JP5045353B2 - Polyamide short fiber - Google Patents
Polyamide short fiber Download PDFInfo
- Publication number
- JP5045353B2 JP5045353B2 JP2007258392A JP2007258392A JP5045353B2 JP 5045353 B2 JP5045353 B2 JP 5045353B2 JP 2007258392 A JP2007258392 A JP 2007258392A JP 2007258392 A JP2007258392 A JP 2007258392A JP 5045353 B2 JP5045353 B2 JP 5045353B2
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- oil
- nonwoven fabric
- polyamide
- oil component
- 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
- 239000000835 fiber Substances 0.000 title claims description 93
- 239000004952 Polyamide Substances 0.000 title claims description 29
- 229920002647 polyamide Polymers 0.000 title claims description 29
- 239000004745 nonwoven fabric Substances 0.000 claims description 36
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 16
- 125000000129 anionic group Chemical group 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 239000003921 oil Substances 0.000 description 61
- 238000000034 method Methods 0.000 description 26
- 239000003795 chemical substances by application Substances 0.000 description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 238000004519 manufacturing process Methods 0.000 description 14
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 238000007380 fibre production Methods 0.000 description 7
- 238000005520 cutting process Methods 0.000 description 6
- 238000004804 winding Methods 0.000 description 6
- -1 bisamide compound Chemical class 0.000 description 5
- 229920000570 polyether Polymers 0.000 description 5
- 229920002302 Nylon 6,6 Polymers 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229920002292 Nylon 6 Polymers 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000000280 densification Methods 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 238000007696 Kjeldahl method Methods 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 229920005603 alternating copolymer Polymers 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000469 ethanolic extract Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- DJZKNOVUNYPPEE-UHFFFAOYSA-N tetradecane-1,4,11,14-tetracarboxamide Chemical compound NC(=O)CCCC(C(N)=O)CCCCCCC(C(N)=O)CCCC(N)=O DJZKNOVUNYPPEE-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Description
本発明は、繊維製造工程の通過性に優れ、かつ特に湿式不織布加工性に優れたポリアミド短繊維に関する。 The present invention relates to a short polyamide fiber having excellent permeability in a fiber production process and particularly excellent in wet nonwoven fabric processability.
ポリアミド繊維は従来から汎用合成繊維として広く知られており、短繊維としては、紡績糸からなる衣料や、様々な不織布からなる資材用途など様々な分野に用いられている。 Conventionally, polyamide fibers have been widely known as general-purpose synthetic fibers, and short fibers are used in various fields such as apparel made of spun yarn and material use made of various non-woven fabrics.
ポリアミド短繊維は、汎用合成繊維の中において比較的優れた強伸度特性、ソフトな触感、独特の風合い、適度な吸湿性などの特徴を有しており、不織布として用いた場合に、耐摩耗性などの物理的な耐久性や、耐薬品性などの化学的な耐久性に優れた構造体を得ることができる。 Polyamide short fiber has characteristics such as comparatively excellent strength and elongation characteristics, soft touch, unique texture, moderate hygroscopicity among general-purpose synthetic fibers, and wear resistance when used as a non-woven fabric. It is possible to obtain a structure excellent in physical durability such as property and chemical durability such as chemical resistance.
このような不織布は、具体的には、電池セパレーター用途、抄紙フェルト用途や研磨剤用途などに使用されている。 Specifically, such nonwoven fabrics are used for battery separators, papermaking felts, abrasives, and the like.
従来、短繊維はサーマルボンドなどのいわゆる乾式製法にて不織布に加工される例が多かったが、不織布の緻密化などの高性能化が要求される中で、高い緻密性が得られやすい湿式不織布の需要が拡大してきている。 Conventionally, short fibers were often processed into non-woven fabrics by so-called dry manufacturing methods such as thermal bonding, but wet non-woven fabrics that are easy to obtain high densification while high performance such as densification of non-woven fabrics is required. Demand is growing.
湿式不織布と乾式不織布では加工方法が大きく異なるので、原綿のスペックもそれに対応したものでなくてはならない。湿式不織布は、短繊維を水に分散させ、抄造することにより得られる。このように湿式不織布の製造においては水浴中にて短繊維を分散させる工程があり、ここでの短繊維の分散性が良好であることが求められる。 Since wet nonwoven fabrics and dry nonwoven fabrics have different processing methods, the specifications of the raw cotton must also correspond to them. The wet nonwoven fabric is obtained by dispersing short fibers in water and making paper. Thus, in the manufacture of a wet nonwoven fabric, there is a step of dispersing short fibers in a water bath, and the dispersibility of the short fibers here is required to be good.
