JPH04355196A - Pen point lead for writing utensils and production thereof - Google Patents
Pen point lead for writing utensils and production thereofInfo
- Publication number
- JPH04355196A JPH04355196A JP3157667A JP15766791A JPH04355196A JP H04355196 A JPH04355196 A JP H04355196A JP 3157667 A JP3157667 A JP 3157667A JP 15766791 A JP15766791 A JP 15766791A JP H04355196 A JPH04355196 A JP H04355196A
- Authority
- JP
- Japan
- Prior art keywords
- solvent
- fiber
- fibers
- acrylic
- nib
- 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
- 229920002972 Acrylic fiber Polymers 0.000 claims description 45
- 239000002904 solvent Substances 0.000 claims description 43
- 239000000835 fiber Substances 0.000 claims description 42
- 238000000034 method Methods 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 238000007789 sealing Methods 0.000 claims description 6
- 239000000976 ink Substances 0.000 description 17
- -1 polyurethane Chemical compound 0.000 description 10
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 238000002156 mixing Methods 0.000 description 8
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 239000004745 nonwoven fabric Substances 0.000 description 6
- 229920000573 polyethylene Polymers 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 210000002268 wool Anatomy 0.000 description 4
- 239000002131 composite material Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- JHUFGBSGINLPOW-UHFFFAOYSA-N 3-chloro-4-(trifluoromethoxy)benzoyl cyanide Chemical compound FC(F)(F)OC1=CC=C(C(=O)C#N)C=C1Cl JHUFGBSGINLPOW-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920002978 Vinylon Polymers 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000009960 carding Methods 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- VRAHSRHQTRYBJV-UHFFFAOYSA-M sodium;2-methyl-1-oxoprop-2-ene-1-sulfonate Chemical compound [Na+].CC(=C)C(=O)S([O-])(=O)=O VRAHSRHQTRYBJV-UHFFFAOYSA-M 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Pens And Brushes (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、サインペン,マーカー
等の筆記具に用いられるペン先芯およびその製法に関す
るものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a pen nib used in writing implements such as felt-tip pens and markers, and a method for manufacturing the same.
【0002】0002
【従来の技術】従来、サインペン,マーカー等の筆記具
のペン先芯には、羊毛フエルトが用いられている。また
、最近では、ビニロン,ナイロン,アクリル,ポリエス
テル等の合成繊維束に、メラミン,エポキシ,フエノー
ル等の熱硬化性樹脂またはポリウレタン等の熱可塑性樹
脂を含浸させ圧縮加熱した成形品が知られている。例え
ば、特公昭42−7165号公報にはメラミン樹脂を使
用した成形品が開示されている。さらに、含浸液を用い
ずそれ自身の一部を加熱溶融して一体化した成形品も知
られている。例えば、特公昭53−47730号公報に
は溶融温度の異なるポリエチレンとポリプロピレンから
なる芯鞘型複合繊維を、ポリエチレンの融点以上、ポリ
プロピレンの融点以下で熱融着させた成形品が開示され
ている。2. Description of the Related Art Conventionally, wool felt has been used for the nib of writing instruments such as felt-tip pens and markers. In addition, recently, molded products are known in which synthetic fiber bundles such as vinylon, nylon, acrylic, and polyester are impregnated with thermosetting resins such as melamine, epoxy, and phenol, or thermoplastic resins such as polyurethane, and then compressed and heated. . For example, Japanese Patent Publication No. 42-7165 discloses a molded article using melamine resin. Furthermore, there are also known molded products that are integrated by heating and melting a part of the product without using an impregnating liquid. For example, Japanese Patent Publication No. 53-47730 discloses a molded article in which core-sheath composite fibers made of polyethylene and polypropylene having different melting temperatures are thermally fused at a temperature above the melting point of polyethylene and below the melting point of polypropylene.
