JPH0657909B2 - Method for manufacturing fibrillated fabric - Google Patents
Method for manufacturing fibrillated fabricInfo
- Publication number
- JPH0657909B2 JPH0657909B2 JP60073338A JP7333885A JPH0657909B2 JP H0657909 B2 JPH0657909 B2 JP H0657909B2 JP 60073338 A JP60073338 A JP 60073338A JP 7333885 A JP7333885 A JP 7333885A JP H0657909 B2 JPH0657909 B2 JP H0657909B2
- Authority
- JP
- Japan
- Prior art keywords
- fabric
- benzoic acid
- polyamide
- fibrillated
- polyester
- 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
Links
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- Chemical Or Physical Treatment Of Fibers (AREA)
Description
【発明の詳細な説明】 本発明は、天然繊維に似たソフト感を有する風合及び表
面外観を与え、且つ布帛にコンパクト感を持たせた緻密
なフイブリル化布帛を提供せる布帛の製造法に関する。Description: TECHNICAL FIELD The present invention relates to a method for producing a fabric which gives a texture and a surface appearance having a soft feeling similar to that of natural fiber, and can provide a dense fibrillated cloth having a compact feeling. .
従来、合成繊維、例えばポリエステル、ポリアミドのフ
イラメントからなる布帛物は、その単糸維度が太いこと
や横断面形状が単純であるためにシルク、綿、麻等の天
然繊維に比較して風合、光沢が単調であり、プラスチツ
ク的なために冷たく感じ品位の低いものであつた。Conventionally, a synthetic fiber, for example, a fabric made of a filament of polyester, has a feeling that it is larger than a natural fiber such as silk, cotton, or hemp because of its large single yarn fiber and simple cross-sectional shape. The gloss was monotonous, and because it was plastic, it felt cold and of poor quality.
最近これら欠点を改良するために繊維横断面の異形化、
巻縮加工、複合繊維等が種々試みられているが、いまだ
に十分には目的を達成していない。近年合成繊維のフイ
ブリル化技術の進歩によりフイブリル化繊維で構成され
た布帛も可能となつた。そのひとつの技術として特公昭
53-35633号公報や特公昭56-16231号公報
等に例を見るが、その具体例としてポリアミドとポリエ
ステルからなる複合型ポリエステルフイラメントをポリ
アミドに対し膨潤能を有するベンジルアルコール等の処
理によりフイブリル化する方法等があるが、実施に当り
次の如き問題点があり、操業上制約があるのが実状であ
る。Recently, in order to improve these drawbacks, the cross-section of the fiber is modified,
Various crimping processes, composite fibers, and the like have been tried, but the objectives have not been achieved yet. Recent advances in fibrillating technology for synthetic fibers have made it possible to fabricate fibrillated fibers. One example of such a technique is shown in Japanese Patent Publication No. 53-35633 and Japanese Patent Publication No. 56-16231. As a specific example, a composite type polyester filament made of polyamide and polyester is benzyl alcohol having a swelling ability for polyamide. Although there is a method of making fibrils by such treatments, there are the following problems in implementation, and the actual situation is that there are restrictions in operation.
1) 特公昭53-35633号公報の方法によれば、ベ
ンジルアルコール濃度1.5%以上の乳化水溶液で編織
物を処理するとあるが、この場合に処理された編織物中
の残留ベンジルアルコールが除去され難いため染め斑が
多発し、実際上、商品として望ましくない。また該薬剤
は高価であるために経済上の制約がある。さらに高濃度
の使用の場合に薬剤(ベンジルアルコール)の排液処理
に多大のコストが必要となる。1) According to the method of Japanese Patent Publication No. 53-35633, a knitted fabric is treated with an emulsified aqueous solution having a benzyl alcohol concentration of 1.5% or more. In this case, residual benzyl alcohol in the treated knitted fabric is removed. Since it is difficult to be applied, stains frequently occur, which is actually not desirable as a product. In addition, since the drug is expensive, there are economic restrictions. When using a higher concentration, a great deal of cost is required for the liquid waste treatment of the drug (benzyl alcohol).
