Digitalfire Ceramic Glossary

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  • Majolica

    Pottery fired to a low temperature employing a red-burning terra cotta clay covered with a soft opaque white glaze. Historically, majolica glazes (or tin glazed earthenware) were opacified using Tin Oxide, but now Zirconium silicate is most often used. Most majolica also has colored brushwork designs that are painted over the dried glaze (the painting process is tricky because you are painting on a very absorbent surface, you get one brush stroke!). Metallic colorants are brightest at low temperatures and the zircon-stiffened white glaze provides an ideal canvas for them. Colorant formulations (mixtures of stain powders, melters, hardeners, fillers) need to be tuned to melt enough so that they become one with the glaze below, but not so much that they bleed excessively at the edge of brush strokes. Different families of stains have different melting behaviors and chemistry requirements for the host glaze and medium (the color development and degree of melting in the final firing product depend on this). You can buy premixed majolica colors and often these work well, but do not assume that just because it comes in a jar it is perfect or that you cannot formulate something better for your application.

    Ware made using the Majolica process is not strong, the clays generally have 10% porosity or more (fired at cone 06-04). This low temperature means that the body-glaze interface is much less developed than in stoneware (so the glaze is not stuck on nearly as well). It is thus important that the thermal expansion of the glaze be matched to the body to prevent crazing and shivering. Ware is not as durable in use and any bare sections will absorb water and tend to water-log the clay matrix over time. It is thus best to make a foot ring so that the entire piece can be glazed, leaving only a narrow channel of exposed body to touch the kiln shelf.

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    • (Glossary) Earthenware

      A clay fired at low temperatures (cone 010-02) whe...


    Pictures

    Example of a terra cotta clay fired at cone 04 and cone 02. Courtesy of Plainsman Clays.

    Fired test bars of different terra cotta clays fired at different temperatures. You can see varying levels of maturity (or vitrification), DFAC disk showing solubles on an iron stoneware

    A dried terra cotta mug on the left, bisque fired to cone 06 on the right.

    I have made bi-body strips for testing to tune a slip for a terra cotta clay body (about 4 mm thick). They need to shrink a similar amount in drying and firing to be as compatible as possible. Here, the white body needs more plastic clay or a bentonite addition to shrink more. It also needs a little less frit or a coarser silica to shrink a little less on firing (pending porosity tests to match their fired density). Amazingly, the fired bars break much more easily one way that the other, because on one side the clay is being stretched (and ceramic does not do well under tension).

    This is part of a project to fit a slip onto terracotta for cone 02. Left: On drying red body A curls the bi-clay strip toward itself (back), but on firing it goes the other way (front)! Front: Red body B dries and fires straight with the white slip (which is actually just a white body with added frit to make it mature at cone 02). Right: I made test bars of the white body and red body B so I can measure (and compare) the drying shrinkage and porosity at cones 04,03,02,01,1. Center back: A cone 02 fired mug with the white slip and a transparent overglaze. We have a problem: the slip is going translucent under the glaze. That means I have two options: The slip needs zircon added or I will have to reduce the frit content and tolerate a less vitreous and therefore less durable and attached slip.

  • Marbling

    The practice of mixing porcelains of two or more different colors (the porcelains are typically colored using metal oxides or stains). To produce a quality fired product it is important that the clays are the same stiffness and have the same drying and fired shrinkages and the same thermal expansions.
    Pictures

    A transparent glazed marbled bowl by Tony Hansen. It is a made from a New Zealand kaolin based porcelain fired at cone 6. The blue is from Mason 6306 teal blue stain.

