JPH05247413A - Sealing member - Google Patents
Sealing memberInfo
- Publication number
- JPH05247413A JPH05247413A JP4084794A JP8479492A JPH05247413A JP H05247413 A JPH05247413 A JP H05247413A JP 4084794 A JP4084794 A JP 4084794A JP 8479492 A JP8479492 A JP 8479492A JP H05247413 A JPH05247413 A JP H05247413A
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- foaming agent
- adhesive layer
- case
- group
- 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.)
- Granted
Links
- 238000007789 sealing Methods 0.000 title claims abstract description 14
- 239000000853 adhesive Substances 0.000 claims abstract description 44
- 230000001070 adhesive effect Effects 0.000 claims abstract description 44
- 239000012790 adhesive layer Substances 0.000 claims abstract description 25
- 239000004088 foaming agent Substances 0.000 claims abstract description 20
- 239000010410 layer Substances 0.000 claims abstract description 9
- 239000000758 substrate Substances 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 abstract description 11
- 239000000463 material Substances 0.000 abstract description 6
- 230000007423 decrease Effects 0.000 abstract description 3
- 239000000565 sealant Substances 0.000 abstract 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 14
- 239000000123 paper Substances 0.000 description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000010419 fine particle Substances 0.000 description 6
- -1 2-ethylhexyl group Chemical group 0.000 description 5
- 229920005601 base polymer Polymers 0.000 description 5
- 239000006260 foam Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000005187 foaming Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 239000005060 rubber Substances 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000001099 ammonium carbonate Substances 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000004005 microsphere Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 238000011946 reduction process Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- XXANGWUMCMNLJD-UHFFFAOYSA-N 1-(benzenesulfonamido)-3-(benzenesulfonamidocarbamoylamino)oxyurea Chemical compound C=1C=CC=CC=1S(=O)(=O)NNC(=O)NONC(=O)NNS(=O)(=O)C1=CC=CC=C1 XXANGWUMCMNLJD-UHFFFAOYSA-N 0.000 description 1
- CQSQUYVFNGIECQ-UHFFFAOYSA-N 1-n,4-n-dimethyl-1-n,4-n-dinitrosobenzene-1,4-dicarboxamide Chemical compound O=NN(C)C(=O)C1=CC=C(C(=O)N(C)N=O)C=C1 CQSQUYVFNGIECQ-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- BLJHFERYMGMXSC-UHFFFAOYSA-N 3-[3-(hydrazinesulfonyl)phenyl]sulfonylbenzenesulfonohydrazide Chemical compound NNS(=O)(=O)C1=CC=CC(S(=O)(=O)C=2C=C(C=CC=2)S(=O)(=O)NN)=C1 BLJHFERYMGMXSC-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- GRRGMQBIAJCOBQ-UHFFFAOYSA-N 4-(thiatriazol-5-yl)morpholine Chemical compound C1COCCN1C1=NN=NS1 GRRGMQBIAJCOBQ-UHFFFAOYSA-N 0.000 description 1
- NBOCQTNZUPTTEI-UHFFFAOYSA-N 4-[4-(hydrazinesulfonyl)phenoxy]benzenesulfonohydrazide Chemical compound C1=CC(S(=O)(=O)NN)=CC=C1OC1=CC=C(S(=O)(=O)NN)C=C1 NBOCQTNZUPTTEI-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- 150000004008 N-nitroso compounds Chemical class 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- CAMXVZOXBADHNJ-UHFFFAOYSA-N ammonium nitrite Chemical compound [NH4+].[O-]N=O CAMXVZOXBADHNJ-UHFFFAOYSA-N 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
- 229940099364 dichlorofluoromethane Drugs 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 description 1
- 150000003349 semicarbazides Chemical class 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Adhesives Or Adhesive Processes (AREA)
- Sealing Material Composition (AREA)
- Adhesive Tapes (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、発泡剤を含有して加熱
処理で接着力が低減し、紙製ケース等よりそれを損傷さ
せずに剥離できて紙製ケース等の再使用を可能としたシ
ール部材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention contains a foaming agent to reduce the adhesive strength by heat treatment, and enables peeling without damaging the paper case or the like, enabling reuse of the paper case or the like. The present invention relates to a sealed member.
