JPS59163477A - Anti-bacterial and deodorizing processing of fiber article - Google Patents

Anti-bacterial and deodorizing processing of fiber article

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Publication number
JPS59163477A
JPS59163477A JP3413083A JP3413083A JPS59163477A JP S59163477 A JPS59163477 A JP S59163477A JP 3413083 A JP3413083 A JP 3413083A JP 3413083 A JP3413083 A JP 3413083A JP S59163477 A JPS59163477 A JP S59163477A
Authority
JP
Japan
Prior art keywords
monoglyceride
antibacterial
acid
water
bacterial
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP3413083A
Other languages
Japanese (ja)
Inventor
公雄 鈴木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Osaka Kasei Co Ltd
Original Assignee
Osaka Kasei Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Osaka Kasei Co Ltd filed Critical Osaka Kasei Co Ltd
Priority to JP3413083A priority Critical patent/JPS59163477A/en
Publication of JPS59163477A publication Critical patent/JPS59163477A/en
Pending legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は繊維製品の抗菌防臭加工法、更に詳しくは飽和
脂肪酸のモノグリセライド含有液で処理することにより
、褪維製品に抗1債防兵幼果を持1こせろ方法に関する
[Detailed Description of the Invention] The present invention provides an antibacterial and deodorizing processing method for textile products, and more specifically a method for imparting anti-1 bond young fruit to unfavorable textile products by treating them with a liquid containing monoglyceride of saturated fatty acids. Regarding.

靴F、肌看、スポーツ用衣服等は着用者の皮膚よりの分
泌物、汗、皮膚の剥離物等か付着し、これらが栄誉源と
なって細−等が増殖1−る良好な培地となり、細菌等の
産生物によって不快臭を発生し、場合によっては皮層病
等の感染原因ともなる。
Shoes, skin care products, sports clothing, etc. have secretions from the wearer's skin, sweat, skin peelings, etc. attached to them, and these serve as a source of glory and serve as a good medium for the growth of fine particles. , products such as bacteria generate unpleasant odors, and in some cases may cause infections such as skin disease.

この対策として近年繊維製品に抗菌性を持たせて皮屑面
及び繊維面の細菌等の増殖を迎えるとともに不快某発生
乞防止する、いわゆる衛生加工法が研究され、鋼等の金
属化合物、第7級アンモニウム塩やハロゲン含有物質等
、裡々の殺菌剤の使用が提案されている。しかし従来の
方法は抗e但スペクトルが不十分でおつ1こり、人体に
対して毒性が1;虫かったり、或トま皮ノ))に対し例
数性があったり、異臭があったり、日光に当ると次第に
処理物を変色又はン6已さ、芦たり、洗たく、漂白処理
又はアニオン系界面活性剤や金属塩等との作用にエリ変
質又は変色或は効力が著しく滅失したり、処理すること
IK、より繊維の本来の物性を損ったり(例えば吸水性
をなくして覆水性に変えたり、柔軟性を損ったり)或は
抗菌力保持期間延長のための処理(例えば樹脂加工処理
、固着力増強のための官能基付加等)Vt−Xり本来の
抗菌力が抑制されて十分な効果が発揮されなかったりし
て、実際に満足できる抗菌防臭加工法は容易に得られ難
い状況である。
As a countermeasure against this problem, research has been conducted in recent years on so-called hygienic processing methods, which provide antibacterial properties to textile products to prevent the proliferation of bacteria on the skin and fiber surfaces, as well as to prevent the occurrence of certain discomfort. The use of local disinfectants, such as grade ammonium salts and halogen-containing substances, has been proposed. However, the conventional methods have insufficient anti-emission spectra, are toxic to the human body, are susceptible to insects, tomato skin, etc., and have a strange odor. When exposed to sunlight, the treated product may gradually change color or become stale, or may deteriorate or lose its effectiveness significantly due to drying, washing, bleaching treatment, or the action of anionic surfactants, metal salts, etc. Treatments that impair the original physical properties of the fibers (e.g., eliminate water absorption and make them water-repellent, or impair flexibility) or treatments to extend the period of antibacterial activity (e.g., resin treatment) treatment, addition of functional groups to enhance adhesion, etc.) Vt-X's original antibacterial power may be suppressed and sufficient effects may not be exhibited, making it difficult to obtain an actually satisfactory antibacterial and deodorizing processing method. It's a situation.

