JP2011174198A - Aromatic polyamide staple fiber - Google Patents
Aromatic polyamide staple fiber Download PDFInfo
- Publication number
- JP2011174198A JP2011174198A JP2010038805A JP2010038805A JP2011174198A JP 2011174198 A JP2011174198 A JP 2011174198A JP 2010038805 A JP2010038805 A JP 2010038805A JP 2010038805 A JP2010038805 A JP 2010038805A JP 2011174198 A JP2011174198 A JP 2011174198A
- Authority
- JP
- Japan
- Prior art keywords
- aromatic polyamide
- fiber
- weight
- short fiber
- oil
- 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 76
- 239000004760 aramid Substances 0.000 title claims abstract description 53
- 229920003235 aromatic polyamide Polymers 0.000 title claims abstract description 52
- -1 alkali metal salt Chemical class 0.000 claims abstract description 25
- 239000000839 emulsion Substances 0.000 claims abstract description 13
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 10
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 8
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 33
- 238000009987 spinning Methods 0.000 claims description 19
- 229910019142 PO4 Inorganic materials 0.000 claims description 10
- 239000010452 phosphate Substances 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 32
- 238000000034 method Methods 0.000 description 17
- 230000005611 electricity Effects 0.000 description 8
- 230000003068 static effect Effects 0.000 description 8
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 4
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 229920006231 aramid fiber Polymers 0.000 description 3
- 150000004984 aromatic diamines Chemical class 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 159000000000 sodium salts Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- UJDCDJDPWCGFTO-UHFFFAOYSA-N phosphono hexanoate Chemical compound CCCCCC(=O)OP(O)(O)=O UJDCDJDPWCGFTO-UHFFFAOYSA-N 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 2
- 238000004804 winding Methods 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- XBTRYWRVOBZSGM-UHFFFAOYSA-N (4-methylphenyl)methanediamine Chemical compound CC1=CC=C(C(N)N)C=C1 XBTRYWRVOBZSGM-UHFFFAOYSA-N 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- 239000004953 Aliphatic polyamide Substances 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 239000005635 Caprylic acid (CAS 124-07-2) Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241000047703 Nonion Species 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- ZJLATTXAOOPYRU-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CO)(CO)CO ZJLATTXAOOPYRU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920003231 aliphatic polyamide Polymers 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 206010061592 cardiac fibrillation Diseases 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- YVIGPQSYEAOLAD-UHFFFAOYSA-L disodium;dodecyl phosphate Chemical compound [Na+].[Na+].CCCCCCCCCCCCOP([O-])([O-])=O YVIGPQSYEAOLAD-UHFFFAOYSA-L 0.000 description 1
- UWLPCYBIJSLGQO-UHFFFAOYSA-N dodecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCC(O)=O UWLPCYBIJSLGQO-UHFFFAOYSA-N 0.000 description 1
- TVACALAUIQMRDF-UHFFFAOYSA-N dodecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCOP(O)(O)=O TVACALAUIQMRDF-UHFFFAOYSA-N 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000007378 ring spinning Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
Abstract
Description
本発明は芳香族ポリアミド短繊維、特には紡績性能に優れた芳香族ポリアミド短繊維に関する。 The present invention relates to an aromatic polyamide short fiber, and more particularly to an aromatic polyamide short fiber excellent in spinning performance.
芳香族ポリアミド繊維は、ポリエステル繊維や脂肪族ポリアミド繊維等の汎用合成繊維に比べ物性に優れ、近年では各種産業用途や機能性衣料として広く利用されている。中でも高結晶性で耐熱性に優れ大量生産に適することから、一定長に切断された短繊維が、消防服等の特に難燃性が要求される産業用資材や衣料用途に広く使用されている。 Aromatic polyamide fibers are superior in physical properties compared to general-purpose synthetic fibers such as polyester fibers and aliphatic polyamide fibers, and have been widely used in recent years for various industrial uses and functional clothing. Above all, short fibers cut to a certain length are widely used for industrial materials such as fire-fighting clothes and industrial applications and clothing that are highly crystalline and have excellent heat resistance and are suitable for mass production. .
しかし、芳香族ポリアミド繊維は他の合成繊維に比べて極めて静電気を帯び易く、紡績のカード工程でのシリンダー部への捲付き、あるいはウェア斑が発生し易く、安定した品質の紡績糸が得られないとの問題があった。さらに、粗紡や精紡工程では各種ローラやガイドとの擦過によって繊維がフィブリル化し易く、油剤の粘性も加わって糸導に堆積し易く清掃の頻度が多くなり、作業負担が大きく、作業効率が低下するという問題があった。特に近年では高速で紡績を実施するリング紡績やMJSに使用する場合が増え、繊維のフィブリル化が更に発生しやすく、スカムの付着やローラ捲付きが多く発生するため、紡績工程の通過性が極めて悪化してきているという問題が顕在化してきた。 However, aromatic polyamide fibers are much more electrostatically charged than other synthetic fibers, and are prone to wrinkling of the cylinder part or wear spots in the spinning card process, and a stable quality spun yarn can be obtained. There was no problem. Furthermore, in the roving and fine spinning processes, the fibers are easily fibrillated by rubbing with various rollers and guides, and the viscosity of the oil agent is added, so that the fibers are easily deposited on the yarn guide. There was a problem to do. Particularly in recent years, the use of ring spinning and MJS, which perform spinning at a high speed, has increased, fibrils are more likely to be fibrillated, and scum adherence and roller wrinkles often occur. The problem of getting worse has become apparent.
