparison with conventional cast particulate composites produced by external addition, promote cleaner interfaces, eliminate interface incompatibility of the matrices with the reinforcements, help to achieve greater thermodynamic stability of reinforcement particles in the matrix at elevated temperature, and also increase the possibility of developing coherency between the matrix and particles formed in-situ. The morphology and the distribution of particles strongly influence the physical and mechanical properties of the composites. In the present study, illuminate was added to molten aluminum, aluminum-magnesium and aluminum-silicon alloys by vortex method. The oxides present in ilumenite are observed to react with aluminum, magnesium and resulting in production of Al2O3, MgO and metallic Fe and Ti, which dissolved in liquid aluminum. The strength and hardness value showed considerable improvement. The resulting composites also show appreciable ductility
2.9 Aluminium -fly ash particulate reinforced composite
M. Ramachandra K. Radhakrishna [37] has worked on the Effect of reinforcement of fly ash on sliding wear, slurry erosive wear and corrosive behavior of aluminium matrix composite. Al (12 wt% Si) as matrix material and up to 15 wt% of fly ash particulate composite was fabricated using the stir casting rote and came forward into following conclusions
Fly ash improves abrasive wear resistance (20-30%) of Al. and reduces the coefficient
of friction.
Increase in normal load and sliding velocity increases magnitude of wear and frictional force.
Different wear mechanisms were studied under varying different parameter such as normal load, % of fly ash content and sliding velocity. Four different mechanisms are found that are abrasion, oxidation, delamination, thermal softening and adhesion. Corrosion resistance of reinforced composite has decreased with increase in flyash content.
Sudarshan, M.K. Surappa [38, 39] have synthesized A356 Al-fly ash particle composites .They studied mechanical properties and dry sliding wear and come into brief idea that
¢ Fly ash with narrow size range (53-106um) show better properties compared with the wider size range (0.5-400um) particles.
¢ The damping capacity of composite increases with the increase in volume fraction of fly ash.
¢ Fracture surface of composites show mixed mode (ductile and brittle) fracture.
¢ The 6% of fly ash particles into A356 Al alloy shows low wear rates at low loads (10 and 20 N) while 12% of fly ash reinforced composites show lower wear rates compared to the unreinforced alloy in the load range 20-80 N.
¢ The types of wear dominant in unreinforced alloy are adhesive wear, whereas abrasive wear is predominant in composites. At higher load, subsurface delamination is the main mechanism in both the alloy as well in composites.
R.Q. Guoa and P.K. Rohatgi, while studding the changes of chemical reaction between the Al and the fly ash during synthesis or reheating [40] of fly ash found out that
¢ The chemical reactions do occur between the fly ash an Al melts. The SiO2and Fe2O3 present in the fly ash is reduced to Si and Fe .The melt oxidized to Al2O3.
The above mentioned reactions do occur rapidly at the temperature more than 8500C
.At this higher temperature the free energy of transformation has significant negative
value to occur this reaction spontaneously.
The reaction between Al and fly ash complete after10 hours P. K. Rohatgia, J. K. Kima, [41] and co workers have worked on Compressive characteristics of A356/fly ash cenosphere composites synthesized by pressure infiltration technique and conlude that
¢ Using gas pressure infiltration up to 20 to 65% volume percentage of fly ash can be reinforced.
¢ The various factors affecting the densities of the composites melt temperature, applied pressure, and the size of particles.
P. K. Rohatgi, N. Gupta, and Somon Alaraj [42] have studied the coefficient of thermal expansion of pure Al containing 65 vol% of hollow fly ash particles and suggested that
Composites with a lower coefficient of thermal expansion can be made by incorporating cenospheres under controlling the processing parameter for a given volume fraction of reinforcement.
Composite synthesized at different pressure for different infiltration time (min) and came to conclude tha increase in the infiltration pressure and temperature improves the infiltration and decreases the entrapped air voids, as a result of which lower the coefficient of thermal expansion. J. Sobczak, J. Bienias and co workers [43] have synthesized fly ash particles as reinforcement in metal matrix composites by squeeze casting technology and gravity casting and compared between them and have come to following conclusion
Squeeze casting technology is much useful in comparison with gravity casting. Because it has structural homogeneity with less porosity and good interracial bonding. Due to presence of fly ash particle in the composite the corrosion is pitting type corrosion.
S. Sarkar, S. sen and S. C. Mishra and co workers has studied on Aluminum - fly ash composite produced by impeller mixing[7] and came into a brief idea that
¢ Up to 17wt% fly ash reinforcement can be reinforced by liquid metallurgy route.