本発明者は安全で且つ効果の優れた繊維の衛生加工法の
開発を目的として検討を重ね、飽和脂肪酸のモノグリセ
ライドが繊維に対して親和力が強< −(*、維の物性
に悪影智乞全く与えず、耐光性もよく、通常の繊維処理
条件では化学的に安定であり且つ十分な抗菌力を示すこ
とを見い出し、強力でしかも極めて安全な繊維の抗菌防
臭加工法を確立するに至ったものである。
The present inventor has conducted repeated studies with the aim of developing a safe and highly effective hygienic processing method for fibers, and has found that monoglycerides of saturated fatty acids have a strong affinity for fibers. We discovered that it does not have any harmful effects, has good light resistance, is chemically stable under normal fiber processing conditions, and exhibits sufficient antibacterial activity, leading to the establishment of a strong yet extremely safe antibacterial and deodorizing processing method for fibers. It is something.

脂肪酸モノグリセライドは乳化、分散、乳化安定剤等の
目的で食品に広く用いられ、油脂の人体内の代謝物であ
ることから特に安全性は亮<iif@Iiされているも
のであり、反虜刺畝性もみられない。炭素数6〜Igの
脂肪酸のモノグリセライドは抗菌力があり特に炭素数ざ
ヘー/、2の脂肪酸のモノグリセライドは抗菌力が強く
、食品及び化粧品の分野で保存剤として応1月すること
は既に知られている。
Fatty acid monoglycerides are widely used in foods for the purposes of emulsification, dispersion, emulsion stabilizers, etc., and because they are metabolites of fats and oils in the human body, their safety is particularly high. No ridges are seen. Monoglycerides of fatty acids with a carbon number of 6 to Ig have antibacterial properties, and monoglycerides of fatty acids with a carbon number of 2 to 2 have particularly strong antibacterial properties, and it is already known that they can be used as preservatives in the fields of food and cosmetics. ing.

本発明方法に使用される脂肪酸のモノグリセライドとし
て(ま鍾々のものを使用し得ろρ・、抗菌力、取扱い易
さ等を考慮すると、通′市炭素叔6〜Ig、特に炭紫峨
g〜/−の直鎖の飽和脂肪酸のモノグリセライドが好ま
しい。具体的lではカグリル酸、カプリン酸、ラウリル
酸、ミリスチン酸、パルミチン酸、ステアリン酸等のモ
ノグリセライドか入手容易で、好互しぐ使用される。
As the monoglyceride of fatty acids used in the method of the present invention, considering the antibacterial activity, ease of handling, etc., it is recommended to use monoglycerides of fatty acids (Tong'shi Gansu 6-Ig, especially charcoal-based monoglycerides). Monoglycerides of straight chain saturated fatty acids of /- are preferred.Specifically, monoglycerides such as cargyrylic acid, capric acid, lauric acid, myristic acid, palmitic acid, and stearic acid are easily available and are preferably used interchangeably.

Ha u 峻モノグリセライドの市販品はジグリセライ
ド等を不純物として含むのか通nであるが、不純物が増
加すると抗菌力低下か太きいためモノグリセライド“の
純度か7θd【M′%以上、好ましぐ’t’i ?θ重
量擺以上のものか適している。なお必要によってはイセ
の過当な殺菌剤と併用して効果の増強を図ることを妨け
るものではない。
Commercially available monoglyceride products contain impurities such as diglycerides, but as impurities increase, the antibacterial activity decreases or becomes thicker, so the purity of the monoglyceride must be 7θd[M'% or higher, preferably 't'. It is suitable if it has a weight of more than i?θ.However, if necessary, this does not preclude using it in combination with an appropriate fungicide to enhance the effect.

本発明の処理方法の本′AはS:紅製品に脂肪酸モノク
リセライトを浸這、同所させろことであり、その手段と
してに例えは脂肪酸モノグリセンイドを水に乳化又は可
溶化させた液(処理歳)に常温又は加温下に繊維製品を
浸偵し次いで絞り、乾汗工程をべろ方法或は繊維製品に
処理液を噴霧又は塗布した佼乾蔗する方法等がある。
The main point of the treatment method of the present invention is to infiltrate fatty acid monoglycerite into the red product and apply it to the same place. There are methods such as soaking the textile product at room temperature or under heating, then squeezing it, and drying it by drying, or spraying or coating the textile product with a treatment solution.

