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Science and technology of creating objects from inorganic, non-metallic materials From Wikipedia, the free encyclopedia
Ceramic engineering is the science and technology of creating objects from inorganic, non-metallic materials. This is done either by the action of heat, or at lower temperatures using precipitation reactions from high-purity chemical solutions. The term includes the purification of raw materials, the study and production of the chemical compounds concerned, their formation into components and the study of their structure, composition and properties.
Ceramic materials may have a crystalline or partly crystalline structure, with long-range order on atomic scale. Glass-ceramics may have an amorphous or glassy structure, with limited or short-range atomic order. They are either formed from a molten mass that solidifies on cooling, formed and matured by the action of heat, or chemically synthesized at low temperatures using, for example, hydrothermal or sol-gel synthesis.
The special character of ceramic materials gives rise to many applications in materials engineering, electrical engineering, chemical engineering and mechanical engineering. As ceramics are heat resistant, they can be used for many tasks for which materials like metal and polymers are unsuitable. Ceramic materials are used in a wide range of industries, including mining, aerospace, medicine, refinery, food and chemical industries, packaging science, electronics, industrial and transmission electricity, and guided lightwave transmission.[1]
The word "ceramic" is derived from the Greek word κεραμικός (keramikos) meaning pottery. It is related to the older Indo-European language root "to burn".[2] "Ceramic" may be used as a noun in the singular to refer to a ceramic material or the product of ceramic manufacture, or as an adjective. Ceramics is the making of things out of ceramic materials. Ceramic engineering, like many sciences, evolved from a different discipline by today's standards. Materials science engineering is grouped with ceramics engineering to this day.[citation needed]
Abraham Darby first used coke in 1709 in Shropshire, England, to improve the yield of a smelting process.[citation needed] Coke is now widely used to produce carbide ceramics. Potter Josiah Wedgwood opened the first modern ceramics factory in Stoke-on-Trent, England, in 1759. Austrian chemist Carl Josef Bayer, working for the textile industry in Russia, developed a process to separate alumina from bauxite ore in 1888. The Bayer process is still used to purify alumina for the ceramic and aluminium industries.[citation needed] Brothers Pierre and Jacques Curie discovered piezoelectricity in Rochelle salt c. 1880. Piezoelectricity is one of the key properties of electroceramics.
E.G. Acheson heated a mixture of coke and clay in 1893, and invented carborundum, or synthetic silicon carbide. Henri Moissan also synthesized SiC and tungsten carbide in his electric arc furnace in Paris about the same time as Acheson. Karl Schröter used liquid-phase sintering to bond or "cement" Moissan's tungsten carbide particles with cobalt in 1923 in Germany. Cemented (metal-bonded) carbide edges greatly increase the durability of hardened steel cutting tools. W.H. Nernst developed cubic-stabilized zirconia in the 1920s in Berlin. This material is used as an oxygen sensor in exhaust systems. The main limitation on the use of ceramics in engineering is brittleness.[1]
The military requirements of World War II encouraged developments, which created a need for high-performance materials and helped speed the development of ceramic science and engineering. Throughout the 1960s and 1970s, new types of ceramics were developed in response to advances in atomic energy, electronics, communications, and space travel. The discovery of ceramic superconductors in 1986 has spurred intense research to develop superconducting ceramic parts for electronic devices, electric motors, and transportation equipment.[citation needed]
There is an increasing need in the military sector for high-strength, robust materials which have the capability to transmit light around the visible (0.4–0.7 micrometers) and mid-infrared (1–5 micrometers) regions of the spectrum. These materials are needed for applications requiring transparent armour. Transparent armour is a material or system of materials designed to be optically transparent, yet protect from fragmentation or ballistic impacts. The primary requirement for a transparent armour system is to not only defeat the designated threat but also provide a multi-hit capability with minimized distortion of surrounding areas. Transparent armour windows must also be compatible with night vision equipment. New materials that are thinner, lightweight, and offer better ballistic performance are being sought.[3]
Such solid-state components have found widespread use for various applications in the electro-optical field including: optical fibres for guided lightwave transmission, optical switches, laser amplifiers and lenses, hosts for solid-state lasers and optical window materials for gas lasers, and infrared (IR) heat seeking devices for missile guidance systems and IR night vision.[4]
