JPH028068B2 - - Google Patents
Info
- Publication number
- JPH028068B2 JPH028068B2 JP57187385A JP18738582A JPH028068B2 JP H028068 B2 JPH028068 B2 JP H028068B2 JP 57187385 A JP57187385 A JP 57187385A JP 18738582 A JP18738582 A JP 18738582A JP H028068 B2 JPH028068 B2 JP H028068B2
- Authority
- JP
- Japan
- Prior art keywords
- fabric
- acid
- coating
- resin
- present
- 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.)
- Expired - Lifetime
Links
- 239000004744 fabric Substances 0.000 claims description 29
- 238000000576 coating method Methods 0.000 claims description 12
- 239000011248 coating agent Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 238000011282 treatment Methods 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 3
- 230000005494 condensation Effects 0.000 claims description 3
- 239000000975 dye Substances 0.000 description 12
- 229920002994 synthetic fiber Polymers 0.000 description 10
- 239000012209 synthetic fiber Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 238000011109 contamination Methods 0.000 description 6
- 238000013508 migration Methods 0.000 description 6
- 230000005012 migration Effects 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- -1 fatty acid carboxylic acids Chemical class 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000006482 condensation reaction Methods 0.000 description 2
- 238000000280 densification Methods 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920001007 Nylon 4 Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920006280 packaging film Polymers 0.000 description 1
- 239000012785 packaging film Substances 0.000 description 1
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Coloring (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
本発明は染色された布帛におけるコーテイング
加工方法に関する。更に詳しくは、染色された合
成繊維の移行汚染を防止したコーテイング加工方
法に関する。
合成繊維は種々のすぐれた物理的、化学的性質
を有し、衣料用、産業用資材として用いられてい
る。また、コーテイング加工の基布としてもすぐ
れた素材である。しかし、従来は合成繊維に染色
されている染料はコーテイングされた樹脂との相
溶性が大きいため、時間が経つにつれて繊維の中
の染料が次第に樹脂の中に溶け出して着色された
状態になり、さらにこの樹脂に溶け出した染料
が、別のコーテイング布帛を重ねて押えつけたま
ま長時間放置したりすると、両者の間に色移り現
象が発生することがあつた。また、貯蔵中の製品
においてその染料が包装フイルムを汚染し、さら
に他の製品をを汚染するといういわゆる染料の移
行汚染が発生することがあつた。
本発明者らは、合成繊維コーテイング加工品の
かかる欠点を解消すべく鋭意研究の結果、本発明
に到達したものである。
すなわち、本発明は染色された布帛に下記一般
式〔〕:
〔式中、R1〜R6はそれぞれ独立して−H、−OH、
−OCoH2o+1、−CH2OCoH2o+1、−CH2OH、−
CH2CH2OH、−CH2CH2CH2OH、−CONH2、−
CONHCH2OH又は
The present invention relates to a method for coating dyed fabrics. More specifically, the present invention relates to a coating method that prevents migration staining of dyed synthetic fibers. Synthetic fibers have various excellent physical and chemical properties and are used for clothing and industrial materials. It is also an excellent material as a base fabric for coating processes. However, conventionally, the dyes used to dye synthetic fibers have a high compatibility with the coated resin, so over time, the dyes in the fibers gradually dissolve into the resin and become colored. Furthermore, if the dye dissolved into the resin was left to stand for a long time while being pressed against another coated fabric, a color transfer phenomenon could occur between the two. In addition, dyes from stored products contaminate the packaging film and further contaminate other products, which is what is called dye transfer contamination. The present inventors have arrived at the present invention as a result of intensive research in order to eliminate such drawbacks of synthetic fiber coated products. That is, the present invention provides dyed fabric with the following general formula []: [In the formula, R 1 to R 6 are each independently -H, -OH,
