JPH1134174A - Production of anisotropic styrenic resin foam - Google Patents
Production of anisotropic styrenic resin foamInfo
- Publication number
- JPH1134174A JPH1134174A JP9193636A JP19363697A JPH1134174A JP H1134174 A JPH1134174 A JP H1134174A JP 9193636 A JP9193636 A JP 9193636A JP 19363697 A JP19363697 A JP 19363697A JP H1134174 A JPH1134174 A JP H1134174A
- Authority
- JP
- Japan
- Prior art keywords
- foam
- compression
- thickness
- resin foam
- anisotropic
- 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 96
- 238000004519 manufacturing process Methods 0.000 title claims description 16
- 229920001890 Novodur Polymers 0.000 title abstract description 7
- 238000007906 compression Methods 0.000 claims abstract description 86
- 230000006835 compression Effects 0.000 claims abstract description 83
- 238000000034 method Methods 0.000 claims abstract description 25
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 58
- 239000011148 porous material Substances 0.000 claims description 24
- 229920005989 resin Polymers 0.000 claims description 22
- 239000011347 resin Substances 0.000 claims description 22
- 238000012545 processing Methods 0.000 claims description 18
- 239000002184 metal Substances 0.000 abstract description 3
- 229910052751 metal Inorganic materials 0.000 abstract description 3
- 150000002739 metals Chemical class 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 10
- 230000006837 decompression Effects 0.000 description 10
- 239000004794 expanded polystyrene Substances 0.000 description 9
- 210000004027 cell Anatomy 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- 239000000178 monomer Substances 0.000 description 4
- 239000012466 permeate Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000005336 cracking Methods 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000000047 product Substances 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
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 210000002421 cell wall Anatomy 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000002093 peripheral effect Effects 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 229920006380 polyphenylene oxide Polymers 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 210000000497 foam cell Anatomy 0.000 description 1
- 238000010097 foam moulding Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920000573 polyethylene Polymers 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
- 238000012805 post-processing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は実質的に等方性のス
チレン系発泡体を圧縮処理することにより測定方向によ
って機械的、物理的性状が異なる性質を示す異方性スチ
レン系樹脂発泡体の製造法に関する。BACKGROUND OF THE INVENTION The present invention relates to an anisotropic styrene-based resin foam which exhibits substantially different mechanical and physical properties depending on the measurement direction by compressing a substantially isotropic styrene-based foam. Related to manufacturing method.
【0002】[0002]
【従来の技術】高分子発泡体は多くの気泡体から構成さ
れることに基づく断熱性,衝撃吸収性,単位重量あたり
の曲げ剛性などに優れ多くの分野に使われている。代表
的な発泡体は発泡ポリスチレン(EPS),発泡ポリエ
チレン(EPE),発泡ポリプロピレン(EPP)、発
泡ポリウレタン(EPU)などである.スチレン系樹脂
発泡体の一つであるEPSはEPE,軟質EPUに比べ
同じ密度で剛性が高いが柔軟性は小さく,また荷重によ
る変形・歪にが復元しにくい。EPE,軟質EPUはE
PSに比べ,柔軟性,変形の復元性で優れるが,硬さ,
剛性面で劣る。2. Description of the Related Art Polymer foams are used in many fields because of their excellent heat insulating properties, shock absorption properties, bending stiffness per unit weight, etc., which are composed of many foams. Typical foams are expanded polystyrene (EPS), expanded polyethylene (EPE), expanded polypropylene (EPP), expanded polyurethane (EPU), and the like. EPS, which is one of the styrene-based resin foams, has the same density and high rigidity as EPE and soft EPU, but has low flexibility, and hardly recovers from deformation and strain due to load. EPE, soft EPU is E
Compared with PS, it is superior in flexibility and restoring property of deformation.
Poor in rigidity.
【0003】独立気泡の硬質発泡シートに圧縮力を加え
ることで柔軟性が付与されることは知られている(英国
特許911,995号明細書,米国特許3,159,7
00号明細書)。特開平7−148761号公報には周
知慣用の発泡板体を圧縮による後処理に付して、10M
N/m3あるいはそれ以下の動的剛性率を示す発泡板体
を製造する方法であって、見かけ比重17〜30kg/
m3の発泡板体を、その当初の60〜90%の最大圧縮
歪み率となるまで圧縮して圧縮永久歪み率を高め、この
処理を少なくとも1回反復することを特徴とする方法が
示されているが、圧縮処理回数は5回から10回と工程
数が多いこと、板体厚さに制約があるなどの課題が残さ
れている。また、スチレン系樹脂の発泡体を型枠内に入
れて圧縮歪みが25〜50%となるように圧縮すること
により高弾性の発泡スチレン系樹脂を得る方法は特開昭
56−51337号公報に記載されている。この方法で
も所定の圧縮率まで到達するのに複数回の圧縮操作を要
する。複数回の圧縮操作をしないときは発泡体の変形や
亀裂を生じてしまう。[0003] It is known that flexibility is imparted by applying a compressive force to a closed-cell hard foam sheet (GB Patent 911,995, US Patent 3,159,7).
