JPH01260065A - Treatment of synthetic yarn - Google Patents
Treatment of synthetic yarnInfo
- Publication number
- JPH01260065A JPH01260065A JP63087827A JP8782788A JPH01260065A JP H01260065 A JPH01260065 A JP H01260065A JP 63087827 A JP63087827 A JP 63087827A JP 8782788 A JP8782788 A JP 8782788A JP H01260065 A JPH01260065 A JP H01260065A
- Authority
- JP
- Japan
- Prior art keywords
- synthetic yarn
- treatment
- quaternary ammonium
- polyester
- ammonium salt
- 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
Links
- 238000011282 treatment Methods 0.000 title abstract description 31
- 229920000728 polyester Polymers 0.000 claims abstract description 28
- 210000004243 sweat Anatomy 0.000 claims abstract description 22
- 239000007864 aqueous solution Substances 0.000 claims abstract description 15
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims abstract description 15
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 13
- 229920002994 synthetic fiber Polymers 0.000 claims description 22
- 239000012209 synthetic fiber Substances 0.000 claims description 22
- 238000010521 absorption reaction Methods 0.000 claims description 14
- 230000000844 anti-bacterial effect Effects 0.000 claims description 14
- 230000001877 deodorizing effect Effects 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- -1 terephthalic acid Chemical compound 0.000 abstract description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 8
- 244000005700 microbiome Species 0.000 abstract description 7
- 229920001515 polyalkylene glycol Polymers 0.000 abstract description 7
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 abstract description 6
- 239000006096 absorbing agent Substances 0.000 abstract description 6
- 239000003945 anionic surfactant Substances 0.000 abstract description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract description 2
- 239000006185 dispersion Substances 0.000 abstract description 2
- 230000000845 anti-microbial effect Effects 0.000 abstract 2
- 239000004599 antimicrobial Substances 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000000835 fiber Substances 0.000 description 30
- 239000004744 fabric Substances 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 5
- 208000016253 exhaustion Diseases 0.000 description 5
- 235000014676 Phragmites communis Nutrition 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 239000003242 anti bacterial agent Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000005372 silanol group Chemical group 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920001451 polypropylene glycol Polymers 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 230000035755 proliferation Effects 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 208000017520 skin disease Diseases 0.000 description 2
- WMRCTEPOPAZMMN-UHFFFAOYSA-N 2-undecylpropanedioic acid Chemical compound CCCCCCCCCCCC(C(O)=O)C(O)=O WMRCTEPOPAZMMN-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical class COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229910020175 SiOH Inorganic materials 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 229940006460 bromide ion Drugs 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 1
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000012770 industrial material Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- 229940006461 iodide ion Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000005825 oxyethoxy group Chemical group [H]C([H])(O[*:1])C([H])([H])O[*:2] 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は合成繊維の処理方法に関するものであり、更に
詳しくは、耐久性のある、優れた吸汗性と、特に悪臭・
皮膚障害の原因となる微生物の繁殖を抑制するのに優れ
た性能を付与するにある。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for treating synthetic fibers.
The purpose is to provide excellent performance in suppressing the proliferation of microorganisms that cause skin disorders.
(従来の技術)
合成繊維、特にポリエチレンテレフタレート繊維に代表
されるポリエステル繊維は優れた物性、例えば優れた寸
法安定性、形態安定性、防しわ性、イージーケア性、強
伸度等を有することから、衣料用、産業資材用等として
広く用いられている。(Prior art) Synthetic fibers, especially polyester fibers represented by polyethylene terephthalate fibers, have excellent physical properties such as excellent dimensional stability, morphological stability, wrinkle resistance, easy care properties, strength and elongation, etc. It is widely used for , clothing, industrial materials, etc.
また、さらに、特公昭46−13197により開示され
ているポリエステル繊維製品の性質改善法により、ポリ
エステル繊維に吸湿性、吸汗性、帯電防止性等の機能性
を付与し、肌着、スポーツウェア裏地等の分野にもポリ
エステル繊維製品が使用されるようになっている。しか
しながら、このような吸湿性、吸汗性が付与されたポリ
エステル繊維はその高い水分保持性のために、常に水分
率の高い状態となり、微生物が繁殖するには好適な場と
もなる。In addition, the method for improving the properties of polyester fiber products disclosed in Japanese Patent Publication No. 46-13197 provides functionality such as hygroscopicity, sweat absorption, and antistatic properties to polyester fibers, making them suitable for use in underwear, sportswear linings, etc. Polyester fiber products are also being used in the field. However, polyester fibers endowed with such hygroscopic and sweat-absorbing properties always have a high moisture content due to their high water retention properties, and thus provide a suitable place for microorganisms to propagate.
