JPS6020504B2 - Melt-proof processing method for synthetic fibers - Google Patents
Melt-proof processing method for synthetic fibersInfo
- Publication number
- JPS6020504B2 JPS6020504B2 JP1278578A JP1278578A JPS6020504B2 JP S6020504 B2 JPS6020504 B2 JP S6020504B2 JP 1278578 A JP1278578 A JP 1278578A JP 1278578 A JP1278578 A JP 1278578A JP S6020504 B2 JPS6020504 B2 JP S6020504B2
- Authority
- JP
- Japan
- Prior art keywords
- melt
- synthetic fibers
- fibers
- weight
- aqueous solution
- 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
- 229920002994 synthetic fiber Polymers 0.000 title claims description 20
- 239000012209 synthetic fiber Substances 0.000 title claims description 20
- 238000003672 processing method Methods 0.000 title claims description 4
- 238000000034 method Methods 0.000 claims description 23
- 239000007864 aqueous solution Substances 0.000 claims description 20
- 239000000835 fiber Substances 0.000 claims description 19
- -1 melamine derivative compound Chemical class 0.000 claims description 16
- 238000010438 heat treatment Methods 0.000 claims description 10
- 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 claims description 3
- 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 claims description 3
- 239000007787 solid Substances 0.000 claims description 2
- 239000004744 fabric Substances 0.000 description 19
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 238000002844 melting Methods 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 238000011161 development Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 229920000877 Melamine resin Polymers 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 230000002087 whitening effect Effects 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- 102000006835 Lamins Human genes 0.000 description 2
- 108010047294 Lamins Proteins 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000000986 disperse dye Substances 0.000 description 2
- 210000005053 lamin Anatomy 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- FSSPGSAQUIYDCN-UHFFFAOYSA-N 1,3-Propane sultone Chemical compound O=S1(=O)CCCO1 FSSPGSAQUIYDCN-UHFFFAOYSA-N 0.000 description 1
- UNPLRYRWJLTVAE-UHFFFAOYSA-N Cloperastine hydrochloride Chemical compound Cl.C1=CC(Cl)=CC=C1C(C=1C=CC=CC=1)OCCN1CCCCC1 UNPLRYRWJLTVAE-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-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
- 239000000980 acid dye Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- AIRPJJGSWHWBKS-UHFFFAOYSA-N hydroxymethylphosphanium;chloride Chemical compound [Cl-].OC[PH3+] AIRPJJGSWHWBKS-UHFFFAOYSA-N 0.000 description 1
- 239000006193 liquid solution Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
【発明の詳細な説明】
本発明は合成繊維の防融加工法に係り、詳しくは、メラ
ミン誘導体化合物を用いて合成繊維に防融性を付与する
為の改良された方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for melt-proofing synthetic fibers, and more particularly to an improved method for imparting melt-proofing properties to synthetic fibers using a melamine derivative compound.
従来、メラミン誘導体化合物を用いて合成繊維に防融性
を付与する方法としては、合成繊維にメラミン誘導体化
合物と酸性触媒とを含む液を施与した後水分の存在下で
加熱処理する方法(特公昭48一1247計号公報)あ
るいは合成繊維にメラミン誘導体化合物とテトラキスヒ
ドロキシメチルホスホニゥムクロラィド又はプロパンサ
ルトンとを含む液を施与した後蒸熱処理する方法(侍関
昭50−13650び号公報)等が公知である。しかし
ながらこれらの方法では合成繊維に十分なる防敵性を付
与しようとすれば、メラミン誘導体化合物を繊維に対し
て1の重量%程度以上付着せしめる必要があり、このよ
うに多量の樹脂付着量とすると、彼染物の場合には色相
がくすみ、発色性、鮮明性が低下して商品価値が著しく
低下するという欠点があって実用化は極めて困難である
。これに対して、処理液中に界面活性剤を共存せしめる
か、もしくは予め合成繊維表面を薬剤処理することによ
ってメラミン樹脂付着状態の均質化を計り、所要樹脂量
を5重量%以下、1〜4重量%程度に低減せしめる方法
(特公昭49−32760号公報)が提案されているが
、この方法によれば、色相の鮮明性、発色性の低下はあ
る程度防げるもの)未だ不充分であり実用性に乏しいの
みならず樹脂童が十分でない為、必ずしも満足すべき防
