Aromatic Dianhydride Extraction Column Packing

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Solution Overview

Problem

Current methods for producing aromatic dianhydrides result in decreased yields and increased by-product formation due to inefficient extraction processes.

Innovation Solution

A method involving reacting an aromatic diimide with a substituted or unsubstituted phthalic anhydride in an aqueous medium with an amine exchange catalyst, followed by extraction using an organic solvent in a column with a high specific surface area packing material and an interface positioned between 14 to 85% of the column height, effectively converting the aromatic tetraacid salt to dianhydride.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If conventional extraction methods are used to remove phthalimide from the reaction mixture, then the extraction process is simple, but the yield of aromatic dianhydride decreases and by-product formation increases

Engineering Contradiction:
Improvedianhydride yieldVSAvoidby-product formation
Core Design Contradiction:
ProductivityVSObject-generated harmful factors

Solution Approach 1:

The patent changes the physical parameters of the extraction system by using high surface area packing material (increasing the surface area parameter) and optimizing the interface level position (changing the position parameter). These parameter changes improve extraction efficiency, increase dianhydride yield, and reduce by-product formation without complicating the extraction process itself.

Inventive Principle:
Principle #35Parameter changes

2Productivity

If extraction is performed with standard packing material, then the extraction column is simple, but extraction efficiency is insufficient leading to lower dianhydride conversion

Engineering Contradiction:
Improvedianhydride conversionVSAvoidextraction column structure
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent applies porous high surface area packing material in the extraction column. This porous structure provides extensive surface area for mass transfer between phases, significantly improving extraction efficiency and dianhydride conversion. The specific surface area parameter is optimized to enhance extraction performance while maintaining column simplicity.

Inventive Principle:
Principle #31Porous materials

Solution Approach 2:

The patent optimizes the interface level position as a spatial dimension parameter (positioning it at 14-85% of column height). This dimensional optimization creates optimal flow patterns and contact between phases, enhancing extraction efficiency and dianhydride conversion without adding structural complexity.

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

This approach enhances dianhydride conversion and yield, improves extraction efficiency, and reduces by-product formation, achieving higher purity and increased capacity.

Implementation Method 1

removing the phthalimide from the aqueous reaction mixture by extracting the aqueous reaction mixture with an organic solvent

Methodology Applied
Scientific EffectLiquid-liquid extraction: Liquid-Liquid Extraction

Implementation Method 2

reacting an aromatic diimide with a substituted or unsubstituted phthalic anhydride in an aqueous medium in the presence of an amine exchange catalyst

Methodology Applied
Scientific EffectChemical reaction: Chemical Bonding

Data Source

PatentUS11787776B2Method for producing an aromatic dianhydride
Publication Date: 2023.10.17 SHPP GLOBAL TECH BV
  • US11787776B2 patent drawing
  • US11787776B2 patent drawing
  • US11787776B2 patent drawing

AI summary

A method for producing an aromatic dianhydride includes reacting an aromatic diimide with a substituted or unsubstituted phthalic anhydride in an aqueous medium in the presence of an amine exchange catalyst to provide an aqueous reaction mixture including an N-substituted phthalimide, an aromatic tetraacid salt, and at least one of an aromatic triacid salt and an aromatic imide diacid salt. The method further includes removing the phthalimide from the aqueous reaction mixture by extracting the aqueous reaction mixture with an organic solvent and converting to the corresponding aromatic dianhydride. The extracting is carried out in an extraction column including a high specific surface area metal packing material and having an interface between the aqueous reaction mixture and the organic solvent that is at a level that is 14 to 85% of the height of the extraction column.