JPS6143469B2 - - Google Patents
Info
- Publication number
- JPS6143469B2 JPS6143469B2 JP57215873A JP21587382A JPS6143469B2 JP S6143469 B2 JPS6143469 B2 JP S6143469B2 JP 57215873 A JP57215873 A JP 57215873A JP 21587382 A JP21587382 A JP 21587382A JP S6143469 B2 JPS6143469 B2 JP S6143469B2
- Authority
- JP
- Japan
- Prior art keywords
- melamine
- weight
- salts
- synthetic fibers
- processing method
- 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
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
本発明は、メラミン誘導体を用いた合成繊維の
防融加工方法に関するものである。
合成繊維に共通した欠点の1つとして煙草の
火、火粉等の接触により容易に穴があいたり変質
して、その商品価値を損うだけでなく人体への危
険性も大きい事が挙げられる。このような観点か
ら合成繊維に防融性を付与してほしいという要望
が多方面から挙がつている。
従来合成繊維の防融加工に関してはメラミン誘
導体と無機酸、有機酸、又はその塩との混合水溶
液を付着せしめた後水分の存在下に加熱処理する
特公昭48−12479号公報記載の方法、又はその混
合水溶液中にアニオン界面活性剤を添加する特公
昭49−32760号公報記載の方法等が知られてい
る。これらの方法により得られる繊維は防融性を
有するものの、加工液の安定性に欠けたり、加工
布の色相の変化いわゆる白化現象が生じたりする
欠点が認められる。また、無触媒でメラミン誘導
体を含む水溶液で加熱処理する特開昭54−93198
号公報記載の方法等も知られているが、この方法
では白化現象は緩和されるものの、加工に高圧装
置を要したり、長時間を要するなど作業性が悪
く、しかも付与量が少ないと防融効果の耐洗濯性
が悪くなるという欠点を有する。
本発明者等は鋭意研究の結果、かかる欠点のな
い合成繊維の防融加工方法を完成したものであ
る。
本発明の目的は所謂白化現象を伴うことなく、
耐洗濯性ある優れた防融性を有する合成繊維を、
工業的に容易且つ安価な方法で製造する加工方法
を提供するにある。
本発明の方法は合成繊維にアンモニア水、塩化
アンモニウム、メラミン誘導体、及びポリアクリ
ル酸、ポリメタクリル酸及びそれらの塩類からな
る群から選ばれる少なくとも1種の親水性重合体
を含む処理液を付着せしめた後、湿熱処理するこ
とを特徴とする。
本発明に適用する合成繊維としては、ポリエス
テル繊維、ポリアミド繊維、アクリル繊維、ポリ
オレフイン系繊維等があり、これらは綿、糸、織
編物、不織布等、任意の形状で用いることが出来
る。これらの合成繊維は相互に又は天然繊維など
の非熱溶融性繊維と混紡、交織、或は交編して使
用することも出来る。
本発明に適用するアンモニア水は通常用いられ
ている25%(重量パーセント)前後の濃度のもの
で十分である。
本発明に適用するポリアクリル酸及びポリメタ
クリル酸の塩類は水溶性の塩でありアルカリ金属
塩、アンモニウム塩であるのが好ましい。親水性
重合体としては線状のものばかりでなく架橋分岐
型のものも使用できる。また、ポリアクリル酸等
の重合度については、例えば固形分40%のもので
粘度が20000cps以下、好ましくは2000cps以下の
ものが使い易いが、これに限定するものではな
い。
本発明に適用するメラミン誘導体としては、通
常知られているメラミン誘導体、例えばヘキサメ
チロールメラミン、ペンタメチロールメラミン、
トリ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、ジメチ
ロールメラミン、ビスメトキシメチロールメラミ
ンなどのメチロール誘導体が挙げられる。これら
の中でヘキサメチロールメラミン、ペンタメチロ
ールメラミン、トリメチロールメラミンの使用が
特に好ましい。
本発明の方法に於いて、アンモニア水、塩化ア
ンモニウム、メラミン誘導体及び親水性重合体は
通常水溶液として合成繊維に付与せしめる。処理
液中のメラミン誘導体の濃度は目的とする繊維の
風合又は加工条件、或いは親水性重合体の種類、
濃度等により異なるが通常3〜20重量%、好まし
くは5〜15重量%である。親水性重合体の濃度も
上述の条件等により異なるが通常0.1〜10重量%
で、0.5〜5重量%が好適である。塩化アンモニ
ウムは通常0.1〜5重量%程度使用する。アンモ
ニア水は通常25%濃度の水溶液で0.15〜7.5重量
%程度使用するが、塩化アンモニウムと25%アン
モニア水の比率が1:1.5で使用するのが液の安
定性を助長するため好ましい。処理液中のメラミ
ン誘導体化合物100重量部に対して親水性重合体
は通常5〜40重量部、好ましくは10〜35重量部の
割合で使用する。又水溶液は常温で使用するのが
操業上もつとも容易である。
本発明の処理液はパツド法、浸漬法、噴霧法、
塗布法等適宜の手段で合成繊維に付与することが
出来る。
処理液を付与した合成繊維には、次いで乾燥す
ることなく湿熱処理を施す。湿熱処理は通常蒸熱
