JPH01139253A - Production of dust-arresting integrated mat - Google Patents
Production of dust-arresting integrated matInfo
- Publication number
- JPH01139253A JPH01139253A JP29610787A JP29610787A JPH01139253A JP H01139253 A JPH01139253 A JP H01139253A JP 29610787 A JP29610787 A JP 29610787A JP 29610787 A JP29610787 A JP 29610787A JP H01139253 A JPH01139253 A JP H01139253A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- precoat layer
- rubber sheet
- unvulcanized
- vulcanization
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 229920001971 elastomer Polymers 0.000 claims abstract description 58
- 239000005060 rubber Substances 0.000 claims abstract description 55
- 238000004073 vulcanization Methods 0.000 claims abstract description 24
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 22
- 239000000463 material Substances 0.000 claims abstract description 22
- 229920000126 latex Polymers 0.000 claims abstract description 17
- 239000000835 fiber Substances 0.000 claims description 10
- 239000000428 dust Substances 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 239000005062 Polybutadiene Substances 0.000 claims description 2
- 229920002857 polybutadiene Polymers 0.000 claims description 2
- 239000004636 vulcanized rubber Substances 0.000 claims description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims 2
- 229910002092 carbon dioxide Inorganic materials 0.000 claims 1
- 239000001569 carbon dioxide Substances 0.000 claims 1
- 125000002560 nitrile group Chemical group 0.000 claims 1
- 239000004744 fabric Substances 0.000 abstract description 10
- 238000004140 cleaning Methods 0.000 abstract description 5
- 230000008929 regeneration Effects 0.000 abstract description 4
- 238000011069 regeneration method Methods 0.000 abstract description 4
- 238000010438 heat treatment Methods 0.000 abstract description 3
- 238000003825 pressing Methods 0.000 abstract description 3
- 230000010354 integration Effects 0.000 abstract 1
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- -1 quinonedioxime thiol Chemical class 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- QWEWLLNSJDTOKH-UHFFFAOYSA-N 1,3-thiazole-2-carboxamide Chemical class NC(=O)C1=NC=CS1 QWEWLLNSJDTOKH-UHFFFAOYSA-N 0.000 description 1
- WGJCBBASTRWVJL-UHFFFAOYSA-N 1,3-thiazolidine-2-thione Chemical compound SC1=NCCS1 WGJCBBASTRWVJL-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 description 1
- 229960002089 ferrous chloride Drugs 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 229920002681 hypalon Polymers 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical class [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 150000003549 thiazolines Chemical class 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical class CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
Landscapes
- Lining Or Joining Of Plastics Or The Like (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は除應用一体化マットの製法に関するものであり
、より詳細には、ゴム接着性の繊維はもとより、ゴム非
接着性の合成繊維を含むパイル糸をも安定して、且つ良
好に接着可能で、洗浄及び再生処理を反復して長期間に
わたって使用する際にも、波打ちの発生が防止され寸法
安定性が顕著に向上した除塵用一体止マットの製法に関
する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for producing an integrated mat for de-escorting, and more specifically, the present invention relates to a method for manufacturing an integrated mat for de-escorting. A dust-removal integrated product that can stably and well adhere even pile yarns, prevents the occurrence of waviness, and has significantly improved dimensional stability even when used for long periods of time after repeated cleaning and recycling treatments. Regarding the manufacturing method of stop mats.
(従来の技術)
従来、玄関等の出入口等に敷設して使用される除塵用一
体止マットとして、タフト化マットのバックステッチ面
にゴム及び塩化ビニルシートを一体化させたものがよく
知られている。(Prior Art) Conventionally, as an integrated dust removal mat that is used by laying at entrances and exits of entrances, etc., it is well known that a tufted mat with rubber and vinyl chloride sheets integrated into the backstitched surface is used. There is.
この一体止マットは塩化ビニル等の軟質樹脂をゾル状で
マットの繊維部(基布及びパイル)と接着させ、熱処理
を行って固化させる方法や、未加硫のゴムシート上にマ
ット繊維部をのせた後、熱プレス処理を行って接着固化
させる方法で製造されていた。This one-piece mat can be produced by bonding a soft resin such as vinyl chloride to the fibers of the mat (base fabric and pile) in sol form and then heat-treating to harden it, or by attaching the fibers of the mat to an unvulcanized rubber sheet. It was manufactured by applying a heat press treatment to bond and solidify the adhesive.
