JP2007125824A - Biaxially oriented polyester film - Google Patents

Biaxially oriented polyester film Download PDF

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JP2007125824A
JP2007125824A JP2005321434A JP2005321434A JP2007125824A JP 2007125824 A JP2007125824 A JP 2007125824A JP 2005321434 A JP2005321434 A JP 2005321434A JP 2005321434 A JP2005321434 A JP 2005321434A JP 2007125824 A JP2007125824 A JP 2007125824A
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polyester
polyester film
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JP4766995B2 (en
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Toshiharu Watanabe
俊治 渡辺
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Mitsubishi Polyester Film Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a biaxially oriented polyester film which has easy adhesive properties, light scattering properties with small yellow cast of a film-transmitted light and high productivity, and can be best-suitably used, for example, with an adhesive layer or an ultraviolet-curable resin layer formed on the surface of the polyester film, and for purposes such as lamination with a glass requiring matte effect or a molded object, packaging, and as a base material film for constituent components, e.g. a prism sheet and a light scattering sheet. <P>SOLUTION: This biaxially oriented polyester film includes an easy adhesive coating layer formed at least, on one surface. In addition, the polyester film contains 0.10 to 10 wt.% organic particle having at least 300°C of 5% heat decomposition temperature and 2.0 to 40 μm average particle diameter. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本発明は、ポリエステルフィルムの表面に接着剤層や紫外線硬化樹脂層などを設けて使用される、艶消し性が必要とされるガラスや成形体貼り合わせ用途や包装用途、また液晶ディスプレイの構成部品、例えばプリズムシートや光拡散シートの基材フィルムに使用される易接着光散乱性二軸延伸ポリエステルフィルムに関する。   The present invention is used by providing an adhesive layer, an ultraviolet curable resin layer or the like on the surface of a polyester film, glass or molded product bonding or packaging applications that require matting, and liquid crystal display components. For example, the present invention relates to an easily adhesive light-scattering biaxially stretched polyester film used for a base film of a prism sheet or a light diffusion sheet.

光拡散剤を含有させた二軸延伸ポリエステルフィルムとして、特許文献1または特許文献2に、平均粒子径が数μmの無機粒子を数%含有させたポリエステルフィルムが提案されているが、樹脂押し出しラインでのフィルター圧力上昇が起こりやすく、生産性が悪いという問題がある。   As a biaxially stretched polyester film containing a light diffusing agent, Patent Document 1 or Patent Document 2 proposes a polyester film containing several percent of inorganic particles having an average particle diameter of several μm. There is a problem that the filter pressure rises easily in the case and productivity is poor.

また、特許文献3によれば、内層に架橋アクリル微粒子を含有させることによって、実質的にボイドが発生しない、全光線透過率の高い光散乱性フィルムが提案されている。しかし、有機粒子の熱分解温度が低いため、フィルムが黄色を帯びてしまう問題がある。   Patent Document 3 proposes a light-scattering film having a high total light transmittance, in which voids are not substantially generated by containing crosslinked acrylic fine particles in the inner layer. However, since the thermal decomposition temperature of the organic particles is low, there is a problem that the film becomes yellowish.

特開2002−178472号公報JP 2002-178472 A 特開2004−67853号公報JP 2004-67853 A 特開平13−272508号公報Japanese Patent Laid-Open No. 13-272508

本発明は、上記実情に鑑みなされたものであって、その解決課題は、易接着性を有し、フィルム透過光の黄色味が小さい光散乱性を有する、生産性に優れた二軸延伸ポリエステルフィルムを提供することにある。   The present invention has been made in view of the above circumstances, and the problem to be solved is a biaxially stretched polyester excellent in productivity, having easy adhesion, and having light scattering properties with small yellowness of the film transmitted light. To provide a film.

本発明者は、上記課題に鑑み鋭意検討した結果、特定の構成を有する二軸延伸ポリエステルフィルムによれば、上記課題を容易に解決できることを見いだし、本発明を完成するに至った。   As a result of intensive studies in view of the above problems, the present inventors have found that the above problems can be easily solved by a biaxially stretched polyester film having a specific configuration, and have completed the present invention.

すなわち、本発明の要旨は、少なくとも片面に易接着塗布層を有する二軸延伸ポリエステルフィルムであって、5%熱分解温度が300℃以上であり、平均粒子径が2.0〜40μmの有機粒子を0.10〜10重量%含有することを特徴とする二軸延伸ポリエステルフィルムに存する。   That is, the gist of the present invention is a biaxially stretched polyester film having an easy-adhesion coating layer on at least one side, an organic particle having a 5% thermal decomposition temperature of 300 ° C. or higher and an average particle size of 2.0 to 40 μm. Is contained in a biaxially stretched polyester film characterized by containing 0.10 to 10% by weight.

