JPH07126919A - Pile raw yarn for electric transplantation - Google Patents
Pile raw yarn for electric transplantationInfo
- Publication number
- JPH07126919A JPH07126919A JP27544893A JP27544893A JPH07126919A JP H07126919 A JPH07126919 A JP H07126919A JP 27544893 A JP27544893 A JP 27544893A JP 27544893 A JP27544893 A JP 27544893A JP H07126919 A JPH07126919 A JP H07126919A
- Authority
- JP
- Japan
- Prior art keywords
- hot water
- acid
- polymer component
- pile
- soluble polymer
- 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
Links
- 238000002054 transplantation Methods 0.000 title abstract 2
- 239000000835 fiber Substances 0.000 claims abstract description 39
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229920000728 polyester Polymers 0.000 claims abstract description 8
- 229920001515 polyalkylene glycol Polymers 0.000 claims abstract description 3
- 229920000642 polymer Polymers 0.000 claims description 29
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 18
- KKEYFWRCBNTPAC-UHFFFAOYSA-N terephthalic acid group Chemical group C(C1=CC=C(C(=O)O)C=C1)(=O)O KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 12
- 229920001634 Copolyester Polymers 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 10
- 239000002131 composite material Substances 0.000 claims description 10
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 10
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 4
- 150000002009 diols Chemical class 0.000 claims description 4
- 244000144992 flock Species 0.000 claims description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- 238000002513 implantation Methods 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- IBBQVGDGTMTZRA-UHFFFAOYSA-N sodium;2-sulfobenzene-1,3-dicarboxylic acid Chemical compound [Na].OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O IBBQVGDGTMTZRA-UHFFFAOYSA-N 0.000 claims description 2
- 238000004581 coalescence Methods 0.000 claims 1
- 229920001410 Microfiber Polymers 0.000 abstract description 13
- 238000004043 dyeing Methods 0.000 abstract description 13
- 239000003960 organic solvent Substances 0.000 abstract description 3
- 125000002091 cationic group Chemical group 0.000 abstract description 2
- 239000000975 dye Substances 0.000 abstract description 2
- 230000001268 conjugating effect Effects 0.000 abstract 2
- 229920003176 water-insoluble polymer Polymers 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 1
- 230000002349 favourable effect Effects 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 description 19
- 239000000853 adhesive Substances 0.000 description 10
- 230000001070 adhesive effect Effects 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 239000004744 fabric Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229920002292 Nylon 6 Polymers 0.000 description 5
- 238000009987 spinning Methods 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000009991 scouring Methods 0.000 description 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000002932 luster Substances 0.000 description 3
- 238000002074 melt spinning Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- 239000004902 Softening Agent Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 239000013043 chemical agent Substances 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- 238000009990 desizing Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 230000005802 health problem Effects 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 206010016322 Feeling abnormal Diseases 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 239000003522 acrylic cement Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 150000001768 cations Chemical group 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- VOMXDGJBICHGCV-UHFFFAOYSA-L dipotassium;propan-2-yl phosphate Chemical compound [K+].[K+].CC(C)OP([O-])([O-])=O VOMXDGJBICHGCV-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Artificial Filaments (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Multicomponent Fibers (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、高密度で集束性の良
い、発色性の良好な極細繊維の電気植毛品が可能な電気
植毛用パイル原糸に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a pile yarn for electric flocking, which can be used for electric flocking of ultrafine fibers having a high density, a good focusing property, and a good coloring property.
【0002】[0002]
【従来の技術】パイル原糸を短くカットした繊維を静電
気により基布に接着剤を介して植毛した製品は種々の用
途に利用されているが、製品の表面品位や触感性に優れ
た極細繊維の電気植毛品の開発が、従来より種々なされ
ている。2. Description of the Related Art Products obtained by statically flocking fibers obtained by cutting pile raw yarns into a base fabric with an adhesive agent are used for various purposes, but are extremely fine fibers with excellent surface quality and tactile sensation. Various developments have been made in the past for electric flocking products.
【0003】極細繊維を植毛する方法としては、2成分
の複合繊維を植毛した後、1成分を溶解除去、または膨
潤分割処理して極細化する手段が知られている。As a method for flocking ultrafine fibers, there is known a means for flocking bicomponent composite fibers, and then dissolving and removing one component or swelling and dividing treatment to obtain ultrafine fibers.
