TW201138627A - Composition, antibacterial processing agent and antibacterial molded article - Google Patents

Composition, antibacterial processing agent and antibacterial molded article Download PDF

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Publication number
TW201138627A
TW201138627A TW99140079A TW99140079A TW201138627A TW 201138627 A TW201138627 A TW 201138627A TW 99140079 A TW99140079 A TW 99140079A TW 99140079 A TW99140079 A TW 99140079A TW 201138627 A TW201138627 A TW 201138627A
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antibacterial
composition
agent
treatment agent
doc
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TW99140079A
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Chinese (zh)
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Naoto Horita
Masashi Sakamoto
Nobuo Kusamoto
Shuichi Murakami
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Idemitsu Technofine Co Ltd
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/781,3-Thiazoles; Hydrogenated 1,3-thiazoles

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Disclosed is a composition which contains two kinds of imidazole-based organic antibacterial agents and an antiallergic agent. The composition therefore suppresses the production of causes of allergy-causing substances, namely bacteria, fungi and mites and provides a practical allergy deactivation performance even in cases where the amount of a deactivation agent for allergy-causing substances is reduced. Consequently, the composition enables reduction of the amount of a deactivation agent for allergy-causing substances, and an antibacterial molded article that contains the composition or antibacterial processing agent of the present invention can have a good texture and does not easily suffer from discoloration due to light or heat.

Description

201138627 六、發明說明: 【發明所屬之技術領域】 本發明係關於一種組合物、抗菌性處理劑及抗菌性成形 品° 【先前技術】 先前’有具有抗菌性、防黴菌性、防蟎蟲性、抗過敏性 之組合物’及由該組合物加工而成之加工成形品等。 例如有將含有硼之組合物捏合入樹脂而成之抗菌防蟎蟲 性樹脂組合物(文獻1 :日本專利特開2005-29451號公報)。 又’亦有含有具有殺蜗蟲性及殺菌性之苯并咪唾系化合物 的除蟲劑(文獻2 :曰本專利特開昭59-65065號公報、文獻 3 :日本專利特開昭59-172477號公報)。此外,亦有含有包 含無機固體酸之抗過敏劑的抗過敏原製品(文獻4:日本專 利特開2003-81727號公報、文獻5:國際公開〇9/〇44648號 公報)。 然而,文獻1至5中所記載之組合物等無法全部滿足抗菌 性、防黴菌性、防蟎蟲性、抗過敏性。又,於組合物中含 有抗過敏劑之情形時,若抗過敏劑之含量過多,則將組合 物加工為成形品時,有存在如下問題之虞:成形品之質地 下降,或易發生由光、熱引起之變色。 【發明内容】 本發明之目的在於提供一種具有抗菌性、防黴菌性、防 蜗蟲性、抗過敏性之組合物,抗菌性處理劑及抗菌性成形 品,即使抗過敏劑之含量較少亦發揮出實用上充分之抗過 152257.doc 201138627 敏性能。 (!)本發明之組合物,其特徵在於:含有包含選自咪唑系 之有機系抗菌劑中之至少2種的抗菌性組合物、與過敏誘 發物質之去活化劑。 (2) 此處,上述咪唑系之有機系抗菌劑較佳為具有笨并咪 坐環及噻唑基之化合物、與具有苯并咪唑環及胺基甲酸酯 基之化合物。 (3) 並且,本發明之組合物較佳為含有無機系抗菌劑。 (4) 此處,上述無機系抗菌劑較佳為載銀磷酸錯。 (5) 進而’本發明之組合物較佳為含有除蟎蟲劑。 (6) 此處,上述除蟎蟲劑較佳為氧化硼或含有其之玻螭 質。 ' (7) 又,上述過敏誘發物質之去活化劑較佳為源自天然之 多酚類、合成高分子酚、及無機固體酸中之.至少任一種。 (8) 本發明之抗菌性處理劑,其特徵在於:含有上述組合 物與分散介質》 (9) 此處,本發明之抗菌性處理劑較佳為含有黏合樹脂。 (10) 又’本發明之抗菌性處理劑較佳為含有交聯劑。 (11) 並且’上述抗菌性處理劑較佳為生活用喷霧劑、塗 料、塗布劑、表面處理劑、及纖維處理劑中之任一種。 (12) 本發明之抗菌性成形品’其特徵在於:其係利用上述 抗菌性處理劑,對纖維、布帛、樹脂膜、將纖維或布帛積 層於樹脂膜上而成之積層體中之任一者進行處理而成者。 (13) 又’本發明之抗菌性成形品,其特徵在於:其係對含 152257.doc 201138627 有上述組合物與樹脂之混合物進行成形而成者。 根據本發明之組合物及抗菌性處理劑,藉由將抗菌性組 合物及過敏誘發物質之去活化劑組合,可發揮出抗菌性、 防黴菌性、防蟎蟲性、抗過敏性。又,由於可抑制作為過 敏誘發物質之成因之細菌、㈣、蜗蟲之產生,故而即使 過敏誘發物質之去活化劑之含量較少,亦可獲得實用之過 敏去活化性能。因此’可使本發明之組合物及抗菌性處理 劑之過敏誘發物質之去活化劑之含量為少量,且可使含有 本發明之組合物或抗菌性處理劑之抗菌性成形品成為質地 良好’不易發生由光、熱引起之變色者。 【實施方式】 以下,對用以實施本發明之形態進行詳細說明。 (組合物之構成) 本發明之組合物含有包含選自味嗤系之有機系抗菌劑_ 之至少2種的抗菌性組合物、與過敏誘發物質之去活化离 (以下有時簡稱為「抗過敏劑」)。 作為有機系抗菌劑,例如可列棗. 仆人& 1 本并W胺基甲酸®201138627 VI. Description of the Invention: [Technical Field] The present invention relates to a composition, an antibacterial treatment agent, and an antibacterial molded article. [Prior Art] Previously, it has antibacterial, antifungal, and anti-mite properties. The anti-allergic composition 'and the processed molded article processed from the composition. For example, there is an antibacterial and anti-mite resin composition obtained by kneading a composition containing boron into a resin (Document 1: Japanese Patent Laid-Open Publication No. 2005-29451). Further, there are also insecticides containing a benzopyrene compound having a snail-killing and bactericidal property (Document 2: Japanese Patent Laid-Open Publication No. SHO 59-65065, Document No. 3: Japanese Patent Laid-Open No. 59-- Bulletin No. 172477). Further, there is also an antiallergen product containing an anti-allergic agent containing an inorganic solid acid (Document 4: Japanese Laid-Open Patent Publication No. 2003-81727, and Document 5: International Publication No. 9/44648). However, the compositions and the like described in Documents 1 to 5 cannot all satisfy the antibacterial property, the antifungal property, the anti-mite property, and the anti-allergic property. Further, when the anti-allergic agent is contained in the composition, when the content of the anti-allergic agent is too large, when the composition is processed into a molded article, there is a problem that the texture of the molded article is lowered or light is likely to occur. Heat caused by discoloration. SUMMARY OF THE INVENTION An object of the present invention is to provide a composition having antibacterial property, antifungal property, anti-cogwheel resistance and anti-allergic property, an antibacterial treatment agent and an antibacterial molded product, even if the anti-allergic agent is contained in a small amount. Play a practically full resistance to 152257.doc 201138627 sensitive performance. (!) The composition of the present invention contains an antibacterial composition containing at least two selected from the group consisting of imidazole-based organic antibacterial agents, and a deactivating agent for an allergy-inducing substance. (2) Here, the above-mentioned imidazole-based organic antibacterial agent is preferably a compound having a stilbene ring and a thiazolyl group, and a compound having a benzimidazole ring and a urethane group. (3) Further, the composition of the present invention preferably contains an inorganic antibacterial agent. (4) Here, the inorganic antibacterial agent is preferably a silver-loaded phosphoric acid. (5) Further, the composition of the present invention preferably contains an insecticide. (6) Here, the above-mentioned aphid removing agent is preferably boron oxide or a cellulose containing the same. Further, the deactivating agent for the allergy-inducing substance is preferably at least one selected from the group consisting of natural polyphenols, synthetic polymeric phenols, and inorganic solid acids. (8) The antibacterial treatment agent of the present invention comprising the above composition and a dispersion medium (9) Here, the antibacterial treatment agent of the present invention preferably contains a binder resin. (10) Further, the antibacterial treatment agent of the present invention preferably contains a crosslinking agent. (11) Further, the antibacterial treatment agent is preferably any of a domestic spray, a coating, a coating agent, a surface treatment agent, and a fiber treatment agent. (12) The antibacterial molded article of the present invention is characterized in that the fiber, the cloth, the resin film, and the layered body in which the fiber or the cloth is laminated on the resin film is used by the antibacterial agent. The person who handles it. (13) The antibacterial molded article of the present invention, which comprises a mixture of the above composition and a resin comprising 152257.doc 201138627. According to the composition of the present invention and the antibacterial treatment agent, the antibacterial property, the antifungal property, the anti-mite property, and the anti-allergic property can be exhibited by combining the antibacterial composition and the deactivating agent of the allergy-inducing substance. Further, since bacteria, (4), and worms, which are causes of the allergen-inducing substance, can be suppressed, practical desensitization deactivation performance can be obtained even if the content of the deactivating agent of the allergy-inducing substance is small. Therefore, the content of the deactivating agent of the allergy-inducing substance of the composition of the present invention and the antibacterial treatment agent can be made small, and the antibacterial molded article containing the composition of the present invention or the antibacterial treatment agent can be made into a good texture. It is not easy to cause discoloration caused by light or heat. [Embodiment] Hereinafter, embodiments for carrying out the invention will be described in detail. (Composition of the composition) The composition of the present invention contains an antibacterial composition containing at least two kinds of organic antibacterial agents selected from the group consisting of miso-type, and deactivation of the allergic-inducing substance (hereinafter sometimes referred to simply as "anti- Allergic agent"). As an organic antibacterial agent, for example, jujube can be listed. Servant & 1 and W-carbamic acid®

二:Γ原子之苯—、笨并味唾之㈣I 二:丁生物荨。作為該有機系抗菌劑,較佳為具有苯并巧 基之化合物。 …、有本…環及胺基甲❹Two: benzene of the cesium atom, stupid and smelly (four) I two: Ding biological 荨. As the organic antibacterial agent, a compound having a benzo compound is preferred. ..., has this ring and aminomethine

作為笨并咪錢基甲酸酷化合物,例如可列H =咪。坐胺基甲酸曱酿、,丁基胺甲酿基 胺基甲酸曱酯、6_苯甲 并+ 丞2本开咪唑胺基甲酸〗 152257.doc 201138627 酯、6-(2-噻吩羰基)-1H-2-苯并咪唑胺基甲酸甲酿等。 作為含硫原子之苯并咪。坐化合物’例如可列舉:1 Η—] 硫氰基曱基硫代苯并咪唑、1_二曱基胺基磺醯基_2_氰基_ 4-溴-6-三氟甲基苯并咪唑等。 作為本并味《«坐之環式化合物衍生物,例如可列舉:2_(4 噻唑基)-1Η-苯并咪唑、2-(2-氣苯基)_1Η·笨并咪唑、2·(1_ (3,5-二甲基吡唑基))_1Η•苯并咪唑、2_(2_呋喃基)ih笨并 咪唑等。 該等有機系抗菌劑中,尤佳為2_(4_噻唑基)·1Η·苯并咪 唾與1Η-2-苯并味。坐胺基甲酸曱酿之2種。藉由併用該等不 同之2種’可針對微生物獲得抗菌作帛及防黴菌作用之優 異相乘效果,並且亦可獲得防蟎蟲作用。 酸曱酯之調配比例以質量比計,較佳為丨:丨至5 又,2-(4-嗟唾基)-1Η-苯并咪唾與汨_2_苯并咪唾胺基甲 此處,若2-(4_噻唑基)-1Η·笨并咪唑與m -2-苯并味唾胺As a stupid compound, such as H = Mi. Sodium carbamic acid broth, butyl melamine carboxylic acid decyl methacrylate, 6 benzophenone + hydrazine 2 imidazolidine carboxylic acid 〗 152257.doc 201138627 ester, 6-(2-thiophenecarbonyl)- 1H-2-benzimidazolyl carbamate, etc. As a sulfur atom, benzopyrene. The compound can be exemplified by: 1 Η-] thiocyanothio thiobenzimidazole, 1-didecylaminosulfonyl-2-cyano-4-bromo-6-trifluoromethylbenzo Imidazole and the like. As a derivative of the present invention, for example, 2-(4-thiazolyl)-1Η-benzimidazole, 2-(2-phenylphenyl)_1Η·benzimidazole, 2·(1_ (3,5-Dimethylpyrazolyl)) Η Η • benzimidazole, 2 —( 2 —furanyl)ih benzoimidazole, and the like. Among these organic antibacterial agents, 2_(4-thiazolyl)·1Η·benzoimin and 1Η-2-benzo are particularly preferred. Take 2 kinds of carbamic acid. By using these two different kinds, the superior multiplication effect of the antibacterial action and the antifungal action can be obtained for the microorganism, and the anti-mite effect can also be obtained. The ratio of the acid ester is preferably 丨: 丨 to 5, and 2-(4-嗟-saltyl)-1Η-benzopyrene and 汨_2_benzoimylamamine Where, if 2-(4-thiazolyl)-1Η·stupid imidazole and m-2-benzene succinylamine

量增大之虞。The amount of increase.

酿、及無機固體酸等,亦可含有複數種該Brewed, and inorganic solid acid, etc., may also contain a plurality of

