JPS6158596B2 - - Google Patents
Info
- Publication number
- JPS6158596B2 JPS6158596B2 JP54156869A JP15686979A JPS6158596B2 JP S6158596 B2 JPS6158596 B2 JP S6158596B2 JP 54156869 A JP54156869 A JP 54156869A JP 15686979 A JP15686979 A JP 15686979A JP S6158596 B2 JPS6158596 B2 JP S6158596B2
- Authority
- JP
- Japan
- Prior art keywords
- fabric
- printed
- bath
- fibers
- dye
- 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
- 239000004744 fabric Substances 0.000 claims description 34
- 239000007844 bleaching agent Substances 0.000 claims description 31
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 23
- 239000000460 chlorine Substances 0.000 claims description 23
- 229910052801 chlorine Inorganic materials 0.000 claims description 23
- 238000011282 treatment Methods 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 17
- 239000000835 fiber Substances 0.000 claims description 15
- 239000004753 textile Substances 0.000 claims description 9
- 238000004043 dyeing Methods 0.000 claims description 5
- 239000000975 dye Substances 0.000 description 17
- 238000011109 contamination Methods 0.000 description 16
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 13
- 239000000463 material Substances 0.000 description 13
- 239000000986 disperse dye Substances 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000004952 Polyamide Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920002647 polyamide Polymers 0.000 description 5
- 238000010186 staining Methods 0.000 description 5
- 229920002994 synthetic fiber Polymers 0.000 description 5
- 239000000980 acid dye Substances 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000012209 synthetic fiber Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- 239000005708 Sodium hypochlorite Substances 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- -1 cotton Chemical compound 0.000 description 3
- 238000006298 dechlorination reaction Methods 0.000 description 3
- 239000003292 glue Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 235000017550 sodium carbonate Nutrition 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 3
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 2
- 239000000985 reactive dye Substances 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- OXLITIGRBOEDEZ-UHFFFAOYSA-N 1,5-diamino-4,8-dihydroxy-2-(4-hydroxyphenyl)anthracene-9,10-dione Chemical compound C=1C(O)=C2C(=O)C=3C(N)=CC=C(O)C=3C(=O)C2=C(N)C=1C1=CC=C(O)C=C1 OXLITIGRBOEDEZ-UHFFFAOYSA-N 0.000 description 1
- RTLULCVBFCRQKI-UHFFFAOYSA-N 1-amino-4-[3-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-sulfoanilino]-9,10-dioxoanthracene-2-sulfonic acid Chemical compound C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C(S(O)(=O)=O)C=C1NC(C=1)=CC=C(S(O)(=O)=O)C=1NC1=NC(Cl)=NC(Cl)=N1 RTLULCVBFCRQKI-UHFFFAOYSA-N 0.000 description 1
- 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 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- ZKQDCIXGCQPQNV-UHFFFAOYSA-N Calcium hypochlorite Chemical compound [Ca+2].Cl[O-].Cl[O-] ZKQDCIXGCQPQNV-UHFFFAOYSA-N 0.000 description 1
- 208000028553 Relative Energy Deficiency in Sport Diseases 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 229920002472 Starch Polymers 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
