JPS60190440A - Filler for rubber or resin - Google Patents
Filler for rubber or resinInfo
- Publication number
- JPS60190440A JPS60190440A JP4602884A JP4602884A JPS60190440A JP S60190440 A JPS60190440 A JP S60190440A JP 4602884 A JP4602884 A JP 4602884A JP 4602884 A JP4602884 A JP 4602884A JP S60190440 A JPS60190440 A JP S60190440A
- Authority
- JP
- Japan
- Prior art keywords
- filler
- rubber
- calcium carbonate
- average particle
- resin
- 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
Links
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は充填剤、更に評しくけゴム、樹脂の充填剤に関
するものである0
ゴム材、樹脂材などを加熱溶融して特定の形に成型する
さい、得られる成形体中に気泡が生じ、該成形体の強度
を特徴とする特性を低下させる。このだめに微細な脚酸
カルシウム又はけい素鉄若しくは金属けい素を製錬する
さい発生するダス[をゴム、又は樹脂などの成型時に添
加混練してきた。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a filler, and more particularly to a filler for rubber and resin. Air bubbles form in the body, reducing the properties characterized by strength of the molded body. The dust generated during the smelting of extremely fine calcium legate, iron silicon, or silicon metal has been added and kneaded during the molding of rubber or resin.
しかし、このよう碌充填剤を用いても得られる成形体に
は気泡が多く見られ、これにともない強度が低下した。However, even when such a strong filler is used, many air bubbles are observed in the molded product obtained, and the strength is accordingly reduced.
かつ、成1形体の表面にはブルーム現象が生じ易い欠点
がおった。In addition, the surface of the molded article had a drawback that a bloom phenomenon was likely to occur.
本発明者はこのような欠点が見られないゴム又は樹脂の
充填剤をめて研究した結果微細な粒子径を有する炭酸カ
ルシウム、酸化カルシウム及びアルミナケイ酸カリウム
質粘土から混合組成物が前記充填剤としてゴム成形体又
は樹脂成形体にすぐれた性質を与えるとの知見を得て本
発明を完成するにいたった。The present inventor conducted research on rubber or resin fillers that do not have such drawbacks, and as a result, a mixed composition of calcium carbonate, calcium oxide, and potassium alumina silicate clay having fine particle sizes was found to be the filler. This led to the completion of the present invention based on the knowledge that this method imparts excellent properties to rubber molded articles or resin molded articles.
すなわち本発明の要旨は微細な粒子径を有する炭酸カル
シウム、酸化カルシウム及びアルミナケイ酸カリウム實
粘土からなる混合組成物を主成分とする充填剤である。That is, the gist of the present invention is a filler whose main component is a mixed composition of calcium carbonate, calcium oxide, and potassium alumina silicate clay having a fine particle size.
微細な粒子径を有する炭酸カルシウムは慣用の方法で炭
酸カルシウム(石灰石)を微粉砕してふるい別する方法
により得られる。また炭酸石灰を焼成して得られた酸化
カルシウムに炭酸ガスを通ずれば、平均粒子径が0.0
2μm以下のものが得られる。このものを用いた場合に
はゴム、又は樹脂の成形体は気泡が生じなくなり一段と
特性がよくなる。Calcium carbonate having a fine particle size can be obtained by pulverizing calcium carbonate (limestone) and sieving it in a conventional manner. Furthermore, if carbon dioxide gas is passed through calcium oxide obtained by calcining lime carbonate, the average particle size will be 0.0
One with a diameter of 2 μm or less can be obtained. When this material is used, the rubber or resin molded product will not have bubbles and will have even better properties.
炭酸カルシウムの粒子径が1μm以上であると充填剤が
11I&又はゴムによる1ぬれ”が生じなくなり好まし
くない。If the particle size of calcium carbonate is 1 μm or more, the filler will not be wetted by 11I & or rubber, which is not preferable.
酸化カルシウムは慣用の方法で炭酸石灰を焼成し、得ら
れた酸化カルシウムを微粉砕することにより得られる。Calcium oxide can be obtained by calcining lime carbonate in a conventional manner and pulverizing the resulting calcium oxide.
アルミナケイ酸カリウム系粘土にはセリサイ) (ga
、ox、o・3Al、0.・6H,O)が例示され、使
用にあたっては微粉砕して平均粒子径が1μm以下であ
ることが望ましい。alumina potassium silicate clay) (ga)
, ox, o.3Al, 0.・6H, O) is exemplified, and it is preferable that it is finely pulverized to have an average particle size of 1 μm or less when used.
