JPS615998A - Eraser having thermoplastic substance and manufacture thereof - Google Patents

Eraser having thermoplastic substance and manufacture thereof

Info

Publication number
JPS615998A
JPS615998A JP60034716A JP3471685A JPS615998A JP S615998 A JPS615998 A JP S615998A JP 60034716 A JP60034716 A JP 60034716A JP 3471685 A JP3471685 A JP 3471685A JP S615998 A JPS615998 A JP S615998A
Authority
JP
Japan
Prior art keywords
eraser
rubber
eraser according
thermoplastic
ethylene
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.)
Granted
Application number
JP60034716A
Other languages
Japanese (ja)
Other versions
JPH0773958B2 (en
Inventor
ヴエルナー・ハントル
ジイルヴイア・ヴアツル
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.)
JS Staedtler GmbH and Co KG
Original Assignee
JS Staedtler GmbH and Co KG
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 JS Staedtler GmbH and Co KG filed Critical JS Staedtler GmbH and Co KG
Publication of JPS615998A publication Critical patent/JPS615998A/en
Publication of JPH0773958B2 publication Critical patent/JPH0773958B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B43WRITING OR DRAWING IMPLEMENTS; BUREAU ACCESSORIES
    • B43LARTICLES FOR WRITING OR DRAWING UPON; WRITING OR DRAWING AIDS; ACCESSORIES FOR WRITING OR DRAWING
    • B43L19/00Erasers, rubbers, or erasing devices; Holders therefor
    • B43L19/0025Eraser or rubber material, e.g. comprising hard particles
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24Acids; Salts thereof
    • C08K3/26Carbonates; Bicarbonates
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0016Plasticisers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0025Crosslinking or vulcanising agents; including accelerators
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/16Elastomeric ethene-propene or ethene-propene-diene copolymers, e.g. EPR and EPDM rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L53/02Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L65/00Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
    • C08L65/02Polyphenylenes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/04Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、熱可塑性物質が;P■ノλレソイ7J重合体
である、熱可塑性物質なイJする消し一1゛7、並ひに
その製法シこ関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a thermoplastic material, the thermoplastic material being a P.lambda. It's about Shiko.

従来の技術 西独国特許出願公開第3043941号明細遊には、特
に、エチレン及び/又は(α−)オレフィンの重合によ
って製造した、僅かに結晶化可能なポリオレフィングラ
フト共重合体エラストマーを含有するような消しゴムが
記載されている。このエラストマーはファクチス、充填
剤及び顔料と混合されて消しゴムに加工される。
Prior Art DE 30 43 941 discloses, inter alia, such polymers containing slightly crystallizable polyolefin graft copolymer elastomers prepared by polymerization of ethylene and/or (α-)olefins. An eraser is listed. This elastomer is mixed with factice, fillers and pigments and processed into erasers.

その他に補足的に、上記混合物に特にエチレン/プロピ
レン三元共重合体をベースとするゴム、場合により捷1
こエチレン/プロピレン/ジエン王元共重合体を添加す
ることもできる。
In addition, the above mixture may be added in particular to a rubber based on an ethylene/propylene terpolymer, optionally with
An ethylene/propylene/diene copolymer may also be added.

しかしながら、この種の消しゴムは、この場合必須成分
であるファクチスに基づき、著しくに化不安定性である
。史て、この場合の消しゴムは軟化剤を含有しない、従
って基礎拐刺の稠度が任意に調整可能できない。それに
より、こ才1らの材料をあらゆる常用の消しゴム用の製
造装置を用いて加工することは不可能である。更に、こ
の場合には完成した消しゴムの硬度は比較的狭い限界内
だけで変動されうるにすぎな(・発明が解決しようとす
る問題点 従って、本発明の課題は、前記欠点を有せず、従って極
めて老化不安定性であり、良好jC摩耗特性を有し7、
広範囲内で可変の硬度調整が用能でありかつあらゆる従
来の製造装置で製造−することができる消しゴムを提供
することである問題点を解決する1こめの手段 KJ記課題は、特許請求の範囲の独立a^求項に記載の
特徴によシ特に簡単に解決さねイ、。特殊な態様及び詳
細並びに有利な方θ、は、肪¥f )i?+ A<の範
囲第2項以下に記載されて℃・ろ。
However, erasers of this type are extremely chemically unstable due to the factice, which is an essential component in this case. Historically, the eraser in this case does not contain a softening agent, so the consistency of the base ablation cannot be adjusted arbitrarily. As a result, it is not possible to process these materials using any conventional eraser manufacturing equipment. Moreover, in this case the hardness of the finished eraser can only be varied within relatively narrow limits. Therefore, it is extremely aging unstable and has good JC wear characteristics7.
One means of solving the problem is to provide an eraser which is capable of variable hardness adjustment within a wide range and which can be manufactured on any conventional manufacturing equipment. This is not particularly easy to solve due to the characteristics described in the independent a^ requirement. Special aspects and details and advantages θ, is fat¥f)i? + A < range as described in Section 2 below.

