JPH0242938B2 - - Google Patents
Info
- Publication number
- JPH0242938B2 JPH0242938B2 JP3330183A JP3330183A JPH0242938B2 JP H0242938 B2 JPH0242938 B2 JP H0242938B2 JP 3330183 A JP3330183 A JP 3330183A JP 3330183 A JP3330183 A JP 3330183A JP H0242938 B2 JPH0242938 B2 JP H0242938B2
- Authority
- JP
- Japan
- Prior art keywords
- fine particles
- fiber
- plasma
- attached
- fiber surface
- 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
Links
- 239000000835 fiber Substances 0.000 claims description 132
- 239000010419 fine particle Substances 0.000 claims description 97
- 229920000642 polymer Polymers 0.000 claims description 34
- 239000011159 matrix material Substances 0.000 claims description 16
- 238000004519 manufacturing process Methods 0.000 claims description 12
- 239000000758 substrate Substances 0.000 claims description 10
- 239000011164 primary particle Substances 0.000 claims description 7
- 230000001678 irradiating effect Effects 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 150000002739 metals Chemical class 0.000 claims description 3
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 3
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 3
- 230000000737 periodic effect Effects 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 125000000123 silicon containing inorganic group Chemical group 0.000 claims description 3
- ZCUFMDLYAMJYST-UHFFFAOYSA-N thorium dioxide Chemical compound O=[Th]=O ZCUFMDLYAMJYST-UHFFFAOYSA-N 0.000 claims description 3
- 229910003452 thorium oxide Inorganic materials 0.000 claims description 3
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- 239000011362 coarse particle Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 description 41
- 238000000034 method Methods 0.000 description 27
- 229920002994 synthetic fiber Polymers 0.000 description 26
- 239000012209 synthetic fiber Substances 0.000 description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 23
- 239000004744 fabric Substances 0.000 description 20
- 229920000728 polyester Polymers 0.000 description 20
- 239000004840 adhesive resin Substances 0.000 description 16
- 229920006223 adhesive resin Polymers 0.000 description 16
- -1 that is Polymers 0.000 description 11
- 238000011161 development Methods 0.000 description 10
- 239000007789 gas Substances 0.000 description 10
- 239000000377 silicon dioxide Substances 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- 238000005516 engineering process Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 229920000139 polyethylene terephthalate Polymers 0.000 description 8
- 239000005020 polyethylene terephthalate Substances 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000003513 alkali Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 238000010586 diagram Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- 208000016261 weight loss Diseases 0.000 description 6
- 239000008119 colloidal silica Substances 0.000 description 5
- 238000004043 dyeing Methods 0.000 description 5
- 229920000307 polymer substrate Polymers 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 238000007788 roughening Methods 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- 210000002268 wool Anatomy 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 238000004040 coloring Methods 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 238000005530 etching Methods 0.000 description 4
- 210000003746 feather Anatomy 0.000 description 4
- 239000002657 fibrous material Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 238000009832 plasma treatment Methods 0.000 description 4
- 239000013585 weight reducing agent Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical group OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 150000002334 glycols Chemical class 0.000 description 3
- 230000001771 impaired effect Effects 0.000 description 3
- 239000002932 luster Substances 0.000 description 3
- 239000011859 microparticle Substances 0.000 description 3
- 238000001020 plasma etching Methods 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
- 239000002344 surface layer Substances 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000003570 air Substances 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000006224 matting agent Substances 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- YZTJKOLMWJNVFH-UHFFFAOYSA-N 2-sulfobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O YZTJKOLMWJNVFH-UHFFFAOYSA-N 0.000 description 1
- CARJPEPCULYFFP-UHFFFAOYSA-N 5-Sulfo-1,3-benzenedicarboxylic acid Chemical group OC(=O)C1=CC(C(O)=O)=CC(S(O)(=O)=O)=C1 CARJPEPCULYFFP-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004705 High-molecular-weight polyethylene Substances 0.000 description 1
- 241000234435 Lilium Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
- 241000237502 Ostreidae Species 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000872198 Serjania polyphylla Species 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000002270 dispersing agent 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
- 238000001035 drying Methods 0.000 description 1
- 238000000635 electron micrograph Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 235000020636 oyster Nutrition 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
Description
本発明は粗面化された繊維構造物、およびその
製造方法に関し、殊に染色物の色の深みを画期的
に向上させると共に、絹以上のきしみ感を有する
新規な風合をも繊維構造物に関する発明である。
尚本発明は、繊維表面の粗面化技術に関するも
のであるが、この発明が、殊にポリエステル合成
繊維で代表される溶融紡糸された疎水性合成繊維
に適用したときの発色性並びに風合の向上効果が
著るしいため、この明細書では合成繊維の発色性
並びに風合の向上効果に例をとつて記載されてい
る。しかし以下で容易に理解されるように、本発
明の原理は、合成繊維の発色性並びに風合改良に
とどまらず、繊維一般の表面粗面化技術という点
でポリエステル合成繊維以外の合成繊維は無論の
こと、天然繊維にも適用出来るものであることは
明らかである。
各種繊維の色の深みを増す技術や風合を改良す
る技術は種々検討されているが、あらゆる繊維に
応用できる技術は確立されておらず、そのような
技術が待望されていた。
又従来各種有機合成繊維特に溶融紡糸された合
成繊維は、その繊維表面の滑らかさのため特有の
ワキシー感、鏡面光沢があり、かつ羊毛や絹等に
くらべて色の深みが得られないなどの欠点を有し
ていた。
通常、繊維表面を粗にすることが光沢の改良や
風合い変化の手段となると考えられ、微粒子、例
えば酸化チタンを添加して艶を消すことが行なわ
れるが、この方法では単に艶を消すのみで発色性
が悪くなることはよく知られている。
この発色性、とりわけ色の深み、鮮明度は、繊
維の如何なる使用分野への素材条件としても必要
なものであるが、特にフオーマルウエアの如き黒
染品としては必須であり、この黒色の染色物にお
いて色の深みがありかつ鮮明さがある黒染品が得
られにくいというのが実情であつた。
そして特にポリエステル系合成繊維は、その優
れた機能性のために最も多く使用されているが、
前述の如き発色性の点で解決すべき点があり、色
の深みや鮮明度に優れたものが特に要望されると
ころであつた。
合成繊維の前記問題点を解決するために各種の
技術が公けにされている。
本発明者等も先に無機微粒子を含有するポリエ
ステル繊維をアルカリエツチングして繊維表面に
特定の凹凸を形成させ、該凹凸粗面により濃色化
効果を得る技術につき特開昭55−107512号などで
提案した。
また先輩研究者等により、有機合成繊維にグロ
ー放電プラズマを照射し、繊維表面に特定の凹凸
を形成させ、この凹凸により濃色化効果を得る技
術も特開昭52−99400号として公けにされている。
前者は従来のポリエステル繊維では達成し得な
かつた優れた濃色化効果を付与出来る技術と自負
しているが、難点は光沢が減少し、光沢のある濃
色効果が得られにくいものである。
又後者は、製造手段の点で本発明の土台となる
ものであるが、通常の合成繊維、即ち、微粒子を
含有しない合成繊維にプラズマ照射する技術に関
するものであり、得られた合成繊維においてはそ
れなりに発色性が向上するが、前記前者で得られ
る繊維に比べても、いまだ満足のゆくものではな
く、さらに処理時間が長く必要であり、処理スピ
ードがあがらずコスト的に問題があつた。
これ等先行公知技術に対して、本発明者等は、
先に、プラズマに対する遮蔽手段となる微粒子を
合成繊維にできるだけ多く、均一に分散・含有さ
せておき、その微粒子を分散・含有させた合成繊
維に低温プラズマ照射を行なうことによつて、微
粒子で遮蔽されない基質ポリマー部分はプラズマ
でエツチングされて凹部を形成し、微粒子で遮蔽
された基質ポリマー部分は該微粒子と共にエツチ
ングされずに凸部を形成し、結果として繊維表面
に微細な多数の凹凸構造を形成させる発明につき
提案した。
この発明(以下先願と記す)は、前記第1の公
知技術とは製造手段の違いにより、さらに格段に
すばらしい光沢のある色の深み、色の鮮明性を付
与できる発明であり、又前記第2の公知技術に対
しても、得られる濃色向上効果は全く予想もでき
ないほど格段に優れたものである。しかしこの先
願も、また前記第1の公知技術で得られる製品
も、製品の摩擦耐久性に関して、いまだ充分満足
できるものではなかつた。又製造プロセス上で
も、先願は、微粒子の凝集を回避し、ポリマー中
