JPH04249143A - Synthetic-resin laminated foam and manufacture thereof - Google Patents
Synthetic-resin laminated foam and manufacture thereofInfo
- Publication number
- JPH04249143A JPH04249143A JP3013373A JP1337391A JPH04249143A JP H04249143 A JPH04249143 A JP H04249143A JP 3013373 A JP3013373 A JP 3013373A JP 1337391 A JP1337391 A JP 1337391A JP H04249143 A JPH04249143 A JP H04249143A
- Authority
- JP
- Japan
- Prior art keywords
- laminated foam
- synthetic resin
- synthetic
- resin laminated
- laminated
- 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
- 239000006260 foam Substances 0.000 title claims abstract description 36
- 229920003002 synthetic resin Polymers 0.000 title claims abstract description 31
- 239000000057 synthetic resin Substances 0.000 title claims abstract description 31
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 239000000203 mixture Substances 0.000 claims abstract description 13
- 239000004088 foaming agent Substances 0.000 claims abstract description 7
- 238000005187 foaming Methods 0.000 claims description 15
- 238000004132 cross linking Methods 0.000 claims description 10
- 238000003825 pressing Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 14
- 230000001070 adhesive effect Effects 0.000 abstract description 3
- 238000000197 pyrolysis Methods 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 14
- 239000004604 Blowing Agent Substances 0.000 description 7
- -1 ethylene- Ethylene Chemical group 0.000 description 7
- 150000001451 organic peroxides Chemical class 0.000 description 7
- 239000003431 cross linking reagent Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 4
- 239000005038 ethylene vinyl acetate Substances 0.000 description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 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
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
- 239000004156 Azodicarbonamide Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 2
- 235000019399 azodicarbonamide Nutrition 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000010894 electron beam technology Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000007500 overflow downdraw method Methods 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- 235000014692 zinc oxide Nutrition 0.000 description 2
- QEQBMZQFDDDTPN-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy benzenecarboperoxoate Chemical compound CC(C)(C)OOOC(=O)C1=CC=CC=C1 QEQBMZQFDDDTPN-UHFFFAOYSA-N 0.000 description 1
- KDGNCLDCOVTOCS-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy propan-2-yl carbonate Chemical compound CC(C)OC(=O)OOC(C)(C)C KDGNCLDCOVTOCS-UHFFFAOYSA-N 0.000 description 1
- RIPYNJLMMFGZSX-UHFFFAOYSA-N (5-benzoylperoxy-2,5-dimethylhexan-2-yl) benzenecarboperoxoate Chemical compound C=1C=CC=CC=1C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C1=CC=CC=C1 RIPYNJLMMFGZSX-UHFFFAOYSA-N 0.000 description 1
- BLKRGXCGFRXRNQ-SNAWJCMRSA-N (z)-3-carbonoperoxoyl-4,4-dimethylpent-2-enoic acid Chemical compound OC(=O)/C=C(C(C)(C)C)\C(=O)OO BLKRGXCGFRXRNQ-SNAWJCMRSA-N 0.000 description 1
- HSLFISVKRDQEBY-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)cyclohexane Chemical compound CC(C)(C)OOC1(OOC(C)(C)C)CCCCC1 HSLFISVKRDQEBY-UHFFFAOYSA-N 0.000 description 1
- AXRGJHZVODSOJJ-UHFFFAOYSA-N 1-tert-butylperoxy-3,5,5-trimethylhexane Chemical compound CC(C)(C)CC(C)CCOOC(C)(C)C AXRGJHZVODSOJJ-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- HQOVXPHOJANJBR-UHFFFAOYSA-N 2,2-bis(tert-butylperoxy)butane Chemical compound CC(C)(C)OOC(C)(CC)OOC(C)(C)C HQOVXPHOJANJBR-UHFFFAOYSA-N 0.000 description 1
- JPOUDZAPLMMUES-UHFFFAOYSA-N 2,2-bis(tert-butylperoxy)octane Chemical compound CCCCCCC(C)(OOC(C)(C)C)OOC(C)(C)C JPOUDZAPLMMUES-UHFFFAOYSA-N 0.000 description 1
- 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 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- BIISIZOQPWZPPS-UHFFFAOYSA-N 2-tert-butylperoxypropan-2-ylbenzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=CC=C1 BIISIZOQPWZPPS-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- 230000005865 ionizing radiation Effects 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 229920005670 poly(ethylene-vinyl chloride) Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- JIYXDFNAPHIAFH-UHFFFAOYSA-N tert-butyl 3-tert-butylperoxycarbonylbenzoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC(C(=O)OC(C)(C)C)=C1 JIYXDFNAPHIAFH-UHFFFAOYSA-N 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、合成樹脂積層発泡体お
よびその製造方法に関し、さらに詳しくは、層間の接着
性が改良され、製造方法も簡素化された合成樹脂積層発
泡体およびその製造方法に関する。[Field of Industrial Application] The present invention relates to a synthetic resin laminated foam and a method for producing the same, and more specifically, a synthetic resin laminated foam with improved interlayer adhesion and a simplified manufacturing method, and a method for producing the same. Regarding.
