JPS6143468B2 - - Google Patents
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- Publication number
- JPS6143468B2 JPS6143468B2 JP57215872A JP21587282A JPS6143468B2 JP S6143468 B2 JPS6143468 B2 JP S6143468B2 JP 57215872 A JP57215872 A JP 57215872A JP 21587282 A JP21587282 A JP 21587282A JP S6143468 B2 JPS6143468 B2 JP S6143468B2
- Authority
- JP
- Japan
- Prior art keywords
- melamine
- salts
- melt
- processing method
- weight
- 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
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Description
本発明はメラミン誘導体を使用した合成繊維の
防融加工法の改良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。
更にメラミン誘導体、酸性触媒、並びにアニオン
界面活性剤の混合水溶液を付着させ、水分の蒸散
を防止した状態で室温に放置する特公昭53−
19719号公報記載の方法等も知られているが、こ
れらの方法により得られる繊維は防融性を有する
ものの加工布の色相の変化いわゆる白化現象が生
じる欠点を有している。また、無触媒でメラミン
誘導体を含む水溶液を付与し、加熱処理する特開
昭54−93198号公報記載の方法、及び無触媒で水
溶性高分子化合物とメラミン誘導体を含む水溶液
を付着させ加熱処理する特開昭54−106692号公報
記載の方法も知られるが、これらの方法では白化
現象は緩和されるものの、付着性及び再現性に欠
け、高圧装置を必要とし、しかも十分な付着量を
得られないことから防融効果の耐洗濯性が悪くな
るという欠点があつた。
そこで、我々は、これらの欠点を改良し、所謂
白化現象のない、色調の鮮明性を有し、しかも耐
洗濯性を有する合成繊維の防融加工法を提供する
べく鋭意研究し、その結果、先に特願昭56−
123474号の特許出願をしたが、この方法はメラミ
ン誘導体とポリアクリル酸の塩と無機酸塩触媒を
併含する処理液を使用し、湿熱処理を必要とする
ものであつた。
この方法によつて、所望の効果は得られたが、
我々は更に安価に効率よく所望の効果を得ること
ができないかと研究を続け、本発明を達成したも
のである。
本発明の目的は、無機酸塩触媒や湿熱処理を必
要とすることなく、工業的に非常に容易かつ安価
な方法で、合成繊維に所謂白化現象を伴うことな
く、耐洗濯性ある防融性及び吸水性を付与できる
方法を提供することにある。
本発明の方法は、合成繊維にメラミン誘導体
と、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水性処理液を付着させた
後、水分の蒸散を防止した状態で室温に放置する
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。また、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、ビスメトキシメチルメチロール
メラミン等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。
本発明に用い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。ポリア
クリル酸等は線状の重合体だけでなく架橋分岐型
のものでもよい。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。
本発明の方法では、メラミン誘導体化合物と親
水性重合体を水性処理液、主に水溶液として合成
繊維に付与せしめる。この処理液中のメラミン誘
導体化合物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%が好ましい。処理液中のメラミン
誘導体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。この範囲で用いると白化防止の効果、防
融性の洗濯耐久性向上の効果が著しい。なお、処
理液は常温で使用するのが操業上もつとも容易で
ある。
本発明の処理液には界面活性剤を添加してもよ
く、界面活性剤としてはアニオン界面活性剤が好
ましい。アニオン界面活性剤はメラミン誘導体及
び親水性重合体により形成される皮膜の形成を助
長するものであり、浸透性を助長するために非イ
オン界面活性剤を併用してもよい。アニオン界面
活性剤には次のものが含まれる。例えば、石ケ
