JP2005008891A - Crosslinked polymer and medical sheet comprising the polymer - Google Patents

Crosslinked polymer and medical sheet comprising the polymer Download PDF

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JP2005008891A
JP2005008891A JP2004204885A JP2004204885A JP2005008891A JP 2005008891 A JP2005008891 A JP 2005008891A JP 2004204885 A JP2004204885 A JP 2004204885A JP 2004204885 A JP2004204885 A JP 2004204885A JP 2005008891 A JP2005008891 A JP 2005008891A
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sheet
resin
crosslinked polymer
polytransisoprene
polymer
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JP3714629B2 (en
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Ichiji Watanabe
一司 渡辺
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Daicel Corp
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a crosslinked polymer having proper viscoelasticities in molten state and in solid state respectively and useful as a material of a sheet for radiation therapy, a sheet for plaster cast, a patterning sheet for wig, tooth or the like. <P>SOLUTION: The crosslinked polymer is obtained by irradiating a polytransisoprene resin or an ethylenic copolymer resin each having a melting point of 40-80°C with active energy rays to cause crosslinking. The medical sheet comprises the crosslinked polymer. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

本発明は、活性エネルギー線照射による架橋重合体およびこの架橋重合体から成る医療用シートに関する。より詳しくは、比較的低温で適切な粘弾性を有する活性エネルギー線照射による架橋重合体ならびにこの架橋重合体から成る放射線治療用シート、ギブス用シートおよびかつらまたは歯の型取り用シートに関する。   The present invention relates to a cross-linked polymer by irradiation with active energy rays and a medical sheet comprising the cross-linked polymer. More specifically, the present invention relates to a crosslinked polymer by irradiation with active energy rays having appropriate viscoelasticity at a relatively low temperature, and a radiation treatment sheet, a cast sheet, and a wig or tooth mold sheet made of the crosslinked polymer.

ポリカプロラクトンやポリイソプレン等の融点(軟化点)が40〜80℃の範囲である熱可塑性樹脂は、比較的低い温度で容易に溶融し、外力を加えると容易に変形させることができ、冷却固化すると強靭である性質を生かしてギブスやかつら、歯等の型取りシートに利用されている。   Thermoplastic resins having a melting point (softening point) such as polycaprolactone and polyisoprene in the range of 40 to 80 ° C. can be easily melted at a relatively low temperature, and can be easily deformed by applying external force, and cooled and solidified. Then, taking advantage of its toughness, it is used for casting sheets such as casts, wigs and teeth.

しかしながら、これらの樹脂の溶融状態における粘性は低く、弾性は無いことから、「タレ」が発生したり、過剰な外力を加えると破断したり、一旦変形すると元の形には戻らない欠点がある。   However, since the viscosity of these resins in the molten state is low and there is no elasticity, there is a drawback that “sag” occurs, breaks when excessive external force is applied, or does not return to its original shape once deformed. .

本発明者は、検討の結果、低融点熱可塑性樹脂に活性エネルギー線を照射して架橋反応を起こすことによって得られる樹脂が溶融状態におけるゴム弾性や形状記憶性を有すること、更にこの樹脂を種々の医療用シートに用いると、「タレ」やシートの破断を発生せず、自由自在にシートを型作ることができることを見い出し、本発明に至った。   As a result of the study, the present inventor has found that the resin obtained by irradiating a low melting point thermoplastic resin with an active energy ray to cause a crosslinking reaction has rubber elasticity and shape memory property in a molten state, and various other resins. As a result, the inventors have found that the sheet can be freely formed without causing “sagging” or sheet breakage, and the present invention has been achieved.

すなわち、本発明は融点が40〜80℃であるポリトランスイソプレン系樹脂またはエチレン系共重合樹脂に活性エネルギー線を照射して架橋反応を起こすことにより得られることを特徴とする架橋重合体を提供する。   That is, the present invention provides a crosslinked polymer obtained by irradiating an active energy ray to a polytransisoprene resin or ethylene copolymer resin having a melting point of 40 to 80 ° C. to cause a crosslinking reaction. To do.

また、本発明は上記架橋重合体から成ることを特徴とする放射線治療用シート、ギブス用シートおよびかつらまたは歯の型取り用シートを提供する。   The present invention also provides a radiation treatment sheet, a cast sheet, and a wig or tooth shaping sheet comprising the above-mentioned crosslinked polymer.