作用 完全に架橋しfこゴムを包埋し−〔、′;有すイ、執I
I:塑性オレフィンをベースとす<:1合成成分:j、
消しゴムを製造するため(・τ極めて適当てあ<1.こ
yが立証された。このf手の消しゴムはあらゆ、z、 
+9i望tノ)特?iI’v楢しかつ更に簡単かつ廉価
に製造可能である。
Function Completely crosslinks and embeds the rubber.
I: Based on plastic olefin <:1 Synthetic component: j,
In order to manufacture erasers, it has been proven that (・τ extremely suitable <1.
+9i desired no) special? iI'v and can be manufactured more easily and inexpensively.

本発明で使用する合成成分及びその製法は、例えば米国
特許第4130535号明細書から既:こ数年来自体公
知である。しかし、該明細書VC[H4′/J<されf
こ混合物は特に熱可塑性特性を有する硬質の加硫した生
成物を製造する1こめに提案されて℃・るので、該開示
から直ちに、それを用いて製造した、常に柔軟でありか
つ自体で熱可塑性である必要はない消しゴムが特に良好
な特性をイJすることは全く想到され得ないことである
The synthetic components used in the invention and their preparation have been known per se for several years, for example from US Pat. No. 4,130,535. However, in the specification VC[H4'/J<
Since this mixture has been proposed especially for producing hard vulcanized products with thermoplastic properties, from this disclosure it is immediately possible to use it to produce hard, vulcanized products that are always flexible and heat-resistant in their own right. It is completely inconceivable that an eraser, which need not be plastic, would exhibit particularly good properties.

熱白丁塑性メレフィンがその場で重合し71こエテレン
ープロビレンーノエンーモノオレフィン(略語EPDM
 )を有するポリゾロピレンでありかつゴノ・が同様に
エチレン、プロピレン及び共役して(・7cいジエンか
ら成る、すなわち同様にEPDMイ″4料から成る場合
が特に有利であることが立証さねfこ。共役していない
、ジエンは有利にはエナリテンーノルボルネンであって
よく、一方ゴムは硫黄で架橋さj−iて(・ろべき↑あ
り、イJ利には架橋度7×10 モル/rnlを有しか
つ粒度05〜2μm、有利にはlμInで看在し、てし
・ろべきである。
The hot white plastic melefin polymerizes in situ to form 71 ethylene-propylene-monoolefins (abbreviated as EPDM).
It has proved particularly advantageous if the polyzolopylene has the same ethylene, propylene and conjugated diene (. The unconjugated diene may advantageously be an enarytenorbornene, while the rubber is crosslinked with sulfur and has a degree of crosslinking of 7×10 mol/ It should have a particle size of 05 to 2 μm, preferably lμIn.

更に、別の添加物な(・しは別の結合剤、充填剤、軟化
剤又は同種のものとして、スチレ//ブメノエンブロッ
ク共1合体(SBS )、スチレン/イソプレンゴム(
SIS ) 、エチレン/ゾロピレン共及び/又は三元
共重合体(ppM)、ボlJ塩化ビニル(pvc )、
エチレンエチルアクリレート及び/又はその他のシラス
ナック、並ひに場合により、特に充填剤として、rt 
d!i (炭酸力ルンウム)、硫化亜鉛、酸化マダイ、
ブタノ1、重晶石、軽石粉、ガラス粉、ガラス粉及び/
y。
In addition, other additives such as styrene//bumenoene block comonomer (SBS), styrene/isoprene rubber (
SIS), ethylene/zolopyrene co- and/or terpolymer (ppM), VolJ vinyl chloride (PVC),
rt
d! i (carbonate), zinc sulfide, red sea bream oxide,
Butano 1, barite, pumice powder, glass powder, glass powder and/
y.

