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Upon being mechanically stressed, a material will, in general, exhibit the following sequence of responses: elastic deformation, plastic deformation, and fracture. This chapter addresses the second response: plastic deformation. A sound knowledge of plasticity is of great importance for the following reasons.
Many projects are executed in which small plastic deformations of the structure are accepted. The “theory of limit design” is used in applications where the weight factor is critical, such as space vehicles and rockets. The rationale for accepting a limited plastic deformation is that the material will work-harden at that region, and plastic deformation will cease once the flow stress (due to work-hardening) reaches the applied stress.
It is very important to know the stresses and strains involved in deformation processing, such as rolling, forging, extrusion, drawing, and so on. All these processes involve substantial plastic deformation, and the response of the material will depend on its plastic behavior during the processes. The application of plasticity theory to such processes is presented later in this chapter.
The mechanism of fracture can involve plastic deformation at the tip of a crack. The way in which the high stresses that develop at the crack can be accommodated by the surrounding material is of utmost importance in the propagation of the crack. A material in which plastic deformation can take place at the crack is “tough,” while one in which there is no such deformation is “brittle.”
The separation or fragmentation of a solid body into two or more parts, under the action of stresses, is called fracture. The subject of fracture is vast and involves disciplines as diverse as solid-state physics, materials science, and continuum mechanics. Fracture of a material by cracking can occur in many ways, principally the following:
Slow application of external loads.
Rapid application of external loads (impact).
Cyclic or repeated loading (fatigue).
Time-dependent deformation (creep).
Internal stresses, such as thermal stresses caused by anistropy of the thermal expansion coefficient or temperature differences in a body.
The process of fracture can, in most cases, be subdivided into the following categories:
Damage accumulation.
Nucleation of one or more cracks or voids.
Growth of cracks or voids. (This may involve a coalescence of the cracks or voids.)
Damage accumulation is associated with the properties of a material, such as its atomic structure, crystal lattice, grain boundaries, and prior loading history. When the local strength or ductility is exceeded, a crack (two free surfaces) is formed. On continued loading, the crack propagates through the section until complete rupture occurs. Linear elastic fracture mechanics (LEFM) applies the theory of linear elasticity to the phenomenon of fracture – mainly, the propagation of cracks. If we define the fracture toughness of a material as its resistance to crack propagation, then we can use LEFM to provide us with a quantitative measure of fracture toughness.
Environment by its omnipresence, except perhaps in space, affects the behavior of all materials. Such effects can range from swelling in polymers to surface oxidation of metals and nonoxide ceramics to catastrophic failure of some materials under a combined action of stress and environment. Environmental degradation of materials is often referred to as corrosion. Such damage is generally time-dependent, i.e., one is able to predict it. Over time, however, envir-onmental damage can become critical. There is, however, a more insidious corrosion problem which is time-independent. Examples of time-independent corrosion include stress corrosion cracking (SCC), environment induced embrittlement, etc. Such damage can occur at anytime, without much warning. There are many examples of such failures resulting in human and economic loss. Corrosion of structural components in aging aircraft is a serious problem. Just to cite one such example, a Boeing 737 belonging to Aloha Airlines, which flew inter island in Hawaii, lost a large portion of its upper fuselage at 7,500 m (24,000 feet) in the air. It turned out that the fuselage panels joined by rivets had corroded, which resulted in the mid-flight failure due to corrosion fatigue.
All materials (metals, ceramics, and polymers) show phenomena of premature failure or mechanical property degradation under certain combinations of stress and environment. We describe below the salient points in regard to environmental effects in different materials. We emphasize the role that the microstructure of a given mater-ial plays in this phenomenon, especially in environmentally assisted fracture.
Courses in the mechanical behavior of materials are standard in both mechanical engineering and materials science/engineering curricula. These courses are taught, usually, at the junior or senior level. This book provides an introductory treatment of the mechanical behavior of materials with a balanced mechanics–materials approach, which makes it suitable for both mechanical and materials engineering students. The book covers metals, polymers, ceramics, and composites and contains more than sufficient information for a one-semester course. It therefore enables the instructor to choose the path most appropriate to the class level (junior- or senior-level undergraduate) and background (mechanical or materials engineering). The book is organized into 15 chapters, each corresponding, approximately, to one week of lectures. It is often the case that several theories have been developed to explain specific effects; this book presents only the principal ideas. At the undergraduate level the simple aspects should be emphasized, whereas graduate courses should introduce the different viewpoints to the students. Thus, we have often ignored active and important areas of research. Chapter 1 contains introductory information on materials that students with a previous course in the properties of materials should be familiar with. In addition, it enables those students unfamiliar with materials to “get up to speed.” The section on the theoretical strength of a crystal should be covered by all students. Chapter 2, on elasticity and viscoelasticity, contains an elementary treatment, tailored to the needs of undergraduate students.