へ微粒子を均一かつ多量に分散・含有させたポリ
マーを作成し、かつ該ポリマーから実用性のある
繊維を製造することは種々の制約と高度な技術を
要し、また合成繊維にのみ適用できるものであ
る。さらにまたこの方式は、繊維表面に凹凸を形
成するためのプラズマ照射時間を、より短縮する
必要があつた。
本発明は、前記第1、第2の公知技術に対する
先願発明の効果と同じ効果を有すると共に、さら
に先願発明の前記の不満足点をも解決した発明に
関するものである。
即ち本発明の第1の発明は、低温プラズマ中で
繊維を構成するポリマー基質に比しより不活性で
ある微粒子を繊維表面に付着させた繊維構造物に
プラズマ照射してなる繊維構造物であつて、ポリ
マー基質の微粒子で遮蔽されない部分はプラズマ
でエツチングされて凹部を形成し、微粒子で遮蔽
された部分は微粒子と共にエツチングされずに凸
部を形成して繊維表面上に凹凸を形成しており、
該凹凸は互いに隣接する凸部間の中心間距離が
0.01ないし1ミクロンであり、該凸部が1平方ミ
クロン当たり1ないし200個存在している粗面化
された繊維構造物である。
又第2の発明は、低温プラズマ中で繊維を構成
するポリマー基質に比しより不活性である平均一
次粒子径が0.5μ以下の微粒子を繊維表面に繊維に
対して0.01ないし10重量%付着させる工程、該微
粒子を付着させた繊維構造物に低温プラズマ照射
を行なう工程、を包含する繊維表面上に凹凸を形
成させる粗面化された繊維構造物の製造方法であ
る。
本発明者は、本発明で得られる繊維構造物の効
果が前記で先願として示した微粒子含有繊維構造
物にプラズマ照射して得られた構造物の効果に比
し摩擦耐久性が優れ、かつ絹以上のきしみ感のあ
る風合を有し、さらにまた発色性に優れている点
については、そのメカニズムを充分に解明してい
ない。しかし本発明と先願との差は次のように説
明されると考えている。
本発明の原理は第1図a,bの模式図で説明さ
れる。1は繊維の表層部分であり、2は繊維の表
面を被覆し、付着された微粒子である。本発明の
繊維は、第1図aで示される繊維にプラズマを照
射することによつて第1図bで示されるように、
微粒子で被覆されたポリマー基質部分はエツチン
グされずに残り、微粒子で被覆されなかつたポリ
マー基質部分が均一な深さにエツチングされるこ
とを示している。本発明で注目すべきは、付着さ
せる微粒子がポリマー基質部分に対してほぼ同一
高さの位置に位置していることであり、これによ
りエツチングされずに残つた微粒子の位置からエ
ツチングされて凹部となつた基質表面までの深さ
Dが、いずれの凹部でもほぼ均一な深さ(逆に言
えばいずれの凸部でもほぼ均一な高さ)を形成し
ていることである。
これに対して第2図a,bは先願の場合の例
で、繊維ポリマー基質中へ微粒子2′を分散含有
させた繊維aに、プラズマ照射したb場合の模式
図である。この場合には、微粒子はポリマー基質
中へ分散させたものであるため、微粒子はポリマ
ー基質中で高さが不揃いで位置している。従つて
このような繊維にプラズマ照射すれば、プラズマ
照射によつて繊維表面に出てくる微粒子の位置か
ら、微粒子がなくなつてエツチングされて凹部と
なつた基質表面までの深さDは、不揃いである。
また微粒子の位置が不揃いであることと、微粒子
より表層に位置するポリマー基質はプラズマ照射
によりエツチングされて飛散するから前記本発明
の場合に比較して、同一のプラズマ照射時間で比
較すると平均的な凹部の深さ(逆に表現すれば凸
部の高さ)は小さくなる。
即ち、形成される凹凸が均一な深さ(高さ)と
なりかつその深さ(高さ)もより充分な深さ(高
さ)を有するために摩擦耐久性、風合い、発色性
を満足したものが得られる、と考えられる。
本発明の対象は、前述のように合成繊維に限ら
れず、ウール、綿、麻、絹等の天然繊維、アセテ
ート等の半合成繊維およびレーヨン等の再生繊維
をも包含するものである。合成繊維としては、ポ
リエステル系、ポリアミド系、アクリル系、ポリ
ウレタン系、その他の合成繊維を包含意味する
が、該合成繊維はその一部が共重合されたものあ
るいは2成分のブレンド、貼り合わせのものでも
よい。又界面活性剤やつや消し剤、顔料等を含ん
でいてもよい。
本発明の繊維構造物は、上述の繊維の単独ある
いは2種以上の繊維を複合・混合して構成された
ものを包含し、トウ、フイラメント、ヤーン等の
糸条物に限られるものでなく、当然のことながら
該糸条物を編織してなる編物や織物でもよく、又
不織布でもよく、あらゆる形態の布状二次元物を
包含意味するものである。
繊維基質表面に存在する微粒子からなる凸部
は、繊維表面を走査型電子顕微鏡で1万倍以上に
拡大して写つた写真で観察・測定され、繊維表面
に0.01ないし1ミクロンの凹凸がその効果上有効
なことがわかつた。ここでこの凹凸とは、上記電
子顕微鏡写真で繊維軸方向に沿つて凸部の中心
(あるいは中心付近)と隣の凸部の中心(あるい
は中心付近)までの距離を約30個場所を変えて測
定し、平均した値である。
この値が0.01ミクロンより小さいと染色物の濃
色効果は少なく、逆に1ミクロンより大きくなる
とやはり濃色効果がない。したがつて該凹凸は
0.01〜1ミクロンの範囲のものが好ましく、0.1
〜0.5ミクロンのものがさらに好ましい。
又この凹凸は、個数でいえば1平方ミクロン当
り1〜200個存在していることが好ましい。この
個数の測定も繊維表面を走査型電子顕微鏡で1万
倍以上に拡大して写つた写真で、一辺を1ミクロ
ンとする正方形内に存在する凸部の個数を数えた
ものである。この個数が200個以上になると凹凸
の形状が小さくなりすぎて濃色化効果は小さい。
好ましくは3〜100個である。
製造方法としては、本発明は、まず繊維構造物
の繊維表面上に微粒子を付着させること、つぎに
その微粒子を付着させた繊維構造物を染色前ある
いは染色後低温プラズマ処理すること、によつて
得られる。
本発明における微粒子は、低温プラズマ中でポ
リマー基質に比し、より不活性であることが重要
であり、含ケイ素無機粒子、周期律表第族金属
の酸化物およびまたはその塩類からなる無機微粒
子、酸化アルミニウム、酸化トリウムおよび酸化
ジルコニウムからなる群から選ばれる平均の一次
粒子径が0.5ミクロンより小さい微粒子が用いら
れ、より好ましくは0.2ミクロン以下、さらに好
ましくは0.07ミクロン以下のものが用いられる。
0.07ミクロン以下、0.03ミクロン以上では低温プ
ラズマ照射した染色物はやや青味をおび、0.03ミ
クロン以下ではやや赤味をおびる傾向がうかがわ
れる。
さらに又凹部は、前述のように微粒子がプラズ
マ照射によつても飛ばされずに残り、その残つた
微粒子を核としてポリマー基質が粒状形態になつ
たものと思われるので、したがつて凸部を構成す
る微粒子の種類そのものも濃色化効果に影響し、
前述した微粒子の内でも屈折率の低いものが好ま
しく、この点でシリカが最も好ましい。
微粒子としてはその分散性などから、できれば
コロイド状に分散させたものが使用しやすいが、
これに限定されるものではない。
微粒子を繊維表面に付与する方法は通常行なわ
れている樹脂加工方法を採用することができる。
例えば樹脂液をパツデイング、スプレ、印捺など
の方法により繊維構造物に付与した後マングルな
どで適宜の付着量に調整した後、乾熱あるいは湿
熱処理することによつて繊維表面に付着される。
微粒子と繊維の接着性を強固にしたい場合に
は、微粒子を付着させる時に同時に、または微粒
子を付着した後に接着性樹脂を付着させることが
できる。この接着性樹脂としては水分散エマルジ
ヨンのものが使用しやすく、微粒子と同時に付着
させる場合は微粒子のコロイド状物と混合時に互
いに凝集しない組合わせのものであればよい。例
えば微粒子としてコロイダルシリカを用いる場
合、樹脂エマルジヨンとしては一般的にカチオン
系のものはコロイダルシリカと凝集しやすいの
で、アニオン系またはノニオン系のものが好まし
い。無論微粒子と接着性樹脂との混合系に帯電防
止剤などの仕上剤を含有させてもよく、また微粒
子付着後に接着性樹脂をつける場合には、これら
仕上剤は、どちらに含有させてもよい。ただ微粒
子量に対して必要以上の接着性樹脂を与えると、
本発明の優れたきしみ感を損なう結果となりやす
いので、微粒子量に対して接着性樹脂量の比が1
より小となるようにすることが望ましい。
また微粒子の繊維に対する接着性を付与する方
法として、微粒子付着後プラズマ照射し、その後
接着性樹脂を付着させる方法も有効である。この
方法の1つとして接着性樹脂をプラズマ重合で付
着させる方法がある。この方法は耐久性を著るし
く向上させることが可能であると同時に、工程
が、低温プラズマ照射−プラズマ重合というドラ
イプロセスで処理できる利点がある。プラズマ重
合により樹脂を形成させる方法としては、プラズ
マエツチング終了後ラジカルを残留させた状態で
モノマーを導入させる方法及びプラズマエツチン
グ後さらに放電状態下にモノマーを導入してプラ
ズマ重合させる2つの方法がある。このプラズマ
重合できる接着性樹脂としては、沸点が比較的低
く常温で揮発性のものが好ましい。このようなも
のとしてはアクリル酸、メタアクリル酸またはこ
れらのエステル、ケイ素化合物、フツ素化合物等
がある。
前に触れたように、本発明の凹凸部形成のメカ
ニズムは、ポリマー基質の、微粒子で遮蔽されな
い表面部分はプラズマ照射により飛散し凹部を形
成するが、基質表面に付着させた微粒子はプラズ
マ照射によつても飛散することなく基質表面に残
り、かつ該微粒子によつて遮蔽された基質部分が
残ることによつて、該微粒子を核とした凸部が形
成されるものと思われる。即ち、基質表面上に付
着させた微粒子は基質に対する遮蔽物となつてお
り、その遮蔽物がない部分がプラズマにより基質
内部へ順次エツチングされていくものと思われ
る。したがつて上記考えに立てば、繊維表面に、
多くの、限られたサイズの凹凸部を形成させるた
めには、繊維基質表面上にできるだけ均一に、で
きるだけ多くの微粒子を存在させることが極めて
重要であると考えられる。しかしそれと共に、遮
蔽物となる微粒子の層が必要以上に厚くては基質
内部へのエツチングが阻害されまた風合が損なわ
れるので、できるだけ薄い膜状態となつているこ
とが好ましい。その点で、微粒子の繊維表面上へ
の付着量は繊維に対して0.01〜10重量、より好ま
しくは0.05〜2重量%とするのがよい。付着量が
0.01%より少なくなると発色性並びに風合改良効
果が小さく、10%を越えると風合が著るしく損な
われてくる。
プラズマとは、物質に高いエネルギーが与えら
れて、分子または原子が解離し、中性原子のほか
に陽イオンとこれにほぼ釣合つた数の陰イオンま
たは電子を含んだ気体となつた状態を言う。通常
低温プラズマは10Torr以下の減圧下のガス雰囲
気に低周波、高周波あるいはマイクロ波による高
電圧を印加することによつて発生させる。この発
生させられた励起原子、イオン、電子等がポリマ
ー基質表面に作用し、表面をエツチングするもの
である。低温プラズマを発生させるためのガスと
しては、例えば酸素、空気、窒素、アルゴン、オ
レフイン等が好ましく用いられる。
低温プラズマ処理の条件は、対象となる繊維の
材質、組成、形状および目的とする濃色度合によ
つて装置のタイプ、形状、ガスの種類、流量、真
空度、出力および処理時間等を適宜選択する必要
がある。例えば、本発明で得られる物品は、繊維
構造物の表面および裏面の全体にわたつて凹凸化
されていることは必ずしも必要ではなく、場合に
よつては片面のみでよい。したがつてその場合に
は片面に出ている繊維表面が凹凸化されればよい
ものであり、その点は適宜プラズマ処理条件を選
択して行なわれる。又低温プラズマを発生させる
ために用いるガスとして空気、酸素、アルゴンに
ついていえば、濃色化効果の点からは酸素>空気
>アルゴンの順であり、用いるガスの種類も効果
に影響のあることがわかつた。またガスの流量に
ついても真空度が一定となるように保つて流量を
変化させてみると、ガス流量がエツチング速度が
大きな影響を及ぼすことがわかつた。
又プラズマ処理自体は繊維の染色前あるいは染
色後いずれでもよいが、染色前に行なう方法はそ
の後染色工程を程る際に繊維表面に形成された凹
凸が変形される可能性があり、その点の恐れのな
い染色後に行なう方が好ましい。
又本発明は、繊維構造物の照射面の一部を前記
付着微粒子とは別の被覆物でもつて被覆し、プラ
ズマ照射される部分とされない部分とをつくつて
低温プラズマ照射を行なうことにより、被覆した
部分の模様や色を被覆していない部分の模様や色
とかえることができる。そしてこの方法における
被覆部と非被覆部との境界は非常に鮮明であり、
染色物にめずらしい効果を付与することができ
る。
又本発においては、微粒子を付着させる対象の
繊維構造物としては、繊維が予め粗面化された繊
維からなる構造物を用いることができる。この予
め粗面化された繊維からなる繊維構造物として
は、例えば前記で第1公知例として示した予め微
粒子を含有させたポリエステル繊維をアルカリ液
でエツチング処理して繊維表面に特定の凹凸を形
成させたポリエステル繊維からなる構造物、ある
いはさらに前記で先願例として示した予め微粒子
を含有させた合成繊維をプラズマエツチングして
繊維表面に特定の凹凸を形成させた合成繊維から
なる繊維構造物等が代表的な例として挙げられる
が、これら粗面化繊維構造物に限定されるもので
はない。
合成繊維中ポリエステル系繊維は、最も染色物
の色の深み、鮮明度が劣るが、本発明の技術は上
記のようにポリエステル繊維に対して濃色化度合
の向上効果が著しいものであり、ポリエステル繊
維に対して特にその効果を発揮出来る技術である
と言える。この場合のポリエステル系ポリマーと
は、繰返し構造単位の少なくとも約75%が
The present invention relates to a fiber structure with a roughened surface and a method for producing the same, and in particular to a fiber structure that dramatically improves the depth of color of dyed products, and also provides a new texture with a more squeaky feel than silk. It is an invention related to things. The present invention relates to a technology for roughening the surface of fibers, and this invention particularly improves the color development and texture when applied to melt-spun hydrophobic synthetic fibers such as polyester synthetic fibers. Since the improvement effect is remarkable, this specification describes the improvement effect on the coloring properties and hand of synthetic fibers as an example. However, as will be easily understood below, the principle of the present invention is not limited to improving the color development and texture of synthetic fibers, but also applies to synthetic fibers other than polyester synthetic fibers in terms of surface roughening technology for fibers in general. It is clear that this can also be applied to