【0002】0002
【従来の技術】従来、例えば、発泡倍率の異なる層を2
層以上有する積層発泡体、あるいは2種以上の異種合成
樹脂発泡体層を有する積層発泡体などの合成樹脂積層発
泡体を製造する方法としては、予めそれぞれの発泡体を
作成した後、ラミネート加工する方法が知られている。[Prior Art] Conventionally, for example, two layers with different expansion ratios were used.
As a method for manufacturing a synthetic resin laminated foam such as a laminated foam having more than one layer or a laminated foam having two or more different types of synthetic resin foam layers, each foam is created in advance and then laminated. method is known.
【0003】ラミネート加工方法としては、通常、複数
の発泡体を熱融着する方法が採用されている。ところが
、従来の熱融着法では、図2に示すように、各層の積層
界面(層間)に明確な融着層が形成されるため、断面が
見苦しく、しかも融着不良などの品質不良の発生が見ら
れる。また、各発泡体を別個に製造した後に、熱融着を
行なう工程が必要であり、時間と費用がかかること、そ
の上、薄物の発泡体の積層が困難であること、等の問題
があった。[0003] As a laminating method, a method of heat-sealing a plurality of foam bodies is usually adopted. However, in the conventional heat fusion method, as shown in Figure 2, a clear fused layer is formed at the laminated interface (between layers) of each layer, resulting in an unsightly cross section and the occurrence of quality defects such as poor fusion. can be seen. In addition, a process of heat-sealing is required after each foam is manufactured separately, which is time-consuming and costly. Furthermore, there are problems such as the difficulty of laminating thin foams. Ta.
【0004】0004
【発明が解決しようとする課題】本発明の目的は、簡単
な操作により、層間の接着性が良好で、しかも外観美麗
な合成樹脂積層発泡体を提供することにある。また、本
発明の目的は、薄物であっても容易に積層発泡体を製造
できる方法を提供することにある。SUMMARY OF THE INVENTION An object of the present invention is to provide a synthetic resin laminated foam that can be easily operated, has good adhesion between layers, and has a beautiful appearance. Another object of the present invention is to provide a method for easily producing a laminated foam even if it is thin.
【0005】本発明者は、前記従来技術の有する問題点
を克服するために鋭意研究した結果、発泡前の発泡性合
成樹脂組成物シートの段階で、複数種のシートの加熱圧
着を行なって積層し、しかる後、これを架橋・発泡させ
ることにより、上記目的を達成できることを見いだし、
その知見に基づいて本発明を完成するに至った。[0005] As a result of intensive research in order to overcome the problems of the prior art, the inventor of the present invention conducted heat-pressure bonding of multiple types of sheets to laminate them at the stage of forming a foamable synthetic resin composition sheet before foaming. However, it was discovered that the above object could be achieved by crosslinking and foaming the material.
Based on this knowledge, we have completed the present invention.