これらの問題に対し、特許文献1では、フィブリル化を抑制するために特定炭素数の長鎖アルキル燐酸エステル塩を含む処理剤が提案されている。しかしこの処理剤は特に低湿度下の条件において静電気が発生しやすいという問題があった。そこで特許文献2には若干炭素数の少ないアルキル燐酸エステル塩と含窒素ノニオン型の制電剤を併用することにより、集束性と制電性を両立させた処理剤が開示されている。しかしいずれの方法を用いた場合にも、静電気の発生を抑制しながら、スカムの発生やローラへの巻付きを十分には抑えることができない、という問題があった。 With respect to these problems, Patent Document 1 proposes a treatment agent containing a long-chain alkyl phosphate ester salt having a specific carbon number in order to suppress fibrillation. However, this treatment agent has a problem that static electricity is likely to be generated particularly under conditions of low humidity. Thus, Patent Document 2 discloses a treatment agent that achieves both convergence and antistatic properties by using an alkyl phosphate ester salt having a slightly smaller number of carbon atoms and a nitrogen-containing nonionic antistatic agent in combination. However, when any of the methods is used, there is a problem that generation of scum and winding around a roller cannot be sufficiently suppressed while suppressing generation of static electricity.
本発明は、工程通過性に優れた芳香族ポリアミド短繊維を提供することにある。 An object of the present invention is to provide an aromatic polyamide short fiber excellent in process passability.
本発明の芳香族ポリアミド短繊維は、芳香族ポリアミド繊維の表面に油剤が付着している芳香族ポリアミド短繊維であって、該油剤が(A)成分を50〜95重量%、(B)成分を5〜20重量%含有し、かつ該油剤の高濃度エマルジョン粘度が50Pa・s以下であることを特徴とする。
(A)炭素数が6〜12の燐酸エステルのアルカリ金属塩
(B)30℃での動粘度が5〜50mm2/sである多価アルコールのアルキレンオキサイド付加物。
The aromatic polyamide short fiber of the present invention is an aromatic polyamide short fiber in which an oil agent is attached to the surface of the aromatic polyamide fiber, and the oil agent comprises 50 to 95% by weight of the component (A) and the component (B). 5 to 20% by weight, and the high-concentration emulsion viscosity of the oil is 50 Pa · s or less.
(A) Alkali metal salt of phosphate ester having 6 to 12 carbon atoms (B) Alkylene oxide adduct of polyhydric alcohol having a kinematic viscosity at 30 ° C. of 5 to 50 mm 2 / s.
さらには、繊維重量に対する付着量が0.2〜1.0重量%であることや、芳香族ポリアミド繊維がポリメタフェニレンイソフタルアミド繊維であることが好ましい。
そして、本発明の紡績糸は、上記本発明の芳香族ポリアミド短繊維からなるものであり、紡績することを特徴とする。
Furthermore, the adhesion amount with respect to the fiber weight is preferably 0.2 to 1.0% by weight, and the aromatic polyamide fiber is preferably a polymetaphenylene isophthalamide fiber.
The spun yarn of the present invention is made of the aromatic polyamide short fiber of the present invention and is spun.
本発明によれば、工程通過性に優れた芳香族ポリアミド短繊維が提供される。 ADVANTAGE OF THE INVENTION According to this invention, the aromatic polyamide short fiber excellent in process permeability is provided.
本発明は、芳香族ポリアミド繊維の表面に油剤が付着している芳香族ポリアミド短繊維に関するものである。ここで芳香族ポリアミド繊維を構成する芳香族ポリアミドについて述べると、一般式−NH−Ar1−NH−CO−Ar2−CO−及び/または−NH−Ar3−CO−なる繰返し単位(Ar1、Ar2、Ar3はそれぞれ独立に二価の芳香族基である)で表わされるものである。具体例としては、ポリパラフェニレンテレフタルアミド、ポリメタフェニレンイソフタルアミド、ポリパラベンゾアミド、ポリ-3,4′−オキシジフェニレンテレフタルアミド/ポリパラフェニレンテレフタルアミド共重合体である。 The present invention relates to an aromatic polyamide short fiber in which an oil agent is attached to the surface of an aromatic polyamide fiber. Here, the aromatic polyamide constituting the aromatic polyamide fiber will be described. The repeating unit represented by the general formula —NH—Ar 1 —NH—CO—Ar 2 —CO— and / or —NH—Ar 3 —CO— (Ar 1 , Ar 2 and Ar 3 are each independently a divalent aromatic group). Specific examples are polyparaphenylene terephthalamide, polymetaphenylene isophthalamide, polyparabenzamide, and poly-3,4'-oxydiphenylene terephthalamide / polyparaphenylene terephthalamide copolymer.
本発明の芳香族ポリアミド繊維は、以上のような芳香族ポリアミドからなるパラ系芳香族ポリアミド繊維(いわゆるパラ系アラミド繊維)やメタ系芳香族ポリアミド繊維(いわゆるメタ系アラミド繊維)を挙げることができるが、本発明の効果は短繊維として生産、加工が行われることが多いメタ系芳香族ポリアミド繊維であることが、特に好ましい。 Examples of the aromatic polyamide fiber of the present invention include para-aromatic polyamide fibers (so-called para-aramid fibers) and meta-aromatic polyamide fibers (so-called meta-aramid fibers) made of the aromatic polyamide as described above. However, the effect of the present invention is particularly preferably a meta-aromatic polyamide fiber that is often produced and processed as a short fiber.