natural fibers. Although various techniques for increasing the depth of color and improving the texture of various fibers have been studied, no technology has been established that can be applied to all types of fibers, and such a technology has been long-awaited. Conventionally, various organic synthetic fibers, especially melt-spun synthetic fibers, have a unique waxy feel and mirror gloss due to the smoothness of their fiber surfaces, and they have problems such as not being able to obtain the depth of color compared to wool, silk, etc. It had drawbacks. Normally, roughening the fiber surface is thought to be a means of improving gloss or changing the texture, and fine particles such as titanium oxide are added to eliminate the luster, but this method only eliminates the luster. It is well known that color development deteriorates. This color development, especially the depth and clarity of the color, is necessary as a material condition for any field of use of textiles, but it is especially essential for black-dyed products such as formal wear. The reality is that it is difficult to obtain black-dyed products with deep color and clarity. In particular, polyester synthetic fibers are the most commonly used due to their excellent functionality.
As mentioned above, there are problems to be solved in terms of color development, and there has been a particular demand for products with excellent color depth and clarity. Various techniques have been published to solve the above-mentioned problems with synthetic fibers. The present inventors have also previously published a technique in which a polyester fiber containing inorganic fine particles is etched with alkali to form specific irregularities on the fiber surface, and the uneven rough surface produces a darkening effect, such as in JP-A No. 55-107512. I proposed it. In addition, senior researchers published a technique in JP-A No. 52-99400, in which organic synthetic fibers are irradiated with glow discharge plasma to form specific irregularities on the fiber surface, and these irregularities produce a darkening effect. has been done. The former is a technology that can provide an excellent darkening effect that cannot be achieved with conventional polyester fibers, but the drawback is that the gloss decreases, making it difficult to obtain a glossy darkening effect. The latter, which forms the basis of the present invention in terms of manufacturing means, relates to a technique of plasma irradiation to ordinary synthetic fibers, that is, synthetic fibers that do not contain fine particles, and the resulting synthetic fibers Although the color development property is improved to a certain degree, it is still not satisfactory compared to the fiber obtained by the former method, and furthermore, the processing time is longer, and the processing speed is not increased, which poses a problem in terms of cost. Regarding these prior art, the present inventors
First, fine particles that serve as a means of shielding against plasma are uniformly dispersed and contained in synthetic fibers as much as possible, and the synthetic fibers in which the fine particles are dispersed and contained are irradiated with low-temperature plasma. The parts of the matrix polymer that are not etched are etched by plasma to form recesses, and the parts of the matrix polymer that are shielded by the fine particles are not etched together with the fine particles and form convex parts, resulting in the formation of a large number of fine uneven structures on the fiber surface. proposed an invention that would This invention (hereinafter referred to as the "prior application") is an invention that can provide even more excellent glossy color depth and color clarity due to the difference in manufacturing method from the above-mentioned first known technology. Even with respect to the known technique No. 2, the effect of improving the deep color obtained is far more excellent than could have been expected. However, neither this prior application nor the products obtained by the first known technique are yet fully satisfactory with respect to the friction durability of the products. In addition, in terms of the manufacturing process, the previous application disclosed that it was possible to avoid agglomeration of fine particles, create a polymer in which fine particles were uniformly dispersed and contained in a large amount, and manufacture practical fibers from the polymer. It requires various restrictions and advanced technology, and can only be applied to synthetic fibers. Furthermore, in this method, it was necessary to further shorten the plasma irradiation time for forming irregularities on the fiber surface. The present invention relates to an invention that has the same effect as the earlier invention with respect to the first and second known techniques, and also solves the above-mentioned unsatisfactory points of the earlier invention. That is, the first aspect of the present invention is a fiber structure obtained by irradiating a fiber structure with fine particles, which are more inert than the polymer matrix constituting the fiber, attached to the fiber surface in a low-temperature plasma, and Therefore, the parts of the polymer matrix that are not shielded by the fine particles are etched by the plasma and form concave parts, and the parts that are shielded by the fine particles are not etched together with the fine particles and form convex parts, forming unevenness on the fiber surface. ,
The unevenness is such that the distance between the centers of adjacent protrusions is
It is a roughened fibrous structure having a diameter of 0.01 to 1 micron and 1 to 200 protrusions per square micron. The second invention is to attach 0.01 to 10% by weight of fine particles with an average primary particle size of 0.5μ or less to the fiber surface, which are more inert than the polymer matrix constituting the fiber in low-temperature plasma. This is a method for producing a roughened fibrous structure in which unevenness is formed on the fiber surface, including a step of irradiating the fibrous structure with the fine particles adhered to low-temperature plasma. The present inventor has discovered that the effect of the fiber structure obtained by the present invention is superior in friction durability compared to the effect of the structure obtained by plasma irradiation on the fine particle-containing fiber structure shown in the earlier application, and The mechanism behind the fact that it has a texture that is more squeaky than silk and has excellent color development has not been fully elucidated. However, we believe that the difference between the present invention and the prior application can be explained as follows. The principle of the invention is illustrated by the schematic diagrams in FIGS. 1a and 1b. 1 is a surface layer portion of the fiber, and 2 is a fine particle that covers and adheres to the surface of the fiber. The fibers of the present invention can be produced as shown in FIG. 1b by irradiating the fibers shown in FIG. 1a with plasma.