糖、薑黃素、香豆素等。 I52257.doc 201138627 作為合成高分子酚,例如可列舉:聚聯笨酚、聚乙烯酚 等。 作為無機固體酸,例如可列舉:磷酸鋁等磷酸金屬化合 物,Η取代Y型等之沸石,銻酸,Si〇2_A12〇3等複合氧化 物,矽酸鎂,磷酸锆、氧化锆、碳酸锆銨或碳酸锆鉀等锆 化合物、及無機離子交換物等。 並且,本發明之組合物之抗菌性組合物與抗過敏劑之調 配比例以質量比計’較佳為3 :丨至丨:5,尤佳為丨:3。若 抗過敏劑之調配比例大於上述範圍,則由組合物加工為成 形品時,成形品之質地會降低,變得易發生由光、熱引起 之變色。另一方面,若抗過敏劑之調配比例小於上述範 圍’則變得無法獲得實用之過敏去活化性能。 藉由設為如此之特定質量比,可效率更加良好地發揮出 抗菌性、防黴菌性、防蟎蟲性,其結果為,即使抗過敏劑 之含量較少,亦可製成具有實用之抗過敏性的組合物。 本發明之組合物尤佳為除含有上述抗菌性組合物及上述 抗過敏劑以外’亦含有無機系抗菌劑與除蟎蟲劑。 作為無機系抗菌劑,例如可列舉:硫酸銅等銅化合物、 氧化鋅等鋅化合物、鎳化合物、銅-鎳合金等無機金屬化 合物、承載有金屬之沸石、或作為其鹽之磷酸锆等,尤佳 為承載有銀之磷酸鍅(載銀磷酸锆載銀磷酸锆之抗菌速 度快’於抗菌性及防黴菌性方面優異。 又’於本發明之組合物除含有抗菌性組合物與抗過敏劑 以外’亦含有無機系抗菌劑之情形時,抗菌性組合物與無 152257.doc 201138627 機系抗菌劑之調配比例以質量比計,較佳為1 . 1至5 . 1, 尤佳為2 : 1。 藉由設為如此之特定質量比,可藉由更少之組合物之添 加量而獲得質地良好,不易發生由光、熱引起之變色的抗 菌性成形品,並且可效率良好地獲得藉由併用咪唑系之有 機系抗菌劑與無機系抗菌劑而產生之顯著之抗菌作用之相 乘效果。 作為除蟎蟲劑,例如可列舉氧化硼或含有其之玻璃質 等。由於氧化硼或含有其之玻璃質為無機化合物,故而可 獲得與有機化合物相比,不易發生變色,不易發生由光、 熱引起之變色的抗菌性成形品,因而較佳。 進而,於本發明之組合物除含有抗菌性組合物與抗過敏 劑以外,亦含有除蟎蟲劑之情形時,抗菌性組合物與除蟎 蟲劑之調配比例以質量比計,較佳為1 : 1至1 : 5,尤佳為 1 : 3 c 藉由設為如此之特定質量比,可藉由較少之組合物之添 加量製成防蟎蟲性優異之抗菌性成形品。 本發明之組合物對表1至表5所示之微生物即菌類(真菌 類、細菌類等)具有抗菌性及防黴菌性。 [表1] 真 菌 類 1 鏈格孢菌 Altemaria altemata 2 泡盛趟菌 Aspergillus awamori 3 黑麴菌 Aspergillus niger 4 米麴菌 Aspergillus oryzae 5 黃麴菌 Aspergillus flavus I52257.doc 201138627 6 雜色魏菌 Aspergillus versicolor 7 煙麴菌 Aspergillus fumigatus 8 小巢狀麴菌 Aspergillus nidulans 9 灰帶藍麴菌 Aspergillus glaucus 10 土麴菌 Aspergillus terreus 11 海棗麴菌 Aspergillus phoenjcus 12 溜麴菌 Aspergillus tamari 13 文氏麴菌 Aspergillus wentii 14 侷限麴菌 Aspergillus restrictus 15 褚麴菌 Aspergillus ochraceus 16 棒趨菌 Aspergillus clavatus 17 焦麴菌 Aspergillus ustus 18 亮白麴菌 Aspergillus candidus 19 寄生鲍菌 Aspergillus parasiticus 20 傘枝犁頭黴 Absidia corymbifera 21 琉球麴菌 Aspergillus luchensis 22 灰綠犁頭黴 Absidia glauca 23 細極鏈格抱菌 Altemaria tenuis 24 豌豆鏈格孢菌 Altemaria pisi 25 亮白鍵格抱菌 Altemaria candidus 26 芸苔鏈格孢菌 Altemaria brassicicola 27 出芽短梗黴 Aureobasidium pullulans 28 蜂囊菌 Ascosphaera apis 29 螺殼狀絲囊黴 Aphanomyces cochlioides 30 蘿蔔絲囊黴菌 Aphanomyces raphani 31 灰黴菌 Botrytis cinerea 32 絲衣黴 Byssochlamys nivea 33 白色念珠菌 Candide albicans 34 甜菜尾孢菌 Cerespora beticola 35 香蕉尾孢菌 Cerespora musao 36 麥角菌 Claviceps purpurea 37 三葉草刺盤孢菌 Colletotrichum trifolii 38 地衣長嗓殼菌 Ceratocystis cora 39 球毛殼菌 Chaetomium globosum 40 芽枝狀枝孢菌 Cladosporium cladosporioides 41 膝曲彎孢菌 Curvularia geniculata 42 嗜熱金色孢 Chrysosporium thermophilum 43 高裡念珠菌 Candida guilliermondii 44 解脂念珠菌 Candida lipolytica 45 菌膜念珠菌 Candida pelliculose 152257.doc -9- 201138627 46 熱帶念珠菌 Candida tropicalis 47 充髮念珠菌 Candida glabrata 48 Candida acutus 49 產朊念珠菌 Candida utilis 50 球孢枝孢菌 Cladosporium sphaerospermum 51 蠟葉枝孢菌 Cladosporium herbarum 52 稻白絹病菌 Corticium rolfsii 53 番另5炭症病菌 Colletotrichum phomoides 54 草每炭症病菌 Colletotrichum fragariae 55 馬鈐薯炭疽病菌 Colletotrichum atramentarium 56 菜豆炭疽病菌 Colletotrichum lindemuthianum 57 榆枯萎病菌 Ceratocystis ulmi 58 丙酮丁酵梭桿菌 Clostridium acetobutylicum 59 產芽孢梭菌 Clostridium sporogenes 60 梅黑星病菌 Cladosporium carpophilum 61 彎孢菌 Curvularia lunata 62 嗜毛金色孢 Chrysosporium keratinophilum 63 淺黃隱球菌 Cryptococcus lutealus 64 新型隱球菌 Cryptococcus neoformans 65 樹脂枝孢黴 Cladosporium resinae 66 淺白隱球菌 Cryptococcus albidas 67 綠毛殼菌 Chaetomium clivaceum 68 樹狀指孢徽 Dactylium derdroides 69 黑色蒂腐病菌 Diplodia natalensis 70 澳洲德氏黴 Drechslera australiensis [表2] 真 71 高滲散囊菌 Eurotium tonophilum 菌 72 紫附球菌 Epicoccum purpurascens 類 73 匍匐散囊菌 Eurotium repens 74 赤散囊菌 Eurotium rubrum 75 謝瓦散囊菌 Eurotium chevalieri 76 阿姆斯特丹散囊菌 Eurotium amstelodami 77 構巢裸胞殼 Emericella nidulans 78 甄氏外瓶黴 Exophiale jeanselmei 79 半裸鐮刀菌 Fusarium semitectum 80 尖孢鐮刀菌 Fusarium oxysporum 81 Fusarium voseum 82 串珠鐮刀菌 Fusarium moniliforme 152257.doc -10- 201138627 83 腐皮鎌刀菌 Fusarium solani 84 粉紅鐮刀菌 Fusarium roseum 85 雪腐鐮刀菌 Fusarium nivale 86 燕麥鐮刀菌 Fusarium avenaceum 87 銳頂鐮刀菌 Fusarium acuminatum 88 再育鐮刀菌 Fusarium proliferatum 89 禾穀鐮刀菌 Fusarium graminearum 90 棉花根腐病菌 Fhymatotricum omnivorum 91 白地徽:菌 Geotricham candidum 92 Geotricham lactus 93 黏帚黴菌 Gliocladium virens 94 檬果炭疽病菌 Glomerella cingulata 95 長蠕孢黴 Helminthosporium sp. 96 佩德羅縮氏著色芽生菌 Hormoderdrum pedrosoi 97 稗草生防潛力菌 Helminthosporium gramineum 98 革橺菌 Lenzites trabea 99 木材腐朽菌 Lenzites trabae 100 潔麗香菇 Lentinus lepideus 101 足腫分支菌 Medurella mycetomii 102 犬小芽胞菌 Microsporum canis 103 石膏樣小芽胞菌 Microsporum gypseum 104 羊毛狀微小孢子菌 Microsporum audouini 105 總狀毛黴菌 Mucor racemosus 106 疣孢漆斑菌 Myrothecixim verrucaria 107 黴白黴菌 Mucor mucedo 108 渺小白黴菌 Mucor pusillus 109 刺白黴菌 Mucor spinescens 100 魯氏白黴菌 Mucor rouxii 111 紅麵菌 Monascus ruber 112 鵝口瘡菌 Monilia Candida 113 仁果叢梗孢菌 Monilia fructigena 114 黑色叢梗孢菌 Monilia nigral 115 桃褐腐叢梗孢菌 Monilia laxa 116 刺黑烏黴菌 Menoniella echinita 117 紅麵包黴菌 Neurospora crassa 118 稻褐紋病菌 Nigrospora oryzae 119 好食脈孢菌 Neurospora sitophila 120 球黑孢黴菌 Nigrospora sphaerica 121 Ocuremonium charticola 122 頻繁青黴 Penicillium frequentance 152257.doc -11 - 201138627 123 橘青黴 Penicillium citrinum 124 變幻青黴 Penicillium variabile 125 產紫青黴 Penicillium purpurogenum 126 藍色青黴 Penicillium glaucum 127 支鏈澱粉黴 Pullularia pullulans 128 藍酪黴 Penicillium roquerforiti 129 淡黃青黴 Penicillium luteum 130 擴展青黴 Penicillium expansum 131 魚肝油青黴 Penicillium piscarium 132 皺褶青黴 Penicillium rugulosum 133 圓弧青黴 Penicillium cyclopium 134 產黃青黴 Penicillium chrysosgenum 135 黃綠青黴 Penicillium citreo-viride 136 點青黴 Penicillium notatum 137 紅色青黴 Penicillium rubrum 138 草酸青擻 Penicillium oxalicum 139 繩狀青徽 Penicillium funiculosum 140 柑橘綠黴 Penicillium digitatum [表3] 真 141 島青黴 Penicillium islandicum 菌 142 黑青黴 Penicillium nigricans 類 143 淡紫青黴 Penicillium lilacinum 144 微紫青黴 Penicillium spinulosum 145 煙色盤多毛孢 Pestalotia adusta 146 疏忽盤多毛孢 Pestalotia neglecta 147 柑桔擬莖點黴 Phomosis citri 148 歧皺青黴 Penicillium steckii 149 柑桔莖點黴 Phoma citricarpa 150 土壤莖點黴 Phoma terrestius 151 頭狀莖點黴 Phoma glomerata 152 冬莖點黴 Phoma pigmentivora 153 膜醭畢赤酵母菌 Pichia membranaefaciens 154 睞球菌 Peptococcus sp. 155 奇異變形桿菌 Proteus mirabilis 156 Phacidipycnus funfuracea 157 福士擬莖點黴 Phomopsis fukushii 158 德巴利腐黴 Pythium debaryanum 159 畸雌腐擻 Pythium irregulare 152257.doc -12- 201138627 160 瓜果腐黴 Pythium aphanidermatam 161 茄紋擬莖點黴 Phomopsis vexan 162 大雄疫黴 Phytophthora megasperma 163 煙草疫黴 Phytophthora nicotianae 164 馬鈴薯晚疫黴 Phytophthora infestans 165 台灣番椒疫黴 Phytophthora capsici 166 十字花科根瘤菌 Plasmodiophora brassicae 167 木栓化根腐菌 Pyrenochaeta licopersici 168 小紅酵母菌 Rhodotorula mimuta 169 膠紅酵母菌 Rhodotorula mucilaginosa 170 德克薩斯酵母菌 Rhodotorula texensis 171 黏紅酵母菌 Rhodotorula glutinis 172 Rhodotorula gulinis 173 乳糖酵母菌 Rhodotorula lactosa 174 黑根徽 Rhizopus nigricans 175 米根黴 Rhizopus oryzae 176 匍枝根黴 Rhizopus storonifer 177 代氏根黴 Rhizopus delemar 178 馬龄菩根徽 Rhizopus solani 179 爪哇根黴 Rhizopus javanicus 180 申克氏孢絲菌 Sporotrichum shenki 181 桿形裂絲藻 Stichococcus bacillavis 182 苗核病致病菌 Sclerotina fructincola 183 巴氏類酵母~~' Saccharomycodes pasteurianus 184 穗黴菌 Stachybotrys sp. 185 紫穗黴 ^ Spicaria vlolacea 186 縊縮齒梗孢 ' Scolecobasidium constrictum 187 尖端賽多孢~~ Scedosporium apiospermum 188 總狀共頭黴" Syncephalastrum racemosum 189 葡萄穗黴—' Stachybotrys chartarum 190 申克氏孢絲菌 ' Sporothrix schenckii 191 洋蔥白腐病 Sclerotium cepivorum 192 律草早絲殼菌 Sphaerotheca humuli 193 菌核病菌 Sclerotinia sclerotiorum 194 小帚樣徽菌" ~ Scopulariopsis brevicaulis 195 髮癖菌 " - Trichophyton mentagrophytes 196 石膏樣髮癬菌 Trichophyton gypseum 197 紅色髮癖菌 Trichophyton rubrum 198 粉紅單端孢 Trichothecium roseum 199 綠色木黴 Trichoderma viride 152257.doc •13- 201138627 200 埃澤樓髮癬菌 Trichophyton ajelloi 201 康寧木黴菌 Trichoderma koningii 202 木黴T-1 Trichoderma T-1 203 哈茨木黴 Trichoderma harzianum 204 白色球擬酵母 Tolulopsis Candida 205 皮狀絲孢酵母 Trichosporum cutaneum 206 木素木黴 Trichoderuma lignorum 207 黑細基格抱 Ulocladium atrum 208 玉蜀黍黑穗病菌 Ustilago zeae 209 黃萎輪枝孢菌 Verticillium albo-atrum 210 大理花輪枝孢菌 Verticillium dahliae 211 Wallemia sebi 212 瘤蓋乾酪菌 Tyromyces palustris 213 雲芝 Trametes versicolor 214 伏果乾腐菌 Serpula lacrymans [表4] 細 1 糞產鹼菌 Alcaligenes faecalis 菌 2 黏乳產鹼菌 Alcaligenes viscolactis 3 豌豆殼二孢 Ascophyta pisi 4 自營菌 Autotrophic bacteria 5 翠菊黃萎病病原菌 Aster yellows 6 醋酸妈不動桿菌 Acinetobacter calcoaceticus 7 Achrcmobacter gulyatus 8 產氣氣桿菌 Aerobacter aerogenes 9 陰溝氣桿菌 Aerobacter cloacae 10 義大利芽生菌 Blastomyces italicum 11 仙人掌桿菌 Bacillus cereus 12 蕈狀桿菌 Bacillus mycoides 13 枯草桿菌 Bacillus subtillis 14 巨大芽孢桿菌 Bacillus megaterrium 15 炭疽桿菌 Bacillus anthracis 16 Bacillus punctatum 17 Bacterium vulgar。 18 綠膿桿菌 Bacterium pyocyaneum 19 皮炎芽生菌 Blastomyces dermatidis 20 脆弱類桿菌 Bacterroid fragilis 21 胚胎彎曲桿菌 Campylobacter fetus 22 產氣莢膜梭菌 Clostridium perfringens -14- 152257.doc 201138627 23 難治梭孢桿菌 Clostridium difficile 24 地衣狀伏革菌 Corticium fuciforme 25 肉毒桿菌 Clostridium botulinum 26 克勒克檸檬形酵母菌 Cloeckera apiculata 27 結合纖維單胞菌 Cellulomonas iugis 28 曲狀桿菌 Campylobacter jejuni/coli 29 樹狀指孢黴 Dactylium dendroides 30 葡萄生色二孢 Diplodia viticol 31 漢遜德巴利酵母 Debaryamyces hansenii 32 去績狐菌 Desulfovibrio desulfuricans 33 栗疫菌 Endothia paracitica 34 大腸桿菌 Escherichia coli 35 產氣腸桿菌 Enterobacter aerogenes 36 陰溝腸桿菌 Enterobacter clocae 37 胡蘿蔔軟腐菌 Erwinia carotovora 38 核粒梭狀桿菌 Fusobacterium nucleatum 39 產氨黃桿菌 Flavobacterium aminogenes 40 黃質菌 Flavobacterium meningosepticum 41 葡萄糖酸桿菌 Gluconobacter suboxydans 42 漢遜酵母 Hansenula anomala 43 產酸克雷伯士菌 Klebsiella oxytoca 44 克雷白氏肺炎菌 Klebsiella pneumoniae 45 嗜酸乳桿菌 Lactbacillus acidophilus 46 胚芽乳桿菌 Lactbacillus planntarum 47 單增李斯特氏菌 Listeria monocytogens 48 嗜肺退伍軍人菌 Legionella pneamophila 49 鉤端螺旋體 Leptospira interrogans 50 冠狀環柄菇 Lepiota criststa 51 栗色環柄菇 Lepiota castanae 52 保加利亞桿菌 Lactobacillus bulgericus 53 麩胺酸微球菌 Micrococcus glatamicus 54 結核分枝桿菌 Mycobacterrium tuberculosis 55 白色微球菌 Micrococcus albus 56 Micrococcus aquilis 57 凝聚微球菌 Micrococcus conglomerates 58 變異微球菌 Micrococcus varians 59 淡紫擬青黴 Paecilomyces lilacinus 60 醬油片球菌 Podiococcus soyae 61 乳酸片球菌 Podiococcus acidilactici 62 銅綠假單胞菌 Pseudomonas aeruginosa 152257.doc -15- 201138627 63 螢光假單胞菌 Pseudomonas fluresceus 64 宛氏擬青黴 Paecilomyces variotii 65 紅發夫酵母 Phaffia rhodozyma 66 異常畢赤酵母 Pichia anomala 67 膜醭畢赤酵母 Pichia membranaefaciens 68 普通變形桿菌 Proteus vulgaris 69 範特腐黴 Pythium vanterpoolii 70 西瓜灰絨泡菌 Phyrasium cinereum 71 痤瘡丙酸桿菌 Propionibacterium aces 72 薛氏丙酸桿菌 Propionibacterium shermanii 73 蘋果白粉病菌 Podosphaera leucotricha 74 紫丁香假單胞菌 Pseudomonos syringae 75 青枯假單胞菌 Pseudomonos solanacearum [表5] 細 76 類產氣副大腸桿菌 Paracolabactrum aerogenoides 菌 77 紫色絲核菌 Rhizoctonia violacea 78 立枯絲核菌 Rhizoctonia solani 79 立克氏立克次體 Rickettsia rickettsii 80 瘤胃球菌 Ruminococcus 81 油菜菌核病菌 Scleotina scleotiorum 82 擲孢酵母 Sporobolomyces roseus 83 乳酸鏈球菌 Streptococcus lactis 84 粟酒裂殖酵母 Schizosaccharomyces pombe 85 路得類酵母 Saccharomycodes ludwigii 86 黏質沙雷氏桿菌 Serratia marcesens 87 金黃色葡萄球菌 Staphylococcus aureus 88 鼠傷寒沙門氏菌 Salmonella typhimurium 89 網狀鏈輪絲菌 Streptoverticillum reticulum 90 糞鏈球菌 Staphylococcus faecalis 91 腸炎沙門氏菌 Salmonella enteritidis 92 腸道沙門氏菌 Salmonella enterrica 93 亞利桑那沙門氏菌 Salmonella arizonae 94 副傷寒沙門氏菌 Salmonella paratyphi 95 豬霍亂沙門氏菌 Salmonella choleraesuis 96 無乳鏈球菌 Streptococcus agalactiae 97 Serratia marcesceus 98 液化沙雷氏菌 Serratia liguefaciens 99 釀酒酵母 Saccharomyces cerevisiae 152257.doc -16- 201138627 100 Sugeran mosaic 101 上皮葡萄球菌 Staphylococcus epidermidis 102 人葡萄球菌 Staphylococcus hominis 103 無乳鏈球菌 Staphylococcus agalactiae 104 金黃色i萄球菌 Staphylococcus pneumoniae 105 酿腹葡萄球菌 Staphylococcus pyogenes 106 嗜鹽沙雷菌 Serratia salinaria 107 傷寒沙門氏菌 Salmonella typhosa 108 黃色八疊菌 Sarcina flava 109 卵黃八疊菌 Sarcina latea 100 黏球生孢噬纖維菌 Sporocytohaga myxococcoides 111 黑色圓酵母 Torula nigra 112 普通高溫放線菌 Thermoactinomyces vulgaris 113 嗜酸硫桿菌 Thiobacillus asidophilus 114 柔軟硫桿菌 Thiobacillus delicatus 115 脫氮硫桿菌 Thiobacillus denitrificans 116 氧化亞鐵硫桿菌 Thiobacillus ferrooxidans 117 中間硫桿菌 Thiobacillus intermedius 118 Thiobacillus kabolis 119 那不勒斯硫桿菌 Thiobacillus neapolitans 120 新型硫桿菌 Thiobacillus novellus 121 代謝不完全硫桿菌 Thiobacillus perometabolis 122 粉色硫桿菌 Thiobacillus rubellus 123 氧化硫硫桿菌 Thiobacillus thiooxidans 124 排硫桿菌 Thiobacillus thioparus 125 依氏嗜熱硫桿菌 Thiobacillus thermophilica imschenetskii 126 多能硫桿菌 Thiobacillus versutus 127 創傷孤菌 Vibrio ulnificus 128 蘋果黑星病菌 Venturia inaequalis 129 耶辛尼氏腸炎桿菌 Yersinia enterocolitica 130 白喉棒桿菌 corynebacterium diphtheriae 131 麩胺酸棒桿菌 corynebacterium glutamicum 又’本發明之組合物對例如源自植物之過敏原,源自黴 菌之過敏原,蟎蟲、蟑螂或者排泄物等之動植物蛋白質等 過敏原發揮出抗過敏性。 進而,本發明之組合物對例如美洲室塵蟎、歐洲室塵蟎 等塵蟎類,河野脂蟎、長毛粉蟎、橢圓食粉蟎等粉蟎類, 152257.doc -17· 201138627 南爪蜗、馬六甲肉食蜗、強壯肉食瞒、普通肉食蝶、鱗翅觸 足蜗等肉食蜗類’柏氏禽_、林禽偶、雞皮刺蜗、故皮 刺蜗等禽類,球腹㈣類,㈣類等發揮出防蜗蟲性、。 其次’對本發明之抗菌性處理劑及抗菌性成形品進行説 (抗菌性處理劑及抗菌性成形品) 本發明之抗菌性處理劑含有本發明之組合物與分散介 質’例如可列舉:生活用喷霧劑、塗料、塗布劑、表面處 理劑、及纖維處理劑等。 作為分散介質,例如可列舉:水、甲醇、 等低級醇’聚乙二醇、聚乙稀醇等。又,為了容易地將: 發明之組合物固定於纖維製品等被黏附體上 菌性處賴巾混合黏合樹脂。 丙稀酸系樹脂、聚胺基甲 乙烯-乙酸乙烯酯共聚樹 作為黏合樹脂’例如可列舉: 酸酯、聚矽氧烷、聚氣乙烯、氣 脂等。 与r徒南耐久性,較佳為本發明之抗菌性處理劑令 :交聯劑。作為交聯劑,可列舉:氮…封端異氣酿 s曰、水分散異氰酸酯、三聚氰胺、水性環氧化合物、碳二 醯亞胺等。 抗菌性處理劑例如可藉由將本發明之組合物、分散介質 及黏。劑搗碎混合而獲得。χ,亦可將本發明之組合物分 散至丙埽g夂系樹脂之單體或苯乙烯單體、或該等之混合物 ;5清形時’係於塗布抗菌性處理劑後,照射紫外線 I52257.doc 201138627 或加熱使單體聚合,使之於成形品上硬化。 . 本發明之杬菌性成形品係利用本發明之抗菌性處 1行處理者,例如可列舉:纖維、布帛等纖維製品, • “曰膜’將纖維或布帛積層於樹脂膜上而成的積層體等。 、、㈣用本發明之抗H性處理劑處理該等纖維製品等的 厂^例如可列舉:將被黏附體或作為該等之原材料的材 厂5 j准次凊於含有本發明之組合物的液狀纖維處理劑中 的^法等。作為浸潰方法,可列舉所謂凹槽浸潰等。又, 、°采用利用喷霧劑等對被黏附體之表面進行喷霧的方 法。 南利用作為本發明之抗菌性處理劑之一例之塗料、塗布 劑、表面處理劑的方法,可列舉:刷塗或輥塗、藉由喷墨 或凸版等之印刷、散佈、刮塗或喷塗、凹板印刷式塗、淋 塗模塗、到刀式塗布等各種塗布手段;或者網版印刷、 移印、套版印刷、喷墨印刷等各種印刷手段等。 利用本發明之抗菌性處理劑進行處理之纖維製品,例如 可列舉.棉、|月、羊毛等天然纖維,聚醋 '尼龍、丙稀猜 #合成纖維、半合成纖維、再生纖維等短纖維或長纖維, 可為使用該等纖維之2種以上的複合纖維’亦可為織物、 編織物、不織布等布帛。 作為樹脂膜,例如可列舉:PVC(聚氣乙稀)或TP0(稀煙 系彈性體)或PU(聚胺基甲酸酯)、聚酯等之膜。又,作為 本發明之抗菌性成形品,可列舉:於上述膜上設置布帛之 合成皮革、人工皮革、防水布等樹脂膜積層體。 152257.doc -19· 201138627 本發月之抗菌性成形品含有本發明之組合物與樹 脂,亦可為將其成形而成者。 作為樹脂,例如可列舉:成形用樹脂、纖維用樹脂、橡 膠狀樹脂等。 並且,可將本發明之組合物與樹脂之混合物熔融藉由 拉伸為纖維狀或進行擠出成形之公知成形方法,將其製成 纖維或膜,而獲得本發明之抗菌性成形品。又,亦可製成 含有纖維之布帛等纖維製品、或將膜積層而成之樹脂膜積 層體,而獲得本發明之抗菌性成形品。 作為本發明之抗菌性處理劑之一例,例如可列舉:作為 家用或產業用材料之内外裝塗料、家用或車輛内裝用之喷 霧劑、地毯清潔劑、膜或片材用之塗布劑或表面處理劑、 纖維積層用之接著劑、砂t、水泥、壁材用之粉刷等。 又,作為利用本發明之抗菌性處理劑進行處理之被黏 體,可列舉:利用纖維積層用之接著劑進行加工之人工 革、含有氣乙烯、紙及布$中之至少—種的壁紙、建材 木材、地板材、傢倶用及建裝材用之化粧合板、鋁窗格 建築用鋁板等鋁材、樹脂成形材、洗浴用品、飼料容器 構成空調裝置之空調風路的空調風路構件、鋼鐵製品、 用毯子、屋頂材、隔熱材、廚房用品、盥洗室用品室 用品、寢具類、過濾器類、傢倶類、紙製 〇 ^ 杌具、皮 σο寻 〇 (實施形態之效果) 本發明之組合物由於含有2種咪唑系 〜另躅系抗菌劑 152257.doc -20- 201138627 與抗過敏劑’故而藉由抑制作為過敏誘發物質之成因之 菌、黴菌、蟎蟲之產生,可使抗過敏劑之含量為少量,而 發揮實用之過敏誘發物質之去活化性能。 尤其是’藉由將2種咪唑系之有機系抗菌劑設為具有苯 并咪唑環及噻唑基之化合物、與具有苯并咪唑環及胺基甲 酸酯基之化合物,可製成抗菌性、抗黴菌性更優異之組合 物0 並且,本發明之組合物由於進而含有無機系抗菌劑,故 而可進一步提高抗菌性、防黴菌性。 尤其疋,藉由將無機系抗菌劑設為載銀碟酸錄,可獲得 抗菌作用之相乘效果,製成發揮出更加顯著之抗菌、防黴 菌性之組合物。 又,本發明之組合物由於進而含有除蟎蟲劑,故而防蟎 蟲性進一步提高。 尤其疋’藉由將除蟎蟲劑設為氧化硼或含有其之玻璃 質,可使含有該組合物之抗菌性成形品變得不易發生由 光、熱引起之變色》 又,本發明之抗菌性處理劑含有本發明之組合物、與分 散介質,尤其為生活用喷霧劑、塗料、塗布劑、表面處理 劑、及纖維處理劑等。因此,變得容易將組合物塗布於被 黏附體上,可製成便利性優異之抗菌性處理劑。 又,本發明之抗菌性處理劑由於含有黏合樹脂,故而可 有效地使組合物固著在被黏附體上。 此外,藉由併用交聯劑,可提高固著耐久性。即,即使 152257.doc 21 201138627 反覆進行洗務,亦可長時間維持抗菌性、防徽菌性、防瞒 蟲性、抗過敏性。 並且,本發明之抗菌性成形品由於係利用本發明之抗菌 性處理劑對纖維、布帛、樹脂膜、將纖維或布帛積層於樹 脂膜上而成之積層體中之任—者進行處理而成者,故而應 用範圍廣,便利性優異。 又,本發明之抗菌性處理劑由於抗過敏劑之含量相對較 少,故而經抗菌性處理劑處理之抗菌性成形品之質地良 好,不易發生由光、熱引起之變色。因此,綜合而言可獲 得清潔之空間。 又本發明之抗菌性成形品含有本發明之組合物與樹 脂,亦可為將其成形而成者。本發明之組合物由於抗過敏 劑之含量較少’故而可製成質地良好,不易發生由光、熱 引起之變色的抗菌性成形品。 [實施例] 以下,列舉實施例及比較例等,更加具體地說明本發 明’但本發明並不限定於實施例等之内容。 [實施例1 -1至4-2及比較例1 _ 1至5] (抗菌性處理劑及抗菌性成形品之製造) 實施例1-1至4-2及比較例1_1至5係藉由如下方式實施。 (實施例1-1) 實施例1-1中’於下述製造例U中製備水系噴霧劑,於 下述製造例1-2中使用製造例1_1之水系喷霧劑加工濾紙, 藉此製作加工濾紙。 I52257.doc •22· 201138627 (製造例1-1) 將表6之(1A)至(3 A)於燒杯中攪拌混合,利用蒸餾水 (4A)稀釋至 1 L 之容積。利用 LabStar LMZ06(Ashizawa Finetech股份有限公司製造)並使用直徑為0.5 mm之氧化結 珠,將混合液搗碎混合20分鐘。此時,以液體黏度成為 700 mPa*s至800 mPa*s之方式隨時添加三仙膠進行製備, 而製成作為抗菌性處理劑之水系喷霧劑。 [表6] (1A) 抗菌性組合物 2-(4-噻唑基)-1Η-苯并咪唑(35質量%)、1H-2-苯并咪唑胺基甲酸曱酯(35質量%)、及載銀 磷酸锆(30質量%)之混合物 3 g (2A) 抗過敏劑 聚乙稀盼 (平均分子量:3,000) 4.5 g (3A) 分散劑 Noigen TDS-100 (第一工業製藥股份有限公司) 3g (4A) 蒸餾水 - 936 g (製造例1-2) 使用家用喷霧器,以塗布量成為50 g/m2之方式對濾紙 (八0乂八]^丁£(:股份有限公司製造,:^〇.2)噴霧製造例1-1之 水系喷霧劑,而製作加工濾紙。使用該加工濾紙,實施下 述抗菌性試驗等。 (實施例1-2) 實施例1-2中,除將濾紙變更為聚酯編織物(Tricot布料 基重為320 g/m2)以外,與實施例1-1同樣地製作加工織 物。使用該加工布$,實施下述抗菌性試驗等。 (實施例2-1) 152257.doc •23· 201138627 實施例2-1中’於下述製造例2-1中製備纖維處理劑,於 下述製造例2-2中使用製造例2-1之纖維處理劑加工布料, 藉此製作加工布帛,並實施下述抗菌性試驗等。 (製造例2_1) 將表7之(1B)至(3B)於燒杯中合併混合後,利用上述 LabStar LMZ06並使用直徑為〇.5 mm之氧化锆珠磨碎混合 3 0分鐘,而製備纖維處理劑。 [表7] (1B) 抗菌性組合物 2-(4-噻唑基)-iH-苯并咪〇坐(50質量%)與1H-2-苯并咪唑胺基曱酸甲酯(50質量%)之混合物 180 g (2B) 抗過敏劑 Polyphenon 70A (三井農林股份有限公司) 20 g (3B) 黏合樹脂 Light Epoch AX-30 (Hokko Chemical股份有限公司) 300 g (製造例2-2) 利用蒸餾水將製造例2- 1之纖維處理劑稀釋為20倍之容 量,於金屬捅内將尺寸為A4之布料於含有纖維處理劑之溶 液中浸潰5秒鐘。此處,布料係使用標準棉布之密織棉布3 號。繼而,利用輥間壓力為4.0 kg/cm2之碾壓機進行擠壓 (擠壓率:100%),利用熱風乾燥機於120°C之溫度下乾燥 10分鐘,而製作實施例2-1之加工布帛。 (實施例2-2) 實施例2-2中,於製造例2-1中製備纖維處理劑,於下述 製造例2-3中使用製造例2-1之纖維處理劑加工布料,藉此 製作加工布帛,並實施下述抗菌性試驗等。 152257.doc •24_ 201138627 (製造例2-3) 利用瘵餾水將製造例2- 1之纖維處理劑稀釋為丨〇倍之容 量,於金屬桶内將尺寸為Α4之布料浸潰於含有纖維處理劑 之溶液中5秒鐘。此處,布料係使用尼絲紡(Nyl〇n, 基重為110 g/m2)。繼而,利用輥間壓力為4 〇 kg/m2之碾壓 機進行擠壓(擠壓率:5〇%),利用熱風乾燥機於i2〇<>c之溫 度下乾燥2分鐘,於150〇c下熱處理丨分鐘,藉此製作實施 例2-2之加工布帛。 (實施例2-3) 實施例2-3中,於製造例2 —丨中製備纖維處理劑,於下述 製造例2-4中使用製造例2_丨之纖維處理劑加工布料,藉此 製作加工布帛,並實施下述抗菌性試驗等。 (製造例2-4) 利用瘵餾水將製造例2-1之纖維處理劑稀釋為15倍之容 量’於金屬桶内將尺寸為A4之布料浸潰於含有纖維處理劑 之溶液中5秒鐘。此處,布料係使用聚酯/棉混(65〇/。/35%) 平紋2组織物(基重為120 g/m2)。繼而’利用輥間壓力為4 〇 kg/m2之碾壓機進行擠壓(擠壓率:7〇%)’利用 於贿之溫度下乾燥3分鐘,於峨下熱處理 此製作實施例2-3之加工布帛。 (實施例3-1) 實施例3-丨中,於下述製造例3_丨中製備表面處理劑,於 下述製造例3-2中製備纖維處理劑。並且,於製造例μ中 使用製造例3奴表面處理劑及製造例3_2之纖維處理劑加 152257.doc •25· 201138627 工合成皮革,藉此製作加工合成皮革。 (製造例3-1) 將表8之(1C)及(2C)以粉末狀態充分混合,將該混合物 添加至(3C)中,利用AGI Homomixer(Primix股份有限公司 製造,T. K. Robomix)攪拌混合約5分鐘,製備作為合成皮 革用之抗菌性處理劑之表面處理劑。 [表8] (1C) 抗菌性組合物 2-(4-噻唑基)-1Η-苯并咪唑(35質量%)、1H-2-苯并咪唑胺基曱酸甲酯(35質量%)、及載 銀雄酸錯(30質量%)之混合物 0.025 g (2C) 抗過敏劑 磷酸锆(70質量%)與單寧酸(30質量%)之混 合物 1.0 g (3C) 處理劑樹脂 Leatheroid LU-4305SP(大日精化工業股份 有限公司) 100 g (製造例3-2) 利用上述LabStar LMZ06並使用直徑為0.5 mm之氧化鍅 珠,將利用(3D)之蒸餾水稀釋表9之(1D)及(2D)而成之混合 液捣碎混合20分鐘’製備合成皮革用之纖維處理劑。 [表9] (ID) 防蟎蟲劑 含有氧化硼(10質量%) 之玻璃粉末 20 g (2D) 黏合樹脂 Evafanol AS-21 (曰華化學股份有限公司) 200 g (3D) 蒸餾水 - 780 g (製造例3-3) 首先,於尺寸為20x20 cm之合成皮革之背面(基布側), 均勻喷霧製造例3-2之纖維處理劑2 g,利用熱風乾燥機於 152257.doc -26 - 201138627 110 C之溫度下乾燥5分鐘。繼而,利用棒式塗布機,於表 面(銀面側)塗布製造例3_丨之表面處理劑4 g’再次於ii〇<t 之溫度下乾燥5分鐘。藉此,製作作為實施例%〗之抗菌性 成形品之加工合成皮革》合成皮革係使用銀面由聚胺基甲 酸S曰製造且基布為PET(聚對笨二曱酸乙二酯)丨〇〇%編布帛 者。 (實施例3-2) 貫施例3-2中’於製造例3-1中製備表面處理劑,於下述 製造例3 -2中製備纖維處理劑。於製造例3_4中使用製造例 3-1之表面處理劑及製造例3-2之纖維處理劑加工合成皮 革,藉此製作加工合成皮革。 (製造例3-4) 首先,利用凹板輥,於尺寸為20x20 cm之合成皮革之背 面(基布側)塗布製造例3-2之纖維處理劑2 g,利用熱風乾 燥機於110°C之溫度下乾燥5分鐘。繼而,利用棒式塗布 機,於表面(銀面側)塗布製造例3-1之表面處理劑4 g,再 次於110°C之溫度下乾燥5分鐘。藉此,製作作為實施例3_ 2之抗菌性成形品之加工合成皮革。合成皮革係使用銀面 由聚胺基曱酸酯製造且基布為尼龍100%編織物者。 (實施例4-1) 實施例4-1中,於下述製造例4-1中製備纖維處理劑,於 下述製造例4-2中使用製造例4-1之纖維處理劑加工布料, 藉此製作加工布帛。 (製造例4-1) 152257.doc •27· 201138627 將利用蒸餾水(4E)稀釋表10之(1E)至(3E)而成之混合液 於燒杯中合併攪拌後,利用上述LabStar LMZ06並使用直 徑為0.5 mm之氧化锆珠搗碎混合30分鐘,製備作為抗菌性 處理劑之纖維處理劑。 [表 10] (1E) 抗菌性組合物 2-(4-噻唑基)-1Η-苯并咪唑(35質量%)、 1H-2-苯并咪唑胺基曱酸甲酯(35質量 %)、及載銀磷酸鍅(30質量%)之混合物 60 g (2E) 抗過敏劑 氧化鍅 75 g (3E) 分散劑 Noigen TDS-100 (第一工業製藥股份有限公司) 60 g (4E) 蒸餾水 - 855 g (製造例4-2) 將製造例4-1之纖維處理劑(35 g)、曰華化學股份有限公 司製造之Neostecker SI(10 g)及蒸餾水455 g混合,於金屬 桶内將尺寸為A4之布料浸潰於含有纖維處理劑之溶液中1 0 秒鐘。此處,布料係使用基重為270 g/m2之PET 100% Tricot布料。 繼而,利用輥間壓力為4.0 kg/cm2之碾壓機進行擠壓(擠 壓率:95%),利用熱風乾燥機於120°C之溫度下乾燥10分 鐘。藉此,製作作為實施例4-1之抗菌性成形品之加工布 帛。 (實施例4-2) 實施例4-2中,於製造例4-1中製備纖維處理劑,於下述 製造例4-3中使用製造例4-1之纖維處理劑加工布料,藉此 製作加工布帛。 152257.doc -28- 201138627 (製造例4-3) 將製造例4-1之纖維處理劑(35 g)、日華化學股份有限公 司製造之Neostecker SI(10 g)、曰華化學股份有限公司製 造之*反一酿亞胺系交聯劑NK Assist Cl 1 0 g(交聯劑)及蒸 顧水445 g混合,於金屬桶内將尺寸為A4之布料浸潰於含 有纖維處理劑之溶液中1 〇秒鐘。此處,布料係使用基重為 270 g/m2之PET 100% Tricot布料。繼而,利用輥間壓力為 4.0 kg/cm之礙壓機進行擠壓(擠壓率:95%),利用熱風乾 燥機於120C之溫度下乾燥1〇分鐘。藉此,製作作為實施 例4-2之抗菌性成形品之加工布帛。 (比較例1 -1) 比較例1-1中,準備與實施例U所使用之濾紙相同且未 經喷霧加工者。 (比較例1-2) 比較例1-2中,準備與實施例1-2所使用之聚醋編織物相 同且未經噴霧加工者。 (比較例2-1) 比較例2-1中,於下述製造例5-1中製備纖維處理劑,於 下述製造例5-2中使用製造例5-丨之纖維處理劑加工布料, 藉此製作加工布寒。 ·、 (製造例5-1) 將表11之(1F)至(3F)於燒杯中合併攪拌後,利用上述 LabStar LMZ06並使用直徑為〇 5顏之氧化錐珠搗碎混二 3〇分鐘,製備纖維處理劑。 σ 152257.doc -29- 201138627 [表Η] (IF) 抗菌性組合物 吡啶硫酮鋅 1 OA (2F) 抗過敏劑 Polyphenon 70A -- 20 g (三井農林股份有限公司、 (3F) 黏合樹脂 Light Epoch AX-30 300 g (Hokko Chemical股份有限公司) (製造例5-2) 利用蒸餾水將製造例5-1之纖維處理劑稀釋為2〇倍之容 1,於金屬桶内將尺寸為A4之布料於含有纖維處理劑之溶 液中浸潰5秒鐘。此處,布料係使用標準棉布之密織棉布3 號。 " 繼而,利用輥間壓力為4.0 kg/cm2之碾壓機進行擠壓(擠 壓率:1〇〇%),利用熱風乾燥機於12(rc之溫度下乾燥分 鐘,製作比較例2-1之加工布第。 (比較例2-2) 比較例2-2中’於製造例中製備纖維處理劑,於製造 例5-3中使用製造例w之纖維處理劑加工布料,藉此製作 加工布帛’並實施下述抗菌性試驗等。 (製造例5-3) 利用蒸館水將製造例5 _ 1之纖維處理劑稀釋為i 〇倍之容 量,於金制㈣尺寸為A4之布料於含有纖維處理劑之溶 液中浸潰5秒鐘。此處,布料係使用尼絲紡。 繼而,利用輥間壓力為4.〇 kg/cm2之艰壓機進行擠壓(擠 壓率:50%)’利用熱風乾燥機於12()t 鐘’於⑽下熱處理i分鐘,藉此製作比較例二: 152257.doc -30- 201138627 布帛。 (比較例2-3) 比較例2-3中,於製造例5_丨中製備纖維處理劑,於製造 例5·4中使用製造例5_丨之纖維處理劑加工布料,藉此製作 加工布帛。 ' (製造例5-4) 利用蒸餾水將製造例5-1之纖維處理劑稀釋為15倍之容 量’於金屬桶内將尺寸為A4之布料於含有纖維處理劑之溶 液中浸潰5秒鐘。此處,布料係使用聚酯/棉混(65%/35%) 平紋組織物(基重120 g/m2)。繼而,利用輥間壓力為4 〇 kg/m2之礙壓機進行擠壓(擠壓率:7〇%),利用熱風乾燥機 於120°C之溫度下乾燥3分鐘,於ISOt下熱處理丨分鐘,藉 此製作比較例2-3之加工布帛》 (比較例3) 比較例3係於實施例3-1之製造例3-3中不於合成皮革之 背面噴霧纖維處理劑,另外塗布Leatheroid LU-4305SP(大 曰精化工業股份有限公司製造)4 g代替製造例^丨之表面處 理劑,除此以外’於與實施例3-1相同之條件下製作不含 抗菌性組合物、抗過敏劑、防蟎蟲劑的比較例3之未加工 ' 合成皮革。 (比較例4) 比較例4係於實施例4-1之製造例4-1中將表1〇之(4£)笑館 水增加至930 g,而不使用表10之(2E)氧化鍅(75 以外’於與製造例4-1相同之條件下製備纖維處理 扣J 0繼 152257.doc -31· 201138627 而,將所製備之纖維處理劑(35 g)、日華化學股份有限公 司製造之Neostecker SI(10 g)混合,用作含有纖維處理劑 之溶液’除此以外,於與製造例4_2相同之條件下製作加 工布帛。 (比較例5) 比較例5中’準備與實施例4_ 1所使用之PET 100% Tricot 布料相同且未經加工者。 其次’對實施例及比較例之成形品實施抗菌性試驗 '防 黴菌試驗、蟎蟲抑制試驗及抗過敏原試驗。 (抗菌性試驗) 對實施例2-1至2-3、4-1、4-2及比較例2-1至2-3、5之布 帛實施抗菌性試驗。 抗菌性試驗係依據JIS_L_ 1902(2002年)菌液吸收法而實 施。菌種係使用黃色葡萄球菌與肺炎桿菌此兩種,於實施 例2-1至2-3、4-1、4-2及比較例.2-1至2-3、5之布帛與棉標 準白布上接種菌液,使用下述式(數丨)算出殺菌活性值;將 其結果示於表12。 殺菌活性值=Log(a/b)…(數1) a :剛接種棉標準白布後之菌數 b :布帛培養18小時後之菌數。 152257.doc -32· 201138627 [表 12] 試料 殺菌活* 1±值 黃色葡萄球菌 肺炎桿菌 實施例2-1 L. 加工布料(密織棉布3號) >1.5 1.4 實施例2-2 加工布料(尼龍) >1.5 1.3 實施例2-3 加工布料(聚酯/棉) >1.5 1.4 比較例2-1 利用其他抗菌劑之加工布料(密織棉布3號) >1.5 1.2 比較例2-2 利用其他抗菌劑之加工布料(尼龍) >1.5 1.2 比較例2-3 利用其他抗菌劑之加工布料(聚酯/棉) >1.5 1.1 實施例4-1 加工布料(PET Tricot) 1.2 >1.5 實施例4·2 加工布料(PET Tricot) 1.3 >1.5 比較例5 未加工布料(PET Tricot) -1.0 -0.8 若將實施例2-1至2-3、4-1、4-2與比較例2-1至2-3、5進 行比較’則得知:實施例2-1至2-3、4-1、4-2由於含有2-(4-°塞唾基)-1H-苯并啼吐及1H-2-苯并咪。坐胺基曱酸曱酯, 故而獲得抗菌性優異之加工布第。另一方面得知,比較例 5由於不含本發明之抗菌性組合物,故而不具有抗菌性。 又’比較例2-1至2-3由於含有本申請案以外之一般抗菌 劑,故而確認具有抗菌性》 (防黴菌性能試驗) 對貫施例 1-1、1-2、2-1至 2-3、3-1、3-2、4-1、4-2與比 較例1-1、1-2、2-1至2-3、3之濾紙、合成皮革、布帛實施 防黴菌性能試驗。 實施例1 -1之爐、紙係使用利用所製備之水系喷霧劑進行 喷霧後,於室溫下放置1小時者。自遽紙之中央部切取3 cmx3 cm見方,將喷霧面作為正面,進行下述20菌法防黴 菌性能試驗。又,未噴霧水系嘴霧劑之比較例1-1之渡紙 亦同樣地切取3 cm><3 cm見方’進行下述2〇菌法防黴菌性 152257.doc -33- 201138627 能試驗。 針對實施例3-1、3-2及比較例3之合成皮革,切取3 cmx3 cm見方,將銀面作為正面,進行下述20菌法防黴菌 性能試驗。 針對實施例1-2、2-1至2-3、4-1、4-2及比較例ι·2、2-1 至2-3之加工布帛,亦切取3 cm><3 cm見方,進行下述20菌 法防黴菌性能試驗。 於防黴菌性能試驗中,使用表14所示之試驗菌,依據下 述試驗方法及判定基準’確認實施例1 _ 1、1 _2、2-1至2-3、3 -1、3-2、4-1、4-2與比較例 1 -1、1 -2、2-1 至 2-3、3之 防黴菌性。 (防黴菌性能試驗方法) (培養基之製備) (1)防黴菌性能試驗所使用之培養基係採用於JI;S規格培 養基中添加馬铃薯葡萄糖培養液(Potato Dextrose Broth, Difco股份有限公司製造)的平板培養基,組成為下述表13 所示。將其於121°C下加熱蒸氣滅菌處理2〇分鐘。 (培養基之組成) [表 13] 1.000 ml 3-0 g 10 g 0-5 g 0.25g 0.002 g 7.0 g 25 g 純化水 硝酸銨 磷酸二氫鉀 硝酸鎂七水合物 氣化鉀 硫酸鐵(II)七水合物 馬鈴薯葡萄糖培養液(Difco公司製造) 瓊脂 152257.doc -34 201138627 (試驗菌液之製備) (2)於(1)所製備之培養基中接種表14之試驗菌,並充分培 養。於培養皿中添加下述表1 5之組合物之濕潤液20 ml, 回收孢子。將孢子液過濾後,將孢子數製備為lxl06±1個/ ' mL。孢子濃度較高時,利用自上述JIS規格培養基中除去 瓊脂而獲得的組成液進行稀釋。 (試驗菌之種類) [表 14] 1 鏈格孢菌 2 黑麴菌 3 雜色麴菌 4 土麴菌 5 褚麵菌 6 出芽短梗黴 7 球毛殼菌 8 芽枝狀枝孢菌 9 球孢枝孢菌 10 甄氏外瓶黴 11 腐皮鐮孢菌 12 黏帚黴菌 13 疲抱漆斑菌 14 稻褐紋病菌 15 宛氏擬青黴 16 橘青黴 17 繩狀青黴 18 紫附球菌 19 小帚樣黴菌 20 綠色木黴 (濕潤液之組成) [表 15] 純化水 l,000ml 磺基琥珀酸二辛酯鈉 0.05 g 152257.doc -35· 201138627 (培養) · 於(1)所製備之培養基上接種(2)所製備之孢子液後,在 其上分別承載實施例1-1及比較例1-1之濾紙、實施例3-1、 3-2及比較例3之合成皮革、實施例1-2、2-1至2-3、4-1、4-2及比較例1-2、2-1至2-3之加工布帛後,利用附帶濕度溫 度控制器之循環器,於溫度維持於29±1°C、濕度維持於 85%R · Η以上之狀態下培養28天。並且,每週(於培養開 始後第1週、第2週、第3週、第4週確認)目測確認黴菌之 繁殖狀況,根據下述表16所示之5個評價等級進行評價。 將其結果示於表17。 [表 16] 評價 試料表面之細菌生長 0 細菌完全未生長 1 10%以下生長 2 10〜30%以下生長 3 30~60%以下生長 4 60%以上完全生長 [表 17] 試料 1週後 2週後 3週後 4週後 實施例1-1 加工滤紙 0 0 0 0〜1 實施例1-2 加工布料 0 0 0 0 比較例1-1 加工渡紙 2 3 4 4 比較例1-2 加工布料 2 3 4 4 實施例2-1 加工布料 0 0 0 0 實施例2-2 0 0 0 0 實施例2-3 0 0 0 0 比較例2-1 其他抗菌劑加工布料 0 1 3 3 比較例2-2 0 1 3 3 比較例2-3 0 1 3 3 -36- 152257.doc 201138627 試料 1週後 2週後 3週後二 4调德 實施例3-1 加工合成皮革 0 〇 1 Λ 實施例3-2 加工合成皮革(凹版) 0 0 〇 U π 比較例3 未加工合成皮革 1 2 3 U Ί 實施例4-1 加工布料 —0 0 0 J Λ 實施例4-2 0 0 0 U 0 右將貫施例1 -1 1-2、2-1 至 2-3、3-1 3_2、4-1、4-2與 比較例M、i-2、W至2_3、3進行比較,則得知:各實施 例可獲得具有優異之防黴菌性的濾紙、合成皮革、布帛。 另一方面得知,各比較例由於不含有本發明之抗菌性組合 物’故而不具有防黴菌性。 (蜗蟲抑制試驗) 1-2、3-1、3-2、4-1、4_2及比較例卜 對實施例1-1 i-2、3、5之濾紙、合成皮革、布帛實施蟎蟲抑制試驗。 依據JIS_L_1920增殖抑制試驗a法,實施蟎蟲試驗例丨至 3作為瞒蟲抑制試驗。具體而言,蜗蟲係使用歐洲室塵蜗 (東京女子大學系)。將切成直徑為4⑽之實施例及比較例 之渡紙、合成皮革、布㈣設於培養皿上,於其上播種含 有7〇±1〇隻之蟎蟲培養基。其後,於25±2它、75±5% RH2 j境下進行培養,計數第4週及第6週之蟎蟲生存數,合計 實施3次,求出其合計生存數。由所求得之平均生存數及 下述式(數2)算出增殖抑制率。 增殖抑制率(%)=10〇x(c-d)/c…(數2) C:未加工成形品(濾紙、合成皮革、布帛)上之平均生存數 d .加工成形品(濾紙、合成皮革、布帛)上之平均生存數 (蜗蟲試驗例1) 152257.doc •37- 201138627 於蟎蟲試驗例1中,使用直徑為4 cm之實施例1 -1之加工 濾紙及比較例1-1之未喷霧之未加工濾紙作為試料,藉由 上述方式進行試驗。又,使用實施例1-2及比較例1-2之加 工合成皮革作為試料,將其切成直徑為4 cm之圓形並將基 布面朝上,藉由上述方式進行試驗。將6週後之結果示於 表18。 [表 18] 初期 生存蟎蟲數 6週後 生存蜗蟲數 增殖抑制率(%) 實施例1-1 225 2 >99.9 實施例1-2 3 >99.9 比較例1-1 6,977 • 比較例1-2 7,023 - (蟎蟲試驗例2) 於蟎蟲試驗例2中,使用實施例3-1、3-2之加工布帛及 比較例3之未加工合成皮革作為試料,將其切成直徑為4 cm之圓形並將基布面朝上,藉由上述方式進行試驗。將4 週及6週後之結果示於表19。 [表 19] 初期 生存蟎蟲數 4週後 生存蟎蟲數 增殖抑制率(%) 6週後 生存蟎蟲數 增殖抑制率(%) 實施例3-1 223 9 (99.8) 28 (99.7) 實施例3-2 8 (99.8) 27 (99.7) 比較例3 3,894 10,920 (蟎蟲試驗例3) 152257.doc -38 - 201138627 於瞒蟲試驗例3中’使用實施例4_ 1、4-2之加工布帛及 比較例5之未加工布帛作為試料’將其切成直徑為* cm之 圓形並藉由上述方式進行試驗。將4週及6週後之結果示於 表20。 [表 20] 初期 生存蟎蟲數 4週後 生存蟎蟲數 增殖抑制率(%) 6週後 生存蟎蟲數 增殖抑制率(%) 實施例4-1 174 0 (97.5) f>99.9) 實施例4-2 206 168 0 (97.6) (>99.9) 比較例5 6,939 16,275 (評價) 若將實施例1-1、1-2、3-1、3-2、4-1、4-2與比較例1-1、1 -2、3、5進行比較,則得知各實施例可獲得具有優異 之防蟎蟲性的加工濾紙、加工合成皮革、加工布帛。 又,實施例4-1、4-2之加工布帛獲得了如下結果:抑制 了可於直徑為4 cm之圓形布料上(12_5 cm2)繁殖之約5,4〇〇 隻蟎蟲的繁殖。由於據稱塵蟎類(歐洲室塵蟎、美洲室塵 蟎)之每隻蟲屍會產生100 ng之Df過敏原(參照Mighty Checker(Sumika Enviro-Science股份有限公司)操作說明 書),故而抑制了相當於430 mg/m2之過敏原,可知與抗過 敏劑之減量有關《再者,蟎蟲抑制試驗係於適合塵蟎類生 長之條件下(25±2。(:、75 士 5%RH、有餌料)進行繁殖,其結 果並非一般條件下之增殖數。 152257.doc -39- 201138627 (抗過敏原試驗) 對實施例 1-1、1-2、3-1、3-2、4-1、4·2及比較例 1-1、 1-2' 3、4之滤紙、布帛、合成皮革實施抗過敏原試驗。 於針對實施例1 -1之加工濾紙之抗過敏原試驗中,預先Sugar, curcumin, coumarin, etc. I52257.doc 201138627 Examples of the synthetic high molecular phenols include polyphenylphenol and polyvinylphenol. Examples of the inorganic solid acid include a metal phosphate compound such as aluminum phosphate, a zeolite substituted with Y or the like, a composite oxide such as citric acid or Si〇2_A12〇3, magnesium citrate, zirconium phosphate, zirconium oxide, and ammonium zirconium carbonate. Or a zirconium compound such as potassium zirconium carbonate or an inorganic ion exchange product. Further, the ratio of the antibacterial composition to the antiallergic agent of the composition of the present invention is preferably from 3: 丨 to 丨: 5, and particularly preferably 丨: 3. When the compounding ratio of the antiallergic agent is more than the above range, when the composition is processed into a molded article, the texture of the molded article is lowered, and discoloration due to light or heat is likely to occur. On the other hand, if the compounding ratio of the antiallergic agent is less than the above range, it becomes impossible to obtain practical allergy deactivation performance. By setting such a specific mass ratio, the antibacterial property, the antifungal property, and the anti-mite property can be more effectively exhibited. As a result, even if the anti-allergic agent content is small, it can be made into a practical anti-allergy. Sexual composition. It is particularly preferred that the composition of the present invention contains an inorganic antibacterial agent and an aphid removing agent in addition to the antibacterial composition and the anti-allergic agent. Examples of the inorganic antibacterial agent include a copper compound such as copper sulfate, a zinc compound such as zinc oxide, a nickel compound, an inorganic metal compound such as a copper-nickel alloy, a metal-supporting zeolite, or a zirconium phosphate as a salt thereof. It is excellent in antibacterial and anti-fungal properties of silver-loaded strontium phosphate (silver-loaded zirconium phosphate-loaded silver zirconium phosphate). In addition to the antibacterial composition and anti-allergic agent in the composition of the present invention In the case where the inorganic antibacterial agent is also contained, the ratio of the antibacterial composition to the non-bacterial agent is 152257.doc 201138627. The ratio of the antibacterial agent is preferably 1.1 to 5. 1 and especially 2: 1. By setting such a specific mass ratio, it is possible to obtain an antibacterial molded article which is excellent in texture and is less likely to cause discoloration due to light or heat by adding a smaller amount of the composition, and can be efficiently obtained. The synergistic effect of the synergistic antibacterial action of the organic antibacterial agent of the imidazole type and the inorganic antibacterial agent is used in combination. Examples of the anti-insect agent include boron oxide or a glassy substance containing the same. Since boron oxide or a glassy substance containing the same is an inorganic compound, an antibacterial molded article which is less likely to cause discoloration than an organic compound and which is less likely to cause discoloration due to light or heat is obtained, and is further preferred. In addition to the antibacterial composition and the anti-allergic agent, the composition also contains the anti-allergic agent, and the ratio of the antibacterial composition to the aphid-removing agent is preferably 1:1 to 1:5 by mass ratio. More preferably, it is 1:3 c. By setting such a specific mass ratio, an antibacterial molded article excellent in aphid resistance can be obtained by adding a small amount of the composition. The composition of the present invention is shown in Table 1 to The microorganisms shown in Table 5, ie, fungi (fungi, bacteria, etc.) have antibacterial and antifungal properties. [Table 1] Fungi 1 Alternaria altemata 2 Aspergillus awamori 3 Aspergillus niger 4 Aspergillus oryzae 5 Aspergillus flavus I52257.doc 201138627 6 Aspergillus versicolor 7 Aspergillus fumigatus 8 Aspergi Llus nidulans 9 Aspergillus glaucus 10 Aspergillus terreus 11 Aspergillus phoenjcus 12 Aspergillus tamari 13 Aspergillus species 14 Confined Aspergillus restrictus 15 Aspergillus ochraceus 16 Aspergillus clavatus 17 Aspergillus ustus 18 Aspergillus candidus 19 Parasiticus Aspergillus parasiticus 20 Absidia corymbifera 21 Aspergillus luchensis 22 Absidia glauca 23 Fine chain Altemaria tenuis 24 Altemaria pisi 25 Altemaria candidus 26 Altemaria brassicicola 27 Aureobasidium pullulans 28 Ascosphaera apis 29 Ascomycetes Aphanomyces cochlioides 30 Aphanomyces raphani 31 Botrytis cinerea 32 Mycelium Byssochlamys nivea 33 Candida albicans 34 Beet Cerespora beticola 35 Cerespora musao 36 Claviceps purpurea 37 Colletotrichum trifolii 38 C. cerevisiae Ceratocystis cora 39 Chaetomium globosum 40 Cladosporium cladosporioides 41 Curvularia geniculata 42 Chrysosporium thermophilum 43 Candida guilliermondii 44 Candida lipolytica 45 Candida pelliculose 152257.doc -9- 201138627 46 Candida tropicalis 47 Candida glabrata 48 Candida acutus 49 Candida utilis 50 Cladosporium sphaerospermum 51 Cladosporium herbarum 52 Corticium rolfsii 53 Colletotrichum phomoides 54 Grass per charcoal Colletotrichum fragariae 55 Maltese anthracnose Colletotrichum atramentarium 56 Bean anthracnose Colletotrichum lindemuthianum 5 7 Fusarium oxysporum Ceratocystis ulmi 58 Clostridium acetobutylicum 59 Clostridium sporogenes 60 Cladosporium carpophilum 61 Curvularia lunata 62 Chrysosporium keratinophilum 63 Cryptococcus lutealus 64 New Cryptococcus neoformans 65 Cladosporium resinae 66 Cryptococcus albidas 67 Chaetomium clivaceum 68 Dactylium derdroides 69 Diplodia natalensis 70 Drechslera australiensis [Table 2] True 71 Eutopium tonophilum 72 Epicoccum purpurascens class 73 Euthium repens 74 E. sylvestris Eurotium rubrum 75 E. sylvestris Eurotium chevalieri 76 Amsterdam genus Eurotium amstelodami 77 Cellular Emericella nidulans 78 Exophiale jeanselmei 79 Fusarium semitectum 80 tip Fusarium oxysporum 81 Fusarium voseum 82 Fusarium moniliforme 152257.doc -10- 201138627 83 Fusarium solani 84 Fusarium roseum 85 Fusarium nivale 86 Fusarium avenaceum 87 Sharp top sickle Fusarium acuminatum 88 Fusarium proliferatum 89 Fusarium graminearum 90 Cotton root rot fungus Fhymatotricum omnivorum 91 White coat: Geotricham candidum 92 Geotricham lactus 93 Gliocladium virens 94 Glomerella cingulata 95 Long creep Helminthosporium sp. 96 Pedroca chromophyte Hormoderdrum pedrosoi 97 Helminthosporium gramineum 98 Lenzites trabea 99 Lenzites trabae 100 Lentinus lepideus 101 Medurella mycetomii 102 Microsporum canis 103 Microsporum gypseum 104 Microsporum audouini 105 Mucor racemosus 106 Myrothecixim verrucaria 107 Mucor mucedo 108 Mucor pusillus 109 Mucor spinescens 100 Mucor rouxii 111 Monascus ruber 112 Monilia Candida 113 Monilia fructigena 114 Monilia nigral 115 Rhizopus sinensis Monilia laxa 116 Menoniella echinita 117 Rhododendron fungus Neurospora crassa 118 Rhizoctonia solani Nigrospora oryzae 119 Neurospora sitophila 120 Neurospora sphaerica 121 Ocuremonium charticola 122 Penicillium frequentance 152257.doc -11 - 201138627 123 Penicillium citrinum 124 Penicillium variabile 125 Penicillium purpurogenum 126 Blue Penicillium glaucum 127 Amylopectin Pulluliana pullulans 128 Penicillium roquerforiti 129 Penicillium luteum 130 Penicillium expansum 131 Penicillium piscarium 132 Penicillium piscarium 132 Penicillium rugulosum 133 Penicillium cyclopium 134 Penicillium chrysium 134 Penicillium chrysium viride 136 Penicillium notatum 137 Penicillium rubrum 138 Penicillium oxalicum 139 Penicillium funiculosum 140 Penicillium digitatum [Table 3] 141 Penicillium islandicum 142 Penicillium nigricans 143 Penicillium lilacinum 144 Penicillium spinulosum 145 Smoke P. cerevisiae Pestalotia adusta 146 Infective P. sylvestris Pestalotia neglecta 147 Citrus Phomopsis Phomosis citri 148 Penicillium steckii 149 Citrus citricarpa 150 Pomegranate Phoma terrestius 151 Pomegranate Phoma Glomerata 152 P. sylvestris Phoma pigmentivora 153 Membrane Biqi Protozoa Pichia membranaefaciens 154 Peptococcus sp. 155 Proteus mirabilis 156 Phacidipycnus funfuracea 157 Phomopsis fukushii 158 Pythium debaryanum 159 Pythium irregulare 152257.doc -12- 201138627 160 Pythium aphanidermatam 161 Phomopsis vexan 162 Phytophthora megasperma 163 Phytophthora nicotianae 164 Phytophthora infestans 165 Phytophthora capsici 166 Phytophthora capsici 166 Plasmodiophora brassicae 167 Pyrenochaeta licopersici 168 Rhodotorula mimuta 169 Rhodotorula mucilaginosa 170 Rhodotorula texensis 171 Rhodotorula glutinis 172 Rhodotorula gulinis 173 Rhodotorula lactosa 174 Black Rhizopus nigricans 175 Rhizopus oryzae 176 Rhizopus rhizopus sto Ronifer 177 Rhizopus delemar 178 Rhizopus solani 179 Rhizopus javanicus 180 Sporotrichum shenki 181 Stichococcus bacillavis 182 Sclerotina fructincola 183 Saccharomyces cerevisiae ~~' Saccharomycodes pasteurianus 184 Streptomyces Stachybotrys sp. 185 Amorpha sclerotiorum Spicaria vlolacea 186 Scorecobasidium constrictum 187 Spiderosporium ~ ~ Scedosporium apiospermum 188 Synaptophyta " Syncephalastrum racemosum 189 Spirulina - 'Stachybotrys chartarum 190 S. schenkeii' Sporothrix schenckii 191 Onion white rot Sclerotium cepivorum 192 Sphaerotheca humuli 193 Sclerotinia sclerotiorum 194 Scutellaria " ~ Scopulariopsis brevicaulis 195 Bacteria " - Trichophyton mentagrophytes 196 Trichophyton gypseum 197 Trichophyton rubrum 198 Trichothecium ros Eum 199 Trichoderma viride 152257.doc •13- 201138627 200 Trichophyton ajelloi 201 Trichoderma koningii 202 Trichoderma T-1 203 Trichoderma harzianum 204 White globular yeast Tolulopsis Candida 205 Trichosporum cutaneum 206 Trichoderuma lignorum 207 Black-striped Ulocladium atrum 208 Ustilago zeae 209 Verticillium albo-atrum 210 Verticillium Dahliae 211 Wallemia sebi 212 Tyroyces palustris 213 Trametes versicolor 214 dried rot fungi Serpula lacrymans [Table 4] Fine 1 Alcaligenes faecalis 2 Alcaligenes viscolactis 3 Ascophyta pisi 4 Autotrophic bacteria 5 Aster yellows pathogen Astertobacter calcoaceticus 7 Achrcmobacter gulyatus 8 Aerobacter aer Ogenes 9 Aerobacter cloacae 10 Italian buds Blastomyces italicum 11 Cactus Bacillus cereus 12 Bacillus mycoides 13 Bacillus subtillis 14 Bacillus megaterrium 15 Bacillus anthracis 16 Bacillus punctatum 17 Bacterium vulgar. 18 Pseudomonas pyocyaneum 19 dermatitis Blastomyces dermatidis 20 Bacteridae fragilis 21 Campylobacter fetus 22 Clostridium perfringens Clostridium perfringens -14- 152257.doc 201138627 23 Clostridium difficile 24 lichens Corticium fuciforme 25 Clostridium botulinum 26 Clonecker apiculata 27 Cellulomonas iugis 28 Campylobacter jejuni/coli 29 Dactylium dendroides 30 Grapes Spore Diplodia viticol 31 Debaryamyces hansenii 32 Desulfovibrio desulfuricans 33 Endothia paracitica 34 Escherichia coli 35 Enterobacter aerogenes 36 Enterobacter clocae 37 Carrot soft rot fungus Erwinia carotovora 38 Clostridium faecalis Fusobacterium nucleatum 39 Flavobacterium aminogenes 40 Flammulina Fla Vobacterium meningosepticum 41 Gluconobacter suboxydans 42 Hansenula anomala 43 Klebsiella oxytoca 44 Klebsiella pneumoniae 45 Lactbacillus acidophilus 46 Lactobacillus planntarum 47 Listeria monocytogens 48 Legionella pneamophila 49 Leptospira interrogans 50 Coronal mushroom Lepiota criststa 51 Lepiota castanae 52 Lactobacillus bulgericus 53 Micrococcus glatamicus 54 Tuberculosis Mycobacterrium tuberculosis 55 Micrococcus albus 56 Micrococcus aquilis 57 Micrococcus conglomerates 58 Micrococcus varians 59 Paecilomyces lilacinus 60 Pudiococcus soyae 61 Pudiococcus acidilactici Pseudomonas Pseudomonas Aeruginosa 15225 7.doc -15- 201138627 63 Pseudomonas fluresceus 64 Paecilomyces variotii 65 Phaffia rhodozyma 66 Pichia anomala 67 Pichia membranaefaciens 68 Proteus Vulgaris 69 Pythium vanterpoolii 70 Phyrass cinereum 71 Propionibacterium aces 72 Propioniabacterium shermanii 73 Podospira leucotricha 74 Pseudomonos syringae 75 Pseudomonos solanacearum [Table 5] Fine 76 gas-producing Escherichia coli Paracolabactrum aerogenoides 77 Rhizoctonia violacea 78 Rhizoctonia solani 79 Rickettsia rickettsii 80 Ruminococcus 81 Scleotina scleotiorum 82 S. scleotolomyces roseus 83 Streptococcus lactis 84 Schizosacchar Omyces pombe 85 Ruthenium Saccharomycodes ludwigii 86 Serratia marcesens 87 Staphylococcus aureus 88 Salmonella typhimurium 89 Streptoverticum reticulum 90 Staphylococcus faecalis 91 Salmonella enterophylla Salmonella Enteritidis 92 Salmonella enterrica 93 Salmonella arizonae 94 Salmonella paratyphi 95 Salmonella choleraesuis 96 Streptococcus agalactiae 97 Serratia marcesceus Serratia liguefaciens 99 Saccharomyces cerevisiae 152257.doc -16- 201138627 100 Sugeran mosaic 101 Staphylococcus epidermidis 102 Staphylococcus hominis 103 Staphylococcus agalactiae 104 Staphylococcus pneumoniae 105 Staphylococcus pyogenes 106 Staphylococcus pyogenes 106 Serratia salinaria 107 Salmonella typhosa 108 Salmonella typhosa 109 Sarcina flava 109 Sarcina latea 100 Sporocytohaga myxococcoides 111 Black round yeast Torula nigra 112 Thermoactinomyces vulgaris 113 Thiobacillus asidophilus 114 Thiobacillus delicatus 115 Thiobacillus denitrificans 116 Thiobacillus ferrooxidans 117 Thiobacillus intermedius 118 Thiobacillus kabolis 119 Thiobacillus neapolitans 120 Thiobacillus neapolitans 120 Metabolism of Thiobacillus novellus 121 Thiobacillus perometabolis 122 Thiobacillus rubellus 123 Thiobacillus thiooxidans 124 Thiobacillus thioparus 125 Thiobacillus thermophilica imschenetskii 126 Thiobacillus versutus 127 Vibrio u Lnificus 128 Venturia inaequalis 129 Yersinia