Preparation method for C.I.112 pigment red FGR
A pigment red and chromophore technology, which is applied in the preparation field of C.I. Pigment Red 112, can solve the problems of poor hydrophilic application performance of pigments, environmental pollution, low reaction conversion rate, etc., and achieves inhibition of re-aggregation, enhancement of hydrophilicity, The effect of increased utilization
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0024] Embodiment 1: the preparation method of a kind of C.I. pigment red 112 of this example, its steps are:
[0025] a. Preparation of diazo solution: Add 8 parts by weight of fatty alcohol polyoxyethylene ether to 1000 parts by weight of water to make a mixed solution, and pulp 100 parts by weight of 2.4.5-trichloroaniline into 245 mesh fineness through colloid mill After adding in the mixed solution, then the concentration of 180 parts by weight is that 31% hydrochloric acid, 15 parts by weight of octadecyl dimethyl hydroxyethyl quaternary ammonium nitrate are added in the mixed solution, beating for 1.5 hours, with The concentration of 115 weight parts is the diazotization of 30% sodium nitrite solution, makes diazonium liquid;
[0026] b. Preparation of naphthol AS-D alkaline solution: Add 135 parts by weight of NaOH with a concentration of 30% to 1000 parts by weight of water, heat up to 90°C, add 10 parts by weight of rosin resin and keep it for 0.08 hours, add 145 p...
Embodiment 2
[0029] Embodiment 2: the preparation method of a kind of C.I. pigment red 112 of this example, its steps are:
[0030] a. Preparation of diazo solution: Add 6 parts by weight of fatty alcohol polyoxyethylene ether to 1000 parts by weight of water to make a mixed solution, and pulp 99 parts by weight of 2.4.5-trichloroaniline into 240 mesh fineness through colloid mill After adding in the mixed solution, then the concentration of 175 parts by weight is that 30% hydrochloric acid, 13 parts by weight of octadecyl dimethyl hydroxyethyl quaternary ammonium nitrate are added in the mixed solution, beating for 1.5 hours, with The concentration of 113 weight parts is the diazotization of 29% sodium nitrite solution, makes diazonium liquid;
[0031] b. Preparation of naphthol AS-D alkaline solution: Add 130 parts by weight of NaOH with a concentration of 29% in 1000 parts by weight of water, heat up to 88°C, add 8 parts by weight of rosin resin and keep it for 0.08 hours, add 143 par...
Embodiment 3
[0034] Embodiment 3: the preparation method of a kind of C.I. pigment red 112 of this example, its steps are:
[0035] a. Preparation of diazo solution: Add 7 parts by weight of fatty alcohol polyoxyethylene ether to 1000 parts by weight of water to make a mixed solution, and pulp 101 parts by weight of 2.4.5-trichloroaniline into 248 mesh fineness through colloid mill After adding in the mixed solution, then the concentration of 178 parts by weight is that 30.5% hydrochloric acid, 14 parts by weight of octadecyl dimethyl hydroxyethyl quaternary ammonium nitrate are added in the mixed solution, beating for 1 hour, and use The concentration of 113 weight parts is the diazotization of 30.5% sodium nitrite solution, makes diazonium liquid;
[0036] b. Preparation of naphthol AS-D alkaline solution: Add 138 parts by weight of NaOH with a concentration of 30.5% to 1000 parts by weight of water, heat up to 92°C, add 11 parts by weight of rosin resin and keep it for 0.1 hour, add 1...
PUM
![No PUM](https://static-eureka.patsnap.com/ssr/23.2.0/_nuxt/noPUMSmall.5c5f49c7.png)
Abstract
Description
Claims
Application Information
![application no application](https://static-eureka.patsnap.com/ssr/23.2.0/_nuxt/application.06fe782c.png)
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com