Pure silicon dioxide
|Jmol-3D images||Image 1|
|Molar mass||60.08 g/mol|
|Melting point||1,600 to 1,725 °C (2,912 to 3,137 °F; 1,873 to 1,998 K)|
|Boiling point||2,230 °C (4,050 °F; 2,500 K)|
|Related diones||Carbon dioxide
|Related compounds||Silicon monoxide
|Std enthalpy of
|Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)|
|(what is: / ?)|
Silicon dioxide, also known as silica (from the Latin silex), is a chemical compound that is an oxide of silicon with the chemical formula SiO2. It has been known since ancient times. Silica is most commonly found in nature as quartz, as well as in various living organisms, Silica is one of the most complex and most abundant families of materials, existing both as several minerals and being produced synthetically. Notable examples include fused quartz, crystal, fumed silica, silica gel, and aerogels. Applications range from structural materials to microelectronics to components used in the food industry.
- 1 Production
- 2 Uses
- 3 Structure
- 4 Fused quartz
- 5 Chemical reactions
- 6 Occurrence
- 7 Health effects
- 8 Crystalline forms of silicon dioxide
- 9 See also
- 10 References
- 11 External links
Silicon dioxide is obtained by mining and purification of the resulting mineral. Quartz comprises more than 10% by mass of the earth's crust. Commercial silicon dioxide is also produced, almost always via the processing of quartz, synthetically on a very large scale.
Amorphous silica, silica gel, is produced by the acidification of solutions of sodium silicate. An initially formed gelatinous precipitate is then washed and then dehydrated to produce colorless microporous silica. Ideallized equation involving a trisilicate and sulfuric acid is shown:
- Na2Si3O7 + H2SO4 → 3 SiO2 + Na2SO4 + H2O
Approximately one billion kilograms/year (1999) of silica was 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. This route gives a very shallow layer (approximately 1 nm or 10 Å) of so-called native oxide. Higher temperatures and alternative environments are used to grow well-controlled layers of silicon dioxide on silicon, for example at temperatures between 600 and 1200 °C, using so-called dry or wet oxidation with O2 or H2O, respectively. The depth of the layer of silicon replaced by the dioxide is 44% of the depth of the silicon dioxide layer produced.
The native oxide layer can be beneficial in microelectronics, where it acts as electric insulators with high chemical stability. In electrical applications, it can protect the silicon, store charge, block current, and even act as a controlled pathway to limit current flow.
Laboratory or specialty methods
From silicate esters
Many routes to silicon dioxide start with silicate esters, the best known being tetraethyl orthosilicate (TEOS). Simply heating TEOS at 680–730 °C gives the dioxide:
- Si(OC2H5)4 → SiO2 + 2 O(C2H5)2
Similarly TEOS combusts around 400 °C:
- Si(OC2H5)4 + 12 O2 → SiO2 + 10 H2O + 8 CO2
- Si(OC2H5)4 + 2 H2O → SiO2 + 4 HOCH2CH3
Being highly stable, silicon dioxide arises from many methods. Conceptually simple, but of little practical value, combustion of silane give silicon dioxide. This reaction is analogous to the combustion of methane:
- SiH4 + 2 O2 → SiO2 + 2 H2O.
Precursor to glass and silicon metal
Silica is used primarily in the production of glass for windows, drinking glasses, beverage bottles, and many other uses. 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.
- SiO2 + 2 C → Si + 2 CO
Food and pharmaceutical applications
Silica is a common additive in the production of foods, where it is used primarily as a flow agent in powdered foods, or to absorb water in hygroscopic applications. It is the primary component of diatomaceous earth. Colloidal silica is also used as a wine, beer, and juice fining agent.
In pharmaceutical products, silica aids powder flow when tablets are formed.
A silica-based aerogel was used in the Stardust spacecraft to collect extraterrestrial particles. Silica is also used in the extraction of DNA and RNA due to its ability to bind to the nucleic acids under the presence of chaotropes. As hydrophobic silica it is used as a defoamer component. In hydrated form, it is used in toothpaste as a hard abrasive to remove tooth plaque.
In its capacity as a refractory, it is useful in fiber form as a high-temperature thermal protection fabric. In cosmetics, it is useful for its light-diffusing properties and natural absorbency. It is also used as a thermal enhancement compound in ground source heat pump industry.