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- HRKQOINLCJTGBK-UHFFFAOYSA-N dihydroxidosulfur Chemical class OSO HRKQOINLCJTGBK-UHFFFAOYSA-N 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000010447 natron Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229920006306 polyurethane fiber Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
- 239000004758 synthetic textile Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Coloring (AREA)
Description
本発明は、染色した繊維製品の品位と品質が著
るしく向上する処理法に関するものである。さら
に詳しくは、捺染した、又は異種繊維の混用布帛
を染色して得た繊維製品のソーピング時に汚染を
防止し、併せて、染色堅ろう度と鮮明性を向上さ
せる処理法に関するものである。
天然繊維、再生繊維、半合成繊維および合成繊
維などの単一の繊維からなる布帛の捺染物やこれ
らの繊維の組合せによる混紡、交織、混繊などの
混用品に、それぞれの繊維に可染性の1種または
2種以上の染料を使用して、捺染または染色した
繊維製品、特にポリエステル側を分散染料で染着
したものについては、ソーピング時、分散染料が
交織または混紡などの組合わせる相手素材を汚染
したり、または、捺染物の白場部分を汚染する問
題があるため、品位が著しく悪かつた。
ポリエステル用分散染料を用いて染色したポリ
エステル混用品は染色堅牢度の向上のため、還元
洗浄するのが、つまり、ハイドロサルフアイト、
カセイソーダ及び界面活性剤を含む処理浴で80℃
前後で処理するのが普通である。しかしながら、
ポリエステル用分散染料の他素材への汚染が50℃
近くから起りはじめるため、処理温度を50℃以下
にせざるを得ないことが少なくない。とくにポリ
エステル/ポリアミド混用品ではこのような事が
多い。しかし、かかる場合には、当然、染色堅牢
度、特に耐洗濯、耐摩擦堅牢度が不良となり、さ
らに鮮明性にも劣るのである。
本発明者らは、先に、該布帛の汚染を防止する
ため、塩素系漂白剤を含有したアルカリ性ソーピ
ング浴で処理することを提案している。しかしな
がら、この方法においても、汚染は改善できる
が、効果は完全なものではなかつた。つまり、塩
素系漂白剤による酸化だけでは染料の脱色が不完
全で、淡く着色してソーピング浴中に残り、これ
が布帛に再吸着されるため、白場汚染を防止する
ことには限界があつた。また、還元剤を含有した
酸性浴で処理すれば、白場汚染の防止には効果的
であるが、染着している相手素材を脱色させる欠
点があつた。
本発明者らは、染色物が脱色されることなく、
白場汚染のないソーピング方法を鋭意研究の結
果、塩素系漂白剤と還元漂白剤で処理することに
よつて、全ての繊維の染色または、捺染製品の汚
染が防止できる画期的な方法を見い出すに到つ
た。すなわち、本発明は、「布帛を捺染した後、
又は、異種繊維の混用布帛を染色した後、塩素系
漂白剤を含有したアルカリ性ソーピング浴で処理
し、次いで、還元漂白剤で処理することを特徴と
する繊維製品の後処理法」である。
もともと、酸化剤である塩素系漂白剤と還元漂
白剤を併用すれば、効果が相殺される懸念があつ
た。しかしながら、本発明者らの研究によれば、
まず、塩素系漂白剤で処理し、昇温後、還元漂白
剤を添加すれば、両者の作用が失われないことが
明確になつた。すなわち、酸化剤である塩素漂白
剤は、低温で活性があるので先に添加しておき、
還元漂白剤の活性化が起る温度に昇温した後、還
元剤を添加すると、塩素系漂白剤で分解した分解
物である着色物が、さらに分解され、浴中で無色
になることが明らかになつた。この理由により、
ソーピングによる汚染がほとんどない捺染物や異
種繊維の混用布帛の染色物が得られるに到つた。
ここで、本発明をさらに詳しく説明する。本発
明で云うソーピング浴とは、染色または、捺染品
の汚染の防止、染色堅牢度の向上や鮮明性の向上
などを目的としたものであつて、その組成は、公
知である水酸化ナトリウム、炭酸ナトリウム、ア
ンモニア水や硅酸ナトリウムなどのアルカリ性物
質と石鹸や合成洗剤などの界面活性剤から成るも
のである。この浴に添加する塩素系漂白剤として
は、アルカリ性で活性なサラシ粉、次亜塩素酸ナ
トリウムなどが挙げられる。
塩素系漂白剤は、ソーピング浴に遊離した染料
を選択的に分解するものと思われる。したがつ
て、一たん汚染された染色物に対しては効果がな
い。一般に、ソーピング浴においては、比較的低
温で染料の遊離がはじまり、それより高温で汚染
がはじまるが、塩素系漂白剤は、汚染のはじまる
温度よりも低温で活性があるため、遊離した染料
が白場や、本来目的としない繊維を汚染する機会
を極めて少なくする。一方、先に、還元漂白剤で
処理し、次いで、塩素系漂白剤で処理しても、全
く、白場汚染を防止することはできない。塩素系
漂白剤で処理し、次いで、還元漂白剤で処理する
ことが必須である。
塩素系漂白剤の使用量は、多く使用することは
不経済であるので有効成分の量により、また、使
用染料や染色濃度などにより、増減させることが
必要である。例えば、ポリエステル/綿混を分散
染料/反応性染料で染色したものには、有効塩素
約11%の次亜塩素酸ナトリウム溶液をソーピング
浴の重量に対し、0.2%から1.0%でよいが、捺染
物に対しては、0.5%から2.0%が好ましい。ま
た、ポリアミド/ポリウレタンを酸性染料で捺染
したものには、0.1%から0.5%で良い。有効成分
が、約30%のサラシ粉を使用する場合には、先に
述べた次亜塩素酸ナトリウムの使用量の50%から
30%程度で十分である。
汚染物または、異種繊維の混用布帛に染液を付
着、乾燥した後、発色固着により得た染色物に対
しては、十分、冷水で水洗または、低温で、アル
カリ性ソーピング浴で十分、糊落しを行つた後、
塩素系漂白剤を含有したアルカリ性ソーピング浴
で、低温から処理し、徐々に昇温するのが望まし
い。
還元漂白剤には、ハイドロサルフアイトと呼ば
れるヒドロ亜硫酸ナトリウム、亜硫酸ガス、酸性
亜硫酸ナトリウム、スルホキシレート・ホルムア
ルデヒド類などがあるが、アルカリ性で安定で、
しかも、染色物を脱色させず、取扱いが容易なハ
イドロサルフアイトが最も望ましい。使用量とし
ては、多く使用すると不経済であるので、有効成
分や染色濃度、塩素系漂白剤の使用量などによつ
て、ソーピング浴の重量に対し、0.05%から5%
の範囲で増減することが望ましい。
還元漂白剤は、初めから、塩素系漂白剤の浴中
に添加するよりも、ハイドロサルフアイトの活性
化が始まる温度以上で添加した方がより効果的で
ある。連続して処理する場合には、水洗槽、アル
カリ性塩素漂白槽、次いで、アルカリ性ハイドロ
サルフアイト槽を設けて処理することも可能であ
る。
ハイドロサルフアイトは、アルカリ性浴中では
50℃近くから活性化が始まるため、この温度以上
で添加することが望ましい。しかしながら、白場
汚染の防止効果は、使用染料により異なり、50℃
でハイドロサルフアイトを添加して、分散染料を
使用した捺染物や染色物には、80℃以上、カチオ
ン染料や酸性染料を使用したものには60℃以上に
添加して、昇温しても、汚染が発生しないタイプ
と、50℃で一度、汚染が防止できても、昇温によ
り、再汚染するタイプがある。後者の染料タイプ
には、ハイドロサルフアイトの添加時期を遅ら
せ、塩素系漂白剤を含有したアルカリ性ソーピン
グ浴で60℃以上で処理した後、その浴の中にハイ
ドロサルフアイトの所定量を添加し、汚染がなく
なるまで処理することが望ましい。これにより、
染料の分解物である着色物をハイドロサルフアイ
トでさらに分解するため、汚染が防止できるもの
である。
このような処理において、残留塩素により、脆
化したり、黄化する繊維製品、例えば、綿、羊
毛、ナトロン、ポリウレタンなどには、過酸化水
素、チオ硫酸ナトリウムや酸性亜硫酸ナトリウム
などで処理することが望ましい。
本発明は、天然繊維、再生繊維、半合成繊維お
よび合成繊維または、これらの繊維を含む織物、
編物、不織布、カーペツトなどの繊維製品と、こ
れらの繊維製品に染着可能な染料種属に適用でき
るものである。とくに、分散染料を用いる場合や
ポリアミドとポリウレタン繊維の混用布帛の捺染
品において、汚染が起こりやすいので有用であ
る。
以下、実施例にて、本発明を詳細に説明する。
実施例 1
ポリエステル/綿(65/35)混織物を下記処法
の色糊を用いて、オートスクリーン捺染機にて水
玉柄を印捺した。
DIANIX BLUE BG―FS 50g
(三菱化成製、分酸染料)
PROCION BLUE H―5R 20g
(I.C.I.製、反応性染料)
尿 素 50g
ソーダ灰 20g
MSパウダー 30g
(明成化学製、還元防止剤)
アルギン酸ナトリウムNSPM 500g
(固型分10%、鴨川化成製、糊剤)
温 湯 330g
計 1000g
この印捺布を100℃で2分乾燥した後、190℃で
60秒間処理して、染料固着を行なつた。この捺染
布を水洗し、浴比1:40にて下記A、B、C処法
のソーピング浴で30℃から昇温し、80℃で20分間
処理した。
The present invention relates to a treatment method that significantly improves the quality and quality of dyed textile products. More specifically, the present invention relates to a treatment method that prevents contamination during soaping of textile products obtained by printing or dyeing fabrics made of a mixture of different fibers, and also improves color fastness and brightness. Printed fabrics made of single fibers such as natural fibers, recycled fibers, semi-synthetic fibers, and synthetic fibers, as well as mixed products such as blends, interwovens, and mixed fibers made of combinations of these fibers, are dyeable to each fiber. For textile products printed or dyed using one or more of the following dyes, especially those dyed with disperse dyes on the polyester side, when soaping, the disperse dyes may be mixed with the mating material such as interweaving or blending. The quality of the printed material was extremely poor due to the problem of contaminating the printed material or the white areas of the printed material. Polyester blend products dyed using disperse dyes for polyester should be reduced and washed to improve color fastness, i.e. hydrosulfite,
80℃ in a treatment bath containing caustic soda and surfactant
It is normal to process before and after. however,
Disperse dye for polyester contamination of other materials at 50℃
Because it begins to occur nearby, it is often necessary to lower the processing temperature below 50°C. This is especially common with polyester/polyamide mixed products. However, in such a case, the color fastness, particularly the washing and abrasion fastnesses, will naturally be poor, and the clarity will also be poor. The present inventors have previously proposed treating the fabric with an alkaline soaping bath containing a chlorine bleach in order to prevent contamination of the fabric. However, even with this method, although contamination could be improved, the effect was not complete. In other words, oxidation with chlorine bleach alone does not completely decolorize the dye, leaving a faint color in the soaping bath, which is re-absorbed by the fabric, so there is a limit to how well it can prevent white spot contamination. . Furthermore, treatment with an acidic bath containing a reducing agent is effective in preventing white spot staining, but has the disadvantage of decolorizing the dyed material. The present inventors have discovered that the dyed material is not bleached,
As a result of intensive research on soaping methods that do not cause surface contamination, we have discovered an innovative method that can prevent contamination of all textile dyeing and printed products by treating them with chlorine bleach and reducing bleach. I reached it. In other words, the present invention provides, ``After printing the fabric,
Alternatively, it is a post-treatment method for textile products, which comprises dyeing a mixed fabric of different types of fibers, treating it with an alkaline soaping bath containing a chlorine bleach, and then treating it with a reducing bleach. Originally, there was a concern that if chlorine bleach, which is an oxidizing agent, and reducing bleach were used together, the effects would cancel each other out. However, according to the research of the present inventors,
First, it became clear that if the material is treated with a chlorine bleach and then a reducing bleach is added after the temperature is raised, the effects of both will not be lost. In other words, chlorine bleach, which is an oxidizing agent, is active at low temperatures, so add it first.
It is clear that when a reducing agent is added after the temperature is raised to a temperature at which the reducing bleach becomes activated, the colored substances, which are decomposition products of the chlorine bleach, are further decomposed and become colorless in the bath. It became. For this reason,
It has now been possible to obtain printed fabrics and dyed fabrics containing mixed fibers with almost no staining due to soaping. The present invention will now be described in more detail. The soaping bath referred to in the present invention is intended for the purpose of preventing staining of dyed or printed products, improving color fastness, and improving brightness, and the composition thereof is known sodium hydroxide, It consists of alkaline substances such as sodium carbonate, aqueous ammonia, and sodium silicate, and surfactants such as soap and synthetic detergents. Examples of the chlorine bleach that can be added to this bath include alkaline and active bleaching powder, sodium hypochlorite, and the like. Chlorine bleach appears to selectively destroy dyes released into the soaping bath. Therefore, it is not effective against dyed materials once they have been contaminated. In general, in soaping baths, dyes begin to be liberated at relatively low temperatures, and contamination begins at higher temperatures, but chlorine bleach is active at a lower temperature than the temperature at which contamination begins, so the liberated dyes become white. To minimize the chance of contaminating the fabric or fibers that are not originally intended. On the other hand, even if the surface is first treated with a reducing bleach and then treated with a chlorine bleach, it is not possible to prevent white spot contamination at all. It is essential to treat with chlorine bleach and then with reducing bleach. Since it is uneconomical to use a large amount of chlorine bleach, it is necessary to increase or decrease the amount of chlorine bleach depending on the amount of active ingredients, the dye used, the dyeing concentration, etc. For example, for polyester/cotton blends dyed with disperse dyes/reactive dyes, a sodium hypochlorite solution containing approximately 11% available chlorine may be added at 0.2% to 1.0% by weight of the soaping bath; For substances, 0.5% to 2.0% is preferred. In addition, for polyamide/polyurethane printed with acid dyes, 0.1% to 0.5% is sufficient. When using salashi powder with an active ingredient of about 30%, the amount of sodium hypochlorite used is 50% of the amount mentioned above.
Approximately 30% is sufficient. For dyed products obtained by color development and fixation after applying the dye solution to a contaminated item or a fabric mixed with different types of fibers and drying, wash thoroughly with cold water or thoroughly remove the size using an alkaline soap bath at a low temperature. After going,
It is preferable to start at a low temperature and gradually increase the temperature using an alkaline soaping bath containing chlorine bleach. Reductive bleaches include sodium hydrosulfite called hydrosulfite, sulfur dioxide gas, acidic sodium sulfite, and sulfoxylates/formaldehydes, which are alkaline and stable.
Furthermore, hydrosulfite is most desirable because it does not bleach the dyed material and is easy to handle. The amount used is 0.05% to 5% of the weight of the soaping bath, depending on the active ingredients, dye concentration, amount of chlorine bleach used, etc., as it is uneconomical to use too much.
It is desirable to increase or decrease within the range of . It is more effective to add the reducing bleach at a temperature higher than the temperature at which hydrosulfite activation begins, rather than adding it to the chlorine bleach bath from the beginning. In the case of continuous treatment, it is also possible to provide a washing tank, an alkaline chlorine bleaching tank, and then an alkaline hydrosulfite tank. In an alkaline bath, hydrosulfite
Since activation begins near 50°C, it is desirable to add at a temperature above this temperature. However, the effectiveness of preventing white field contamination varies depending on the dye used.
Hydrosulfite is added at temperatures above 80℃ for printed and dyed fabrics using disperse dyes, and above 60℃ for fabrics using cationic dyes and acid dyes, even at elevated temperatures. There are two types: one type that does not cause contamination, and the other type that, even if contamination can be prevented once at 50°C, re-contamination occurs when the temperature rises. For the latter dye type, the timing of addition of hydrosulfite is delayed, and after treatment in an alkaline soaping bath containing chlorine bleach at 60°C or higher, a predetermined amount of hydrosulfite is added to the bath. It is desirable to treat until there is no contamination. This results in
Since colored substances, which are decomposition products of dyes, are further decomposed with hydrosulfite, pollution can be prevented. In such treatments, textile products that become brittle or yellow due to residual chlorine, such as cotton, wool, natron, and polyurethane, can be treated with hydrogen peroxide, sodium thiosulfate, or acidic sodium sulfite. desirable. The present invention relates to natural fibers, regenerated fibers, semi-synthetic fibers, synthetic fibers, or fabrics containing these fibers,
It can be applied to textile products such as knitted fabrics, nonwoven fabrics, and carpets, as well as dye types that can be dyed to these textile products. It is particularly useful when using disperse dyes or when printing products made of mixed fabrics of polyamide and polyurethane fibers, which are susceptible to staining. Hereinafter, the present invention will be explained in detail with reference to Examples. Example 1 A polka dot pattern was printed on a polyester/cotton (65/35) mixed fabric using a color paste according to the following method using an autoscreen printing machine. DIANIX BLUE BG-FS 50g (Mitsubishi Kasei, acid separation dye) PROCION BLUE H-5R 20g (ICI, reactive dye) Urea 50g Soda ash 20g MS powder 30g (Meisei Chemical, reduction inhibitor) Sodium alginate NSPM 500g (solid content 10%, made by Kamogawa Kasei, sizing agent) 330g of warm water Total 1000g After drying this printed fabric at 100℃ for 2 minutes, dry it at 190℃.
Dye fixation was achieved by processing for 60 seconds. This printed fabric was washed with water and treated in a soaping bath according to the following A, B, and C treatments at a bath ratio of 1:40 at a temperature raised from 30°C to 80°C for 20 minutes.
【表】【table】
【表】
C処法では、50℃昇温後、ハイドロサルフアイ
トを添加した。
この処理布を下記処法の脱塩素浴で、60℃で20
分間処理した。
過酸化水素水(35%溶液) 5g/
ソーダ灰 1g/
得られた捺染製品の白場部分の最大吸収波長
620mμにおける反射率は、次の通りであり、分
散染料による白場汚染の防止効果は著るしいもの
であつた。
処理布 反射率(%)
原 布 84.3
A処法 75.6
B処法 82.4
C処法 84.0
また、湿摩擦と洗濯堅牢度は、それぞれA処法
に比べ0.5級、1級程度向上し、しかも、鮮明性
も向上したものであつた。
実施例 2
ポリエステル/ポリアミド(50/50)混繊糸織
物を下記処法の色糊を用いて、ハンドプリントに
て、水玉柄を印捺した。
SUMIKALON RED S―BL 40g
(住友化学製、分散染料)
メイプロガムNP(固型分12%) 600g
(メイプロ製、糊剤)
MSパウダー 30g
酒石酸(固型分50%) 10g
尿 素 50g
温 湯 270g
計 1000g
この印捺布を高圧スチマーにて、130℃で30分
間処理して、染料固着を行なつた。この捺染布を
水洗し、浴比1:40にて、下記D、E、F処法の
ソーピング浴にて、80℃で20分間処理した。[Table] In Process C, hydrosulfite was added after the temperature was raised to 50°C. This treated cloth was heated to 60℃ for 20 minutes in a dechlorination bath using the following method.
Processed for minutes. Hydrogen peroxide solution (35% solution) 5g/Soda ash 1g/Maximum absorption wavelength of the white area of the obtained printed product
The reflectance at 620 mμ was as follows, and the effect of preventing white field contamination by the disperse dye was remarkable. Treated fabric Reflectance (%) Original fabric 84.3 Process A 75.6 Process B 82.4 Process C 84.0 In addition, the wet friction and washing fastness were improved by about 0.5 and 1 grade compared to Process A, respectively, and the color was clear and clear. Her sexuality was also improved. Example 2 A polka dot pattern was printed by hand on a polyester/polyamide (50/50) mixed yarn fabric using colored paste according to the following method. SUMIKALON RED S-BL 40g (manufactured by Sumitomo Chemical, disperse dye) Maypro Gum NP (solid content 12%) 600g (manufactured by Maypro, glue) MS powder 30g Tartaric acid (solid content 50%) 10g Urea 50g Warm water 270g Total 1000 g of this printed fabric was treated with a high-pressure steamer at 130° C. for 30 minutes to fix the dye. This printed fabric was washed with water and treated at 80° C. for 20 minutes in a soaping bath according to the following D, E, and F treatments at a bath ratio of 1:40.
【表】
コンク
F処法では、80℃で20分間処理した後、ハイド
ロサルフアイトを添加し、5分間処理した。この
処理布を実施例1と同じ条件で脱塩素処理した。
得られた捺染製品の白場部分の最大吸収波長
540mμにおける反射率は、次の通りであり、分
散染料による白場の防止効果は著るしいものであ
つた。
処理布 反射率(%)
原 布 53.2
D処法 29.9
E処法 44.7
F処法 51.8
実施例 3
ポリアミド/ポリウレタン(50/50)からなる
編物を下記処法の色糊を用いて、ハンドプリント
にて、水玉柄を印捺した。
SANDLAN BRILLIANT RED N3B 140%
(SANDOZ製、酸性染料) 20g
グリエシンA 20g
(BASF製、染料溶解剤)
メイプロガムNP(固型分12%) 500g
(メイプロ製、糊剤)
硫酸アンモニウム 20g
熱 湯 440g
計 1000g
この印捺布を120℃で約60秒間乾燥し、常圧ス
チーマーにて、100℃で30分間処理して発色固着
を行なつた。次いでカセイソーダ(約44%濃度
品)2g/の浴でよく糊落しを行なつた後、下
記G、H、I処法のソーピング浴にて60℃で20分
処理した。[Table] In the Conch F treatment, after being treated at 80°C for 20 minutes, hydrosulfite was added and treated for 5 minutes. This treated cloth was subjected to dechlorination treatment under the same conditions as in Example 1. Maximum absorption wavelength of the white area of the obtained printed product
The reflectance at 540 mμ was as follows, and the effect of preventing white areas by the disperse dye was remarkable. Treated fabric Reflectance (%) Original fabric 53.2 D treatment 29.9 E treatment 44.7 F treatment 51.8 Example 3 A knitted fabric made of polyamide/polyurethane (50/50) was hand printed using colored glue according to the following formula. I printed a polka dot pattern on it. SANDLAN BRILLIANT RED N3B 140% (manufactured by SANDOZ, acid dye) 20g Gliescin A 20g (manufactured by BASF, dye solubilizer) Maypro Gum NP (solid content 12%) 500g (manufactured by Maypro, glue) Ammonium sulfate 20g Hot water 440g Total 1000g of this The printed fabric was dried at 120°C for about 60 seconds, and then treated with an atmospheric pressure steamer at 100°C for 30 minutes to develop and fix the color. Next, after thoroughly removing the starch in a bath containing 2 g of caustic soda (approximately 44% concentration product), it was treated at 60° C. for 20 minutes in a soaping bath of the following G, H, and I treatments.
【表】
I処法では、50℃に昇温後、ハイドロサルフア
イトを添加した。この処理布を実施例1と同じ条
件で脱塩素処理した。
得られた捺染物の白場部分の最大吸収波長
540mμにおける反射率は、次の通りであり、酸
性染料による汚染の少ない捺染物が得られた。
処理布 反射率(%)
原 布 65.3
G処法 42.1
H処法 58.4
I処法 63.6
また、この捺染物は、実施例1と同様に、湿摩
擦と洗濯堅牢度は、G処法に比べそれぞれ、1級
程度向上したものであつた。[Table] In Process I, hydrosulfite was added after the temperature was raised to 50°C. This treated cloth was subjected to dechlorination treatment under the same conditions as in Example 1. Maximum absorption wavelength of the white area of the obtained printed material
The reflectance at 540 mμ was as follows, and a printed material with little staining by acid dye was obtained. Treated fabric Reflectance (%) Original fabric 65.3 G treatment 42.1 H treatment 58.4 I treatment 63.6 Also, as in Example 1, this printed material had better wet rubbing and washing fastness than G treatment. , which was an improvement of about 1 grade.
Claims (1)
を染色した後、塩素系漂白剤を含有したアルカリ
性ソーピング浴で処理し、次いで還元漂白剤で処
理することを特徴とする繊維製品の後処理法。1. A post-treatment method for textile products, which comprises, after printing a fabric or dyeing a fabric mixed with different types of fibers, treating it with an alkaline soaping bath containing a chlorine bleach, and then treating it with a reducing bleach. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15686979A JPS5679787A (en) | 1979-12-05 | 1979-12-05 | Postttreatment of fiber product |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15686979A JPS5679787A (en) | 1979-12-05 | 1979-12-05 | Postttreatment of fiber product |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5679787A JPS5679787A (en) | 1981-06-30 |
| JPS6158596B2 true JPS6158596B2 (en) | 1986-12-12 |
Family
ID=15637161
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15686979A Granted JPS5679787A (en) | 1979-12-05 | 1979-12-05 | Postttreatment of fiber product |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5679787A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5649578B2 (en) * | 2009-08-25 | 2015-01-07 | 国立大学法人 東京大学 | Method for hydrophilic treatment of cellulose fiber and method for producing hydrophilic cellulose fiber |
| US9103065B2 (en) * | 2011-09-12 | 2015-08-11 | Gunze Limited | Method for producing hydrophilic cellulose fiber |
-
1979
- 1979-12-05 JP JP15686979A patent/JPS5679787A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5679787A (en) | 1981-06-30 |
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