Halogen-Free Polyarylene Sulfide Synthesis via Catalyst Substitution

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Solution Overview

Problem

Conventional methods for preparing polyarylene sulfide (PAS) and polythioether sulfone (PTES) involve halogen-containing processes, resulting in low yields and environmental pollution due to unrecyclable halogen-containing byproducts.

Innovation Solution

A method involving the reaction of compounds represented by specific formulas in the presence of halogen-free catalysts and solvents, eliminating the need for halogen-containing side product removal and enhancing product yield and molecular weight.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If halogen-containing processes are used to prepare polyarylene sulfide and polythioether sulfone, then the polymerization can proceed, but the yield is low and halogen-containing byproducts cause environmental pollution

Engineering Contradiction:
ImproveyieldVSAvoidhalogen-containing byproducts
Core Design Contradiction:
ProductivityVSObject-generated harmful factors

Solution Approach 1:

The patent changes the chemical parameters of the reaction system by replacing halogen-containing reagents with halogen-free alternatives. Specifically, it uses non-halogenated aromatic compounds as starting materials and employs catalysts that do not contain halogen, fundamentally altering the reaction pathway to eliminate halogen-containing byproducts while maintaining polymerization efficiency and improving yield

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent converts the harmful halogen-containing process into a beneficial halogen-free process. By deliberately choosing halogen-free starting materials and catalysts, the method transforms what was previously a source of pollution (halogen reagents) into an environmental advantage, producing no halogen-containing waste while achieving high yields

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

2Ease of manufacture

If halogen-containing processes are used, then polymerization occurs, but additional steps are required to remove halogen-containing side products, increasing complexity and cost

Engineering Contradiction:
Improveprocess simplicityVSAvoidprocess steps
Core Design Contradiction:
Ease of manufactureVSDevice complexity

Solution Approach 1:

The patent extracts and eliminates the harmful halogen-containing components from the entire process. By removing halogen-containing reagents, catalysts, and intermediates from the reaction system, the method eliminates the need for subsequent removal steps, simplifying the overall manufacturing process while maintaining product quality

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

Instead of performing polymerization with halogen-containing reagents and then removing the harmful byproducts (the conventional approach), the patent inverts the logic by starting with halogen-free reagents from the beginning. This reversal eliminates the need for removal steps entirely, simplifying the process

Inventive Principle:
Principle #13The other way round (Inversion)

3Reliability

If conventional halogen-containing methods are used, then polymerization can proceed, but molecular weight and polydispersity index are not optimized

Engineering Contradiction:
Improvepolymer qualityVSAvoidmolecular weight control
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The patent optimizes polymer quality by changing the reaction parameters to halogen-free conditions. This includes using halogen-free catalysts, controlling reaction temperature and time, and selecting appropriate halogen-free solvents or solvent-free conditions. These parameter changes result in improved molecular weight control and reduced polydispersity index, enhancing overall polymer quality

Inventive Principle:
Principle #35Parameter changes

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 produces halogen-free monomers and polymers with increased molecular weight and reduced polydispersity index, reducing preparation costs and environmental impact.

Implementation Method 1

A compound having a structure represented by Formula (I) is reacted with a compound having a structure represented by Formula (III) in the presence of a compound having a structure represented by Formula (II), obtaining a compound having a structure represented by Formula (IV)

Methodology Applied
Scientific EffectChemical reaction: Chemical Bonding

Implementation Method 2

The compound having the structure represented by Formula (IV) is reacted with a compound (A), obtaining a compound having the structure represented by Formula (V). The compound (A) is nitric acid, sulfuric acid, acetic acid, hydrogen peroxide, or a combination thereof

Methodology Applied
Scientific EffectChemical reaction: Chemical Bonding

Implementation Method 3

The compound having the structure represented by Formula (V) is reacted with a compound having a structure represented by Formula (VI), obtaining a polymer having a repeat unit represented by Formula (VII)

Methodology Applied
Scientific EffectPolymerization: Photopolymerisation

Data Source

PatentUS10723841B2Method for preparing compound and method for preparing polymer employing the same
Publication Date: 2020.07.28 IND TECH RES INST
  • US10723841B2 patent drawing
  • US10723841B2 patent drawing
  • US10723841B2 patent drawing

AI summary

A method for preparing a compound and a method for preparing a polymer employing the same are provided. The method for preparing a compound includes reacting a compound having a structure represented by Formula (I) with a compound having a structure represented by Formula (III) in the presence of a compound having a structure represented by Formula (II) to obtain a compound having a structure represented by Formula (IV)wherein Ar1 is substituted or unsubstituted aryl group; X is —O—, —S—, or —NH—; R1 is independently hydrogen or C1-6 alkyl group; R2 is hydroxyl group, C1-6 alkyl group, phenyl group, or tolyl group; and R3 is independently C1-6 alkyl group, C5-8 cycloalkyl group, or C2-6 alkoxyalkyl group.