JPH0364515A - Polyvinyl chloride-based fiber and its production - Google Patents
Polyvinyl chloride-based fiber and its productionInfo
- Publication number
- JPH0364515A JPH0364515A JP19985289A JP19985289A JPH0364515A JP H0364515 A JPH0364515 A JP H0364515A JP 19985289 A JP19985289 A JP 19985289A JP 19985289 A JP19985289 A JP 19985289A JP H0364515 A JPH0364515 A JP H0364515A
- Authority
- JP
- Japan
- Prior art keywords
- spinning
- vinyl
- weight
- polyvinyl chloride
- fibers
- 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.)
- Pending
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 34
- 229920000915 polyvinyl chloride Polymers 0.000 title claims description 15
- 239000004800 polyvinyl chloride Substances 0.000 title claims description 15
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 238000009987 spinning Methods 0.000 claims abstract description 22
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims abstract description 11
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 9
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 9
- 238000000578 dry spinning Methods 0.000 claims abstract description 7
- 239000003960 organic solvent Substances 0.000 claims abstract description 6
- 238000002166 wet spinning Methods 0.000 claims abstract description 6
- 239000000463 material Substances 0.000 abstract description 18
- 229920001577 copolymer Polymers 0.000 abstract description 6
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 abstract description 4
- 239000005011 phenolic resin Substances 0.000 abstract description 4
- 229920001568 phenolic resin Polymers 0.000 abstract description 4
- 239000004745 nonwoven fabric Substances 0.000 description 11
- 239000000853 adhesive Substances 0.000 description 10
- 230000001070 adhesive effect Effects 0.000 description 9
- 239000002904 solvent Substances 0.000 description 8
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- -1 polyethylene Polymers 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000011550 stock solution Substances 0.000 description 3
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
Landscapes
- Artificial Filaments (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、熱接着性を有するポリ塩化ビニル系繊維及び
その製造法に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a polyvinyl chloride fiber having thermal adhesive properties and a method for producing the same.
(従来の技術)
電気絶縁性、機械的強さ、耐熱性、耐湿・耐水性が要求
される分野に釦ける各種成形品、積層品、無機・有機質
材料結合材等の用途に供されるフェノ−μ樹脂材料は、
ともすればその機能面のみが優先される傾向にあり、意
匠性に乏しいのが現状である。(Conventional technology) Phenomena is used for various molded products, laminated products, inorganic/organic material binding materials, etc. in fields that require electrical insulation, mechanical strength, heat resistance, moisture resistance, and water resistance. −μ resin material is
At present, there is a tendency for only the functional aspects to be prioritized, and the design quality is lacking.
一方、フェノール樹脂材料に対する溶液、エマμジョン
又は粉末の接着剤として、塩化ビニル、酢酸ビニル及び
主鎖及び/又は側鎖の一部にヒドロキシル基を有するビ
ニル誘導体の三元共重合物が使われている。On the other hand, a terpolymer of vinyl chloride, vinyl acetate, and a vinyl derivative having a hydroxyl group in a part of the main chain and/or side chain is used as a solution, emulsion, or powder adhesive for phenolic resin materials. ing.
(発明が解決しようとする課題)
フェノール樹脂材料のテクスチャーを改善スる一つの手
段として不織布を組合せてファブリック様の外観を付与
することにより高級感を顕出し、意匠性に優れた製品を
得ることが出来る。(Problems to be Solved by the Invention) As a means of improving the texture of phenolic resin materials, it is possible to obtain a product with a high-class feel and excellent design by combining non-woven fabrics to give a fabric-like appearance. I can do it.
一方、近年不織布はその製造技術の進歩にょり低コスト
化し、熱接着用途に供するのに適したポリエチレン、ポ
リプロピレン、ポリエステμ、ナイロン系の熱接着性繊
維と、不織布の主体をなす繊維との混用不織布について
も多種開発されている。このように熱接着性の異なる繊
維を混合することにより、熱接着性繊維のみを用いた場
合に較べ熱接着後もファブリック様で存在するという利
点が挙げられる。それに加えて、不織布の構成比、構造
等を加減することにより不織布そのものに要求される強
度等の物性がコントロールし易くなり、しかもエンボス
加工などによシ外観や風合いなどのテクスチャーが、多
様性に富む、付加値価の高いものを得ることが可能であ
る。On the other hand, in recent years, the cost of nonwoven fabrics has become lower due to advances in manufacturing technology, and the use of a mixture of thermoadhesive fibers such as polyethylene, polypropylene, polyester μ, and nylon, which are suitable for thermal bonding purposes, and the fibers that form the main body of nonwoven fabrics. Various types of nonwoven fabrics have also been developed. By mixing fibers with different thermal bonding properties in this way, there is an advantage that the fiber remains in a fabric-like state even after thermal bonding, compared to the case where only heat bondable fibers are used. In addition, by adjusting the composition ratio, structure, etc. of the nonwoven fabric, it becomes easier to control the physical properties such as strength required of the nonwoven fabric itself, and textures such as appearance and texture can be varied by embossing etc. It is possible to obtain products with high added value.
