JPH09268472A - Cloth of dirt resistant polyester-based fiber and production of the same - Google Patents
Cloth of dirt resistant polyester-based fiber and production of the sameInfo
- Publication number
- JPH09268472A JPH09268472A JP7040596A JP7040596A JPH09268472A JP H09268472 A JPH09268472 A JP H09268472A JP 7040596 A JP7040596 A JP 7040596A JP 7040596 A JP7040596 A JP 7040596A JP H09268472 A JPH09268472 A JP H09268472A
- Authority
- JP
- Japan
- Prior art keywords
- cloth
- glycol
- block copolymer
- based fiber
- polyester fiber
- 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
- 239000004744 fabric Substances 0.000 title claims abstract description 33
- 239000000835 fiber Substances 0.000 title claims abstract description 26
- 229920000728 polyester Polymers 0.000 title claims abstract description 25
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 229920001400 block copolymer Polymers 0.000 claims abstract description 17
- 229920005989 resin Polymers 0.000 claims abstract description 17
- 239000011347 resin Substances 0.000 claims abstract description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000007788 liquid Substances 0.000 claims abstract description 15
- -1 alkylene glycol Chemical compound 0.000 claims abstract description 14
- 229920003180 amino resin Polymers 0.000 claims abstract description 11
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 10
- 125000003118 aryl group Chemical group 0.000 claims abstract description 10
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229920001515 polyalkylene glycol Polymers 0.000 claims abstract description 10
- 239000006185 dispersion Substances 0.000 claims abstract description 6
- 238000010438 heat treatment Methods 0.000 claims description 20
- 230000003373 anti-fouling effect Effects 0.000 claims description 12
- 229920000877 Melamine resin Polymers 0.000 abstract description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract description 6
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 abstract description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 abstract description 6
- 239000004640 Melamine resin Substances 0.000 abstract description 5
- 229920001577 copolymer Polymers 0.000 abstract description 4
- 125000005907 alkyl ester group Chemical group 0.000 abstract description 3
- 239000000463 material Substances 0.000 abstract description 3
- 239000002202 Polyethylene glycol Substances 0.000 abstract description 2
- 229920001223 polyethylene glycol Polymers 0.000 abstract description 2
- 229920001451 polypropylene glycol Polymers 0.000 abstract description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- 239000012209 synthetic fiber Substances 0.000 description 4
- 229920002994 synthetic fiber Polymers 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000003344 environmental pollutant Substances 0.000 description 2
- 231100000719 pollutant Toxicity 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- XYOSFLPUWVWHOA-UHFFFAOYSA-N 2-ethylidenepropane-1,3-diol;urea Chemical compound NC(N)=O.CC=C(CO)CO XYOSFLPUWVWHOA-UHFFFAOYSA-N 0.000 description 1
- DNPHEDNKXRMPAX-UHFFFAOYSA-N 3-hydroxypropylurea Chemical compound NC(=O)NCCCO DNPHEDNKXRMPAX-UHFFFAOYSA-N 0.000 description 1
- ZEYUSQVGRCPBPG-UHFFFAOYSA-N 4,5-dihydroxy-1,3-bis(hydroxymethyl)imidazolidin-2-one Chemical compound OCN1C(O)C(O)N(CO)C1=O ZEYUSQVGRCPBPG-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000011398 Portland cement Substances 0.000 description 1
- USDJGQLNFPZEON-UHFFFAOYSA-N [[4,6-bis(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(NCO)=NC(NCO)=N1 USDJGQLNFPZEON-UHFFFAOYSA-N 0.000 description 1
- YGCOKJWKWLYHTG-UHFFFAOYSA-N [[4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]-(hydroxymethyl)amino]methanol Chemical compound OCN(CO)C1=NC(N(CO)CO)=NC(N(CO)CO)=N1 YGCOKJWKWLYHTG-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 238000012661 block copolymerization Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000009990 desizing Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
- 229950005308 oxymethurea Drugs 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は洗濯耐久性のある黒
ずみ汚れ防止性能を有する防汚性ポリエステル系繊維布
帛およびその製造方法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an antifouling polyester fiber fabric having wash durability and anti-darkening stain performance, and a method for producing the same.
