JP3438433B2 - eraser - Google Patents

eraser

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JP3438433B2
JP3438433B2 JP25474795A JP25474795A JP3438433B2 JP 3438433 B2 JP3438433 B2 JP 3438433B2 JP 25474795 A JP25474795 A JP 25474795A JP 25474795 A JP25474795 A JP 25474795A JP 3438433 B2 JP3438433 B2 JP 3438433B2
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eraser
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vinyl chloride
erased
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JPH0971096A (en
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安宏 高橋
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Pentel Co Ltd
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Pentel Co Ltd
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Description

【発明の詳細な説明】 【0001】 【発明の属する技術分野】本発明は、鉛筆やシャープペ
ンシル等の筆跡を消去するための消しゴムに関する物で
あり、更に詳細には少ない消去回数で消し屑が一つにま
とまる消しゴムのに関する。 【0002】 【従来の技術】従来、消しゴムは、基材樹脂として塩化
ビニル樹脂や塩化ビニルの共重合体を用いた塩化ビニル
系のもの、主に天然ゴムを用いた天然ゴム系のもの、熱
可塑性エラストマ−又は合成ゴムを用いたエラストマ−
・合成ゴム系のものが知られている。塩化ビニル樹脂を
基材樹脂とする消しゴムは、塩化ビニル樹脂と可塑剤、
必要に応じて充填剤やその他の添加剤を加えて混合した
ペースト状のプラスチゾルを加熱して塩化ビニル樹脂に
可塑剤を吸収させることによって作られる。天然ゴムを
基材樹脂とする消しゴムは、天然ゴムとサブ、充填材を
混合し加硫して作られる。熱可塑性エラストマ−又は合
成ゴムを基材樹脂とする消しゴムは、熱可塑性エラスト
マ−又は合成ゴムと充填材、必要に応じて軟化剤を混合
して未加硫のまま加熱成型して作られる。ところで、消
しゴムは紙面との擦過によって摩耗することが必要であ
る。これは、以下の理由による。鉛筆やシャープペンシ
ルの筆跡は、紙との擦過で摩耗した鉛筆やシャープペン
シルの芯の粉が紙面に付着したものである。この芯の摩
耗粉が消しゴム表面や消し屑表面に再付着することによ
り紙面から取り除かれて、筆跡が消去される。この時消
しゴムが摩耗して消し屑が発生しないと、消しゴム表面
が芯の摩耗粉で覆われて、それ以上芯の摩耗粉を付着す
ることが出来ず、それ以上筆跡を消去することが出来な
いばかりか、一旦消しゴムに付着した芯の摩耗粉が再度
紙面に付着するため紙面を汚すといったことが起こる。
このため、消しゴムは紙との擦過で摩耗して消し屑を出
すことが必要である。このような特性を得るため、例え
ば、塩化ビニル系消しゴムにおいては通常の塩化ビニル
樹脂成型品に比べ加熱温度を低くして成形する。このこ
とは特公昭32−8220号公報によって知られてい
る。即ち、特公昭32−8220号公報には塩化ビニル
樹脂に対してその重量の80〜160重量%の可塑剤を
添加し、比較的低温にて加熱し、低度のゲル化を行わせ
る消しゴムが開示されており、その成形温度は大体12
5〜135℃が好適であるとしている。 【0003】 【発明が解決しようとする課題】上述の如く、筆跡を消
去することだけから云えば消し屑がまとまる必要はな
い。しかし、消しゴムの性能を評価する場合、消し屑が
まとまることは消しゴムにとって大変有利なことであ
る。即ち、消し屑が紙面の消去したい部分に散らばると
消去したい筆跡を覆って消去状況が分からず、しかも、
筆跡を巻き込んで黒くなった消し屑が紙面を覆うと紙面
が汚れたように見えてしまい消去性が悪いと判断されて
しまう。消し屑がまとまる場合でも、一旦細かい消し屑
として生成した後、紙と消しゴムの間に挟まれて消しゴ
ムと紙面の擦過運動により消し屑同士がより合わされて
まとまる場合には、消し屑がまとまるまでに必要な消去
回数が多く、1、2文字を消すような場合には消し屑の
まとまりが悪い。また、一旦より合わされた消し屑のよ
りがほどけて元のバラバラの消し屑になったりしてしま
う。散らばった消し屑は回収が面倒で、消し屑で机上や
床を汚してしまう。消し屑の回収が簡単で、捨てやすく
するためには、消し屑が少ない消去回数の時でも1つに
まとまっていることが好ましい。そこで、摩耗の初めか
ら消し屑同士が練り合わされるようにして1つの消し屑
として生成すればよい。即ち、本発明が解決しようとす
る課題は、消し屑が摩耗の初めから消し屑同士が練り合
わされるようにして1つの消し屑として生成することに
より、ごく少ない擦過回数でも消し屑のまとまりがよい
消しゴムを得ることである。 【0004】 【課題を解決するための手段】本発明は、表面弾性が3
00〜420g/mmであり、表面強度が700〜13
00gであることを特徴とする消しゴムを要旨とするも
のである。 【0005】以下、詳述する。本発明に係る消しゴム
は、従来消しゴムの材料として使用されているものを用
いることができる。即ち、基材樹脂として塩化ビニル樹
脂、塩化ビニル−酢酸ビニル共重合体や、この塩化ビニ
ル樹脂と他の樹脂とを併用してなる塩化ビニル系消しゴ
ムでも、ポリオレフィン系熱可塑性エラストマ−やポリ
スチレン系熱可塑性エラストマ−を使用してなるエラス
トマ−・合成ゴム系消しゴムでもよい。上記基材樹脂以
外の成分についても、従来消しゴムの材料として使用さ
れているものを用いることができる。即ち、塩化ビニル
系消しゴムの場合、可塑剤や充填材などを用い、エラス
