TW201030027A - Molded object for optical use, and lightguide plate and light diffuser both comprising same - Google Patents

Molded object for optical use, and lightguide plate and light diffuser both comprising same Download PDF

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TW201030027A
TW201030027A TW098143189A TW98143189A TW201030027A TW 201030027 A TW201030027 A TW 201030027A TW 098143189 A TW098143189 A TW 098143189A TW 98143189 A TW98143189 A TW 98143189A TW 201030027 A TW201030027 A TW 201030027A
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Taiwan
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styrene
light
resin
mass
based resin
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TW098143189A
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Chinese (zh)
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TWI471341B (en
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Jun Takahashi
Shintaro Watanabe
Hideaki Sakamoto
Makoto Sato
Tetsuya Shinmura
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Denki Kagaku Kogyo Kk
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    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/04Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F212/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02Monomers containing only one unsaturated aliphatic radical
    • C08F212/04Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/06Hydrocarbons
    • C08F212/08Styrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/02Diffusing elements; Afocal elements
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/0001Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings specially adapted for lighting devices or systems
    • G02B6/0011Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings specially adapted for lighting devices or systems the light guides being planar or of plate-like form
    • G02B6/0065Manufacturing aspects; Material aspects

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  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Optics & Photonics (AREA)
  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Optical Elements Other Than Lenses (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Abstract

A molded object for optical use which has low hygroscopicity, is reduced in warpage and dimensional change, has a low loss of light transmittance in a long optical path, and has satisfactory light resistance; and a lightguide plate and a light diffuser both comprising the molded object for optical use. The molded object for optical use is obtained by molding a styrene resin obtained by polymerizing a styrene monomer having a polymerization inhibitor content lower than 10 ppm and a phenylacetylene compound content of 50 ppm or lower.

Description

201030027 六、發明說明: 【發明所屬之技術領域】 本發明係關於-種光學用成形體、使用其之導光板及光 擴散體。 【先前技術】 丙烯酸系樹脂由於透明性優異’故—直被廣泛用作導光 板、擴散板、透鏡等光學用成形體。又,最近,代替丙烯 酸系樹脂,作為光學用成形體亦提出並使用各種苯乙烯系 樹脂® 例如,於專利文獻1中提出有包含以甲基丙烤酸甲酯及 苯乙烯系單體作為主成分之共聚物的樹脂成形體,又,於 專利文獻2中提出有包含苯乙烯_(甲基)丙烯酸酯系共聚合 樹脂之導光板。又,於專利文獻3及專利文獻4中提出有包 含如下共聚物之樹脂組合物,上述共聚物包含芳香族乙稀 系單體及甲基丙稀酸曱醋單體。又,於專利.文獻5中提出 有苯乙烯系聚合物或苯乙烯系單體_甲基丙烯酸曱酯共聚 物之多層擴散板。 [專利文獻1]曰本專利特開2001-342263號公報 [專利文獻2]曰本專利特開2〇〇3_〇75648號公報 [專利文獻3]曰本專利特開2006-052349號公報 [專利文獻4]日本專利特開2006_052350號公報 [專利文獻5]曰本專利特開2007_264598號公報 【發明内容】 丙烯酸系樹脂雖被廣泛用作光學用成形體,但由於吸濕 145347.doc 201030027 佳較尚,故存在容易產生輕曲或尺寸變化之問題。又,丙 烯酸系樹脂因成形時之熱分解性較高,故於高溫下成形之 情开>時’存在成形體中容易產生外觀不良之問題。 針對該等問題’如上所述般提出並使用各種苯乙烯系樹 脂’但苯乙烯系樹脂與丙烯酸系樹脂相比透明性或耐光性 較差,故其使用受到限制。 尤其是存在如下問題:於光學用成形體中,於光線透射 距離較長(以下稱為「長光程」)之用途中之成形體、例如 20吋以上之中〜大型顯示器之導光板中無法使用光透射 率低之笨乙稀系樹脂。 又,作為顯示器光源,一般使用螢光管管 (Fluorescent Lamp))、外部電極管(EEFl 管(External[Technical Field] The present invention relates to a molded article for optics, a light guide plate using the same, and a light diffuser. [Prior Art] Acrylic resin is widely used as an optical molded article such as a light guide plate, a diffusion plate, or a lens because it is excellent in transparency. Further, recently, in place of the acrylic resin, various styrene resins have been proposed and used as the molded article for optics. For example, Patent Document 1 proposes to contain methyl methacrylate and a styrene monomer as main components. In the resin molded article of the copolymer of the component, Patent Document 2 proposes a light guide plate containing a styrene-(meth)acrylate-based copolymer resin. Further, Patent Document 3 and Patent Document 4 propose a resin composition comprising a copolymer comprising an aromatic vinyl monomer and a methyl acetonate monomer. Further, Patent Document 5 proposes a multilayer diffusing plate having a styrene polymer or a styrene monomer-methacrylic acid methacrylate copolymer. [Patent Document 1] Japanese Laid-Open Patent Publication No. 2001-342263 [Patent Document 2] Japanese Patent Laid-Open Publication No. Hei No. Hei. No. Hei. No. Hei. No. 2006-052349. Patent Document 4: JP-A-2006-052350 (Patent Document 5) JP-A-2007-264598 SUMMARY OF THE INVENTION Acrylic resin is widely used as an optical molded body, but it is excellent in moisture absorption 145347.doc 201030027 It is more common, so there is a problem that it is easy to produce a slight curvature or a dimensional change. Further, since the acrylic acid-based resin has high thermal decomposition property at the time of molding, it is difficult to cause an appearance defect in the molded article when it is molded at a high temperature. In view of these problems, various styrene resins have been proposed and used as described above. However, the styrene resin is inferior in transparency or light resistance to the acrylic resin, and its use is limited. In particular, in the molded article for optics, it is not possible to use a molded article in a use in which the light transmission distance is long (hereinafter referred to as "long path length"), for example, a light guide plate of 20 inches or more to a large display. A stupid ethylene resin having a low light transmittance is used. Also, as a display light source, a fluorescent tube (Fluorescent Lamp) and an external electrode tube (EEFl tube (External) are generally used.

Electrode Fluorescent Lamp))、冷陰極管(CCFl 管(ColdElectrode Fluorescent Lamp)), cold cathode tube (CCFl tube (Cold)

Cathode Fluorescent Lamp)),但最近以 LED(Light EmiuingCathode Fluorescent Lamp)), but recently with LED (Light Emiuing

Diode’發光二極體)之技術革新為背景而期望適合於 LED光之新型光學用成形體。 本發明之目的在於提供一種吸濕性較低於長光程中之 光透射率之損耗較少、且耐光性優異之光學用成形體。 又本發明之目的在於提供一種作為液晶顯示器用之導 光板或…、月用t導光;^或者各種光擴散體較為有用的光學 用成形體,尤其是作為以LED為光源之中〜大型液晶顯示 器用之導光板較為有用的導光板、或者於照明等用途中較 為有用之光擴散體。 本發月者就上述課題進行了潛心研究,結果發現,將藉 145347.doc 201030027 由使聚合抑制劑較少、且苯基乙炔系化合物含量較少之苯 乙烯系單體進行聚合所得之苯乙烯系樹脂成形而成的光學 用成形體,其吸濕性較低、於長光程中之光透射率之損耗 較少、且耐光性優異,又,該光學用成形體於導光板或光 擴散體中較為有用,從而完成了本發明。 本發明之光學用成形體係將藉由使聚合抑制劑未達1〇 ppm、且本基乙炔系化合物為ppm以下之苯乙稀系單體 進行聚合反應所得之苯乙烯系樹脂成形而成者。 馨 本發明之光學用成形體、尤其是導光板及光擴散體由於 吸濕性較低故翹曲或尺寸變化較少,於長光程中之光透射 率之損耗較少,且耐光性良好。又,光擴散體之全光線透 射率或擴散率亦良好。 【實施方式】 <用語之說明> 於本申請案說明書中’ 「〜」之符號係指「以上」及 ❿ 「以下」。例如,「A〜B」之記載係指A以上、B以下。 於本說明書中,所謂「光學用成形體」,係指例如利用 於導光板、擴散板、透鏡等光學用途中者。 又’於本說明書中’所謂(甲基)丙烯酸酯系單體,係丙 烯酸酯單體及曱基丙烯酸酯單體之總稱。 又,於本說明書中,所謂「光擴散體」’係指擴散板或 擴散罩所代表之將光加以擴散而以平面或曲面進行面發光 者。 以下,詳細說明本發明之光學用成形體、尤其是導光板 145347.doc 201030027 及光擴散體之實施形態。 本實施形態之光學用成形體係將藉由使聚合抑制劑未達 10 ppm、且苯基乙炔系化合物為5〇 ppm以下之苯乙稀系翠 體進行聚合反應所得之苯乙烯系樹脂成形而成者。 包含上述構成之光學用成形體由於吸濕性較低故勉曲或 尺寸變化較少,於長光程中之光透射率之損耗較少,且耐 光性良好。又,光擴散體之全光線透射率或擴散率亦良 好。 [苯乙烯系樹脂] 笨乙烯系樹脂係將苯乙烯系單體進行聚合而成之聚合 物。 作為苯乙烯系單體,可列舉苯乙烯、α_甲基笨乙烯、對 甲基苯乙烯、鄰甲基笨乙烯、間甲基苯乙烯、乙基苯乙 稀、對第三丁基苯乙稀等,較好的是苯乙稀。該等苯乙稀 系單體可為單獨者,亦可為將兩種以上混合而成者。 苯乙烯系樹脂亦可為苯乙烯系單體與可與苯乙烯系單體 共聚合之單體的共聚物,較好的是將苯乙烯系單體與(甲 基)丙烯酸酯系單體進行共聚合而成之苯乙烯_(曱基)丙烯 酸酯系共聚物。 上述苯乙稀系樹脂為苯乙稀.(甲基)丙稀酸醋系共聚物, 由此可獲得耐光性佳之效果。 作為(甲基)丙稀酸醋系單體,可列舉:(甲基)丙稀酸甲 醋、(甲基)丙稀酸乙醋、(甲基)丙稀酸丁醋、(甲基)丙稀酸 2-乙基己醋之甲基丙烯酸醋’丙烯酸甲醋、丙烯酸乙醋、 145347.doc 201030027 丙浠酸正丁酯、丙烯酸2_甲基己酯、 π坪酸2-乙基己酯、 丙烯酸癸酯等丙烯酸酯,尤其好的是 q舉曱基丙烯 酯。該等(甲基)丙烯酸酯系單體可為單獨者, r 種以上混合而成者。 ’、可為將兩 苯乙烯系樹脂中之苯乙烯系單體翠 ,& 兩 J 霄量 % 以 上,較好的疋6質量%〜90質量%,進 双对的疋1 0〜60皙晉 %。 置 若苯乙烯系單體單元之比為3質量。In the technical innovation of Diode's light-emitting diode, a new optical molded body suitable for LED light is desired. SUMMARY OF THE INVENTION An object of the present invention is to provide an optical molded article which has less hygroscopicity than a long light path and which has less loss of light transmittance and is excellent in light resistance. Further, an object of the present invention is to provide a light-emitting plate for a liquid crystal display, or a light-conducting material for use in a t-light, or a light-emitting body which is useful as a light diffusing body, in particular, as an LED as a light source. A light guide plate that is useful as a light guide plate for a display or a light diffuser that is useful for applications such as illumination. The present inventors conducted intensive research on the above-mentioned subjects, and found that styrene obtained by polymerizing styrene monomer having less polymerization inhibitor and less phenylacetylene compound content will be borrowed by 145347.doc 201030027. The optical molded article obtained by molding a resin has low hygroscopicity, low loss of light transmittance in a long optical path, and excellent light resistance, and the optical molded body is in a light guide plate or a light diffuser. It is useful to complete the present invention. The optical molding system of the present invention is obtained by molding a styrene-based resin obtained by polymerizing a styrene monomer having a polymerization inhibitor of less than 1 〇 ppm and a acetylene-based compound of ppm or less. The optical molded article of the present invention, in particular, the light guide plate and the light diffuser have low hygroscopicity, are less warped or have small dimensional changes, have less loss of light transmittance in a long optical path, and have good light resistance. Further, the light diffusing body has a good total light transmittance or diffusivity. [Embodiment] <Description of Terms> In the specification of the present application, the symbols "~" refer to "above" and "below". For example, the description of "A to B" means A or more and B or less. In the present specification, the term "molded article for optics" is used for, for example, optical applications such as a light guide plate, a diffusion plate, and a lens. Further, in the present specification, the term "(meth)acrylate monomer" is a generic term for acrylate monomers and mercaptoacrylate monomers. In the present specification, the term "light diffuser" means a person who diffuses light as represented by a diffusion plate or a diffusion cover and emits light on a plane or a curved surface. Hereinafter, embodiments of the optical molded article of the present invention, in particular, a light guide plate 145347.doc 201030027 and a light diffuser will be described in detail. The optical molding system of the present embodiment is formed by molding a styrene resin obtained by polymerizing a styrene-based green body having a polymerization inhibitor of less than 10 ppm and a phenylacetylene compound of 5 〇 ppm or less. By. The optical molded article having the above configuration has less hygroscopicity, less distortion or dimensional change, less loss of light transmittance in a long optical path, and good light resistance. Moreover, the total light transmittance or diffusivity of the light diffuser is also good. [Styrene resin] A stupid vinyl resin is a polymer obtained by polymerizing a styrene monomer. Examples of the styrene-based monomer include styrene, α-methyl styrene, p-methyl styrene, o-methyl styrene, m-methyl styrene, ethyl styrene, p-tert-butyl phenyl b. Rare, preferably styrene. These styrene monomers may be used singly or in combination of two or more. The styrene resin may be a copolymer of a styrene monomer and a monomer copolymerizable with the styrene monomer, and it is preferred to carry out the styrene monomer and the (meth) acrylate monomer. A styrene-(mercapto) acrylate copolymer copolymerized. The styrene-based resin is a styrene-based (meth)acrylic acid vinegar-based copolymer, whereby an effect of good light resistance can be obtained. Examples of the (meth)acrylic acid vinegar-based monomer include (meth)acrylic acid methyl vinegar, (methyl) acrylic acid vinegar, (meth) acrylic acid butyl vinegar, and (methyl) Acrylic acid 2-ethylhexyl vinegar methacrylate vinegar 'acrylic acid methyl vinegar, acrylic vinegar, 145347.doc 201030027 n-butyl propionate, 2-methylhexyl acrylate, π ping acid 2-ethylhexyl Acrylates such as esters and decyl acrylates, and particularly preferred are decyl acrylates. These (meth) acrylate type monomers may be used alone or in combination of two or more. ', may be a styrene-based monomer in the two styrene-based resins, & two J 霄% or more, preferably 疋 6% by mass to 90% by mass, into a double pair of 疋1 0~60皙Jin%. The ratio of the styrene monomer unit is 3 mass.

