Light resistant, mono azo organic yellow pigment and method for preparing the same
A technology of yellow monoazo and organic pigments, which is applied in the preparation of light-resistant oxidation yellow monoazo organic pigments, and in the field of light-resistant oxidation yellow monoazo organic pigments, which can solve the comprehensive performance of unusable, light-resistant, heat-resistant, and migration-resistant Bad question
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
specific Embodiment approach 1
[0014] Synthesis of photofast oxidation yellow monoazo organic pigment A:
[0015] (1) 4-(4-aminobenzoate group)-2,2,6,6-tetramethylpiperidine diazotization:
[0016] Dissolve 0.01 mol of 4-4-aminobenzoate-2,2,6,6-tetramethylpiperidine in 50 ml of water and 3.5 ml of 30% hydrochloric acid. Cool to 0°C in an ice-water bath. Cool 2.5ml of sodium nitrite solution with a concentration of 4mol / L to 0°C in advance with an ice bath, and quickly add it to the reaction solution under stirring, keep the temperature at 0-5°C, and react for 1-2 hours. During the reaction, the solution was slightly blue to Congo red test paper, and slightly blue to starch potassium iodide test paper. The reaction formula is as follows:
[0017]
[0018] After the reaction, the diazonium solution is clear and transparent, and urea is added to decompose the excess sodium nitrite until the reaction solution does not change color on the starch potassium iodide test paper, and the diazonium salt solution ...
specific Embodiment approach 2
[0024] Synthesis of photofast oxidation yellow monoazo organic pigment B:
[0025] (1) Diazotization of 4-(4-aminobenzoate)-2,2,6,6-tetramethylpiperidine: same as in Embodiment 1.
[0026] (2) Synthesis of light-resistant oxidation yellow azo organic pigment:
[0027] Add 200ml of water and 0.01mole o-chloroacetoacetanilide in a 500ml beaker, adjust the pH value to 8.5-9.0 with 30% sodium hydroxide solution and stir to completely dissolve the o-chloroacetoacetanilide, filter to remove inorganic impurities, and cool to Below 5°C, uniformly add the diazonium salt solution prepared above into the reaction solution within 10-15min, adjust the pH value to 8.0-8.5 after adding, keep the temperature at 5-10°C for full reaction, and use β- The naphthol permeation ring method was used to detect the reaction end point until the diazonium salt disappeared completely, and the reaction ended. The reaction formula is as follows:
[0028]
[0029] (3) Pigmentation:
[0030] Add an app...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 