  • Material Expansion

    Ceramic materials exhibit thermal expansions just as fired bodies. Manufactured materials, like frits, have a consistent easily measured thermal expansion because they are completely melted during processing. They also calculate well, that is, the thermal expansion can be predicted. Raw materials, on the other hand are complex (expecially clays). Many raw materials are not homogeneous, thus when subjected to the heat of a kiln, different particles within the powder matrix will exhibit different thermal expansion characteristics (some of which can be multi-stage) and they interact in complex ways. For example, some may be refractory and resist melting, others may form a glass melt and take yet others into solution while still others may interact to create new crystalline species that survive for a period and then inturn interact for a time and finally go into solution or melt. If a material was fired alone the final thermal expansion would be a product of the extent to which all of this was allowed to proceed (according to the temperature the kiln reached). Thus, while it may be practical to publish the thermal expansion of a frit for calculation purposes, this is not practical with the vast majority of raw materials. It is better to calculate the expansion of the glaze into which they are incorporated based on the calculated quantities of each oxide. Of course, the reliability of the calculation is also based on whether the glaze completes melts or not.

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    • (Troubles) Glaze Crazing
      Ask the right questions to analyse the real cause ...
  • Material Substitution

    Material substitution is a constant and ongoing part of any ceramic enterprise that is using clay and/or glaze recipes. Often lack of availability, quality issues and price are the motivating factors. In addition, when recipes need to be used in another locality where the same raw material brands or even types are unavailable, substitutions must be done.

    In ceramics, glazes fire the way they do primarily because of their chemistry. The most basic substitution is to simply replace one material for another which has a chemistry similar enough that the fired properties will not be adversely affected. This is often possible with different brand names of the same mineral or refined material (e.g. Calcium carbonate, zinc oxide). The more complex the chemistry of the raw material, the more likely there is to be issues with changes to another (e.g. feldspar). In some cases substitution recipes are recommended where a mix of two or more other materials is said to be equivalent. Another problem can occur where, although the chemistry of the substitute is very similar, it's physical properties or particle size are different enough to affect the working properties of the glaze (e.g. a kaolin) or even it's fired appearance (a metal oxide).

    A given chemistry can be supplied by many different mixes of refined and raw material powders, each of these having advantages and disadvantages regarding price, ease of use in production, toxicity, etc. It is common to use ceramic chemistry to calculate how to juggle a recipe to substitute one material for another of slightly or even very different chemistry while maintaining the chemistry of the glaze as a whole. The calculcation is more complex where the substitute is bringing along other oxides not in the material being substituted (or fewer) or the original or substitute has a very different weight loss on firing (LOI). Frits especially can have complex chemistries and obviously it is more complciated if they are involved in the substitution calculation.

    When clay bodies and porcelains require material substitution, the issue is physical properties (which are often not directly related to chemistry). Thus testing must be done to see how maturity, drying properties, plastic and/or forming behavior, texture, firing color and character, thermal expansion and other properties are affected. A series of tests usually must be done to alter the recipe to accommodate the new material while maintaining the needed properties.

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  • Matte Glaze

    A glaze that is not glossy. Of course, unmelted glazes will not be glossy, but to be a true matte a glaze must be melted and still not glossy. To be a functional matte it must also resist cultery marking, clean well and not leach into food and drink. Thus it is not easy to make a good matte glaze. It is common to see poor quality matte surfaces on name-brand table ware sold in major stores.

    The vast majority of random material mixes that melt well want to be glossy. Matteness can be a product of the physical or mineral form of a material used, the chemistry and selection of materials to source that chemistry and often the firing schedule. While some types of mattes are stable, with others it can be difficult to maintain the same fired texture through material and firing variations. The best mattes are those whose mechanism is understood and have an adjuster (a firing change or a material whose percentage can be raised or lowered to fine tune the degree or character of the matteness).

    The visual character of mattes, even those within the same mechanism, varies widely and is often difficult to characterize. Matteness is often part of a larger visual character that involves color and variegation.

