Method of recovering organic record dye during light record medium producing process
An optical recording medium and organic technology, applied in the direction of organic dyes, azo dyes, chemical instruments and methods, etc., can solve the problems of pollution prevention and control in the optical recording media industry, and achieve the effect of reducing the amount of use
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Embodiment 1
[0034] Take 500 ml of the edge-washing solution of waste optical recording dyes produced in the cyanine-based CD-R process, put it into a beaker, and then evaporate and remove the edge-washing solvent at 35° C. under reduced pressure and vacuum. The evaporated edge washing solvent can be condensed and recovered separately, and then used in the process after distillation and purification. After concentration under reduced pressure, 4 g of solid were obtained. Put the 4 grams of solid in a container, add 20 ml of HPLC grade acetone solvent, and continue shaking the container with a horizontal shaker at a vibration frequency of 180 rpm for 15 hours. At this time, the solid is completely dispersed, and the impurities therein are dissolved in acetone in solvent. Then, the shaken mixture was filtered with filter paper. The solid on the filter paper was washed again with 5 ml of HPLC grade acetone solvent, the washed solid was collected, and 1.6 g of solid was obtained after drying...
Embodiment 2
[0036] Take 500 ml of the waste optical recording dye edging solution produced by the phthalocyanine dye-based CD-R process and put it in a beaker, and then evaporate and remove the edging solvent at 35° C. under reduced pressure and vacuum. After concentration under reduced pressure, 4.66 g of dark green solid was obtained. Put the 4.66 g of solid in a beaker, add 100 ml of ethyl acetate solvent, and heat at 90° C. for 24 hours to dissolve. Filter it with filter paper while it is hot, and let the filtrate stand at room temperature for 24 hours, and a solid precipitates out. The solid and liquid were separated by filter paper, and the obtained solid was dried at 60° C. for 18 hours to obtain 2.46 g of a green solid. The green solid was dissolved again at 90° C. with 6 ml of ethyl acetate, followed by the addition of 12 ml of isopropyl ether, and the solid was recrystallized at room temperature for 18 hours. After filtering again and washing the recrystallized solid on the fi...
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