JP3972280B2 - Manufacturing method of synthetic fiber products with excellent hygiene - Google Patents
Manufacturing method of synthetic fiber products with excellent hygiene Download PDFInfo
- Publication number
- JP3972280B2 JP3972280B2 JP26906399A JP26906399A JP3972280B2 JP 3972280 B2 JP3972280 B2 JP 3972280B2 JP 26906399 A JP26906399 A JP 26906399A JP 26906399 A JP26906399 A JP 26906399A JP 3972280 B2 JP3972280 B2 JP 3972280B2
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- Prior art keywords
- polyester
- fiber
- fiber product
- synthetic fiber
- producing
- 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.)
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- 239000012209 synthetic fiber Substances 0.000 title claims description 17
- 229920002994 synthetic fiber Polymers 0.000 title claims description 17
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000000835 fiber Substances 0.000 claims description 40
- 229920000728 polyester Polymers 0.000 claims description 40
- 230000000844 anti-bacterial effect Effects 0.000 claims description 34
- 150000001875 compounds Chemical class 0.000 claims description 16
- 239000003899 bactericide agent Substances 0.000 claims description 15
- 238000010023 transfer printing Methods 0.000 claims description 9
- 125000002091 cationic group Chemical group 0.000 claims description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 238000004898 kneading Methods 0.000 claims 1
- 150000002894 organic compounds Chemical class 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 30
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- 239000004744 fabric Substances 0.000 description 23
- 239000000047 product Substances 0.000 description 17
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- 238000011282 treatment Methods 0.000 description 8
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- 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 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
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- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
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- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 206010041925 Staphylococcal infections Diseases 0.000 description 2
- 241000191967 Staphylococcus aureus Species 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
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- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
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- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
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- 229920002647 polyamide Polymers 0.000 description 2
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- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 1
