Glass compositions
4 claims: 4 independent, 0 dependent
- 1Process for producing an IR and UV absorbing soda-lime-silica glass containing oxides of iron and cobalt and having a ferrous iron to total iron (as Fe2O3) ratio in the range of 21 to 34, including admixing, heating and melting a soda-lime-silica float glass batch mixture comprising sand, soda ash, dolomite, limestone, and a sulfate selected from the group consisting of salt cake and gypsum, and including in said batch wuestite as at least a partial source of the iron oxides in the resulting glass. Procédé de production d'un verre de silicate sodocalcique absorbant les IR et les UV, contenant des oxydes de fer et de cobalt ayant une rapport fer ferreux/fer total (en Fe2O3) dans la gamme de 21 à 34, qui consiste à mélanger, chauffer et faire fondre une composition de verre flotté de silicate sodocalcique comprenant du sable, du carbonate de sodium, de la dolomite, du calcaire, et un sulfate choisi dans le groupe constitué par le gâteau de sel et le gypse, et contenant, dans ladite composition, de la wuestite en tant que source au moins partielle des oxydes de fer dans le verre résultant. Verfahren zum Herstellen eines IR und UV absorbierenden Natronkalk-Kiesel-Glases, das Eisenoxid und Kobalt enthält und ein Verhältnis Eisen II zu Gesamteisen (als Fe2O3) im Bereich von 21 zu 34 aufweist, bei dem eine Natronkalk-Kiesel-Floatglaschargenmischung gemischt, aufgeheizt und geschmolzen wird, die Sand, wasserfreies Soda, Dolomit, Kalkstein und Sulfate, ausgewählt aus der Gruppe bestehend aus Natriumsulfatkuchen und Gips, enthält und die in der Charge Wüstit als mindestens eine Teilquelle der Eisenoxide in dem resultierenden Glas enthält.
- 2Process according to claim 1 preparing a base glass composition by admixing in percent by weight:SiO265 - 80Na2O10 - 20CaO5 - 15MgO0 - 10Al2O30 - 5K2O0 - 5BaO0 - 5B2O30 - 5 and traces of melting and refining aids, if any. Procédé selon la revendication 1 de préparation d'une composition de verre de base par mélange, en pourcentage pondéral, de: SiO265 - 80%Na2O10 - 20CaO5 - 15MgO0 - 10Al2O30- 5K2O0 - 5BaO0-5B2O30-5 et de traces d'auxiliaires de fusion et d'affinage éventuels. Verfahren nach Anspruch 1 zum Herstellen eines Basisglasgemischs durch Mischen in Gewichtsprozenten von: SiO265 - 80Na2O10 - 20CaO5 - 15MgO0 - 10Al2O30 - 5K2O0 - 5BaO0 - 5B2O30 - 5 und gegebenenfalls von Spuren von Schmelz- und Läuterungshilfsmitteln.
- 3Process according to claim 1 or 2 including adding in percent by weight as essential ingredients a total iron content expressed as Fe2O3 from 0,3% to 0,7%, from 0,5 to 10 ppm Se, from 3 to 25 ppm Co3O4, 0 to 50 ppm NiO and 0 to 1,5% TiO2. Procédé selon la revendication 1 ou 2, comprenant l'addition, en tant qu'ingrédients essentiels, en pourcentage pondéral, d'une teneur totale en fer, exprimée en Fe2O3, de 0,3% à 0,7%, de 0,5 à 10 ppm de Se, de 3 à 25 ppm de Co3O4, de 0 à 50 ppm de NiO et de 0 à 1,5% de TiO2. Verfahren nach Anspruch 1 oder Anspruch 2, das das Hinzufügen, in Gewichtsprozenten eines Gesamteisengehaltes, ausgedrückt als Fe2O3 von 0,3% bis 0,7%, 0,5 bis 10 ppm Se, 3 bis 25 ppm Co3O4, 0 bis 50 ppm NiO und 0 bis 1,5% TiO2 als wesentliche Bestandteile enthält.