以下、本発明を詳細に説明する。
本発明におけるポリエステルとは、テレフタル酸、イソフタル酸、ナフタレン−2,6−ジカルボン酸等のような芳香族ジカルボン酸と、エチレングリコール、ジエチレングリコール、トリメチレングリコール、テトラメチレングリコール、ネオペンチルグリコール、1,4−シクロヘキサンジメタノール等のようなグリコールとのエステルを主たる成分とするポリエステルである。当該ポリエステルは、芳香族ジカルボン酸とグリコールとを直接重合させて得られるほか、芳香族ジカルボン酸ジアルキルエステルとグリコールとをエステル交換反応させた後、重縮合させる方法、あるいは芳香族ジカルボン酸のジグリコールエステルを重縮合させる等の方法によっても得られる。当該ポリエステルの代表的なものとしては、ポリエチレンテレフタレート、ポリエチレン−2,6−ナフタレンジカルボキシレート(PEN)、ボリブチレンテレフタレート等が例示される。かかるポリエステルは、共重合されないホモポリマーであってもよく、またジカルボン酸成分の40モル%以下が主成分以外のジカルボン酸成分であり、ジオール成分の40モル%以下が主成分以外のジオール成分であるような共重合ポリエステルであってもよく、またそれらの混合物であってもよい。
Hereinafter, the present invention will be described in detail.
The polyester in the present invention is an aromatic dicarboxylic acid such as terephthalic acid, isophthalic acid, naphthalene-2,6-dicarboxylic acid, ethylene glycol, diethylene glycol, trimethylene glycol, tetramethylene glycol, neopentyl glycol, 1, This polyester is mainly composed of an ester with glycol such as 4-cyclohexanedimethanol. The polyester can be obtained by directly polymerizing an aromatic dicarboxylic acid and a glycol, or by a transesterification reaction between an aromatic dicarboxylic acid dialkyl ester and a glycol, followed by polycondensation, or an aromatic dicarboxylic acid diglycol. It can also be obtained by a method such as polycondensation of an ester. Typical examples of the polyester include polyethylene terephthalate, polyethylene-2,6-naphthalenedicarboxylate (PEN), boribylene terephthalate, and the like. Such a polyester may be a homopolymer that is not copolymerized, 40 mol% or less of the dicarboxylic acid component is a dicarboxylic acid component other than the main component, and 40 mol% or less of the diol component is a diol component other than the main component. It may be a certain copolyester or a mixture thereof.

本発明では、フィルムに光散乱性を発現させるため有機粒子を含有させる。有機粒子はフィルム全体に、または2層以上の共押出し積層フィルムの少なくとも1層に含有してもよい。   In the present invention, the film contains organic particles in order to develop light scattering properties. The organic particles may be contained in the entire film or in at least one layer of a co-extruded laminated film having two or more layers.

本発明で使用する有機粒子の熱重量分析計による不活性雰囲気下の5%熱分解温度は、300℃以上である必要があり、好ましくは310℃以上である。熱分解温度が300℃未満では、熱劣化物の発生により、フィルムの透過光が黄色味を帯びて外観品質の低下が起こる。   The 5% pyrolysis temperature of the organic particles used in the present invention under an inert atmosphere by a thermogravimetric analyzer needs to be 300 ° C. or higher, preferably 310 ° C. or higher. When the thermal decomposition temperature is less than 300 ° C., the transmission light of the film becomes yellowish due to the generation of a thermally deteriorated product, resulting in a decrease in appearance quality.

本発明で用いる有機粒子の平均粒子径は2.0〜40μmの範囲であり、好ましくは2.5〜30μmの範囲である。平均粒子径が2.0μm未満では、光散乱性が低下する。一方、平均粒子径が40μmを超える場合は、フィルターの圧力上昇が大きくなり、生産性が劣る。また、用いるフィルターの目を大きくすると、フィルム中の異物が増加する。   The average particle diameter of the organic particles used in the present invention is in the range of 2.0 to 40 μm, preferably in the range of 2.5 to 30 μm. When the average particle size is less than 2.0 μm, the light scattering property is lowered. On the other hand, when the average particle diameter exceeds 40 μm, the increase in the pressure of the filter becomes large and the productivity is inferior. Moreover, if the filter eyes used are enlarged, foreign matter in the film increases.

本発明で用いる有機粒子は、表面に官能基を有することが好ましい。官能基を有する粒子は帯電しやすく粒子間の静電的な反発力が働き分散性が向上すると考えられる。官能基を有しないと粒子間で凝集しやすくなりフィルター寿命が低下する。さらにポリエステルとの親和性が低下し粒子周りに大きなボイドを形成しフィルム製造工程やフィルムの加工工程で粒子が脱落しやすくなりフィルム自身にもキズが発生しやすくなる。好ましい官能基としてはカルボン酸基、水酸基、エポキシ基、エステル基である。   The organic particles used in the present invention preferably have a functional group on the surface. It is considered that particles having a functional group are easily charged and an electrostatic repulsive force between the particles acts to improve dispersibility. Without a functional group, the particles tend to aggregate between the particles and the filter life is reduced. Furthermore, the affinity with polyester is reduced, and large voids are formed around the particles, so that the particles are easily dropped in the film manufacturing process and the film processing process, and the film itself is easily damaged. Preferred functional groups are a carboxylic acid group, a hydroxyl group, an epoxy group, and an ester group.

本発明のフィルムのフィルム全体に対する有機粒子含有量は、0.10〜10重量%の範囲であり、好ましくは0.20〜8重量%の範囲である。含有量が0.10重量%未満では、本発明が意図する光散乱性フィルムとすることができない。一方、10重量%を超えると、フィルムが破断しやすくなり、生産性が低下する。   The organic particle content of the film of the present invention is in the range of 0.10 to 10% by weight, preferably in the range of 0.20 to 8% by weight. If the content is less than 0.10% by weight, the light scattering film intended by the present invention cannot be obtained. On the other hand, if it exceeds 10% by weight, the film tends to break and productivity is lowered.

また、本発明におけるフィルム中の有機粒子は、二軸延伸の条件で変形する程度の硬さを有し、その変形度は、1.1〜5.0の範囲が好ましく、1.2〜4.0の範囲がさらに好ましい。変形度が1.1未満の有機粒子は、ポリエステル樹脂溶解温度の250〜350℃の高温下でせん断応力を受けたとき、弾性変形の程度が小さくなり、フィルターの寿命が低下すると考えられる。一方、変形度が5.0を超えると光散乱性が低下する傾向がある。   In addition, the organic particles in the film of the present invention have a hardness that can be deformed under biaxial stretching conditions, and the degree of deformation is preferably in the range of 1.1 to 5.0, and 1.2 to 4 A range of 0.0 is more preferred. The organic particles having a degree of deformation of less than 1.1 are considered to have a small degree of elastic deformation when subjected to shear stress at a polyester resin dissolution temperature of 250 to 350 ° C., and the life of the filter is reduced. On the other hand, when the degree of deformation exceeds 5.0, the light scattering property tends to decrease.

