TW201736284A - Method and apparatus for making glass substrate capable of reducing the partial plate-thickness deviation generated by a glass substrate - Google Patents

Method and apparatus for making glass substrate capable of reducing the partial plate-thickness deviation generated by a glass substrate Download PDF

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TW201736284A
TW201736284A TW106109120A TW106109120A TW201736284A TW 201736284 A TW201736284 A TW 201736284A TW 106109120 A TW106109120 A TW 106109120A TW 106109120 A TW106109120 A TW 106109120A TW 201736284 A TW201736284 A TW 201736284A
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glass
molded body
molten glass
temperature
molten
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TW106109120A
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TWI725140B (en
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中嶋公彦
鈴木諒
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安瀚視特控股股份有限公司
安瀚視特韓國有限公司
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    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B17/00Forming molten glass by flowing-out, pushing-out, extruding or drawing downwardly or laterally from forming slits or by overflowing over lips
    • C03B17/06Forming glass sheets
    • C03B17/064Forming glass sheets by the overflow downdraw fusion process; Isopipes therefor
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B17/00Forming molten glass by flowing-out, pushing-out, extruding or drawing downwardly or laterally from forming slits or by overflowing over lips
    • C03B17/06Forming glass sheets
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B25/00Annealing glass products
    • C03B25/04Annealing glass products in a continuous way
    • C03B25/06Annealing glass products in a continuous way with horizontal displacement of the glass products
    • C03B25/08Annealing glass products in a continuous way with horizontal displacement of the glass products of glass sheets

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Glass Compositions (AREA)
  • Re-Forming, After-Treatment, Cutting And Transporting Of Glass Products (AREA)

Abstract

The purpose of the present invention is to provide a method for making a glass substrate with which it is possible to reduce the partial plate-thickness deviation generated by a glass substrate. A method of manufacturing the glass substrate, wherein the molten glass is supplied from the glass supply pipe to the molded body having a supply tank, is to use the molded body to form a flat-plate glass by the overflow pull-down method, and an uniform shape for the bottom surface is provided along the extending direction of the above-described supply tank and the width direction orthogonal to the extending direction of the supply tank where the molten glass is supplied thereto and overflown therefrom. The method for producing the glass substrate includes: a forming step of forming a maximum temperature difference of 30 DEG C or less from the glass supply pipe to the molten glass of the supply tank and the molten glass having a viscosity of 22,000 dPa.s or more and 38,000 dPa.s or less is supplied to the supply tank, and the molten glass is converged at the lower end of the molded body to form the flat glass; and an end-part cooling step in which the partial plate-thickness deviation generated by a glass substrate in the forming step is reduced, so that two ends of the flat glass along the width direction are cooled.

Description

玻璃基板之製造方法及玻璃基板之製造裝置Method for producing glass substrate and device for manufacturing glass substrate

本發明係關於一種玻璃基板之製造方法及玻璃基板之製造裝置。The present invention relates to a method for producing a glass substrate and a device for producing a glass substrate.

有時為製造用於液晶顯示器或電漿顯示器等平板顯示器之玻璃基板(以下,稱為「顯示器用玻璃基板」),而使用溢流下拉法。溢流下拉法包括藉由於成形爐中使熔融玻璃自成形體之上部溢出(overflow)而於成形體之下方成形板狀之平板玻璃之步驟、及使平板玻璃於緩冷爐中緩冷之冷卻步驟。於緩冷爐中,將平板玻璃引入成對之輥間,利用輥將平板玻璃一面搬送至下方一邊拉拔成所需之厚度後,將平板玻璃進行緩冷。此後,藉由將平板玻璃切斷為特定之尺寸而形成玻璃板。 沿著成形體之側面向下流動之熔融玻璃係於離開成形體之同時,因表面張力而於平板玻璃之寬度方向上收縮。於專利文獻1中,公開有如下方法,即,於成形體與成形體下方之張力輥之間,於平板玻璃之寬度方向之緣部附近,使用與平板玻璃相隔地設置之冷卻單元,調整平板玻璃之緣部之溫度,抑制平板玻璃之收縮。此後,收縮得以抑制之平板玻璃穿過緩冷空間而成形。於該緩冷空間中,環境溫度以成為所需之溫度分佈(玻璃板中不產生應變之溫度分佈)之方式得到控制,從而抑制玻璃板之板厚偏差、翹曲、應變。 [先前技術文獻] [專利文獻] [專利文獻1]日本專利特開平5-124827號公報In order to manufacture a glass substrate (hereinafter referred to as a "glass substrate for display") for a flat panel display such as a liquid crystal display or a plasma display, an overflow down-draw method is used. The overflow down-draw method includes a step of forming a plate-shaped flat glass under the molded body by overflowing the molten glass from the upper portion of the molded body in the forming furnace, and cooling the flat glass in the slow cooling furnace step. In the slow cooling furnace, the flat glass is introduced into the pair of rolls, and the flat glass is pulled to the lower side by a roll and pulled to a desired thickness, and then the flat glass is slowly cooled. Thereafter, the glass plate is formed by cutting the flat glass into a specific size. The molten glass flowing downward along the side surface of the molded body is caused to contract from the molded body while being contracted in the width direction of the flat glass by the surface tension. Patent Document 1 discloses a method of adjusting a flat plate between a molded body and a tension roller below the molded body in the vicinity of the edge portion in the width direction of the flat glass by using a cooling unit provided separately from the flat glass. The temperature at the edge of the glass suppresses the shrinkage of the flat glass. Thereafter, the flat glass whose contraction is suppressed is formed by passing through the slow cooling space. In the slow cooling space, the ambient temperature is controlled so as to become a desired temperature distribution (temperature distribution in which no strain occurs in the glass sheet), thereby suppressing variations in sheet thickness, warpage, and strain of the glass sheet. [Prior Art Document] [Patent Document] [Patent Document 1] Japanese Patent Laid-Open No. Hei 5-124827

[發明所欲解決之問題] 近年來,於液晶顯示裝置用玻璃基板中,對規格(品質)之要求日益嚴格。對玻璃基板之表面要求較高之平坦性,為滿足要求規格,尤其必須抑制陡峭之凹或凸導致條紋(striae)或局部之板厚偏差之產生。該條紋係於特定之寬度中平板玻璃之厚度(高度)變動所致之凹凸,且於離開成形體之同時,因表面張力而於平板玻璃之寬度方向上收縮所致,且於平板玻璃之搬送方向上紋路狀連續地產生。 因此,本發明之目的在於提供一種可抑制平板玻璃上產生之包括條紋之局部之板厚偏差之玻璃基板之製造方法及玻璃基板之製造裝置。 [解決問題之技術手段] 本發明之一態樣係一種將熔融玻璃自玻璃供給管供給至具有供給槽之成形體,且使用上述成形體藉由溢流下拉法成形平板玻璃之玻璃基板之製造方法。於該製造方法中,上述供給槽具有供給至上述供給槽之熔融玻璃自上述供給槽溢出之量於上述供給槽之延伸方向及與上述延伸方向正交之寬度方向上形成均一之底面形狀,上述玻璃基板之製造方法具有:成形步驟,其係將自上述玻璃供給管供給至上述供給槽之熔融玻璃之最大溫度差為30℃以下且熔融玻璃之黏度為22000 dPa・s以上38000 dPa・s以下之熔融玻璃供給至上述供給槽,且於上述成形體之下端使上述熔融玻璃匯流,成形平板玻璃;及端部冷卻步驟,其係以抑制於上述成形步驟中成形所得之上述平板玻璃中局部產生之板厚偏差之方式,將平板玻璃之寬度方向之兩端部冷卻。 於上述端部冷卻步驟中,較佳為將上述成形體於上述平板玻璃之寬度方向上未變形時所施加且上述平板玻璃之剖面形狀成為目標形狀之張力設為基準張力,於上述成形體未變形時,以藉由將上述平板玻璃之寬度方向之兩端部冷卻而成為上述基準張力之方式進行控制,且於上述成形體產生變形時,對於上述平板玻璃施加根據上述成形體之變形而與上述基準張力相加之張力。 此時,較佳為,上述成形體之變形係伴隨著上述成形體之使用而經時變化之蠕變變形,且對上述基準張力加上與上述蠕變變形造成之上述成形體之特定位置之位移量相應之張力。又,較佳為,上述變形愈大則愈增強上述兩端部之冷卻。較佳為,上述板厚偏差為10 μm以下。較佳為,於上述成形步驟中,以於上述成形體中向下流動之熔融玻璃之溫度相較上述熔融玻璃之液相溫度增高10℃~150℃之方式,加熱上述熔融玻璃。本發明之其他一態樣係一種將熔融玻璃自玻璃供給管供給至具有供給槽之成形體,且使用上述成形體藉由溢流下拉法成形平板玻璃之玻璃基板之製造裝置。上述成形體具有接收最大溫度差為30℃以下且黏度為22000 dPa・s以上38000 dPa・s以下之熔融玻璃之供給之供給槽、及用以於上述成形體之下端使上述熔融玻璃匯流而成形平板玻璃之壁面。上述供給槽具有供給至上述供給槽之熔融玻璃自上述供給槽溢出之量於上述供給槽之延伸方向及與上述延伸方向正交之寬度方向上形成均一之底面形狀。 上述製造裝置更具備以抑制利用上述成形體成形所得之上述平板玻璃中局部產生之板厚偏差之方式冷卻平板玻璃之寬度方向之兩端部之端部冷卻裝置。 [發明之效果] 根據上述態樣之玻璃基板之製造方法及玻璃基板之製造裝置,可抑制平板玻璃中產生之局部性板厚偏差。[Problems to be Solved by the Invention] In recent years, the requirements for specifications (quality) have become increasingly strict in glass substrates for liquid crystal display devices. The flatness of the surface of the glass substrate is required to be high, and in order to meet the required specifications, it is particularly necessary to suppress the occurrence of streaks or partial thickness variations of the steep concave or convex streaks. The stripe is formed by the unevenness due to the variation in the thickness (height) of the flat glass in a specific width, and is caused by the surface tension due to the surface tension being contracted in the width direction of the flat glass, and is conveyed on the flat glass. The grain shape is continuously generated in the direction. Accordingly, an object of the present invention is to provide a method for producing a glass substrate and a glass substrate manufacturing apparatus which can suppress variation in thickness of a portion including streaks which are generated on a flat glass. [Technical means for solving the problem] One aspect of the present invention is a method of manufacturing a glass substrate in which molten glass is supplied from a glass supply pipe to a molded body having a supply groove, and the flat body glass is formed by an overflow down-draw method using the above-described molded body. method. In the manufacturing method, the supply tank has a uniform bottom surface shape in which the molten glass supplied to the supply tank overflows from the supply tank in a direction in which the supply groove extends and a width direction orthogonal to the extending direction. The method for producing a glass substrate includes a molding step of a maximum temperature difference of 30° C. or less between the molten glass supplied from the glass supply tube to the supply tank, and a viscosity of the molten glass of 22,000 dPa·s or more and 38,000 dPa·s or less. The molten glass is supplied to the supply tank, and the molten glass is condensed at a lower end of the molded body to form a flat glass; and an end portion cooling step is performed to suppress localized generation in the flat glass obtained by molding in the forming step. In the manner of the thickness deviation of the plate, both ends of the flat glass in the width direction are cooled. In the end portion cooling step, it is preferable that the tension applied when the molded body is not deformed in the width direction of the flat glass and the cross-sectional shape of the flat glass is a target shape is used as a reference tension, and the molded body is not At the time of deformation, the both ends of the flat glass in the width direction are cooled to be the reference tension, and when the molded body is deformed, the flat glass is subjected to deformation according to the molded body. The tension is added by the above reference tension. In this case, it is preferable that the deformation of the molded body is a creep deformation which changes with time with the use of the molded body, and a specific position of the molded body due to the creep deformation is added to the reference tension. The amount of displacement corresponds to the tension. Further, it is preferable that the larger the deformation is, the more the cooling of the both end portions is enhanced. Preferably, the thickness deviation is 10 μm or less. Preferably, in the forming step, the molten glass is heated so that the temperature of the molten glass flowing downward in the formed body is increased by 10 to 150 ° C from the liquidus temperature of the molten glass. Another aspect of the present invention is a manufacturing apparatus for supplying molten glass from a glass supply pipe to a molded body having a supply groove, and forming a glass substrate of the flat glass by the overflow down-draw method using the molded body. The molded body has a supply groove for receiving a supply of molten glass having a maximum temperature difference of 30 ° C or less and a viscosity of 22,000 dPa·s or more and 38,000 dPa·s or less, and a molten groove for forming a molten glass at a lower end of the molded body. The wall of the flat glass. The supply tank has a uniform bottom surface shape in which the molten glass supplied to the supply tank overflows from the supply tank in a direction in which the supply groove extends and a width direction orthogonal to the extending direction. Further, the manufacturing apparatus further includes an end portion cooling device that cools both end portions in the width direction of the flat glass so as to suppress variation in thickness locally generated in the flat glass obtained by molding the molded body. [Effect of the Invention] According to the method for producing a glass substrate and the apparatus for producing a glass substrate of the above aspect, variation in local thickness caused in the sheet glass can be suppressed.