- 4Process according to one of claims 1 to 3 including adding in percent by weight as essential ingredients a total iron content expressed as Fe2O3 from 0,45% to 0,65%, from 1 to 5 ppm Se, from 8 to 20 ppm Co3O4, 0 to 35 ppm NiO and 0 to 1% TiO2, and having a ferrous iron to total iron (as Fe2O3) ratio in the range of 25 to 31. Procédé selon l'une quelconque des revendications 1 à 3, comprenant l'addition, en tant qu'ingrédients essentiels, en pourcentage pondéral, d'une teneur totale en fer, exprimée en Fe2O3, de 0,45% à 0,65%, de 1 à 5 ppm de Se, de 8 à 20 ppm de Co3O4, de 0 à 35 ppm de NiO et de 0 à 1% de TiO2, et ayant un rapport du fer ferreux au fer total (en Fe2O3) dans la gamme de 25 à 31. Verfahren nach einem der Ansprüche 1 bis 3, das das Hinzufügen, in Gewichtsprozenten, eines als Fe2O3 ausgedrückten Gesamteisengehaltes von 0,45% bis 0,65%, 1 bis 5 ppm Se, 8 bis 20 ppm Co3O4, 0 bis 35 ppm NiO und 0 bis 1% TiO2 als wesentliche Bestandteile enthält und wobei ein Eisen II zu Gesamteisen (als Fe2O3) Verhältnis im Bereich von 25 bis 31 vorhanden ist.
Independent claims4
26 paragraphs in 3 sections, as filed
BACKGROUND OF THE INVENTION
The present invention relates to infrared (IR) and ultraviolet (UV) absorbing soda-lime-silica glass compositions for use in glazing. More particularly, the present invention relates to windows of a neutral tint made from such glasses primarily, but not exclusively, for vehicles such as automobiles.
Special glasses have been developed for use in vehicles which have low levels of direct solar heat transmission (DSHT) and ultraviolet transmission (UVT). These glasses aim to reduce the problems caused by excessive heating within the vehicle on sunny days, and to protect the interior furnishings of the car from the degradation caused by ultraviolet radiation. Glasses having good infrared absorption properties are usually produced by reducing iron present in the glass to the ferrous state or by adding copper. Such materials give glasses a blue color. The materials added to achieve good ultraviolet radiation absorption are Fe<sup>3+</sup>, Ce, Ti or V. The quantities of such materials which are added to provide the desired level of absorption tend to color the glass yellow. Accordingly, if both good UV and good IR absorption are required in the same glass, the color of such glass is, almost inevitably, either green or blue. When the color of the glasses is defined by the CIELAB system, such commercial glasses, in 4 mm thickness and having greater than 60% light transmission, are found to be either very green (-a*>8) or very blue (-b*>7), neither of which are currently desirable from an aesthetic viewpoint.
Attempts have been made to produce grey or bronze-colored vehicle glazing having good protection against both IR and UV radiation, but such glasses still tend to have a greenish yellow tinge.
We have identified a requirement for a range of glasses having a neutral tint and a visible light transmittance (Illuminant A) of at least 70 percent such that, in the CIELAB system, the glasses have color co-ordinates lying in the ranges a<sup>*</sup> from -7 to +1, b<sup>*</sup> from -5 to +7.5. The term "neutral tint" is hereinafter used to describe glasses having such color co-ordinates.
We have further identified a requirement for glasses having a neutral tint which have visible light transmissions of at least 70 percent (at a thickness of 4 mm), but which also have a direct solar heat transmission which is at least twelve percentage points (preferably fifteen percentage points and most preferably twenty percentage points) less than the visible light transmission. Basically, glasses are known which do have a low direct solar heat transmission but nearly all of these have a low visible light transmission which tend to make such glasses of limited use in vehicles. Glasses satisfying the above-identified requirements should, we anticipated, be of more general use in vehicles due to the higher light transmission but the lower direct solar heat transmission should keep the interior of the car cool despite the higher light transmission.
Furthermore, we believed that it would be desirable if the glasses had an ultraviolet transmission less than 55% and ideally less than 50% because we felt that such a low transmission would minimize the adverse effects of ultraviolet radiation on plastics material and fabrics, particularly in automotive vehicles.
The field of tinted glasses is one in which relatively small changes can produce major changes in tint. Wide ranges disclosed in prior patents can encompass many possibilities, and it is only the teaching of the specific examples that can be relied on as identifying how particular tints associates with particular ranges of absorption of infrared and ultraviolet radiation can be obtained.
Our invention includes the surprising discovery that the incorporation of relatively small amounts of certain coloring agents compensates for the green color arising from the presence of infrared and ultraviolet radiation absorbing components.