ン、ザルコシネートのカルボン酸系アニオン活性
剤、高級アルコール硫酸エステル塩、硫酸化油、
硫酸化脂肪酸エステル、硫酸化オレフイン、等の
硫酸エステル塩系のアニオン活性剤、アルキルベ
ンゼンスルホン酸塩、アルキルナフタリンスルホ
ン酸塩、イゲポンT、エアロゾルOT、リグニン
スルホン酸塩の如きスルホン酸塩系アニオン活性
剤、高級アルコールリン酸エステル塩、リン酸エ
ステル塩系のアニオン活性剤などである。これら
の活性剤は通常0.01〜1重量%の範囲で使用され
る。
処理液を繊維に付着させる方法としてはパツド
法、浸染法、噴露法、塗布法等適宜の手段で実施
することが出来る。
処理液を付着させた繊維は次いで乾燥すること
なく、例えば巻き込んでフイルム等でカバーして
水分の蒸散を防止した状態で室温(例えば10℃以
上、40℃未満)下に放置する。放置時間は室温や
加工剤組成により異なるが、一般には24時間以上
が好ましい。また、放置時には樹脂付着斑が生じ
ないよう回転等を与えることが望ましい。
次いでアニオン界面活性剤とアルカリの組成わ
せで、加熱ソーピング、水洗、乾燥、仕上セツト
等を行つて最終製品とする。
以上の如き本発明の方法によれば色相のくすみ
を生ずることなく、洗濯耐久性に優れた防融性あ
る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柔軟な製品とな
しうる。これ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、防融効果の洗濯耐久性の向上に寄与するので
ある。
次に、本発明の実施例を示す。
実施例における試験結果は次の方法によるもの
である。
樹脂付着率
未処理布に対する処理布の重量増加率を示す。
色相変化
分光光度計により測定した処理布と未処理布の
色差△Eを示す。
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出し、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
間接触后の状態を観察する。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。
吸水性
0.03c.c.の水を滴下し、水滴が消えるまでの時間
を示す。
なお、防融性及び吸水性の洗濯耐久性を同時に
試験したが、その洗濯条件は次の通りである。
洗濯機:日立製作所製の日立PF2000青空、標準
サイクル(洗浄12分、その他15分の計25分)使
用。
洗濯試料重量:720g
洗剤量:36g
水 量:36
温 度:40℃
洗濯回数:10回
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表に示す
組成の水性処理液を100重量%になる様にパツド
し、そのままロールに巻取りポリプロピレンフイ
ルムでシールし水の蒸散を防止し、ロールを低速
で回転させながら第1表に示した時間放置した。
しかる後アニオン界面活性剤1g/、炭酸ソー
ダ0.5g/を含む60℃の洗浄液でソーピングし、
水洗、乾燥した。処理布については樹脂付着率、
色差、吸水性、防融性、を測定した結果を第2表
に示す。
第1表、及び第2表の結果から明らかな如く、
本発明の方法ではすぐれた防融性を示し、その洗
濯耐久性も十分であり、また白化現象もほとんど
みられず、従つて色の鮮明性低下もわずかであ
る。さらに耐久性ある吸水性も発現する。一方比
較例No.9では防融性は付与されるものの、白化
現象が生じ色の鮮明性が低下しており、十分な吸
水性も発現していない。また、比較例No.10、
No.11で明らかな如くメラミン誘導体100重量部
に対するポリアクリル酸の使用比率が5重量部以
下になると防融性、白化防止性、吸水性とも満足
な結果が得られず、逆に40重量部以上になると吸
水性、白化防止性の効果は認められるが、防融性
が低下する。
The present invention relates to an improved melt-proofing method for 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. Can be mentioned. 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; Tokkosho adding anionic surfactant to mixed aqueous solution
The method described in Japanese Patent No. 49-32760 is known.
Furthermore, a mixed aqueous solution of a melamine derivative, an acidic catalyst, and an anionic surfactant is attached to the JP-B 53-7, which is left at room temperature to prevent water evaporation.