貝里/〇以上,則光學用成 形體之吸濕性下降’熱穩定性變良好 右本乙烯系單體單 元之比為6質量%〜90質量%,貝,!不僅t學用成形體之吸濕 性下降,熱穩定性變良好,而且可獲得長光程之光透射: 之損耗較少的效果。 系單體單元之比 量% ’進而較好 又,苯乙烯系樹脂中之(甲基)丙烯酸酯 為97質量%以下,較好的是丨〇質量%〜94質 的是40質量%〜90質量%。 若(甲基)丙烯酸醋系單體單元之比為97質量%以下,則 光學用成形體之吸濕性變低,熱穩定性變良好。若(曱基) 丙稀酸醋系單體單元之比為1〇質量%〜94質量%,則不僅; 學用成形體之吸驗下降,熱穩定性變良好,而且可獲得 長光程之光透射率之損耗較少的效果。 苯乙烯系樹脂視需要亦可為苯乙烯系單體與可與苯乙烯 系單體共聚合之乙稀系不飽和單體的共聚物作為上述乙 烯系不飽和單體’例如可列舉丙烯腈、(甲基)丙烯酸、(甲 基)丙烯酸鹽、順丁稀二酸酐等。於使導妓之财熱性提 145347.doc 201030027 高之情形時’較好的是曱基丙烯酸或順丁烯二酸酐。乙烯 系不飽和單體亦可為將兩種以上混合而成者。 此處,苯乙烯系樹脂中之乙烯系不飽和單體單元之比為 35質量%以下’較好的是25質量%以下,進而較好的是2〇 質量%以下。 若乙稀系不飽和單體單元之比為3 5質量。/〇以下,則可獲 付於不失去作為苯乙烯系樹脂之特徵的低吸濕性或成形加 工性之情況下可提高耐熱性等之效果。 (本乙稀系樹脂之分子量) 作為苯乙烯系樹脂之分子量,較好的是利用Gpc(Gei Penneation Chromatography,凝膠滲透層析法)測定之聚苯 乙烯換算之重量平均分子量]^你為7〜45萬分子量分布(重 量平均分子數量平均分子量_)較好的是丨7〜2 3。 若Mw為7萬以上,則可獲得較強固之成形體,若_為 45萬以下’則射出成形時之加工性變良好。又,若斷綠 為1.7以上,則擠出成形時之加工性變良好,若Mw/M“ 2.3以下,則可獲得較強固之成形體。再者, I藉由聚合時之溫度或聚合起始劑量等進行調整。 (苯乙稀系樹脂之光彈性係數) 苯乙稀系樹月旨之A彈性係數較好的是_6xi〇.12〜6xi〇-12/pa 。進而較好的是-4xl〇-12 〜 於光 5?·性係數為-6xl〇-12 〜6χιγρ12/τ» ι± 6χ10 2/Pa之情形時,於製成 導光板時亮度不均變少而較好。 J权野。再者’光彈性係數可藉由 聚合時之可與苯乙烯系單體丑 取合的單體之比例進行調 145347.doc 201030027 整。 (苯乙烯系樹脂之熔體質量流率) 苯乙烯系樹脂之熔體質量流率(MFR,Melt mass-flow rate ’其係根據jis K7210於溫度為200°C、荷重為49 N之 條件下測定者)較好的是0.5〜30 g/1〇分鐘,進而較好的是 3〜20 g/ΙΟ分鐘。When the content of the fiber is more than or equal to the above, the moisture absorption of the molded article for optics is lowered, and the thermal stability is improved. The ratio of the right vinyl monomer unit is from 6% by mass to 90% by mass, which is not only the shape of the molded body. The hygroscopicity is lowered, the thermal stability is improved, and the light transmission of the long path length is obtained: the effect of the loss is small. The amount % of the monomer unit is further preferably, and the (meth) acrylate in the styrene resin is 97% by mass or less, preferably 丨〇% by mass to 94% by mass of 40% by mass to 90%. quality%. When the ratio of the (meth)acrylic acid-based monomer unit is 97% by mass or less, the optical molded article has low hygroscopicity and excellent thermal stability. If the ratio of the (mercapto) acrylic acid vine monomer unit is from 1% by mass to 94% by mass, not only the absorption of the shaped body is lowered, the thermal stability is improved, and the light transmission of the long path is obtained. The effect of less loss of rate. The styrene-based resin may be a copolymer of a styrene-based monomer and an ethylenically unsaturated monomer copolymerizable with a styrene-based monomer, as the above-mentioned ethylenically unsaturated monomer, and examples thereof include acrylonitrile. (Meth)acrylic acid, (meth)acrylic acid salt, cis-succinic acid anhydride, and the like. In the case where the heat of the guide is raised to 145347.doc 201030027, it is preferable that mercaptoacrylic acid or maleic anhydride is used. The ethylenically unsaturated monomer may be a mixture of two or more kinds. Here, the ratio of the ethylenically unsaturated monomer unit in the styrene resin is 35 mass% or less, preferably 25% by mass or less, and more preferably 2% by mass or less. If the ratio of ethylenically unsaturated monomer units is 35 mass. In the case of the following, it is possible to improve the heat resistance and the like without losing the low moisture absorption property or the moldability as a characteristic of the styrene resin. (Molecular weight of the ethylenic resin) The molecular weight of the styrene resin is preferably a polystyrene-equivalent weight average molecular weight measured by Gpc (Gei Penneation Chromatography). The molecular weight distribution of ~45 million (weight average molecular number average molecular weight _) is preferably 丨7~2 3 . When Mw is 70,000 or more, a relatively strong molded body can be obtained, and if _ is 450,000 or less, the workability at the time of injection molding becomes good. In addition, when the green color is 1.7 or more, the workability at the time of extrusion molding is improved, and when Mw/M is 2.3 or less, a relatively strong molded body can be obtained. Further, I is caused by temperature or polymerization at the time of polymerization. The initial dose is adjusted. (The photoelastic coefficient of the styrene resin) The A coefficient of elasticity of the styrene tree is preferably _6xi〇.12~6xi〇-12/pa. Further preferably -4xl〇-12 ~Yuguang 5?· When the coefficient of elasticity is -6xl〇-12 ~6χιγρ12/τ» ι± 6χ10 2/Pa, it is better to reduce the unevenness of brightness when making the light guide plate. Quanye. In addition, the photoelastic coefficient can be adjusted by the ratio of the monomer which can be ugly combined with the styrene monomer during polymerization. 145347.doc 201030027. (Melting mass flow rate of styrene resin) The melt mass flow rate (MFR, Melt mass-flow rate ' of the styrene resin is preferably 0.5 to 30 g/ measured according to jis K7210 at a temperature of 200 ° C and a load of 49 N). 1 minute, and further preferably 3 to 20 g/min.

若MFR為0.5 g/Ι 〇分鐘以上,則射出成形性良好,若 MFR為30 g/l〇分鐘以下,則擠出成形性良好,因而較佳。 MFR可藉由分子量、可與苯乙烯系單體共聚合之單體的種 類或I合時其之比例而進行調整D (苯乙稀系樹脂之形狀) 苯乙烯系樹脂之形狀較好的是顆粒形狀。顆粒化之方法 可採用公知之方法,並無特別限定,例如係藉由如下方式 而獲得:自模嘴熔融擠出直握為2〜5随之股線,進而將 通過冷卻水槽而冷卻之股線切割為長度2〜4酿。 此處’顆粒物中所含之碎粉較好的是未達300 ppm,進 而較好的是1〜。若碎粉未達3〇〇剛,則於長光程 中之先透射率變高。再者,就製造製程方面而t,大多情 況下於顆粒物中含有lppnm上之碎粉。 再者’碎粉例如可藉由如 (Tyler)20網目之金屬筛網 工》’ .使用泰勒 目之金屬師網,將苯乙烯系樹脂100 g篩分5分 鐘,對此時通過金屬網之边 Μ金屬網之碎粉量進行計量。碎粉量 股線切割條件或分級等進行調整。 苯乙烯系樹脂中殘存之 早體與岭劑之合計量較好的是未 145347.doc 201030027 達1000 ppm,進而較好的是1G〜議ppm。再者,就製造製 °大多情況下苯乙烯系樹脂中殘存之單體與溶 劑之含量為1 〇 ppm以上。 於苯乙烯系樹脂中殘存之單體與溶劑之合計量未達1〇〇〇 ppm之情形時,可減少成形時之臭氣或長期使用下之變 色。殘存之單體或剩餘溶劑可藉由脫揮時之溫度或壓力 件等進行調整。 ' 苯乙稀系樹脂中之低聚物量並無特別限制,但若為減少 低聚物量而添加大量之聚合起始劑,則長光程之光透射率 會下降,故欠佳。 於苯乙烯系樹脂中,相對於100質量份之苯乙烯系樹 脂,可添加未達(K5質量份之公知之抗氧化劑耐光穩定 劑、潤滑劑、增塑劑、抗靜電劑,但尤其於導光板之情= 時,較好的是不添加。若上述添加劑未達〇5質量份,則 長光程之光透射率之下降較少。 [聚合抑制劑] 本實施形態之光學用成形體之特徵在於:苯乙烯系單體 中之聚合抑制劑之含量未達10 ppm。藉由使聚合抑制劑未 達10 ppm’於長光程中之光透射率變高,且耐光性變良 好。 又’聚合抑制劑之含量較好的是未達5 ppm,進而較好 的是未達1 ppm。藉由使聚合抑制劑之含量未達5 ppm,可 進一步獲得於長光程中之光透射率變高、且耐光性變良好 之效果。 145347.doc •10- 201030027 作為聚合抑制劑,可列舉對苯二賴或鄰苯二_等。 通常’於可自市場上購入之苯乙稀系單體中含有ι〇〜3〇 ppm左右之聚合抑制劑,故必須將其去除或減少。作為去 除或減v之方法,並無特別限制,可採用蒸餾或吸附等公 头之方法。作為該方法,較好的是減壓蒸餾。 再者,於將可與苯乙烯系單體共聚合之單體進行共聚合 之情形時’較好的是將可與苯乙埽系單體共聚合之單體中 之聚合抑制劑亦分別設為未達10 ppm。 [苯基乙炔系化合物] 本實施开> 態之光學用成形體之特徵在於:苯乙烯系單體 中之苯基乙炔系化合物之含量為50 ppm以下。藉由將苯基 乙炔系化合物設為50 ppm以下,於長光程中之光透射率變 高’且耐光性變良好。 苯基乙炔系化合物之含量較好的是未達40 Ppm,進而較 好的是未達20 ppm。藉由使苯基乙炔系化合物之含量未達 40 ppm,可進一步獲得於長光程中之光透射率變高、且耐 光性變良好之效果。 通常,因苯乙烯中之苯基乙炔之沸點相近而難以將其分 離’故可自市場上購入之苯乙烯令含有15〇 ρρηι左右之苯 基乙炔’而必須將苯基乙块去除或減少。作為去除或減少 之方法,並無特別限制,可採用氫化處理或吸附等公知之 方法。作為該方法,較好的是於氫化觸媒之存在下進行之 氫化處理。 [聚合反應] 145347.doc -11 - 201030027 本實施形態之光學用成形體中使用之苯乙烯系樹脂於聚 合反應中亦尤其好的是藉由溶液聚合而獲得。 作為溶液聚合之溶劑,可使用公知之溶劑,例如甲苯、 二甲苯、乙基苯、己烷、環己烷、丙酮、甲基乙基酮、甲 基異丁基酮等。 相對於所使用之單體之合計100質量份,溶劑之使用量 較好的是1〜70質量份,進而較好的是2〜3〇質量份。 若相對於所使用之單體之合計100質量份,溶劑之使用 量為1〜70質量份,則不僅容易藉由溶液聚合而控制聚合時❺ 之黏度,而且於進行共聚合之情形時,共聚合組成分布變 窄’長光程之光透射率之損耗變少。 又,作為聚合反應,尤其好的是自由基溶液聚合。自由 基溶液聚合與陰離子聚合或陽離子聚合、配位聚合相比, 苯乙烯系樹脂中殘存之起始劑或助劑之影響較少,長光程 之光透射率或耐光性較高。 (聚合起始劑) 於自由基聚合時,作為自由基產生源,可添加有機過氧❹ 化物或偶氮化合物等公知之聚合起始劑。 作為聚合起始劑,較好的是1小時半生期溫度為 95 140 C、奪氫能力較低、不含苯環者。奪氫能力較低者 不易產生微小之凝膠成分,故長光程之光透射率之損耗變 ^又,不含苯環者不易生成著色成分,因而長光程之光 透射率之損耗變少。 作為聚合起始劑之較佳例,可列舉U1_:(第三己基過氧 145347.doc •12· 201030027 基)-3,3,5-三甲基環己貌、ι 烧、過乳化異丙基單碳酸第 等0 二(第三己基過氧基)-環己 —•己S旨 '過氧化一第三己基 又,相對於單體之人斗〗# °计100質量份,聚合起始劑之添加 量較好的是0.01〜0.5質量份。决 置物 進而較好的是0.02〜〇·2質量 份。若聚合起始劑之承‘县:^。 剛之添加量為〇.01〜〇 5質量份,則長光程 之光透射率及耐光性變良好。 (鏈轉移劑)When the MFR is 0.5 g/Ι 〇 or more, the injection moldability is good, and when the MFR is 30 g/l 〇 or less, the extrusion moldability is good, which is preferable. The MFR can be adjusted by the molecular weight, the type of the monomer copolymerizable with the styrene monomer, or the ratio of the I when it is combined. D (The shape of the styrene resin) The shape of the styrene resin is preferably Particle shape. The method of granulating can be carried out by a known method, and is not particularly limited, and is obtained, for example, by melt-extrusion from a nozzle, a straight grip of 2 to 5, followed by a strand, and then a strand cooled by a cooling water tank. Wire cuts are brewed for lengths of 2 to 4. Here, the fine powder contained in the granules is preferably less than 300 ppm, and more preferably 1 〜. If the powder is less than 3 inches, the transmittance will increase first in the long path. Further, in terms of the manufacturing process, t, in many cases, the powder in the granules contains lppnm. Furthermore, the 'powder powder can be sieved by a metal mesh such as (Tyler) 20 mesh.') The styrene resin 100 g is sieved for 5 minutes using a metal mesh of Tyler. The amount of broken powder of the side metal mesh is measured. The amount of broken powder is adjusted by the cutting condition or classification of the strands. The total amount of the early body and the ridge agent remaining in the styrene resin is preferably 145347.doc 201030027 up to 1000 ppm, and more preferably 1 G to ppm. Further, in the case of the production process, the content of the monomer and the solvent remaining in the styrene resin is often 1 〇 ppm or more. When the total amount of the monomer and the solvent remaining in the styrene resin is less than 1 〇〇〇 ppm, the odor at the time of molding or the color change under long-term use can be reduced. The remaining monomer or residual solvent can be adjusted by temperature or pressure during devolatilization. The amount of the oligomer in the styrene-based resin is not particularly limited. However, if a large amount of a polymerization initiator is added to reduce the amount of the oligomer, the light transmittance of the long path is lowered, which is not preferable. In the styrene-based resin, less than (K 5 parts by mass of a known antioxidant light stabilizer, a lubricant, a plasticizer, and an antistatic agent may be added to 100 parts by mass of the styrene resin, but especially In the case of the light plate, it is preferable that it is not added. If the additive is less than 5 parts by mass, the light transmittance of the long path is less decreased. [Polymerization inhibitor] The optical molded body of the present embodiment is characterized by The content of the polymerization inhibitor in the styrene monomer is less than 10 ppm. By making the polymerization inhibitor less than 10 ppm', the light transmittance in the long light path becomes high, and the light resistance becomes good. The content is preferably less than 5 ppm, and more preferably less than 1 ppm. By making the polymerization inhibitor content less than 5 ppm, the light transmittance in the long optical path is further improved, and the light resistance is improved. 145347.doc •10- 201030027 As a polymerization inhibitor, p-benzoic acid or o-phenylene ruthenium or the like can be cited. Usually, styrene monomer which is commercially available from the market contains ι〇~ a polymerization inhibitor of about 3 〇 ppm, so It is necessary to remove or reduce it. The method of removing or subtracting v is not particularly limited, and a method such as distillation or adsorption may be employed. As the method, distillation under reduced pressure is preferred. In the case where the monomer in which the styrene monomer is copolymerized is copolymerized, it is preferred that the polymerization inhibitor in the monomer copolymerizable with the styrene monomer is also set to less than 10 ppm, respectively. Phenylacetylene-based compound The optical molded article of the present invention is characterized in that the content of the phenylacetylene compound in the styrene monomer is 50 ppm or less. Below 50 ppm, the light transmittance in the long pathlength becomes high and the light resistance becomes good. The content of the phenylacetylene compound is preferably less than 40 Ppm, and more preferably less than 20 ppm. The content of the acetylene-based compound is less than 40 ppm, and the light transmittance in the long optical path is further increased, and the light resistance is improved. Generally, it is difficult to separate the phenylacetylene in styrene because the boiling points thereof are similar. 'It can be purchased from the market The styrene is required to contain or reduce the phenylacetylene of about 15 〇ρρηι. The method of removing or reducing is not particularly limited, and a known method such as hydrogenation treatment or adsorption may be employed. The method is preferably a hydrogenation treatment in the presence of a hydrogenation catalyst. [Polymerization reaction] 145347.doc -11 - 201030027 The styrene resin used in the optical molded article of the present embodiment is also particularly preferable in the polymerization reaction. It is preferably obtained by solution polymerization. As the solvent for solution polymerization, a known solvent such as toluene, xylene, ethylbenzene, hexane, cyclohexane, acetone, methyl ethyl ketone or methyl isophthalate can be used. Butyl ketone and the like. The solvent is preferably used in an amount of from 1 to 70 parts by mass, more preferably from 2 to 3 parts by mass, per 100 parts by mass of the total of the monomers to be used. When the solvent is used in an amount of from 1 to 70 parts by mass based on 100 parts by mass of the total of the monomers to be used, it is not only easy to control the viscosity of the ruthenium during polymerization by solution polymerization, but also in the case of copolymerization. The distribution of the polymerization composition is narrowed, and the loss of the light transmittance of the long path is reduced. Further, as the polymerization reaction, particularly preferred is a radical solution polymerization. The free radical solution polymerization has less influence on the residual initiator or auxiliary agent remaining in the styrene resin than the anionic polymerization or cationic polymerization or coordination polymerization, and the light transmittance or light resistance of the long optical path is high. (Polymerization Initiator) In the case of radical polymerization, a known polymerization initiator such as an organic peroxyhalide compound or an azo compound may be added as a source of radical generation. As the polymerization initiator, it is preferred that the one-hour half-life temperature is 95 140 C, the hydrogen abstraction ability is low, and the benzene ring is not contained. Those with lower hydrogen scavenging ability are less likely to produce tiny gel components, so the loss of light transmittance of long optical paths becomes smaller, and those that do not contain benzene rings are less likely to generate colored components, and thus the loss of light transmittance of long optical paths is reduced. Preferred examples of the polymerization initiator include U1_: (third hexylperoxy 145347.doc •12·201030027 base)-3,3,5-trimethylcyclohexene, iota, over-emulsified isopropyl The mono-carbonic acid is equivalent to 0 (the third hexylperoxy)-cyclohexan---the s-there is a peroxidation-third hexyl group, and the monomer is compared with the monomer. The amount of the agent added is preferably from 0.01 to 0.5 parts by mass. The composition is further preferably 0.02 to 2 parts by mass. If the polymerization initiator is in the ‘County: ^. When the amount of addition is 〇.01 to 〇 5 parts by mass, the light transmittance and light resistance of the long optical path become good. (chain transfer agent)

