JP2001198995A - Pad cushioning material - Google Patents
Pad cushioning materialInfo
- Publication number
- JP2001198995A JP2001198995A JP2000008630A JP2000008630A JP2001198995A JP 2001198995 A JP2001198995 A JP 2001198995A JP 2000008630 A JP2000008630 A JP 2000008630A JP 2000008630 A JP2000008630 A JP 2000008630A JP 2001198995 A JP2001198995 A JP 2001198995A
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- gel
- foam
- plasticizer
- pad
- 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
- 239000000463 material Substances 0.000 title claims abstract description 69
- 229920000642 polymer Polymers 0.000 claims abstract description 50
- 239000004014 plasticizer Substances 0.000 claims abstract description 26
- 239000000126 substance Substances 0.000 claims abstract description 13
- 239000000945 filler Substances 0.000 claims abstract description 11
- 229920001971 elastomer Polymers 0.000 claims abstract description 9
- 239000000806 elastomer Substances 0.000 claims abstract description 7
- 239000006260 foam Substances 0.000 claims description 24
- 239000007788 liquid Substances 0.000 claims description 20
- 239000006261 foam material Substances 0.000 claims description 16
- 238000004132 cross linking Methods 0.000 claims description 13
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000003431 cross linking reagent Substances 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- 125000003700 epoxy group Chemical group 0.000 claims description 8
- 125000003277 amino group Chemical group 0.000 claims description 7
- 125000000524 functional group Chemical group 0.000 claims description 6
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 5
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 claims description 3
- QQVHEQUEHCEAKS-UHFFFAOYSA-N diundecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCC QQVHEQUEHCEAKS-UHFFFAOYSA-N 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 239000004971 Cross linker Substances 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- 230000035882 stress Effects 0.000 description 16
- 239000006185 dispersion Substances 0.000 description 6
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 6
- 230000000740 bleeding effect Effects 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000012790 adhesive layer Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 230000035939 shock Effects 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000011243 crosslinked material Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001821 foam rubber Polymers 0.000 description 2
- 230000000116 mitigating effect Effects 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 229920001195 polyisoprene Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920006264 polyurethane film Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 2
- 150000003673 urethanes Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 description 1
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
- AHDSRXYHVZECER-UHFFFAOYSA-N 2,4,6-tris[(dimethylamino)methyl]phenol Chemical compound CN(C)CC1=CC(CN(C)C)=C(O)C(CN(C)C)=C1 AHDSRXYHVZECER-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- FUIQBJHUESBZNU-UHFFFAOYSA-N 2-[(dimethylazaniumyl)methyl]phenolate Chemical compound CN(C)CC1=CC=CC=C1O FUIQBJHUESBZNU-UHFFFAOYSA-N 0.000 description 1
- GTEXIOINCJRBIO-UHFFFAOYSA-N 2-[2-(dimethylamino)ethoxy]-n,n-dimethylethanamine Chemical compound CN(C)CCOCCN(C)C GTEXIOINCJRBIO-UHFFFAOYSA-N 0.000 description 1
- SHKUUQIDMUMQQK-UHFFFAOYSA-N 2-[4-(oxiran-2-ylmethoxy)butoxymethyl]oxirane Chemical compound C1OC1COCCCCOCC1CO1 SHKUUQIDMUMQQK-UHFFFAOYSA-N 0.000 description 1
- KUAUJXBLDYVELT-UHFFFAOYSA-N 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane Chemical compound C1OC1COCC(C)(C)COCC1CO1 KUAUJXBLDYVELT-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- VQVIHDPBMFABCQ-UHFFFAOYSA-N 5-(1,3-dioxo-2-benzofuran-5-carbonyl)-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(C(C=2C=C3C(=O)OC(=O)C3=CC=2)=O)=C1 VQVIHDPBMFABCQ-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- QORUGOXNWQUALA-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 Chemical compound N=C=O.N=C=O.N=C=O.C1=CC=C(C(C2=CC=CC=C2)C2=CC=CC=C2)C=C1 QORUGOXNWQUALA-UHFFFAOYSA-N 0.000 description 1
- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 description 1
- 101100219325 Phaseolus vulgaris BA13 gene Proteins 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- DSSXKBBEJCDMBT-UHFFFAOYSA-M lead(2+);octanoate Chemical compound [Pb+2].CCCCCCCC([O-])=O DSSXKBBEJCDMBT-UHFFFAOYSA-M 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000005474 octanoate group Chemical group 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- DYFXGORUJGZJCA-UHFFFAOYSA-N phenylmethanediamine Chemical compound NC(N)C1=CC=CC=C1 DYFXGORUJGZJCA-UHFFFAOYSA-N 0.000 description 1
- 229920003192 poly(bis maleimide) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000011257 shell material Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は椅子・マット等に使
用されるクッション材に係り、特に多方向への体圧分散
機能を備えたパッド・クッション材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cushioning material used for a chair or mat, and more particularly to a pad cushioning material having a function of dispersing body pressure in various directions.
