JP4166502B2 - Molding method of open cell foam - Google Patents
Molding method of open cell foam Download PDFInfo
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- JP4166502B2 JP4166502B2 JP2002128937A JP2002128937A JP4166502B2 JP 4166502 B2 JP4166502 B2 JP 4166502B2 JP 2002128937 A JP2002128937 A JP 2002128937A JP 2002128937 A JP2002128937 A JP 2002128937A JP 4166502 B2 JP4166502 B2 JP 4166502B2
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- molding
- open cell
- open
- cell foam
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- 238000000465 moulding Methods 0.000 title claims description 35
- 239000006260 foam Substances 0.000 title claims description 25
- 238000000034 method Methods 0.000 title claims description 25
- 229920002943 EPDM rubber Polymers 0.000 claims 1
- 230000001413 cellular effect Effects 0.000 claims 1
- 210000004027 cell Anatomy 0.000 description 23
- -1 polyethylene Polymers 0.000 description 12
- 229920001971 elastomer Polymers 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 239000005060 rubber Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 238000005187 foaming Methods 0.000 description 7
- 239000004088 foaming agent Substances 0.000 description 7
- 235000013399 edible fruits Nutrition 0.000 description 6
- 229920000098 polyolefin Polymers 0.000 description 5
- 210000005056 cell body Anatomy 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920005672 polyolefin resin Polymers 0.000 description 3
- 239000010734 process oil Substances 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000011162 core material Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 235000012055 fruits and vegetables Nutrition 0.000 description 2
- 230000005865 ionizing radiation Effects 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- 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
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- ZUGOSPHJWZAGBH-UHFFFAOYSA-N CO[SiH](OC)C=C Chemical compound CO[SiH](OC)C=C ZUGOSPHJWZAGBH-UHFFFAOYSA-N 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 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
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 229920003020 cross-linked polyethylene Polymers 0.000 description 1
- 239000004703 cross-linked polyethylene Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000010097 foam moulding Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- ALIFPGGMJDWMJH-UHFFFAOYSA-N n-phenyldiazenylaniline Chemical compound C=1C=CC=CC=1NN=NC1=CC=CC=C1 ALIFPGGMJDWMJH-UHFFFAOYSA-N 0.000 description 1
