TW200937053A - Polarizer and method for making the same - Google Patents

Polarizer and method for making the same Download PDF

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Publication number
TW200937053A
TW200937053A TW97149635A TW97149635A TW200937053A TW 200937053 A TW200937053 A TW 200937053A TW 97149635 A TW97149635 A TW 97149635A TW 97149635 A TW97149635 A TW 97149635A TW 200937053 A TW200937053 A TW 200937053A
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Taiwan
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transparent substrate
polarizer
polarizing plate
adhesive layer
adhesive
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TW97149635A
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Chinese (zh)
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Atsushi Kanazawa
Hakaru Miyakita
Yumiko Hashimoto
Takashi Fujii
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Sumitomo Chemical Co
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  • Projection Apparatus (AREA)
  • Liquid Crystal (AREA)

Abstract

This invention provides a polarizer having a pair of transparent substrates corresponding to and disposed apart from each other, wherein at least one piece of polarizing element is provided in between a first transparent substrate positioned at the outermost place of one side of the polarizer, and a second transparent substrate positioned at the outermost place of another side of the polarizer. A first adhesive agent layer is provided on the side of the polarizing element and a second adhesive agent layer is provided on another side of the polarizing element: the first adhesive agent layer and the second adhesive agent layer having different glass transition temperatures.

Description

200937053 — 六、發明說明: 【發明所屬之技術領域】 本發明是有關適用於前投影機(front projector)、背 投影機(Rear Projector)等投射型液晶顯示裝置的偏振片 (偏光板’ polarizer)及其製造方法。 【先前技術】 為了對應大畫面化,取代以往的布勞恩管(Br〇wn tube) ❹i .4示裝置’投射型液晶顯示裝置快速地在業務用途以及 豕庭用途中普及。在此,投射型是指,將光源發出的光分 離成KGB三原色之後,使各色光在各自的光路中通過液晶 面板、偏振片等,最終通過投射透鏡擴大,在螢幕上成像 ==圖像的方式。對於投射型液晶顯示裝置,從觀察者 衆欲看時將圖像投射於螢幕仙的前投影機主要是用於 ^務’而將圖像投射於内側的背投影機主要是用於家 展,晶顯示震置近年來畫面的高亮度化得到, 用。因此,對L放出強力光的高壓水銀燈被作為光㈣ 過該配置的偏振片要求:即使長咖 濕下長期保存=生7^漏的_耐光性,以及,在^ 時將兩者合併簡記為不會:先生^^^ 光性=決定投射型液晶顯示裝置壽:=片- 方案::如在開平10-39138 第1圖所示,將熱傳導率高的玻螭等透明 320867 3 <4 200937053 基板1、2通過相同的接著劑層4安裝在偏振器(偏光子)3 , 的兩面’使偏振β 3產生的熱傳導到透明基板卜2,從❿ · ㈣部釋㈣㈣C例如參照[實施例卜⑽⑻至⑽灿。. 【發明内容】 現在’在投射型液晶顯示裝置中要求增加光源的光強 度。在這樣的情況下,對偏振片的耐光性和耐熱性方面要 求更進-步提高。因此,本發明的目的在於提供财光性和 耐熱性非常優異的、能夠小型化之前投影機、背投影機# 投射型液晶裝置的光學系統之偏振片,具有該偏振片的光0 學構件、投射型液晶顯示|置以及偏振片的製造方法。 本發明提供-種偏振片’其是至少兩片透明基板為相 對隔離著,在位於-方最外側的第i透明基板與位於另一 方最外侧的第2透明基板之間,設有至少一片偏振器其 中’在偏振器的-面侧設有第i接著劑層,在另一面侧設 有=2接著劑層,第i接著劑層與第2接著劑層的破璃移 轉/JDL度不同。這種偏振片的耐光性和耐熱性非常優異,還 ❹ 能夠小型化前投影機、背投影機等投射型液晶裝置^光學 系統。 在上述偏振片中,在第1接著劑層和第2接著劑層中, 如果一方接著劑層由彈性接著劑或膠黏劑形成、另一方接 著劑層由固化性接著劑形成時,則能夠更進一步提高耐熱 性。 ’ 對於本發明的偏振片來說,在第1透明基板與第2透 明基板之間設置一片偏振器,以偏振器經由第丨接著劑層 320867 4 200937053 - 而與第1透明基板接合,姆λ贫。# 夜 左由第2接著劑層而與第2透明 基板接合為佳。 本發明的偏振片,也可以採用如下形態:在第上透明 基板與第2透明基板相對的内面,分別形成第^接著劑層, 藉由第1接㈣層’在上述各透縣板上安裝相互不同的 兩片偏振器。 、在上述偏振片中,以第2接著劑層接合:安裝於第1 〇透明基板上的偏振器的與第i接著劑層相接的面的相反侧 的面、和安裝於第2透明基板上的偏振器的與第1接著劑 層相接的面的相反側的面為佳。 分別安裝於第1透明基板與第2透明基板上的偏振器 的、與第1接著劑層相接的面的相反侧的面上分別形成保 護層,保護層之間以使用第2接著劑層接合為宜。 上述偏振片中’分別安裝於第1透明基板與第2透明 基板上的偏振器的’與第1接著劑層相接的面的相反側的 ❹面上’分別形成保護層,保護層之間以夾著第3透明基板 而用第2接著劑層接合為宜。 在本發明的偏振片中,於中,心波長為44 Οηπι、5 5 Οηπι或 610nm的光中,分別安装於第1遂明基板與第2透明基板 上的偏振器中的一方偏振器的吸收轴方向的透過率以10% 至70%,另一方偏振器的吸收軸方向的透過率以1%以下 為佳。使偏振器的透過率在上述範圍内,可以抑制偏振片 的劣化。 上述偏振器的水分含量為5重量%以下時,可以大幅 320867 200937053 提局偏振片的财光性。 在本發明的偏振片中,如果上述偏振器在聚乙烯醇系 樹脂的偏振器基板上吸附配向有二色性染料或碘的偏振器, 或者上述偏振器是由聚乙烯醇/聚乙烯基嵌段共聚物所成 的膜時,則可以更進一步提高耐光性。 從提高偏振片之耐光性的觀點而言,第1透明基板和 第2透明基板中的至少一方之熱傳導率以5W/(m · K)以上 為佳。 從進一步提高偏振片的耐光性的觀點而言,第1透明 基板和第2透明基板中的一方之材質是選自由水晶、藍寶 石、氧化鎂和尖晶石所成群組中的至少一種,另一方的材 質是選自由氧化鎂、尖晶石、石英玻璃、矽酸鹽玻璃、硼 矽酸鹽玻璃和水晶所成群組中的至少一種為佳。 第1透明基板和第2透明基板中的至少一方是單晶的 透明基板時,偏振片的耐光性變得更加優異。 本發明還提供將上述本發明的偏振片和相位差膜接合 而成的光學構件。 本發明還提供上述偏振片的製造方法,其具有在減壓 下形成第1接著劑層和/或第2接著劑層的步驟。 在上述偏振片的製造方法中,以復具有在130°C以下 的溫度乾燥安裝於透明基板的偏振器的步驟為佳。由此, 可以適當地調整偏振器的水分量。 本發明還提供具有上述偏振片和液晶顯示面板的投射 型液晶顯示裝置。這樣的投射型液晶顯示裝置,由於具有 6 320867 200937053 _ 本發明的偏振片,因此能夠充分小型化光學系統。 在上述投射型液晶顯示裝置中,以第1透明基板和第 2透明基板中的至少一方是單晶的透明基板,該單晶的透 明基板以成為液晶顯示面板側的方式設置上述偏振片為 佳。 本發明的偏振片,初期财光性、長期耐光性和财熱十生 都優異。 【實施方式】 (發明實施之最佳形態) 以下,對於本發明的偏振片以及使用其的投射型液晶 顯示裝置,對應需要邊參照附圖,邊對本發明的適合實施 方式進行詳細說明,但本發明並不侷限於這些實施方式。 同時,附圖中,相同要素標以相同符號,並省略重復說明。 此外,上下左右的位置關係只要沒有特別說明,就是根據 附圖所示的位置關係。進而,附圖的尺寸比率並不侷限於 ❹圖示的比例。 第1圖_是表不本發明相關偏振片的一種實施方式的概 要圖。_第1圖的偏振片I,係在偏振器3的一面’經由接著 劑層(第1接著劑層)4接合透明基板(第1透明基板)1,在 偏振器3的另一面,經由接著劑層(第2接著劑層)5接合 透明基板(第2透明基板)2。接著劑層4與接著劑層5的玻 璃移轉溫度不同。即使由於強力光透過時產生的熱而在偏 振片内部產生應力變形,藉由在偏振器3的兩面形成的、 玻璃移轉溫度不同的接著劑層4和接著劑層5,也能夠吸 7 320867 200937053 收緩=應力變形,可有效地抑制偏振器3剝離等不良情 兄形成接著劑層4、5的接著劑,以顯示有黏合性 々接著劑(所π的膠黏劑)為宜。此外,本發明的接著劑層 通常是透明的。 接著劑層4、 、w 、 、5的玻璃移轉溫度只要不同即可,對具體 =皿,沒有特别限定’但以接著劑層的玻璃移轉溫度的差 為60 C以上為# 0 轉溫度為曹c至推薦:使一方的接著劑層的玻璃移 〜怠、1() c,更佳為-7(TC至-3(TC之範圍,使 炎0Λ方的接著剩層的玻璃移轉溫度為50°C至20(TC,更佳 為 80C 至 •堂λ· _所測定的值-。其中’玻璃移轉溫度是根據順 接著移轉溫度為_8代至-阶的接著劑層的 如:彈性接—時5己為“接著劑A”)的具體例,可以列舉 (例如丙缔酸橡膠、丙稀酸類橡膠)以及膠黏劑 〇 接著麵移轉溫度為抓至_°C的接著劑層的 如:環氧椒Λ時記為“接著劑B”)的具體例,可以列舉 環氧樹月旨ΕΡΘ582接著劑(例如Cemedine公司製的熱固化性 κ_5Α)、聚^舰KA公司製的紫外固化性環氧樹脂 性接著劑·石夕蓋二樹脂系接著劑、紛樹脂系接著劑等熱固化 甲聚_&質^ (例如紫外線固化型錢基末端具有 等紫外線固化‘:::)。、氰基丙烯酸醋、丙烯酸類樹脂 作為在本發明使用的透明基板卜2的材質,可以列舉 320867 8 200937053 如無機透明材料。具體而言,可例示如:石夕酸鹽玻璃、哪 砍酸鹽玻璃、鈦矽酸鹽玻璃、熔融石英(石英玻璃)、水晶、 藍寶石、YAG結晶、熒石、氧化鎂、尖晶石(Mg〇 · Al2〇3)。 其中’從將偏振器3產生的熱有效率地釋放到外部,將偏 振器3低溫化而提高偏振片的耐光性的觀點而言,熱傳導 率以在5W/mK以上的材質為佳。作為這樣的材質,可以列 舉如:水晶或藍寶石、氧化鎂、尖晶石。此外,透明基板 θ 1、2中的至少一方以單晶為佳。作為單晶’例示有水晶、 藍寶石、YAG結晶、榮石,特别以水晶、藍寶石為佳。. 此外,透明基板1、2中的至少一方在380nm至780nm 波長範圍中的正面相位差以小於5nm為佳。透明基板的正 面相位差小於5nm時,光源發出的光通過偏振器而產生的 偏振光的面因為沒有歪斜地通過透明基板,因此從投影機 投射的畫面之對比度變良好。作為這樣的透明基板者,可 例示如:矽酸鹽玻璃、硼矽酸鹽玻璃、欽矽酸鹽玻璃、溶 ❹融石英(石英玻璃)、氧化鎂、尖晶石。 作為具體組合,以透明基板1、2中的一方,為熱傳導 性南的氧化鎮、藍寶石、尖晶石、水晶’另.一方是正面相 位差低的氧化鎂、尖晶石、矽酸鹽破璃、硼梦酸鹽玻璃、 鈦矽酸鹽玻璃、熔融石英(石英玻璃)為佳。此外,從控制 價格較低的觀點而言’在透明基板1、2中的一方使用水 晶、矽酸鹽玻璃、硼矽酸鹽玻璃、鈦矽酸鹽玻璃、熔融石 英(石英玻璃)的構成也是有效的。 其中“正面相位差”是指,以透明基板面内的折射率 9 320867 200937053 為最大的方向作為x軸,以與χ軸垂直的方向作為γ轴, . 以透明基板的厚度方向作為ζ軸’以各個轴方向的折射率 - 為 nxl、Hyl、Πζΐ, 以膜厚為di(nm)時,用(nxl_nyl)xdi計算出 _ 的數值。 作為透明基板1、2的厚度,從工業化時的收率、與適 用的投影機光學系統的大小匹配的觀點而言,以〇· 〇5mm至 3mm為佳,更佳是〇. 賴至2mm。透明基板的厚度為〇. 〇5丽 以上時,加工時透明基板的破損得到抑制,可以穩定地製 造。此外,透明基板的厚度為3mm以下時,能夠將所得到 〇 的偏振片小型化、輕量化。 對透明基板1、2的與空氣接觸的外面,期望實施與所 使用的光之波長相對應的防止反射處理。作為防止反射處 理者,可以列舉如利用濺射法或真空蒸鍍法形成介電體多 層膜、藉由塗布賦予一層以上的低折射率層的方法。進而, 還可以對防止反射面實施為了防止表面附著污垢的防污處 理。作為防污處理,可以列舉如在表面形成對防止反射性 能幾乎沒有影響的含氟的薄臈層。 ϋ 作為本發明中使用的偏振器3者,可以列舉如:在聚 乙烯酵系的樹脂、聚乙酸乙烯酯樹脂、乙烯/乙酸乙烯酯 (EVA)樹脂、聚醯胺樹脂、聚酯樹脂等偏振器基材中吸附配 向有二色性染料或碘的物質,分子配向的聚乙烯醇膜中含 有聚乙烯醇的二色性脫水產物(聚乙烯)之配向分子鏈的聚 乙烯醇/聚乙烯嵌段共聚物。作為偏振器者,特別以在聚乙 烯醇系樹脂中吸附配向有二色性染料或碘的偏振器為佳。 320867 10 200937053 ’其中,在偏振器的基材上所用的聚乙烯醇系樹脂包 括:係作為聚乙酸乙烯酯的部分或完全皂化物的聚乙烯 醇;皂化EVA樹脂等之乙酸乙烯酯與其它能夠共聚合的單 體(例如乙烯或丙烯的烯烴類,巴豆酸或丙烯酸、甲基丙烯 酸、馬來酸的不飽和羧酸類,不飽和磺酸類,乙烯基醚類) 的共聚物之皂化物;用醛將聚乙烯醇改質而得的聚乙烯縮 甲醛或聚乙烯縮乙醛等。作為偏振器的基材者,從染料的 吸附性和配向性的觀點而言,以使用聚乙烯醇系的樹脂 @ 膜,特別是由聚乙烯醇所成之膜為佳。 由聚乙烯醇/聚乙烯嵌段共聚物所成的偏振器是指,將 經由拉伸等而分子配向的聚乙烯醇膜暴露於濃鹽酸或濃硫 酸等之中,使一部分脫水而生成聚乙烯的共軛嵌段的物 質。也可以將該共聚物直接作為偏振器,但通常將含浸有 硼酸和/或硼砂的物質作為偏振器使用。 作為偏振器的基材中吸附配向的物質者,例如以二色 ❹性染料為佳。經由使用波長依賴性不同的染料,製作各種 投射型液晶顯示裝置的藍色光路(Blue Channel)用途、綠 色光路用途、紅色光路用途的各種偏振器。 作為二色性染料者,可以列舉如在“液晶顯示裝置用 二色性色素的開發”(栢根等、住友化學、2002-11、23至 30頁)中記載的化合物。作為二色性染料者,具體可列舉 如:游離酸形態的下述通式(I)表示的化合物。 11 320867 200937053 Α^ΝBACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polarizing plate (polarizing plate 'or polarizer') for a projection type liquid crystal display device such as a front projector or a rear projector. And its manufacturing method. [Prior Art] In order to cope with a large screen, a conventional Brohn tube 投射i.4 display device liquid crystal display device has been rapidly popularized for business use and use in the court. Here, the projection type means that after the light emitted from the light source is separated into the three primary colors of KGB, the respective color lights are passed through the liquid crystal panel, the polarizing plate, or the like in the respective optical paths, and finally expanded by the projection lens to form an image on the screen == image. the way. For the projection type liquid crystal display device, the front projector that projects the image onto the screen when viewed by the viewer is mainly used for the work, and the rear projector that projects the image on the inside is mainly used for the home exhibition. The crystal display has been used in recent years to increase the brightness of the screen. Therefore, a high-pressure mercury lamp that emits strong light to L is required as a light (4) polarizer for this configuration: even if it is long-term storage under long-term wetness, it is _light-resistant, and the combination of the two is abbreviated as No: Mr. ^^^ Lightness = Decision projection liquid crystal display device life: = film - Solution: As shown in Fig. 1 of Kaiping 10-39138, the glass with high thermal conductivity is transparent 320867 3 <4 200937053 The substrates 1 and 2 are mounted on the polarizer (polarizer) 3 by the same adhesive layer 4, and the heat generated by the polarization β 3 is transmitted to the transparent substrate 2, from the 四 · (4) part (4) (4) C, for example, refer to [Example Bu (10) (8) to (10) Can. SUMMARY OF THE INVENTION Nowadays, it is required to increase the light intensity of a light source in a projection type liquid crystal display device. In such a case, the light resistance and heat resistance of the polarizing plate are required to be further improved. Therefore, an object of the present invention is to provide a polarizing plate which is excellent in both optical properties and heat resistance and which is capable of miniaturizing an optical system of a projector, a rear projector #, and a projection type liquid crystal device, and an optical member having the polarizing plate, Projection type liquid crystal display | and a method of manufacturing a polarizing plate. The present invention provides a polarizing plate which is at least two transparent substrates which are relatively isolated, and at least one polarization is provided between the ith transparent substrate located at the outermost side of the square and the second transparent substrate located at the outermost side of the other side. Wherein 'the i-th adhesive layer is provided on the side of the polarizer, and the second adhesive layer is provided on the other side, and the glass transition/JDL degree of the i-th adhesive layer and the second adhesive layer are different. . Such a polarizing plate is excellent in light resistance and heat resistance, and it is also possible to miniaturize a projection type liquid crystal device such as a front projector or a rear projector. In the polarizing plate, when one of the first adhesive layer and the second adhesive layer is formed of an elastic adhesive or an adhesive, and the other adhesive layer is formed of a curable adhesive, Further improve heat resistance. For the polarizing plate of the present invention, a polarizer is provided between the first transparent substrate and the second transparent substrate, and the polarizer is bonded to the first transparent substrate via the second adhesive layer 320867 4 200937053 - poor. #夜 Left is preferably joined to the second transparent substrate by the second adhesive layer. In the polarizing plate of the present invention, a second adhesive layer may be formed on the inner surface of the upper transparent substrate and the second transparent substrate, and the first (four) layer 'on each of the above-mentioned permeable boards may be mounted. Two polarizers different from each other. In the polarizing plate, a second adhesive layer is bonded to a surface of the polarizer attached to the first transparent substrate on a side opposite to a surface of the polarizer that is in contact with the ith adhesive layer, and is attached to the second transparent substrate. The surface of the upper polarizer on the opposite side to the surface in contact with the first adhesive layer is preferred. A protective layer is formed on each of the surfaces of the polarizer attached to the first transparent substrate and the second transparent substrate opposite to the surface in contact with the first adhesive layer, and a second adhesive layer is used between the protective layers. Bonding is appropriate. In the polarizing plate, a protective layer is formed between the protective layers, respectively, on the side faces of the polarizer attached to the first transparent substrate and the second transparent substrate on the opposite side of the surface in contact with the first adhesive layer. It is preferable to join the second transparent substrate with the second adhesive layer interposed therebetween. In the polarizing plate of the present invention, in the light having a center wavelength of 44 Οηπι, 5 5 Οηπι or 610 nm, absorption of one of the polarizers attached to the first substrate and the second transparent substrate The transmittance in the axial direction is 10% to 70%, and the transmittance in the absorption axis direction of the other polarizer is preferably 1% or less. When the transmittance of the polarizer is within the above range, deterioration of the polarizing plate can be suppressed. When the water content of the polarizer is 5% by weight or less, the transparency of the polarizing plate can be greatly improved by 320867 200937053. In the polarizing plate of the present invention, if the polarizer adsorbs a polarizer having a dichroic dye or iodine on a polarizer substrate of a polyvinyl alcohol resin, or the polarizer is embedded in a polyvinyl alcohol/polyethylene base When the film formed by the segment copolymer is used, the light resistance can be further improved. From the viewpoint of improving the light resistance of the polarizing plate, at least one of the first transparent substrate and the second transparent substrate preferably has a thermal conductivity of 5 W/(m·K) or more. The material of one of the first transparent substrate and the second transparent substrate is at least one selected from the group consisting of crystal, sapphire, magnesia, and spinel, from the viewpoint of further improving the light resistance of the polarizing plate. The material of one of the materials is preferably at least one selected from the group consisting of magnesium oxide, spinel, quartz glass, silicate glass, borosilicate glass, and crystal. When at least one of the first transparent substrate and the second transparent substrate is a single crystal transparent substrate, the light resistance of the polarizing plate is further improved. The present invention also provides an optical member obtained by joining the polarizing plate of the present invention and a retardation film described above. The present invention also provides a method for producing the above polarizing plate, which comprises the step of forming a first adhesive layer and/or a second adhesive layer under reduced pressure. In the above method for producing a polarizing plate, it is preferred to further dry the polarizer attached to the transparent substrate at a temperature of 130 ° C or lower. Thereby, the moisture content of the polarizer can be appropriately adjusted. The present invention also provides a projection type liquid crystal display device having the above polarizing plate and a liquid crystal display panel. Since such a projection type liquid crystal display device has the polarizing plate of the present invention, it can sufficiently reduce the size of the optical system. In the projection type liquid crystal display device, at least one of the first transparent substrate and the second transparent substrate is a single crystal transparent substrate, and the single crystal transparent substrate is preferably provided with the polarizing plate so as to be on the liquid crystal display panel side. . The polarizing plate of the present invention is excellent in initial fiscal properties, long-term light resistance, and rich heat. [Embodiment] (Best Mode for Carrying Out the Invention) Hereinafter, a polarizing plate of the present invention and a projection type liquid crystal display device using the same will be described in detail with reference to the accompanying drawings. The invention is not limited to these embodiments. In the drawings, the same elements are denoted by the same reference numerals, and the repeated description is omitted. Further, the positional relationship of the up, down, left, and right directions is based on the positional relationship shown in the drawings unless otherwise specified. Further, the dimensional ratio of the drawings is not limited to the ratio shown in the drawings. Fig. 1 is a schematic view showing an embodiment of the polarizing plate of the present invention. In the polarizing plate 1 of the first embodiment, the transparent substrate (first transparent substrate) 1 is bonded to one surface of the polarizer 3 via the adhesive layer (first adhesive layer) 4, and the other surface of the polarizer 3 is passed through The agent layer (second adhesive layer) 5 bonds the transparent substrate (second transparent substrate) 2. The glass transition temperature of the adhesive layer 4 and the adhesive layer 5 is different. Even if stress deformation occurs inside the polarizing plate due to heat generated when strong light is transmitted, the adhesive layer 4 and the adhesive layer 5 which are formed on both surfaces of the polarizer 3 and have different glass transition temperatures can absorb 7 320867. 200937053 Suspension = stress deformation, which can effectively suppress the adhesion of the polarizer 3, such as the peeling of the polarizer 3, to form an adhesive for the adhesive layer 4, 5, to exhibit an adhesive adhesive (adhesive of π). Furthermore, the adhesive layer of the present invention is generally transparent. The glass transition temperature of the layer 4, w, and 5 may be different, and the specific = dish is not particularly limited. However, the difference in glass transition temperature of the adhesive layer is 60 C or more. Recommended for Cao C: Make the glass of one of the adhesive layers shift ~ 怠, 1 () c, more preferably -7 (TC to -3 (the range of TC, so that the remaining glass of the inflammatory layer is transferred) The temperature is from 50 ° C to 20 (TC, more preferably from 80 ° C to λ λ · _ measured value - where 'glass transition temperature is based on the subsequent transfer temperature from _8 generation to - order of the adhesive layer For example, the specific example of "elastic bonding" when 5 is "adhesive A"), for example, (for example, propionic acid rubber, acrylic rubber) and adhesive 〇 〇 移 移 移 移 _ Specific examples of the adhesive layer such as "epoxypoxide" (hereinafter referred to as "adhesive B") include an epoxy resin 582 adhesive (for example, thermosetting κ_5 制 manufactured by Cemedine Co., Ltd.) UV-curable epoxy resin adhesive made by the company, heat-resistant gelatin, etc. For example, the ultraviolet curable type of the hydroxyl group terminal has a UV-curable ':::), cyanoacrylate vinegar, and an acrylic resin. As a material of the transparent substrate 2 used in the present invention, for example, 320867 8 200937053, such as an inorganic transparent material, may be mentioned. For example, it can be exemplified as: silicate powder glass, sulphate glass, titanium silicate glass, fused silica (quartz glass), crystal, sapphire, YAG crystal, fluorite, magnesia, spinel (Mg 〇·Al2〇3) where 'the thermal conductivity is 5 W/mK or more from the viewpoint of efficiently releasing the heat generated by the polarizer 3 to the outside and lowering the polarizer 3 to improve the light resistance of the polarizing plate. The material is preferably crystal, sapphire, magnesia or spinel, and at least one of the transparent substrates θ 1 and 2 is preferably a single crystal. Further, sapphire, YAG crystal, and sapphire are particularly preferably crystal or sapphire. Further, at least one of the transparent substrates 1 and 2 preferably has a front phase difference of less than 5 nm in a wavelength range of 380 nm to 780 nm. When the front surface difference of the transparent substrate is less than 5 nm, the surface of the polarized light generated by the light source passing through the polarizer passes through the transparent substrate without being skewed, so that the contrast of the screen projected from the projector becomes good. As such a transparent substrate For example, bismuth silicate glass, borosilicate glass, cinnamate glass, fused silica (quartz glass), magnesium oxide, and spinel. As a specific combination, in the transparent substrates 1, 2 One side is oxidized town, sapphire, spinel, crystal of heat conduction south. The other side is magnesium oxide, spinel, strontium silicate, borax acid glass, titanium citrate with low positive phase difference. Glass, fused silica (quartz glass) is preferred. In addition, from the viewpoint of low control price, 'the crystal, the bismuth silicate glass, the borosilicate glass, the titanium silicate glass, the fused silica (quartz glass) are also used for one of the transparent substrates 1 and 2 Effective. The "frontal phase difference" means that the direction in which the refractive index of the transparent substrate is 9 320867 200937053 is the x-axis, and the direction perpendicular to the x-axis is the γ-axis, and the thickness direction of the transparent substrate is taken as the x-axis. The refractive index in each axial direction is nxl, Hyl, Πζΐ, and when the film thickness is di (nm), the value of _ is calculated by (nxl_nyl)xdi. The thickness of the transparent substrates 1 and 2 is preferably from 5 mm to 3 mm, more preferably from 2 mm to 3 mm, from the viewpoint of the yield at the time of industrialization and the size of the applicable projector optical system. When the thickness of the transparent substrate is 〇. 5% or more, the damage of the transparent substrate during processing is suppressed, and it can be stably produced. Further, when the thickness of the transparent substrate is 3 mm or less, the obtained polarizing plate of ruthenium can be reduced in size and weight. For the outer surfaces of the transparent substrates 1 and 2 which are in contact with the air, it is desirable to carry out an anti-reflection treatment corresponding to the wavelength of the light used. As the antireflection treatment, a method of forming a dielectric multilayer film by a sputtering method or a vacuum deposition method and applying one or more low refractive index layers by coating can be mentioned. Further, it is also possible to carry out an antifouling treatment for preventing the surface from adhering to the antireflection surface. As the antifouling treatment, for example, a fluorine-containing hafnium layer having almost no influence on the antireflection property can be formed on the surface. ϋ As the polarizer 3 used in the present invention, for example, a polarization of a polyethylene-based resin, a polyvinyl acetate resin, an ethylene/vinyl acetate (EVA) resin, a polyamide resin, or a polyester resin may be mentioned. a material in which a dichroic dye or iodine is adsorbed in a substrate, and a molecularly oriented polyvinyl alcohol film contains a polyvinyl alcohol/polyethylene intercalation of a molecular chain of a disaccharide dehydration product (polyethylene) of polyvinyl alcohol. Segment copolymer. As the polarizer, a polarizer having a dichroic dye or iodine adsorbed and adsorbed in a polyvinyl alcohol-based resin is particularly preferable. 320867 10 200937053 'The polyvinyl alcohol-based resin used in the substrate of the polarizer includes: polyvinyl alcohol which is a partial or complete saponification of polyvinyl acetate; vinyl acetate such as saponified EVA resin and the like a saponified product of a copolymer of a copolymerized monomer (for example, an olefin of ethylene or propylene, a crotonic acid or an unsaturated carboxylic acid of acrylic acid, maleic acid, an unsaturated sulfonic acid, or a vinyl ether); Polyvinyl formal or polyvinyl acetal obtained by modifying aldehyde with polyvinyl alcohol. As the substrate of the polarizer, from the viewpoint of the adsorptivity and the alignment property of the dye, it is preferred to use a polyvinyl alcohol-based resin @ film, particularly a film made of polyvinyl alcohol. The polarizer formed of a polyvinyl alcohol/polyethylene block copolymer is obtained by exposing a polyvinyl alcohol film molecularly aligned by stretching or the like to concentrated hydrochloric acid or concentrated sulfuric acid to form a polyethylene. Conjugated block of matter. The copolymer may also be used directly as a polarizer, but a substance impregnated with boric acid and/or borax is usually used as a polarizer. As the substance which adsorbs the alignment in the substrate of the polarizer, for example, a dichroic dye is preferred. Various polarizers for blue channel use, green light path use, and red light path use of various projection type liquid crystal display devices are produced by using dyes having different wavelength dependence. The dichromatic dyes include those described in "Development of dichroic dyes for liquid crystal display devices" (Baigen et al., Sumitomo Chemical, 2002-11, pages 23 to 30). Specific examples of the dichroic dye include compounds represented by the following formula (I) in the form of a free acid. 11 320867 200937053 Α^Ν

