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JP2900622B2 - Manufacturing method of pencil lead - Google Patents
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JP2900622B2 - Manufacturing method of pencil lead - Google Patents

Manufacturing method of pencil lead

Info

Publication number
JP2900622B2
JP2900622B2 JP4725991A JP4725991A JP2900622B2 JP 2900622 B2 JP2900622 B2 JP 2900622B2 JP 4725991 A JP4725991 A JP 4725991A JP 4725991 A JP4725991 A JP 4725991A JP 2900622 B2 JP2900622 B2 JP 2900622B2
Authority
JP
Japan
Prior art keywords
pencil lead
weight
acid
parts
kneading
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 - Lifetime
Application number
JP4725991A
Other languages
Japanese (ja)
Other versions
JPH04252281A (en
Inventor
雄一 宮原
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pentel Co Ltd
Original Assignee
Pentel Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Pentel Co Ltd filed Critical Pentel Co Ltd
Priority to JP4725991A priority Critical patent/JP2900622B2/en
Publication of JPH04252281A publication Critical patent/JPH04252281A/en
Application granted granted Critical
Publication of JP2900622B2 publication Critical patent/JP2900622B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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  • Inks, Pencil-Leads, Or Crayons (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】有機結合材と体質材とを少なくと
も主材とする材料を、混練、成形後、焼成処理を施して
なる鉛筆芯の製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for manufacturing a pencil lead obtained by kneading, shaping, and firing a material containing at least an organic binder and a body material.

【0002】[0002]

【従来の技術】上記した鉛筆芯は一般に有機焼成芯と呼
ばれ、通常、ポリ塩化ビニル系樹脂、ポリビニルアルコ
−ル、フラン樹脂といった有機結合材と、黒鉛、窒化硼
素といった体質材を主材とし、可塑剤、溶剤、安定剤な
どを必要に応じて併用し、これら配合した材料を、ニ−
ダ−、3本ロ−ルといった混練機などで均一分散し、適
宜寸法に成形し、焼成処理を施して炭素骨格を有する焼
成芯体を得、更に、必要に応じてシリコン油、スピンド
ル油、流動パラフィン、モンタンワックス、マイクロク
リスタリンワックスといった適宜油状物質を含浸して得
られている。
2. Description of the Related Art The above-mentioned pencil lead is generally called an organic fired lead, and usually comprises an organic binder such as polyvinyl chloride resin, polyvinyl alcohol and furan resin, and a body material such as graphite and boron nitride. , A plasticizer, a solvent, a stabilizer, and the like, if necessary.
The mixture is uniformly dispersed with a kneader such as a kneader or a three-roll mill, formed into appropriate dimensions, and subjected to a baking treatment to obtain a calcined core having a carbon skeleton. Further, if necessary, silicon oil, spindle oil, It is obtained by appropriately impregnating oily substances such as liquid paraffin, montan wax and microcrystalline wax.

【0003】有機焼成芯は、粘土を結合材として使用す
るいわゆる粘土焼結芯や高温熱処理を施すことなく製造
されるいわゆる生芯タイプのものに比べ、強度の高いも
のになるという長所があり、シャ−プペンシル用芯など
細径のものとして使用されているだけでなく、近年は、
木軸鉛筆の芯のような太径のものとしても使用されるよ
うになってきている。
[0003] The organic fired core has an advantage that it has higher strength than a so-called clay sintered core using clay as a binder or a so-called raw core type manufactured without performing high-temperature heat treatment. In addition to being used as a small diameter such as a sharp pencil lead, in recent years,
It has also come to be used as a large-diameter material such as a wooden pencil lead.

【0004】とは言え、まだまだ欠点があり、より強度
の高いものに、より濃度の濃いものにといった検討が種
々加えられている。例えば、特公昭51−26849号
公報には、気孔の人為的形成手段の一つとして解重合に
より気孔を形成するものの使用についての開示がある
が、概して、気孔形成材を使用すると濃度を向上するこ
とができる。
Nevertheless, there are still some drawbacks, and various studies have been made on higher strength ones and higher density ones. For example, Japanese Patent Publication No. 51-26849 discloses the use of a material that forms pores by depolymerization as one of means for artificially forming pores, but generally, the use of a pore-forming material improves the concentration. be able to.