- 150000002832 nitroso derivatives Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Images
Landscapes
- Buffer Packaging (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
Description
【0001】
【発明の属する技術分野】
本発明は、果物、野菜等の保持材やクッション材に使用される連続気泡発泡体の成形方法に関するものである。
【0002】
【従来の技術】
従来、発泡体の成形方法は、目的とする形状に合わせて熱圧成形などの方法で、加熱して成形していた。例えば、(1)ポリオレフィン又はポリオレフィンとこれに重合可能なゴム、プラスチックとの混合物の架橋発泡体の1片又は2片以上を、金型内に於いてポリオレフィンの軟化点以上の温度に加熱しつつ一方向より20%以上圧縮し、次で圧力を加えたまま冷却する成形方法(特公昭52−49022号公報)、(2)ゲル分率60〜98%の架橋発泡エチレン系重合体シートを雌雄一対の金型の間に挿入し加圧加熱して型物を成形する方法(特開昭55−55834号公報)、(3)架橋ポリエチレン系連続気泡体シートを90℃〜120℃に加熱し、常温の型で圧縮し、所望の形状に成形する方法(特開平9−48035号公報)等が提案されている。
【0003】
【発明が解決しようとする課題】
しかしながら、上記いずれの方法でも、加熱成型時に連続気泡が押しつぶされ、連続気泡独特の柔らかい風合いが無くなっていた。また、熱圧成形は、加熱冷却を繰り返す設備が必要であり、成形時間も長時間必要であった。従って、本発明の目的は、前記従来技術の欠点を解消し、簡単な設備による短時間の成形で、成形後も柔らかい風合いを保持する、連続気泡発泡体の成形方法を提供することにある。
【0004】
【課題を解決するための手段】
本発明によれば、前記目的を達成するために、本発明の連続気泡体の成形方法は、凹部を有する成形型の内面に沿って、連続気泡体シートを収納し、収納された発泡体の開口部に、輪状の固定部材を接着せしめることを特徴とする連続気泡発泡体の成形方法である。
【0005】
本発明において、連続気泡発泡体の基材は、ポリウレタン、ポリエチレン、エチレンー酢酸ビニル共重合体等のポリオレフィン等のフォームが柔軟性を有する材質であれば特に限定されないが、柔軟性、肌触りの面でEPDM連続気泡発泡体が好ましい。
【0006】
本発明の連続気泡発泡体は、発泡倍率10〜40倍のものが好ましい。発泡倍率が10倍未満であると、成形加工時に金型に押し込みむことができない。発泡倍率が40倍を超えると、柔らかすぎ、目的とする形状を得られない。
【0007】
本発明において、成形型の凹部の形状は特に限定されないが、略半球状が、成形上及び果物等の収納上好ましい。
【0008】
本発明において、連続気泡体の形状は最終成形品の形状によって適宜選択されるが、略円状のシートを、略半球状の凹部に収納することが、成形上好ましい。
【0009】
【発明の実施の形態】
本発明で使用される連続気泡体の製造方法としては、例えば、(1)ゴム類と軟化剤、充填剤、補強剤及び硫黄粉、加硫促進剤、加硫助剤、発泡剤、発泡助剤等からなるゴム組成物を混練機で混練し、押出機にてシート状に成形した未加硫シートを、金型枠内で圧縮成形し加熱を施し、ゴム生地を加圧、加熱し、実質上1部スコーチ状態とし、薄い表皮以外のゴム生地全体に極微小の発泡核を形成させる1次加熱段階の予備処理を施した後、次いで前記金型枠より取り出し、別途発泡倍率に合わせた大型の金型枠内で、発泡ならびに加硫を施す処理工程の2次加熱段階により製造する方法、(2)必要に応じて無機充填剤が添加されたポリオレフィン系樹脂に、熱分解型発泡剤の他、必要に応じて架橋剤、発泡助剤等を添加し、熱分解型発泡剤が実質的に分解しない温度で溶融混練し、所定形状に成形した後、加熱して架橋発泡させ、得られた架橋発泡体に機械的変形を加えて気泡を連通させ、その後、さらに連通孔を拡大させる方法が挙げられる。
【0010】
本発明において、ゴム類としては、エチレンプロピレンジエン共重合体ゴム(EPDM)、クロロプレンゴム、スチレンブタジエン共重合体ゴム等が好適に用いられる。
【0011】
本発明において軟化剤としては、パラフィン系プロセスオイル、ナフテン系プロセスオイル等のプロセスオイル、流動パラフィン等のパラフィン、その他ワセリン、ポリブテン、液状ポリブチレン等を用いることができる。
【0012】
本発明において、充填剤としては、例えば、炭酸カルシウム、タルクのほか、ゴム用ハードクレー等が好適に用いられる。
【0013】
本発明において、発泡剤として、例えばアゾジカルボンアミド、ジアゾアミノベンゼン等の如きアゾ化合物を主成分とし、これに別の発泡剤成分及び必要に応じてその他の配合剤を添加混合し、加熱分解温度の低下を図った発泡剤、その他ニトロソ化合物、スルホニル・ヒドラジド系等が用いられる。これらは単独で使用しても2種以上併用してもよい。
【0014】
本発明において、架橋剤としては、特には限定されず、従来公知の任意のものが使用されてよく、例えば、ジクミルパーオキサイド、1,1−ビス(t−ブチルパーオキシ)3,3,5−トリメチルシクロヘキサン、ジーt−ブチルパーオキシサイド,2,5−ジメチルー2,5−ジ(t−ブチルパーオキシ)ヘキセンー3等の有機過酸化物が挙げられ、これらは単独で使用しても2種以上併用しても良い。
【0015】
上記架橋剤を添加せず、上記ポリオレフィン系樹脂にシラン化合物をグラフトし、ポリオレフィン系樹脂を予め架橋性のものにしてもよい。シラン化合物としては、特に限定されず、従来公知の任意のもが使用されてよく、例えば、ビニルトリメトキシシラン、ビニルトリエトキシシラン、ビニルジメトキシシラン、3−メタクリロキシプロピルトリキシシラン等が挙げられる。