なお処理7反は水以夕tに低θ1点の有機溶媒(例えば
メタノール、アセトン、ジクロルメタン等)の浴液等を
用いることもできろ。J猶肋1蚊モノグリセライドはそ
れ自体水中に乳化する能力を成程度持っており、通常、
水中で一度加温(ム崗(通常融点が常温以上なので)さ
せた後j;eゼ1ミすると不完全ながら白ン蜀乳化状悪
とすることができる。しかしこの場合、凝固点より約1
0′c以−ヒ温朋が低下才ろと倣細な結晶が析出し、更
に昌度が低下してゆくと分離沈でんしてし1つ。
For the treatment, a bath solution of an organic solvent having a low θ1 point (for example, methanol, acetone, dichloromethane, etc.) may be used instead of water. Mosquito monoglyceride itself has a certain ability to emulsify in water, and usually
After heating (normally the melting point is above room temperature) in water, it is possible to form a white emulsion, albeit incompletely, by heating it for 1 minute.
As the temperature decreases from 0'C onwards, fine crystals precipitate out, and as the temperature decreases further, they separate and precipitate.

従って本発明方法に於ては、脂肪酸モノクリセライトと
界面活性剤とハイドロトロープ(有戦物質の水−乳化剤
系の中での溶解性を促進1−ろ物質;特開昭り9−37
577号参照)とを目己合して調製した濃厚液を水で希
釈して安定な!し化液又は可溶化液を用いて繊維製品を
処1ffi ’1”ることが好ましい。
Therefore, in the method of the present invention, fatty acid monochrycerite, a surfactant and a hydrotrope (1-filter substance that promotes the solubility of the active substance in a water-emulsifier system; JP-A-9-37
577)) and dilute it with water to make it stable! Preferably, the textile product is treated using a curing solution or a solubilizing solution.

界面活性剤としては、アニオン系、非イオン系、両a系
の各独のものを/種又トユ2神辺上混合して用いること
ができろ。例えQ71−アルキルアリルスルホン愼塩、
ポリオキシエチレンアルキル71Jルエーテル硫岐塩、
ポリオA・ジエチレンアルキルニーデル硫酸塩、ジアル
キルスルホザクシネ−ト、ポリオキシエチレンアルキル
エーテル、ポリオキシエチレンアルキルアリルエーテル
、ポリオキシエチレン並11)j 酸エステル、ンルヒ
タン崩肪峻ニスデル、ポリオキシエテレンソルヒタンハ
i′i ILう敬エステル、ショ砧脂肋微エステル、ア
ルキルグリシン、アル千ルベタイン等が春けられろ。
As the surfactant, anionic, nonionic, and both a-type surfactants can be used in combination. For example, Q71-alkylaryl sulfone salt,
Polyoxyethylene alkyl 71J ether sulfur salt,
Polio A/diethylene alkyl needle sulfate, dialkyl sulfosuccinate, polyoxyethylene alkyl ether, polyoxyethylene alkyl allyl ether, polyoxyethylene 11)j acid ester, nysdel ester, polyoxyethylene Solhitanha i'i IL esters, alkylglycines, alkylglycines, alkylbetaines, etc. should be used in the spring.

このハイドロトロープとしてし1一般に凡用されろもの
をl不でu又シエユ僚り上群合して1月いられる。例え
はメタノール、エタノール1.− (及ヒlso −)
プロパツール、メチルエチルケトン、メチルn−(及び
1so−)プロピルケトン、エチレンクリコール、フロ
ピレンクリコール、トリエタノールアミン、エチレンク
リコ〜ル七ノ5−アルキル(以下アルキルと称するのは
メチル、エチル、フロビル、メチル’& 指f)エーテ
ル、プロピレンクリコールモノアルキルエーテル、ジエ
チレングリコールモノアルキルエーテル、シグロビレン
クリコールモノアルキルエーテル、3−メチル−3−メ
トキシブタノール、N−メチル−ニーピロリドン等が挙
げられろ。
As this hydrotrope, it is possible to combine commonly used materials into a variety of species. For example, methanol, ethanol 1. - (and Hi lso -)
propatool, methyl ethyl ketone, methyl n-(and 1so-)propyl ketone, ethylene glycol, propylene glycol, triethanolamine, ethylene glycol 7-5-alkyl (hereinafter alkyl refers to methyl, ethyl, furovir) , methyl'& f) ether, propylene glycol monoalkyl ether, diethylene glycol monoalkyl ether, siglobylene glycol monoalkyl ether, 3-methyl-3-methoxybutanol, N-methyl-nipyrrolidone, and the like.

