JPH07229097A - Cushioning material for molding press and its production - Google Patents
Cushioning material for molding press and its productionInfo
- Publication number
- JPH07229097A JPH07229097A JP16811393A JP16811393A JPH07229097A JP H07229097 A JPH07229097 A JP H07229097A JP 16811393 A JP16811393 A JP 16811393A JP 16811393 A JP16811393 A JP 16811393A JP H07229097 A JPH07229097 A JP H07229097A
- Authority
- JP
- Japan
- Prior art keywords
- elastic
- powder
- papermaking
- fiber
- paper
- 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 99
- 238000000465 moulding Methods 0.000 title claims description 20
- 238000004519 manufacturing process Methods 0.000 title claims description 11
- 238000000034 method Methods 0.000 claims abstract description 38
- 239000002245 particle Substances 0.000 claims abstract description 27
- 239000012784 inorganic fiber Substances 0.000 claims abstract description 16
- 239000011230 binding agent Substances 0.000 claims abstract description 11
- 239000000835 fiber Substances 0.000 claims description 81
- 239000000843 powder Substances 0.000 claims description 74
- 238000010298 pulverizing process Methods 0.000 claims description 28
- 239000000126 substance Substances 0.000 claims description 22
- 229920000642 polymer Polymers 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 16
- 239000002002 slurry Substances 0.000 claims description 15
- 238000004898 kneading Methods 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 10
- 239000002344 surface layer Substances 0.000 claims description 10
- 238000004073 vulcanization Methods 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims 1
- 229920001971 elastomer Polymers 0.000 abstract description 29
- 230000008859 change Effects 0.000 abstract description 22
- 230000008569 process Effects 0.000 abstract description 7
- 230000007423 decrease Effects 0.000 abstract description 4
- 239000000806 elastomer Substances 0.000 abstract description 3
- 239000000123 paper Substances 0.000 description 81
- 239000005060 rubber Substances 0.000 description 26
- 238000012937 correction Methods 0.000 description 25
- 239000000853 adhesive Substances 0.000 description 17
- 230000000181 anti-adherent effect Effects 0.000 description 17
- 239000011490 mineral wool Substances 0.000 description 12
- 239000007788 liquid Substances 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 239000004760 aramid Substances 0.000 description 9
- 229920003235 aromatic polyamide Polymers 0.000 description 9
- 239000010410 layer Substances 0.000 description 9
- 238000002156 mixing Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000000227 grinding Methods 0.000 description 8
- 238000010586 diagram Methods 0.000 description 7
- 239000004744 fabric Substances 0.000 description 7
- 239000002657 fibrous material Substances 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- -1 Polyethylene Polymers 0.000 description 5
- 229920001973 fluoroelastomer Polymers 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 230000005484 gravity Effects 0.000 description 5
- 229920002647 polyamide Polymers 0.000 description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
- 238000013329 compounding Methods 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000013013 elastic material Substances 0.000 description 4
- 239000010419 fine particle Substances 0.000 description 4
- 239000011737 fluorine Substances 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 239000004745 nonwoven fabric Substances 0.000 description 4
- 238000004080 punching Methods 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 229920002943 EPDM rubber Polymers 0.000 description 3
- 229920000459 Nitrile rubber Polymers 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 239000011324 bead Substances 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 239000004816 latex Substances 0.000 description 3
- 229920000126 latex Polymers 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 238000010008 shearing Methods 0.000 description 3
- 229920002545 silicone oil Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004709 Chlorinated polyethylene Substances 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004962 Polyamide-imide Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 239000004734 Polyphenylene sulfide Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 229920000800 acrylic rubber Polymers 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 229920005549 butyl rubber Polymers 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 229920006229 ethylene acrylic elastomer Polymers 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920002312 polyamide-imide Polymers 0.000 description 2
- 229920001230 polyarylate Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 229920000069 polyphenylene sulfide Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920002379 silicone rubber Polymers 0.000 description 2
- 239000004945 silicone rubber Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229920000106 Liquid crystal polymer Polymers 0.000 description 1
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004699 Ultra-high molecular weight polyethylene Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000027455 binding Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 229920005558 epichlorohydrin rubber Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000636 poly(norbornene) polymer Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001955 polyphenylene ether Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B30—PRESSES
- B30B—PRESSES IN GENERAL
- B30B15/00—Details of, or accessories for, presses; Auxiliary measures in connection with pressing
- B30B15/06—Platens or press rams
- B30B15/061—Cushion plates
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
- Paper (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、合成樹脂積層板、プリ
ント基板等のプレス成形に用いられる成形プレス用クッ
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 for molding press used for press molding of synthetic resin laminates, printed circuit boards and the like.
【0002】[0002]
【従来の技術】従来、この種のプレス用クッション材の
代表的なものとして、不織布製のもの及び耐熱抄造紙製
のものが知られている。2. Description of the Related Art Heretofore, as a typical example of this type of press cushion material, a non-woven material and a heat-resistant papermaking material have been known.
【0003】前者の不織布製のものとしては、例えば特
開昭55−101224号公報に見られるように、芳香
族ポリアミド繊維のバットを基布と共に複数層に積層し
てニードルパンチングにより結合一体化し、かつ熱処理
仕上げを施したものが公知である。As the former non-woven fabric, for example, as seen in JP-A-55-101224, batts of aromatic polyamide fiber are laminated with a base fabric into a plurality of layers and they are joined and integrated by needle punching, Moreover, those which have been subjected to heat treatment finish are known.
【0004】また、抄造紙製のものとしては、例えば特
公平2−60799号、実開昭62−60300号、特
開昭63−60715号、実開昭63−75329号公
報等の多くの例を見ることができるように、主として無
機質の微細繊維と、耐熱性芳香族系重合体のパルプ状物
質とを混合した水性スラリーから湿紙を抄造し、該湿紙
を必要枚数積層し脱水乾燥して一体化したものが最も一
般的に広く知られている。As the paper-made paper, there are many examples such as Japanese Examined Patent Publication No. 2-60799, Japanese Utility Model Publication No. 62-60300, Japanese Unexamined Patent Publication No. 63-60715, and Japanese Utility Model Publication No. 63-75329. As can be seen, a wet paper is made from an aqueous slurry in which mainly inorganic fine fibers and a pulp material of a heat-resistant aromatic polymer are mixed, and the necessary number of the wet paper is laminated and dehydrated and dried. The most commonly known one is the one that is integrated.
【0005】[0005]
【発明が解決しようとする課題】しかし、従来の上記不
織布製のクッション材にあっては、繊維の3次元配向に
より初期クッション特性に優れているものゝ、高温高圧
下で繰返し使用されると、著るしい厚みの減少とともに
クッション性が低下し、また熱伝導速度も変化して熱分
布が不均一になり、耐用寿命が短かいという本質的な欠
点を有している。加えて、厚さ分布の不均一、即ち目付
重量の不均一により、クッション性及び熱伝導速度の不
均一を生じ易く、成形積層板の表面に凹凸を生じる等の
悪影響を及ぼすおそれが大であった。However, the above-mentioned conventional non-woven cushion materials having excellent initial cushion properties due to the three-dimensional orientation of the fibers, when repeatedly used under high temperature and high pressure, Cushioning properties decrease with a remarkable decrease in thickness, and the heat conduction speed also changes, resulting in non-uniform heat distribution, which has the essential drawback of a short service life. In addition, the uneven thickness distribution, that is, the uneven weight is likely to cause uneven cushioning and uneven heat transfer rate, which may cause adverse effects such as unevenness on the surface of the molded laminate. It was
【0006】一方、抄造紙製のクッション材は、目付重
量が均一に製作でき、厚みムラ、および厚みの経時的変
化が少なく、耐熱性も良好なものとなしうる有利性を有
する。しかし反面、クッション材に本来的に求められる
クッション性に劣る。このため、熱盤の凹凸、鏡板の凹
凸、及び積層板の流動等に伴う圧力補償が十分にでき
ず、結果的に積層板に圧力不足によるボイドの発生等の
外観不良が出やすいという固有の欠点を有していた。On the other hand, the paper-made cushion material has the advantages that it can be manufactured with a uniform basis weight, there is little unevenness in thickness and change in thickness over time, and that it has good heat resistance. However, on the other hand, it is inferior in the cushioning property originally required for the cushioning material. Therefore, the pressure compensation due to the unevenness of the hot platen, the unevenness of the end plate, the flow of the laminated plate, etc. cannot be sufficiently performed, and as a result, the appearance defect such as the occurrence of voids due to insufficient pressure in the laminated plate is likely to occur. It had drawbacks.
【0007】そこで、この発明は、従来の耐熱抄造紙製
クッション材のもつ長所をそのまゝ保有せしめつゝ、そ
のクッション特性の改善をはかることを目的とする。更
に具体的には、目付重量のムラ、厚みの経時的変化が少
なく、しかも良好なクッション性を保有し、かつ圧縮復
元力に優れていて耐用寿命の顕著な増大をはかりうる成
形プレス用クッション材を提供することを目的とする。
更にはまた、かかるクッション材の好適な製造方法を提
供することを目的とする。Therefore, an object of the present invention is to allow the conventional cushioning material made of heat-resistant paper to retain its advantages and to improve its cushioning characteristics. More specifically, a cushioning material for a molding press, which has less uneven weight per unit area and less change in thickness over time, has good cushioning properties, has excellent compression restoring force, and can significantly increase the service life. The purpose is to provide.
Furthermore, it aims at providing the suitable manufacturing method of such a cushioning material.
【0008】[0008]
【課題を解決するための手段】この発明は、上記の目的
において、抄造紙のもつ優れた目付重量精度及び寸法安
定性を利用しながら、それに固有の欠点である低クッシ
ョン性を、抄造紙中に弾性体粉末を分散含有させること
によって改善したものである。In order to achieve the above object, the present invention utilizes the superior weight accuracy and dimensional stability of paper making, while at the same time providing the low cushioning property inherent in the paper making during paper making. This is improved by dispersing and containing an elastic powder.