enterocolitica 130 Corynebacterium diphtheriae 131 Corynebacterium glutamicum A composition of the invention is derived, for example, from plant-derived allergens, from molds Allergens such as allergens, aphids, mites, or excrement, such as animal and plant proteins, exert anti-allergic properties. Further, the composition of the present invention is, for example, a dust mites such as the American house dust mites, the European house dust mites, the river glutinous rice glutinous rice, the long-haired whitefly, the elliptic powder, and the like, 152257.doc -17· 201138627 , Malacca meat worms, strong meat glutinous rice, common meat butterfly, scallops, and other meat worms such as 'Bai's poultry _, forest birds, chicken skin thorns, skin thorns and other poultry, ball belly (four), (four), etc. Out of the anti-wormworm, Next, the antibacterial treatment agent and the antibacterial molded article of the present invention (antibacterial treatment agent and antibacterial molded article) The antibacterial treatment agent of the present invention contains the composition of the present invention and a dispersion medium. Sprays, coatings, coating agents, surface treatment agents, and fiber treatment agents. Examples of the dispersion medium include lower alcohols such as water and methanol, polyethylene glycol, and polyethylene glycol. Further, in order to easily fix the composition of the invention to an adherend such as a fiber product, the adhesive is mixed with a binder. Acrylic resin, polyaminoethylene-vinyl acetate copolymer tree As the binder resin, for example, an acid ester, a polyoxyalkylene gas, a polyethylene gas, or a gas ester can be mentioned. It is preferable to use the antibacterial treatment agent of the present invention as a crosslinking agent. The crosslinking agent may, for example, be a nitrogen-containing blocked inert gas, a water-dispersed isocyanate, a melamine, an aqueous epoxy compound or a carbodiimide. The antibacterial treatment agent can be adhered, for example, by using the composition of the present invention, a dispersion medium, and the like. The agent is obtained by mashing and mixing. χ, the composition of the present invention may also be dispersed to a monomer of a propylene fluorene resin or a styrene monomer, or a mixture thereof; 5 when the shape is clear, after coating the antibacterial treatment agent, irradiating ultraviolet rays I52257 .doc 201138627 or heating to polymerize the monomer to harden the molded article. The bacteriostatic molded article of the present invention is a fiber product such as a fiber or a fabric which is treated by the one-line treatment of the antibacterial property of the present invention, and the enamel film is formed by laminating a fiber or a cloth on a resin film. (4) A factory for treating such a fiber product or the like with the anti-H treatment agent of the present invention, for example, a material which is to be adhered or used as a raw material of the raw material In the liquid fiber treatment agent of the composition of the invention, etc., the impregnation method includes so-called groove impregnation, etc. Further, the surface of the adherend is sprayed by a spray or the like. The method of coating, coating, and surface treatment agent which is one example of the antibacterial treatment agent of the present invention may be, for example, brushing or roll coating, printing by inkjet or letterpress, scattering, scraping or Various coating means such as spray coating, gravure coating, shower coating, and knife coating; or various printing means such as screen printing, pad printing, plate printing, inkjet printing, etc. Using the antibacterial property of the present invention Treatment agent Examples of the product include natural fibers such as cotton, |month, wool, and short fibers or long fibers such as polyester, nylon, acryl, synthetic fiber, semi-synthetic fiber, and regenerated fiber, and two types of fibers can be used. The above composite fiber 'may also be a fabric such as a woven fabric, a woven fabric, or a non-woven fabric. Examples of the resin film include PVC (polyethylene) or TP0 (lean tobacco elastomer) or PU (polyurethane). In addition, as the antibacterial molded article of the present invention, a resin film laminate such as synthetic leather, artificial leather, or tarpaulin provided with a fabric on the film may be mentioned. 152257.doc -19·201138627 The antibacterial molded article of the present invention contains the composition of the present invention and a resin, and may be formed by molding the resin. Examples of the resin include a molding resin, a fiber resin, a rubber resin, and the like. The mixture of the composition of the present invention and the resin is melted into a fiber or a film by a known molding method of stretching into a fiber shape or extrusion molding, thereby obtaining an antibacterial molded article of the present invention. system An antibacterial molded article of the present invention is obtained by a fiber product such as a fiber-containing fabric or a resin film laminated body obtained by laminating a film. As an example of the antibacterial treatment agent of the present invention, for example, it can be used as a household or industrial product. Coatings for interior and exterior materials, sprays for household or vehicle interiors, carpet cleaners, coatings or surface treatments for films or sheets, adhesives for fiber laminates, sand t, cement, wall materials In addition, as the adherend to be treated by the antibacterial treatment agent of the present invention, artificial leather processed by an adhesive for a fiber laminate, at least one of vinyl, paper, and cloth can be used. Wallpapers, building materials, wood, flooring, furniture for building and construction materials, aluminum panels for aluminum panels, aluminum alloys, resin moldings, toiletries, feed containers, air conditioning, air conditioning, air conditioning, air conditioning Road components, steel products, blankets, roofing materials, insulation materials, kitchen supplies, bathroom supplies, bedding, filters, furniture, paper 〇^ cookware, Skin 〇 〇 〇 (Effect of the embodiment) The composition of the present invention contains two kinds of imidazole-based antibacterial agents 152257.doc -20- 201138627 and anti-allergic agents, thereby inhibiting the cause of allergic substances The production of bacteria, mold, and aphids can make the content of the anti-allergic agent small, and exert the deactivation performance of the practical allergy-inducing substance. In particular, 'the antibacterial property can be obtained by using two imidazole-based organic antibacterial agents as a compound having a benzimidazole ring and a thiazolyl group, and a compound having a benzimidazole ring and an urethane group. Composition 0 which is more excellent in antifungal properties. Further, since the composition of the present invention further contains an inorganic antibacterial agent, the antibacterial property and the antifungal property can be further improved. In particular, by using an inorganic antibacterial agent as a silver-plated dish, a synergistic effect of the antibacterial action can be obtained, and a composition exhibiting more remarkable antibacterial and antifungal properties can be obtained. Further, since the composition of the present invention further contains an insecticide, the insecticidal property is further improved. In particular, the antibacterial property of the present invention is such that the antibacterial molded article containing the composition is less likely to cause discoloration due to light or heat by using the antimony agent as boron oxide or a vitreous material containing the same. The treatment agent contains the composition of the present invention and a dispersion medium, particularly a domestic spray, a paint, a coating agent, a surface treatment agent, and a fiber treatment agent. Therefore, it is easy to apply the composition to the adherend, and it is possible to produce an antibacterial treatment agent which is excellent in convenience. Further, since the antibacterial treatment agent of the present invention contains a binder resin, the composition can be effectively fixed to the adherend. Further, by using a crosslinking agent in combination, the fixing durability can be improved. That is, even if 152257.doc 21 201138627 is repeatedly washed, it is possible to maintain antibacterial, antibacterial, anti-insect, and anti-allergic properties for a long time. Further, the antibacterial molded article of the present invention is obtained by treating the fiber, the cloth, the resin film, or the laminate obtained by laminating the fiber or the cloth on the resin film by the antibacterial treatment agent of the present invention. Therefore, the application range is wide and the convenience is excellent. Further, since the antibacterial treatment agent of the present invention has a relatively small content of the anti-allergic agent, the antibacterial molded article treated with the antibacterial treatment agent has a good texture and is less likely to cause discoloration due to light or heat. Therefore, in general, there is room for cleaning. Further, the antibacterial molded article of the present invention contains the composition of the present invention and a resin, and may be formed by molding the same. Since the composition of the present invention has a small content of the anti-allergic agent, it can be made into an antibacterial molded article which is excellent in texture and which is less likely to cause discoloration due to light or heat. [Examples] Hereinafter, the present invention will be described more specifically by way of examples and comparative examples, but the present invention is not limited to the examples and the like. [Examples 1-1 to 4-2 and Comparative Examples 1 to 1 to 5] (Production of Antibacterial Treatment Agent and Antibacterial Shaped Product) Examples 1-1 to 4-2 and Comparative Examples 1_1 to 5 were It is implemented as follows. (Example 1-1) In Example 1-1, an aqueous spray was prepared in the following Production Example U, and the filter paper was processed using the aqueous spray of Production Example 1_1 in the following Production Example 1-2. Processing filter paper. I52257.doc •22·201138627 (Production Example 1-1) The (1A) to (3 A) of Table 6 were stirred and mixed in a beaker, and diluted to a volume of 1 L with distilled water (4A). The mixture was mashed and mixed for 20 minutes using LabStar LMZ06 (manufactured by Ashizawa Finetech Co., Ltd.) and using an oxide bead having a diameter of 0.5 mm. At this time, Sanxian gum was added at a time when the liquid viscosity became 700 mPa*s to 800 mPa*s, and an aqueous spray was prepared as an antibacterial treatment agent. (1A) Antibacterial composition 2-(4-thiazolyl)-1Η-benzimidazole (35 mass%), 1H-2-benzimidazolyl carbamate (35 mass%), and Mixture of silver-loaded zirconium phosphate (30% by mass) 3 g (2A) Anti-allergic agent Polyethylene (average molecular weight: 3,000) 4.5 g (3A) Dispersant Noigen TDS-100 (First Industrial Pharmaceutical Co., Ltd.) 3g (4A) Distilled water - 936 g (Manufacturing Example 1-2) Using a household sprayer, the amount of coating is 50 g/m2 for the filter paper (8:8) 2. 2) Spraying the aqueous spray of Production Example 1-1 to prepare a processed filter paper. Using the processed filter paper, the following antibacterial test was performed. (Example 1-2) In Example 1-2, except A processed fabric was produced in the same manner as in Example 1-1 except that the filter paper was changed to a polyester woven fabric (Tricot fabric basis weight: 320 g/m 2 ). The following antibacterial test was carried out using the processed fabric $ (Example 2) -1) 152257.doc •23·201138627 In Example 2-1, the fiber treatment agent was prepared in the following Production Example 2-1, and the fiber treatment agent of Production Example 2-1 was used in the following Production Example 2-2. machining The fabric was produced, and the following antibacterial property test was carried out. (Production Example 2_1) After combining and mixing (1B) to (3B) of Table 7 in the beaker, the above-mentioned LabStar LMZ06 was used and the diameter was 〇. A 5 mm zirconia bead was ground and mixed for 30 minutes to prepare a fiber treating agent. [Table 7] (1B) Antibacterial composition 2-(4-thiazolyl)-iH-benzopyrene (50% by mass) ) a mixture with methyl 1H-2-benzimidazolylamine decanoate (50% by mass) 180 g (2B) Antiallergic agent Polyphenon 70A (Mitsui Nonglin Co., Ltd.) 20 g (3B) Adhesive resin Light Epoch AX- 30 (Hokko Chemical Co., Ltd.) 300 g (Production Example 2-2) The fiber treating agent of Production Example 2 - 1 was diluted to a capacity of 20 times with distilled water, and the cloth of size A4 was treated with fiber in a metal crucible. The solution was immersed for 5 seconds. Here, the cloth was made of a standard cotton woven cotton cloth No. 3. Then, it was extruded by a roller press having a pressure between rolls of 4.0 kg/cm 2 (extrusion rate: 100%). The fabric of Example 2-1 was produced by drying with a hot air dryer at a temperature of 120 ° C for 10 minutes. 2-2) In Example 2-2, a fiber treating agent was prepared in Production Example 2-1, and a fabric was processed in the following Production Example 2-3 using the fiber treating agent of Production Example 2-1, thereby producing a processed fabric. And the following antibacterial test and the like were carried out. 152257.doc •24_ 201138627 (Manufacturing Example 2-3) The fiber treating agent of Production Example 2 - 1 was diluted to a capacity of 丨〇 times with distilled water, and the cloth of size Α4 was impregnated into the fiber containing in the metal drum. The solution of the treatment agent was for 5 seconds. Here, the fabric is Nylon (Nyl〇n, basis weight 110 g/m2). Then, extrusion was carried out using a roller compactor with a pressure between the rolls of 4 〇 kg/m2 (extrusion rate: 5〇%), using a hot air dryer at i2〇 The film of Example 2-2 was produced by drying at a temperature of <>c for 2 minutes and heat-treating at 150 °C for 丨min. (Example 2-3) In Example 2-3, a fiber treating agent was prepared in Production Example 2, and the fabric was processed in the following Production Example 2-4 using the fiber treating agent of Production Example 2_ The fabric is processed, and the following antibacterial test is performed. (Manufacturing Example 2-4) The fiber treating agent of Production Example 2-1 was diluted to a capacity of 15 times by using distilled water. The cloth of the size A4 was immersed in a solution containing the fiber treating agent in a metal drum for 5 seconds. bell. Here, the fabric is a polyester/cotton blend (65 〇/./35%) plain weave 2 structure (basis weight 120 g/m2). Then, 'the extrusion was carried out using a roller compactor having a pressure between the rolls of 4 〇kg/m 2 (extrusion ratio: 7〇%)', which was dried for 3 minutes at the temperature of the bribe, and heat-treated under the armpit. This production example 2-3 Processing cloth. (Example 3-1) In Example 3, a surface treating agent was prepared in the following Production Example 3_丨, and a fiber treating agent was prepared in the following Production Example 3-2. Further, in the production example μ, the synthetic surface leather was produced by using the surface treatment agent of Production Example 3 and the fiber treatment agent of Production Example 3_2, and 152257.doc • 25·201138627 synthetic leather. (Production Example 3-1) (1C) and (2C) of Table 8 were sufficiently mixed in a powder state, and the mixture was added to (3C), and stirred and mixed by AGI Homomixer (manufactured by Primix Co., Ltd., TK Robomix). A surface treatment agent for an antibacterial treatment agent for synthetic leather was prepared for 5 minutes. (1C) Antibacterial composition 2-(4-thiazolyl)-1Η-benzimidazole (35 mass%), 1H-2-benzimidazolylamine decanoate (35 mass%), And a mixture of silver-containing male acid (30% by mass) 0.025 g (2C) mixture of anti-allergic agent zirconium phosphate (70% by mass) and tannic acid (30% by mass) 1.0 g (3C) treating agent Leatheroid LU- 4305SP (Daily Seiki Co., Ltd.) 100 g (Production Example 3-2) Using the above-mentioned LabStar LMZ06 and using 0.5 mm diameter cerium oxide beads, the (3D) distilled water is used to dilute (1D) and (1) 2D) The mixture was mashed and mixed for 20 minutes to prepare a fiber treatment agent for synthetic leather. [Table 9] (ID) Anti-mite agent Glass powder containing boron oxide (10% by mass) 20 g (2D) Adhesive resin Evafanol AS-21 (曰华化工股份有限公司) 200 g (3D) Distilled water - 780 g ( Production Example 3-3) First, 2 g of the fiber treating agent of Production Example 3-2 was uniformly sprayed on the back surface (base fabric side) of a synthetic leather having a size of 20 x 20 cm, using a hot air dryer at 152257.doc -26 - Dry at 201138627 110 C for 5 minutes. Then, the surface treatment agent 4 g' of the production example 3_丨 was applied to the surface (silver side) by a bar coater again. Dry at <t for 5 minutes. As a result, a synthetic leather was produced as an antibacterial molded article of Example %. The synthetic leather was made of a silver-based surface made of polyacrylic acid S-ruthenium and the base fabric was PET (poly-p-butyl phthalate). 〇〇% 编 帛 。. (Example 3-2) A surface treating agent was prepared in Production Example 3-1 in Example 3-2, and a fiber treating agent was prepared in the following Production Example 3-2. In the production example 3_4, the synthetic leather was processed by using the surface treatment agent of Production Example 3-1 and the fiber treatment agent of Production Example 3-2. (Production Example 3-4) First, 2 g of the fiber treating agent of Production Example 3-2 was applied to the back surface (base fabric side) of a synthetic leather having a size of 20 x 20 cm by a gravure roll, and a hot air dryer was used at 110 ° C. Dry at the temperature for 5 minutes. Then, 4 g of the surface treatment agent of Production Example 3-1 was applied to the surface (silver side) by a bar coater, and dried again at a temperature of 110 ° C for 5 minutes. Thus, a processed synthetic leather which is an antibacterial molded article of Example 3-2 was produced. Synthetic leather is made of a silver surface made of polyamino phthalate and the base fabric is a nylon 100% woven fabric. (Example 4-1) In Example 4-1, a fiber treating agent was prepared in the following Production Example 4-1, and the fiber treating agent was used in the following Production Example 4-2. Thereby making a processing fabric. (Production Example 4-1) 152257.doc •27·201138627 The mixture of (1E) to (3E) of Table 10 was diluted with distilled water (4E) in a beaker and stirred, and the above-mentioned LabStar LMZ06 was used and the diameter was used. The 0.5 mm zirconia beads were mashed and mixed for 30 minutes to prepare a fiber treating agent as an antibacterial treating agent. (1E) Antibacterial composition 2-(4-thiazolyl)-1Η-benzimidazole (35 mass%), 1H-2-benzimidazolylamine decanoate (35 mass%), And a mixture of silver-loaded yttrium phosphate (30% by mass) 60 g (2E) Anti-allergic agent cerium oxide 75 g (3E) Dispersing agent Noigen TDS-100 (First Industrial Pharmaceutical Co., Ltd.) 60 g (4E) Distilled water - 855 g (Production Example 4-2) The fiber treatment agent (35 g) of Production Example 4-1, the Neostecker SI (10 g) manufactured by Shunhua Chemical Co., Ltd., and 455 g of distilled water were mixed, and the size was set in a metal drum. The fabric of A4 was immersed in a solution containing a fiber treatment agent for 10 seconds. Here, the fabric is a PET 100% Tricot fabric having a basis weight of 270 g/m2. Then, extrusion was carried out using a roller compactor having a pressure of 4.0 kg/cm 2 (extrusion ratio: 95%), and dried by a hot air dryer at a temperature of 120 ° C for 10 minutes. Thus, a processed fabric as an antimicrobial molded article of Example 4-1 was produced. (Example 4-2) In Example 4-2, a fiber treating agent was prepared in Production Example 4-1, and a fiber treating agent was used in the following Production Example 4-3 to process a fabric. Make and process fabrics. 