脂肪酸モノグリセライドの濃厚液な惹製する界面活性H
]1o、 o o t〜、20、ハイドロトロープ(ア
ルコール類’;<除<)o、oot〜夕0、アルコール
類θ〜所定希釈一度の範囲が好〜ましい。
Surface active H that attracts concentrated liquid of fatty acid monoglyceride
] 1 o, o o t~, 20, hydrotrope (alcohol';<excluding<) o, oot~e 0, alcohol θ~a predetermined dilution once.

更に必要に応じて適当型の水を加えて痘朋を調整するこ
とができろ。
Furthermore, if necessary, you can adjust the pox by adding an appropriate type of water.

脂肪酸モノグリセライドの処理量は対象とする繊維製品
の種類や用途により異なり、広(・範囲から辿ばれるが
、通常繊維製品の乾妹血(dに対し、0.0/〜左循の
処理で長期間抗菌防臭力をも′1″る繊維製品が得られ
る。
The amount of fatty acid monoglyceride processed varies depending on the type and purpose of the target textile product, and can be traced from a wide range. A textile product that also has antibacterial and deodorizing properties for a long time can be obtained.

脂肪酸モノクリセライトは木綿繊kf+; lL対して
特VC強い親和カビ千4も30回以上の洗1こく後も十
分な抗菌力を持続する。他の天然又l′i合成のは維に
ついても有効で少くとも数回以上の洗たく耐久性を持つ
ことが認められた。この性能は#i2維に対する合成側
面加工(例えはアクIJ /l/系、ウレタン系等の合
成樹脂エマルジョンによる繊維の処理)を併用すること
により、さらに向上させることができる。
Fatty acid monochrycerite has a special VC affinity for cotton fibers, and maintains sufficient antibacterial activity even after washing for more than 30 times. It has been found that other natural or l'i synthetic fibers are also effective and durable for at least several washes. This performance can be further improved by concurrently applying a synthetic side surface treatment to the #i2 fibers (for example, treatment of the fibers with a synthetic resin emulsion such as Aku IJ /l/ type, urethane type, etc.).

本発明の方法で処理され1こ抗菌加工稙f、(4,製品
は、本処理薬品に起因する本来のj諷維の物性の悪化例
えば柔軟性の減少、撥水性の発見1、日光照射による量
化、=ik光漂白剤との反応や化学漂白剤等の作用によ
る変質、変色等は通常便用する榮件では全く起らない。
The product treated with the method of the present invention has been treated with antibacterial processing (4).The product has been treated with deterioration of the physical properties of the original fiber due to the treatment chemicals, such as a decrease in flexibility, and the discovery of water repellency (1) due to sunlight irradiation. Quantification, = ik Deterioration, discoloration, etc. due to reaction with photobleaching agents or the action of chemical bleaching agents, etc. do not occur at all under normal circumstances.

また、後記英施例からす」らかな呼に、本発明方法で処
理されTこ繊維製品は各種細菌、真菌に対し長期に亘り
十分な抗菌力を示す。壕だ)前肋殴モノグリセライドが
食品添加物として認められていることからも明らかな様
に安全性も医れている。
In addition, as shown in the Examples below, the fiber products treated by the method of the present invention exhibit sufficient antibacterial activity against various bacteria and fungi over a long period of time. It is also safe, as evidenced by the fact that monoglyceride is approved as a food additive.

次に実施例を4′・けて本発明方法を具体的に説つ」す
るが、本発明はこれらの実施例に限定されるものではな
い。なおφは%に言己載のない限り重量%を示す。
Next, the method of the present invention will be specifically explained with reference to Examples, but the present invention is not limited to these Examples. Note that φ indicates weight % unless otherwise stated.