しかしながら従来から知られているポリエチレン、ポリ
プロピレン、ポリエステμ等の熱接着性繊維は、自己接
着性は有するもののフェノ−μ樹脂材料への接着能を持
たないためフェノール樹脂材料との接着には、他に接着
剤を使用するか、成るいは接着の機能を有する熱接着性
繊維を新たに混合しなければならず加工性及びコヌト面
で問題がある。従って、製品のテクスチャー改善の要求
から、フェノ−p樹脂材料への接着性能を有する新たな
熱接着性繊維の開発が望まれていた。However, conventionally known heat-adhesive fibers such as polyethylene, polypropylene, and polyester-μ have self-adhesive properties but do not have the ability to adhere to phenol-μ resin materials. It is necessary to use an adhesive or to newly mix heat-adhesive fibers with an adhesive function, which poses problems in terms of processability and consistency. Therefore, in order to improve the texture of products, it has been desired to develop a new thermoadhesive fiber capable of adhering to pheno-p resin materials.
本発明は、従来から溶液エマルジョン又は粉末接着剤と
しては知られていた塩化ビニル、酢酸ビニル及び主鎖及
び/又は側鎖の一部にヒドロキV/L/基を有するビニ
ル誘導体の共重合物を繊維化し、又この繊維を用いて不
織布となし、フェノ−μ樹脂材料への接着性に加えて、
近年急速に伸長しつつある塩化ビニル系樹脂材料を用い
たμmフイング材、壁装材、床材等の建築資材や自動車
内装材等への接着性をも付与し、より広範囲な接着用途
を得ると共に、その意匠性を向上させうる繊維及びその
製造法を提供するものである。The present invention uses copolymers of vinyl chloride, vinyl acetate, and vinyl derivatives having hydroxyl V/L/groups in part of the main chain and/or side chain, which have been known as solution emulsion or powder adhesives. It is made into fibers and used to make non-woven fabrics, and in addition to adhesion to pheno-μ resin materials,
It also provides adhesive properties to μm flying materials using vinyl chloride resin materials, which have been rapidly growing in recent years, to building materials such as wall covering materials and flooring materials, as well as automobile interior materials, allowing for a wider range of adhesive applications. In addition, the present invention provides a fiber that can improve its design and a method for producing the same.
又不織布とすることにより接着加工時のコストを抑える
ことができ、しかもこの不織布は取扱いが容易で加工性
に優れたものとなる繊維を提供するものである。Furthermore, by using a nonwoven fabric, the cost during adhesive processing can be reduced, and the nonwoven fabric provides a fiber that is easy to handle and has excellent processability.
(課題を解決するための手段)
本発明に塩化ビニ/I/60〜95重蛍光、酢酸ビニ/
I/2〜399重蛍光及び主鎖及び/又は側鎖の一部に
ヒドロキシル基を有するビニル誘導体0.1御10
なるポリ塩化ビニル系繊維、及び該共重合体を有機溶剤
に溶解して濃度15〜50重量係の紡蛍光液となし、紡
糸ドラフト05〜8.0の範囲にて乾式又は湿式紡糸に
て繊維化することを特徴とするポリ塩化ビニル系繊維の
製造法にある。(Means for solving the problem) The present invention includes vinyl chloride/I/60-95 double fluorescence, vinyl acetate/
I/2-399 polyvinyl chloride fiber having double fluorescence and hydroxyl groups in part of the main chain and/or side chain 0.1 to 10%, and the copolymer dissolved in an organic solvent to obtain a concentration of A method for producing polyvinyl chloride fibers, which is characterized in that it is made into fibers by dry or wet spinning at a spinning draft of 05 to 8.0 using a fluorescent spinning liquid having a weight ratio of 15 to 50.
以下、本発明について更に詳細に説明する。The present invention will be explained in more detail below.