−OC o H 2o+1 , −CH 2 OC o H 2o+1 , −CH 2 OH, −
CH2CH2OH , -CH2CH2CH2OH , -CONH2 , -
CONHCH 2 OH or
【式】を表わ
す。ここにnは整数を表わす。〕
で示される化合物を付与し、マイクロウエーブ加
熱により縮合処理した後、該布帛をコーテイング
処理することにより、染料の移行汚染を防止する
コーテイング加工方法に関する。
本発明において使用される合成繊維の例として
はナイロン4、ナイロン6、ナイロン66、ナイロ
ン610、ナイロン12あるいはこれらを構成するモ
ノマー単位の2種または2種以上からなる共重体
の如きポリアミド類、セバシン酸とエチレングリ
コール、アジピン酸とエチレングリコールあるい
はテルフタル酸とエチレングリコール又はブチレ
ングリコールとの縮合反応によつて生成されるポ
リエステル類、およびポリエステルとポリアミド
との複合体及びこれらを含む混紡あるいは交織繊
維等があげられるが、何らこれらに限定されるも
のではない。またこれらの合成繊維類の形態は綿
状、糸状、スライバー状、編織物状、不織布状等
のいかなる形態にあつてもよい。
本発明において〔〕式の化合物(メラミン樹
脂)は水溶液又は水分散液中0.01重量%以上の濃
度、特に0.05〜10重量%の濃度で用いられるのが
好ましい。合成繊維上に付着する樹脂量として
は、繊維重量に対して0.1重量%以上であるのが
好ましく、1〜10重量%の範囲が変色もなく、風
合も良好であり、特に好ましい。
本発明における式〔〕の化合物の縮合反応は
触媒の存在下におこなわれるのがよく、かかる触
媒としてはギ酸、酢酸などの脂肪酸カルボン酸、
アクリル酸などの飽和ジカルボン酸、リンゴ酸、
酒石酸などのオキシカルボン酸、グルタミン酸な
どのアミノカルボン酸、マレイン酸などの不飽和
ジカルボン酸、フタール酸などの芳香族ジカルボ
ン酸およびそれらのアンモニウム、ナトリウム、
カリウム等の塩があげられる。また、有機塩以外
には硫酸、過硫酸、塩酸、リン酸、硝酸などの無
機酸のアンモニウム、ナトリウム、マグネシウ
ム、アルミニウムなどの塩およびこれらの複塩が
あげられる。これらの触媒は0.01〜10重量%の範
囲の浴中濃度で用いられるのが好ましい。
これらの混合水溶液を付着させる方法として
は、浸漬、スプレー塗布、キスロールまたは転写
法等の任意の方法が用いられる。
混合水溶液付着後の縮合処理のためには、マイ
クロウエーブ加熱を利用する。つまり、マイクロ
波を使用することにより、式〔〕の化合物を含
浸させた合成繊維製品を布帛の内深部より均一に
加熱するものである。このマイクロウエーブ加熱
は。例えば、水分の存在下に、100W〜20kW、
好ましくは2〜10kWの出力において、10秒〜60
分間、好ましくは10〜30分間マイクロウエーブ照
射することにより行うことができる。また、本発
明において、混合水溶液の分散安定性のために、
界面活性剤を用いても何ら効果に影響はない。
これらの処理により、合成繊維表層部に厚さ
0.01ミクロン以上、好ましくは0.05〜10ミクロン
の皮膜を形成する。該皮膜は染料とは相溶性が悪
く、合成繊維表層部の染料が該皮膜表面上に出る
のを防止し、次いで加工されるコーテイング層の
中に染料が移行汚染するのを効果的に防止する。
即ち、本発明に従つてマイクロウエーブ加熱を行
うことにより、高エネルギー状態による水素引き
抜き反応等が起り易く、縮合生成物の架橋が促進
されて、得られるメラミン皮膜の緻密化が増大す
るために、堅牢度の飛躍的な向上が得られるので
あると思われる。
本発明における式〔〕の化合物の付与及び縮
合処理後のコーテイング加工については周知の任
意の方法が可能である。すなわち、湿式、乾式の
いずれのコーテイング方法も、あるいはウレタン
樹脂、アクリル樹脂等のいずれの樹脂処方も、ま
たナイフコーター、パイプコーター、リバースコ
ーター、キスロール等のいずれのコーテイング手
段の使用も可能である。
また、本発明によつて付与された移行汚染防止
効果は、家庭洗濯、ドライクリーニング等によつ
て失効するものではなく、効果の持続性は半永久
的である。また、従来の樹脂加工にみられる加工
布の風合の硬化はほとんど起こらず、良好な品位
を有している。
以下、実施例により本発明を更に説明する。
実施例 1
ポリエステルポンヂー織物(目付220g/m2)
を常法で糊抜き精練後、乾燥し、180℃で30秒間
熱処理する。次いで所定の染料、助剤、酢酸0.3
%を用い、浴比1:40において、130℃で60分染
色し、還元洗浄後、中和、水洗、乾燥する。つづ
いて下記処方の処理液中に浸漬し、絞り率60%に
絞つた後、100℃の飽和水蒸気を充填したマイク
ロウエーブ照射室内において、出力5kWで10分
間処理後、熱水で5分間ソーピングし、180℃で
30秒間乾熱セツトした。
樹脂処方
Sumitex Resin M−3(住友化学工業製) 5部
Sumitex Accellerator EPX(住友化学工業製)
0.5部
水を加えて全量を100部とする。
該染色処理布を基布として、ポリウレタン透明
ラミネートコーテイング加工を行ない、ポリウレ
タン層を20μmの厚さに塗布した。ラミネート樹
脂として、ワクスボン7367(大日本インキKK)
を使用した。
得られた試料の移行汚染を下記手順で調べた。
ポリエステルタフタ(さらし済)のウレタン
透明ラミネート品のウレタン面を試料のウレタ
ン面に合わせて添付し、汗試験器用のガラス板
2枚の間にはさみ、4.5Kgの荷重をかける。
80±2℃の乾燥機中に入れ、48時間放置す
る。
複合試験片を取り出し、室温まで放冷する。
試験後の添付布に見える汚染を汚染用グレース
ケールにより等級評価をした。さらに試料の未処
理品と処理後品との色差を評価した。これらの結
果を表1に示す。
表1より明らかなように、本発明による処理布
は著しい移行汚染防止効果を示し、また風合硬化
もなく良好なる品位を有していた。
尚、色差(ΔE)は未処理布と処理布との色差
を島津分光光度計カラーセブン(C光源、1976、