【0009】即ち、この発明にかかる成形プレス用クッ
ション材は、有機繊維および/または無機繊維と、弾性
体粉末とを主成分として含み、上記弾性体粉末が全体に
均一に分散含有された抄造紙からなることを特徴とする
ものである。That is, the cushioning pad for molding press according to the present invention contains an organic fiber and / or an inorganic fiber and an elastic body powder as main components, and the elastic body powder is uniformly dispersed and contained in the whole papermaking paper. It is characterized by consisting of.
【0010】抄造紙の成分すなわち抄造紙材料として
は、上記必須の繊維及び弾性体粉末のほかに、更に要す
れば高分子パルプ状物質およびバインダーが任意の選択
または組合わせにおいて用いられる。As a component of the papermaking paper, that is, a papermaking material, in addition to the above-mentioned essential fibers and elastic powder, if necessary, a polymer pulp-like substance and a binder are used in any selection or combination.
【0011】なお、上記繊維を含まず、高分子パルプ状
物質及び弾性体粉末とから抄造した抄造紙についても検
討してみたが、このような抄造紙はクッション性が悪い
ため、成形プレス用クッション材には適さないことが実
験の結果判明した。A papermaking paper made from a polymer pulp-like substance and an elastic powder, which does not contain the above fibers, was also examined. However, since such papermaking paper has a poor cushioning property, a cushion for a molding press is used. As a result of the experiment, it was found that it was not suitable for wood.
【0012】また、この発明に係る上記成形プレス用ク
ッション材の製造方法は、弾性体コンパウンドに、粉粒
状または繊維状の固形粉砕媒体を加えて混練粉砕するこ
とにより平均粒子径250μm以下の弾性体粉末を作製
し、該弾性体粉末を、少なくとも有機繊維および/また
は無機繊維を含む抄造紙材料を離解した水性スラリーに
分散させ、該水性スラリーから前記弾性体粉末が内部に
均一に分散した抄造紙に抄造することを特徴とするもの
である。In the method for producing a cushioning material for molding press according to the present invention, an elastic body having an average particle diameter of 250 μm or less is obtained by adding a granular or fibrous solid pulverizing medium to an elastic body compound and kneading and pulverizing. A powder is prepared, the elastic powder is dispersed in an aqueous slurry obtained by disaggregating a paper-making paper material containing at least organic fibers and / or inorganic fibers, and the elastic powder is uniformly dispersed in the aqueous slurry from the aqueous slurry. It is characterized by being made into paper.
【0013】この発明の更に他の特徴は、以下に述べる
構成の具体的な説明によって逐次明らかにされるであろ
う。Still another feature of the present invention will be successively clarified by the detailed description of the configuration described below.
【0014】[0014]
(繊維材料)抄造紙の必須成分として用いられる繊維
は、有機繊維または無機繊維のいずれであっても良く、
あるいはそれらを混合して用いても良い。(Fiber material) The fiber used as an essential component of the papermaking paper may be either an organic fiber or an inorganic fiber,
Alternatively, they may be mixed and used.
【0015】使用可能な有機繊維として、例えばポリア
ミド繊維、芳香族ポリアミド繊維、フェノール繊維、ポ
リフェニレンサルファイド繊維、ポリイミド繊維、ポリ
アミドイミド繊維、ポリエステル繊維、芳香族ポリエス
テル繊維、ポリアリレート繊維、ふっ素繊維、等を挙げ
ることができる。また、無機繊維としては、ガラス繊
維、スラグウール繊維、ロックウール繊維、炭素繊維、
シリカ繊維、炭化珪素繊維、アルミナ繊維、アルミナシ
リケート繊維、ウオーラストナイト繊維、ジルコニア繊
維、金属繊維、等を挙げることができる。これらの中で
も、特に価格、耐熱性の点からはスラグウール繊維、ロ
ックウール繊維を、また重量、耐熱性の点からは芳香族
ポリアミド繊維を好適に用いることができ、クッション
材の使用条件等に応じてそれらのうちから選択使用する
ことが推奨される。Examples of usable organic fibers include polyamide fibers, aromatic polyamide fibers, phenol fibers, polyphenylene sulfide fibers, polyimide fibers, polyamideimide fibers, polyester fibers, aromatic polyester fibers, polyarylate fibers, and fluorine fibers. Can be mentioned. Further, as the inorganic fiber, glass fiber, slag wool fiber, rock wool fiber, carbon fiber,
Examples thereof include silica fiber, silicon carbide fiber, alumina fiber, alumina silicate fiber, wollastonite fiber, zirconia fiber, and metal fiber. Among these, slag wool fibers and rock wool fibers can be preferably used from the viewpoint of price and heat resistance, and aromatic polyamide fibers can be preferably used from the viewpoint of weight and heat resistance. It is recommended to select and use them accordingly.
【0016】有機無機を問わず、繊維径1〜30μm、
繊維長300〜15,000μmの範囲の繊維を使用す
べきである。Fiber diameter of 1 to 30 μm, regardless of organic or inorganic,
Fibers with fiber lengths in the range 300 to 15,000 μm should be used.
【0017】繊維径が1μm未満では、濾水性が悪くな
り、厚物の抄紙が困難でクッション材の製造能率の点で
好ましくないのみならずクッション性が悪くなり好まし
くない。また30μmをこえると、抄造紙における繊維
の絡みが不足し、特に紙層間剥離強度が弱くなるため、
耐用寿命が短かくなる。最も好ましい繊維径は、5〜2
0μm程度である。When the fiber diameter is less than 1 μm, the drainage is poor, making thick paper is difficult and not only unfavorable in terms of the cushioning material manufacturing efficiency, but also unfavorable in cushioning property. On the other hand, when it exceeds 30 μm, the entanglement of fibers in the papermaking paper is insufficient, and the paper interlaminar peel strength becomes particularly weak.
The service life is shortened. Most preferred fiber diameter is 5 to 2
It is about 0 μm.
【0018】繊維長が300μm未満では、やはり繊維
の絡みが不足し、抄造紙ひいてはクッション材の抗折力
が弱くなって作業性、耐用寿命を悪くする。逆に繊維長
が15,000μmをこえて長いと、離解時に繊維の毛
玉ができ易く、抄造紙表面の地合いが悪くなる。また目
付重量の不均一を生じ易く厚み精度が悪くなり易い。好
ましい繊維長は、およそ1,000〜7,000μmの
範囲である。When the fiber length is less than 300 μm, the entanglement of the fibers is insufficient, and the transverse rupture strength of the papermaking paper and eventually the cushioning material is weakened to deteriorate workability and service life. On the contrary, when the fiber length is longer than 15,000 μm, pills of fibers are likely to be formed at the time of disaggregation and the texture of the surface of the papermaking paper is deteriorated. Further, the weight per unit area is likely to be non-uniform, and the thickness accuracy is likely to deteriorate. The preferred fiber length is in the range of approximately 1,000 to 7,000 μm.
【0019】(弾性体粉末)弾性体粉末は、抄造紙に良
好なクッション性を付与するものである。従って、それ
自体に好ましい弾性を保有するものでなければならな
い。従って、かかる観点から加硫後の硬度としてJIS
A20〜98度の硬度を有するような弾性材料が用い
られる。硬度が20度未満では、クッション材の圧縮変
形量が過大になり、弾性復元力の乏しいものとなるため
好ましくない。また98度をこえる弾性体粉末では、そ
れ自体の弾性が不足し、クッション材に良好なクッショ
ン性を付与することができない。最も好ましい硬度の範
囲は、概ね60〜80度である。弾性体粉末は、上記硬
度を有するものであれば、その材料の種類を問わない。
ゴム材料であっても良いし、熱可塑性樹脂エラストマー
材料であっても良い。前者の例としては、例えば、天然
ゴム、イソプレンゴム、スチレンブタジエンゴム、ポリ
ブタジエンゴム、クロロプレンゴム、アクリロニトリル
ブタジエンゴム、水素化ニトリルゴム、ブチルゴム、エ
チレンプロピレンゴム、ポリウレタンゴム、シリコーン
ゴム、ふっ素ゴム、クロロスルホン化ポリエチレン、塩
素化ポリエチレン、アクリルゴム、エピクロロヒドリン
ゴム、多硫化ゴム、プロピレンオキシゴム、エチレンア
クリルゴム、エチレン酢酸ビニル共重合体、ポリノルボ
ルネンゴム、アルフィンゴム、等を用いることができ
る。また後者のエラストマー材料としては、例えば、ポ
リスチレン系、ポリオレフィン系、ポリウレタン系、ポ
リエステル系、ポリアミド系、塩化ビニル系、1,2−
ポリブタジエン系、ポリイソプレン系、塩素化ポリエチ
レン系、ふっ素ゴム系、等の各種の材料を用いることが
できる。(Elastic Body Powder) The elastic body powder imparts good cushioning properties to the papermaking paper. Therefore, it must possess desirable elasticity in itself. Therefore, from such a viewpoint, the hardness after vulcanization is JIS
An elastic material having a hardness of A20 to 98 degrees is used. If the hardness is less than 20 degrees, the amount of compressive deformation of the cushion material becomes excessive and the elastic restoring force becomes poor, which is not preferable. Further, an elastic powder having a temperature of more than 98 degrees is insufficient in elasticity of itself and cannot provide good cushioning properties to the cushion material. The most preferable hardness range is approximately 60 to 80 degrees. The elastic powder may be of any type as long as it has the above hardness.
It may be a rubber material or a thermoplastic resin elastomer material. Examples of the former include, for example, natural rubber, isoprene rubber, styrene butadiene rubber, polybutadiene rubber, chloroprene rubber, acrylonitrile butadiene rubber, hydrogenated nitrile rubber, butyl rubber, ethylene propylene rubber, polyurethane rubber, silicone rubber, fluorine rubber, chlorosulfone. Polyethylene, chlorinated polyethylene, acrylic rubber, epichlorohydrin rubber, polysulfide rubber, propyleneoxy rubber, ethylene acrylic rubber, ethylene vinyl acetate copolymer, polynorbornene rubber, alfin rubber and the like can be used. Examples of the latter elastomer material include polystyrene-based, polyolefin-based, polyurethane-based, polyester-based, polyamide-based, vinyl chloride-based, 1,2-
Various materials such as polybutadiene-based, polyisoprene-based, chlorinated polyethylene-based, and fluororubber-based materials can be used.
