JPS62192440A - Shape memory molded body and its usage method - Google Patents
Shape memory molded body and its usage methodInfo
- Publication number
- JPS62192440A JPS62192440A JP3415086A JP3415086A JPS62192440A JP S62192440 A JPS62192440 A JP S62192440A JP 3415086 A JP3415086 A JP 3415086A JP 3415086 A JP3415086 A JP 3415086A JP S62192440 A JPS62192440 A JP S62192440A
- Authority
- JP
- Japan
- Prior art keywords
- shape
- melting point
- polymer
- molded body
- deformed
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 8
- 229920000642 polymer Polymers 0.000 claims description 38
- 150000001993 dienes Chemical class 0.000 claims description 22
- 238000002844 melting Methods 0.000 claims description 21
- 230000008018 melting Effects 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 14
- 238000010438 heat treatment Methods 0.000 claims description 11
- 229920003212 trans-1,4-polyisoprene Polymers 0.000 claims description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 229920001971 elastomer Polymers 0.000 description 12
- 239000005060 rubber Substances 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- 238000011084 recovery Methods 0.000 description 10
- 230000008961 swelling Effects 0.000 description 9
- 238000004132 cross linking Methods 0.000 description 8
- 239000003431 cross linking reagent Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 238000007906 compression Methods 0.000 description 7
- 230000006835 compression Effects 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000004073 vulcanization Methods 0.000 description 6
- 238000007654 immersion Methods 0.000 description 5
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 229920005549 butyl rubber Polymers 0.000 description 2
- 238000000748 compression moulding Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920001610 polycaprolactone Polymers 0.000 description 2
- 239000004632 polycaprolactone Substances 0.000 description 2
- 229920001195 polyisoprene Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000000899 Gutta-Percha Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 240000000342 Palaquium gutta Species 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000011952 anionic catalyst Substances 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 244000001591 balata Species 0.000 description 1
- 235000016302 balata Nutrition 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 229920003211 cis-1,4-polyisoprene Polymers 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000003484 crystal nucleating agent Substances 0.000 description 1
- 238000004455 differential thermal analysis Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 229920000588 gutta-percha Polymers 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000002648 laminated material Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Landscapes
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
(イ)産業上の利用分野
本発明は、融点40〜100℃の結晶性ジエン系重合体
を用いた形状記憶性を有する架橋成形体およびその使用
方法に関する。DETAILED DESCRIPTION OF THE INVENTION (a) Field of Industrial Application The present invention relates to a crosslinked molded article having shape memory properties using a crystalline diene polymer having a melting point of 40 to 100° C., and a method for using the same.
(ロ) 従来の技術
高分子化合物の成形体において、その形状のままでは装
着や組立て、搬送等の作業が困難な場合に、変形を与え
て作業の際の取扱いが容易となる様に形状を変え、装着
や組立て等が終了した後で加熱操作等によシ所定の形状
に回復させ、本来の目的とする働きをさせることまたは
変形した成形体を元の状態に回復させること自体に主点
を置いた用途等に適した材料、すなわち形状記憶性成形
体について従来から種々検討がなされている。(b) Conventional technology When it is difficult to attach, assemble, or transport a molded article of a polymer compound in its original shape, it is possible to deform it so that it can be easily handled during work. The main point is to restore the predetermined shape by heating operation etc. after the modification, installation, assembly, etc., and to make it work as intended, or to restore the deformed molded product to its original state. In the past, various studies have been conducted on materials suitable for applications such as shape-memory molded bodies.
従来から、形状記憶性成形体については例えば、ノルボ
ルネン系ポリマー成形体(%開昭59−53528号公
報参照)、共役ジエンまたはエポキシ基含有等と芳香族
ビニル、不飽和ニトリルまたはアクリル酸エステル等と
の共1合体成形体(%開昭60−28433号公報参照
)らるいはポリカプロラクトンを用いた架橋成形体(特
開昭59−11315号参照)等知られているが、それ
らは加工性が良くない、または形状を回復させる温度が
高い等、何れも一長一短がらった。Conventionally, shape-memory molded products have been produced, for example, norbornene-based polymer molded products (see Japanese Patent Publication No. 59-53528), conjugated diene or epoxy group-containing materials, and aromatic vinyl, unsaturated nitrile or acrylic esters. Polycaprolactone is known as a cross-linked molded product (see JP-A-60-28433) or a cross-linked molded product using polycaprolactone (see JP-A-59-11315). All of them had their pros and cons, such as not being good or requiring high temperatures to recover the shape.
