Silane-Modified Pressure-Sensitive Adhesive for Moisture-Resistant Bonding

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Solution Overview

Problem

Adhesives for glass and ceramic surfaces face challenges with moisture and water, leading to reduced bonding performance and bond failure, especially under high humidity or running water conditions, due to hydrophilic surface properties and the presence of a thin water layer that is difficult to remove.

Innovation Solution

A pressure-sensitive adhesive containing a silane-modified polymer, specifically reacting polymers with acid anhydride or epoxide groups with silanes of a particular formula, which forms a covalent bond with the surface, reducing the water layer and enhancing bonding strength without pre-treatment of the substrate.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If organosilanes are applied to hydrophilic surfaces to create hydrophobicization, then bonding performance is improved, but the process requires pre-treatment steps and waiting periods that delay production

Engineering Contradiction:
Improvebonding performanceVSAvoidwaiting time
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The adhesive formulation incorporates silane-modified polymers that are pre-reacted with glass surface groups during adhesive manufacturing, eliminating the need for separate pre-treatment steps. The silane groups are already activated and ready to bond immediately upon application, removing the 72-hour waiting period required for conventional silane priming processes.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The invention combines the adhesive and silane modification functions into a single integrated adhesive formulation. Instead of applying silane separately before the adhesive, the silane-modified polymer is incorporated into the adhesive itself, merging two separate processes (surface treatment and adhesive application) into one step.

Inventive Principle:
Principle #5Merging (Combining)

2Speed

If reactive silanes are used for rapid hydrophobicization, then bonding speed is improved, but storage stability deteriorates

Engineering Contradiction:
Improvebonding speedVSAvoidstorage stability
Core Design Contradiction:
SpeedVSStability of the object's composition

Solution Approach 1:

The adhesive formulation uses silane-modified polymers with specific silane group distributions. The silane groups are strategically incorporated into the polymer structure at controlled concentrations, providing rapid bonding capability where needed while maintaining overall formulation stability. The local concentration of reactive groups is optimized to balance speed and stability.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The invention uses composite adhesive formulations combining silane-modified polymers with other adhesive components and stabilizers. The composite structure protects the reactive silane groups while maintaining their bonding activity, allowing rapid bonding without sacrificing storage stability over extended periods.

Inventive Principle:
Principle #40Composite materials

3Reliability

If silicone adhesives are used instead of conventional adhesives, then moisture resistance is improved, but cost increases due to expensive materials and special liners

Engineering Contradiction:
Improvemoisture resistanceVSAvoidcost
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The invention modifies the chemical composition parameters of conventional adhesives by incorporating silane-modified polymers. This changes the adhesive's chemical structure to provide moisture resistance similar to silicones, but using more cost-effective polymer materials. The parameter change in composition achieves the desired performance without the high cost of pure silicone systems.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention replaces expensive silicone adhesives and special fluorosiliconized liners with conventional, more economical adhesive materials that have been chemically modified. The silane-modified polymers provide the necessary moisture resistance at lower cost, eliminating the need for expensive special liners while maintaining bond performance.

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

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 adhesive maintains high holding performance on hydrophilic surfaces even under moist conditions, significantly reducing bond failure and extending the holding period under humid and wet environments.

Implementation Method 1

After applying the silane to the hydrophilic surface, a covalent bond is formed between the surface and the silane

Methodology Applied
Scientific EffectCovalent bonding: Chemical Bonding

Implementation Method 2

Adhesion promoters are applied to glasses before bonding, which make the surface hydrophobic and thus eliminate the aforementioned water layer

Methodology Applied
Scientific EffectHydrophobicization: Hydrophobe

Implementation Method 3

Pressure-sensitive adhesives for single- or double-sided pressure-sensitive adhesive strips, which have high holding properties

Methodology Applied
Scientific EffectPressure-sensitive adhesion: Adhesive

Data Source

PatentEP2638119B1Pressure-sensitive adhesives for moisture-insensitive bonds
Publication Date: 2018.05.30 TESA SE
  • EP2638119B1 patent drawingFigure 1
  • EP2638119B1 patent drawing
  • EP2638119B1 patent drawing

AI summary

The invention relates to an adhesive comprising a silane-modified polymer formed from the reaction a) of a polymer containing acid-anhydride or epoxide groups, the epoxide group not being terminal, with b) a silane of the following formula where R1, R2 and R3 independently of one another are selected from the group consisting of methyl, ethyl, 2-methoxyethyl, isopropyl and butyl, m = 0 or 1, n = 0 to 12, p = 1 or 2, and, for p = 1, Y = a functional group selected from the group consisting of glycidyl, glycidyloxy, isocyanato, -NH-CH2-CH2-NR4R5, -NR4R5 (where R4 and R5 independently of one another are selected from the group consisting of H, alkyl, phenyl, benzyl, cyclopentyl and cyclohexyl), and SH, or, for p = 2, Y = NH.