JPS5840595B2 - Enpitsu Shin no Seizou Hohou - Google Patents
Enpitsu Shin no Seizou HohouInfo
- Publication number
- JPS5840595B2 JPS5840595B2 JP7529075A JP7529075A JPS5840595B2 JP S5840595 B2 JPS5840595 B2 JP S5840595B2 JP 7529075 A JP7529075 A JP 7529075A JP 7529075 A JP7529075 A JP 7529075A JP S5840595 B2 JPS5840595 B2 JP S5840595B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- core
- hohou
- enpitsu
- seizou
- 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
- Inks, Pencil-Leads, Or Crayons (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
【発明の詳細な説明】
本発明は鉛筆芯の製造方法に関するもので、詳しくはバ
インダーとして架橋結合可能な樹脂を用い、所望の硬度
の鉛筆芯を任意に得る方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a pencil lead, and more particularly to a method for obtaining a pencil lead having a desired hardness by using a crosslinkable resin as a binder.
従来、鉛筆芯の製造方法は粘土をバインダーとしたもの
があるが、粘結力が小さく曲げ強度も弱く、耐摩耗等の
諸性能が十分に得られない欠点があった。Conventionally, pencil leads have been produced using clay as a binder, but these have had the drawbacks of low cohesive strength, low bending strength, and insufficient performance such as abrasion resistance.
又、1000℃付近で焼成するため焼成設備、熱源の確
保の点から経済的にも不利であった。Furthermore, since firing is performed at around 1000° C., it is economically disadvantageous in terms of securing firing equipment and heat sources.
又、粘土を使用しない方法として高分子物質をバインダ
ーとして用い焼成(熱分解)する方法があるが、焼成条
件の調整が難しく品質の維持管理は大変であり、熱源の
点からも経済的に不利であった。Another method that does not use clay is to use a polymeric substance as a binder and fire it (pyrolyze it), but it is difficult to adjust the firing conditions and quality maintenance is difficult, and it is economically disadvantageous in terms of the heat source. Met.
又、特公昭49−12302号公報では黒鉛と熱可塑性
樹脂から芯を成形する方法が述べられているが、この方
法で硬度の相異する所望の芯を得るには困難であり、強
度を上げるには熱可塑性樹脂の量を多くしなければなら
ないので筆記時の書き味が悪くなる欠点が生ずる。Furthermore, Japanese Patent Publication No. 49-12302 describes a method of molding a core from graphite and a thermoplastic resin, but it is difficult to obtain cores with desired hardnesses using this method, and it is difficult to obtain cores with different hardnesses using this method. Since it is necessary to use a large amount of thermoplastic resin, the disadvantage is that the writing quality becomes poor.
本発明は、前述の問題点を解決する方法について種々研
究した結果、架橋結合を起こさせる樹脂を種々選択し、
その架橋の度合いにより折損強度、摩耗等の諸性能を良
好に維持しながら所望の硬度の鉛筆芯が得られる点に着
目し、本発明を完成するに到った。As a result of various studies on methods for solving the above-mentioned problems, the present invention has been made by selecting various resins that cause crosslinking,
The present invention was completed based on the fact that depending on the degree of crosslinking, a pencil lead having a desired hardness can be obtained while maintaining various properties such as breakage strength and abrasion.
本発明の方法は、黒鉛およびカーボンブラックとポリ塩
化ビニール樹脂、又はその共重合樹脂に酸化亜鉛、酸化
アンチモン、メルカプトイミダシリンより選ばれた1種
又は2種以上と配合した組成物を混線、加熱、成形して
架橋させてなる鉛筆を製造することからなっている。The method of the present invention involves mixing a composition in which graphite and carbon black are blended with a polyvinyl chloride resin or a copolymer resin thereof with one or more selected from zinc oxide, antimony oxide, and mercaptoimidacillin. It consists of producing pencils by heating, molding, and crosslinking.
すなわち、本発明に使用する樹脂はポリ塩化ビニール樹
脂、又はその共重合樹脂である。That is, the resin used in the present invention is a polyvinyl chloride resin or a copolymer resin thereof.