The portions of the polymer substrate that were coated with microparticles remained unetched, indicating that the portions of the polymer substrate that were not coated with microparticles were etched to a uniform depth. What should be noted in the present invention is that the fine particles to be deposited are located at almost the same height with respect to the polymer matrix portion, and as a result, the fine particles that remain unetched are etched from the position and form the recesses. The depth D to the surface of the grown substrate is a substantially uniform depth in all concave portions (in other words, a substantially uniform height in all convex portions). On the other hand, FIGS. 2a and 2b are examples of the case of the prior application, and are schematic diagrams in which fiber a, in which fine particles 2' are dispersed and contained in a fiber polymer matrix, is irradiated with plasma. In this case, since the fine particles are dispersed in the polymer matrix, the fine particles are located at uneven heights in the polymer matrix. Therefore, if such a fiber is irradiated with plasma, the depth D from the position of the fine particles that appear on the fiber surface due to plasma irradiation to the substrate surface where the fine particles are removed and is etched to form a recess will be uneven. It is.
In addition, since the positions of the fine particles are irregular and the polymer matrix located on the surface layer from the fine particles is etched and scattered by plasma irradiation, compared to the case of the present invention, when compared with the same plasma irradiation time, the average The depth of the concave portion (expressed conversely, the height of the convex portion) becomes smaller. In other words, the unevenness formed has a uniform depth (height) and the depth (height) has a more sufficient depth (height), so it satisfies friction durability, texture, and color development. It is thought that this can be obtained. The object of the present invention is not limited to synthetic fibers as described above, but also includes natural fibers such as wool, cotton, linen, and silk, semi-synthetic fibers such as acetate, and recycled fibers such as rayon. Synthetic fibers include polyester-based, polyamide-based, acrylic-based, polyurethane-based, and other synthetic fibers, but synthetic fibers include those that are partially copolymerized, blends of two components, and those that are bonded together. But that's fine. It may also contain surfactants, matting agents, pigments, and the like. The fiber structure of the present invention includes those composed of the above-mentioned fibers alone or a composite/mixture of two or more types of fibers, and is not limited to thread products such as tows, filaments, and yarns. Naturally, it may be a knitted fabric or a woven fabric made by knitting or weaving the yarn, or it may be a nonwoven fabric, and is meant to include all forms of cloth-like two-dimensional objects. Convexities made of fine particles existing on the surface of the fiber matrix are observed and measured using photographs taken with a scanning electron microscope magnifying the fiber surface more than 10,000 times. I found it to be very effective. Here, this unevenness means that the distance between the center (or near the center) of a convex part and the center (or near the center) of the next convex part is changed about 30 locations along the fiber axis direction in the above electron micrograph. This is the measured and averaged value. If this value is smaller than 0.01 micron, there will be little deep coloring effect on the dyed product, and conversely, if it is larger than 1 micron, there will be no darkening effect. Therefore, the unevenness is
A range of 0.01 to 1 micron is preferred, and 0.1
~0.5 micron is more preferred. Furthermore, it is preferable that the number of these unevenness is 1 to 200 per 1 square micron. This number was also measured by taking a photograph of the fiber surface magnified 10,000 times or more using a scanning electron microscope, and counting the number of protrusions present within a square with sides of 1 micron. When this number is 200 or more, the shape of the unevenness becomes too small and the color deepening effect is small.
Preferably it is 3 to 100 pieces. As for the manufacturing method, the present invention involves first attaching fine particles onto the fiber surface of a fiber structure, and then subjecting the fiber structure to which the fine particles are attached to a low-temperature plasma treatment before or after dyeing. can get. It is important that the fine particles in the present invention are more inert than the polymer substrate in low-temperature plasma, and include silicon-containing inorganic particles, inorganic fine particles made of oxides of metals from Group Group of the periodic table, and/or salts thereof; Fine particles selected from the group consisting of aluminum oxide, thorium oxide, and zirconium oxide and having an average primary particle diameter of less than 0.5 micron are used, more preferably 0.2 micron or less, and still more preferably 0.07 micron or less.
Below 0.07 microns and above 0.03 microns, the dyed material irradiated with low-temperature plasma tends to take on a slightly bluish tinge, while below 0.03 microns it tends to take on a slightly reddish tinge. Furthermore, it is thought that the concave portions are caused by fine particles remaining without being blown away by the plasma irradiation, as described above, and the polymer matrix taking a granular form with the remaining fine particles as cores, thus forming the convex portions. The type of fine particles used also affects the darkening effect,
Among the above-mentioned fine particles, those having a low refractive index are preferable, and in this respect, silica is most preferable. Due to its dispersibility, fine particles that are dispersed in colloidal form are best used.
It is not limited to this. A commonly used resin processing method can be used to apply the fine particles to the fiber surface.
For example, a resin liquid is applied to a fiber structure by a method such as padding, spraying, or printing, and then adjusted to an appropriate adhesion amount using a mangle or the like, and then applied to the fiber surface by dry heat or wet heat treatment. If it is desired to strengthen the adhesion between the fine particles and the fibers, the adhesive resin can be applied at the same time as the fine particles are attached, or after the fine particles are attached. As this adhesive resin, a water-dispersed emulsion is easily used, and when the adhesive resin is attached at the same time as the fine particles, it may be a combination that does not coagulate with the colloidal material of the fine particles when mixed. For example, when colloidal silica is used as the fine particles, anionic or nonionic resin emulsions are preferred since cationic resin emulsions tend to aggregate with colloidal silica. Of course, a finishing agent such as an antistatic agent may be included in the mixed system of the fine particles and the adhesive resin, and if the adhesive resin is applied after the fine particles are attached, these finishing agents may be contained in either. . However, if more adhesive resin is applied than necessary for the amount of fine particles,
Since the excellent squeaky feeling of the present invention is likely to be impaired, the ratio of the amount of adhesive resin to the amount of fine particles is 1.
It is desirable to make it smaller. Furthermore, as a method for imparting adhesion to the fibers of fine particles, it is also effective to apply plasma irradiation after the fine particles are attached, and then apply an adhesive resin. One of these methods is to attach an adhesive resin by plasma polymerization. This method has the advantage that it is possible to significantly improve durability, and at the same time, the process can be a dry process of low-temperature plasma irradiation and plasma polymerization. There are two methods for forming a resin by plasma polymerization: a method in which monomers are introduced with radicals remaining after plasma etching, and a method in which monomers are introduced under discharge conditions after plasma etching and then plasma polymerized. The adhesive resin that can be plasma-polymerized is preferably one that has a relatively low boiling point and is volatile at room temperature. Examples of such substances include acrylic acid, methacrylic acid, or esters thereof, silicon compounds, and fluorine compounds. As mentioned before, the mechanism of unevenness formation in the present invention is that the surface portion of the polymer substrate that is not shielded by fine particles is scattered by plasma irradiation and forms concave portions, but the fine particles attached to the substrate surface are not shielded by plasma irradiation. It is thought that the protrusions with the fine particles as the core are formed by remaining on the surface of the substrate without scattering even when the particles are scattered, and by leaving a portion of the substrate shielded by the fine particles. That is, it is thought that the fine particles deposited on the surface of the substrate act as a shield for the substrate, and the portions without the shield are sequentially etched into the interior of the substrate by the plasma. Therefore, based on the above idea, on the fiber surface,
In order to form many irregularities of a limited size, it is considered to be extremely important to have as many fine particles as possible as uniformly as possible on the surface of the fiber matrix. However, at the same time, if the layer of fine particles serving as a shield is thicker than necessary, etching into the interior of the substrate will be inhibited and the texture will be impaired, so it is preferable that the layer be as thin as possible. In this respect, the amount of fine particles attached to the fiber surface is preferably 0.01 to 10% by weight, more preferably 0.05 to 2% by weight, based on the fiber. The amount of adhesion
If it is less than 0.01%, the effect of improving color development and texture will be small, and if it exceeds 10%, the texture will be significantly impaired. Plasma is a state in which high energy is given to a substance, causing its molecules or atoms to dissociate and become a gas containing positive ions and an approximately equal number of anions or electrons in addition to neutral atoms. To tell. Usually, low-temperature plasma is generated by applying high voltage by low frequency, high frequency, or microwave to a gas atmosphere under reduced pressure of 10 Torr or less. The generated excited atoms, ions, electrons, etc. act on the surface of the polymer substrate, etching the surface. As the gas for generating low-temperature plasma, for example, oxygen, air, nitrogen, argon, olefin, etc. are preferably used. The conditions for low-temperature plasma treatment include equipment type, shape, gas type, flow rate, degree of vacuum, output, and treatment time, etc., which are selected appropriately depending on the material, composition, shape, and desired degree of darkening of the target fibers. There is a need to. For example, in the article obtained by the present invention, it is not necessarily necessary that the entire front and back surfaces of the fiber structure be textured, and in some cases, only one surface may be textured. Therefore, in that case, it is only necessary to make the fiber surface exposed on one side uneven, and this is done by appropriately selecting plasma treatment conditions. Regarding air, oxygen, and argon as gases used to generate low-temperature plasma, in terms of color deepening effect, the order is oxygen > air > argon, and the type of gas used also affects the effect. I understand. Furthermore, when the gas flow rate was varied while keeping the degree of vacuum constant, it was found that the etching rate had a large effect on the gas flow rate. In addition, the plasma treatment itself may be performed either before or after dyeing the fibers, but methods that are performed before dyeing may deform the unevenness formed on the fiber surface during the subsequent dyeing process, so this is a disadvantage. It is preferable to carry out this after dyeing without fear. In addition, the present invention provides a method of coating a part of the irradiated surface of the fiber structure with a coating other than the adhered fine particles, creating a part to be irradiated with plasma and a part not to be irradiated with plasma, and performing low-temperature plasma irradiation. The pattern and color of the covered part can be changed to the pattern and color of the uncovered part. In this method, the boundary between the covered part and the non-covered part is very clear,
It can give unique effects to dyed materials. Further, in the present invention, as the fibrous structure to which the fine particles are attached, a structure made of fibers whose fibers have been roughened in advance can be used. This fiber structure made of pre-roughened fibers can be produced, for example, by etching the polyester fiber pre-contained with fine particles shown above as the first known example using an alkaline solution to form specific irregularities on the fiber surface. Structures made of polyester fibers made of polyester fibers, or fiber structures made of synthetic fibers prepared by plasma etching synthetic fibers pre-contained with fine particles as shown in the example of the prior application mentioned above to form specific irregularities on the fiber surfaces. are mentioned as typical examples, but the structure is not limited to these roughened fiber structures. Among synthetic fibers, polyester fibers are the worst in the depth and clarity of dyed colors, but as described above, the technology of the present invention has a remarkable effect of improving the degree of color deepening on polyester fibers, and It can be said that this is a technique that is particularly effective for fibers. In this case, the polyester-based polymer is defined as having at least about 75% of its repeating structural units.