The addition of magnesium into the alumium melt increase the wettabilty and thus increase in the mechanical properties such as hardness, tensile strength and the wear resistance is observed.
P.K. Rohatgi, D. Weiss, and Nikhil Gupta [44] in this paper studied that al- fly composite can be used for automotive and other applications and show details on environmental and energy benefits.
The potential cost, energy, and pollution savings as a result of incorporation of fly ash in aluminum is huge.
The potential reduction in cost and energy content of individual auto parts, energy consumption, and emissions due to the replacement of 20% aluminum by fly ash show the substantial benefit of using ALFA composites.
2.10 FLY ASH
Fly ash is one of the residues generated in the combustion of coal. It is an industrial byproduct recovered from the flue gas of coal burning electric power plants. Depending upon the source and makeup of the coal being burned, the components of the fly ash produced vary considerably, but all fly ash includes substantial amounts of silica (silicon dioxide, SiC2) (both amorphous and crystalline) and lime (calcium oxide, CaC). In general, fly ash consists of SiC2, Al2C3, and Fe2C3 as major constituents and oxides of Mg, Ca, Na, K etc. as minor constituent. Fly ash particles are mostly spherical in shape and range from less than 1 um to 100 um with a specific surface area, typically between 250 and 600m2/kg. The specific gravity of fly ash vary in the range of 0.6-2.8 gm/cc. Coal fly ash has many uses including as a cement additive, in masonry blocks, as a concrete admixture, as a material in lightweight alloys, as a concrete aggregate, in flow able fill materials, in roadway/runway construction, in structural fill materials, as roofing granules, and in grouting. The largest application of fly ash is in the cement and concrete industry, though, creative new uses for fly ash are being actively sought like use of fly ash for the fabrication of MMCs.
2.10.1Classification on the basis of Chemical Composition:
Fly ash is a pozzolanic material and has been classified into two classes, F and C, based on the chemical composition of the fly ash. According to ASTM C 618, the chemical requirements to classify any fly ash are shown in Table 2.10.1.
Table 2.10.1Chemical Requirements for Fly Ash Classification
Properties Class F Class C
Silicon dioxide (SiC2) plus aluminum oxide (Al2C3) plus iron oxide (Fe2C3), min, % 70.0 50.0
Sulfur trioxide (SC3), max, % 5.0 5.0
Moisture Content, max, % 3.0 3.0
Loss on ignition, max, % 6.0* 6.0
2.11.2 On basis of size, shape and structure:
1. Precipitator fly ash
It is spherical in nature, the spheres are solid and the density is in the range of 2.0 -2.5 g cm-3. 2. Cenosphere fly ash
It is also spherical in shape but these spheres are hollow, so the density of this kind of fly ash is very less as compared to the precipitator fly ash. Here density is less than 1 gm cm-3 (0.3-0.6gm/cc)
2.11 WHY FLY ASH
1. The preference to use fly ash as a filler or reinforcement in metal and polymer matrices is that fly ash is a byproduct of coal combustion, available in very large quantities at very low costs since much of this is currently land filled. Currently, the use of manufactured glass micro spheres has limited applications due mainly to their high cost of production. Therefore, the material costs of composites can be reduced significantly by incorporating fly ash into the matrices of polymers and metallic alloys. However, very little information is available on to aid in the design of composite materials, even though attempts have been made to incorporate fly ash in both polymer and metal matrices. Cenosphere fly ash has a lower density than talc and calcium carbonate, but slightly higher than hollow glass. The cost of cenosphere is likely to be much lower than hollow glass .Cenosphere may turn out to be one of the lowest cost fillers in terms of the cost per volume.
2. The high electrical resistivity, low thermal conductivity and low density of fly-ash may be helpful for making a light weight insulating composites.
3. Fly ash as a filler in Al casting reduces cost, decreases density and increase hardness, stiffness, wear and abrasion resistance. It also improves the maintainability, damping capacity, coefficient of friction etc. which are needed in various industries like automotive etc.
4. As the production of Al is reduced by the utilization of fly ash. This reduces the generation of green house gases as they are produced during the bauxite processing and alumina reduction.
2.12Chemical reaction between al and fly ash
The thermodynamic analysis indicates that there is possibility between the reaction of Al melt and the fly ash particles. The particles contain alumina, silica and iron oxide which during solidification process of Al fly ash composites or during holding such composites at temperature above 8500 C, are likely to undergo chemical reactions, reported by P.K.Rohatagi and Guo. The experiments indicate that there is a progressive reduction between SiC2, Fe2C3 and mullite by Al and formation of Al2C3, Fe and Si. The wall of cenosphere fly ash particles progressive disintegrates into discrete particles into the reaction progress.