で行う。湿熱処理は通常、温度60〜180℃、好ま
しくは95〜160℃であり、処理時間は処理温度に
よつて異なるが通常3〜180分、好ましくは5〜
60分である。
次いで常法に従つて、ソーピング、水洗、乾
燥、仕上セツト等を行つて最終製品とするが、必
要あれば仕上セツト時に弗素系樹脂による撥水撥
油加工、シリコン系樹脂等による撥水加工、その
他帯電防止加工等の加工剤処理を行つてもよい。
本発明の方法によれば色相のくすみが生ずるこ
となく、耐洗濯性のあるすぐれた防融性をもつ合
成繊維製品を容易に得ることが可能であり、また
加工による風合の硬化もなく、製品を柔軟に仕上
げることができる。本発明の方法では、ポリアク
リル酸等の親水性重合体がメラミン誘導体と架橋
し、白化防止や風合の改良、防融性の耐洗濯性の
向上などに寄与するものと思われる。
次に本発明の実施例を示す。実施例に示す試験
結果は次の方法に基くものである。
処理液の安定性
30℃で所定時間放置し、調製時と同じ状態を保
つているものを〇印、白濁や沈澱を×印とする。
樹脂付着率
未処理布に対する処理布の重量増加率を%で示
す。
色相変化
分光光度計で測定した処理布と未処理布の色差
△Eで示す。
防融性
(1) ガラス球試験
重量1.5g、直径1.5cmのガラス中空球を直径
3cmのルツボに入れ、電気炉で加熱する。所定
の温度に加熱された時ルツボごと取り出して布
の上にガラス球を落す。ガラス中空球が布を溶
融して、下に落下するに必要な最低加熱温度を
示す。
(2) 煙草接触試験
火のついた煙草を自重で布に垂直に立て、30
秒間接触後の状態を観察する。数字は溶融孔の
大きさ(径)を示す。( )内の数字は焦跡の
大きさ(径)を示す。
防融性試験はいずれも、耐洗濯性を試験するた
め、加工上り(未洗濯)のものと下記の条件で連
続10回洗濯した後のものについて実施した。
洗濯機:日立PF2000青空で標準サイクル(洗浄
12分、その他13分計25分)
洗濯試料重量:720g
洗剤:36g
水量:36
温度:40℃
実施例 1
常法によつて分散染料で紺に染色したポリエス
テルギヤバジン(目付218g/m2)に第1表で示し
た組成の処理液を100重量%になる様にパツド
し、乾燥さすことなく相対湿度98%、温度102℃
の蒸気中で10分間蒸熱処理を行い、しかるのち、
非イオン界面活性剤2g/を用い、80℃で10分
間ソーピング処理をし、乾燥した。処理布につい
て樹脂付着率、色差△E及び防融性(洗濯前と10
回連続洗濯後)を測定した。その結果を第2表に
示す。また処理液について調製後24時間及び48時
間後の安定性を観察した結果を第1表に示す。
The present invention relates to a method for melt-proofing synthetic fibers using melamine derivatives. One of the common drawbacks of synthetic fibers is that they are easily perforated or deteriorated by contact with cigarette smoke, spark powder, etc., which not only reduces their commercial value but also poses a great danger to the human body. . From this point of view, there have been requests from various quarters for synthetic fibers to have melt-proofing properties. Conventional methods for melt-proofing synthetic fibers include the method described in Japanese Patent Publication No. 12479/1983, in which a mixed aqueous solution of a melamine derivative and an inorganic acid, an organic acid, or a salt thereof is applied and then heat-treated in the presence of moisture; A method described in Japanese Patent Publication No. 49-32760, in which an anionic surfactant is added to the mixed aqueous solution, is known. Although the fibers obtained by these methods have melt-proofing properties, they have disadvantages such as a lack of stability of the processing liquid and a change in the hue of the processed fabric, so-called whitening phenomenon. In addition, JP-A No. 54-93198 heat-treated with an aqueous solution containing a melamine derivative without a catalyst.
