JPH0411076A - Production of antimicrobial and deodorizing fabric - Google Patents
Production of antimicrobial and deodorizing fabricInfo
- Publication number
- JPH0411076A JPH0411076A JP2114467A JP11446790A JPH0411076A JP H0411076 A JPH0411076 A JP H0411076A JP 2114467 A JP2114467 A JP 2114467A JP 11446790 A JP11446790 A JP 11446790A JP H0411076 A JPH0411076 A JP H0411076A
- Authority
- JP
- Japan
- Prior art keywords
- fabric
- melamine derivative
- derivative compound
- antibacterial
- antimicrobial
- 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
- 239000004744 fabric Substances 0.000 title claims abstract description 48
- 230000001877 deodorizing effect Effects 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 230000000845 anti-microbial effect Effects 0.000 title abstract 3
- -1 melamine derivative compound Chemical class 0.000 claims abstract description 27
- 239000000835 fiber Substances 0.000 claims abstract description 13
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims abstract description 11
- 239000003054 catalyst Substances 0.000 claims abstract description 9
- 230000000844 anti-bacterial effect Effects 0.000 claims description 26
- 239000003242 anti bacterial agent Substances 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 4
- 239000011259 mixed solution Substances 0.000 claims description 3
- 238000000151 deposition Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 25
- 238000011282 treatment Methods 0.000 abstract description 12
- 238000005406 washing Methods 0.000 abstract description 12
- 229920002994 synthetic fiber Polymers 0.000 abstract description 7
- 239000012209 synthetic fiber Substances 0.000 abstract description 7
- YGCOKJWKWLYHTG-UHFFFAOYSA-N [[4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]-(hydroxymethyl)amino]methanol Chemical compound OCN(CO)C1=NC(N(CO)CO)=NC(N(CO)CO)=N1 YGCOKJWKWLYHTG-UHFFFAOYSA-N 0.000 abstract description 3
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 abstract description 2
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 abstract description 2
- 229960001763 zinc sulfate Drugs 0.000 abstract description 2
- 229910000368 zinc sulfate Inorganic materials 0.000 abstract description 2
- 239000004599 antimicrobial Substances 0.000 abstract 4
- 239000002781 deodorant agent Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000007598 dipping method Methods 0.000 abstract 1
- 150000007974 melamines Chemical class 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 24
- 239000011347 resin Substances 0.000 description 24
- 238000009472 formulation Methods 0.000 description 22
- 238000000034 method Methods 0.000 description 19
- 230000000052 comparative effect Effects 0.000 description 15
- 241000894006 Bacteria Species 0.000 description 8
- 229920000742 Cotton Polymers 0.000 description 8
- 238000004043 dyeing Methods 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- ACINEQKBTSRMIM-UHFFFAOYSA-N benzyl-methyl-octadecylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[NH+](C)CC1=CC=CC=C1 ACINEQKBTSRMIM-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- USDJGQLNFPZEON-UHFFFAOYSA-N [[4,6-bis(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(NCO)=NC(NCO)=N1 USDJGQLNFPZEON-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- OJIYIVCMRYCWSE-UHFFFAOYSA-M Domiphen bromide Chemical compound [Br-].CCCCCCCCCCCC[N+](C)(C)CCOC1=CC=CC=C1 OJIYIVCMRYCWSE-UHFFFAOYSA-M 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229920000577 Nylon 6/66 Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- SYDYRFPJJJPJFE-UHFFFAOYSA-N [[4,6-bis[bis(hydroxymethyl)amino]-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(N(CO)CO)=NC(N(CO)CO)=N1 SYDYRFPJJJPJFE-UHFFFAOYSA-N 0.000 description 1
- SUPOBRXPULIDDX-UHFFFAOYSA-N [[4-amino-6-(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound NC1=NC(NCO)=NC(NCO)=N1 SUPOBRXPULIDDX-UHFFFAOYSA-N 0.000 description 1