152257.doc -28-201138627 (Production Example 4-3) The fiber treatment agent (35 g) of Production Example 4-1, Neosetker SI (10 g) manufactured by Rihua Chemical Co., Ltd., and Yuhua Chemical Co., Ltd. Manufactured * anti-imine-imine cross-linking agent NK Assist Cl 1 0 g (crosslinking agent) and steamed water 445 g mixed, the fabric of size A4 was immersed in the metal barrel to the solution containing the fiber treatment agent 1 second. Here, the cloth is made of PET 100% Tricot fabric having a basis weight of 270 g/m2. Then, extrusion was carried out by means of a press machine having an inter-roller pressure of 4.0 kg/cm (extrusion ratio: 95%), and dried by a hot air dryer at a temperature of 120 C for 1 minute. Thus, a processed fabric as an antibacterial molded article of Example 4-2 was produced. (Comparative Example 1-1) In Comparative Example 1-1, the same as the filter paper used in Example U was prepared and was not spray-processed. (Comparative Example 1-2) In Comparative Example 1-2, the same as the polyester woven fabric used in Example 1-2 was prepared and was not spray-processed. (Comparative Example 2-1) In Comparative Example 2-1, a fiber treating agent was prepared in the following Production Example 5-1, and the fabric was processed in the following Production Example 5-2 using the fiber treating agent of Production Example 5, This is used to make processing cold. (Production Example 5-1) After mixing and stirring (1F) to (3F) of Table 11 in a beaker, the above-mentioned LabStar LMZ06 was used and pulverized by a oxidized conical bead having a diameter of 5 Å, for 3 minutes. A fiber treatment agent is prepared. σ 152257.doc -29- 201138627 [表Η] (IF) Antibacterial composition zinc pyrithione 1 OA (2F) anti-allergic agent Polyphenon 70A -- 20 g (Mitsui Nonglin Co., Ltd., (3F) Adhesive Resin Light Epoch AX-30 300 g (Hokko Chemical Co., Ltd.) (Production Example 5-2) The fiber treating agent of Production Example 5-1 was diluted to a capacity of 2 times with distilled water, and the size was A4 in a metal drum. The fabric was immersed in a solution containing a fiber treatment agent for 5 seconds. Here, the cloth was made of a standard cotton woven cotton cloth No. 3. " Then, the squeezing was carried out using a roller press having a pressure between rolls of 4.0 kg/cm2. (Extrusion ratio: 1% by weight), and dried in a hot air dryer at 12 (minute at rc temperature to prepare a processed cloth of Comparative Example 2-1. (Comparative Example 2-2) In Comparative Example 2-2 In the production example, a fiber treatment agent was prepared, and the fabric was processed using the fiber treatment agent of the production example w in Production Example 5-3, thereby producing a processed fabric, and the following antibacterial property test was carried out. (Production Example 5-3) The steaming water will dilute the fiber treatment agent of the manufacturing example 5 _ 1 to the capacity of i 〇, and the size of the gold (four) is A4. The cloth was immersed in a solution containing a fiber treating agent for 5 seconds. Here, the cloth was spun nylon. Then, the press was performed using a press machine having a pressure between rolls of 〇kg/cm2 (extrusion ratio: 50%) 'Using a hot air dryer at 12 () t clock' under (10) heat treatment for 1 minute, thereby producing Comparative Example 2: 152257.doc -30- 201138627 Fabric. (Comparative Example 2-3) Comparative Example 2-3 In the production example 5_丨, a fiber treatment agent was prepared, and in the production example 5·4, the fabric was processed using the fiber treatment agent of the production example 5_丨, thereby producing a processed fabric. ' (Production Example 5-4) Using distilled water The fiber treating agent of Production Example 5-1 was diluted to a capacity of 15 times. The cloth of size A4 was dipped in a solution containing the fiber treating agent in a metal drum for 5 seconds. Here, the cloth was polyester/ Cotton mixed (65%/35%) plain weave (weight: 120 g/m2). Then, it is extruded by a pressure-sensitive machine with a pressure between rolls of 4 〇kg/m2 (extrusion rate: 7〇%). It was dried by a hot air dryer at a temperature of 120 ° C for 3 minutes, and heat-treated at ISO t for 丨 minutes to prepare a processed fabric of Comparative Example 2-3 (Comparative Example 3). In Comparative Example 3, in the production example 3-3 of Example 3-1, the fiber treatment agent was not sprayed on the back side of the synthetic leather, and 4 g of Leatheroid LU-4305SP (manufactured by Otsuka Seika Chemical Co., Ltd.) was applied instead of the production example. In the same manner as in Example 3-1, an unprocessed synthetic leather of Comparative Example 3 containing no antibacterial composition, anti-allergic agent, or anti-mite agent was prepared except that the surface treatment agent of the crucible was used. (Comparative Example 4) In Comparative Example 4, in the production example 4-1 of Example 4-1, the (4 £) laughter water of Table 1 was increased to 930 g without using (2E) cerium oxide of Table 10. (75) A fiber treatment agent J 0 152257.doc -31·201138627 was prepared under the same conditions as in Production Example 4-1, and the prepared fiber treatment agent (35 g), manufactured by Rihua Chemical Co., Ltd. A processing fabric was produced under the same conditions as in Production Example 4-2 except that Neostecker SI (10 g) was mixed and used as a solution containing a fiber treating agent. (Comparative Example 5) In Preparation Example 5, 'Preparation and Example 4_ 1 PET 100% Tricot fabric used is the same and unprocessed. Secondly, 'antibacterial test' of the molded articles of the examples and comparative examples' anti-fungal test, aphid inhibition test and anti-allergen test. (Antibacterial test) Antibacterial tests were carried out on the fabrics of Examples 2-1 to 2-3, 4-1, 4-2 and Comparative Examples 2-1 to 2-3, 5. The antibacterial test was based on JIS_L_ 1902 (2002) It is carried out by the absorption method. The strains use Staphylococcus aureus and Klebsiella pneumoniae, in Examples 2-1 to 2-3, 4-1, 4- 2 and Comparative Example. 2-1 to 2-3, 5 cloth and cotton standard white cloth were inoculated with the bacterial liquid, and the bactericidal activity value was calculated using the following formula (number); the results are shown in Table 12. Bactericidal activity value = Log(a/b)...(Number 1) a : Number of bacteria immediately after inoculation of cotton standard white cloth b: Number of bacteria after 18 hours of cloth culture. 152257.doc -32· 201138627 [Table 12] Sample sterilization activity * 1± Value S. aureus K. pneumoniae Example 2-1 L. Processed fabric (close-knit cotton No. 3) > 1.5 1.4 Example 2-2 Processed fabric (nylon) > 1.5 1.3 Example 2-3 Processed fabric (polyester /cotton) >1.5 1.4 Comparative Example 2-1 Processing fabric using other antibacterial agents (close-knit cotton cloth No. 3) > 1.5 1.2 Comparative Example 2-2 Processing fabric using other antibacterial agents (nylon) >1.5 1.2 Comparison Example 2-3 Processed fabric using other antibacterial agents (polyester/cotton) > 1.5 1.1 Example 4-1 Processed fabric (PET Tricot) 1.2 > 1.5 Example 4·2 Processed fabric (PET Tricot) 1.3 > 1.5 Comparative Example 5 Unprocessed fabric (PET Tricot) -1.0 -0.8 If Examples 2-1 to 2-3, 4-1, and 4-2 are compared with Comparative Examples 2-1 to 2-3 and 5, then Got : Examples 2-1 to 2-3,4-1,4-2 because it contains 2- (4- ° saliva plug-yl) lH-benzo sings and discharge 1H-2- benzimidazole. By sitting on the guanidinium decanoate, a processed cloth having excellent antibacterial properties is obtained. On the other hand, it was found that Comparative Example 5 does not have antibacterial properties because it does not contain the antibacterial composition of the present invention. Further, 'Comparative Examples 2-1 to 2-3 have a general antibacterial agent other than the present application, and therefore have been confirmed to have antibacterial properties. (Antifungal performance test) For Examples 1-1, 1-2, and 2-1 2-3, 3-1, 3-2, 4-1, 4-2 and Comparative Examples 1-1, 1-2, 2-1 to 2-3, 3 filter paper, synthetic leather, fabric anti-fungal performance test. The furnace and paper of Example 1-1 were sprayed at room temperature for one hour using a spray prepared by using the prepared aqueous spray. A 3 cm x 3 cm square was cut out from the center of the crepe paper, and the spray surface was used as the front side to carry out the following 20-method antifungal performance test. Further, the paper of Comparative Example 1-1, which was not sprayed with a water-based nozzle, was similarly cut into 3 cm><3 cm square' performed the following two methods of antifungal activity 152257.doc -33-201138627. For the synthetic leathers of Examples 3-1, 3-2 and Comparative Example 3, 3 cm x 3 cm square was cut out, and the silver surface was used as the front side, and the following 20-method mold-proof performance test was carried out. For the fabrics of Examples 1-2, 2-1 to 2-3, 4-1, 4-2 and Comparative Examples ι. 2, 2-1 to 2-3, 3 cm was also taken. <3 cm square, the following 20-method anti-fungal performance test was carried out. In the mold-proof performance test, the test bacteria shown in Table 14 were used, and the examples 1 _ 1, 1 _2, 2-1 to 2-3, 3-1, 3-2 were confirmed according to the following test methods and criteria. The antifungal properties of 4-1, 4-2 and Comparative Examples 1-1, 1-2, 2-1 to 2-3, 3. (Method for testing mold resistance) (Preparation of culture medium) (1) The medium used for the mold resistance test was used in JI; S-type medium was added with potato dextrose culture solution (Potato Dextrose Broth, manufactured by Difco Co., Ltd.) The plate medium was composed as shown in Table 13 below. This was heat-sterilized at 121 ° C for 2 Torr. (Composition of medium) [Table 13] 1.000 ml 3-0 g 10 g 0-5 g 0.25 g 0.002 g 7.0 g 25 g Purified water ammonium nitrate potassium dihydrogen phosphate magnesium nitrate heptahydrate potassium sulfate iron (II) Heptahydrate potato dextrose broth (manufactured by Difco Co., Ltd.) Agar 152257.doc -34 201138627 (Preparation of test bacterial solution) (2) The test bacteria of Table 14 were inoculated in the medium prepared in (1), and sufficiently cultured. 20 ml of the wetting solution of the composition of the following Table 15 was added to the culture dish to recover the spores. After the spore solution was filtered, the number of spores was prepared to be lxl06±1 / 'mL. When the spore concentration is high, the composition liquid obtained by removing agar from the above JIS standard medium is diluted. (Types of test bacteria) [Table 14] 1 Alternaria 2, black fungus 3, variegated fungus 4, soil fungus 5, rot fungus, Aureobasidium pullulans, 7 globosa, 8 genus Cladosporium 9 Fusarium sporogenes 10 Vibrio genus 11 Fusarium oxysporum 12 Myxosporium fungus 13 Scleroderma sinensis 14 Rhizoctonia solani 15 Paecilomyces variabilis 16 Penicillium citrinum 17 Penicillium funiculosum 18 Purple cocci 28 small Mycelium 20 Trichoderma viride (composition of moisturizing liquid) [Table 15] Purified water 1,000 ml Sodium dioctyl sulfosuccinate 0.05 g 152257.doc -35· 201138627 (culture) · Prepared in (1) After the spore liquid prepared in (2) was inoculated on the medium, the synthetic paper of the filter papers of Examples 1-1 and 1-1, and the synthetic leathers of Examples 3-1, 3-2 and Comparative Example 3 were respectively carried thereon and carried out. After processing fabrics of Examples 1-2, 2-1 to 2-3, 4-1, 4-2 and Comparative Examples 1-2 and 2-1 to 2-3, using a circulator with a humidity temperature controller, The temperature was maintained at 29 ± 1 ° C, and the humidity was maintained at 85% R · Η or higher for 28 days. Further, the growth status of the mold was visually confirmed weekly (confirmed on the first week, the second week, the third week, and the fourth week after the start of the culture), and evaluated according to the five evaluation levels shown in Table 16 below. The results are shown in Table 17. [Table 16] Evaluation of bacterial growth on the surface of the sample 0 Bacteria did not grow at all 1 10% or less Growth 2 10 to 30% or less Growth 3 30 to 60% or less Growth 4 60% or more completely grown [Table 17] Samples 1 week later 2 weeks After 4 weeks after 3 weeks, Example 1-1 Processing filter paper 0 0 0 0~1 Example 1-2 Processing cloth 0 0 0 0 Comparative example 1-1 Processing paper 2 3 4 4 Comparative example 1-2 Processing cloth 2 3 4 4 Example 2-1 Processed fabric 0 0 0 0 Example 2-2 0 0 0 0 Example 2-3 0 0 0 0 Comparative Example 2-1 Other antibacterial agent processing cloth 0 1 3 3 Comparative Example 2 -2 0 1 3 3 Comparative Example 2-3 0 1 3 3 -36- 152257.doc 201138627 After 1 week, 2 weeks, 2 weeks later, 2 4, Deutsche, Example 3-1, processed synthetic leather 0 〇 1 Λ Example 3-2 Processed synthetic leather (gravure) 0 0 〇U π Comparative example 3 Unprocessed synthetic leather 1 2 3 U 实施 Example 4-1 Processed fabric—0 0 0 J Λ Example 4-2 0 0 0 U 0 Right Comparing the examples 1 -1 1-2, 2-1 to 2-3, 3-1 3_2, 4-1, 4-2 with the comparative examples M, i-2, W to 2_3, 3, It is understood that each embodiment can obtain filter paper having excellent mold resistance, synthetic leather, Silk. On the other hand, it was found that each of the comparative examples did not have antifungal properties because it did not contain the antibacterial composition of the present invention. (Spiral Inhibition Test) 1-2, 3-1, 3-2, 4-1, 4_2 and Comparative Examples Aphid inhibition was carried out on the filter paper, synthetic leather, and cloth of Examples 1-1, i-2, 3, and 5. test. According to the JIS_L_1920 proliferation inhibition test a method, the aphid test examples 丨 to 3 were carried out as a tapeworm inhibition test. Specifically, the worm is a European house dust worm (the Tokyo Women's University). The paper, synthetic leather, and cloth (4) of the examples and comparative examples cut into a diameter of 4 (10) were placed on a petri dish, and a mites medium containing 7 〇 ± 1 。 was seeded thereon. Thereafter, the cells were cultured at 25 ± 2 and 75 ± 5% RH2 j , and the number of aphids in the fourth and sixth weeks was counted, and the total number of survivals was determined three times. The growth inhibition rate was calculated from the average survival number obtained and the following formula (number 2). Proliferation inhibition rate (%) = 10 〇 x (cd) / c (number 2) C: Average survival number on unprocessed molded articles (filter paper, synthetic leather, fabric) d. Processed molded articles (filter paper, synthetic leather, Average survival number on the cloth (Vibrio sinensis test example 1) 152257.doc • 37- 201138627 In the aphid test example 1, the processing filter paper of Example 1-1 having a diameter of 4 cm and the comparative example 1-1 were used. The sprayed unprocessed filter paper was used as a sample and tested by the above method. Further, the processed synthetic leather of Example 1-2 and Comparative Example 1-2 was used as a sample, which was cut into a circular shape having a diameter of 4 cm and the base fabric was faced upward, and the test was carried out in the above manner. The results after 6 weeks are shown in Table 18. [Table 18] Survival cochlear number proliferation inhibition rate (%) after 6 weeks of initial survival of locusts Example 1-1 225 2 > 99.9 Example 1-2 3 > 99.9 Comparative Example 1-1 6,977 • Comparative Example 1 -2 7,023 - (Aphid test example 2) In the aphid test example 2, the processed fabric of Examples 3-1 and 3-2 and the unprocessed synthetic leather of Comparative Example 3 were used as a sample, and cut into a diameter of 4 cm. The test was carried out by rounding the base fabric face up. The results after 4 weeks and 6 weeks are shown in Table 19. [Table 19] Inhibition rate of survival of aphids after 4 weeks of initial survival of aphids (%) Proliferation inhibition rate of survival of aphids after 6 weeks (%) Example 3-1 223 9 (99.8) 28 (99.7) Example 3 2 8 (99.8) 27 (99.7) Comparative Example 3 3,894 10,920 (Aphid Test Example 3) 152257.doc -38 - 201138627 In the aphid test example 3 'Working fabrics and comparative examples using Examples 4_1, 4-2 The unprocessed fabric of 5 was used as a sample 'cut it into a circle having a diameter of * cm and tested by the above method. The results after 4 weeks and 6 weeks are shown in Table 20. [Table 20] Inhibition rate of survival of aphids after 4 weeks of initial survival of aphids (%) Proliferation inhibition rate of survival of aphids after 6 weeks (%) Example 4-1 174 0 (97.5) f>99.9) Example 4- 2 206 168 0 (97.6) (>99.9) Comparative Example 5 6,939 16,275 (Evaluation) If Examples 1-1, 1-2, 3-1, 3-2, 4-1, 4-2 and Comparative Examples When 1-1, 1 - 2, 3, and 5 were compared, it was found that each of the examples can obtain processed filter paper having excellent anti-mite properties, processed synthetic leather, and processed fabric. Further, the fabrics of Examples 4-1 and 4-2 obtained the following results: the reproduction of about 5, 4 ticks which can be propagated on a circular cloth having a diameter of 4 cm (12_5 cm2) was suppressed. Since it is said that each corpse of dust mites (European house dust mites, American house dust mites) will produce 100 ng of Df allergen (refer to Mighty Checker (Sumika Enviro-Science Co., Ltd.) operating instructions), it is suppressed Corresponding to 430 mg/m2 of allergen, it is known to be related to the reduction of anti-allergic agents. In addition, the aphid inhibition test is suitable for the growth of dust mite (25±2. (:, 75 ± 5% RH, The bait) was propagated, and the result was not the number of proliferation under normal conditions. 152257.doc -39- 201138627 (anti-allergen test) For Examples 1-1, 1-2, 3-1, 3-2, 4-1 The anti-allergen test was carried out on the filter paper, the cloth, and the synthetic leather of Comparative Example 1-1, 1-2' 3, and 4. In the anti-allergen test for the processing filter paper of Example 1-1,

