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
Links
- 229920006306 polyurethane fiber Polymers 0.000 claims description 21
- 229920000728 polyester Polymers 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000000835 fiber Substances 0.000 claims description 6
- 238000002844 melting Methods 0.000 claims description 5
- 230000008018 melting Effects 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 238000000354 decomposition reaction Methods 0.000 claims description 4
- 230000000855 fungicidal effect Effects 0.000 claims description 4
- 239000000417 fungicide Substances 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000003429 antifungal agent Substances 0.000 description 3
- 229940121375 antifungal agent Drugs 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- -1 adipic acid Chemical class 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002731 mercury compounds Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 238000012643 polycondensation polymerization Methods 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 125000001453 quaternary ammonium group Chemical class 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
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)
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.
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)
| 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)
| 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 |
-
1981
- 1981-06-17 JP JP9219981A patent/JPS57210068A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS57210068A (en) | 1982-12-23 |
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