また特開昭59−95016号のように、マット材料の
ステッチ面にエラストマーを塗布して薄いバッキング層
を成形し、枠状の厚いエラストマーを一体化するという
方法がある。There is also a method, as disclosed in JP-A-59-95016, in which an elastomer is applied to the stitched surface of a mat material to form a thin backing layer, and a frame-shaped thick elastomer is integrated.
(発明が解決しようとする問題点)
これらの一体止マットは、人の出入口等に敷設されるも
のであるから、パイ”ル面は靴の裏面による摩擦を繰返
し受ける。更に該マットは一定期間使用後、これを洗浄
再生し、再び貸与するというレンタルシステムで用いら
れているため、上記のような摩擦や洗浄処理を繰返し受
けることにより、マット材料の伸縮によるマットの波打
ちが生じるという欠点がある。また、パイル糸のマット
からの脱落を生じてマットの所謂痩せを生じることも問
題であり、特に風合い及び耐久性に優れているポリビニ
ルアルコール繊維やポリエステル繊維等ではゴムとの接
着性が悪いため、この傾向が特に大であった。(Problems to be Solved by the Invention) Since these fixed mats are placed at entrances and exits for people, the pile surface is repeatedly subjected to friction from the soles of shoes.Furthermore, the mats are used for a certain period of time. Since it is used in a rental system where the mat is washed and recycled after use and rented out again, it has the disadvantage that the mat material becomes wavy due to expansion and contraction due to repeated friction and washing processes as described above. Another problem is that the pile threads fall off the mat, resulting in so-called thinning of the mat.In particular, polyvinyl alcohol fibers and polyester fibers, which have excellent texture and durability, have poor adhesion to rubber. , this tendency was particularly strong.
従って、本発明の目的は、パイル糸をゴムバラ。Therefore, the object of the present invention is to make the pile yarn elastic.
キングに強固に接着固定することにより、洗浄再生を反
復した場合にも、パイル糸の脱落や波打ちの発生が防止
されると共に寸法安定性が顕著に向上した除塵用一体止
マットの製法を提供するにある。To provide a method for producing an integral fixing mat for dust removal, which prevents pile threads from falling off and waving even when washed and regenerated repeatedly, and has significantly improved dimensional stability, by firmly adhering and fixing the mat to a king. It is in.
(問題点を解決するための手段)
本発明によれば、基材と、該基材にタフト化されたパイ
ルとから成るマット材料のステッチ面にゴム固形分当り
0.1乃至3重量%の加硫剤及び適量の加硫促進剤を含
有するゴムラテックスを塗布して、該ステッチ面に未加
硫乃至半加硫のゴムプレコート層を形成させ、該プレコ
ートマット材料と、プレコート層と同種のゴム、0.1
乃至3重量%の加硫剤及び適量の加硫促進剤を含有する
未加硫ゴムシートとを、該プレコート層とゴムシートと
が対面するように重ね合せて、加熱下にプレスし、該プ
レコート層とゴムシートとの接着と、プレコート層及び
ゴムシートの加硫とを行うことを特徴とする除塵用一体
止マットの製法が提供される。(Means for Solving the Problems) According to the present invention, 0.1 to 3 wt. Rubber latex containing a vulcanizing agent and an appropriate amount of vulcanization accelerator is applied to form an unvulcanized or semi-vulcanized rubber precoat layer on the stitched surface, and the precoat mat material and the same type of precoat layer are coated. Rubber, 0.1
An unvulcanized rubber sheet containing 3 to 3% by weight of a vulcanizing agent and an appropriate amount of a vulcanization accelerator is stacked so that the precoat layer and the rubber sheet face each other, and pressed under heat to form the precoat. Provided is a method for producing an integral mat for dust removal, which is characterized by adhering a layer and a rubber sheet, and vulcanizing a precoat layer and a rubber sheet.
