Caprolactam refining method
A technology of caprolactam and a refining method, which is applied in the refining field of caprolactam, can solve the problems of complicated process flow, inability to take into account product quality and yield, poor economy and the like, and achieves the effects of high purity, improved yield and reduced efflux.
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[0026] According to a preferred embodiment of the present invention, the conditions of the vacuum distillation include: a pressure of 0.3-2kPa, a temperature of 50-170°C, and a top reflux ratio of 1:(10-50). The pressures mentioned are absolute pressures.
[0027] According to the present invention, the variable temperature and pressure conditions refer to the gradual increase and decrease of temperature and pressure, and the variable temperature and pressure conditions can also stay at a certain temperature point or a certain pressure point for a period of time, but do not include temperature and pressure. The operation of high and low pressure.
[0028]Since caprolactam is a heat-sensitive substance, the residence time should be as short as possible under high temperature conditions. In addition, in the vacuum distillation process, the loss of caprolactam should be reduced as much as possible. The impurities with lower boiling point (less than 150°C) in the product are remo...
Embodiment 1
[0092] (1) Preparation of the crude product of caprolactam: get 785g of cyclohexanone oxime and carry out the crude caprolactam obtained by gas-phase Beckmann rearrangement reaction, utilize rotary evaporator to carry out solvent (methanol) recovery, obtain 303.5g containing the impurity that boiling point is higher than caprolactam and The caprolactam crude product of the impurity with lower boiling point than caprolactam, the caprolactam crude product is analyzed, and it is known that its main composition is: 95.8% by weight of caprolactam, 4840 μg / g of 5-cyano-1-pentene, 57 μg / g of cyclic Hexanone oxime, cyclohexenone at 4844 μg / g, octahydrophenazine at 386 μg / g, tetrahydroazepin-2-one and its isomers at 132 μg / g, decahydrophene at 1040 μg / g Oxyzine and other unidentified impurities.
[0093] (2) Remove light impurities: Distill the crude product of caprolactam under reduced pressure. Under the pressure (absolute pressure) of 1.3kPa, the temperature is heated from room temp...
Embodiment 2
[0103] (1) Preparation of caprolactam crude product: same as Example 1.
[0104] (2) Remove light impurities: Distill the crude product of caprolactam under reduced pressure, the pressure (absolute pressure) is 1.7kPa, the temperature is heated from room temperature (20°C) at 3°C / min to 90°C for 40min, there is no reflux at the top of the tower, Then the temperature was raised to 160°C at a rate of 3°C / min, the pressure was directly reduced to 0.35kPa, and the top reflux ratio was 1:40, until no light components were distilled out, and 265.8g of light-removed product (bottom material) was obtained. Chromatographic analysis of its main components: 98.9% by weight of caprolactam, 190 μg / g of 5-cyano-1-pentene, 205 μg / g of cyclohexanone oxime, 1023 μg / g of cyclohexenone, 440 μg / g of octahydro Phenazine, 210 μg / g tetrahydroazepin-2-one and its isomers and 1182 μg / g decahydrophenazine.
[0105] (3) Carry out crystallization and refinement according to the method of Example 1. The ...
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