又,於自由基聚合時 二-十 '一烧基硫醇或2,4_ 轉移劑。 ’亦可添加正十二烷基硫醇、第 二苯基-4-甲基-1-戊烯等公知之鏈 相對於單體之合計1G〇f量份,鍵轉移劑之添加量較好 的疋0.001 0.5質量份’進而較好的是〇 〇〇5〜〇 2質量份。 若鍵轉移劑之添加量為0.001〜0.5質歸,則於長光程中之 光透射率變高,且耐光性變良好。Further, in the case of radical polymerization, di-ten'-alkyl mercaptan or 2,4_ transfer agent. 'It is also possible to add a total amount of 1G〇f of a known chain such as n-dodecyl mercaptan or second phenyl-4-methyl-1-pentene to the monomer, and the amount of the bond transfer agent is preferably added.疋 0.001 0.5 parts by mass 'and more preferably 〇〇〇 5 〇 2 parts by mass. When the amount of the bond transfer agent added is 0.001 to 0.5, the light transmittance in the long light path is increased, and the light resistance is improved.

苯乙烯系樹脂之聚合時之聚合溫度較好的是9〇〜i8(rc, 進而較好的是95〜17(rC。若聚合溫度為90〜18(rc,則長光 程之光透射率及耐光性變良好。 (溶氧之去除) 本實施形態之光學用成形體中使用之苯乙烯系單體及溶 劑較好的是於去除溶氧之後供於聚合。作為去除溶氧之方 法,並無特別限制,可採用使用氮氣進行起泡處理之方法 等。 若去除溶氧,則有成形體之顏色為無色而對於光學用途 I45347.doc •13- 201030027 變良好之情形。再者,於將可與苯乙烯系單體共聚合之單 體進行共聚合之情形時,較好的是將可與笨乙烯系單體共 聚合之單體的溶氧亦去除之後供於聚合。 (異物之去除) 又’本實施形態之光學用成形體中使用之苯乙稀系單體 及溶劑較好的是去除異物之後供於聚合。作為去除異物之 方法,並無特別限制,可採用藉由過濾器進行過濾之方法 等。 若去除異物’則有長光程之光透射率變高之情形。再 者’於將可與苯乙烯系單體共聚合之單體進行共聚合之情 形時,較好的是將可與苯乙烯系樹脂共聚合之單體的異物 亦去除之後供於聚合。 對於本實施形態之苯乙烯系樹脂而言,可利用射出成形 法、擠出成形法、溶劑澆鑄法等公知之方法將苯乙烯系樹 脂成形而製成光學用成形體。尤其好的是射出成形法或擠 出成形法。 對於成形條件,並無特別限制,較好的是於200〜30(rc 下成形。 [導光板] 作為本實施形態之光學用成形體之用途,可列舉導光 板、擴散板、透鏡等。尤其,本實施形態之光學用成形體 因於長光程中之光透射率之損耗較少、且尤其對於4〇〇 nm 以上之波長的光之耐光性良好,故作為液晶顯示器用之導 光板或照明用之導光板較為有用,尤其是作為以LED為光 145347.doc -14. 201030027 源之中〜大型液晶顯示器用之導光板較為有 本實施形態之導光板之厚度較好的是〇3 用0 〜8 mm,進而較 好的是0·4〜5關。具有上述厚度之導光板可作為射以上 之中〜大型顯示器用之導光板而充分導入光又,於操作 上具有充分剛性之方面有效果。The polymerization temperature at the time of polymerization of the styrene resin is preferably 9 〇 to i8 (rc, more preferably 95 to 17 (rC. If the polymerization temperature is 90 to 18 (rc, the light transmittance of the long pathlength and the light resistance) (The removal of dissolved oxygen) The styrene monomer and the solvent used in the optical molded article of the present embodiment are preferably subjected to polymerization after removing dissolved oxygen. As a method of removing dissolved oxygen, there is no In particular, a method of performing a foaming treatment using nitrogen gas or the like can be employed. If the dissolved oxygen is removed, the color of the molded body is colorless and the optical use is good for I45347.doc •13-201030027. In the case where the monomer copolymerized with the styrene monomer is copolymerized, it is preferred that the dissolved oxygen of the monomer copolymerizable with the stupid vinyl monomer is also removed and then polymerized. (Removal of foreign matter) Further, the styrene monomer and the solvent used in the optical molded article of the present embodiment are preferably subjected to polymerization after removing foreign matter. The method for removing foreign matter is not particularly limited, and may be carried out by a filter. Method of filtering, etc. If the foreign matter is removed, the light transmittance of the long optical path becomes high. In addition, when the monomer copolymerizable with the styrene monomer is copolymerized, it is preferable to be compatible with the styrene system. The styrene-based resin of the present invention can be polymerized by a known method such as an injection molding method, an extrusion molding method, or a solvent casting method. It is formed into an optical molded body, and particularly preferably an injection molding method or an extrusion molding method. The molding conditions are not particularly limited, but it is preferably formed at 200 to 30 (rc). [Light guide plate] The use of the optical molded article of the embodiment includes a light guide plate, a diffusion plate, a lens, etc. In particular, the optical molded article of the present embodiment has less loss of light transmittance in a long optical path, and particularly for 4 〇〇. Since the light having a wavelength of nm or higher has good light resistance, it is useful as a light guide plate for a liquid crystal display or a light guide plate for illumination, especially as a light source of 145347.doc -14. 201030027. The light guide plate for a liquid crystal display device has a thickness of the light guide plate of the present embodiment. Preferably, the thickness of the light guide plate is 0 to 8 mm, and more preferably 0.4 to 5 turns. The light guide plate having the above thickness can be used as the light guide plate. Among the above, it is effective to introduce sufficient light into the light guide plate for a large display, and to have sufficient rigidity in operation.

於本實施形態之導光板中,可於不損及本實施形態之目 的之範圍内,調配作為其他成分之交聯丙烯酸系粒子、交 聯苯乙稀系粒子、魏烧樹脂粒子等有機系光擴散劑,硫 酸锅、碳酸鈣、氧化鈦等無機系光擴散劑。 [光擴散體] 又,於本實施形態之光學用成形體之用途為光擴散體之 情形時,亦成為全光線透射率(或者光透射率)或擴散率等 光學物性變良好。因此,可使用作為照明等各種用途中使 用之光擴散體。 作為用作光擴散體而使光擴散之方法,可採用混練光擴 散劑之方法或利用對表面賦形之方法、將光擴散劑塗佈於 表面之方法等各種方法。 作為光擴散劑,可使用交聯丙烯酸系粒子、交聯苯乙烯 系粒子石夕氧院樹脂粒子等有機系光擴散劑,硫酸鋇、碳 酸約、氧化鈦等無機系光擴散劑。於將交聯丙稀酸系粒子 或父聯笨乙烯系粒子、石夕氧烧樹脂粒子、碳酸鈣製成光擴 散體時’全光線透射率或擴散率等光學物性之平衡良好, 故較佳。 光擴散體中之光擴散劑之含量並無特別限制,若以〇 145347.doc •15· 201030027 質量/〇以上、10質量y〇以下之範圍而含有則可獲得全光 線透射率與擴散率各自優異或者兩者之平衡優異的光擴散 體。藉由含有0.1質量%以上之光擴散劑,可具有較高之擴 散性能,藉由設為1〇質量%以下,全光線透射率之下降較 少〇 作為使光擴散體中含有光擴散劑之方法,可採用擠出成 形等公知之方法。 於本實施形態之光擴散體中,相對於1〇〇質量份之苯乙 烯系樹脂,可添加未達0.5質量份之公知之抗氧化劑、耐 光穩定劑、潤滑劑、增塑劑、抗靜電劑、螢光增白劑、螢 光材料、蓄光材料。若上述添加劑未達〇.5質量份,則全 光線透射率(或者光透射率)或擴散率等光學物性之了降較 /J、。 <作用效果> 以下,就上述實施形態之光學用成形體、尤其是導光板 及光擴散體之作用效果加以說明。 上述實施形態之光學用成形體係將藉由使聚合抑制劑未 達10 ppm、且苯基乙炔系化合物為50 ppm以下之苯乙稀系 單體進行聚合反應所得之苯乙烯系樹脂成形而成者。 上述實施形態之光學用成形體由於吸濕性較低故勉曲或 尺寸變化較少,於長光程中之光透射率之損耗較少,且耐 光性良好。 尤其’藉由使上述本乙烯系樹脂為苯乙婦_(甲基)丙烯酸 酯系共聚物,可獲得翹曲或尺寸變化、於長光程中之光透 145347.doc 201030027 射率、耐光性之平衡更良好之效果。 又,藉由使上述聚合反應為自由基溶液聚合反應,可獲 得苯乙稀系樹脂中殘存之起始劑或助劑之影響較少、長光 程之光透射率或耐光性變高之效果。In the light guide plate of the present embodiment, organic light such as crosslinked acrylic particles, crosslinked styrene particles, or Wei resin particles can be blended as other components within the range not impairing the object of the present embodiment. A diffusing agent, an inorganic light diffusing agent such as a sulfuric acid pot, calcium carbonate or titanium oxide. [Light-diffusing body] When the use of the optical molded article of the present embodiment is a light-diffusing body, the optical properties such as total light transmittance (or light transmittance) and diffusivity are also improved. Therefore, a light diffuser used for various purposes such as illumination can be used. As a method of diffusing light as a light-diffusing body, various methods such as a method of kneading a light-diffusing agent, a method of forming a surface, and a method of applying a light-diffusing agent to a surface can be employed. As the light-diffusing agent, an organic light diffusing agent such as crosslinked acrylic particles, crosslinked styrene-based particles, or a ceramic light diffusing agent such as barium sulfate, carbonic acid or titanium oxide can be used. When the cross-linked acrylic acid particles, the parent-linked vinyl-based particles, the asahicin-fired resin particles, and the calcium carbonate are used as a light-diffusing body, the balance of optical properties such as total light transmittance and diffusivity is good, so that it is preferable. . The content of the light diffusing agent in the light diffuser is not particularly limited, and if it is contained in the range of 〇145347.doc •15·201030027 mass/〇 or more and 10 mass y〇 or less, the total light transmittance and the diffusivity are respectively obtained. A light diffuser that is excellent or has a good balance between the two. By containing 0.1% by mass or more of the light diffusing agent, it is possible to have a high diffusing property, and by setting it as 1% by mass or less, the total light transmittance is less reduced as the light diffusing body contains the light diffusing agent. As the method, a known method such as extrusion molding can be employed. In the light-diffusing body of the present embodiment, less than 0.5 part by mass of a known antioxidant, a light stabilizer, a lubricant, a plasticizer, and an antistatic agent may be added to 1 part by mass of the styrene resin. , fluorescent brightener, fluorescent material, light storage material. When the above additive is less than 5 parts by mass, the optical properties such as total light transmittance (or light transmittance) or diffusivity are lowered by /J. <Operation and Effect> The effects of the optical molded article of the above embodiment, in particular, the light guide plate and the light diffuser will be described. The optical molding system of the above-described embodiment is formed by molding a styrene resin obtained by polymerizing a styrene monomer having a polymerization inhibitor of less than 10 ppm and a phenylacetylene compound of 50 ppm or less. . Since the optical molded article of the above embodiment has low hygroscopicity, it has little distortion or dimensional change, and the loss of light transmittance in a long optical path is small, and the light resistance is good. In particular, by making the above-mentioned ethylene-based resin a styrene-(meth)acrylate-based copolymer, warpage or dimensional change and light transmission in a long optical path can be obtained. 145347.doc 201030027 Balance of light transmittance and light resistance Better results. Further, by subjecting the polymerization reaction to a radical solution polymerization reaction, the effect of reducing the amount of the initiator or the auxiliary agent remaining in the styrene-based resin and increasing the light transmittance or light resistance of the long path can be obtained.