(ハ) 発明が解決しようとする問題点本発明等は、成
形加工性にすぐれ、そのままの形状では袋着、組立て、
搬送等の作業の困難な場合に作業しやすい形状に一旦変
形し、前記作業を行なった後に加熱操作により当初の所
定の形状に回復させ、前記作業を終了させるというやり
方で用いるのに適した形状記憶性成形体または変形した
成形体を元の状態に回復させること自体を目的とする形
状記憶性成形体およびその使用方法を提供することを目
的とし、鋭意検討を重ねた結果、本発明を完成するに至
つ九。(c) Problems to be Solved by the Invention The present invention has excellent moldability, and in its original form it is difficult to bag, assemble, and
A shape suitable for use in cases where work such as transportation is difficult, by temporarily deforming into a shape that is easy to work with, and then restoring it to the original predetermined shape by heating operation after performing the work to complete the work. The present invention was completed as a result of extensive research aimed at providing a shape-memory molded article and a method for using the same, the purpose of which is to restore a memorized molded article or a deformed molded article to its original state. 9.
に)問題点を解決するための手段
本発明によれば、上記目的は、融点40〜100℃の結
晶性ジエン系重合体を主成分とする組成物からの架橋成
形体でるり、所望の形状に変形でき、かつ前記重合体の
融点以下の温度で、該変形が固定できることを特徴とす
る形状記憶性成形体によって、また融点40〜100℃
の結晶性ジエン系重合体を主成分とする組成物からの架
橋成形体を所望の形状に変形し、次いで前記重合体の融
点以下の温度に冷却して変形を固定した形状記憶性架橋
成形体を前記重合体の融点以上の温度に加熱して該成形
体の当初の形状を回復させることからなる使用方法によ
って達成される。B.) Means for Solving the Problems According to the present invention, the above object is to produce a crosslinked molded product from a composition containing a crystalline diene polymer having a melting point of 40 to 100°C as a main component, and to obtain a desired shape. A shape-memory molded article having a melting point of 40 to 100° C. can be deformed to a temperature of 40 to 100° C., and the deformation can be fixed at a temperature below the melting point of the polymer.
A shape-memory crosslinked molded product obtained by deforming a crosslinked molded product made from a composition containing a crystalline diene polymer as a main component into a desired shape, and then cooling the deformation to a temperature below the melting point of the polymer to fix the deformation. This is achieved by a method of use comprising heating the molded article to a temperature above the melting point of the polymer to restore the original shape of the molded article.
前記成形体は、一旦実際の使用に必要な形状に架橋成形
した後特定の温度下にて変形を与えても、再度特定の温
度に加熱することにより変形は自動的に除去され成形体
当初の形状またはそれに近い形状に回復させることがで
きることから、このような機能が要求される分野での種
々の利用が可能である。Even if the molded body is deformed at a certain temperature after being cross-linked into the shape required for actual use, the deformation is automatically removed by heating it again to the specified temperature, and the molded body returns to its original state. Since it can be restored to the shape or a shape close to it, it can be used in various fields where such functions are required.
本発明においては融点40〜100℃の結晶性ジエン系
重合体を主成分とする組成物を用いるが、本発明は該重
合体が常温(25℃)ですぐれた強度と弾性を有し、比
較的低温で成形できるという特性を利用してなされたも
のでめる。なお5本発明において融点とは示差熱分析に
よって測定される重合体の結晶の融解による吸熱ピーク
の最も高温側の吸熱ピークを意味する。In the present invention, a composition mainly composed of a crystalline diene polymer with a melting point of 40 to 100°C is used. It is made by taking advantage of the property that it can be molded at a relatively low temperature. 5 In the present invention, the melting point refers to the endothermic peak on the highest temperature side of the endothermic peaks due to melting of crystals of the polymer measured by differential thermal analysis.
このような条件を満たす重合体としては、ブタジェン、
イソグレンまたはクロロプレン等の共役ジエンからなる
結晶性重合体でおればよく、最も好ましい例としては、
トランス−1,4−ポリインプレンまたはシンジオタク
チック−1,2−ポリブタジェンが挙げられる。とりわ
け、トランス−1゜4−ポリインプレンが最適でるる。Polymers that meet these conditions include butadiene,
Any crystalline polymer consisting of a conjugated diene such as isogrene or chloroprene may be used, and the most preferred example is:
Trans-1,4-polyimprene or syndiotactic-1,2-polybutadiene may be mentioned. In particular, trans-1°4-polyinprene is most suitable.