(発明が解決しようとする課題)
本発明は、吸湿性、吸汗性の低い合成繊維に、吸湿、吸
汗性を付与するにあたり、合成繊維の優れた物性、耐久
性のある吸湿、吸汗性を損なうことなく、また、悪臭・
皮膚障害の原因となる微生物が繁殖することのない合成
繊維の処理方法を提供することを目的とする。(Problems to be Solved by the Invention) In imparting moisture and sweat absorption properties to synthetic fibers with low moisture absorption and sweat absorption properties, the present invention impairs the excellent physical properties and durable moisture absorption and sweat absorption properties of synthetic fibers. Also, there is no bad odor.
The purpose of the present invention is to provide a method for processing synthetic fibers that does not allow the proliferation of microorganisms that cause skin disorders.
(課題を解決するための手段)
本発明は、合成繊維を、ポリオキシアルキレン鎖を有す
る水分散性ポリエステル加工剤で処理する吸汗加工にお
いて、合成繊維が予めオルガノシリコーン第4級アンモ
ニウム塩を主成分とする抗菌防臭加工剤の水溶液で処理
されていることを特徴とする合成繊維の処理方法である
。(Means for Solving the Problems) The present invention provides a sweat absorbing treatment in which synthetic fibers are treated with a water-dispersible polyester finishing agent having a polyoxyalkylene chain. This is a method for treating synthetic fibers, characterized in that the fibers are treated with an aqueous solution of an antibacterial and deodorizing agent.
本発明でいう合成繊維とは吸湿性の低い合成繊維であり
、ポリエステル系繊維、ポリアミド系繊維、アクリル系
繊維等が挙げられる0本発明の効果が最も顕著に発現さ
れる点でポリエステル系繊維が好ましい。The synthetic fibers referred to in the present invention are synthetic fibers with low hygroscopicity, and include polyester fibers, polyamide fibers, acrylic fibers, etc. Polyester fibers are the most effective in achieving the effects of the present invention. preferable.
本発明の方法を適用するポリエステル系繊維は、ポリエ
チレンテレフタレート、ポリブチレンテレフタレート、
ポリシクロヘキサンジメチルテレフタレートなどのアル
キレンテレフタレートまたは共重合ポリエステルから製
造された繊維を意味するものである。Polyester fibers to which the method of the present invention is applied include polyethylene terephthalate, polybutylene terephthalate,
It refers to fibers made from alkylene terephthalates such as polycyclohexane dimethyl terephthalate or copolyesters.
ここでいう共重合ポリエステルとは、上記アルキレンテ
レフタレートを構成する成分に、アゼライン酸、セバシ
ン酸、アジピン酸、ドデカンジカルボン酸などの脂肪族
ジカルボン酸、イソフタル酸、5−ナトリウムスルホイ
ソフタル酸、ナフタレンジカルボン酸、ジフェニルエタ
ン−4,4’ −ジカルボン酸などの芳香族ジカルボン
酸、シクロヘキサンジカルボン酸などの脂環式ジカルボ
ン酸のような他のジカルボン酸成分やプロピレングリコ
ール、1.3−ベンタンジオール、1.6−ヘキサンジ
オール、ネオペンチルグリコール、デカメチレングリコ
ール、シクロヘキサンジメタツール、シクロヘキサンジ
オールなどの脂肪族グリコール、ポリエチレングリコー
ル、ポリテトラメチレングリコールなどの長鎖グリコー
ルなどの他のジオール成分、オキシ安息香酸、オキシエ
トキシ安息香酸などのオキシ酸成分の少なくとも1種を
少割合共重合したポリエステルである。The copolymerized polyester referred to herein means that the components constituting the alkylene terephthalate include aliphatic dicarboxylic acids such as azelaic acid, sebacic acid, adipic acid, and dodecanedicarboxylic acid, isophthalic acid, 5-sodium sulfoisophthalic acid, and naphthalene dicarboxylic acid. , aromatic dicarboxylic acids such as diphenylethane-4,4'-dicarboxylic acid, cycloaliphatic dicarboxylic acids such as cyclohexanedicarboxylic acid, propylene glycol, 1,3-bentanediol, 1.6 - Other diol components such as aliphatic glycols such as hexanediol, neopentyl glycol, decamethylene glycol, cyclohexane dimetatool, cyclohexanediol, long chain glycols such as polyethylene glycol, polytetramethylene glycol, oxybenzoic acid, oxyethoxy It is a polyester obtained by copolymerizing a small proportion of at least one oxyacid component such as benzoic acid.
