JPH02173169A - Lead of pencil - Google Patents

Lead of pencil

Info

Publication number
JPH02173169A
JPH02173169A JP33539588A JP33539588A JPH02173169A JP H02173169 A JPH02173169 A JP H02173169A JP 33539588 A JP33539588 A JP 33539588A JP 33539588 A JP33539588 A JP 33539588A JP H02173169 A JPH02173169 A JP H02173169A
Authority
JP
Japan
Prior art keywords
ester
phthalic acid
lead
phthalate
pencil
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
Application number
JP33539588A
Other languages
Japanese (ja)
Inventor
Hiroaki Okabayashi
宏明 岡林
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 JP33539588A priority Critical patent/JPH02173169A/en
Publication of JPH02173169A publication Critical patent/JPH02173169A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To obtain a lead of pencil simultaneously satisfying improvement in concentration and grab, comprising a calcined core material and a specific oily substance impregnated into pores of the calcined core material. CONSTITUTION:In lead of pencil comprising a calcined core material and an oily substance impregnated into pores of the calcined core material, a phthalic ester (e.g. phthalic acid dibenzyl ester, phthalic acid dihexadecyl ester, phthalic acid dicyclohexyl ester or phthalic acid diphenyl ester) solid at normal temperature is used at least part of the oily substance.

Description

【発明の詳細な説明】 (産業上の利用分野) 焼成芯体とこの焼成芯体の気孔中に含浸された油状物と
よりなる鉛筆芯に関する。即ち。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention relates to a pencil lead comprising a fired core and an oil impregnated into the pores of the fired core. That is.

所謂、焼成タイプの鉛筆芯に関する。This relates to a so-called baked type pencil lead.

(従来の技術) 焼成タイプの鉛筆芯は、粘土、各種合成樹脂などを結合
材として使用し、黒鉛、タルクなどの体質材や必要に応
じて使用される着色材、気孔形成材、可塑剤、溶剤など
とともに加圧ニーダ−、ヘンシェルミキサー、3本ロー
ルなどで均一分散させた後、高温熱処理して得られる多
孔質の焼成芯体に種々物質を種々目的で含浸して製造さ
れている。
(Conventional technology) Baked type pencil leads use clay, various synthetic resins, etc. as binding materials, as well as extenders such as graphite and talc, colorants, pore-forming agents, plasticizers, etc., as necessary. It is manufactured by impregnating a porous fired core with various substances for various purposes, which is obtained by uniformly dispersing it together with a solvent using a pressure kneader, Henschel mixer, three rolls, etc., and then subjecting it to high-temperature heat treatment.

ここにおける含浸物の代表的なものが油状物であり、一
般に、濃度向上に役立つ。また。
A typical impregnating material here is an oily substance, which is generally useful for increasing concentration. Also.

筆記面との定着性、即ち、筆跡の汚れ難さを向上する上
でも役立つ。ちなみに、油状物の一例としては、スピン
ドル油、シリコーン油、流動パラフィン、マイクロクリ
スタリンワックス、モンタンワックス、ボヘミアワック
ス、パラフィンワックス、カルナバワックス、綿臘、蜜
臘などを挙げられる。融点、沸点など様々であり、常温
で液体状のものもあれば固体状のものもある。
It is also useful in improving the adhesion to the writing surface, that is, the resistance to staining of handwriting. Incidentally, examples of oily substances include spindle oil, silicone oil, liquid paraffin, microcrystalline wax, montan wax, bohemia wax, paraffin wax, carnauba wax, cotton wax, and beeswax. They have various melting points, boiling points, etc., and some are liquid at room temperature while others are solid.

(発明が解決しようとする課題) 油状物のもたらす濃度向上と定着性向上とは常に両立す
るものではない。即ち、濃度向上度の高い油上物は定着
性向上皮が低いという一般的傾向にある。具体的には、
融点の低いものは濃度向上度が高い反面、定着性向上皮
が低く、融点の高いものは定着性向上皮が高い反面、濃
度向上度が低いという傾向にある。
(Problems to be Solved by the Invention) Improving the density brought about by oily substances and improving fixing properties are not always compatible. That is, there is a general tendency that oily substances with a high degree of improvement in concentration have a low degree of improvement in fixability. in particular,
Those with a low melting point tend to have a high degree of improvement in density, but have a low degree of improvement in fixability, and those with a high melting point have a high degree of improvement in fixability, but have a low degree of improvement in density.

この逆相関関係を破り、定着性向上の点で同等ならば濃
度が一層向上し、濃度向上の点で同等ならば定着性が一
層向上した鉛筆芯を提供することが本発明の目的である
It is an object of the present invention to break this inverse relationship and provide a pencil lead that has an even higher density if the improvement in fixing performance is the same, and a pencil lead that has an even better fixability if the improvement in the density is the same.

(課題を解決するための手段) 油状物として常温で固体状のフタル酸エステルを使用す
る。このフタル酸エステルは他の油状物と併用できる。
(Means for solving the problem) A phthalate ester that is solid at room temperature is used as the oil. This phthalate ester can be used in combination with other oils.