なお、本発明で使用する有機粒子は、単成分でもよく、また、2成分以上を同時に用いてもよい。具体的な有機粒子の例としては、メラミン樹脂、ポリスチレン、有機シリコーン樹脂、アクリル−スチレン共重合体等の有機粒子が挙げられる。   In addition, the organic particle used by this invention may be a single component, and may use two or more components simultaneously. Specific examples of organic particles include organic particles such as melamine resin, polystyrene, organic silicone resin, and acrylic-styrene copolymer.

また、本発明のフィルムの光沢度は、好ましくは95%以下、さらに好ましくは90%以下である。光沢度が95%以上では艶消し性が劣る傾向がある。   The gloss of the film of the present invention is preferably 95% or less, more preferably 90% or less. When the glossiness is 95% or more, the matte property tends to be inferior.

また本発明のフィルムのヘーズは、好ましくは10%以上、さらに好ましくは20%以上である。ヘーズが10%未満では光散乱性が劣ることがある。 The haze of the film of the present invention is preferably 10% or more, more preferably 20% or more. If the haze is less than 10%, the light scattering property may be inferior.

また、本発明のフィルム中には必要に応じて、紫外線吸収剤、帯電防止剤、酸化防止剤、蛍光増白剤等の添加剤を含有してもよい。   In addition, the film of the present invention may contain additives such as an ultraviolet absorber, an antistatic agent, an antioxidant, and a fluorescent brightening agent as necessary.

本発明のフィルムは、その上に存在する層との接着性を向上させるために少なくとも片面に易接着塗布層を有する必要がある。この易接着層は、通常、ポリマーおよび架橋剤を主成分として構成される。ポリマーは、例えば、水性ポリウレタン、水性ポリエステルおよび水性アクリル樹脂の少なくとも1つからなり、好ましくは、ガラス転移温度(Tg)が0℃以上、さらには40℃以上のものであり、さらに好ましくはポリウレタンの中でもポリエステルポリウレタンであり、カルボン酸残基を持ち、その少なくとも一部はアミンまたはアンモニアを用いて水性化されているものである。また架橋剤は、メラミン系、エポキシ系、オキサゾリン系樹脂が一般に用いられるが、塗布性、耐久接着性の点で、メラミン系樹脂が好ましい。   The film of the present invention needs to have an easy-adhesion coating layer on at least one side in order to improve the adhesion with the layer existing thereon. This easy-adhesion layer is usually composed mainly of a polymer and a crosslinking agent. The polymer comprises, for example, at least one of water-based polyurethane, water-based polyester, and water-based acrylic resin, and preferably has a glass transition temperature (Tg) of 0 ° C. or higher, more preferably 40 ° C. or higher, more preferably polyurethane. Among them, a polyester polyurethane has a carboxylic acid residue, and at least a part thereof is made water-based using an amine or ammonia. As the cross-linking agent, melamine-based, epoxy-based, and oxazoline-based resins are generally used, but melamine-based resins are preferable in terms of coating properties and durable adhesiveness.

塗布剤の塗布方法としては、例えば、原崎勇次著、槙書店、1979年発行、「コーティング方式」に示されるような、リバースロールコーター、グラビアコーター、ロッドコーター、エアドクターコーターまたはこれら以外の塗布装置を使用することができる。塗布層は、ポリエステルフィルムの片面だけに形成してもよいし、両面に形成してもよい。片面にのみ形成した場合、その反対面には必要に応じて上記の塗布層と異なる塗布層を形成して他の特性を付与することもできる。なお、塗布剤のフィルムへの塗布性や接着性を改良するため、塗布前にフィルムに化学処理や放電処理を施してもよい。また、表面特性をさらに改良するため、塗布層形成後に放電処理を施してもよい。   As a coating method of the coating agent, for example, a reverse roll coater, a gravure coater, a rod coater, an air doctor coater, or a coating apparatus other than these as shown in Yuji Harasaki, Tsuji Shoten, published in 1979, “Coating Method” Can be used. The coating layer may be formed only on one side of the polyester film or on both sides. When formed only on one side, other characteristics can be imparted by forming a coating layer different from the above-mentioned coating layer on the opposite surface as necessary. In addition, in order to improve the applicability | paintability and adhesiveness to the film of a coating agent, you may give a chemical process and an electrical discharge process to a film before application | coating. Further, in order to further improve the surface characteristics, a discharge treatment may be performed after the coating layer is formed.

塗布層の厚みは、最終的な乾燥厚さとして、通常0.02〜0.5μm、好ましくは0.03〜0.3μmの範囲である。塗布層の厚さが0.02μm未満の場合は、接着性が劣る。一方、塗布層の厚さが0.5μmを超える場合は、フィルムが相互に固着しやすくなる。   The thickness of the coating layer is usually in the range of 0.02 to 0.5 μm, preferably 0.03 to 0.3 μm, as the final dry thickness. When the thickness of the coating layer is less than 0.02 μm, the adhesiveness is inferior. On the other hand, when the thickness of the coating layer exceeds 0.5 μm, the films are easily fixed to each other.

