JPS5845481B2 - Seniseizouhou - Google Patents
SeniseizouhouInfo
- Publication number
- JPS5845481B2 JPS5845481B2 JP15226675A JP15226675A JPS5845481B2 JP S5845481 B2 JPS5845481 B2 JP S5845481B2 JP 15226675 A JP15226675 A JP 15226675A JP 15226675 A JP15226675 A JP 15226675A JP S5845481 B2 JPS5845481 B2 JP S5845481B2
- Authority
- JP
- Japan
- Prior art keywords
- fibers
- fiber
- synthetic resin
- fatty acid
- nozzle hole
- 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
- Artificial Filaments (AREA)
- Multicomponent Fibers (AREA)
- Spinning Methods And Devices For Manufacturing Artificial Fibers (AREA)
Description
【発明の詳細な説明】 本発明は繊維の新規な製造法に関するものである。[Detailed description of the invention] The present invention relates to a novel method for producing fibers.
更に詳しくは、繊維形成能を有する合成樹脂と高級脂肪
酸金属塩を混合後、押出機により1個のノズル孔から複
数本の繊維を連続的に製造する方法に関するものである
。More specifically, the present invention relates to a method for continuously producing a plurality of fibers from one nozzle hole using an extruder after mixing a synthetic resin having fiber-forming ability and a higher fatty acid metal salt.
従来、繊維の製造方法には溶融紡糸法、乾式紡糸法およ
び湿式紡糸法等があるが、いずれの場合もノズル孔の径
は1間以下の細孔を多数設け、1個の孔から1本の繊維
を紡糸する方法が採用されている。Traditionally, fiber manufacturing methods include melt spinning, dry spinning, and wet spinning, but in all of these methods, the nozzle hole has a large number of pores with a diameter of 1 mm or less, and one A method of spinning fibers is adopted.
本発明者らは、スクリュ一式押出機を用いて成形可能な
合成樹脂と該合成樹脂に対して20〜300重量%の高
級脂肪酸金属塩の混合物から、連続的にしかも1本の太
いノズル孔から数百本〜数千水の繊維を得ることができ
るという新事実を見出し、本発明に到達したものである
。The present inventors have continuously produced a mixture of a synthetic resin that can be molded using a single-screw extruder and a higher fatty acid metal salt of 20 to 300% by weight based on the synthetic resin, and from a single thick nozzle hole. The present invention was achieved by discovering a new fact that several hundred to several thousand water fibers can be obtained.
すなわち本発明は、繊維形成能を有する合成樹脂と該合
成樹脂に対して20〜300重量%の高級脂肪酸金属塩
とを十分混合し、スクリュー押出機により加熱溶融しな
がら1個のノズル孔を通して数百本〜数千水からなる繊
維を束状に連続的に製造する方法である。That is, in the present invention, a synthetic resin having a fiber-forming ability and a higher fatty acid metal salt in an amount of 20 to 300% by weight based on the synthetic resin are thoroughly mixed, and the mixture is heated and melted using a screw extruder and passed through one nozzle hole in several numbers. This is a method of continuously producing bundles of 100 to several thousand water fibers.
本発明に使用される高級脂肪酸金属塩は、飽和脂肪酸と
してカプリン酸、ステアリン酸等、不飽和脂肪酸として
オレイン酸、リノール酸、リルン酸等を挙げることがで
き、これら高級脂肪酸に金属を反応せしめて塩の形とし
たものである。The higher fatty acid metal salts used in the present invention include saturated fatty acids such as capric acid and stearic acid, and unsaturated fatty acids such as oleic acid, linoleic acid, and lylunic acid. It is in the form of salt.
塩として結合した金属の一例を挙げると、亜鉛・アルミ
ニウム・カルシウム・銀・銅・リチウム・タリウム・ニ
ッケル・バリウム・マグネシウム・鉛・鉄等がある。Examples of metals combined as salts include zinc, aluminum, calcium, silver, copper, lithium, thallium, nickel, barium, magnesium, lead, and iron.
しかし、これらに限定されるものではない。However, it is not limited to these.
本発明に用いられる合成樹脂には、広く繊維形成能を有
する樹脂が使用できる。As the synthetic resin used in the present invention, a wide variety of resins having fiber-forming ability can be used.
一例を挙げるとナイロン66、ナイロン6等のポリアミ
ド系合成樹脂、ポリエステル系合成樹脂、ポリオレフィ
ン系合成樹脂、ポリ塩化ビニル系合成樹脂、ポリ塩化ビ
ニリデン系合成樹脂、ポリスチレン系合成樹脂などがあ
る。Examples include polyamide synthetic resins such as nylon 66 and nylon 6, polyester synthetic resins, polyolefin synthetic resins, polyvinyl chloride synthetic resins, polyvinylidene chloride synthetic resins, and polystyrene synthetic resins.
しかし、これだけに限定されるものではない。However, it is not limited to this.
これら高級脂肪酸金属塩の一種又は二種以上とと成樹脂
の一種又は二種以上とを組合わせても使用できる。It is also possible to use a combination of one or more of these higher fatty acid metal salts and one or more of the synthetic resins.
高級脂肪酸金属塩の使用量は合成樹脂に対して20〜3
00重量%、好ましくは50〜150重量%使用が適当
である。The amount of higher fatty acid metal salt used is 20 to 3 per synthetic resin.
It is appropriate to use 00% by weight, preferably 50 to 150% by weight.
20重量%より少ないと、一度に多数の繊維が得難くな
り、また300重量%より多いと、ノズル孔よりの樹脂
の押出しがし難くなるからである。If it is less than 20% by weight, it will be difficult to obtain a large number of fibers at once, and if it is more than 300% by weight, it will be difficult to extrude the resin through the nozzle hole.
樹脂の加熱温度範囲は、合成樹脂および高級脂肪酸金属
塩の軟化点あるいは融点により異なるが、100〜30
0℃好ましくは130〜250’Cの範囲に加熱しなが
ら押出しすると良い結果が得られる。The heating temperature range of the resin varies depending on the softening point or melting point of the synthetic resin and higher fatty acid metal salt, but is 100 to 30
Good results can be obtained by extruding while heating at 0°C, preferably in the range of 130-250'C.
本発明による1本の太いノズル孔から多数の繊維が連続
的に得られる機構は次のように考えられる。The mechanism by which a large number of fibers can be continuously obtained from one thick nozzle hole according to the present invention is considered as follows.
すなわち、合成樹脂と高級脂肪酸金属塩の混合物は、ス
クリュー押出機に連続的に供給され、加熱溶融されてダ
イス部に移動してくる。That is, a mixture of synthetic resin and higher fatty acid metal salt is continuously supplied to a screw extruder, heated and melted, and transferred to a die section.
ここでダイスの形状は、テーパーがついていて、さらに
ノズル孔では平行部分すなわちランドがある。Here, the shape of the die is tapered, and furthermore, there is a parallel portion, that is, a land at the nozzle hole.
繊維化されるのもこのランドに入ってからであり、溶融
した樹脂を溶融した高級脂肪酸金属塩が多分子層状に被
覆し、ランドの部分でこの材料の移動速度は加速さえ、
樹脂は繊維化され、繊維化された樹脂表面には溶融した
高級脂肪酸金属塩が多分子層状に被覆するので、1個の
ノズル孔から多数の繊維が融着されずにバラバラの状態
で得られるものと考えられる。It is only after entering this land that the molten resin is made into fibers, and the molten resin is coated with a multi-layered layer of molten higher fatty acid metal salt, and the movement speed of this material is accelerated in the land area.
The resin is made into fibers, and the surface of the fiberized resin is coated with a multilayered layer of molten higher fatty acid metal salts, so that a large number of fibers can be obtained from one nozzle hole in a separate state without being fused. considered to be a thing.
以下本発明を実施例によって説明する。The present invention will be explained below with reference to Examples.
実施例 1
ステアリン酸カルシウム200gとポリスチレン300
gをヘンシェルミキサーを用いて常温で十分混合した。Example 1 200g of calcium stearate and 300g of polystyrene
g were thoroughly mixed at room temperature using a Henschel mixer.
該混合物を401rL1ftスクリユ一押出機に供給し
、220℃に加熱しながら押出しを行い繊維化させた。The mixture was supplied to a 401rL 1ft screw extruder and extruded while heating at 220°C to form fibers.
ノズル孔の直径は4間を用いた。このようにして得られ
た多数の繊維から戒る束状の繊維は棒状であった。The diameter of the nozzle hole was 4 mm. The bundle-shaped fibers obtained from the large number of fibers thus obtained were rod-shaped.