2.13 Wear behavior
Wear behavior is the surface damage or removal of material from one or both of two solid surfaces in a sliding, rolling, or impact motions relative to one another. So it is surface phenomenon that occurs by displacements and detachments of materials. Wear problems generally differ from those entailing outright breakage, as wear usually a progressive loss of weight and alterations of dimensions over a periods of time.
Wear is undesirable products in almost all machine applications such as bearings seals gears, and cams etc. Wear of those components may range forms mild polishing type attrition to rapid and severe removal of material accommodating with surface roughing. W heather or not wear constitutes failure of these components depends upon whether the wear deleteriously affects the ability of the components to function. Even mild polishing type ear of a close fitting pool in a hydraulic vale may cause excessive leakage and thus constitute failure, even though the surface of the pool is smooth and apparently undamaged .On the other hand, a hammer in rock crusher can continue to function satisfactorily in spite of serve detecting, gouging and removal of as much as several inches of surface metal. Laws of wear
The laws governing wear are not completely clear but both adhesive and abrasive wear a simple equation can be written as:
V/X = K*(W/H)
Where,
V=Wear volume X=Sliding distance W=Normal load applied
H=Initial hardness of the softer sliding components K= Wear coefficients
Further it has also been shown that there is relation between hardness H of the metal and its yield or flow pressure oy which given by:
H= 3* Oy
From these equations we can conclude that the total volume of the metal removed due to sliding is directly proportional to applied loads, sliding distance and inversly proportional to hardness of the softer sliding component.

2.12.1Types of wear
Wear has been categorized in various ways. The phenomenological approach is based on a macroscopic description of appearance of the worn surface. For that is suffering, rubbing fitting. But his system has its limitations as it goes not focus on his mechanism of wear and therefore must relay almost entirely on imperial solutions to wear problems. Another way is to categorize wear ways on the fundamental mechanism that operating but this approach is complicated by the fact that more than one mechanism may be operating at a time and by the lack of sufficient information .A third type of classification describes wear based on the shape and size of the wear debris particles generated.
A potential wear situ tons exists whenever there is a relative motion between two solids under loads. Broadly speaking the motion can be unit directional or reciprocating either sliding or rolling .There may be a combination of rolling and sliding are wear may occur due to oscillatory movement at small amplitudes metal can interact with non metal or liquids such as lubricating or marine water.
Depending on the nature of movement of the media following types wear has been classified.
> Abrasive wear
> Adhesive wear
> Corrosion wear
> Erosive wear
> Fatigue wear
> Fretting Abrasive wear
Abrasive wear occurs when asperities of rough, hard surface or hard particles slide on a softer
surface and damage the interface by plastic deformation or fracture. In case of ductile
materials with high fracture toughness, hard asperities or hard particles result in the plastic
flow of the softer material. Most metallic and ceramic surfaces during sliding show clear
evidence of plastic flow, even some ceramic brittle materials. In one way abrasive wear is
classified as gouging abrasion, high stress (grinding) abrasion. In gouging, abrasion large
particles are removed from surface, leaving dip groves and/or pits .High stress or grinding
abrasion is accompanied by fracture of the abrasive particles. Low stress or scratching
abrasion occurs when the loads is low enough that the abrasive particles are not fracture.
Another way of classification divides abrasion into two bodies or three body abrasion. In the
first case the hard surface is the harder of two rubbing surface (two body abrasion), for
27
example, in mechanical operations such as grinding, cutting and machining. In three body abrasion; the hard surface is a third body generally a small particle of abrasive, caught between the two surfaces and sufficiently harder that is able to abrade either one or both mating surfaces, for examples, in free-abrasive lapping and polishing. Adhesive wear
Adhesive wear occurs when two nominally flat bodies are in sliding contact, whether lubricated or not. Adhesion (or bonding) occurs at the asperity contacts at the interface, and these contacts are shared by sliding which may result in detachment of a fragment from one surface and attachment to the other surface .As the sliding continues the transferred fragment may come off the surface on which they are transferred and be transferred back to original surface ,or else from loses wear particles .Some are fractured by fatigue process during repeated loading and unloading action resulting in the form of lose particles.