Methods such as those described in Japanese Patent No. 19719 are also known, but although the fibers obtained by these methods have melt-proofing properties, they have the disadvantage of causing a change in the hue of the processed cloth, that is, a so-called whitening phenomenon. In addition, there is also a method described in JP-A-54-93198, in which an aqueous solution containing a melamine derivative is applied without a catalyst and then heat treated, and a method described in JP-A-54-93198, in which an aqueous solution containing a water-soluble polymer compound and a melamine derivative is applied without a catalyst and then heat treated. Methods described in JP-A-54-106692 are also known, but although these methods alleviate the whitening phenomenon, they lack adhesion and reproducibility, require high-pressure equipment, and cannot obtain a sufficient amount of adhesion. As a result, there was a drawback that the washing resistance of the anti-melt effect deteriorated. Therefore, we have conducted extensive research to improve these drawbacks and provide a melt-proofing method for synthetic fibers that does not cause the so-called whitening phenomenon, has clear color tone, and has wash resistance. Special application was first made in 1984.
Patent application No. 123474 was filed, but this method used a treatment solution containing a melamine derivative, a salt of polyacrylic acid, and an inorganic acid salt catalyst, and required moist heat treatment. Although this method achieved the desired effect,
We have continued our research to find out whether it is possible to obtain the desired effect more efficiently and at a lower cost, and have achieved the present invention. The purpose of the present invention is to provide synthetic fibers with wash-resistant and melt-proofing properties without the need for inorganic acid salt catalysts or moist heat treatment, by an industrially very easy and inexpensive method, and without causing the so-called whitening phenomenon. and to provide a method capable of imparting water absorbency. The method of the present invention involves applying an aqueous treatment liquid containing a melamine derivative and at least one hydrophilic polymer selected from the group consisting of polyacrylic acid, polymethacrylic acid, and salts thereof to synthetic fibers, and then It is characterized by being left at room temperature in a state that prevents transpiration. Synthetic fibers applicable to the present invention include polyester fibers, polyamide fibers, acrylic fibers, polyolefin fibers, etc., and these can be used in any form such as cotton, yarn, woven or knitted fabrics, or nonwoven fabrics. Furthermore, these synthetic fibers can be used by blending, interweaving, or interweaving with each other or with non-thermofusible fibers such as natural fibers. 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 bismethoxymethylmethylolmelamine. Among these, it is particularly preferable to use hexamethylolmelamine, pentamethylolmelamine, and trimethylolmelamine. The salts of polyacrylic acid and polymethacrylic acid used in the present invention are water-soluble salts, and are preferably alkali metal salts or ammonium salts. Polyacrylic acid and the like may be not only linear polymers but also crosslinked and branched ones. Regarding the degree of polymerization of polyacrylic acid, for example, if the solid content is 40%, the viscosity is
20,000 cps or less, preferably 2,000 cps or less is easy to use, but it is not limited to this. In the method of the present invention, a melamine derivative compound and a hydrophilic polymer are applied to synthetic fibers as an aqueous treatment solution, mainly an aqueous solution. The concentration of the melamine derivative compound in this treatment solution varies depending on the texture of the target fiber, processing conditions, type of hydrophilic polymer, concentration, etc., but is usually 3 to 20% by weight, preferably 5% by weight.
~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.
0.5-5% by weight is preferred. The amount of hydrophilic polymer is usually 5 parts by weight per 100 parts by weight of melamine derivative in the treatment solution.
