Lithium silicate-low quartz glass ceramic

LITHIUM SILICATE-LOW QUARTZ GLASS CERAMIC

The invention relates to lithium silicate-low quartz-glass ceramic which is suitable in particular for use in dentistry, preferably for the preparation of dental restorations, as well as to precursors for the preparation of this glass ceramic.

Lithium silicate glass ceramics are characterized as a rule by very good mechanical properties, which is why they have been used for some time in the dental field, and there primarily for the preparation of dental crowns and small dental bridges.

US 5,507,981 and US 5,702,514 describe lithium disilicate glass ceramics which are processed to form dental restorations by pressing in the viscous state. However, the use of a deformable crucible is essential, which makes the processing very expensive.

EP 827 941 and EP 916 625 disclose lithium disilicate glass ceramics which can be given the shape of the desired dental restoration by pressing or machining.

EP 1 505 041 and EP 1 688 398 describe processes for the preparation of dental restorations from lithium disilicate glass ceramics. As an intermediate product a glass ceramic with lithium metasilicate as main crystal phase, which can be very easily machined e.g. by means of CAD/CAM processes, is produced first. This intermediate product is then subjected to a further heat treatment in order to form the desired highstrength lithium disilicate glass ceramic. The heat treatments used during the process are to be chosen such that the formation of undesired crystal phases, such as for example cristobalite, is prevented.

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- 2 WO 2013/053864 discloses lithium silicate glass ceramics which contain divalent metal oxide and can be processed to form dental restorations by hot pressing as well as by machining.

Glass ceramics are known from WO 2013/164256 which have lithium disilicate as main crystal phase and apatite as a further crystal phase. The glass ceramics are characterized by high chemical stability and can be shaped to form the desired dental restorations by machining or hot pressing.

□S 2015/0104655 describes glass ceramics which, depending on the composition and the temperature treatment chosen for the crystallization, can contain lithium disilicate, lithium metasilicate, lithium phosphate, cristobalite, tridymite, quartz or spodumene as crystal phases. The glass ceramics are intended in particular to veneer zirconium oxide ceramics.

However, the machining of the conventional lithium disilicate glass ceramics is possible only with difficulty because of their high strength and it therefore as a rule involves a high wear of the tools used. The likewise possible machining of corresponding lithium metasilicate glass ceramics as precursors is much easier. However, this requires yet a further heat treatment to produce the restoration from highstrength lithium disilicate glass ceramic after the shaping by machining.

There is therefore a need for lithium silicate glass ceramics which are easily machinable and do not require a further heat treatment after this processing in order to give the produced dental restoration the desired mechanical properties. The lithium silicate glass ceramics are to have not only very good mechanical properties, but likewise also very good optical properties, in order that they also fulfil the high aesthetic demands which are made on a restorative dental material.

- 3 The lithium silicate-low quartz glass ceramic according to the invention is characterized in that it comprises lithium silicate as main crystal phase and low quartz as further crystal phase.

It has surprisingly been shown that the glass ceramic according to the invention unites a combination of very desirable mechanical and optical properties, such as are necessary precisely for a restorative dental material. The glass ceramic has a high strength and nevertheless it can be given the shape of a dental restoration easily by machining. There is no need for a subsequent heat treatment to achieve a satisfactory strength. It was furthermore not to be expected that very good optical properties can nevertheless be achieved by the provision of low quartz as further crystal phase in addition to lithium silicate as main crystal phase. This is because many additional crystal phases have a negative effect on the optical properties of lithium silicate glass ceramics. For example they can decrease the translucence and they can likewise impair the ability of the glass ceramic to be dyed, which can lead to substantial difficulties in the imitation of the colour of the natural tooth material to be replaced.

The lithium silicate-low quartz glass ceramic according to the invention in particular comprises 59.0 to 79.0, preferably 64.0 to 78.0 and particularly preferably 64.0 to 76.0 wt.-% S1O2.

In another embodiment, the lithium silicate-low quartz glass ceramic according to the invention in particular comprises 68.0 to 79.0, preferably 69.0 to 78.0 and particularly preferably 70.0 to 76.0 wt.-% SiO?.

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- 4 It is further preferred that the lithium silicate-low quartz glass ceramic according to the invention comprises 8.0 to 15.0, particularly preferably 9.0 to 14.0 and quite particularly preferably 10.0 to 13.5 wt.-% L12O. It is assumed that L12O lowers the viscosity of the glass matrix and thus promotes the crystallization of the desired phases.

In a further preferred embodiment, the glass ceramic comprises 0 to 9.0, preferably 2.0 to 6.0 and particularly preferably 3.0 to 5.0 wt.-% P2O5. It is assumed that the P2O5 acts as nucleating agent.

It is also preferred that the glass ceramic comprises 1.0 to 8.0 and in particular 2.0 to 7.0 wt.-% oxide of monovalent elements Me^IzO selected from the group of K2O, ΝθςΟ, Rb2Û, CS2O and mixtures thereof.

The glass ceramic particularly preferably comprises at least one and in particular all of the following oxides of monovalent elements Me^O in the amounts specified:

<td> Component</td><td> wt.-%</td>

<td> K₂O</td><td> 0 to 5.0</td>

<td> Na₂O</td><td> 0 to 2.0</td>

<td> Rb₂O</td><td> 0 to 8.0</td>

<td> CS2O</td><td> 0 to 7.0.</td>

In a particularly preferred embodiment, the glass ceramic according to the invention comprises 0 to 5.0, preferably 1.0 to 4.0 and particularly preferably 2.0 to 3.5 wt.-% K2O.

Furthermore, it is preferred that the glass ceramic comprises 1.0 to 9.0, preferably 2.0 to 8.0 and particularly preferably 3.0 to 7.0 wt.-% oxide of divalent elements Me^ITO selected from the group of CaO, MgO, Srô, Znô and mixtures thereof.

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- 5 In a further preferred embodiment, the glass ceramic comprises less than 2.0 wt.-% BaO. The glass ceramic is in particular substantially free from BaO.

The glass ceramic preferably comprises at least one and in particular all of the following oxides of divalent elements Me^ITO in the amounts specified:

<td> Component</td><td> wt.-%</td>

<td> CaO</td><td> 0 to 3.0</td>

<td> MgO</td><td> 0 to 6.0</td>

<td> SrO</td><td> 0 to 4.0</td>

<td> ZnO</td><td> 0 to 9.0</td>

In a particularly preferred embodiment, the glass ceramic according to the invention comprises 1.0 to 6.0, in particular 1.5 to 6.0, preferably 2.0 to 5.5, particularly preferably 3.1 to 5.5 and quite particularly preferably 3.4 to 5.0 wt.-% MgO.

A glass ceramic is further preferred which comprises 0 to 8.0, preferably 1.0 to 7.0 and particularly preferably 2.0 to 6.5 wt.-% oxide of trivalent elements Μβ^ΙΙΣ2θ3 selected from the group of AI2O3, B2O3, Y2O3, La2Û3, Ga2Û3, In?O3 and mixtures thereof.

The glass ceramic particularly preferably comprises at least one and in particular all of the following oxides of trivalent elements Me^m2O3 in the amounts specified:

Component

AI2O3

B2O3

Y2O3 wt. -¾

1.0 to 6.0 to 4.0 to 5.0

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<td> La₂O3</td><td> 0 to 5.0</td>

<td> Ga₂O3</td><td> 0 to 3.0</td>

<td> In₂0s</td><td> C to 5.0</td>

In a particularly preferred embodiment, the glass ceramic according to the invention comprises 1.0 to 6.0 and preferably 2.0 to 5.0 wt.-% AI2O3.

Furthermore, a glass ceramic is preferred which comprises 0 to 10.0 and particularly preferably 0 to 8.0 wt.-% oxide of tetravalent elements Me^IV0₂ selected from the group of ZrO₂, TiÛ2, SnO₂, Ce02, GeO₂ and mixtures thereof.

