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JPS6312198B2 - - Google Patents
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JPS6312198B2 - - Google Patents

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Publication number
JPS6312198B2
JPS6312198B2 JP60193199A JP19319985A JPS6312198B2 JP S6312198 B2 JPS6312198 B2 JP S6312198B2 JP 60193199 A JP60193199 A JP 60193199A JP 19319985 A JP19319985 A JP 19319985A JP S6312198 B2 JPS6312198 B2 JP S6312198B2
Authority
JP
Japan
Prior art keywords
dyeing
product
bath
mol
wrinkles
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
Application number
JP60193199A
Other languages
Japanese (ja)
Other versions
JPS6253484A (en
Inventor
Kenichi Kaeryama
Katsuyasu Myata
Motoharu Hasegawa
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.)
Nikka Chemical Industry Co Ltd
Original Assignee
Nikka Chemical Industry 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 Nikka Chemical Industry Co Ltd filed Critical Nikka Chemical Industry Co Ltd
Priority to JP60193199A priority Critical patent/JPS6253484A/en
Publication of JPS6253484A publication Critical patent/JPS6253484A/en
Publication of JPS6312198B2 publication Critical patent/JPS6312198B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、ポリアミド系繊維又はこれを含む繊
維製品の浴中品質向上剤に関する。更に詳しく
は、本発明は、該繊維製品の精練、染色等の浴中
処理の際に生じる、繊維製品の損傷、スレ、アタ
リ、シワなどによるトラブルを防止し、品位の高
い精練、染色加工を可能とするところの浴中品質
向上剤に関するものである。 〔従来の技術〕 従来、ナイロンに代表されるポリアミド繊維は
80〜100℃の高温の液中で精練、染色を行なう場
合、折れじわ、ロープじわ、スレ、アタリ等の現
象が見られ、品質に悪影響を及ぼす。そこで、ナ
イロンタフタに代表される織物の加工は、拡布状
で行なうジツカー染色等が一般的であり、近年増
加している液流染色は、シワ状の外観を付与する
“シワ加工”に応用されているのが現状である。
また、織物の加工においても、拡布状で行なわ
れ、ビーム染色等が一般的であり、液流染色は一
部で行なわれているにすぎない。 ナイロンの染色は、本来、90〜100℃にて行な
うのが一般的であるが、液流染色ではシワの発生
が少ない70℃以下の温度にて行なわれる。しか
し、この様な低温染色においては、染料のビルド
アツプが上がらず、また染色堅牢度にも問題が生
じる。 〔発明が解決しようとする問題点〕 この様な状況下で、近年普及している液流染色
機にてポリアミド繊維を精練、染色するために、
浴中品質向上剤なるものが使用されている。これ
には、ラノリン系乳化分散物、ポリエチレングリ
コール、ラノリン脂肪酸エステル等の長鎖アルキ
ル脂肪酸系及びポリエチレングリコールと多価カ
ルボン酸との水溶性ポリエステル化合物、エチレ
ンオキサイド付加水溶性ポリアミド化合物等の水
溶性高分子系があるが、前者はその効果が弱く、
処理浴での安定性にも問題があり、付着汚れや染
色斑等の欠点をも生じる。一方、後者はビルドア
ツプの低下や染料との凝集を起すなどの欠点があ
つて、いづれも充分なものではない。 本発明者等は上記の様な欠点のない、ポリアミ
ド繊維を80〜90℃にて液流染色加工の出来る浴中
品質向上剤に関し鋭意検討した結果、本発明を完
成したものである。 〔問題点を解決するための手段〕 本発明は、即ち、下記一般式で示される化合
物の少なくとも1種からなる事を特徴とするポリ
アミド系繊維用品質向上剤を提供する。 H〔−NHC3H6O(−C2H4O)−oC3H6NHCO−A−
CO〕−lOH (上式中、Aは−C6H4−、又は(−CH2)−nであ
り、ここでmは2〜8の整数であり、nは10〜90
の整数、lは1〜10の整数を表わす。) 本発明の式の化合物は一般式 H2NC3H6O(−C2H4O)−oC3H6NH2(n=10〜90) で表わされるジアミン類とジカルボン酸類、例え
ば、テレフタル酸、テレフタル酸ジメチル、ビス
−β−ヒドロキシエチルテレフタレート、ビス−
β−ヒドロキシテレフタレート、フタル酸等の芳
香族カルボン酸類、或いはコハク酸、アジピン
酸、セバチン酸、クエン酸等の脂肪酸カルボン酸
類とから縮合反応して得られるもので、反応は通
常の方法にて行なえばよい。 本発明を実施するには、式の化合物をポリア
ミド繊維に対し0.01〜5%、好ましくは、0.05〜
1%owf使用し、処理浴に添加して加工する事に
より行なう事が出来る。 式の化合物は優れた防しわ効果を示すと共
に、浴中に於ても良好な柔軟平滑性を付与するた
め、布同志あるいは布と機械(金属)との間の接
触摩擦抵抗を低下させ、繊維の表面を保護するた
め、しわの防止と共にスレ、アタリ等の防止効果
をも有する。一方、染色性にも影響を与えず、ビ
ルドアツプの低下も来たさない。また低起泡性で
あつて、作業性も良好なため、液流染色機にて80
〜90℃の温度で染色加工を行うことを可能ならし
めるものである。 実施例 以下に、例をもつて、本発明を更に説明する。 合成例 1 PEG#600のジプロピルアミノ化物71.4部(0.1
モル)とビス−β−ヒドロオキシエチルテレフタ
レート(以下B.H.E.Tと略)34.0部(0.125モル)
を減圧反応容器に仕込み、N2−gas置換し、130
℃まで加熱し、減圧にしながら、205℃±5℃に
て4時間(減圧度10−20mmHg)反応させ、その
後冷却し、反応を完了させ(反応物全アミン価
HClO4法8.1)、次いで温水368部を加えて反応物
を完全に溶解し、酢酸にてPH6.5に調整し、有効
濃度20%の発明品〔1〕を得た。20℃での粘度は
56c.p(B型粘度計)であつた。 合成例 2 PEG#1000のジプロピルアミノ化物111.4部
(0.1モル)とB.H.E.T34.0部(0.125モル)を仕込
み、合成例1と同様に反応させた生成物の全アミ
ン価は5.3であつた。 例1と同様に20%水溶液を調整した。粘度は
109c.pで、これを発明品〔2〕とした。 合成例 3 PEG#4000のジプロピルアミノ化物1029(0.25
モル)とBHET85部(0.3モル)とを仕込み、合
成例1と同様に反応させた生成物の全アミン価は
5.6であつた。 例1と同様にこの生成物の20%水溶液を調整し
た。粘度は93c.pでこれを発明品〔3〕とした。 合成例 4 PEG#1000のジプロピルアミノ化物111.4部
(0.1モル)とセバシン酸22.2部(0.11モル)とを
仕込み、合成例1と同様に反応させた生成物の全
アミン価は4.8であつた。 例1と同様にこの生成物の20%水溶液を調整し
た。粘度は46c.pで、これを本発明品〔4〕とし
た。 合成例 5 PEG#1000のジプロピルアミノ化物111.4部
(0.1モル)とアジピン酸16.1部(0.11モル)とを
仕込み、合成例1と同様に反応させた生成物の全
アミン価は3.7であつた。 例1と同様にこの生成物の20%溶液を調整し
た。粘度は112c.pで、これを本発明品〔5〕とし
た。 この様にして得られた本発明品〔1〕〜〔5〕
について、以下の実施例の中でその効果を参考品
と比較する。 実施例 1 ミニゼツト液流染色試験機(テキサム技研製)
を用い、精練処理したナイロンタフタ180cm×120
cm(タテ×ヨコ)140gに水5500ml(浴比1:
40:染色系本体での浴比1:5〜10、液流ポンプ
パイプ内の染液を入れると浴比1:40)を入れ、
染料としてKayanol Mill.Blue GW0.3%owfを
用い、浴中品質向上剤2g/を加え、評価した。
染色温度は20℃より2℃/分で昇温し、80℃×30