00 specification). Japanese Patent Application Laid-Open No. 7-148761 discloses that a well-known and commonly used foamed plate is subjected to post-processing by compression to obtain a 10M
A method for producing a foamed plate having a dynamic rigidity of N / m 3 or less, comprising an apparent specific gravity of 17 to 30 kg /
The foam board body m 3, the compression until the original 60% to 90% maximum compression strain rate of increasing the compression set ratio, wherein the repeating at least once the process is shown However, there remain problems such as the number of steps of the compression processing being as many as 5 to 10 times and the thickness of the plate being limited. Japanese Patent Application Laid-Open No. 56-51337 discloses a method for obtaining a highly elastic foamed styrene resin by placing a foam of a styrene resin in a mold and compressing the foam so that the compression strain is 25 to 50%. Are listed. This method also requires a plurality of compression operations to reach a predetermined compression ratio. If the compression operation is not performed a plurality of times, the foam may be deformed or cracked.
【0004】一方、特開平2−299321号公報には
「独立気泡構造の熱可塑性樹脂発泡成形体を減圧室に入
れ、減圧に晒した後圧縮する方法を提案されているが次
のような問題が残されている。(1)カサ高い発泡体を
収容し減圧状態に耐える高強度の減圧室が必要。(2)
減圧処理の工程が増え全体としては処理時間が長くなり
かねない。(3)減圧室から大気圧中に取り出された発
泡体は時間の経過と共に減圧状態が変化しこのため次の
工程との関係で品質の安定性に問題が生じる。(4)発
泡体が大きくなると相対的に表面積が減少するため減圧
処理が内部に及ぶのに長い時間を要し結果として生産性
が低下する。このように公知の方法は発泡体の変形、亀
裂などの製品品質と処理時間、工数が矛盾関係にあっ
た。On the other hand, Japanese Patent Application Laid-Open No. Hei 2-299321 proposes a method in which a foamed thermoplastic resin article having a closed cell structure is placed in a decompression chamber, exposed to reduced pressure and then compressed. (1) A high-strength decompression chamber for accommodating bulky foam and enduring decompression is required.
The number of steps of the decompression treatment increases, and the treatment time may become longer as a whole. (3) The foam taken out from the decompression chamber into the atmospheric pressure changes its decompression state with the passage of time, which causes a problem in quality stability in relation to the next step. (4) As the foam becomes larger, the surface area relatively decreases, so that it takes a long time for the decompression treatment to reach inside, and as a result, the productivity is reduced. As described above, in the known methods, there is a contradictory relationship between the product quality such as deformation and cracking of the foam and the processing time and man-hour.
【0005】発泡体は圧縮されることにより構成する気
泡体が変形を起こしつつ体積を減少する。この際、気泡
内部の圧力は増し、気体は外に向かって透過、逸散しよ
うとするが、発泡体外部に到達するまでには無数とも言
える気泡壁を透過せねばならない。このため圧縮処理の
速度がこの気体の逸散の速度より大きいときには発泡体
内部の圧力が異常に高まり、圧縮力を解除したあとに残
存した圧力が発泡体を変形させたり、ときに発泡体に亀
裂を生じさせたりすることになる。この傾向は気泡内部
の気体が圧力の小さい発泡体外部に透過、逸散する距離
が長い場合に起こりやすい。すなわち、発泡体が厚くて
広い面積のものほどこの傾向が大きい。[0005] The volume of the foam is reduced while the foam formed by the compression is deformed. At this time, the pressure inside the cells increases, and the gas tries to permeate and escape outward, but must pass through the myriad of cell walls before reaching the outside of the foam. For this reason, when the speed of the compression process is higher than the speed of the gas escape, the pressure inside the foam increases abnormally, and the pressure remaining after the compression force is released deforms the foam, and sometimes the foam is deformed. Or cracks. This tendency is likely to occur when the gas inside the cells has a long distance to permeate and escape to the outside of the foam having a small pressure. In other words, this tendency is greater as the foam is thicker and has a larger area.