    Mechanisms that produce matte glazes produce surfaces that scatter light:
    -Micro crystalline surfaces. High CaO glazes, for example, form minute calcium silicate crystals when cooling (at normal cooling rates). Wollastonite especially can do this, but also other sources of CaO. Another oxide that crystallizes well if oversupplied is ZnO, the size of the crystal being determined by the rate of cooling and level of ZnO.
    -Micro-wavy or rippled (non flat) surfaces can be produced multiple ways. High Al2O3 (if supplied in a form that can decompose to enable Al2O3 to enter the melt), for example, stiffens the melt preventing level-out during cooling. Glaze melts that contain multiple melt phases solidify in a non-homogeneous way to produce a glass that both scatters light from within and from its surface.
    -A special case of micro-rippled surfaces is MgO. It is a very effective matting agent at both high and middle temperatures. Talc and dolomite source the MgO to create this effect (although can differ in appearance). In higher temperatures the MgO creates multiple phases in the melt that have different fluidity and refractive indexes. These are sometimes called 'silky mattes' and are pleasant to the touch. Amazingly MgO also produces this effect at middle temperatures even though it is not an active melter there. Levels of 0.3 or higher will stiffen the melt without detrimentally affecting glass development and produce very pleasant matte surfaces. This works in boron fluxed glazes that have high or low Al2O3 and low or medium SiO2 levels, producing surfaces that do not cutlery mark and glazes that do not craze (because of the low expansion of MgO).
    -Crowbar method! Materials whose individual particles are so refractory that they simply do not dissolve in the melt, if added judiciously to the right base, can produce a workable matte. Magnesium carbonate is an example. Even calcium carbonate, if supplied in raw form, does not melt at lower temperatures and can thus matte a glaze. But the best example is calcined alumina, if used in sufficiently fine particle size, can matte a glaze even with a small addition. However, alumina hydrate, by contrast requires a much greater addition. Why? It enters the chemistry of the melt and imparts a true alumina matte, the latter just increases the melting temperature because it is so refractory.
    -Mechanisms that are not well understood. An example is barium mattes. Although they appear to be crystallized, some have found that no matter how fast they are cooled they still have the same degree of matteness. At the same time, fritted forms of the same amount of barium do not matte! In this system it appears the carbonate form supplies the BaO and seeds the crystals.

    Employing combinations of these mechanisms is normally not practical because they can conflict. For example, a crystal matte is based on a highly fluid, well melting glaze, whereas an alumina matte is the opposite. However an exception to this is magnesia mattes, they can occur where alumina is high and silica is low (the alumina matte mechanism, although MgO can matte glazes that also have low MgO).

    Functional matte glazes are more difficult to formulate (especially at middle and low temperatures) because they have a narrow window of chemistries or have recipes containing matting agents that are highly active (resulting in large changes in the degree matteness for small variations in the recipe or process). For crystal mattes, specific firing methods are also needed (e.g. slower cooling). Also, the degree to which mattes do not level out completely on cooling determines how easy-to-clean the surface of the glass will be.

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    Pictures

    The reflection of light on a matte glaze

    GR10-J Ravenscrag silky matte (right) and G2571A matte (left) on a buff stoneware at cone 10R. Surfaces feel identical, the slightly darker color is due to iron content in the Ravenscrag.

    Cone 6 melt flow comparison between a poorly fluxed matte (having no boron, zinc or lithia) and well fluxed glossy glaze.

    A cone 5 flow test between the glossy G1214W (left) and matte G1214Z. True mattes are fluid and should melt as well as glossies, this matte is actually melting more!

    2,5,10,15% talc added to Ravenscrag Slip on a buff stoneware fired at cone 10R. Matting begins at 10%. By Kat Valenzuela.

    2,5,10,15% calcined alumina added to Ravenscrag Slip on a buff stoneware fired at cone 10R. Matting begins at 5% producing a very dry surface by 15%. Alumina hydrate works better. By Kat Valenzuela.

    2,5,10,15% dolomite added to Ravenscrag Slip on a buff stoneware fired at cone 10R. Crystal development toward a dolomite matte begins at 15%. By Kat Valenzuela.

    2,5,10,15% alumina hydrate added to Ravenscrag Slip on a buff stoneware fired at cone 10R. Crazing starts at cone 10% creating an alumina matte by 15%. By Kat Valenzuela.

    Make cone 10R bamboo colors with GR10-J Ravenscrag silky matte base (right) by adding 1% iron (left), (0.5% centre). These samples are porcelain. This also works with G2571A matte.