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- VCRZAKVGPJFABU-UHFFFAOYSA-N 10-phenoxarsinin-10-yloxyphenoxarsinine Chemical compound C12=CC=CC=C2OC2=CC=CC=C2[As]1O[As]1C2=CC=CC=C2OC2=CC=CC=C21 VCRZAKVGPJFABU-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- 239000005745 Captan Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000588747 Klebsiella pneumoniae Species 0.000 description 1
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- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
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- 229940117949 captan Drugs 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
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- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
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- IUEBEACSGQRJBB-UHFFFAOYSA-N methyl n-(1h-imidazol-2-yl)carbamate Chemical compound COC(=O)NC1=NC=CN1 IUEBEACSGQRJBB-UHFFFAOYSA-N 0.000 description 1
- 239000013586 microbial product Substances 0.000 description 1
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Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Coloring (AREA)
Description
【0001】
【発明の属する技術分野】
本発明は衛生性に優れる合成繊維製品の加工法、更に詳しくはポリエステルおよび変性ポリエステル系繊維組織内に殺菌剤を固定化して該繊維に衛生性を持たせる方法に関する。
【0002】
【従来の技術】
靴下、肌着、スポーツ衣料、寝具等は使用者の皮膚よりの分泌物、汗、皮膚の剥離物等が付着し、これらが栄養源となって細菌、ダニ等の微生物が繁殖する良好な培地となり、微生物の生産物によって不快感を発生し、場合によっては皮膚病等の感染原因ともなる。また、蒲団、敷物、カーテン、壁布地等は保管の際や湿度の高い場所で使用する場合等に黴が発生して繊維の劣化汚染等による品位の低下がおこる。
【0003】
繊維製品を細菌、ダニ等の微生物や黴から保護して衛生的に保ち、また品位を良好に維持する目的で繊維製品に殺菌剤を固着させる試みがなされ、今までに幾つかの方法が実施されている。最も一般的には殺菌剤を含む液に繊維製品を浸漬或いは噴霧する方法が、更に殺菌剤の固着を強力にする方法として、例えば、殺菌性第4級アンモニュウム塩の分子の一部を有機シリコン化合物を介して繊維分子の一部に結合する方法、或いは有機塩素化合物等の殺菌性化合物を展開性のよい合成樹脂で繊維表面に被覆接着して固定化する方法、或いは無機金属(銀系など)を繊維中に練込む方法、或いは繊維物質の組成中に有機金属化合物を結合させて抗菌性を持たせる方法などが知られている。
【0004】
しかしこれらの対象として用いられる繊維は専ら木綿、毛、絹、アセテート、アクリル系、ポリアミド系、塩化ビニール系、ポリウレタン系等である。
【0005】
これらの物質は原則として繊維構成分子中に第三物質分子と化学的または物理的に結合する性能を有する官能基を持ているか又は改質によりこのような官能基を導入したもの、或いは繊維表面の物性が合成樹脂接着剤との親和性に優れたものである。
【0006】
また、一般に繊維との親和性が高いカチオン活性剤系殺菌剤を付着させることも行われているが耐久性に問題がある上に、塵埃を吸着して汚れ現象が目立つ欠点があるとされている。
【0007】
【発明が解決しようとする課題】
ポリエステルをはじめとする合成繊維は、接着剤との親和性が悪いため接着剤併用による殺菌剤固定も不十分であり、繊維仕上げ行程の処理条件に耐え、繊維本来の風合をそこなわず、また十分な耐光性と耐洗濯性を備え、かつ長期間効力を持続し得る合成繊維の衛生加工方法は知られていなかった。
【0008】
【課題を解決するための手段】
本発明者は合成繊維製品に良好な衛生性を付与する方法につき、種々検討し、合成繊維を形成する鎖状高分子の集合体の間隙に殺菌剤を侵入させて固定化させることを試み、耐光、耐洗濯性に優れ、長期間殺菌高価を持続させる本発明の衛生加工法に到達した。すなわち本発明は、合成繊維製品に殺菌剤の水希釈液を付与した後に転写捺染することで殺菌剤を繊維製品に固着することを特徴とする衛生性に優れる合成繊維製品の加工法である。
【0009】
【発明の実施の形態】
本発明方法の対象としては織編物、不織布等、その他の転写捺染可能な全ての合成繊維製品が含まれる。
本発明の繊維製品を構成する合成繊維としては、ポリエステル、ポリアミド、アクリル、アセテートなどの合成繊維であり、これらの中で、ポリエステル、変性ポリエステルが本発明の効果が顕著に発現されるため好ましい。
【0010】
本発明における変性ポリエステル系繊維としては、化1に示したリン含有エステル形成性化合物を練込みあるいは共重合した難燃性ポリエステル繊維、 化2に示したカチオン可染性エステル形成性化合物を共重合したカチオン可染ポリエステル繊維、イソフタル酸を共重合した高収縮ポリエステル、ポリエチレングリコールを練込みあるいは共重合した常圧可染ポリエステル繊維、その他の変性ポリエステル系繊維が含まれる。
【0011】
【化1】