- BJSBGAIKEORPFG-UHFFFAOYSA-N [[6-amino-1,2,3,4-tetramethoxy-4-(methoxyamino)-1,3,5-triazin-2-yl]-methoxyamino]methanol Chemical compound CONC1(N(C(N(C(=N1)N)OC)(N(CO)OC)OC)OC)OC BJSBGAIKEORPFG-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- NGPGDYLVALNKEG-UHFFFAOYSA-N azanium;azane;2,3,4-trihydroxy-4-oxobutanoate Chemical compound [NH4+].[NH4+].[O-]C(=O)C(O)C(O)C([O-])=O NGPGDYLVALNKEG-UHFFFAOYSA-N 0.000 description 1
- TZYHIGCKINZLPD-UHFFFAOYSA-N azepan-2-one;hexane-1,6-diamine;hexanedioic acid Chemical compound NCCCCCCN.O=C1CCCCCN1.OC(=O)CCCCC(O)=O TZYHIGCKINZLPD-UHFFFAOYSA-N 0.000 description 1
- UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
- 229960001950 benzethonium chloride Drugs 0.000 description 1
- XKXHCNPAFAXVRZ-UHFFFAOYSA-N benzylazanium;chloride Chemical compound [Cl-].[NH3+]CC1=CC=CC=C1 XKXHCNPAFAXVRZ-UHFFFAOYSA-N 0.000 description 1
- SXPWTBGAZSPLHA-UHFFFAOYSA-M cetalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SXPWTBGAZSPLHA-UHFFFAOYSA-M 0.000 description 1
- 229960000228 cetalkonium chloride Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- JCALZGYNNQTXGP-UHFFFAOYSA-M dimethyl-[[4-(6-methylheptyl)phenyl]methyl]-[2-(2-phenoxyethoxy)ethyl]azanium chloride Chemical compound [Cl-].C(CCCCC(C)C)C1=CC=C(C[N+](C)(C)CCOCCOC2=CC=CC=C2)C=C1 JCALZGYNNQTXGP-UHFFFAOYSA-M 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910001960 metal nitrate Inorganic materials 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000000985 reactive dye Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、染色堅牢度に優れ、良好な風合を有し、洗濯
耐久性にも優れた抗菌防臭布帛の製造方法に関するもの
である。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for producing an antibacterial and deodorizing fabric that has excellent color fastness, good hand feel, and excellent washing durability.
(従来の技術)
我々は2日常生活の中で細菌やカビ等の微生物の悪影響
を受けている。特に衣料品、寝装品、インテリア品等の
繊維製品においては、繊維表面に付着した汗、垢、汚れ
等を栄養源にして繁殖した細菌やカビ等の微生物によっ
て、悪臭を発したり。(Prior Art) In our daily lives, we are adversely affected by microorganisms such as bacteria and mold. In particular, textile products such as clothing, bedding, and interior goods can emit bad odors due to microorganisms such as bacteria and mold that propagate using sweat, grime, dirt, etc. adhering to the fiber surface as a nutrient source.
繊維を脆化したりして、実用上あるいは衛生上で悪影響
を受けている。こうした状況の中で快適な衣生活や健康
的な生活環境を形成するうえで、繊維製品の抗菌防臭加
工の重要性が認識されるようになってきた。This causes the fibers to become brittle, which has a negative impact on practical and hygienic aspects. Under these circumstances, the importance of antibacterial and deodorizing treatments for textile products has been recognized in creating comfortable clothing and a healthy living environment.
繊維製品の抗菌防臭加工に際しては、(1)衛生効果が
大きいこと、(2)洗濯耐久性があること、(3)人体
に対して安全であること、の3要件を満たさなければな
らない。When applying antibacterial and deodorizing treatment to textile products, three requirements must be met: (1) the product must have a large hygienic effect, (2) it must be durable against washing, and (3) it must be safe for the human body.
これに対して従来より行われている抗菌防臭加工方法は
、衛生効果が大きく、かつ2人体に対して安全な抗菌剤
を用いて、洗濯耐久性向上のだtの種々の方法が試みら
れている。その方法としては、繊維に対して親和力のあ
る抗菌剤を繊維に付着する方法が実用に供されている。On the other hand, conventional antibacterial and deodorizing processing methods have been tried to improve washing durability by using antibacterial agents that have great hygienic effects and are safe for the human body. There is. As a method for this purpose, a method in which an antibacterial agent having an affinity for fibers is attached to the fibers has been put into practical use.
しかし、この方法は、綿製品に効果があるのみで9合成
繊維に対しては洗濯耐久性の効果が十分でなく、それば
かりか、綿製品2合成繊維の双方に対して染色堅牢度を
低下させる問題もあった。However, this method is only effective for cotton products, but does not have a sufficient effect on washing durability for synthetic fibers, and also reduces the color fastness of both synthetic fibers for cotton products. There was also the problem of
(発明が解決しようとする課題)
本発明は、このような現状に鑑みて行われたもので、染
色堅牢度に優れ、良好な風合を有し、洗濯耐久性にも優
れた抗菌防臭性を有する繊維布帛を得ることを目的とす
るものである。(Problems to be Solved by the Invention) The present invention has been made in view of the current situation, and aims to provide an antibacterial and deodorizing property that has excellent color fastness, good texture, and excellent washing durability. The object of the present invention is to obtain a fiber fabric having the following characteristics.