The glass ceramic particularly preferably comprises at least one and in particular all of the following oxides of tetravalent elements Me^IVO2 in the amounts specified:

Component wt.-%

ZrO₂ to 3.0

TiO₂ 0 to4.0

SnÛ2 0 to3.0

GeOz 0 to 9.0, in particular 0 to 8.0

CeO₂ C to4.0.

In a further embodiment, the glass ceramic comprises 0 to 8.0, preferably 0 to 6.0 wt.-% oxide of pentavalent elements Me^v₂Os selected from the group of V2O5, Ta₂O5, Nb₂Os and mixtures thereof.

The glass ceramic particularly preferably comprises at least one and in particular all of the following oxides of pentavalent elements Me^v₂Os in the amounts specified:

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<td></td><td> - 7 -</td>

<td> Component</td><td> wt</td>

<td> V2O5</td><td> 0 to 2.0</td>

<td> Ta2Os</td><td> 0 to 5.0</td>

<td> Nb₂Os</td><td> 0 to 5.0</td>

In a further embodiment, the glass ceramic comprises 0 to 5.0, preferably 0 to 4.0 wt.-% oxide of hexavalent elements Me^VIOa selected from the group of WO3, M0O3 and mixtures thereof.

The glass ceramic particularly preferably comprises at least one and in particular all of the following oxides Me^VIOs in the amounts specified:

Component wt.-%

WO3 0 to 3.0

M0O3 0 to 3.0

In a further embodiment, the glass ceramic according to the invention comprises 0 to 1.0 and in particular 0 to 0.5 wt.-% fluorine.

A glass ceramic is particularly preferred which comprises at least one and preferably all of the following components in the amounts specified:

Component

S1O2

Li₂O

P2O5

Me^T2O

MeⁿO

Me^TII2O₃ wt

59.0 to 79.0 or 68.0 to 79.0

8.0 to 15.0 to 9.0

1.0 to 8.0

1.0 to 9.0 to 8.0

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<td> Me^IV0₂</td><td> 0</td><td> to 10.0</td>

<td> Me^v2©5</td><td> 0</td><td> to 8.0</td>

<td> Me^VI0₃</td><td> 0</td><td> to 5.0</td>

<td> fluorine</td><td> 0</td><td> to 1.0,</td>

wherein Me^O, Me^IX0, Meⁿⁱ2Û3, Me^IVÛ2, Me^v2Ûs and Me^VIÛ3 have the above-specified meaning.

In a further particularly preferred embodiment, the glass ceramic comprises at least one and preferably all of the following components in the amounts specified:

<td colspan="2"> Component</td><td colspan="2"> wt.-%</td>

<td></td><td> SiO₂</td><td colspan="2"> 59.0 to 79.0 or 68.0 to 79.0</td>

<td> 15</td><td> Li₂0</td><td> 8.</td><td> 0 to 15.0</td>

<td></td><td> P2O5</td><td> 0</td><td> to 9.0</td>

<td></td><td> K₂O</td><td> 0</td><td> to 5.0</td>

<td></td><td> Na₂O</td><td> 0</td><td> to 2.0</td>

<td></td><td> Rb₂O</td><td> 0</td><td> to 8.0</td>

<td> 20</td><td> CS2O</td><td> 0</td><td> to 7.0</td>

<td></td><td> CaO</td><td> 0</td><td> to 3.0</td>

<td></td><td> MgO</td><td> 0</td><td> to 6.0</td>

<td></td><td> SrO</td><td> 0</td><td> to 4.0</td>

<td></td><td> ZnO</td><td> 0</td><td> to 9.0</td>

<td> 25</td><td> AI2O3</td><td> 1.</td><td> 0 to 6.0</td>

<td></td><td> B2O3</td><td> C</td><td> to 4.0</td>

<td></td><td> Y2O3</td><td> 0</td><td> to 5.0</td>

<td></td><td> La2Û3</td><td> 0</td><td> to 5.0</td>

<td></td><td> Ga2©3</td><td> 0</td><td> to 3.0</td>

<td> 30</td><td> In₂O3</td><td> 0</td><td> to 5.0</td>

<td></td><td> ZrO2</td><td> C</td><td> to 3.0</td>

<td></td><td> TiO₂</td><td> 0</td><td> to 4.0</td>

<td></td><td> SnO2</td><td> 0</td><td> to 3.0</td>

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<td colspan="4"> GeO2 0 to 9.0, in particular 0 to 8.0</td>

<td> CeO2</td><td> 0</td><td> to</td><td> 4.0</td>

<td> V2O5</td><td> 0</td><td> to</td><td> 2.0</td>

<td> Ta2Ûs</td><td> 0</td><td> to</td><td> 5.0</td>

<td> Nb₂O₅</td><td> 0</td><td> to</td><td> 5.0</td>

<td> WO3</td><td> 0</td><td> to</td><td> 3.0</td>

<td> M0O3</td><td> 0</td><td> to</td><td> 3.0</td>

<td> fluorine</td><td> 0</td><td> to</td><td> 1.0.</td>

Some of the above-named components can serve as colorants and/or fluorescent agents. The glass ceramic according to the invention can also comprise still further colorants and/or fluorescent agents. These can e.g. be selected from BÏ2Û3 or B12O5 and in particular from further inorganic pigments and/or oxides of d-block and f-block elements, such as the oxides of Mn, Fe, Co, Pr, Nd, Tb, Er, Dy, Eu and Yb. With the aid of these colorants and fluorescent agents a simple dying of the glass ceramic is possible in order to imitate the desired optical properties in particular of natural tooth material. It is surprising that this is possible without problems despite the low quartz present as further crystal phase.

In a preferred embodiment of the glass ceramic the molar ratio of S1O2 to L12O lies in the range of from 2.2 to 4.1, preferably 2.2 to 3.8 and particularly preferably 2.2 to 3.5. It is surprising that the preparation of the glass ceramic according to the invention with lithium silicate as main crystal phase and low quartz as further crystal phase is achieved within these broad ranges.

The term main crystal phase refers to the crystal phase which has the highest proportion by mass of all the crystal phases present in the glass ceramic. The masses of the crystal phases

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- 10 are determined in particular using the Rietveld method. A suitable process for the quantitative analysis of the crystal phases by means of the Rietveld method is described e.g. in M. Dittmer's doctoral thesis Glasses and glass ceramics in the MgO-AlzCh-SiOz system with ZrO2 as nucleating agent, University of Jena 2011.

It is preferred that the glass ceramic according to the invention comprises lithium disilicate or lithium metasilicate as main.crystal phase. In a particularly preferred embodiment, the glass ceramic according to the invention comprises lithium disilicate as main crystal phase, as this glass ceramic has a particularly advantageous combination of desirable properties.

In the case of a glass ceramic according to the invention with lithium metasilicate as main crystal phase it is preferred that the glass ceramic also comprises lithium disilicate as further crystal phase in addition to low quartz.

It is preferred that the glass ceramic according to the invention has at least 20 wt.-%, preferably 25 to 55 wt.-% and particularly preferably 30 to 55 wt.-% lithium disilicate crystals.

It is further preferred that the glass ceramic according to the invention has 0.2 to 28 wt.-% and particularly preferably 0.5 to 25 wt.-% low quartz crystals.

The glass ceramic according to the invention can comprise, in addition to lithium silicate and low quartz, still further crystal phases, such as apatite, caesium aluminosilicate and in particular lithium phosphate. However, the amount of

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- 11 cristobalite should be as small as possible, and in particular should be less than 1.0 wt.-%. It is particularly preferred that the glass ceramic according to the invention is substantially free from cristobalite.

The type and in particular the amount of the crystal phases formed can be controlled by the composition of the starting glass as well as the heat treatment which is used to prepare the glass ceramic from the starting glass. The examples illustrate this with reference to the variation in the composition of the starting glass and the heat treatment used.