本発明は塩化ビニルを主体とする共重合体からなる繊維
であり、塩化ビニIV60〜95重蛍光、酢酸ビニル2
〜399重量光及び主鎖及び/又は側鎖の一部にヒドロ
キシル基を有するビニル誘導体01〜10重蛍光で構成
されたポリ塩化ビニル系共重合体から繊維が形成されて
卦シ、ポリ塩化ビニル系共重合体中の酢酸ビニルの量が
2重竜係未満の場合には可塑性、溶剤に対する溶解性、
熱接着性等で不十分な点が生じ、又39.9重量係重量
光る場合には繊維としての基本的なタフネスや軟化温度
の極端な低下等の影響が出る。又、酢酸ビニルと共に共
重合される主鎖及び/又は側鎖の一部にヒドロキシル基
を有するビニル誘導体はF!を気絶縁性、機械的強さ、
耐熱性、耐湿・耐水性が要求される分野にかける各種成
形品、積層品や、無機・有機質材料結合材等の用途に供
されるフェノール樹脂材料への接着性の向上、改良に有
効な成分であり、例えばビニルアルコールや2−ヒドロ
キシプロピルアクリレート等が用いられる。とのビニル
誘導体の量が0.1重量光未満の場合には接着性の改良
効果が小さいのは当然であるが、10重量蛍光超える場
合にはより顕著な改良効果は認められない。The present invention is a fiber made of a copolymer mainly composed of vinyl chloride, vinyl chloride IV 60-95 double fluorescence, vinyl acetate 2
A fiber is formed from a polyvinyl chloride copolymer composed of ~399 weight light and a vinyl derivative having hydroxyl groups in the main chain and/or part of the side chain. When the amount of vinyl acetate in the copolymer is less than 2%, plasticity, solubility in solvents,
Insufficient thermal adhesion properties may occur, and if the weight ratio is 39.9, the basic toughness of the fiber and the softening temperature will be significantly lowered. Furthermore, vinyl derivatives having hydroxyl groups in part of the main chain and/or side chain that are copolymerized with vinyl acetate are F! The insulation properties, mechanical strength,
An effective ingredient for improving and improving the adhesion of phenolic resin materials used in various molded products and laminated products used in fields that require heat resistance, moisture resistance, and water resistance, as well as inorganic and organic material binders. For example, vinyl alcohol, 2-hydroxypropyl acrylate, etc. are used. Naturally, when the amount of the vinyl derivative is less than 0.1 weight light, the effect of improving adhesion is small, but when it exceeds 10 weight light, a more significant improvement effect is not observed.
本発明の繊維は塩化ビニル、酢酸ビニル及び主鎖及び/
又は側鎖の一部にヒドロキシル基を有するビニル誘導体
で構成されたポリ塩化ビニル系共重合体を主原料として
乾式又は湿式紡糸法によって繊維化することができる。The fibers of the present invention include vinyl chloride, vinyl acetate and the main chain and/or
Alternatively, a polyvinyl chloride copolymer composed of a vinyl derivative having a hydroxyl group in a part of the side chain can be used as a main raw material to form fibers by a dry or wet spinning method.
紡糸原液の溶剤としては、ケトン、エステル、塩素化炭
化水素等の有機溶剤が使用可能であシ、例えば酢酸エチ
μ、酢酸ブチル、アセトン、メチμエチμケトン、メチ
μイソブチμケトン、ジイソブチルケトン、エチレンジ
クロフィト、プロピレンオキサイド、ジオキサン、イソ
ホロン、ジブチμフォスファイト等が挙げられ、更には
これら以外にも貧溶媒を加えた混合溶剤の使用も可能で
ある。Organic solvents such as ketones, esters, and chlorinated hydrocarbons can be used as the solvent for the spinning stock solution, such as ethyl acetate, butyl acetate, acetone, methyμ ethylketone, methiμ isobutyμ ketone, and diisobutyl ketone. , ethylene dicrophyte, propylene oxide, dioxane, isophorone, dibutymu phosphite, etc. Furthermore, it is also possible to use a mixed solvent in which a poor solvent is added in addition to these.
紡糸原液はポリ塩化ビニル系共重合体に有機溶剤を加え
て調製される。A spinning dope is prepared by adding an organic solvent to a polyvinyl chloride copolymer.