其中,在式(I)中,Me表示選自銅原子、鎳原子、鋅原子 和鐵原子所成群組中的金屬原子。Αι表示可以被取代的苯 基或可以被取代的萘基。B1表示可以被取代的萘基,結合 於Me的氧原子和以-N=N-表示的偶氮基鍵合者是於苯環上 的位於相互鄰接位置的碳。R1和R2是各自独立,表示碳原 子數為1至4的烷基、碳原子數1至4的烷氧基、羧基、 〇 磺酸基(sulfo group)、確醯胺基(sulfon amide)、磺烧基 醯胺基(sulfonalkyl amide)、氨基、酿基氨基、墙基或鹵 素原子。 此外,作為二色性染料者,可列舉以游離酸形態的下 述通式(II)表示的化合物。Here, in the formula (I), Me represents a metal atom selected from the group consisting of a copper atom, a nickel atom, a zinc atom and an iron atom. Αι denotes a phenyl group which may be substituted or a naphthyl group which may be substituted. B1 represents a naphthyl group which may be substituted, and an oxygen atom bonded to Me and an azo bond represented by -N=N- are carbons located adjacent to each other on the benzene ring. R1 and R2 are each independently and represent an alkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a carboxyl group, a sulfo group, a sulfonamide, or the like. Sulfonyl amide, amino, arylamino, wall or halogen atom. Further, examples of the dichroic dye include compounds represented by the following formula (II) in the form of a free acid.