トマ−・合成ゴム系消しゴムの場合、充填材や軟化剤な
どを適宜選択して用いればよい。 【0006】本発明においては、消しゴムの表面弾性が
300〜420g/mmであり、表面強度が700〜1
300gであることが必要である。ここで、表面弾性と
は、消しゴム表面に直径3.0mmの円盤を一定速度2
mm/分で押し込んだとき、円盤が受ける押し込んだ長
さ当りの抵抗荷重をいう。また、表面強度とは、消しゴ
ム表面に直径3.0mmの円盤を一定速度2mm/分で
押し込んだとき、消しゴム表面が破壊したときに円盤が
受ける抵抗荷重をいう。消しゴムに円盤を押し込む場
合、消しゴム表面と円盤の平面が平行になるように配置
して、円盤を消しゴム表面に垂直に一定速度2mm/分
で押し込む。初め、円盤に押されて消しゴム表面は凹
み、円盤には反発力がかかる。この反発力は円盤が押し
込まれた長さに比例して大きくなるため、長さ当たりの
抵抗荷重として測定される。消しゴムに円盤を押し込ん
でいくと、ある時点で消しゴム表面が破壊され、円盤の
押し込んでいる部分に穴が開く。この時、円盤にかかる
反発力は最大値を示し、この値を消しゴム表面が破壊し
たときに円盤が受ける抵抗荷重とする。この場合、力を
受けるのは消しゴム表面であるため、測定される値は、
消しゴム全体の物性ではなく、表面の物性である。 【0007】表面弾性及び表面強度を測定するに当り、
円盤を用いているのは、特に表面強度の測定において、
押し込む部材の外周部が消しゴムに均一に作用する様に
なすためである。円盤の大きさは、表面弾性及び表面強
度の値に大きく影響する。そこで、円盤の大きさは、測
定対象である消しゴム表面の大きさに比べ、充分に小さ
いことが必要である。例えば消しゴム表面の大きさより
円盤の大きさが大きければ消しゴム表面の破壊が起き
ず、消しゴム全体が破壊することになる。消しゴム表面
の大きさの影響を受けずに測定するための消しゴムの大
きさは少なくとも円盤の直径の3倍以上の直径の円より
大きいことが必要と考えられる。 【0008】また、測定される消しゴムの厚さは、破壊
が起きたときに円盤が押し込んだ深さの2倍以上が必要
と考えられる。消しゴムの厚さが薄すぎると消しゴム表
面の破壊でなく、消しゴム全体の破壊となってしまうた
めである。 【0009】上記の点及び実際に使用される消しゴムの
大きさには限界があることから測定に使用する円盤の大
きさを直径3.0mmとした。円盤の厚さは、測定結果
に関係しない。表面弾性及び表面強度の測定は、できる
だけ静的な状態で測定することが必要であるが、本発明
において、円盤を消しゴム表面に押し込む速さは、2m
m/分とした。 【0010】測定される反発力は荷重表示のため、表面
弾性が300〜420g/mmであり、表面強度が80
0〜1300gであることとしたが、力の単位で表せば
表面弾性は2.9〜4.1N/mmであり、表面強度は
7.8〜12.7Nであること勿論である。 【0011】消しゴムの表面弾性及び表面強度は、成形
条件的には成形温度、加熱時間、成形時の剪断力と圧力
などが挙げられ、組成的には樹脂の種類、重合度、可塑
剤の種類、樹脂と可塑剤との比率、充填剤の種類と量な
どが挙げられる。そして、本発明の消しゴムを得るため
には、これらの条件を適宜組み合わせることによって達
成する。例えば、塩化ビニル系消しゴムに於いては、液
状の可塑剤と粉末状の塩化ビニル樹脂とを混合したペー
スト状のプラスチゾルを加熱すると、塩化ビニル樹脂が
可塑剤を吸収して膨潤する。膨潤が更に進むと塩化ビニ
ル樹脂粒子の表面が溶解しだして、冷却後は溶解した部
分で塩化ビニル樹脂粒子同士が強く結合する。この時、
塩化ビニル樹脂粒子表面の溶解による結合の度合いが強
いほど消しゴムの表面強度が大きくなるものであり、表
面弾性もある程度大きくなる。塩化ビニル樹脂粒子表面
を溶解させ、表面弾性、表面強度を大きくする方法とし
ては、加熱温度を高くする、可塑剤量/塩化ビニル樹脂
量を少なくする、塩化ビニル樹脂への吸収されやすい可
塑剤を使用する等があり、さらには加熱時に剪断力や圧
力を加える等がある。このほか、添加する充填剤量が増
えると、塩化ビニル樹脂同士の結合を阻害し、表面弾性
が大きくなる。これらのことは傾向としていえること
で、配合する材料によって表面弾性を300〜420g
/mm、表面強度を800〜1300gにするための配
合比や成形条件は異なるものである。この様に、多くの
要因の総合結果として消し屑が1つにまとまる度合いが
決まる。消し屑がねり合わされるように一つにまとまる
ことを妨げる力である、可塑剤を吸収して膨潤した塩化
ビニル樹脂粒子同士の結合力の強さは、表面強度だけで
あらわすことが出来ず、表面弾性と表面強度の2つの物
性によってあらわされる。このため、同時に表面弾性お
よび表面強度の2つの物性を制御することによって消し
屑を1つにまとめることができるものである。 【0012】そして、表面弾性が300g/mm未満や
表面強度が800g未満では消しゴムが脆くて大きな消
し屑がいくつもできる為消し屑が1つにまとまりにくい
ものである。また、表面弾性が420g/mmより大き
かったり、表面強度が1300gより大きい場合には、
消し屑が練り合わされるようにならず、より合わされる
ようになるため少ない消去回数で消し屑が一つにまとま
らないものである。 【0013】 【作用】何故に、消しゴムの表面弾性が300〜420
g/mmであり、表面強度が800〜1300gである
とき、消し屑が摩耗の初めから消し屑同士が練り合わさ
れるようにして1つの消し屑として生成し、ごく少ない
消去回数でも消し屑が1つにまとまっているかは、定か
ではないが以下のように推考される。消し屑が練り合わ
されるようになるためには、消しゴム表面から摩耗した
摩耗粉どうしが消しゴムと紙との間で擦過運動により剪
断力を受けるとき、摩耗粉中の基材樹脂粒子同士の結合
力が弱く、基材樹脂粒子が単独で移動することが必要で
ある。基材樹脂粒子同士の結合が強いと剪断力を受けて
も1つの摩耗粉としての形をとどめるため、消し屑は摩
耗粉どうしが剪断力によってよられた形でまとまる。 【0014】 【実施例】以下、本発明を実施例に基づき更に詳細に説
明する。尚、以下の実施例、比較例により得た消しゴム
について、消し屑のまとまり性を評価したが、この消し
屑のまとまり性を評価する方法として、下記の方法を用
いた。通常消しゴムを使用するように紙面上を距離5c
m4回往復する。このとき生成する消し屑の内一番大き