本発明の架橋重合体は、比較的低温で溶融し、溶融時および固化時においてそれぞれ適切な粘弾性を有しているので、放射線治療用シート、ギブス用シートおよびかつらまたは歯の型取り用シートなどの材料として有用である。   Since the crosslinked polymer of the present invention is melted at a relatively low temperature and has appropriate viscoelasticity at the time of melting and solidifying, a radiation treatment sheet, a cast sheet, and a wig or tooth mold sheet It is useful as a material.

本発明における融点が40〜80℃であるポリトランスイソプレン系樹脂またはエチレン系共重合樹脂としては、ポリトランスイソプレン系樹脂およびエチレン−酢酸ビニル、エチレン−塩化ビニル、エチレン−ビニルアルコール(エチレン−酢酸ビニル共重合体のケン化物)およびエチレン−プロピレン系共重合体等の内、融点が40〜80℃の樹脂であれば、いかなる樹脂も使用できる。共重合成分が10〜40モル%の割合が、通常、融点が40〜80℃の範囲にあり、好ましい。   Examples of the polytransisoprene resin or ethylene copolymer resin having a melting point of 40 to 80 ° C. in the present invention include polytransisoprene resin, ethylene-vinyl acetate, ethylene-vinyl chloride, ethylene-vinyl alcohol (ethylene-vinyl acetate). Any resin can be used as long as it has a melting point of 40 to 80 ° C. among the saponified copolymer) and the ethylene-propylene copolymer. A proportion of 10 to 40 mol% of the copolymer component is usually preferable because the melting point is in the range of 40 to 80 ° C.

ポリトランスイソプレン系樹脂およびエチレン系共重合樹脂は現在商業的スケールで製造されており、好ましく使用できる。エチレン系共重合樹脂は、結晶性を有しているが、透明性に優れ、かつら型取り材等の型取りシートのうち透明性が必要とされる用途の場合に好ましく用いられる。   Polytransisoprene resins and ethylene copolymer resins are currently produced on a commercial scale and can be preferably used. The ethylene-based copolymer resin has crystallinity, but is excellent in transparency, and is preferably used in applications where transparency is required in a mold sheet such as a wig mold material.

上記の融点が40〜80℃であるポリトランスイソプレン系樹脂またはエチレン系共重合樹脂の数平均分子量は、通常、10,000〜300,000、好ましくは40,000〜200,000、更に好ましくは60,000〜150,000の範囲である。   The number average molecular weight of the polytransisoprene resin or ethylene copolymer resin having a melting point of 40 to 80 ° C. is usually 10,000 to 300,000, preferably 40,000 to 200,000, more preferably. It is in the range of 60,000 to 150,000.

上記分子量が10,000未満の場合は、各種成形品を製造することが困難であり、製造されたものの機械的強度は著しく低くなる傾向があり、逆に300,000を上回る場合には溶融粘度が高すぎて、成形加工性が低減する傾向があるため好ましくない。   When the molecular weight is less than 10,000, it is difficult to produce various molded products, and the mechanical strength of the produced products tends to be remarkably lowered. Conversely, when the molecular weight exceeds 300,000, the melt viscosity Is too high, and there is a tendency for molding processability to decrease, which is not preferable.

また融点が40〜80℃である理由としては、40℃未満のものから得られる架橋重合体では夏時期の貯蔵が困難であったり、固定用シートとして使用したとき、室温においても、なかなか固化しないため使用が困難であったりし、逆に80℃を上回るものから得られる架橋重合体の場合には、溶融した樹脂が熱いため、人体に置くことができず適当でない。   The reason why the melting point is 40 to 80 ° C. is that it is difficult to store in the summer in a crosslinked polymer obtained from a temperature lower than 40 ° C., and when used as a fixing sheet, it does not solidify easily even at room temperature. Therefore, it is difficult to use, and in the case of a cross-linked polymer obtained from a polymer having a temperature higher than 80 ° C., the molten resin is hot and cannot be placed on the human body.

