| IUPAC name |
|Other names |
|E number||E551 (acidity regulators, ...)|
CompTox Dashboard (EPA)
|Molar mass||60.08 g/mol|
|Appearance||Transparent solid (Amorphous) White/Whitish Yellow (Powder/Sand)|
|Density||2.648 (α-quartz), 2.196 (amorphous) g·cm−3|
|Melting point||1,713 °C (3,115 °F; 1,986 K)(amorphous) (p4.88) to|
|Boiling point||2,950 °C (5,340 °F; 3,220 K)|
|Thermal conductivity||12 (|| c-axis), 6.8 (⊥ c-axis), 1.4 (am.) W/(m⋅K) (p12.213)|
Refractive index (nD)
|1.544 (o), 1.553 (e) (p4.143)|
|US health exposure limits (NIOSH):|
|TWA 20 mppcf (80 mg/m3/%SiO2) (amorphous)|
|TWA 6 mg/m3 (amorphous) |
Ca TWA 0.05 mg/m3
IDLH (Immediate danger)
|3000 mg/m3 (amorphous) |
Ca [25 mg/m3 (cristobalite, tridymite); 50 mg/m3 (quartz)]
| Carbon dioxide |
| Silicon monoxide |
Std enthalpy of
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Silicon dioxide, also known as silica, is an oxide of silicon with the chemical formula Si O 2, most commonly found in nature as quartz and in various living organisms.In many parts of the world, silica is the major constituent of sand. Silica is one of the most complex and most abundant families of materials, existing as a compound of several minerals and as synthetic product. Notable examples include fused quartz, fumed silica, silica gel, and aerogels. It is used in structural materials, microelectronics (as an electrical insulator), and as components in the food and pharmaceutical industries.
An oxide is a chemical compound that contains at least one oxygen atom and one other element in its chemical formula. "Oxide" itself is the dianion of oxygen, an O2– atom. Metal oxides thus typically contain an anion of oxygen in the oxidation state of −2. Most of the Earth's crust consists of solid oxides, the result of elements being oxidized by the oxygen in air or in water. Hydrocarbon combustion affords the two principal carbon oxides: carbon monoxide and carbon dioxide. Even materials considered pure elements often develop an oxide coating. For example, aluminium foil develops a thin skin of Al2O3 (called a passivation layer) that protects the foil from further corrosion. Individual elements can often form multiple oxides, each containing different amounts of the element and oxygen. In some cases these are distinguished by specifying the number of atoms as in carbon monoxide and carbon dioxide, and in other cases by specifying the element's oxidation number, as in iron(II) oxide and iron(III) oxide. Certain elements can form many different oxides, such as those of nitrogen. other examples are silicon, iron, titanium, and aluminium oxides.
Silicon is a chemical element with the symbol Si and atomic number 14. It is a hard and brittle crystalline solid with a blue-grey metallic lustre; and it is a tetravalent metalloid and semiconductor. It is a member of group 14 in the periodic table: carbon is above it; and germanium, tin, and lead are below it. It is relatively unreactive. Because of its high chemical affinity for oxygen, it was not until 1823 that Jöns Jakob Berzelius was first able to prepare it and characterize it in pure form. Its melting and boiling points of 1414 °C and 3265 °C respectively are the second-highest among all the metalloids and nonmetals, being only surpassed by boron. Silicon is the eighth most common element in the universe by mass, but very rarely occurs as the pure element in the Earth's crust. It is most widely distributed in dusts, sands, planetoids, and planets as various forms of silicon dioxide (silica) or silicates. More than 90% of the Earth's crust is composed of silicate minerals, making silicon the second most abundant element in the Earth's crust after oxygen.
A chemical formula is a way of presenting information about the chemical proportions of atoms that constitute a particular chemical compound or molecule, using chemical element symbols, numbers, and sometimes also other symbols, such as parentheses, dashes, brackets, commas and plus (+) and minus (−) signs. These are limited to a single typographic line of symbols, which may include subscripts and superscripts. A chemical formula is not a chemical name, and it contains no words. Although a chemical formula may imply certain simple chemical structures, it is not the same as a full chemical structural formula. Chemical formulas can fully specify the structure of only the simplest of molecules and chemical substances, and are generally more limited in power than are chemical names and structural formulas.