R4 0HR4 0H

其中,在式(II)中,A3和B3是各自獨立,表示亦可以被取 代的苯基或亦可以被取代的萘基,R3和R4是各自獨立,表 示氫原子、碳原子數為1至4的烧基、碳原子數為1至4 的烷氧基、羧基、磺酸基、磺醯胺基、磺烷基醯胺基、氨 基、鹵素原子或石肖基,m表示0或1。 進而,作為二色性染料者’可列舉以游離酸形態的下 12 320867 200937053 述通式(III)表示的化合物。 q1-n=n-q2-x-q3-n = n-q4 (ΠΙ) 其中’在式(III)中,Q和Q是各自獨立,表示亦可以被取 代的本基或亦可以被取代的萘基,Q2和Q3是各自獨立表 示亦可以被取代的苯伸基。此外,X表示分別用下述式 (III-1)或式(III-2)表示的二價基團。 —N = N~ —N == N-1 ο (H-l) (m-2) 此外,作為二色性染料者 述通式(IV)表示的化合物。Wherein, in the formula (II), A3 and B3 are each independently, and represent a phenyl group which may also be substituted or a naphthyl group which may be substituted, and R3 and R4 are each independently, and represent a hydrogen atom and have 1 to 1 carbon atom. The alkyl group of 4, an alkoxy group having 1 to 4 carbon atoms, a carboxyl group, a sulfonic acid group, a sulfonylamino group, a sulfoalkylguanamine group, an amino group, a halogen atom or a schlossyl group, and m represents 0 or 1. Further, examples of the dichroic dye include a compound represented by the above formula (III) in the form of a free acid in the following 12 320867 200937053. Q1-n=n-q2-x-q3-n = n-q4 (ΠΙ) where 'in formula (III), Q and Q are each independently, indicating that the base may also be substituted or may be substituted Naphthyl, Q2 and Q3 are each independently represented by a phenyl extended group which may also be substituted. Further, X represents a divalent group represented by the following formula (III-1) or (III-2), respectively. —N = N~ —N == N-1 ο (H-l) (m-2) Further, as a dichroic dye, a compound represented by the formula (IV).

0~Me—0 N=N~Q' 可列舉以游離酸形態的下 (IV) 其中,在式(IV)中,Me表示選自銅原子、鎳原子、鋅原子 q和鐵原子所成群組中的金屬原子,Q5和Q6是各自獨立,表 不亦可以具有取代基的萘基,與Me結合的氧原子和以 -N-N-表示的偶氮基鍵合於苯環上的位於相互鄰接位置的 碳上。R和R6是各自獨立,表示氫原子、碳原子數為i至 4的烷基、碳原子數為丨至4的烷氧基或磺酸基。γ表示分 別用下式(IV-1)或式(iv -2)表示的二價基團。 —N = N- (l?-i) -N = N~ (IV-2)0~Me—0 N=N~Q′ may be exemplified as the lower (IV) in the form of a free acid. In the formula (IV), Me represents a group selected from a copper atom, a nickel atom, a zinc atom q, and an iron atom. The metal atoms in the group, Q5 and Q6 are each independently, and represent a naphthyl group which may have a substituent. The oxygen atom bonded to Me and the azo group represented by -NN- are bonded to each other on the benzene ring. Position on the carbon. R and R6 are each independently and represent a hydrogen atom, an alkyl group having from 1 to 4 carbon atoms, an alkoxy group having a carbon number of from 4 to 4 or a sulfonic acid group. γ represents a divalent group represented by the following formula (IV-1) or formula (iv-2), respectively. —N = N- (l?-i) -N = N~ (IV-2)