    These are two cone 6 matte glazes (shown side by side in an account at Insight-live). G1214Z is high calcium and a high silica:alumina ratio (you can find more about it by googling 1214Z). It crystallizes during cooling to make the matte effect and the degree of matteness is adjustable by trimming the silica content (but notice how much it runs). The G2928C has high MgO and it produces the classic silky matte by micro-wrinkling the surface, its matteness is adjustable by trimming the calcined kaolin. CaO is a standard oxide that is in almost all glazes, 0.4 is not high for it. But you would never normally see more than 0.3 of MgO in a cone 6 glaze (if you do it will likely be unstable). The G2928C also has 5% tin, if that was not there it would be darker than the other one because Ravenscrag Slip has a little iron. This was made by recalculating the Moore's Matte recipe to use as much Ravenscrag Slip as possible yet keep the overall chemistry the same. This glaze actually has texture like a dolomite matte at cone 10R, it is great. And it has wonderful application properties. And it does not craze, on Plainsman M370 (it even survived and 300F to ice water plunge without cracking). This looks like it could be a great liner glaze.

    Two cone 6 matte glaze mechanisms. G2934 is an MgO saturated boron fluxed glaze that melts to the right degree, forms a good glass, has a low thermal expansion, resists leaching and does not cutlery mark. G2000 is LA Matte, a much trafficked cone 6 recipe, it is fluxed by zinc to produce a surface mesh of micro-crystals that not only mattes but also opacifies the glaze. But it forms a poor glass, runs too much, cutlery marks badly, stains easily and crazes!

    Matte glazes have a fragile mechanism. That means the same recipe will be more matte for some people, more glossy for others (due to material, process and firing differences). In addition, certain colors will matte the base more and others will gloss it more. It is therefore critical for matte glaze recipes to have adjustability (a way to change the degree of gloss), both for circumstances and colors. This recipe is Plainsman G2934 base matte with 6% Mason 6600 black stain added. It has been formulated to be on the more matte side of the scale so that for most people a simple addition of G2926B (M370 transparent ultra clear base recipe) will increase the gloss. That means users need to be prepared to adjust each color of the matte to fine tune its degree of gloss. Here you can see 5, 10, 15 and 20% additions of the gloss recipe.

    GR10-J Ravenscrag dolomite matte base glaze at cone 10R on Plainsman H443 iron speckled clay. This recipe was created by starting with the popular G2571 base recipe (googleable) and calculating a mix of materials having the maximum possible Ravenscrag Slip percentage. The resultant glaze has the same excellent surface properties (resistance to staining and cutlery marking) but has even better application and working properties. It is a little more tan in color because of the iron content of Ravenscrag Slip (see ravenscrag.com).

  • Mature

    A term referring to the degree to which a clay or glaze has vitrified or melted in the kiln. A 'mature' stoneware or porcelain clay is normally one that is dense and strong, a 'mature' glaze flows well and heals imperfections to provide a good covering. Like the term 'vitrification' mature needs to be taken in context. A mature sintered refractory, for example is quite porous and would be considered immature for other uses.

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    • (Glossary) Functional

      A functional clay body is one that produces a cera...


    Pictures

    Fired test bars of different terra cotta clays fired at different temperatures. You can see varying levels of maturity (or vitrification), DFAC disk showing solubles on an iron stoneware

  • MDT

    Materials Definition Table. The materials database of Digitalfire Insight ceramic chemistry software. It is called a table because Insight reads it into memory at program startup and forms and internal data structure of material rows and oxide columns that it references to do calculations of recipes containing the materials.

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  • Medium Temperature or Mid-Fire Glaze

    In functional ceramics this term generally refers to glazes that mature from cone 4 to 7. At these temperatures it is difficult to compound glazes that will melt well without the need for powerful melters like zinc and boron. Thus a medium temperature glaze contains mostly the same kinds of ingredients as a high temperature one, but additionally it needs a source of zinc or boron (boron is by far more popular and less troublesome). Typically frits are employed to supply the B2O3. Historically Gerstley Borate and Colemanite were very common sources also. Boron has a low thermal expansion and thus is an ideal additive since it reduces the tendency of glazes to craze. Since there are no practical insoluble sources of pure boron, ceramic chemistry is normally needed to determine how to best incorporate boron-sourcing materials.

