JPS58171452A - Colorant for thermoplastic resin - Google Patents

Colorant for thermoplastic resin

Info

Publication number
JPS58171452A
JPS58171452A JP4746182A JP4746182A JPS58171452A JP S58171452 A JPS58171452 A JP S58171452A JP 4746182 A JP4746182 A JP 4746182A JP 4746182 A JP4746182 A JP 4746182A JP S58171452 A JPS58171452 A JP S58171452A
Authority
JP
Japan
Prior art keywords
hydroxystearic acid
colorant
resins
pigment
parts
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
Application number
JP4746182A
Other languages
Japanese (ja)
Other versions
JPS6058264B2 (en
Inventor
Takaaki Osanai
長内 隆明
Toshio Iizuka
飯塚 利夫
Tomiji Shichizawa
七沢 富治
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.)
Dainichiseika Color and Chemicals Mfg Co Ltd
Original Assignee
Dainichiseika Color and Chemicals 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 Dainichiseika Color and Chemicals Mfg Co Ltd filed Critical Dainichiseika Color and Chemicals Mfg Co Ltd
Priority to JP4746182A priority Critical patent/JPS6058264B2/en
Publication of JPS58171452A publication Critical patent/JPS58171452A/en
Publication of JPS6058264B2 publication Critical patent/JPS6058264B2/en
Expired legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

PURPOSE:To prepare the titled colorant having excellent dispersibility in resins, and giving a colored product free from mottling, by adding an amide wax of hydroxystearic acid as a dispersing agent to a dye or pigment. CONSTITUTION:The objective colorant is prepared, e.g. by adding preferably 20-200pts.wt. of an amide wax of hydroxystearic acid (e.g., hydroxystearic acid monoamide, hydroxystearic acid methylenebisamide, etc.) as a dispersing agent to 100pts.wt. of a dye or pigment.

Description

【発明の詳細な説明】 本発明は熱可塑性樹脂用着色剤に係夛、%に染顔料の分
散助剤としてとドロキシステアリン酸のアミドワックス
を用い、優れた粒子分散性を有する熱可塑性樹脂用着色
剤を提出するものである。従来、熱可塑性樹脂用の着色
剤として使用する染顔料の分散助剤としてステアリン酸
の金属塩、例えばステアリン酸カルシウム、ステアリン
酸マグネシウムおよびステアリン酸亜鉛郷の新調ステア
リン酸の金属石けんが使用されていることは公知である
DETAILED DESCRIPTION OF THE INVENTION The present invention is applied to colorants for thermoplastic resins, and uses amide wax of droxystearic acid as a dispersion aid for dyes and pigments to produce thermoplastic resins with excellent particle dispersibility. colorants for use in the market. Conventionally, metal salts of stearic acid, such as calcium stearate, magnesium stearate, and zinc stearate's newly prepared metal soaps of stearic acid, have been used as dispersion aids for dyes and pigments used as colorants for thermoplastic resins. is publicly known.

ところが、前記した金属石けんは熱可塑性樹脂との相溶
性に限界があるため、樹脂選択性があシ、相溶性の悪い
樹脂に対しては大量に使用すると成形加工時のスリップ
、樹脂からの分離、剥離や樹脂の棲械的強度を低下せし
め菜堝合があ抄、も満足できるもので力かった。
However, the above-mentioned metal soap has limited compatibility with thermoplastic resins, so resin selectivity is poor, and when used in large quantities with resins with poor compatibility, slipping during molding and separation from the resin may occur. However, the effects of peeling and reducing the mechanical strength of the resin were also satisfactory and effective.

更にまたポリオレフィンワックスの場合はポリスチレン
・ポリプロピレン郷のポリオレフィン樹脂おヨヒエチレ
ンー酢酸ビニル共重合樹脂、ブチルゴム勢樹脂に対して
は十分相溶するものの、ポリスチレン、Al1などのス
チレン系樹脂およびポリメチルメタクリレ−ト樹脂、ポ
リカーボネート樹脂に大量に用いた場合、白濁、分離、
剥離や物性低下を起こし、染顔料を着色剤化した場合の
色むら性能も満足できるものではなく5使用に適した樹
脂の幹囲が狭いという欠陥があった。
Furthermore, in the case of polyolefin wax, although it is sufficiently compatible with polyolefin resins such as polystyrene and polypropylene, ethylene-vinyl acetate copolymer resins, and butyl rubber resins, it is compatible with styrene resins such as polystyrene and Al1, and polymethyl methacrylate. When used in large quantities for resins and polycarbonate resins, cloudiness, separation,
Peeling and deterioration of physical properties occurred, and when dyes and pigments were used as colorants, the color unevenness performance was also unsatisfactory, and there was a defect that the trunk circumference of the resin suitable for use in 5 was narrow.

そこで本発明者は前記せる従来の着色剤の粒子分散不良
あるいは拡散性不良に基因する色むら発生を改善すべく
、顔料の分散助剤について種々研究を進めた結果、ヒド
ロキシステアリン酸のアミドワックスが、顔料の粒子分
散性改善に極めて有効であり、かつ広閣囲の樹脂に使用
することができることを知見し、本発明に到達した。
Therefore, in order to improve the color unevenness caused by poor particle dispersion or poor diffusivity of the conventional colorants mentioned above, the present inventor conducted various research on pigment dispersion aids, and found that amide wax of hydroxystearic acid The present invention was achieved based on the findings that the method is extremely effective in improving the particle dispersibility of pigments and can be used in Kokakuho resins.

即ち本発明は染顔料にヒドロキシステアリン酸のアミド
ワックスを添加したことを特徴とする熱可塑性樹脂用着
色剤に関するものである。
That is, the present invention relates to a coloring agent for thermoplastic resins characterized by adding hydroxystearic acid amide wax to dyes and pigments.

本発明における熱可塑性樹脂とは例えば、ポリエチレン
、ポリプロピレン、ポリブテン−1、ポリスチレン、ポ
リ塩化ビニル、ポリカーボネート、ポリメチルメタクリ
レート、AlB、ム8およびZVム等の合成樹脂が挙げ
られる。
Examples of the thermoplastic resin in the present invention include synthetic resins such as polyethylene, polypropylene, polybutene-1, polystyrene, polyvinyl chloride, polycarbonate, polymethyl methacrylate, AlB, Mu8, and ZVmu.

本発明において着色剤の主成分として使用される染顔料
は当該技術分野で従来から使用されている染顔料であり
、具体的には例えばアゾ系、フタロシアニン系、キナク
リドン系、イソインドリノン系、チオインジゴ系、ペリ
レン系およびペリノン系郷の有機染顔料、酸化チタン、
コバルトブルー、ベンガラおよび黄鉛等の無機顔料およ
びカーボンブラック等が挙けられる。
The dyes and pigments used as the main components of the colorant in the present invention are dyes and pigments conventionally used in the technical field, and specifically include azo, phthalocyanine, quinacridone, isoindolinone, and thioindigo dyes. organic dyes and pigments, titanium oxide,
Examples include inorganic pigments such as cobalt blue, red iron and yellow lead, and carbon black.

また本発明に使用されるヒドロキシステアリン酸の72
ドワツクスとしては例えばヒドロキシステアリン酸モノ
アミド、ヒドロキシステアリン酸ビスアミド、ヒドロキ
システアリン酸メチレンビスアミドおよびヒドロキシス
テアリン酸エチレンビスアミド等が挙げられる。
In addition, 72 of the hydroxystearic acid used in the present invention
Examples of the doxes include hydroxystearic acid monoamide, hydroxystearic acid bisamide, hydroxystearic acid methylene bisamide, and hydroxystearic acid ethylene bisamide.

前記ヒドロキシステアリン酸のアミドワックスは1種な
いし2種以上添加使用される。
One or more of the hydroxystearic acid amide waxes may be used in combination.

前記染腰料に対するヒドロキシステアリン酸のアミドワ
ックスの添加量は染顔料100重景量比対し、ヒドロキ
システアリン酸のアミドワックスを5〜900重量部、
好ましくは20−400重量部である。
The amount of hydroxystearic acid amide wax added to the dye/pigment is 5 to 900 parts by weight per 100 parts by weight of the dye/pigment.
Preferably it is 20-400 parts by weight.

なお、本発明においてはとドロキシステアリン酸のアミ
ドワックスに従来公知の脂肪酸の金属石けん、ポリオレ
フィンワックスなどの分散剤を併用して使用することも
できる。
In addition, in the present invention, a dispersant such as a conventionally known fatty acid metal soap or polyolefin wax may be used in combination with the amide wax of drooxystearic acid.

また、ヒドロキシステプリン酸のアミドワックスと染顔
料を熱可塑性樹脂に高濃度に混和してマスターバッチと
し、このマスターバッチをナチュラルの熱可塑性樹脂と
混和して使用することもできる。
It is also possible to mix hydroxystepric acid amide wax and dye and pigment in a thermoplastic resin at a high concentration to form a masterbatch, and use this masterbatch by mixing it with a natural thermoplastic resin.

以下、実施例により本発明を具体的に設明する。Hereinafter, the present invention will be concretely established through Examples.

なお、実施例、比較例中、部とあるのはsi部を指すも
のである。
In addition, in Examples and Comparative Examples, part refers to si part.

実施例1゜ ルチル型醗化チタン40部、銅フタロシアニンブルー2
0部およびヒドロキシステアリン酸ビスア電ド40部を
160〜170℃に加熱し九双腕型ニーダ−に投入し、
回転数6Or−で10分間混線後ニーダーを水冷しなが
ら混線物をブロック状で皐り出す。次いで混線物を十分
冷却し、粗砕した後、マイクロサンプルミル(株式会社
細川鉄工所製粉砕機)で粉砕し、粒度16〜60メツシ
ユの顆粒状着色剤1を得た。
Example 1 40 parts of rutile titanium fluoride, 2 parts of copper phthalocyanine blue
0 parts and 40 parts of hydroxystearic acid bisacide were heated to 160 to 170°C and charged into a nine double-arm kneader,
After mixing for 10 minutes at a rotational speed of 6 Or-, the mixed material is shaken out in the form of blocks while cooling the kneader with water. Next, the mixed wire material was sufficiently cooled, crushed, and then crushed in a microsample mill (pulverizer manufactured by Hosokawa Iron Works Co., Ltd.) to obtain granular colorant 1 having a particle size of 16 to 60 mesh.

次いで、第1表に示した通り各種の熱可塑性樹脂との組
合せで前記の顆粒状着色剤を配合し、7オンスインライ
ンスクリユ一射出成形機(シリンダ一温度230℃、ス
クリュー回転数7 Q rpa+背圧10に/i)にて
、ダイレクトゲートを有する金型を用い、縦200wg
1I、横150鶴、厚さ:3mの各種熱可塑性樹脂によ
る着色成形板を得た。
Next, the above-mentioned granular colorant was blended with various thermoplastic resins as shown in Table 1, and a 7-ounce in-line screw injection molding machine (cylinder temperature 230°C, screw rotation speed 7 Q rpa+ At a back pressure of 10/i), using a mold with a direct gate, vertically 200 wg
Colored molded plates made of various thermoplastic resins were obtained, measuring 1I, 150mm wide, and 3m thick.

この各着色成形板のゲート部及びウェルド部から小片を
切υ取り、熱プレスによシ、縦、横各々100mm厚さ
約0.5fiのフィルムを作成して、フィルムの表面及
び透過の色むら状態を目視にて観察した結果第1表に示
した通り、いずれの熱可塑性樹脂フィルムにおいても着
色剤の混和不足による合むらはVめられず、極めて均一
な着色状態を呈していた。
A small piece was cut from the gate part and weld part of each colored molded plate, and it was heat pressed to make a film of 100 mm length and width and about 0.5 fi thickness, and the color unevenness of the surface and transmission of the film was made. Visual observation of the condition showed that as shown in Table 1, none of the thermoplastic resin films exhibited any unevenness due to insufficient mixing of the colorant, and an extremely uniform colored condition was observed.

又各着色成形飯から小片を切り取り、熱プレスにより厚
さ約・50pのフィルムを作成し、倍率150倍の光学
顕微鏡で粗大粒子を観察した結果第1Fに示した通り、
1視野中に20p以上の凝集した粒子F1.1個も認め
られず、極めてすぐれた粒子分散性を呈していた。
In addition, a small piece was cut from each colored molded rice, a film with a thickness of about 50p was created by heat pressing, and the coarse particles were observed using an optical microscope with a magnification of 150 times. As shown in the 1st floor,
Not even 1.1 aggregated particles F of 20p or more were observed in one field of view, indicating extremely excellent particle dispersibility.

第  1  表 比較例1 ルf ルアfJ、fl 化チタン40部、鐸フタロシア
ニンブルー20部及び低分子量ポリエチレンワックス4
0部を実施例1と同様にして粒度16〜6oメツシユの
顆粒状着色剤を得た。
Table 1 Comparative Example 1 Lua fJ, fl 40 parts of titanium oxide, 20 parts of Taku Phthalocyanine Blue and 4 parts of low molecular weight polyethylene wax
A granular coloring agent having a particle size of 16 to 6 o mesh was obtained by adding 0 part in the same manner as in Example 1.

次いで第2表に示した通り、実施例1と同様の方法で各
種熱可塑性樹脂に対する前記顆粒状着色剤の色むら及び
粒子分散性を観察した。
Next, as shown in Table 2, the color unevenness and particle dispersibility of the granular colorant in various thermoplastic resins were observed in the same manner as in Example 1.

その結果第2表に示した通シ高密度ポリエチレンにおい
ては良好な性能を呈したものの、ポリプロピレン、ポリ
スチレンおよびムB8については満足できる性能が得ら
れず樹脂汎用性にとぼしがった。
As a result, although high-density polyethylene shown in Table 2 exhibited good performance, satisfactory performance was not obtained for polypropylene, polystyrene, and Mu-B8, and the resin's versatility was compromised.

第  2  表 ペリレン系顔料(商品名;PvファーストレッドB)S
ell、!:ヒドロキシステアリン酸エチレンビスアミ
ド50を160〜170℃に加熱した双腕型ニーダ−に
投入し60 rpmで1o分間混紳後、ニーダ−を水冷
しながら混紗物をブロック状で取9出し、直ちに双軸造
粒機(商品名;ベレッター不二パウダル社製品)に供給
して加熱造粒を行ない、直径約1龍長さ約3tllの顆
粒状着色剤を得た。
Table 2 Perylene pigment (trade name: Pv Fast Red B) S
ell,! : Hydroxystearic acid ethylene bisamide 50 was put into a double-arm kneader heated to 160 to 170°C, mixed for 10 minutes at 60 rpm, and while the kneader was cooled with water, the mixed gauze was taken out in the form of a block and immediately taken out. The mixture was supplied to a twin-screw granulator (product name: Beretter Fuji Paudal Co., Ltd.) for heating and granulation to obtain a granular colorant having a diameter of about 1 liter and a length of about 3 tll.

次いで第3表に示した通り、各種の熱可塑性樹脂との組
合せで前記の顆粒状着色剤を配合し、7オンスインライ
ンスクリユ一射出成形機(シリンダ一温度230〜28
0℃、スクリュー回転数70 vpm背圧10し/−)
にて、ダイレクトゲートを有する金型を用い、縦20G
龍、横L 50 wII%厚さ3瓢の各種熱可塑性樹脂
による着色成形板を得た。
Next, as shown in Table 3, the above granular colorant was compounded in combination with various thermoplastic resins, and a 7-ounce in-line screw injection molding machine (cylinder temperature 230-28
0°C, screw rotation speed 70 vpm back pressure 10/-)
Using a mold with a direct gate, vertical 20G
Colored molded plates made of various thermoplastic resins having a length of 50 wII% and a thickness of 3 gourd were obtained.

この各着色成形板のゲート部及びウェルド部から小片を
切り取り熱プレスにより、縦、横各々100wx厚さ約
0.5籠のフィルムを作成して、フィルムの表面及び透
過の色むら状態を目視にて観察した結果第3表に示した
通り、いずれの熱可塑性樹脂フィルムにおいて亀、着色
剤の混和不足による色むらは認められず極めて均一な着
色状態を呈していた。
A small piece was cut from the gate and weld part of each colored molded plate, and a film of 100w x 0.5cm thick was created by heat pressing, and the color unevenness on the surface and transmission of the film was visually observed. As shown in Table 3, none of the thermoplastic resin films exhibited color unevenness due to lack of mixing of the coloring agent and exhibited an extremely uniform colored state.

又各着色成形板から小片を切り取り、熱プレスにより厚
さ約50声のフィルムを作成し、倍率150倍の光学顕
微骨て粗大粒子を観察した結果第3表に示した通り、1
視野中に20部以上の凝集した粒子は1個も認められず
、極めてすぐれた粒子分散性を呈していた。
In addition, a small piece was cut from each colored molded plate, a film with a thickness of approximately 50 mm was made by heat pressing, and the coarse particles were observed under an optical microscope at a magnification of 150 times. As shown in Table 3,
Not a single aggregated particle of 20 parts or more was observed in the visual field, indicating extremely excellent particle dispersibility.

第  3  表 比較例2 ペリレン系顔料(商品名;Pvファストレッドlヘキス
ト社製品)50部とステアリン酸エチレンビスアミド5
0部を実施例2と同様にして直径約1fi、長さ約31
111の顆粒状着色剤を得た。
Table 3 Comparative Example 2 50 parts of perylene pigment (trade name: Pv Fast Red product from Hoechst) and 5 parts of ethylene bisamide stearate
Part 0 was prepared in the same manner as in Example 2, with a diameter of about 1fi and a length of about 31mm.
111 granular colorants were obtained.

次いで第4表に示した通り、実#倒2と同様の方法で各
種熱可塑性樹脂に対する前記顆粒状着色剤の色むら及び
粒子分散性を観察した。
Next, as shown in Table 4, the color unevenness and particle dispersibility of the granular colorant in various thermoplastic resins were observed in the same manner as Example 2.

その結果第4表に示した通り、ポリプロピレンにおいて
はやや良好な性能を呈したもののAB8樹脂、ポリカー
ボネート樹脂については満足すべき性能が得られず樹脂
汎用性にとぼしかった。
As shown in Table 4, although polypropylene exhibited somewhat good performance, AB8 resin and polycarbonate resin did not provide satisfactory performance, resulting in poor resin versatility.

第 4 表 特許出願人 大日精化工業株式会社Table 4 Patent applicant: Dainichiseika Industrial Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 染顔料にヒドロキシステアリン酸のアミドワックスを添
加したことを特徴とする熱可塑性樹脂用着色剤。
A coloring agent for thermoplastic resins characterized by adding hydroxystearic acid amide wax to dyes and pigments.
JP4746182A 1982-03-26 1982-03-26 Colorant for thermoplastic resin Expired JPS6058264B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4746182A JPS6058264B2 (en) 1982-03-26 1982-03-26 Colorant for thermoplastic resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4746182A JPS6058264B2 (en) 1982-03-26 1982-03-26 Colorant for thermoplastic resin

Publications (2)

Publication Number Publication Date
JPS58171452A true JPS58171452A (en) 1983-10-08
JPS6058264B2 JPS6058264B2 (en) 1985-12-19

Family

ID=12775791

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4746182A Expired JPS6058264B2 (en) 1982-03-26 1982-03-26 Colorant for thermoplastic resin

Country Status (1)

Country Link
JP (1) JPS6058264B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61106660A (en) * 1984-10-30 1986-05-24 Dainippon Ink & Chem Inc Colored polycarbonate composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61106660A (en) * 1984-10-30 1986-05-24 Dainippon Ink & Chem Inc Colored polycarbonate composition
JPH0123497B2 (en) * 1984-10-30 1989-05-02 Dainippon Ink & Chemicals

Also Published As

Publication number Publication date
JPS6058264B2 (en) 1985-12-19

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