以下,對本實施形態之玻璃基板之製造方法進行說明。 (玻璃基板之製造方法之整體概要) 圖1係表示本實施形態之玻璃基板之製造方法之步驟之一例之圖。玻璃基板之製造方法主要具有:溶解步驟(ST1)、澄清步驟(ST2)、均質化步驟(ST3)、供給步驟(ST4)、成形步驟(ST5)、緩冷步驟(ST6)、及切斷步驟(ST7)。其他亦可具有研削步驟、研磨步驟、清洗步驟、檢查步驟、捆包步驟等。製造所得之玻璃基板視需要於捆包步驟中積層後,搬送至訂貨方之業者。 溶解步驟(ST1)係藉由將玻璃原料加熱而製成熔融玻璃。 澄清步驟(ST2)係藉由使熔融玻璃升溫,而產生包含熔融玻璃中所含之氧、CO2 或SO2 之泡。該泡係吸收因熔融玻璃中所含之澄清劑(氧化錫等)之還原反應而產生之氧進行成長,且漂浮至熔融玻璃之液面而釋放。此後,於澄清步驟中,因使熔融玻璃之溫度下降,故利用澄清劑之還原反應所得之還原物質進行氧化反應。藉此,熔融玻璃中殘存之泡中之氧等氣體成分被再次吸收至熔融玻璃中,從而泡破滅。澄清劑所進行之氧化反應及還原反應係藉由控制熔融玻璃之溫度而進行。 再者,澄清步驟亦可採用使存在於熔融玻璃中之泡於減壓環境下成長後消泡之減壓消泡方式。減壓消泡方式於不使用澄清劑之方面較為有效。然而,減壓消泡方式導致裝置複雜化及大型化。因此,較佳為採用使用澄清劑,使熔融玻璃溫度上升之澄清方法。 均質化步驟(ST3)係藉由使用攪拌器攪拌熔融玻璃,而進行玻璃成分之均質化。藉此,可減少作為條紋等原因之玻璃之組成不均。均質化步驟係於下述之攪拌槽中進行。 供給步驟(ST4)係將經攪拌之熔融玻璃供給至成形裝置。 成形步驟(ST5)及緩冷步驟(ST6)係於成形裝置中進行。 成形步驟(ST5)係將熔融玻璃成形為平板玻璃,製成平板玻璃流。成形中,採用溢流下拉法。 緩冷步驟(ST6)係將成形後流動之平板玻璃以達到所需之厚度,且不產生內部應變之方式,進而不產生翹曲之方式進行冷卻。 切斷步驟(ST7)係藉由將緩冷後之平板玻璃切斷為特定之長度,而獲得板狀之玻璃基板。切斷所得之玻璃基板進而被切斷為特定之尺寸,製成目標尺寸之玻璃基板。 圖2係進行本實施形態中之溶解步驟(ST1)~切斷步驟(ST8)之玻璃基板之製造裝置之概略圖。玻璃基板之製造裝置係如圖2所示主要具有溶解裝置100、成形裝置200、及切斷裝置300。溶解裝置100具有溶解槽101、澄清管102、攪拌槽103、傳輸管104、105、及玻璃供給管106。 於圖2所示之溶解槽101中,設置有未圖示之燃燒器等加熱機構。對溶解槽投入已添加澄清劑之玻璃原料,進行溶解步驟(ST1)。溶解槽101中已熔融之熔融玻璃係經由傳輸管104供給至澄清管102。 於澄清管102中,調整熔融玻璃MG之溫度,利用澄清劑之氧化還原反應進行熔融玻璃之澄清步驟(ST2)。具體而言,藉由使澄清管102內之熔融玻璃升溫,含有熔融玻璃中所含之氧、CO2 或SO2 之泡吸收因澄清劑之還原反應而產生之氧進行成長,且漂浮至熔融玻璃之液面後釋放至氣相空間。此後,藉由使熔融玻璃之溫度下降,因澄清劑之還原反應所得之還原物質進行氧化反應。藉此,熔融玻璃中殘存之泡中之氧等氣體成分被再次吸收至熔融玻璃中,從而泡破滅。澄清後之熔融玻璃係經由傳輸管105供給至攪拌槽103。 於攪拌槽103中,藉由攪拌棒103a來攪拌熔融玻璃進行均質化步驟(ST3)。攪拌槽103中得以均質化之熔融玻璃係經由玻璃供給管106供給至成形裝置200(供給步驟ST4)。 於成形裝置200中,藉由溢流下拉法而自熔融玻璃成形平板玻璃SG(成形步驟ST5),且進行緩冷(緩冷步驟ST6)。 於切斷裝置300中,形成自平板玻璃SG切取所得之板狀之玻璃基板(切斷步驟ST7)。 供給步驟S4係控制於玻璃供給管106之中流動之熔融玻璃之溫度。具體而言,將玻璃供給管106通電加熱,從而將於玻璃供給管106之中流動之熔融玻璃加熱,且利用耐火材料將玻璃供給管106包圍,藉此,抑制於玻璃供給管106之中流動之熔融玻璃之散熱。於供給步驟S4中,以於玻璃供給管106之中流動之熔融玻璃之溫度自上游側朝向下游側逐漸降低之方式,控制熔融玻璃之溫度。玻璃供給管106係區分為複數個區,且熔融玻璃之溫度按區進行控制。加熱玻璃供給管106之通電加熱裝置係基於測定裝置之測定資料,以熔融玻璃之溫度呈現變化之方式,控制流入玻璃供給管106之各區之電流及電壓。可藉由於玻璃供給管106中控制電流及電壓,而將供給至成形裝置200之熔融玻璃之溫度適當地變更。此處,於玻璃供給管106之下游側之端部,管溫度及熔融玻璃之中心溫度較佳為1235℃~1265℃,更佳為1240℃~1260℃。 (成形體之構成) 繼而,參照圖3及圖4,對成形裝置200所具備之成形體1之構成進行說明。於圖3中,表示可用於本實施形態之製造方法之成形體1之一例,於圖4中,表示使用圖3所示之成形體1之本實施形態之製造方法中之成形步驟之一例。成形體1具備:上表面3,其係形成有供給熔融玻璃之供給槽2;一對壁面5(圖3、4中僅圖示了一壁面),其等係引導自供給槽2之兩側溢出後自上表面3中之供給槽2所延伸之方向之兩端部3a、3b之間向下流動之熔融玻璃,於成形體1之下端4匯合成為平板玻璃SG;及一對導件6a、6b,其等係形成於壁面5之寬度方向上之兩端部5a、5b之位置處。導件6a、6b係分別以於端部5a、5b之位置處自壁面5突出之方式相互對向地形成。自供給槽2溢出之熔融玻璃係於一對壁面5之各者向下流動。壁面5具有自供給槽2溢出之熔融玻璃於鉛垂方向上向下流動之垂直壁面、及將於垂直壁面向下流動之熔融玻璃導向成形體1之下端4且與垂直壁面連接之傾斜壁面。於壁面5向下流動之熔融玻璃之一對流體係於成形體1之下端4匯流,從而相互地交匯。此時,藉由導件6a、6b而限制沿著壁面5向下流動之熔融玻璃之寬度,從而連續地形成例如寬度方向之厚度均一性較高之平板玻璃SG。成形體1之下端4形成一對壁面5彼此(傾斜壁面彼此)連接而成之直線狀棱線。圖3、4所示之符號2a係供給槽2之底面2a,圖3所示之符號7係供給至供給槽2之熔融玻璃之液面7。 此處,成形體1之供給槽2具有如下之底面2a之形狀,該底面2a之形狀係供給至供給槽2之熔融玻璃自供給槽2溢出之量於供給槽2之延伸方向(熔融玻璃之流動方向)、及與該延伸方向正交之供給槽2之寬度方向上形成均一。於供給槽2中流動之熔融玻璃之流量係根據基於熔融玻璃之黏度、熔融玻璃之密度、供給槽2中流動之熔融玻璃之自液面至底面2a為止之深度、及底面2a之寬度之算式運算出。藉由對該算式,加上熔融玻璃之流量之線密度於自連接有玻璃供給管106之槽始點側至槽終點側為止之流動方向上成為固定、即溢出量形成均一之條件,而求出供給槽2之底面2a之形狀。又,成形體1之兩端部3a、3b之位置處之供給槽2具有自熔融玻璃溢出至供給槽2之兩側且自上表面3之兩端部3a、3b之位置起與其他部分相同地均一溢出之底面2a至上表面3為止之高度。當熔融玻璃自上表面3之兩端部3a、3b溢出時,熔融玻璃具有自上表面3至熔融玻璃之液面為止之高度。包含將溢出時自底面2a至熔融玻璃之液面為止之高度減去自上表面3至熔融玻璃之液面為止之高度所得之底面2a之形狀之槽曲線與上表面3之交點成為供給槽2之槽終點。藉此,求出連接有玻璃供給管106之供給槽2之自槽始點至槽終點為止之距離,從而決定成形體1之形狀。 冷卻輥8係對平板玻璃SG之寬度方向兩端部進行熱處理之單元。冷卻輥8係相較成形體1之下端4配置於更下游側。又,冷卻輥8係配置於平板玻璃SG之厚度方向兩側,且平板玻璃SG之寬度方向兩側。即,冷卻輥8係於成形體1之正下方對離開成形體1之平板玻璃SG進行熱處理。配置於平板玻璃SG之厚度方向兩側之冷卻輥8係以對狀進行動作。因此,平板玻璃SG之寬度方向兩端部被二對冷卻輥8夾住。冷卻輥8係藉由通向內部之空氣冷卻管進行空氣冷卻。冷卻輥8係接觸於平板玻璃SG之端部SGa,且藉由熱傳導而將平板玻璃SG之端部SGa急冷(端部冷卻步驟)。冷卻輥8係以平板玻璃SG之端部SGa之黏度達到109.0 dPa・s以上之方式,將平板玻璃SG之端部SGa急冷。再者,冷卻輥8較佳為以平板玻璃SG之端部SGa之黏度成為109.0 ~1014.5 dPa・s之範圍內之方式,將平板玻璃SG之端部SGa急冷。 於導件6a、6b各自之附近,以自成形體1之上表面3側延伸至下端4側之方式配置有加熱器,藉由該加熱器而將於一對壁面5向下流動之熔融玻璃中之導件6a、6b附近之部分、及於壁面5向下流動之熔融玻璃進行加熱。該加熱係以於壁面5向下流動之熔融玻璃中之導件6a、6b附近之部分之黏度自成形體1之上表面3至下端4為止(熔融玻璃之該部分自成形體1之上表面3向下流動抵達下端4為止),未達構成該熔融玻璃之玻璃組合物之液相黏度(以下,亦簡稱為「液相黏度」)之方式,沿著導件6a、6b進行。 於使用具備導件之成形體1之溢流下拉法所進行之平板玻璃SG之成形(及將該平板玻璃SG冷卻所得之玻璃基板之製造)中,容易於導件附近、即成形之平板玻璃SG之端部產生失透。該情況被認為因以下原因造成,即,由於以收容成形體1之成形爐於成形體1之下端將熔融玻璃設為適於成形之黏度為目的,而通常設定為不僅以平板玻璃SG之成形為目的而且亦以熔融玻璃之冷卻為目的之溫度、即低於熔融玻璃之溫度,故而,熔融玻璃之熱自導件6a、6b中被奪取,導致導件6a、6b附近之熔融玻璃之溫度容易低於熔融玻璃中之其他部分之溫度;以及,因如此之溫度下降及與導件6a、6b之接觸導致之物理性阻力,導件6a、6b附近之熔融玻璃之向下流動速度容易低於熔融玻璃中之其他部分,從而自與導件6a、6b相接觸起直至離開成形體1為止需要長時間等。 根據日本專利特開2010-215428號公報,存在可抑制於導件之下端產生之失透之可能性。然而,於該文獻之技術中,難以抑制相較導件之下端更上游之區域、尤其熔融玻璃與導件接觸開始冷卻之初期中產生之失透,從而亦無法藉由導件下端之加熱將一次產生之失透消除。又,於將包含適於用於平板顯示器之玻璃基板之無鹼玻璃及含微量鹼玻璃等液相溫度較高且液相黏度較小之玻璃組合物、例如本實施形態之製造方法中使用之液相黏度為80000 dPa・s以上100000 dPa・s以下且液相溫度為1200℃~1220℃之範圍之玻璃組合物之平板玻璃成形之情形時,尤其容易產生如此之失透。 於本實施形態之製造方法中,以於成形體1之壁面5上向下流動之熔融玻璃中之導件6a、6b附近之部分之黏度自成形體1之上表面3至下端4為止保持未達液相黏度之方式(以該部分之溫度自成形體1之上表面3至下端4為止成為液相溫度以上之方式),沿著導件6a、6b加熱熔融玻璃中之該部分。藉此,獲得抑制熔融玻璃之導件附近之部分(熔融玻璃之端部)中之失透之較高效果,從而即便構成熔融玻璃之玻璃組合物具有80000 dPa・s以上100000 dPa・s以下之較小之液相黏度,且具有1200℃~1220℃之範圍之液相溫度之情形時,亦可抑制該端部中之失透之產生。 於本說明書中,所謂液相溫度係指熔融體與結晶之初相之間之平衡溫度,且若超過該溫度則不存在結晶之溫度,所謂液相黏度係指玻璃成為上述液相溫度之黏度。 圖5係表示與成形體1之供給槽2連接之玻璃供給管106之剖面之圖。於玻璃供給管106內,若將於玻璃供給管106之中心區域106a流動之熔融玻璃之溫度與於周邊區域106b流動之熔融玻璃之溫度進行比較,則於中心區域106a流動之熔融玻璃之溫度升高。若於存在中心區域106a與周邊區域106b之溫度差(黏度差)之狀態下,對成形體1之供給槽2供給熔融玻璃,則於設置有成形體1之空間內,熔融玻璃即便被加熱,自玻璃供給管106至成形體1之上表面3為止,熔融玻璃之溫度差亦未被改善,而於殘存熔融玻璃之溫度差之狀態下自成形體1之上表面3朝向下端4溢出。若於成形體1之上表面3溢出之時間點,熔融玻璃中存在溫度差,則熔融玻璃之流動局部地產生變化(停滯),故熔融玻璃未均一地溢出,於成形體1之壁面5向下流動之熔融玻璃之厚度(量)產生變化,於下端4進行成形之平板玻璃SG之厚度局部地產生差異。藉此,於平板玻璃SG中,產生包含條紋之局部性板厚偏差。因平板玻璃之兩端部SGa被冷卻輥8冷卻,且對平板玻璃SG施加朝向兩端部SGa方向之張力,因此,平板玻璃SG中產生之板厚偏差減少。為了利用如此之原理將所產生之平板玻璃SG之板厚偏差抑制為10 μm以下,對成形體1之供給槽2供給時之玻璃供給管106內之熔融玻璃之最大溫度差、及熔融玻璃之黏度變得較為重要。 於本實施形態之製造方法中,自玻璃供給管106供給至成形裝置200(成形體1之供給槽2)時之熔融玻璃之最大溫度差(玻璃供給管106之中心區域106a與周邊區域106b之溫度差)較佳為設為30℃以下,更佳為設為20℃以下,且更佳為設為10℃以下。又,將熔融玻璃之最大黏度差(玻璃供給管106之中心區域106a與周邊區域106b之黏度差)較佳為設為19000 dPa・s以下,更佳為設為12500 dPa・s以下,且更佳為設為6200 dPa・s以下。因將供給至供給槽2之熔融玻璃於設置有成形體1之空間內進行加熱,因此,自成形體1之供給槽2至上表面3為止,熔融玻璃之溫度差變得進一步小於供給槽2之供給時之溫度差,例如成為10℃以下。於如此之溫度差之狀態下,若使熔融玻璃自上表面3溢出,則熔融玻璃均一地溢出,從而於壁面5向下流動之熔融玻璃之厚度(量)形成均一。於下端4匯流而成之熔融玻璃被成形為平板玻璃SG。下端4中之平板玻璃SG之板厚偏差大於10 μm,但藉由以朝向平板玻璃之兩端部SGa施加張力之方式,藉由冷卻輥8將平板玻璃之兩端部SGa冷卻,平板玻璃SG中產生之局部之板厚偏差成為10 μm以下。可藉由冷卻平板玻璃之兩端部SGa而減少之板厚偏差之量對熔融玻璃之黏度產生影響。 於本實施形態之製造方法中,經由玻璃供給管106將熔融玻璃供給至成形裝置200(成形體1之供給槽2)時之熔融玻璃之黏度較佳為22000 dPa・s以上38000 dPa・s以下,更佳為25000 dPa・s以上38000 dPa・s以下,且更佳為25000 dPa・s以上35000 dPa・s以下。若降低對成形體1之供給槽2供給之熔融玻璃之黏度,即,若升高熔融玻璃之溫度,則成形體1之蠕變現象變得顯著,從而亦產生伴隨著自成形開始起時間之經過,平板玻璃之中央部下垂等問題。另一方面,若提昇對成形體1之供給槽2供給之熔融玻璃之黏度,即,若降低熔融玻璃之溫度,則平板玻璃中容易產生板厚偏差,又,容易產生失透。因此,必須將可一面防止板厚偏差及失透之產生一面抑制成形體1之蠕變現象之熔融玻璃供給至成形體1。對成形裝置200供給時之熔融玻璃之黏度較佳為22000 dPa・s以上38000 dPa・s以下。上述黏度係因熔融玻璃之平均黏度而由玻璃組成決定之黏度。以下,將該黏度稱為基於平均黏度之黏度。 於構成熔融玻璃之玻璃組合物之液相黏度為80000 dPa・s以上100000 dPa・s以下之情形時,為了於利用成形體1成形之熔融玻璃之黏度變為最高之成形體1之下端防止失透,而以熔融玻璃之黏度變得未達80000 dPa・s之方式,控制熔融玻璃之黏度。為抑制成形體1之蠕變現象,而以提昇對成形體1之供給槽2供給之熔融玻璃之黏度,同時於成形體1之下端,熔融玻璃之黏度未達80000 dPa・s之方式,將熔融玻璃供給至成形體1之供給槽2。於本實施形態之製造方法中,對成形體1之供給槽2供給之熔融玻璃之黏度(基於平均溫度之黏度)係下限為自22000 dPa・s至25000 dPa・s,且上限為自35000 dPa・s至38000 dPa・s。 因供給至供給槽2中之熔融玻璃之黏度變小,故熔融玻璃自供給至供給槽2起至自上表面3溢出為止之時間變短。因此,於該時間之期間,熔融玻璃受到之熱量減少。熔融玻璃係以供給槽2內,溫度差變小之方式進行加熱,但若自供給至溢出為止之時間較短,則無法消除溫度差,從而於存在溫度差之狀態下溢出。如此一來,產生向下流動之速度局部出現變化之部位,從而成為板厚偏差之原因。藉由將對成形體1之供給槽2供給之熔融玻璃之黏度(基於平均溫度之黏度)設為22000 dPa・s至38000 dPa・s,於成形體1之下端4匯流而成形之平板玻璃SG成為低黏度,容易受到冷卻輥8之冷卻效應,而被拉拔至寬度方向之端部側,從而平板玻璃SG之板厚偏差之抑制效果變大。另一方面,若熔融玻璃成為低黏度,則至溢出為止之時間變短,故若存在熔融玻璃之溫度差(黏性差),則因該溫度差(黏性差)而產生板厚偏差。因此,將供給至供給槽2之熔融玻璃之最大溫度差設為30℃以下。可藉由將滿足該等2個條件之熔融玻璃供給至供給槽2,而使平板玻璃SG之板厚偏差成為10 μm以下。 為了將供給至供給槽2之熔融玻璃之最大溫度差設為30℃以下,玻璃供給管106中流動之熔融玻璃之溫度管理較為重要,且於玻璃供給管106之管之長邊方向上,如圖6所示地劃分為複數個區SC1~SC9及複數個管區段PP1~PP3,進行溫度之調整。圖6係表示玻璃供給管106之管之長邊方向上之於玻璃供給管106之中流動之熔融玻璃之溫度變化之圖表。於圖6中,實線L1係表示作為與玻璃供給管106之內周面接觸之熔融玻璃之溫度、即玻璃供給管106之溫度之「管溫度」之變化,虛線L2係表示作為玻璃供給管106之剖面中心之熔融玻璃之溫度之「中心溫度」之變化。於圖6中,鏈線L3係表示以每一單位剖面面積中之熔融玻璃之質量流量進行加權平均所得之玻璃平均溫度。使用該平均溫度,求出熔融玻璃之基於平均溫度之黏度。 對於圖6所示之熔融玻璃之溫度變化進行說明,流入至玻璃供給管106中之熔融玻璃係均質化步驟ST3中均質化所得之熔融玻璃,因此,流入第1管區段PP1(區SC1~SC5)中之熔融玻璃之管溫度與中心溫度之差為零。第1管區段PP1係用以將熔融玻璃冷卻至不低於玻璃之失透溫度之程度之區域。於第1管區段PP1中,存在管溫度及中心溫度逐漸地下降,且因來自玻璃供給管106之散熱,管溫度與中心溫度之差逐漸地增加之傾向。於第1管區段PP1與第2管區段PP2之交界處,管溫度與中心溫度之差較佳為100℃以下。於圖6中,於第1管區段PP1中,玻璃平均溫度自1470℃下降至1260℃。 於第2管區段PP2中,管溫度之下降得到抑制。第2管區段PP2中流動之電流高於第1管區段PP1中流動之電流。因此,利用通電加熱賦予至第2管區段PP2之熱量大於利用通電加熱賦予至第1管區段PP1之熱量。因此,於第2管區段PP2中,來自玻璃供給管106之散熱得到抑制,玻璃供給管106之溫度維持大致固定。此時,於第2管區段PP2內,熱自玻璃供給管106之剖面中心之熔融玻璃朝向與玻璃供給管106之內周面接觸之熔融玻璃傳遞,故中心溫度逐漸地下降。其結果,於第2管區段PP2中,存在管溫度與中心溫度之差逐漸地減少之傾向。於第2管區段PP2與第3管區段PP3之交界處,管溫度與中心溫度之差較佳為50℃以下。於圖6中,於第2管區段PP2中,玻璃平均溫度自1260℃下降至1250℃。 再者,於第2管區段PP2之第7區SC7中,玻璃供給管106之內徑減少。因此,於第2管區段PP2中,玻璃供給管106之外周面之面積逐漸地減少,因此,經由玻璃供給管106之熔融玻璃之散熱被抑制。即,於第2管區段PP2中,因高電流之賦予與內徑減少此2個主要因素,管溫度與中心溫度之差逐漸地減少。 於第3管區段PP3中,熔融玻璃之管溫度與中心溫度之最大溫度差達到30℃以下。將第3管區段PP3包圍之耐火材料之隔熱性能優於將第1管區段PP1及第2管區段PP2包圍之耐火材料106。因此,第3管區段PP3係與第1管區段PP1及第2管區段PP2相比,經由玻璃供給管106之熔融玻璃之散熱進一步被抑制。又,第3管區段PP3中流動之電流低於第2管區段PP2中流動之電流,且利用通電加熱賦予至第3管區段PP3之熱量小於利用通電加熱賦予至第2管區段PP2之熱量。因此,第3管區段PP3之中流動之熔融玻璃之溫度上升得到抑制。藉此,於第3管區段PP3中,在玻璃平均溫度成為大致一定之狀態下,因熔融玻璃內之熱傳遞,管溫度與中心溫度之差進一步減少。圖6中,於第3管區段PP3中,玻璃平均溫度維持1250℃。 再者,通過玻璃供給管106之熔融玻璃之溫度之較佳範圍係如下上述。於玻璃供給管106之上游側之端部,管溫度及中心溫度較佳為1420℃~1470℃。於第1管區段PP1與第2管區段PP2之交界處,較佳為,管溫度為1210℃~1260℃,且中心溫度為1300℃~1350℃。於第2管區段PP2與第3管區段PP3之交界處,較佳為,管溫度為1210℃~1260℃,且中心溫度為1250℃~1300℃。於玻璃供給管106之下游側之端部,管溫度及中心溫度較佳為1235℃~1265℃。 藉由如此之玻璃供給管106所進行之熔融玻璃之溫度調整,而將供給至供給槽2之熔融玻璃之最大溫度差設為30℃以下。 再者,熔融玻璃之中心溫度之測定因存在難以使用溫度計之情形,故於該情形時,可使用自玻璃供給管106起之單位時間、單位面積之散熱量之資訊、玻璃供給管106之單位時間、單位面積之加熱量之資訊、流入至玻璃供給管106時之熔融玻璃之溫度及流量之資訊,根據玻璃供給管106之管溫度之測定結果,藉由電腦模擬而求出。 再者,上述管溫度係利用安裝於玻璃供給管106之各位置處之溫度計(未圖示)進行測定。黏度係藉由安裝於玻璃供給管106與成形體1之供給槽2連接之部分之黏度計(未圖示)進行測定。黏度計係使用例如細管式黏度計或旋轉式黏度計。細管式黏度計係使測定對象之熔融玻璃通過細管,根據熔融玻璃通過細管之時間(流量)及細管之兩端之壓力差,測定熔融玻璃之黏度。旋轉式黏度計係藉由根據旋轉體之轉矩等讀取熔融玻璃自旋轉體受到之阻力即黏性阻力而測定熔融玻璃之黏度。 於本實施形態之製造方法中,較佳為以於成形體1之壁面5向下流動之熔融玻璃中之導件6a、6b附近之部分之溫度成為自成形體1之上表面3至下端4為止相較液相溫度高10℃以上之溫度之方式,加熱該部分,更佳為以成為相較液相溫度高15℃以上之溫度之方式加熱該部分。於該等情形時,成形之平板玻璃之端部中失透之產生被更確實地抑制。具體之液相溫度係因玻璃組合物之組成而異。 本實施形態之製造方法較佳為於成形步驟中,以於成形體1之壁面5向下流動之熔融玻璃中之導件6a、6b附近之部分之溫度成為自成形體1之上表面3至下端4為止相較液相溫度高10℃~150℃之方式(以成為相較液相溫度高10℃以上,且將液相溫度加上150℃所得之溫度以下之方式),沿著導件加熱該部分。藉此,可抑制成形體1之變形、及成形後之平板玻璃SG中之寬度方向之收縮。進而較佳為以於成形體1之壁面5向下流動之熔融玻璃中之導件6a、6b附近之部分之溫度成為自成形體1之上表面3至下端4為止相較液相溫度高15℃~100℃之方式,沿著導件加熱該部分。 藉由與熔融玻璃離開成形體1後之端部之急冷(平板玻璃SG之端部SGa之急冷)進行組合,平板玻璃SG之板厚偏差達到10 μm以下。又,該端部SGa中失透之產生進而被確實地抑制。 即便以於成形體1之壁面5向下流動之熔融玻璃中之導件6a、6b附近之部分之溫度自成形體1之上表面3至下端4為止充分地高於液相溫度之方式,使於成形體1向下流動之熔融玻璃整體之溫度相較液相溫度充分地成為高溫,理論上亦可抑制失透。然而,於製造液相溫度較高之玻璃之情形時,現實中,溢流下拉法中無法適用如此之方法。其原因在於,存在適合溢流下拉法所進行之平板玻璃成形之熔融玻璃之黏度(為避免產生下述平板玻璃之鬆弛或平板玻璃之寬度收縮之問題,成形體1之下端4中之熔融玻璃之黏度較佳為40000 dPa・s以上,更佳為70000 dPa・s以上)。若以熔融玻璃中之導件附近之部分之溫度變得充分地高於液相溫度之方式,使於成形體1向下流動之熔融玻璃整體之溫度相較液相溫度充分地成為高溫,或於成形體1之下端4過度地進行加熱,則存在導致成形體1之下端4中之熔融玻璃之黏度變得小於上述適當之範圍之可能性。如此一來,產生如下問題,即,離開成形體1後之平板玻璃之黏度未能充分地上升,平板玻璃以配置於成形體1之下游側之搬送輥之拉伸速度以上之速度落下,導致平板玻璃於該輥上鬆弛,或平板玻璃之寬度收縮。又,成形體之溫度越高,則伴隨成形體之使用而經時變化之蠕變現象變得越顯著,從而亦產生平板玻璃之中央部伴隨著自成形開始起之時間經過而下垂等問題。若考慮作為玻璃基板所需之厚度及成形後之緩冷步驟中實施之平板玻璃之溫度控制,則搬送輥之拉伸速度之增加存在極限(若考慮緩冷步驟中實施之平板玻璃之溫度控制,則平板玻璃之搬送速度較佳為50~500 m/小時,較佳為100~400 m/小時,且較佳為120~300 m/小時)。 又,若使熔融玻璃中之導件附近之部分之溫度充分地高於液相溫度,則進行成形之平板玻璃之寬度收縮,從而無法確保作為玻璃基板之產品寬度。又,若使於成形體1向下流動之熔融玻璃整體之溫度相較液相溫度充分地成為高溫,則產生成形體1之蠕變現象,且若該蠕變現象變得顯著,則製造之玻璃基板之板厚均一性下降。 自成形體1中之熔融玻璃所流動之壁面突出之導件之高度較佳為低至成形裝置之下方之位置之程度。較佳為成形體1之下端4為兩側之傾斜壁面彼此連接而成之直線狀棱線,且一對導件於傾斜之壁面中之高度在該棱線之位置處為0(零)。藉此,可進一步抑制平板玻璃之端部(耳部)二叉狀打開,從而可更穩定地連續生產玻璃基板。 冷卻輥8之冷卻量及旋轉量係由控制裝置(未圖示)進行控制。控制裝置係主要包括CPU、RAM、ROM及硬碟等之電腦。控制裝置可控制使冷卻輥8驅動之驅動馬達,獲取及調節夾持平板玻璃SG之寬度方向之端部SGa之一對冷卻輥8與平板玻璃SG之間之接觸負載。控制裝置係分別單獨地控制各冷卻輥8之冷卻量。進而,控制裝置為了將下述說明之平板玻璃SG之厚度方向之剖面形狀成為目標形狀作為目的,利用冷卻輥8之冷卻控制對平板玻璃SG施加之張力,而至少將作為搬送部、獲取部、判定部及控制部發揮作用之4個程式記憶執行。 搬送部係使用設置於成形體1之下方之搬送輥,將藉由成形體1成形所得之平板玻璃SG於緩冷空間中以特定之搬送速度搬送至下方。搬送部控制使搬送輥驅動之驅動馬達,調節搬送輥之旋轉速度,藉此,調節平板玻璃SG之搬送速度。 獲取部係藉由利用電腦模擬求出成形體1之形狀之時間變化,而獲取與成形體1之當前形狀相關之形狀資料。具體而言,獲取部基於蠕變特性參數獲取形狀資料。蠕變特性參數係用以再現施加至成形體1之應力、成形體1之溫度、及因蠕變變形產生之成形體1之應變速度之間之關係之參數。此處,施加至成形體1之應力係沿著成形體1之長邊方向(供給槽2之延伸方向)壓縮成形體1之力。又,成形體1之應變速度假設為不隨時間變化而固定。最初,獲取部測定施加至成形體1之應力固定之條件下成形體1之應變速度對於成形體1之溫度依存變化。繼而,獲取部測定成形體1之溫度固定之條件下成形體1之應變速度對於施加至成形體1之應力之應力依存變化。繼而,獲取部決定可將成形體1之應變速度之溫度依存變化及應力依存變化之測定值再現之蠕變特性參數。繼而,獲取部藉由電腦模擬,使用所決定之蠕變特性參數,運算特定之溫度及應力下之成形體1之應變速度,求出成形體1之形狀之時間變化,藉此,獲取成形體1之形狀資料。圖7係藉由獲取部獲取之成形體1之形狀資料之一例。圖7表示沿著與藉由成形體1成形所得之平板玻璃SG之表面垂直之方向觀察所得之成形體1。圖7中,相較實際情況強化地表示成形體1之蠕變變形。於圖7中,以虛線表示未使用之成形體1之形狀、即蠕變變形之前之成形體1之形狀,且以實線表示蠕變變形之後之成形體1之當前形狀。 獲取部係根據成形體1之基於蠕變變形之形狀資料,至少獲取成形體1之上表面3之鉛垂方向之位移量即上表面位移量。於圖7中,上表面位移量係蠕變變形前之上表面3與蠕變變形後之上表面3之間之鉛垂方向之尺寸。再者,於圖7中,表示成形體1之長邊方向上之上表面位移量之最大值即最大上表面位移量L。又,獲取部獲取藉由玻璃基板形狀測定裝置(未圖示)測定所得之玻璃基板之厚度資料。厚度資料係例如利用成形裝置200製造之玻璃基板之厚度之寬度方向之分佈。 判定部係判定由獲取部獲取之位移量L是否達到基準量。此處,所謂基準量係指當對平板玻璃SG施加固定之張力(初始之張力),將平板玻璃SG(玻璃基板)成形為成形預定之厚度(例如0.1 mm~0.8 mm)時,板厚偏差可滿足±10 μm之量。於未使施加至平板玻璃SG之張力自初始值變化之情形時,若位移量L超過基準量,則平板玻璃SG之板厚偏差超過±10 μm。因此,藉由使施加至平板玻璃SG之張力相較初始張力增大,而以平板玻璃SG之板厚偏差成為±10 μm以內之方式控制平板玻璃SG之厚度。基準量可因初始張力、平板玻璃SG之成形預定之板厚、及板厚偏差等而任意地變更,例如為3 mm~30 mm。 控制部係將成形體1未沿著成形所得之平板玻璃SG之寬度方向(成形體1之長邊方向)移位時所施加且平板玻璃SG之厚度方向之剖面形狀成為目標形狀之張力設為基準張力(初始張力),且以藉由控制冷卻輥8之冷卻量而將平板玻璃SG之寬度方向之兩端部SGa冷卻,藉此,施加至平板玻璃SG之張力成為基準張力之方式進行控制。於成形體1未移位之狀態下,藉由於平板玻璃SG之寬度方向上施加基準張力,平板玻璃SG成為成形預定之板厚,從而板厚偏差滿足±10 μm。若於成形體1蠕變變形之狀態下,施加至平板玻璃SG之張力一直為基準張力,則無法成為目標形狀,例如無法成形為成形預定之板厚,且,板厚偏差無法滿足±10 μm。因此,控制部不僅施加基準張力,而且對平板玻璃SG施加與成形體1之位移相應之張力。此處,成形體1之位移係例如成形體1之長邊方向上之上表面位移。控制部係基於由獲取部獲取之成形體1之形狀資料,以平板玻璃SG之厚度成為成形預定之厚度之方式,又,以平板玻璃SG之寬度方向之板厚偏差變小之方式,控制冷卻輥8之冷卻量,藉此,控制對平板玻璃SG施加之張力。成形體1之形狀資料係例如成形體1之長邊方向上之上表面位移量之分佈即形狀分佈。控制部以根據形狀分佈求得之上表面3之位移量越大,則朝向平板玻璃SG之寬度方向之張力變得越大之方式,控制冷卻輥8之冷卻量。作為根據形狀分佈求得之上表面3之位移量,例如使用最大上表面位移量L。 於成形體1之下端4成形之平板玻璃SG於離開下端4後,因自身之表面張力,中央區域SGb開始朝向寬度方向之中央收縮。因此,冷卻輥8將平板玻璃SG之兩端部SGa冷卻使兩端部SGa之黏度上升,以張力自中央區域SGb朝向兩端部SGa施加之方式抑制平板玻璃SG於寬度方向上收縮,以使平板玻璃SG之中央區域SGb之厚度形成均一。然而,若成形體1進行蠕變變形,則平板玻璃SG之中央區域SGb附近之熔融玻璃量增多,中央區域SGb之厚度產生變化。即,平板玻璃SG之厚度方向之剖面形狀不再為目標形狀。圖8係表示因成形體1之蠕變變形,中央區域SGb附近之厚度增加之平板玻璃SG之圖。若成形體1進行蠕變變形,則自上表面3之端部3a與端部3b之間溢出之熔融玻璃之量增多,故平板玻璃SG之中央區域SGb附近之厚度增加。於圖8中,中央區域SGb附近之厚度相比成形預定之厚度最多變厚D1,從而中央區域SGb之厚度成為不均一。因此,控制部根據成形體1之形狀資料,使冷卻輥8之冷卻量變化,以自平板玻璃SG之中央區域SGb朝向兩端部SGa施加張力之方式抑制平板玻璃SG於寬度方向上收縮,以使平板玻璃SG之中央區域SGb之厚度形成均一。 圖9係表示成形體1之最大上表面位移量L與施加至平板玻璃SG之張力T之關係之圖。於圖9中,將最大上表面位移量L記作位移量L。控制部設為於利用判定部判定成形體1之最大上表面位移量L未超過L1之情形時,可忽視成形體1之蠕變變形造成之平板玻璃SG之中央區域SGb之厚度變化,不使施加至平板玻璃SG之張力T自初始值T1(位移量L之範圍:0以上未達L1)進行變化。若成形體1之位移量L未達L1,則控制部不使冷卻輥8之冷卻量產生變化,以初始值T1維持張力T,藉此,成形之平板玻璃SG之板厚偏差滿足±10 μm。控制部設為於利用判定部判定成形體1之位移量L超過L1之情形時,如圖9所示,以與最大上表面位移量L對應之張力T施加至平板玻璃SG之方式進行控制。若最大上表面位移量L達到L1以上,則如圖8所示,平板玻璃SG之中央區域SGb之厚度增加,厚度不再形成均一。因此,控制部以如下方式進行控制:以與位移量L對應之方式,將大於初始值T1之張力T=T1+A×最大上表面位移量L(位移量L之範圍:L1以上未達Lm,A:係數)自平板玻璃SG之中央區域SGb朝向兩端部SGa施加至平板玻璃SG。控制部係成形體1之變形愈大則愈增強兩端部SGa之冷卻。具體而言,使冷卻輥8之冷卻量增加,從而使兩端部SGa之黏度上升。若兩端部SGa之黏度變高,則自中央區域SGb朝向兩端部SGa之張力T變大,將位於平板玻璃SG之中央區域SGb之熔融玻璃向兩端部SGa拉伸,從而中央區域SGb之厚度接近於成形預定之厚度,厚度形成均一。控制部係以使兩端部SGa之黏度自例如109.0 dPa・s增加至1014.5 dPa・s為止,藉此張力T變大之方式進行控制。 再者,於最大上表面位移量L之範圍為L1以上未達Lm之情形時,藉由將張力T控制為T1至Tm,中央區域SGb之厚度向成形預定之厚度接近,從而厚度形成均一,但於位移量L超過Lm進行移位之情形時,僅控制張力T,則難以一面使中央區域SGb之厚度向成形預定之厚度接近,一面使厚度形成均一,因此,藉由判定部而判定已到達成形體1之定期更換時期。 又,因成形體1之蠕變變形,平板玻璃SG之局部之板厚偏差(表面凹凸差)亦產生變化。平板玻璃SG之體積收縮量係伴隨著自平板玻璃SG之端部SGa朝向中央區域SGb而變大,因此,於平板玻璃SG之中央區域SGb,拉伸應力進行作用。因中央區域SGb附近之厚度變厚,自兩端部SGa朝向中央區域SGb之張力變大,故平板玻璃SG之表面凹凸差變大。圖10(a)係將圖4之A-A線之剖面放大所得之圖,圖10(b)係將圖4之B-B線之剖面放大所得之圖。於藉由冷卻輥8對平板玻璃SG施加張力T之前,平板玻璃SG朝向中央區域SGb收縮,因此,平板玻璃SG之表面凹凸差成為D2,於藉由冷卻輥8對平板玻璃SG施加張力T之後,平板玻璃SG之表面凹凸差成為小於D2之D3。若成形體1進行蠕變變形,則平板玻璃SG之表面凹凸差D2、D3亦變大。因此,藉由以對應於最大上表面位移量L之方式,施加自中央區域SGb朝向兩端部SGa之張力T,而將平板玻璃SG向兩端部SGa拉伸,故平板玻璃SG之表面凹凸差D3變小。為使中央區域SGb之厚度接近成形預定之厚度,而藉由以對應於最大上表面位移量L之方式施加張力T,使得平板玻璃SG之表面凹凸差D3變小,從而平板玻璃SG之中央區域SGb之厚度形成均一。 又,控制部亦可藉由對平板玻璃SG施加張力T,而抑制存在產生於平板玻璃SG之搬送方向上之可能性之條紋。條紋係於特定之寬度範圍中平板玻璃SG之厚度(高度)變動所致之應變之一種,且於平板玻璃SG之搬送方向上紋路狀地連續產生。又,條紋之主要因素中亦包括玻璃之黏度差。若藉由控制部控制冷卻輥8之冷卻量而於平板玻璃SG之寬度方向上施加張力,則平板玻璃SG之表面凹凸之一種即局部地產生之條紋被拉伸至平板玻璃SG之兩端側SGa,從而成形表面凹凸差變小且局部之板厚偏差滿足±10 μm之平板玻璃SG。 如以上所說明,可藉由於成形體1之下端4,使對平板玻璃SG施加之平板玻璃SG之寬度方向之張力T對應於成形體1之蠕變變形引起之位移量進行變化,而一面使中央區域SGb之厚度接近成形預定之厚度,一面使厚度形成均一。於因成形體1之蠕變變形,成形體1之長邊方向之中央部向下方下垂而撓曲之情形時,可藉由將冷卻輥8之冷卻量增大,使對平板玻璃SG施加之平板玻璃SG之寬度方向之張力T變大,而降低平板玻璃SG之寬度方向之板厚偏差。其結果,可降低作為最終產品之玻璃基板之板厚偏差。 又,於使用液相溫度較高之玻璃及應變點較高之玻璃之玻璃基板之製造步驟中,成形體1之蠕變變形因成形體1之溫度容易增高而尤其容易成為問題。又,近年來,因玻璃基板不斷大型化,成形體之長邊方向之尺寸不斷變長,因此,存在蠕變變形造成之成形體1之撓曲變得更顯著之傾向。於本實施形態中,可藉由調節冷卻輥8之冷卻量,使對平板玻璃SG施加之張力T變化,而有效地降低因成形體1之蠕變變形引起之平板玻璃SG之寬度方向之板厚偏差。 根據本實施形態之製造方法,即便於構成熔融玻璃之玻璃組合物之液相溫度較高,且液相黏度較小之情形時,例如玻璃組合物為無鹼玻璃、含微量鹼玻璃等情形時,亦可獲得抑制成形之平板玻璃之端部中之失透之效果。即,於構成熔融玻璃之玻璃組合物之液相溫度較高且液相黏度較小之情形時,藉由本實施形態之製造方法而獲得之優點較大。 於本實施形態之製造方法中,構成熔融玻璃之玻璃組合物之液相黏度為10000 dPa・s以下。如此之玻璃組合物先前於溢流下拉法之平板玻璃之成形中容易產生端部中之失透問題。然而,於本實施形態之製造方法中,可獲得抑制失透之效果。 本實施形態之製造方法中所用之熔融玻璃之液相黏度為100000 dPa・s以下。液相黏度為100000 dPa・s以下之玻璃組合物中,上述失透之問題變得更顯著,但本實施形態之製造方法獲得了抑制失透之效果。根據可穩定地實施溢流下拉法之平板玻璃之成形之觀點,液相黏度較佳為80000 dPa・s以上。 構成本實施形態之製造方法中所用之熔融玻璃之玻璃組合物之液相溫度較佳為1200℃以上1220℃以下。如此之玻璃組合物先前於溢流下拉法之平板玻璃之成形中容易產生端部中之失透問題。然而,本實施形態之製造方法獲得了抑制失透之效果。 於本實施形態之製造方法中,熔融玻璃亦可含有氧化鋯及/或氧化錫。於含有氧化鋯之熔融玻璃中,與不含氧化鋯之情形相比,玻璃組合物之液相溫度上升。如此之熔融玻璃先前於溢流下拉法之平板玻璃之成形中容易產生端部中之失透問題。然而,本實施形態之製造方法獲得了抑制失透之效果。氧化鋯即便於作為玻璃組合物之成分原本包含於熔融玻璃之情形以外,亦可藉由採用使用高氧化鋯系耐火材料所構成之溶解槽及成形裝置而於熔融玻璃中溶出。尤其,於使用如此之溶解槽,將玻璃原料電解溶解之情形時,存在熔融玻璃中之氧化鋯濃度變高之傾向。即,本實施形態之製造方法更適合於採用使用高氧化鋯系耐火材料所構成之溶解槽將玻璃原料電解溶解之情形。 再者,使用高氧化鋯系耐火材料所構成之溶解槽與先前廣泛使用之氧化鋁電鑄耐火材料所構成之溶解槽相比,不易被玻璃腐蝕,從而作為溶解槽之使用壽命較長。又,亦可抑制熔融玻璃之發泡。因此,適於形成熔融溫度(玻璃組合物之黏度達到102.5 泊之溫度)較高之玻璃組合物例如無鹼玻璃及含微量鹼玻璃之熔融玻璃。 又,於利用溶解槽形成之熔融玻璃包含無鹼玻璃或含微量鹼玻璃之情形時,玻璃組合物之電阻率容易變高,從而存在電流流入高氧化鋯耐火材料中而不流入玻璃原料中之傾向。若電流流入該耐火材料中,則氧化鋯於利用溶解槽形成之熔融玻璃中溶出。即,本實施形態之製造方法進而適合於採用使用高氧化鋯系耐火材料所構成之溶解槽,藉由電解溶解而形成無鹼玻璃或含微量鹼玻璃之熔融玻璃之情形。 液晶顯示器、有機EL顯示器等之FPD(Flat Panel Display,平板顯示器)用玻璃基板中,較佳為包含無鹼玻璃或含微量鹼玻璃之玻璃基板。其原因在於,若於面板製造步驟中鹼成分自玻璃基板溶出,則存在薄膜電晶體(TFT,Thin-film transistor)等電子元件之特性劣化之虞。即,本實施形態之製造方法尤其適合於採用使用高氧化鋯系耐火材料所構成之溶解槽將玻璃原料電解溶解,且使用所得之熔融玻璃藉由溢流下拉法製造平板顯示器用玻璃基板之情形。再者,所謂無鹼玻璃係指實質上不含鹼金屬氧化物(就含有率而言未達0.05質量%)之玻璃組合物。所謂含微量鹼玻璃係指含有0.05~2.0質量%之鹼金屬氧化物之玻璃組合物。 含有氧化錫之熔融玻璃中,容易因氧化錫結晶化而產生失透。又,於與氧化鋯共存之情形時,氧化錫具有使氧化鋯結晶化之作用。如此之熔融玻璃於先前利用溢流下拉法成形平板玻璃之過程中尤其容易產生端部中之失透問題。然而,本實施形態之製造方法獲得了抑制失透之效果。 於本實施形態之製造方法中,構成熔融玻璃之玻璃組合物亦可為無鹼玻璃或含微量鹼玻璃。與含有超過2.0質量%之鹼金屬氧化物之鹼玻璃相比,如此之無鹼玻璃或含微量鹼玻璃存在液相溫度較高且液相黏度較小之傾向,但本實施形態之製造方法獲得了抑制失透之效果。該效果如上所述於採用使用高氧化鋯系耐火材料所構成之溶解槽藉由電解溶解形成無鹼玻璃或含微量鹼玻璃之熔融玻璃之情形時變得尤其顯著。 再者,根據防止TFT(Thin Film Transistor)等電子元件之特性劣化之觀點,無鹼玻璃適合平板顯示器用玻璃基板。其中,根據溶解性及澄清性之觀點,含微量鹼玻璃適合平板顯示器用玻璃基板。藉由特意微量地含有鹼金屬氧化物製成含微量鹼玻璃,使得玻璃組合物之溶解性及澄清性提昇。因鹼金屬氧化物之存在,玻璃之鹼性度上升,從而價數變動之金屬變得容易氧化係有助於澄清性。又,即便於使用高氧化鋯系耐火材料所構成之溶解槽中藉由玻璃原料之電解溶解而形成熔融玻璃之情形時,亦可使玻璃之電阻率小於無鹼玻璃,故能夠抑制氧化鋯向熔融玻璃之溶出,從而抑制熔融玻璃之失透性上升。 於本實施形態之製造方法中,就構成熔融玻璃之玻璃組合物而言,呈現102.5 泊之黏度之溫度(熔融溫度)亦可為1500℃~1750℃。如此之玻璃組合物於熔融時需要高溫,因此,於藉由使用高氧化鋯系耐火材料所構成之溶解槽形成熔融玻璃之情形時,氧化鋯容易溶出。即便對於如此之玻璃組合物,本實施形態之製造方法亦獲得了抑制失透之效果。 作為利用本實施形態之製造方法製造之玻璃基板中所含之玻璃成分,例如可列舉SiO2 、Al2 O3 、B2 O3 、MgO、CaO、SrO、BaO、Li2 O、Na2 O、K2 O、ZrO2 、TiO2 、ZnO、及P2 O5 。 SiO2 係玻璃之骨架成分,故為必要成分。若含量變少,則存在應變點降低,熱膨脹係數增加之傾向。又,若SiO2 含量過少,則難以使玻璃基板實現低密度化。另一方面,若SiO2 含量過多,則存在熔融玻璃MG之電阻率上升,熔融溫度顯著變高從而難以溶解之傾向。若SiO2 含量過多,則亦存在失透溫度上升,抗失透性降低之傾向。進而,若SiO2 含量過多,則蝕刻速率變慢。根據如此之觀點,SiO2 之含量較佳為例如60~80mol%之範圍。SiO2 之含量更佳為64~73mol%或65~75mol%,進一步更佳為66~72mol%,進而更佳為67~71mol%之範圍。 Al2 O3 係提昇應變點之必要成分。若Al2 O3 含量過少,則應變點降低。進而,若Al2 O3 含量過少,則存在楊氏模數及氧所進行之蝕刻速率亦降低之傾向。另一方面,若Al2 O3 含量過多,則玻璃之失透溫度上升,抗失透性下降,故存在成形性惡化之傾向。根據如此之觀點,Al2 O3 之含量為8~20mol%之範圍。Al2 O3 之含量較佳為10~17mol%,更佳為10.5~17mol%,更佳為11~15mol%,進而較佳為12~15mol%之範圍。 B2 O3 係使玻璃之高溫黏性降低,改善熔融性之成分。即,因使熔融溫度附近之黏性降低,故改善溶解性。又,B2 O3 亦係使失透溫度降低之成分。若B2 O3 含量較少,則存在溶解性及抗失透性下降之傾向。若B2 O3 含量過多,則應變點及楊氏模數下降。又,因玻璃成形時B2 O3 之揮發,導致容易產生失透。尤其,應變點較高之玻璃因存在成型溫度變高之傾向,故促進上述揮發,從而失透之產生成為顯著之問題。又,因玻璃溶解時B2 O3 之揮發,玻璃之非均質變得顯著,變得容易產生條紋。根據如此之觀點,B2 O3 含量為0~15mol%,較佳為0~8mol%,更佳為0~7mol%,進而較佳為0.1~6mol%,更加較佳為1~5mol%,進一步更佳為1.5~4.5mol%之範圍。 MgO係使溶解性提昇之成分。又,MgO係鹼土類金屬之中使密度難以增加之成分,因此,若使該含量相對地增加,則容易實現低密度化。可藉由含有MgO,而降低熔融玻璃MG之電阻率及熔融溫度。其中,若MgO之含量過多,則玻璃之失透溫度急劇上升,故尤其於成形步驟中容易出現失透。根據如此之觀點,MgO含量為0~15mol%,較佳為1~15mol%,更佳為0~6mol%,進而較佳為1~6mol%之範圍。或者,MgO含量較佳為0~15mol%,更佳為0~6mol%,進而較佳為1~6mol%之範圍。 CaO係對於不使玻璃之失透溫度急劇地上升且提昇玻璃之溶解性有效之成分。又,CaO係鹼土類金屬氧化物之中使密度難以增加之成分,故若使該含量相對地增加,則容易實現低密度化。若含量過少,則存在產生熔融玻璃MG之電阻率上升及抗失透性下降之傾向。若CaO含量過多,則存在熱膨脹係數增加,密度上升之傾向。根據如此之觀點,CaO含量為0~20mol%,較佳為1~15mol%,更佳為2~11mol%,進而較佳為4~9mol%之範圍。 SrO係能夠降低玻璃之失透溫度之成分。SrO雖非必須,但若含有SrO,則抗失透性及溶解性提昇。然而,若SrO含量過多,則導致密度上升。根據如此之觀點,SrO含量為0~15mol%,較佳為0~8mol%,更佳為0~3mol%,進而較佳為0~1mol%,更加較佳為0~0.5mol%之範圍,進一步更佳為實質上不含有。 BaO係能夠使玻璃之失透溫度及熔融玻璃MG之電阻率有效地下降之必要成分。若含有BaO,則抗失透性及溶解性提昇。然而,若BaO之含量過多,則導致密度上升。又,因環境負荷之觀點、及存在熱膨脹係數增大之傾向,故BaO含量為0~15mol%或0.1~15mol%,較佳為1~15mol%,更佳為1~10mol%,進而較佳為1.5~6mol%之範圍。 Li2 O及Na2 O係存在增大玻璃之熱膨脹係數導致熱處理時使基板破損之虞之成分。又,Li2 O及Na2 O亦係使應變點降低之成分。另一方面,因可使熔融玻璃MG之電阻率降低,故可藉由含有Li2 O及Na2 O而抑制溶解槽被侵蝕。根據以上之觀點,Li2 O之含量較佳為0~0.5mol%,更佳為實質上不含有。Na2 O之含量較佳為0~0.5mol%,更佳為0~0.2mol%。再者,Na2 O係與Li2 O相比使應變點更難以降低之成分,故較佳為Na2 O>Li2 O。再者,根據防止自玻璃基板溶出導致TFT特性劣化之觀點,Li2 O及Na2 O較佳為實質上不含有。 K2 O係提昇玻璃之鹼性度促進澄清性之成分。又,K2 O係使熔融玻璃MG之電阻率降低之成分。若含有K2 O,則熔融玻璃MG之電阻率下降,故可防止電流流入至構成溶解槽之耐火材料,從而可抑制溶解槽被侵蝕。又,於構成溶解槽之耐火材料含有氧化鋯之情形時,可抑制溶解槽被侵蝕,從而氧化鋯自溶解槽向熔融玻璃MG溶出,因此,亦可抑制氧化鋯引起之失透。又,因可使溶解溫度附近之玻璃黏性降低,故溶解性與澄清性提昇。另一方面,若K2 O含量過多,則存在熱膨脹係數增大及應變點降低之傾向。根據如此之觀點,K2 O含量較佳為0~0.8mol%,更佳為0.01~0.5mol%,進而較佳為0.1~0.3mol%之範圍。 ZrO2 及TiO2 係使玻璃之應變點提昇之成分。然而,若ZrO2 量及TiO2 量過多,則失透溫度顯著地上升,故存在抗失透性降低之傾向。尤其,ZrO2 因熔點高導致難熔,而引發原料之一部分沈積於溶解槽之底部之類之問題。若該等未溶解之成分混入至玻璃坯體,則作為內含物而引起玻璃之品質惡化。又,TiO2 係使玻璃著色之成分,故對於顯示器用基板較為欠佳。根據如此之觀點,於本實施形態之玻璃基板中,ZrO2 及TiO2 之含量較佳為分別為0~5mol%,更佳為0~2mol%之範圍,進而較佳為實質上不含有。 ZnO係使溶解性提昇之成分。但並非必要成分。若ZnO含量過多,則存在失透溫度上升,應變點降低,且密度上升之傾向。根據如此之觀點,ZnO含量較佳為0~5mol%,更佳為0~2mol%之範圍,進而較佳為實質上不含有。 P2 O5 係使高溫黏性降低,使溶解性提昇之成分。但並非必要成分。若P2 O5 含量過多則應變點降低。又,因玻璃溶解時P2 O5 之揮發,而導致玻璃之非均質變得顯著,容易產生條紋。根據如此之觀點,P2 O5 含量較佳為0~3mol%,更佳為0~1mol%,進而較佳為0~0.5mol%之範圍,更加較佳為實質上不含有。 適用本實施形態之玻璃基板包含例如含有以下組成之無鹼玻璃。 SiO2 :55-80質量% Al2 O3 :8-20質量% B2 O3 :0-18質量% RO  0~17莫耳%(RO為MgO、CaO、SrO及BaO之總量) R’2 O  0~2莫耳%(R’2 O為Li2 O、Na2 O及K2 O之總量)。 根據減小熱收縮率之觀點,較佳為SiO2 為60~75質量%,進而為63~72質量%。 RO之中,較佳為MgO為0~10質量%,CaO為0~10質量%,SrO為0~10質量%,BaO為0~10質量%。 又,亦可為至少包含SiO2 、Al2 O3 、B2 O3 、及RO且莫耳比((2×SiO2 )+Al2 O3 )/((2×B2 O3 )+RO)為4.5以上之玻璃。又,較佳為包含MgO、CaO、SrO、及BaO之至少任一個,且莫耳比(BaO+SrO)/RO為0.1以上。 又,較佳為質量%表示之B2 O3 之含有率之2倍與質量%表示之RO之含有率之合計為30質量%以下,較佳為10~30質量%。 進而,熔融玻璃中價數變動之金屬之氧化物(氧化錫,氧化鐵)較佳為合計含有0.05~1.5質量%。 較佳為實質上不含有AS2 O3 、Sb2 O3 、PbO,但亦可任意地含有該等。 又,玻璃中價數變動之金屬之氧化物(氧化錫、氧化鐵)合計含有0.05~1.5質量%,且實質上不含有As2 O3 、Sb2 O3 及PbO之情況為任意而非必須。 本實施形態中製造之玻璃基板適合包含平板顯示器用玻璃基板之顯示器用玻璃基板。本實施形態中製造之玻璃基板適合使用有IGZO(銦、鎵、鋅、氧)等之氧化物半導體之氧化物半導體顯示器用玻璃基板及使用有LTPS(低溫多晶矽)半導體之LTPS顯示器用玻璃基板。又,本實施形態中製造之玻璃基板適合要求鹼金屬氧化物之含量極少之液晶顯示器用玻璃基板。又,亦適合有機EL顯示器用玻璃基板。換言之,本實施形態之玻璃基板之製造方法適合製造顯示器用玻璃基板,尤其適合製造液晶顯示器用玻璃基板。其他,亦可用作行動終端機器等之顯示器或殼體用之覆蓋玻璃、觸控面板、太陽電池之玻璃基板或覆蓋玻璃。本實施形態中製造之玻璃基板尤其適合使用多晶矽TFT之液晶顯示器用玻璃基板。 又,本實施形態中製造之玻璃基板亦可適用於覆蓋玻璃、磁碟用玻璃、太陽電池用玻璃基板等。 以上,對本實施形態之玻璃基板之製造方法及玻璃基板之製造裝置詳細地進行了說明,但本發明並非限定於上述實施形態,毋庸置疑,於不脫離本發明主旨之範圍內,可進行各種改良或變更。(實施例)利用使用高氧化鋯系耐火材料之溶解槽,將以具有下述組成之方式調配而成之玻璃原料電解溶解,形成熔融玻璃。繼而,利用鉑合金製之澄清管將所形成之熔融玻璃澄清之後,利用攪拌槽進行攪拌。繼而,將熔融玻璃供給至成形裝置200(成形體1),利用溢流下拉法成形平板玻璃。將平板玻璃之端部利用冷卻輥8以該端部之黏度成為1012.5 dPa・s之方式冷卻而成形之平板玻璃進行緩冷之後切斷,獲得厚度為0.4 mm且尺寸為2200 mm×2500 mm之平板顯示器用玻璃基板。再者,該玻璃組合物之液相黏度為50000 dPa・s,且應變點為715℃。SiO2 :61.5質量%,Al2 O3 :20質量%,B2 O3 :8.4質量%,CaO:10質量%,SnO2 :0.1質量%。使自玻璃供給管106供給至成形體1之供給槽2中之熔融玻璃之最大溫度差、熔融玻璃之黏度(基於平均溫度之黏度)進行變化,測定平板玻璃(玻璃基板)之板厚偏差。其結果示於表1中。[表1] 如表1所示,於熔融玻璃之最大溫度差為30℃以下且熔融玻璃之黏度(基於平均溫度之黏度)為22000 dPa・s以上38000 dPa・s以下之實施例1~6中,板厚偏差達到10 μm以下,從而可抑制板厚偏差。另一方面,於熔融玻璃之最大溫度差超過30℃之情形時、熔融玻璃之黏度(基於平均溫度之黏度)未達22000 dPa・s之情形時、及熔融玻璃之黏度超過38000 dPa・s之情形時之比較例1~7中,板厚偏差變得大於10 μm。藉此,可確認為使平板玻璃之板厚偏差成為10 μm以下,將供給至成形體1之供給槽2中之熔融玻璃之最大溫度差設為30℃以下,且將熔融玻璃之黏度(基於平均溫度之黏度)設為22000 dPa・s以上38000 dPa・s以下即可。Hereinafter, a method of producing the glass substrate of the present embodiment will be described. (Overall Outline of Manufacturing Method of Glass Substrate) Fig. 1 is a view showing an example of a procedure of a method for producing a glass substrate of the present embodiment. The method for producing a glass substrate mainly includes a dissolution step (ST1), a clarification step (ST2), a homogenization step (ST3), a supply step (ST4), a molding step (ST5), a slow cooling step (ST6), and a cutting step. (ST7). Others may have a grinding step, a grinding step, a washing step, an inspection step, a packing step, and the like. The glass substrate obtained by the production is stacked in the packing step as needed, and then transferred to the orderer. The dissolving step (ST1) is performed by heating a glass raw material to obtain a molten glass. The clarification step (ST2) produces oxygen and CO contained in the molten glass by heating the molten glass. 2 Or SO 2 Bubble. The bubble absorbs oxygen generated by a reduction reaction of a clarifying agent (tin oxide or the like) contained in the molten glass, and is floated to the liquid surface of the molten glass to be released. Thereafter, in the clarification step, since the temperature of the molten glass is lowered, the reducing substance obtained by the reduction reaction of the clarifying agent is subjected to an oxidation reaction. Thereby, the gas component such as oxygen in the bubble remaining in the molten glass is again absorbed into the molten glass, and the bubble is broken. The oxidation reaction and the reduction reaction carried out by the clarifying agent are carried out by controlling the temperature of the molten glass. Further, the clarification step may be a vacuum defoaming method in which the bubbles present in the molten glass are grown in a reduced pressure environment and then defoamed. The vacuum defoaming method is effective in not using a clarifying agent. However, the vacuum defoaming method causes the device to be complicated and enlarged. Therefore, it is preferred to use a clarifying method using a clarifying agent to raise the temperature of the molten glass. The homogenization step (ST3) performs homogenization of the glass component by stirring the molten glass using a stirrer. Thereby, the composition unevenness of the glass which is a cause such as a stripe can be reduced. The homogenization step is carried out in a stirred tank as described below. The supplying step (ST4) supplies the agitated molten glass to the forming apparatus. The forming step (ST5) and the slow cooling step (ST6) are carried out in a forming apparatus. The forming step (ST5) forms the molten glass into a flat glass to form a flat glass flow. In the forming process, an overflow down-draw method is employed. The slow cooling step (ST6) is a method in which the flat glass which is formed after the formation is formed to have a desired thickness and does not generate internal strain, and is cooled without causing warpage. In the cutting step (ST7), a plate-shaped glass substrate is obtained by cutting the slow-cooled sheet glass to a specific length. The obtained glass substrate was cut and cut into a specific size to prepare a glass substrate of a target size. Fig. 2 is a schematic view showing a manufacturing apparatus of a glass substrate in which the dissolving step (ST1) to the cutting step (ST8) in the present embodiment are performed. As shown in FIG. 2, the manufacturing apparatus of a glass substrate mainly has the dissolution apparatus 100, the shaping apparatus 200, and the cutting apparatus 300. The dissolution apparatus 100 has a dissolution tank 101, a clarification pipe 102, a stirring tank 103, transfer pipes 104 and 105, and a glass supply pipe 106. A heating mechanism such as a burner (not shown) is provided in the dissolution tank 101 shown in Fig. 2 . A glass raw material to which a clarifying agent has been added is introduced into the dissolution tank, and a dissolution step (ST1) is performed. The molten glass that has been melted in the dissolution tank 101 is supplied to the clarification pipe 102 via the transfer pipe 104. In the clarification pipe 102, the temperature of the molten glass MG is adjusted, and the clarification step (ST2) of the molten glass is performed by the oxidation-reduction reaction of the clarifying agent. Specifically, by heating the molten glass in the clarification pipe 102, the oxygen and CO contained in the molten glass are contained. 