本発明では、合成繊維を、ポリオキシアルキレン鎖を有
する水分散性ポリエステル加工剤により吸汗加工する。In the present invention, synthetic fibers are subjected to sweat absorption processing using a water-dispersible polyester processing agent having a polyoxyalkylene chain.
ここでいう水分散性ポリエステル加工剤とは、テレフタ
ル酸やイソフタル酸などのジカルボン酸とアルキレング
リコールおよびポリアルキレングリコール、ポリアルキ
レングリコールモノエーテル等のブロック共重合体の水
分散液であり、上記ブロック共重合体のテレフタレート
単位とイソフタレート単位のモル比は、100:O〜5
0 : 50で、テレフタレート単位およびイソフタレ
ート単位とポリアルキレングリコール単位のモル比は2
〜15:1で、ポリアルキレングリコールの分子量は6
00〜60000である。The water-dispersible polyester processing agent referred to here is an aqueous dispersion of a dicarboxylic acid such as terephthalic acid or isophthalic acid and a block copolymer such as alkylene glycol, polyalkylene glycol, or polyalkylene glycol monoether. The molar ratio of terephthalate units and isophthalate units in the polymer is 100:O to 5.
0:50, and the molar ratio of terephthalate units and isophthalate units to polyalkylene glycol units is 2
~15:1, and the molecular weight of the polyalkylene glycol is 6
00-60000.
上記アルキレングリコールには、エチレングリコール、
プロピレングリコールテトラメチレングリコール、デカ
メチレングリコール等が含まれ、ポリアルキレングリコ
ールには、ポリエチレングリコール、ポリプロピレング
リコール等が含まれる。また、ポリアルキレングリコー
ルモノエーテルには、ポリエチレングリコール、ポリプ
ロピレングリコール、ポリプロピレングリコール等のモ
ノメチルエーテル、モノエチルエーテル等が含まれる。The above alkylene glycol includes ethylene glycol,
Propylene glycol includes tetramethylene glycol, decamethylene glycol, etc., and polyalkylene glycol includes polyethylene glycol, polypropylene glycol, etc. Further, polyalkylene glycol monoethers include monomethyl ethers, monoethyl ethers, etc. of polyethylene glycol, polypropylene glycol, polypropylene glycol, and the like.
これらブロック共重合体は、通常、被処理繊維に対し、
0,1〜5,0%(重量)、好ましくは0.5〜3.0
%(重量)使用する。These block copolymers usually have a
0.1-5.0% (by weight), preferably 0.5-3.0
% (weight) used.
本発明に於ては、合成繊維を上記吸汗加工する前に、予
め該合成繊維がオルガノシリコーン第4級アンモニウム
塩を主成分とする抗菌防臭加工剤の水溶液で処理されて
いることが必要である。この処理の順序が逆の場合、あ
るいは同浴同時処理では吸汗性において優れた効果を得
ることができない。In the present invention, before the synthetic fiber is subjected to the above-mentioned sweat absorbing treatment, it is necessary that the synthetic fiber is previously treated with an aqueous solution of an antibacterial and deodorizing agent containing an organosilicone quaternary ammonium salt as a main component. . If the order of this treatment is reversed, or if the treatments are performed simultaneously in the same bath, excellent sweat absorption effects cannot be obtained.