な消し屑の塊の重量をAとする。消去前と消去後の消し
ゴムの重量差をBとする。消し屑のまとまり性をCとす
ると、C=(A/B)×100%とした。そして、C≧
80%のとき、見た目に消し屑が一つにまとまってい
た。上記測定方法において、4回往復を1回だけでは
A,Bの重量ともに微小で測定誤差が大きいため実際に
は数十回繰返し行い、その累計のA,B重量より消し屑
のまとまり性Cを算出した。 【0015】(ポリ塩化ビニル樹脂と可塑剤との配合比
率を変えて表面弾性、表面強度を変化させた例) 実施例1 塩化ビニル樹脂(ゼオン121:重合度1600:日本ゼオン(株)製) 100重量部 可塑剤(ジイソノニルフタレート、以下DINPと略す) 160重量部 安定剤(エポキシ化大豆油) 1重量部 重質炭酸カルシウム 35重量部 上記成分を混合脱泡してプラスチゾルを得、これを深さ
12mm、幅23×63mmの容器に充填して、加熱プ
レス機にて123℃、20分間加熱成形して消しゴムを
得た。 【0016】実施例2 塩化ビニル樹脂(ゼオン121) 100重量部 可塑剤(DINP) 148重量部 安定剤(エポキシ化大豆油) 1重量部 重質炭酸カルシウム 33重量部 上記成分を実施例1と同じ方法で成形して消しゴムを得
た。 【0017】比較例1 塩化ビニル樹脂(ゼオン121) 100重量部 可塑剤(DINP) 136重量部 安定剤(エポキシ化大豆油) 1重量部 重質炭酸カルシウム 32重量部 上記成分物質を実施例1と同じ方法で成形して消しゴム
を得た。 【0018】比較例2 塩化ビニル樹脂(ゼオン121) 100重量部 可塑剤(DINP) 126重量部 安定剤(エポキシ化大豆油) 1重量部 重質炭酸カルシウム 30重量部 上記成分を実施例1と同じ方法で成形して消しゴムを得
た。 【0019】実施例1、2及び比較例1、2で得た消し
ゴムの表面弾性、表面強度、消し屑のまとまり性を表1
に示す。 【0020】 【表1】 【0021】(加熱温度を変えて表面弾性、表面強度を
変化させた例) 実施例3 実施例1において、加熱成形条件を120℃、20分間
となした以外は実施例1と同様になして消しゴムを得
た。 【0022】比較例3 実施例1において、加熱成形条件を125℃、20分間
となした以外は実施例1と同様になして消しゴムを得
た。 【0023】比較例4 実施例1において、加熱成形条件を130℃、20分間
となした以外は実施例1と同様になして消しゴムを得
た。 【0024】実施例1、3及び比較例3、4で得た消し
ゴムの表面弾性、表面強度、消し屑のまとまり性を表2
に示す。 【0025】 【表2】【0026】(充填剤量を変えて表面弾性、表面強度を
変化させた例) 実施例4 塩化ビニル樹脂(ゼオン121) 100重量部 可塑剤(アデカサイザーPN−160:アジピン酸系のポリエステル可塑剤: 旭電化工業(株)製) 160重量部 安定剤(エポキシ化大豆油) 1重量部 重質炭酸カルシウム 35重量部 上記成分を混合脱泡してプラスチゾルを得、これを深さ
12mm、幅23×63mmの容器に充填して、加熱プ
レス機にて130℃、20分間加熱成形して、消しゴム
を得た。 【0027】比較例5 塩化ビニル樹脂(ゼオン121) 100重量部 可塑剤(アデカサイザーPN−160) 160重量部 安定剤(エポキシ化大豆油) 1重量部 重質炭酸カルシウム 122重量部 上記成分を実施例4と同じ方法で成形を行って消しゴム
を得た。 【0028】比較例6 塩化ビニル樹脂(ゼオン121) 100重量部 可塑剤(アデカサイザーPN−160) 180重量部 安定剤(エポキシ化大豆油) 1重量部 重質炭酸カルシウム 38重量部 上記成分を実施例4と同じ方法で成形を行って消しゴム
を得た。 【0029】実施例5 塩化ビニル樹脂(ゼオン121) 100重量部 可塑剤兼安定剤(エポキシ化大豆油) 160重量部 重質炭酸カルシウム 35重量部 上記成分を実施例4と同じ方法で成形を行って消しゴム
を得た。 【0030】実施例6 塩化ビニル樹脂(ゼオン121) 100重量部 可塑剤兼安定剤(エポキシ化大豆油) 160重量部 重質炭酸カルシウム 122重量部 上記成分を実施例4と同じ方法で成形を行って消しゴム
を得た。 【0031】実施例4〜6及び比較例5、6で得た消し
ゴムの表面弾性、表面強度、消し屑のまとまり性を表3
に示す。 【0032】 【表3】【0033】(重合度の大きい塩化ビニル樹脂を使用し
て表面弾性、表面強度を変化させた例) 実施例7 塩化ビニル樹脂(ゼオン43H:重合度3500:日本ゼオン(株)製) 100重量部 可塑剤(DINP) 160重量部 安定剤(エポキシ化大豆油) 1重量部 重質炭酸カルシウム 35重量部 上記成分を実施例4と同じ方法で成形を行って消しゴム
を得た。 【0034】比較例7 実施例7において加熱成形条件を140℃、20分間と
なした以外は実施例7と同様になして消しゴムを得た。 【0035】比較例8 塩化ビニル樹脂(ゼオン43H) 100重量部 可塑剤(DINP) 160重量部 安定剤(エポキシ化大豆油) 1重量部 重質炭酸カルシウム 122重量部 上記成分を実施例4と同じ方法で成形を行って消しゴム
を得た。 【0036】実施例7及び比較例7、8で得た消しゴム
の表面弾性、表面強度、消し屑のまとまり性を表4に示
す。 【0037】 【表4】 【0038】実施例8〜10、比較例9 塩化ビニル樹脂(ゼオン121) 100重量部 可塑剤(DINP) 160重量部 安定剤(エポキシ化大豆油) 1重量部 重質炭酸カルシウム 35重量部 上記成分の混合物をシリンダー径65mmの押出成形
機、圧縮比3のスクリューを使用して押出成形を行って
消しゴムを得た。押出成形機各部分の温度は、表5の通
りとした。 【0039】 【表5】【0040】実施例8〜10及び比較例9で得た消しゴ
ムの表面弾性、表面強度、消し屑のまとまり性を表6に
示す。 【0041】 【表6】 【0042】 【発明の効果】以上、詳細に説明したように、表面弾性
が300〜420g/mmであり、表面強度が800〜
1300gである消しゴムは少ない擦過回数で消し屑の
殆どが1つの塊にまとまるものである。