【0006】この現象をより詳細に観察してみると、発
泡体が圧縮荷重を受けると荷重を受けた部分の発泡体が
変形しこれを構成する気泡の圧力が増加し、この発泡体
外部との圧力差が推進力となって気体は気泡体外部に透
過/逸散するが、実際は初めに発泡体外部に接する部分
の気泡から気泡壁を通して外部に透過/逸散が起こり、
その気泡の圧力が低下し、その気泡の隣の気泡との間に
圧力差が生じそれが推進力になり、気泡壁を通して透過
/逸散が起こるというように内部に伝搬していくことに
なる。硬質発泡体の物理特性が変わることの最大要因は
その気泡が断面上で扁平構造になることであると推察さ
れる。本発明者らの実験、観察によればこの気泡の扁平
化は圧縮荷重を受けた発泡体の気泡全部に同時に起こる
のではなく、外部または圧力の低い空間に接した部分か
ら生じ、このことから前述の透過/逸散の仮説が確認さ
れた。When this phenomenon is observed in more detail, when the foam is subjected to a compressive load, the foam in the load-receiving portion is deformed, and the pressure of the cells constituting the foam is increased. The pressure difference becomes the driving force, and the gas permeates / dissipates outside the foam. However, in actuality, the permeation / dissipation occurs first from the bubbles in contact with the outside of the foam through the cell wall.
The pressure of the bubble is reduced, and a pressure difference is generated between the bubble and the bubble next to the bubble, which becomes a driving force, and propagates inside such that transmission / dissipation occurs through the bubble wall. . It is presumed that the biggest factor in changing the physical properties of the rigid foam is that the cells have a flat structure in cross section. According to the experiments and observations of the present inventors, the flattening of the bubbles does not occur simultaneously with all the bubbles of the foam subjected to the compression load, but occurs from a portion in contact with the outside or a low pressure space. The aforementioned transmission / dissipation hypothesis was confirmed.
【0007】[0007]
【発明が解決しようとする課題】本発明は上記のような
異方性発泡体の生産過程での処理時間、工数の多さの問
題を解決しスチレン系発泡体から品質に優れた異方性ス
チレン樹脂発泡体の製造法を提供するものである。請求
項1は異方性スチレン系樹脂発泡体の製造法を基本概念
を提供する。請求項2は変形、亀裂などのない異方性ス
チレン系樹脂発泡体の製造法を提供する。請求項3は変
形、亀裂などのない異方性スチレン系樹脂発泡体の効率
のよい製造法を提供する。請求項4は異方性発泡体の短
時間の製造法を提供する。請求項5は生産性、品質で効
果を発揮する製造法を提供する。SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems of processing time and man-hours in the production process of anisotropic foams, and provides anisotropic foams of excellent quality from styrene-based foams. A method for producing a styrene resin foam is provided. Claim 1 provides a basic concept of a method for producing an anisotropic styrenic resin foam. Claim 2 provides a method for producing an anisotropic styrenic resin foam without deformation, cracking, and the like. Claim 3 provides an efficient method for producing an anisotropic styrenic resin foam without deformation or cracking. Claim 4 provides a short time method for producing an anisotropic foam. Claim 5 provides a production method that is effective in productivity and quality.
【0008】[0008]
【課題を解決するための手段】本発明はスチレン系樹脂
発泡体に複数の気孔を設け次いで発泡体を圧縮する異方
性スチレン系樹脂発泡体の製造法に関する。本発明にお
いては、密度が7〜50kg/m3のスチレン系樹脂発
泡体に断面積が0.5〜10mm2の複数の気孔を設け
次いで発泡体の初期の厚さの60〜5%となるまで圧縮
し、圧縮終了後の厚さが初期厚さに対し90〜10%と
なるように圧縮することが好ましい。本発明において
は、圧縮工程中に、圧縮面を減圧吸引することが好まし
い。SUMMARY OF THE INVENTION The present invention relates to a method for producing an anisotropic styrene resin foam in which a plurality of pores are provided in a styrene resin foam and the foam is then compressed. In the present invention, a styrene resin foam having a density of 7 to 50 kg / m 3 is provided with a plurality of pores having a cross-sectional area of 0.5 to 10 mm 2 , and then has a thickness of 60 to 5% of the initial thickness of the foam. It is preferable to compress so that the thickness after the compression is 90 to 10% of the initial thickness. In the present invention, it is preferable that the compressed surface is suctioned under reduced pressure during the compression step.
【0009】本発明においては、圧縮前のスチレン系発
泡体の圧縮方向の厚さが3cm以上で体積が4000c
m3以上の発泡体であることが好ましい。本発明におい
ては、圧縮処理時の圧縮率((圧縮処理前の寸法−圧縮
処理後の寸法)/圧縮処理前の寸法)×100%を70
%以上とすることが好ましい。In the present invention, the thickness of the styrene foam before compression is 3 cm or more in the compression direction and the volume is 4000 c.