利用碟酸缓衝液將Mite Extract-Df(美洲室塵蟎:COSMO BIO股份有限公司製造)之濃度稀釋為8 pg/ml。並且,切取 20 cm2之實施例1-1之加工濾紙置於試驗管中,繼而添加上 述稀釋過敏原溶液3.5 ml,而浸潰加工滤紙。於水溫為 3 7 C之水浴中振盈混合24小時以上。其後,採取試驗管内 之 /谷液0.1 ml ’ 將其滴加至Mighty Checker(Sumika Enviro.The concentration of Mite Extract-Df (American House Dust Mites: manufactured by COSMO BIO Co., Ltd.) was diluted to 8 pg/ml using a dish acid buffer. Further, 20 ml of the processed filter paper of Example 1-1 was cut out and placed in a test tube, followed by the addition of 3.5 ml of the above-mentioned diluted allergen solution, and the filter paper was impregnated. Mix in a water bath with a water temperature of 3 7 C for more than 24 hours. Thereafter, 0.1 ml of the /colum solution in the test tube was taken and added to the Mighty Checker (Sumika Enviro.

Science股份有限公司製造)之萃取液浸潰部。水平放置ι〇 分鐘後,根據檢測線窗口之顯色狀態判定過敏原之去活 化。再者 藉由與 ,檢測線窗口之判定係藉由如下方式進行評價 實施例1-1相同之方式,對實施例卜2、、Extracted by the Science Co., Ltd.). After 〇 水平 horizontally, the allergen is deactivated according to the color status of the detection line window. Furthermore, the determination by the AND and the detection line window is performed in the same manner as in the following embodiment, and the embodiment is as follows.