【0002】[0002]
【従来の技術】従来、椅子・マット等に使用されるクッ
ション材に体圧分散機能を備えるためウレタンフォーム
やゴムフォームなどの軟質フォームが用いられていた
が、これら軟質フォーム単体を使用したクッション材
は、体圧を一方向(加圧方向)にしか吸収せず、体圧分
散性の効果が低いことから、車椅子使用者など長時間着
座する者の身体にかかる負担は避けられないものであっ
た。そこで軟質ゲル状物質を用いたり、あるいは反撥率
やポリマーの種類の異なるウレタンを積層したり、さら
にゲル状物質を軟質フォームに組み合わせたりすること
でより優れた体圧分散性を備えたクッション材が提案さ
れた。2. Description of the Related Art Conventionally, soft foams such as urethane foam and rubber foam have been used to provide a body pressure dispersing function to cushion materials used for chairs and mats. However, cushion materials using these soft foams alone have been used. Absorbs body pressure only in one direction (pressing direction) and has a low effect of dispersing body pressure, so that the burden on the body of a person who sits for a long time, such as a wheelchair user, is inevitable. Was. Therefore, cushion materials with better body pressure dispersibility can be obtained by using a soft gel material, laminating urethanes with different repulsion rates and polymer types, and combining the gel material with a soft foam. was suggested.
【0003】[0003]
【発明が解決しようとする課題】ところが、異種のウレ
タンを積層したクッション材は、一種のウレタン単独の
クッション材よりは体圧の加圧方向への吸収は優れてい
るものの、ウレタンの性質上、多方向への加圧分散性や
感温性に関する問題があり、クッション材として充分満
足できるものではない。However, the cushioning material in which different kinds of urethanes are laminated is superior to the cushioning material of a kind of urethane alone in the pressing direction of body pressure, but due to the properties of urethane, There are problems with pressure dispersibility and temperature sensitivity in multiple directions, and it is not sufficiently satisfactory as a cushion material.
【0004】また、クッション材に水を可塑剤とするゲ
ル状物質を使用したものは、使用時に含水率が変化する
という欠点がある。一方非水液体を可塑剤とするゲル状
物質を使用したものは、柔軟性は良好であるが、局部的
な応力分散性が乏しく、また使用者が満足しうる座り心
地を得るためには十分な厚みが必要となるため、重量が
大きくなり持ち運びが容易でないという不便さがあっ
た。また非水液体を可塑剤としたゲル状物質は、種類に
よっては可塑剤が表面に滲み出すブリードが生じ、接触
面を汚すという問題もあった。[0004] In addition, the use of a gel material containing water as a plasticizer for the cushioning material has a disadvantage that the water content changes during use. On the other hand, those using a gel-like substance using a non-aqueous liquid as a plasticizer have good flexibility but poor local stress dispersion, and are sufficient for the user to obtain a satisfactory sitting comfort. Because of the need for a large thickness, there is an inconvenience that the weight becomes large and it is not easy to carry. In addition, the gel-like substance using a non-aqueous liquid as a plasticizer has a problem in that, depending on the type, bleeding of the plasticizer onto the surface occurs, and the contact surface is soiled.
【0005】本発明は、このような問題点を改善するも
のであり、使用者の身体への負担を軽減すべく、多方向
応力分散性と低反発性を備えた軽量クッション材を提供
することを目的とする。SUMMARY OF THE INVENTION The present invention has been made to solve the above problems, and has as its object to provide a lightweight cushioning material having multidirectional stress dispersion and low resilience so as to reduce the burden on a user's body. With the goal.
【0006】[0006]
【課題を解決するための手段】上記目的を達成するため
に、本発明では液状高分子を架橋反応させることで形成
した分子網目間に可塑剤を含有させたゾルとゲル両特性
を持つゲル状物質と、軟質フォームとして低反撥フォー
ム材を積層させることで、極めて高い柔軟性、衝撃・振
動緩和性、応力分散性をクッション材に付与し、かつ、
ゲル材に高分子中空体あるいは高分子発泡体を充填する
ことで軽量化を実現できる。またゲル状物質の表面にエ
ラストマー製フィルムを貼着することで、ゲル状物質の
粘着性を阻止し、適度な応力分散を促進することができ
る。In order to achieve the above object, the present invention provides a gel-like polymer having both properties of a sol and a gel containing a plasticizer between molecular networks formed by a crosslinking reaction of a liquid polymer. By laminating a substance and a low repulsion foam material as a soft foam, extremely high flexibility, shock / vibration mitigation and stress dispersibility are imparted to the cushioning material, and
Filling the gel material with a polymer hollow body or a polymer foam can reduce the weight. Further, by sticking an elastomer film on the surface of the gel-like substance, it is possible to prevent the gel-like substance from sticking and to promote appropriate stress dispersion.
【0007】請求項2では、上記低反撥フォーム材とし
て反撥弾性率10%以下のウレタンフォームを使用する
ことで、より応力緩和に優れたパッド・クッション材を
提供する。According to a second aspect of the present invention, a pad cushion material excellent in stress relaxation is provided by using a urethane foam having a rebound resilience of 10% or less as the low rebound foam material.
