Aqueous UV-Curable Ink Monomer for Solubility and Water Resistance

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Solution Overview

Problem

Existing active energy ray-curable inks face issues with monomer stability in aqueous solutions and cured products lacking water resistance.

Innovation Solution

Development of an active energy ray-curable aqueous ink containing a bifunctional polymerizable monomer represented by General Formula (1), which includes a divalent saturated hydrocarbon group with optional ether, amide, carbonyl, sulfone, or sulfonamide bonds, along with a polymerization initiator and optional coloring materials, to enhance water solubility and water resistance.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Quantity of substance

If a conventional monomer is used in aqueous ink, then water solubility is improved, but water resistance of cured product deteriorates

Engineering Contradiction:
Improvewater solubilityVSAvoidwater resistance
Core Design Contradiction:
Quantity of substanceVSReliability

Solution Approach 1:

The patent changes the chemical parameters of the monomer by specifying a bifunctional structure with particular hydrocarbon groups (R1, R2, R3) and functional groups (L) in Formula (1). This structural parameter change enables the monomer to achieve both water solubility in the aqueous ink and water resistance in the cured product, resolving the contradiction between these two properties.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent uses a composite monomer structure combining hydrophilic groups (for water solubility) and hydrophobic groups (for water resistance) within the same molecular framework. The bifunctional monomer of Formula (1) integrates both water-soluble characteristics and water-resistant characteristics, allowing the cured product to exhibit both properties simultaneously.

Inventive Principle:
Principle #40Composite materials

2Ease of manufacture

If a conventional monomer is used in aqueous ink, then ease of manufacture is improved, but monomer stability in aqueous solution deteriorates

Engineering Contradiction:
Improveease of manufactureVSAvoidmonomer stability
Core Design Contradiction:
Ease of manufactureVSStability of the object's composition

Solution Approach 1:

The patent specifies precise structural parameters for the monomer in Formula (1), including the hydrocarbon groups (R1, R2, R3 with specific carbon atom ranges) and functional groups (L with specific bond types). These parameter specifications ensure both ease of manufacture through established synthesis routes and enhanced stability in aqueous solutions by preventing unwanted chemical reactions.

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

The ink achieves improved water solubility and water resistance of the cured product, ensuring stability and effective curing.

Implementation Method 1

an active energy ray-curable aqueous ink containing water and a curable substance and curable by an active energy ray, wherein the curable substance contains a bifunctional polymerizable monomer

Methodology Applied
Scientific EffectPhotopolymerization: Photopolymerisation

Data Source

PatentUS12577417B2Active energy ray-curable aqueous ink, recording method and recording apparatus
Publication Date: 2026.03.17 CANON KK
  • US12577417B2 patent drawing
  • US12577417B2 patent drawing
  • US12577417B2 patent drawing

AI summary

Provided is an active energy ray-curable aqueous ink which contains water and a curable substance and curable by an active energy ray. The curable substance contains a bifunctional polymerizable monomer represented by the following General Formula (1):wherein, R1 is a hydrogen atom or a methyl group, R2 is a divalent saturated hydrocarbon group having 1 to 5 carbon atoms and L is a divalent saturated hydrocarbon group which may contain an ether bond, an amide bond, a carbonyl bond, a sulfone bond or a sulfonamide bond.