Classifications

• • 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
  • C03C10/0018—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 monovalent metal oxide as main constituents
  • C03C10/0027—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 monovalent metal oxide as main constituents containing SiO2, Al2O3, Li2O as main constituents
• • 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
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/097—Glass compositions containing silica with 40% to 90% silica, by weight containing phosphorus, niobium or tantalum
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
  • C03B27/00—Tempering or quenching glass products
  • C03B27/012—Tempering or quenching glass products by heat treatment, e.g. for crystallisation; Heat treatment of glass products before tempering by cooling
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • 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
• • 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
  • C03C1/00—Ingredients generally applicable to manufacture of glasses, glazes, or vitreous enamels
  • C03C1/004—Refining agents
• • 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
  • C03C1/00—Ingredients generally applicable to manufacture of glasses, glazes, or vitreous enamels
  • C03C1/04—Opacifiers, e.g. fluorides or phosphates; Pigments
• • 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
  • C03C10/0054—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 PbO, SnO2, B2O3
• • 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
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/083—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
• • 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
  • C03C3/00—Glass compositions
  • C03C3/04—Glass compositions containing silica
  • C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
  • C03C3/083—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound
  • C03C3/085—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal
  • C03C3/087—Glass compositions containing silica with 40% to 90% silica, by weight containing aluminium oxide or an iron compound containing an oxide of a divalent metal containing calcium oxide, e.g. common sheet or container glass
• • 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
  • C03C4/00—Compositions for glass with special properties
  • C03C4/02—Compositions for glass with special properties for coloured glass
• • 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
  • C03C2204/00—Glasses, glazes or enamels with special properties

Definitions

• the context of the present application is that of transparent low expansion glass-ceramics of lithium aluminosilicate (LAS) type containing a solid solution of b-quartz as the main crystalline phase.
• LAS lithium aluminosilicate
• transparent glass-ceramics of lithium aluminosilicate (LAS) type containing a solid solution of b-quartz as the main crystalline phase and having a low lithium content; said glass-ceramics being materials that are entirely suited to making cooktops associated with induction heating;
• LAS lithium aluminosilicate
• lithium aluminosilicate glasses precursors of these glass-ceramics
• Transparent glass-ceramics - of the lithium aluminosilicate (LAS) type, containing a solid solution of b-quartz as the main crystalline phase - have been in existence for more than 20 years. They are described in numerous patent documents and in particular in patent US 5 070 045 and patent application WO 2012/156444. They are used more particularly as the material for constituting cooktops, cooking utensils, microwave oven bottoms, fireplace windows, fireplace inserts, stove windows, oven doors (in particular for pyrolytic and catalytic ovens), and fire-windows.
• LAS lithium aluminosilicate
• CTE linear coefficient of thermal expansion
• plates used with radiant heating can be raised to temperatures as high as 725°C, and in order to be able to withstand the thermal shocks and the temperature gradients that occur within them, their CTE is low, generally lying in the range ⁇ 10xl0 7 per kelvin (1C 1 ), preferably in the range ⁇ 3x10 " 7 K _1 from 25°C to 700°C; and
• the plates proposed in the present application are suitable for use with conventional induction heating; they withstand temperatures of 400°C, and exceptionally thermal shocks at 450°C.
• opacifier may be deposited on the bottom face of such a plate or the material from which it is constituted may be strongly colored. If this case, some minimum level of transmission must nevertheless be conserved so that displays can be seen, as a result of light emitted by light- emitting diodes (LEDs) placed under the plate.
• LEDs light- emitting diodes
• Lithium is one of the main components of these glass-ceramics (of the lithium aluminosilicate (LAS) type, which are transparent and contain a solid solution of b-quartz as the main crystalline phase).
• lithium is present in the composition of said glass-ceramics, generally at contents lying in the range 2.5% to 4.5% (see for example the teaching of patents US 9 051 209 and US 9 051 210), more generally at contents of 3.6% to 4.0%, by weight (expressed in terms of Li 2 0). It is used essentially as an component of the solid solution of b-quartz. It makes it possible within the glass-ceramics to obtain CTE values that are low or even zero. It constitutes a particularly high performance melting agent for the precursor glass (its impact being observed most particularly on high temperature viscosity). At present, the supply of lithium is less reliable than it used to be. In any event, this element is becoming more expensive. The reason for this recent pressure on the availability and the price of lithium lies in the increasing demand for lithium for producing lithium batteries.
