Sio2 slurry for the production of quartz glass

197597/3 S1O2 slurry for the production of quartz glass as well as the application

of the slurry BACKGROUND

1. TECHNICAL FIELD 5 TThe present invention relates to the field of glass production, and more particularly, to a quarz slurry for producing quarz glass.

2. DISCUSSION OF RELATED ART

The quartz glass to be produced is present as a functional coating of a base body 10 (carrier), or in the form of an opaque or translucent quartz glass component, for instance a band- or plate-shaped quartz glass component A great number of different techniques are known for the production of plateshaped quartz glass components. For instance, US-PS 4,363,647 suggests that a planar layer of S1O2 soot should be continuously deposited by means of deposition 15 burners on a pre-sintered sand bed and vitrified by means of a ribbon burner while producing a quartz glass plate.

Crucible pulling methods for producing quartz glass plates are also known. However, the lateral dimensions of the plate are limited by the diameter of the crucible. This may lead to corrugations of the withdrawn quartz glass plate, and 20 the achievable dimensional stability is relatively poor. Moreover, the manufacture of opaque quartz glass plates in a melting method is not possible without taking special measures for producing or maintaining opacity in the molten state.

For some time components and layers consisting in part or entirely of opaque quartz glass have been used in applications as optical reflectors for generating a 25 diffuse reflection. These reflectors are distinguished by an adequately high degree of reflection at a very high temperature and thermal shock resistance. DE 10 2004 051 846 A1 describes the manufacture of such a reflector by means of a slurry method. In this process a highly filled, castable, aqueous slurry is prepared that contains amorphous S1O2 particles and is applied in the form of a slurry layer to a 30 base body of quartz glass. The amorphous S1O2 particles are produced by wet 1 197597/02 milling S1O2 granules and have a particle size in the range of not more than 500 pm, with S1O2 particles with particle sizes in the range between 1 pm and 50 pm accounting for the greatest volume fraction.

The solids content, the particle size and the particle size distribution of the S1O2 5 particles have impacts on the drying shrinkage of the slurry layer. For instance, drying shrinkage can be reduced by using rather coarse SiO2 particles. Together with a high solids content, SiO2 particles in the order of 1 pm and 50 pm show advantageous sintering properties and a comparatively low drying shrinkage. Therefore, the known slurry layer can be dried and vitrified without crack 10 formation, which is also due to interactions arising among the S1O2 particles in the aqueous phase of the slurry.

For the application of the slurry layer to the base body, spraying, electrostatically supported spraying, flow coating, spinning, immersion and dispersion coating are suggested. The slurry layer is subsequently dried and vitrified. 15 DE 103 19 300 A1 discloses a method for the production of a shaped silica glass body by electrophoretic deposition. A dispersion according to the type mentioned at the outset is here started from, the dispersion containing larger amorphous SiO2 particles with a D50 value between 1 pm and 200 pm and smaller amorphous SiO2 nanoparticles with a grain size in the range of 1 nm to 100 nm. The fraction of the 20 S1O2 nanoparticles is preferably between 1-10% by wt., with the larger amorphous S1O2 particles forming the remainder up to 100%. The filling degree of the dispersion is between 10% by wt. and 80% by wt., preferably between 50% by wt. and 70% by wt., and its viscosity is between 1 -1000 mPa s, preferably between 1 -100 mPas. 25 However, it has been found that the flow behavior of the known slurry is not optimal for some coating techniques. With a highly filled slurry according to DE 10 2004 051 846 A1, for instance, ..dressing11 or spreading by doctor blade of the slurry mass turns out to pose problems, and although the low-viscosity dispersion according to DE 103 19 300 A1 can be poured out easily, it flows off from the 30 coated surface immediately, so that only flat coating geometries are possible and small layer thicknesses are also only achievable, which in addition tend to form cracks during drying and sintering. 2 197597/02

Since the slurry technique as such would permit an inexpensive production of exact layers and whole quartz glass components, it would be desirable to eliminate said drawbacks.