The glass ceramic has a high biaxial breaking strength of preferably at least 200 MPa and particularly preferably 250 to 460 MPa. The biaxial breaking strength was determined according to ISO 6872 (2008) (piston-on-three-ball test).

It is particularly surprising that, despite this high breaking strength, the glass ceramic according to the invention can be machined easily and quickly by means of computer-assisted milling and grinding apparatuses in order to give the glass ceramic e.g. the shape of a dental restoration.

The glass ceramic according to the invention has a coefficient of thermal expansion CTE (measured in the range of 100 to 500 °C) of preferably 9.5 to 14.0 ΊΟ-βΚ'¹. The CTE is determined according to ISO 6872 (2008). The coefficient of thermal expansion is adjusted to a desired value in particular by the type and amount of the crystal phases present in the glass ceramic as well as the chemical composition of the glass ceramic.

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- 12 The translucence of the glass ceramic was determined in the form of the contrast value (CR value) according to British Standard BS 5612, and this contrast value was preferably 40 to 92.

The particular combination of properties present in the case of the glass ceramic according to the invention even allows it to be used as dental material and in particular as material for the preparation of dental restorations.

The invention likewise relates to various precursors with a corresponding composition from which the lithium silicate-low quartz glass ceramic according to the invention can be prepared by heat treatment. These precursors are a starting glass with a corresponding composition and a starting glass with nuclei with a corresponding composition. The term corresponding composition means that these precursors comprise the same components in the same amounts as the glass ceramic, wherein the components with the exception of fluorine are calculated as oxides, as is usual for glasses and glass ceramics.

The invention therefore also relates to a starting glass which comprises the components of the lithium disilicate-low quartz glass ceramic according to the invention.

The starting glass according to the invention therefore comprises in particular suitable amounts of S1O2 and L12O which are required to form the glass ceramic according to the invention with lithium silicate as main crystal phase and low quartz as further crystal phase. Further, the starting glass can also comprise still other components, such as are specified above for the lithium silicate-low quartz glass ceramic according to the invention. All those embodiments which are specified as preferred for the components of the lithium silicate-low quartz glass ceramic according to the

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- 13 invention are also preferred for the components of the starting glass.

The invention also relates to such a starting glass which comprises nuclei for the crystallization of lithium metasilicate, lithium disilicate and/or low quartz.

The further precursor starting glass with nuclei can be produced first by heat treatment of the starting glass. The lithium silicate-low quartz glass ceramic according to the invention can then be produced by heat treatment of this further precursor. It is preferred to form the lithium silicate-low quartz glass ceramic according to the invention by heat treatment of the starting glass with nuclei.

It is preferred to subject the starting glass to a heat treatment at a temperature of 400 to 600°C, in particular 450 to 550°C, for a period of preferably 5 to 120 min, in particular 10 to 60 min, in order to produce the starting glass with nuclei for the crystallization of lithium metasilicate, lithium disilicate and/or low quartz.

It is further preferred to subject the starting glass with nuclei to a heat treatment at a temperature of 700 to 900°C for a period of in particular 1 to 120 min, preferably 5 to 120 min, particularly preferably 10 to 60 min, in order to prepare the lithium silicate-low quartz glass ceramic. To prepare the lithium silicate-low quartz glass ceramic the heat treatment of the starting glass with nuclei particularly preferably takes place at 700 to 880°C, in particular 750 to 850°C, for a period of preferably 5 to 120 min, particularly preferably 10 to 60 min.

The invention also relates to a process for the preparation of the lithium silicate-low quartz glass ceramic according to the invention, in which the starting glass or the starting glass with nuclei is subjected to at least one heat treatment at a

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- 14 temperature of 700 to 900°C for a period of in particular 1 to 120 min, preferably 5 to 120 min and particularly preferably 10 to 60 min.

The starting glass and the starting glass with nuclei can be subjected to the at least one heat treatment e.g. in the form of a solid glass blank, a powder compact or a powder.

The at least one heat treatment carried out in the process according to the invention can also take place during a hot pressing or sintering-on of the starting glass according to the invention or of the starting glass with nuclei according to the invention.

In a preferred embodiment the process according to the invention comprises (a) the heat treatment of the starting glass at a temperature of 400 to 600°C in order to form the starting glass with nuclei, and (b) the heat treatment of the starting glass with nuclei at a temperature of 700 to 900°C in order to form the lithium silicate-low quartz glass ceramic.

The duration of the heat treatments carried out in (a) and (b) is in particular 5 to 120 min and preferably 10 to 60 min.

To prepare the starting glass, the procedure is in particular that a mixture of suitable starting materials, such as carbonates, oxides, phosphates and fluorides, is melted at temperatures of in particular 1300 to 1600°C for 2 to 10 h. To achieve a particularly high homogeneity, the obtained glass melt is poured into water in order to form a granular glass material, and the obtained granulate is then melted again.

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- 15 The melt can then be poured into moulds in order to produce blanks of the starting glass, so-called solid glass blanks or monolithic blanks.

It is also possible to put the melt into water again in order to prepare a granulate. This granulate can be pressed, after grinding and optionally addition of further components, such as colorants and fluorescent agents, to form a blank, a so-called powder compact.

Finally, the starting glass can also be processed to form a powder after granulation.

The starting glass, e.g. in the form of a solid glass blank, a powder compact or in the form of a powder, is then subjected to at least one heat treatment. It is preferred that a first heat treatment is carried out first in order to prepare a starting glass according to the invention with nuclei which are suitable for forming lithium metasilicate, lithium disilicate and/or low quartz crystals. The glass with nuclei is then usually subjected to at least one further temperature treatment at a higher temperature in order to effect crystallization of lithium silicate, in particular of lithium disilicate, and low quartz.

The glass ceramics according to the invention and the glasses according to the invention are present in particular in the form of powders, granulates or blanks of any shape and size, e.g. monolithic blanks, such as platelets, cuboids or cylinders, or powder compacts, in unsintered, partially sintered or densely sintered form. They can easily be further processed in these forms. They can, however, also be present in the form of dental restorations, such as inlays, onlays, crowns, veneers, facets or abutments.

Dental restorations, such as bridges, inlays, onlays, crowns, veneers, facets or abutments, can be prepared from the glass ceramics according to the invention and the glasses according

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- 16 to the invention. The invention therefore also relates to their use for the preparation of dental restorations. It is preferred that the glass ceramic or the glass is given the shape of the desired dental restoration by pressing or machining.

The pressing is usually carried out under increased pressure and at increased temperature. It is preferred that the pressing is carried out at a temperature of 700 to 1200°C. It is further preferred to carry out the pressing at a pressure of 2 to 10 bar. During pressing, the desired change in shape is achieved by viscous flow of the material used. The starting glass according to the invention and in particular the starting glass with nuclei according to the invention, and the lithium silicate-low quartz glass ceramic according to the invention, can be used for the pressing. The glasses and glass ceramics according to the invention can be used in particular in the form of blanks in any shape and size, e.g. solid blanks or powder compacts, e.g. in unsintered, partially sintered or densely sintered form.

The machining is usually carried out by material removal processes and in particular by milling and/or grinding. It is particularly preferred that the machining is carried out during a CAD/CAM process. The starting glass according to the invention, the starting glass with nuclei according to the invention and the lithium silicate-low quartz glass ceramic according to the invention can be used for the machining. The glasses and glass ceramics according to the invention can be used in particular in the form of blanks, e.g. solid blanks or powder compacts, e.g. in unsintered, partially sintered or densely sintered form. The lithium silicate-low quartz glass ceramic according to the invention is preferably used for the machining.

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- 17 treated in order to reduce the porosity, e.g. of a porous powder compact used.

However, the glass ceramics according to the invention and the glasses according to the invention are also suitable as coating material for e.g. ceramics and glass ceramics. The invention is therefore also directed towards the use of the glasses according to the invention or the glass ceramics according to the invention for coating in particular ceramics and glass ceramics.