【0020】上記のような種々の弾性材料のなかでも、
特にクッション材が熱プレスに用いられるものである場
合、耐熱性に優れた弾性材料を選択使用すべきである。
かかる耐熱性弾性材料としては、ゴム材料の中では水素
化ニトリルゴム、ブチルゴム、エチレンプロピレンゴ
ム、シリコーンゴム、ふっ素ゴム、アクリルゴム、エチ
レンアクリルゴム、アルフィンゴムを好適に用いること
ができる。熱可塑性エラストマー材料の中では、ポリオ
レフィン系、ポリエステル系、ポリアミド系、ふっ素ゴ
ム系の材料を好適に用いることができる。Among the various elastic materials described above,
Especially when the cushioning material is used for hot pressing, an elastic material having excellent heat resistance should be selected and used.
As the heat resistant elastic material, hydrogenated nitrile rubber, butyl rubber, ethylene propylene rubber, silicone rubber, fluoro rubber, acrylic rubber, ethylene acrylic rubber, and alfin rubber can be preferably used among rubber materials. Among the thermoplastic elastomer materials, polyolefin-based, polyester-based, polyamide-based, and fluororubber-based materials can be preferably used.
【0021】弾性体粉末は、その粒度もクッション材の
性能に大きく影響を及ぼす。而して、平均粒径20〜2
50μmの範囲のものを用いるべきである。平均粒径が
20μm未満の場合、抄造紙の繊維どうしの間に弾性体
粉末が埋まってしまい、良好なクッション性が得られな
くなる。これを防止するためには、弾性体粉末は、その
粒子径が繊維の径の数倍以上であるものを選択使用すべ
きである。しかしながら、平均粒子径が250μmをこ
えて大きい場合、抄紙工程で弾性体粉末の沈殿やヘッド
ボックス内での水流による偏在化が生じ、クッション性
の不均一の原因となる抄造紙内での分散の不均一及び紙
表面の地合い不良が生じるため好ましくない。最も好適
な粒度範囲は、平均粒径30〜90μmである。The particle size of the elastic powder also greatly affects the performance of the cushion material. Thus, the average particle size is 20 to 2
A range of 50 μm should be used. If the average particle size is less than 20 μm, the elastic powder is buried between the fibers of the papermaking paper, and good cushioning properties cannot be obtained. In order to prevent this, the elastic powder should have a particle diameter several times larger than the diameter of the fiber. However, when the average particle size is larger than 250 μm, precipitation of elastic powder or uneven distribution due to water flow in the head box occurs in the paper making process, which causes unevenness of cushioning property in paper making. It is not preferable because unevenness and poor texture of the paper surface occur. The most preferred particle size range is an average particle size of 30 to 90 μm.
【0022】上記のような粒径範囲の弾性体粉末の製造
は、弾性体コンパウンドから機械粉砕、あるいは冷凍粉
砕の公知の粉砕方法で粉砕することによっても行うこと
ができる。しかし、機械粉砕は、粒径200〜400μ
mの範囲の粉砕しかできず、本発明に必要な250μm
以下の微粒子粉体の収率に劣るため、好ましくない。一
方、冷凍粉砕は、本発明に最も好適とする30〜90μ
mの粒径範囲に較べ、やゝ粒径の大きい100〜250
μmの範囲の粉砕しかできないため、抄造紙に最も好ま
しい地合いを確保する上からは最善の方法とはいえな
い。The elastic powder having a particle size range as described above can also be produced by pulverizing the elastic compound with a known pulverizing method such as mechanical pulverization or freeze pulverization. However, the mechanical crushing has a particle size of 200 to 400 μ.
250 μm required for the present invention, which can only pulverize in the range of m
It is not preferable because the yield of the following fine particle powder is poor. On the other hand, freeze pulverization is most suitable for the present invention, 30 to 90μ.
Compared to the particle size range of m, the particle size is slightly larger, 100-250
Since it can only grind in the range of μm, it cannot be said to be the best method from the viewpoint of securing the most favorable texture for papermaking.
【0023】上記2つの粉砕方法に対し、混練粉砕によ
る方法が最も好適である。即ちこの方法は、弾性体コン
パウンドにせん断力を付与しうる固形粉砕媒体と、必要
に応じて液状防着剤とを混合して、ニーダー、インター
ナルミキサー等の密閉式混練機で混練りするものであ
り、粉砕媒体の形状と防着剤の種類の適当な選択によ
り、粒径10〜250μmの微粒子の粉砕が可能であ
り、かつ粉砕コストの点でも好ましい。The method of kneading and pulverizing is most suitable for the above two pulverizing methods. That is, this method is a method in which a solid pulverizing medium capable of imparting a shearing force to an elastic compound is mixed with a liquid anti-adhesive agent, and kneaded with a kneader, an internal mixer or other closed kneader. By appropriately selecting the shape of the grinding medium and the kind of the anti-adhesive agent, it is possible to grind fine particles having a particle diameter of 10 to 250 μm, and it is also preferable in terms of grinding cost.
【0024】上記粉砕媒体は、弾性体コンパウンドにせ
ん断力を付与しうる固形物であれば粉粒状あるいは繊維
状のいずれであっても良いが、弾性体に補強作用を与え
ない大きさを有するものであることが必要である。この
ため、粉粒状物にあっては粒子径2〜100μmのもの
を、繊維状物にあっては繊維径2〜100μmの大きさ
で、かつ混練機のせん断力で弾性体とともに容易に微細
化されうる脆い材料のものを用いるべきである。The crushing medium may be powdery or fibrous as long as it is a solid substance capable of imparting a shearing force to the elastic compound, but has a size that does not give a reinforcing action to the elastic body. It is necessary to be. For this reason, a powder-granular material having a particle diameter of 2 to 100 μm and a fibrous material having a fiber diameter of 2 to 100 μm can be easily miniaturized together with the elastic body by the shearing force of the kneader. The brittle material that can be used should be used.
【0025】粉砕媒体として、具体的には、砂糖粉末、
塩化ナトリウム粉末等の水に可溶性の粒子を用いても良
い。この場合、弾性体粉末の製造後、抄紙前または抄紙
時に水に溶解させて上記粉砕媒体を取除くものとするこ
とが可能となる。しかし最も一般的かつ好適には、粉砕
媒体としては、ガラス繊維、スラグウール繊維、ロック
ウール繊維、シリカ繊維等の繊維状物、あるいはガラス
ビーズ、シリカ粉末、石炭粉末、炭酸カルシウム、フェ
ライト粉末等の粉粒物が使用される。繊維状物は、混練
粉砕することによって弾性体とともに容易に微細化さ
れ、その繊維長が弾性体粉末の粒子径と同程度、すなわ
ち10〜250μmの微粒子となる。繊維状物あるいは
粒状物を使用した場合、その大部分はゴム粒子中に入り
込むか又は付着し、それ以外の一部は抄造紙中に微粒子
状で存在することとなる。また粒状物のなかでも中空の
ガラスビーズの使用は、抄造紙の軽量化、熱伝導性の抑
制に役立つと共に、粒子径の揃ったものを入手し易いこ
とから、弾性体粉末の粒子径を均一なものとするのに有
利である。As the grinding medium, specifically, sugar powder,
Water-soluble particles such as sodium chloride powder may be used. In this case, after the production of the elastic powder, it becomes possible to dissolve the pulverizing medium by dissolving it in water before or during papermaking. However, most commonly and preferably, as the grinding medium, glass fibers, slag wool fibers, rock wool fibers, fibrous materials such as silica fibers, or glass beads, silica powder, coal powder, calcium carbonate, ferrite powder, etc. Granules are used. The fibrous material is easily finely pulverized together with the elastic body by kneading and pulverizing, and the fibrous material becomes fine particles having a fiber length similar to the particle diameter of the elastic body powder, that is, 10 to 250 μm. When fibrous or granular materials are used, most of them enter into or adhere to the rubber particles, and the other parts are present in fine particles in the papermaking paper. In addition, the use of hollow glass beads among the granules helps to reduce the weight of the papermaking paper and suppress thermal conductivity, and it is easy to obtain those with a uniform particle size, so the particle size of the elastic powder is uniform. Which is advantageous.
【0026】粉砕媒体の配合量は、弾性体コンパウンド
100重量部に対し、40〜400重量部とするのが好
ましい。40重量部未満では、弾性体コンパウンドの粉
砕作用が不十分なものとなり、十分な微細化ができな
い。一方、400重量部をこえて過多に配合すると、弾
性体粉末量の相対的な減少により、抄造紙の弾性、クッ
ション性が不十分なものとなる。The compounding amount of the grinding medium is preferably 40 to 400 parts by weight with respect to 100 parts by weight of the elastic compound. If it is less than 40 parts by weight, the crushing action of the elastic compound becomes insufficient, and sufficient miniaturization cannot be achieved. On the other hand, if the amount is too much over 400 parts by weight, the elasticity and cushioning property of the papermaking paper will be insufficient due to the relative decrease in the amount of elastic powder.
【0027】混練粉砕に際しては、必要に応じて液状防
着剤が添加される。液状防着剤は、粉砕媒体によって粉
砕された弾性体の切断面に付着し、その再凝着を防止し
て、微粉砕化を促進する作用を果す。かかる液状防着剤
としてはシリコーンオイル、ふっ素オイル等の非水系界
面活性剤、または水溶性界面活性剤が用いられる。その
添加量は、弾性体コンパウンドと粉砕媒体の総量100
重量部に対し、3重量部以下とすべきである。3重量部
をこえて過多に用いると、抄造時に泡立ち等の悪影響を
与えるのみならず、抄造後の紙の使用中に防着剤が滲出
するおそれがある。At the time of kneading and pulverization, a liquid anti-adhesive agent is added if necessary. The liquid anti-adhesive agent adheres to the cut surface of the elastic body crushed by the crushing medium, prevents re-adhesion of the elastic body, and promotes fine pulverization. As the liquid anti-adhesive agent, a non-aqueous surfactant such as silicone oil or fluorine oil, or a water-soluble surfactant is used. The total amount of the elastic compound and the grinding medium is 100.