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  • Melting Temperature

    Unlike crystalline minerals, glazes do not really have a melting temperature, they generally soften over a range. The reason they soften can be two fold. First, raw glazes contain particles of many types, each having its own melting behavior. Fluxes melt first, perhaps suddenly, then they dissolve other particles slowly until the entire mass is melted. Most fritted glazes normally melt more slowly simply because frits are pre-melted, quenched in water and ground (by definition, glasses soften or melt slowly).

    The complexities of oxide interactions and firing methods along with the wide range of physical and mineralogical properties of materials supplying oxides make the prediction of absolute values for fired properties an inexact and highly system-specific science at best. This is especially the case with melting temperature prediction.

    However ceramic calculations work well as a relative science. INSIGHT's dual recipe functionality makes it a natural for studying one recipe in relation to another with respect to maturing temperature, expansion, etc. Technicians change the chemistry of a recipe according to a knowledge of what direction the change should take the desired property. Then they relate fired results back to the chemical change and build understanding to use for subsequent fine tuning. It is common to develop prediction skills within specific 'oxide systems'. We teach people the interpretation skills they need to do this. Digitalfire is very hesitant to build temperature prediction into INSIGHT for fear it would make us appear in any way naive about this.

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    Pictures

    Example of how a frit softens over a wide temperature range

    Feldspar and talc are both flux sources (glaze melters). But the fluxes (Na2O and MgO) within these materials need the right mix of other oxides with which to interact to vitrify or melt a mix. The feldspar does source other oxides for the Na2O to interact with, but lacks other fluxes and the proportions are not right, it is only beginning to soften at cone 6. The soda frit is already very active at cone 06! As high as cone 6, talc (the best source of MgO) shows no signs of melting activity at all. But a high MgO frit is melting beautifully at cone 06. While the frits are melting primarily because of the boron content, the Na2O and MgO have become active participants in the melting of a low temperature glass. In addition, the oxides exist in a glass matrix that is much easier to melt than the crystal matrix of the raw materials.

  • Metallic or Bronze Glazes

    Glassy iridescent metallic glazes can most easily be produced in oxidation using very high a percentage of manganese dioxide (the metal fumes of which can be very dangerous) in a borax or lead based frit or glaze. Manganese is an active melter, so 50% or it and a borax frit will produce a very fluid glaze at cone 6. Other metal oxides like copper and cobalt are also active fluxes and melt even better than manganese, but they want to form crystals during cooling (the micro-crystals of copper completely matte the surface). To utilize copper and cobalt a frit base of high alumina is required to make the melt stiff enough to resist crystal formation.

    Up to 80% metal oxide is sometimes used. If crystals are desired, their development can be encouraged by adding a catalyst (e.g. barium carbonate). As noted, these glazes can be very toxic to fire because of the danger of the metallic fumes. They are completely unsuitable for use on functional surfaces.

    In reduction firing it is obviously easier to produce metallic surfaces, thus much lower amounts are needed. A key reason for this is that iron, while refractory in oxidation, is an active flux in reduction. In addition, iron oxide is inexpensive whereas the other metal oxides useful for this purpose are very, very expensive. Bronze-like surfaces can also be made by the addition of rutile.

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    Pictures

    Metallic oxides with 50% Ferro frit 3134 in crucibles at cone 6ox. Chrome and rutile have not melted, copper and cobalt are extremely active melters. Cobalt and copper have crystallized during cooling, manganese has formed an iridescent glass.

    This is a metallic silky crystal black, it is Alberta Slip plus 5% Mason 6600 black stain, 5% Mason 6666 black and 7% iron.

    Metallic deep purple by firing pure alberta slip at cone 10R, then refiring at cone 6 oxidation.