Inhaling finely divided crystalline silica is toxic and can lead to severe inflammation of the lung tissue, silicosis, bronchitis, lung cancer, and systemic autoimmune diseases, such as lupus and rheumatoid arthritis.
The lungs are the primary organs of the respiratory system in humans and many other animals including a few fish and some snails. In mammals and most other vertebrates, two lungs are located near the backbone on either side of the heart. Their function in the respiratory system is to extract oxygen from the atmosphere and transfer it into the bloodstream, and to release carbon dioxide from the bloodstream into the atmosphere, in a process of gas exchange. Respiration is driven by different muscular systems in different species. Mammals, reptiles and birds use their different muscles to support and foster breathing. In early tetrapods, air was driven into the lungs by the pharyngeal muscles via buccal pumping, a mechanism still seen in amphibians. In humans, the main muscle of respiration that drives breathing is the diaphragm. The lungs also provide airflow that makes vocal sounds including human speech possible.
Silicosis is a form of occupational lung disease caused by inhalation of crystalline silica dust. It is marked by inflammation and scarring in the form of nodular lesions in the upper lobes of the lungs. It is a type of pneumoconiosis. Silicosis is characterized by shortness of breath, cough, fever, and cyanosis. It may often be misdiagnosed as pulmonary edema, pneumonia, or tuberculosis.
Bronchitis is inflammation of the bronchi in the lungs that causes coughing. Symptoms include coughing up sputum, wheezing, shortness of breath, and chest pain. Bronchitis can be acute or chronic.
Inhalation of amorphous silicon dioxide, in high doses, leads to non-permanent short-term inflammation, where all effects heal.
Inhalation happens when air or other gases enter the lungs.
In condensed matter physics and materials science, an amorphous or non-crystalline solid is a solid that lacks the long-range order that is characteristic of a crystal. In some older books, the term has been used synonymously with glass. Nowadays, "glassy solid" or "amorphous solid" is considered to be the overarching concept, and glass the more special case: Glass is an amorphous solid that exhibits a glass transition. Polymers are often amorphous. Other types of amorphous solids include gels, thin films, and nanostructured materials such as glass.
In the majority of silicates, the silicon atom shows tetrahedral coordination, with four oxygen atoms surrounding a central Si atom. The most common example is seen in the quartz polymorphs. It is a 3 dimensional network solid in which each silicon atom is covalently bonded in a tetrahedral manner to 4 oxygen atoms.
In chemistry, a silicate is any member of a family of anions consisting of silicon and oxygen, usually with the general formula [SiO(4−2x)−
n, where 0 ≤ x < 2. The family includes orthosilicate SiO4−
4, metasilicate SiO2−
3, and pyrosilicate Si
7. The name is also used for any salt of such anions, such as sodium metasilicate; or any ester containing the corresponding chemical group, such as tetramethyl orthosilicate.
In materials science, polymorphism is the ability of a solid material to exist in more than one form or crystal structure. Polymorphism can potentially be found in any crystalline material including polymers, minerals, and metals, and is related to allotropy, which refers to chemical elements. The complete morphology of a material is described by polymorphism and other variables such as crystal habit, amorphous fraction or crystallographic defects. Polymorphism is relevant to the fields of pharmaceuticals, agrochemicals, pigments, dyestuffs, foods, and explosives.
For example, in the unit cell of α-quartz, the central tetrahedron shares all four of its corner O atoms, the two face-centered tetrahedra share two of their corner O atoms, and the four edge-centered tetrahedra share just one of their O atoms with other SiO4 tetrahedra. This leaves a net average of 12 out of 24 total vertices for that portion of the seven SiO4 tetrahedra that are considered to be a part of the unit cell for silica (see 3-D Unit Cell).
SiO2 has a number of distinct crystalline forms (polymorphs) in addition to amorphous forms. With the exception of stishovite and fibrous silica, all of the crystalline forms involve tetrahedral SiO4 units linked together by shared vertices in different arrangements. Silicon–oxygen bond lengths vary between the different crystal forms; for example in α-quartz the bond length is 161 pm, whereas in α-tridymite it is in the range 154–171 pm. The Si-O-Si angle also varies between a low value of 140° in α-tridymite, up to 180° in β-tridymite. In α-quartz, the Si-O-Si angle is 144°.