It should be 3 parts by weight or less with respect to parts by weight. If it is used in excess of 3 parts by weight, not only adverse effects such as foaming may occur at the time of papermaking but also the anti-adhesion agent may exude during use of the paper after papermaking.
【0028】(高分子パルプ状物質)抄造材料には、上
記した必須成分としての繊維材料及び弾性体粉末のほか
に、更に高分子パルプ状物質を所要量添加配合すること
が好ましい。こゝに、高分子パルプ状物質とは、高分子
原料に機械的または化学的な微細化処理を施して、高分
子繊維状集合体となすと共に、その全部または一部をフ
ィブリル化させてくもの巣状に枝分かれさせたものであ
る。従って、かかるパルプ状物質の配合は、抄造紙のク
ッション性を増大すると共に、フィブリル化繊維部分の
バインディング作用により抄造紙の機械的強度の向上に
有効に機能する。(Polymer pulp-like substance) In addition to the above-mentioned fiber material and elastic powder as the essential components, it is preferable to add a required amount of polymer pulp-like substance to the papermaking material. Here, the polymer pulp-like substance means a polymer raw material that is mechanically or chemically refined to form a polymer fibrous aggregate, and all or part of the polymer is fibrillated. It is a nest-shaped branch. Therefore, the addition of such a pulp-like substance not only increases the cushioning property of the papermaking paper, but also effectively functions to improve the mechanical strength of the papermaking paper due to the binding action of the fibrillated fiber portion.
【0029】パルプ状物質の高分子材料の具体例として
は、天然物では、セルロースパルプを、合成物では芳香
族ポリアミド、芳香族ポリエステル、ポリアミド、ポリ
イミド、ポリアミドイミド、ポリエステル、ポリオレフ
ィン、ポリカーボネート、ふっ素樹脂、フェノール、ポ
リアセタール、変性ポリフェニレンエーテル、ポリブチ
レンテレフタレート、超高分子量ポリエチレン、ポリサ
ルフォン、ポリエーテルサルフォン、ポリフェニレンサ
ルファイド、ポリアリレート、ポリエーテルイミド、ポ
リエーテルエーテルケトン、液晶ポリマー、およびこれ
らの変性樹脂並びにこれらの混合物をあげることができ
る。Specific examples of the polymer material of the pulp-like substance include cellulose pulp as a natural material and aromatic polyamide, aromatic polyester, polyamide, polyimide, polyamideimide, polyester, polyolefin, polycarbonate, fluororesin as a synthetic material. , Phenol, polyacetal, modified polyphenylene ether, polybutylene terephthalate, ultra high molecular weight polyethylene, polysulfone, polyether sulfone, polyphenylene sulfide, polyarylate, polyetherimide, polyetheretherketone, liquid crystal polymer, and modified resins thereof and these Can be a mixture of.
【0030】高分子パルプ状物質の配合量は、前記の有
機および/または無機繊維と、高分子パルプ状物質と、
弾性体粉末との三者を合わせた体積に対して、50vol
%以下とすべきであり、好適には5〜20vol %の範囲
である。50vol %をこえてパルプ状物質を多く配合す
ると、クッション性が低下し、かつ、コスト的にも高く
なる。The blending amount of the polymer pulp-like substance is such that the above-mentioned organic and / or inorganic fibers, the polymer pulp-like substance and
50vol for the combined volume of elastic powder
% Or less, preferably in the range of 5 to 20 vol%. If a large amount of pulp-like substance is added to the content of more than 50 vol%, the cushioning property will be deteriorated and the cost will be increased.
【0031】また、パルプ状物質は,濾水値において1
〜100秒の範囲に調整したものを用いるのが好適であ
る。濾水値が100秒をこえるものでは、一度に厚物の
湿紙を抄造することが困難であり、ひいては薄く抄造し
た湿紙を複数枚重ね合わせて所要厚みの抄造紙を得るも
のとする必要が生じるため、抄造能率上好ましくない。
こゝに、本明細書でいう上記濾水値とは、パルプ状物質
を0.3%の水分散液(20℃)に調整し、これを1リ
ットル採取したスラリーを、底に78メッシュの金網を
張った内径102mmの円筒容器に移したとき、濾液が
500ml得られるに要する時間を秒であらわしたもの
である。The pulp-like substance has a drainage value of 1
It is preferable to use the one adjusted to the range of 100 seconds. If the drainage value exceeds 100 seconds, it is difficult to make a thick wet paper at a time, and it is necessary to stack a plurality of thin wet papers to obtain a paper having a required thickness. This is not preferable in terms of papermaking efficiency.
Here, the above-mentioned drainage value as used in the present specification means that a pulp-like substance is adjusted to a 0.3% aqueous dispersion (20 ° C.), and 1 liter of this slurry is taken to prepare a 78-mesh slurry at the bottom. When transferred to a cylindrical container having an inner diameter of 102 mm and covered with a wire net, the time required for obtaining 500 ml of the filtrate is expressed in seconds.
【0032】(バインダー)バインダーは、抄造紙の層
間剥離強度を上げるのに有効なものであるが、反面該抄
造紙をクッション材として使用する際の昇温速度を高
め、弾性復元力を低下するおそれがあるため、添加する
場合にも比較的少ない量の範囲で用いるべきである。従
って、有機繊維および/または無機繊維と、高分子パル
プ状物質と、弾性体粉末との三者を合わせた体積100
vol %に対して、せいぜい10vol %以下の範囲で用い
るべきであり、好適には7vol %以下の範囲とすること
が望ましい。(Binder) The binder is effective for increasing the delamination strength of the papermaking paper, but on the other hand, it raises the temperature rising rate when the papermaking paper is used as a cushioning material and reduces the elastic restoring force. Therefore, even if added, it should be used in a relatively small amount range. Therefore, the total volume of the organic fiber and / or inorganic fiber, the polymer pulp-like substance, and the elastic powder is 100.
It should be used in the range of at most 10 vol% with respect to vol%, and preferably in the range of 7 vol% or less.
【0033】バインダーの具体例としては、例えば、エ
ポキシ樹脂系、シリコーン樹脂系、フェノール樹脂系、
アクリル樹脂系等の熱硬化性樹脂を挙げることができ
る。その形態は粒状、ラテックス、エマルジョンのいず
れでも良い。Specific examples of the binder include, for example, epoxy resin type, silicone resin type, phenol resin type,
A thermosetting resin such as an acrylic resin can be used. The form may be granular, latex or emulsion.
【0034】(抄紙)上記抄造材料による抄造紙の抄造
は、従来の常法によって行い得る。即ち、繊維及び必要
に応じて添加する高分子パルプ状物質を混合して離解し
た水性スラリーに弾性体粉末を均一分散させ、長網式、
円網式、傾斜型ワイヤー式等の抄造機を用いて好ましく
は厚物の湿紙を抄造し、脱水および乾燥させて厚物の抄
造紙に製造する。または、薄物に抄造した湿紙を所要枚
数重ね合わせ、加熱加圧下に脱水乾燥させるものとして
も良い。(Papermaking) Papermaking of the papermaking paper with the above-mentioned papermaking material can be carried out by a conventional method. That is, the elastic powder is uniformly dispersed in an aqueous slurry obtained by mixing and disintegrating fibers and a polymer pulp-like substance to be added if necessary, and a fourdrinier type,
A thick wet paper is preferably made into a paper using a paper making machine such as a cylinder type or inclined wire type machine, and dehydrated and dried to produce a thick paper. Alternatively, the required number of wet paper sheets formed into thin sheets may be stacked and dehydrated and dried under heat and pressure.
【0035】ここに、弾性体粉末の配合量は、有機繊維
および/または無機繊維と、高分子パルプ状物質と、弾
性体粉末との三者を合わせた体積に対して、10〜95
vol%に設定すべきである。これが95vol %をこえて
過多に配合されると、弾性復元力は向上するものゝ耐圧
縮性、機械的強度に劣るものとなり好ましくない。逆に
10vol %未満では所期する良好なクッション性、弾性
復元力を実現することができない。より好ましい範囲は
40〜92vol %である。もっとも、当該抄造紙が、後
述する実施例に示すように、クッション材に製造するさ
いに他の抄造紙と積層接着するための接着機能を求めら
れるようなものである場合には、比較的多くの弾性体粉
末を分散させたものとするのが有利であり、専らにクッ
ション機能のみを求めて用いられるようなものである場
合には、相対的に少ない量の弾性体粉末を分散含有させ
たものとするのが好ましい。前者の接着用の抄造紙にあ
っては、最も好ましい弾性体粉末の配合量は50〜92
vol %であり、クッション用の抄造紙にあっては40〜
65vol %である。The amount of the elastic powder blended is 10 to 95 based on the combined volume of the organic fibers and / or inorganic fibers, the polymeric pulp-like substance, and the elastic powder.
It should be set to vol%. If this amount is excessively mixed in excess of 95 vol%, the elastic restoring force is improved, but the compression resistance and mechanical strength are deteriorated, which is not preferable. On the other hand, if it is less than 10 vol%, the desired good cushioning property and elastic restoring force cannot be realized. A more preferable range is 40 to 92 vol%. However, as shown in the examples described later, when the papermaking paper is required to have an adhesive function for laminating and adhering to another papermaking paper when it is manufactured into a cushioning material, it is relatively often used. It is advantageous to disperse the elastic body powder of 1., and when it is used exclusively for the cushion function, a relatively small amount of elastic body powder is dispersed and contained. Preferably. In the former papermaking paper for adhesion, the most preferable blending amount of elastic body powder is 50 to 92.
vol%, and 40-for paper made of cushions
It is 65 vol%.