2 Or SO 2 The bubble absorbs oxygen generated by the reduction reaction of the clarifying agent to grow, floats to the liquid surface of the molten glass, and is released into the gas phase space. Thereafter, by reducing the temperature of the molten glass, the reducing substance obtained by the reduction reaction of the clarifying agent is subjected to an oxidation reaction. Thereby, the gas component such as oxygen in the bubble remaining in the molten glass is again absorbed into the molten glass, and the bubble is broken. The clarified molten glass is supplied to the stirring tank 103 via the transfer pipe 105. In the stirring tank 103, the molten glass is stirred by the stirring bar 103a, and the homogenization process (ST3) is performed. The molten glass which is homogenized in the stirring tank 103 is supplied to the molding apparatus 200 via the glass supply pipe 106 (supply step ST4). In the molding apparatus 200, the sheet glass SG is formed from the molten glass by the overflow down-draw method (forming step ST5), and the slow cooling is performed (slow cooling step ST6). In the cutting device 300, a plate-shaped glass substrate obtained by cutting out the sheet glass SG is formed (cutting step ST7). The supply step S4 controls the temperature of the molten glass flowing in the glass supply tube 106. Specifically, the glass supply pipe 106 is electrically heated to heat the molten glass flowing through the glass supply pipe 106, and the glass supply pipe 106 is surrounded by the refractory material, thereby suppressing the flow in the glass supply pipe 106. The heat dissipation of the molten glass. In the supply step S4, the temperature of the molten glass is controlled such that the temperature of the molten glass flowing through the glass supply pipe 106 gradually decreases from the upstream side toward the downstream side. The glass supply pipe 106 is divided into a plurality of zones, and the temperature of the molten glass is controlled by zones. The electric heating device for heating the glass supply pipe 106 controls the current and voltage flowing into the respective regions of the glass supply pipe 106 so that the temperature of the molten glass changes in accordance with the measurement data of the measuring device. The temperature of the molten glass supplied to the molding apparatus 200 can be appropriately changed by controlling the current and voltage in the glass supply pipe 106. Here, at the end portion on the downstream side of the glass supply pipe 106, the tube temperature and the center temperature of the molten glass are preferably from 1235 ° C to 1265 ° C, more preferably from 1240 ° C to 1260 ° C. (Configuration of the molded body) Next, the configuration of the molded body 1 included in the molding apparatus 200 will be described with reference to Figs. 3 and 4 . Fig. 3 shows an example of a molded article 1 which can be used in the manufacturing method of the present embodiment, and Fig. 4 shows an example of a forming step in the manufacturing method of the present embodiment using the molded article 1 shown in Fig. 3. The molded body 1 includes an upper surface 3 in which a supply tank 2 for supplying molten glass is formed, and a pair of wall surfaces 5 (only one wall surface is illustrated in FIGS. 3 and 4) which are guided from both sides of the supply tank 2 After the overflow, the molten glass flowing downward from between the end portions 3a, 3b of the upper surface 3 in the direction in which the supply groove 2 extends is merged into the flat glass SG at the lower end 4 of the molded body 1, and a pair of guides 6a And 6b are formed at positions of both end portions 5a and 5b in the width direction of the wall surface 5. The guides 6a and 6b are formed to face each other so as to protrude from the wall surface 5 at the positions of the end portions 5a and 5b. The molten glass overflowing from the supply tank 2 flows downward in each of the pair of wall faces 5. The wall surface 5 has a vertical wall surface in which the molten glass overflowing from the supply tank 2 flows downward in the vertical direction, and an inclined wall surface which is connected to the lower end 4 of the molten glass guide forming body 1 which flows downward from the vertical wall and is connected to the vertical wall surface. One of the convection systems of the molten glass flowing downward on the wall surface 5 merges at the lower end 4 of the formed body 1 so as to meet each other. At this time, the width of the molten glass flowing downward along the wall surface 5 is restricted by the guides 6a and 6b, thereby continuously forming, for example, the sheet glass SG having a high thickness uniformity in the width direction. The lower end 4 of the molded body 1 is formed as a linear ridge line in which a pair of wall surfaces 5 are connected to each other (inclined wall surfaces). The reference numeral 2a shown in Figs. 3 and 4 is the bottom surface 2a of the supply tank 2, and the reference numeral 7 shown in Fig. 3 is supplied to the liquid surface 7 of the molten glass of the supply tank 2. Here, the supply groove 2 of the molded body 1 has a shape of a bottom surface 2a which is a shape in which the molten glass supplied to the supply tank 2 overflows from the supply tank 2 in an extending direction of the supply tank 2 (melting glass) The flow direction) and the supply groove 2 orthogonal to the extending direction are uniform in the width direction. The flow rate of the molten glass flowing in the supply tank 2 is based on the viscosity based on the molten glass, the density of the molten glass, the depth from the liquid surface of the molten glass flowing in the supply tank 2 to the bottom surface 2a, and the width of the bottom surface 2a. Calculated. By the equation, the linear density of the flow rate of the molten glass is fixed in the flow direction from the groove start point side to the groove end point side of the glass supply pipe 106, that is, the overflow amount is uniform. The shape of the bottom surface 2a of the supply tank 2 is taken out. Further, the supply groove 2 at the position of the both end portions 3a, 3b of the molded body 1 has overflow from the molten glass to both sides of the supply groove 2 and is the same as the other portions from the positions of the both end portions 3a, 3b of the upper surface 3 The height of the ground surface 2a to the upper surface 3 is uniformly overflowed. When the molten glass overflows from both end portions 3a, 3b of the upper surface 3, the molten glass has a height from the upper surface 3 to the liquid surface of the molten glass. The intersection of the groove curve and the upper surface 3 including the shape of the bottom surface 2a obtained by subtracting the height from the bottom surface 2a to the liquid surface of the molten glass at the time of overflow from the upper surface 3 to the liquid surface of the molten glass becomes the supply tank 2 The end of the trough. Thereby, the distance from the groove start point to the groove end point of the supply groove 2 to which the glass supply pipe 106 is connected is determined, and the shape of the molded body 1 is determined. The cooling roll 8 is a unit which heat-treats both ends of the flat glass SG in the width direction. The cooling roll 8 is disposed on the downstream side of the lower end 4 of the molded body 1. Further, the cooling rolls 8 are disposed on both sides in the thickness direction of the sheet glass SG, and both sides in the width direction of the sheet glass SG. That is, the cooling roll 8 heat-treats the sheet glass SG which leaves the molded object 1 just below the molded object 1. The cooling rolls 8 disposed on both sides in the thickness direction of the sheet glass SG are operated in a paired shape. Therefore, both end portions in the width direction of the sheet glass SG are sandwiched by the pair of cooling rolls 8. The cooling roller 8 is air-cooled by an air cooling pipe leading to the inside. The cooling roller 8 is in contact with the end portion SGa of the sheet glass SG, and the end portion SGa of the sheet glass SG is quenched by heat conduction (end cooling step). The cooling roller 8 has a viscosity of 10 at the end portion SGa of the flat glass SG. 9.0 In the manner of dPa·s or more, the end portion SGa of the sheet glass SG is quenched. Further, the cooling roller 8 preferably has a viscosity of 10 at the end portion SGa of the flat glass SG. 9.0 ~10 14.5 In the range of dPa·s, the end portion SGa of the sheet glass SG is quenched. In the vicinity of each of the guides 6a and 6b, a heater is disposed so as to extend downward from the upper surface 3 side to the lower end 4 side of the molded body 1, and the molten glass which will flow downward toward the pair of wall faces 5 by the heater The portion in the vicinity of the guides 6a and 6b in the middle and the molten glass flowing downward in the wall surface 5 are heated. This heating is based on the viscosity of the portion near the guide members 6a, 6b in the molten glass flowing downward from the wall surface 5 from the upper surface 3 to the lower end 4 of the molded body 1 (the portion of the molten glass is from the upper surface of the molded body 1) 3, the downward flow reaches the lower end 4), and the liquid phase viscosity (hereinafter, also referred to simply as "liquidus viscosity") of the glass composition constituting the molten glass is not carried out along the guides 6a and 6b. In the formation of the sheet glass SG (and the production of the glass substrate obtained by cooling the sheet glass SG) by the overflow down-draw method using the molded article 1 having the guide member, it is easy to form the flat glass in the vicinity of the guide member. The end of the SG is devitrified. In this case, it is considered that the molten steel is formed into a viscosity suitable for molding at the lower end of the molded body 1 by the forming furnace for accommodating the molded body 1, and is usually set not only by the formation of the flat glass SG. For the purpose and also for the purpose of cooling the molten glass, that is, lower than the temperature of the molten glass, the heat of the molten glass is taken from the guides 6a, 6b, resulting in the temperature of the molten glass near the guides 6a, 6b. It is easy to be lower than the temperature of other portions in the molten glass; and, due to such a temperature drop and physical resistance caused by contact with the guide members 6a, 6b, the downward flow velocity of the molten glass in the vicinity of the guide members 6a, 6b is low. The other portion of the molten glass requires a long time or the like from the contact with the guides 6a, 6b until it leaves the molded body 1. According to Japanese Laid-Open Patent Publication No. 2010-215428, there is a possibility that the devitrification generated at the lower end of the guide can be suppressed. However, in the technique of this document, it is difficult to suppress the devitrification which occurs in the region upstream of the lower end of the guide member, especially in the initial stage of the contact between the molten glass and the guide member, and thus cannot be heated by the lower end of the guide member. One generation of devitrification is eliminated. Further, a glass composition having a liquidus temperature and a low liquid phase viscosity, such as an alkali-free glass and a trace amount of alkali glass, which are suitable for use in a glass substrate for a flat panel display, for example, is used in the production method of the present embodiment. Such a devitrification is particularly likely to occur in the case of a flat glass in which a glass composition having a liquidus viscosity of 80,000 dPa·s or more and 100,000 dPa·s or less and a liquidus temperature of 1200 ° C to 1,220 ° C is formed. In the manufacturing method of the present embodiment, the viscosity of the portion near the guide members 6a, 6b in the molten glass flowing downward on the wall surface 5 of the molded body 1 is maintained from the upper surface 3 to the lower end 4 of the molded body 1 The manner in which the viscosity of the liquid phase is reached (the temperature of the portion becomes higher than the liquidus temperature from the upper surface 3 to the lower end 4 of the molded body 1), and the portion in the molten glass is heated along the guides 6a, 6b. Thereby, a high effect of suppressing devitrification in a portion (the end portion of the molten glass) in the vicinity of the guide for the molten glass is obtained, and the glass composition constituting the molten glass has a density of 80,000 dPa·s or more and 100,000 dPa·s or less. In the case of a small liquid phase viscosity and a liquidus temperature in the range of 1200 ° C to 1220 ° C, the occurrence of devitrification in the end portion can also be suppressed. In the present specification, the liquid phase temperature refers to the equilibrium temperature between the melt and the initial phase of the crystallization, and if the temperature exceeds the temperature, there is no crystallization temperature, and the liquid phase viscosity means that the glass becomes the viscosity of the liquid phase temperature. . Fig. 5 is a view showing a cross section of the glass supply pipe 106 connected to the supply tank 2 of the molded body 1. In the glass supply pipe 106, if the temperature of the molten glass flowing in the central region 106a of the glass supply pipe 106 is compared with the temperature of the molten glass flowing in the peripheral region 106b, the temperature of the molten glass flowing in the central region 106a rises. high. When the molten glass is supplied to the supply tank 2 of the molded body 1 in a state where the temperature difference (viscosity difference) between the central region 106a and the peripheral region 106b is present, the molten glass is heated even in the space in which the molded body 1 is provided. The temperature difference of the molten glass is not improved from the glass supply tube 106 to the upper surface 3 of the molded body 1, but overflows from the upper surface 3 of the molded body 1 toward the lower end 4 in a state where the temperature difference of the residual molten glass is maintained. When there is a temperature difference in the molten glass at the time when the upper surface 3 of the molded body 1 overflows, the flow of the molten glass locally changes (stagnation), so that the molten glass does not uniformly overflow, and the wall surface 5 of the molded body 1 The thickness (amount) of the molten glass flowing downward changes, and the thickness of the sheet glass SG formed at the lower end 4 locally differs. Thereby, in the sheet glass SG, a local thickness variation including streaks occurs. Since both end portions SGa of the flat glass are cooled by the cooling roll 8, and the flat glass SG is applied with tension toward the both end portions SGa, the variation in the thickness of the sheet glass SG is reduced. In order to suppress the variation in the thickness of the sheet glass SG produced by the above-described principle to 10 μm or less, the maximum temperature difference between the molten glass in the glass supply tube 106 when the supply tank 2 of the molded body 1 is supplied, and the molten glass are used. Viscosity becomes more important. In the manufacturing method of the present embodiment, the maximum temperature difference of the molten glass when the glass supply tube 106 is supplied to the molding apparatus 200 (the supply tank 2 of the molded body 1) (the central region 106a of the glass supply tube 106 and the peripheral region 106b) The temperature difference is preferably 30° C. or lower, more preferably 20° C. or lower, and still more preferably 10° C. or lower. Further, the maximum viscosity difference of the molten glass (the difference in viscosity between the central region 106a of the glass supply tube 106 and the peripheral region 106b) is preferably 19,000 dPa·s or less, more preferably 12,500 dPa·s or less, and more preferably The best setting is 6200 dPa·s or less. Since the molten glass supplied to the supply tank 2 is heated in the space in which the molded body 1 is provided, the temperature difference of the molten glass is further smaller than the supply tank 2 from the supply tank 2 to the upper surface 3 of the molded body 1. The temperature difference at the time of supply is, for example, 10 ° C or lower. When the molten glass overflows from the upper surface 3 in such a temperature difference state, the molten glass uniformly overflows, and the thickness (amount) of the molten glass flowing downward on the wall surface 5 is uniform. The molten glass formed by confluence at the lower end 4 is formed into a sheet glass SG. The plate thickness of the sheet glass SG in the lower end 4 is greater than 10 μm, but the end portions SGa of the flat glass are cooled by the cooling roller 8 by applying tension to the both end portions SGa of the flat glass, the flat glass SG The local plate thickness deviation generated in the middle is 10 μm or less. The amount of variation in the thickness of the sheet which can be reduced by cooling the both end portions SGa of the flat glass affects the viscosity of the molten glass. In the production method of the present embodiment, when the molten glass is supplied to the molding apparatus 200 (the supply tank 2 of the molded body 1) via the glass supply pipe 106, the viscosity of the molten glass is preferably 22,000 dPa·s or more and 38,000 dPa·s or less. More preferably, it is 25,000 dPa·s or more and 38,000 dPa·s or less, and more preferably 25,000 dPa·s or more and 35,000 dPa·s or less. When the viscosity of the molten glass supplied to the supply tank 2 of the molded body 1 is lowered, that is, if the temperature of the molten glass is raised, the creep phenomenon of the molded body 1 becomes remarkable, and the time accompanying the start of the self-forming is also generated. After passing through, the central part of the flat glass is drooping and other problems. On the other hand, when the viscosity of the molten glass supplied to the supply tank 2 of the molded body 1 is raised, that is, when the temperature of the molten glass is lowered, the thickness variation of the flat glass tends to occur, and devitrification is likely to occur. Therefore, it is necessary to supply the molten glass which can suppress the creep phenomenon of the molded object 1 to the molded object 1 while preventing the variation in thickness and the occurrence of devitrification. The viscosity of the molten glass when the molding apparatus 200 is supplied is preferably 22,000 dPa·s or more and 38,000 dPa·s or less. The viscosity is determined by the glass composition due to the average viscosity of the molten glass. Hereinafter, the viscosity is referred to as an average viscosity-based viscosity. When the liquid phase viscosity of the glass composition constituting the molten glass is 80,000 dPa·s or more and 100,000 dPa·s or less, the lower end of the molded body 1 in which the viscosity of the molten glass formed by the molded body 1 is the highest is prevented. The viscosity of the molten glass is controlled so that the viscosity of the molten glass becomes less than 80,000 dPa·s. In order to suppress the creep phenomenon of the molded body 1, the viscosity of the molten glass supplied to the supply tank 2 of the molded body 1 is increased, and at the same time as the lower end of the molded body 1, the viscosity of the molten glass is less than 80,000 dPa·s. The molten glass is supplied to the supply tank 2 of the formed body 1. In the manufacturing method of the present embodiment, the viscosity of the molten glass supplied to the supply tank 2 of the molded body 1 (viscosity based on the average temperature) is from 22,000 dPa·s to 25,000 dPa·s, and the upper limit is from 35000 dPa.・s to 38000 dPa·s. Since the viscosity of the molten glass supplied to the supply tank 2 becomes small, the time from the supply of the molten glass to the supply tank 2 to overflow from the upper surface 3 becomes short. Therefore, during this time, the amount of heat received by the molten glass is reduced. The molten glass is heated in the supply tank 2 so that the temperature difference becomes small. However, if the time from the supply to the overflow is short, the temperature difference cannot be eliminated, and the temperature difference may occur. As a result, a portion where the speed of the downward flow locally changes occurs, and this causes a variation in the thickness of the plate. The sheet glass SG formed by converging at the lower end 4 of the molded body 1 by the viscosity (the viscosity based on the average temperature) of the molten glass supplied to the supply tank 2 of the molded body 1 is 22,000 dPa·s to 38000 dPa·s. The low viscosity is easily affected by the cooling effect of the cooling roll 8, and is pulled to the end side in the width direction, so that the effect of suppressing the thickness deviation of the sheet glass SG becomes large. On the other hand, when the molten glass has a low viscosity, the time until the overflow becomes short. Therefore, if there is a temperature difference (viscosity difference) of the molten glass, the thickness difference (viscosity difference) causes a variation in the thickness. Therefore, the maximum temperature difference of the molten glass supplied to the supply tank 2 is 30 degrees C or less. By supplying the molten glass satisfying the two conditions to the supply tank 2, the sheet thickness variation of the sheet glass SG can be 10 μm or less. In order to set the maximum temperature difference of the molten glass supplied to the supply tank 2 to 30 ° C or less, the temperature management of the molten glass flowing through the glass supply pipe 106 is important, and in the longitudinal direction of the tube of the glass supply pipe 106, such as As shown in Fig. 6, the plurality of cells SC1 to SC9 and the plurality of pipe segments PP1 to PP3 are divided to adjust the temperature. Fig. 6 is a graph showing changes in temperature of the molten glass flowing in the glass supply pipe 106 in the longitudinal direction of the tube of the glass supply pipe 106. In Fig. 6, the solid line L1 indicates the change in the "tube temperature" which is the temperature of the molten glass which is in contact with the inner peripheral surface of the glass supply tube 106, that is, the temperature of the glass supply tube 106, and the broken line L2 indicates the glass supply tube. The change in the "central temperature" of the temperature of the molten glass at the center of the profile of 106. In Fig. 6, the chain line L3 represents the average glass temperature obtained by weighted averaging of the mass flow rate of the molten glass per unit sectional area. Using the average temperature, the viscosity based on the average temperature of the molten glass was determined. The temperature change of the molten glass shown in FIG. 6 is described, and the molten glass obtained by homogenization in the molten glass homogenization step ST3 flowing into the glass supply pipe 106 flows into the first pipe section PP1 (zones SC1 to SC5). The difference between the tube temperature of the molten glass and the center temperature is zero. The first pipe section PP1 is used to cool the molten glass to a level not lower than the devitrification temperature of the glass. In the first pipe section PP1, the pipe temperature and the center temperature gradually decrease, and the difference between the pipe temperature and the center temperature gradually increases due to heat dissipation from the glass supply pipe 106. At the boundary between the first pipe section PP1 and the second pipe section PP2, the difference between the pipe temperature and the center temperature is preferably 100 ° C or less. In Fig. 6, in the first tube section PP1, the average glass temperature is lowered from 1470 °C to 1260 °C. In the second pipe section PP2, the drop in the tube temperature is suppressed. The current flowing in the second pipe section PP2 is higher than the current flowing in the first pipe section PP1. Therefore, the amount of heat supplied to the second pipe section PP2 by the energization heating is larger than the amount of heat given to the first pipe section PP1 by the energization heating. Therefore, in the second pipe section PP2, heat dissipation from the glass supply pipe 106 is suppressed, and the temperature of the glass supply pipe 106 is maintained substantially constant. At this time, in the second pipe section PP2, the molten glass from the center of the cross section of the glass supply pipe 106 is transferred toward the molten glass which is in contact with the inner peripheral surface of the glass supply pipe 106, and the center temperature gradually decreases. As a result, in the second pipe section PP2, there is a tendency that the difference between the tube temperature and the center temperature gradually decreases. At the boundary between the second pipe section PP2 and the third pipe section PP3, the difference between the pipe temperature and the center temperature is preferably 50 ° C or less. In Fig. 6, in the second tube section PP2, the average glass temperature is lowered from 1260 ° C to 1250 ° C. Further, in the seventh region SC7 of the second pipe segment PP2, the inner diameter of the glass supply pipe 106 is reduced. Therefore, in the second pipe section PP2, the area of the outer peripheral surface of the glass supply pipe 106 is gradually reduced, so that the heat dissipation of the molten glass via the glass supply pipe 106 is suppressed. That is, in the