【0002】[0002]
【従来の技術】従来、フェルトや発泡体からなる多孔性
シール基材に両面粘着テープをラミネートしてなるシー
ル部材が知られていた。これは、トナーケース等の紙製
ケースのシールテープなどとして用いられている。2. Description of the Related Art Heretofore, there has been known a sealing member formed by laminating a double-sided adhesive tape on a porous sealing substrate made of felt or foam. It is used as a seal tape for a paper case such as a toner case.
【0003】しかしながら、接着力が大きくて紙製ケー
スより剥離する際に損傷を与え、紙製ケースを再使用で
きない問題点があった。また多孔性シール基材に粘着剤
を直接塗工することが困難で両面粘着テープとして多孔
性シール基材とラミネートするが、そのためにシール部
材の製造に多工程を要する難点があった。However, there is a problem that the adhesive strength is so great that it is damaged when peeled from the paper case, and the paper case cannot be reused. Further, it is difficult to directly apply the pressure-sensitive adhesive to the porous seal substrate, and the double-sided pressure-sensitive adhesive tape is laminated with the porous seal substrate. However, there is a problem in that the production of the seal member requires many steps.
【0004】[0004]
【発明が解決しようとする課題】本発明は、紙製ケース
等よりそれを損傷させずに剥離できてケースを再使用で
きるシール部材を得ることを課題とする。SUMMARY OF THE INVENTION It is an object of the present invention to obtain a seal member that can be peeled off from a paper case or the like without damaging it and the case can be reused.
【0005】[0005]
【課題を解決するための手段】本発明は、多孔性シール
基材の少なくとも片側に、必要に応じフィルム状中間層
を介して発泡剤含有の接着力低減型接着層を有すること
を特徴とするシール部材を提供するものである。The present invention is characterized in that an adhesive strength-reducing adhesive layer containing a foaming agent is provided on at least one side of a porous seal substrate, if necessary with a film-like intermediate layer interposed therebetween. A seal member is provided.
【0006】[0006]
【作用】接着力低減型接着層の加熱による接着力低減処
理により、含有する発泡剤が膨脹ないし発泡し、それに
より接着力が低下ないし消失する。その結果、ケース等
の被着体より容易に剥離でき、紙製ケースの場合でもそ
れを損傷させることがなく再使用が可能である。By the treatment for reducing the adhesive force by heating the adhesive force reducing type adhesive layer, the foaming agent contained therein expands or foams, whereby the adhesive force decreases or disappears. As a result, it can be peeled off easily from the adherend such as a case, and even in the case of a paper case, it can be reused without damaging it.
【0007】[0007]
【実施例】図1に本発明のシール部材を例示した。1が
多孔性シール基材、3が発泡剤含有の接着力低減型接着
層である。なお2は、必要に応じて設けられるフィルム
状中間層である。EXAMPLE FIG. 1 illustrates the seal member of the present invention. Reference numeral 1 is a porous seal base material, and 3 is a foaming agent-containing adhesive strength reduction type adhesive layer. In addition, 2 is a film-shaped intermediate | middle layer provided as needed.
【0008】多孔性シール基材としては、液体や粉体等
の目的とするシール対象に応じてその流出等を防止しう
るシール能を有する適宜な多孔構造体、例えばフェルト
や発泡体などが用いられる。厚さは、柔軟性等の点より
5mm以下、就中0.1〜1mmが一般的であるが、これに
限定されない。As the porous sealing base material, an appropriate porous structure having a sealing ability capable of preventing the liquid from flowing out or the like depending on the intended sealing target such as liquid or powder, for example, felt or foam is used. Be done. The thickness is generally 5 mm or less from the viewpoint of flexibility and the like, and particularly 0.1 to 1 mm, but the thickness is not limited to this.
