JPH0742660B2 - Post-treatment method for dyeing textile materials containing cellulose fibers - Google Patents

Post-treatment method for dyeing textile materials containing cellulose fibers

Info

Publication number
JPH0742660B2
JPH0742660B2 JP62006874A JP687487A JPH0742660B2 JP H0742660 B2 JPH0742660 B2 JP H0742660B2 JP 62006874 A JP62006874 A JP 62006874A JP 687487 A JP687487 A JP 687487A JP H0742660 B2 JPH0742660 B2 JP H0742660B2
Authority
JP
Japan
Prior art keywords
fastness
dyed
post
dyeing
chitosan
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 - Fee Related
Application number
JP62006874A
Other languages
Japanese (ja)
Other versions
JPS63175186A (en
Inventor
元次 徳永
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DKS CO. LTD.
Original Assignee
DKS CO. LTD.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by DKS CO. LTD. filed Critical DKS CO. LTD.
Priority to JP62006874A priority Critical patent/JPH0742660B2/en
Publication of JPS63175186A publication Critical patent/JPS63175186A/en
Publication of JPH0742660B2 publication Critical patent/JPH0742660B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は直接染料及び/又は反応性染料を用いて染色し
たセルロース系繊維を含む繊維材料染色物の染色堅牢度
を向上させる後処理法に関する。
The present invention relates to a post-treatment method for improving the dyeing fastness of a dyeing of a fiber material containing a cellulosic fiber dyed with a direct dye and / or a reactive dye.

直接染料を用いて染色した被染物は、一般に耐洗濯堅牢
度、耐水堅牢度、耐汗堅牢度等の染色堅牢度が小さく、
そのままでは実用に供し得ない。
Dyeing products dyed with a direct dye generally have small dyeing fastness such as wash fastness, water fastness, sweat fastness, etc.
It cannot be put to practical use as it is.

また、反応性染料を用いて染色した被染物は、直接染料
による被染物に比較すると、染色堅牢度が優れている
が、それでも耐洗濯堅牢度、耐水堅牢度、耐汗堅牢度等
において、なお不充分であり、また繊維と反応性染料と
の共有結合が空気中で加水分解を受けて徐々に切断され
るために、時間とともに該被染物の染色堅牢度が低下す
る。このため反応性染料による被染物の場合において
も、このままでは実用に供し得ないことがある。かかる
理由により従来より被染物の染色堅牢度を向上させる目
的で染色後に特殊なカチオン性ポリマーの希薄水溶液に
より被染物を処理することが行なわれている。
Further, the dyed object dyed with the reactive dye is excellent in dyeing fastness as compared with the dyeing object using the direct dye, but still, in washing fastness, water fastness, sweat fastness, etc., Insufficiency, and since the covalent bond between the fiber and the reactive dye is hydrolyzed in the air to be gradually broken, the dyeing fastness of the dyed product decreases with time. Therefore, even in the case of an article to be dyed with a reactive dye, it may not be put to practical use as it is. For this reason, conventionally, for the purpose of improving the dyeing fastness of the dyed product, the dyed product is treated with a dilute aqueous solution of a special cationic polymer after dyeing.

このようなカチオン性ポリマーとしてジシアンジアミド
とホルマリンとの縮合物あるいはエチレンジアミン、ジ
エチレントリアミン等のポリアミンとジシアンジアミド
等との縮合物が主に用いられている。しかしながらこの
種のカチオン性ポリマーには、分子中に第4級アンモニ
ウム以外に第1級、第2級および第3級アミンが高濃度
で含まれているために被染物を処理した場合、処理によ
る変色が著しくなると同時に耐光堅牢度の低下を避ける
ことができないという欠点がある。さらに前者、すなわ
ち、ジシアンジアミドとホルマリンとの縮合物の場合に
は残留ホルマリンが問題となり、環境衛生の点で好まし
くない。
As such a cationic polymer, a condensate of dicyandiamide and formalin or a condensate of polyamine such as ethylenediamine and diethylenetriamine and dicyandiamide is mainly used. However, this type of cationic polymer contains a high concentration of primary, secondary, and tertiary amines in addition to quaternary ammonium in the molecule. There is a drawback in that discoloration becomes remarkable and at the same time, deterioration of light fastness cannot be avoided. Further, in the former case, that is, in the case of a condensate of dicyandiamide and formalin, residual formalin becomes a problem, which is not preferable from the viewpoint of environmental hygiene.

