JP2000328452A - Production of heat-resistant polyamide-based fiber - Google Patents

Production of heat-resistant polyamide-based fiber

Info

Publication number
JP2000328452A
JP2000328452A JP14059299A JP14059299A JP2000328452A JP 2000328452 A JP2000328452 A JP 2000328452A JP 14059299 A JP14059299 A JP 14059299A JP 14059299 A JP14059299 A JP 14059299A JP 2000328452 A JP2000328452 A JP 2000328452A
Authority
JP
Japan
Prior art keywords
antioxidant
heat
polyamide
polyamide fiber
spinning
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
Application number
JP14059299A
Other languages
Japanese (ja)
Inventor
Toru Okada
徹 岡田
Seiichi Ochi
清一 越智
Yukio Okamoto
幸男 岡本
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.)
Toyobo Co Ltd
Original Assignee
Toyobo 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 Toyobo Co Ltd filed Critical Toyobo Co Ltd
Priority to JP14059299A priority Critical patent/JP2000328452A/en
Publication of JP2000328452A publication Critical patent/JP2000328452A/en
Pending legal-status Critical Current

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  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Chemical Treatment Of Fibers During Manufacturing Processes (AREA)

Abstract

PROBLEM TO BE SOLVED: To efficiently produce polyamide-based fibers excellent in heat resistance and further level dyeing properties. SOLUTION: An antioxidant is contained in a spinning oil when carrying out the melt spinning of polyamide-based fibers and applying the spinning oil to the resultant undrawn yarn prior to the winding thereof. In this case, the antioxidant is a semicarbazide-based compound represented by the general formula. formula: (CH3)2NNHCONH-(CH2)m-NHCONHN(CH3)2 (m denotes an integer of 1-11).

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する分野】本発明は耐熱性に優れ、染色品の
品位を向上することができるポリアミド系繊維の製造方
法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a polyamide fiber which has excellent heat resistance and can improve the quality of a dyed product.

【0002】[0002]

【従来の技術】ポリアミド系繊維は種々の優れた特性を
有するので、織編物等の布帛として広く利用されてい
る。ポリアミド系繊維製品では染色加工前に布帛形態を
安定化するために、130℃〜210℃の温度で30秒
〜3分間の乾熱処理が行われている。しかし、この熱処
理によって染色斑および染色筋が発生する問題が生じ易
い。つまり、熱処理のバラツキにより、染色性が低下し
たり、染色斑や染色筋が発生する。
2. Description of the Related Art Polyamide fibers have various excellent properties and are therefore widely used as woven or knitted fabrics. In the case of polyamide-based fiber products, dry heat treatment is performed at a temperature of 130 ° C to 210 ° C for 30 seconds to 3 minutes in order to stabilize the fabric form before dyeing. However, this heat treatment tends to cause a problem that stained spots and stained streaks are generated. That is, due to the variation in the heat treatment, the staining property is reduced, and stained spots and stained lines are generated.

【0003】これは、ポリアミド系繊維製品の布帛形態
安定化の為の熱処理により、ポリアミド系繊維のアミノ
末端基が減少して、酸性染料が染着されにくくなる為と
思われる。つまり、Ties Karstensらの報文Makromol.C
hem.No.191(1990)に掲載されているように、ポリアミド
分子中のアミノ末端基が高温加熱によって減少すること
やポリマー主鎖中のアミド結合が切断されアルデヒドお
よびケトンカルボニル基が生成し、これがアミノ基と反
応し黄色の色原体を形成することが知られている。前記
の熱によるアミノ末端基の減少および熱黄変はともにア
ミノ末端基が消費され、酸性染料の染着座席の減少を生
じ、結果として染色性が低下する。
This is presumably because the heat treatment for stabilizing the fabric form of the polyamide fiber product reduces the amino terminal groups of the polyamide fiber and makes it difficult for the acid dye to be dyed. In other words, the report Makromol.C of Ties Karstens et al.
As described in hem. No. 191 (1990), the amino terminal group in the polyamide molecule is reduced by heating at a high temperature, the amide bond in the polymer main chain is cleaved, and aldehyde and ketone carbonyl groups are generated, It is known that this reacts with an amino group to form a yellow chromogen. Both the heat-induced reduction of the amino terminal groups and the heat yellowing consume the amino terminal groups, resulting in a reduction in the number of dyeing sites for the acid dyes and consequently the dyeability is reduced.