【0009】接着力低減型接着層の形成には、適宜な接
着剤を用いることができ、一般には感圧接着剤などが用
いられる。その感圧接着剤としては、ゴム系感圧接着
剤、アクリル系感圧接着剤、スチレン・共役ジエンブロ
ック共重合体系感圧接着剤などの適宜なものを用いるこ
とができ、紫外線硬化型のものなども用いうる(特開昭
56−61468号公報、特開昭61−174857号
公報、特開昭63−17981号公報)。An appropriate adhesive can be used to form the adhesive force reduction type adhesive layer, and a pressure sensitive adhesive or the like is generally used. As the pressure-sensitive adhesive, an appropriate material such as a rubber-based pressure-sensitive adhesive, an acrylic pressure-sensitive adhesive, a styrene / conjugated diene block copolymer-based pressure-sensitive adhesive can be used. Etc. can be used (JP-A-56-61468, JP-A-61-174857, JP-A-63-17981).
【0010】また、融点が約200℃以下等の熱溶融性
樹脂を含有してクリープ性を改善したものや、常温では
接着力が小さくて加熱により充分な接着力が発現するよ
うにした熱時感圧接着剤なども用いうる(特公昭56−
13040号公報)。なお感圧接着剤は、必要に応じて
架橋剤、粘着付与樹脂、可塑剤、充填剤、老化防止剤な
どの適宜な添加剤を配合したものであってもよい。In addition, those having a melting point of about 200 ° C. or less to improve the creep property, and those which have a low adhesive strength at room temperature and exhibit sufficient adhesive strength by heating. A pressure sensitive adhesive or the like can also be used (Japanese Patent Publication No. 56-
13040). The pressure-sensitive adhesive may be a mixture of appropriate additives such as a cross-linking agent, a tackifying resin, a plasticizer, a filler, and an anti-aging agent, if necessary.
【0011】より具体的には例えば、天然ゴムや合成ゴ
ムをベースポリマーとするゴム系感圧接着剤、メチル
基、エチル基、プロピル基、ブチル基、2−エチルヘキ
シル基、イソオクチル基、イソノニル基、イソデシル
基、ドデシル基、ラウリル基、トリデシル基、ペンタデ
シル基、ヘキサデシル基、ヘプタデシル基、オクタデシ
ル基、ノナデシル基、エイコシル基の如き通例、炭素数
が20以下のアルキル基を有するアクリル酸ないしメタ
クリル酸等のアクリル酸系アルキルエステル、アクリル
酸、メタクリル酸、イタコン酸、アクリル酸ヒドロキシ
エチル、メタクリル酸ヒドロキシエチル、アクリル酸ヒ
ドロキシプロピル、メタクリル酸ヒドロキシプロピル、
N−メチロールアクリルアミド、アクリロニトリル、メ
タクリロニトリル、アクリル酸グリシジル、メタクリル
酸グリシジル、酢酸ビニル、スチレン、イソプレン、ブ
タジエン、イソブチレン、ビニルエーテルなどを成分と
するアクリル系ポリマーをベースポリマーとするアクリ
ル系感圧接着剤などがあげられる。More specifically, for example, a rubber-based pressure-sensitive adhesive containing natural rubber or synthetic rubber as a base polymer, methyl group, ethyl group, propyl group, butyl group, 2-ethylhexyl group, isooctyl group, isononyl group, Usually, such as isodecyl group, dodecyl group, lauryl group, tridecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group and eicosyl group, such as acrylic acid or methacrylic acid having an alkyl group having 20 or less carbon atoms, Acrylic acid alkyl ester, acrylic acid, methacrylic acid, itaconic acid, hydroxyethyl acrylate, hydroxyethyl methacrylate, hydroxypropyl acrylate, hydroxypropyl methacrylate,
Acrylic pressure-sensitive adhesive based on an acrylic polymer containing N-methylolacrylamide, acrylonitrile, methacrylonitrile, glycidyl acrylate, glycidyl methacrylate, vinyl acetate, styrene, isoprene, butadiene, isobutylene, vinyl ether, etc. Etc.
