WO2005068393A1 - Fusion-cast refractory with high electrical resistivity - Google Patents

Fusion-cast refractory with high electrical resistivity Download PDF

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Publication number
WO2005068393A1
WO2005068393A1 PCT/US2004/044042 US2004044042W WO2005068393A1 WO 2005068393 A1 WO2005068393 A1 WO 2005068393A1 US 2004044042 W US2004044042 W US 2004044042W WO 2005068393 A1 WO2005068393 A1 WO 2005068393A1
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Prior art keywords
refractory
cao
fusion
electrical resistivity
content
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PCT/US2004/044042
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French (fr)
Inventor
Amul Gupta
Dr. Steven M. Winder
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Vesuvius Crucible Company
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Application filed by Vesuvius Crucible Company filed Critical Vesuvius Crucible Company
Priority to AT04816024T priority Critical patent/ATE510804T1/en
Priority to AU2004313955A priority patent/AU2004313955B2/en
Priority to US10/585,165 priority patent/US7598195B2/en
Priority to EP04816024A priority patent/EP1711445B1/en
Priority to JP2006547592A priority patent/JP4714697B2/en
Priority to CN200480039608XA priority patent/CN1902142B/en
Priority to BRPI0418269A priority patent/BRPI0418269B1/en
Publication of WO2005068393A1 publication Critical patent/WO2005068393A1/en
Priority to ZA2006/05017A priority patent/ZA200605017B/en

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    • C04B35/484Refractories by fusion casting
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Definitions