【0008】また請求項3では、上記ゲル状物質とし
て、高分子中空体あるいは高分子発泡体の少なくとも一
種からなる充填材と、フタル酸ジイソデシルあるいはフ
タル酸ジウンデシルから選ばれた少なくとも一種の可塑
剤と、そしてイソシアネート基、エポキシ基、アミノ基
から選ばれた官能基を両末端を含めて2個以上有する架
橋剤とを配合した少なくとも末端か側鎖にOH基、CO
OH基、エポキシ基、アミノ基から選ばれた官能基を有
する液状高分子を架橋して得られたものを使用すること
により、低ブリード性を付与したパッド・クッション材
を提供できる。According to a third aspect of the present invention, as the gel-like substance, a filler made of at least one of a polymer hollow body and a polymer foam, and at least one plasticizer selected from diisodecyl phthalate or diundecyl phthalate are used. And a crosslinking agent having two or more functional groups selected from isocyanate groups, epoxy groups and amino groups at both ends, including at least both ends.
By using a material obtained by crosslinking a liquid polymer having a functional group selected from an OH group, an epoxy group, and an amino group, a pad cushion material having low bleeding properties can be provided.
【0009】[0009]
【発明の実施の形態】以下、本発明の実施例を図面を参
照にして説明する。図1は、本発明のパッド・クッショ
ン材1の断面図である。パッド・クッション材1は、高
分子中空体あるいは高分子発泡体からなる少なくとも一
種の充填材、可塑剤、そして架橋剤を配合した液状高分
子を架橋させて得られたゲル状物質4を外皮材としてエ
ラストマー製フィルム5で被覆したゲル材2と、低反撥
フォーム材3とが接着層6を介して積層されている。Embodiments of the present invention will be described below with reference to the drawings. FIG. 1 is a sectional view of a pad / cushion material 1 of the present invention. The pad / cushion material 1 is made of a gel material 4 obtained by crosslinking a liquid polymer in which at least one kind of filler consisting of a polymer hollow body or a polymer foam, a plasticizer, and a crosslinking agent are blended. A gel material 2 covered with an elastomer film 5 and a low repulsion foam material 3 are laminated via an adhesive layer 6.
【0010】なお、図1は1つの実施例の形態であっ
て、ゲル材2と低反撥フォーム材3との積層は複数積層
も可能で、かつこの基本層の繰り返しに限ることはな
く、例えば複数積層の最上層・最下層両面がゲル材2ま
たはその逆に低反撥フォーム材3でももちろんよい。ま
たゲル材2と低反撥フォーム材3の被積層面は、実施例
のように例えば両面テープや接着剤などの接着層6を介
して固着させてもよいし、熱着させてもよい。FIG. 1 shows an embodiment of the present invention. The lamination of the gel material 2 and the low repulsion foam material 3 can be a plurality of laminations, and is not limited to the repetition of this basic layer. Both the uppermost layer and the lowermost layer of the plurality of layers may be formed of the gel material 2 or the low repulsion foam material 3 on the contrary. Further, the laminated surface of the gel material 2 and the low repulsion foam material 3 may be fixed via an adhesive layer 6 such as a double-sided tape or an adhesive as in the embodiment, or may be heat-bonded.
【0011】低反撥フォームとは、反撥弾性率20%程
度以下のゴムフォームやウレタンフォーム等の軟質フォ
ームをさし、より良い体圧分散性を得るには、反撥弾性
率10%以下のウレタンフォームであることが好まし
い。[0011] The low rebound foam refers to a soft foam such as a rubber foam or urethane foam having a rebound resilience of about 20% or less, and a urethane foam having a rebound resilience of 10% or less in order to obtain better body pressure dispersibility. It is preferred that
【0012】本発明で架橋させる液状高分子は、少なく
とも末端か側鎖にOH基、COOH基、エポキシ基、ア
ミノ基から選ばれた官能基を有し、主鎖にポリブタジエ
ン、ポリイソプレン、ポリエーテルポリオール、ポリエ
ステルポリオールを有している。具体的には、ポリオキ
シアルキレンポリオール(住友バイエルウレタン製SB
U−Polyol−0265)、1,4ポリブタジエン
(出光石油化学社製R−45HT、R−15HT等)、
液状ポリイソプレンゴム(クラレ社製LIR−403、
410)等が挙げられる。The liquid polymer to be crosslinked in the present invention has a functional group selected from OH groups, COOH groups, epoxy groups and amino groups at least at the terminal or side chains, and has polybutadiene, polyisoprene, polyether in the main chain. It has a polyol and a polyester polyol. Specifically, a polyoxyalkylene polyol (SB manufactured by Sumitomo Bayer Urethane)
U-Polyol-0265), 1,4 polybutadiene (Idemitsu Petrochemical R-45HT, R-15HT, etc.),
Liquid polyisoprene rubber (KIRARE LIR-403,
410).
