JP2006214039A - Oil agent for cellulosic fibers and method for producing cellulosic fiber product using the oil agent and having rich elasticity and flexibility - Google Patents

Oil agent for cellulosic fibers and method for producing cellulosic fiber product using the oil agent and having rich elasticity and flexibility Download PDF

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JP2006214039A
JP2006214039A JP2005028396A JP2005028396A JP2006214039A JP 2006214039 A JP2006214039 A JP 2006214039A JP 2005028396 A JP2005028396 A JP 2005028396A JP 2005028396 A JP2005028396 A JP 2005028396A JP 2006214039 A JP2006214039 A JP 2006214039A
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oil agent
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JP3966881B2 (en
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Shojin Lee
承仁 李
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Abstract

<P>PROBLEM TO BE SOLVED: To provide an oil agent which enables the production of cellulosic fiber products having rich elasticity and flexibility and is friendly for the environments. <P>SOLUTION: This oil agent for the cellulosic fibers is characterized by containing a mixture solution of a polyoxyethylene ether type surfactant with an alkyl polyamine derivative cation surfactant, and an acetic dimethylol urea in a weight ratio of 0.6 to 50 : 1 in acidic water. The method for producing a cellulosic fiber product holding elasticity and flexibility in good durability comprises subjecting the cellulosic fiber product to an immersion or penetration-dispersing treatment in an acidic aqueous oil agent containing 0.1 to 0.4 wt.% of a mixture solution of a polyoxyalkylene ether surfactant with an alkyl polyamine derivative cation surfactant and 0.008 to 0.018 wt.% of an acetic dimethylol urea, dehydrating the treated cellulosic fiber product, and then drying the dehydrated product at 83°C. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

本発明は、セルロース系繊維処理用の新規な油剤及びそれを使用した弾力性及び柔軟性に富んだセルロース系繊維製品の製造方法に関する。 The present invention relates to a novel oil agent for treating cellulosic fibers and a method for producing a cellulosic fiber product having high elasticity and flexibility using the same.

通常セルロース系フィラメントは、油剤処理をし、乾燥するが、ケーキの外側と内側の収縮差が不均一であるため内外繊度差が発生する欠点があった。そこで、本発明者は、油剤としてコーンオイルとポリオキシエチレンアルキルエーテル型界面活性剤とアルキレンポリアミン誘導体の陽イオン界面活性剤と尿素系樹脂と樹脂化触媒を併用する方法を開発した(特許文献1参照)。この方法では、フィラメントの膨潤度を低め、乾燥の進行に伴う自由収縮を可能とし、繊度が均一で、表面が平滑な製品を得る事が可能となった。
特公昭64−3987号公報
Usually, cellulose-based filaments are treated with an oil agent and dried. However, the difference in shrinkage between the outer side and the inner side of the cake is non-uniform, so that there is a disadvantage that a difference in inner and outer fineness occurs. Therefore, the present inventor has developed a method in which corn oil, a polyoxyethylene alkyl ether type surfactant, an alkylene polyamine derivative cationic surfactant, a urea resin, and a resin catalyst are used in combination as an oil agent (Patent Document 1). reference). In this method, the degree of swelling of the filament is reduced, free shrinkage is possible with the progress of drying, and a product having a uniform fineness and a smooth surface can be obtained.
Japanese Patent Publication No. 64-3987

本発明は、かかる従来の方法を更に改良し、弾力性及び柔軟性に富んだセルロース系繊維製品の製造を可能とする、環境に優しい新規な油剤を提供することを課題とする。 It is an object of the present invention to provide a new environmentally friendly oil agent that can further improve such a conventional method and enables production of a cellulosic fiber product rich in elasticity and flexibility.

本発明では、下記組成からなる油剤を調製することにより、上記課題を解決した。
すなわち、酸性水中に、ポリオキシエチレンエーテル型の界面活性剤とアルキルポリアミン誘導体の陽イオン界面活性剤との混合液と、アセチックジメチロール尿素を重量比率で0.6〜50:1の割合で含有するものをセルロース系繊維用油剤とする。
In this invention, the said subject was solved by preparing the oil agent which consists of the following composition.
That is, a mixture of a polyoxyethylene ether type surfactant and an alkyl polyamine derivative cationic surfactant and an acetic dimethylolurea in acidic water at a weight ratio of 0.6 to 50: 1. What is contained is an oil for cellulosic fibers.