即ち、本発明は、焼成芯体とこの焼成芯体の気孔中に含
浸された油状物とよりなる鉛筆芯において、前記油状物
の少なくとも一部として、常温で固体状のフタル酸エス
テルを有してなる鉛筆芯を要旨とする。
That is, the present invention provides a pencil lead comprising a fired core and an oily substance impregnated into the pores of the fired lead, which contains a phthalate ester that is solid at room temperature as at least a part of the oily substance. The main point is the pencil lead.

以下、詳述する。The details will be explained below.

常温で固体状のフタル酸エステルの一例としては、フタ
ル酸ジベンジルエステル、フタル酸ジヘキサデシルエス
テル、フタル酸ジシクロヘキシルエステル、フタル酸ジ
フェニルエステル、フタル酸モノメチルエステル、フタ
ル酸モノフェニルエステル、フタル酸モノシクロヘキシ
ルエステルなど挙げられる。このような常温で固体状の
フタル酸エステルは、分子配列が規則的となるよう固化
し、また、加圧されると容易に眉間剥離を生じるという
性質を有する。
Examples of phthalate esters that are solid at room temperature include dibenzyl phthalate, dihexadecyl phthalate, dicyclohexyl phthalate, diphenyl phthalate, monomethyl phthalate, monophthalate monophthalate, and monophthalate. Examples include cyclohexyl ester. Such phthalate esters, which are solid at room temperature, solidify so that the molecular arrangement becomes regular, and also have the property of easily causing peeling between the eyebrows when pressurized.

このフタル酸エステルを適宜気孔率の焼成芯体に含浸す
る。含浸するにあたっては適宜加熱それに必要ならば加
圧などをなせばよい。
This phthalate ester is impregnated into a fired core having an appropriate porosity. For impregnation, heat may be applied as appropriate and pressure may be applied if necessary.

尚、併用できる他の油状物は前述したものなど適宜であ
るが、相溶性のあるものはそれだけ含浸も容易になる。
Note that other oily substances that can be used in combination are suitable, such as those mentioned above, and the more compatible they are, the easier the impregnation will be.

また、含浸物としては油状物以外のものもあり、それぞ
れの使用目的に応じて併用すればよい。
In addition, there are impregnating substances other than oily substances, and they may be used in combination depending on the purpose of use.

(実施例) 以下、単に、「部」とあるのは「重量部」を示す。(Example) Hereinafter, "parts" simply indicate "parts by weight."

〈実施例1〉 塩化ビニル酢酸ビニル共重合物  30部黒鉛    
          50部カーボンブラック    
     5部ステアリン酸塩          1
部フタル酸ジオクチル       10部上記材料を
3本ロールで十分に混練後、細線状に押出成形し、空気
中で300℃まで熱処理後、不活性雰囲気中で950℃
まで熱処理して呼び径0.5++aのシャープペンシル
用の焼成芯体を得た。これを100℃に加熱したフタル
酸ジベンジルエステル中に2時間浸漬し、余剰分を除去
して鉛筆芯とした。
<Example 1> Vinyl chloride vinyl acetate copolymer 30 parts graphite
50 parts carbon black
5 parts stearate 1
Dioctyl phthalate 10 parts The above materials were thoroughly kneaded with three rolls, extruded into a thin wire, heat-treated in air to 300°C, and then heated to 950°C in an inert atmosphere.
A fired core for a mechanical pencil with a nominal diameter of 0.5++a was obtained. This was immersed in phthalic acid dibenzyl ester heated to 100° C. for 2 hours, and the excess was removed to obtain a pencil lead.

〈実施例2〜4〉 実施例1において、焼成芯体をフタル酸ジベンジルエス
テルに浸漬する代りに、フタル酸ジヘキサデシルエステ
ル、フタル酸ジシクロヘキシルエステル、フタル酸ジフ
ェニルエステルにそれぞれ浸漬した以外、す入で実施例
1と同様にした。
<Examples 2 to 4> In Example 1, the fired core was immersed in dihexadecyl phthalate, dicyclohexyl phthalate, and diphenyl phthalate instead of immersing the fired core in dibenzyl phthalate. The procedure was the same as in Example 1.

〈実施例5〉 実施例1において、焼成芯体を100℃のフタル酸ジベ
ンジルエステルに浸漬する代りに、130℃のフタル酸
モノフェニルエステルに浸漬した以外、すべて実施例1
と同様にした。
<Example 5> In Example 1, the fired core was immersed in phthalic acid monophenyl ester at 130°C instead of immersing it in phthalic acid monophenyl ester at 100°C.
I did the same thing.

〈実施例6〉 実施例1において、焼成芯体をフタル酸ジベンジルエス
テルに浸漬する代りに、フタル酸ジフェニルエステルと
スピンドル油との等重量混合物に浸漬した以外、すべて
実施例1と同様にした。
<Example 6> Everything was the same as in Example 1, except that instead of immersing the fired core in phthalic acid dibenzyl ester, it was immersed in an equal weight mixture of phthalic acid diphenyl ester and spindle oil. .

