JP2001059026A - Master batch composition - Google Patents

Master batch composition

Info

Publication number
JP2001059026A
JP2001059026A JP11272874A JP27287499A JP2001059026A JP 2001059026 A JP2001059026 A JP 2001059026A JP 11272874 A JP11272874 A JP 11272874A JP 27287499 A JP27287499 A JP 27287499A JP 2001059026 A JP2001059026 A JP 2001059026A
Authority
JP
Japan
Prior art keywords
synthetic resin
weight
parts
master batch
raw material
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.)
Pending
Application number
JP11272874A
Other languages
Japanese (ja)
Inventor
Koji Tani
宏治 谷
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to JP11272874A priority Critical patent/JP2001059026A/en
Publication of JP2001059026A publication Critical patent/JP2001059026A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain the subject composition for a synthetic resin, having excellent dispersibility not only in an ordinary molding method for synthetic resin but also in a high-speed molding method and a high concentration of master batch raw material by compounding a specific ester-based compound and the master batch raw material in a specific ratio to the synthetic resin. SOLUTION: This composition comprises (B) 5-300 pts.wt. of an ester-based compound (e.g. dibutyl cellosolve phthalate, etc.), containing at least one ether bond of the formula (X is a 2-12C alkyl, aromatic group or alicyclic dibasic acid residue; R is a 1-15C alkyl; E is a 2-4C alkylene; m is 1-7; n is 0-7) containing 0.1-5.0 wt.% of a perchlorate such as lithium perchlorate, etc., and (C) preferably >=10 pts.wt. of a master batch raw material such as dye, etc., based on (A) preferably 100 pts.wt. of a synthetic resin being a thermoplastic polyolefin-based resin. The composition is useful for coloring a synthetic resin in molding and processing.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する利用分野】合成樹脂の成形加工時に、着
色、樹脂の改質等のために添加されるマスターバッチ組
成物に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a masterbatch composition which is added during molding of a synthetic resin for coloring, modifying the resin, and the like.

【0002】[0002]

【従来の技術】現状、例えばポリオレフィン系樹脂を着
色するための染顔料の添加方法としては成形加工時にお
けるマスターバッチペレットの添加法が一般的である。
そのマスターバッチペレットの組成は、主にベース樹脂
と染顔料及び分散剤(ワックス+金属石鹸)より成り、
これらを混合、混錬、ペレット化したものであるしかし
この方法では固体の染顔料を均一に分散するためにはマ
スターバッチにおける染顔料濃度に限界がある 即ち低
濃度のマスターバッチペレットをかなりの量使用せざる
をえない状況である。又各種充填剤、添加剤を多量に添
加したい場合、低濃度のマスターバッチを大量に添加し
なければならず、経済性に問題がある更に最近の高速成
形法の普及により分散性良好なる高濃度マスターバッチ
ペレットの要求が高まっている。
2. Description of the Related Art At present, for example, as a method of adding a dye or pigment for coloring a polyolefin resin, a method of adding a master batch pellet during molding is generally used.
The composition of the masterbatch pellet is mainly composed of base resin, dye and pigment and dispersant (wax + metal soap).
These are mixed, kneaded, and pelletized.However, in this method, the concentration of the dye and pigment in the master batch is limited in order to uniformly disperse the solid dye and pigment. It is a situation that must be used. In addition, when it is desired to add a large amount of various fillers and additives, a large amount of a low-concentration masterbatch must be added, and there is a problem with economic efficiency. The demand for masterbatch pellets is increasing.

【0003】[0003]

【発明が解決しようとしている課題】合成樹脂の通常成
型法では勿論、高速成型法においても分散性良好なる高
濃度マスターバッチ組成物を提供すること
SUMMARY OF THE INVENTION It is an object of the present invention to provide a high-concentration masterbatch composition having good dispersibility not only in a general molding method of synthetic resin but also in a high-speed molding method.