さらに易滑性、離型性、帯電防止性を付与する目的のコーティング処理をフィルムの他面に行うこともできる。   Furthermore, the other surface of the film can be subjected to a coating treatment for the purpose of imparting easy slipping, releasability and antistatic properties.

本発明のフィルムの厚みは、通常20〜300μmの範囲である。フィルム厚みが20μm未満では、加工作業性が悪いことがある。一方、フィルム厚みが300μmを超えると、重量増加や取り扱い性の悪化が起こることがある。   The thickness of the film of the present invention is usually in the range of 20 to 300 μm. If the film thickness is less than 20 μm, the workability may be poor. On the other hand, when the film thickness exceeds 300 μm, an increase in weight or deterioration in handleability may occur.

次に本発明のフィルムの製造方法を具体的に説明するが、本発明の構成要件を満足する限り、以下の例示に特に限定されるものではない。   Next, although the manufacturing method of the film of this invention is demonstrated concretely, as long as the structural requirements of this invention are satisfied, it is not specifically limited to the following illustrations.

本発明のフィルムを製造するときには、乾燥したポリエステルを押出機に供給し、各ポリエステルの融点以上の温度に加熱してそれぞれ溶融させる。次いで、ポンプとフィルターを介してTダイから溶融シートとして押出す。続いて、溶融シートを回転冷却ドラム上でガラス転位温度未満にまで急冷し、非晶質の未延伸フィルムを得る。このとき、未延伸フィルムの平面性を向上させるために、静電印加密着法や液体塗布密着法等によって、未延伸フィルムと回転冷却ドラムとの密着性を向上させてもよい。そして、ロール延伸機を用いて、未延伸フィルムをその長手方向に延伸(縦延伸)することにより一軸延伸フィルムを得る。このときの延伸温度は、原料レジンのガラス転移温度(Tg)のマイナス10℃からプラス40℃の温度範囲で延伸する。また、延伸倍率は、好ましくは2.5〜7.0倍、さらに好ましくは3.0〜6.0倍である。さらに、縦延伸を一段階のみで行ってもよいし、二段階以上に分けて行ってもよい。次いで、易接着層を設けるためコーターにより水性塗布剤を塗布する。その後、テンターに導きテンター延伸機を用いて、一軸延伸フィルムをその幅方向に延伸(横延伸)することにより二軸延伸フィルムを得る。このときの延伸温度は、原料レジンのガラス転移温度(Tg)からプラス50℃の温度範囲で延伸する。また、延伸倍率は、好ましくは2.5〜7.0倍、さらに好ましくは3.5〜6.0倍である。さらに、横延伸を一段階のみで行ってもよいし、二段以上に分けて行ってもよい。また縦と横を同時に行う同時二軸延伸を行ってもよい。そして二軸延伸フィルムを熱処理することにより積層フィルムが製造される。このときの熱処理温度は、130〜250℃である。二軸延伸フィルムを熱処理するときには、二軸延伸フィルムに対して20%以内の弛緩を行ってもよい。   When the film of the present invention is produced, the dried polyester is supplied to an extruder and heated to a temperature equal to or higher than the melting point of each polyester to be melted. Subsequently, it extrudes from a T die as a molten sheet through a pump and a filter. Subsequently, the molten sheet is rapidly cooled to below the glass transition temperature on a rotary cooling drum to obtain an amorphous unstretched film. At this time, in order to improve the flatness of the unstretched film, the adhesion between the unstretched film and the rotating cooling drum may be improved by an electrostatic application adhesion method, a liquid application adhesion method, or the like. And a uniaxially stretched film is obtained by extending | stretching an unstretched film in the longitudinal direction (longitudinal stretching) using a roll stretching machine. The stretching temperature at this time is stretched in a temperature range of minus 10 ° C. to plus 40 ° C. of the glass transition temperature (Tg) of the raw material resin. The draw ratio is preferably 2.5 to 7.0 times, more preferably 3.0 to 6.0 times. Furthermore, longitudinal stretching may be performed in only one stage, or may be performed in two or more stages. Next, an aqueous coating agent is applied by a coater to provide an easy adhesion layer. Then, it leads to a tenter and a biaxially stretched film is obtained by extending | stretching a uniaxially stretched film in the width direction (lateral stretching) using a tenter stretching machine. The stretching temperature at this time is stretched in a temperature range of + 50 ° C. from the glass transition temperature (Tg) of the raw material resin. The draw ratio is preferably 2.5 to 7.0 times, more preferably 3.5 to 6.0 times. Further, the transverse stretching may be performed only in one stage, or may be performed in two or more stages. Moreover, you may perform simultaneous biaxial stretching which performs vertical and horizontal simultaneously. And a laminated film is manufactured by heat-processing a biaxially stretched film. The heat processing temperature at this time is 130-250 degreeC. When the biaxially stretched film is heat-treated, the biaxially stretched film may be relaxed within 20%.

本発明によれば、フィルターの圧力上昇が小さいため生産性に優れ、艶消し性および光散乱性に優れた易接着二軸延伸ポリエステルフィルムを提供することができ、本発明の工業的価値は高い。   ADVANTAGE OF THE INVENTION According to this invention, since the pressure rise of a filter is small, it is excellent in productivity, can provide the easily-adhesive biaxially-stretched polyester film excellent in the matte property and the light-scattering property, The industrial value of this invention is high. .

以下、本発明を実施例によりさらに詳細に説明するが、本発明はその要旨を越えない限り、以下の実施例に限定されるものではない。なお、実施例および本発明で用いた測定法および用語の定義は次のとおりである。   EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not limited to a following example, unless the summary is exceeded. The measurement methods and terms used in the examples and the present invention are defined as follows.