Description: BACKGROUND OF THE INVENTION [0001] 1. Field of the Invention [0002] The present invention relates to an eraser for erasing handwriting of a pencil, a mechanical pencil or the like. About the eraser united into one. 2. Description of the Related Art Conventionally, erasers have been known as vinyl chloride resins using a vinyl chloride resin or a copolymer of vinyl chloride as a base resin, natural rubber resins mainly using natural rubber, and thermal rubbers. Elastomer using plastic elastomer or synthetic rubber
-Synthetic rubber type is known. Eraser with vinyl chloride resin as base resin, vinyl chloride resin and plasticizer,
It is made by heating a paste-like plastisol mixed with fillers and other additives as needed to cause the vinyl chloride resin to absorb the plasticizer. Erasers using natural rubber as a base resin are produced by mixing natural rubber with sub and filler materials and vulcanizing them. An eraser using a thermoplastic elastomer or a synthetic rubber as a base resin is prepared by mixing a thermoplastic elastomer or a synthetic rubber, a filler, and, if necessary, a softener, and then heat-molding the mixture in an unvulcanized state. Incidentally, the eraser needs to be worn by rubbing against the paper surface. This is for the following reason. The handwriting of a pencil or mechanical pencil is obtained by attaching powder of a pencil or mechanical pencil core worn by rubbing with paper to the paper surface. The abrasion powder of the core is removed from the paper surface by re-adhering to the surface of the eraser rubber or the surface of the eraser, and the handwriting is erased. At this time, if the eraser is worn and no eraser dust is generated, the eraser surface is covered with the core abrasion powder, the core abrasion powder cannot be attached any more, and the handwriting cannot be further erased. Not only that, the abrasion powder of the core once adhered to the eraser adheres to the paper again, causing the paper to become dirty.
For this reason, it is necessary that the eraser be worn out by rubbing with paper and produce eraser dust. In order to obtain such characteristics, for example, a vinyl chloride-based eraser is molded at a lower heating temperature than a normal vinyl chloride resin molded product. This is known from Japanese Patent Publication No. 32-8220. That is, Japanese Patent Publication No. 32-8220 discloses an eraser in which a plasticizer is added in an amount of 80 to 160% by weight of a vinyl chloride resin and heated at a relatively low temperature to cause a low degree of gelation. It is disclosed that the molding temperature is about 12
It is stated that a temperature of 5 to 135 ° C. is suitable. [0003] As described above, there is no need to collect erased scraps simply because the handwriting is erased. However, when the performance of an eraser is evaluated, it is very advantageous for the eraser that the eraser is collected. That is, if the erased dust is scattered on the portion of the paper to be erased, the handwriting to be erased is covered and the erasing status is unknown, and