はファクチス或は11こイ1利に(よ軟化剤とし−6、
ポリブタノエン、ポリアルギルベ/セ゛)、ノ゛シフイ
ン糸もしくはナフデン糸71b−7クレー 1又はその
他のニスデル、並びに場合により力(を帰もしくは有機
顔料が染料として1)イIご引′ビr−y  (もよい
is used as a factice or as a softening agent.
Polybutanoene, polyalgylbene/naphdenoid yarn 71b-7 clay 1 or other Nisdel, and optionally organic pigments as dyes 1). good.

本弁明:Cよろ消しゴムは特1′こ簡ヰ:二:ま次のよ
う:′こして製造することができる。1す第1の独立し
た製作工程で、最初にゴムを完全に架橋させ、次いでオ
レフィン中に包埋させかつそれと一緒に重合させること
により合成成分を製造する。この場合、重合はゴムとオ
レフィン夫々自体間の1合及び更にま1こ両者の重合を
包含する。
This defense: C-cross eraser can be produced by the following method. 1. In a first separate production step, the synthetic component is prepared by first completely crosslinking the rubber and then embedding it in the olefin and copolymerizing it therewith. In this case, the polymerization includes one and even two polymerizations between the rubber and the olefin, respectively themselves.

従って、出来上った合成成分はポリオレフィンと、完全
に重合し完全に架橋したゴムから成る共′811合体で
ある。この製造工程は外部で行なわれる、すなわち本来
の消しゴム製造とは独立し、て実施することができる。
The resulting synthetic component is therefore a co'811 composite consisting of a polyolefin and a fully polymerized, fully crosslinked rubber. This production process can be carried out externally, ie independently of the actual eraser production.

場合により、この共11(合体を特別のメーカーによっ
て製造させかつ市販品として提供することもできる。
Optionally, this combination can also be manufactured by a special manufacturer and provided as a commercial product.

次いで、元来の消しゴムの製造は自体公知方法で行なう
。この際には、先に製造しfこ共重合体を合成成分とし
て全組成の別の成分と、均質(分散しTこ)な全混合物
が形成される1で混合むる。
The original eraser is then produced in a manner known per se. In this case, the previously produced copolymer is used as a synthetic component and mixed with other components of the entire composition to form a homogeneous (dispersed) total mixture.

次いで、この全混合物を常法で押出機、−射出成形機、
叛プレス乞用(・て又はその他の製i′、1j装置で用
塑化しかつ完全に又:ま部分的に成形(並びに場合によ
り引く青き徐動しかつ所望の太ききて切断又は成形する
This entire mixture is then passed through an extruder, - an injection molding machine, in a conventional manner.
It is then plasticized and completely or partially formed (and optionally cut or formed to the desired thickness) using a press or other manufacturing equipment.

実施例 次に図示の実施例につき本発明の詳細な説明する。この
場合、5記載は1量%である。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will now be described in detail with reference to the illustrated embodiments. In this case, description 5 is 1% by weight.

例1(組成範囲例) 合成成分(ポリオレフィン及び 重合L、完全に架橋したゴムから成 る共13合体)         5〜50%充填剤(
炭酸カルシウム又はその他) 30〜85% ファクチス            0〜30%その池
の添加物、特に別の献+iJ塑 性シラスチック、例えばSBS 、 SIS、  PV
Cその他           0〜30%その他の添
加物、例えば軟化剤、 安定剤、染料又はその他       ○〜コ50%夫
々特;〔適当なイ固々の)iけ特にi’9r 5i−σ
)男″求に左右されかつ主として所望の弾性、機械的強
度、剛性、硬さ、摩耗性、手ざわり及びその他の最終製
品ないしは消しゴムに対する要求によって決定される。
Example 1 (composition range example) Synthetic components (polyolefin and polymerized L, co-13 composite consisting of fully crosslinked rubber) 5-50% filler (
Calcium carbonate or other) 30-85% factice 0-30% its additives, especially other additives + iJ plastic silastics, e.g. SBS, SIS, PV
C Others 0-30% Other additives, such as softeners, stabilizers, dyes or others ○-50% each;
) depends on the user's needs and is primarily determined by the desired elasticity, mechanical strength, stiffness, hardness, abrasion, texture and other requirements for the final product or eraser.