(1)添加粒子平均粒子径
電子顕微鏡を用いて粒子を観察して最大径と最小径を求め、その平均を粒子1個の粒径とした。フィルム中の少なくとも100個の粒子についてこれを行う。粒子群の平均粒子径は、これらの粒子の重量平均径とする。
(1) Added particle average particle diameter The particles were observed using an electron microscope to determine the maximum diameter and the minimum diameter, and the average was defined as the particle diameter of one particle. This is done for at least 100 particles in the film. The average particle diameter of the particle group is the weight average diameter of these particles.

(2)変形度
フィルム小片をエポキシ樹脂にて固定成形した後、フィルム切断面が分子鎖配向の主軸方向と平行になるようにミクロトームで切断し、切断面を走査型電子顕微鏡にて観察する。粒子毎に平均粒径の±10%に入る少なくとも50個の粒子について、最大径と最小径の比を算出し、その相加平均を変形度とする。
(2) Deformation After fixing the film piece with an epoxy resin, it is cut with a microtome so that the cut surface of the film is parallel to the principal axis direction of the molecular chain orientation, and the cut surface is observed with a scanning electron microscope. For at least 50 particles that fall within ± 10% of the average particle size for each particle, the ratio of the maximum diameter to the minimum diameter is calculated, and the arithmetic average is taken as the degree of deformation.

(3)光沢度
JIS Z−8741−1983の方法3(60゜光沢度)によって、単層フィルム表面もしくはA層表面のフィルムの縦延伸方向に光を入射して測定する。
(3) Glossiness Measured by incident light in the longitudinal stretching direction of the film on the surface of the single-layer film or the surface of the A-layer according to method 3 (60 ° glossiness) of JIS Z-8741-1983.

(4)有機粒子の熱分解温度
有機粒子を60℃で4時間減圧乾燥後、窒素ガス雰囲気下、昇温速度20℃/分の条件で熱天秤(理学電気社、TAS100型)を用いて測定した5%減量時点の温度を測定する。
(4) Thermal decomposition temperature of organic particles After drying the organic particles under reduced pressure at 60 ° C. for 4 hours, measurement was performed using a thermobalance (Rigaku Denki Co., Ltd., TAS100 type) under a nitrogen gas atmosphere at a temperature rising rate of 20 ° C./min. Measure the temperature at the time of 5% weight loss.

(5)フィルター圧力上昇
捕集効率が20μm捕集径で50から60%のフィルターを用いて、フィルム製造時の前に粒子含有量2wt%のレジンを吐出量20kg/hで押し出し、フィルター手前の樹脂の圧力を測定する。1時間で圧力差が0.5メガパスカルを超えた場合は、フィルター寿命が不合格(×)、0.5メガパスカル以下の場合は合格(○)とする。
(5) Increase in filter pressure Using a filter with a collection efficiency of 20 μm and a collection diameter of 50 to 60%, extrude a resin with a particle content of 2 wt% at a discharge rate of 20 kg / h before the film production. Measure the pressure of the resin. If the pressure difference exceeds 0.5 megapascals in 1 hour, the filter life is rejected (x), and if it is 0.5 megapascals or less, it is passed (o).

(6)光散乱性
蛍光灯下の机にMSゴシックの書体で大きさが8ポイントの1から9の数字を印刷した紙を置き、試験フィルムを通して30cmの距離から観察して、数字が判別できなくなるフィルムと紙の間の距離を測定する。光散乱性は以下のように評価する。
○:数字が見えなくなる距離が5cm以下であり、光散乱性が良好
×:数字が見えなくなる距離が5cmを超え、光散乱性が不良
(6) Light-scattering properties Place a paper with MS Gothic font printed with numbers 1 to 9 with 8 points on a desk under a fluorescent lamp, and observe the distance from a distance of 30 cm through the test film. Measure the distance between the missing film and the paper. The light scattering property is evaluated as follows.
○: The distance at which the numbers cannot be seen is 5 cm or less, and the light scattering property is good. X: The distance at which the numbers cannot be seen exceeds 5 cm, and the light scattering property is poor.

(7)光硬化性樹脂との接着性
易接着面の表面にアクリル系光硬化樹脂(日本化薬製KAYANOVA FOP−1700)を硬化後の厚さが6μmになるように塗布し、120W/cmのエネルギーの高圧水銀灯を使用し、照射距離100mmにて約10秒間照射して、表面硬化フィルムを得る。アクリル系光硬化層形成直後、当該層に1インチ幅に碁盤目が100個になるようクロスカットを入れ、直ちに、同一箇所について3回セロテープ(登録商標)急速剥離テストを実施し、剥離面積により評価する。判定基準は以下のとおりである。
◎:碁盤目剥離個数=0
○:1≦碁盤目剥離個数≦10
△:11≦碁盤目剥離個数≦20
×:21<碁盤目剥離個数
(7) Adhesiveness with photo-curing resin An acrylic photo-curing resin (KAYANOVA FOP-1700 manufactured by Nippon Kayaku Co., Ltd.) was applied to the surface of the easy-adhesion surface so that the thickness after curing was 6 μm, and 120 W / cm. A surface-cured film is obtained by irradiating at an irradiation distance of 100 mm for about 10 seconds using a high-pressure mercury lamp having the following energy. Immediately after the acrylic photocured layer is formed, a crosscut is made on the layer so that there are 100 grids in a 1-inch width, and a cellotape (registered trademark) rapid peel test is performed three times at the same location. evaluate. The judgment criteria are as follows.
A: Number of cross-cuts = 0
○: 1 ≦ Number of cross cuts ≦ 10
Δ: 11 ≦ number of cross-cuts ≦ 20
×: 21 <Number of cross-cuts peeled

