JPH04245976A - Textile treated with vinyl chloride resin - Google Patents
Textile treated with vinyl chloride resinInfo
- Publication number
- JPH04245976A JPH04245976A JP3223791A JP3223791A JPH04245976A JP H04245976 A JPH04245976 A JP H04245976A JP 3223791 A JP3223791 A JP 3223791A JP 3223791 A JP3223791 A JP 3223791A JP H04245976 A JPH04245976 A JP H04245976A
- Authority
- JP
- Japan
- Prior art keywords
- vinyl chloride
- chloride resin
- fabric
- coated
- treated
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000011347 resin Substances 0.000 title claims abstract description 45
- 229920005989 resin Polymers 0.000 title claims abstract description 45
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 title claims abstract description 39
- 239000004753 textile Substances 0.000 title abstract 2
- 239000004744 fabric Substances 0.000 claims abstract description 30
- -1 alkyl vinyl ether Chemical compound 0.000 claims abstract description 9
- 229920001577 copolymer Polymers 0.000 claims abstract description 8
- 239000002904 solvent Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 abstract description 11
- 239000011248 coating agent Substances 0.000 abstract description 10
- 239000004014 plasticizer Substances 0.000 abstract description 6
- 229920000728 polyester Polymers 0.000 abstract description 5
- 239000000835 fiber Substances 0.000 abstract description 3
- 239000002759 woven fabric Substances 0.000 abstract description 3
- 239000011342 resin composition Substances 0.000 abstract description 2
- 238000000034 method Methods 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 8
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 230000003373 anti-fouling effect Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 4
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- SKYXLDSRLNRAPS-UHFFFAOYSA-N 1,2,4-trifluoro-5-methoxybenzene Chemical compound COC1=CC(F)=C(F)C=C1F SKYXLDSRLNRAPS-UHFFFAOYSA-N 0.000 description 2
- HMBNQNDUEFFFNZ-UHFFFAOYSA-N 4-ethenoxybutan-1-ol Chemical compound OCCCCOC=C HMBNQNDUEFFFNZ-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 229920002978 Vinylon Polymers 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229920003235 aromatic polyamide Polymers 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 125000006165 cyclic alkyl group Chemical group 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- JQCXWCOOWVGKMT-UHFFFAOYSA-N phthalic acid diheptyl ester Natural products CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC JQCXWCOOWVGKMT-UHFFFAOYSA-N 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は,トラツクシート,野積
シート,大型テント等に使用される塩化ビニル樹脂加工
布に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a vinyl chloride resin-treated fabric used for truck seats, outdoor seats, large tents, etc.
【0002】0002
【従来の技術】従来から,塩化ビニル系樹脂を被覆加工
したテント,トラツクシート等についてはよく知られて
いる。これらは,ビニロン,ポリアミド,ポリエステル
,アラミド等の紡績糸または長繊維糸を用いて製編織し
た布帛に,塩化ビニル系樹脂を用いてデイツピング,コ
ーテイング,トツピング,ラミネーテイング等の種々の
方法により加工を施して製造されている。BACKGROUND OF THE INVENTION Tents, track sheets, etc. coated with vinyl chloride resin have been well known. These fabrics are made by knitting and weaving fabrics using spun yarns or long fiber yarns such as vinylon, polyamide, polyester, aramid, etc., and are processed by various methods such as dipping, coating, topping, and laminating using vinyl chloride resin. It is manufactured by applying
【0003】塩化ビニル系樹脂が広く用いられている理
由としては,加工性が優れており,種々の加工方法が採
用でき,また,可塑剤の調整により任意に樹脂の柔軟性
を調整できること,さらに,軟質塩化ビニル系樹脂が高
周波ウエルダー溶着加工による縫製を行い得ることが挙
げられる。[0003] The reason why vinyl chloride resin is widely used is that it has excellent processability, various processing methods can be adopted, and the flexibility of the resin can be adjusted arbitrarily by adjusting the plasticizer. , Soft vinyl chloride resin can be sewn using high-frequency welder welding processing.
