JP2008115506A - 抗ウイルス性を備えた繊維又は繊維製品及びそれらの製造方法 - Google Patents
抗ウイルス性を備えた繊維又は繊維製品及びそれらの製造方法 Download PDFInfo
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- JP2008115506A JP2008115506A JP2006302013A JP2006302013A JP2008115506A JP 2008115506 A JP2008115506 A JP 2008115506A JP 2006302013 A JP2006302013 A JP 2006302013A JP 2006302013 A JP2006302013 A JP 2006302013A JP 2008115506 A JP2008115506 A JP 2008115506A
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- Prior art keywords
- acid
- fiber
- virus
- antiviral
- product
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- 235000019265 sodium DL-malate Nutrition 0.000 description 1
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 1
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- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
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- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
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- 235000019983 sodium metaphosphate Nutrition 0.000 description 1
- 235000019795 sodium metasilicate Nutrition 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
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- 235000011008 sodium phosphates Nutrition 0.000 description 1
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- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
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- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
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- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- GRPURDFRFHUDSP-UHFFFAOYSA-N tris(prop-2-enyl) benzene-1,2,4-tricarboxylate Chemical compound C=CCOC(=O)C1=CC=C(C(=O)OCC=C)C(C(=O)OCC=C)=C1 GRPURDFRFHUDSP-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
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Abstract
【解決手段】本発明の繊維用抗ウイルス加工剤は、ポリ−オキシエチレン(ジメチルイミノ)エチレン(ジメチルイミノ)エチレンジクロライドを含有する。繊維又は繊維製品を繊維用抗ウイルス加工剤で処理し、次いでソーピングすることにより、繊維又は繊維製品に優れた抗ウイルス性を付与することができる。
【選択図】 なし
Description
項1.PMIECを含有する繊維用抗ウイルス加工剤。
項2.(1)PMIEC及び(2)被膜を形成し得る化合物を含有する繊維用抗ウイルス加工剤。
項3.繊維又は繊維製品を項1又は項2に記載の繊維用抗ウイルス加工剤で処理し、次いでソーピングして得られる、抗ウイルス性を備えた繊維又は繊維製品。
項4.繊維又は繊維製品に(1)PMIEC及び(2)被膜を形成し得る化合物を付着及び/又は含浸させ、次いで熱処理し、ソーピングすることにより、抗ウイルス性を備えた繊維又は繊維製品を製造する方法。
本発明の繊維用抗ウイルス加工剤は、PMIECを含有する。
ポリカルボン酸としては、例えば分子中に少なくとも2個のカルボキシル基を有するポリカルボン酸を使用することができる。このようなポリカルボン酸としては、少なくとも2個のカルボキシル基を有するポリカルボン酸である限り従来公知のものを広く使用でき、例えば各種の脂肪族ポリカルボン酸、脂環族ポリカルボン酸、芳香族ポリカルボン酸等が挙げられる。これらカルボン酸は、水酸基、ハロゲン基、カルボニル基、炭素−炭素二重結合を有していても差し支えない。
