本發明之光學玻璃以氧化物換算組成之質量%計,含有20.0~60.0%之SiO2
成分、10.0~50.0%之Nb2
O5
成分,部分分散比(θg,F)於與阿貝數(νd
)之間滿足(-0.00256×νd
+0.637)≦(θg,F)≦(-0.00256×νd
+0.684)之關係。 於含有SiO2
成分及Nb2
O5
成分之玻璃中,能獲得具有所需範圍內之高折射率或低阿貝數(高分散)及低部分分散比之玻璃。 因此,能夠獲得具有所需之高折射率(nd
)及低阿貝數(νd
)並且部分分散比(θg,F)較小而對光學系統之色像差降低有用之光學玻璃。 特別是,第1光學玻璃以氧化物換算組成之質量%計,含有20.0~60.0%之SiO2
成分、20.0~45.0%之Nb2
O5
成分、1.0~20.0%之ZrO2
成分,具有1.60以上1.75以下之折射率(nd
)及30以上47以下之阿貝數(νd
),部分分散比(θg,F)於與阿貝數(νd
)之間滿足(-0.00256×νd
+0.637)≦(θg,F)≦(-0.00256×νd
+0.684)之關係。 第1光學玻璃中,於含有SiO2
成分、Nb2
O5
成分及ZrO2
成分之玻璃中,能獲得具有所需範圍內之高折射率或低阿貝數(高分散)及低部分分散比之玻璃。 因此,能夠獲得具有所需之高折射率(nd
)及低阿貝數(νd
)並且部分分散比(θg,F)較小而對光學系統之色像差降低有用之光學玻璃。 又,第2光學玻璃以氧化物換算組成之質量%計,含有20.0~60.0%之SiO2
成分、10.0~50.0%之Nb2
O5
成分、超過0.1且至15.0%之K2
O成分,部分分散比(θg,F)於與阿貝數(νd
)之間滿足(-0.00256×νd
+0.637)≦(θg,F)≦(-0.00256×νd
+0.684)之關係,表面法耐候性為級1或2。 第2光學玻璃中,於含有SiO2
成分、Nb2
O5
成分及K2
O成分之玻璃中,能夠獲得具有所需範圍內之高折射率或低阿貝數(高分散)及低部分分散比之玻璃,特別是藉由含有K2
O成分,所需之光學常數之調整變得容易,能夠在保持使部分分散比(θg,F)較小之狀態下,減少變色之產生。 因此,能夠獲得如下之光學玻璃,其具有所需之高折射率(nd
)及低阿貝數(νd
),並且部分分散比(θg,F)較小,對光學系統之色像差降低有用,且化學耐久性、特別是表面法耐候性良好。 以下,對本發明之光學玻璃之實施形態進行詳細說明,本發明並不受以下之實施形態任何限定,能夠於本發明之目的之範圍內,適當添加變更而實施。再者,對於說明重複之部分,存在適當省略說明之情形,但並不限定發明之主旨。 [玻璃成分] 以下對於構成本發明之光學玻璃之各成分之組成範圍進行敍述。本說明書中無特別說明之情形時,各成分之含量係由相對於所有氧化物換算組成之玻璃總質量之質量%所表示。此處,所謂「氧化物換算組成」係於假設作為本發明之玻璃構成成分之原料而使用之氧化物、複合鹽、金屬氟化物等在熔融時全部分解變成氧化物之情形時,將該生成氧化物之總質量設為100質量%,標明玻璃中所含有之各成分之組成。 <關於必須成分、任意成分> SiO2
成分係因能夠促進穩定之玻璃形成且降低液相溫度而減少作為光學玻璃而言不佳之失透(結晶物之產生)之必須成分。 特別是,藉由使SiO2
成分之含量為20.0%以上,不會大幅度提高部分分散比,而能夠獲得耐失透性優異之玻璃。又,藉此能夠減少於玻璃形成時或再加熱時等之失透或著色。因此,SiO2
成分之含量係將較佳為20.0%、更佳為23.0%、進而較佳為25.0%、進而較佳為27.0%、進而較佳為30.0%、進而較佳為32.0%作為下限。 另一方面,藉由使SiO2
成分之含量為60.0%以下而使折射率不易降低,以此能夠容易獲得所需之高折射率,並且,能抑制部分分散比之上升。又,藉此能抑制玻璃原料之熔解性之降低。因此,SiO2
成分之含量係將較佳為60.0%、更佳為55.0%、進而較佳為50.0%、進而較佳為48.0%、進而較佳為47.0%、進而較佳為45.0%、進而較佳為44.0%、進而較佳為43.0%作為上限。 SiO2
成分能夠使用SiO2
、K2
SiF6
、Na2
SiF6
等作為原料。 Nb2
O5
成分係能夠提高折射率且降低阿貝數及部分分散比、並且能提高耐失透性之必須成分。 特別是,藉由使Nb2
O5
成分之含量為10.0%以上,可提高折射率且於本發明之範圍之成分內調整至目標光學常數,以此能夠減小異常分散性。因此,Nb2
O5
成分之含量係將較佳為10.0%,更佳為15.0%,進而較佳為20.0%,更佳為22.0%,進而較佳為23.0%作為下限。 另一方面,藉由使Nb2
O5
成分之含量為50.0%以下,能夠降低玻璃之材料成本。又,能夠抑制玻璃製造時之熔解溫度之上升,並且減少因Nb2
O5
成分之過剩含有所導致之失透。進而,亦能夠使玻璃之化學耐久性惡化改善。因此,Nb2
O5
成分之含量係將較佳為50.0%、更佳為45.0%、進而較佳為43.0%、進而較佳為41.5%、進而較佳為40.0%、進而較佳為35.0%、進而較佳為30.0%作為上限。 Nb2
O5
成分能夠使用Nb2
O5
等作為原料。 ZrO2
成分係於含有超過0%之情形時能夠提高玻璃之折射率及阿貝數、降低部分分散比並且提高耐失透性之成分,特別是於第1光學玻璃中為必須成分。又,藉由含有ZrO2
成分,能夠減少於玻璃形成時或再加熱時等之失透或著色。因此,ZrO2
成分之含量亦可較佳為1.0%以上,更佳為超過1.0%,進而較佳為超過3.0%,進而較佳為超過5.0%。 另一方面,藉由使ZrO2
成分之含量為20.0%以下,能夠減少失透,並且能夠容易獲得更均質之玻璃。因此,ZrO2
成分之含量係將較佳為20.0%、更佳為18.0%、進而較佳為15.0%、進而較佳為13.0%、進而較佳為10.0%作為上限。 ZrO2
成分能夠使用ZrO2
、ZrF4
等作為原料。 K2
O成分係於含有超過0%之情形時能提高玻璃原料之熔解性並且能夠降低液相溫度之任意成分。特別是於第2光學玻璃中,K2
O成分為能夠使化學耐久性改善之必須成分。 特別是,藉由含有K2
O成分之含量超過0%,能夠有效改善玻璃中之變色。因此,K2
O成分之含量亦可較佳為超過0%,更佳為超過0.1%,進而較佳為超過0.3%,進而較佳為超過0.5%,進而較佳為超過1.0%。 另一方面,藉由使K2
O成分之含量為15.0%以下,能抑制部分分散比之上升,能夠減少失透,並且能夠使化學耐久性不易惡化。因此,K2
O成分之含量較佳為15.0%以下,更佳為10.0%以下,進而較佳為未達10.0%,進而較佳為未達8.0%,進而較佳為未達5.0%。 K2
O成分能夠使用K2
CO3
、KNO3
、KF、KHF2
、K2
SiF6
等作為原料。 ZnO成分係於含有超過0%之情形時廉價且能夠提高耐失透性、並且能降低玻璃轉移點之任意成分。因此,ZnO成分之含量亦可較佳為超過0%,更佳為超過0.5%,進而較佳為超過1.0%。 另一方面,藉由使ZnO成分之含量為25.0%以下,減少於玻璃形成時或再加熱時等之失透或著色,並且能提高化學耐久性。因此,ZnO成分之含量較佳為25.0%以下,更佳為20.0%以下,進而較佳為未達18.0%,進而較佳為未達14.0%,進而較佳為未達13.0%,進而較佳為未達10.0%。 Li2
O成分係於含有超過0%之情形時能夠降低部分分散比、改善透過率、降低液相溫度、並且能提高玻璃原料之熔解性之任意成分。因此,Li2
O成分之含量亦可較佳為超過0%,更佳為超過1.0%,進而較佳為超過3.0%,進而較佳為超過5.0%。 另一方面,藉由使Li2
O成分之含量為20.0%以下,能抑制折射率之降低,能夠使化學耐久性不易惡化,並且能夠減少因過剩含有所導致之失透。 因此,Li2
O成分之含量較佳為20.0%以下,更佳為15.0%以下,進而較佳為13.0%以下,進而較佳為未達10.0%,進而較佳為未達8.0%。 Li2
O成分能夠使用Li2
CO3
、LiNO3
、LiF等作為原料。 Na2
O成分係於含有超過0%之情形時能夠降低部分分散比、能夠降低液相溫度、並且能提高玻璃原料之熔解性之任意成分。因此,Na2
O成分之含量亦可較佳為超過0%,更佳為超過1.0%,進而較佳為超過3.0%,進而較佳為超過5.0%。 另一方面,藉由使Na2
O成分之含量為20.0%以下,能抑制折射率之降低,能夠使化學耐久性不易惡化,並且能夠減少因過剩含有所導致之失透。 因此,Na2
O成分之含量較佳為20.0%以下,更佳為15.0%以下,進而較佳為13.0%以下,進而較佳為未達10.0%,進而較佳為未達8.0%。 Na2
O成分能夠使用Na2
CO3
、NaNO3
、NaF、Na2
SiF6
等作為原料。 B2
O3
成分係如下之任意成分:於含有超過0%之情形時,能夠促進穩定之玻璃形成,又,能夠降低液相溫度,因此能提高耐失透性,並且能提高玻璃原料之熔解性。因此,B2
O3
成分之含量亦可較佳為超過0%,更佳為超過0.1%,進而較佳為超過1.0%,進而較佳為超過3.0%,進而較佳為超過5.0%。特別是,就於低溫成形熔融玻璃使耐失透性提高及脈理減少之觀點而言,較理想為含有3.0%以上之B2
O3
成分,亦可更佳為5.0%以上,進而較佳為7.0%以上。 另一方面,藉由使B2
O3
成分之含量為20.0%以下,能抑制折射率之降低,並且能抑制部分分散比之上升。進而亦能夠改善玻璃之化學耐久性惡化。因此,B2
O3
成分之含量係將較佳為20.0%、更佳為18.0%、進而較佳為15.0%、進而較佳為12.0%作為上限。 B2
O3
成分能夠使用H3
BO3
、Na2
B4
O7
、Na2
B4
O7
・10H2
O、BPO4
等作為原料。 TiO2
成分係於含有超過0%之情形時提高折射率、降低阿貝數、並且提高耐失透性之任意成分。 另一方面,藉由使TiO2
成分之含量為15.0%以下,能夠減少玻璃之著色,而能提高內部透過率。又,藉此,部分分散比不易上升,故能夠容易獲得接近正規線之所需之低部分分散比。因此,TiO2
成分之含量較佳為15.0%以下,更佳為10.0%以下,進而較佳為5.0%以下,進而較佳為未達5.0%,進而較佳為未達3.0%,進而較佳為2.0%以下,進而較佳為未達1.0%。特別是,就減小玻璃之異常分散性之觀點而言,較理想為實質上不包含。 TiO2
成分能夠使用TiO2
等作為原料。 MgO成分係於含有超過0%之情形時能夠降低玻璃之熔解溫度之任意成分。 另一方面,藉由使MgO成分之含量為10.0%以下,能夠抑制折射率之降低,並且減少失透。因此,MgO成分之含量較佳為10.0%以下,更佳為未達5.0%,進而較佳為未達3.0%,進而較佳為未達1.0%。 MgO成分能夠使用MgO、MgCO3
、MgF2
等作為原料。 CaO成分係於含有超過0%之情形時能夠降低玻璃之材料成本、降低阿貝數、能夠減少失透、並且能提高玻璃原料之熔解性之任意成分。因此,CaO成分之含量亦可較佳為超過0%,更佳為超過1.0%,進而較佳為超過2.0%。 另一方面,藉由使CaO成分之含量為10.0%以下,能抑制折射率之降低或阿貝數之上升、部分分散比之上升,並且能夠降低失透。因此,CaO成分之含量較佳為10.0%以下,更佳為未達5.0%,進而較佳為未達3.0%,進而較佳為未達1.0%。 CaO成分能夠使用CaCO3
、CaF2
等作為原料。 SrO成分係於含有超過0%之情形時能提高折射率並且能提高耐失透性之任意成分。 特別是,藉由使SrO成分之含量為10.0%以下,能抑制化學耐久性之惡化。因此,SrO成分之含量較佳為10.0%以下,更佳為未達5.0%,進而較佳為3.0%以下,進而較佳為未達3.0%,進而較佳為未達1.0%。 SrO成分能夠使用Sr(NO3
)2
、SrF2
等作為原料。 BaO成分係如下之任意成分:於含有超過0%之情形時,能提高折射率,能夠降低部分分散比,能提高耐失透性,能提高玻璃原料之熔解性,並且與其他鹼土成分相比,能夠降低玻璃之材料成本。 特別是,藉由使BaO成分之含量為10.0%以下,能抑制折射率之降低或阿貝數之上升、部分分散比之上升,並且能夠減少失透。因此,BaO成分之含量較佳為10.0%以下,更佳為未達5.0%,進而較佳為未達3.0%,進而較佳為未達1.0%。 BaO成分能夠使用BaCO3
、Ba(NO3
)2
等作為原料。 La2
O3
成分、Gd2
O3
成分、Y2
O3
成分及Yb2
O3
成分係藉由含有至少任一種超過0%而能夠提高折射率並且減小部分分散比之任意成分。 特別是,藉由使La2
O3
成分、Gd2
O3
成分、Y2
O3
成分及Yb2
O3
成分各自之含量為10.0%以下,能抑制阿貝數之上升,能夠減少失透,並且能夠降低材料成本。因此,La2
O3
成分、Gd2
O3
成分、Y2
O3
成分及Yb2
O3
成分各自之含量係將較佳為10.0%、更佳為5.0%、進而較佳為3.0%作為上限,進而較佳為未達1.0%。 La2
O3
成分、Gd2
O3
成分、Y2
O3
成分及Yb2
O3
成分能夠使用La2
O3
、La(NO3
)3
・XH2
O(X為任意整數)、Y2
O3
、YF3
、Gd2
O3
、GdF3
、Yb2
O3
等作為原料。 Ta2
O5
成分係於含有超過0%之情形時為提高折射率降低阿貝數及部分分散比並且能提高耐失透性之任意成分。 另一方面,藉由使Ta2
O5
成分之含量為10.0%以下,作為稀有礦物資源之Ta2
O5
成分之使用量減少,並且玻璃變得更容易於低溫熔解,故能夠降低玻璃之生產成本。又,藉此能夠減少因Ta2
O5
成分之過剩含有所導致之玻璃之失透。因此,Ta2
O5
成分之含量較佳為10.0%以下,更佳為未達5.0%,進而較佳為未達3.0%,進而較佳為未達1.0%。特別是就降低玻璃之材料成本之觀點而言,亦可不含有Ta2
O5
成分。 Ta2
O5
成分能夠使用Ta2
O5
等作為原料。 WO3
成分係於含有超過0%之情形時提高折射率降低阿貝數、提高耐失透性、並且能提高玻璃原料之熔解性之任意成分。 另一方面,藉由使WO3
成分之含量為10.0%以下,能夠使玻璃之部分分散比不易上升,並且能減少玻璃之著色而提高內部透過率。因此,WO3
成分之含量較佳為10.0%以下,更佳為未達5.0%,進而較佳為未達3.0%,進而較佳為未達1.0%。 WO3
成分能夠使用WO3
等作為原料。 P2
O5
成分係於含有超過0%之情形時能提高玻璃之穩定性之任意成分。 另一方面,藉由使P2
O5
成分之含量為10.0%以下,能夠減少因P2
O5
成分之過剩含有所導致之失透。因此,P2
O5
成分之含量較佳為10.0%以下,更佳為未達5.0%,進而較佳為未達3.0%,進而較佳為未達1.0%。 P2
O5
成分能夠使用Al(PO3
)3
、Ca(PO3
)2
、Ba(PO3
)2
、BPO4
、H3
PO4
等作為原料。 GeO2
成分係於含有超過0%之情形時提高折射率並且能夠減少失透之任意成分。 另一方面,藉由使GeO2
成分之含量為10.0%以下,而使高價之GeO2
成分之使用量得以減少,因此能夠降低玻璃之材料成本。因此,GeO2
成分之含量較佳為10.0%以下,更佳為未達5.0%,進而較佳為未達3.0%,進而較佳為未達1.0%。 GeO2
成分能夠使用GeO2
等作為原料。 Al2
O3
成分及Ga2
O3
成分係於含有至少任一種超過0%之情形時能夠提高化學耐久性並且提高耐失透性之任意成分。 另一方面,藉由使Al2
O3
成分及Ga2
O3
成分各自之含量為10.0%以下,能夠減少因Al2
O3
成分或Ga2
O3
成分之過剩含有所導致之失透。因此,Al2
O3
成分及Ga2
O3
成分各自之含量較佳為10.0%以下,更佳為未達5.0%,進而較佳為未達3.0%,進而較佳為未達1.0%。 Al2
O3
成分及Ga2
O3
成分能夠使用Al2
O3
、Al(OH)3
、AlF3
、Ga2
O3
、Ga(OH)3
等作為原料。 Bi2
O3
成分係於含有超過0%之情形時能夠提高折射率、降低阿貝數、並且能夠降低玻璃轉移點之任意成分。 另一方面,藉由使Bi2
O3
成分之含量為10.0%以下,能夠使部分分散比不易上升,並且能夠減少玻璃之著色而提高內部透過率。因此,Bi2
O3
成分之含量較佳為10.0%以下,更佳為未達5.0%,進而較佳為未達3.0%,進而較佳為未達1.0%。 Bi2
O3
成分能夠使用Bi2
O3
等作為原料。 TeO2
成分係於含有超過0%之情形時能夠提高折射率、降低部分分散比、並且能夠降低玻璃轉移點之任意成分。 另一方面,藉由使TeO2
成分之含量為5.0%以下,能夠減少玻璃之著色而提高內部透過率。又,藉由減少高價之TeO2
成分之使用,能獲得材料成本更便宜之玻璃。因此,TeO2
成分之含量較佳為5.0%以下,進而較佳為未達3.0%,進而較佳為未達1.0%。 TeO2
成分能夠使用TeO2
等作為原料。 SnO2
成分係於含有超過0%之情形時能夠使熔解之玻璃澄清(消泡)並且能提高玻璃之可見光透過率之任意成分。 另一方面,藉由使SnO2
成分之含量為1.0%以下,能夠使因熔融玻璃之還原所導致之玻璃之著色或玻璃之失透不易產生。又,由於減少了SnO2
成分與熔解設備(特別是Pt等貴金屬)之合金化,故而能夠謀求熔解設備之長壽命化。因此,SnO2
成分之含量較佳為1.0%以下,更佳為未達0.5%,進而較佳為未達0.1%。 SnO2
成分能夠使用SnO、SnO2
、SnF2
、SnF4
等作為原料。 Sb2
O3
成分係於含有超過0%之情形時促進玻璃之消泡並使玻璃澄清之成分,且為本發明之光學玻璃中之任意成分。Sb2
O3
成分藉由使相對於玻璃總質量之含量為1.0%以下,能夠不易產生玻璃熔融時之過度發泡,能夠使Sb2
O3
成分不易與熔解設備(特別是Pt等貴金屬)合金化。因此,相對於氧化物換算組成之玻璃總質量之Sb2
O3
成分之含有率係將較佳為1.0%、更佳為0.8%、進而較佳為0.6%作為上限。此處,特別是就容易獲得曝曬作用較低之光學玻璃之觀點而言,氧化物換算組成之玻璃總質量Sb2
O3
成分之含量係將較佳為0.5%、更佳為0.3%、進而較佳為0.1%作為上限。 再者,使玻璃澄清並消泡之成分並不限定於上述Sb2
O3
成分,能夠使用玻璃製造領域中之公知之澄清劑或消泡劑、或者其等之組合。 相對於ZrO2
成分及Li2
O成分之含量之和而言的Li2
O成分及K2
O成分之含量之和之比率較佳為超過0且未達2.5。 特別是,藉由將該質量比設為超過0,能夠使失透性及透過率改善。因此,(Li2
O+K2
O)/(ZrO2
+Li2
O)之下限值能夠較佳為超過0,更佳為超過0.1,進而較佳為超過0.3。 另一方面,藉由將該質量比設為未達2.5,能夠於保持玻璃之折射率之狀態下,減小玻璃之異常分散性。因此,(Li2