It is used in a proportion of ~40 parts by weight, preferably 10-35 parts by weight. When used within this range, the effect of preventing whitening and improving the washing durability of anti-melting properties is remarkable. Note that it is easier to use the treatment liquid at room temperature in terms of operation. A surfactant may be added to the treatment liquid of the present invention, and the surfactant is preferably an anionic surfactant. The anionic surfactant promotes the formation of a film formed by the melamine derivative and the hydrophilic polymer, and a nonionic surfactant may be used in combination to promote permeability. Anionic surfactants include: For example, soap, carboxylic acid anion activator of sarcosinate, higher alcohol sulfate ester salt, sulfated oil,
Anion activators based on sulfate ester salts such as sulfated fatty acid esters and sulfated olefins, sulfonate anion activators such as alkylbenzene sulfonates, alkylnaphthalene sulfonates, Igepon T, Aerosol OT, and lignosulfonates. , higher alcohol phosphate ester salts, phosphate ester salt-based anion activators, and the like. These active agents are generally used in an amount of 0.01 to 1% by weight. The treatment liquid can be applied to the fibers by any suitable method such as a pad method, a dyeing method, a spray method, or a coating method. The fibers to which the treatment liquid has been applied are then left at room temperature (eg, 10° C. or higher, but lower than 40° C.) without drying, for example, by rolling them up and covering them with a film or the like to prevent moisture evaporation. The standing time varies depending on the room temperature and composition of the processing agent, but is generally preferably 24 hours or more. In addition, it is desirable to rotate the product when it is left to prevent resin adhesion spots from occurring. Next, by combining an anionic surfactant and an alkali, heat soaping, water washing, drying, finishing setting, etc. are performed to obtain a final product. According to the method of the present invention as described above, it is possible to easily obtain a synthetic fiber product with excellent washing durability and melt resistance without causing dullness of hue.
Furthermore, the texture of the product does not harden due to processing and can be made into a flexible product. This is because hydrophilic polymers such as polyacrylic acid are crosslinked with melamine derivatives, contributing to prevention of whitening, improvement of texture, and improvement of washing durability due to anti-melting effect. Next, examples of the present invention will be shown. The test results in the examples are based on the following method. Resin adhesion rate Indicates the weight increase rate of treated fabric compared to untreated fabric. Hue Change The color difference ΔE between treated and untreated fabrics measured using a spectrophotometer is shown. 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 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 Hold a lit cigarette vertically against a cloth under its own weight and observe the condition after contact for 30 seconds. The numbers indicate the size (diameter) of the melt pores. The numbers in parentheses indicate the size (diameter) of the focus. Water Absorption: 0.03cc of water is dropped and the time required for the water droplets to disappear is shown. In addition, the washing durability of melt-proofing property and water absorption property was tested at the same time, and the washing conditions were as follows. Washing machine: Hitachi PF2000 Aozora manufactured by Hitachi, standard cycle (12 minutes for washing and 15 minutes for other operations, total 25 minutes). Washing sample weight: 720g Detergent amount: 36g Water amount: 36 Temperature: 40°C Number of washes: 10 times Example 1 Polyester gear bagine (fabric weight 218 g/m 2 ) dyed navy blue with disperse dye by a conventional method was washed. An aqueous treatment solution having the composition shown in Table 1 was padded to 100% by weight, rolled up into a roll, sealed with a polypropylene film to prevent water evaporation, and while rotating the roll at low speed, the solution shown in Table 1 was applied. I left it for a while.
After that, it was soaped with a cleaning solution at 60℃ containing 1 g of anionic surfactant and 0.5 g of soda carbonate.
Washed with water and dried. For treated cloth, resin adhesion rate,
Table 2 shows the results of measuring color difference, water absorption, and melt resistance. As is clear from the results in Tables 1 and 2,
The method of the present invention exhibits excellent melt resistance, sufficient washing durability, almost no whitening phenomenon, and therefore only a slight decrease in color clarity. It also exhibits durable water absorbency. On the other hand, in Comparative Example No. 9, although melt-proofing properties were imparted, a whitening phenomenon occurred and the clarity of the color decreased, and sufficient water absorbency was not developed. Also, comparative example No. 10,
As is clear from No. 11, if the ratio of polyacrylic acid to 100 parts by weight of the melamine derivative is less than 5 parts by weight, satisfactory results cannot be obtained in terms of melt resistance, anti-whitening properties, and water absorption; If the temperature exceeds that level, water absorption and anti-whitening effects can be observed, but the melt resistance decreases.
【表】【table】
【表】【table】
【表】
実施例 2
ナイロン編物(目付340g/m2)に実施例1No.1
の処理液を100重量%施与し、そのままロールに
巻取り、ポリプロピレンフイルムでシールし水分
の蒸散を防止した状態で、ロールを低速で回転さ
せながら20℃の恒温室で48時間放置した。しかる
後、アニオン界面活性剤1g/、炭酸ソーダ0.5
g/を含む60℃の洗浄液でソーピングし、水洗
して乾燥した布は、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。ま
た、0.03c.c.の水滴を布上に落すと11秒で浸透し
た。これに対して、未処理布は5秒の煙草接触で
3mmの開孔が、10秒の接触で7mmの開孔が見られ
た。又0.03c.c.の水滴を布上に落すと水滴が消える
まで30秒かかつた。[Table] Example 2 Example 1 No.1 on nylon knitted fabric (basis weight 340g/m 2 )
100 wt. After that, anionic surfactant 1g/, soda carbonate 0.5
Cloths that were soaped with a 60°C cleaning solution containing g/, washed with water, and dried had no dull color, no pores were observed in the cigarette contact test, and the marks were small. Additionally, when a 0.03cc water droplet was dropped on cloth, it penetrated in 11 seconds. On the other hand, in the untreated cloth, pores of 3 mm were observed after 5 seconds of contact with a cigarette, and 7 mm of pores were observed after 10 seconds of contact. Also, when a 0.03cc water droplet was dropped on a cloth, it took 30 seconds for the droplet to disappear.
Claims (1)
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、100:5〜40の重量比率で、含有する水
性処理液を付着させた後、水分の蒸散を防止した
状態で室温に放置することを特徴とする合成繊維
の防融吸水加工方法。 2 処理液が界面活性剤を含む特許請求の範囲第
1項記載の加工方法。 3 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項又は第2項記載の
加工方法。 4 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
リスメトキシメチロールメラミンである特許請求
の範囲第3項記載の加工方法。 5 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4項いずれか1項記載の加
工方法。[Scope of Claims] 1 Synthetic fibers containing (a) a melamine derivative, and (b) at least one hydrophilic polymer selected from the group consisting of polyacrylic acid, polymethacrylic acid, and salts thereof, 100: 1. A method for melt-proofing and water-absorbing synthetic fibers, which comprises applying an aqueous treatment liquid at a weight ratio of 5 to 40, and then allowing the fibers to stand at room temperature while preventing moisture evaporation. 2. The processing method according to claim 1, wherein the processing liquid contains a surfactant. 3. The processing method according to claim 1 or 2, wherein the melamine derivative is a methylol derivative of melamine. 4. The processing method according to claim 3, wherein the methylol derivative of melamine is hexamethylolmelamine, pentamethylolmelamine or trismethoxymethylolmelamine. 5. The processing method according to any one of claims 1 to 4, wherein the salts of polyacrylic acid and polymethacrylic acid are alkali metal salts or ammonium salts.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21587282A JPS59106578A (en) | 1982-12-07 | 1982-12-07 | Melt-proof and water absorbing processing of synthetic fiber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21587282A JPS59106578A (en) | 1982-12-07 | 1982-12-07 | Melt-proof and water absorbing processing of synthetic fiber |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59106578A JPS59106578A (en) | 1984-06-20 |
| JPS6143468B2 true JPS6143468B2 (en) | 1986-09-27 |
Family
ID=16679657
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP21587282A Granted JPS59106578A (en) | 1982-12-07 | 1982-12-07 | Melt-proof and water absorbing processing of synthetic fiber |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59106578A (en) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5823971A (en) * | 1981-08-05 | 1983-02-12 | カネボウ株式会社 | Melt-proof process of synthetic fiber |
-
1982
- 1982-12-07 JP JP21587282A patent/JPS59106578A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59106578A (en) | 1984-06-20 |
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