JP3035157B2 - Manufacturing method of non-fired pencil lead - Google Patents
Manufacturing method of non-fired pencil leadInfo
- Publication number
- JP3035157B2 JP3035157B2 JP6140490A JP14049094A JP3035157B2 JP 3035157 B2 JP3035157 B2 JP 3035157B2 JP 6140490 A JP6140490 A JP 6140490A JP 14049094 A JP14049094 A JP 14049094A JP 3035157 B2 JP3035157 B2 JP 3035157B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- lubricant
- softening point
- pencil lead
- 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
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- Inks, Pencil-Leads, Or Crayons (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は鉛筆、シャープペンシル
用の非焼成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 producing a non-fired pencil lead for pencils and mechanical pencils.
【0002】[0002]
【従来の技術】従来の非焼成鉛筆芯は、結合剤である有
機高分子物質を必要に応じて溶剤及び/又は可塑剤類で
溶解又は膨潤させて着色剤、体質剤、潤滑剤等と共に混
練、成形し、必要に応じて加えられた溶剤及び/又は可
塑剤類を乾燥除去して製造されている。2. Description of the Related Art A conventional non-fired pencil lead is prepared by dissolving or swelling an organic polymer substance as a binder with a solvent and / or a plasticizer, if necessary, and kneading it together with a coloring agent, a filler, a lubricant and the like. It is manufactured by drying and removing the solvent and / or plasticizer added as necessary.
【0003】ここで結合剤としては、ポリビニルアルコ
ール、カルボキシメチルセルロース、ポリ塩化ビニル、
塩化ビニル共重合体、繊維素系樹脂、ポリスチレン、ス
チレン共重合体、エポキシ樹脂等の有機高分子物質の一
種又は二種以上が選択して用いられている。[0003] As the binder, polyvinyl alcohol, carboxymethyl cellulose, polyvinyl chloride,
One or more organic polymer substances such as a vinyl chloride copolymer, a cellulose resin, a polystyrene, a styrene copolymer, and an epoxy resin are selectively used.
【0004】また、潤滑剤としては、一般に木ろう、カ
ルナバワックス等の天然ワックス、モンタンワックス、
ポリエチレンワックス等の合成ワックス、ステアリン
酸、ラウリン酸等の高級脂肪酸、ステアリン酸亜鉛、ス
テアリン酸カルシウム、ミリスチン酸リチウム等の金属
石鹸等が使用されている。潤滑剤として金属石鹸を用い
たものとして、特公昭47−48564号公報があり、
更に潤滑剤としてミリスチン酸リチウムを使用したもの
として、特公平6−6690号公報が知られている。[0004] Examples of the lubricant include natural waxes such as wood wax and carnauba wax, montan wax, and the like.
Synthetic waxes such as polyethylene wax, higher fatty acids such as stearic acid and lauric acid, metal soaps such as zinc stearate, calcium stearate and lithium myristate are used. Japanese Patent Publication No. 47-48564 discloses a method using metal soap as a lubricant.
Further, Japanese Patent Publication No. 6-6690 discloses a method using lithium myristate as a lubricant.
【0005】非焼成鉛筆芯において、結合剤は構造強度
を発現させるには不可欠の材料であり、他の配合組成物
との混練性や強度発現のために化学的な親和性を考慮し
て選択される必要がある。[0005] In a non-fired pencil lead, a binder is an indispensable material for developing structural strength, and is selected in consideration of chemical affinity for kneading with other compounding compositions and developing strength. Need to be done.
【0006】一方、潤滑剤は筆記時の書味を滑らかに
し、描線濃度の向上を図るためには必要不可欠な材料で
あるが、曲げ強度を著しく低下させてしまうことが起こ
り易く、結合剤との相互作用を検討する必要がある。一
般に、結合剤としては、その強靭性と易加工性を利用し
てニトロセルロースが用いられている。また潤滑剤とし
てはリチウム石鹸に代表される210℃以上の高軟化点
を有するものを用いると、曲げ強度の低下をある程度押
さえることが可能であることが知られている。[0006] On the other hand, a lubricant is an indispensable material for smoothing the writing quality at the time of writing and for improving the drawing line density. However, the bending strength is liable to be remarkably reduced. It is necessary to consider the interaction. Generally, nitrocellulose is used as a binder, taking advantage of its toughness and easy processability. It is known that the use of a lubricant having a high softening point of 210 ° C. or higher typified by lithium soap can suppress a decrease in bending strength to some extent.