  • the present invention relates to fusion-cast zirconia materials, and in particular, to a fusion-cast zirconia refractory having high electrical resistivity suitable for use in glass-melting furnaces.
  • Fused refractories comprising primarily Zr0 2 (“zirconia”) are traditionally used in glass melting furnaces.
  • the zirconia provides excellent corrosion resistance to the molten glass.
  • Refractories utilizing AI 2 0 3 -Zr ⁇ 2 -Si0 2 known as AZS refractories are well known in the art. Such refractories that have a Zr0 2 concentration of 80 wt % or higher are referred to as high- zirconia fused refractories.
  • the refractory used in the glass melting furnace have high electrical resistivity. It is also generally desirable that the refractory provides superior resistance to corrosion and thermal cycling.
  • the '643 Patent discloses a fused zirconia refractory that utilizes 0.05 to 1.0% of P 2 0 5 in order to soften the matrix glass. Though this refractory exhibits an acceptable level of electrical resistance, its main objective was to improve the thermal cycling resistance and it does so by increasing the total amount of the glassy phase, which may decrease the corrosion resistance of the refractory.
  • the '612 Patent discloses a fused zirconia refractory that eliminates the use of P 2 0 5 , but adds in 0.05 to 3% of BaO, SrO and MgO in total, in order to reduce the stresses on the glassy phase of the refractory that are caused by the elimination of P 2 0 5 .
  • the '612 Patent further discloses the use of Na 2 0 (in an amount greater than .05%) and K 2 0 to reduce the tensile stress that is caused by the addition of the alkaline earth metal oxides listed above. The presence of
  • the present invention seeks to achieve high electrical resistance in the fused
  • Zirconia refractory while minimizing the concentration of BaO, SrO, MgO, CaO, P 2 0 5 , Na 2 0 and
  • a fusion-cast refractory comprises 0.8% to 2.5% Al 2 0 3 , 4.0% to 10.0% Si0 2 , 86% to 95% Zr0 2 , 0.1% to 1.2% B 2 0 3 , up to 0.04% Na 2 0, up to 0.4% CaO, up to 0.1 % Fe 2 0 3 and up to 0.25% Ti0 2 .
  • the refractory comprises 0.8% to 2.5% Al 2 0 3 , 4.0% to 10.0% Si0 2 , 86% to 95% Zr0 2 , 0.1% to 1.2% B 2 0 3 , up to 0.04% Na 2 0, up to 0.4% CaO, up to 0.1 % Fe 2 0 3 and up to 0.25% Ti0 2 .
  • the present invention is a fusion-cast refractory comprising 0.8% to 2.5% Al 2 0 3 , 4.0% to 10.0% Si0 2l 86% to 95% Zr0 2 , 0.1% to 1.2% B 2 0 3 , up to 0.04% Na 2 0, up to 0.4% CaO, up to 0.1% Fe 2 0 3 and up to 0.25% Ti0 2 .
  • Refractories made in accordance with the present invention are characterized by an electrical resistivity of at least 80 ohm-cm at 1625°C.
  • the present invention is a fusion-cast refractory comprising 0.9% to 2.0% Al 2 0 3 , 6.0% to 8.0% Si0 2 , 88% to 92% Zr0 2 , 0.3% to 0.9% B 2 0 3 , up to 0.04% Na 2 0, up to 0.2% CaO, up to 0.05% Fe 2 0 3 and up to 0.15% Ti0 2 .
  • the Zr0 2 content of the refractory according to the invention is 86 to 94%, and preferably is 88 to 94%.
  • the Si0 2 content of the refractory according to the invention is 4 to 10%, or preferably 6 to 8%.
  • the glass phase cannot be formed as a continuous matrix phase at a content of less than 4%, while poor resistance to molten glass may be expected at a content of higher than 10%.
  • the Al 2 0 3 content of the refractory according to the present invention is 0.8 to 2.5%, and preferably 0.9 to 2.0%. Al 2 0 3 improves the flowability of the melt at a content higher than 0.8%, but content higher than 2.5% leads to instability of the glass phase, rendering the product prone to failure.
  • the B 2 0 3 content of the refractory according to the present invention is 0.1 to 1.2%, and is preferably 0.3 to 0.9%.
  • the addition of B 2 0 3 aids in suppressing cracks in the refractory during fabrication. This benefit is not realized at a content of less than 0.1%, and concentrations over 1.2% can cause an anomalous behavior of the glassy phase.
  • CaO is an optional component of the refractory according to the present invention, and is present in an amount from 0.0 to 0.4% of the refractory.
  • the CaO may be added in order to help reduce the stresses in the refractory and to reduce cracking during fabrication.
  • the addition of CaO is also beneficial when the refractory of the present invention is used in a glass melting furnace where TFT-LCD glass or plasma display panels are formed, as those molten glasses may also contain CaO.