融効果は得られないという難点がある。Conventionally, methods for imparting melt-proofing properties to synthetic fibers using melamine derivative compounds include applying a solution containing a melamine derivative compound and an acidic catalyst to synthetic fibers and then heat-treating them in the presence of moisture (specifically, Publication No. 1247 of 1973) or a method of applying a liquid containing a melamine derivative compound and tetrakis hydroxymethylphosphonium chloride or propane sultone to synthetic fibers and then steam-treating them (No. 13650 of Samurai Seki No. 13650) Publications) etc. are publicly known. However, with these methods, in order to impart sufficient enemy resistance to synthetic fibers, it is necessary to attach the melamine derivative compound to the fibers in an amount of about 1% by weight or more, and when such a large amount of resin is attached, In the case of dyed products, the hue becomes dull, the color development and sharpness are reduced, and the commercial value is significantly reduced, making it extremely difficult to put it into practical use. On the other hand, by coexisting a surfactant in the treatment solution or treating the surface of synthetic fibers with chemicals in advance, the melamine resin adhesion state was homogenized, and the required amount of resin was reduced to 5% by weight or less, 1 to 4% by weight. A method has been proposed (Japanese Patent Publication No. 49-32760) to reduce the amount by weight, but this method (although it can prevent the deterioration of hue clarity and color development to some extent) is still insufficient and impractical. The problem is that not only is there a lack of resin, but also there is not enough resin, so a satisfactory anti-melting effect cannot necessarily be obtained.
さらに、合成繊維を予め薬剤で処理する場合にあっては
、二段処理である為操作が大変煩雑であり、又処理条件
によっては繊維物性が低下することがある。加えて以上
いずれの方法に於ても、酸性触媒の存在下に加熱処理を
行う為、メラミン誘導体化合物からホルマリンが遊離し
て、作業環境を汚染したり、被処理物に吸着残存して衛
生上好ましからざる影響を与えるといいう重大な欠点が
ある。本発明者等は、以上のような合成繊維の防融加工
上の諸問題を解決する為鋭意研究の結果本発明を完成し
た。即ち本発明の目的は着色合成繊維の発色性、鮮明性
を損うことなく、これにすぐれた防融性を付与する方法
を提供することにある。Furthermore, when synthetic fibers are pretreated with chemicals, the two-stage treatment is very complicated, and depending on the treatment conditions, the physical properties of the fibers may deteriorate. In addition, in all of the above methods, since heat treatment is performed in the presence of an acidic catalyst, formalin is liberated from the melamine derivative compound, contaminating the working environment, and adsorbing and remaining on the object to be treated, resulting in sanitary issues. It has the serious drawback of having undesirable effects. The present inventors completed the present invention as a result of intensive research in order to solve the above-mentioned problems in melt-proofing processing of synthetic fibers. That is, an object of the present invention is to provide a method for imparting excellent melt resistance to colored synthetic fibers without impairing their color development and vividness.
本発明の他の目的は、メラミン譲導体化合物を用いて合
成繊維に防融性を付与するに際して、遊離ホルマリンの
発生が抑止され、作業環境並に製品の衛生性の改善され
た方法を提供することにある。本発明のさらに他の目的
並に効果は以下に述べるところから明らかとなろう。Another object of the present invention is to provide a method in which the production of free formalin is suppressed when imparting melt-proofing properties to synthetic fibers using a melamine transfer compound, thereby improving the working environment and the hygiene of the product. There is a particular thing. Further objects and effects of the present invention will become apparent from the following description.
上記の目的は、合成繊維に、メラミン誘導体化合物を含
むpH8.5〜10.0の水溶液を施与し次いで繊維重
量に対して25%以上の水分の存在下に湿熱処理を施す
ことを特徴とする合成繊維の防融加工法によって蓬せら
れる。The above object is characterized by applying an aqueous solution containing a melamine derivative compound with a pH of 8.5 to 10.0 to synthetic fibers, and then subjecting the synthetic fibers to a moist heat treatment in the presence of a moisture content of 25% or more based on the weight of the fibers. It has been made popular by the melt-proof processing method for synthetic fibers.