(8)フィルム透過光の品位
分光光度計UV−3100PC(島津製作所(株)製)を用いて波長800nmから300nmまでの光線透過率%を測定し、波長750nmと400nmの光線透過率%の差を求める。
○:波長750nmと400nmの光線透過率の差が15%以下であり、品位良好
△:波長750nmと400nmの光線透過率の差が15〜20%であり、やや品位が劣る
×:波長750nmと400nmの光線透過率の差が20%を超え、品位が劣る
(8) Quality of film transmitted light Using a spectrophotometer UV-3100PC (manufactured by Shimadzu Corporation), the light transmittance% from a wavelength of 800 nm to 300 nm was measured, and the difference between the light transmittance% at a wavelength of 750 nm and 400 nm. Ask for.
○: The difference in light transmittance between wavelengths 750 nm and 400 nm is 15% or less, and the quality is good. △: The difference in light transmittance between wavelengths 750 nm and 400 nm is 15 to 20%, and the quality is slightly inferior. The difference in light transmittance at 400nm exceeds 20% and the quality is inferior

(原料の調整)
・ポリエステルa
常法の重縮合で合成された極限粘度0.65、融点253℃のポリエチレンテレフタレートである。
(Raw material adjustment)
・ Polyester a
Polyethylene terephthalate having an intrinsic viscosity of 0.65 and a melting point of 253 ° C. synthesized by a conventional polycondensation.

・ポリエステルb
常法の重縮合で合成された極限粘度0.68、融点253℃のポリエチレンテレフタレート樹脂に平均粒径6μm、5%熱分解温度が329℃の粒子表面に水酸基を有する架橋スチレン-アクリル有機粒子を練り込み4.0重量%含有させたものである。
・ Polyester b
Crosslinked styrene-acrylic organic particles having a hydroxyl group on the surface of a polyethylene terephthalate resin having an intrinsic viscosity of 0.68 and a melting point of 253 ° C. synthesized by a conventional polycondensation and having an average particle size of 6 μm and a thermal decomposition temperature of 329 ° C. Kneaded 4.0% by weight.

・ポリエステルc
常法の重縮合で合成された極限粘度0.68、融点253℃のポリエチレンテレフタレート樹脂に平均粒径10μm、5%熱分解温度が331℃の粒子表面にグリシジル基を有する架橋スチレン-アクリル有機粒子を練り込み8.0重量%含有させたものである。
・ Polyester c
Crosslinked styrene-acrylic organic particles having a glycidyl group on the surface of a polyethylene terephthalate resin synthesized by a conventional polycondensation having an intrinsic viscosity of 0.68 and a melting point of 253 ° C., an average particle size of 10 μm, and a 5% thermal decomposition temperature of 331 ° C. Is kneaded and contained at 8.0% by weight.

・ポリエステルd
常法の重縮合で合成された極限粘度0.68、融点253℃のポリエチレンテレフタレート樹脂に平均粒径10μm、粒子表面に水酸基を有する球状多孔質シリカ粒子を練り込み4.0重量%含有させたものである。
・ Polyester d
Spherical porous silica particles having an average particle size of 10 μm and a hydroxyl group on the particle surface were kneaded into a polyethylene terephthalate resin having an intrinsic viscosity of 0.68 and a melting point of 253 ° C. synthesized by a conventional polycondensation to contain 4.0% by weight. Is.

・ポリエステルe
常法の重縮合で合成された極限粘度0.68、融点253℃のポリエチレンテレフタレート樹脂に平均粒径1.7μm、粒子表面にカルボン酸基を有する5%熱分解温度が290℃の架橋アクリル有機粒子を練り込み2.0重量%含有させたものである。
・ Polyester e
Cross-linked acrylic organic having an intrinsic viscosity of 0.68 synthesized by a conventional polycondensation, a polyethylene terephthalate resin having a melting point of 253 ° C., an average particle diameter of 1.7 μm, a 5% thermal decomposition temperature of 290 ° C. having a carboxylic acid group on the particle surface Particles are kneaded and contained at 2.0% by weight.

水性塗布剤A
水性塗布剤は下記a、b、c、dの化合物を47/20/30/3の重量比で混合した混合物である。
a:テレフタル酸/イソフタル酸/5−ソジウムスルホイソフタル酸/エチレングリコール/1.4−ブタンジオール/ジエチレングリコールを各々28/20/2/35/10/5のモル比で反応させたポリエステル水分散体
b:メチルメタクリレート/エチルアクリレート/アクリロニトリル/N−メチロールメタアクリルアミドを各々45/45/5/5のモル比で重合された重合物水分散体(乳化剤:アニオン系界面活性剤)
c:メラミン系架橋剤(ヘキサメトキシメチルメラミン)
d:平均粒径0.06μmの酸化ケイ素の水分散体
Aqueous coating agent A
The aqueous coating agent is a mixture in which the following compounds a, b, c and d are mixed at a weight ratio of 47/20/30/3.
a: Polyester aqueous dispersion obtained by reacting terephthalic acid / isophthalic acid / 5-sodiumsulfoisophthalic acid / ethylene glycol / 1.4-butanediol / diethylene glycol in a molar ratio of 28/20/2/35/10/5, respectively Body b: Polymer aqueous dispersion obtained by polymerizing methyl methacrylate / ethyl acrylate / acrylonitrile / N-methylol methacrylamide in a molar ratio of 45/45/5/5 (emulsifier: anionic surfactant)
c: Melamine-based crosslinking agent (hexamethoxymethyl melamine)
d: An aqueous dispersion of silicon oxide having an average particle size of 0.06 μm