ここでメタ系芳香族ポリアミドについてさらに詳細に述べると、下記(イ)〜(ハ)の芳香族ポリアミドを混合したポリマーからなる繊維であることが好ましい。
(イ)アミン成分が、キシレンジアミン35〜100モル%、芳香族ジアミン65〜0モル%、酸成分が芳香族ジカルボン酸からなるほう芳香族ポリアミド
(ロ)アミン成分が、炭素数1〜4のアルキル置換基を少なくとも1つ有するフェニレンジアミンまたは置換基を有さない芳香族ジアミンであり、酸成分が芳香族ジカルボン酸よりなる芳香族ポリアミド
(ハ)アミン成分が、1〜4のハロゲン置換基を有するフェニレンジアミン40〜100モル%と、置換基を有さない芳香族ジアミン60〜0モル%とからなり、酸成分が芳香族ジカルボン酸からなる芳香族ポリアミド。
When the meta-aromatic polyamide is described in more detail, it is preferably a fiber made of a polymer obtained by mixing the following aromatic polyamides (a) to (c).
(I) An amine component is 35-100 mol% xylenediamine, 65-0 mol% aromatic diamine, and an aromatic polyamide (ro) amine component consisting of an aromatic dicarboxylic acid has 1 to 4 carbon atoms. A phenylene diamine having at least one alkyl substituent or an aromatic diamine having no substituent, wherein the aromatic polyamide (c) amine component comprising an aromatic dicarboxylic acid has 1 to 4 halogen substituents An aromatic polyamide composed of 40 to 100 mol% of phenylenediamine and 60 to 0 mol% of an aromatic diamine having no substituent, wherein the acid component is an aromatic dicarboxylic acid.
そして好ましいメタ系芳香族ポリアミド繊維としては、20重量%までは、他の共重合成分を混合しても良く、共重合成分としては、パラ系芳香族ポリアミド成分であることが特に好ましい。 The preferred meta-aromatic polyamide fiber may be mixed with other copolymer components up to 20% by weight, and the copolymer component is particularly preferably a para-aromatic polyamide component.
なお、この好ましいメタ系芳香族ポリアミド繊維としては、固有粘度は、0.5g/100mlの濃硫酸溶液(30℃)で測定した値が0.8〜4.0、特に1.0〜3.0のものであることが好ましい。さらに、難燃剤、着色剤、耐光向上剤、艶消し剤、導電剤などの添加剤を、本発明の目的を損なわない範囲で含有してもよい。 In addition, as this preferable meta type | system | group aromatic polyamide fiber, the value measured by 0.5 g / 100 ml concentrated sulfuric acid solution (30 degreeC) is 0.8-4.0, especially 1.0-3. It is preferably zero. Furthermore, you may contain additives, such as a flame retardant, a coloring agent, a light fastness improving agent, a matting agent, and a electrically conductive agent, in the range which does not impair the objective of this invention.
また本発明の芳香族ポリアミド短繊維の長さとしては200mm以下、通常は0.2〜150mm、より好ましくは38〜76mmの範囲であることが好ましい。また繊度としては25dtex以下、通常は0.5〜15dtex、より好ましくは1.3〜3.3dtexの範囲であることが好ましい。このような形状の短繊維であると、紡績して紡績糸とすることが容易となる。 The length of the aromatic polyamide short fiber of the present invention is preferably 200 mm or less, usually 0.2 to 150 mm, more preferably 38 to 76 mm. The fineness is preferably 25 dtex or less, usually 0.5 to 15 dtex, more preferably 1.3 to 3.3 dtex. When the short fiber has such a shape, it becomes easy to spin and form a spun yarn.
本発明の芳香族ポリアミド繊維は、このような繊維の表面に油剤が付着しているものであって、その油剤が下記の(A)成分を50〜95重量%含有し、かつ(B)成分を5〜20重量%含有することを必須とするものである。
(A)炭素数が6〜12の燐酸エステルのアルカリ金属塩
(B)30℃での動粘度が5〜50mm2/sである多価アルコールのアルキレンオキサイド付加物。
The aromatic polyamide fiber of the present invention has an oil agent attached to the surface of such a fiber, and the oil agent contains 50 to 95% by weight of the following component (A), and component (B) It is essential to contain 5 to 20% by weight.
(A) Alkali metal salt of phosphate ester having 6 to 12 carbon atoms (B) Alkylene oxide adduct of polyhydric alcohol having a kinematic viscosity at 30 ° C. of 5 to 50 mm 2 / s.