【0004】かかる熱酸化劣化によるポリアミド系繊維
のアミノ末端基の減少や黄変を防ぐ方法として、通常の
ヒンダードフェノール系もしくは、ヒンダードアミン
系、セミカルバジド系化合物等の酸化防止剤を、重合時
もしくは染色加工段階(特に高温乾熱処理前)で添加す
る方法が知られているが、これらの方法であればアミノ
末端基の減少を抑え、黄変を防ぎ、結果として染色性向
上に有効であるが、前者の重合時添加方法では、原糸自
身が着色したり、最終製品で残存する酸化防止剤に起因
する各種黄変トラブル、例えば、NOxガス、プロパン
燃焼ガス等のガス黄変や光、熱での酸化防止剤自身の黄
変が問題となる場合があり、後者の染色加工段階で添加
する方法では、後加工工程が増えて効率的生産には不向
きである等の問題があった。
As a method for preventing the reduction or yellowing of the amino terminal group of the polyamide fiber due to the thermal oxidation deterioration, a conventional antioxidant such as a hindered phenol-based, hindered amine-based or semicarbazide-based compound is used during polymerization or dyeing. Methods of adding at the processing stage (especially before high-temperature dry heat treatment) are known, but these methods are effective in suppressing the decrease in amino terminal groups, preventing yellowing, and as a result, improving dyeability. In the former addition method at the time of polymerization, the yarn itself is colored or various yellowing troubles caused by the antioxidant remaining in the final product, for example, gas yellowing such as NOx gas, propane combustion gas, light, heat, etc. The yellowing of the antioxidant itself may be a problem, and the latter method of adding at the dyeing stage has a problem that the number of post-processing steps increases and is not suitable for efficient production. Was Tsu.

【0005】また、熱黄変を防ぐ方法として、熱処理温
度を下げたり、処理時間を短くする方法があるが、これ
らの方法は染色性向上には有効であるが、ポリアミド系
繊維製品の染色時の端部の丸まりやロープマークと呼ば
れる皺ができる等、布帛形態の安定性が悪くなり、染色
性と布帛形態安定性両方を満足するものはいまだ得られ
ていない。
As a method for preventing thermal yellowing, there are methods of lowering the heat treatment temperature and shortening the treatment time. These methods are effective for improving the dyeing property, but they are not effective for dyeing polyamide fiber products. , The stability of the fabric form is deteriorated, such as rounding of the ends and wrinkles called rope marks, and there is still no product that satisfies both the dyeability and the fabric form stability.

【0006】[0006]

【発明が解決しようとする課題】本発明は、耐熱性に優
れ、また均染性に優れたポリアミド系繊維を効率的に製
造する方法を提供することを目的とする。
SUMMARY OF THE INVENTION An object of the present invention is to provide a method for efficiently producing a polyamide fiber having excellent heat resistance and excellent levelness.

【0007】[0007]

【課題を解決するための手段】本発明は、ポリアミド系
繊維を溶融紡糸し、未延伸糸を捲き取る以前に紡糸油剤
を付与するに際し、紡糸油剤中に酸化防止剤を含有させ
ることを特徴とする耐熱性ポリアミド系繊維の製造方法
である。また、酸化防止剤が一般式(I)で示されるセミ
カルバジド系化合物である耐熱性ポリアミド系繊維の製
造方法である。 (CH3)2NNHCONH-(CH2)m-NHCONHN(CH3)2 (I) [式中mは1〜11の整数である。]
The present invention is characterized in that an antioxidant is contained in a spinning oil agent when a polyamide fiber is melt-spun and a spinning oil agent is applied before winding an undrawn yarn. This is a method for producing a heat-resistant polyamide fiber. Further, the present invention relates to a method for producing a heat-resistant polyamide fiber in which the antioxidant is a semicarbazide compound represented by the general formula (I). (CH 3 ) 2 NNHCONH- (CH 2 ) m-NHCONHN (CH 3 ) 2 (I) wherein m is an integer of 1 to 11. ]

【0008】以下に、本発明を詳細に説明する。本発明
におけるポリアミド系繊維とは、ナイロン−6、ナイロ
ン−6,6、ナイロン−4,6およびポリアミド/ポリ
エステル複合繊維等の合成繊維であり、好ましくはナイ
ロン−6を用いることができる。また、紡糸方法として
は、通常の溶融方式が適用される。また、ポリアミドポ
リマーは、通常添加される添加剤、例えば艶消剤、安定
剤、制電剤等を含んでいてもよい。繊維の断面形状およ
び繊度は用途に応じて適宜選択される。
Hereinafter, the present invention will be described in detail. The polyamide fibers in the present invention are synthetic fibers such as nylon-6, nylon-6,6, nylon-4,6 and polyamide / polyester conjugate fiber, and nylon-6 can be preferably used. As a spinning method, an ordinary melting method is applied. Further, the polyamide polymer may contain additives usually added, for example, a matting agent, a stabilizer, an antistatic agent and the like. The cross-sectional shape and fineness of the fiber are appropriately selected depending on the application.

【0009】本発明における紡糸油剤とは、合成繊維を
製造する際に通常使用されるもであり、鉱物油系、特殊
アニオン系、特殊ノニオン系、特殊カチオン系を用いる
ことができ、用途に応じて適宜選択される。
[0009] The spinning oil agent in the present invention is commonly used in the production of synthetic fibers. Mineral oils, special anions, special nonions, and special cations can be used. Selected as appropriate.

【0010】本発明における酸化防止剤とは、次式で示
されるセミカルバジド系化合物である。セミカルバジド
系化合物としては限定されるものではないが、例えば下
記一般式(I): (CH3)2NNHCONH-(CH2)m-NHCONHN(CH3)2 (I) [式中mは1〜11の整数である。]で示され、この中
で好ましいものとしては、m=6の化合物等があげられ
る。
The antioxidant in the present invention is a semicarbazide compound represented by the following formula. Although the semicarbazide compound is not limited, for example, the following general formula (I): (CH 3 ) 2 NNHCONH- (CH 2 ) m-NHCONHN (CH 3 ) 2 (I) It is an integer of 11. Among them, preferred are compounds having m = 6.

【0011】かかる酸化防止剤の付与量は該繊維に対し
て、0.001〜5重量%の範囲の中から選択される。
付与量がこの範囲内であれば、原糸着色もなく、また、
経済的に耐熱性の良好なものが得られる。
The amount of the antioxidant to be applied is selected from the range of 0.001 to 5% by weight based on the weight of the fiber.
As long as the applied amount is within this range, there is no coloring of the yarn,
Good heat resistance can be obtained economically.

【0012】具体的な付与方法としては、通常の溶融紡
糸をする際に、紡糸油剤中に酸化防止剤を添加しておい
てポリアミド系繊維に付与する。一般には該酸化防止剤
と紡糸油剤の水溶液あるいは水分散液を通常の油剤付与
装置で付与する。
As a specific method of application, an antioxidant is added to the spinning oil during ordinary melt spinning, and the solution is applied to the polyamide fiber. In general, an aqueous solution or aqueous dispersion of the antioxidant and the spinning oil is applied by a usual oil applying device.

【0013】[0013]

【実施例】以下に、本発明の耐熱性ポリアミド系繊維の
製造方法に関する具体例を詳細に説明するが、本発明は
実施例のみに限定されるものではない。実施例における
評価は次の評価方法によった。
EXAMPLES Hereinafter, specific examples relating to the method for producing the heat-resistant polyamide fiber of the present invention will be described in detail, but the present invention is not limited to only the examples. The evaluation in the examples was based on the following evaluation method.

【0014】(1)耐熱性 後述する実施例、比較例のように乾熱処理まで実施した
サンプルの黄変度を目視判定で3段階評価する。 ○;ほとんど黄変しない。 △;やや黄変する。 ×;かなり黄変する。
(1) Heat Resistance The degree of yellowing of a sample subjected to dry heat treatment as in Examples and Comparative Examples to be described later is evaluated by visual evaluation in three stages. ;: Almost no yellowing. Δ: slightly yellowed. X: considerably yellowed.

【0015】(2)染色性 後述する実施例、比較例のように乾熱処理まで実施した
サンプルをミーリングタイプ・ブルー系酸性染料(品
名:Kayanol Mill. Turq. Blue 3G 1%owf、日本化薬社
製)で98℃×30分酸性染色した後、染色性を目視判
定する。 ○;均一に染まる。 △;やや淡染部分がある。 ×;多数の淡染部分がある。
(2) Dyeing properties Samples which were subjected to dry heat treatment as in Examples and Comparative Examples described later were milled blue acid dyes (product name: Kayanol Mill. Turq. Blue 3G 1% owf, Nippon Kayaku Co., Ltd.) ) At 98 ° C for 30 minutes, and then the dyeability is visually determined. ;: Uniform dyeing. Δ: There is a slightly lightly dyed portion. X: There are many lightly dyed portions.

【0016】(3)寸法安定性 後述する実施例、比較例のように乾熱処理まで実施した
サンプルに10cmの印をつけて、98℃、30分の沸
水処理後の収縮率から評価する。 ○;ほとんど収縮しない。 △;やや収縮する。 ×;かなり収縮する。
(3) Dimensional stability Samples which have been subjected to dry heat treatment as in Examples and Comparative Examples to be described later are marked with a 10 cm mark, and evaluated from the shrinkage after a 98 ° C., 30 minute boiling water treatment. ;: Almost no shrinkage. Δ: Shrinks slightly. X; considerably shrinks.

【0017】実施例1 ナイロン−6レジンを通常の溶融紡糸装置を使用して、
溶融紡糸後、未延伸糸に下記式で示す化合物(a)のセ
ミカルバジド系化合物を紡糸油剤(主成分が鉱物油、特
殊アニオン系油剤)に対して3重量%添加して、該紡糸
油剤を繊維に対して1重量%を付与し、さらに延伸、熱
処理後捲き取った。得られた70デニール24フィラメ
ントのポリアミド繊維を経糸および緯糸に用いて、経糸
密度297本/インチ、緯糸密度110本/インチのタ
フタ織物を製織した。この織物を常法により精練後、1
95℃×3分の乾熱処理を実施した。得られた布帛の黄
変度、染色性、寸法安定性は表1のようになり、染色
性、寸法安定性ともに良好なものであった。
Example 1 Nylon-6 resin was prepared using a conventional melt spinning apparatus.
After the melt spinning, a semicarbazide compound represented by the following formula (a) is added to the undrawn yarn at 3% by weight with respect to the spinning oil (main component is mineral oil, special anion oil). And stretched and heat-treated. Using the obtained 70-denier 24-filament polyamide fiber for the warp and the weft, a taffeta fabric having a warp density of 297 yarns / inch and a weft yarn density of 110 yarns / inch was woven. After scouring the woven fabric by a conventional method,
A dry heat treatment was performed at 95 ° C. for 3 minutes. The yellowing degree, dyeability and dimensional stability of the obtained fabric were as shown in Table 1, and both the dyeability and the dimensional stability were good.

【0018】 (CH3)2NNHCONH-(CH2)6-NHCONHN(CH3)2 (a)(CH 3 ) 2 NNHCONH- (CH 2 ) 6 -NHCONHN (CH 3 ) 2 (a)

【0019】比較例1 紡糸油剤に酸化防止剤を添加しない以外は実施例1と同
様に糸を製造し、布帛を製織し、精練、熱処理を行っ
た。得られた布帛の黄変度、染色性、寸法安定性は表1
のようになり、寸法安定性は良好であったが、染色性は
品位に欠けるものであった。
Comparative Example 1 A yarn was produced in the same manner as in Example 1 except that an antioxidant was not added to the spinning oil, a fabric was woven, scoured and heat-treated. Table 1 shows the yellowing degree, dyeability and dimensional stability of the obtained fabric.
And the dimensional stability was good, but the dyeability was poor.

【0020】比較例2 酸化防止剤を付与しない以外は実施例1と同様に糸を製
造し、布帛を製織した。この織物を常法により精練後、
180℃×1分の熱処理を実施した。得られた布帛の黄
変度、染色性、寸法安定性は表1のようになり、染色性
は良好であったが、寸法安定性は品位に欠けるものであ
った。
Comparative Example 2 A yarn was produced and a fabric was woven in the same manner as in Example 1 except that no antioxidant was added. After scouring this woven fabric by the usual method,
Heat treatment was performed at 180 ° C. for 1 minute. The yellowing degree, dyeability and dimensional stability of the obtained fabric were as shown in Table 1. The dyeability was good, but the dimensional stability was poor in quality.

【0021】[0021]

【表1】 [Table 1]

【0022】[0022]

【発明の効果】本発明により、耐熱性に優れ、また均染
性に優れたポリアミド系繊維を効率的に製造することが
できる。
According to the present invention, polyamide fibers having excellent heat resistance and excellent levelness can be efficiently produced.

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4L033 AA08 AB01 AC05 AC15 BA01 BA78 4L038 AA22 BA17 BB07 DA12 DA20 ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4L033 AA08 AB01 AC05 AC15 BA01 BA78 4L038 AA22 BA17 BB07 DA12 DA20

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 ポリアミド系繊維を溶融紡糸し、未延伸
糸を捲き取る以前に紡糸油剤を付与するに際し、紡糸油
剤中に酸化防止剤を含有させることを特徴とする耐熱性
ポリアミド系繊維の製造方法。
1. A heat-resistant polyamide fiber produced by melt-spinning a polyamide fiber and adding an antioxidant to the spinning oil agent before the undrawn yarn is wound up. Method.
【請求項2】 酸化防止剤が一般式(I)で示されるセミ
カルバジド系化合物である請求項1記載の耐熱性ポリア
ミド系繊維の製造方法。 (CH3)2NNHCONH-(CH2)m-NHCONHN(CH3)2 (I) [式中mは1〜11の整数である。]
2. The method for producing a heat-resistant polyamide fiber according to claim 1, wherein the antioxidant is a semicarbazide compound represented by the general formula (I). (CH 3 ) 2 NNHCONH- (CH 2 ) m-NHCONHN (CH 3 ) 2 (I) wherein m is an integer of 1 to 11. ]
JP14059299A 1999-05-20 1999-05-20 Production of heat-resistant polyamide-based fiber Pending JP2000328452A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14059299A JP2000328452A (en) 1999-05-20 1999-05-20 Production of heat-resistant polyamide-based fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14059299A JP2000328452A (en) 1999-05-20 1999-05-20 Production of heat-resistant polyamide-based fiber

Publications (1)

Publication Number Publication Date
JP2000328452A true JP2000328452A (en) 2000-11-28

Family

ID=15272285

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14059299A Pending JP2000328452A (en) 1999-05-20 1999-05-20 Production of heat-resistant polyamide-based fiber

Country Status (1)

Country Link
JP (1) JP2000328452A (en)

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