【0005】[0005]

【発明が解決しようとする課題】上記した気孔形成材の
使用だけではないが、一般に、濃度向上は強度低下を招
き、強度向上は濃度低下を招いてしまう。即ち、濃度と
強度とは逆相関の関係にあり、この関係自体の改善を可
能としたものは意外と少ない。
The use of the above-mentioned pore-forming material is not limited to the use of the above-mentioned pore-forming material, but generally, an increase in the concentration results in a decrease in strength, and an increase in the strength results in a decrease in concentration. That is, there is an inverse correlation between the concentration and the intensity, and there are surprisingly few such relationships that can be improved.

【0006】そこで、本発明は、この濃度−強度の逆相
関関係を改善する一つの方法を提供することを目的とす
る。
Therefore, an object of the present invention is to provide a method for improving the inverse correlation between the concentration and the intensity.

【0007】[0007]

【課題を解決するための手段】材料の一つとして、直鎖
脂肪酸と多価アルコ−ルとのエステル化合物を使用す
る。即ち、本発明は、有機結合材と体質材とを少なくと
も主材とする材料を、混練、成形後、焼成処理を施して
なる鉛筆芯の製造方法において、前記材料の一つとし
て、直鎖脂肪酸と多価アルコ−ルとのエステル化合物を
使用することを特徴とする鉛筆芯の製造方法を要旨とす
る。
Means for Solving the Problems As one of the materials, an ester compound of a linear fatty acid and a polyhydric alcohol is used. That is, the present invention relates to a method for producing a pencil lead obtained by kneading, molding, and baking a material containing at least an organic binder and a constitutional material as main materials, wherein one of the materials is a linear fatty acid. A method for producing a pencil lead, characterized by using an ester compound of phenol and a polyhydric alcohol.

【0008】本発明で使用するエステル化合物として
は、直鎖脂肪酸として、カプリル酸、カプリン酸、ラウ
リン酸、ミリスチン酸、パルミチン酸、ステアリン酸、
1.2ヒドロキシステアリン酸、オレイン酸、リシノレ
イン酸、ベヘニン酸、ヤシ油脂肪酸、エルカ酸、牛脂脂
肪酸、また、多価アルコ−ルとして、エチレングリコ−
ル、ジエチレングリコ−ル、トリエチレングリコ−ル、
ポリエチレングリコ−ル、プロピレングリコ−ル、ネオ
ペンチルグリコ−ル、トリメチロ−ルプロパン、グリセ
リン、ペンタエリスリト−ル、ジペンタエリスリト−ル
の適宜組み合わせによるものなどが例示できる。特に好
ましいのは、常温で液体のものや、加熱下で混練し得る
場合には混練時の温度で液体となるものであり、また、
引火点や煙点が高くて炭素残渣をなるべく残さないもの
である。
The ester compounds used in the present invention include, as straight-chain fatty acids, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid,
1.2 Hydroxystearic acid, oleic acid, ricinoleic acid, behenic acid, coconut oil fatty acid, erucic acid, tallow fatty acid, and polyhydric alcohols such as ethylene glycol
, Diethylene glycol, triethylene glycol,
Examples thereof include those obtained by appropriately combining polyethylene glycol, propylene glycol, neopentyl glycol, trimethylolpropane, glycerin, pentaerythritol, and dipentaerythritol. Particularly preferred are those that are liquid at room temperature and those that become liquid at the temperature at the time of kneading when kneading is possible under heating,
It has a high flash point and smoke point and leaves as little carbon residue as possible.