油剤は、濃度を変化させて使用可能であるが、通常、セルロース系繊維を処理する時の成分比率は、酸性水中に、ポリオキシエチレンエーテル型の界面活性剤とアルキルポリアミン誘導体の陽イオン界面活性剤との混合液0.1〜0.4重量%と、アセチックジメチロール尿素0.008〜0.018重量%を含有するのがよい。 Oil agents can be used at different concentrations, but the component ratio when treating cellulosic fibers is usually the cationic water activity of polyoxyethylene ether type surfactant and alkyl polyamine derivative in acidic water. It is good to contain 0.1-0.4 weight% of liquid mixture with an agent, and 0.008-0.018 weight% of acetyl dimethylol urea.

なお、上記ポリオキシエチレンアルキルエーテル型の界面活性剤とアルキルポリアミン誘導体の陽イオン界面活性剤との混合重量比率が1:1〜1:5程度でよく、特に1:1.25程度であるのがよい。 The mixing weight ratio of the polyoxyethylene alkyl ether type surfactant and the alkyl polyamine derivative cationic surfactant may be about 1: 1 to 1: 5, and particularly about 1: 1.25. Is good.

本発明で使用するポリオキシエチレンエーテル型の界面活性剤としては、例えば松本油脂製薬製のActinol-R-100が、またアルキルポリアミン誘導体の陽イオン界面活性剤としては、例えば松本油脂製薬製のZONTES-TA-460-15が例示できる。使用時の油剤中、ポリオキシエチレンエーテル型の界面活性剤とアルキルポリアミン誘導体の陽イオン界面活性剤との混合液の重量は0.1〜0.4重量%であればよいが、通常0.25〜0.3重量%程度であるのが好ましい。これら界面活性剤の併用により、アセチックジメチロール尿素のセルロース系繊維への浸透分散性が高められ、架橋結合が効率よく生じ、所望の製品を得ることができるのである。 Examples of the polyoxyethylene ether type surfactant used in the present invention include Actinol-R-100 manufactured by Matsumoto Yushi Seiyaku, and examples of cationic surfactants for alkylpolyamine derivatives include ZONTES manufactured by Matsumoto Yushi Seiyaku. -TA-460-15 can be exemplified. The weight of the mixed liquid of the polyoxyethylene ether type surfactant and the alkyl polyamine derivative cationic surfactant in the oil used may be 0.1 to 0.4% by weight. It is preferably about 25 to 0.3% by weight. By using these surfactants in combination, the osmotic dispersibility of the acetic dimethylolurea into the cellulosic fibers is enhanced, cross-linking occurs efficiently, and a desired product can be obtained.

次に、本発明で使用するアセチックジメチロール尿素は、酢酸とジメチロール尿素から得られる、ジメチロール尿素の酢酸エステルである。 Next, the acetic dimethylol urea used in the present invention is an acetic acid ester of dimethylol urea obtained from acetic acid and dimethylol urea.

Figure 2006214039
Figure 2006214039

このアセチックジメチロール尿素が繊維の分子C−OHのOH基に素早く作用し、繊維に沢山の架橋結合を生じ、弾力性を増すのである。 This acetic dimethylol urea acts quickly on the OH group of the fiber molecule C 6 H 9 O 4 —OH, causing a lot of cross-linking in the fiber and increasing the elasticity.

Figure 2006214039
Figure 2006214039

アセチックジメチロール尿素の使用量は使用時の油剤中0.008〜0.018重量%程度でよいが、通常0.006〜0.012重量%であるのがよい。 The amount of acetic dimethylol urea used may be about 0.008 to 0.018% by weight in the oil during use, but usually 0.006 to 0.012% by weight.

このような本発明の油剤を使用してセルロース系繊維製品を処理することにより、弾力性及び柔軟性をセルロース系繊維製品に付与できるが、その方法は、例えばポリオキシアルキルエーテル界面活性剤とアルキルポリアミン誘導体の陽イオン界面活性剤との混合液0.1〜0.4重量%とアセチックジメチロール尿素0.008〜0.018重量%を含有する酸性の水性油剤に浸漬或いは浸透させ、脱水後、83℃以上(好ましくは85℃前後)で乾燥するというものである。 By treating a cellulosic fiber product using such an oil agent of the present invention, elasticity and flexibility can be imparted to the cellulosic fiber product. Immersion or penetration into an acidic aqueous oil containing 0.1 to 0.4% by weight of a mixed solution of a polyamine derivative with a cationic surfactant and 0.008 to 0.018% by weight of acetic dimethylolurea, followed by dehydration Then, drying is performed at 83 ° C. or higher (preferably around 85 ° C.).