5 BRIEF SUMMARY OOne aspect of the present invention provides a SiO2 slurry for the production of quartz glass, said SiO2 slurry comprising: a dispersion liquid and amorphous SiO2 particles with particle sizes up to a maximum of 500 pm, wherein a majority of the volume of the SiO2 slurry is composed of SiO2 particles with particles sizes in the 10 range of 1 pm to 60 pm, and SiO2 nanoparticles with particle sizes of less than 100 nm are present in the SiO2 slurry in a concentration in the range of 0.2% by wt. to 15% by wt. (of an entire solids content of the SiO2 slurry), wherein the SiO2 particles have a multimodal distribution of particle sizes with a first maximum of the size distribution in the range of 1 pm to 3 pm and a second maximum in the range 15 of 5 pm to 50 pm, and wherein the solids content (as a percentage by weight of the SiO2 particles and the SiO2 nanoparticles together) is in the range of 83% to 90%.

DETAILED DESCRIPTION 20 It is therefore the object of the present invention to prepare a slurry with a flow behavior that has been optimized with respect to processing by dressing or pouring of the slurry mass and with respect to drying and sintering without cracks.

Moreover, it is the object of the present invention to indicate a special use of the slurry according to the invention. 25 The present invention relates a SiO2 slurry for the production of quartz glass, with the slurry containing a dispersion liquid and amorphous SiO2 particles with particle sizes up to a maximum of 500 pm, wherein the largest volume fraction is composed of SiO2 particles with particles sizes in the range of 1 pm to 60 pm, as well as SiO2 nanoparticles with particle sizes of less than 100 nm in the range of 0.2% by wt. to 15% by wt. (of the entire 30 solids content).

Moreover, the present invention relates to a special use of the slurry. 3 197597/02

As for the slurry, said object starting from the slurry mentioned at the outset is achieved according to the invention in that the SiO2 particles have a multimodal particle size distribution with a first maximum of the size distribution in the range of 1 pm to 3 pm and a second maximum in the range of 5 pm to 50 pm, and that the 5 solids content (percentage by weight of the SiO2 particles and the SiO2 nanoparticles together) are in the range of 83 % to 90%

Typically, the above-mentioned highly filled and highly viscous slurry shows a dilatant-rheopexic behavior. This means that upon mechanical action (such as stirring, shaking, filling, dispersion coating, stripping, spreading by doctor blade) 10 the slurry exhibits increased viscosity (dilatancy) or that after mechanical impact the viscosity is increased for a short period of time (rheopexy). These closely related flow properties of the slurry shall be termed „rheopexy“ or „rheopexic“ in the following.

Thus the known slurry thickens under mechanical action. This flow behavior turns 15 out to be disadvantageous when a slurry layer is applied to and distributed over a surface by means of a tool, for instance during dispersion coating or stripping, troweling, dressing, scraping, filling, or the like. The known high-viscosity slurry is not well suited for these application techniques, which shall be summarized hereinafter under the term “spreading by doctor blade”, as it solidifies under the 20 action of the distributing force, thereby counteracting a uniform distribution. In the inactive condition it can become liquid again and then flow off from oblique surfaces. The photo of Fig. 2 shows the result of a doctor blade test using a slurry as described in DE 10 2004 051 846 A1.

It has been found that the flow behavior of such a slurry will change due to the 25 addition of a small amount of SiO2 nanoparticles towards a structurally viscous thixotropic behavior. „Thixotropy“ of the slurry manifests itself in that with a constant shear stress (for instance at a constant stirring rate) its viscosity is continuously decreasing for some time. Related therewith is “structural viscosity” in the case of which the 30 viscosity is also reduced due to shear, but which is not further decreasing at a constant shear stress. 4 197597/02

These closely related flow properties of the slurry shall be jointly termed as “thixotropy” or “thixotropic” in the following.

Due to its thixotropic flow behavior the slurry according to the invention will liquefy under shear stress. This property is conducive to a uniform outflow and to the 5 distribution of the slurry mass over a surface - also under the action of a force with a distributing effect.

