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Environment-friendly preparation method of phthalocyanine green

A phthalocyanine green, environmentally friendly technology, applied in chemical instruments and methods, porphine/acrphine, azo dyes, etc., can solve the problems of bright color, high yield, high processing cost, coarse pigment particles, etc. Improved operating environment, reduced processing costs, and enhanced tinting strength

Inactive Publication Date: 2018-05-29
滨海康益医药化工有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The pigment particles of this process are coarse and the processing performance is slightly poor, but the color is bright and the yield is slightly higher
In addition, this process produces a large amount of acidic solution containing aluminum salts and sodium salts, which is difficult to handle and requires high processing costs

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] (1) Add 2,150 kg of aluminum trichloride and 570 kg of sodium chloride into the reaction kettle. When the temperature rises to 145°C, the materials in the kettle begin to melt, and slowly start stirring. After the materials are completely melted, stop heating, and then add 495 kg of copper phthalocyanine and 60 kg of copper chloride;

[0035] (2) After adding copper phthalocyanine and copper chloride, restart the heating to 165°C, keep warm and let chlorine gas react for 18 hours, until no hydrogen chloride is produced in the tail gas detection, stop stirring and stop chlorine flow;

[0036] (3) Put 100kg of the reactants obtained in step (2) into the dilution tank, and start stirring at the same time until the temperature of the material in the dilution tank drops to 70°C, then add the material to a filter press and wash it with water until the washing liquid is neutral. Filtrate A is acidic water containing aluminum salts, and filter cake M is crude phthalocyanine gre...

Embodiment 2

[0041] (1) Add 1710 kg of aluminum trichloride and 570 kg of sodium chloride into the reaction kettle. When the temperature rises to 150 ° C, the materials in the kettle begin to melt, and slowly start stirring. After the materials are completely melted, stop heating, and then add 513 kg of copper phthalocyanine and 57 kg of copper chloride;

[0042] (2) After adding copper phthalocyanine and copper chloride, turn on the heating again to 170°C, keep warm and pass chlorine gas to react for 14 hours, until no hydrogen chloride is produced in the tail gas detection, stop stirring and stop chlorine flow;

[0043] (3) Put 100kg of the reactants obtained in step (2) into the dilution tank, and start stirring at the same time until the temperature of the material in the dilution tank drops to 70°C, then add the material to a filter press and wash it with water until the washing liquid is neutral. Filtrate A is acidic water containing aluminum salts, and filter cake M is crude phthalo...

Embodiment 3

[0048] (1) Add 2,850 kilograms of aluminum trichloride and 456 kilograms of sodium chloride to the reaction kettle. When the temperature rises to 155°C, the materials in the kettle begin to melt, and slowly start stirring. After the materials are completely melted, stop heating, and then add 495 kg of copper phthalocyanine and 86 kg of copper chloride;

[0049] (2) After adding copper phthalocyanine and copper chloride, restart the heating to 168°C, keep warm and let chlorine gas react for 16 hours, until no hydrogen chloride is produced in the tail gas detection, stop stirring and stop chlorine flow;

[0050] (3) Put 100kg of the reactants obtained in step (2) into the dilution tank, and start stirring at the same time until the temperature of the material in the dilution tank drops to 70°C, then add the material to a filter press and wash it with water until the washing liquid is neutral. Filtrate A is acidic water containing aluminum salts, and filter cake M is crude phthal...

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Abstract

The invention provides an environment-friendly preparation method of phthalocyanine green. The preparation method comprises the following steps: (1) adding alchlor and sodium chloride in a reaction kettle, raising the temperature to 145-155 DEGC, stopping heating after the materials are fully melt, sequentially adding copper phthalocyanine and copper chloride; (2) starting heating again to 165-170DEG C after finishing adding the copper phthalocyanine and the copper chloride, preserving the heat, introducing chlorine, carrying out a reaction for 14-18 hours; (3) putting a reaction liquid obtained in the step (2) into a dilution tank while the reaction liquid is hot, stirring, cooling, washing with water until a washing solution is neutral, pulping again, then adding an emulsion, washing with water again, filtering, pulping, adding dichlorobenzene to ball, and then processing to obtain a phthalocyanine green product. By adopting the preparation method, the high-quality phthalocyanine green having the advantages of fine and small particle, uniform particle size distribution, good colored light, and strong tinting strength is prepared.

Description

technical field [0001] The invention belongs to the technical field of pigment preparation, and in particular relates to an environment-friendly preparation method of phthalocyanine green. Background technique [0002] Phthalocyanine green is a perchlorinated copper phthalocyanine, with an average of 14 to 15 chlorine atoms per molecule, and its color is blue and green. Phthalocyanine green has good various application properties, for example, its light resistance, heat resistance, weather resistance and solvent resistance are quite excellent. Although green pigments can be obtained by mixing blue pigments and yellow pigments properly, the green pigments obtained by this kind of color matching cannot be compared with the pigment phthalocyanine green in terms of shade and application performance. Yellow pigments are more or less toxic, so the pigments obtained by combining blue and yellow pigments cannot be used for coloring food packaging materials. [0003] There are two ...

Claims

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Application Information

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IPC IPC(8): C09B47/10C07D487/22
CPCC07D487/22C09B47/10
Inventor 王庆刚
Owner 滨海康益医药化工有限公司