【0002】[0002]
【従来の技術】従来、防汚性合成繊維布帛と呼ばれるも
のは数多く提案されている。例えば、特公昭64−63
10号公報に記載されているようにフッ素化合物を含む
原糸油剤を合成繊維に付着させたり、特公昭64−27
08号公報に示されるようにフッ素系樹脂を繊維製品に
付着させたりして撥水溌油性を付与し、汚れの付着を防
止する方法や特公昭63−3078号公報に示されるよ
うにフッ素系樹脂と親水性ポリマを併用して防汚性を付
与する方法等が知られている。しかし、黒ずみ汚れ防止
に大きな効果があり、しかも洗濯耐久性を満足するもの
は見当たらなかった。2. Description of the Related Art Hitherto, many so-called antifouling synthetic fiber fabrics have been proposed. For example, Japanese Patent Publication No. 64-63
As described in Japanese Patent Publication No. 10, a raw yarn oil agent containing a fluorine compound is attached to a synthetic fiber, or Japanese Patent Publication No. 64-27.
As disclosed in Japanese Patent Publication No. 08-08, a method of imparting water-repellent and oil-repelling property by attaching a fluorine-based resin to a textile product, and a method of preventing the attachment of dirt are disclosed in Japanese Patent Publication No. 63-3078. A method of providing antifouling property by using a resin and a hydrophilic polymer in combination is known. However, none of them has a great effect on preventing darkening stains and has satisfactory washing durability.
【0003】[0003]
【発明が解決しようとする課題】本発明の目的は、洗濯
耐久性のある黒ずみ汚れ防止性能を有する防汚性ポリエ
ステル系繊維布帛およびその製造方法を提供することに
ある。SUMMARY OF THE INVENTION An object of the present invention is to provide an antifouling polyester fiber cloth having wash durability and anti-darkening stain resistance, and a method for producing the same.
【0004】[0004]
【問題を解決するための手段】本発明の防汚性ポリエス
テル系繊維布帛は、前記課題を解決するため次の構成を
有する。The antifouling polyester fiber cloth of the present invention has the following constitution in order to solve the above problems.
【0005】すなわち、ポリアルキレングリコール、芳
香族ジカルボン酸およびアルキレングリコールのブロッ
ク共重合体ならびに変性オルガノシリケート、アミノプ
ラスト樹脂が付着されてなることを特徴とする防汚性ポ
リエステル系繊維布帛である。That is, there is provided an antifouling polyester fiber cloth comprising a polyalkylene glycol, a block copolymer of an aromatic dicarboxylic acid and an alkylene glycol, a modified organosilicate, and an aminoplast resin.
【0006】また、本発明の防汚性ポリエステル系繊維
布帛の製造方法は前記課題を解決するため次の構成を有
する。Further, the method for producing an antifouling polyester fiber cloth of the present invention has the following constitution in order to solve the above problems.
【0007】すなわち、ポリアルキレングリコール、芳
香族ジカルボン酸およびアルキレングリコールのブロッ
ク共重合体を含む水分散液中で加熱処理後、変性オルガ
ノシリケートおよびアミノプラスト樹脂を含む処理液を
付与し、熱処理することを特徴とする防汚性ポリエステ
ル系繊維布帛の製造方法である。That is, after heat treatment in an aqueous dispersion containing a block copolymer of polyalkylene glycol, aromatic dicarboxylic acid and alkylene glycol, a treatment liquid containing modified organosilicate and aminoplast resin is applied and heat treated. And a method for producing an antifouling polyester fiber cloth.
【0008】[0008]
【発明の実施の形態】以下、本発明を詳細に説明する。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below.
