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Method for preparing degradable biocompatibility macromolecule/carbon nano-tube composite material

A technology of biocompatibility and carbon nanotubes, applied in the field of biomedical materials, can solve problems such as difficulty in uniform dispersion, affecting the enhancement effect and function of carbon nanotubes, and achieve convenient operation, adsorption, cell affinity and biological Good degradability and the effect of solving the problem of agglomeration

Inactive Publication Date: 2010-12-08
UNIV OF SCI & TECH BEIJING
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] Due to the large specific surface area and strong interaction of carbon nanotubes, it is very easy to spontaneously form rods with a diameter of 10-100nm. It is difficult to disperse uniformly, but exists in agglomerated state with large size, which affects the reinforcing effect and function of carbon nanotubes in the polymer matrix, as well as the forming and processing performance of polymer / carbon nanotube composites
None of the existing chemical modification and purification technologies can effectively solve this problem

Method used

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  • Method for preparing degradable biocompatibility macromolecule/carbon nano-tube composite material
  • Method for preparing degradable biocompatibility macromolecule/carbon nano-tube composite material

Examples

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example 1

[0021] Add carbon nanotubes (multi-walled carbon nanotubes, inner diameter 80-100nm, length 1-2μm) into concentrated sulfuric acid at 3g / L, stir and reflux for 4 hours at 80°C, and continue to reflux for 1 hour at room temperature. Deionized water was added to the resulting solution and centrifuged to remove the acid remaining in the solution until the solution was substantially neutral. The solution was then dried for 12 hours to fully remove residual moisture. The obtained carbon nanotube powder was ground for 15 minutes to obtain acidified carbon nanotubes. Dissolve 1.5g of PHBV (containing 79% of PHV) in 60ml of chloroform, and reflux in a 50°C water bath until fully dissolved. Add 0.0045 g of carbon nanotubes treated with surfactant, and disperse by ultrasonic for 10 min. After the mold is preheated at a temperature of 40° C., the dispersed solution is poured into a petri dish and left to stand for 2 minutes. First evaporate a large amount of solvent under the conditio...

example 2

[0023] At room temperature, prepare an aqueous solution of polyvinylpyrrolidone with a concentration of 0.002g / mL, and dissolve in a water bath at 40°C. Add 0.7 g of carbon nanotubes (multi-walled carbon nanotubes, with an inner diameter of 40-60 nm and a length of 5-15 μm), and ultrasonically disperse for 15 min. The mixture was centrifuged, the water layer was removed, and placed in a vacuum oven. After fully drying to constant weight, grinding is carried out to obtain surface-activated carbon nanotubes. Dissolve 1.5g of polylactic acid in 60ml of acetone, and bathe in water at 40°C until fully dissolved. Add 0.0075 g of carbon nanotubes treated with surfactant, and disperse by ultrasonic for 10 min. After the mold is preheated at a temperature of 30°C, the dispersed solution is poured into a petri dish and left to stand for 3 minutes. A large amount of solvent is evaporated at 5°C, and then dried at room temperature for molding.

example 3

[0025]Add carbon nanotubes (single-wall carbon nanotubes, inner diameter ≤ 2nm, length 1-2μm) into concentrated nitric acid solution at 3.5g / L, stir and reflux for 3.5 hours at 90°C, and continue to reflux for 2 hours at room temperature. Deionized water was added to the resulting solution and centrifuged to remove the acid remaining in the solution until the solution was substantially neutral. The solution was then dried for 12 hours to fully remove residual moisture. The obtained carbon nanotube powder was ground for 15 minutes to obtain acidified carbon nanotubes. Dissolve 1.5g of polycaprolactate in 60ml of xylene, and reflux in a water bath at 60°C until fully dissolved. Add 0.0075 g of carbon nanotubes treated with surfactant, and disperse by ultrasonic for 10 min. After the mold is preheated at a temperature of 50° C., the dispersed solution is poured into a petri dish and left to stand for 2 minutes. Dry and shape at room temperature.

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Abstract

The invention provides a preparation process of degradable biocompatible macromolecule / carbon nano pipe composite material, relating to the preparation of biocompatible degradable macromolecule / carbon nano pipe composite material which has high strength and high toughness. The invention adopts the technique of conducting surface activating, multiple phase solution dispersion, casing formation and heating processing for the carbon nano pipe with carboxylation and surface activator to prepare biological medical degradable polymer or carbon nano pipe composite material, which reduces the aggregation and entanglement phenomenon of the carbon nano pipe in solution, solves the problem of aggregating of the carbon nano pipe in macromolecules, forms firm interface interacting action with the polymer, thereby obviously increasing the mechanical property of degradable macromolecule. The carbon nano pipe / degradable macromolecule composite material with different dimension and shape which has high strength and high toughness can be obtained, in particular to reinforced polymer composite material of acidulating carbon nano pipe, wherein the tension strength is increased over 6.50 MPa, elasticity modulus is increased over 250 MPa, which has excellent surface wettability, adsorbability to protein and biomolecule, cellular affinity and biological degradation.

Description

technical field [0001] The invention relates to the field of biomedical materials, in particular to the preparation of high-strength and high-toughness biocompatible degradable polymer / carbon nanotube composite materials. Background technique [0002] Carbon nanotubes are closed nanotubes formed by bending single-layer or multi-layer six-membered carbon ring graphite layers. Both ends of the tube are hemispherically capped like half a fullerene molecule, and the aspect ratio is generally greater than 1000. . The unique structure of this new quasi-one-dimensional functional material makes it have excellent mechanical, electrical and thermal properties. The carbon-carbon bonds and closed structure of carbon nanotubes perfectly arranged in the axial direction lead to extremely high axial strength and elastic modulus. For example, the tensile strength of carbon nanotubes is about 100-600GPa, which is higher than that of existing high-strength carbon fibers. Two orders of magni...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08L67/04C08K9/04C08L77/00C08L85/02C08K3/04
Inventor 郑裕东魏广叶姚学锋刘国权
Owner UNIV OF SCI & TECH BEIJING