O+K2
O)/(ZrO2
+Li2
O)之上限值亦可較佳為未達2.5,更佳為2.1以下,進而較佳為未達2.0,進而較佳為未達1.5,進而較佳為未達1.0,進而較佳為未達0.5。 SiO2
成分及Nb2
O5
成分之合計(質量和)較佳為超過50.0%。藉此,能夠獲得化學耐久性優異並且異常分散較小、保持有某種固定程度之黏性且成形性良好之玻璃。 因此,該質量和亦可較佳為超過50.0%,更佳為53.0%以上,進而較佳為54.0%以上,進而較佳為58.0%以上。 另一方面,該質量和亦可較佳為90.0%以下,更佳為未達85.0%,進而較佳為未達81.0%,進而較佳為未達76.0%。 Ln2
O3
成分(式中,Ln係選自由La、Gd、Y、Yb所組成之群中之1種以上)之含量之和(質量和)較佳為15.0%以下。藉此,能夠減少玻璃之失透,能抑制阿貝數之上升,並且能夠降低玻璃之材料成本。因此,Ln2
O3
成分之質量和較佳為15.0%以下,更佳為未達10.0%,進而較佳為未達5.0%,進而較佳為未達3.5%。 藉由使Rn2
O成分(式中,Rn係選自由Li、Na、K所組成之群中之1種以上)之含量之和(質量和)為超過0%,能夠提高玻璃原料之熔解性,並且降低玻璃轉移點。因此,Rn2
O成分之含量亦可較佳為超過0%,更佳為5.0%以上,進而較佳為超過5.0%,進而較佳為8.0%以上,進而較佳為10.0%以上,進而較佳為超過10.0%,進而較佳為12.0%以上,進而較佳為超過13.0%。 另一方面,Rn2
O成分(式中,Rn係選自由Li、Na、K所組成之群中之1種以上)之含量之和(質量和)較佳為30.0%以下。藉此,能夠使玻璃之折射率不易降低,減少玻璃形成時之失透。又,能夠加固玻璃中之黏性,改善成形性。因此,Rn2
O成分之合計含量係將較佳為30.0%、更佳為25.0%、進而較佳為20.0%、進而較佳為17.0%作為上限。 RO成分(式中,R係選自由Mg、Ca、Sr、Ba所組成之群中之1種以上)之含量之和(質量和)較佳為30.0%以下。藉此,能夠減少因該等成分之過剩含有所導致之玻璃之失透。因此,RO成分之質量和較佳為30.0%以下,更佳為25.0%以下,進而較佳為20.0%以下,進而較佳為15.0%以下,進而較佳為未達10.0%,進而較佳為未達5.0%。 另一方面,RO成分之質量和就提高玻璃原料之熔解性並且減少失透之觀點而言,亦可較佳為超過0%,更佳為1.0%以上,進而較佳為2.0%以上。 <關於不應含有之成分> 繼而,對本發明之光學玻璃中不應含有之成分及含有則不佳之成分進行說明。 能夠於不損及本案發明之玻璃之特性之範圍內視需要添加其他成分。但是,除了Ti、Zr、Nb、W、La、Gd、Y、Yb、Lu以外,V、Cr、Mn、Fe、Co、Ni、Cu、Ag及Mo等各過渡金屬成分具有即便單獨或複合地含有少量之各者之情形時亦會使玻璃著色而對可見區域可見區域之特定波長產生吸收的性質,因此特別是於使用可見光區域之波長之光學玻璃中,較佳為實質上不包含。 又,PbO等鉛化合物及As2
O3
等砷化合物由於為環境負荷較高之成分,故而較理想為實質上不包含,即除了不可避免之混入以外,一概不含有。 進而,Th、Cd、Tl、Os、Be、及Se之各成分近年來有作為有害化學物資而控制其使用之傾向,不僅玻璃之製造步驟,直至加工步驟、及製品化後之處理,均需要環境對策上之措施。因此,於重視環境上之影響之情形時,較佳為實質上不含有該等。 [製造方法] 本發明之光學玻璃例如以如下方式製作。即,藉由如下步驟而製作:將上述原料以各成分處於特定之含量之範圍內之方式均勻混合,將所製作之混合物投入鉑坩堝、石英坩堝或氧化鋁坩堝進行粗熔融之後,放入金坩堝、鉑坩堝、鉑合金坩堝或銥坩堝中於1000~1400℃之溫度範圍熔融3~5小時,予以攪拌均質化而進行消泡等之後,降溫至900~1100℃之溫度後進行精攪拌以去除脈理,澆鑄入模具中並進行緩冷。 <物性> 本發明之光學玻璃具有高折射率及特定範圍之阿貝數。 本發明之光學玻璃之折射率(nd
)係將較佳為1.60、更佳為1.63、進而較佳為1.65作為下限。該折射率之上限較佳為1.78,更佳為1.77,進而較佳為1.76,進而較佳為1.75,進而較佳為1.73,進而較佳為1.70。 本發明之光學玻璃之阿貝數(νd
)係將較佳為28、更佳為29、進而較佳為30、進而較佳為31、進而較佳為33作為下限。另一方面,本發明之光學玻璃之阿貝數(νd
)係將較佳為47、更佳為45、進而較佳為43、進而較佳為42、進而較佳為41、進而較佳為40作為上限。 具有此種折射率及阿貝數之本發明之光學玻璃於光學設計上有用,特別是能夠謀求高成像特性等,且亦能夠謀求光學系統之小型化,故能夠擴展光學設計之自由度。 本發明之光學玻璃具有低部分分散比(θg,F)。 更具體而言,本發明之光學玻璃之部分分散比(θg,F),又,本發明之光學玻璃之部分分散比(θg,F)較佳為於與阿貝數(νd
)之間滿足 (-0.00256×νd
+0.637)≦(θg,F)≦(-0.00256×νd
+0.684)之關係。 因此,本發明之光學玻璃中,部分分散比(θg,F)與阿貝數(νd
)較佳為滿足θg,F≧(-0.00256×νd
+0.637)之關係,更佳為滿足θg,F≧ (-0.00256×νd
+0.647)之關係,進而較佳為滿足θg,F≧(-0.00256×νd
+0.657)之關係。 另一方面,本發明之光學玻璃中,部分分散比(θg,F)與阿貝數(νd
)較佳為滿足θg,F≦(-0.00256×νd
+0.684)之關係,更佳為滿足θg,F≦ (-0.00256×νd
+0.681)之關係,進而較佳為滿足θg,F≦(-0.00256×νd
+0.677)之關係。 藉此,能獲得具有低部分分散比(θg,F)之光學玻璃,故自該光學玻璃所形成之光學元件能有利於光學系統之色像差降低。 再者,特別是阿貝數(νd
)較小之區域中,一般的玻璃之部分分散比(θg,F)處於較正規線高之值,橫軸取阿貝數(νd
)、縱軸取部分分散比(θg,F)時一般的玻璃之部分分散比(θg,F)與阿貝數(νd
)之關係由較正規線斜率較大之曲線表示。上述之部分分散比(θg,F)與阿貝數(νd
)之關係式中,表示藉由使用較正規線斜率較大之直線規定該等之關係,能獲得部分分散比(θg,F)較一般的玻璃小之玻璃。 本案發明中,表面法耐候性以具有較佳為級1或級2、更佳為級1為佳。 此處,所謂表面法耐候性係使用以下之試驗方法進行。 使用具有30 mm×30 mm×3 mm研磨面之試樣作為試驗片,置於60℃相對濕度95%之恆溫恆濕槽中96小時之後,藉由50倍之顯微鏡觀察研磨面以觀察變色之狀態。判定基準係將藉由照度1500勒克斯觀察試驗96小時後之試樣時完全未發現變色者設為級1,將藉由100勒克斯觀察時未發現變色但藉由1500勒克斯能發現者設為級2,將藉由100勒克斯觀察時能發現變色者設為級3。再者,關於級3,重新置於50℃相對濕度85%之恆溫恆濕槽中6小時之後,藉由50倍之顯微鏡觀察研磨面,將藉由1500勒克斯能發現變色者設為級4。未發現變色之情形時仍視為級3。 再者,於本說明書中,所謂「表面法耐候性」係表示例如作為透鏡預成形材而長期使用之情形或因光學玻璃之保管環境而曝露一定期間之情形時之變色狀態之優劣。 本發明之光學玻璃較佳為著色較少。 特別是,本發明之光學玻璃若以玻璃之透過率表示,則於厚度10 mm之樣品中表示分光透過率80%之波長(λ80
)較佳為420 nm以下,更佳為400 nm以下,進而較佳為380 nm以下。 又,本發明之光學玻璃於厚度10 mm之樣品中表示分光透過率5%之波長(λ5
)較佳為365 nm以下,更佳為345 nm以下,進而較佳為330 nm以下。 藉此,玻璃之吸收端變得位於紫外區域之附近,可見區域之玻璃之透明性提高,故能夠較佳地使用該光學玻璃作為透鏡等光學元件之材料。 又,本發明之光學玻璃之耐失透性需要較高。藉此,能抑制因玻璃製作時之玻璃之結晶化等所導致之透過率之降低,故能夠較佳地使用該光學玻璃作為透鏡等使可見光透過之光學元件。特別是,本發明之光學玻璃較佳為具有1200℃以下之低液相溫度。更具體而言,本發明之光學玻璃之液相溫度係將較佳為1200℃、更佳為1150℃、更佳為1100℃、更佳為1050℃作為上限。藉此,即便熔融玻璃以更低之溫度流出,亦能降低所製作之玻璃之結晶化,故能夠提高自熔融狀態形成玻璃時之耐失透性,能夠降低對使用玻璃之光學元件之光學特性之影響。另一方面,本發明之光學玻璃之液相溫度之下限無特別限定,藉由本發明所獲得之玻璃之液相溫度多為大致500℃以上,具體而言550℃以上,進而具體而言600℃以上。再者,本說明書中之所謂「液相溫度」係將粉碎為直徑2 mm左右之粒狀之玻璃試樣載置於鉑板上,於具有800℃至1220℃之溫度梯度之爐內保持30分鐘後取出,冷卻後利用倍率80倍之顯微鏡觀察玻璃中有無結晶,藉此而測定之於玻璃中未發現結晶且未產生失透之最低溫度。 [預成形體及光學元件] 能夠自所製作之光學玻璃使用例如再熱壓成形或精密壓製成形等鑄模壓製成形之手段而製作玻璃成形體。即,自光學玻璃製作鑄模壓製成形用之預成形體,對該預成形體進行再熱壓成形後進行研磨加工而製作玻璃成形體,或對例如進行研磨加工所製作之預成形體進行精密壓製成形來製作玻璃成形體。再者,製作玻璃成形體之手段不限定於該等手段。 以如此之方式製作之玻璃成形體對多種光學元件有用,其中,特佳為用於透鏡或稜鏡等光學元件之用途。藉此,設有光學元件之光學系統之透過光中之因色像差所導致之滲色降低。因此,將該光學元件用於相機之情形時能夠更準確地表現攝影對象物,將該光學元件用於投影機之情形時能夠更高精彩地投影所需之影像。 [實施例] 將本發明之實施例(No.A1~No.A28、No.B1~No.B52、No.C1~C3)及比較例(No.a、No.b)之組成、以及折射率(nd
)、阿貝數(νd
)、部分分散比(θg,F)、分光透過率示為5%及80%之波長(λ5
、λ80
)、液相溫度、表面法耐候性之結果示於表1~表12。此處,實施例(No.A1~No.A28、No.C1~C3)亦可為第1光學玻璃之實施例,實施例(No.B1~No.B52、No.C1~C3)亦可為第2光學玻璃之實施例。再者,以下之實施例始終為例示之目的,並非僅限定於該等實施例。 實施例及比較例之玻璃均以如下方式製作:作為各成分之原料,選定分別相當之氧化物、氫氧化物、碳酸鹽、硝酸鹽、氟化物、氫氧化物、偏磷酸化合物等用於通常之光學玻璃之高純度原料,以成為表中所示之各實施例及比較例之組成之比例之方式稱量且均勻地混合之後,投入至石製坩堝(根據玻璃之熔融性亦可使用鉑坩堝、氧化鋁坩堝),根據玻璃組成之熔融難易度,藉由電爐於1100~1400℃之溫度範圍熔解0.5~5小時之後,移至鉑坩堝予以攪拌均質化而進行消泡等之後,使溫度降低至1000~1400℃且予以攪拌均質化之後澆鑄入模具中,緩冷而製作玻璃。 實施例及比較例之玻璃之折射率(nd
)、阿貝數(νd
)及部分分散比(θg,F)係基於日本光學玻璃工業會標準JOGIS01-2003而測定。 再者,用於本測定之玻璃係使用將緩冷降溫速度設為-25℃/hr、且已於退火爐中進行處理者。 實施例及比較例之表面法耐候性藉由以下方法進行評價。 使用具有30 mm×30 mm×3 mm研磨面之試樣作為試驗片,置於60℃相對濕度95%之恆溫恆濕槽中96小時之後,藉由50倍之顯微鏡觀察研磨面以觀察變色之狀態。判定基準係將藉由照度1500勒克斯觀察試驗96小時後之試樣時完全未發現變色者設為級1,將藉由100勒克斯觀察時未發現變色但藉由1500勒克斯能發現者設為級2,將藉由100勒克斯觀察時能發現變色者設為級3。再者,關於級3,重新置於50℃相對濕度85%之恆溫恆濕槽中6小時之後,藉由50倍之顯微鏡觀察研磨面,將藉由1500勒克斯能發現變色者設為級4。未發現變色之情形時仍視為級3。 實施例及比較例之玻璃之透過率係根據日本光學玻璃工業會標準JOGIS02而測定。再者,於本發明中,藉由測定玻璃之透過率,求出玻璃之著色之有無及程度。具體而言,將厚度10±0.1 mm之對面平行研磨品根據JISZ8722而測定200~800 nm之分光透過率,求出λ5
(透過率5%時之波長)及λ80
(透過率80%時之波長)。 實施例及比較例之液相溫度係藉由將粉碎之玻璃試樣以10 mm間隔載置於鉑板上,將其於具有800℃至1200℃之溫度梯度之爐內保持30分鐘後取出,冷卻後利用倍率80倍之顯微鏡觀察玻璃試樣中結晶之有無而進行測定。此時,將光學玻璃粉碎為直徑2 mm左右之粒狀作為樣品。 [表1]
[表2]
[表3]
[表4]
[表5]
[表6]
[表7]
[表8]
[表9]
[表10]
[表11]
[表12]
如該等表所示,本發明之實施例之光學玻璃之部分分散比(θg,F)與阿貝數(νd
)滿足(-0.00256×νd
+0.637)≦(θg,F)≦(-0.00256×νd
+0.684)之關係,更詳細而言,滿足(-0.00256×νd
+0.657)≦(θg,F)≦(-0.00256×νd
+0.679)之關係。特別是,實施例(No.B1~No.B52、No.C1~C3)之光學玻璃滿足(-0.00256×νd
+0.657)≦(θg,F)≦(-0.00256×νd
+0.677)之關係。此處,關於本案實施例之玻璃之部分分散比(θg,F)與阿貝數(νd
)之關係如圖2所示。 本發明之實施例之光學玻璃之折射率(nd
)均為1.60以上,更詳細而言為1.65以上,並且該折射率(nd
)為1.78以下,更詳細而言為1.76以下,為所需範圍內。特別是,實施例(No.A1~No.A28、No.C1~C3)之光學玻璃之折射率(nd
)為1.75以下,更詳細而言為1.73以下。 又,本發明之實施例之光學玻璃之阿貝數(νd
)均為28以上,更詳細而言為30以上,為所需範圍內。又,本發明之實施例之光學玻璃之阿貝數(νd
)為47以下,更詳細而言為46以下,為所需範圍內。特別是,實施例(No.A1~No.A28、No.C1~C3)之光學玻璃之阿貝數(νd
)為43以下。 此外,本發明之實施例之光學玻璃之λ80
(透過率80%時之波長)均為420 nm以下,更詳細而言為400 nm以下。特別是,實施例(No.A1~No.A28、No.C1~C3)之光學玻璃之λ80
(透過率80%時之波長)為390 nm以下。 又,本發明實施例之光學玻璃之λ5
(透過率5%時之波長)都為365 nm以下,更詳細而言,為345 nm以下,進而詳細地為340 nm以下。特別是,實施例(No.A1~No.A28、No.C1~C3)之光學玻璃之λ5
(透過率5%時之波長)為335 nm以下。 由此可知,本發明之實施例之光學玻璃相對於可見光之透過率較高而不易著色。 此外,本發明之實施例(No.A1~No.A28、No.C1~C3)之光學玻璃之液相溫度為1200℃以下,更詳細而言為1110℃以下,進而詳細而言為1050℃以下。因此,該等光學玻璃不易引起因再加熱所導致之失透或乳白,故推測具有高再熱壓成形性。 又,本發明實施例(No.B1~No.B52、No.C1~C3)之光學玻璃之表面法耐候性為級1。 因此,明確可知,該等光學玻璃係表面法耐候性優異且不易產生所謂之變色之光學玻璃。 進而,使用本發明之實施例之光學玻璃而形成玻璃塊,對該玻璃塊進行研削及研磨,加工成透鏡及稜鏡之形狀。其結果能夠穩定地加工成各種透鏡及稜鏡之形狀。 再者,比較例(No.b)所記載之光學玻璃雖然滿足所需光學常數(nd
、νd
),但由於部分分散比較大而異常分散性較小,並且透過率亦較差,化學耐久性亦較差,故無法獲得本案發明中作為目標的、折射率(nd
)及阿貝數(νd
)處於所需之範圍內並且部分分散比(θg,F)較小且表面法耐候性良好之光學玻璃。 以上,基於例示之目的而對本發明進行詳細說明,但請理解本實施例始終僅為例示之目的,能夠由業者在不脫離本發明之思想及範圍之情況下完成多種改變。