The invention also relates to a process for coating ceramics, metals, metal alloys and glass ceramics, in which glass ceramic according to the invention or glass according to the invention is applied to the ceramic or glass ceramic and exposed to increased temperature.

This can be carried out in particular by sintering-on or joining of an overstructure prepared by means of CAD/CAM using a suitable glass solder or adhesive, and preferably by pressingon. In the case of sintering-on, the glass ceramic or the glass is applied to the material to be coated, such as ceramic or glass ceramic, in the usual way, e.g. as a powder, and then sintered at increased temperature. In the case of the preferred pressing-on, glass ceramic according to the invention or glass according to the invention is pressed on, e.g. in the form of powder compacts or monolithic blanks, at an increased temperature of e.g. 700 to 1200°C, and with the application of pressure, e.g. 2 to 10 bar. For this, in particular the processes described in EP 231 773 and the press furnace disclosed there can be used. A suitable furnace is e.g. the Programat EP 5000 from Ivoclar Vivadent AG, Liechtenstein.

It is preferred that, after conclusion of the coating process, the glass ceramic according to the invention is present with lithium silicate, in particular lithium disilicate, as main

CA 02995309 2019-02-09 crystal phase and low quartz as further crystal phase, as such

- 18 a glass ceramic has particularly good properties.

Because of the above-described properties of the glass ceramics according to the invention and the glasses according to the invention, these are suitable in particular for use in dentistry. A subject of the invention is therefore also the use of the glass ceramics according to the invention or the glasses according to the invention as dental material and in particular for the preparation of dental restorations or as coating material for dental restorations, such as crowns, bridges and abutments.

The invention is explained in more detail below with reference to non-limiting examples.

Examples

Examples 1 to 34 - Composition and crystal phases

A total of 34 glasses and glass ceramics according to the invention with the composition specified in Table Î were prepared by melting corresponding starting glasses as well as subsequent heat treatments for controlled nucleation and crystallization.

The heat treatments used for controlled nucleation and controlled crystallization are also specified in Table I. The following meanings apply

T_g Glass transition temperature, determined by means of DSC

Ts and ts

Temperature and time used for melting the starting glass

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<td></td><td> - 19 -</td>

<td> Txb and tsb</td><td> Temperature and time used for nucleation of the starting glass</td>

<td> Tc and t_c</td><td> Temperature and time used for the crystallization</td>

<td> Tpress and tpress</td><td> Temperature and time used for crystallization by hot pressing</td>

<td> CR value</td><td> Contrast value of the glass ceramic according to British Standard BS 5612 determined using: Apparatus: CM-3700d spectrometer (KonicaMinolta) Measurement parameters : Measurement area: 7 nun x 5 mm Type of measurement: reflectance / reflection Measurement range: 400 nm - 700 nm Sample size: Diameter: 15-20 mm Thickness: 2 nun +/- 0.025 nun Plane parallelism: +/- 0.05 mm Surface roughness: about 18 pm.</td>

<td> CTE</td><td> Coefficient of thermal expansion of the glass ceramic according to ISO 6872 (2008), measured in the range of 100 to 500°C</td>

<td> Cfeiax</td><td> Biaxial breaking strength, measured according to dental standard ISO 6872 (2008)</td>

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- 20 The amounts of the crystal phases were determined by means of the Rietveld method. For this, powders of the respective glass ceramic were used which were mixed with AI2O3 (product name: Taimicron TM-DAR, from: Taimei Chemicals, Co. Ltd., Japan) as internal standard in a ratio of 50 wt.-% glass ceramic to 50 wt.-% AI2O3. This mixture was slurried with acetone in order to achieve as good a thorough mixing as possible. The mixture was then dried at about 80°C. Then a diffractogram in the range 10 to 100° 2Θ was acquired by means of a D8 Advance diffractometer from Bruker using Cu;&lt;_a radiation and a step size of 0.014° 2Θ. This diffractogram was then evaluated with the TOPAS software from Bruker, and the phase proportions were determined. For all diffractograms a lower limit of about 30 nm for the L13PO4 crystallite size was used.

To produce the glasses and glass ceramics according to the invention the starting glasses in a range of 100 to 200 g were first melted from customary raw materials at 1500°C or 1400°C for a period of 1 to 3 hours, wherein the melting was very easily possible without formation of bubbles or streaks. By pouring the starting glasses into water, glass frits were prepared which were then melted a second time at 1500°C or 1400°C for 1 hour for homogenization.

A first heat treatment of the starting glasses at a temperature of 460 to 550°C led to the formation of glasses with nuclei. As a result of a further heat treatment at 760 to 880°C, these nuclei-containing glasses crystallized to form glass ceramics with lithium silicate as main crystal phase and low quartz as further crystal phase, as was established by X-ray diffraction tests. Thus, lithium silicate-low quartz glass ceramics according to the invention were obtained.

A) Solid glass blocks

In Examples 1-26, 28 and 31-34 the glass ceramics were prepared from solid glass blocks. For this, the obtained glass granulates

CA 02995309 201S-02-09

- 21 were melted again at the temperature Ts for a period ts. The obtained melts of the starting glass were then poured into a graphite mould in order to produce solid glass blocks. These glass monoliths were then stress relieved at the temperature Tub for a period tta» whereby nucleation was able to take place. The nuclei-containing starting glasses were then heated to a temperature Tc for a period tc. Glass ceramics according to the invention with lithium disilicate as main crystal phase and low quartz as additional phase were thereby formed, as could be established by X-ray diffraction tests at room temperature.

It is assumed that in this process variant a volume crystallization of lithium disilicate and low quartz has taken place.

B) Powder compacts

In Example 27 the glass ceramic was prepared from powder compacts. For this, the obtained glass granulate was ground in a zirconium oxide mill to a particle size of &lt; 90 pm. About 4 g of this powder was then pressed to form cylindrical blanks and sintered in a sinter furnace (Programat® from Ivoclar Vivadent AG) at a temperature Tc and a holding time of tc to form dense glass ceramic bodies. A glass ceramic according to the invention with lithium metasilicate as main crystal phase as well as lithium disilicate and low quartz as additional phases was formed by the sintering, as could be established by X-ray diffraction tests at room temperature.

C) Preparation of a dental restoration from blocks according to A)

CA 02995309 2019-02-09

- 22 The glass ceramic blocks produced according to Examples 1-26, 28 and 31-34 were machined in a CAD/CAM unit to form desired dental restorations, such as crowns. For this, the crystallized blocks were provided with a suitable holder, and then given the desired shape in an inLab MC XL grinding unit from Sirona Dental GmbH, Germany. For the processing of the blanks according to the invention it was possible to use the same grinding parameters as for commercial e.max CAD blocks, Ivoclar Vivadent, Liechtenstein.

D) Hot pressing of the glass ceramic

In Example 19, for which T_Pr_ess and t_press are specified, the glass ceramic was prepared from solid glass blocks by hot pressing.

For this, the obtained glass granulate was melted again at the temperature Ts for a period ts. The obtained melt of the starting glass was then poured into a pre-heated steel mould in order to produce rods. These monolithic glass rods were then stress relieved at a temperature Tra, for a period txt, whereby nucleation was able to take place. The rods were then sawn to form small cylinders with a mass of about 4 to 6 g. These small cylinders were then crystallized at a temperature T_c for a period of t_c. The nucleated and crystallized cylinders were then pressed to form a shaped body in a hot-pressing furnace at the temperature Tpress and for a holding time of tpress· A glass ceramic according to the invention with lithium disilicate as main crystal phase and low quartz as further crystal phase had formed after the hot-pressing, as could be established by X-ray diffraction tests of the formed shaped body at room temperature.