実施例/ 原液基本処方 脂肪l竣モノグリセライド         30%N
a・ボlJiシw5−vyノニルフェニルニーテア1/
シルフェート(ポヅ効〃数/θ)   5% 一カ ジフロピレングリコールモノフチルエ−7/+7/  
5  %メタノール          30%水  
                      20 
%原液基本処方において脂肪酸モノクリセライトとして
次のものな使用し、それぞれの原液をs、’、+ 4す
した。
Example / Stock solution basic prescription fat monoglyceride 30%N
a・boljishi w5-vy nonylphenylnitea 1/
Sylphate (potency number/θ) 5% 1-Kadifuropylene glycol monophthyl ether 7/+7/
5% methanol 30% water
20
% stock solution In the basic recipe, the following fatty acid monochrycerite was used, and each stock solution was sipped by s, ', +4.

反射、/°カプリル暇モノグリセライド(純度約り0%
)原#!:2:カグリン峨モノグリセライド(縄匿約q
O%)原券、3:ラウリン酸モノグリセライド(純度約
90%)原液μ″原敢、2.3の等掘−混合物 原液5°カプロン酸、カプリル岐(A)、カプリン酸(
B)、ラウリン酸(C)、ミリスチン岐、バルミチン峻
、ステアリン改の各モノグリセンイドの混合吻(A+B
+Cは約7θ%) 各原液を水で布状して所定の#度とした。次Ic h+
メリヤス布地ηにこの液に浸σよ後直らに約/g倍重量
に絞り乾燥しブこ。各試験布はJIS L−10/g(
H法)により30回の洗たく?行い、るヒたく耐久性の
砥料とした。
Reflection, /° Caprylic monoglyceride (purity approximately 0%)
)original#! :2:Kagrin monoglyceride
O%) Original note, 3: Lauric acid monoglyceride (purity approximately 90%) stock solution μ'' Gengan, 2.3 equal dilution - mixture stock solution 5° Caproic acid, Caprylic acid (A), Capric acid (
B), mixed proboscis of lauric acid (C), myristic acid, valmitin, and stearin modified monoglycenoids (A+B
+C is about 7θ%) Each stock solution was made into a cloth with water to a predetermined degree. Next Ic h+
After soaking the knitted fabric in this solution, it was immediately squeezed to about 1/g/g weight and dried. Each test cloth is JIS L-10/g (
Wash 30 times using method H)? It was made into a highly durable abrasive.

抗=を試験1去′l工直径ご3 crnの滅1豹シャー
レ中に/ !i 7n!、の寒天億地(細菌の場合は一
#通刃こ大培地馨、真菌の場合(まPDA培地を使用し
た。)を注入後固化させ、その上に上記の試J検浦を/
×2(7nVC裁断して鴎床した。試験布及び培地全面
に下記の供試菌の懸濁液/ mlを接種しγこ後、シτ
−レケ転倒させて細1(す37CIIg時1司、真菌は
3θcio日間培養を行い試;茨イ1j周Hの阻止円径
又は試1験布上での田の生角゛の有無、面積を調査した
The anti-resistance test is carried out in a leopard petri dish. i7n! Inject and solidify agar agar (for bacteria, PDA medium was used), and then add the above test sample on top of it.
×2 (7nVC cut and molded) A suspension of the following test bacteria/ml was inoculated on the test cloth and the entire surface of the medium.
- Test by inverting the rack and culturing the fungus for 3θcio days. investigated.

なお既市販品の抗困加工組下、2種(Ta製及供試細i
 : S、aureus、B、 aubtilis、E
、 colt37℃2q時間前培養ヲ行っ時間前培養上
行らl工−ゼゲ釣(′4し一〇mll t))殺菌水中
圧悪淑さ供試真i4 : T、 mcntagroph
ytes3007〜10日前培養ケ行ったスラント」ニ
ノ からlエーゼをとり乳鉢中で磨砕後20 tnl O)
収態水中に眉宕蜀させて使用し1こ。
In addition, there are two types of commercially available products with anti-difficulty processing (Ta made and sample type I).
: S, aureus, B, aubtilis, E
, Colt 37℃ 2 q hour pre-incubation, 1 hour pre-incubation, 10 ml t)) Sterilization water pressure test True I4: T, mcntagroph
ytes3007 ~ 10 days ago cultured slant was taken from Nino and ground in a mortar for 20 tnl O)
Use 1 bottle of eyebrows in water.

試、験結果を表1に示す。The test results are shown in Table 1.