Corrosive wear
Wear where contribution to the wear rate by the chemical reaction with the environment .In certain cases chemical reaction is followed by removal of the corrosion product by mechanical action that is abrasion .It may be occur that the mechanical action precedes the chemical action and results in he formation of very small particles of debris, which subsequently react with environment. Due to the chemical reaction change the corrosion by reaction with environment.
Erosive wear
This type of wear results when grits impinge on solids while cavitations erosion may arise when a components rotates in a medium .Erosion of surface can take place in a liquid medium,even without the presence of solid abrasive in that medium. Cavitations involve formation and subsequent collision of bubbles within the liquids .The collision of liquid droplets with the solid surface at high speed results in form of liquid erosion called liquid impingement. It involves the progressive removal of materials from surfaces by repeated impulse loading at microscopically small areas. Fatigue wear
Fatigue wear arises as a result of cyclic loadings for examples in rolling elements bearings lose of materials occurs by spelling of surface layers .It may be due to failure of lubricated contacts as in gears, friction drives and ball and roller bearings. The fatigue cracks are believed starts below the surface at a point where the shear stress is maximum so improve the components .Working is done at low contacts loads and having an optimum depth of hard
cases coupled with a high degree of surface finish .
Fretting
Fretting occurs where low amplitude oscillatory motion in tangential direction takes place between contacting surfaces, which are nominally at rest. This is a common occurrence science most machinery is subjected to vibration, both in transit and in operation .Basically, fretting is a form of adhesive or abrasive wear where the normal load causes adhesion between asperities and oscillatory movement causes rupture resulting in wear debris. Fretting may be of two type; One is contact collision that takes place between the bore of bearings and the shaft or between the out side surface of bearing contact and bore housing. Another type is fretting damage within bearing contact area .This type of fretting is frequently reffed as false braining.
CHAPTER-3
3. EXPERIMENTAL WORK

3.1 Raw materials

The matrix material used in the experiment investigation was commercially pure aluminium.The fly ash was collected from RSP steel pant Orissa, India. The particle size of the fly as received condition lies in the range from (0.1-100 urn).

3.2 Melting and casting

The aluminum fly ash metal matrix composite was prepared by stir casting route. For this we took 500gm of commercially pure aluminum and desired amount of fly ash particles. The fly ash particle was preheated to 3000C for three hour to remove moisture. Commercially pure aluminum was melted in a resistance furnace. The melt temperature was raised up to 7200C and it was degassed by purging hexa chloroethane tablets. Then the melt was stirred with the help of a mild steel turbine stirrer. The stirring was maintained between 5 to 7 min at an impeller speed of 200 rpm .The melt temperature was maintained 7000C during addition of fly ash particles. The dispersion of fly ash particles were achieved by the vortex method. The melt with reinforced particulates were poured into the preheated permanent metalic mold. The pouring temperature was maintained at 6800C.The melt was then allow to solidify the moulds. The composites were made with a different amount of fly-ash (i.e.5, 10, 20, wt %),
Magnesium and silicon were added to increase the wettability of fly ash particles.
3.3 Microstructural characterization. 3.3.1 Scanning electron microscopy
Micro structural characterization studies were conducted on unreinforced and reinforced samples. This is accomplished by using scanning electron microscope. The composite samples were metallographically polished prior to examination. Characterization is done in etched conditions. Etching was accomplished using Keller's reagent. The SEM micrographs of composite and wear debris were obtained using the scanning electron microscope. The images were taken in both secondary electron (SE) and back scattered electron (BSE) mode according to requirement. Microscopic studies to examine the morphology, particle size and micro structure were done by a JEOL 6480 LV scanning electron microscope (SEM) equipped with an energy dispersive X-ray (EDX) detector of Oxford data reference system. Micrographs are taken at suitable accelerating voltages for the best possible resolution using the secondary electron imaging.

3.3.2 Optical microscopy
The casting procedure was examined under the optical microscope to determine the casr structure .A section was cut from the castings. It is first belt grinded followed by polishing with different grade of emery papers. Then they were washed and polished in clothes and then washed, dried and etched with Keller's solution and then examined though optical microscope.
3.4 Particle size analysis
Particle size of the milled powder was measured by Malvern particle size analyzer (Model Micro-P, range 0.05-550 micron). Firstly, the liquid dispersant containing 500 ml of distilled water was kept in the sample holder. Then the instrument was run keeping ultrasonic displacement at 10.00 micron and pump speed 1800 rpm.