second pipe section PP2, the difference between the tube temperature and the center temperature is gradually reduced due to the two main factors of the application of the high current and the reduction of the inner diameter. In the third pipe section PP3, the maximum temperature difference between the tube temperature of the molten glass and the center temperature is 30 ° C or less. The refractory material surrounding the third pipe section PP3 is superior to the refractory material 106 surrounding the first pipe section PP1 and the second pipe section PP2. Therefore, the third pipe section PP3 is further suppressed from being radiated by the molten glass of the glass supply pipe 106 as compared with the first pipe section PP1 and the second pipe section PP2. Further, the current flowing in the third pipe section PP3 is lower than the current flowing in the second pipe section PP2, and the amount of heat supplied to the third pipe section PP3 by the energization heating is smaller than the amount of heat given to the second pipe section PP2 by the energization heating. Therefore, the temperature rise of the molten glass flowing in the third pipe section PP3 is suppressed. As a result, in the third pipe section PP3, the difference between the tube temperature and the center temperature is further reduced by the heat transfer in the molten glass in a state where the average glass temperature is substantially constant. In Fig. 6, in the third pipe section PP3, the average glass temperature is maintained at 1,250 °C. Further, a preferred range of the temperature of the molten glass passing through the glass supply tube 106 is as follows. The tube temperature and the center temperature are preferably 1420 ° C to 1470 ° C at the end portion on the upstream side of the glass supply pipe 106. Preferably, the tube temperature is 1210 ° C to 1260 ° C and the center temperature is 1300 ° C to 1350 ° C at the junction of the first tube section PP1 and the second tube section PP2. Preferably, the tube temperature is 1210 ° C to 1260 ° C and the center temperature is 1250 ° C to 1300 ° C at the junction of the second tube section PP2 and the third tube section PP3. The tube temperature and the center temperature are preferably 1235 ° C to 1265 ° C at the end portion of the downstream side of the glass supply pipe 106. The temperature difference of the molten glass by the glass supply pipe 106 is adjusted so that the maximum temperature difference of the molten glass supplied to the supply tank 2 is 30 degrees C or less. Further, since the measurement of the center temperature of the molten glass is difficult to use the thermometer, in this case, information on the amount of heat per unit time and unit area from the glass supply tube 106, and the unit of the glass supply tube 106 can be used. The information on the heating amount of time and unit area, and the temperature and flow rate of the molten glass when flowing into the glass supply pipe 106 are obtained by computer simulation based on the measurement results of the tube temperature of the glass supply pipe 106. Further, the tube temperature is measured by a thermometer (not shown) attached to each position of the glass supply tube 106. The viscosity is measured by a viscometer (not shown) attached to a portion where the glass supply tube 106 is connected to the supply tank 2 of the molded body 1. The viscometer uses, for example, a thin tube viscometer or a rotary viscometer. In the thin tube viscometer, the molten glass to be measured is passed through a thin tube, and the viscosity of the molten glass is measured according to the time (flow rate) of the molten glass passing through the thin tube and the pressure difference between both ends of the thin tube. The rotary viscometer measures the viscosity of the molten glass by reading the resistance which the molten glass receives from the rotating body, that is, the viscous resistance, based on the torque of the rotating body or the like. In the manufacturing method of the present embodiment, it is preferable that the temperature of the portion near the guide members 6a, 6b in the molten glass flowing downward from the wall surface 5 of the molded body 1 becomes the upper surface 3 to the lower end 4 of the molded body 1. The portion is heated so as to be higher than the liquidus temperature by 10 ° C or higher, and it is more preferable to heat the portion so as to be higher than the liquidus temperature by 15 ° C or higher. In such cases, the occurrence of devitrification in the end portion of the formed flat glass is more reliably suppressed. The specific liquidus temperature will vary depending on the composition of the glass composition. In the manufacturing method of the present embodiment, in the forming step, the temperature of the portion near the guide members 6a, 6b in the molten glass flowing downward from the wall surface 5 of the molded body 1 becomes the upper surface 3 of the molded body 1 to The lower end 4 is higher than the liquidus temperature by 10 ° C to 150 ° C (to be higher than the liquidus temperature by 10 ° C or more, and the liquidus temperature is increased by 150 ° C or less), along the guide Heat this part. Thereby, deformation of the molded body 1 and shrinkage in the width direction of the sheet glass SG after molding can be suppressed. Further, it is preferable that the temperature of the portion near the guide members 6a, 6b in the molten glass flowing downward from the wall surface 5 of the molded body 1 becomes higher than the liquidus temperature from the upper surface 3 to the lower end 4 of the molded body 1 The portion is heated along the guide in a manner of °C to 100 °C. The combination of the quenching of the end portion of the molten glass leaving the molded body 1 (quenching of the end portion SGa of the sheet glass SG) causes the sheet thickness variation of the sheet glass SG to be 10 μm or less. Moreover, the occurrence of devitrification in the end portion SGa is further reliably suppressed. Even if the temperature of the portion near the guides 6a, 6b in the molten glass flowing downward from the wall surface 5 of the molded body 1 is sufficiently higher than the liquidus temperature from the upper surface 3 to the lower end 4 of the molded body 1, The temperature of the entire molten glass flowing downward in the molded body 1 is sufficiently higher than the liquidus temperature, and theoretically, devitrification can be suppressed. However, in the case of producing a glass having a higher liquidus temperature, in reality, such an approach cannot be applied in the overflow down-draw method. The reason for this is that there is a viscosity of the molten glass which is suitable for the flat glass forming by the overflow down-draw method (the molten glass in the lower end 4 of the formed body 1 is used to avoid the problem of the relaxation of the flat glass described below or the width shrinkage of the flat glass). The viscosity is preferably 40,000 dPa·s or more, more preferably 70,000 dPa·s or more). When the temperature of the portion in the vicinity of the guide member in the molten glass becomes sufficiently higher than the liquidus temperature, the temperature of the entire molten glass flowing downward in the molded body 1 is sufficiently higher than the liquidus temperature, or When the lower end 4 of the molded body 1 is excessively heated, there is a possibility that the viscosity of the molten glass in the lower end 4 of the molded body 1 becomes smaller than the above-mentioned appropriate range. In this case, the viscosity of the sheet glass after leaving the molded body 1 is not sufficiently increased, and the flat glass falls at a speed higher than the stretching speed of the conveying roller disposed on the downstream side of the molded body 1, resulting in a lower speed. The flat glass is relaxed on the roll or the width of the flat glass is shrunk. Further, as the temperature of the molded body is higher, the creep phenomenon which changes with time with the use of the molded body becomes more remarkable, and the central portion of the flat glass also has a problem of sagging accompanying the passage of time from the start of the forming. Considering the thickness required for the glass substrate and the temperature control of the flat glass performed in the slow cooling step after forming, there is a limit to the increase in the stretching speed of the conveying roller (if the temperature control of the flat glass implemented in the slow cooling step is considered) The conveying speed of the flat glass is preferably from 50 to 500 m/hr, preferably from 100 to 400 m/hr, and preferably from 120 to 300 m/hr. Further, when the temperature of the portion in the vicinity of the guide in the molten glass is sufficiently higher than the liquidus temperature, the width of the formed flat glass is shrunk, and the product width as the glass substrate cannot be secured. In addition, when the temperature of the entire molten glass flowing downward in the molded body 1 is sufficiently higher than the liquidus temperature, the creep phenomenon of the molded body 1 occurs, and if the creep phenomenon becomes remarkable, the manufacturing is performed. The uniformity of the thickness of the glass substrate is lowered. The height of the guide protruding from the wall surface from which the molten glass flows in the molded body 1 is preferably as low as the position below the forming device. Preferably, the lower end 4 of the molded body 1 is a linear ridge line in which the inclined wall faces on both sides are connected to each other, and the height of the pair of guide members in the inclined wall surface is 0 (zero) at the position of the ridge line. Thereby, the end portion (ear portion) of the flat glass can be further inhibited from being opened in a bifurcated manner, so that the glass substrate can be continuously produced more stably. The amount of cooling and the amount of rotation of the cooling roll 8 are controlled by a control device (not shown). The control device mainly includes a computer such as a CPU, a RAM, a ROM, and a hard disk. The control device controls the drive motor that drives the cooling roller 8, and acquires and adjusts the contact load between one of the end portions SGa of the width direction of the holding plate glass SG and the cooling roller 8 and the sheet glass SG. The control device individually controls the amount of cooling of each of the cooling rolls 8. Further, the control device aims to set the cross-sectional shape in the thickness direction of the sheet glass SG to be described below as the target shape, and the tension applied to the sheet glass SG by the cooling control of the cooling roll 8 is at least the transfer unit and the acquisition unit. The four programs that the determination unit and the control unit function are stored and executed. In the conveyance unit, the sheet glass SG formed by the molded body 1 is conveyed to the lower side at a specific conveyance speed in a slow cooling space by using a conveyance roller provided below the molded body 1. The conveyance unit controls the drive motor that drives the conveyance roller to adjust the rotation speed of the conveyance roller, thereby adjusting the conveyance speed of the sheet glass SG. The acquisition unit acquires shape data relating to the current shape of the molded body 1 by obtaining a temporal change in the shape of the molded body 1 by computer simulation. Specifically, the acquisition unit acquires the shape data based on the creep characteristic parameter. The creep characteristic parameter is a parameter for reproducing the relationship between the stress applied to the formed body 1, the temperature of the formed body 1, and the strain rate of the formed body 1 due to creep deformation. Here, the stress applied to the molded body 1 compresses the force of the molded body 1 in the longitudinal direction of the molded body 1 (the extending direction of the supply groove 2). Further, the strain rate of the molded body 1 is assumed to be fixed without changing with time. First, the acquisition unit measures the strain rate of the molded body 1 under the condition that the stress applied to the molded body 1 is fixed, and changes the temperature of the molded body 1 in dependence. Then, the acquisition unit measures the strain rate of the molded body 1 under the condition that the temperature of the molded body 1 is fixed, and changes the stress depending on the stress applied to the molded body 1. Then, the acquisition unit determines a creep characteristic parameter that can reproduce the measured value of the temperature dependence change and the stress dependence change of the strain velocity of the molded body 1. Then, the acquisition unit calculates the strain velocity of the molded body 1 at a specific temperature and stress by computer simulation using the determined creep characteristic parameter, and obtains a time change of the shape of the molded body 1 to obtain a molded body. 1 shape information. Fig. 7 is an example of shape data of the molded body 1 obtained by the acquisition unit. Fig. 7 shows the obtained molded body 1 as viewed in a direction perpendicular to the surface of the sheet glass SG obtained by molding the formed body 1. In Fig. 7, the creep deformation of the formed body 1 is intensified as compared with the actual case. In Fig. 7, the shape of the molded body 1 which is not used, that is, the shape of the molded body 1 before the creep deformation is indicated by a broken line, and the current shape of the molded body 1 after the creep deformation is indicated by a solid line. The acquisition unit acquires at least the displacement amount in the vertical direction of the upper surface 3 of the molded body 1 from the shape data based on the creep deformation of the molded body 1, that is, the amount of displacement of the upper surface. In Fig. 7, the upper surface displacement amount is the dimension in the vertical direction between the upper surface 3 before the creep deformation and the upper surface 3 after the creep deformation. In addition, in FIG. 7, the maximum upper surface displacement amount L which is the maximum value of the surface displacement amount in the longitudinal direction of the molded object 1 is shown. Moreover, the acquisition unit acquires the thickness data of the glass substrate measured by the glass substrate shape measuring device (not shown). The thickness data is, for example, a distribution in the width direction of the thickness of the glass substrate manufactured by the molding apparatus 200. The determination unit determines whether or not the displacement amount L acquired by the acquisition unit has reached the reference amount. Here, the reference amount means a sheet thickness deviation when a flat tension (initial tension) is applied to the sheet glass SG, and the sheet glass SG (glass substrate) is formed into a predetermined thickness (for example, 0.1 mm to 0.8 mm). Can meet the amount of ± 10 μm. When the tension applied to the sheet glass SG is not changed from the initial value, if the displacement amount L exceeds the reference amount, the sheet thickness deviation of the sheet glass SG exceeds ±10 μm. Therefore, the thickness of the sheet glass SG is controlled so that the sheet thickness of the sheet glass SG becomes ±10 μm or less by increasing the tension applied to the sheet glass SG. The reference amount can be arbitrarily changed depending on the initial tension, the predetermined plate thickness of the sheet glass SG, the thickness deviation, and the like, and is, for example, 3 mm to 30 mm. The control unit is configured to apply a tension when the molded body 1 is not displaced in the width direction of the sheet glass SG (formed in the longitudinal direction of the molded body 1) and the cross-sectional shape in the thickness direction of the sheet glass SG is the target shape. The reference tension (initial tension) is controlled by controlling the cooling amount of the cooling roller 8 to cool both end portions SGa in the width direction of the sheet glass SG, whereby the tension applied to the sheet glass SG becomes the reference tension. . In a state in which the molded body 1 is not displaced, the sheet glass SG is formed into a predetermined sheet thickness by applying a reference tension in the width direction of the sheet glass SG, and the sheet thickness variation satisfies ±10 μm. When the tension applied to the sheet glass SG is always the reference tension in the state where the molded body 1 is creep-deformed, the target shape cannot be formed, for example, the sheet thickness cannot be formed into a predetermined shape, and the sheet thickness variation cannot satisfy ±10 μm. . Therefore, the control unit applies not only the reference tension but also the tension corresponding to the displacement of the formed body 1 to the sheet glass SG. Here, the displacement of the molded body 1 is, for example, the upper surface displacement of the molded body 1 in the longitudinal direction. The control unit controls the cooling so that the thickness of the flat glass SG becomes a predetermined thickness based on the shape data of the molded body 1 obtained by the acquisition unit, and the variation in the thickness of the flat glass SG in the width direction is small. The amount of cooling of the roller 8 thereby controls the tension applied to the sheet glass SG. The shape data of the molded body 1 is, for example, a distribution of the surface displacement amount in the longitudinal direction of the molded body 1, that is, a shape distribution. The control unit controls the amount of cooling of the cooling roller 8 so that the amount of displacement of the upper surface 3 is larger as the shape is distributed, and the tension in the width direction of the sheet glass SG is increased. As the displacement amount of the upper surface 3 obtained from the shape distribution, for example, the maximum upper surface displacement amount L is used. After the sheet glass SG formed at the lower end 4 of the molded body 1 is separated from the lower end 4, the central region SGb starts to contract toward the center in the width direction due to its surface tension. Therefore, the cooling roller 8 cools the both end portions SGa of the sheet glass SG to increase the viscosity of the both end portions SGa, and suppresses the contraction of the sheet glass SG in the width direction so that the tension is applied from the central portion SGb toward the both end portions SGa. The thickness of the central portion SGb of the sheet glass SG is uniform. However, when the molded body 1 is subjected to creep deformation, the amount of molten glass in the vicinity of the central portion SGb of the sheet glass SG increases, and the thickness of the central portion SGb changes. That is, the cross-sectional shape of the sheet glass SG in the thickness direction is no longer the target shape. Fig. 8 is a view showing the sheet glass SG in which the thickness in the vicinity of the central portion SGb is increased by the creep deformation of the molded body 1. When the molded body 1 is subjected to creep deformation, the amount of molten glass overflowing from between the end portion 3a of the upper surface 3 and the end portion 3b is increased, so that the thickness of the vicinity of the central portion SGb of the sheet glass SG is increased. In Fig. 8, the thickness in the vicinity of the central region SGb is at most thicker than the predetermined thickness D1, so that the thickness of the central region SGb becomes non-uniform. Therefore, the control unit changes the amount of cooling of the cooling roller 8 in accordance with the shape data of the molded body 1, and suppresses the contraction of the sheet glass SG in the width direction so as to apply tension from the central portion SGb of the sheet glass SG toward the both end portions SGa. The thickness of the central region SGb of the sheet glass SG is made uniform. Fig. 9 is a view showing the relationship between the maximum upper surface displacement amount L of the molded body 1 and the tension T applied to the sheet glass SG. In Fig. 9, the maximum upper surface displacement amount L is referred to as the displacement amount L. When the determination unit determines that the maximum upper surface displacement amount L of the molded body 1 does not exceed L1, the thickness of the central region SGb of the sheet glass SG caused by the creep deformation of the molded body 1 can be ignored. The tension T applied to the sheet glass SG is changed from the initial value T1 (the range of the displacement amount L: 0 or more and less than L1). When the displacement amount L of the molded body 1 is less than L1, the control unit does not change the cooling amount of the cooling roll 8, and maintains the tension T at the initial value T1, whereby the plate thickness deviation of the formed flat glass SG satisfies ±10 μm. . When the determination unit determines that the displacement amount L of the molded body 1 exceeds L1, the control unit controls the tension T corresponding to the maximum upper surface displacement amount L to be applied to the sheet glass SG as shown in FIG. 9 . If the maximum upper surface displacement amount L reaches L1 or more, as shown in Fig. 8, the thickness of the central portion SGb of the sheet glass SG is increased, and the thickness is no longer uniform. Therefore, the control unit controls the tension T=T1+A×maximum upper surface displacement amount L (the range of the displacement amount L: L1 or more and less than Lm, A) corresponding to the displacement amount L in such a manner as to correspond to the displacement amount L. The coefficient is applied to the sheet glass SG from the central portion SGb of the sheet glass SG toward both end portions SGa. The larger the deformation of the control portion molded body 1, the more the cooling of the both end portions SGa is enhanced. Specifically, the amount of cooling of the cooling rolls 8 is increased to increase the viscosity of the both end portions SGa. When the viscosity of the both end portions SGa is increased, the tension T from the central portion SGb toward the both end portions SGa is increased, and the molten glass located in the central portion SGb of the sheet glass SG is stretched toward both end portions SGa, so that the central region SGb The thickness is close to the predetermined thickness of the forming, and the thickness is uniform. The control unit is configured such that the viscosity of both end portions SGa is from, for example, 10 9.0 dPa·s increased to 10 14.5 From dPa·s, the tension T is increased to control. Further, when the maximum upper surface displacement amount L is in the range of L1 or more and less than Lm, by controlling the tension T to T1 to Tm, the thickness of the central portion SGb is close to a predetermined thickness, so that the thickness is uniform. However, when the displacement amount L exceeds Lm and is displaced, if only the tension T is controlled, it is difficult to make the thickness of the central region SGb close to the predetermined thickness, and the thickness is uniform. Therefore, it is determined by the determination unit. The periodic replacement period of the formed body 1 is reached. Further, due to the creep deformation of the molded body 1, the variation in the thickness of the plate glass SG (the surface unevenness) also changes. The volume shrinkage amount of the sheet glass SG increases as the end portion SGa from the sheet glass SG faces the center region SGb. Therefore, the tensile stress acts in the central portion SGb of the sheet glass SG. Since the thickness in the vicinity of the central region SGb is increased, the tension from the both end portions SGa toward the central region SGb is increased, so that the surface unevenness of the sheet glass SG is increased. Fig. 10 (a) is an enlarged view of a cross section taken along line AA of Fig. 4, and Fig. 10 (b) is an enlarged view of a cross section taken along line BB of Fig. 4. Before the tension T is applied to the sheet glass SG by the cooling roller 8, the sheet glass SG is shrunk toward the central portion SGb. Therefore, the surface unevenness of the sheet glass SG becomes D2, and after the tension T is applied to the sheet glass SG by the cooling roller 8, The surface unevenness of the sheet glass SG becomes D3 which is smaller than D2. When the molded body 1 is subjected to creep deformation, the surface unevenness D2 and D3 of the sheet glass SG also become large. Therefore, by applying the tension T from the central portion SGb toward the both end portions SGa so as to correspond to the maximum upper surface displacement amount L, the sheet glass SG is stretched toward the both end portions SGa, so that the surface of the flat glass SG is uneven. The difference D3 becomes smaller. In order to make the thickness of the central portion SGb close to the predetermined thickness, the surface unevenness D3 of the sheet glass SG is made smaller by applying the tension T in a manner corresponding to the maximum upper surface displacement amount L, so that the central portion of the flat glass SG The thickness of the SGb is uniform. Moreover, the control unit can suppress the presence of the streaks which are likely to occur in the conveyance direction of the sheet glass SG by applying the tension T to the sheet glass SG. The stripe is one of strains due to variations in thickness (height) of the sheet glass SG in a specific width range, and is continuously generated in a grain-like manner in the conveyance direction of the sheet glass SG. Moreover, the main factors of the stripe also include the difference in viscosity of the glass. When the tension is applied in the width direction of the sheet glass SG by the control unit controlling the amount of cooling of the cooling rolls 8, the locally generated streaks of the surface unevenness of the sheet glass SG are stretched to the both end sides of the