JPS5966570A - Production of modified polyester fiber - Google Patents

Production of modified polyester fiber

Info

Publication number
JPS5966570A
JPS5966570A JP17251982A JP17251982A JPS5966570A JP S5966570 A JPS5966570 A JP S5966570A JP 17251982 A JP17251982 A JP 17251982A JP 17251982 A JP17251982 A JP 17251982A JP S5966570 A JPS5966570 A JP S5966570A
Authority
JP
Japan
Prior art keywords
fiber
polyester fibers
fibers
producing
modified
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
JP17251982A
Other languages
Japanese (ja)
Inventor
武居 庄治
倉田 建夫
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.)
Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo KK
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 Asahi Chemical Industry Co Ltd, Asahi Kasei Kogyo KK filed Critical Asahi Chemical Industry Co Ltd
Priority to JP17251982A priority Critical patent/JPS5966570A/en
Publication of JPS5966570A publication Critical patent/JPS5966570A/en
Pending legal-status Critical Current

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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、耐久性に優れた機能を有する改質ポリエステ
ル繊維の製法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing modified polyester fibers having excellent durability.

従来、ポリエステル繊維に制電、吸水、防汚、吸湿、換
水、撥油、抗ピル、防炎、難燃、防融、抗菌、防臭等の
機能を付与すること目的として、同#鼾イを種々の改質
加工剤(以下、「加工剤」という)で処理する方法が提
案されている。然しなから、これらの方法では、通常、
加工剤を繊維の比較的表面に付着させるに過ぎず、従っ
て、洗躍、ドライクリーニング等で加工剤の脱落が起こ
り、その耐久性に限界があった。
Conventionally, polyester fibers have been used for the purpose of imparting functions such as antistatic, water absorption, antifouling, moisture absorption, water exchange, oil repellency, anti-pill, flame retardant, flame retardant, anti-melting, antibacterial, and deodorizing properties. Methods of processing with various modification processing agents (hereinafter referred to as "processing agents") have been proposed. However, these methods usually
The processing agent is only attached to the relatively surface of the fibers, and therefore, the processing agent comes off during washing, dry cleaning, etc., and its durability is limited.

一方、繊維表面に重合性の加工剤を適用して、高分子量
の樹脂被膜を形成することによって水溶性および溶剤溶
解性を低下させて耐久性を向上させる技術も提案されて
いる。この様な技術では、繊維の風合変化が大きく、さ
らに洗ia等の揉布(もみ)効果による物理的摩擦によ
って、4Y4脂被膜、が剥離し易く、その耐久性には限
度があった。そのため柔軟な風合を維持し/ζ−ままで
、半永久的に改性機能ヶ付りすることができるポリエス
テル繊維の改質θlが必要であった。
On the other hand, a technique has also been proposed in which a polymerizable finishing agent is applied to the fiber surface to form a high molecular weight resin film, thereby reducing water solubility and solvent solubility and improving durability. With this technique, the texture of the fibers changes significantly, and the 4Y4 resin coating is likely to peel off due to physical friction caused by the rubbing effect of washing ia, and its durability is limited. Therefore, there is a need for a modification θl of polyester fiber that can semi-permanently add a modifying function while maintaining a soft feel/ζ-.

禾兇明の目的は、その様な従来技術め入点を橋11(シ
て、柔竺な風合、を有し2.洗濯などに対する耐久性に
優れた改i11? IJエステル繊オf(を提供するに
ある。
The purpose of the company was to improve upon such conventional technology by creating a new IJ ester fiber that has a soft texture, 2. has excellent durability against washing, etc. is to provide.

本発明に係る改Jj zl? IJエステル繊維の製法
は、ポリエステル繊維を改+p5加工剤で処理して改質
ポリエステ11石11.! X’i丁、をル・〕j枚す
るに際し、該ポリエステ川             
 ・ ル(A! #ffiとL7て、、 実’ls的恍ポリエ
チレンテレフタレート繊〆11よりなり、 > rf!
!] >IZ、周波数110Hzに闘る力学的(を1失
1[接(呻δ)?ピーク温度(T□8工)(℃)が10
5℃す+で、1−1つtanδ:のピーク値(い、δ)
maXが0,08以上であるイ′1°q造ン:有するポ
リエチレンプーリフタ1ノート11勺坏を用いることを
!1“ケ徴とする。
Modified Jj zl according to the present invention? The manufacturing method of IJ ester fiber is to process polyester fiber with modified + P5 processing agent to obtain modified polyester 11 stone 11. ! When making X'i Ding, the polyeste river
・ Le (A! #ffi and L7 are made of real polyethylene terephthalate fiber 11, > rf!
! ] >IZ, mechanically fighting against frequency 110Hz (1 loss 1 [Tangential (groaning δ)? Peak temperature (T
At 5°C, the peak value of 1-1 tan δ (i, δ)
A polyethylene pulley lifter with maX of 0.08 or more must be used. 1" symbol.