共重合樹脂としては酢酸ビニール、エチレン、プロピレ
ン、などと共重合した樹脂が有用である。As the copolymer resin, resins copolymerized with vinyl acetate, ethylene, propylene, etc. are useful.
ポリ塩化ビニール系樹脂は約120℃以上の加熱により
脱塩酸することは公知であり、約300℃で脱塩酸が完
全に終了することも知られている。It is known that polyvinyl chloride resin is dehydrochlorinated by heating at about 120°C or higher, and it is also known that dehydrochlorination is completely completed at about 300°C.
この状態では鉛筆芯として強度が得られず実用的には特
公昭37−1970で述べられているように1000℃
位の高温にて処理し炭化させることが必要である。In this state, it is not strong enough to be used as a pencil lead, and for practical purposes, as stated in the Japanese Patent Publication No. 37-1970, 1000℃ is required.
It is necessary to process and carbonize at a high temperature of about 100 ml.
本発明者等は鋭意努力の結果、200℃迄の温度で橋か
け剤を添加して樹脂を架橋させ強度の向上をはかり、実
用的に可能とした。As a result of diligent efforts, the present inventors added a crosslinking agent at a temperature of up to 200°C to crosslink the resin, aiming to improve the strength, and made it practical.
例えば、
なる架橋反応を生じると推定され、非常に強度のある反
応物が得られる。For example, it is estimated that the following crosslinking reaction occurs, and a very strong reaction product is obtained.
この反応物はいかなる溶剤にも溶解せず安定した物質で
ある。This reactant is a stable substance that does not dissolve in any solvent.
したがって、使用する樹脂の重合度、共重合率、橋かけ
剤の量により、各種の硬度の異なった鉛筆芯を自由に製
造することが出来る。Therefore, pencil leads having various hardnesses can be freely produced depending on the degree of polymerization of the resin used, the copolymerization rate, and the amount of crosslinking agent.
本発明における鉛筆芯の製造は、ポリ塩化ビニール樹脂
又はその共重合樹脂を溶剤にて高速ミキサーを用いて充
分溶解し、後黒鉛、カーボン、橋かけ剤、必要によって
体質、可塑剤、脂肪醜行ケン等を添加し、三本ロールで
冷却しながら練合し、溶剤を大部分蒸発させ、棒状に成
形し加熱押出成形する。The production of the pencil lead in the present invention involves sufficiently dissolving polyvinyl chloride resin or its copolymer resin in a solvent using a high-speed mixer, and then adding graphite, carbon, a crosslinking agent, if necessary, a physical constitution, a plasticizer, a fat and oxidation binder, etc. etc., are kneaded with three rolls while cooling, most of the solvent is evaporated, and the mixture is formed into a rod shape and heated and extruded.
この製造法における芯中の樹脂の含有率は20多以下が
良好で、これ以上増加すると書き味が悪くなる結果を得
る。In this manufacturing method, the content of resin in the core is preferably 20 or less, and if it increases more than this, the writing quality becomes poor.
以下に実施例を示す。Examples are shown below.
実施例 1
黒 鉛 40.0重量部カー
ボンブラック 5.O〃ステアリン酸
マグネシウム 18.0//酸化亜鉛
1.5〃塩ビ一酢ビ共重合樹脂
12.0//(ビニール#1000AS重合度3
201塩ビ86%、酢ビ14% 電気化学工業社製)メ
チルエチルケトン 50.Ottメチルエ
チルケトンに先ず樹脂を添加し高速ミキサーで完全に溶
解し、その他のものを順次添加し、三本ロールで冷却し
ながら練合し、溶剤を大部分蒸発させ、棒状に成形し、
これを押出機に充填し180℃にて芯を押出し成形し、
連続した直径2Xの芯を得、これを定尺に切断した。Example 1 Graphite 40.0 parts by weight Carbon black 5. O〃Magnesium stearate 18.0//Zinc oxide
1.5 PVC-vinyl acetate copolymer resin
12.0//(vinyl #1000AS polymerization degree 3
201 86% PVC, 14% PVC (manufactured by Denki Kagaku Kogyo Co., Ltd.) Methyl ethyl ketone 50. First, add the resin to Ott methyl ethyl ketone and completely dissolve it with a high-speed mixer, then add the other ingredients one after another, knead with three rolls while cooling, evaporate most of the solvent, and form it into a rod shape.