分及び90℃×30分染色し、その後急冷し、70℃に
て排液し、水洗を2回行つて、脱水、乾燥(75
℃)した。染色中の泡立量、乾燥生地のシワ発生
状態及びビルドアツプを肉眼で観察し、評価し
た。更に、風合(柔軟性)も触感にて比較した。
[Industrial Field of Application] The present invention relates to a bath quality improver for polyamide fibers or textile products containing the same. More specifically, the present invention prevents troubles such as damage, scuffing, sagging, and wrinkles of textile products that occur during bath processing such as scouring and dyeing of the textile products, and enables high-quality scouring and dyeing processing. The present invention relates to a quality improver in a bath that makes it possible to improve quality in a bath. [Conventional technology] Conventionally, polyamide fibers such as nylon
When scouring and dyeing are carried out in a high temperature solution of 80 to 100°C, phenomena such as creases, rope creases, scratches, and smudges are observed, which adversely affects quality. Therefore, when processing textiles such as nylon taffeta, it is common to use Zitzker dyeing, which is performed in the form of a spread cloth, and liquid jet dyeing, which has been increasing in recent years, is applied to "wrinkle processing" that gives a wrinkled appearance. The current situation is that
Furthermore, in the processing of textiles, it is generally carried out in the form of a spread cloth, and beam dyeing and the like are common, and jet dyeing is only partially carried out. Nylon dyeing is normally carried out at a temperature of 90 to 100°C, but jet dyeing is carried out at a temperature of 70°C or lower, where wrinkles are less likely to occur. However, such low-temperature dyeing does not increase the build-up of the dye and also causes problems in color fastness. [Problems to be solved by the invention] Under these circumstances, in order to scouring and dyeing polyamide fibers using a jet dyeing machine that has become popular in recent years,
A bath quality improver is used. These include lanolin-based emulsified dispersions, polyethylene glycol, long-chain alkyl fatty acid esters such as lanolin fatty acid esters, water-soluble polyester compounds of polyethylene glycol and polyhydric carboxylic acids, and water-soluble highly water-soluble polyamide compounds such as ethylene oxide-added water-soluble polyamide compounds. There are molecular systems, but the former has weak effects;
There are also problems with stability in processing baths, and disadvantages such as adhesion and staining occur. On the other hand, the latter has drawbacks such as reduced build-up and aggregation with dyes, and neither of these is sufficient. The present inventors have completed the present invention as a result of extensive research into an in-bath quality improver that does not have the above-mentioned drawbacks and is capable of jet dyeing polyamide fibers at 80 to 90°C. [Means for Solving the Problems] That is, the present invention provides a quality improver for polyamide fibers, which is characterized by comprising at least one compound represented by the following general formula. H [-NHC 3 H 6 O (-C 2 H 4 O)- o C 3 H 6 NHCO-A-
CO] -l OH (In the above formula, A is -C6H4- or ( -CH2 ) -n , where m is an integer of 2 to 8 , and n is 10 to 90
, l represents an integer from 1 to 10. ) The compounds of the formula of the present invention are diamines and dicarboxylic acids represented by the general formula H2NC3H6O ( -C2H4O ) -oC3H6NH2 (n=10-90), such as diamines and dicarboxylic acids, e.g. , terephthalic acid, dimethyl terephthalate, bis-β-hydroxyethyl terephthalate, bis-
It is obtained through a condensation reaction with aromatic carboxylic acids such as β-hydroxyterephthalate and phthalic acid, or fatty acid carboxylic acids such as succinic acid, adipic acid, sebacic acid, and citric acid.The reaction can be carried out using a conventional method. Bye. In carrying out the invention, the compound of the formula is added in an amount of 0.01 to 5%, preferably 0.05 to 5%, based on the polyamide fibers.
This can be done by using 1% owf and adding it to the processing bath. The compound of the formula not only exhibits an excellent anti-wrinkle effect, but also provides good flexibility and smoothness even in the bath, so it reduces the contact friction resistance between fabrics or between fabrics and machines (metals), and improves the quality of fibers. In order to protect the surface, it has the effect of preventing wrinkles as well as scratches and dents. On the other hand, it does not affect dyeing properties and does not cause a decrease in build-up. In addition, it has low foaming properties and good workability, so it can be used with a jet dyeing machine at 80%
This makes it possible to carry out dyeing processing at temperatures of ~90°C. EXAMPLES The invention will now be further explained by way of examples. Synthesis Example 1 71.4 parts of dipropylaminated compound of PEG #600 (0.1
mol) and bis-β-hydroxyethyl terephthalate (hereinafter abbreviated as BHET) 34.0 parts (0.125 mol)
was charged into a vacuum reaction vessel, replaced with N 2 -gas, and heated to 130
℃, reacted at 205℃±5℃ for 4 hours under reduced pressure (degree of vacuum: 10-20mmHg), and then cooled to complete the reaction (total amine value of the reactants).
HClO 4 method 8.1) and then 368 parts of warm water were added to completely dissolve the reaction product, and the pH was adjusted to 6.5 with acetic acid to obtain an invention product [1] with an effective concentration of 20%. The viscosity at 20℃ is
It was 56 c.p (B type viscometer). Synthesis Example 2 111.4 parts (0.1 mol) of dipropylaminated PEG #1000 and 34.0 parts (0.125 mol) of BHET were charged and reacted in the same manner as in Synthesis Example 1. The total amine value of the product was 5.3. A 20% aqueous solution was prepared in the same manner as in Example 1. The viscosity is
109c.p, and designated this as an invention [2]. Synthesis Example 3 Dipropylaminated compound of PEG #4000 1029 (0.25
mol) and 85 parts (0.3 mol) of BHET were reacted in the same manner as in Synthesis Example 1. The total amine value of the product was
It was 5.6. A 20% aqueous solution of this product was prepared as in Example 1. The viscosity was 93c.p, and this was designated as Invention Product [3]. Synthesis Example 4 111.4 parts (0.1 mol) of dipropylaminated PEG #1000 and 22.2 parts (0.11 mol) of sebacic acid were charged and reacted in the same manner as in Synthesis Example 1. The total amine value of the product was 4.8. . A 20% aqueous solution of this product was prepared as in Example 1. The viscosity was 46 c.p, and this was designated as the product of the present invention [4]. Synthesis Example 5 111.4 parts (0.1 mol) of dipropylaminated PEG #1000 and 16.1 parts (0.11 mol) of adipic acid were charged and reacted in the same manner as in Synthesis Example 1. The total amine value of the product was 3.7. . A 20% solution of this product was prepared as in Example 1. The viscosity was 112 c.p, and this was designated as the product of the present invention [5]. Invention products [1] to [5] obtained in this way
The effect of this product will be compared with that of a reference product in the following examples. Example 1 Minizette jet dyeing tester (manufactured by Texam Giken)
Nylon taffeta 180cm x 120
cm (vertical x horizontal) 140g to 5500ml water (bath ratio 1:
40: Add a bath ratio of 1:5 to 10 in the main body of the dyeing system, and a bath ratio of 1:40 when adding the dye solution in the liquid flow pump pipe,
Kayanol Mill.Blue GW 0.3% owf was used as the dye, and 2 g of quality improver was added to the bath for evaluation.
The dyeing temperature is increased from 20℃ at a rate of 2℃/min to 80℃×30
30 minutes at 90°C, then rapidly cooled, drained at 70°C, washed twice with water, dehydrated, and dried (75°C).
℃). The amount of foaming during dyeing, the occurrence of wrinkles on the dried fabric, and the build-up were visually observed and evaluated. Furthermore, the texture (flexibility) was also compared based on the tactile sensation.

【表】 実施例 2 実施例1に準じて、ナイロン/スパンデツク
ス/綿(リバーシブルニツト)をボイルで30分染
色した。その結果を下記に示す。
[Table] Example 2 According to Example 1, nylon/spandex/cotton (reversible knit) was dyed by boiling for 30 minutes. The results are shown below.

【表】 ※※ 比較品4:アルキルリン酸エステル系
以上のように、本発明品をポリアミド系繊維の
染色浴中に添加する事により、染色性の低下がな
く、防シワ、柔軟性、低起泡性に優れるため、液
流染色法にても高品位染色物を得る事が出来た。 実施例における評価基準 低起泡性 〇:起泡性殆んどなし △:染色機内空間の約1/2泡立つ ×:染色機内空間の殆んどが泡層と
なる 防シワ性 〇:殆んどシワの発生なし(ヒート
セツトにて消えるシワ) △:かなりシワの発生がある(一部
ヒートセツトにて消えるシ
ワ) ×:シワの発生多く、ヒートセツト
にても消えないシワが多い ビルドアツプ〇:ブランクと同等の染色濃度で
残染料なし △:やや濃度低下認められ、残染
料少し有り ×:残染料多い 風 合 〇:良好 △:比較的柔かい ×:粗硬
[Table] ※※ Comparative product 4: Alkyl phosphate ester system As described above, by adding the product of the present invention to the dyeing bath of polyamide fibers, there is no decrease in dyeability, wrinkle resistance, flexibility, and low Due to its excellent foaming properties, it was possible to obtain high-quality dyed products even by jet dyeing. Evaluation criteria in Examples Low foaming property 〇: Almost no foaming property △: About 1/2 of the space inside the dyeing machine foams ×: Most of the space inside the dyeing machine becomes a foam layer Wrinkle resistance 〇: Almost no foaming property No wrinkles (wrinkles that disappear with heat-setting) △: There are a lot of wrinkles (some wrinkles disappear with heat-setting) ×: Many wrinkles, many wrinkles that do not disappear even with heat-setting Build-up 〇: Blank and No residual dye at the same dye density △: A slight decrease in density, some residual dye ×: A lot of residual dye Texture 〇: Good △: Relatively soft ×: Rough and hard

Claims (1)

【特許請求の範囲】 1 下記一般式で示される化合物の少なくとも
1種からなることを特徴とするポリアミド系繊維
用浴中品質向上剤。 H〔−NHC3H6O(−C2H4O)−oC3H6NHCO−A−
CO〕−lOH (上式中、Aは−C6H4−又は(−CH2)−nであり、
ここでmは2〜8の整数であり、nは10〜90の整
数、lは1〜10の整数を表わす。)
[Scope of Claims] 1. An in-bath quality improver for polyamide fibers, characterized by comprising at least one compound represented by the following general formula. H [-NHC 3 H 6 O (-C 2 H 4 O)- o C 3 H 6 NHCO-A-
CO ] -l OH (in the above formula, A is -C6H4- or ( -CH2 ) -n ,
Here, m is an integer of 2 to 8, n is an integer of 10 to 90, and l is an integer of 1 to 10. )
JP60193199A 1985-09-03 1985-09-03 Quality enhancer in bath Granted JPS6253484A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60193199A JPS6253484A (en) 1985-09-03 1985-09-03 Quality enhancer in bath

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60193199A JPS6253484A (en) 1985-09-03 1985-09-03 Quality enhancer in bath

Publications (2)

Publication Number Publication Date
JPS6253484A JPS6253484A (en) 1987-03-09
JPS6312198B2 true JPS6312198B2 (en) 1988-03-17

Family

ID=16303949

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60193199A Granted JPS6253484A (en) 1985-09-03 1985-09-03 Quality enhancer in bath

Country Status (1)

Country Link
JP (1) JPS6253484A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0288276U (en) * 1988-12-27 1990-07-12

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0288276U (en) * 1988-12-27 1990-07-12

Also Published As

Publication number Publication date
JPS6253484A (en) 1987-03-09

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