本発明の好ましい態様では、融点が40〜80℃であるポリトランスイソプレン系樹脂またはエチレン系共重合樹脂に多官能アクリル単量体および多官能アリル単量体を添加する。これらの単量体としては、特に限定はなく、多官能アクリル単量体の例としては、エチレンオキサイド変性ビスフェノールAジ(メタ)アクリレート、1,4−ブタンジオールジ(メタ)アクリレート、ジエチレングリコールジ(メタ)アクリレート、ジペンタエリスリトールヘキサアクリレート、ジペンタエリスリトールモノヒドロキシペンタアクリレート、カプロラクトン変性ジペンタエリスリトールヘキサアクリレート、ペンタエリスリトールトリアクリレート、ペンタエリスリトールテトラアクリレート、ポリエチレングリコールジ(メタ)アクリレート、トリメチロールプロパントリアクリレート、エチレンオキサイド変性トリメチロールプロパントリアクリレート、プロピレンオキサイド変性トリメチロールプロパントリアクリレート、トリス(アクリロキシエチル)イソシアヌレート、トリス(メタクリロキシエチル)イソシアヌレートおよびこれらの混合物が、多官能アリル系単量体の例としては、トリアリルシアヌレート、トリアリルイソシアヌレートジアリルフタレート、ジアリルベンゼンホスフォネートおよびこれらの混合物等が挙げられる。   In a preferred embodiment of the present invention, a polyfunctional acrylic monomer and a polyfunctional allyl monomer are added to a polytransisoprene resin or ethylene copolymer resin having a melting point of 40 to 80 ° C. These monomers are not particularly limited, and examples of polyfunctional acrylic monomers include ethylene oxide-modified bisphenol A di (meth) acrylate, 1,4-butanediol di (meth) acrylate, diethylene glycol di ( (Meth) acrylate, dipentaerythritol hexaacrylate, dipentaerythritol monohydroxypentaacrylate, caprolactone-modified dipentaerythritol hexaacrylate, pentaerythritol triacrylate, pentaerythritol tetraacrylate, polyethylene glycol di (meth) acrylate, trimethylolpropane triacrylate, Ethylene oxide modified trimethylolpropane triacrylate, propylene oxide modified trimethylolpropane triacrylate Examples of polyfunctional allylic monomers include triallyl cyanurate, triallyl isocyanurate diallyl phthalate, tris (acryloxyethyl) isocyanurate, tris (methacryloxyethyl) isocyanurate and mixtures thereof. Examples include diallylbenzene phosphonate and a mixture thereof.

これらの多官能アクリル単量体または多官能アリル単量体は、ポリトランスイソプレン系樹脂およびエチレン系共重合樹脂100重量部に対して、0.1〜30重量部、好ましくは0.3〜10重量部、更に好ましくは0.5〜5重量部の範囲で混合される。上記量が0.1重量部未満の場合は、架橋重合体の形状記憶性等が満足できるレベルではなく、逆に30重量部を上回る場合には、架橋重合体が剛直になりすぎて、靭性が低下する傾向があるため好ましくない。   These polyfunctional acrylic monomers or polyfunctional allyl monomers are used in an amount of 0.1 to 30 parts by weight, preferably 0.3 to 10 parts by weight based on 100 parts by weight of the polytransisoprene resin and the ethylene copolymer resin. Part by weight, more preferably in the range of 0.5 to 5 parts by weight. When the amount is less than 0.1 parts by weight, the shape memory property of the crosslinked polymer is not at a satisfactory level. Conversely, when the amount exceeds 30 parts by weight, the crosslinked polymer becomes too rigid and toughness Is not preferable because of a tendency to decrease.

活性エネルギー線としては、その波長や、エネルギー量に特に限定はないが、電子線(EB)が一般的である。これらの活性エネルギー線は、公知の装置を用いて照射できる。照射線量は、熱可塑性樹脂に架橋を生じさせるのに十分な量が適宜選択される。例えば、電子線(EB)の場合の加速電圧としては100〜300KV、吸収線量としては、0.1〜30Mradの範囲が適当である。   The active energy ray is not particularly limited in wavelength and energy amount, but an electron beam (EB) is common. These active energy rays can be irradiated using a known apparatus. The irradiation dose is appropriately selected as an amount sufficient to cause crosslinking in the thermoplastic resin. For example, in the case of an electron beam (EB), an acceleration voltage of 100 to 300 KV and an absorbed dose of 0.1 to 30 Mrad are appropriate.

