CROSS-REFERENCE TO RELATED APPLICATION 0001 This application claims the benefit of U.S. Provisional Application No. 60/170,286, filed Dec. 10, 1999, entitled METHODS OF INCREASING THE REDOX RATIO OF IRON IN A GLASS ARTICLE, which is herein incorporated by reference.

BACKGROUND OF THE INVENTION 0002 The present invention relates generally to iron-containing glass articles and glass compositions and, more particularly, to a method of increasing the redox ratio of iron in glass articles and glass compositions. 0003 In conventional float glass production operation, a batch of glass forming components is heated in a furnace to melt the glass forming components into a liquid mass. Furnaces for glass batch melting include conventional furnaces that employ chemical refining and overhead heating or other special glass melting furnaces, such as vacuum or physical refining furnaces. The melted batch components react to produce a glass which is then removed from the furnace and deposited onto a pool of molten tin. The glass is formed, processed and cooled to form solid glass articles. A basic glass batch mixture includes sand, soda ash, dolomite, limestone and sulfate (e.g. salt cake or gypsum). Additional materials may also be added which affect the final properties, e.g., color, transmittance, reflectance, optical properties etc., of the glass and/or melting characteristics of the batch. Known glass batch compositions are disclosed in U.S. Pat. Nos. 5,688,727; 5,352,640; 5,545,596; 5,837,629; 5,807,417; and 5,780,372, which are herein incorporated by reference. For example, coloring agents may be added to the batch components to achieve a desired final color of the glass. The particular batch components used and their relative amounts are selected based on the desired properties of the finished glass article and desired melting characteristics of the batch. 0004 In order to manufacture glass having solar control properties, such as heat absorbing or infrared absorbing glass, solar control materials, such as iron-containing materials may be added to the batch forming components. The iron may be present in both the ferrous, e.g., FeO, and ferric, e.g., Fe2O3, states. However, the relative amounts of ferrous and ferric iron in the final glass article have a direct effect on the color and also the optical and solar control properties of the glass article. For example, ferrous iron absorbs light in the infrared and visible regions and generally produces glass having a blue color. Ferric iron absorbs light in the ultraviolet and visible regions and generally produces glass having a yellow color. Thus, the solar control properties of the glass, e.g., transmittance, reflectance, absorbance, etc., can depend upon the amounts of ferrous and ferric iron in the glass. 0005 Rouge is well known and is conventionally used as a convenient source of iron when manufacturing solar control glass. However, rouge consists principally of ferric iron. Therefore, in order to produce infrared absorbing glass, it is necessary to chemically reduce at least a portion of this ferric to ferrous iron. This reduction is typically done by adding a carbon source, e.g., coal, graphite, sugar solution, etc., to the batch of glass forming components to facilitate the reduction of ferric iron to ferrous iron to increase the redox ratio of the glass, as defined hereinbelow. For high performance, infrared absorbing glass articles and compositions, redox ratios greater than about 0.3 are desirable. However, it is very difficult to obtain such a high redox ratio utilizing currently available glass production methods due principally to heat transfer difficulties. For example, in overhead heated furnaces, a layer of silica scum may form on top of the melt when large amounts of coal are added. The scum layer inhibits thermal transfer and hence may make it difficult to adequately heat the interior of the melt. 0006 To increase the redox ratio, typically the amount of oxidizing agent, e.g., sulfate material such as salt cake or gypsum, added to the batch is decreased and large amounts of both rouge and carbon are added to the glass batch mixture to achieve a desired higher level of ferrous iron in the batch and hence in the resulting glass article. However, a major drawback of decreasing sulfate addition and adding more carbon is that the melting quality of the batch becomes poorer and the formation of silica scum increases, which in turn further reduces thermal transfer into the glass melt and can lead to unmelted silica stone defects. This places a practical limit on the total amount of carbon that can be added. Additionally, since the carbon is typically added in the form of coal, an increase in the amount of coal may also increase the amount of gaseous sulfur byproducts, e.g., SO2, which may be produced during the glass making process due to a reaction between salt cake or gypsum and the coal. Treatment of such sulfur byproducts before release into the atmosphere may increase the cost of glass production. Further, while the addition of more rouge does lead to a higher amount of ferrous iron, it also produces a higher amount of ferric iron in the glass article and a higher total iron concentration in the glass. As the total iron concentration increases, the visible light transmittance of the glass decreases. For some commercial applications such as automotive windshield transparencies or architectural windows, it is desirable to produce a glass product which is infrared absorbing but also has a relatively high visible light transmittance, i.e., a glass product having a low total iron content which is highly reduced from Fe2O3 to FeO and with a transmittance of greater than about 60%, preferably greater than about 70% for windshields or sidelights for use in the United States. 0007 Attempts have been made to produce glass products having good infrared absorption, i.e., glass which is high in ferrous iron, but which also has good visible light transmittance. For example, U.S. Pat. No. 5,478,783, herein incorporated by reference, discloses a glass production method in which selenium and cobalt containing coloring agents are added to the batch and wuestite is used instead of rouge as the source of Fe2O3. However, the degree of reduction is critical and must not be greater than 21.34%. Higher reduction causes the glass to become too dark and the melting process difficulty increases due to poor heat penetration into the melt. 0008 U.S. Pat. Nos. 5,523,263 and 5,641,716, herein incorporated by reference, disclose glass production methods in which ilmenite (FeTiO3) is added to the batch as a source of titanium and as a partial source of Fe2O3. 0009 EP 765,846 and U.S. Pat. No. 5,888,264, herein incorporated by reference, disclose a method of preparing ferrous containing glass by adding a fayalite containing material to the batch. However, no disclosure is given regarding the relationship between fayalite and coal as glass batch components or how the fayalite affects the final redox ratio. 0010 It would be advantageous to provide a method of making glass and a glass product having a relatively high redox, e.g., greater than about 0.3, ratio with a total iron content of about 0.2-2.0 wt. %, preferably 0.25-1 wt. %, where the method does not have the drawbacks of the above-discussed conventional glass making procedures. It would also be advantageous to provide a glass making method which reduces or eliminates the need for the addition of carbon, e.g., coal, to the glass forming components.