In the majority of silicates, the Si atom shows tetrahedral coordination, with 4 oxygen atoms surrounding a central Si atom. The most common example is seen in the quartz crystalline form of silica SiO2. In each of the most thermodynamically stable crystalline forms of silica, on average, all 4 of the vertices (or oxygen atoms) of the SiO4 tetrahedra are shared with others, yielding the net chemical formula: SiO2.
For example, in the unit cell of α-quartz, the central tetrahedron shares all 4 of its corner O atoms, the 2 face-centered tetrahedra share 2 of their corner O atoms, and the 4 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 7 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°.
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. But more important is the observation that 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 α-quartz and this is the form 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 a lower density and index 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 due to the increased vibration energy.
The high pressure minerals, seifertite, stishovite, and coesite, on the other hand, have a higher density and index of refraction when compared to quartz. This is probably due to the intense compression of the atoms that must occur during their formation, resulting in a 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 a combined acid and thermal treatment. The resulting product contains over 99% silica, has high crystallinity and high 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 the ones 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. When molecular silicon monoxide, SiO, is condensed in an argon matrix cooled with helium along with oxygen atoms generated by microwave discharge, molecular SiO2 is produced with a linear structure. 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.
When molten silicon dioxide SiO2 is rapidly cooled, it does not crystallize but solidifies as a glass. The geometry of the silicon and oxygen centers in glass is similar to that in quartz and most other crystalline forms of the same composition, i.e., silicon is surrounded by a regular tetrahedra of oxygen centers. The difference between the glass and the crystalline forms arise from the connectivity of these tetrahedral units. Although there is no long range periodicity in the glassy network there remains significant ordering at length scales well beyond the SiO bond length. One example of this ordering is found in the preference of the network to form rings of 6-tetrahedra.
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.
- SiO2 + 6 HF → H2SiF6 + 2 H2O.
HF is used to remove or pattern silicon dioxide in the semiconductor industry.
Silicon dioxide dissolves in hot concentrated alkali or fused hydroxide, as described in this idealized equation:
- SiO2 + 2 NaOH → Na2SiO3 + H2O.
Silicon dioxide reacts with 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:
- 2 Na2O + SiO2 → Na4SiO4;
- Na2O + SiO2 → Na2SiO3;
- (0.25–0.8)Na2O + SiO2 → glass.
Silicon dioxide reacts with elemental silicon at high temperatures to produce SiO:
- SiO2 + Si → 2 SiO
Solubility in water
The solubility of silicon dioxide in water strongly depends on its crystalline form and is 3–4 times higher for silica than quartz; as a function of temperature, it peaks at about 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.
Even though it is poorly soluble, silica occurs widely in many plants. Plant materials with high silica phytolith content appear to be of importance to grazing animals, from chewing insects to ungulates. Studies have shown that it accelerates tooth wear, and high levels of silica in plants frequently eaten by herbivores may have developed as a defense mechanism against predation.
It is also the primary component of rice husk ash, which is used, for example, in filtration and cement manufacturing.
Silicification in and by cells has been common in the biological world for well over a billion years. In the modern world it occurs in bacteria, single-celled organisms, plants, and animals (invertebrates and vertebrates). Prominent examples include:
- Tests or frustules of diatoms and Radiolaria.
- Silica phytoliths in the cells of many plants, including Equisetaceae, practically all grasses, and a wide range of dicotyledons.
- The spicules forming the skeleton of many sponges.
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 animal. 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.
Silica ingested orally is essentially nontoxic, with an LD50 of 5000 mg/kg. On the other hand, inhaling finely divided crystalline silica dust can lead to silicosis, bronchitis, or cancer, as the dust becomes lodged in the lungs and continuously irritates them, reducing lung capacities. Studies of workers with exposure to crystalline silica have shown 10-fold higher than expected rates of lupus and other systemic autoimmune diseases compared to expected rates in the general population. Prior to new rules issued in 2013, OSHA allowed 100 µg per cubic meter of air. The new regulations reduce the amount to 50 µg/m3 down from 100 µg/m3. The exposure limit for the construction industry is also set at 50 µg/m3 down from 250 µg/m3.