【0003】0003
【発明が解決しようとする課題】しかしながら、上記羊
毛フエルトを用いたものは、羊毛のスケール同士の絡ま
りによつて強力,硬さが付与されているにすぎないため
、繊維がほぐれて崩形しやすいという欠点がある。また
、上記羊毛フエルトを細く切断すると繊維長が短くなつ
てさらに強度が低下するため細い芯ができず、細字用の
製品が得られないという問題もある。[Problem to be Solved by the Invention] However, the above-mentioned wool felts are only given strength and hardness by the intertwining of the wool scales, so the fibers loosen and lose their shape. It has the disadvantage of being easy. In addition, when the above-mentioned wool felt is cut into thin pieces, the fiber length becomes short and the strength further decreases, so that a thin core cannot be formed and a product for fine print cannot be obtained.
【0004】一方、合成繊維束に樹脂を含浸させた成形
品には、樹脂溶液を含浸させたものと樹脂エマルジヨン
液を含浸させたものの二通りがあるが、それぞれ下記の
ような問題を有するため、その改善が求められている。
すなわち、前者の場合は、溶剤が有害な有機溶媒である
ことが多いため、含浸品からこの溶剤を乾燥回収するた
めの装置を設けなければならず、多大な設備投資が必要
となりコスト高を招くという問題がある。また、後者の
場合は、繊維束中にエマルジヨンが点在し、繊維間空隙
がところどころ樹脂で塞がれるようになるため、使用時
にインクのスムーズな流れが妨げられインクかすれを生
じやすいという問題がある。そして、これらのものは、
繊維内に残留する樹脂によつてインクが変質して凝固す
る場合があるという問題もある。On the other hand, there are two types of molded products made by impregnating synthetic fiber bundles with resin: those impregnated with a resin solution and those impregnated with a resin emulsion liquid, but each has the following problems. , improvement is required. In the former case, since the solvent is often a harmful organic solvent, it is necessary to install equipment to dry and recover this solvent from the impregnated product, which requires a large investment in equipment and increases costs. There is a problem. In addition, in the latter case, the emulsion is scattered in the fiber bundle, and the voids between the fibers are filled with resin in places, which prevents the smooth flow of ink during use and tends to cause ink smearing. be. And these things are
There is also the problem that the ink may change in quality and coagulate due to the resin remaining in the fibers.
【0005】さらに、上記芯鞘型複合繊維を熱融着させ
た成形品は、例えばポリエチレン/ポリプロピレン芯鞘
型複合繊維ではポリエチレンとポリプロピレンの融点差
を利用して熱融着させるが、溶融したポリエチレンが液
状となり、表面張力で塊状に融着点に集まるため、この
塊状ポリエチレンが繊維間空隙を塞ぐようなかたちとな
り、上記樹脂エマルジヨンを用いたものと同様の問題が
生じる。Furthermore, molded products made by heat-sealing the above-mentioned core-sheath type composite fibers are, for example, polyethylene/polypropylene core-sheath type composite fibers, which are heat-sealed using the difference in melting point between polyethylene and polypropylene. Since the polyethylene becomes liquid and collects in lumps at the melting point due to surface tension, the lumps of polyethylene close the gaps between the fibers, resulting in the same problems as those using the resin emulsion described above.
【0006】本発明は、このような事情に鑑みなされた
もので、繊維間空隙を塞ぐような夾雑物がなく、均一な
インクの流動性があつて筆記時にインクがかすれるよう
なことのない筆記具用ペン先芯およびそれを安価に製造
する方法の提供をその目的とする。The present invention has been made in view of the above circumstances, and provides a writing instrument that does not contain foreign matter that would block the interfiber spaces, has uniform ink fluidity, and does not cause the ink to become blurred when writing. The purpose of the present invention is to provide a pen nib for use with pens and a method for manufacturing the same at low cost.
