JPS642707B2 - - Google Patents

Info

Publication number
JPS642707B2
JPS642707B2 JP9219981A JP9219981A JPS642707B2 JP S642707 B2 JPS642707 B2 JP S642707B2 JP 9219981 A JP9219981 A JP 9219981A JP 9219981 A JP9219981 A JP 9219981A JP S642707 B2 JPS642707 B2 JP S642707B2
Authority
JP
Japan
Prior art keywords
fibers
polyurethane
polyurethane fibers
polyester
melting point
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP9219981A
Other languages
Japanese (ja)
Other versions
JPS57210068A (en
Inventor
Shoji Takei
Yoshinori Morifuji
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP9219981A priority Critical patent/JPS57210068A/en
Publication of JPS57210068A publication Critical patent/JPS57210068A/en
Publication of JPS642707B2 publication Critical patent/JPS642707B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は防黴加工されたポリウレタン繊維の製
造法に係わるものであり、その目的は防黴剤の使
用量が少なく、かつ簡単な熱処理により着色、物
性低下なく耐久性良好な防黴性能をもつポリウレ
タン繊維を得ることにある。 ポリウレタン繊維はその弾性機能が他のあらゆ
る繊維に比べて特徴的であるため、各種の商品分
野において他の合成繊維、天然繊維と交編、交織
されて使用されてきた。現在市場に見られるポリ
ウレタン繊維は大きく分けると、その弾性機能を
つかさどる化学組成としてポリエーテルから成る
ものと、ポリエステルから成るものとがある。こ
のポリエステル系ポリウレタン繊維は、ポリエー
テル系のそれに比較して構成成分の選択が巾広く
弾性機能も設計し易い。又耐塩素脆化性、酸化劣
化に対する抵抗力も優れるので、ポリウレタン繊
維の特定の商品分野においてはその優位性を発揮
できるが、生活空間に存在するある種の黴、細
菌、バクテリア等の微生物によつて脆化し易いと
いう欠点をもつている。 このポリエステル系ポリウレタンを脆化させる
微生物は自然界に存在する特定種のものではある
が、一般にこれら繊維が使用される生活空間には
必ず存在していることは現実に脆化現象が再現さ
れることから確認できる。この微生物によつて脆
化したポリウレタン繊維はもはや弾性機能は全く
なくなり、商品価値は失なわれる。この様な欠点
を改善するためには一般に防黴剤と呼ばれる殺菌
性物質をポリウレタン繊維に付与すれば良いが、
防黴剤は一般に安全衛生上注意すべきものが多
く、特に肌着等に多く使用されるポリウレタン繊
維においては充分に配慮されねばならない問題で
ある。特に有機金属系の防黴剤はこの傾向が強く
避けねばならない。又、特にポリウレタン繊維
は、一般に薬剤処理により黄変、脆化し易いもの
であり、かかる観点からも防黴剤を付与するとい
う概念は採用しがたいものであつた。 本発明者らは、かゝる現状に鑑み、これらの欠
点を改善し、ポリエステル系ポリウレタン繊維か
ら成る繊維製品が不特定多数の消費者の手に渡つ
てからの洗濯繰返しによつても脆化の危険性のな
いポリウレタン繊維を製造する方法について鋭意
検討した結果、本発明を完成するに至つた。 即ち、本発明はポリウレタン繊維に防黴剤を有
機溶剤を含まない水分散液として付与した後、熱
処理することを特徴とする防黴加工されたポリウ
レタン繊維の製造法にある。 本発明者らは、ポリエステル系ポリウレタン繊
維に、無機性/有機性バランスが1.0以下で、か
つ融点又は分解点および分子量が下記式(1)、(2)、
(3)および(4)を同時に 7m+9M≧3150 −(1)、 5m+6M≦3600 −(2)、 m≧5 −(3)、 M≧100 −(4) 満足する防黴剤を付与し、熱処理することによ
り、極めて耐洗濯性に富む防黴性能を付与できる
事実を見い出したのである。(式中のmは融点又
は分解点(℃)、Mは分子量を表わす) 以下、本発明を更に詳しく説明する。 本発明のポリウレタン繊維の製造に用いられる
ポリエステルジオールは、エチレングリコール、
1,4−ブタンジオール、1,2−プロパンジオ
ール、ネオペンチレングリコール等のジオール類
の一種もしくはそれ以上のグリコールと、例えば
アジピン酸等のジカルボン酸の縮重合により得ら
れたもの、およびε−カプロラクタムの開環重合
によつて得られるものを含み、これらは単独もし
くは混合して用いても良い。 これらポリウレタン繊維は多くの実施形態とし
ては、アクリル、ポリアミド、ポリエステル繊維
等の合成繊維、再生セルロース繊維、あるいはウ
ール、綿等の天然繊維等と交撚、交編、交織され
ている。 本発明でいう防黴剤とは黴の生長、繁殖を抑制
するか死滅させる薬剤であり、有機水銀系化合
物、フエノール類およびその塩素化合物、ナフテ
ン酸等の有機酸の金属塩、第4級アンモニウム化
合物などがある。 本発明でいう無機性/有機性バランスとは界面
活性剤のH.L.B(Hydrophile−Lypophile
Balance:親水性親油性バランス)に相当するも
ので、藤田〔化学の領域、11巻、721頁、1957年、
南江堂〕によつて提唱されたものであり、有機化
合物の溶解度、融点、その他物理的性状、生理作
用などの指標となるものである。この概念によれ
ば、有機化合物の全性状は次式のごとく表わされ
る。
The present invention relates to a method for manufacturing anti-mildew treated polyurethane fibers, and its purpose is to use a small amount of anti-mildew agent and to have a durable anti-mildew property without coloring or deterioration of physical properties through simple heat treatment. The purpose is to obtain polyurethane fibers. Since polyurethane fibers have unique elastic properties compared to all other fibers, they have been used in a variety of product fields by being mixed or woven with other synthetic fibers or natural fibers. Polyurethane fibers currently available on the market can be roughly divided into two types: those made of polyether and those made of polyester, which have a chemical composition that controls their elasticity. Compared to polyether-based polyurethane fibers, this polyester-based polyurethane fiber has a wider selection of constituent components and is easier to design with its elastic function. In addition, it has excellent resistance to chlorine embrittlement and oxidative deterioration, so it can be used for certain product fields of polyurethane fibers, but it can be used against certain types of microorganisms such as mold, bacteria, and bacteria that exist in living spaces. It has the disadvantage of being