The optical glass of the present invention contains 20.0-60.0% of SiO 2 component and 10.0-50.0% of Nb 2 O 5 component based on the mass% of oxide conversion composition, and the partial dispersion ratio (θg, F) is equal to the Abbe number ( ν d ) satisfy the relationship of (-0.00256×ν d +0.637)≦(θg,F)≦(-0.00256×ν d +0.684). In the glass containing SiO 2 component and Nb 2 O 5 component, a glass with high refractive index or low Abbe number (high dispersion) and low partial dispersion ratio within the required range can be obtained. Therefore, it is possible to obtain an optical glass that has the required high refractive index (n d ) and low Abbe number (ν d ) and has a small partial dispersion ratio (θg, F), which is useful for reducing the chromatic aberration of the optical system. In particular, the first optical glass contains 20.0-60.0% of SiO 2 component, 20.0-45.0% of Nb 2 O 5 component, 1.0-20.0% of ZrO 2 component, and has 1.60 or more The refractive index (n d ) below 1.75 and the Abbe number (ν d ) above 30 and 47 below, the partial dispersion ratio (θg, F) and the Abbe number (ν d ) satisfy (-0.00256×ν d +0) .637)≦(θg,F)≦(-0.00256×ν d +0.684). In the first optical glass, in a glass containing SiO 2 component, Nb 2 O 5 component and ZrO 2 component, a high refractive index or low Abbe number (high dispersion) and low partial dispersion ratio within the required range can be obtained Of glass. Therefore, it is possible to obtain an optical glass that has the required high refractive index (n d ) and low Abbe number (ν d ) and has a small partial dispersion ratio (θg, F), which is useful for reducing the chromatic aberration of the optical system. In addition, the second optical glass contains 20.0-60.0% of SiO 2 component, 10.0-50.0% of Nb 2 O 5 component, and more than 0.1 to 15.0% of K 2 O component in terms of mass% of oxide conversion composition. The dispersion ratio (θg, F) satisfies the relationship between (-0.00256×ν d +0.637)≦(θg,F)≦(-0.00256×ν d +0.684) and the Abbe number (ν d ). The surface Method weather resistance is level 1 or 2. In the second optical glass, in a glass containing SiO 2 component, Nb 2 O 5 component, and K 2 O component, a high refractive index or low Abbe number (high dispersion) and low partial dispersion within the required range can be obtained Compared with glass, especially by containing the K 2 O component, the adjustment of the required optical constants becomes easier, and it is possible to reduce the occurrence of discoloration while keeping the partial dispersion ratio (θg, F) small. Therefore, it is possible to obtain the following optical glass, which has the required high refractive index (n d ) and low Abbe number (ν d ), and the partial dispersion ratio (θg, F) is small, which affects the chromatic aberration of the optical system Reduction is useful, and chemical durability, especially surface method weather resistance is good. Hereinafter, the embodiment of the optical glass of the present invention will be described in detail. The present invention is not limited to the following embodiments at all, and can be implemented with appropriate additions and changes within the scope of the object of the present invention. In addition, the description may be omitted as appropriate for the overlapping descriptions, but this does not limit the gist of the invention. [Glass component] The composition range of each component constituting the optical glass of the present invention will be described below. When there is no special description in this manual, the content of each component is expressed by mass% relative to the total mass of the glass in terms of all oxides. Here, the so-called "oxide conversion composition" is when it is assumed that the oxides, composite salts, metal fluorides, etc. used as the raw materials of the glass constituents of the present invention are all decomposed into oxides during melting. The total mass of oxides is set to 100% by mass, indicating the composition of each component contained in the glass. <Regarding essential components and optional components> The SiO 2 component is an essential component that promotes stable glass formation and lowers the liquidus temperature, thereby reducing the devitrification (generation of crystals) which is undesirable as an optical glass. In particular, by making the content of the SiO 2 component 20.0% or more, it is possible to obtain a glass having excellent devitrification resistance without greatly increasing the partial dispersion ratio. In addition, it is possible to reduce devitrification or coloration during glass formation or reheating. Therefore, the content of the SiO 2 component is preferably 20.0%, more preferably 23.0%, still more preferably 25.0%, still more preferably 27.0%, still more preferably 30.0%, still more preferably 32.0% as the lower limit . On the other hand, by making the content of the SiO 2 component 60.0% or less, the refractive index is not easily lowered, so that the required high refractive index can be easily obtained, and the increase in the partial dispersion ratio can be suppressed. In addition, it is possible to suppress the decrease in the melting properties of the glass raw material by this. Therefore, the content of the SiO 2 component will be preferably 60.0%, more preferably 55.0%, still more preferably 50.0%, still more preferably 48.0%, still more preferably 47.0%, still more preferably 45.0%, and further It is preferably 44.0%, and more preferably 43.0% as the upper limit. As the SiO 2 component, SiO 2 , K 2 SiF 6 , Na 2 SiF 6 or the like can be used as a raw material. The Nb 2 O 5 component is an essential component that can increase the refractive index, reduce the Abbe number and partial dispersion ratio, and improve the devitrification resistance. In particular, by setting the content of the Nb 2 O 5 component to 10.0% or more, the refractive index can be increased and the optical constant can be adjusted to the target within the components within the scope of the present invention, thereby reducing the abnormal dispersibility. Therefore, the content of the Nb 2 O 5 component is preferably 10.0%, more preferably 15.0%, still more preferably 20.0%, more preferably 22.0%, and still more preferably 23.0% as the lower limit. On the other hand, by making the content of the Nb 2 O 5 component 50.0% or less, the material cost of the glass can be reduced. In addition, it is possible to suppress the increase in the melting temperature during glass production and reduce the devitrification caused by the excessive inclusion of the Nb 2 O 5 component. Furthermore, the chemical durability of the glass can also be deteriorated and improved. Therefore, the content of the Nb 2 O 5 component will be preferably 50.0%, more preferably 45.0%, still more preferably 43.0%, still more preferably 41.5%, still more preferably 40.0%, still more preferably 35.0% , And more preferably 30.0% as the upper limit. For the Nb 2 O 5 component, Nb 2 O 5 or the like can be used as a raw material. The ZrO 2 component is a component that can increase the refractive index and Abbe number of the glass, reduce the partial dispersion ratio, and improve the devitrification resistance when it contains more than 0%. It is an essential component especially in the first optical glass. In addition, by containing the ZrO 2 component, it is possible to reduce devitrification or coloration during glass formation or reheating. Therefore, the content of the ZrO 2 component may also be preferably 1.0% or more, more preferably more than 1.0%, still more preferably more than 3.0%, and still more preferably more than 5.0%. On the other hand, by making the content of the ZrO 2 component 20.0% or less, devitrification can be reduced, and a more homogeneous glass can be easily obtained. Therefore, the content of the ZrO 2 component is preferably 20.0%, more preferably 18.0%, still more preferably 15.0%, still more preferably 13.0%, and still more preferably 10.0% as the upper limit. The ZrO 2 component can use ZrO 2 , ZrF 4, etc. as a raw material. The K 2 O component is an optional component that can improve the solubility of the glass raw material and lower the liquidus temperature when the content exceeds 0%. Especially in the second optical glass, the K 2 O component is an essential component that can improve the chemical durability. In particular, by containing the content of the K 2 O component exceeding 0%, the discoloration in the glass can be effectively improved. Therefore, the content of the K 2 O component may preferably exceed 0%, more preferably exceed 0.1%, still more preferably exceed 0.3%, still more preferably exceed 0.5%, and still more preferably exceed 1.0%. On the other hand, by making the content of the K 2 O component 15.0% or less, the increase in the partial dispersion ratio can be suppressed, the devitrification can be reduced, and the chemical durability can be made difficult to deteriorate. Therefore, the content of the K 2 O component is preferably 15.0% or less, more preferably 10.0% or less, still more preferably less than 