E) Sintering of a nucleated glass

CA 02995309 2010-02-09

- 23 In Example 29 the starting glass was melted at 1500°C for 2 h and then quenched in water. The obtained glass granulate was then nucleated at a temperature Tkh and for a time tja>. The nucleated starting glass was comminuted to form a powder with an average particle size of 20 um. A test piece was prepared from this nucleated glass powder to determine the thermal expansion and to determine the optical properties, and crystallized and densely sintered at a temperature of T_c and 10 for a time tc. After the dense sintering a glass ceramic according to the invention with lithium disilicate as main crystal phase and low quartz as further additional phase had formed, as could be established by X-ray diffraction tests of the formed shaped body at room temperature.

CA 02995309 2010-02-09

- 24 Table 1

<td> Example NO.</td><td> 1</td><td> 2</td><td> 3</td><td> 4</td><td> 5</td>

<td> Composition</td><td> wt.-%</td><td> wt-%</td><td> wt-%</td><td> wt-%</td><td> wt-%</td>

<td> SiOa</td><td> 74.3</td><td> 73.3</td><td> 72.0</td><td> 72.0</td><td> 74.9</td>

<td> UaO</td><td> 11.2</td><td> 12.6</td><td> 13.3</td><td> 12.3</td><td> 10.7</td>

<td> KaO</td><td> 3.4</td><td> 3.2</td><td> 3.5</td><td> 3.4</td><td> 3.4</td>

<td> RbaO</td><td> -</td><td> •</td><td> -</td><td> -</td><td></td>

<td> MgO</td><td> 4.4</td><td> 1.4</td><td> 4.5</td><td> 4.4</td><td> 4.4</td>

<td> CaO</td><td> -</td><td> 1.9</td><td> •</td><td> .</td><td> -</td>

<td> SrO</td><td> •</td><td> •</td><td> -</td><td> -</td><td> -</td>

<td> AJ2O3</td><td> 2.8</td><td> 3.5</td><td> 2.8</td><td> 2.8</td><td> 2.8</td>

<td> GazOa</td><td> •</td><td> -</td><td> -</td><td> •</td><td> -</td>

<td> EraOa</td><td> -</td><td> -</td><td> -</td><td> 0.1</td><td></td>

<td> CeOa</td><td> -</td><td> -</td><td> -</td><td> 0.8</td><td> -</td>

<td> V2O5</td><td> •</td><td> •</td><td> -</td><td> 0.1</td><td> -</td>

<td> P2O5</td><td> 3.9</td><td> 4.1</td><td> 3.9</td><td> 3.9</td><td> 3.8</td>

<td> P</td><td> •</td><td> •</td><td> -</td><td> •</td><td></td>

<td> TtuOr</td><td> -</td><td> -</td><td> -</td><td> 0.3</td><td> -</td>

<td> Tg/’C</td><td> 471</td><td> 465</td><td> 469</td><td> 463</td><td> 471</td>

<td> Ts/°C, ts/min</td><td> 1500,120</td><td> 1520,120</td><td> 1500,120</td><td> 1500,120</td><td> 1500,120</td>

<td> Tra&gt;/^sC, Wmh</td><td> 500,30</td><td> 480,10</td><td> 500,30</td><td> 500,30</td><td> 500,30</td>

<td> Te/“C, tc/min</td><td> 800,30</td><td> 800,15</td><td> 800,30</td><td> 810,20</td><td> 800,30</td>

<td> Main crystal phase (wt-%)</td><td> LiaSiaOs (40.9)</td><td> LiaSiaOs</td><td> LiaSiaOs (51.3)</td><td> LiaSiaOs (43.4)</td><td> LiaSiaOs (36.2)</td>

<td> Further crystal phases (wt.-%)</td><td> Low quartz (17.5), Ü3PO4 (6.3)</td><td> Low quartz, U3PO4</td><td> Low quartz (0.2), IJ3PO4 (6.8)</td><td> Low quartz (4-4), U3PO4 (6.0),</td><td> Low quartz (20.7), U3PO4 (5.4)</td>

<td> OBiw/MPa</td><td> 464</td><td></td><td></td><td> 376</td><td></td>

<td> CR value</td><td> 71.83</td><td></td><td></td><td> 71.45</td><td> 71.21</td>

<td> L*</td><td> 94.15</td><td></td><td></td><td> 89.46</td><td> 93.90</td>

<td> a*</td><td> -0.45</td><td></td><td></td><td> 0.48</td><td> -0.40</td>

<td> b*</td><td> 3.44</td><td></td><td></td><td> 13.22</td><td> 3.92</td>

<td> CTE/10«K-¹ (100- 500’C)</td><td></td><td></td><td></td><td></td><td></td>

CA 02995309 2019-02-09

- 25 Table I (continued)

<td> Example No.</td><td> 6</td><td> 7</td><td> 8</td><td> 9</td><td> 10</td>

<td> Composition</td><td> wt.-%</td><td> wt.-%</td><td> wt.-%</td><td> wt.-%</td><td> wt.-%</td>

<td> Si02</td><td> 72.3</td><td> 72.6</td><td> 70.1</td><td> 73.0</td><td> 75.6</td>

<td> LiaO</td><td> 12.0</td><td> 11.7</td><td> 11.3</td><td> 11.4</td><td> 10.2</td>

<td> K2O</td><td> 3.4</td><td> 3.4</td><td> .</td><td> 3.4</td><td> 3.4</td>

<td> RbaO</td><td> -</td><td> -</td><td> 6.5</td><td> .</td><td> •</td>

<td> MgO</td><td> 4.4</td><td> 4.4</td><td> 4.2</td><td> 4.4</td><td> 4.3</td>

<td> CaO</td><td> • -</td><td> -</td><td> -</td><td> -</td><td> .</td>

<td> SrO</td><td> -</td><td> -</td><td> •</td><td> .</td><td> •</td>

<td> AI2O3</td><td> 2.8</td><td> 2.8</td><td> 2.2</td><td> 2.8</td><td> 2.7</td>

<td> GaaOa</td><td> -</td><td> -</td><td> -</td><td> .</td><td> •</td>

<td> Erath</td><td> 0.1</td><td> 0.1</td><td> 0.1</td><td> 0.1</td><td></td>

<td> CeOa</td><td> 0.8</td><td> 0.8</td><td> 0.7</td><td> 0.6</td><td></td>

<td> VaOs</td><td> 0.1</td><td> 0.1</td><td> 0.1</td><td> 0.1</td><td></td>

<td> P2O5</td><td> 3.9</td><td> 3.8</td><td> 4.5</td><td> 3.8</td><td> 3.8</td>

<td> P</td><td> -</td><td> -</td><td> •</td><td> -</td><td> .</td>

<td> TbcO?</td><td> 0.3</td><td> 0.3</td><td> 0.3</td><td> 0.4</td><td> -</td>

<td> Tg/°C</td><td> 469</td><td> 473</td><td> 472</td><td> 470</td><td> 480</td>

<td> Ts/’C, ts/min</td><td> 1500,120</td><td> 1500,120</td><td> 1500,120</td><td> 1500,120</td><td> 1500,120</td>

<td> Ti&lt;b/^eC, tKb/mii</td><td> 480,60</td><td> 520,10</td><td> 480,120</td><td> 470,10</td><td> 500,30</td>

<td> T_c/°C, tc/min</td><td> 800,30</td><td> 820,10</td><td> 800,10</td><td> 780,30</td><td> 800,30</td>

<td> Mari crystal phase (wt.-%)</td><td> UaSiaOs (42.7)</td><td> LiaSiaOs (39.0)</td><td> UaSiaOs (30.0)</td><td> UaSiaOs (38.4)</td><td> UaSiaOs (32.7)</td>

<td> Further crystal phases (wt-%)</td><td> Low quartz (10.2), U3PO4 (6.0)</td><td> Low quartz (12.1), U3PO4 (6.0)</td><td> Low quartz (7.1). UsPOaP.D</td><td> Low quartz (14.8), LfePO* (5.6)</td><td> Low quartz (24.2), U3PO4 (6.3)</td>

<td> Ote»/MPa</td><td> 371</td><td> 395</td><td> 456</td><td> 326</td><td> 347</td>