I Ο 13 320867 200937053 此外,作為二色性染料者,可列舉由C. I.直接黃12、 C. I.直接紅31、C. I.直接紅28、C. I.直接黃44、C. I.直 接黃28、C. I.直接橙107、C. I.直接紅79、C. I.直接紅2、 C. I.直接紅81、C. I.直接橙26、C. I.直接橙39、C. I.直 接紅247以及C. I.直接黃142所成群組所示的用染料索引 通用名(Color Index Generic Name)表示的物質。 二色性染料亦可以以游離酸的形態使用,還可以以銨 鹽、乙醇胺鹽、烷基胺鹽等胺鹽的形態使用。二色性染料 通常以鋰鹽、鈉鹽、鉀鹽等鹼金屬鹽的形態使用為佳。所 述二色性染料可以單獨使用一種或將兩種以上組合使用。 偏振器例如如下製造。首先,將二色性染料溶解於水 中,使得濃度為0.0001至10重量%左右,製備染浴。根 據需要亦可以使用染色助劑。例如,將作為染色助劑的芒 硝溶解在染浴中,使得濃度為〇. 1至10重量%為宜。 在如此調製的染浴中浸潰偏振器的基材,進行染色。 以染色溫度為40至80°C為佳。染料的配向經由將染色前 的偏振膜基材或經染色的偏振器基材拉伸來進行。作為拉 伸的方法,可以列舉如用濕式法或幹式法等進行拉伸的方 法。 為了提高偏振器的透光率、偏振度和耐光性之目的, 也可以進行硼酸處理等的後處理。硼酸處理根據所用偏振 器基材的種類或所用染料的種類而不同,通常是使用濃度 調整到1至15重量%、更佳為5至10重量%範圍的硼酸 水溶液,在30至80°C、更佳為50至80°C的溫度範圍浸潰 14 320867 200937053 偏振膜基材的處理。進而根據需要,還可以並用含有陽離 子系高分子化合物的水溶液進行固定處理。 本發明中使用的偏振器3的水分含量以5重量%以下 為佳’更佳為1重量%以下。對於在PVA中添加二色性染 料,成的偏振器,如果使水分含量為5重量%以下時,則 顯著抑制染料之分解’可以大幅提高所得偏振片的财光性。 偏振器3的水分含量的測定方法是將偏振器以曝露的 狀態在130°c通風乾燥20分鐘,求出偏振器重量的減重所 占的比例的方法。即,由下式算出偏振器的水分含量。 水分含量(%)= [(W 卜 W2)/wi]xi〇〇 W1 .偏振器乾燥前的重量,:偏振器乾燥後的重量 偏振器3的水分含量的調整係經由乾燥偏振器來進 行。用於將偏振器3的水分含量調整到5重量%以下的乾 燥步驟,可以是在偏振器3完全沒有與透明基板i、2接合 的階¥又,還可以是在偏振器3的單面或兩面接合透明基板 ❹1、2後的階段。為了能夠維持偏振器的平坦性,而且從偏 振器3的未與透明基板接合的面迅速地除去水分,以在單 面接合透明基板的階段進行乾燥為更佳。此時,還有水分 不會從乾燥後的透明基板側侵入,容易維持偏振器的乾燥 狀態的優點。此外,在偏振器3的單面接合透明基板的階 段進行乾燥’在偏振器的另一單面接合透明基板之後,在 130°C以下的溫度進行乾燥時,則能夠進一步乾燥偏振器, 因此較佳。 作為乾燥的方法’可以使用以往習知的方法可以列 320867 200937053 舉如:加熱乾燥法、減壓乾燥法。從偏振片的生產設備的 簡易性而言,以加熱乾燥法為宜。作為加熱乾燥法,可以 列舉如放入加熱烘箱的方法;對偏振片照射光,利用偏振 器吸收光而導致偏振片本身發熱的方法。作為加熱乾燥法 中的加熱溫度,與加熱方法無關,以130°C以下為佳,更 佳為40°C至130°C。經由設為40°C以上,可以在較短的時 間内結束乾燥,經由設為130°C以下,可以抑制接著劑層、 保護層的劣化以及偏振器的光學特性的劣化。 接著,對於本發明的偏振片的製造方法,以第1圖所 示的偏振片的情況作為例子進行說明。在該製造方法中, 包括:形成接著劑層4、5的步驟,以及經由接著劑層4、 5將偏振器3和透明基板1、2接合的步驟。其中重要的是 在減壓下進行接著劑層的形成。由此防止氣泡混入接著劑 層4、5。進而,利用接著劑層4、5的偏振器3與透明基 板4、5的接合也期望在減壓下進行。同時,接著劑層4、 5的形成是在偏振器3和透明基板1、2的一方或兩方形成 即可。 作為第1圖的偏振片的製造方法的具體例,例示如以 下的形態。 (1) :在偏振器3的兩面分別塗布兩種不同的接著劑而 形成接著劑層4、5之後,用接著劑層4、5接合透明基板 1、2的方法。 (2) :在透明基板1上塗布接著劑A,在得到的接著劑 層4上接合偏振器3,並在偏振器3上塗布接著劑B,在得 16 320867 200937053 到的接著劑層5上接合透明基板2的方法。 (3) :在透明基板1上塗布接著劑B,在得到的接著劑 層4上接合偏振器3,並在偏振器3上塗布接著劑A,在得 到的接著劑層5上接合透明基板2的方法。 于 (4) :在透明基板1上塗布接著劑A,在得到的接著劑 層4上接合偏振器3,另外,在透明基板2上塗布接著劑/, 將得到的接著劑層5和偏振器3接合的方法。 ❹ (5):在透明基板1上塗布接著劑β,在得到的接著劑 層4上接合偏振器3’另外,在透明基板2上塗布接著劑心 將得到的接著劑層5與偏振器3接合的方法。 (6) :在偏振器3上塗布接著劑A,在得到的接著劑層 4上接合透明基板〗’並在偏振器3上塗布接著劑β,在^ 到的接著劑層5上接合透明基板2的方法。 (7) .在偏振器3上塗布接著劑β,在得到的接著劑層 4上接合透明基板1,並在偏振器3上塗布接著劑a,在得 Ο 到的接著劑層5上接合透明基板2的方法。 (8) :在偏振器3的單面塗布接著劑a形成接著劑層5, 另外’在透明基板1上塗布接著劑β,在得到的接著劑層4 上接合偏振益3的沒有塗布接著劑Α.的面,並在接著气居 5上接合透明基板2的方法《>. (9) :在偏振器3的單面塗布接著劑Β形成接著劑層5, 另外’在透明基板1上塗布接著劑A,在得到的接著劑層4 上接合偏振器3的沒有塗布接著劑,的面,並在接著^層 5上接合透明基板2的方法。 β胃 320867 17 200937053 f發明的偏振片的其它實施形態示於第2圖至 圖。廷些圖所示的偏振片與第i圖的偏振片的不同點在 於’偏振11 3的、*與接著劑層4、5接觸的露出部分 ㈣7被覆。由此’防止水分從空氣中侵人 偽 振器3的耐熱性提高。 器3偏 在第2圖的偏振片中,偏振器3的、不與接著劑層4、 5接觸的露出部分職封劑7覆蓋。此外,接著劑層㈠ ,同時用密封劑7覆蓋。該密封劑7形成於偏振器3和接 著劑層4、5的外周部領域,例如偏振器3細邊形時形 成於其全部四個邊。第3圖的偏振片是透明基板2的面積 小於偏振器3和接著劑層4、5時的例子,位於透明基板i 與透明基板2的狹窄部的偏振器3和接著劑層4、5的外周 部被密封劑7被覆。第4圖的偏振肢透明基板卜2的面 積小於偏振器3和接著劑層4、5時的例子,從透明基板1 泮透月基板2向外突出的偏振器3和接著劑層4、5的外周 部被密封劑7被覆。 作為密封劑7者,可以使用以往習知的密封劑,在加 工時具有流動性,加工後固化而具有密封功能的物質因而 為佳。例如,可以適合使用紫外線固化型樹脂、熱固化型 樹脂’或者由兩者的作用而固化的樹脂。使用加工時具有 流動性的樹脂時,該樹脂固化前的黏度以lOOPa· s以下為 佳’更佳是〇.〇lPa · s至50Pa · s的範圍。 能夠在本發明中使用的密封劑7,亦可以是與形成上 述接著劑層的接著劑A或B相同種類的物質。作為密封劑 18 320867 200937053 •者,具體例示乙稀-酸軒共聚物(例如杜邦· 標“眶等聚歸煙系樹脂、環氧樹脂系接著劑=商 cemedine公司製的熱固化性環氧樹脂、商品名 如 ADEKA公司製的紫外固化性環氧樹脂、商品名“狀哪A” Three bond公司製的紫外固化性環氧樹脂、商品’ “TB3025G” ’NagaseCheratex&5l 製的紫外固化性匕、 商品名“XNR5516Z”)、聚氨酯樹脂系接㈣、_ ^曰、 ❹著劑等熱固化性接著劑;石夕氧_例如紫外線固= 乳烧、具有甲魏基末端聚㈣的改質錢燒樹脂) 而 婦酸酯、丙烯酸類樹脂等紫外線固化性接著劑。 使用固化性樹脂作為密封劑7時,固化前的揮發八 以在2重量%以下為佳,更佳為j重量%以下者。如: 揮發成分為2重量%以下的密封劑時,則可抑制加= 密封劑内產生微小氣泡,並且能夠在減壓下進行密封劑的 塗布’加工收率大幅提高。在此,揮發成分是根據‘‘了 ❹ 6249”所測定得到的值。 ^ 此外,密封劑7固化後的玻璃移轉溫度以在耽以 上,煮沸吸水率以在4重量%以下為佳。由此可以提 熱性,並且水分從大氣向驗器的侵人得到抑制,偏 的财光性提高。其中’煮沸吸水率是指,將密封劑的固化 物在彿水巾韻1小時後增加的#量,相對於浸潰前的固 化物質量的百分率,係根據“JIS κ 6911,,求出的。 密封劑7的透濕度通常是以6〇g/(m2.24hr)以下為佳, 更佳為25g/m2.24hr以下。密封劑的透濕度為6〇g/m2.24hr 19 320867 200937053 以下時,能夠進一步抑制水分從大氣向偏振器的侵入,能 夠提向偏振片的耐光性。在此’透濕度是指,根據“jISZ 0208”求出將密封劑調整成為厚度1〇〇/zm的固化物在溫 度40°C、相對濕度90%的環境下透過的水分量。 接者,對於偏振片具有2片偏振器時的實施形態進行 說明。在第5圖中表示具有2片偏振器的偏振片的實施形 態的例子。第5圖的偏振片,在相對隔離的2片透明基板 卜2的相對内面,分別形成接著劑層4a、4b,經由這些接 著劑層4a、4b在透明基板1、2上分別安裝2片偏振器 3b。接著,以接著劑層6接合偏振器3a、3b的與接著劑層 4a、4b相接面之相反侧的面.因此,偏振器知、北和^ 著劑層4a、4b、6的露出部分是用密封劑7覆蓋。經由如 此構成,防止水分從空氣中向偏振器3a、3b侵人而且減 輕對偏振器3a、3b的熱貪荷。 f中’接著劑層4a與接著劑層6的坡璃移轉溫度、以 及接者劑層6與接著劑層4b的玻璃移轉溫度各個不同是重 點。由此,即使是使用2片偏振器的偏振片,由於熱= 偏振片内部產生的應力變形,也被玻璃移轉不同 著劑層4a、4b、6吸收、緩和,從而有致地抑制 剝離等的不良情況。同時’具有3片以上 从 的情況也同樣地發揮本發明的作用。 1的偏振片 將偏振器3a和偏振器3b接合的接著 轉溫度以在—至-irc之範圍為佳接著更= -3(TC的範圍。此外,將偏振器3a和透 疋70 C至 处乃基板1接合的接 320867 20 200937053 者劑層4、以及將偏振器北和透明基板^接的接著劑層 5的玻璃移轉溫度以在赃至翁c的範圍為佳,更佳在 80至120°C的範圍。 玻璃移轉溫度為-8(TC至-1G。⑽接著#]和玻璃移轉溫 度為5〇°C以上的接著劑的具體例,在此例示上述的例子。 在第5圖所不的偏振片中,以使入射光8為最初透過 的偏振器3b的吸收軸方向的透過率,高於入射光8接著透 ❹過的偏振器3a的吸收軸方向的透過率為佳。具體而言,對 於所使用的光之中心波長,以使光第二透過的偏振器如吸 收軸方向的透過率為1%以下,使光最初透過的偏振器% 的吸收軸方向的透過率為10%至7〇%為佳。如果偏振器 3b的吸收軸方向的透過率小於1〇%時,則偏振器牝的發 熱量增大而恐怕會有可能促進偏振器3b的劣化。另一方 面,偏振器3b的吸收轴方向的透過率大於7〇%時,偏振 器3a的發熱量有增大的可能。經由將偏振器3b的吸收轴 ©方向的透過率設為10%至70%,偏振器3a和偏振器牝在 熱負荷方面不會產生不均,能夠抑制將偏振器如和偏振器 3b —體層疊而成的偏振片的劣作。同.時,所使用的光中心 波長是隨RGB之顏色而不同,測定吸收軸方向的透過率的 波長:Rch 為 610nm,Gch 為 550nm,Bch 為 440nm。 偏振器3a、3b的材質和製法’在此可以例示上述的例 子’對於透明基板1、2和密封劑7的材質等可以例示上述 的例子。 在第5圖所示的偏振片的製造方法中,與上述的偏振 21 320867 200937053 器為1片的偏振片的情況相同’包括形成接著劑層化、仆 6的步驟以及經由接著劑層4a、4b、6而將偏振;§如、% 和透明基板1、2接合的步驟。接著劑層4a、4b、6的形 在減壓下進行。 作為第5圖的偏振片的製造方法的具體例例示如下的 形態。 、 (1)在按照透明基板i、接著劑層4a、偏振器3a的順 序積層而成的中間體A的、偏振器3㈣沒有形成接著劑層、 4a的面(以下有時將其稱為中間體A的偏振器面)上形成接 著劑層6,並將接著劑層6與按照透明基板2、接著劑層 4b、偏振器3b的順序積層而成的中間體B的、偏振器北 的沒有形成接著劑層4b的面(以下有時將其稱為中間體B 的偏振器面)接合的方法。 (2)在中間體b的偏振器面上形成接著劑層6,並將中 間體A的偏振器面接合的方法。 (3)將中間體B的偏振器面與按照透明基板i、接著劑 層知、偏振器3a、接著劑層6的順序層叠而成的中間體c 的接著劑層6接合的方法。 ⑷將t間體A的偏振器面與按照透明基板2、接著劑 偏振器3b、接著劑層6的順序層疊而成的中間㈣ 的接者劑層6接合的方法。 層暴LI錢照偏鮮3&、接著細6、偏腳3b的順序 中間體E的、偏振器^的沒有形成接著劑層6 4接著綱4a,並將接著劑層^與透明基板i 320867 22 200937053 接合而形成中㈣卜接著,在偏㈣_ :層:的面(以下有時將其稱為中間體F的偏振器面S 成接者劑層4b,將接著㈣4b與透明基板2接合 ⑹在中間體E的偏振n 3b的沒有形成接著劑層、的 面上形成接著劑層4b,將接著劑層4b與透明基板 而形成中間體G。接著,在偏振器3a的沒有形成接著劑; 6的面(以下有時將其稱為中間體G的偏振器面)上形成二I Ο 13 320867 200937053 In addition, as a dichroic dye, it can be enumerated by CI Direct Yellow 12, CI Direct Red 31, CI Direct Red 28, CI Direct Yellow 44, CI Direct Yellow 28, CI Direct Orange 107, CI Direct Red. 79. CI Direct Red 2, CI Direct Red 81, CI Direct Orange 26, CI Direct Orange 39, CI Direct Red 247, and CI Direct Yellow 142 are represented by the Color Index Generic Name. Substance. The dichroic dye may be used in the form of a free acid or in the form of an amine salt such as an ammonium salt, an ethanolamine salt or an alkylamine salt. The dichroic dye is usually used in the form of an alkali metal salt such as a lithium salt, a sodium salt or a potassium salt. These dichroic dyes may be used alone or in combination of two or more. The polarizer is manufactured, for example, as follows. First, a dye bath is prepared by dissolving a dichroic dye in water so as to have a concentration of about 0.0001 to 10% by weight. Dyeing aids can also be used as needed. For example, the sulphate as a dyeing aid is dissolved in the dyebath so that the concentration is preferably from 1 to 10% by weight. The substrate of the polarizer was immersed in the dye bath thus prepared and dyed. The dyeing temperature is preferably 40 to 80 °C. The alignment of the dye is carried out by stretching the polarizing film substrate before dyeing or the dyed polarizer substrate. As a method of stretching, a method of stretching by a wet method or a dry method or the like can be mentioned. In order to improve the light transmittance, the degree of polarization, and the light resistance of the polarizer, post treatment such as boric acid treatment may be performed. The boric acid treatment differs depending on the kind of the polarizer substrate used or the kind of the dye used, and is usually a boric acid aqueous solution having a concentration adjusted to a range of 1 to 15% by weight, more preferably 5 to 10% by weight, at 30 to 80 ° C, More preferably, the temperature range of 50 to 80 ° C is immersed in the treatment of 14 320867 200937053 polarizing film substrate. Further, if necessary, a fixing treatment may be carried out using an aqueous solution containing a cationic polymer compound in combination. The polarizer 3 used in the present invention preferably has a moisture content of 5% by weight or less, more preferably 1% by weight or less. When a dichroic dye is added to the PVA, the polarizer having a water content of 5% by weight or less can significantly suppress the decomposition of the dye, and the gain of the obtained polarizing plate can be greatly improved. The method for measuring the moisture content of the polarizer 3 is a method in which the polarizer is ventilated and dried at 130 ° C for 20 minutes in an exposed state to determine the ratio of the weight loss of the polarizer weight. That is, the moisture content of the polarizer was calculated from the following formula. Moisture content (%) = [(W 卜 W2) / wi] xi 〇〇 W1 . Weight before polarizer drying: Weight after polarizer drying The adjustment of the moisture content of the polarizer 3 was carried out via a dry polarizer. The drying step for adjusting the moisture content of the polarizer 3 to 5% by weight or less may be a step in which the polarizer 3 is not bonded to the transparent substrates i, 2 at all, or may be one side of the polarizer 3 or The stage after bonding the transparent substrates ❹1 and 2 on both sides. In order to maintain the flatness of the polarizer and to quickly remove moisture from the surface of the polarizer 3 that is not bonded to the transparent substrate, it is more preferable to perform drying at the stage of bonding the transparent substrate on one side. At this time, there is an advantage that moisture does not intrude from the transparent substrate side after drying, and it is easy to maintain the dry state of the polarizer. Further, drying is performed at the stage of bonding the transparent substrate on one side of the polarizer 3. After the transparent substrate is bonded to the other surface of the polarizer, the polarizer can be further dried after drying at a temperature of 130 ° C or lower. good. As a method of drying, a conventionally known method can be used. For example, a heating drying method or a vacuum drying method can be used. From the viewpoint of the easiness of the production equipment of the polarizing plate, a heat drying method is preferred. As the heat drying method, for example, a method of placing in a heating oven, a method of irradiating light to a polarizing plate, and absorbing light by a polarizer to cause heat generation of the polarizing plate itself may be mentioned. The heating temperature in the heat drying method is preferably 130 ° C or less, more preferably 40 ° C to 130 ° C, irrespective of the heating method. By setting the temperature to 40 ° C or higher, the drying can be completed in a short period of time, and by setting it to 130 ° C or lower, deterioration of the adhesive layer and the protective layer and deterioration of the optical characteristics of the polarizer can be suppressed. Next, a method of producing a polarizing plate of the present invention will be described by taking the case of the polarizing plate shown in Fig. 1 as an example. The manufacturing method includes the steps of forming the adhesive layers 4, 5, and joining the polarizer 3 and the transparent substrates 1, 2 via the adhesive layers 4, 5. Of these, it is important to form the adhesive layer under reduced pressure. Thereby, air bubbles are prevented from being mixed into the adhesive layers 4, 5. Further, the bonding between the polarizer 3 of the adhesive layers 4 and 5 and the transparent substrates 4 and 5 is also desirably performed under reduced pressure. At the same time, the formation of the adhesive layers 4, 5 may be formed on one or both of the polarizer 3 and the transparent substrates 1, 2. Specific examples of the method for producing the polarizing plate of Fig. 1 are as follows. (1): A method in which two different adhesives are applied to both surfaces of the polarizer 3 to form the adhesive layers 4 and 5, and then the transparent substrates 1 and 2 are bonded by the adhesive layers 4 and 5. (2): Applying the adhesive A on the transparent substrate 1, bonding the polarizer 3 to the obtained adhesive layer 4, and applying the adhesive B on the polarizer 3 on the adhesive layer 5 of 16 320867 200937053 A method of bonding the transparent substrate 2. (3): The adhesive B is applied onto the transparent substrate 1, the polarizer 3 is bonded to the obtained adhesive layer 4, and the adhesive A is applied onto the polarizer 3, and the transparent substrate 2 is bonded to the obtained adhesive layer 5. Methods. (4): an adhesive A is applied onto the transparent substrate 1, a polarizer 3 is bonded to the obtained adhesive layer 4, and an adhesive // is applied to the transparent substrate 2, and the obtained adhesive layer 5 and polarizer are obtained. 3 bonding method. ❹ (5): The adhesive agent β is applied onto the transparent substrate 1, and the polarizer 3' is bonded to the obtained adhesive layer 4. In addition, the adhesive layer 5 and the polarizer 3 obtained by applying the adhesive core on the transparent substrate 2 are applied. The method of joining. (6): an adhesive A is applied onto the polarizer 3, a transparent substrate is bonded to the obtained adhesive layer 4, and an adhesive β is applied onto the polarizer 3 to bond the transparent substrate to the adhesive layer 5 2 method. (7) The adhesive agent β is applied onto the polarizer 3, the transparent substrate 1 is bonded to the obtained adhesive layer 4, and the adhesive a is applied onto the polarizer 3 to bond the transparent adhesive layer 5 to the bonded adhesive layer 5. The method of the substrate 2. (8): The adhesive layer 5 is applied to the one surface of the polarizer 3 to form the adhesive layer 5, and the adhesive agent β is applied on the transparent substrate 1, and the adhesive of the polarizing agent 3 is bonded to the obtained adhesive layer 4. A method of bonding the transparent substrate 2 to the surface of the gas layer 5 > (9): applying an adhesive layer on one side of the polarizer 3 to form an adhesive layer 5, and 'on the transparent substrate 1 The adhesive A is applied, and the surface of the polarizer 3 to which the adhesive is not applied is bonded to the obtained adhesive layer 4, and the transparent substrate 2 is bonded to the subsequent layer 5. β stomach 320867 17 200937053 Another embodiment of the polarizing plate of the invention is shown in Fig. 2 to Fig. The polarizing plate shown in the above figures differs from the polarizing plate in the i-th image in that the exposed portion (4) 7 of the 'polarized light 11' and the contact with the adhesive layers 4, 5 is covered. Thereby, the heat resistance of the pseudo-vibrator 3 from the intrusion of moisture from the air is prevented. The polarizer 3 is biased in the polarizing plate of Fig. 2, and the exposed portion of the polarizer 3 which is not in contact with the adhesive layers 4, 5 is covered. Further, the adhesive layer (1) is simultaneously covered with the sealant 7. The sealant 7 is formed in the outer peripheral portion of the polarizer 3 and the adhesive layers 4, 5, for example, in the shape of a thin edge of the polarizer 3, formed on all four sides thereof. The polarizing plate of Fig. 3 is an example in which the area of the transparent substrate 2 is smaller than that of the polarizer 3 and the adhesive layers 4, 5, and the polarizer 3 and the adhesive layers 4, 5 located in the narrow portion of the transparent substrate i and the transparent substrate 2 are The outer peripheral portion is covered with the sealant 7. The polarizer transparent substrate 2 of FIG. 4 is smaller than the polarizer 3 and the adhesive layers 4, 5, and the polarizer 3 and the adhesive layers 4, 5 projecting outward from the transparent substrate 1 through the moon substrate 2. The outer peripheral portion is covered with the sealant 7. As the sealant 7, a conventionally known sealant can be used, and it is preferable to have a fluidity at the time of processing and to have a sealing function after curing. For example, a resin which is cured by using an ultraviolet curable resin, a thermosetting resin, or both can be suitably used. When a resin having fluidity during processing is used, the viscosity of the resin before curing is preferably 100 Pa·s or less, more preferably in the range of 〇.1Pa·s to 50 Pa·s. The sealant 7 which can be used in the present invention may be the same type as the adhesive A or B which forms the above-mentioned adhesive layer. As a sealant, 18 320867 200937053, specifically, an ethylene-acid ruthenium copolymer (for example, DuPont· 眶 眶 聚 聚 聚 烟 烟 、 环氧树脂 环氧树脂 环氧树脂 环氧树脂 环氧树脂 环氧树脂 环氧树脂 ce ce ce ce ce ce ce ce ce ce ce ce ce The product name is UV-curable epoxy resin manufactured by ADEKA Co., Ltd., and the product name "Ana-A" is a UV-curable epoxy resin manufactured by Three Bond Co., Ltd., and the product "TB3025G" is UV-curable by "NagaseCheratex & 5l." Product name "XNR5516Z"), polyurethane resin-bonded (4), _ ^ 曰, enameling agent and other thermosetting adhesive; Shi Xi oxygen _ such as UV solid = milk burning, with a Weiwei terminal poly (four) modified money burning In the case of using the curable resin as the sealant 7, the volatilization before curing is preferably 2% by weight or less, more preferably j% by weight or less. For example, when the volatile component is 2% by weight or less of the sealant, it is possible to suppress the occurrence of fine bubbles in the sealant and the application of the sealant under reduced pressure, and the processing yield is greatly improved. The hair component is a value measured according to ‘‘了 ❹ 6249’. Further, the glass transition temperature after the curing of the sealant 7 is above 耽, and the boiling water absorption rate is preferably 4% by weight or less. As a result, heat can be extracted, and moisture intrusion from the atmosphere to the detector can be suppressed, and the partiality of the light is improved. The 'boiling water absorption rate' is the amount of the amount of the cured product of the sealant which is increased after 1 hour in the water of the water, and the percentage of the mass of the cured product before the impregnation is determined according to "JIS κ 6911". The moisture permeability of the sealant 7 is usually 6 〇 g / (m 2.24 hr) or less, more preferably 25 g / m 2.24 hr or less. The moisture permeability of the sealant is 6 〇 g / m 2.24 hr 19 320867 200937053 or less In this case, it is possible to further suppress the intrusion of moisture from the atmosphere into the polarizer, and it is possible to improve the light resistance of the polarizing plate. Here, the 'transmission humidity is obtained by adjusting the sealant to a thickness of 1 〇〇/zm according to "jISZ 0208". The moisture content of the cured product transmitted in an environment of a temperature of 40 ° C and a relative humidity of 90%. An embodiment in which the polarizing plate has two polarizers will be described. In Fig. 5, a polarizer having two polarizers is shown. An example of the embodiment of the polarizing plate. The polarizing plate of Fig. 5 forms the adhesive layers 4a and 4b on the opposite inner faces of the two transparent substrates 2, and the transparent substrate 1 is formed via the adhesive layers 4a and 4b. And 2 pieces of polarizer 3b are respectively installed on 2, and then, followed by The layer 6 joins the faces of the polarizers 3a, 3b on the opposite side of the surface where the adhesive layers 4a, 4b meet. Therefore, the exposed portions of the polarizer, the north and the coating layers 4a, 4b, 6 are made of a sealant 7 By this configuration, moisture is prevented from invading from the air to the polarizers 3a, 3b and the heat load on the polarizers 3a, 3b is alleviated. The glass transition temperature of the adhesive layer 4a and the adhesive layer 6 in f And the difference in glass transition temperature between the carrier layer 6 and the adhesive layer 4b is important. Thus, even a polarizing plate using two polarizers is subjected to heat due to stress deformation generated inside the polarizing plate. When the different agent layers 4a, 4b, and 6 are transferred and absorbed, the defects such as peeling are suppressed, and the effect of the present invention is similarly exhibited in the case of having three or more sheets. The subsequent rotation temperature of the bonding of 3a and the polarizer 3b is preferably in the range of - to -irc and then more = -3 (the range of TC. Further, the polarizer 3a and the substrate 70 are bonded to the substrate 1 at the junction of the substrate 3 20 200937053 The agent layer 4, and the polarizer north and the transparent substrate The glass transition temperature of the coating layer 5 is preferably in the range of 赃 to 翁c, more preferably in the range of 80 to 120 ° C. The glass transition temperature is -8 (TC to -1 G. (10) then #] and glass The above-described example is exemplified as a specific example of the adhesive having a transition temperature of 5 〇 ° C or higher. In the polarizing plate of Fig. 5, the incident light 8 is the absorption axis direction of the polarizer 3b that is initially transmitted. The transmittance is higher than that of the incident light 8 and then the direction of the absorption axis of the polarizer 3a that has passed through. Specifically, for the center wavelength of the light used, the polarizer that transmits the second light is The transmittance in the absorption axis direction is preferably 1% or less, and the transmittance in the absorption axis direction of the polarizer % through which light is first transmitted is preferably 10% to 7% by weight. When the transmittance of the polarizer 3b in the absorption axis direction is less than 1%, the heat generation amount of the polarizer 增大 is increased and there is a fear that the deterioration of the polarizer 3b may be promoted. On the other hand, when the transmittance of the polarizer 3b in the absorption axis direction is more than 7〇%, the amount of heat generated by the polarizer 3a may increase. By setting the transmittance in the absorption axis direction of the polarizer 3b to 10% to 70%, the polarizer 3a and the polarizer 不会 do not cause unevenness in heat load, and it is possible to suppress the polarizer such as the polarizer 3b from being formed. The inferiority of the laminated polarizers. In the same manner, the wavelength of the light center used is different depending on the color of RGB, and the wavelength of the transmittance in the absorption axis direction is measured: Rch is 610 nm, Gch is 550 nm, and Bch is 440 nm. The material and the manufacturing method of the polarizers 3a and 3b can be exemplified as the above-described examples. The above-described examples can be exemplified for the materials of the transparent substrates 1 and 2 and the sealant 7. In the method for producing a polarizing plate shown in Fig. 5, the same as the case where the polarizing plate of the above-mentioned polarizing 21 320867 200937053 is the same, 'including the step of forming an adhesive layering, the servant 6 and the via layer 4a, 4b, 6 will be polarized; §, for example, the step of bonding the transparent substrate 1, 2 . The shapes of the subsequent agent layers 4a, 4b, 6 are carried out under reduced pressure. Specific examples of the method for producing a polarizing plate of Fig. 5 are as follows. (1) The polarizer 3 (4) of the intermediate A which is laminated in the order of the transparent substrate i, the adhesive layer 4a, and the polarizer 3a is not formed with the surface of the adhesive layer 4a (hereinafter referred to as the middle) The adhesive layer 6 is formed on the polarizer surface of the body A, and the adhesive layer 6 is laminated with the intermediate body B in the order of the transparent substrate 2, the adhesive layer 4b, and the polarizer 3b. A method of joining the surface of the adhesive layer 4b (hereinafter sometimes referred to as a polarizer surface of the intermediate B). (2) A method of forming the adhesive layer 6 on the polarizer surface of the intermediate b and bonding the polarizer faces of the intermediate body A. (3) A method of joining the polarizer surface of the intermediate B to the adhesive layer 6 of the intermediate c which is laminated in the order of the transparent substrate i, the adhesive layer, the polarizer 3a, and the adhesive layer 6. (4) A method of joining the polarizer surface of the inter-substrate A to the intermediate (four) interface layer 6 in which the transparent substrate 2, the adhesive polarizer 3b, and the adhesive layer 6 are laminated in this order. The layered storm LI money shines fresh 3&, then the fine 6, the foot 3b sequence of the intermediate E, the polarizer ^ does not form the adhesive layer 6 4 followed by the 4a, and the adhesive layer ^ and the transparent substrate i 320867 22 200937053 Joining to form medium (4), then, on the surface of the (4) _: layer: (hereinafter sometimes referred to as the polarizer surface S of the intermediate F, the splicer layer 4b, and then bonding the fourth (4) 4b to the transparent substrate 2 (6) The adhesive layer 4b is formed on the surface of the polarizing n 3b of the intermediate E where the adhesive layer is not formed, and the intermediate layer G is formed by the adhesive layer 4b and the transparent substrate. Then, no adhesive is formed in the polarizer 3a; The surface of 6 (hereinafter sometimes referred to as the polarizer surface of the intermediate G) forms two