【0036】(クッション材の製作)上記によって製作
される抄造紙は、これを単独でクッション材に使用して
も良いが、一般的にはその複数枚を重ねて加熱加圧によ
り積層し、所要厚みに構成したり、更にはその上下両面
に、離型性材料からなる表層材を積層接着して実用に供
される。表層材としては、公知の任意の表層材、例え
ば、織布、不織布、紙又はこれらのいずれかに改質剤を
含浸或いは塗布したもの又は耐熱性合成樹脂からなる
板、シート、フィルム又は金属箔等を用いることが可能
である。(Production of Cushion Material) The papermaking paper produced as described above may be used alone as a cushion material, but generally, a plurality of paper sheets are stacked and laminated by heating and pressurization. It is put to practical use by forming it to a thickness, and further laminating and adhering a surface layer material made of a releasable material on both upper and lower surfaces thereof. As the surface layer material, any known surface layer material, for example, woven fabric, non-woven fabric, paper, or any of these impregnated or coated with a modifier, or a plate, sheet, film or metal foil made of a heat resistant synthetic resin. Etc. can be used.
【0037】[0037]
実施例1 抄紙材料として、ロックウール繊維と、冷凍粉砕法によ
って得たEPDM(エチレンプロピレンターポリマー)
からなる弾性体粉末と、パルプ状物質と、そしてバイン
ダーとを主成分に用いたものである。Example 1 Rockwool fiber as a papermaking material and EPDM (ethylene propylene terpolymer) obtained by a freeze pulverization method
An elastic powder consisting of, a pulp-like substance, and a binder are used as main components.
【0038】弾性体粉末は、次の方法で製造した。即
ち、下記表1に示す配合材料を用い、バッチ式インター
ナルミキサーで混練したのち、ペレタイザーでペレット
化し、高速回転型の微粉砕機(ターボミル)を用いて冷
凍粉砕した。冷凍粉砕時に、固体防着剤としてタルク
を、前記配合材料100重量部に対して11.3重量部
の割合に添加した。そして、得られた粉末を35メッシ
ュの篩で分級し、平均粒径220μm、加硫後の硬度
(ショアA)70度、比重1.2の未加硫ゴム粉末とし
た。The elastic powder was manufactured by the following method. That is, the compounding materials shown in Table 1 below were kneaded with a batch type internal mixer, pelletized with a pelletizer, and frozen and pulverized with a high-speed rotary fine pulverizer (turbo mill). At the time of freeze-grinding, talc was added as a solid anti-adhesive at a ratio of 11.3 parts by weight to 100 parts by weight of the compounded material. Then, the obtained powder was classified with a 35-mesh sieve to obtain an unvulcanized rubber powder having an average particle size of 220 μm, a hardness (Shore A) of 70 degrees after vulcanization, and a specific gravity of 1.2.
【0039】[0039]
【表1】 次いで、次のようにして抄紙を行った。先ず、ビーター
を用いて、ロックウール繊維(平均繊維径5μm、平均
繊維長7mm)を多量の水とともに離解し、繊維を水中
に均一に分散させたのち、フィブリル化した芳香族ポリ
アミドからなるパルプ状物質を加え、同様に分散させ
た。そして、これに上記弾性体粉末と分散剤とを加えて
同様に分散させ、得られた一次スラリーをパルパーに投
入し、ラテックス系のバインダーを加えて最終離解を行
った。そしてこのスラリーをチェストに投入し、水を加
えて濃度調整を行うと共に、凝集剤を加えてフロック調
整を行って最終スラリーとしたのち、このスラリーを長
網抄紙機のワイヤー上に流し込んで湿紙を形成し、脱
水、乾燥させて目付重量700g/m2 の抄造紙を製作
した。[Table 1] Then, papermaking was performed as follows. First, using a beater, rockwool fibers (average fiber diameter 5 μm, average fiber length 7 mm) were disintegrated together with a large amount of water, and the fibers were uniformly dispersed in the water, and then pulped from fibrillated aromatic polyamide. Material was added and similarly dispersed. Then, the elastic powder and the dispersant were added to and dispersed in the same manner, and the obtained primary slurry was put into a pulper, and a latex binder was added to perform final disaggregation. Then, this slurry is put into a chest, water is added to adjust the concentration, and a flocculant is added to adjust the flocs to obtain a final slurry, which is then poured onto a wire of a Fourdrinier paper machine to obtain a wet paper web. Was formed, dehydrated and dried to produce a papermaking paper having a basis weight of 700 g / m 2 .
【0040】ここに、抄紙材料の配合割合は下記の表2
の通りとし、弾性体粉末の分散含有量の相対的に少ない
抄造紙(1)と、それの相対的に多い抄造紙(2)との
2種類を作製した。The mixing ratio of the papermaking material is shown in Table 2 below.
As described above, two types of paper were prepared: a papermaking paper (1) having a relatively low elastic powder content and a papermaking paper (2) having a relatively high elastic powder content.
【0041】[0041]
【表2】 上記によって得られた2種類の抄造紙(1)、(2)を
図1に示す態様に重ね、更に上下両面に表層材(1
1)、(11)を重ねて、温度175℃、時間70分、
圧力10kg/cm2 でプレスして、抄造紙中に含む未
加硫ゴム粉末(EPDM)を加硫させると同時に全体を
積層一体化し、試料No. 1の成形プレス用クッション材
を得た。なお表層材(11)は、ガラスクロスの両面に
ふっ素ゴムを塗布し、更にその片面(離型面側)に芳香
族アクリル樹脂を塗布したものを用いた。[Table 2] The two types of papermaking papers (1) and (2) obtained as described above were stacked on the embodiment shown in FIG. 1, and the surface layer material (1
1) and (11) are overlaid, the temperature is 175 ° C., the time is 70 minutes,
By pressing at a pressure of 10 kg / cm 2 , the unvulcanized rubber powder (EPDM) contained in the papermaking paper was vulcanized and, at the same time, the whole was laminated and integrated to obtain a cushioning pad for molding press of Sample No. 1. The surface layer material (11) used was one in which fluororubber was applied to both sides of glass cloth, and aromatic acrylic resin was applied to one side (release side) of the glass cloth.
【0042】実施例2 抄紙材料として、ロックウール繊維と、混練粉砕法によ
って製造したEPDM製の弾性体粉末と、パルプ状物質
および/またはバインダーとを主成分に用いたものであ
る。Example 2 As a papermaking material, rockwool fiber, EPDM elastic powder produced by the kneading and pulverizing method, and a pulp-like substance and / or a binder were used as main components.
【0043】弾性体粉末の製造は、前記実施例1と同様
の配合のゴムコンパウンドを用い、バッチ式インターナ
ルミキサーで混練したのち、該ゴムコンパウンド100
重量部に対し、粉砕媒体としてのロックウール繊維(ア
サノCMF;日本セメント社製、平均繊維径5μm、平
均繊維長さ7mm)を185重量部、及び液状防着剤と
してのシリコーンオイル(KF96−50CS:信越化
学工業社製)を3.0重量部の割合に添加し、加圧型ニ
ーダーを用いて混練粉砕した。得られたゴム粉末100
重量部に対し、粉末再付着を防止するため、固体防着剤
としてのシリカ粉末(カープレックス67;塩野義製薬
社製)を6.2重量部の割合に添加してスーパーミキサ
ーで混合し、次いで60メッシュの篩で分級して平均粒
径75μm、加硫後の硬度(ショアーA)87度、比重
1.8の未加硫ゴム粉末を得た。To produce the elastic powder, a rubber compound having the same composition as in Example 1 was used, and after kneading with a batch type internal mixer, the rubber compound 100 was used.
185 parts by weight of rockwool fiber (Asano CMF; manufactured by Nippon Cement Co., Ltd., average fiber diameter 5 μm, average fiber length 7 mm) as a grinding medium, and silicone oil (KF96-50CS as a liquid anti-adhesive agent) per part by weight. (Manufactured by Shin-Etsu Chemical Co., Ltd.) in an amount of 3.0 parts by weight, and kneaded and pulverized using a pressure kneader. Obtained rubber powder 100
In order to prevent powder re-adhesion, silica powder (Carplex 67; manufactured by Shionogi Pharmaceutical Co., Ltd.) as a solid anti-adhesive agent is added to a weight ratio of 6.2 parts by weight and mixed with a super mixer, Then, classification was carried out with a 60-mesh sieve to obtain an unvulcanized rubber powder having an average particle size of 75 μm, a hardness (Shore A) after vulcanization of 87 degrees, and a specific gravity of 1.8.
【0044】そして、表3に示す抄紙材料の配合割合に
て、実施例1の抄紙工程と同様にして抄紙操作を行い、
それぞれ配合を異にした4種類の抄造紙(3)、
(4)、(5)、(6)を作製した。抄造紙(3)〜
(6)の目付重量は、いずれも700g/m2 とした。Then, a papermaking operation was carried out in the same manner as in the papermaking process of Example 1 with the mixing ratios of the papermaking materials shown in Table 3.
4 types of papermaking paper (3) with different formulations,
(4), (5) and (6) were produced. Papermaking paper (3)
The weight per unit area (6) was 700 g / m 2 .
【0045】[0045]
【表3】 そして、上記により得られた各種抄造紙(3)〜(6)
を、図2〜5に示す各種の態様に重ね、かつ上下両面に
表層材(11)(11)を重ねて実施例1と同じ方法に
より積層一体化して、試料No. 2〜5の成形プレス用ク
ッション材を得た。[Table 3] And the various papermaking papers (3) to (6) obtained as described above
2-5, and the surface layer materials (11) and (11) are layered on both upper and lower surfaces and laminated and integrated by the same method as in Example 1, and the molding presses of Sample Nos. 2 to 5 are laminated. I got a cushion material.
【0046】実施例3 この実施例は、弾性体粉末として、混練粉砕の方法によ
って微細化したふっ素ゴムからなるゴム粉末を用いたも
のである。Example 3 In this example, as the elastic powder, a rubber powder made of fluororubber finely divided by the method of kneading and pulverization was used.
【0047】このゴム粉末は、そのゴムコンパウンドに
下記表4の配合組成のものを用いた。As the rubber powder, the rubber compound having the compounding composition shown in Table 4 below was used.