FR 2 690 437 and US 5 318 931 describe windows for vehicles, the glass composition containing in percentage by weight 65 - 80% SiO<sub>2</sub>, 0 - 5% Al<sub>2</sub>O<sub>3</sub>, 0 - 5% B<sub>2</sub>O<sub>3</sub>, 0 - 10% MgO, 5 - 15% CaO, 10 - 18% Na<sub>2</sub>O, 0 - 5% K<sub>2</sub>O, 5 - 15% of MgO and CaO, 10 - 20% in total of Na<sub>2</sub>O and K<sub>2</sub>O, 0,3 - 2% cerium oxide in terms of CeO<sub>2</sub>, 0 - 1% TiO<sub>2</sub>, 0,1 - 0,8% iron oxide in terms of Fe<sub>2</sub>O<sub>3</sub>, 0 - 0,006% CoO, 0 - 0,01T NiO and 0 - 0,0015% Se.
SUMMARY OF THE INVENTION
According to the present invention, there is provided a process for producing an IR and UV absorbing soda lime silica glass containing oxides of iron and cobalt and having a ferrous iron to total iron (as Fe<sub>2</sub>O<sub>3</sub>) ration in the range of 21 to 34, including admixing, heating and melting a soda-lime-silica float glass batch mixture comprising sand, soda ash, dolomite, limestone, and a sulfate selected from the group consisting of salt cake and gypsum, and including in said batch wuestite as at least a partial source of the iron oxides in the resulting glass.
The produced soda lime silica glass has a neutral tint (as herein defined) and, in a 4 mm thickness, a visible light transmission of at least 70%, a direct solar heat transmission at least 12 percentage points below the visible light transmission, a UV transmission not greater than 55%, a dominant wavelength less than 560 nm and a color purity not greater than 6, preferably not more than 5 and most preferably no more than 3. Most, preferably the direct solar heat transmission is at least 20 percentage points lower than the visible light transmission. The composition comprises a soda-lime-silica base glass and a total iron content, expressed as Fe<sub>2</sub>O<sub>3</sub>, in the range of from 0.3 to 0.7% by weight. The glass is tinted to a neutral color by the inclusion of 0.5 to 10 parts by million (ppm) of Se, from about 3 to 25 ppm of Co<sub>3</sub>O<sub>4</sub>, and a ferrous iron content to provide a ratio of ferrous iron to total iron in the range of 21 to 34, preferably 25 to 31 (i.e., percent of total iron as ferrous iron (Fe<sup>2+</sup>) of 21% to 34%, preferably 25% to 31%*). NiO and TiO<sub>2</sub> may be added to the glass, in ranges of 0 to 50 ppm NiO and 0 to 1.5 weight percent TiO<sub>2</sub>. Thus, it has been determined that amounts of NiO and TiO<sub>2</sub>, in the above ranges can produce beneficial affects on color purity and UV absorption, respectively, without deleteriously influencing the unique and highly advantageous properties of our novel glass. * As is well known, the iron content in glasses is usually present in both the Fe<sub>2</sub>O<sub>3</sub> (ferric) and FeO (ferrous) forms. As is conventional, the total amount of iron present in a glass is expressed herein as Fe<sub>2</sub>O<sub>3</sub>, regardless of the form actually present.
For the purpose of the present specification, references to visible light transmission are to light transmission (LT) measured using CIE Illuminant A; UVT or ultraviolet radiation transmission is an integrated term representing the area under the transmission versus wavelength curve for wavelengths between 300 and 400 nm; and references to direct solar heat transmission (DSHT) are references to solar heat transmission integrated over the wavelength range 350 to 2100 nm according to the relative solar spectral distribution Parry Moon for air mass 2.
Suitable batch materials for producing glasses according to the present invention, which materials are compounded by conventional glass batch ingredient mixing devices, include sand, limestone, dolomite, soda ash, salt cake or gypsum, niter, iron oxide, carbon, selenium and cobalt oxide (Co<sub>3</sub>O<sub>4</sub>). In the event TiO<sub>2</sub> and/or NiO are desired in the composition, a titanium compound such as titanium dioxide and a nickel compound such as nickel oxide may be included in the batch. In this connection, and in accordance with an important embodiment of this invention it has surprisingly been discovered that the use of wuestite as the source of iron is particularly advantageous, supplying at least a partial amount or preferably all of the Fe<sub>2</sub>O<sub>3</sub> and substantially eliminating the need for carbon. Thus, carbon is a very deleterious element in neutral tint glasses, e.g., grey and bronze glasses, but is required to raise the ferrous values of the glasses where employing rouge as the batch iron source. The use of wuestite as the iron source instead of rouge greatly increases the ferrous value of a glass. The use of a raw material with a higher natural ferrous value allows better control of higher ferrous values in glasses such as the neutral tint glasses of this invention.
