Cyclic Siloxane Coating Composition for Fluorine-Free Water Repellency

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Solution Overview

Problem

Traditional water-repellent fabrics rely on fluorochemicals, which are undesirable in some applications, prompting the need for fluorine-free alternatives with effective water-repellent properties.

Innovation Solution

Cyclic siloxane compounds with specific structures are applied to fibrous substrates to create hydrophobic layers, offering superior water-repellent properties without using fluorine, achieved through their unique co-crystallization of hydrocarbon chains.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If fluorochemicals are used to create water-repellent fabrics, then water-repellent properties are achieved, but environmental and health concerns arise making them undesirable

Engineering Contradiction:
Improvewater-repellent propertiesVSAvoidfluorine content
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The invention changes the chemical composition parameters by replacing fluorine-containing compounds with cyclic siloxane compounds that have specific molecular structures (Formula I and II), thereby maintaining water-repellent functionality while eliminating harmful fluorine content

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention uses composite material structures where cyclic siloxane molecules form organized assemblies with hydrocarbon chains that co-crystallize, creating a composite material system that achieves superior water repellency without fluorine

Inventive Principle:
Principle #40Composite materials

2Object-affected harmful factors

If traditional hydrocarbon compounds are used for water repellency, then fluorine-free treatment is achieved, but water-repellent properties are insufficient

Engineering Contradiction:
Improvefluorine-freeVSAvoidwater-repellent properties
Core Design Contradiction:
Object-affected harmful factorsVSReliability

Solution Approach 1:

The invention creates a composite material system where cyclic siloxane backbone structures combine with organized hydrocarbon chains that co-crystallize, forming a composite structure that achieves superior water repellency compared to simple hydrocarbon compounds

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The invention applies local quality enhancement by creating specific organized structures of hydrocarbon chains attached to cyclic siloxane backbones, where the local arrangement and co-crystallization of chains provide enhanced water-repellent properties at the molecular level

Inventive Principle:
Principle #3Local quality

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 cyclic siloxane compounds demonstrate excellent water-repellent properties, as evidenced by higher contact angles compared to traditional hydrocarbon compounds, making them suitable for fluorine-free treatments that enhance substrate water repellency.

Implementation Method 1

achieved through their unique co-crystallization of hydrocarbon chains

Methodology Applied
Scientific EffectCo-crystallization: Crystallisation

Implementation Method 2

a layer on which a water droplet has a contact angle of at least 90 degrees

Methodology Applied
Scientific EffectHydrophobicity: Hydrophobe

Data Source

PatentEP3684779B1Cyclic siloxanes, compositions, methods, and articles
Publication Date: 2022.03.23 3M INNOVATIVE PROPERTIES CO
  • EP3684779B1 patent drawing
  • EP3684779B1 patent drawing
  • EP3684779B1 patent drawing

AI summary

A cyclic siloxane compound, composition, method, and an article including the siloxane, wherein the cyclic siloxane has the following Formula (I): wherein: each R1 and R2 is independently a (C1-C4)alkyl; each L1 and L2 is independently a single bond, an alkylene, or an alkylene bonded to a group selected from oxy, thio, carbonyl, -NH-, and combinations thereof; each R3 is independently a linear (C14-C100)alkyl; each R4 is independently a (C1-C30)alkyl, a (C2-C30)heteroalkyl having at least one oxygen, sulfur, or -NH- group, or a (C1-C30)alkyl substituted with a fluoro, thiol, isocyanato, cyanato, hydroxyl, glycidoxy, or epoxy group; with the proviso that L1, L2, and R4 are selected such that each Si atom is directly bonded to an alkylene or an alkyl; m is an integer of at least 2; n is an integer of 0 or above; m + n is an integer of at least 3; and the cyclic siloxane compound is a solid at 25°C.