この処理によりオルガノシリコーン第4級アンモニウム
塩は繊維に付与されるが、繊維上でのオルガノシリコー
ン化合物はモノマー、ポリマー何れでもよいが好ましく
はポリマーである。その付与量は、該ポリエステル繊維
重量に対して2×10−’mol/g以上で有り、好ま
しくは4 X 10−’mol/g以上である。第4級
アンモニウム塩基を有するオルガノシリコーン化合物の
量が2 X 10−’mol/gに満たない場合、繊維
上での微生物の繁殖抑制の効果が低い、また、ここで使
用する第4級アンモニウム塩基を有するオルガノシリコ
ーン化合物は−形式
リコーン化合物である。上記式中Xは酸アニオン、例え
ば塩素イオン、臭素イオン、沃素イオン、蟻酸アニオン
、酢酸アニオン等であり、Ri;tc+〜C2゜のアル
キル基、R′は炭素原子20以下の2価の炭化水素基又
はアルキル基又は酸素を−C0C−1た、窒素をR″N
−基(R″はH又は低級アルキル)の形で含有する基、
Yは一1SiY+tlOH→=SiOH+ IIYの如
く水と反応してシラノール基を形成する珪素結合基で、
メトオキシ基、エトオキシ基やハロゲン原子が含まれる
。Yはもちろん一〇H基であってもよい0mはO又は1
の値である。好ましい化合物の例を上げると
(CH30Ss 5iCHz CHz CHz N −
(CH3)z C+5Hs7C+の化合物がある。メト
キシ基、エトキシ基のように加水分解可能基は水性処理
媒体に添加された場合、水と反応してシラノール基を作
成し、繊維表面の活性水素と反応し、次いで、シラノー
ル基は縮合して繊維表面をシロキサンで被覆する。この
ように、オルガノシリコーン化合物は繊維上に固着され
ているために、汗等により繊維表面から移動することな
く、恒久的に抗菌効果を維持することができる。The organosilicone quaternary ammonium salt is applied to the fibers by this treatment, and the organosilicone compound on the fibers may be either a monomer or a polymer, but preferably a polymer. The amount applied is at least 2 x 10-' mol/g, preferably at least 4 x 10-' mol/g, based on the weight of the polyester fiber. If the amount of the organosilicone compound having a quaternary ammonium base is less than 2 × 10-' mol/g, the effect of inhibiting the growth of microorganisms on the fiber is low; The organosilicone compound having the formula is a -form silicone compound. In the above formula, X is an acid anion, such as a chloride ion, bromide ion, iodide ion, formate anion, acetate anion, etc., Ri is an alkyl group of tc+ to C2°, and R' is a divalent hydrocarbon having 20 or less carbon atoms. group or alkyl group or oxygen is -C0C-1, nitrogen is R″N
- a group containing in the form of a group (R'' is H or lower alkyl),
Y is a silicon-bonded group that reacts with water to form a silanol group, such as -1SiY+tlOH→=SiOH+IIY,
Contains methoxy groups, ethoxy groups and halogen atoms. Of course, Y may be a 10H group. 0m is O or 1
is the value of Examples of preferred compounds are (CH30Ss 5iCHz CHz CHz N -
There is a compound of (CH3)z C+5Hs7C+. When hydrolyzable groups such as methoxy and ethoxy groups are added to an aqueous treatment medium, they react with water to create silanol groups, which react with active hydrogen on the fiber surface, and then the silanol groups condense and form silanol groups. The fiber surface is coated with siloxane. In this way, since the organosilicone compound is fixed on the fiber, it can permanently maintain its antibacterial effect without being moved from the fiber surface due to sweat or the like.
オルガノシリコーン第4級アンモニウム塩処理は、合成
繊維が、糸状、ウェブ状、あるいは織編物状のどの形態
においても実施できる0例えば合成繊維の製造段階で、
ローラーやガイドにより、オルガノシリコーン第4級ア
ンモニウム塩の水希釈液をオイリングと同じ要領で付与
し、または、繊維塊にスプレー、または、ディッピング
法で該水希釈液を付与し、加熱・乾燥しても良いし、ま
た、合成繊維の短繊維、長繊維の糸を織物あるいは編物
とした後、液中吸尽処理、パッド乾燥処理しても良い、
上記液中吸尽処理の処理条件は、通常浴比1:5〜10
0で、常温〜80°C1好ましくは40〜70°Cで3
0分以上吸尽処理し、80°C以上の熱風乾燥により仕
上げられる。Organosilicone quaternary ammonium salt treatment can be carried out on synthetic fibers in any form, such as filaments, webs, or woven or knitted fabrics. For example, at the manufacturing stage of synthetic fibers,
A water diluted solution of organosilicone quaternary ammonium salt is applied using a roller or guide in the same manner as oiling, or the water diluted solution is applied to the fiber mass by spraying or dipping, followed by heating and drying. Alternatively, short synthetic fibers or long fibers may be woven or knitted, and then subjected to submerged exhaustion treatment and pad drying treatment.