2) 特公昭56-16231号公報の方法によれば、一
例としてポリビニルアルコールを編織物に付着させた後
にベンジルアルコールで処理し、フイブリル化するとあ
る。しかしこの場合に、編織物に対しポリビニルアルコ
ールの付着を均一にすることが不可能なために該方法で
得られた編織物は染色で染め斑が起こりやすく品質上好
ましくない。また該方法は処理工程が複雑でありコスト
的に高価なものとなる。2) According to the method of Japanese Patent Publication No. 56-16231, for example, polyvinyl alcohol is applied to a knitted fabric and then treated with benzyl alcohol to form a fibril. However, in this case, since it is impossible to make the adhesion of polyvinyl alcohol to the knitted fabric uniform, the knitted fabric obtained by the method is likely to cause uneven dyeing by dyeing, which is not preferable in terms of quality. In addition, the processing steps of this method are complicated and the cost is high.
3) ベンジルアルコールのポリアミドへの膨潤作用で
は、複合繊維を構成するポリアミドの長さ方向への収縮
が大きく、布帛上では緻密になり過ぎその調節が困難と
なる。また該薬剤が布帛上に残留した場合に編織物のヒ
ートセツトの時に風合が硬くなる等の問題がある。3) Due to the swelling action of benzyl alcohol on the polyamide, the polyamide constituting the composite fiber is largely shrunk in the lengthwise direction and becomes too dense on the cloth, and its adjustment becomes difficult. Further, when the chemical remains on the cloth, there is a problem that the texture becomes hard during heat setting of the knitted fabric.
本発明者らは上記の欠点を改良し、布帛の表面が天然繊
維に似たソフト感を有する風合及び上品な光沢の表面外
観を与え、適度の収縮を持たせて緻密かつ染め斑を殆ん
ど起こさない布帛物を得ること、及び薬剤コスト、工程
上等で工業的に有利な製造方法を提供することを目的と
して鋭意検討の結果、本発明に到達したものである。The present inventors have improved the above-mentioned drawbacks, provided the surface of the fabric with a soft feeling similar to natural fibers and a surface appearance with an elegant luster, and have a moderate shrinkage to give a dense and almost uneven dyeing. The present invention has been achieved as a result of earnest studies for the purpose of obtaining a fabric material that does not easily occur, and providing a manufacturing method that is industrially advantageous in terms of drug cost, process, and the like.
即ち、本発明は、ポリエステル部とポリアミド部からな
る分割剥離型マルチ複合フイラメントを含む布帛を湿潤
下で処理し、該複合フイラメントを高度に分割剥離して
フイブリル化するフイブリル化布帛物の製造法におい
て、安息香酸を0.6重量%以上3重量%以下含有しか
つ光線透過率が6%以下の濁度の乳化状態となるように
界面活性剤を添加した95℃以上130℃未満の熱水中
で該布帛に衝突および/または撹拌作用を与えて該布帛
を処理し、さらにアルカリ性水溶液にて処理することを
特徴とするフイブリル化布帛物の製造法である。That is, the present invention is a method for producing a fibrillated fabric in which a fabric containing a split-peeling multi-composite filament consisting of a polyester part and a polyamide part is treated under a wet condition, and the composite filament is highly split and fibrillated. Hot water of 95 ° C or higher and lower than 130 ° C containing benzoic acid in an amount of 0.6% by weight or more and 3% by weight or less and having a surfactant added so as to be in an emulsified state with a light transmittance of 6% or less The method for producing a fibrillated fabric is characterized in that the fabric is treated with a collision and / or stirring action to treat the fabric, and further treated with an alkaline aqueous solution.
本発明において用いられるポリエステル部とポリアミド
部からなる分割剥離型マルチ複合フイラメントは、ポリ
エステル部とポリアミド部とが単一フイラメント内で一
例として第1図に示す如き横断面を有するマルチフイラ
メントを指す。The split release type multi-composite filament comprising a polyester part and a polyamide part used in the present invention refers to a multifilament in which the polyester part and the polyamide part have a cross section as shown in FIG. 1 as an example within a single filament.
該複合フイラメントの一成分であるポリエステルとは主
成分がエチレンテレフタレート単位であり、必要により
他成分が約15モル%以下共重合されていても良い。他
成分としてはジエチレングリコール、ネオペンチルグリ
コール、シクロヘキサンジメタノール、イソフタル酸、
スルホイソフタル酸、ポリアルキレングリコール等の共
重合成分が挙げられ、更には添加物(例えば顔料、カー
ボン、シリカ等)、制電性向上剤(例えばポリエチレン
グリコール、末端に を有するポリアルキレングリコール、ドデシルベンゼン
スルホン酸等)、難燃剤あるいは染色性改良剤などを含
んでいてもよい。また複合成分の一成分であるポリアミ
ドとしては、ナイロン4、ナイロン6、ナイロン66、
ナイロン10等の脂肪族ポリアミド、ポリキシレンアジ
パミド、ポリヘキサメチレンフタラミド等の芳香族ポリ
アミド等が挙げられる。本発明で言う該複合フイラメン
トを含む布帛とは、該複合フイラメントを緯糸あるいは
経糸のいずれか、または両方に使用して織物にしたもの
や編物にしたものなどが挙げられる。The main component of the polyester, which is one component of the composite filament, is an ethylene terephthalate unit, and if necessary, the other component may be copolymerized in an amount of about 15 mol% or less. Other components include diethylene glycol, neopentyl glycol, cyclohexanedimethanol, isophthalic acid,
Copolymer components such as sulfoisophthalic acid and polyalkylene glycol can be mentioned, and further, additives (eg pigment, carbon, silica etc.), antistatic agent (eg polyethylene glycol, terminal A polyalkylene glycol, dodecylbenzene sulfonic acid or the like), a flame retardant or a dyeability improving agent. Polyamide, which is one component of the composite component, includes nylon 4, nylon 6, nylon 66,
Examples thereof include aliphatic polyamide such as nylon 10 and aromatic polyamide such as polyxylene adipamide and polyhexamethylene phthalamide. Examples of the cloth including the composite filament referred to in the present invention include those obtained by using the composite filament in either or both of the weft yarns and the warp yarns into a woven fabric or a knitted fabric.
本発明に用いられる界面活性剤としてはアニオン系活性
剤、カチオン系活性剤、ノニオン系活性剤、両性活性剤
等のいずれのものでもよいが、処理液に用いる安息香酸
の水に対する溶解度を減少せしめるもので、乳化分散さ
せる作用のあることが望ましい。The surfactant used in the present invention may be any of anionic surfactants, cationic surfactants, nonionic surfactants, amphoteric surfactants, etc., but it reduces the solubility of benzoic acid used in the treatment liquid in water. It is desirable that they have a function of emulsifying and dispersing.
即ち、本来安息香酸は熱水に溶けやすく、熱水に溶解し
た状態では、該複合フイラメントに対して膨潤効果がな
く該布帛を高度に収縮させることが不可能である。本発
明者らは推察するとこでは安息香酸の水へ完全溶解した
状態では、ポリエステルと分散染料の染着原理で知られ
るように、同じ分配率の法則によつて水相の方に安息香
酸の分配が大きく、ポリエステル及びポリアミドのよう
な疎水性の相の系には安息香酸が分配しにくいためだろ
うと考えられる。従つて、安息香酸の水に対する溶解度
を少くした乳化分散した状態では水−ポリエステル/ポ
リアミドの二相の系でポリエステル/ポリアミドの相に
分配が大きくなり、結果としてポリエステル及びポリア
ミドに対し安息香酸の親和力が増大し高度に膨潤収縮し
やすくなり、フイブリル化が可能になつたと考えられ
る。That is, originally, benzoic acid is easily soluble in hot water, and when dissolved in hot water, it has no swelling effect on the composite filament and it is impossible to highly shrink the fabric. According to the inference by the present inventors, in the state where benzoic acid is completely dissolved in water, as is known by the dyeing principle of polyester and disperse dye, the benzoic acid of benzoic acid is added to the water phase according to the same law of distribution ratio. It is thought that this is because benzoic acid is hard to partition into a system of hydrophobic phase such as polyester and polyamide, which has a large partitioning. Therefore, in an emulsion-dispersed state in which benzoic acid has a low solubility in water, in a two-phase system of water-polyester / polyamide, the distribution into the polyester / polyamide phase becomes large, and as a result, the affinity of benzoic acid for polyester and polyamide is increased. It is thought that the fibrils became possible because the swelling increased and the swelling and contraction became easy.
安息香酸の処理液の濃度としては0.6重量%以上とす
る必要があり、0.6重量%より低くなると本発明の狙
いとする充分な作用効果は得られなくなる。処理濃度の
上限としては3重量%が好ましく、それを越えると安息
香酸の乳化分散が不安定となり取り扱い性の面から不都
合である。The concentration of the treatment liquid of benzoic acid needs to be 0.6% by weight or more, and if it is lower than 0.6% by weight, the sufficient effect of the present invention cannot be obtained. The upper limit of the treatment concentration is preferably 3% by weight, and if it exceeds the upper limit, the emulsified dispersion of benzoic acid becomes unstable, which is inconvenient in terms of handleability.
本発明の方法で安息香酸を乳化分散せしめた水溶液の濁
度は測定温度70℃、波長400mμでの光透過率で上
限6%以下が好ましい。6.0%を越えると前記の理由
によるためか安息香酸による膨潤収縮の効果がなく布帛
にソフト感の大きい風合、及び緻密な布帛物にならない
ので不都合である。The turbidity of the aqueous solution in which benzoic acid is emulsified and dispersed by the method of the present invention is preferably at most 6% in terms of light transmittance at a measurement temperature of 70 ° C. and a wavelength of 400 mμ. If it exceeds 6.0%, there is no effect of swelling / shrinkage due to benzoic acid for the reason described above, and the fabric has a large soft feeling, and a dense fabric is not obtained, which is inconvenient.
なお本発明における透過率は日立製作所(株)製100−
40形分光光度計を使用して次の条件にて測定した。The transmittance in the present invention is 100- manufactured by Hitachi, Ltd.
It measured on the following conditions using the 40 type spectrophotometer.
測定セル:液槽10mm角形石英製 対照液:蒸留水、光源:タングステンランプ 波長:400mμ 測定温度:70℃ 上記の本発明における安息香酸の乳化水溶液で処理する
温度としては95℃以上が必要であり、95℃より低く
なると膨潤収縮が小さく緻密な布帛になり難く本発明の
狙いとするソフト感の大きい風合を有することが出来な
い。また上限の温度としては130℃であることが必要
であり、130℃以上では、本発明で用いられる布帛を
構成する複合フイラメントの一成分であるポリアミドの
重合度に低下を来たし、布帛の強度が低下するので不都
合である。Measurement cell: Liquid tank 10 mm square quartz Control solution: Distilled water, Light source: Tungsten lamp Wavelength: 400 mμ Measurement temperature: 70 ° C. The treatment temperature with the emulsified aqueous solution of benzoic acid according to the present invention must be 95 ° C. or higher. When the temperature is lower than 95 ° C., the swelling / shrinkage is small and it is difficult to form a dense fabric, and it is not possible to have the feeling of softness, which is the object of the present invention. Further, the upper limit temperature is required to be 130 ° C., and at 130 ° C. or higher, the degree of polymerization of polyamide, which is one component of the composite filament constituting the cloth used in the present invention, is lowered, and the strength of the cloth is reduced. It is inconvenient because it decreases.
本発明方法においては、安息香酸の乳化水溶液によつて
布帛に衝突、撹乱作用を与える必要があり、そのような
処理機械装置としては、高圧液流機、高圧ワツシヤー機
が望ましい。また、しわの入りやすい布帛については高
圧液流機が好適である。連続リラツクサ機では上記の衝
突及び撹乱作用がなく、フイブリル化が不可能であり、
不適である。In the method of the present invention, it is necessary to collide and disturb the cloth with the emulsified aqueous solution of benzoic acid. As such a processing machine, a high pressure liquid flow machine and a high pressure washer machine are preferable. A high-pressure liquid flow machine is suitable for a fabric that is prone to wrinkles. The continuous reflex machine does not have the above-mentioned collision and disturbance effects, and cannot be fibrillated.
Not suitable.
さらに本発明方法においては、安息香酸の乳化水溶液で
布帛に衝突、撹乱作用を与えた後に、炭酸ナトリウム、
水酸化ナトリウム等のアルカリ性水溶液にて浸漬処理す
る方法が用いられる。この場合の効果としては、布帛の
表面に残留する安息香酸を中和溶解し除去すると共に、
ポリエステル部とポリアミド部の境界線の未剥離部を完
全に消失させることにより、天然繊維の風合に似たソフ
ト感が大きく、均染性を有し安息香酸が実質的に除去さ
れていることより酸による弊害を有さない布帛を得るこ
とが出来る。この時の使用するアルカリ性水溶液のアル
カリ濃度は水素イオン濃度としてPH11〜13の範囲が
好適である。PH11未満では布帛上に残留した安息香酸
を中和し溶解除去するのに不充分であり、不都合であ
る。PH13を越えるとポリエステル部の溶解が進み大き
な重量減少を伴い、布帛にへたりが見られる場合が生じ
てくるので好ましくない。処理温度としては本発明の作
用効果の点より40℃以下の温度が好ましい。Furthermore, in the method of the present invention, after the fabric is collided with the emulsified aqueous solution of benzoic acid to give a disturbing effect, sodium carbonate,
A method of immersion treatment with an alkaline aqueous solution such as sodium hydroxide is used. As an effect in this case, the benzoic acid remaining on the surface of the fabric is neutralized and dissolved to be removed, and
By completely eliminating the unpeeled part of the boundary line between the polyester part and the polyamide part, a soft feeling similar to the feel of natural fiber is large, level dyeability and benzoic acid are substantially removed. It is possible to obtain a fabric that is free from the harmful effects of acid. The alkaline concentration of the alkaline aqueous solution used at this time is preferably in the range of PH 11 to 13 as the hydrogen ion concentration. If it is less than PH11, it is not sufficient to neutralize and dissolve and remove the benzoic acid remaining on the fabric, which is inconvenient. If it exceeds PH13, the polyester part will be dissolved and the weight will be greatly reduced, and the fabric may be sagged, which is not preferable. As the treatment temperature, a temperature of 40 ° C. or lower is preferable from the viewpoint of the effects of the present invention.
以下に本発明方法を実施例により説明し、実施に際して
必要な事項について説明する。もつとも本発明方法は、
以下の実施例の範囲に限定されるものではない。なお実
施例中のdr/fはデニール/フイラメント数を表わし、
〔η〕(固有粘度)はテトラクロエタン:フエノール=
1:1の混合溶媒を用いて30℃で測定した固有粘度
(dl/g)の値である。Hereinafter, the method of the present invention will be described by way of examples, and matters necessary for carrying out the method will be described. The method of the present invention is
It is not limited to the scope of the following examples. Note that dr / f in the examples represents the number of denier / filament,
[Η] (intrinsic viscosity) is tetrachloroethane: phenol =
It is a value of intrinsic viscosity (dl / g) measured at 30 ° C. using a mixed solvent of 1: 1.
実施例1及び比較例1〜4 〔η〕1.23のナイロン6及び〔η〕0.68のポリ
エチレンテレフタレート(PETと略す)のチツプを用
いて、ナイロン6/PETの複合比率が1/2でありそ
の横断面が第1図に示すもので、ナイロン6が5層、P
ETが6層の貼り合せ型となるように紡糸温度290℃
で紡糸速度1010m/分の紡糸条件下で巻取り分離剥
離型複合フイラメントの未延伸糸を得た。次いでこの未
延伸糸を77℃の熱ローラ及び150℃の熱プレートに
接触させて3.49倍に延伸して75dr/24fの複合
フイラメントを得た。このフイラメントを用いてタフタ
を製織した。この生機密度は経糸90本/吋、緯糸86
本/吋であつた。このタフタを糊抜き処理した後に第1
表に示した浴組成の条件にて浴比10:1で液流方式の
処理装置を用いて120℃30分間の処理を行つた。更
に水酸化ナトリウム2g/(PH約13)にて室温下2
0分間処理を行つた。次いで充分に水洗しプレセツト1
70℃の熱処理をピンテンターで行い、染色を行つた。
フイブリル化度、面積収縮率、風合(ソフト感)、染め
斑の結果について第1表に示す。なお上記染色としては
次の染色条件を用いた。Example 1 and Comparative Examples 1 to 4 Nylon 6 of [η] 1.23 and polyethylene terephthalate (abbreviated as PET) of [η] 0.68 were used, and the composite ratio of nylon 6 / PET was 1/2. And its cross section is shown in Fig. 1. Nylon 6 has 5 layers, P
Spinning temperature is 290 ° C so that ET is a 6-layer laminated type
The unstretched yarn of the take-up separation separation type composite filament was obtained under the spinning conditions of spinning speed 1010 m / min. Next, this unstretched yarn was brought into contact with a heat roller at 77 ° C. and a heat plate at 150 ° C. and drawn 3.49 times to obtain a composite filament of 75 dr / 24f. Taffeta was woven using this filament. This greige density is 90 warps / inch, 86 wefts
It was a book / inch. After the desizing process of this taffeta, the first
Under the conditions of the bath composition shown in the table, the treatment was carried out at 120 ° C. for 30 minutes using a liquid flow type treatment apparatus at a bath ratio of 10: 1. 2 g of sodium hydroxide / (PH about 13) at room temperature 2
The treatment was carried out for 0 minutes. Then, rinse thoroughly with water and press 1
Dyeing was performed by heat treatment at 70 ° C. with a pin tenter.
Table 1 shows the results of the degree of fibrillation, the area shrinkage rate, the feel (soft feeling), and the uneven dyeing. The following dyeing conditions were used for the above dyeing.
染色: なおフイブリル化度は、処理後の織物を構成する経糸及
び緯糸について光学顕微鏡で観察し複合二成分の分離剥
離程度を評価したものであり、評価基準は次の通りであ
る。staining: The degree of fibrillation is the degree of separation and peeling of the composite two components evaluated by observing the warp and the weft constituting the treated fabric with an optical microscope, and the evaluation criteria are as follows.
フイブリル化度評価 また面積収縮率については、以下に示すように処理後の
面積収縮率について測定し、そと膨潤収縮性について調
べたものである。Evaluation of fibrillation degree As for the area shrinkage, the area shrinkage after the treatment was measured and the swelling and shrinkability was investigated as shown below.
S1:織物の経方向の収縮率(%) l0:処理前経方向の長さ l1:処理後の経方向の長さ S2:織物の緯方向の収縮率(%) l2:処理前緯方向の長さ l3:処理後の緯方向の長さ なお第1表には、浴組成として界面活性剤を添加しない
状態(比較例1)、安息香酸を添加しない状態(比較例
2)、界面活性剤と安息香酸の両方を添加しない状態
(比較例3)、安息香酸を従来一般に用いられているベ
ンジルアルコールに変えた状態(比較例4)の結果を併
記する。 S 1 : Shrinkage rate (%) in the warp direction of the fabric l 0 : Length in the warp direction before treatment l 1 : length in warp direction after treatment S 2 : shrinkage ratio (%) in weft direction of woven fabric l 2 : length in weft direction before treatment l 3 : length in the latitudinal direction after treatment In Table 1, a condition that the surfactant is not added as a bath composition (Comparative Example 1), a condition that benzoic acid is not added (Comparative Example 2), and a surfactant are shown. The results of a state in which both benzoic acids are not added (Comparative Example 3) and a state in which benzoic acid is changed to benzyl alcohol which is generally used conventionally (Comparative Example 4) are also shown.
第1図は、本発明において使用される分割剥離型の複合
フイラメントの一例の横断面図である。図面において、
空白部はポリエステル部、斜線部はポリアミド部を示
す。FIG. 1 is a cross-sectional view of an example of a split peel type composite filament used in the present invention. In the drawing,
The blank portion indicates the polyester portion and the shaded portion indicates the polyamide portion.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 徳永 勲 岡山県倉敷市酒津1621番地 株式会社クラ レ内 (72)発明者 佐藤 正典 岡山県倉敷市酒津1621番地 株式会社クラ レ内 (72)発明者 山口 新司 岡山県倉敷市酒津1621番地 株式会社クラ レ内 (56)参考文献 特開 昭56−73168(JP,A) 特公 昭39−933(JP,B1) 特公 昭53−35633(JP,B1) ─────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Isao Tokunaga 1621 Sakurazu, Kurashiki-shi, Okayama Prefecture Kuraray Co., Ltd. (72) Inventor Masanori Sato 1621 Satsuki, Kurashiki-shi, Okayama Uchi, Kuraray Co., Ltd. (72) Inventor Shinji Yamaguchi 1621 Sakata, Kurashiki City, Okayama Prefecture Kuraray Co., Ltd. (56) Reference JP-A-56-73168 (JP, A) JP-B 39-933 (JP, B1) JP-B 53-35633 (JP, B1)
Claims (1)
割剥離型マルチ複合フイラメントを含む布帛を湿潤下で
処理し、該複合フイラメントを高度に分離剥離してフイ
ブリル化するフイブリル化布帛物の製造法において、安
息香酸を0.6重量%以上3重量%以下含有しかつ光線
透過率が6%以下の濁度の乳化状態となるように界面活
性剤を添加した95℃以上130℃未満の熱水中で該布
帛に衝突および/または撹拌作用を与えて該布帛を処理
し、さらにアルカリ性水溶液にて処理することを特徴と
するフイブリル化布帛物の製造法。1. A method for producing a fibrillated fabric, which comprises treating a fabric containing a split-peelable multi-composite filament consisting of a polyester part and a polyamide part under wet conditions to highly separate and exfoliate the fibril into a fibrillated fabric. In hot water of 95 ° C or higher and lower than 130 ° C, containing benzoic acid in an amount of 0.6% by weight or more and 3% by weight or less and having a surfactant added so as to be in an emulsified state with a light transmittance of 6% or less. A process for producing a fibrillated fabric, which comprises subjecting the fabric to collision and / or stirring to treat the fabric, and further treating the fabric with an alkaline aqueous solution.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60073338A JPH0657909B2 (en) | 1985-04-05 | 1985-04-05 | Method for manufacturing fibrillated fabric |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60073338A JPH0657909B2 (en) | 1985-04-05 | 1985-04-05 | Method for manufacturing fibrillated fabric |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61231264A JPS61231264A (en) | 1986-10-15 |
| JPH0657909B2 true JPH0657909B2 (en) | 1994-08-03 |
Family
ID=13515270
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60073338A Expired - Fee Related JPH0657909B2 (en) | 1985-04-05 | 1985-04-05 | Method for manufacturing fibrillated fabric |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0657909B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6385166A (en) * | 1986-09-22 | 1988-04-15 | 帝人株式会社 | Production of ultrafine fiber knitted fabric |
| JP2613240B2 (en) * | 1988-02-25 | 1997-05-21 | 株式会社クラレ | Synthetic fiber cloth processing method |
| JPH02145812A (en) * | 1988-11-28 | 1990-06-05 | Kuraray Co Ltd | Conjugate fiber and treatment of cloth using the same |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5673168A (en) * | 1979-11-10 | 1981-06-17 | Kanebo Ltd | Production of knitted fabric |
-
1985
- 1985-04-05 JP JP60073338A patent/JPH0657909B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61231264A (en) | 1986-10-15 |
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