【0004】上記のごとく,塩化ビニル系樹脂加工布は
,多くの長所を有しているが,長期間屋外で曝露されて
使用されるため,汚れやすい。すなわち,塩化ビニル系
樹脂加工布は,塩化ビニル系樹脂中の可塑剤の表面への
移行が使用中に徐々に進行し,粘着性を帯びて大気中の
汚れが付着しやすく,外観が著しく悪化する。このよう
な問題を解決する方法として種々提案されているが,そ
の代表的なものとしては,加工布の表面をポリアクリル
酸エステル等のアクリル酸系樹脂あるいはウレタン系樹
脂でコーイングする方法がある。しかしながら,該アク
リル酸系樹脂およびウレタン系樹脂をコーテイングする
方法では,塩化ビニル系樹脂中の可塑剤がアクリル酸系
樹脂およびウレタン系樹脂の層を通り表面移行するため
効果の持続性が乏しい。また,テトラフルオロエチレン
フイルム等弗素系フイルム等をラミネートする方法は,
防汚性能は優れているがコスト面で不利であり,弗素系
エラストマーで被覆する方法(例えば特開平1−321
980号)では,耐久防汚性が充分に得られず,その他
の方法も含めて防汚性能,耐久性,加工性およびコスト
等を全て満足する方法は未だ見出されていない。As mentioned above, vinyl chloride resin-treated fabrics have many advantages, but they tend to get dirty because they are exposed outdoors for long periods of time. In other words, with vinyl chloride resin-treated cloth, the plasticizer in the vinyl chloride resin gradually migrates to the surface during use, becoming sticky and easily attracting dirt from the atmosphere, resulting in a noticeable deterioration in appearance. do. Various methods have been proposed to solve these problems, and a typical method is to coat the surface of the processed cloth with an acrylic resin such as polyacrylic acid ester or a urethane resin. However, in this method of coating with acrylic acid resin and urethane resin, the plasticizer in the vinyl chloride resin migrates to the surface through the layer of acrylic acid resin and urethane resin, resulting in poor sustainability of the effect. In addition, the method of laminating fluorine-based films such as tetrafluoroethylene films is as follows.
Although it has excellent antifouling performance, it is disadvantageous in terms of cost.
No. 980), it was not possible to obtain sufficient durable antifouling properties, and no method, including other methods, that satisfies all of the antifouling performance, durability, workability, cost, etc. has yet been found.
【0005】[0005]
【発明が解決しようとする課題】本発明は,このような
現状に鑑みて行われたもので,耐久性に優れた防汚性を
有する塩化ビニル樹脂加工布を得ることを目的とするも
のである。[Problems to be Solved by the Invention] The present invention was made in view of the current situation, and its purpose is to obtain a vinyl chloride resin-treated cloth that has excellent durability and antifouling properties. be.
【0006】[0006]
【課題を解決するための手段】本発明は,上記目的を達
成するもので,次の構成よりなるものである。すなわち
,本発明は,塩化ビニル系樹脂を主成分とする加工剤に
て被覆されている加工布であって,フルオロオレフイン
とアルキルビニルエーテルの共重合体を主体とした溶剤
系弗素樹脂による被覆、架橋化処理が施されてなること
を特徴とする塩化ビニル樹脂加工布を要旨とするもので
ある。以下,本発明を詳細に説明する。[Means for Solving the Problems] The present invention achieves the above object and has the following configuration. That is, the present invention relates to a processed fabric coated with a processing agent containing a vinyl chloride resin as a main component, which is coated with a solvent-based fluororesin mainly composed of a copolymer of fluoroolefin and alkyl vinyl ether, and cross-linked. The gist of this invention is a vinyl chloride resin-treated cloth characterized by being subjected to a chemical treatment. The present invention will be explained in detail below.
【0007】ここでいう塩化ビニル系樹脂とは,塩化ビ
ニル重合体,塩化ビニル−酢酸ビニル共重合体,塩化ビ
ニル−塩化ビニリデン共重合体あるいは前記重合体また
は共重合体の混合物に安定剤,可塑剤,防炎剤,その他
の添加剤を配合した樹脂を意味する。[0007] The vinyl chloride resin mentioned here refers to a vinyl chloride polymer, a vinyl chloride-vinyl acetate copolymer, a vinyl chloride-vinylidene chloride copolymer, or a mixture of the above polymers or copolymers with a stabilizer and a plasticizer. Refers to resins containing additives, flame retardants, and other additives.
