Process for the separation of diethylbenzene in carbon deka-aromatic hydrocarbons
A carbon ten aromatic hydrocarbon and separation method technology, applied in the field of separation of diethylbenzene, can solve the problems of not finding an efficient adsorbent desorbent, large investment, etc., and achieve good separation effect and thermal stability, low energy consumption, and product purity. high effect
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Embodiment 1
[0013] 1.C 10 Initial separation of mixed diethylbenzene in heavy aromatics
[0014] To C 10 The heavy aromatics reformate raw material undergoes initial fractionation to separate the diethylbenzene component. Some main parameters of the rectification experimental device: rectification column type: packed column with vacuum sleeve for heat insulation; packing material: 2mm θ ring; rectification column size: 30mm×1.5m; kettle capacity: 3000ml; adopts intermittent precision Distillation method, normal pressure operation. Heating and distilling the raw materials in the tower kettle, a condenser is installed on the top of the tower, and the reflux ratio is controlled by a reflux ratio controller. At the beginning, use total reflux and rapid heating to make the liquid in the tower boil quickly. After there is reflux liquid on the top of the tower, adjust the heating power of the tower to make the tower top temperature and reflux stable, and the weight ratio of reflux to outflow is 15:1...
Embodiment 2
[0022] 1.C 10 Initial separation of mixed diethylbenzene in heavy aromatics
[0023] The rectification experiment device is the same as in Example 1. The weight ratio of reflux to outflow is 3:1, and the recovery rate is 30 g / hour. The fractions in the range of 178-182°C were collected, and the content of mixed diethylbenzene was 84.2% by weight.
[0024] 2. Extractive distillation
[0025] The experimental device for extractive distillation is the same as in Example 1. The extractant is dibutyl phthalate: the flow rate is 300 g / h. The feed temperature is ~180℃, the feed position is the upper half of the tower; the raw material concentration: the content of mixed diethylbenzene is 84.2% (weight), the flow rate is 60 g / h, the feed temperature is 150℃, and the feed position is extraction The lower half of the rectification column.
[0026] The mixture of extractant, p-diethylbenzene and a small amount of m-diethylbenzene flows out from the bottom of the column. The m-diethylbenzene ...
Embodiment 3
[0030] 1.C 10 Initial separation of mixed diethylbenzene in heavy aromatics
[0031] The rectification experiment device is the same as in Example 1. The weight ratio of reflux to outflow is 30:1, and the recovery rate is 30 g / h. The fractions in the range of 178-182°C are collected, and the separated mixed diethylbenzene content is 92.5% by weight.
[0032] 2. Extractive distillation
[0033] The experimental device for extractive distillation is the same as in Example 1. The extractant is a mixture of dimethyl phthalate and dibutyl phthalate, and the weight ratio is 1:1: flow rate 800 g / h. The feeding temperature is ~180℃, the feeding position is the upper half of the tower; the raw material concentration: mixed diethylbenzene 92.5% (weight), the flow rate is 40 g / h, the feeding temperature is 150°C, and the feeding position is the extractive distillation column The bottom half.
[0034]The mixture of extractant, p-diethylbenzene and a small amount of m-diethylbenzene flows out ...
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