JPH0786180B2 - Method for producing colorant for plastics - Google Patents
Method for producing colorant for plasticsInfo
- Publication number
- JPH0786180B2 JPH0786180B2 JP63328996A JP32899688A JPH0786180B2 JP H0786180 B2 JPH0786180 B2 JP H0786180B2 JP 63328996 A JP63328996 A JP 63328996A JP 32899688 A JP32899688 A JP 32899688A JP H0786180 B2 JPH0786180 B2 JP H0786180B2
- Authority
- JP
- Japan
- Prior art keywords
- pigment
- resin
- plastics
- aqueous
- colorant
- 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.)
- Expired - Lifetime
Links
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- Compositions Of Macromolecular Compounds (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明はプラスチック用着色剤の製造方法に関し、更に
詳しくは顔料の分散性に優れた高濃度プラスチック用着
色剤の提供を目的としている。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for producing a coloring agent for plastics, and more specifically, an object thereof is to provide a coloring agent for high-concentration plastics having excellent dispersibility of a pigment.
(従来の技術及びその問題点) 従来プラスチック用着色剤としては顔料を分散剤と混合
したドライカラー、顔料を担体樹脂と高濃度に混練した
マスターバッチ等が広く使用されている。(Prior art and its problems) Conventionally, as a colorant for plastics, a dry color in which a pigment is mixed with a dispersant, a masterbatch in which a pigment is kneaded with a carrier resin in a high concentration, and the like are widely used.
これらのプラスチック用着色剤は、顔料粉末と分散剤又
は担持樹脂とをロール、ニーダー、押出機等の高剪断機
により溶融混練して顔料の分散を図っているが、一旦乾
燥した顔料粉末は粗大な二次凝集粒子が多数存在するた
め、これらの粗大粒子を全て数μm以下にまで再分散さ
せるのは非常に困難である。特に有機顔料の場合には顔
料の吸油量が大であるため高濃度微分散が困難である。
従来のプラスチックの着色においては粗大粒子の存在は
勿論無いことが好ましいが、それ程厳格には微分散が要
求されなかった。These plastic colorants are prepared by dispersing the pigment powder by melting and kneading the pigment powder and a dispersant or a supporting resin with a high shearing machine such as a roll, a kneader or an extruder, but the pigment powder once dried is coarse. Since a large number of such secondary agglomerated particles are present, it is very difficult to redisperse all of these coarse particles to a size of several μm or less. Particularly in the case of organic pigments, it is difficult to perform high-concentration fine dispersion because the oil absorption of the pigment is large.
In the conventional coloring of plastics, it is preferable that no coarse particles are present, but fine dispersion is not required so strictly.
これに対して近年に至ってはプラスチックの着色におい
ても顔料の高濃度化及び高分散性が強く要求される様に
なり、従来の粉体顔料を用いる方法では対応が困難とな
りつつある。On the other hand, in recent years, there has been a strong demand for high concentration and high dispersibility of pigments even in coloring plastics, and it is becoming difficult for conventional methods using powder pigments to cope with this.
従って本発明の目的は顔料が高濃度に分散したプラスチ
ック用着色剤を提供することである。Therefore, an object of the present invention is to provide a colorant for plastics in which a pigment is dispersed in a high concentration.
(問題点を解決するための手段) 上記目的は以下の本発明によって達成される。(Means for Solving Problems) The above object is achieved by the present invention described below.
すなわち、本発明は、顔料の水性ペーストと樹脂溶液と
を混練して水性相の顔料を樹脂溶液相に移行させ、しか
る後に水及び有機溶剤を除去することを特徴とするプラ
スチック用着色剤の製造方法である。That is, the present invention is a method for producing a colorant for plastics, which comprises kneading an aqueous pigment paste and a resin solution to transfer an aqueous phase pigment to a resin solution phase, and then removing water and an organic solvent. Is the way.
(作用) 二次凝集していない顔料の水性ペーストから、顔料の粉
末化工程を経ることなく、顔料を水相から樹脂相に移行
させることによって、粗大粒子を含有しないプラスチッ
ク用着色剤が提供される。(Function) A pigment coloring agent for plastics containing no coarse particles is provided by transferring the pigment from the aqueous phase to the resin phase from the aqueous paste of the pigment which is not secondarily aggregated, without going through the powdering step of the pigment. It
(好ましい実施態様) 次に好ましい実施態様を挙げて本発明を更に具体的に説
明する。(Preferred Embodiment) Next, the present invention will be described more specifically with reference to preferred embodiments.