【0009】本発明にかかるポリエステル系繊維布帛と
は、ポリエチレンテレフタレート、ポリブチレンテレフ
タレートやこれらを主成分とした共重合体のポリエステ
ル系繊維を含む織物、編物、不織布などのことをいい、
ポリエステル系繊維以外の合成繊維や再生繊維あるいは
天然繊維が混紡、混繊されて含まれていてもよい。The polyester fiber cloth according to the present invention refers to a woven fabric, a knitted fabric, a non-woven fabric, etc. containing polyethylene terephthalate, polybutylene terephthalate or a polyester fiber of a copolymer containing these as a main component,
Synthetic fibers other than polyester fibers, regenerated fibers or natural fibers may be mixed and mixed and included.
【0010】本発明で用いるポリアルキレングリコール
とは、分子中に−(CHO)−(n=2〜4)なる主鎖
を有するもののことをいい、分子量が300〜4000
0の範囲にあるのが好ましく、より好ましくは1000
〜10000の範囲である。例えばポリエチレングリコ
ール、ポリプロピレングリコールまたはこれらのブロッ
クポリマ等を使用することができる。分子量が300に
満たないと耐久性が不十分となる傾向があり、分子量が
40000を越えると分散性が低下する傾向がある。The polyalkylene glycol used in the present invention is one having a main chain of-(CHO)-(n = 2-4) in the molecule, and has a molecular weight of 300-4000.
It is preferably in the range of 0, and more preferably 1000.
The range is from 10,000 to 10,000. For example, polyethylene glycol, polypropylene glycol or block polymers thereof can be used. If the molecular weight is less than 300, the durability tends to be insufficient, and if the molecular weight exceeds 40,000, the dispersibility tends to decrease.
【0011】芳香族ジカルボン酸とは、例えばテレフタ
ル酸またはテレフタル酸の低級アルキルエステルおよび
イソフタル酸のうち少なくともいずれかまたはイソフタ
ル酸の低級アルキルエステルのことをいう。The aromatic dicarboxylic acid means, for example, terephthalic acid or at least one of lower alkyl ester of terephthalic acid and isophthalic acid, or lower alkyl ester of isophthalic acid.
【0012】アルキレングリコールとは、下記一般式
[I ]で表されるものであり、例えばエチレングリコー
ル、プロピレングリコール、ブチレングリコールなどを
用いることができる。The alkylene glycol is represented by the following general formula [I], and for example, ethylene glycol, propylene glycol, butylene glycol and the like can be used.
【0013】[0013]
【化1】 (n=2〜4) ポリアルキレングリコール、芳香族ジカルボン酸および
アルキレングリコールのブロック共重合体において各々
のブロック共重合モル比は、1〜31:1:2〜3のも
のが防汚性の面から見て好ましい。該ブロック共重合体
は、ノニオン系またはアニオン系の界面活性剤を用いて
水に分散させて用いるとよい。該ブロック共重合体を含
む水分散液中での処理温度は80〜140℃の範囲が好
ましい。処理時間は、通常3分から30分位で十分であ
る。該ブロック共重合体による処理は、染色と同時に行
なうことができる。すなわち、染料と該ブロック共重合
体を併用して通常のポリエステル系繊維の染色条件で処
理することが可能である。なお、該ブロック共重合体に
よる処理に先立ち、生地の風合いを柔らかくするため苛
性ソーダなどのアルカリ剤によるポリエステルの減量加
工を行なうことは好ましい。Embedded image (N = 2 to 4) In the block copolymer of polyalkylene glycol, aromatic dicarboxylic acid and alkylene glycol, the block copolymerization molar ratio of 1 to 3: 1: 2 to 3 is the antifouling property. It is preferable from the viewpoint. The block copolymer is preferably used by dispersing it in water using a nonionic or anionic surfactant. The treatment temperature in the aqueous dispersion containing the block copolymer is preferably in the range of 80 to 140 ° C. Processing time of about 3 minutes to 30 minutes is usually sufficient. The treatment with the block copolymer can be performed simultaneously with the dyeing. That is, it is possible to use a dye and the block copolymer in combination and to treat the polyester fiber under ordinary dyeing conditions. Prior to the treatment with the block copolymer, it is preferable to reduce the weight of the polyester with an alkaline agent such as caustic soda in order to soften the texture of the dough.