Ο 著劑層4a ’並將接著劑層4a與透明基板】接合的方法。 ⑺在透板1上形成接著_ &amp;,並將接著劑声 4a與中間體g的偏振器面接合的方法。 ⑻在透明基板2上形成接著劑層扑,並將接著劑層 4b與中間體ρ的偏振器面接合的方法。 作為中間體A的製造方法’可以列舉在偏振器如的單 面上形成接著劑層4a,將接著劑層知和透明基板i接合 的方法;或在透明基板丨的單面形成接著劑層4a,將接著 劑層4a和偏振器3a接合的方法。 作為中間體B的製造方法,可以列舉在偏振器3 b的單 面上形成接著劑層4b,並將接著劑層4b和透明基板2接 合的方法;或在透明基板2的單面形成接著劑層4b,並將 接著劑層4b和偏振器3b接合的方法。 作為中間體C的製造方法,可以列舉在偏振器3a的單 面上形成接著劑層4a,並在偏振器3a的另一面上形成接 著劑層6 ’將接著劑層4a和透明基板丨接合的方法;或在 中間體A的偏振器面上形成接著劑層6的方法。 23 320867 200937053 作為中間體D的製造方法’可以列舉在偏振器%的單 面上形成接著劑層4b,並在偏振器3b的另—面上形成接 、 著劑層6,將接著劑層4b和透明基板2接合的方法;或在 · 中間體B的偏振器面上形成接著劑層6的方法。 第6圖和第7圖表示具有2片偏振器的偏振片之其它 實施形態。第6圖的偏振片是透明基板2的面積小於偏振 器3a、3b和接著劑層4a、4b、6時的例子,位於透明基板 1和透明基板2的狹窄部的偏振器3a、3b和接著劑層4a、 4b、6的外周部被密封劑7被覆。第7圖的偏振片是透明 ❹ 基板1、2的面積小於偏振器3a、3b和接著劑層4a、4b、 6時的例子,從透明基板1和透明基板2向外突出的偏振 器3a、3b和接著劑層4a、4b、6的外周部被密封劑7被覆。 第8圖和第9圖表示具有2片偏振器的偏振片之另外 的其它實施形態。第8圖的偏振片與第5圖的偏振片的不 同點在於:在偏振器3a、3b的與接著劑層4a、4b相接的 面的相反側之面上,分別形成保護層9a、9b,這些保護層 ❹ 9a、9b是用接著劑層6接合。 關於第8圖的偏振片,接著劑層4a與接著劑層6的玻 璃移轉溫度、以及接著劑層6與接著劑層4b的玻璃移轉溫 度是分別不同。由此’由於熱等而在偏振片内部產生的應 力變形,係被玻璃移轉溫度不同的接著劑層4a、4b、6所 吸收、緩和,可以有效地抑制偏振器等剝離等的不良情況。 同時’接著劑層4a、接著劑層4b、接著劑層6的適合玻璃 移轉溫度是與第5圖的情況相同。 24 320867 200937053 •作為本發明中使用的保護層9a、9b的材質,可襄 如.乙稀-酸野共聚物(例如BYNEL(註冊商標、杜邦公 !聚婦烴系接著劑、環氧樹脂系接著劑、聚IU旨樹脂系接 如麵公司製的紫外固化型樹脂、商品名“^^,(例 2線固化型魏燒,♦氧燒RTV,雜膠,具 基末端㈣的改質錢域脂)、氰基丙烯 = Ο :脂等紫外線固化性接著劑。其中,從能夠防止二= 、明基板卜2與偏振器3a、3b之間的觀點而言益冷 劑型的接著劑為佳。 …&amp; 向偏振器3a、3b形成保護層9a、9b可例示,將形 膜狀的保護層9a、9b貼合到偏振器3a、3b而形成,或者 在偏振器3a、3b的表面塗布作為保護層9a、9b的固^性 樹脂並固化而形成。向偏振器3a、3b形成保護層如、% 可以是偏振器3a、3b接合到透明基板1、2的前步驟,也 〇可以是後步驟。經由在偏振器3a、3b上形成保護層9a、 9b’偏振器3a、3b的機械強度能提高,製造中的收率提高。 進而’可以防止投射型液晶顯示裝置在長期使用中偏振器 3a、3b之產生裂紋。 當偏振器3a、3b的基材為由pva所做成,保護層9a、 9b是塗布固化性樹脂並經固化而成時,作為所使用的固化 性樹脂以熱固化性樹脂和紫外固化性樹脂為佳、另外’此 時,由於在固化步驟中無需高溫狀態,因而不會使偏振片 的光學性能降低,因此特別以紫外固化性樹脂為佳。此外, 25 320867 200937053 保護層9a、9b的厚度以在0. 1 // m至30 # m為宜,更佳為 1/zm至20/zm。保護層9a、9b的厚度為以上時, 偏振器3a、3b的機械強度提高,可以防止偏振器3a、3b 的破損,保護層9a、9b的厚度為30 以下時,由於可以 將偏振器3a、3b因吸光而產生的熱有效率地傳導到透明基 板1,2,結果偏振片的耐光性得以提高。 第9圖的偏振片,在透明基板1、2上經由接著劑層 4a、4b安裝偏振器3a、3b,進而在偏振器3a、3b上形成 保護層9a、9b。接著,保護層9a、9b為挾著透明基板10 用接著劑層6a、6b接合。並且,偏振器3a、3b的露出部 分用密封劑7封固。與第8圖的偏振片相同,接著劑層4a 與接著劑層6a的玻璃移轉溫度、以及接著劑層6b與接著 劑層4b的玻璃移轉溫度分別不同。接著劑層4a、4b、6a、 6b的適合玻璃移轉溫度是與第5圖的情況相同。藉由如此 之構成,偏振器3a、3b產生的熱除了向透明基板1、2傳 導外,還傳向透明基板10,進一步促進偏振器3a、3b的 排熱。 接著,說明關於本發明的光學構件。本發明的光學構 件是將上述的偏振片和相位差膜接合而成的,在以上說明 的偏振片中的透明基板的外表面上,接合相位差膜而成。 即,光學構件是在本發明的偏振片的第1透明基板的與第 1接著劑層相接的面之相反侧的面、以及第2透明基板的 與第2接著劑層相接的面之相反侧的面中,選擇至少一面 上,接合相位差膜而成。第10圖表示本發明光學構件的一 26 320867 200937053 •例。第10圖的光學構件是在第2圖所示的偏振片的透明基 板3的表面經由接著劑層11接合相位差膜12。其中,作 為形成接著劑層11的接著劑,可以列舉如:彈性接著劑、 膠黏劑、固化性接著劑,其中以使用固化性接著劑為適合。 作為在本發明中使用的相位差膜12者,沒有特別限 定,可以使用以往習知的相位差膜。作為相位差膜12者, 可以使用例如傾斜取向(傾斜配向)或混合配向(Hybrid配 向)的盤形液晶(Discatic Liquid Crystals)為由在交聯的 ® 透明有機高分子所成的基質所保持的相位差膜。作為相位 差膜的基質材料,通常,三乙醯纖維素聚碳酸酯、或聚對 苯二曱酸乙二酯等耐環境性、耐試劑性優異的有機高分子 膜是適合的。 本發明的偏振片例如可以使用在具有液晶顯示面板 (以下有時記為“LCD面板”)的投射型液晶顯示裝置(投影 機)等之中。以第13圖所示的背投影機的光學系統為例對 ❹其進行詳細說明。 以高壓水銀燈111作為光源的光束,首先由第1透鏡 陣列112、第2透鏡陣列113、偏振光轉換元件114、重疊 透鏡115進行在反光束斷面的亮度均勻化和偏振化。具體 而言,從光源111射出的光束被將微小透鏡112a配置成矩 陣狀的第1透鏡陣列112分割成多個微小的光束。第2透 鏡陣列113和重疊透鏡115係具有以各個被分割的光束照 射作為照明對象的三個LCD面板140R、140G、140B之整體 的方式,因此,各LCD面板入射侧表面形成整體大體均勻 27 320867 200937053 的照度。 偏振光轉換元件114通常由偏振光束分離器陣列所構 成’配置在第2透鏡陳列113與重疊透鏡115之間。由此, 預先將來自光源的無規偏振光轉換成具有特定偏振方向的 偏振光,減少在後述的入射側偏振片的光量損失,從而發 揮提高畫面亮度的作用。 焭度均勻化和偏振化的光經過反射鏡122,並依次通 過為了分離成RGB三原色的分色鏡121、123、132,分離 成紅色光路、綠色光路、藍色光路,分別入射到LCD面板 ❹ 140R、140G、140B。 關於LCD面板140R、140G、140B,在其入射側和射出 侧分別配置本發明的偏振片(入射侧)142和偏振片(射出 侧)143。 說明關於在RGB各光路中夾著液晶面板所配置在入射 側和射出側的2片偏振片。配置於各光路的偏振片(入射 侧)142和偏振片(射出侧)143,係以與其吸收轴平行的構❹ 成來配置,發揮在配置於各光路的各LCD面板i4〇R、l4〇G、 140B中經由圖像信號將按照各像素進行控制的偏振狀態轉 換成光量的功能。 本發明的偏振片採用紅色光路、綠色光路、藍色光路 的所有光路的共通構成,無論在哪個光路作為耐久性優異 的偏振片較有效的’其中藍色光路、綠色光路特別有效。 此外,偏振片所含的第i透明基板和第2透明基板中的至 少一方為單晶透明基板時’以單晶透明基板成為LCD面板 320867 28 200937053 側的方式設置偏振片為宜。進而,LCD面板的射出側和入 射侧都設有偏振片時’射出側和入射侧的偏振片都以單晶 透明基板侧設置在LCD面板側為佳。 對應於LCD面板140R、140G、140B的圖像數據,對每 個像素以不同的透過率使入射光透過,由此製成的光學像 經由十子形分色鏡150合成,並經由投射透鏡1 了〇擴大投 射到螢幕180上。 ’、 實施例 © 以下例示實施例,更詳細地說明本發明,但本發明並 不受限於這些實施例。 (實施例1) 作為實施例1者,如下製作具有第2圖所示結構的偏 振片。首先,將聚乙烯醇膜(Kuraray公司製、商品名 “VF-PX” 、以下記為“PVA膜,’)單軸拉伸,用多偶氮系 的吸收藍色的染料進行染色,使之乾燥,得到投影機藍色 〇光路用的偏振器3。偏振器3的厚度為28_,44〇咖處的 偏振度為99.9%,吸收軸方向的透過率為。 經由由作為接著劑A的丙烯酸系膠黏劑(Lintec公司 製、玻璃移轉溫度為-50°C、以下記為“膠黏劑1”)所成 的接著劑層4,將如此得到的偏振器3的一面,接合到透 明基板(厚度〇. 5mni的青板玻璃基板(矽酸鹽玻璃))〗上。 接著,用6(TC的烘箱乾燥24小時,將偏振器3的水分量 凋整到5重量%以下。接著’經由由作為接著劑β之環氧 系紫外固化性樹脂(ADEKA公司製、商品名“KR695A” 、玻 320867 29 200937053 璃移轉溫度為90°C)所成的接著劑層5,在減壓下將透明基 板(厚度0. 5mm的藍寶石基板、Kyocera公司製、熱傳導率 40W/mK ) 2接合於偏振器3的另一面。然後,以覆蓋偏振器 3的露出部分的方式,在減壓下塗布由紫外固化性環氧樹 脂(Three bond公司製、商品名“TB3025G” 、透濕度 l〇g/m2 · 24hr)所成的密封劑7,使之固化,得到第2圖所 示結構的偏振片。另外,對所用的藍寶石基板和青板玻璃 基板的與空氣接觸的面’實施利用真空蒸鍍形成介電體5 層的防止反射處理。 〇 〈初期耐光性評估〉 為了評估所製成的偏振片的耐光性,將所製成的偏振 片以偏振片的透明基板1的面位於LCI)面板側的方式投入 到第14圖所示的耐光性評估裝置的藍色光路用的光路 中’開始進行光照射’調查有無因劣化導致的光洩漏的發 生(以下稱為“初期評估,,)。結果表示於表2。表中,“〇,, 表示評估開始經過24小時後光洩漏小於G. 5%,沒有光導 ❹ 致的劣化,“x”表示評估開始經過24小時後光洩漏為〇· 5 %以上,有光導致的劣化。 〈長期耐光性評估〉 將得到的偏振片在60。(:、相對濕度90%的環境下放置 72小時後,進行同樣的耐光性評估(以下稱為“長期評 估”)。 〈耐熱性評估〉 為了評估所製成的偏振片的耐熱性,將偏振片在110 30 320867 200937053 °C的環境Τ保存72小時後,觀察偏振衫舖離(以下稱 為耐熱性試驗)。結果表示於表2。表中,“〇”表示 偏振器沒有剝離、耐熱性健,“X”表示看到偏振器的剝 離,耐熱性差。 1響另外第14圖的_光性評估裝置以飛利浦公司製的 蘭的高壓水銀燈作為光源2q,具有偏振光束分離 Ο 23、雙凸透鏡25等與背投電視的光學系統相同的光學系 統’作為向偏振片26的照射光量,每W為3 0W。1中 韻漏是指投入到耐光性評估裝置後引起的偏振片別的 4化現象,吸收财㈣麵率上制縣。將評估對象 的偏振片和正常的偏振片配置成正交偏抓r〇ssed mcols)時,本來應透過率低的偏振絲現為錢漏而透 過。 (實施例2至8) 透明基板卜透明基板2、密封劑7、接著劑A和接著 ❿劑B使用表1所示的物質,偏振器3的乾燥條件在表丄所 記載的條件下進行,除此之外,其餘與實施例丨同樣地製 作偏振片。對所製成的偏振片與實施例Ί同樣地評估。結 果表示於表1和2〇 另外’表1中的膠黏劑2”是指丙烯酸系勝黏劑 (Lintec公司製、玻璃移轉溫度-6〇t:),“XNR5542”是指 環氧系紫外固化性樹脂(Nagase Chemtex公司製、商品名、 玻璃移轉溫度為105。〇,“KR695B”是指環氧系紫外固化 性樹脂(ADEKA公司製、商品名KR695B、玻璃移轉溫度為 320867 31 200937053 95°C ) ’ “ XNR5516Z”是指紫外固化性環氧樹脂(Nagase -Chemtex 公司製、商品名、透濕度 l〇g/m2.24hr),“EP582” 是指紫外固化性環氧樹脂(Cemedin公司製、商品名、透濕 度 20g/m2 · 24hr)。 (實施例9) 除了作為第2圖的偏振器3,係使用由聚乙烯醇/聚乙 烯嵌段共聚物所成的偏振器以外,其餘與實施例1同樣地 操作’可以得到本發明的偏振片。 (比較例1) 〇 作為接著劑A和B,均使用環氧系紫外固化性樹脂 (ADEKA公司製、商品名“KR695A” 、玻璃移轉溫度為90 C) ’除此以外’其餘與實施例1同樣地製作偏振片。結果 表示於表1和2。將所製成的偏振片在iio°c的環境下保存 72小時’結果看到偏振器剝離,確認耐熱性差。 32 320867 200937053 •表i 透明基板 1 透明基板 2 接著劑A 接著劑B 密封劑 ---r——. 乾燥條件 實施例 1 藍寶石 青板玻璃 膠黏劑1 KR695A TB3025G ------ 60°Cx24 小時 實施例 2 藍寶石 水晶 膠黏劑1 KR695A TB3025G 5〇°Cx72 小時 實施例 3 水晶 水晶. 膠黏劑1 KR695A TB3025G 70°〇12小時 實施例 4 水晶 青板玻鴇 膠黏劑1 XNR5542 XNR5516Z 80°Cx48 小時 實施例 5 藍寶石 青板玻g 膠黏劑2 XNR5542 XNR5516Z 80°〇48小時 實施例 6 氧化鎂 氧化鎂 膠黏劑2 XNR5542 XNR5516Z 80°〇24小時 實施例 7 氧化鎂 ----- 尖晶石 —---- 膠黏劑2 KR695B EP582 80°〇24小時 實施例 8 氡化鎂 尖畢石 —-----_ 膠黏劑2 KR695B EP582 80°Cx6小時 比較例 1 —--- 藍寶石 青板破鴇 ---- KR695A KR695A TB3025G 60°Cx24 小時 ----- i ❹ 33 320867 200937053 表2A method of bonding the adhesive layer 4a' and bonding the adhesive layer 4a to the transparent substrate. (7) A method of forming a subsequent _ &amp; and bonding the adhesive sound 4a to the polarizer surface of the intermediate g on the transparent plate 1. (8) A method of forming an adhesive layer on the transparent substrate 2 and bonding the adhesive layer 4b to the polarizer surface of the intermediate p. The method for producing the intermediate A can be exemplified by a method in which an adhesive layer 4a is formed on one surface of a polarizer, a bonding layer is known to be bonded to the transparent substrate i, or an adhesive layer 4a is formed on one side of the transparent substrate. A method of joining the adhesive layer 4a and the polarizer 3a. The method for producing the intermediate B includes a method of forming the adhesive layer 4b on one surface of the polarizer 3b, and bonding the adhesive layer 4b and the transparent substrate 2; or forming an adhesive on one side of the transparent substrate 2. Layer 4b, and a method of joining the adhesive layer 4b and the polarizer 3b. As a method for producing the intermediate C, an adhesive layer 4a is formed on one surface of the polarizer 3a, and an adhesive layer 6' is formed on the other surface of the polarizer 3a. The adhesive layer 4a and the transparent substrate are bonded. Method; or a method of forming an adhesive layer 6 on the polarizer face of Intermediate A. 23 320867 200937053 As a method for producing the intermediate D, it is exemplified that the adhesive layer 4b is formed on one surface of the polarizer %, and the adhesive layer 6 is formed on the other surface of the polarizer 3b, and the adhesive layer 4b is formed. A method of bonding to the transparent substrate 2; or a method of forming the adhesive layer 6 on the polarizer surface of the intermediate B. Fig. 6 and Fig. 7 show other embodiments of a polarizing plate having two polarizers. The polarizing plate of Fig. 6 is an example in which the area of the transparent substrate 2 is smaller than that of the polarizers 3a, 3b and the adhesive layers 4a, 4b, 6, the polarizers 3a, 3b located at the narrow portions of the transparent substrate 1 and the transparent substrate 2, and then The outer peripheral portions of the agent layers 4a, 4b, and 6 are covered with a sealant 7. The polarizing plate of Fig. 7 is an example in which the area of the transparent ruthenium substrate 1, 2 is smaller than that of the polarizers 3a, 3b and the adhesive layers 4a, 4b, 6, the polarizer 3a which protrudes outward from the transparent substrate 1 and the transparent substrate 2, The outer peripheral portion of the 3b and the adhesive layers 4a, 4b, and 6 is covered with the sealant 7. Fig. 8 and Fig. 9 show still another embodiment of a polarizing plate having two polarizers. The polarizing plate of Fig. 8 is different from the polarizing plate of Fig. 5 in that protective layers 9a, 9b are formed on the opposite sides of the faces of the polarizers 3a, 3b that are in contact with the adhesive layers 4a, 4b, respectively. These protective layers a 9a, 9b are joined by the adhesive layer 6. Regarding the polarizing plate of Fig. 8, the glass transition temperature of the adhesive layer 4a and the adhesive layer 6, and the glass transition temperature of the adhesive layer 6 and the adhesive layer 4b are different. Thus, the stress deformation occurring inside the polarizing plate due to heat or the like is absorbed and relaxed by the adhesive layers 4a, 4b, and 6 having different glass transition temperatures, and it is possible to effectively suppress problems such as peeling of the polarizer or the like. At the same time, the suitable glass transition temperature of the adhesive layer 4a, the adhesive layer 4b, and the adhesive layer 6 is the same as in the case of Fig. 5. 24 320867 200937053 • As the material of the protective layers 9a and 9b used in the present invention, for example, an ethylene-acid field copolymer (for example, BYNEL (registered trademark, DuPont, polyglycolic binder, epoxy resin) The following agent and poly IU resin are connected to UV-curable resin manufactured by Rugao Co., Ltd., and the product name is "^^, (example 2 line curing type Wei burning, ♦ oxygen burning RTV, miscellaneous rubber, with base end (four) modification money) An ultraviolet curable adhesive such as cyanoacrylate or cyanopropylene; Ο: an epoxy-curable adhesive such as a fat. Among them, a good-coolant type adhesive is preferable from the viewpoint of preventing the difference between the two substrates and the polarizers 3a and 3b. The formation of the protective layers 9a and 9b to the polarizers 3a and 3b can be exemplified by bonding the protective layers 9a and 9b in the form of a film to the polarizers 3a and 3b, or coating the surfaces of the polarizers 3a and 3b. It is formed as a curing resin of the protective layers 9a and 9b and cured. Forming a protective layer to the polarizers 3a and 3b, for example, % may be a step before the polarizers 3a, 3b are bonded to the transparent substrates 1, 2, or may be Post-step. Mechanical strength via the formation of protective layers 9a, 9b' polarizers 3a, 3b on polarizers 3a, 3b It is possible to improve the yield in the production. Further, it is possible to prevent cracking of the polarizers 3a and 3b during long-term use in the projection type liquid crystal display device. When the substrates of the polarizers 3a and 3b are made of pva, the protective layer is formed. When 9a and 9b are cured by applying a curable resin, it is preferable to use a thermosetting resin and an ultraviolet curable resin as the curable resin to be used, and additionally, at this time, since a high temperature state is not required in the curing step, The optical property of the polarizing plate is not lowered, so that the ultraviolet curable resin is particularly preferable. Further, the thickness of the protective layer 9a, 9b is preferably 0.11 m to 30 #m, more preferably When the thickness of the protective layers 9a and 9b is equal to or greater than that, the mechanical strength of the polarizers 3a and 3b is improved, and the polarizers 3a and 3b can be prevented from being damaged. When the thickness of the protective layers 9a and 9b is 30 or less, the thickness of the protective layers 9a and 9b is 30 or less. Since the heat generated by the light absorption by the polarizers 3a and 3b can be efficiently conducted to the transparent substrates 1, 2, the light resistance of the polarizing plate can be improved. The polarizing plate of Fig. 9 is passed through the transparent substrates 1 and 2 via The agent layer 4a, 4b is installed The polarizers 3a and 3b further form protective layers 9a and 9b on the polarizers 3a and 3b. Then, the protective layers 9a and 9b are bonded to the transparent substrate 10 by the adhesive layers 6a and 6b, and the polarizers 3a and 3b are bonded. The exposed portion is sealed with a sealant 7. As with the polarizing plate of Fig. 8, the glass transition temperature of the adhesive layer 4a and the adhesive layer 6a, and the glass transition temperature of the adhesive layer 6b and the adhesive layer 4b are