【0013】また、架橋剤としては、イソシアネート
基、エポキシ基、アミノ基から選ばれた官能基を両末端
を含めて2個以上有するものである。イソシアネート基
を有するものは、4,4’−ジフェニルメタンジイソシ
アネート、トルエン2,4’−ジイソシアネート、ヘキ
サメチレンジジイソシアネート、トリフェニルメタント
リイソシアネート、ポリアリールポリイソシアネートな
どがある。The crosslinking agent has two or more functional groups selected from isocyanate groups, epoxy groups, and amino groups, including both terminals. Those having an isocyanate group include 4,4'-diphenylmethane diisocyanate, toluene 2,4'-diisocyanate, hexamethylene didiisocyanate, triphenylmethane triisocyanate, and polyaryl polyisocyanate.
【0014】また、エポキシ基を有するものは、1,4
ブタンジオールジグリシジルエーテル、ネオペンチルグ
リコールジグリシジルエーテル、トリメチロールエタン
トリグリシジルエーテルなどがある。また、アミノ基を
有するものは、メタキシレンジアミン、ジエチレントリ
アミン、トリエチレンテトラミン、ジアミノフェニルメ
タンなどがある。更に、3,3’−4,4’ベンゾフェ
ノンテトラカルボン酸二無水物、M−フェビレン−ビス
マレイミドのような酸無水物がある。In addition, those having an epoxy group are 1,4
Butanediol diglycidyl ether, neopentyl glycol diglycidyl ether, trimethylolethane triglycidyl ether and the like. Those having an amino group include metaxylenediamine, diethylenetriamine, triethylenetetramine, and diaminophenylmethane. Further, there are acid anhydrides such as 3,3'-4,4'benzophenonetetracarboxylic dianhydride and M-fevirene-bismaleimide.
【0015】上記架橋剤の添加量は、液状高分子1当量
に対して0.4〜0.8当量である。0.4当量未満に
なると、架橋が不充分であり、架橋した材料が外皮材の
破れによって容易に流出してしまう。また、0.8当量
を越えると、架橋した材料が十分架橋して硬くなり、低
応力下での応力分散性が悪くなる。The amount of the crosslinking agent to be added is 0.4 to 0.8 equivalent to 1 equivalent of the liquid polymer. If it is less than 0.4 equivalent, the crosslinking is insufficient, and the crosslinked material easily flows out due to the tear of the outer skin material. On the other hand, if it exceeds 0.8 equivalents, the crosslinked material is sufficiently crosslinked and hardened, and the stress dispersibility under low stress is deteriorated.
【0016】可塑剤としては、上記液状高分子と相溶性
が良好な極性の可塑剤であればよく、中でも低ブリード
性を有するフタル酸系可塑剤が好ましい。具体的にはフ
タル酸ジイソデシル(分子量:447)あるいはフタル
酸ジウンデシル(分子量:475)から選ばれた少なく
とも1種であり、これらより分子量が小さなフタル酸系
可塑剤ではブリードアウトしやすく、一方これらより分
子量が大きなフタル酸系可塑剤ではゲル材との相溶性が
悪くなりゲルと可塑剤が分離しやすくなる。The plasticizer may be a polar plasticizer having good compatibility with the above liquid polymer, and a phthalic acid plasticizer having low bleeding property is preferable. Specifically, it is at least one selected from diisodecyl phthalate (molecular weight: 447) or diundecyl phthalate (molecular weight: 475), and a phthalic acid-based plasticizer having a smaller molecular weight is more likely to bleed out. A phthalic acid-based plasticizer having a large molecular weight has poor compatibility with the gel material, and the gel and the plasticizer are easily separated.
【0017】上記可塑剤の添加量としては、液状高分子
100重量部に対して50〜400重量部、50重量部
未満では、ゲル材の硬度が高くなり充分な応力分散性が
得られなくなったり、応力を除いた時の変形回復が遅い
という問題があり、400重量部を超えると、ゲル材中
に可塑剤が保持しきれなくなってゲルと可塑剤が分離し
やすくなったり、外皮材よりブリードアウトしやすくな
る。If the plasticizer is added in an amount of 50 to 400 parts by weight or less than 50 parts by weight based on 100 parts by weight of the liquid polymer, the hardness of the gel material becomes so high that sufficient stress dispersibility cannot be obtained. However, when the stress is removed, the deformation recovery is slow. When the amount exceeds 400 parts by weight, the plasticizer cannot be retained in the gel material, and the gel and the plasticizer are easily separated, and the bleeding is more difficult than the outer material. It becomes easy to out.