【0004】[0004]

【課題を解決するための手段】本発明者は上記課題を解
決するために種々検討の結果合成樹脂用マスターバッチ
組成物としてベース合成樹脂100重量部に対し過塩素
酸塩0.1〜5.0重量%を含む次式で表される化合物
Means for Solving the Problems The present inventor has made various studies to solve the above-mentioned problems, and as a result, as a masterbatch composition for synthetic resins, perchlorate 0.1 to 5. A compound represented by the following formula containing 0% by weight

【化1】Embedded image

【0005】 (式中、Xは炭素数2〜12のアルキル基、芳香族基若
しくは脂環式の二塩基酸残基を、Rは同一又は異なって
もよい炭素数1〜15のアルキル基を、Eは炭素数2〜
4のアルキレン基を其々表し、mは1〜7の整数であ
り、nは0〜7の整数である)5〜300重量部にマス
ターバッチ原料を加えたものがマスターバッチ原料をか
なり高濃度にしても極めて分散性が良いことを見出し本
発明に至った。
[0005] (Wherein X represents an alkyl group having 2 to 12 carbon atoms, an aromatic group or an alicyclic dibasic acid residue, R represents an alkyl group having 1 to 15 carbon atoms which may be the same or different, and E represents 2 carbon atoms
4 represents an alkylene group, m represents an integer of 1 to 7, and n represents an integer of 0 to 7) A master batch material having a considerably high concentration is obtained by adding a master batch material to 5 to 300 parts by weight. Nevertheless, they found that the dispersibility was extremely good, and reached the present invention.

【0006】ここで用いられる合成樹脂としては、特に
制限はないが、添加剤に対する相溶性の小さいとされる
ポリオレフィン系樹脂が好適である。
The synthetic resin used here is not particularly limited, but a polyolefin resin which is considered to have low compatibility with additives is preferred.

【0007】(I)式で示される化合物としては、モノ
又はジブチルセロソルブフタレート、モノ又はジブチル
セロソルブアジペート、モノ又はジエチルセロソルブフ
タレート、モノ又はジエチルセロソルブアジベート等が
挙げられる。又次に示す化合物とアジピン酸とのモノ又
はジエステル、又はフタール酸とのモノ又はジエステル
を挙げることが出来る。勿論モノとジエステルとの混合
物も含まれる。エチレングリコールモノオクチルエーテ
ル、ジエチレングリコールモノメチルエーテル、ジエチ
レングリコールもノブチルエーテル、ジエチレングリコ
ールモノヘブチルエーテルトリエチレングリコールモノ
イメチルエーテル、トリエチレングリコールモノプロピ
ルエーテル、テトラエチレングリコールモノエチルエー
テル、プロピレングリコールモノエチルエーテル、プロ
ピレングリコールモノオクチルエーテル、ジプロピレン
グリコールモノブチルエーテル、ブチレングリコールモ
ノブチルエーテル添加量としては5〜300重量部で、
5重量部以下であるとその効果が小さく、300重量部
以上であると、マスターバッチを添加した成形品の表面
に滲み出し現象を起こし好ましくない
The compound represented by formula (I) includes mono- or dibutyl cellosolve phthalate, mono- or dibutyl cellosolve adipate, mono- or diethyl cellosolve phthalate, mono- or diethyl cellosolve adipate, and the like. In addition, mono- or diesters of the following compounds with adipic acid or mono- or diesters with phthalic acid can be mentioned. Of course, mixtures of mono- and diesters are also included. Ethylene glycol monooctyl ether, diethylene glycol monomethyl ether, diethylene glycol also nobutyl ether, diethylene glycol monohexyl ether triethylene glycol monomethyl ether, triethylene glycol monopropyl ether, tetraethylene glycol monoethyl ether, propylene glycol monoethyl ether, propylene glycol monooctyl Ether, dipropylene glycol monobutyl ether, butylene glycol monobutyl ether as the addition amount 5 to 300 parts by weight,
If the amount is less than 5 parts by weight, the effect is small, and if it is more than 300 parts by weight, a bleeding phenomenon occurs on the surface of the molded article to which the master batch is added, which is not preferable.

【0008】ここで用いられる過塩素酸塩としては、過
塩素酸リチウム、過塩素酸ナトリウム、過塩素酸カリウ
ム、過塩素酸バリウム、過塩素酸テトラエチルアンモニ
ウム、過塩素酸テトラプロピルアンモニウム、過塩素酸
テトラブチルアンモニウム等を挙げることが出来る添加
量は0.1〜5.0重量%の範囲であり、0.1重量%
以下だとその効果が小さく5.0重量%以上になるとベ
ースレジンの熱安定性を損ない変色する。
The perchlorate used here includes lithium perchlorate, sodium perchlorate, potassium perchlorate, barium perchlorate, tetraethylammonium perchlorate, tetrapropylammonium perchlorate, perchloric acid The amount of addition such as tetrabutylammonium is in the range of 0.1 to 5.0% by weight, and 0.1% by weight.
When the content is less than 5.0% by weight or more, the thermal stability of the base resin is impaired and discoloration occurs.

