JPH0413769A - Flowability improver and its composition - Google Patents
Flowability improver and its compositionInfo
- Publication number
- JPH0413769A JPH0413769A JP11517590A JP11517590A JPH0413769A JP H0413769 A JPH0413769 A JP H0413769A JP 11517590 A JP11517590 A JP 11517590A JP 11517590 A JP11517590 A JP 11517590A JP H0413769 A JPH0413769 A JP H0413769A
- Authority
- JP
- Japan
- Prior art keywords
- fluidity
- resin
- compound
- impact strength
- composition
- 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
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、環状ポリジアルキルシロキサン化合物を主成
分とし、熱可塑性樹脂に好適に使用し得る流動性改良剤
に関する。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a fluidity improver that contains a cyclic polydialkylsiloxane compound as a main component and can be suitably used for thermoplastic resins.
〔従来の技術及び発明が解決しようとする課題〕ポリプ
ロピレン(以下、PPと略す)は汎用樹脂として多用さ
れており、JIS−に6747に示されるように重合形
式やメルトフローレート(以下、MFRと略す)により
数々の種類に分類されている。上記VFRはその樹脂の
成型性を判断する上で、重要な項目であり、MFRが大
きいほど溶融粘度が低く、成型しやすい樹脂と言える。[Prior art and problems to be solved by the invention] Polypropylene (hereinafter abbreviated as PP) is widely used as a general-purpose resin, and as shown in JIS-6747, polymerization type and melt flow rate (hereinafter referred to as MFR) are widely used. (abbreviated)) are classified into many types. The above-mentioned VFR is an important item in determining the moldability of the resin, and the larger the MFR, the lower the melt viscosity, and it can be said that the resin is easier to mold.
一方、PPの物性の中で特に重要な物性である衝撃強度
は、PPのMFRが小さいほど大きくなる。このため、
衝撃強度が要求される用途には、MFRが小さく成型し
にくい樹脂を使用しなければならず、成型性が悪いとい
う問題が生じている。On the other hand, impact strength, which is a particularly important physical property among the physical properties of PP, increases as the MFR of PP decreases. For this reason,
For applications that require impact strength, resins that have a small MFR and are difficult to mold must be used, resulting in the problem of poor moldability.
そこで、衝撃強度と成型性が共に優れたPPを得るため
に、MFRの小さいPPの流動性を改良する試みがなさ
れている。PPの流動性を改良する方法として、「ボリ
マーダ・インエストJ 1988年11月号106真に
ポリジメチルシロキサンを添加する方法が記載されてい
る。そこで、本発明者らが、PP100重量部にポリジ
メチルシロキサン3重量部を添加したところ、ポリジメ
チルシロキサン無添加のPPに比べてMFRは3,5倍
に向上し、衝撃強度の低下は見られなかったが、ポリジ
メチルシロキサンがPPに相溶しないためにPPの白化
及びポリジメチルシロキサンのブリードアウトによる装
置の汚染、PPの流れむら及びPPの表面特性の変化等
の問題が生した。Therefore, attempts have been made to improve the fluidity of PP with a small MFR in order to obtain PP with excellent impact strength and moldability. As a method for improving the fluidity of PP, a method of adding polydimethylsiloxane to 100 parts by weight of PP is described in "Bolimada Inest J, November 1988 Issue 106." When 3 parts by weight of siloxane was added, MFR improved 3.5 times compared to PP without polydimethylsiloxane, and no decrease in impact strength was observed, but this is because polydimethylsiloxane is not compatible with PP. Problems such as contamination of equipment due to whitening of PP and bleed-out of polydimethylsiloxane, uneven flow of PP, and changes in surface properties of PP occurred.
本発明者らは上記の課題を解決すべく各種のシロキサン
化合物を合成してPPさらには熱可塑性樹脂全般への添
加効果を検討してきた。その結果、特定の環状ポリジア
ルキルシロキサンが少量の添加で、樹脂の衝撃強度を低
下させることなく該化合物のブリードアウトによる問題
をおこさず、流動性を著しく向上させることを見いだし
、本発明を提供するに至った。In order to solve the above problems, the present inventors have synthesized various siloxane compounds and have studied the effects of adding them to PP and thermoplastic resins in general. As a result, it was discovered that when a small amount of a specific cyclic polydialkylsiloxane is added, the fluidity is significantly improved without reducing the impact strength of the resin, without causing problems due to bleed-out of the compound, and providing the present invention. reached.