【0009】ここで、エステル化合物は種々市販されて
おり、一例を挙げると、ヘンケル白水(株)のエデノア
NPG05、同PDO、同PTO、同PEC4、同PE
S、同PGDO、同PMO、同PPE、同TMNC、同
TMP05、同TMPC、同TMTC、同TDO、同T
TO、勝田化工(株)のW−212J、VS−22、A
PLO−200、PU−300PL、HL−1000な
どがある。
Here, various ester compounds are commercially available. For example, Edenoa NPG05, PDO, PTO, PEC4, PEC of Henkel Hakusui Co., Ltd.
S, PGDO, PMO, PPE, TMNC, TMP05, TMPC, TMTC, TDO, T
TO, Katsuta Kako Co., Ltd. W-212J, VS-22, A
There are PLO-200, PU-300PL, HL-1000 and the like.

【0010】このようなエステル化合物を使用する以外
は、前述したような従来公知の方法をそのまま使用でき
る。尚、エステル化合物の使用量は結合材の種類などに
応じて適宜であるが、固形分(溶剤などの蒸発成分を除
く分)に対する割合で0.5〜5重量%程度としておく
と概ね良好である。
Except for using such an ester compound, a conventionally known method as described above can be used as it is. The amount of the ester compound to be used is appropriately determined according to the type of the binder and the like. However, it is generally preferable to set the amount to about 0.5 to 5% by weight based on the solid content (excluding the evaporation components such as solvents). is there.

【0011】[0011]

【作用】定かではないが、エステル化合物は混練時の材
料の均一分散性を向上すると思われる。材料の均一分散
性は、焼成処理後の芯の濃度−強度の逆相関関係と密接
な関係にあるからである。これは、混練を過度に長時間
あるいは激しくなすこととは異なる。過度の混練は、材
料の劣化などを招き、真の意味での材料の均一分散性の
向上とはならないからである。
[Effect] Although it is not clear, the ester compound seems to improve the uniform dispersibility of the material during kneading. This is because the uniform dispersibility of the material is closely related to the inverse correlation between the concentration and the strength of the core after the firing treatment. This is different from making the kneading too long or too vigorous. This is because excessive kneading causes deterioration of the material, and does not improve the uniform dispersibility of the material in the true sense.

【0012】[0012]

【実施例】<実施例1> ポリ塩化ビニル 50重量部 黒鉛 60重量部 ジオクチルフタレ−ト 20重量部 ジオレイン酸ネオペンチルグリコ−ル 2重量部 ステアリン酸塩 1重量部 安定剤 2重量部 メチルエチルケトン 100重量部 上記配合物を3本ロ−ルで混練し、細線状に押出成形
後、空気中で300℃まで約8時間かけて徐々に加熱
し、更に、不活性雰囲気中で1000℃まで加熱する熱
処理を施して直径約0.5mmの焼成芯体を得、これに
スピンドル油を含浸した。
<Example 1> Polyvinyl chloride 50 parts by weight Graphite 60 parts by weight Dioctyl phthalate 20 parts by weight Neopentyl glycol dioleate 2 parts by weight Stearate 1 part by weight Stabilizer 2 parts by weight Methyl ethyl ketone 100 Parts by weight The above composition was kneaded with three rolls, extruded into a fine wire, and gradually heated to 300 ° C. in air over about 8 hours, and further heated to 1000 ° C. in an inert atmosphere. Heat treatment was performed to obtain a fired core having a diameter of about 0.5 mm, which was impregnated with spindle oil.

【0013】<実施例2〜5> 実施例1において、ジオレイン酸ネオペンチルグリコ−
ルの使用量を2重量部から、0.5重量部(実施例
2)、1重量部(実施例3)、4重量部(実施例4)、
8重量部(実施例5)に変えた以外、すべて実施例1と
同様にした。
<Examples 2 to 5> In Example 1, neopentyl glycodiol dioleate was used.
From 2 parts by weight to 0.5 parts by weight (Example 2), 1 part by weight (Example 3), 4 parts by weight (Example 4),
All operations were the same as in Example 1 except that the weight was changed to 8 parts by weight (Example 5).

