JPS6088190A - Printing of modified polyester/cellulose fiber blended structure - Google Patents
Printing of modified polyester/cellulose fiber blended structureInfo
- Publication number
- JPS6088190A JPS6088190A JP58194965A JP19496583A JPS6088190A JP S6088190 A JPS6088190 A JP S6088190A JP 58194965 A JP58194965 A JP 58194965A JP 19496583 A JP19496583 A JP 19496583A JP S6088190 A JPS6088190 A JP S6088190A
- Authority
- JP
- Japan
- Prior art keywords
- printing
- dye
- parts
- modified polyester
- fibers
- 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
- 238000007639 printing Methods 0.000 title claims description 28
- 229920000728 polyester Polymers 0.000 title claims description 21
- 229920003043 Cellulose fiber Polymers 0.000 title claims description 14
- 239000000975 dye Substances 0.000 claims description 26
- 239000000985 reactive dye Substances 0.000 claims description 18
- 239000000835 fiber Substances 0.000 claims description 17
- 238000010025 steaming Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 10
- 125000002091 cationic group Chemical group 0.000 claims description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 17
- 239000000986 disperse dye Substances 0.000 description 17
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000002253 acid Substances 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
- 239000003638 chemical reducing agent Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- 239000004202 carbamide Substances 0.000 description 4
- 238000010018 discharge printing Methods 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 239000003292 glue Substances 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- -1 alkylene glycol Chemical compound 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 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 2
- ORLGPUVJERIKLW-UHFFFAOYSA-N 5-chlorotriazine Chemical compound ClC1=CN=NN=C1 ORLGPUVJERIKLW-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- 101100002917 Caenorhabditis elegans ash-2 gene Proteins 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-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
- 238000004061 bleaching Methods 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000009998 heat setting Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000003752 hydrotrope Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920003987 resole Polymers 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical class OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 238000009991 scouring Methods 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 235000017550 sodium carbonate Nutrition 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- 125000004825 2,2-dimethylpropylene group Chemical group [H]C([H])([H])C(C([H])([H])[H])(C([H])([H])[*:1])C([H])([H])[*:2] 0.000 description 1
- WHYQMPJLTUMFFV-UHFFFAOYSA-N 2-(4-sulfophenoxy)benzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1OC1=CC=C(S(O)(=O)=O)C=C1 WHYQMPJLTUMFFV-UHFFFAOYSA-N 0.000 description 1
- HBLRZDACQHNPJT-UHFFFAOYSA-N 4-sulfonaphthalene-2,7-dicarboxylic acid Chemical compound OS(=O)(=O)C1=CC(C(O)=O)=CC2=CC(C(=O)O)=CC=C21 HBLRZDACQHNPJT-UHFFFAOYSA-N 0.000 description 1
- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000209761 Avena Species 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 229920001407 Modal (textile) Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- ZURAKLKIKYCUJU-UHFFFAOYSA-N copper;azane Chemical compound N.[Cu+2] ZURAKLKIKYCUJU-UHFFFAOYSA-N 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000006259 organic additive Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
Landscapes
- Coloring (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は変性ポリエステル・セルロース繊維混合構造物
の捺染法に関するものであり、更に詳しくは変性ポリエ
ステル・セルロース繊維混合構造物を分散染料および反
応性染料を用いて鮮明かつ堅牢に捺染する方法に関する
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for printing a modified polyester/cellulose fiber mixed structure, and more specifically, the present invention relates to a method for printing a modified polyester/cellulose fiber mixed structure using a disperse dye and a reactive dye. Concerning the method of printing.
従来、ポリエステル・セルロース繊維混用品の捺染は固
着が容易で、かつ安価な顔料捺染が主体となっており、
一部高級捺染品として分散染料および反応性染料を用い
たオーツ(−捺染または防抜染が採用されている。かか
る捺染法においては分散染料およびモノクロルトリアジ
ン系染料を用いて高温スチーミングにより1段で染色す
るか、または分散染料およびビニルスルホン系染料を用
いて高温スチーミング後アルカリショックもシくハコー
ルドフィック処理する2段染色で染料固着されている。Traditionally, printing of polyester/cellulose fiber mixed products has been mainly done using pigment printing, which is easy to fix and is inexpensive.
Oats (-printing or resist discharge printing) using disperse dyes and reactive dyes is used for some high-quality printed products. In this printing method, disperse dyes and monochlorotriazine dyes are used in one step by high-temperature steaming. The dye is fixed by two-step dyeing, or by high-temperature steaming using disperse dyes and vinyl sulfone dyes, followed by a cold fix treatment to avoid alkali shock.
しかしながら、かかる固着法では分散染料1反応性染料
共に固着率が低く、コスト高となるほか、高温スチーミ
ングにおいて分散染料による綿サイドの汚染を生じたり
反F3性染料の分解を生じる等の欠点があり、色合せが
難しく、かつ染ツラが悪い等の欠点があり、鮮明で濃色
かっ堅牢な捺染品を得ることは困難である。このような
欠点は染着濃度を向上しようとして尿素の如きヒドロト
ロープ剤を使用するとき一層助長される。However, in this fixing method, the fixation rate of both the disperse dye and the reactive dye is low, resulting in high cost. In addition, there are disadvantages such as contamination of the cotton side with the disperse dye and decomposition of the anti-F3 dye during high-temperature steaming. There are drawbacks such as difficulty in color matching and poor dyeing, making it difficult to obtain clear, dark, and durable printed products. These disadvantages are exacerbated when hydrotropes such as urea are used to increase dye density.
本発明者等は上記欠点を解決し、鮮明で1色かつ堅牢な
捺染品を得るべく鋭意研究の結果、不発明の捺染法に到
達した。すなわち1本発明はカチオン染料に対し常圧可
染性を有する変性ポリエステル繊維とセルロース繊維の
混合構造物に、分散染料と反応性染料を含む染液または
捺染糊を印捺または付与した後、96〜105℃の蒸熱
処理により染料固着することを特徴とする。The inventors of the present invention have conducted extensive research in order to solve the above-mentioned drawbacks and obtain clear, single-color, and durable printed products, and as a result, have arrived at an uninvented printing method. That is, 1 the present invention is a mixed structure of modified polyester fibers and cellulose fibers that are dyeable to cationic dyes under normal pressure, after printing or applying a dye solution or printing paste containing a disperse dye and a reactive dye, It is characterized by dye fixation by steaming treatment at ~105°C.
本発明において用いられる変性ポリエステル繊維として
は、カチオン染料に常圧可染性を示すポリエステル繊維
であり、更に詳しくはテレフタル酸またはそのエステル
形成性成分を主体(80モルチ以上)とする酸成分とエ
チレングリコール。The modified polyester fiber used in the present invention is a polyester fiber that is dyeable with cationic dyes under normal pressure. glycol.
テトラメチレングリコール、1,4−シクロヘキサンジ
メタツール等のグリコール成1分ヲ主体(80モル%以
上)とするグリコール成分とから得られステル形成性成
分(A)1〜6モルチと、(A)成分とアルキレンチレ
フタレ−1成成分以外の付加的成分(B)との合計3〜
20モルチを含有する変性ポリエステルを紡糸、延伸、
場合により熱セット、捲縮加工して得られる繊維が挙げ
られる。1 to 6 moles of a stellate-forming component (A) obtained from a glycol component mainly containing 1 mole (80 mole % or more) of a glycol component such as tetramethylene glycol or 1,4-cyclohexane dimetatool; The total of the components and the additional component (B) other than the alkylene thirephthalate-1 component is 3~
The modified polyester containing 20 molti was spun, stretched,
Examples include fibers obtained by heat setting and crimping depending on the case.
スルホン酸金属塩基含有エステル形成性成分(A)とし
ては5−ナトリウムスルホイソフタル酸、スルホコハク
酸、4−スルホナフタレン−2,7−ジカルボン酸、5
〔4−スルホフェノキシ〕イソフタル酸のような酸成分
のほかスルホン酸金属塩基含有グリコール等が例示され
るが、特に5−ナトリウムスルホイソフタル酸が好まし
い。また、付加的成分(B)としては、イソフタル酸、
アジピン酸、セパシン酸、グルタル酸のような酸成分、
ジエチレングリコール、ジエチレングリコール、分子量
1000以下のポリエーテルグリコールのようなグリコ
ール成分が挙げられるが、イソフタル酸やポリエーテル
グリコールが好ましく、就中一般式[I]で示されるポ
リエーテルグリコールが特に好ましい、1
HO(CiH2i0)m−R−0(−CjH+ jO−
)nH・・・・・−(x)(式中、Rは#、累数2〜2
0の2価の欠化水素基。The sulfonic acid metal base-containing ester-forming component (A) includes 5-sodium sulfoisophthalic acid, sulfosuccinic acid, 4-sulfonaphthalene-2,7-dicarboxylic acid, 5-sulfonic acid metal base-containing ester-forming component (A),
In addition to acid components such as [4-sulfophenoxy]isophthalic acid, glycols containing sulfonic acid metal bases are exemplified, and 5-sodium sulfoisophthalic acid is particularly preferred. Further, as the additional component (B), isophthalic acid,
Acid components such as adipic acid, sepacic acid, and glutaric acid,
Glycol components such as diethylene glycol, diethylene glycol, and polyether glycol having a molecular weight of 1000 or less may be mentioned, but isophthalic acid and polyether glycol are preferable, and polyether glycol represented by the general formula [I] is particularly preferable. CiH2i0)m-R-0(-CjH+ jO-
)nH...-(x) (in the formula, R is #, cumulative number 2 to 2
0 divalent truncated hydrogen group.
rn+nは同一または異なる整数で1≦m+n≦15、
++3は2〜4の整数である)
なお、(B)成分は酸成分に対し2モルチ以上であるこ
とが好ましい。(B)成分は共重合成分として添加する
ことなくポリエステルの重縮合工程においてアルキレン
グリコールが縮合して生成して上の高速で紡糸すること
により常圧可染性を付4することができる。rn+n is the same or different integer, 1≦m+n≦15,
++3 is an integer from 2 to 4) Note that the component (B) is preferably 2 molti or more relative to the acid component. Component (B) is produced by condensation of alkylene glycol in the polyester polycondensation step without being added as a copolymerization component, and can be imparted with atmospheric dyeability by spinning at high speed.
上記式CI)におけるRの具体例としては、たとえば(
−CHz+aのような直鎮状脂肪族炭化水素基。As a specific example of R in the above formula CI), for example (
A straight aliphatic hydrocarbon group such as -CHz+a.
Hs
水素基などが挙げられる。変性ポリエステル繊維はステ
ーブル、フィラメントのいずれでもよく、またフラット
ヤーン、捲縮ヤーンいずれでもよい。Examples include Hs hydrogen group. The modified polyester fiber may be either stable or filament, and may be either flat yarn or crimped yarn.
また、これらの混合繊維でもよく、断面形状も円形、異
形いずれでもよい。更に変性ポリエステルの製造時また
l’を製造後における任意の段階で種々 5−
配合剤たとえばシリカ、クレー、カオリン、炭酸カルシ
ウムのような無機フイフー、ポリアルキレンクリコール
、有機のリン酸エステル塩、スルホン酸塩のような有機
添加剤等を配合した繊維であってもよい。Further, the fibers may be a mixture of these fibers, and the cross-sectional shape may be either circular or irregular. Furthermore, during the production of the modified polyester or at any stage after the production of l', various compounding agents such as silica, clay, kaolin, inorganic fibers such as calcium carbonate, polyalkylene glycols, organic phosphate ester salts, and sulfones may be added. Fibers containing organic additives such as acid salts may also be used.
また1本発明において用いられるセルロース繊維として
は、綿、麻のような天然セルロース繊維。Furthermore, the cellulose fibers used in the present invention include natural cellulose fibers such as cotton and linen.
ビスコースレーヨン、ホリノジツクレーヨン、銅安レー
ヨンのような再生セルロース繊維等が挙げられ、ステー
ブル、フィラメント等任意でよい。Examples include regenerated cellulose fibers such as viscose rayon, holinozytsu crayon, and copper ammonium rayon, and any suitable fibers such as stable and filament fibers may be used.
これらの繊維混合構造物としては、糸条物、細緻物、不
織布、敷物、テープ、立毛布などが挙げられ、混合の形
態としては混紡、混繊、交編織、多重構造布等のほか、
カバーヤーンのような複合糸およびそれらを用いた任意
の構造物が挙げられる。These fiber mixed structures include yarns, fine materials, non-woven fabrics, rugs, tapes, raised blankets, etc., and the mixed forms include blends, mixed fibers, mixed knitting and weaving, multilayer structure fabrics, etc.
Composite yarns such as cover yarns and any constructions using them are included.
本発明における捺染法を説明すると、オーバー捺染にお
いては、所望により親和性染料によって地染され次構遺
物に分散染料および反F3性染料を含有する染液または
捺染糊を印捺または部分付与した後1通常乾燥し、次い
で固着処理を行う。ま6−
た、防抜染においては上記染液または捺染糊を印捺また
は付与した後、通常乾燥してからアルカリ剤、還元剤な
どを含有する溶液または糊を印捺または部分付与するか
、もしくはアルカリ剤、還元剤等を含有する溶液または
糊を印捺または部分付与した後1通常乾燥し2次いで分
散染料および反応性染料を含有する染液または捺染糊を
印捺または付与した後1通常乾燥してから固着処理を行
う。To explain the printing method in the present invention, in overprinting, after dyeing with an affinity dye if desired, the dye liquid or printing paste containing a disperse dye and an anti-F3 dye is printed or partially applied to the next structure. 1. Usually dried and then fixed. In addition, in anti-discharge printing, after printing or applying the above-mentioned dye liquid or printing paste, printing or partially applying a solution or paste containing an alkaline agent, reducing agent, etc. after drying, or After printing or partially applying a solution or paste containing an alkali agent, reducing agent, etc., 1. Normally drying. 2. Next, printing or applying a dye solution or printing paste containing a disperse dye and a reactive dye. 1. Normally drying. Then perform the fixing process.
防抜染においてはアルカリ剤や還元剤を含有する液また
は糊中にはアルカリ剤や還元剤に安定な分散染料1反応
性染料(置換型)を配合してもよい。In resist discharge printing, a disperse dye 1-reactive dye (substitution type) that is stable to an alkali agent or reducing agent may be blended into the liquid or paste containing the alkaline agent or reducing agent.
切抜用染料としては1分散染料ではアルカリ剤により分
解または可溶化型染料1反応性染料では付加型反応性染
料が通常用いられる:1゜かかるオーバー捺染もしくは
防抜染における固着処理条件として、本発明においては
96〜105℃の常圧スチーミングを適用するのが必須
である。時間は通常5〜60分間程度であり、特に20
〜45分間が好ましい。As dyes for cutting out, 1 disperse dyes are decomposed or solubilized by alkaline dyes 1 reactive dyes are addition type reactive dyes; It is essential to apply normal pressure steaming at 96 to 105°C. The time is usually about 5 to 60 minutes, especially 20 minutes.
~45 minutes is preferred.
本発明においては、かかる条件を採用することにより常
圧でポリエステル繊維とセルロース繊維を一度に固着す
ることができるが、高温スチーミングによる固着と異な
り反応性染料の分解および分散染料のセルロース繊維へ
の汚染を防止することができ、それに供って鮮明かつ濃
色、堅牢な捺染品を得ることができる。常圧スチーミン
グによって反応性染料の固着に必要な水分を十分に得る
ことができることおよび多くの場合ヒドロトロープ剤の
添加も不要ガこと等もセルロース繊維への反応性染料の
固M率をより一層向上させるのに有効である。これらの
効果によりより鮮明な捺染や十分な白抜ができるなど品
質面のみならず、操業面、装置面およびコスト面などの
全ての点において利点は顕著である。In the present invention, by adopting such conditions, polyester fibers and cellulose fibers can be fixed at once under normal pressure, but unlike fixing by high-temperature steaming, the decomposition of the reactive dye and the dispersion of the disperse dye to the cellulose fiber occur. Contamination can be prevented, and as a result, printed products that are clear, dark, and durable can be obtained. The fact that atmospheric pressure steaming can obtain sufficient moisture necessary for the fixation of reactive dyes, and in many cases does not require the addition of hydrotropes, further improves the solidity M rate of reactive dyes on cellulose fibers. It is effective for improving These effects have remarkable advantages not only in terms of quality, such as clearer printing and sufficient whiteout, but also in terms of operation, equipment, and cost.
更に風合が柔軟なことも大きな特長である。染色前アル
カリ処理することにより効果をより助長することも可能
である。捺染後は常法によって洗浄、仕上げ処理される
が、柔軟剤処理、シリコーン系または/および弗素系撥
水剤処理、ポリエステルポリエーテル系防汚剤、その他
各種処理剤による処理により所望の性能を付与すること
ができる0
以下、実施例により本発明を説明する。なお、実施例中
の部および%は重量部および重量%を意味する。Another great feature is that it has a flexible texture. It is also possible to enhance the effect by alkali treatment before dyeing. After printing, it is washed and finished by conventional methods, but the desired performance is imparted by treatment with softeners, silicone-based and/or fluorine-based water repellents, polyester polyether-based antifouling agents, and various other processing agents. The present invention will be described below with reference to Examples. Note that parts and % in the examples mean parts by weight and % by weight.
実施例1゜
全酸成分に対し、5−ナトリウムスルホイソフタル酸成
分3モル%、一般式[I]におけるRが2.2−ジメチ
ルプロピレン基でありm 十n = 4 *i+j=5
のグリコール成分2モルチおよびジエチレングリコール
成分1.8モル饅を含有するエチレンテレフタレートを
常法により紡糸、延伸および熱セットして得られた変性
ポリエステル繊維ステープルと綿との混紡糸(30;
70重量比)からなるブロードクロスを常法により精練
、漂白した後、下記処方の染液(A)によりパッド、予
備乾燥した。Example 1 5-sodium sulfoisophthalic acid component is 3 mol % based on the total acid component, R in the general formula [I] is a 2,2-dimethylpropylene group, m 10n = 4 *i + j = 5
A blended yarn (30;
After scouring and bleaching a broadcloth consisting of (70% by weight) in a conventional manner, it was padded and pre-dried with a dye solution (A) having the following formulation.
染液(A)
Dispersol Black 2R−PC13部(
ICI社 分散染料)
9−
Remazol Black B 、 6部(ヘキスト
社 反応性染料)
アルギン酸ソーダ(5%) 5部
イルガゾールP 2部
(チバ ガイギー社 キャリヤー)
レマゾールソルトFD 2部
(ヘキスト社 アルカリ剤)
尿 素 2部
水 70部
次いで下記糊(B)を印捺乾燥した後% 105℃30
分間のスチーミングを行い、常法によりソーピングした
。Dye solution (A) Dispersol Black 2R-PC 13 parts (
ICI (disperse dye) 9- Remazol Black B, 6 parts (Hoechst reactive dye) Sodium alginate (5%) 5 parts Irgasol P 2 parts (Ciba Geigy carrier) Remazol Salt FD 2 parts (Hoechst alkaline agent) Urea 2 parts Water 70 parts Next, after printing and drying the following glue (B) % 105℃30
Steaming was carried out for 1 minute, and soaping was carried out in a conventional manner.
糊(B)
Sf(−2Q(第−工業製薬社 CMC) (10%9
4.5部しジストールHWS 3部
(明成化学社 抜染助剤)
カラーファインAD 6部
(第−工業製薬社 グリコール系助剤)スーパーライト
0 2部
(住友化学社 還元剤)
10−
ユビテツクスE B F O,5部
(チバ ガイギー社 分散螢光増白剤)ソーダ灰 2部
水 82部
その結果、未変性ポリエチレンテレフタレート・セルロ
ース繊維混の高圧スチーミングで到底得ることのできな
い鮮明性、型際尖鋭性を有する優分散染料汚染もなく1
色再現性が良好な、かつ堅牢染色品であった。Glue (B) Sf (-2Q (Dai-Kogyo Seiyaku Co., Ltd. CMC) (10%9
4.5 parts Dystol HWS 3 parts (Meisei Chemical Co., Ltd., discharge printing aid) Color Fine AD 6 parts (Dai-Kogyo Seiyaku Co., Ltd., glycol-based aid) Superlight 0 2 parts (Sumitomo Chemical Co., Ltd., reducing agent) 10- Ubitex E B FO, 5 parts (Ciba Geigy Dispersed fluorescent brightener) Soda ash 2 parts Water 82 parts As a result, the clarity and mold edge sharpness that cannot be obtained by high-pressure steaming of unmodified polyethylene terephthalate and cellulose fiber blends are obtained. No staining due to highly dispersed dyes 1
It was a fast dyed product with good color reproducibility.
実施例2゜
全酸成分に対し、5−ナトリウムスルホイソフタル酸成
分2.2モル饅、イソフタル酸成分10モルチおよびジ
エチYングリコール成分1.7モル%を含有する変性ポ
リエステルを引取り速度3000m/分の速度で紡糸し
た後延伸、熱セットして得られた変性ポリエステル繊維
ステープルと綿との混紡糸(50: 50重量比)から
なるブロードクロスを常法により精練、漂白した後、下
記処方の捺染糊(C)および(D)を用いてスクリーン
プリント機により2色柄を印捺した。Example 2 A modified polyester containing 2.2 mol% of 5-sodium sulfoisophthalic acid component, 10 mol% of isophthalic acid component, and 1.7 mol% of diethyl glycol component, based on the total acid components, was taken at a speed of 3000 m/ A broadcloth consisting of a blended yarn (50:50 weight ratio) of modified polyester fiber staple and cotton (50:50 weight ratio) obtained by spinning, stretching and heat setting at a speed of 30 minutes was scoured and bleached using a conventional method. A two-color pattern was printed using a screen printing machine using printing pastes (C) and (D).
捺染糊(C)
Sumifix Br111.Red BS 5部(住
友化学社 反応性染料)
Kayala、n Po1yester RD−5pa
ste 5部(日本化薬社 分散染料〕
5H−20(10%) 45部
レしゾールソルトFD 2部
イルガゾールP 1部
尿 素 5部
水 37部
捺染糊(D)
Remazol Br111.Yellow GGL
4部(ヘキスト社 反応性染料〕
Kayalan Po1yester LightYe
llow 5G8 4部
(日本化薬社 ビニルスルホン型分散染料〕5H−20
(10%) 45部
レしゾールソルトFD 2部
イルガゾールP 1部
尿 素 5部
水 39部
次いで乾燥してから105℃で40分間スチーミングし
、80℃5分間ソーピングした。Printing paste (C) Sumifix Br111. Red BS 5 parts (Sumitomo Chemical Co., Ltd. reactive dye) Kayala, n Polyester RD-5pa
ste 5 parts (Nippon Kayaku Co., Ltd. disperse dye) 5H-20 (10%) 45 parts Resol Salt FD 2 parts Irgazol P 1 part Urea 5 parts Water 37 parts Printing paste (D) Remazol Br111.Yellow GGL
4 parts (Hoechst reactive dye) Kayalan Polyester LightYe
low 5G8 4 parts (Nippon Kayakusha vinyl sulfone type disperse dye) 5H-20
(10%) 45 parts Resol Salt FD 2 parts Irgasol P 1 part Urea 5 parts Water 39 parts Then, after drying, it was steamed at 105°C for 40 minutes and soaped at 80°C for 5 minutes.
その結果、白湯の汚染もなく、鮮明かつ堅牢な両繊維サ
イドが一段で染料固着された赤、黄21!Sのプリント
布が得られた。As a result, there is no hot water contamination, and the dye is fixed on both sides of the bright and strong fibers in one step, red and yellow 21! A printed fabric of S was obtained.
実施例3゜
実施例1で用いた変性ポリエステル繊維とポリノジック
ステーブルとの混紡糸(65;35重量比)からなるブ
ロードクロスを常法により精練、漂白した後、下記処方
の染液(E)によりパッドし。Example 3 After scouring and bleaching a broadcloth made of a blended yarn (65:35 weight ratio) of modified polyester fiber and polynosic table used in Example 1 in a conventional manner, a dye solution (E) having the following formulation was applied. Due to padding.
予備乾燥した。Pre-dried.
染液(E)
Kayalan Po1yester Red BD−
8paste 4部(ヘキスト社 分散染料)
Sumifix Br111.Red BS 4部(住
友化学社 反応性染料)
アルギン酸ソーダ(5%) 50部
13−
イルガゾールP 1部
水 41部
次いで、下記糊(F)を印捺、乾燥後、105℃で35
分間スチーミングを行い、更に常法のコールドフィック
ス法により3時間エイジングし友後、水洗、乾燥した。Dye solution (E) Kayalan Polyester Red BD-
8paste 4 parts (Hoechst disperse dye) Sumifix Br111. Red BS 4 parts (Sumitomo Chemical Co., Ltd. reactive dye) Sodium alginate (5%) 50 parts 13- Irgazol P 1 part Water 41 parts Next, the following glue (F) was printed, dried, and heated at 105°C for 35 minutes.
Steaming was performed for a minute, and then aged for 3 hours using a conventional cold fix method, followed by washing with water and drying.
糊(F)
SH−20(10%) 45部
レしストールHWS a部
カラーファインAD 8部
Dianix Yellow H2G−FS 5部(三
菱化成社 分散染料〕
Kayacion Yellow P−4G 5部(日
本化薬社 モノクロルトリアジン型反応性染料)ソーダ
灰 2部
水 32部
その結果、きわめて鮮明な差色抜染布が得られた。また
、高温スチーミングによる固着で見られる反応性染料の
固着効率の低さから生じるカラーイール・ド不足もなく
濃色、堅牢なプリント品であ14−
つた。Glue (F) SH-20 (10%) 45 parts Restall HWS a part Color Fine AD 8 parts Dianix Yellow H2G-FS 5 parts (Mitsubishi Kasei Co., Ltd., disperse dye) Kayacion Yellow P-4G 5 parts (Nippon Kayaku Co., Ltd.) (monochlorotriazine type reactive dye) Soda ash 2 parts Water 32 parts As a result, a discharge-printed fabric with extremely clear difference colors was obtained.Also, the problem arises from the low fixation efficiency of reactive dyes seen in fixation by high-temperature steaming. There was no shortage of color yield, and the print was dark and sturdy.
−15− 609−-15- 609-
Claims (1)
ル繊維とセルロース繊維の混合構造物に1分散染料と反
応性染料を含む染液または捺染糊を印捺または付与した
後、96〜105℃の蒸熱処理により染料固着すること
を特徴とする変性ポリエステル・セルロース繊維混合構
造物の捺染法0After printing or applying a dye solution or printing paste containing a monodisperse dye and a reactive dye to a mixed structure of modified polyester fibers and cellulose fibers that are dyeable to cationic dyes under normal pressure, steaming at 96 to 105°C is performed. A method for printing a modified polyester/cellulose fiber mixed structure characterized by dye fixation by heat treatment0
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58194965A JPS6088190A (en) | 1983-10-18 | 1983-10-18 | Printing of modified polyester/cellulose fiber blended structure |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58194965A JPS6088190A (en) | 1983-10-18 | 1983-10-18 | Printing of modified polyester/cellulose fiber blended structure |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6088190A true JPS6088190A (en) | 1985-05-17 |
Family
ID=16333275
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58194965A Pending JPS6088190A (en) | 1983-10-18 | 1983-10-18 | Printing of modified polyester/cellulose fiber blended structure |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6088190A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62215082A (en) * | 1986-03-15 | 1987-09-21 | 東洋紡績株式会社 | Multicolor dyeing knitted fabric |
| DE102019000890A1 (en) | 2018-02-14 | 2019-08-14 | Fanuc Corporation | A robot system for executing learning control based on machining results and control method thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5813741A (en) * | 1981-07-17 | 1983-01-26 | 旭化成株式会社 | Polyester fiber/cellulosic faber blended knitted fabric |
| JPS58174691A (en) * | 1982-04-06 | 1983-10-13 | 住友化学工業株式会社 | Dyeing or printing of polyester/cellulose blended product |
-
1983
- 1983-10-18 JP JP58194965A patent/JPS6088190A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5813741A (en) * | 1981-07-17 | 1983-01-26 | 旭化成株式会社 | Polyester fiber/cellulosic faber blended knitted fabric |
| JPS58174691A (en) * | 1982-04-06 | 1983-10-13 | 住友化学工業株式会社 | Dyeing or printing of polyester/cellulose blended product |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62215082A (en) * | 1986-03-15 | 1987-09-21 | 東洋紡績株式会社 | Multicolor dyeing knitted fabric |
| DE102019000890A1 (en) | 2018-02-14 | 2019-08-14 | Fanuc Corporation | A robot system for executing learning control based on machining results and control method thereof |
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