JPH01139254A - Production of dust-arresting integrated mat - Google Patents
Production of dust-arresting integrated matInfo
- Publication number
- JPH01139254A JPH01139254A JP29610887A JP29610887A JPH01139254A JP H01139254 A JPH01139254 A JP H01139254A JP 29610887 A JP29610887 A JP 29610887A JP 29610887 A JP29610887 A JP 29610887A JP H01139254 A JPH01139254 A JP H01139254A
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- precoat layer
- rubber sheet
- mat
- crosslinked
- 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 12
- 229920001971 elastomer Polymers 0.000 claims abstract description 62
- 239000005060 rubber Substances 0.000 claims abstract description 59
- 239000000463 material Substances 0.000 claims abstract description 25
- 238000004073 vulcanization Methods 0.000 claims abstract description 18
- 229920000126 latex Polymers 0.000 claims abstract description 17
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 16
- 239000003431 cross linking reagent Substances 0.000 claims abstract description 9
- 239000000835 fiber Substances 0.000 claims description 10
- 239000000428 dust Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229920000459 Nitrile rubber Polymers 0.000 claims description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 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
- 239000004636 vulcanized rubber Substances 0.000 claims 1
- 239000004744 fabric Substances 0.000 abstract description 10
- 230000008929 regeneration Effects 0.000 abstract description 5
- 238000011069 regeneration method Methods 0.000 abstract description 5
- 238000004140 cleaning 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
- 238000011282 treatment Methods 0.000 description 4
- 239000000806 elastomer Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 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
- 238000004132 cross linking Methods 0.000 description 2
- -1 etc. Chemical class 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 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
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- 229940090898 Desensitizer Drugs 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000002174 Styrene-butadiene 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
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 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
- 230000021523 carboxylation Effects 0.000 description 1
- 238000006473 carboxylation reaction Methods 0.000 description 1
- 238000013329 compounding Methods 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
- 239000002270 dispersing agent Substances 0.000 description 1
- PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 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
- 238000007731 hot pressing Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 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
- 238000005259 measurement Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000000203 mixture 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
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920002857 polybutadiene 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
- 239000007921 spray Substances 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
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Laminated Bodies (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は除塵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化マットの製法に関
する。Detailed Description of the Invention (Field of Industrial Application) The present invention relates to a method for manufacturing an integrated mat for dust removal, and more specifically, the present invention relates to a method for manufacturing an integrated mat for dust removal. 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. Concerning the manufacturing method of matte.
(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應用一
体化マットとして、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 de-escorting mat used by laying at entrances and exits such as entrances, it is well known that rubber and vinyl chloride sheets are integrated into the backstitched surface of a tufted mat. There is.
この一体化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 integrated mat can be produced by attaching 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 mat fibers 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)
これらの一体化マットは、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、この傾向か特に大であった。(Problems to be Solved by the Invention) Since these integrated mats are installed at entrances and exits for people, the pile surface is repeatedly subjected to friction from the soles of shoes. Furthermore, since the mats are used in a rental system where the mats are washed and regenerated after being used for a certain period of time and then rented out again, the mats may become wavy due to the expansion and contraction of the mat material due to repeated friction and washing treatments as described above. The disadvantage is that this occurs. Another problem is that the pile threads fall off the mat, causing the mat to become thinner. In particular, polyvinyl alcohol fibers and polyester fibers, which have excellent texture and durability, have poor adhesion to rubber. This trend was particularly large.
従って、本発明の目的は、パイル糸をゴムバッキングに
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化マットの
製法を提供するにある。Therefore, an object of the present invention is to firmly adhesively fix the pile yarn to the rubber backing, thereby preventing the pile yarn from falling off or waving even after repeated washing and regeneration, and significantly improving dimensional stability. An object of the present invention is to provide a method for manufacturing an improved integrated mat for dust removal.
(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六イル
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10重量%架橋剤を含有するゴムラテックスを
塗布して、該ステッチ面に架橋乃至半架橋のゴムプレコ
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、0,3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、プレコート層の架橋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−体化マットの製法が提
供される。(Means for Solving the Problems) According to the present invention, the stitched surface of a mat material consisting of a base material and a rubber tufted on the base material has a rubber solid content of 0.
.. A rubber latex containing 1 to 10% by weight of a crosslinking agent is applied to form a crosslinked or semi-crosslinked rubber precoat layer on the stitched surface, and the precoat mat material and the same type of rubber as the precoat layer are coated. An unvulcanized rubber sheet containing 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 layer. Provided is a method for producing a dust-removing mat, which is characterized by adhering a rubber sheet to a rubber sheet, crosslinking a precoat layer, and vulcanizing the rubber sheet.
(作用)
本発明によれば、架橋剤を含有するゴムラテックスを架
橋乃至半架橋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−休止が可能となる。(Function) According to the present invention, rubber latex containing a crosslinking agent is provided as a precoat layer on the stitched surface of the mat material in a crosslinked or semi-crosslinked state. This makes it possible to infiltrate the mat material with the rubber component in advance, and also enables strong adhesion to the rubber sheet applied later.