本発明で使用する顔料の水性ペーストとは、顔料を水相
中で製造し、その後、乾燥することなく濾過して得た水
性ペーストである。このようなペースト状の顔料は乾燥
工程を経ることがないので、顔料粒子は二次凝集するこ
となく一次粒子のままで殆どの場合に10μmを越える粒
子は含有していない。The aqueous paste of the pigment used in the present invention is an aqueous paste obtained by producing the pigment in an aqueous phase and then filtering it without drying. Since such a pasty pigment does not undergo a drying step, the pigment particles do not secondary aggregate and remain as primary particles in most cases, and do not contain particles having a size of more than 10 μm.
本発明で使用する顔料としてはアゾ顔料、フタロシアニ
ン顔料、キナクリドン顔料、カーボンブラック顔料等従
来公知の顔料はいずれも使用でき、特に親油性の高い有
機顔料が好ましい。顔料の水性ペースト中の固形分は特
に限定されないが、固形分が低すぎると工程的に不経済
であり、又、固形分が高すぎると表面で乾燥が生じて二
次凝集粒子が生じる恐れがあり、従って好ましい固形分
の範囲は25乃至80重量%の濃度である。As the pigment used in the present invention, any conventionally known pigment such as an azo pigment, a phthalocyanine pigment, a quinacridone pigment and a carbon black pigment can be used, and an organic pigment having high lipophilicity is particularly preferable. The solid content in the aqueous paste of the pigment is not particularly limited, but if the solid content is too low, it is uneconomical in the process, and if the solid content is too high, drying may occur on the surface to cause secondary agglomerated particles. Thus, the preferred solids range is a concentration of 25 to 80% by weight.
本発明において使用する樹脂としては従来顔料の分散剤
として使用されている樹脂分散剤やマスターバッチの担
体樹脂として使用されている樹脂がいずれも使用するこ
とができる。例えば、分散剤としては低分子量ポリエチ
レン、低分子量ポリプロピレン、各種ワックス等が使用
でき、又、樹脂としてはアクリル樹脂、スチレン樹脂、
アクリル−スチレン樹脂、ポリエステル樹脂、フェノー
ル樹脂、ロジン変性マレイン酸樹脂、石油樹脂、エポキ
シ樹脂、ABS樹脂、ポリカーボネート樹脂、ポリ塩化ビ
ニル樹脂、ポリ酢酸ビニル樹脂、アルキド樹脂等が挙げ
られる。As the resin used in the present invention, any of the resin dispersants conventionally used as a dispersant for pigments and the resins used as a carrier resin for a masterbatch can be used. For example, as the dispersant, low molecular weight polyethylene, low molecular weight polypropylene, various waxes, etc. can be used, and as the resin, acrylic resin, styrene resin,
Examples thereof include acrylic-styrene resin, polyester resin, phenol resin, rosin-modified maleic acid resin, petroleum resin, epoxy resin, ABS resin, polycarbonate resin, polyvinyl chloride resin, polyvinyl acetate resin, and alkyd resin.
本発明方法は、上記の如き顔料の水性ペーストと上記の
如き樹脂の溶液とをフラッシャーの如き混練機中で混練
して、水相中の顔料を樹脂溶液中に移行させる方法であ
り、使用する有機溶剤としては、トルエン、キシレン等
の水と混和しない有機溶剤を用いる。有機溶剤の使用量
は樹脂が液化するのに必要な量であり、樹脂濃度が10乃
至90%程度になる割合で使用するのが一般的である。フ
ラッシャー中での混練は常温で行ってもよいが、通常は
加熱しなくともフラッシャー内の摩擦力により50乃至80
℃程度に上昇する。混練時の温度は常温乃至130℃程度
であり、水の沸点以上の温度で行う場合には密閉式の加
圧フラッシャーを使用するのが好ましい。The method of the present invention is a method in which an aqueous paste of a pigment as described above and a solution of a resin as described above are kneaded in a kneader such as a flasher to transfer the pigment in the aqueous phase into the resin solution, which is used. As the organic solvent, an organic solvent immiscible with water such as toluene or xylene is used. The amount of the organic solvent used is the amount necessary for the resin to liquefy, and is generally used in such a ratio that the resin concentration becomes about 10 to 90%. The kneading in the flasher may be performed at room temperature, but usually 50 to 80 due to the frictional force in the flasher without heating.
It rises to about ℃. The temperature at the time of kneading is from room temperature to about 130 ° C., and when the temperature is higher than the boiling point of water, it is preferable to use a closed pressure flasher.
フラッシャーに添加する顔料の水性ペースト及び樹脂溶
液の混合比は顔料の水性ペーストの固形分、樹脂溶液の
濃度等によって変化するが、得られるプラスチック用着
色剤の顔料濃度が20乃至80重量%になる割合が好まし
い。The mixing ratio of the pigment aqueous paste and the resin solution added to the flasher varies depending on the solid content of the pigment aqueous paste, the concentration of the resin solution, etc., but the pigment concentration of the obtained plastic colorant is 20 to 80% by weight. Ratios are preferred.
フラッシングに際してはフラッシャーの容量一杯に顔料
の水性ペーストと樹脂溶液とをチャージしてもよいが、
好ましい方法はチャージを数回に分けて行う方法であ
る。すなわち、1回目のチャージにおいてフラッシャー
の容量の約1/5乃至1/2程度の容積に両者をチャージして
フラッシングを行い、分離した水を排出し、次いで同様
の量のチャージを行い、フラッシングした後水を排出す
る。このように分離した水を排出しながら行うことによ
ってフラッシング効率を著しく高めることができる。At the time of flushing, the pigment aqueous paste and the resin solution may be charged to the full capacity of the flasher,
A preferred method is a method in which the charge is divided into several times. That is, in the first charge, both were charged to a volume of about 1/5 to 1/2 of the capacity of the flasher to perform flushing, the separated water was discharged, and then the same amount of charge was performed to perform flushing. Drain the after water. The flushing efficiency can be remarkably improved by discharging the separated water as described above.
最後のフラッシングが完了したら、残留している水を除
去し、好ましくは減圧下で残留水と有機溶剤を除去する
ことによって所望のプラスチック用着色剤が得られる。After the final flushing is complete, the residual water is removed, preferably under reduced pressure, to remove the residual water and organic solvent to give the desired plastic colorant.
(効果) 以上の如き本発明によれば、二次凝集していない顔料の
水性ペーストから、顔料の粉末化工程を経ることなく、
顔料を水相から樹脂相に移行させることによって、粗大
粒子を含有しないプラスチック用着色剤が提供される。(Effect) According to the present invention as described above, an aqueous paste of a pigment that has not been secondarily aggregated can be used without a powdering step of the pigment.
Transferring the pigment from the aqueous phase to the resin phase provides a plastic colorant that does not contain coarse particles.
(実施例) 次に実施例を挙げて本発明を更に具体的に説明する。
尚、文中、部又は%とあるのは特に断りのない限り重量
基準である。(Example) Next, an Example is given and this invention is demonstrated still more concretely.
In the text, parts and% are based on weight unless otherwise specified.
実施例1 ジメチルキナクリドン顔料の水性ペースト(固形分30
%)180部とアクリルスチレン樹脂(三洋化成社製)の6
0%キシレン溶液75部をフラッシャーに入れ、常温で35
分間混練して分離した水を排出した。次に前記顔料の水
性ペースト120部及び同樹脂溶液50部を追加し、常温で3
5分間混練し、分離した水を排出した。更に同樹脂溶液3
75部を追加して常温で30分間混練して分離した水を排出
した。最後にフラッシャーを70cmHgに減圧して125℃で
2.5時間混練後、冷却して粉末状の本発明のプラスチッ
ク用着色剤を得た。Example 1 Aqueous paste of dimethylquinacridone pigment (solid content 30
%) 180 parts and 6 of acrylic styrene resin (manufactured by Sanyo Chemical Co., Ltd.)
Add 75 parts of 0% xylene solution to the flasher and keep at room temperature for 35
The separated water was discharged after kneading for a minute. Next, add 120 parts of the above-mentioned pigment aqueous paste and 50 parts of the same resin solution, and
The mixture was kneaded for 5 minutes, and the separated water was discharged. Furthermore, the same resin solution 3
After adding 75 parts, the mixture was kneaded at room temperature for 30 minutes, and the separated water was discharged. Finally, depressurize the flasher to 70 cmHg at 125 ° C.
After kneading for 2.5 hours, the mixture was cooled to obtain a powdery colorant for plastics of the present invention.
上記着色剤をトルエンに溶解して光学顕微鏡(400倍)
で顔料の分散性を調べたところ、8μm以上の粗大粒子
は認められなかった。Optical microscope (400x) by dissolving the above colorants in toluene
When the dispersibility of the pigment was examined with, no coarse particles of 8 μm or more were observed.
実施例2 ポリスチレン樹脂(エッソ社製、ピコラスチックD−12
5)の50%トルエン溶液4,200部をフラッシャーに入れ、
続いてシアニングリーンの水性プレスケーキ(固形分42
%)1,550部を投入し、60分間良く撹拌した。分離した
水分をデカンテーションにより除去した後、更に30分間
混練を行った。その後加熱減圧下(130℃、70cmHg)で
2時間混練を行いながら水及び溶剤を除去した。その後
冷却及び粉砕して緑色の本発明のペレット状プラスチッ
ク用着色剤を得た。Example 2 Polystyrene resin (Picolastic D-12 manufactured by Esso Co., Ltd.
Put 4200 parts of 50% toluene solution of 5) into the flasher,
Next, cyanine green aqueous press cake (solid content 42
%) 1,550 parts were added and well stirred for 60 minutes. After removing the separated water by decantation, kneading was further performed for 30 minutes. After that, water and solvent were removed while kneading under heating and reduced pressure (130 ° C., 70 cmHg) for 2 hours. Then, the mixture was cooled and pulverized to obtain a green colorant for plastic pellets of the present invention.
上記着色剤をトルエンに溶解して光学顕微鏡(400倍)
で顔料の分散性を調べたところ、10μm以上の粗大粒子
は認められなかった。Optical microscope (400x) by dissolving the above colorants in toluene
When the dispersibility of the pigment was examined by means of the above, no coarse particles of 10 μm or more were observed.
実施例3 ポリアクリル樹脂(旭化成社製、スタイロン666)の60
%トルエン溶液1,500部をフラッシャーに入れ、続いて
ジスアゾイエローの水性プレスケーキ(固形分35%)2,
000部を投入し、45分間良く撹拌した。分離した水分を
デカンテーションにより除去した後、その後更に同じ樹
脂溶液1,500部を追加し、更に同じプレスケーキ1,400部
を投入した。続けて45分間良く混練後、分離した水を除
去し、更に30分間混練を行った。その後加熱減圧下(18
0℃、70cmHg)で2.5時間混練を行いながら水及び溶剤を
除去した。その後直ちに押出機を通して黄色の本発明の
ペレット状プラスチック用着色剤を得た。Example 3 60 of polyacrylic resin (manufactured by Asahi Kasei, Styron 666)
% 1,500 parts toluene solution into a flasher, followed by disazo yellow aqueous presscake (35% solids) 2,
000 parts was added and well stirred for 45 minutes. After removing the separated water by decantation, 1,500 parts of the same resin solution was further added, and 1,400 parts of the same press cake was further added. Subsequently, the mixture was thoroughly kneaded for 45 minutes, the separated water was removed, and the mixture was further kneaded for 30 minutes. After that, under heating and reduced pressure (18
Water and solvent were removed while kneading at 0 ° C. and 70 cmHg) for 2.5 hours. Immediately thereafter, a yellow coloring agent for plastics of the present invention was obtained through an extruder.
上記着色剤をトルエンに溶解して光学顕微鏡(400倍)
で顔料の分散性を調べたところ、5μm以上の粗大粒子
は認められなかった。Optical microscope (400x) by dissolving the above colorants in toluene
When the dispersibility of the pigment was examined with, no coarse particles of 5 μm or more were observed.
Claims (2)
て水性相の顔料を樹脂溶液相に移行させ、しかる後に水
及び有機溶剤を除去することを特徴とするプラスチック
用着色剤の製造方法。1. A method for producing a colorant for plastics, which comprises kneading an aqueous paste of a pigment and a resin solution to transfer an aqueous phase pigment to a resin solution phase, and then removing water and an organic solvent. .
加する請求項1に記載の方法。2. The method according to claim 1, wherein the aqueous pigment paste and the resin solution are sequentially added.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63328996A JPH0786180B2 (en) | 1988-12-28 | 1988-12-28 | Method for producing colorant for plastics |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63328996A JPH0786180B2 (en) | 1988-12-28 | 1988-12-28 | Method for producing colorant for plastics |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02175768A JPH02175768A (en) | 1990-07-09 |
| JPH0786180B2 true JPH0786180B2 (en) | 1995-09-20 |
Family
ID=18216440
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63328996A Expired - Lifetime JPH0786180B2 (en) | 1988-12-28 | 1988-12-28 | Method for producing colorant for plastics |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0786180B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009242527A (en) * | 2008-03-31 | 2009-10-22 | Sumika Color Kk | Method for producing organic pigment composition |
| JP2025078318A (en) * | 2023-11-08 | 2025-05-20 | 東洋アルミニウム株式会社 | Effect pigment preparation, thermoplastic composition containing the effect pigment preparation and method for producing a paint or ink containing the effect pigment preparation - Patents.com |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS547288A (en) * | 1977-06-20 | 1979-01-19 | Hitachi Ltd | Observation window for sealed container |
| JPS6031857A (en) * | 1983-08-01 | 1985-02-18 | Dai Ichi High Frequency Co Ltd | Narrow mouth container having resing lining formed to its inner surface and its preparation |
| JPS6361349A (en) * | 1986-09-01 | 1988-03-17 | Pfu Ltd | Interface control method |
-
1988
- 1988-12-28 JP JP63328996A patent/JPH0786180B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02175768A (en) | 1990-07-09 |
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