(式中、R1は1価のエステル形成性官能基であり、R2、R3は同じかまたは異なる基であって、それぞれハロゲン原子、炭素原子数1〜10の炭化水素基、R1より選ばれ、Aは2価もしくは3価の有機残基を表わす。またn1は1または2、n2、n3、はそれぞれ0〜4の整数を表わす。)
【0012】
【化2】
【0013】
本発明の衛生性に優れるとは、抗菌性、防臭性、防黴性など微生物から生活環境を衛生的に保つのに優れていることを意味する。
【0014】
本発明の方法に用いる殺菌剤としては親水性の強いもの、着色性のあるもの、臭気または刺激の強いもの、昇華性の強いもの、日光に照射されると変質するもの、毒性が強いもの、塩素を含むもの等を除いてほとんどのものが適用できるが、特に染色不良、退色促進、染料滲出、移染、黄変、異臭等による繊維製品の品位低下を起こさない好ましい殺菌性化合物の例としては、3−メチル−4−イソプロピルフェノール(3M4P)、チモール、p−オキシ安息香酸アルキルエステル(アルキルはメチル、エチル、n−およびiso−プロピル、n−およびsec−またはter−ブチル、ペンチル等)、 グルセリンモノ脂肪酸エステル(脂肪酸はカブリル酸、カブリン酸、ラウリン酸等)、2−(4−チアゾリル)−ベンズイミダゾール(TBZ)、2−メトキシカルボニルアミノベンズイミダゾール(MBC)、2−メトキシカルボニルアミノベンズイミダゾール、4′−n−ドデシルベンゼンスルホン酸塩(MBC-S)、10,10′−オキシビスフェノキシアルシン、8−オキシキノリン銅、キャプタン、ダイホルタン等が挙げられ、2種以上混合してもよく、特に、3M4Pがその加工性、耐久性、安全性等の特性が良く、抗菌剤として好ましい。
【0015】
本発明方法による繊維加工方法は被処理繊維製品に殺菌剤をパティング法、塗布法、浸漬法などで付与した後、片面または両面転写捺染して殺菌剤を転写捺染の加熱により浸透固着させる方法である。この場合処理温度170〜210℃、処理時間20〜70秒から選ばれた条件で処理される。なお、本法では常圧で高温で処理されるので処理温度において蒸気圧が低い殺菌性化合物を選ぶ必要がある。
【0016】
また本発明に係る転写捺染は少なくとも片面、好ましくは両面の転写捺染であり、その両面転写捺染布帛の製造方法は、転写紙に付与された昇華性染料を布帛の両面に昇華転写する方法において、第1の転写紙を前記布帛の片面側に重ね合せ、且つ第2の転写紙を前記布帛の他面側に重ね合せて、少なくとも3層の積層構造とし、該積層構造の両面から圧し付けた状態で加熱して、前記第1、2の転写紙の夫々の昇華性染料を前記布帛の夫々の面に昇華移行させるものである。
【0017】
いずれの方法においても殺菌性化合物が繊維の重量に対して殺菌剤の殺菌効力に応じて0.001〜2.0%の範囲内の所定量以上が繊維内に取り込まれることが必要で、処理方法、使用殺菌剤に応じた有効率(殺菌剤を含む水溶液中の殺菌性化合物が繊維中に取り込まれる割合)を実験的に確認して実際に必要な殺菌剤量が決定される。
【0018】
本発明の方法はポリエステルおよび変性ポリエステル系繊維などの合成繊維高分子の鎖状高分子の集合体の間隙に適切な殺菌性化合物を侵入させて安定に固定化させたもので、効力は長期間安定に持続し優れた耐洗濯性を示す。本発明方法で処理されたポリエステルおよび変性ポリエステル系繊維製品は風合の劣化、撥水性や塵埃吸着性の付与その他変性ポリエステル系繊維の持つ特性(難燃性、カチオン可染性、高収縮性、分散常圧可染性等)を損なう性質が発現することはない。また、吸着された殺菌剤有効成分は究めて微量に抑制されており安全性が高い。
【0019】
また、汎用ポリエステル繊維に対し、変性ポリエステル系繊維は、鎖状高分子の集合体の間隙が多く存在し、そのために殺菌性化合物の固定化率が高く、殺菌性化合物の使用量を極力削減し、廃水中に含まれて排出される殺菌性化合物を最小限に止めることが出来る。
【0020】
【実施例】
次に本発明を実施例により具体的に説明するが、本発明はその要旨を超えない限り以下の実施例に制約されるものではない。なお、実施例中「%」とあるは特に断りない限り「重量%」を示す。
【0021】
実施例1
1.殺菌剤原液処方
(イ) 3−メチル−4−イソプロピルフェノール(3M4P)30%、ジメチルスルホキサイド(DMSO)10%、イソプロパノール20%、ヒマシ油モノエタノールアミン30%、水残量を混合して均一液とした。
(ロ) イルガサンDP-300を20%、DMSOを20%、イソプロパノールを20%、ドデシルベンゼンスルホン液ナトリウム30%、水10%を混合し、均一液とした。
【0022】
2.供試布
変性ポリエステル系布(化1のリン化合物を5モル%共重合した難燃性ポリエステル布)
汎用ポリエステル(ポリエチレンテレフタレート)布
【0023】
3.処理条件
前記殺菌剤原液を10g/lに水で希釈したものに、供試布を浸した後、液の付着率を繊維重量に対して60%に絞り、乾燥した後、表1に示した温度及び時間で供試布を両面転写捺染処理した。 次に還元洗浄〔処理条件;ハイドロサルファイト2g/l、ソーダ灰1g/l70℃、10分間〕を行い風乾した。
4.吸着量分析
供試繊維1gをジクロロメタン50mlに浸漬して超音波振動を与えながら20分間抽出した後ジクロロメタン層を採る。この作業を2回繰り返した後ジクロロメタン層を合わせジクロロメタンを留去した後エタノールで20mlとしてガスクロマトグラフ法により定量した。
表1に試験No.1〜8の各種殺菌剤処理及びその試験布の分析結果について示した。
【0024】
【表1】
本発明の方法による試験No1〜4は殺菌性化合物が検出されたが、対照の温度では検出されなかった(殺菌剤が繊維に吸着されていなかったことが示された。)
また、汎用ポリエステル繊維に対し、変性ポリエステル系繊維の殺菌性化合物吸着量は、約2倍であった。
【0025】
実施例 2
1.供試布
試験No.1〜8はそれぞれ実施例1の試験No.1〜8で処理した変性、及び汎用ポリエステル系布を使用した。各試験布はさらにJAFET標準洗剤を使用し、 JIS L 0217 103号(制菌加工繊維製品一般用途の洗濯方法)により10回洗濯をし、また、 JAFET標準配合洗剤を使用し、厚生省令第13号に準拠(制菌加工繊維製品特定用途の洗濯方法)により50回洗濯を行い抗菌試験に供した。
【0026】
2.抗菌能力試験
黄色ぶどう球菌(ATCC6538P)、肺炎桿菌(ATCC4352)、MRSA(IID1677)を供じて、抗菌能力試験方法としては、JIS L1902-1998準じて実施した。抗菌性は下記式による殺菌活性値で評価する。数値の高いものほど抗菌性に優れている。