In Chapter 7, we described the macroscopic aspects of the fracture behavior of materials. As with other characteristics, the microstructure of a material has a great influence on its fracture behavior. In what follows, we present a brief description of the microstructural aspects of crack nucleation and propagation, as well as the effect of the environment on the fracture behavior of different materials. Figure 8.1 shows, schematically, some important fracture modes in a variety of materials. These different modes will be analyzed in some detail in this chapter. Metals fail by two broad classes of mechanisms: ductile and brittle failure.
Ductile failure occurs by (a) the nucleation, growth, and coalescence of voids, (b) continuous reduction in the metal's cross-sectional area until it is equal to zero, or (c) shearing along a plane of maximum shear. Ductile failure by void nucleation and growth usually starts at second-phase particles. If these particles are spread throughout the interiors of the grains, the fracture will be transgranular (or transcrystalline). If these voids are located preferentially at grain boundaries, fracture will occur in an intergranular (or intercrystalline) mode. The appearance of a ductile fracture, at high magnification (500× or higher) is of a surface with indentations, as if marked by an ice-cream scooper. This surface morphology is appropriately called dimpled. Rupture by total necking is very rare, because most metals contain second-phase particles that act as initiation sites for voids.
The second edition of Mechanical Behavior of Materials has revised and updated material in every chapter to reflect the changes occurring in the field. In view of the increasing importance of bioengineering, a special emphasis is given to the mechanical behavior of biologi-cal materials and biomaterials throughout this second edition. A new chapter on environmental effects has been added. Professors Fine and Voorhees make a cogent case for integrating biological materials into materials science and engineering curricula. This trend is already in progress at many US and European universities. Our second edition takes due recognition of this important trend. We have resisted the temptation to make a separate chapter on biological and biomaterials. Instead, we treat these materials together with traditional materials, viz., metals, ceramics, polymers, etc. In addition, taking due cognizance of the importance of electronic materials, we have emphasized the distinctive features of these materials from a mechanical behavior point of view.
The underlying theme in the second edition is the same as in the first edition. The text connects the fundamental mechanisms to the wide range of mechanical properties of different materials under a variety of environments. This book is unique in that it presents, in a unified manner, important principles involved in the mechanical behavior of different materials: metals, polymers, ceramics, composites, electronic materials, and biomaterials. The unifying thread running throughout is that the nano/microstructure of a material controls its mechanical behavior. A wealth of micrographs and line diagrams are provided to clarify the concepts.
In this chapter, we discuss one important means of altering the mechanical response of metals and ceramics: martensitic transformation. Martensitic transformation is a highly effective means of increasing the strength of steel. An annealed medium-carbon steel (such as AISI 1040) has a strength of approximately 100 MPa. By quenching (and producing martensite), the strength may be made to reach about 1 GPa, a tenfold increase. The ductility of the steel is, alas, decreased.
A quite different effect is observed in ceramics. Martensitic transformation can be exploited to enhance the toughness of some ceramics. If a ceramic undergoes a martensitic transformation during the application of a mechanical load, the propagation of cracks is inhibited. For example, partially stabilized zirconia has a fracture toughness of approximately 7 MPa m1/2. An equivalent ceramic not undergoing martensitic transformation would have a toughness less than or equal to 3 MPa m1/2.
An additional, and very important, effect associated with martensitic transformations is the “shape-memory effect.” Alloys undergoing this effect “remember” their shape prior to deformation. The three effects just described have important technological applications.
Structures and Morphologies of Martensite
Quenching has been known for over 3,000 years and is, up to this day, the single most effective mechanism known for strengthening steel. However, it is only fairly recently that the underlying mechanism has been studied in a scientific manner and understood.
There is some confusion in the literature about the terminology pertaining to fatigue. We define fatigue as a degradation of mechanical properties leading to failure of a material or a component under cyclic loading. This definition excludes the so-called phenomenon of static fatigue, which is sometimes used to describe stress corrosion cracking in glasses and ceramics in the presence of moisture. Brittle solids (glasses and crystalline ceramics) undergo subcritical crack growth in an aggressive environment under static loads. Silica-based glasses are especially susceptible to this kind of crack growth in the presence of moisture. If a glassy phase exists at grain boundaries and interfaces, it will be susceptible to such an attack. Thus, static fatigue is more appropriately a stress corrosion phenomenon, rather than a cyclic stress-related phenomenon.