紡糸原液中のポリ塩化ビニル系共重合体の濃度は、その
粘性から15〜50重量係、重量光くは23〜47重量
係ど重量光がよい。濃度が50重負傷光超えると粘性が
高くなり、紡糸原液の品質の均一性を保ち難く、又紡糸
口金からの吐出性も悪化し、好ましくない。一方、15
重量俤未満であると曳糸性が低く、紡糸安定性が低下す
る。The concentration of the polyvinyl chloride copolymer in the spinning dope is preferably 15 to 50% by weight, preferably 23 to 47% by weight, depending on its viscosity. If the concentration exceeds 50%, the viscosity increases, making it difficult to maintain the uniform quality of the spinning dope, and the ejection properties from the spinneret deteriorates, which is not preferable. On the other hand, 15
If it is less than the weight, the spinnability will be low and the spinning stability will be reduced.
繊維化を乾式紡糸にて行う場合には、紡糸原液を紡糸口
金から25〜140℃の加熱雰囲気中に吐出し、溶剤を
蒸発揮散させ繊維化する。When forming fibers by dry spinning, the spinning dope is discharged from a spinneret into a heated atmosphere at 25 to 140°C, and the solvent is evaporated and evaporated to form fibers.
又湿式紡糸の場合には貧溶媒又は貧溶媒と前記溶剤とか
らなる凝固液中に吐出し脱溶剤して繊維化する。この紡
糸の際の紡糸ドラフト、即ち引取シ速度に対する紡糸原
液の吐出速度の比(引取り速度/吐出速度)は、0.5
〜8.0で、0.5未満の低ドラフトでは、フィードロ
ーラーで引取る1での乾燥雰囲気中で糸条のゆれ等を誘
い、紡糸安定性が低下し好ましくない。本発明では0.
5〜8.0の紡糸ドラフトの範囲内で望ましい糸物性と
、紡糸安定性が十分確保される。In the case of wet spinning, the material is discharged into a poor solvent or a coagulating solution consisting of a poor solvent and the above-mentioned solvent to remove the solvent and form fibers. The spinning draft during this spinning, that is, the ratio of the discharge speed of the spinning dope to the take-up speed (take-up speed/discharge speed) is 0.5.
-8.0, but a low draft of less than 0.5 is undesirable because it invites wobbling of the yarn in the drying atmosphere at step 1 taken up by the feed roller and reduces spinning stability. In the present invention, 0.
Desirable yarn physical properties and spinning stability can be sufficiently ensured within the range of spinning draft of 5 to 8.0.
以上の様にして本発明のポリ塩化ビニル系繊維を得るこ
とができる。The polyvinyl chloride fiber of the present invention can be obtained in the manner described above.
(実施例) 以下、実施例により、本発明を具体的に説明する。(Example) Hereinafter, the present invention will be specifically explained with reference to Examples.
実施例
塩化ビニル92重量光、酢酸ビニル3重量係、及びビニ
ルアルコー/115重量光からなる重合度430の三元
共重合体を、塩化メチレン91重量係及びメタノール9
重量光からなる混合溶剤に溶解し、濃度30重重量光調
製して紡糸原液とした。この紡糸原液を60℃に加熱し
、孔径49μmの紡糸口金から第1表の条件下で乾式紡
糸を実施した。その結果を第1図に示す。Example: A terpolymer with a degree of polymerization of 430 consisting of vinyl chloride (92 parts by weight), vinyl acetate (3 parts by weight), and vinyl alcohol/115 parts by weight (light parts) was mixed with methylene chloride (91 parts by weight) and methanol (91 parts by weight).
It was dissolved in a mixed solvent consisting of heavy light, and the concentration was adjusted to 30% light to obtain a spinning stock solution. This spinning stock solution was heated to 60° C., and dry spinning was performed under the conditions shown in Table 1 through a spinneret with a hole diameter of 49 μm. The results are shown in FIG.
この様にして得られた繊維を不織布と々し、各種材料と
の接着テストを行なった結果を第2表に示す。○印は接
着性の良好なもの、×印は接着性の不良なものを表わす
。The fibers thus obtained were made into nonwoven fabrics and tested for adhesion to various materials. The results are shown in Table 2. The ○ mark indicates good adhesion, and the x mark indicates poor adhesion.
第1表
(発明の効果)
本発明のポリ塩化ビニル系繊維は単独で、又はアクリμ
繊維やその他の繊維との混合により不織布となすことが
でき、ポリ塩化ビニル樹脂材料への基本的々接着性は勿
論のこと、フェノ−μ樹脂材料への優れた接着性を有す
るものであシ、接着分野での用途が拡大し、実用上大い
に有益で意義あるものである。Table 1 (Effects of the Invention) The polyvinyl chloride fiber of the present invention can be used alone or with acrylic μ
It can be made into a nonwoven fabric by mixing with fibers or other fibers, and it has excellent adhesion to pheno-μ resin materials as well as basic adhesion to polyvinyl chloride resin materials. , its applications in the field of adhesives have expanded, and it is of great practical use and significance.