即ち、本発明は、下記一般式(1)
で示される環状ポリジアルキルシロキサン化合物よりな
る流動性改良剤である。That is, the present invention is a fluidity improver comprising a cyclic polydialkylsiloxane compound represented by the following general formula (1).
上記一般式(1)中、R1及びR2は、炭素原子数が3
〜16のアルキル基である。炭素原子数が2以下の場合
はブリードアウトが発生する。また、炭素原子数が17
以上の場合は、本発明の環状ポリジアルキルシロキサン
化合物を熱可塑性樹脂に添加しても流動性の改良が不十
分であり、熱可塑性樹脂の改質を十分に行うことができ
ない。In the above general formula (1), R1 and R2 have 3 carbon atoms.
~16 alkyl groups. If the number of carbon atoms is 2 or less, bleed-out occurs. Also, the number of carbon atoms is 17
In the above cases, even if the cyclic polydialkylsiloxane compound of the present invention is added to the thermoplastic resin, the fluidity is not sufficiently improved, and the thermoplastic resin cannot be sufficiently modified.
R1及びR2で示されるアルキル基の炭素原子数は上記
の範囲であればよいが、特に3〜12の範囲であること
が好ましい。R1及びR2で示されるアルキル基は、直
鎖及び分岐の区別なく用いることができる。The number of carbon atoms in the alkyl group represented by R1 and R2 may be within the above range, but is particularly preferably within the range of 3 to 12. The alkyl groups represented by R1 and R2 can be used regardless of whether they are linear or branched.
上記一般式(1)中、nは3又は4である。nが3又は
4以外の値の化合物は不安定であるために好ましくない
。In the general formula (1) above, n is 3 or 4. Compounds in which n is other than 3 or 4 are unstable and are therefore not preferred.
上記一般式[)で示される環状ポリジアルキルシロキサ
ン化合物は、公知の方法により容易に製造することがで
きる。The cyclic polydialkylsiloxane compound represented by the above general formula [) can be easily produced by a known method.
一般式(1)で示される化合物は、熱可塑性樹脂に少量
添加することにより、該樹脂の衝撃強度を低下させずに
、該樹脂からのブリードアウトによる問題を発生させる
ことな(、該樹脂の流動性を著しく向上させることがで
きる。熱可塑性樹脂は、公知のものが何ら制限なく用い
ることができ、例えば、ポリオレフィン、ポリ塩化ビニ
ル、ポリスチレン、ポリアミド、ポリエステル、ポリエ
ーテル、ポリカーボネート等の各樹脂を挙げることがで
きる。就中、ポリオレフィンへの添加効果が良好である
。本発明の環状ポリジアルキルシロキサン化合物の配合
量は熱可塑性樹脂100重量部に対して、0.1〜20
重量部の範囲であり、より好ましくは0.5〜10重量
部である。配合量が0.1重量部未満の場合は流動性を
向上させる効果が乏しく、また、配合量が20重量部を
越えると熱可塑性樹脂の物性を低下させる場合があり、
好ましくない。By adding a small amount of the compound represented by the general formula (1) to a thermoplastic resin, it can be used without reducing the impact strength of the resin and without causing problems due to bleed-out from the resin. Fluidity can be significantly improved.As the thermoplastic resin, any known thermoplastic resin can be used without any restriction.For example, various resins such as polyolefin, polyvinyl chloride, polystyrene, polyamide, polyester, polyether, and polycarbonate can be used. In particular, the effect of addition to polyolefins is good.The amount of the cyclic polydialkylsiloxane compound of the present invention is 0.1 to 20 parts by weight per 100 parts by weight of the thermoplastic resin.
The amount ranges from 0.5 to 10 parts by weight, more preferably from 0.5 to 10 parts by weight. If the amount is less than 0.1 parts by weight, the effect of improving fluidity will be poor, and if the amount exceeds 20 parts by weight, the physical properties of the thermoplastic resin may be deteriorated.
Undesirable.