<td> CR value</td><td> 69.27</td><td> 68.94</td><td> 77.14</td><td> 68.63</td><td> 71.28</td>

<td> L*</td><td> 89.78</td><td> 89.68</td><td> 90.06</td><td> 90.29</td><td> 94.07</td>

<td> a*</td><td> 0.34</td><td> 0.18</td><td> -0.13</td><td> 0.85</td><td> -0.46</td>

<td> b*</td><td> 13.65</td><td> 13.9</td><td> 9.07</td><td> 11.17</td><td> 3.46</td>

<td> CTE/Km¹ (100- 500°C)</td><td> 10.8</td><td> 11.3</td><td></td><td> 11.5</td><td></td>

CA 02995309 2010-02-09

- 26 Table I (continued)

<td> Example No.</td><td> 11</td><td> 12</td><td> 13</td><td> 14</td><td> 15</td>

<td> Composition</td><td> wt-%</td><td> wt-%</td><td> wt-%</td><td> wt.-%</td><td> wt.-%</td>

<td> SiOz</td><td> 72.9</td><td> 72.2</td><td> 70.2</td><td> 72.4</td><td> 70.4</td>

<td> LizO</td><td> 11.3</td><td> 11.6</td><td> 12.5</td><td> 10.9</td><td> 12.1</td>

<td> KzO</td><td> 2.1</td><td> 3.4</td><td> 3.3</td><td> 3.4</td><td> 3.1</td>

<td> RbzO</td><td> •</td><td> -</td><td> •</td><td> -</td><td> -</td>

<td> MgO</td><td> 1.8</td><td> 4.4</td><td> 1.6</td><td> 4.3</td><td> 3.4</td>

<td> CaO</td><td> 1.8</td><td> -</td><td> 2.3</td><td> •</td><td> .</td>

<td> SrO</td><td> 3.3</td><td> •</td><td> -</td><td> -</td><td> •</td>

<td> AbOs</td><td> 2.7</td><td> 4.6</td><td> 4.0</td><td> 3.9</td><td> 3.6</td>

<td> GazOs</td><td> -</td><td> -</td><td> •</td><td> -</td><td> 2.5</td>

<td> ErzOa</td><td> -</td><td> -</td><td> 0.2</td><td> 0.2</td><td> 0.1</td>

<td> CeOz</td><td> -</td><td> •</td><td> 1.2</td><td> 0.6</td><td> 0.9</td>

<td> VzOs</td><td> -</td><td> -</td><td> 0.1</td><td> 0.1</td><td> 0.1</td>

<td> PzOs</td><td> 3.8</td><td> 3.8</td><td> 4.3</td><td> 3.8</td><td> 3.5</td>

<td> F-</td><td> 0.3</td><td> -</td><td> •</td><td> -</td><td> -</td>

<td> Tb«O?</td><td> •</td><td> -</td><td> 0.3</td><td> 0.4</td><td> 0.3</td>

<td> Tg ! °C</td><td> 453</td><td> 477</td><td> 464</td><td> 472</td><td> 462</td>

<td> Ts/’C.ts/min</td><td> 1500,120</td><td> 1500,120</td><td> 1500,120</td><td> 1500,120</td><td> 1500,120</td>

<td> TKb/'C.Wmin</td><td> 460,90</td><td> 500,30</td><td> 500,10</td><td> 480,40</td><td> 540,10</td>

<td> Tc/°C, tc/min</td><td> 800,40</td><td> 800,30</td><td> 800,60</td><td> 770,60</td><td> 790,30</td>

<td> Main crystal phase (wt-%)</td><td> LizSizOs (45.0)</td><td> LizSizOs (38.7)</td><td> LizSizOs (38.1)</td><td> LizSizOs (34.4)</td><td> LizSizOs (39.0)</td>

<td> Further crystal phases (wt-%)</td><td> Low quartz (19.3), U3PO4 (2.8). CazSra(PO«)aF (5.5)</td><td> Low quartz (13.4), UaPOa (5.4)</td><td> Low quartz (9.4), U3PO4 (6.3)</td><td> Low quartz (17.4), U3PO4 (5.2)</td><td> Low quartz (9.9), U3PO4 (5.4)</td>

<td> osax/MPa</td><td> 397</td><td></td><td> 350</td><td> 377</td><td> 285</td>

<td> CR value</td><td> 70.06</td><td></td><td> 64.56</td><td> 69.01</td><td> 70.84</td>

<td> L*</td><td> 89.22</td><td></td><td> 85.82</td><td> 90.67</td><td> 86.98</td>

<td> a*</td><td> 0.50</td><td></td><td> 2.6</td><td> 1.95</td><td> 1.80</td>

<td> b*</td><td> 5.87</td><td></td><td> 19.74</td><td> 8.96</td><td> 19.10</td>

<td> CTE/10*K·¹ (100500’C)</td><td></td><td></td><td> 10.6</td><td> 10.8</td><td></td>

CA 02995309 2019-02-09

Table I (continued)

<td> Example No.</td><td> 16</td><td> 17</td><td> 18</td><td> 19</td><td> 20</td>

<td> Composition</td><td> wt.-%</td><td> wt.-%</td><td> wt.-%</td><td> wt-%</td><td> wt-%</td>

<td> SiOs</td><td> 69.2</td><td> 71.5</td><td> 71.0</td><td> 74.7</td><td> 70.0</td>

<td> LiaO</td><td> 11.5</td><td> 10.5</td><td> 10.0</td><td> 9.8</td><td> 10.5</td>

<td> KaO</td><td> 3.2</td><td> 3.3</td><td> 3.3</td><td> 3.3</td><td> 3.2</td>

<td> CS2O</td><td> •</td><td> -</td><td> -</td><td> .</td><td></td>

<td> RbaO</td><td> -</td><td> -</td><td> -</td><td> -</td><td></td>

<td> MgO</td><td> 3.1</td><td> 3.5</td><td> 3.8</td><td> 4.3</td><td> 3.8</td>

<td> CaO</td><td> -</td><td> -</td><td> •</td><td> •</td><td> •</td>

<td> SrO</td><td> •</td><td> •</td><td> •</td><td> •</td><td> •</td>

<td> ZnO</td><td> •</td><td> -</td><td> .</td><td></td><td> «</td>

<td> AI2O3</td><td> 3.1</td><td> 2.8</td><td> 3.0</td><td> 2.9</td><td> 38</td>

<td> GajOa</td><td> -</td><td> •</td><td></td><td> .</td><td> •</td>

<td> LasO?</td><td> -</td><td> -</td><td> 3.4</td><td> •</td><td> «</td>

<td> Y2O3</td><td> •</td><td> 2.9</td><td> •</td><td> •</td><td></td>

<td> InzOs</td><td> 4.7</td><td> -</td><td> -</td><td> .</td><td></td>

<td> EraOa</td><td> 0.2</td><td> 0.1</td><td> 0.1</td><td> 0.1</td><td> 0.2</td>

<td> ZrO₂</td><td> •</td><td> -</td><td> .</td><td></td><td> .</td>

<td> SnOa</td><td></td><td> -</td><td> .</td><td> -</td><td></td>

<td> CeOa</td><td> 1.0</td><td> 0.6</td><td> 1.2</td><td> 0.8</td><td> 0.5</td>

<td> MnOa</td><td> -</td><td> -</td><td> •</td><td> •</td><td> -</td>

<td> VaO₅</td><td> 0.1</td><td> 0.1</td><td> 0.1</td><td> 0.1</td><td> 0.1</td>

<td> TaaOs</td><td> •</td><td> .</td><td> .</td><td></td><td> 3.8</td>

<td> P₂o₅</td><td> 3.5</td><td> 4.3</td><td> 3.7</td><td> 3.6</td><td> 3.7</td>

<td> F</td><td> •</td><td> •</td><td> •</td><td> •</td><td> •</td>

<td> TtxOr</td><td> 0.4</td><td> 0.4</td><td> 0.4</td><td> 0.4</td><td> 0.4</td>

<td> Tg/°C</td><td> 483</td><td> 477</td><td> 478</td><td> 467</td><td> 482</td>

<td> Ts/^eC,ts/min</td><td> 1500,120</td><td> 1500,120</td><td> 1500,1«)</td><td> 1500,120</td><td> 1500,120</td>

