JPS58204034A - Method for coloring expanded polystyrene particle - Google Patents
Method for coloring expanded polystyrene particleInfo
- Publication number
- JPS58204034A JPS58204034A JP8654382A JP8654382A JPS58204034A JP S58204034 A JPS58204034 A JP S58204034A JP 8654382 A JP8654382 A JP 8654382A JP 8654382 A JP8654382 A JP 8654382A JP S58204034 A JPS58204034 A JP S58204034A
- Authority
- JP
- Japan
- Prior art keywords
- dye
- expanded polystyrene
- alcohol
- polystyrene
- mixture
- 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.)
- Granted
Links
- 239000004794 expanded polystyrene Substances 0.000 title claims abstract description 29
- 238000000034 method Methods 0.000 title claims description 14
- 238000004040 coloring Methods 0.000 title claims description 7
- 239000002245 particle Substances 0.000 title abstract description 31
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000004793 Polystyrene Substances 0.000 claims abstract description 20
- 229920002223 polystyrene Polymers 0.000 claims abstract description 20
- 239000000203 mixture Substances 0.000 claims abstract description 14
- 239000003960 organic solvent Substances 0.000 claims description 11
- 239000008187 granular material Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 3
- 239000000975 dye Substances 0.000 abstract description 43
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract description 25
- 239000002904 solvent Substances 0.000 abstract description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract description 6
- 239000000853 adhesive Substances 0.000 abstract description 4
- 230000001070 adhesive effect Effects 0.000 abstract description 4
- 238000000465 moulding Methods 0.000 abstract description 4
- 239000011248 coating agent Substances 0.000 abstract description 2
- 238000000576 coating method Methods 0.000 abstract description 2
- 239000000987 azo dye Substances 0.000 abstract 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- -1 aliphatic alcohols Chemical class 0.000 description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- 238000004043 dyeing Methods 0.000 description 7
- 239000000243 solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000011259 mixed solution Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920006248 expandable polystyrene Polymers 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 239000004604 Blowing Agent Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical group COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Natural products OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 229940057995 liquid paraffin Drugs 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 description 1
- HFZLSTDPRQSZCQ-UHFFFAOYSA-N 1-pyrrolidin-3-ylpyrrolidine Chemical compound C1CCCN1C1CNCC1 HFZLSTDPRQSZCQ-UHFFFAOYSA-N 0.000 description 1
- ZEMPKEQAKRGZGQ-AAKVHIHISA-N 2,3-bis[[(z)-12-hydroxyoctadec-9-enoyl]oxy]propyl (z)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCCC(O)C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CC(O)CCCCCC)COC(=O)CCCCCCC\C=C/CC(O)CCCCCC ZEMPKEQAKRGZGQ-AAKVHIHISA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical class CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000002666 chemical blowing agent Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000010097 foam moulding Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical class CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 229920006327 polystyrene foam Polymers 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
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村に
は、発泡剤として化学兄泡剤や炭化水素系ガスが含ませ
である。これら発泡ポリスチレン粒を使用して着色させ
た発耐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。Expanded polystyrene particles are usually used to manufacture molded articles made of expanded polystyrene, and the expanded polystyrene particles contain a chemical foaming agent or hydrocarbon gas as a blowing agent. When producing colored foam-resistant molded products 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. There is a method, but this method 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.
次に、発泡ポリスチレン粒の表面に、付着剤にて顔料や
染料を付層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。Another method is to apply a layer of pigment or dye 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. This tends to result in brittle molded products.
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、シ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)(
!−使用する方法が上述の欠点を解決するものであるこ
とを知って発明金な1〜た(特許第911153号)。The present inventors discovered that in order to achieve uniform coloring in a short time by simply immersing at room temperature without using any coating adhesives such as pigments or dyes, a combination of water and an organic solvent was used. A dye solution (hereinafter simply referred to as a dye bath) in which a dye is dissolved in a mixed solution (
! - I was inventive after knowing that the method used would solve the above-mentioned drawbacks (Patent No. 911153).