【0006】[0006]
【課題を解決するための手段】かくして、本発明によれ
ば、熱分解型発泡剤を含有する発泡性合成樹脂組成物シ
ートを複数枚重ね合わせて加熱圧着し、しかる後、架橋
・発泡させることを特徴とする合成樹脂積層発泡体の製
造方法が提供される。また、本発明によれば、上記方法
により製造された合成樹脂積層発泡体が提供される。以
下、本発明について詳述する。[Means for Solving the Problems] Thus, according to the present invention, a plurality of foamable synthetic resin composition sheets containing a pyrolyzable foaming agent are superimposed and bonded under heat, and then crosslinked and foamed. Provided is a method for producing a synthetic resin laminated foam characterized by the following. Further, according to the present invention, there is provided a synthetic resin laminated foam manufactured by the above method. The present invention will be explained in detail below.
【0007】(発泡性合成樹脂組成物)本発明で用いる
合成樹脂としては、例えば、低密度ポリエチレン、中〜
高密度ポリエチレン、直鎖状低密度ポリエチレン、エチ
レン−酢酸ビニル共重合体、エチレン−塩化ビニル共重
合体、エチレン−メタクリレート共重合体、エチレン−
エチルアクリレート共重合体などのエチレン系重合体、
ポリプロピレン、ブテン−プロピレン共重合体、エチレ
ン−プロピレン共重合体などのポリプロピレン系重合体
、塩素化ポリエチレン、アイオノマー、クロルスルフォ
ン化ポリエチレン、およびこれらの混合物などのオレフ
ィン系樹脂を挙げることができる。(Foamable synthetic resin composition) Examples of the synthetic resin used in the present invention include low density polyethylene, medium to
High-density polyethylene, linear low-density polyethylene, ethylene-vinyl acetate copolymer, ethylene-vinyl chloride copolymer, ethylene-methacrylate copolymer, ethylene-
Ethylene polymers such as ethyl acrylate copolymers,
Examples include polypropylene polymers such as polypropylene, butene-propylene copolymer, and ethylene-propylene copolymer, olefin resins such as chlorinated polyethylene, ionomers, chlorosulfonated polyethylene, and mixtures thereof.
【0008】発泡性合成樹脂組成物は、合成樹脂に所望
発泡倍率により変量した熱分解型発泡剤を必須成分とし
て含有させ、有機過酸化物で架橋する場合には架橋剤と
して該有機過酸化物を含ませ、さらに、必要により発泡
助剤、架橋助剤、難燃剤、抗酸化剤、充填材、着色剤等
を加えたものである。[0008] The foamable synthetic resin composition contains as an essential component a thermally decomposable blowing agent that is varied depending on the desired expansion ratio in the synthetic resin, and when crosslinking with an organic peroxide, the organic peroxide is used as the crosslinking agent. In addition, a foaming aid, a crosslinking aid, a flame retardant, an antioxidant, a filler, a coloring agent, etc. are added as necessary.
【0009】本発明で使用する熱分解型発泡剤としては
、例えば、アゾジカルボンアミド、ジニトロソペンタメ
チレンテトラミン、オキシビスベンゼンスルホニルヒド
ラジド、アゾビスイソブチロニトリル、4,4′−オキ
シビスベンゼンスルホニルヒドラジド等、熱で分解し気
体を発生する各種の発泡剤を挙げることができる。熱分
解型発泡剤の使用割合は、所望倍率により変化するが、
一般的には、合成樹脂100重量部に対して1〜25重
量部である。Examples of the thermally decomposable blowing agent used in the present invention include azodicarbonamide, dinitrosopentamethylenetetramine, oxybisbenzenesulfonyl hydrazide, azobisisobutyronitrile, and 4,4'-oxybisbenzenesulfonyl. Examples include various blowing agents that decompose with heat and generate gas, such as hydrazide. The proportion of the pyrolytic blowing agent used varies depending on the desired magnification, but
Generally, the amount is 1 to 25 parts by weight per 100 parts by weight of the synthetic resin.
【0010】有機過酸化物で架橋する場合に用いる有機
過酸化物としては、例えば、1,1−ビス(t−ブチル
パーオキシ)シクロヘキサン、t−ブチルパーオキシマ
レイン酸、t−ブチルパーオキシ−3,5,5−トリメ
チルヘキサン、シクロヘキサンパーオキサイド、t−ブ
チルパーオキシアリルカーボネイト、t−ブチルパーオ
キシイソプロピルカーボネイト、2,5−ジメチル−2
,5−ジ(ベンゾイルパーオキシ)ヘキサン、2,2−
ビス(t−ブチルパーオキシ)オクタン、t−ブチルパ
ーオキシアセテート、2,2−ビス(t−ブチルパーオ
キシ)ブタン、t−ブチルパーオキシベンゾエート、n
−ブチル−4,4−ビス(t−ブチルパーオキシ)ベル
レート、ジt−ブチルパーオキシイソフタレート、メチ
ルエチルケトンパーオキサイド、ジクミルパーオキサイ
ド、2,5−ジメチル−2,5−ジ(t−ブチルパーオ
キシ)ヘキサン、α,α′−ビス(t−ブチルパーオキ
シ−m−イソプロピル)ベンゼン、t−ブチルクミルパ
ーオキサイド、ジ−t−ブチルパーオキサイド等を挙げ
ることができる。有機過酸化物を用いる場合には、通常
、合成樹脂100重量部に対して、0.3〜5重量部の
割合が好ましい。Examples of organic peroxides used in crosslinking with organic peroxides include 1,1-bis(t-butylperoxy)cyclohexane, t-butylperoxymaleic acid, t-butylperoxy- 3,5,5-trimethylhexane, cyclohexane peroxide, t-butylperoxyallyl carbonate, t-butylperoxyisopropyl carbonate, 2,5-dimethyl-2
, 5-di(benzoylperoxy)hexane, 2,2-
Bis(t-butylperoxy)octane, t-butylperoxyacetate, 2,2-bis(t-butylperoxy)butane, t-butylperoxybenzoate, n
-butyl-4,4-bis(t-butylperoxy)berlate, di-t-butylperoxyisophthalate, methyl ethyl ketone peroxide, dicumyl peroxide, 2,5-dimethyl-2,5-di(t-butyl) (peroxy)hexane, α,α'-bis(t-butylperoxy-m-isopropyl)benzene, t-butylcumyl peroxide, di-t-butyl peroxide, and the like. When using an organic peroxide, the proportion is usually preferably 0.3 to 5 parts by weight per 100 parts by weight of the synthetic resin.
【0011】本発明の発泡性合成樹脂組成物には、例え
ば、脂肪酸金属塩や亜鉛華等の発泡助剤、ジビニルベン
ゼン、トリメチロールプロパントリメタクリレート、ジ
エチレングリコールジメタクリレート、1,4−ポリブ
タジエン等の架橋助剤、難燃剤、充填材、抗酸化剤、着
色剤等を添加することができる。The foamable synthetic resin composition of the present invention includes, for example, foaming aids such as fatty acid metal salts and zinc white, and crosslinking agents such as divinylbenzene, trimethylolpropane trimethacrylate, diethylene glycol dimethacrylate, and 1,4-polybutadiene. Auxiliary agents, flame retardants, fillers, antioxidants, colorants, etc. can be added.
【0012】(合成樹脂積層発泡体の製造方法)熱分解
型発泡剤を含有する合成樹脂組成物を、合成樹脂が溶融
する温度以上、熱分解型発泡剤や架橋剤(有機過酸化物
)が分解する温度以下の範囲で混練し、シート成型機で
シート状に成形する。得られた複数枚のシートを、同様
に熱分解型発泡剤や架橋剤が分解する温度以下の温度(
通常、90〜140℃程度)で加熱圧着し、所定の厚み
の積層体とする。圧着する方法としては、例えば、プレ
スやカレンダー機で処理する方法が挙げられる。(Method for producing a synthetic resin laminated foam) A synthetic resin composition containing a pyrolytic blowing agent is heated to a temperature above the temperature at which the synthetic resin melts, and the pyrolytic blowing agent or crosslinking agent (organic peroxide) is Knead at a temperature below decomposition temperature and form into a sheet using a sheet molding machine. The resulting multiple sheets were heated to a temperature below the temperature at which the pyrolytic foaming agent and crosslinking agent decompose (
The laminate is bonded under heat at a temperature of about 90 to 140° C. to form a laminate having a predetermined thickness. Examples of the compression bonding method include a method using a press or a calendar machine.