(b) アルデヒド化合物
アルデヒド化合物としては、例えばホルムアルデヒド、ジアルデヒド(グリオキザール)等が挙げられる。
(c) N−メチロール化合物
N−メチロール化合物としては、例えばジメチロール尿素及びそのメチル化物、ジメチロールエチレン尿素及びそのメチル化物、ジメチロールウロン及びそのメチル化物、ジメチロールトリアゾン及びそのメチル化物、ジメチロールプロピレン尿素及びそのメチル化物、ジメチロールジヒドロキシエチレン尿素、メチル化ジメチロールジメトキシエチレン尿素、1,3−ジメチル−4,5−ジヒドロキシエチレン尿素及びそのメチル化物、ジメチロール−4−メトキシ−5,5−ジメチルプロピレン尿素及びそのメチル化物、ジメチロールアルキルカーバメイト及びそのメチル化物、テトラメチロールグリオキザールモノウレイン及びそのメチル化物等が挙げられる。
(d) 分子内にエポキシ基(グリシジル基)を有する化合物
分子内にエポキシ基(グリシジル基)を有する化合物としては、例えば脂肪族エポキシ化合物、ジグリシジル化合物、トリグリシジル化合物、ポリグリシジル化合物、脂環式エポキシ化合物、異節環状型エポキシ化合物、活性ビニル化合物の他、ビスフェノールA−エピクロルヒドリン化合物、ビスフェノールA−ジグリシジルエーテル化合物及びそのエチレンオキシド付加物又はプロピレンオキシド付加物、ビスフェノールF−ジグリシジルエーテル化合物、水素化ビスフェノールA−ジグリシジルエーテル化合物、水素化ビスフェノールF−ジグリシジルエーテル化合物等が挙げられる。
で表されるジグリシジルエーテルを挙げることができ、具体的にはエチレングリコールジグリシジルエーテル、ジエチレングリコールジグリシジルエーテル、トリエチレングリコールジグリシジルエーテル、ポリエチレングリコールジグリシジルエーテル(n=4〜50)、プロピレングリコールジグリシジルエーテル、ジプロピレングリコールジグリシジルエーテル、トリプロピレングリコールジグリシジルエーテル、ポリプロピレングリコールジグリシジルエーテル(n=4〜50)、ネオペンチルグリコールジグリシジルエーテル、1,6−ヘキサンジオールジグリシジルエーテル、グリセロールジグリシジルエーテル、ジグリシジルポリシロキサン等が挙げられる。
(e) 分子内にビニル基を有する化合物
分子内にビニル基を有する化合物としては、例えば分子内にジアクリロイル基を有する化合物、分子内にジメタクリロイル基を有する化合物、分子内にトリアリル基を有する化合物、分子内にテトラアリル基を有する化合物、分子内にペンタアリル基を有する化合物等を挙げることができる。
(f) イソシアネート化合物
イソシアネート化合物としては、例えばジイソシアネート化合物、トリイソシアネート化合物、ポリイソシアネート化合物等の他、m−イソプロペニル−α,α−ジメチルベンジルイソシアネート等を挙げることができる。
(g) メラミン化合物
メラミン化合物としては、例えば、メラミン、トリメチロールメラミン、ヘキサメチロールメラミン及びこれらのメチル化物等が挙げられる。
本発明における繊維は、合成繊維、再生繊維及び天然繊維のいずれでもよい。
抗ウイルス性を備えた繊維又は繊維製品は、処理されるべき繊維又は繊維製品に、本発明の繊維用抗ウイルス加工剤を付着及び/又は含浸させ、次いで熱処理し、ソーピングすることにより製造される。
目付150g/m2の綿織物を精練し、漂白し、シルケット処理を行った。次いで、処理後の綿織物を、ポリオキシエチレン(ジメチルイミノ)エチレン(ジメチルイミノ)エチレンクロライド1.5重量%、メラミン樹脂(リケンレジンMM65S、三木理研工業製)1重量%及び触媒(リケンフィクサーRC−3、三木理研工業製)0.5重量%を含む水溶液に浸漬し、マングルで絞り(絞り率60%)、100℃で乾燥し、160℃で2分間熱処理を行った。熱処理後の綿織物を、以下「綿織物A」という。更に、綿織物Aを、ノニオン界面活性剤(商品名:ソフタノール90、日本触媒製)0.05重量%を含む水溶液を使用して40℃で5分間ソーピングを行い、次に5分間水洗することにより、綿織物を得た。ソーピング及び水洗処理して得られる本発明の綿織物を、以下「綿織物B」という。
目付150g/m2の綿織物を精練し、漂白し、シルケット処理を行った。次いで、処理後の綿織物を、ノニオン界面活性剤(商品名:ソフタノール90、日本触媒製)0.05重量%を含む水溶液を使用して40℃で5分間ソーピングを行い、次に5分間水洗することにより、綿織物を得た。
目付150g/m2の綿織物を精練し、漂白し、シルケット処理を行った。次いで、処理後の綿織物を、メラミン樹脂(リケンレジンMM65S、三木理研工業製)1重量%及び触媒(リケンフィクサーRC−3、三木理研工業製)0.5重量%を含む水溶液に浸漬し、マングルで絞り(絞り率60%)、100℃で乾燥し、160℃で2分間熱処理を行った。更に、上記処理した綿織物を、ノニオン界面活性剤(商品名:ソフタノール90、日本触媒製)0.05重量%を含む水溶液を使用して40℃で5分間ソーピングを行い、次に5分間水洗することにより、綿織物を得た。