ここで本発明において、芳香族ポリアミド系短繊維に付与せしめられる処理剤についてさらに説明をする。(A)成分である燐酸エステルのアルカリ金属塩は、空気中の水分を吸湿し易く、低湿度下の環境でも静電気の発生を抑制させることが可能となる。さらにこのようなアルカリ金属塩は、アラミド繊維表面に付着した油剤中に含有されることにより、紡績機のローラやガイド等と繊維との擦過によって、ガイド等の金属表面に吸着、配向し、繊維と金属との摩擦抵抗を低く保つことができる。そのため本発明の短繊維はカードや練条及び精紡工程での糸切れが防止され、生産性向上がはかられるのである。さらに、アラミド繊維の表面に存在するこのようなアルカリ金属塩は、吸湿した場合でも油剤の粘性を低く保たれている。本発明の短繊維は、紡績機でのローラ捲き付きが極めて少なくなり、紡績の工程通過性が極めて安定化するのである。 Here, the treatment agent imparted to the aromatic polyamide short fibers in the present invention will be further described. The alkali metal salt of phosphoric acid ester which is the component (A) can easily absorb moisture in the air, and can suppress the generation of static electricity even in a low humidity environment. Furthermore, such an alkali metal salt is contained in the oil agent adhering to the surface of the aramid fiber, so that the fiber is adsorbed and oriented on the metal surface of the guide or the like by rubbing the roller or guide of the spinning machine with the fiber. And the frictional resistance with the metal can be kept low. For this reason, the staple fiber of the present invention is prevented from being broken during carding, drawing, and spinning, thereby improving productivity. Further, such an alkali metal salt present on the surface of the aramid fiber keeps the viscosity of the oil agent low even when it absorbs moisture. In the short fiber of the present invention, roller sprinkling in the spinning machine is extremely reduced, and the spinning process passability is extremely stabilized.
このような本発明で使用される燐酸エステル塩は、従来より広く使用されている炭素数が6〜12の高級アルコールと無水燐酸から合成することが可能である。さらに本発明の効果をより発揮するためには、炭素数が6〜8の燐酸エステルのアルカリ金属塩であることが好ましい。本発明のアルカリ金属塩としては、ナトリウム塩、カリ塩、リチウム塩が好ましい。より具体的にはカプロイルホスフェートのカリ塩、カプロイルホスフェートのナトリウム塩、カプリルホスフェートのカリ塩、カプリルホスフェートのナトリウム塩、ラウリルホスフェートのカリ塩、ラウリルホスフェートのナトリウム塩等を挙げることができる。 Such phosphate ester salts used in the present invention can be synthesized from higher alcohols having 6 to 12 carbon atoms and phosphoric anhydride that have been widely used conventionally. Furthermore, in order to exhibit the effect of this invention more, it is preferable that it is a C6-C8 alkali metal salt of phosphate ester. As the alkali metal salt of the present invention, sodium salt, potassium salt and lithium salt are preferable. More specifically, examples include potassium salt of caproyl phosphate, sodium salt of caproyl phosphate, potassium salt of capryl phosphate, sodium salt of capryl phosphate, potassium salt of lauryl phosphate, sodium salt of lauryl phosphate, and the like.
本発明で用いる燐酸エステルのアルカリ金属塩の繊維表面に付着した油剤成分中の含有量としては、50〜95重量%であることが必要である。50重量%未満の場合、制電性が不良となり静電気発生に伴うローラ捲き付き等が発生し易く、紡績性を著しく損ない、使用が困難となる。逆に、95重量%を越えると油剤中の(B)成分が不足し、十分な効果を得ることができない。 As content in the oil agent component adhering to the fiber surface of the alkali metal salt of the phosphate ester used by this invention, it is required to be 50 to 95 weight%. If it is less than 50% by weight, the antistatic property is poor, and roller scoring due to the generation of static electricity is likely to occur, the spinnability is remarkably impaired, and the use becomes difficult. On the other hand, if it exceeds 95% by weight, the component (B) in the oil is insufficient, and a sufficient effect cannot be obtained.
次に(B)成分について説明する。(B)成分とは、30℃での動粘度が5〜50mm2/sである多価アルコールのアルキレンオキサイド付加物である。この(B)成分を本発明の短繊維に用いることによって、短繊維からなるスライバーに適度な集束性を付与することが可能となり、後工程のローラ捲付きの防止に特に有効である。 Next, the component (B) will be described. The component (B) is an alkylene oxide adduct of a polyhydric alcohol having a kinematic viscosity at 30 ° C. of 5 to 50 mm 2 / s. By using this component (B) for the short fibers of the present invention, it is possible to impart appropriate convergence to a sliver made of short fibers, which is particularly effective in preventing post-roller wrinkling.
通常、芳香族ポリアミド繊維を高速で紡績を実施する場合には、高速練条や超高速空気革新精紡機のMTS(ムラタ・ツインスピナー)、MJS(ムラタ・ジェットスピナー)等が200〜300m/分と高速なため、スライバーが金属やゴムローラー等の擦過によって集束性が低下するという問題があった。スライバーの一部の単糸が金属やゴムローラーに捲付き易くなり、紡績を続行することが困難になるためである。本発明の短繊維では、その現象を有効に抑えることが可能となったのである。 Usually, when spinning aromatic polyamide fibers at high speeds, high-speed kneading, MTS (Murata Twin Spinner), MJS (Murata Jet Spinner), etc. of ultra-high speed air innovative spinning machines are 200-300m / min. Because of the high speed, the sliver has a problem that the convergence is lowered by rubbing a metal or a rubber roller. This is because some of the single yarn of the sliver is likely to be caught on the metal or rubber roller, making it difficult to continue spinning. In the short fiber of the present invention, this phenomenon can be effectively suppressed.