The batch materials are conveniently melted together in a conventional glass making furnace, to form a neutral tinted infrared energy and ultraviolet radiation absorbing glass composition, which thereafter may be continuously cast onto the molten metal bath in a float glass process.
The composition of soda-lime-silica flat glasses suitable for use in accordance with the present invention typically have the following weight percentage constituents: <tables id="tabl0001" num="0001"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">SiO<sub>2</sub></entry><entry namest="col2" nameend="col2" align="center">65-80%</entry></row><row><entry namest="col1" nameend="col1" align="left">Na<sub>2</sub>O</entry><entry namest="col2" nameend="col2" align="center">10-20</entry></row><row><entry namest="col1" nameend="col1" align="left">CaO</entry><entry namest="col2" nameend="col2" align="center">5-15</entry></row><row><entry namest="col1" nameend="col1" align="left">MgO</entry><entry namest="col2" nameend="col2" align="center">0-10</entry></row><row><entry namest="col1" nameend="col1" align="left">Al<sub>2</sub>O<sub>3</sub></entry><entry namest="col2" nameend="col2" align="center">0-5</entry></row><row><entry namest="col1" nameend="col1" align="left">K<sub>2</sub>O</entry><entry namest="col2" nameend="col2" align="center">0-5</entry></row><row><entry namest="col1" nameend="col1" align="left">BaO</entry><entry namest="col2" nameend="col2" align="center">0-5</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">B<sub>2</sub>O<sub>3</sub></entry><entry namest="col2" nameend="col2" align="center">0-5</entry></row></tbody></tgroup></table></tables>
Other minor ingredients, including melting and refining aids such as SO<sub>3</sub>, may also appear in the glass composition. The coloring constituents of the present invention set forth above are added to this base glass. The glass is essentially free of colorants other than iron, cobalt, and selenium, and optionally nickel and titanium, other than any trace amounts of oxides that may be present as impurities. Accordingly, the glass produced according to the present invention may be melted and refined in a conventional tank-type melting furnace and formed into flat glass sheets of varying thicknesses by the float method in which the molten glass is supported on a pool of molten metal, usually tin, as it assumes a ribbon shape and is cooled.
The glass compositions are particularly suited for the production of infrared energy and ultraviolet radiation absorbing glass for automotive and architectural glazings. Thus, glass sheets of this composition may be heat strengthened or tempered, or alternately annealed and laminated together through an interposed transparent resinous layer, for example composed of polyvinyl butyral, and employed, for example, as a windshield. Generally, the glass sheets for windshield use are of a thickness in the range of from about 1.7 mm to about 2.5 mm, while those tempered and used as sidelights or backlights are in the range of about 3 mm to about 5 mm thick.
Unless otherwise noted, the term percent (%) as used herein and in the appended claims, means percent (%) by weight. Wavelength dispersive X-ray fluorescence was used to determine the weight percents, of TiO<sub>2</sub> and total iron expressed as Fe<sub>2</sub>O<sub>3</sub>. Percent reduction of total iron was determined by first measuring the radiant transmission of a sample at a wavelength of 1060 nanometers, using a spectrophotometer. The 1060 nm transmission value was then used to calculate optical density, using the following formula:<maths id="math0001" num=""><math display="block"><mrow><msub><mrow><mtext>Optical density = Log</mtext></mrow><mrow><mtext>10</mtext></mrow></msub><mtext></mtext><mfrac><mrow><msub><mrow><mtext>T</mtext></mrow><mrow><mtext>o</mtext></mrow></msub></mrow><mrow><mtext>T</mtext></mrow></mfrac></mrow></math><img file="EP0721429B1_D0001.tif" /></maths> (T<sub>o</sub> = 100 minus estimated loss from reflection=92; T = transmission at 1060 nm). The optical density was then used to calculate the percent reduction:<maths id="math0002" num=""><math display="block"><mrow><mtext>percent reduction = </mtext><mfrac><mrow><mtext>(110)x(optical density) </mtext></mrow><mrow><msub><mrow><mtext>(Glass thickness in mm)x(wt% total Fe</mtext></mrow><mrow><mtext>2</mtext></mrow></msub><msub><mrow><mtext>O</mtext></mrow><mrow><mtext>3</mtext></mrow></msub><mtext>)</mtext></mrow></mfrac></mrow></math><img file="EP0721429B1_D0002.tif" /></maths>
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
The concentrations of each of the three essential colorant constituents depend upon the optical properties desired for the glass and are interrelated to each other. Iron is added, typically as Fe<sub>2</sub>O<sub>3</sub>, and is partially reduced to FeO. The total amount of iron in the batch is critical, and must equal from 0.3 percent to about 0.7 percent by weight, expressed as Fe<sub>2</sub>O<sub>3</sub>. Likewise, the degree of reduction is critical and must equal between 21% and 34%. If the iron is more highly reduced than the critical amount, or if a higher total amount of iron is employed, the glass will become too dark and the Illuminant A visible light transmittance will drop below about 70 percent. Additionally, the glass batch melting process will become increasingly difficult as the increased amount of FeO prevents the penetration of heat to the interior of the melt. If the iron is less reduced than the critical amount, or if a lower total amount of iron is employed, then the direct solar heat transmittance for a desired thickness glass can rise to an unacceptable level, i.e., above about 58%.