【0018】充填材である上記高分子中空体としては、
ポリアクリロニトリル、塩化ビニリデン、これらの共重
合体などを素材とした中空体であり、具体的にはこれら
の素材を隔壁として低沸点、炭化水素を内包する中空
体、あるいは作業性を向上させるために中空体の表面に
炭酸カルシウム、タルク等のゴム用充填材を付着させた
ものでもよい。また、高分子発泡体としては、独立気泡
をもったポリエチレン、ポリプロピレン、ポリウレタン
等の粉体である。これらの高分子中空体や高分子発泡体
の充填材は、少なくとも1種類使用することができ、具
体的には粒径や材料の相違するものを2種類以上使用す
ることができる。The hollow polymer body as the filler is as follows:
Polyacrylonitrile, vinylidene chloride, a hollow body made of such copolymers and the like, specifically, these materials as a partition, low boiling point, a hollow body containing hydrocarbons, or to improve workability A material in which a rubber filler such as calcium carbonate or talc is adhered to the surface of the hollow body may be used. The polymer foam is a powder of polyethylene, polypropylene, polyurethane or the like having closed cells. At least one kind of filler for these polymer hollow bodies and polymer foams can be used. Specifically, two or more kinds of fillers having different particle diameters and materials can be used.
【0019】上記高分子中空体や高分子発泡体の粒径は
2mm以下、好ましくは0.5mm以下である。粒径が
2mmを超えると、高分子中空体や高分子発泡体が液状
高分子、可塑剤等と分離してしまい、均質なゲル材にな
らず、また柔軟性が失われ十分な応力分散能力や振動、
衝撃緩和性が発揮できない。高分子中空体あるいは高分
子発泡体の添加量の体積分率は10〜80%である。も
し体積分率が10%未満になると、十分な軽量化効果が
得られず、一方80%を超えると、硬度が高くなりすぎ
るため、またゲル材の伸びが小さくなり、変形に対する
回復性も低下するため、十分な振動、衝撃緩和性、応力
分散性が発揮できない。The particle diameter of the polymer hollow body or the polymer foam is 2 mm or less, preferably 0.5 mm or less. When the particle size exceeds 2 mm, the polymer hollow body or polymer foam is separated from the liquid polymer, plasticizer, etc., and does not become a homogeneous gel material, and also loses flexibility and has sufficient stress dispersion ability. And vibration,
Cannot exhibit impact relaxation. The volume fraction of the added amount of the polymer hollow body or the polymer foam is 10 to 80%. If the volume fraction is less than 10%, a sufficient weight-reducing effect cannot be obtained, while if it exceeds 80%, the hardness becomes too high, the elongation of the gel material becomes small, and the recovery from deformation also decreases. Therefore, sufficient vibration, shock relaxation and stress dispersibility cannot be exhibited.
【0020】上記高分子中空体や高分子発泡体からなる
充填材は、比重が非常に小さいために飛散しやすく取り
扱いが困難であることから、予め適量の可塑剤と混合
し、充填材可塑剤混合物として使用してもよい。Since the filler made of the above-mentioned hollow polymer or foamed polymer is very small in specific gravity and easily scattered, it is difficult to handle it. It may be used as a mixture.
【0021】触媒としては、トリエチルアミン、N,
N,N’,N’−テトラメチルエチルジアミン、テトラ
メチルグアニジン、トリエチレンジアミン、ジメチルア
ミノエタノール、ビス(2−ジメチルアミノエチル)エ
ーテル、トリス(ジメチルアミノメチル)フェノール、
ジメチルアミノメチルフェノール等のアミン、あるいは
スタナスオクトエート、ジブチルチンジアセテート、ジ
ブリルチンジラウレート、ジブリルチンマーカブチド、
オクチン酸鉛等の有機錫化合物がある。As the catalyst, triethylamine, N,
N, N ′, N′-tetramethylethyldiamine, tetramethylguanidine, triethylenediamine, dimethylaminoethanol, bis (2-dimethylaminoethyl) ether, tris (dimethylaminomethyl) phenol,
Amines such as dimethylaminomethylphenol, or stannas octoate, dibutyltin diacetate, dibrilltin dilaurate, dibriltin carbubutide,
There are organotin compounds such as lead octoate.
【0022】上記触媒の添加量は、特に液状高分子をイ
ソシアネート基を有する架橋剤により架橋反応させる場
合には、液状高分子100重量部に対して、触媒0.0
05〜3重量部であり、また液状高分子をエポキシ基を
有する架橋剤により架橋反応させる場合には、液状高分
子100重量部に対して、触媒10〜30重量部であ
る。この範囲外においては、架橋が不充分でゲル材が形
成されず、また架橋反応が早くなり過ぎて、ゲル硬度の
バラツキが大きくなる。The amount of the catalyst to be added is, for example, when the liquid polymer is subjected to a cross-linking reaction with a cross-linking agent having an isocyanate group, based on 100 parts by weight of the liquid polymer.
In the case where the liquid polymer is subjected to a crosslinking reaction with a crosslinking agent having an epoxy group, the catalyst is used in an amount of 10 to 30 parts by weight based on 100 parts by weight of the liquid polymer. Outside this range, crosslinking is insufficient and a gel material is not formed, and the crosslinking reaction is too fast, resulting in a large variation in gel hardness.