【式】(但し−G−は2
〜18炭素原子を含み飽和炭素原子により隣の酸素
原子と結びついている2価の有機基)の単位であ
る如きグリコールジカルボキシレート繰返し構造
単位を意味するものである。テレフタレート基は
繰返し構造単位の唯一のジカルボキシレート成分
であつてもよく、または繰返し構造単位の約25%
まではアジペート、セバケート、イソフタレー
ト、ビベンゾエート、ヘキサヒドロテレフタレー
ト、ジフエノキシエタン−4,4′−ジカルボキシ
レート、5−スルホイソフタレート基の如き他の
ジカルボキシレートを含んでいてもよい。グリコ
ール類としては、エチレングリコール、テトラメ
チレングリコール、ヘキサメチレングリコール、
等のポリメチレングリコール、2,2−ジメチル
−1,3−プロパンジオールの如き枝鎖グリコー
ル、ジエチレングリコール、トリエチレングリコ
ール、テトラエチレングリコール、あるいはこれ
らの混合物も使用できる。要すれば約15重量%ま
での高分子量ポリエチレングリコールの如き高級
グリコールも添加使用できる。
艶消剤、光沢改良剤、変色防止剤等の色々の他
の物質も要すれば重合混合物に加えてもよい。
これまでの説明で理解されるように本発明は繊
維表面を特異な構造とすることにより所期の目的
を達せんとするものであり、本発明は、天然繊
維、再生繊維、半合成繊維および合成繊維の1種
以上を混合使用してなる繊維構造物に適用される
ことは無論のこと、繊維自体が芯鞘構造や背腹構
造の複合繊維からなる繊維構造物に適用されるこ
とも無論である。
またさらに本発明は仮撚捲縮加工等の高次加工
により、五角、六角に類似した形状になつたり、
紡糸時の異形断面ノズルにより三葉形、T形、4
葉形、5葉形、6葉形、7葉形、8葉形等多葉形
や各種の断面形状として用いても良いことはいう
までもない。
本発明による仮撚加工糸ではキラキラ光るグリ
ツターも減少する効果を発揮する。このため高速
紡糸して得られるPOYのDTY仮撚糸にもアンチ
グリツター効果を発揮する意味でメリツトとな
る。
次に実施例をもつて本発明を説明するが、本発
明は以下の実施例に限定されるものではない。
当業者にとつては常識的なことではあるが、ポ
リエステル繊維からなる構造物は、該構造物のつ
や消しを行なうために繊維中に二酸化チタンを含
有させると共に、該構造物の風合を改良するため
にアルカリ溶液による減量処理加工を行なうこと
が常奪手段となつている。本発明での以下の実施
例、比較例でも、対象となる繊維素材がポリエス
テル繊維の場合には、上記のように通常使用され
るセミダル繊維使用、減量処理加工した構造物を
対象として、本発明を適用した場合の実施例につ
いて主として開示してあるが、本発明は必ずし
も、このような繊維構造物を対象として用いるこ
とが必須のことでないことは自明である。
Aシリーズ実施例及び比較例
平均一次粒子径200ミリミクロンの二酸化チタ
ン0.45重量%を添加した固有粘度〔η〕0.69のポ
リエチレンテレフタレートポリマー(これは前記
のいわゆるセミダルポリエステル繊維をつくる場
合のTiO2含有ポリエステルポリマーである)と、
二酸化チタンなどの微粒子を全く混入しない固有
粘度〔η〕0.69のポリエチレンテレフタレートポ
リマーを通常の製造方法によつて製造し、それぞ
れのポリマーを用い、通常の方法で紡糸・延伸
し、75デニール/36フイラメントの断面円形の繊
維をそれぞれ得た。次にこのそれぞれのフイラメ
ントを合糸し150デニールとして2100回/米でS
撚とZ撚の実撚を行ない、熱セツト後、タテ糸、
ヨコ糸に用いてチリメンジヨーゼツト織物をつく
つた。この織物をシボ立て後熱セツトし、シリカ
とポリエステルとの共通溶媒である水酸化ナトリ
ウム水溶液40g/、98℃にて、それぞれ減量率
25%となるように減量した。その後染料として、
日本化薬社製のKayalon Polvester Black G−
SFを12%o.w.fで、分散剤として東邦化学社製の
界面活性剤Tohosalt TD0.5g/、PH調整剤に
大和化学工業製のUltra Mt−N2(酢酸と酢酸ソ
ーダの混合液)0.7g/を加えて135℃に染色
し、ハイドロサルフアイト1g/、苛性ソーダ
1g/、ノニオン活性剤1g/にて80℃、10
分間還元・洗浄を行なつて黒染品とした。
これらの黒染めされた織物に、平均一次粒径45
ミリミクロン(mμ)のコロイダルシリカを付着
させ、その付着量、ならびに接着性樹脂の有無を
変化させて、種々の、シリカ付着織物をつくつ
た。コロイダルシリカの付着はパツドードライ法
で行なつた。
得られた各種織物を内部電極型のプラズマ装置
内(電極面積50cm2)に入れ、周波数13.56MHz、
導入ガスとして酸素、空気を用い、真空度0.05〜
1Torr、出力50ワツトで1〜5分間のプラズマ照
射をした。得られたものの濃色度は日立製作所製
の自記分光光度計を用いて測定した。染色物の濃
色度はL*a*b*の係表示のL*値で示してあり、小
さいほど濃色効果が大きいことを示す。
第1表のA−1、A−3から理解されるよう
に、繊維表面へ微粒子を付着させないでプラズマ
照射したもののL*の低下は小さく、濃色効果は
少ない。またこの場合の繊維表面を走査型電子顕
微鏡で観察すると繊維軸方向に直交する方向に長
いうね状の凹凸形態が形成されていた。
A−2、A−4〜A−15の場合のようにシリカ
ゾルを繊維表面に付着させてプラズマ照射した場
合は、著るしくL*値の低下があり濃色効果が上
がることが理解される。そしてこれ等の場合の繊
維表面を、上記と同じく走査型電子顕微鏡で観察
すると、凸部中心間距離が0.01〜1μで、一平方ミ
クロン(1μ2)あたり1〜200個の凸部構造があ
り、方向性のない凹凸構造が形成されていた。A
−4〜A−6、A−13〜A−15からシリカの付着
量において0.01重量%のときでも既に充分な効果
が発現されることが理解され、またより好適な範
囲が存在することもわかる。またA−6〜A−8
において照射時間が長くなるとL*値の低下も著
るしく濃色効果が高くなることがわかる。特にA
−8のものは得られた織物はベルベツトの如き発
色性を示した。A−9、A−10は接着性樹脂を付
着させた例で、いずれも濃色効果は上つており、
接着性樹脂を付着させない例えばA−6に比べて
耐洗濯耐久性が向上しているが、A−10の場合は
接着性樹脂量がやや多いため、得られた織物はヌ
メリ感がでて好ましいものではなかつた。A−
11、A−12は接着性樹脂を付着させる他の例で、
この場合も濃色効果があり、耐洗濯性が向上して
いる。[Formula] (where -G- is a divalent organic group containing 2 to 18 carbon atoms and connected to the adjacent oxygen atom through a saturated carbon atom) is a glycol dicarboxylate repeating structural unit such as It is. The terephthalate group may be the only dicarboxylate component of the repeating structural unit, or about 25% of the repeating structural unit.
It may also contain other dicarboxylates such as adipate, sebacate, isophthalate, bibenzoate, hexahydroterephthalate, diphenoxyethane-4,4'-dicarboxylate, 5-sulfoisophthalate groups. Glycols include ethylene glycol, tetramethylene glycol, hexamethylene glycol,
Polymethylene glycols such as, branched chain glycols such as 2,2-dimethyl-1,3-propanediol, diethylene glycol, triethylene glycol, tetraethylene glycol, or mixtures thereof can also be used. If desired, up to about 15% by weight of higher glycols such as high molecular weight polyethylene glycols can also be used. Various other substances such as matting agents, gloss improvers, anti-tarnish agents, etc. may also be added to the polymerization mixture if desired. As understood from the above explanation, the present invention aims to achieve the intended purpose by giving the fiber surface a unique structure. It goes without saying that it can be applied to fiber structures made of a mixture of one or more types of synthetic fibers, as well as fiber structures made of composite fibers in which the fiber itself has a core-sheath structure or a dorsal-ventral structure. It is. Furthermore, the present invention can be made into a shape similar to a pentagon or hexagon by high-order processing such as false twisting and crimp processing,
Trilobal, T-shaped, and 4-shaped fibers are produced by the irregular cross-section nozzle during spinning.