From about 3 to about 25 ppm cobalt oxide is added, typically as Co<sub>3</sub>O<sub>4</sub>, along with about 0.5 to about 10 ppm selenium. The proper selenium and cobalt content provides an aesthetically pleasing, neutral tint, somewhat gray color to the glass. Preferred compositions, include a soda-lime-silica base glass and colorants consisting essentially of 0.45 to 0.65 total iron (as Fe<sub>2</sub>O<sub>3</sub>), with a ratio of ferrous iron to total iron of 25 to 31, 1 to 5 ppm Se, 8 to 20 ppm Co<sub>3</sub>O<sub>4</sub>, 0 to 35 ppm NiO and 0 to 1 weight percent TiO<sub>2</sub>.
The following examples illustrate glass compositions produced in accordance with the invention that are readily formed into glass articles or glazings such as automobile windshields. The compositions absorb both infrared and ultraviolet rays and have an Illuminant A visible light transmission of at least about 70% and a direct solar heat transmission at least 12 percentage points less than the visible light transmission.
The examples, except examples 1 and 11 which are for comparison purposes only, are produced according to the invention. In the examples, all parts and percentages are by weight and: <ul id="ul0001" list-style="none" compact="compact"><li>(a) Fe<sub>2</sub>O<sub>3</sub>, FeO, and TiO<sub>2</sub> are expressed in percent; Se, Co<sub>3</sub>O<sub>4</sub> and NiO are expressed in parts per million;</li><li>(b) total iron is expressed as if all iron present were present as ferric oxide; and</li><li>(c) the FeO content is calculated from the equation<maths id="math0003" num=""><math display="block"><mrow><mtext>%FeO = </mtext><mfrac><mrow><msup><mrow><mtext>%Fe</mtext></mrow><mrow><mtext>2+</mtext></mrow></msup></mrow><mrow><mtext>100</mtext></mrow></mfrac><msub><mrow><mtext> x Fe</mtext></mrow><mrow><mtext>2</mtext></mrow></msub><msub><mrow><mtext>O</mtext></mrow><mrow><mtext>3</mtext></mrow></msub><mtext> x </mtext><mfrac><mrow><mtext>143.7</mtext></mrow><mrow><mtext>159.7</mtext></mrow></mfrac></mrow></math><img file="EP0721429B1_D0003.tif" /></maths> Fe<sub>2</sub>O<sub>3</sub>=percentage total iron, expressed as Fe<sub>2</sub>O<sub>3</sub>, in the glass (143.7 being the molecular weight of 2 x FeO and 159.7 being the molecular weight of Fe<sub>2</sub>O<sub>3</sub>).</li></ul>
The transmittance data in the Table below and throughout are based on a nominal glass thickness of 4mm. <tables id="tabl0002" num="0002"><img file="EP0721429B1_D0004.tif" /></tables><tables id="tabl0003" num="0003"><img file="EP0721429B1_D0005.tif" /></tables>
The base glass composition for example 7, which is essentially the same for all of the examples, was as follows: <tables id="tabl0004" num="0004"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Component</entry><entry namest="col2" nameend="col2" align="center">Weight Percent of Total Glass</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">SiO<sub>2</sub></entry><entry namest="col2" nameend="col2" align="char" char=".">73.91</entry></row><row><entry namest="col1" nameend="col1" align="left">Na<sub>2</sub>O</entry><entry namest="col2" nameend="col2" align="char" char=".">14.04</entry></row><row><entry namest="col1" nameend="col1" align="left">CaO</entry><entry namest="col2" nameend="col2" align="char" char=".">7.86</entry></row><row><entry namest="col1" nameend="col1" align="left">MgO</entry><entry