TW201141803A - Glass melting furnace and method for melting glass - Google Patents
Glass melting furnace and method for melting glass Download PDFInfo
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- TW201141803A TW201141803A TW100114500A TW100114500A TW201141803A TW 201141803 A TW201141803 A TW 201141803A TW 100114500 A TW100114500 A TW 100114500A TW 100114500 A TW100114500 A TW 100114500A TW 201141803 A TW201141803 A TW 201141803A
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- glass
- burner
- melting
- burners
- air
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- 238000002844 melting Methods 0.000 title claims abstract description 162
- 230000008018 melting Effects 0.000 title claims abstract description 162
- 239000011521 glass Substances 0.000 title claims abstract description 107
- 238000000034 method Methods 0.000 title claims description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 89
- 239000001301 oxygen Substances 0.000 claims abstract description 89
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 89
- 238000002485 combustion reaction Methods 0.000 claims abstract description 78
- 239000007789 gas Substances 0.000 claims description 48
- 239000000446 fuel Substances 0.000 claims description 36
- 239000002994 raw material Substances 0.000 claims description 27
- 238000004090 dissolution Methods 0.000 claims description 11
- 239000007921 spray Substances 0.000 claims description 3
- 239000000284 extract Substances 0.000 claims 1
- 239000006060 molten glass Substances 0.000 abstract description 73
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 60
- 230000001105 regulatory effect Effects 0.000 abstract description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 36
- 239000003345 natural gas Substances 0.000 description 19
- 238000010438 heat treatment Methods 0.000 description 18
- 238000005352 clarification Methods 0.000 description 13
- 238000004519 manufacturing process Methods 0.000 description 7
- 239000000295 fuel oil Substances 0.000 description 6
- 230000007547 defect Effects 0.000 description 5
- 238000007667 floating Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000004364 calculation method Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000007670 refining Methods 0.000 description 3
- 239000000567 combustion gas Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 238000013022 venting Methods 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000282342 Martes americana Species 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 210000000078 claw Anatomy 0.000 description 1
- 238000005202 decontamination Methods 0.000 description 1
- 230000003588 decontaminative effect Effects 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052743 krypton Inorganic materials 0.000 description 1
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000006166 lysate Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B5/00—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture
- C03B5/16—Special features of the melting process; Auxiliary means specially adapted for glass-melting furnaces
- C03B5/235—Heating the glass
- C03B5/2353—Heating the glass by combustion with pure oxygen or oxygen-enriched air, e.g. using oxy-fuel burners or oxygen lances
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B5/00—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture
- C03B5/04—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture in tank furnaces
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B5/00—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture
- C03B5/16—Special features of the melting process; Auxiliary means specially adapted for glass-melting furnaces
- C03B5/235—Heating the glass
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P40/00—Technologies relating to the processing of minerals
- Y02P40/50—Glass production, e.g. reusing waste heat during processing or shaping
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Glass Melting And Manufacturing (AREA)
Abstract
Description
201141803 六、發明說明: 【發明所屬之技術領域】 本發明係關於一種熔解玻璃原料之玻璃熔解爐及玻璃熔 解方法。 【先前技術】 製造玻璃製品之方法一般而言係藉由炫解玻璃原料而獲 得嫁融玻璃之熔解步驟;去除熔融玻璃之氣泡而澄清熔融 玻璃之澄清步驟;及將澄清後之熔融玻璃成形為特定之形 狀之成形步驟所構成。 該等步驟中,熔解步驟係將複數種原料對照玻璃製品之 組成而稱量並混合所得之玻璃原料投入熔解爐中,並加熱 至與玻璃之種類相應之溫度而使其溶解的步驟。 熔解爐係於熔解玻璃原料之熔解室之前壁具備原料投入 口,於熔解室之後壁具備取出口’於自原料投入口至取出 口之流路之側壁具備複數個燃燒器,並使複數個燃燒器向 熔解室内喷出火焰而將熔解室内之玻璃加熱熔解者。燃燒 器喷出使天然氣或重油等燃料與氣體混合並燃燒所產 火焰。 一般而言,作為混合於燃料中之氣體,使用空氣及氧氣 之任-者。於使用有空氣之空氣燃燒之情形時,佔空氣之 約78體積%之氛氣無助於燃燒而被排氣至爐外。於使用有 氧氣之氧燃燒之情形時,與空氣燃燒之情形相&,排氣量 較厂故熱效率較高,C〇2排出量或ΝΟχ排出量較少。 作為混合於燃料中之氣體,亦有可能使用由空氣與氧氣 155915.doc I » 201141803 混合而成之混合氣體(例如參照專利文獻1}。該情形時,混 合氣體中所佔氧氣之比例越高,則燃燒後之氣體中所含之 水分濃度越高,因此熔解室内之熔融玻璃令溶存之水分量 變多。溶融玻璃中溶存之水分於澄清步驟中成為氣泡Z 浮。因此’藉由使炫融玻璃中溶存之水分量最佳化而於澄 清步驟中可促進熔融玻璃内之氣泡之成長,促進氣泡之上 浮,從而可製造缺陷較少的玻璃製品。 然而,作為混合於燃料中之氣體,於使用將空氣與氧氣 混合而成之混合氣體之情形時,與空氣燃燒之情形相比, 亦存在有NOx排出量變多(例如,參照非專利文獻丨)。詳細 而言,於混合氣體中之氧濃度未滿93體積%且超過乃體積 %之情形時,與空氣燃燒之情形相比,Ν〇χ排出量變多。 先前技術文獻 專利文獻 專利文獻1 :日本國專利特開2000-128549號公報 非專利文獻 非專利文獻 1 : Research & Development,Kobe Steel Engineering Reports,Vol.51,編號 2(Sep.2001) ’ ρ·8 〜12,「關於富氧空 氣之省能源化與低ΝΟχ燃燒之研究」 【發明内容】 發明所欲解決之問題 對此’本發明為了抑制C〇2或ΝΟχ之排出量之增加並調 節熔解室内之熔融玻璃中溶存之水分量,而研究將空氣燃 燒器與氧燃燒器之兩者設置於熔解爐中。 155915.doc 201141803 然而’若將空氣燃燒器與氧燃燒器之兩者僅設置於熔解 爐中’則藉由設置於熔解室之側壁之排氣口之影響,有時 難以充分調節熔解室内之燃燒後之氣體中所含之水分濃 度。其結果有如下情形:充分調節熔解室内之熔融玻璃中 溶存之水分量變得困難。 本發明係雲於上述課題而完成者,其目的在於提供一種 可抑制C〇2或NOx之排出量之增加、且可充分調節熔融玻 璃中溶存之水分量的玻璃溶解爐。 解決問題之技術手段 為解決上述目的,本發明係一種玻璃熔解爐,其包含熔 解玻璃原料之熔解室、及設置於該熔解室之自前壁到達後 壁之流路之側壁的複數個燃燒器,上述複數個燃燒器向上 述熔解室内噴出火焰而將上述熔解室内之玻璃加熱並熔 解; 上述複數個燃燒器中係使用喷出使燃料與氧氣混合並燃 燒所產生之火焰之氧燃燒器、及喷出使燃料與空氣混合並 燃燒所產生之火焰之空氣燃燒器之兩者, 上述複數個燃燒器每1小時之總燃燒熱量之3〇%以上9〇% 以下係由上述氧燃燒器而產生, 將用以使上述熔解室内之燃燒後之氣體向外部排氣之排 氣口於上述熔解室之兩側壁之各自上相對向地僅配置有i 個,僅配置於上述溶解室之兩側壁之—方且僅配置有i 個,或者配置於上述熔解室之前壁或後壁, 若將上述排氣口與上述前壁之間的前後方向上之距離及 155915.doc 201141803201141803 VI. Description of the Invention: [Technical Field of the Invention] The present invention relates to a glass melting furnace for melting a glass raw material and a glass melting method. [Prior Art] A method of producing a glass article generally comprises a melting step of obtaining a marten glass by dissipating a glass raw material; a clarifying step of removing the bubbles of the molten glass to clarify the molten glass; and forming the clarified molten glass into The shaping step of a specific shape is formed. In the above steps, the melting step is a step of weighing and mixing the glass raw materials obtained by mixing the plurality of raw materials against the composition of the glass product into a melting furnace, and heating to a temperature corresponding to the type of the glass to dissolve. The melting furnace is provided with a raw material input port on the wall of the melting chamber of the molten glass raw material, and has a plurality of burners on the side wall of the flow path from the raw material input port to the take-out port after the melting chamber is provided, and the plurality of burners are combusted The device sprays a flame into the melting chamber to heat and melt the glass in the melting chamber. The burner is sprayed to mix a fuel such as natural gas or heavy oil with a gas and burn the flame. In general, as a gas mixed in a fuel, any of air and oxygen is used. In the case of burning with air, air containing about 78% by volume of air does not contribute to combustion and is exhausted to the outside of the furnace. When using oxygen-burning oxygen, it is more efficient than the case of air combustion. The exhaust gas volume is higher than that of the plant, and the C〇2 discharge amount or the krypton discharge amount is small. As a gas mixed in the fuel, it is also possible to use a mixed gas obtained by mixing air and oxygen 155915.doc I » 201141803 (for example, refer to Patent Document 1). In this case, the proportion of oxygen in the mixed gas is higher. The higher the concentration of water contained in the gas after combustion, the larger the amount of water dissolved in the molten glass in the melting chamber. The water dissolved in the molten glass becomes the bubble Z in the clarification step. The amount of water dissolved in the glass is optimized, and in the clarification step, the growth of the bubbles in the molten glass is promoted, and the floating of the bubbles is promoted, so that a glass product having less defects can be produced. However, as a gas mixed in the fuel, When a mixed gas obtained by mixing air and oxygen is used, the amount of NOx emission is also increased as compared with the case of air combustion (for example, refer to Non-Patent Document 丨). In detail, oxygen in a mixed gas When the concentration is less than 93% by volume and exceeds 5% by volume, the amount of ruthenium discharge is increased as compared with the case of air combustion. Patent Document Patent Document 1: Japanese Patent Laid-Open No. 2000-128549 Non-Patent Document Non-Patent Document 1: Research & Development, Kobe Steel Engineering Reports, Vol. 51, No. 2 (Sep. 2001) 'ρ·8 〜 12, "Research on Energy Saving and Low-Temperature Combustion of Oxygen-Enhanced Air" [Disclosure] The problem to be solved by the present invention is to reduce the amount of discharge of C〇2 or ΝΟχ and to adjust the melting chamber. The amount of water dissolved in the molten glass, and it is studied to set both the air burner and the oxygen burner in the melting furnace. 155915.doc 201141803 However, if both the air burner and the oxygen burner are set only in the melting furnace In the middle, it is difficult to sufficiently adjust the concentration of water contained in the gas after combustion in the melting chamber by the influence of the exhaust port provided on the side wall of the melting chamber. As a result, there is a case where the molten glass in the melting chamber is sufficiently adjusted. The amount of water dissolved in the medium becomes difficult. The present invention has been accomplished in the above-mentioned problems, and an object thereof is to provide an increase in the amount of discharge of C〇2 or NOx. A glass melting furnace capable of sufficiently adjusting the amount of water dissolved in the molten glass. Technical Solution to Problem In order to solve the above object, the present invention is a glass melting furnace comprising a melting chamber for melting a glass raw material, and a melting chamber disposed therein a plurality of burners from the front wall to the side wall of the flow path of the rear wall, wherein the plurality of burners spray a flame into the melting chamber to heat and melt the glass in the melting chamber; and the plurality of burners are used to eject An oxygen burner that mixes the fuel with oxygen and combusts the generated flame, and an air burner that ejects a flame that is mixed with the fuel and combusted, and the total combustion heat per hour of the plurality of burners 3% or more and 9% by weight or less are generated by the oxygen burner, and an exhaust port for exhausting the burned gas in the melting chamber to the outside is opposed to each other on both side walls of the melting chamber Only i are disposed in the ground, and are disposed only on the two side walls of the dissolution chamber, and are disposed only in i or disposed on the front wall or the rear of the melting chamber. , If the distance between the longitudinal direction of the exhaust port and the front wall and 155915.doc 201141803