• patent US 9 446 982 describes colored transparent glass-ceramics of lithium aluminosilicate (LAS) type containing a solid solution of b-quartz as the main crystalline phase and containing lithium contents (expressed in terms of U 2 0) that are in the range 2% to less than 3% by weight (at least 2% by weight, with reference to controlling crystallization), and magnesium contents (expressed in terms of MgO) lying in the range 1.56% to 3% by weight, with reference to the looked-for CTE value.
• LAS lithium aluminosilicate
• CTE values in the range lOxlO ⁇ K 1 to 25x lO 7 IC 1 , between ambient temperature and 700°C, are aimed, with reference to the technical problem of the compatibility of said glass-ceramics with their decoration;
• patent application US 2015/0197444 describes transparent glass- ceramics of the lithium aluminosilicate (LAS) type containing a solid solution of b-quartz as the main crystalline phase and presenting a controlled transmission curve.
• the compositions described are free from As 2 C>3 and Sb 2 C>3 and they contain tin oxide (Sn0 2 ) as fining agent. They generally contain 2.5% to 4.5% by weight of U 2 0.
• the example compositions contain high contents of U 2 0, lying in the range 3.55% to 3.80% by weight;
• patent US 9 018 113 describes colored transparent glass-ceramics presenting transmission curves that are optimized in the visible and infrared ranges and that are suitable for use as cooktops associated with induction heating.
• Their composition contains 1.5 wt.% to 4.2 wt.% U 2 0; specifically the example compositions all contain contents of Li 2 0 superior to 2.9 wt.%; and
• patent application DE 10 2018 110 855 describes transparent glass- ceramics having a CTE of ⁇ 10x l0 ‘7 K '1 (from 20°C to 700°C), of composition containing 3.0 wt.% to 3.6 wt.% U 2 0 (preferably in the range 3.2 wt.% to 3.6 wt.% of U 2 0), and V 2 0 5 or Mo0 3 as coloring agents.
• the inventors have found it appropriate to seek glass-ceramic compositions of low lithium content (maximum content 2.9% by weight of U 2 0); the glass-ceramics in question, transparent, of lithium aluminosilicate (LAS) type and containing a solid solution of b-quartz as the main crystalline phase, being entirely suitable as material for making cooktops usable with induction heating (conventional induction heating; said cooktops being subjected to temperatures that reach 450°C only exceptionally, and generally no more than 400°C). It was also most desirable:
• the precursor glasses of said glass-ceramics to present properties similar to those of precursor glasses for presently fabricated glass-ceramics so that the industrial process can be transposed easily;
• said precursor glasses • for said precursor glasses to be capable of being colored and most particularly of developing a black color while they are being cerammed, without a level of haze appearing that impedes good visibility of the red light emitted by light-emitting diodes (LEDs) arranged under cooktops.
• LEDs light-emitting diodes
• said CrE( 25- 4 5 o°c) is less than or equal to Mx lO ⁇ IC 1 , advantageously less than or equal to lOx lO ⁇ K '1 ) and also, opportunely, a CTE lying in the range ⁇ 14x l0 7 K '1 between 25 and 700°C (-14X 10 '7 K _1 £ CTE (25 -7OO°C) £ +14X 10 ‘7 K ‘1 ), - ⁇ thus to be transparent (even if they are usually strongly colored): at the intended utilization thickness (cooktops typically have a thickness of 1 millimeter (mm) to 8 mm, more generally lying in the range 2 mm to 5 mm and often having a thickness of 4 mm), said glass-ceramics need to present integrated transmission, TL or Y (%) greater than or equal to 1% and a diffusion percentage (diffusion or haze (%)) less than 2%.
• these measurements may be performed using a spectrometer having an integrating sphere.
• the integrated transmission (TL or Y (%)) in the visible range (from 380 nanometers (nm) to 780 nm) and the diffusion percentage (diffusion or haze (%)) are calculated using the standard ASTM D 1003-13 (under D65 illuminant with 2° observer); and
• said precursor glass must present a low liquidus temperature ( ⁇ 1400°C) and a high viscosity at the liquidus (> 400 pascal seconds (Pa.s), preferably > 700 Pa.s), thereby facilitating forming; and/or, advantageously and
• said precursor glass must possess a low viscosity at high temperature (T 3 op a.s £ 1640°C, advantageously ⁇ 1630°C), thereby facilitating fining.