上述實施形態之光學用成形體因於長光程中之光透射率 之扣耗較少、且尤其對於4〇〇 nm以上之波長的光之耐光性 良好,故作為液晶顯示器用之導光板或照明用之導光板較 為有用’尤其是作為以LED為光源之中〜大型液晶顯示器 用之導光板較為有用。 又’上述實施形態之光學用成形體係全光線透射率(或 者光透射率)或擴散率等光學物性亦變良好。因此,作為 照明等各種用途中使用之光擴散體較為有用。 以上,列舉實施形態對本發明之光學用成形體、尤其是 導光板及光擴散體進行了說明,但本發明並不限定於該等 實施形態。 例如本發明之光學用成形體由於翹曲或尺寸變化較 少’故不僅可較好地用於中〜大型顯示器,而且亦可較好 地用於要求精密尺相整之小型顯示器^進而,亦可較好 地用於顯示器以外之照明器具或顯示器具用途。 本發月之光學用成形體亦可藉由包括以下步驟之製 造方法獲得。 光予用成形體之製造方法,其包括:準備苯乙烯系單體 之步驟;將苯乙稀系單體中所含之聚合抑制劍減少至未達 1 PPm之步驟’將苯乙烯系單體中所含之苯基乙炔系化合 145347.doc 201030027 物減少至50 ppm以下之步驟;使苯乙烯系單體進行聚合反 應而獲得苯乙烯系樹脂之聚合反應步驟;以及將苯乙烯系 樹脂成形之成形步驟。 藉由上述製造方法獲得之光學用成形體由於吸濕性較低 故翹曲或尺寸變化較少,於長光程中之光透射率之損耗較 少,且耐光性良好。 [實施例] 以下,使用實施例就本發明之光學用成形體、尤其是導 光板及光擴散體之詳細内容加以說明,但本發明並不限定 於以下實施例。 [苯乙烯系單體] 首先,就實施例及比較例中使用之苯乙烯系單體加以說 明。 (苯乙烯-1) 準備工業苯乙烯,結果得知其含有12 ppm之作為聚合抑 制劑的4-第三丁基鄰苯二酚、及130 ppm之作為雜質的苯 基乙炔。將該工業苯乙烯於氫化觸媒之存在下進行氫化處 理,而選擇性地氫化所含之苯基乙炔,其後進行減壓蒸 館,而獲得4 -第二丁基鄰苯.一盼含夏未達0.1 ppm、且苯基 乙快含量為10 ppm之苯乙稀-1。 (苯乙烯-2) 於苯乙稀-1中添加4-第三丁基鄰苯二紛,而獲得4 -第三 丁基鄰苯二酚之含量為7 ppm之苯乙烯-2。 (苯乙烯·3) 145347.doc -18- 201030027 於苯乙烯-1中添加4-第三丁基鄰苯二紛,而獲得心第三 丁基鄰苯二酚之含量為12 ppm之苯乙稀_3。 (苯乙烯-4) 於苯乙烯-1中添加苯基乙炔,而獲得笨基乙块之含量為 43 ppm之苯乙稀-4。 (苯乙烯-5) 於苯乙烯-1中添加苯基乙炔,而獲得苯基乙炔之含量為 130 ppm之苯乙烯-5。 ® [(甲基)丙烯酸酯系單體] (MMA-1) 其次’就(甲基)丙烯酸酯系單體加以說明。 準備工業甲基丙烯酸甲酯,結果得知其含有5 ppm之作 為聚合抑制劑的Topano卜將其作為μμα」。 [實施例1] 將52質量份之上述苯乙烯、48質量份之上述mma_卜 參 12質量份之作為溶劑之乙苯進行混合,使用氮氣進行^】、 時起泡而去除溶氧之後,利用1 0瓜之過濾器過濾上清液, 製成原料溶液。 繼而,將附有攪拌機之容積為約5公升之第一完全混合 型反應器、容積為約15公升之第二完全混合型反應器、容 積為約40公升之塔式活塞流型反應器、及附有預熱器之脫 揮槽串列連接而構成。 於原料溶液中混合0.03質量份之1,1_二(第三己基過氧 化)-¾己院(日本油脂公司製造之perhexa HC)、及0.015質 145347.doc •19- 201030027 量伤之正十—烧基硫醇(花王公司製造之叫, 並以每小時6 kg而導入至將溫度控制為价之第一完全混 合型反應器内。 再者’於第-完全混合型反應器之攪拌機之旋轉速度為 3〇0啊下實施反應。自第—完全混合型反應器中連續抽 取反應液,並導人至將溫度㈣為125。€之第二完全混合 型反應器内。 又,於第二完全混合型反應器之授拌機之旋轉速度為 刚—下實施反應。自第二完全混合型反應器中連續抽 取反應液,並導入至以朝向流動方向而賦予125艺至16〇艺 之溫度梯度的方式加以調整的塔式活塞流型反應器内。 一面利用預熱器加溫該反應液,一面將其導入至溫度為 24(rc且將壓力控制為i G kpa之脫揮槽内,而去除溶劑或 未反應單體等揮發成分。 繼而,利用齒輪泵抽取該樹脂液並以股線狀而擠出,一 面冷卻一面進行切割’由此獲得顆粒形狀之笨乙烯系樹 脂。再者’顆粒物令所含之微粉係藉由分級而去除。 對於所獲得之苯乙烯系樹脂,已確認到Mw =丨8萬、 Mw/Mn 18,且苯乙稀系樹脂中殘存之單體與溶劑之合 計量未達1000 ppm,碎粉未達3〇〇 ppm。 再者,碎粉係藉由如下方式計算:使用泰勒2〇網目之金 屬篩網,將苯乙烯系樹脂100 g篩分5分鐘,對此時通過金 屬網之碎粉量進行計量。 藉由電動射出成形機(股)日本製鋼所公司製造之 145347.doc 201030027 J350ELIII於270°C之成形溫度下將顆粒物成形,而獲得縱 向為292.5 mm、橫向為220 mm、厚度為2 mm之成形體。 進行所獲得之成形體之光學特性評價。將其結果示於表 [實施例2] 將苯乙烯-1設為40質量份、MMA-1設為60質量份,除此 以外’以與實施例1相同之方式進行。將其結果示於表j。 [實施例3] 將苯乙烯-1設為11質量份、MMA_丨設為89質量份,除此 以外,以與實施例〗相同之方式進行。將其結果示於表i。 [實施例4] 將苯乙烯-1設為100質量份、MMA-1設為〇質量份,除此 以外,以與實施例1相同之方式進行。將其結果示於幻。 [實施例5] 使用苯乙稀-2來代替苯乙浠q,除此以外,以與實施例 1相同之方式進行。將其結果示於表i。 [實施例6] 使用苯乙烯-4來代替苯乙烯-1,除此以外,以與實施 1相同之方式進行。將其結果示於表i。 再者,上述成形體之特性評價係藉由下述方法進行。 (1)聚合抑制劑(4-第三丁基鄰笨二酚) 分=5氫氧化納並加,拌,對著色之溶跳 二 =測疋吸光度(波長為· nm),並根據預緣 之杈準曲線(standard curve)計算出濃产 145347.doc -21- 201030027 (2) 殘存單體、殘存溶劑、苯基乙炔 於下述記載之GC(Gas Chromatography,氣相層析法)測 定條件下進行測定。 裝置名:島津製作所公司製造之GC12A FID檢測器(flame ionization detector,火焰離子化檢測器) 管柱:玻璃管柱03 mm><3 m 填充劑:聚乙二醇 載氣:氮氣In the optical molded article of the above-described embodiment, since the light transmittance in the long optical path is small, and the light having a wavelength of 4 nm or more is excellent in light resistance, it is used as a light guide plate or illumination for a liquid crystal display. The light guide plate is useful, especially as a light guide plate for a large liquid crystal display. Further, the optical molding system of the above-described embodiment also has excellent optical properties such as total light transmittance (or light transmittance) or diffusivity. Therefore, it is useful as a light diffuser used for various applications such as illumination. In the above, the optical molded article of the present invention, in particular, the light guide plate and the light diffusing body have been described. However, the present invention is not limited to the embodiments. For example, the molded article for optics of the present invention is not only preferably used for medium to large displays due to warpage or dimensional change, but can also be preferably used for small displays requiring precision scales. It can be preferably used for lighting fixtures or display appliances other than displays. The molded article for optics of the present month can also be obtained by a manufacturing method including the following steps. A method for producing a molded article for photo-imaging, comprising: a step of preparing a styrene-based monomer; and a step of reducing a polymerization inhibition sword contained in the styrene-based monomer to less than 1 ppm; a step of reducing the phenylacetylene compound 145347.doc 201030027 to 50 ppm or less; a polymerization reaction step of obtaining a styrene resin by polymerization of a styrene monomer; and forming a styrene resin Forming step. The optical molded article obtained by the above-described production method has less hygroscopicity, less warpage or dimensional change, less loss of light transmittance in a long optical path, and good light resistance. [Examples] Hereinafter, the details of the optical molded article of the present invention, particularly the light guide plate and the light diffuser, will be described using the examples, but the present invention is not limited to the following examples. [Styrene-based monomer] First, the styrene-based monomers used in the examples and comparative examples will be described. (Styrene-1) Industrial styrene was prepared, and as a result, it was found to contain 12 ppm of 4-tert-butyl catechol as a polymerization inhibitor, and 130 ppm of phenylacetylene as an impurity. The industrial styrene is subjected to a hydrogenation treatment in the presence of a hydrogenation catalyst, and the phenylacetylene contained therein is selectively hydrogenated, and then subjected to a vacuum distillation to obtain 4 - 2 butyl phthalic acid. Xia Weida 0.1 ppm, and phenylethyl fast content of 10 ppm of styrene-1. (Styrene-2) 4-Terbutyl phthalic acid was added to styrene-1 to obtain styrene-2 having a content of 4 ppm of butyl catechol of 7 ppm. (styrene·3) 145347.doc -18- 201030027 Add 4-tert-butyl phthalate to styrene-1 to obtain phenylethyl bromide with a content of 12 ppm of butyl catechol Thin _3. (Styrene-4) Phenylacetylene was added to styrene-1 to obtain styrene-4 having a stupid block content of 43 ppm. (Styrene-5) Phenylacetylene was added to styrene-1 to obtain styrene-5 having a phenylacetylene content of 130 ppm. ® [(Meth)acrylate monomer] (MMA-1) Next, the (meth)acrylate monomer will be described. Industrial methyl methacrylate was prepared, and it was found that it contained 5 ppm of Topano as a polymerization inhibitor as μμα. [Example 1] 52 parts by mass of the above-mentioned styrene, 48 parts by mass of the above-mentioned mma-b. 12 parts by mass of ethylbenzene as a solvent were mixed, and nitrogen gas was used for foaming to remove dissolved oxygen. The supernatant was filtered using a 10 melon filter to prepare a raw material solution. Then, a first fully mixed reactor having a volume of about 5 liters, a second fully mixed reactor having a volume of about 15 liters, a tower plug flow reactor having a volume of about 40 liters, and The devolatilizer with the preheater is connected in series. 0.03 parts by mass of 1,1_two (Third Hexyl Peroxide)-3⁄4 hexane (perhexa HC manufactured by Nippon Oil & Fats Co., Ltd.), and 0.015 145347.doc •19-201030027 were mixed in the raw material solution. - a mercaptan thiol (manufactured by Kao Corporation, and introduced at a rate of 6 kg per hour to the first fully mixed reactor where the temperature is controlled to be priced. Further in the mixer of the first-completely mixed reactor) The reaction was carried out at a rotation speed of 3 〇 0. The reaction liquid was continuously withdrawn from the first-completely mixed reactor, and was introduced into a second fully mixed reactor at a temperature (four) of 125 ° C. The rotation speed of the mixer of the two-mixed reactor is the reaction of the first-lower reaction. The reaction liquid is continuously extracted from the second complete-mixing reactor, and is introduced to give 125 art to 16 art in the direction of flow. In the tower plug flow type reactor adjusted by the temperature gradient method, the reaction liquid is heated by a preheater, and is introduced into a devolatilization tank having a temperature of 24 (rc and controlling the pressure to i G kpa). While removing solvent or not reacting The volatile component of the body is then extracted by a gear pump, and extruded in a strand shape, and cut while cooling, thereby obtaining a powdery stupid vinyl resin. Further, the particulate matter is contained in the fine powder system. The styrene resin obtained has been confirmed to have Mw = 丨80,000, Mw/Mn 18, and the total amount of the monomer and solvent remaining in the styrene resin is less than 1000 ppm. The powder was less than 3 ppm. Further, the powder was calculated by using a metal mesh of a Taylor 2 mesh and sieving 100 g of the styrene resin for 5 minutes, at which time it was passed through a metal mesh. The amount of powdered powder was measured. The pellets were formed by a motor injection molding machine (manufactured by Nippon Steel Works, Ltd.) 145347.doc 201030027 J350ELIII at a forming temperature of 270 ° C to obtain a longitudinal direction of 292.5 mm and a lateral direction of 220 mm. A molded article having a thickness of 2 mm. The optical properties of the obtained molded article were evaluated. The results are shown in the table. [Example 2] styrene-1 was 40 parts by mass, and MMA-1 was 60 parts by mass. In addition to 'implementation and implementation The results are shown in the same manner. The results are shown in Table J. [Example 3] The same procedure as in Example 1 except that the styrene-1 was 11 parts by mass and the MMA_丨 was 89 parts by mass. The results are shown in Table 1. [Example 4] The same procedure as in Example 1 was carried out except that styrene-1 was used in an amount of 100 parts by mass and MMA-1 was used as the mass%. The results are shown in the following. [Example 5] The same procedure as in Example 1 was carried out except that styrene-2 was used instead of phenethyl bromide. The results are shown in Table i. [Example 6] The same procedure as in Example 1 was carried out except that styrene-4 was used instead of styrene-1. The results are shown in Table i. Further, the evaluation of the characteristics of the above-mentioned molded body was carried out by the following method. (1) polymerization inhibitor (4-tert-butyl phthalate) = 5 NaOH and added, mixed, the color of the solution hop 2 = measured absorbance (wavelength · nm), and according to the pre-preparation The standard curve is used to calculate the yield 145347.doc -21- 201030027 (2) Residual monomer, residual solvent, and phenylacetylene are determined by GC (Gas Chromatography) as described below. The measurement was carried out. Device name: GC12A FID detector (flame ionization detector) manufactured by Shimadzu Corporation. Column: glass column 03 mm><3 m Filler: polyethylene glycol Carrier gas: nitrogen

溫度:管柱115°C、注入口 220°C 使0.5 g之試料顆粒物、0.001 g之環戊烷、N,N-二曱基甲醯 胺溶解,以環戊烷為内標準進行測定。 (3) 吸濕性 使用所成形之板,根據JIS K7209,利用A法求出飽和吸 水率(單位:%)。將未達1.5%者評價為合格。 (4) Haze(霧度) 對於所成形之板之2 mm厚度部,根據JIS K7 105使用測 霧計(日本電色工業公司製造之NDH2000)測定霧度(單位: %)。將未達0.3%者評價為合格。 (5) 長光路之透明性(光透射率) 使用Megaro Technica(股)公司製造之閘口加工機GCPB 研磨所成形之板之端面。使用日本電色工業(股)公司製造 之長光程測定機ASA-300A,測定垂直透射經研磨之面的 光之透射率(單位:%)。 (6) 折射率 145347.doc -22- 201030027 對於所成形之板之2 mm厚度部,使用阿貝折射計 (Atago(股)公司製造之阿貝折射計2-T)測定折射率。 (7)反射率 利用下式,使用(6)中測定出之折射率計算出反射率(單 位:%)。 [數1] χΙΟΟ 反射率 (1+折射率>2Temperature: column 115 ° C, injection port 220 ° C 0.5 g of sample particles, 0.001 g of cyclopentane, N,N-dimercaptocarbamide were dissolved, and the measurement was carried out using cyclopentane as an internal standard. (3) Hygroscopicity Using the formed plate, the saturated water absorption rate (unit: %) was determined by the A method in accordance with JIS K7209. Those who did not reach 1.5% were evaluated as qualified. (4) Haze (haze) For the 2 mm thickness portion of the formed plate, the haze (unit: %) was measured in accordance with JIS K7 105 using a fog meter (NDH2000 manufactured by Nippon Denshoku Industries Co., Ltd.). Those who did not reach 0.3% were evaluated as qualified. (5) Transparency of light path (light transmittance) The end face of the formed plate was ground using a gate processing machine GCPB manufactured by Megaro Technica Co., Ltd. The transmittance (unit: %) of light transmitted vertically through the polished surface was measured using a long path length measuring machine ASA-300A manufactured by Nippon Denshoku Industries Co., Ltd. (6) Refractive index 145347.doc -22- 201030027 The refractive index was measured using an Abbe refractometer (Abb refractometer 2-T manufactured by Atago Co., Ltd.) at a thickness of 2 mm of the formed plate. (7) Reflectance The reflectance (unit: %) was calculated by the following formula using the refractive index measured in (6). [Number 1] 反射 Reflectance (1+refractive index>2