Now a multibillion-dollar a year industry, ceramic engineering and research has established itself as an important field of science. Applications continue to expand as researchers develop new kinds of ceramics to serve different purposes.[1][5]
Glass-ceramic materials share many properties with both glasses and ceramics. Glass-ceramics have an amorphous phase and one or more crystalline phases and are produced by a so-called "controlled crystallization", which is typically avoided in glass manufacturing. Glass-ceramics often contain a crystalline phase which constitutes anywhere from 30% [m/m] to 90% [m/m] of its composition by volume, yielding an array of materials with interesting thermomechanical properties.[5]
In the processing of glass-ceramics, molten glass is cooled down gradually before reheating and annealing. In this heat treatment the glass partly crystallizes. In many cases, so-called 'nucleation agents' are added in order to regulate and control the crystallization process. Because there is usually no pressing and sintering, glass-ceramics do not contain the volume fraction of porosity typically present in sintered ceramics.[1]
The term mainly refers to a mix of lithium and aluminosilicates which yields an array of materials with interesting thermomechanical properties. The most commercially important of these have the distinction of being impervious to thermal shock. Thus, glass-ceramics have become extremely useful for countertop cooking. The negative thermal expansion coefficient (TEC) of the crystalline ceramic phase can be balanced with the positive TEC of the glassy phase. At a certain point (~70% crystalline) the glass-ceramic has a net TEC near zero. This type of glass-ceramic exhibits excellent mechanical properties and can sustain repeated and quick temperature changes up to 1000 °C.[1][5]
The traditional ceramic process generally follows this sequence: Milling → Batching → Mixing → Forming → Drying → Firing → Assembly.[11][12] [13][14]
Ceramic forming techniques include throwing, slipcasting, tape casting, freeze-casting, injection molding, dry pressing, isostatic pressing, hot isostatic pressing (HIP), 3D printing and others. Methods for forming ceramic powders into complex shapes are desirable in many areas of technology. Such methods are required for producing advanced, high-temperature structural parts such as heat engine components and turbines. Materials other than ceramics which are used in these processes may include: wood, metal, water, plaster and epoxy—most of which will be eliminated upon firing.[11] A ceramic-filled epoxy, such as Martyte, is sometimes used to protect structural steel under conditions of rocket exhaust impingement.[15]
These forming techniques are well known for providing tools and other components with dimensional stability, surface quality, high (near theoretical) density and microstructural uniformity. The increasing use and diversity of specialty forms of ceramics adds to the diversity of process technologies to be used.[11]
Thus, reinforcing fibers and filaments are mainly made by polymer, sol-gel, or CVD processes, but melt processing also has applicability. The most widely used specialty form is layered structures, with tape casting for electronic substrates and packages being pre-eminent. Photo-lithography is of increasing interest for precise patterning of conductors and other components for such packaging. Tape casting or forming processes are also of increasing interest for other applications, ranging from open structures such as fuel cells to ceramic composites.[11]
The other major layer structure is coating, where thermal spraying is very important, but chemical and physical vapor deposition and chemical (e.g., sol-gel and polymer pyrolysis) methods are all seeing increased use. Besides open structures from formed tape, extruded structures, such as honeycomb catalyst supports, and highly porous structures, including various foams, for example, reticulated foam, are of increasing use.[11]
Densification of consolidated powder bodies continues to be achieved predominantly by (pressureless) sintering. However, the use of pressure sintering by hot pressing is increasing, especially for non-oxides and parts of simple shapes where higher quality (mainly microstructural homogeneity) is needed, and larger size or multiple parts per pressing can be an advantage.[11]
The principles of sintering-based methods are simple ("sinter" has roots in the English "cinder"). The firing is done at a temperature below the melting point of the ceramic. Once a roughly-held-together object called a "green body" is made, it is fired in a kiln, where atomic and molecular diffusion processes give rise to significant changes in the primary microstructural features. This includes the gradual elimination of porosity, which is typically accompanied by a net shrinkage and overall densification of the component. Thus, the pores in the object may close up, resulting in a denser product of significantly greater strength and fracture toughness.