namest="col2" nameend="col2" align="char" char=".">3.47</entry></row><row><entry namest="col1" nameend="col1" align="left">SO<sub>3</sub></entry><entry namest="col2" nameend="col2" align="char" char=".">0.20</entry></row><row><entry namest="col1" nameend="col1" align="left">Al<sub>2</sub>O<sub>3</sub></entry><entry namest="col2" nameend="col2" align="char" char=".">0.16</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">K<sub>2</sub>O</entry><entry namest="col2" nameend="col2" align="char" char=".">0.039</entry></row></tbody></tgroup></table></tables> The batch mixture for example 7, which is likewise similar for all of the examples except for the colorants, was: <tables id="tabl0005" num="0005"><table frame="all"><tgroup cols="2" colsep="1" rowsep="0"><colspec colnum="1" colname="col1" colwidth="78.75mm" /><colspec colnum="2" colname="col2" colwidth="78.75mm" /><thead valign="top"><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Constituent</entry><entry namest="col2" nameend="col2" align="center">Parts by Weight</entry></row></thead><tbody valign="top"><row><entry namest="col1" nameend="col1" align="left">Sand</entry><entry namest="col2" nameend="col2" align="center">154</entry></row><row><entry namest="col1" nameend="col1" align="left">Soda Ash</entry><entry namest="col2" nameend="col2" align="center">50</entry></row><row><entry namest="col1" nameend="col1" align="left">Gypsum</entry><entry namest="col2" nameend="col2" align="center">1</entry></row><row><entry namest="col1" nameend="col1" align="left">Limestone</entry><entry namest="col2" nameend="col2" align="center">11</entry></row><row><entry namest="col1" nameend="col1" align="left">Dolomite</entry><entry namest="col2" nameend="col2" align="center">33</entry></row><row><entry namest="col1" nameend="col1" align="left">Wuestite</entry><entry namest="col2" nameend="col2" align="center">1.02</entry></row><row><entry namest="col1" nameend="col1" align="left">Co<sub>3</sub>O<sub>4</sub></entry><entry namest="col2" nameend="col2" align="center">0.0011</entry></row><row><entry namest="col1" nameend="col1" align="left">Selehium</entry><entry namest="col2" nameend="col2" align="center">0.0014</entry></row><row rowsep="1"><entry namest="col1" nameend="col1" align="left">Carbon</entry><entry namest="col2" nameend="col2" align="center">0.027</entry></row></tbody></tgroup></table></tables>
It is an advantage of the present invention that the composition can be manufactured into flat glass products using commercial manufacturing processes, in particular the float process. A sheet of glass that has been formed by the float process is characterized by measurable amounts of tin oxide that migrated into surface portions of the glass on at least one side. Typically a piece of float-forming glass has an SnO<sub>2</sub> concentration of at least 0.05% by weight in the first few microns below the surface that was in contact with the tin. Glass made by the float process typically ranges from about 2 millimeters to 10 millimeters in thickness.
Another characteristic of most float glass is the presence of traces of melting and refining aids such as sulfur, analyzed in the glass as SO<sub>3</sub>, or fluorine or chlorine. Small amounts of these melting and refining aids (usually less than 0.3% by weight) may be present in the glass compositions of the present invention without effect on the properties.