【0023】また、本発明では、上記添加剤以外に、例
えばヒンダートフェノール系の酸化防止剤、例えばベン
ゾフェノン系もしくはベンゾトリアゾール系の紫外線吸
収剤、例えばアルキル酸エステルナトリウム等の界面活
性剤、あるいは例えばペンタクロロフェノール、銅−8
−ヒドロキシキノリン等の防黴剤を単体または混合して
添加することができる。In the present invention, in addition to the above additives, for example, a hindered phenol-based antioxidant, for example, a benzophenone-based or benzotriazole-based ultraviolet absorber, for example, a surfactant such as sodium alkyl ester, or Pentachlorophenol, copper-8
-A fungicide such as hydroxyquinoline can be added alone or as a mixture.
【0024】応力分散性ゲル状物質の製造方法として
は、上記液状高分子に、可塑剤および光安定剤を添加
し、その後架橋剤、触媒を加えて攪拌機にて均一に混合
する。その後更に高分子中空体や高分子発泡体もしくは
充填材可塑剤混合物を添加して均一に混合し、十分に脱
水する。これをエラストマー製フィルムからなる外皮材
を敷設した型に流し込み、20〜80°Cで1〜120
分間加熱して架橋した後、10〜50°Cにて1〜24
時間熟成する。As a method for producing the stress-dispersing gel-like substance, a plasticizer and a light stabilizer are added to the above liquid polymer, and then a crosslinking agent and a catalyst are added, followed by uniform mixing with a stirrer. Thereafter, a polymer hollow body, a polymer foam or a filler plasticizer mixture is further added and uniformly mixed, followed by sufficient dehydration. This is poured into a mold in which a skin material made of an elastomeric film is laid, and at 120-80 ° C., 1-120.
After heating and cross-linking for 10 minutes,
Aging time.
【0025】エラストマー製フィルムからなる外皮材
は、少なくとも応力がかかる負荷面に被覆してより一層
オイルのブリードアウトを防止することにあり、伸縮性
に富んだ厚さ30〜200μmのポリエステルポリウレ
タンフィルムが、応力分散性材料の粘着性を阻止すると
ともに、適度な応力分散を促進するうえで、好ましい。
ポリエーテルポリウレタンフィルムの場合には、上記オ
イルにより膨潤し、外皮材表面に著しくオイルのブリー
ドアウトを生じる。The outer shell material made of an elastomer film is used to coat at least the load surface to which stress is applied so as to further prevent oil bleed-out, and a highly stretchable polyester polyurethane film having a thickness of 30 to 200 μm is used. This is preferable because it prevents adhesion of the stress dispersing material and promotes appropriate stress dispersion.
In the case of a polyether polyurethane film, it swells due to the above oil, and causes significant bleed out of the oil on the surface of the skin material.
【0026】[0026]
【実施例】次に、本発明を具体的な実施例により更に詳
細に説明する。 実施例,比較例 紙に剥離可能に積層されたウレタンフィルムを寸法設定
して裁断し、これを395mm×395mm×15mm
の寸法の寸法をもつ型に設定する。次いで、表1に示す
材料のうち、高分子中空体可塑剤混合物を除く配合物を
攪拌機に投入し、均一に混合した。その混合物を、減圧
乾燥機にて1torr以下で60分間脱水した後、高分
子中空体可塑剤混合物を添加し攪拌機にてさらに混合
し、これを型に流し込み、80°Cで60分間加熱して
架橋させた後、40°Cにて24時間熟成してゲル状物
質を得た。続いて、このゲル状物質裏面に接着剤を塗布
した後、エラストマー製フィルムで裏面を被覆して、ゲ
ル材を作製した。このようにして予め得たゲル材と寸法
395mm×395mm×10mmの低反撥ウレタンフ
ォーム材を、両面接着テープを介して一層積層し、パッ
ド・クッション材を作製した。Next, the present invention will be described in more detail with reference to specific examples. Examples and Comparative Examples A urethane film laminated releasably on paper was cut out by setting dimensions, and this was cut into a piece of 395 mm × 395 mm × 15 mm.
Set to a mold with dimensions of Next, of the materials shown in Table 1, the compounds except the polymer hollow body plasticizer mixture were charged into a stirrer and uniformly mixed. After dehydrating the mixture with a reduced pressure dryer at 1 torr or less for 60 minutes, a polymer hollow body plasticizer mixture was added, and the mixture was further mixed with a stirrer, poured into a mold, and heated at 80 ° C. for 60 minutes. After crosslinking, the mixture was aged at 40 ° C. for 24 hours to obtain a gel substance. Subsequently, after applying an adhesive to the back surface of the gel-like substance, the back surface was covered with an elastomer film to prepare a gel material. The gel material thus obtained and the low-repulsion urethane foam material having a size of 395 mm × 395 mm × 10 mm were further laminated with a double-sided adhesive tape to prepare a pad cushion material.
【0027】[0027]
【表1】 [Table 1]
【0028】また、比較例,として、実施例の積
層体と同じ寸法(395mm×395mm×25mm)
の低反撥ウレタンフォーム単体、ゲル材単体の2サンプ
ルを用意し、実施例との比較検討を行った。As a comparative example, the same dimensions (395 mm × 395 mm × 25 mm) as those of the laminate of the example were used.
2 samples of low repulsion urethane foam alone and gel material alone were prepared and compared with the examples.
