Ultrahigh-molecular weight polyethylene composite material for artificial joint and preparation method of ultrahigh-molecular weight polyethylene composite material
An ultra-high molecular weight, artificial joint technology, applied in the field of ultra-high molecular weight polyethylene composite materials for artificial joints and their preparation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0019] A method for preparing an ultrahigh molecular weight polyethylene composite material for artificial joints of chimeric polymer macromolecular chains provided by the invention comprises the following steps:
[0020] 1. Put the ultra-high molecular weight polyethylene powder in a benzophenone (5-20mg / ml) solution and let it stand in the dark for 5-40 minutes, and then dry it in a vacuum in the dark. The ultra-high molecular weight polyethylene powder is medical grade. The molecular weight is above 1.5 million, and the diameter is 13-270 μm;
[0021] 2. Add ultra-high molecular weight polyethylene powder coated with a photosensitizer on the surface to the monomer solution to be grafted, stir evenly, and irradiate with ultraviolet light for 10-90 minutes. After the irradiation, the powder is washed and dried, wherein the monomer The body has good biocompatibility, and can be acrylic acid, 2-methacryloyloxyethyl phosphorylcholine (MPC), N-vinylpyrrolidone, acrylamide, ...
Embodiment 1
[0027]The ultra-high molecular weight polyethylene powder with a diameter of 270 μm was immersed in an acetone solution of benzophenone (10 mg / ml), allowed to stand for 5 min, and then dried in vacuum in the dark. Add the powder coated with the photosensitizer into the acrylamide monomer solution, place it on a magnetic stirrer and mix evenly, and irradiate with 500W ultraviolet light for 80 minutes in a nitrogen protective atmosphere to obtain superhigh Molecular weight polyethylene powder. The grafted powder material was washed with ethanol and dried in vacuum. Put the above powder material into the mold, under vacuum conditions (-0.1MPa), 190°C, hot pressing pressure 12MPa, heat preservation and pressure holding for 1.5h, cooling and demoulding to take out the sample.
[0028] A pin-on-disc friction tester was used to test the tribological properties. Under normal saline lubrication conditions, the friction coefficient of the samples decreased from 0.054 before grafting t...
Embodiment 2
[0030] The ultra-high molecular weight polyethylene powder with a diameter of 100 μm was immersed in a diethyl ether solution of benzophenone (5 mg / ml), allowed to stand for 20 min, and then dried under vacuum in the dark. Add the powder coated with the photosensitizer into the acrylic acid monomer solution, place it on a magnetic stirrer, stir and mix evenly, and irradiate with 500W ultraviolet light for 10 minutes in a nitrogen protective atmosphere to obtain an ultra-high molecular weight polymer grafted with acrylic acid macromolecular chains. vinyl powder. The grafted powder material was washed with ethanol and dried in vacuum. The above powder material and pure ultra-high molecular weight polyethylene block are layered into the mold, under vacuum conditions, 150 ° C, hot pressing pressure 7.5 MPa, heat preservation and pressure holding time 2.5 h. Cool and demould to take out the sample.
[0031] Using a pin-on-disk friction tester and a reciprocating friction tester, ...
PUM
Property | Measurement | Unit |
---|---|---|
concentration | aaaaa | aaaaa |
diameter | aaaaa | aaaaa |
wavelength | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com