  • Na 2 0 and K 2 0 are also optional components of the refractory according to the present invention, present in an amount from 0.0 to 0.04% of the refractory.
  • the alkali is a preferably eliminated from the refractory, as it is the major source of electrical conduction in the glass.
  • Ti0 2 and Fe 2 0 3 may be present as impurities, but their individual concentrations should not exceed 0.25% for the Ti0 2 , 0.1% for the Fe 2 0 3 , and the total concentration should not exceed 0.35% because they may encourage defect forming potential of the refractory. Examples
  • the raw materials include zirconia (derived from zircon sand by removing most of its silica), zircon sand, calcined alumina, boric oxide, calcium carbonate, and dead-burned magnesia. These raw materials are selected such that the impurities (such as Fe 2 0 3 , Ti0 2 , Na 2 0, K 2 0) are reduced to a minimum level.
  • the raw materials were carefully weighed and blended into a homogeneous mixture, and subsequently discharged into a large steel crucible for melting.
  • the steel crucible was powered by graphite electrodes using 3 phase current supply.
  • the outside of crucible was cooled by water continuously during the operation.
  • the liquid in this container is allowed to cool rapidly.
  • the resulting sample is tested for chemistry using an X-ray Fluorescence Spectrometer. All but one constituents of the zirconia refractory can be analyzed quantitatively using the X-ray Fluorescence Spectrometer.
  • B 2 0 3 is analyzed using either Inductively Coupled Plasma Spectrometer (ICP) or DC Arc Emission method. The chemistries of the various samples are listed in the table below.
  • the density may be obtained from a small cylindrical core sample, about 25mm in diameter and 100mm long, using Archimedes Water Immersion method, or by weighing the complete casting (after it has been machined to remove the mold skin) and dividing the weight by the casting's external volume.
  • the electrical resistivity was measured on a cylindrical sample, 25mm in diameter and 50mm long, using a 4-point electrode assembly. The ends of the sample are coated with platinum ink. Platinum ink was also placed on the circumference of the sample at two places, 25 mm apart and 12.5 mm from each end. Platinum wire was then wrapped around under each end of the sample, as well as on the two internal places mentioned above. Current was applied along the ends and voltage drop is measured across the 25mm band in the guage section described above. Resistivity is measured both using alternating and direct current. [0024] The microstructure is checked on a series of samples, each about 25mm long by 15mm wide mounted in an epoxy resin and polished to 1 micron surface finish.
  • These samples can be taken from a cylindrical core, typtcally drilled on a perpendicular through the center of the broadest face of the block so as to represent the average microstructure. Polished sections are typically prepared from regions close to the outside face of the casting as well as its core The microstructure can be checked using both an Optical microscope and Electron Microscope. Identification of crystalline phases is done using an X-ray diffractometer. Glass phase chemistry can be defined using Energy Dispersive Spectrometry (EDS) in the electron microscope. Mean boron content of the glass phase can be estimated by difference of the total analysis from 100%. It can also be more accurately computed from data derived from bulk chemical analysis on powder obtained from the same sample - by ratio with the Silicon content determined by both EDS and bulk chemistry methods.
  • EDS Energy Dispersive Spectrometry
  • Resistance to thermal cycling is typically performed on samples, 25mm in diameter by 50mm long, taken from various locations in the casting
  • the samples are cycled from 1250C to 800C at least 20 times using a controlled heat-up and cool down rate in an electric furnace.
  • the change in sample volume can be measured using Water Immersion method.
  • the presence of cracks can be documented using a photograph.
  • Examples 4-13 were produced using the method described above Comparative Examples 1-3 were produced using the same method
  • the chemical makeup of each example is listed in the table below.
  • the electrical resistivity for each example is also provided in the table below.
  • examples 4, 12 and 13 provided the most desirable results. All of the examples 4-13 achieved the desired resistivity of at least 80 ohm-cm. All of the examples were also acceptable in terms of resistance to thermal cycling.