【0008】本発明で用いる布帛としては,綿,レーヨ
ンおよびポリアミド,ポリエステル,ポリアラミド,ビ
ニロン等の合成繊維の紡績糸あるいは長繊維糸を用いて
所望の組織で製編織した編織物である。The fabric used in the present invention is a knitted fabric made of cotton, rayon, and synthetic fibers such as polyamide, polyester, polyaramid, vinylon, etc. spun or long fiber yarn in a desired structure.
【0009】また,本発明のフルオロオレフインとアル
キルビニルエーテルの重合物としては,フルオロオレフ
インおよびアルキルビニルエーテルに基づく単位をそれ
ぞれ40〜60モル%および60〜40モル%含有し,
テトラヒドロフラン中で30℃において測定される固有
粘度が0.03〜1.5dl/gであるものが挙げられ
る。
好ましいフルオロオレフイン成分としては,テトラフル
オロエチレンおよびクロロトリフルオロエチレンが,ま
た,好ましいアルキルビニルエーテル成分としては,一
般式CH2=CHORにおいてRが炭素数2〜10であ
る直鎖状,分枝状もしくは脂環状のアルキル基並びに炭
素数2〜8である直鎖状,分枝状もしくは脂環状のヒド
ロキシ基含有アルキル基であるものが挙げられる。具体
的な例としては,フルオロオレフイン成分としてはクロ
ロトリフルオロエチレン(CTFE)を用い,アルキル
ビニルエーテル成分としてはシクロヘキシルビニルエー
テル(CHVE),エチルビニルエーテル(EVE)お
よびヒドロキシブチルビニルエーテル(HBVE)を用
い,それぞれのモル比が50.0/14.8/25.8
/9.8で共重合させたものが挙げられる。この重合体
は,加工性が良好で塩化ビニル系樹脂にノンプライマー
でコートでき,その密着性も良好である。Further, the polymer of fluoroolefin and alkyl vinyl ether of the present invention contains 40 to 60 mol% and 60 to 40 mol% of units based on fluoroolefin and alkyl vinyl ether, respectively,
Examples include those having an intrinsic viscosity of 0.03 to 1.5 dl/g as measured in tetrahydrofuran at 30°C. Preferred fluoroolefin components include tetrafluoroethylene and chlorotrifluoroethylene, and preferred alkyl vinyl ether components include linear, branched, or aliphatic compounds in which R has 2 to 10 carbon atoms in the general formula CH2=CHOR. Examples include cyclic alkyl groups and linear, branched, or alicyclic hydroxy group-containing alkyl groups having 2 to 8 carbon atoms. As a specific example, chlorotrifluoroethylene (CTFE) is used as the fluoroolefin component, and cyclohexyl vinyl ether (CHVE), ethyl vinyl ether (EVE), and hydroxybutyl vinyl ether (HBVE) are used as the alkyl vinyl ether components. Molar ratio is 50.0/14.8/25.8
Examples include those copolymerized with /9.8. This polymer has good processability, can be coated on vinyl chloride resin without a primer, and has good adhesion.