【0007】[0007]
【課題を解決するための手段】上記の目的を達成するた
め、本発明は、密度0.15〜0.75に熱融着された
繊維集合体からなる筆記具用ペン先芯であつて、上記繊
維集合体の50重量%以上がアクリル系繊維によつて構
成されている筆記具用ペン先芯を第1の要旨とし、アク
リル系繊維に、アクリル系繊維用溶剤を0.5重量%以
上付着させる工程と、上記溶剤付アクリル系繊維が50
重量%以上均一に混合された繊維束をつくる工程と、上
記繊維束を、200℃以上に保持したガイドを通過させ
ると同時に加圧熱融着させる工程とを備えた筆記具用ペ
ン先芯の製法を第2の要旨とし、アクリル系繊維に、ア
クリル系繊維用溶剤を0.5重量%以上付着させる工程
と、上記溶剤付アクリル系繊維が50重量%以上均一に
混合されたスライバーをつくる工程と、上記スライバー
を、表面温度が200℃以上に設定された口金内を加圧
通過させることにより溶剤付アクリル系繊維を互いに熱
融着させて棒状に成形する工程と、上記棒状体を所定長
さに切断してペン先芯形状に成形する工程とを備えた筆
記具用ペン先芯の製法を第3の要旨とする。[Means for Solving the Problems] In order to achieve the above object, the present invention provides a pen nib core for a writing instrument made of a fiber aggregate heat-sealed to a density of 0.15 to 0.75, which The first aspect is a writing instrument nib core in which 50% by weight or more of the fiber aggregate is composed of acrylic fibers, and 0.5% by weight or more of a solvent for acrylic fibers is attached to the acrylic fibers. process, and the above solvent coated acrylic fiber is 50%
A method for manufacturing a pen nib for a writing instrument, comprising the steps of creating a fiber bundle uniformly mixed at a weight percent or more, and passing the fiber bundle through a guide maintained at 200° C. or higher and simultaneously fusing it under pressure and heat. The second gist is a step of adhering 0.5% by weight or more of a solvent for acrylic fibers to acrylic fibers, and a step of creating a sliver in which 50% by weight or more of the solvent-coated acrylic fibers are uniformly mixed. , a step of forming the sliver into a rod shape by heat-sealing the solvent-coated acrylic fibers to each other by passing the sliver under pressure through a nozzle whose surface temperature is set to 200° C. or higher; and forming the rod-like body into a predetermined length. The third gist is a method for manufacturing a pen nib for a writing instrument, which includes the steps of cutting into pieces and forming the nib into a pen nib shape.
【0008】[0008]
【作用】すなわち、本発明は、アクリル系繊維に溶剤を
付着させ、繊維表面を膨潤させることによつて繊維表面
のみを熱融着できる状態とし、繊維内部は熱融着温度に
よつては溶融しないようにしたものである。したがつて
、この溶剤付アクリル系繊維を熱融着して得られる繊維
集合体は、繊維同士が互いに接した部分で接着され、一
定の強力が確保されているとともに繊維間の空隙も塞が
れるようなことがない。このため、従来の、樹脂エマル
ジヨンを含浸させたものや芯鞘型複合樹脂を用いた場合
のように、使用時にインクかすれを生じることがない。
また、強力も充分に確保されるため、細字用に細く成形
することもできる。[Operation] That is, in the present invention, by attaching a solvent to acrylic fiber and swelling the fiber surface, only the fiber surface can be heat-sealed, and the inside of the fiber may be melted depending on the heat-sealing temperature. I tried not to do that. Therefore, the fiber aggregate obtained by heat-sealing these solvent-coated acrylic fibers is bonded where the fibers touch each other, ensuring a certain level of strength and also sealing the voids between the fibers. There is no chance that I will be disappointed. Therefore, ink smearing does not occur during use, unlike in the case of conventional inks impregnated with resin emulsion or core-sheath type composite resins. In addition, since sufficient strength is ensured, it can be formed into thin shapes for fine characters.
【0009】つぎに、本発明を詳細に説明する。Next, the present invention will be explained in detail.