これらの結晶性重合体の結晶化度が低いと、該重合体を
主成分とする組成物から得られる架橋成形体の強度が不
充分となるので、前記重合体は高い立体規則性を示す構
造をとる必要があり、例えばトランス−1゜4−ポリイ
ンプレンの場合には90%以上、好ましくは95%以上
のトランス−1,4M合を含有することが望ましく、ま
たシンジオタクチック−1,2−ポリブタジェンの場合
には90%以上、好ましくは95%以上の1,2−結合
を有することが望ましいO
また、前記結晶性ジエン系重合体の分子量が小さ過ざる
と、その強度が低下し、一方分子量が大き過ぎると溶融
粘度が大きくなり、成形加工性が低下するので本発明で
使用する結晶性ジエン系重合体は30℃のトルエン中に
おける極限粘度が1.2〜4.5、好ましくは1.5〜
3.5の範囲内にめるのが望ましい。If the crystallinity of these crystalline polymers is low, the strength of the crosslinked molded product obtained from the composition containing the polymer as a main component will be insufficient, so the polymer has a structure that exhibits high stereoregularity. For example, in the case of trans-1゜4-polyimprene, it is desirable to contain trans-1,4M of 90% or more, preferably 95% or more. In the case of 2-polybutadiene, it is desirable to have 90% or more, preferably 95% or more of 1,2-bonds.In addition, if the molecular weight of the crystalline diene polymer is too small, its strength will decrease. On the other hand, if the molecular weight is too large, the melt viscosity will increase and the molding processability will decrease. Therefore, the crystalline diene polymer used in the present invention has an intrinsic viscosity of 1.2 to 4.5 in toluene at 30°C, preferably is 1.5 ~
It is desirable to keep it within the range of 3.5.
このような結晶性重合体としては、バラタもしくはガツ
タパーチャ等の天然トランス−1,4−ポリイソプレン
、または合成トランス−1,4−ポリイソプレンが挙げ
られる。本発明で好ましく用いられる合成トランス−1
,4−ポリインプレンの場合にはイソプレン単量体をチ
ーグラー系触媒を用いて重合することによって、ま念シ
ンジオタクチックー1,2−ポリブタジェンの場合には
ブタジェン単量体をアニオン型触媒を用いて重合するこ
とによって得られる。Such crystalline polymers include natural trans-1,4-polyisoprene, such as balata or gutta-percha, or synthetic trans-1,4-polyisoprene. Synthetic trans-1 preferably used in the present invention
In the case of ,4-polyimprene, isoprene monomer is polymerized using a Ziegler catalyst, and in the case of syndiotactic-1,2-polybutadiene, butadiene monomer is polymerized using an anionic catalyst. It can be obtained by polymerization using
本発明において架橋成形体音つくるために組成物は、融
点40〜100℃の結晶性ジエン系重合体を主成分とし
、架橋剤を含有するものでちるが、組成物の融点が40
〜110℃、好ましくは50〜100℃の範囲内にあっ
て、加工性や強度を損わず、しかも、架橋成形体にした
ときに変形を与えた際に亀裂音生じさせない範囲で、具
体的には結晶性ジエン系重合体1003!量部に対して
40重量部以下の範囲で、天然ゴム、合成シス−1,4
−ポリイソプレンゴム(IR)、ポリブタジェンゴム(
BR)、スチレン−ブタジェン共i 合体=’ム(SB
R)、スチレン−インプレン共重合体ゴム(SIR)、
アクリロニトリル−ブタジェン共重合体ゴム(NBR)
、アクリロニトリル−イソプレン共重合体ゴム(NIR
)、エチレン−プロピレン共重合ゴム(EPRlたはE
PDM)またはブチルゴム(IIR)等のゴム、まえは
それらの混合物を配合してもよい。あるいは、さらに必
要に応じて充填剤、ゴム補強剤、ゴム軟化剤、可辺剤、
結晶核剤、老化防止剤、酸化防止剤、オゾン劣化防止剤
、紫外線吸収剤、顔料、染料または粘着付与樹脂等のゴ
ム、プラスチック配合剤を配合してもよい。In the present invention, in order to create the sound of a crosslinked molded product, the composition is mainly composed of a crystalline diene polymer having a melting point of 40 to 100°C and contains a crosslinking agent.
-110°C, preferably 50-100°C, within a range that does not impair workability or strength, and does not cause cracking noise when deformed when made into a crosslinked molded product. Crystalline diene polymer 1003! Natural rubber, synthetic cis-1,4 within a range of 40 parts by weight or less
-Polyisoprene rubber (IR), polybutadiene rubber (
BR), styrene-butadiene combination='mu(SB
R), styrene-imprene copolymer rubber (SIR),
Acrylonitrile-butadiene copolymer rubber (NBR)
, acrylonitrile-isoprene copolymer rubber (NIR
), ethylene-propylene copolymer rubber (EPRl or E
Rubbers such as PDM) or butyl rubber (IIR) or mixtures thereof may also be incorporated. Alternatively, if necessary, fillers, rubber reinforcing agents, rubber softeners, abposable agents, etc.