【0007】しかし、ニトロセルロースは火薬類に分類
される物質であるため消防法上、取扱いに厳密な注意を
払わなければならない。又リチウム石鹸単独の潤滑剤で
は、着色性が劣化し、十分な描線濃度を発現させること
ができない等の欠点がある。However, since nitrocellulose is a substance classified as explosives, strict attention must be paid to its handling under the Fire Service Law. Further, the use of a lubricant containing lithium soap alone has disadvantages such as deterioration of coloring properties and the inability to develop a sufficient drawing line density.
【0008】[0008]
【発明が解決しようとする課題】本発明の目的は、従来
の方法では得られなかった、十分な曲げ強度と優れた着
色性を併せ持つ非焼成鉛筆芯の製造方法を提供すること
である。SUMMARY OF THE INVENTION An object of the present invention is to provide a method for producing a non-fired pencil lead having sufficient bending strength and excellent coloring properties, which cannot be obtained by the conventional methods.
【0009】[0009]
【課題を解決するための手段】本発明者は、前記の課題
を解決するために鋭意研究を行った結果、結合剤と、着
色剤と、体質剤と、潤滑剤とを主剤とする配合組成物を
混練、成形して成る非焼成鉛筆芯の製造方法において、
結合剤の少なくとも一部としてセルロイドを用いると共
に、潤滑剤の少なくとも一部として、リチウム石鹸及び
脂肪酸アミドを併用すること、好ましくは脂肪酸アミド
は軟化点が110℃以下のものを特定して用いることに
よって、十分な曲げ強度と優れた着色性を併せ持つ非焼
成鉛筆芯を製造することができることを知見し、本発明
を完成した。Means for Solving the Problems The present inventor has conducted intensive studies to solve the above-mentioned problems, and as a result, has found that a compounding composition comprising a binder, a coloring agent, a constitutional agent, and a lubricant as main components. In a method for producing a non-fired pencil lead formed by kneading and molding a product,
Celluloid is used as at least a part of the binder, and lithium soap and a fatty acid amide are used in combination as at least a part of the lubricant. Preferably, the fatty acid amide has a softening point of 110 ° C. or less. The present inventors have found that a non-fired pencil lead having both sufficient bending strength and excellent coloring properties can be manufactured, and the present invention has been completed.
【0010】次に本発明の配合組成物について、詳細に
説明する。結合剤としては、少なくとも一部としてセル
ロイドを用いる。一般に、セルロイドは硝化度11%前
後、重合度200〜600程度のニトロセルロースに2
0〜35%の樟脳を混和したもので、ニトロセルロース
と比べて格段に火薬特性が少ないが、結合剤として必要
な強靭性を有する。本発明ではセルロイドの種類につい
ては格別には限定しない。また、本発明では結合剤とし
て、必要に応じてセルロイド以外の有機高分子物質を併
用しても良い。例えば、酢酸ビニル共重合体。繊維素系
樹脂、ポリスチレン、スチレン共重合体、エポキシ樹脂
等の有機高分子物質の一種又は二種以上を選択すること
が可能であるが、他の配合組成物との混練性を考慮する
と、セルロイドの良溶媒であるアルコール類、エステル
類、ケトン類等に可溶である種類が好ましい。併用樹脂
の配合割合はセルロイドの優れた性質を消失させない目
的から、結合剤全量に対して30重量%以下に押さえる
ことが好ましい。Next, the compounding composition of the present invention will be described in detail. Celluloid is used as at least a part of the binder. In general, celluloid is added to nitrocellulose having a nitrification degree of about 11% and a polymerization degree of about 200 to 600.