これらの活性エネルギー線を照射する場合、融点が40〜80℃である熱可塑性樹脂の形態については、特に限定はないが、厚さ10μm〜5mmの範囲内のフィルムまたはシートが照射効率が高いため使用し易い。特に厚さ0.5mm〜3mm程度のシートは放射線治療用シート、ギブス用シート、かつらまたは歯の型取り用シート等の医療用シートとして使用できるため好ましく用いられる。   When irradiating these active energy rays, there is no particular limitation on the form of the thermoplastic resin having a melting point of 40 to 80 ° C., but a film or sheet having a thickness of 10 μm to 5 mm has high irradiation efficiency. Easy to use. In particular, a sheet having a thickness of about 0.5 mm to 3 mm is preferably used because it can be used as a medical sheet such as a radiation treatment sheet, a cast sheet, a wig, or a tooth shaping sheet.

また本発明の架橋重合体に対しては、使用用途によって任意の物質を適当な時期に混合または塗布することができる。   In addition, any substance can be mixed or applied to the crosslinked polymer of the present invention at an appropriate time depending on the intended use.

上記物質としては、ガラス繊維、ガラスビーズ、金属粉末、タルク、マイカ、シリカ等の無機充填剤、顔料、各種安定剤、難燃剤、帯電防止剤、防カビ剤、可塑剤、粘性付与剤等の添加剤、熱可塑性樹脂および硬化性オリゴマー等が例示できる。   Examples of the substances include inorganic fillers such as glass fiber, glass beads, metal powder, talc, mica, and silica, pigments, various stabilizers, flame retardants, antistatic agents, antifungal agents, plasticizers, and viscosity imparting agents. Examples thereof include additives, thermoplastic resins, and curable oligomers.

上記のようにして得られる架橋重合体の復元率は、通常80%以上である。   The restoration rate of the crosslinked polymer obtained as described above is usually 80% or more.

<実施例>
以下、実施例によって本発明を更に詳細に説明するが、本発明はこれら実施例のみに制限されるものではない。
なお、各物性の測定方法は下記のとおりである。
<Example>
EXAMPLES Hereinafter, although an Example demonstrates this invention further in detail, this invention is not restrict | limited only to these Examples.
In addition, the measuring method of each physical property is as follows.

1.破断強度、500%伸び時強度および破断伸度:JIS K7113に準じる。23℃で引張強度を測定し、60℃では溶融時でのゴム強度を測定する。
2.シートの均一性:目視評価による。
3.復元率:10cm×1cm×2mmの短冊状シートを80℃の湯浴に浸し、20cmまで伸張させ、一度冷却固化させる。再び80℃の湯浴に浸し、収縮させ、復元率を算出する。
4.シートの透明性:厚さ2mmのシートを目視評価した。○:完全に透明,△:若干白濁する,×:スリガラス状に白濁する。
1. Breaking strength, strength at 500% elongation and elongation at break: according to JIS K7113. The tensile strength is measured at 23 ° C., and the rubber strength at the time of melting is measured at 60 ° C.
2. Sheet uniformity: According to visual evaluation.
3. Restoration rate: A strip-shaped sheet of 10 cm × 1 cm × 2 mm is immersed in a hot water bath at 80 ° C., stretched to 20 cm, and once cooled and solidified. It is immersed again in a hot water bath at 80 ° C. and contracted, and the restoration rate is calculated.
4). Sheet transparency: A sheet having a thickness of 2 mm was visually evaluated. ○: completely transparent, Δ: slightly cloudy, ×: cloudy like ground glass.

[実施例1および2]
市場で入手したポリトランスイソプレン系樹脂シート(30cm×20cm×3mm)を、細かく切断した。このものを、プレス成形により20cm×20cm×2mmのシートに作製し直した。
[Examples 1 and 2]
A polytransisoprene resin sheet (30 cm × 20 cm × 3 mm) obtained on the market was finely cut. This was remade into a 20 cm × 20 cm × 2 mm sheet by press molding.

また、別にこの樹脂100重量部に対して、トリメチロールプロパンエチレンオキサイド付加トリアクリレート(ダイセル−UCB製TMPEOTA)を1重量部の割合で添加し、東洋精機製ラボプラストミルミキサーを用い120℃で2分間溶融混練した混合樹脂を用い、プレス成形により20cm×20cm×2mmのシートを作製した。   Separately, trimethylolpropane ethylene oxide-added triacrylate (Daicel-UCB TMPEOTA) was added at a ratio of 1 part by weight with respect to 100 parts by weight of the resin, and 2 ° C. at 120 ° C. using a Toyo Seiki Lab Plast Mill mixer. A 20 cm × 20 cm × 2 mm sheet was produced by press molding using a mixed resin melt-kneaded for a minute.