Rubber and plastic compounding agents such as crystal nucleating agents, anti-aging agents, antioxidants, anti-ozonants, ultraviolet absorbers, pigments, dyes, or tackifying resins may be added.
本発明において、融点40〜100℃の結晶性ジエン系
重合体を主成分とする架橋成形体のための組成物には架
橋剤が配合嘔れる。前記架橋剤としては、例えば通常ゴ
ム、プラスチック工業で一般に用いられている加硫剤が
用いられる。好ましい加硫剤の例としては硫黄および硫
黄供与性有機化合物、ジクミルパーオキサイド等の有機
過酸化物が挙げられる。架橋剤を配合する際には加硫促
進剤、加硫助剤または活性剤等の加硫薬品を用いてもよ
い。In the present invention, a crosslinking agent is blended into a composition for a crosslinked molded article which is mainly composed of a crystalline diene polymer having a melting point of 40 to 100°C. As the crosslinking agent, for example, a vulcanizing agent commonly used in the rubber and plastic industries is used. Examples of preferred vulcanizing agents include sulfur and sulfur-donating organic compounds, and organic peroxides such as dicumyl peroxide. When blending the crosslinking agent, vulcanization chemicals such as vulcanization accelerators, vulcanization aids, or activators may be used.
架橋剤の使用量は、一般に通常のゴム工業における使用
範囲にあるが、結晶性ジエン系重合体、架橋剤の種類、
他の配合剤の量等によって異なり、形状記憶性との関係
から一概に決められるものではなく、架橋剤の使用量は
、形状記憶性との関係から架橋成形体の架橋密度の関係
で規定した方が好ましい。架橋成形体が形状記憶性を示
し、該成形体を所望の形に変形する際に、または変形さ
せた成形体を元の形に戻す際に成形体に亀裂発生等の不
都合を生じないようにするためには、架橋剤は架橋密度
が2.5 X 10−’モル/を以下、好ましくは0、
lX10 〜2.5X10 モル/’s特に好ましく
は0.3 X 10−’〜2.2 X 10−’モル/
fの範囲内となる量を用いるのが望ましい。架橋密度が
小さ過ぎると賦をした架橋成形体を一旦変形した後加熱
しても当初の形に回復しない。架橋密度が適切な範囲に
わると、好ましい場合には変形除去後当初の状態の60
%以上、特に好ましい場合には95チ以上回復する。一
方、架橋密度が大き過ぎると架橋成形体を賦型したとき
にまたは当初の形に戻すときに亀裂を生じるようになる
。The amount of crosslinking agent used is generally within the range used in the normal rubber industry, but it depends on the crystalline diene polymer, the type of crosslinking agent,
It varies depending on the amount of other compounding agents, etc., and cannot be determined unconditionally from the relationship with shape memory.The amount of crosslinking agent used is determined from the relationship with shape memory and the crosslink density of the crosslinked molded product. is preferable. The crosslinked molded product exhibits shape memory properties so that inconveniences such as cracking in the molded product do not occur when the molded product is deformed into a desired shape or when the deformed molded product is returned to its original shape. In order to
lX10 to 2.5X10 mol/'s, particularly preferably 0.3 X 10-' to 2.2 X 10-'mol/'
It is desirable to use an amount within the range of f. If the crosslinking density is too low, the applied crosslinked molded product will not recover to its original shape even if it is heated after being deformed. When the crosslinking density falls within a suitable range, it is preferable that 60% of the original state after deformation is removed.
% or more, particularly preferably 95% or more. On the other hand, if the crosslinking density is too high, cracks will occur when the crosslinked molded product is shaped or returned to its original shape.
ここで架橋成形体の架橋密度(ν)は膨潤度qを求め、
膨潤度より膨潤試料中の結晶性ジエン系重合体の容積分
率(v2)を求め、該分率(v2)からフロリー・ブー
チェの式(P、 J、 Flory、 A、M、 Bu
s che)により算出されるものでめる。膨潤度(Q
は架橋成形体を浸漬液(ベンゼン使用)に浸漬し、膨潤
前後の1量を測定し、それをもとに次式により算出され
る。Here, the crosslink density (ν) of the crosslinked molded body is determined by the degree of swelling q,
The volume fraction (v2) of the crystalline diene polymer in the swollen sample is determined from the degree of swelling, and the Flory-Boucher equation (P, J, Flory, A, M, Bu
s che). Degree of swelling (Q
The crosslinked molded body is immersed in an immersion liquid (using benzene), the amount before and after swelling is measured, and the amount is calculated from the following formula based on the measurement.