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、沈降して不拘一層全つくり
、結果として僅かながら染着性不良部分を生じた凱濃い
#度の染色ができにくいこともあることがわかった。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
らず均一溶液となり、しかも相当に高am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
を晃出し、本発明を完成するに至った。After further investigation, we found that the dye that had been dissolved in the previous invention precipitated or precipitated in some cases, forming an unrestricted layer, and as a result, it was difficult to dye with a strong # degree, which caused slight poor dyeability. I found out that sometimes. 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. The inventors of the present invention have discovered that a uniform solution can be obtained without any problems, and a dye bath with a considerably high am. I was able to complete it.
すなわち、本発明の要旨は、発泡ポリスチレン粒を着色
するに当シ、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。That is, the gist of the present invention is to color expanded polystyrene grains by using a mixed solution consisting of alcohol and an organic solvent that is compatible with the alcohol and dissolves polystyrene, and a dye that is soluble in the mixed solution. The method of coloring expanded polystyrene particles is characterized by using a dye bath of:
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。具体的にu、メI’/−ル、エタノー
ル、プロパ/ −/l/、インプロパツール、ブタノー
ル、インブタノール、 第3級ブタノール、アル々アル
コール、メチルセロソルブ、メチルセロソルブ、ブチル
セロソルブ、等を挙げることができる。The alcohol used in the present invention usually has 1 to 1 carbon atoms.
6, preferably 2 to 5, more preferably aliphatic alcohols. Specific examples include u, mer'/-l, ethanol, propa/-/l/, impropatol, butanol, imbutanol, tertiary butanol, alcohol, methyl cellosolve, methyl cellosolve, butyl cellosolve, etc. be able to.
又、アルコールと相溶し、スチレ/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、例えバドルエン、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、テレビ/油、パイン油、流動パラフ
ィン、等や、ハロゲン化炭化水素、例えば、塩化メチレ
ン、クロルベンゼン、クロルトルエン、フロムヘンセン
、塩素化流動パラフィン等や、ケトン類、例えば、メチ
ルイソブチルケトン、メチル−〇−アミルケトン、メチ
ル−〇−へキシルケトン、エチル−〇−ブチルケトン、
シーn−フロビルケトン、アセトフェノン等や、エーテ
ル類、例えばインフロビルエーテル、メチルフェニルエ
ーテル、エチルペンジェルエーテル、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、各棟リン酸エステル、各棟アビエチン酸エステ
ル、各棟安息香酸エステル、等があげられる。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 badruene, xylene, benzene, gasoline, kerosene, ligroin, Tetralin,
Alkylbenzene, TV/oil, pine oil, liquid paraffin, etc., halogenated hydrocarbons, such as methylene chloride, chlorobenzene, chlorotoluene, fromhensen, chlorinated liquid paraffin, etc., ketones, such as methyl isobutyl ketone, methyl -〇-amyl ketone, methyl-〇-hexyl ketone, ethyl-〇-butyl ketone,
C-n-furovir ketone, acetophenone, etc., ethers such as inflovir ether, methyl phenyl ether, ethylpengel ether, furan, etc., and esters such as isopropyl acetate, butyl acetate, butyl propionate, citric acid ester, ricinol. In addition to acid esters, various phthalate esters, various oleate esters, various stearate esters, various adipate esters, various phosphate esters, various abietic acid esters, various benzoic esters, etc. can be mentioned.
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ボリスチレ/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 foamed Boristyre/granules using these colorants, usually 0.1 to 10 parts (by weight, the same shall apply hereinafter) of the above dyes are mixed with 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.
得られ友染浴を10〜40C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1発泡ポリスチレン粒を染
浴よシ取出し、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 tomo dye bath is maintained at 10 to 40C, for example, the dye bath 10
Add 50 to 100 parts of expanded polystyrene grains to 0 parts.
After stirring for ~30 minutes, one expanded polystyrene granule is taken out of 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.
を
本発明の染浴として、ポリスチレン粒曽溶解しない溶剤
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 polystyrene particles and a solvent that dissolves them as 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
件になったときにのみ、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かでさ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 it is possible to dye the surface uniformly, 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、脱落が始する。If expanded polystyrene particles are immersed in a dye solution containing only a solvent that easily dissolves polystyrene, the surface of the particles will first soften and swell, and then the polystyrene will begin to dissolve and fall off.
その為、兇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
ばか如でなく、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。As a result, the chemical blowing agent or hydrocarbon gas in the foamed polystyrene grains is exposed, which not only makes foam molding difficult, but also causes the polystyrene grains to weld together and some of the polystyrene grains to dissolve and flow out. Practical use is impossible due to these drawbacks.
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全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、染料溶媒の一部に染料を溶解しな
い溶媒として水を使用したので、染料濃度によっては染
料が析出沈降することもあったが、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ったのである。Therefore, if a solvent that is a mixture of an 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 polystyrene grain surface will be less likely to occur, and the dye will penetrate into the polystyrene. As a result, the same effect as the previous invention was obtained because the dyeing force, that is, the dyeing force, was generated. However, what is noteworthy is that in the previous invention, water was used as a solvent that did not dissolve the dye in a part of the dye solvent. Therefore, depending on the dye concentration, the dye may precipitate and precipitate, but since there are no dye-insoluble components in the dye solvent of the present invention, no matter what the dye concentration, the dye never precipitates. Sedimentation no longer occurs, and it has become possible to obtain better effects than the previous invention in terms of dyeing unevenness and density.
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 a mixed solvent used as a dye solvent in the present invention, per 100 parts of alcohol, 10 to 100 parts of an organic solvent that is compatible with alcohol and dissolves polystyrene;
Preferably, a mixture of 20 to 60 parts of the solvent may be used.
該有機系溶剤が前記割合より少な過ぎると呆着効釆が減
少して所望の着色がされに〈<、逆に多過ぎるとポリス
チレン粒同志の溶着や、発泡剤の放出かはじ筐り、成形
不良となってしまうのである。If the organic solvent is less than the above ratio, the adhesion effect will be reduced and the desired coloration will not be achieved.On the other hand, if it is too much, the polystyrene particles may be welded together, the blowing agent may be released, the casing may be molded, etc. It becomes defective.
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5udan Yet low G G
N (5olvent 。Example 1 Monoazo dye 5udan Yet low G G
N (5olvent.
Yel low 56.13 A S P社g)4部を
メタノ−A=150部、テトロヒドロフラン50部混合
液に溶解させて染浴を製造する。得られた染浴を35C
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Q M ) 100.部を入れ15分間攪拌し。A dye bath is prepared by dissolving 4 parts of Yel low 56.13 A SP g) in a mixture of 150 parts of methanol A and 50 parts of tetrahydrofuran. The obtained dye bath was heated to 35C
100. and stir for 15 minutes.
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’ill11ml厚のプレス板に挾み、1
50Cに調整した加熱プレスで発泡成形し、着色濃淡を
判定せる次、極めて均一なので、染色性は良好と判定さ
れた。Thereafter, 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 11 ml thick press plates.
It was foam-molded using a hot press adjusted to 50C, and the coloring density was judged to be extremely uniform, so the dyeability was judged to be good.
父、着色発泡ポリスチレン8を白色の間に挾み、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。I sandwiched colored polystyrene foam 8 between white papers and rubbed it strongly with my hands to observe the transfer of the color to the white paper, and as there was no coloration at all, the dyeability was rated as good.
実施例2
実施例1のメタノールに代えエタノールニジた以外は全
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 2 Uniformly colored expanded polystyrene particles were obtained in the same manner as in Example 1 except that methanol was replaced with ethanol, 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 granules 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MacroIex Blue F
几(Solve−nt Blve 78. Bayer
社製)0.5部をメタノール15゜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
び染色性は極めて艮好な結果が得られた。Example 4 Anthraquinone dye MacroIex Blue F
Solve-nt Blve 78. Bayer
The same test as in Example 1 was carried out, except that a dye bath was prepared by dissolving 0.5 parts (manufactured by MITSUMI Co., Ltd.) in a mixture of 15 parts methanol and 50 parts tetrahydrofuran. Granules were obtained, and the dyeability and dyeability of the particles were very good.
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
?lJ 1と同様に行なって、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、染着度は約乏−であった(
染浴の残留染料#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と同様に行なったが、発泡ポリスチレン粒はわずか
じか着色できず、実施例4と比較して約■程度の染着度
しか得られなかったO
比軟例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
に行なっ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1程度の染着度しか得
られなかった。Comparative Example 1 All procedures were carried out except for using water instead of methanol in Example 1. Colored expanded polystyrene particles were obtained in the same manner as in Example 1, but the dyeing concentration was extremely low compared to Example 1, and the degree of dyeing was approximately poor (
Comparative Example 2 The same procedure as in Example 4 was carried out except that water was used instead of methanol in the dye bath, but the foamed polystyrene particles could only be slightly colored, O Ratio Softness Example 3 The dyeing degree of only about ■ was obtained compared to Example 4. All the procedures were the same as Example 1 except that a solution of 200 parts of methanol was used instead of the tetrahydrofuran of Example 1. Expanded polystyrene particles were colored in the same manner, but the concentration was extremely low, and compared to Example 1, only about 1 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
に行なったが、発泡ポリスチレンの各粒子は互に融層し
てブロック状となり着色ビーズを得ることはできなかっ
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 in Example 1, but each particle of expanded polystyrene was mutually fused and blocked. As a result, colored beads could not be obtained.
Claims (1)
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lO〜100重置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. When coloring expanded polystyrene grains, a liquid mixture 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; A method for coloring expanded polystyrene granules, characterized by using a dye bath consisting of a dye soluble in a liquid.
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 true JPS58204034A (en) | 1983-11-28 |
JPS5923733B2 JPS5923733B2 (en) | 1984-06-04 |
Family
ID=13889914
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) |
Cited By (4)
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 |
US4979963A (en) * | 1988-03-25 | 1990-12-25 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Process for coloring expandable polystyrene beads |
JP2012131953A (en) * | 2010-12-24 | 2012-07-12 | Sekisui Plastics Co Ltd | Expandable polystyrene-based colored resin particle, method for producing the same, colored resin pre-expanded particle and colored resin expansion molded product |
JP2012197357A (en) * | 2011-03-22 | 2012-10-18 | Sekisui Plastics Co Ltd | Expandable polystyrene-based colored resin particle and method of manufacturing the same, colored resin preliminary foamed particle, and colored resin expansion molding body |
-
1982
- 1982-05-24 JP JP8654382A patent/JPS5923733B2/en not_active Expired
Cited By (5)
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 |
JPH0372658B2 (en) * | 1983-02-17 | 1991-11-19 | Kanegafuchi Kagaku Kogyo Kk | |
US4979963A (en) * | 1988-03-25 | 1990-12-25 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Process for coloring expandable polystyrene beads |
JP2012131953A (en) * | 2010-12-24 | 2012-07-12 | Sekisui Plastics Co Ltd | Expandable polystyrene-based colored resin particle, method for producing the same, colored resin pre-expanded particle and colored resin expansion molded product |
JP2012197357A (en) * | 2011-03-22 | 2012-10-18 | Sekisui Plastics Co Ltd | Expandable polystyrene-based colored resin particle and method of manufacturing the same, colored resin preliminary foamed particle, and colored resin expansion molding body |
Also Published As
Publication number | Publication date |
---|---|
JPS5923733B2 (en) | 1984-06-04 |
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