Method for modifying carbon fibers by dendritic macromoleculars

A macromolecular, carbon fiber technology, applied in carbon fiber, fiber processing, textiles and papermaking, etc., can solve the problems of membrane limitation and poor stability, and achieve the effect of simple process, improved interface strength and unique rheological properties

Inactive Publication Date: 2010-05-19
HARBIN INST OF TECH
View PDF0 Cites 19 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The technical problem to be solved by the present invention is to solve the problem that only one functional group of the organosilicon compound can react with the modified surface of the fiber so that the film is limited to the two-dimensional surface and has poor stability. A method for modifying carbon fibers with dendrimers is provided.

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
  • Method for modifying carbon fibers by dendritic macromoleculars
  • Method for modifying carbon fibers by dendritic macromoleculars
  • Method for modifying carbon fibers by dendritic macromoleculars

Examples

Experimental program
Comparison scheme
Effect test

specific Embodiment approach 1

[0008] Embodiment 1: The method for modifying carbon fibers with dendrimers in this embodiment is as follows: 1. Add carbon fibers to a strong oxidizing acid to prepare a mixture, and then ultrasonically treat the mixture for 15 minutes to 60 minutes at a frequency of 10KHz to 100KHz , and then stir the mixture for 10min~20min, then heat to 60℃~100℃ and reflux for 2h~4h, then take out the carbon fiber and wash it with deionized water until the washing liquid is neutral, and then put the carbon fiber at 20℃~100℃, the vacuum degree is - Dry under the condition of 0.05MPa~-0.1MPa for 1h~3h to obtain acidified carbon fiber; 2. Dissolve the dendrimer in the solvent to obtain the dendrimer solution, and then add the acidified carbon fiber into the dendrimer solution , to obtain a mixed solution, then ultrasonically treat the mixed solution for 5min to 30min under the condition of 20KHz to 50KHz, and then react for 1h to 24h under the condition of 20°C to 100°C, and then alternately w...

specific Embodiment approach 2

[0013] Specific embodiment two: the difference between this embodiment and specific embodiment one is that the strong oxidizing acid described in step one is nitric acid with a mass concentration of 1% to 70%, sulfuric acid and permanganese with a mass concentration of 1% to 100%. Potassium permanganate sulfuric acid solution with potassium permanganate concentration of 1g / L~50g / L or nitric acid with mass concentration of 1%~70% and sulfuric acid with mass concentration of 1%~100% according to the volume ratio of 1~9:1. mixed acid. Others are the same as in the first embodiment.

[0014] The interfacial shear strength of the dendrimer-modified carbon fiber / epoxy resin composite material prepared by using the dendrimer-modified carbon fiber obtained in this embodiment is 53.2MPa-55.8MPa, which is higher than that of the ring prepared by using imported carbon fiber at the same level. The interface strength of the oxygen resin composite material is increased by 30% to 70%.

specific Embodiment approach 3

[0015] Embodiment 3: The difference between this embodiment and Embodiment 1 or 2 is that the dendrimers described in Step 2 are 1st to 4th generation hydroxyl-terminated dendrimers or 1st to 4th generation amino-terminated dendrimers. macromolecule. Others are the same as in the first or second embodiment.

[0016] The interfacial shear strength of the dendrimer-modified carbon fiber / epoxy resin composite material prepared by using the dendrimer-modified carbon fiber obtained in this embodiment is 53.2MPa-55.8MPa, which is higher than that of the ring prepared by using imported carbon fiber at the same level. The interface strength of the oxygen resin composite material is increased by 30% to 70%.

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
shear strengthaaaaaaaaaa
Login to view more

Abstract

The invention provides a method for modifying carbon fibers by dendritic macromoleculars, relating to a method for modifying the carbon fibers and aiming at solving the problem of poor stability due to that only one functional group of organic silicon compound can react with the fiber modified surface so as to limit a membrane in a bidimensional surface. The method comprises the following steps: adding carbon fibers in a strong oxidizing acid, utilizing ultrasonic for processing, heating and refluxing, drying, adding into dendritic macromolecular solution for ultrasonic processing once again, reacting under the temperature of 20-100 DEG C, washing and drying to obtain the carbon fibers modified by the dendritic macromoleculars. The dendritic macromoleculars used in the invention have the advantages of tri-dimensional structure, evenly-distributed and thick outer functional groups, lower viscosity, unique flowing deformation property, good film forming property and favorable modified effect. The epoxy resin composite material prepared by using the carbon fibers modified by the dendritic macromoleculars obtained in the invention has 53.2-55.8MPa of interface shearing strength.

Description

technical field [0001] The invention relates to a method for modifying carbon fibers. Background technique [0002] The most commonly used functional group modification of fibers is alkane chain organic molecules (such as silane coupling agents). This organosilicon compound, which has two different reactive groups in the molecule at the same time, can form a bonding layer of inorganic phase-silane coupling agent-organic phase, so that better adhesion can be obtained between the interface between the polymer and the inorganic material. connection strength. However, its significant defect is that the organosilicon compound usually has only one functional group that can react with the modified surface of the fiber, so there is only one binding point, so the film is limited to a two-dimensional surface and has poor stability. Contents of the invention [0003] The technical problem to be solved by the present invention is to solve the problem that only one functional group o...

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): D06M10/06D06M10/10D06M15/53D06M15/507D06M15/564D06M15/59D06M11/64D06M11/55D06M11/50C08L63/00C08L63/02C08K9/04C08K9/02C08K7/06D06M101/40
Inventor 赫晓东梅蕾李宜彬王荣国彭庆宇
Owner HARBIN INST OF TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap