Nano-structured Polymer Composites via Block Copolymer Self-Assembly

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Solution Overview

Problem

Conventional synthesis methods for nanostructured polymer composites, such as membranes, often require complex material synthesis and struggle to simultaneously achieve thermal stability, mechanical strength, and chemical functionality, limiting their applications in separation and catalytic processes.

Innovation Solution

A process involving a multi-functional monomer and a block copolymer with specific functional groups, reacting in the presence of a metathesis catalyst to form a crosslinked, nano-structured, bicontinuous composite with controlled pore sizes, enabling the creation of robust and functional membranes for separation and catalytic applications.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If conventional synthesis methods are used for nanostructured polymer composites, then material synthesis can be performed, but it is difficult to simultaneously achieve thermal stability, mechanical strength, and chemical functionality

Engineering Contradiction:
Improvechemical functionalityVSAvoidmechanical strength
Core Design Contradiction:
Adaptability or versatilityVSStrength

Solution Approach 1:

The patent employs block copolymer composite materials consisting of distinct chemical segments (e.g., polylactide block and poly(styrene-co-norbornenylethylstyrene) block) that self-organize into nanostructured morphologies. This composite structure enables simultaneous achievement of thermal stability from the rigid matrix, mechanical strength from the crosslinked network, and chemical functionality from the functional groups on the block copolymer chains, resolving the contradiction between versatility and mechanical strength.

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The block copolymer is segmented into distinct functional blocks: one block provides structural stability (thermal and mechanical properties) while the other block provides chemical functionality. This segmentation allows each block to optimize its specific function without compromising the overall performance, enabling simultaneous achievement of mechanical strength and chemical functionality.

Inventive Principle:
Principle #1Segmentation

2Reliability

If conventional synthesis methods are used for nanostructured polymer composites, then material synthesis can be performed, but the synthesis process is complex

Engineering Contradiction:
Improvethermal stabilityVSAvoidsynthesis complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The block copolymer segments self-organize into nanostructured morphologies through spontaneous phase separation driven by incompatibility between distinct chemical segments. This self-organization process eliminates the need for complex external structuring methods, simplifying the synthesis process while reliably producing thermally stable nanostructured composites with controlled morphology.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent controls the nanostructure morphology by adjusting parameters such as block copolymer composition, molecular weight, and crosslinking conditions. By optimizing these parameters, the synthesis process becomes more straightforward and reliable, achieving thermal stability without complex multi-step procedures.

Inventive Principle:
Principle #35Parameter changes

3Shape

If block copolymer segments self-assemble into nanostructured morphology, then structure directing capability is achieved, but control over morphology and pore size is limited

Engineering Contradiction:
Improvenanostructure morphologyVSAvoidpore size control
Core Design Contradiction:
ShapeVSManufacturing precision

Solution Approach 1:

The block copolymer is pre-designed with specific block compositions, molecular weights, and functional groups before assembly. This preliminary design allows precise control over the resulting nanostructure morphology and pore size, as the self-assembly process faithfully reproduces the predetermined block copolymer architecture at the nanoscale, achieving both shape control and manufacturing precision.

Inventive Principle:
Principle #10Preliminary action

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 resulting composite membranes exhibit excellent mechanical properties, thermal robustness, and controlled pore structures, making them suitable for water filtration, gas separation, and catalytic reactions, while maintaining flexibility in copolymer composition and functionality.

Implementation Method 1

reacting in the presence of a metathesis catalyst to form a crosslinked, nano-structured, bicontinuous composite

Methodology Applied
Scientific EffectMetathesis:

Implementation Method 2

The incompatibility of distinct chemical segments leads to nanometer-scale self-organization

Methodology Applied
Scientific EffectSelf-organization: Self-Assembly

Implementation Method 3

the reaction leads to a crosslinked, nano-structured, bicontinuous composite that includes a continuous matrix phase, and a second continuous phase

Methodology Applied
Scientific EffectCrosslinking: Chemical Bonding

Data Source

PatentUS8420704B2Nano-structured polymer composites and process for preparing same
Publication Date: 2013.04.16 REGENTS OF THE UNIVERSITY OF MINNESOTA
  • US8420704B2 patent drawing
  • US8420704B2 patent drawing
  • US8420704B2 patent drawing

AI summary

A process for preparing a polymer composite that includes reacting (a) a multi-functional monomer and (b) a block copolymer comprising (i) a first block and (ii) a second block that includes a functional group capable of reacting with the multi-functional monomer, to form a crosslinked, nano-structured, bi-continuous composite. The composite includes a continuous matrix phase and a second continuous phase comprising the first block of the block copolymer.