The treatment conditions for the above-mentioned submerged exhaustion treatment are usually a bath ratio of 1:5 to 10.
0, normal temperature to 80°C 1 preferably 40 to 70°C 3
Finished by exhaustion treatment for 0 minutes or more and hot air drying at 80°C or more.
本発明においては、上記オルガノシリコーン第4級アン
モニウム塩を主成分とする抗菌防臭加工剤の水溶液が、
下記−形式のようなアニオン系界面活性剤を含むことが
好ましい。In the present invention, an aqueous solution of an antibacterial and deodorizing agent containing the organosilicone quaternary ammonium salt as a main component,
Preferably, an anionic surfactant of the type below is included.
一般式 (ただし式中Rはアルキル基を、Mは水素原子。general formula (However, in the formula, R is an alkyl group, and M is a hydrogen atom.
−NH4,またはアルカリ金属を示す。nは1〜100
゜)上記アニオン系界面活性剤を含むオルガノシリコー
ン第4級アンモニウム塩の水溶液で処理した合成繊維は
濡れ性が良好で、前述の次工程の吸汗加工において、処
理側の浸透性が向上すると共に、吸汗性の向上にもつな
がる。処理液におけるアニオン系界面活性剤の配合量は
、アニオン系界面活性剤:オルガノシリコーン第4級ア
ンモニウム塩のモル比が0.2〜2:1、好ましくは、
0.5〜l:■となる量であり、アニオン系界面活性剤
のオルガノシリコーン第4級アンモニウム塩に対する割
合が小さすぎると初期の効果が発現されず、逆に、当該
割合が大きすぎると、吸汗加工剤の固着性が低下する。-NH4, or an alkali metal. n is 1 to 100
゜) Synthetic fibers treated with the aqueous solution of organosilicone quaternary ammonium salt containing the anionic surfactant have good wettability, and in the sweat absorption process of the next step described above, the permeability on the treated side is improved, It also leads to improved sweat absorption. The amount of anionic surfactant blended in the treatment liquid is such that the molar ratio of anionic surfactant:organosilicone quaternary ammonium salt is 0.2 to 2:1, preferably,
The amount is 0.5 to 1:■, and if the ratio of the anionic surfactant to the organosilicone quaternary ammonium salt is too small, the initial effect will not be expressed, and on the contrary, if the ratio is too large, The adhesion of the sweat absorbing agent decreases.
本発明では、合成繊維を上記オルガノシリコーン第4級
アンモニウム塩を主成分とする抗菌防臭加工剤の水溶液
で処理した後、前述の吸汗加工剤により処理するが、処
理方法としては、液中吸尽処理、パッド乾燥処理が適用
される。液中吸尽処理においては、オルガノシリコーン
第4級アンモニウム塩水溶液処理が、液中吸尽処理で実
施されている場合は、該オルガノシリコーン第4級アン
モニウム塩水溶液処理の終了後、引き続き、同浴に吸汗
加工剤を投入しての処理も可能である。In the present invention, synthetic fibers are treated with an aqueous solution of an antibacterial and deodorizing agent containing the organosilicone quaternary ammonium salt as a main component, and then treated with the sweat-absorbing agent described above. treatment, pad drying treatment is applied. In the in-liquid exhaustion treatment, if the organosilicone quaternary ammonium salt aqueous solution treatment is carried out by the in-liquid exhaustion treatment, after the completion of the organosilicone quaternary ammonium salt aqueous solution treatment, the organosilicone quaternary ammonium salt aqueous solution treatment is It is also possible to add a sweat-absorbing agent to the material.
(実施例) 以下本発明の実施例について説明する。(Example) Examples of the present invention will be described below.
実施例1
ポリエステルマルチフィラメント系(63デニール/1
08フイラメント)を用い、シングルトリコット411
(カールマイヤー社製KE−2型28ゲージ130イン
チ幅)のフロント筬および、バック筬に通し、フロント
筬組織!−37,−,と、バック筬&lt@’−’/、
−。Example 1 Polyester multifilament type (63 denier/1
08 filament), single tricot 411
(KE-2 type 28 gauge 130 inch width manufactured by Karl Mayer) through the front reed and back reed, and the front reed structure! -37,-, and back reed <@'-'/,
−.