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Abstract

A fusion-cast refractory is provided. The refractory comprises 0.8% to 2.5% Al 2 O 3 , 4.0% to 10.0% SiO 2 86% to 95% ZrO 2 , 0.1% to 1.2% B 2 O 3 , up to 0.04% Na 2 O, up to 0.4% CaO, up to 0.1% Fe 2 O 3 and up to 0.25% TiO 2 ..

Description

Fusion-Cast Zirconia Refractory With High Electrical Resistivity.
Specification.
Cross-reference to related applications. [0001] This application claims the benefit under 35 U.S.C. §120 of the filing date of U.S.
Provisional Application No. 60/533,990 filed January 2, 2004.
Field of the invention.
[0002] The present invention relates to fusion-cast zirconia materials, and in particular, to a fusion-cast zirconia refractory having high electrical resistivity suitable for use in glass-melting furnaces.
Description of the related art.
[0003] Fused refractories comprising primarily Zr02 ("zirconia") are traditionally used in glass melting furnaces. The zirconia provides excellent corrosion resistance to the molten glass.
Refractories utilizing AI203-Zrθ2-Si02, known as AZS refractories are well known in the art. Such refractories that have a Zr02 concentration of 80 wt % or higher are referred to as high- zirconia fused refractories.
[0004] It is desirable, especially in the production of high-quality glasses, such as TFT-LCD glass and plasma display panels, that the refractory used in the glass melting furnace have high electrical resistivity. It is also generally desirable that the refractory provides superior resistance to corrosion and thermal cycling.
[0005] High-zirconia fused refractories have been disclosed, for example, in U.S. Patent Nos.
5,466,643 to Ishino, et al. (the "643 Patent") and 5,679,612 to Endo, et al. (the "612 Patent"), the entire contents of both of which are hereby incorporated by reference.
[0006] The '643 Patent discloses a fused zirconia refractory that utilizes 0.05 to 1.0% of P205 in order to soften the matrix glass. Though this refractory exhibits an acceptable level of electrical resistance, its main objective was to improve the thermal cycling resistance and it does so by increasing the total amount of the glassy phase, which may decrease the corrosion resistance of the refractory.
[0007] The '612 Patent discloses a fused zirconia refractory that eliminates the use of P205, but adds in 0.05 to 3% of BaO, SrO and MgO in total, in order to reduce the stresses on the glassy phase of the refractory that are caused by the elimination of P205. The '612 Patent further discloses the use of Na20 (in an amount greater than .05%) and K20 to reduce the tensile stress that is caused by the addition of the alkaline earth metal oxides listed above. The presence of
Na20 and K20, in dissimilar amounts, may not provide the most optimized electrical resistance in the refractory.
[0008] Therefore, the present invention seeks to achieve high electrical resistance in the fused
Zirconia refractory, while minimizing the concentration of BaO, SrO, MgO, CaO, P205, Na20 and
K20. Summary ofthe invention.
[0009] In order to achieve the listed objectives, a fusion-cast refractory is provided. The refractory comprises 0.8% to 2.5% Al203, 4.0% to 10.0% Si02, 86% to 95% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1 % Fe203 and up to 0.25% Ti02. Detailed description of the preferred embodiments.
[0010] Except where otherwise noted, all percentages listed below, including in any claims, are on a weight basis and are a percentage of the fusion-cast refractory as measured from the pourstream. The present invention is a fusion-cast refractory comprising 0.8% to 2.5% Al203, 4.0% to 10.0% Si02l 86% to 95% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1% Fe203 and up to 0.25% Ti02. Refractories made in accordance with the present invention are characterized by an electrical resistivity of at least 80 ohm-cm at 1625°C. It is recognized that refractories with lower Zr02 content and higher glass content can also be manufactured but that their utility is limited. [0011] In a preferred embodiment, the present invention is a fusion-cast refractory comprising 0.9% to 2.0% Al203, 6.0% to 8.0% Si02, 88% to 92% Zr02, 0.3% to 0.9% B203, up to 0.04% Na20, up to 0.2% CaO, up to 0.05% Fe203 and up to 0.15% Ti02. [0012] The Zr02 content of the refractory according to the invention is 86 to 94%, and preferably is 88 to 94%. Zr02 content higher than 94% does not offer crack-free refractories, while Zr02 content lower than 86% leads to poor resistance to molten glass. [0013] The Si02 content of the refractory according to the invention is 4 to 10%, or preferably 6 to 8%. The glass phase cannot be formed as a continuous matrix phase at a content of less than 4%, while poor resistance to molten glass may be expected at a content of higher than 10%. [0014] The Al203 content of the refractory according to the present invention is 0.8 to 2.5%, and preferably 0.9 to 2.0%. Al203 improves the flowability of the melt at a content higher than 0.8%, but content higher than 2.5% leads to instability of the glass phase, rendering the product prone to failure.
[0015] The B203 content of the refractory according to the present invention is 0.1 to 1.2%, and is preferably 0.3 to 0.9%. The addition of B203 aids in suppressing cracks in the refractory during fabrication. This benefit is not realized at a content of less than 0.1%, and concentrations over 1.2% can cause an anomalous behavior of the glassy phase.
[0016] CaO is an optional component of the refractory according to the present invention, and is present in an amount from 0.0 to 0.4% of the refractory. The CaO may be added in order to help reduce the stresses in the refractory and to reduce cracking during fabrication. The addition of CaO is also beneficial when the refractory of the present invention is used in a glass melting furnace where TFT-LCD glass or plasma display panels are formed, as those molten glasses may also contain CaO.