本発明方法によれば、メラミン誘導体化合物の繊維に対
する付着量が例えば5重量%を超えて多くなっても彼染
物が白化して色相にくすみを生ずることがなく、防葛虫
性と色相の発色性、鮮明性とを兼ね具えた製品を得るこ
とが出釆る。According to the method of the present invention, even if the amount of the melamine derivative compound attached to the fiber increases, for example, in excess of 5% by weight, the dyed material will not whiten and the hue will become dull, and the dyed material will not become white and the hue will develop. It is possible to obtain a product that has both color and clarity.
本発明で云う合成繊維としては、ポリアミド繊維、ポリ
エステル繊維、ポリアクリロニトリル繊維、ポリオレフ
ィン繊維などがあり、これらは、綿、糸、縄織物、不織
布等任意の形状で用いることができる。又これら合成繊
維は相互にもしくは天然繊維などの非熱溶融性繊維と、
混紡、交織或は交緩されていてもよい。The synthetic fibers referred to in the present invention include polyamide fibers, polyester fibers, polyacrylonitrile fibers, polyolefin fibers, and the like, and these can be used in any form such as cotton, thread, rope fabric, and nonwoven fabric. In addition, these synthetic fibers can be mixed with each other or with non-heat meltable fibers such as natural fibers.
It may be blended, interwoven or interlaced.
本発明で用いるメラミン譲導体化合物としては例えばへ
キサメチロールメラミン、トリ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、ヘキサキスメトキシ
メチロールメラミン等が挙げられるがこれらに限定され
るものではない。これらメラミン誘導体化合物のうちで
も、ヘキサメチロールメラミン及びトリメチロールメラ
ミンは、特にすぐれた防融効果を与え、しかも樹脂化速
度が速い、製造もしくは入手が容易であるなどの利点も
あって、本発明に好適に用い鶴るものである。これらメ
ラミン誘導体化合物を含む水溶液中の該化合物の濃度は
、一般に1〜4の重量%、好ましくは5〜25重量%の
範囲である。Examples of the melamine transfer compound used in the present invention include, but are not limited to, hexamethylolmelamine, trimethylolmelamine, trismethoxymethylolmelamine, hexakismethoxymethylolmelamine, and the like. Among these melamine derivative compounds, hexamethylol melamine and trimethylol melamine have particularly excellent anti-melting effects, and also have advantages such as fast resin formation rate and easy production or acquisition, and are therefore used in the present invention. It is suitable for use. The concentration of these melamine derivative compounds in aqueous solutions generally ranges from 1 to 4% by weight, preferably from 5 to 25% by weight.
又、本発明に於ては、上記水溶液のpHが8.5〜10
.0の範囲内にあることが特り重要であり、pHが8.
5を下廻われば、防融効果は得られるもの被染物の場合
には白化が生じて色相の発色性、鮮明性が低下し、又一
般的にも遊離ホルマリンの発生を抑止することが困難と
なり、逆に10.0を上廻わればメラミン誘導体化合物
の樹脂化に長時間を要して良好な防融性は得難くいずれ
も本発明の目的を達し得ないo水溶液のpHの調整には
、苛性ソーダ、苛性カリ、ソーダ灰、アンモニア、トリ
ェタノールアミン、ジメチルアミノェタノールなど無機
、有機を問わず塩基性物質のいずれもが使用可能である
が、一般には、苛性アルカリもしくは塩基性無機塩を使
用するのが操作が簡便であって好ましい。Further, in the present invention, the pH of the aqueous solution is 8.5 to 10.
.. It is particularly important that the pH is within the range of 8.