本発明の充填剤の組成は0゜0成分が20〜90重量部
、炭酸カルシウムが10〜50重量部、アルミナケイ酸
カリウム系粘土が10〜30重量部であることが望まし
い。The composition of the filler of the present invention is preferably 20 to 90 parts by weight of the 0°0 component, 10 to 50 parts by weight of calcium carbonate, and 10 to 30 parts by weight of potassium alumina silicate clay.
本発明の充填剤を用いて、ゴム、又#′i耐iの成形体
を@造するには、ゴム又は樹脂の基材にステアリン酸、
亜鉛華、いおう、カーボン等の添加剤及び本発明の充填
剤を加えて混練成型することによって得られる。In order to produce a molded article of rubber or #'i resistance using the filler of the present invention, stearic acid is added to the rubber or resin base material.
It is obtained by adding additives such as zinc white, sulfur, and carbon and the filler of the present invention and kneading and molding.
本発明の充填剤を用いてゴム又は樹脂を混練成型すれば
、得られる成形体は気泡含有量が少なく、かつ強度が低
下することがない。If rubber or resin is kneaded and molded using the filler of the present invention, the resulting molded product will have a small bubble content and will not have a decrease in strength.
また、長時間放置してもブルーム現象がみられない。Further, no bloom phenomenon is observed even if left for a long time.
このブルーム現象が阻止されるのは理論的には不明であ
るが酸化カルシウム、炭酸カルシウム、アルミケイ酸カ
リウム系粘土の破砕面の結晶形が異なり、混合した時に
隙間なく交錯して、ゴム、1illlW成形体を充実さ
せ、ブルーム現象を生じさせる物質がゴム、又は樹脂成
形体の内部から表面に移行するのを阻止するものと思わ
れる。Although it is theoretically unclear how this blooming phenomenon is prevented, the crystal shapes of the fractured surfaces of calcium oxide, calcium carbonate, and potassium aluminosilicate clay are different, and when mixed, they intersect without any gaps, forming rubber and 1illllW molding. It is thought that it fills up the body and prevents substances that cause the bloom phenomenon from migrating from the inside of the rubber or resin molded product to the surface.
つぎに本発明を実施例について説明するが本発明はこれ
らによって限定されるものではない。Next, the present invention will be explained with reference to Examples, but the present invention is not limited thereto.
実施例1
慣用の生石灰を微粉砕して、平均粒子径を1μmとした
ものを50重量部、炭酸カルシウムを焼成して酸化カル
シウムとし、得られた酸化カルシウムを炭酸化して得ら
れた炭酸カルシウム〔平均粒子径が0.02μm〕を3
0重量部及びセリサイト粘土(微粉砕して平均1μmと
したもの〕20重量部を混合して得られた組成物をゴム
材の充填剤(6)とした。Example 1 Calcium carbonate obtained by pulverizing common quicklime to an average particle size of 1 μm, 50 parts by weight, calcining calcium carbonate to obtain calcium oxide, and carbonating the obtained calcium oxide. The average particle diameter is 0.02 μm]
A composition obtained by mixing 0 parts by weight and 20 parts by weight of sericite clay (finely pulverized to an average size of 1 μm) was used as a filler (6) for a rubber material.
この充填剤を下記に示す配合割合でそれぞれ混合し、得
られたそれぞれの混合組成物を10×10×1OcIn
の金属製の箱に入れ常圧で120℃にて加熱成型した。These fillers were mixed in the proportions shown below, and each of the resulting mixed compositions was mixed with 10 x 10 x 1 OcIn.
It was placed in a metal box and heated and molded at 120°C under normal pressure.
得られた成形体のそれぞれについて膨張率、見掛比重、
真比重をめ得た結果を第2表に示す。膨張率は下記の式
に従ってめfC。The expansion coefficient, apparent specific gravity, and
Table 2 shows the results of determining the true specific gravity. The expansion rate is fC according to the formula below.
さらに実施例1〜3及び比較例1〜3及びブランク品の
それぞれを150℃で表3に示される時間加硫し、得ら
れた加硫品について300%引張応力、伸び、引張強さ
及び硬度をJIBK6301によってめて得た結果を表
3に示す。Further, each of Examples 1 to 3, Comparative Examples 1 to 3, and the blank product was vulcanized at 150°C for the time shown in Table 3, and the resulting vulcanized products had 300% tensile stress, elongation, tensile strength, and hardness. Table 3 shows the results obtained using JIBK6301.