Another major change in the body during the firing or sintering process will be the establishment of the polycrystalline nature of the solid. Significant grain growth tends to occur during sintering, with this growth depending on temperature and duration of the sintering process. The growth of grains will result in some form of grain size distribution, which will have a significant impact on the ultimate physical properties of the material. In particular, abnormal grain growth in which certain grains grow very large in a matrix of finer grains will significantly alter the physical and mechanical properties of the obtained ceramic. In the sintered body, grain sizes are a product of the thermal processing parameters as well as the initial particle size, or possibly the sizes of aggregates or particle clusters which arise during the initial stages of processing.
The ultimate microstructure (and thus the physical properties) of the final product will be limited by and subject to the form of the structural template or precursor which is created in the initial stages of chemical synthesis and physical forming. Hence the importance of chemical powder and polymer processing as it pertains to the synthesis of industrial ceramics, glasses and glass-ceramics.
There are numerous possible refinements of the sintering process. Some of the most common involve pressing the green body to give the densification a head start and reduce the sintering time needed. Sometimes organic binders such as polyvinyl alcohol are added to hold the green body together; these burn out during the firing (at 200–350 °C). Sometimes organic lubricants are added during pressing to increase densification. It is common to combine these, and add binders and lubricants to a powder, then press. (The formulation of these organic chemical additives is an art in itself. This is particularly important in the manufacture of high performance ceramics such as those used by the billions for electronics, in capacitors, inductors, sensors, etc.)
A slurry can be used in place of a powder, and then cast into a desired shape, dried and then sintered. Indeed, traditional pottery is done with this type of method, using a plastic mixture worked with the hands. If a mixture of different materials is used together in a ceramic, the sintering temperature is sometimes above the melting point of one minor component – a liquid phase sintering. This results in shorter sintering times compared to solid state sintering.[16] Such liquid phase sintering involves in faster diffusion processes and may result in abnormal grain growth.
A material's strength is dependent on its microstructure. The engineering processes to which a material is subjected can alter its microstructure. The variety of strengthening mechanisms that alter the strength of a material include the mechanism of grain boundary strengthening. Thus, although yield strength is maximized with decreasing grain size, ultimately, very small grain sizes make the material brittle. Considered in tandem with the fact that the yield strength is the parameter that predicts plastic deformation in the material, one can make informed decisions on how to increase the strength of a material depending on its microstructural properties and the desired end effect.
The relation between yield stress and grain size is described mathematically by the Hall-Petch equation which is
where ky is the strengthening coefficient (a constant unique to each material), σo is a materials constant for the starting stress for dislocation movement (or the resistance of the lattice to dislocation motion), d is the grain diameter, and σy is the yield stress.
Theoretically, a material could be made infinitely strong if the grains are made infinitely small. This is, unfortunately, impossible because the lower limit of grain size is a single unit cell of the material. Even then, if the grains of a material are the size of a single unit cell, then the material is in fact amorphous, not crystalline, since there is no long range order, and dislocations can not be defined in an amorphous material. It has been observed experimentally that the microstructure with the highest yield strength is a grain size of about 10 nanometers, because grains smaller than this undergo another yielding mechanism, grain boundary sliding.[17] Producing engineering materials with this ideal grain size is difficult because of the limitations of initial particle sizes inherent to nanomaterials and nanotechnology.
The Faber-Evans model, developed by Katherine Faber and Anthony G. Evans, was developed to predict the increase in fracture toughness in ceramics due to crack deflection around second-phase particles that are prone to microcracking in a matrix.[18] The model considers particle morphology, aspect ratio, spacing, and volume fraction of the second phase, as well as the reduction in local stress intensity at the crack tip when the crack is deflected or the crack plane bows. Actual crack tortuosity is obtained through imaging techniques, which allows for the direct input of deflection and bowing angles into the model.