In the body crystalline silica particles do not dissolve over clinically relevant periods. Silica crystals can activate the NLRP3 inflammasome inside macrophages and dendritic cells and thereby result in processing of pro-Interleukin 1 beta into its mature form. Chronic exposure to silica may thereby account for some of its health hazards, as interleukin-1 is a highly pro-inflammatory cytokine in the immune system. This effect can create an occupational hazard for people working with sandblasting equipment, products that contain powdered crystalline silica and so on. Children, asthmatics of any age, allergy sufferers, and the elderly (all of whom have reduced lung capacity) can be affected in much less time. Amorphous silica, such as fumed silica is not associated with development of silicosis, but may cause irreversible lung damage in some cases. Laws restricting silica exposure with respect to the silicosis hazard specify that they are concerned only with silica that is both crystalline and dust-forming.
A study that followed subjects for 15 years found that higher levels of silica in water appeared to decrease the risk of dementia. The study found an association between an increase of 10 milligram-per-day of the intake of silica in drinking water with a decreased risk of dementia of 11%.
Crystalline silica is used in hydraulic fracturing of formation which contain tight oil and shale gas, a use which presents a health hazard to workers. In 2013 OSHA announced tightened restrictions on the amount of crystalline silica which could be present and required "green completion" of fracked wells to reduce exposure.
Crystalline forms of silicon dioxide
SiO2, more so than almost any material, exists in many crystalline forms (called polymorphs).
Pearson symbol, group No.
hP9, P3121 No.152
|2.648||Helical chains making individual single crystals optically active; α-quartz converts to β-quartz at 846 K|
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|
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|
tP12, P41212, No. 92
|2.334||metastable form under normal pressure|
cF104, Fd3m, No.227
|closely related to α-cristobalite; melts at 1978 K|
cF576, Fd3m, No.227
|1.92||sodalite cages connected by hexagonal prisms; 12-membered ring pore opening; faujasite structure.|
|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|
tP36, P41212, No. 92
|3.011||Si5O10, Si4O14, Si8O16 rings; synthesised from glassy silica and alkali at 600–900 K and 40–400 MPa|
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|
oI12, Ibam, No.72
|1.97||like SiS2 consisting of edge sharing chains, melts at ~1700 K|
|4.294||One of the densest (together with stishovite) polymorphs of silica; is produced at pressures above 40 GPa.|
- Zumdahl, Steven S. (2009). Chemical Principles 6th Ed. Houghton Mifflin Company. p. A22. ISBN 0-618-94690-X.
- Iler, R. K. (1979). The Chemistry of Silica. Plenum Press. ISBN 0-471-02404-X.
- Flörke, Otto W. et al. (2008) "Silica" in Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, . doi:10.1002/14356007.a23_583.pub3.
- Greenwood, Norman N.; Earnshaw, Alan (1984). Chemistry of the Elements. Oxford: Pergamon Press. pp. 393–99. ISBN 0-08-022057-6.
- Doering, Robert and Nishi, Yoshio (2007). Handbook of Semiconductor Manufacturing Technology. CRC Press. ISBN 1-57444-675-4.
- Lee, Sunggyu (2006). Encyclopedia of chemical processing. CRC Press. ISBN 0-8247-5563-4.
- Riordan, Michael (2007) "The Silicon Dioxide Solution: How physicist Jean Hoerni built the bridge from the transistor to the integrated circuit" IEEE Spectrum.
- Nandiyanto, A. B. D.; Kim, S. G.; Iskandar, F.; Okuyama, K. (2009). "Synthesis of spherical mesoporous silica nanoparticles with nanometer-size controllable pores and outer diameters". Microporous and Mesoporous Materials 120 (3): 447. doi:10.1016/j.micromeso.2008.12.019.
- Shriver and Atkins. Inorganic Chemistry (5th Edition). W. H. Freeman and Company, New York, 2010, p. 354.
- Skinner B. J., Appleman D. E. (1963). "Melanophlogite, a cubic polymorph of silica". American Mineralogist 48: 854–867.
- Holleman, A. F.; Wiberg, E. (2001), Inorganic Chemistry, San Diego: Academic Press, ISBN 0-12-352651-5
- Wells A. F. (1984). Structural Inorganic Chemistry. Oxford Science Publications. ISBN 0-19-855370-6.
