Process for separating and utilizing mixing components of o-, m-, and p-nitrochlorobenzene
A technology of p-nitrochlorobenzene and o-nitrochlorobenzene, which is applied in the field of green and sustainable development separation and utilization engineering, can solve the problems of large investment, high cost, and secondary pollution, and achieve energy saving and consumption reduction, environmental pollution, and easy Separation and purification, the effect of high use value
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Embodiment 1
[0030] Add 157.5 kg of industrial production residues of p- and o-nitrochlorobenzene in the reaction kettle, add 1.58 kg of aluminum trichloride, heat to 80 ° C, and pass 15.8 kg of chlorine gas for about 8 hours for chlorination. Return the unchlorinated monochloronitrobenzene compound for rechlorination, and the product produced by chlorination is mixed dichloronitrobenzene: 3,4-dichloronitrobenzene, 2,5-dichloronitrobenzene, 2 , 4-dichloronitrobenzene, 2,3-dichloronitrobenzene. Then according to the difference in boiling point, 2.4 kg of 2,3-dichloronitrobenzene was separated by a rectification tower, and its purity was ≥99.5% as detected by gas chromatography, with a melting point of 62°C and a yield of about 1.3%; simultaneously, 2,4-dichloronitrobenzene was obtained. The mixture of chloronitrobenzene, 2,5-dichloronitrobenzene and 3,4-dichloronitrobenzene was 45.6 kg, and the yield was about 23.8%.
Embodiment 2
[0032] Add 157.5 kg of industrial production residues of p- and o-nitrochlorobenzene into the reaction kettle, add 3.95 kg of aluminum trichloride, heat to 95 ° C, and pass 60 kg of chlorine gas for about 9 hours for chlorination. Return the unchlorinated monochloronitrobenzene compound for rechlorination, and the product produced by chlorination is mixed dichloronitrobenzene: 3,4-dichloronitrobenzene, 2,5-dichloronitrobenzene, 2 , 4-dichloronitrobenzene, 2,3-dichloronitrobenzene. Then, according to the difference in boiling point, 7.2 kg of 2,3-dichloronitrobenzene was separated by a rectifying tower, and its purity was detected by gas chromatography to be ≥99.5%, with a melting point of 62°C and a yield of about 3.8%; at the same time, 2,4-dichloronitrobenzene was obtained. The mixture of chloronitrobenzene, 2,5-dichloronitrobenzene and 3,4-dichloronitrobenzene was 129.6 kg, and the yield was about 67.5%.
Embodiment 3
[0034] Add 157.5 kg of industrial production residues of p- and o-nitrochlorobenzene into the reaction kettle, add 7.87 kg of aluminum trichloride, heat to 105 ° C, and pass 157.5 kg of chlorine gas for about 9 hours for chlorination. Return the unchlorinated monochloronitrobenzene compound for rechlorination, and the product produced by chlorination is mixed dichloronitrobenzene: 3,4-dichloronitrobenzene, 2,5-dichloronitrobenzene, 2 , 4-dichloronitrobenzene, 2,3-dichloronitrobenzene. Then, according to the difference in boiling point, 15.4 kg of 2,3-dichloronitrobenzene was separated by a rectification tower, and its purity was ≥99.5% as detected by gas chromatography, with a melting point of 62°C and a yield of about 8%; at the same time, 2,4-dichloronitrobenzene was obtained. The mixture of chloronitrobenzene, 2,5-dichloronitrobenzene and 3,4-dichloronitrobenzene was 176.6 kg, and the yield was about 92%.
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