Two-Part Cyanoacrylate Adhesive for Deep Cure and Extended Working Time

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Solution Overview

Problem

Conventional single-component cyanoacrylate adhesives face limitations in achieving 'cure through volume' in thicker bondlines and have short working times due to their high reactivity, making it difficult to bond low surface energy substrates with high strength and thermal resistance.

Innovation Solution

A two-part curable composition comprising a first part with a high content of cyanoacrylate monomers and a second part with Michael acceptors and a nucleophilic initiator, allowing for controlled activation and extended working times while maintaining fast fixturing and high bond strength.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Speed

If conventional single-component cyanoacrylate adhesives are used, then rapid bonding and strong adhesion are achieved, but working time is short and cure through volume is limited in thicker bondlines

Engineering Contradiction:
Improvebonding speedVSAvoidworking time
Core Design Contradiction:
SpeedVSLoss of time

Solution Approach 1:

The adhesive system is divided into two separate components: Part A containing cyanoacrylate monomer and Part B containing activator and stabilizer. This segmentation allows the adhesive to remain stable during storage and mixing, then rapidly cure upon contact with the substrate, extending working time while maintaining fast bonding speed.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The activator and stabilizer are pre-mixed in Part B at controlled concentrations. When Part A and Part B are mixed, the activator is immediately available to initiate polymerization upon substrate contact, while the stabilizer is already positioned to control the reaction rate, enabling extended working time without sacrificing cure speed.

Inventive Principle:
Principle #10Preliminary action

2Strength

If conventional single-component cyanoacrylate adhesives are used, then strong adhesion is achieved, but cure through volume is limited in thicker bondlines

Engineering Contradiction:
Improveadhesive bond strengthVSAvoidcure depth in thick bondlines
Core Design Contradiction:
StrengthVSVolume of stationary object

Solution Approach 1:

The activator in Part B serves as an intermediary that bridges the cyanoacrylate monomer and the substrate surface. It enhances the nucleophilic species concentration at the interface, enabling simultaneous initiation of polymerization throughout the adhesive layer, achieving both strong adhesion and complete cure through volume in thick bondlines.

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The invention changes the chemical parameters of the adhesive system by adding activator and stabilizer in specific concentrations. This modifies the polymerization kinetics to enable deep cure through volume while maintaining high bond strength, overcoming the limitation of conventional single-component systems.

Inventive Principle:
Principle #35Parameter changes

3Volume of stationary object

If activators are added to cyanoacrylate composition, then cure through volume is improved, but working time becomes uncontrolled and application becomes complex

Engineering Contradiction:
Improvecure depthVSAvoidapplication simplicity
Core Design Contradiction:
Volume of stationary objectVSEase of operation

Solution Approach 1:

The adhesive and activator/stabilizer are segmented into separate parts that are mixed immediately before application. This eliminates the need for complex pre-activation steps while ensuring proper dosing and stability, simplifying the application process compared to conventional activator methods.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The two-part system is designed to self-regulate the reaction. Upon mixing, the activator automatically initiates polymerization at the optimal moment, and the stabilizer automatically controls the reaction rate. This self-service mechanism eliminates the need for complex external control, maintaining ease of operation while achieving deep cure.

Inventive Principle:
Principle #25Self-service

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 two-part composition achieves long open times, fast fixturing, high bond strength, and thermal resistance, enabling effective bonding of diverse substrates with improved curing depth and resistance to solvents and humidity.

Implementation Method 1

initiation of the polymerisation process occurs from nucleophilic or ionic species found, under normal circumstances, on most surfaces

Methodology Applied
Scientific EffectPolymerization:

Implementation Method 2

initiation of the polymerisation process occurs from nucleophilic or ionic species found, under normal circumstances, on most surfaces

Methodology Applied
Scientific EffectNucleophilic initiation:

Implementation Method 3

a second part (component B) comprising: at least one Michael acceptor M... and a nucleophilic initiator

Methodology Applied
Scientific EffectChemical activation:

Data Source

PatentUS12157784B2Two-part curable composition
Publication Date: 2024.12.03 BOSTIK SA(FR)
  • US12157784B2 patent drawing
  • US12157784B2 patent drawing
  • US12157784B2 patent drawing

AI summary

The present invention concerns a two-part curable composition comprising: ⋅ a first part (component A) comprising at least 51% by weight based on the total weight of the first part, of one or more cyanoacrylate monomer(s), provided that at least one of the cyanoacrylate monomer(s) is a cyanoacrylate monomer comprising a group —X—O—Rb wherein X is a linear or branched alkylene radical optionally interrupted with one or several oxygen atom(s), and Rb is an alkyl group; ⋅ a second part (component B) comprising: at least one Michael acceptor M selected from the group consisting of (meth)acrylic monomers, (meth)acrylic functionalized oligomers, (meth)acrylic functionalized resins, and mixtures thereof, provided that at least one of the Michael acceptor(s) M comprises at least one group of formula —O(CHRa—CH2O)n— where n ranges from 1 to 10 (Michael acceptor M1), and Ra represents CH3 or H; and a nucleophilic initiator.