It is a mixture of 0-35% camphor and has much less explosive properties than nitrocellulose, but has the toughness required as a binder. In the present invention, the type of celluloid is not particularly limited. In the present invention, an organic polymer substance other than celluloid may be used in combination as a binder, if necessary. For example, vinyl acetate copolymer. It is possible to select one or more of organic polymer substances such as cellulose resin, polystyrene, styrene copolymer, epoxy resin, etc. Preferred are those soluble in alcohols, esters, ketones and the like, which are good solvents. The mixing ratio of the combined resin is preferably kept at 30% by weight or less based on the total amount of the binder for the purpose of not losing the excellent properties of celluloid.
【0011】着色剤としては無機顔料、有機顔料のいず
れをも使用することができる。体質剤としては、タル
ク、セリサイト、カオリナイト、ベントナイト、ウォラ
ストナイト、炭酸カルシウム、窒化硼素、炭酸カリウム
等の鉛筆芯に通常使用されるものを一種又は二種以上選
択する。As the colorant, either an inorganic pigment or an organic pigment can be used. As the extender, one or more of talc, sericite, kaolinite, bentonite, wollastonite, calcium carbonate, boron nitride, potassium carbonate, etc., which are commonly used in pencil cores, are selected.
【0012】本発明では潤滑剤の少なくとも一部とし
て、リチウム石鹸及び脂肪酸アミドを用いる。脂肪酸ア
ミドは軟化点が110℃以下であるものを特定して用い
ることが好ましい。リチウム石鹸はステアリン酸リチウ
ム、ヒドロキシステアリン酸リチウム、ミリスチン酸リ
チウム等に代表される軟化点が210℃を超える金属石
鹸であり、本発明ではその一種又は二種以上を選択して
用いる。In the present invention, lithium soap and fatty acid amide are used as at least a part of the lubricant. It is preferable that a fatty acid amide having a softening point of 110 ° C. or lower be specified and used. Lithium soap is a metal soap having a softening point of more than 210 ° C. represented by lithium stearate, lithium hydroxystearate, lithium myristate and the like. In the present invention, one or two or more thereof are selected and used.
【0013】脂肪酸アミドとしは第1アミド、第2アミ
ドのいずれも使用可能であり、その一種又は二種以上を
用いるが、着色性を向上し、描線濃度を増すために好ま
しくは軟化点が110℃以下、より好ましくは、曲げ強
度と着色力のバランスをとる上で軟化点が70〜100
℃の脂肪酸アミドを選定すると良い。軟化点70℃以下
の脂肪酸アミドでは曲げ強度の低下が生じやすく、軟化
点100℃を超える脂肪酸アミドでは着色力に劣る傾向
がある。軟化点が70〜100℃の脂肪酸アミドの例と
しては、ラウリン酸アミド(80℃)、ステアリン酸ア
ミド(100℃)、エルカ酸アミド(82℃)、N‐オ
レイルステアリン酸アミド(74℃)、N‐ステアリル
ステアリン酸アミド(95℃)等をあげることができ
る。As the fatty acid amide, either a primary amide or a secondary amide can be used, and one or two or more of them can be used. In order to improve the coloring property and increase the drawing density, the softening point is preferably 110 or more. ° C. or lower, more preferably, a softening point of 70 to 100 for balancing bending strength and coloring power.
It is good to select fatty acid amide of ° C. A fatty acid amide having a softening point of 70 ° C. or lower tends to cause a decrease in bending strength, and a fatty acid amide having a softening point of more than 100 ° C. tends to have poor coloring power. Examples of the fatty acid amide having a softening point of 70 to 100 ° C. include lauric amide (80 ° C.), stearic amide (100 ° C.), erucamide (82 ° C.), N-oleyl stearamide (74 ° C.), N-stearyl stearamide (95 ° C.) and the like.
