JPS5923733B2 - Coloring method for expanded polystyrene particles - Google Patents

Coloring method for expanded polystyrene particles

Info

Publication number
JPS5923733B2
JPS5923733B2 JP8654382A JP8654382A JPS5923733B2 JP S5923733 B2 JPS5923733 B2 JP S5923733B2 JP 8654382 A JP8654382 A JP 8654382A JP 8654382 A JP8654382 A JP 8654382A JP S5923733 B2 JPS5923733 B2 JP S5923733B2
Authority
JP
Japan
Prior art keywords
expanded polystyrene
dye
polystyrene particles
parts
grains
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
JP8654382A
Other languages
Japanese (ja)
Other versions
JPS58204034A (en
Inventor
清 富岡
正弘 中安
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.)
Tokyo Printing Ink Mfg Co Ltd
Original Assignee
Tokyo Printing Ink Mfg Co 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 Tokyo Printing Ink Mfg Co Ltd filed Critical Tokyo Printing Ink Mfg Co Ltd
Priority to JP8654382A priority Critical patent/JPS5923733B2/en
Publication of JPS58204034A publication Critical patent/JPS58204034A/en
Publication of JPS5923733B2 publication Critical patent/JPS5923733B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は発泡ポリスチレン粒の着色方法に関するもので
、染料により表面を均一に着色された成形用発泡ポリス
チレン粒を得る方法を提供することを目的とするもので
ある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for coloring expanded polystyrene particles, and an object of the present invention is to provide a method for obtaining expanded polystyrene particles for molding whose surfaces are uniformly colored with a dye.

発泡ポリスチレンによる成形品の製造には、通常発泡ポ
リスチレン粒を使用するが、この発泡ポリスチレン粒に
は、発泡剤として化学発泡剤や炭化水素系ガスが含ませ
てある。
In the production of molded articles made of expanded polystyrene, expanded polystyrene particles are usually used, and the expanded polystyrene particles contain a chemical blowing agent or a hydrocarbon gas as a blowing agent.

これら発泡ポリスチレン粒を使用して着色させた発泡成
形品を製造する場合は、まず、ポリスチレンを加熱溶融
し、この中へ着色剤を練込んで着色させてから発泡ポリ
スチレン粒を混合後成形する方法があるが、これは工程
が複雑で経費がかかるうえに、発泡温度の低い発泡剤や
、ガスを含む発泡ポリスチレン粒では、ガスの漏出が多
過ぎて良好な発泡成形品は得られない。次に、発泡ポリ
スチレン粒の表面に、付着剤にて顔料や染料を付着させ
る方法もあるが、これは成形の際に、発泡ポリスチレン
粒同志の融着を粒表面の付着層が阻害して脆い成形品と
なり易い。
When producing a colored foamed molded product using these expanded polystyrene particles, first, the polystyrene is heated and melted, a coloring agent is kneaded into it to color it, and then the expanded polystyrene particles are mixed and molded. However, this process is complicated and expensive, and if a foaming agent with a low foaming temperature or foamed polystyrene particles containing gas is used, too much gas leaks out, making it impossible to obtain a good foamed molded product. Next, there is a method of attaching pigments or dyes to the surface of the expanded polystyrene particles using an adhesive, but this method prevents the adhesion layer on the particle surface from fusing the expanded polystyrene particles together during molding, resulting in brittleness. It can easily become a molded product.

本発明者らは、先に、顔料、染料等の被覆用付着剤を何
等用いることなく、しかも常温で浸漬するだけで、短時
間で均一に着色させる為には、水と有機溶剤との混合液
に染料を溶解させた染料溶液(以下単に染浴という)を
使用する方法が上述の欠点を解決するものであることを
知つて発明をなした(特許第911153号)。その後
さらに検討を続けるうち、先の発明で一旦溶解した染料
が、場合により析出、沈降して不均一層をつくり、結果
として僅かながら染着性不良部分を生じたり、濃い濃度
の染色ができにくいこともあることがわかつた。
The present inventors discovered that in order to achieve uniform coloring in a short time without using any coating adhesives such as pigments or dyes, and simply by immersing at room temperature, the inventors discovered that a mixture of water and an organic solvent was used. The inventor discovered that a method using a dye solution (hereinafter simply referred to as a dye bath) in which a dye is dissolved in a liquid solves the above-mentioned drawbacks and invented the invention (Japanese Patent No. 911153). After further investigation, we found that the dye that had been dissolved in the previous invention sometimes precipitated and settled, creating an uneven layer, resulting in slight areas with poor dyeability and difficulty in dyeing with a deep density. I found out that there are some things.