【0012】接着力低減処理前における接着力と接着力
低減処理による接着力の低下性のバランス、巻回物とす
る際や曲げ加工時等における被着体との密着追随性など
の点より好ましく用いうる感圧接着剤は、動的弾性率が
常温から150℃において50万〜1000万dyne/cm
2、好ましくは50万〜800万dyne/cm2の範囲にある
高弾性ポリマーをベースポリマーとするものである。ベ
ースポリマーとしてより好ましい高弾性ポリマーは、常
温から150℃における動的弾性率の変化率が小さいも
の、就中その変化程度が5倍以内のものである。It is preferable in terms of the balance between the adhesive force before the adhesive force reduction process and the adhesive force reduction property due to the adhesive force reduction process, and the adhesion followability with the adherend when it is used as a rolled material or during bending. The pressure-sensitive adhesive that can be used has a dynamic elastic modulus of 500,000 to 10,000,000 dyne / cm at room temperature to 150 ° C.
2 , preferably a highly elastic polymer in the range of 500,000 to 8,000,000 dyne / cm 2 as a base polymer. Highly elastic polymers that are more preferable as the base polymer are those having a small change rate of the dynamic elastic modulus from room temperature to 150 ° C., and in particular, those having a change degree of 5 times or less.
【0013】接着力低減型接着層は、接着剤に発泡剤を
配合することにより形成することができる。発泡剤の配
合により、加熱処理による含有発泡剤の膨脹ないし発泡
で接着力が低下ないし消失する接着層とすることができ
る。熱時感圧接着剤を用いた場合には、その接着剤の接
着処理温度よりも高温で膨脹ないし発泡する発泡剤が用
いられる。The adhesive strength reduction type adhesive layer can be formed by blending an adhesive with a foaming agent. By blending the foaming agent, it is possible to form an adhesive layer in which the adhesive strength is reduced or disappears due to expansion or foaming of the contained foaming agent by heat treatment. When the pressure sensitive adhesive at the time of heat is used, a foaming agent that expands or foams at a temperature higher than the bonding treatment temperature of the adhesive is used.
【0014】発泡剤の配合量は、接着力を低下させる程
度に応じて適宜に決定してよい。一般には、ベースポリ
マー100重量部あたり1〜100重量部、好ましくは
5〜50重量部、就中10〜40重量部配合される。The blending amount of the foaming agent may be appropriately determined depending on the degree to which the adhesive force is reduced. Generally, 1 to 100 parts by weight, preferably 5 to 50 parts by weight, especially 10 to 40 parts by weight are blended per 100 parts by weight of the base polymer.
【0015】用いる発泡剤については特に限定はなく、
種々の無機系や有機系の発泡剤を用いうる。無機系発泡
剤の代表例としては、炭酸アンモニウム、炭酸水素アン
モニウム、炭酸水素ナトリウム、亜硝酸アンモニウム、
水素化ホウ素ナトリウム、アジド類などがあげられる。The blowing agent used is not particularly limited,
Various inorganic or organic foaming agents can be used. As typical examples of the inorganic foaming agent, ammonium carbonate, ammonium hydrogen carbonate, sodium hydrogen carbonate, ammonium nitrite,
Examples thereof include sodium borohydride and azides.
【0016】有機系発泡剤の代表例としては、水、トリ
クロロモノフルオロメタンやジクロロモノフルオロメタ
ンの如き塩フッ化アルカン、アゾビスイソブチロニトリ
ルやアゾジカルボンアミド、バリウムアゾジカルボキシ
レートの如きアゾ系化合物、パラトルエンスルホニルヒ
ドラジドやジフェニルスルホン−3,3'−ジスルホニ
ルヒドラジド、4,4'−オキシビス(ベンゼンスルホ
ニルヒドラジド)、アリルビス(スルホニルヒドラジ
ド)の如きヒドラジン系化合物、ρ−トルイレンスルホ
ニルセミカルバジドや4,4'−オキシビス(ベンゼン
スルホニルセミカルバジド)の如きセミカルバジド系化
合物、5−モルホリル−1,2,3,4−チアトリアゾ
ールの如きトリアゾール系化合物、N,N'−ジニトロ
ソペンタメチレンテトラミンやN,N'−ジメチル−
N,N'−ジニトロソテレフタルアミドの如きN−ニト
ロソ系化合物などがあげられる。Typical examples of organic blowing agents include water, fluorinated alkanes such as trichloromonofluoromethane and dichloromonofluoromethane, and azo compounds such as azobisisobutyronitrile, azodicarbonamide and barium azodicarboxylate. Compounds, hydrazine compounds such as paratoluenesulfonyl hydrazide, diphenylsulfone-3,3′-disulfonylhydrazide, 4,4′-oxybis (benzenesulfonylhydrazide) and allylbis (sulfonylhydrazide), ρ-toluylenesulfonyl semicarbazide and Semicarbazide compounds such as 4,4′-oxybis (benzenesulfonyl semicarbazide), triazole compounds such as 5-morpholyl-1,2,3,4-thiatriazole, N, N′-dinitrosopentamethylenetetrami And N, N'-dimethyl -
Examples thereof include N-nitroso compounds such as N, N'-dinitrosoterephthalamide.