第 2 表
膨張率C%)
ブランク 0 27.2 0.889 1.131比較
例1 5 8.8 1.0?9 1.154比較例2
10 4.4 1.124 1.1’73比較例3 1
5 B、4 1.150 1.189実施例1 5 7
.8 1.078 1.153実施例2 10 B、7
1.141 1.183冥施例3 15 2.3 1
.167 1.194真比重ニブレスゴム板
見掛比重;オーブンゴム板
第 3 表
加硫ゴム−膜物性試験(プレス加硫)
JIB K 6301に準拠
さらにまた、ブランク、比較例1〜3及び実施例1〜3
の組成1物のそれぞれをオーブン加硫150℃で60分
間(常圧)で加硫し、得られた加硫品のそれぞれを熱空
気加硫収縮試験を行ない、得た結果を表4に示す。Table 2 Expansion rate C%) Blank 0 27.2 0.889 1.131 Comparative example 1 5 8.8 1.0?9 1.154 Comparative example 2
10 4.4 1.124 1.1'73 Comparative Example 3 1
5 B, 4 1.150 1.189 Example 1 5 7
.. 8 1.078 1.153 Example 2 10 B, 7
1.141 1.183 Meiji Example 3 15 2.3 1
.. 167 1.194 True specific gravity Apparent specific gravity of nibbles rubber plate; Oven rubber plate No. 3 Table Vulcanized rubber - Film physical property test (press vulcanization) Based on JIB K 6301 Furthermore, blank, Comparative Examples 1 to 3 and Examples 1 to 3
Each of the compositions 1 was vulcanized in an oven at 150°C for 60 minutes (normal pressure), and each of the obtained vulcanized products was subjected to a hot air vulcanization shrinkage test, and the results are shown in Table 4. .
また、それぞれについて加硫度試験を行ない得た結果を
第5表に示す。Further, a vulcanization degree test was conducted on each of the samples, and the results are shown in Table 5.
第 4 表
熱空気加硫収縮試験
オーブン加硫150℃X60分(常圧)収縮率(%〕列
理平行 直角方向
表2から明らかなように実施例品は同じ充填剤の添加し
た比較例品と対比すると膨張率が小さいことがめられた
。また、真比重も実施例品のほうが比較例品に比して大
きいことから、実施例品は比較例品に比して気泡が多く
含まれているといえる。このことは肉眼の観察の結果と
一致した。Table 4 Hot air vulcanization shrinkage test Oven vulcanization at 150°C for 60 minutes (normal pressure) Shrinkage rate (%) Parallel grain Perpendicular direction As is clear from Table 2, the example products are the comparative example products with the same filler added. It was found that the expansion rate was smaller when compared to the comparison example product.The true specific gravity of the example product was also larger than that of the comparative example product, indicating that the example product contained more air bubbles than the comparative example product. This was consistent with the results of visual observation.
また、表3から実施例品は同じ充填剤が同じで、かつ、
加硫時間が同じである比較例品と対比すると、いずれの
場合も300%引張応力、伸び及び引張強さが大である
ことがめられた。Also, from Table 3, the example products have the same filler, and
When compared with the comparative example products with the same vulcanization time, it was found that the 300% tensile stress, elongation, and tensile strength were greater in all cases.
かつ、第4表から明らかなように実施例品は比較例品に
比し、充填剤の添加量を多くしても、製品の収縮率の変
化が小δいことがめられた。Furthermore, as is clear from Table 4, it was found that the change in the shrinkage rate of the product was smaller δ in the Example product than in the Comparative Example product even when the amount of filler added was increased.
かつ、また、それぞれの製品を1か刃室内に放置して、
それぞれの製品についてプルーム現象を観察した。観察
の結果比較例品及びブランク品にはブルーム現象が認め
られたが、実施例品にはほとんど認められなかった。Also, leave one of each product in the blade chamber,
Plume phenomena were observed for each product. As a result of observation, a bloom phenomenon was observed in the comparative example product and the blank product, but almost no bloom phenomenon was observed in the example product.
実施例4〜6
実施例1に用いた炭酸カルシウム(平均粒子径が0.0
2μm)の代りに平均粒子径が1μmを用いた以外は実
施例1に準じて充填剤を調製第 5 表 1膨張率(%
)
実施例4 5 8.Ol、075 1.153実施例5
to 4.0 1.133 1.184実施例6 1
5 2.9 1.159 1.193第6表
加硫ゴム−膜物性試験(プレス加硫)
JI8 K 6301に準拠
第 7 表
熱空気加硫収縮試験
オープン加硫150℃X60分(常FE)収縮率(%)
列理平行 直角方向
この充填剤と、実施例1に用いた基材ム及び添加剤Bと
を実施例1に準じて混合し成型し、得られた成形体を実
施例1に準じて物性を測宇した。また、その成形体を実
施例1に準じて加硫化し、得られた製品についての諸物
件を測宇した。得られた結果を第5−7表に示す。Examples 4 to 6 Calcium carbonate used in Example 1 (average particle size 0.0
A filler was prepared according to Example 1, except that particles with an average particle size of 1 μm were used instead of 2 μm.