該束状の繊維のうちステアリン酸カルシウムを温水中で
溶解して取除くと、ポリスチレン繊維束が得られた。When the calcium stearate of the fiber bundle was removed by dissolving it in hot water, a polystyrene fiber bundle was obtained.
この繊維の太さは平均3μであり、繊維束は約1.10
0本のポリスチレン繊維から戒っていた。The average thickness of these fibers is 3μ, and the fiber bundle is approximately 1.10μ.
I was warned not to use 0 polystyrene fibers.
この束状の繊維は、繊維間の融着は全くなかった。There was no fusion between the fibers in this bundle of fibers.
実施例 2
ステアリン酸ナトリウム400gとポリエチレンテレフ
タレート300gをヘンシェルミキサーを用いて常温で
十分混合した。Example 2 400 g of sodium stearate and 300 g of polyethylene terephthalate were thoroughly mixed at room temperature using a Henschel mixer.
該混合物を40關スクリユ一押出機に供給し、250′
Cに加熱しながら押出しを行い繊維化させた。The mixture was fed into a 40 screw extruder and
Extrusion was performed while heating at C to form fibers.
ノズル孔の直径は21nmを用いた。The diameter of the nozzle hole was 21 nm.
このようにして得られた多数の繊維から戒る束状の繊維
は棒状であった。The bundle-shaped fibers obtained from the large number of fibers thus obtained were rod-shaped.
該束状のステアリン酸ナトリウムを含む棒状物を800
0の温水中でステアリン酸すl−IJウムを溶解除去す
ると、ポリエチレンテレフタレート繊維が得られた。800 sticks containing the bundled sodium stearate
Polyethylene terephthalate fibers were obtained by dissolving and removing the sodium stearate in warm water of 0.0 °C.
この繊維の太さは平均2μであり、繊維束は約800本
のポリエチレンテレフタレート繊維から成っていた。The fibers had an average thickness of 2 μm, and the fiber bundle consisted of about 800 polyethylene terephthalate fibers.
この束状の繊維は、繊維間の融着は全くなかった。There was no fusion between the fibers in this bundle of fibers.
以上の実施例かられかるように、繊維形成能を有する合
成樹脂と高級脂肪酸金属塩を混合後、スクリュー押出機
を用いて加熱溶融せしめ、1個のノズル孔から押出しす
ることによって多数の繊維から成る束状の繊維を連続的
に製造できるという結果を得た。As can be seen from the above examples, a synthetic resin having fiber-forming ability and a higher fatty acid metal salt are mixed, heated and melted using a screw extruder, and extruded from one nozzle hole to form a large number of fibers. The results showed that it was possible to continuously produce bundle-like fibers.
本発明は、混合機とスクリュー押出機からなる装置を用
いるだけで多数の繊維からなる束状の繊維を工業的に容
易に製造できるものである。According to the present invention, fiber bundles made of a large number of fibers can be easily manufactured industrially by simply using a device consisting of a mixer and a screw extruder.
Claims (1)
20〜300重量%の高級脂肪酸金属塩の混合物から押
出機により1個0)ノズル孔から多数の繊維を連続的に
製造する繊維製造法。1) A fiber manufacturing method in which one fiber is continuously produced from a mixture of a synthetic resin having fiber-forming ability and a higher fatty acid metal salt in an amount of 20 to 300% by weight based on the synthetic resin through a nozzle hole using an extruder. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15226675A JPS5845481B2 (en) | 1975-12-19 | 1975-12-19 | Seniseizouhou |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15226675A JPS5845481B2 (en) | 1975-12-19 | 1975-12-19 | Seniseizouhou |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5277222A JPS5277222A (en) | 1977-06-29 |
| JPS5845481B2 true JPS5845481B2 (en) | 1983-10-11 |
Family
ID=15536723
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15226675A Expired JPS5845481B2 (en) | 1975-12-19 | 1975-12-19 | Seniseizouhou |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5845481B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0298596U (en) * | 1989-01-20 | 1990-08-06 |
-
1975
- 1975-12-19 JP JP15226675A patent/JPS5845481B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0298596U (en) * | 1989-01-20 | 1990-08-06 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5277222A (en) | 1977-06-29 |
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