【0048】[0048]
【表4】 上記ゴムコンパウンドを用い、粉砕媒体、液状防着剤を
下記表5の割合に添加配合して、実施例2と同様の操作
により混練粉砕し、更に固体防着剤を添加して混合した
後分級し、平均粒径75μm、加硫後のショアーA硬度
92度、比重2.5の未加硫ゴム粉末を作製した。[Table 4] Using the above rubber compound, a pulverizing medium and a liquid anti-adhesive agent were added and blended in the proportions shown in Table 5 below, and kneaded and pulverized in the same manner as in Example 2, and a solid anti-adhesive agent was further added and mixed, followed by classification. Then, an unvulcanized rubber powder having an average particle size of 75 μm, a Shore A hardness after vulcanization of 92 degrees, and a specific gravity of 2.5 was produced.
【0049】[0049]
【表5】 そして、表6に示す抄紙材料の配合割合にて、実施例1
の抄紙工程と同様にして抄紙操作を行い、それぞれ配合
を異にした2種類の抄造紙(7)、(8)を作製した。
抄造紙(7)、(8)の目付重量は、いずれも700g
/m2 とした。[Table 5] Then, in the mixing ratio of the papermaking material shown in Table 6, Example 1
A papermaking operation was performed in the same manner as in the papermaking process of No. 2, and two types of papermaking papers (7) and (8) having different formulations were produced.
The weight per unit area of papermaking papers (7) and (8) is 700 g.
/ M 2 .
【表6】 そして、上記により得られた2種類の抄造紙(7)、
(8)を、図6に示す態様に重ね、かつ上下両面に表層
材(11)(11)を重ねて実施例1と同じ方法により
積層一体化して、試料No. 6の成形プレス用クッション
材を得た。[Table 6] Then, the two types of papermaking paper (7) obtained above,
Cushion material for sample press of Sample No. 6 was prepared by stacking (8) in the manner shown in FIG. 6 and stacking surface layer materials (11) and (11) on both upper and lower surfaces and stacking and integrating them by the same method as in Example 1. Got
【0050】実施例4 この実施例は、弾性体粉末として、EDPMからなり、
粉砕媒体として中空ガラスビーズを用いて混練粉砕した
ゴム粉末を用いたものである。Example 4 This example consists of EDPM as elastic powder,
A rubber powder obtained by kneading and pulverizing hollow glass beads as a pulverizing medium is used.
【0051】ゴム粉末は、そのコンパウンドに下記表7
の配合組成のものを用いた。The rubber powder was added to the compound as shown in Table 7 below.
The compounding composition of was used.
【0052】[0052]
【表7】 上記ゴムコンパウンドを用い、粉砕媒体、液状防着剤を
下記表8の割合に添加配合して、実施例2と同様の操作
により混練粉砕し、更に固体防着剤を添加して混合した
後分級し、平均粒径75μm、加硫後のショアーA硬度
85度、比重1.2の未加硫ゴム粉末を作製した。[Table 7] Using the above rubber compound, a pulverizing medium and a liquid anti-adhesive agent were added and blended in the proportions shown in Table 8 below, and kneaded and pulverized in the same manner as in Example 2, and a solid anti-adhesive agent was further added and mixed, followed by classification. Then, an unvulcanized rubber powder having an average particle diameter of 75 μm, Shore A hardness after vulcanization of 85 degrees and a specific gravity of 1.2 was produced.
【0053】[0053]
【表8】 そして、表9に示す抄紙材料の配合割合にて、実施例1
の抄紙工程と同様にして抄紙操作を行い、それぞれ配合
を異にした2種類の抄造紙(9)、(10)を作製し
た。抄造紙(9)の目付重量は700g/m2 、抄造紙
(10)の目付重量は400g/m2 とした。[Table 8] Then, in the mixing ratio of the papermaking material shown in Table 9, Example 1
A papermaking operation was performed in the same manner as in the papermaking process of No. 2, and two types of papermaking papers (9) and (10) having different formulations were produced. The weight per unit area of the papermaking paper (9) was 700 g / m 2 , and the weight per unit area of the papermaking paper (10) was 400 g / m 2 .
【0054】[0054]
【表9】 そして、上記により得られた2種類の抄造紙(9)、
(10)を、図7に示す各種の態様に重ね、かつ上下両
面に表層材(11)(11)を重ねて実施例1と同じ方
法により積層一体化して、試料No. 7の成形プレス用ク
ッション材を得た。[Table 9] Then, the two types of papermaking paper (9) obtained above,
(10) was overlaid on the various aspects shown in FIG. 7, and the surface layer materials (11) and (11) were overlaid on both upper and lower surfaces and laminated and integrated by the same method as in Example 1, for the molding press of Sample No. 7. I got a cushion material.
【0055】(比較例1)芳香族ポリアミド繊維の紡績
糸による目付重量130g/m2 の基布4層と、2d
(600重量%)及び5d(40重量%)の芳香族ポリ
アミド繊維からなる目付重量350g/m2 のパット5
層とを交互に積層して、パット5層、基布4層からなる
積層物とし、これらをニードルパンチングにより結合一
体化した。そして、180℃、20kg/cm2 のプレ
スに70分間かけて、目付重量2270g/cm2 の不
織布製成形プレス用クッション材を得た。これを試料N
o. 8とした。(Comparative Example 1) Four layers of base fabric having a basis weight of 130 g / m 2 made of spun yarn of aromatic polyamide fiber and 2d
(600% by weight) and 5d (40% by weight) of aromatic polyamide fiber, Pat 5 having a basis weight of 350 g / m 2 .
The layers were alternately laminated to form a laminate consisting of 5 layers of pad and 4 layers of base cloth, which were united and integrated by needle punching. Then, it was subjected to a press at 180 ° C. and a pressure of 20 kg / cm 2 for 70 minutes to obtain a non-woven fabric forming press cushion material having a basis weight of 2270 g / cm 2 . This is sample N
o.8.
【0056】(比較例2)濾水値200秒に調整した耐
熱性芳香族系重合体(ポリメタフェニレンイソフタルア
ミド)のパルプ状物質20体積部と、平均繊維長150
μm、繊維太さ4.1μmの微細ロックウール繊維80
体積部を混合し、固形分濃度1%の水分散液を調整し
た。これを円網抄紙機にて湿紙に抄造してフェルトに転
移し、脱水して水分含有率80%とした。更にこのよう
にして得た湿紙をメーキングドラムに70枚積層し、つ
いで35kg/cm2 ,140℃のホットプレスにて圧
搾、乾燥し、目付重量2,800g/m2 、厚さ2.4
mmのボード状の抄紙型成形プレス用クッション材を得
た。これを試料No. 9とした。Comparative Example 2 20 parts by volume of a pulp-like substance of a heat-resistant aromatic polymer (polymetaphenylene isophthalamide) adjusted to a drainage value of 200 seconds and an average fiber length of 150
80 μm fine rockwool fiber with a thickness of 4.1 μm
Volume parts were mixed to prepare an aqueous dispersion having a solid content concentration of 1%. This was made into wet paper with a cylinder paper machine, transferred to felt, and dehydrated to a water content of 80%. Further, 70 sheets of the wet paper thus obtained were laminated on a making drum, then squeezed by a hot press of 35 kg / cm 2 and 140 ° C. and dried to have a basis weight of 2,800 g / m 2 and a thickness of 2.4.
A board-shaped cushioning material for papermaking molding press having a size of mm was obtained. This was designated as Sample No. 9.
【0057】(性能比較試験)上記実施例1〜4で製作
した試料No. 1〜7、及び比較例1〜2で得られた試料
No. 8、9の各成形プレス用クッション材につき、目付
精度の測定を行うと共に、耐久性を調べるためのプレス
試験を行い、プレス試験前後のクッション性の変化、厚
み変化を調べた。(Performance comparison test) Sample Nos. 1 to 7 produced in Examples 1 to 4 and samples obtained in Comparative Examples 1 and 2
With respect to the cushioning materials for forming presses of Nos. 8 and 9, the basis weight accuracy was measured, and a press test for examining durability was performed to examine changes in cushioning properties and thickness changes before and after the press test.
【0058】プレス試験は、圧力30kg/cm2 、加
熱温度180℃で90分間保持し、その後加圧状態を保
持しながら30分間冷却し、ついで3分間除圧解放する
プレスサイクルを200回繰返すことによって行った。In the press test, a pressure cycle of 30 kg / cm 2 and a heating temperature of 180 ° C. was maintained for 90 minutes, followed by cooling for 30 minutes while maintaining a pressurized state, and then depressurized release for 3 minutes. Went by.
【0059】そして、前記目付精度、クッション性、厚
み変化を次の条件で測定した。その結果を下記表10に
示す。Then, the above-mentioned areal accuracy, cushioning property, and thickness change were measured under the following conditions. The results are shown in Table 10 below.
【0060】目付精度 :50mm角のポンチでクッ
ション材を100mmピッチで打ち抜いた打抜き片12
1個について、それぞれの重量を測り、最大重量W1 、
最小重量W2 、平均重量Waとしたとき、(W1 −
W2)/Wa×100の式で求めた。Fabrication accuracy: Punching piece 12 in which a cushion material is punched at a pitch of 100 mm with a punch of 50 mm square.
Each one is weighed and the maximum weight W 1 ,
Assuming that the minimum weight is W 2 and the average weight is Wa, (W 1 −
It was determined by the formula of W 2 ) / Wa × 100.
【0061】クッション性:120℃の温度で8kg/
cm2 の圧力から35kg/cm2 の圧力に増大して圧
縮したときの厚みの変化量を測定した。変化率は、20
0回プレス試験後の厚み変化量T1 、プレス試験前の厚
み変化量T2 としたとき、(T1 −T2 )/T1 ×10
0として求めた。Cushioning property: 8 kg / at a temperature of 120 ° C.
The amount of change in thickness when compressed to increase the pressure of cm 2 to a pressure of 35 kg / cm 2 was measured. The rate of change is 20
0 times press testing thickness change amount T 1 of the post, when the thickness variation T 2 of the previous press test, (T 1 -T 2) / T 1 × 10
It was calculated as 0.