脱水後の乾燥工程は、セルロース系フィラメントは通常のトンネル乾燥機などによってのよいが、ビスコースステーブルファイバーは、油剤処理及び脱水処理をした製品を通気性ある袋に入れて、袋ごと実施し、その後、2〜8cm程度の厚さで、通気性ある板上に広げ、熱風の向きが上下変化する乾燥室内に入れ、例えば、第1乾燥室では50℃、第2乾燥室では70℃、第3及び第4乾燥室では85℃というように順次温度を変化させて、十分乾燥するのがよい。
この乾燥工程で、繊維に対する架橋結合が確実となり、弾力性が高められ、また、繊維への柔軟性付与も達成できる。
For the drying process after dehydration, cellulosic filaments can be used with ordinary tunnel dryers, but for viscose table fiber, the oil-treated and dehydrated products are placed in a breathable bag and the whole bag is used. Then, spread it on a breathable plate with a thickness of about 2 to 8 cm, and put it in a drying chamber where the direction of hot air changes up and down, for example, 50 ° C. in the first drying chamber, 70 ° C. in the second drying chamber, In the third and fourth drying chambers, it is preferable that the temperature is sequentially changed to 85 ° C. to sufficiently dry.
In this drying step, the cross-linking to the fiber is ensured, the elasticity is increased, and the fiber can be imparted with flexibility.

本発明の油剤は、ジメチロール尿素をそのまま使用しないで、アセチックジメチロール尿素として使用するので、環境に優しく、しかも、特別な触媒を使用しなくても、非常に効率よく、安定してセルロース系繊維に架橋結合を生じさせることができる。本発明の油剤で処理したセルロース系繊維は、従来になく、弾力性に優れるものであり、また、染色性にも優れたものとなある。 Since the oil agent of the present invention is used as acetic dimethylol urea without using dimethylol urea as it is, it is environmentally friendly, and it is very efficient and stable without using a special catalyst. Crosslinks can be created in the fibers. Cellulosic fibers treated with the oil agent of the present invention are unprecedented and are excellent in elasticity and dyeability.

以下、ビスコースステープルファイバーに本発明油剤を使用する例と、セルロース系フィラメントに本発明の油剤を使用する例について、説明する。
A.ビスコースステープルファイバーに本発明油剤を使用する場合:
この例では、環境に優しく人体に害のないビスコースステープルファイバーを、本発明の油剤で処理することにより、弾力性及び柔軟性を恒久的に保有する製品とする。
その方法は下記の通りである。
a.必要な長さに切断したビスコースステープルファイバーを本発明油剤で浸漬処理する。
b.aで処理したファイバーを、脱水して、トンネル乾燥機に送る。
c.トンネル乾燥機で乾燥させる。
Hereafter, the example which uses this invention oil for a viscose staple fiber, and the example which uses the oil of this invention for a cellulose filament are demonstrated.
A. When using the oil of the present invention for viscose staple fiber:
In this example, a viscose staple fiber that is environmentally friendly and harmless to the human body is treated with the oil of the present invention to obtain a product that permanently retains elasticity and flexibility.
The method is as follows.
a. A viscose staple fiber cut to a required length is dipped with the oil of the present invention.
b. The fiber treated with a is dehydrated and sent to the tunnel dryer.
c. Dry with a tunnel dryer.

[aの工程]
ビスコースステープルファイバーを一定量ずつ、ポリエステル製布帛からなるジップ付きの袋に入れ、この袋を、本発明の油剤(pH6.5〜6.8の酸性水中にポリオキシエチレンエーテル型の界面活性剤とアルキルポリアミン誘導体の陽イオン界面活性剤との1:1.25混合液を0.25〜0.3重量%、アセチックジメチロール尿素0.012重量%を含有する)を約45℃の温度を保持しながら、循環させている浸漬浴に約20分間浸漬し、アセチックジメチロール尿素を、ファイバーに、浸透させ、セルロース分子にアセチックジメチロール尿素による架橋結合を十分生じるようにする
[Step a]
A certain amount of viscose staple fiber is put into a bag with a zip which is made of a polyester fabric, and the bag is placed in the oil agent of the present invention (polyoxyethylene ether type surfactant in acidic water of pH 6.5 to 6.8). And a cationic surfactant of alkylpolyamine derivative containing 0.25 to 0.3% by weight of a mixture of 1: 1.25 and 0.012% by weight of acetic dimethylolurea) at a temperature of about 45 ° C. So that the acetylene dimethylolurea penetrates into the fiber so that the cellulose molecules are sufficiently cross-linked by the acetodimethylolurea.