(作用)
本発明によれば、加硫剤を含有するゴムラテックスを未
加硫乃至半加硫の状態でマット材料のステッチ面にプレ
コート層として設ける。これによりマット材料に予じめ
ゴム成分を浸透させておくことが可能となり、しかも後
で施こすゴムシートとの強固な接着一体止が可能となる
。また、後で施こすゴムシートはプレコート層と同種の
ゴム、加硫剤及び加硫促進剤を含有するものであり、加
熱下にプレコートマット材料とゴムシートとをプレスす
ることにより、ゴムプレコート層とゴムシートとが同時
に加硫接着される。(Function) According to the present invention, rubber latex containing a vulcanizing agent is provided as a precoat layer on the stitched surface of the mat material in an unvulcanized or semi-vulcanized state. This makes it possible to infiltrate the rubber component into the mat material in advance, and also allows for strong adhesion to the rubber sheet that will be applied later. In addition, the rubber sheet to be applied later contains the same kind of rubber, vulcanizing agent, and vulcanization accelerator as the pre-coat layer, and by pressing the pre-coat mat material and the rubber sheet under heating, the rubber pre-coat layer is formed. and the rubber sheet are simultaneously vulcanized and bonded.
マット材料とゴムシートとの界面に残菌で寸法安定性及
び耐久性のある接着構造を導入するためには、マット材
料中にゴム成分が浸透し好ましくは投錨効果を有してい
ることと、ゴム自体に強固な架橋構造(加硫構造)が導
入されていることとの両方が必要である。In order to introduce a dimensionally stable and durable adhesive structure with residual bacteria at the interface between the mat material and the rubber sheet, the rubber component must penetrate into the mat material and preferably have an anchoring effect; It is also necessary that a strong crosslinked structure (vulcanized structure) be introduced into the rubber itself.
本発明によればプレコート層を未加硫乃至半加硫の状態
で設け、これに未加硫のゴムシートを加熱下にプレスせ
しめて両者の一体化と加硫とを同時に行うことにより、
パイル糸が十分に固定され、パイル糸の脱落、原布の剥
離、波うち発生が防止できる。According to the present invention, the precoat layer is provided in an unvulcanized or semi-vulcanized state, and an unvulcanized rubber sheet is pressed onto it under heat to simultaneously integrate and vulcanize the two.
The pile yarn is sufficiently fixed, preventing the pile yarn from falling off, the raw fabric from peeling off, and causing waves.
(発明の好適な態様)
本発明の除塵用一体止マットの製造工程を説明する第1
図の工程Aにおいて、基布1にはパイル糸2がタフト化
され且つその先端が切揃えられてマット面を形成してい
るマット材料を用意する。(Preferred embodiment of the invention) A first explanation of the manufacturing process of the integral mat for dust removal of the present invention.
In step A of the figure, a mat material is prepared for the base fabric 1, in which the pile threads 2 are tufted and the ends thereof are trimmed to form a matte surface.
工程Bにおいて基布1の裏面(ステッチ面)に加硫剤及
び加硫促進剤を含有するゴムラテックスを塗布して未加
硫乃至半加硫のプレコート層3を形成させる。工程Cに
おいてプレコートマット材料とプレコート層と同種のゴ
ムを加硫剤及び加硫促進剤を含有する未加硫ゴムシート
4とを、プレコート層3とゴムシート4とが対面するよ
うに重ね合わせ、加熱下にプレスする。In step B, a rubber latex containing a vulcanizing agent and a vulcanization accelerator is applied to the back surface (stitched surface) of the base fabric 1 to form an unvulcanized or semi-vulcanized precoat layer 3. In step C, the precoat mat material and the unvulcanized rubber sheet 4 containing the same type of rubber as the precoat layer, a vulcanizing agent, and a vulcanization accelerator are stacked so that the precoat layer 3 and the rubber sheet 4 face each other, Press under heat.
本発明に用いる基布1としては、アセタール化ポリビニ
ルアルコール繊維、ポリエステル繊維等の寸法安定性に
優れた合成繊維の織布や不織布が使用され、一方パイル
糸2としては、ナイロン繊維、ビニロン繊維、アクリル
繊維等の合成繊維のマルチフィラメント糸、″紡績基或
いはこれらの混紡糸が使用できる他、従来の天然繊維等
も使用することができる。The base fabric 1 used in the present invention is a woven or nonwoven fabric made of synthetic fibers with excellent dimensional stability, such as acetalized polyvinyl alcohol fibers or polyester fibers, while the pile yarn 2 is made of nylon fibers, vinylon fibers, In addition to multifilament yarns of synthetic fibers such as acrylic fibers, spun base yarns, or blended yarns thereof, conventional natural fibers can also be used.