(8)長光程之透明損耗率 利用下式’使用(5)中測定出之長光程之光透射率與(7) 中計算出之反射率,計算出透明損耗率(單位:%)。再 者’將反射率乘2倍係表示入光面與出光面兩面。將未達 8%者評價為合格。 [數2] 長光程之透明彳貝耗率=100-長光程之光透射率-(反射率χ2) (9)耐光性 籲 使用IKG公司製造之單抽擠出機PMS40,於料缸溫度為 230Ό之條件下,以99 : 〇·5 : 0.5之質量比熔融混練三菱麗 陽(股)公司製造之ΡΜΜΑ VH5、汽巴精化(股)公司製造之 紫外線吸收劑Tinuvin Ρ、及Clariant Japan(股)公司製^之 光穩定劑Hostavin PR-25,而獲得紫外光濾光片用樹脂。 利用電動射出成形機(股)日本製鋼所公司製造之;350£1^111 於270°C之成形溫度下將該樹脂成形,而獲得縱向為292·5 mm、橫向為220 mm、厚度為2 mm之紫外光滤光片。關於 145347.doc -23- 201030027 該紫外光濾光片,已確認到波長未達400 nm之光幾乎不透 射。 將實施例·比較例中獲得之苯乙烯系樹脂之成形體與紫 外光濾光片重疊,使用atlas公司製造之耐候計Ci65A, 於溫度為63。(:、照射強度為0.35 W/m2(340 nm下之強度)之 條件下,自备、外光;慮光片側照射氤氣光源之光2 〇 〇小時。 亦即,使透射紫外光濾光片之400 nm以上之光照射苯乙稀 系樹脂之成形體。使用曰本電色工業(股)公司製造之色差 計Σ80,依據JIS K7105測定經光照射之成形體之2爪爪部之 b值(單位二),並根據下式計算出处。將^未達丨者評價 為合格。 △ b=照射200小時後之b值一照射前之b值 145347.doc 24· 201030027 比較例3 1 1苯乙烯-5 | | &lt;0.1 1 CN 0.17 1 cn Ο 83.7 1.54652 I \〇 l&gt; CN 比較例2 |苯乙烯-3J 寸 1-H 〇 CN 0.17 _ 1 CO ο 82.5 1.54652 VO — cn 00 寸 Ο Ltb較例1 1 丨 &lt;0.1 ο 〇 Ο 丨 1.77— 1 CN Ο 87.9 1.494 a\ rn rn — ο 實施例6 |苯乙烯-4 I &lt;0.1 CN L0J7 I (S ο 84.7 1.54652 VO ο |實施例5 ! |苯乙烯-2 I 卜 Ο (N 〇·ΐ7 1 CN Ο 83.6 1.54652 'Ο (N (Ν Ο 實施例4 | 苯乙烯-1 丨&lt;〇] Ο T*H 〇 r-H 〇 0.09 (N Ο m oo 1.595 ιτί in v〇 Ο 實施例3 苯乙烯-11 1 &lt;〇.ι 1 Ο i-H 1—H ON 00 0.58 (N Ο 87.7 1.50511 — (N 寸 ο 實施例2 苯乙烯-1 1 &lt;〇] 1 ο o 寸 § 0.21 CN Ο 1.5344 — — ο 實施例1 苯乙烯-1 1 &lt;〇.ι 1 Ο (N 〇·17 1 CN Ο 86.4 1.54652 — ο a α &amp; ε α ο. Wt% Wt% 1 1 I 苯乙烯之種類 聚合抑制劑 苯基乙快系化合物 苯乙烯 MMA 吸濕性 透明性(Haze) 長光程之透明性(光透射率) 折射率 反射率 長光程之透明損耗 耐光性(Ab) -25- 145347.doc 201030027 觀察表1得知’本發明之實施例之光學用成形體係吸濕 性較低,於長光程中之光透射率之損耗較少且耐光性良 好。 [比較例1] 將苯乙烯-1設為0質量分、MMA-1設為100質量份,除此 以外’以與實施例!相同之方式進行。將其結果示於表卜 [比較例2] 使用苯乙烯-3來代替苯乙埽],除此以外,以與實施例 1相同之方式進行。將其結果示於表 [比較例3] ® 使用苯乙烯-5來代替苯乙烯,除此以外,以與實施例 1相同之方式進行。將其結果示於表1。 &lt;考察&gt; 本發明之實施例之光學用成形體由於吸濕性較低故魅曲 或尺寸變化較少,於長光程中之光透射率之損耗較少,且 400 nm以上之耐光性良好。 於比較例1中,因僅使用丙烯酸系樹脂,故吸濕性明顯 ❿ 較高。 又,於比較例2中,長光程之光透射率較低,長光程之 光透射率損耗較大◦進而,得知Δ1)之值較大而耐光性差。 可認為其原因在於聚合抑制劑之含量為1〇 ppm以上。 又’於比較例3中,得知長光程之透明損耗較大,尤其 是Ab之值明顯較大而耐光性不良。可認為其原因在於苯基 乙炔系化合物之含量為5〇{){)111以上。 145347.doc -26- 201030027 如上所述’本發明之光學用成形體由於吸濕性較低故魅 曲或尺寸變化較少,於長光程中之光透射率較高,且财光 性良好。 又,於使用本發明之光學用成形體作為導光板之情形 '時,作為液晶顯示器用之導光板或照明用之導光板較為有 -用’尤其’因對於400 nm以上之波長的光之耐光性良好, 故作為以LED為光源之中〜大型液晶顯示器用之導光板較 為有用。 ® [光擴散體] 使用實施例就本發明之光擴散體之詳細内容加以說明, 但本發明並不限定於下述實施例。 [苯乙烯系樹脂] 就實施例及比較例中使用之苯乙烯系樹脂加以說明。 將藉由實施例1之方法獲得之苯乙烯系樹脂稱作苯乙稀 系樹脂1。將藉由實施例2之方法獲得之苯乙烯系樹脂稱作 φ 苯乙烯系樹脂2。將藉由實施例3之方法獲得之苯乙烯系樹 脂稱作苯乙烯系樹脂3。將藉由實施例4之方法獲得之苯乙 烯系樹脂稱作苯乙烯系樹脂4。 將使用苯乙稀2並藉由與實施例1相同之方法獲得之苯乙 烯系樹脂稱作苯乙烯系樹脂5。將使用苯乙烯2並藉由與實 施例2相同之方法獲得之苯乙烯系樹脂稱作苯乙烯系樹脂 6。將使用苯乙烯2並藉由與實施例3相同之方法獲得之苯 乙烯系樹脂稱作苯乙烯系樹脂7。將使用苯乙烯2並藉由與 實施例4相同之方法獲得之苯乙烯系樹脂稱作苯乙烯系樹 145347.doc •27· 201030027 脂8。 將使用苯乙烯3並藉由與實施例〗相同之方法獲得之苯乙 缚系樹脂稱作苯乙稀系樹脂9。將使用苯乙稀3並藉由與實 施例2相同之方法獲得之苯乙稀系樹脂稱作苯乙稀系樹脂 10。將使用苯乙烯3並藉由與實施例3相同之方法獲得之苯 乙烯系樹脂稱作苯乙烯系樹脂”。將使用苯乙烯3並藉由 與實施例4相同之方法獲得之苯乙稀系樹脂稱作苯乙稀系 樹脂12。 將使用苯乙烯4並藉由與實施例!相同之方法獲得之苯乙 烯系樹脂稱作苯乙烯系樹脂13。將使用苯乙烯4並藉由與 實施例2相同之方法獲得之苯乙稀系樹脂稱作苯乙稀系樹 月曰14。將使用苯乙烯4並藉由與實施例3相同之方法獲得之 苯乙浠系樹脂稱作苯乙烯系樹脂15。將使用苯乙烯4並藉 由與實施例4相同之方法獲得^乙稀系樹脂稱作苯乙烯 系樹脂16。 將使用笨乙烯5並藉由與實施例丨相同之方法獲得之苯乙 烯系樹脂稱作苯乙烯系樹脂17。將使用苯乙烯5並藉由與 實施例2相同之方法獲得之苯乙烯系樹脂稱作苯乙烯系樹 脂18。將使用苯乙烯5並藉由與實施例3相同之方法獲得之 苯乙烯系樹脂稱作苯乙烯系樹脂19。將使用苯乙烯5並藉 由與實施例4相同之方法獲得之苯乙烯系樹脂稱作苯乙烯 系樹脂20。 [實施例7] 使用東芝機械(股)製造之雙軸擠出機Τεμ·35Β,於前端 145347.doc -28- 201030027 溫度為230°C之條件下,混練混合苯乙烯系樹脂1與作為光 擴散劑之根本特殊化學(股)製造之碳酸鈣(製品名:(8) Transparent loss rate of long pathlength The transparent loss rate (unit: %) was calculated by the following formula using the light transmittance of the long path length measured in (5) and the reflectance calculated in (7). Furthermore, multiplying the reflectance by two times indicates both the light incident surface and the light exit surface. Those who did not reach 8% were evaluated as qualified. [Number 2] Transparent optical mussel rate for long path length = 100 - long light path light transmittance - (reflectance χ 2) (9) Light resistance is called the use of single-extrusion extruder PMS40 manufactured by IKG, at the cylinder temperature Under the conditions of 230 ,, the 紫外线 H VH5 manufactured by Mitsubishi Rayon Co., Ltd., and the UV absorber Tinuvin 制造 manufactured by Ciba Specialty Chemicals Co., Ltd., and Clariant Japan (by mass ratio of 99: 〇·5: 0.5) The company's light stabilizer, Hostavin PR-25, is used to obtain a resin for UV filters. It was manufactured by Nippon Steel Works Co., Ltd. using an electric injection molding machine. The resin was molded at a forming temperature of 270 ° C to obtain a longitudinal direction of 292·5 mm, a lateral direction of 220 mm, and a thickness of 2 Mm UV filter. About 145347.doc -23- 201030027 This UV filter has confirmed that light with a wavelength of less than 400 nm is almost opaque. The molded article of the styrene resin obtained in the examples and the comparative examples was superposed on the ultraviolet light filter, and a weather meter Ci65A manufactured by Atlas Co., Ltd. was used at a temperature of 63. (:, under the condition of an irradiation intensity of 0.35 W/m2 (intensity at 340 nm), self-prepared and external light; the side of the light-receiving sheet is irradiated with light of the xenon source for 2 。 hours. That is, the transmission ultraviolet light is filtered. The light of 400 nm or more of the sheet is irradiated with a molded body of a styrene-based resin, and the color difference meter Σ80 manufactured by Sakamoto Electric Co., Ltd. is used, and the claws of the 2 claw portions of the light-irradiated molded body are measured in accordance with JIS K7105. Value (unit 2), and calculate the source according to the following formula. The person who has not reached the 评价 is evaluated as qualified. △ b = b value after 200 hours of irradiation b value before irradiation 145347.doc 24· 201030027 Comparative Example 3 1 1 Styrene-5 | | &lt;0.1 1 CN 0.17 1 cn Ο 83.7 1.54652 I \〇l&gt; CN Comparative Example 2 | Styrene-3J inch 1-H 〇CN 0.17 _ 1 CO ο 82.5 1.54652 VO — cn 00 inch Ο Ltb is compared with Example 1 1 丨 &lt;0.1 ο 〇Ο 丨1.77 - 1 CN Ο 87.9 1.494 a rn rn - ο Example 6 | Styrene-4 I &lt;0.1 CN L0J7 I (S ο 84.7 1.54652 VO ο | Example 5 ! | Styrene-2 I Ο (N 〇·ΐ7 1 CN Ο 83.6 1.54652 'Ο (N (Ν 实施 Example 4 | Styrene-1 丨&lt;〇] Ο T*H 〇rH 〇0.09 (N Ο m oo 1.595 ιτί in v〇Ο Example 3 Styrene-11 1 &lt; 〇.ι 1 Ο iH 1—H ON 00 0.58 (N Ο 87.7 1.50511 — (N inch ο Example 2 styrene -1 1 &lt;〇] 1 ο o inch § 0.21 CN Ο 1.5344 — — ο Example 1 Styrene-1 1 &lt;〇.ι 1 Ο (N 〇·17 1 CN Ο 86.4 1.54652 — ο a α & ε α ο. Wt% Wt% 1 1 I Type of styrene Polymerization inhibitor Phenylethyl fast compound styrene MMA Hygroscopic transparency (Haze) Long pathlength transparency (light transmittance) Refractive index reflectance Transparent light loss and light fastness of long optical path (Ab) -25-145347.doc 201030027 It is observed that the optical forming system of the embodiment of the present invention has low hygroscopicity and a loss of light transmittance in a long optical path. Less and good light resistance. [Comparative Example 1] The styrene-1 was set to 0 mass%, and the MMA-1 was set to 100 parts by mass. The same way. The results are shown in the same manner as in Example 1 except that styrene-3 was used instead of phenelzine. The results are shown in the table. [Comparative Example 3] The same procedure as in Example 1 was carried out except that styrene-5 was used instead of styrene. The results are shown in Table 1. <Inspection> The optical molded article according to the embodiment of the present invention has less hygroscopicity or less dimensional change, less loss of light transmittance in a long optical path, and good light resistance of 400 nm or more. . In Comparative Example 1, since only the acrylic resin was used, the hygroscopicity was significantly higher. Further, in Comparative Example 2, the light transmittance of the long optical path was low, and the light transmittance loss of the long optical path was large. Further, it was found that the value of Δ1) was large and the light resistance was poor. The reason for this is considered to be that the content of the polymerization inhibitor is 1 〇 ppm or more. Further, in Comparative Example 3, it was found that the transparency loss of the long path length was large, and in particular, the value of Ab was significantly large and the light resistance was poor. This is considered to be because the content of the phenylacetylene compound is 5 〇{){) 111 or more. 145347.doc -26-201030027 As described above, the molded article for optics of the present invention has less fascination or dimensional change due to lower hygroscopicity, higher light transmittance in a long optical path, and good gravitational properties. Further, when the optical molded article of the present invention is used as the light guide plate, it is used as a light guide plate for a liquid crystal display or a light guide plate for illumination, and is particularly resistant to light of a wavelength of 400 nm or more. Since it is good in performance, it is useful as a light guide plate for a large liquid crystal display. ® [Light diffuser] The details of the light diffuser of the present invention will be described using the examples, but the present invention is not limited to the following examples. [Styrene-Based Resin] The styrene-based resins used in the examples and comparative examples will be described. The styrene resin obtained by the method of Example 1 is referred to as styrene resin 1. The styrene resin obtained by the method of Example 2 is referred to as φ styrene resin 2. The styrene resin obtained by the method of Example 3 is referred to as a styrene resin 3. The styrene-based resin obtained by the method of Example 4 is referred to as styrene-based resin 4. The styrene-based resin obtained by the same method as that of Example 1 using styrene 2 is referred to as a styrene-based resin 5. The styrene resin obtained by the same method as in Example 2 using styrene 2 is referred to as a styrene resin 6. A styrene-based resin obtained by the same method as that of Example 3 using styrene 2 is referred to as a styrene-based resin 7. The styrene resin which was obtained by using the styrene 2 and obtained by the same method as in Example 4 was called styrene tree 145347.doc • 27· 201030027 Grease 8. A styrene-based resin which is obtained by using the same method as in the example of the styrene 3 is referred to as a styrene-based resin 9. The styrene resin obtained by the same method as in Example 2 using styrene 3 is referred to as a styrene resin 10. A styrene-based resin obtained by the same method as that of Example 3 using styrene 3 is referred to as a styrene-based resin. A styrene-based resin obtained by the same method as in Example 4 using styrene 3 will be used. The resin is referred to as styrene-based resin 12. The styrene-based resin obtained by the same method as in Example! using styrene 4 is referred to as styrene-based resin 13. Styrene 4 will be used and by way of Examples 2 The styrene resin obtained by the same method is called styrene tree ruthenium 14. The styrene resin which is obtained by the same method as in Example 3 using styrene 4 is called styrene resin. 15. Styrene 4 was used and obtained by the same method as in Example 4, which was called a styrene resin 16. Styrene 5 was used and styrene obtained by the same method as in Example 将 was used. The resin is referred to as a styrene resin 17. The styrene resin obtained by the same method as that of Example 2 using styrene 5 is referred to as a styrene resin 18. Styrene 5 will be used and by way of Examples 3 styrene resin obtained by the same method The styrene resin was used. The styrene resin obtained by the same method as that of Example 4 using styrene 5 was referred to as a styrene resin 20. [Example 7] A pair manufactured using Toshiba Machine Co., Ltd. The shaft extruder Τεμ·35Β, at the front end of 145347.doc -28- 201030027 at a temperature of 230 ° C, mixing and mixing styrene resin 1 with calcium carbonate (as a special special chemical (stock) made as a light diffusing agent ( Product Name:

Lumipearl DSN-7)使其混合比達到96質量% : 4質量%,而 獲传顆粒形狀之樹脂組合物。使用日本製鋼所(股)製造之 射出成形機J140AD-180H,於料缸溫度為230°C、模具溫 度為60°C之條件下將該顆粒形狀之樹脂組合物成形,而獲 得縱向為90 mm、橫向為90 mm、厚度為2 mm之成形體。 [實施例8] 使用苯乙烯系樹脂1作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯丙烯酸系粒子(製品名:Tech_ Polymer MBX-8)作為光擴散劑,除此以外’以與實施例7 相同之方式進行。 [實施例9] . 使用98質量%之苯乙烯系樹脂!作為苯乙烯系樹脂且 使用 2質量 %iMomentive Performance Materials 製造之矽 氧烷樹脂粒子(製品名:ToSpeaH 12〇)作為光擴散劑,除此 以外’以與實施例7相同之方式進行。 [實施例10] 使用苯乙烯系樹脂2作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯苯乙烯粒子(製品名:了“匕Lumipearl DSN-7) was allowed to have a mixing ratio of 96% by mass: 4% by mass, and a resin composition having a particle shape was obtained. Using a injection molding machine J140AD-180H manufactured by Nippon Steel Works Co., Ltd., the pellet-shaped resin composition was molded under the conditions of a cylinder temperature of 230 ° C and a mold temperature of 60 ° C to obtain a longitudinal direction of 90 mm. A molded body having a lateral direction of 90 mm and a thickness of 2 mm. [Example 8] A styrene-based resin 1 was used as a styrene-based resin, and a cross-linked acrylic particle (product name: Tech_Polymer MBX-8) produced by Sekisui Chemicals Co., Ltd. was used as a light diffusing agent. Other than 'in the same manner as in Example 7. [Example 9] . 98% by mass of styrene resin was used! A methacrylic resin particle (product name: ToSpea H 12 Å) manufactured by using 2% by mass of iMomentive Performance Materials was used as a light diffusing agent, except that it was carried out in the same manner as in Example 7. [Example 10] The styrene-based resin 2 was used as the styrene-based resin, and the cross-linked styrene particles (product name: "匕" manufactured by the Sekisui Chemicals Co., Ltd. were used.