  • Microwave Safe

    This is a term relating to the ability of a ceramic to resist fracture and super-heating during exposure to the micro waves. Porous bodies that can absorb water into the matrix which cannot quickly escape as steam are an obvious danger, especially where the ceramic is glazed (crazed glazes, unglazed footrings can provide channels for gradual water logging of a piece). Another obvious factor is the avoidance of body materials containing particles of iron (or high iron minerals) or red burning bodies simply having a high iron content. Of course, the same goes for other metallics. Glazes of high iron oxide powder content (or other metal oxide) could also be an issue. In addition, ware should be of even cross section and not overly thick. Simple common sense and testing will suffice to prove the suitability of a ceramic. To test, just put a little water in a piece and try it in a microwave for 30 seconds, if it feels a lot hotter than the water then there is a problem.

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    • (Articles)

      Is Your Fired Ware Safe?

      Glazed ware can be a safety hazard to end users because it may leach metals into food and drink, it ...

  • Mineral

    Ceramic minerals have a highly ordered atomic structure and a specific range of crystalline manifestations. A given chemistry can exhibit itself in more than one mineral form, each having its own crystalline structure and physical properties. Minerals can have phases or different crystalline forms and these can be converted one to another by the application of specific heating and cooling curves and exist between specific temperatures (thus certain mineral may only exist during a firing, you will never be able to hold them in your hand). The most common mineral is quartz, it can exist in a variety of forms (e.g. tridymite, cristobalite). Mica and mullite are good examples of materials used in ceramics exclusively for their mineralogy, not their chemistry. Many ceramic minerals are silicates. Minerals have specific melting temperatures and well defined events in their thermal decomposition history. Materials are mixtures of minerals and material powders are mixtures of microscopic mineral particles.

    Understanding that quartz mineral and silica glass have vastly different physical properties is often the beginnings of understanding the relationship between the mineralogy of the materials we use and their chemistry. Fused silica, for example, is one of the lowest thermal expansion materials available (0.2% at 2000F). Some industries, for example, use fused silica slabs weighing more than a ton as valves in large pipes where temperatures are not only high but suddenly change, yet these slabs do not crack. These slabs operate continuously at high temperatures, however at plant shut down when they are cooled they crystallize and must be discarded! Quartz, on the other hand, is one of the least thermal-expansion-tolerant minerals (1.5% at 2000F) and even thin sections crack very easily on sudden temperature changes. Yet both have the same SiO2 chemistry.

    Understanding minerals also involves understanding how CO2 and H2O incorporate into the crystal structure of so many minerals and how to adapt a firing process withstand expulsion or how to process the mineral to take these out and store it to keep them out.

    A good example of where a potter needs to consider mineralogy is when he is formulating a clay based engobe to apply over earthenware or low fire stoneware. The amount of quartz mineral in the body and slip needs to match fairly closely to minimize chances of the slip-body bond being compromised as the piece is cooled through quartz inversion.

    More technical definition from Richard Willis: The crystallized aggregates of atomic elements, morphologically distinguishable by 32 possible geometrical shapes (symmetry elements and their combinations) which in turn can be grouped into six crystal systems according to the complexity of their symmetries: isometric, hexagonal, tetragonal, orthorhombic, monoclinic, and triclinic. The aggregates (elements combined forming a given mineral) are determined by chemical bonding, which can occur electrostatically, electron-sharing, metallicazation, or residualization. Bonding effects hardness, density, solubility, melting point, tenacity, specific gravity, magnetism, structural properties, colors, etc. Subsequently, minerals can be classified into 11 groups according to chemical and physical properties: native elements, sulfides, sulfosalts, oxides and hydroxides, halides, carbonates, nitrates, borates, sulfates, phosphates, and silicates.

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    • (Glossary) Glass vs. Crystalline

      In ceramic technology the term 'glass' is contrast...

    • (Glossary) Water

      There is a need to discuss water in ceramic produc...

    • (Project) Ceramic Minerals Overview

      The materials we use are powders and we assess the...