【0062】厚み変化 :常温で、圧力35kg/c
m2 の圧縮時のクッション材の厚みを測定した。変化率
は、上記クッション性の変化率に準じて計算した。Thickness change: Pressure at room temperature, 35 kg / c
The thickness of the cushion material at the time of compression of m 2 was measured. The rate of change was calculated according to the rate of change in the cushioning property.
【0063】[0063]
【表10】 表10に示されるように、比較例1の従来の不織布製ク
ッション材(試料No.8)は、目付精度においてばらつ
きが大きく、クッション性も初期において良好であるも
のゝ、プレス試験後においては大きく低減する。かつ厚
みも使用の繰返しによる低減量が大きく、耐久性に劣
る。[Table 10] As shown in Table 10, the conventional non-woven cushion material of Comparative Example 1 (Sample No. 8) has a large variation in the areal accuracy and a good cushioning property in the initial stage. Reduce. In addition, the thickness is greatly reduced by repeated use, resulting in poor durability.
【0064】一方、比較例2の従来の抄造紙製のクッシ
ョン材(試料No. 9)は、目付精度、厚みの変化率にお
いて良好であるものゝ、クッション性に劣る。On the other hand, the conventional paper-made cushioning material of Comparative Example 2 (Sample No. 9) has a good basis weight accuracy and thickness change rate, but is inferior in cushioning property.
【0065】これらの従来品に対し、本発明による試料
No. 1〜7のクッション材は、いずれも目付精度、クッ
ション性に優れ、しかも該クッション性が繰返し使用後
においても比較的良好に保持される。また、使用による
厚みの変化も少なく、耐久性に優れているものであるこ
とが判る。In contrast to these conventional products, the sample according to the present invention
The cushion materials of Nos. 1 to 7 are all excellent in unit weight accuracy and cushioning property, and the cushioning property is relatively well retained even after repeated use. Further, it can be seen that the change in thickness due to use is small and the durability is excellent.
【0066】[0066]
【発明の効果】この発明に係るクッション材は、上述の
説明から既に明らかなように、厚み分布が均一で目付精
度に優れ、厚みの経時的変化が少なく、しかも良好なク
ッション性を保有し、かつ圧縮復元力に優れていて耐用
寿命の顕著な増大をはかることができる効果を奏する。As is apparent from the above description, the cushioning material according to the present invention has a uniform thickness distribution, excellent basis weight accuracy, little change in thickness over time, and good cushioning properties. In addition, it has an excellent compressive and restoring force, and has an effect that the useful life can be remarkably increased.
【0067】また、この発明に係るクッション材の製造
方法によれば、均一に微細化された弾性体粉末を容易
に、かつ高い収率で製造し、該弾性体粉末を抄造紙中に
均一に分散させることができるので、上記諸特性に最も
優れたクッション材を効率良く製造することができる。Further, according to the method for producing a cushioning material of the present invention, uniformly finely divided elastic powder can be produced easily and at a high yield, and the elastic powder can be uniformly dispersed in the papermaking paper. Since it can be dispersed, it is possible to efficiently manufacture the cushioning material having the best characteristics described above.
【図1】実施例1によって製造されるクッション材の構
成図である。FIG. 1 is a configuration diagram of a cushion material manufactured according to a first embodiment.
【図2】実施例2によって製造されるクッション材の1
つの構成図である。FIG. 2 is one of cushion materials manufactured by Example 2;
It is one block diagram.
【図3】実施例2によって製造されるクッション材の他
の1つの構成図である。FIG. 3 is another configuration diagram of the cushioning material manufactured according to the second embodiment.
【図4】実施例2によって製造されるクッション材の更
に他の1つの構成図である。FIG. 4 is still another configuration diagram of the cushioning material manufactured according to the second embodiment.
【図5】実施例2によって製造されるクッション材の更
に他の1つの構成図である。FIG. 5 is still another configuration diagram of the cushioning material manufactured according to the second embodiment.
【図6】実施例3によって製造されるクッション材の構
成図である。FIG. 6 is a configuration diagram of a cushion material manufactured according to a third embodiment.
【図7】実施例4によって製造されるクッション材の構
成図である。FIG. 7 is a configuration diagram of a cushion material manufactured according to a fourth embodiment.
1〜10…抄造紙 11…表層材 1-10 ... Papermaking paper 11 ... Surface material
─────────────────────────────────────────────────────
─────────────────────────────────────────────────── ───
【手続補正書】[Procedure amendment]
【提出日】平成5年7月22日[Submission date] July 22, 1993
【手続補正1】[Procedure Amendment 1]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0027[Name of item to be corrected] 0027
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0027】混練粉砕に際しては、必要に応じて液状防
着剤が添加される。液状防着剤は、粉砕媒体によって粉
砕された弾性体の切断面に付着し、その再凝着を防止し
て、微粉砕化を促進する作用を果す。かかる液状防着剤
としてはシリコーンオイル、ふっ素オイル等の非水系界
面活性剤、または水溶性界面活性剤が用いられる。その
添加量は、弾性体コンパウンド100重量部に対し、3
重量部以下とすべきである。3重量部をこえて過多に用
いると、抄造時に泡立ち等の悪影響を与えるのみなら
ず、抄造後の紙の使用中に防着剤が滲出するおそれがあ
る。At the time of kneading and pulverization, a liquid anti-adhesive agent is added if necessary. The liquid anti-adhesive agent adheres to the cut surface of the elastic body crushed by the crushing medium, prevents re-adhesion of the elastic body, and promotes fine pulverization. As the liquid anti-adhesive agent, a non-aqueous surfactant such as silicone oil or fluorine oil, or a water-soluble surfactant is used. The amount added to the elastic member Konpaun de 1 00 parts by weight, 3
It should be less than or equal to parts by weight. If it is used in excess of 3 parts by weight, not only adverse effects such as foaming may occur at the time of papermaking but also the anti-adhesion agent may exude during use of the paper after papermaking.
【手続補正2】[Procedure Amendment 2]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0039[Correction target item name] 0039
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0039】[0039]
【表1】 次いで、次のようにして抄紙を行った。先ず、ビーター
を用いて、ロックウール繊維(平均繊維径5μm、平均
繊維長7mm)を多量の水とともに離解し、繊維を水中
に均一に分散させたのち、フィブリル化した芳香族ポリ
アミドからなるパルプ状物質を加え、同様に分散させ
た。そして、これに上記弾性体粉末と分散剤とを加えて
同様に分散させ、得られた一次スラリーをパルパーに投
入し、ラテックス系のバインダーを加えて最終離解を行
った。そしてこのスラリーをチェストに投入し、水を加
えて濃度調整を行うと共に、凝集剤を加えてフロック調
整を行って最終スラリーとしたのち、このスラリーを長
網抄紙機のワイヤー上に流し込んで湿紙を形成し、脱
水、乾燥させて目付重量700g/m2 の抄造紙を製作
した。[Table 1] Then, papermaking was performed as follows. First, using a beater, rockwool fibers (average fiber diameter 5 μm, average fiber length 7 mm) were disintegrated together with a large amount of water, and the fibers were uniformly dispersed in the water, and then pulped from fibrillated aromatic polyamide. Material was added and similarly dispersed. Then, the elastic powder and the dispersant were added to and dispersed in the same manner, and the obtained primary slurry was put into a pulper, and a latex binder was added to perform final disaggregation. Then, this slurry is put into a chest, water is added to adjust the concentration, and a flocculant is added to adjust the flocs to obtain a final slurry, which is then poured onto a wire of a Fourdrinier paper machine to obtain a wet paper web. Was formed, dehydrated and dried to produce a papermaking paper having a basis weight of 700 g / m 2 .
【手続補正3】[Procedure 3]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0049[Correction target item name] 0049
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0049】[0049]
【表5】 そして、表6に示す抄紙材料の配合割合にて、実施例1
の抄紙工程と同様にして抄紙操作を行い、それぞれ配合
を異にした2種類の抄造紙(7)、(8)を作製した。
抄造紙(7)、(8)の目付重量は、いずれも700g
/m2 とした。[Table 5] Then, in the mixing ratio of the papermaking material shown in Table 6, Example 1
A papermaking operation was performed in the same manner as in the papermaking process of No. 2, and two types of papermaking papers (7) and (8) having different formulations were produced.
The weight per unit area of papermaking papers (7) and (8) is 700 g.
/ M 2 .
【手続補正4】[Procedure amendment 4]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0052[Correction target item name] 0052
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0052】[0052]
【表7】 上記ゴムコンパウンドを用い、粉砕媒体、液状防着剤を
下記表8の割合に添加配合して、実施例2と同様の操作
により混練粉砕し、更に固体防着剤を添加して混合した
後分級し、平均粒径75μm、加硫後のショアーA硬度
85度、比重1.2の未加硫ゴム粉末を作製した。[Table 7] Using the above rubber compound, a pulverizing medium and a liquid anti-adhesive agent were added and blended in the proportions shown in Table 8 below, and kneaded and pulverized in the same manner as in Example 2, and a solid anti-adhesive agent was further added and mixed, followed by classification. Then, an unvulcanized rubber powder having an average particle diameter of 75 μm, Shore A hardness after vulcanization of 85 degrees and a specific gravity of 1.2 was produced.
【手続補正5】[Procedure Amendment 5]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0053[Correction target item name] 0053
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0053】[0053]
【表8】 そして、表9に示す抄紙材料の配合割合にて、実施例1
の抄紙工程と同様にして抄紙操作を行い、それぞれ配合
を異にした2種類の抄造紙(9)、(10)を作製し
た。抄造紙(9)の目付重量は700g/m2 、抄造紙
(10)の目付重量は400g/m2 とした。[Table 8] Then, in the mixing ratio of the papermaking material shown in Table 9, Example 1
A papermaking operation was performed in the same manner as in the papermaking process of No. 2, and two types of papermaking papers (9) and (10) having different formulations were produced. The weight per unit area of the papermaking paper (9) was 700 g / m 2 , and the weight per unit area of the papermaking paper (10) was 400 g / m 2 .