【0010】本発明に用いるアクリル系繊維としては、
アクリロニトリルのみを単独重合させたポリアクリロニ
トリルからなるアクリル繊維の外、アクリロニトリルを
主要成分としこれに各種の共重合モノマーを配合して得
られる共重合体からなるアクリル系繊維をあげることが
できる。上記共重合モノマーとしては、メチルアクリレ
ート,酢酸ビニル,アクリルアミド,アクリル酸,塩化
ビニル,塩化ビニリデン等が、単独もしくは2種以上の
組み合わせで用いられる。ただし、これらの共重合モノ
マーの使用量は、全体に対し60重量%(以下「%」と
略す)以下に設定することが好適である。また、他の共
重合モノマーとして、アリルスルホン酸ナトリウム,メ
タクリルスルホン酸ナトリウム,2−アクリルアミド2
−メチルプロパンスルホン酸ナトリウム等が、単独もし
くは2種以上の組み合わせで用いられる。そして、これ
らの共重合モノマーの使用量は、全体に対し0.5〜4
%に設定することが好適である。Acrylic fibers used in the present invention include:
In addition to acrylic fibers made of polyacrylonitrile made by homopolymerizing only acrylonitrile, acrylic fibers made of copolymers made of acrylonitrile as a main component and blended with various copolymer monomers can be mentioned. As the copolymerizable monomer, methyl acrylate, vinyl acetate, acrylamide, acrylic acid, vinyl chloride, vinylidene chloride, etc. are used alone or in combination of two or more. However, the amount of these copolymerizable monomers used is preferably set to 60% by weight (hereinafter abbreviated as "%") or less based on the total weight. In addition, other copolymerizable monomers include sodium allylsulfonate, sodium methacrylsulfonate, 2-acrylamide 2
- Sodium methylpropanesulfonate and the like can be used alone or in combination of two or more. The amount of these copolymerized monomers used is 0.5 to 4
It is preferable to set it to %.
【0011】上記モノマーから本発明のアクリル系繊維
を得る方法は、公知のどのような方法によつても差し支
えない。このようなアクリル系繊維としては、市販品で
あるカシミロン(旭化成社製),エクスラン(日本エク
スラン社製),ボンネル(三菱レイヨン),ベスロン(
東邦レーヨン社製),トレロン(東レ社製),カネカロ
ン(鐘淵化学社製)をあげることができる。The acrylic fiber of the present invention can be obtained from the above monomer by any known method. Examples of such acrylic fibers include commercially available products such as Cashmiron (manufactured by Asahi Kasei Co., Ltd.), Exlan (manufactured by Japan Exlan Co., Ltd.), Bonnel (Mitsubishi Rayon), and Veslon (manufactured by Nihon Exlan Co., Ltd.).
(manufactured by Toho Rayon Co., Ltd.), Toleron (manufactured by Toray Industries, Inc.), and Kanekalon (manufactured by Kanekabuchi Chemical Co., Ltd.).
【0012】なお、本発明のアクリル系繊維は、染色後
であつても、原着綿であつてもよい。The acrylic fiber of the present invention may be dyed or spun-dyed cotton.
【0013】また、本発明に用いる溶剤としては、一般
的にアクリル系繊維製造に用いられるアクリルの溶剤を
用いることができる。例えば、ジメチルスルフオキシド
(DMSO),ジメチルアセトアミド(DMA),ジメ
チルフオルムアミド(DMF),スルフオラン(SO)
,エラレンカーボネート(EC)等があげられ、なかで
も、沸点の高いSOが好適である。ただし、これらは単
独で用いても2種以上を併用してもよい。[0013] Furthermore, as the solvent used in the present invention, an acrylic solvent generally used in the production of acrylic fibers can be used. For example, dimethyl sulfoxide (DMSO), dimethylacetamide (DMA), dimethylformamide (DMF), sulforane (SO)
, Elalene carbonate (EC), etc. Among them, SO having a high boiling point is preferred. However, these may be used alone or in combination of two or more.