例2(製造例1) 合成成分20%、白亜40%及びガラス粉40%をヘン
ンエルミキサー(Henschelmischer )
内で約2分間混合する。次いで、この混合物を反対方向
に回転する二重スクリュー押出機内で180〜230℃
の間の温度で可塑化しかつ場合により成形したストラン
ドに成形し、該ストランドを例えば水浴内で冷却しかつ
引続き消しゴムとして常用の大きさに切断する。
Example 2 (Production Example 1) 20% synthetic ingredients, 40% chalk and 40% glass powder were mixed in a Henschelmischer mixer.
Mix for about 2 minutes. This mixture is then heated to 180-230°C in a counter-rotating double screw extruder.
The strands are plasticized and optionally formed into shaped strands, which are cooled, for example in a water bath, and subsequently cut into the customary sizes for erasers.

例3(製造例2) 合成成分16%、スチレン/ブタジェンブロック共重合
体(SBS ) 8%、ポリアルキルベンゼン13%及
び白亜63%をハインッミキサー(Heinzmisc
her )内f高速攪拌機で混合し、摩擦熱を発生させ
る。約110℃で、材料の溶解が起る。この材料を冷却
及び造粒するために冷却混合種で35℃に調温しかつ粉
砕する。該顆粒を射出成形機で所望の消しゴム形にしか
つ離型後場合により冷却する。
Example 3 (Production Example 2) 16% of the synthetic components, 8% of styrene/butadiene block copolymer (SBS), 13% of polyalkylbenzene and 63% of chalk were mixed in a Heinzmisc mixer (Heinzmisc).
(her) Mix with a high-speed stirrer to generate frictional heat. At about 110°C, melting of the material occurs. This material is cooled and granulated by controlling the temperature to 35° C. with a cooling mixture and pulverizing it. The granules are shaped into the desired eraser shape in an injection molding machine and optionally cooled after demolding.

例牛(製造例3) 合成成分6%、SBS 8%、ポリアルキルベ/ゼン1
3.5%、白亜635%及びファクチス9%をハインツ
ミキサーで約130℃に加熱しかつその際溶解させる。
Example beef (Production example 3) Synthetic ingredients 6%, SBS 8%, Polyalkylbe/Zen 1
3.5%, chalk 635% and factice 9% are heated to approx. 130° C. in a Heinz mixer and are then dissolved.

冷却後、Kレットを押出機中100〜160℃の温度で
可塑化しかつストランド状に押出し、冷却しかつ切断し
かつ場合によりバレル仕上げする。
After cooling, the K-let is plasticized in an extruder at temperatures of 100 DEG to 160 DEG C. and extruded into strands, cooled, cut and optionally barreled.

その他の混合実施例は、以下の表に1とめて示す。Other mixing examples are listed in the table below.

本発明で使用しかつ提案しTこ合成酸物は、同時に熱可
塑性物質を形成しかつ消しゴム混合物中で結合剤、充填
剤又はその他の混合成分して作用する。
The synthetic acid used and proposed in the present invention simultaneously forms a thermoplastic and acts as a binder, filler or other mixed component in the eraser mixture.