ゴムラテックス、ゴムシートに使用するエラストマーと
しては、ニトリル−ブタジエンゴムが特に好適に使用さ
れるが、加硫可能な他のゴム、例えばスチレンブタジェ
ン共重合体ゴム(5BR) 、クロロブレンゴム、ポリ
ブタジェンゴム、ポリイソプレンゴム、クロロスルフォ
ン化ポリエチレン等を用いることもできる。As the elastomer used for rubber latex and rubber sheets, nitrile-butadiene rubber is particularly preferably used, but other vulcanizable rubbers such as styrene-butadiene copolymer rubber (5BR), chloroprene rubber, polyester rubber, etc. Butadiene rubber, polyisoprene rubber, chlorosulfonated polyethylene, etc. can also be used.
また、ゴムラテックスやゴムシートに配合される加硫剤
としては、無機系加硫剤として、硫黄、塩化亜鉛、塩化
第一鉄、塩化スズ等の金属塩や、塩化硫黄等が挙げられ
、有機過酸化物の加硫剤として、ジクミルペルオキシド
、アセチレンペルオキシド、ベンゾイルペルオキシド、
エチルメチルケトンペルオキシド等が挙げられ、その他
にもチウラミスルフィド、キノンジオキシムチオール、
ジチオ酸等を挙げることができるが、硫黄を用いるのが
普通である。In addition, as vulcanizing agents that are mixed into rubber latex and rubber sheets, inorganic vulcanizing agents include metal salts such as sulfur, zinc chloride, ferrous chloride, and tin chloride, and sulfur chloride. As a peroxide vulcanizing agent, dicumyl peroxide, acetylene peroxide, benzoyl peroxide,
Examples include ethyl methyl ketone peroxide, and others such as thiuramis sulfide, quinonedioxime thiol,
Examples include dithioic acids, but sulfur is usually used.
加硫促進剤としては、チアゾール系化合物の加硫促進剤
として、2−メルカプトベンゾチアゾールやその銅塩、
亜鉛塩、2.2−ジベンゾチアゾールジスルフィド等が
挙げられ、スルフェンアミド系化合物の加硫促進剤とし
て、N−シクロへキシル−2−ベンゾチアジルスルフェ
ンアミド、N−オキシジエチレン−2−ベンゾチアジル
スルフェンアミド、N、N’ −ジイソプロピル−2−
ベンゾチアジルスルフェンアミド等が挙げられ、チアゾ
リン系化合物の架橋促進剤として、2−メルカプトチア
ゾリン等が挙げられる。その他にも、チウラム系化合物
、ジチオカルバネート系化合物、アルデヒド・アミン系
化合物、グアニジン系化合物、カルバモイルチアゾール
系化合物等の加硫促進剤を使用することができる。As a vulcanization accelerator for thiazole compounds, 2-mercaptobenzothiazole and its copper salt,
Examples of vulcanization accelerators for sulfenamide compounds include zinc salts, 2,2-dibenzothiazole disulfide, and N-cyclohexyl-2-benzothiazylsulfenamide, N-oxydiethylene-2-benzo Thiadylsulfenamide, N,N'-diisopropyl-2-
Examples include benzothiazylsulfenamide, and examples of crosslinking accelerators for thiazoline compounds include 2-mercaptothiazoline. In addition, vulcanization accelerators such as thiuram compounds, dithiocarbanate compounds, aldehyde/amine compounds, guanidine compounds, and carbamoylthiazole compounds can be used.
ゴムラテックス及びゴムシートに配合される加硫剤の量
はゴム当り0.1乃至3重量%の範囲にあるのがよく、
0.5乃至2重量%の範囲にあるのが特に好ましい。ま
た、加硫促進剤の量は、加硫剤量、加硫条件等により適
当量を添加する。The amount of the vulcanizing agent added to the rubber latex and rubber sheet is preferably in the range of 0.1 to 3% by weight per rubber.
A range of 0.5 to 2% by weight is particularly preferred. Further, the amount of the vulcanization accelerator is added in an appropriate amount depending on the amount of the vulcanizing agent, vulcanization conditions, etc.
ゴムラテックス及びゴムシートにはそれ自体公知の配合
剤を公知の処方に従って配合することができ、例えばカ
ーボンブラック等の充填剤、プロセスオイル等の軟化剤
、老化防止剤、分散剤、可塑剤等を配合することができ
る。Rubber latex and rubber sheets can be compounded with compounding agents known per se according to known formulations, such as fillers such as carbon black, softeners such as process oil, anti-aging agents, dispersants, plasticizers, etc. Can be blended.
マット材料へのゴムラテックスの塗布方法としテハ、ロ
ールコータ−やスプレー、へヶによる塗布等、通常の塗
布方法により行うことができるが、ラテックスのゴム成
分が均一に分散していることが必要である。また、ゴム
ラテックスは、固形分としてマット材料に25乃至10
00g/m2、特に30乃至600 g/ln2の割合
いで塗布されていることが好ましく、塗布した後、ゴム
ラテックスが未加硫乃至半加硫の状態であるようにプレ
コート層を形成しなければならない。Rubber latex can be applied to the mat material using conventional methods such as coating with a roll coater, spray, or spacing, but it is necessary that the rubber components of the latex are uniformly dispersed. be. In addition, rubber latex has a solid content of 25 to 10% in the mat material.
It is preferable that the rubber latex be coated at a rate of 00 g/m2, especially 30 to 600 g/ln2, and after coating, a precoat layer must be formed so that the rubber latex is in an unvulcanized or semi-vulcanized state. .
このためにゴムラテックスの乾燥は、一般に90乃至1
80℃の温度及び1乃至120分間の条件から加硫剤及
び加硫促進剤の含有量によりプレコート層が未加硫乃至
半加硫となるような条件下で行う。For this reason, rubber latex is generally dried at 90 to 1
It is carried out at a temperature of 80° C. for 1 to 120 minutes under conditions such that the precoat layer becomes unvulcanized or semi-vulcanized depending on the content of the vulcanizing agent and vulcanization accelerator.
ゴムシートの目付量は100乃至4000g/m’、特
に200乃至2000g/m2とするのがよい。The basis weight of the rubber sheet is preferably 100 to 4000 g/m', particularly 200 to 2000 g/m2.
(実施例)
実施例 1
カットパイル
上記の材料のマットを作製し、プレコート層の乾燥、加
硫条件として2水準を設けた。(Examples) Example 1 Cut pile A mat of the above material was prepared, and two levels of drying and vulcanization conditions were set for the precoat layer.
乾燥機で150℃、20分の乾燥を行いプレコート層が
未加硫乃至は半加硫の状態のものをマットA、150℃
、60分の乾燥を行いプレコート層が完全加硫の状態の
ものをマットBとする。Dry in a dryer at 150°C for 20 minutes, and the precoat layer is uncured or semi-vulcanized as Matte A at 150°C.
Matte B is obtained by drying for 60 minutes and the precoat layer is completely vulcanized.
これらのマットA、Bをそれぞれ70X85cmに切断
して次の要領で一体化マットを作製した。These mats A and B were each cut to 70 x 85 cm to produce an integrated mat in the following manner.
加硫剤(硫黄)1重量%及び加硫促進剤(2−メルカプ
トベンゾチアゾール)1重量%を配合した厚さ4mmの
未加硫NBRシート上に上記寸法で切断したマットをの
せ、150℃で15分間、5にg/cm2の圧力でプレ
スを行うことにより接着・加硫を行いナイロンパイルの
一株化マットA、Bを作製した。The mat cut to the above dimensions was placed on an unvulcanized NBR sheet with a thickness of 4 mm containing 1% by weight of a vulcanizing agent (sulfur) and 1% by weight of a vulcanization accelerator (2-mercaptobenzothiazole), and heated at 150°C. Adhesion and vulcanization were performed by pressing at a pressure of 5 g/cm2 for 15 minutes to produce nylon pile mats A and B.
これらのマットを、通行人数3000人/日の場所に3
日間敷設した後、通常の一体化マットの洗浄再生処理を
行う。この操作を20回繰返し行った後、パイル抜糸強
度、基布−ゴム間の接着強度を測定した結果を表1に示
す。Place these mats in 3 locations with 3,000 pedestrians per day.