合成 2、4-1、4-2及比較例“、n 3、4之濾紙、布 皮革實施抗過敏原試驗。將其結果示於表2ι。 (檢測線窗口之判定) 於通常情況 ++:顏色深且較粗之清晰線條«敏原多 需除去) + :可知線條清晰(一般家庭之通常水平) .可知隱約顯色(良好之水平) _··完全未顯色(非常令人滿意之水平) I52257.doc 201138627 [表 21] 試料 判定 實施例1-1 加工濾紙 比較例1-1 未加工渡紙 ++ 實施例1-2 加工布料 比較例1-2 未加工布料 實施例3-1 加工合成皮革 實施例3-2 比較例3 未加工合成皮革 ++ 實施例4·1 加工布料(PET Tricot) 實施例4-2 - — 比較例4 加工布料(無抗過敏劑、PET Tricot) •H- (評價) 可知,實施例1-1、1_2、3-1、3-2、4-1、4-2由於含有本 發明之組合物,故而獲得抗過敏性優異之加工濾紙、加工 布帛、加工合成皮革。另一方面,比較例3由於不含有作 為抗過敏劑之磷酸鍅’故而抗過敏試驗之判定遜於實施例 3-1、3-2。又,可知:比較例4雖含有2-(4-β塞嗤基)_iH-苯 并咪唑、1H-2-苯并咪唑胺基曱酸甲酯、及腐絕 (Thiabendazole),但不含有作為抗過敏劑之氧化锆,故而 抗過敏性遜於實施例4-1、4-2。 (交聯劑之耐久性) 又’為了確認交聯劑之耐久性提昇效果,依據JIS l 0217-103法’對實施例4-1、4-2及比較例4之PET 100% Tricot布料進行規定次數之家庭洗滌處理(JIS [ 0217_ 103 :家庭洗滌條件)。 於適合上述JIS規格之家用洗衣機中加入溫度為4〇χ:之 水’以相對於1 L水為2 g之比例添加衣料用合成洗劑,將 152257.doc • 41 - 201138627 其溶解製成洗滌液。 以浴比成為1 : 30之方式向該洗滌液中投入試料及視需 要之負載布,開始運轉。 處理5分鐘後,停止運轉,利用脫水機將試料及負載布 脫水,繼而將洗滌液換為常溫之新的水,以相同之浴比沖 洗2分鐘。沖洗2分鐘後,進行脫水,在不受日光直射之狀 態下晾乾。 其後,對實施例4-1、實施例4-2、比較例4之PET 100% Tricot布料實施抗菌性試驗、防黴菌性試驗、蟎蟲抑制試 驗、抗過敏原試驗。將其結果示於表22、23。 再者,於表22、23中,10HL表示進行10次家庭洗滌之 情形,30HL表示進行30次家庭洗滌之情形。 [表 22] 抗菌性試驗 防黴菌性能試驗 殺菌活‘ ft值(黃色葡萄球菌) 4遇 後之5個等級之評價 初期 10HL 30HL 初期 10HL 30HL 實施例4-1 >1.5 0.7 -0.1 0 0〜1 2 實施例4-2 >1.5 >1.5 >1.5 0 0 0 比較例4 -1.0 -1.2 -1.2 4 4 4 [表 23] 蟎蟲抑制試驗 抗過敏性試驗 增殖抑制率(%) Mighty Checker法 初期 10HL 30HL 初期 10HL 30HL 實施例4-1 >99.9 90.0 70 - 士 + 實施例4-2 >99.9 >99.9 97.3 _ - 比較例4 - - - ++ ++ -H- (評價) 152257.doc -42- 201138627 得知實施例4_2由於除了本發明之組合物以外,亦含有 交聯劑’故而即使洗務30次以上’亦保持抗菌性、防黴菌 性、防蟎蟲性、抗過敏性。另-方面得知,不含有交聯劑 之實施例4·1與實施例4-2相比,未保持抗菌性、防黴菌 性、防蜗蟲性、抗過敏性。 再者,比較例4雖然含有2·(4·噻唑基)_1Η_苯并咪唑、 1Η-2-笨并咪唑胺基甲酸曱酯、及腐絕,但不含有氧化 口因此得知,對於比較例4,洗滌丨〇次以上時之抗菌 ^防黴菌性、防蟎蟲性、抗過敏性遜於實施例1、4-2 ° 152257.doc •43-Synthesis of 2, 4-1, 4-2 and Comparative Examples ", n 3, 4 filter paper, cloth leather anti-allergen test. The results are shown in Table 2 (determination of the detection line window) in the usual situation ++ : Clear and thicker clear lines «Minami needs to be removed» + : It is clear that the lines are clear (usually the average level of the family). It is known that the faint color (good level) _·· completely uncolored (very satisfactory) Level) I52257.doc 201138627 [Table 21] Sample Determination Example 1-1 Processing Filter Paper Comparative Example 1-1 Unprocessed Paper ++ Example 1-2 Processed Fabric Comparative Example 1-2 Unprocessed Fabric Example 3 1 Processed synthetic leather Example 3-2 Comparative Example 3 Unprocessed synthetic leather ++ Example 4·1 Processed fabric (PET Tricot) Example 4-2 - Comparative Example 4 Processed fabric (no anti-allergic agent, PET Tricot) • H- (Evaluation) It is understood that Examples 1-1, 1_2, 3-1, 3-2, 4-1, and 4-2 contain the composition of the present invention, so that processing paper and processing excellent in anti-allergic properties are obtained. Cloth, processed synthetic leather. On the other hand, Comparative Example 3 does not contain as an anti-allergic agent. The results of the anti-allergic test were inferior to those of Examples 3-1 and 3-2. Further, it was found that Comparative Example 4 contained 2-(4-β-Sermyl)_iH-benzimidazole, 1H-2- Benzimidazolamide-based methyl decanoate and Thiabendazole, but not containing zirconia as an anti-allergic agent, are therefore less resistant to allergies than Examples 4-1 and 4-2. In order to confirm the durability improvement effect of the crosslinking agent, the PET 100% Tricot fabric of Examples 4-1, 4-2 and Comparative Example 4 was subjected to a predetermined number of household washing treatments in accordance with JIS 0217-103. (JIS [ 0217_ 103 : Household washing conditions). Adding a temperature of 4 〇χ: water to a household washing machine suitable for the above JIS standard, adding a synthetic lotion for clothing to a ratio of 2 g with respect to 1 L of water, 152257 .doc • 41 - 201138627 Dissolve it into a washing liquid. Put the sample and the required load cloth into the washing liquid at a bath ratio of 1:30, and start the operation. After 5 minutes of treatment, stop the operation and use the dehydrator. Dewatering the sample and the load cloth, and then changing the washing liquid to a new water at room temperature, in the same bath ratio After washing for 2 minutes, the mixture was washed for 2 minutes, dehydrated, and dried without being exposed to direct sunlight. Thereafter, the PET 100% Tricot fabric of Example 4-1, Example 4-2, and Comparative Example 4 was subjected to antibacterial treatment. Test, mold resistance test, aphid inhibition test, anti-allergen test. The results are shown in Tables 22 and 23. Further, in Tables 22 and 23, 10HL indicates the case where the home washing was performed 10 times, and 30HL indicates the case where the home washing was performed 30 times. [Table 22] Antibacterial test Antifungal performance test Sterilization activity 'ft value (Staphylococcus aureus) Evaluation of 5 grades after 4 encounters 10HL 30HL Initial 10HL 30HL Example 4-1 > 1.5 0.7 -0.1 0 0~ 1 2 Example 4-2 > 1.5 > 1.5 > 1.5 0 0 0 Comparative Example 4 - 1.0 - 1.2 - 1.2 4 4 4 [Table 23] Aphid inhibition test Anti-allergic test Proliferation inhibition rate (%) Mighty Checker Initial 10HL 30HL Initial 10HL 30HL Example 4-1 >99.9 90.0 70 - 士 + Example 4-2 >99.9 >99.9 97.3 _ - Comparative Example 4 - - - ++ ++ -H- (Evaluation) 152257.doc -42- 201138627 It is known that Example 4-2 contains a crosslinking agent in addition to the composition of the present invention, so that even if it is washed 30 times or more, it maintains antibacterial, antifungal, anti-mite, anti-allergy. Sex. On the other hand, it was found that Example 4·1 which does not contain a crosslinking agent has no antibacterial property, mold resistance, cochlear resistance, and antiallergic property as compared with Example 4-2. Further, in Comparative Example 4, although it contains 2·(4·thiazolyl)_1Η_benzimidazole, 1Η-2-benzoimidazolium carboxylic acid decyl ester, and rot, but does not contain an oxidizing port, it is known that for comparison Example 4, antibacterial, anti-mite, anti-mite, anti-allergic when washing more than twice, less than Example 1, 4-2 ° 152257.doc • 43-