SUMMARY OF THE INVENTION 0011 Glass is made from batch components having a source of ferrous iron added to the batch components to give a concomitant higher level of ferrous iron in the resulting glass product. Producing glass with a redox ratio above about 0.25 is an aspect of the invention. The iron source is preferably an iron silicate material, such as fayalite (2FeO.SiO2), iron garnet (3FeO.Fe2O3.3SiO2), magnesium-iron olivine (2(Mg,Fe)O.SiO2), grunerite (6FeO.8SiO2.Fe(OH)2), actinolite (CaO.3(Mg,Fe)O.4SiO2) or iron rich anthophyllite ((Mg,Fe)O.SiO2) or any combination thereof. The presence of a ferrous iron source in the glass batch components decreases or eliminates the need for carbon and also leads to a glass article having a relatively high redox ratio, e.g., greater than about 0.25. Due to the presence of silicate in the iron source, the amount of sand present in the batch is preferably reduced in proportion to the amount of silicate present in the added iron source. Glass compositions formed from such batch components may have a total iron amount in the range of about 0.2-2.0 wt. of the glass composition. 0012 A suitable basic batch composition for forming a soda-lime glass article of the invention generally can include about 48 to 72 wt. % silica material, e.g., sand; about 14 to 28 wt. % of a sodium material such as soda ash; about 0 to 19 wt. % of a calcium and magnesium material such as dolomite; about 0 to 15 wt. % of a calcium carbonate material such as limestone, and about 0.15 to 6.50 wt. % of a ferrous iron source, e.g., a ferrous silicate source such as fayalite. It should be appreciated that the batch composition may include other typical soda-lime glass batch additives or small amounts of other materials, such as an oxidizing material, such as a sulfate material, e.g., about 0-2.3 wt. % of gypsum, melting and refining aids, tramp materials or impurities. It should be further appreciated that additional materials may be added to color the glass and/or improve its solar performance. Rouge may also be added to the batch composition to increase the ferric iron and total iron content as desired. The batch may also have one or more colorant components such as elements or compounds of Ti, Se, Co, Cr, Ni, Mn, Ce, V, Mo or Cu intentionally added to modify the color of the glass, particularly with higher redox. Also, the batch may have 0 to 95 wt. of cullet of any type known to those skilled in the art. The batch is preferably substantially free of ferric iron. The batch may further include Al2O3 containing materials such as nepheline syenite or feldspar to produce glass having about 1 wt. % alumina to improve the chemical and stain durability of the glass.

