Treatment method of diacyl peroxide
A treatment method and peroxide technology, which are applied in chemical instruments and methods, preparation of organic compounds, alkali metal chlorides, etc., can solve the problems of changing the molecular structure of BPO, having no practical use value, and being unable to be marketed or applied. Achieve the effect of reducing solid waste generation, good treatment effect and increasing reaction specific surface
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Embodiment 1
[0048]600kg water, 78kg sodium hydroxide solution (32 wt%), 6 kg of sodium dodecyl amyl sulfonate (2 wt%), 120 kg peroxidation (binated) benzoyl ablation (containing 0.3 kmol peroxidation (b) beyemr Aoy) is added to 1000 L of the reaction kettle, and after mixing, the mass content of the mixture (sodium hydroxide in the mixed material is 3.6%, the mass content of sodium dodecyl benzene sulfonate in the mixture is 0.017%) ;
[0049]When the jacket was warmed, the temperature reached 65 ° C, the resulting dispersion material started to perform an oxidative reaction, and the control reaction temperature was 70 ° C, and the temperature was 5 h, and then the cooling water was opened in the reactor to cool down, cooled to 20 ° C, resulting in product material;
[0050]The product material was sent to the centrifuge for the first separation (the centrifugal rotary speed was 1000 rpm, the centrifugal time was 10 min), and the peroxidation of the insoluble material and the first filtrate, the pero...
Embodiment 2
[0054]600 kg of water, 82 kg of sodium hydroxide solution (32 wt%), 6 kg of sodium dodecylbenzene sulfonate (2 wt%), 120 kg peroxidation (di) benzoylum waste was added to the 1000L reactor, and after mixing, The quality content of the mixture (sodium hydroxide in the mixture is 3.8%, the mass content of sodium dodecylbenzene sulfonate in the mixture is 0.017%);
[0055]When the jacket was warmed, the temperature reached 65 ° C, the resulting dispersion material started to perform an oxidative reaction, the control reaction temperature was 70 ° C, heat preservation of 4 h, then opened the cooling water in the reaction kettle to cool down, cooled to 20 ° C, resulting in product material;
[0056]The product material was sent to the centrifuge for the first separation (the centrifugal rotary speed was 1000 rpm, the centrifugal time was 10 min), and the peroxidation of the insoluble material and the first filtrate, the peroxidation (b) benzoyl content in the insoluble matter was 0%, Completel...
Embodiment 3
[0060]600kg of water, 78kg sodium hydroxide solution (32 wt%), 6 kg of sodium dodecylpylsulfonate (2 wt%), 120 kg peroxidation (di) benzoylum waste was added to 1000L reactor, and after mixing, The quality content of the mixture (sodium hydroxide in the mixture is 3.6%, the mass content of sodium dodecyl benzene sulfonate in the mixture is 0.017%);
[0061]When the jacket was warmed, the temperature was reached at 65 ° C, the obtained dispersion material was redox, and the control reaction temperature was 70 ° C, the temperature was 8 h, and then the cooling water was cooled in the reaction kettle to cool down, cooled to 20 ° C, resulting in product material;
[0062]The product material was sent to the centrifuge for the first separation (the centrifugal rotary speed was 1000 rpm, the centrifugal time was 10 min), and the peroxidation of the insoluble material and the first filtrate, the peroxidation (b) benzoyl content in the insoluble matter was 0%, Completely reactive;
[0063]To the fir...
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