ポリアミドは元々親水性を有する素材であるが、通常そのままでは水浴中での分散性は不十分であり、繊維の親水性を高めるような油剤(以下、親水性油剤という)を付与した後に使用される。 Polyamide is originally a hydrophilic material, but if used as it is, its dispersibility in a water bath is usually insufficient, and it is used after applying an oil agent (hereinafter referred to as a hydrophilic oil agent) that increases the hydrophilicity of the fiber. The
しかし、親水性油剤は、粘着性を有しており、繊維製造工程での通過性は悪い傾向が強い。 However, the hydrophilic oil agent has adhesiveness and tends to have poor permeability in the fiber production process.
繊維製造工程での糸切れが多く、ローラーやガイド類への巻付トラブルが発生すると、その糸切れの端糸部分がトウに含まれていると、張力がかからないまま短繊維へと切断されるため、所望の繊維長よりも長い繊維長、すなわち異常長を有する繊維の発生につながることがある。 When there are many yarn breaks in the fiber manufacturing process and winding trouble occurs on rollers and guides, if the end yarn part of the yarn break is included in the tow, it is cut into short fibers without applying tension. Therefore, a fiber length longer than the desired fiber length, that is, a fiber having an abnormal length may be generated.
そのため、繊維製造工程では、繊維の親水性を高める効果には劣るが、工程通過性に優れる鉱物油などのオイル類を含む油剤を付与し、その後の繊維切断工程などで親水性油剤の浴などを通して、親水性油剤を付与し直すという方法も使用されている。ここでいう親水性油剤は分散剤とも呼ばれる。 Therefore, in the fiber manufacturing process, the effect of increasing the hydrophilicity of the fiber is inferior, but an oil containing an oil such as mineral oil having excellent process passability is applied, and a hydrophilic oil bath is used in the subsequent fiber cutting process. A method of re-applying a hydrophilic oil agent is also used. The hydrophilic oil agent here is also called a dispersant.
この方法は、油剤付与が二度手間であり生産効率が悪い上、先に付与した工程通過油剤を事実上脱油することになり、排水負荷が大きくなるという不都合がある。 This method has the inconvenience that adding the oil agent is troublesome twice, the production efficiency is poor, and the process-passing oil agent previously applied is practically deoiled, resulting in a large drainage load.
そこで、繊維製造工程から高次加工まで一貫して工程通過性に優れるとともに繊維の親水性を高めることができる油剤成分が求められている。 Therefore, there is a demand for an oil component that is consistently excellent in process passability from the fiber production process to the higher-order processing and can increase the hydrophilicity of the fiber.
ポリアミド短繊維を湿式不織布になす例はこれまでに知られており、特許文献1〜3には湿式不織布に使用するためのポリアミド短繊維の製造方法が開示されているが、特許文献1では特定の水分率を有する長繊維束を回転刃式繊維束切断装置により切断することが開示され、特許文献2ではビスアミド化合物を含有させたポリアミド成分を繊維表面に露出させることが開示され、特許文献3では繊維の断面形状を多葉形状とすることが開示されているだけで、使用する油剤については具体的に示されておらず、上記要求を満たすような油剤成分はこれまでに見出されていなかった。
本発明は、かかる従来技術の背景に鑑み、繊維製造工程の通過性に優れ、湿式不織布への使用に適したポリアミド短繊維を提供することを目的とする。 The present invention has been made in view of the background of the prior art, and an object of the present invention is to provide a short polyamide fiber that is excellent in passability in a fiber production process and suitable for use in a wet nonwoven fabric.
本発明は、かかる課題を解決するために、次のような手段を採用するものである。
すなわち、炭素数が10〜14である直鎖状炭化水素基を有するアニオン系油剤成分と、炭素数が10〜14である直鎖状炭化水素基を有するノニオン系油剤成分とが付着してなり、前記油剤成分の総付着量が繊維重量当り0.2〜0.8重量%であり、かつ、繊維長が2〜10mmの範囲であることを特徴とする湿式不織布用ポリアミド短繊維である。
The present invention employs the following means in order to solve such problems.