とからなるトリコット編地を編成した。得られた生機編
地を起毛、精練染色後、式
オン系界面活性剤0.16%0″を含む抗菌剤3−トリ
メトキシリル−プロピル−ジメチル−アンモニウムクロ
ライド(商品名DC−5700・ダウコーニング社製)
0.25%”’ (7)水溶液で浴比1:50,60
″Cで30分間吸尽処理し、脱水・乾燥した。その後、
水分散性ポリエステル系吸汗加工剤(商品名5R−to
oo・高松油脂社製) 40g/ Qの処理液を用いて
ウェット・ピック・アップ70%でパッド乾燥法により
加工、仕上げセットし、抗菌防臭性、吸汗性ポリエステ
ル繊維編地を得た。A tricot knitted fabric consisting of The obtained greige knitted fabric was raised, scoured and dyed, and then treated with an antibacterial agent 3-trimethoxylyl-propyl-dimethyl-ammonium chloride (trade name: DC-5700, Dow Corning) containing 0.16% 0'' of formula-on surfactant. company)
0.25%"' (7) Aqueous solution with bath ratio 1:50,60
"C" for 30 minutes, dehydrated and dried. Then,
Water-dispersible polyester sweat absorbing agent (product name 5R-to)
Using a treatment solution of 40 g/Q (manufactured by Takamatsu Yushi Co., Ltd.), it was processed and finished by a pad drying method with a wet pick-up of 70%, and an antibacterial, deodorizing and sweat-absorbing polyester fiber knitted fabric was obtained.
実施例2
上記実施例1において、抗菌剤水溶液処理をパッド・乾
燥法で行なった以外は全く同様にして抗菌防臭性、吸汗
性ポリエステル繊維編地を得た。Example 2 An antibacterial, deodorizing and sweat-absorbing polyester fiber knitted fabric was obtained in exactly the same manner as in Example 1, except that the antibacterial agent aqueous solution treatment was carried out by the pad drying method.
比較例1
上記実施例1において、吸汗加工剤処理を施さない以外
は全く同様にして抗菌防臭性ポリエステル繊維編地を得
た。Comparative Example 1 An antibacterial and deodorizing polyester fiber knitted fabric was obtained in exactly the same manner as in Example 1, except that the sweat absorbent treatment was not performed.
比較例2
上記実施例1において、抗菌剤水溶液処理を施さない以
外は全く同様にして、吸汗性ポリエステル繊維編地を得
た。Comparative Example 2 A sweat-absorbing polyester fiber knitted fabric was obtained in exactly the same manner as in Example 1, except that the antibacterial aqueous solution treatment was not performed.
比較例3
上記実施例1において、抗菌剤水溶液処理、吸汗加工剤
処理を施さない以外は全く同様にしてポリエステル繊維
編地を得た。Comparative Example 3 A polyester fiber knitted fabric was obtained in exactly the same manner as in Example 1 above, except that the antibacterial agent aqueous solution treatment and the sweat absorbing agent treatment were not performed.
比較例4
上記実施例1において、抗菌剤水溶液による処理と吸汗
加工剤による処理の順序を変えた以外はまったく同様に
して加工し、仕上げセットし、抗菌防臭性・吸汗性ポリ
エステル繊維編地を得た。Comparative Example 4 A fabric was processed in exactly the same manner as in Example 1 above, except that the order of the treatment with the antibacterial agent aqueous solution and the treatment with the sweat-absorbing finishing agent was changed, and finishing and setting were carried out to obtain an antibacterial, deodorizing and sweat-absorbing polyester fiber knitted fabric. Ta.