表  l カヒ抵仇性1lIt)工〔l〕:試験片の5以上で生首
、〔ユ〕:試験片の%以下で生角、〔3〕:試験片、1
:に生胃を認めな(−0 雑困付着:他の雑菌が住官して2I(」定不能。
Table l Kahī resistance 1lIt) Work [l]: 5 or more of the test piece is a dead neck, [Y]: % or less of the test piece is a dead horn, [3]: A test piece, 1
: Do not allow raw stomach (-0) Miscellaneous adhesion: Other germs may be present (2I) (Undetermined).

※ 領水性か強い。* Strong territorial nature.

実施例λ アクリル繊維布地を用いて実施例1の方法に準じて抗菌
効果を試験した。
Example λ The antibacterial effect was tested according to the method of Example 1 using acrylic fiber fabric.

3及びグの試験では試験薬剤にアクリル系樹脂エマルジ
ョンヲ9%添加して処理した。結果は表コに示す。
In tests 3 and 3, 9% acrylic resin emulsion was added to the test agent. The results are shown in the table.

表  コ 実施例3 実施例1において原液(4)の20倍液で処理後JIS
 L−10/g  の方法で30回洗Tこくした綿メリ
ヤス布地を次亜塩素酸ナトリウム浴液(活性塩素02%
)に常温で30分浸び4した抜、水洗乾燥し、次亜塩素
酸ナトリウム処理前と後の抗菌効力を比較した。結果を
表3に示す。
Table Co Example 3 JIS after treatment with 20 times the stock solution (4) in Example 1
A cotton knitted fabric that has been washed 30 times using the method of L-10/g is soaked in a sodium hypochlorite bath solution (active chlorine 02%).
) for 30 minutes at room temperature, rinsed with water, dried, and compared the antibacterial efficacy before and after treatment with sodium hypochlorite. The results are shown in Table 3.

表 3 実施例q 実施例/で使用した脂肪酸モノグリセライド処理した純
メリヤス両面(螢光漂白剤処理)布地を日光に/カ月間
曝蕗し色調の変化を親類した。同時にモノグリセライド
処理をしブ、Cい同じ布地について比奴試験をし1こ。
Table 3 Example q The fatty acid monoglyceride-treated pure knitted double-sided fabric (fluorescent bleach treated) used in Example 1 was exposed to sunlight for a month to observe changes in color tone. At the same time, a monoglyceride treatment was performed on the same fabric, and a comparison test was conducted.

結果は処理布と未処理布とは全く同等で、量化、変色は
認められなかった。
The results were completely the same for the treated and untreated fabrics, with no quantification or discoloration observed.

実施例S A液 カプリル酸とカプリン酸σつ各モノグリセライド
の等量混合物1O9−をエタノール20グ・にとかす。
Example S Solution A A mixture of equal amounts of caprylic acid and capric acid σ monoglycerides (109−) is dissolved in 20 g of ethanol.

この溶液二Ofをグ0℃の水q、gotlに混合し均一
にし1こ。
Mix this solution with water at 0°C and make it homogeneous.

B液 ラウリン懐モノグリセライド/79−r7エタノ
ール999−に溶解した。
Solution B: Laurin monoglyceride/79-r7 was dissolved in 999% of ethanol.

イ、靴下(アクリル、ポリエステル、ナイロン、毛の混
紡)1足の片足分をAFLに浸演し1丁1ちに絞って重
量ケ無処理物の25倍とし、これをノ虱乾し1こ。(モ
ノグリセライド付着量は靴下重量の7%) 口、イと同等の靴下の片足分に靴下重量と等重量のB液
を悠抽付着させた後、風乾した・(モノグリセライド付
着量は靴下庫%H)7%)イ及び口の処理をした靴下を
未処理の片足分とl対にして各3足分ずつ用意し、それ
ぞれ7日間着用後洗たく、乾燥を3回経返した後q回目
にa日間続けてNI:l:1シて臭いを比較しTこ。な
お靴は新品の運動靴′ff:用い試1荻前力・らσ)着
臭σ)影響なり1い1ξ。結果は表グに示す。
B. Dip one pair of socks (acrylic, polyester, nylon, wool blend) into AFL, squeeze each sock to make it 25 times the weight of untreated socks, and dry it with lice. . (The amount of monoglyceride adhered is 7% of the sock weight.) After applying liquid B in an amount equal to the weight of the sock to one leg of a sock, the amount of monoglyceride adhered was 7% of the sock weight. ) 7%) Prepare 3 pairs of each pair of treated socks with one pair of untreated socks, wear them for 7 days, wash them, dry them 3 times, and then dry them for the qth time. Compare the odor using NI:L:1 for several days in a row. The shoes were new athletic shoes. The results are shown in Table G.