The flow behavior of the slurry is above all defined by the solids content, namely in combination with and in dependence upon the content of S1O2 nanoparticles and the particle size distribution of the amorphous S1O2 particles. This shall be 10 explained in more detail hereinafter: • The solids content (percentage by weight of the S1O2 particles and the S1O2 nanoparticles together) of the slurry according to the invention is relatively high at a value ranging between 83% and 90%. Also without the addition of nanoparticles, the high solids content effects a high viscosity of the slurry, 15 thereby contributing to a uniform and low shrinkage of the slurry layer, so that cracks caused by drying and sintering are reduced. Very high solids contents of more than 90% reduce the further processing possibilities of the slurry even if it is mixed with S1O2 nanoparticles. • The addition of SiO2 nanoparticles creates interactions between the 20 amorphous S1O2 particles. The rather thixotropic behavior of the slurry according to the invention is due to diminishing interactions between the SiO2 particles upon occurrence of shear forces. After omission of the shear forces, in the passive state of the slurry mass, these interactions will augment again, leading to the formation of physical or chemical bonds 25 between the amorphous SiO2 particles of the slurry mass among one another, which stabilize the inactive slurry mass. • The amorphous SiO2 particles have a multimodal particle size distribution. Such a multimodal particle size distribution has at least two, preferably three or more, distribution maxima. This is conducive to the setting of a high 30 true density of the slurry, whereby shrinkage during drying and sintering and thus the risk of crack formation is reduced. For instance, particle 5 197597/02 distributions with D50 values of 2, 5,15, 30 and 40 pm can be used alone or in combination.

The S1O2 nanoparticles can e.g. be produced by oxidation or hydrolysis of silicon-containing starting compounds (also called “pyrogenic silica” in the following) or by 5 polycondensation of polymerizable silicon compounds (S1O2 sol). When “pyrogenic silica” is used, a previous cleaning step is often useful. For this purpose pyrogenic silica is preferably present in the form of a partly solidified, “temporary” S1O2 granulate, which permits the use of a standard hot chlorination method for cleaning purposes. During homogenization of the slurry the purified granulate 10 grains will again decompose into S1O2 nanoparticles due to the shear forces acting thereon.

The slurry can be easily adapted to the corresponding processing techniques by adapting the solids contents, the multimodal particle size distribution and the amount of S1O2 nanoparticles within the ranges indicated in claim 1. This shall be 15 explained in more detail hereinafter. Suitable processing techniques using such a slurry comprise spreading by doctor blade and pouring. As for the standard doctor blade techniques, a slightly higher content of SiO2 nanoparticles is more appropriate for slurries to be processed by pouring.

The photo of Fig. 1 shows the result of a doctor blade test using a slurry according 20 to the invention; it can just be seen as a uniform white area.

SiO2 nanoparticles are here understood to be S1O2 particles with particle sizes in the range of a few nanometers up to 100 nm. Such nanoparticles have a BET specific surface area of 40-800 m2/g, preferably between 55 m2/g and 200 m2/g.

At a content of less than 0.2% by wt. of said particles in the slurry the 25 nanoparticles do not have any significant impact on the flow behavior of the slurry, whereas contents of more than 15% by wt. lead to intensified shrinkage of the slurry during drying, which might aggravate a defect-free drying and sintering. With thin slurry layers a higher content of S1O2 nanoparticles can be used because thinner layers are less prone to shrinkage cracks than thicker layers. 6 197597/02

With respect to this it has turned out to be particularly advantageous when the slurry contains between 0.5 and 5 and particularly preferably between 1 and 3% by wt. of S1O2 nanoparticles (based on the entire solids content).

Preferably, the S1O2 nanoparticles have particle sizes of less than 50 nm. 5 Small SiO2 nanoparticles seal and consolidate the outer surface of the green body and thereby increase the green strength of the dried slurry as well as the sintering activity.

It has turned out to be particularly advantageous when at least 80% by wt., preferably at least 90% by wt., of the S1O2 particles are made spherical. 10 Spherical particles facilitate the setting of a high true density in the slurry, so that stresses are reduced during drying and sintering. Moreover, it has been found that spherical S1O2 particles in opaque quartz glass layers contribute to enhanced reflection, above all in the infrared range. Ideally, all S1O2 particles are made spherical. 15 In connection with a basically high content of spherical SiO2 particles it has, however, also turned out to be of advantage to some applications when the slurry contains finely divided, splintery S1O2 granules.