Needless to say, it may be used in a multi-lobed shape such as a leaf shape, a five-lobed shape, a six-lobed shape, a seven-lobed shape, an eight-lobed shape, etc., and various cross-sectional shapes. The false twisted yarn according to the present invention exhibits the effect of reducing glitter. Therefore, it is advantageous in that it also exhibits an anti-glitter effect on the POY DTY false twisted yarn obtained by high-speed spinning. Next, the present invention will be explained with reference to examples, but the present invention is not limited to the following examples. As is common knowledge to those skilled in the art, structures made of polyester fibers contain titanium dioxide in the fibers to make the structure matte and to improve the texture of the structure. For this reason, it has become a common practice to carry out weight reduction processing using an alkaline solution. In the following Examples and Comparative Examples of the present invention, when the target fiber material is polyester fiber, the present invention is applied to a structure using normally used semidal fibers and subjected to weight reduction treatment as described above. Although the embodiments are mainly disclosed in which the present invention is applied, it is obvious that the present invention does not necessarily have to be applied to such a fiber structure. A series examples and comparative examples A polyethylene terephthalate polymer with an intrinsic viscosity [η] of 0.69 to which 0.45% by weight of titanium dioxide with an average primary particle diameter of 200 millimicrons is added (this is the TiO 2- containing polymer used to make the so-called semi-dull polyester fiber mentioned above). polyester polymer) and
A polyethylene terephthalate polymer with an intrinsic viscosity [η] of 0.69 containing no particulates such as titanium dioxide was produced using a normal manufacturing method, and each polymer was spun and drawn using a normal method to form a 75 denier/36 filament. Each fiber with a circular cross section was obtained. Next, these filaments were combined into 150 denier threads for 2100 times/S.
Perform actual twisting of twisting and Z twisting, and after heat setting, warp yarn,
It was used as a weft to create chilimenji yosetsu fabric. This fabric was embossed and heat set, and the weight loss rate was 40g/40g/aqueous sodium hydroxide solution, which is a common solvent for silica and polyester, at 98°C.
The weight was reduced to 25%. Later, as a dye,
Kayalon Polvester Black G- manufactured by Nippon Kayaku Co., Ltd.
SF at 12% owf, surfactant Tohosalt TD manufactured by Toho Chemical Co., Ltd. as a dispersant, 0.5 g/, and Ultra Mt-N 2 (mixture of acetic acid and sodium acetate) manufactured by Daiwa Chemical Industry Co., Ltd. as a PH adjuster, 0.7 g/ was added and dyed at 135°C, and dyed at 80°C for 10 minutes with 1 g of hydrosulfite, 1 g of caustic soda, and 1 g of nonionic activator.
The product was reduced and washed for several minutes to obtain a black dyed product. These black-dyed fabrics have an average primary particle size of 45
Millimicron (mμ) colloidal silica was deposited, and various silica-deposited fabrics were created by varying the amount of colloidal silica deposited and the presence or absence of adhesive resin. Colloidal silica was attached using the Patsudo dry method. The various fabrics obtained were placed in an internal electrode type plasma device (electrode area 50 cm 2 ), and the frequency was 13.56 MHz.
Using oxygen and air as introduced gas, vacuum degree 0.05~
Plasma irradiation was performed for 1 to 5 minutes at 1Torr and 50W output. The color density of the obtained product was measured using a self-recording spectrophotometer manufactured by Hitachi, Ltd. The depth of color of a dyed product is indicated by the L * value of L * a * b * , and the smaller the value, the greater the darkening effect. As can be seen from A-1 and A-3 in Table 1, when plasma irradiation was performed without fine particles being attached to the fiber surface, the decrease in L * was small and the darkening effect was small. Furthermore, when the fiber surface in this case was observed using a scanning electron microscope, it was found that long ridge-like irregularities were formed in a direction perpendicular to the fiber axis direction. It is understood that when silica sol is attached to the fiber surface and plasma irradiated as in the case of A-2, A-4 to A-15, the L * value decreases significantly and the darkening effect increases. . When the fiber surface in these cases is observed using a scanning electron microscope as described above, the distance between the centers of the protrusions is 0.01 to 1μ, and there are 1 to 200 protrusions per square micron (1μ 2 ). , an uneven structure with no directionality was formed. A
From -4 to A-6 and A-13 to A-15, it is understood that a sufficient effect is already expressed even when the amount of silica attached is 0.01% by weight, and it is also understood that a more suitable range exists. . Also A-6 to A-8
It can be seen that as the irradiation time increases, the L * value decreases significantly and the darkening effect increases. Especially A
-8, the resulting fabric exhibited velvet-like color development. A-9 and A-10 are examples with adhesive resin attached, and the dark color effect has improved in both cases.
Washing resistance is improved compared to, for example, A-6, which does not have adhesive resin attached, but A-10 has a slightly higher amount of adhesive resin, so the resulting fabric has a slimy feel, which is preferable. It wasn't something. A-
11, A-12 is another example of attaching adhesive resin,
In this case as well, there is a deep color effect and the washing resistance is improved.
【表】【table】
【表】
Bシリーズ実施例
市販のウール織物、レーヨン織物およびポリエ
ステルとトリアセテートとの混紡織物の黒染め品
にそれぞれパツド−ドライ法で0.5重量%付着さ
せてプラズマ照射した。第2表のB−1〜B−3
で示されるように、それぞれの織物はさらに濃色
効果が上がることがわかる。またこの場合の各繊
維表面をそれぞれ走査型電子顕微鏡で観察した
が、凸部中心部間距離が0.01〜1μで一平方ミクロ
ンあたり1〜200個の凸部構造がある凹凸構造が
形成されていた。[Table] B Series Examples Commercially available wool fabrics, rayon fabrics, and black-dyed products of blended fabrics of polyester and triacetate were each coated with 0.5% by weight by pad-dry method and plasma irradiated. B-1 to B-3 in Table 2
As shown in , it can be seen that each fabric has an even deeper color effect. In addition, the surface of each fiber in this case was observed using a scanning electron microscope, and it was found that a concavo-convex structure was formed with a distance between the centers of convexities of 0.01 to 1μ and 1 to 200 convexities per square micron. .
【表】【table】
【表】
Cシリーズ実施例及び比較例
AシリーズA−3〜A−14で用いたポリエチレ
ンテレフタレートポリマーと、シリカを添加した
固有粘度〔η〕0.69の各ポリエチレンテレフタレ
ートポリマーとを用意した。尚シリカ添加ポリマ
ーは、平均一次粒子径45ミリミクロン、濃度20重
量%の水系シリカゾルを室温でエチレングリコー
ルに混合し、充分撹拌した後テレフタル酸と混合
し、次いで直接重合を行なつてシリカ含有ポリマ
ーを得る方法で、水系シリカゾルの添加量をそれ
ぞれかえ、第3表の如きシリカ添加量の異なる固
有粘度〔η〕0.69のポリエチレンテレフタレート
ポリマーを得た。これら用意したポリマーを用
い、以後はAシリーズと同じ条件で、繊維をつく
り、該繊維からチリメンジヨーゼツト織物をつく
り、減量処理し、染色した。
この黒染めされた織物に付着させる微粒子の粒
径、付着させる微粒子の種類の影響およびポリマ
ー中へ添加する微粒子を増加させた場合について
の結果が第3表で示される。C−1〜C−4で
は、付着させる微粒子の平均粒径が細かい程L*
の低下が大きく、濃色効果の向上が高いことがわ
かる。なお微粒子の粒径が15mμのC−1場合は
やや赤味のある黒色となり、粒径が45mμのC−
2の場合はやや青味のある黒色となつた。付着さ
せる微粒子の種類としては比較的屈折率の低いシ
リカが好ましいことが示される。
C−9〜C−14によつて、シリカをポリマー中
に混入して繊維をつくり、この繊維をアルカリに
より減量処理すれば、それだけで既に濃色効果が
認められ特にシリカ添加量が増加してくるとアル
カリ処理よる繊維表面の粗面化がより発現し、そ
れによる濃色効果がはつきりと向上することが示
される。そしてこれら予め粗面化された黒染め品
にさらに微細子を被覆し、プラズマ照射すること
によつて、さらに当初の粗面化程度に対応して濃
色化効果が向上することが示される。
またC−15は微細子を被覆させずにプラズマ照
射した場合の例で、本文中の前記説明の先願に相
当する例である。この場合は、繊維中に3%の微
粒子を混入してアルカリ減量加工されたもので、
それ自体ですでにある程度濃色効果の優れたもの
であるが、この物にプラズマ照射したときのL*
値の低下は、表面に微粒子を付着させた点のみ異
なるC−12の場合と比べて、小さい。[Table] C Series Examples and Comparative Examples The polyethylene terephthalate polymers used in A series A-3 to A-14 and each polyethylene terephthalate polymer containing silica and having an intrinsic viscosity [η] of 0.69 were prepared. The silica-added polymer is prepared by mixing an aqueous silica sol with an average primary particle size of 45 millimicrons and a concentration of 20% by weight in ethylene glycol at room temperature, stirring thoroughly, mixing with terephthalic acid, and directly polymerizing it to obtain a silica-containing polymer. By varying the amount of aqueous silica sol added, polyethylene terephthalate polymers with different intrinsic viscosities [η] of 0.69 and different amounts of silica were obtained as shown in Table 3. Using these prepared polymers, fibers were made under the same conditions as in the A series, and a chillimendiyosette fabric was made from the fibers, subjected to weight reduction treatment, and dyed. Table 3 shows the effects of the particle size of the fine particles attached to this black-dyed fabric, the type of fine particles attached, and the results when the amount of fine particles added to the polymer was increased. For C-1 to C-4, the finer the average particle diameter of the particles to be attached, the smaller the L *
It can be seen that the decrease in color is large, and the darkening effect is greatly improved. In addition, in the case of C-1 with a particle size of 15 mμ, the color is slightly reddish black, and in the case of C-1 with a particle size of 45 mμ.