表  ゲ 甘 飾い不快臭 十 駒い不快臭 −不快臭なし 出縁1人 大阪化成株式会社 代理人  弁理士 長谷用   −:′−□′〕湯  
  ブ1 ほか7名 −゛−
1 person with no unpleasant odor - Osaka Kasei Co., Ltd. agent Patent attorney Hase -:'-□'〕Yuyu
B1 and 7 others −゛−

Claims (2)

【特許請求の範囲】[Claims] (1)飽和脂肪酸のモノグリセライド含有液を用いて繊
維製品を処理することを特徴とする繊維製品の抗菌防臭
加工法
(1) Antibacterial and deodorizing processing method for textile products, characterized by treating the textile products using a liquid containing monoglyceride of saturated fatty acids
(2)炭素数g−/2の飽和脂肪酸のモノグリセライド
を1史用することを71?−偵とする特許請求の範囲第
1項記載の繊維製品の抗菌防臭加工法
(2) Is it 71 to use monoglyceride of saturated fatty acid with carbon number g-/2? - Antibacterial and deodorizing processing method for textile products as claimed in claim 1
JP3413083A 1983-03-02 1983-03-02 Anti-bacterial and deodorizing processing of fiber article Pending JPS59163477A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3413083A JPS59163477A (en) 1983-03-02 1983-03-02 Anti-bacterial and deodorizing processing of fiber article

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3413083A JPS59163477A (en) 1983-03-02 1983-03-02 Anti-bacterial and deodorizing processing of fiber article

Publications (1)

Publication Number Publication Date
JPS59163477A true JPS59163477A (en) 1984-09-14

Family

ID=12405642

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3413083A Pending JPS59163477A (en) 1983-03-02 1983-03-02 Anti-bacterial and deodorizing processing of fiber article

Country Status (1)

Country Link
JP (1) JPS59163477A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6762339B1 (en) 1999-05-21 2004-07-13 3M Innovative Properties Company Hydrophilic polypropylene fibers having antimicrobial activity
US9777407B2 (en) 2009-03-27 2017-10-03 3M Innovative Properties Company Hydrophilic polyproylene melt additives
US9826770B2 (en) 2005-03-10 2017-11-28 3M Innovative Properties Company Antimicrobial compositions comprising esters of hydroxycarboxylic acids
US10471036B2 (en) 2003-09-09 2019-11-12 3M Innovative Properties Company Antimicrobial compositions and methods
US20200017665A1 (en) * 2018-07-10 2020-01-16 Nano And Advanced Materials Institute Limited Germ-repellent material
US10918618B2 (en) 2005-03-10 2021-02-16 3M Innovative Properties Company Methods of reducing microbial contamination

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57205513A (en) * 1981-06-05 1982-12-16 Asahi Chem Ind Co Ltd Treating method of copper-ammonia cellulosic fiber

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57205513A (en) * 1981-06-05 1982-12-16 Asahi Chem Ind Co Ltd Treating method of copper-ammonia cellulosic fiber

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6762339B1 (en) 1999-05-21 2004-07-13 3M Innovative Properties Company Hydrophilic polypropylene fibers having antimicrobial activity
US10471036B2 (en) 2003-09-09 2019-11-12 3M Innovative Properties Company Antimicrobial compositions and methods
US9826770B2 (en) 2005-03-10 2017-11-28 3M Innovative Properties Company Antimicrobial compositions comprising esters of hydroxycarboxylic acids
US10918618B2 (en) 2005-03-10 2021-02-16 3M Innovative Properties Company Methods of reducing microbial contamination
US9777407B2 (en) 2009-03-27 2017-10-03 3M Innovative Properties Company Hydrophilic polyproylene melt additives
US20200017665A1 (en) * 2018-07-10 2020-01-16 Nano And Advanced Materials Institute Limited Germ-repellent material

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