[0017] Na20 and K20 are also optional components of the refractory according to the present invention, present in an amount from 0.0 to 0.04% of the refractory. The alkali is a preferably eliminated from the refractory, as it is the major source of electrical conduction in the glass. [0018] Ti02 and Fe203 may be present as impurities, but their individual concentrations should not exceed 0.25% for the Ti02, 0.1% for the Fe203, and the total concentration should not exceed 0.35% because they may encourage defect forming potential of the refractory. Examples
[0019] The raw materials include zirconia (derived from zircon sand by removing most of its silica), zircon sand, calcined alumina, boric oxide, calcium carbonate, and dead-burned magnesia. These raw materials are selected such that the impurities (such as Fe203, Ti02, Na20, K20) are reduced to a minimum level. The raw materials were carefully weighed and blended into a homogeneous mixture, and subsequently discharged into a large steel crucible for melting. The steel crucible was powered by graphite electrodes using 3 phase current supply. The outside of crucible was cooled by water continuously during the operation. [0020] The raw materials were melted for one hour and the liquid was poured into a graphite mold. During normal production, this batch process is repeated every hour, 24 hours a day, and up to 7 days a week. The graphite mold was surrounded by calcined alumina powder in a large steel container (known as a bin). After the mold was filled completely, the top of the mold was covered with calcined alumina powder and the bin was stored inside the building for a period of at least 2 weeks to allow the casting to cool slowly. This is important to ensure that the casting is recovered with minimal to no cracking. [0021] While filling the mold, during pouring of the liquid from the crucible, a small sample of the liquid is collected in a graphite container. The liquid in this container is allowed to cool rapidly. The resulting sample is tested for chemistry using an X-ray Fluorescence Spectrometer. All but one constituents of the zirconia refractory can be analyzed quantitatively using the X-ray Fluorescence Spectrometer. B203 is analyzed using either Inductively Coupled Plasma Spectrometer (ICP) or DC Arc Emission method. The chemistries of the various samples are listed in the table below.
[0022] The density may be obtained from a small cylindrical core sample, about 25mm in diameter and 100mm long, using Archimedes Water Immersion method, or by weighing the complete casting (after it has been machined to remove the mold skin) and dividing the weight by the casting's external volume.
[0023] The electrical resistivity was measured on a cylindrical sample, 25mm in diameter and 50mm long, using a 4-point electrode assembly. The ends of the sample are coated with platinum ink. Platinum ink was also placed on the circumference of the sample at two places, 25 mm apart and 12.5 mm from each end. Platinum wire was then wrapped around under each end of the sample, as well as on the two internal places mentioned above. Current was applied along the ends and voltage drop is measured across the 25mm band in the guage section described above. Resistivity is measured both using alternating and direct current. [0024] The microstructure is checked on a series of samples, each about 25mm long by 15mm wide mounted in an epoxy resin and polished to 1 micron surface finish. These samples can be taken from a cylindrical core, typtcally drilled on a perpendicular through the center of the broadest face of the block so as to represent the average microstructure. Polished sections are typically prepared from regions close to the outside face of the casting as well as its core The microstructure can be checked using both an Optical microscope and Electron Microscope. Identification of crystalline phases is done using an X-ray diffractometer. Glass phase chemistry can be defined using Energy Dispersive Spectrometry (EDS) in the electron microscope. Mean boron content of the glass phase can be estimated by difference of the total analysis from 100%. It can also be more accurately computed from data derived from bulk chemical analysis on powder obtained from the same sample - by ratio with the Silicon content determined by both EDS and bulk chemistry methods.
[0025] Resistance to thermal cycling is typically performed on samples, 25mm in diameter by 50mm long, taken from various locations in the casting The samples are cycled from 1250C to 800C at least 20 times using a controlled heat-up and cool down rate in an electric furnace. Following this test, the change in sample volume can be measured using Water Immersion method. Also, the presence of cracks can be documented using a photograph.
[0026] Examples 4-13 were produced using the method described above Comparative Examples 1-3 were produced using the same method The chemical makeup of each example is listed in the table below. The electrical resistivity for each example is also provided in the table below.
Chemistry ( t%) 1 2 3 4 5 6 7 8 9 10 11 12 13 A1203 1 06 1 1 11 1 05 0 95 0 89 0 9 1 85 1 61 1 39 1 12 0 96 1 09 Siθ2 4- 76 4 36 5 27 6 63 5 81 6 07 5 82 7 91 7 3 7 06 6 94 7 18 8 77 Fe2θ3 0 03 0 03 0 03 0 035 0 03 0 03 0 04 0 04 0 03 0 03 0 03 0 03 0 07 Ti02 0 1 0 10 0 10 0 11 0 11 0 12 0 12 0 13 0 14 0 13 0 13 0 07 0 08 Na20 0 033 0 018 0 03 0 012 0 024 0 022 0 02 0 020 0 017 0 030 0 005 0 0 CaO 0 31 0 37 0 29 0 047 0 09 0 179 0 19 0 06 0 057 0 06 0 11 0 05 0 08 MgO 02 0 19 0 2 0 0 023 0 05 0 06 0 0 0 0 0 0 B2θ3 0 27 0 3 0 43 0 88 0 3 0 27 0 28 0 64 0 84 0 86 0 78 0 68 0 58 Zr02 93 2 93 6 92 5 91 2 92 7 924 92 6 89 4 90 0 90 4 90 9 91 0 89 3 Bulk Density (g/cc) 5 31 5 21 5 36 5 21 5 36 5 36 5 39 5 24 5 22 5 26 5 32 5 09 4 98
DC Resistivity (ohm-cm) at 1625C 38 55 58 133 104 90 94 98 87 88 101 257 332
[0027] As can be seen, from the standpoint of electrical resistivity, examples 4, 12 and 13 provided the most desirable results. All of the examples 4-13 achieved the desired resistivity of at least 80 ohm-cm. All of the examples were also acceptable in terms of resistance to thermal cycling.
[0028] Obviously, numerous modifications and variations of the present invention are possible It is, therefore, to be understood that within the scope of the following claims, the invention may be practiced otherwise than as specifically described.

