Preparation method of diazo photosensitizer
A technology of photosensitizer and diazo, which is applied in the direction of photomechanical equipment, photoplate making process of patterned surface, optics, etc., can solve the problems of long period of photosensitizer, poor quality of photosensitizer, and the need for cooling in the preparation process, so as to reduce the Drying steps, short production cycle, reduced synthesis and drying process effects
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Embodiment 1
[0020] Add 320g of concentrated sulfuric acid and 160g of phosphoric acid successively in a 1000ml three-necked flask, cool down in a water bath at room temperature, and gradually add 150g of wet p-aminodiphenylamine diazosulfate (VRT, with a purity of 60-65%), and control the temperature below 40°C. Subsequently, 9 g of paraformaldehyde was added, and the temperature was controlled below 40° C. for 3 h. The reaction solution was slowly added to 1800g of water to dissolve, and 15g of zinc chloride and 92g of sodium chloride were added to precipitate a yellow precipitate, which was filtered and dried to obtain 100g of a photosensitizer product.
Embodiment 2
[0022] Add 275g of concentrated sulfuric acid and 205g of phosphoric acid in sequence to a 1000ml three-neck flask, cool down in a water bath at room temperature, gradually add 150g of wet p-aminodiphenylamine diazosulfate, control the temperature below 40°C, then add 9g of paraformaldehyde, and control the temperature at React below 40°C for 3h. The reaction solution was slowly added to 1600g of water for dissolution, and 15g of zinc chloride and 92g of sodium chloride were added to precipitate a yellow precipitate, which was filtered and dried to obtain 95g of photosensitizer product.
Embodiment 3
[0024] Add 320g of concentrated sulfuric acid and 160g of phosphoric acid in sequence to a 1000ml three-neck flask, cool down in a water bath at room temperature, gradually add 150g of wet p-aminodiphenylamine diazonium chloride salt, control the temperature below 40°C, then add 11g of paraformaldehyde, and control the temperature at React below 40°C for 3h. The reaction solution was slowly added to 1800g of water for dissolution, and 15g of zinc chloride and 92g of sodium chloride were added to precipitate a yellow precipitate, which was filtered and dried to obtain 102g of photosensitizer product.
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