【0017】発泡剤をマイクロカプセル化してなる熱膨
脹性微粒子は、混合操作が容易であるなどの点より好ま
しく用いられる。熱膨脹性微粒子には、マイクロスフェ
ア(商品名、松本油脂社製)などの市販物もある。なお
本発明においては、必要に応じて発泡助剤を添加しても
よい。The heat-expandable fine particles obtained by encapsulating the foaming agent in microcapsules are preferably used because the mixing operation is easy. As the heat-expandable fine particles, there are commercially available products such as Microsphere (trade name, manufactured by Matsumoto Yushi Co., Ltd.). In the present invention, a foaming aid may be added if necessary.
【0018】シール部材の形成は、例えばセパレータ上
に塗工形成した発泡剤含有の接着力低減型接着層を多孔
性シール基材の少なくとも片側に移着する方法などの適
宜な方法で行うことができる。多孔性シール基材の接着
層付設面に、押出しフィルム化方式、フィルムのラミネ
ート方式などの適宜な方式でフィルム状中間層を設けた
場合には、接着剤の直接塗工方式で接着層を形成でき、
製造効率に優れる。設ける接着力低減型接着層の厚さ
は、適宜に決定してよい。一般には500μm以下、就
中5〜200μmとされる。The sealing member may be formed by an appropriate method such as a method of transferring the foaming agent-containing adhesive strength-reducing adhesive layer coated on the separator to at least one side of the porous seal substrate. it can. When a film-shaped intermediate layer is provided on the surface of the porous seal substrate on which the adhesive layer is attached by an appropriate method such as an extrusion film forming method or a film laminating method, the adhesive layer is formed by a direct adhesive coating method. You can
Excellent manufacturing efficiency. The thickness of the adhesive strength reduction type adhesive layer to be provided may be appropriately determined. Generally, the thickness is 500 μm or less, especially 5 to 200 μm.
【0019】また前記のフィルム状中間層の付設は、表
面平滑性に優れる接着層の形成に有効で、接着作業の安
定性の向上、ないしバラツキ防止に有利である。フィル
ム状中間層は、種々のポリマーや金属箔などにより形成
することができ、厚さは5〜500μmが一般的である
が、これに限定されない。なお多孔性シール基材の片側
に接着力低減型接着層を設けた場合、他方の側に接着力
低減型接着層でない通例の感圧性等の接着層を設けても
よい。Further, the provision of the film-like intermediate layer is effective for forming an adhesive layer having excellent surface smoothness, and is advantageous for improving the stability of the bonding work and preventing the dispersion. The film-like intermediate layer can be formed of various polymers or metal foils, and the thickness is generally 5 to 500 μm, but the thickness is not limited to this. When the adhesive force reduction type adhesive layer is provided on one side of the porous seal substrate, an adhesive layer having a pressure sensitive property which is not the adhesive force reduce type adhesive layer may be provided on the other side.
【0020】シール部材における接着力低減型接着層の
接着力の低減化、ないし消失化(接着力低減処理)は、
加熱により接着層中の発泡剤を膨脹、ないし発泡させる
ことにより行うことができる。加熱条件は、発泡剤の発
泡特性や、シール部材に用いた基材の耐熱性などにより
適宜に決定してよい。加熱処理は、使用目的に応じて適
宜な段階で行ってよい。The reduction or elimination of the adhesive force of the adhesive force reducing type adhesive layer in the seal member (adhesive force reducing treatment) is as follows.