10.0%, still more preferably less than 8.0%, and still more preferably less than 5.0%. The K 2 O component can use K 2 CO 3 , KNO 3 , KF, KHF 2 , K 2 SiF 6 or the like as a raw material. The ZnO component is an optional component that is inexpensive and can improve the devitrification resistance when it contains more than 0%, and can reduce the glass transition point. Therefore, the content of the ZnO component may also preferably exceed 0%, more preferably exceed 0.5%, and still more preferably exceed 1.0%. On the other hand, by making the content of the ZnO component 25.0% or less, devitrification or coloring during glass formation or reheating can be reduced, and chemical durability can be improved. Therefore, the content of the ZnO component is preferably 25.0% or less, more preferably 20.0% or less, still more preferably less than 18.0%, still more preferably less than 14.0%, still more preferably less than 13.0%, and more preferably It is less than 10.0%. The Li 2 O component is an optional component that can reduce the partial dispersion ratio, improve the transmittance, lower the liquidus temperature, and improve the solubility of the glass raw material when the content exceeds 0%. Therefore, the content of the Li 2 O component may preferably exceed 0%, more preferably exceed 1.0%, still more preferably exceed 3.0%, and still more preferably exceed 5.0%. On the other hand, by making the content of the Li 2 O component 20.0% or less, the decrease in the refractive index can be suppressed, the chemical durability can be made difficult to deteriorate, and the devitrification caused by excessive content can be reduced. Therefore, the content of the Li 2 O component is preferably 20.0% or less, more preferably 15.0% or less, still more preferably 13.0% or less, still more preferably less than 10.0%, and still more preferably less than 8.0%. As the Li 2 O component, Li 2 CO 3 , LiNO 3 , LiF, etc. can be used as a raw material. The Na 2 O component is an optional component that can reduce the partial dispersion ratio, lower the liquidus temperature, and improve the solubility of the glass raw material when the content exceeds 0%. Therefore, the content of the Na 2 O component may preferably exceed 0%, more preferably exceed 1.0%, still more preferably exceed 3.0%, and still more preferably exceed 5.0%. On the other hand, by making the content of the Na 2 O component 20.0% or less, the decrease in refractive index can be suppressed, the chemical durability can be made difficult to deteriorate, and the devitrification caused by excessive content can be reduced. Therefore, the content of the Na 2 O component is preferably 20.0% or less, more preferably 15.0% or less, still more preferably 13.0% or less, still more preferably less than 10.0%, and still more preferably less than 8.0%. For the Na 2 O component, Na 2 CO 3 , NaNO 3 , NaF, Na 2 SiF 6 or the like can be used as a raw material. The B 2 O 3 component is an optional component as follows: when it contains more than 0%, it can promote stable glass formation, and can lower the liquidus temperature, so it can improve the resistance to devitrification and improve the melting of the glass raw material sex. Therefore, the content of the B 2 O 3 component may preferably exceed 0%, more preferably exceed 0.1%, still more preferably exceed 1.0%, still more preferably exceed 3.0%, and still more preferably exceed 5.0%. In particular, from the viewpoint of improving the resistance to devitrification and reducing the veins of molten glass formed at low temperature, it is more preferable to contain 3.0% or more of B 2 O 3 component, and it can also be more preferably 5.0% or more, and more preferably It is more than 7.0%. On the other hand, by making the content of the B 2 O 3 component 20.0% or less, the decrease in refractive index can be suppressed, and the increase in the partial dispersion ratio can be suppressed. Furthermore, the deterioration of the chemical durability of the glass can also be improved. Therefore, the content of the B 2 O 3 component is preferably 20.0%, more preferably 18.0%, still more preferably 15.0%, and still more preferably 12.0% as the upper limit. For the B 2 O 3 component, H 3 BO 3 , Na 2 B 4 O 7 , Na 2 B 4 O 7 ·10H 2 O, BPO 4, etc. can be used as raw materials. The TiO 2 component is an optional component that increases the refractive index, decreases the Abbe number, and improves the resistance to devitrification when the content exceeds 0%. On the other hand, by making the content of the TiO 2 component 15.0% or less, the coloring of the glass can be reduced, and the internal transmittance can be improved. In addition, by this, the partial dispersion ratio is not easily increased, so that the required low partial dispersion ratio close to the normal line can be easily obtained. Therefore, the content of the TiO 2 component is preferably 15.0% or less, more preferably 10.0% or less, still more preferably 5.0% or less, still more preferably less than 5.0%, still more preferably less than 3.0%, and more preferably It is 2.0% or less, more preferably less than 1.0%. In particular, from the viewpoint of reducing the abnormal dispersibility of the glass, it is preferable to not contain it substantially. As the TiO 2 component, TiO 2 or the like can be used as a raw material. The MgO component is any component that can lower the melting temperature of the glass when the content exceeds 0%. On the other hand, by making the content of the MgO component 10.0% or less, the decrease in refractive index can be suppressed and devitrification can be reduced. Therefore, the content of the MgO component is preferably 10.0% or less, more preferably less than 5.0%, still more preferably less than 3.0%, and still more preferably less than 1.0%. The MgO component can use MgO, MgCO 3 , MgF 2 or the like as a raw material. The CaO component is an optional component that can reduce the material cost of the glass, reduce the Abbe number, reduce the devitrification, and improve the solubility of the glass raw material when it contains more than 0%. Therefore, the content of the CaO component may preferably exceed 0%, more preferably exceed 1.0%, and still more preferably exceed 2.0%. On the other hand, by making the content of the CaO component 10.0% or less, the decrease in refractive index, the increase in Abbe number, and the increase in partial dispersion ratio can be suppressed, and devitrification can be reduced. Therefore, the content of the CaO component is preferably 10.0% or less, more preferably less than 5.0%, still more preferably less than 3.0%, and still more preferably less than 1.0%. CaO component can be used CaCO 3, CaF 2 and the like as a raw material. The SrO component is an optional component that can increase the refractive index and increase the resistance to devitrification when it contains more than 0%. In particular, by making the content of the SrO component 10.0% or less, the deterioration of chemical durability can be suppressed. Therefore, the content of the SrO component is preferably 10.0% or less, more preferably less than 5.0%, still more preferably 3.0% or less, still more preferably less than 3.0%, and still more preferably less than 1.0%. For the SrO component, Sr(NO 3 ) 2 , SrF 2 or the like can be used as a raw material. The BaO component is an optional component as follows: when it contains more than 0%, it can increase the refractive index, reduce the partial dispersion ratio, improve the resistance to devitrification, and improve the solubility of the glass raw material, and compared with other alkaline earth components , Can reduce the material cost of glass. In particular, by making the content of the BaO component 10.0% or less, the decrease in refractive index, the increase in Abbe number, and the increase in partial dispersion ratio can be suppressed, and devitrification can be reduced. Therefore, the content of the BaO