本発明の一般式〔1)で示される環状ポリジアルキルシ
ロキサン化合物は、熱可塑性樹脂の衝撃強度を低下させ
ることなく、熱可塑性樹脂から該化合物のブリードアウ
トによる問題が発生せず、熱可塑性樹脂の流動性を著し
く向上させる。具体的に述べると、例えばPP100重
量部に対して、一般式CI)で示される化合物のうちR
1及びR2が共にオクチル基である化合物を3重量部添
加すると、PPの流動性は一般式CI)で示される化合
物を添加していないPPの流動性に比べて3倍に向上し
、PPの衝撃強度の低下は見られなかった。また、PP
の白化及び該環状ポリジオクチルシロキサンのPPから
のブリードアウトという問題も発生しなかった。一方、
ポリジメチルシロキサンを上記と同量添加した場合、P
Pの流動性は無添加に比べて3.5倍に向上し、PPの
衝撃強度の低下は見られなかったが、PPの白化及び該
ポリジメチルシロキサンのPPからのブリードアウトが
生じた。この特異な効果は後述する実施例及び比較例の
対比で明らかなように、一般式CI)で示される化合物
のアルキル基の炭素原子数が3〜16の場合にのみ発現
される効果である。The cyclic polydialkylsiloxane compound represented by the general formula [1) of the present invention does not reduce the impact strength of the thermoplastic resin, does not cause problems due to bleed-out of the compound from the thermoplastic resin, and is suitable for use in thermoplastic resins. Significantly improves fluidity. Specifically, for example, R of the compound represented by the general formula CI) with respect to 100 parts by weight of PP
When 3 parts by weight of a compound in which 1 and R2 are both octyl groups is added, the fluidity of PP is improved three times compared to that of PP without the compound represented by the general formula CI). No decrease in impact strength was observed. Also, PP
Problems such as whitening of the PP and bleed-out of the cyclic polydioctylsiloxane from the PP did not occur. on the other hand,
When adding the same amount of polydimethylsiloxane as above, P
The fluidity of P was improved by 3.5 times compared to the case without addition, and no decrease in the impact strength of PP was observed, but whitening of PP and bleed-out of the polydimethylsiloxane from PP occurred. As will be clear from the comparison of Examples and Comparative Examples described later, this unique effect is an effect that is expressed only when the alkyl group of the compound represented by the general formula CI) has 3 to 16 carbon atoms.
(実施例)
本発明を更に具体的に説明するため、以下実施例および
比較例をあげて説明するが、本発明はこれらの実施例に
なんら限定されるものではない。(Examples) In order to explain the present invention more specifically, Examples and Comparative Examples will be described below, but the present invention is not limited to these Examples at all.
なお、実施例および比較例中に示した樹脂の流動性はJ
IS K7210によって測定し、衝撃強度はJISK
7110によって測定した。また、添加物のブリードア
ウト試験は樹脂を成型後、温度23±2℃、相対湿度5
0±5%の状態で1週間保存したサンプルをn−ヘキサ
ンに10分間浸漬し、溶出した添加物の量を浸漬試験前
のサンプル中に含まれていた添加物の量で除して百分率
で表した。In addition, the fluidity of the resin shown in the examples and comparative examples is J
Measured by IS K7210, impact strength is JISK
7110. In addition, additive bleed-out tests were carried out after molding the resin at a temperature of 23 ± 2°C and a relative humidity of 5.
A sample stored for one week at 0 ± 5% is immersed in n-hexane for 10 minutes, and the amount of eluted additive is divided by the amount of additive contained in the sample before the immersion test to calculate the percentage. expressed.
実施例1
ヘキサオクチルシクロトリシロキサン(以下、0ctD
zと略す)3gとPP(徳山曹達株式会社製RB−41
0) 100gをロール機を用い、180℃で5分間混
練した。その後このPPのMFRを測定したところ、0
ctlh無添加のPPに比べて3倍に向上した。Example 1 Hexaoctylcyclotrisiloxane (hereinafter referred to as 0ctD
abbreviated as z) 3g and PP (RB-41 manufactured by Tokuyama Soda Co., Ltd.)
0) 100g was kneaded at 180°C for 5 minutes using a roll machine. After that, we measured the MFR of this PP and found that it was 0.
It was improved three times compared to PP without ctlh addition.
このPPをJIS K6758に従って成型した。成形
されたPPの衝撃強度は0ctD、無添加のPPに比べ
て変化しなかった。PPの外観は0ctDz無添加のP
Pと同じであり、PPの白化は観察されなかった。また
、Oc tD、のブリードアウト試験をしたところ0c
tD、は検出されなかった。This PP was molded according to JIS K6758. The impact strength of the molded PP was 0 ctD, which did not change compared to PP without additives. The appearance of PP is 0ctDz-free P.
P, and no whitening of PP was observed. Also, when I did a bleed-out test for OctD, it was 0c.
tD was not detected.
実施例2
実施例1において、PPを表−1に示す樹脂に変更した
以外はすべて実施例1と同様に行った。Example 2 Everything was carried out in the same manner as in Example 1 except that PP was changed to the resin shown in Table 1.
結果を表−1に示した。The results are shown in Table-1.
