JPS6411748B2 - - Google Patents

Info

Publication number
JPS6411748B2
JPS6411748B2 JP58014659A JP1465983A JPS6411748B2 JP S6411748 B2 JPS6411748 B2 JP S6411748B2 JP 58014659 A JP58014659 A JP 58014659A JP 1465983 A JP1465983 A JP 1465983A JP S6411748 B2 JPS6411748 B2 JP S6411748B2
Authority
JP
Japan
Prior art keywords
ptfe
fibers
flame
impregnated
aggregate
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
JP58014659A
Other languages
Japanese (ja)
Other versions
JPS59144679A (en
Inventor
Kozo Yamada
Takenobu Hasebe
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.)
Teijin Ltd
Original Assignee
Toho Rayon 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 Toho Rayon Co Ltd filed Critical Toho Rayon Co Ltd
Priority to JP58014659A priority Critical patent/JPS59144679A/en
Publication of JPS59144679A publication Critical patent/JPS59144679A/en
Publication of JPS6411748B2 publication Critical patent/JPS6411748B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

【発明の詳細な説明】 本発明は、ジオクチルコハク酸エステルスルホ
ン酸ソーダを特定量付着させた耐炎繊維又は炭素
繊維の集合体に関する。耐炎繊維又は炭素繊維
が、その耐薬品性、摺動性を利用し、パツキング
材として用いられることは知られている。このよ
うな繊維材料をパツキング材などとして使用する
場合、この繊維材料からなる紡績糸、織物、不織
布などにポリテトラフロロエチレン(PTFE)な
どのポリフロロエチレンを含浸させたものが用い
られている。また、前記繊維材料の紡績糸などを
組紐などに組成する場合に予めPTFEを含浸させ
ておくと、糸切れ等がなく編組を容易に行うこと
ができ、かつ緻密性、摺動性の優れた製品が得ら
れる。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an aggregate of flame-resistant fibers or carbon fibers to which a specific amount of sodium dioctylsuccinate sulfonate is attached. It is known that flame-resistant fibers or carbon fibers are used as packing materials by taking advantage of their chemical resistance and sliding properties. When such fibrous materials are used as packing materials, spun yarns, woven fabrics, nonwoven fabrics, etc. made of these fibrous materials are impregnated with polyfluoroethylene such as polytetrafluoroethylene (PTFE). In addition, when composing spun yarns of the above-mentioned fiber materials into braided cords, etc., impregnating them with PTFE in advance allows braiding to be easily performed without yarn breakage, etc., and has excellent denseness and sliding properties. product is obtained.

しかしながら、PTFEの含浸は通常その水性エ
マルジヨンを用いて行われるところ、耐炎繊維又
は炭素繊維は水性エマルジヨンとの親和性が悪
く、また、これら繊維の紡績糸には表面処理剤が
付着していることもあり、PTFEエマルジヨンを
これら繊維の集合体の内部まで充分に浸透させる
ことは困難であつた。本発明者等はこのような繊
維材料に対しPTFEエマルジヨンを充分浸透させ
てPTFEを有効に含浸させる技術について検討の
結果、下式(1)のジオクチルコハク酸エステルスル
ホン酸ソーダを予め付着させた耐炎繊維又は炭素
繊維の集合体にPTFEエマルジヨンを浸透させ、
次いで乾燥すると、耐炎繊維又は炭素繊維の集合
体にPTFEを有効に含浸できることを見出し、本
発明に至つたものである。
However, impregnation with PTFE is usually carried out using its aqueous emulsion, but flame-resistant fibers or carbon fibers have poor affinity with aqueous emulsions, and the spun yarns of these fibers have surface treatment agents attached to them. Therefore, it was difficult to sufficiently penetrate the PTFE emulsion into the inside of these fiber aggregates. The present inventors investigated a technique for effectively impregnating PTFE with a PTFE emulsion by sufficiently permeating such fiber materials. As a result, the present inventors found that a flame-retardant material with dioctyl succinate sodium sulfonate of the following formula (1) attached in advance was developed. Infiltrating the fiber or carbon fiber aggregate with PTFE emulsion,
The inventors have discovered that by drying the fibers, the flame-resistant fibers or carbon fiber aggregates can be effectively impregnated with PTFE, leading to the present invention.

すなわち、本発明は下記の通りである。 That is, the present invention is as follows.

(1) ジオクチルコハク酸エステルスルホン酸ソー
ダを0.1〜1%(owf)付着させた耐炎繊維又
は炭素繊維の集合体。
(1) An aggregate of flame-resistant fibers or carbon fibers to which 0.1 to 1% (OWF) of sodium dioctyl succinate sulfonate is attached.

ここにowfは対繊維重量の意味である。 Here, owf means fiber weight.

この付着ずみの耐炎繊維又は炭素繊維の集合体
に、ポリテトラフロロエチレンエマルジヨンを浸
透させ、次いで乾燥すると、集合体へのポリテト
ラフロロエチレンの含浸を有効に行うことがで
き、集合体に50%(owf)以上のPTFEを均一に
含浸させることができる。特に紡績糸等の集合体
にPTFEを含浸させる場合に、紡績糸等をPTFE
エマルジヨン浴中に通すだけで充分な量のPTFE
を含浸させることができる。
By impregnating the adhered aggregate of flame-resistant fibers or carbon fibers with a polytetrafluoroethylene emulsion and then drying, the aggregate can be effectively impregnated with polytetrafluoroethylene. % (owf) or more of PTFE can be impregnated uniformly. Especially when impregnating an aggregate of spun yarn, etc. with PTFE,
Enough amount of PTFE to pass through the emulsion bath
can be impregnated with.

本発明において、耐炎繊維又は炭素繊維とは、
アクリロニトリル系繊維、レーヨン繊維、ピツチ
系繊維、フエノール系繊維などの有機繊維を既知
の方法によつて耐炎処理又は引続き炭素化処理し
て得られるもので、通常用いられる意味での耐炎
繊維及び炭素繊維である。また、これら繊維の集
合体とは、これら繊維のストランド、不織布、紡
績糸、織物、組紐などである。特にアクリロニト
リル系繊維を酸化処理して得た耐炎繊維の紡績糸
は、強度も高く、このアクリロニトリル系耐炎繊
維のトウから紡績された太番手の紡績糸は、
PTFEの含浸性がよい。このPTFE含浸紡績糸
は、織物、組紐への極めて優れた加工性を有する
と同時に、パツキング材としてときに優れたシー
ル性と摺動性を発揮する。
In the present invention, flame-resistant fibers or carbon fibers are
It is obtained by subjecting organic fibers such as acrylonitrile fibers, rayon fibers, pitch fibers, and phenolic fibers to flame-resistant treatment or subsequent carbonization treatment using known methods, and is defined as flame-resistant fibers and carbon fibers in the commonly used sense. It is. In addition, the aggregate of these fibers includes a strand of these fibers, a nonwoven fabric, a spun yarn, a woven fabric, a braid, and the like. In particular, the spun yarn of flame-resistant fiber obtained by oxidizing acrylonitrile fiber has high strength, and the thick yarn spun from the tow of this flame-resistant acrylonitrile fiber has a high strength.
Good impregnation of PTFE. This PTFE-impregnated spun yarn has extremely excellent processability into fabrics and braids, and at the same time exhibits excellent sealing and sliding properties when used as a packing material.

ジオクチルコハク酸エステルスルホン酸ソーダ
は、前記式示した通りの化合物であり通常約70%
の水溶液で使用される。
Sodium dioctyl succinate sulfonate is a compound as shown in the above formula and is usually about 70%
used in aqueous solution.

この化合物を繊維集合体に0.1〜1%(owf)
付着させる。付着量が0.1%より少いと効果がな
く、逆に1%より多くなると、含浸したPTFEの
脱落が生じやすくなる。付着方法としては、通常
繊維に対し界面活性剤の付与と同一の方法が採用
される。すなわち、浸漬法、スプレー法、ローラ
ー接触法等がそれである。この付着処理に先だつ
て、繊維材料に付与されている界面活性剤(紡績
油剤)などの表面処理剤を水洗、有機溶剤洗浄な
どによつて除去しておくと、より好ましい結果を
与える。付着量の調整は、溶液濃度の調整、しぼ
り率の調整など通常の方法により行われる。付着
後80〜150℃にて乾燥される。
Add this compound to the fiber aggregate at 0.1-1% (owf)
Make it adhere. If the amount of adhesion is less than 0.1%, there will be no effect, and if it is more than 1%, the impregnated PTFE will easily fall off. As for the method of attachment, the same method used for applying surfactants to fibers is usually adopted. That is, immersion methods, spray methods, roller contact methods, etc. are examples. Prior to this adhesion treatment, if the surface treatment agent such as a surfactant (spinning oil) applied to the fiber material is removed by washing with water or organic solvent, more favorable results will be obtained. The amount of adhesion is adjusted by conventional methods such as adjusting the solution concentration and squeezing rate. After adhesion, it is dried at 80-150°C.

このようにして0.1〜1%(owf)のジオクチ
ルコハク酸エステルスルホン酸ソーダを付着され
た繊維材料は、好ましくは、PTFEエマルジヨン
と接触させ、繊維材料の集合体内部にPTFEエマ
ルジヨンを浸透させ、次いで乾燥付される。乾燥
は80〜150℃の温度にて通常の方法により行われ
る。
The fibrous material thus deposited with 0.1-1% (owf) of sodium dioctyl succinate sulfonate is preferably contacted with a PTFE emulsion to infiltrate the PTFE emulsion inside the mass of fibrous material, and then Dry. Drying is carried out in a conventional manner at a temperature of 80-150°C.

次に実施例により本発明を説明する。 Next, the present invention will be explained with reference to Examples.

実施例 1 (集合体の製造) アクリロニトリル系繊維を酸化処理して得られ
た耐炎繊維の紡績糸をジオクチルコハク酸エステ
ルスルホン酸ソーダ70%水溶液中に導入した後、
80℃にて乾燥し、紡績糸に前記化合物を0.7%
(owf)付着させた集合体を得た。
Example 1 (Manufacture of aggregate) After introducing a spun yarn of flame-resistant fiber obtained by oxidizing acrylonitrile fiber into a 70% aqueous solution of dioctyl succinate ester sodium sulfonate,
Dry at 80℃ and add 0.7% of the above compound to the spun yarn.
(owf) attached aggregates were obtained.

(集合体の使用) 次いで、この紡績糸をPTFE60%濃度のエマル
ジヨンに2秒間通し、ゴムローラーでスクイズ
し、140℃にて2.5時間乾燥した。得られた紡績糸
のPTFEの含浸量は62%(owf)であつた。
(Use of aggregate) Next, this spun yarn was passed through an emulsion containing 60% PTFE for 2 seconds, squeezed with a rubber roller, and dried at 140° C. for 2.5 hours. The amount of PTFE impregnated in the obtained spun yarn was 62% (owf).

比較のために前記化合物にて処理せず、直接
PTFEを含浸させた場合、PTFEの含浸量は40%
であつた。また、前記化合物に代え、オクチルフ
オスフエート、ポリエチレングリコールラウリル
エーテルを各々付与後同様にしてPTFEエマルジ
ヨン中を通し、PTFEを含浸させたところ、
PTFEの含浸量は夫々54%、52%であつた。
For comparison, the sample was prepared directly without treatment with the above compound.
When impregnated with PTFE, the amount of PTFE impregnated is 40%
It was hot. In addition, instead of the above compound, octyl phosphate and polyethylene glycol lauryl ether were applied and passed through a PTFE emulsion in the same manner to impregnate PTFE.
The amount of PTFE impregnated was 54% and 52%, respectively.

実施例 2 実施例1において用いた紡績糸を予め有機溶剤
(アルコール/ベンゼン混合液)中に70℃、3時
間浸漬した後、実施例1と同様にして集合体を得
た。
Example 2 The spun yarn used in Example 1 was previously immersed in an organic solvent (alcohol/benzene mixture) at 70°C for 3 hours, and then an aggregate was obtained in the same manner as in Example 1.

このものを使用して、前記と同様にして得られ
た紡績糸のPTFE含浸量は、79%であつた。
Using this material, the spun yarn obtained in the same manner as above had a PTFE impregnation amount of 79%.

比較のために、有機溶剤処理のみ行い、ジオク
チルコハク酸エステルスルホン酸ソーダの付与を
行わずにPTFEを含浸させたところ、PTFEの含
浸量は53%にとどまつた。
For comparison, when PTFE was impregnated with only organic solvent treatment and no addition of sodium dioctyl succinate sulfonate, the amount of PTFE impregnated remained at 53%.

Claims (1)

【特許請求の範囲】[Claims] 1 ジオクチルコハク酸エステルスルホン酸ソー
ダを0.1〜1%(owf)付着させた耐炎繊維又は
炭素繊維の集合体。
1 An aggregate of flame-resistant fibers or carbon fibers to which 0.1 to 1% (owf) of dioctyl succinate sulfonic acid sodium is attached.
JP58014659A 1983-02-02 1983-02-02 Flame resistant fiber and impregnation thereof Granted JPS59144679A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58014659A JPS59144679A (en) 1983-02-02 1983-02-02 Flame resistant fiber and impregnation thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58014659A JPS59144679A (en) 1983-02-02 1983-02-02 Flame resistant fiber and impregnation thereof

Publications (2)

Publication Number Publication Date
JPS59144679A JPS59144679A (en) 1984-08-18
JPS6411748B2 true JPS6411748B2 (en) 1989-02-27

Family

ID=11867335

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58014659A Granted JPS59144679A (en) 1983-02-02 1983-02-02 Flame resistant fiber and impregnation thereof

Country Status (1)

Country Link
JP (1) JPS59144679A (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4994303A (en) * 1988-03-21 1991-02-19 Garlock, Inc. Fiber impregnation process
GB9506715D0 (en) * 1995-03-31 1995-05-24 Solatrim Ltd Improved additive
JP4074820B2 (en) * 2003-02-19 2008-04-16 東邦テナックス株式会社 Polyacrylonitrile-based oxidized fiber spun yarn
CN114901903A (en) 2020-01-22 2022-08-12 东丽株式会社 Carbon fiber bundle coated with sizing agent and method for producing same
JP6745556B1 (en) * 2020-02-06 2020-08-26 竹本油脂株式会社 Treatment agent, flame-retardant fiber non-woven fabric, carbon fiber non-woven fabric, and methods for producing the same
JP6795228B1 (en) * 2020-02-06 2020-12-02 竹本油脂株式会社 Treatment agents, flame-resistant non-woven fabrics, carbon fiber non-woven fabrics, and their manufacturing methods

Also Published As

Publication number Publication date
JPS59144679A (en) 1984-08-18

Similar Documents

Publication Publication Date Title
DE752782C (en) Process for the production of wool substitute fibers from synthetic linear high polymers, in particular polyamides, by crimping
DE1942742C3 (en) Process for improving the dyeability of hydroxyl-containing polymers of textile character
US2381863A (en) Method of fungusproofing textiles
DE762964C (en) Process for making cellulose fibers water repellent
JPS6350462B2 (en)
US2495233A (en) Method of treating cellulosic materials with trimethylolphenol
JPS6411748B2 (en)
DE1795688B2 (en) Process for the production of fluorine-containing polymers. Elimination from: 1468833
US3971093A (en) Mop having a washing resistance
DE3336584A1 (en) METHOD FOR PRODUCING CARBON FIBERS OR GRAFIT FIBERS
DE2922809A1 (en) LARGE SHRINKAGE ACRYLIC FIBERS AND THE METHOD OF MANUFACTURING THEM
CH543631A (en) Fluoroglycidyl ethers for treating textiles and other
US2036424A (en) Impregnation of cotton materials
IE44896B1 (en) Process for the production of hygroscopic fibres and filaments if synthetic polymers
US2342746A (en) Process for making pile fabric
KR101503367B1 (en) Method of manufacturing yarn with water-repellency
US3617355A (en) Method of applying water and oil repellent finish for synthetic fibrous materials
DE3304351A1 (en) FLUOROCARBON MATERIAL AND THEIR USE
DE2827804A1 (en) USE OF MODIFIED CELLULOSEHYDRATE FIBERS FOR TIED FIBER FABRICS
US1958821A (en) Method of making artificial leather
WO2000066820A1 (en) Method for reducing the fibrillation tendency of cellulose fibres spun from solvents
DE2064901B2 (en) Homo or copolymers of 1,4 bis (heptafluonsopropoxy) 2,3 epoxybutane excreted from 2059013
DE2739179A1 (en) Metallising synthetic polymer esp. acrylonitrile! fibre - by depositing metal on fibre of high porosity
AT363168B (en) METHOD FOR PRODUCING HYDROPHILIC FIBERS OR FIBERS FROM AN ACRYLNITRILE HOMO OR COPOLYMER
US2864662A (en) Bleaching method