If the erased dust that has become black due to the involvement of the handwriting covers the paper surface, the paper surface looks dirty, and the erasability is determined to be poor. Even when erased dust is collected, once it is generated as fine erased dust, if the erased dust is sandwiched between paper and eraser and the eraser and the paper are rubbed together, the erased dust is gathered together. If the number of necessary erasures is large and one or two characters are to be erased, the erasable dust is not well organized. In addition, the scraps that have been combined once become loose and become the original scraps. Scattered scraps are cumbersome to collect and stain desks and floors with the scraps. In order to make it easy to collect and erase the scraps, it is preferable that the scraps are united even when the number of erases is small. Therefore, it is sufficient to form the erased scraps as one erased scrap by kneading the erased scraps from the beginning of wear. That is, the problem to be solved by the present invention is that the erased dust is kneaded together from the beginning of wear and is generated as one erased dust, so that the erased dust can be gathered even with a very small number of rubs. Getting an eraser. SUMMARY OF THE INVENTION The present invention provides a method for manufacturing a semiconductor device having a surface elasticity of 3
00 to 420 g / mm and a surface strength of 700 to 13
The grit is an eraser characterized by being 00 g. The details will be described below. As the eraser according to the present invention, those conventionally used as a material for the eraser can be used. That is, even if a vinyl chloride resin, a vinyl chloride-vinyl acetate copolymer, or a vinyl chloride-based eraser obtained by using this vinyl chloride resin in combination with another resin is used as a base resin, a polyolefin-based thermoplastic elastomer or a polystyrene-based thermosetting rubber can be used. An elastomer using a plastic elastomer, or a synthetic rubber-based eraser may be used. As the components other than the base resin, those conventionally used as the material of the eraser can be used. That is, in the case of a vinyl chloride-based eraser, a plasticizer or a filler may be used, and in the case of an elastomer / synthetic rubber-based eraser, a filler or a softener may be appropriately selected and used. In the present invention, the eraser has a surface elasticity of 300 to 420 g / mm and a surface strength of 700 to 1
It needs to be 300 g. Here, the surface elasticity means that a disk having a diameter of 3.0 mm is applied to the eraser surface at a constant speed of 2.