(課題を解決するための手段)
本発明は、上記目的を達成するもので9次の構成を有す
るものである。(Means for Solving the Problems) The present invention achieves the above object and has the following nine configurations.
すなわち9本発明は、布帛に第4級アンモニウム塩系抗
菌剤、メラミン誘導体化合物、メラミン誘導体化合物用
触媒の3種類の混合溶液を含浸し。That is, in the present invention, a fabric is impregnated with a mixed solution of three types: a quaternary ammonium salt antibacterial agent, a melamine derivative compound, and a catalyst for the melamine derivative compound.
該布帛の繊維重量に対して第4級アンモニウム塩系抗菌
剤を0.5〜5.0%、メラミン誘導体化合物を0.1
〜1.0%付着せし島、シかる後に乾燥、熱処理するこ
とを特徴とする染色堅牢度に優れた抗菌防臭布帛の製造
方法を要旨とするものである。0.5 to 5.0% of quaternary ammonium salt antibacterial agent and 0.1% of melamine derivative compound based on the fiber weight of the fabric.
The gist of the present invention is a method for producing an antibacterial and deodorizing fabric with excellent color fastness, which is characterized by drying and heat-treating after drying and heat-treating the fabric to an extent of about 1.0%.
以下9本発明について詳細に説明する。Below, nine aspects of the present invention will be explained in detail.
本発明で用いられる布帛としては、ナイロン6やナイロ
ン66で代表されるポリアミド系合成繊維、ポリエチレ
ンテレフタレートで代表されるポリエステル系合成繊維
、ポリアクリロニトリル系合成繊維、トリアセテート等
の半合成繊維あるいはナイロン6/木綿、ポリエチレン
テレフタレート/木綿等の混紡繊維等から構成された織
物1編物、不織布等を挙げることができる。Fabrics used in the present invention include polyamide synthetic fibers such as nylon 6 and nylon 66, polyester synthetic fibers such as polyethylene terephthalate, polyacrylonitrile synthetic fibers, semi-synthetic fibers such as triacetate, and nylon 6/66. Examples include knitted woven fabrics, nonwoven fabrics, etc. made of cotton, blended fibers such as polyethylene terephthalate/cotton, and the like.
本発明で用いられる第4級アンモニウム塩系抗菌剤は、
従来から一般に使用されている公知の薬剤でよく1例え
ば、3−()IJメトキシシリル)プロピルジメチルオ
クタデシル−アンモニウムクロライド、オクタデシルメ
チル−ベンジルアンモニウムクロライド、塩化ベンゼト
ニウム、ポリオキシエチレントリメチルアンモニウムク
ロライド。The quaternary ammonium salt antibacterial agent used in the present invention is
Examples of commonly used agents include 3-()IJmethoxysilyl)propyldimethyloctadecyl-ammonium chloride, octadecylmethyl-benzylammonium chloride, benzethonium chloride, and polyoxyethylenetrimethylammonium chloride.
p−イソオクチルフェノキシエトキシエチルジメチルベ
ンジルアンモニウムクロライド、ドデシルジメチル(2
−フェノキシエチル)アンモニウムプロミド、セチルジ
メチルベンジルアンモニウムクロライド等を挙げること
ができる。p-isooctylphenoxyethoxyethyldimethylbenzylammonium chloride, dodecyldimethyl (2
-phenoxyethyl) ammonium bromide, cetyldimethylbenzylammonium chloride, and the like.
使用量は、布帛繊維重量に対して0.5〜5.0%の範
囲の付着量になるように処理液濃度を作成し。The concentration of the treatment liquid is determined so that the amount to be used is in the range of 0.5 to 5.0% based on the weight of the fabric fibers.
使用する。ここで0.5%未満であると抗菌性の耐久性
に問題があり、また、5%を超える場合は。use. If it is less than 0.5%, there is a problem with antibacterial durability, and if it exceeds 5%.
抗菌性能において飽和値に達しているた袷、コスト的に
不利となる。If the antibacterial performance has reached the saturation value, it will be disadvantageous in terms of cost.
本発明で用いられるメラミン誘導体化合物は。The melamine derivative compound used in the present invention is.