このような本発明で使用される多価アルコールのエチレンオキサイド付加物は、例えばグリセリンやペンタエリスリトール、ソルビトール、あるいはソルビタンに脂肪酸及び水酸化ナトリウムを加え、加熱することによってエステル化反応させ、次いでエチレンオキサイドを付加させることで合成することが可能である。ここで多価アルコールと反応させる脂肪酸としては、炭素数8〜18の高級脂肪酸が好ましく、例えばカプリル酸、ラウリン酸、パルミチン酸、ステアリン酸等を挙げることができる。エチレンオキサイドの付加モル数として5〜40モルの範囲が好ましい。より具体的には、例えばグリセリンモノラウレートのエチレンオキサイド付加物、ペンタエリスリトールのエチレンオキサイド付加物、ソルビタンモノラウレートのエチレンオキサイド付加物、ソルビタンモノステアレートのエチレンオキサイド付加物、ペンタエリスリトールモノラウレート等を挙げることができる。 Such an ethylene oxide adduct of a polyhydric alcohol used in the present invention is, for example, an esterification reaction by adding a fatty acid and sodium hydroxide to glycerin, pentaerythritol, sorbitol, or sorbitan, followed by heating, and then ethylene oxide. Can be synthesized by adding. Here, the fatty acid to be reacted with the polyhydric alcohol is preferably a higher fatty acid having 8 to 18 carbon atoms, and examples thereof include caprylic acid, lauric acid, palmitic acid, and stearic acid. The addition mole number of ethylene oxide is preferably in the range of 5 to 40 mol. More specifically, for example, ethylene oxide adduct of glycerin monolaurate, ethylene oxide adduct of pentaerythritol, ethylene oxide adduct of sorbitan monolaurate, ethylene oxide adduct of sorbitan monostearate, pentaerythritol monolaurate Etc.
またこの本発明で用いる(B)成分としては、30℃での動粘度が5〜50mm2/sであることが非常に重要である。このような動粘度を満たすことにより、紡績時の集束性を高い状態に保つことが可能となったのである。動粘度が低い場合には集束性不良による糸バラケが多くなり糸切れの要因となり、逆に動粘度が高すぎる場合には繊維に付着した剤の粘性が高くなり、ゴムや金属ローラに捲き付きやすいという問題が起こる。 As the component (B) used in the present invention, it is very important that the kinematic viscosity at 30 ° C. is 5 to 50 mm 2 / s. By satisfying such a kinematic viscosity, it is possible to maintain high convergence during spinning. If the kinematic viscosity is low, the yarn breakage due to poor convergence will increase and cause thread breakage. Conversely, if the kinematic viscosity is too high, the viscosity of the agent adhering to the fiber will increase and stick to rubber or metal rollers. The problem is easy.
この(B)成分である多価アルコールのアルキレンオキサイド付加物は、本発明の短繊維表面に存在する油剤中に、5〜20重量%の範囲で含有することが必要である。5重量%未満ではスライバーの集束性の効果が低下し、単糸間のバラケが多くなり、スライバーの太さ斑が発生し、均一な紡績糸を得ることはできない。一方、20重量%を越えると集束性は良好であるものの油剤の粘性が増大し、高速練条や超高速空気革新精紡機(MTS、MJS等)の、ゴムローラー表面に油剤が堆積し、スライバーがゴムローラーに捲付くために、安定生産を行うことができない。 The alkylene oxide adduct of polyhydric alcohol as the component (B) needs to be contained in the range of 5 to 20% by weight in the oil agent present on the surface of the short fiber of the present invention. If it is less than 5% by weight, the effect of the sliver's converging property is reduced, and the variation between single yarns increases. On the other hand, if it exceeds 20% by weight, the convergence of the oil agent is good, but the viscosity of the oil agent increases, and the oil agent accumulates on the surface of the rubber roller of a high-speed kneading or ultra-high speed air revolutionary spinning machine (MTS, MJS, etc.). Since it sticks to the rubber roller, stable production cannot be performed.
そして本発明では上記(A)成分と(B)成分を規定量含有することに加え、高濃度油剤エマルジョン粘度が50Pa・s以下の油剤であることが必須である。高濃度とは20重量%以上の濃度をいい、さらには濃度が20〜70重量%のすべての範囲において油剤のエマルジョン粘度が50Pa・s以下であることが好ましい。さらには10〜40Pa・sのエマルジョン粘度を保つことが好ましい。このように高濃度であってもエマルジョン粘度を低く保つことにより、繊維表面に付着した後の様々な工程において有効に油剤の効果を発揮することが可能となる。紡績工程での工程通過性を良好させることが可能となったのであり、低湿から高湿までの様々な環境下において、ロール等への巻付きやスカムの発生を有効に防止しえたのである。なおここでいう高濃度油剤エマルジョン粘度は、所定の濃度に調整した後、B型粘度計を用い、30℃に調整した油剤エマルジョン中で円筒または円盤を回転させたときに、円筒・円盤間に働く液体の粘性抵抗トルクを測定したものである。 And in this invention, in addition to containing the said (A) component and (B) component in a defined amount, it is essential that it is an oil agent whose high concentration oil agent emulsion viscosity is 50 Pa.s or less. The high concentration means a concentration of 20% by weight or more, and the emulsion viscosity of the oil agent is preferably 50 Pa · s or less in the whole range of the concentration of 20 to 70% by weight. Furthermore, it is preferable to maintain an emulsion viscosity of 10 to 40 Pa · s. By keeping the emulsion viscosity low even at such a high concentration, it is possible to effectively exhibit the effect of the oil agent in various processes after adhering to the fiber surface. It has become possible to improve the process passability in the spinning process and effectively prevent winding around rolls and the occurrence of scum under various environments from low humidity to high humidity. The viscosity of the high-concentration oil emulsion referred to here is adjusted between the cylinder and the disk when the cylinder or disk is rotated in the oil emulsion adjusted to 30 ° C. using a B-type viscometer after adjusting to a predetermined concentration. This is a measurement of the viscous resistance torque of a working liquid.