• said precursor glass is also highly appropriate for said precursor glass to be capable of being transformed into glass-ceramic in a short length of time ( ⁇ 3 hours (hr)), preferably in a very short length of time ( ⁇ 1 hr), and/or, advantageously and, for said precursor glass to present electrical resistivity at a viscosity of 30 Pa.s that is less than 50 ohm-centimeters (W.ah) (and preferably less than 20 W.ah).
• W.ah ohm-centimeters
• glass-ceramics of lithium aluminosilicate (LAS) type, containing a solid solution of b-quartz as the main crystalline phase
• LAS lithium aluminosilicate
• Said glass-ceramics constitute the first aspect of the present application.
• these glass-ceramics present the following composition, expressed in percentages by weight of oxides:
• S1O2 (63%-67.5%): the content of S1O2 (363%) must be suitable for obtaining a precursor glass (for the glass-ceramic) that is sufficiently viscous to guarantee a minimum value of the liquidus viscosity.
• the content of S1O2 is limited to 67.5%, insofar as the greater the content of S1O2, the greater the high-temperature viscosity of the glass, and thus the glass is more difficult to melt. Comparative example A illustrates this limitation. In preferred manner, the Si0 2 content lies in the range 65% to 67% (bounds included).
• P2O5 (0-5%): this compound is optionally present. To be effective, when present, it is generally present at at least 0.5%. As a substitute for Si02, P2O5 serves to reduce the liquidus temperature, in particular when the ZnO content is large (i.e. >2.5%). This point is illustrated by comparing Example 4 (with 2.11% P 2 0 5 ) and Example 11 (no P 2 0 5 (0.05%)). In advantageous manner, to obtain a significant effect on the liquidus temperature, P2O5, present, is present at a content lying in the range 1% to 5% (bounds included). In a very advantageous manner, P2O5, present, is present at a content lying in the range 1% to 3% (bounds included).
• the minimum content is advantageously 2.2%.
• a U 2 0 content in the range 2.2% to 2.85% (bounds included) is preferred;
• a Li 2 0 content in the range 2.2% to 2.80% (bounds included) is most particularly preferred.
• MgO (0-1.5%) this compound is optionally present. In order to be effective, when present, it is generally present at at least 0.1%. This compound decreases high-temperature viscosity of the precursor glass. It forms part of the solid solution of b-quartz. It has less impact on devitrification than ZnO (see below) but it greatly increases the CTE of the glass-ceramic (as shown in comparative example C). That is why its content, when present, is limited to 1.5%. When present, it is advantageously present in the range 0.1% to 1.4%, in particular in the range 0.1% to 1.37%, more particularly in the range 0.1% to 1.35%, still more particularly in the range 0.1% to 1.3%. In any event the following condition needs to be satisfied: (0.74 MgO + 0.19 BaO + 0.29 SrO + 0.53 CaO + 0.48 Na 2 0 + 0.32 K 2 0) / U 2 0 ⁇ 0.9.
• this compound also serves to diminish the high- temperature viscosity of the precursor glass and it also forms part of the solid solution of b-quartz. Compared with U 2 0, it increases the CTE of the glass- ceramic, but does so in moderate manner, which makes it possible to obtain glass-ceramics having CTEs less than HxlO ⁇ K 1 between 25 and 450°C. When present in too great a quantity, it leads to unacceptable devitrification (as illustrated in comparative example D). Advantageously, it is present in the range 1% to 3%. In the absence of P 2 0 5 , its content lies preferably in the range 1% to 2.5% (see above).
• Zr0 2 is advantageously present (but not necessarily). With reference to effectiveness, it should generally be present at at least 0.1%. These compounds, Ti0 2 and Zr0 2 enable the precursor glass to nucleate and enable a transparent glass-ceramic to be formed. The combined presence of these two compounds enables nucleation to be optimized. Too great a content of Ti0 2 makes it difficult to obtain a glass-ceramics that is transparent. Ti0 2 is advantageously present at a content lying in the range 2% to 4% (bounds included), and very advantageously it is present at a content lying in the range 2% to 3% (bounds included). Too great a content of Zr0 2 leads to unacceptable devitification. Zr0 2 is advantageously present at a content lying in the range 0 to 1.5% (bounds included), very advantageously it is present at a content lying in the range 1% to 1.5% (bounds included).
• SrO is generally not present in the form of added raw material. In such a context (no SrO present as added raw material), if SrO is present, it is present only as inevitable traces ( ⁇ 100 ppm), brought in as impurity with at least one of the raw materials used or within the cullet of glass and/or glass-ceramic used.