It can be performed by expanding or foaming the foaming agent in the adhesive layer by heating. The heating conditions may be appropriately determined depending on the foaming characteristics of the foaming agent, the heat resistance of the base material used for the seal member, and the like. The heat treatment may be performed at an appropriate stage depending on the purpose of use.
【0021】本発明のシール部材は、被着体に貼着後そ
の貼着目的を終えたのち、あるいは収容物の交換や補充
の際などに被着体より容易に剥離できることが要求され
る種々の用途に好ましく用いることができる。その例と
しては、トナーケースや薬品瓶等の封止処理などがあげ
られ、特にシール部材の剥離時に損傷しやすい紙製製品
等に好ましく使用できる。The seal member of the present invention is required to be easily peeled off from the adherend after being adhered to the adherend and after the purpose of sticking is completed, or when the contents are replaced or replenished. Can be preferably used for Examples thereof include a sealing treatment of a toner case, a chemical bottle, and the like, which can be preferably used particularly for a paper product or the like which is easily damaged when the seal member is peeled off.
【0022】実施例1 アクリル酸ブチル100部(重量部、以下同じ)とアク
リル酸5部とアクリロニトリル10部の共重合体からな
る重量平均分子量120万のベースポリマー100部
に、熱膨脹性微粒子(マイクロスフェアF−80SD)
15部を配合してなる接着剤のトルエン溶液を、セパレ
ータの片面に塗工し乾燥処理して厚さ30μmの接着力
低減型接着層を形成し、それを厚さ50μmのナイロン
製フェルトの片面に移着してシール部材を得た。Example 1 100 parts of a base polymer having a weight average molecular weight of 1.2 million and consisting of a copolymer of 100 parts of butyl acrylate (parts by weight, the same applies hereinafter), 5 parts of acrylic acid and 10 parts of acrylonitrile, and heat-expandable fine particles (micro) Sphere F-80SD)
A toluene solution of an adhesive containing 15 parts is applied to one side of the separator and dried to form a 30 μm-thick adhesive strength-reducing adhesive layer, which is applied to one side of a 50 μm-thick nylon felt. To obtain a seal member.
【0023】実施例2 アクリルグラフトゴムを主ポリマーとし、テルペン系粘
着付与樹脂(Tg120℃)30部含有の感圧接着剤1
00部を含むトルエン溶液に、熱膨脹性微粒子(マイク
ロスフェアF−80SD)50部を配合してなる接着剤
を、厚さ50μmのナイロン製フェルトの片面にラミネ
ートした厚さ25μmのポリエステルフィルム層の上に
塗工し乾燥処理して厚さ30μmの接着力低減型接着層
を形成し、シール部材を得た。Example 2 Pressure-sensitive adhesive 1 containing acrylic graft rubber as a main polymer and 30 parts of a terpene-based tackifying resin (Tg 120 ° C.)
On a 25 μm-thick polyester film layer obtained by laminating 50 parts of heat-expandable fine particles (Microsphere F-80SD) in a toluene solution containing 00 parts on one side of a nylon felt having a thickness of 50 μm. Was applied to the above and dried to form a 30 μm thick adhesive strength-reducing type adhesive layer to obtain a seal member.
【0024】比較例1 熱膨脹性微粒子を配合しない接着剤を用いたほかは実施
例1に準じてシール部材を得た。Comparative Example 1 A sealing member was obtained in the same manner as in Example 1 except that an adhesive containing no heat-expandable fine particles was used.
【0025】比較例2 熱膨脹性微粒子を配合しない接着剤を用いたほかは実施
例2に準じてシール部材を得た。Comparative Example 2 A sealing member was obtained in the same manner as in Example 2 except that an adhesive containing no heat-expandable fine particles was used.
【0026】評価試験 接着力 実施例、比較例で得たシール部材における(接着力低減
型)接着層につき、ステンレス板(SUS 304 B
A仕上げ面)に対する常温(接着処理)又は150℃で
1分間の加熱処理(接着力低減処理)後における接着力
(180度ピール)をJIS Z 0237に準拠して
測定した。Evaluation Test Adhesive Strength A stainless steel plate (SUS 304 B) was used for the (adhesive strength reduction type) adhesive layers in the seal members obtained in Examples and Comparative Examples.