sheet glass SG. SGa, so that the surface unevenness of the formed surface becomes small and the partial thickness deviation of the plate satisfies ±10 μm. As described above, the tension T in the width direction of the sheet glass SG applied to the sheet glass SG can be changed by the displacement amount due to the creep deformation of the formed body 1 by the lower end 4 of the molded body 1, while The thickness of the central portion SGb is close to the predetermined thickness, and the thickness is uniform. When the central portion of the longitudinal direction of the molded body 1 is sagged downward and is bent by the creep deformation of the molded body 1, the amount of cooling of the cooling roller 8 can be increased to apply the flat glass SG. The tension T in the width direction of the sheet glass SG becomes large, and the sheet thickness deviation in the width direction of the sheet glass SG is lowered. As a result, the variation in the thickness of the glass substrate as the final product can be reduced. Further, in the production step of using a glass substrate having a high liquidus temperature and a glass having a high strain point, the creep deformation of the molded body 1 is particularly likely to be a problem because the temperature of the molded body 1 is likely to increase. In addition, in recent years, as the size of the glass substrate is increased, the dimension of the longitudinal direction of the molded article is continuously increased. Therefore, the deflection of the molded body 1 due to creep deformation tends to be more remarkable. In the present embodiment, by adjusting the amount of cooling of the cooling roll 8, the tension T applied to the sheet glass SG can be changed, and the sheet in the width direction of the sheet glass SG due to the creep deformation of the formed body 1 can be effectively reduced. Thick deviation. According to the production method of the present embodiment, even when the liquid phase temperature of the glass composition constituting the molten glass is high and the liquidus viscosity is small, for example, when the glass composition is an alkali-free glass or a trace amount of alkali glass, Also, the effect of suppressing the devitrification in the end portion of the formed flat glass can be obtained. That is, when the temperature of the liquid phase of the glass composition constituting the molten glass is high and the viscosity of the liquid phase is small, the advantage obtained by the production method of the present embodiment is large. In the production method of the present embodiment, the glass composition constituting the molten glass has a liquidus viscosity of 10,000 dPa·s or less. Such glass compositions have previously been susceptible to devitrification problems in the ends of the flat glass of the overflow down draw process. However, in the production method of the present embodiment, the effect of suppressing devitrification can be obtained. The liquid glass viscosity of the molten glass used in the production method of the present embodiment is 100000 dPa·s or less. In the glass composition having a liquidus viscosity of 100,000 dPa·s or less, the above problem of devitrification becomes more remarkable, but the production method of the present embodiment has an effect of suppressing devitrification. The liquidus viscosity is preferably 80,000 dPa·s or more from the viewpoint of forming the flat glass which can stably perform the overflow down-draw method. The liquidus temperature of the glass composition constituting the molten glass used in the production method of the present embodiment is preferably 1200 ° C or more and 1220 ° C or less. Such glass compositions have previously been susceptible to devitrification problems in the ends of the flat glass of the overflow down draw process. However, the manufacturing method of the present embodiment has an effect of suppressing devitrification. In the production method of the present embodiment, the molten glass may contain zirconia and/or tin oxide. In the molten glass containing zirconia, the liquidus temperature of the glass composition rises as compared with the case where zirconium oxide is not contained. Such a molten glass is prone to devitrification problems in the end portion in the formation of the flat glass of the overflow down-draw method. However, the manufacturing method of the present embodiment has an effect of suppressing devitrification. Zirconium oxide can be eluted in the molten glass by using a dissolution tank and a molding apparatus using a high zirconia refractory material, even when the component of the glass composition is originally contained in the molten glass. In particular, when such a dissolution tank is used to electrolytically dissolve the glass raw material, the concentration of zirconia in the molten glass tends to increase. That is, the production method of the present embodiment is more suitable for the case where the glass raw material is electrolytically dissolved by using a dissolution tank composed of a high zirconia refractory. Further, the dissolution tank composed of the high zirconia refractory material is less likely to be corroded by the glass than the dissolution tank composed of the alumina electroformed refractory material which has been widely used in the past, and has a long service life as a dissolution tank. Moreover, foaming of the molten glass can also be suppressed. Therefore, it is suitable to form the melting temperature (the viscosity of the glass composition reaches 10) 2.5 The glass composition having a higher temperature is, for example, an alkali-free glass and a molten glass containing a trace amount of alkali glass. Further, when the molten glass formed by the dissolution tank contains an alkali-free glass or a trace amount of alkali glass, the electrical resistivity of the glass composition tends to become high, so that current flows into the high-zirconia refractory material without flowing into the glass raw material. tendency. When a current flows into the refractory, the zirconia is eluted in the molten glass formed by the dissolution tank. In other words, the production method of the present embodiment is further suitable for a case where an alkali-free glass or a molten glass containing a small amount of alkali glass is formed by electrolytic dissolution using a dissolution tank composed of a high zirconia-based refractory. In the glass substrate for an FPD (Flat Panel Display) such as a liquid crystal display or an organic EL display, a glass substrate containing an alkali-free glass or a trace amount of alkali glass is preferable. This is because if the alkali component is eluted from the glass substrate in the panel manufacturing step, the characteristics of the electronic component such as a thin film transistor (TFT) deteriorate. In other words, the production method of the present embodiment is particularly suitable for the case where a glass substrate for a flat panel display is produced by electrolytically dissolving a glass raw material using a dissolution tank composed of a high zirconia refractory material and using the obtained molten glass by an overflow down-draw method. . In addition, the alkali-free glass means a glass composition which does not substantially contain an alkali metal oxide (it is less than 0.05 mass % in terms of content rate). The alkali-containing glass refers to a glass composition containing 0.05 to 2.0% by mass of an alkali metal oxide. In molten glass containing tin oxide, devitrification is likely to occur due to crystallization of tin oxide. Further, in the case of coexistence with zirconia, tin oxide has a function of crystallizing zirconia. Such a molten glass is particularly prone to devitrification problems in the end portion during the process of forming the flat glass by the overflow down-draw method. However, the manufacturing method of the present embodiment has an effect of suppressing devitrification. In the production method of the present embodiment, the glass composition constituting the molten glass may be an alkali-free glass or a trace amount of alkali glass. Compared with an alkali glass containing more than 2.0% by mass of an alkali metal oxide, such an alkali-free glass or a trace amount of alkali glass tends to have a high liquidus temperature and a low liquid phase viscosity, but the production method of the present embodiment is obtained. The effect of suppressing devitrification. This effect is particularly remarkable as described above in the case where a molten glass containing an alkali-free glass or a small amount of alkali glass is formed by electrolytic dissolution using a dissolution tank composed of a high zirconia-based refractory. Further, the alkali-free glass is suitable for a glass substrate for a flat panel display from the viewpoint of preventing deterioration of characteristics of an electronic component such as a TFT (Thin Film Transistor). Among them, the alkali glass containing a trace amount is suitable for a glass substrate for flat panel displays from the viewpoint of solubility and clarification. The solubility and clarity of the glass composition are improved by making a trace amount of alkali glass by intentionally containing a trace amount of an alkali metal oxide. The alkalinity of the glass increases due to the presence of the alkali metal oxide, so that the metal whose valence is changed becomes easy to oxidize and contributes to clarification. Further, even when molten glass is formed by electrolytic dissolution of a glass raw material in a dissolution tank composed of a high zirconia refractory, the electrical resistivity of the glass can be made smaller than that of the alkali-free glass, so that the zirconia direction can be suppressed. The molten glass is eluted to suppress an increase in devitrification of the molten glass. In the production method of the present embodiment, in the case of the glass composition constituting the molten glass, 10 is presented. 2.5 The temperature of the viscosity of the poise (melting temperature) may also be 1500 ° C to 1750 ° C. Since such a glass composition requires a high temperature at the time of melting, when a molten glass is formed by the dissolution tank which consists of a high zirconia-type refractories, zirconia is melted easily. Even in such a glass composition, the production method of the present embodiment has an effect of suppressing devitrification. Examples of the glass component contained in the glass substrate produced by the production method of the present embodiment include SiO. 2 Al 2 O 3 , B 2 O 3 , MgO, CaO, SrO, BaO, Li 2 O, Na 2 O, K 2 O, ZrO 2 TiO 2 , ZnO, and P 2 O 5 . SiO 2 It is a skeleton component of glass and is therefore an essential component. When the content is small, the strain point is lowered and the coefficient of thermal expansion tends to increase. Also, if SiO 2 When the content is too small, it is difficult to reduce the density of the glass substrate. On the other hand, if SiO 2 When the content is too large, the electrical resistivity of the molten glass MG increases, and the melting temperature remarkably increases, which tends to be difficult to dissolve. If SiO 2 If the content is too large, the devitrification temperature rises and the devitrification resistance tends to decrease. Further, if SiO 2 If the content is too much, the etching rate becomes slow. According to this point of view, SiO 2 The content is preferably in the range of, for example, 60 to 80 mol%. SiO 2 The content is more preferably 64 to 73 mol% or 65 to 75 mol%, still more preferably 66 to 72 mol%, still more preferably 67 to 71 mol%. Al 2 O 3 It is necessary to raise the strain point. If Al 2 O 3 If the content is too small, the strain point is lowered. Further, if Al 2 O 3 When the content is too small, there is a tendency that the Young's modulus and the etching rate by oxygen are also lowered. On the other hand, if Al 2 O 3 When the content is too large, the devitrification temperature of the glass increases, and the devitrification resistance decreases, so that the formability tends to be deteriorated. According to this view, Al 2 O 3 The content is in the range of 8 to 20 mol%. Al 2 O 3 The content is preferably from 10 to 17 mol%, more preferably from 10.5 to 17 mol%, still more preferably from 11 to 15 mol%, still more preferably from 12 to 15 mol%. B 2 O 3 It reduces the high temperature viscosity of the glass and improves the composition of the meltability. That is, since the viscosity in the vicinity of the melting temperature is lowered, the solubility is improved. Also, B 2 O 3 It is also a component that lowers the devitrification temperature. If B 2 O 3 When the content is small, there is a tendency for solubility and devitrification resistance to decrease. If B 2 O 3 If the content is too much, the strain point and Young's modulus decrease. Also, since the glass is formed, B 2 O 3 Volatilization causes easy devitrification. In particular, since the glass having a high strain point tends to have a high molding temperature, the above-described volatilization is promoted, and the occurrence of devitrification becomes a significant problem. Also, when the glass dissolves, B 2 O 3 When it is volatilized, the heterogeneity of the glass becomes remarkable, and it becomes easy to generate streaks. According to this point of view, B 2 O 3 The content is 0 to 15 mol%, preferably 0 to 8 mol%, more preferably 0 to 7 mol%, still more preferably 0.1 to 6 mol%, still more preferably 1 to 5 mol%, still more preferably 1.5 to 4.5 mol%. The scope. MgO is a component that enhances solubility. Further, among the MgO-based alkaline earth metals, a component which is difficult to increase in density is required. Therefore, when the content is relatively increased, it is easy to achieve a low density. The resistivity and the melting temperature of the molten glass MG can be lowered by containing MgO. Among them, when the content of MgO is too large, the devitrification temperature of the glass sharply rises, so that devitrification is likely to occur particularly in the molding step. From such a viewpoint, the MgO content is 0 to 15 mol%, preferably 1 to 15 mol%, more preferably 0 to 6 mol%, still more preferably 1 to 6 mol%. Alternatively, the MgO content is preferably from 0 to 15 mol%, more preferably from 0 to 6 mol%, still more preferably from 1 to 6 mol%. The CaO system is a component which is effective in not increasing the devitrification temperature of the glass and increasing the solubility of the glass. Further, among the CaO-based alkaline earth metal oxides, a component which is difficult to increase in density is required. Therefore, when the content is relatively increased, it is easy to achieve a low density. When the content is too small, the electrical resistivity of the molten glass MG tends to increase and the devitrification resistance tends to decrease. If the CaO content is too large, the coefficient of thermal expansion increases and the density tends to increase. From such a viewpoint, the CaO content is 0 to 20 mol%, preferably 1 to 15 mol%, more preferably 2 to 11 mol%, still more preferably 4 to 9 mol%. The SrO system is capable of lowering the composition of the devitrification temperature of the glass. Although SrO is not essential, if it contains SrO, the devitrification resistance and solubility are improved. However, if the SrO content is too large, the density is increased. From such a viewpoint, the SrO content is 0 to 15 mol%, preferably 0 to 8 mol%, more preferably 0 to 3 mol%, still more preferably 0 to 1 mol%, still more preferably 0 to 0.5 mol%, Further preferably, it is substantially not contained. BaO is an essential component capable of effectively lowering the devitrification temperature of the glass and the electrical resistivity of the molten glass MG. When BaO is contained, the devitrification resistance and solubility are improved. However, if the content of BaO is too large, the density is increased. Further, the BaO content is 0 to 15 mol% or 0.1 to 15 mol%, preferably 1 to 15 mol%, more preferably 1 to 10 mol%, more preferably from the viewpoint of environmental load and a tendency to increase the coefficient of thermal expansion. It is in the range of 1.5 to 6 mol%. Li 2 O and Na 2 The O system has a component which increases the thermal expansion coefficient of the glass and causes damage to the substrate during heat treatment. Also, Li 2 O and Na 2 O is also a component that lowers the strain point. On the other hand, since the resistivity of the molten glass MG can be lowered, Li can be contained. 2 O and Na 2 O inhibits the dissolution tank from being eroded. According to the above point of view, Li 2 The content of O is preferably from 0 to 0.5 mol%, more preferably substantially not contained. Na 2 The content of O is preferably from 0 to 0.5 mol%, more preferably from 0 to 0.2 mol%. Furthermore, Na 2 O system and Li 2 O is preferably Na compared to a component which makes the strain point more difficult to reduce. 2 O>Li 2 O. Furthermore, Li is protected from the viewpoint of preventing deterioration of TFT characteristics due to elution from the glass substrate. 2 O and Na 2 O is preferably substantially not contained. K 2 The O system enhances the alkalinity of the glass to promote the clarifying component. Also, K 2 O is a component which lowers the specific resistance of the molten glass MG. If containing K 2 O, since the electrical resistivity of the molten glass MG is lowered, it is possible to prevent current from flowing into the refractory material constituting the dissolution tank, thereby suppressing erosion of the dissolution tank. Further, when the refractory material constituting the dissolution tank contains zirconia, the dissolution tank can be prevented from being eroded, and zirconia is eluted from the dissolution tank to the molten glass MG, so that devitrification caused by zirconia can also be suppressed. Further, since the viscosity of the glass in the vicinity of the dissolution temperature can be lowered, the solubility and clarity are improved. On the other hand, if K 2 When the content of O is too large, there is a tendency that the coefficient of thermal expansion increases and the strain point decreases. According to this point of view, K 2 The O content is preferably from 0 to 0.8 mol%, more preferably from 0.01 to 0.5 mol%, still more preferably from 0.1 to 0.3 mol%. ZrO 2 And TiO 2 A component that raises the strain point of the glass. However, if ZrO 2 Amount and TiO 2 If the amount is too large, the devitrification temperature rises remarkably, so that the devitrification resistance tends to decrease. Especially ZrO 2 The problem of refractory melting due to the high melting point causes a part of the raw material to be deposited on the bottom of the dissolution tank. When these undissolved components are mixed into the glass body, the quality of the glass is deteriorated as an inclusion. Also, TiO 2 Since the glass is colored, the substrate for the display is less preferable. According to such a viewpoint, in the glass substrate of the present embodiment, ZrO 2 And TiO 2 The content is preferably from 0 to 5 mol%, more preferably from 0 to 2 mol%, even more preferably substantially not contained. ZnO is a component that enhances solubility. But not a necessary ingredient. When the ZnO content is too large, the devitrification temperature rises, the strain point decreases, and the density tends to increase. From such a viewpoint, the ZnO content is preferably from 0 to 5 mol%, more preferably from 0 to 2 mol%, and further preferably substantially not contained. P 2 O 5 It is a component that lowers the viscosity of the high temperature and improves the solubility. But not a necessary ingredient. If P 2 O 5 If the content is too much, the strain point is lowered. Also, when the glass dissolves, P 2 O 5 The volatilization causes the non-homogeneity of the glass to become remarkable, and streaks are easily generated. According to this point of view, P 2 O 5 The content is preferably 0 to 3 mol%, more preferably 0 to 1 mol%, still more preferably 0 to 0.5 mol%, still more preferably substantially no content. The glass substrate to which the present embodiment is applied contains, for example, an alkali-free glass having the following composition. SiO 2 :55-80% by mass Al 2 O 3 : 8-20% by mass B 2 O 3 : 0-18 mass% RO 0 to 17 mol % (RO is the total amount of MgO, CaO, SrO and BaO) R' 2 O 0~2 mol% (R' 2 O is Li 2 O, Na 2 O and K 2 The total amount of O). From the viewpoint of reducing the heat shrinkage rate, SiO is preferred. 2 It is 60 to 75% by mass, and further 63 to 72% by mass. In the RO, MgO is preferably 0 to 10% by mass, CaO is 0 to 10% by mass, SrO is 0 to 10% by mass, and BaO is 0 to 10% by mass. Also, it may also contain at least SiO 2 Al 2 O 3 , B 2 O 3 And RO and Moer than (2 × SiO 2 )+Al 2 O 3 )/((2×B 2 O 3 ) +RO) is a glass of 4.5 or more. Further, it is preferable to contain at least one of MgO, CaO, SrO, and BaO, and the molar ratio (BaO+SrO)/RO is 0.1 or more. Also, preferably expressed in mass% B 2 O 3 The total content of the RO and the content of RO represented by the mass % are 30% by mass or less, preferably 10 to 30% by mass. Further, it is preferable that the oxide of the metal (tin oxide, iron oxide) whose valence varies in the molten glass is 0.05 to 1.5% by mass in total. Preferably, substantially no AS is included 2 O 3 , Sb 2 O 3 , PbO, but may also contain such arbitrarily. Further, the metal oxide (tin oxide, iron oxide) having a valence in the glass is contained in an amount of 0.05 to 1.5% by mass in total, and substantially does not contain As. 2 O 3 , Sb 2 O 3 And the case of PbO is arbitrary and not necessary. The glass substrate produced in the present embodiment is suitable for a glass substrate for a display including a glass substrate for a flat panel display. In the glass substrate produced in the present embodiment, a glass substrate for an oxide semiconductor display having an oxide semiconductor such as IGZO (indium, gallium, zinc, or oxygen) and a glass substrate for an LTPS display using an LTPS (low temperature polysilicon) semiconductor are suitably used. Further, the glass substrate produced in the present embodiment is preferably a glass substrate for a liquid crystal display which requires a very small content of an alkali metal oxide. Moreover, it is also suitable for a glass substrate for an organic EL display. In other words, the method for producing a glass substrate of the present embodiment is suitable for producing a glass substrate for a display, and is particularly suitable for producing a glass substrate for a liquid crystal display. Others can also be used as a cover glass for a mobile terminal device or the like, a cover glass for a housing, a touch panel, a glass substrate for a solar cell, or a cover glass. The glass substrate produced in the present embodiment is particularly preferably a glass substrate for a liquid crystal display using a polycrystalline germanium TFT. Further, the glass substrate produced in the present embodiment can also be applied to a cover glass, a glass for a disk, a glass substrate for a solar cell, or the like. The glass substrate manufacturing method and the glass substrate manufacturing apparatus of the present embodiment have been described in detail above. However, the present invention is not limited to the above-described embodiments, and it is needless to say that various modifications can be made without departing from the scope of the invention. Or change. (Example) A glass frit prepared by a composition having the following composition was electrolytically dissolved by a dissolution tank using a high zirconia refractory to form a molten glass. Then, the formed molten glass was clarified by a clarification tube made of a platinum alloy, and then stirred by a stirring tank. Then, the molten glass is supplied to the molding apparatus 200 (molded body 1), and the flat glass is formed by the overflow down-draw method. The end of the flat glass is made up of 10 by the chill roll 8 and the viscosity of the end is 10 12.5 The flat glass formed by cooling in the form of dPa·s was subjected to slow cooling and then cut to obtain a glass substrate for a flat panel display having a thickness of 0.4 mm and a size of 2200 mm × 2500 mm. Further, the glass composition had a liquidus viscosity of 50,000 dPa·s and a strain point of 715 ° C. SiO 2 : 61.5 mass%, Al 2 O 3 : 20% by mass, B 2 O 3 : 8.4% by mass, CaO: 10% by mass, SnO 2 : 0.1% by mass. The maximum temperature difference of the molten glass supplied from the glass supply pipe 106 to the supply tank 2 of the molded body 1 and the viscosity of the molten glass (viscosity based on the average temperature) were changed, and the variation in thickness of the flat glass (glass substrate) was measured. The results are shown in Table 1. [Table 1] As shown in Table 1, in the examples 1 to 6 in which the maximum temperature difference of the molten glass was 30 ° C or less and the viscosity of the molten glass (viscosity based on the average temperature) was 22,000 dPa·s or more and 38,000 dPa·s or less, the thickness was The deviation is less than 10 μm, so that the thickness deviation can be suppressed. On the other hand, when the maximum temperature difference of the molten glass exceeds 30 ° C, the viscosity of the molten glass (the viscosity based on the average temperature) is less than 22,000 dPa·s, and the viscosity of the molten glass exceeds 38,000 dPa·s. In the case of Comparative Examples 1 to 7, the sheet thickness deviation became larger than 10 μm. In this way, it is confirmed that the variation in the thickness of the flat glass is 10 μm or less, and the maximum temperature difference of the molten glass supplied to the supply tank 2 of the molded body 1 is 30° C. or less, and the viscosity of the molten glass is based on The viscosity of the average temperature is set to 22,000 dPa·s or more and 38,000 dPa·s or less.

1‧‧‧成形體
2‧‧‧供給槽
2a‧‧‧底面
3‧‧‧上表面
3a、3b‧‧‧(上表面之)端部
4‧‧‧下端
5‧‧‧壁面
5a、5b‧‧‧端部
6a、6b‧‧‧導件
7‧‧‧液面
8‧‧‧冷卻輥
100‧‧‧溶解裝置
101‧‧‧溶解槽
102‧‧‧澄清管
103‧‧‧攪拌槽
103a‧‧‧攪拌棒
104、105‧‧‧傳輸管
106‧‧‧玻璃供給管
106a‧‧‧中心區域
106b‧‧‧周邊區域
200‧‧‧成形裝置
300‧‧‧切斷裝置
D1‧‧‧增厚量
D2、D3‧‧‧平板玻璃SG之表面凹凸差
L(L1~Lm)‧‧‧位移量
MG‧‧‧熔融玻璃
PP1~PP3‧‧‧複數個管區段
SC1~SC9‧‧‧複數個區
SG‧‧‧平板玻璃
SGa‧‧‧(平板玻璃之)端部
SGb‧‧‧(平板玻璃之)中央區域
T(T1~Tm)‧‧‧張力
1‧‧‧Formed body
2‧‧‧ supply slot
2a‧‧‧ bottom
3‧‧‧ upper surface
3a, 3b‧‧‧ (top surface) end
4‧‧‧Bottom
5‧‧‧ wall
5a, 5b‧‧‧ end
6a, 6b‧‧‧ Guides
7‧‧‧ liquid level
8‧‧‧Cooling roller
100‧‧‧ Dissolving device
101‧‧‧Dissolution tank
102‧‧‧clarification tube
103‧‧‧Stirring tank
103a‧‧‧ stir bar
104, 105‧‧‧Transport tube
106‧‧‧Glass supply tube
106a‧‧‧Central area
106b‧‧‧ surrounding area
200‧‧‧Forming device
300‧‧‧cutting device
D1‧‧‧ thickening
D2, D3‧‧‧ surface glass SG surface unevenness
L (L1 ~ Lm) ‧ ‧ displacement
MG‧‧‧ molten glass
PP1~PP3‧‧‧Multiple pipe sections
SC1~SC9‧‧‧Multiple districts
SG‧‧ ‧ flat glass
SGa‧‧‧ (flat glass) end
Central area of SGb‧‧‧ (flat glass)
T (T1 ~ Tm) ‧ ‧ tension

圖1係表示本實施形態之製造方法之流程之圖。 圖2係玻璃基板之製造裝置之概略圖。 圖3係表示可於本實施形態之製造方法中使用之成形體之一例之立體圖。 圖4係說明使用圖3所示之裝置之本發明之製造方法之一例之圖。 圖5係表示與成形體之供給槽連接之玻璃供給管之剖面之圖。 圖6係表示本實施形態中使用之玻璃供給管之長邊方向上之於玻璃供給管之中流動之熔融玻璃之溫度變化之圖表。 圖7係說明利用獲取部所獲取之成形體之形狀變化之例之圖。 圖8係表示利用已蠕變變形之成形體成形所得之玻璃帶之剖面之一例之圖。 圖9係表示成形體之位移量與對玻璃帶施加之張力T之關係之圖。 圖10(a)係將沿著圖4所示之A-A線之平板玻璃之剖面之一例放大所得之圖,(b)係將沿著圖4所示之B-B線之平板玻璃之剖面之一例放大所得之圖。Fig. 1 is a view showing the flow of the manufacturing method of the embodiment. 2 is a schematic view showing a manufacturing apparatus of a glass substrate. Fig. 3 is a perspective view showing an example of a molded body which can be used in the production method of the embodiment. Fig. 4 is a view showing an example of a manufacturing method of the present invention using the apparatus shown in Fig. 3. Fig. 5 is a view showing a cross section of a glass supply pipe connected to a supply groove of a molded body. Fig. 6 is a graph showing the temperature change of the molten glass flowing in the glass supply tube in the longitudinal direction of the glass supply tube used in the present embodiment. Fig. 7 is a view showing an example of a shape change of a molded body obtained by an acquisition unit. Fig. 8 is a view showing an example of a cross section of a glass ribbon obtained by molding a molded body which has been subjected to creep deformation. Fig. 9 is a view showing the relationship between the displacement amount of the molded body and the tension T applied to the glass ribbon. Fig. 10(a) is an enlarged view of an example of a section of a plate glass along the line AA shown in Fig. 4, and (b) is an enlarged view of a section of a plate glass along the line BB shown in Fig. 4. The resulting map.