• Fining agent(s) the composition of the glass-ceramics of the present application advantageously includes at least one fining agent such as AS 2 03, Sb 2 0 3 , Sn0 2 , Ce0 2 , a chloride, a fluoride, or a mixture thereof.
• Said at least one fining agent is present in an effective quantity (for performing chemical fining), which conventionally does not exceed 2% by weight. It is thus generally present in the range 0.05% to 2% by weight.
• fining is performed by using Sn0 2 , generally with 0.05% to 0.6% by weight of Sn0 2 , and more particularly with 0.15% to 0.4% by weight of Sn0 2 .
• the compositions of the glass-ceramics of the present application contain neither As 2 0 3 nor Sb 2 0 3 , or they contain only inevitable traces of at least one of these toxic compounds (As 2 0 3 + Sb 2 0 3 ⁇ 1000 ppm).
• traces of at least one of these compounds are present, they are present as contamination; by way of example, this may be due to the presence of recycled materials of the cullet type (derived from old glasses or glass-ceramics refined with these compounds) in the charge of vitrifiable raw materials.
• the presence of at least one other fining agent, such as Ce0 2 , a chloride, and/or a fluoride is not excluded, but Sn0 2 is preferably used as the only fining agent.
• Coloring agent(s) the composition of the glass-ceramics advantageously includes at least one coloring agent.
• Said at least one coloring agent is present in an effective quantity (generally at least 0.01% by weight); it is conventionally present at at most 2% by weight, or indeed at most 1% by weight.
• Said at least one coloring agent is conventionally selected from oxides of transition elements (V 2 Os, CoO, Cr 2 0 3 , Fe 2 0 3 (see below), NiO, ...) and of rare earths (Nd 2 03, Er 2 0 3 , ).
• vanadium oxide V 2 Os is used since said vanadium oxide leads to a low absorption (in particular in infra-red range) of the precursor glass, which is advantageous for melting. The absorption it makes possible is generated during the ceramming treatment (during which it is partially reduced). It is particularly advantageous to combine V 2 Os with other coloring agents such as Cr 2 C>3, CoO, or Fe 2 0 3 (see below), since that enables transmission to be modulated. With reference to the requirements set out below (formulated for the utilization thickness, typically in the range 1 mm to 8 mm, more generally in the range 2 mm to 5 mm, and often 4 mm):
• TL integrated transmission
• coloring agents Fe 2 0 3 has a special place. It has an effect on color and it is indeed often present, at a greater or lesser quantity as an impurity (e.g. coming from the raw material). Nevertheless, it may also be added in order to adjust color. Its authorized presence "in large quantity" in the composition of glass-ceramics of the present application makes it possible to use raw materials that are less pure and thus often less expensive.
• ingredients involved, or potentially involved, in the composition of glass-ceramics of the present application can indeed represent 100% by weight of the composition of glass-ceramics of the present application, but, a priori, the presence of at least one other compound is not to be totally excluded, providing it is in a low quantity (generally less than or equal to 3% by weight) and does not substantially affect the properties of the glass-ceramics.
• the following compounds may be present, at a total content of less than or equal to 3% by weight, each of them being present at a content less than or equal to 2% by weight: B 2 0 3 , Nb 2 0 5 , Ta 2 0 5 , W0 3 , and Mo0 3 .
• B 2 0 3 it is thus potentially present (0-2%).
• B 2 0 3 it is generally present at at least 0.5%. It is more generally present in the range 0.5% to 1.5%.
• B 2 0 3 is rarely present in practice as an added raw material, it being generally present only in the state of traces (at contents of less than 0.1 %).
• B 2 0 3 favors ceramming into b-spodumene and the apparition of diffusion (or haze).
• the compositions of glass-ceramics of the present application are advantageously exempt from B 2 0 3 , with the exception of inevitable traces.
• ingredients involved, or potentially involved, in the composition of glass-ceramics of the present application (Si0 2 , P 2 Os, Al 2 0 3 , Li 2 0, MgO, ZnO, Ti0 2 , Zr0 2 , BaO, SrO, CaO, Na 2 0, K 2 0, fining agent(s), and coloring agent(s)), thus represent at least 97% by weight, or indeed 98% by weight, or at least 99% by weight, or even 100% by weight (see above) of the composition of glass-ceramics of the present application.