Claims

Claims.
We claim:
I . A refractory comprising 0.9% to 2.5% Al203, 4.0% to 10.0% Si02, 86% to 95% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1% Fe03 and up to 0.25% Ti02. 2. The refractory of claim 1 , comprising 0.9% to 2.0% Al203, 4.0% to 10.0% Si02, 86% to
95% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1% Fe03 and up to 0.25% Ti02.
3. The refractory of claim 2, comprising 0.95% to 1.85% Al203, 4.0% to 10.0% Si02, 86% to 95% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1% Fe03 and up to 0.25% TiO2.
4. The refractory of claims 1 to 3, comprising 0.9% to 2.5% Al203, 4.4% to 8.8% Si02, 86% to 95% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1 % Fe03 and up to 0.25% Ti02.
5. The refractory of claim 4, comprising 0.9% to 2.5% Al203, 6% to 8% Si02, 86% to 95% Zr02, 0.1 % to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1 % Fe03 and up to
0.25% Ti02.
6. The refractory of claims 1 to 5, comprising 0.9% to 2.5% Al203, 4.4% to 8.8% Si02, 88% to 95% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1% Fe03 and up to 0.25% Ti02. 7. The refractory of claim 6, comprising 0.9% to 2.5% Al203, 4.0% to 10.0% Si02, 89.3% to
93.6% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1% Fe03 and up to 0.25% Ti02.
8. The refractory of claims 1 to 7, comprising 0.9% to 2.5% Al203, 4.0% to 10.0% Si02, 86% to 95% Zr02, 0.3% to 0.9% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1% Fe03 and up to 0.25% Ti02.
9. The refractory of claims 1 to 8, consisting essentially of 0.9% to 2.5% Al203, 4.0% to 10.0% Si02, 86% to 95% Zr02, 0.1% to 1.2% B203, up to 0.4% CaO, up to 0.1% Fe03 and up to 0.25% Ti02.
10. The refractory of claims 1 to 8, consisting essentially of 0.9% to 2.5% Al203, 4.0% to 10.0% Si02, 86% to 95% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.1% Fe03 and up to 0.25% Ti02.
I I . The refractory of claims 1 to 8, consisting essentially of 0.9% to 2.5% Al203, 4.0% to 10.0% Si02, 86% to 95% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO and up to 0.25% Ti02. 12. The refractory of claims 1 to 8, consisting essentially of 0.9% to 2.5% Al203, 4.0% to
10.0% Si02, 86% to 95% Zr02, 0.1% to 1.2% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1% Fe03 and up to 0.25% TiOz.
13. The refractory of claim 1 , consisting essentially of 0.95% to 1.85% Al203, 4.4% to 8.8% Si02, 89.3% to 93.6% Zr02, 0.3% to 0.9% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1% Fe03 and up to 0.25% Ti02.
14. The refractory of claim 1 , wherein the refractory has an electrical resistance of at least 80 ohm-cm at 1625°C.
15. The refractory of claim 1 , wherein the refractory has an electrical resistance of at least 100 ohm-cm at 1625°C. 16. The refractory of claim 1 , wherein the refractory has an electrical resistance of at least 130 ohm-cm at 1625°C.
17. The refractory of claim 1 , wherein the refractory has an electrical resistance of at least 250 ohm-cm at 1625°C.
18. The refractory of claim 1 , wherein the refractory has an electrical resistance of at least 300 ohm-cm at 1625°C.
19. A refractory comprising 0.95% to 1.85% Al203, 4.4% to 8.8% Si02, 89.3% to 93.6% Zr02, 0.3% to 0.9% B203, up to 0.04% Na20, up to 0.4% CaO, up to 0.1% Fe03 and up to 0.25% Ti02.
20. The refractory of claim 19, consisting essentially of 0.96% to 1.1 % Al203, 6.6% to 8.8% Si02, 89.3% to 91.2% Zr02, 0.6% to 0.9% B203, up to 0.02% Na20, up to 0.1% CaO, up to 0.1%
FeO3 and up to 0.1% TiO2.
21. The refractory of claim 20, consisting essentially of 0.96% to 1.1% Al203, 6.6% to 8.8% Si02, 89.3% to 91.2% Zr02, 0.6% to 0.9% B203, up to 0.1% CaO, up to 0.1% Fe03 and up to 0.1% TiO2. 22. The refractory of claim 19, wherein the refractory has an electrical resistance of at least 80 ohm-cm at 1625°C.
23. The refractory of claim 19, wherein the refractory has an electrical resistance of at least 100 ohm-cm at 1625°C.
24. The refractory of claim 19, wherein the refractory has an electrical resistance of at least 130 ohm-cm at 1625°C.
25. The refractory of claim 19, wherein the refractory has an electrical resistance of at least 250 ohm-cm at 1625°C.
26. The refractory of claim 21 , wherein the refractory has an electrical resistance of at least 300 ohm-cm at 1625"C.
PCT/US2004/044042 2004-01-02 2004-12-30 Fusion-cast refractory with high electrical resistivity WO2005068393A1 (en)