式中、Wb:膨潤後の架橋成形体の重量Wa:膨潤前の
架橋成形体のJa量
ρl:結晶性ジエン系重合体の密度(r//?II)ρ
2:浸漬液の密度(な−)
γ;配合による補正項
膨潤試料中の重合体の容積分率(v2)は次式により算
出される。In the formula, Wb: weight of the crosslinked molded product after swelling Wa: amount of Ja of the crosslinked molded product before swelling ρl: density of the crystalline diene polymer (r//?II) ρ
2: Density of the immersion liquid (na-) γ: Correction factor due to formulation The volume fraction (v2) of the polymer in the swollen sample is calculated by the following formula.
また、フロリーブ−チェの式は次式で表わされる。Further, the Floriebouche equation is expressed by the following equation.
シ工l /Mc
カニ単量重量あたりの架橋の数(mol/f)MC:架
橋間の鎖の平均分子量
μ:重合体の相互溶解度係数
■1:1:浸漬液ル容積(cc/mol)M:架橋前の
重合体の平均分子量
架橋成形体の製造は、結晶性ジエン系重合体および架橋
剤、さらにはそれらに必要に応じてゴム、プラスチック
配合剤を例えばオープンロール、バンバリーミキサ−ま
たはニーダ−等により混合して架橋性組成物を調製し、
次いで該組成物を例えば押出成形、射出成形、圧縮成形
等で所望の形に成形し、次いで架橋することによって行
われる。/Mc Number of crosslinks per unit weight of crab (mol/f) MC: Average molecular weight of chains between crosslinks μ: Mutual solubility coefficient of polymer ■1:1: Volume of immersion liquid (cc/mol) M: Average molecular weight of polymer before crosslinking Production of a crosslinked molded product involves adding a crystalline diene polymer, a crosslinking agent, and rubber and plastic compounding agents to them as necessary, for example, using an open roll, a Banbury mixer, or a kneader. - etc. to prepare a crosslinkable composition,
The composition is then molded into a desired shape by, for example, extrusion molding, injection molding, compression molding, etc., and then crosslinked.
前記組成物は加熱等の架橋化処理前には結晶性ジエン系
重合体の融点をこえる温度で成形加工できるものである
。成形条件および架橋条件は所望の形で架橋密度が前述
した範囲内にあれば特に限定されるものではない。The composition can be molded at a temperature exceeding the melting point of the crystalline diene polymer before crosslinking treatment such as heating. The molding conditions and crosslinking conditions are not particularly limited as long as the desired shape and crosslinking density are within the above-mentioned range.
このようにして所望の形とされた架橋成形体は、該成形
体の形状または肉厚に応じて素手、工具らるいは成縮成
形機等の装置を用いて所望とする第2の形に変形されて
用いられる。変形させる際の温度は該成形体が容易に変
形し、かつ変形時に亀裂を生じさせない温度でろればよ
い。一般的には結晶性ジエン系重合体の融点以上の温度
が好ましい。変形温度が前記融点以上である場合には変
形後前記融点以下に急冷し、変形を固定することが好ま
しい。The crosslinked molded product thus formed into the desired shape is shaped into the desired second shape using bare hands, a tool, or a device such as a compression molding machine, depending on the shape or wall thickness of the molded product. Used in modified form. The temperature at which the molded body is deformed may be a temperature that allows the molded body to be easily deformed and does not cause cracks during deformation. Generally, the temperature is preferably higher than the melting point of the crystalline diene polymer. When the deformation temperature is above the melting point, it is preferable to rapidly cool the material after deformation to below the melting point to fix the deformation.
このようにして得られた形状記憶成形体を当初の形状に
おるいはそれに近い形状に戻すには結晶性ジエン系重合
体の融点以上に加熱すればよく、それによって変形は自
動的に除去され、形状が回復する。上記の加熱に際して
は60〜100℃の温水、100℃前後の熱風が好まし
く用いられる。In order to return the shape memory molded body obtained in this way to its original shape or a shape close to it, it is sufficient to heat it above the melting point of the crystalline diene polymer, and the deformation is thereby automatically removed. , the shape is restored. In the above heating, hot water at 60 to 100°C and hot air at around 100°C are preferably used.
なお、成形体を60〜100℃の温度にしても成形体は
熱伝導度が低いので、人肌に接触させても火傷の心配が
なく、この点にも本発明の形状記憶性成形体のメリット
がある。In addition, even if the molded product is heated to a temperature of 60 to 100°C, the molded product has low thermal conductivity, so there is no risk of burns even if it comes into contact with human skin, and this is also an advantage of the shape memory molded product of the present invention. There are benefits.