In the case of 2, the color was black with a slight bluish tinge. It is shown that silica, which has a relatively low refractive index, is preferable as the type of fine particles to be deposited. By mixing silica into polymers using C-9 to C-14 to make fibers, and then reducing the fibers with alkali, a deep coloring effect can already be observed, especially when the amount of silica added increases. It is shown that the roughening of the fiber surface due to the alkali treatment becomes more apparent, and the resulting deep coloring effect is significantly improved. Furthermore, it has been shown that by further coating these black-dyed products whose surfaces have been roughened in advance with fine particles and irradiating them with plasma, the color deepening effect is further improved in accordance with the initial degree of surface roughening. Further, C-15 is an example in which plasma irradiation was performed without coating microparticles, and is an example corresponding to the earlier application described above in the main text. In this case, the fiber has been subjected to alkali reduction treatment by mixing 3% of fine particles into the fiber.
It already has a good deep color effect to some extent, but when this object is irradiated with plasma, the L *
The decrease in value is smaller than in the case of C-12, which differs only in that fine particles are attached to the surface.
【表】【table】
【表】
Dシリーズ実施例および比較例
このシリーズの例は、本発明が黒色以外のいか
なる色の染色物および2種以上の色が組合わされ
た染色物についても適用できることを示す例であ
り、その構成および効果が第4表に示される。前
記L*値は、黒色における明度の示標であつて、
明度がより低いことが、黒色がより黒いことであ
るが、黒以外の色にあつては彩度が高いことが、
その色の鮮明度を示すものであつて、その色の彩
度についてはL*値の如き信頼性のある数値化が
できず、本明細書ではこの色の鮮明度について
は、以下のように肉眼判定して評価している。ま
たきしみ感についても手ざわりでの評価である。[Table] D Series Examples and Comparative Examples This series of examples shows that the present invention can be applied to dyed products of any color other than black and to dyed products that are a combination of two or more colors. The configuration and effects are shown in Table 4. The L * value is an indicator of the lightness of black,
Lower brightness means black is darker, but for colors other than black, higher saturation means black is darker.
It indicates the vividness of the color, and the saturation of the color cannot be quantified as reliable as the L * value, so in this specification, the vividness of the color is expressed as follows. Evaluation is done by visual judgment. The squeakiness was also evaluated based on the feel.
【表】
Aシリーズ実施例で製造した場合と全く同様に
して、通常の製造方法によりポリエチレンテレフ
タレートポリマーをつくりこのポリマーからさら
に通常の製造方法により、それぞれ50デニール
(dr)/36フイラメント(f)および75dr/36fの延伸
糸を作成した。この延伸糸を用い通常の製造方
法、規格にしたがつて、平羽二重、綾羽二重、パ
レス、ヨウリユウおよびシホンを作成し、それぞ
れアルカリによる減量加工を行なつた。以上で得
られたそれぞれの構造物を出発構造物とした。
第4表のD−1〜D−4では、プラズマ照射の
みでは本発明の効果なく、微粒子付着のみでも効
果少なく、微粒子を付着させてプラズマ照射し
て、はじめて優れた効果が得られることが示され
る。特にD−4で得られた平羽二重は、光沢があ
りしかも色が鮮やかとなり、D−1〜D−3と比
べて著るしい差があつた。またきしみ感について
も著しく優れ絹以上の独特のきしみ感とふくらみ
感を有していた。D−5は、前記C−12、C−15
と同じポリマーを用いて前記延伸糸とし、平羽二
重をつくり、アルカリによる減量処理を行なつた
例であるが、この減量処理のみで得られた平羽二
重の色は濃色ではあるが光沢がないものであつ
た。
D−6は付着微粒子を変性ポリビニルアルコー
ルで接着強化した例であるが、D−4以上に洗濯
に対して光沢、色、風合の耐久性を有していた。
D−7〜D−10は綾羽二重の例で、D−8〜D
−10はD−7に比較して光沢及び色の鮮明性が著
るしく優れていると同時にきしみ感が大で絹以上
の風合となつた。またメチルトリメトキシシラン
及びC2F4ガスをプラズマ重合させたD−9、D
−10はD−8に比較して優れた洗濯耐久性を示
し、洗濯50回で光沢、色、風合はまつたく変化し
なかつた。
D−11〜D−14がパレス、ヨウリユウ、シホン
の例で、D−12〜D−14の本発明品はポリエステ
ルとは思えない程光沢のある鮮やかな色ときしみ
感を有していた。[Table] A polyethylene terephthalate polymer was prepared using a conventional manufacturing method in exactly the same manner as in the A series examples, and a 50 denier (dr)/36 filament (f) and a 50 denier (dr)/36 filament (f) and A drawn yarn of 75 dr/36 f was prepared. Using this drawn yarn, flat feather doubles, twill feather doubles, palaces, lily pads, and chiffons were prepared according to conventional manufacturing methods and specifications, and weight reduction processing using an alkali was performed on each yarn. Each of the structures obtained above was used as a starting structure. D-1 to D-4 in Table 4 show that plasma irradiation alone does not have the effect of the present invention, that fine particle attachment alone has little effect, and excellent effects can only be obtained by plasma irradiation with fine particles attached. It will be done. In particular, the flat feather doublet obtained in D-4 was glossy and bright in color, and there was a significant difference compared to D-1 to D-3. It was also extremely superior in terms of squeaky feel, with a unique squeaky and fluffy feel that was better than that of silk. D-5 is the above C-12, C-15
In this example, the same polymer as above was used as the drawn yarn to make a flat feather doublet, and a weight loss treatment with an alkali was performed. was lackluster. D-6 is an example in which adhesion of adhered fine particles was strengthened with modified polyvinyl alcohol, and it had better durability against washing in terms of gloss, color, and texture than D-4. D-7 to D-10 are examples of Aya Habutae, and D-8 to D
-10 was significantly superior in gloss and color clarity compared to D-7, and at the same time had a more squeaky feel and a texture better than silk. In addition, D-9 and D were produced by plasma polymerization of methyltrimethoxysilane and C 2 F 4 gas.
-10 showed superior washing durability compared to D-8, and the gloss, color, and texture did not change appreciably after 50 washes. D-11 to D-14 are examples of palace, porcelain, and chiffon, and the products of the present invention, D-12 to D-14, had such bright colors and a squeaky feel that it was hard to believe that they were made of polyester.
【表】【table】
【表】
Eシリーズ実施例および比較例
このシリーズの例は構造物の種類、あるいは構
造物を構成する繊維素材の種類を変えた場合の例
で、その構成および効果は第5表に示される。
E−1〜E−4のポリマーはAシリーズで用い
たポリマーであり、これを常法より紡糸し、
100dr/48fの延伸糸を作成し、仮撚加工をおこな
い、さらに常法にしたがつてカシドス織物あるい
はトロマツト織物を作成した。E−1〜E−4に
おいて、微粒子を繊維表面に付着させてプラズマ
照射したE−2、E−4は微粒子を付着させない
でプラズマ照射したE−1、E−3に比しL*値
の低下が大きく、グリツターの程度も減少し、黒
の濃色度合もウール織物以上のすばらしいものと
なつた。
E−5〜E−8は繊維素材としてポリブチレン
テレフタレート繊維あるいはナイロン繊維を用い
るもので、各々の40dr/24fの延伸糸を使用し、
トリコートの編地に作成した例である。この例で
も、E−6あるいはE−8は、各々E−5あるい
はE−7に比し、光沢のある鮮明な色となり高級
感が一層増した。
E−9〜E−10は繊維素材としてスルホイソフ
タル酸を2.5モル%共重合させたポリエチレンテ
レフタレート繊維を用いるもので、その50dr/
36fの延伸糸から常法にしたがつて朱子織物に作
成した例である。この例でも、E−10はE−9に
比し、朱子織物独特の光沢を保持した鮮明な色と
なり、風合もきしみ感が現われ、溶融紡糸繊維独
特のワキシー感も消失して絹の如き風合となつ
た。
E−11〜E−13は、E−1〜E−4のポリマー
と同じポリエチレンテレフタレートポリマーから
75dr/36fの延伸糸をつくり、加撚加工し、常法
によつてクレポンジヨオゼツトとした例である。
微粒子を繊維表面に付着させてプラズマ照射した
E−12、E−13の場合は微粒子を付着させないで
プラズマ照射したE−11の場合に比し、いずれも
著るしい濃色黒となり、レーヨンジヨオゼツト、
ウールジヨオゼツト、あるいはトリアセテート/
ポリエステル混ジヨオゼツトより濃色となつた。
またシランカツプリング材を接着性樹脂として用
いたE−13の場合はE−12の場合に比し洗濯耐久
性も向上した。
また走査型電子顕微鏡での繊維表面についての
観察によれば、各比較例は繊維軸方向に直交する
方向に向いた長いうね状の凹凸形態が形成されて
いるのに対し、各実施例のものは、繊維表面に微
細な方向性のない凹凸が形成され、その凸部中心
間距離が0.01〜1μで、1平方ミクロンあたり1〜
200個の凸部が存在するものであつた。[Table] E Series Examples and Comparative Examples The examples in this series are examples in which the type of structure or the type of fiber material constituting the structure is changed, and the structure and effects are shown in Table 5. Polymers E-1 to E-4 are the polymers used in the A series, and are spun using a conventional method.
