JPS631884B2 - - Google Patents
Info
- Publication number
- JPS631884B2 JPS631884B2 JP18033881A JP18033881A JPS631884B2 JP S631884 B2 JPS631884 B2 JP S631884B2 JP 18033881 A JP18033881 A JP 18033881A JP 18033881 A JP18033881 A JP 18033881A JP S631884 B2 JPS631884 B2 JP S631884B2
- Authority
- JP
- Japan
- Prior art keywords
- pigment
- waste ink
- solvent
- pigments
- 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.)
- Expired
Links
Landscapes
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Extraction Or Liquid Replacement (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Description
本発明は廃インキから顔料を回収する方法に関
する。
凸版、凹版、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 in various types of printing, such as letterpress, intaglio, 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
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、前記の顔料の種類および
介在樹脂の種類によつて顔料分散性に選択性を示
す溶剤について検討を進めたところ、この溶剤の
うちエステル類は、前記したように介在樹脂に対
して良好な溶解性を示し、しかも色のくすみの原
因となるフタロシアニンブルーやカーボンブラツ
クはこの介在樹脂との結びつきが強いため、該樹
脂の溶解に伴なつて溶剤側へ分散するという知見
を得た。
従つて、廃インキをエステル類で処理すれば、
廃インキ中の樹脂と共にフタロシアニンブルーや
カーボンブラツクが溶剤側に移行し、他の色相の
鮮やかな顔料は表2に示す通りエステル類に対し
て分散性が悪いので沈降し、分離、回収できる。
本発明は、この点に基づいて完成されたもの
で、廃インキにエステル類を加えた後、遠心分離
することを特徴とする廃インキからの顔料回収法
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にエステル類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。な
お、この遠心分離に先立つてデカンテーシヨンす
ることもできる。固相6には顔料、液相7には溶
剤が回収される。
ここでエステル類2としては、前述したよう
に、酢酸メチル、酢酸エチル、酢酸ブチル等が使
用できる。
また廃インキ1とエステル類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
廃インキ20mlに酢酸エチル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、上記酢酸エチルの代りに酢酸メチルある
いは酢酸ブチル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] △ 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. For example, methyl alcohol, ethyl alcohol: If the intervening resin is an alkyd resin, these alcohols have no effect of dissolving the alkyd resin, so regardless of the type of pigment, the dispersibility is poor. In the case of cellulose, these alcohols dissolve nitrocellulose, so they show the same dispersibility as shown in Table 2. Isopropyl alcohol: Regardless of whether the intervening resin is an alkyd resin or nitrocellulose, isopropyl alcohol dissolves these resins. Ethyl acetate: Regardless of whether the intervening resin is an alkyd resin or nitrocellulose, ethyl acetate has the effect of dissolving these resins, so the dispersibility is poor regardless of the type of pigment. Shows similar dispersibility, and shows selectivity in dispersion. (4) Blue pigments (phthalocyanine blue) and carbon black tend to be somewhat easily dispersed in any solvent. Based on the above knowledge, the present inventors first added a solvent with poor pigment dispersibility, or a mixture of the solvent with a solvent with good pigment dispersibility, alcohol, etc. to the waste ink to form pigment particles. We proposed a method to recover the pigment and the solvent by coagulation and sedimentation separation. The present inventors further investigated solvents that exhibit selectivity in pigment dispersibility depending on the type of pigment and the type of intervening resin, and found that among these solvents, esters do not interfere with the intervening resin as described above. Knowledge that phthalocyanine blue and carbon black, which exhibit good solubility in resins and cause dullness of color, have a strong bond with this intervening resin, and are therefore dispersed into the solvent as the resin dissolves. I got it. Therefore, if waste ink is treated with esters,
Phthalocyanine blue and carbon black migrate to the solvent side together with the resin in the waste ink, and as shown in Table 2, pigments with bright hues have poor dispersibility with respect to esters, so they settle, and can be separated and recovered. The present invention has been completed based on this point, and relates to a method for recovering pigments from waste ink, which is characterized by adding esters to waste ink and then centrifuging the mixture. FIG. 2 is a flow sheet showing an embodiment of the method of the present invention. In FIG. 2, esters 2 are added to waste ink 1 and mixed 3, followed by vigorous stirring 4. Next, this liquid is centrifuged 5 to separate solid and liquid. Incidentally, decantation can also be performed prior to this centrifugation. The pigment is recovered in the solid phase 6 and the solvent is recovered in the liquid phase 7. Here, as the esters 2, as mentioned above, methyl acetate, ethyl acetate, butyl acetate, etc. can be used. Furthermore, the mixing ratio of waste ink 1 and esters 2 is determined by the solvent/waste ink ratio (volume ratio), as is clear from the relationship between the pigment separation rate and the solvent/waste ink ratio (volume ratio) during pigment recovery shown in Figure 3. 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 100 ml of ethyl acetate was added to 20 ml of waste ink, the centrifuge 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 85-90% could be obtained. When the same test as above was conducted using methyl acetate or butyl acetate instead of ethyl acetate, almost the same results as above were obtained.
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例
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 in pigment recovery. It is a figure showing the relationship with ink ratio (capacity ratio).
Claims (1)
することを特徴とする廃インキからの顔料回収
法。1. A method for recovering pigments from waste ink, which is characterized by adding esters to waste ink and then centrifuging it.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18033881A JPS5881411A (en) | 1981-11-12 | 1981-11-12 | Pigment recovery method from waste ink |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18033881A JPS5881411A (en) | 1981-11-12 | 1981-11-12 | Pigment recovery method from waste ink |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5881411A JPS5881411A (en) | 1983-05-16 |
| JPS631884B2 true JPS631884B2 (en) | 1988-01-14 |
Family
ID=16081468
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18033881A Granted JPS5881411A (en) | 1981-11-12 | 1981-11-12 | Pigment recovery method from waste ink |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5881411A (en) |
-
1981
- 1981-11-12 JP JP18033881A patent/JPS5881411A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5881411A (en) | 1983-05-16 |
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