Due to the addition of finely divided, splintery S1O2 granules, which can be produced by milling, the mechanical strength of the green body is even further 20 enhanced after drying. The higher strength has a particularly positive effect in the case of thick slurry layers. The particle sizes of the finely divided, splintery SiO2 granules correspond approximately to those of the amorphous S1O2 particles and the weight fraction of splintery granules is 10% by wt. at the most (based on the total solids content). 25 Preferably, the SiO2 particles have a particle size distribution distinguished by a D50 value of less than 50 pm, preferably less than 40 pm. S1O2 particles in this order of magnitude exhibit an advantageous sintering behavior and a comparatively low drying shrinkage so that a corresponding slurry layer can be sintered and dried particularly easily without the formation of cracks. 30 This is due to interactions between the S1O2 particles that lead to the formation of 7 197597/02 molecular SiO2 bonds already in the slurry mass and therefore facilitate drying and sintering.

The dispersion liquid may be made up of an aqueous base. The polar nature of the aqueous phase of such a slurry may have an effect on the interaction of the 5 S1O2 particles. For the slurry according to the invention, however, a dispersion liquid is preferred that is based on an organic solvent, preferably on an alcoholic basis.

It has been found that a dispersion liquid of such a type makes it easy to keep a thixotropic flow behavior. Moreover, the drying process is much faster than in the 10 case of an aqueous slurry phase. This saves time and leads to a faster fixation of the slurry layer on a carrier, so that a flowing out on the edges is avoided. With the addition of a minor water amount (< 30% by vol.) in the dispersion liquid, the processing period can be adapted to the respective requirements.

It has turned out to be also advantageous, particularly with respect to a low affinity 15 to form cracks, when the solids content (percentage by weight of the SiO2 particles and the SiO2 nanoparticles together) is preferably at least 85% by wt.

Preferably, the SiO2 particles and the SiO2 nanoparticles consist of synthetic SiO2.

Synthetic SiO2 is distinguished by high purity. The slurry is therefore suited for forming opaque quartz glass of high purity. The quartz glass has an impurity 20 content of less than 1 wt. ppm, whereby it absorbs not much in the UV range up to 180 nm and is thus suited as a diffuse optical broadband reflector for use over a particularly wide wavelength range.

For the same reason the SiO2 content of the amorphous SiO2 particles is preferably at least 99.9% by wt. 25 The solids content of the slurry produced by using such particles consists of at least 99.9% by wt. of SiO2 (apart from the addition of dopant). Binders or other additives are normally not needed and are ideally not contained. The content of metal oxide impurities is preferably less than 1 wt. ppm. 8 197597/02

The cristobalite content in the dried SiO2 slurry should be not more than 0.1% by wt. at the most because, otherwise, sintering of the slurry layer may cause crystallization, which may lead to waste.

To enhance the etching resistance of the quartz glass made from the slurry it has 5 turned out to be useful when the slurry contains nitrogen, carbon or a chemical compound of these components that are incorporated into the quartz glass structure in the form of nitrides or carbides.

Nitrogen and/or carbon and/or one or more compounds of said components are added to the slurry. Nitrides or carbides effect a reinforcement of the quartz glass 10 structure and lead to improved resistance to etching. Suitable start substances, such as silazanes or siloxanes, are particularly evenly distributed in the slurry, from which a homogeneous doping of the quartz glass of the glass mass will result in the end.

As for the use, the above-mentioned object is achieved according to the invention 15 in that the SiO2 slurry according to the invention is used for producing a diffusely reflecting reflector of quartz glass. A diffusely reflecting reflector made from the slurry according to the invention is distinguished by a particularly high degree of reflection over a wide wavelength range. This is assumed to be due to the high solids content of the slurry and 20 particularly to the addition of SiO2 nanoparticles.

The diffusely reflecting reflector is present as an independent reflector component which is used in combination with an optical radiator, a heating element or for thermal shielding, or the reflector is formed as an opaque SiO2 layer on a carrier component. The reflector can e.g. be present in the form of a tube, bulb, a 25 compartment, bell, semi-shell, spherical or ellipsoidal segment, a plate, a heat shield, or the like.