respectively The suitable glass transition temperatures of the adhesive layers 4a, 4b, 6a, 6b are the same as in the case of Fig. 5. With such a configuration, the heat generated by the polarizers 3a and 3b is transmitted to the transparent substrate 10 in addition to the transparent substrates 1, 2, and the heat dissipation of the polarizers 3a and 3b is further promoted. Next, an optical member relating to the present invention will be described. In the optical member of the present invention, the polarizing plate and the retardation film are joined together, and a retardation film is bonded to the outer surface of the transparent substrate in the polarizing plate described above. In other words, the optical member is a surface on the opposite side of the surface of the first transparent substrate of the polarizing plate of the present invention that is in contact with the first adhesive layer, and a surface of the second transparent substrate that is in contact with the second adhesive layer. On the opposite side, at least one side is selected to join the retardation film. Fig. 10 shows an example of an optical member of the present invention, 26 320 867 200937053. In the optical member of Fig. 10, the retardation film 12 is bonded to the surface of the transparent substrate 3 of the polarizing plate shown in Fig. 2 via the adhesive layer 11. In addition, examples of the adhesive for forming the adhesive layer 11 include an elastic adhesive, an adhesive, and a curable adhesive, and a curable adhesive is preferably used. The retardation film 12 used in the present invention is not particularly limited, and a conventional phase difference film can be used. As the retardation film 12, for example, discotic liquid crystals of oblique orientation (inclined alignment) or mixed alignment (hybrid alignment) can be used as a matrix held by a crosslinked ® transparent organic polymer. Phase difference film. As the matrix material of the retardation film, an organic polymer film excellent in environmental resistance and chemical resistance such as triethylenesulfonate polycarbonate or polyethylene terephthalate is suitable. The polarizing plate of the present invention can be used, for example, in a projection type liquid crystal display device (projector) having a liquid crystal display panel (hereinafter sometimes referred to as "LCD panel"). The optical system of the rear projector shown in Fig. 13 will be described in detail as an example. The light beam having the high-pressure mercury lamp 111 as a light source is firstly uniformized and polarized in the cross-beam cross section by the first lens array 112, the second lens array 113, the polarization conversion element 114, and the superimposing lens 115. Specifically, the light beam emitted from the light source 111 is divided into a plurality of minute light beams by the first lens array 112 in which the minute lenses 112a are arranged in a matrix. The second lens array 113 and the superimposing lens 115 have a form in which the three divided panels are irradiated with the entire three LCD panels 140R, 140G, and 140B as illumination objects, and therefore, the incident side surfaces of the respective LCD panels are formed into a substantially uniform overall shape. Illumination of 200937053. The polarization conversion element 114 is generally disposed between the second lens array 113 and the superimposing lens 115 by the polarization beam splitter array. As a result, the randomly polarized light from the light source is converted into polarized light having a specific polarization direction in advance, and the amount of light loss in the incident side polarizing plate to be described later is reduced, thereby increasing the brightness of the screen. The uniformized and polarized light passes through the mirror 122, and sequentially passes through the dichroic mirrors 121, 123, and 132 for separating into three primary colors of RGB, and is separated into a red light path, a green light path, and a blue light path, and respectively incident on the LCD panel. 140R, 140G, 140B. Regarding the LCD panels 140R, 140G, and 140B, the polarizing plate (incidence side) 142 and the polarizing plate (ejecting side) 143 of the present invention are disposed on the incident side and the outgoing side, respectively. Two polarizing plates which are disposed on the incident side and the output side with the liquid crystal panel interposed therebetween in each of the RGB optical paths will be described. The polarizing plate (incidence side) 142 and the polarizing plate (injecting side) 143 disposed in the respective optical paths are arranged in parallel with the absorption axis, and are displayed on the respective LCD panels i4〇R, l4 disposed in the respective optical paths. In G and 140B, a polarization state controlled by each pixel is converted into a light amount via an image signal. The polarizing plate of the present invention has a common configuration of all the optical paths of the red light path, the green light path, and the blue light path, and is particularly effective in which the optical path is effective as a polarizing plate excellent in durability. Among them, the blue light path and the green light path are particularly effective. When at least one of the i-th transparent substrate and the second transparent substrate included in the polarizing plate is a single crystal transparent substrate, it is preferable to provide a polarizing plate such that the single crystal transparent substrate is on the side of the LCD panel 320867 28 200937053. Further, when both the emission side and the incident side of the LCD panel are provided with the polarizing plate, it is preferable that the polarizing plate on both the emitting side and the incident side is provided on the side of the LCD panel with the single crystal transparent substrate side. Corresponding to the image data of the LCD panels 140R, 140G, and 140B, the incident light is transmitted through each of the pixels at different transmittances, and the optical image thus produced is synthesized via the dichroic dichroic mirror 150 and passed through the projection lens 1 The 〇 is expanded onto the screen 180. EXAMPLES The following examples are given to illustrate the invention in more detail, but the invention is not limited thereto. (Example 1) As Example 1, a polarizing plate having the structure shown in Fig. 2 was produced as follows. First, a polyvinyl alcohol film (manufactured by Kuraray Co., Ltd., trade name "VF-PX", hereinafter referred to as "PVA film,") is uniaxially stretched, and dyed with a polyazo-based blue-absorbing dye to make it Drying, a polarizer 3 for a blue light path of the projector is obtained. The thickness of the polarizer 3 is 28 mm, and the degree of polarization at 44 〇 is 99.9%, and the transmittance in the absorption axis direction is passed through acrylic acid as the adhesive A. The adhesive layer 4 made of an adhesive (manufactured by Lintec, glass transition temperature: -50 ° C, hereinafter referred to as "adhesive 1"), and one side of the polarizer 3 thus obtained is bonded to the transparent layer The substrate (thickness 〇. 5mni of the slate glass substrate (silicate glass)). Next, the moisture of the polarizer 3 is reduced to 5% by weight or less by drying in a 6 (TC oven for 24 hours. The adhesive layer 5 formed by an epoxy-based ultraviolet curable resin (manufactured by Adeka Co., Ltd., trade name "KR695A", glass 320867 29 200937053 glass transition temperature: 90 ° C) as an adhesive β under reduced pressure Transparent substrate (sapphire substrate with a thickness of 0.5 mm, manufactured by Kyocera, heat conduction) The ratio of 40 W/mK was bonded to the other side of the polarizer 3. Then, the ultraviolet curable epoxy resin (manufactured by Three Bond Co., Ltd., trade name "TB3025G" was applied under reduced pressure so as to cover the exposed portion of the polarizer 3. The sealant 7 formed by the moisture permeability l〇g/m2 · 24 hr was solidified to obtain a polarizing plate having the structure shown in Fig. 2. In addition, the air contact between the sapphire substrate and the blue plate glass substrate used was The surface of the dielectric layer is subjected to vacuum deposition to form an antireflection treatment for the dielectric layer. 〇 <Evaluation of initial light resistance> In order to evaluate the light resistance of the prepared polarizing plate, the polarizing plate thus produced is transparent to the polarizing plate. In the optical path for the blue light path of the light resistance evaluation device shown in FIG. 14 , the surface of the substrate 1 is placed on the LCI panel side, and the light irradiation is started to investigate whether or not light leakage has occurred due to deterioration (hereinafter referred to as For "initial assessment,,". The results are shown in Table 2. In the table, “〇,” indicates that the light leakage is less than G. 5% after 24 hours of evaluation, and there is no deterioration caused by light guide. “x” indicates that the light leakage is 〇·5% or more after 24 hours of evaluation. (Evaluation of long-term light resistance) The obtained polarizing plate was subjected to the same light resistance evaluation (hereinafter referred to as "long-term evaluation") after leaving it for 60 hours in an environment of 60% relative humidity (hereinafter referred to as "long-term evaluation"). Evaluation of heat resistance> In order to evaluate the heat resistance of the prepared polarizing plate, the polarizing plate was stored in an environment of 110 30 320867 200937053 ° C for 72 hours, and then the polarized shirt was left (hereinafter referred to as heat resistance test). In Table 2. In the table, "〇" indicates that the polarizer is not peeled off and heat resistance is strong, and "X" indicates that the polarizer is peeled off and the heat resistance is poor. 1 The other _photometric evaluation device of Fig. 14 is manufactured by Philips. The blue high-pressure mercury lamp is used as the light source 2q, and has the same optical system as the optical system of the rear projection television, such as the polarization beam splitting Ο 23, the lenticular lens 25, and the like, as the amount of illumination light to the polarizing plate 26, which is 30 W per W. Rhythm leakage refers to the phenomenon of polarization of the polarizing film caused by the light resistance evaluation device, and absorbs the financial (four) surface rate of the county. The polarizing plate of the evaluation object and the normal polarizing plate are arranged to be orthogonally biased by r〇ssed. In the case of mcols), the polarizing filament which should originally have a low transmittance is now transmitted through the leak. (Examples 2 to 8) The transparent substrate, the transparent substrate 2, the sealant 7, the adhesive A, and the subsequent bismuth B are shown in Table 1. A polarizing plate was produced in the same manner as in Example , except that the drying conditions of the polarizer 3 were carried out under the conditions described in the Table 3. The prepared polarizing plate was evaluated in the same manner as in Example 。. The results are shown in Tables 1 and 2, and the other 'Adhesive 2 in Table 1' refers to an acrylic adhesive (made by Lintec, glass transition temperature - 6〇t:), and "XNR5542" means epoxy. UV curable resin (product name, glass transition temperature, manufactured by Nagase Chemtex Co., Ltd., 105. K, "KR695B" means epoxy-based ultraviolet curable resin (trade name KR695B, manufactured by ADEKA CORPORATION, glass transition temperature is 320867 31) 200937053 95°C ) ' “XNR5516Z” means UV solid Epoxy resin (manufactured by Nagase-Chemtex, trade name, moisture permeability l〇g/m2.24hr), and "EP582" means ultraviolet curable epoxy resin (manufactured by Cemedin, trade name, moisture permeability 20g/m2 · (Example 9) The same procedure as in Example 1 was carried out except that the polarizer 3 of Fig. 2 was a polarizer made of a polyvinyl alcohol/polyethylene block copolymer. (Comparative Example 1) 〇 As the adhesives A and B, epoxy-based ultraviolet curable resin (trade name "KR695A", manufactured by ADEKA CORPORATION, glass transition temperature: 90 C) was used. In the same manner as in Example 1, a polarizing plate was produced. The results are shown in Tables 1 and 2. The prepared polarizing plate was stored in an environment of iio °c for 72 hours. As a result, the polarizer was peeled off, and it was confirmed that the heat resistance was poor. 32 320867 200937053 • Table i Transparent substrate 1 Transparent substrate 2 Adhesive A Adhesive B Sealant---r——. Drying conditions Example 1 Sapphire green glass adhesive 1 KR695A TB3025G ------ 60° Cx24 hours Example 2 Sapphire Crystal Adhesive 1 KR695A TB3025G 5〇°Cx72 hours Example 3 Crystal Crystal. Adhesive 1 KR695A TB3025G 70°〇12 hours Example 4 Crystal Green Board Glass Adhesive 1 XNR5542 XNR5516Z 80 °Cx48 hours Example 5 Sapphire Green Glass Glass G Adhesive 2 XNR5542 XNR5516Z 80°〇48 hours Example 6 Magnesium Oxide Oxide Adhesive 2 XNR5542 XNR5516Z 80°〇24 hours Example 7 Magnesium Oxide----- Spinel----- Adhesive 2 KR695B EP582 80°〇24 hours Example 8 Magnesium telluride tipping stone—----_ Adhesive 2 KR695B EP582 80°C×6 hours Comparative example 1—- -- Sapphire Green Board Breaking---- KR695A KR695A TB3025G 60°Cx24 Hours----- i ❹ 33 320867 200937053 Table 2