3.4.1 Hardness
Bulk hardness measurements were carried out on the base metal and composite samples by using standard Brinnel hardness test. Brinnel hardness measurements were carried out in order to investigate the influence of particulate weight fraction on the matrix hardness. Load applied was 750kgs and indenter was a steel ball of 5 mm diameter.
3.4.1 Tensile test
The tensile testing of the composite was done, on Instron testing machine. The sam


CONTENTS
LIST OF FIGURES i
LIST OF TABLES ii
ABSTRACT IV
CHAPTER-1:
1.1 INTRODUCTION 1
CHAPTER-2:
2. LITERATURE SURVEY
2.1. Composite 3
2.2. Classifications of composites 4
2.3. Strengthening mechanism of composite 6
2.4. Interfacial bonding mechanism 8
2.5. Metal matrix composite 10
2.6. Fabrication techniques for metal matrix composites 11
2.7. Role of magnesium in cast aluminiurn alloy matrix composites 16
2.8. Particulate reinforced metal matrix composites 17
2.9. Aluminium -fly ash particulate reinforced composite 20
2.10. Fly ash 23
2.11. Why fly ash 24
2.12. Chemical reaction between al and fly ash 25
2.13. Wear behaviour 26
CHAPTER-3:
3. EXPERIMENTAL WORK
3.1 Raw materials 30
3.2 Melting and casting 30
3.3 Microstructural characterization 31
3.4 Particle size analysis 32
3.5 Mechanical properties observation 33
3.6 Sliding wear behavior 34
3.7 Worn surface and debris examination 34
CHAPTER-4
4. RSEULTS AND DISCUSSION
4.1 fly ash analysis 35
4.2 Optical microstructure of cast composite 37
4.3 SEM micrographs of the MMCs 39
4.4 Distribution of particles in MMCs 41
4.5 Mechanical properties determination 43
4.6 Wear behavior 45
4.7 Frictional characteristics 49
4.8 Microscopic examination 50
4.9 SEM micrographs of worn surface of the composite 53
4.10 Wear debris 54
4.11 Fractograph of the selected composite 56
CHAPTER-5:
CONCLUSION 57
CHAPTER-6:
REFERENCES
58
LIST OF FIGURES
2.1. Schematic diagram showing the contact angle
that describes wettability 8
3.1. Laboratory stir casting set up 31
3.2: JEOL JSM-6480LV scanning electron microscop 32
3.3: Malvern particle size analyzer
(Model Micro-P, range 0.05-550 micron) 33
4.1 SEM Micrograph of fly ash used in the study 35
4.2. Particle size analysis of fly ash 36 Optical micrographs of MMCs
4.3. Al+ 5% fly ash composite 37
4.4. Al+ 10% fly ash composite 37
4.5. Al+15% fly ash composite 37
4.6. Al+20% fly ash composite 37
4.7. Al+2%Si+10% fly ash composite 38
4.8. Al+2%Mg+10% fly ash composite 38 SEM micrographs of MMCs
4.9. Al+ 5% fly ash composite 39
4.10. Al+ 10% fly ash composite 39
4.11. Al+15% fly ash composite 39
4.12. Al+ 20% fly ash composite 39
4.13. Al+2%Si+10% fly ash composite 40
4.14. Al+2%Mg+10% fly ash composite 40
4.15. Macrographs showing distribution of particles 41
4.16. Graph showing variation in hardness with
composition of MMCs 43
4.17-Wear behavior of MMCs with different
composition under normal load of 10N 45
4.18-.Wear behavior of MMCs with different
composition under normal load of 15N 46
4.19-Wear behavior of MMCs with different
composition under normal load of 20N 47
4.20- Wear behavior of MMCs with variation in normal load 47
4.21- Variation of behavior of MMCs with variation
in sliding velocity 48
4.22- Variation of coefficient of friction with
composition of the composite 49
4.23-Grooves and scratch marks indicating abrasion wear 50
4.24- Deep smooth and large grooves under higher loads 50
4.25- Wear debris filling the valleys in the wear surface 51
4.26- Delamination of wear surface under a loadof 20N 52 4.27”SEM micrographs of the worn surfaces after the wear test under velocity 1 m/s; time 30min; (a) load 10N and (b) 20N. 53 4.28-SEM micrographs of debris of the MMCs at different loads at (a) 10N, (b)
15Nan© 20N 54
4.29-SEM fractograph of Al+2%Mg+10%fly ash 56
LIST OF TABLES
2.10. Chemical Requirements for Fly Ash Classification 23
4.1. Chemical composition of fly ash 35
4.2. BHN values of the samples 43
4.3. Tensile prope