第1図は延伸率と乾強力・乾伸度との関係図である。 FIG. 1 is a diagram showing the relationship between stretching ratio and dry strength/dry elongation.
Claims (2)
9.9重量%及び主鎖及び/又は側鎖の一部にヒドロキ
シル基を有するビニル誘導体0.1〜10重量%で構成
されたポリ塩化ビニル系共重合体からなるポリ塩化ビニ
ル系繊維。(1) Vinyl chloride 60-95% by weight, vinyl acetate 2-3
A polyvinyl chloride fiber made of a polyvinyl chloride copolymer composed of 9.9% by weight and 0.1 to 10% by weight of a vinyl derivative having a hydroxyl group in a part of the main chain and/or side chain.
9.9重量%及び主鎖及び/又は側鎖の一部にヒドロキ
シル基を有するビニル誘導体0.1〜10重量%で構成
されたポリ塩化ビニル系共重合体を有機溶剤に溶解して
濃度15〜50重量%の紡糸原液となし、紡糸ドラフト
0.5〜8.0の範囲にて乾式又は湿式紡糸にて繊維化
することを特徴とするポリ塩化ビニル系繊維の製造法。(2) Vinyl chloride 60-95% by weight, vinyl acetate 2-3
A polyvinyl chloride copolymer composed of 9.9% by weight and 0.1 to 10% by weight of a vinyl derivative having a hydroxyl group in a part of the main chain and/or side chain is dissolved in an organic solvent to a concentration of 15%. A method for producing polyvinyl chloride fibers, which comprises using a spinning dope of ~50% by weight and forming fibers by dry or wet spinning at a spinning draft of 0.5 to 8.0.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19985289A JPH0364515A (en) | 1989-08-01 | 1989-08-01 | Polyvinyl chloride-based fiber and its production |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19985289A JPH0364515A (en) | 1989-08-01 | 1989-08-01 | Polyvinyl chloride-based fiber and its production |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0364515A true JPH0364515A (en) | 1991-03-19 |
Family
ID=16414725
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP19985289A Pending JPH0364515A (en) | 1989-08-01 | 1989-08-01 | Polyvinyl chloride-based fiber and its production |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0364515A (en) |
-
1989
- 1989-08-01 JP JP19985289A patent/JPH0364515A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR102566514B1 (en) | Biodegradable Textiles, Masterbatches, and Methods of Making Biodegradable Fibers | |
DE60223022T2 (en) | FIBERS OF THICKNESS AND POLYMERS | |
JP4119756B2 (en) | Fibers containing starch and biodegradable polymers | |
EP1560954B1 (en) | Compositions and processes for reducing water solubility of a starch component in a multicomponent fiber | |
EP1397539B1 (en) | Multicomponent fibers comprising starch and polymers | |
US4356229A (en) | Bonded nonwoven fabrics suitable for diaper coverstock | |
JPH0120249B2 (en) | ||
AU2002309682A1 (en) | Fibers comprising starch and polymers | |
JP6548634B2 (en) | Polyester binder fiber | |
EP0311860B1 (en) | Nonwoven fabric made of heat bondable fibers | |
US3125462A (en) | Textile fabrics treated with ethylene- | |
EP0184153B1 (en) | Formaldehyde-free latex and fabrics made therewith | |
JPH0364515A (en) | Polyvinyl chloride-based fiber and its production | |
US20060036014A1 (en) | Wallcovering coating | |
JPH01229899A (en) | Composition for binder fiber | |
JPH04174719A (en) | Conjugate yarn | |
DE2742208A1 (en) | FIBER FLEECE AND METHOD FOR THE PRODUCTION THEREOF | |
CN110241477A (en) | Antibacterial pro-skin polypropylene filament yarn and preparation method thereof | |
JP2006144199A (en) | Heat bonding conjugated fiber and fiber structure and composite molded product of object of different kind using the same | |
JPH06200409A (en) | Heat accumulating acrylic synthetic yarn and its production | |
JPS6135320B2 (en) | ||
JPS5810493B2 (en) | Kami Oyobi Fushiyokufuyousenino Seizouhou | |
JPH02145810A (en) | Polyvinyl chloride fiber and production thereof | |
JPH0782607A (en) | Heat storage acrylic synthetic fiber and its production | |
JP2002069744A (en) | Thermoadhesive binder fiber |