【0016】
さらに、電離性放射線照射により架橋を施してもよい。電離性放射線としては、例えば、電子線、α線、β線、γ線等が挙げられ、その照射量は適宜調整してもよい。
【0017】
本発明において発泡助剤としては、特には限定されず、従来公知の任意のものが使用されてよく、例えば、酸化亜鉛、尿素又はその誘導体、ステアリン酸マグネシウム、ステアリン酸亜鉛等が挙げられ、これらは単独で使用しても2種以上併用してもよい。発泡助剤は上記熱分解型発泡剤の分解温度、分解速度等を調整するものであり、その添加量は、製造条件や発泡剤量等に応じて適宜調整される。
【0018】
本発明の成形に当っては、上記連続気泡体を、好ましくは5〜40mmの厚みにスライスする。厚みが40mmを超えると、成形しにくく、5mm未満になると、成形品のクッション性が不足する。次ぎに、スライスした連続気泡体のシートを、凹部を有する成形型の内面に沿う様に収納する。該成形型の凹部は、成形品が所望とする形状を有し、略半球状を有することが好ましい。この場合、連続気泡体シートは、略円形であって、その直径は、成形型の開口部の直径の1.1倍〜2.0倍が好ましい。
【0019】
次ぎに、収納された発泡体の開口部に、輪状の固定部材を接着せしめる。該固定部材の材質は、特に限定されず、連続気泡体の広がる力を止めることの強度を有する材料であれば良く、例えば、発泡倍率5〜30倍のポリオレフィン発泡体、厚紙、樹脂成形品等が使用できる。
【0020】
上記固定部材を、連続気泡体シートの開口部に接着する方法としては、接着剤、熱融着、粘着等の方法が採用され、粘着による方法が最も簡便である。
【0021】
以下、本発明を図に従って具体的に説明する。図1は、略円状の連続気泡体シート1と略半球状の凹部2を有する成形型3を示している。図2は、連続気泡体シート1を成形型3の凹部2の内面に沿って収納しつつある概略図である。図3は、輪状の固定部材4を、成形型3の凹部2内に収納された連続気泡体シート1の開口部6に接着する前の概略図であって、固定部材4の下面には粘着加工5が施されている。図4は、固定部材4が、成形型3の凹部2内に収納された連続気泡体シート1の開口部6に接着された状態の概略図である。図5は、最終成形品7を、成形型3から離型した概略図である。図6は、本発明の成形方法により得られる成形品7に果物8を収納した利用例の概略図である。
【0022】
【実施例】
以下、実施例を示して本発明を更に具体的に説明するが、本発明は下記実施例により何等限定されるものではない。
【0023】
実施例1
EPDM連続気泡発泡体(商品名:オプシーラーOP−130、発泡倍率13倍、三和化工株式会社製)直径210mm、厚み10mmの円形シートを、直径150mm、深さ75mmの半球型の凹部を有する成形用型(金属製)の内面に沿う様に収納し、成形用型の上面に固定部材としてポリエチレン独立気泡発泡体(発泡倍率14倍)から成る輪状の芯材(外周の直径150mm、内周の直径130mm、厚み2mm)をアクリル系の粘着剤で貼り付けて、連続気泡発泡体の形状を固定し、成形用型から取り出した。
【0024】
成形後の連続気泡発泡体は、半球状の型の形状を保持し、気泡が押しつぶされず、柔らかい風合いを保ったものであり、クッション性があり、果物の収納袋として好適であった。
【0025】
実施例2
実施例1において、EPDM連続気泡体の替わりに、ポリエチレン系連続気泡体(商品名:オプセルLC−300#1、発泡倍率30倍、三和化工株式会社製)を使用した以外は、実施例1と同じ方法で成形した。得られた成形品は、半球状の型の形状を保持し、気泡が押しつぶされず、柔らかい風合いを保ったものであり、クッション性があり、果物の収納袋として好適であった。
【0026】
実施例3
実施例1において、固定部材を厚紙(外径、内径同じ)に替えた以外は、実施例1と同じ方法で成形品を得た。得られた半球状の型の形状を保持し、気泡が押しつぶされず、柔らかい風合いを保ったものであり、クッション性があり、果物の収納袋として好適であった。
【0027】
比較例1
実施例1において、EPDM連続気泡体シートを成型用型の凹部の内面に沿う様に収納し、形を整えた後、直下で加熱し、形状を固定した。成形後の連続気泡発泡体は、半球状の形状を保持するものの、表面の気泡が熱によりつぶされ、柔軟性に劣るものであった。
【0028】
【発明の効果】
以上のように、本発明に係る連続気泡発泡体の成形方法は、加熱工程を経ずに所望の形状に成形する為、成形時間が短く、省エネルギーで、加熱・冷却設備を必要としない。本発明で得られる連続気泡発泡体成形品は、その表面に連続気泡が残っている為、柔軟性に優れ、果物、野菜等の保持材やクッション材等に有用である。
【図面の簡単な説明】
【図1】本発明の成形前の成形型と連続気泡体シートである。
【図2】本発明の成形工程における連続気泡体シートを成形型に収納しつつある状態の概略図である。
【図3】本発明の成形工程のおける固定部材を、連続気泡体シートの開口部に接着する前の概略図である。
【図4】本発明の成形工程における固定部材を連続気泡体シートの開口部に接着した状態の概略図である。
【図5】本発明の成形方法で得られる成形品を、成形型から離型した状態の概略図である。
【図6】本発明の成形方法で得られる成形品の利用例を示す概略図である。
【符号の説明】
1 連続気泡体シート
2 凹部
3 成形型
4 固定部材
5 粘着加工
6 連続気泡体シートの開口部
7 成形品
8 果物[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a method for forming an open-cell foam used for holding materials and cushion materials such as fruits and vegetables.