【0010】本発明では,フルオロオレフインとアルキ
ルビニルエーテルの重合物の不飽和基を三次元的に架橋
させ,皮膜強度の向上による耐久性の向上をはかる為に
,該重合物にイソシアネートを併用する。好ましいイソ
シアネートとしては,ジフエニルメタンジイソシアネー
ト,2,4トルエンジイソシアネート等が挙げられる。
イソシアネートの使用量としては,固形分換算で混合樹
脂の10〜30wt%であり,10%以下では十分に架
橋されないので,皮膜強度が弱く,また30%以上では
イソシアネートのモノマーが残る可能性がある。また,
ベースとなる塩化ビニル系樹脂加工布の耐光性を向上さ
せる為に,紫外線吸収剤等を入れることも可能である。In the present invention, an isocyanate is used in combination with the polymer of fluoroolefin and alkyl vinyl ether in order to three-dimensionally crosslink the unsaturated groups of the polymer and improve durability by increasing film strength. Preferred isocyanates include diphenylmethane diisocyanate, 2,4 toluene diisocyanate, and the like. The amount of isocyanate used is 10 to 30 wt% of the mixed resin in terms of solid content; if it is less than 10%, sufficient crosslinking will not occur, resulting in weak film strength, and if it is more than 30%, isocyanate monomer may remain. . Also,
In order to improve the light resistance of the base vinyl chloride resin-treated fabric, it is also possible to add an ultraviolet absorber or the like.
【0011】混合溶媒としては,揮発性の高いトルエン
に代表される芳香族炭化水素,メチルエチルケトンに代
表されるケトン類を各々単独で,または混合して用いる
。塩化ビニル系樹脂加工布を調整した混合樹脂で被覆す
る方法としては,パツデイング,あるいはグラビアコー
テイングやナイフコーテイング等のコーテイング等の方
法が採用できる。付着量については,その性能を十分満
足させるために,固形分で1〜20g/m2 塗布する
ことが必要である。付着量が1g/m2 より少ないと
その効果は認められず,20g/m2 より多いとクラ
ツクが生じ,均一に塗布することが不可能となる。As the mixed solvent, highly volatile aromatic hydrocarbons typified by toluene and ketones typified by methyl ethyl ketone are used either singly or in combination. As a method for coating the vinyl chloride resin-treated cloth with a prepared mixed resin, coating methods such as padding, gravure coating, knife coating, etc. can be employed. Regarding the amount of coating, in order to fully satisfy the performance, it is necessary to apply the coating at a solid content of 1 to 20 g/m2. If the amount of adhesion is less than 1 g/m2, no effect will be observed, and if it is more than 20 g/m2, cracks will occur and it will be impossible to apply uniformly.
【0012】フルオロオレフインとアルキルビニルエー
テルの重合物の不飽和基の架橋反応は,塩化ビニル系樹
脂加工布への混合樹脂の被覆後に行うが,この架橋反応
は温度150℃以下で行う。150℃を超えると,塩化
ビニル系樹脂の軟化し始めるため,加工が困難であり,
十分な防汚性能が得られない。本発明は,以上の構成を
持つものである。[0012] The crosslinking reaction of the unsaturated groups of the polymer of fluoroolefin and alkyl vinyl ether is carried out after coating the vinyl chloride resin-treated fabric with the mixed resin, and this crosslinking reaction is carried out at a temperature of 150°C or lower. When the temperature exceeds 150℃, the vinyl chloride resin begins to soften, making processing difficult.
Sufficient antifouling performance cannot be obtained. The present invention has the above configuration.
【0013】[0013]
【作 用】本発明の塩化ビニル樹脂加工布は,塩化ビ
ニル系樹脂層をフルオロオレフインとアルキルビニルエ
ーテル共重合体を主体とした溶剤系弗素樹脂で被覆して
いるので,使用中汚れが付きにくく,かつ塩化ビニル樹
脂表面の耐水圧を向上させることができる。[Function] The vinyl chloride resin-treated cloth of the present invention has a vinyl chloride resin layer coated with a solvent-based fluororesin mainly composed of fluoroolefin and alkyl vinyl ether copolymer, so it is difficult to get dirty during use. Moreover, the water pressure resistance of the vinyl chloride resin surface can be improved.