ヘキサメチロールメラミン、トリメチロールメラミン、
ペンタメチロールメラミン、ヘキサキスメトキシメチロ
ールメラミン、トリスメトキシメチロールメラミン、ト
リスメトキシメチルメラミン。hexamethylolmelamine, trimethylolmelamine,
Pentamethylolmelamine, hexakismethoxymethylolmelamine, trismethoxymethylolmelamine, trismethoxymethylmelamine.
ジメチロールメラミン、ビスメトキシメチルメチロール
メラミン等が挙げられ、これらの中でヘキサメチロール
メラミン、トリメチロールメラミンが特に好ましい。Examples include dimethylolmelamine, bismethoxymethylmethylolmelamine, and among these, hexamethylolmelamine and trimethylolmelamine are particularly preferred.
使用量は、布帛繊維重量に対して0.1〜1.0%の範
囲の付着量になるように処理液濃度を作成し。The concentration of the treatment liquid is determined so that the amount to be used is in the range of 0.1 to 1.0% based on the weight of the fabric fibers.
使用する。ここで0.1%未満であると、染色堅牢度低
下に対する防止効果が発揮されなくなるとともに、抗菌
性の洗濯耐久性向上にも寄与しなくなり、また、1.0
%を超えると、風合が硬くなるため、実用面で繁用性に
かける。use. Here, if it is less than 0.1%, the effect of preventing the decline in color fastness will not be exhibited, and it will not contribute to improving the washing durability of antibacterial properties.
If it exceeds %, the texture will become hard and it will be difficult to use in practical terms.
ここで併用されるメラミン誘導体化合物用触媒は、硫酸
亜鉛、硝酸アルミニウム、塩化アルミニウム、硼弗化亜
鉛のような多価金属の硝酸塩、ハロゲン化物、硼弗化物
等や酒石酸、クエン酸、酒石酸アンモニウム、クエン酸
アンモニウム、塩化アンモニウム等の無機または有機の
酸およびそれらのアンモニウム塩、リン酸/塩化アンモ
ニウムのような塩と遊離酸との混合触媒等であり、これ
らはいずれもメラミン誘導体化合物の硬化促進触媒であ
る。Catalysts for melamine derivative compounds used in combination here include polyvalent metal nitrates, halides, borofluorides, etc., such as zinc sulfate, aluminum nitrate, aluminum chloride, zinc borofluoride, tartaric acid, citric acid, ammonium tartrate, etc. These include inorganic or organic acids such as ammonium citrate and ammonium chloride, their ammonium salts, and mixed catalysts of salts and free acids such as phosphoric acid/ammonium chloride, which are all catalysts for accelerating the curing of melamine derivative compounds. It is.
使用量は、触媒の種類、メラミン誘導体化合物の種類に
よって異なるが9通常メラミン誘導体化合物の使用量に
対して10〜100%の範囲の処理液の濃度とし、使用
する。Although the amount used varies depending on the type of catalyst and the type of melamine derivative compound, the concentration of the treatment liquid is usually in the range of 10 to 100% of the amount of melamine derivative compound used.
本発明方法では、前述の第4級アンモニウム塩系抗菌剤
、メラミン誘導体化合物、メラミン誘導体化合物用触媒
の3種類を混合溶液とし、前述の布帛に含浸、乾燥し、
前述の付着量で第4級アンモニウム塩系抗菌剤とメラミ
ン誘導体化合物を布帛に付着させる。ここで布帛への含
浸は、吸尽法。In the method of the present invention, a mixed solution of the above-mentioned quaternary ammonium salt-based antibacterial agent, a melamine derivative compound, and a catalyst for melamine derivative compounds is impregnated into the above-mentioned fabric, dried,
The quaternary ammonium salt antibacterial agent and the melamine derivative compound are attached to the fabric in the above-mentioned amounts. The fabric is impregnated here using the exhaustion method.
パッド法、スプレー法等、従来から広く行われている公
知の方法でよく1本発明において特に限定しない。Well-known methods that have been widely used in the past, such as a pad method and a spray method, may be used, and the present invention is not particularly limited thereto.
本発明方法では、この後熱処理を行う。熱処理は、メラ
ミン誘導体化合物を硬化させるためのものであり2本発
明においては必須である。ここでの温度条件、処理時間
条件は、適宜選択すればよいが2通常処理温度は100
〜200℃の範囲。In the method of the present invention, heat treatment is then performed. The heat treatment is for curing the melamine derivative compound and is essential in the present invention. The temperature conditions and treatment time conditions here may be selected as appropriate; 2. The treatment temperature is usually 100
~200°C range.