Fill this into an extruder and extrude the core at 180°C.
A continuous core with a diameter of 2X was obtained and cut into regular lengths.
得られた芯は硬度HBで、曲げ強度は20,00.0
、!i’ 7m1(JIS6005−1971)、摩擦
係数は0.20で共に優れ、運筆も極めてなめらかであ
った。The obtained core has a hardness of HB and a bending strength of 20,00.0
,! i' 7m1 (JIS6005-1971), the coefficient of friction was 0.20, both excellent, and the writing was extremely smooth.
又、出来た芯をメチルエチルケトン中に添加し、溶解試
験を行った結果、不溶化していることから樹脂は架橋し
ていることを確認した。In addition, the resulting core was added to methyl ethyl ketone and a dissolution test was conducted. As a result, it was found that the core was insolubilized, which confirmed that the resin was crosslinked.
なお、実施例から酸化亜鉛を除いた配合で出来た芯は、
メチルエチルケトンの溶解試験の結果ではよく溶解し、
又その曲げ強度は13,000 g /mAであり、酸
化亜鉛で架橋したものより弱かった。In addition, the core made from the formulation excluding zinc oxide from the example,
The results of the dissolution test of methyl ethyl ketone show that it dissolves well.
Moreover, its bending strength was 13,000 g/mA, which was lower than that crosslinked with zinc oxide.
実施例 2
黒 鉛 35.0重量部カー
ボンブラック 5.o〃ステアリン酸
マグネシウム 16.O//酸化アンチモン
6.o〃ジオクチルスタレート
10.0//塩化ビニール樹脂
13.O//(SH−250重合度2500電気化学
工業社製)
メチルエチルケトン 50.0 //上
記組成物を実施例1と同じように混練操作し、溶剤を大
部分蒸発させ、押出し機に充填し200℃にて芯を押出
処形し、連続した直径2Xの芯を得これを定尺に切断し
た。Example 2 Graphite 35.0 parts by weight Carbon black 5. o Magnesium stearate 16. O//antimony oxide
6. o Dioctyl stalate
10.0//vinyl chloride resin
13. O // (SH-250 degree of polymerization 2500, manufactured by Denki Kagaku Kogyo Co., Ltd.) Methyl ethyl ketone 50.0 // The above composition was kneaded in the same manner as in Example 1, most of the solvent was evaporated, and the extruder was filled with 200 The core was extruded at 0.degree. C. to obtain a continuous core with a diameter of 2X, which was cut to length.
得られた芯は硬度2Hで曲げ強度は21,500 g
/maで、摩擦係数は0.19で共に優れ、運筆も極め
てなめらかであった。The resulting core has a hardness of 2H and a bending strength of 21,500 g.
/ma, the friction coefficient was excellent at 0.19, and the writing was extremely smooth.
又、実施例1と同じように溶解試験の結果、樹脂は不溶
化していることから架橋していることを確認した。Further, as in Example 1, the results of the dissolution test revealed that the resin was insolubilized, which confirmed that it was crosslinked.
なお、実施例から酸化アンチモンを除いた架橋反応を起
こさない配合では、曲げ強度は12,500 g/m4
で弱かった。In addition, in a formulation that does not cause a crosslinking reaction by excluding antimony oxide from the example, the bending strength is 12,500 g/m4
So it was weak.