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。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強固で寸法安定性及
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ていることと、ゴム自体に架橋
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 strong, dimensionally stable, and durable adhesive structure at the interface between the mat material and the rubber sheet, it is necessary to infiltrate the rubber component into the mat material and introduce a crosslinked structure into the rubber itself. Both are necessary.
本発明によればプレコート層を架橋乃至半架橋の状態で
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。この加熱プレス時における
プレコート層の加硫はゴムシート中に含有されている加
硫剤及び加硫促進剤がプレコート層中に拡散移行するこ
とにより架橋されたプレコート層及びゴムシート界面で
再度加硫し、未加硫ゴムを加硫接着する場合と同様に効
果的に行われるものである。According to the present invention, the precoat layer is provided in a crosslinked or semi-crosslinked state, and an unvulcanized rubber sheet is pressed onto the precoat layer under heat to simultaneously integrate and vulcanize the two. This prevents pile threads from falling off, peeling of the original fabric, and ripples. The vulcanization of the precoat layer during this hot pressing is performed by the vulcanizing agent and vulcanization accelerator contained in the rubber sheet diffusing and transferring into the precoat layer, resulting in re-vulcanization at the crosslinked interface between the precoat layer and the rubber sheet. However, it is carried out effectively in the same way as when unvulcanized rubber is vulcanized and bonded.
(発明の好適な態様)
本発明の除塵用一体化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 integrated 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)に架橋剤を
含有するゴムラテックスを塗布して架橋乃至半架橋のブ
し・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, rubber latex containing a crosslinking agent is applied to the back side (stitched side) of the base fabric 1 to form a crosslinked or semi-crosslinked brush/coat 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、紡績糸或い
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 yarns, or blended yarns thereof, conventional natural fibers can also be used.
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、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
。またゴムラテックスとしても同様にニトリル−ブタジ
エンゴムが特に好適に使用されるが、他のカルボキシル
化変性ラテックス、例えばSBR,CR,BR,イソプ
レン、またビニルとリジンラテックス等を用いる事もで
きる。As the elastomer used for the rubber sheet, nitrile-butadiene rubber is particularly preferably used, but other vulcanizable rubbers such as styrene-butadiene copolymer rubber (
5BR), chloroprene rubber, polybutadiene rubber, chlorosulfonated polyethylene, etc. can also be used. Similarly, nitrile-butadiene rubber is particularly preferably used as the rubber latex, but other carboxylated modified latexes such as SBR, CR, BR, isoprene, vinyl and lysine latex, etc. can also be used.
また、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
フイド、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 to be mixed into the rubber sheet, inorganic vulcanizing agents include metal salts such as sulfur, zinc chloride, ferrous chloride, tin chloride, sulfur chloride, etc., and organic peroxides. Examples of the vulcanizing agent include dicumyl peroxide, acetylene peroxide, benzoyl peroxide, and ethyl methyl ketone peroxide.Other examples include thiuramis sulfide, quinone dioximthiol, and dithioic acid. It is common to use
カルボキシル化変性ゴムラテックスに配合される架橋剤
として
グリコール HOCH2−CH20Hアミン
RI NH2
多価金属酸化物 MeO
多価金属塩および水酸化物 MeX
を挙げることができる。Glycol HOCH2-CH20H amine as a crosslinking agent blended into carboxylated modified rubber latex
Mention may be made of RI NH2 polyvalent metal oxides MeO polyvalent metal salts and hydroxides MeX.
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
、ジチオカルバメート系化合物、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。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, thiuram compounds, dithiocarbamate compounds, aldehyde/amine compounds, guanidine compounds, carbamoylthiazole compounds, etc.
加硫促進剤を使用することができる。Vulcanization accelerators can be used.
ゴムラテックスに配合される架橋剤の量は0.1乃至1
0重量%の範囲にあるのが好ましく特に1〜5の範囲に
あるのが好ましい。The amount of crosslinking agent added to the rubber latex is 0.1 to 1
It is preferably in the range of 0% by weight, particularly preferably in the range of 1 to 5%.
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、ゴムシートに配
合される加硫促進剤の量は、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 blended into the rubber sheet is preferably in the range of 0.1 to 3% by weight, and 0.5 to 2% by weight per rubber.
It is particularly preferable that it be within the range of . The amount of vulcanization accelerator to be added to the rubber sheet is determined depending on the amount of 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、可望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, desensitizers, 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ては、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かできるが、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、マット材料に25乃至1000g/m2
、特に30乃至600 g/rn2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
架橋乃至半架橋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 roll coater, spray, and spacing, but it is necessary that the rubber components of the latex are uniformly dispersed. be. In addition, rubber latex is applied to the mat material at a rate of 25 to 1000 g/m2.
It is particularly preferable that the rubber latex be coated at a rate of 30 to 600 g/rn2, and after coating, the precoat layer must be formed so that the rubber latex is in a crosslinked or semi-crosslinked 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分間の条件から架橋剤の
含有量によりプレコート層が架橋乃至半架橋となるよう
な条件下で行う。For this reason, rubber latex is generally dried at 90 to 1
The coating is carried out at a temperature of 80° C. and for 1 to 120 minutes under conditions such that the precoat layer becomes crosslinked or semi-crosslinked depending on the content of the crosslinking agent.
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
カルボキシル化
上記の材料のマットを作成し、プレコート層を150℃
で20分間乾燥、キユアリングし架橋状態であるマット
を作製し、プレコート層を設けない以外はマットAと同
質のマットBもあわせて作製した。(Example) Example 1 Cut pile carboxylation A mat of the above material was created, and a precoat layer was heated at 150°C.
A mat in a crosslinked state was prepared by drying and curing for 20 minutes, and a mat B, which was the same as mat A except that no precoat layer was provided, was also prepared.
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(01+11)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 (01+11) 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150℃で10分
間乾燥し、架橋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同様のマットDを作製して、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 150°C for 10 minutes to produce a crosslinked mat C, and a similar mat D except that no precoat layer was provided, and each was carried out. Single-stock mats C and D were produced in the same manner as in Example 1. These mats were subjected to the same test 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
ないため、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, the removal strength and adhesive strength do not decrease even when subjected to severe washing and regeneration treatment, so that pile yarns do not fall off or mats do not form. This prevents ripples.
第1図は本発明の除塵用一体化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。
特許出願人 株式会社 ダ ス キ ンt′・ ・
、
代理人 弁理士 鈴木郁男(1、・・
・・J′!ンFIG. 1 is a side view illustrating the manufacturing process of the integrated dust removal mat of the present invention. 1...Base fabric, 2...Pile thread, 3...
...Precoat layer, 4...Rubber sheet. Patent applicant Daskin Co., Ltd.
, Agent Patent Attorney Ikuo Suzuki (1,...J'!n
Claims (4)
るマット材料のステッチ面にゴム固形分当り0.1乃至
10重量%架橋剤を含有するカルボキシル化変性ゴムラ
テックスを塗布して、該ステッチ面に架橋乃至半架橋の
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、プレコート層の架橋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 carboxylated modified rubber latex containing 0.1 to 10% by weight of a crosslinking agent per solid rubber content is applied to the stitched surface of a mat material consisting of a base material and a pile tufted to the base material. , a crosslinked or semi-crosslinked rubber precoat layer is formed on the stitched surface, and a precoat material containing the precoat mat material, the same type of rubber as the precoat layer, and 0.1 to 3% by weight of a vulcanizing agent and a vulcanization accelerator. A vulcanized rubber sheet is stacked so that the precoat layer and the rubber sheet face each other and pressed under heat to bond the precoat layer and the rubber sheet, crosslink the precoat layer, and vulcanize the rubber sheet. A method for manufacturing an integrated mat for dust removal, characterized by performing the following steps.
/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.
ある特許請求の範囲第1項記載の製法。(3) The manufacturing method according to claim 1, wherein the rubber of the rubber sheet is nitrile-butadiene rubber.
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。(4) 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 |
---|---|---|---|
JP62296108A JP2615092B2 (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 |
---|---|---|---|
JP62296108A JP2615092B2 (en) | 1987-11-26 | 1987-11-26 | Manufacturing method of integrated mat for dust removal |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01139254A true JPH01139254A (en) | 1989-05-31 |
JP2615092B2 JP2615092B2 (en) | 1997-05-28 |
Family
ID=17829239
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62296108A Expired - Lifetime JP2615092B2 (en) | 1987-11-26 | 1987-11-26 | Manufacturing method of integrated mat for dust removal |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2615092B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006101911A (en) * | 2004-09-30 | 2006-04-20 | Ono:Kk | Dust control mat |
CN110438832A (en) * | 2019-05-23 | 2019-11-12 | 山东海工科技有限公司 | Wear-resisting type hangs clothing rope and preparation method thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62137028A (en) * | 1985-12-09 | 1987-06-19 | 株式会社 ダスキン | Integrated mat |
JPS62137029A (en) * | 1985-12-09 | 1987-06-19 | 株式会社ダスキン | Production of integrated mat |
-
1987
- 1987-11-26 JP JP62296108A patent/JP2615092B2/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62137028A (en) * | 1985-12-09 | 1987-06-19 | 株式会社 ダスキン | Integrated mat |
JPS62137029A (en) * | 1985-12-09 | 1987-06-19 | 株式会社ダスキン | Production of integrated mat |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006101911A (en) * | 2004-09-30 | 2006-04-20 | Ono:Kk | Dust control mat |
JP4573028B2 (en) * | 2004-09-30 | 2010-11-04 | 株式会社オーノ | Dust control mat |
CN110438832A (en) * | 2019-05-23 | 2019-11-12 | 山东海工科技有限公司 | Wear-resisting type hangs clothing rope and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2615092B2 (en) | 1997-05-28 |
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