殺菌活性値 logA-logC
但し、試験成立条件(logB-logA)>1.5を満たす。
A;未加工標準布の接種直後に回収した菌数の平均値
B; 未加工標準布の18時間培養直後に回収した菌数の平均値
C;加工布の18時間培養直後に回収した菌数の平均値
各試験布の抗菌性能試験結果について表2〜4に示した。
試験結果−1黄色ぶどう球菌(ATCC6538P)
【0027】
【表2】
試験結果−2肺炎桿菌(ATCC4352)
【0028】
【表3】
試験結果−3MRSA(IID1677)
【0029】
【表4】
本発明の方法による供試布は明らかに抗菌効果が認められ、耐洗濯性も優れている。対照は抗菌剤が吸着しておらず抗菌性はまったく認められない。
【0030】
実施例3
1.供試布
試験No.1〜8はそれぞれ実施例1の試験No.1〜8で処理した変性、及び汎用ポリエステル系布を使用した。
2.抗菌効果試験
アスペルギルス ニゲル(A.niger)ATCC6275、ペニシリウム シトリヌム(P.citrinum)ATCC9849、ケトミウム クロボサム(C.globosum)ATCC6205およびミロテシウム ベルカリア(M.verrucaria)USDA1334.2を供試してJIS Z 2911-1976繊維製品のかび抵抗性試験方法ー湿式法に準じて実施した。
試験結果を表5に示した。
【0031】
【表5】
(注) かび抵抗性値
〔3〕 試験片上に菌糸の発育が認められない。
〔2〕 試験片上に菌糸の発育面積が1/3以下。
〔1〕 試験片上に菌糸の発育面積が1/3以上。
本発明の方法による試験No1〜4の供試布はいずれも良好な防黴効果を示した。
【0032】
【発明の効果】
本発明によれば、バインダー樹脂等による風合の硬化がなく、洗濯耐久性が高く、衛生性に優れるポリエステルおよび変性ポリエステル系繊維であるので、家庭用はもちろん、医療機関並びにそれに準ずる施設用として、衣料品(白衣、寝巻など)、寝装品(敷布、布団側地など)、インテリア製品(カーテンなど)、雑貨品(マット、カバーなど)など広範囲な用途に使用することができる。[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a method for processing a synthetic fiber product excellent in hygiene, and more particularly, to a method for immobilizing a bactericidal agent in a polyester and modified polyester fiber structure to give the fiber hygiene.
[0002]
[Prior art]
Socks, underwear, sports clothing, bedding, etc., adhere to the secretions from the user's skin, sweat, exfoliation of the skin, etc., and these serve as nutrients and become a good medium for the growth of microorganisms such as bacteria and mites. Discomfort may be caused by the microbial product, and in some cases may cause infections such as skin diseases. In addition, straw mats, rugs, curtains, wall fabrics, etc., when stored or used in places with high humidity, cause wrinkles and lower the quality due to fiber degradation contamination.
[0003]
Attempts have been made to attach a disinfectant to a textile product in order to keep the textile product hygienic by protecting it from microorganisms such as bacteria, mites, etc., and maintaining good quality, and several methods have been implemented so far. Has been. The most common method is to immerse or spray the textile product in a liquid containing a bactericidal agent. Further, as a method to further strengthen the bactericidal agent fixing, for example, a part of molecules of a bactericidal quaternary ammonium salt is converted into organic silicon. A method of binding to a part of the fiber molecule through a compound, a method of coating and fixing a bactericidal compound such as an organic chlorine compound on the fiber surface with a synthetic resin having a good developability, or an inorganic metal (such as silver) ) Is kneaded into the fiber, or a method of imparting antibacterial properties by combining an organometallic compound in the composition of the fiber material.