component is preferably 10.0% or less, more preferably less than 5.0%, still more preferably less than 3.0%, and still more preferably less than 1.0%. The BaO component can use BaCO 3 , Ba(NO 3 ) 2 and the like as a raw material. The La 2 O 3 component, the Gd 2 O 3 component, the Y 2 O 3 component, and the Yb 2 O 3 component are optional components that can increase the refractive index and reduce the partial dispersion ratio by containing at least one of more than 0%. In particular, by setting the content of each of the La 2 O 3 component, Gd 2 O 3 component, Y 2 O 3 component, and Yb 2 O 3 component to 10.0% or less, the increase in Abbe number can be suppressed and devitrification can be reduced. And can reduce material costs. Therefore, the content of each of the La 2 O 3 component, Gd 2 O 3 component, Y 2 O 3 component, and Yb 2 O 3 component is preferably 10.0%, more preferably 5.0%, and still more preferably 3.0% as the upper limit. , And more preferably less than 1.0%. La 2 O 3 components, Gd 2 O 3 components, Y 2 O 3 components, and Yb 2 O 3 components can be used La 2 O 3 , La(NO 3 ) 3・XH 2 O (X is any integer), Y 2 O 3. YF 3 , Gd 2 O 3 , GdF 3 , Yb 2 O 3 and the like are used as raw materials. When the content of Ta 2 O 5 exceeds 0%, it is an optional component that increases the refractive index, reduces the Abbe number and partial dispersion ratio, and improves the resistance to devitrification. On the other hand, by making the content of Ta 2 O 5 component 10.0% or less, the amount of Ta 2 O 5 component used as a rare mineral resource is reduced, and the glass becomes easier to melt at low temperature, so the production of glass can be reduced cost. In addition, it is possible to reduce the devitrification of the glass due to the excessive content of the Ta 2 O 5 component. Therefore, the content of the Ta 2 O 5 component is preferably 10.0% or less, more preferably less than 5.0%, still more preferably less than 3.0%, and still more preferably less than 1.0%. Especially from the viewpoint of reducing the material cost of glass, the Ta 2 O 5 component may not be included. For the Ta 2 O 5 component, Ta 2 O 5 or the like can be used as a raw material. The WO 3 component is an optional component that increases the refractive index and lowers the Abbe number when it contains more than 0%, improves the devitrification resistance, and can improve the meltability of the glass raw material. On the other hand, by making the content of the WO 3 component 10.0% or less, the partial dispersion ratio of the glass can not be easily increased, and the coloring of the glass can be reduced and the internal transmittance can be improved. Therefore, the content of the WO 3 component is preferably 10.0% or less, more preferably less than 5.0%, still more preferably less than 3.0%, and still more preferably less than 1.0%. For the WO 3 component, WO 3 or the like can be used as a raw material. The P 2 O 5 component is an optional component that can improve the stability of the glass when the content exceeds 0%. On the other hand, by making the content of the P 2 O 5 component 10.0% or less, it is possible to reduce the devitrification caused by the excessive inclusion of the P 2 O 5 component. Therefore, the content of the P 2 O 5 component is preferably 10.0% or less, more preferably less than 5.0%, still more preferably less than 3.0%, and still more preferably less than 1.0%. The P 2 O 5 component can use Al(PO 3 ) 3 , Ca(PO 3 ) 2 , Ba(PO 3 ) 2 , BPO 4 , H 3 PO 4, etc. as raw materials. The GeO 2 component is an optional component that increases the refractive index and reduces devitrification when the content exceeds 0%. On the other hand, by making the content of the GeO 2 component 10.0% or less, the usage amount of the expensive GeO 2 component can be reduced, so that the material cost of the glass can be reduced. Therefore, the content of the GeO 2 component is preferably 10.0% or less, more preferably less than 5.0%, still more preferably less than 3.0%, and still more preferably less than 1.0%. The GeO 2 component can use GeO 2 or the like as a raw material. The Al 2 O 3 component and the Ga 2 O 3 component are optional components that can improve chemical durability and increase resistance to devitrification when at least one of them exceeds 0%. On the other hand, by making the content of each of the Al 2 O 3 component and the Ga 2 O 3 component 10.0% or less, it is possible to reduce the devitrification caused by the excessive inclusion of the Al 2 O 3 component or the Ga 2 O 3 component. Therefore, the content of each of the Al 2 O 3 component and the Ga 2 O 3 component is preferably 10.0% or less, more preferably less than 5.0%, still more preferably less than 3.0%, and still more preferably less than 1.0%. The Al 2 O 3 component and the Ga 2 O 3 component can use Al 2 O 3 , Al(OH) 3 , AlF 3 , Ga 2 O 3 , Ga(OH) 3, etc. as raw materials. The Bi 2 O 3 component is an optional component that can increase the refractive index, lower the Abbe number, and lower the glass transition point when the content exceeds 0%. On the other hand, by making the content of the Bi 2 O 3 component 10.0% or less, the partial dispersion ratio can be prevented from increasing easily, and the coloring of the glass can be reduced to increase the internal transmittance. Therefore, the content of the Bi 2 O 3 component is preferably 10.0% or less, more preferably less than 5.0%, still more preferably less than 3.0%, and still more preferably less than 1.0%. For the Bi 2 O 3 component, Bi 2 O 3 or the like can be used as a raw material. The TeO 2 component is an optional component that can increase the refractive index, reduce the partial dispersion ratio, and reduce the glass transition point when the content exceeds 0%. On the other hand, by making the content of the TeO 2 component 5.0% or less, the coloring of the glass can be reduced and the internal transmittance can be improved. In addition, by reducing the use of expensive TeO 2 components, glass with lower material cost can be obtained. Therefore, the content of the TeO 2 component is preferably 5.0% or less, more preferably less than 3.0%, and still more preferably less than 1.0%. For the TeO 2 component, TeO 2 or the like can be used as a raw material. The SnO 2 component is an optional component that can clarify (defoam) the molten glass and increase the visible light transmittance of the glass when it contains more than 0%. On the other hand, by making the content of the SnO 2 component 1.0% or less, it is possible to make the coloring of the glass due to the reduction of the molten glass or the devitrification of the glass less likely to occur. In addition, since the alloying between the SnO 2 component and the melting equipment (especially noble metals such as Pt) is reduced, the life of the melting equipment can be increased. Therefore, the content of the SnO 2 component is preferably 1.0% or less, more preferably less than 0.5%, and still more preferably less than 0.1%. For the SnO 2 component, SnO, SnO 2 , SnF 2 , SnF 4, etc. can be used as a raw material. The Sb 2 O 3 component is a component that promotes the defoaming of the glass and clarifies the glass when the content exceeds 0%, and is an optional component in the optical glass of the present invention. By making the content of Sb 2 O 3 relative to the total mass of the glass 1.0% or less, excessive foaming during glass melting can be prevented, and the Sb 2 O 3 component can be difficult to alloy with melting equipment (especially precious metals such as Pt) change. Therefore, the content rate of the Sb 2 O 3 component relative to the total mass of the glass in the oxide conversion composition is preferably 1.0%, more preferably 0.8%, and still more preferably 0.6% as the upper limit. Here, especially from the viewpoint of easily obtaining optical glass with low exposure effect, the content of the Sb 2 O 3 component in the total glass mass of the oxide-converted composition is preferably 0.5%, more preferably 0.3%, and further Preferably, it is 0.1% as the upper limit. In addition, the component for clarifying and defoaming glass is not limited to the above-mentioned Sb 2 O 3 component, and a well-known clarifier or defoamer in the field of glass manufacturing, or a combination thereof can be used. The ratio of the sum of the contents of the Li 2 O component and the K 2 O component to the sum of the contents of the ZrO 2 component and the Li 2 O component is preferably more than 0 and less than 2.5. In particular, by setting the mass ratio to exceed 0, devitrification and transmittance can be improved. Therefore, the lower limit of (Li 2 O+K 2 O)/(ZrO 2 +Li 2 O) can preferably exceed 0, more preferably exceed 0.1, and still more preferably exceed 0.3. On the other hand, by setting the mass ratio to less than 2.5, it is possible to reduce the abnormal dispersion of the glass while maintaining the refractive index of the glass. Therefore, the upper limit of (Li 2 O+K 2 O)/(ZrO 2 +Li 2 O) may also preferably be less than 2.5, more preferably less than 2.1, more preferably less than 2.0, and more preferably less than 1.5, more preferably less than 1.0, and still more preferably less than 0.5. The total (mass sum) of the SiO 2 component and the Nb 2 O 5 component is preferably more than 50.0%. Thereby, it is possible to obtain a glass that has excellent chemical durability, less abnormal dispersion, maintains a certain degree of viscosity, and has good moldability. Therefore, the mass sum may preferably exceed 50.0%, more preferably 53.0% or more, still more preferably 54.0% or more, and still more preferably 58.0% or more. On the other hand, the mass sum may also be preferably 90.0% or less, more preferably less than 85.0%, still more preferably less than 81.0%, and still more preferably less than 76.0%. The total content (mass sum) of the Ln 2 O 3 component (in the formula, Ln is one or more selected from the group consisting of La, Gd, Y, and Yb) is preferably 15.0% or less. Thereby, the devitrification of the glass can be reduced, the increase in the Abbe number can be suppressed, and the material cost of the glass can be reduced. Therefore, the mass sum of the Ln 2 O 3 components is preferably 15.0% or less, more preferably less than 10.0%, still more preferably less than 5.0%, and still more preferably less than 3.5%. By making the total content (mass sum) of the Rn 2 O component (in the formula, Rn is one or more selected from the group consisting of Li, Na, and K) more than 0%, the solubility of the glass raw material can be improved , And reduce the glass transfer point. Therefore, the content of the Rn 2 O component may also preferably exceed 0%, more preferably 5.0% or more, still more preferably more than 5.0%, still more preferably 8.0% or more, still more preferably 10.0% or more, and more It is preferably more than 10.0%, more preferably 12.0% or more, and still more preferably more than 13.0%. On the other hand, the total content (mass sum) of the Rn 2 O component (in the formula, Rn is one or more selected from the group consisting of Li, Na, and K) is preferably 30.0% or less. Thereby, the refractive index of the glass can be prevented from being lowered, and the devitrification of the glass can be reduced when the glass is formed. In addition, it can reinforce the viscosity in the glass and improve the formability. Therefore, the total content of the Rn 2 O components is preferably 30.0%, more preferably 25.0%, still more preferably 20.0%, and still more preferably 17.0% as the upper limit. The total content (mass sum) of the RO component (in the formula, R is one or more selected from the group consisting of Mg, Ca, Sr, and Ba) is preferably 30.0% or less. Thereby, it is possible to reduce the devitrification of the glass caused by the excessive inclusion of these components. Therefore, the mass sum of the RO component is preferably 30.0% or less, more preferably 25.0% or less, still more preferably 20.0% or less, still more preferably 15.0% or less, still more preferably less than 10.0%, and more preferably Less than 5.0%. On the other hand, the quality of the RO component and the viewpoint of improving the solubility of the glass raw material and reducing devitrification may also preferably exceed 0%, more preferably 1.0% or more, and even more preferably 2.0% or more. <About the components that should not be contained> Next, the components that should not be contained in the optical glass of the present invention and the components that are undesirable if contained. Other ingredients can be added as needed within the range that does not impair the characteristics of the glass of the present invention. However, in addition to Ti, Zr, Nb, W, La, Gd, Y, Yb, Lu, V, Cr, Mn, Fe, Co, Ni, Cu, Ag, and Mo and other transition metal components have even if singly or in combination Containing a small amount of each of them will also color the glass and absorb specific wavelengths in the visible region of the visible region. Therefore, especially in optical glass that uses wavelengths in the visible region, it is preferably not contained substantially. In addition, lead compounds such as PbO and arsenic compounds such as As 2 O 3 are components that have a high environmental impact and are therefore preferably not contained substantially, that is, they are not contained except for unavoidable mixing. Furthermore, the components of Th, Cd, Tl, Os, Be, and Se have been used as hazardous chemicals in recent years, and their use has tended to be controlled. Not only the glass manufacturing steps, but also the processing steps, and the processing after productization are required Measures on environmental countermeasures. Therefore, when attaching importance to environmental impacts, it is preferable that these are not contained substantially. [Manufacturing method] The optical glass of the present invention is manufactured as follows, for example. That is, it is produced by the following steps: the above-mentioned raw materials are uniformly mixed in such a way that each component is within a specific content range, the produced mixture is put into a platinum crucible, a quartz crucible or an alumina crucible for rough melting, and then a gold Melt in the crucible, platinum crucible, platinum alloy crucible or iridium crucible in the temperature range of 1000~1400℃ for 3~5 hours, stir and homogenize for defoaming, etc., then cool to 900~1100℃, then perform fine stirring to Remove the veins, cast into the mold and slowly cool. <Physical properties> The optical glass of the present invention has a high refractive index and an Abbe number in a specific range. The refractive index (n d ) of the optical glass of the present invention is preferably 1.60, more preferably 1.63, and even more preferably 1.65 as the lower limit. The upper limit of the refractive index is preferably 1.78, more preferably 1.77, still more preferably 1.76, still more preferably 1.75, still more preferably 1.73, and still more preferably 1.70. The Abbe number (ν d ) of the optical glass of the present invention is preferably 28, more preferably 29, still more preferably 30, still more preferably 31, and still more preferably 33 as the lower limit. On the other hand, the Abbe number (ν d ) of the optical glass of the present invention is preferably 47, more preferably 45, still more preferably 43, still more preferably 42, further preferably 41, and still more preferably Is 40 as the upper limit. The optical glass of the present invention having such a refractive index and Abbe number is useful in optical design, and in particular, can achieve high imaging characteristics, etc., and can also achieve miniaturization of the optical system, so that the degree of freedom of optical design can be expanded. The optical glass of the present invention has a low partial dispersion ratio (θg, F). More specifically, the partial dispersion ratio (θg, F) of the optical glass of the present invention, and the partial dispersion ratio (θg, F) of the optical glass of the present invention is preferably between the Abbe number (ν d ) Satisfy the relationship of (-0.00256×ν d +0.637)≦(θg,F)≦(-0.00256×ν d +0.684). Therefore, in the optical glass of the present invention, the partial dispersion ratio (θg, F) and Abbe number (ν d ) preferably satisfy the relationship of θg, F≧(-0.00256×ν d +0.637), and more preferably satisfy The relationship of θg, F≧(-0.00256×ν d +0.647), and more preferably satisfies the relationship of θg, F≧(-0.00256×ν d +0.657). On the other hand, in the optical glass of the present invention, the partial dispersion ratio (θg, F) and Abbe number (ν d ) preferably satisfy the relationship of θg, F≦(-0.00256×ν d +0.684), more preferably In order to satisfy the relationship of θg, F≦(-0.00256×ν d +0.681), it is more preferable to satisfy the relationship of θg, F≦(-0.00256×ν d +0.677). As a result, an optical glass with a low partial dispersion ratio (θg, F) can be obtained, so the optical element formed from the optical glass can help reduce the chromatic aberration of the optical system. Furthermore, especially in regions where the Abbe number (ν d ) is small, the partial dispersion ratio (θg, F) of general glass is higher than the normal line. The abscissa takes the Abbe number (ν d ) and the vertical When the axis takes the partial dispersion ratio (θg, F), the relationship between the partial dispersion ratio (θg, F) and Abbe number (ν d ) of general glass is represented by a curve with a larger slope than the normal line. The above-mentioned partial dispersion ratio (θg, F) and Abbe's number (ν d ) in the relational expressions indicate that the partial dispersion ratio (θg, F ) Smaller glass than ordinary glass. In the present invention, the weather resistance of the surface method is preferably grade 1 or grade 2, more preferably grade 1. Here, the so-called surface method weather resistance is performed using the following test method. Use a sample with a polished surface of 30 mm×30 mm×3 mm as a test piece, and place it in a constant temperature and humidity bath at 60°C with a relative humidity of 95% for 96 hours. Observe the polished surface with a 50-fold microscope to observe the discoloration state. The criterion is to observe the sample at 1500 lux with illuminance for 96 hours after no discoloration is found at level 1, and when observed at 100 lux, the discoloration is not found but can be detected at 1500 lux as level 2 , Set the person who can be found to be discolored when observed at 100 lux as level 3. In addition, for level 3, after re-placement in a constant temperature and humidity chamber at 50°C with a relative humidity of 85% for 6 hours, observe the polished surface with a 50-fold microscope, and set the color change that can be found by 1500 lux as level 4. If no discoloration is found, it will still be considered as level 3. In addition, in this specification, the term "surface method weather resistance" refers to the pros and cons of the discoloration state when used as a lens preform for a long time or when exposed to a certain period of time due to the storage environment of the optical glass. The optical glass of the present invention is preferably less colored. In particular, if the optical glass of the present invention is expressed in terms of the transmittance of the glass, the wavelength (λ 80 ) that represents 80% of the spectral transmittance in a sample with a thickness of 10 mm is preferably 420 nm or less, more preferably 400 nm or less, More preferably, it is 380 nm or less. In addition, the wavelength (λ 5 ) at which the optical glass of the present invention has a spectral transmittance of 5% in a sample with a thickness of 10 mm is preferably 365 nm or less, more preferably 345 nm or less, and still more preferably 330 nm or less. As a result, the absorption end of the glass becomes near the ultraviolet region, and the transparency of the glass in the visible region is improved. Therefore, the optical glass can be preferably used as a material for optical elements such as lenses. In addition, the devitrification resistance of the optical glass of the present invention needs to be high. Thereby, the decrease in transmittance due to the crystallization of the glass during glass production can be suppressed, so the optical glass can be preferably used as an optical element that transmits visible light, such as a lens. In particular, the optical glass of the present invention preferably has a low liquidus temperature of 1200°C or less. More specifically, the liquidus temperature of the optical glass of the present invention is preferably 1200°C, more preferably 1150°C, more preferably 1100°C, more preferably 1050°C as the upper limit. As a result, even if the molten glass flows out at a lower temperature, the crystallization of the glass produced can be reduced, so the resistance to devitrification when the glass is formed from the molten state can be improved, and the optical characteristics of the optical element using the glass can be reduced The impact. On the other hand, the lower limit of the liquidus temperature of the optical glass of the present invention is not particularly limited. Most of the liquidus temperature of the glass obtained by the present invention is approximately 500°C or higher, specifically 550°C or higher, and more specifically 600°C above. Furthermore, the so-called "liquid phase temperature" in this manual means that a glass sample crushed into a granular shape with a diameter of about 2 mm is placed on a platinum plate and maintained in a furnace with a temperature gradient of 800°C to 1220°C. Take it out in minutes, and observe whether there are crystals in the glass using a microscope with a magnification of 80 times after cooling, thereby measuring the lowest temperature at which no crystals are found in the glass and no devitrification occurs. [Preform and Optical Element] A glass molded body can be produced from the produced optical glass using mold compression molding methods such as re-hot press molding or precision press molding. That is, a preform for press molding of a mold is produced from optical glass, and the preform is re-hot-pressed and then polished to produce a glass molded body, or, for example, a preform produced by grinding is precision-pressed Molding to produce a glass molded body. In addition, the means for producing the glass molded body is not limited to these means. The glass molded body produced in this manner is useful for various optical elements, and among them, it is particularly preferably used for optical elements such as lenses or ridges. Thereby, the bleeding caused by chromatic aberration in the transmitted light of the optical system provided with the optical element is reduced. Therefore, when the optical element is used in a camera, the photographic object can be expressed more accurately, and when the optical element is used in a projector, the desired image can be projected more brilliantly. [Example] The composition and refraction of the examples of the present invention (No.A1~No.A28, No.B1~No.B52, No.C1~C3) and comparative examples (No.a, No.b) Rate (n d ), Abbe number (ν d ), partial dispersion ratio (θg, F), spectral transmittance shown as 5% and 80% of wavelength (λ 5 , λ 80 ), liquidus temperature, surface method weather resistance The results of the properties are shown in Table 1 to Table 12. Here, the examples (No.A1~No.A28, No.C1~C3) may be examples of the first optical glass, and the examples (No.B1~No.B52, No.C1~C3) may also be This is an example of the second optical glass. Furthermore, the following examples are always for the purpose of illustration, and are not limited to these examples. The glasses of the examples and comparative