【0014】該ブロック共重合体は、合成繊維布帛重量
に対し、0.02〜5重量%付与されるのが好ましく、
0.1〜3重量%付与されるのがより好ましい。該共重
合体を含む水分散液中でのポリエステル系繊維布帛の加
熱処理は、変性オルガノシリケートおよびアミノプラス
ト樹脂を含む処理液を付与する前に行われる必要があ
る。変性オルガノシリケートおよびアミノプラスト樹脂
を含む処理液を付与後に、共重合体を含む水分散液中で
のポリエステル系繊維布帛の加熱処理を施すと、黒ずみ
汚れ防止性能が発現され得ないという問題がある。The block copolymer is preferably added in an amount of 0.02 to 5% by weight, based on the weight of the synthetic fiber cloth.
More preferably, 0.1 to 3% by weight is applied. The heat treatment of the polyester fiber cloth in the aqueous dispersion containing the copolymer needs to be performed before applying the treatment liquid containing the modified organosilicate and the aminoplast resin. If a polyester fiber fabric is heat-treated in an aqueous dispersion containing a copolymer after a treatment liquid containing a modified organosilicate and an aminoplast resin is applied, there is a problem that the darkening stain prevention performance cannot be exhibited. .
【0015】また、該ブロック共重合体の付与量が0.
02重量%以下では黒ずみ汚れ防止性が十分に発現され
ない傾向であり、5重量%以上では生地の風合いが堅く
なり、染色堅牢度も低下する傾向にある。The amount of the block copolymer added is 0.
If it is less than 02% by weight, the dark stain resistance is not sufficiently exhibited, and if it is more than 5% by weight, the texture of the fabric tends to be hard and the dyeing fastness tends to be low.
【0016】本発明で用いる変性オルガノシリケート
は、下記一般式[II]で表される。The modified organosilicate used in the present invention is represented by the following general formula [II].
【0017】[0017]
【化2】 (R:CH3 、C2 H5 などのアルキル基を表わす) 変性オルガノシリケートは、ポリエステル系繊維布帛重
量に対し、0.01〜5重量%付与されるのが好まし
く、0.1〜3重量%付与されるのがより好ましい。
0.01重量%より小さいと黒ずみ汚れ防止性能が不十
分となる傾向があり、5重量%より大きいと風合いが損
なわれる傾向がある。Embedded image (R: CH 3, alkyl group represents a such C 2 H 5) modified organosilicate, compared polyester fiber fabric weight is preferably is 0.01 to 5 wt% grant, 0.1-3 % Is more preferable.
If it is less than 0.01% by weight, the dark stain prevention performance tends to be insufficient, and if it is more than 5% by weight, the texture tends to be impaired.
【0018】本発明で用いるアミノプラスト樹脂として
は、例えばトリメチロールメラミン、ヘキサメチロール
メラミンなどのメラミン樹脂、ジメチロール尿素、ジメ
チロールジヒドロキシエチレン尿素、ジメチルジヒドロ
キシエチレン尿素、ジメチロールジメトキシエチレン尿
素、ジメチロールブチレン尿素、ジメチロールプロピレ
ン尿素、ジメチロール5ヒドロキシプロピル尿素などの
尿素樹脂、ジメチロールウロンなどのウロン系樹脂など
を用いることができる。アミノプラスト樹脂は、ポリエ
ステル系繊維布帛重量に対し、0.01〜5重量%付与
されるのが好ましい。0.01重量%より小さいと黒ず
み汚れ防止性能の洗濯耐久性が不十分となる傾向があ
り、5重量%より大きいと風合いが粗硬になる傾向があ
る。Examples of the aminoplast resin used in the present invention include melamine resins such as trimethylolmelamine and hexamethylolmelamine, dimethylolurea, dimethyloldihydroxyethyleneurea, dimethyldihydroxyethyleneurea, dimethyloldimethoxyethyleneurea and dimethylolbutyleneurea. It is possible to use urea resins such as dimethylol propylene urea and dimethylol 5 hydroxypropyl urea, and uronic resins such as dimethyloluron. The aminoplast resin is preferably added in an amount of 0.01 to 5% by weight based on the weight of the polyester fiber cloth. If it is less than 0.01% by weight, the washing durability of dark stain prevention performance tends to be insufficient, and if it is more than 5% by weight, the texture tends to be coarse and hard.