The model calculates the average strain energy release rate and compares the resulting increase in fracture toughness to that of a flat crack through the plain matrix. The magnitude of the toughening is determined by the mismatch strain caused by thermal contraction incompatibility and the microfracture resistance of the particle/matrix interface. The toughening becomes noticeable with a narrow size distribution of appropriately sized particles, and researchers typically accept that deflection effects in materials with roughly equiaxial grains may increase the fracture toughness by about twice the grain boundary value.[19]
The model reveals that the increase in toughness is dependent on particle shape and the volume fraction of the second phase, with the most effective morphology being the rod of high aspect ratio, which can account for a fourfold increase in fracture toughness. The toughening arises primarily from the twist of the crack front between particles, as indicated by deflection profiles. Disc-shaped particles and spheres are less effective in toughening. Fracture toughness, regardless of morphology, is determined by the twist of the crack front at its most severe configuration, rather than the initial tilt of the crack front. Only for disc-shaped particles does the initial tilting of the crack front provide significant toughening; however, the twist component still overrides the tilt-derived toughening.[20]
Additional important features of the deflection analysis include the appearance of asymptotic toughening for the three morphologies at volume fractions in excess of 0.2. It is also noted that a significant influence on the toughening by spherical particles is exerted by the interparticle spacing distribution; greater toughening is afforded when spheres are nearly contacting such that twist angles approach π/2. These predictions provide the basis for the design of high-toughness two-phase ceramic materials.
The ideal second phase, in addition to maintaining chemical compatibility, should be present in amounts of 10 to 20 volume percent. Greater amounts may diminish the toughness increase due to overlapping particles. Particles with high aspect ratios, especially those with rod-shaped morphologies, are most suitable for maximum toughening. This model is often used to determine the factors that contribute to the increase in fracture toughness in ceramics which is ultimately useful in the development of advanced ceramic materials with improved performance.[21][22]
In the processing of fine ceramics, the irregular particle sizes and shapes in a typical powder often lead to non-uniform packing morphologies that result in packing density variations in the powder compact. Uncontrolled agglomeration of powders due to attractive van der Waals forces can also give rise to in microstructural inhomogeneities.[11][23]
Differential stresses that develop as a result of non-uniform drying shrinkage are directly related to the rate at which the solvent can be removed, and thus highly dependent upon the distribution of porosity. Such stresses have been associated with a plastic-to-brittle transition in consolidated bodies,[24] and can yield to crack propagation in the unfired body if not relieved.
In addition, any fluctuations in packing density in the compact as it is prepared for the kiln are often amplified during the sintering process, yielding inhomogeneous densification.[25][26] Some pores and other structural defects associated with density variations have been shown to play a detrimental role in the sintering process by growing and thus limiting end-point densities.[27] Differential stresses arising from inhomogeneous densification have also been shown to result in the propagation of internal cracks, thus becoming the strength-controlling flaws.[28]
It would therefore appear desirable to process a material in such a way that it is physically uniform with regard to the distribution of components and porosity, rather than using particle size distributions which will maximize the green density. The containment of a uniformly dispersed assembly of strongly interacting particles in suspension requires total control over particle-particle interactions. Monodisperse colloids provide this potential.[29]
Monodisperse powders of colloidal silica, for example, may therefore be stabilized sufficiently to ensure a high degree of order in the colloidal crystal or polycrystalline colloidal solid which results from aggregation. The degree of order appears to be limited by the time and space allowed for longer-range correlations to be established.[30][31]
Such defective polycrystalline colloidal structures would appear to be the basic elements of sub-micrometer colloidal materials science, and, therefore, provide the first step in developing a more rigorous understanding of the mechanisms involved in microstructural evolution in inorganic systems such as polycrystalline ceramics.
Self-assembly is the most common term in use in the modern scientific community to describe the spontaneous aggregation of particles (atoms, molecules, colloids, micelles, etc.) without the influence of any external forces. Large groups of such particles are known to assemble themselves into thermodynamically stable, structurally well-defined arrays, quite reminiscent of one of the 7 crystal systems found in metallurgy and mineralogy (e.g. face-centered cubic, body-centered cubic, etc.).[citation needed] The fundamental difference in equilibrium structure is in the spatial scale of the unit cell (or lattice parameter) in each particular case.