When the disk is pushed at a rate of mm / min, it refers to the resistive load per unit length of the pushed disk. The term "surface strength" refers to a resistance load applied to a disk when a disk having a diameter of 3.0 mm is pushed into the surface of the eraser at a constant speed of 2 mm / min and the surface of the eraser is broken. When the disk is pushed into the eraser, the disk is arranged so that the surface of the eraser and the plane of the disk are parallel to each other, and the disk is pushed perpendicular to the surface of the eraser at a constant speed of 2 mm / min. At first, the surface of the eraser is depressed by being pushed by the disk, and a repulsive force is applied to the disk. Since this repulsive force increases in proportion to the length of the pressed disk, it is measured as a resistance load per length. As the disk is pushed into the eraser, the surface of the eraser is destroyed at some point, and a hole is opened in the pressed part of the disk. At this time, the repulsive force applied to the disk shows a maximum value, and this value is defined as the resistance load applied to the disk when the rubber surface is broken. In this case, the force measured is the eraser surface, so the measured value is
It is not the physical properties of the entire eraser, but the physical properties of the surface. In measuring surface elasticity and surface strength,
The use of a disk is particularly important for measuring surface strength.
This is because the outer peripheral portion of the member to be pushed acts uniformly on the eraser. The size of the disk greatly affects the values of surface elasticity and surface strength. Therefore, the size of the disk needs to be sufficiently smaller than the size of the eraser surface to be measured. For example, if the size of the disk is larger than the size of the eraser surface, the eraser surface will not be destroyed, and the entire eraser will be destroyed. It is considered necessary that the size of the eraser to be measured without being affected by the size of the eraser surface is larger than a circle having a diameter of at least three times the diameter of the disk. Further, it is considered that the thickness of the eraser to be measured is required to be at least twice the depth of the disk pressed when the breakage occurs. If the thickness of the eraser is too small, the entire eraser is destroyed, not the surface of the eraser. Since the above point and the size of the eraser actually used are limited, the size of the disk used for the measurement was set to 3.0 mm in diameter. The thickness of the disk is not relevant for the measurement result. It is necessary to measure the surface elasticity and the surface strength in a state as static as possible. In the present invention, the speed at which the disk is pushed into the eraser surface is 2 m.
m / min. [0010] The measured repulsive force has a surface elasticity of 300 to 420 g / mm and a surface strength of 80
Although it is assumed that the weight is 0 to 1300 g, the surface elasticity is 2.9 to 4.1 N / mm and the surface strength is 7.8 to 12.7 N in terms of force. The surface elasticity and surface strength of the eraser include molding temperature, heating time, shear force and pressure during molding in terms of molding conditions, and in terms of composition, the type of resin, the degree of polymerization, and the type of plasticizer. , The ratio between the resin and the plasticizer, and the type and amount of the filler. And, in order to obtain the eraser of the present invention, it is achieved by appropriately combining these conditions. For example, in the case of a vinyl chloride-based eraser, when a paste-like plastisol obtained by mixing a liquid plasticizer and a powdery vinyl chloride resin is heated, the vinyl chloride resin absorbs the plasticizer and swells. As the swelling proceeds further, the surfaces of the vinyl chloride resin particles begin to dissolve, and after cooling, the vinyl chloride resin particles are strongly bonded to each other at the dissolved portion. At this time,
The stronger the degree of bonding due to dissolution of the surface of the vinyl chloride resin particles, the greater the surface strength of the eraser, and the surface elasticity also increases to some extent. Methods for increasing the surface elasticity and surface strength by dissolving the surface of the vinyl chloride resin particles include increasing the heating temperature, reducing the amount of plasticizer / vinyl chloride resin, and using a plasticizer that is easily absorbed by the vinyl chloride resin. And a shear force or a pressure applied during heating. In addition, when the amount of the filler to be added increases, the bonding between the vinyl chloride resins is inhibited, and the surface elasticity increases. These facts can be said to be trends, and the surface elasticity is 300 to 420 g depending on the material to be blended.