本発明者らはこの改良検討を進める中で、先の発明の水
と有機溶剤との混合液に換えて、アルコールと有機溶剤
との混合液を使用することにより、染料の析出、沈降が
起らず均i溶液となり、しかも相当に高濃度な染浴が可
能となり、ポリスチレン粒同志の溶着や、発泡性の低下
もなく、結果として先の発明をこえる効果を発揮するこ
とを見出し、本発明を完成するに至つた。すなわち、本
発明の要旨は、発泡ポリスチレン粒を着色するに当り、
アルコールおよびアルコールと相溶し、かつポリスチレ
ンを溶解する有機溶剤とよりなる混合液と、該混合液に
可溶な染料とよりなる染浴を使用することを特徴とする
発泡ポリスチレン粒の着色方法に存する。
While proceeding with this improvement study, the present inventors found that by using a mixture of alcohol and an organic solvent in place of the mixture of water and organic solvent in the previous invention, precipitation and precipitation of the dye occurred. We have discovered that it is possible to form a homogeneous solution without any problems, and to make a considerably highly concentrated dye bath possible, and there is no welding of polystyrene grains together or a decrease in foaming properties, resulting in an effect exceeding that of the previous invention, and we have developed the present invention. I was able to complete it. That is, the gist of the present invention is that when coloring expanded polystyrene particles,
A method for coloring expanded polystyrene granules, characterized by using a mixed liquid comprising alcohol and an organic solvent that is compatible with the alcohol and dissolves polystyrene, and a dye bath comprising a dye soluble in the mixed liquid. Exists.

本発明で使用するアルコールとしては通常、炭素数1〜
6、好ましくは2〜5の、更に好ましくは脂肪族系アル
コールを用いる。
The alcohol used in the present invention usually has 1 to 1 carbon atoms.
6, preferably 2 to 5, more preferably aliphatic alcohols.

具体的には、メタノール、エタノール、プロパノール、
イソプロパノール、ブタノール、イソブタノール、第3
級ブタノール、アミルアルコール、メチルセロソルブ、
エチルセロソルブ、ブチルセロソルブ、等を挙げること
ができる。又、アルコールと相溶し、スチレンを溶解す
る有機系溶剤としては、芳香族、脂肪族の炭化水素及び
これらを主成分とする混合液体、例えばトルエン、キシ
レン、ベンゼン、ガソリン、ケロシン、リグロイン、テ
トラリン、アルキルベンゼン、テレピン油、パイン油、
流動パラフイン、等や、・・ロゲン化炭化水素、例えば
、塩化メチレン、クロルベンゼン、クロルトルエン、ブ
ロムベンゼン、塩素化流動パラフイン等や、ケトン類、
例えば、メチルイソブチルケトン、メチル−n−アミル
ケトン、メチル−n−ヘキシルケトン、エチル−nブチ
ルケトン、シ一n−プロピルケトン、アセトフエノン等
や、エーテル類、例えばイソプロピルエーテル、メチル
フエニルエーテル、エチルペンシェルエーテル、フラン
等や、エステル類、例えば酢酸イソプロピル、酢酸ブチ
ル、プロピオン酸ブチル、クエン酸エステル、リシノー
ル酸エステル等の他、各種フタル酸エステルや、各種オ
レイン酸エステル、各種ステアリン酸エステル、各種ア
ジピン酸エステル、各種リン酸エステル、各種アビエチ
ン酸エステル、各種安息香酸エステル等があげられる。
Specifically, methanol, ethanol, propanol,
Isopropanol, butanol, isobutanol, tertiary
grade butanol, amyl alcohol, methyl cellosolve,
Examples include ethyl cellosolve, butyl cellosolve, and the like. In addition, examples of organic solvents that are compatible with alcohol and dissolve styrene include aromatic and aliphatic hydrocarbons and mixed liquids containing these as main components, such as toluene, xylene, benzene, gasoline, kerosene, ligroin, and tetralin. , alkylbenzene, turpentine oil, pine oil,
Liquid paraffin, etc., logenated hydrocarbons such as methylene chloride, chlorobenzene, chlorotoluene, bromobenzene, chlorinated liquid paraffin, etc., ketones,
For example, methyl isobutyl ketone, methyl-n-amyl ketone, methyl-n-hexyl ketone, ethyl-n-butyl ketone, cy-n-propyl ketone, acetophenone, etc., and ethers such as isopropyl ether, methyl phenyl ether, ethyl pen shell. In addition to ethers, furans, etc., esters such as isopropyl acetate, butyl acetate, butyl propionate, citric acid esters, ricinoleic esters, various phthalic esters, various oleic esters, various stearic esters, and various adipic acids. Examples include esters, various phosphoric acid esters, various abietic acid esters, various benzoic acid esters, and the like.

これら各種溶剤は1種または2種以上使用してもよい。These various solvents may be used alone or in combination.

本発明で使用するアルコールと有機系溶剤との混合液に
可溶な染料としては、アゾ系油溶染料、アントラキノン
系油溶染料、アミアゾ系染料、アミノアントラキノン系
染料、フタロシアニン系染料、等があり、これらは単独
あるいは二種以上混合して使用してもよい。
Dyes soluble in the mixture of alcohol and organic solvent used in the present invention include azo oil-soluble dyes, anthraquinone oil-soluble dyes, amiazo dyes, aminoanthraquinone dyes, phthalocyanine dyes, etc. , these may be used alone or in combination of two or more.

これらの着色剤を使用して発泡ポリスチレン粒を着色す
るには、通常上記の染料0.1〜10部(重量部、以下
同じ)を、アルコール100部に対し、アルコールと相
溶し、かつ、ポリスチレンを溶解する前記の如き有機系
溶剤10〜100部、好ましくは20〜60部を混合せ
る混合液に溶解させて染浴を製造する。
In order to color expanded polystyrene particles using these colorants, usually 0.1 to 10 parts (by weight, the same applies hereinafter) of the above dyes are dissolved in 100 parts of alcohol, and A dyebath is prepared by dissolving 10 to 100 parts, preferably 20 to 60 parts, of the above-mentioned organic solvent for dissolving polystyrene in a mixed solution.

得られた染浴を10〜40℃に保ち、例えば該染浴10
0部中に発泡ポリスチレン粒50〜100部を入れて5
〜30分間攪拌し、しかる後、発泡ポリスチレン粒を染
浴より取出し、風乾することにより容易に均一に着色さ
れた発泡ポリスチレン粒が得られる。
The obtained dye bath is kept at 10 to 40°C, for example, the dye bath 10
Add 50 to 100 parts of expanded polystyrene grains to 0 parts.
After stirring for ~30 minutes, the expanded polystyrene granules are taken out from the dye bath and air-dried to easily obtain uniformly colored expanded polystyrene granules.

このように本発明の方法は常温処理によるため、該処理
中発泡ポリスチレン粒が発泡するおそれは全くないのみ
ならず、発泡ポリスチレン粒の表面には顔料・染料の付
着剤等が存在しないため、成型の際、ポリスチレン粒間
の融着を阻害することなく容易にすぐれた着色成型品を
得ることができる。
As described above, since the method of the present invention involves room-temperature treatment, there is no risk of foaming of the expanded polystyrene particles during the treatment, and since there is no adhesive for pigments or dyes on the surface of the expanded polystyrene particles, molding is possible. At this time, excellent colored molded products can be easily obtained without inhibiting the fusion between polystyrene particles.

本発明の染浴として、ポワスチレン粒を溶解しない溶剤
と、溶解する溶剤との混合液を使用することが極めて重
要である。
It is extremely important to use a mixture of a solvent that does not dissolve the poistyrene grains and a solvent that does dissolve the poistyrene grains in the dyebath of the present invention.

その理論的根拠は明確ではないが、スチレン粒を溶解す
る溶剤と、溶解しない溶剤との種類と比率とが特定の条
件になつたときにのみ、スチレン粒同志を溶着させるこ
となく、スチレン粒の表面に均一、かつ、強固に、しか
も濃淡自在に染色することができることは実験の結果確
認されたものなのである。
The rationale for this is not clear, but only when the type and ratio of the solvent that dissolves the styrene grains and the solvent that does not dissolve the styrene grains meet certain conditions, the styrene grains can be dissolved without welding together. Experiments have confirmed that the surface can be dyed uniformly and strongly, and in varying shades.

もし、ポリスチレンを溶解し易い溶剤のみによる染液に
発泡ポリスチレン粒を浸漬すると、先づ、粒の表面が軟
化膨潤し、次いでポリスチレンの溶解、脱落が始まる。
If expanded polystyrene grains are immersed in a dye solution containing only a solvent that easily dissolves polystyrene, the surface of the grains will first soften and swell, and then the polystyrene will begin to dissolve and fall off.

その為、発泡ポリスチレン粒中の化学発泡剤又は、炭化
水素系ガスが露出されてしまい、発泡成形が困難となる
ばかりでなく、ポリスチレン粒同志の溶着やポリスチレ
ン粒の一部が溶解流出するなどの欠点のため実用化は不
可能である。そこで、ポリスチレンを溶解しないアルコ
ールと、ポリスチレンを溶解する有機溶剤とを特定比率
で混合した溶剤を染料溶媒として使用すると、ポリスチ
レン粒表面の溶解、脱落はおこりにくくなり、しかも、
ポリスチレンへの染料の浸透力、すなわち染着力も生ず
るので、結果として先の発明と変らない効果を得たが、
特筆すべきことは、先の発明では、染料溶媒の」部に染
料を溶解しない溶媒として水を使用したので、染料濃度
によつては染料が析出沈降することもあつたが、本発明
の染料溶媒中には、染料不溶解成分は存在してないので
、どのような染料濃度にしようとも決して染料の析出沈
降はおこらなくなり、染色ムラや濃度の点で、先の発明
よりも優れた効果を得ることができるようになつたので
ある。
As a result, the chemical blowing agent or hydrocarbon gas in the expanded polystyrene grains is exposed, which not only makes foam molding difficult, but also causes problems such as welding of the polystyrene grains to each other and a portion of the polystyrene grains dissolving and flowing out. Its shortcomings make it impossible to put it into practical use. Therefore, if a solvent that is a mixture of alcohol that does not dissolve polystyrene and an organic solvent that dissolves polystyrene in a specific ratio is used as a dye solvent, dissolution and falling off of the surface of polystyrene grains will be less likely to occur.
Since the ability of the dye to penetrate into polystyrene, that is, the ability to dye it, resulted in the same effect as the previous invention,
What should be noted is that in the previous invention, water was used as a solvent that does not dissolve the dye in the dye solvent, so depending on the dye concentration, the dye could precipitate and precipitate, but the dye of the present invention Since there are no dye-insoluble components in the solvent, no matter what the dye concentration, dye precipitation will never occur, and this invention has better effects than the previous invention in terms of dyeing unevenness and density. Now it is possible to obtain it.

本発明で染料溶媒として使用する混合溶剤として、アル
コール100部に対して、アルコールを相溶し、かつ、
ポリスチレンを溶解する有機系溶剤10〜100部、好
ましくは20〜60部を混合した溶剤を使用すればよい
As the mixed solvent used as a dye solvent in the present invention, alcohol is dissolved in 100 parts of alcohol, and
A solvent mixed with 10 to 100 parts, preferably 20 to 60 parts of an organic solvent that dissolves polystyrene may be used.

該有機系溶剤が前記割合より少な過ぎると染着効果が減
少して所望の着色がされにくく、逆に多過ぎるとポリス
チレソ粒同志の溶着や、発泡剤の放出がはじまり、成形
不良となつてしまうのである。
If the organic solvent is less than the above ratio, the dyeing effect will be reduced and it will be difficult to achieve the desired coloring, while if it is too much, the polystyrene particles will begin to weld together and the blowing agent will start to release, resulting in poor molding. It is.

次に本発明をさらに実施例により説明するが、本発明は
これらに限定されるものではない。
Next, the present invention will be further explained by examples, but the present invention is not limited thereto.

実施例 1モノアゾ系染料SudanYellOwGG
N(SOlvent.YellOw56.BASF社製
)4部をメタノール150部、テトラヒドロフラン50
部混合液に溶解させて染浴を製造する。
Example 1 Monoazo dye SudanYellOwGG
4 parts of N (Solvent.YellOw56.BASF) were mixed with 150 parts of methanol and 50 parts of tetrahydrofuran.
A dyebath is prepared by dissolving it in a mixed solution.

得られた染浴を35゜Cに保ち、これに発泡ポリスチレ
ン粒(鐘淵化学社製カネパールGM)100部を入れ1
5分間撹拌し、しかる後発泡ポリスチレン粒を染浴より
取出し風乾することにより均一に着色された発泡ポリス
チレン粒が得られた。この発泡ポリスチレン粒の着色濃
度はきわめて高く、着色粒子を1mm厚のプレス板に挟
み、150℃に調整した加熱プレスで発泡成形し、着色
濃淡を判定せる所、極めて均一なので、染色性は良好と
判定された。又、着色発泡ポリスチレン粒を白色の間に
挟み、手で強く摩擦して、白紙への色の移行を観察した
が、全く着色しないので染着性も良好という評価が得ら
れた。実施例 2 実施例1のメタノールに代えエタノールにした以外は全
て同様にして、均一に着色された発泡ポリスチレン粒を
得たが、その染着性及び染色性は極めて良好な結果が得
られた。
The obtained dyebath was maintained at 35°C, and 100 parts of expanded polystyrene grains (Kaneru GM manufactured by Kanebuchi Kagaku Co., Ltd.) were added thereto.
After stirring for 5 minutes, the expanded polystyrene particles were taken out from the dye bath and air-dried to obtain uniformly colored expanded polystyrene particles. The color density of these expanded polystyrene particles is extremely high, and the colored particles are sandwiched between 1 mm thick press plates and foam-molded using a heated press adjusted to 150°C.The color density is judged to be extremely uniform, so the dyeability is good. It was judged. In addition, colored expanded polystyrene particles were sandwiched between white sheets and rubbed strongly by hand to observe the transfer of color to the white paper. Since no color was formed at all, the dyeability was evaluated to be good. Example 2 Uniformly colored expanded polystyrene particles were obtained in the same manner as in Example 1, except that ethanol was used instead of methanol, and very good results were obtained in terms of dyeability and dyeability.

実施例 3 実施例1のテトラヒドロフランに代えトルエンにした以
外は全て同様にして、均一に着色された発泡ポリスチレ
ン粒を得たが、その染着性及び染色性は極めて良好な結
果が得られた。
Example 3 Uniformly colored expanded polystyrene particles were obtained in the same manner as in Example 1 except that toluene was used instead of tetrahydrofuran, and very good results were obtained in terms of dyeability and dyeability.

実施例 4 アンスラキノン系染料MacrOlexBlueFR(
SOlventBlve78.Bayer社製)0,5
部をメタノール150部、テトラヒドロフラン50部混
合液に溶解させて染浴を製造した以外は全て実施例1と
同様の試験を行ない、均一な淡いブルーに着色された発
泡ポリスチレン粒を得たが、その染着性及び染色性は極
めて良好な結果が得られた。
Example 4 Anthraquinone dye MacrOlexBlueFR (
SolventBlve78. Bayer) 0,5
The same test as in Example 1 was carried out except that a dye bath was prepared by dissolving 150 parts of methanol and 50 parts of tetrahydrofuran in a mixture of 150 parts of methanol and 50 parts of tetrahydrofuran. Very good results were obtained with regard to stainability and dyeability.

比較例 1実施例1のメタノールに代えて水にした以外
は全て実施例1と同様に行なつて、着色された発泡ポリ
スチレン粒を得たが、染着濃度は実施例1と比較して極
めて低く、染着度は約+であつた(染浴の残留染料濃度
より測定)比較例 2 実施例4のメタノールに代えて水にした以外は全て実施
例4と同様に行なつたが、発泡ポリスチレン粒はわずか
しか着色できず、実施例4と比較して約+程度の染着度
しか得られなかつた。
Comparative Example 1 The same procedure as in Example 1 was carried out except that water was used instead of methanol in Example 1 to obtain colored expanded polystyrene particles. Comparative Example 2 The dyeing degree was about + (measured from the residual dye concentration in the dye bath) Comparative Example 2 All procedures were carried out in the same manner as in Example 4 except that water was used instead of methanol in Example 4, but foaming The polystyrene grains could only be slightly colored, and compared to Example 4, only about + degree of dyeing was obtained.

比較例 3実施例1のテトロヒドロフランを使用せずに
メタノール200部の溶液を使用せる以外は全て実施例
1と同様に行なつて発泡ポリスチレン粒を着色したが、
濃度は極めて低く、実施例1と比較して約+程度の染着
度しか得られなかつた。
Comparative Example 3 Expanded polystyrene particles were colored in the same manner as in Example 1 except that a solution of 200 parts of methanol was used instead of the tetrahydrofuran in Example 1.
The concentration was extremely low, and compared to Example 1, only about + degree of dyeing was obtained.

比較例 4 実施例1のメタノールを使用せずに、テトロヒドロフラ
ン200部の溶液を使用せる以外は全て実施例1と同様
に行なつたが、発泡ポリスチレンの各粒子は互に融着し
てプロツク状となり着色ビーズを得ることはできなかつ
た。
Comparative Example 4 Everything was carried out in the same manner as in Example 1 except that a solution of 200 parts of tetrahydrofuran was used instead of the methanol used in Example 1, but each particle of expanded polystyrene was fused to each other. The beads became blocky and colored beads could not be obtained.

Claims (1)

【特許請求の範囲】[Claims] 1 発泡ポリスチレン粒を着色するに当り、ポリスチレ
ンを溶解しないアルコール100重量部、およびアルコ
ールと相溶し、かつ、ポリスチレンを溶解する有機系溶
剤10〜100重量部とよりなる混合液と、該混合液に
可溶な染料とよりなる染浴を使用することを特徴とする
発泡ポリスチレン粒の着色法。
1. For coloring expanded polystyrene grains, a mixed solution consisting of 100 parts by weight of alcohol that does not dissolve polystyrene and 10 to 100 parts by weight of an organic solvent that is compatible with alcohol and dissolves polystyrene; and this mixed solution. A method for coloring expanded polystyrene granules, which is characterized by using a dye bath consisting of a dye soluble in .
JP8654382A 1982-05-24 1982-05-24 Coloring method for expanded polystyrene particles Expired JPS5923733B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8654382A JPS5923733B2 (en) 1982-05-24 1982-05-24 Coloring method for expanded polystyrene particles

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8654382A JPS5923733B2 (en) 1982-05-24 1982-05-24 Coloring method for expanded polystyrene particles

Publications (2)

Publication Number Publication Date
JPS58204034A JPS58204034A (en) 1983-11-28
JPS5923733B2 true JPS5923733B2 (en) 1984-06-04

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP8654382A Expired JPS5923733B2 (en) 1982-05-24 1982-05-24 Coloring method for expanded polystyrene particles

Country Status (1)

Country Link
JP (1) JPS5923733B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59152933A (en) * 1983-02-17 1984-08-31 Kanegafuchi Chem Ind Co Ltd Colored expandable polystyrene bead
JPH0623266B2 (en) * 1988-03-25 1994-03-30 鐘淵化学工業株式会社 Method for producing colored expandable styrene resin particles
JP5635392B2 (en) * 2010-12-24 2014-12-03 積水化成品工業株式会社 Method for producing expandable polystyrene-based colored resin particles, method for producing colored resin pre-foamed particles, and method for producing colored resin foam molded article
JP5805966B2 (en) * 2011-03-22 2015-11-10 積水化成品工業株式会社 Method for producing expandable polystyrene colored resin particles

Also Published As

Publication number Publication date
JPS58204034A (en) 1983-11-28

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