【0014】本発明では、上記溶剤を、前記アクリル系
繊維に均一付着させる。このとき、付着量は、繊維重量
に対し0.5%以上に設定することが必要で、なかでも
1%以上にすることが好適である。付着量が0.5%未
満では得られる溶剤付アクリル系繊維の熱融着が不充分
となつてペン先芯として成形しにくいからである。なお
、溶剤を付着する方法としては、スプレーで直接溶剤を
繊維表面に噴霧したのち、繊維を充分に混綿する方法も
あるが、この方法では少量の溶剤を均一に全体にゆきわ
たらせるのがむずかしいため、例えば水,アセトン等の
揮発しやすい希釈剤で上記溶剤を希釈し、この希釈液を
アクリル系繊維に均一にスプレーするか、この希釈液中
にアクリル系繊維を浸漬することが好ましい。上記スプ
レー法および浸漬法のいずれかによつて溶剤を繊維表面
に付着させたのち、所定条件で乾燥することにより、希
釈剤を揮散除去し、溶剤によつて繊維表面が膨潤した溶
剤付アクリル系繊維を得ることができる。[0014] In the present invention, the above-mentioned solvent is uniformly adhered to the above-mentioned acrylic fiber. At this time, it is necessary to set the adhesion amount to 0.5% or more based on the fiber weight, and preferably 1% or more. This is because if the amount of adhesion is less than 0.5%, the resulting solvent-coated acrylic fibers will not have sufficient heat fusion and will be difficult to form into a pen tip core. Another way to apply the solvent is to spray the solvent directly onto the fiber surface and then mix the fibers thoroughly, but with this method it is difficult to spread a small amount of solvent evenly over the entire fiber. Therefore, it is preferable to dilute the above-mentioned solvent with an easily volatile diluent such as water or acetone, and spray this diluted solution uniformly onto the acrylic fibers, or immerse the acrylic fibers in this diluted solution. A solvent-coated acrylic product in which the fiber surface is swollen by the solvent, and the diluent is removed by volatilization by attaching the solvent to the fiber surface by either the spray method or the dipping method described above, and then drying under specified conditions. Fiber can be obtained.
【0015】なお、上記溶剤付アクリル系繊維の乾燥温
度は、70℃以下、なかでも60℃以下に設定すること
が好適である。すなわち、乾燥が進行すると繊維表面の
溶剤が繊維表面内側に含浸され繊維表面の膨潤が促され
るが、乾燥温度が高すぎると、繊維同士が接着されてし
まう。特に、80℃を超えると接着が著しくなり好まし
くない。ただし、乾燥によつて多少繊維間が膠着してい
る場合には、混綿前によく開繊すればよい。[0015] The drying temperature of the solvent-coated acrylic fiber is preferably set to 70°C or lower, particularly 60°C or lower. That is, as drying progresses, the solvent on the fiber surface impregnates the inside of the fiber surface, promoting swelling of the fiber surface, but if the drying temperature is too high, the fibers will adhere to each other. In particular, if the temperature exceeds 80°C, adhesion will become significant, which is not preferable. However, if the fibers are somewhat stuck together due to drying, the fibers may be opened thoroughly before blending.
【0016】このようにして得られた溶剤付アクリル系
繊維は、例えばつぎのようにして筆記具用ペン先芯に成
形することができる。すなわち、まず、上記溶剤付アク
リル系繊維を、通常の方法に従つてウエブ化する。この
とき、溶剤付アクリル系繊維のみを用いてもよいし、他
の繊維を混合するようにしてもよい。ただし、溶剤付ア
クリル系繊維が50%以上になるよう設定する必要があ
り、より強力なものを得ようとすれば、溶剤付アクリル
系繊維の配合割合を多くすればよい。逆に、溶剤付アク
リル系繊維が50%未満では得られる成形品の強力が不
充分となつて商品としても品質を得ることができない。The solvent-coated acrylic fiber thus obtained can be formed into a nib core for a writing instrument, for example, in the following manner. That is, first, the solvent-coated acrylic fibers are formed into a web according to a conventional method. At this time, only the solvent-coated acrylic fibers may be used, or other fibers may be mixed. However, it is necessary to set the amount of solvent-coated acrylic fibers to 50% or more, and if you want to obtain a stronger product, you can increase the blending ratio of solvent-coated acrylic fibers. On the other hand, if the solvent-coated acrylic fiber is less than 50%, the resulting molded product will not have sufficient strength and will not be of good quality as a product.