〈実施例7〉 実施例1において、焼成芯体をフタル酸ジベンジルエス
テルに浸漬する代りに、フタル酸ジヘキサデシルエステ
ルとマイクロクリスタリンワックスとの4:1(重量)
混合物に浸漬した以外、す八で実施例1と同様にした。
<Example 7> In Example 1, instead of immersing the fired core in dibenzyl phthalate, dihexadecyl phthalate and microcrystalline wax were mixed in a ratio of 4:1 (by weight).
The same procedure as in Example 1 was carried out with Suhachi, except that it was immersed in the mixture.

〈実施例8〜10) シャープペンシル用として市販されている炭素骨格を有
する製品2種とレッドホルダー用として市販されている
粘土骨格を有する製品1種の計3種について、メチルエ
チルケ1−ンとアセ1〜ンとによって十分に脱油後、こ
れを実施例3における焼成芯体に代えて使用した以外、
すべて実施例3と同様にした。
(Examples 8 to 10) For a total of three products, two products with a carbon skeleton commercially available for mechanical pencils and one product with a clay skeleton commercially available for red holders, methyl ethylkene and acetic acid were used. After sufficient deoiling by steps 1 to 1, this was used in place of the fired core in Example 3.
Everything was the same as in Example 3.

く比較例1〜4〉 実施例1,8〜10において、焼成芯体をフタル酸ジベ
ンジルエステルに浸漬する代りに、スピンドル油に浸漬
した以外、すべてそれぞれの実施例と同様にした。
Comparative Examples 1 to 4 In Examples 1 and 8 to 10, all the procedures were the same as in Examples 1 and 8 to 10, except that the fired core was immersed in spindle oil instead of immersed in phthalic acid dibenzyl ester.

く比較例5〜8〉 実施例1.8〜10において、焼成芯体を100℃のフ
タル酸ジベンジルエステルに浸漬する代りに、120℃
のモンタンワックスに浸漬した以外、すべてそれぞれの
実施例と同様にした。
Comparative Examples 5 to 8> In Examples 1.8 to 10, instead of immersing the fired core in phthalic acid dibenzyl ester at 100 °C,
Everything was the same as in each example except that it was dipped in montan wax.

(発明の効果) 各側で得たものについて、濃度と定着性を調べた結果を
表−1に示す。
(Effects of the Invention) Table 1 shows the results of examining the density and fixing properties of the samples obtained on each side.

(以下、余白) 表−1 (注)濃度は、LIS S 6005に準じて測定し、
また、定着性はバライタ紙に荷重400gで画線した筆
記部の反射率をα、筆記部を一定条件でこすり、筆記部
外の汚れたところの反射率をβとしたとき、 (100−β)÷(100−α)X100として求めた
。ここで、値が小さいほど定着性がよい。
(Hereafter, blank space) Table 1 (Note) Concentration is measured according to LIS S 6005,
In addition, the fixability is determined by the following formula: (100-β) where α is the reflectance of the writing area drawn on baryta paper with a load of 400 g, and β is the reflectance of the dirty area outside the writing area when the writing area is rubbed under certain conditions. )÷(100-α)X100. Here, the smaller the value, the better the fixing performance.

表−1より判るように、本発明によると。As can be seen from Table 1, according to the present invention.

濃度と定着性の逆相関関係を改善された鉛筆芯たり得る
A pencil lead with an improved inverse relationship between density and fixability can be obtained.

Claims (1)

【特許請求の範囲】 焼成芯体とこの焼成芯体の気孔中に含浸さ れた油状物とよりなる鉛筆芯において、前記油状物の少
なくとも一部として、常温で固体状のフタル酸エステル
を有してなる鉛筆芯。
[Scope of Claims] A pencil lead consisting of a fired core and an oily substance impregnated into the pores of the fired lead, which contains a phthalate ester that is solid at room temperature as at least a part of the oily substance. Pencil lead.
JP33539588A 1988-12-27 1988-12-27 Lead of pencil Pending JPH02173169A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP33539588A JPH02173169A (en) 1988-12-27 1988-12-27 Lead of pencil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP33539588A JPH02173169A (en) 1988-12-27 1988-12-27 Lead of pencil

Publications (1)

Publication Number Publication Date
JPH02173169A true JPH02173169A (en) 1990-07-04

Family

ID=18288063

Family Applications (1)

Application Number Title Priority Date Filing Date
JP33539588A Pending JPH02173169A (en) 1988-12-27 1988-12-27 Lead of pencil

Country Status (1)

Country Link
JP (1) JPH02173169A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017115088A (en) * 2015-12-25 2017-06-29 株式会社トンボ鉛筆 Pencil lead

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2017115088A (en) * 2015-12-25 2017-06-29 株式会社トンボ鉛筆 Pencil lead

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