Stishovite is an extremely hard, dense tetragonal form (polymorph) of silicon dioxide. It is very rare on the Earth's surface, however, it may be a predominant form of silicon dioxide in the Earth, especially in the lower mantle.
Fibrous silica has a structure similar to that of SiS2 with chains of edge-sharing SiO4 tetrahedra. Stishovite, the higher-pressure form, in contrast, has a rutile-like structure where silicon is 6-coordinate. The density of stishovite is 4.287 g/cm3, which compares to α-quartz, the densest of the low-pressure forms, which has a density of 2.648 g/cm3. The difference in density can be ascribed to the increase in coordination as the six shortest Si-O bond lengths in stishovite (four Si-O bond lengths of 176 pm and two others of 181 pm) are greater than the Si-O bond length (161 pm) in α-quartz. The change in the coordination increases the ionicity of the Si-O bond. More importantly, any deviations from these standard parameters constitute microstructural differences or variations, which represent an approach to an amorphous, vitreous, or glassy solid.
The only stable form under normal conditions is alpha quartz, in which crystalline silicon dioxide is usually encountered. In nature, impurities in crystalline α-quartz can give rise to colors (see list). The high-temperature minerals, cristobalite and tridymite, have both lower densities and indices of refraction than quartz. Since the composition is identical, the reason for the discrepancies must be in the increased spacing in the high-temperature minerals. As is common with many substances, the higher the temperature, the farther apart the atoms are, due to the increased vibration energy.[ citation needed ]
The transformation from α-quartz to beta-quartz takes place abruptly at 573 °C. Since the transformation is accompanied by a significant change in volume, it can easily induce fracturing of ceramics or rocks passing through this temperature limit.
The high-pressure minerals, seifertite, stishovite, and coesite, though, have higher densities and indices of refraction than quartz. This is probably due to the intense compression of the atoms occurring during their formation, resulting in more condensed structure.
Faujasite silica is another form of crystalline silica. It is obtained by dealumination of a low-sodium, ultra-stable Y zeolite with combined acid and thermal treatment. The resulting product contains over 99% silica, and has high crystallinity and surface area (over 800 m2/g). Faujasite-silica has very high thermal and acid stability. For example, it maintains a high degree of long-range molecular order or crystallinity even after boiling in concentrated hydrochloric acid.
Molten silica exhibits several peculiar physical characteristics that are similar to those observed in liquid water: negative temperature expansion, density maximum at temperatures ~5000 °C, and a heat capacity minimum. Its density decreases from 2.08 g/cm3 at 1950 °C to 2.03 g/cm3 at 2200 °C.
Molecular SiO2 with a linear structure is produced when molecular silicon monoxide, SiO, is condensed in an argon matrix cooled with helium along with oxygen atoms generated by microwave discharge. Dimeric silicon dioxide, (SiO2)2 has been prepared by reacting O2 with matrix isolated dimeric silicon monoxide, (Si2O2). In dimeric silicon dioxide there are two oxygen atoms bridging between the silicon atoms with an Si-O-Si angle of 94° and bond length of 164.6 pm and the terminal Si-O bond length is 150.2 pm. The Si-O bond length is 148.3 pm, which compares with the length of 161 pm in α-quartz. The bond energy is estimated at 621.7 kJ/mol.
This section needs expansion. You can help by adding to it.(July 2017)
Silica with the chemical formula Si O 2 is most commonly found in nature as quartz, which comprises more than 10% by mass of the earth's crust.Quartz is the only polymorph of silica stable at the Earth's surface. Metastable occurrences of the high-pressure forms coesite and stishovite have been found around impact structures and associated with eclogites formed during ultra-high-pressure metamorphism. The high-temperature forms of tridymite and cristobalite are known from silica-rich volcanic rocks. In many parts of the world, silica is the major constituent of sand. . The various forms of silicon dioxide can be converted from one form to another by heating and changes in pressure.
Even though it is poorly soluble, silica occurs in many plants. Plant materials with high silica phytolith content appear to be of importance to grazing animals, from chewing insects to ungulates. Silica accelerates tooth wear, and high levels of silica in plants frequently eaten by herbivores may have developed as a defense mechanism against predation.
Silica is also the primary component of rice husk ash, which is used, for example, in filtration and cement manufacturing.
