Composition for producing mass-dyed high-molecular organic polymeric material

专利摘要:
1403510 Isoindolinone-pigmented polymer compositions CIBA-GEIGY AG 3 Dec 1973 [4 Dec 1972] 55903/73 Headings C3P and C3R [Also in Division C4] Isoindolinone pigments and their metal complexes have the Formulae (II) and (I) in which R is an organic radical, X is 0 or S or imino, X 1 and Y 1 are H or halogen, alkyl, alkoxy, alkoxycarbonyl, alkylsulphonyl or alkyl carbamoyl of 1-6 C, or nitro, carbamoyl or arylcarbamoyl, or the radicals X 1 and Y 1 form a fused benzene ring, X 2 is H, Y is halogen and X is nitro, carbamoyl or phenyl carbamoyl, alkylcarbamoyl of 2-6 C or a group R 1 Y 2 -, wherein R 1 is H, C 1-6 alkyl, C 5-6 cycloalkyl, aralkyl or aryl, and Y 2 is O or S, m is 0 to 4, n is 0 to 4, p is 0 to 3 and the sum of m + n + p (in each ring) must be 4, while M is a polyvalent metal atom other than an alkaline earth metal atom. When milled into polyvinyl chloride, the pigment gives a yellow or reddish-yellow film. Mixed with polyethylene terephthalate granules and melt spun, the pigment dyes the filaments vivid yellow. A lacquer containing the pigment, coconut alkyd resin, melamine-formaldehyde resin, TiO 2 , and solvent gives a yellow covering on aluminium foil. With the pigment distributed in a solvent mixture containing a levelling agent and acrylic plus melamine binders, a lacquer, which may be applied to sheet metal by spraying dipping, or continuous coating, gives a yellow finish.
公开号:SU1063290A3
申请号:SU752192802
申请日:1975-11-21
公开日:1983-12-23
发明作者:Фрей Кристоф
申请人:Циба-Гейги Аг (Фирма)；
IPC主号:

专利说明:

The invention relates to dyeing and finishing production, in particular, to compositions for obtaining a high-molecular organic polymer material which is colored in oil.
The known composition G1 for the preparation of an oil-painted high-molecular organic polymer material containing a metal complex of a nitrogen-containing heterocycle of the general formula
where M is a divalent metal ion.
a nitrogen-containing heterocycle complex contains a compound of the general formula
Yii
M is cobalt, copper or nickel, R is methyl, phenyl, cyan, an ester or amide group of a carboxylic acid, or a group of the formula and a polymer selected from the group: polyethylene, polyacrylonitrile, polypropylen, flax, polyvinyl chloride, polyethylene temperate phthalate, acrylic resin , melamine resin, melamine formaldehyde resin, alkyd osmol or its mixture with melamine resin, melamine-formaldehyde resin in the following ratio of components, weight,%: Metal complex nitrogen-containing heterocycle 0,1,1,0,0, Polymer Rest of The composition in The low migration resistance of the high molecular weight organic polymer material stains. The aim of the invention is to increase the migration resistance of the color. This goal is achieved by the fact that the composition for the preparation of color. oil-containing high-molecular organic polymer material containing a metal complex of a nitrogen-containing heterocycle and a polymer selected from the group consisting of polyvini / condition, polyethylene terephthalate, acrylic resin, polyacrylonitrile polyethylene, polypropylene, alkyd resin or a mixture of melamine cream, a cream, an acrylic resin, polymethylene polyacrylonitrile, polypropylene, alkyd resin, or a melamine-styled polyethylene resin, acrylic resin, polypropylene polymer as metal X - oxygen, sulfur or imino group; hydrogen, chlorine, methyl, ethoxy, nitro, and carbamoyl, or X: and y form a benzene ring attached by condensation; Xg is hydrogen, y is chlorine, bromine, Z is a nitro or methoxy group, m 0-4, n 0-4,. p 0-h3, with m + n + p 4; in the following ratio, wt.%: Metal complex of nitrogen-containing heterocycle0, 2-10.0 Polymer Rest Example 1. 16 weight.h. 2-cyanmethyl-benzimidazole and 19 weight.h. iminophthalimide hydrochloride is heated by stirring 1a, to 130-135 in 150 weight parts of ethylene glycol monoethyl ether, then kept for 3 hours at this temperature. After cooling, the precipitate is filtered off under suction, dusted with methanol and water and dried. In vacuo with a VO-C, to obtain a yellow
Acetate
Yellow nickel
7
eight
JC VcHzCN 9
N
H
10 11
CHgCN
12
Same a
Yellow with green tint
Yellow
Also
but
Yellow with red tint
3.68 parts by weight, 2-cyanmethyl-ben-amig diazole, 4.37 parts by weight iminophthalimide hydrochloride and 1.95 parts by weight Nickel acetate is aggravated, stirring, for 15 hours to 145–150 seconds per 100 weight parts,
Continued table. one
dimethylformamide. Then it is filtered in hot form, hot-chlorobenzene, methanol and water are dried under vacuum to obtain a yellow pigment powder. CHj-CN 4-chloro-3,3-dimethoxy-isoindolinone 6-nitro-3,3-dimethoxy-the same isoindolinone 6-nitro-3,3-dimethoxy- Copper isoindolinone acetate 4,5,7-trichloro-3,3, 6- Same trimethoxy isoindoc -X
II CH2-CN Xjj /
I N Nickel Acetate Cobalt Acetate Nickel Acetate
Yellow
Acetate
The same nickel yellow with green cast Yellow Yellow with red shimmer Yellow with red shimmer Yellow with brown shimmer 5 ° (H | VcHrCONH
52
Also
Acetate
The same cobalt is 4,5,6,7-tetrachloro, 3-dimethoxy-eoindolinone Continued with. 2 r: z :::::: E: i Yellow Acetate Yellow with copper brown tint
4,5,6,7-tetrachloro-3, 3-dimethoxyisoindolines
Also
Acetate
Orange copper
same
Acetate
Yellow with
brown nickel
low tide
5-chloro-3, 3-dimethoxy-isoindolinone
Also
Yellow with
green
low tide
6-iodine-3, 3-dimethokei- Cobalt isoindolinone acetate
Yellow
Example 59 to 6.6 wt.h. 4,5,6,7-tetrachloro-3,3-dimethoxy-isoindolinone as in Example 5 is dissolved with 20 parts by weight. by volume of 1N sodium methoxide solution in 60 parts by weight methanol s. Then 3.14 wtCoCH is added. 2-Cyanmethylbenzimidazole and 1 hour stir at room temperature. After this, 2.6 parts by weight are added. Cobalt acetate with 4UnO is heated under reflux at this temperature for another 1-2 hours stirred. After addition of 5 parts by weight glacial acetic acid for another 2 hours hold with stirring at reflux temperature. Then the filter is heated in hot form, heated with hot o-dichlorobenzene, cold methanol and water, and the pigment powder is dried at approximately 100 ° C in vacuum. When rolling in PVC, a film of good strength, yellow with red cast, is obtained. The lacquer coating pigmented by this product is very weather-resistant and light-resistant.
Example 60. To 12.8 weight.h. . phthal odinitrile in 100 weight.h. ethylene glycol monoethyl ether and 20. water is added 20% by weight of 1.30% sodium hydroxide solution. The reaction takes place instantly, with the temperature rising to 38-40 ° C, then stirring for another 3 hours at approximately 40 ° C, then adding 15.7 parts by weight. 2-cyanmethylbenzimidazole is heated to about half an hour and 15 parts by weight is added. glacial acetic acid and another 1 h is maintained at this temperature. After cooling, they are filtered, washed with methanol and water and dried in vacuum at 100 ° C.
Example 61. Suitable for the manufacture of fiber, unmatted polyethylene terephthalate granules are processed for 15 minutes in a closing container together with 1% of dye 1 per

权利要求:
Claims (1)
[1]
-, (54 'COMPOSITION FOR PRODUCTION. HIGH-MOLECULAR ORGANIC POLYMERIC MATERIAL DYED IN OIL, containing a metal complex. Nitrogen-containing heterocycle and a polymer selected from the group consisting of polyvinyl chloride, polyethylene terephthylene resin, polyethylene terephthylene resin, polyethylene terephthylene resin, polyethylene terephthylene resin, polyethylene terephthylene resin or a mixture thereof with a melamine resin or a melamine-formaldehyde resin, characterized in that, in order to increase the migration resistance of the color, as a metal complex of nitrogen-containing hetero it contains a compound of the general formula where M is cobalt, copper or nickel;
R is methyl, phenyl, cyan, a carboxylic acid ester or amide group or a group of the general formula wherein x is oxygen, sulfur or an imino group;
x ₁ and y are hydrogen, chlorine, methyl, ethoxy, nitro and carba, the methyl group or and y form a benzene ring attached by condensation;
K2 hydrogen;
у - chlorine, bromine;
Z is a nitro or methoxy group, 'tn = 0-4, h = 0-4, p = 0-3, with m + p + P - 4, in the following ratio of components, wt.%:
Metal complex of nitrogen-containing heterocycle Polymer
0.2-10.0
Rest

类似技术:

---

公开号 | 公开日 | 专利标题

---

SU1063290A3|1983-12-23|Composition for producing mass-dyed high-molecular organic polymeric material

---

US4931566A|1990-06-05|Process for the preparation of pyrrolo[3,4-c]pyrroles

---

CS228540B2|1984-05-14|Method for dyeing high-molecular organic material in mass

---

US4838943A|1989-06-13|Compounds useful as pigments containing one or more 2,2,6,6-tetraalkylpiperidine groups

---

US4044036A|1977-08-23|Metal complexes of bis-azomethines from hydroxy-aldehydes and alkylene diamines

---

US4384973A|1983-05-24|Dimethine compounds of the coumarin series, a process for their preparation and their use as luminous dyestuffs

---

EP0098808B1|1986-11-26|Preparation of 1,4-diketopyrrolo-|-pyrroles

---

DE2442315A1|1975-03-13|NEW AZOMETHINE PIGMENTS AND PROCESS FOR THEIR PRODUCTION

---

US3979386A|1976-09-07|Iminoisoindoline pigments and processes for the preparation thereof

---

CH680367A5|1992-08-14|

---

US5817832A|1998-10-06|Blue diketopyrrolopyrrole pigments

---

US4065462A|1977-12-27|Iminoisoindolinone metal complex

---

US5755875A|1998-05-26|Fluorescent chromophores containing cyanimino groups

---

US3892750A|1975-07-01|New azomethine pigments and processes for their manufacture

---

US4009165A|1977-02-22|Naphtholactam dyes

---

US5378276A|1995-01-03|Diketopyrrolopyrroles containing nitroxyl groups

---

US3483213A|1969-12-09|Tetrahalogeno isoindoline pigments

---

DE2157547B2|1978-07-20|Perinon dyes, processes for their preparation and their use

---

US4052410A|1977-10-04|Iminoisoindoline pigments

---

US4116959A|1978-09-26|Isoindoline pigments

---

WO2004085542A1|2004-10-07|Heterocyclic dyes based on benzodipyrroles

---

US4042611A|1977-08-16|Water-in-soluble disazo methine compounds

---

US3926987A|1975-12-16|Dioxazine dyes

---

US4725685A|1988-02-16|Novel isoindoline compounds, their metal complexes and their use as pigments

---

US4097484A|1978-06-27|Mixed complexes of methine dyes

同族专利:

---

公开号 | 公开日

---

NL7316597A|1974-06-06|

---

DE2359791C3|1979-07-12|

---

AR200749A1|1974-12-13|

---

NL176862C|1985-06-17|

---

CH580678A5|1976-10-15|

---

JPS5544783B2|1980-11-14|

---

BE808134A|1974-06-04|

---

FR2208942A1|1974-06-28|

---

AU6244573A|1975-05-15|

---

DK143808C|1982-03-29|

---

CS176258B2|1977-06-30|

---

DE2359791B2|1978-10-12|

---

FR2208942B1|1976-06-25|

---

GB1403510A|1975-08-28|

---

US3897439A|1975-07-29|

---

DK143808B|1981-10-12|

---

AU476693B2|1976-09-30|

---

NL176862B|1985-01-16|

---

JPS4987732A|1974-08-22|

---

BR7309471D0|1974-09-24|

---

CA996562A|1976-09-07|

---

DE2359791A1|1974-06-06|

引用文献:

---

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

---

---

US3256291A|1965-03-08|1966-06-14|Du Pont|Neutral and ionic chelates of 1-pyrazoledithiocarboxylic acids with divalent metals of atomic number 24-30|

---

US3481945A|1966-12-09|1969-12-02|Moleculon Corp|Tetrabenzimidazole|

---

US3678007A|1971-08-23|1972-07-18|Ppg Industries Inc|Metal salt complexes of imidazolium salts as curing agents for one part epoxy resins|US3919235A|1972-11-20|1975-11-11|Sterling Drug Inc|Polycyclic iminoisoindoline chelates|

---

US4002635A|1972-12-04|1977-01-11|Ciba-Geigy Corporation|Isoindolinone compounds useful in preparing heavy metal containing pigments|

---

US4111947A|1974-02-06|1978-09-05|Ciba-Geigy Corporation|Novel metal complexes of azomethines and process for their manufacture|

---

CH594721A5|1974-09-05|1978-01-31|Ciba Geigy Ag|

---

CH606335A5|1974-10-17|1978-10-31|Ciba Geigy Ag|

---

CH606282A5|1974-10-17|1978-10-31|Ciba Geigy Ag|

---

DE2848622A1|1978-11-09|1980-05-22|Bayer Ag|ACID MONOMETHINE METAL COMPLEX DYES|

---

CH644145A5|1979-05-02|1984-07-13|Sandoz Ag|Metal complexes of oximinoverbindungen and their use as pigments.|

---

EP0023889B1|1979-08-03|1983-03-09|Ciba-Geigy Ag|Iminoisoindolinone metal complexes, process for their manufacture, method for pigmenting an organic high-molecular material and high-molecular organic material containing such a metal complex|

---

US4515955A|1982-03-08|1985-05-07|Minnesota Mining And Manufacturing Company|Isoindoline cationic dyes|

---

DE3443465A1|1984-11-29|1986-05-28|Basf Ag, 6700 Ludwigshafen|NEW ISOINDOLINE COMPOUNDS, THEIR METAL COMPLEXES AND THEIR USE|

---

DE3508553A1|1985-03-11|1986-09-11|Hüls AG, 4370 Marl|METHOD AND DEVICE FOR CATALYTICALLY CONVERTING GASES|

---

TW217426B|1992-01-08|1993-12-11|Mekku Kk|

---

US5571359A|1992-01-24|1996-11-05|Revlon Consumer Products Corporation|Radiation curable pigmented compositions|

---

US5667856A|1992-01-24|1997-09-16|Revlon Consumer Products Corporation|Radiation curable pigmented compositions and decorated substrates|

---

US6136382A|1997-12-29|2000-10-24|Deco Patents, Inc.|Method and compositions for decorating vitreous articles with radiation curable inks having improved adhesion and durability|

法律状态:

优先权:

---

申请号 | 申请日 | 专利标题

---

CH1762572A|CH580678A5|1972-12-04|1972-12-04|

---