【0014】[0014]
【実施例】実施例1
経糸,緯糸ともにポリエステルマルチフイラメント糸7
50デニール/70フイラメントを用い,織密度が経2
0本/インチ,緯21本/インチの平織組織の織物を製
織し,この生機を185℃,30秒の条件でヒートセツ
トし,これを基布として下記組成−1の塩化ビニル系樹
脂組成物によりトツピング加工(加工温度170℃,塗
布量50g/m2 )を両面に施し,180℃で焼付け
加工を行って塩化ビニル系樹脂加工布を作製した。[Example] Example 1 Both warp and weft are polyester multifilament yarn 7
Using 50 denier/70 filament, weave density is 2
A woven fabric with a plain weave structure of 0 threads/inch and a weft of 21 threads/inch was woven, this gray fabric was heat set at 185°C for 30 seconds, and this was used as a base fabric with a vinyl chloride resin composition having the following composition-1. Topping processing (processing temperature: 170°C, coating amount: 50 g/m2) was applied to both sides, and baking processing was performed at 180°C to produce a vinyl chloride resin-treated cloth.
【0015】〔組 成−1〕
・塩化ビニル樹脂コンパウンド
100重量部
・ジ−N−オクチルフタレート(可塑剤) 60重量
部 ・炭酸カルシウム(充填剤)
20重量部
・ステアリン酸鉛(安定剤)
3重量部 ・顔
料
10重量部[Composition-1] - Vinyl chloride resin compound
100 parts by weight
・Di-N-octyl phthalate (plasticizer) 60 parts by weight ・Calcium carbonate (filler)
20 parts by weight
・Lead stearate (stabilizer)
3 parts by weight ・Face
fee
10 parts by weight
【0016】次に,下記組
成−2の加工溶液により,上記の塩化ビニル系樹脂加工
布の片面にナイフコータを用いてコーテイング加工(固
形分10g/m2)を行った。
〔組 成−2〕
・フロロトツプFT−1030
100重量部
(フルオロオレフインとアルキルビニルエ
ーテル共重合体 有効成分
50%,旭硝子株式会社製) ・フ
ロロトツプ硬化剤
20重量部 (
イソシアネート,有効成分67.6%,旭硝子株式会社
製)乾燥(80℃,2分間)後,130℃で2分間の架
橋化の為の熱処理を行った。[0016]Next, one side of the vinyl chloride resin-treated cloth was coated with a processing solution having the following composition-2 using a knife coater (solid content: 10 g/m2). [Composition-2] ・Florotop FT-1030
100 parts by weight
(Fluoroolefin and alkyl vinyl ether copolymer, active ingredient 50%, manufactured by Asahi Glass Co., Ltd.) - Fluorotop hardener
20 parts by weight (
After drying (80° C., 2 minutes), heat treatment for crosslinking was performed at 130° C. for 2 minutes.
【0017】比較例1
実施例1における組成−2の加工溶液によるコーテイン
グ加工を行う前の塩化ビニル樹脂加工布を比較例1とし
た。Comparative Example 1 Comparative Example 1 was a vinyl chloride resin-treated cloth before being coated with the processing solution of Composition-2 in Example 1.
【0018】比較例2
実施例1における組成−2の加工溶液によるコーテイン
グ加工を行う前の塩化ビニル樹脂加工布に下記組成−3
の加工溶液により,片面にナイフコーターを用いてコー
テイング加工(固形分10g/m2)を行った。〔組
成−3〕
・セフラルソフト(有効成分20
%) 60重量部
(弗素系エラストマー,セントラル硝子製)
・メチルエチルケトン
40重量部乾燥
(100℃,2分間)後,150℃で2分間熱処理を行
った。Comparative Example 2 The following composition-3 was applied to the vinyl chloride resin-treated cloth before coating with the processing solution of composition-2 in Example 1.
Coating processing (solid content: 10 g/m2) was performed on one side using a knife coater using a processing solution of. 〔set
Sei-3] ・Cefural Soft (active ingredient 20
%) 60 parts by weight
(Fluorine-based elastomer, made by Central Glass)
・Methyl ethyl ketone
After drying 40 parts by weight (100°C, 2 minutes), heat treatment was performed at 150°C for 2 minutes.
【0019】得られた実施例1および比較例1〜2の塩
化ビニル樹脂加工布を下記組成の汚れコンパウンド中に
投入し,100回/日の攪拌を行ない,温度83℃の恒
温槽に6ケ月間放置した。また,耐洗濯性を検討するた
め,洗濯10洗後も同様な試験をした。さらに,3年間
屋外曝露を行った。各々の試料の汚れ状態をテイツシユ
・ペーパーでのふきとり後および水洗後の表面観察結果
を表1に示した。
〔汚れコンパウンド組成〕
ピートモス 38重量%セ
メント 17重量%カ
オリンクレー 17重量%シリカゲ
ル 17重量%カーボンブ
ラツク 1.75重量%酸化鉄
0.5 重量
%鉱 油(A重油) 8.75重
量%The obtained vinyl chloride resin-treated cloths of Example 1 and Comparative Examples 1 and 2 were placed in a stain compound having the following composition, stirred 100 times/day, and kept in a constant temperature bath at a temperature of 83° C. for 6 months. I left it for a while. In addition, in order to examine washing resistance, a similar test was conducted after 10 washes. Furthermore, outdoor exposure was performed for 3 years. Table 1 shows the surface observation results of each sample after wiping with tissue paper and washing with water. [Stain compound composition] Peat moss 38% by weight Cement 17% by weight Kaolin clay 17% by weight Silica gel 17% by weight Carbon black 1.75% by weight Iron oxide
0.5% by weight Mineral oil (heavy oil A) 8.75% by weight
【0020】[0020]
【表1】[Table 1]
【0021】表1より明らかなように,実施例1の塩化
ビニル樹脂加工布は,比較例1〜2に比べて優れた防汚
性を有し,かつ耐久性をも備えているものであった。[0021] As is clear from Table 1, the vinyl chloride resin-treated fabric of Example 1 has superior stain resistance and durability compared to Comparative Examples 1 and 2. Ta.
【0022】[0022]
【発明の効果】本発明は,塩化ビニル系樹脂を主成分と
する加工剤にて被覆されている布帛に,フルオロオレフ
インとアルキルビニルエーテル共重合体を主体とした重
合物を含有する溶剤系フツ素樹脂により被覆架橋化処理
をしているので,表面に汚れが付着しにくく,付着して
も取りやすい。また,塩化ビニル系樹脂表面の耐水圧を
向上させるので,水分の樹脂内への侵入を防止し樹脂層
の耐久性を増強させる。以上の如く本発明ば,耐久性の
ある,広い分野で利用できる防汚性塩化ビニル樹脂加工
布を提供できるものである。Effects of the Invention The present invention provides a method for applying a solvent-based fluorine containing a polymer mainly composed of a fluoroolefin and an alkyl vinyl ether copolymer to a fabric coated with a finishing agent mainly composed of a vinyl chloride resin. Since it is coated with resin and cross-linked, it is difficult for dirt to adhere to the surface, and even if it does, it is easy to remove. It also improves the water pressure resistance of the surface of the vinyl chloride resin, thereby preventing moisture from entering the resin and increasing the durability of the resin layer. As described above, the present invention can provide a stain-resistant vinyl chloride resin-treated cloth that is durable and can be used in a wide range of fields.
Claims (1)
剤にて被覆されている加工布であって、その被覆面にフ
ルオロオレフインとアルキルビニルエーテルの共重合体
を主体とした溶剤系弗素樹脂による被覆,架橋化処理が
施されてなることを特徴とする塩化ビニル樹脂加工布。Claim 1: A processed cloth coated with a finishing agent mainly composed of vinyl chloride resin, the coated surface of which is coated with a solvent-based fluororesin mainly composed of a copolymer of fluoroolefin and alkyl vinyl ether. A vinyl chloride resin-treated cloth characterized by being coated and crosslinked.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3223791A JPH04245976A (en) | 1991-01-31 | 1991-01-31 | Textile treated with vinyl chloride resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3223791A JPH04245976A (en) | 1991-01-31 | 1991-01-31 | Textile treated with vinyl chloride resin |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04245976A true JPH04245976A (en) | 1992-09-02 |
Family
ID=12353379
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3223791A Pending JPH04245976A (en) | 1991-01-31 | 1991-01-31 | Textile treated with vinyl chloride resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04245976A (en) |
-
1991
- 1991-01-31 JP JP3223791A patent/JPH04245976A/en active Pending
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