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AT04816024T ATE510804T1 (en) 2004-01-02 2004-12-30 FELTS-CAST REFRIGERANT MATERIALS BASED ON ZIRCONIUM OXIDE WITH HIGH ELECTRICAL RESISTANCE
AU2004313955A AU2004313955B2 (en) 2004-01-02 2004-12-30 Fusion-cast refractory with high electrical resistivity
US10/585,165 US7598195B2 (en) 2004-01-02 2004-12-30 Fusion-cast refractory with high electrical resistivity
EP04816024A EP1711445B1 (en) 2004-01-02 2004-12-30 Fusion - cast zirconia refractory with high electrical resistivity
JP2006547592A JP4714697B2 (en) 2004-01-02 2004-12-30 Melt cast zirconia refractory with high electrical resistance
CN200480039608XA CN1902142B (en) 2004-01-02 2004-12-30 Fusion-cast refractory with high electrical resistivity
BRPI0418269A BRPI0418269B1 (en) 2004-01-02 2004-12-30 refractory
ZA2006/05017A ZA200605017B (en) 2004-01-02 2006-06-19 Fusion-cast refractory with high electrical resistivity

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WO2011092656A1 (en) 2010-01-28 2011-08-04 Saint-Gobain Centre De Recherches Et D'etudes Europeen Refractory product having a high zirconia content
US8796167B2 (en) 2010-01-28 2014-08-05 Saint-Gobain Centre De Recherches Et D'etudes Europeen Refractory product having high zirconia content
US8822362B2 (en) 2010-01-28 2014-09-02 Saint-Gobain Centre De Recherches Et D'etudes Europeen Refractory product having high zirconia content
US8859445B2 (en) 2010-01-28 2014-10-14 Saint-Gobain Centre De Recherches Et D'etudes Europeen Refractory product having high zirconia content
WO2011092657A1 (en) 2010-01-28 2011-08-04 Saint-Gobain Centre De Recherches Et D'etudes Europeen Refractory product having high zirconia content
JP2016000690A (en) * 2010-01-28 2016-01-07 サン−ゴバン サントル ド レシェルシュ エ デテュド ユーロペアン Refractory product having high zirconia content
WO2011092658A1 (en) 2010-01-28 2011-08-04 Saint-Gobain Centre De Recherches Et D'etudes Europeen Refractory product having high zirconia content
WO2016125317A1 (en) 2015-02-02 2016-08-11 Saint-Gobain Tm K.K. High zirconia electrically fused cast refractory
KR20160146798A (en) 2015-02-02 2016-12-21 산고반.티에무 가부시키가이샤 High zirconia electrically fused cast refractory
US9751806B2 (en) 2015-02-02 2017-09-05 Saint-Gobain Tm K.K. High zirconia electrically fused cast refractory

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AU2004313955A1 (en) 2005-07-28
ZA200605017B (en) 2008-01-08
AU2004313955B2 (en) 2009-09-10
EP1711445B1 (en) 2011-05-25
CN1902142B (en) 2010-12-22
US7598195B2 (en) 2009-10-06
EP1711445A1 (en) 2006-10-18
JP4714697B2 (en) 2011-06-29
EP1711445A4 (en) 2008-12-03
BRPI0418269B1 (en) 2016-03-08
JP2007517754A (en) 2007-07-05
BRPI0418269A (en) 2007-05-02
US20070249481A1 (en) 2007-10-25
CN1902142A (en) 2007-01-24
ATE510804T1 (en) 2011-06-15
RU2006124609A (en) 2008-01-20

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