In a first preferred alternative the diffusely reflecting reflector is used as a reflector layer of quartz glass on a carrier of quartz glass.

After drying and sintering of the slurry the reflector layer formed from the slurry 30 forms a coating on a carrier surface or a part thereof. The carrier of quartz glass substantially performs mechanical or chemical basic functions of the overall 9 197597/02 component, e.g. mechanical strength, thermal stability and chemical resistance, while the reflector layer considerably defines the optical properties. Typical layer thicknesses are in the range of 0.2 mm to 3 mm.

The reflector layer and the carrier are here made of the same material or at least 5 of similar materials, which has a particularly advantageous effect on the adhesion of the reflector layer to the carrier and on the thermal shock resistance of the overall component.

An alternative and equally preferred use of the slurry is characterized in that the diffusely reflecting reflector is formed as a carrier-less, preferably band- or plate- 10 shaped quartz glass component.

The use of a highly concentrated slurry according to the invention will prevent the formation of cracks caused by shrinkage. To be more specific, plate- or bandshaped quartz glass bodies are obtained that are distinguished by a homogeneous quartz glass layer of a predetermined thickness, which may be opaque or 15 transparent, depending on the corresponding sintering temperature and duration. Opaque plates are preferably obtained at sintering temperatures between 1200°C and 1350°C. These are particularly suited as diffusely reflecting reflector components. At higher sintering temperatures or with long sintering periods translucence or even transparence is achieved. 20 For obtaining a specific reflection behavior of the diffusely reflecting reflector it has turned out to be advantageous when a slurry is used that contains one or more dopants that generate optical absorption in quartz glass in the ultraviolet, visible or infrared spectral range.

The slurry is preferably used for producing a diffusely reflecting reflector for diffuse 25 reflection in the UV wavelength range below 240 nm. A high reflection in the UV wavelength range (e.g. of more than 90%) down to wavelengths around 180 nm presupposes opacity and ultrahigh purity of the quartz glass. Purity is e.g. guaranteed through the use of synthetically produced S1O2, where particularly a low degree of impurity with lithium oxide should be 30 noted. The content of lithium is below 100 wt. ppb, preferably at less than 20 wt. PPb. 10 197597/02

The invention shall now be explained in more detail with reference to embodiments and a drawing, in which:

Figure 1 shows a photograph illustrating the result of a doctor blade test using a slurry according to the invention;

Figure 2 shows a photograph which illustrates the result of a doctor blade test using a slurry according to the prior art;

Figure 3 shows a diagram of the SiO2 particle size distribution of a raw material component for use in a slurry according to the invention (prior to the addition of SiO2 nanoparticles); and 10

Figure 4 shows a micrograph of the SiO2 particle size distribution of the raw material component of Fig. 3. 1. Preparation of a SiO2 slurry

Figure 3 shows a particle size distribution of a raw material component. This is a 15 multimodal particle size distribution with a relatively narrow maximum of the size distribution at about 30 pm (D50 value) and with a secondary maximum in the range around 2 pm. This raw material component with a D50 value at 30 pm shall be called R30 hereinafter.

Figure 4 shows the particle size distribution as a SEM micrograph. It can be seen 20 that the individual SiO2 particles are made round and spherical.

For the preparation of the slurry other raw material components are used that have a D5o value at 5 pm, 15 pm and 40 pm, and the particle size distributions of which are otherwise similar to the ones shown in Figs. 3 and 4. Depending on their D50 value, these raw material components are designated as R5, R15, and as R4o, 25 respectively. Each of the raw material components are first cleaned in a hot chlorination process at a temperature in the range between 600°C and 1200°C.