【手続補正6】[Procedure correction 6]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0054[Correction target item name] 0054
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0054】[0054]
【表9】 そして、上記により得られた2種類の抄造紙(9)、
(10)を、図7に示す各種の態様に重ね、かつ上下両
面に表層材(11)(11)を重ねて実施例1と同じ方
法により積層一体化して、試料No. 7の成形プレス用ク
ッション材を得た。[Table 9] Then, the two types of papermaking paper (9) obtained above,
(10) was overlaid on the various aspects shown in FIG. 7, and the surface layer materials (11) and (11) were overlaid on both upper and lower surfaces and laminated and integrated by the same method as in Example 1, for the molding press of Sample No. 7. I got a cushion material.
【手続補正7】[Procedure Amendment 7]
【補正対象書類名】明細書[Document name to be amended] Statement
【補正対象項目名】0055[Correction target item name] 0055
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【0055】(比較例1)芳香族ポリアミド繊維の紡績
糸による目付重量130g/m2 の基布4層と、2d
(600重量%)及び5d(40重量%)の芳香族ポリ
アミド繊維からなる目付重量350g/m2 のバット5
層とを交互に積層して、バット5層、基布4層からなる
積層物とし、これらをニードルパンチングにより結合一
体化した。そして、180℃、20kg/cm2 のプレ
スに70分間かけて、目付重量2270g/cm2 の不
織布製成形プレス用クッション材を得た。これを試料N
o. 8とした。(Comparative Example 1) Four layers of base fabric having a basis weight of 130 g / m 2 made of spun yarn of aromatic polyamide fiber and 2d
(600 wt%) and 5d aromatic Bas Tsu bets 5 having a basis weight 350 g / m 2 consisting of polyamide fibers (40 wt%)
By laminating a layer alternately, bar Tsu bets five layers, a laminate consisting of the base fabric 4 layers and these combined integrated by needle punching. Then, it was subjected to a press at 180 ° C. and a pressure of 20 kg / cm 2 for 70 minutes to obtain a non-woven fabric forming press cushion material having a basis weight of 2270 g / cm 2 . This is sample N
o.8.
【手続補正8】[Procedure Amendment 8]
【補正対象書類名】図面[Document name to be corrected] Drawing
【補正対象項目名】図4[Name of item to be corrected] Fig. 4
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【図4】 [Figure 4]
【手続補正9】[Procedure Amendment 9]
【補正対象書類名】図面[Document name to be corrected] Drawing
【補正対象項目名】図5[Name of item to be corrected] Figure 5
【補正方法】変更[Correction method] Change
【補正内容】[Correction content]
【図5】 [Figure 5]
Claims (11)
性体粉末とを主成分として含み、上記弾性体粉末が全体
に均一に分散含有された抄造紙からなることを特徴とす
る成形プレス用クッション材。1. A cushion for a molding press, comprising a papermaking paper containing organic fibers and / or inorganic fibers as main components and elastic powder as main components, and the elastic powder being uniformly dispersed and contained throughout. Material.
/または無機繊維と、弾性体粉末のほかに、更に高分子
パルプ状物質を含むことを特徴とする請求項1記載の成
形プレス用クッション材。2. The cushion for a molding press according to claim 1, characterized in that, in addition to the organic fiber and / or the inorganic fiber and the elastic powder as a main component of the papermaking paper, a polymer pulp-like substance is further contained. Material.
/または無機繊維と、弾性体粉末のほかに、更にバイン
ダーを含む請求項1記載の成形プレス用クッション材。3. The cushioning material for forming press according to claim 1, which further comprises a binder in addition to the organic fiber and / or the inorganic fiber, the elastic body powder, as a main component of the papermaking paper.
/または無機繊維と、弾性体粉末のほかに、更に高分子
パルプ状物質と、バインダーとを含むことを特徴とする
請求項1記載の成形プレス用クッション材。4. The main component of the papermaking paper, in addition to the organic fiber and / or the inorganic fiber, the elastic body powder, a polymer pulp-like substance and a binder are further contained. Cushion material for molding press.
層材が貼着一体化されてなる請求項1ないし4のいずれ
か1に記載の成形プレス用クッション材。5. The cushion material for a molding press according to claim 1, wherein a releasable surface layer material is stuck and integrated on both surfaces of the cushion material substrate.
m、繊維長300〜15,000μmである請求項1な
いし5のいずれか1に記載の成形プレス用クッション
材。6. The organic and inorganic fibers have a fiber diameter of 1 to 30 μm.
The cushioning material for a molding press according to any one of claims 1 to 5, having a fiber length of m and a fiber length of 300 to 15,000 µm.
μmである請求項1ないし6のいずれか1に記載の成形
プレス用クッション材。7. The elastic powder has an average particle diameter of 20 to 250.
The cushioning material for forming press according to any one of claims 1 to 6, which has a thickness of μm.
JIS A硬度20〜98度である請求項1ないし7の
いずれか1に記載の成形プレス用クッション材。8. The elastic powder has a hardness after vulcanization,
The cushion material for a molding press according to any one of claims 1 to 7, which has a JIS A hardness of 20 to 98 degrees.
分子パルプ状物質と、弾性体粉末との3者を合わせた体
積に対して、弾性体粉末の配合量が10〜95%に設定
されてなる請求項1ないし8のいずれか1に記載の成形
プレス用クッション材。9. The content of the elastic powder is set to 10 to 95% with respect to the combined volume of the organic fiber and / or the inorganic fiber, the polymer pulp-like substance and the elastic powder. The cushioning material for molding press according to any one of claims 1 to 8.
繊維状の固形粉砕媒体を加えて混練粉砕することにより
平均粒子径250μm以下の弾性体粉末を作製し、 該弾性体粉末を、少なくとも有機繊維および/または無
機繊維を含む抄造紙材料を離解した水性スラリーに分散
させ、 該水性スラリーから前記弾性体粉末が内部に均一に分散
した抄造紙に抄造することを特徴とする成形プレス用ク
ッション材の製造方法。10. An elastic powder having an average particle diameter of 250 μm or less is produced by adding a granular or fibrous solid pulverizing medium to the elastic compound and kneading and pulverizing the elastic powder. Production of a cushioning material for forming press, characterized in that a papermaking material containing inorganic fibers / or inorganic fibers is dispersed in a disaggregated aqueous slurry, and papermaking is made from the aqueous slurry into a papermaking paper in which the elastic powder is uniformly dispersed inside. Method.
100重量部に対し、粉砕媒体を40〜400重量部の
割合に配合する請求項10記載の成形プレス用クッショ
ン材の製造方法。11. The method for producing a cushioning material for a molding press according to claim 10, wherein, when kneading and pulverizing, the pulverizing medium is mixed in a proportion of 40 to 400 parts by weight with respect to 100 parts by weight of the elastic compound.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5168113A JP2535129B2 (en) | 1993-07-07 | 1993-07-07 | Cushion material for molding press and method of manufacturing the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5168113A JP2535129B2 (en) | 1993-07-07 | 1993-07-07 | Cushion material for molding press and method of manufacturing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH07229097A true JPH07229097A (en) | 1995-08-29 |
| JP2535129B2 JP2535129B2 (en) | 1996-09-18 |
Family
ID=15862100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5168113A Expired - Fee Related JP2535129B2 (en) | 1993-07-07 | 1993-07-07 | Cushion material for molding press and method of manufacturing the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2535129B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005108674A1 (en) * | 2004-05-07 | 2005-11-17 | Kao Corporation | Article formed into sheet, method for producing the same and exothermic formed article |
| WO2008010363A1 (en) * | 2006-07-18 | 2008-01-24 | Yamauchi Corporation | Cushioning material for heat press and method for producing the same |
| JP2013001764A (en) * | 2011-06-14 | 2013-01-07 | Sumitomo Bakelite Co Ltd | Fiber-resin composite structure, method for producing molded body, and molded body |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102830716B1 (en) * | 2023-04-28 | 2025-07-08 | 주식회사 쓰리디팩토리 | Press mold and its production method |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1263812A (en) * | 1969-08-27 | 1972-02-16 | Wiggins Teape Res Dev | A method of forming fibrous sheet material |
| JPS5224122A (en) * | 1975-08-20 | 1977-02-23 | Kato Asamichi | Method of making mold of good disintegrating property |
| JPS6360715A (en) * | 1986-09-01 | 1988-03-16 | Mitsubishi Paper Mills Ltd | Heat-resistant cushion material for molding press |
| JPH0260799A (en) * | 1988-08-26 | 1990-03-01 | Takara Co Ltd | Decorative object using optical fiber |
-
1993
- 1993-07-07 JP JP5168113A patent/JP2535129B2/en not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1263812A (en) * | 1969-08-27 | 1972-02-16 | Wiggins Teape Res Dev | A method of forming fibrous sheet material |
| JPS5224122A (en) * | 1975-08-20 | 1977-02-23 | Kato Asamichi | Method of making mold of good disintegrating property |
| JPS6360715A (en) * | 1986-09-01 | 1988-03-16 | Mitsubishi Paper Mills Ltd | Heat-resistant cushion material for molding press |
| JPH0260799A (en) * | 1988-08-26 | 1990-03-01 | Takara Co Ltd | Decorative object using optical fiber |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005108674A1 (en) * | 2004-05-07 | 2005-11-17 | Kao Corporation | Article formed into sheet, method for producing the same and exothermic formed article |
| US8084139B2 (en) | 2004-05-07 | 2011-12-27 | Kao Corporation | Article formed into sheet, method for producing the same and exothermic formed article |
| WO2008010363A1 (en) * | 2006-07-18 | 2008-01-24 | Yamauchi Corporation | Cushioning material for heat press and method for producing the same |
| JP2008023749A (en) * | 2006-07-18 | 2008-02-07 | Yamauchi Corp | Cushioning material for heat press and its manufacturing method |
| US8709590B2 (en) | 2006-07-18 | 2014-04-29 | Yamauchi Corporation | Hot-press cushion material and manufacturing method of the same |
| JP2013001764A (en) * | 2011-06-14 | 2013-01-07 | Sumitomo Bakelite Co Ltd | Fiber-resin composite structure, method for producing molded body, and molded body |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2535129B2 (en) | 1996-09-18 |
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