Thus, self-assembly is emerging as a new strategy in chemical synthesis and nanotechnology. Molecular self-assembly has been observed in various biological systems and underlies the formation of a wide variety of complex biological structures. Molecular crystals, liquid crystals, colloids, micelles, emulsions, phase-separated polymers, thin films and self-assembled monolayers all represent examples of the types of highly ordered structures which are obtained using these techniques. The distinguishing feature of these methods is self-organization in the absence of any external forces.[citation needed]
In addition, the principal mechanical characteristics and structures of biological ceramics, polymer composites, elastomers, and cellular materials are being re-evaluated, with an emphasis on bioinspired materials and structures. Traditional approaches focus on design methods of biological materials using conventional synthetic materials. This includes an emerging class of mechanically superior biomaterials based on microstructural features and designs found in nature. The new horizons have been identified in the synthesis of bioinspired materials through processes that are characteristic of biological systems in nature. This includes the nanoscale self-assembly of the components and the development of hierarchical structures.[30][31][33]
Substantial interest has arisen in recent years in fabricating ceramic composites. While there is considerable interest in composites with one or more non-ceramic constituents, the greatest attention is on composites in which all constituents are ceramic. These typically comprise two ceramic constituents: a continuous matrix, and a dispersed phase of ceramic particles, whiskers, or short (chopped) or continuous ceramic fibers. The challenge, as in wet chemical processing, is to obtain a uniform or homogeneous distribution of the dispersed particle or fiber phase.[34] [35]
Consider first the processing of particulate composites. The particulate phase of greatest interest is tetragonal zirconia because of the toughening that can be achieved from the phase transformation from the metastable tetragonal to the monoclinic crystalline phase, aka transformation toughening. There is also substantial interest in dispersion of hard, non-oxide phases such as SiC, TiB, TiC, boron, carbon and especially oxide matrices like alumina and mullite. There is also interest too incorporating other ceramic particulates, especially those of highly anisotropic thermal expansion. Examples include Al2O3, TiO2, graphite, and boron nitride.[34][35]
In processing particulate composites, the issue is not only homogeneity of the size and spatial distribution of the dispersed and matrix phases, but also control of the matrix grain size. However, there is some built-in self-control due to inhibition of matrix grain growth by the dispersed phase. Particulate composites, though generally offer increased resistance to damage, failure, or both, are still quite sensitive to inhomogeneities of composition as well as other processing defects such as pores. Thus they need good processing to be effective.[1][5]
Particulate composites have been made on a commercial basis by simply mixing powders of the two constituents. Although this approach is inherently limited in the homogeneity that can be achieved, it is the most readily adaptable for existing ceramic production technology. However, other approaches are of interest.[1][5]
From the technological standpoint, a particularly desirable approach to fabricating particulate composites is to coat the matrix or its precursor onto fine particles of the dispersed phase with good control of the starting dispersed particle size and the resultant matrix coating thickness. One should in principle be able to achieve the ultimate in homogeneity of distribution and thereby optimize composite performance. This can also have other ramifications, such as allowing more useful composite performance to be achieved in a body having porosity, which might be desired for other factors, such as limiting thermal conductivity.
There are also some opportunities to utilize melt processing for fabrication of ceramic, particulate, whisker and short-fiber, and continuous-fiber composites. Clearly, both particulate and whisker composites are conceivable by solid-state precipitation after solidification of the melt. This can also be obtained in some cases by sintering, as for precipitation-toughened, partially stabilized zirconia. Similarly, it is known that one can directionally solidify ceramic eutectic mixtures and hence obtain uniaxially aligned fiber composites. Such composite processing has typically been limited to very simple shapes and thus suffers from serious economic problems due to high machining costs.[34][35]
Clearly, there are possibilities of using melt casting for many of these approaches. Potentially even more desirable is using melt-derived particles. In this method, quenching is done in a solid solution or in a fine eutectic structure, in which the particles are then processed by more typical ceramic powder processing methods into a useful body. There have also been preliminary attempts to use melt spraying as a means of forming composites by introducing the dispersed particulate, whisker, or fiber phase in conjunction with the melt spraying process.
Other methods besides melt infiltration to manufacture ceramic composites with long fiber reinforcement are chemical vapor infiltration and the infiltration of fiber preforms with organic precursor, which after pyrolysis yield an amorphous ceramic matrix, initially with a low density. With repeated cycles of infiltration and pyrolysis one of those types of ceramic matrix composites is produced. Chemical vapor infiltration is used to manufacture carbon/carbon and silicon carbide reinforced with carbon or silicon carbide fibers.
