JPS6339713B2 - - Google Patents
Info
- Publication number
- JPS6339713B2 JPS6339713B2 JP56094925A JP9492581A JPS6339713B2 JP S6339713 B2 JPS6339713 B2 JP S6339713B2 JP 56094925 A JP56094925 A JP 56094925A JP 9492581 A JP9492581 A JP 9492581A JP S6339713 B2 JPS6339713 B2 JP S6339713B2
- Authority
- JP
- Japan
- Prior art keywords
- chloride
- water
- treated
- emulsion
- fabric
- 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
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- 229920003043 Cellulose fiber Polymers 0.000 claims description 18
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 239000000839 emulsion Substances 0.000 claims description 13
- 239000002736 nonionic surfactant Substances 0.000 claims description 12
- 239000000440 bentonite Substances 0.000 claims description 11
- 229910000278 bentonite Inorganic materials 0.000 claims description 11
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 11
- 239000000986 disperse dye Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 235000013311 vegetables Nutrition 0.000 claims description 9
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 8
- 238000004513 sizing Methods 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 6
- 238000004043 dyeing Methods 0.000 claims description 4
- 239000004744 fabric Substances 0.000 description 27
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 241000047703 Nonion Species 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000007385 chemical modification Methods 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 238000010023 transfer printing Methods 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 238000003672 processing method Methods 0.000 description 4
- 235000010413 sodium alginate Nutrition 0.000 description 4
- 239000000661 sodium alginate Substances 0.000 description 4
- 229940005550 sodium alginate Drugs 0.000 description 4
- HDECRAPHCDXMIJ-UHFFFAOYSA-N 2-methylbenzenesulfonyl chloride Chemical compound CC1=CC=CC=C1S(Cl)(=O)=O HDECRAPHCDXMIJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- -1 Carboxylic acid chlorides Chemical class 0.000 description 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 description 2
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- MHXFWEJMQVIWDH-UHFFFAOYSA-N 1-amino-4-hydroxy-2-phenoxyanthracene-9,10-dione Chemical compound C1=C(O)C=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C1OC1=CC=CC=C1 MHXFWEJMQVIWDH-UHFFFAOYSA-N 0.000 description 1
- JDTUPLBMGDDPJS-UHFFFAOYSA-N 2-methoxy-2-phenylethanol Chemical compound COC(CO)C1=CC=CC=C1 JDTUPLBMGDDPJS-UHFFFAOYSA-N 0.000 description 1
- GPZXFICWCMCQPF-UHFFFAOYSA-N 2-methylbenzoyl chloride Chemical compound CC1=CC=CC=C1C(Cl)=O GPZXFICWCMCQPF-UHFFFAOYSA-N 0.000 description 1
- DGMOBVGABMBZSB-UHFFFAOYSA-N 2-methylpropanoyl chloride Chemical compound CC(C)C(Cl)=O DGMOBVGABMBZSB-UHFFFAOYSA-N 0.000 description 1
- RKIDDEGICSMIJA-UHFFFAOYSA-N 4-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=C(Cl)C=C1 RKIDDEGICSMIJA-UHFFFAOYSA-N 0.000 description 1
- SKDHHIUENRGTHK-UHFFFAOYSA-N 4-nitrobenzoyl chloride Chemical compound [O-][N+](=O)C1=CC=C(C(Cl)=O)C=C1 SKDHHIUENRGTHK-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 241001474374 Blennius Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 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 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 description 1
- 238000007754 air knife coating Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- MXMOTZIXVICDSD-UHFFFAOYSA-N anisoyl chloride Chemical compound COC1=CC=C(C(Cl)=O)C=C1 MXMOTZIXVICDSD-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- DVECBJCOGJRVPX-UHFFFAOYSA-N butyryl chloride Chemical compound CCCC(Cl)=O DVECBJCOGJRVPX-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000010017 direct printing Methods 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- MJGFBOZCAJSGQW-UHFFFAOYSA-N mercury sodium Chemical compound [Na].[Hg] MJGFBOZCAJSGQW-UHFFFAOYSA-N 0.000 description 1
- 239000000983 mordant dye Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 238000007777 rotary screen coating Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
Landscapes
- Coloring (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
【発明の詳細な説明】
本発明はセルロース繊維含有構造物の染色性改
善のための改質処理加工法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a modification treatment method for improving the dyeability of structures containing cellulose fibers.