Claims (1)

【特許請求の範囲】 1、熱可塑性物質がポリオレフィン共重合体である、熱
可塑性物質を有する消しゴムにおいて、合成成分が熱可
塑性ポリオレフィンであり、該ポリオレフィンが重合し
、完全に架橋したゴムを包埋して含有することを特徴と
する、熱可塑性物質を有する消しゴム。 2、熱可塑性オレフィンがその場で重合したエチレン/
プロピレン/ジエン/モノオレフィン(EPDM)を有
するポリプロピレンである、特許請求の範囲第1項記載
の消しゴム。 3、ゴムがエチレン、プロピレン及び少量の共役してい
ないジエンから成る、特許請求の範囲第1項又は第2項
記載の消しゴム。 4、共役していないジエンがエチリデン−ノルボルネン
である、特許請求の範囲第3項記載の消しゴム。 5、ゴムが硫黄架橋系で架橋されている、特許請求の範
囲第1項から第4項までのいずれか1項記載の消しゴム
。 6、ゴムの架橋度が7×10^−^5モル/lよりも大
きい、特許請求の範囲第5項記載の消しゴム。 7、ゴムが0.5〜2μmの粒度を有する、特許請求の
範囲第1項から第6項までのいずれか1項記載の消しゴ
ム。 8、別の添加物として、スチレン/ブタジエンブロック
共重合体、スチレン/イソプレンゴム、エチレン/プロ
ピレン共及び/又は三元重合体、ポリ塩化ビニル、エチ
レンエチルアクリレート、アタクチックプロピレン及び
/又はエチレンビニルアセテートを含有する、特許請求
の範囲第1項から第7項までのいずれか1項記載の消し
ゴム。 9、ポリブタジエン、ポリアルキルベンゼン、パラフイ
ン系もしくはナフテン系油及び/又はフタレート又はそ
の他のエステルを軟化剤として含有する、特許請求の範
囲第1項から第8項までのいずれか1項記載の消しゴム
。 10、炭酸カルシウム、硫化亜鉛、酸化マグネシウム、
重晶石、軽石粉、ガラス粉及び/又はフアクチスを含有
する、特許請求の範囲第1項から第9項までのいずれか
1項記載の消しゴム。 11、無機もしくは有機顔料を染料として含有する、特
許請求の範囲第1項から第10項までのいずれか1項記
載の消しゴム。 12、合成成分 5〜50重量% 充填剤 30〜85重量% フアクチス 0〜30重量% 別の添加物 0〜30重量% 軟化剤並びに場合により安 定剤及び/又は充填剤 0〜30部 から組成された材料から成る、特許請求の範囲第1項か
ら第11項までのいずれか1項記載の消しゴム。 13、熱可塑性物質がポリオレフィン共重合体である熱
可塑性物質を有する消しゴムを製造する方法において、
オレフィン内へのゴムの包埋を重合により行ない、この
場合同時にオレフィンとゴムを夫々自体でかつ相互間で
重合させることを特徴とする、熱可塑性物質を有する消
しゴムの製法。 14、熱可塑性物質がポリオレフィン共重合体である、
熱可塑性物質を有する消しゴムを製造する方法において
、まず合成成分を熱可塑性オレフィンと包埋され完全に
架橋したゴムとの重合により製造し、これらの成分を全
組成の別の成分と、均質な全混合物が形成されるまで混
合し、かつ次いで可塑化及び成形を押出機、射出成形機
、板プレス又はその他の装置で行なうことを特徴とする
、熱可塑性物質を有する消しゴムの製法。
[Scope of Claims] 1. An eraser containing a thermoplastic material, in which the thermoplastic material is a polyolefin copolymer, in which the synthetic component is a thermoplastic polyolefin, and the polyolefin is polymerized and completely crosslinked rubber is embedded. An eraser containing a thermoplastic substance, characterized in that it contains a thermoplastic substance. 2. Ethylene in which thermoplastic olefin is polymerized in situ/
Eraser according to claim 1, which is polypropylene with propylene/diene/monoolefin (EPDM). 3. The eraser according to claim 1 or 2, wherein the rubber consists of ethylene, propylene and a small amount of unconjugated diene. 4. The eraser according to claim 3, wherein the unconjugated diene is ethylidene-norbornene. 5. The eraser according to any one of claims 1 to 4, wherein the rubber is crosslinked with a sulfur crosslinking system. 6. The eraser according to claim 5, wherein the degree of crosslinking of the rubber is greater than 7×10^-^5 mol/l. 7. The eraser according to any one of claims 1 to 6, wherein the rubber has a particle size of 0.5 to 2 μm. 8. Other additives include styrene/butadiene block copolymers, styrene/isoprene rubber, ethylene/propylene co- and/or terpolymers, polyvinyl chloride, ethylene ethyl acrylate, atactic propylene and/or ethylene vinyl acetate. The eraser according to any one of claims 1 to 7, which contains: 9. The eraser according to any one of claims 1 to 8, which contains polybutadiene, polyalkylbenzene, paraffinic or naphthenic oil, and/or phthalate or other ester as a softening agent. 10, calcium carbonate, zinc sulfide, magnesium oxide,
The eraser according to any one of claims 1 to 9, which contains barite, pumice powder, glass powder, and/or phactis. 11. The eraser according to any one of claims 1 to 10, which contains an inorganic or organic pigment as a dye. 12. Synthetic components 5-50% by weight Fillers 30-85% by weight Factis 0-30% by weight Other additives 0-30% by weight Softeners and optionally stabilizers and/or fillers 0-30 parts 12. An eraser according to any one of claims 1 to 11, which is made of a material comprising: 13. A method for producing an eraser having a thermoplastic material, wherein the thermoplastic material is a polyolefin copolymer,
1. A process for producing an eraser containing a thermoplastic material, characterized in that the embedding of rubber in the olefin is carried out by polymerization, in which case the olefin and the rubber are simultaneously polymerized, each on their own and with each other. 14. The thermoplastic material is a polyolefin copolymer,
In the process of producing erasers with thermoplastics, synthetic components are first produced by polymerization of thermoplastic olefins and embedded, fully crosslinked rubber, and these components are combined with other components of the total composition and in a homogeneous total composition. A process for producing erasers with thermoplastics, characterized in that the mixture is mixed until a mixture is formed, and then plasticization and shaping are carried out in an extruder, injection molding machine, plate press or other equipment.
JP60034716A 1984-02-25 1985-02-25 Eraser having thermoplastic material and method for producing the same Expired - Lifetime JPH0773958B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3406896.1 1984-02-25
DE3406896A DE3406896C2 (en) 1984-02-25 1984-02-25 Eraser with thermoplastic substance and process for its manufacture