The method described in the above publication is also known, but although this method alleviates the whitening phenomenon, it requires high-pressure equipment for processing, takes a long time, and has poor workability.Moreover, if the amount applied is small, it is difficult to prevent the problem. It has the disadvantage of poor washing resistance due to the melting effect. As a result of intensive research, the present inventors have completed a method for melt-proofing synthetic fibers that does not have these drawbacks. The purpose of the present invention is to eliminate the so-called whitening phenomenon,
Synthetic fibers with excellent wash resistance and melt resistance,
It is an object of the present invention to provide a processing method that is industrially easy and inexpensive. In the method of the present invention, a treatment liquid containing aqueous ammonia, ammonium chloride, melamine derivatives, and at least one hydrophilic polymer selected from the group consisting of polyacrylic acid, polymethacrylic acid, and salts thereof is applied to synthetic fibers. After that, it is characterized by being subjected to moist heat treatment. Synthetic fibers applicable to the present invention include polyester fibers, polyamide fibers, acrylic fibers, polyolefin fibers, and the like, and these can be used in any form such as cotton, yarn, woven or knitted fabrics, or nonwoven fabrics. These synthetic fibers can also be used by blending, interweaving, or interweaving with each other or with non-thermofusible fibers such as natural fibers. The ammonia water used in the present invention has a concentration of about 25% (weight percent), which is commonly used, and is sufficient. The salts of polyacrylic acid and polymethacrylic acid applied to the present invention are water-soluble salts, and are preferably alkali metal salts or ammonium salts. As the hydrophilic polymer, not only linear polymers but also crosslinked and branched polymers can be used. Regarding the degree of polymerization of polyacrylic acid, for example, one having a solid content of 40% and a viscosity of 20,000 cps or less, preferably 2,000 cps or less is easy to use, but it is not limited to this. The melamine derivatives applicable to the present invention include commonly known melamine derivatives, such as hexamethylolmelamine, pentamethylolmelamine,
Examples include methylol derivatives such as trimethylolmelamine, hexakismethoxymethylolmelamine, trismethoxymethylolmelamine, trismethoxymethylmelamine, dimethylolmelamine, and bismethoxymethylolmelamine. Among these, it is particularly preferable to use hexamethylolmelamine, pentamethylolmelamine, and trimethylolmelamine. In the method of the present invention, aqueous ammonia, ammonium chloride, melamine derivatives and hydrophilic polymers are usually applied to synthetic fibers as aqueous solutions. The concentration of the melamine derivative in the treatment solution depends on the texture of the target fiber or processing conditions, the type of hydrophilic polymer,
Although it varies depending on the concentration etc., it is usually 3 to 20% by weight, preferably 5 to 15% by weight. The concentration of the hydrophilic polymer also varies depending on the conditions mentioned above, but it is usually 0.1 to 10% by weight.