Moreover, SiO2 nanoparticles with diameters of around 40 nm are used in the form of «pyrogenic silica", or in the form of a SiO2 sol. The pyrogenic silica is here present as a partly solidified “temporary” SiO2 granulate that is pre-treated by 30 sintering at a low temperature in the range of 600°C to 900°C and partly 11 197597/02 consolidated in this process. For setting a high purity the pre-treatment is carried out in a chlorine-containing atmosphere. On account of the small primary particle sizes of the granulates the comparatively low temperature during hot chlorination is sufficient. During homogenization of the suspension the granulate grains 5 decompose again into SiO2 nanoparticles due to the shear forces acting on them The following recipes have turned out to be useful:

Recipe 1 R30 500 g R15 200 g 10 R5 200g

Pyrogenic silica: 135 g with BET surface area of 50 m2/g.

The said components are dispersed in pure ethanol, yielding a solids content of 85% by wt.

The highly filled slurry prepared in this way shows a thixotropic behavior. The 15 slurries are therefore “spreadable” and that is why they are suited for processing techniques such as doctor blade processes. In each recipe the grain sizes below 60 pm account for the greatest volume fraction of the granules.

The slurry which is exclusively produced with synthetically produced spherical SiO2 particles of high purity is free of cristobalite and is distinguished by a low 20 impurity content of less than 1 wt. ppm.

Figure 1 shows the result of a doctor blade test using the slurry according to recipe 1. The layer produced thereby is continuous and exhibits a uniform layer thickness so that the photo just shows a homogeneous white area. By contrast, the photo of Figure 2 shows an irregular mass distribution with clots, as issues 25 from spreading by doctor blade of a rheopexic SiO2 slurry according to the prior art. A similar result is obtained when the pyrogenic silica is omitted in recipe 1. 2. Preparation of quartz glass using the slurry according to the invention

Example 1: preparation of diffusely reflecting surface areas on a carrier 12 197597/02 A spreadable S1O2 slurry according to the invention is used, wherein the slurry layer is produced by means of a dressing tool acting on a supply mass of the slurry in a metering and distributing manner.

The supply mass is either accumulated on the surface of the carrier, or it is 5 contained in a reservoir from which it can pass to the carrier surface. Under the mechanical distributing action of the dressing tool and in combination with the thixotropic properties of the slurry according to the invention the viscosity is reduced, which facilitates outflow and propagation of the slurry on the surface of the carrier. This is conducive to the formation of a uniform homogeneous layer of a 10 predetermined thickness.

The dressing tool, which performs a relative movement with respect to the carrier surface, is for instance a doctor blade tool, such as a horizontally rotating rod, a roll, a shaping tool, or the like. It is essential that the dressing tool is spaced apart from the surface of the carrier at a distance correlating with the thickness of the 15 layer to be formed.

Preferably, the slurry supply mass is present on a gap formed between the dressing tool and the carrier, which is movable by relative movement between dressing tool and carrier along the carrier. The distance between dressing tool and carrier forms a gap on which the slurry supply mass to be distributed is positioned 20 and the width of which corresponds to the thickness of the slurry layer to be formed.

As a rule, a constant layer thickness is desired. As a result, the gap has a width that is predetermined by a mechanical guide element along which the carrier or the dressing tool is guided for performing its relative movement. The carrier itself 25 can here also be used as the guide element.

The relative movement of dressing tool and carrier is here carried out with the help of a mechanical guide element which, on the one hand, coordinates the relative movement and which, on the other hand, predetermines the gap between carrier and dressing tool directly or indirectly. As a result, when the relative movement is 30 carried out, a constant gap width can be upheld in an easy way. This may e.g. be a guide rail along which the dressing tool moves across the carrier. The gap width 13 197597/02 is directly set by the thickness of the guide rail or indirectly by a stripper connected to the dressing tool.

The slurry supply mass is preferably contained in a reservoir which is arranged on the dressing tool and fluidically connected to the gap. The slurry supply mass 5 passes continuously from the reservoir via the gap to the surface of the carrier.

The reservoir is part of the dressing tool and ensures that slurry mass is always present on the gap across the whole gap width. With a movable dressing tool the reservoir is also moved with the dressing tool.

As a rule, the gap has a shape adapted to a coating surface of the carrier. This is 10 particularly useful in the case of an elongated carrier, the coating surface of which is not flat, but comprises, for instance, curved or obliquely extending areas extending in longitudinal direction. The shape of the dressing tool is here adapted to the surface profile of the carrier and it is thereby ensured that the gap width, viewed in a direction transverse to the direction of relative movement, is constant. 15 In the embodiment the slurry according to recipe 2 is used for producing a reflector layer on a cladding tube for an IR radiator in the form of a so-called „twin tube" made of quartz glass.