/ Mm, the compounding ratio and molding conditions for making the surface strength 800 to 1300 g are different. In this way, the degree to which erased dust is united as one is determined as an overall result of many factors. The strength of the bonding force between the vinyl chloride resin particles that have swollen by absorbing the plasticizer, which is the force that prevents the eraser dust from sticking together as a result of being stuck, cannot be expressed only by surface strength, It is represented by two physical properties, surface elasticity and surface strength. Therefore, by simultaneously controlling the two physical properties of the surface elasticity and the surface strength, it is possible to combine erased scraps into one. If the surface elasticity is less than 300 g / mm or the surface strength is less than 800 g, the eraser is brittle and a number of large erases can be formed. When the surface elasticity is larger than 420 g / mm or the surface strength is larger than 1300 g,
The erased chips are not kneaded, but are more closely combined, so that the erased scraps are not united with a small number of erasures. The reason why the surface elasticity of the eraser is 300 to 420
g / mm and a surface strength of 800 to 1300 g, erased dust is generated as one erased dust by knitting the erased dust together from the beginning of abrasion. It is not clear whether they are united, but it is presumed as follows. In order for the eraser dust to be kneaded, when the abrasion powder worn from the eraser surface is subjected to a shearing force due to the rubbing motion between the eraser and the paper, the bonding force between the base resin particles in the abrasion powder is increased. And the base resin particles need to move alone. If the bonding between the base resin particles is strong, even if it is subjected to a shearing force, the shape of the abrasion powder remains as one abrasion powder, so that the eraser dust is collected in a form in which the abrasion powders are caused by the shearing force. Hereinafter, the present invention will be described in more detail with reference to examples. The eraser obtained in the following Examples and Comparative Examples was evaluated for the unity of erased dust. The following method was used to evaluate the unity of the erased dust. Distance 5c on paper like using normal eraser
m4 reciprocations. Let A be the weight of the largest erased lump mass generated at this time. Let B be the weight difference between the eraser before and after erasing. Assuming that the cohesiveness of the erased dust is C, C = (A / B) × 100%. And C ≧
At 80%, the eraser was apparently united in one. In the above-described measurement method, if the four reciprocations are performed only once, the weights of A and B are very small and the measurement error is large. Therefore, the measurement is actually repeated several tens of times, and the cohesiveness C of the erased dust is determined from the total A and B weights. Calculated. (Example of changing surface elasticity and surface strength by changing the blending ratio of polyvinyl chloride resin and plasticizer) Example 1 Vinyl chloride resin (Zeon 121: polymerization degree 1600: manufactured by Zeon Corporation) 100 parts by weight Plasticizer (diisononyl phthalate, hereinafter abbreviated as DINP) 160 parts by weight Stabilizer (epoxidized soybean oil) 1 part by weight Heavy calcium carbonate 35 parts by weight The above components are mixed and defoamed to obtain a plastisol. The container was filled into a container having a length of 12 mm and a width of 23 × 63 mm, and was heated and molded by a heating press machine at 123 ° C. for 20 minutes to obtain an eraser. Example 2 100 parts by weight of vinyl chloride resin (Zeon 121) 148 parts by weight of plasticizer (DINP) 1 part by weight of stabilizer (epoxidized soybean oil) 33 parts by weight of heavy calcium carbonate The above components were the same as in Example 1. Molded by the method to obtain an eraser. Comparative Example 1 100 parts by weight of vinyl chloride resin (Zeon 121) 136 parts by weight of plasticizer (DINP) 1 part by weight of stabilizer (epoxidized soybean oil) 32 parts by weight of heavy calcium carbonate Molding was performed in the same manner to obtain an eraser. Comparative Example 2 Vinyl chloride resin (Zeon 121) 100 parts by weight Plasticizer (DINP) 126 parts by weight Stabilizer (epoxidized soybean oil) 1 part by weight Heavy calcium carbonate 30 parts by weight The above components were the same as in Example 1. Molded by the method to obtain an eraser. Table 1 shows the surface elasticity, surface strength and unity of erased scraps of the erasers obtained in Examples 1 and 2 and Comparative Examples 1 and 2.
Shown in [Table 1] (Example in which surface elasticity and surface strength are changed by changing heating temperature) Example 3 In Example 1, the same procedure as in Example 1 was carried out except that the heat molding conditions were 120 ° C. and 20 minutes. I got an eraser. Comparative Example 3 An eraser was obtained in the same manner as in Example 1 except that the heat molding conditions were changed to 125 ° C. and 20 minutes. Comparative Example 4 An eraser was obtained in the same manner as in Example 1 except that the heat molding conditions were changed to 130 ° C. and 20 minutes. Table 2 shows the surface elasticity, surface strength, and unity of erased dust of the erasers obtained in Examples 1 and 3 and Comparative Examples 3 and 4.