【0004】しかしながら、これら1成分を溶解除去、
または膨潤分割処理には化学薬品を用いざるを得なかっ
た。例えば特開昭59−76975号公報や特開昭60
−155745号公報に開示されているように、海成分
としてポリスチレンを用いる場合は、植毛後の海成分の
溶解除去にトリクレンが必要であった。また、海成分と
してナイロン6を用いる場合は、植毛後の海成分の溶解
除去にギ酸が必要であり、ポリエステルとナイロン6の
複合繊維でナイロン6を膨潤させて分割する場合には、
ベンジルアルコールが必要であった。これらの化学薬品
の取扱いは危険性があり、溶解除去あるいは膨潤分割処
理のための特殊な設備が必要である。このため、作業者
の安全衛生面および製造コスト面に問題があった。さら
に、植毛後のこれら化学薬品の使用は、パイル植毛に使
用する接着剤を老化させたり、膨潤させたりしてパイル
抜けを生じたり、脆化させて製品風合いを損なうという
欠点があった。However, these one component is dissolved and removed,
Alternatively, chemical agents had to be used for the swelling division treatment. For example, JP-A-59-76975 and JP-A-60-
As disclosed in Japanese Patent Laid-Open No. 155745, when polystyrene is used as the sea component, trichlene is necessary for dissolving and removing the sea component after flocking. When nylon 6 is used as the sea component, formic acid is required to dissolve and remove the sea component after the flocking, and when swelling the nylon 6 with the composite fiber of polyester and nylon 6 to divide it,
Benzyl alcohol was needed. The handling of these chemicals is dangerous and requires special equipment for dissolution removal or swelling separation treatment. For this reason, there are problems in terms of worker safety and health and manufacturing costs. Further, the use of these chemicals after flocking has a drawback in that the adhesive used for flocking piles is aged or swollen to cause pile loss, or it is embrittled to impair the product texture.
【0005】一方、上記欠点を改善するため、水溶性の
高分子重合体からなる複合繊維をパイル原糸に用いて水
系除去を可能にした技術が、特開昭63−84668号
公報に開示されている。ただ、水溶性の高分子重合体で
は常温水にも溶けるため、製糸工程での油剤エマルジョ
ン付与時や液浴延伸時、およびフロック加工工程での水
溶液処理時などで、極細繊維化したり、繊維同志の膠着
などがあった。また、高温での染色を要しその作業性の
負担とともに製品品位を損なうなど、必ずしも満足のい
くものは得られなかった。すなわち、安定的な極細繊維
の電気植毛品の提供には限界があった。On the other hand, in order to improve the above-mentioned drawbacks, a technique in which a composite fiber made of a water-soluble high-molecular polymer is used as a pile raw yarn to enable removal of an aqueous system is disclosed in JP-A-63-84668. ing. However, since water-soluble high-molecular weight polymers are soluble in water at room temperature, they can be made into ultrafine fibers when the oil emulsion is applied in the spinning process, when the liquid bath is stretched, and when the aqueous solution is processed in the flocking process. There was a stalemate. In addition, satisfactory results were not obtained, such as dyeing at high temperature, which impairs workability and impairs product quality. In other words, there has been a limit to the provision of stable ultrafine fiber electric flocking products.
【0006】[0006]
【発明が解決しようとする課題】本発明は、前述したよ
うな従来技術の欠点のない良好な極細繊維の電気植毛品
が得ることができる電気植毛用パイル原糸の提供を目的
とする。SUMMARY OF THE INVENTION It is an object of the present invention to provide a pile yarn for electric flocking, which can obtain a good electric flocked product of ultrafine fibers without the above-mentioned drawbacks of the prior art.
【0007】[0007]
【課題を解決するための手段】本発明の目的は、少なく
とも2成分以上からなる複合繊維であって、熱水溶解性
重合体成分と、熱水に不溶解性でかつ常圧可染性である
他の重合体成分からなり、前記熱水溶解性重合体成分の
少なくとも一部が繊維表面を形成するように合流・複合
された可細化性繊維であることを特徴とする電気植毛用
パイル原糸によって達成される。The object of the present invention is a composite fiber comprising at least two components, which is a hot water-soluble polymer component and is insoluble in hot water and dyeable under normal pressure. A pile for electro-implantation, comprising a certain other polymer component, and at least a part of the hot water-soluble polymer component is a comminuted fiber which is joined and composited so as to form a fiber surface. Achieved by the raw yarn.
【0008】以下本発明を詳細に説明する。まず、本発
明にかかる可細化性繊維について述べる。本発明におけ
る可細化性繊維は少なくとも2成分の重合体からなり、
公知の海島型あるいは分割型の断面形態を有するもので
ある。The present invention will be described in detail below. First, the thinnable fiber according to the present invention will be described. The micronizable fiber in the present invention is composed of a polymer of at least two components,
It has a known sea-island type or divided type cross-sectional shape.
【0009】可細化性繊維の一方の成分は溶融紡糸に耐
え、かつ熱水に溶解する熱水溶解性重合体よりなるもの
とする。かかる熱水溶解性重合体は、公知のものが適用
でき、特に限定されるものではない。そして特に好まし
いものとしては5−ナトリウムスルホイソフタル酸など
を共重合した各種のポリエステル、例えば下記Aおよび
Bの重合体が挙げられる。 A.主たる酸成分がテレフタル酸であって、他の酸成分
は8〜15mol%の5−ナトリウムスルホイソフタル
酸、および5〜40mol%のイソフタル酸であり、主
たるジオール成分がエチレングリコールよりなる共重合
ポリエステルである共重合ポリエステル。One component of the micronizable fiber is a hot water-soluble polymer that is resistant to melt spinning and is soluble in hot water. As the hot water-soluble polymer, known polymers can be applied and are not particularly limited. Particularly preferable examples include various polyesters copolymerized with 5-sodium sulfoisophthalic acid and the like, for example, the polymers of A and B below. A. The main acid component is terephthalic acid, the other acid components are 8 to 15 mol% 5-sodium sulfoisophthalic acid, and 5 to 40 mol% isophthalic acid, and the main diol component is a copolyester composed of ethylene glycol. A copolyester.
【0010】B.主たる酸成分がテレフタル酸であっ
て、他の酸成分は1〜15mol%の5−ナトリウムス
ルホイソフタル酸、および20mol%以下のイソフタ
ル酸であり、主たるジオール成分がエチレングリコール
とビスフェノールAのエチレンオキシド付加物よりなる
共重合ポリエステル。 これらの重合体は、高温の溶融紡糸に耐え、常温水には
溶けずにしかも熱水に容易に溶け、しかも低価格である
ので好ましいものである。B. The main acid component is terephthalic acid, the other acid components are 1 to 15 mol% 5-sodium sulfoisophthalic acid, and 20 mol% or less isophthalic acid, and the main diol component is ethylene glycol adduct of bisphenol A with ethylene oxide. A copolyester consisting of. These polymers are preferable because they can withstand high temperature melt spinning, do not dissolve in room temperature water, easily dissolve in hot water, and are inexpensive.
【0011】次に本発明のかかる可細化性繊維の常圧可
染性の他の重合体成分について述べる。該重合体成分は
常圧で染色でき、かつ溶融紡糸が可能な重合体が任意に
適用できる。ここで常圧可染性であることが重要であ
る。ここで言う常圧可染とはキャリアー、膨潤剤などの
助剤の添加がなく実用的な染色ができることである。助
剤の添加は洗浄の繁雑さと環境衛生に欠点を生じる。ま
た従来の高温加圧の染色ではせっかく均一に植毛させた
パイルがへたったり、接着剤や基布の十分でない耐熱性
でパイル抜けや風合い硬化などが生じ、製品品位を損な
い要望されるものが得られない。かかる重合体成分とし
て好ましいものとしては、5−ナトリウムスルホイソフ
タル酸などを共重合してカチオン可染性に改質したポリ
エステルや、各種のポリアミド、例えば下記Aの重合体
が挙げられる。 A.テレフタル酸とエチレングリコールとを主たる構成
成分とし、全酸成分に対し1.5〜5.5mol%の5
−ナトリウムスルホイソフタル酸、および又は全ポリマ
ーに対し1〜10重量%のポリアルキレングリコールも
しくはその誘導体を含有する共重合ポリエステルである
共重合ポリエステル。Next, another polymer component of the present invention, which is capable of being dyed under atmospheric pressure, of the thinnable fiber will be described. As the polymer component, a polymer which can be dyed under normal pressure and which can be melt-spun can be optionally applied. Here, it is important that it is dyeable under normal pressure. Atmospheric pressure dyeing as used herein means that practical dyeing can be carried out without the addition of carriers, swelling agents and other auxiliary agents. The addition of auxiliaries causes drawbacks in cleaning complexity and environmental hygiene. In addition, conventional high-temperature and high-pressure dyeing causes the piles that have been flocked uniformly to become tired, and the insufficient heat resistance of adhesives and base fabrics causes the piles to fall off and the texture to harden, resulting in impaired product quality. I can't get it. Preferable examples of such a polymer component include polyester modified with cation dyeability by copolymerizing 5-sodium sulfoisophthalic acid and the like, and various polyamides such as the polymer of the following A. A. The main components are terephthalic acid and ethylene glycol, and 1.5 to 5.5 mol% of 5 with respect to all acid components.
A copolyester which is a copolyester containing sodium sulfoisophthalic acid and / or 1 to 10% by weight of the total polymer of a polyalkylene glycol or a derivative thereof.
【0012】なお、前述の重合体成分には、必要に応じ
て例えば、艶消し剤、安定剤、制電剤、防炎剤などの添
加剤を含有せしめてもよい。The above-mentioned polymer component may optionally contain additives such as a matting agent, a stabilizer, an antistatic agent and a flameproofing agent.
【0013】本発明における可細化性繊維の好適される
製造方法について述べる。まず熱水溶解性重合体と他の
重合体を各々独立に溶融し、次に熱水溶解性重合体が少
なくとも一部が繊維表面を形成するように、例えば海部
に熱水溶解性重合体が島部に他の重合体がなるように、
または他の重合体を熱水溶解性重合体が分割するように
両者を合流せしめ、紡糸口金の吐出孔から吐出し複合製
糸する。A preferred method for producing the thinnable fiber in the present invention will be described. First, the hot water-soluble polymer and the other polymer are independently melted, and then the hot water-soluble polymer forms a fiber surface at least partially, for example, the hot water-soluble polymer is So that the other polymer becomes on the island,
Alternatively, another polymer is merged so that the hot water-soluble polymer is divided, and the polymer is discharged from the discharge hole of the spinneret to form a composite yarn.
【0014】可細化性繊維の前記製法が満たされるもの
であれば、その他については限定されるものではなく、
任意の複合製糸方法が適用できる。そして、かかる方法
として特に好ましい方法は、いわゆる芯鞘法、高分子配
列体法、分割法が挙げられる。また、かかる他の重合体
は常圧可染のものであって、その発色性を損なわない範
囲で補強のためにより高重合度の重合体を芯とした、い
わゆる3成分の形態をとってもよい。繊維の断面形状な
どは特に限定されるものではなく、任意のものが適用で
きる。Others are not limited as long as the above-mentioned manufacturing method of the thinnable fiber is satisfied,
Any composite yarn making method can be applied. And as such a method, a so-called core-sheath method, polymer array method, and division method are particularly preferable. Further, such other polymer may be dyed under normal pressure, and may take a so-called three-component form in which a polymer having a higher degree of polymerization is used as a core for reinforcement as long as the color developability is not impaired. The cross-sectional shape of the fiber is not particularly limited, and any one can be applied.
【0015】前記方法の紡糸口金の吐出孔より吐出され
た複合繊維は高速で引取られ、そのまま実用の繊維とさ
れてもよいし、また比較的低速で引取り、さらに延伸し
て実用の繊維としてもよい。The composite fiber discharged from the discharge hole of the spinneret in the above method may be drawn at a high speed to be a practical fiber as it is, or may be drawn at a relatively low speed and further drawn to be a practical fiber. Good.
【0016】本発明の熱水溶解性重合体と他の重合体と
から形成される可細化性繊維において、熱水溶解性重合
体の成分比率が40重量%以下とする。より好ましくは
5〜30重量%である。5重量%未満では所望とする複
合断面の形態を保持するのが困難となりやすい。一方、
40重量%を越えると複合繊維の強力が低くなり、工程
通過性が悪くなったり、製品パイルの密度が粗くなり品
位が劣る場合がある。In the micronizable fiber formed from the hot water-soluble polymer of the present invention and another polymer, the component ratio of the hot water-soluble polymer is 40% by weight or less. It is more preferably 5 to 30% by weight. If it is less than 5% by weight, it tends to be difficult to maintain the desired shape of the composite cross section. on the other hand,
If it exceeds 40% by weight, the strength of the composite fiber may be lowered, the process passability may be deteriorated, and the product pile may have a low density and poor quality.
【0017】本発明における可細化性繊維の複合繊維に
おいては、可細化前の単糸繊度が1デニール以上50デ
ニール未満が好ましい。1デニール未満では電気植毛性
が劣り、50デニール以上とすると溶融紡糸時の冷却時
の製糸性が不安定となったり、電気植毛時の飛翔性に問
題が生じる。また、可細化性繊維は該熱水溶解性の成分
を除去すれば、2本以上の繊維に分かれる繊維であり、
この分かれた後の繊維の単糸繊度が0.5デニール以下
とすることである。0.5デニールを越えると、極細繊
維が持つ特有の光沢やしなやかさが不十分となる。In the conjugate fiber of the thinnable fiber in the present invention, the single yarn fineness before thinning is preferably 1 denier or more and less than 50 denier. If it is less than 1 denier, the electric flocking property is inferior, and if it is 50 denier or more, the spinning property during cooling during melt spinning becomes unstable, or the flight property during electric flocking becomes a problem. Further, the thinnable fiber is a fiber that is divided into two or more fibers by removing the hot water-soluble component,
The single-filament fineness of the separated fibers is to be 0.5 denier or less. When it exceeds 0.5 denier, the unique luster and flexibility of the ultrafine fibers become insufficient.
【0018】次に、電気植毛品の製造方法について述べ
る。まず、前記可細化性繊維のパイル原糸は従来より公
知の方法で所望の長さに切断される。カットパイル長は
電気植毛品の目的に応じて、また繊維の太さ、カットパ
イルの植毛条件によって決まるが、好ましくは0.5m
m以上、30mm以下、より好ましくは10mm以下で
ある。0.5mm未満では短すぎて極細繊維パイル品の
効果であるソフト感、特有の光沢やしなやかさが発揮さ
れにくく、30mmを越えるとパイルが倒れ、もつれて
しまいパイル品位が低下する。次いで該カットパイルを
非イオン活性剤の水溶液で精練した後、ケイ酸ソーダ、
コロイダルシリカ、イソプロピルホスフエートカリより
なる処理液で処理し、脱水、乾燥をする。Next, a method for manufacturing an electric hair transplant product will be described. First, the pile yarn of the thinnable fiber is cut into a desired length by a conventionally known method. The cut pile length depends on the purpose of the electric flocking product, the thickness of the fibers, and the flocking conditions of the cut pile, but is preferably 0.5 m.
It is m or more and 30 mm or less, more preferably 10 mm or less. If it is less than 0.5 mm, it is too short, and it is difficult to exhibit the soft feeling, unique luster and pliability, which are the effects of the ultrafine fiber pile product, and if it exceeds 30 mm, the pile collapses and becomes entangled to lower the pile quality. Then, after scouring the cut pile with an aqueous solution of a nonionic activator, sodium silicate,
It is treated with a treatment liquid containing colloidal silica and potassium isopropyl phosphate, dehydrated and dried.
【0019】一方、本発明のカットパイルを植毛する基
体としては、糸状物や織編物、不織布、および樹脂など
のシート状物など多くのものが用いられる。この基体に
該パイル原糸を接着させる接着剤を塗布する。接着剤と
してはアクリル系エマルジョン、エーテル型あるいはエ
ステル型ポリウレタンなどが用いられる。前記基体と接
着剤は、特に限定されることなく公知のものが用いられ
る。接着剤を塗布した基体にカットパイルを植毛する方
法としては、従来より公知の方法が用いられる。特に、
アップ方式による電気植毛が好ましく用いられる。On the other hand, as the substrate for implanting the cut pile of the present invention, many materials such as filamentous materials, woven and knitted materials, non-woven materials, and sheet materials such as resins are used. An adhesive for adhering the pile raw yarn is applied to this base. As the adhesive, acrylic emulsion, ether type or ester type polyurethane or the like is used. The substrate and the adhesive are not particularly limited, and known ones can be used. As a method for implanting the cut pile on the substrate coated with the adhesive, a conventionally known method is used. In particular,
Electric flocking by the up method is preferably used.
【0020】本発明のパイル原糸からなるカットパイル
を電気植毛したものは、まず熱水で処理され、熱水溶解
性成分を除去するための処理を実施する。熱水温度は8
0〜98℃が好ましい。この溶解処理は、通常の高次加
工工程、すなわち糊抜き精練の工程をはじめ、ウィン
ス、サーキュラーなどの染色方式を利用して溶解処理す
る。溶解処理には、トリポリリン酸などの軟水化剤を用
いることでより安定的な溶解除去が可能となる。なお、
糊抜きのための助剤、すなわち界面活性剤や再付着防止
剤や弱アルカリ剤などの使用は特に好ましい。次いで染
色仕上げを行う。染色は98℃以下で行う。このように
高次加工工程が、100℃未満の温度で加工でき、かつ
有機溶剤や強アルカリなどの薬剤を使うことなく加工で
きるため、極細繊維パイル品のパイル抜けや風合いの硬
化のような品位を損なうことなくできることをはじめ、
加圧密閉式や局所排気など特殊な設備が要らないこと、
安全環境衛生上の問題がない。The cut pile made of the raw yarn of pile of the present invention, which has been electroflocked, is first treated with hot water to carry out a treatment for removing hot water-soluble components. Hot water temperature is 8
0-98 degreeC is preferable. This dissolution treatment is performed by using a usual higher-order processing step, that is, a desizing and scouring step, and a dyeing method such as wince or circular. In the dissolution treatment, it is possible to more stably dissolve and remove by using a water softening agent such as tripolyphosphoric acid. In addition,
It is particularly preferable to use an auxiliary agent for desizing, that is, a surfactant, an anti-redeposition agent, a weak alkaline agent, or the like. Then, a dyeing finish is performed. Dyeing is performed at 98 ° C or lower. In this way, the high-order processing process can be performed at a temperature of less than 100 ° C and can be processed without using chemicals such as organic solvents and strong alkalis. Including what you can do without sacrificing
No need for special equipment such as pressure sealed type or local exhaust,
There are no safety, environmental and health problems.
【0021】[0021]
【実施例】以下、実施例により本発明を詳細に説明す
る。 実施例1 熱水溶解性重合体として12mol%の5−ナトリウム
スルホイソフタル酸、および25mol%のイソフタル
酸、そして酸化チタン0.05重量%を含んだ共重合ポ
リエチレンテレフタレートチップ(290℃での溶融粘
度:1500ポイズ,軟化点:130℃)を100℃で
10時間減圧乾燥したものを用いた。他の重合体として
5mol%の5−ナトリウムスルホイソフタル酸を含ん
だ共重合ポリエステルチップ(290℃での溶融粘度:
1800ポイズ,軟化点:250℃)を150℃で6時
間減圧乾燥したものを使用した。各々スクリュー押出機
で溶融(290℃)し、熱水溶解性重合体が海成分に、
他の重合体が島成分として、ギアポンプで海島型紡糸口
金に送り複合紡糸し、海成分比20%、島成分比80
%、島数16島、繊度11.5デニールの未延伸糸を得
た。得られた未延伸糸を90℃の熱板を通過させて延伸
し、3.8デニールの電気植毛用パイル原糸を得た。紡
糸、延伸時の糸切れは発生しなかった。The present invention will be described in detail below with reference to examples. Example 1 Copolyethylene terephthalate chips (melt viscosity at 290 ° C.) containing 12 mol% 5-sodium sulfoisophthalic acid as a hot water-soluble polymer, and 25 mol% isophthalic acid, and 0.05 wt% titanium oxide. (1,500 poise, softening point: 130 ° C.), which was dried under reduced pressure at 100 ° C. for 10 hours, was used. Copolymerized polyester chips containing 5 mol% 5-sodium sulfoisophthalic acid as another polymer (melt viscosity at 290 ° C .:
1800 poise, softening point: 250 ° C.) and dried under reduced pressure at 150 ° C. for 6 hours were used. Each was melted (290 ° C) with a screw extruder, and the hot water-soluble polymer became the sea component,
The other polymer is sent as an island component to the sea-island type spinneret by a gear pump and is subjected to complex spinning. The sea component ratio is 20%, the island component ratio is 80
%, The number of islands was 16 and the fineness was 11.5 denier. The undrawn yarn thus obtained was drawn by passing through a hot plate at 90 ° C. to obtain a 3.8 denier pile yarn for electric flocking. No yarn breakage occurred during spinning or drawing.
【0022】得られた電気植毛用パイル原糸を1mmに
カットし、このカットパイルを非イオン系活性剤含有水
溶液で精練した後、ケイ酸ソーダ、コロイダルシリカ、
シソプロピルホスフエートカリよりなる処理液に浸漬処
理し、脱水、乾燥して、電気植毛用パイルとした。この
パイルの表面電気抵抗は2×108 Ω・cmであった。The obtained pile yarn for electric flocking was cut into 1 mm, the cut pile was scoured with an aqueous solution containing a nonionic activator, and then sodium silicate, colloidal silica,
A pile for electric flocking was obtained by immersing in a treatment liquid containing potassium peroxophosphate and dehydration and drying. The surface electric resistance of this pile was 2 × 10 8 Ω · cm.
【0023】植毛する基布はアクリル紡毛糸の平織物
(目付120g/m2 )を用い、その片面に接着剤とし
てアクリル系エマルジョン(固形分30%)を200g
/m2となるようにナイフコータで塗布し、アップ法で
電気植毛した(電圧3万V、電極間距離10cm)。パ
イルの飛翔性には何の問題もなく、良好に植毛を完了し
た。パイルの植毛密度は140g/m2 であった。A plain fabric of acrylic woolen yarn (weight per unit area: 120 g / m 2 ) was used as a base fabric for flocking, and 200 g of an acrylic emulsion (solid content: 30%) was used as an adhesive on one side of the fabric.
/ M 2 was applied with a knife coater, and electric flocking was performed by the up method (voltage 30,000 V, distance between electrodes 10 cm). There was no problem with the flight properties of the pile, and the flocking was completed successfully. The pile flock density was 140 g / m 2 .
【0024】植毛したものを、120℃で乾燥、150
℃のキュアリングし、ウィンス染色機に投入たし。精練
助剤としてNaOH0.1%、トリポリリン酸0.2g
/l、界面活性剤2g/lをいれ90℃、10分の熱水
処理を行った。その後、十分湯水洗し、さらにカチオン
染料(Estrol Scarlet G)1%ow
f、浴のpH:3、浴比:1対100、95℃、45分
の染色を行い、洗浄後、シリコン系柔軟剤を付与して仕
上げた。これらの加工工程でのパイル抜けは殆ど認めら
れなかった。The flocked hair is dried at 120 ° C., 150
After curing at ℃, put it into the Wins dyeing machine. 0.1% NaOH and 0.2 g tripolyphosphoric acid as scouring aids
/ L and 2 g / l of a surfactant were added, and hot water treatment was performed at 90 ° C for 10 minutes. Then, wash with hot and cold water, and further add 1% of cationic dye (Estrol Scarlet G)
f, pH of bath: 3, bath ratio: 1: 100, dyeing at 95 ° C. for 45 minutes, washing, and then finishing with silicone softener. Almost no pile loss was observed in these processing steps.
【0025】得られた加工品は鮮やかな赤色を呈し、
0.19デニールの極細繊維のパイルが緻密にしっかり
と植毛された、手触り感の良好なビロード調のものであ
った。 実施例2〜3、比較例1〜3 実施例1に準じて、表1に示すように重合体の組み合わ
せで可細化性繊維を得て、電気植毛用パイル原糸の加工
評価を行なった。The obtained processed product has a bright red color,
A pile of 0.19 denier ultrafine fibers was densely and firmly planted, and had a velvety tone with a good feel. Examples 2 to 3 and Comparative Examples 1 to 3 According to Example 1, as shown in Table 1, a combination of polymers was used to obtain a thinnable fiber, and a processing evaluation of a pile raw yarn for electric flocking was performed. .
【0026】[0026]
【表1】 表1の各組成のパイル植毛品を実施例1に準じて加工
し、評価を行なった。[Table 1] The pile flocked products having the respective compositions shown in Table 1 were processed and evaluated according to Example 1.
【0027】実施例2、3は実施例1と同等の鮮明色豊
かな赤色を呈し、極細繊維特有の光沢と柔らかな手触り
を持つものであった。また、加工工程でのパイル抜けな
どの問題も何ら生じなかった。Examples 2 and 3 exhibited a bright red color similar to that of Example 1, and had the gloss and soft hand peculiar to the ultrafine fibers. In addition, there was no problem such as pile loss in the working process.
【0028】一方、比較例1、2はパイル植毛密度が緻
密にしっかりと植毛された手触り感の良好なものである
が、発色性に乏しく、商品価値のないものであった。さ
らに比較例3は発色性は良好であるが、パイルのへたり
が多いものであった。On the other hand, in Comparative Examples 1 and 2, the pile flocking density was densely and firmly flocked, and the touch was good, but the coloration was poor and the commercial value was low. Further, in Comparative Example 3, the color developability was good, but the pile pile was large.
【0029】実施例4 実施例1において、他の重合体としてナイロン6(28
0℃での溶融粘度:960ポイズ,軟化点:180℃)
を用い、その他は実施例1と同様にして紡糸、延伸を行
った。製糸性は良好であった。得られた延伸糸を電植用
パイル原糸として1.0mmにカットした。一方、ポリ
エステル系ポリウレタンの接着剤を塗布したナイロン6
の210デニール−30フィラメントを芯糸として、カ
ットパイルを電気植毛した(電圧3万V、電極間距離1
0cm)。パイルの飛翔性には何の問題もなく良好に植
毛を完了し、芯糸の周りに接着剤を介してパイルが植毛
された、いわゆるフロッキーヤーン(2500デニー
ル)を得た。Example 4 In Example 1, as another polymer, nylon 6 (28
Melt viscosity at 0 ° C: 960 poise, softening point: 180 ° C)
Was used and spinning and drawing were carried out in the same manner as in Example 1. The spinnability was good. The obtained drawn yarn was cut into 1.0 mm as a pile raw yarn for electroplantation. On the other hand, nylon 6 coated with polyester polyurethane adhesive
Of 210 denier-30 filament of No. 2 was used as the core yarn, and the cut pile was electro-implanted (voltage 30,000 V, distance between electrodes 1
0 cm). Flocking was completed satisfactorily without any problems with the flight properties of the pile, and a so-called flocky yarn (2500 denier) was obtained in which the pile was flocked around the core yarn with an adhesive.
【0030】次いで、このフロッキーヤーンを120℃
で乾燥し、カセ取りし、カセ染機に投入、精練助剤とし
てNaOH0.1%、トリポリリン酸0.2g/l、界
面活性剤2g/lをいれ90℃、10分の熱水処理を行
った。その後、十分湯水洗し、さらに酸性染料を投入9
0℃、45分の染色を行い、洗浄後、柔軟剤を付与して
仕上げた。これらの加工工程でのパイル抜けは殆ど認め
られなかった。Next, this flockey yarn was heated at 120 ° C.
Then, dry it with a scalpel, put it in a cassel dyeing machine, add 0.1% NaOH as a scouring aid, 0.2 g / l tripolyphosphoric acid, and 2 g / l surfactant, and perform hot water treatment at 90 ° C for 10 minutes. It was Then, rinse with hot water and add acid dye.
Dyeing was carried out at 0 ° C. for 45 minutes, and after washing, a softening agent was applied to finish. Almost no pile loss was observed in these processing steps.
【0031】この加工品は、極細繊維のフロッキーヤー
ンとして非常に特長のある光沢と柔らかなタッチをもつ
ものであった。また、熱水処理や染色仕上げなどの加工
をする前に織物や編物として、その後加工を施すことに
よって、高級感のあるインテリアのシートなどに最適で
ある。This processed product had a very characteristic gloss and soft touch as a flocky yarn of ultrafine fibers. Further, it is most suitable for interior seats with a high-class feeling by subjecting it to a woven fabric or a knitted fabric before being subjected to hot water treatment or dyeing finish, and then subjecting it to processing.
【0032】[0032]
【発明の効果】本発明のパイル原糸を用いた電気植毛品
は、有機溶剤や薬剤を使用することなく、かつ低い温度
で加工でき、次ぎの効果が得られる。 (1)特殊な加工装置も要らず、作業環境上の安全衛生
面の問題もなく、コスト的にも有利である。 (2)基布、接着剤、パイルなどを何ら損傷することな
く仕上げられる。このため、素材の脆化による風合いの
硬化や、パイルのへたりなく加工品をえることができ
る。 (3)得られる加工品は、極細パイルの緻密性、均一性
があって、極細繊維特有の光沢と良好な手触り感のもの
となり、内装材、シート材、高級衣料用などに好適であ
る。EFFECTS OF THE INVENTION An electric flocked product using the pile raw yarn of the present invention can be processed at a low temperature without using an organic solvent or a chemical agent, and the following effects can be obtained. (1) No special processing device is required, there is no safety and health problem in the working environment, and the cost is advantageous. (2) It can be finished without damaging the base cloth, the adhesive, the pile and the like. For this reason, it is possible to obtain a processed product without hardening the texture due to the embrittlement of the material and without sagging of the pile. (3) The obtained processed product has the fineness and homogeneity of the ultrafine pile, has the luster peculiar to the ultrafine fiber, and has a good feel to the touch, and is suitable for interior materials, sheet materials, high-grade clothing, and the like.
Claims (6)
あって、熱水溶解性重合体成分と、熱水に不溶解性でか
つ常圧可染性である他の重合体成分からなり、前記熱水
溶解性重合体成分の少なくとも一部が繊維表面を形成す
るように合流・複合された可細化性繊維であることを特
徴とする電気植毛用パイル原糸。1. A composite fiber comprising at least two components, which comprises a hot water-soluble polymer component and another polymer component which is insoluble in hot water and dyeable under atmospheric pressure. A pile raw yarn for electric flocking, characterized in that at least a part of a hot water-soluble polymer component is a thinnable fiber that is merged and composited so as to form a fiber surface.
成分比率が40重量%以下であって、可細化性繊維を実
質的に熱水で溶解処理し、熱水溶解性重合体を除去した
後の繊維の単糸繊度が0.5d以下であることを特徴と
する請求項1記載の電気植毛用パイル原糸。2. The proportion of the hot water-soluble polymer in the thinnable fiber is 40% by weight or less, and the thinnable fiber is substantially dissolved in hot water to obtain a hot water-soluble polymer. The pile yarn for electric flocking according to claim 1, wherein the single yarn fineness of the fibers after the coalescence is removed is 0.5 d or less.
成分であることを特徴とする請求項1または2記載の電
気植毛用パイル原糸。 A.主たる酸成分がテレフタル酸であって、他の酸成分
は8〜15mol%の5−ナトリウムスルホイソフタル
酸、および5〜40mol%のイソフタル酸であり、主
たるジオール成分がエチレングリコールよりなる共重合
ポリエステルである共重合ポリエステル。 B.主たる酸成分がテレフタル酸であって、他の酸成分
は1〜15mol%の5−ナトリウムスルホイソフタル
酸、および20mol%以下のイソフタル酸であり、主
たるジオール成分がエチレングリコールとビスフェノー
ルAのエチレンオキシド付加物よりなる共重合ポリエス
テル。3. The pile yarn for electric flocking according to claim 1, wherein the hot water-soluble polymer component is one of the following components. A. The main acid component is terephthalic acid, the other acid components are 8 to 15 mol% 5-sodium sulfoisophthalic acid, and 5 to 40 mol% isophthalic acid, and the main diol component is a copolyester composed of ethylene glycol. A copolyester. B. The main acid component is terephthalic acid, the other acid components are 1 to 15 mol% 5-sodium sulfoisophthalic acid, and 20 mol% or less isophthalic acid, and the main diol component is ethylene glycol adduct of bisphenol A with ethylene oxide. A copolyester consisting of.
ポリエステルであることを特徴とする請求項1〜3記載
のいずれか一項の電気植毛用パイル原糸。 A.テレフタル酸とエチレングリコールとを主たる構成
成分とし、全酸成分に対し1.5〜5.5mol%の5
−ナトリウムスルホイソフタル酸、および全ポリマーに
対し1〜10重量%のポリアルキレングリコールもしく
はその誘導体を含有する共重合ポリエステルである共重
合ポリエステル。4. The pile yarn for electric flock according to claim 1, wherein the other polymer component which is dyeable under atmospheric pressure is the following polyester. A. The main components are terephthalic acid and ethylene glycol, and 1.5 to 5.5 mol% of 5 with respect to all acid components.
A copolyester which is a copolyester containing sodium sulfoisophthalic acid and 1 to 10% by weight, based on the total polymer, of a polyalkylene glycol or a derivative thereof.
ミドである請求項1〜4記載のいずれか一項の電気植毛
用パイル原糸。5. The pile yarn for electro-implantation according to claim 1, wherein the other polymer component which is dyeable under atmospheric pressure is polyamide.
毛用パイル原糸からなるフロッキーヤーン。6. A flocky yarn comprising the pile yarn for electric flock according to any one of claims 1 to 5.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27544893A JPH07126919A (en) | 1993-11-04 | 1993-11-04 | Pile raw yarn for electric transplantation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27544893A JPH07126919A (en) | 1993-11-04 | 1993-11-04 | Pile raw yarn for electric transplantation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH07126919A true JPH07126919A (en) | 1995-05-16 |
Family
ID=17555674
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP27544893A Pending JPH07126919A (en) | 1993-11-04 | 1993-11-04 | Pile raw yarn for electric transplantation |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH07126919A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2017515991A (en) * | 2014-05-09 | 2017-06-15 | アルカンタラ、ソシエタ、ペル、アチオニAlcantara S.P.A. | Flocked material and its manufacturing process |
| JP2019131913A (en) * | 2018-01-30 | 2019-08-08 | Kbセーレン株式会社 | Composite fiber |
-
1993
- 1993-11-04 JP JP27544893A patent/JPH07126919A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2017515991A (en) * | 2014-05-09 | 2017-06-15 | アルカンタラ、ソシエタ、ペル、アチオニAlcantara S.P.A. | Flocked material and its manufacturing process |
| JP2019131913A (en) * | 2018-01-30 | 2019-08-08 | Kbセーレン株式会社 | Composite fiber |
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