上述排氣口與上述後壁之間的前後方向上之距離中之最大 距離設為L,則於自上述排氣口朝前方及/或後方離開〇 6L 以上之區域中’各設置有至少1個上述氧燃燒器及上述空 氣燃燒器, 設置於該區域之上述燃燒器每!小時之總燃燒熱量中的 5%以上95%以下係由上述空氣燃燒器而產生。 發明之效果 根據本發明,可提供一種可抑制1^〇?{排出量之增加、且 可充分調節熔融玻璃中溶存之水分量之玻璃熔解爐。該玻 璃熔解爐於對熔融玻璃進行充分加熱並使水分量降低之情 形時特別有效。 【實施方式】 以下,參照圖式對用以實施本發明之形態進行說明。再 者,於各圖中,對於相同構成標註相同符號並省略其說 明。 (第1實施形態) 圖1係本發明之實施形態之玻璃製品之製造方法之步驟 圖。圖2係第1實施形態之玻璃熔解爐之内部結構之側視 圖。圖3係第1實施形態之玻璃熔解爐之内部結構之俯視 圖。於圖3中,將各燃燒器之燃燒區域(各燃燒器之火焰之 外緣)以虛線包圍而表示。 如圖1所示,玻璃製品之製造方法包括:熔解玻璃原料 而獲得熔融玻璃之熔解步驟(sl〇〇);去除熔融玻璃之氣泡 而澄清熔融玻璃之澄清步驟(sl〇2):及將澄清後之熔融玻 1559l5.doc 201141803 璃成形為特定形狀之成形步驟(S104)。 該等步驟中,澄清步驟(S1G2)係將輯步驟中所得之溶 融玻璃供給至澄清槽,使熔融玻璃内之氣泡上浮並加r 除的步驟。作為促進氣泡上浮之方法,有例如對澄二: 進行減壓而脫泡之方法等。 成形步驟(S1G4)係將澄清後之㈣玻璃成形為特定板厚 之板狀的步驟。作為成形為板狀之方法,有例如周知之浮 式法、熔合法。 熔解步驟(S100)係將複數種原料對照玻璃製品之組成而 稱量並混合所得之玻璃原料投入熔解爐中,加熱至與玻璃 之種類相應之溫度而使其熔解的步驟。 如圖2、圖3所示,熔解爐丨係於熔解玻璃原料之熔解室 10之上游側之前壁Η具備原料投入口21,於熔解室1〇之下 游側之後壁12具備取出口22,於自原料投入口21到達取出 口 22之流路23之兩側壁13、14具備複數個燃燒器31〜5〇及1 對排氣口 24 ' 25。兩側壁13、14在前後方向上延伸。 該熔解爐1中,自原料投入口21投入之玻璃原料⑴係與 熔解至10内之熔融玻璃G2—併藉由來自複數個燃燒器 31〜50之火焰之輻射熱等加熱,而逐漸炼入為炫融玻璃 G2。以此獲得之熔融玻璃G2流向後方之後,自取出口 22 取出,並被供給至澄清槽。 熔解室10係藉由收容有使玻璃原料熔解所得之熔融玻璃 之熔解槽15、及覆蓋溶解槽15内之上部空間之頂棚16而形 成。熔解槽15及頂棚16係由煉磚等耐火物構成。 155915.doc 201141803 炫解至1 〇之大小並益特則pp ^ …、将別限疋’例如熔解室10之前後方 向尺寸X1為1 〇〜3 〇 m,較佳為 证砀10〜25 m。又,溶解室1〇之 寬度方向尺寸Y1為5〜i〇m。〗隹 進而’熔解室1〇之高度方向尺 寸Z1為3〜8 m。 對排氣口 24、25係用以將熔解室1〇内之燃燒後之氣體 向外部排氣者。1對排氣口 24、25配置於兩側壁13、14之 前後方向一端部,且配置於前壁“之附近。 配置於左側壁13之排氣口 24、及配置於右側㈣之排氣 口 25係隔著流路23而對向配置。若將靖排氣口 %、加 前後方向錯開配置’則會隔著流路23而左右非對稱地進行 排氣,因此難以控制熔融玻璃之溫度分佈。 排氣口 24、25之大小並無特別限定,例如排氣口 24、25 之刖後方向尺寸X2為1 m左右,排氣口 24、25之高度方向 尺寸Z2為1 m左右》 複數個燃燒器31〜50向炼解室内喷出火焰,將熔解室 ίο内之玻璃加熱而熔解。複數個燃燒器31〜5〇可連續地喷 出火焰,亦可斷續地噴出火焰。於斷續地喷出火焰之情形 時,複數個燃燒器31〜50可同時喷出火焰,亦可於不同之 時序喷出火焰。 複數個燃燒器3 1〜50係以不干擾彼此之火焰之方式配置 於兩側壁13、14。例如’配置於左側壁13之複數個燃燒器 31〜40、及配置於右側壁14之複數個燃燒器41〜5〇係隔著流 路23而對向配置。即,複數個燃燒器3丨〜咒係隔著流路23 而對稱配置。再者’複數個燃燒器3 1~50亦可隔著流路23 155915.doc 201141803 而交錯配置。 配置於左側壁13之複數個燃燒器31〜40沿流路23而於前 後方向上能以不等間距而排列,亦能以等間距而排列。配 置於右側壁14之複數個燃燒器41〜50亦相同。 複數個燃燒器3 1〜50喷出使燃料與氣體混合並燃燒所產 生之火焰。作為燃燒器3 1 ~50所使用之燃料,可使用例如 天然氣或管道煤氣等氣體燃料、重油等液體燃料。於使用 液體燃料之情形時,將液體燃燒喷霧成霧狀而使用。於複 數個燃燒器3 1〜50中,可使用同種燃料,亦可使用不同種 燃料。 一般而s,作為混合於燃料中之氣體,使用空氣及氧氣 之任一者。於使用有空氣之空氣燃燒之情形時,佔空氣之 約78體積%之氮氣無助於燃燒而被排氣至爐外。於使用有 氧氣之氧燃燒之情形時,與空氣燃燒之情形相比,排氣量 較/ ’故熱效率較高,c〇2排出量或N〇x排出量較少。 、作為混合於燃料中之氣體,亦有可能使用由空氣與氧氣 混《而^之混合氣體。該情形時,混合氣體中所佔氧氣之 比例:问’則燃燒後之氣體中所含之水分濃度越高,因此 =解室内之熔融破璃中溶存之水分量變多。㈣玻璃中溶 融玻璃;!^步驟中成為氣泡而上浮。因此,藉由使溶 ’合子之水分量最佳化而於澄清步驟中可促進熔融 玻璃内之氣泊 較少.的玻壤製品,’促進氣泡之上浮,從而可製造缺陷 作為'昆合於燃料中之氣體,於使用將空氣與氧氣 155915.doc 201141803 混合而成之混合氣體之情形時,與空氣燃燒之情形相比, 亦存在有NOx排出量變多之情形。詳細而言,於混合氣體 中之氧濃度未滿93體積%且超過25體積%之情形時,與空 氣燃燒之情形相比,NOx排出量變多。 相對於此’本實施形態中,作為燃燒器3丨〜5〇,係使用 喷出使燃料與空氣混合並燃燒所產生之火焰之空氣燃燒 器、及喷出使燃料與氧氣混合並燃燒所產生之火焰之氧燃 燒器。此處,所謂氧氣,係指氧濃度為93體積%以上之氣 體。如此,藉由使用空氣燃燒器與氧燃燒器而可抑制Ν〇χ 排出量之增加。 又,本實施形態中,複數個燃燒器31〜5〇每1小時之總燃 燒熱量Qa之30%以上(較佳為35%以上)9〇%以下(較佳為 87〇/。以下)係由氧燃燒器而產生。或者,熔解室⑺内之玻璃 加熱所使用之每1小時之總加熱量Qb之6〇%以上(較佳為 68〇/。以上)97%以下(較佳為95%以下)係由氧燃燒器而產 生。 此處,所謂熔解室10内之玻璃加熱所使用之每丨小時之 總加熱量Qb,係指複數個燃燒器小時之總燃燒熱 量Qa、與熔解室1〇内之燃燒後之氣體經由排氣口 24、25而 排出至熔解室1〇外部之每!小時之總排氣熱量Qc的差分 (Qa-QC)。該每丨小時之總排氣熱量Qc係根據每丨小時之排 氣量或排氣氣體之溫度等而計算。 以上述方式設定氧燃燒器相對於總燃燒熱量如之貢獻 率’藉此可抑制使用空氣燃燒器所導致的熱效率之降低或 155915.doc • 10- 201141803 c〇2排出量之增加'N〇x排出量之增加,由於可抑制 熱效率之降低,故熔解室10内之溫度易保持於較高溫。因 此:除納約玻璃製品外,亦特別適於高溶點之玻璃製品之 製造。作為此種高熔點之玻璃製品,可舉出例如液晶顯示 器用玻璃基板(所謂錢玻璃基板)。與—般的鈉㉝玻璃相 比’無鹼玻璃之熔點高達1 00»c以上。 然而,若將空氣燃燒器與氧燃燒器之兩者僅設置於炫解 爐中,則藉由設置於熔解室10之側壁13、14之排氣口 μ、 25之影響’有時難以充分調節溶解室1Q内之燃燒後之氣體 中所含之水分濃度。其結果有如下情形:充分調節溶解室 10内之熔融玻璃中溶存之水分量變得困難。 若熔融玻璃中溶存之水分量過少,則於澄清步驟 & 法充分促進熔融玻璃内之氣泡之上浮。另一方面,若熔融 玻璃中溶存之水分量過多,則於澄清步驟中,熔融玻璃内 會殘存有氣泡。而且,若溶融玻璃中溶存之水分量過多, 則一般可知於澄清步驟等中,當以鉑覆蓋熔融玻璃之流路 之内壁面之情形時,於熔融玻璃與鉑之界面上會產生氣 泡。 不過’熔解室10内之燃燒後之氣體具有朝排氣口 24、25 移動之傾向。 因此,本實施形態中,於自排氣口 24、25朝後方離開 0.6L以上(較佳為0.7L以上)之區域中,各設置有至少1個空 氣燃燒器及氧燃燒器。此處,L表示排氣口 24、25與前壁 11之間的前後方向上之距離L1及排氣口 24、25與後壁12之 155915.doc -11 - 201141803 間的前後方向上之距離L2中之最大距離(圖2、圖3所示之 例中為L2)。 如此,於自排氣口 24、25朝後方離開〇.6L以上之區域中 各設置有至少1個空氣燃燒器及氧燃燒器,因此可充分確 保空氣燃燒後之氣體與氧燃燒後之氣體混合之區域。藉 此,可充分確保可調節燃燒後之氣體令所含之水分濃度之 區域,可使熔解室10内之熔融玻璃中溶存之水分量於較大 範圍内可變。其結果為,可充分調節熔解室1〇内之熔融玻 璃中溶存之水分量,並於澄清步驟中,可促進熔融玻璃内 之氣泡之成長,促進氣泡之上浮,從而可製造缺陷較少的 玻璃製品。 再者’熔解室10内之熔融玻璃中溶存之水分量當然可根 據玻璃製品之組成或種類之變更而得以適當調節,亦可根 據爐壁之劣化、玻璃原料之批次之變更、燃料之批次之變 更等而得以適當調節。 溶解室10内之熔融玻璃中溶存之水分量之調節係藉由調 節空氣燃燒器與氧燃燒器每丨小時之燃燒熱量比而進行。 成為該調節之對象者主要為設置於自排氣口24、25朝後方 離開0.6L以上之區域中的燃燒器37〜4〇、47〜50。空氣燃燒 器相對於氧燃燒器之燃燒熱量比越高,則熔解室1〇内之燃 燒後之氣體中所含之水分濃度會變得越低,因此熔解室ι〇 内之熔融玻璃中溶存之水分量變少。 此處,設置於自1對排氣口 24、25朝後方離開〇.6L以上 之區域中的燃燒器37〜40、47〜50每1小時之燃燒熱量Qd之 155915.doc )2 201141803 5/〇以上95%以下(較佳為1〇%以上9〇%以下,更佳為15%以 上90%以下)係由空氣燃燒器而產生。 於未滿5%之情形時,熔解室1〇内之燃燒後之氣體中所 含之水分濃度過高,熔解室10内之熔融玻璃中溶存之水分 量過多。另一方面,於超過95%之情形時,熔解室10内之 燃燒後之氣體中所含之水分濃度過低,熔解室丨〇内之熔融 玻璃中溶存之水分量過少。 考慮到熔融玻璃中溶存之水分量與已製造之玻璃中之水 分量相同,故藉由已製造之玻璃中之β_〇Η之值(單位:/mm) 而表示。β-ΟΗ之值越大,則表示玻璃中之水分量越多ββ_ OH之值Β係藉由測定玻璃之板厚c及穿透率τ並將該測定結 果代入下式而計算。再者,於玻璃之穿透率之測定中,使 用一般的傅立葉轉換紅外分光光度計(FT IR)。Β = (l/C)l〇g1()(Tl/T2),Τ1 .參照波數^(^/(^的玻璃之穿透率 (單位:%),T2 :羥基吸收波數357〇/cm附近的玻璃之最小 穿透率(單位:%)。 例如’於無鹼玻璃之情形時,β_〇Η較佳為〇.25〜 〇.52/mm ’更佳為〇.3〜〇.5/mm,進而更佳為〇 35〜 〇.48/mm。 且說,於2個空氣燃燒器(例如,燃燒器38、4〇)之間, 較佳為设置至少1個氧燃燒器(例如,燃燒器39)。 若將2個空氣燃燒器彼此相鄰配置,則如上所述於空氣 燃燒中,與氧燃燒相比熱效率較低,故容易局部產生低溫 區域。 155915.doc •13· 201141803 再者’本實施形態中,形成為將排氣口 24 ' 25於流路23 之兩側壁13、14之各自上相對向地僅配置有1個之構成, 但亦可為將排氣口僅配置於流路之兩側壁之一方且僅配置 有1個之構成。 又’本實施形態中’將排氣口 24、25配置於側壁13、14 之前後方向一端部’並配置於前壁11之附近,但排氣口之 位置並無限制。例如’亦可將排氣口配置於後壁之附近。 又’亦可將排氣口設置於側壁之前後方向一端與前後方向 中央之中間。 (第2實施形態) 第2貫施形態係關於本發明之玻璃熔解爐。具體而言, 為將1對排氣口配置於側壁之前後方向中央之構成。即, 為將1對排氣口配置於前壁與後壁之間之中央之構成。 圖4係第2貫施形態之玻璃熔解爐之内部結構之側視圖。 圖5係第2實施形態之玻璃熔解爐之内部結構之俯視圖。於 圖5中,將各燃燒器之火焰之外緣以虛線包圍而表示。再 者,於圖4、圖5中,對於與圖2、圖3相同之構成標註相同 符號並省略其說明。 如圖4、圖5所示,熔解爐丨八係於熔解室1〇之前壁u具備 原料投入口 21,於熔解室1〇之後壁12具備取出口 22,於自 原料投入口 21到達取出口 22之流路23之側壁13、14具備複 數個燃燒器3 1A〜50A及1對排氣口 24A、25 A。 1對排氣口 24A、25A配置於兩側壁13、14之前後方向中 央,且配置於前壁U與後壁12之間之中央。配置於左側壁 155915.docThe maximum distance among the distance between the exhaust port and the rear wall in the front-rear direction is L, and at least 1 is provided in each of the regions from the exhaust port toward the front and/or the rear away from the 〇6L or more. Each of the above oxygen burners and the above air burners are disposed in the above-mentioned burners in the area! 5% or more and 95% or less of the total combustion heat of the hour is generated by the above air burner. Advantageous Effects of Invention According to the present invention, it is possible to provide a glass melting furnace capable of suppressing an increase in the amount of discharge and sufficiently adjusting the amount of water dissolved in the molten glass. This glass melting furnace is particularly effective in the case where the molten glass is sufficiently heated and the moisture content is lowered. [Embodiment] Hereinafter, embodiments for carrying out the invention will be described with reference to the drawings. In the respective drawings, the same components are denoted by the same reference numerals, and the description thereof will be omitted. (First Embodiment) Fig. 1 is a view showing the steps of a method for producing a glass product according to an embodiment of the present invention. Fig. 2 is a side elevational view showing the internal structure of the glass melting furnace of the first embodiment. Fig. 3 is a plan view showing the internal structure of the glass melting furnace of the first embodiment. In Fig. 3, the combustion zone of each burner (the outer edge of the flame of each burner) is surrounded by a broken line. As shown in FIG. 1, the manufacturing method of the glass article comprises: melting the glass raw material to obtain a melting step of the molten glass (sl〇〇); removing the bubbles of the molten glass to clarify the clarification step of the molten glass (sl〇2): and clarifying The subsequent molten glass 1559l5.doc 201141803 is formed into a specific shape forming step (S104). In these steps, the clarification step (S1G2) is a step of supplying the molten glass obtained in the series step to the clarification tank to float the bubbles in the molten glass and to remove them. As a method of promoting the bubbling of the bubbles, there is, for example, a method of degassing under reduced pressure and the like. The forming step (S1G4) is a step of forming the clarified (four) glass into a plate shape having a specific thickness. As a method of forming into a plate shape, there are known floating methods and melting methods, for example. The melting step (S100) is a step in which a plurality of raw materials are weighed and mixed, and the obtained glass raw materials are placed in a melting furnace and heated to a temperature corresponding to the type of the glass to be melted. As shown in Fig. 2 and Fig. 3, the melting furnace is provided on the upstream side of the melting chamber 10 of the molten glass raw material, and the raw material inlet port 21 is provided in the wall, and the downstream wall 12 has a take-out port 22 on the downstream side of the melting chamber 1 The two side walls 13, 14 of the flow path 23 from the raw material input port 21 to the take-out port 22 are provided with a plurality of burners 31 to 5A and a pair of exhaust ports 24'25. The two side walls 13, 14 extend in the front-rear direction. In the melting furnace 1, the glass raw material (1) fed from the raw material input port 21 and the molten glass G2 melted into 10 are heated by radiant heat from a flame of a plurality of burners 31 to 50, and gradually refined into Hyun glass G2. The molten glass G2 thus obtained flows backward, is taken out from the take-out port 22, and is supplied to the clarification tank. The melting chamber 10 is formed by accommodating a melting tank 15 for melting molten glass obtained by melting a glass raw material, and a ceiling 16 covering the upper space in the dissolution tank 15. The melting tank 15 and the ceiling 16 are made of a refractory such as a brick. 