【0017】得られたウエブは、通常の熱カレンダーに
かけることにより熱処理し熱融着させて不織布にする。
この不織布の接着力は、上記熱カレンダーの表面温度,
加重圧力,ウエブの厚み,目付,ウエブの通過時間等で
異なるが、例えば150g/m2 の目付のウエブを熱
カレンダー表面温度200℃,ローラー加重10kgゲ
ージで熱処理する場合、上記溶剤付アクリル系繊維の混
合率を50%以上に設定する必要がある。さらに、接着
力の強い不織布を得ようとすれば、溶剤付アクリル系繊
維の混合率を大きくすればよい。なお、混合率が75%
未満では、ウエブの通過時間を長くするとともに、熱カ
レンダーの加重圧力を高くすることが好ましい。また、
硬度の高いペン先芯が必要な場合には、熱カレンダー表
面温度を230℃以上にすることが好ましい。このよう
にして得られた不織布を、型枠に合わせてプレスで打ち
抜いて筆記具用ペン先芯を作製することができる。[0017] The obtained web is subjected to a heat treatment by applying it to a conventional thermal calender and is thermally fused to form a non-woven fabric. The adhesive strength of this nonwoven fabric is determined by the surface temperature of the thermal calendar,
Although it varies depending on the applied pressure, web thickness, fabric weight, web passing time, etc., for example, when a web with a fabric weight of 150 g/m2 is heat-treated with a thermal calendar surface temperature of 200°C and a roller weight of 10 kg gauge, the above-mentioned solvent-coated acrylic fibers It is necessary to set the mixing ratio to 50% or more. Furthermore, in order to obtain a nonwoven fabric with strong adhesive strength, the mixing ratio of solvent-coated acrylic fibers may be increased. In addition, the mixing ratio is 75%
If it is less than 100%, it is preferable to lengthen the passage time of the web and increase the applied pressure of the thermal calendar. Also,
When a pen nib with high hardness is required, it is preferable to set the thermal calendar surface temperature to 230° C. or higher. The nonwoven fabric thus obtained can be punched out using a press in accordance with a mold to produce a nib core for a writing instrument.
【0018】また、上記のように不織布を経由してペン
先芯に成形するのではなく、スライバーからペン先芯を
成形することもできる。この場合には、溶剤付アクリル
系繊維のみ、あるいは溶剤付アクリル系繊維と他の繊維
とを均一に混綿したものを用い、通常の方法に従つてス
ライバーをつくる。そして、このスライバーを、加熱し
た口金を加圧通過させることによりペン先芯を得ること
ができる。なお、上記口金の表面温度は、200℃以上
、なかでも硬度の高いペン先芯を得ようとすれば230
℃以上に設定することが好適である。Furthermore, instead of forming the nib core through a nonwoven fabric as described above, the nib core can also be formed from a sliver. In this case, a sliver is made using only solvent-coated acrylic fibers or a uniform mixture of solvent-coated acrylic fibers and other fibers according to a conventional method. Then, by passing this sliver through a heated cap under pressure, a pen tip core can be obtained. In addition, the surface temperature of the above-mentioned cap should be 200°C or higher, especially 230°C if you want to obtain a pen tip with high hardness.
It is preferable to set the temperature to ℃ or higher.
【0019】なお、上記不織布を経由する方法およびス
ライバーを経由する方法のいずれについても、ペン先芯
の密度を0.15〜0.75に設定することが必要で、
なかでも0.2〜0.7にすることが好適である。すな
わち、密度が0.15未満では、ペン先芯の強力,硬さ
が不足する上、インクの保持力が不足し、ペン先を上に
向けるとインクかすれの原因となる。逆に、密度が0.
75を超えると、ペン先芯の繊維間空隙が少なくなり、
インクの流動性が阻害されてインクかすれの原因となる
。[0019] For both the method using the nonwoven fabric and the method using the sliver, it is necessary to set the density of the pen tip core to 0.15 to 0.75.
Among these, it is preferable to set it to 0.2 to 0.7. That is, if the density is less than 0.15, the strength and hardness of the nib core will be insufficient, and the ink holding power will be insufficient, causing ink to fade when the nib is turned upward. Conversely, if the density is 0.
When it exceeds 75, the inter-fiber voids in the pen tip core decrease,
This impedes the fluidity of the ink and causes ink to fade.
【0020】このようにして得られた筆記具用ペン先芯
は、繊維間に夾雑物がなく、インクの流動性がよいため
、筆記時にインクがかすれるようなことがない。また、
用途,形状に応じて適当な強力と硬さを保持することが
できる。[0020] The pen nib for writing instruments thus obtained has no impurities between the fibers and the ink has good fluidity, so the ink does not smudge when writing. Also,
Appropriate strength and hardness can be maintained depending on the application and shape.
【0021】つぎに、実施例について比較例と併せて示
す。Next, examples will be shown together with comparative examples.