本発明で云う[ポリニス・アル繊維」とは、エチ1/ン
テレフタレート舎主繰返し単位として含む線状重合物で
、第三成分と17でイソフタル酸、スルホンfヒイソフ
タル酸のナトリウム塩、ポリエチレングリコールなどを
5距皇チ未満共重合せしめて、なるものを含む。また、
通當合成PR維に添加され、る艶消剤、安定剤、制電剤
などを含んでもよい。
[Polynis Al fiber] as used in the present invention is a linear polymer containing ethyl 1/n terephthalate as a main repeating unit, and the third component and 17 are isophthalic acid, sodium salt of sulfone hyisophthalic acid, polyethylene glycol, etc. Including those obtained by copolymerizing less than 50% of Also,
It may also contain matting agents, stabilizers, antistatic agents, etc., which are generally added to synthetic PR fibers.

′tだ71j:含塵一ついては通常のもVt維形成用の
範囲で・、やれば特に制限は、なり。
71j: The dust content is within the normal range for Vt fiber formation, so there are no particular restrictions.

1従来、ポリエチレンテレフターーi・よりなる衣オ(
用繊維は、紡速2.000 mA)J’l下で紡糸され
た未延伸繊維を3〜5倍に延伸してUO! )Zするの
が通常であった。このような延伸糸は、極めて強固な1
1111 無定形領域を有し・測定周波数110H″1ケけ6カ学
的損失正接(−δ)のピーク温度(Trr+ax )は
125〜135℃附近にあり、ツ>散染料て139℃1
11]近の高温下で染色され、染色後の’I”max 
%  ・125〜135℃1lfj近にある。
1 Conventionally, polyethylene telefter (i.
The fibers for this purpose are made by drawing the undrawn fibers spun at a spinning speed of 2.000 mA) 3 to 5 times to obtain UO! )Z was the norm. Such a drawn yarn has an extremely strong 1
1111 It has an amorphous region and the peak temperature (Trr+ax) of the measurement frequency 110H'' is around 125 to 135℃, and the peak temperature (Trr+ax) of the chemical loss tangent (-δ) is around 125 to 135℃.
11] 'I'max after dyeing, dyed under high temperature near
% ・125-135℃ Near 1lfj.

最近、紡糸工程のみで延伸せずにいわゆるPOYあるい
は高速紡糸繊維と呼ばれる繊訂(を?4Jる、省)月ヒ
を図って生産性を向上せしめた方法が徐々に採用されつ
つある。
Recently, a method called POY or high-speed spinning fiber, which improves productivity by reducing fiber production during the spinning process alone without drawing, is gradually being adopted.

POYと称するものは、はぼ3.’(1(10%’+)
程度の紡速で紡糸された繊維であって、延伸仮撚工程で
もって延伸と仮撚を同時に行ない、¥’j (IC糸を
Piるための原糸である。このようなPOYより得られ
た嵩高糸の(↑1rlδ)mいいは染色前後において0
.10附近、TrnaXは染色前後において120+−
130℃である。     ・ また、延伸仮撚工程を経ないPOYは(t11nδ)□
8が・10 、Tma。は90℃附近にあるが染色中に
3・Oq6を越える収ll′II′154<紮示し、染
色前後において30℃における初期モジュラスは′50
9/d未満であるりしかも引す」(弘! 1−if &
J、・2 、iid以下、伸度は80係以上あシ、衣刺
用摺糾としては実用に供されていない0       
 ・ 棟だ、高速紡糸繊#(+、ず万わち紡速か4.oo。
What is called POY is 3. '(1(10%'+)
It is a fiber that is spun at a spinning speed of about (↑1rlδ)m of bulky yarn is 0 before and after dyeing.
.. Around 10, TnaX is 120+- before and after staining
The temperature is 130°C.・ In addition, POY that does not go through the stretching false twisting process is (t11nδ) □
8 is 10, Tma. is around 90℃, but during dyeing, the yield exceeds 3.Oq6, and the initial modulus at 30℃ is
9/d or less.'' (Hiroshi! 1-if &
J, ・2, iid or less, elongation is 80 or more, not used for practical use as a suritsu for clothing 0
・ It's a ridge, high speed spinning fiber # (+, Zumanwachi spinning speed 4.oo.