比較例5
実施例1のトリコント編地を、式
キシシリル−プロピル−ジメチル−アンモニウムクロラ
イド3.6g/ffiおよび水分散性ポリエステル系吸
汗加工剤(SR−1000) 40g/ j1!の同浴
処理液で加工しくウェット・ピック・アップ70%)仕
上げセットして抗菌防臭性・吸汗性ポリエステル繊維編
地を得た。Comparative Example 5 The triconte knitted fabric of Example 1 was treated with 3.6 g/ffi of the formula xysilyl-propyl-dimethyl-ammonium chloride and 40 g/j1! of a water-dispersible polyester sweat-absorbing finishing agent (SR-1000). The fabric was treated with the same bath treatment solution and finished with a wet pick-up (70%) to obtain an antibacterial, deodorizing, and sweat-absorbing polyester fiber knitted fabric.
上記の実施例及び、比較例で得られたポリエステル繊維
編地を試料として、抗菌性及び吸汗性を調べた。The polyester fiber knitted fabrics obtained in the above Examples and Comparative Examples were used as samples to examine antibacterial properties and sweat absorption properties.
その結果を第1表に示す。The results are shown in Table 1.
試験法
抗菌性:シェイクフラスコ法(米国AATCCTest
Method 100に準じる。供試菌タレブシーラニ
ューモエア)
吸汗性:(1) ウィッキングテスト(水浸透性)(
2) バイシック法
第 1 表
(発明の効果)
第1表かられかるように、本発明の合成繊維の処理方法
による合成繊維を用いた製品は、優れた吸汗性を有する
と共に、微生物の増殖を有効に抑制して不快臭の発生を
防止し、肌着、スポーツウェア裏地として最適である。Test method Antibacterial property: Shake flask method (USA AATCCTest
According to Method 100. Test bacterium Talebsiella pneumoea) Sweat absorption: (1) Wicking test (water permeability) (
2) Bisic Method Table 1 (Effects of the Invention) As shown in Table 1, products using synthetic fibers produced by the synthetic fiber processing method of the present invention have excellent sweat absorption properties and are highly resistant to the growth of microorganisms. It effectively suppresses unpleasant odors and is ideal as a lining for underwear and sportswear.
特許出願人 東洋紡績株式会社Patent applicant: Toyobo Co., Ltd.
Claims (1)
いて、合成繊維が予め、オルガノシリコーン第4級アン
モニウム塩を主成分とする抗菌防臭加工剤の水溶液で処
理されていることを特徴とする合成繊維の処理方法。[Scope of Claims] In sweat absorption processing in which synthetic fibers are treated with a water-dispersible polyester finishing agent having a polyoxyalkylene chain, the synthetic fibers are treated with an antibacterial and deodorizing finishing agent whose main component is an organosilicone quaternary ammonium salt. A method for treating synthetic fibers, characterized by being treated with an aqueous solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63087827A JPH01260065A (en) | 1988-04-08 | 1988-04-08 | Treatment of synthetic yarn |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63087827A JPH01260065A (en) | 1988-04-08 | 1988-04-08 | Treatment of synthetic yarn |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01260065A true JPH01260065A (en) | 1989-10-17 |
Family
ID=13925784
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63087827A Pending JPH01260065A (en) | 1988-04-08 | 1988-04-08 | Treatment of synthetic yarn |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01260065A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5411585A (en) * | 1991-02-15 | 1995-05-02 | S. C. Johnson & Son, Inc. | Production of stable hydrolyzable organosilane solutions |
WO1997006675A1 (en) * | 1995-08-18 | 1997-02-27 | Rhodia Limited | Biocidal compositions |
JP2001294810A (en) * | 2000-04-12 | 2001-10-23 | Shin Etsu Chem Co Ltd | Underwater antifouling paint composition |
WO2019176654A1 (en) * | 2018-03-12 | 2019-09-19 | 東レ株式会社 | Polyester fiber structure |
-
1988
- 1988-04-08 JP JP63087827A patent/JPH01260065A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5411585A (en) * | 1991-02-15 | 1995-05-02 | S. C. Johnson & Son, Inc. | Production of stable hydrolyzable organosilane solutions |
WO1997006675A1 (en) * | 1995-08-18 | 1997-02-27 | Rhodia Limited | Biocidal compositions |
JP2001294810A (en) * | 2000-04-12 | 2001-10-23 | Shin Etsu Chem Co Ltd | Underwater antifouling paint composition |
WO2019176654A1 (en) * | 2018-03-12 | 2019-09-19 | 東レ株式会社 | Polyester fiber structure |
JPWO2019176654A1 (en) * | 2018-03-12 | 2021-01-14 | 東レ株式会社 | Polyester fiber structure |
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