[bの工程]
aの浸漬浴で油剤処理した袋入りのフィラメントを袋のまま遠心分離脱水機に入れて、必要量の脱水をする。その後、袋のジッパーを開き、ビスコースステープルファイバーを取出し、よくかき混ぜ、次いで、別に乾燥したポリエステル製布帛からなる袋のジッパーを開き、その中にステンレス枠(高さ約6cm)を入れ、袋の中のステンレス枠内に脱水したビスコースステープルファイバーを均一に広げて、ジッパーを閉じ、この袋を、カートの棚に載置する。
このカートは、上下3段の通気性ある棚を有し、全体に24個の袋を載置することができるようになっている。袋の大きさは、長さ約88cm、幅約88cm、高さ約6cmとした。
[Step b]
The filament in the bag treated with the oil agent in the immersion bath of a is put in a centrifugal dehydrator as it is and dehydrated as much as necessary. After that, open the zipper of the bag, take out the viscose staple fiber, stir well, then open the zipper of the bag made of polyester fabric separately dried, put a stainless frame (height about 6cm) in it, The dehydrated viscose staple fiber is spread evenly in the stainless steel frame inside, the zipper is closed, and the bag is placed on the cart shelf.
This cart has three upper and lower air-permeable shelves and can carry 24 bags in total. The size of the bag was about 88 cm in length, about 88 cm in width, and about 6 cm in height.

[cの工程]
カートは5個の乾燥室A,B,C,D,Eからなるトンネル式乾燥機に送られる。
乾燥機の中央にはレールが設けられており、このレール上をカートが乾燥室AからEに順次送られるようになっている。
乾燥室Aは55℃、乾燥室Bは70℃、乾燥室C及びDは85℃、乾燥室Eは放冷室となっており、新鮮な空気の入口の流入調整で温度を下げて乾燥室Eからカートを取出すようになっている。
カート上のビスコースステープルファイバーは、カートと共に乾燥機内を移動し、5個の乾燥室の中で40分ずつ40分×5=200分間乾燥した後、乾燥室Eから外部に取出され、その後、新たなカートが、乾燥室Aに導入され、上記乾燥工程が再開されるのである。
かかる乾燥工程により、本発明の油剤をビスコースステープルファイバーに均一に作用させ、ビスコースステープルファイバーにおける架橋結合を確かなものとすることができ、ビスコースステープルファイバーに弾力性と柔軟性を恒久的に付与できるのである。
[Step c]
The cart is sent to a tunnel dryer consisting of five drying chambers A, B, C, D and E.
A rail is provided in the center of the dryer, and the cart is sequentially sent from the drying chambers A to E on the rail.
The drying chamber A is 55 ° C., the drying chamber B is 70 ° C., the drying chambers C and D are 85 ° C., the drying chamber E is a cooling chamber, and the temperature is lowered by adjusting the inflow of fresh air at the drying chamber. The cart is taken out from E.
The viscose staple fiber on the cart moves in the dryer together with the cart, is dried for 40 minutes × 5 = 200 minutes in 5 drying chambers, and is then taken out from the drying chamber E. A new cart is introduced into the drying chamber A, and the drying process is resumed.
By this drying step, the oil agent of the present invention can be applied uniformly to the viscose staple fiber to ensure the cross-linking in the viscose staple fiber, and the viscose staple fiber is permanently elastic and flexible. It can be given to.