処理時間は10〜600秒の範囲が好ましい。The treatment time is preferably in the range of 10 to 600 seconds.
(作 用)
本発明者らは、従来からよく知られているメラミン誘導
体化合物のもつ密着性の優れた被膜形成能に着目し、鋭
意検討した結果2本発明方法記載の付着量の範囲で付着
された第4級アンモニウム塩系抗菌剤とメラミン誘導体
化合物によって、染色堅牢度低下のない、洗濯耐久性に
優れた。抗菌性と良好な風合を有した布帛が得られるこ
とを見出した。(Function) The present inventors paid attention to the ability of the well-known melamine derivative compound to form a film with excellent adhesion, and as a result of intensive study, the results showed that 2. The quaternary ammonium salt-based antibacterial agent and melamine derivative compound provide excellent washing durability with no decrease in color fastness. It has been found that a fabric with antibacterial properties and good texture can be obtained.
本発明方法で得られた抗菌防臭布帛は、繊維表面に形成
されたメラミン誘導体化合物の被膜の厚みが、第4級ア
ンモニウム塩系抗菌剤のもつ長所である抗菌性を維持し
、また、短所である染色堅牢度低下を防止する最適な厚
みになっており、さらには、風合に対しても悪影響を及
ぼさない厚みになっている。The antibacterial and deodorizing fabric obtained by the method of the present invention maintains the antibacterial properties, which are the advantages of quaternary ammonium salt-based antibacterial agents, due to the thickness of the melamine derivative compound coating formed on the fiber surface, and also has the disadvantages of antibacterial properties. It has an optimal thickness that prevents a certain decrease in color fastness, and also has a thickness that does not adversely affect the texture.
(実施例)
以下、実施例によって本発明をさらに具体的に説明する
が、実施例における布帛の性能の測定。(Example) Hereinafter, the present invention will be explained in more detail with reference to Examples, including measurement of the performance of fabrics in Examples.
評価は1次の方法で行った。Evaluation was performed using the first method.
(1)染色堅牢度
■ 洗濯堅牢度
JIS L−0844(C−2法)
■ 摩擦堅牢度
JIS L−0849
(2)抗菌性(菌数測定法)
滅菌試料布に試験菌(ブドウ状球菌、 5taphyl
ococcus aureus I F O13277
)のブイヨン懸濁液を注加し、密閉容器中で37℃、1
8時間培養後の生菌数を計測し、無加工試料布に対する
増減値差を下記(1)式より求めた。(1) Color fastness ■ Washing fastness JIS L-0844 (C-2 method) ■ Rubbing fastness JIS L-0849 (2) Antibacterial property (bacteria count measurement method) Test bacteria (staphylococcus, 5taphyl
ococcus aureus I F O13277
) was added to the bouillon suspension, and the mixture was heated at 37°C for 1 hour in a closed container.
The number of viable bacteria after 8 hours of culture was measured, and the difference in increase/decrease value with respect to the unprocessed sample cloth was determined from the following formula (1).
A:無加工試料に接種した直後の菌数
B:無加工試料にて18時間培養した
後の菌数
C:加工試料にて18時間培養した後
の菌数
なお、試験に際しては、試験菌の活性状態を確認する必
要があり、 log(B/A) >2であればこの試験
を有効とみなすが、 log(B/A)≦2の場合には
、この試験を無効とみなして再試験を行う。A: Number of bacteria immediately after inoculating the unprocessed sample B: Number of bacteria after culturing the unprocessed sample for 18 hours C: Number of bacteria after culturing the processed sample for 18 hours. It is necessary to confirm the activation state; if log (B/A) > 2, this test is considered valid; however, if log (B/A) ≦ 2, this test is considered invalid and should be retested. I do.
〔3)洗濯方法
JIS L−0217103法
(4)風合
ハンドリングによる評価
O:良好 ×:硬い
実施例1
ポリエステル仮撚嵩高加工糸150デニール/48フイ
ラメントを用いて、3膜両面組織の九編地を編成し、精
練した後、下記処方1により、浴比1;30にて130
℃X30分間の染色を行った。[3) Washing method JIS L-0217103 method (4) Texture handling evaluation O: Good ×: Hard Example 1 Nine-knitted fabric with three-layer double-sided structure using polyester false-twisted bulky yarn 150 denier/48 filament After knitting and scouring, 130
Staining was carried out at ℃ for 30 minutes.