本発明の形状記憶性成形体は、一旦変形させた成形体を
所定の形状まで回復しうるので、成形体の使用の際に、
その形状のままでは装着や組立て、搬送等が困難な場合
に取扱いが容易になる梯形状を変え、装着や組立て等が
終了した後で加熱操作により所定の形状に回復させ、本
来の目的とする働きをさせるのに、また変形した成形体
を元の状態に回復させること自体に主点を置いた用途に
使用できる。具体的には前者では、パイプや電線等の接
合部の接合材やシール材、パイプや棒状物体の内、外部
ラミネート材、スプリント材、各種固定材、衝隼吸収材
等、後者では、玩具用部材、文具材、教材、装飾品材等
である。The shape-memory molded article of the present invention can recover a once-deformed molded article to a predetermined shape, so when using the molded article,
When mounting, assembling, transporting, etc. is difficult in that shape, the ladder shape is changed to make it easier to handle, and after the mounting, assembly, etc. are completed, it is restored to the specified shape by heating operation, and the original purpose is achieved. It can be used for purposes that focus on restoring a deformed molded body to its original state. Specifically, the former includes bonding materials and sealing materials for joints of pipes and electric wires, external laminate materials for pipes and rod-shaped objects, splint materials, various fixing materials, impact absorbing materials, etc., and the latter includes materials for toys. These include parts, stationery materials, teaching materials, decorative materials, etc.
(ホ)実施例および効果
以下、実施例により本発明を具体的に説明するが、本発
明はこれらの実施例に限定されるものではない。なお、
実施例中における「部」は、特に断わらない限り「重仕
部」を意味する。(E) Examples and Effects The present invention will be specifically explained below with reference to Examples, but the present invention is not limited to these Examples. In addition,
In the examples, "part" means "heavy section" unless otherwise specified.
実施例1
30℃のトルエン中で測定した極限粘度3,2、トラン
ス−1,4結合金有ff199%のトランス−1゜4−
ポリイソプレン〔クラレインプレンケミカル■裂、クラ
レトランスボリイソプレンTP−301)100部、軽
質炭酸カルシウム30部、硫黄0.5部、ジクミルパー
オキサイド〔日本油脂■製、)く−クミルD)3部を8
インチオープンロールを用いて、75部5℃で混線し、
シートを作成した。Example 1 Intrinsic viscosity measured in toluene at 30°C, 3,2, 199% trans-1°4- with trans-1,4 alloy
100 parts of polyisoprene [Kurarein Prene Chemical ■, Kuraray Transbolyisoprene TP-301], 30 parts of light calcium carbonate, 0.5 parts of sulfur, dicumyl peroxide [manufactured by Nippon Oil & Fats Corporation, ) Ku-cumyl D) 3 Part 8
Using an inch open roll, mix 75 parts at 5℃,
I created a sheet.
このシートを圧縮永久歪用金型を用い、100℃で5分
間予熱後、100℃で5分間、60KQ/crAの圧力
で圧縮成形し、次いで145℃で30分間加硫を行ない
、架橋成形体サンプルを得之。次にこの成形体(5)を
、80℃10分子熱後4鴎金枠を用いて、100℃5分
、60Kf/−の圧力で圧縮し、変形を与えた後、室温
迄冷却し変形固定した。この変形した成形体(B)を7
0℃温水に10分間浸漬し九ところ、成形体が元の状態
に回復し、形状記憶性成形体が得られたことが判った。This sheet was preheated at 100°C for 5 minutes using a compression set mold, compression molded at 100°C for 5 minutes at a pressure of 60 KQ/crA, and then vulcanized at 145°C for 30 minutes, resulting in a crosslinked molded product. Obtain a sample. Next, this molded body (5) was heated at 80°C for 10 molecules, and then compressed using a 4-magnet frame at 100°C for 5 minutes at a pressure of 60Kf/- to give it deformation, and then cooled to room temperature to fix the deformation. did. This deformed molded body (B)
After immersion in 0°C hot water for 10 minutes, the molded body recovered to its original state, indicating that a shape-memory molded body had been obtained.
成形体の圧縮変形し、次いで加熱回復した状況を第1図
に示す。形状記憶性の指標として次式で求められる変形
回復率(%)を求めたところ、直径口および高さのでの
変形回復率は各々100%でめった。FIG. 1 shows the state in which the compact was compressively deformed and then recovered by heating. When the deformation recovery rate (%) determined by the following formula was determined as an index of shape memory property, the deformation recovery rate at the diameter opening and height were each 100%.