Claims (1)

201138627 七、申請專利範圍: 1 · 一種組合物,其含有·· 3有選自咪唑系之有機系抗菌劑中之至少2種抗菌劑 的抗菌性組合物、 與過敏誘發物質之去活化劑。 2·如請求们之組合物,其中上述咪㈣之有機系抗菌劑 $具有苯并味唾環及嗟唾基之化合物、與具有苯并味嗤 環及胺基甲酸酯基之化合物。 3. 如租求項丨之組合物,其含有無機系抗菌劑。 4. 如請求項3之組合物,其中卜冰&— 兵1P上逑無機系抗菌劑為載銀填 酸錯。 5.如請求項1之組合物,其含有除蟎蟲劑。 6_如s青求項5之組合物,豆中卜a ,、甲上述除蜗蟲劑為氧化 有其之玻璃質。 7·如請求項1之組合物,其中上诚矾M# 丄返過敏誘發物質之去活“ 劑為源自天然之多酚類、合忐古 ㈣頰。成冋分子酚、及無機固體越 中之至少任'一種。 8. -種抗菌性處理劑’其含有如請求項R組合物、與分 散介質。 〃 9. 如請求項8之抗菌性處理劑’其含有黏合樹脂。 1〇·如請求項8之抗菌性處理劑,其含有交聯劑。 11.如請求項8之抗菌性處理劑,其 六T上述抗菌性處理劑g 生活用喷霧劑、塗料、塗布劑、 理劑中之任+ 纟面處理劑、及編 152257.doc 201138627 12. 一種抗菌性成形品 之抗菌性處理劑, 帛積層於樹脂膜上 成者。 ’其係利用如請求項8至11中任一項 對纖維、布拿、樹脂膜、將纖維或布 而成之積層體中之任一種進行處理而 13. 152257.doc 201138627 四、指定代表圖: (一) 本案指定代表圖為:(無) (二) 本代表圖之元件符號簡單說明: 五、本案若有化學式時,請揭示最能顯示發明特徵的化學式: (無) 152257.doc201138627 VII. Patent Application Range: 1 . A composition comprising: an antibacterial composition having at least two antibacterial agents selected from the group consisting of imidazole-based organic antibacterial agents, and a deactivating agent for an allergy-inducing substance. 2. The composition of the present invention, wherein the organic antimicrobial agent of the above-mentioned (4) has a compound having a benzo-salt ring and an anthracene group, and a compound having a benzo-oxime ring and a urethane group. 3. The composition of the claim , contains an inorganic antibacterial agent. 4. The composition of claim 3, wherein the inorganic antibacterial agent of the blister & bing 1P is silver-loaded. 5. The composition of claim 1 which comprises an insecticide. 6_ such as the composition of the smudge item 5, the beans in the a, A, the above-mentioned worms are oxidized and have their vitreous. 7. The composition of claim 1, wherein the above-mentioned decommissioning of the allergic-inducing substance is carried out by the "Mr. 矾M#", which is derived from natural polyphenols, 忐 忐 (4) cheeks, phenolic phenols, and inorganic solids At least one of the following: 8. An antibacterial treatment agent which contains the composition of claim R and a dispersion medium. 〃 9. The antibacterial treatment agent of claim 8 which contains a binder resin. The antibacterial treatment agent according to claim 8, which comprises a crosslinking agent. 11. The antibacterial treatment agent according to claim 8, wherein the six antibacterial treatment agent of the above-mentioned antibacterial treatment agent g, a paint, a coating agent, a physiotherapy agent任任任+ 纟面处理剂, and ed. 152257.doc 201138627 12. An antibacterial treatment agent for an antibacterial molded article, which is formed by depositing a layer on a resin film. The item is treated with any one of a fiber, a cloth, a resin film, and a laminate of fibers or cloth. 13. 152257.doc 201138627 IV. Designated representative drawings: (1) The representative representative of the case is: (none) (2) A brief description of the symbol of the representative figure: When the case if the formula, please reveal the best features of the invention show a chemical formula: (None) 152257.doc
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