__5^* 性 耐熱性 初期 -~_ 長期 實施例1 〇 〇 〇 實施例2 〇 〇 〇 實施例3 〇 一 〇 〇 實施例4 〇 〇 〇 實施例5 〇 一 〇 〇 實施例6 1----- 〇 〇 〇 實施例7 〇 〇 〇 實施例8 〇 —-丨_ 〇 〇 比較例1 1 ' — _ • 1 〇 〇 X__5^* Initial heat resistance - _ long-term embodiment 1 〇〇〇 Example 2 〇〇〇 Example 3 〇〇 〇〇 Example 4 〇〇〇 Example 5 〇〇 〇〇 Example 6 1--- - Example 7 〇〇〇 Example 8 〇 - 丨 _ 〇〇 Comparative Example 1 1 ' _ _ 1 〇〇 X

(實施例10) 作為實施例10,如下製作具有第5圖所示結構的偏振 1、,,首先’將PVA膜單轴拉伸,用多偶氮系的吸收藍色的 木料進仃杂色’使之乾燥’分別得到投影機藍色光路用的 ,振器仏和3b。偏振器3a在440nm處的偏振度為32.0❹ %,吸收軸方向的透過率為46 〇%,偏振器扑的偏振度 為99.9%,吸收軸方向的透過率為〇.〇%。 在偏振器3a的單面上塗布形成接著劑層β的接著劑即 丙稀酸系膠黏劑l(Lintex公司製:玻璃移轉溫度_5〇。〇, 將接著劑層6和偏振器3b接合,得到中間體e。在作為透 明,板1的厚度〇.5mm的藍寶石基板的一面上,塗布形成 接者劑層4a的接著劑即紫相化性環氧樹脂⑽福公司 320867 34 200937053 -製、商品名“KR695A” 、玻璃移轉溫度90。〇,將接著劑 層4a和中間體E的偏振器3a的沒有形成接著劑層6的面 接合,得到中間體F。接著,將中間體F用80。(:的烘箱乾 燥24小時後,在作為透明基板2的厚度〇. 5mm的玻璃基板 上塗布形成接著劑層4b的接著劑即環氧系紫外固化性樹 脂(NagaseChemtex公司製、商品名“XNR5542”、玻璃移 轉溫度為105°C),在減壓下將接著劑層4b和中間體f的 〇偏振器面接合。然後,作為密封劑7者,是使用環氧系紫 外固化性樹脂(Three Bond公司製、商品名“TB3〇25G” 、' 透濕度10g/m2 · 24hr),將偏振器3a、偏振器补、接著劑 層4a、接著劑層4b、接著劑層6的露出部分被覆,得到第 5圖所示結構的偏振片。所製成的偏振片的厚度為^ “取 關於如此得到的偏振片,用第14圖所示的耐光性f估 裝置,與實施例1同樣地進行耐級評估(初期評估和 評估)以及耐熱性評估。還進行了小型化的評估。結果表示 © 於表3和表4。 、 〈小型化的評估〉 測定所製成的偏振片的厚度,對能否小型化進行 估。結果示於表2。表中’“〇,,表示偏振片的厚度小 Unnn’能夠小型化’ V表示偏振片的厚度為15咖 上,無法小型化。 (實施例11至22) 除了透明基板卜透明基板2、密封劑7、接著劑層4心 接著劑層4b、接著劑層6使用夹3所千沾仏, 尺用衣d所不的物質,偏振器知、 320E67 35 200937053 3b的乾燥條件在表3所記載的條件下 施例1〇同樣地製作偏振片。接著, 之外’其餘與實 及 行小型化的評估、料性評估(初期評=同樣地進 耐熱性評估。結果表示於表3和表4。長期評估)以 (實施例23) 除了作為偏振器,使用由聚乙_/聚 所成的偏振器以外,立於由.a ^4 Λ _ 乙埽嵌段共聚物 到本發明的偏振片。 樣地操作,可以得 (比較例2)(Example 10) As Example 10, the polarization 1 having the structure shown in Fig. 5 was produced as follows. First, the PVA film was uniaxially stretched, and the blue absorbing wood of the polyazo type was used for the variegated color. 'Make it dry' for the projector's blue light path, vibrator 仏 and 3b, respectively. The polarizer 3a has a degree of polarization of 32.0% at 440 nm, a transmittance of 46 〇% in the absorption axis direction, a polarization degree of 99.9% in the direction of the polarizer, and a transmittance of 〇.〇% in the absorption axis direction. An acrylic adhesive 1 which is an adhesive for forming the adhesive layer β is applied to one surface of the polarizer 3a (manufactured by Lintex Co., Ltd.: glass transition temperature _5 Å. 〇, the adhesive layer 6 and the polarizer 3b) Joining to obtain the intermediate e. On the one side of the sapphire substrate having a thickness of 55 mm which is transparent, the plate 1 is coated with a purple phase-forming epoxy resin (10), which is an adhesive for forming the adapter layer 4a, 320867 34 200937053 - The product name "KR695A" and the glass transition temperature of 90. The adhesive layer 4a and the surface of the polarizer 3a of the intermediate E which are not formed with the adhesive layer 6 are bonded to each other to obtain an intermediate F. Next, the intermediate is obtained. F. After drying in an oven for 80 hours, an epoxy-based ultraviolet curable resin (manufactured by Nagase Chemtex Co., Ltd.) which is an adhesive for forming the adhesive layer 4b is applied to a glass substrate having a thickness of 0.5 mm as a transparent substrate 2. The name "XNR5542", glass transition temperature is 105 ° C), and the bismuth polarizer face of the adhesive layer 4b and the intermediate f are joined under reduced pressure. Then, as the sealant 7, epoxy-based ultraviolet curing is used. Resin (made by Three Bond, trade name "TB3" 25G", 'transparent humidity 10g/m2 · 24hr), the polarizer 3a, the polarizer complement, the adhesive layer 4a, the adhesive layer 4b, and the exposed portion of the adhesive layer 6 are covered to obtain the polarization of the structure shown in Fig. 5. The thickness of the prepared polarizing plate was determined as "the polarizing plate thus obtained, and the light resistance f estimating device shown in Fig. 14 was used to perform the leveling evaluation (initial evaluation and evaluation) in the same manner as in the first embodiment. In addition, the evaluation of the heat resistance was carried out. The results are shown in Tables 3 and 4. The evaluation of miniaturization The thickness of the polarizing plate produced was measured, and the miniaturization was evaluated. In Table 2. In the table, '“〇, indicating that the thickness of the polarizing plate is small Unnn' can be miniaturized'. V indicates that the thickness of the polarizing plate is 15 mm, and cannot be miniaturized. (Examples 11 to 22) In addition to the transparency of the transparent substrate The substrate 2, the sealant 7, the adhesive layer 4, the core adhesive layer 4b, and the adhesive layer 6 are smeared by the clip 3, and the material of the strip is not used. The polarizer knows that the drying conditions of 320E67 35 200937053 3b are Under the conditions described in Table 3, Example 1 was prepared in the same manner as the polarizing plate. Next, the evaluation of the remaining and actual miniaturization, the evaluation of the material (initial evaluation = the same heat resistance evaluation. The results are shown in Table 3 and Table 4. Long-term evaluation) to (Example 23) except as a polarization The polarizer is formed from the .a ^4 Λ _ 埽 埽 block copolymer to the polarizing plate of the present invention, except for the polarizer formed by poly _ / poly. The sample operation can be obtained (Comparative Example 2)

在第5圖所示的偏振片中,接著劑層4a、4Mn6均使 用環氧系紫外固化性樹脂(ADEKA公司製、商品名 _ “KR695A” 、玻璃移轉溫度為9〇。〇,除此以二卜,复餘盥 實施例10同樣地製作偏振片。結果表示於表3和4、。將所 製成的偏振片在1HTC的環境下保存72小時,結果看到偏 振器剝離,確認耐熱性差。 (比較例3) 〇 作為比較例3者,如下製作第12圖所示結構的偏振 片。首先,在與實施例10同樣地得到的偏振器3a和偏振 器3b的兩面,用在羧基改質聚乙烯醇樹脂(產品名:KL318) 中以水溶性聚酿胺環氧樹脂(產品名:Sumirez Resin 65(〇 作為有效成分的接著劑,貼合厚度80/ζιη的乙醯纖維素系 膜(Konica公司製KC8UY、以下稱為8UYTAC)S,製成偏振 膜。在含有偏振器3a的偏振膜的單面經由接著劑層&amp;貼合 0.5mm的藍寶石基板(Keyocera公司製),製成偏振片。此 320867 36 200937053 • ^,在含有偏振器3b的偏賴的單面,經由接著劑層4貼 口 0. 5mm的水晶基板’製成偏振片。將這2片偏振片對著 光8入射的方向如第12圖那樣配置。另外,2片偏振片以 間隔為1mm地進行設置。設置時的、包括偏振片間距的厚 度約為2· 5mm。結果表示於表3和4。 表3 透明某jfe ] 透明基板2 玻璃 黏著劑4a KR695A --- 實施例10 Γ ' &quot;* 〜 實施例11 藍寶石 黏著劑4b 膽5542 密封劑 XNR5516Z 乾燥條件 — 1 80°Cx24 小時 實施例12 Γ — 玻璃 水晶 藍寶石 玻璃 KR695A KR695A 黏著劑1 點著劑1 KNR5542 XNR5516Z 80°Cx24 小時 KNR5542 XNR5516Z 80°Cx24 小時 實施例13 玻瑀 水晶 KR695A ----- 黏著钢1 KNR5542 XNR5516Z 80°Cx48 小時 實施例14 尖晶石 水晶 KR695A 黎著劑1 KNR5542 XNR5516Z 80°Cx48 小時 實施例15 -- 水晶 尖晶石 KR695A 黏著劑1 KNR5542 XNR5516Z 80°Cx48 小時 實施例16 尖晶石 玻璃 KR695A 黏著劑1 KNR5542 XNR5516Z 80°Cx48 小時 實施例17 玻璃 尖晶石 KNR5542 黏著劑2 KR69SA TR302SG 7ners/&gt;iQ .uirt 實施例18 水晶 尖晶石 KNR5542 -----— 黏著劑2 KR695A TB3025G 70°Cx48 小時 實施例19 尖晶石 水畢 KNR5542 黏著劑2 KR695A. TB3025G 70°Cx48 小時 實施例20 藍寶石 水晶 KNR5542 黏著刺2 KR695A TB3025G 90°Cx48 小時 實施例21 水晶 藍寶石 KNR5542 黏著劑2 KR695A TB3025G 90°Cx48 小時 實施例22 一 1 尖晶石 尖晶石 KNR5542 黏著劑2 KR695A TB3025G 90°Cx48 小時 比較例2 藍寶石 玻璃 KR695A KR695A KR695A XNR5516Z 80°Cx48 小時 比較例3 藍寶石 水晶 — — — — 37 320867 200937053 表4In the polarizing plate shown in Fig. 5, an epoxy-based ultraviolet curable resin (trade name "KR695A", manufactured by ADEKA CORPORATION, and a glass transition temperature of 9 Å are used for the adhesive layers 4a and 4Mn6. A polarizing plate was produced in the same manner as in Example 10, and the results are shown in Tables 3 and 4. The prepared polarizing plate was stored in an environment of 1 HTC for 72 hours, and the polarizer was peeled off to confirm heat resistance. (Comparative Example 3) As a comparative example 3, a polarizing plate having the structure shown in Fig. 12 was produced as follows. First, both sides of the polarizer 3a and the polarizer 3b obtained in the same manner as in Example 10 were used for the carboxyl group. Modified polyvinyl alcohol resin (product name: KL318) with water-soluble polyamine resin (product name: Sumirez Resin 65 (〇 as an active ingredient of an adhesive, bonded to a thickness of 80/ζιη of acetaminophen A film (KC8UY, manufactured by Konica Co., Ltd., hereinafter referred to as 8UYTAC) S was used to form a polarizing film, and a 0.5 mm sapphire substrate (manufactured by Keyocera Co., Ltd.) was bonded to one surface of the polarizing film containing the polarizer 3a via an adhesive layer & Polarized sheet. This 320867 36 200937053 • ^ The polarizing plate was formed on the single side of the polarizing layer 3b, and the crystal substrate of the 5 mm crystal substrate was placed through the adhesive layer 4. The direction in which the two polarizing plates were incident on the light 8 was arranged as shown in Fig. 12. In addition, two polarizing plates were disposed at intervals of 1 mm. The thickness including the polarizing plate pitch was about 2.5 mm when set. The results are shown in Tables 3 and 4. Table 3 Transparent Jfe] Transparent substrate 2 Glass adhesion Agent 4a KR695A --- Example 10 Γ ' &quot;* ~ Example 11 Sapphire Adhesive 4b Bile 5542 Sealant XNR5516Z Drying Conditions - 1 80 ° C x 24 hours Example 12 Γ - Glass Crystal Sapphire Glass KR695A KR695A Adhesive 1 point Agent 1 KNR5542 XNR5516Z 80°Cx24 hours KNR5542 XNR5516Z 80°Cx24 hours Example 13 Glass crystal KR695A ----- Adhesive steel 1 KNR5542 XNR5516Z 80°Cx48 hours Example 14 Spinel crystal KR695A Li agent 1 KNR5542 XNR5516Z 80 ° C x 48 hours Example 15 - Crystal spinel KR695A Adhesive 1 KNR5542 XNR5516Z 80 ° C x 48 hours Example 16 Spinel glass KR695A Adhesive 1 KNR5542 XNR5516Z 80 ° Cx48 Hour Example 17 Glass Spinel KNR5542 Adhesive 2 KR69SA TR302SG 7ners/&gt;iQ .uirt Example 18 Crystal Spinel KNR5542 ------ Adhesive 2 KR695A TB3025G 70°C x 48 Hour Example 19 Spinel Water Complete KNR5542 Adhesive 2 KR695A. TB3025G 70°Cx48 Hour Example 20 Sapphire Crystal KNR5542 Adhesive 2 KR695A TB3025G 90°C x 48 Hour Example 21 Crystal Sapphire KNR5542 Adhesive 2 KR695A TB3025G 90°C x 48 Hour Example 22 A 1 Spinel Stone spinel KNR5542 Adhesive 2 KR695A TB3025G 90°Cx48 hours Comparative Example 2 Sapphire glass KR695A KR695A KR695A XNR5516Z 80°Cx48 hours Comparative example 3 Sapphire crystal — — — — 37 320867 200937053 Table 4