For well over a billion years, silicification in and by cells has been common in the biological world. In the modern world it occurs in bacteria, single-celled organisms, plants, and animals (invertebrates and vertebrates). Prominent examples include:
Crystalline minerals formed in the physiological 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 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 the cell wall of an organism (such as with phytoliths), or outside the cell wall, as typically happens with tests. Specific biochemical reactions exist for mineral deposition. Such reactions include those that involve lipids, proteins, and carbohydrates.
It is unclear in what ways silica is important in the nutrition of animals. This field of research is challenging because silica is ubiquitous and in most circumstances dissolves in trace quantities only. All the same it certainly does occur in the living body, leaving us with the problem that it is hard to create proper silica-free controls for purposes of research. This makes it difficult to be sure when the silica present has had operative beneficial effects, and when its presence is coincidental, or even harmful. The current consensus is that it certainly seems important in the growth, strength, and management of many connective tissues. This is true not only for hard connective tissues such as bone and tooth but possibly in the biochemistry of the subcellular enzyme-containing structures as well.
An estimated 95% of silicon dioxide (sand) produced is consumed in the construction industry, e.g. for the production of concrete (Portland cement concrete).
Silica, in the form of sand is used as the main ingredient in sand casting for the manufacture of metallic components in engineering and other applications. The high melting point of silica enables it to be used in such applications.
Crystalline silica is used in hydraulic fracturing of formations which contain tight oil and shale gas.
Silica is the primary ingredient in the production of most glass. The glass transition temperature of pure SiO2 is about 1475 K.When molten silicon dioxide SiO2 is rapidly cooled, it does not crystallize, but solidifies as a glass.
The structural geometry of silicon and oxygen in glass is similar to that in quartz and most other crystalline forms of silicon and oxygen with silicon surrounded by regular tetrahedra of oxygen centers. The difference between the glass and crystalline forms arises from the connectivity of the tetrahedral units: Although there is no long range periodicity in the glassy network ordering remains at length scales well beyond the SiO bond length. One example of this ordering is the preference to form rings of 6-tetrahedra.
Fumed silica also known as pyrogenic silica is a very fine particulate or colloidal form of silicon dioxide. It is prepared by burning SiCl4 in an oxygen-rich hydrogen flame to produce a "smoke" of SiO2.
The majority of optical fibers for telecommunication are also made from silica. It is a primary raw material for many ceramics such as earthenware, stoneware, and porcelain.
Silicon dioxide is used to produce elemental silicon. The process involves carbothermic reduction in an electric arc furnace:
Silica is a common additive in food production, where it is used primarily as a flow agent in powdered foods, or to adsorb water in hygroscopic applications. It is used as an anti-caking agent in powdered foods such as spices and non-dairy coffee creamer. It is the primary component of diatomaceous earth. Colloidal silica is also used as a wine, beer, and juice fining agent.It has the E number reference E551.
In pharmaceutical products, silica aids powder flow when tablets are formed.[ citation needed ]
In cosmetics, it is useful for its light-diffusing propertiesand natural absorbency.
Hydrated silica is used in toothpaste as a hard abrasive to remove tooth plaque.
Hydrophobic silica is used as a defoamer component.
In its capacity as a refractory, it is useful in fiber form as a high-temperature thermal protection fabric.[ citation needed ]
Silica is used in the extraction of DNA and RNA due to its ability to bind to the nucleic acids under the presence of chaotropes.
A silica-based aerogel was used in the Stardust spacecraft to collect extraterrestrial particles.
Pure silica (silicon dioxide), when cooled as fused quartz into a glass with no true melting point, can be used as a glass fiber for fiberglass.
Silicon dioxide is mostly obtained by mining, including sand mining and purification of quartz. Quartz is suitable for many purposes, while chemical processing is required to make a purer or otherwise more suitable (e.g. more reactive or fine-grained) product.[ citation needed ]
Silica fume is obtained as byproduct from hot processes like ferrosilicon production. It is less pure than fumed silica and should not be confused with that product. The production process, particle characteristics and fields of application of fumed silica are all different from those of silica fume.
Precipitated silica or amorphous silica is produced by the acidification of solutions of sodium silicate. The gelatinous precipitate or silica gel, is first washed and then dehydrated to produce colorless microporous silica.The idealized equation involving a trisilicate and sulfuric acid is:
Approximately one billion kilograms/year (1999) of silica were produced in this manner, mainly for use for polymer composites – tires and shoe soles.