That is, the anionic oil component having a linear hydrocarbon group having a carbon number is 10 to 14, becomes attached and a nonionic oil component having a linear hydrocarbon group having a carbon number is 10 to 14 , the total adhesion amount of the oil component is 0.2 to 0.8 wt% per fiber weight, and is wet-laid nonwoven fabric for polyamide short fibers fiber length and wherein the range der Rukoto of 2~10mm .
本発明によれば、製糸工程通過性が良好で、かつ湿式不織布加工性も優れたポリアミド短繊維を得ることができる。 According to the present invention, it is possible to obtain a polyamide short fiber having good yarn-making process passing properties and excellent wet nonwoven fabric processability.
本発明者らは、製糸工程通過性と湿式不織布加工性の両方をともに満たすポリアミド短繊維に関し、鋭意検討したところ、特定の油剤成分を付与することで、かかる課題を一挙に解決することを究明したものである。 The inventors of the present invention have made extensive studies on polyamide short fibers that satisfy both the yarn processability and the wet nonwoven fabric processability, and have found that this problem can be solved at once by adding a specific oil component. It is a thing.
本発明のポリアミド短繊維に使用するポリアミドは、繊維に形成できるポリアミドであれば、好ましく用いることができる。中でも、汎用性に優れるポリカプラミドやポリヘキサメチレンアジパミドを好ましく使用できるが、中でも耐熱性が高く、各種資材用途に好適に用いることができるヘキサメチレンアジパミドを特に好ましく使用することができる。また、他にもナイロン12や、本発明の効果を損ねない範囲において共重合成分を有するポリアミドを好適に用いることができる。 If the polyamide used for the polyamide short fiber of this invention is a polyamide which can be formed in a fiber, it can be preferably used. Among them, polycapramide and polyhexamethylene adipamide having excellent versatility can be preferably used, but hexamethylene adipamide which has high heat resistance and can be suitably used for various materials can be particularly preferably used. In addition, nylon 12 and polyamide having a copolymer component can be suitably used within a range not impairing the effects of the present invention.
本発明のポリアミド短繊維は単成分繊維に限るものではなく、芯鞘構造や海島構造などの複合繊維でも構わない。例えば熱接着バインダーとして使用できるポリヘキサメチレンアジパミドとポリカプラミドなどの組み合わせによる20℃以上の融点差を有する芯鞘複合繊維も好ましい。
本発明のポリアミド短繊維は、炭素数が10〜14である直鎖状炭化水素基を有するアニオン系油剤成分と、炭素数が10〜14である直鎖状炭化水素基を有するノニオン系油剤成分とが付着してなることが必要である。かかる油剤成分が付着した繊維は、繊維製造における工程通過性に優れるとともに、湿式不織布加工時における水浴中での分散を行うために必要とされる性能である親水性にも優れたものとなる。
The polyamide short fiber of the present invention is not limited to a single component fiber, and may be a composite fiber having a core-sheath structure or a sea-island structure. For example, a core-sheath composite fiber having a melting point difference of 20 ° C. or higher due to a combination of polyhexamethylene adipamide and polycapramide that can be used as a heat bonding binder is also preferable.
The polyamide short fiber of the present invention comprises an anionic oil component having a linear hydrocarbon group having 10 to 14 carbon atoms and a nonionic oil component having a linear hydrocarbon group having 10 to 14 carbon atoms. It is necessary to be attached. The fiber to which the oil component is attached has excellent processability in fiber production, and also has excellent hydrophilicity, which is a performance required for dispersion in a water bath during wet nonwoven fabric processing.
炭素数が10〜14である直鎖状炭化水素基を有するノニオン系油剤成分としては、例えば炭素数が10〜14の直鎖状炭化水素基を有するポリエーテル類や脂肪酸エステル類を用いることができる。直鎖状炭化水素基としては、直鎖状アルキル、直鎖状アルケニルなどが例示できる。また、かかるノニオン系油剤成分には、エチレンオキサイド、プロピレンオキサイド、ブチレンオキサイドなどが付加されていたり、複数のモノマー成分の組み合わせからなるブロック共重合体、ランダム共重合体、交互共重合体などが含まれていても構わないし、ノニオン系油剤成分の分子鎖中には分枝構造を有するアルキル基、ヒドロキシル基、アミド基、アミノ基などの官能機を含んでいても構わない。 As a nonionic oil agent component having a linear hydrocarbon group having 10 to 14 carbon atoms, for example, polyethers or fatty acid esters having a linear hydrocarbon group having 10 to 14 carbon atoms may be used. it can. Examples of the linear hydrocarbon group include linear alkyl and linear alkenyl. In addition, such nonionic oil components include ethylene oxide, propylene oxide, butylene oxide, etc., and block copolymers, random copolymers, alternating copolymers, etc. composed of combinations of a plurality of monomer components. The molecular chain of the nonionic oil component may contain a functional group such as an alkyl group having a branched structure, a hydroxyl group, an amide group, or an amino group.