[0004]
However, the fibers used as these objects are exclusively cotton, wool, silk, acetate, acrylic, polyamide, vinyl chloride, polyurethane and the like.
[0005]
In principle, these substances have a functional group having the ability to chemically or physically bond with the third substance molecule in the fiber constituting molecule, or those functional group introduced by modification, or the surface of the fiber. The physical properties are excellent in affinity with the synthetic resin adhesive.
[0006]
In addition, a cationic activator-based disinfectant having a high affinity for fibers is generally attached, but there is a problem in durability, and there is a defect that the dirt phenomenon is noticeable by adsorbing dust. Yes.
[0007]
[Problems to be solved by the invention]
Synthetic fibers such as polyester have poor affinity with adhesives, so the disinfectant fixation by adhesives is insufficient, withstands the processing conditions of the fiber finishing process, does not detract from the original texture of the fiber, In addition, there has been no known hygienic processing method for synthetic fibers that has sufficient light resistance and washing resistance and can maintain efficacy for a long period of time.
[0008]
[Means for Solving the Problems]
The present inventor has studied various methods for imparting good hygiene to synthetic fiber products, and tried to inject and fix a fungicide into the gap between the aggregates of chain polymers forming the synthetic fiber, It has reached the sanitary processing method of the present invention that is excellent in light resistance and washing resistance and maintains sterilization cost for a long time. That is, the present invention is a method for processing a synthetic fiber product excellent in hygiene, characterized in that the bactericide is fixed to the fiber product by transfer printing after applying a water-diluted solution of the bactericide to the synthetic fiber product.
[0009]
DETAILED DESCRIPTION OF THE INVENTION
The object of the method of the present invention includes all synthetic fiber products that can be transferred and printed, such as woven and knitted fabrics and nonwoven fabrics.
Synthetic fibers constituting the fiber product of the present invention are synthetic fibers such as polyester, polyamide, acrylic, and acetate. Among these, polyester and modified polyester are preferable because the effects of the present invention are remarkably exhibited.
[0010]
As the modified polyester fiber in the present invention, a flame-retardant polyester fiber kneaded or copolymerized with the phosphorus-containing ester-forming compound shown in Chemical Formula 1, and a cationic dyeable ester-forming compound shown in Chemical Formula 2 are copolymerized. Cation dyeable polyester fibers, high-shrinkage polyester copolymerized with isophthalic acid, atmospheric pressure dyeable polyester fibers kneaded or copolymerized with polyethylene glycol, and other modified polyester fibers.
[0011]
[Chemical 1]
(In the formula, R 1 is a monovalent ester-forming functional group, R 2 and R 3 are the same or different groups, and each is a halogen atom, a hydrocarbon group having 1 to 10 carbon atoms, R 1 A represents a divalent or trivalent organic residue, and n 1 represents 1 or 2, n 2 and n 3 each represents an integer of 0 to 4.)
[0012]
[Chemical 2]
[0013]
The superior hygiene of the present invention means that the living environment is excellently maintained hygienically from microorganisms such as antibacterial, deodorant and antifungal properties.
[0014]
As the bactericidal agent used in the method of the present invention, those having strong hydrophilicity, those having coloring properties, those having strong odor or irritation, those having strong sublimation properties, those that change in quality when exposed to sunlight, those that are highly toxic, Most of them can be applied except those containing chlorine, but especially as examples of preferred bactericidal compounds that do not cause deterioration of the quality of textile products due to poor dyeing, fading promotion, dye leaching, dye transfer, yellowing, nasty smell, etc. Is 3-methyl-4-isopropylphenol (3M4P), thymol, p-oxybenzoic acid alkyl ester (alkyl is methyl, ethyl, n- and iso-propyl, n- and sec- or ter-butyl, pentyl, etc.) Glycerol mono fatty acid ester (fatty acid is cabrylic acid, cabric acid, lauric acid, etc.), 2- (4-thiazolyl) -benzimidazole (TBZ), 2-methoxycarbonylamino Imidazole (MBC), 2-methoxycarbonylaminobenzimidazole, 4'-n-dodecylbenzenesulfonate (MBC-S), 10,10'-oxybisphenoxyarsine, 8-oxyquinoline copper, captan, difortan, etc. Two or more types may be mixed, and 3M4P is particularly preferable as an antibacterial agent because of its good processability, durability, safety and other properties.