【0014】また、本発明においては必要に応じて一般
の天然ワックス、合成ワックス、高級脂肪酸、金属石鹸
等の潤滑剤を併用しても良い。配合組成物に占める潤滑
剤の総量を100重量部とした場合、リチウム石鹸:2
0〜90重量部、好ましくは35〜85重量部、脂肪酸
アミド:10〜80重量部、好ましくは25〜75重量
部、併用する潤滑剤:0〜40重量部、好ましくは0〜
25重量部という配合比率とすることが好適である。In the present invention, if necessary, general lubricants such as natural waxes, synthetic waxes, higher fatty acids and metal soaps may be used in combination. When the total amount of the lubricant in the composition is 100 parts by weight, lithium soap: 2
0-90 parts by weight, preferably 35-85 parts by weight, fatty acid amide: 10-80 parts by weight, preferably 25-75 parts by weight, lubricant used together: 0-40 parts by weight, preferably 0-0 parts by weight
It is preferable that the mixing ratio is 25 parts by weight.
【0015】上記配合組成物から非焼成鉛筆芯を得るに
は、先ず、所定量を計量して分散、混練する。分散方法
としては、セルロイドを溶剤に溶解した後に他の配合材
料を加えた方が、その後の混練工程を容易にする。次
に、混練物を成形機を用いて所定の形状に成形し、溶剤
を乾燥して、製品を得る。In order to obtain a non-fired pencil lead from the above composition, first, a predetermined amount is measured, dispersed and kneaded. As a dispersing method, it is easier to dissolve the celluloid in a solvent and then add another compounding material to facilitate the subsequent kneading step. Next, the kneaded material is formed into a predetermined shape using a forming machine, and the solvent is dried to obtain a product.
【0016】[0016]
【作用】本発明の製造方法によって得られる非焼成鉛筆
芯は、結合剤としては、必要な強靭性を有し、且つ取り
扱いも安全性の高いセルロイドを選択し、潤滑剤として
は、曲げ強度低下を抑制する性質を有する高軟化点潤滑
剤であるリチウム石鹸と、着色力を向上させるために、
セルロイド中のニトロセルロースのニトロ基と親和性の
大きい極性基を有する脂肪酸アミドを選択することで、
著しい曲げ強度低下を誘引せずに描線濃度が向上する。The non-fired pencil lead obtained by the production method of the present invention has a required toughness as a binder, and a celluloid which is highly safe to handle is selected. Lithium soap is a high softening point lubricant having the property of suppressing, in order to improve the coloring power,
By selecting a fatty acid amide having a polar group with high affinity with the nitro group of nitrocellulose in celluloid,
The drawing line density is improved without inducing a significant decrease in bending strength.
【0017】[0017]
【実施例】以下に実施例によって、本発明を更に具体的
に説明するが本発明はこの実施例によって何等限定され
るものではない。EXAMPLES The present invention will be described more specifically with reference to the following examples, but the present invention is not limited to these examples.
【0018】(実施例1)硝化度11%、落球法による
粘度が120秒のニトロセルロース75重量%と樟脳2
5重量%とで混和、製造したセルロイド30重量部を酢
酸エチル100重量部に溶解した後に、フタロシアニン
ブルー15重量部、チタン酸カリウム繊維35重量部、
潤滑剤としてステアリン酸リチウム13重量部、及び軟
化点82℃のエルカ酸アミド7重量部を計量してワーナ
ーミキサーに投入、分散後、3本ロールにて混練と同時
に酢酸エチル分を調整し、押出成形機を用いて成形後、
酢酸エチルを乾燥させて直径0.5mmの青色芯を得た。EXAMPLE 1 75% by weight of nitrocellulose having a nitrification degree of 11% and a viscosity of 120 seconds by a falling ball method and camphor 2
After dissolving 30 parts by weight of the celluloid prepared and mixed with 5% by weight in 100 parts by weight of ethyl acetate, 15 parts by weight of phthalocyanine blue, 35 parts by weight of potassium titanate fiber,
13 parts by weight of lithium stearate as a lubricant and 7 parts by weight of erucamide having a softening point of 82 ° C. were put into a Warner mixer, dispersed, kneaded with a three-roll mill and simultaneously adjusted with ethyl acetate, and extruded. After molding using a molding machine,
The ethyl acetate was dried to obtain a blue core having a diameter of 0.5 mm.
