JPH04289222A - Divisible conjugate fiber and fiber aggregate thereof - Google Patents
Divisible conjugate fiber and fiber aggregate thereofInfo
- Publication number
- JPH04289222A JPH04289222A JP5281491A JP5281491A JPH04289222A JP H04289222 A JPH04289222 A JP H04289222A JP 5281491 A JP5281491 A JP 5281491A JP 5281491 A JP5281491 A JP 5281491A JP H04289222 A JPH04289222 A JP H04289222A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- component
- fibers
- components
- present
- 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.)
- Granted
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 120
- 150000001875 compounds Chemical class 0.000 claims abstract description 22
- 238000002074 melt spinning Methods 0.000 claims abstract description 12
- 239000007791 liquid phase Substances 0.000 claims abstract description 10
- 239000002131 composite material Substances 0.000 claims description 29
- 239000000470 constituent Substances 0.000 claims description 21
- 229920005992 thermoplastic resin Polymers 0.000 claims description 14
- 229920001296 polysiloxane Polymers 0.000 claims description 11
- 238000002844 melting Methods 0.000 claims description 9
- 230000008018 melting Effects 0.000 claims description 9
- 229920000728 polyester Polymers 0.000 abstract description 21
- 229920000642 polymer Polymers 0.000 abstract description 14
- 229920002545 silicone oil Polymers 0.000 abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 14
- 239000004952 Polyamide Substances 0.000 abstract description 12
- 229920002647 polyamide Polymers 0.000 abstract description 12
- 238000009987 spinning Methods 0.000 abstract description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003607 modifier Substances 0.000 abstract 1
- 239000003921 oil Substances 0.000 abstract 1
- 229910052710 silicon Inorganic materials 0.000 abstract 1
- 239000010703 silicon Substances 0.000 abstract 1
- 229920000098 polyolefin Polymers 0.000 description 14
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 229920002292 Nylon 6 Polymers 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 229920000139 polyethylene terephthalate Polymers 0.000 description 8
- 239000005020 polyethylene terephthalate Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 238000004043 dyeing Methods 0.000 description 7
- 239000004744 fabric Substances 0.000 description 7
- 238000001914 filtration Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 229920001707 polybutylene terephthalate Polymers 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 239000012530 fluid Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 229920001155 polypropylene Polymers 0.000 description 5
- 229920001410 Microfiber Polymers 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000012770 industrial material Substances 0.000 description 4
- 239000004745 nonwoven fabric Substances 0.000 description 4
- 229920000299 Nylon 12 Polymers 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 229920001903 high density polyethylene Polymers 0.000 description 3
- 239000004700 high-density polyethylene Substances 0.000 description 3
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 3
- -1 polypropylene Polymers 0.000 description 3
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 2
- 229920000571 Nylon 11 Polymers 0.000 description 2
- 229920002302 Nylon 6,6 Polymers 0.000 description 2
- 229920000007 Nylon MXD6 Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- PYRZPBDTPRQYKG-UHFFFAOYSA-N cyclopentene-1-carboxylic acid Chemical compound OC(=O)C1=CCCC1 PYRZPBDTPRQYKG-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- UNILWMWFPHPYOR-KXEYIPSPSA-M 1-[6-[2-[3-[3-[3-[2-[2-[3-[[2-[2-[[(2r)-1-[[2-[[(2r)-1-[3-[2-[2-[3-[[2-(2-amino-2-oxoethoxy)acetyl]amino]propoxy]ethoxy]ethoxy]propylamino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-[(2r)-2,3-di(hexadecanoyloxy)propyl]sulfanyl-1-oxopropan-2-yl Chemical compound O=C1C(SCCC(=O)NCCCOCCOCCOCCCNC(=O)COCC(=O)N[C@@H](CSC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)C(=O)NCC(=O)N[C@H](CO)C(=O)NCCCOCCOCCOCCCNC(=O)COCC(N)=O)CC(=O)N1CCNC(=O)CCCCCN\1C2=CC=C(S([O-])(=O)=O)C=C2CC/1=C/C=C/C=C/C1=[N+](CC)C2=CC=C(S([O-])(=O)=O)C=C2C1 UNILWMWFPHPYOR-KXEYIPSPSA-M 0.000 description 1
- 101100382321 Caenorhabditis elegans cal-1 gene Proteins 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 239000011116 polymethylpentene Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Artificial Filaments (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Multicomponent Fibers (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
- Nonwoven Fabrics (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、圧力水などの圧力流体
の物理的衝撃処理によって分割が容易な複合繊維及びそ
の集合物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to composite fibers and aggregates thereof that can be easily split by physical impact treatment using a pressure fluid such as pressurized water.
【0002】0002
【従来の技術】同じ種類の素材、特にポリエステルまた
はポリオレフィンからなる繊維断面が異形の極細繊維は
、粒子の濾過効果が高く、濾過布、エアーフィルター、
抄紙用カンバスなど化学特性の均一性も必要とする濾過
用途の産業資材などに展開することが期待されている。[Prior Art] Ultrafine fibers made of the same type of material, especially polyester or polyolefin, with irregularly shaped fiber cross sections have a high particle filtration effect, and are used in filter cloth, air filters, etc.
It is expected that this material will be used in industrial materials for filtration applications, such as canvas for paper making, which also require uniform chemical properties.
【0003】従来、化学特性の均一性がある、すなわち
同じ素材でなる極細繊維は海島繊維の海成分を溶出させ
島成分からなる極細繊維のみで、該繊維は円形断面であ
り、また海成分を溶出除去するため非経済的で資源の浪
費が極めて大きく、これらを解決するため化学特性は不
均一であるが、すなわち2種の異なる素材を用いた分割
性複合繊維より作られる異形断面の極細繊維が開発され
た。[0003] Conventionally, ultrafine fibers with uniform chemical properties, that is, made of the same material, are only ultrafine fibers made of island components by eluting the sea components of sea-island fibers. The process of elution and removal is uneconomical and wastes a large amount of resources.In order to solve these problems, we have developed ultrafine fibers with irregular cross sections that are made from splittable composite fibers using two different materials, although their chemical properties are non-uniform. was developed.
【0004】従来、細デニール繊維を得る方法として分
割性のある複合繊維を利用することが知られている。例
えば特公昭53−47414号、特公昭53−4741
6号、特公昭63−14098号及び特開昭62−13
3164号各公報などで提案されている。Conventionally, it has been known to utilize splittable conjugate fibers as a method for obtaining fine denier fibers. For example, Special Publication No. 53-47414, Special Publication No. 53-4741
No. 6, JP 63-14098 and JP 62-13
It has been proposed in various publications such as No. 3164.
【0005】[0005]
【発明が解決しようとする課題】しかし、前記公報など
で開示された複合繊維は、いずれも異なる種類のポリマ
ーを構成単位として組み合わせたものである。[Problems to be Solved by the Invention] However, the composite fibers disclosed in the above-mentioned publications are all combinations of different types of polymers as constituent units.
【0006】例えばポリエステルとポリオレフィン、ポ
リエステルとポリアミド、ポリアミドとポリオレフィン
という組み合わせである。このような成分が1本の繊維
に組み合わせられて複合繊維になっているので、これを
分割し細デニールの繊維を得たときは当然のことながら
異種のポリマーからなる繊維が混在しており、この繊維
を原料とする製品は耐酸、耐アルカリ性、耐溶剤性、耐
湿熱性などの耐薬品性、融点、軟化点、熱分解温度、実
用上の最大使用可能温度などの熱特性、適合染料の種類
、染着度合いなどの染色性など各成分固有の化学特性を
混在して持っているのである。単なる粒子の濾過特性は
どの組み合わせの分割性複合繊維を用いても従来の円断
面を持つ繊維からなる濾過布よりも良い結果をいずれも
示すが、構成素材に耐薬品性の均一性が要求される濾過
布、抄紙用カンバスなどの濾過用産業資材では、従来の
分割性複合繊維、例えばポリエステル/ポリアミドの組
み合わせの繊維では実用できない場合が極めて多く、使
用上同一種の組み合わせの分割性複合繊維、特にポリエ
ステル/ポリエステルの組み合わせの分割性複合繊維の
実現が望まれていたが、ポリエステル同士の相溶性が大
きく(場合によっては界面で共重合反応を起こす)実用
的には製造することができなかったという課題がある。Examples include combinations of polyester and polyolefin, polyester and polyamide, and polyamide and polyolefin. These components are combined into a single fiber to make a composite fiber, so when this is divided to obtain fine denier fibers, it is natural that fibers made of different types of polymers are mixed together. Products made from this fiber have chemical resistance such as acid resistance, alkali resistance, solvent resistance, and moist heat resistance, thermal properties such as melting point, softening point, thermal decomposition temperature, maximum practical usable temperature, and types of compatible dyes. Each component has a mixture of chemical properties unique to it, such as dyeing properties such as the degree of dyeing. Regarding the filtration properties of simple particles, no matter which combination of splittable conjugate fibers is used, they all show better results than conventional filter cloths made of fibers with a circular cross section, but the constituent materials must have uniform chemical resistance. For industrial materials for filtration such as filter cloth and canvas for papermaking, conventional splittable conjugate fibers, such as polyester/polyamide combination fibers, are often not practical. In particular, it was desired to realize a splittable conjugate fiber made from a polyester/polyester combination, but the polyesters were highly compatible with each other (in some cases, a copolymerization reaction occurred at the interface), making it impractical to manufacture. There is a problem.
【0007】また本発明者がすでに提案しているポリプ
ロピレン(PP)/高密度ポリエチレン(HDPE)等
のポリオレフィン/ポリオレフィンの組み合わせ、ある
いはナイロン−6(NY6)/ナイロン−12(NY1
2)あるいはMXD6ナイロン(MXD6)/ナイロン
−6(NY6)等のポリアミド/ポリアミドの組み合わ
せからなる分割性複合繊維は、従来のポリエステル/ポ
リアミドあるいはポリエステル/ポリオレフィンの組み
合わせの分割性複合繊維よりも分割性に劣るため、生産
上分割性の向上が要求されている。In addition, combinations of polyolefins/polyolefins such as polypropylene (PP)/high-density polyethylene (HDPE), or nylon-6 (NY6)/nylon-12 (NY1), which the present inventor has already proposed, may also be used.
2) Alternatively, splittable conjugate fibers made of a polyamide/polyamide combination such as MXD6 nylon (MXD6)/nylon-6 (NY6) are more splittable than conventional splittable conjugate fibers made of polyester/polyamide or polyester/polyolefin combinations. Therefore, improvements in divisibility are required for production purposes.
【0008】なお、従来の市販されている分割性複合繊
維は構成成分が異質の熱可塑性樹脂の組み合わせからな
る繊維のため、各成分は同一種の染料で同時に染色する
ことが不可能であり、生産上、経済上の問題もあった。[0008] Conventional commercially available splittable composite fibers are fibers made of a combination of different thermoplastic resin components, so it is impossible to dye each component simultaneously with the same type of dye. There were also production and economic problems.
【0009】本発明は、前記従来技術の課題を解決する
ため、圧力水などの圧力流体の物理的衝撃処理によって
分割が容易な複合繊維及びその集合物を提供する。[0009] In order to solve the problems of the prior art, the present invention provides composite fibers and aggregates thereof that can be easily split by physical impact treatment with a pressure fluid such as pressure water.
【0010】0010
【課題を解決するための手段】前記目的を達成するため
、本発明の分割性複合繊維は、融点(Tm℃)が100
<Tm<350の範囲の熱可塑性樹脂からなる第1成分
と第2成分で少なくとも構成された複合繊維において、
溶融紡糸温度で液相となる耐熱性化合物が第1成分と第
2成分の間の界面の少なくとも一部に存在し、繊維断面
方向から見て前記複数成分のうち少なくとも1成分が2
個以上に分割されており、各成分は各々が繊維断面の構
成単位となっており、各構成単位は互に異なる成分の構
成単位と隣接し、かつ実質的に大部分の各構成単位はそ
の一部を繊維表面に露出していることを特徴とする。[Means for Solving the Problems] In order to achieve the above object, the splittable conjugate fiber of the present invention has a melting point (Tm°C) of 100
A composite fiber comprising at least a first component and a second component made of a thermoplastic resin in the range of <Tm<350,
A heat-resistant compound that becomes a liquid phase at the melt spinning temperature is present at least in a part of the interface between the first component and the second component, and at least one of the plurality of components is
Each component is a constituent unit of the fiber cross section, each constituent unit is adjacent to a constituent unit of a different component, and substantially most of each constituent unit is a constituent unit of the fiber cross section. It is characterized by a portion being exposed on the fiber surface.
【0011】前記構成においては、溶融紡糸温度で液相
となる耐熱性化合物がオルガノポリシロキサンおよびこ
れらの変性体であることが好ましい。[0011] In the above structure, it is preferable that the heat-resistant compound that becomes a liquid phase at the melt spinning temperature is an organopolysiloxane or a modified product thereof.
【0012】また本発明の繊維集合物は、前記分割性複
合繊維が少なくとも30重量%含まれており、かつ前記
複合繊維が分割されてなるという構成を備えたものであ
る。Furthermore, the fiber aggregate of the present invention contains at least 30% by weight of the splittable conjugate fibers, and has a structure in which the conjugate fibers are split.
【0013】[0013]
【作用】前記本発明の構成によれば、溶融紡糸温度で液
相となる耐熱性化合物が第1成分と第2成分の間の界面
の少なくとも一部に存在し、繊維断面方向から見て前記
複数成分のうち少なくとも1成分が2個以上に分割され
ており、各成分は各々が繊維断面の構成単位となってお
り、各構成単位は互に異なる成分の構成単位と隣接し、
かつ実質的に大部分の各構成単位はその一部を繊維表面
に露出しているので、圧力水などの圧力流体の物理的衝
撃処理によって分割が容易な複合繊維及びその集合物と
することができる。また複合繊維の構成成分であるポリ
マの種類を問わずに分割できる。[Function] According to the configuration of the present invention, the heat-resistant compound that becomes a liquid phase at the melt spinning temperature exists at least in a part of the interface between the first component and the second component, and At least one component among the plurality of components is divided into two or more, each component is a constituent unit of the fiber cross section, and each constituent unit is adjacent to a constituent unit of a different component,
In addition, since most of the constituent units are partially exposed on the fiber surface, it is possible to form composite fibers and aggregates thereof that can be easily divided by physical impact treatment with pressure fluid such as pressurized water. can. Furthermore, it can be divided regardless of the type of polymer that is a component of the composite fiber.
【0014】また、溶融紡糸温度で液相となる耐熱性化
合物がオルガノポリシロキサンおよびこれらの変性体で
あるという本発明の好ましい構成によれば、さらに分割
が容易となる。Further, according to a preferred configuration of the present invention in which the heat-resistant compound that becomes a liquid phase at the melt spinning temperature is an organopolysiloxane or a modified product thereof, division becomes even easier.
【0015】また、本発明の繊維集合物の構成によれば
、極細の分割繊維を含み、絡合一体性にも優れているの
で、濾過布、抄紙用カンバスなどの濾過用産業資材など
に有用なものとすることができる。Furthermore, according to the structure of the fiber aggregate of the present invention, it contains ultra-fine split fibers and has excellent entangled integrity, so it is useful for industrial materials for filtration such as filter cloth and papermaking canvas. It can be made into something.
【0016】[0016]
【実施例】以下実施例を用いて本発明をさらに具体的に
説明する。なお以下の実施例において、単に%と表示し
ているのは重量%を意味する。本発明に用いる熱可塑性
樹脂は、用途を考えると第1成分と第2成分ともにポリ
エステル類、ポリアミド類、ポリオレフィン類等の同一
種類のポリマーが好ましく、全く同一のポリマーであっ
ても良いが、実用生産を考えると同一種類であっても溶
融表面張力(γ;dyne/cm at265℃)ある
いは溶解パラメータ値(SP値δ:Cal1/2 cm
3/2 )に差の大きい種類のポリマーの組み合わせが
より好ましい。例えばポリエステル/ポリエステルの組
み合わせであるポリエチレンテレフタレート(PET)
/ポリブチレンテレフタレート(PBT)、ポリオレフ
ィン/ポリオレフィンの組み合わせであるPP/HDP
Eあるいはポリアミドの組み合わせであるNY6/NY
12、MXD6/NY6の組み合わせであるが、特にこ
れに限定はしない。EXAMPLES The present invention will be explained in more detail below using examples. In addition, in the following examples, simply expressed as % means weight %. Considering the use of the thermoplastic resin used in the present invention, both the first component and the second component are preferably the same type of polymer such as polyesters, polyamides, polyolefins, etc., and may be completely the same polymer, but in practical use Considering production, even if the type is the same, the melting surface tension (γ; dyne/cm at 265°C) or the solubility parameter value (SP value δ: Cal1/2 cm
A combination of polymers with a large difference in the ratio of 3/2) is more preferable. For example, polyethylene terephthalate (PET), which is a combination of polyester/polyester
/Polybutylene terephthalate (PBT), polyolefin/PP/HDP which is a combination of polyolefin
NY6/NY which is a combination of E or polyamide
12. It is a combination of MXD6/NY6, but is not particularly limited to this.
【0017】また従来は分割繊維としては全く考えられ
なかった組み合わせのPET/PETなどの組み合わせ
でも、分割可能である。用いることのできる熱可塑性樹
脂は、融点が100〜350℃の樹脂を用いることが可
能だが組み合わせの都合上融点が100〜300℃の樹
脂が好ましく、用いる両成分を区分する化合物の熱分解
などを考慮すると紡糸温度(T℃)を300℃以下にす
ることが好ましいため、融点が100〜270℃の樹脂
が最も好ましく、融点が100℃未満の樹脂は、繊維製
造の時延伸条件等の制限を生じやすく好ましくない。用
いることのできる熱可塑性樹脂は、PET、PBTなど
のポリエステル類(T)、ナイロン−6(NY6)、ナ
イロン−66(NY66)、ナイロン−6,10(NY
610)、ナイロン−11(NY11)、ナイロン−1
2(NY12)、MXD6ナイロン(MXD6)などの
ポリアミド類(NY)およびPP、PE、ポリメチルペ
ンテン(PMP)、エチレン共重合体、プロピレン共重
合体などのポリオレフィン類(O)のホモポリマー、コ
ポリマーおよび変性体が好ましく、ポリカーボネート、
ポリスチレンなどの融点が100〜350℃の熱可塑性
樹脂を用いることができる。Furthermore, even combinations such as PET/PET, which have never been considered as split fibers, can be split. As the thermoplastic resin that can be used, it is possible to use a resin with a melting point of 100 to 350°C, but for convenience of combination, a resin with a melting point of 100 to 300°C is preferable. Taking this into consideration, it is preferable to keep the spinning temperature (T°C) below 300°C, so a resin with a melting point of 100 to 270°C is most preferable, and resins with a melting point of less than 100°C are subject to restrictions such as stretching conditions during fiber production. It is easy to occur and is not desirable. Thermoplastic resins that can be used include polyesters (T) such as PET and PBT, nylon-6 (NY6), nylon-66 (NY66), and nylon-6,10 (NY
610), nylon-11 (NY11), nylon-1
Homopolymers and copolymers of polyamides (NY) such as 2 (NY12) and MXD6 nylon (MXD6), and polyolefins (O) such as PP, PE, polymethylpentene (PMP), ethylene copolymers, and propylene copolymers. and modified products are preferred, polycarbonate,
A thermoplastic resin having a melting point of 100 to 350°C, such as polystyrene, can be used.
【0018】本発明に用いる化合物は、いずれか一方の
熱可塑性樹脂に混練りして繊維に導入する方法と、3成
分複合繊維の手法を用い、第1成分と第2成分を該化合
物を介して接する繊維断面構造に配置する方法の2つの
方法によって本発明の分割性複合繊維に導入することが
できる。前者に用いる化合物は、両成分に非相溶で、溶
融紡糸時は液状でかつ溶融紡糸時にガス化もしくはガス
状物を生じ溶融状態の繊維を発泡状態としない様に沸点
もしくは熱分解してガスを発生開始する温度(TB ℃
)が好ましくは溶融紡糸温度(T℃)より20℃以上高
く、溶融紡糸温度で、両成分より金属に対する濡れ性(
親和性)が良い化合物が好ましく、より好ましくは常温
で液状で、分割処理後容易に除去可能な化合物である。
現在本発明の効果を確認している具体例は、ジメチルポ
リシロキサン、ジフェニルポリシロキサンなどのシリコ
ンオイル(以下SiOという)と、ポリメチル水素シロ
キサンのアルケン(C10〜C50)およびプロピレン
付加物(以下NR−Bという)などのオルガノポリシロ
キサン(OS)およびこれらの変性体、付加体であるが
、これに限定されるものではない。[0018] The compound used in the present invention is kneaded into one of the thermoplastic resins and introduced into the fiber, and the first component and the second component are introduced through the compound using a method for three-component composite fibers. It can be introduced into the splittable conjugate fiber of the present invention by two methods: arranging it in the fiber cross-sectional structure in contact with each other. The compound used for the former is incompatible with both components, is liquid during melt spinning, and has a boiling point or thermal decomposition to gas so as not to gasify or produce a gaseous substance during melt spinning and cause the molten fiber to become foamed. Temperature at which temperature starts to occur (TB ℃
) is preferably 20°C or more higher than the melt spinning temperature (T°C), and the wettability (
Compounds with good affinity) are preferred, and compounds that are liquid at room temperature and easily removable after splitting are more preferred. Specific examples for which the effects of the present invention have been confirmed at present include silicone oils (hereinafter referred to as SiO) such as dimethylpolysiloxane and diphenylpolysiloxane, and alkene (C10 to C50) and propylene adducts of polymethylhydrogensiloxane (hereinafter referred to as NR- These include, but are not limited to, organopolysiloxanes (OS) such as B) and modified products and adducts thereof.
【0019】シリコンオイルを用いPET/PBTの分
割性複合繊維を得る場合は、たとえば1μm以下の粒径
でシリコンオイルを5重量%以上練り込んだペレットを
溶融し、図2に示すような紡糸口金部において溶融樹脂
の流れに11の垂直方向から流し、12の流れに平行な
方向から流入する他の成分と合流させて断面が図1(c
)の形の繊維とする。When using silicone oil to obtain splittable conjugate fibers of PET/PBT, for example, pellets with a particle size of 1 μm or less and 5% by weight or more of silicone oil kneaded are melted and prepared using a spinneret as shown in FIG. At the section, the molten resin flows from a direction perpendicular to the flow of molten resin 11, and is merged with other components flowing from a direction parallel to the flow of 12, so that the cross section becomes as shown in Fig. 1(c).
) in the form of fibers.
【0020】垂直方向の溶融樹脂の流路11は、金属と
の接触面積が大きく取ってあり、シリコンオイルの液滴
が凝縮し、該金属面を濡し、該流路の排出口から出る樹
脂成分は、少なくとも一部がシリコンオイルでおおわれ
た状態で他の成分と合流するため両成分はシリコンオイ
ルを介して接する繊維断面を形成するのである。なお、
シリコンオイルで完全に両成分が区分されてしまうと延
伸時バラバラになるのでステープルとして用いる場合は
、不完全区分が好ましい。The vertical molten resin flow path 11 has a large contact area with the metal, and droplets of silicone oil condense and wet the metal surface, causing the resin to exit from the outlet of the flow path. Since each component joins with another component while being at least partially covered with silicone oil, both components form a fiber cross section in which they are in contact with each other via the silicone oil. In addition,
If both components are completely separated by silicone oil, they will fall apart during stretching, so when used as a staple, incomplete separation is preferred.
【0021】本発明に用いる後者の方法は、例えば図2
に示す紡糸口金を用いる場合、図3のように本発明に用
いる紡糸温度で液相となる化合物の海13(シリコンオ
イルを微分散したポリマ又はシリコンオイル若しくはシ
リコン変性体でもよい)に、他のポリマ成分12を流下
させ、図4の様に本発明に用いる化合物13でおおわれ
た状態の成分とし、他の成分と合流させて両成分が本発
明に用いる化合物を介して接する繊維断面を形成させる
のである。本発明に用いる化合物は上記前者の方法の例
に用いたものの他に、両成分と非相溶な熱可塑性樹脂も
用いることが可能であるが、本発明の分割性複合繊維を
分割処理後、該化合物の除去が容易な場合もしくは除去
不要の用途を除き従来の分割性繊維と同様な欠点を生じ
るので好ましくない。The latter method used in the present invention is illustrated in FIG.
When using the spinneret shown in FIG. 3, other compounds are added to the sea 13 of the compound (which may be a polymer in which silicone oil is finely dispersed, silicone oil, or a modified silicone) that becomes a liquid phase at the spinning temperature used in the present invention, as shown in FIG. The polymer component 12 is allowed to flow down to form a component covered with the compound 13 used in the present invention as shown in FIG. 4, and is merged with other components to form a fiber cross section where both components are in contact via the compound used in the present invention. It is. In addition to the compounds used in the former method example above, thermoplastic resins that are incompatible with both components can also be used as the compound used in the present invention, but after the splittable composite fiber of the present invention is split, Unless the compound is easy to remove or for applications where removal is unnecessary, it is not preferred because it causes the same drawbacks as conventional splittable fibers.
【0022】本発明の分割性複合繊維の繊維断面は図1
(a)〜(e)に示す様な2成分の内少なくとも1成分
が2個以上に分割され、各成分は各々が繊維断面の構成
単位となっており、各構成単位は互に異なる成分の構成
単位と隣接し、且つその一部を繊維表面に露出している
構造であり、両成分の容積比は30/70〜70/30
の範囲にあるのが好ましい。なお、本発明において「実
質的に大部分の各構成単位はその一部を繊維表面に露出
している」という意味は、ウォータージェット等の流体
による物理的衝撃処理によって分割できる程度に各構成
単位が繊維表面に露出していればよいことを意味する。
したがって、例えば繊維内部に幾らかの構成成分が存在
していても良いし、製造上の都合から繊維全体がある一
つの構成成分によって薄く被覆されている状態であって
も良い。The fiber cross section of the splittable conjugate fiber of the present invention is shown in FIG.
At least one of the two components shown in (a) to (e) is divided into two or more parts, each component is a constituent unit of the fiber cross section, and each constituent unit is composed of different components. It has a structure that is adjacent to the structural unit and a part of it is exposed on the fiber surface, and the volume ratio of both components is 30/70 to 70/30.
It is preferable that it is in the range of . In addition, in the present invention, "substantially most of each structural unit has a part exposed on the fiber surface" means that each structural unit is separated to the extent that it can be divided by physical impact treatment with a fluid such as a water jet. This means that it is sufficient if it is exposed on the fiber surface. Therefore, for example, some constituent components may be present inside the fiber, or the entire fiber may be thinly coated with one constituent component for manufacturing reasons.
【0023】本発明の分割性複合繊維は0.5〜100
デニールの繊度の繊維であり、マルチフィラメント、ス
テープルおよび紙用短カットなどの少なくとも2倍に延
伸された繊維形態が好ましく、スタフィングボックスな
どの物理的折りたたみ方式の捲縮付与あるいは打梳綿機
を用いるなど物理的な繊維分割促進処理を施した後、さ
らウォータージェット装置などの物理的衝撃発生装置を
用いて分割処理して細繊度繊維に分割できる。[0023] The splittable conjugate fiber of the present invention has a molecular weight of 0.5 to 100
denier fineness, preferably in fiber forms that are at least twice as drawn, such as multifilament, staple, and paper cut, and are crimped by physical folding methods such as stuffing boxes, or by carding machines. After performing a physical fiber splitting promotion treatment such as using a water jet device, the fiber can be further divided into fine fibers by a dividing treatment using a physical impact generating device such as a water jet device.
【0024】本発明の分割性複合繊維はポリエステル、
アクリル、ナイロン、レーヨンなどの他の繊維もしくは
ポルプ合成パルプなどの繊維状物と混綿混合および/ま
たは層状に重ねた繊維集合物として用いることが出来、
該複合繊維の分割処理は、混用前もしくは混用後のいず
れであってもよい。該繊維集合物とは、フェルト、不織
布、紙、紡績糸とその織編物、フロッキー加工品および
マルチフィラメントとその織編物など繊維加工品をいい
、該繊維集合物中に該複合繊維は少なくとも部分的には
分割された状態で含まれ、保水性保湿性に効果的な微細
繊維もしくはふき取り性に優れた繊維断面にシャープな
角を持つ繊維として存在する。これらの効果を有効に発
揮するには本発明の複合繊維を少なくとも30重量%含
むのが好ましい。The splittable conjugate fiber of the present invention is polyester,
It can be used as a fiber aggregate mixed and/or layered with other fibers such as acrylic, nylon, and rayon or fibrous materials such as polp synthetic pulp.
The splitting treatment of the composite fibers may be performed either before or after mixing. The fiber aggregate refers to fiber processed products such as felt, nonwoven fabric, paper, spun yarn and its woven or knitted fabric, flocked products, multifilament and its woven or knitted fabric, and the composite fiber is at least partially contained in the fiber aggregate. It is contained in a divided state and exists as fine fibers that are effective for water retention and moisture retention, or as fibers with sharp corners in the fiber cross section that are easy to wipe off. In order to effectively exhibit these effects, it is preferable to contain at least 30% by weight of the composite fiber of the present invention.
【0025】本発明の複合繊維はポリエステル/ポリエ
ステル、ポリオレフィン/ポリオレフィンおよびポリア
ミド/ポリアミドの様な同一種類の熱可塑性樹脂の組み
合わせの分割性複合繊維を含み、これらは従来の分割性
繊維としては考えられなかった成分同士の組み合わせも
分割可能とした。さらに全く同一の熱可塑性樹脂の組み
合わせ、例えばPET/PETも分割できる可能性があ
り、この手法では、用いる両成分分離用化合物の耐熱性
と、両成分の耐熱性に制限を受けるのみでほとんどあら
ゆる熱可塑性樹脂の組み合わせでも分割性を有する分割
性複合繊維とできると推定される。The composite fibers of the present invention include splittable composite fibers of combinations of thermoplastic resins of the same type, such as polyester/polyester, polyolefin/polyolefin, and polyamide/polyamide, which are not considered conventional splittable fibers. It is now possible to divide combinations of ingredients that were not previously available. Furthermore, it is possible to separate a combination of identical thermoplastic resins, such as PET/PET, and this method is limited only by the heat resistance of the compound used to separate the two components and the heat resistance of both components. It is presumed that a combination of thermoplastic resins can also be used to create a splittable conjugate fiber.
【0026】特に一般濾過材の分野で極めて広く使用さ
れているポリエステル繊維に替え、ポリエステル/ポリ
エステルの組み合わせの分割性複合繊維を分割して微細
繊維として用いると従来と同じ使用条件下で、今までよ
りもさらに細かい粒子を捕集することが可能となり、極
めて有用である。また、耐熱性はあまり要求されない分
野で耐酸、耐アルカリ性の両方が要求される濾過材には
PP/HDPEの組み合わせの分割性複合繊維を本発明
を適用しない場合よりはるかに容易に分割可能とでき有
用である。In place of polyester fibers, which are extremely widely used in the field of general filtration media in particular, if splittable composite fibers of a combination of polyester/polyester are split and used as fine fibers, under the same usage conditions as before, This makes it possible to collect even finer particles than the conventional method, making it extremely useful. In addition, for filter media that requires both acid resistance and alkali resistance in fields where heat resistance is not so required, splittable composite fibers of a combination of PP/HDPE can be made much easier to split than when the present invention is not applied. Useful.
【0027】また第3成分として用いる本発明に用いる
化合物をオルガノポリシロキサンとすると繊維中に残留
してもこれは耐熱、耐酸、アルカリ性と無毒性に優れて
いるため、用途上の制限が少なく都合が良い。以下具体
的実験例を説明する。Furthermore, when the compound used in the present invention used as the third component is organopolysiloxane, even if it remains in the fiber, it has excellent heat resistance, acid resistance, alkalinity, and non-toxicity, so there are few restrictions on the use and it is convenient. is good. A specific experimental example will be explained below.
【0028】実施例1〜7、比較例1〜5表1〜2に示
す様に種々熱可塑性樹脂の組み合わせのものを図1(c
)に示すような風車状に配列した断面を持つ複合繊維と
して溶融紡糸して未延伸糸とした。両成分の容積比率は
50:50で、両成分は互いに相手成分によって8分割
されている。各成分間の界面は透過型光学顕微鏡で未延
伸糸の繊維断面を拡大観察し界面の有無を判定した。オ
ルガノポリシロキサンは、第1成分に添加、色相類似の
成分の組み合わせの場合は第2成分に淡く原料着色マス
ターバッチを添加した。紡糸した未延伸糸を95℃熱水
中で延伸、繊維処理剤を含浸しながらスタッファボック
スを通して機械捲縮を与え、110℃のネットコンベア
式熱風貫通型乾燥機で15分間乾燥し、45mmに切断
してステープル繊維とした。Examples 1 to 7, Comparative Examples 1 to 5 As shown in Tables 1 to 2, various combinations of thermoplastic resins were used in Figure 1(c).
) A composite fiber with a pinwheel-shaped cross section was melt-spun into an undrawn yarn. The volume ratio of both components is 50:50, and both components are divided into eight parts by the other component. The presence or absence of an interface between each component was determined by magnifying the fiber cross section of the undrawn yarn using a transmission optical microscope. The organopolysiloxane was added to the first component, and in the case of a combination of components with similar hues, a raw material coloring masterbatch was added lightly to the second component. The spun undrawn yarn was drawn in hot water at 95°C, mechanically crimped through a stuffer box while impregnated with a fiber treatment agent, and dried for 15 minutes in a net conveyor type hot air dryer at 110°C to a length of 45 mm. It was cut into staple fibers.
【0029】このステープルファイバーをローラーカー
ドで90g/m2目付のウェブとした後、100〜17
0Kg/cm2 の圧力水で5秒間処理し複合繊維が分
割するか否かを評価したさらに下記条件で染色を実施し
た。After forming this staple fiber into a web with a fabric weight of 90 g/m2 using a roller card,
The composite fibers were treated with water under a pressure of 0 kg/cm2 for 5 seconds to evaluate whether or not they would split.Furthermore, dyeing was carried out under the following conditions.
【0030】A.分割率
分割性複合繊維100本中の分割した繊維の本数をいい
、%で表わす。A. Split ratio refers to the number of split fibers out of 100 split conjugate fibers and is expressed in %.
【0031】B.染色条件および評価 評価 ◎:濃色に染色できた。 ○:やや淡く染色できた。 △:片成分だけ染色できた。 ×:染色できず。B. Staining conditions and evaluation evaluation ◎: Dyeing was possible in a deep color. ○: Slightly light dyeing was possible. △: Only one component could be dyed. ×: Unable to dye.
【0032】a)分散染料の場合
カヤロンポリエスターRed BR−S;1g/l 、
テキサトンTHS−100;0.3g/lおよび硫酸ア
ンモニウム200g/lと酢酸3.3ml/l のPH
調整液10ml/lからなる染色液中に浴比1:30で
浸漬し130℃で30分間高圧染色し、ソーダ灰;2g
/lおよびハイドロサルファイト;2g/lを含む80
℃の浴中で5分間処理した後乾燥して染色物とした。a) In the case of disperse dye Kayalon Polyester Red BR-S; 1 g/l,
Texaton THS-100; pH of 0.3 g/l and ammonium sulfate 200 g/l and acetic acid 3.3 ml/l
It was immersed in a dye solution consisting of a conditioning solution of 10 ml/l at a bath ratio of 1:30 and subjected to high-pressure dyeing at 130°C for 30 minutes, followed by 2 g of soda ash.
/l and hydrosulfite; 80 containing 2g/l
It was treated in a bath at 0.degree. C. for 5 minutes and then dried to give a dyed product.
【0033】b)酸性染料の場合
住友化学ソーラピュアーブルーAFX1g/lおよび染
色助剤として無水硫酸ナトリウム;3.3g/l、酢酸
0.7g/lを用い浴比1:30で1時間煮沸して染色
、乾燥して染色物とした。b) In the case of acid dyes Sumitomo Chemical Solar Pure Blue AFX 1 g/l, anhydrous sodium sulfate; 3.3 g/l and acetic acid 0.7 g/l as dyeing aids were used and boiled for 1 hour at a bath ratio of 1:30. It was dyed and dried to make a dyed product.
【0034】実施例8
比較例2の組み合わせで紡糸口金部PBT側の溶融樹脂
流路に実施例1より粘度の高いシリコンオイルを充満さ
せた後、比較例2と同様にして複合繊維を溶融紡糸し、
シリコンオイル量がPBT重量に対し5%程度の未延伸
糸を採取し、実施例2と同様にして処理した。繊維断面
は実施例2より明確であり、170Kg/cm2 の圧
力水で5秒間処理したものは分割率20%であった。Example 8 After filling the molten resin channel on the PBT side of the spinneret with silicone oil having a higher viscosity than in Example 1 using the combination of Comparative Example 2, composite fibers were melt-spun in the same manner as in Comparative Example 2. death,
An undrawn yarn in which the amount of silicone oil was about 5% based on the weight of PBT was collected and treated in the same manner as in Example 2. The fiber cross section was clearer than in Example 2, and the split ratio of the fiber treated with 170 kg/cm2 pressure water for 5 seconds was 20%.
【0035】以上の条件及び結果を表1〜2に示す。The above conditions and results are shown in Tables 1 and 2.
【0036】[0036]
【表1】[Table 1]
【0037】[0037]
【表2】[Table 2]
【0038】以上説明した通り、本実施例の分割性複合
繊維は、従来難分解もしくは分割不可能と考えられてい
た同一種類の熱可塑性樹脂の組み合わせであり、これら
を分割可能とした。特にポリエステル/ポリエステルの
組み合わせの繊維は従来品より微細粒子まで捕集可能な
ため産業用フィルター分野で好都合であり、化学的に不
活性なためメディカル不織布、あるいは耐酸と耐アルカ
リ性の両方が要求されるポリオレフィン/ポリオレフィ
ンの組み合わせの繊維を容易に分割処理可能とすること
ができた。また前記のようにして得られた不織布は、分
割繊維の絡み合いが良く、フェルト状に一体化している
ものであった。またポリマ中に微分散されたシリコンオ
イルの存在により、不織布は撥水性に優れたものであっ
た。As explained above, the splittable conjugate fiber of this example is a combination of thermoplastic resins of the same type, which were conventionally thought to be difficult to decompose or cannot be split, and can be split. In particular, polyester/polyester combination fibers are advantageous in the field of industrial filters because they can collect even finer particles than conventional products, and because they are chemically inert, they are required to be used as medical nonwoven fabrics or to have both acid and alkali resistance. It was possible to easily split the polyolefin/polyolefin combination fiber. In addition, the nonwoven fabric obtained as described above had good intertwining of the split fibers and was integrated into a felt-like structure. Furthermore, due to the presence of silicone oil finely dispersed in the polymer, the nonwoven fabric had excellent water repellency.
【0039】[0039]
【発明の効果】以上説明した通り、本発明の複合繊維に
よれば、溶融紡糸温度で液相となる耐熱性化合物が第1
成分と第2成分の間の界面の少なくとも一部に存在し、
繊維断面方向から見て前記複数成分のうち少なくとも1
成分が2個以上に分割されており、各成分は各々が繊維
断面の構成単位となっており、各構成単位は互に異なる
成分の構成単位と隣接し、かつ実質的に大部分の各構成
単位はその一部を繊維表面に露出しているので、圧力水
などの圧力流体の物理的衝撃処理によって分割が容易な
複合繊維及びその集合物とすることができる。また複合
繊維の構成成分であるポリマの種類を問わずに分割でき
る。Effects of the Invention As explained above, according to the composite fiber of the present invention, the heat-resistant compound that becomes a liquid phase at the melt spinning temperature is the first
present at least in part at the interface between the component and the second component;
At least one of the plurality of components as viewed from the fiber cross-sectional direction
The component is divided into two or more parts, each component is a constituent unit of the fiber cross section, each constituent unit is adjacent to a constituent unit of a different component, and substantially the majority of each constituent Since a portion of the unit is exposed on the fiber surface, the composite fiber and its aggregate can be easily split by physical impact treatment with a pressure fluid such as pressurized water. Furthermore, it can be divided regardless of the type of polymer that is a component of the composite fiber.
【0040】また、溶融紡糸温度で液相となる耐熱性化
合物がオルガノポリシロキサンおよびこれらの変性体で
あるという本発明の好ましい構成によれば、さらに分割
が容易となる。Further, according to a preferred configuration of the present invention in which the heat-resistant compound that becomes a liquid phase at the melt spinning temperature is an organopolysiloxane or a modified product thereof, division becomes even easier.
【0041】また、本発明の繊維集合物によれば、極細
の分割繊維を含み、絡合一体性にも優れているので、濾
過布、抄紙用カンバスなどの濾過用産業資材などに有用
なものとすることができる。Furthermore, the fiber aggregate of the present invention contains ultra-fine split fibers and has excellent entanglement integrity, so it is useful for industrial materials for filtration such as filter cloth and papermaking canvas. It can be done.
【図1】本発明の一実施例の複合繊維の繊維断面図であ
る。FIG. 1 is a cross-sectional view of a composite fiber according to an embodiment of the present invention.
【図2】本発明の一実施例の複合紡糸の概念モデル図で
ある。FIG. 2 is a conceptual model diagram of composite spinning according to an embodiment of the present invention.
【図3】本発明の一実施例の複合紡糸の概念モデル図で
ある。FIG. 3 is a conceptual model diagram of composite spinning according to an embodiment of the present invention.
【図4】本発明の一実施例の複合紡糸の概念モデル図で
ある。FIG. 4 is a conceptual model diagram of composite spinning according to an embodiment of the present invention.
1 A成分
2 B成分
11 シリコンオイル分散ポリマの流路12 通常
のポリマの流路
13 シリコンオイル分散ポリマ又はシリコンオイル
若しくはその変性体の流路1 Component A 2 Component B 11 Flow path of silicone oil-dispersed polymer 12 Flow path of ordinary polymer 13 Flow path of silicone oil-dispersed polymer, silicone oil, or modified product thereof
Claims (3)
0の範囲の熱可塑性樹脂からなる第1成分と第2成分で
少なくとも構成された複合繊維において、溶融紡糸温度
で液相となる耐熱性化合物が第1成分と第2成分の間の
界面の少なくとも一部に存在し、繊維断面方向から見て
前記複数成分のうち少なくとも1成分が2個以上に分割
されており、各成分は各々が繊維断面の構成単位となっ
ており、各構成単位は互に異なる成分の構成単位と隣接
し、かつ実質的に大部分の各構成単位はその一部を繊維
表面に露出していることを特徴とする分割性複合繊維。Claim 1: Melting point (Tm°C) is 100<Tm<35
In a composite fiber composed of at least a first component and a second component made of a thermoplastic resin in the range of At least one of the plurality of components is divided into two or more components when viewed from the cross-sectional direction of the fiber, and each component is a constituent unit of the fiber cross-section, and each constituent unit is mutually divided. 1. A splittable conjugate fiber characterized in that it is adjacent to constitutional units of different components, and that substantially most of each constitutional unit has a part exposed on the fiber surface.
物がオルガノポリシロキサンおよびこれらの変性体であ
る請求項1記載の分割性複合繊維。2. The splittable conjugate fiber according to claim 1, wherein the heat-resistant compound that becomes a liquid phase at the melt spinning temperature is an organopolysiloxane or a modified product thereof.
も30重量%含まれており、かつ前記複合繊維が分割さ
れてなる繊維集合物。3. A fiber aggregate containing at least 30% by weight of the splittable conjugate fiber according to claim 1, wherein the conjugate fiber is split.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5281491A JP3074028B2 (en) | 1991-03-18 | 1991-03-18 | Splittable conjugate fiber and its fiber aggregate for pressure fluid impact treatment |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5281491A JP3074028B2 (en) | 1991-03-18 | 1991-03-18 | Splittable conjugate fiber and its fiber aggregate for pressure fluid impact treatment |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04289222A true JPH04289222A (en) | 1992-10-14 |
JP3074028B2 JP3074028B2 (en) | 2000-08-07 |
Family
ID=12925317
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5281491A Expired - Lifetime JP3074028B2 (en) | 1991-03-18 | 1991-03-18 | Splittable conjugate fiber and its fiber aggregate for pressure fluid impact treatment |
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---|---|
JP (1) | JP3074028B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000053831A1 (en) * | 1999-03-08 | 2000-09-14 | Chisso Corporation | Split type conjugate fiber, method for producing the same and fiber formed article using the same |
JP2000303337A (en) * | 1999-03-01 | 2000-10-31 | Carl Freudenberg:Fa | Non-woven fabric made from thermally binding filament or fiber |
US6200669B1 (en) | 1996-11-26 | 2001-03-13 | Kimberly-Clark Worldwide, Inc. | Entangled nonwoven fabrics and methods for forming the same |
US6495255B2 (en) | 2000-06-26 | 2002-12-17 | Chisso Corporation | Polyolefin splittable conjugate fiber and a fiber structure using the same |
-
1991
- 1991-03-18 JP JP5281491A patent/JP3074028B2/en not_active Expired - Lifetime
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6200669B1 (en) | 1996-11-26 | 2001-03-13 | Kimberly-Clark Worldwide, Inc. | Entangled nonwoven fabrics and methods for forming the same |
JP2000303337A (en) * | 1999-03-01 | 2000-10-31 | Carl Freudenberg:Fa | Non-woven fabric made from thermally binding filament or fiber |
WO2000053831A1 (en) * | 1999-03-08 | 2000-09-14 | Chisso Corporation | Split type conjugate fiber, method for producing the same and fiber formed article using the same |
US6410139B1 (en) | 1999-03-08 | 2002-06-25 | Chisso Corporation | Split type conjugate fiber, method for producing the same and fiber formed article using the same |
US6617023B2 (en) | 1999-03-08 | 2003-09-09 | Chisso Corporation | Splittable multi-component fiber, method for producing it, and fibrous article comprising it |
DE10080786B3 (en) * | 1999-03-08 | 2015-05-13 | Jnc Corporation | Cleavable multicomponent fiber and fibrous article comprising it |
US6495255B2 (en) | 2000-06-26 | 2002-12-17 | Chisso Corporation | Polyolefin splittable conjugate fiber and a fiber structure using the same |
DE10130481B4 (en) * | 2000-06-26 | 2005-11-10 | Chisso Corp. | Cleavable conjugated polyolefin fiber and fiber structure using the same |
Also Published As
Publication number | Publication date |
---|---|
JP3074028B2 (en) | 2000-08-07 |
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