Contents3
5 sheets
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70 members in 24 offices
Priority claims7
| Document | Office | Kind | Date |
|---|---|---|---|
| 285652 | United States of America | – | |
| 28565294 | United States of America | A | |
| 9509149 | United States of America | W | |
| 285652 | – | – | – |
| US19940285652 | – | – | – |
| US9509149 | – | – | – |
| WO1995US09149 | – | – | – |
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| RU2118616C1 | Russian Federation | C1 | |
| ES2119169T3 | Spain | T3 | |
| DE69411543T2 | Germany | T2 | |
| AU699949B2 | Australia | B2 | |
| AU9046798A | Australia | A | |
| DK0682646T3 | Denmark | T3 | |
| US5910460A | United States of America | A | |
| US5928974A | United States of America | A | |
| CN1044357C | China | C | |
| TW367312B | Taiwan Province of China | B | |
| AU715351B2 | Australia | B2 | |
| PL178725B1 | Poland | B1 | |
| IN184251B | India | B | |
| EP1067098A1 | European Patent Office (EPO) | A1 | |
| EP0721429B1This record | European Patent Office (EPO) | B1 | |
| DE69520871D1 | Germany | D1 | |
| CN1073052C | China | C | |
| DE69520871T2 | Germany | T2 | |
| JP3253086B2 | Japan | B2 | |
| US2002025899A1 | United States of America | A1 | |
| KR100322760B1 | Republic of Korea | B1 | |
| KR100360628B1 | Republic of Korea | B1 | |
| EP1067098B1 | European Patent Office (EPO) | B1 | |
| DE69530330D1 | Germany | D1 | |
| CZ292624B6 | Czechia | B6 | |
| ES2194674T3 | Spain | T3 | |
| DE69530330T2 | Germany | T2 | |
| DE69411543T4 | Germany | T4 | |
| JP2005047801A | Japan | A | |
| JP3731896B2 | Japan | B2 | |
| US6998362B2 | United States of America | B2 | |
| JP3769571B2 | Japan | B2 | |
| CA2154279C | Canada | C | |
| CA2172133C | Canada | C |
27 legal events, as 2 offices reported them to INPADOC
Over the term
Point at a mark for the eventEvents
| Event | Code | Office | |
|---|---|---|---|
| Notification of lapseLapsedST | ST | FR | |
| No opposition filedOpposition26N | 26N | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Gb: european patent ceased through non-payment of renewal feeCeasedGBPC | GBPC | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| No opposition filed within time limitOppositionORIGINAL CODE: 0009261PLBE | PLBE | EP | |
| Information on the status of an ep patent application or granted ep patentGrantedSTATUS: NO OPPOSITION FILED WITHIN TIME LIMITSTAA | STAA | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Fr: translation filedET | ET | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Corresponds to:REF | REF | EP | |
| Designated contracting statesAK | AK | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| Lapsed in a contracting state [announced via postgrant information from national office to epo]LapsedPG25 | PG25 | EP | |
| (expected) grantORIGINAL CODE: 0009210GRAA | GRAA | EP | |
| Despatch of communication of intention to grant a patentORIGINAL CODE: EPIDOS IGRAGRAH | GRAH | EP | |
| Despatch of communication of intention to grantORIGINAL CODE: EPIDOS AGRAGRAG | GRAG | EP | |
| Despatch of communication of intention to grant a patentORIGINAL CODE: EPIDOS IGRAGRAH | GRAH | EP | |
| Despatch of communication of intention to grantORIGINAL CODE: EPIDOS AGRAGRAG | GRAG | EP | |
| Despatch of communication of intention to grantORIGINAL CODE: EPIDOS AGRAGRAG | GRAG | EP | |
| First examination report despatched17Q | 17Q | EP | |
| Supplementary search report drawn up and despatchedA4 | A4 | EP | |
| Designated contracting statesAK | AK | EP | |
| Request for examination filed17P | 17P | EP | |
| Designated contracting statesAK | AK | EP | |
| Public reference made under article 153(3) epc to a published international application that has entered the european phaseORIGINAL CODE: 0009012PUAI | PUAI | EP |
Numbers
- Publication
- 0721429
- Publication, DOCDB
- 0721429
- Publication, EPODOC
- EP0721429
- Application
- 95927301
- Application, DOCDB
- 95927301
- Application, EPODOC
- EP19950927301
Titles3
- German
- GLASZUSAMMENSETZUNGEN
- English
- GLASS COMPOSITIONS
- French
- COMPOSITIONS DE VERRE
Classification
- CPC, 6
- C03C1/00
- C03C1/10
- C03C3/087
- C03C4/02
- C03C4/082
- C03C4/085
- IPC, 7
- C03C1 00
- C03C1 10
- C03C3 087
- C03C4 02
- C03C4 08
- C03C6 00
- C03C6 04
Designated states7
- Contracting states, 7
- Belgium
- Germany
- Spain
- France
- United Kingdom
- Italy
- Luxembourg