また本発明の芳香族ポリアミド短繊維の表面に存在する油剤には、上記の(A)成分及び(B)成分以外に、通常の短繊維用油剤に使用されているアニオン界面活性剤や、ノニオン界面活性剤、さらには乳化調整剤、抗菌剤、防腐剤、紫外線吸収剤等を、本発明の目的を損なわない範囲で適宜選択使用することも好ましい。 In addition to the above-mentioned components (A) and (B), the oil present on the surface of the aromatic polyamide short fiber of the present invention includes anionic surfactants and nonions used in ordinary oils for short fibers. It is also preferable to appropriately select and use a surfactant, further an emulsification regulator, an antibacterial agent, an antiseptic, an ultraviolet absorber, and the like as long as the object of the present invention is not impaired.
本発明の芳香族ポリアミド短繊維は、上記の成分からなる油剤が付着したものであるが、その油剤の付着量としては、繊維重量に対して0.2〜1.0重量%であることが好ましい。その付着方法は特に限定する必要はないが、例えば、油剤を1〜10%の水溶液として、ローラ法、浸漬法、飛沫を塗布するスプレー法等の任意の方法により、紡糸、延伸等任意の段階で付与することができる。処理剤の付着量は、繊維に対して0.2〜1.0重量%、さらには0.3から0.8重量%とすることが望ましい。本発明で用いる油剤はその高濃度のエマルジョン粘度が低く保たれているため、工程途中の金属ロール上などにスカムが発生するなどの問題点を克服できたのである。 The aromatic polyamide short fiber of the present invention is one to which an oil agent composed of the above components is attached, and the amount of the oil agent to be attached is 0.2 to 1.0% by weight based on the fiber weight. preferable. The adhesion method is not particularly limited. For example, the oil agent is made into an aqueous solution of 1 to 10%, and an arbitrary step such as spinning and drawing by an arbitrary method such as a roller method, a dipping method, or a spray method for applying droplets. Can be granted. The adhesion amount of the treatment agent is preferably 0.2 to 1.0% by weight, more preferably 0.3 to 0.8% by weight with respect to the fiber. Since the oil agent used in the present invention has a low viscosity of the high-concentration emulsion, problems such as the occurrence of scum on the metal roll during the process can be overcome.
また本発明の芳香族ポリアミド短繊維は、後の加工が行いやすいように捲縮をかけたものであることが好ましく、捲縮数としては6〜15個/25mm、捲縮率としては7.5〜19%の範囲であることが好ましい。 The aromatic polyamide short fibers of the present invention are preferably crimped so that subsequent processing can be easily performed, the number of crimps is 6 to 15 per 25 mm, and the crimp rate is 7. A range of 5 to 19% is preferable.
この本発明の芳香族ポリアミド短繊維は、特に低湿度の条件下において、捲付きやスカムの発生が極めて少なく安定した紡績性が得られる。これは低粘度の油剤が均一に斑無く付着し、低湿度下でも静電気の発生が少なくすることができたためであると考えられる。本発明の芳香族ポリアミド系短繊維は、カード工程、練条工程等の紡績工程における工程通過性が極めて優れているのである。 This aromatic polyamide short fiber of the present invention has a stable spinnability with extremely little wrinkles and scum, particularly under conditions of low humidity. This is presumably because the low viscosity oil agent was evenly adhered without unevenness and the generation of static electricity could be reduced even under low humidity. The aromatic polyamide short fibers of the present invention are extremely excellent in process passability in spinning processes such as a card process and a drawing process.
以下、実施例により本発明をさらに具体的に説明する。なお、実施例中の%はすべて重量%を示す。また夫々の評価は下記の方法に従った。 Hereinafter, the present invention will be described more specifically with reference to examples. In addition, all% in an Example shows weight%. Moreover, each evaluation followed the following method.
(1)カード通過性
25℃、65%RHの条件下で300ゲレン/ヤード(0.9144m)、12rpmでカードにかけ口出し時のコイラーチュ−ブ詰りおよびカレンダーロールとコイラー間でのスライバーの垂れを観察した。総合的に問題のないものを○とし、紡績性等が特に不良で円滑に加工できない場合を×、中間のものを△と判定した。
(1) Card passability Under conditions of 25 ° C. and 65% RH, 300 coiler / yard (0.9144 m), 12 rpm, the coiler tube is clogged and the sliver dripping is observed between the calender roll and the coiler. did. A case where there was no problem overall was rated as ◯, a case where the spinning property was particularly poor and smooth machining was not possible, and a middle case was judged as △.