【0013】図3は、油圧プレス中で加熱圧着する方法
を示す斜視図である。図4は、正面図である。アルミニ
ウム製スぺーサー4を置いたプレス台の上に重ね合わせ
た複数枚の発泡性合成樹脂組成物シート5を載せ、プレ
ス3,3で圧着すると、所望の厚み(スペーサーの厚み
)の発泡性積層シートを得ることができる。なお、各発
泡性シートは、熱分解型発泡剤や架橋剤が分解する温度
以下の温度に昇温しておく。FIG. 3 is a perspective view showing a method of heat-pressing in a hydraulic press. FIG. 4 is a front view. A plurality of stacked foamable synthetic resin composition sheets 5 are placed on a press stand on which an aluminum spacer 4 is placed, and when pressed with presses 3, 3, the desired thickness (thickness of the spacer) is achieved. A laminated sheet can be obtained. Note that each foamable sheet is heated to a temperature below the temperature at which the pyrolyzable foaming agent and the crosslinking agent decompose.
【0014】次いで、積層シートに、電離性放射線(電
子線または放射線)を照射して、発泡に必要な粘弾性を
得る架橋を樹脂に与えた後、熱分解型発泡剤を加熱分解
させ、気体を樹脂中に発生させて発泡せしめ、架橋積層
発泡体を得る。有機過酸化物により架橋させる場合には
、積層シートを発泡前に予備加熱して発泡に必要な粘弾
性を樹脂に与えた後、加熱発泡させるか、架橋と同時に
発泡させて架橋積層発泡体を得る。Next, the laminated sheet is irradiated with ionizing radiation (electron beam or radiation) to give the resin crosslinking that provides the viscoelasticity necessary for foaming, and then the pyrolytic foaming agent is thermally decomposed to form a gas. is generated in the resin and foamed to obtain a crosslinked laminated foam. When crosslinking with an organic peroxide, the laminated sheet is preheated before foaming to give the resin the viscoelasticity necessary for foaming, and then heated and foamed, or simultaneously crosslinked and foamed to form a crosslinked laminated foam. obtain.
【0015】図1は、本発明の方法により得られた積層
発泡体を示す略図である。予め加熱圧着して積層してか
ら架橋発泡させているため、熱融着層のない美麗な積層
発泡体とすることができ、しかも層間の接着性は、層間
での架橋が生じているため良好である。FIG. 1 is a schematic representation of a laminated foam obtained by the method of the invention. Since the foam is heat-pressed and laminated in advance and then cross-linked and foamed, it is possible to create a beautiful laminated foam without a heat-adhesive layer, and the adhesion between the layers is good due to the cross-linking between the layers. It is.
【0016】[0016]
【実施例】以下、本発明について、実施例および比較例
を挙げて具体的に説明するが、本発明は、これらの実施
例のみに限定されるものではない。[Examples] The present invention will be specifically explained below with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples.
【0017】[実施例1]低密度ポリエチレン(MI=
2.5、密度=0.922)100重量部に対して、熱
分解型発泡剤としてアゾジカルボンアミド15重量部、
発泡助剤として亜鉛華1重量部を添加し、ヘンシェルミ
キサーで混合した。この混合物を直径65mmの押出機
(L/D=26)に投入し、溶融混練してTダイから押
出し、厚み1.80mm幅450mmの発泡性合成樹脂
組成物シート(A)を作成した。押出機の温度条件は、
配合物投入側から130℃、135℃、140℃、金型
は125℃で、押出量は45kg/時間であった。同様
にして、厚み1.35mmの発泡性シート(B)を作成
した。[Example 1] Low density polyethylene (MI=
2.5, density = 0.922) 15 parts by weight of azodicarbonamide as a pyrolytic blowing agent,
1 part by weight of zinc white was added as a foaming aid and mixed using a Henschel mixer. This mixture was put into an extruder with a diameter of 65 mm (L/D=26), melt-kneaded, and extruded from a T-die to create a foamable synthetic resin composition sheet (A) with a thickness of 1.80 mm and a width of 450 mm. The temperature conditions of the extruder are:
The temperature was 130°C, 135°C, and 140°C from the compound input side, the temperature of the mold was 125°C, and the extrusion rate was 45 kg/hour. In the same manner, a foamable sheet (B) having a thickness of 1.35 mm was created.
【0018】発泡性シートAおよびBを切り取り、12
0℃に加熱してから、図3に示すプレス機に載せ、厚み
2.5mmのスペーサーを用いて、プレスして圧着した
。得られた発泡性積層シートに電子線を照射(200K
eV、4Mrad)して架橋し、ついで230℃に加熱
したオーブン中に導入し、加熱発泡させた。得られた積
層発泡体の発泡倍率は,A層およびB層ともに30cc
/gであった。積層発泡体の層間接着性は良好であり、
手で強く引き剥そうとしても剥れることはなかった。[0018] Cut out the foam sheets A and B, and
After heating to 0° C., it was placed on a press shown in FIG. 3, and pressed using a spacer having a thickness of 2.5 mm. The obtained foamable laminated sheet was irradiated with an electron beam (200K
eV, 4 Mrad) for crosslinking, and then introduced into an oven heated to 230° C. and heated and foamed. The foaming ratio of the obtained laminated foam is 30cc for both layers A and B.
/g. The interlayer adhesion of laminated foam is good;
Even when I tried to forcefully pull it off by hand, it did not come off.
【0019】[実施例2〜4]表1に示す合成樹脂を用
い、厚みおよび/または発泡倍率(発泡剤の添加量)を
変化させた以外は、実施例1と同様にして積層発泡体を
作成した。結果を表1に示す。なお、PE−EVAは、
ポリエチレン(PE)とエチレン−酢酸ビニル共重合体
(EVA;酢酸ビニル含有量19%、MI=2.5)と
の1:1の混合物である。[Examples 2 to 4] Laminated foams were produced in the same manner as in Example 1, except that the synthetic resins shown in Table 1 were used and the thickness and/or expansion ratio (amount of foaming agent added) was changed. Created. The results are shown in Table 1. In addition, PE-EVA is
It is a 1:1 mixture of polyethylene (PE) and ethylene-vinyl acetate copolymer (EVA; vinyl acetate content 19%, MI=2.5).
【0020】[0020]
【表1】
表1から明らかなように、同じ樹脂同士だけではなく、
実施例2のように異種の樹脂間においても良好な接着性
が認められた。[Table 1] As is clear from Table 1, not only the same resins but also
As in Example 2, good adhesion was observed even between different types of resins.
【0021】実施例3では、圧着における圧縮幅は、2
.7mmから2.5mmとわずかであるにもかかわらず
接着性は良好であった。In Example 3, the compression width in crimping is 2
.. Adhesion was good although the distance was small, from 7 mm to 2.5 mm.
【0022】実施例4は、シートAとシートBの発泡倍
率が異なっているが、それにもかかからず界面(接着面
)で剥離することなく良好な接着性が得られている。
これは、積層するシート同士の発泡倍率の多少のバラツ
キは、本発明の積層発泡法において問題にならないこと
を示している。In Example 4, although the foaming ratios of Sheet A and Sheet B are different, good adhesion was obtained without peeling at the interface (adhesive surface). This indicates that slight variations in the foaming ratios of laminated sheets do not pose a problem in the laminated foaming method of the present invention.