【0029】体圧分散測定方法としては、車椅子のキャ
ンバス上に実施例、比較例のサンプルをそれぞれ
乗せ、被験者(体重約60kg)が座り、座った直後
(15秒以内)と600秒後の体圧分布(最大圧力、平
均圧力)を3次元体圧測定装置FSA(VERG社)に
より測定した。結果を表2に示す。As a method of measuring body pressure dispersion, the samples of Examples and Comparative Examples were placed on a canvas of a wheelchair, and a subject (body weight: about 60 kg) sat, immediately after sitting (within 15 seconds) and after 600 seconds. The pressure distribution (maximum pressure, average pressure) was measured by a three-dimensional body pressure measuring device FSA (VERG). Table 2 shows the results.
【0030】[0030]
【表2】 [Table 2]
【0031】この結果から、ゲル材と低反撥フォーム材
とを積層することで、ゲル材単独、低反撥フォーム材単
独のクッション材にくらべ、衝撃緩和、体圧分散性に優
れていることが分かる。また外皮材表面へのオイルのブ
リードアウトもなく、使用者の官能評価も高かった。From these results, it can be seen that the lamination of the gel material and the low repulsion foam material is superior to the cushion material of the gel material alone or the low repulsion foam material alone in the impact relaxation and body pressure dispersibility. . In addition, there was no bleed-out of oil to the surface of the skin material, and the sensory evaluation of the user was high.
【0032】[0032]
【発明の効果】以上のように本願の発明では、液状高分
子を架橋反応させることで形成した分子網目間に可塑剤
を含有させたゾルとゲル両特性を持つゲル材と、低反撥
フォーム材を積層させることで、ゲル材、低反撥フォー
ム材夫々単独のパッド・クッション材よりも更に高い柔
軟性、衝撃・振動緩和性、応力分散性を有するパッド・
クッション材を実現することができ、かつ、ゲル材に高
分子中空体あるいは高分子発泡体を充填することにより
軽量化を実現できる。As described above, according to the present invention, a gel material having both characteristics of a sol and a gel containing a plasticizer between molecular networks formed by a crosslinking reaction of a liquid polymer, and a low repulsion foam material By laminating a pad, the pad material has higher flexibility, shock / vibration mitigation, and stress dispersibility than the pad / cushion material of the gel material and low repulsion foam material, respectively.
A cushion material can be realized, and the gel material is filled with a polymer hollow body or a polymer foam to reduce the weight.
【0033】また請求項2では、低反撥フォーム材とし
て反撥弾性率10%以下のウレタンフォームを使用する
ことでより一層の低反撥性・応力分散性を得ることがで
きる。According to the second aspect of the invention, by using a urethane foam having a rebound resilience of 10% or less as the low rebound foam material, it is possible to obtain much lower rebound and stress dispersibility.
【0034】さらに請求項3では、ゲル状物質を構成す
る可塑剤、架橋剤、そして液状高分子を特定すること
で、低ブリード性をクッション材に付与することができ
る。Further, in the third aspect, by specifying a plasticizer, a cross-linking agent, and a liquid polymer constituting the gel-like substance, low bleeding property can be imparted to the cushion material.
【図1】本発明のパッド・クッション材の断面図であ
る。FIG. 1 is a sectional view of a pad cushion material of the present invention.
1 パッド・クッション材 2 ゲル材 3 低反撥フォーム材 4 ゲル状物質 5 エラストマー製フィルム 6 接着層 DESCRIPTION OF SYMBOLS 1 Pad cushion material 2 Gel material 3 Low repulsion foam material 4 Gel substance 5 Elastomer film 6 Adhesive layer
フロントページの続き Fターム(参考) 4F100 AH02A AH02H AH03A AH03H AK01A AK28 AK29 AK41 AK51D AK54 AL09B AL09C AT00B AT00C BA04 BA07 BA10B BA10D BA13 CA02A CA04A CA23A CB00 DD31B DD31C DJ01 DJ01A DJ01D EJ05A GB81 JK07D JK10 JK11 JK13 JK17 JL03 JM01A JM10A YY00D Continued on front page F-term (reference) 4F100 AH02A AH02H AH03A AH03H AK01A AK28 AK29 AK41 AK51D AK54 AL09B AL09C AT00B AT00C BA04 BA07 BA10B BA10D BA13 CA02A CA04A CA23A CB00 DD31B DD31C DJ01K01 J01J01J01 J01J01
Claims (3)
外皮材で被覆したゲル材と低反撥フォーム材とが積層さ
れていて、且つ、前記ゲル状物質が、高分子中空体ある
いは高分子発泡体の少なくとも一種からなる充填材、可
塑剤、そして架橋剤を配合した液状高分子を架橋させた
ものであることを特徴とするパッド・クッション材。1. A gel material in which a gel material is coated with an envelope of an elastomer film and a low repulsion foam material are laminated, and the gel material is a polymer hollow body or a polymer foam. A pad / cushion material obtained by crosslinking a liquid polymer containing at least one filler, a plasticizer, and a crosslinking agent.