    • (Tests) TRMN - Trace Minerals

    Pictures

    Some material data sheets show both the oxide and mineralogical analyses. Dolomite, for example, is composed of calcium carbonate and magnesium carbonate minerals, these can be separated mechanically. Although this material participates in the glaze melt to source the oxides, it's mineralogy specifically accounts for the unique way it decomposes and melts.

  • Mocha glazes

    Mocha diffusion is a technique of applying slips to ware so that one bleeds or diffuses into another. Typically oxides are mixed with tobacco juice and vinegar (e.g. apple cider works well) and a brush of the mix is touched to the surface of a coat of WET and freshly applied slip (i.e. Universal white slip).
  • Mole%

    Conceptually we consider fired glazes as being composed of 'oxides'. The ten major oxides likely make up 98% of all base glazes. The oxide formula of a glaze "explains" many details about the way the glaze fires. The relationship between a formula and the fired result is much more direct than between a recipe and the fired result. We can predict many fired properties and move individual properties in a specific direction by understanding what each oxide contributes and how they interact.

    Mole% is a way of expressing the oxide formula of a fired glaze or glass. It is one of the calculation types possible in Digitalfire Desktop Insight software, it has become popular as a way to rationalize formulas (and from these extrapolate fired properties like melting temperature, thermal expansion, hardness, resistance to leaching, etc). The Seger unity model is based on comparing numbers of oxides, it is about the dynamics of the way they interplay. This model is about knowing the concentration of individual oxides as a part of the whole. The Seger method of evaluating a glaze does not work as well at lower temperatures because some oxides that are powerful fluxes at high temperatures are refractory in low fire (dynamic reassignment of oxides to the Seger groups by temperature is not practical at this time). Thus oxides have a much more individual presence (at each temperature range) than the Seger method tends to recognize. Their contributions to particular properties often are not linear according to concentration. For example, boron is both a glass and a flux and the logic for its employment at various temperature ranges differs. It does not 'plug into' a Seger formula well.

    Mole% is simply a calculation of the percentage of oxide molecules by number (as opposed to an analysis which compares their weights). Following is an example of how to convert a raw formula to a Mole% formula.

               Raw                   Percent
    Oxides Formula Analysis
    -----------------------------------------
    K2O 0.6 / 12.1 x 100 = 5.0%
    CaO 1.3 / 12.1 x 100 = 10.7
    MgO 0.2 / 12.1 x 100 = 1.7
    ZnO 0.1 / 12.1 x 100 = 0.8
    Al2O3 0.9 / 12.1 x 100 = 7.4
    SiO2 9.0 / 12.1 x 100 = 74.3
    ----- -----
    Total 12.1 100.0


    Mole% ignores LOI (as do formulas), it just only looks at the oxides that makeup the fired glass. The target recipes that come with desktop INSIGHT include a few examples of Mole% target formulas from Richard Eppler.

    Out Bound Links

    • (Glossary) Unity Formula

      Conceptually we consider fired ceramic glazes as b...

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    • (Glossary) Analysis

      Conceptually we consider fired glazes as being com...

    • (Glossary) LOI

      Simplistically, LOI is the amount of weight a mate...

  • Monocottura, Monoporosa

    The single-firing process (as opposed to Bicottura which fires twice or more times) of making tile from terra cotta clay and firing it high enough to achieve a strong and dense product. Normally and engobe layer is applied over the body and glaze over that. The technique requires considerable expertise to develop a strong fired product (by virtue of crystal development in the matrix) and deal with the physical and thermal expansion matching of engobe and glaze to the body (and each other).

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  • Mottled

    See Variegated.
  • Mullite Crystals

    These grow in the porcelain matrix during firing and are a big reason why vitrified porcelain is so strong (the fired porcelain matrix is not just a bunch of silica particles glued together with feldspar glass, it has a complex structure, mullite is a key part of that). Mullite crystals are converted from kaolin particles and are long, producing a fibrous mesh.

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    • (Glossary) Fired Strength

      The fired strength of clays can be measured. The t...




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