0.5 to 5% by weight is suitable. Ammonium chloride is usually used in an amount of about 0.1 to 5% by weight. Aqueous ammonia is usually used in an aqueous solution with a concentration of 25% and is used in an amount of about 0.15 to 7.5% by weight, but it is preferable to use the ratio of ammonium chloride to 25% ammonia water in a ratio of 1:1.5 in order to promote stability of the solution. The hydrophilic polymer is usually used in an amount of 5 to 40 parts by weight, preferably 10 to 35 parts by weight, per 100 parts by weight of the melamine derivative compound in the treatment liquid. In addition, it is easy to use the aqueous solution at room temperature. The treatment liquid of the present invention can be applied by the pad method, dipping method, spray method,
It can be applied to synthetic fibers by any suitable means such as a coating method. The synthetic fibers to which the treatment liquid has been applied are then subjected to a moist heat treatment without drying. Moist heat treatment is usually performed using steam heat. The moist heat treatment is usually performed at a temperature of 60 to 180°C, preferably 95 to 160°C, and the treatment time varies depending on the treatment temperature, but is usually 3 to 180 minutes, preferably 5 to 160°C.
It is 60 minutes. Next, soaping, washing with water, drying, finishing setting, etc. are performed in accordance with conventional methods to obtain the final product. If necessary, water and oil repellent treatment with fluorine resin, water repellent treatment with silicone resin, etc. is applied during finishing setting. Other processing agents such as antistatic processing may also be performed. According to the method of the present invention, it is possible to easily obtain synthetic fiber products with excellent wash resistance and melt resistance without dulling of hue, and without hardening of texture due to processing. Products can be finished flexibly. In the method of the present invention, a hydrophilic polymer such as polyacrylic acid is crosslinked with a melamine derivative, which is thought to contribute to prevention of whitening, improvement of texture, and improvement of melt resistance and washing resistance. Next, examples of the present invention will be shown. The test results shown in the Examples are based on the following method. Stability of the treatment solution After being left at 30℃ for a specified period of time, those that remain in the same state as when prepared are marked with an ○, and those that are cloudy or precipitated are marked with an x. Resin adhesion rate The weight increase rate of treated fabric relative to untreated fabric is shown in %. Hue change Shown as the color difference ΔE between treated and untreated fabrics measured with a spectrophotometer. Melting Resistance (1) Glass Ball Test A glass hollow sphere weighing 1.5 g and having a diameter of 1.5 cm is placed in a crucible with a diameter of 3 cm and heated in an electric furnace. When the crucible has been heated to a predetermined temperature, the whole crucible is taken out and the glass bulb is dropped onto a cloth. Indicates the minimum heating temperature required for the glass hollow sphere to melt the cloth and fall to the bottom. (2) Cigarette contact test A lighted cigarette was held vertically against a cloth under its own weight, and then held for 30 minutes.
Observe the condition after contact for a second. The numbers indicate the size (diameter) of the melt pores. The numbers in parentheses indicate the size (diameter) of the focus. In order to test the washing resistance, the melt resistance test was carried out on the processed (unwashed) products and the products that had been washed 10 times in a row under the following conditions. Washing machine: Hitachi PF2000 blue sky standard cycle (washing)
12 minutes, other 13 minutes, total 25 minutes) Washing sample weight: 720g Detergent: 36g Water amount: 36 Temperature: 40°C Example 1 Polyester gear bagine dyed navy blue with disperse dye by conventional method (fabric weight 218g/m 2 ) 100% by weight of the treatment solution shown in Table 1, and heated to 98% relative humidity and 102°C without drying.
Steam treatment for 10 minutes in the steam of
A soaping treatment was performed at 80° C. for 10 minutes using 2 g of a nonionic surfactant, followed by drying. Resin adhesion rate, color difference △E and melt resistance (before washing and 10
(after continuous washing) was measured. The results are shown in Table 2. Table 1 also shows the results of observing the stability of the treatment solution 24 hours and 48 hours after preparation.
【表】【table】
【表】【table】
【表】
第1表及び第2表の結果に見る如く、本発明の
方法では処理液の安定性が非常にすぐれており、
30℃で48時間以上安定であるため、操業がやり易
く、また製品は色差△Eも小さく白化の程度が非
常に少なく、しかも耐久性ある優れた防融性を有
するため、非常に商品価値あるものとなる。
実施例 2
ナイロン編物(目付340g/m2)に実施例1No.2
の処理液を100重量%施与し相対湿度100%、100
℃で10分熱処理を行ない、ソーピングして未反応
の化合物を洗浄除去し、乾燥した。処理布は色調
のくすみがなく、煙草接触テストで開孔を見ず、
焦跡も小さかつた。これに対し未処理布は5秒の
接触で3mmの開孔が、10秒の接触で7mmの開孔が
見られた。[Table] As can be seen from the results in Tables 1 and 2, the stability of the treatment liquid in the method of the present invention is extremely excellent.
