Method for preparing anthraquinone
An anthraquinone and process technology, applied in the field of anthraquinone preparation, can solve problems such as environmental pollution, achieve the effects of reducing environmental pollution, reducing comprehensive preparation costs, and increasing yield
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[0034] The invention provides a preparation method of anthraquinone, which comprises steps of condensation, hydrolysis, ring closure and dilution;
[0035] Condensation process
[0036] In the application, the condensation process is:
[0037] According to the weight ratio of benzene: aluminum trichloride: phthalic anhydride = 1: (2-10): (1-6), first send benzene into the condensation kettle, start stirring and add aluminum trichloride, and then put in phthalic anhydride. Keep the temperature in the kettle at 20-50°C to make the reaction completely generate aluminum o-benzoylbenzoate. After the reaction, raise the temperature to 55-65°C and keep it warm for 1-5 hours;
[0038] As a preferred technical scheme, the condensation process is:
[0039] According to the weight ratio of benzene: aluminum trichloride: phthalic anhydride = 1:3-4:2, first send benzene into the condensation kettle, start stirring and add aluminum trichloride, then put in phthalic anhydride, and keep th...
Embodiment 1
[0076] Embodiment 1 provides a preparation method of anthraquinone, including condensation, hydrolysis, ring closure, dilution process, mother liquor retreatment process, waste sulfuric acid water retreatment process.
[0077] Condensation process
[0078] According to the weight ratio of benzene: aluminum trichloride: phthalic anhydride = 1:3.4:2, first send benzene into the condensation kettle, start stirring and add aluminum trichloride, and then put in phthalic anhydride. Make the reaction completely generate aluminum o-benzoylbenzoate, heat up to 60°C after the reaction, and keep the temperature for 1 hour;
[0079] Hydrolysis process
[0080] a. Hydrolysis and acidification: put the aluminum phthaloylbenzoic acid salt that has completed the condensation reaction into a hydrolysis kettle filled with bottom water, add dilute sulfuric acid with a mass concentration of 10%, and react to generate o-benzoylbenzoic acid;
[0081] b. Separation: after the completion of the ...
Embodiment 2
[0102] Embodiment 2 provides a preparation method of anthraquinone, including condensation, hydrolysis, ring closure, dilution process, mother liquor retreatment process, waste sulfuric acid water retreatment process.
[0103] The difference between embodiment 2 and embodiment 1 is the hydrolysis process, and the hydrolysis process of embodiment 2 is:
[0104] Hydrolysis process
[0105] a. Hydrolysis and acidification: put the aluminum phthaloylbenzoic acid salt that has completed the condensation reaction into a hydrolysis kettle filled with bottom water, add dilute sulfuric acid with a mass concentration of 10%, and react to generate o-benzoylbenzoic acid;
[0106] b. Separation: after the completion of the reaction, carry out static layering, and discharge the lower layer mother liquor from the bottom of the reaction kettle after layering, so as to stay in the benzene-soluble o-benzoylbenzoic acid at the bottom of the reaction kettle; collect the lower layer mother liquo...
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