- Kirfel, A.; Krane, H. G.; Blaha, P.; Schwarz, K.; Lippmann, T. (2001). "Electron-density distribution in stishovite, SiO2: a new high-energy synchrotron-radiation study". Acta Crystallographica A 57 (6): 663. doi:10.1107/S0108767301010698.
- Scherzer, J. (1978). "Dealuminated faujasite-type structures with SiO2/Al2O3 ratios over 100". Journal of Catalysis 54 (2): 285. doi:10.1016/0021-9517(78)90051-9.
- Shell, Scott M.; Debenedetti, Pablo G. and Panagiotopoulos, Athanassios Z. (2002). "Molecular structural order and anomalies in liquid silica". Phys. Rev. E 66: 011202. arXiv:cond-mat/0203383. Bibcode:2002PhRvE..66a1202S. doi:10.1103/PhysRevE.66.011202.
- Aksay, I. A.; Pask, J. A. and Davis, R. F. (1979). "Densities of SiO2-Al2O3 Melts". Journal of the American Ceramic Society 62 (7–8): 332–336. doi:10.1111/j.1151-2916.1979.tb19071.x.
- Jutzi, Peter and Schubert, Ulrich (2003). Silicon chemistry: from the atom to extended systems. Wiley-VCH. ISBN 3-527-30647-1.
- Elliott, S. R. (1991). "Medium-range structural order in covalent amorphous solids". Nature 354 (6353): 445–452. Bibcode:1991Natur.354..445E. doi:10.1038/354445a0.
- Ojovan, M. I. (2004). "Glass formation in amorphous SiO2 as a percolation phase transition in a system of network defects". Journal of Experimental and Theoretical Physics Letters 79 (12): 632–634. Bibcode:2004JETPL..79..632O. doi:10.1134/1.1790021.
- Fournier R. O., Rowe J. J. (1977). "The solubility of amorphous silica in water at high temperatures and high pressures". American Mineralogist 62: 1052–1056.
- Massey, Fergus P.; Ennos, A. Roland; Hartley, Sue E. (2006). "Silica in grasses as a defence against insect herbivores: Contrasting effects on folivores and a phloem feeder". Journal of Animal Ecology 75 (2): 595–603. doi:10.1111/j.1365-2656.2006.01082.x. PMID 16638012.
- Keeping, Malcolm G.; Kvedaras, Olivia L. (2008). "Silicon as a plant defence against insect herbivory: Response to Massey, Ennos and Hartley". Journal of Animal Ecology 77 (3): 631–3. doi:10.1111/j.1365-2656.2008.01380.x. PMID 18341561.
- Carlisle, EM (1986). "Silicon as an essential trace element in animal nutrition". Ciba Foundation symposium. Novartis Foundation Symposia 121: 123–39. doi:10.1002/9780470513323.ch8. ISBN 978-0-470-51332-3. PMID 3743227.
- CPWR-Center for Construction Research and Training — Work Safely with Silica: "What are the Health Effects? http://www.silica-safe.org
- Greenhouse, Steven (August 23, 2013). "New Rules Would Cut Silica Dust Exposure". The New York Times. Retrieved August 24, 2013.
- Hornung, Veit; Bauernfeind, Franz; Halle, Annett; Samstad, Eivind O.; Kono, Hajime; Rock, Kenneth L.; Fitzgerald, Katherine A.; Latz, Eicke (2008). "Silica crystals and aluminum salts activate the NALP3 inflammasome through phagosomal destabilization". Nature Immunology 9 (8): 847–856. doi:10.1038/ni.1631. PMC 2834784. PMID 18604214.
- NIOSH (1986) Occupational respiratory diseases. Cincinnati, OH: U.S. Department of Health and Human Services, U.S. Public Health Service, Centers for Disease Control, National Institute for Occupational Safety and Health, DHHS (NIOSH) Publication No. 86-102.
- NIOSH (2002) Hazard Review, Health Effects of Occupational Exposure to Respirable Crystalline Silica. Cincinnati, OH: U.S. Department of Health and Human Services, U.S. Public Health Service, Centers for Disease Control, National Institute for Occupational Safety and Health, DHHS (NIOSH) Publication No. 2002-129.