従来から分散染料等の本来セルロース繊維に染
着を有さない染料を用いてセルロース繊維を良好
に染色しようする試みが特公昭47−40593、特公
昭47−51734、特開昭50−12389、特開昭50−
38213、特開昭50−90788、特公昭50−29552等に
示される様に、主に繊維処理方法によるものとし
てなされたり、通常は分散染料に親和性のないセ
ルロース繊維を化学的に改質する特開昭50−
18778、特開昭51−99185等の方法が知られてい
る。しかしながら、これらの上記繊維処理方法に
よるものは比較的簡単な装置を使用する事により
可能であるが、染色性に於いて鮮明さに欠けるこ
とや染色堅牢度、特に湿潤堅牢度が良好でない。
一方セルロースを化学改質するところの従来より
知られている方法では上記薬剤自身の刺激性およ
び臭気などから作業性が悪く且つ非常に高価な設
置投資を必要とする。 Previously, attempts have been made to successfully dye cellulose fibers using dyes such as disperse dyes that do not naturally dye cellulose fibers, such as Japanese Patent Publications No. 47-40593, No. 47-51734, No. 50-12389, No. 1977-
38213, JP-A No. 50-90788, JP-B No. 50-29552, etc., it is mainly done by fiber processing methods, or chemically modifying cellulose fibers that usually have no affinity for disperse dyes. Japanese Patent Publication 1973-
18778, Japanese Patent Application Laid-Open No. 51-99185, and other methods are known. However, although these fiber processing methods described above are possible by using relatively simple equipment, the dyeing property lacks sharpness and the color fastness, especially the wet fastness, is not good.
On the other hand, conventionally known methods of chemically modifying cellulose have poor workability due to the irritation and odor of the chemicals themselves, and require very expensive installation investment.
これらの問題を解決する為に本発明者等は先に
セルロース繊維又はセルロース繊維含有構造物に
アルカリ剤およびP−トルエンスルホニルクロリ
ド等の酸塩化物を任意の順序で処理した後に、更
に蒸熱処理又は乾熱処理を施して化学改質を行い
その後分散染料、油溶性染料、媒染染料、塩基性
染料、建染め染料等にて直接又は転写捺染すると
いう染色方法を発明し特許を出願した。さらに
は、かかる酸塩化物を水中に乳化した状態にて処
理することにより、この発明をさらに簡略化する
ことができるという発明も出願した。 In order to solve these problems, the present inventors first treated cellulose fibers or cellulose fiber-containing structures with an alkaline agent and an acid chloride such as P-toluenesulfonyl chloride in any order, and then further steam-treated or He invented a dyeing method that involved chemical modification through dry heat treatment, followed by direct or transfer printing with disperse dyes, oil-soluble dyes, mordant dyes, basic dyes, vat dyes, etc., and applied for a patent. Furthermore, the present invention has also been filed for an invention in which the present invention can be further simplified by treating the acid chloride in an emulsified state in water.
本発明はこれら従来の発明をさらに効果的でか
つ簡略化すべく実生産性を加味して発明したもの
である。 The present invention has been developed to make these conventional inventions more effective and simple, taking into account actual productivity.