〔染色処方1]
酢酸 0.2cc/Il
得られた染色布を下記樹脂処方1の水溶液へ浸漬し、マ
ングルにて絞り率100%で絞った後。[Dyeing recipe 1] Acetic acid 0.2 cc/Il The obtained dyed cloth was immersed in an aqueous solution of resin recipe 1 below and squeezed with a mangle at a squeezing rate of 100%.
100℃で3分間乾燥した。It was dried at 100°C for 3 minutes.
〔樹脂処方1〕
ポリオキシエチレントリメチルアンモニウムクロライド
20g/II続いて、170℃にて30秒間
の熱処理を行い。[Resin formulation 1] Polyoxyethylene trimethyl ammonium chloride 20 g/II Subsequently, heat treatment was performed at 170° C. for 30 seconds.
本発明方法による抗菌防臭布帛を得た。An antibacterial and deodorizing fabric was obtained by the method of the present invention.
本発明との比較のため1本実施例において樹脂処方1の
水溶液への浸漬を省くほかは1本実施例と全く同一の方
法により比較用のブランクの布帛(比較例1)を得た。For comparison with the present invention, a comparative blank fabric (Comparative Example 1) was obtained in the same manner as in this Example except that immersion in the aqueous solution of Resin Formulation 1 was omitted.
また1本発明との比較のため1本実施例において用いた
樹脂処方1に代えて下記樹脂処方2.樹脂処方3.樹脂
処方4.樹脂処方5をそれぞれ用いるほかは1本実施例
と全く同一の方法により比較用の加工布帛(それぞれ比
較例2.比較例3゜比較例4.比較例5とする。)を得
た。In addition, for comparison with the present invention, the following resin formulation 2 was used instead of resin formulation 1 used in this example. Resin formulation 3. Resin formulation 4. Comparative processed fabrics (referred to as Comparative Example 2, Comparative Example 3, Comparative Example 4, and Comparative Example 5, respectively) were obtained in exactly the same manner as in this Example, except that Resin Formulation 5 was used in each case.
〔樹脂処方2〕
ポリオキシエチレントリメチルアンモニウムクロライF
20g/l〔樹脂処方3〕
スミテックスしジン M−33g/i
スミテックスアクセラレータ ACX
0.3g/l〔樹脂処方4〕
ポリオキシエチレントリメチルアンモニウムクロライF
20g/lスミテックスしジン M−30
,5g/lスミテックスアクセラレータ ACX
0.05g/!〔樹脂処方5〕
ポリオキシエチレントリメチルアンモニウムクロライド
20g/I!スミテックスしジン M−31
5g/fスミテックスアクセラし一タ ACX
1.5g/It上述のごとくして得られた
本発明および比較例1〜5の布帛の性能を測定、評価し
、その結果を合わせて第1表に示した。[Resin formulation 2] Polyoxyethylene trimethylammonium chloride F
20g/l [Resin formulation 3] Sumitex Shijin M-33g/i Sumitex Accelerator ACX
0.3g/l [Resin formulation 4] Polyoxyethylene trimethylammonium chloride F
20g/l Sumitex Shigin M-30
,5g/l Sumitex Accelerator ACX
0.05g/! [Resin formulation 5] Polyoxyethylene trimethyl ammonium chloride 20g/I! Sumitex Shigin M-31
5g/f Sumitex Axela Shichita ACX
1.5 g/It The performance of the fabrics of the present invention and Comparative Examples 1 to 5 obtained as described above was measured and evaluated, and the results are shown in Table 1.
第 1 表
第1表より明らかなように1本発明方法によって得られ
た抗菌防臭加工布帛は、染色堅牢度、抗菌性に優れてい
るとともに、良好な風合をも有した抗菌防臭加工布帛で
あった。Table 1 As is clear from Table 1, the antibacterial and deodorizing processed fabric obtained by the method of the present invention is an antibacterial and deodorizing processed fabric that has excellent color fastness and antibacterial properties, and also has a good texture. there were.
実施例2
経糸にポリエステル仮撚嵩高加工糸150デニール/3
0フイラメント、緯糸にポリエステル/綿(混率65/
35)の混紡糸40番手を用いて平組織の織物を製織し
、精練漂白した。Example 2 Warp: Polyester false twisted bulky yarn 150 denier/3
0 filament, weft polyester/cotton (mix ratio 65/
A plain weave fabric was woven using the blended yarn No. 40 of No. 35), and was scoured and bleached.