実施例1:
ポリエステルaが50重量%とポリエステルbが50重量%の混合物をベント付き2軸押出機に供給し、溶融温度280℃で溶融したあとポンプとフィルターを介してダイを通してキャスティングドラムに引き取り単層未延伸フィルムを得た。かくして得られた未延伸フィルムを縦延伸ロールに送り込み、まずフィルム温度83℃で3.7倍延伸した後、片面に水性塗布剤Aを塗布し、テンターに導き95℃で横方向に4.0倍延伸して二軸配向フィルムを得た。次いで、得られた二軸配向フィルムを熱固定ゾーンに導き、230℃で5秒間幅方向に3%弛緩させながら熱固定し、下記表1に記載する厚みのポリエステルフィルムを得た。
Example 1:
A mixture of 50% by weight of polyester a and 50% by weight of polyester b is fed to a twin-screw extruder with a vent, melted at a melting temperature of 280 ° C., taken through a die through a pump and a filter, and then drawn into a casting drum. A film was obtained. The unstretched film thus obtained was fed into a longitudinal stretching roll and first stretched 3.7 times at a film temperature of 83 ° C., and then an aqueous coating agent A was applied on one side, led to a tenter, and 4.0 sideways at 95 ° C. The film was stretched twice to obtain a biaxially oriented film. Next, the obtained biaxially oriented film was introduced into a heat setting zone, and heat-set while being relaxed by 3% in the width direction at 230 ° C. for 5 seconds to obtain a polyester film having a thickness described in Table 1 below.

実施例2:
中間層(B層)を構成するポリエステルaが87.5重量%とポリエステルcが12.5重量%の混合物をベント付き2軸押出機(メイン)に供給し、表層(A層)を形成するポリエステルaを別のベント付き2軸押出機(サブ)に供給して溶融温度280℃で溶融したあと、各押出機からの溶融ポリマーをギヤポンプとフィルターを介してフィードブロックで合流させ、ダイを通してキャスティングドラムに引き取り2種3層の未延伸フィルムを得た。その後は実施例1と同じく、片面に水性塗布剤Aを塗布し、テンターに導き延伸し熱固定し、表1に記載する厚み構成のフィルムを得た。
Example 2:
A mixture of 87.5% by weight of polyester a constituting the intermediate layer (B layer) and 12.5% by weight of polyester c is supplied to a vented twin-screw extruder (main) to form a surface layer (A layer). Polyester a is fed to another twin-screw extruder with a vent (sub) and melted at a melting temperature of 280 ° C., then the molten polymer from each extruder is merged with a feed block through a gear pump and a filter, and cast through a die. It was taken up on a drum to obtain an unstretched film of 2 types and 3 layers. Thereafter, as in Example 1, aqueous coating agent A was applied on one side, led to a tenter, stretched and heat-fixed to obtain a film having a thickness structure described in Table 1.

実施例3:
表層(A層)を形成するポリエステルaが67.5重量%とポリエステルbが32.5重量%の混合物をベント付き2軸押出機(サブ)に供給し、中間層(B層)を構成するポリエステルaを別のベント付き2軸押出機(メイン)に供給して溶融温度280℃で溶融したあと、各押出機からの溶融ポリマーをギヤポンプとフィルターを介してフィードブロックで合流させ、ダイを通してキャスティングドラムに引き取り2種3層の未延伸フィルムを得た。その後は実施例1と同じく、片面に水性塗布剤Aを塗布し、テンターに導き延伸し熱固定し表1に記載する厚み構成のフィルムを得た。
Example 3:
A mixture of 67.5% by weight of polyester a forming the surface layer (A layer) and 32.5% by weight of polyester b is fed to a twin-screw extruder with a vent (sub) to form an intermediate layer (B layer) Polyester a is fed to another twin-screw extruder with a vent (main) and melted at a melting temperature of 280 ° C., then the molten polymer from each extruder is merged with a feed block through a gear pump and a filter, and cast through a die. It was taken up on a drum to obtain an unstretched film of 2 types and 3 layers. Thereafter, as in Example 1, aqueous coating agent A was applied on one side, led to a tenter, stretched and heat-fixed to obtain a film having a thickness structure described in Table 1.

比較例1:
フィルムを作成する前に、ポリエステルdが50重量%とポリエステルaが50重量%の混合物を用いてフィルター圧力上昇テストを行ったところ、圧力上昇が認められたため、フィルムの作成は実施しなかった。
Comparative Example 1:
Before forming a film, a filter pressure increase test was conducted using a mixture of 50% by weight of polyester d and 50% by weight of polyester a. As a result, a pressure increase was observed, so that no film was prepared.

比較例2:
易接着層を設けなかったほかは実施例1と同じ条件でフィルムを得た。
Comparative Example 2:
A film was obtained under the same conditions as in Example 1 except that the easy adhesion layer was not provided.

比較例3:
表層(A層)を形成するポリエステルe100重量%をベント付き2軸押出機(サブ)に供給し、中間層(B層)を構成するポリエステルaを別のベント付き2軸押出機(メイン)に供給したほか実施例3と同様にして下記表2に記載した厚み構成のフィルムを得た。
Comparative Example 3:
100% by weight of polyester e forming the surface layer (A layer) is supplied to a biaxial extruder with a vent (sub), and polyester a constituting the intermediate layer (B layer) is supplied to another biaxial extruder with a vent (main) A film having a thickness structure described in Table 2 below was obtained in the same manner as in Example 3 except that the film was supplied.

比較例4:
表層(A層)を形成するポリエステルaが85重量%とポリエステルbが15重量%の混合物をベント付き2軸押出機(サブ)に供給し、中間層(B層)を構成するポリエステルaを別のベント付き2軸押出機(メイン)に供給したほか実施例3と同様にして表2に記載する厚み構成のフィルムを得た。
以上、得られた結果をまとめて下記表1および2に示す。
Comparative Example 4:
A mixture of 85% by weight of polyester a forming the surface layer (A layer) and 15% by weight of polyester b is supplied to a twin-screw extruder with a vent (sub), and the polyester a constituting the intermediate layer (B layer) is separated. In the same manner as in Example 3 except that the film was supplied to a vented twin-screw extruder (main), a film having a thickness structure described in Table 2 was obtained.
The obtained results are summarized in Tables 1 and 2 below.

Figure 2007125824
Figure 2007125824

Figure 2007125824
Figure 2007125824

実施例1〜3においては、フィルターの圧力上昇がなく生産に優れ、フィルムの易接着性、艶消し性や光散乱性に優れる。一方、比較例1は、無機粒子を用いているためフィルターの圧力上昇が観察された。比較例2は、易接着塗布層がないため、アクリル系光硬化樹脂と接着性が劣った。比較例3は、平均粒子径の大きさが2.0μm未満のため、光散乱性に劣った。また有機粒子の耐熱性が300℃未満のため透過光の品位が低下した。比較例4は、有機粒子の濃度が0.10重量%濃度よりも小さいため、光散乱性や艶消し効果がなかった。   In Examples 1 to 3, there is no increase in the pressure of the filter, the production is excellent, and the easy adhesion, matting and light scattering properties of the film are excellent. On the other hand, since the comparative example 1 used the inorganic particle, the pressure rise of the filter was observed. Since Comparative Example 2 did not have an easy-adhesion coating layer, the adhesiveness with the acrylic photocurable resin was inferior. Comparative Example 3 was inferior in light scattering property because the average particle size was less than 2.0 μm. Moreover, since the heat resistance of the organic particles was less than 300 ° C., the quality of transmitted light was reduced. In Comparative Example 4, since the concentration of the organic particles was smaller than 0.10% by weight, there was no light scattering property or matting effect.

本発明のフィルムは、例えば、ポリエステルフィルムの表面に接着剤層や紫外線硬化樹脂層などを設けて使用される、艶消し性が必要とされるガラスや成形体貼り合わせ用途や包装用途、また液晶ディスプレイの構成部品、例えばプリズムシートや光拡散シートの基材フィルムとして好適に利用することができる。   The film of the present invention is used, for example, by providing an adhesive layer or an ultraviolet curable resin layer on the surface of a polyester film. It can be suitably used as a base film of a display component, for example, a prism sheet or a light diffusion sheet.

Claims (1)

少なくとも片面に易接着塗布層を有する二軸延伸ポリエステルフィルムであって、5%熱分解温度が300℃以上であり、平均粒子径が2.0〜40μmの有機粒子を0.10〜10重量%含有することを特徴とする二軸延伸ポリエステルフィルム。 A biaxially stretched polyester film having an easy-adhesion coating layer on at least one surface, having 5% pyrolysis temperature of 300 ° C. or higher and 0.10-10% by weight of organic particles having an average particle size of 2.0-40 μm A biaxially stretched polyester film characterized by containing.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007146056A (en) * 2005-11-29 2007-06-14 Mitsubishi Polyester Film Copp Light scattering biaxially-oriented polyester film
JP2010173084A (en) * 2009-01-27 2010-08-12 Mitsubishi Plastics Inc Biaxially oriented laminated polyester film
JP2012092169A (en) * 2010-10-25 2012-05-17 Mitsubishi Plastics Inc Laminated polyester film
JP2013047356A (en) * 2012-12-07 2013-03-07 Mitsubishi Plastics Inc Light scattering biaxially oriented polyester film
KR101848452B1 (en) * 2016-03-21 2018-04-13 에스케이씨 주식회사 Multilayer white porous polyester film

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Publication number Priority date Publication date Assignee Title
JPS595216A (en) * 1982-06-30 1984-01-12 Fujitsu Ltd Optical fiber connector
JPH07304938A (en) * 1994-05-11 1995-11-21 Toray Ind Inc Biaxially oriented laminated polyester film
JPH07323511A (en) * 1994-06-02 1995-12-12 Toray Ind Inc Laminated polyester film
JP2001322218A (en) * 2000-05-16 2001-11-20 Mitsubishi Polyester Film Copp Coextrusion laminated polyester film
JP2002220487A (en) * 2001-01-26 2002-08-09 Toppan Printing Co Ltd Hard coat film

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS595216A (en) * 1982-06-30 1984-01-12 Fujitsu Ltd Optical fiber connector
JPH07304938A (en) * 1994-05-11 1995-11-21 Toray Ind Inc Biaxially oriented laminated polyester film
JPH07323511A (en) * 1994-06-02 1995-12-12 Toray Ind Inc Laminated polyester film
JP2001322218A (en) * 2000-05-16 2001-11-20 Mitsubishi Polyester Film Copp Coextrusion laminated polyester film
JP2002220487A (en) * 2001-01-26 2002-08-09 Toppan Printing Co Ltd Hard coat film

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007146056A (en) * 2005-11-29 2007-06-14 Mitsubishi Polyester Film Copp Light scattering biaxially-oriented polyester film
JP2010173084A (en) * 2009-01-27 2010-08-12 Mitsubishi Plastics Inc Biaxially oriented laminated polyester film
JP2012092169A (en) * 2010-10-25 2012-05-17 Mitsubishi Plastics Inc Laminated polyester film
JP2013047356A (en) * 2012-12-07 2013-03-07 Mitsubishi Plastics Inc Light scattering biaxially oriented polyester film
KR101848452B1 (en) * 2016-03-21 2018-04-13 에스케이씨 주식회사 Multilayer white porous polyester film

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