[0002]
[Prior art]
Conventionally, the foam is molded by heating by a method such as hot-pressure molding according to the target shape. For example, (1) while heating one or two or more pieces of a cross-linked foam of a polyolefin or a mixture of a polyolefin and a polymerizable rubber or plastic to a temperature above the softening point of the polyolefin in a mold A molding method (Japanese Patent Publication No. 52-49022) in which compression is performed at least 20% from one direction and then pressure is applied, and (2) a cross-linked foamed ethylene polymer sheet having a gel fraction of 60 to 98% is male and female. A method of forming a mold by inserting between a pair of molds and pressurizing and heating (Japanese Patent Application Laid-Open No. 55-55834), (3) heating a cross-linked polyethylene-based open cell sheet to 90 ° C. to 120 ° C. A method of compressing with a normal temperature mold and forming it into a desired shape (Japanese Patent Laid-Open No. 9-48035) has been proposed.
[0003]
[Problems to be solved by the invention]
However, in any of the above methods, the open cells were crushed during the heat molding, and the soft texture peculiar to open cells was lost. In addition, hot pressing requires equipment for repeated heating and cooling, and requires a long molding time. Accordingly, an object of the present invention is to provide a method for forming an open-cell foam that eliminates the disadvantages of the prior art and retains a soft texture even after molding by simple molding with a short period of time.
[0004]
[Means for Solving the Problems]
According to the present invention, in order to achieve the above-mentioned object, the method for molding an open cell body of the present invention is to store an open cell sheet along the inner surface of a mold having a recess, An open-cell foam molding method characterized by adhering a ring-shaped fixing member to an opening.
[0005]
In the present invention, the base material of the open-cell foam is not particularly limited as long as the foam such as polyurethane, polyethylene, and polyolefin such as ethylene-vinyl acetate copolymer has flexibility, but in terms of flexibility and touch. EPDM open cell foam is preferred.
[0006]
The open-cell foam of the present invention preferably has an expansion ratio of 10 to 40 times. If the expansion ratio is less than 10, it cannot be pushed into the mold during molding. When the expansion ratio exceeds 40 times, it is too soft and the desired shape cannot be obtained.
[0007]
In the present invention, the shape of the concave portion of the mold is not particularly limited, but a substantially hemispherical shape is preferable for molding and storage of fruits and the like.
[0008]
In the present invention, the shape of the open-cell body is appropriately selected depending on the shape of the final molded product, but it is preferable in terms of molding to store a substantially circular sheet in a substantially hemispherical recess.
[0009]
DETAILED DESCRIPTION OF THE INVENTION
Examples of the method for producing an open cell body used in the present invention include (1) rubbers and softeners, fillers, reinforcing agents and sulfur powder, vulcanization accelerators, vulcanization aids, foaming agents, foaming aids. A kneading machine is used to knead a rubber composition composed of an agent, etc., and an unvulcanized sheet molded into a sheet by an extruder is compression-molded in a mold frame and heated, and the rubber fabric is pressurized and heated. After a pre-treatment in the primary heating stage to form a very small foam core on the entire rubber fabric other than the thin skin, it was then removed from the mold frame and separately adjusted to the expansion ratio. A method of manufacturing by a secondary heating stage of a foaming and vulcanizing treatment process in a large mold frame, (2) a pyrolytic foaming agent to a polyolefin resin to which an inorganic filler is added if necessary In addition, if necessary, a crosslinking agent, a foaming aid, etc. are added, After melt-kneading at a temperature that does not qualitatively decompose and molding into a predetermined shape, it is heated to cross-link and foam, and the resulting cross-linked foam is mechanically deformed to allow bubbles to communicate, and then the communication hole is further expanded. The method of letting it be mentioned.
[0010]
In the present invention, as the rubbers, ethylene propylene diene copolymer rubber (EPDM), chloroprene rubber, styrene butadiene copolymer rubber and the like are preferably used.
[0011]
As the softening agent in the present invention, process oil such as paraffinic process oil and naphthenic process oil, paraffin such as liquid paraffin, petrolatum, polybutene, liquid polybutylene, and the like can be used.
[0012]
In the present invention, as the filler, for example, calcium carbonate, talc, and hard clay for rubber are preferably used.
[0013]
In the present invention, as a foaming agent, for example, an azo compound such as azodicarbonamide, diazoaminobenzene or the like is a main component, and another foaming agent component and other compounding agents are added to and mixed with this, and a thermal decomposition temperature is added. For example, a foaming agent, a nitroso compound, a sulfonyl hydrazide, or the like that is used for reducing the temperature of the resin is used. These may be used alone or in combination of two or more.
[0014]
In the present invention, the crosslinking agent is not particularly limited, and any conventionally known crosslinking agent may be used. For example, dicumyl peroxide, 1,1-bis (t-butylperoxy) 3, 3, Examples include organic peroxides such as 5-trimethylcyclohexane, di-t-butylperoxyside, 2,5-dimethyl-2,5-di (t-butylperoxy) hexene-3, and these may be used alone. Two or more kinds may be used in combination.
[0015]
A silane compound may be grafted to the polyolefin resin without adding the crosslinking agent, and the polyolefin resin may be previously crosslinkable. The silane compound is not particularly limited, and any conventionally known silane compound may be used. Examples thereof include vinyltrimethoxysilane, vinyltriethoxysilane, vinyldimethoxysilane, and 3-methacryloxypropyltrixysilane. .
[0016]
Further, crosslinking may be performed by ionizing radiation irradiation. Examples of the ionizing radiation include electron beams, α rays, β rays, γ rays, and the dose may be appropriately adjusted.
[0017]
In the present invention, the foaming aid is not particularly limited, and any conventionally known one may be used. Examples thereof include zinc oxide, urea or a derivative thereof, magnesium stearate, zinc stearate, and the like. May be used alone or in combination of two or more. The foaming assistant adjusts the decomposition temperature, decomposition rate, and the like of the above pyrolyzable foaming agent, and the amount added is appropriately adjusted according to the production conditions, the amount of foaming agent, and the like.
[0018]
In the molding of the present invention, the open cell body is preferably sliced to a thickness of 5 to 40 mm. When the thickness exceeds 40 mm, molding is difficult, and when the thickness is less than 5 mm, the cushioning property of the molded product is insufficient. Next, the sheet | seat of the sliced open cell body is accommodated along the inner surface of the shaping | molding die which has a recessed part. The concave portion of the mold has a shape desired by the molded product, and preferably has a substantially hemispherical shape. In this case, the open cell sheet is substantially circular, and its diameter is preferably 1.1 to 2.0 times the diameter of the opening of the mold.
[0019]
Next, a ring-shaped fixing member is bonded to the opening of the accommodated foam. The material of the fixing member is not particularly limited as long as it is a material having the strength of stopping the spreading force of open cells, for example, a polyolefin foam having a foaming ratio of 5 to 30 times, a cardboard, a resin molded product, etc. Can be used.
[0020]
As a method of adhering the fixing member to the opening of the open cell sheet, methods such as an adhesive, heat fusion, and adhesion are adopted, and the method using adhesion is the simplest.
[0021]
Hereinafter, the present invention will be specifically described with reference to the drawings. FIG. 1 shows a
[0022]
【Example】
EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not limited to the following examples.
[0023]
Example 1
EPDM open cell foam (trade name: Opsealer OP-130, expansion ratio 13 times, manufactured by Sanwa Kako Co., Ltd.) Molding a circular sheet with a diameter of 210 mm and a thickness of 10 mm with a hemispherical recess having a diameter of 150 mm and a depth of 75 mm It is housed along the inner surface of the mold (made of metal), and a ring-shaped core material (outer diameter 150 mm, inner diameter) made of polyethylene closed cell foam (expanding ratio 14 times) as a fixing member on the upper surface of the molding mold The diameter of 130 mm in diameter and 2 mm in thickness) was pasted with an acrylic pressure-sensitive adhesive to fix the shape of the open-cell foamed material and taken out from the molding die.
[0024]
The open-cell foam after molding maintained the shape of a hemispherical mold, the bubbles were not crushed, kept a soft texture, had cushioning properties, and was suitable as a fruit storage bag.
[0025]
Example 2
In Example 1, Example 1 was used except that a polyethylene-based open cell (trade name: Opcell LC-300 # 1, foaming ratio 30 times, manufactured by Sanwa Chemical Co., Ltd.) was used instead of the EPDM open cell. The same method was used. The obtained molded article retained the shape of a hemispherical mold, did not crush bubbles, maintained a soft texture, had cushioning properties, and was suitable as a fruit storage bag.
[0026]
Example 3
In Example 1, a molded product was obtained in the same manner as in Example 1 except that the fixing member was changed to cardboard (the same outer diameter and inner diameter). The shape of the obtained hemispherical mold was maintained, bubbles were not crushed, a soft texture was maintained, cushioning properties, and suitable as a fruit storage bag.
[0027]
Comparative Example 1
In Example 1, the EPDM open cell sheet was stored so as to be along the inner surface of the concave portion of the molding die, and after adjusting the shape, it was heated immediately below to fix the shape. Although the open-cell foam after molding maintains a hemispherical shape, the bubbles on the surface are crushed by heat and the flexibility is poor.
[0028]
【The invention's effect】
As described above, the method for forming an open-cell foam according to the present invention is formed into a desired shape without going through a heating step. Therefore, the forming time is short, energy is saved, and heating / cooling equipment is not required. The open-cell foamed molded article obtained by the present invention has excellent flexibility because it has open cells on its surface, and is useful for holding materials such as fruits and vegetables, cushioning materials, and the like.
[Brief description of the drawings]
FIG. 1 shows a molding die and an open cell sheet before molding according to the present invention.
FIG. 2 is a schematic view of a state in which an open cell sheet is being stored in a mold in the molding process of the present invention.
FIG. 3 is a schematic view before the fixing member in the molding step of the present invention is bonded to the opening of the open cell sheet.
FIG. 4 is a schematic view of a state in which a fixing member is bonded to an opening of an open cell sheet in the molding process of the present invention.
FIG. 5 is a schematic view showing a state where a molded product obtained by the molding method of the present invention is released from a mold.
FIG. 6 is a schematic view showing an example of use of a molded product obtained by the molding method of the present invention.
[Explanation of symbols]
DESCRIPTION OF SYMBOLS 1 Open cell sheet 2 Recessed
Claims (4)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002128937A JP4166502B2 (en) | 2002-04-30 | 2002-04-30 | Molding method of open cell foam |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002128937A JP4166502B2 (en) | 2002-04-30 | 2002-04-30 | Molding method of open cell foam |
Publications (2)
| Publication Number | Publication Date |
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| JP2003320579A JP2003320579A (en) | 2003-11-11 |
| JP4166502B2 true JP4166502B2 (en) | 2008-10-15 |
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| JP2002128937A Expired - Fee Related JP4166502B2 (en) | 2002-04-30 | 2002-04-30 | Molding method of open cell foam |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS54146675U (en) * | 1977-12-15 | 1979-10-12 | ||
| JPS624071A (en) * | 1985-06-17 | 1987-01-10 | 東洋アルミホイルプロダクツ株式会社 | Package and manufacture thereof |
| JPH0631108B2 (en) * | 1988-05-30 | 1994-04-27 | 株式会社池口工業 | Foam synthetic resin packaging |
| JPH0259176U (en) * | 1988-10-26 | 1990-04-27 | ||
| JPH068274A (en) * | 1992-06-24 | 1994-01-18 | Ono Sangyo Kk | Production of bag-form article integrally provided with ring on its open end |
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