Polymer SBX_8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 [實施例11] 使用苯乙烯系樹脂2作為苯乙㈣樹脂,且使用根本特 145347.doc -29- 201030027 殊化學(股)製造之碳酸鈣(製品名:LUmipeari DSN_7)作為 光擴散劑,除此以外’以與實施例7相同之方式進行。 [實施例12] 使用98質量。/〇之苯乙烯系樹脂2作為苯乙烯系樹脂,且 使用 2 質量 % 之 Momentive Performance Materials 製造之石夕 氧烷樹脂粒子(製品名:Tospearl 120)作為光擴散劑,除此 以外’以與實施例7相同之方式進行。 [實施例13] 使用苯乙烯系樹脂3作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯苯乙烯粒子(製品名:Tech_ Polymer SBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 [實施例14] 使用苯乙烯系樹脂3作為苯乙烯系樹脂,且使用根本特 殊化學(股)製造之碳酸每(製品名:Lumipearl DSN-7)作為 光擴散劑’除此以外,以與實施例7相同之方式進行。 [實施例15] 使用苯乙烯系樹脂4作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯丙烯酸系粒子(製品名:Teeh_ Polymer MBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 [實施例16] 使用苯乙烯系樹脂5作為苯乙烯系樹脂,且使用根本特 殊化學(股)製造之碳酸舞(製品名:Lumipearl DSN-7)作為 145347.doc -30- 201030027 光擴散劑,除此以外,以與實施例7相同之方式進行。 [實施例17] 使用苯乙烯系樹脂5作為笨乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯丙烯酸系粒子(製品名:Tech_ Polymer MBX-8)作為光擴散劑,除此以外,以與實施例7 •相同之方式進行。 [實施例18] 使用98質量%之苯乙烯系樹脂5作為苯乙烯系樹脂,且 籲 使用 2 質量 〇/〇iMomentive Performance Materials 製造之石夕 氧烷樹脂粒子(製品名:T〇spearl 12〇)作為光擴散劑,除此 以外’以與實施例7相同之方式進行。 [實施例19] 使用苯乙烯系樹脂6作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯苯乙烯粒子(製品名:Tech_ Polymer SBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 w [實施例20] 使用笨乙烯系樹脂6作為苯乙烯系樹脂,且使用根本特 殊化學(知)製造之奴酸約(製品名:Lumipearl DSN-7)作為 光擴散劑’除此以外’以與實施例7相同之方式進行。 [實施例21] 使用98質量%之苯乙烯系樹脂6作為苯乙烯系樹脂,且 使用 2 質量 %iM〇mentive Performance Materials製造之妙 氧烷樹脂粒子(製品名:Tospearl 120)作為光擴散劑,除此 145347.doc -31- 201030027 以外’以與實施例7相同之方式進行。 [實施例22] 使用苯乙烯系樹脂7作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯苯乙烯粒子(製品名: Polymer SBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 [實施例2;3] 使用苯乙烯系樹脂7作為笨乙烯系樹脂,且使用根本特 殊化學(股)製造之碳_酸|弓(製品名:Lumipearl DSN-7)作為 參 光擴散劑’除此以外’以與實施例7相同之方式進行。 [實施例24] 使用苯乙烯系樹脂8作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯丙烯酸系粒子(製品名:Tech_ Polymer MBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 [實施例25] 使用苯乙烯系樹脂13作為苯乙烯系樹脂,且使用根本特 n 殊化學(股)製造之破酸約(製品名:Lumipearl DSN-7)作為 光擴散劑,除此以外,以與實施例7相同之方式進行。 [實施例26] 使用本乙烤系樹脂13作為苯乙稀系樹脂,且使用積水化 成品工業(股)製造之交聯丙烯酸系粒子(製品名:Teeh_ Polymer MBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 145347.doc -32- 201030027 [實施例27] 使用98質量%之苯乙烯系樹脂13作為苯乙烯系樹脂,且 使用 2質量 %iMomentive Performance Materials 製造之石夕 氧烷樹脂粒子(製品名:Tospearl 120)作為光擴散劑,除此 以外,以與實施例7相同之方式進行。 [實施例28] 使用苯乙烯系樹脂14作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯苯乙稀粒子(製品名:Tech-# Polymer SBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 [實施例29] 使用苯乙烯系樹脂14作為苯乙烯系樹脂,且使用根本特 殊化學(股)製造之碳酸鈣(製品名:Lumipearl DSN-7)作為 光擴散劑,除此以外,以與實施例7相同之方式進行。 [實施例30] 使用98質量%之苯乙烯系樹脂14作為苯乙烯系樹脂,且 使用 2 質量 %iMomentive Performance Materials製造之石夕 氧烷樹脂粒子(製品名:Tospearl 120)作為光擴散劑,除此 以外,以與實施例7相同之方式進行。 [實施例31] 使用苯乙烯系樹脂1 5作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯苯乙烯粒子(製品名:Tech-Polymer SBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 145347.doc •33- 201030027 [實施例32] 使用苯乙烯系樹脂15作為苯乙烯系樹脂,且使用根本特 殊化學(股)製造之碳酸鈣(製品名:Lumipeari DSN-7)作為 光擴散劑,除此以外,以與實施例7相同之方式進行。 [實施例33] 使用苯乙烯系樹脂16作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯丙烯酸系粒子(製品名:Tech_ Polymer MBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 參 [比較例4] 使用苯乙烯系樹脂9作為苯乙烯系樹脂,且使用根本特 殊化學(股)製造之碳酸鈣(製品名:Lumipearl DSN7)作為 光擴散劑,除此以外,以與實施例7相同之方式進行。 [比較例5] 使用苯乙烯系樹脂9作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯丙烯酸系粒子(製品名: P吻贿mBX_8)作為光擴散劑,除此以外,以與實施例7⑩ 相同之方式進行。 [比較例6] 使用98質量%之苯乙稀系樹脂9作為苯乙稀系樹脂,且 使用2質量kMGmentive PerfGma⑽編㈣s製造之石夕 氧燒樹脂粒子(製品名:T〇spead 12〇)作為光擴散劑,除此 以外,以與實施例7相同之方式進行。 [比較例7] 145347.doc • 34 - 201030027 使用苯乙稀系樹脂1 〇作為苯乙稀系樹脂,且使用積水化 成品工業(股)製造之交聯苯乙烯粒子(製品名:Tech_ Polymer SBX-8)作為光擴散劑’除此以外,以與實施例7 相同之方式進行。 [比較例8] 使用苯乙烯系樹脂10作為苯乙烯系樹脂,且使用根本特 殊化學(股)製造之奴酸約(製品名:Lumipearl DSN·7)作為 光擴散劑,除此以外,以與實施例7相同之方式進行。 ® [比較例9] 使用98質量%之苯乙烯系樹脂1〇作為苯乙烯系樹脂,且 使用 2 質量。/〇之 Momentive Performance Materials 製造之石夕 氧烧樹脂粒子(製品名:Tospearl 120)作為光擴散劑,除此 以外,以與實施例7相同之方式進行。 [比較例10] 使用苯乙烯系樹脂11作為苯乙稀系樹脂,且使用積水化 φ 成品工業(股)製造之交聯苯乙烯粒子(製品名:Tech-Polymer SBX_8) was carried out in the same manner as in Example 7 except that it was a light diffusing agent. [Example 11] A styrene-based resin 2 was used as a benzene (tetra) resin, and calcium carbonate (product name: LUmipeari DSN_7) manufactured by a special 145347.doc -29-201030027 special chemical company was used as a light diffusing agent. Other than this, it was carried out in the same manner as in Example 7. [Example 12] 98 mass was used. The styrene-based resin 2 is a styrene-based resin, and 2% by mass of a sulphur oxide resin particle (product name: Tospearl 120) manufactured by Momentive Performance Materials is used as a light diffusing agent, and Example 7 was carried out in the same manner. [Example 13] A styrene resin 3 was used as a styrene resin, and a crosslinked styrene particle (product name: Tech_Polymer SBX-8) manufactured by Sekisui Kogyo Co., Ltd. was used as a light diffusing agent. Except in the same manner as in Example 7, except that. [Example 14] A styrene-based resin 3 was used as a styrene-based resin, and carbonic acid (manufactured by Lumipearl DSN-7) manufactured by a fundamental special chemical (product) was used as a light diffusing agent. Example 7 was carried out in the same manner. [Example 15] The styrene-based resin 4 was used as the styrene-based resin, and the crosslinked acrylic particles (product name: Teeh_Polymer MBX-8) produced by the Sekisui Chemicals Co., Ltd. were used as the light diffusing agent. Except in the same manner as in Example 7, except that. [Example 16] A styrene-based resin 5 was used as a styrene-based resin, and a carbonated dance (product name: Lumipearl DSN-7) manufactured by a radical special chemical (product) was used as a light diffusing agent of 145347.doc -30-201030027, Except for this, it was carried out in the same manner as in Example 7. [Example 17] A styrene-based resin 5 was used as a stupid vinyl resin, and a crosslinked acrylic particle (product name: Tech_Polymer MBX-8) produced by Sekisui Chemicals Co., Ltd. was used as a light diffusing agent. Except that the same procedure as in Example 7 was carried out. [Example 18] 98% by mass of a styrene-based resin 5 was used as the styrene-based resin, and the use of a 2 mass 〇/〇i Momentive Performance Materials-based alumite resin particle (product name: T〇spearl 12〇) was used. Other than the above, 'the light diffusing agent was carried out in the same manner as in Example 7. [Example 19] A styrene-based resin 6 was used as a styrene-based resin, and a crosslinked styrene particle (product name: Tech_Polymer SBX-8) manufactured by Sekisui Chemicals Co., Ltd. was used as a light diffusing agent. Except in the same manner as in Example 7, except that. [Example 20] A stupid vinyl resin 6 was used as a styrene resin, and a saponic acid (product name: Lumipearl DSN-7) manufactured by a fundamental special chemical (product name: Lumipearl DSN-7) was used as a light diffusing agent 'other than This was carried out in the same manner as in Example 7. [Example 21] 98% by mass of a styrene-based resin 6 was used as a styrene-based resin, and aurethane resin particles (product name: Tospearl 120) manufactured by using 2% by mass of iM〇mentive Performance Materials was used as a light diffusing agent. Except this 145347.doc -31- 201030027, 'in the same manner as in Example 7. [Example 22] The styrene-based resin 7 was used as the styrene-based resin, and the crosslinked styrene particles (product name: Polymer SBX-8) manufactured by Sekisui Chemicals Co., Ltd. were used as the light diffusing agent. This was carried out in the same manner as in Example 7. [Example 2; 3] A styrene-based resin 7 was used as a stupid vinyl resin, and a carbon-acid|bow (product name: Lumipearl DSN-7) manufactured by a fundamental special chemical (product name) was used as a light diffusing agent' Other than this, it was carried out in the same manner as in Example 7. [Example 24] The styrene-based resin 8 was used as the styrene-based resin, and the crosslinked acrylic particles (product name: Tech_Polymer MBX-8) produced by Sekisui Chemicals Co., Ltd. were used as the light diffusing agent. Except in the same manner as in Example 7, except that. [Example 25] A styrene-based resin 13 was used as the styrene-based resin, and a decomposing acid (product name: Lumipearl DSN-7) manufactured by the radically special chemical (manufactured by the company) was used as a light diffusing agent, and This was carried out in the same manner as in Example 7. [Example 26] The present Baked resin 13 was used as the styrene-based resin, and the crosslinked acrylic particles (product name: Teeh_ Polymer MBX-8) produced by Sekisui Chemicals Co., Ltd. were used as the light diffusing agent. Except for this, it was carried out in the same manner as in Example 7. 145347.doc -32- 201030027 [Example 27] 98% by mass of styrene-based resin 13 was used as a styrene-based resin, and 2% by mass of iMomentive Performance Materials made of a sulphur oxide resin particle (product name: Tospearl 120) The same procedure as in Example 7 was carried out except that the light diffusing agent was used. [Example 28] A styrene-based resin 14 was used as a styrene-based resin, and crosslinked styrene particles (product name: Tech-# Polymer SBX-8) manufactured by Sekisui Chemicals Co., Ltd. were used as a light diffusing agent. Except for this, it was carried out in the same manner as in Example 7. [Example 29] A styrene-based resin 14 was used as a styrene-based resin, and calcium carbonate (product name: Lumipearl DSN-7) manufactured by a radical special chemical (product name: Lumipearl DSN-7) was used as a light diffusing agent, and Example 7 was carried out in the same manner. [Example 30] 98% by mass of the styrene-based resin 14 was used as the styrene-based resin, and the alumite resin particles (product name: Tospearl 120) manufactured by 2% by mass of iMomentive Performance Materials were used as the light diffusing agent. Except for this, it was carried out in the same manner as in Example 7. [Example 31] A styrene-based resin 15 was used as a styrene-based resin, and a crosslinked styrene particle (product name: Tech-Polymer SBX-8) manufactured by Sekisui Chemicals Co., Ltd. was used as a light diffusing agent. Except for this, it was carried out in the same manner as in Example 7. 145347.doc •33-201030027 [Example 32] A styrene-based resin 15 was used as a styrene-based resin, and calcium carbonate (product name: Lumipeari DSN-7) manufactured by a fundamental special chemical (product) was used as a light diffusing agent. Except for this, it was carried out in the same manner as in Example 7. [Example 33] The styrene-based resin 16 was used as the styrene-based resin, and the crosslinked acrylic particles (product name: Tech_Polymer MBX-8) produced by Sekisui Chemicals Co., Ltd. were used as the light diffusing agent. Except in the same manner as in Example 7, except that. [Comparative Example 4] A styrene-based resin 9 was used as the styrene-based resin, and calcium carbonate (product name: Lumipearl DSN7) manufactured by the fundamental special chemical (product name) was used as the light diffusing agent, and the examples and examples were used. 7 is done in the same way. [Comparative Example 5] The styrene-based resin 9 was used as the styrene-based resin, and the crosslinked acrylic particles (product name: P kiss bribe mBX_8) produced by the Sekisui Chemicals Co., Ltd. were used as the light diffusing agent. This was carried out in the same manner as in Example 710. [Comparative Example 6] 98% by mass of styrene-based resin 9 was used as the styrene-based resin, and as a kiln-oxygen resin particle (product name: T〇spead 12〇) manufactured by 2 mass kMGmentive PerfGma (10) (4) s, Except for the light diffusing agent, the same procedure as in Example 7 was carried out. [Comparative Example 7] 145347.doc • 34 - 201030027 The use of styrene-based resin 1 〇 as a styrene-based resin, and the use of cross-linked styrene particles manufactured by Sekisui Chemicals Co., Ltd. (product name: Tech_ Polymer SBX) -8) The same procedure as in Example 7 was carried out except that the light diffusing agent was used. [Comparative Example 8] A styrene-based resin 10 was used as a styrene-based resin, and a saponic acid (product name: Lumipearl DSN·7) manufactured by a radical special chemical (product) was used as a light diffusing agent, and Example 7 was carried out in the same manner. ® [Comparative Example 9] 98% by mass of a styrene resin was used as a styrene resin, and 2 mass was used. The same procedure as in Example 7 was carried out except that the oxidized resin particles (product name: Tospearl 120) manufactured by Momentive Performance Materials was used as a light diffusing agent. [Comparative Example 10] A styrene-based resin 11 was used as a styrene-based resin, and a cross-linked styrene particle manufactured by a product of hydration φ finished product (product) was used (product name: Tech-