次に、下記染色処方2を用い、浴比1:30にて130
℃で30分間の染色を行い、布帛のポリエステル繊維サ
イドの染色を行った。Next, using the following dyeing recipe 2, dye 130% at a bath ratio of 1:30.
Dyeing was carried out at ℃ for 30 minutes to dye the polyester fiber side of the fabric.
〔染色処方2〕
DianixRed U−3E 1
% (ポリエステル糸)(三菱化成■製1分散染料)
重量比ニツカサンソルトRZ−8F 0.5g
/l酢酸 0.2cc/ 1
続いて、下記染色処方3を用い、浴比1:30゜染色温
度60℃、染色時間45分の条件にて綿糸サイドの染色
を行った後、 Kayafix CD (日本化薬■製
、ポリアミン系フィックス剤> 1g/lの濃度にて
、浴比1:30.処理温度60℃、処理時間20分の条
件で、綿糸サイドのフィックス処理を行った。[Dyeing prescription 2] DianixRed U-3E 1
% (Polyester thread) (Mitsubishi Kasei ■1 disperse dye)
Weight ratio Nitsuka Sunsalt RZ-8F 0.5g
/l acetic acid 0.2cc/1 Next, the cotton yarn side was dyed using dyeing recipe 3 below at a bath ratio of 1:30°, a dyeing temperature of 60°C, and a dyeing time of 45 minutes. Polyamine fixing agent manufactured by Kayaku ■ A fixing treatment was performed on the cotton yarn side at a concentration of 1 g/l, a bath ratio of 1:30, a treatment temperature of 60° C., and a treatment time of 20 minutes.
〔染色処方3〕
Mikacion Red GS 1%(綿
糸)(三菱化成ms、反応染料) 重量比無水
芒硝 10g/A炭酸ソーダ
10g/l得られた染色布を下記樹脂
処方6の水溶液へ浸漬して、マングルにて絞り率80%
で絞った後。[Dyeing recipe 3] Mikacion Red GS 1% (cotton thread) (Mitsubishi Kasei ms, reactive dye) Weight ratio anhydrous sodium sulfate 10g/A soda carbonate
The dyed cloth obtained at 10 g/l was immersed in an aqueous solution of resin formulation 6 below, and the squeezing rate was 80% with a mangle.
After narrowing down.
100℃で5分間の乾燥を行った。Drying was performed at 100°C for 5 minutes.
〔樹脂処方6〕
オクタデシルメチルベンジルアンモニウムクロライド
10g/J続いて、170℃にて30秒間の
熱処理を行い。[Resin formulation 6] Octadecylmethylbenzyl ammonium chloride
10g/J Subsequently, heat treatment was performed at 170°C for 30 seconds.
本発明方法による抗菌防臭布帛を得た。An antibacterial and deodorizing fabric was obtained by the method of the present invention.
本発明との比較のため1本実施例において樹脂処方6の
水溶液への浸漬を省くほかは9本実施例と全く同一の方
法により比較用のブランクの布帛(比較例6)を得た。For comparison with the present invention, a comparative blank fabric (Comparative Example 6) was obtained in the same manner as in this Example except that immersion in the aqueous solution of Resin Formulation 6 was omitted.
また2本発明との比較のだt55本実施において用いた
樹脂処方6に代えて下記樹脂処方7.樹脂処方8.樹脂
処方9.樹脂処方10をそれぞれ用いるほかは2本実施
例と全く同一の方法により比較用の加工布帛(それぞれ
比較例7.比較例8゜比較例9.比較例10とする。)
を得た。In addition, for comparison with the present invention, the following resin formulation 7 was used in place of resin formulation 6 used in this implementation. Resin formulation 8. Resin formulation9. Fabrics for comparison were processed in exactly the same manner as in the two examples except that resin formulation 10 was used respectively (Comparative Example 7, Comparative Example 8, Comparative Example 9, Comparative Example 10, respectively).
I got it.