examples are made in the following way: as the raw materials of each component, the corresponding oxides, hydroxides, carbonates, nitrates, fluorides, hydroxides, metaphosphoric acid compounds, etc. are selected for general use. The high-purity raw materials of the optical glass are weighed and uniformly mixed in such a way as to become the composition ratio of each embodiment and comparative example shown in the table, and then put into a stone crucible (platinum can also be used according to the melting property of the glass Crucibles, alumina crucibles), according to the melting difficulty of the glass composition, melted in an electric furnace in the temperature range of 1100 to 1400°C for 0.5 to 5 hours, then moved to a platinum crucible to stir and homogenize for defoaming, etc., and then set the temperature It is lowered to 1000-1400°C and stirred and homogenized, then poured into a mold, and slowly cooled to produce glass. The refractive index (n d ), Abbe number (ν d ), and partial dispersion ratio (θg, F) of the glasses of the examples and comparative examples were measured based on the standard JOGIS01-2003 of the Optical Glass Industry Association of Japan. In addition, the glass used in this measurement is the one that has been processed in the annealing furnace with the slow cooling rate set to -25°C/hr. The surface method weather resistance of the examples and comparative examples was evaluated by the following method. Use a sample with a polished surface of 30 mm×30 mm×3 mm as a test piece, and place it in a constant temperature and humidity bath at 60°C with a relative humidity of 95% for 96 hours. Observe the polished surface with a 50-fold microscope to observe the discoloration state. The criterion is to observe the sample at 1500 lux with illuminance for 96 hours after no discoloration is found at level 1, and when observed at 100 lux, the discoloration is not found but can be detected at 1500 lux as level 2 , Set the person who can be found to be discolored when observed at 100 lux as level 3. In addition, for level 3, after re-placement in a constant temperature and humidity chamber at 50°C with a relative humidity of 85% for 6 hours, observe the polished surface with a 50-fold microscope, and set the color change that can be found by 1500 lux as level 4. If no discoloration is found, it will still be considered as level 3. The transmittance of the glass of the Examples and Comparative Examples was measured according to the standard JOGIS02 of the Optical Glass Industry Association of Japan. Furthermore, in the present invention, by measuring the transmittance of the glass, the presence or absence and degree of coloration of the glass are determined. Specifically, the opposing parallel polished product with a thickness of 10±0.1 mm is measured in accordance with JISZ8722, and the spectral transmittance of 200 to 800 nm is measured, and λ 5 (wavelength when the transmittance is 5%) and λ 80 (when the transmittance is 80%) are determined.的wavelength). The liquidus temperature of the Examples and Comparative Examples was obtained by placing the crushed glass samples on a platinum plate at 10 mm intervals, keeping them in a furnace with a temperature gradient of 800°C to 1200°C for 30 minutes, and then taking them out. After cooling, use a microscope with a magnification of 80 times to observe the presence or absence of crystals in the glass sample for measurement. At this time, the optical glass was pulverized into particles with a diameter of about 2 mm as a sample. [Table 1] [Table 2] [table 3] [Table 4] [table 5] [Table 6] [Table 7] [Table 8] [Table 9] [Table 10] [Table 11] [Table 12] As shown in the tables, the partial dispersion ratio (θg, F) and Abbe number (ν d ) of the optical glass of the embodiment of the present invention satisfy (-0.00256×ν d +0.637)≦(θg,F)≦ The relationship of (-0.00256×ν d +0.684), more specifically, satisfies the relationship of (-0.00256×ν d +0.657)≦(θg, F)≦(-0.00256×ν d +0.679). In particular, the optical glass of the embodiment (No.B1~No.B52, No.C1~C3) satisfies (-0.00256×ν d +0.657)≦(θg,F)≦(-0.00256×ν d +0.677 ) Relationship. Here, the relationship between the partial dispersion ratio (θg, F) and Abbe number (ν d ) of the glass in the examples of the present case is shown in FIG. 2. The refractive index (n d ) of the optical glass of the embodiment of the present invention is 1.60 or more, more specifically, it is 1.65 or more, and the refractive index (n d ) is 1.78 or less, more specifically, it is 1.76 or less. Need to be within range. In particular, the refractive index (n d ) of the optical glass of the examples (No. A1 to No. A28, No. C1 to C3) is 1.75 or less, and more specifically, it is 1.73 or less. In addition, the Abbe number (ν d ) of the optical glass of the embodiment of the present invention is 28 or more, more specifically, 30 or more, which is within the required range. In addition, the Abbe number (ν d ) of the optical glass of the example of the present invention is 47 or less, more specifically, 46 or less, which is within a desired range. In particular, the Abbe number (ν d ) of the optical glass of the examples (No. A1 to No. A28, No. C1 to C3) is 43 or less. In addition, the λ 80 (wavelength at a transmittance of 80%) of the optical glass of the embodiment of the present invention is 420 nm or less, more specifically, 400 nm or less. In particular, the λ 80 (wavelength at 80% transmittance) of the optical glass of the examples (No. A1 to No. A28, No. C1 to C3) is 390 nm or less. In addition, the λ 5 (wavelength at 5% transmittance) of the optical glass in the examples of the present invention is all 365 nm or less, more specifically, 345 nm or less, and more specifically, 340 nm or less. In particular, the λ 5 (wavelength at 5% transmittance) of the optical glass of the examples (No. A1 to No. A28, No. C1 to C3) is 335 nm or less. From this, it can be seen that the optical glass of the embodiment of the present invention has a relatively high transmittance with respect to visible light and is not easy to be colored. In addition, the liquidus temperature of the optical glass of the examples of the present invention (No.A1 to No.A28, No.C1 to C3) is 1200°C or less, more specifically, 1110°C or less, and more specifically, 1050°C the following. Therefore, these optical glasses are unlikely to cause devitrification or opalescence due to reheating, so it is presumed that they have high reheat press formability. In addition, the surface method weather resistance of the optical glass of the examples of the present invention (No. B1 to No. B52, No. C1 to C3) is level 1. Therefore, it is clearly understood that these optical glass-based surface methods are excellent in weather resistance and hardly produce so-called discoloration optical glass. Furthermore, the optical glass of the embodiment of the present invention is used to form a glass block, and the glass block is ground and polished to be processed into the shape of a lens and a rim. As a result, it can be stably processed into various lens and lens shapes. Furthermore, although the optical glass described in Comparative Example (No.b) satisfies the required optical constants (n d , ν d ), it has relatively large partial dispersion and low abnormal dispersion, and has poor transmittance, and is chemically durable. The performance is also poor, so it is impossible to obtain the refractive index (n d ) and Abbe number (ν d ) targeted by the invention in this case, and the partial dispersion ratio (θg, F) is small and the weather resistance of the surface method is small. Good optical glass. Above, the present invention has been described in detail based on the purpose of illustration, but please understand that this embodiment is always only for the purpose of illustration, and various changes can be made by the industry without departing from the spirit and scope of the present invention.