【0019】(比較例1)実施例1の配合組成物のう
ち、脂肪酸アミドを軟化点123℃のキシリレンビスス
テアリン酸アミドに置き換えた他は同一の配合組成とし
て、直径0.5mmの青色芯を得た。Comparative Example 1 A blue core having a diameter of 0.5 mm was the same as the composition of Example 1, except that the fatty acid amide was replaced by xylylene bisstearic acid amide having a softening point of 123 ° C. I got
【0020】(比較例2)実施例1の配合組成物のう
ち、潤滑剤をステアリン酸リチウム1種類、20重量部
とした他は同一の配合組成として、直径0.5mmの青色
芯を得た。Comparative Example 2 A blue core having a diameter of 0.5 mm was obtained in the same composition as in Example 1, except that the lubricant was lithium lithium stearate of one kind and 20 parts by weight. .
【0021】(比較例3)実施例1の配合組成物のう
ち、潤滑剤を軟化点120℃のステアリン酸亜鉛1種
類、20重量部とした他は同一の配合組成として、直径
0.5mmの青色芯を得た。COMPARATIVE EXAMPLE 3 The same composition as in Example 1 except that the lubricant was one kind of zinc stearate having a softening point of 120 ° C. and 20 parts by weight was used. A blue core was obtained.
【0022】(比較例4)実施例1の配合組成物のう
ち、潤滑剤を軟化点82℃のエルカ酸アミド1種類、2
0重量部とした他は同一の配合組成として、直径0.5
mmの青色芯を得た。(Comparative Example 4) In the composition of Example 1, one kind of erucamide having a softening point of 82 ° C was used.
0 parts by weight and the same composition except that the diameter is 0.5
mm blue core was obtained.
【0023】(実施例2)硝化度11%、落球法による
粘度が120秒のニトロセルロース75重量%と樟脳2
5重量%とで混和、製造したセルロイド20重量部を酢
酸エチル100重量部に溶解した後に、フタロシアニン
ブルー15重量部、チタン酸カリウム繊維20重量部、
タルク20重量部、潤滑剤としてヒドロキシステアリン
酸リチウム15重量部、及び軟化点74℃のN−オレイ
ルステアリン酸アミド10重量部を計量してワーナーミ
キサーに投入、分散後、3本ロールにて混練と同時に酢
酸エチル分を調整し、押出成形機を用いて成形後、酢酸
エチルを乾燥させて直径3mmの青色芯を得た。Example 2 75% by weight of nitrocellulose having a nitrification degree of 11% and a viscosity of 120 seconds by a falling ball method and camphor 2
After dissolving 20 parts by weight of the celluloid prepared and mixed with 5% by weight in 100 parts by weight of ethyl acetate, 15 parts by weight of phthalocyanine blue, 20 parts by weight of potassium titanate fiber,
20 parts by weight of talc, 15 parts by weight of lithium hydroxystearate as a lubricant, and 10 parts by weight of N-oleylstearic acid amide having a softening point of 74 ° C. were put into a Warner mixer, dispersed and kneaded with three rolls. At the same time, the content of ethyl acetate was adjusted and molded using an extruder, and then the ethyl acetate was dried to obtain a blue core having a diameter of 3 mm.
【0024】(比較例5)実施例2の配合組成物のう
ち、脂肪酸アミドを軟化点123℃のキシリレンビスス
テアリン酸アミドに置き換えた他は同一の配合組成とし
て、直径3mmの青色芯を得た。Comparative Example 5 A blue core having a diameter of 3 mm was obtained in the same composition as in Example 2, except that the fatty acid amide was replaced with xylylene bisstearic acid amide having a softening point of 123 ° C. Was.
