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JPS633642B2 - - Google Patents
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JPS633642B2 - - Google Patents

Info

Publication number
JPS633642B2
JPS633642B2 JP18033981A JP18033981A JPS633642B2 JP S633642 B2 JPS633642 B2 JP S633642B2 JP 18033981 A JP18033981 A JP 18033981A JP 18033981 A JP18033981 A JP 18033981A JP S633642 B2 JPS633642 B2 JP S633642B2
Authority
JP
Japan
Prior art keywords
pigment
solvent
dispersibility
waste ink
pigments
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
Application number
JP18033981A
Other languages
Japanese (ja)
Other versions
JPS5881412A (en
Inventor
Masataka Mizutani
Toshihiko Kashiwai
Masaki Minemoto
Kazuo Sakanaya
Hayami Nagano
Masashi Hirao
Atsushi Kametaka
Masato Yamaguchi
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.)
Dai Nippon Printing Co Ltd
Mitsubishi Heavy Industries Ltd
Original Assignee
Dai Nippon Printing Co Ltd
Mitsubishi Heavy Industries Ltd
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 Dai Nippon Printing Co Ltd, Mitsubishi Heavy Industries Ltd filed Critical Dai Nippon Printing Co Ltd
Priority to JP18033981A priority Critical patent/JPS5881412A/en
Publication of JPS5881412A publication Critical patent/JPS5881412A/en
Publication of JPS633642B2 publication Critical patent/JPS633642B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Separation Of Suspended Particles By Flocculating Agents (AREA)
  • Extraction Or Liquid Replacement (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は廃インキから顔料を回収する方法に関
する。 凸板、凹板、オフセツト、グラビア等各種の印
刷に適用されるインキは、一般に、顔料、樹脂、
溶剤、可塑剤等の添加剤からなり、第1図に模式
的に示すように、顔料粒子1が樹脂2を介在して
溶剤3中に均一に分散しているものと考えられ
る。 この顔料粒子は、体質顔料、無機系顔料、有機
系顔料に大別され、それぞれ表1に示すような物
性を有している。
The present invention relates to a method for recovering pigment from waste ink. Inks used for various types of printing, such as convex, concave, offset, and gravure, generally contain pigments, resins,
It consists of additives such as a solvent and a plasticizer, and as schematically shown in FIG. 1, it is thought that pigment particles 1 are uniformly dispersed in a solvent 3 with a resin 2 interposed therebetween. These pigment particles are broadly classified into extender pigments, inorganic pigments, and organic pigments, each of which has physical properties as shown in Table 1.

【表】【table】

【表】 なお、溶剤、樹脂、可塑剤等の添加剤は、上記
の顔料の種類に応じて適切なものが使用されるこ
とはいうまでもない。 新品インキの色相は、大別して赤、青、黄、白
および黒系統であり、用途に応じて単独もしくは
二色以上を混合して用いる。 ところで、色が黒くくすんで使用できなくなつ
たインキや、印刷機等を洗浄したあとの廃液は、
廃インキとしてインキ製造工程や印刷工場等から
大量に排出され、いずれの廃インキも各色相のイ
ンキが混合したものであつて、色のくすんだ廃イ
ンキ中にはカーボンブラツクからなる黒インキ
や、フタロシアニンブルーからなる青インキが含
まれている。 上記の廃インキから顔料、溶剤等の有価物を回
収することは困難で、従来は、殆んどが焼却ある
いは投棄され、まれに廃インキ中に熱風、蒸気等
を注入して溶剤を放散させ、凝縮器等により回収
することもあつたが、充分な回収を行うことはで
きなかつた。 本発明者等は、廃インキから顔料や溶剤等の有
価物を回収し、しかも回収顔料の再利用度を高め
るべく、色のくすみの原因となるカーボンブラツ
クや青色顔料(フタロシアニンブルー)を除去
し、赤、黄、茶色等の色相の鮮やかな顔料を回収
する方法について研究を重ねた結果、次のような
知見を得た。 先ず、表1に示したインキに使用される顔料粒
子は、表2に示すように溶剤の種類によつて異な
つた分散性を示すこと。
[Table] It goes without saying that appropriate additives such as solvents, resins, and plasticizers are used depending on the type of pigment mentioned above. The hues of new inks are broadly classified into red, blue, yellow, white, and black, and depending on the purpose, they are used alone or in combination of two or more colors. By the way, ink that has become black and dull and can no longer be used, as well as waste liquid after cleaning printing machines, etc.
A large amount of waste ink is discharged from ink manufacturing processes, printing factories, etc., and each waste ink is a mixture of inks of various hues, and the dull colored waste ink includes black ink made of carbon black, Contains blue ink consisting of phthalocyanine blue. It is difficult to recover valuable materials such as pigments and solvents from the above waste ink, and conventionally, most of it has been incinerated or dumped, and in rare cases, hot air, steam, etc. have been injected into the waste ink to dissipate the solvent. , recovery using a condenser or the like was possible, but sufficient recovery could not be achieved. The present inventors recovered valuable materials such as pigments and solvents from waste ink, and in order to increase the degree of reuse of the recovered pigments, we removed carbon black and blue pigments (phthalocyanine blue) that cause dull colors. As a result of repeated research on methods for recovering pigments with vivid hues such as red, yellow, and brown, the following findings were obtained. First, the pigment particles used in the inks shown in Table 1 show different dispersibility depending on the type of solvent, as shown in Table 2.

【表】 △ 分散性やや良
× 分散性悪
次に、前記したように顔料粒子をインキに使用
する際には樹脂(第1図中の2)を介在させる
が、この樹脂の種類によつても、表2の分散性は
次のように異なつてくること。 (1) トルエン、キシレン等の芳香族炭化水素は、
表2に示すようにいずれの顔料も分散せず、沈
降する傾向にあり、しかも介在樹脂の種類にか
かわらず、この傾向は変わらない。 (2) メチルセロソルブ等のエーテル類、シクロヘ
キサノン等のケトン類は表2に示すようにいず
れの顔料も良く分散し、しかも介在樹脂の種類
にかかわらず、この傾向は変わらない。 (3) 酢酸エチル等のエステル類、メチルアルコー
ル、エチルアルコール、イソプロピルアルコー
ル等のアルコール類は、表2に示すように顔料
の種類によつて分散性に選択性を示し、しかも
介在樹脂の種類によつても、例えば、 メチルアルコール、エチルアルコール:介在樹
脂がアルキツド樹脂の場合、これらのアルコ
ールはアルキツド樹脂を溶解する作用がない
ため、顔料の種類にかかわらず、分散性は悪
い。介在樹脂がニトロセルロースの場合は、
これらのアルコールはニトロセルロースを溶
解する作用があるため、表2と同様の分散性
を示す。 イソプロピルアルコール:介在樹脂がアルキツ
ド樹脂、ニトロセルロースいずれの場合も、
イソプロピルアルコールはこれらの樹脂を溶
解する作用がないため、顔料の種類にかかわ
らず分散性は悪い、 酢酸エチル:介在樹脂がアルキツド樹脂、ニト
ロセルロースいずれの場合も、酢酸エチルは
これらの樹脂を溶解する作用があるため、表
2と同様の分散性を示す、 のように分散性に選択性を示す。 (4) 青色顔料(フタロシアニンブルー)およびカ
ーボンブラツクは、いずれの溶剤にもやや分散
し易い傾向がある。 以上の知見に基づいて本発明者等は、先に廃イ
ンキに顔料分散性の悪い溶剤、あるいは該溶剤に
顔料分散性の良い溶剤やアルコール類等を混合さ
せたものを添加して顔料粒子を凝集沈降分離さ
せ、顔料を回収すると共に溶剤を回収する方法を
提案した。 本発明者等は、更に、顔料分散性の良い溶剤の
みで処理しても顔料が回収できるのではないかと
の観点に立ち、検討を進めたところ、表2に示す
顔料の溶剤への分散性は、顔料分散性の良い溶剤
中では表2′のようになること、すなわち色のくす
みの原因となるフタロシアニンブルーやカーボン
ブラツクに対して非常に良好な顔料分散性を示す
ことを確認した。これは、顔料分散性の良い溶剤
は、前記した介在樹脂に対して溶解性を示して該
樹脂を溶剤側に移行させ、上記のフタロシアニン
ブルーやカーボンブラツクはこの樹脂との結びつ
きが強いため、樹脂と共に溶剤側へ分散すること
によるものと考えられる。
[Table] △ Slightly good dispersibility × Poor dispersibility Next, as mentioned above, when pigment particles are used in ink, a resin (2 in Figure 1) is used, but depending on the type of resin, , the dispersion properties in Table 2 differ as follows. (1) Aromatic hydrocarbons such as toluene and xylene are
As shown in Table 2, none of the pigments is dispersed and tends to settle, and this tendency does not change regardless of the type of intervening resin. (2) As shown in Table 2, ethers such as methyl cellosolve and ketones such as cyclohexanone disperse well in all pigments, and this tendency does not change regardless of the type of intervening resin. (3) As shown in Table 2, esters such as ethyl acetate, alcohols such as methyl alcohol, ethyl alcohol, and isopropyl alcohol exhibit selectivity in dispersibility depending on the type of pigment, and also depending on the type of intervening resin. Even so, for example, methyl alcohol, ethyl alcohol: When the intervening resin is an alkyd resin, these alcohols have no effect of dissolving the alkyd resin, so the dispersibility is poor regardless of the type of pigment. If the intervening resin is nitrocellulose,
Since these alcohols have the effect of dissolving nitrocellulose, they exhibit the same dispersibility as shown in Table 2. Isopropyl alcohol: Regardless of whether the intervening resin is alkyd resin or nitrocellulose,
Isopropyl alcohol has no effect of dissolving these resins, so it has poor dispersibility regardless of the type of pigment. Ethyl acetate: Ethyl acetate dissolves these resins, whether the intervening resin is alkyd resin or nitrocellulose. Because of this effect, it shows dispersibility similar to that shown in Table 2, and shows selectivity in dispersion as shown in Table 2. (4) Blue pigments (phthalocyanine blue) and carbon black tend to be somewhat easily dispersed in any solvent. Based on the above findings, the present inventors first added to the waste ink a solvent with poor pigment dispersibility, or a mixture of the solvent with a solvent with good pigment dispersibility, alcohol, etc. to form pigment particles. We proposed a method to recover the pigment and the solvent through coagulation and sedimentation separation. The inventors of the present invention further considered that the pigment could be recovered even if treated only with a solvent with good pigment dispersibility, and as a result of further investigation, the dispersibility of the pigment in the solvent shown in Table 2 was found. It was confirmed that in a solvent with good pigment dispersibility, the results are as shown in Table 2', that is, it shows very good pigment dispersibility against phthalocyanine blue and carbon black, which cause dull colors. This is because a solvent with good pigment dispersibility exhibits solubility in the intervening resin mentioned above and transfers the resin to the solvent side, and the above-mentioned phthalocyanine blue and carbon black have a strong bond with this resin. This is thought to be due to the dispersion to the solvent side.

【表】 従つて、廃インキを顔料分散性の良い溶剤のみ
で処理すれば、色のくすみの原因となるフタロシ
アニンブルーやカーボンブラツクは凝集沈降せず
に溶剤側に残り、他の色相の鮮やかな顔料が凝集
沈降すると共に、介在樹脂や添加剤等も溶解して
溶剤側に移行し、かなりの高純度で色相の鮮やか
な顔料が回収できることが確認できた。 本発明は、この点に基づいて完成されたもの
で、廃インキに顔料分散性の良い溶剤を加えた
後、遠心分離することを特徴とする廃インキから
顔料を回収する方法に関するものである。 第2図は本発明方法の一実施態様例を示すフロ
ーシートである。 第2図において、廃インキ1に顔料分散性の良
い溶剤2を添加混合3したのち、激しく撹拌4す
る。つぎに、この液を遠心分離5して固液分離す
る。この遠心分離の前にデカンテーシヨンを行う
こともできる。固相6には顔料、液相7には溶剤
が回収される。 ここで顔料分散性の良い溶剤2としては、前述
したように、シクロヘキサノン、メチルイソブチ
ルケトン等のケトン類、メチルセロソルブ等のエ
ーテル類等が使用される。 また廃インキ1と顔料分散性の良い溶剤2との
混合割合は、第3図に示す顔料回収における顔料
分離率と溶剤/廃インキ比(容量比)の関係から
明らかなように、溶剤/廃インキ比(容量比)は
2〜3以上とすることが好ましい。 以下、実施例により本発明方法を更に具体的に
説明する。 実施例 1 廃インキ20mlにシクロヘキサノン100mlを加え
て、遠心分離器にセツトし、回転数6000rpmの条
件で10分間運転して顔料を液相から分離した。こ
の結果、90〜99%純度の顔料分3.1gを得ること
ができた。 実施例 2 廃インキ20mlにメチルセロソルブ100mlを加え
て遠心分離器にセツトし、回転数6000rpmの条件
で10分間運転して顔料を液相から分離した。この
結果、純度が85〜90%の顔料分3.2gを得ること
ができた。 なお、上記以外の顔料分散性の良い溶剤を使用
して上記と同様のテストを行つた結果、上記とほ
ぼ同様の結果が得られた。
[Table] Therefore, if waste ink is treated only with a solvent that has good pigment dispersibility, phthalocyanine blue and carbon black, which cause dull colors, will not coagulate and settle but will remain in the solvent, and other vivid hues will remain. It was confirmed that as the pigment coagulated and precipitated, the intervening resin and additives were also dissolved and transferred to the solvent side, making it possible to recover pigments with fairly high purity and vivid hues. The present invention has been completed based on this point, and relates to a method for recovering pigment from waste ink, which is characterized by adding a solvent with good pigment dispersibility to waste ink and then centrifuging it. FIG. 2 is a flow sheet showing an embodiment of the method of the present invention. In FIG. 2, a solvent 2 with good pigment dispersibility is added to waste ink 1 and mixed 3 and then vigorously stirred 4. Next, this liquid is centrifuged 5 to separate solid and liquid. Decantation can also be carried out before this centrifugation. The pigment is recovered in the solid phase 6 and the solvent is recovered in the liquid phase 7. Here, as the solvent 2 having good pigment dispersibility, as mentioned above, ketones such as cyclohexanone and methyl isobutyl ketone, and ethers such as methyl cellosolve are used. In addition, the mixing ratio of waste ink 1 and solvent 2 with good pigment dispersibility is determined by The ink ratio (capacity ratio) is preferably 2 to 3 or more. Hereinafter, the method of the present invention will be explained in more detail with reference to Examples. Example 1 100 ml of cyclohexanone was added to 20 ml of waste ink, set in a centrifugal separator, and operated at a rotation speed of 6000 rpm for 10 minutes to separate the pigment from the liquid phase. As a result, 3.1 g of pigment with a purity of 90 to 99% could be obtained. Example 2 100 ml of methyl cellosolve was added to 20 ml of waste ink, the centrifugal separator was set, and the centrifugal separator was operated at a rotation speed of 6000 rpm for 10 minutes to separate the pigment from the liquid phase. As a result, 3.2 g of pigment with a purity of 85 to 90% could be obtained. In addition, as a result of conducting the same test as above using a solvent other than the above-mentioned solvent with good pigment dispersibility, almost the same results as above were obtained.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はインキ中の顔料粒子の分散状況を模式
的に示す図、第2図は本発明方法の一実施態様を
示すフローシート、第3図は顔料回収における顔
料分離率と溶剤/廃インキ比(容量比)との関係
を示す図である。
Fig. 1 is a diagram schematically showing the dispersion state of pigment particles in ink, Fig. 2 is a flow sheet showing an embodiment of the method of the present invention, and Fig. 3 is a diagram showing the pigment separation rate and solvent/waste ink during pigment recovery. It is a figure showing the relationship with ratio (capacity ratio).

Claims (1)

【特許請求の範囲】[Claims] 1 廃インキに顔料分散性の良い溶剤を加えた
後、遠心分離することを特徴とする廃インキから
顔料を回収する方法。
1. A method for recovering pigments from waste ink, which comprises adding a solvent with good pigment dispersibility to waste ink and then centrifuging the mixture.
JP18033981A 1981-11-12 1981-11-12 How to recover pigments from waste ink Granted JPS5881412A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18033981A JPS5881412A (en) 1981-11-12 1981-11-12 How to recover pigments from waste ink

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18033981A JPS5881412A (en) 1981-11-12 1981-11-12 How to recover pigments from waste ink

Publications (2)

Publication Number Publication Date
JPS5881412A JPS5881412A (en) 1983-05-16
JPS633642B2 true JPS633642B2 (en) 1988-01-25

Family

ID=16081487

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18033981A Granted JPS5881412A (en) 1981-11-12 1981-11-12 How to recover pigments from waste ink

Country Status (1)

Country Link
JP (1) JPS5881412A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5199981A (en) * 1991-01-18 1993-04-06 Sicpa Holding Sa Pigment compositions including intaglio printing ink waste

Also Published As

Publication number Publication date
JPS5881412A (en) 1983-05-16

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