〔樹脂処方7〕
オクタデシルメチルベンジルアン士ニウムクロライド
Log/l〔樹脂処方8〕
スミテックスレジン M−68g/A
スミテックスアクセラレータ ACX
3g/!〔樹脂処方9〕
オクタデシルメチルベンジルアンモニウムクロライF
10g/j!スミテックスレジン M−6
0,8g/Jスミテックスアクセラレータ ACX
0.3g/l〔樹脂処方10〕
オクタデシルメチ】Lベンジルアンモニウムクロライド
LOg/lスミテックスレジン M−62
0g/lスミテックスアクセラb−タ ACX
7g/l上述のごとくして得られた本
発明および比較例6〜10の布帛の性能を測定、評価し
、その結果を合わせて第2表に示した。[Resin formulation 7] Octadecylmethylbenzylaminium chloride
Log/l [Resin formulation 8] Sumitex Resin M-68g/A Sumitex Accelerator ACX
3g/! [Resin formulation 9] Octadecylmethylbenzylammonium chloride F
10g/j! Sumitex Resin M-6
0.8g/J Sumitex Accelerator ACX
0.3g/l [Resin formulation 10] Octadecylmethy] L benzyl ammonium chloride LOg/l Sumitex Resin M-62
0g/l Sumitex Accela b-ta ACX
The performance of the fabrics of the present invention and Comparative Examples 6 to 10 obtained as described above was measured and evaluated, and the results are shown in Table 2.
第
表
第2表より明らかなように9本発明方法によって得られ
た抗菌防臭加工布帛は、染色堅牢度、抗菌性に優れてい
るとともに、良好な風合をも有した抗菌防臭加工布帛で
あった。As is clear from Table 2, the antibacterial and deodorizing processed fabric obtained by the method of the present invention is an antibacterial and deodorizing processed fabric that has excellent color fastness and antibacterial properties, and also has a good texture. Ta.
(発明の効果)
本発明方法によって得られる抗菌防臭加工布帛は、染色
堅牢度に優れ、良好な風合を有し、洗濯耐久性に優れた
抗菌防臭性をも有している。(Effects of the Invention) The antibacterial and deodorizing treated fabric obtained by the method of the present invention has excellent color fastness, good hand feel, and antibacterial and deodorizing properties with excellent washing durability.
このように優れた性能を有する本発明の抗菌防臭加工布
帛は、衣料品、寝装品、インテリア品等に適した素材と
なる。The antibacterial and deodorizing treated fabric of the present invention having such excellent performance becomes a material suitable for clothing, bedding, interior goods, and the like.
特許l!:8願人 ユニチカ株式会社Patent l! :8 applicants Unitika Co., Ltd.
Claims (1)
誘導体化合物、メラミン誘導体化合物用触媒の3種類の
混合溶液を含浸し、該布帛の繊維重量に対して第4級ア
ンモニウム塩系抗菌剤を0.5〜5.0%、メラミン誘
導体化合物を0.1〜1.0%付着せしめ、しかる後に
乾燥、熱処理することを特徴とする染色堅牢度に優れた
抗菌防臭布帛の製造方法。(1) A fabric is impregnated with a mixed solution of three types of a quaternary ammonium salt antibacterial agent, a melamine derivative compound, and a catalyst for melamine derivative compounds, and the quaternary ammonium salt antibacterial agent is added to the fiber weight of the fabric. A method for producing an antibacterial and deodorizing fabric with excellent color fastness, characterized by depositing 0.5 to 5.0% and 0.1 to 1.0% of a melamine derivative compound, followed by drying and heat treatment.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2114467A JPH0411076A (en) | 1990-04-28 | 1990-04-28 | Production of antimicrobial and deodorizing fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2114467A JPH0411076A (en) | 1990-04-28 | 1990-04-28 | Production of antimicrobial and deodorizing fabric |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0411076A true JPH0411076A (en) | 1992-01-16 |
Family
ID=14638464
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2114467A Pending JPH0411076A (en) | 1990-04-28 | 1990-04-28 | Production of antimicrobial and deodorizing fabric |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0411076A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005054566A1 (en) | 2003-11-28 | 2005-06-16 | Arch Uk Biocides Limited | Fibres treated with antimicrobial agents |
JP2018071007A (en) * | 2016-10-24 | 2018-05-10 | 東洋紡Stc株式会社 | Antibacterial and antivirus processed fiber product |
-
1990
- 1990-04-28 JP JP2114467A patent/JPH0411076A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005054566A1 (en) | 2003-11-28 | 2005-06-16 | Arch Uk Biocides Limited | Fibres treated with antimicrobial agents |
US8147707B2 (en) | 2003-11-28 | 2012-04-03 | Arch Uk Biocides Limited | Fibres treated with antimicrobial agents |
JP2018071007A (en) * | 2016-10-24 | 2018-05-10 | 東洋紡Stc株式会社 | Antibacterial and antivirus processed fiber product |
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