155915.doc 201141803 Hyun solution to the size of 1 并 and Yite pp ^ ..., will be limited to 疋 ' For example, the melting direction of the chamber 10 before and after the direction X1 is 1 〇 ~ 3 〇 m, preferably for the certificate 10~25 m . Further, the width direction dimension Y1 of the dissolution chamber 1 is 5 〜 i 〇 m.隹 进而 Further, the height direction dimension Z1 of the melting chamber is 3 to 8 m. The exhaust ports 24 and 25 are for exhausting the burned gas in the melting chamber 1 to the outside. The pair of exhaust ports 24 and 25 are disposed at one end in the front and rear directions of the side walls 13 and 14, and are disposed in the vicinity of the front wall. The exhaust port 24 disposed on the left side wall 13 and the exhaust port disposed on the right side (four) 25 is disposed opposite to each other via the flow path 23. If the % exhaust port and the front-rear direction are shifted, the exhaust flow is asymmetrically left and right across the flow path 23, so that it is difficult to control the temperature distribution of the molten glass. The size of the exhaust ports 24 and 25 is not particularly limited. For example, the size X2 of the exhaust ports 24 and 25 in the rear direction is about 1 m, and the dimension Z2 in the height direction of the exhaust ports 24 and 25 is about 1 m. The burners 31 to 50 discharge a flame into the refining chamber, and heat and melt the glass in the melting chamber ίο. The plurality of burners 31 to 5 〇 can continuously eject the flame, and the flame can be intermittently ejected. When the flame is ejected, a plurality of burners 31 to 50 can simultaneously eject the flame, and the flame can be ejected at different timings. The plurality of burners 3 1 to 50 are arranged in such a manner as to not interfere with each other's flames. Two side walls 13, 14 such as 'a plurality of disposed on the left side wall 13 The burners 31 to 40 and the plurality of burners 41 to 5 disposed on the right side wall 14 are disposed to face each other across the flow path 23. That is, the plurality of burners 3丨 to the spell are symmetrically sandwiched by the flow path 23. Further, the plurality of burners 3 1 to 50 may be alternately arranged via the flow path 23 155915.doc 201141803. The plurality of burners 31 to 40 disposed on the left side wall 13 are along the flow path 23 in the front-rear direction. The fuel cells can be arranged at equal intervals, and can be arranged at equal intervals. The plurality of burners 41 to 50 disposed on the right side wall 14 are also the same. The plurality of burners 3 1 to 50 are sprayed to mix the fuel and the gas and burn. The flame is generated. As the fuel used in the burners 3 to 50, a liquid fuel such as natural gas or pipeline gas, or a liquid fuel such as heavy oil can be used. In the case of using a liquid fuel, the liquid is burned and sprayed into a mist. In the plurality of burners 3 1 to 50, the same kind of fuel may be used, or different kinds of fuels may be used. Generally, as the gas mixed in the fuel, any one of air and oxygen may be used. When the air is burning, it takes up air About 78% by volume of nitrogen gas is not burned and is exhausted to the outside of the furnace. When using oxygen-burning oxygen, the amount of exhaust gas is higher than that of air combustion, so the thermal efficiency is higher, c 〇2 discharge or N〇x discharge is less. As a gas mixed in the fuel, it is also possible to use a mixture of air and oxygen. In this case, the proportion of oxygen in the mixed gas :[Q] The higher the concentration of water contained in the gas after combustion, the more the amount of water dissolved in the molten glass in the solution chamber is increased. (4) The molten glass in the glass is floated in the step; By optimizing the water content of the lysate, and in the clarification step, the glassy soil product in the molten glass can be promoted less, and the bubble is promoted to float, so that the defect can be produced as a 'Kunhe in the fuel. In the case of using a mixed gas in which air is mixed with oxygen 155915.doc 201141803, there is a case where the amount of NOx emission is increased as compared with the case of air combustion. In detail, when the oxygen concentration in the mixed gas is less than 93% by volume and exceeds 25% by volume, the amount of NOx emission is increased as compared with the case of air combustion. In contrast, in the present embodiment, as the burners 3 to 5, an air burner that ejects a flame generated by mixing fuel and air and burns, and a fuel that is mixed with fuel and oxygen are produced by combustion. Oxygen burner for the flame. Here, the term "oxygen" means a gas having an oxygen concentration of 93% by volume or more. Thus, an increase in the amount of enthalpy discharge can be suppressed by using an air burner and an oxygen burner. Further, in the present embodiment, 30% or more (preferably 35% or more) of the total combustion heat amount Qa per one hour of the plurality of burners 31 to 5 is 9% or less (preferably 87 Å/min or less). Produced by an oxygen burner. Alternatively, 6% or more (preferably 68 〇/. or more) and 97% or less (preferably 95% or less) of the total heating amount Qb per hour used for heating the glass in the melting chamber (7) is oxidized by oxygen. Produced by the device. Here, the total heating amount Qb per hour used for heating the glass in the melting chamber 10 means the total combustion heat amount Qa of a plurality of burner hours, and the combustion gas in the melting chamber 1〇 via the exhaust gas. The difference (Qa-QC) of the total exhaust heat amount Qc per hour of the outside of the melting chamber 1 is discharged to the outside of the melting chamber 1 and 25. The total exhaust heat amount Qc per hour is calculated based on the exhaust gas amount per hour or the temperature of the exhaust gas. Setting the contribution rate of the oxy-combustor relative to the total heat of combustion in the above manner can thereby suppress the decrease in thermal efficiency caused by the use of the air burner or 155915.doc • 10-201141803 c〇2 increase in discharge amount 'N〇x The increase in the discharge amount can suppress the decrease in thermal efficiency, so that the temperature in the melting chamber 10 is easily maintained at a relatively high temperature. Therefore, in addition to Nayano glass products, it is also particularly suitable for the manufacture of glass products with high melting point. As such a high melting point glass product, for example, a glass substrate for a liquid crystal display (so-called money glass substrate) can be mentioned. Compared with the general sodium 33 glass, the melting point of the alkali-free glass is up to 100»c or more. However, if both the air burner and the oxygen burner are disposed only in the dazzling furnace, it is sometimes difficult to sufficiently adjust by the influence of the exhaust ports μ, 25 provided on the side walls 13, 14 of the melting chamber 10. The concentration of water contained in the gas after combustion in the dissolution chamber 1Q. As a result, it is difficult to sufficiently adjust the amount of water dissolved in the molten glass in the dissolution chamber 10. If the amount of water dissolved in the molten glass is too small, the bubbles in the molten glass are sufficiently promoted to float upward in the clarification step & On the other hand, if the amount of water dissolved in the molten glass is too large, bubbles remain in the molten glass in the clarification step. In addition, when the amount of water dissolved in the molten glass is too large, it is generally known that bubbles are formed at the interface between the molten glass and the platinum when the inner wall surface of the flow path of the molten glass is covered with platinum in the clarification step or the like. However, the burned gas in the melting chamber 10 tends to move toward the exhaust ports 24, 25. Therefore, in the present embodiment, at least one air burner and an oxygen burner are provided in each of the regions which are separated from the exhaust ports 24 and 25 by 0.6 L or more (preferably 0.7 L or more). Here, L represents the distance L1 in the front-rear direction between the exhaust ports 24, 25 and the front wall 11, and the distance in the front-rear direction between the exhaust ports 24, 25 and the rear wall 12 of 155915.doc -11 - 201141803 The maximum distance in L2 (L2 in the example shown in Figures 2 and 3). In this way, at least one air burner and the oxygen burner are provided in each of the regions which are separated from the exhaust ports 24 and 25 toward the rear by 〇6L or more, so that the gas after the combustion of the air and the gas after the combustion of the oxygen can be sufficiently ensured. The area. As a result, it is possible to sufficiently ensure that the concentration of the water contained in the gas after the combustion is adjusted, and the amount of water dissolved in the molten glass in the melting chamber 10 can be varied over a wide range. As a result, the amount of water dissolved in the molten glass in the melting chamber 1 can be sufficiently adjusted, and in the clarification step, the growth of the bubbles in the molten glass can be promoted, and the floating of the bubbles can be promoted, whereby the glass having less defects can be produced. product. Further, the amount of water dissolved in the molten glass in the melting chamber 10 can be appropriately adjusted according to the composition or type of the glass product, or can be adjusted according to the deterioration