After being laid for several days, the conventional integrated mat cleaning and regeneration process is carried out. After repeating this operation 20 times, the pile thread removal strength and the adhesive strength between the base fabric and the rubber were measured, and the results are shown in Table 1.
また、使用前及びレンタル洗浄再生20回後のマットの
波打ちの程度を波打ちの高さ(mm)及び個数で表1に
示した。In addition, Table 1 shows the degree of waviness of the mat before use and after 20 rental cleaning and regenerations in terms of the height (mm) and number of waviness.
尚、抜糸強度及び、接着強度(基布−ゴム間)の試験は
、JIS L 1021 バイル糸引抜き強さ、裏張
り材の剥離強さの項に従って行った。The tests for thread removal strength and adhesion strength (between base fabric and rubber) were carried out in accordance with JIS L 1021 Vile thread pullout strength and peel strength of lining material.
実施例 2
上記の材料のマットでプレコート層を90℃で20分間
乾燥し、未加硫の状態であるマットCを作製し、プレコ
ート層を設けない以外はマットCと画質のマットDも併
せて作製して、それぞれ、実施例1と同様に一株化マッ
トC,Dを作製した。これらのマットについて実施例1
と同様の試験を行い、パイル抜糸強度を測定した。測定
結果を表1に示す。Example 2 A precoat layer of a mat made of the above material was dried at 90°C for 20 minutes to produce matte C in an unvulcanized state, and matte C and image quality matte D were also combined, except that no precoat layer was provided. Then, single-stock mats C and D were produced in the same manner as in Example 1, respectively. Example 1 for these mats
A similar test was conducted to measure the pile suture removal strength. The measurement results are shown in Table 1.
実施例 3
実施例2と同様、上記材料のマットでプレコート層を1
50℃、20分間乾燥し、未加硫乃至半加硫の状態であ
るマットEを作製し、プレコート層を設けない以外はマ
ットEと同質のマットFも併せて作製し、それぞれ実施
例1と同様に一株化マットE、Fを作製した。これらの
マットについて実施例1と同様の試験と行い、パイル抜
糸強度を測定した。測定結果を表1に示す。Example 3 As in Example 2, one precoat layer was made of the mat of the above material.
Matte E was dried at 50°C for 20 minutes to produce matte E in an unvulcanized or semi-vulcanized state, and matte F, which was the same as matte E except that no precoat layer was provided, was also produced. Single-stock mats E and F were produced in the same manner. These mats were subjected to the same tests as in Example 1, and the pile removal strength was measured. The measurement results are shown in Table 1.
表 1
(発明の効果)
本発明によれば、上記表1からも明らかな通り、過酷な
洗浄再生処理に賦しても、抜糸強度、接着強度が低下し
にくいため、パイル糸の脱落やマットの波打ちが防止さ
れるのである。Table 1 (Effects of the Invention) According to the present invention, as is clear from Table 1 above, even when subjected to severe cleaning and regeneration treatment, the thread removal strength and adhesive strength are unlikely to decrease, resulting in pile threads falling off and matting. This prevents waving.
第1図は本発明の除塵用一体止マットの製造工程を説明
する側面図である。
1・・・・・・基布、2・・・・・・パイル糸、3・・
・・・・プレコート層、4・・・・・・ゴムシート。FIG. 1 is a side view illustrating the manufacturing process of the integral mat for dust removal of the present invention. 1...Base fabric, 2...Pile thread, 3...
...Precoat layer, 4...Rubber sheet.
Claims (5)
るマット材料のステッチ面にゴム固形分当り0.1乃至
3重量%の加硫剤及び加硫に必要な適量の加硫促進剤を
含有するゴムラテックスを塗布して、該ステッチ面に未
加硫乃至半加硫のゴムプレコート層を形成させ、該プレ
コートマット材料と、プレコート層と同種のゴム、0.