If the value is less than 5, the anti-melting effect can be obtained, but in the case of dyed items, whitening occurs and the color development and clarity of the hue decreases, and it is generally difficult to suppress the generation of free formalin. On the other hand, if it exceeds 10.0, it will take a long time to turn the melamine derivative compound into a resin, making it difficult to obtain good melt resistance, and in either case, the purpose of the present invention cannot be achieved. Any basic substance, whether inorganic or organic, such as , caustic soda, caustic potash, soda ash, ammonia, triethanolamine, dimethylaminoethanol, etc., can be used, but in general, caustic alkali or basic inorganic salts are used. It is preferable to do this because the operation is simple.
又、上記〆ラミン誘導体化合物を含む水溶液中には、該
化合物の樹脂化を助ける意味で8−ヒドロキシエチルテ
レフタレート、ジメチルフタレート、尿素、チオ尿素、
トIJアゾン化合物などを添加しても良く、さらに非イ
オン界面活性剤等を共存せしめてメラミン誘導体化合物
の繊維表面への付着性を改善せしめることもできる。但
し、8−ヒドロキシェチルテレフタレートなどを用いる
場合は、その添加量があまりに多くなりすぎれば、被染
物の色相にくすみを生ずることがあるので、一般には水
溶液中1重量%以下、好ましくは0.5重量%以下とす
るのがよい。又、非イオン界面活性剤等を用いる場合に
は、水溶液中0.001〜0.1重量%程度の濃度とす
る。上記〆ラミン誘導体化合物を含む水溶液を合成繊維
に施与する為の手段としては、パッド法、浸漬法、贋霧
法、塗布法など通常繊維加工に用いられる手段のいずれ
もが使用可能であるが、均一施与の観点からは一般にパ
ット法を用いるのが良い。In addition, in the aqueous solution containing the above lamin derivative compound, 8-hydroxyethyl terephthalate, dimethyl phthalate, urea, thiourea,
In addition, a nonionic surfactant or the like may be added to improve the adhesion of the melamine derivative compound to the fiber surface. However, when using 8-hydroxyethyl terephthalate or the like, if the amount added is too large, the hue of the dyed object may become dull. The content is preferably 5% by weight or less. When a nonionic surfactant or the like is used, the concentration in the aqueous solution is approximately 0.001 to 0.1% by weight. As a means for applying the aqueous solution containing the above-mentioned lamin derivative compound to synthetic fibers, any of the means normally used for fiber processing, such as a pad method, dipping method, mist method, coating method, etc., can be used. From the viewpoint of uniform application, it is generally better to use the pad method.
施与量は、繊維重量に対して、メラミン譲導体固形分で
2〜30%、好ましくは3〜15%である。施与量が2
%を下廻われば、十分なる防融効果を得ることが困難で
あり、又一方30%を上廻われば彼処理物の風合が粗剛
となるばかりでなく、色相のくすみが生ずることがあっ
て好ましくない。上記水溶液施与が終ったならば、次い
で被処理物に湿熱処理を施す。The application amount is from 2 to 30%, preferably from 3 to 15%, based on the weight of the fibers, in solids content of the melamine derivative. The dosage is 2
If it is less than 30%, it is difficult to obtain a sufficient anti-melting effect, while if it is more than 30%, not only will the texture of the treated product become rough and stiff, but the hue may become dull. I don't like it. After the application of the aqueous solution is completed, the object to be treated is then subjected to a moist heat treatment.
ここで本発明に於ては、被処理物やその繊維重量に対し
て25%以上の水分を保持していることが肝要であって
、これを下廻われば目的の防融効果を得ることが出釆な
い。従って一般には、被処理物に水溶液を施与し、必要
に応じて鮫液した後、予備乾燥工程等を経ることなく直
ちに緑熱処理を行うのがよく、か)る方法を用いれば、
工程を簡略化できるという利点もある。湿熱処理は、温
度60〜180qo、好ましくは95〜140℃で相対
湿度40%以上、好ましくは95%以上の条件下で行わ
れる。Here, in the present invention, it is important to retain 25% or more moisture based on the weight of the material to be treated and its fibers, and if this is lowered, the desired anti-melting effect can be obtained. is not available. Therefore, in general, it is best to apply an aqueous solution to the object to be treated and, if necessary, apply a liquid solution, and then immediately perform the green heat treatment without going through a preliminary drying process.