) Example 4 5 8. Ol, 075 1.153 Example 5
to 4.0 1.133 1.184 Example 6 1
5 2.9 1.159 1.193 Table 6 Vulcanized rubber - Membrane physical property test (press vulcanization) Based on JI8 K 6301 Table 7 Hot air vulcanization shrinkage test Open vulcanization 150°C x 60 minutes (normal FE) Shrinkage factor(%)
Parallel grain, perpendicular direction This filler, the base material and additive B used in Example 1 were mixed and molded according to Example 1, and the physical properties of the obtained molded body were evaluated according to Example 1. I measured it. Further, the molded body was vulcanized according to Example 1, and various properties of the obtained product were measured. The results obtained are shown in Table 5-7.
これらの結果から、実施例品4〜6のそれぞれは充填剤
の種類を異にするが、含有率が同じである比較例品1〜
3のそれぞれと対応してみると、実施例品はこれと対応
する比較例品よりすぐれているが、実施例品1〜3に比
し若干低下するのが見られた。From these results, it can be seen that Example products 4 to 6 have different filler types, but Comparative Example products 1 to 6 have the same content.
3, the example product was superior to the corresponding comparative example product, but was seen to be slightly lower than the example products 1 to 3.
特許出願人 株式会社サンケイカル 代理人弁理士 漫 野 豐 司Patent applicant: Sankeikaru Co., Ltd. Representative Patent Attorney Tsukasa Manno
Claims (1)
炭酸カルシウム及びアルミナケイ酸カリウム系粘土を含
むことをellとするゴム、又はW脂の充填剤 (2、特許請求の範囲第1項において炭酸カルシウムが
、炭醗石灰を焼成して酸化カルシウムとし、ついでこれ
に炭酸ガスを通じて炭酸カルシウムとし、平均粒子を0
.02μm以下としたものであるゴム又はti1脂の充
填剤(3)特許請求の範囲第1項又は第2項において酸
化カルシウムが20〜90重量部、炭酸カルシウムが1
0〜50重量部及びアルミナケイ酸系粘土が10〜30
重量部であることを特徴とするゴム又は樹脂の充填剤 (4)特許請求の範囲第1項から第3項のいずれかにお
いてアルミナケイ酸カリウム粘土がセリサイトであるゴ
ム又はm詣の充填剤[Scope of Claims] (1) Calcium oxide having an average particle diameter of 1 μm or less;
Rubber or W fat filler containing calcium carbonate and potassium alumina silicate clay (2. In claim 1, calcium carbonate is made by calcining carbonated lime to form calcium oxide, Next, carbon dioxide gas is passed through this to make calcium carbonate, and the average particle size is reduced to 0.
.. Rubber or Ti1 fat filler having a particle size of 0.02 μm or less
0 to 50 parts by weight and 10 to 30 parts by weight of alumina-silicate clay
(4) Rubber or resin filler characterized in that the amount is parts by weight (4) A filler for rubber or resin according to any one of claims 1 to 3, in which the potassium alumina silicate clay is sericite.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4602884A JPS60190440A (en) | 1984-03-10 | 1984-03-10 | Filler for rubber or resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4602884A JPS60190440A (en) | 1984-03-10 | 1984-03-10 | Filler for rubber or resin |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60190440A true JPS60190440A (en) | 1985-09-27 |
JPH0522731B2 JPH0522731B2 (en) | 1993-03-30 |
Family
ID=12735586
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4602884A Granted JPS60190440A (en) | 1984-03-10 | 1984-03-10 | Filler for rubber or resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60190440A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111909424A (en) * | 2020-07-07 | 2020-11-10 | 广西夏阳环保科技有限公司 | Preparation method and application of modified nano calcium carbonate for rubber |
-
1984
- 1984-03-10 JP JP4602884A patent/JPS60190440A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111909424A (en) * | 2020-07-07 | 2020-11-10 | 广西夏阳环保科技有限公司 | Preparation method and application of modified nano calcium carbonate for rubber |
CN111909424B (en) * | 2020-07-07 | 2022-06-17 | 都安春旭新材料科技有限责任公司 | Preparation method and application of modified nano calcium carbonate for rubber |
Also Published As
Publication number | Publication date |
---|---|
JPH0522731B2 (en) | 1993-03-30 |
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