La※b※方式)により測定して求めた。Represents [formula]. Here n represents an integer. ] The present invention relates to a coating method for preventing dye transfer contamination by applying a compound represented by the following and condensing the fabric by microwave heating, and then coating the fabric. Examples of synthetic fibers used in the present invention include polyamides such as nylon 4, nylon 6, nylon 66, nylon 610, nylon 12, or copolymers consisting of two or more monomer units constituting these, and sebacine. Polyesters produced by the condensation reaction of acid and ethylene glycol, adipic acid and ethylene glycol, or terphthalic acid and ethylene glycol or butylene glycol, composites of polyester and polyamide, and blended or interwoven fibers containing these. However, it is not limited to these in any way. Further, these synthetic fibers may be in any form such as cotton, thread, sliver, knitted fabric, or nonwoven fabric. In the present invention, the compound of the formula (melamine resin) is preferably used in an aqueous solution or dispersion at a concentration of 0.01% by weight or more, particularly from 0.05 to 10% by weight. The amount of resin deposited on the synthetic fiber is preferably 0.1% by weight or more based on the weight of the fiber, and a range of 1 to 10% by weight is particularly preferred since no discoloration occurs and the texture is good. The condensation reaction of the compound of formula [] in the present invention is preferably carried out in the presence of a catalyst, and such catalysts include fatty acid carboxylic acids such as formic acid and acetic acid,
Saturated dicarboxylic acids such as acrylic acid, malic acid,
Oxycarboxylic acids such as tartaric acid, aminocarboxylic acids such as glutamic acid, unsaturated dicarboxylic acids such as maleic acid, aromatic dicarboxylic acids such as phthalic acid, and their ammonium, sodium,
Examples include salts such as potassium. In addition to organic salts, salts of inorganic acids such as sulfuric acid, persulfuric acid, hydrochloric acid, phosphoric acid, and nitric acid, such as ammonium, sodium, magnesium, and aluminum, and their double salts can be mentioned. These catalysts are preferably used at bath concentrations ranging from 0.01 to 10% by weight. Any method such as dipping, spray coating, kiss roll or transfer method can be used to apply the mixed aqueous solution. Microwave heating is used for condensation treatment after adhesion of the mixed aqueous solution. That is, by using microwaves, a synthetic fiber product impregnated with the compound of formula [] is uniformly heated from the deep inside of the fabric. This microwave heating. For example, in the presence of moisture, 100W to 20kW,
Preferably at an output of 2 to 10 kW, 10 seconds to 60
This can be carried out by microwave irradiation for minutes, preferably 10 to 30 minutes. In addition, in the present invention, for the dispersion stability of the mixed aqueous solution,
Even if a surfactant is used, the effect is not affected in any way. These treatments add thickness to the surface layer of synthetic fibers.
