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Reaction device and method for synthesizing phthalic anhydride

A phthalic anhydride, reaction device technology, applied in chemical instruments and methods, organic chemistry, chemical/physical processes, etc., can solve the problems of unstable operation, large floor space, large equipment investment, etc., and achieve equipment investment. The effect of large size, large floor space and high processing energy consumption

Active Publication Date: 2020-12-04
SHANXI INST OF COAL CHEM CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] For the preparation of phthalic anhydride by fixed bed and other processes currently used, the preparation process equipment has large investment, large floor space, high energy consumption for treatment, unstable operation and other problems. The present invention provides a reaction for the synthesis of phthalic anhydride Apparatus and method

Method used

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  • Reaction device and method for synthesizing phthalic anhydride
  • Reaction device and method for synthesizing phthalic anhydride
  • Reaction device and method for synthesizing phthalic anhydride

Examples

Experimental program
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Embodiment 1

[0027] A reaction device for synthesizing phthalic anhydride, comprising a reactor 1 and a heating device 3 for heating the reactor 1, the upper surface of the heating device 3 is provided with a container 2 for holding a heating medium, the Reactor 1 is a "U" type reactor composed of feed pipe 101, secondary reaction chamber 102, main reaction chamber 103 and discharge pipe 104. Said secondary reaction chamber 102 is arranged outside container 2, said main reaction chamber 103 is arranged in the container 2, and the two ends of the reaction tube extend to the outside of the container 2. By adjusting the lengths of the secondary reaction chamber 102 and the main reaction chamber 103, the reaction liquid is fully contacted with the solid catalyst and then left for a required reaction time before flowing out.

Embodiment 2

[0029] This embodiment synthesizes bio-based phthalic anhydride, and the reaction steps are as follows:

[0030] Step 1: Filling of the solid catalyst: take two 0.6g Amberlyst-15 solid catalysts and fill them in the secondary reaction chamber 102 and the main reaction chamber 103 respectively.

[0031] Step 2: 0.4000g acetic anhydride, 0.0202g internal standard sulfolane, 0.0204g purified furan and the cycloaddition intermediate product of maleic anhydride Diels-Alder reaction are made into a reaction liquid, and input from the feed pipe port with a pipette gun In the reaction chamber, the ratio of the feed pipe 101, the secondary reaction chamber 102, the main reaction chamber 103 and the discharge pipe 104 is 0.5:3:0.5:0.5, and the timing begins when the first drop of the reaction solution touches the reaction chamber, until the first The drop reaction solution flows out of the reaction chamber, which is the retention time of the reaction solution in the reaction chamber. Th...

Embodiment 3

[0045] The method for synthesizing bio-based phthalic anhydride in this embodiment is basically the same as the method in Example 2, and the specific operation steps are as follows:

[0046] Step 1: Filling of the solid catalyst: take two 0.6g Amberlyst-15 solid catalysts and fill them in the secondary reaction chamber 102 and the main reaction chamber 103 respectively.

[0047] Step 2: 0.4000g acetic anhydride, 0.0202g internal standard sulfolane, 0.0206g purified furan and the cycloaddition intermediate product of maleic anhydride Diels-Alder reaction are made into a reaction liquid, and input from the feed pipe port with a pipette gun In the reaction chamber, the ratio of the feed pipe 101, the secondary reaction chamber 102, the main reaction chamber 103 and the discharge pipe 104 is 0.5:2:1:0.5, and the timing begins when the first drop of the reaction solution touches the reaction chamber, until the first drop of the reaction liquid touches the reaction chamber. The drop...

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Abstract

The invention discloses a reaction device and method for synthesizing phthalic anhydride, and belongs to the field of bio-based chemicals. The method comprises steps: reaction liquid is added from thefeeding pipe opening, the reaction liquid and a solid catalyst are kept in full contact for a certain reaction time to flow out by controlling the length of the reaction cavity, a traditional stirrerdoes not need to be adopted for material mixing, catalyst mechanical strength loss caused by magneton stirring is avoided, energy consumption is low, efficient mixing can be achieved, and productionefficiency is improved. The reaction effect is better; when the device is used for producing phthalic anhydride, the operation process is simple, the investment is low, the consumption is low, and a very remarkable resource recovery effect is achieved.

Description

technical field [0001] The invention belongs to the technical field of bio-based chemicals, and in particular relates to a reaction device and method for synthesizing phthalic anhydride. Background technique [0002] Phthalic anhydride, referred to as phthalic anhydride. Its main purpose is to be further derived into dibutyl phthalate, used as a plasticizer for PVC, etc.; it is also widely used in the production of unsaturated polyester resins, alkyd resins, fuels and pigments. [0003] Patent CN101130535A has reported using o-xylene and / or naphthalene as raw materials, using a fixed-bed reactor, and the material flows from top to bottom in the reaction tube bed, and adopts two-stage, three-stage or four-stage bed packing V-Ti type catalyst Preparation of phthalic anhydride. Patent CN110872265A reports that o-xylene is used as a raw material for gasification, using a fixed bed, and the gas passes through A, B, C, D, and catalysts in sequence to prepare phthalic anhydride. ...

Claims

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Application Information

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IPC IPC(8): B01J8/06C07D307/89
CPCB01J8/06C07D307/89
Inventor 邓天昇邵孝杰侯相林
Owner SHANXI INST OF COAL CHEM CHINESE ACAD OF SCI