Thin films of silica grow spontaneously on silicon wafers via thermal oxidation, producing a very shallow layer of about 1 nm or 10 Å of so-called native oxide. °C, using so-called dry or wet oxidation with O2Higher temperatures and alternative environments are used to grow well-controlled layers of silicon dioxide on silicon, for example at temperatures between 600 and 1200
or H2O, respectively.
The native oxide layer is beneficial in microelectronics, where it acts as electric insulator with high chemical stability. It can protect the silicon, store charge, block current, and even act as a controlled pathway to limit current flow.
Many routes to silicon dioxide start with an organosilicon compound, e.g., HMDSO °C results in the oxide:, TEOS. Synthesis of silica is illustrated below using tetraethyl orthosilicate (TEOS). Simply heating TEOS at 680–730
Similarly TEOS combusts around 400 °C:
TEOS undergoes hydrolysis via the so-called sol-gel process. The course of the reaction and nature of the product are affected by catalysts, but the idealized equation is:
Being highly stable, silicon dioxide arises from many methods. Conceptually simple, but of little practical value, combustion of silane gives silicon dioxide. This reaction is analogous to the combustion of methane:
However the chemical vapor deposition of silicon dioxide onto crystal surface from silane had been used using nitrogen as a carrier gas at 200–500 °C.
Silica is converted to silicon by reduction with carbon.
Fluorine reacts with silicon dioxide to form SiF4 and O2 whereas the other halogen gases (Cl2, Br2, I2) are essentially unreactive.
Silicon dioxide is attacked by hydrofluoric acid (HF) to produce hexafluorosilicic acid:
HF is used to remove or pattern silicon dioxide in the semiconductor industry.
Under normal conditions, silicon does not react with most acids but is dissolved by hydrofluoric acid.
Silicon is attacked by bases such as aqueous sodium hydroxide to give silicates.
Silicon dioxide acts as a Lux–Flood acid, being able to react with bases under certain conditions. As it does not contain any hydrogen, it cannot act as a Brønsted–Lowry acid. While not soluble in water, some strong bases will react with glass and have to be stored in plastic bottles as a result.
Silicon dioxide dissolves in hot concentrated alkali or fused hydroxide, as described in this idealized equation:
Silicon dioxide will neutralise basic metal oxides (e.g. sodium oxide, potassium oxide, lead(II) oxide, zinc oxide, or mixtures of oxides, forming silicates and glasses as the Si-O-Si bonds in silica are broken successively).As an example the reaction of sodium oxide and SiO2 can produce sodium orthosilicate, sodium silicate, and glasses, dependent on the proportions of reactants:
Examples of such glasses have commercial significance, e.g. soda-lime glass, borosilicate glass, lead glass. In these glasses, silica is termed the network former or lattice former.The reaction is also used in blast furnaces to remove sand impurities in the ore by neutralisation with calcium oxide, forming calcium silicate slag.
Silicon dioxide reacts in heated reflux under dinitrogen with ethylene glycol and an alkali metal base to produce highly reactive, pentacoordinate silicates which provide access to a wide variety of new silicon compounds.The silicates are essentially insoluble in all polar solvent except methanol.
Silicon dioxide reacts with elemental silicon at high temperatures to produce SiO:
The solubility of silicon dioxide in water strongly depends on its crystalline form and is three-four times higher for silica[ clarification needed ] than quartz; as a function of temperature, it peaks around 340 °C. This property is used to grow single crystals of quartz in a hydrothermal process where natural quartz is dissolved in superheated water in a pressure vessel that is cooler at the top. Crystals of 0.5–1 kg can be grown over a period of 1–2 months. These crystals are a source of very pure quartz for use in electronic applications.
Silica ingested orally is essentially nontoxic, with an LD50 of 5000 mg/kg (5 g/kg). A 2008 study following subjects for 15 years found that higher levels of silica in water appeared to decrease the risk of dementia. An increase of 10 mg/day of silica in drinking water was associated with a decreased risk of dementia of 11%.
Inhaling finely divided crystalline silica dust can lead to silicosis, bronchitis, or lung cancer, as the dust becomes lodged in the lungs and continuously irritates the tissue, reducing lung capacities.When fine silica particles are inhaled in large enough quantities (such as through occupational exposure), it increases the risk of systemic autoimmune diseases such as lupus and rheumatoid arthritis compared to expected rates in the general population.