0%以下のウレタンフォーム材であることを特徴とする
請求項1記載のパッド・クッション材。2. The low rebound foam material has a rebound resilience of 1
The pad / cushion material according to claim 1, wherein the urethane foam material is 0% or less.
鎖にOH基、COOH基、エポキシ基、アミノ基から選
ばれた官能基を有する液状高分子に、高分子中空体ある
いは高分子発泡体の少なくとも一種からなる充填材と、
フタル酸ジイソデシルあるいはフタル酸ジウンデシルか
ら選ばれた少なくとも一種の可塑剤と、そしてイソシア
ネート基、エポキシ基、アミノ基から選ばれた官能基を
両末端を含めて2個以上有する架橋剤とを配合したもの
を架橋させたものである請求項1又は請求項2記載のパ
ッド・クッション材。3. The liquid polymer having a functional group selected from an OH group, a COOH group, an epoxy group, and an amino group at least at a terminal or a side chain thereof, wherein the gel-like substance is a polymer hollow body or a polymer foam. A filler consisting of at least one of
A blend of at least one plasticizer selected from diisodecyl phthalate or diundecyl phthalate, and a crosslinking agent having two or more functional groups selected from isocyanate groups, epoxy groups, and amino groups at both ends. 3. The pad / cushion material according to claim 1, wherein the pad / cushion material is obtained by crosslinking.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000008630A JP3507385B2 (en) | 2000-01-18 | 2000-01-18 | Pad cushion material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000008630A JP3507385B2 (en) | 2000-01-18 | 2000-01-18 | Pad cushion material |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2001198995A true JP2001198995A (en) | 2001-07-24 |
JP3507385B2 JP3507385B2 (en) | 2004-03-15 |
Family
ID=18536872
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2000008630A Expired - Fee Related JP3507385B2 (en) | 2000-01-18 | 2000-01-18 | Pad cushion material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3507385B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20220143271A (en) * | 2021-04-16 | 2022-10-25 | 주식회사 불스원 | Method for manufacturing bedding filler using gel cushion |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070226911A1 (en) * | 2006-04-03 | 2007-10-04 | Dreamwell, Ltd | Mattress or mattress pad with gel section |
-
2000
- 2000-01-18 JP JP2000008630A patent/JP3507385B2/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20220143271A (en) * | 2021-04-16 | 2022-10-25 | 주식회사 불스원 | Method for manufacturing bedding filler using gel cushion |
KR102476869B1 (en) | 2021-04-16 | 2022-12-14 | 주식회사 불스원 | Method for manufacturing bedding filler using gel cushion |
Also Published As
Publication number | Publication date |
---|---|
JP3507385B2 (en) | 2004-03-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US10435529B2 (en) | Air-permeable sponge composition and method for preparing air-permeable sponge by using the same | |
RU2551502C2 (en) | Method for producing elastic urethane foam and urethane foam produced by this method | |
CN1328037C (en) | Manufacturing process of polyurethane foam sheet and layered sheet using the same | |
TWI616474B (en) | Polyoxymethylene resin foam and sealing material | |
US20160068646A1 (en) | Method of producing polyurethane foam for cosmetic application and polyurethane foam for cosmetic application | |
KR20160004813A (en) | Ultra light polyurethane artificial leather composition | |
CN110283293A (en) | The imitative latex polyurethane flexible foam prepared using terminal isocyanate group performed polymer | |
JPWO2009119752A1 (en) | Solventless polyurethaneurea foam sheet, method for producing the same, and synthetic leather | |
JP2001198995A (en) | Pad cushioning material | |
JP5681981B2 (en) | Urethane foam sheet and manufacturing method thereof | |
JPWO2021010487A1 (en) | Shock absorbing sheet, adhesive tape and display device | |
JP2005052181A (en) | Cushioning material | |
KR101730055B1 (en) | Polyurethane resin composition and polyurethane mounting pad | |
US10813469B2 (en) | Cooling support cushion and method of producing the same | |
JPH1015959A (en) | Sheet material equipped with impact relaxing properties and stress dispersibiity and its production | |
CN113930001A (en) | Low-odor polyethylene foam material with thermal bonding performance and preparation method thereof | |
JP2011178951A (en) | Foamed polyurethane and method for producing the same and vibration insulator for automobile composed of foamed polyurethane | |
JPH10204283A (en) | Low bleeding stress dispersion gel material | |
JPH1072537A (en) | Stress-dispersible material reduced in weight | |
JP2021172731A (en) | Impact absorbing sheet, adhesive tape, and display device | |
TW513459B (en) | Polyurethane foam composition derived from a reaction mixture, the preparation process thereof, and polyurethane foam articles containing the same | |
JPH09143309A (en) | Lightweight stress dispersing gel material | |
KR102447348B1 (en) | a double layered matt for preventing interformational noise and bang | |
JPH1087871A (en) | Shock buffering material | |
JP2005052182A (en) | Body pressure dispersing mat |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20031216 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20031218 |
|
LAPS | Cancellation because of no payment of annual fees |