【0019】変性オルガノシリケートおよびアミノプラ
スト樹脂を含む処理液のポリエステル系繊維布帛に対す
る付与方法としては、パッディング、浸漬法、スプレー
方式、コーティング方式などを採用することができる。
本発明でいう熱処理とは、乾熱処理または湿熱処理のこ
とをいう。湿熱処理には浴中処理とスチーム処理が含ま
れる。スチーム処理には、常圧飽和スチーム処理、過熱
スチーム処理、高圧スチーム処理などを採用することが
できる。乾熱処理または湿熱処理の温度は100〜21
0℃位が好ましい。熱処理温度が100℃以下であると
洗濯耐久性の面で不十分となる傾向にあり、一方、21
0℃を越えると繊維の黄化、脆化が生じる傾向にある。As a method for applying the treatment liquid containing the modified organosilicate and the aminoplast resin to the polyester fiber cloth, padding, dipping, spraying, coating or the like can be adopted.
The heat treatment in the present invention means dry heat treatment or wet heat treatment. The moist heat treatment includes in-bath treatment and steam treatment. As the steam treatment, a normal pressure saturated steam treatment, a superheated steam treatment, a high pressure steam treatment and the like can be adopted. The temperature of dry heat treatment or wet heat treatment is 100 to 21.
About 0 ° C is preferable. When the heat treatment temperature is 100 ° C or lower, the washing durability tends to be insufficient, while
If the temperature exceeds 0 ° C, the fibers tend to be yellowed and brittle.
【0020】以下、本発明を実施例によりさらに詳細に
説明する。なお、実施例中の性能評価はつぎの方法で行
った。Hereinafter, the present invention will be described in more detail with reference to Examples. In addition, the performance evaluation in an Example was performed by the following method.
【0021】〔黒ずみ汚れ防止性能〕 手順1:ポリエチレン袋(20l)に100℃×2時間
乾燥させた汚染剤A0.2g、タテ10cm、ヨコ15
cmのサンプルとICIピリング用ゴム管1本を入れ
る。20℃×65%RHの空気で袋を膨らまし輪ゴムで
止める(約10l)。[Black stain prevention performance] Step 1: 0.2 g of a pollutant A dried in a polyethylene bag (20 l) at 100 ° C. for 2 hours, vertical 10 cm, horizontal 15
cm sample and a rubber tube for ICI pilling. Inflate the bag with air at 20 ° C. × 65% RH and stop with a rubber band (about 10 l).
【0022】手順2:手順1のポリエチレン袋をICI
試験機の箱に入れ1時間回転処理をする。理サンプルを
取り出す。Step 2: ICI the polyethylene bag of step 1
Put in the box of the tester and rotate for 1 hour. Take out a physical sample.
【0023】手順3:処理サンプルを標準洗濯条件で1
回洗浄する。手順1〜手順3をさらに2回繰り返す。Step 3: Treated sample 1 under standard wash conditions
Wash twice. Repeat steps 1 to 3 two more times.
【0024】手順4:上記のとおり汚染剤付着・洗浄を
3回繰り返したサンプルと未処理のサンプルのL値を測
色計で測定し、△L値を計算する。Step 4: The L value of the sample in which the contaminants are attached and washed three times as described above and the untreated sample are measured with a colorimeter, and the ΔL value is calculated.
