The invention relates to a multi-component glass, a process for its preparation and its use.
Two groups of materials which have a low or even negative thermal expansion coefficient are known. These materials are employed for uses where the highest geometric precision is required including during variations in temperature, such as, for example, large lightweight reflecting telescopes (J. Spangenberg-Jolly, Zero Expansion Glass for Telescope Mirror Blanks. Ceram. Bull. 69 (1990) 1922-1924,
Glass ceramic systems form the first group.
Components of glass ceramics are produced by shaping from the glass melt. The composition of the glass melt is such that during subsequent tempering of the shaped body a controlled crystallization occurs above the transformation temperature of the glass. Crystalline phases with a negative thermal expansion coefficient, which compensate the positive thermal expansion coefficient of the remaining glass matrix, are formed during this. Known examples are glass ceramics from Schott Glas in Mainz, which are marketed under the name Ceran® or Zerodur® and have been employed for years for hot-plates and telescope mirrors.
Li—Al silicate ceramics, which have a similar composition to the glass ceramics and also have a negative thermal expansion coefficient, can also be prepared from powders via a sintering process (S. L. Swartz, Ceramics having negative coefficient of thermal expansion, method of making such ceramics, and parts made from such ceramics, U.S. Pat. No. 6,066,585, Patent, Emerson Electric Co., 2000).
Two-component glasses form the second group (zero expansion glasses, ZEG).
The ULE® glasses from Corning (USA), which, in addition to SiO2, comprise approx. 7 wt. % TiO2, have already been known for a long time
At higher TiO2 contents the thermal expansion coefficient of these (single-phase) glasses even becomes negative, the risk of crystallization increasing significantly with an increasing TiO2 content.
It is furthermore known that by fluorine doping of silica glass the expansion coefficient can be lowered from 0.5×10−6/K to 0.1×10−6/K
Another example is the significant reduction in the expansion coefficient of a borate glass by addition of CeO2
Only few multi-component glasses based on TiO2 and SiO2 are known, such as, for example, K2O—SiO2—TiO2 glass
The thermal expansion coefficient increases significantly in both compositions.
The ZEG glasses have the disadvantage, compared with glass ceramic, that the passing of the thermal expansion through zero cannot be adjusted by the composition. In the case of the Corning ULE glasses, which are prepared via gas phase deposition
It was not possible to reduce variations in refractive index of 4×10−5 by sol-gel processes
It is furthermore to be noted that thermal pretreatment has a significant influence on the properties of ULE glasses
The invention provides a multi-component glass, which is characterized in that, in addition to the components TiO2 and SiO2, it comprises a further component from the group consisting of glass-forming agents and/or intermediate oxides.
Glass-forming agents can be oxides such as, for example, B2O3. Intermediate oxides can be oxides such as, for example, CeO2.
The problems of the prior art mentioned are solved according to the invention in that at least one further network-forming glass component which at most slightly increases and primarily even further decreases the thermal expansion is added to the TiO2—SiO2 glass. The third or all further components furthermore have the effect that the stability of the TiO2 in the silicate glass matrix is improved, without substantially influencing the chemical properties.
This third component can be:
Network-forming polyvalent cations, such as B2O3, have proved to be particularly advantageous, it being possible for the glass to comprise 70-90 wt. % SiO2, 1-10 wt. % TiO2 and 0.1-7 wt. % B2O3.
The components furthermore can be distributed so homogeneously that no nucleation takes place and crystallization of individual components is therefore suppressed.
There are two process for preparation of the glass composition according to the invention:
The solutions can be, for example, aqueous salt solutions or reactive alkoxide solutions in an alcohol, preferably ethanol. The latter can react, after introduction into the pores, and form oxide powder particles of the desired composition of the additional components homogeneously distributed in the pores in respect of the chemical composition.
The suspension can comprise very fine particles with diameters which are smaller than the average pore size of the green bodies to be impregnated.
It has proved advantageous to distribute the dispersed particles homogeneously in the open pore volumes of the green bodies by application of electrical fields (electrophoretic impregnation, EPI).
For this, the green body must have been filled beforehand with a low-conducting liquid, so that the dispersed particles of the suspension can move from a storage reservoir into the green body.
In both process variants shaped bodies with a geometry close to the final dimensions are produced, for example by pouring into a mould.
The dispersing liquid or the liquid phase formed during the reaction is then removed, after which the green body is formed.
The green body is then sintered to give a dense shaped body, the process temperature when nanopowders are used being significantly below the melting temperature of ULE glasses.
The considerable advantages of the multi-component glasses according to the invention are their improved glass stability and a lower sintering temperature.
Furthermore, by the shaping processes of powder technology shaped bodies with dimensions close to the final dimensions can be produced directly at room temperature, which avoids the high finishing costs of the glass ceramics and ULE glasses.
An example of the thermal expansion of a glass which has the composition according to the invention and is prepared via the sintering process (impregnation process) is shown in
Number | Date | Country | Kind |
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10319596.3 | May 2003 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP04/04096 | 4/17/2004 | WO | 8/25/2006 |