炭素数が10〜14の直鎖状炭化水素基を有するポリエーテル類の場合、その重量平均分子量は、200〜20000の範囲内であることが好ましく、400〜15000の範囲内であることがより好ましい。かかる重量平均分子量が小さすぎると、粘着性が高くなりすぎて、繊維製造工程にて油剤成分が脱落しやすい傾向を示し、工程内のローラーでの巻き付きトラブルが多発することがあり、かかる重量平均分子量が大きすぎると、湿式不織布加工時の水中分散性が悪くなることがある。 In the case of a polyether having a linear hydrocarbon group having 10 to 14 carbon atoms, its weight average molecular weight is preferably in the range of 200 to 20000, more preferably in the range of 400 to 15000. preferable. If the weight average molecular weight is too small, the tackiness becomes too high, and the oil component tends to drop off in the fiber production process, and the trouble of winding with the roller in the process may occur frequently. If the molecular weight is too large, the dispersibility in water at the time of wet nonwoven fabric processing may deteriorate.
炭素数が10〜14である直鎖状炭化水素基を有するアニオン系油剤成分としては、例えば炭素数が10〜14の直鎖状炭化水素基を有するアルキルホスフェート類やサルフェート類などのアルカリ金属塩が使用できる。 Examples of the anionic oil agent component having a linear hydrocarbon group having 10 to 14 carbon atoms include alkali metal salts such as alkyl phosphates and sulfates having a linear hydrocarbon group having 10 to 14 carbon atoms. Can be used.
かかるアルカリ金属塩におけるアルカリ金属は、ナトリウムやカリウムを好ましく選択できる。 As the alkali metal in the alkali metal salt, sodium or potassium can be preferably selected.
本発明で使用する油剤成分においては、炭素数が10〜14の直鎖状炭化水素基を有することが必要であるが、これは、製糸工程における工程通過性と繊維への親水性付与という、一般に相反する二つの性質を満たすためである。炭素数が10未満の炭化水素基を有する油剤を使用した場合は、繊維への親水性付与効果に優れ、湿式不織布製造工程における短繊維の水中分散性は良好であるが、油剤の粘着性が高いことにより、繊維製造工程において、ローラーやガイド類への巻き付きが増加することになる。また、逆に炭素数が15以上の直鎖状炭化水素構造を有する油剤を使用する場合には、得られる繊維の平滑性に優れ、繊維と金属との摩擦係数も低下するので、繊維製造工程における通過性は良好となるが、湿式不織布製造工程における短繊維の水中分散性が不十分となり、分散性を得るためには、新たに親水性の油剤成分を追油する必要性が生じる。 In the oil agent component used in the present invention, it is necessary to have a linear hydrocarbon group having 10 to 14 carbon atoms. This is called process passability in the yarn making process and imparting hydrophilicity to the fiber. This is because it generally satisfies two contradictory properties. When an oil agent having a hydrocarbon group with a carbon number of less than 10 is used, it is excellent in the effect of imparting hydrophilicity to the fiber, and the dispersibility of short fibers in the wet nonwoven fabric manufacturing process is good, but the adhesive property of the oil agent is By being high, in the fiber manufacturing process, winding around the rollers and guides increases. On the contrary, when an oil agent having a linear hydrocarbon structure having 15 or more carbon atoms is used, the resulting fiber has excellent smoothness, and the friction coefficient between the fiber and the metal also decreases. However, the dispersibility of short fibers in water in the wet nonwoven fabric manufacturing process becomes insufficient, and in order to obtain dispersibility, it becomes necessary to newly add a hydrophilic oil component.