BRIEF DESCRIPTION OF THE DRAWING 0013 FIG. 1 is a graph of FeO efficiency versus the amount of fayalite or EG-14 in the glass batch materials.

DESCRIPTION OF THE INVENTION 0014 The iron oxides in the glass composition perform several functions. Ferric oxide (Fe2O3) is a good ultraviolet radiation absorber and operates as a yellow colorant in the glass. Ferrous oxide (FeO) is a good infrared radiation absorber and operates as a blue colorant. The total amount of iron present in the glasses disclosed herein is expressed in terms of Fe2O3 in accordance with standard analytical practice, but that does not imply that all of the iron is actually in the form of Fe2O3. Likewise, the amount of iron in the ferrous state is reported as FeO, even though it may not actually be present in the glass as FeO. In order to reflect the relative amounts of ferrous and ferric iron in the glass compositions, the term redox shall mean the amount of iron in the ferrous state (expressed as FeO) divided by the amount of total iron (expressed as Fe2O3). Furthermore, unless stated to the contrary, the term total iron shall mean total iron expressed in terms of Fe2O3, the term Fe2O3 shall mean iron in the ferric state expressed in terms of Fe2O3 and the term FeO shall mean iron in the ferrous state expressed in terms of FeO. The amount of ferrous iron oxide is multiplied by a conversion factor of 1.111 to obtain a Fe2O3equivalent. 0015 In order to produce a solar control glass article having a relatively high iron redox ratio, e.g., greater than about 0.3, an iron source comprising ferrous iron is added to the glass batch components in accordance with the invention. This iron source preferably comprises an iron silicate source having ferrous iron, such as fayalite (2FeO.SiO2), iron garnet (3FeO.Fe2O3.3SiO2), magnesium-iron olivine (2(Mg,Fe)O.SiO2), grunerite (6FeO.8SiO2.Fe(OH)2), actinolite (CaO.3(Mg,Fe)O.4SiO2) or iron rich anthophyllite ((Mg,Fe)O.SiO2). Fayalite occurs naturally as a mineral or may be prepared synthetically. Other sources of fayalite include slags produced from molybdenum smelting or copper production processes. Fayalite is more resistant to oxidation during the glass making process than ferrous iron oxides, such as FeO or Fe3O4. 0016 In order to help prevent the ferrous iron from reoxidizing to ferric iron during the melting of the glass batch components, a reducing agent, e.g., a carbon source such as graphite, coal, preferably anthracite coal, or an aqueous or nonaqueous sugar containing material may be added to the glass batch of the invention. However, the amount of the carbon source, e.g., coal, required in the practice of the invention is less than that needed when rouge is the only source of iron. Therefore, such a reduction alleviates some of the problems associated with such coal addition. As discussed in more detail hereinbelow, to achieve a desired iron redox ratio in the glass article, the amount of coal added to the glass batch is directly related to the amount of ferrous source added to the glass batch components. The amount of ferrous iron in the glass article, and hence the amount of ferrous source added to the glass batch components, will depend upon the use contemplated for the glass article and what solar control properties are desired. However, a suitable finished article, e.g., flat glass, should comprise about 0.2-2.0% by weight of total iron including both ferrous and ferric iron with the redox ratio greater than about 0.25. 0017 A suitable basic batch composition of the invention can include 48 to 72 wt. % of silica material, e.g., sand; 14 to 28 wt. % of soda ash; 0 to 19 wt. % of dolomite; 0 to 15 wt. % of limestone and about 0.15 to 6.50 wt. % of an iron source, preferably a ferrous iron source such as one or more iron silicates. Additionally, an oxidizing material, such as 0.10 to 2.30 wt. % of sulfate material, e.g., gypsum or salt cake, may be added. Further, 0.01 to 0.50 wt. % of coal may be included in the batch as a chemical reducing agent. The sulfate material helps reduce bubble defects. During refining, the sulfate material yields sulfur dioxide and oxygen. 0018 It should be appreciated that the glass batch composition of the invention may include small amounts of other materials, for example melting and refining aids, tramp materials or impurities, such as elements or compounds of sodium, potassium, calcium, magnesium, manganese, aluminum, sulfur, strontium, zirconium, chlorine, cobalt, nickel, selenium, chromium, molybdenum, barium, titanium, cerium, tin, zinc or iron. 0019 It should be further appreciated that additional materials may be included to color the glass or improve its solar performance, such as elements or compounds of titanium, selenium, cobalt, cerium, vanadium, molybdenum, chromium, nickel, manganese or copper. Generally, as the amount of the colorants increases in the glass composition, the visible, IR and UV transmittance decreases. As materials are added to change the glass color or enhance solar performance, care must be taken to maintain the visible light transmittance and color required for that particular application. It should be remembered that changing the thickness of the glass will affect the spectral properties so that a particular composition which has acceptable color and performance at a particular thickness may not be acceptable at a different thickness. 0020 Additionally, cullet may be added to the batch composition before or during melting. The cullet may be clear or may include coloring agents such as those discussed above. The cullet may also include iron in either the ferrous or ferric states, although the ferrous state is desired for most solar control glass products. 0021 Additionally, the amount of sulfate, typically sodium sulfate or calcium sulfate, added to the glass batch components may be reduced to slow down the oxidation of ferrous iron oxide to ferric iron oxide. 0022 The glass of the present invention may be melted and refined in a continuous, large-scale, commercial melting operation and formed into flat glass sheets of varying thickness 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. It should be appreciated that as a result of forming the glass on molten tin, measurable amounts of tin oxide may migrate into surface portions of the glass on the side that was in contact with the tin. Typically, a piece of float glass has an SnO2 concentration of at least about 0.05 wt. % in the first few microns below the surface of the glass that was in contact with the tin. 0023 Although it is preferred that the glass disclosed herein be made using a conventional, overhead fired continuous melting operation, as is well known in the art, the glass may also be produced using a multi-stage melting operation as disclosed, for example, in U.S. Pat. Nos. 4,381,934; 4,792,536; or 4,886,539. If required, a stirring arrangement may be employed within the melting and/or forming stages of the glass production operation to homogenize the glass in order to produce glass of high optical quality.