It is stable for more than 48 hours at 30℃, making it easy to operate, and the product has a small color difference △E and very little whitening. Moreover, it has excellent durability and melt resistance, making it extremely valuable as a commercial product. Become something. Example 2 Example 1 No. 2 on nylon knitted fabric (basis weight 340g/m 2 )
Apply 100% by weight of the treatment solution at a relative humidity of 100% and 100% by weight.
Heat treatment was performed at ℃ for 10 minutes, unreacted compounds were washed off by soaping, and the mixture was dried. The treated cloth has no dull color and no holes were observed in the cigarette contact test.
The scar was also small. On the other hand, in the untreated cloth, 3 mm pores were observed after 5 seconds of contact, and 7 mm pores were observed after 10 seconds of contact.
Claims (1)
ウム、(c)メラミン誘導体、並びに(d)ポリアクリル
酸、ポリメタクリル酸及びそれらの塩類からなる
群から選ばれる少なくとも1種の親水性重合体を
含む処理液を付着せしめた後、湿熱処理すること
を特徴とする合成繊維の防融加工方法。 2 メラミン誘導体がメラミンのメチロール誘導
体である特許請求の範囲第1項記載の加工方法。 3 メラミンのメチロール誘導体がヘキサメチロ
ールメラミン、ペンタメチロールメラミン又はト
リメチロールメラミンである特許請求の範囲第2
項記載の加工方法。 4 ポリアクリル酸及びポリメタクリル酸の塩類
がアルカリ金属塩又はアンモニウム塩である特許
請求の範囲第1項〜第3項いずれか1項に記載の
加工方法。 5 処理液がメラミン誘導体100重量部に対し
て、親水性重合体5〜40重量部を含む特許請求の
範囲第1項〜第4項いずれか1項に記載の加工方
法。[Claims] 1 Synthetic fibers containing at least one selected from the group consisting of (a) aqueous ammonia, (b) ammonium chloride, (c) melamine derivatives, and (d) polyacrylic acid, polymethacrylic acid, and salts thereof. A method for melt-proofing synthetic fibers, which comprises applying a treatment liquid containing one kind of hydrophilic polymer and then subjecting the fibers to a moist heat treatment. 2. The processing method according to claim 1, wherein the melamine derivative is a methylol derivative of melamine. 3. Claim 2 in which the methylol derivative of melamine is hexamethylolmelamine, pentamethylolmelamine or trimethylolmelamine.
Processing method described in section. 4. The processing method according to any one of claims 1 to 3, wherein the salts of polyacrylic acid and polymethacrylic acid are alkali metal salts or ammonium salts. 5. The processing method according to any one of claims 1 to 4, wherein the treatment liquid contains 5 to 40 parts by weight of the hydrophilic polymer based on 100 parts by weight of the melamine derivative.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21587382A JPS59106580A (en) | 1982-12-07 | 1982-12-07 | Melt-proof processing of synthetic fiber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21587382A JPS59106580A (en) | 1982-12-07 | 1982-12-07 | Melt-proof processing of synthetic fiber |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59106580A JPS59106580A (en) | 1984-06-20 |
| JPS6143469B2 true JPS6143469B2 (en) | 1986-09-27 |
Family
ID=16679671
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP21587382A Granted JPS59106580A (en) | 1982-12-07 | 1982-12-07 | Melt-proof processing of synthetic fiber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59106580A (en) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5135793A (en) * | 1974-09-17 | 1976-03-26 | Mitsubishi Rayon Co | GOSEISENINOSHINSUIKAKAGOHO |
-
1982
- 1982-12-07 JP JP21587382A patent/JPS59106580A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59106580A (en) | 1984-06-20 |
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