[0015]
The fiber processing method according to the present invention is a method in which a bactericidal agent is applied to a fiber product to be treated by a putting method, a coating method, a dipping method, etc., and then single-sided or double-sided transfer printing is performed and the bactericidal agent is permeated and fixed by heating of transfer printing. is there. In this case, the treatment is performed under conditions selected from a treatment temperature of 170 to 210 ° C. and a treatment time of 20 to 70 seconds. In this method, since the treatment is performed at normal pressure and high temperature, it is necessary to select a bactericidal compound having a low vapor pressure at the treatment temperature.
[0016]
The transfer printing according to the present invention is at least one-sided transfer printing, preferably double-sided transfer printing, and the method for producing the double-sided transfer printing fabric is a method of sublimating and transferring a sublimation dye applied to transfer paper onto both sides of the fabric. The first transfer paper was superposed on one side of the fabric and the second transfer paper was superposed on the other side of the fabric to form a laminated structure of at least three layers, and pressed from both sides of the laminated structure. In this state, the sublimation dyes of the first and second transfer papers are sublimated and transferred to the respective surfaces of the fabric.
[0017]
In any method, the bactericidal compound needs to be incorporated into the fiber in a predetermined amount within the range of 0.001 to 2.0% depending on the bactericidal efficacy of the bactericide with respect to the weight of the fiber. The amount of fungicide actually required is determined by experimentally confirming the effective rate according to the agent (ratio in which the fungicidal compound in the aqueous solution containing the fungicide is taken into the fiber).
[0018]
The method of the present invention is a method in which an appropriate bactericidal compound is infiltrated into a gap between a chain polymer aggregate of synthetic fiber polymers such as polyester and modified polyester fiber, and the effect is stable for a long time. It is stable and has excellent washing resistance. Polyester and modified polyester fiber products treated by the method of the present invention have a feeling of deterioration, imparting water repellency and dust adsorbability and other properties of modified polyester fibers (flame retardant, cationic dyeability, high shrinkage, The properties which impair the dispersion normal pressure dyeability, etc.) are not exhibited. Further, the adsorbed active ingredient of the bactericide is controlled to a very small amount and is highly safe.
[0019]
In contrast to general-purpose polyester fibers, modified polyester fibers have many gaps between the aggregates of chain polymers, and therefore, the immobilization rate of the bactericidal compound is high, and the amount of the bactericidal compound used is reduced as much as possible. The bactericidal compounds contained and discharged in the wastewater can be minimized.
[0020]
【Example】
EXAMPLES Next, although an Example demonstrates this invention concretely, this invention is not restrict | limited to a following example, unless the summary is exceeded. In the examples, “%” means “% by weight” unless otherwise specified.
[0021]
Example 1
1. Disinfectant concentrate formulation
(I) 3-methyl-4-isopropylphenol (3M4P) 30%, dimethyl sulfoxide (DMSO) 10%, isopropanol 20%, castor oil monoethanolamine 30%, and the remaining amount of water were mixed to obtain a uniform liquid. .
(B) Irgasan DP-300 20%, DMSO 20%, isopropanol 20%, sodium dodecylbenzenesulfone solution 30% and water 10% were mixed to obtain a uniform solution.
[0022]
2. Test cloth modified polyester cloth (flame retardant polyester cloth copolymerized with 5 mol% of the phosphorus compound of Chemical formula 1)
General-purpose polyester (polyethylene terephthalate) cloth [0023]
3. Treatment conditions After immersing the test cloth in 10 g / l of the bactericide stock solution diluted with water, the adhesion rate of the solution was reduced to 60% with respect to the fiber weight and dried, as shown in Table 1. The test cloth was subjected to double-sided transfer printing at temperature and time. Next, reduction cleaning [treatment conditions: hydrosulfite 2 g / l, soda ash 1 g / l 70 ° C., 10 minutes] was performed and air-dried.
4). Adsorption amount analysis 1 g of test fiber is immersed in 50 ml of dichloromethane and extracted for 20 minutes while applying ultrasonic vibration, and then a dichloromethane layer is taken. After repeating this operation twice, the dichloromethane layers were combined, the dichloromethane was distilled off, and then 20 ml with ethanol was quantified by gas chromatography.
Table 1 shows the various bactericidal treatments of Test Nos. 1 to 8 and the analysis results of the test cloths.
[0024]
[Table 1]
Tests Nos. 1-4 according to the method of the present invention detected a bactericidal compound, but not at the control temperature (showing that the bactericidal agent was not adsorbed to the fiber).
Further, the amount of the sterilizing compound adsorbed by the modified polyester fiber was about twice that of the general-purpose polyester fiber.
[0025]
Example 2
1. The test cloth tests No. 1 to 8 used the modified polyester and the general-purpose polyester cloth treated in Test Nos. 1 to 8 of Example 1, respectively. Each test cloth is further washed with JAFET standard detergent and washed 10 times according to JIS L 0217 103 (washing method for general use of antibacterial processed textile products). Also, JAFET standard combination detergent is used. The product was washed 50 times and subjected to antibacterial tests in accordance with No. 1 (washing method for antibacterial processed textile products specific use)
[0026]
2. The antibacterial ability test was performed according to JIS L1902-1998, using Staphylococcus aureus (ATCC6538P), Neisseria pneumoniae (ATCC4352), and MRSA (IID1677). Antibacterial properties are evaluated by the bactericidal activity value according to the following formula. The higher the number, the better the antibacterial properties.
Bactericidal activity value logA-logC
However, the test establishment condition (logB-logA)> 1.5 is satisfied.
A: Average number of bacteria collected immediately after inoculation of raw standard cloth
B; Average number of bacteria recovered immediately after 18 hours of cultivation of raw standard fabric
C: Average value of the number of bacteria collected immediately after 18 hours of culturing of the processed cloth Tables 2 to 4 show the antibacterial performance test results of each test cloth.
Test result-1 Staphylococcus aureus (ATCC6538P)
[0027]
[Table 2]
Test result-2 Klebsiella pneumoniae (ATCC4352)
[0028]
[Table 3]
Test result-3 MRSA (IID1677)
[0029]
[Table 4]
The test cloth according to the method of the present invention clearly has an antibacterial effect and has excellent washing resistance. In the control, the antibacterial agent was not adsorbed and no antibacterial activity was observed.
[0030]
Example 3
1. The test cloth tests No. 1 to 8 used the modified polyester and the general-purpose polyester cloth treated in Test Nos. 1 to 8 of Example 1, respectively.
2. Antibacterial effect test Aspergillus niger (A.niger) ATCC 6275, Penicillium citrinum (AT. The test was carried out in accordance with the mold resistance test method for products-wet method.
The test results are shown in Table 5.
[0031]
[Table 5]
(Note) Fungus resistance value [3] No hyphal growth is observed on the test piece.
[2] The hyphal growth area on the test piece is 1/3 or less.
[1] The hyphal growth area on the test piece is 1/3 or more.
The test cloths of Test Nos. 1 to 4 according to the method of the present invention all showed a good anti-mold effect.
[0032]
【The invention's effect】
According to the present invention, polyester and modified polyester fiber that has no texture hardening due to a binder resin or the like, has high washing durability, and is excellent in hygiene, so that it can be used not only for home use but also for medical institutions and facilities equivalent thereto. It can be used in a wide range of applications such as clothing (white robes, nightclothes, etc.), bedding (bedclothes, futons, etc.), interior products (curtains, etc.), miscellaneous goods (mats, covers, etc.).
Claims (6)
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26906399A JP3972280B2 (en) | 1999-09-22 | 1999-09-22 | Manufacturing method of synthetic fiber products with excellent hygiene |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26906399A JP3972280B2 (en) | 1999-09-22 | 1999-09-22 | Manufacturing method of synthetic fiber products with excellent hygiene |
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| Publication Number | Publication Date |
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| JP2001089983A JP2001089983A (en) | 2001-04-03 |
| JP3972280B2 true JP3972280B2 (en) | 2007-09-05 |
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| NZ546829A (en) * | 2003-11-26 | 2009-12-24 | Syngenta Participations Ag | Method for controlling fungi and mites in textile substrates |
| JP4813951B2 (en) * | 2006-04-06 | 2011-11-09 | サカイオーベックス株式会社 | Antibacterial fiber structure and method for producing the same |
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1999
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