of the furnace wall, the batch of the glass raw material, and the batch of the fuel. The second change can be appropriately adjusted. The adjustment of the amount of water dissolved in the molten glass in the dissolution chamber 10 is carried out by adjusting the ratio of the heat of combustion per hour of the air burner to the oxygen burner. The target to be adjusted is mainly the burners 37 to 4, 47 to 50 which are disposed in the region which is separated from the exhaust ports 24 and 25 by 0.6 L or more. The higher the combustion heat ratio of the air burner relative to the oxygen burner, the lower the concentration of water contained in the gas after combustion in the melting chamber 1 ,, so that the molten glass in the melting chamber is dissolved in the molten glass. The amount of water is reduced. Here, the burners 37 to 40, 47 to 50 in the region which is separated from the pair of exhaust ports 24 and 25 toward the rear by 〇.6L or more are 155915.doc per hour of heat combustion 2d 201141803 5/ 95% or less of the crucible (preferably 1% or more and 9% or less, more preferably 15% or more and 90% or less) is produced by an air burner. When the amount is less than 5%, the concentration of water contained in the gas after combustion in the melting chamber 1 is too high, and the amount of water dissolved in the molten glass in the melting chamber 10 is excessive. On the other hand, when it exceeds 95%, the concentration of water contained in the gas after combustion in the melting chamber 10 is too low, and the amount of water dissolved in the molten glass in the melting chamber is too small. It is considered that the amount of water dissolved in the molten glass is the same as the amount of water in the manufactured glass, and is represented by the value of β_〇Η (unit: /mm) in the manufactured glass. The larger the value of β-ΟΗ, the larger the amount of water in the glass. The value of ββ_ OH is calculated by measuring the plate thickness c and the transmittance τ of the glass and substituting the measurement result into the following formula. Further, in the measurement of the transmittance of glass, a general Fourier transform infrared spectrophotometer (FT IR) was used. Β = (l/C)l〇g1()(Tl/T2), Τ1. Reference wave number ^(^/(^ glass penetration rate (unit: %), T2: hydroxyl absorption wave number 357〇/ The minimum penetration rate of glass near cm (unit: %). For example, in the case of alkali-free glass, β_〇Η is preferably 〇.25~ 〇.52/mm 'better than 〇.3~〇 .5/mm, and more preferably 〇35~ 〇.48/mm. Furthermore, it is preferred to provide at least one oxygen burner between two air burners (for example, burners 38, 4). For example, the burner 39). If two air burners are arranged adjacent to each other, as described above, in the air combustion, the thermal efficiency is lower than that of the oxygen combustion, so that it is easy to locally generate a low temperature region. 155915.doc •13· In the present embodiment, in the present embodiment, only one of the exhaust ports 24' 25 is disposed opposite to each other on the side walls 13 and 14 of the flow path 23, but the exhaust port may be formed. Only one of the two side walls of the flow path is disposed, and only one of them is disposed. In the present embodiment, the exhaust ports 24 and 25 are disposed in front and rear end portions of the side walls 13 and 14 and disposed on the front wall. 11 In the vicinity, there is no restriction on the position of the exhaust port. For example, 'the exhaust port can also be placed near the rear wall. Also, the exhaust port can be placed in the middle of the rear side of the side wall and the center of the front and rear direction. (Second embodiment) The second embodiment is a glass melting furnace according to the present invention. Specifically, a pair of exhaust ports are disposed in the center in the rear direction of the side wall, that is, a pair of exhaust ports are disposed. Fig. 4 is a side view showing the internal structure of the glass melting furnace of the second embodiment. Fig. 5 is a plan view showing the internal structure of the glass melting furnace of the second embodiment. In Fig. 5, the outer edge of the flame of each of the burners is indicated by a broken line. The same components as those in Fig. 2 and Fig. 3 are denoted by the same reference numerals in Fig. 4 and Fig. 5, and the description thereof is omitted. 4. As shown in Fig. 5, the melting furnace is connected to the raw material inlet 21 before the melting chamber 1 is turned on, and the wall 12 is provided with the outlet 22 after the melting chamber 1 is turned, and the raw material inlet 21 reaches the outlet 22 The side walls 13, 14 of the flow path 23 are provided with a plurality of burners 3 1A ~50A and a pair of exhaust ports 24A and 25A. The pair of exhaust ports 24A and 25A are disposed at the center in the front-rear direction of the side walls 13 and 14, and are disposed at the center between the front wall U and the rear wall 12. Left side wall 155915.doc
S -14- 201141803 13之排氣口 24A、及配置於右側壁14之排氣口 25八係隔著 流路23而對向配置。 本貫施形態中,與第i實施形態同樣地,作為燃燒器 3 1A〜50A,係使用空氣燃燒器、及氧燃燒器。因此,與第 1實施形態同樣地’可抑制Ν〇χ排出量之增加。 又,本實施形態中,與第丨實施形態同樣地,複數個燃 燒器3 1Α-50Α每1小時之總燃燒熱量(^之3〇0/。以上(較佳為 350/❶以上)90%以下(較佳為87%以下)係由氧燃燒器而產 生。或者,熔解室10内之玻璃加熱所使用之每丨小時之總 加熱量Qb之60%以上(較佳為68%以上)97%以下(較佳為 95%以下)係由氧燃燒器而產生。 因此,與第1實施形態同樣地,可抑制使用空氣燃燒器 所導致的熱效率之降低或C〇2排出量之增加、n〇x排出量 之增加。又,由於可抑制熱效率之降低,故熔解室丨〇内之 溫度易保持於較高溫。 進而,本實施形態中’與第1實施形態同樣地,於自排 氣口 24A、25A朝後方離開0.6L以上(較佳為0.7L以上)之區 域中,各設置有至少1個空氣燃燒器及氧燃燒器。此處,L 表示排氣口 24A、25A與前壁11之間的前後方向上之距離 L3及排氣口 24A、25A與後壁12之間的前後方向上之距離 L4中之最大距離(於圖5所示之例中,L3=L4)。因此,與第 1實施形態同樣地’可確保可調節燃燒後之氣體中所含之 水分濃度之區域,可使熔解室10内之熔融玻璃中溶存之水 分量於較大範圍内可變。其結果為,可充分調節熔解室1〇 155915.doc 201141803 内之熔融玻璃中溶存之水分量,並於澄清步驟中,可促進 熔融玻璃内之氣泡之成長,促進氣泡之上浮,從而可製造 缺陷較少的玻璃製品。 熔解室ίο内之熔融玻璃中溶存之水分量之調節係藉由調 節空氣燃燒器與氧燃燒器每丨小時之燃燒熱量比而進行。 成為該調節之對象者主要為設置於自排氣σ24Α、25A朝 後方離開0.6L以上之區域中的燃燒器39八〜4〇A、 49A〜50A。空氣燃燒器相對於氧燃燒器之燃燒熱量比越 高,則熔解室10内之燃燒後之氣體中所含之水分濃度會變 得越低,因此熔解室10内之熔融玻璃中溶存之水分量變 少。 此處,設置於自排氣口 24A、25A朝後方離開〇.6L以上 之區域中的燃燒器39A〜40A、49A〜50A每1小時之燃燒熱 量Qd之5%以上95%以下(較佳為1 〇%以上以下,更佳為 150/〇以上90〇/〇以下)係由空氣燃燒器而產生。 於未滿5%之情形時,熔解室10内之燃燒後之氣體中所 3之水分濃度過咼,熔解室10内之溶融玻璃中溶存之水分 量過多。另一方面,於超過95。/〇之情形時,熔解室10内之 燃燒後之氣體中所含之水分濃度過低,溶解室1 〇内之溶融 玻璃中溶存之水分量過少。 再者’本實施形態中’形成為將排氣口 24A、25A於流 路23之兩側壁13、14之各自上相對向地僅配置有1個之構 成’但亦可為將排氣口僅配置於流路之兩側壁之一方且僅 配置有1個之構成。 155915.doc -16 - 201141803 又’本實施形態中’形成為於自排氣口 24A、25A朝後 方離開0.6L以上(較佳為0.7L以上)之區域中各設置有至少1 個空氣燃燒器及氧燃燒器的構成,但本發明並不限定於 此。亦可為例如於自排氣口 24A、25A朝前方離開〇.6L以上 (較佳為0.7L以上)之區域中各設置有至少1個空氣燃燒器及 氧燃燒器之構成,亦可將兩構成加以組合。 (第3實施形態) 第3實施形態係關於本發明之玻璃熔解爐。具體而言, 複數個燃燒器係隔著流路而交錯配置之構成者。 圖6係第3實施形態之玻璃熔解爐之内部結構之側視圖。 圖7係第3實施形態之玻璃熔解爐之内部結構之俯視圖。於 圖7中’將各燃燒器之火焰之外緣以虛線包圍而表示。再 者,於圖6、圖7中,對於與圖2、圖3相同之構成標註相同 符號並省略其說明。 如圖6、圖7所示,熔解爐⑶係於熔解室1〇B之前壁11]B 具備原料投入口 21B,於熔解室10B之後壁12B具備取出口 22B,於自原料投入口 21B到達取出口 22B之流路23B之側 壁13B、14B具備複數個燃燒器31B〜33B、41B〜42B及1對 排氣口 24B、25B。 溶解室10B之大小並無特別限定,例如熔解室1〇B之前 後方向尺寸X3為2〜5 m,熔解室10B之寬度方向尺寸Y3為 1〜3m,熔解室1〇B之高度方向尺寸以為丨^爪。 1對排氣口 24B、25B配置於兩側壁13B、14B之前後方向 端部,且配置於前壁11B之附近。配置於左側壁13B之排 155915.doc •17· 201141803 氣口 24B、及配置於右側壁14B之排氣口 25B係隔著流路 23B而對向配置。 排氣口 24B、25B之大小並無特別限定,例如排氣口 24B、25B之前後方向尺寸X4為0.3 m左右,排氣口 24B、 25B之高度方向尺寸Z4為0.2 m左右。 複數個燃燒器31B〜33B、41B〜42B隔著流路23B而交錯 配置。配置於左側壁13B之複數個燃燒器31B〜33B沿流路 2 3 B而於前後方向上排列。同樣地,配置於右側壁14 b之 複數個燃燒器41B〜42B沿流路23B而於前後方向上排列。 本實施形態中’與第1實施形態同樣地,作為燃燒器 31B〜33B、41B〜42B ’係使用空氣燃燒器及氧燃燒器。因 此,與第1實施形態同樣地’可抑制C〇2或NOx之排出量之 增加。 又,本實施形態中,與第1實施形態同樣地,複數個燃 燒器3 1B〜33B、41B〜42B每1小時之總燃燒熱量Qa之3〇%以 上(較佳為35%以上)9〇%以下(較佳為87%以下)係由氧燃燒 器而產生。或者,熔解室10B内之玻璃加熱所使用之每1小 時之總加熱量Qb之60%以上(較佳為68%以上)97°/。以下(較 佳為95%以下)係由氧燃燒器而產生。 因此,與第1實施形態同樣地,可抑制使用空氣燃燒器 所導致的熱效率之降低或c〇2排出量之增加、Ν〇χ排出量 之增加。又’由於可抑制熱效率之降低,故熔解室10Β内 之溫度易保持於較高溫。因此,適於高熔點之玻璃製品之 製造。 155915.doc 201141803 進而’本實施形態中,與第1實施形態同樣地,於自排 氣口 24B、25B朝後方離開0.6L以上(較佳為0.7L以上)之區 域中,各設置有至少1個空氣燃燒器及氧燃燒器。此處,L 表示排氣口 24B、25B與前壁11B之間的前後方向上之距離 L5及排氣口 24B、25B與後壁12B之間的前後方向上之距離 L6中之最大距離(圖7所示之例中為L6)。因此,與第1實施 形態同樣地’可充分確保可調節燃燒後之氣體中所含之水 分濃度之區域,可使熔解室10B内之熔融玻璃中溶存之水 分量於較大範圍内可變。其結果為,可充分調節熔解室 10B内之熔融玻璃中溶存之水分量,並於澄清步驟中,可 促進熔融玻璃内之氣泡之成長,促進氣泡之上浮,從而可 製造缺陷較少的玻璃製品。 熔解室10B内之熔融玻璃中溶存之水分量之調節係藉由 調節空氣燃燒器與氧燃燒器每丨小時之燃燒熱量比而進 行。成為該調節之對象者主要為設置於自排氣口 24B、 25B朝後方離開〇.6L以上之區域中的燃燒器33B、42B。空 氣燃燒器相對於氧燃燒器之燃燒熱量比越高,則熔解室 10B内之燃燒後之氣體中所含之水分濃度會變得越低,因 此熔解室10B内之熔融玻璃中溶存之水分量變少。 此處’設置於自排氣口24B、25B朝後方離開0.6L以上之 區域中的燃燒器33B、42B每1小時之燃燒熱量Qd之5%以上 95%以下(較佳為ι〇%以上9〇%以下,更佳為15%以上9〇%以 下)係由空氣燃燒器而產生。 於未滿5。/。之情形時’熔解室1〇B内之燃燒後之氣體中所 I559I5.doc •19· 201141803 含之水分濃度過高,溶解室1 〇B内之溶融玻璃中溶存之水 分量過多。另一方面,於超過95%之情形時,熔解室1〇B 内之燃燒後之氣體中所含之水分濃度過低,熔解室丨〇B内 之熔融玻璃中溶存之水分量過少。 以上’對本發明之第卜第3實施形態進行了說明,但本 發明並不限制於上述實施形態,在不脫離本發明之範圍内 可對上述實施形態進行各種變形及置換。 例如,如圖8所示之玻璃熔解爐1(:般,亦可於熔解室 10C之兩側壁13C、14C設置將熔解室i〇C區劃為2個室17、 18之縮頸部19。該情形時,後側之室18係用以調整熔融玻 璃之溫度之室,且於後側之室丨8之側壁未設置燃燒器。The exhaust port 24A of S-14-201141803 13 and the exhaust port 25 disposed on the right side wall 14 are disposed opposite to each other via the flow path 23. In the present embodiment, as in the i-th embodiment, an air burner and an oxygen burner are used as the burners 3 1A to 50A. Therefore, as in the first embodiment, the increase in the amount of enthalpy discharge can be suppressed. Further, in the present embodiment, as in the third embodiment, the total combustion heat per one hour of the plurality of burners 3 1 - 50 ( (3 〇 0 /. or more (preferably 350 / ❶ or more) 90%) The following (preferably 87% or less) is produced by an oxygen burner. Alternatively, 60% or more (preferably 68% or more) of the total heating amount Qb per hour used for heating the glass in the melting chamber 10 is 97. % or less (preferably 95% or less) is generated by an oxygen burner. Therefore, similarly to the first embodiment, it is possible to suppress a decrease in thermal efficiency or an increase in the amount of C〇2 discharged by using an air burner, n. In addition, since the decrease in the heat efficiency is suppressed, the temperature in the melting chamber is easily maintained at a relatively high temperature. Further, in the present embodiment, the self-venting port is the same as in the first embodiment. 24A and 25A are provided with at least one air burner and an oxygen burner in an area of 0.6 L or more (preferably 0.7 L or more) toward the rear. Here, L denotes an exhaust port 24A, 25A and a front wall 11 The distance L3 between the front and rear directions and between the exhaust ports 24A, 25A and the rear wall 12 The maximum distance in the distance L4 in the front-rear direction (in the example shown in Fig. 5, L3 = L4). Therefore, as in the first embodiment, it is possible to ensure the concentration of water contained in the gas after the combustion can be adjusted. In the region, the amount of water dissolved in the molten glass in the melting chamber 10 can be varied within a wide range. As a result, the amount of water dissolved in the molten glass in the melting chamber 1 155915.doc 201141803 can be sufficiently adjusted, and In the clarification step, the growth of the bubbles in the molten glass is promoted, and the floating of the bubbles is promoted, so that the glass product having less defects can be produced. The adjustment of the amount of water dissolved in the molten glass in the melting chamber is regulated by adjusting the air. The ratio of the heat of combustion to the oxygen burner per hour is set. The target of the adjustment is mainly a burner 39 ~4〇A which is disposed in an area of 0.6L or more from the exhaust σ24Α, 25A toward the rear. 49A to 50A. The higher the combustion heat ratio of the air burner with respect to the oxygen burner, the lower the concentration of water contained in the gas after combustion in the melting chamber 10, and thus the melting in the melting chamber 10. The amount of water dissolved in the glass is reduced. Here, the burners 39A to 40A and 49A to 50A which are disposed in the region which is separated from the exhaust ports 24A and 25A toward the rear by 〇6L or more are 5% of the heat of combustion Qd per hour. 95% or less (preferably 1% or less, more preferably 150/〇 or more 90〇/〇) is produced by an air burner. In the case of less than 5%, the combustion in the melting chamber 10 The concentration of water in the gas 3 is too high, and the amount of water dissolved in the molten glass in the melting chamber 10 is excessive. On the other hand, in the case of exceeding 95%, the gas in the combustion chamber 10 is burned. If the concentration of water contained is too low, the amount of water dissolved in the molten glass in the dissolution chamber 1 is too small. Further, in the present embodiment, the exhaust ports 24A and 25A are formed so that only one of the two side walls 13 and 14 of the flow path 23 is disposed to face each other, but the exhaust port may be formed only. It is disposed on one of the two side walls of the flow path and is configured by only one of them. 155915.doc -16 - 201141803 Further, in the present embodiment, at least one air burner is provided in each of the regions which are separated from the exhaust ports 24A and 25A by 0.6 L or more (preferably 0.7 L or more). The configuration of the oxygen burner is not limited to this. For example, at least one air burner and an oxygen burner may be provided in each of the regions which are separated from the exhaust ports 24A and 25A by a distance of 6 liters or more (preferably 0.7 L or more). The composition is combined. (Third Embodiment) A third embodiment relates to a glass melting furnace of the present invention. Specifically, a plurality of burners are arranged in a staggered arrangement via a flow path. Fig. 6 is a side view showing the internal structure of a glass melting furnace according to a third embodiment. Fig. 7 is a plan view showing the internal structure of a glass melting furnace according to a third embodiment. In Fig. 7, 'the outer edge of the flame of each burner is surrounded by a broken line. In FIGS. 6 and 7, the same components as those in FIGS. 2 and 3 are denoted by the same reference numerals, and their description will be omitted. As shown in Fig. 6 and Fig. 7, the melting furnace (3) is provided in the melting chamber 1B before the wall 11] B is provided with the raw material input port 21B, and after the melting chamber 10B, the wall 12B is provided with the take-out port 22B, and is taken from the raw material input port 21B. The side walls 13B and 14B of the flow path 23B of the outlet 22B are provided with a plurality of burners 31B to 33B, 41B to 42B, and a pair of exhaust ports 24B and 25B. The size of the dissolution chamber 10B is not particularly limited. For example, the dimension X3 in the front and rear directions of the melting chamber 1B is 2 to 5 m, and the dimension Y3 in the width direction of the melting chamber 10B is 1 to 3 m, and the dimension in the height direction of the melting chamber 1B is considered to be丨^ claws. The pair of exhaust ports 24B and 25B are disposed in front and rear end portions of the side walls 13B and 14B, and are disposed in the vicinity of the front wall 11B. The exhaust port 25B disposed on the left side wall 13B 155915.doc • 17· 201141803 and the exhaust port 25B disposed on the right side wall 14B are disposed to face each other across the flow path 23B. The size of the exhaust ports 24B and 25B is not particularly limited. For example, the front and rear direction dimensions X4 of the exhaust ports 24B and 25B are about 0.3 m, and the height direction dimension Z4 of the exhaust ports 24B and 25B is about 0.2 m. The plurality of burners 31B to 33B and 41B to 42B are alternately arranged via the flow path 23B. The plurality of burners 31B to 33B disposed on the left side wall 13B are arranged in the front-rear direction along the flow path 2 3 B. Similarly, the plurality of burners 41B to 42B disposed on the right side wall 14b are arranged in the front-rear direction along the flow path 23B. In the present embodiment, as in the first embodiment, an air burner and an oxygen burner are used as the burners 31B to 33B and 41B to 42B'. Therefore, as in the first embodiment, the increase in the discharge amount of C〇2 or NOx can be suppressed. Further, in the present embodiment, as in the first embodiment, the plurality of burners 3 1B to 33B and 41B to 42B have a total combustion heat amount Qa of 3% or more (preferably 35% or more) per hour. % or less (preferably 87% or less) is produced by an oxygen burner. Alternatively, 60% or more (preferably 68% or more) of the total heating amount Qb per one hour used for heating the glass in the melting chamber 10B is 97 °/. The following (more preferably 95% or less) is produced by an oxygen burner. Therefore, similarly to the first embodiment, it is possible to suppress a decrease in thermal efficiency caused by the use of an air burner, an increase in the amount of c〇2 discharged, and an increase in the amount of helium discharged. Further, since the decrease in thermal efficiency can be suppressed, the temperature in the melting chamber 10 is easily maintained at a relatively high temperature. Therefore, it is suitable for the manufacture of glass products having a high melting point. In the same manner as the first embodiment, at least 1 in each of the regions from the exhaust ports 24B and 25B that are separated by 0.6 L or more (preferably 0.7 L or more) from the exhaust ports 24B and 25B are provided. An air burner and an oxygen burner. Here, L represents the distance L5 in the front-rear direction between the exhaust ports 24B, 25B and the front wall 11B and the maximum distance L6 in the front-rear direction between the exhaust ports 24B, 25B and the rear wall 12B (Fig. In the example shown in Figure 7, it is L6). Therefore, in the same manner as in the first embodiment, the region in which the concentration of water contained in the gas after combustion can be sufficiently ensured can be made such that the amount of water dissolved in the molten glass in the melting chamber 10B can be varied over a wide range. As a result, the amount of water dissolved in the molten glass in the melting chamber 10B can be sufficiently adjusted, and in the clarification step, the growth of the bubbles in the molten glass can be promoted, and the floating of the bubbles can be promoted, thereby making it possible to manufacture a glass product having fewer defects. . The adjustment of the amount of moisture dissolved in the molten glass in the melting chamber 10B is carried out by adjusting the combustion heat ratio of the air burner to the oxygen burner every hour. The person to be the target of the adjustment is mainly the burners 33B and 42B provided in the region which is separated from the exhaust ports 24B and 25B by 〇.6L or more. The higher the ratio of the heat of combustion of the air burner to the oxygen burner, the lower the concentration of water contained in the gas after combustion in the melting chamber 10B, so that the amount of water dissolved in the molten glass in the melting chamber 10B becomes less. Here, the burners 33B and 42B provided in the region of 0.6 L or more from the exhaust ports 24B and 25B are 5% or more and 95% or less of the combustion heat amount Qd per hour (preferably ι 〇 % or more 9) 〇% or less, more preferably 15% or more and 9% or less) is produced by an air burner. Not less than 5. /. In the case of the combustion gas in the melting chamber 1〇B, I559I5.doc •19· 201141803 The water concentration is too high, and the amount of water dissolved in the molten glass in the dissolution chamber 1 〇B is excessive. On the other hand, when it exceeds 95%, the concentration of water contained in the gas after combustion in the melting chamber 1B is too low, and the amount of water dissolved in the molten glass in the melting chamber B is too small. The third embodiment of the present invention has been described above, but the present invention is not limited to the above-described embodiments, and various modifications and changes can be made to the above-described embodiments without departing from the scope of the invention. For example, as shown in Fig. 8, the glass melting furnace 1 (in general, the narrowing of the melting chamber i 〇 C into the two chambers 17 and 18 may be provided in the side walls 13C and 14C of the melting chamber 10C. At the time, the chamber 18 on the rear side is a chamber for adjusting the temperature of the molten glass, and the burner is not provided on the side wall of the chamber 8 on the rear side.
又,如圖9所示之玻璃熔解爐1]〇般,亦可於熔解室i〇DMoreover, as shown in FIG. 9, the glass melting furnace 1] can also be used in the melting chamber i〇D
之兩側J 13D、14D设置原料投人σ 2 1D,並將排氣口 24D 設置於前壁再者,排氣D24D亦可設置於前壁ud及/ 或後壁12D上。 又作為加熱熔融玻璃之方法,除利用上述燃燒器喷出 之火焰之輻射熱的方法外,亦可併用將熔融玻璃直接通電 加熱之方法。 又,本發明之空氣燃燒器之燃料中混合之氣體較佳為空 氣仁如上所述於出量不變多的程度下,具體而言 若燃料中混合之氣體中之氧為25體積%以下,則除空氣外 可混合氧氣。 再者,於熔解室之側壁上,較佳為設置用以進行玻璃熔 融狀况確邁之觀察用窗(未圓示),觀察用窗之擋板為了提 155915.doc 201141803 尚上下開閉時之密閉性而務傾斜地設置為佳β 實施例 以下,透過實施例而具體說明本發明,但本發明並非藉 由以下實施例而受到限定。 (例1〜10) 例1〜10(表1、2)中,藉由計算而求出使用圖2、圖3所示 之玻璃熔解爐製造之玻璃中之β_〇Η(單位:/mm)。Ρ_〇Η為 表示玻璃中之水分量之指標,其係指Ρ_〇Η越大,則玻璃中 之水分量越多。例2、4〜6、10為實施例,例i、3、7〜9為 比較例。 此處,對β-ΟΗ之計算方法進行簡單說明。首先,根據 由各燃燒器燃燒之燃料及氣體之組成等,計算燃燒後之氣 體中所含之水分濃度等。其次’考慮燃燒後之氣體朝排氣 口流動,計算熔解室内之環境中之水分濃度之分佈。然 後,根據水分濃度之分佈及熔融玻璃之平均流速,計算最 終擴散至熔融玻璃中之水分量,並換算成製造後之玻璃中 所含之β-ΟΗ。 於各例1〜10中,分別將熔解室之前後方向尺寸XI設定 為25 m’祕解室10之寬度方向尺寸Υ1設定為10m,將溶 解至10之问度方向尺寸Z1設定為8 m。又將熔解室⑺内 之熔融玻璃之體積設定為3〇〇 m3,將每H、時投入至熔解 室10内之玻璃原料(即,自熔解室1〇#1小時取出之溶融玻 璃)之體積設定為K25 m3e進而,將排氣口 24、25之前後 方向尺寸X2設定為1 m,將排氣口 24、25之高度方向尺寸 1559l5.doc -21· 201141803 "又与m。又,於左側壁13上,將前壁丨丨與排氣口 24 之間的前後方向上之距離L1設定為2 m,將自排氣口 24至 各燃燒器3 1〜40為止的各自之前後方向上之距離設定為2 mxN(N為1〜1〇之自然數),將排氣口 24與燃燒器4〇之間的 刖後方向上之距離設定為2〇 m。同樣地,於右側壁丨4上, 亦設定排氣口 25及複數個燃燒器41〜5〇之配置。 而且’於各例i、2、4、5、7〜10中,將複數個燃燒器 31〜50各自之每!小時之燃燒熱量設定為相同。另一方面, 於例3申,將複數個氧燃燒器各自之每丨小時之燃燒熱量設 定為相同’將複數個空氣燃燒器各自之每1小時之燃燒熱 量設定為相同’並且將各空氣燃燒器每1小時之燃燒熱量 設定為小於各氧燃燒器每1小時之燃燒熱量。又,例6中, 將複數個氧燃燒器各自之每1小時之燃燒熱量設定為相 同’將複數個空氣燃燒器各自之每1小時之燃燒熱量設定 為相同’並且將各空氣燃燒器每1小時之燃燒熱量設定為 大於各氧燃燒器每1小時之燃燒熱量。再者,作為例1、9 之燃燒器31〜50,係僅使用氧燃燒器,作為例2-8、10之燃 燒器31~50,係使用氧燃燒器與空氣燃燒器。 於表1、2中,C02排出量之單位Nm3表示標準狀態 (〇°C,1氣壓)下之體積(表3、表4亦相同)。表1、2中,顯 示有空氣燃燒器之No.(編號),故省略氧燃燒器之No.(表 3、表4亦相同)。 155915.doc -22- 201141803 [表l] 例1 例2 例3 例4 例5 氧燃燒器之燃料 天然氣 天然氣 天然氣 天然氣 天然氣 空氣燃燒器之No_ - 38、48 38、48 38 32、38、 42、48 空氣燃燒器之燃料 - 天然氣 天然氣 天然氣 天然氣 每1小時之總燃燒熱量Qa(kWh) 10000 12200 10200 11100 14300 氧燃燒器相對於Qa之貢獻率(%) 100 74 91 87 56 每1小時之總加熱量Qb(kWh) 7300 7300 7300 7300 7300 氧燃燒器相對於Qb之貢獻率(%) 100 90 99 95 80 每1小時之C02排出量(Nm3/h) 1050 1250 1050 1150 1475 距離L(m) 22 22 22 22 22 排氣口與離排氣口最遠的空氣燃燒器 之間的前後方向上之距離La(m) - 16 16 16 16 La/L - 0.73 0.73 0.73 0.73 空氣燃燒器相對於特定區域之每1小 時之總燃燒熱量Qd的貢獻率(%) - 51 9 20 51 p-OH(mm') 0.50 0.39 0.47 0.42 0.37 [表2] 例6 例7 例8 例9 例10 氧燃燒器之燃料 天然氣 天然氣 天然氣 重油 重油 空氣燃燒器之No. 38、48 32'42 3 卜 32、 41 > 42 - 38、48 空氣燃燒器之燃料 天然氣 天然氣 天然氣 - 重油 每1小時之總燃燒熱量Qa(kWh) 17800 12200 14300 9700 11800 氧燃燒器相對於Qa之貢獻率(%) 36 74 56 100 74 每1小時之總加熱量Qb(kWh) 7300 7300 7300 7300 7300 氧燃燒器相對於Qb之貢獻率(%) 64 90 80 100 90 . 每1小時之C02排出量(Nm3/h) 1830 1250 1475 1350 1500 距離L(m) 22 22 22 22 22 排氣口與離排氣口最遠的空氣燃燒器 之間的前後方向上之距離La(m) 16 4 2 - 16 La/L 0.73 0.18 0.09 - 0.73 空氣燃燒器相對於特定區域之每1小 時之總燃燒熱量Qd的貢獻率(%) 84 0 0 - 51 β-ΟΗΟηηι·1) 0.32 0.47 0.46 0.40 0.32 •23- 155915.doc 201141803 如根據表1、2所理解,對於燃料為天然氣之例1〜8,於 例2、4〜6中,於自排氣口 24、25朝後方離開〇.6L以上之區 域中’各設置有至少1個空氣燃燒器及氧燃燒器,與例1之 情形相比,玻璃中之β-OH下降10%以上。又,對於燃料為 重油之例9、1 〇,於例1 0中,於自排氣口 24、25朝後方離 開0.6L以上之區域中’各設置有至少1個空氣燃燒器及氧 燃燒器’與例9之情形相比,玻璃中之β_〇Η下降1 〇。/0以 上。若下降10%以上’則使空氣燃燒器與氧燃燒器每1小 時之燃燒熱量比發生變化,藉此可充分調整β_〇Η。因此, 於例2、4〜6、1 〇中’藉由調節空氣燃燒器與氧燃燒器每i 小時之燃燒熱量比而可充分調節熔解室1〇内之熔融玻璃中 f谷存之水分量。 另一方面’於例7、8中,於自排氣口 24、25朝後方離開 0.6L以上之區域中,未設置空氣燃燒器,因而相對於例 1 ’ β-ΟΗ未下降1〇%以上。由此而判定,即便調節空氣燃 燒器與氧燃燒器每1小時之燃燒熱量比,亦難以充分調節 炫解室10内之熔融玻璃中溶存之水分量。 又’例3中’與例2同樣地,於自排氣口 24、25朝後方離 開0.6L以上之區域中,各設置有至少1個空氣燃燒器及氧 燃燒器’但與例2不同,熔解室内之玻璃加熱所使用之每i 小時之總加熱量Qb之99%係由氧燃燒器而產生。因此,例 3中’玻璃中之β·〇Η相對於例1並未降低10〇/〇以上。由此而 判疋’例3中’難以充分降低熔解室丨〇内之溶融玻璃中溶 存之水分量。 155915.docThe two sides J 13D, 14D are provided with the raw material investment σ 2 1D, and the exhaust port 24D is disposed on the front wall. The exhaust gas D24D may also be disposed on the front wall ud and/or the rear wall 12D. Further, as a method of heating the molten glass, in addition to the method of using the radiant heat of the flame sprayed from the burner, a method of directly heating and heating the molten glass may be used. Moreover, it is preferable that the gas mixed in the fuel of the air burner of the present invention is such that the amount of air is not changed as much as described above, and specifically, if the amount of oxygen in the gas mixed in the fuel is 25% by volume or less, Oxygen can be mixed in addition to air. Furthermore, on the side wall of the melting chamber, it is preferable to provide a viewing window for the glass melting condition (not shown), and the baffle for the observation window is opened and closed for the purpose of raising the 155915.doc 201141803. The present invention is specifically described by way of examples, but the present invention is not limited by the following examples. (Examples 1 to 10) In Examples 1 to 10 (Tables 1 and 2), β_〇Η (unit: /mm) in the glass produced by using the glass melting furnace shown in Fig. 2 and Fig. 3 was calculated by calculation. ). Ρ_〇Η is an indicator of the amount of water in the glass. It means that the larger the Ρ_〇Η, the more water in the glass. Examples 2, 4 to 6, and 10 are examples, and examples i, 3, and 7 to 9 are comparative examples. Here, the calculation method of β-ΟΗ is briefly described. First, the concentration of water contained in the gas after combustion or the like is calculated based on the composition of the fuel and gas burned by each burner. Second, consider the flow of the burned gas toward the exhaust port to calculate the distribution of the water concentration in the environment inside the melting chamber. Then, based on the distribution of the water concentration and the average flow velocity of the molten glass, the amount of water which is finally diffused into the molten glass is calculated and converted into β-ΟΗ contained in the glass after the production. In each of Examples 1 to 10, the dimension XI in the front and rear directions of the melting chamber was set to 25 m. The dimension Υ1 in the width direction of the secret chamber 10 was set to 10 m, and the dimension Z1 in the direction of dissolution to 10 was set to 8 m. Further, the volume of the molten glass in the melting chamber (7) is set to 3 〇〇m3, and the volume of the glass raw material (i.e., the molten glass taken out from the melting chamber 1 〇 #1 hour) is supplied to the melting chamber 10 every H and hour. It is set to K25 m3e, and the front and rear direction dimensions X2 of the exhaust ports 24 and 25 are set to 1 m, and the height direction dimensions of the exhaust ports 24 and 25 are 1559l5.doc -21·201141803 " Further, on the left side wall 13, the distance L1 in the front-rear direction between the front wall 丨丨 and the exhaust port 24 is set to 2 m, and each of the self-venting ports 24 to the respective burners 3 1 to 40 The distance in the rear direction is set to 2 mxN (N is a natural number of 1 to 1 )), and the distance in the rear direction between the exhaust port 24 and the burner 4 is set to 2 〇 m. Similarly, on the right side wall 4, the arrangement of the exhaust port 25 and the plurality of burners 41 to 5 are also set. Further, in each of the examples i, 2, 4, 5, and 7 to 10, each of the plurality of burners 31 to 50 is each! The heat of combustion for the hour is set to be the same. On the other hand, in Example 3, the combustion heat per hour of each of the plurality of oxygen burners is set to be the same 'the combustion heat per hour of each of the plurality of air burners is set to be the same' and the respective air is burned The heat of combustion per hour is set to be less than the heat of combustion per hour of each oxygen burner. Further, in Example 6, the heat of combustion per one hour of each of the plurality of oxygen burners is set to be the same 'the combustion heat per hour of each of the plurality of air burners is set to be the same' and each of the air burners is 1 The heat of combustion for hours is set to be greater than the heat of combustion per hour of each oxygen burner. Further, as the burners 31 to 50 of Examples 1 and 9, only an oxygen burner was used, and as the burners 31 to 50 of Examples 2-8 and 10, an oxygen burner and an air burner were used. In Tables 1 and 2, the unit Nm3 of the C02 discharge amount indicates the volume in the standard state (〇°C, 1 atm) (the same applies to Table 3 and Table 4). In Tables 1 and 2, the No. (number) of the air burner is shown, so the No. of the oxygen burner is omitted (the same applies to Table 3 and Table 4). 155915.doc -22- 201141803 [Table l] Example 1 Example 2 Example 3 Example 4 Example 5 Oxygen burner fuel Natural gas Natural gas Natural gas Natural gas air burner No_ - 38, 48 38, 48 38 32, 38, 42 48 Air Burner Fuel - Natural Gas Natural Gas Natural Gas Burning Heat per 1 hour Qa(kWh) 10000 12200 10200 11100 14300 Contribution Rate of Oxygen Burner to Qa (%) 100 74 91 87 56 Total Heating per 1 hour Qb (kWh) 7300 7300 7300 7300 7300 Contribution rate of oxygen burner to Qb (%) 100 90 99 95 80 C02 discharge per hour (Nm3/h) 1050 1250 1050 1150 1475 Distance L(m) 22 22 22 22 22 Distance in the front-rear direction between the exhaust port and the air burner farthest from the exhaust port La(m) - 16 16 16 16 La/L - 0.73 0.73 0.73 0.73 Air burner relative to specific area Contribution rate (%) of total heat of combustion Qd per hour - 51 9 20 51 p-OH(mm') 0.50 0.39 0.47 0.42 0.37 [Table 2] Example 6 Example 7 Example 8 Example 9 Example 10 Oxygen burner Fuel Natural Gas Natural Gas Heavy Oil Heavy Oil Air Burner No. 38, 48 32'42 3 32, 41 > 42 - 38, 48 Air Burner Fuel Natural Gas Natural Gas - Total Combustion Heat per 1 hour of Heavy Oil Qa(kWh) 17800 12200 14300 9700 11800 Contribution Rate of Oxygen Burner to Qa (%) 36 74 56 100 74 Total heating per hour Qb (kWh) 7300 7300 7300 7300 7300 Contribution rate of oxygen burner to Qb (%) 64 90 80 100 90 . C02 emissions per hour (Nm3/h) 1830 1250 1475 1350 1500 Distance L(m) 22 22 22 22 22 Distance in the front-rear direction between the exhaust port and the air burner farthest from the exhaust port La(m) 16 4 2 - 16 La/L 0.73 0.18 0.09 - 0.73 Contribution rate of air burner to total combustion heat Qd per hour for a specific area (%) 84 0 0 - 51 β-ΟΗΟηηι·1) 0.32 0.47 0.46 0.40 0.32 •23- 155915.doc 201141803 As understood from Tables 1 and 2, in the examples 1 to 8 in which the fuel is natural gas, in the examples 2 and 4 to 6, in the region which is separated from the exhaust ports 24 and 25 toward the rear by 〇.6L or more, each of them is provided with at least 1 For the air burner and the oxygen burner, the β-OH in the glass was reduced by more than 10% compared with the case of Example 1. Further, in the case of the example 9 and 1 in which the fuel is heavy oil, in the example 10, at least one air burner and the oxygen burner are provided in each of the regions which are separated from the exhaust ports 24 and 25 by 0.6 L or more. 'Compared with the case of Example 9, β_〇Η in the glass decreased by 1 〇. Above /0. If it is lowered by 10% or more, the combustion heat ratio per hour of the air burner and the oxygen burner is changed, whereby β_〇Η can be sufficiently adjusted. Therefore, in Examples 2, 4 to 6, and 1 ', the moisture content of the f-storage in the molten glass in the melting chamber 1 can be sufficiently adjusted by adjusting the ratio of the combustion heat per hour of the air burner to the oxygen burner. . On the other hand, in Examples 7 and 8, in the region where the exhaust ports 24 and 25 were separated by 0.6 L or more from the rear, no air burner was provided, so that the sample 1 'β-ΟΗ did not fall by 1% or more. . From this, it was judged that even if the ratio of the heat of combustion of the air burner to the oxygen burner per hour was adjusted, it was difficult to sufficiently adjust the amount of water dissolved in the molten glass in the escapement chamber 10. In the same manner as in the example 2, at least one air burner and the oxygen burner are provided in each of the regions which are separated from the exhaust ports 24 and 25 by 0.6 L or more, but different from the example 2, 99% of the total heating amount Qb per hour used for heating the glass in the melting chamber is generated by an oxygen burner. Therefore, the β·〇Η in the glass in Example 3 was not lowered by 10 Å/〇 or more with respect to Example 1. From this, it was judged that in Example 3, it was difficult to sufficiently reduce the amount of water dissolved in the molten glass in the melting chamber. 155915.doc
S •24· 201141803 (例11〜12) 例11〜12(表3)中,藉由上述計算而求出使用圖4、圖5所 示之玻璃炼解爐製造之玻璃中之β-ΟΗ(單位:/mm)。例12 為實施例,例11為比較例。 於各例11〜12中,係將排氣口 24A、25A配置於側壁13、 14之前後方向中央,除此以外,將熔解室之大小、排氣口 之大小、排氣口與各燃燒器之間的前後方向上之距離等與 例1〜10同樣地設定。於各例11〜12中,將複數個燃燒器 31A〜50A各自之每1小時之燃燒熱量設定為相同。再者, 作為例11之燃燒器3 1A〜50A,係僅使用氧燃燒器,作為例 12之燃燒器31A〜50A,係使用氧燃燒器與空氣燃燒器。 [表3] 例11 例12 氧燃燒器之燃料 天然氣 天然氣 空氣燃燒器之No. - 39A、49A 空氣燃燒器之燃料 - 天然氣 每1小時之總燃燒熱量Qa(kWh) 10000 12200 氧燃燒器相對於Qa之貢獻率(%) 100 74 每1小時之總加熱量Qb(kWh) 7300 7300 氧燃燒器相對於Qb之貢獻率(%) 100 90 每1小時之C02排出量(Nm3/h) 1050 1250 距離L(m) 12 12 排氣口與離排氣口最遠的空氣燃燒器之間的前後方向上之距離 La(m) - 8 La/L - 0.67 空氣燃燒器相對於特定區域之每1小時之總燃燒熱量Qd的貢獻 率(%) - 51 P-OH(mm'') 0.51 0.45 如根據表3所理解,例12中,於自排氣口 24A、25A朝後 155915.doc -25- 201141803 方離開0.6L以上之區域中,各設置有至個空氣燃燒器 及氧燃燒器,與例11之情形相比,玻璃中之p_〇H下降1〇% 以上。由此而判定,例12中,藉由調節空氣燃燒器與氧燃 燒器每1小時之燃燒熱量比而可充分調節熔解室1〇内之炫 融玻璃中溶存之水分量。 (例13〜14) 例13〜14(表4)中,藉由上述計算而求出使用圖6、圖7所 示之玻璃熔解爐製造之玻璃中之β_0Η(單位:/mm)。例14 為實施例,例13為比較例。 於各例13〜14中,將熔解室10B之前後方向尺寸幻設定 為3 m,將熔解室10B之寬度方向尺寸γ3設定為2 m,將熔 解室10B之高度方向尺寸23設定為2 me又,將熔解室i〇b 内之熔融玻璃之體積設定為4.5 m3,將每!小時投入至熔解 至10B内之玻璃原料(即,自炼解室時取出之炼融 玻璃)之體積设定為〇 〇4 m3 〇進而’將排氣口 24b、25B之 前後方向尺寸X4設定為〇.3 m,將排氣口 24B、25B之高度 方向尺寸Z4設定為0 3 m。又,於左側壁nB,分別將前壁 1 與排氣口 24B之間的前後方向上之距離l5設定為〇.2 m ’將排氣口 24B與燃燒器31B之間的前後方向上之距離設 疋為〇.3 m ’將排氣口 24B與燃燒器32B之間的前後方向上 之距離設定為10 m,將排氣口 24B與燃燒器33B之間的前 後方向上之距離設定為2 〇 m。另一方面,於右側壁1, 分別將前壁11B與排氣口 25B之間的前後方向上之距離L5 设定為〇·2 m ’將排氣口 25B與燃燒器41B之間的前後方向 155915.docS • 24· 201141803 (Examples 11 to 12) In Examples 11 to 12 (Table 3), β-ΟΗ in the glass produced by using the glass refining furnace shown in Figs. 4 and 5 was obtained by the above calculation. Unit: /mm). Example 12 is an example, and Example 11 is a comparative example. In each of the examples 11 to 12, the exhaust ports 24A and 25A are disposed in the center in the front and rear directions of the side walls 13 and 14, and the size of the melting chamber, the size of the exhaust port, the exhaust port, and each burner are used. The distance between the front and rear directions and the like are set in the same manner as in the examples 1 to 10. In each of Examples 11 to 12, the heat of combustion per one hour of each of the plurality of burners 31A to 50A was set to be the same. Further, as the burners 3 1A to 50A of Example 11, only an oxygen burner was used, and as the burners 31A to 50A of Example 12, an oxygen burner and an air burner were used. [Table 3] Example 11 Example 12 Oxygen burner fuel Natural gas Natural gas air burner No. - 39A, 49A Air burner fuel - Natural gas total combustion heat per hour Qa (kWh) 10000 12200 Oxygen burner relative to Contribution rate of Qa (%) 100 74 Total heating amount per hour Qb (kWh) 7300 7300 Contribution rate of oxygen burner to Qb (%) 100 90 CO2 emission per hour (Nm3/h) 1050 1250 Distance between the L(m) 12 12 exhaust port and the air burner farthest from the exhaust port in the front-rear direction La(m) - 8 La/L - 0.67 Air burner per 1 specific area Contribution rate (%) of total combustion heat Qd in hours - 51 P-OH (mm'') 0.51 0.45 As understood from Table 3, in Example 12, from the exhaust ports 24A, 25A toward the rear 155915.doc -25 - 201141803 In the area where the distance is 0.6L or more, each of the air burners and the oxygen burner is provided. Compared with the case of Example 11, the p_〇H in the glass is decreased by more than 1%. From this, it was judged that in Example 12, the amount of moisture dissolved in the glazing glass in the melting chamber 1 可 was sufficiently adjusted by adjusting the ratio of the combustion heat per hour of the air burner to the oxy-combustion burner. (Examples 13 to 14) In Examples 13 to 14 (Table 4), β_0Η (unit: /mm) in the glass produced by using the glass melting furnace shown in Figs. 6 and 7 was obtained by the above calculation. Example 14 is an example, and Example 13 is a comparative example. In each of Examples 13 to 14, the melting direction of the melting chamber 10B was set to 3 m, the width direction γ3 of the melting chamber 10B was set to 2 m, and the height direction dimension 23 of the melting chamber 10B was set to 2 me. , set the volume of the molten glass in the melting chamber i〇b to 4.5 m3, which will be! The volume of the glass raw material (i.e., the smelting glass taken out from the refining chamber) which is melted into 10B is set to 〇〇4 m3 〇 and then the exhaust port 24b, 25B is set to the front and rear direction size X4. 〇.3 m, the height direction dimension Z4 of the exhaust ports 24B, 25B is set to 0 3 m. Further, in the left side wall nB, the distance l5 in the front-rear direction between the front wall 1 and the exhaust port 24B is set to 〇.2 m 'the distance between the exhaust port 24B and the burner 31B in the front-rear direction. Let 疋.3 m ' set the distance in the front-rear direction between the exhaust port 24B and the burner 32B to 10 m, and set the distance in the front-rear direction between the exhaust port 24B and the burner 33B to 2 〇m. On the other hand, in the right side wall 1, the distance L5 in the front-rear direction between the front wall 11B and the exhaust port 25B is set to 〇·2 m 'the front and rear direction between the exhaust port 25B and the burner 41B, respectively. 155915.doc
S •26· 201141803 上之距離設定為0.5 m,將排氣口 25B與燃燒器42B之間的 前後方向上之距離設定為1.5 m。並且,於各例13~14中, 將複數個燃燒器31B〜33B、41B〜42B各自之每1小時之燃燒 熱量設定為相同。再者,作為例13之燃燒器31B〜33B、 41B〜42B,係僅使用氧燃燒器,作為例14之燃燒器 31B〜33B、41B〜42B,係使用氧燃燒器與空氣燃燒器。 [表4] 例13 例14 氧燃燒器之燃料 天然氣 天然氣 空氣燃燒器之No. - 42B 空氣燃燒器之燃料 - 天然氣 每1小時之總燃燒熱量Qa(kWh) 500 720 氧燃燒器相對於Qa之貢獻率(%) 100 56 每1小時之總加熱量Qb(kWh) 370 370 氧燃燒器相對於Qb之貢獻率(%) 100 80 每1小時之C02排出量(Nm3/h) 50 75 距離L(m) 2.5 排氣口與離排氣口最遠的空氣燃燒器之間的前後方向上之距離La(m) - 1.5 La/L - 0.6 空氣燃燒器相對於特定區域之每1小時之總燃燒熱量Qd的貢獻率(%) - 76 p-OH(mm·】) 0.52 0.46 如根據表4所理解,例14中,於自排氣口 24B、25B朝後 方離開0.6L以上之區域中,各設置有至少1個空氣燃燒器 及氧燃燒器,與例13之情形相比,玻璃板中之β-ΟΗ下降 10%以上。由此而判定,例14中,藉由調節空氣燃燒器與 氧燃燒器每1小時之燃燒熱量比而可充分調節熔解室10 Β内 之熔融玻璃中溶存之水分量。 以上參照特定之實施態樣對本發明進行了詳細說明,但 155915.doc -27- 201141803 本領域技術人貝明確暸解,可*麟本發明之精神與範圍 而進行各種變更或修正。 本申請係基於2010年4月26曰申請之曰本專利申請案 2010-101312者’其内容作為參照而被引入於此。 產業上之可利用性 根據本發明,可提供一種可抑制NOx排出量之增加、且 可充分調節熔融玻璃中溶存之水分量的玻璃熔解爐。該玻 璃熔解爐於對熔融玻璃進行充分加熱並使水分量降低之情 形時特別有效。 【圖式簡單說明】 圖1係本發明之實施形態之玻璃製品之製造方法之步驟 圖。 圖2係第1實施形態之玻璃熔解爐之内部結構之側視圖。 圖3係第1實施形態之玻璃熔解爐之内部結構之俯視圖。 圖4係第2實施形態之玻璃熔解爐之内部結構之側視圖。 圖5係第2實施形態之玻璃熔解爐之内部結構之俯視圖。 圖6係第3實施形態之玻璃炫解爐之内部結構之側視圖。 圖7係第3實施形態之玻璃熔解爐之内部結構之俯視圖。 圖8係玻璃熔解爐之内部結構之變形例之俯視圖。 圖9係玻璃熔解爐之内部結構之其他變形例之俯視圖。 【主要元件符號說明】 1、1A、IB、1D 熔解爐 10、10B、l〇C、10D 熔解室 11、11B、11C、11D 前壁 155915.docThe distance on S • 26· 201141803 is set to 0.5 m, and the distance between the exhaust port 25B and the burner 42B in the front-rear direction is set to 1.5 m. Further, in each of Examples 13 to 14, the heat of combustion per one hour of each of the plurality of burners 31B to 33B and 41B to 42B was set to be the same. Further, as the burners 31B to 33B and 41B to 42B of the example 13, only the oxygen burner was used, and as the burners 31B to 33B and 41B to 42B of the example 14, the oxygen burner and the air burner were used. [Table 4] Example 13 Example 14 Fuel of Oxygen Burner Natural Gas Air Burner No. - 42B Fuel of Air Burner - Total Combustion Heat per Natural Gas Qa (kWh) 500 720 Oxygen Burner Relative to Qa Contribution rate (%) 100 56 Total heating amount per hour Qb (kWh) 370 370 Contribution rate of oxygen burner to Qb (%) 100 80 C02 emission per hour (Nm3/h) 50 75 Distance L (m) 2.5 Distance between the exhaust port and the air burner farthest from the exhaust port in the front-rear direction La(m) - 1.5 La/L - 0.6 Total of the air burner per hour for a specific area The contribution rate (%) of the heat of combustion Qd - 76 p - OH (mm · )) 0.52 0.46 As understood from Table 4, in the example 14, in the region which is separated from the exhaust ports 24B, 25B by 0.6 L or more, Each of the air burners and the oxygen burners was provided, and the β-ΟΗ in the glass plate was reduced by 10% or more as compared with the case of Example 13. From this, it was judged that in Example 14, the amount of moisture dissolved in the molten glass in the melting chamber 10 was sufficiently adjusted by adjusting the ratio of the combustion heat per hour of the air burner to the oxygen burner. The present invention has been described in detail above with reference to the specific embodiments thereof. However, it is to be understood that those skilled in the art can make various changes or modifications in the spirit and scope of the invention. The present application is based on a patent application No. 2010-101312 filed on Apr. 26, 2010, the content of which is hereby incorporated by reference. Industrial Applicability According to the present invention, it is possible to provide a glass melting furnace capable of suppressing an increase in the amount of NOx discharged and sufficiently adjusting the amount of water dissolved in the molten glass. This glass melting furnace is particularly effective in the case where the molten glass is sufficiently heated and the moisture content is lowered. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a view showing the steps of a method for producing a glass product according to an embodiment of the present invention. Fig. 2 is a side view showing the internal structure of the glass melting furnace of the first embodiment. Fig. 3 is a plan view showing the internal structure of the glass melting furnace of the first embodiment. Fig. 4 is a side view showing the internal structure of a glass melting furnace according to a second embodiment. Fig. 5 is a plan view showing the internal structure of a glass melting furnace according to a second embodiment. Fig. 6 is a side view showing the internal structure of the glass decontamination furnace of the third embodiment. Fig. 7 is a plan view showing the internal structure of a glass melting furnace according to a third embodiment. Fig. 8 is a plan view showing a modification of the internal structure of the glass melting furnace. Fig. 9 is a plan view showing another modification of the internal structure of the glass melting furnace. [Main component symbol description] 1, 1A, IB, 1D melting furnace 10, 10B, l〇C, 10D melting chamber 11, 11B, 11C, 11D front wall 155915.doc
S 201141803 12、12B、12D 後壁 13、13B、13C、13D 側壁(左側壁) 14、14B、14C、14D 側壁(右側壁) 15 熔解槽 16 頂棚 17 ' 18 室 19 縮頸部 21 、 21B 、 21D 原料投入口 22 、 22B 取出口 23 、 23B 流路 24、24B、24C、25、25B、25C 排氣口 31 〜50、31B-33B、41B〜42B 燃燒器 G1 玻璃原料 G2 熔融玻璃 L、LI、L2、L3、L4、L5、L6 距離 XI、X2、X3、X4 前後方向尺寸 Yl、Y3 寬度方向尺寸 Zl 、 Z2 、 Z3 、 Z4 南度方向尺寸 155915.doc -29-S 201141803 12, 12B, 12D Rear wall 13, 13B, 13C, 13D Side wall (left side wall) 14, 14B, 14C, 14D Side wall (right side wall) 15 Melting tank 16 Ceiling 17 ' 18 Chamber 19 Constricted neck 21, 21B, 21D raw material input port 22, 22B take-out port 23, 23B flow path 24, 24B, 24C, 25, 25B, 25C exhaust port 31 to 50, 31B-33B, 41B to 42B burner G1 glass material G2 molten glass L, LI , L2, L3, L4, L5, L6 Distance XI, X2, X3, X4 Front and back direction dimension Yl, Y3 Width direction dimension Zl, Z2, Z3, Z4 South dimension size 155915.doc -29-
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| JP6292090B2 (en) * | 2014-09-03 | 2018-03-14 | 旭硝子株式会社 | Melting kiln, melting method, and alkali-free glass plate manufacturing method |
| US10759688B2 (en) * | 2015-06-26 | 2020-09-01 | Owens Corning Intellectual Capital, Llc | Glass melter with oxygen/gas heat-up burner system |
| JP6749123B2 (en) * | 2016-03-31 | 2020-09-02 | AvanStrate株式会社 | Glass substrate manufacturing method and glass substrate manufacturing apparatus |
| JP6631372B2 (en) * | 2016-04-08 | 2020-01-15 | Agc株式会社 | Melting method and method for producing alkali-free glass plate |
| JP7760930B2 (en) | 2022-02-21 | 2025-10-28 | Agc株式会社 | Glass melting furnace, glass product manufacturing equipment, and glass product manufacturing method |
| JP7722217B2 (en) * | 2022-02-21 | 2025-08-13 | Agc株式会社 | Glass melting furnace, glass product manufacturing equipment, and glass product manufacturing method |
| EP4509472A4 (en) | 2022-04-15 | 2025-07-16 | Nippon Electric Glass Co | METHOD FOR MANUFACTURING A GLASS ARTICLE |
| US20250223214A1 (en) | 2022-04-15 | 2025-07-10 | Nippon Electric Glass Co., Ltd. | Method for producing glass article |
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| US6519973B1 (en) * | 2000-03-23 | 2003-02-18 | Air Products And Chemicals, Inc. | Glass melting process and furnace therefor with oxy-fuel combustion over melting zone and air-fuel combustion over fining zone |
| DE10055924B4 (en) * | 2000-08-19 | 2006-03-23 | Horn Glasanlagen Gmbh | Method for operating a glass melting furnace |
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