Adhesive strength (180 degree peel) after room temperature (adhesive treatment) or heat treatment (adhesive strength reduction treatment) at 150 ° C. for 1 minute with respect to A finished surface) was measured according to JIS Z 0237.
【0027】剥離性 実施例、比較例で得たシール部材を用いて前記に準じダ
ンボール箱の蓋部をシール接着処理したのち加熱処理
(接着力低減処理)し、ついでシール部材を剥離し、剥
離性を評価した。評価の基準は、ダンボール箱を形成す
る紙を破断、損傷なく剥がせた場合○、剥がし時にダン
ボール箱を形成する紙が破断、損傷した場合×とした。Peelability Using the sealing members obtained in Examples and Comparative Examples, the lid of the cardboard box was subjected to seal adhesion treatment according to the above, followed by heat treatment (adhesion reduction treatment), and then the seal member was peeled and peeled. The sex was evaluated. The evaluation criteria were as follows: ○ when the paper forming the cardboard box was broken and peeled without damage, and × when the paper forming the cardboard box was broken or damaged during peeling.
【0028】上記の結果を表1に示した。The above results are shown in Table 1.
【表1】 [Table 1]
【0029】[0029]
【発明の効果】本発明によれば、接着層が発泡剤を含有
して加熱処理によりその接着力を低下ないし消失するシ
ール部材を得ることができ、紙や発泡体等の破損しやす
い被着体の場合にもそれを損傷させずにスムーズに剥離
でき、作業の能率性に優れると共に、ケース等の被着体
の再使用を可能にすることができる。According to the present invention, it is possible to obtain a seal member whose adhesive layer contains a foaming agent and whose adhesive strength is reduced or eliminated by heat treatment, and which is easily adhered to paper or foam. In the case of a body, it can be peeled off smoothly without damaging it, and the work efficiency is excellent, and the adherend such as a case can be reused.
【図1】実施例の断面図FIG. 1 is a sectional view of an embodiment.
1:多孔性シール基材 2:フィルム状中間層 3:発泡剤含有の接着力低減型接着層 1: Porous seal substrate 2: Film-like intermediate layer 3: Foaming agent-containing adhesive strength reduction type adhesive layer
Claims (2)
泡剤含有の接着力低減型接着層を有することを特徴とす
るシール部材。1. A sealing member comprising a porous seal substrate and a foaming agent-containing adhesive strength-reducing adhesive layer on at least one side of the porous seal substrate.
の間にフィルム状中間層を有する請求項1に記載のシー
ル部材。2. The seal member according to claim 1, further comprising a film-like intermediate layer between the porous seal substrate and the adhesive force reduction type adhesive layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4084794A JP3059295B2 (en) | 1992-03-06 | 1992-03-06 | Seal member |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4084794A JP3059295B2 (en) | 1992-03-06 | 1992-03-06 | Seal member |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH05247413A true JPH05247413A (en) | 1993-09-24 |
JP3059295B2 JP3059295B2 (en) | 2000-07-04 |
Family
ID=13840610
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4084794A Expired - Lifetime JP3059295B2 (en) | 1992-03-06 | 1992-03-06 | Seal member |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3059295B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09235543A (en) * | 1996-02-29 | 1997-09-09 | Nitto Denko Corp | Sealing material |
US7611769B2 (en) | 2001-08-28 | 2009-11-03 | Boss Polymer Technologies Pty Ltd | Resilient product |
JP2018083883A (en) * | 2016-11-22 | 2018-05-31 | 中興化成工業株式会社 | Adhesive tape |
-
1992
- 1992-03-06 JP JP4084794A patent/JP3059295B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09235543A (en) * | 1996-02-29 | 1997-09-09 | Nitto Denko Corp | Sealing material |
US7611769B2 (en) | 2001-08-28 | 2009-11-03 | Boss Polymer Technologies Pty Ltd | Resilient product |
JP2018083883A (en) * | 2016-11-22 | 2018-05-31 | 中興化成工業株式会社 | Adhesive tape |
Also Published As
Publication number | Publication date |
---|---|
JP3059295B2 (en) | 2000-07-04 |
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