Another advantage is that the process can be simplified. The moist heat treatment is performed at a temperature of 60 to 180 qo, preferably 95 to 140°C, and a relative humidity of 40% or more, preferably 95% or more.
処理時間はメラミン誘導体化合物の種類、水溶液の初期
pH、処理温度等によって異なるが、一般には10〜1
8の分程度である。以上の処理を終ったならば、次いで
常法に従ってソーピング、水洗、乾燥、仕上セットを行
って最終製品とするが、必要とあらば、該仕上セット時
に、帯電防止剤或は柔軟剤等を施与してもよい。かくし
て本発明によれば、被処理物に対するメラミン譲導体化
合物の付着量が大となっても色相にくすみを生ずること
がなく、すぐれた防融性と色相の鮮明性、発色性とを兼
ね具えた合成繊維製品を得ることが可能であり、又処理
工程中に於ける遊離ホルマリンの発生が極めて少ないの
で作業環境が改善されると共に製品の衛生性も向上する
のである。The treatment time varies depending on the type of melamine derivative compound, the initial pH of the aqueous solution, the treatment temperature, etc., but is generally 10 to 1
It is about 8 minutes. Once the above treatment is completed, the final product is prepared by soaping, washing, drying, and final setting according to conventional methods.If necessary, antistatic agents or softeners may be applied during finishing setting. may be given. Thus, according to the present invention, even if the amount of the melamine transfer compound attached to the object to be treated is large, the hue does not become dull, and it has excellent melt resistance, clear hue, and color development. Furthermore, since the generation of free formalin during the treatment process is extremely low, the working environment is improved and the hygiene of the product is also improved.
さらに処理が弱アルカリ性の温和な条件で行われる為、
被処理物の物性が据われることがないのも本発明の利点
であり、その工業的利用価値は極めて大きい。以下実施
例によって本発明をさらに具体的に説明する。Furthermore, since the treatment is carried out under mild alkaline conditions,
Another advantage of the present invention is that the physical properties of the object to be treated are not determined, and its industrial utility value is extremely large. The present invention will be explained in more detail below with reference to Examples.
なお、実施列中、樹脂付着率(%)は、処理布の重量増
加より算出し、色相変化は日立自記分光光度計EPR−
2型により頚。色した時の処理布と未処理布の色差△E
を以て示した。又、防融性は、所定の温度に保持した直
径7の‘の銅棒に5仇×5地の試験布を無荷重(自重)
で5秒間接鮫させ、接触部が溶融して穴があくかどうか
を肉眼で判定した。実施例 1
目付2502/〆のポリエステル加工糸綾織物ッイルを
分散染料を用い常法によりネービープル一に染色した。In addition, in the experiment, the resin adhesion rate (%) was calculated from the weight increase of the treated cloth, and the hue change was calculated using the Hitachi self-recording spectrophotometer EPR-
Type 2 causes neck. Color difference △E between treated fabric and untreated fabric when colored
This is shown below. In addition, the melt resistance is measured by placing a test cloth of 5 pieces x 5 pieces on a copper rod with a diameter of 7' held at a predetermined temperature with no load (self weight).
for 5 seconds, and visually judged whether the contact area melted and formed a hole. Example 1 A polyester processed yarn twill fabric with a basis weight of 2502/m2 was dyed in a navy blue color using a disperse dye in a conventional manner.