Polymer SBX_8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 [比較例11 ] 使用苯乙烯系樹脂11作為苯乙烯系樹脂,且使用根本特 殊化學(股)製造之破酸參5(製品名:Lumipearl DSN-7)作為 光擴散劑’除此以外,以與實施例7相同之方式進行。 [比較例12] 使用苯乙烯系樹脂12作為苯乙烯系樹脂,且使用積水化 145347.d〇, •35- 201030027 成品工業(股)製造之交聯丙烯酸系粒子(製品名:Tech_ Polymer MBX-B)作為光擴散劑’除此以外,以與實施例7 相同之方式進行。 [比較例13] 使用本乙稀系樹脂17作為苯乙稀系樹脂,且使用根本特 殊化學(股)製造之碳酸鈣(製品名:Lumipearl DSN-7)作為 光擴散劑’除此以外,以與實施例7相同之方式進行。 [比較例14] 使用苯乙烯系樹脂17作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯丙烯酸系粒子(製品名:Tech_ Polymer MBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 [比較例15] 使用98質量%之苯乙烯系樹脂17作為苯乙烯系樹脂且 使用 2質量 %之 MGmentive Performance Materials製造之妙 氧烷樹脂粒子(製品名:T〇spearl 12〇)作為光擴散劑,除此 以外,以與實施例7相同之方式進行。 [比較例16] 使用苯乙烯系樹脂18作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯苯乙烯粒子(製品名:Tech_ Polymer SBX-8)作為光擴散劑’除此以外,以與實施例7 相同之方式進行。 [比較例17] 使用苯乙稀系樹脂18作為苯乙㈣樹脂,且使用根本特 145347.doc 201030027 殊化學(股)製造之碳酸鈣(製品名:Lumipeari DSN_7)作為 光擴散劑,除此以外’以與實施例7相同之方式進行。 [比較例18] 使用9 8質量%之本乙稀系樹脂18作為笨乙稀系樹脂,且 使用 2質量 %iMomentive Performance Materials製造之石夕 氧烷樹脂粒子(製品名:Tospearl 120)作為光擴散劑,除此 以外,以與實施例7相同之方式進行。 [比較例19] • 使用苯乙婦系樹脂19作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯苯乙烯粒子(製品名:Tech_ Polymer SBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 [比較例20] 使用苯乙烯系樹脂19作為苯乙烯系樹脂,且使用根本特 殊化學(股)製造之碳酸約(製品名:Lumipeari DSN-7)作為 光擴散劑,除此以外,以與實施例7相同之方式進行。 • [比較例21 ] 使用苯乙烯系樹脂2〇作為苯乙烯系樹脂,且使用積水化 成品工業(股)製造之交聯丙烯酸系粒子(製品名:Tech-Polymer MBX-8)作為光擴散劑,除此以外,以與實施例7 相同之方式進行。 對實施例7至實施例33及比較例4至比較例21之各成形體 進行以下評價。 (10)全光線透射率、Haze 根據JIS K71〇5 ’使用測霧計(日本電色工業公司製造之 145347.doc -37· 201030027 NDH5000)測定成形體之全光線透射率及Haze(單位:%)。 (11)擴散率 使用變角光度計(曰本電色工業公司製造之GC5000L)測 定成形體之各角度下之光透射率。使用特定角度下之光透 射率之數值,計算出由下式所定義之擴散率(%)(擴散率: JIS Z8113 編號 04100)。 [數3] (擴散率》 (20°光透射率&gt; ^ (70°光透射率)1 (5°光透射率)~jxl〇〇Polymer SBX_8) was carried out in the same manner as in Example 7 except that it was a light diffusing agent. [Comparative Example 11] The styrene-based resin 11 was used as the styrene-based resin, and the acid-destroying ginseng 5 (product name: Lumipearl DSN-7) manufactured by the fundamental special chemical (manufactured by the company) was used as the light diffusing agent. This was carried out in the same manner as in Example 7. [Comparative Example 12] The styrene-based resin 12 was used as the styrene-based resin, and the cross-linked acrylic particles (product name: Tech_ Polymer MBX-) manufactured by the finished product (stock) were used as hydrated 145347.d〇, 35-201030027. B) was carried out in the same manner as in Example 7 except that the light diffusing agent was used. [Comparative Example 13] The present ethylene-based resin 17 was used as a styrene-based resin, and calcium carbonate (product name: Lumipearl DSN-7) manufactured by a radical special chemical (product name: Lumipearl DSN-7) was used as a light diffusing agent. This was carried out in the same manner as in Example 7. [Comparative Example 14] The styrene-based resin 17 was used as the styrene-based resin, and the crosslinked acrylic particles (product name: Tech_Polymer MBX-8) produced by Sekisui Chemicals Co., Ltd. were used as the light diffusing agent. Except in the same manner as in Example 7, except that. [Comparative Example 15] 98% by mass of the styrene resin 17 was used as the styrene resin, and 2% by mass of the oxymethylene resin particles (product name: T〇spearl 12〇) manufactured by MGmentive Performance Materials was used as the light diffusing agent. Except for this, it was carried out in the same manner as in Example 7. [Comparative Example 16] The styrene-based resin 18 was used as the styrene-based resin, and the cross-linked styrene particles (product name: Tech_Polymer SBX-8) manufactured by Sekisui Chemicals Co., Ltd. was used as the light diffusing agent. Except in the same manner as in Example 7, except that. [Comparative Example 17] A styrene-based resin 18 was used as the benzene (tetra) resin, and calcium carbonate (product name: Lumipeari DSN_7) manufactured by the special 145347.doc 201030027 special chemical company was used as the light diffusing agent. 'In the same manner as in Example 7. [Comparative Example 18] 98% by mass of the present ethylenic resin 18 was used as the stupor-based resin, and 2% by mass of iMomentive Performance Materials manufactured by using a sulphuric acid resin particle (product name: Tospearl 120) was used as the light diffusion. The same procedure as in Example 7 was carried out except for the above. [Comparative Example 19] The use of styrene-based resin 19 as a styrene-based resin and the use of cross-linked styrene particles (product name: Tech_Polymer SBX-8) manufactured by Sekisui Chemicals Co., Ltd. as a light diffusing agent, Except for this, it was carried out in the same manner as in Example 7. [Comparative Example 20] A styrene-based resin 19 was used as a styrene-based resin, and carbonic acid (product name: Lumipeari DSN-7) manufactured by a fundamental special chemical (product name) was used as a light diffusing agent, and Example 7 was carried out in the same manner. [Comparative Example 21] A styrene resin was used as the styrene resin, and a crosslinked acrylic particle (product name: Tech-Polymer MBX-8) manufactured by Sekisui Chemicals Co., Ltd. was used as a light diffusing agent. Except for this, it was carried out in the same manner as in Example 7. Each of the molded articles of Examples 7 to 33 and Comparative Examples 4 to 21 was subjected to the following evaluation. (10) Total light transmittance, Haze The total light transmittance and Haze (unit: %) of the molded body were measured according to JIS K71〇5 ' using a fog meter (145347.doc -37·201030027 NDH5000, manufactured by Nippon Denshoku Industries Co., Ltd.). ). (11) Diffusion rate The light transmittance at each angle of the molded body was measured using a variable angle photometer (GC5000L manufactured by Sakamoto Denshoku Industries Co., Ltd.). Using the value of the light transmittance at a specific angle, the diffusivity (%) defined by the following formula (diffusion rate: JIS Z8113 No. 04100) is calculated. [Number 3] (Diffusion rate) (20° light transmittance> ^ (70° light transmittance) 1 (5° light transmittance)~jxl〇〇

cos20° cos70e j/ [ cos5。 J (12) 照度之分散 使用照度計(TOKYO OPTICAL製造之IM-3),根據JIS C7612藉由以下所示之方法測定照度。於距安裝於照明物 之成形體的垂直距離為1 m之水平面中之照度分布中,將 半值寬(單位:cm)作為照度之分散。 [照度測定方法] 取下LED照明(東芝照明技術(Toshiba Lighting &amp; Technology)製造之小型反射罩型,LEL-SL5N-F 40 W)所 附帶之罩殼,並貼附各成形體(LED晶片與成形體之距離為 8 mm)。將其於暗處點亮,放置30分鐘以上而使光源穩定 之後,測定特定場所之照度。 (13) 耐光性 於試驗品中使用實施例7至實施例33及比較例4至比較例 21之各成形體,除此以外,以與「(9)耐光性」試驗相同之 方式進行。 將上述實施例及比較例之結果示於表2至表6。 145347.doc -38- 201030027Cos20° cos70e j/ [ cos5. J (12) Dispersion of illuminance The illuminance was measured by the method shown below in accordance with JIS C7612 using an illuminometer (IM-3 manufactured by TOKYO OPTICAL). The half value width (unit: cm) is used as the dispersion of the illuminance in the illuminance distribution in the horizontal plane of the vertical distance of 1 m from the molded body mounted on the illuminating object. [Measurement method of illuminance] Remove the cover attached to the LED illumination (the small reflector type manufactured by Toshiba Lighting &amp; Technology, LEL-SL5N-F 40 W), and attach the molded body (LED chip) The distance from the shaped body is 8 mm). The light was turned on in a dark place, and after standing for 30 minutes or more to stabilize the light source, the illuminance at a specific place was measured. (13) Light resistance The molded articles of Examples 7 to 33 and Comparative Examples 4 to 21 were used in the same manner as in the "(9) Light resistance" test. The results of the above examples and comparative examples are shown in Tables 2 to 6. 145347.doc -38- 201030027

實施例15 L苯乙烯·ι I &lt;0.1 〇 ο Η ο 笨乙烯系 樹脂4 Ό ON 对 58.3 I 99.4 ' 69.5 1—^ 實施例14 笨乙烯-1 &lt;0.1 〇 as 00 苯乙烯系 樹脂3 Ό OS 寸 52.8 99.5 89.7 〇 實施例13 苯乙烯-1 &lt;0.1 〇 ON 00 笨乙烯系 樹脂3 Ό Os 寸 58.1 1 99.5 82.4 &lt;N 〇 實施例12 苯乙烯-1 &lt;0.1 〇 Ο S 苯乙烯系 樹脂2 00 On CN 59.2 , 99.3 1 78.5 〇 實施例11 笨乙烯-1 &lt;0.1 〇 ο δ 苯乙烯系 樹脂2 VD Os 寸 55.4 , 99.4 1 78.8 宕 〇 實施例10 |苯乙烯-1 1 &lt;0.1 〇 ο s 苯乙烯系 樹脂2 v〇 On 寸 68.1 99.2 58.4 宕 1-·^ 實施例9 Γ苯乙烯-1 &lt;0.1 〇 Μ 苯乙烯系 樹脂1 OO OS (N 53.6 99.5 83.4 § 〇 實施例8 苯乙烯-1 &lt;0.1 〇 CN 苯乙烯系 樹脂1 Ό ON 寸 78.3 99.0 50.0 g 〇 實施例7 苯乙烯-1 &lt;0.1 〇 苯乙烯系 樹脂1 v〇 〇\ 58.4 99.0 73.2 Ο 〇 S吟 ε α ε α wt% wt% Wt% wt% wt% Wt% Wt% cm 1 φ| 黩 φ| 蓉 鄉 ψ 4 φΗ 凝 跻 鄉 率 褒 袭 Ο 爱 Μ 令 &lt; 装 Ο 爱 &lt; 愛 璲 跻 tO Ο 1〇 Ο 骛 香 a i-4 X 奪 -39- 145347.doc 201030027 苯乙烯-2 | 卜 〇 〇 O 笨乙烯系 樹脂8 v〇 σν 寸 99.2 ' ίο rn 實施例23 苯乙烯-2 卜 〇 On OO 笨乙烯系 樹脂7 ο 寸 51.9 99.3 88.8 〇 cn (N d 實施例22 苯乙烯-2 卜 〇 00 笨乙烯系 樹脂7 对 57.6 99.1 80.6 寸 〇 實施例21 苯乙烯-2 卜 〇 〇 S 苯乙烯系 樹脂6 00 Ον (Ν 58.2 99.1 77.4 實施例20 笨乙烯-2 卜 〇 〇 § 笨乙烯系 樹脂6 ν〇 〇\ 寸 54.6 77.6 (N 〇 實施例19 苯乙烯-2 卜 〇 〇 笨乙烯系 樹脂6 Os 寸 67.5 99.2 56.8 〇 1-^ m 實施例18 苯乙烯-2 卜 〇 CN 苯乙烯系 樹脂5 00 Os CN 00 1—^ in 99.4 1—^ 實施例17 苯乙烯-2 卜 〇 &lt;N 苯乙烯系 樹脂5 Os 寸 76.8 98.8 48.1 § (N 〇 實施例16 苯乙烯-2 〇 2 &lt;N 苯乙烯系 樹脂5 Ό ΟΝ 寸 57.6 98.9 72.2 〇 (N 〇 時 B α E α wt% wt% wt% wt% wt% wt% Wt% 1 cm 1 親 d|N 鄉 *&lt;〇 Μ 屮 U »w 截 jo 離 蘅 率 率 衆 ΦΙ W t0 装 铝 &lt; 耸 Ο 案 &lt;ζ 教 璲 si 〇 硪 〇 〇 Ο 箬 香 朵 ft^· Φ4 i-4 ΐ4 4h X 奪 -40- 145347.doc 201030027Example 15 L styrene·ι I &lt;0.1 〇ο Η ο Stupid vinyl resin 4 Ό ON Pair 58.3 I 99.4 ' 69.5 1 -^ Example 14 Stupid ethylene-1 &lt;0.1 〇as 00 Styrene resin 3 Ό OS inch 52.8 99.5 89.7 〇 Example 13 Styrene-1 &lt;0.1 〇ON 00 Stupid vinyl resin 3 Ό Os inch 58.1 1 99.5 82.4 &lt;N 〇Example 12 Styrene-1 &lt;0.1 〇Ο S benzene Vinyl resin 200 00 On CN 59.2 , 99.3 1 78.5 〇 Example 11 Stupid ethylene-1 &lt;0.1 〇ο δ Styrene resin 2 VD Os inch 55.4, 99.4 1 78.8 宕〇 Example 10 | Styrene-1 1 &lt;0.1 〇ο s Styrene resin 2 v〇On inch 68.1 99.2 58.4 宕1-·^ Example 9 Indole styrene-1 &lt;0.1 苯乙烯 Styrene resin 1 OO OS (N 53.6 99.5 83.4 § 〇 Example 8 Styrene-1 &lt;0.1 〇CN Styrene Resin 1 Ό ON 78.3 99.0 50.0 g 〇 Example 7 Styrene-1 &lt;0.1 〇styrene resin 1 v〇〇\ 58.4 99.0 73.2 Ο 〇 S吟ε α ε α wt% wt% Wt% wt% wt% Wt% Wt% cm 1 φ| 黩Rongxiang ψ 4 φΗ 跻 跻 跻 跻 Ο Ο Ο Ο Ο 令 令 Ο Ο Ο Ο Ο Ο Ο Ο Ο Ο O O O O O O O i i i i i i i i i i i i 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 39 〇〇 〇〇 O Stupid vinyl resin 8 v 〇 σν 寸 99.2 ' ίο rn Example 23 Styrene-2 〇 〇 On OO Stupid vinyl resin 7 ο 寸 51.9 99.3 88.8 〇cn (N d Example 22 styrene - 2 〇 00 00 stupid vinyl resin 7 to 57.6 99.1 80.6 inch 〇 Example 21 styrene-2 〇〇 〇〇 S styrene resin 6 00 Ο ν (Ν 58.2 99.1 77.4 Example 20 stupid vinyl-2 〇〇 § stupid Vinyl resin 6 ν 〇〇 54.6 77.6 (N 〇 Example 19 styrene-2 〇〇 〇〇 stupid vinyl resin 6 Os inch 67.5 99.2 56.8 〇 1-^ m Example 18 styrene-2 〇 〇 CN benzene Vinyl resin 5 00 Os CN 00 1—^ in 99.4 1—^ Example 17 Styrene-2 Buddy &lt;N styrene resin 5 Os Inch 76.8 98 .8 48.1 § (N 〇Example 16 Styrene-2 〇2 &lt; N styrene resin 5 Ό 寸 57.6 98.9 72.2 〇 (N 〇 B α E α wt% wt% wt% wt% wt% wt % Wt% 1 cm 1 pro d|N 乡*&lt;〇Μ 屮U »w intercepting 蘅 rate rate ΦΙ W t0 loading aluminum &lt; Ο Ο case&lt;ζ 璲si 〇硪〇〇Ο musk朵^· Φ4 i-4 ΐ4 4h X 夺-40- 145347.doc 201030027