• the glass-ceramics of the present application thus contain Si0 2 , Al 2 0 3 , U 2 0, ZnO, and MgO as essential components for the solid solution of b-quartz (see below).
• This solid solution of b-quartz represents the main crystalline phase.
• This solid solution of b-quartz generally represents more than 80% by weight of the total crystallized fraction. It generally represents more than 90% by weight of said total crystallized fraction.
• the size of the crystals is small (typically less than 70 nm), which enables the glass-ceramics to be transparent (integrated transmission > 1% and diffusion ⁇ 2%).
• the glass-ceramics of the present application contain about 10% to about 40% by weight of residual glass.
• the glass-ceramics of the present application thus have a coefficient of thermal expansion lying in the range ⁇ 14x l0 7 K 1 , advantageously in the range ⁇ IOcIO ⁇ K 1 , between 25 and 450°C; and, also advantageously, a coefficient of thermal expansion lying in the range ⁇ HxlO 7 ⁇ 1 between 25 and 700°C (see above).
• the present application provides articles that are constituted at least in part of a glass-ceramic of the present application as described above.
• Said articles are optionally constituted in full of a glass- ceramic of the present application.
• Said articles advantageously consist in cooktops, which are a priori bulk colored (see above). Nevertheless, that is not the only application for which they can be used. In particular, they may constitute the material constituting cooking utensils, microwave oven bottoms, oven doors, whether colored or not.
• the glass-ceramics of the present application are logically used in contexts that are compatible with their CTEs.
• cooktops according to the invention are strongly (adapted and) recommended for use with conventional induction heating elements.
• the present application provides aluminosilicate glasses that are precursors for the glass-ceramics of the present application, as described above.
• said glasses present a composition that makes it possible to obtain said glass-ceramics.
• Said glasses generally present a composition corresponding to that of said glass-ceramics, but the correspondence is not necessarily complete insofar as the person skilled in the art readily understands that the thermal treatments applied to such glasses for obtaining glass-ceramics are likely to have some effect on the composition of the material.
• the glasses of the present application are obtained in conventional manner by melting a vitrifiable charge of raw materials (raw materials making them up being present in the appropriate proportions). Nevertheless, it can be understood (and will not surprise the person skilled in the art) that the charge in question may contain glass and/or glass-ceramic cullet. Said glasses are particularly advantageous in that:
• Said glasses present advantageous devitrification properties, in particular compatible with using forming methods involving rolling, floating, and pressing.
• Said glasses present a low liquidus temperature ( ⁇ 1400°C) and high viscosity at the liquidus (>400 Pa.s, preferably >700 Pa.s); and/or, and advantageously and
• liquidus temperature is low, that viscosity at the liquidus is high, and that viscosity at high temperature is low (see below).
• the present application provides a method of preparing an article constituted at least in part by a glass-ceramic of the present application, as described above.
• Said method is a method by analogy.
• said method comprises heat treatment of a charge of vitrifiable raw materials (it being understood that such a vitrifiable charge may contain glass and/or glass-ceramic cullet (see above)) under conditions that ensure melting and fining in succession, followed by shaping the fined molten precursor glass (said shaping possibly being performed by rolling, by pressing, or by floating), followed by ceramming (or crystallization) thermal treatment of the shaped refined molten precursor glass.
• Table I specifies raw materials usually used in the charges of vitrifiable raw materials to have each one of the desired oxides present in the composition of precursor glasses and corresponding glass-ceramics. This list is in no way exhaustive. Table I
• Each one of the used raw material is able to bring impurities which are taken into account in the calculation of quantities of different raw materials constituting the verifiable mixture (charge).
• spodumene contains, depending on its source, variable contents in U 2 0, Si0 2 and Al 2 0 3 as well impurities such as Na 2 0, K 2 0, Fe 2 0 3 and P 2 0 5 .
• Li 2 0 is usually brought with at least one of the following raw materials: spodumene, petalite, lithium carbonate, lithium feldspar or a mixture thereof. In a preferred manner, Li 2 0 is only brought by spodumene (this is the case for the following examples and comparative examples (see tables III and IV)).
• the ceramming thermal treatment generally comprises two steps: a nucleation step and another step of growing the crystals of the b-quartz solid solution.
• Nucleation generally takes place in the temperature range 650°C to 830°C and crystal growth in the temperature range 850°C to 950°C.