(2)カード静電気発生量
25℃、45%RHの条件下で300ゲレン/ヤード(0.9144m)、12rpmでカードにかけドッファ−と引取ローラとの間でウェブから10cm離れた高さ(位置)で春日式静電気測定器で静電気量(キロボルト:kV)を測定した。
(2) Card Static Electricity Generation Height (position) 10 cm away from the web between the doffer and the take-up roller on the card at 12 rpm with 300 gelen / yard (0.9144 m) at 25 ° C. and 45% RH Then, the amount of static electricity (kilovolt: kV) was measured with a Kasuga type static electricity meter.
(3)練条通過性
また、練条工程における特性としては、25℃、湿度65%の条件下で300ゲレン/ヤード(0.9144m)を180m/分の紡速で練条機を3回通過させ、口出し時の練条ローラ詰りや練条ローラへの捲付きを観察し、総合的に良好なものを○とし、特に不良で円滑に練条工程を通過できないものを×、中間を△と判定した。
(3) Stretching property Further, as a characteristic in the stretching process, a stretching machine is run three times at a spinning speed of 300 gelen / yard (0.9144m) at 180m / min under conditions of 25 ° C and 65% humidity. Observe clogging roller and clogging on the drawing roller at the time of squeezing, and mark overall good ones as ◯, especially those that are poor and cannot pass smoothly through the knitting process, △ middle It was determined.
(4)高濃度エマルジョン粘度
油剤エマルジョンの濃度を、それぞれ20、30、40、50、60、70重量%に調整し、それぞれ30℃の恒温水槽に入れた後、2時間後にB型粘度計にて粘度を測定した。各測定値のうち最大粘度(Pa・s)を高濃度エマルジョン粘度とした。
(4) High Concentration Emulsion Viscosity The oil emulsion concentration was adjusted to 20, 30, 40, 50, 60, and 70% by weight, respectively, placed in a constant temperature water bath at 30 ° C. The viscosity was measured. Among the measured values, the maximum viscosity (Pa · s) was defined as the high-concentration emulsion viscosity.
[実施例1]
固有粘度1.8のポリメタフェニレンイソフタルアミドを塩化カルシュウム水溶液中に押し出し、凝固させ単繊維繊度2.2dtex、計14万dtexのトウとなし、これを水洗後3.2倍に沸水中で延伸し、ついで乾燥し340℃で熱処理し、表1記載の各油剤に再度浸漬し、クリンパ−に供給して、クリンパ−での絞り率を調整して油剤付着量を0.5%とした後、クリンパ−で捲縮性能を付与し、120℃で乾燥熱処理を行い、51mmの長さに切断し芳香族ポリアミド短繊維を得た。
短繊維は捲縮数12山/インチ(2.54cm)、捲縮度は19%であった。得られた短繊維の紡績性を評価した結果を表1に示す。
[Example 1]
Polymetaphenylene isophthalamide having an intrinsic viscosity of 1.8 is extruded into an aqueous solution of calcium chloride and solidified to form a single fiber fineness of 2.2 dtex and a total toe of 140,000 dtex, which is then washed 3.2 times in boiling water after washing with water. Then, after drying and heat-treating at 340 ° C., re-immersing in each oil listed in Table 1, supplying to the crimper, adjusting the squeezing rate in the crimper, and adjusting the oil adhesion amount to 0.5% Then, crimping performance was imparted with a crimper, a drying heat treatment was carried out at 120 ° C., and cut into a length of 51 mm to obtain an aromatic polyamide short fiber.
The short fiber had 12 crimps / inch (2.54 cm), and the crimp was 19%. Table 1 shows the results of evaluating the spinnability of the obtained short fibers.
[実施例2,3、比較例1〜3]
実施例1の油剤を表記載のように変更した以外は、実施例1と同じ条件にて芳香族ポリアミド短繊維を得た。得られた短繊維の紡績性を評価し、結果を表1に併せて示す。
[Examples 2 and 3, Comparative Examples 1 to 3]
Aromatic polyamide short fibers were obtained under the same conditions as in Example 1 except that the oil agent in Example 1 was changed as described in the table. The spinnability of the obtained short fibers was evaluated, and the results are also shown in Table 1.
Claims (5)
(A)炭素数が6〜12の燐酸エステルのアルカリ金属塩
(B)30℃での動粘度が5〜50mm2/sである多価アルコールのアルキレンオキサイド付加物。 An aromatic polyamide short fiber having an oil agent attached to the surface of the aromatic polyamide fiber, the oil agent containing 50 to 95% by weight of the component (A), 5 to 20% by weight of the component (B), and An aromatic polyamide short fiber, wherein the oil agent has a high-concentration emulsion viscosity of 50 Pa · s or less.
