PGDB Plasticizer for Polyurethane Compatibility and Strength

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Solution Overview

Problem

Traditional plasticizers used in polyurethane formulations often face issues such as volatility, migration, discoloration, and reduced mechanical properties, necessitating the need for alternative plasticizers that offer improved compatibility, color stability, and mechanical strength.

Innovation Solution

The use of 1,2-propylene glycol dibenzoate (PGDB) as a low hydroxyl dibenzoate plasticizer, which is added during the reaction of isocyanate and polyol in reactive polyurethane systems, providing enhanced compatibility, hardness, tensile strength, and optical clarity while minimizing exudation and yellowing.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If traditional plasticizers are used in polyurethane formulations, then processability and flexibility are improved, but volatility, migration, discoloration, and reduced mechanical properties occur

Engineering Contradiction:
ImproveprocessabilityVSAvoidmechanical properties
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The patent changes the chemical parameters of the plasticizer by using dibenzoate esters with specific molecular weight ranges (300-600 g/mol) and controlled hydroxyl numbers (5-30 mg KOH/g). This parameter optimization allows the plasticizer to maintain compatibility and mechanical properties while reducing volatility and migration compared to traditional high-molecular-weight plasticizers

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention uses composite ester structures combining aromatic dibenzoate cores with aliphatic or alicyclic ester chains. This composite structure provides both the compatibility needed for processability and the structural integrity required for maintaining mechanical properties, resolving the contradiction between ease of operation and reliability

Inventive Principle:
Principle #40Composite materials

2Ease of operation

If traditional plasticizers are used in polyurethane formulations, then flexibility is improved, but discoloration and yellowing occur

Engineering Contradiction:
ImproveflexibilityVSAvoiddiscoloration
Core Design Contradiction:
Ease of operationVSObject-generated harmful factors

Solution Approach 1:

The patent introduces local quality by incorporating aromatic dibenzoate ester groups that provide UV stability and color resistance in specific regions of the polymer chain, while the aliphatic ester portions maintain flexibility. This localized functional distribution allows the plasticizer to provide flexibility without the harmful discoloration effect

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The invention converts the potential harm of aromatic structures (which can cause yellowing) into a benefit by using dibenzoate esters with specific molecular weights and hydroxyl numbers. The aromatic core provides UV absorption and color stability, while the controlled ester chain length and low hydroxyl content prevent the yellowing that typically occurs with aromatic plasticizers, thus converting a potential harm into a benefit

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

3Stability of the object's composition

If traditional plasticizers are used in polyurethane formulations, then compatibility is improved, but exudation and migration occur

Engineering Contradiction:
ImprovecompatibilityVSAvoidexudation
Core Design Contradiction:
Stability of the object's compositionVSLoss of substance

Solution Approach 1:

The patent optimizes the molecular weight parameter of the dibenzoate plasticizer to fall within 300-600 g/mol, which is high enough to reduce volatility and migration but low enough to maintain compatibility with the polyurethane matrix. The hydroxyl number is controlled at 5-30 mg KOH/g to ensure hydrogen bonding compatibility while minimizing exudation

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention creates a plasticizer structure that mimics the polyurethane polymer chain structure, with dibenzoate ester groups that can form hydrogen bonds similar to the urethane linkages in the polymer. This structural copying enhances compatibility at the molecular level, preventing phase separation and subsequent exudation

Inventive Principle:
Principle #26Copying

Data Source

PatentEP3814394B1Improved reactive polyurethane systems
Publication Date: 2023.06.14 EMERALD KALAMA CHEMICAL LLC
  • EP3814394B1 patent drawingFigure 1(a)
  • EP3814394B1 patent drawingFigure 1(b)
  • EP3814394B1 patent drawingFigure 2(a)~2(b)

AI summary

Low hydroxyl value dibenzoate plasticizer for use in a reactive polyurethane composition, including but not limited to thermoplastic and thermoset polyurethanes, wherein the plasticizer is particularly useful in TPU's, a reactive polyurethane adhesive or sealant, or a castable polyurethane article and achieves comparable or improved properties, including without limitation compatibility, color, exudation, optical properties, MVTR, hardness, tensile strength, tear strength, rebound, compression set, and solvent swell, when compared with that achieved with traditional plasticizers, including other benzoate esters, used in polyurethane compositions.