アニオン系油剤成分とノニオン系油剤成分がいずれも、炭素数が10〜14の直鎖状炭化水素基を有するという条件を満たしているため、アニオン系油剤成分とノニオン系油剤成分を混合し使用することができ、その製造方法に合わせた最適な混合比率を選択することができる。 Since both the anionic oil component and the nonionic oil component satisfy the condition of having a linear hydrocarbon group having 10 to 14 carbon atoms, the anionic oil component and the nonionic oil component are mixed and used. It is possible to select an optimum mixing ratio in accordance with the manufacturing method.
たとえば、アニオン系油剤成分とノニオン系油剤成分の重量比率は10/90〜60/40の範囲であることが好ましい。アニオン系油剤成分の含まれる重量比率が10%未満であると冬場などの湿度の低い季節などに繊維製造工程にて静電気が発生したり、湿式不織布加工時の水中分散性が悪くなることが観られることがある。また、アニオン系油剤成分の含まれる重量比率が60%を超えると、水中分散時に泡立ちが多くなることがあるので、撹拌速度を下げたり、消泡剤を添加する必要が生じることがある。 For example, the weight ratio of the anionic oil component to the nonionic oil component is preferably in the range of 10/90 to 60/40. If the weight ratio of the anionic oil component is less than 10%, static electricity is generated in the fiber manufacturing process in low humidity seasons such as winter, and the dispersibility in water during wet nonwoven fabric processing deteriorates. May be. Further, if the weight ratio of the anionic oil component exceeds 60%, foaming may increase during dispersion in water, so that it may be necessary to reduce the stirring speed or to add an antifoaming agent.
また、繊維に対する前記油剤成分の総付着量、すなわち油分量は、それが低すぎると湿式不織布加工時に水浴中での分散不良が生じることや、工程での擦過や静電気の発生により繊維製造工程における通過性が悪化するため好ましくなく、また油分が高すぎると製糸工程での油剤脱落が多くなり、そのためローラー類への巻き付きが発生しやすくなり、操業性が悪化するため好ましくない。好ましい範囲は繊維重量に対して、0.2〜0.8重量%の範囲内であり、より好ましくは0.4〜0.6重量%の範囲内である。 Moreover, the total adhesion amount of the oil component to the fiber, that is, the oil amount is too low in the fiber manufacturing process due to poor dispersion in the water bath during wet nonwoven fabric processing, and generation of abrasion and static electricity in the process. It is not preferable because the passability deteriorates, and if the oil content is too high, the oil agent will drop off in the yarn forming process, so that winding around the rollers tends to occur and the operability deteriorates, which is not preferable. A preferred range is in the range of 0.2 to 0.8% by weight, more preferably in the range of 0.4 to 0.6% by weight, based on the fiber weight.
ポリアミド短繊維の親水性を損ねるような成分はできるだけ付着させないようにすることが肝要である。例えばシリコーン系の成分や中性オイル成分などは、通常のポリアミド短繊維の油剤成分として一般的に使用されることがあるが、本発明においては極力付着させないようにする。 It is important that components that impair the hydrophilicity of the polyamide short fibers are not attached as much as possible. For example, a silicone-based component, a neutral oil component, and the like are generally used as an oil agent component of a normal polyamide short fiber, but in the present invention, they are not adhered as much as possible.
本発明のポリアミド短繊維の繊維長は、2〜10mmの範囲であることが好ましい。かかる繊維長が小さすぎる場合には、かかる短繊維を得るための長繊維を切断する工程で繊維の融着が発生しやすく、湿式不織布に加工する際に水浴中の分散不良繊維が多発することになる。また、かかる繊維長が大きすぎる場合には、繊維間の絡合が強くなり、湿式不織布に加工する際に水浴中での分散性が悪くなる。 The fiber length of the polyamide short fiber of the present invention is preferably in the range of 2 to 10 mm. If the fiber length is too small, fiber fusion tends to occur in the process of cutting the long fiber to obtain such short fibers, and poorly dispersed fibers in the water bath frequently occur when processing into a wet nonwoven fabric. become. Moreover, when this fiber length is too large, the entanglement between fibers will become strong and the dispersibility in a water bath will worsen when processing into a wet nonwoven fabric.