<td> Tko/’C, Wmin</td><td> 550,30</td><td> 480,10</td><td> 500,40</td><td> 470,60</td><td> 500,20</td>

<td> Tç/’C.tc/min</td><td> 770,20</td><td> 760,10</td><td> 760,20</td><td> 750,30</td><td> 760,30</td>

<td> Tprass / °C, tprass I °C</td><td></td><td></td><td></td><td> 870,25</td><td></td>

<td> Main crystal phase (wt-%)</td><td> LiaSiaOs (32.4)</td><td> LiaSiaOs (27.0)</td><td> LiaSiaOs (27.3)</td><td> LiaSiaOs (28.8)</td><td> LiaSiaOs (29.1)</td>

<td> Further crystal phases (wt-%)</td><td> Lew quartz (98), UaPCh (4.9),</td><td> Low quartz (19.9), U3PO4 (6.0)</td><td> Low quartz (18.6), U3PO4 (5.1)</td><td> Low quartz (24.3), U3PO4 (3.8)</td><td> Low quartz (14.8). U3PO4 (4.4)</td>

<td> OBiax/MPa</td><td> 299</td><td> 290</td><td> 320</td><td></td><td> 367</td>

<td> CR value</td><td> 57.60</td><td> 56.69</td><td> 46.84</td><td> 64.29</td><td> 63.10</td>

<td> L*</td><td> 85.77</td><td> 90.49</td><td> 84.38</td><td> 90.6</td><td> 89.91</td>

<td> a*</td><td> 0.16</td><td> -0.50</td><td> 0.05</td><td> 0.38</td><td> 1.70</td>

<td> b*</td><td> 19.18</td><td> 9.68</td><td> 26.72</td><td> 12.76</td><td> 9.43</td>

<td> CTE/10«K·¹ (100500°C)</td><td></td><td></td><td></td><td> 12.8</td><td></td>

CA 02995309 2019-02-09

- 28 Table I (continued)

<td> Example No.</td><td> 21</td><td> 22</td><td> 23</td><td> 24</td><td> 25</td>

<td> Composition</td><td> _ wt-%</td><td> wt-%</td><td> wt-%</td><td> wt-%</td><td> wt-%</td>

<td> SiOz</td><td> 72.9</td><td> 68.8</td><td> 69.5</td><td> 73.2</td><td> 73.7</td>

<td> UzO</td><td> 12.5</td><td> 11.4</td><td> 11.5</td><td> 11.7</td><td> 11.5</td>

<td> KzO</td><td> 3.5</td><td> 3.3</td><td> 3.3</td><td> 0.8</td><td> 3.3</td>

<td> CszO</td><td></td><td> •</td><td> .</td><td> 1.3</td><td></td>

<td> RbzO</td><td></td><td> .</td><td> .</td><td> 1.3</td><td></td>

<td> MgO</td><td> 4.4</td><td> 3.2</td><td> 1.1</td><td> 2.9</td><td></td>

<td> CaO</td><td></td><td> -</td><td> 1.5</td><td> •</td><td></td>

<td> SrO</td><td></td><td> -</td><td> 2.4</td><td></td><td> 3.6</td>

<td> ZnO</td><td></td><td> •</td><td> 1.8</td><td> .</td><td></td>

<td> AI2O3</td><td> 2.8</td><td> 3.2</td><td> 2.7</td><td> 2.7</td><td> 2.5</td>

<td> GazOs</td><td></td><td> -</td><td> •</td><td> .</td><td></td>

<td> LazOa</td><td></td><td> -</td><td> -</td><td> .</td><td></td>

<td> Y2O3</td><td></td><td> •</td><td> .</td><td></td><td></td>

<td> InzOs</td><td></td><td> -</td><td> .</td><td></td><td> •</td>

<td> ErzOs</td><td></td><td> 0.2</td><td> 0.2</td><td> 0.1</td><td> 0.1</td>

<td> ZrOz</td><td></td><td> 2.1</td><td> .</td><td> .</td><td></td>

<td> SnOz</td><td></td><td> 2.6</td><td> •</td><td> .</td><td></td>

<td> CeOz</td><td></td><td> 1.1</td><td> 1.8</td><td> 1.5</td><td> 1.5</td>

<td> MnOz</td><td></td><td> •</td><td> .</td><td> 0.1</td><td></td>

<td> VzOs</td><td></td><td> 0.1</td><td> 0.2</td><td> 0.2</td><td> 0.1</td>

<td> TazOs</td><td></td><td> .</td><td> •</td><td> .</td><td></td>

<td> PzO₅</td><td> 3.9</td><td> 3.6</td><td> 3.7</td><td> 3.8</td><td> 3.3</td>

<td> F</td><td></td><td> .</td><td> -</td><td> •</td><td></td>

<td> Tb«O?</td><td></td><td> 0.4</td><td> 0.3</td><td> 0.4</td><td> 0.4</td>

<td> Tg/’C</td><td> 473</td><td> 483</td><td> 461</td><td> 467</td><td> 472</td>

<td> Ts/’C.ts/min</td><td> 1500,120</td><td> 1500,120</td><td> 1500,120</td><td> 1500.120</td><td> 1500,120</td>

<td> Tw&gt; / °C, tko/ min</td><td> 500,30</td><td> 490,30</td><td> 480,30</td><td> 500,20</td><td> 500,70</td>

<td> T_c/’C,tc/min</td><td> 000,30</td><td> 770,40</td><td> 800,10</td><td> 820,30</td><td> 830,40</td>

<td> Tprase / Ό, tpræs / °C</td><td></td><td></td><td></td><td></td><td></td>

<td> Main crystal phase (wt-%)</td><td> LizSizOs (48.0)</td><td> LizSizOs</td><td> LizSizOs</td><td> LizSizOs</td><td> LizSizOs (37.3)</td>

<td> Further crystal phases (wt-%)</td><td> Low quartz (6.5). Ü3PO4 (6.6).</td><td> Low quartz, U3PO4</td><td> Low quartz, IJ3PO4</td><td> Low quartz, U3PO4</td><td> Low quartz (14.7), U3PO4 (2.1)</td>

<td> ofeex/MPa</td><td></td><td></td><td> 487</td><td></td><td></td>

<td> CR value</td><td> 74.98</td><td></td><td> 53.15</td><td></td><td></td>

<td> L*</td><td> 94.16</td><td></td><td> 79.74</td><td></td><td></td>

<td> a*</td><td> -0.62</td><td></td><td> 3.58</td><td></td><td></td>

<td> b*</td><td> 3.40</td><td></td><td> 34.15</td><td></td><td></td>

<td> στΕ/ισ«κ·'(ΐθο- 500°C)</td><td></td><td></td><td></td><td></td><td></td>

CA 02995309 2019-02-09

- 29 Table I (continued)