ル勿〜8.00 、、Otn7分で紡糸され、延伸され
ていない繊維d2、(1+++1δ)mixがおおむね
0,10以上、Tm11Xが110〜115℃1i[」
近にちるが、100〜130℃で染色された後の(hn
 ?) )maxは0.08〜011で、Trr+nx
は115〜125℃になる。
8.00, Otn 7 minutes, undrawn fiber d2, (1+++1δ) mix approximately 0.10 or more, Tm11X 110-115℃1i[''
After being dyed at 100-130℃ (hn
? ))max is 0.08~011, Trr+nx
becomes 115-125°C.

すなわち染色中に熱水の作用に、し、)微細構造が変化
する。
That is, due to the action of hot water during dyeing, the microstructure changes.

4す1罪すれば、従来、ポリエステル繊維で、本発明に
云う如き、測定周波数11. OHzにおけるtanδ
のピーク温度Tmax (1:)が1059以丁で、」
」つt、lnδのピーク値(tanδ)m88が0.0
8以」二である+1゛ζ造特性を有し、衣ネ・1用繊紳
、として実用化されているものは存在しなかった。
To summarize, conventionally, with polyester fiber, the measurement frequency 11. tanδ at OHz
The peak temperature Tmax (1:) is 1059 or more,
'T, peak value of lnδ (tanδ) m88 is 0.0
There was no material that had +1゛ζ construction characteristics of 8 or more and had been put to practical use as a textile for clothing and clothing.

分散染料がポリエステル繊維に染着するのは、その無定
形領域である。無定形領域の構、i”il;を・表現す
、るtr’r性値として、上記TjIlaXと(tan
δ)mayの値が適切である。
It is in the amorphous region that the disperse dye dyes the polyester fiber. The above TjIlaX and (tan
The value of δ)may is appropriate.

TjnaXは通常ガラス転移温度、の約50℃高温に位
置し、(・tenδ)mnxは、温度T□8工に、おけ
る熱運動の活溌化した無定形領域内の分子鎖の月に関係
する・ 本発明において、TmAxおよび(しn JJ )rp
xは無定形領域内部の分子印のミクロブラウン:)5i
j動に原因、して発現する力学吸収(αA吸収)に関す
る値をχ′j味する。したがって、定性的には(鵬δ)
つ、が大きいほど無定形領域■が多く、Tmaxが低い
ほど無定形領域内の分子鎖のミクロブラウンj″!1価
すが低温で活溌化し、加工剤が吸着し易くなるO本発明
は、ポリエステルmv 屈内部へ加□工剤が浸透、拡散
1す乙現象は’Ct、1n l!l’)max及びTm
ax”’Th密iに関係し、弄りニス写ルi#II’<
イtの□測定周波級”11’0’J(zにおける幅δ)
max’l’)値が′02()8以1であり〈且つTm
azが105℃以乍であれば、加工剤の鉄層性がよく寸
だ嫂糸11内部への浸透性もよいとの知見にノリき完成
された。灯ましくはN Tmaxが80L′105℃で
あり、(tan a )mayがo、os〜05+ある
T jna In the present invention, TmAx and (Shin JJ)rp
x is the microbrown of the molecular mark inside the amorphous region:)5i
χ′j is the value related to mechanical absorption (αA absorption) caused by j motion. Therefore, qualitatively (Peng δ)
The larger Tmax is, the more amorphous regions ■ there are, and the lower Tmax is, the microbrown j''!monovalent molecules of the molecular chains in the amorphous regions become active at low temperatures, making it easier for processing agents to be adsorbed. The processing agent penetrates into the inside of polyester mv, and the diffusion phenomenon is 'Ct, 1n l!l') max and Tm
ax"'In relation to the secret I, tampering with the varnish copy #II'<
It's □Measurement frequency class"11'0'J (width δ at z)
max'l') value is '02()8 to 1, and Tm
The process was completed based on the knowledge that when az is 105° C. or higher, the processing agent has good iron layer properties and good penetration into the inside of the slit yarn 11. Preferably, N Tmax is 80L'105°C, and (tan a ) may be o, os~05+.

不発fjl]に用いられる茄工剤は二煎′□に、fil
J ’it臥吸水、防汚、1](湿、撥水、撥痛、:抗
ピル、防炎、′ff11F燃、防lAl1! 、抗1:
11防臭等の機能性を繊細に刊与す□るため用い上れて
いるものをいい、通常官能基を有する化合物からなる。
The eggplant agent used for unexploded fjl is
J'it is water absorbent, stain resistant, 1] (moisture, water repellent, pain repellent, anti-pill, flame retardant, ff11F fire, anti-Al1!, anti-1:
11. It refers to compounds that have been used to delicately provide functionality such as deodorization, and usually consists of a compound having a functional group.

かかる化谷物の分子量は2、50 (1以下で4)るこ
とが好ましい□′   □制電、吸水、防汚、””jk
Y(?’ltj 、親水性側力のための化合物としてQ
よ、y]?リエヂレングリコールとポリエチレンデレフ
タレニトとのブロック11月重合体1、Jl)リオキシ
エチレング□リコールジアクリレート、アクリル酸及び
メタアクリル酸めメトキシポリエチ1/ンクリコールエ
ステル、N−メチb−ルアクリル酸アミ□ド、メ夛クリ
ル酸、等が例示される。
The molecular weight of such chemical substances is preferably 2.50 (1 or less: 4) □′ □ Antistatic, water absorption, antifouling,
Y(?'ltj, Q as a compound for hydrophilic lateral forces
Yo, y]? Block polymer of polyethylene glycol and polyethylene derephthalenite 1, Jl) Lyoxyethylene glycol diacrylate, acrylic acid and methacrylic acid Methoxypolyethyl 1/n glycol ester, N-methyb- Examples include acrylic acid amide, methacrylic acid, and the like.

撥水、撥油性付与のた′めめ化合物としては、アルミニ
ウム石鹸、炭酸ジルうニウムアンモン、ア−1=)酢酸
ブチルエステル/ブチルチクネ−1−979化合物、ス
テアリン酸クロミッククロライド、ステアロイルメチル
アミドメチレンビリゾニウム塩等があシ、寸たポリアク
リル酸フッ化アルキルエステル等の有機フッ素化合物、
メチルノ・イrロジ・エン、ポリシロキサン等のシリコ
ン化合物等が例示される。
Examples of compounds for imparting water and oil repellency include aluminum soap, ammonium dicarbonate, a-1=)butyl acetate/butyl chicune-1-979 compound, stearic acid chromic chloride, and stearoylmethylamide methylene bicarbonate. Organic fluorine compounds such as rhizonium salts, fluorinated polyacrylic acid alkyl esters,
Examples include silicon compounds such as methyl-hydro-di-ene and polysiloxane.

防炎、難燃性付力のだめの化合物としては、リン含有化
合物、ノ・ロダン化合物、グーオ□尿素ホルマリン反応
物等がある。そのような化合物には、例えばトリスジブ
ロモプロピルホスフェート、テトラキスハイドロキシメ
チルホスホニウムクロライド、および次式で示される化
合物 以下余白 笠がある。
Examples of flame-retardant and flame-retardant imparting compounds include phosphorus-containing compounds, rhodan compounds, and urea-formalin reactants. Such compounds include, for example, tris dibromopropyl phosphate, tetrakis hydroxymethylphosphonium chloride, and compounds of the formula:

抗菌、防臭性側力のだめの化合物としては、第4級アン
モニウム化合物、有機水銀化合物、フェノール%jおよ
びその塩素化物、ナフ・テン酸等の有機酸の金属JMΦ
1がちり、そのような化合物の具体例としてeよ、N−
フルオロジ久ロロメチルチオフタルイミ・ド、N−ジメ
チルーN′−フ、壬ニル−N′−(フロロソクロロメチ
ルチオ)スルファミド、2−(4−チアゾイル)ベンズ
、イミダゾール、2−クロロ−2−(2,4−ノクロロ
フ、エノキシ)、ごエノール、クロールへキシジン、 ムクロライド等が例示される。
Examples of antibacterial and deodorizing compounds include quaternary ammonium compounds, organic mercury compounds, phenol and its chlorinated products, and organic acid metals such as naphthenic acid.
1, a specific example of such a compound is e, N-
Fluorodichloromethylthiophthalimide, N-dimethyl-N'-ph, Ibonyl-N'-(fluorosochloromethylthio)sulfamide, 2-(4-thiazoyl)benz, imidazole, 2-chloro-2-(2 , 4-nochloro, enoxy), enol, chlorhexidine, muchloride, etc.

加工剤として用いられる前記官能基を有する化合物の分
子量は2,500以下である。ことが好プしい。、分子
量がと、れより大きい場合は繊維内部への:吸着が少な
く、機能付与効果、が小さい。一方、、分子量が50〜
200程度の低分子化合物の場合でも重合性化合物であ
るときは、重合条件下で加工剤処理を行なうことによっ
て繊維内部での重合が。
The molecular weight of the compound having the functional group used as a processing agent is 2,500 or less. That's good. If the molecular weight is larger than that, there will be less adsorption into the interior of the fiber, and the effect of imparting functionality will be small. On the other hand, the molecular weight is 50~
Even in the case of a low molecular weight compound of about 200%, if it is a polymerizable compound, it can be polymerized inside the fiber by treating it with a processing agent under polymerization conditions.

可能となυ本発明の効果がイ↓Iられる。Possible effects of the present invention are shown below.

これら化合物の繊維への付着量は、001〜15m、!
襲であり・好ましくは0.5〜10重帰チである。0.
5重11%以下の場合yヒ合物によっては機能“側力効
果が低い場合があシ、また洗濯耐久性が劣る場合もある
。一方、表面への加工剤付着11が多 :くなって1′
5重伺チを超えると、風合変化が大きくなシ易い。
The amount of these compounds attached to the fibers is 001~15m!
・Preferably 0.5 to 10 times. 0.
When the weight is less than 5 weight and 11%, depending on the compound, the lateral force effect may be low, and the washing durability may be poor.On the other hand, the adhesion of finishing agents to the surface may be high 1′
When the thickness exceeds 5, the texture tends to change significantly.

これら化合物f’ 、j?リエステルー!に1ffli
用する場合、通常化合物の水溶液〜水系エマルジョンの
型態で・付与するでとが好ましい。また、−適用に際し
ては浸漬−加熱処理、浸漬−絞液−熱処理等公知の処理
方法をとることができるが、特に浸漬−加p′!(処理
が好ましい。
These compounds f', j? Riester! 1ffli to
When used, it is usually preferable to apply the compound in the form of an aqueous solution to an aqueous emulsion. In addition, - for application, known treatment methods such as immersion-heat treatment, immersion-squeezing-heat treatment, etc. can be used, but in particular immersion-ap'! (Treatment is preferred.

本発明の方法において、加工剤をポリエステル繊維に吸
着ぜしめA゛のち、180℃以上の乾熱処理を施すこと
により、沈痛耐久性が著しく向上する」騙合がある。
In the method of the present invention, by adsorbing the processing agent onto the polyester fibers and then subjecting them to dry heat treatment at 180° C. or higher, the sinking durability is significantly improved.

本2・1を明rC口う、しうな構造特性金有するポリエ
ステル繊糸11は、紡速4. (100m7分以上で紡
糸した未延伸、)?l)ニスデル繊維を、220℃乃至
300℃に加熱した乾熱31元気中址たは過熱水蒸気中
または両者の混合雰囲気中で熱処理することによシイノ
1られ、る。なお、この際、繊細にかかる張力は1 g
/d以下にする必ジンがある。かくして得られた71?
リエステル繊維は、そのま1の状態でも、常法により仮
撚加工した状態でも、または、紡績、原料としてのトつ
、ステープルファイバーにした状態でもそのf、j#造
特件は変らず、本発明の範囲に含まれる。
The polyester yarn 11 having the same structural characteristics as described in Book 2.1 has a spinning speed of 4. (Undrawn, spun for 100m or more for 7 minutes)? l) Nisdel fibers are heat-treated in a dry heat environment heated to 220° C. to 300° C., in superheated steam, or in a mixed atmosphere of both. In addition, at this time, the tension applied to the delicate part is 1 g.
There is a need to make it less than /d. 71 thus obtained?
Whether the polyester fiber is in its original state, false-twisted using conventional methods, spun, used as a raw material, or made into staple fiber, its f, j# manufacturing properties remain the same; within the scope of the invention.

、次に、本発明を構成するポリエチレンテレフタレート
繊維の力学的(Jj失正接(1捕δ)の測定法を示す。
Next, a method for measuring the mechanical loss tangent (Jj loss tangent (1 tangent δ)) of the polyethylene terephthalate fiber constituting the present invention will be described.

東洋ボールドウィン社製レオパイブロン(Rheo−v
jjr、、、on) DDV−11,c型動的粘弾性測
定装貨を用い、試料や、0,1m9、測定型波数IJ 
OHz、夕ず郵速度1.9ル分で乾燥空気中にて各温度
におけるーδ余測測定る。轡δ一温度曲線から一δのビ
ーク基環(Trr、x) (’C) 件、ピーク値[:
(1,Inδ)m−x)が得、られる。
Rheo-v manufactured by Toyo Baldwin
jjr,,,on) Using DDV-11, c type dynamic viscoelasticity measurement equipment, sample, 0.1 m9, measurement type wave number IJ
-δ measurements were taken at each temperature in dry air at OHZ and a postal speed of 1.9 l min.轡δ One temperature curve, one δ peak group ring (Trr, x) ('C), peak value [:
(1, Inδ) m−x) is obtained.

次に実施例をあげて本番r!IJをtt’+’ L <
畝、明する。
Next, I will give an example and let's see it in action! IJ to tt'+' L <
ridge, clear.

実施例1 紡速4. OOOm7r’J−で紡糸された7」?リエ
チレンテレ7タレート繊維’75 d/36 fを24
8℃の空気中70.85秒間、糸にかかる張力i 0.
03 、!9/aに規制して熱処理した。
Example 1 Spinning speed 4. 7” spun with OOOm7r’J-? Liethylene tele 7 tallate fiber '75 d/36 f 24
Tension applied to the thread i 0 for 70.85 seconds in air at 8°C.
03,! Heat treatment was carried out under a regulation of 9/a.

また、比り!文のだめ、紡速1.300 m/4;+で
紡糸後30℃で33倍に延伸した7 5 d/36 f
の繊維についても同様に熱処理した。
Also, compare! Bunnodame, 75 d/36 f drawn at 30°C to 33 times after spinning at a spinning speed of 1.300 m/4;+
The fibers were also heat treated in the same way.

得られた不発ツ]法繊維(Trnax : 101℃+
(tanδ)□38:0.210)および比較繊維CT
max : 145℃。
Obtained dud] method fiber (Trnax: 101℃+
(tan δ)□38:0.210) and comparative fiber CT
max: 145°C.

(tAnδ)rnaX=0125〕のそれぞれをトリコ
ット&H織に編立し、加工剤で処理した。加工剤処理と
しては、ポリエチレングリコール/刃?リエヂレンテレ
フタレートブロック共正合物(分芋量約600)を−3
0’j;//lの濃度に水に分散した液中に浸漬し、■
()0℃×60分処理し、続いて湯洗し、乾熱処理を2
00℃×40秒間行なった。
(tAnδ)rnaX=0125] were each knitted into a tricot & H weave and treated with a processing agent. As for processing agent treatment, polyethylene glycol/blade? -3
Immerse it in a solution dispersed in water to a concentration of 0'j;
( ) 0℃ x 60 minutes, followed by hot water washing and dry heat treatment for 2
The test was carried out at 00°C for 40 seconds.

イ5jられたそれぞれの編地の制電性、吸水性を第1表
に示し泥。本発明法の編地は4かめて高い耐洗(?ri
性を示した。     ′ 第1表 中1制市性:20℃X40%RHで測定。
Table 1 shows the antistatic properties and water absorption properties of each knitted fabric. The knitted fabric of the present invention has the highest wash resistance (?ri).
showed his sexuality. '1 in Table 1 Municipality: Measured at 20°C x 40%RH.

オネストメーター使用、印加電圧 s、ooov; ;iii;電−11,がV2tで減衰した時の時間−で
示した。        。
Using an honest meter, the applied voltage s, ooov; .

中2吸水性:26nllJの編地を蒸留水につけ、10
分間に吸い上げた水の高さで 表示した。
Medium 2 water absorption: Soak 26nllJ knitted fabric in distilled water,
It is expressed as the height of water sucked up per minute.

W:水洗沼回数 実施例2 加工剤処理として1.2− (4−チアシルベンズイミ
ダゾール)20重量%を含むグリコール酸を2097t
の濃度に分散した液中に浸漬した以外は、実施例1と同
様に加工剤処理を行ない、乾熱処理した。処理編地の抗
菌性を第2表に示しだ。
W: Number of times of washing Example 2 2097 tons of glycolic acid containing 20% by weight of 1.2-(4-thiacylbenzimidazole) was used as processing agent treatment.
The processing agent treatment and dry heat treatment were performed in the same manner as in Example 1, except that the specimens were immersed in a solution dispersed at a concentration of . Table 2 shows the antibacterial properties of the treated knitted fabrics.

第2表 *1△;編地表面に黒カビがわずかに認められる。Table 2 *1△; Black mold is slightly observed on the surface of the knitted fabric.

×:編地表面に黒カビが認められる。   □試験法:
 JIS−Z−2911(微抵抗試験)に準する。
×: Black mold is observed on the surface of the knitted fabric. □Test method:
Conforms to JIS-Z-2911 (microresistance test).

ツアペックドックス寒天培地に黒カビの食塩水懸濁液を
吹伺け、絹地を投入してj品度30℃で3日開放$((
i’)、 、絹地の周囲の黒カビの発育してない部分の
距離(ctn)を阻止帯として測定した。阻止帯が長い
程抗菌性が大きいことを示す。
Spray a saline suspension of black mold on a Czapek Dox agar medium, add silk and leave it open for 3 days at 30°C.
i'), The distance (ctn) of the area around the silk fabric where black mold did not grow was measured as the inhibition zone. The longer the inhibition zone, the greater the antibacterial properties.

実施例3 実施例1で得た紡速4.00 ny扮糸の熱処理系を、
仮撚ヒーター長0.8m、、スタビライズヒーター長0
.6mの2個のヒーターを有するU51撚加工機にて、
仮撚ヒーターの温IQ:1200℃、スタビライズヒー
ターの温度を1.90℃に設定し、スピンドルに詠糸条
を引用は撚数3.5・90t/m、延伸比1.1,25
 。
Example 3 The heat treatment system for the spinning speed 4.00 ny yarn obtained in Example 1 was
False twisting heater length 0.8m, Stabilizing heater length 0
.. Using a U51 twisting machine with two 6m heaters,
Temperature IQ of false twisting heater: 1200℃, stabilizing heater temperature set at 1.90℃, twisted yarn on spindle, number of twists: 3.5.90t/m, stretching ratio: 1.1.25
.

糸速146ル扮で仮撚加工した。False twisting was performed at a yarn speed of 146 ru.

また、比較のだめの実施例1でイ1)た紡速1.、30
0n1Δ〕糸の延伸糸を熱処理し、同様仮撚機にて、仮
撚ヒータ一温度220℃、スタビライズドヒータ一温度
200℃に設定し、スピンドルに該糸条を引掛は撚数3
.500 t/m’+延伸比0.985.糸速10 (
1ny’分で仮撚加工した7、得られた本発明法繊維お
よび比較繊維の加工糸全それぞれスムース編地に編立し
、常法にてイ、17練、染色し、続いてアンチフレーズ
に−19(開成fヒ学製難燃加工剤) 509/を濃度
の加工液へ浸漬し、絞液率85係で絞った後、200℃
で40秒間乾熱処理した。
In addition, the spinning speed 1.1) in Example 1 for comparison. , 30
0n1Δ]The drawn yarn of the yarn was heat-treated, and in the same false-twisting machine, the temperature of the false-twisting heater was set to 220°C and the temperature of the stabilized heater was set to 200°C, and the yarn was hooked on the spindle until the number of twists was 3.
.. 500 t/m'+stretch ratio 0.985. Yarn speed 10 (
False-twisted for 1 ny' minutes 7. All processed yarns of the obtained fibers of the present invention and comparison fibers were knitted into smooth knitted fabrics, kneaded for 17 minutes and dyed using the conventional method, and then knitted into antiphrases. -19 (flame retardant processing agent manufactured by Kaisei Fhigaku) 509/ was immersed in a processing solution with a concentration of 85%, and then heated to 200°C.
A dry heat treatment was performed for 40 seconds.

得られたそれぞれの織地の!゛(拍燃性能を第3表に示
した。いずれの編地もドライクリーニング後に′風合□
が変−て、ベトつかなくな・だが、本発明法の編地の耐
久性は良好であった。
of each fabric obtained! (The combustion performance is shown in Table 3. All knitted fabrics have a 'texture' after dry cleaning.
However, the durability of the knitted fabric produced by the method of the present invention was good.

第3表 傘lDCニドライクリーニング回数 難燃性: JIS−L−1091−71ミクロ・ぐ−チ
ー法で実施した。
Table 3: Number of Umbrella DC Ni Dry Cleaning Flame Retardancy: Conducted according to JIS-L-1091-71 Micro-Guchie method.

残炎時間秒は小さい方が、また、炭化面積←)″)は小
さい力が難燃性に優れている。
The smaller the afterflame time (seconds) and the smaller the carbonization area (←)″), the better the flame retardancy.

実施例4 7 x ) −/L/ /テトラクロロエタンのηの混
合溶婢:中でd111定せる35℃における固有粘度〔
η〕(以下〔η〕と表わす)が069のPETを紡糸湿
度302℃テ’fljl 0.35 mmφ、孔数24
の紡糸口金より紡出し、糸条に平行方向な22℃の冷t
al Jimで冷1:11固化させた後、油剤を1(f
1与し6,500m/分の速度で巻取った。得られた5
 0 d / 24 f (DI)gT織繊維、245
℃に加熱した空気中で0.85秒間、繊維に1″11け
る張力を31/d 、 1 、!9/d 。
Example 4 Mixed solution of 7
η] (hereinafter referred to as [η]) is 069, spun at a humidity of 302°C, 0.35 mmφ, and 24 holes.
Spun from a spinneret, cooled at 22°C parallel to the yarn.
After cooling and solidifying with Al Jim at 1:11, add oil to 1 (f
1 and was wound up at a speed of 6,500 m/min. obtained 5
0 d/24 f (DI)gT woven fiber, 245
The fibers were subjected to a tension of 31/d, 1,!9/d for 0.85 seconds in air heated to 1"11.

0、 :3.9 / dと変えて熱処理した。9れら茨
(処理した繊#1[及び床部■11すにIFの(−δ)
maxおよびT□8工を印、4衣に示しだ。
0, :3.9/d and heat-treated. 9. Thorns (treated fiber #1 [and floor part ■11 IF (-δ)
The max and T□8 are marked and shown on 4.

イIFられた4Laの繊維を実施例3と同様しζ鉄し理
し、これら矧燃力1ぼ編地の4!1を燃性能を第4表に
示した。
The IF-treated 4La fibers were treated with ζ iron in the same manner as in Example 3, and the flame performance of the 4!1 fabrics, which were knitted with a flame resistance of 1, was shown in Table 4.

Claims (1)

【特許請求の範囲】 1、 ポリエステル繊維を改質加工剤で処理して改質ポ
リエステル繊維全狙°(造するに際しミ該ポリエステル
繊維が、実質的にポリエチレンテレツクレートよシなシ
、測定周波数110Hzにおける力学的Jj1失jE接
(taδ)のピーク温度(”Trnax’ ) ’(℃
)が1()□5℃以下で、’i(′)−δのピーク値〔
(−δ扁工〕が0.08以上である構造特性を有′tふ
ことを特徴どする改’it 71? IJエステル繊維
の製法。   □2、ポリエステル繊維が、紡速4,0
00m/分以上で紡糸され、220〜300℃の温度範
囲内で0.1.9/d以下のtjjφ力下で熱処理せし
めたものである’I’M”lt’F jtloを求めi
)・i”12囲而]圧j記載の改1質ポリエステル繊鮪
の1Jiy法。 3、  シ+、(、、4i順hZ1:剤が、分子1i十
2’、 5’ OO以下であるJV41M求の範囲)l
、 J項6L:載の改質ポリエステル繊維の製法。
[Scope of Claims] 1. Polyester fibers are treated with a modifying agent to target all modified polyester fibers (when producing the polyester fibers, the polyester fibers are substantially not polyethylene telescrates), and the measurement frequency is 110 Hz. The peak temperature of the mechanical Jj1 loss jE tangent (taδ) ("Trnax') '(℃
) is below 1()□5℃, the peak value of 'i(')-δ [
71? A method for producing IJ ester fiber characterized by having a structural property of (-δ thickness) of 0.08 or more. □2.
Find 'I'M'lt'F jtlo, which is a material spun at a speed of 00 m/min or more and heat treated under a tjjφ force of 0.1.9/d or less within a temperature range of 220 to 300°C.
)・i”12 surroundings] 1Jiy method of modified 1st quality polyester fiber tuna described in pressure j. 3, shi +, (,, 4i order hZ1: JV41M where the agent has molecules 1i 12', 5' OO or less desired range)l
, Section J 6L: Method for producing modified polyester fibers.
JP17251982A 1982-10-02 1982-10-02 Production of modified polyester fiber Pending JPS5966570A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17251982A JPS5966570A (en) 1982-10-02 1982-10-02 Production of modified polyester fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17251982A JPS5966570A (en) 1982-10-02 1982-10-02 Production of modified polyester fiber

Publications (1)

Publication Number Publication Date
JPS5966570A true JPS5966570A (en) 1984-04-16

Family

ID=15943451

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17251982A Pending JPS5966570A (en) 1982-10-02 1982-10-02 Production of modified polyester fiber

Country Status (1)

Country Link
JP (1) JPS5966570A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62286742A (en) * 1986-06-05 1987-12-12 旭化成株式会社 Composite cloth-like substance
JPH01124678A (en) * 1987-11-09 1989-05-17 Asahi Chem Ind Co Ltd Polyester fiber and its production
CN106120329A (en) * 2016-06-30 2016-11-16 山东千榕家纺有限公司 A kind of antistatic, fire-retardant, the production technology of water and oil repellant anti-soil Multifunctional composite fabric

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62286742A (en) * 1986-06-05 1987-12-12 旭化成株式会社 Composite cloth-like substance
JPH01124678A (en) * 1987-11-09 1989-05-17 Asahi Chem Ind Co Ltd Polyester fiber and its production
JP2548242B2 (en) * 1987-11-09 1996-10-30 旭化成工業株式会社 Polyester fiber and method for producing the same
CN106120329A (en) * 2016-06-30 2016-11-16 山东千榕家纺有限公司 A kind of antistatic, fire-retardant, the production technology of water and oil repellant anti-soil Multifunctional composite fabric

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