It is preferably a foam of m 3 or more. In the present invention, the compression ratio at the time of compression processing ((dimension before compression processing−dimension after compression processing) / dimension before compression processing) × 100% is calculated as 70%.
% Is preferable.
【0010】[0010]
【発明の実施の形態】スチレン系樹脂発泡体とは,スチ
レンの重合体の発泡体の他、スチレンを主成分として他
のモノマーと共重合したものあるいはスチレン樹脂を主
体としてスチレン以外の重合体との混合物の発泡体をも
指す。他のモノマー成分としてはスチレンと共重合しう
るモノマー例えばブタジエン、アクリロニトリル、アク
リル酸エステル類、ジビニルベンゼン、ブロム化スチレ
ン、マレイン酸などである。スチレン樹脂と混合物とな
りうる重合体としては前記スチレンと共重合しうるモノ
マーの単独または共重合体、ポリエチレン、ポリフェニ
レンオキサイド(PPO)などがある。DESCRIPTION OF THE PREFERRED EMBODIMENTS A styrene-based resin foam refers to a foam of styrene polymer, a copolymer of styrene as a main component with other monomers, or a polymer of styrene resin as a main component other than styrene. Also refers to a foam of a mixture of Other monomer components include monomers copolymerizable with styrene, such as butadiene, acrylonitrile, acrylates, divinylbenzene, brominated styrene, and maleic acid. Examples of the polymer that can be a mixture with the styrene resin include a homopolymer or a copolymer of the above-mentioned monomer copolymerizable with styrene, polyethylene, and polyphenylene oxide (PPO).
【0011】スチレン系樹脂を発泡体とする方法として
は押出機を用いて押し出しと同時に発泡するもの、発泡
性を付与した粒状樹脂を加熱し、次いでこの発泡粒を型
に込めて再度加熱し成形するものなどがあるが本発明は
後者の粒状物から発泡成形する方法によるものが好まし
い。発泡体の形態上の特別な制約はないが本発明で特に
効果を現すのは圧縮方向の寸法(厚さ)と1回の処理時
の体積が大きいものである。このような物ほど変形や、
割れがなどの品質上の問題が起こりやすく一方、生産性
も低いからである。具体的には圧縮前の発泡体の圧縮方
向の厚さが3cm以上で全体積が4000cm3以上の
ものが好ましい。As a method of forming a styrene-based resin into a foam, an extruder is used to extrude and foam simultaneously with extruding. A foamed resin is heated, and then the foamed granules are put into a mold and heated again to mold. However, the present invention preferably employs the latter method of foam molding from granular material. Although there is no particular restriction on the form of the foam, what is particularly effective in the present invention is that the size (thickness) in the compression direction and the volume in one processing are large. Such a thing deforms,
This is because quality problems such as cracks are likely to occur, while productivity is low. The thickness of the concrete in the compression direction of the foam before compression is the total volume in 3cm or preferably from 4000 cm 3 or more.
【0012】用いられる発泡体の密度としては7〜50
kg/m3が好ましい。7kg/m3未満であれば発泡体
の形状が不安定となる傾向があり、一方、50kg/m
3を越えると材質的に弾力性を有するゴム、エラストマ
ーなどの発泡体と比較してその特長が小さくなる傾向が
ある。The density of the foam used is 7 to 50.
kg / m 3 is preferred. If it is less than 7 kg / m 3 , the shape of the foam tends to be unstable, while 50 kg / m 3
If it exceeds 3 , its characteristics tend to be smaller than foams such as rubber and elastomer which have elasticity in material.
【0013】気孔は発泡体の内部まで到達しかつ、孔の
一端が外部に通じるように設けられる。気孔の深さ方向
の角度など特別の制約はないが、通常、圧縮面に対して
垂直に片側または両側に通じるように設けられる。気孔
の形状には制約はない。気孔の機能は圧力が高まった気
泡体内部の気体に逃げ道を与えることであり、その効果
は圧縮工程で発泡体の体積が減少する際の内圧上昇を緩
和することである。作業性の観点から通常、断面が円形
状の錐が用いられる。気孔は気泡壁を通して逸散してく
る気体の通り道なので小さなものでも効果は大きい。た
だ、加工上の効率性から断面積で0.5mm2以上が好
ましい。一方、大きすぎると発泡体の機械特性などに影
響を与えるので10mm2以下が好ましい。The pores are provided so as to reach the inside of the foam and one end of the pores communicates with the outside. Although there is no particular restriction such as the angle in the depth direction of the pores, it is usually provided so as to communicate with one or both sides perpendicularly to the compression surface. There are no restrictions on the shape of the pores. The function of the pores is to provide an escape path for the gas inside the foam with increased pressure, and its effect is to alleviate the increase in internal pressure when the volume of the foam is reduced in the compression step. Usually, a cone having a circular cross section is used from the viewpoint of workability. Since the pores are the passages of the gas that escapes through the bubble wall, even small ones are effective. However, in terms of processing efficiency, the cross-sectional area is preferably 0.5 mm 2 or more. On the other hand, preferably 10 mm 2 or less because influence such as mechanical properties of the foam too large.