各乾燥室は電気ヒーターによる熱風ファンにより乾燥するようになっているが、乾燥室Aは上方左側から熱風が下方に送られ、右側で下方から上方に熱風が送られ、右側上部のダクトを通り排気ファンにより排気されるようになっており、乾燥室Bは上方右側から熱風が下方に送られ、左側で下方から上方に熱風が送られ、左上部のダクトを通り排気ファンにより排気されるようになっており、乾燥室Cは左側上方から熱風が下方に送られ、右側で下方から上方に熱風が送られ、右側上部のダクトを通り排気ファンにより排気され、更に乾燥室Dは上方右側から熱風が下方に向けて送られ、左側で下方から上方に熱風が送られ、上部のドアの窓の開閉で、調整されながら排気され、その後、乾燥室Eではカートが冷却されるようになっていす。全熱風ファンを停止し、乾燥室A及びEのドアを開き、約60℃以下に冷却されたカートを、取出すと同時に、再び、新しいカートを乾燥室Aに入れ、乾燥室Aから乾燥機Eまで順次移動させ、乾燥を繰り返せばよい。 Each drying chamber is dried by a hot air fan using an electric heater. In the drying chamber A, hot air is sent downward from the upper left side, and hot air is sent from the lower side to the upper side on the right side. In the drying chamber B, hot air is sent downward from the upper right side, hot air is sent from the lower side to the upper side on the left side, and exhausted by the exhaust fan through the upper left duct. In the drying chamber C, hot air is sent downward from the upper left side, hot air is sent from the lower side to the upper side on the right side, exhausted by the exhaust fan through the duct on the upper right side, and the drying chamber D is further opened from the upper right side. Hot air is sent downward, hot air is sent from the lower side to the upper side on the left side, and exhausted while being adjusted by opening and closing the upper door window, and then the drying room E cools the cart. YouThe hot air fan is stopped, the doors of the drying chambers A and E are opened, and the cart cooled to about 60 ° C. or less is taken out. At the same time, a new cart is again put into the drying chamber A. It is sufficient to move to 1 and repeat drying.

このようにして、本発明の油剤で処理したビスコースステープルファイバーは、紡績糸単独であっても混紡糸としても、非常に優秀な弾力性を有するものとなる。また、製織製編効率が良く、染色性も非常に優れ、鮮明な染色品を得ることができる。 In this way, the viscose staple fiber treated with the oil of the present invention has very excellent elasticity, whether it is a single spun yarn or a blended yarn. In addition, weaving and knitting efficiency is good, dyeability is very excellent, and a clear dyed product can be obtained.

更に、本発明の製品は、弾力性に優れるため、肉眼的にも、従来の製品に比してボリューム感あるものとなる。 Furthermore, since the product of the present invention is excellent in elasticity, it has a sense of volume as compared with the conventional product.

B.セルロース系フィラメントに本発明の油剤を使用する場合
ビスコースレーヨンフィラメントを紡糸後、本発明の油剤(Aと同様のもの)を使用して油剤処理する。
本発明の油剤の活動は、ポリオキシエチレンエーテル型の界面活性剤(この例では、松本油脂製薬製のActinol-R-100)の強力な浸透作用により、繊維の非結晶部分に油剤は均一に浸透分散されて、特にアセチックジメチロール尿素が架橋結合を始め、繊維の非結晶部分に、自然に多数の架橋結合を生じる。
B. When the oil agent of the present invention is used for the cellulosic filament, the viscose rayon filament is spun and then treated with the oil agent of the present invention (the same as A).
The activity of the oil agent of the present invention is due to the strong osmotic action of a polyoxyethylene ether type surfactant (in this example, Actinol-R-100 manufactured by Matsumoto Yushi Seiyaku Co., Ltd.), and the oil agent is uniformly distributed in the non-crystalline portion of the fiber. Osmotically dispersed, especially acetyl dimethylol urea begins to crosslink and naturally produces a large number of crosslinks in the non-crystalline portion of the fiber.