Silica is an occupational hazard for people who do sandblasting, or work with products that contain powdered crystalline silica. Amorphous silica, such as fumed silica, may cause irreversible lung damage in some cases, but is not associated with development of silicosis. Children, asthmatics of any age, those with allergies, and the elderly (all of whom have reduced lung capacity) can be affected in less time.
Crystalline silica is an occupational hazard for those working with stone countertops, because the process of cutting and installing the countertops creates large amounts of airborne silica.Crystalline silica used in hydraulic fracturing presents a health hazard to workers.
In the body, crystalline silica particles do not dissolve over clinically relevant periods. Silica crystals inside the lungs can activate the NLRP3 inflammasome inside macrophages and dendritic cells and thereby result in production of interleukin, a highly pro-inflammatory cytokine in the immune system.
Regulations restricting silica exposure 'with respect to the silicosis hazard' specify that they are concerned only with silica, which is both crystalline and dust-forming.
In 2013, the U.S. Occupational Safety and Health Administration reduced the exposure limit to 50 µg/m3 of air. Prior to 2013, it had allowed 100 µg/m3 and in construction workers even 250 µg/m3. In 2013, OSHA also required "green completion" of fracked wells to reduce exposure to crystalline silica besides restricting the limit of exposure.
SiO2, more so than almost any material, exists in many crystalline forms. These forms are called polymorphs.
Pearson symbol, group No.
|α-quartz|| rhombohedral (trigonal)|
hP9, P3121 No.152
|2.648||Helical chains making individual single crystals optically active; α-quartz converts to β-quartz at 846 K|
|β-quartz|| hexagonal |
hP18, P6222, No. 180
|2.533||Closely related to α-quartz (with an Si-O-Si angle of 155°) and optically active; β-quartz converts to β-tridymite at 1140 K|
|α-tridymite|| orthorhombic |
oS24, C2221, No.20
|2.265||Metastable form under normal pressure|
hP12, P63/mmc, No. 194
|Closely related to α-tridymite; β-tridymite converts to β-cristobalite at 2010 K|
|α-cristobalite|| tetragonal |
tP12, P41212, No. 92
|2.334||Metastable form under normal pressure|
|β-cristobalite|| cubic |
cF104, Fd3m, No.227
|Closely related to α-cristobalite; melts at 1978 K|
tP36, P41212, No. 92
|3.011||Si5O10, Si4O8, Si8O16 rings; synthesised from glassy silica and alkali at 600–900 K and 40–400 MPa|
|moganite|| monoclinic |
mS46, C2/c, No.15
|Si4O8 and Si6O12 rings|
mS48, C2/c, No.15
|2.911||Si4O8 and Si8O16 rings; 900 K and 3–3.5 GPa|
tP6, P42/mnm, No.136
|4.287||One of the densest (together with seifertite) polymorphs of silica; rutile-like with 6-fold coordinated Si; 7.5–8.5 GPa|
|4.294||One of the densest (together with stishovite) polymorphs of silica; is produced at pressures above 40 GPa.|
|melanophlogite||cubic (cP*, P4232, No.208) or tetragonal (P42/nbc)||2.04||Si5O10, Si6O12 rings; mineral always found with hydrocarbons in interstitial spaces - a clathrasil|
oI12, Ibam, No.72
|1.97||Like SiS2 consisting of edge sharing chains, melts at ~1700 K|
|2D silica||hexagonal||Sheet-like bilayer structure|
Kaolinite is a clay mineral, part of the group of industrial minerals with the chemical composition Al2Si2O5(OH)4. It is a layered silicate mineral, with one tetrahedral sheet of silica (SiO
4) linked through oxygen atoms to one octahedral sheet of alumina (AlO
6) octahedra. Rocks that are rich in kaolinite are known as kaolin or china clay.
Aluminium oxide (IUPAC name) or aluminum oxide (American English) is also known as Alumina. It is a chemical compound of aluminium and oxygen with the chemical formula Al2O3. It is the most commonly occurring of several aluminium oxides, and specifically identified as aluminium(III) oxide. It is commonly called alumina and may also be called aloxide, aloxite, or alundum depending on particular forms or applications. It occurs naturally in its crystalline polymorphic phase α-Al2O3 as the mineral corundum, varieties of which form the precious gemstones ruby and sapphire. Al2O3 is significant in its use to produce aluminium metal, as an abrasive owing to its hardness, and as a refractory material owing to its high melting point.
