Traditional Ceramics; includes silicates used for clay products such as pottery and bricks, common abrasives and bricks
New Ceramics; more recently developed ceramics based on non-silicates such as oxides and carbides, and generally possessing mechanical and physical properties that are superior or unique compared to traditional ceramics
Glasses: primarily based on silica and distinguished from the other ceramics by their noncrystalline structure. Glass ceramics are glasses that have been transformed into a largely crystalline structure by heat treatment.
Ceramics have covalent and ionic bonding. These bonds are stronger than metallic bonding in metals, which accounts for high hardness, stiffness and low ductility of ceramics
High bonding of electrons makes ceramics poor conductors as opposed to free electrons in metals which makes metals good thermal and electrical conductors
The strong bonding also provides ceramics with high melting point
Some ceramics decompose instead of melting
Most ceramics have crystalline structures, which are more complex than those of metals. The structures of ceramics are more complex than those of metals because Ceramic molecules consist of atoms that are significantly different in size, Ion charges are different, Most ceramic materials consist of more than two elements leading to further complexity in the molecular structures
Mechanical and physical properties are affected by Grain size (high strength + toughness are in fine grained materials)
Some ceramics assume an amorphous structure or glassy phase rather than a crystalline form, e.g. glass
Hardness and elastic modulus for many of the new ceramics are better/greater than for metals
Stiffness and hardness of traditional ceramics and glasses are significantly less than for new ceramics
Theoretically, ceramics should have high strength than metals because of the covalent and ionic bonds (stronger than metallic bonding) But metallic bonding is better in that it allows slip mechanisms by which metals deform plastically. Bonding in ceramics is so rigid that it does not allow slip. Inability of ceramics to slip reduces ability to withstand stress. Yet ceramics contain similar imperfections like metals, i.e. vacancies, interstitialcies, displaced atoms, and microscopic cracks. These internal flaws concentrate stress. The random nature of the imperfections and the influence of the processing variables especially for traditional ceramics make their performance much less predictable.
2. Decreasing grain size in polycrystalline ceramic products
3. Minimizing porosity
4. Introducing compressive surface stresses; for example, through application of glazes with low thermal expansions, so that the body of the product contracts after firing more than the glaze, thus putting the glaze in compression
5. Using fibre reinforcement
6. Heat treatments such as quenching alumina from temperatures in the slightly plastic region to strengthen it.
Most inorganic glasses can be made to transform from a non crystalline state to one that is crystalline by the proper high-temperature heat treatment. This process is called devitrification, and the product is a fine-grained polycrystalline material which is often called a glass–ceramic.
When mixed in the proper proportions, clay and water form a plastic mass that is very amenable to shaping. The formed piece is dried to remove some of the moisture, after which it is fired at an elevated temperature to improve its mechanical strength.
Become white after the high-temperature firing. Included in this group are porcelain, pottery, tableware, and plumbing fixtures (sanitary ware). In addition to clay, many of these products also contain other ingredients, each of which has some role to play in the processing and characteristics of the finished piece.
The capacity to withstand high temperatures without melting or decomposing, and the capacity to remain unreactive and inert when exposed to severe environments
The ability to provide thermal insulation is often an important consideration
Raw ingredients consisting of both large (or grog) particles and fine particles, which may have different compositions
Upon firing, the fine particles normally are involved in the formation of a bonding phase, which is responsible for the increased strength of the brick; this phase may be predominantly either glassy or crystalline
The service temperature is normally below that at which the refractory piece was fired
Porosity is one microstructural variable that must be controlled to produce a suitable refractory brick. Strength, load-bearing capacity, and resistance to attack by corrosive materials all increase with porosity reduction. At the same time, thermal insulation characteristics and resistance to thermal shock are diminished. The choice of the optimum porosity depends on the conditions of service.
The abrasive particles are bonded to a wheel by means of a glassy ceramic or an organic resin. The surface structure should contain some porosity; a continual flow of air currents or liquid coolants within the pores that surround the refractory grains will prevent excessive heating.
An abrasive powder is coated on some type of paper or cloth material e.g. sandpaper. Wood, metals, ceramics, and plastics are all frequently ground and polished using this form of abrasive.
Grinding, lapping, and polishing wheels often employ loose abrasive grains that are delivered in some type of oil- or water-based vehicle. Diamonds, corundum, silicon carbide, and rouge (an iron oxide) are used in loose form over a variety of grain size ranges.
Several familiar ceramic materials are classified as inorganic cements e.g cement, plaster of paris, and lime. The characteristic feature of these materials is that when mixed with water, they form a paste that subsequently sets and hardens.
Solid and rigid structures having just about any shape may be expeditiously formed. Also, some of these materials act as a bonding phase that chemically binds particulate aggregates into a single cohesive structure. Under these circumstances, the role of the cement is similar to that of the glassy bonding phase that forms when clay products and some refractory bricks are fired. One important difference, however, is that the cementitious bond develops at room temperature.
Produced by grinding and intimately mixing clay and lime-bearing minerals in the proper proportions, and then heating the mixture to about 1400°C in a rotary kiln; this process, called calcination, produces physical and chemical changes in the raw materials. The resulting ''clinker'' product is then ground into a very fine powder to which is added a small amount of gypsum (CaSO4·2H2O) to retard the setting process.
Setting time and final strength depend on its composition
The setting and hardening of this material result from hydration reactions that occur between the various cement constituents and the water that is added. The hydrated products are in the form of complex gels or crystalline substances that form the cementitious bond.
Hydration reactions begin just as soon as water is added to the cement. These are first manifested as setting (i.e., the stiffening of the once-plastic paste), which takes place soon after mixing, usually within several hours. Hardening of the mass follows as a result of further hydration, a relatively slow process that may continue for as long as several years.
The process by which cement hardens is not one of drying, but rather, of hydration in which water actually participates in a chemical bonding reaction.