【0014】<実施例6〜8> 実施例1において、ジオレイン酸ネオペンチルグリコ−
ルに代えてテトラオレイン酸ペンタエリスリト−ル(実
施例6)、トリオレイン酸トリメチロ−ルプロパン(実
施例7)、ジオレイン酸プロピレングリコ−ル(実施例
8)を使用した以外、すべて実施例1と同様にした。
<Examples 6 to 8> In Example 1, neopentyl glycol dioleate was used.
Example 1 except that pentaerythritol tetraoleate (Example 6), trimethylolpropane trioleate (Example 7), and propylene glycol dioleate (Example 8) were used in place of toluene. Same as.

【0015】<比較例1> 実施例1において、ジオレイン酸ネオペンチルグリコ−
ルを使用しなかった以外、すべて実施例1と同様にし
た。
<Comparative Example 1> In Example 1, neopentyl glycodiol dioleate was used.
The procedure was the same as in Example 1 except that no metal was used.

【0016】<比較例2> 実施例1において、ジオレイン酸ネオペンチルグリコ−
ルに代えてポリメタクリル酸メチルを使用した以外、す
べて実施例1と同様にした。
<Comparative Example 2> In Example 1, neopentylglycoleate dioleate was used.
All the procedures were the same as in Example 1, except that polymethyl methacrylate was used in place of toluene.

【0017】上記各例のものについて、曲げ強さと濃度
をJIS S 6005に準じて測定した結果を表1に示
す。
Table 1 shows the results of measuring the flexural strength and the concentration of each of the above examples according to JIS S6005.

【0018】[0018]

【表1】 [Table 1]

【0019】[0019]

【発明の効果】表1において、実施例2と比較例1の値
を比較すると、曲げ強さについては実施例2の方が僅か
に小さいが、濃度については、比較例の方が大幅に小さ
い。また、実施例3や実施例7と比較例2の値を比較す
ると、実施例3や実施例7のものの曲げ強さが優れたも
のとなっている。このような一例から分かるように、本
発明によれば、濃度−強度の逆相関関係を改善した鉛筆
芯を製造することができる。
In Table 1, when the values of Example 2 and Comparative Example 1 are compared, the flexural strength of Example 2 is slightly smaller, but the concentration is much smaller in Comparative Example. . When the values of Examples 3 and 7 are compared with those of Comparative Example 2, the flexural strengths of Examples 3 and 7 are excellent. As can be seen from such an example, according to the present invention, it is possible to manufacture a pencil lead with improved density-intensity inverse correlation.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 有機結合材と体質材とを少なくとも主材
とする材料を、混練、成形後、焼成処理を施してなる鉛
筆芯の製造方法において、前記材料の一つとして、直鎖
脂肪酸と多価アルコ−ルとのエステル化合物を使用する
ことを特徴とする鉛筆芯の製造方法。
1. A method for producing a pencil lead, comprising kneading, molding and baking a material containing at least an organic binder and a building material as main components. A method for producing a pencil lead, comprising using an ester compound with a polyhydric alcohol.
JP4725991A 1991-01-28 1991-01-28 Manufacturing method of pencil lead Expired - Lifetime JP2900622B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4725991A JP2900622B2 (en) 1991-01-28 1991-01-28 Manufacturing method of pencil lead

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4725991A JP2900622B2 (en) 1991-01-28 1991-01-28 Manufacturing method of pencil lead

Publications (2)

Publication Number Publication Date
JPH04252281A JPH04252281A (en) 1992-09-08
JP2900622B2 true JP2900622B2 (en) 1999-06-02

Family

ID=12770290

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4725991A Expired - Lifetime JP2900622B2 (en) 1991-01-28 1991-01-28 Manufacturing method of pencil lead

Country Status (1)

Country Link
JP (1) JP2900622B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7217378B2 (en) 2003-09-10 2007-05-15 Council Of Scientific & Industrial Research Simple and efficient process for the preparation of pencil lead from spent pot-liners
WO2022080188A1 (en) * 2020-10-14 2022-04-21 三菱鉛筆株式会社 Pencil lead

Also Published As

Publication number Publication date
JPH04252281A (en) 1992-09-08

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