【0025】 〔汚染剤A〕 薬 品 名 組成(重量%) 規 格 粘土 55 信楽粘土を乳鉢ですりつぶしたもの ポルトランドセメント 17 JIS R5210 二酸化ケイ素 17 JIS K8885 酸化第2鉄 0.5 試薬CP級のもの n−デカン 8.75 試薬EP級のもの カーボンブラック 1.75 玉川カーボンブラック 〔標準洗濯条件〕 洗い:ザブ2g/l、4℃×5分 すすぎ:常温水、オーバーフロー2分×2回 乾燥:タンブラー30分 実施例中の生地は、ポリエステル織物(東レ株式会社製
#1413、タテ糸75D−36fil ヨコ糸75D
−72fil)を用いた。[Pollutant A] Drug name Composition (wt%) Standard clay 55 Shigaraki clay ground in a mortar Portland cement 17 JIS R5210 Silicon dioxide 17 JIS K8885 Ferric oxide 0.5 Reagent CP grade n-decane 8.75 Reagent EP grade carbon black 1.75 Tamagawa carbon black [Standard washing conditions] Washing: Zab 2g / l, 4 ° C x 5 minutes Rinse: room temperature water, overflow 2 minutes x 2 times Drying: tumbler 30 minutes The fabric in the examples is a polyester woven fabric (# 1413 manufactured by Toray Industries Inc., vertical thread 75D-36fil horizontal thread 75D).
-72 fil) was used.
【0026】上記生地を通常の方法で糊抜き精練、乾熱
セット後、試験に供した。The above dough was subjected to desizing and scouring by a conventional method, set to dry heat, and then subjected to a test.
【0027】[実施例1]供試生地をポリアルキレング
リコール、芳香族ジカルボン酸およびアルキレングリコ
ールのブロック共重合体TO−SR−1(高松油脂株式
会社製、固形分10%)7%owfを含み酢酸でPH
4.5に調整した処理液に投入し130℃×15分処理
後、水洗、乾燥した。得られた生地を下記組成の処理液
に浸漬後、マングルで絞り(ピックアップ60%)、1
20℃×3分で乾熱処理後、ピンテンターで190℃×
1分乾熱処理を行い、評価に供した。結果を表1に示
す。[Example 1] The test fabric contains 7% owf of polyalkylene glycol, aromatic dicarboxylic acid and alkylene glycol block copolymer TO-SR-1 (manufactured by Takamatsu Yushi Co., Ltd., solid content 10%). PH with acetic acid
The mixture was added to the treatment liquid adjusted to 4.5, treated at 130 ° C. for 15 minutes, washed with water and dried. After soaking the obtained dough in the treatment liquid of the following composition, squeezing with a mangle (pickup 60%), 1
After dry heat treatment at 20 ℃ × 3 minutes, 190 ℃ × with a pin tenter
It was subjected to a dry heat treatment for 1 minute and provided for evaluation. The results are shown in Table 1.
【0028】変性オルガノシリケート:H−3669−
2NI(高松油脂株式会社製)30g/l メラミン樹脂:スミテックスレジンMK(住友化学工業
株式会社製)3g/l 触媒:カタリストRC−W(株式会社京絹化成製)2g
/lModified organosilicate: H-3669-
2NI (manufactured by Takamatsu Yushi Co., Ltd.) 30 g / l Melamine resin: Sumitex resin MK (manufactured by Sumitomo Chemical Co., Ltd.) 3 g / l Catalyst: Catalyst RC-W (manufactured by Kyokushin Kasei Co., Ltd.) 2 g
/ L
【表1】 [実施例2]供試生地をポリアルキレングリコール、芳
香族ジカルボン酸およびアルキレングリコールのブロッ
ク共重合体TO−SR−1(高松油脂株式会社製、固形
分10%)3%owfを含み酢酸でPH4.5に調整し
た処理液に投入し130℃×15分処理した。得られた
生地を下記組成の処理液に浸漬後、マングルで絞り(ピ
ックアップ60%)、105℃×3分でスチーム処理
後、120℃×3分乾熱処理を行い、評価に供した。結
果を表1に示す。[Table 1] [Example 2] The test fabric contains 3% owf of polyalkylene glycol, aromatic dicarboxylic acid and alkylene glycol block copolymer TO-SR-1 (manufactured by Takamatsu Yushi Co., Ltd., solid content 10%), and PH4 with acetic acid. The mixture was added to the treatment solution adjusted to 0.5 and treated at 130 ° C. for 15 minutes. The obtained dough was dipped in a treatment liquid having the following composition, squeezed with a mangle (pickup 60%), steamed at 105 ° C. for 3 minutes, and dried at 120 ° C. for 3 minutes, and subjected to evaluation. The results are shown in Table 1.