実施例3
実施例1において、0ctD3の代りに表−2に示ス環
状ポリジアルキルシロキサンを表−2に示す量用いた他
は実施例1と同様な操作を行い、PPの物性を測定した
。結果を表−2に示した。Example 3 The same procedure as in Example 1 was performed except that cyclic polydialkylsiloxane shown in Table 2 was used in the amount shown in Table 2 instead of 0ctD3, and the physical properties of PP were measured. The results are shown in Table-2.
比較例1
実施例1において0ctD、の代りに表−3に示す化合
物を使用した他は実施例1と同様な操作を行い、PPの
物性を測定した。結果を表−3に示した。Comparative Example 1 The same operations as in Example 1 were performed except that the compounds shown in Table 3 were used instead of 0ctD in Example 1, and the physical properties of PP were measured. The results are shown in Table-3.
Claims (2)
子数3〜16のアルキル基であり、nは3又は4である
。 で示される環状ポリジアルキルシロキサン化合物よりな
る流動性改良剤。(1) General formula ▲ There are mathematical formulas, chemical formulas, tables, etc. ▼ However, R^1 and R^2 are the same or different alkyl groups having 3 to 16 carbon atoms, respectively, and n is 3 or 4. . A fluidity improver comprising a cyclic polydialkylsiloxane compound represented by:
シロキサン化合物0.1〜20重量部 よりなる組成物。(2) A composition comprising (a) 100 parts by weight of a thermoplastic resin and (b) 0.1 to 20 parts by weight of the cyclic polydialsiloxane compound described in claim (1).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11517590A JPH0819335B2 (en) | 1990-05-02 | 1990-05-02 | Fluidity improver and composition thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11517590A JPH0819335B2 (en) | 1990-05-02 | 1990-05-02 | Fluidity improver and composition thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0413769A true JPH0413769A (en) | 1992-01-17 |
| JPH0819335B2 JPH0819335B2 (en) | 1996-02-28 |
Family
ID=14656203
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11517590A Expired - Lifetime JPH0819335B2 (en) | 1990-05-02 | 1990-05-02 | Fluidity improver and composition thereof |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0819335B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0596730A1 (en) * | 1992-11-06 | 1994-05-11 | Shin-Etsu Chemical Co., Ltd. | Cyclotrisiloxane and process for producing the same |
| US12043638B2 (en) * | 2017-09-22 | 2024-07-23 | 3M Innovative Properties Company | Cyclic siloxanes, compositions, methods, and articles |
-
1990
- 1990-05-02 JP JP11517590A patent/JPH0819335B2/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0596730A1 (en) * | 1992-11-06 | 1994-05-11 | Shin-Etsu Chemical Co., Ltd. | Cyclotrisiloxane and process for producing the same |
| US12043638B2 (en) * | 2017-09-22 | 2024-07-23 | 3M Innovative Properties Company | Cyclic siloxanes, compositions, methods, and articles |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0819335B2 (en) | 1996-02-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2803300B2 (en) | Stabilized polypropylene resin composition | |
| CA1138147A (en) | Thermoplastic blend of polypropylene, epm and propylene-ethylene copolymer | |
| CA2174053A1 (en) | Polypropylene molding composition containing an antistatic agent and having low-fogging properties | |
| JPH0413769A (en) | Flowability improver and its composition | |
| JPS60124642A (en) | Stabilized polyolefin composition | |
| JPS62115049A (en) | Impact-resistant polypropylene composition | |
| EP0426315A2 (en) | Polypropylene resin composition | |
| JPS6254819B2 (en) | ||
| JPS58210950A (en) | Propylene polymer resin composition | |
| JPS59210962A (en) | Polypropylene resin composition | |
| JPS62241942A (en) | Propylene polymer composition | |
| JPH07138434A (en) | Styrene resin composition | |
| JP4493740B2 (en) | Polyoxymethylene resin coloring composition and molded article | |
| JPH0436341A (en) | Polyacetal resin composition | |
| JP2541708B2 (en) | Flame retardant polypropylene composition | |
| JPH06200171A (en) | Resin composition having excellent antistaticity | |
| JPH0465100B2 (en) | ||
| JP3028700B2 (en) | Polyethylene polymer alloy | |
| JPH1112409A (en) | Propylene resin composition excellent in transparency, heat resistance and impact resistance, and container | |
| JPS63130648A (en) | Polyolefin composition | |
| JPH0625541A (en) | Antistatic resin composition | |
| JPH02166141A (en) | polypropylene composition | |
| JPH0428741A (en) | Propylene resin composition | |
| JP2000178404A (en) | Propylene resin composition and its use | |
| JP3213466B2 (en) | Refrigerator interior parts |