• Concerning the duration of each of these steps mention may be made in entirely non-limiting manner of about 5 minutes (min) to 60 min for nucleation and about 5 min to 30 min for crystal growth. The person skilled in the art knows how to optimize, more particularly with reference to the desired transparency, the temperatures and the durations of these two steps as a function of the composition of the precursor glasses.
• Said method of preparing an article, constituted at least in part of a glass-ceramic of the present application thus comprises in succession:
• the two successive steps of obtaining a shaped refined glass (precursor of the glass-ceramic) and ceramming said shaped refined glass may be performed immediately one after the other, or they may be spaced apart in time (on a single site or on different sites).
• the charge of vitrifiable raw materials has a composition that makes it possible to obtain a glass-ceramic of the present application, thus presenting the composition by weight as specified above (advantageously including Sn02 as a fining agent, (in the absence of AS2O3 and Sb 2 0 3 (see above)), very advantageously Sn0 2 as single fining agent (generally 0.05% to 0.6% by weight of Sn02, and more particularly 0.15% to 0.4% by weight of Sn0 2 )).
• the ceramming performed on the glass obtained from such a charge is entirely conventional. It is mentioned above that said ceramming may be obtained in a short length of time ( ⁇ 3 hr), or indeed in a very short length of time ( ⁇ 1 hr).
• the precursor glass In the context of preparing an article, such as a cooktop, when the precursor glass has been obtained by rolling or floating, it is generally cut before the ceramming treatment (ceramming cycle). It is generally also formed and decorated. Such forming and decorating steps may be performed before or after the ceramming thermal treatment. By way of example, the decorating may be performed by screen-printing.
• ceramming cycle ceramming cycle
• the decorating may be performed by screen-printing.
• the crucibles containing said mixtures were then placed in a furnace preheated to 1550°C.
• the furnace was heated with MoSi electrodes.
• the crucibles were subjected therein to a melting cycle of the following type:
• the crucibles were then extracted from the furnace and the molten glass was poured onto a preheated steel plate. It was rolled to have a thickness of 6 mm. Glass plates were thus obtained. They were annealed at 650°C for 1 hr and subsequently cooled down slowly.
• Viscosities were measured using a rotational viscometer (Gero).
• T 30 Pa.s (°C) corresponds to the temperature at which the viscosity of the glass was 30 Pa.s.
• Tug (°C) is the liquidus temperature.
• the liquidus temperature is given by a range of temperatures and associated viscosities: the highest temperature corresponds to the minimum temperature at which no crystal was observed, the lowest temperature corresponds to the maximum temperature at which crystals were observed.
• the experiments were carried out on precursor glass volumes of about 0.5 cubic centimeters (cm 3 ) that were held for 17 h at the temperature of the test and the observations were performed by optical microscopy. The phase of the observed crystals is given in the tables below.
• the resistivity of glass was measured while measuring viscosity.
• the table gives the resistivity measured at the temperature for which the viscosity was 30 Pa.s.
• glass-ceramics contain a solid solution of b-quartz as the main crystalline phase (as verified by X-ray diffraction).
• DIL 420C high-temperature dilatometer
• Examples 1 to 4 are preferred because of the particularly advantageous properties of the precursor glass: see the values given for high- temperature viscosity (T30p a.s ⁇ 1630°C) and for liquidus viscosity (> 700 Pa.s).
• Examples 4 and 11 show the advantage of having P 2 0 5 present in the composition of the precursor glass. This presence leads to a reduction in the liquidus temperature (about -15°C) and consequently to an increase in viscosity at the liquidus temperature (+ 200 Pa.s).
• the precursor glasses of Examples 5 to 15 present preferred values for viscosity at high temperature ( ⁇ 1630°C).
• the precursor glasses of Examples 16 to 20 present preferred values for viscosity at the liquidus (> 700 Pa.s).
• Examples 24 to 26 show the use of SrO in complement to BaO.
• Examples A to E are comparative examples.
• the content of Si0 2 is high (67.88%).
• the high-temperature viscosity is too high. It would be particularly difficult to manage melting and fining said precursor glass.
• the content of MgO is too high (1.74%) and the ratio (0.74 MgO + 0.19 BaO + 0.29 SrO + 0.53 CaO + 0.48 Na 2 0 + 0.32 K 2 0) / U 2 0 is greater than 0.90. Consequently the CTE of the glass-ceramic is too high. Said glass-ceramic is therefore not suitable to be the material for making cooktops that are to be used with (conventional) induction heating elements.

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