easily embrittled. Although the microorganisms that cause this polyester-based polyurethane to become brittle are specific species that exist in nature, the fact that they are present in living spaces where these fibers are generally used means that the brittleness phenomenon can actually be reproduced. You can check from Polyurethane fibers that have become brittle due to these microorganisms no longer have any elastic function and lose their commercial value. In order to improve these defects, it is generally necessary to add a bactericidal substance called a fungicide to polyurethane fibers.
Generally speaking, there are many things that should be taken into account when it comes to antifungal agents from the standpoint of safety and health, and this is an issue that must be taken into consideration particularly when it comes to polyurethane fibers, which are often used in underwear and the like. In particular, organometallic antifungal agents have this tendency and must be avoided. In addition, polyurethane fibers in particular are generally susceptible to yellowing and becoming brittle when treated with chemicals, and from this point of view as well, it has been difficult to adopt the concept of adding a fungicide. In view of the current situation, the present inventors have attempted to improve these drawbacks and prevent textile products made from polyester-based polyurethane fibers from becoming brittle even after repeated washing after being handed over to an unspecified number of consumers. As a result of extensive research into a method for producing polyurethane fibers that does not pose any danger, the present invention has been completed. That is, the present invention resides in a method for producing mold-proofed polyurethane fibers, which comprises applying a mold-proofing agent to polyurethane fibers as an aqueous dispersion containing no organic solvent, and then heat-treating the polyurethane fibers. The present inventors have developed a polyester polyurethane fiber with an inorganic/organic balance of 1.0 or less, a melting point or decomposition point, and a molecular weight of the following formulas (1), (2),
(3) and (4) at the same time 7m+9M≧3150 −(1), 5m+6M≦3600 −(2), m≧5 −(3), M≧100 −(4) Apply a satisfying fungicide and heat treat By doing so, they discovered that it is possible to impart mold-proofing properties with extremely high wash resistance. (In the formula, m represents the melting point or decomposition point (°C), and M represents the molecular weight.) Hereinafter, the present invention will be explained in more detail. The polyester diol used in the production of the polyurethane fiber of the present invention is ethylene glycol,
Those obtained by condensation polymerization of one or more diols such as 1,4-butanediol, 1,2-propanediol, and neopentylene glycol and dicarboxylic acids such as adipic acid, and ε- These include those obtained by ring-opening polymerization of caprolactam, and these may be used alone or in combination. In many embodiments, these polyurethane fibers are twisted, knitted, or woven with synthetic fibers such as acrylic, polyamide, and polyester fibers, regenerated cellulose fibers, or natural fibers such as wool and cotton. The antifungal agent in the present invention is an agent that suppresses or kills the growth and reproduction of mold, and includes organic mercury compounds, phenols and their chlorine compounds, metal salts of organic acids such as naphthenic acid, and quaternary ammonium. There are compounds, etc. The inorganic/organic balance in the present invention refers to the surfactant HLB (Hydrophile-Lypophile).
Fujita [Chemistry, Vol. 11, p. 721, 1957]
[Nankodo], and serves as an indicator of the solubility, melting point, other physical properties, physiological effects, etc. of organic compounds. According to this concept, the overall properties of an organic compound can be expressed as shown in the following formula.