これらのシートに加速電圧200kV、吸収線量5Mradの条件でシートの両面に電子線(EB)照射を行った。これらのシートの23℃および60℃における引張試験を行い、さらに、シートの均一性、複元率を評価した。結果を表−1に示す。   These sheets were subjected to electron beam (EB) irradiation on both surfaces of the sheet under the conditions of an acceleration voltage of 200 kV and an absorbed dose of 5 Mrad. These sheets were subjected to a tensile test at 23 ° C. and 60 ° C., and the uniformity and the compound ratio of the sheets were evaluated. The results are shown in Table-1.

[比較例1]
比較のため、実施例1と同じポリトランスイソプレン系樹脂シート(20cm×20cm×2mm)の電子線(EB)照射をまったく実施しないものについて、実施例1と同様な評価を行った。結果を表−1に示す。
[Comparative Example 1]
For comparison, the same evaluation as in Example 1 was performed for the same polytransisoprene-based resin sheet (20 cm × 20 cm × 2 mm) that was not subjected to electron beam (EB) irradiation as in Example 1. The results are shown in Table-1.

[実施例3〜11および比較例2および3]
表−2に示した樹脂および多官能アクリル単量体としてトリス(アクリロキシエチル)イソシアヌレート(TAEIC)を用い、実施例1と同様にシートを作製した。得られたシートに加速電圧5,000kVの電子線照射を行った。比較例2および3は電子線照射をしなかった。得られたシートについてシートの均一性、シート透明性、復元率および75℃での500%伸び時の強度を測定し結果を表−2に示した。
[Examples 3 to 11 and Comparative Examples 2 and 3]
A sheet was prepared in the same manner as in Example 1 using tris (acryloxyethyl) isocyanurate (TAEIC) as the resin and the polyfunctional acrylic monomer shown in Table-2. The obtained sheet was irradiated with an electron beam at an acceleration voltage of 5,000 kV. Comparative Examples 2 and 3 were not irradiated with an electron beam. The obtained sheet was measured for sheet uniformity, sheet transparency, restoration rate, and strength at 500% elongation at 75 ° C., and the results are shown in Table 2.

Claims (5)

融点が40〜80℃であるポリトランスイソプレン系樹脂またはエチレン系共重合樹脂に活性エネルギー線を照射して架橋反応を起こすことにより得られることを特徴とする架橋重合体。   A crosslinked polymer obtained by irradiating an active energy ray to a polytransisoprene resin or ethylene copolymer resin having a melting point of 40 to 80 ° C. to cause a crosslinking reaction. ポリトランスイソプレン系樹脂またはエチレン系共重合樹脂がそれを構成する樹脂100重量部に対して多官能アクリル単量体または多官能アリル単量体を0.1〜30重量部混合した樹脂であることを特徴とする請求項1記載の架橋重合体。   The polytransisoprene resin or ethylene copolymer resin is a resin in which 0.1 to 30 parts by weight of a polyfunctional acrylic monomer or polyfunctional allyl monomer is mixed with 100 parts by weight of the resin constituting the polytransisoprene resin or ethylene copolymer resin. The crosslinked polymer according to claim 1. 請求項1または2に記載の架橋重合体から成ることを特徴とする放射線治療用シート。   A radiation treatment sheet comprising the crosslinked polymer according to claim 1. 請求項1または2に記載の架橋重合体から成ることを特徴とするギブス用シート。   A cast sheet comprising the crosslinked polymer according to claim 1 or 2. 請求項1または2に記載の架橋重合体から成ることを特徴とするかつらまたは歯の型取り用シート。   A wig or dental mold sheet comprising the crosslinked polymer according to claim 1 or 2.
JP2004204885A 1995-12-25 2004-07-12 Crosslinked polymer and medical sheet comprising the polymer Expired - Fee Related JP3714629B2 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1854439A1 (en) * 2006-05-08 2007-11-14 Orfit Industries Immobilisation device

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1854439A1 (en) * 2006-05-08 2007-11-14 Orfit Industries Immobilisation device
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