Shown in [Table 2] (Example of changing surface elasticity and surface strength by changing the amount of filler) Example 4 100 parts by weight of vinyl chloride resin (Zeon 121) Plasticizer (Adecaizer PN-160: adipic acid-based polyester plasticizer) : Asahi Denka Kogyo Co., Ltd.) 160 parts by weight Stabilizer (epoxidized soybean oil) 1 part by weight Heavy calcium carbonate 35 parts by weight The above components were mixed and defoamed to obtain a plastisol, which was 12 mm in depth and 23 in width. The resultant was filled in a container having a size of × 63 mm, and was molded by heating at 130 ° C. for 20 minutes using a heating press to obtain an eraser. Comparative Example 5 Vinyl chloride resin (Zeon 121) 100 parts by weight Plasticizer (ADEKA SIZER PN-160) 160 parts by weight Stabilizer (epoxidized soybean oil) 1 part by weight Heavy calcium carbonate 122 parts by weight Molding was performed in the same manner as in Example 4 to obtain an eraser. Comparative Example 6 100 parts by weight of vinyl chloride resin (Zeon 121) 180 parts by weight of plasticizer (Adekasizer PN-160) 1 part by weight of stabilizer (epoxidized soybean oil) 1 part by weight 38 parts by weight of heavy calcium carbonate Molding was performed in the same manner as in Example 4 to obtain an eraser. Example 5 Vinyl chloride resin (Zeon 121) 100 parts by weight Plasticizer and stabilizer (epoxidized soybean oil) 160 parts by weight Heavy calcium carbonate 35 parts by weight The above components were molded in the same manner as in Example 4. I got an eraser. Example 6 Vinyl chloride resin (Zeon 121) 100 parts by weight Plasticizer and stabilizer (epoxidized soybean oil) 160 parts by weight Heavy calcium carbonate 122 parts by weight The above components were molded in the same manner as in Example 4. I got an eraser. Table 3 shows the surface elasticity, surface strength, and unity of erased scraps of the erasers obtained in Examples 4 to 6 and Comparative Examples 5 and 6.
Shown in [Table 3] (Example in which surface elasticity and surface strength were changed by using a vinyl chloride resin having a high degree of polymerization) Example 7 100 parts by weight of vinyl chloride resin (Zeon 43H: Degree of polymerization 3500: manufactured by Zeon Corporation) Plasticizer (DINP) 160 parts by weight Stabilizer (epoxidized soybean oil) 1 part by weight Heavy calcium carbonate 35 parts by weight The above components were molded in the same manner as in Example 4 to obtain an eraser. Comparative Example 7 An eraser was obtained in the same manner as in Example 7, except that the heat molding conditions were changed to 140 ° C. and 20 minutes. Comparative Example 8 Vinyl chloride resin (Zeon 43H) 100 parts by weight Plasticizer (DINP) 160 parts by weight Stabilizer (epoxidized soybean oil) 1 part by weight Heavy calcium carbonate 122 parts by weight The above components were the same as in Example 4. Molding was performed by the method to obtain an eraser. Table 4 shows the surface elasticity, surface strength and unitedness of erased scraps of the erasers obtained in Example 7 and Comparative Examples 7 and 8. [Table 4] Examples 8-10, Comparative Example 9 100 parts by weight of vinyl chloride resin (Zeon 121) 160 parts by weight of plasticizer (DINP) 1 part by weight of stabilizer (epoxidized soybean oil) 35 parts by weight of heavy calcium carbonate Was extruded using an extruder having a cylinder diameter of 65 mm and a screw having a compression ratio of 3 to obtain an eraser. Table 5 shows the temperature of each part of the extruder. [Table 5] Table 6 shows the surface elasticity, surface strength, and unity of erased scraps of the erasers obtained in Examples 8 to 10 and Comparative Example 9. [Table 6] As described above, the surface elasticity is 300 to 420 g / mm and the surface strength is 800 to
An eraser weighing 1300 g is one in which most of the erased waste is collected in one lump with a small number of times of rubbing.

Claims (1)

(57)【特許請求の範囲】 【請求項1】 表面弾性が300〜420g/mmであ
り、表面強度が700〜1300gであることを特徴と
する消しゴム。
(57) Claims 1. An eraser having a surface elasticity of 300 to 420 g / mm and a surface strength of 700 to 1300 g.
JP25474795A 1995-09-06 1995-09-06 eraser Expired - Fee Related JP3438433B2 (en)

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JP4068402B2 (en) * 2001-10-26 2008-03-26 株式会社トッパンTdkレーベル Scratch card
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