COMPARATIVE EXAMPLE 0024 As a reference point for purposes of the following discussion, Table I shows a sample batch composition (laboratory batch) for the formation of flat glass based on conventional Solargreen(D glass manufactured by PPG Industries, Inc. of Pittsburgh, Pennsylvania. This system will be referred to herein as a standard Solargreen system. All of the amounts listed in Table I are in grams with equivalent wt. in parentheses. The batch composition includes rouge as a source of iron and coal and gypsum to control the reduction of ferric iron to ferrous iron. 1TABLE IBatchComponentsSolargreen batchSand500.00 (59.63)Soda ash164.50 (19.62)Dolomite121.00 (14.43)Limestone37.40 (4.46)Gypsum7.40 (0.88)TiO22.04 (0.24)Rouge5.70 (0.68)Coal0.40 (0.048)

0025 These batch components were placed in a four-inch Lavasil crucible and heated at 2650 F. for two hours in an electric furnace in an air atmosphere. The melt was fritted in water and heated again for one hour at 2650 F. The melt was then fritted a second time in water, reheated for two hours at 2650 F., then cast into a slab and annealed at 1100 F. The resultant glass (690 g) slab was analyzed by x-ray fluorescence and the results are shown in Table II as weight percentages. The FeO control in Table II was determined by a wet chemical analysis method 2TABLE IISolargreenglassSiO273.74Na2O12.90K2O0.035CaO8.33MgO3.62Al2O30.14SO30.172Fe2O30.737SrO0.004ZrO20.003Cl0.004CoO<0.0003NiO<0.0003Se<0.0003Cr2O30.0004MnO20.0032Mo<0.0005BaO0.01TiO20.304CeO2<0.01SnO2<0.001ZnO<0.001FeO0.136Redox0.185

0026 Thus, as shown in Table II, the standard Solargreen glass had a redox ratio of 0.185. Since the only source of iron was the rouge, this means that all of the FeO in the glass (690 g0.136% FeO0.94 g FeO) had to come from the 5.7 g of rouge. Looking at this as an efficiency, ire., how much of the starting iron source material is converted to or remains in the FeO state, 0.94 g FeOconversion factor of 1.111 to convert to an equivalent of Fe2O35.70 g of the starting iron source material18.2%. Thus, in this melt, only about 18.2% of the rouge is reduced to FeO. With respect to the reducing power of coal in this system, 0.94 g FeO formed0.4 g coal in the starting material2.35 g FeO produced per gram of coal. 0027 With this Solargreen glass system as a reference, the use of an iron silicate source rather than rouge in accordance with the invention will be discussed with particular reference to the following examples.