即ち、本発明は、セルロース繊維含有構造物を
アルカリ剤にて処理し、続いて少なくとも酸塩化
物、植物性天然糊剤、ベントナイト、非イオン界
面活性剤を含有する水中乳化液にてコーテイング
処理し、続いて乾熱処理を施すことにより該構造
物のセルロース繊維部を分散染料可染性に化学改
質することを特徴とする改質処理加工方法であ
る。発明者等はセルロース繊維含有構造物のセル
ロース繊維部を酸塩化物の水中乳化液を用いて分
散染料可染性に化学改質するに際し、植物性天然
糊剤に加えてベントナイトを併用することによ
り、そのベントナイトの特性である無機性および
不活性の為に反応阻害の極めて少ない効率のよい
化学改質をすることができ、かつ化学改質後の余
剰付着物の離脱性が極めて良好であり、しかも洗
浄液中のベントナイトはその沈降性のために一般
排水処理にも利用されている様に極めて処分が簡
単であることを発見した。即ち本発明によると、
セルロース繊維含有構造物をアルカリ剤で処理し
た後、ウエツトの状態で少なくとも酸塩化物、植
物性天然糊剤、ベントナイト、非イオン界面活性
剤より成る水中乳化液をコーテイング処理し、続
いて通常の繊維布帛の乾燥装置、例えばピンテン
ターオーブン等による極めて簡単な既存の装置に
て乾燥することにより、セルロース繊維含有構造
物中のセルロース繊維部を分散染料可染性に化学
改質でき、しかもその後の洗浄が、ソーピング、
湯洗程度の極めて簡単な洗浄工程にて、余剰付着
物の除去ができる。発明者等が先に出願した
CMC(カルボキシメチルセルロース)等の繊維素
誘導体のみを増粘剤として含有している酸塩化物
の水中乳化液を用いたコーテイング処理によるセ
ルロース繊維部の分散染料可染性を目的とした化
学改質方法に於て実生産上困難な問題とされてい
た化学改質後の糊剤をはじめとする余剰付着物の
除去が本発明によりいつきに解決された。 That is, in the present invention, a structure containing cellulose fibers is treated with an alkaline agent, and then coated with an emulsion in water containing at least an acid chloride, a vegetable natural sizing agent, bentonite, and a nonionic surfactant. This modification processing method is characterized in that the cellulose fiber portion of the structure is chemically modified to be dyeable with a disperse dye by subsequently performing a dry heat treatment. The inventors chemically modified the cellulose fiber part of a cellulose fiber-containing structure using an acid chloride-in-water emulsion to make it dyeable with disperse dyes, and by using bentonite in addition to a vegetable natural sizing agent. Due to the inorganic and inert characteristics of bentonite, efficient chemical modification can be carried out with extremely little reaction inhibition, and the ability to remove excess deposits after chemical modification is extremely good. Moreover, it was discovered that bentonite in the cleaning solution is extremely easy to dispose of, as it is also used in general wastewater treatment due to its sedimentation properties. That is, according to the present invention,
After the cellulose fiber-containing structure is treated with an alkaline agent, it is coated in a wet state with an emulsion in water consisting of at least an acid chloride, a vegetable natural sizing agent, bentonite, and a nonionic surfactant. By drying the fabric using an extremely simple existing fabric drying device such as a pin tenter oven, the cellulose fibers in the cellulose fiber-containing structure can be chemically modified to be dyeable with disperse dyes, and furthermore, they can be washed easily after washing. But soaping,
Excess deposits can be removed with an extremely simple cleaning process such as washing with hot water. The inventor filed the application first.
A chemical modification method for making cellulose fibers dyeable with disperse dyes by coating with an acid chloride-in-water emulsion containing only cellulose derivatives such as CMC (carboxymethyl cellulose) as a thickener. The present invention has finally solved the problem of removing excess deposits such as glue after chemical modification, which has been a difficult problem in actual production.
本発明に使用されるアルカリ剤としては、例え
ばリチウム、ナトリウム、カリウム、ベリリウ
ム、マグネシウム、カルシウム、バリウム、スト
ロンチウム等のアルカリ金属あるいはアルカリ土
類金属の水酸化物である。 Examples of the alkaline agent used in the present invention include hydroxides of alkali metals or alkaline earth metals such as lithium, sodium, potassium, beryllium, magnesium, calcium, barium, and strontium.
また本発明に使用される酸塩化物としては、例
えば塩化ベンゾイル、塩化パラクロルベンゾイ
ル、塩化トルオイル、塩化パラニトロベンゾイ
ル、塩化パラメトキシベンゾイル、塩化アセチ
ル、塩化プロピオニル、塩化ブチリル、塩化イソ
ブチリル、塩化アクリロイル、塩化オキサリル、
塩化スクシニル等のカルボン酸塩化物や、パラト
ルエンスルホニルクロリド、オルトトルエンスル
ホニルクロリド、ベンゼンスルホニルクロイド、
メタニトロベンゼンスルホニルクロイド、オルト
ニトロベンゼンスルホニルクロイド、パラニトロ
ベンゼンスルホニルクロイド、トルエン−3,
4,ジスルホニルクロイド等の一般式が下記の構
造を有するスルホン酸塩化物があげられる。 Examples of acid chlorides used in the present invention include benzoyl chloride, parachlorobenzoyl chloride, toluoyl chloride, paranitrobenzoyl chloride, paramethoxybenzoyl chloride, acetyl chloride, propionyl chloride, butyryl chloride, isobutyryl chloride, acryloyl chloride, oxalyl chloride,
Carboxylic acid chlorides such as succinyl chloride, para-toluenesulfonyl chloride, orthotoluenesulfonyl chloride, benzenesulfonyl chloride,
Meta-nitrobenzenesulfonyl cloide, ortho-nitrobenzenesulfonyl cloide, para-nitrobenzenesulfonyl cloide, toluene-3,
4. Sulfonic acid chlorides such as disulfonyl chloride have the general formula shown below.
(XはH、−CH3、−NO2、SO2Clを意味する)
またさらに本発明で使用される植物性天然糊剤
としては、小麦粉、米粉、米糖、トウモロコシ等
の澱粉類、トラガントガム、アラビヤガム等の天
然ゴム類およびフノリ、アルギン酸ソーダ等の海
藻類である。 (X means H, -CH 3 , -NO 2 , SO 2 Cl) Furthermore, the vegetable natural thickening agents used in the present invention include starches such as wheat flour, rice flour, rice sugar, and corn, and gum tragacanth. , natural rubbers such as gum arabic, and seaweeds such as funori and sodium alginate.
さらに、セルロース繊維含有構造物をアルカリ
剤処理した後少なくとも酸塩化物、植物性天然糊
剤、ベントナイト、非イオン界面活性剤より成る
水中乳化液をコーテイング処理する方法として
は、植物性天然糊剤、ベントナイトおよび非イオ
ン界面活性剤の添加量により粘度を調製すること
ができ、ロールコート方式、スプレーコート方
式、エアーナイフコート方式、フローコート方
式、グラビアコート方式、ロータリースクリーン
方式等が行なえる。 Further, as a method of treating a cellulose fiber-containing structure with an alkali agent and then coating it with an emulsion in water consisting of at least an acid chloride, a vegetable natural sizing agent, bentonite, and a nonionic surfactant, a vegetable natural sizing agent, The viscosity can be adjusted by adjusting the amounts of bentonite and nonionic surfactant, and a roll coating method, a spray coating method, an air knife coating method, a flow coating method, a gravure coating method, a rotary screen method, etc. can be used.
以下更に本発明を図面を用いて詳細に説明す
る。即ち第1図は本発明に使用する改質装置の概
略図を示すもので、セルロース繊維含有構造物で
ある原布1はアルカリ槽2を通つてアルカリ剤の
処理量が均一になるように絞りロール3にて絞り
次いでロータリースクリーン式コーテイング装置
4,5,7に導入され少なくとも酸塩化物、植物
性天然糊剤、ベントナイト、非イオン界面活性剤
を含有する水中乳化液を均一に処理される。即ち
4はロータリースクリーン版を示し、7はバツク
アツプロール、5はスキージーを示し、6はロー
タリースクリーン版中に供給された少なくとも酸
塩化物、植物性天然糊剤、ベントナイト、非イオ
ン界面活性剤を含有する水中乳化液を示し、スキ
ージー5とバツクアツプロール7との圧力により
ロータリースクリーン版4を通じて原布1上に処
理される。水中乳化液を処理された布帛は乾燥ド
ライヤー8に導かれ8を通過した時点で化学改質
を終了し、次いでソーピング液槽9、湯浴槽1
0、水浴槽11を順次通過した後乾燥ドライヤー
12にて十分乾燥され目的とする分散染料可染性
の化学改質布13が得られる。 The present invention will be further explained in detail below using the drawings. That is, FIG. 1 shows a schematic diagram of the reforming apparatus used in the present invention, in which raw fabric 1, which is a cellulose fiber-containing structure, is passed through an alkali tank 2 and squeezed so that the amount of alkaline agent treated is uniform. It is squeezed by a roll 3 and then introduced into rotary screen coating devices 4, 5, and 7, where it is uniformly treated with an emulsion in water containing at least an acid chloride, a vegetable natural sizing agent, bentonite, and a nonionic surfactant. That is, 4 indicates a rotary screen plate, 7 indicates a back-up roll, 5 indicates a squeegee, and 6 indicates at least an acid chloride, a vegetable natural sizing agent, bentonite, and a nonionic surfactant supplied in the rotary screen plate. The water-in-water emulsion contained therein is processed onto the raw fabric 1 through the rotary screen plate 4 by the pressure of the squeegee 5 and the back-up roll 7. The fabric treated with the water emulsion is led to a dryer 8, where chemical modification is completed when it passes through the dryer 8, and then to a soaping liquid tank 9 and a hot water bath 1.
0. After successively passing through a water bath 11, the fabric is sufficiently dried in a dryer 12 to obtain the desired chemically modified fabric 13 dyeable with disperse dyes.
以下、実施例にて更に詳細な説明とする。 A more detailed explanation will be given below in Examples.
実施例 1
(1) シルケツト加工済みのポリエステル/木綿=
65/35なる混紡ブロート布を10%水酸化ナトリ
ウム水溶液中に浸漬した後、絞り率90%になる
様絞りロールにて絞つた。次にこの繊維布帛を
下記する処方より成る水中乳化液を用いて、線
数40線/inchニツケル版厚150μ、開口率50%か
らなるロータリースクリーン版にて処理した。Example 1 (1) Mercerized polyester/cotton =
A 65/35 blended bloat cloth was immersed in a 10% aqueous sodium hydroxide solution, and then squeezed using a squeezing roll to achieve a squeezing rate of 90%. Next, this fiber fabric was treated with an emulsion in water having the following formulation using a rotary screen plate having a nickel plate thickness of 150 μm and an aperture ratio of 50% with a number of lines of 40 lines/inch.
乳化液
O−トルエンスルホニルク
ロリド 25重量部
トルエン 25 〃
水 50 〃
アルギン酸ソーダ 1 〃
ベンナイト 2 〃
ニツサンノニオンNS−
206(日本油脂社製非イオ
ン界面活性剤) 1.5 〃
ニツサンノニオンNS−
210(日本油脂社製非イオ
ン界面活性剤) 1.5 〃
ニツサンノニオンNS−
220(日本油脂社製非イオ
ン界面活性剤) 1.5 〃
次にこの処理布をピンテンターオーブンを用
いて80℃、90秒間乾熱処理した後、マルセル石
鹸によるソーピング、湯洗、水洗を行つた数十
分乾燥して改質布を得た。Emulsified liquid O-Toluenesulfonyl chloride 25 parts by weight Toluene 25 〃 Water 50 〃 Sodium alginate 1 〃 Bennite 2 〃 Nitsusan Nonion NS- 206 (Nonionic surfactant manufactured by NOF Corporation) 1.5 〃 Nitsusan Nonion NS- 210 (Japan Nitsusan Nonion NS-220 (Nonionic surfactant manufactured by Nihon Yushi Co., Ltd.) 1.5 Next, this treated cloth was dry heat treated at 80°C for 90 seconds using a pin tenter oven. Thereafter, the cloth was soaped with Marcel soap, washed with hot water, washed with water, and dried for several minutes to obtain a modified cloth.
(2) 次に60g/m2の片面スターチコート紙に下記
組成のインキによりグラビア印刷して転写紙を
得た。(2) Next, gravure printing was performed on 60 g/m 2 single-sided starch-coated paper using ink having the composition shown below to obtain a transfer paper.
<インキ>
スミカロンレツドE−FBL原末
(住友化学社製) 10重量部
エチルセルロースN−7
(ハーキユリーズ社製) 9 〃
界面活性剤 1 〃
イソプロピルアルコール 40 〃
エチルアルコール 40 〃
(3) (1)なる改質布に(2)なる転写紙を重ね合わせ、
温度195℃、圧300g/cm2、時間40秒の条件にて
加熱、加圧して転写捺染を行つたところ、ポリ
エステル繊維部、木綿部が同一の濃度ある赤色
の捺染布が得られた。 <Ink> Sumikaron Red E-FBL bulk powder (manufactured by Sumitomo Chemical Co., Ltd.) 10 parts by weight Ethylcellulose N-7 (manufactured by Hercules Co., Ltd.) 9 〃 Surfactant 1 〃 Isopropyl alcohol 40 〃 Ethyl alcohol 40 〃 (3) (1) Naru Kai Layer the transfer paper (2) on the pawn cloth,
When transfer printing was carried out by heating and applying pressure at a temperature of 195° C., a pressure of 300 g/cm 2 , and a time of 40 seconds, a red printed cloth with the same density in the polyester fiber portion and the cotton portion was obtained.
実施例 2
(1) シルケツト加圧済みのポリエステル/木綿=
65/35よりなる混紡ブロード布を10%水銀化ナ
トリウム水溶液に侵漬し、絞り率90%になる様
絞りロールにて絞つた。次にこの繊維布帛を下
記する処方より成る乳化液を用いて実施例1の
(1)に記載のロータリースクリーン版にて処理し
た。Example 2 (1) Mercerized polyester/cotton =
A blended broad cloth made of 65/35 was immersed in a 10% sodium mercury aqueous solution and squeezed using a squeezing roll to achieve a squeezing rate of 90%. Next, this fiber fabric was processed according to Example 1 using an emulsion having the following formulation.
It was processed using the rotary screen plate described in (1).
乳化液
O−トルエンスルホニルク
ロリド 10重量部
P−トルエンスルホニルク
ロリド 15 〃
トルエン 25 〃
水 50 〃
アルギン酸ソーダ 1 〃
ベントナイト 2 〃
ニツサンノニオンNS−
206(日本油脂社製非イオ
ン界面活性剤) 1.5 〃
ニツサンノニオンNS−
210(日本油脂社製非イオ
ン界面活性剤) 1.5 〃
ニツサンノニオンNS−
220(日本油脂社製非イオ
ン界面活性剤) 1.5 〃
次にこの処理布をピンテンターオーブンを用
いて100℃、30秒間乾熱処理した後、マルセル
石鹸によるソーピング、湯洗、水洗を行つた
後、十分乾燥して改質布を得た。Emulsified liquid O-toluenesulfonyl chloride 10 parts by weight P-toluenesulfonyl chloride 15 〃 Toluene 25 〃 Water 50 〃 Sodium alginate 1 〃 Bentonite 2 〃 Nitsusan Nonion NS- 206 (nonionic surfactant manufactured by NOF Corporation) 1.5 〃 Nitsu Sunnonion NS- 210 (nonionic surfactant manufactured by NOF Corporation) 1.5 〃 Nitsusan Nonion NS- 220 (nonionic surfactant manufactured by NOF Corporation) 1.5 〃 Next, this treated cloth was heated to 100% using a pin tenter oven. After dry heat treatment at ℃ for 30 seconds, soaping with Marcel soap, washing with hot water, washing with water, and thorough drying to obtain a modified fabric.
(2) 次に(1)によつて得られた改質布に凸版印刷社
製の乾式転写捺染紙を用いて195℃、35秒間150
g/cm2の圧力下で転写捺染を行つたところ実し
いプリント布を得た。(2) Next, the modified fabric obtained in (1) was heated at 195℃ for 35 seconds using a dry transfer printing paper manufactured by Toppan Printing Co., Ltd.
When transfer printing was carried out under a pressure of g/cm 2 , a realistic printed fabric was obtained.
実施例 3
(1) シルケツト加圧済みのポリエステル/木綿=
65/35より成る混紡ブロード布を10%NaOH
水溶液に浸漬し、絞り率90%になる様絞りロー
ルにて絞つた。次にこの繊維布帛を下記処方よ
り成る乳化液を用いて実施例1の(1)に記載のロ
ータリースクリーン版にて処理した。Example 3 (1) Mercerized polyester/cotton =
65/35 blended broadcloth with 10% NaOH
It was immersed in an aqueous solution and squeezed with a squeezing roll to achieve a squeezing rate of 90%. Next, this fiber fabric was treated with the rotary screen plate described in Example 1 (1) using an emulsion having the following formulation.
塩化ベンゾイル 15重量部
トルエン 15 〃
水 50 〃
アルギン酸ソーダ 1 〃
乳化液
ベンナイト 2 〃
ニツサンノニオンNS−206 1.5 〃
ニツサンノニオンNS−210 1.5 〃
ニツサンノニオンNS−220 1.5 〃
次にこの処理布をピンテンターオーブンにて
100℃、30秒間乾熱処理した後、マルセン石鹸
によるソーピング、湯洗、水洗を行なつた後、
十分乾燥して改質布を得た。Benzoyl chloride 15 parts by weight Toluene 15 Water 50 Sodium alginate 1 Emulsified benite 2 Nitsusan Nonion NS-206 1.5 Nitsusan Nonion NS-210 1.5 Nitsusan Nonion NS-220 1.5 Next, use this treated cloth In pin tenter oven
After dry heat treatment at 100℃ for 30 seconds, soaping with Marsen soap, washing with hot water, and then washing with water,
After sufficient drying, a modified cloth was obtained.
(2) 次に(1)によつて得られた改質布に凸版印刷社
製の乾式転写捺染紙を用いて、195℃、35秒間、
150g/cm2の圧力下で転写捺染を行つたところ
美しいプリント布を得た。(2) Next, using dry transfer printing paper manufactured by Toppan Printing Co., Ltd., the modified fabric obtained in (1) was heated at 195°C for 35 seconds.
Transfer printing was carried out under a pressure of 150 g/cm 2 and a beautiful printed cloth was obtained.
図面は本発明の1実施例を示すもので、第1図
は本発明の改質処理加工法に使用する装置の概略
図を示す。
1……原布、2……アルカリ槽、3……絞りロ
ール、4……ロータリースクリーン版、5……ス
キージー、6……乳化液、7……バツクアツプロ
ール、8……乾燥ドライヤー、9……ソーピング
浴槽、10……湯浴槽、11……水浴槽、12…
…乾燥ドライヤー、13……改質布。
The drawings show one embodiment of the present invention, and FIG. 1 shows a schematic diagram of an apparatus used in the modification processing method of the present invention. 1... Raw fabric, 2... Alkali tank, 3... Squeezing roll, 4... Rotary screen plate, 5... Squeegee, 6... Emulsion, 7... Back-up roll, 8... Dryer, 9 ...Soaping bathtub, 10...Hot bathtub, 11...Water bathtub, 12...
...Drying dryer, 13...Modified cloth.
Claims (1)
処理し続いて少なくとも酸塩化物、植物性天然糊
剤、ベントナイト、非イオン界面活性剤を含有す
る水中乳化液にてコーテイング処理し、続いて乾
熱処理を施すことにより該構造物のセルロース繊
維部を分散染料可染性に化学改質した後、分散染
料で染色することを特徴とする染色方法。1. A cellulose fiber-containing structure is treated with an alkaline agent, then coated with an emulsion in water containing at least an acid chloride, a vegetable natural sizing agent, bentonite, and a nonionic surfactant, followed by a dry heat treatment. A dyeing method characterized by chemically modifying the cellulose fiber portion of the structure to make it dyeable with a disperse dye, and then dyeing it with a disperse dye.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56094925A JPS57210086A (en) | 1981-06-19 | 1981-06-19 | Treatment for modifying cellulose fiber containing structure |
DE8181109596T DE3171259D1 (en) | 1981-06-15 | 1981-11-10 | Method of modifying the dye affinity of cellulose fiber-containing structure |
EP81109596A EP0067904B1 (en) | 1981-06-15 | 1981-11-10 | Method of modifying the dye affinity of cellulose fiber-containing structure |
AU77384/81A AU545521B2 (en) | 1981-06-15 | 1981-11-11 | Modifying dye affinity in cellulose fibres |
US06/320,763 US4392265A (en) | 1981-06-15 | 1981-11-12 | Method of modifying the dye affinity of cellulose fiber-containing structure with benzene sulfonyl chloride |
CA000390419A CA1173601A (en) | 1981-06-15 | 1981-11-19 | Method of modifying the dye affinity of cellulose fiber-containing structure |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56094925A JPS57210086A (en) | 1981-06-19 | 1981-06-19 | Treatment for modifying cellulose fiber containing structure |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57210086A JPS57210086A (en) | 1982-12-23 |
JPS6339713B2 true JPS6339713B2 (en) | 1988-08-08 |
Family
ID=14123540
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56094925A Granted JPS57210086A (en) | 1981-06-15 | 1981-06-19 | Treatment for modifying cellulose fiber containing structure |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57210086A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3643864A1 (en) * | 1986-12-22 | 1988-06-30 | Cassella Ag | LIQUID SETTINGS OF DISPERSION DYES FOR COLORING TEXTILE MATERIALS |
JP4744224B2 (en) * | 2005-08-03 | 2011-08-10 | セーレン株式会社 | Pretreatment method for preventing thermal embrittlement of cellulose-containing fabric |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57210079A (en) * | 1981-06-15 | 1982-12-23 | Toppan Printing Co Ltd | Dyeing method |
-
1981
- 1981-06-19 JP JP56094925A patent/JPS57210086A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57210079A (en) * | 1981-06-15 | 1982-12-23 | Toppan Printing Co Ltd | Dyeing method |
Also Published As
Publication number | Publication date |
---|---|
JPS57210086A (en) | 1982-12-23 |
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