【0025】(比較例6)実施例2の配合組成物のう
ち、潤滑剤をステアリン酸リチウム1種類、25重量部
とした他は同一の配合組成として、直径3mmの青色芯を
得た。Comparative Example 6 A blue core having a diameter of 3 mm was obtained in the same composition as in Example 2, except that the lubricant was changed to one kind of lithium stearate and 25 parts by weight.
【0026】(比較例7)実施例2の配合組成物のう
ち、潤滑剤を軟化点120℃のステアリン酸亜鉛1種
類、25重量部とした他は同一の配合組成として、直径
3mmの青色芯を得た。(Comparative Example 7) A blue core having a diameter of 3 mm was prepared in the same manner as in Example 2 except that one kind of zinc stearate having a softening point of 120 ° C. and 25 parts by weight were used as a lubricant. I got
【0027】(比較例8)実施例2の配合組成物のう
ち、潤滑剤を軟化点74℃のN−オレイルステアリン酸
アミド1種類、25重量部とした他は同一の配合組成と
して、直径3mmの青色芯を得た。Comparative Example 8 The same composition as in Example 2 except that the lubricant was one kind of N-oleylstearic amide having a softening point of 74 ° C. and 25 parts by weight was used. Blue core was obtained.
【0028】実施例1〜2、比較例1〜8で得られた非
焼成鉛筆芯の曲げ強度、及び描線濃度についての測定結
果を表1に示す。尚、曲げ強度の測定はJIS S 6
005に準じ、描線濃度は画線試験までをJIS S
6005に準じ、目視で判定した。Table 1 shows the measurement results of the bending strength and the drawing line density of the non-fired pencil leads obtained in Examples 1 and 2 and Comparative Examples 1 to 8. The bending strength was measured according to JIS S6
According to 005, JIS S
The determination was made visually according to 6005.
【0029】[0029]
【表1】 [Table 1]
【0030】[0030]
【発明の効果】本発明の方法による非焼成鉛筆芯は上記
の試験結果でも明らかなように、従来の方法では得られ
なかった、十分な曲げ強度と優れた着色性を持つ。The unfired pencil lead obtained by the method of the present invention has a sufficient bending strength and excellent coloring properties, which cannot be obtained by the conventional method, as is apparent from the above test results.
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) C09D 13/00 ──────────────────────────────────────────────────続 き Continued on front page (58) Field surveyed (Int. Cl. 7 , DB name) C09D 13/00
Claims (2)
とを主剤とする配合成分を混練、成形して成る非焼成鉛
筆芯の製造方法において、結合剤の少なくとも一部とし
てセルロイドを用いると共に、潤滑剤の少なくとも一部
としてリチウム石鹸及び脂肪酸アミドを併用することを
特徴とする非焼成鉛筆芯の製造方法。1. A method for producing a non-fired pencil lead, comprising kneading and molding a compounding component mainly comprising a binder, a colorant, a constitution agent and a lubricant, wherein at least a part of the binder is celluloid. A method for producing a non-fired pencil lead, comprising using lithium soap and a fatty acid amide as at least a part of a lubricant.
である請求項1記載の非焼成鉛筆芯の製造方法。2. The method according to claim 1, wherein the fatty acid amide has a softening point of 110 ° C. or lower.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6140490A JP3035157B2 (en) | 1994-06-22 | 1994-06-22 | Manufacturing method of non-fired pencil lead |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6140490A JP3035157B2 (en) | 1994-06-22 | 1994-06-22 | Manufacturing method of non-fired pencil lead |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH083503A JPH083503A (en) | 1996-01-09 |
JP3035157B2 true JP3035157B2 (en) | 2000-04-17 |
Family
ID=15269836
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6140490A Expired - Lifetime JP3035157B2 (en) | 1994-06-22 | 1994-06-22 | Manufacturing method of non-fired pencil lead |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3035157B2 (en) |
-
1994
- 1994-06-22 JP JP6140490A patent/JP3035157B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH083503A (en) | 1996-01-09 |
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