【表】 全分子 全分子 全分子
[Table] All molecules All molecules All molecules 〓

Claims (1)

【特許請求の範囲】 1 ポリウレタン繊維に防黴剤を有機溶剤を含ま
ない水分散液として付与した後、熱処理すること
を特徴とする防黴加工されたポリウレタン繊維の
製造法。 2 ポリウレタンの構成成分が、ポリエステルで
あることを特徴とする特許請求の範囲第1項記載
の製造法。 3 防黴剤の無機性/有機性バランスが1.0以下
で、かつ融点又は分解点および分子量が下記式
(1)、(2)、(3)および(4)を同時に満足することを特徴
とする特許請求の範囲第1項記載の製造法。 7m+9M≧3150 (1) 5m+6M≦3600 (2) m≧5 (3) M≧100 (4) 式中、mは融点又は分解点(℃)、Mは分子量
を表わす。
[Scope of Claims] 1. A method for producing anti-mildew-treated polyurethane fibers, which comprises applying an anti-mildew agent to polyurethane fibers as an aqueous dispersion containing no organic solvent, and then heat-treating the fibers. 2. The manufacturing method according to claim 1, wherein the constituent component of the polyurethane is polyester. 3 The inorganic/organic balance of the fungicide is 1.0 or less, and the melting point or decomposition point and molecular weight are as follows:
The manufacturing method according to claim 1, characterized in that (1), (2), (3) and (4) are simultaneously satisfied. 7m+9M≧3150 (1) 5m+6M≦3600 (2) m≧5 (3) M≧100 (4) In the formula, m represents the melting point or decomposition point (°C), and M represents the molecular weight.
JP9219981A 1981-06-17 1981-06-17 Production of polyurethane fiber having anti-fungal property Granted JPS57210068A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9219981A JPS57210068A (en) 1981-06-17 1981-06-17 Production of polyurethane fiber having anti-fungal property

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9219981A JPS57210068A (en) 1981-06-17 1981-06-17 Production of polyurethane fiber having anti-fungal property

Publications (2)

Publication Number Publication Date
JPS57210068A JPS57210068A (en) 1982-12-23
JPS642707B2 true JPS642707B2 (en) 1989-01-18

Family

ID=14047771

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9219981A Granted JPS57210068A (en) 1981-06-17 1981-06-17 Production of polyurethane fiber having anti-fungal property

Country Status (1)

Country Link
JP (1) JPS57210068A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58155462A (en) * 1982-03-10 1983-09-16 Nec Corp State monitoring device
GB8822206D0 (en) * 1988-09-21 1988-10-26 Unilever Plc Fabric treatment composition

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2548193B1 (en) * 1983-06-29 1985-10-18 Commissariat Energie Atomique PRODUCT CONSTITUTING BY A POLYMER OR A COPOLYMER COMPRISING IN ITS CHAIN GROUPS HAVING A THINOMBINE AFFINITY, ITS PREPARATION METHOD AND ITS USE FOR THE SEPARATION AND PURIFICATION OF THROMBIN

Also Published As

Publication number Publication date
JPS57210068A (en) 1982-12-23

Similar Documents

Publication Publication Date Title
US5254134A (en) Textile-finishing agent
EP1269848A1 (en) Antibacterial agent for fiber and antibacterial textile product
US3817702A (en) Antimicrobial textile materials
JPS642707B2 (en)
JPH083873A (en) Antibacterial textile product and production thereof
DE60027951T2 (en) Cellulose fibers containing fabric
JPS61239082A (en) Synthetic fiber excellent in antibacterial and antifungal property
JP3165235B2 (en) Antibacterial processed fiber product and its processing method
US3508858A (en) Process and product for improving the textile characteristics of natural and synthetic fibers and fibers obtained thereby
CN118207651B (en) Soft skin-friendly polypropylene fiber and preparation method thereof
CN111395005A (en) Production process of mothproof and bacteriostatic woolen sweater
JP4038034B2 (en) Cationic antibacterial processing combination agent and antibacterial processing method
JPS61245378A (en) Antibacterial polyester fiber
JP3055569B2 (en) How to prevent yellowing of polyamide fibers with vanillin
US564928A (en) Helens rachel hirschler
JP3259834B2 (en) Polyamide fiber products
US3661501A (en) Catalytic treatment of shaped articles made from fiber-forming synthetic polymers
JPH07216738A (en) Synthetic fiber having antibacterial property and method for producing the same
JPH0429780B2 (en)
KR20090110235A (en) Antimicrobial Fabrics and Methods for Making the Same
JPS5921777A (en) Production of anti-bacterial polyester fiber
CN119465627A (en) Antibacterial washable composite fabric and preparation process thereof
JPH0782663A (en) Production of antifungal fibers
JP2583045B2 (en) Method for deodorizing cellulosic fiber products
JPS58156074A (en) Sterilizable fiber molded article