WO2009029263A1 - Refractory glass ceramics - Google Patents
Refractory glass ceramics Download PDFInfo
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- WO2009029263A1 WO2009029263A1 PCT/US2008/010133 US2008010133W WO2009029263A1 WO 2009029263 A1 WO2009029263 A1 WO 2009029263A1 US 2008010133 W US2008010133 W US 2008010133W WO 2009029263 A1 WO2009029263 A1 WO 2009029263A1
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C10/00—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition
- C03C10/0036—Devitrified glass ceramics, i.e. glass ceramics having a crystalline phase dispersed in a glassy phase and constituting at least 50% by weight of the total composition containing SiO2, Al2O3 and a divalent metal oxide as main constituents
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- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B32/00—Thermal after-treatment of glass products not provided for in groups C03B19/00, C03B25/00 - C03B31/00 or C03B37/00, e.g. crystallisation, eliminating gas inclusions or other impurities; Hot-pressing vitrified, non-porous, shaped glass products
- C03B32/02—Thermal crystallisation, e.g. for crystallising glass bodies into glass-ceramic articles
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/16—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay
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Definitions
- the present invention relates to the formation of internally nucleated glass ceramics articles that can be heated in the 1350-1450 0 C range for extended periods of time without significant deformation or change in shape.
- the predominant crystal phase of these glass ceramics is celsian (BaAl 2 Si 2 Os) or its strontium equivalent (SrAl 2 Si 2 Og), or solid solutions or mixtures of these compositions, all belonging to the feldspar mineral group.
- Glass-ceramic articles are produced through the controlled crystallization of glass articles.
- a glassforming batch to which a nucleating agent is commonly added, is melted and this melt cooled to a uniform glass body.
- the glass body is then subjected to a heat treatment schedule which usually comprises two phases.
- a heat treatment schedule which usually comprises two phases.
- the glass is heated somewhat above the transformation range of the glass to cause the development of nuclei therein.
- the nucleated glass is heated to a higher temperature, normally above the softening point of the glass, to cause the growth of crystals on the nuclei. Since the crystallization occurs on the innumerable nuclei developed during the nucleation step, the crystals are uniformly fine-grained and homogeneously dispersed in a glassy matrix.
- the crystals generally comprise the preponderance of the article and, therefore, endow the article with properties more similar to those of the crystal phase than those of the original glass.
- the body is crystallized in situ from a glass, it is free of voids and non-porous. Silicon semiconductors are more efficient in display or photovoltaic devices if the grains are large. Silicon melts at 1417 0 C, and it can be subsequently crystallized to the largest grains when held just below its melting point. This is because nucleation is inefficient at such high temperatures but grain growth is maximized. Since the growth of these crystallized films initially requires application of a film of molten silicon to a substrate surface, it is important that the substrate material itself be inert, able to withstand high temperature, and have a coefficient of expansion (CTE) that approximately matches that of silicon.
- CTE coefficient of expansion
- silicon If silicon is melted on an inert substrate and subsequently recrystallized near its melting point, it will remain as a coherent large-grained film upon cooling to room temperature providing the substrate approximately matches the silicon in CTE.
- the glass-ceramics of this invention can be tailored to match or be very close to the CTE of silicon.
- certain suboxide semiconductors that also display photovoltaic behavior e.g. reduced titanates and certain tantalates, require high temperatures (above 1300 0 C) to be effectively sintered. Therefore, films of these materials require a substrate which can withstand sintering temperatures above 1400 0 C.
- ceramic materials which can replace superalloy metals in certain engine components such as those used in aircraft engines and in diesel turbochargers.
- Silicon nitride is such a candidate, but it is difficult to fabricate and inherently expensive. Accordingly, there is a need for a high temperature glass ceramic material that can be utilized as an inert substrate for thin film crystal silicon production, can be tailored to match the CTE of silicon, can withstand temperatures of as high as 1450 0 C, is resistant to oxidation, and is capable of being precision formed in the fluid glassy state by pressing techniques or by simple casting into graphite or other molds.
- the present invention provides a glass-ceramic having high fracture toughness and low coefficient of thermal expansion, the glass-ceramic formed from a composition comprising, in weight percent: SiO 2 25-45%
- the glass-ceramic includes feldspar as a primary crystalline phase.
- the major phase is celsian (BaAl 2 Si 2 O 8 ) or its strontium equivalent (SrAl 2 Si 2 O 8 ) or solid solutions or mixtures of celsian (BaAl 2 Si 2 O 8 ) and its strontium equivalent
- the glass ceramic has less than 25% by volume of residual glass.
- the glass-ceramic be alkali-free and substantially free of additional fluxes.
- fluxes or additional components may be added, but typically not in excess of 5% by weight.
- the glass ceramic has a CTE from 30-55 x 10 "7 /°C in the temperature range 25-1000 0 C, has a softening temperature in excess of 1450 0 C, a fracture toughness exceeding 1.2 Kj c MPa-m' 72 , a modulus of rupture (M.O.R.) exceeding 90 MPa, and use temperature in excess of 1250 0 C, and as high as 1450 0 C, or higher.
- glass ceramics of the present invention Several uses of the glass ceramics of the present invention have been identified including high temperature refractory uses such as those required in substrates for photovoltaic devices, metallurgical casting molds, radomes and engine components.
- One embodiment comprises the steps of melting a batch of raw materials including at least one nucleating agent to a temperature of 1550 0 C to 1700 0 C for a period of time sufficient to achieve a molten homogeneous melt; forming into a desired shape, a glass article from the melt; annealing the glass article at a temperature in the range of 700 0 C to 850 0 C; heat treating the glass article at a temperature of 800 0 C to 900 0 C for a period of time sufficient for homogeneous dispersion and development of nuclei from the nucleating agent; crystallizing the glass at a temperature in the range of 950 0 C to 1450 0 C for a time sufficient to achieve maximum crystallinity thereby transforming the glass article into a glass ceramic article; and cooling the glass ceramic article.
- An internally nucleated glass ceramic that can be heated in the 1250-1450 0 C range for extended periods of time without significant deformation or shape and whose predominant crystal phase of either the feldspar celsian (BaAl 2 Si 2 O 8 ) or its strontium equivalent (SrAl 2 Si 2 O 8 ), or solid solutions or mixtures of these compositions, is disclosed.
- a glass-ceramic includes any material that is formed when a substantially glassy material is heated at elevated temperature to produce a substantially crystalline material. The heat treatment induces nucleation of one or more crystalline phases. Nucleation is accelerated by adding a component to the glass such as titania (TiO 2 ) which precipitates uniformly upon reheating the glass.
- the heat treatment is completed when the intended level of crystallinity is reached.
- These glass ceramic materials are characterized by excellent refractory characteristics and are made from glasses that can be melted to good quality at temperatures in the 1600-1675 0 C range, a range within which the effective melting of other commercial glasses or glass-ceramic parent glasses has been established.
- the glass-ceramic of the present invention may include a plurality of crystalline phases, but is comprised of a predominant primary crystalline phase of feldspar.
- the residual glass should be stiff enough so as not to cause a composite article that has been formed from the material to deform or change shape at temperatures in excess of 1250 0 C, in excess of 1300 0 C, in excess of 1350 0 C, and in excess of 1400 0 C.
- the embodiments of the glass ceramic articles of the present invention have use temperatures of greater than 125O 0 C and as high as 1450 0 C.
- the term "use temperature" indicates that an article formed from the glass ceramic will not deform when put under load or under its own weight.
- crystallinity should be at least about 70% of the weight and preferably more than 80% crystalline. Residual glass will typically be less than 25% by volume.
- Celsian is a barium feldspar, has a monoclinic structure, with crystallographic space group HIc, and its strontium equivalent has a similar monoclinic structure believed to be of the same space group. Solid solution between these end-members is believed wide but may not be complete.
- the value of these celsian-type crystals as the major phase in glass-ceramics is at least two-fold: i) the high melting point, roughly 1750 0 C for the pure barium end-member, and roughly 1710 0 C for the strontium end member, which combined with the effects of a titanate nucleating agent and residual glass present in the glass-ceramics, allows thermal stability to about
- the disclosed glass ceramics may have a CTE ranging from approximately 30-55 x 10 "7 /°C (25-1000 0 C).
- nucleating agents include: ZrO 2 ; metals such as platinum, rhodium, iridium, lead or gold; or sulphides such as ZnS.
- Other candidates include: V 2 O 5 , MoO 3 , SrF 2 , BaF 2 , WO 3 , and NiO.
- the glass-ceramic composition range of an embodiment of this invention lies in the SiO 2 -Al 2 O 3 -SrO-BaO-TiO 2 system and comprises the following area in weight percent: SiO 2 25-45, Al 2 O 3 23-37, SrO 0-30, BaO 0-35, and TiO 2 5-15.
- SrO+BaO is between 15 and 35 weight percent and the molar ratio of (SrO+BaO)/Al 2 ⁇ 3 is preferably less than 1.2, more preferably less than 1.1 and still more preferably less than 1.0.
- additional components e.g. ZrO 2 , K 2 O, ZnO, CaO, etc.
- CTE, stability, etc. certain physical characteristics
- the composition be essentially free of alkali or other oxides that can be reduced to the elemental state through reaction with silicon (e.g. PbO, ZnO, CuO, P2O5, etc.).
- silicon e.g. PbO, ZnO, CuO, P2O5, etc.
- SiO 2 -Al 2 O 3 -BaO-TiO 2 a small area of meltable glass compositions which can be heat treated to glass-ceramics displaying all the features of this invention was also found. This can be defined in weight percent as follows: SiO 2 31-41, Al 2 O 3 27-33, BaO 24-32, and TiO 2 6-12.
- the article is heat treated in order to convert it to a glass-ceramic.
- the article is placed into a gas or electric furnace and heat treated in the range of 80O 0 C to 900 0 C for a nucleation period that can range from a short as 10 minutes to as long as several hours so long as there is homogenous dispersion and development of the titanate nuclei.
- the temperature is raised to a higher temperature typically in the range of 950-1450 0 C for a crystallization period. This crystallization period should last between 4-6 hours or as long as necessary to achieve maximum crystallinity for the selected composition.
- Some siliceous residual glass remains and helps to lower the CTE of the glass- ceramic.
- the major crystal phase is feldspar of the monoclinic celsian type, either barium or strontium end-members or solid solutions or mixtures of solid solutions between these end members.
- important accessory phases are present in these glass-ceramics. These include at least one titanate phase, normally aluminum titanate (Al 2 TiOs) or rutile (TiO 2 ), and a siliceous glassy phase.
- Mullite AIoSi 2 On
- the crystals are fine-grained, typically between 0.5 and 20 urn.
- the microstructure is uniform.
- the surface of the glass-ceramic is typically grey to white, while the interior is generally grey. The whiter surface is presumed due to oxidation of small amounts of reduced titanium,
- the glass-ceramic of the present invention may be formed into any number of articles.
- the glass-ceramic is especially adapted to articles requiring low CTE, good fracture toughness, good strength, oxidation resistance, and high temperature requirements.
- fracture toughness of greater than 1.2 K ]c MPaTn" 2 is common. Fracture toughness may exceed 2, and even 2.5 Ki c MPa m' /2 .
- Modulus of rupture has been measured to be in excess of 89 ⁇ 5 M.O.R. (MPa).
- MPa M.O.R.
- the inherent oxidation-resistance of glass-ceramic permits its use where silicon nitride would oxidize. Potential uses include substrates for semiconductor crystallization.
- the high use temperature of up to 1450 0 C is necessary to melt and subsequently recrystallize silicon to its largest grain size, where efficiency for photovoltaic or other semiconductor applications can approach that of single crystals.
- the CTE match of silicon and celsian-type feldspar glass-ceramics allows formation and subsequent cooling of continuous films. This cannot be achieved with other refractory ceramic substrates like alumina, which are too high in CTE and yield tension cracks in an applied silicon film upon cooling.
- Another potential use of the barium feldspar celsian (BaAl 2 Si 2 O 8 ) and the strontium feldspar glass ceramic material of the present invention include the use for high temperature engine components. The ability to withstand temperatures of 1450 0 C is important for advanced engine components.
- the moderately low CTE of celsian-type glass-ceramics coupled with good flexural strength, toughness, and fluid precision casting capability allows these glass-ceramics to compete with expensive silicon nitride in these areas.
- Testing has indicated that the disclosed glass ceramics withstand temperatures in excess of 1400 0 C and 1450 0 C without substantial deformation or change of shape. The softening temperatures of these materials are in excess of 145O 0 C.
- a further potential application for refractory, fine-grained and non-porous celsian-type glass-ceramics are use as precision molds for the casting of high temperature metals and alloys.
- barium feldspar celsian BaAl 2 Si 2 O 8
- strontium feldspar glass ceramic material of the present invention include the use for radomes, or missile nose cones, which require high temperature use, thermal shock resistance and an absence of alkali for good microwave transparency for guidance.
- Celsian glass-ceramics are more refractory by ⁇ 150°C than currently used cordierite-based radomes.
- the barium feldspar celsian (BaAl 2 Si 2 O 8 ) and the strontium feldspar analog of celsian (SrAl 2 Si 2 O 8 ) are described in the crystallographic literature as monoclinic and belonging to the space group TlIc.
- the primary phase feldspar of the glass ceramics of the present invention are likewise believed to be monoclinic.
- compositional information is in weight percent and is, as batched, unless otherwise indicated.
- compositions were batched to yield 1 kilogram of glass using appropriate amounts of the following raw materials: BERKELEY Sand (SILICOSIL 75), low soda alumina, barium carbonate, strontium carbonate, and titanium dioxide.
- the batches were mixed for 15 minutes in a TURBULA mixer and then placed in a 650mm platinum crucible.
- the crucibles were placed in an electric (GLOBAR) furnace at 1650 0 C for 16 hours and the batch was melted to good quality molten glass.
- the melts were then poured into steel molds to yield glass patties about 4 x 8 x 3/4 inches in size. Upon cooling, the patties were moved to an annealing furnace at 775°C and held for several hours and then cooled.
- the resulting glasses were cut into slabs and heat treated according to the schedules given in Table 1. Heating rates prior to and between holds were roughly 300°C/hr. The crystal phases produced during these heat treatments were determined by x-ray diffraction. Properties were measured by standard ASTM techniques.
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- Crystallography & Structural Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
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- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Physics & Mathematics (AREA)
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- Inorganic Chemistry (AREA)
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Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010522928A JP5539204B2 (ja) | 2007-08-28 | 2008-08-27 | 耐熱性ガラスセラミック |
| EP08795614.0A EP2205533B1 (en) | 2007-08-28 | 2008-08-27 | Refractory glass ceramics |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/895,847 | 2007-08-28 | ||
| US11/895,847 US7867932B2 (en) | 2007-08-28 | 2007-08-28 | Refractory glass ceramics |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2009029263A1 true WO2009029263A1 (en) | 2009-03-05 |
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ID=39832777
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2008/010133 Ceased WO2009029263A1 (en) | 2007-08-28 | 2008-08-27 | Refractory glass ceramics |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US7867932B2 (enExample) |
| EP (1) | EP2205533B1 (enExample) |
| JP (1) | JP5539204B2 (enExample) |
| KR (1) | KR101474588B1 (enExample) |
| TW (2) | TWI408114B (enExample) |
| WO (1) | WO2009029263A1 (enExample) |
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| DE112023000360T5 (de) | 2022-01-14 | 2024-09-05 | AGC Inc. | Kristallisiertes glas, glassubstrat für eine hochfrequenzvorrichtung, flüssigkristallantenne, amorphes glas und verfahren zur herstellung eines kristallisierten glases |
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- 2008-08-27 KR KR1020107006870A patent/KR101474588B1/ko not_active Expired - Fee Related
- 2008-08-27 JP JP2010522928A patent/JP5539204B2/ja not_active Expired - Fee Related
- 2008-08-27 EP EP08795614.0A patent/EP2205533B1/en not_active Not-in-force
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN110240412A (zh) * | 2019-07-10 | 2019-09-17 | 贵州省冶金化工研究所 | 一种高温观察窗用透明氧氟硅酸盐微晶玻璃及其制备方法 |
| DE112023000360T5 (de) | 2022-01-14 | 2024-09-05 | AGC Inc. | Kristallisiertes glas, glassubstrat für eine hochfrequenzvorrichtung, flüssigkristallantenne, amorphes glas und verfahren zur herstellung eines kristallisierten glases |
| CN120081675A (zh) * | 2025-03-07 | 2025-06-03 | 北京犇犇国际新材料科技有限公司 | 一种梯度表面的辐射降温陶瓷复合材料及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2205533A1 (en) | 2010-07-14 |
| TWI408114B (zh) | 2013-09-11 |
| US20110072853A1 (en) | 2011-03-31 |
| US7867932B2 (en) | 2011-01-11 |
| KR101474588B1 (ko) | 2014-12-18 |
| JP2010537928A (ja) | 2010-12-09 |
| EP2205533B1 (en) | 2015-11-11 |
| TW201345858A (zh) | 2013-11-16 |
| JP5539204B2 (ja) | 2014-07-02 |
| TWI472496B (zh) | 2015-02-11 |
| KR20100071051A (ko) | 2010-06-28 |
| US20090056380A1 (en) | 2009-03-05 |
| TW200940470A (en) | 2009-10-01 |
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