Form a film of 0.01 micron or more, preferably 0.05 to 10 micron. The film has poor compatibility with dyes, and prevents the dye on the surface layer of the synthetic fiber from coming out onto the surface of the film, effectively preventing the dye from migrating and contaminating the coating layer that is subsequently processed. .
That is, by performing microwave heating according to the present invention, hydrogen abstraction reactions due to high energy state are likely to occur, crosslinking of the condensation product is promoted, and the densification of the resulting melamine film is increased. This seems to be the reason for the dramatic improvement in fastness. In the present invention, any well-known method can be used for applying the compound of formula [] and coating after the condensation treatment. That is, it is possible to use either wet or dry coating methods, any resin formulation such as urethane resin or acrylic resin, or any coating means such as a knife coater, pipe coater, reverse coater, kiss roll, etc. Furthermore, the migration stain prevention effect imparted by the present invention does not expire due to home washing, dry cleaning, etc., and the effect is semi-permanent. In addition, the texture of the fabric is hardly hardened, which is seen in conventional resin processing, and the fabric has good quality. The present invention will be further explained below with reference to Examples. Example 1 Polyester Pondy fabric (basis weight 220g/m 2 )
After descaling and scouring in a conventional manner, it is dried and heat treated at 180℃ for 30 seconds. Next, the specified dye, auxiliary agent, acetic acid 0.3
%, dyed at 130°C for 60 minutes at a bath ratio of 1:40, and after reduction washing, neutralization, washing with water, and drying. Next, it was immersed in a treatment solution with the following formulation, and after the squeezing rate was reduced to 60%, it was treated in a microwave irradiation chamber filled with saturated steam at 100℃ for 10 minutes at an output of 5kW, and then soaped with hot water for 5 minutes. , at 180℃
Dry heat set for 30 seconds. Resin formulation Sumitex Resin M-3 (manufactured by Sumitomo Chemical) 5 parts Sumitex Accellerator EPX (manufactured by Sumitomo Chemical)
Add 0.5 parts water to make total volume 100 parts. Using the dyed fabric as a base fabric, polyurethane transparent laminate coating was applied, and a polyurethane layer was applied to a thickness of 20 μm. Waxbon 7367 (Dainippon Ink KK) as a laminating resin
It was used. The resulting sample was examined for migration contamination using the following procedure. Attach a polyester taffeta (bleached) urethane transparent laminate with the urethane side aligned with the urethane side of the sample, sandwich it between two glass plates for a sweat tester, and apply a load of 4.5 kg. Place in a dryer at 80±2℃ and leave for 48 hours. Take out the composite specimen and allow it to cool to room temperature. The contamination visible on the attached cloth after the test was graded using a contamination gray scale. Furthermore, the color difference between the untreated sample and the treated sample was evaluated. These results are shown in Table 1. As is clear from Table 1, the treated fabric according to the present invention exhibited a remarkable effect of preventing migration staining, and had good quality without hardening in the hand. In addition, color difference (ΔE) is the color difference between untreated cloth and treated cloth using Shimadzu spectrophotometer Color Seven (C light source, 1976,
It was determined by measurement using La*b* method).