変形回復率(%)
DO=圧縮変形前のサンプルの直径
D1:圧縮変形したサンプルの直径
D2:加熱回復したサンプルの直径
TO:圧縮変形前のサンプルの高き
T1:圧縮変形したサンプルの高さ
T2:圧縮回復したサンプルの高さ
1だ架橋成形体(5)の架橋密度をみるために次の条件
でベンゼン溶解度およびベンゼン膨潤度を調べたところ
、前者は247%、後者は5.0%でめった。Deformation recovery rate (%) DO = Diameter of the sample before compression deformation D1: Diameter of the sample after compression deformation D2: Diameter of the sample after heating recovery TO: Height of the sample before compression deformation T1: Height of the sample after compression deformation T2 :The height of the compressed sample was 1. In order to check the crosslinking density of the crosslinked molded body (5), the benzene solubility and benzene swelling degree were investigated under the following conditions, and the former was 247% and the latter was 5.0%. Rarely.
・サンプルのベンゼン浸漬条件
80℃、60分間
・ベンゼン溶解度
Wa −Wc
溶解度= wa ×100
・ベンゼン膨潤度
Wb −We
膨潤度(1%)= wo ×100
実施例2
軽質炭酸カルシウムの使用量を150部とすること以外
は実施例1と同様の方法で架橋成形体を作製した。実施
例1と同様の方法により変形回復率を調べたところ、第
1表に示した結果が得られた。・Sample immersion conditions in benzene at 80°C for 60 minutes ・Benzene solubility Wa - Wc Solubility = wa × 100 ・Benzene swelling degree Wb - We Swelling degree (1%) = wo × 100 Example 2 The amount of light calcium carbonate used was 150 A cross-linked molded body was produced in the same manner as in Example 1 except that When the deformation recovery rate was investigated using the same method as in Example 1, the results shown in Table 1 were obtained.
実施例3
軽質炭酸カルシウムの使用量を150部とし、ナフテン
系プロセスオイルを30部添加し、加硫時間を40分と
すること以外は実施例1と同様の方法で架橋成形体を作
製した。その変形回復率を第1表に示した。Example 3 A crosslinked molded body was produced in the same manner as in Example 1, except that the amount of light calcium carbonate used was 150 parts, the naphthenic process oil was added 30 parts, and the vulcanization time was 40 minutes. The deformation recovery rate is shown in Table 1.
実施例4
トランス−1,4−ポリイソプレンの使用tit’t7
0部とし、シス−1,4−ポリインプレン全30部添加
すること以外は実施例1と同様の方法により架橋成形体
を作製した。その変形回復率を第1表に示した。Example 4 Use of trans-1,4-polyisoprene tit't7
A crosslinked molded body was produced in the same manner as in Example 1 except that 30 parts of cis-1,4-polyinprene was added. The deformation recovery rate is shown in Table 1.
実施例5
ジクミルパーオキサイドを全く使用せず、加硫促進剤を
3部添加し、加硫時間を25分とする以外は実施例1と
同様の方法により架橋成形体全作製した。その変形回復
率を第1表に示した。Example 5 A crosslinked molded article was entirely prepared in the same manner as in Example 1, except that dicumyl peroxide was not used at all, 3 parts of a vulcanization accelerator was added, and the vulcanization time was 25 minutes. The deformation recovery rate is shown in Table 1.
比較例1および2
硫黄およびジクミルパーオキサイドを全く使用しないこ
と以外は実施例1と同様の方法により成形体を作製した
。また、この方法においてトランス−1,4ポリインプ
レンの使用量を70部とし、シス−1,4−ポリイソプ
レンを30部添加すること以外は前記と同様の方法によ
り成形体を作製した○
このようにしてイυられた成形体について変形回復率を
調べた。その結果を第1表に示した。Comparative Examples 1 and 2 Molded bodies were produced in the same manner as in Example 1 except that sulfur and dicumyl peroxide were not used at all. In addition, in this method, a molded body was produced in the same manner as above except that the amount of trans-1,4 polyimprene used was 70 parts and cis-1,4-polyisoprene was added 30 parts. The deformation recovery rate of the molded bodies thus prepared was investigated. The results are shown in Table 1.
第1図は、本発明の形状記憶成形体を圧縮変形−加熱回
復したときの形状の変化を示した1例でろる。図中、A
は形状記憶成形体、Bは該成形体を圧縮変形したもの、
Cは変形したものを加熱回復したものでろる。FIG. 1 is an example showing the change in shape when the shape memory molded article of the present invention is subjected to compression deformation and heating recovery. In the figure, A
is a shape memory molded body, B is a compressed and deformed molded body,
C is a deformed material that has been heated and recovered.