Publications (2)

Publication Number Publication Date
JPS615998A true JPS615998A (en) 1986-01-11
JPH0773958B2 JPH0773958B2 (en) 1995-08-09

Family

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Application Number Title Priority Date Filing Date
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Country Link
JP (1) JPH0773958B2 (en)
DE (1) DE3406896C2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01105799A (en) * 1987-07-31 1989-04-24 Pentel Kk Eraser composition
WO2000018588A1 (en) * 1998-09-25 2000-04-06 Mitsui Chemicals, Inc. Composition for eraser rubber

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3723800A1 (en) * 1987-07-18 1989-02-02 Bayer Ag Use of EPDM materials as pencil erasers
DE3810027A1 (en) * 1988-03-24 1989-10-05 Pelikan Ag ERASER

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5213541A (en) * 1975-07-21 1977-02-01 Monsanto Co Thermoplastic elastomeric composition
JPS54124066A (en) * 1978-03-22 1979-09-26 Shinetsu Polymer Co Method of making pvc resin eraser
JPS584072A (en) * 1981-06-30 1983-01-11 松下電工株式会社 Door lock system

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4130535A (en) * 1975-07-21 1978-12-19 Monsanto Company Thermoplastic vulcanizates of olefin rubber and polyolefin resin

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5213541A (en) * 1975-07-21 1977-02-01 Monsanto Co Thermoplastic elastomeric composition
JPS54124066A (en) * 1978-03-22 1979-09-26 Shinetsu Polymer Co Method of making pvc resin eraser
JPS584072A (en) * 1981-06-30 1983-01-11 松下電工株式会社 Door lock system

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01105799A (en) * 1987-07-31 1989-04-24 Pentel Kk Eraser composition
WO2000018588A1 (en) * 1998-09-25 2000-04-06 Mitsui Chemicals, Inc. Composition for eraser rubber

Also Published As

Publication number Publication date
JPH0773958B2 (en) 1995-08-09
DE3406896A1 (en) 1985-09-05
DE3406896C2 (en) 1986-12-11

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