【0014】気孔の設置面は圧縮面を主体にするが補助
的に圧縮面と垂直な面にも設けてもよい。気孔の設置方
向または角度に制約はないが加工上発泡体面に垂直な方
向が好ましい。The surface on which the pores are provided is mainly a compression surface, but may be additionally provided on a surface perpendicular to the compression surface. There is no restriction on the direction or angle of the pores, but a direction perpendicular to the foam surface is preferred for processing.
【0015】気孔の数は発泡体の厚さ、全体積、密度、
目的とする圧縮度などを考慮する必要があるが、本発明
を効果的に実施するには物理特性上100cm2当たり
およそ2個から400個の範囲とされることが好まし
い。圧縮面の周辺部は少なく、中心部は多くするなどの
工夫は有効である。The number of pores depends on the thickness, total volume, density,
Although it is necessary to take into account the desired degree of compression and the like, in order to effectively carry out the present invention, the range is preferably about 2 to 400 per 100 cm 2 in terms of physical characteristics. It is effective to reduce the peripheral portion of the compression surface and increase the central portion.
【0016】気孔を設ける方法に制約はないが、例えば
対象となる発泡体が準備できているときには、針または
錐状のジグで刺し貫くように設ける方法があり、発泡粒
を型に込めてスチームなどで加熱成形して発泡体を製造
する場合は針金状のものを型内に設けておき成形が完了
後これらを引き抜く方法などがある。There is no particular limitation on the method of forming the pores. For example, when the target foam is ready, there is a method of piercing with a needle or a conical jig. In the case of producing a foam by heat molding with a method such as, for example, there is a method in which a wire is provided in a mold, and after molding is completed, these are pulled out.
【0017】圧縮処理量は目的とする発泡体製品の物理
特性を考慮して選ばれる。一般的には圧縮処理量が大き
くなるほど圧縮率は大きくなるが、発泡体の密度、気泡
構造、圧縮速度、圧縮保持時間などによって影響を受け
る。本発明の効果が大きく表れる30%以上の圧縮率も
のを得るためは、発泡体の初期の厚さの60〜5%の範
囲とされることが好ましい。The amount of compression treatment is selected in consideration of the physical properties of the target foam product. In general, the compression ratio increases as the compression processing amount increases, but it is affected by the density of the foam, the cell structure, the compression speed, the compression holding time, and the like. In order to obtain a compression ratio of 30% or more at which the effect of the present invention is greatly exhibited, the thickness is preferably in the range of 60 to 5% of the initial thickness of the foam.
【0018】圧縮は通常は平行な2枚の金属などの剛体
(以後圧縮盤という)間に発泡体を置いて剛体の間隔を
油圧力など狭めて行う。その速度および所定の圧縮量ま
で達したときの圧縮盤の保持時間は発泡体の気泡から気
体が透過/逸散する速度を考慮して決められる。本発明
においては圧縮速度は20〜100cm/分、保持時間
は1秒〜20分とすることが好ましい。圧縮盤の発泡体
に接する面は製品の特性、外観を損ねない程度の実質的
に平面であることが求められるが、かつ多孔質構造か3
00メッシュより粗い面か、碁盤の目の浅い溝などがあ
ってもよい。気孔から逸散してきた気体が逃げやすくす
るためである。The compression is usually performed by placing a foam between two parallel rigid bodies such as metal (hereinafter referred to as a compression platen) and reducing the distance between the rigid bodies by means of hydraulic pressure or the like. The speed and the holding time of the compression platen when reaching a predetermined compression amount are determined in consideration of the speed at which gas permeates / dissipates from the foam cells. In the present invention, the compression speed is preferably 20 to 100 cm / min, and the holding time is preferably 1 second to 20 minutes. The surface of the compression plate in contact with the foam is required to be substantially flat so as not to impair the properties and appearance of the product.
There may be a surface rougher than 00 mesh or a shallow groove on the grid. This is to make it easier for gas that has escaped from the pores to escape.
【0019】圧縮面を減圧に保持しつつ処理を行うこと
により、気孔からの気体の流出を促進する効果がある。
この際、圧縮面は多孔質の材料か気孔を持つ金属板で製
作される。この際、盤面の開口度は発泡体に設けた気孔
のそれより大きくなるようにする。減圧の程度は200
mmHg以上とすることが好ましく、真空ポンプの容量
は発泡体の体積などを勘案して決められる。By performing the treatment while maintaining the compression surface at a reduced pressure, there is an effect of promoting the outflow of gas from the pores.