本発明のポリアミド短繊維は、ポリアミドのトウ形状の繊維に、前述した油剤成分を水に分散させた分散液、いわゆる油剤を付与し、乾燥して、所望の、具体的には前述した繊維長となるように切断することにより製造することができる。油剤は、繊維製造工程での通過性を考慮し、トウ状の繊維に延伸を実施する前に付与するのが良いが、油剤の付与方法としては、一本一本の繊維表面に対する均一付与や、前述した付着量の制御しやすさを考慮すると、油剤浴中にトウ形状の繊維を通過させ、含浸させ後にニップローラーで余剰分を絞り落とす方法を採用するのが好ましい。 The polyamide short fiber of the present invention is obtained by applying a dispersion obtained by dispersing the above-described oil component in water, a so-called oil agent, to a polyamide tow-shaped fiber, and drying it to obtain a desired, specifically the above-described fiber length. It can manufacture by cut | disconnecting so that it may become. The oil agent should be applied to the tow-shaped fiber before stretching in consideration of the passability in the fiber production process. However, as an oil agent application method, uniform application to the surface of each individual fiber or In consideration of the ease of controlling the amount of adhesion described above, it is preferable to employ a method in which a tow-shaped fiber is passed through an oil bath, impregnated, and then the excess is squeezed out by a nip roller.
かくして得られるポリアミド短繊維の物理特性は、製糸工程及び湿式不織布通過性を悪化させない範囲であれば、特に限定されるものではないが、例えば、単繊維繊度は、湿式不織布として使用される際に、薄手化や緻密さなどの機能を活かすためには2dtex以下であることが好ましく、乾強度は、製糸工程や不織布加工工程での通過時の耐久性や、製品として実際に使用される際の耐久性を考えると、2cN/dtex以上であることが好ましい。ただし、乾強度が7cN/dtexを超えると繊維を切断する際にナイフに与える負担が著しく悪化し、繊維切断工程での操業性や製品収率が悪くなることがある。 The physical properties of the polyamide short fibers thus obtained are not particularly limited as long as they do not deteriorate the yarn making process and the wet nonwoven fabric permeability, but, for example, the single fiber fineness is used when used as a wet nonwoven fabric. In order to make use of functions such as thinning and denseness, it is preferably 2 dtex or less, and the dry strength is the durability when passing in the yarn making process and the nonwoven fabric processing process, and when actually used as a product In view of durability, it is preferably 2 cN / dtex or more. However, if the dry strength exceeds 7 cN / dtex, the burden on the knife when cutting the fiber is significantly deteriorated, and the operability and product yield in the fiber cutting process may be deteriorated.
本発明のポリアミド短繊維の乾伸度は、製糸工程や、不織布加工工程での通過性を考えると、30%以上であることが好ましく、最終製品である不織布の形態保持性を考えると、100%以下であることが好ましい。 The dry elongation of the polyamide short fiber of the present invention is preferably 30% or more in view of the passability in the yarn production process and the nonwoven fabric processing process, and 100 in view of the shape retention of the final product nonwoven fabric. % Or less is preferable.
なお、ここでいう繊度、乾強度、乾伸度は、JIS L 1015(1999年)(化学繊維ステープル試験法)に基づいて求められるものである。 The fineness, dry strength, and dry elongation referred to here are determined based on JIS L 1015 (1999) (chemical fiber staple test method).
本発明のポリアミド短繊維には捲縮が付与されていないことが好ましい。このようなストレート繊維であることが好ましい。捲縮が付与されていると、繊維間の絡合により、不織布加工時の水浴中の分散性が悪化するため好ましくない。 The polyamide short fibers of the present invention are preferably not crimped. Such straight fibers are preferred. If crimps are imparted, dispersibility in the water bath during processing of the nonwoven fabric deteriorates due to entanglement between the fibers, which is not preferable.
本発明のポリアミド短繊維を用いて得た湿式不織布は、エアフィルターなどのフィルター類に用いることができるばかりか、電池セパレーターとしての使用など、種々の用途に好ましく用いることができる。 The wet nonwoven fabric obtained by using the polyamide short fiber of the present invention can be used not only for filters such as an air filter but also preferably for various uses such as use as a battery separator.
以下、本発明を実施例を挙げてさらに具体的に説明する。各種物性の測定方法は次の通りである。 Hereinafter, the present invention will be described more specifically with reference to examples. The measuring method of various physical properties is as follows.
単繊維繊度、乾強度、乾伸度は、JIS L 1015(1999年)(化学繊維ステープル試験法)に準じて測定した。 Single fiber fineness, dry strength, and dry elongation were measured according to JIS L 1015 (1999) (chemical fiber staple test method).
