High-strength polymer nanoribbons and preparation method thereof

A polymer and nanoribbon technology, applied in the field of high-strength polymer nanoribbon and its preparation, can solve the problems of increased raw material cost, complex process, low strength of nanoribbon, etc., to achieve industrial production, simple preparation process, excellent mechanical properties performance effect

Active Publication Date: 2014-04-09
CHERY AUTOMOBILE CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] At present, the shapes used as reinforcement materials in composite materials are usually fibers, nanowires, nanotubes, nanoribbons, and nanosheets, among which the fibers are prepared by spinning, while the reinforcement of the other four shapes Materials are prepared in a variety of ways, but are generally complex
Except for a few polymers with low melting point that can be spun by dry spinning, most polymers can only be spun by wet spinning, which requires a large amount of solvent, which increases the cost of raw materials on the one hand, and increases the cost of the process on the other hand.
The synthesis of nanowires and nanotubes generally uses high-temperature chemical vapor deposition, which has complex processes and low yields
[0003] There are various methods for manufacturing nanoribbons in the prior art. For example, people such as Liu publicly reported a method for preparing a polyphenylene vinylene nanoribbon array: adding nano-copper ca

Method used

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  • High-strength polymer nanoribbons and preparation method thereof
  • High-strength polymer nanoribbons and preparation method thereof
  • High-strength polymer nanoribbons and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] (1) Preparation of polymer nanoribbons

[0044] Dissolve 1.06 grams of p-xylene in 100 mL of nitrobenzene, add 13.4 grams of anhydrous aluminum trichloride, stir evenly, add 2.0 grams of dichloromethane, stir and react for 2 hours, and then transfer to a polytetrafluoroethylene reactor. Raise the temperature to 100°C to react for 12 hours, naturally cool, filter, wash with ethanol, and dry to obtain a brown-black spongy powder.

[0045] The chemical equation of this reaction is as follows (other embodiments are similar):

[0046]

[0047] (2) Calculation of nanoribbon strength

[0048] Using the molecular dynamics method, using MOPAC (2012 version) to simulate the stretching of the above-mentioned ladder molecular chain, the elastic modulus of the molecular chain is calculated to be as high as 550 GPa, figure 1 It is a scanning electron micrograph of the polymer nanobelt obtained in Example 1.

Embodiment 2

[0050] (1) Preparation of polymer nanoribbons

[0051] Dissolve 1.34 grams of p-diethylbenzene in 100 mL of nitrobenzene, add 6.4 grams of boron trifluoride, stir evenly, add 2.0 grams of dichloromethane, stir and react for 2 hours, then transfer to a polytetrafluoroethylene reactor, React at 100°C for 12 hours, filter after natural cooling, wash with ethanol, and dry to obtain a brown-black spongy powder.

[0052] (2) Calculation of nanoribbon strength

[0053] Using the molecular dynamics method and using MOPAC (2012 version) to simulate the stretching of the above-mentioned ladder molecular chain, the elastic modulus of the molecular chain is calculated to be as high as 431 GPa.

Embodiment 3

[0055] (1) Preparation of polymer nanoribbons

[0056] Dissolve 1.10 grams of hydroquinone in 100 mL of water, add 10 grams of concentrated sulfuric acid, stir well, add 2.0 grams of dichloromethane, stir well, then transfer to a polytetrafluoroethylene reactor, react at 190 ° C for 12 hours, after natural cooling Filter, wash with ethanol, and dry to obtain brown-black spongy powder.

[0057] (2) Calculation of nanoribbon strength

[0058] Using the molecular dynamics method and using MOPAC (2012 version) to simulate the stretching of the above-mentioned ladder molecular chain, the elastic modulus of the molecular chain is calculated to be as high as 570 GPa.

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Abstract

The invention provides high-strength polymer nanoribbons and a preparation method thereof. The nanoribbons are spontaneously generated in a polycondensation forming process of a polymer, wherein the polymer has the structure general formula as described in the specification, wherein R represents NH2, OH, alkoxy or alkyl, alkoxy is selected from methoxyl and ethyoxyl, and alkyl is selected from methyl or ethyl. The whole-carbon ladder polymer is formed by polycondensation of two monomers and spontaneously generates the nanoribbons during the forming process, no template agent and no subsequent processing are required, and a new technical idea and a new solving method are provided for synthesis of the high-strength nanoribbons; and the prepared polymer nanoribbons have high strength and excellent mechanical properties, and can be well used as reinforcing materials in composite materials.

Description

technical field [0001] The invention relates to the technical field of preparation of nanobelts, in particular to a high-strength polymer nanobelt and a preparation method thereof. Background technique [0002] At present, the shapes used as reinforcement materials in composite materials are usually fibers, nanowires, nanotubes, nanoribbons, and nanosheets, among which the fibers are prepared by spinning, while the reinforcement of the other four shapes Materials are prepared in a variety of ways, but overall they are complex. Except for a few polymers with low melting points that can be spun by dry spinning, most polymers can only be spun by wet spinning, which requires a large amount of solvents, which increases the cost of raw materials on the one hand, and increases the cost of the process on the other hand. The synthesis of nanowires and nanotubes generally adopts high-temperature chemical vapor deposition, which has complex processes and low yields. [0003] There ar...

Claims

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Application Information

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IPC IPC(8): C08G61/02C08G12/08C08G16/00C08G16/02
Inventor 曾绍忠王秀田赵志刚陈效华
Owner CHERY AUTOMOBILE CO LTD
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