【0029】変性オルガノシリケート:H−3669−
2NI(高松油脂株式会社製)30g/l メラミン樹脂:スミテックスレジンM−3(住友化学工
業株式会社製)30g/l 触媒:過硫酸アンモニウム2g/l [実施例3]供試生地をポリアルキレングリコール、芳
香族ジカルボン酸およびアルキレングリコールのブロッ
ク共重合体TO−SR−1(高松油脂株式会社製、固形
分10%)10%owfを含み酢酸でPH4.5に調整
した処理液に投入し130℃×15分処理した。得られ
た生地を下記組成の処理液に浸漬後、マングルで絞り
(ピックアップ60%)、120℃×3分で乾熱処理
後、ピンテンターで180℃×1分乾熱処理を行い評価
に供した。結果を表1に示す。Modified organosilicate: H-3669-
2NI (manufactured by Takamatsu Oil & Fat Co., Ltd.) 30 g / l Melamine resin: Sumitex Resin M-3 (manufactured by Sumitomo Chemical Co., Ltd.) 30 g / l Catalyst: Ammonium persulfate 2 g / l [Example 3] Polyalkylene glycol , A block copolymer of aromatic dicarboxylic acid and alkylene glycol TO-SR-1 (manufactured by Takamatsu Yushi Co., Ltd., solid content 10%) containing 10% owf, added to a treatment liquid adjusted to pH 4.5 with acetic acid and put at 130 ° C. × 15 minutes treatment. The obtained fabric was dipped in a treatment liquid having the following composition, squeezed with a mangle (pickup 60%), subjected to dry heat treatment at 120 ° C. for 3 minutes, and then subjected to dry heat treatment at 180 ° C. for 1 minute with a pin tenter for evaluation. The results are shown in Table 1.
【0030】変性オルガノシリケート:H−3669−
2NI(高松油脂株式会社製)10g/l 尿素樹脂:スミテックスレジン(住友化学工業株式会社
製)30g/l NF−500K 触媒:スミテックスACC.ACX 2g/l [比較例1]供試生地を実施例1と同様にTO−SR−
1で処理し評価に供した。結果を表1に示す。Modified organosilicate: H-3669-
2NI (manufactured by Takamatsu Yushi Co., Ltd.) 10 g / l Urea resin: Sumitex resin (manufactured by Sumitomo Chemical Co., Ltd.) 30 g / l NF-500K Catalyst: Sumitex ACC. ACX 2 g / l [Comparative Example 1] The same as in Example 1 was used for TO-SR-
It processed with 1 and used for evaluation. The results are shown in Table 1.
【0031】[比較例2]供試生地を実施例1と同様に
TO−SR−1で処理した。得られた生地を下記組成の
処理液に浸漬後、マングルで絞り(ピックアップ60
%)、120℃×3分で乾熱処理後、ピンテンターで1
90℃×1分乾熱処理を行い、評価に供した。結果を表
1に示す。[Comparative Example 2] The test material was treated with TO-SR-1 in the same manner as in Example 1. After dipping the obtained dough in the treatment liquid of the following composition, squeeze it with a mangle (pickup 60
%), After dry heat treatment at 120 ° C x 3 minutes, 1 with a pin tenter
It was subjected to dry heat treatment at 90 ° C. for 1 minute and provided for evaluation. The results are shown in Table 1.
【0032】メラミン樹脂:スミテックスレジンMK
(住友化学工業株式会社製)3g/l 触媒:カタリストRC−W(株式会社京絹化成製)2g
/l [比較例3]供試生地を実施例1と同様にTO−SR−
1で処理した。得られた生地を下記組成の処理液に浸漬
後、マングルで絞り(ピックアップ60%)、120℃
×3分で乾熱処理後、ピンテンターで190℃×1分乾
熱処理を行い、評価に供した。結果を表1に示す。Melamine resin: Sumitex resin MK
(Sumitomo Chemical Co., Ltd.) 3 g / l Catalyst: Catalyst RC-W (Kyokin Chemical Co., Ltd.) 2 g
/ L [Comparative Example 3] The sample fabric was TO-SR-
Processed in 1. After soaking the obtained dough in the treatment liquid of the following composition, squeezing with a mangle (pickup 60%), 120 ° C
After dry heat treatment at × 3 minutes, a dry heat treatment was performed at 190 ° C. for 1 minute with a pin tenter, and the resultant was evaluated. The results are shown in Table 1.