【表】
実施例 2
ポリエステルデシン織物(目付130g/m2)を
常法で糊抜き精練後、乾燥し、180℃で30秒間熱
処理する。次いで所定の染料、助剤、酢酸0.3%
を用い、浴比1:40において、130℃で60分染色
し、還元洗浄後、中和、水洗、乾燥する。つづい
て下記処方の処理液中に浸漬し、絞り率55%に絞
つた後、100℃の飽和水蒸気を充填したマイクロ
ウエーブ照射室内において、出力5kWで10分間
処理後、熱水で5分間ソーピングし、180℃で30
秒間乾熱セツトした。
また、比較のため、マイクロウエーブ照射を行
うことなく、上記の条件下に蒸熱処理のみを行つ
た試料をも作成した。
樹脂処方
Sumitex Resin M−3(住友化学工業製) 5部
Sumitex Accellerator EPX(住友化学工業製)
0.5部
水を加えて全量を100部とする。
該処理布を基布として実施例1と同様のコーテ
イング加工を行ない、試料を得た。
これらの試料の移行汚染度、および未処理品と
本発明品との色差を実施例1に順じて調べて表2
の結果を得た。
表2より明らかなように、マイクロウエーブ照
射による表面皮膜の緻密化によつて、処理布は、
未加工布および通常の蒸熱処理布に比較して、著
しい移行汚染防止効果を示すことがわかる。ま
た、処理布は、風合硬化もなく、良好な品位を有
していた。[Table] Example 2 A polyester deshine fabric (fabric weight 130 g/m 2 ) was desized and scoured in a conventional manner, dried, and heat treated at 180° C. for 30 seconds. Next, the specified dye, auxiliary agent, and acetic acid 0.3%
dyeing at 130°C for 60 minutes at a bath ratio of 1:40, followed by reduction washing, neutralization, washing with water, and drying. Next, it was immersed in a treatment solution with the following formulation, and the squeezing rate was reduced to 55%. After that, it was treated for 10 minutes at an output of 5kW in a microwave irradiation chamber filled with saturated steam at 100℃, and then soaped with hot water for 5 minutes. , 30 at 180℃
Dry heat set for seconds. For comparison, a sample was also prepared which was subjected to only steaming treatment under the above conditions without performing microwave irradiation. Resin formulation Sumitex Resin M-3 (manufactured by Sumitomo Chemical) 5 parts Sumitex Accellerator EPX (manufactured by Sumitomo Chemical)
Add 0.5 parts water to make total volume 100 parts. Using the treated fabric as a base fabric, the same coating process as in Example 1 was performed to obtain a sample. The degree of migration contamination of these samples and the color difference between the untreated product and the product of the present invention were investigated according to Example 1 and are shown in Table 2.
The results were obtained. As is clear from Table 2, due to the densification of the surface film by microwave irradiation, the treated fabric
It can be seen that compared to the untreated fabric and the normal steam-treated fabric, it exhibits a significant migration stain prevention effect. In addition, the treated fabric had good quality without any hardening.
【表】【table】
Claims (1)
OH、−OCoH2o+1、−CH2OCoH2o+1、−CH2OH、−
CH2CH2OH、−CH2CH2CH2OH、−CONH2、−
CONHCH2OH又は【式】を表わ す。ここにnは整数を表わす。〕 で示される化合物を付与し、マイクロウエーブ加
熱により縮合処理した後、該布帛をコーテイング
処理することを特徴とする染色布帛のコーテイン
グ加工方法。[Claims] 1. The following general formula [] is applied to the dyed fabric: [In the above formula, R 1 to R 6 are each independently -H, -
OH, −OC o H 2o+1 , −CH 2 OC o H 2o+1 , −CH 2 OH, −
CH2CH2OH , -CH2CH2CH2OH , -CONH2 , -
CONHCH 2 OH or [Formula]. Here n represents an integer. ] A method for coating a dyed fabric, which comprises applying a compound represented by the formula below and subjecting the fabric to a condensation treatment by microwave heating, and then coating the fabric.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57187385A JPS5982469A (en) | 1982-10-27 | 1982-10-27 | Coating process of dyed fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57187385A JPS5982469A (en) | 1982-10-27 | 1982-10-27 | Coating process of dyed fabric |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5982469A JPS5982469A (en) | 1984-05-12 |
JPH028068B2 true JPH028068B2 (en) | 1990-02-22 |
Family
ID=16205084
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57187385A Granted JPS5982469A (en) | 1982-10-27 | 1982-10-27 | Coating process of dyed fabric |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5982469A (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61186583A (en) * | 1985-02-11 | 1986-08-20 | 株式会社クラレ | Sheet like structure and its production |
JPS6228484A (en) * | 1985-07-30 | 1987-02-06 | 小松精練株式会社 | Fastness enhancing method |
JPS636184A (en) * | 1986-06-27 | 1988-01-12 | 帝人株式会社 | Dyed processed fabric |
JPH02200873A (en) * | 1989-01-25 | 1990-08-09 | Kuraray Co Ltd | Production of fiber structure |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5095583A (en) * | 1974-01-07 | 1975-07-30 |
-
1982
- 1982-10-27 JP JP57187385A patent/JPS5982469A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5095583A (en) * | 1974-01-07 | 1975-07-30 |
Also Published As
Publication number | Publication date |
---|---|
JPS5982469A (en) | 1984-05-12 |
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