Besides many process improvements, the first of two major needs for fiber composites is lower fiber costs. The second major need is fiber compositions or coatings, or composite processing, to reduce degradation that results from high-temperature composite exposure under oxidizing conditions.[34][35]
The products of technical ceramics include tiles used in the Space Shuttle program, gas burner nozzles, ballistic protection, nuclear fuel uranium oxide pellets, bio-medical implants, jet engine turbine blades, and missile nose cones.
Its products are often made from materials other than clay, chosen for their particular physical properties. These may be classified as follows:
Ceramics can be used in many technological industries. One application is the ceramic tiles on NASA's Space Shuttle, used to protect it and the future supersonic space planes from the searing heat of re-entry into the Earth's atmosphere. They are also used widely in electronics and optics. In addition to the applications listed here, ceramics are also used as a coating in various engineering cases. An example would be a ceramic bearing coating over a titanium frame used for an aircraft. Recently the field has come to include the studies of single crystals or glass fibers, in addition to traditional polycrystalline materials, and the applications of these have been overlapping and changing rapidly.
Silicification is quite common in the biological world and occurs in bacteria, single-celled organisms, plants, and animals (invertebrates and vertebrates). Crystalline minerals formed in such environment often show exceptional physical properties (e.g. strength, hardness, fracture toughness) and tend to form hierarchical structures that exhibit microstructural order over a range of length or spatial scales. The minerals are crystallized from an environment that is undersaturated with respect to silicon, and under conditions of neutral pH and low temperature (0–40 °C). Formation of the mineral may occur either within or outside of the cell wall of an organism, and specific biochemical reactions for mineral deposition exist that include lipids, proteins and carbohydrates.
Most natural (or biological) materials are complex composites whose mechanical properties are often outstanding, considering the weak constituents from which they are assembled. These complex structures, which have risen from hundreds of million years of evolution, are inspiring the design of novel materials with exceptional physical properties for high performance in adverse conditions. Their defining characteristics such as hierarchy, multifunctionality, and the capacity for self-healing, are currently being investigated.[39]
The basic building blocks begin with the 20 amino acids and proceed to polypeptides, polysaccharides, and polypeptides–saccharides. These, in turn, compose the basic proteins, which are the primary constituents of the 'soft tissues' common to most biominerals. With well over 1000 proteins possible, current research emphasizes the use of collagen, chitin, keratin, and elastin. The 'hard' phases are often strengthened by crystalline minerals, which nucleate and grow in a bio-mediated environment that determines the size, shape and distribution of individual crystals. The most important mineral phases have been identified as hydroxyapatite, silica, and aragonite. Using the classification of Wegst and Ashby, the principal mechanical characteristics and structures of biological ceramics, polymer composites, elastomers, and cellular materials have been presented. Selected systems in each class are being investigated with emphasis on the relationship between their microstructure over a range of length scales and their mechanical response.
Thus, the crystallization of inorganic materials in nature generally occurs at ambient temperature and pressure. Yet the vital organisms through which these minerals form are capable of consistently producing extremely precise and complex structures. Understanding the processes in which living organisms control the growth of crystalline minerals such as silica could lead to significant advances in the field of materials science, and open the door to novel synthesis techniques for nanoscale composite materials, or nanocomposites.
High-resolution scanning electron microscope (SEM) observations were performed of the microstructure of the mother-of-pearl (or nacre) portion of the abalone shell. Those shells exhibit the highest mechanical strength and fracture toughness of any non-metallic substance known. The nacre from the shell of the abalone has become one of the more intensively studied biological structures in materials science. Clearly visible in these images are the neatly stacked (or ordered) mineral tiles separated by thin organic sheets along with a macrostructure of larger periodic growth bands which collectively form what scientists are currently referring to as a hierarchical composite structure. (The term hierarchy simply implies that there are a range of structural features which exist over a wide range of length scales).[40]
Future developments reside in the synthesis of bio-inspired materials through processing methods and strategies that are characteristic of biological systems. These involve nanoscale self-assembly of the components and the development of hierarchical structures.[30][31][33][41]
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