本発明の目的は、上記染色物の耐洗濯、耐水、耐汗、耐
光および耐摩擦堅牢度を向上させると共に、該処理後に
よっても何ら耐塩素水、耐汗、日光複合、蛍光増白耐光
堅牢度等を低下させない新しい後処理法を提供すること
にある。
The object of the present invention is to improve the wash resistance, water resistance, sweat resistance, light resistance and abrasion resistance of the dyed product, and even after the treatment, there is no chlorine water resistance, sweat resistance, sunlight composite, fluorescent whitening light resistance. It is to provide a new post-treatment method that does not reduce the degree of deterioration.

特に、反応性染料を用いて染色した被染物は直接染料に
よる被染物に比べると、一般にその染色堅牢度は優れて
いるが、それでも尚、耐洗濯堅牢度、耐水堅牢度、耐汗
堅牢度等において、不充分であり、また繊維と反応性染
料との共有結合が空気中で加水分解を受けて徐々に切断
されるために時間とともに該被染物の染色堅牢度が低下
するを避け得ない。
In particular, a dyed product dyed with a reactive dye is generally superior in dyeing fastness to a dyed product using a direct dye, but nevertheless, the washfastness, waterfastness, sweatfastness, etc. Is insufficient, and the covalent bond between the fiber and the reactive dye is hydrolyzed in the air and gradually cut, so that it is unavoidable that the dyeing fastness of the dyeing product decreases with time.

かかる理由により、上記反応性染料による染色の場合、
通常引き続き各種の固着剤を用いて後処理することがよ
く行なわれている。
For this reason, in the case of dyeing with the above reactive dye,
It is common practice to subsequently carry out post-treatments with various fixing agents.

本発明者は、上記後処理に用いられる固着剤につき、種
々研究を重ねた結果、甲殻類から得られるキトサンの酸
塩が、従来公知のこの種の固着剤に比較して、とくに耐
洗濯堅牢度、耐水堅牢度、耐汗堅牢度を顕著に向上させ
得る作用を有し、この種固着剤として極めて有効である
ことを見い出したものである。
The present inventor has conducted various studies on the sticking agent used in the above-mentioned post-treatment, and as a result, the salt of chitosan obtained from crustaceans is particularly wash-fast and fast as compared with the conventionally known sticking agent of this type. It has been found that it has the effect of remarkably improving the water resistance, the water fastness and the sweat fastness, and is extremely effective as this kind of fixing agent.

しかるに、近年染色業界においては染色物の品質向上に
対する要望が益々々高まり、上記反応性染料で染色した
場合被染物についても、従来の染色堅牢度に加えて、さ
らに下記各種の堅牢度をも具備する特性を要求されつつ
ある。
However, in the dyeing industry in recent years, there has been an increasing demand for improvement in the quality of dyed products, and when dyed with the above reactive dye, the dyed product also has the following various fastnesses in addition to the conventional dyeing fastness. The characteristics to do are being demanded.

耐塩素水堅牢度が低下しないこと 近年都市水道水中の活性塩素濃度はかなり高くなり、該
水道水により繰返し洗濯される被染物は、耐塩素水堅牢
度が要求される。これは、漂白剤を含む洗剤で洗濯され
る場合にも同様のことがいえる。
The resistance to chlorine water fastness does not decrease In recent years, the concentration of active chlorine in city tap water has increased considerably, and the dyeing product repeatedly washed with the tap water is required to have fastness to chlorine water. The same can be said when washing with a detergent containing a bleaching agent.

汗・日光複合堅牢度が低下しないこと 汗を含む染色物が、日光により変退色しやすいことが近
時問題となっている。
Permanent sweat / sunlight fastness has not deteriorated It has recently become a problem that dyes containing sweat easily discolor and fade due to sunlight.

蛍光増白耐光堅牢度が低下しないこと 捺染物の白場の白度を向上させるため、一般に蛍光増白
剤が用いられるが、該蛍光増白剤で処理された捺染物上
の反応性染料は日光により極めて変退色し易い。
Fluorescent whitening Fastness to light does not decrease In order to improve the whiteness of the printed article in the white field, a fluorescent whitening agent is generally used, but the reactive dye on the printed article treated with the fluorescent whitening agent is Very easily discolored by sunlight.

公知の後処理用固着剤は、いずれも上記〜の要求に
対しては全くこれらにつき考慮されておらず、もちろ
ん、これら要求に合致する性質を備えていない。
None of the known post-treatment fixing agents considers the above-mentioned requirements (1) to (3) and, of course, does not have the properties that meet these requirements.

むしろ公知の固着剤は、これらの利用によって上記〜
の堅牢度を必然的に低下させる傾向があった。
Rather, the publicly known adhesives have the above-mentioned properties due to their use.
Inevitably tended to reduce the fastness of.

従って、本発明者は、引続き、特に上記〜の堅牢度
の低下をも解消すべく、鋭意研究の結果、蟹、蝦等の甲
殻類に含まれるキトサンポリマーの酸塩が、上記〜
の堅牢度に対して極めて重大な影響を与えることを認
め、本発明を完成するに至ったものである。即ち、本発
明は 直接染料及び/又は反応性染料を用いて染色したセルロ
ース系繊維を含む繊維材料染色物の後処理法において、
キトサンの無機酸塩もしくは有機酸塩の水溶液を用いて
被染物を処理することを特徴とする染色堅牢度を向上さ
せるセルロース系繊維を含む繊維材料染色物の後処理法
を提供するものである。
Therefore, the present inventor continued to solve the deterioration of the fastness particularly in the above-mentioned, and as a result of earnest research, as a result, the acid salt of the chitosan polymer contained in the crustaceans such as crabs and reeds is
The present invention has been completed by recognizing that it has a very serious influence on the fastness of the. That is, the present invention provides a post-treatment method for a textile material dyeing product containing a cellulosic fiber dyed with a direct dye and / or a reactive dye,
The present invention provides a post-treatment method for a dyed textile material containing cellulosic fibers, which improves dyeing fastness, which comprises treating an article to be dyed with an aqueous solution of an inorganic acid salt or an organic acid salt of chitosan.

本発明において、キトサンの無機酸塩もしくは有機酸塩
の水溶液で被染物を処理する方法としては、特に限定は
なく、従来公知の方法を適宜使用できる。例えば、キト
サンの無機酸塩もしくは有機酸塩を繊維に対して、0.2
〜4.0重量%溶解した水溶液中に処理すべき被染物を所
定時間浸漬した後、水洗し、乾燥させるか、またはキト
サンの無機酸塩もしくは有機酸塩の0.2〜4.0重量%、必
要に応じて繊維加工樹脂及び/又は蛍光染料を含んだ溶
液で処理すべき染色物をパッド処理すればよい。
In the present invention, the method of treating the material to be dyed with an aqueous solution of an inorganic acid salt or an organic acid salt of chitosan is not particularly limited, and a conventionally known method can be appropriately used. For example, the mineral or organic acid salt of chitosan is added to the fiber at 0.2
~ 4.0% by weight of the dyed material to be treated in a dissolved aqueous solution for a certain period of time, followed by washing with water and drying, or 0.2 to 4.0% by weight of the inorganic or organic acid salt of chitosan, if necessary fiber The dyed product to be treated with the solution containing the processing resin and / or the fluorescent dye may be pad-treated.

浸漬処理の場合、浴比(被染物:水)は通常1:10〜20で
あり、処理温度は通常常温〜80℃であり、また処理時間
は通常5〜20分である。また、本発明に使用するキトサ
ンの無機酸塩もしくは有機酸塩の水溶液とは、キチン質
を脱アセチル化して得られるキトサンを無機酸塩もしく
は有機酸で塩タイプとした水溶液である。
In the case of the dipping treatment, the bath ratio (object to be dyed: water) is usually 1:10 to 20, the treatment temperature is usually room temperature to 80 ° C., and the treatment time is usually 5 to 20 minutes. Further, the aqueous solution of inorganic acid salt or organic acid salt of chitosan used in the present invention is an aqueous solution of chitosan obtained by deacetylating chitin and made into a salt type with an inorganic acid salt or an organic acid.

キトサンは、分子量が数千以上〜数十万以下で、甲殻類
の外殻、昆虫類の外皮成分、菌類の細胞壁等に多く存在
するキチンを濃厚アルカリ液で高温処理して得られるも
のである。
Chitosan has a molecular weight of several thousand or more to several hundred thousand or less, and is obtained by high-temperature treatment of chitin, which is often present in the shells of crustaceans, shell components of insects, cell walls of fungi, etc., with a concentrated alkaline solution. .

キトサンの塩を形成させるために使用する無機酸とは、
例えば、塩酸などであり、さらに有機酸とは、例えば、
蟻酸、酢酸などである。
The inorganic acid used to form the salt of chitosan is
For example, hydrochloric acid and the like, and the organic acid is, for example,
Formic acid, acetic acid, etc.

キトサン塩の水溶液は、前記キトサンに前記無機酸もし
くは有機酸を加えて、キトサン塩濃度2〜50重量%とし
た水溶液とするのが適当である。また、要すれば、低級
アルコール類等の水溶液に配合して用いてもよい。
The aqueous solution of chitosan salt is suitably an aqueous solution having the chitosan salt concentration of 2 to 50 wt% by adding the inorganic or organic acid to the chitosan. If necessary, they may be used by being mixed with an aqueous solution of lower alcohols.

次に、本発明を実施例により具体的に説明する。Next, the present invention will be specifically described with reference to examples.

実施例 氷酢酸0.3重量%および、キトサン0.5重量%からなる水
溶液を調製し、次いで、下記に示した染色物を処理し、
下記試験方法に従って、染色堅牢度を測定した。これら
の結果を第1表〜第5表に示した。
Example An aqueous solution consisting of 0.3% by weight of glacial acetic acid and 0.5% by weight of chitosan was prepared, and then the dyed product shown below was treated,
The dyeing fastness was measured according to the following test method. The results are shown in Tables 1 to 5.

1−染色物の調製 綿メリヤスを反応性染料および、直接染料にて常法に従
って染色し、次いでトライポールSR[第一工業製薬
(株)社製]の2g/1水溶液で90℃nにて10分間洗浄後、
水洗、乾燥した。
1-Preparation of dyed product A cotton knit is dyed with a reactive dye and a direct dye according to a conventional method, and then with a 2 g / 1 aqueous solution of Trypol SR [Daiichi Kogyo Seiyaku Co., Ltd.] at 90 ° C. After washing for 10 minutes,
It was washed with water and dried.

反応性染料 レマゾールブリリアントレッドBB (CI Reactive Red21) 3%o.w.f シバクロンブリリアントレッド4G−E (CI Reactive Red120) 1%o.w.f レマゾールブリリアントブル−R (CI Reactive Blue19) 4%o.w.f ダイアミラーターキスブルーB (CI Reactive Blue) 3%o.w.f レマゾールブラックB (CI Reactive Black5) 5%o.w.f 直接染料 カヤラススブラレッド6BL スミライトレッドF3B カヤラススプラターコイズブルーGL 1−堅牢度増進剤処理 本発明品および比較品を、浴比1:30で約60℃にて20分間
処理し、水洗した後乾燥した。
Reactive Dye Remazol Brilliant Red BB (CI Reactive Red21) 3% owf Cibacron Brilliant Red 4G-E (CI Reactive Red120) 1% owf Remazol Brilliant Bull-R (CI Reactive Blue19) 4% owf Diamirror Turkis Blue B (CI Reactive Blue) 3% owf Remazol Black B (CI Reactive Black5) 5% owf Direct dye Kayaras Subra Red 6BL Sumilite Red F3B Kayaras Supra Turquoise Blue GL 1-fastness enhancer treatment The comparative product was treated at a bath ratio of 1:30 at about 60 ° C. for 20 minutes, washed with water, and then dried.

1−堅牢度試験方法 (a)洗濯に対する染色堅牢度試験 JIS L−0844 A−3法(反応性染料) JIS L−1045 A−2法(直接染料) (b)汗に対する染色堅牢度試験 JIS L−0848 A法アルカリ性 (c)経時変化後の染色堅牢度試験 試験布をHPスチーマーにて115℃で60分間スチーミング
した後JIS L−0846 A法の水に対する染色堅牢度試
験に供する。
1-Fastness test method (a) Dyeing fastness test for washing JIS L-0844 A-3 method (reactive dye) JIS L-1045 A-2 method (direct dye) (b) Dyeing fastness test for sweat JIS L-0848 Method A alkaline (c) Dyeing fastness test after aging The test cloth is steamed with an HP steamer at 115 ° C. for 60 minutes, and then subjected to JIS L-0846 Method A dyeing fastness test with water.

(d)耐塩素堅牢度試験 有効塩素20ppm(次亜塩素酸ソーダ使用)の液に浴比1:2
00で室温にて2時間、試験布を浸漬する。
(D) Chlorine resistance fastness test A bath ratio of 1: 2 for a liquid containing 20 ppm of effective chlorine (using sodium hypochlorite)
Immerse the test cloth at 00 at room temperature for 2 hours.

(e)日光堅牢度試験 フェード・オ・メーターにて試験布を63℃で20時間露光
する。
(E) Sunlight fastness test The test cloth is exposed for 20 hours at 63 ° C with a fade-o-meter.

JIS L0842−1971 1−判定方法 染色堅牢度は添付白布(綿および絹)の汚染度を汚染用
グレースケールにて級数判定した。耐塩素堅牢度試験お
よび日光堅牢度試験は退色度を変色用グレースケールに
て級数判定した。
JIS L0842-1971 1-Judgment method For the dyeing fastness, the contamination degree of the attached white cloth (cotton and silk) was evaluated with a gray scale for contamination. In the chlorine fastness test and the sunlight fastness test, the degree of discoloration was evaluated by a gray scale for discoloration.

(注)なお、比較品として公知の湿潤堅牢度増進剤であ
る下記2品を供試した。
(Note) As a comparative product, the following two products, which are well-known wet fastness enhancers, were tested.

比較品:カチオン系高分子化合物を主成分とする堅牢
度増進剤0.5%水溶液 比較品:ポリアミン系カチオン樹脂を主成分とする堅
牢度増進剤0.5%水溶液 供試物:分子量約6万のキトサン[新日本化学(株)
社製]を使用 供試物:分子量約1万のキトサン[新日本化学(株)
社製]を使用
Comparative product: 0.5% aqueous solution of a fastness enhancer containing a cationic polymer as the main component Comparative product: 0.5% aqueous solution of a fastness enhancer containing a polyamine-based cationic resin as a test sample: Chitosan with a molecular weight of about 60,000 Shin Nippon Kagaku Co., Ltd.
Manufactured by Eisai Co., Ltd. Specimen: Chitosan with a molecular weight of about 10,000
Use]

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】直接染料及び/又は反応性染料を用いて染
色したセルロース系繊維を含む繊維材料染色物の後処理
法において、キトサンの無機酸塩もしくは有機酸塩の水
溶液を用いて被染物を処理することを特徴とする染色堅
牢度を向上させるセルロース系繊維を含む繊維材料染色
物の後処理法。
1. A method for post-treatment of a dyed textile material containing a cellulosic fiber dyed with a direct dye and / or a reactive dye, wherein the dyed material is treated with an aqueous solution of an inorganic acid salt or an organic acid salt of chitosan. A post-treatment method for a dyed textile material containing a cellulosic fiber, which is characterized in that the dyeing fastness is improved.
JP62006874A 1987-01-13 1987-01-13 Post-treatment method for dyeing textile materials containing cellulose fibers Expired - Fee Related JPH0742660B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62006874A JPH0742660B2 (en) 1987-01-13 1987-01-13 Post-treatment method for dyeing textile materials containing cellulose fibers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62006874A JPH0742660B2 (en) 1987-01-13 1987-01-13 Post-treatment method for dyeing textile materials containing cellulose fibers

Publications (2)

Publication Number Publication Date
JPS63175186A JPS63175186A (en) 1988-07-19
JPH0742660B2 true JPH0742660B2 (en) 1995-05-10

Family

ID=11650371

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62006874A Expired - Fee Related JPH0742660B2 (en) 1987-01-13 1987-01-13 Post-treatment method for dyeing textile materials containing cellulose fibers

Country Status (1)

Country Link
JP (1) JPH0742660B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5904738A (en) * 1998-01-28 1999-05-18 Crompton & Knowles Corporation Gas-fade inhibition
AT508846B1 (en) * 2009-09-17 2012-02-15 Chemiefaser Lenzing Ag FLUORESCENT FIBERS, THEIR USE AND METHOD FOR THE PRODUCTION THEREOF
EP2762556B1 (en) * 2011-09-28 2018-03-14 Jilin Hengtai Garment Washing And Dyeing Science And Technology Institute Color enhancing detergent for colored textile and preparation method therefor

Also Published As

Publication number Publication date
JPS63175186A (en) 1988-07-19

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