【0023】[0023]
【発明の効果】本発明の積層発泡体の製造方法によれば
、層間に融着層を持たないため、従来の熱融着によるも
のと比べて積層界面が美麗であり、かつ、層間での架橋
が起こっているため、強度的にも十分実用性能を有する
ものである。また、従来の熱融着法では困難であった薄
物の積層も可能である。[Effects of the Invention] According to the method for producing a laminated foam of the present invention, since there is no fused layer between the layers, the laminated interface is more beautiful than that produced by conventional heat fusion, and the laminated foam has a more beautiful appearance between the layers. Since crosslinking has occurred, it has sufficient practical performance in terms of strength. Furthermore, it is possible to laminate thin materials, which is difficult with conventional heat fusion methods.
【0024】しかも、従来の方法と比べて、発泡工程が
1回で済むため、製造に要する工程数、時間、費用を低
減することが可能となる。Moreover, compared to conventional methods, only one foaming step is required, making it possible to reduce the number of steps, time, and cost required for manufacturing.
【図1】本発明によって得られた積層発泡体の断面斜視
図。FIG. 1 is a cross-sectional perspective view of a laminated foam obtained by the present invention.
【図2】従来の熱融着によって得られた積層発泡体の断
面斜視図。FIG. 2 is a cross-sectional perspective view of a laminated foam obtained by conventional heat fusion.
【図3】本発明で用いた加熱圧着装置の斜視図。FIG. 3 is a perspective view of a thermocompression bonding device used in the present invention.
【図4】本発明で用いた加熱圧着装置の正面図。FIG. 4 is a front view of the thermocompression bonding device used in the present invention.
1 本発明によって得られた積層発泡体の接着面、2
従来の熱融着法によって得られた積層発泡体の融着
層、3 加熱圧着に用いた油圧プレス、4 厚さ2
.5mmのアルミニウム製スペーサー、5 発泡前の
発泡性合成樹脂シートA・Bを重ねたもの。1 Adhesive surface of the laminated foam obtained by the present invention, 2
Fused layer of laminated foam obtained by conventional heat fusing method, 3 Hydraulic press used for heat compression bonding, 4 Thickness 2
.. 5mm aluminum spacer, 5 Layered foamable synthetic resin sheets A and B before foaming.
Claims (2)
樹脂組成物シートを複数枚重ね合わせて加熱圧着し、し
かる後、架橋・発泡させることを特徴とする合成樹脂積
層発泡体の製造方法。1. A method for producing a synthetic resin laminated foam, which comprises stacking a plurality of sheets of a foamable synthetic resin composition containing a pyrolyzable foaming agent, heat-pressing them, and then crosslinking and foaming them. .
脂積層発泡体。2. A synthetic resin laminated foam obtained by the manufacturing method according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3013373A JPH04249143A (en) | 1991-02-04 | 1991-02-04 | Synthetic-resin laminated foam and manufacture thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3013373A JPH04249143A (en) | 1991-02-04 | 1991-02-04 | Synthetic-resin laminated foam and manufacture thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04249143A true JPH04249143A (en) | 1992-09-04 |
Family
ID=11831295
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3013373A Pending JPH04249143A (en) | 1991-02-04 | 1991-02-04 | Synthetic-resin laminated foam and manufacture thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04249143A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5407617A (en) * | 1991-10-31 | 1995-04-18 | Tarkett Pegulan Ag | Method of forming latex-, PVC- and plasticizer-free foamed floor or wall coverings |
JP2013221061A (en) * | 2012-04-16 | 2013-10-28 | Mitsufuku Industry Co Ltd | Rubber composition and method for producing the same |
-
1991
- 1991-02-04 JP JP3013373A patent/JPH04249143A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5407617A (en) * | 1991-10-31 | 1995-04-18 | Tarkett Pegulan Ag | Method of forming latex-, PVC- and plasticizer-free foamed floor or wall coverings |
JP2013221061A (en) * | 2012-04-16 | 2013-10-28 | Mitsufuku Industry Co Ltd | Rubber composition and method for producing the same |
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