The twin tube consists of a cladding tube which is formed as an eight when viewed in cross section and is made of quartz glass, the tube being subdivided by a 20 central web into two compartments, each serving to accommodate a heating coil. On the upper side of the cladding tube that is oriented away from the main propagation direction a reflector layer shall be formed in the form of an opaque coating of S1O2 for diffuse reflection. The production thereof shall be explained hereinafter. 25 The surface of the twin tube is cleaned with alcohol and then in 3% hydrofluoric acid for eliminating other surface impurities, particularly alkali and alkaline earth compounds. The twin tube is then inserted into a doctor blade device. Said device consists of an elongated carrier for supporting the twin tube, a guide rail and a dressing tool with integrated slurry reservoir which is displaceable on the guide rail 30 along the twin tube. The dressing tool comprises a stripper with a bottom side profiled in such a way that it maintains a drawing gap of a constant width of 2 mm 14 197597/02 relative to the upper side of the twin tube. The reservoir is fluidically connected to the drawing gap and, viewed in the direction of displacement of the dressing tool, arranged in front thereof. Areas of the upper side of the twin tube that are not to be coated are covered with a sheet. The slurry is filled into the reservoir and the 5 dressing tool is drawn off swiftly and uniformly via the guide rail along the twin tube. A shear force that due to the thixotropic flow property of the slurry leads to a decrease in viscosity so that the slurry is distributed between twin tube and stripper and exits in a uniform way and at a constant thickness out of the drawing gap is here acting on the slurry in the area of the drawing gap. The viscosity of the 10 slurry applied to and resting on the coating surface increases again due to thixoptropy immediately after application, so that the coating does not deliquesce, but mainly maintains its form. The cover sheets are removed. A substantially constant layer thickness of the slurry layer of about 1 mm is thereby achieved.

Despite the curved surface of the twin tube, the use of the doctor blade device and 15 of the thixotropic slurry according to the invention permits a uniform coating of the surface with slurry layer, thereby ensuring, after drying and sintering, the formation of an optically homogeneous and esthetically appealing opaque reflector layer with a thickness of 0.8 mm. Due to its high purity the layer also reflects in the ultraviolet wavelength range below 200 nm. The opaque reflector layer is also suited for use 20 at elevated temperatures of more than 1000°C.

The reflectivity of the opaque reflector layer shall now be explained in more detail with reference to the reflection curve of Fig. 5.

Figure 5 shows the reflection behavior of the diffuse reflector produced according to Example 1 in the form of an opaque layer of opaque SiO2 layer in the 25 wavelength range of 250 nm to 3000 nm. The degree of reflection “R” in % based on the reflectivity of “Spectralon” is plotted on the y-axis and the wavelength □ of the operating radiation in nm on the x-axis. The reflectivity is determined by means of an Ulbricht sphere.

The curve shows the reflection progress in the case of an opaque layer of opaque 30 SiO2 with a thickness of 0.8 mm, with the sintering process being carried out in a sintering furnace at 1280°C (3h) in air. As can be seen therefrom, the SiO2 opaque 15 197597/02 layer of undoped S1O2 shows an approximately uniform degree of reflection R of around 95% in the wavelength range between about 300 nm and 2100 nm. The degree of reflection at 210 nm is here still higher than 98%. This high reflection in the VUV range permits the use of components coated in this way, for instance in 5 the UV disinfection sector.

Example 2: production of a quartz glass plate A homogeneous slurry is prepared with the help of recipe 3. The slurry is used for producing a quartz glass plate in a doctor blade process. A slurry layer with a thickness of 5 mm is here produced on a carrier. This is only possible on account 10 of the thixotropic flow behavior of the slurry.

After drying of the layer, which on account of the high solids content and the alcoholic base of the dispersion liquid is carried out within a few hours, the layer is sintered. Depending on sintering temperature and duration, a thin plate of transparent or opaque quartz glass is obtained. 16