Figure 2006214039
Figure 2006214039

脱水後、通常のトンネル乾燥機で温度上昇と共に架橋結合が起こり、容積の縮小で非結晶部分に侵入されているアルキルポリアミン誘導体の陽イオン界面活性剤(この例では、松本油脂製薬製のZONTES-TA-460-15)の柔軟平滑剤が繊維の表面に付着し、その平滑性のため、フィラメントの分離がたやすく出来、水分蒸発路が開かれ、密に巻かれたフィラメントの分離がし易くなり、表面の平滑性とアセチックジメチロール尿素の架橋結合による分子の配列が若干の張力によっても、分子の配列が同一方向に向けられ弾力性の分子配列が起こり(同一方向に)、延伸状態で固く巻かれたフィラメント内外の繊度が均一化され、製織製編能率向上と鮮明な染色並びに柔軟弾力性ある製品製造が可能となり、新製品ができるようになった。 After dehydration, a cationic tunneling agent of an alkylpolyamine derivative that crosslinks with an increase in temperature in a normal tunnel dryer and invades into the amorphous part due to a reduction in volume (in this example, ZONTES- TA-460-15) soft smoothing agent adheres to the surface of the fiber, and due to its smoothness, the filament can be easily separated, the water evaporation path is opened, and the densely wound filament is easily separated. Even if the molecular alignment due to the smoothness of the surface and the cross-linking of acetyldimethylolurea causes a slight tension, the molecular alignment is directed in the same direction, causing an elastic molecular alignment (in the same direction), and the stretched state. The fineness inside and outside of the filament wound tightly is made uniform, which improves the weaving and knitting efficiency, makes it possible to produce clear and flexible products, and makes new products possible.

Claims (5)

酸性水中に、ポリオキシエチレンエーテル型の界面活性剤とアルキルポリアミン誘導体の陽イオン界面活性剤との混合液と、アセチックジメチロール尿素を重量比率で0.6〜50:1の割合で含有することを特徴とするセルロース系繊維用油剤。 A mixture of a polyoxyethylene ether type surfactant and an alkyl polyamine derivative cationic surfactant and an acetic dimethylolurea are contained in acidic water in a weight ratio of 0.6 to 50: 1. An oil for cellulosic fibers characterized by the above. 前記ポリオキシエチレンエーテル型の界面活性剤とアルキルポリアミン誘導体の陽イオン界面活性剤との混合液0.1〜0.4重量%と、アセチックジメチロール尿素0.008〜0.018重量%を含有することを特徴とする請求項1の油剤。 0.1 to 0.4% by weight of a mixture of the polyoxyethylene ether type surfactant and an alkyl polyamine derivative cationic surfactant and 0.008 to 0.018% by weight of acetyldimethylolurea It contains, The oil agent of Claim 1 characterized by the above-mentioned. 上記ポリオキシエチレンアルキルエーテル型の界面活性剤とアルキルポリアミン誘導体の陽イオン界面活性剤との混合重量比率が1:1〜1:5である請求項1又は2の油剤。 The oil agent according to claim 1 or 2, wherein a mixing weight ratio of the polyoxyethylene alkyl ether type surfactant and the alkyl polyamine derivative cationic surfactant is 1: 1 to 1: 5. 上記アセチックジメチロール尿素が低縮合物のジメチロール尿素と酢酸の化合物である請求項1〜3いずれか1項の油剤。 The oil agent according to any one of claims 1 to 3, wherein the acetyl dimethylol urea is a compound of dimethylol urea and acetic acid as a low condensate. セルロース系繊維製品を、ポリオキシアルキルエーテル界面活性剤とアルキルポリアミン誘導体の陽イオン界面活性剤との混合液0.1〜0.4重量%とアセチックジメチロール尿素0.008〜0.018重量%を含有する酸性の水性油剤に浸漬処理し、脱水後、80℃以上で乾燥することを特徴とする弾力性と柔軟性を耐久性よく保持するセルロース系繊維製品の製造方法。 Cellulosic fiber products were prepared by mixing 0.1 to 0.4% by weight of a mixed solution of a polyoxyalkyl ether surfactant and an alkyl polyamine derivative cationic surfactant and 0.008 to 0.018% by weight of acetic dimethylol urea. A method for producing a cellulosic fiber product that retains elasticity and flexibility in a durable manner, characterized in that it is immersed in an acidic aqueous oil containing 100%, dehydrated and dried at 80 ° C. or higher.
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Publication number Priority date Publication date Assignee Title
CN112301745A (en) * 2020-11-20 2021-02-02 沈阳浩博实业有限公司 Oil agent for continuous spunbond fibers and preparation method and application thereof

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112301745A (en) * 2020-11-20 2021-02-02 沈阳浩博实业有限公司 Oil agent for continuous spunbond fibers and preparation method and application thereof
CN112301745B (en) * 2020-11-20 2023-12-01 沈阳浩博实业有限公司 Oiling agent for continuous spinning viscose fiber and preparation method and application thereof

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