1乃至3重量%の加硫剤及び適量の加硫促進剤を含有す
る未加硫ゴムシートとを、該プレコート層とゴムシート
とが対面するように重ね合せて、加熱下にプレスし、該
プレコート層とゴムシートとの接着と、プレコート層及
びゴムシートの加硫とを行うことを特徴とする除塵用一
体化マットの製法。(1) A vulcanizing agent of 0.1 to 3% by weight per rubber solid content and an appropriate amount of vulcanization necessary for vulcanization are applied to the stitched surface of a mat material consisting of a base material and a pile tufted to the base material. A rubber latex containing an accelerator is applied to form an unvulcanized or semi-vulcanized rubber precoat layer on the stitched surface, and the precoat mat material, the same type of rubber as the precoat layer, and 0.00% rubber latex containing an accelerator are applied.
An unvulcanized rubber sheet containing 1 to 3% by weight of a vulcanizing agent and an appropriate amount of a vulcanization accelerator is stacked so that the precoat layer and the rubber sheet face each other, and pressed under heat. A method for producing an integrated mat for dust removal, characterized by adhering a precoat layer and a rubber sheet, and vulcanizing the precoat layer and rubber sheet.
/m^2の量で形成されている特許請求の範囲第1項記
載の製法。(2) Precoat layer has a solid content of 25 to 1000g
2. The manufacturing method according to claim 1, wherein the amount of carbon dioxide is formed in an amount of /m^2.
ブタジエンゴムである特許請求の範囲第1項記載の製法
。(3) The rubber of the precoat layer and rubber sheet is nitrile.
The manufacturing method according to claim 1, which is butadiene rubber.
含有しないゴム組成物から成り、未加硫ゴムシートが加
硫剤及び加硫促進剤を含有するゴム組成物から成る特許
請求の範囲第1項記載の製法。(4) A patent claim in which the precoat layer consists of a rubber composition containing a vulcanizing agent but not a vulcanization accelerator, and the unvulcanized rubber sheet consists of a rubber composition containing a vulcanizing agent and a vulcanization accelerator. The manufacturing method according to item 1.
ポリエステル繊維を含むパイル糸から成る特許請求の範
囲第1項記載の製法。(5) The manufacturing method according to claim 1, wherein the tufted pile is a pile yarn containing polyvinyl alcohol fiber or polyester fiber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62296107A JP2548752B2 (en) | 1987-11-26 | 1987-11-26 | Manufacturing method of integrated mat for dust removal |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62296107A JP2548752B2 (en) | 1987-11-26 | 1987-11-26 | Manufacturing method of integrated mat for dust removal |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01139253A true JPH01139253A (en) | 1989-05-31 |
JP2548752B2 JP2548752B2 (en) | 1996-10-30 |
Family
ID=17829226
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62296107A Expired - Lifetime JP2548752B2 (en) | 1987-11-26 | 1987-11-26 | Manufacturing method of integrated mat for dust removal |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2548752B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0662974U (en) * | 1993-02-22 | 1994-09-06 | 株式会社ダスキン | Tiled shoe cloth |
JP2009291962A (en) * | 2008-06-02 | 2009-12-17 | Ube Ind Ltd | Multilayered structure |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54127927A (en) * | 1978-03-29 | 1979-10-04 | Toyoda Gosei Co Ltd | Primer composition |
JPS57199653A (en) * | 1981-06-03 | 1982-12-07 | Hitachi Cable | Waterproof execution method |
JPS6268829A (en) * | 1985-09-19 | 1987-03-28 | Toray Silicone Co Ltd | Primer composition |
JPS62217934A (en) * | 1986-03-20 | 1987-09-25 | 株式会社ダスキン | Production of backing mat |
-
1987
- 1987-11-26 JP JP62296107A patent/JP2548752B2/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54127927A (en) * | 1978-03-29 | 1979-10-04 | Toyoda Gosei Co Ltd | Primer composition |
JPS57199653A (en) * | 1981-06-03 | 1982-12-07 | Hitachi Cable | Waterproof execution method |
JPS6268829A (en) * | 1985-09-19 | 1987-03-28 | Toray Silicone Co Ltd | Primer composition |
JPS62217934A (en) * | 1986-03-20 | 1987-09-25 | 株式会社ダスキン | Production of backing mat |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0662974U (en) * | 1993-02-22 | 1994-09-06 | 株式会社ダスキン | Tiled shoe cloth |
JP2009291962A (en) * | 2008-06-02 | 2009-12-17 | Ube Ind Ltd | Multilayered structure |
Also Published As
Publication number | Publication date |
---|---|
JP2548752B2 (en) | 1996-10-30 |
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