Silane is an inorganic compound with chemical formula, SiH4, making it a group 14 hydride. It is a colourless, pyrophoric gas with a sharp, repulsive smell, somewhat similar to that of acetic acid. Silane is of practical interest as a precursor to elemental silicon.
Magnesium carbonate, MgCO3 (archaic name magnesia alba), is an inorganic salt that is a white solid. Several hydrated and basic forms of magnesium carbonate also exist as minerals.
Cristobalite is a mineral polymorph of silica that is formed at very high-temperatures. It is used in dentistry as a component of alginate impression materials as well as for making models of teeth
Coesite is a form (polymorph) of silicon dioxide SiO2 that is formed when very high pressure (2–3 gigapascals), and moderately high temperature (700 °C, 1,300 °F), are applied to quartz. Coesite was first synthesized by Loring Coes Jr., a chemist at the Norton Company, in 1953.
Silicate minerals are rock-forming minerals made up of silicate groups. They are the largest and most important class of minerals and make up approximately 90 percent of the Earth's crust.
Boron trioxide (or diboron trioxide) is one of the oxides of boron. It is a white, glassy solid with the formula B2O3. It is almost always found as the vitreous (amorphous) form; however, it can be crystallized after extensive annealing (that is, under prolonged heat).
Germanium dioxide, also called germanium oxide, germania, and salt of germanium, is an inorganic compound with the chemical formula GeO2. It is the main commercial source of germanium. It also forms as a passivation layer on pure germanium in contact with atmospheric oxygen.
Tetraethyl orthosilicate, formally named tetraethoxysilane and abbreviated TEOS, is the chemical compound with the formula Si(OC2H5)4. TEOS is a colorless liquid that degrades in water. TEOS is the ethyl ester of orthosilicic acid, Si(OH)4. It is the most prevalent alkoxide of silicon.
Silicon monoxide is the chemical compound with the formula SiO where silicon is present in the oxidation state +2. In the vapour phase it is a diatomic molecule. It has been detected in stellar objects and it has been described as the most common oxide of silicon in the universe.
When SiO gas is cooled rapidly, it condenses to form a brown/black polymeric glassy material, (SiO)n, which is available commercially and used to deposit films of SiO. Glassy (SiO)n is air- and moisture-sensitive. Its surface readily oxidizes in air at room temperature, giving an SiO2 surface layer that protects the material from further oxidation. However, (SiO)n irreversibly disproportionates into SiO2 and Si in a few hours between 400 and 800°C, and very rapidly between 1,000 and 1,440°C, although the reaction does not go to completion.
The glass–liquid transition, or glass transition, is the gradual and reversible transition in amorphous materials, from a hard and relatively brittle "glassy" state into a viscous or rubbery state as the temperature is increased. An amorphous solid that exhibits a glass transition is called a glass. The reverse transition, achieved by supercooling a viscous liquid into the glass state, is called vitrification.
The structure of liquids, glasses and other non-crystalline solids is characterized by the absence of long-range order which defines crystalline materials. Liquids and amorphous solids do, however, possess a rich and varied array of short to medium range order, which originates from chemical bonding and related interactions. Metallic glasses, for example, are typically well described by the dense random packing of hard spheres, whereas covalent systems, such as silicate glasses, have sparsely packed, strongly bound, tetrahedral network structures. These very different structures result in materials with very different physical properties and applications.
Silicon oxynitride is a ceramic material with the chemical formula SiOxNy. While in amorphous forms its composition can continuously vary between SiO2 (silica) and Si3N4 (silicon nitride), the only known intermediate crystalline phase is Si2N2O. It is found in nature as the rare mineral sinoite in some meteorites and can be synthesized in the laboratory.
Mineral alteration refers to the various natural processes that alter a mineral's chemical composition or crystallography.
These soft focus pigments, mainly composed of polymers, micas and talcs covered with rough or spherical particles of small diameters, such as silica or titanium dioxide, are used to optically reduce the appearance of wrinkles. These effects are obtained by optimizing outlines of wrinkles and reducing the difference of brightness due to diffuse reflection.
The silica is a multiporous ingredient, which absorbs the oil and sebum.
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