油分は、ソックスレー管を用いたエタノール抽出分から、ケルダール法にて定量したポリアミドモノマー及びオリゴマーの重量を差し引き、算出した。 The oil content was calculated by subtracting the weight of the polyamide monomer and oligomer determined by the Kjeldahl method from the ethanol extract using a Soxhlet tube.
(実施例1)
酸化チタンを0.30重量%含有するナイロン66チップを、単軸のエクストルーダーにより280℃の温度にて溶融し、孔数が600ホールの口金を用いて紡出し、チムニーにより冷却した糸条を1300m/分の速度で引き取り、缶に収納することで未延伸糸を得た。
Example 1
A nylon 66 chip containing 0.30% by weight of titanium oxide was melted at a temperature of 280 ° C. by a single-screw extruder, spun using a base having a hole number of 600 holes, and cooled by chimney. The undrawn yarn was obtained by taking it up at a speed of 1300 m / min and storing it in a can.
得られた未延伸糸を50本束ねたトウを、延伸工程内において、油剤Aの濃度が1.5重量%になるように調整した油剤浴中を通過させ、ニップローラーで過剰の油剤を絞った後に、水蒸気を付与し、3.0倍に延伸を行い、トウを得た。 The tow obtained by bundling 50 undrawn yarns is passed through an oil bath adjusted so that the concentration of oil A is 1.5% by weight in the drawing process, and excess oil is squeezed with a nip roller. After that, steam was applied and stretched 3.0 times to obtain a tow.
油剤Aの組成は、デシル(C12)ホスフェートナトリウム塩と、分子鎖中にC12構造を含むポリエーテルを50:50の重量比で配合したものである。 The composition of the oil agent A is a blend of decyl (C12) phosphate sodium salt and a polyether having a C12 structure in the molecular chain in a weight ratio of 50:50.
トウを10t生産する際に、延伸ローラーへの巻付きトラブルの発生回数は2回であり、工程通過性は良好であった。 When 10 tons of tow was produced, the number of occurrences of the trouble of winding around the stretching roller was 2, and the process passability was good.
得られたトウをECローターにより繊維長5mmに切断し、短繊維を得た。この短繊維を、水浴中に撹拌しながら投入したところ、良好な分散性を示し、湿式不織布加工性も良好であった。繊維一般物性等の測定結果を表1に示す。 The obtained tow was cut into a fiber length of 5 mm with an EC rotor to obtain short fibers. When the short fibers were put into a water bath with stirring, they showed good dispersibility and good wet nonwoven fabric processability. Table 1 shows the measurement results of the general physical properties of the fiber.
(実施例2)
酸化チタンを0.30%含有するナイロン66チップを芯側に、酸化チタンを0.30%含有するナイロン6チップを鞘側に用い、芯鞘複合繊維として紡出すること以外は実施例1と同様に短繊維を製造した。繊維一般物性等の測定結果を表1に示す。
(Example 2)
Example 1 except that a nylon 66 tip containing 0.30% titanium oxide is used on the core side and a nylon 6 tip containing 0.30% titanium oxide is used on the sheath side and spinning as a core-sheath composite fiber. Short fibers were produced in the same way. Table 1 shows the measurement results of the general physical properties of the fiber.
(比較例1)
油剤Aを油剤Bに変更した以外は、実施例1と同様にして短繊維を製造した。
(Comparative Example 1)
Short fibers were produced in the same manner as in Example 1 except that the oil A was changed to the oil B.
ここで、油剤Bとはオクチル(C8)ホスフェートカリウム塩と、分子鎖中にC8構造を含むポリエーテルを50:50の重量比で配合したものである。 Here, the oil agent B is a mixture of octyl (C8) phosphate potassium salt and a polyether containing a C8 structure in the molecular chain in a weight ratio of 50:50.
トウを10t生産する際に、油剤の粘着に起因する延伸ローラーへの巻き付きは、20回発生し、操業性は悪いものであった。 When producing 10 tons of tow, winding around the stretching roller due to adhesion of the oil agent occurred 20 times, and the operability was poor.
繊維切断後に湿式不織布加工を実施する際に、水浴中での分散性は良好であった。 Dispersibility in a water bath was good when wet nonwoven fabric processing was performed after fiber cutting.