In general, fatigue is a problem that affects any structural component or part that moves. Automobiles on roads, aircraft (principally the wings) in the air, ships on the high sea constantly battered by waves, nuclear reactors and turbines under cyclic temperature conditions (i.e., cyclic thermal stresses), and many other components in motion are examples in which the fatigue behavior of a material assumes a singular importance. It is estimated that 90% of service failures of metallic components that undergo movement of one form or another can be attributed to fatigue. Often, a fatigue fracture surface will show some easily identifiable macroscopic features, such as beach markings.
This study examines the size-dependent deformation response of pure LiF single crystals using microcompression testing. Microcrystals with an 〈001〉 orientation and sample diameter D ranging from 1 to 20 μm were fabricated by focused ion beam (FIB)-milling from bulk crystals having a low initial dislocation density. Both as-grown and γ-irradiated crystals were examined to characterize the effect of an increased point defect density on the size-affected plastic flow response. Similar to previously studied face-centered cubic (FCC)-derivative metals, both types of LiF microcrystals exhibit typical size-dependent plastic flow behavior: a dramatic size-dependent and statistically varying flow stress, atypically high strain hardening rates at small plastic strains, and fast intermittent strain bursts. The size-dependent strengthening obeys a power law, σ ∼ D−m, where m ≈ 0.8, and this rapid hardening results in engineering flow stresses of 650 MPa in 1-μm samples. The findings are evaluated against possible dislocation mechanisms that could be responsible for the observed size effects.
Using an infrared camera, the temperature evolution of as-cast and relaxed bulk metallic glasses during compression was measured. Substantial variations in the temperatures of both glasses during plastic deformation were observed, which are conjectured to result at least partially from shear-banding phenomena. The relaxed glass has a larger temperature rise than the as-cast glass, which can be attributed to a reduction in the free volume. The larger temperature increase in the relaxed glass may be responsible for the observed work softening. The relaxed glass also has a higher maximum temperature than the as-cast, which can be attributed to a stronger strain-rate dependence of the temperature rise rate, and a shorter dissipation time scale for the heat due to conduction. The experimental data follow the well-known model behavior, and suggest the possibility of a statistical correlation between the fluctuations of strain rates and the rates of the temperature variation.
Microstructure and hardness evolution of arc-evaporated single-phase cubic Al0.56Cr0.44N and Al0.68Cr0.32N coatings have been investigated after thermal treatment in Ar atmosphere. Based on a combination of differential scanning calorimetry and x-ray diffraction studies, we can conclude that Al0.56Cr0.44N undergoes only small structural changes without any decomposition for annealing temperatures Ta ⩽ 900 °C. Consequently, the hardness decreases only marginally from the as-deposited value of 30.0 ± 1.1 GPa to 29.4 ± 0.9 GPa with Ta increasing to 900 °C, respectively. The film with higher Al content (Al0.68Cr0.32N) exhibits formation of hexagonal (h) AlN at Ta ⩾ 700 °C, which occurs preferably at grain boundaries as identified by analytical transmission electron microscopy. Hence, the hardness increases from the as-deposited value of 30.1 ± 1.3 GPa to 31.6 ± 1.4 GPa with Ta = 725 °C. At higher temperatures, where the size and volume fraction of the h-AlN phase increases, the hardness decreases to 27.5 ± 1.0 GPa with Ta = 900 °C.
In this article, we review current research efforts to control the magnetic behavior of complex oxide thin films using electric fields. After providing fundamental definitions of magnetoelectric response, we survey materials, architectures, and mechanisms that exhibit promise for such electric-field control of magnetism. Finally, we mention ideas for future research and discuss prospects for the field.
High-temperature titanium matrix composites reinforced with hybrid reinforcements are synthesized by common casting and hot working technologies. Tensile properties are tested at different temperatures and strain rates. Ultimate strengths of the composites are significantly enhanced under all conditions and decrease when the strain rate is lower. Equicohesive temperature of the matrix is around 873 K at the strain rate 10−3s−1 and well below 873 K at 10−5s−1. At higher temperature or lower strain rate, interfacial debonding is more drastic and reduces the strengths of composites. The materials are embrittled under creep-rupture conditions. Strict reinforcement morphology is required for more complex service conditions at high temperatures in metal matrix composites.