【実施例】【Example】

【0009】[0009]

【実施例1〜4、比較例1】メルトフローレート1.5
のホモ・ポリプロピレン樹脂(PJS;三井化学(株)
製)100重量部、フタロシアニンブルー(リオノーブ
ル7110V;東洋インキ製造(株)製)50重量部に
対して、過塩素酸リチウム1.5重量%含有するジブチ
ルセロソルブフタレートを各々3、10、30、10
0、200配合し、ミキサーで混合後、180℃にセッ
トした8インチ2本ロールに投入、5分間混練した約
0.4mm厚で取出したシートを冷却後、シートカッタ
ー(朋来(株)製)にて6mm角にカットしペレットと
した。このペレットを上記ホモ・ポリプロピレン樹脂1
00重量部に5重量部混合し、再び8インチ2本ロール
で3分間混練して顔料の分散性を評価した。結果を表1
に示す。
Examples 1-4, Comparative Example 1 Melt flow rate 1.5
Homopolypropylene resin (PJS; Mitsui Chemicals, Inc.)
100 parts by weight) and 50 parts by weight of phthalocyanine blue (Rio Noble 7110V; manufactured by Toyo Ink Mfg. Co., Ltd.), 3,10,30, and dibutyl cellosolve phthalate containing 1.5% by weight of lithium perchlorate, respectively. 10
After mixing with a mixer of 0 and 200, the mixture was mixed with a mixer, put into an 8-inch two-roll set at 180 ° C., kneaded for 5 minutes, and the sheet taken out with a thickness of about 0.4 mm was cooled and then cooled with a sheet cutter (manufactured by Torai Co., Ltd.) And cut into 6 mm squares to make pellets. This pellet is mixed with the homo-polypropylene resin 1
5 parts by weight were mixed with 00 parts by weight, and kneaded again with an 8-inch two-roll mill for 3 minutes to evaluate the dispersibility of the pigment. Table 1 shows the results
Shown in

【0010】[0010]

【比較例2、3】実施例のジブチルセロソルブフタレー
トの代わりにプロピレンワックス(ビスコール660
P;三洋化成(株)製)15重量部、又はポリエチレン
ワックス(サンワックス131P;三洋化成(株)製)
15重量部を配合し、実施例と同様の評価を行った 結
果を表1に示す
Comparative Examples 2 and 3 Propylene wax (Viscol 660) was used in place of dibutyl cellosolve phthalate in the examples.
P; 15 parts by weight of Sanyo Chemical Co., Ltd.) or polyethylene wax (Sunwax 131P; Sanyo Chemical Co., Ltd.)
Table 1 shows the results obtained by blending 15 parts by weight and performing the same evaluation as in the examples.

【0011】[0011]

【実施例5〜7】ポリエチレン樹脂(ハイゼックス21
00J;三井化学(株)製)100重量部、過塩素酸リ
チウム1.5重量%含有するジブチルセロソルブフタレ
ート30、50,100重量部に対し、酸化チタン(タ
イペークCR80;石原産業(株)製)を各々50,1
00,200重量部配合し、実施例1〜4と同様の評価
を行った、結果を表2に示す
Examples 5 to 7 Polyethylene resin (HIZEX 21)
00J; 100 parts by weight of Mitsui Chemicals, Inc., and 30, 50, 100 parts by weight of dibutyl cellosolve phthalate containing 1.5% by weight of lithium perchlorate, titanium oxide (Taipec CR80; manufactured by Ishihara Sangyo Co., Ltd.) To 50, 1 each
The same evaluations as in Examples 1 to 4 were carried out by mixing 00 and 200 parts by weight, and the results are shown in Table 2.

【0012】[0012]

【比較例4,5】実施例5〜7におけるジブチルセロソ
ルブフタレートの代わりにポリエチレンワックス(サン
ワックス131P;三洋化成(株)製)各々30,50
重量部を配合し同様の評価を行った。結果を表2に示す
Comparative Examples 4 and 5 Instead of dibutyl cellosolve phthalate in Examples 5 to 7, polyethylene wax (Sunwax 131P; manufactured by Sanyo Chemical Co., Ltd.) was 30, 50 respectively.
The same evaluation was performed by blending parts by weight. The results are shown in Table 2.