【0033】変性オルガノシリケート:H−3669−
2NI(高松油脂株式会社製)30g/l [比較例4]供試生地を下記組成の処理液に浸漬後、マ
ングルで絞り(ピックアップ60%)、120℃×3分
で乾熱処理後、ピンテンターで190℃×1分乾熱処理
を行い、評価に供した。結果を表1に示す。Modified organosilicate: H-3669-
2NI (manufactured by Takamatsu Yushi Co., Ltd.) 30 g / l [Comparative Example 4] After dipping the test material in the treatment liquid having the following composition, squeezing with a mangle (pickup 60%), dry heat treatment at 120 ° C for 3 minutes, and then with a pin tenter It was subjected to dry heat treatment at 190 ° C. for 1 minute and provided for evaluation. The results are shown in Table 1.
【0034】変性オルガノシリケート:H−3669−
2NI(高松油脂株式会社製)30g/l メラミン樹脂:スミテックスレジンMK(住友化学工業
株式会社製)3g/l 架橋剤:カタリストRC−W(株式会社京絹化成製)2
g/lModified organosilicate: H-3669-
2NI (manufactured by Takamatsu Oil & Fat Co., Ltd.) 30 g / l Melamine resin: Sumitex Resin MK (manufactured by Sumitomo Chemical Co., Ltd.) 3 g / l Crosslinking agent: Catalyst RC-W (manufactured by Kyokushin Kasei Co., Ltd.) 2
g / l
【0035】[0035]
【発明の効果】本発明によれば耐久性のある黒ずみ汚れ
防止性能を有する防汚性ポリエステル系繊維布帛が得ら
れる。また、該布帛は吸水性、帯電防止性の向上にも効
果がある。EFFECTS OF THE INVENTION According to the present invention, an antifouling polyester fiber cloth having a durable performance for preventing darkening stains can be obtained. The cloth is also effective in improving water absorption and antistatic properties.
Claims (2)
ボン酸およびアルキレングリコールのブロック共重合体
ならびに変性オルガノシリケート、アミノプラスト樹脂
が付着されてなることを特徴とする防汚性ポリエステル
系繊維布帛。1. An antifouling polyester fiber cloth comprising a block copolymer of polyalkylene glycol, an aromatic dicarboxylic acid and an alkylene glycol, a modified organosilicate, and an aminoplast resin attached thereto.
ボン酸およびアルキレングリコールのブロック共重合体
を含む水分散液中で加熱処理後、変性オルガノシリケー
トおよびアミノプラスト樹脂を含む処理液を付与し、熱
処理することを特徴とする防汚性ポリエステル系繊維布
帛の製造方法。2. After heat treatment in an aqueous dispersion containing a block copolymer of polyalkylene glycol, aromatic dicarboxylic acid and alkylene glycol, a treatment liquid containing modified organosilicate and aminoplast resin is applied and heat treated. A method for producing an antifouling polyester-based fiber cloth.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7040596A JPH09268472A (en) | 1996-03-26 | 1996-03-26 | Cloth of dirt resistant polyester-based fiber and production of the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7040596A JPH09268472A (en) | 1996-03-26 | 1996-03-26 | Cloth of dirt resistant polyester-based fiber and production of the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH09268472A true JPH09268472A (en) | 1997-10-14 |
Family
ID=13430533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7040596A Pending JPH09268472A (en) | 1996-03-26 | 1996-03-26 | Cloth of dirt resistant polyester-based fiber and production of the same |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH09268472A (en) |
-
1996
- 1996-03-26 JP JP7040596A patent/JPH09268472A/en active Pending
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