(A) Alkali metal salt of phosphate ester having 6 to 12 carbon atoms (B) Alkylene oxide adduct of polyhydric alcohol having a kinematic viscosity at 30 ° C. of 5 to 50 mm 2 / s.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010038805A JP5567363B2 (en) | 2010-02-24 | 2010-02-24 | Aromatic polyamide short fiber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010038805A JP5567363B2 (en) | 2010-02-24 | 2010-02-24 | Aromatic polyamide short fiber |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2011174198A true JP2011174198A (en) | 2011-09-08 |
JP5567363B2 JP5567363B2 (en) | 2014-08-06 |
Family
ID=44687300
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2010038805A Active JP5567363B2 (en) | 2010-02-24 | 2010-02-24 | Aromatic polyamide short fiber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP5567363B2 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5643910B1 (en) * | 2014-04-30 | 2014-12-17 | 松本油脂製薬株式会社 | Fiber treatment agent for short fibers and use thereof |
JP2019002093A (en) * | 2017-06-16 | 2019-01-10 | 松本油脂製薬株式会社 | Treatment agent for synthetic fiber and application thereof |
CN113981682A (en) * | 2021-10-26 | 2022-01-28 | 烟台泰和新材料股份有限公司 | Pre-activated para-aramid fiber and preparation method thereof |
CN114075784A (en) * | 2020-08-20 | 2022-02-22 | 中蓝晨光化工有限公司 | Secondary oil treatment method of heterocyclic aramid |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5846179A (en) * | 1981-09-10 | 1983-03-17 | 帝人株式会社 | Treating agent for aromatic polyamide synthetic fiber having excellent spinning property |
JPH042879A (en) * | 1990-04-13 | 1992-01-07 | Teijin Ltd | Aromatic polyamide staple fiber |
JP2002227076A (en) * | 2001-01-29 | 2002-08-14 | Teijin Ltd | Aromatic polyamide fiber |
-
2010
- 2010-02-24 JP JP2010038805A patent/JP5567363B2/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5846179A (en) * | 1981-09-10 | 1983-03-17 | 帝人株式会社 | Treating agent for aromatic polyamide synthetic fiber having excellent spinning property |
JPH042879A (en) * | 1990-04-13 | 1992-01-07 | Teijin Ltd | Aromatic polyamide staple fiber |
JP2002227076A (en) * | 2001-01-29 | 2002-08-14 | Teijin Ltd | Aromatic polyamide fiber |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5643910B1 (en) * | 2014-04-30 | 2014-12-17 | 松本油脂製薬株式会社 | Fiber treatment agent for short fibers and use thereof |
WO2015166603A1 (en) * | 2014-04-30 | 2015-11-05 | 松本油脂製薬株式会社 | Agent for treating short-staple fibers and use for said agent |
JP2016065322A (en) * | 2014-04-30 | 2016-04-28 | 松本油脂製薬株式会社 | Fiber treatment agent for short fiber and use thereof |
JP2019002093A (en) * | 2017-06-16 | 2019-01-10 | 松本油脂製薬株式会社 | Treatment agent for synthetic fiber and application thereof |
CN114075784A (en) * | 2020-08-20 | 2022-02-22 | 中蓝晨光化工有限公司 | Secondary oil treatment method of heterocyclic aramid |
CN114075784B (en) * | 2020-08-20 | 2023-08-08 | 中蓝晨光化工有限公司 | Secondary oiling agent treatment method for heterocyclic aramid fiber |
CN113981682A (en) * | 2021-10-26 | 2022-01-28 | 烟台泰和新材料股份有限公司 | Pre-activated para-aramid fiber and preparation method thereof |
CN113981682B (en) * | 2021-10-26 | 2023-09-05 | 泰和新材集团股份有限公司 | Preactivated para-aramid fiber and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JP5567363B2 (en) | 2014-08-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4612717B2 (en) | Composite fiber with excellent stretch and post-processing properties | |
WO2014024647A1 (en) | Processing agent for synthetic fibers and use thereof | |
JP5567363B2 (en) | Aromatic polyamide short fiber | |
JP2011174195A (en) | Aromatic polyamide staple fiber and spun yarn comprising the same | |
JP2011174197A (en) | Aromatic polyamide staple fiber | |
JP2009235647A (en) | Method for producing high-strength nylon 66 fiber for reinforcing rubber | |
JPH11229276A (en) | Polyester fiber having excellent processability | |
JP4584468B2 (en) | Aromatic polyamide fiber | |
JP4397935B2 (en) | Para-type aromatic polyamide short fiber | |
JP2012082535A (en) | Manufacturing method of aromatic polyamide staple fiber for nonwoven fabric | |
JP2011074546A (en) | Staple fiber of aromatic polyamide, and method of producing the same | |
JPS63112769A (en) | Polyester staple fiber | |
JP2011174196A (en) | Aromatic polyamide staple fiber and spun yarn comprising the same | |
JP2011089235A (en) | Aromatic polyamide staple fiber and spun yarn comprising the same | |
WO2019208404A1 (en) | Polyamide monofilament | |
JPH0418169A (en) | Lubricant for fiber treatment | |
JP3856612B2 (en) | Totally aromatic polyamide short fiber | |
CN100537887C (en) | Contraposition aromatic polyamide staple fibre | |
JP2011127239A (en) | Aromatic polyamide staple fiber and spun yarn comprising the same | |
JP2021143433A (en) | Polyester false twisted yarn | |
JP2505570B2 (en) | Polyester fiber | |
JP4367198B2 (en) | Polyester fiber | |
JP3720162B2 (en) | Treatment agent for synthetic fibers | |
KR101427835B1 (en) | Process for the preparing polyamide staple fiber having excellent spinability | |
JP2019173188A (en) | Aromatic polyamide fiber and fabric containing the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
RD02 | Notification of acceptance of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7422 Effective date: 20110630 |
|
RD04 | Notification of resignation of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7424 Effective date: 20110630 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20121116 |
|
A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A712 Effective date: 20121116 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20130624 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130702 |
|
A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130826 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130924 |
|
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: 20140527 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20140619 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5567363 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |