Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Two-dimensional or quasi-two-dimensional polymer film synthesis method, two-dimensional or quasi-two-dimensional polymer film and application thereof

A polymer film, monomer polymerization technology, applied in the field of film production, electronic devices or catalysts, can solve the problems of small crystal domain size, reliable function limitation, unsatisfactory crystallinity of 2D polymers, etc.

Pending Publication Date: 2022-06-21
DRESDEN UNIVERSITY OF TECHNOLOGY
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0015] Disadvantageously, the crystallinity of the resulting 2D polymers remains unsatisfactory with small domain sizes (typically tens of nanometers), which poses a potential limitation to the development of reliable functionalities for this emerging class of organic 2D materials.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Two-dimensional or quasi-two-dimensional polymer film synthesis method, two-dimensional or quasi-two-dimensional polymer film and application thereof
  • Two-dimensional or quasi-two-dimensional polymer film synthesis method, two-dimensional or quasi-two-dimensional polymer film and application thereof
  • Two-dimensional or quasi-two-dimensional polymer film synthesis method, two-dimensional or quasi-two-dimensional polymer film and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0122] Formation of surfactant monolayers

[0123] Dissolve 20 μL of sodium oleyl sulfate (SOS) (1 mg ml in chloroform) -1 ) on the surface of 100 ml of Milli-Q water in a 200 ml beaker. The average molecular area (mma) is It can be calculated by the following formula:

[0124]

[0125] In the formula, Ae=25.12cm 2 , is the effective area; M w =M w,sos =370.5g mol -1 , is the molecular weight of SOS; Na=6.02×10 23 mol -1 is Avogadro's constant; m=m sos = 20 μg, which is the mass of the surfactant. The mma allows SOS molecules to form monolayers such as Figure 3A confirmed by the π-A isotherm in .

[0126] Similar to SOS, 15 μl stearic acid (SA, 1 mg ml in chloroform -1 ) was distributed at the interface between air and 100 ml of Milli-Q water. mma is allows SA molecules to form monolayers such as Figure 3B confirmed by the π-A isotherm in .

[0127] Horizontal synthesis of 2D polyimide (2DPI) on water

[0128] To synthesize 2DPI, SOS monolayers wer...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
thicknessaaaaaaaaaa
thicknessaaaaaaaaaa
thicknessaaaaaaaaaa
Login to View More

Abstract

The present invention relates to a method for synthesizing a two-dimensional or quasi-two-dimensional polymer comprising a surfactant, a two-dimensional or quasi-two-dimensional polymer film and use for producing a film, an electronic device or a catalyst.

Description

technical field [0001] The present invention relates to a method for synthesizing two-dimensional or quasi-two-dimensional polymers comprising surfactants, two-dimensional or quasi-two-dimensional polymer membranes and their use for the production of membranes, electronic devices or catalysts. Background technique [0002] Both synthetic and natural polymers play an important and ubiquitous role in our everyday life, and according to the definition proposed by Hermann Staudinger in the early 1920s (Staudinger 1920), they can often be linked linearly by covalent bonds. The repeating unit sequence is described. [0003] There have been numerous attempts to go beyond Staudinger's concept to synthesize sheet polymers with long-range order along two orthogonal directions, namely two-dimensional (2D) polymers, which can be traced back to Gee's interfacial polymerization experiment in 1935 (Gee 1935) , 1958 Blumstein cross-linked polymers in the interlayer space of smectite clays ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C08G73/02C08G73/10C08G73/06C08G69/32C08J5/18
CPCC08G73/0266C08G73/1067C08G73/1085C08G73/0627C08G73/06C08G69/32C08J5/18C08J2377/06C08J2379/08
Inventor 冯新亮董人豪刘珂君
Owner DRESDEN UNIVERSITY OF TECHNOLOGY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products