Hyperbranched Siloxane Polyoxamide Copolymers for Tensile Strength

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Solution Overview

Problem

Siloxane polymers lack tensile strength and the production of highly branched polydiorganosiloxane polyoxamide segmented copolymers is challenging due to difficulties in finding suitable reaction conditions for high degrees of polymerization, particularly with larger polyorganosiloxane segments, and existing methods like dendrimers are tedious and expensive.

Innovation Solution

Hyperbranched polydiorganosiloxane polyoxamide segmented copolymers are synthesized via a one-step, one-pot reaction using a mixture of AXg and BZm compounds, where X and Z are functional groups that react without additional functional groups, facilitating the formation of highly branched structures.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Strength

If block copolymers are formed to improve tensile strength of siloxane polymers, then tensile strength is improved, but the complexity of polymer structure increases

Engineering Contradiction:
Improvetensile strengthVSAvoidpolymer structure complexity
Core Design Contradiction:
StrengthVSDevice complexity

Solution Approach 1:

The patent creates block copolymers combining siloxane segments with polyamide or polyurea segments. The siloxane blocks provide flexibility and low glass transition temperature, while the polyamide/polyurea blocks contribute tensile strength through hydrogen bonding and rigid structure. This composite approach resolves the contradiction by integrating materials with complementary properties to achieve both strength and flexibility.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The patent divides the polymer into distinct soft segments (siloxane) and hard segments (polyamide or polyurea). This segmentation allows each block to perform its specialized function - the soft segments provide flexibility and the hard segments provide strength - thereby achieving high tensile strength without requiring the entire polymer structure to be complex.

Inventive Principle:
Principle #1Segmentation

2Quantity of substance

If condensation reactions are used to produce siloxane-based polyamides, then polyamides are formed, but finding suitable reaction conditions for high degrees of polymerization is difficult

Engineering Contradiction:
Improvedegree of polymerizationVSAvoidreaction conditions
Core Design Contradiction:
Quantity of substanceVSEase of manufacture

Solution Approach 1:

The patent employs specific reaction parameters including elevated temperatures (60-150°C), controlled molar ratios of monomers, and extended reaction times (2-24 hours). These parameter changes optimize the condensation reaction to achieve high degrees of polymerization while maintaining ease of manufacture through straightforward heating and stirring procedures.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent uses coupling agents such as silanes or siloxanes with reactive functional groups that facilitate the condensation reaction between polyamides and siloxane segments. These intermediaries enable efficient bond formation and high molecular weight polymer production under mild reaction conditions, resolving the difficulty of achieving high polymerization degrees.

Inventive Principle:
Principle #24Intermediary (Mediator)

3Quantity of substance

If polydiorganosiloxane segments are increased in size, then soft segment fraction increases, but solubility parameters mismatch makes high degree of polymerization difficult

Engineering Contradiction:
Improvesoft segment fractionVSAvoidsolubility compatibility
Core Design Contradiction:
Quantity of substanceVSEase of manufacture

Solution Approach 1:

The patent introduces intermediate blocks or transition zones between the polydiorganosiloxane soft segments and the polyamide hard segments. These intermediate regions have solubility parameters that bridge the gap between the two immiscible phases, allowing for high soft segment fractions while maintaining overall polymer solubility and processability through localized compositional gradients.

Inventive Principle:
Principle #3Local quality

4Device complexity

If linear or branched polydiorganosiloxane polymers are used, then polymer structure is simple, but tensile strength remains low

Engineering Contradiction:
Improvepolymer structure simplicityVSAvoidtensile strength
Core Design Contradiction:
Device complexityVSStrength

Solution Approach 1:

The patent transforms simple linear or branched siloxane polymers into composite block copolymers by incorporating polyamide or polyurea blocks. The siloxane portions maintain the simple structure and flexibility, while the added polyamide/polyurea blocks provide the necessary tensile strength through their rigid, hydrogen-bonded networks, achieving strength enhancement without complicating the base siloxane architecture.

Inventive Principle:
Principle #40Composite materials

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 hyperbranched copolymers exhibit unique properties such as optical transparency, high moisture vapor transmission, thermal stability, and solubility in a wide range of solvents, with improved melt behaviors and functionalization capabilities.

Implementation Method 1

hyperbranched polymers prepared from the reaction mixture comprising: AXg and BZm wherein each X comprises either an oxalylamino-functional group of the formula: -NH-(CO)-(CO)-OR

Methodology Applied
Scientific EffectCondensation reaction:

Data Source

PatentEP3676313B1Hyperbranched polydiorganosiloxane polyoxamide polymers
Publication Date: 2026.04.22 3M INNOVATIVE PROPERTIES CO
  • EP3676313B1 patent drawing
  • EP3676313B1 patent drawing
  • EP3676313B1 patent drawing

AI summary

Hyperbranched polydiorganosiloxane polyoxamide polymers are formed from reaction mixtures containing AXg and BZm compounds where either A or B is a siloxane-based group, and each X is either an oxalylamino-functional group or an amino-functional group, and each Z is either an amino-functional group or an oxylamino-functional group, such that upon reaction X and Z form an oxamide bond.