- Reuzel, P. G.; Bruijntjes, J. P.; Feron, V. J.; Woutersen, R. A. (1991). "Subchronic inhalation toxicity of amorphous silicas and quartz dust in rats". Food and Chemical Toxicology 29 (5): 341–54. doi:10.1016/0278-6915(91)90205-L. PMID 1648030.
- Rondeau, V.; Jacqmin-Gadda, H.; Commenges, D.; Helmer, C.; Dartigues, J.-F. (2008). "Aluminum and Silica in Drinking Water and the Risk of Alzheimer's Disease or Cognitive Decline: Findings from 15-Year Follow-up of the PAQUID Cohort". American Journal of Epidemiology 169 (4): 489–96. doi:10.1093/aje/kwn348. PMC 2809081. PMID 19064650.
- Lager G. A., Jorgensen J. D., Rotella F.J. (1982). "Crystal structure and thermal expansion of a-quartz SiO2 at low temperature". Journal of Applied Physics 53 (10): 6751–6756. Bibcode:1982JAP....53.6751L. doi:10.1063/1.330062.
- Wright, A. F.; Lehmann, M. S. (1981). "The structure of quartz at 25 and 590 °C determined by neutron diffraction". Journal of Solid State Chemistry 36 (3): 371–80. Bibcode:1981JSSCh..36..371W. doi:10.1016/0022-4596(81)90449-7.
- Kihara, Kuniaki; Matsumoto, Takeo; Imamura, Moritaka (1986). "Structural change of orthorhombic-Itridymite with temperature: A study based on second-order thermal-vibrational parameters". Zeitschrift für Kristallographie 177: 27–38. Bibcode:1986ZK....177...27K. doi:10.1524/zkri.1986.177.1-2.27.
- Downs R. T., Palmer D. C. (1994). "The pressure behavior of a cristobalite". American Mineralogist 79: 9–14.
- Wright, A. F.; Leadbetter, A. J. (1975). "The structures of the β-cristobalite phases of SiO2 and AlPO4". Philosophical Magazine 31 (6): 1391–401. Bibcode:1975PMag...31.1391W. doi:10.1080/00318087508228690.
- Hriljac, J. A.; Eddy, M. M.; Cheetham, A. K.; Donohue, J. A.; Ray, G. J. (1993). "Powder Neutron Diffraction and 29Si MAS NMR Studies of Siliceous Zeolite-Y". Journal of Solid State Chemistry 106: 66–72. Bibcode:1993JSSCh.106...66H. doi:10.1006/jssc.1993.1265.
- Nakagawa T., Kihara K., Harada K. (2001). "The crystal structure of low melanophlogite". American Mineralogist 86: 1506.
- Rosemarie Szostak (1998). Molecular sieves: Principles of Synthesis and Identification. Springer. ISBN 0-7514-0480-2.
- Shropshire, Joseph; Keat, Paul P.; Vaughan, Philip A. (1959). "The crystal structure of keatite, a new form of silica". Zeitschrift für Kristallographie 112: 409–13. Bibcode:1959ZK....112..409S. doi:10.1524/zkri.1959.112.1-6.409.
- Miehe, Gerhard; Graetsch, Heribert (1992). "Crystal structure of moganite: a new structure type for silica". European Journal of Mineralogy 4: 693–706.
- Levien L., Prewitt C. T. (1981). "High-pressure crystal structure and compressibility of coesite". American Mineralogist 66: 324–333.
- Smyth J. R., Swope R. J., Pawley A. R. (1995). "H in rutile-type compounds: II. Crystal chemistry of Al substitution in H-bearing stishovite". American Mineralogist 80: 454–456.
- Weiss, Alarich; Weiss, Armin (1954). "Über Siliciumchalkogenide. VI. Zur Kenntnis der faserigen Siliciumdioxyd-Modifikation". Zeitschrift für anorganische und allgemeine Chemie 276: 95–112. doi:10.1002/zaac.19542760110.
- Dera P., Prewitt C. T., Boctor N. Z., Hemley R. J. (2002). "Characterization of a high-pressure phase of silica from the Martian meteorite Shergotty". American Mineralogist 87: 1018.
- Seifertite. Mindat.org.