<td> Example No.</td><td> 26</td><td> 27</td><td> 28</td><td> 29</td>

<td> Composition</td><td> wt.-%</td><td> wt-%</td><td> wt.-%</td><td> wt.-%</td>

<td> SiO₂</td><td> 73.0</td><td> 74.8</td><td> 68.9</td><td> 75.8</td>

<td> LiaO</td><td> 11.7</td><td> 13.3</td><td> 12.2</td><td> 10.5</td>

<td> KaO</td><td> 3.4</td><td> 3.6</td><td> 3.3</td><td> 3.4</td>

<td> CsaO</td><td> -</td><td></td><td> -</td><td></td>

<td> RbsO</td><td> •</td><td> .</td><td> •</td><td> .</td>

<td> MgO</td><td> 4.4</td><td> 1.7</td><td> 1.4</td><td> 3.6</td>

<td> CaO</td><td> -</td><td> 2.4</td><td> 2.1</td><td> .</td>

<td> SrO</td><td> •</td><td></td><td> •</td><td> .</td>

<td> ZnO</td><td> -</td><td></td><td> -</td><td> .</td>

<td> AlaOa</td><td> 3.7</td><td> 4.2</td><td> 3.9</td><td> 2.9</td>

<td> GaaOa</td><td> •</td><td></td><td> •</td><td> -</td>

<td> LaaOa</td><td> -</td><td></td><td> -</td><td> •</td>

<td> YaOa</td><td> -</td><td></td><td> •</td><td> -</td>

<td> InaOa</td><td> .</td><td></td><td></td><td> -</td>

<td> EraOa</td><td> .</td><td></td><td> •</td><td></td>

<td> ZrOa</td><td> -</td><td></td><td> -</td><td> -</td>

<td> SnOa</td><td> •</td><td></td><td> .</td><td> -</td>

<td> CeOa</td><td> -</td><td></td><td> .</td><td></td>

<td> MnOa</td><td> •</td><td></td><td> .</td><td></td>

<td> VaOs</td><td></td><td></td><td> .</td><td> -</td>

<td> TaaOs</td><td> -</td><td></td><td> .</td><td> -</td>

<td> PaOs</td><td> 3.8</td><td></td><td> 8.2</td><td> 3.8</td>

<td> P</td><td> •</td><td></td><td> •</td><td></td>

<td> TbxO?</td><td> -</td><td></td><td></td><td> -</td>

<td> Tg/’C</td><td></td><td> 457</td><td> 471</td><td> 469</td>

<td> Ts/^eC, ts/min</td><td> 1500,120</td><td> 1500,180</td><td> 1500.150</td><td> 1500,120</td>

<td> Txb/’C.tKb/min</td><td> 500,30</td><td> •</td><td> 490,10</td><td> 500,30</td>

<td> Tc/’C,fc/min</td><td> 800,30</td><td> 780,10</td><td> 800,30</td><td> 880,1</td>

<td> Tprees / °C, tprees / °C</td><td></td><td></td><td></td><td></td>

<td> Main crystal phase (wt.-%)</td><td> LiaSiaOs (45.0)</td><td> LfeSiOa,</td><td> LiaSiaOs,</td><td> LiaSiaOs,</td>

<td> Further crystal phases (wt-%)</td><td> Low quartz (12.8), U3PO4 (6.0).</td><td> Low quartz, LiaSiaOs, U3PO4</td><td> Low quartz, LÎ3P04</td><td> Low quartz, U3PO4</td>

<td> era®/MPa</td><td></td><td></td><td> 320</td><td></td>

<td> CR value</td><td></td><td></td><td> 67.66</td><td> 76.6</td>

<td> L*</td><td></td><td></td><td> 91.17</td><td> 94</td>

<td> a*</td><td></td><td></td><td> 0.08</td><td> -0.21</td>

<td> b*</td><td></td><td></td><td> 4.69</td><td> 2.55</td>

<td> CTE/ 10-6K¹ (100- 500’C)</td><td></td><td></td><td></td><td> 12.3</td>

CA 02995309 2010-02-09

- 30 Table I (continued)

<td> Example No.</td><td> 30</td><td> 31</td><td> 32</td><td> 33</td><td> 34</td>

<td> Composition</td><td> wt.-%</td><td> wt-%</td><td> wt-%</td><td> wt-%</td><td> wt-%</td>

<td> SiOz</td><td> 64.4</td><td> 67.1</td><td> 69.8</td><td> 71.6</td><td> 59.7</td>

<td> U₂0</td><td> 14.6</td><td> 13.3</td><td> 11.9</td><td> 11.1</td><td> 12.9</td>

<td> NaaO</td><td> -</td><td> -</td><td> 1.6</td><td> 1.9</td><td></td>

<td> K2O</td><td> 3.3</td><td> 3.3</td><td> «</td><td></td><td> 3.2</td>

<td> CszO</td><td></td><td></td><td> 5.0</td><td> 3.7</td><td></td>

<td> RbsO</td><td></td><td></td><td> •</td><td></td><td></td>

<td> MgO</td><td></td><td></td><td> 3.9</td><td> 3.2</td><td> 0.2</td>

<td> CaO</td><td></td><td></td><td> .</td><td></td><td></td>

<td> SrO</td><td></td><td></td><td> -</td><td></td><td></td>

<td> ZnO</td><td> 8.7</td><td> 8.6</td><td> «</td><td></td><td> 8.3</td>

<td> AI2O3</td><td> 2.7</td><td> 2.7</td><td> 2.7</td><td> 2.7</td><td> 2.6</td>

<td> GazOa</td><td></td><td></td><td> -</td><td></td><td></td>

<td> LàzOa</td><td></td><td></td><td> .</td><td></td><td> .</td>

<td> ErzOa</td><td></td><td></td><td> 0.1</td><td> 0.1</td><td> .</td>

<td> ZrOz</td><td></td><td></td><td></td><td></td><td></td>

<td> SnOz</td><td></td><td></td><td> «</td><td></td><td></td>

<td> CeOz</td><td></td><td></td><td> 0.8</td><td> 1.5</td><td> .</td>

<td> GeOz</td><td></td><td></td><td> .</td><td></td><td> 89</td>

<td> MnOz</td><td></td><td></td><td> -</td><td></td><td></td>

<td> VzOs</td><td></td><td></td><td> 0.1</td><td> 0.1</td><td></td>

<td> TazOs</td><td></td><td></td><td> -</td><td></td><td></td>

<td> P2O5</td><td> 6.3</td><td> 5.0</td><td> 3.8</td><td> 3.7</td><td> 4.2</td>

<td> F</td><td></td><td></td><td> -</td><td></td><td></td>

<td> TbxO?</td><td></td><td></td><td> 0.3</td><td> 0.4</td><td></td>

<td> Tg/’C</td><td> 455</td><td> 459</td><td> 458</td><td> 463</td><td></td>

<td> Ts/’C, fe/min</td><td> 1500, 120</td><td> 1500, 120</td><td> 1500,120</td><td> 1500,120</td><td> 1400,120</td>

<td> TKb/’C, W min</td><td> 500,30</td><td> 500,30</td><td> 500,30</td><td> 500,30</td><td> 500,30</td>

<td> Tc/°C,tc/min</td><td> 840,30</td><td> 850,30</td><td> 800,30</td><td> 800,30</td><td> 820,30</td>

<td> Tpress / °C, ίρτθβδ / °C</td><td></td><td></td><td></td><td></td><td></td>

<td> Main crystal phase (wt-%)</td><td> UzSizOs,</td><td> LizSizOs,</td><td> LizSizOs,</td><td> LizSizOs, (33.6)</td><td> LizSizOs,</td>

<td> Further crystal phases (wt.-%)</td><td> Lew quartz, LisPOx</td><td> Low quartz, U3PO4</td><td> Low quartz, U3PO4, CsoeoaAISisOiz</td><td> Low quartz, (15.6) LiaPOx, (5.8) Cso.aoaAlSisOiz (10.0)</td><td> Low quartz, U3PO4</td>

<td> Ob.®/MPa</td><td> 458</td><td> 485</td><td> 516</td><td> 368</td><td></td>

<td> CR value</td><td> 90.90</td><td> 86.57</td><td> 73.4</td><td> 73.54</td><td></td>

<td> L*</td><td> 95.87</td><td> 95.52</td><td> 90.36</td><td> 82.05</td><td></td>

<td> a*</td><td> -0.24</td><td> -0.24</td><td> 0.32</td><td> 4.63</td><td></td>

<td> b*</td><td> 0.84</td><td> 0.66</td><td> 11.49</td><td> 26.02</td><td></td>

<td> CTE/1&amp;6K·’ (100500’C)</td><td></td><td></td><td></td><td></td><td></td>