【0013】[0013]

【実施例8〜10、比較例6,7】ポリエチレン樹脂
(ハイゼックス2100J;三井化学(株)製)100
重量部、酸化チタン(タイペークCR80;石原産業
(株)製)200重量部、ジエチルセロソルブアジペー
ト100重量部に対し過塩素酸リチウムを各々0,0.
3,1.0,5.0,10.0重量部配合し実施例1と
同様の評価及びシートを25℃24時間放置後、シート
表面の液状物滲み出し有無の評価を行った。
Examples 8 to 10 and Comparative Examples 6 and 7 Polyethylene resin (HIZEX 2100J; manufactured by Mitsui Chemicals, Inc.) 100
Parts by weight, 200 parts by weight of titanium oxide (Taipec CR80; manufactured by Ishihara Sangyo Co., Ltd.), and 100 parts by weight of diethylcellosolve adipate, each containing lithium perchlorate in an amount of 0.0.
3, 1.0, 5.0 and 10.0 parts by weight were blended, and the same evaluation as in Example 1 was carried out, and the sheet was allowed to stand at 25 ° C. for 24 hours.

【0014】[0014]

【表1】 [Table 1]

【0015】[0015]

【表2】 [Table 2]

【0016】[0016]

【表3】 [Table 3]

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】合成樹脂100重量部に対して過塩素酸塩
0.1〜5.0重量%を含む一般化学式が次式で表され
る少なくとも一つのエーテル結合を持ったエステル系化
合物 (式中、Xは炭素数2〜12のアルキル基、芳香族基若
しくは脂環式の二塩基酸残基を、Rは同一又は異なって
もよい炭素数1〜15のアルキル基を、Eは炭素数2〜
4のアルキレン基を其々表し、mは1〜7の整数であ
り、nは0〜7の整数である)5〜300重量部、マス
ターバッチ原料が10重量部以上よりなる合成樹脂用マ
スターバッチ組成物。
An ester compound having at least one ether bond represented by the following general formula containing 0.1 to 5.0% by weight of a perchlorate based on 100 parts by weight of a synthetic resin. (Wherein X represents an alkyl group having 2 to 12 carbon atoms, an aromatic group or an alicyclic dibasic acid residue, R represents an alkyl group having 1 to 15 carbon atoms which may be the same or different, and E represents 2 carbon atoms
4 represents an alkylene group, m represents an integer of 1 to 7, and n represents an integer of 0 to 7) 5 to 300 parts by weight, and a masterbatch for synthetic resin comprising a masterbatch raw material of 10 parts by weight or more. Composition.
【請求項2】合成樹脂が熱可塑性ポリオレフィン系樹脂
であることを特徴とする請求項1記載の合成樹脂用マス
ターバッチ組成物。
2. The masterbatch composition for a synthetic resin according to claim 1, wherein the synthetic resin is a thermoplastic polyolefin resin.
【請求項3】マスターバッチ原料が各種プロセス安定
剤、染料、顔料、帯電防止剤、アンチブロッキング剤、
無機系充填剤、有機系充填剤であることを特徴とする請
求項1の記載の合成樹脂用マスターバッチ組成物。
3. The master batch raw material contains various process stabilizers, dyes, pigments, antistatic agents, anti-blocking agents,
The masterbatch composition for a synthetic resin according to claim 1, which is an inorganic filler or an organic filler.
JP11272874A 1999-08-23 1999-08-23 Master batch composition Pending JP2001059026A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11272874A JP2001059026A (en) 1999-08-23 1999-08-23 Master batch composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11272874A JP2001059026A (en) 1999-08-23 1999-08-23 Master batch composition

Publications (1)

Publication Number Publication Date
JP2001059026A true JP2001059026A (en) 2001-03-06

Family

ID=17519974

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11272874A Pending JP2001059026A (en) 1999-08-23 1999-08-23 Master batch composition

Country Status (1)

Country Link
JP (1) JP2001059026A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002309097A (en) * 2000-07-06 2002-10-23 Riken Technos Corp Antistatic resin composition
JP2014506940A (en) * 2010-12-21 2014-03-20 カラーマトリックス ホールディングス インコーポレイテッド Polymer material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002309097A (en) * 2000-07-06 2002-10-23 Riken Technos Corp Antistatic resin composition
JP2014506940A (en) * 2010-12-21 2014-03-20 カラーマトリックス ホールディングス インコーポレイテッド Polymer material
US10053545B2 (en) 2010-12-21 2018-08-21 Colormatrix Holdings, Inc. Polymeric materials

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