Example 1 0028 Glass melts were made in similar manner to the standard Solargreen glass system described above to determine the effect of using fayalite as a source of ferrous iron on the redox ratio of the resulting glass article. The source of fayalite was EG-14, commercially available from Barnes Environmental, Inc. of Waterdown, Ontario. EG-14 is about 23.0% Feo which is equivalent to 25.53% Fe2O3 (23.0%1.11125.53%). Table III shows the batch components for a first sample batch (S-1) and second sample batch (S-2) compared to that of the standard Solargreen batch system. The batches S-1 and S-2 are similar to the standard Solargreen glass batch described above except that in S-1 a fayalite source (EG-14) is used as an iron source with no coal present and in S-2 both fayalite and coal are present in the batch materials. All of the amounts listed in Table III are in grams with equivalent wt. % in parentheses. 3TABLE IIIBatch ComponentsS-1 batchS-2 batchSolargreen batchSand500.00500.00500.00(59.37)(59.38)(59.63)Soda ash164.50164.00164.50(19.53)(19.48)(19.62)Dolomite121.00121.00121.00(14.37)(14.37)(14.43)Limestone37.4037.4037.40(4.44)(4.44)(4.46)Gypsum7.407.407.40(0.88)(0.88)(0.88)TiO22.042.042.04(0.24)(0.24)(0.24)EG-149.839.830(1.17)(1.17)Rouge005.70(0.68)Coal00.400.40(0.048)(0.048)

0029 The S-1 and S-2 batches were placed in separate four-inch Lavasil crucibles and melted for two hours at 2650 F. in an electric furnace in an air atmosphere. The melts were fritted in water and again heated for one hour at 2650 F. The melts were fritted a second time in water and reheated for two more hours at 2650 F. The melts were then cast into a slab and annealed at 1100 F. The resultant glass slab (690 g) was then analyzed by x-ray fluorescence, and the results are shown in Table IV in weight percent. 4TABLE IVS-1 glassS-2 glassSolargreen glassS1O273.7473.6473.74Na2O12.8112.9012.90K2O0.0390.0400.035CaO8.328.368.33MgO3.613.623.62Al2O30.180.190.14SO30.1710.1070.172Fe2O30.7930.8000.737SrO0.0040.0040.004ZrO20.0030.0030.003Cl0.0050.0070.004CoO0.00120.0011<0.0003NiO<0.0003<0.0003<0.0003Se<0.0003<0.0003<0.0003Cr2O30.00160.00130.0004MnO20.00370.00340.0032Mo<0.0005<0.0005<0.0005BaO0.010.010.01TiO20.2590.2630.304CeO2<0.01<0.01<0.01SnO2<0.001<0.001<0.001ZnO0.050.05<0.001FeO0.1580.2080.136Redox0.1990.2600.185

0030 As shown in Table IV, the redox ratio of the glass made from the S-1 melt (0.199) containing fayalite is higher than that of the standard Solargreen glass discussed above (0.185). However, the glass made from the S-2 melt containing both fayalite and coal has a higher redox ratio than that of the S-1 glass with fayalite alone. From Example 1, it can be seen that if the same level of coal is used in two glass batches (e.g., the S-2 batch and standard Solargreen batch) but fayalite is substituted for rouge, the redox ratio of the resulting glass product increases by about 0.07-0.08. From Table IV, it appears that about 9.83 grams of EG-14 per 500 g of sand (S-1) are roughly equivalent to the reducing power of about 0.4 grams of coal per 500 g of sand. Therefore, to maintain a desired redox ratio in the final glass product but using added fayalite, coal should be present but the amount of coal in the glass batch can be reduced by about 0.8 g per 1,000 g of sand for every 19.66 g of EG-14 added per 1,000 g of sand. This relationship could vary with other glass batch systems. For example, decreasing the amount of salt cake (gypsum) will increase the redox ratio and decreasing the amount of coal will decrease the redox ratio. 0031 Turning to the relationship between iron silicate and coal addition in this system, the S-1 glass had 1.09 grams FeO in the final glass (690 grams of glass X 0.158% FeO). The S-2 glass had 1.44 grams FeO. However, for S-1 glass, 2.26 grams of FeO were added per 500 grams of sand (9.83 grams EG-1423.0% FeO). EG-14 contains 32.6 wt % fayalite and fayalite is 70.51% FeO, thus equating to 23.0% FeO. Looking at this as an efficiency, 1.09 grams FeO in the final glass/2.26 grams FeO added 48.2%, which is much higher than the 18.2% efficiency for the standard Solargreen system described above. This means that 48.2% of the initial Feo remained in the ferrous state and 51.8% of the FeO was converted to the ferric state. Using a similar calculation, the S-2 glass had an efficiency of 63.7%. 0032 Looking at this another way, 0.94 gram FeO in the standard Solargreen system divided by 0.4 gram of coal added equals 2.35 gram FeO produced per gram of coal. 1.09 gram FeO in the final glass divided by 2.26 gram of FeO from iron silicate equals 0.48 gram FeO produced per gram of FeO in iron silicate. 2.35 grams of FeO/gram coal divided by 0.48 gram FeO/gram FeO in iron silicate equals 4.9 gram FeO in iron silicate per of gram coal.

Example 2 0033 Table V shows the batch compositions in grams for two additional fayalite containing sample glass batches S3 and S4. Batches S3 and S4 are similar to the batches described above but contain less fayalite, e.g., 7.1 g of EG-14. However, sample S3 contains no coal while sample S4 contains 0.2 g of coal. The melts were processed in similar manner as described above in Example 1, and the analyses of the resulting glass articles are shown in Table VI. 5TABLE VS3S4Sand500.00 (59.57)500.00 (59.55)Soda ash164.5 (19.60)164.5 (19.60)Dolomite121.0 (14.42)121.0 (14.41)Limestone37.4 (4.46)37.4 (4.45)Gypsum7.4 (0.88)7.4 (0.88)TiO22.0 (0.24)2.0 (0.24)EG-147.1 (0.85)7.1 (0.85)Coal00.2 (0.024)

0034

6TABLE VIS3S4SiO273.8173.82Na2O12.9012.90K2O0.0370.038CaO8.378.35MgO3.643.63Al2O30.170.20SO30.1520.149Fe2O30.5870.584SrO0.0050.005ZrO20.0050.003Cl0.0050.006CoO0.00090.0009NiO<0.00030.0003Se<0.0003<0.0003Cr2O30.00120.0012MnO20.00340.0028Mo<0.0005<0.0005BaO0.010.01TiO20.2570.256CeO2<0.01<0.01SnO2<0.001<0.001ZnO0.040.04FeO0.1160.118Redox0.1980.202

0035 In these samples also, the use of a small amount of coal (0.2 g) causes an increase in the redox ratio over a system with no coal. However, the relationships discussed above with respect to the extent of increased redox ratio in the modified Solargreen system do not appear to hold in this system. It is believed that this lower level of fayalite and coal addition are not sufficient to overcome the oxidizing effects of the salt cake addition and the air atmosphere inside the electric furnace that was used during melting of the laboratory glasses. 0036 Calculating the efficiencies of these systems as discussed above, S-3 had an efficiency of 49.0% while S-4 had an efficiency of 49.8%. 0037 FIG. 1 shows a graph of the efficiencies for the S-1 to S-4 systems and the standard Solargreen system of Table I versus the amount of EG-14 or fayalite in the batch material per 1000 lb. of sand. In FIG. 1, the symbols for the various systems are: A is the S-1 system, 0 is the S-2 system, O is the S-2 system at double the coal and V is the standard Solargreen system at double the amount of coal. FIG. 1 shows that the efficiency of the system increases by either adding coal or increasing the amount of fayalite. However, it appears from FIG. 1 that for the exemplary systems, more than about 0.4 lb. of coal for 1000 lb. of sand are needed to overcome the oxidizing effects of the gypsum and air atmosphere used in the production of the glass.

Illustrative Example 3 0038 Table VII shows theoretical batch compositions for several iron silicate containing batch materials (S6-S11) to produce glass having similar properties as a conventional glass batch (S5) made with rouge. The numbers are in grams with the equivalent weight percent in parentheses. 0039 These sample batches are presented to show that since the ferrous iron sources used in accordance with the invention are iron silicates, the amount of sand added to the batch should be reduced by an amount substantially equivalent to the amount of silicate introduced into the system. 7TABLE VIIS5S6S7S8S9S10S11Sand1000.00997.38996.85994.75999.25986.00989.51(59.90)(59.83)(59.77)(59.81)(59.93)(59.38)(59.50)Soda ash323.00323.00323.00323.00323.00323.00323.00(19.35)(19.38)(19.37)(19.42)(19.37)(19.45)(19.42)Limestone87.6087.6087.6096.3487.6090.5396.34(5.25)(5.25)(5.25)(5.79)(5.25)(5.45)(5.79)Dolomite242.50242.50242.50226.39242.50226.39226.39(14.53)(14.55)(14.54)(13.61)(14.54)(13.63)(13.61)Salt cake7.207.207.207.207.207.207.20(0.43)(0.43)(0.43)(0.43)(0.43)(0.43)(0.43)Rouge7.32000000(0.44)CoO0.0110.0110.0110.0110.0110.0110.011(0.0007)(0.0007)(0.0007)(0.0007)(0.0007)(0.0007)(0.0007)Fayalite08.87700000(0.53)Iron009.6770000garnet(0.58)Mg-iron00015.006000olivine(0.90)Grunerite00007.23100(0.43)Actinolite0000026.9950(1.63)Iron rich00000020.239antho-(1.22)phylliteCoal1.770.450.980.450.450.450.45(0.11)(0.03)(0.06)(0.03)(0.03)(0.03)(0.03)Total1669.401667.021667.821663.161667.241660.581663.14Salt4.0715.927.3515.9215.9215.9315.92cake/coalratio

0040 Comparing the relative iron compositions of the iron silicates with that of rouge on an atomic weight basis, fayalite (2FeO-SiO2) is theoretically 70.51 wt % FeO and 29.49% SiO2. Multiplying the FeO percentage of fayalite by 1.111 to convert this to an equivalent of Fe2O3, fayalite is theoretically equivalent to 78.34% Fe2O3 compared with rouge which is about 99% Fe2O3. Using similar calculations, iron garnet (3FeO.Fe2O3.SiO2) is 71.86% Fe2O3, magnesium iron olivine (2(Mg,Fe)O.SiO2) is 46.34% Fe2O3, grunerite (6FeO8SiO2 Fe(OH)2) is 96.17% Fe2O3, actinolite (CaO.3(Mg,Fe)O.4SiO2) is 25.76% Fe2O3 and iron rich anthophylite ((Mg,Fe)O.SiO2) is 34.36% Fe2O3. 0041 Glass compositions in accordance with the invention made by the float glass process may have a sheet thickness of about 1-10 mm. For vehicle glazing applications, it is preferred that the glass sheet made in accordance with the invention have a thickness of about 1.8-5 mm. When the glass is used in selected areas of a vehicle, e.g., the windshield and front door sidelights, the glass should have an LTA of at least about 70% for U.S. applications. In addition, the glass should have a TSUV of less than about 60%, preferably less than about 50%, a TSIR of less than about 35%, preferably less than about 30%, and a TSET of less than about 55%, preferably less than about 50% at a thickness of about 0.154 inch. 0042 Thus, by using an iron silicate material of the invention as a ferrous iron source, an increased efficiency for maintaining or converting iron oxide to FeO is obtained with an associated increase in iron redox ratio. The present invention is particularly useful for tinted flat glass applications such as automotive glass. 0043 It will be readily appreciated by those skilled in the art that modifications may be made to the invention without departing from the concepts disclosed in the foregoing description. Such modifications are to be considered as included within the scope of the invention. Accordingly, the particular embodiments described in detail hereinabove are illustrative only and are not limiting as to the scope of the invention, which is to be given the full breadth of the above disclosure and any and all equivalents thereof.