At this time, the compression surface is made of a porous material or a metal plate having pores. At this time, the opening degree of the board is set to be larger than that of the pores provided in the foam. Decompression degree is 200
The pressure is preferably not less than mmHg, and the capacity of the vacuum pump is determined in consideration of the volume of the foam.
【0020】[0020]
【実施例】次に実施例により本発明をさらに詳細に説明
するが、本発明はこれらに制限されるものではない。Next, the present invention will be described in more detail by way of examples, but the present invention is not limited to these examples.
【0021】[実施例1〜4]発泡前の平均粒子径0.
8mmの発泡ポリスチレン(EPS:日立化成工業
(株)製ハイビーズSSB)を通常のEPSと同様、加
圧式予備発泡を行い、熟成後、融着成形法により成形し
た略寸法縦184cm横92cm厚さ41cmの発泡ポ
リスチレン(通称EPSブロック)を、充分乾燥したの
ち、周辺部を避けて、縦30cm横30cm厚さ18c
m、体積16200cm3の試験片を5個切り出しそれ
ぞれの密度を測定した。このうち3個の試験片には2.
5cm間隔で断面積3.14mm2 (直径2mm)の錐
で厚さ方向に121個の気孔を穿った。[Examples 1 to 4] The average particle diameter before foaming was 0.1.
8 mm expanded polystyrene (EPS: Hi-Beads SSB manufactured by Hitachi Chemical Co., Ltd.) was subjected to pressurized prefoaming in the same manner as ordinary EPS, and after aging, was molded by a fusion molding method. After fully drying the expanded polystyrene (commonly known as EPS block), avoiding the peripheral part, it is 30 cm long, 30 cm wide and 18 cm thick.
Five test pieces having a size of m and a volume of 16200 cm 3 were cut out and the respective densities were measured. Of these, three specimens had 2.
121 pores were drilled in the thickness direction with a cone having a sectional area of 3.14 mm 2 (diameter of 2 mm) at intervals of 5 cm.
【0022】圧縮処理は上昇時に盤間の距離が縮まり下
降するときに盤間が開くように作動する型締め力20ト
ンの油圧式圧縮装置を用いた。圧縮はいずれも350m
m/分で行った。For the compression processing, a hydraulic compression device with a mold clamping force of 20 tons that operates so as to reduce the distance between the boards when ascending and open the boards when descending. 350m compression
m / min.
【0023】この実験で圧縮量とはあらかじめ装置に設
定してある圧縮行程最後の盤間距離に対する処理前の厚
さの百分比を意味する。保持時間とは設定した盤間距離
まで圧縮盤が到達した時にその位置で保持する時間をい
う。圧縮率とは圧縮処理終了後24時間後の発泡体試験
片の厚みの元の厚みに対する百分比である。変形してい
るものも中央部の寸法を用いた。変形量とは試験片の4
片の中間部の厚さの平均と中央部の厚さの差を4片の厚
さの平均で除し100を乗じこれから100を引いた値
で現した。なお、実施例2、3の実験の際は圧縮面に断
面積3.46mm2 (直径2.1mm)の孔を2.5c
m間隔で設けた2重構造の盤2枚を用いこれを0.24
m3/分排気能力の真空ポンプに接続した。In this experiment, the amount of compression means the percentage of the thickness before processing with respect to the inter-panel distance at the end of the compression stroke previously set in the apparatus. The holding time refers to the time that the compression platen is held at that position when the compression platen reaches the set distance between the plates. The compression ratio is a percentage of the thickness of the foam test piece 24 hours after the end of the compression process to the original thickness. The deformed one also uses the size of the central part. The amount of deformation is 4
The difference between the average thickness of the middle part and the thickness of the center part of the piece was divided by the average of the thickness of the four pieces, multiplied by 100, and subtracted by 100. In the experiments of Examples 2 and 3, a hole having a cross-sectional area of 3.46 mm 2 (2.1 mm in diameter) was formed on the compression surface by 2.5 c.
Using two double-structure boards provided at intervals of m
It was connected to a vacuum pump with an evacuation capacity of m 3 / min.
【0024】表1に実施例1〜4と比較例1〜2の処理
条件と結果を示す。実施例1は発泡体に気孔を121個
設けたものを圧縮量90%で処理し、保持時間を10分
間としたもので結果の圧縮率は60.9%、変形量は
1.5%であった。実施例2は同じく気孔のみで減圧は
行わず90%まで圧縮し、ここで5分間保持時したもの
で圧縮率は45.3%、変形率は2.8%であった。実
施例3は実施例1に減圧操作を加えて行ったもので結果
は圧縮率47.7%、変形量は2.1%であった。実施
例4は実施例2と保持時間を5分から3分に変更した以
外は同様の実験であり、結果は圧縮率39.3%、変形
量は1.4%であった。Table 1 shows the processing conditions and results of Examples 1-4 and Comparative Examples 1-2. In Example 1, a foam having 121 pores was treated at a compression rate of 90% and the holding time was set to 10 minutes. The resulting compression rate was 60.9% and the deformation was 1.5%. there were. In Example 2, compression was performed to 90% without depressurization using only pores, and held for 5 minutes. The compression ratio was 45.3% and the deformation ratio was 2.8%. Example 3 was performed by adding a decompression operation to Example 1, and as a result, the compression ratio was 47.7% and the amount of deformation was 2.1%. Example 4 is the same experiment as Example 2 except that the holding time was changed from 5 minutes to 3 minutes, and the result was a compression ratio of 39.3% and a deformation amount of 1.4%.
【0025】[0025]
【表1】 [Table 1]
【0026】[比較例1〜2]一方、実施例1に気孔の
設置以外で同じ処理条件の従来公知の方法で行ったもの
が比較例1であるが、同じ保持時間で圧縮率は51.5
%と小さく、反面、変形は9.1%と中央部の膨らみが
大きく板状の部材としての問題のある物であった。比較
例2は保持時間を比較例の半分の5分で実施例2、3と
同じにして行ったが圧縮率は40.1%と低く、反面、
変形は7.8%と実施例2、3より3〜4倍大きかっ
た。[Comparative Examples 1 and 2] On the other hand, Comparative Example 1 was performed in the same manner as in Example 1 except that the pores were not provided and under the same processing conditions as in the prior art. 5
%, On the other hand, the deformation was 9.1%, and the bulge at the center was large, which was a problem as a plate-shaped member. Comparative Example 2 was performed in the same manner as in Examples 2 and 3 except that the holding time was 5 minutes, which is half of that of Comparative Example, but the compression ratio was as low as 40.1%.
The deformation was 7.8%, which was 3 to 4 times larger than Examples 2 and 3.
【0027】実施例4と比較例2は圧縮率が39.3%
と40.1%でほぼ同じで密度も18.5kg/m3と同
じものであるが、これに同じ密度の通常のEPSと圧縮
処理前の11.1kg/m3のEPSを加えて4種類の試
験体を準備し熱伝導率とJISK6767による圧縮永
久ひずみを比較測定した。その結果を表2に示す。これ
から、圧縮処理により熱伝導率、圧縮永久ひずみ共に未
処理の発泡体及び密度が同じ通常の発泡体により小さく
なり(改善され)かつ、比較例による処理のものとの対
比で本発明方法によるものは特性的になんら変わりない
ことが確認された。The compression ratio of Example 4 and Comparative Example 2 was 39.3%.
And 40.1%, which are almost the same and have the same density of 18.5 kg / m 3 , but with the addition of ordinary EPS of the same density and 11.1 kg / m 3 of EPS before compression processing, there are four types. Was prepared and the thermal conductivity and the compression set according to JIS K6767 were measured for comparison. Table 2 shows the results. From this, it can be seen that the compression treatment reduces (improves) the untreated foam and the ordinary foam having the same density in both the thermal conductivity and the compression set, and the method according to the present invention in comparison with the treatment according to the comparative example. It was confirmed that the characteristics did not change at all.
【0028】[実施例5〜9][比較例3〜7]表3に
は本発明と公知の方法を1秒、1分、3分、5分、10
分と保持時間を変えて圧縮率と変形率の面から比較した
結果を示す。本発明方法は気孔数121個、減圧度62
0mmHgで行い、圧縮速度は本発明実施例、比較例とも
35cm/分で行った。この結果から、いずれの実験にお
いても本発明の実施例が同じ保持時間の比較例に対して
圧縮率が大きくなること、一方で変形率が小さく優れて
いることが明らかとなった。[Examples 5 to 9] [Comparative Examples 3 to 7] Table 3 shows the method of the present invention and the known method for 1 second, 1 minute, 3 minutes, 5 minutes and 10 minutes.
The results of comparing the compression ratio and the deformation ratio by changing the minutes and the holding time are shown. The method of the present invention has 121 pores and a decompression degree of 62.
The compression was performed at 0 mmHg, and the compression speed was 35 cm / min in both the examples of the present invention and the comparative examples. From these results, it was clarified that, in each of the experiments, the examples of the present invention had higher compression ratios than the comparative examples having the same holding time, while the deformation ratio was small and excellent.
【0029】[0029]
【表2】 [Table 2]
【0030】[0030]
【表3】 [Table 3]
【0031】[0031]
【発明の効果】請求項1の方法で異方性スチレン系樹脂
発泡体が製造できる。請求項2の方法で高い圧縮率で変
形の少ない異方性スチレン系樹脂発泡体を容易に製造で
きる。請求項3の方法で異方性スチレン系樹脂発泡体を
より短い時間で圧縮処理して製造できる。請求項4の方
法で上記の方法の効果をより確実にして製造できる。請
求項5の方法で上記の方法の効果が特に大きくして製造
できる。According to the method of the first aspect, an anisotropic styrene resin foam can be produced. According to the method of the second aspect, it is possible to easily produce an anisotropic styrene resin foam having a high compression ratio and a small deformation. According to the method of the third aspect, the anisotropic styrenic resin foam can be produced by compressing in a shorter time. According to the method of claim 4, the effect of the above method can be produced more reliably. According to the method of the fifth aspect, the effect of the above method can be particularly increased to manufacture.
Claims (5)
け次いで発泡体を圧縮することを特徴とする異方性スチ
レン系樹脂発泡体の製造法。1. A method for producing an anisotropic styrene resin foam, comprising providing a plurality of pores in a styrene resin foam and then compressing the foam.
樹脂発泡体に断面積が0.5〜10mm2の複数の気孔
を設け次いで発泡体の初期の厚さの60〜5%となるま
で圧縮し、圧縮終了後の厚さが初期厚さに対し90〜1
0%となるように圧縮することを特徴とする請求項1記
載の異方性スチレン系樹脂発泡体の製造法。2. A styrene resin foam having a density of 7 to 50 kg / m 3 is provided with a plurality of pores having a cross-sectional area of 0.5 to 10 mm 2 , and then has a thickness of 60 to 5% of the initial thickness of the foam. And the thickness after compression is 90 to 1 with respect to the initial thickness.
The method for producing an anisotropic styrene resin foam according to claim 1, wherein the foam is compressed to 0%.
求項1又は2記載の異方性スチレン系樹脂発泡体の製造
法。3. The method for producing an anisotropic styrene resin foam according to claim 1, wherein the compressed surface is suctioned under reduced pressure during the compression step.
厚さが3cm以上で体積が4000cm3以上である請
求項1、2又は3記載の異方性スチレン系樹脂発泡体の
製造法。4. A process for producing anisotropic styrene resin foam of claim 1, wherein the thickness of the compressive direction the volume in 3cm or more and 4000 cm 3 or more styrenic foam before compression.
法−圧縮処理後の寸法)/圧縮処理前の寸法)×100
%が70%以上である請求項1、2、3又は4記載の異
方性スチレン系樹脂発泡体の製造法。5. A compression ratio at the time of compression processing ((dimension before compression processing−dimension after compression processing) / dimension before compression processing) × 100
5. The method for producing an anisotropic styrene resin foam according to claim 1, wherein the% is 70% or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9193636A JPH1134174A (en) | 1997-07-18 | 1997-07-18 | Production of anisotropic styrenic resin foam |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9193636A JPH1134174A (en) | 1997-07-18 | 1997-07-18 | Production of anisotropic styrenic resin foam |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH1134174A true JPH1134174A (en) | 1999-02-09 |
Family
ID=16311246
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9193636A Pending JPH1134174A (en) | 1997-07-18 | 1997-07-18 | Production of anisotropic styrenic resin foam |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH1134174A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20000072536A (en) * | 2000-09-08 | 2000-12-05 | 정갑철 | Manufacturing Method of Soft EPS Boards using Floor Impact Sound Insulation Materials in Apartment Houses |
| JP2012201820A (en) * | 2011-03-25 | 2012-10-22 | Sekisui Plastics Co Ltd | Expansion-molded product and production method therefor |
| JP2013525553A (en) * | 2010-04-29 | 2013-06-20 | ビーエーエスエフ ソシエタス・ヨーロピア | Method for producing compressed elastic foam material of melamine / formaldehyde resin system |
-
1997
- 1997-07-18 JP JP9193636A patent/JPH1134174A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20000072536A (en) * | 2000-09-08 | 2000-12-05 | 정갑철 | Manufacturing Method of Soft EPS Boards using Floor Impact Sound Insulation Materials in Apartment Houses |
| JP2013525553A (en) * | 2010-04-29 | 2013-06-20 | ビーエーエスエフ ソシエタス・ヨーロピア | Method for producing compressed elastic foam material of melamine / formaldehyde resin system |
| JP2012201820A (en) * | 2011-03-25 | 2012-10-22 | Sekisui Plastics Co Ltd | Expansion-molded product and production method therefor |
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