、凡本發明的偏振片耐光性優異且能夠小型化。因此,用 於才又^型液晶顯示裝置時’能夠對光學系統的小型化作出 的貝獻,實現馬亮度且長壽命化。此外,本發明的偏振 片的初期耐光性、長期耐光性和耐熱性都優異。 【圖式簡單說明】 第1圖說明具有〗片偏振器的本發明相關偏振片之 成例的圖。 320867 38 200937053 -第2圖說明具有1片偏振器的本發明相關偏振片之其 它構成例的圖(實施例1至8、比較例1的構成圖)。 第3圖說明具有1片偏振器的本發明相關偏振片之其 它構成例的圖。 第4圖說明具有1片偏振器的本發明相關偏振片之其 它構成例的圖。 第5圖說明具有2片偏振器的本發明相關偏振片之構 成例的圖(實施例10至23的構成圖)。 ® 第6圖說明具有2片偏振器的本發明相關偏振片之其 它構成例的圖。 第7圖說明具有2片偏振器的本發明相關偏振片之其 它構成例的圖。 第8圖說明具有2片偏振器的本發明相關偏振片之其 它構成例的圖。 第9圖說明具有2片偏振器的本發明相關偏振片之其 Q 它構成例的圖。 第10圖說明本發明光學構件構成的一例之圖。 第11圖說明以往的偏振片構成圖。 第12圖說明比較例3中使用的偏振片的構成圖。 第13圖投影機光路圖。 第14圖耐光性評估裝置的示意圖。 【主要元件符號說明】 1 透明基板(第1透明基板) 2 透明基板(第2透明基板) 39 320867 200937053 3、 3a、3b偏振器 4、 4a、4b、5、6、6a、6b、11 接著劑層 7 密封劑 8 照射光 9a、 9b保護層 10 透明基板(第3透明基板) 12 相位差膜 20 高壓水銀燈 21 UV/IR截止濾光器 22 複眼透鏡(fey eye lens) 23 偏振光束分離器陣列 24 雙色分光鏡(Dichroic mirror) 25 透鏡 26 樣品支架 27 白色光 28 紅色、綠色光 29 藍色光 111 高壓水銀燈 112 透鏡陣列 112a 微小透鏡 113 透鏡陣列 114 偏振光轉換元件 115 重疊透鏡 121 &gt; 123、132分色鏡 122 反射鏡 134 反射鏡 135 透鏡 140R 紅色用LCD面板 HOG 綠色用LCD面板 140B 藍色用LCD面板 142 偏振片(入射側) 143 偏振片(射出側) 150 十字形分色鏡 170 投射透鏡 180 勞幕The polarizing plate of the present invention is excellent in light resistance and can be miniaturized. Therefore, when it is used in a liquid crystal display device, it is possible to achieve a reduction in brightness and a long life of the optical system. Further, the polarizing plate of the present invention is excellent in initial light resistance, long-term light resistance, and heat resistance. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a view showing an example of a polarizing plate of the present invention having a sheet polarizer. 320867 38 200937053 - Fig. 2 is a view showing another configuration example of the polarizing plate of the present invention having one polarizer (embodiments of Examples 1 to 8 and Comparative Example 1). Fig. 3 is a view showing another configuration example of the polarizing plate of the present invention having one polarizer. Fig. 4 is a view showing another configuration example of the polarizing plate of the present invention having one polarizer. Fig. 5 is a view showing a configuration example of the polarizing plate of the present invention having two polarizers (constitution views of Examples 10 to 23). ® Fig. 6 is a view showing another configuration example of the polarizing plate of the present invention having two polarizers. Fig. 7 is a view showing another configuration example of the polarizing plate of the present invention having two polarizers. Fig. 8 is a view showing another configuration example of the polarizing plate of the present invention having two polarizers. Fig. 9 is a view showing an example of the constitution of the polarizing plate of the present invention having two polarizers. Fig. 10 is a view showing an example of the configuration of an optical member of the present invention. Fig. 11 is a view showing a configuration of a conventional polarizing plate. Fig. 12 is a view showing the configuration of a polarizing plate used in Comparative Example 3. Figure 13 Projector light path diagram. Figure 14 is a schematic view of the light resistance evaluation device. [Description of main components] 1 transparent substrate (first transparent substrate) 2 transparent substrate (second transparent substrate) 39 320867 200937053 3, 3a, 3b polarizers 4, 4a, 4b, 5, 6, 6a, 6b, 11 Agent layer 7 Sealant 8 Irradiation light 9a, 9b Protective layer 10 Transparent substrate (3rd transparent substrate) 12 Phase difference film 20 High pressure mercury lamp 21 UV/IR cut filter 22 Fey eye lens 23 Polarizing beam splitter Array 24 Dichroic mirror 25 Lens 26 Sample holder 27 White light 28 Red, green light 29 Blue light 111 High pressure mercury lamp 112 Lens array 112a Tiny lens 113 Lens array 114 Polarizing light conversion element 115 Overlapping lens 121 &gt; 123, 132 dichroic mirror 122 mirror 134 mirror 135 lens 140R red LCD panel HOG green LCD panel 140B blue LCD panel 142 polarizer (incident side) 143 polarizer (injection side) 150 cross dichroic mirror 170 projection Lens 180

〇 40 320867〇 40 320867

Claims (1)

200937053 ^ 七、申請專利範圍: 1. 一種偏振片,其是至少兩片透明基板相對隔離著,在位 於一方最外侧的第1透明基板與位於另一方最外側的 第2透明基板之間,設有至少一片偏振器的偏振片,其 中, 在上述各偏振器的一方侧設有第1接著劍層,在另 一方侧設有第2接著劑層, 上述第1接著劑層與上述第2接著劑層的玻璃移轉 Ό 溫度為不同。 2. 如申請專利範圍第丨項之偏振片,其中,在前述第j 接著劑層和前述第2接著劑層中,一方接著劑層由彈性 接著劑或膠黏劑形成,另一方接著劑層由固化性接著劑 形成。 3. 如申請專利範圍第1項之偏振片,其中, 在所述第1透明基板與所述第2透明基板之間設有 ❹ 一片偏振器, 所述偏振器籍由所述第1接著劑層與所述第1透明 基板接合,藉由所述第2接著劑層與所述第2透明基板 接合。 4. 如申請專利範圍第1項之偏振片,其中,在所述第1 透明基板與所述第2透明基板相對的内面,分別形成第 1接著劑層,經由戶斤述弟1接著劑層在所述各透明基板 上安裝相.互不同的雨片偏振器。 5. 如申請專利範圍笫4項之偏振片,其中,用第2接著劑 320867 41 200937053 層接合:安裝於所述第1透明基板上的偏振器的與所述 _ 第1接著劑層相接面的相反侧之面、和安裝於所述第2 透明基板上的偏振器的與所述第1接著劑層相接面之 相反側的面。 6. 如申請專利範圍第4項之偏振片’其中,在分別安裝於 所述第1透明基板與所述第2透明基板上的偏振器的, 與所述第1接著劑層相接面的相反侧之面上’分別形成 保護層,所述保護層之間用第2接著劑層接合。 7. 如申請專利範圍第4項之偏振片’其中’在分別安裝於 ◎ 所述第1透明基板與所述第2透明基板上的偏振器的’ 與所述第1接著劑層相接面的相反侧之面上分別形成 保護層,所述保護層之間夾著第3透明基板用第2接著 劑層接合。 8. 如申請專利範圍第4項之偏振片,其中,關於中心波長 為440nm的光,分別安裝於所述第1透明基板與所述第 2透明基板上的偏振器中的/方偏振器的吸收轴方向 ^ 的透過率為10%至70%,另一方偏振器的吸收軸方向 的透過率為1%以下。 9. 如申請專利範圍第4項之偏振片,其中’對於中心波長 為550ηιη的光,分別安裝於所述第1透明基板與所述第 2透明基板上的偏振器中的一方偏振器的吸收軸方向 的透過率為10%至70%,另/方偏振器的吸收轴方向 的透過率為1%以下。 如申請專利範圍第4項之偏振片,其中,對於中心波長 42 320867 200937053 • 為61〇nm的光,分別安裝於所述第1透明基板與所述第 2透明基板上的偏振器中的一方偏振器的吸收軸方向 的透過率為10%至70%,另一方偏振器的吸收軸方向 的透過率為1%以下。 11. 如申請專利範圍第1項之偏振片,其中,所述偏振器的 水分含量為5重量%以下。 12. 如申請專利範圍第丨項之偏振片,其中,所述偏振器是 在聚乙烯醇系樹脂的偏振器基板上吸附配向有二色性 染料或碘的偏振器。 13·如申請專利範圍第1項之偏振片,其中,所述偏振器是 由聚乙婦醇/聚乙_嵌段共聚物所成的膜。 14. 如申請專利範圍第1項之偏振片,其中,所述第i透明 基板和所述第2透明基板中的至少一方的熱傳導率為 5W/(m . 10以上。 15. 如申請專利範圍第1項之偏振片,其中,第丨透明基板 ❹ 和第2透明基板中的一方的材質是選自由水晶、藍寶 石、氧化鎂和尖晶石所成群組中的至少一種,另一方的 材質是選自由氧化鎂、尖晶石、石英玻璃、矽酸鹽玻璃、 硼矽酸鹽玻璃和水晶所成群組中的至少一種。 16·如申請專利範圍第1項之偏振片,其中,所述第(透明 基板和所述第2㈣基板巾的至少―方鮮晶的透明 基板。 Π.-種光學構件纟是將申請專利範圍第丨項至第16項 中任一項之偏振片和相位差骐接合而成。 320867 43 200937053 18· =申請專利範圍第丨項至第16項中任一項之偏振片的 . 製造方法,其具有在減壓下形成第丨接著劑層和/或第 2接著劑層的步驟。 19·如申請專利範圍第18項之製造方法,其還具有在13〇 C以下的溫度乾燥偏振器的步驟。 20.—種投射型液晶顯示裝置,其具有申請專利範圍第i 項至第16項中任—項之偏振片和液晶顯示面板。 1.如申4專利範圍第2G項之投射型液晶顯示震置,其 中’第1透明基板和第2透明基板中的至少—方是單晶❹ 的透明基板’以前述單晶的透明基板成為液晶顯示面板 侧的方式設置所述偏振片。 Ο 320867200937053 ^ VII. Patent Application Range: 1. A polarizing plate in which at least two transparent substrates are relatively isolated, and are disposed between a first transparent substrate located at one outermost side and a second transparent substrate located at the outermost side of the other side. a polarizing plate having at least one polarizer, wherein a first scabbard layer is provided on one side of each of the polarizers, and a second adhesive layer is provided on the other side, the first adhesive layer and the second subsequent layer The glass transition of the layer is different. 2. The polarizing plate according to claim 2, wherein in the j-th subsequent layer and the second adhesive layer, one of the adhesive layers is formed of an elastic adhesive or an adhesive, and the other adhesive layer It is formed of a curable adhesive. 3. The polarizing plate of claim 1, wherein a first polarizer is disposed between the first transparent substrate and the second transparent substrate, and the polarizer is provided by the first adhesive The layer is bonded to the first transparent substrate, and the second adhesive layer is bonded to the second transparent substrate. 4. The polarizing plate of claim 1, wherein the first adhesive layer is formed on the inner surface of the first transparent substrate and the second transparent substrate, and the adhesive layer is formed by the household Different phase wiper polarizers are mounted on the respective transparent substrates. 5. The polarizing plate of claim 4, wherein the second bonding agent 320867 41 200937053 is joined by a layer: a polarizer mounted on the first transparent substrate is in contact with the _ first adhesive layer The surface on the opposite side of the surface and the surface on the opposite side of the surface of the polarizer attached to the second transparent substrate that is in contact with the first adhesive layer. 6. The polarizing plate of claim 4, wherein the polarizer attached to the first transparent substrate and the second transparent substrate is in contact with the first adhesive layer On the opposite side, 'protective layers are respectively formed, and the protective layers are joined by a second adhesive layer. 7. The polarizing plate of claim 4, wherein the 'the polarizer attached to the first transparent substrate and the second transparent substrate' is in contact with the first adhesive layer A protective layer is formed on each of the opposite sides, and the third transparent substrate is bonded to the second transparent substrate via the second adhesive layer. 8. The polarizing plate of claim 4, wherein the light having a center wavelength of 440 nm is respectively mounted on the first transparent substrate and the polarizer in the second transparent substrate The transmittance in the absorption axis direction is 10% to 70%, and the transmittance in the absorption axis direction of the other polarizer is 1% or less. 9. The polarizing plate of claim 4, wherein 'the absorption of one of the polarizers attached to the first transparent substrate and the second transparent substrate for light having a center wavelength of 550 ηηη The transmittance in the axial direction is 10% to 70%, and the transmittance in the absorption axis direction of the other polarizer is 1% or less. The polarizing plate of claim 4, wherein one of the polarizers attached to the first transparent substrate and the second transparent substrate is light having a center wavelength of 42 320867 200937053 • 61 〇 nm The transmittance of the polarizer in the absorption axis direction is 10% to 70%, and the transmittance of the other polarizer in the absorption axis direction is 1% or less. 11. The polarizing plate of claim 1, wherein the polarizer has a moisture content of 5% by weight or less. 12. The polarizing plate according to claim 2, wherein the polarizer is a polarizer that adsorbs a dichroic dye or iodine on a polarizer substrate of a polyvinyl alcohol resin. The polarizing plate of claim 1, wherein the polarizer is a film formed of a polyethylol/poly-block copolymer. 14. The polarizing plate of claim 1, wherein at least one of the i-th transparent substrate and the second transparent substrate has a thermal conductivity of 5 W/(m. 10 or more. 15. In the polarizing plate of the first aspect, the material of one of the second transparent substrate ❹ and the second transparent substrate is at least one selected from the group consisting of crystal, sapphire, magnesia, and spinel, and the other material. Is at least one selected from the group consisting of magnesium oxide, spinel, quartz glass, silicate glass, borosilicate glass, and crystal. 16) The polarizing plate of claim 1, wherein The transparent substrate of the transparent substrate and the second (four) substrate towel is at least a square crystal. The optical member is a polarizing plate and a phase difference according to any one of the above claims. The method of manufacturing a polarizing plate according to any one of the preceding claims, wherein the forming of the second adhesive layer and/or the second subsequent step under reduced pressure is performed. Step of the agent layer. The manufacturing method of claim 18, further comprising the step of drying the polarizer at a temperature of 13 ° C or lower. 20. A projection type liquid crystal display device having any of the claims i to 16 - a polarizing plate and a liquid crystal display panel. 1. The projection type liquid crystal display of the 2Gth item of claim 4, wherein at least one of the first transparent substrate and the second transparent substrate is transparent to the single crystal germanium. The substrate 'the polarizing plate is provided such that the transparent substrate of the single crystal becomes the liquid crystal display panel side. Ο 320867
TW97149635A 2007-12-28 2008-12-19 Polarizer and method for making the same TW200937053A (en)

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