Claims (4)
成分とする組成物からの架橋成形体であって、所望の形
状に変形でき、かつ前記重合体の融点以下の温度で該変
形が固定できることを特徴とする形状記憶性成形体。(1) A crosslinked molded article made from a composition mainly composed of a crystalline diene polymer with a melting point of 40 to 100°C, which can be deformed into a desired shape and can be deformed at a temperature below the melting point of the polymer. A shape-memory molded body characterized by being able to be fixed.
イソプレンである特許請求の範囲第1項記載の成形体。(2) The molded article according to claim 1, wherein the crystalline diene polymer is trans-1,4-polyisoprene.
成分とする組成物からの架橋成形体を所望の形状に変形
し、次いで前記重合体の融点以下の温度に冷却して変形
を固定した形状記憶性架橋成形体を前記重合体の融点以
上の温度に加熱して該成形体の当初の形状に回復させる
ことを特徴とする形状記憶性成形体の使用方法。(3) A crosslinked molded product made from a composition mainly composed of a crystalline diene polymer with a melting point of 40 to 100°C is deformed into a desired shape, and then cooled to a temperature below the melting point of the polymer to remove the deformation. A method for using a shape-memory molded article, which comprises heating the fixed shape-memory crosslinked molded article to a temperature equal to or higher than the melting point of the polymer to recover the original shape of the molded article.
イソプレンである特許請求の範囲第3項記載の使用方法
。(4) The method of use according to claim 3, wherein the crystalline diene polymer is trans-1,4-polyisoprene.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3415086A JPS62192440A (en) | 1986-02-18 | 1986-02-18 | Shape memory molded body and its usage method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3415086A JPS62192440A (en) | 1986-02-18 | 1986-02-18 | Shape memory molded body and its usage method |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62192440A true JPS62192440A (en) | 1987-08-24 |
Family
ID=12406167
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3415086A Pending JPS62192440A (en) | 1986-02-18 | 1986-02-18 | Shape memory molded body and its usage method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62192440A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6485303A (en) * | 1987-09-28 | 1989-03-30 | Aderans Kk | Wig having shape holding member |
JPH0257323A (en) * | 1988-08-22 | 1990-02-27 | Osaka Gas Co Ltd | Lining method for inner face of tube |
JPH02118701U (en) * | 1989-03-10 | 1990-09-25 | ||
JPH08199080A (en) * | 1995-01-26 | 1996-08-06 | Mitsubishi Cable Ind Ltd | Shape-memory composite |
US7723460B2 (en) | 2003-12-12 | 2010-05-25 | Nec Corporation | Shape-memory resin performing remoldability and excellent in shape recovering property, and molded product composed of the cross-linked resin |
WO2010107527A2 (en) | 2009-03-14 | 2010-09-23 | Raytheon Company | Method of manufacture of one-piece composite parts |
WO2011003832A1 (en) * | 2009-07-06 | 2011-01-13 | Technische Universität Dortmund | Polymer or polymer network |
WO2015045940A1 (en) * | 2013-09-30 | 2015-04-02 | 日立造船株式会社 | Shape memory resin composition |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57185367A (en) * | 1981-05-11 | 1982-11-15 | Kuraray Co Ltd | Adhesive composition |
JPS61231051A (en) * | 1985-04-06 | 1986-10-15 | Sumitomo Electric Ind Ltd | Shape memory article |
-
1986
- 1986-02-18 JP JP3415086A patent/JPS62192440A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57185367A (en) * | 1981-05-11 | 1982-11-15 | Kuraray Co Ltd | Adhesive composition |
JPS61231051A (en) * | 1985-04-06 | 1986-10-15 | Sumitomo Electric Ind Ltd | Shape memory article |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6485303A (en) * | 1987-09-28 | 1989-03-30 | Aderans Kk | Wig having shape holding member |
JPH0257323A (en) * | 1988-08-22 | 1990-02-27 | Osaka Gas Co Ltd | Lining method for inner face of tube |
JPH02118701U (en) * | 1989-03-10 | 1990-09-25 | ||
JPH08199080A (en) * | 1995-01-26 | 1996-08-06 | Mitsubishi Cable Ind Ltd | Shape-memory composite |
US7723460B2 (en) | 2003-12-12 | 2010-05-25 | Nec Corporation | Shape-memory resin performing remoldability and excellent in shape recovering property, and molded product composed of the cross-linked resin |
WO2010107527A2 (en) | 2009-03-14 | 2010-09-23 | Raytheon Company | Method of manufacture of one-piece composite parts |
WO2011003832A1 (en) * | 2009-07-06 | 2011-01-13 | Technische Universität Dortmund | Polymer or polymer network |
WO2015045940A1 (en) * | 2013-09-30 | 2015-04-02 | 日立造船株式会社 | Shape memory resin composition |
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