·&lt; 實施例33 1 笨乙烯-4 I &lt;0.1 3 ο r·^ ο 笨乙烯系 樹脂16 Os 寸 V〇 V-) 66.2 寸 〇 實施例32 笨乙烯-4 &lt;0.1 Os 〇〇 苯乙烯系 樹脂15 Ό ON 寸 50.9 99.3 | 87.6 ΓΠ 實施例31 苯乙烯-4 &lt;0.1 ο 00 笨乙烯系 樹脂15 Ό Os 寸 56.8 98.9 | 80.4 寸 〇 實施例30 苯乙烯-4 &lt;0.1 ο s 苯乙烯系 樹脂14 00 Os 00 VI 〇\ 〇 1- I 76.2 ί—Η CO 實施例29 苯乙烯-4 &lt;0.1 ο δ 苯乙烯系 樹脂14 VO Os 寸 OS 〇\ 宕 1-^ rn 實施例28 笨乙烯-4 &lt;0.1 ο s 苯乙烯系 樹脂14 Ό a\ 寸 66,4 99.2 1 56.6 〇 »—Η 寸 〇 實施例27 苯乙烯-4 &lt;0.1 CN 笨乙烯系 樹脂13 00 OS 50.8 99.2 1 1 81.5 〇 實施例26 苯乙烯-4 &lt;0.1 (Ν Μ 苯乙烯系 樹脂13 v〇 Os 寸 75.6 98.8 1 47.8 § rn 實施例25 苯乙烯-4 &lt;0.1 CN &lt;η Μ 笨乙烯系 樹脂13 VO ON 寸 56.8 98.9 70.3 〇 cn 〇 單位 Β g B &amp; wt% wt% ; wt% wt% wt% wt% wt% cm 1 m|N 騷 者 ΐφή 屮 ΦΙ 戥 jd # 鄉 w 率 w !〇 爱 Φ &lt; 爱 耸 tO 敦 &lt; 爱 i4 驽 齋 ¥ tO 2 Ο Ο 香 棻 a 2 ϊ4 Φ4 Μ X 樂 -41 - 145347.doc 201030027 in 比較例12 苯乙烯-3 寸 〇 〇 »—&lt; ο 苯乙烯系 樹脂12 Os 寸 55.3 65.6 1—^ rn 〇 比較例11 苯乙烯-3 寸 〇 Os 00 笨乙烯系 樹脂11 Ό On 寸 50.5 99.1 86.5 ι (N 〇 比較例10 1苯乙烯-3 寸 〇 Η OS OO 笨乙烯系 樹脂11 Ό Os 寸 αί 〇\ __Ί21__! 〇 比較例9 1苯乙烯-3 寸 〇 〇 S 笨乙烯系 樹脂10 00 ON CS 57.6 as 〇\ 76.5 〇 »—Η CN 〇 比較例8 苯乙烯-3 寸 〇 〇 笨乙烯系 樹脂10 v〇 On 寸 53.6 98.9 75.5 比較例7 苯乙烯-3 寸 〇 〇 笨乙烯系 樹脂10 ON 寸 65.7 as Os 〇 CN 〇 i比較例6 「苯乙烯-3 寸 〇 (Ν 苯乙烯系 樹脂9 00 On Os σ\ 80.6 ΓΛ 比較例5 苯乙烯-3 寸 〇 苯乙烯系 樹脂9 v〇 ON 寸 98.7 46.6 ι g 〇 比較例4 苯乙烯-3 寸 〇 (Ν 笨乙烯系 樹脂9 Os 寸 in 98.9 ο ο 1—^ 寸 〇 單位 ε α ε α wt% wt% Wt% wt% wt% wt% Wt% cm 1 Φ4 *Kr\ ♦1 龚 ΐΐί.Ι ®N ♦ # φ| m 鄉 蘅 率 爱 «Ν W Ο Μ Φ &lt; 裝 tO 装 教 璲 ±i 0 :伞 tO s Ο Ο 骛 香 Ν ϊ-4 s Φ4 Η 4h X 奪 •42- 145347.doc 201030027 比較例21 , 苯乙烯-5 | &lt;0.1 ο ο 苯乙烯系 樹脂20 v〇 ON 寸 55.3 98.8 65.7 〇 r·^ Ο) 〇 比較例20 苯乙烯-5 &lt;0.1 ί ΟΝ 00 苯乙烯系 樹脂19 v〇 On 寸 50.1 99.2 I 86.4 »Τ) 〇 比較例19 苯乙烯-5 &lt;0.1 ΟΝ 00 苯乙烯系 樹脂19 Ό ON 寸 55.8 98.9 79.6 ν〇 Ο 比較例18 苯乙烯-5 &lt;0.1 Ο δ 苯乙烯系 樹脂18 00 ON ΓΊ 56.2 98.9 〇 寸 Ο 比較例17 苯乙烯-5 &lt;0.1 1 〇 ΓΟ ί-Η ο S 苯乙烯系 樹脂18 Ό Os 寸 53.2 1 ' 98.9 75.5 〇 寸 ο 比較例16 苯乙烯-5 &lt;0.1 沄 ο 苯乙烯系 樹脂18 寸 65.7 55.5 〇 00 ο 比較例15 Π笨乙烯-5Π &lt;0.1 (Ν 笨乙烯系 樹脂17 00 Os (Ν 49.5 98,9 1 79.5 〇 ο 比較例14 苯乙烯-5 1 &lt;0.1 CN in 苯乙烯系 樹脂17 v〇 Os 寸 74.6 98.7 1 46.8 ο 比較例13 苯乙烯-5 &lt;0.1 130 &lt;Ν «Π 苯乙烯系 樹脂17 VO 55.4 98.9 1 69.8 〇 ο ε &amp; ε α Wt% wt% Wt% wt% wt% wt% wt% cm 1 黩 蓉 ♦1 屮 屮 # 騄 λ3 鄉 m 装 φ| Μ w 漆 Ο 装 4 &lt;1 爱 Ο 爱 爱 V? 齋 ±1 Ο Ο Ο Ο 骛 香 a ttsj ί-4 i4 Φ4 X m -43- 145347.doc 201030027 &lt;考察&gt; 如表2至表4所示,本發明之實施例之光學用成形體係全 光線透射率或擴散率良好,且4〇〇 nm以上之财光性良好。 可認為比較例中擴散率下降之原因在於:抑制劑之量為 10 ppm以上’或者苯基乙炔系化合物之量為5〇 ppm以上。 可認為比較例中表示耐光性之Μ值較大之原因在於:聚合 抑制劑之量為10 ppm以上,以及苯基乙炔系化合物之含量 為50 ppm以上。 如上所述,本發明之光擴散體係全光線透射率或擴散率 良好,且耐光性良好。因此,作為照明等各種用途中使用 之光擴散體較為有用。 又,由於對400 nm以上之波長的光之耐光性良好故作 為以LED為光源之光擴散體(擴散板或擴散罩等)亦較為有 用0 145347.doc • 44-&lt; Example 33 1 Stupid ethylene-4 I &lt;0.1 3 ο r·^ ο Stupid vinyl resin 16 Os inch V〇V-) 66.2 inch 〇 Example 32 Stupid ethylene-4 &lt;0.1 Os Benzene Vinyl resin 15 Ό ON inch 50.9 99.3 | 87.6 实施 Example 31 Styrene-4 &lt;0.1 ο 00 Stupid vinyl resin 15 Ό Os inch 56.8 98.9 | 80.4 inch 〇 Example 30 Styrene-4 &lt;0.1 ο s Styrene resin 14 00 Os 00 VI 〇 〇 1- I 76.2 Η Η CO Example 29 Styrene-4 &lt;0.1 ο δ Styrene resin 14 VO Os inch OS 〇\ 宕1-^ rn Example 28 Stupid ethylene-4 &lt;0.1 ο s styrene resin 14 Ό a 寸 66,4 99.2 1 56.6 〇»—Η inch 〇 Example 27 Styrene-4 &lt;0.1 CN Stupid vinyl resin 13 00 OS 50.8 99.2 1 1 81.5 〇 Example 26 Styrene-4 &lt;0.1 (Ν 苯乙烯 styrene resin 13 v 〇 Os inch 75.6 98.8 1 47.8 § rn Example 25 Styrene-4 &lt; 0.1 CN &lt;η Μ Stupid ethylene Resin 13 VO ON inch 56.8 98.9 70.3 〇cn 〇unit Β g B &amp; wt% wt% ; wt% wt% wt% wt% wt% cm 1 m|N 骚者ΐφή 屮ΦΙ 戥jd # 乡w rate w !〇爱Φ &lt; love towering tO 敦&lt; love i4 驽斋¥ tO 2 Ο Ο 棻 棻 a 2 ϊ4 Φ4 Μ X Le-41 - 145347. Doc 201030027 in Comparative Example 12 Styrene-3 inch 〇〇»—&lt; ο Styrene resin 12 Os inch 55.3 65.6 1—^ rn 〇Comparative example 11 Styrene-3 inch 〇Os 00 Stupid vinyl resin 11 Ό On Inch 50.5 99.1 86.5 ι (N 〇Comparative Example 10 1 Styrene-3 inch 〇Η OS OO Stupid vinyl resin 11 Ό Os inch αί 〇\ __Ί21__! 〇Comparative Example 9 1 Styrene-3 inch 〇〇S Stupid vinyl Resin 10 00 ON CS 57.6 as 〇\ 76.5 〇»—Η CN 〇Comparative Example 8 Styrene-3 inch 〇〇 stupid vinyl resin 10 v〇On inch 53.6 98.9 75.5 Comparative Example 7 Styrene-3 inch 〇〇 stupid ethylene Resin 10 ON inch 65.7 as Os 〇CN 〇i Comparative Example 6 "styrene - 3 inch 〇 (Ν styrene resin 9 00 On Os σ \ 80.6 ΓΛ Comparative Example 5 Styrene-3 inch styrene resin 9 v〇ON inch 98.7 46.6 ι g 〇Comparative example 4 Styrene-3 inch 〇(Ν Stupid vinyl resin 9 Os inch in 98.9 ο ο 1—^ inch 〇 unit ε α ε α wt% wt% Wt% wt% wt% wt% Wt% cm 1 Φ4 *Kr\ ♦1 Gong ΐΐ Ι N N N N N N N N N N N N N N N N N & & &&; install tO 璲 璲 ± i 0 : Umbrella tO s Ο 骛 骛 Ν ϊ 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 42 Resin 20 v〇ON inch 55.3 98.8 65.7 〇r·^ Ο) 〇Comparative Example 20 Styrene-5 &lt;0.1 ΟΝ 00 00 Styrene resin 19 v〇On inch 50.1 99.2 I 86.4 »Τ) 〇Comparative Example 19 Styrene-5 &lt;0.1 ΟΝ 00 Styrene Resin 19 Ό ON Inch 55.8 98.9 79.6 ν〇Ο Comparative Example 18 Styrene-5 &lt;0.1 Ο δ Styrene Resin 18 00 ON ΓΊ 56.2 98.9 〇Inch Ο Example 17 Styrene-5 &lt;0.1 1 〇ΓΟ ί-Η ο S Styrene resin 18 Ό Os inch 53.2 1 ' 98.9 75.5 ο ο Comparative Example 16 Styrene-5 &lt;0.1 沄ο Styrene resin 18 Inch 65.7 55.5 〇00 ο Comparative Example 15 Π Styrene-5Π &lt;0.1 (Ν Stupid vinyl resin 17 00 Os (Ν 49.5 98, 9 1 79.5 〇ο Comparative Example 14 Styrene-5 1 &lt; 0.1 CN in benzene Vinyl resin 17 v 〇 Os inch 74.6 98.7 1 46.8 ο Comparative Example 13 Styrene-5 &lt; 0.1 130 &lt; Ν «Π Styrene resin 17 VO 55.4 98.9 1 69.8 〇ο ε & ε α Wt% wt% Wt% wt% wt% wt% wt% cm 1 黩蓉♦1 屮屮# 騄λ3 Township m φ| Μ w Paint Ο Pack 4 &lt;1 Love Ο Love Love V? 斋±1 Ο Ο Ο 骛 Musk a ttsj ί-4 i4 Φ4 X m -43- 145347.doc 201030027 &lt;Exploration&gt; As shown in Tables 2 to 4, the optical forming system of the embodiment of the present invention has a good total light transmittance or diffusivity, and 4 The wealth above 〇〇 nm is good. The reason why the diffusivity is lowered in the comparative example is that the amount of the inhibitor is 10 ppm or more or the amount of the phenylacetylene compound is 5 〇 ppm or more. It is considered that the reason why the light resistance is large in the comparative example is that the amount of the polymerization inhibitor is 10 ppm or more, and the content of the phenylacetylene compound is 50 ppm or more. As described above, the light diffusing system of the present invention has a good total light transmittance or diffusivity and good light resistance. Therefore, it is useful as a light diffuser used for various applications such as illumination. Further, since light having a wavelength of 400 nm or more is excellent in light resistance, it is also useful as a light diffuser (diffusion plate or diffusion cover) using LED as a light source. 0 145347.doc • 44-

Claims (1)

201030027 七、申請專利範圍: ι_ 一種光學用成形體,其係將藉由使聚合抑制劑未達1〇 ppm 且苯基乙快系化合物為50 ppm以下之苯乙烯系單 體進行聚合反應所得之苯乙烯系樹脂成形而成者。 2·如請求項!之光學用成形體,其中上述苯乙烯系樹脂為 苯乙烯_(曱基)丙烯酸酯系共聚物。 3.如明求項1或2之光學用成形體,其中上述聚合反應為自 由基溶液聚合反應。 • 4. 一種導光板,其係使用如請求項1至3中任一項之光學用 成形體而成者。 5. —種光擴散體,其係使用如請求項丨至3中任一項之光學 用成形體而成者。 6. 如請求項5之光擴散體,其含有0.丨質量%以上、ι〇質量〇/〇 以下之選自交聯丙烯酸系粒子、交聯苯乙烯系粒子、矽 氧烧樹脂粒子及碳酸鈣之群之至少_種光擴散劑。201030027 VII. Patent application scope: ι_ An optical molded body obtained by polymerizing a styrene monomer having a polymerization inhibitor of less than 1 ppm and a phenylethyl fast compound of 50 ppm or less. A styrene resin is molded. 2. If requested! The optical molded article wherein the styrene resin is a styrene-(fluorenyl) acrylate copolymer. 3. The optical molded article according to claim 1 or 2, wherein the polymerization reaction is a free radical solution polymerization. 4. A light guide plate which is obtained by using the optical molded body according to any one of claims 1 to 3. A light-diffusing body which is obtained by using the optical molded article according to any one of claims 3 to 3. 6. The light-diffusing body of claim 5, which comprises 0. 丨 mass% or more, ι 〇 / 〇 or less selected from the group consisting of crosslinked acrylic particles, crosslinked styrene particles, bismuth oxide resin particles, and carbonic acid At least _ kinds of light diffusing agents of the group of calcium. I45347.doc 201030027 四、指定代表圖: ‘ (一) 本案指定代表圖為:(無) (二) 本代表圖之元件符號簡單說明: 五、本案若有化學式時,請揭示最能顯示發明特徵的化學式: (無) 145347.docI45347.doc 201030027 IV. Designation of representative drawings: ' (1) The representative representative of the case is: (none) (2) The symbol of the symbol of the representative figure is simple: 5. If there is a chemical formula in this case, please reveal the characteristics that can best show the invention. Chemical formula: (none) 145347.doc
TW98143189A 2008-12-17 2009-12-16 An optical molded body, a light guide plate and a light diffuser TWI471341B (en)

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