この彼染物に第1表に示した組成の水溶液を10の重量
%(対繊維)均一にパッド法により付着させ乾燥させる
ことなく相対湿度98%温度103午0の加熱蒸気中で
90分間の虚熱処理を行い、しかる後未反応物を非イオ
ン界面活性剤2夕/そを用い80℃で20分間のソーピ
ングにより洗浄除去し乾燥後帯電防止剤を付与した。得
られた処理布について樹脂付着率、色差△E、及び防融
性を測定し第1表の如き結果を得た。なお、上記操作中
、水溶液施与後、110ooで予備乾燥を行って、被染
物の水分保持率を約20%(対繊維重量)とした後湿熱
処理を行ったものは、防融試験に於て300午○以下で
溶融開孔し、処理効果は殆んど得られなかった。An aqueous solution having the composition shown in Table 1 was uniformly applied to this dyed material by a pad method in an amount of 10% by weight (based on the fibers), and it was evaporated for 90 minutes in heated steam at a relative humidity of 98% and a temperature of 103:00 without drying. A heat treatment was carried out, and then unreacted substances were washed and removed by soaping at 80° C. for 20 minutes using two coats of a nonionic surfactant, and after drying, an antistatic agent was applied. The resin adhesion rate, color difference ΔE, and melt resistance of the obtained treated cloth were measured, and the results shown in Table 1 were obtained. In addition, during the above operation, after applying the aqueous solution, pre-drying at 110 oo to make the moisture retention rate of the dyed material about 20% (based on the weight of the fiber), followed by moist heat treatment, did not pass the anti-melt test. Melting occurred at less than 300 pm, and almost no treatment effect was obtained.
又、pH9.7の水溶液を用いた場合(本発明例)に於
ける操作中のホルマリン臭の発生は、低いpHの水溶液
、特にpH6.4の場合に比しかるかに少なかつた。Furthermore, when an aqueous solution with a pH of 9.7 was used (the example of the present invention), the occurrence of formalin odor during operation was much less than when an aqueous solution with a low pH, especially an aqueous solution with a pH of 6.4, was used.
第 1 表
任 ■ べッカミンJIOI(大日本イン布機製)■ク
ーヒドロキンェチルテレフタレート第1表に示した如く
、水溶液の母が8.5を下廻わる場合(比較例1、2、
3)には処理布と未処理布との色差△Eが大となるのに
対し、pH9.7の水溶液を用いた本発明例(4、5)
では色相変化が極めて少なく、しかも防融性は酸性処理
液を用いる方法と同様すぐれている。1st Representation ■ Beccamin JIOI (manufactured by Dainippon Inn Cloth Machinery Co., Ltd.) ■ Cuhydroquinethyl terephthalate As shown in Table 1, when the aqueous solution has a concentration of less than 8.5 (Comparative Examples 1, 2,
In 3), the color difference ΔE between the treated fabric and the untreated fabric is large, whereas inventive examples (4, 5) using an aqueous solution with a pH of 9.7
With this method, there is very little change in hue, and the melting resistance is as good as that of the method using an acidic treatment liquid.
色差に関しては、一般に△Eが1以下であれば見た目で
殆んど色差を感じないとされており、事実比較例で得ら
れた処理布には明らかに白化が認められたが、本発明例
では処理布と未処理布の色差は肉眼的には殆んど識別で
きなかった。一方pHが10を上廻る場合(比較例6)
には色相の変化が少なく、色相の鮮明性、発色性にはす
ぐれているが、防融効果は殆んど得られず本発明の目的
を達し得ない。Regarding color difference, it is generally said that if ΔE is 1 or less, there is almost no visible color difference.In fact, whitening was clearly observed in the treated cloth obtained in the comparative example, but in the present invention example, whitening was clearly observed. The color difference between the treated and untreated fabrics was almost invisible to the naked eye. On the other hand, when the pH is over 10 (Comparative Example 6)
Although the change in hue is small and the vividness of the hue and color development are excellent, the anti-melting effect is hardly obtained and the object of the present invention cannot be achieved.
尚、本発明の処理布は、家庭洗濯或はドライクリーニン
グを各1の司以上行った後にも初期の性能を保持してお
り、風合もよく、商品価値の高いものであった。The treated fabric of the present invention retained its initial performance even after being washed at home or dry cleaned one or more times, had a good feel, and had high commercial value.
実施例 2
目付270夕/淋のポリエステル織物バックッィルアム
ンゼンを分散染料を用いて常法によりコーヒーブラウン
に染色した。Example 2 A polyester fabric with a fabric weight of 270/yel was dyed coffee brown by a conventional method using a disperse dye.
この被染物に第2表に示した組成の水溶液を115重量
%均一にパッド法により付着させ以下実施例1と同様に
処理した。115% by weight of an aqueous solution having the composition shown in Table 2 was uniformly applied to this dyed object by the pad method, and the treatment was then carried out in the same manner as in Example 1.