1‧‧‧成形體 1‧‧‧Formed body

2‧‧‧供給槽 2‧‧‧ supply slot

2a‧‧‧底面 2a‧‧‧ bottom

3‧‧‧上表面 3‧‧‧ upper surface

4‧‧‧下端 4‧‧‧Bottom

5‧‧‧壁面 5‧‧‧ wall

6a、6b‧‧‧導件 6a, 6b‧‧‧ Guides

7‧‧‧液面 7‧‧‧ liquid level

8‧‧‧冷卻輥 8‧‧‧Cooling roller

106‧‧‧玻璃供給管 106‧‧‧Glass supply tube

SG‧‧‧平板玻璃 SG‧‧ ‧ flat glass

SGa‧‧‧(平板玻璃之)端部 SGa‧‧‧ (flat glass) end

Claims (7)

一種玻璃基板之製造方法,其特徵在於:其係將熔融玻璃自玻璃供給管供給至具有供給槽之成形體,使用上述成形體藉由溢流下拉法成形平板玻璃者,上述供給槽具有供給至上述供給槽之熔融玻璃自上述供給槽溢出之量於上述供給槽之延伸方向、及與上述延伸方向正交之寬度方向上形成均一之底面形狀,上述玻璃基板之製造方法具有:成形步驟,其係將自上述玻璃供給管供給至上述供給槽之熔融玻璃之最大溫度差為30℃以下且熔融玻璃之黏度為22000 dPa・s以上38000 dPa・s以下之熔融玻璃供給至上述供給槽,且於上述成形體之下端使上述熔融玻璃匯流,而成形平板玻璃;及 端部冷卻步驟,其係以抑制上述成形步驟中成形所得之上述平板玻璃中局部地產生之板厚偏差之方式,將平板玻璃之寬度方向之兩端部冷卻。A method for producing a glass substrate, which is characterized in that molten glass is supplied from a glass supply tube to a molded body having a supply groove, and the flat glass is formed by an overflow down-draw method using the molded body, and the supply tank is supplied to the molten glass. The molten glass overflowing from the supply tank is formed in a direction in which the supply groove extends and a uniform bottom surface shape in a width direction orthogonal to the extending direction, and the method for producing the glass substrate includes a molding step. The molten glass having a maximum temperature difference of 30° C. or less from the molten glass supplied from the glass supply pipe to the supply tank and having a viscosity of 22000 dPa·s or more and 38,000 dPa·s or less of the molten glass is supplied to the supply tank, and a flat glass is formed by converging the molten glass at a lower end of the molded body, and an end cooling step of suppressing a thickness variation locally generated in the flat glass obtained by molding in the forming step. Both ends in the width direction are cooled. 如請求項1之玻璃基板之製造方法,其中 上述端部冷卻步驟係將上述成形體於上述平板玻璃之寬度方向上未變形時施加之上述平板玻璃之剖面形狀成為目標形狀之張力設為基準張力,於上述成形體未變形時,以藉由將上述平板玻璃之寬度方向之兩端部冷卻而成為上述基準張力之方式進行控制,且於上述成形體產生變形時,對於上述平板玻璃施加根據上述成形體之變形而與上述基準張力相加之張力。The method of producing a glass substrate according to claim 1, wherein the end portion cooling step is a reference tension when a cross-sectional shape of the flat glass applied to the flat glass in the width direction of the flat glass is a target shape. When the molded body is not deformed, it is controlled such that the both ends of the flat glass in the width direction are cooled to be the reference tension, and when the molded body is deformed, the flat glass is applied according to the above. The deformation of the molded body and the tension added to the above reference tension. 如請求項2之玻璃基板之製造方法,其中上述成形體之變形係伴隨著上述成形體之使用而經時變化之蠕變變形,且對上述基準張力加上與上述蠕變變形造成之上述成形體之特定位置之位移量相應之張力。The method for producing a glass substrate according to claim 2, wherein the deformation of the molded body is a creep deformation which changes with time with the use of the molded body, and the forming of the reference tension is caused by the creep deformation. The amount of displacement of a particular position of the body corresponds to the tension. 如請求項2或3之玻璃基板之製造方法,其中上述變形愈大則愈增強上述兩端部之冷卻。The method for producing a glass substrate according to claim 2 or 3, wherein the larger the deformation, the more the cooling of the both end portions is enhanced. 如請求項1至4中任一項之玻璃基板之製造方法,其中 上述板厚偏差為10 μm以下。The method for producing a glass substrate according to any one of claims 1 to 4, wherein the thickness deviation is 10 μm or less. 如請求項1至5中任一項之玻璃基板之製造方法,其中 於上述成形步驟中,以於上述成形體向下流動之熔融玻璃之溫度相較上述熔融玻璃之液相溫度增高10℃~150℃之方式,加熱上述熔融玻璃。The method for producing a glass substrate according to any one of claims 1 to 5, wherein, in the forming step, the temperature of the molten glass flowing downward from the molded body is increased by 10 ° C from the liquidus temperature of the molten glass. The above molten glass was heated at 150 °C. 一種玻璃基板之製造裝置,其特徵在於:其係將熔融玻璃自玻璃供給管供給至具有供給槽之成形體,且使用上述成形體藉由溢流下拉法成形平板玻璃,上述成形體具有接收最大溫度差為30℃以下且黏度為22000 dPa・s以上38000 dPa・s以下之熔融玻璃供給之供給槽、及用以於上述成形體之下端使上述熔融玻璃匯流而成形平板玻璃之壁面,上述供給槽具有供給至上述供給槽之熔融玻璃自上述供給槽溢出之量於上述供給槽之延伸方向及與上述延伸方向正交之寬度方向上形成均一之底面形狀, 上述玻璃基板之製造裝置更具備以抑制藉由上述成形體成形所得之上述平板玻璃中局部地產生之板厚偏差之方式冷卻平板玻璃之寬度方向之兩端部之端部冷卻裝置。A glass substrate manufacturing apparatus characterized in that molten glass is supplied from a glass supply pipe to a molded body having a supply groove, and the flat glass is formed by an overflow down-draw method using the molded body, and the molded body has a maximum receiving amount. a supply groove for supplying molten glass having a temperature difference of 30 ° C or less and a viscosity of 22,000 dPa·s or more and 38,000 dPa·s or less, and a wall surface for forming the flat glass by converging the molten glass at the lower end of the molded body, the supply The groove has a uniform bottom surface shape in which the molten glass supplied to the supply tank overflows from the supply tank in a direction in which the supply groove extends and a width direction orthogonal to the extending direction, and the glass substrate manufacturing apparatus further includes An end portion cooling device that cools both end portions in the width direction of the flat glass so as to suppress variation in thickness locally generated in the flat glass obtained by molding the molded body is suppressed.
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