A drawn yarn of 100 dr/48 f was prepared, subjected to false twisting, and then a Kasidos fabric or Tolomatsu fabric was fabricated according to a conventional method. Among E-1 to E-4, E-2 and E-4, which were subjected to plasma irradiation with fine particles attached to the fiber surface, had a lower L * value compared to E-1 and E-3, which were subjected to plasma irradiation without fine particles attached. The reduction was large, the degree of glitter was also reduced, and the degree of black darkness was even greater than that of wool fabrics. E-5 to E-8 use polybutylene terephthalate fiber or nylon fiber as the fiber material, and use each drawn yarn of 40 dr/24 f.
This is an example of a tric coat knitted fabric. In this example as well, E-6 or E-8 had a brighter, glossier color than E-5 or E-7, respectively, and the sense of luxury was further enhanced. E-9 to E-10 use polyethylene terephthalate fiber copolymerized with 2.5 mol% of sulfoisophthalic acid as the fiber material, and their 50 dr/
This is an example of a satin fabric made from 36f drawn yarn using a conventional method. In this example, compared to E-9, E-10 has a brighter color that retains the unique luster of satin fabrics, has a squeaky texture, and loses the waxy feel unique to melt-spun fibers, giving it a silk-like appearance. It became a texture. E-11 to E-13 are made from the same polyethylene terephthalate polymer as E-1 to E-4.
This is an example of making a drawn yarn of 75 dr/36 f, twisting it, and making it into a crepond jersey using a conventional method.
In the case of E-12 and E-13, in which fine particles were attached to the fiber surface and irradiated with plasma, compared to the case of E-11, which was irradiated with plasma without fine particles attached, both became significantly darker black, and rayon jersey. Ozets,
Wool oyster or triacetate/
The color was darker than that of the polyester blend.
In addition, in the case of E-13, in which a silane coupling material was used as the adhesive resin, the washing durability was improved compared to the case of E-12. Furthermore, according to the observation of the fiber surface using a scanning electron microscope, each comparative example had long ridge-like unevenness oriented in a direction perpendicular to the fiber axis direction, whereas each of the examples The fiber surface has fine unevenness with no directionality, and the distance between the centers of the convexities is 0.01 to 1μ, and the density is 1 to 1μ per square micron.
There were 200 protrusions.
【表】【table】
第1図および第2図は、凹凸生成の原理を説明
した模式図である。即ち、第1図は、繊維表面
に、プラズマの遮蔽物となる微粒子を被覆付着し
ておき、その繊維にプラズマを照射する場合の模
式図、第2図は繊維基質中に微粒子を分散含有さ
せておき、その繊維にプラズマを照射する場合の
模式図である。
1……繊維表層部分、2,2′……微粒子。
FIGS. 1 and 2 are schematic diagrams illustrating the principle of generating unevenness. That is, Fig. 1 is a schematic diagram of the case where the fiber surface is coated with fine particles that serve as a plasma shield and the fiber is irradiated with plasma, and Fig. 2 is a schematic diagram of the case where the fine particles are dispersed and contained in the fiber matrix. FIG. 3 is a schematic diagram of the case where the fiber is irradiated with plasma. 1...Fiber surface layer portion, 2,2'...Fine particles.
Claims (1)
質に比しより不活性である微粒子を繊維表面に付
着させた繊維構造物にプラズマ照射してなる繊維
構造物であつて、ポリマー基質の微粒子で遮蔽さ
れない部分はプラズマでエツチングされて凹部を
形成し、微粒子で遮蔽された部分は微粒子と共に
エツチングされずに凸部を形成して繊維表面上に
凹凸を形成しており、該凹凸は互いに隣接する凸
部間の中心間距離が0.01ないし1ミクロンであ
り、該凸部が1平方ミクロン当たり1ないし200
個存在している粗面化された繊維構造物。 2 繊維表面に付着させた微粒子がその平均一次
粒子径が0.5ミクロン以下のものであり、該微粒
子が繊維重量に対して0.01ないし10重量%付着さ
れてなる特許請求の範囲第1項記載の粗面化され
た繊維構造物。 3 繊維表面に付着させた微粒子が、含ケイ素無
機微粒子、周期律表第族金属の酸化物およびま
たはその塩類からなる無機微粒子、酸化アルミニ
ウム、酸化トリウムおよび酸化ジルコニウムから
なる群から選ばれる1種または2種以上の無機微
粒子である特許請求の範囲第1項または第2項記
載の粗面化された繊維構造物。 4 微粒子と繊維とが、繊維に対して0.01ないし
10重量%の接着性物質で結合されてなる特許請求
の範囲第1項ないし第3項のいずれかに記載の粗
面化された繊維構造物。 5 低温プラズマ中で繊維を構成するポリマー基
質に比しより不活性である平均一次粒子径が0.5μ
以下の微粒子を繊維表面に繊維に対して0.01ない
し10重量%付着させる工程、該微粒子を付着させ
た繊維構造物に低温プラズマ照射を行なう工程、
を包含する繊維表面上に凹凸を形成させる粗面化
された繊維構造物の製造方法。 6 繊維表面に付着させる微粒子が、含ケイ素無
機微粒子、周期律表第族金属の酸化物およびま
たはその塩類からなる無機微粒子、酸化アルミニ
ウム、酸化トリウムおよび酸化ジルコニウムから
なる群から選ばれる1種または2種以上の無機微
粒子である特許請求の範囲第5項記載の粗面化さ
れた繊維構造物の製造方法。[Scope of Claims] 1. A fiber structure obtained by plasma irradiation of a fiber structure in which fine particles, which are more inert than the polymer matrix constituting the fiber, are attached to the fiber surface in a low-temperature plasma, The portions of the substrate that are not shielded by the fine particles are etched by plasma to form concave portions, and the portions that are shielded by the fine particles are not etched together with the fine particles and form convex portions, forming unevenness on the fiber surface. The center-to-center distance between adjacent convex portions is 0.01 to 1 micron, and the convex portion is 1 to 200 per square micron.
A roughened fibrous structure exists. 2. The coarse particles according to claim 1, wherein the fine particles attached to the fiber surface have an average primary particle size of 0.5 microns or less, and the fine particles are attached in an amount of 0.01 to 10% by weight based on the weight of the fiber. Faceted fiber structure. 3. The fine particles attached to the fiber surface are one selected from the group consisting of silicon-containing inorganic fine particles, inorganic fine particles consisting of oxides and/or salts of group metals of the periodic table, aluminum oxide, thorium oxide, and zirconium oxide, or The roughened fibrous structure according to claim 1 or 2, which comprises two or more types of inorganic fine particles. 4 Fine particles and fibers are 0.01 to
A roughened fibrous structure according to any one of claims 1 to 3, which is bonded with 10% by weight of an adhesive substance. 5 The average primary particle diameter is 0.5μ, which is more inert than the polymer matrix that makes up the fiber in low-temperature plasma.
A step of attaching the following fine particles to the fiber surface in an amount of 0.01 to 10% by weight relative to the fiber, a step of irradiating the fiber structure to which the fine particles are attached with low-temperature plasma,
A method for producing a roughened fiber structure, which comprises forming irregularities on the fiber surface. 6. The fine particles to be attached to the fiber surface are one or two selected from the group consisting of silicon-containing inorganic fine particles, inorganic fine particles consisting of oxides and/or salts of group metals of the periodic table, aluminum oxide, thorium oxide, and zirconium oxide. 6. The method for producing a roughened fibrous structure according to claim 5, wherein the inorganic fine particles are at least one species.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3330183A JPS59163471A (en) | 1983-02-28 | 1983-02-28 | Surface roughened fier structure and production thereof |
| CA000448343A CA1217625A (en) | 1983-02-28 | 1984-02-27 | Fibrous structure having roughened surface and process for producing same |
| DE8484102038T DE3483540D1 (en) | 1983-02-28 | 1984-02-27 | FIBROUS MATERIAL WITH RAUGED SURFACE AND METHOD FOR THE PRODUCTION THEREOF. |
| EP19840102038 EP0117561B1 (en) | 1983-02-28 | 1984-02-27 | Fibrous structure having roughened surface and process for producing same |
| KR1019840000987A KR860001824B1 (en) | 1983-02-28 | 1984-02-28 | Fibrous structure having rough end surface and process for producing same |
| US06/584,331 US4522873A (en) | 1983-02-28 | 1984-02-28 | Fibrous structure having roughened surface |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3330183A JPS59163471A (en) | 1983-02-28 | 1983-02-28 | Surface roughened fier structure and production thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59163471A JPS59163471A (en) | 1984-09-14 |
| JPH0242938B2 true JPH0242938B2 (en) | 1990-09-26 |
Family
ID=12382722
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3330183A Granted JPS59163471A (en) | 1983-02-28 | 1983-02-28 | Surface roughened fier structure and production thereof |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59163471A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6059171A (en) * | 1983-05-16 | 1985-04-05 | 株式会社クラレ | Surface roughened fiber structure and its production |
| JPH01148831A (en) * | 1987-12-02 | 1989-06-12 | Kuraray Co Ltd | Polyester fabric product and its production |
-
1983
- 1983-02-28 JP JP3330183A patent/JPS59163471A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59163471A (en) | 1984-09-14 |
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