Method for recovering o-dichlorobenzene through sulfonation process of bromamine acid produced by solvent method
A technology of o-dichlorobenzene and bromo-amino acid, applied in the direction of disproportionation separation/purification of halogenated hydrocarbons, etc., can solve the problems of high production cost of bromo-amino acid, pollution of organic solvents, high energy consumption, etc.
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Embodiment 1
[0015] Put 100 parts of 1-aminoanthraquinone into 700 parts of o-dichlorobenzene and stir to form a slurry, heat up to 80°C,
[0016] Add 65 parts of chlorosulfonic acid dropwise; after the dropwise addition, slowly raise the temperature to 125-130°C, keep warm for 3 hours for sulfonation reaction; Stand still at 65-75°C for more than 4 hours, and carefully separate the acid layer. Add 50 parts of sulfuric acid to the ortho-dichlorobenzene layer for washing, and separate the washing acid and o-dichlorobenzene at rest; combine the separated acid layer and washing acid, vacuumize to make the vacuum degree reach -60 kPa, heat to 90°C, and depressurize Recover ortho-dichlorobenzene by distillation. The 1-aminoanthraquinone-2-sulfonic acid sulfuric acid solution that evaporates o-dichlorobenzene can be directly brominated. A total of 696.5 parts of ortho-dichlorobenzene were separated and recovered by vacuum distillation, with a recovery rate of 99.5%.
[0017]
Embodiment 2
[0019] Same as Example 1, changed to add 350 parts of 98% sulfuric acid, and a total of 689 parts of o-dichlorobenzene were recovered, with a recovery rate of 98.4%.
[0020]
Embodiment 3
[0022] Same as Example 1, changed to add 450 parts of 96% sulfuric acid, and a total of 694 parts of o-dichlorobenzene were recovered, with a recovery rate of 99.1%.
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