得られた処理布の諸物性を第2表に示した。Table 2 shows the physical properties of the treated fabric obtained.
第 2 表任 @ べッカミンPMし大日本インキ■製
)第2表よりpH8.7のアルカリ性水溶液を用いた場
合は、色相の変化が少なく色彩効果にすぐれしかも防融
性の良好な製品が得られることがわかる。尚ここで得ら
れた本発明の処理布は、風合も良好であり、商品価値の
高いものであった。実施例 3目付155夕/めのナイ
ロン6織物を酸性染料を用いて常法により鮮明なブルー
に染色した。From Table 2, when using an alkaline aqueous solution with a pH of 8.7, a product with less change in hue, excellent color effects, and good melt resistance can be obtained. I know that it will happen. The treated fabric of the present invention obtained here had a good feel and had high commercial value. Example 3 A nylon 6 fabric with a fabric weight of 155 mm/m was dyed a vivid blue using an acid dye in a conventional manner.
この被染物に第3表に示した組成の水溶液を7丸重量%
均一にパッド法により付着させ以下実施例1と同じ様に
処理した。得られた処理布の諸物性を第3表に示した。Add 7% by weight of an aqueous solution having the composition shown in Table 3 to this dyed object.
It was uniformly deposited by the pad method and treated in the same manner as in Example 1. Table 3 shows the physical properties of the treated fabric obtained.
第 3 表圧Q実施例IK同じ酸性が一層改善されるこ
とがわかる。3rd Surface Pressure Q Example IK It can be seen that the same acidity is further improved.
又、ナイロンの場合には、被染物は特に鮮明な色相を有
するので、.△Eが1以上となる比較例では商品価値が
著しく低下する。In addition, in the case of nylon, the dyed material has a particularly vivid hue. In comparative examples where ΔE is 1 or more, the commercial value decreases significantly.
Claims (1)
5〜10.0の水溶液を施与し、次いで繊維重量に対し
て25%以上の水分の存在下に湿熱処理を施すことを特
徴とする合成繊維の防融加工法。 2 メラミン誘導体化合物が、トリメチロールメラミン
もしくはヘキサメチロールメラミンである特許請求の範
囲第1項に記載の防融加工法。 3 メラミン誘導体化合物を繊維重量に対して固形分で
3〜15%施与する特許請求の範囲第1項又は第2項に
記載の防融加工法。 4 湿熱処理を温度60℃〜180℃、相対湿度40%
以上の加熱雰囲気中で行う特許請求の範囲第1項に記載
の防融加工法。[Claims] 1 Synthetic fiber containing a melamine derivative compound at pH 8.
A method for melt-proofing synthetic fibers, which comprises applying an aqueous solution of 5 to 10.0% and then subjecting the fibers to a moist heat treatment in the presence of a moisture content of 25% or more based on the weight of the fibers. 2. The melt-proofing method according to claim 1, wherein the melamine derivative compound is trimethylolmelamine or hexamethylolmelamine. 3. The melt-proof processing method according to claim 1 or 2, wherein the melamine derivative compound is applied in a solid content of 3 to 15% based on the weight of the fiber. 4 Moist heat treatment at a temperature of 60°C to 180°C and a relative humidity of 40%.
The melt-proof processing method according to claim 1, which is carried out in the above heating atmosphere.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1278578A JPS6020504B2 (en) | 1978-02-06 | 1978-02-06 | Melt-proof processing method for synthetic fibers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1278578A JPS6020504B2 (en) | 1978-02-06 | 1978-02-06 | Melt-proof processing method for synthetic fibers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54106699A JPS54106699A (en) | 1979-08-21 |
| JPS6020504B2 true JPS6020504B2 (en) | 1985-05-22 |
Family
ID=11815041
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1278578A Expired JPS6020504B2 (en) | 1978-02-06 | 1978-02-06 | Melt-proof processing method for synthetic fibers |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6020504B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57180767U (en) * | 1981-05-12 | 1982-11-16 |
-
1978
- 1978-02-06 JP JP1278578A patent/JPS6020504B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54106699A (en) | 1979-08-21 |
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