(比較例2)
油剤Aを油剤Cに変更した以外は、実施例1と同様にして短繊維を製造した。
(Comparative Example 2)
Short fibers were produced in the same manner as in Example 1 except that the oil A was changed to the oil C.
ここで、油剤Cとはセチル(C16)ホスフェートカリウム塩と、分子鎖中にC16構造を含むポリエーテルを50:50の重量比で配合したものである。 Here, the oil agent C is a mixture of cetyl (C16) phosphate potassium salt and a polyether containing a C16 structure in the molecular chain in a weight ratio of 50:50.
得られた短繊維を、水浴中に撹拌しながら投入したところ、水浴中での分散時に均一性に欠けるため、得られた不織布にはシワが観られ、地合が悪いものであった。 When the obtained short fibers were put into a water bath with stirring, they were not uniform when dispersed in the water bath, and thus the resulting nonwoven fabric was wrinkled, and the texture was poor.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007258392A JP5045353B2 (en) | 2007-10-02 | 2007-10-02 | Polyamide short fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007258392A JP5045353B2 (en) | 2007-10-02 | 2007-10-02 | Polyamide short fiber |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2009084760A JP2009084760A (en) | 2009-04-23 |
JP2009084760A5 JP2009084760A5 (en) | 2010-11-18 |
JP5045353B2 true JP5045353B2 (en) | 2012-10-10 |
Family
ID=40658541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2007258392A Expired - Fee Related JP5045353B2 (en) | 2007-10-02 | 2007-10-02 | Polyamide short fiber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP5045353B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111225998B (en) * | 2017-10-20 | 2023-01-24 | 英威达纺织(英国)有限公司 | High-bearing-capacity nylon staple fiber with additive, blended yarn and fabric thereof |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004043995A (en) * | 2002-07-09 | 2004-02-12 | Sanyo Chem Ind Ltd | Synthetic fiber oiling agent for making paper |
-
2007
- 2007-10-02 JP JP2007258392A patent/JP5045353B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP2009084760A (en) | 2009-04-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO1994023098A1 (en) | Polytetrafluoroethylene fiber, cottony material containing the same, and process for producing the same | |
CN101671918B (en) | Process for producing full nylon leather base fabric | |
TWI686520B (en) | Polyester binder fiber | |
KR20170100480A (en) | Polyphenylene sulfide monofilament and manufacturing method therefor, and package | |
EP0311860B1 (en) | Nonwoven fabric made of heat bondable fibers | |
JP6206040B2 (en) | Polyphenylene sulfide fiber for nonwoven fabric | |
JP2005330643A (en) | Heat-resistant wet type nonwoven fabric | |
JP5045353B2 (en) | Polyamide short fiber | |
JP2008261081A (en) | Splittable conjugate fiber containing polyacetal, and molded fiber material and product each using the same | |
JPS63243324A (en) | Heat bonding fiber and nonwoven fabric thereof | |
JP5846901B2 (en) | Polyester composite binder fiber | |
JP2013122102A (en) | Wet nonwoven fabric | |
KR20210060458A (en) | Copolymerized polyphenylene sulfide fiber | |
JP2008223198A (en) | Method for producing polyamide fiber | |
JP4455180B2 (en) | Short fiber for nonwoven fabric and short fiber nonwoven fabric | |
JP6068868B2 (en) | Shortcut fiber for wet nonwoven fabric | |
JP7427882B2 (en) | Nonwoven fabric using eccentric core-sheath composite short fibers | |
JP4624094B2 (en) | Polyester no crimp fiber | |
JP2003171870A (en) | Polyketone fiber | |
JP2008007889A (en) | Polyester staple fiber | |
JP2007204870A (en) | Polyamide staple fiber and method for producing the same | |
JP4468025B2 (en) | Split composite fiber and polyamide fiber structure | |
JP4854166B2 (en) | High-speed false twisting method for polylactic acid multifilament yarn | |
JP3833622B2 (en) | Method for producing polyester conjugate fiber and polyester conjugate fiber obtained by the production method | |
JP2022117559A (en) | polyphenylene sulfide fiber |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20101001 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20101001 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20120125 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20120131 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20120619 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20120702 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20150727 Year of fee payment: 3 |
|
R151 | Written notification of patent or utility model registration |
Ref document number: 5045353 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R151 |
|
LAPS | Cancellation because of no payment of annual fees |