【0022】[0022]
【実施例1〜3、比較例1】市販のカネボウアクリルR
K1BR3dx102mm(鐘紡社製)を原料アクリル
系繊維として使用した。このアクリル系繊維10gを1
00mlの溶剤水溶液に、後記の表1に示す条件で浸漬
処理した。この処理品の熱融着強力について評価し、下
記の表1に併せて示す。[Examples 1 to 3, Comparative Example 1] Commercially available Kanebo Acrylic R
K1BR3dx102mm (manufactured by Kanebo Co., Ltd.) was used as the raw material acrylic fiber. 10g of this acrylic fiber
The sample was immersed in 00 ml of an aqueous solvent solution under the conditions shown in Table 1 below. The heat fusion strength of this treated product was evaluated and is also shown in Table 1 below.
【0023】[0023]
【表1】[Table 1]
【0024】[0024]
【実施例4〜7】上記実施例1と同様の条件で溶剤付着
を行い(SOが3.8%付着)、遠心脱水機で絞つたの
ち下記の表2に示す条件で熱風乾燥機で乾燥した。この
ようにして得られた溶剤付アクリル繊維を開繊し、開繊
に支障が生じるか否かを評価した。この結果を下記の表
2に併せて示す。[Examples 4 to 7] Solvent deposition was carried out under the same conditions as in Example 1 above (3.8% SO attached), squeezed with a centrifugal dehydrator, and then dried with a hot air dryer under the conditions shown in Table 2 below. did. The solvent-coated acrylic fibers thus obtained were opened, and it was evaluated whether or not there would be any trouble in opening the fibers. The results are also shown in Table 2 below.
【0025】[0025]
【表2】[Table 2]
【0026】[0026]
【実施例8〜11、比較例2,3】上記実施例1と同様
の条件で溶剤付着を行い(SOが3.8%付着)、乾燥
条件60℃×120分で乾燥することにより得られた溶
剤付アクリル繊維を、80%の混合率で通常のアクリル
と混打綿機でミツクスし、カーデイング後、練条を3回
掛け、所定のゲレンとなるようゲレンを変更して下記の
表3に示すように得られるペン先芯の密度を調整した。
つぎに、このウエブを、内径5mmの口金(表面温度2
30℃)内を通過させて熱処理を行い棒状に加工した。
そして、所定の長さに切断し、片端部を研磨して筆記具
用ペン先芯を作製した。このようにして得られたペン先
芯を用いて筆記具を製造し、使用によつてインクかすれ
が生じるか否かを評価した。この結果を下記の表3に併
せて示す。[Examples 8 to 11, Comparative Examples 2 and 3] Solvent deposition was carried out under the same conditions as in Example 1 (3.8% SO was attached), and drying was performed at 60°C for 120 minutes. The solvent-coated acrylic fibers were mixed with normal acrylic at a mixing rate of 80% using a cotton mixing machine, and after carding, they were drawn three times and the gel was changed to obtain the desired gel, as shown in Table 3 below. The density of the resulting pen nib was adjusted as shown in . Next, this web was attached to a mouthpiece with an inner diameter of 5 mm (surface temperature 2
The material was heat-treated by passing through a temperature of 30° C.) and processed into a rod shape. Then, it was cut into a predetermined length and one end was polished to produce a nib core for a writing instrument. A writing instrument was manufactured using the pen nib obtained in this way, and it was evaluated whether or not the ink would fade with use. The results are also shown in Table 3 below.
【0027】[0027]
【表3】[Table 3]
【0028】[0028]
【実施例12,13、比較例4】また、溶剤付アクリル
系繊維の混合率を下記の表4に示すように変え、それ以
外の処理条件は上記実施例8と同様にして筆記具用ペン
先芯を得た。そして、これらのペン先芯の圧縮強力を測
定した。この結果を下記の表4に併せて示す。[Examples 12 and 13, Comparative Example 4] In addition, the mixing ratio of the solvent-coated acrylic fiber was changed as shown in Table 4 below, and the other processing conditions were the same as in Example 8 above. I got the core. Then, the compressive strength of these pen nib cores was measured. The results are also shown in Table 4 below.