実施例 3
黒 鉛
カーボンブラック
ステアリン酸マグネシウム
2−メルカプトイミダシリン
エチレン−塩ビ共重合樹脂
(Z−550重合度550
ジオクチルスタレート
メチルエチルケトン
酸化アンチモン
50.0重量部
5、Q tt
18.0tt
1.5〃
12.0//
日量化学社製)
8.0〃
50.0 〃
0.5〃
上記組成物を実施例1と同じように混練操作し、溶剤を
大部分蒸発させ押出し機に充填し、200℃にて芯を押
出し底形し連続した2駕の芯を得、これを定尺に切断し
た。Example 3 Graphite carbon black Magnesium stearate 2-mercaptoimidacillin Ethylene-vinyl chloride copolymer resin (Z-550 Degree of polymerization 550 Dioctyl stalate Methyl ethyl ketone Antimony oxide 50.0 parts by weight 5, Q tt 18.0 tt 1.5 〃 12.0// Manufactured by Nichiryo Kagaku Co., Ltd.) 8.0 〃 50.0 〃 0.5〃 The above composition was kneaded in the same manner as in Example 1, most of the solvent was evaporated, and the mixture was filled into an extruder. The core was extruded at 200° C. to form a bottom shape to obtain two continuous cores, which were cut into regular lengths.
得られた芯は硬度2Bで曲げ強度は20,000 jj
/miで、摩擦係数は0.21で共に優れ、運筆も極
めてなめらかであった。The obtained core has a hardness of 2B and a bending strength of 20,000 jj
/mi, the friction coefficient was 0.21, which was excellent, and the writing was extremely smooth.
又、実施例1と同じように溶解試験の結果、樹脂は不溶
化していることから架橋していることを確認した。Further, as in Example 1, the results of the dissolution test revealed that the resin was insolubilized, which confirmed that it was crosslinked.
なお、実施例から2−メルカプトイミダプリンと酸化ア
ンチモンを除いた架橋反応を起こさない配合では、曲げ
強度は10.00(1/maで弱かった。In addition, in the formulation in which 2-mercaptoimidapurine and antimony oxide were removed from the examples and did not cause a crosslinking reaction, the bending strength was weak at 10.00 (1/ma).
以上の実施例からも明白のごとく、本発明は高分子鎖中
の塩素を低温加熱により脱塩素反応起こし、橋かけ剤を
添加して樹脂を架橋させることにより、硬度の異なる芯
を得ることが出来、しかも折損強度、耐摩耗性も十分満
足するものが得られた。As is clear from the above examples, the present invention makes it possible to obtain cores with different hardness by causing a dechlorination reaction of chlorine in the polymer chain by heating at a low temperature, and by adding a crosslinking agent to crosslink the resin. In addition, a product with sufficiently satisfactory breaking strength and abrasion resistance was obtained.
しかも運筆性も良く、実用上優れたものであった。Moreover, it had good penability and was excellent in practical use.
又本発明は連続生産を可能とし、生産性の向上、コスト
低減に大きく寄与できるものである。Furthermore, the present invention enables continuous production and can greatly contribute to improving productivity and reducing costs.
Claims (1)
脂又はその共重合樹脂に酸化亜鉛、酸化アンチモン、メ
ルカプトイミダシリンより選ばれた1種又は2種以上と
配合した組成物とを、混練加熱成形して架橋結合させる
ことを特徴とする鉛筆芯の製造方法。1. Graphite and carbon black, and a composition in which polyvinyl chloride resin or its copolymer resin is blended with one or more selected from zinc oxide, antimony oxide, and mercaptoimidacillin are kneaded and heated. A method for producing a pencil lead characterized by crosslinking.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7529075A JPS5840595B2 (en) | 1975-06-20 | 1975-06-20 | Enpitsu Shin no Seizou Hohou |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7529075A JPS5840595B2 (en) | 1975-06-20 | 1975-06-20 | Enpitsu Shin no Seizou Hohou |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS52526A JPS52526A (en) | 1977-01-05 |
| JPS5840595B2 true JPS5840595B2 (en) | 1983-09-06 |
Family
ID=13571947
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7529075A Expired JPS5840595B2 (en) | 1975-06-20 | 1975-06-20 | Enpitsu Shin no Seizou Hohou |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5840595B2 (en) |
-
1975
- 1975-06-20 JP JP7529075A patent/JPS5840595B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS52526A (en) | 1977-01-05 |
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