目付150g/m2の綿織物を精練し、漂白し、シルケット処理を行った。次いで、処理後の綿織物を、2−ピリジンチオール−ジンク−1−オキシド1重量%、メラミン樹脂(リケンレジンMM65S、三木理研工業製)1重量%及び触媒(リケンフィクサーRC−3、三木理研工業製)0.5重量%を含む水溶液に浸漬し、マングルで絞り(絞り率60%)、100℃で乾燥し、160℃で2分間熱処理を行った。更に、熱処理後の綿織物を、ノニオン界面活性剤(商品名:ソフタノール90、日本触媒製)0.05重量%を含む水溶液を使用して40℃で5分間ソーピングを行い、次に5分間水洗することにより、綿織物を得た。
目付150g/m2の綿織物を精練し、漂白し、シルケット処理を行った。次いで、処理後の綿織物を、酸化亜鉛1重量%及びアクリル酸樹脂(商品名:MAR、松本油脂製薬(株)製)2重量%を含む水溶液に浸漬し、マングルで絞り(絞り率60%)、100℃で乾燥し、160℃で2分間熱処理を行った。更に、熱処理後の綿織物を、ノニオン界面活性剤(商品名:ソフタノール90、日本触媒製)0.05重量%を含む水溶液を使用して40℃で5分間ソーピングを行い、次に5分間水洗することにより、綿織物を得た。
(1)ウイルス液の調製
鳥インフルエンザウイルス(A/budgeringer/Aichi/1/77(H3N8))を発育鶏卵の尿膜腔内に接種し、35℃で3日間培養後に、尿膜腔液を採取し、ウイルス液として使用した。
実施例1で得られた綿織物A、綿織物B及び綿織物C(各綿織物の大きさは18mm×18mm)を121℃のオートクレーブ中に20分間入れ、次に乾燥させた。3枚の綿織物Aを1組とし、2組(計6枚)を試験に使用した。また、上記と同様に、3枚の綿織物Bを1組、3枚の綿織物Cを1組とし、これら各々2組を試験に使用した。更に、比較のために、未処理の綿織物、比較例1〜4で得られた綿織物及び比較例1〜4で得られた綿織物を50回洗濯した綿織物についても、上記と同様にして試験に使用した。
各々の綿織物1組(3枚)をマイクロチューブに入れ、ウイルス液0.1mlを浸み込ませ、室温で10分間感作させた。感作後、直ちにマイクロチューブを1分間当たり5000回転の速度で30秒間回転させ、各々の綿織物から感作ウイルス液を回収した。
回収した各感作ウイルス液を、直ちにPBSを用いて10倍段階希釈し、48穴マイクロプレートで培養した初代鶏腎細胞に接種し(0.1ml/ウエル、2ウエル)、37℃で1時間保持し、感作ウイルスを初代鶏腎細胞に吸着させた後、増殖培地(ダルベッコ変法イーグル培地に、10%牛血清、10%トリプトース・ホスフェート・ブロスを加えたもの)0.2mlを加え、37℃で培養し、翌日増殖培地を交換し、更に6日間(計7日間)培養を行った。
綿織物B及び綿織物Cで感作させた後に回収されたウイルス液中に残存するウイルス感染価は、いずれも検出限界以下10≦0.5であり、洗濯を50回繰り返してもその抗ウイルス効果が低下しないことが確認できた。
Claims (4)
- ポリ−オキシエチレン(ジメチルイミノ)エチレン(ジメチルイミノ)エチレンジクロライドを含有する繊維用抗ウイルス加工剤。
- (1)ポリ−オキシエチレン(ジメチルイミノ)エチレン(ジメチルイミノ)エチレンジクロライド及び(2)被膜を形成し得る化合物を含有する繊維用抗ウイルス加工剤。
- 繊維又は繊維製品を請求項1又は請求項2に記載の繊維用抗ウイルス加工剤で処理し、次いでソーピングして得られる、抗ウイルス性を備えた繊維又は繊維製品。
- 繊維又は繊維製品に(1)ポリ−オキシエチレン(ジメチルイミノ)エチレン(ジメチルイミノ)エチレンジクロライド及び(2)被膜を形成し得る化合物を付着及び/又は含浸させ、次いで熱処理し、ソーピングすることにより、抗ウイルス性を備えた繊維又は繊維製品を製造する方法。
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JP7073593B1 (ja) * | 2022-01-19 | 2022-05-23 | 大木 彬 | 抗菌、抗カビ、抗ウイルス性消毒剤組成物 |
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WO2010147165A1 (ja) | 2009-06-16 | 2010-12-23 | 積水化学工業株式会社 | Rnaウイルス感染阻止剤、rnaウイルス感染阻止方法、rnaウイルス感染阻止製品及びrnaウイルス感染阻止剤としての使用 |
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WO2017171066A1 (ja) * | 2016-03-31 | 2017-10-05 | 積水化学工業株式会社 | 抗菌抗ウイルス性組成物 |
JPWO2017171066A1 (ja) * | 2016-03-31 | 2018-04-05 | 積水化学工業株式会社 | 抗菌抗ウイルス性組成物 |
CN108366560A (zh) * | 2016-03-31 | 2018-08-03 | 积水化学工业株式会社 | 抗菌抗病毒性组合物 |
CN112042644A (zh) * | 2016-03-31 | 2020-12-08 | 积水化学工业株式会社 | 抗菌抗病毒性组合物 |
CN112042644B (zh) * | 2016-03-31 | 2022-03-11 | 积水化学工业株式会社 | 抗菌抗病毒性组合物 |
JP7073593B1 (ja) * | 2022-01-19 | 2022-05-23 | 大木 彬 | 抗菌、抗カビ、抗ウイルス性消毒剤組成物 |
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