Polyaspartic Ester Gel Time Control via Water Content

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Solution Overview

Problem

Polyaspartic ester compositions with a Gel Time shorter than desirable when reacted with polyisocyanates, leading to coatings with long dry-through times and compromised performance properties, and blending fast- and slow-curing compositions does not proportionally improve properties.

Innovation Solution

Careful control of water content in diamine and diester reactant compositions to prepare polyaspartic ester compositions with specific primary amine values and Gel Times, using conditions that maintain low combined water content and selecting diamine and diester compounds to achieve optimal reaction times and properties.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Duration of action of moving object

If polyaspartic esters with hindered secondary amine structure are used to extend Gel Time, then the Gel Time increases, but the dry-through time becomes excessively long and coating performance deteriorates

Engineering Contradiction:
ImproveGel TimeVSAvoiddry-through time
Core Design Contradiction:
Duration of action of moving objectVSProductivity

Solution Approach 1:

The patent changes the chemical parameters of the polyaspartic ester by controlling the water content during synthesis (maintaining less than 0.05% water content) and adjusting the molar ratios of reactants. This produces a polyaspartic ester with primary amine value between 1-30 mg KOH/g, which achieves optimal Gel Time (30-120 minutes) without excessively extending dry-through time, thereby resolving the contradiction between Gel Time extension and productivity maintenance.

Inventive Principle:
Principle #35Parameter changes

2Duration of action of moving object

If chemical structure modification is made to extend Gel Time, then Gel Time increases, but coating performance properties deteriorate

Engineering Contradiction:
ImproveGel TimeVSAvoidcoating performance
Core Design Contradiction:
Duration of action of moving objectVSReliability

Solution Approach 1:

Instead of modifying the chemical structure (which would compromise coating performance), the patent changes the synthesis parameters - specifically controlling water content to less than 0.05% and adjusting reactant ratios. This produces polyaspartic esters with optimized primary amine values that achieve extended Gel Time (30-120 minutes) while maintaining excellent coating performance including hardness, flexibility, and adhesion.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent performs preliminary control of water content during the synthesis stage (before the final coating application). By maintaining water content below 0.05% during polyaspartic ester formation, the reaction produces the desired molecular structure with extended Gel Time properties built-in, rather than requiring post-synthesis modifications that would compromise performance.

Inventive Principle:
Principle #10Preliminary action

3Ease of manufacture

If water content of starting materials is not controlled, then manufacturing is simpler, but Gel Time and physical properties are compromised

Engineering Contradiction:
Improvemanufacturing simplicityVSAvoidGel Time
Core Design Contradiction:
Ease of manufactureVSDuration of action of moving object

Solution Approach 1:

The patent implements preliminary water content control during the synthesis stage by using dry starting materials (water content less than 0.05%) and conducting the reaction under controlled conditions. This preliminary action ensures that the polyaspartic ester formed has the correct molecular structure and primary amine value (1-30 mg KOH/g) to achieve extended Gel Time (30-120 minutes) without requiring complex post-processing or blending operations.

Inventive Principle:
Principle #10Preliminary action

4Duration of action of moving object

If blending fast-curing and slow-curing polyaspartic acid compositions is done, then Gel Time may be adjusted, but the final coating exhibits properties dominated by the slower curing component

Engineering Contradiction:
ImproveGel TimeVSAvoidcoating performance
Core Design Contradiction:
Duration of action of moving objectVSReliability

Solution Approach 1:

The patent extracts the water content variable from the synthesis process and controls it to be less than 0.05%. This extraction of the harmful variable (excess water) allows the polyaspartic ester to achieve extended Gel Time (30-120 minutes) through controlled synthesis rather than through blending different compositions, thereby avoiding the problem where the final coating properties are dominated by the slower curing component.

Inventive Principle:
Principle #2Taking out (Extraction)

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

The controlled polyaspartic ester compositions exhibit extended Gel Times and improved physical properties, such as Shore D Hardness, Chemical Resistance, and Impact Resistance, when reacted with hexamethylene diisocyanate trimer, resulting in high-performance polyurea coatings.

Implementation Method 1

Polyaspartic esters are prepared by reacting a primary amine with maleic or fumaric acid esters in an 'aza'-Michael addition reaction

Methodology Applied
Scientific EffectAza-Michael addition reaction: Chemical Bonding

Implementation Method 2

Polyurea coating compositions are prepared by reacting isocyanate with an amine

Methodology Applied
Scientific EffectPolyaddition reaction: Chemical Bonding

Data Source

PatentUS10717702B2Polyaspartic ester compositions, and methods of making and using same
Publication Date: 2020.07.21 CARGILL INC
  • US10717702B2 patent drawing
  • US10717702B2 patent drawing
  • US10717702B2 patent drawing

AI summary

Methods of preparing a polyaspartic ester composition comprise reacting a primary diamine reactant composition with a diester reactant composition under conditions to prepare a polyaspartic ester composition having a primary amine value of less than 35 mg KOH/g wherein, at the time of the reaction, the combined water content of the primary diamine reactant composition and the diester reactant composition is less than 300 ppm. Compositions and methods of use of the compositions are also described.