【0029】[0029]
【表4】[Table 4]
【0030】[0030]
【発明の効果】以上のように、本発明の筆記具用ペン先
芯は、繊維間空隙に夾雑物がなく、バインダーとしての
樹脂を使用しないため、インクが残留樹脂によつて変質
することもない。したがつて、インクの流動性が妨げら
れることがなく、筆記時にインクかすれを生じにくい。
また、用途,形状に応じて適当な強力と硬さを確保する
ことができる。さらに、本発明の方法によれば、溶剤回
収工程が不要であり、生産効率よく、安価に上記筆記具
用ペン先芯を製造することができる。[Effects of the Invention] As described above, the writing instrument nib core of the present invention has no impurities in the interfiber spaces and does not use resin as a binder, so the ink does not deteriorate due to residual resin. . Therefore, the fluidity of the ink is not hindered, and ink smearing is less likely to occur when writing. In addition, appropriate strength and hardness can be ensured depending on the application and shape. Further, according to the method of the present invention, there is no need for a solvent recovery step, and the writing instrument nib core can be manufactured with high production efficiency and at low cost.
Claims (3)
た繊維集合体からなる筆記具用ペン先芯であつて、上記
繊維集合体の50重量%以上がアクリル系繊維によつて
構成されていることを特徴とする筆記具用ペン先芯。1. A writing instrument nib core made of a fiber aggregate heat-sealed to a density of 0.15 to 0.75, wherein 50% by weight or more of the fiber aggregate is composed of acrylic fibers. A writing instrument pen nib characterized by:
溶剤を0.5重量%以上付着させる工程と、上記溶剤付
アクリル系繊維が50重量%以上均一に混合された繊維
束をつくる工程と、上記繊維束を、200℃以上に保持
したガイドを通過させると同時に加圧熱融着させる工程
とを備えたことを特徴とする筆記具用ペン先芯の製法。2. A step of attaching 0.5% by weight or more of a solvent for acrylic fibers to acrylic fibers, and a step of creating a fiber bundle in which 50% by weight or more of the solvent-coated acrylic fibers are uniformly mixed. A method for producing a nib core for a writing instrument, comprising the step of passing the fiber bundle through a guide maintained at 200° C. or higher and simultaneously pressurizing and heat-sealing the fiber bundle.
溶剤を0.5重量%以上付着させる工程と、上記溶剤付
アクリル系繊維が50重量%以上均一に混合されたスラ
イバーをつくる工程と、上記スライバーを、表面温度が
200℃以上に設定された口金内を加圧通過させること
により溶剤付アクリル系繊維を互いに熱融着させて棒状
に成形する工程と、上記棒状体を所定長さに切断してペ
ン先芯形状に成形する工程とを備えたことを特徴とする
筆記具用ペン先芯の製法。3. A step of adhering 0.5% by weight or more of an acrylic fiber solvent to the acrylic fiber, a step of producing a sliver in which 50% by weight or more of the solvent-coated acrylic fiber is uniformly mixed; The sliver is passed under pressure through a nozzle whose surface temperature is set to 200°C or higher to heat-fuse the solvent-coated acrylic fibers to each other to form a rod shape, and the rod-shaped body is cut into a predetermined length. A method for manufacturing a pen nib for a writing instrument, comprising the step of: forming the nib into a pen nib shape.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3157667A JPH04355196A (en) | 1991-05-31 | 1991-05-31 | Pen point lead for writing utensils and production thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3157667A JPH04355196A (en) | 1991-05-31 | 1991-05-31 | Pen point lead for writing utensils and production thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH04355196A true JPH04355196A (en) | 1992-12-09 |
Family
ID=15654752
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3157667A Pending JPH04355196A (en) | 1991-05-31 | 1991-05-31 | Pen point lead for writing utensils and production thereof |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH04355196A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005035278A (en) * | 2003-06-24 | 2005-02-10 | Aubex Corp | Fiber nib and manufacturing method thereof |
-
1991
- 1991-05-31 JP JP3157667A patent/JPH04355196A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005035278A (en) * | 2003-06-24 | 2005-02-10 | Aubex Corp | Fiber nib and manufacturing method thereof |
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