Preparation method of stable type compound nano anti-wearing agent
A nanometer anti-wear and stable technology, used in additives, lubricating compositions, petroleum industry and other directions, can solve the problems of difficulty in aggregation of molybdenum disulfide powder, increase molybdenum disulfide lipophilic performance, increase stability and uniformity, etc. , to achieve the effect of no nano-agglomeration, small amount of addition, and reduced friction and wear
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
example 1
[0017] First, 100g of nano-molybdenum disulfide and mass fraction of 15% n-butyllithium n-hexane solution are added to a three-necked flask with a thermometer and a reflux device at a mass ratio of 1:15, and the flask is placed in an oil bath, controlled The temperature was 95°C, magnetically stirred and reacted for 3 hours. After the reaction was completed, stop heating. After the temperature was naturally cooled to room temperature, nitrogen gas was passed into the product at a rate of 30 mL / min. After stirring for 24 hours, the nitrogen gas was stopped, and Move the product into a centrifuge, centrifuge at a speed of 4500r / min for 15min, collect the precipitate, and wash it twice with n-hexane to obtain pretreated molybdenum disulfide; then the above pretreated molybdenum disulfide, mercaptoethylamine and water are Add 1:2:5 into the beaker, place the beaker in an ultrasonic oscillator, disperse ultrasonically at 40KHz for 12h, then transfer to a centrifuge, centrifuge at 45...
example 2
[0020] First, 110g of nanomolybdenum disulfide and mass fraction of 15% n-butyllithium n-hexane solution are added to a three-necked flask with a thermometer and a reflux device at a mass ratio of 1:15, the flask is placed in an oil bath, and the control The temperature was 98°C, magnetically stirred and reacted for 3 hours. After the reaction was completed, stop heating. After the temperature was naturally cooled to room temperature, nitrogen gas was passed into the product at a rate of 35 mL / min. After stirring for 25 hours, the nitrogen gas was stopped, and Move the product into a centrifuge, centrifuge at a speed of 5000r / min for 20min, collect the precipitate, and wash it twice with n-hexane to obtain pretreated molybdenum disulfide; then the above pretreated molybdenum disulfide, mercaptoethylamine and water are Add 1:2:5 into the beaker, place the beaker in an ultrasonic oscillator, disperse ultrasonically at 45KHz for 13h, then transfer to a centrifuge, centrifuge at a ...
example 3
[0023] First, 120g of nanomolybdenum disulfide and mass fraction of 15% n-butyllithium n-hexane solution are added to a three-necked flask with a thermometer and a reflux device at a mass ratio of 1:15, the flask is placed in an oil bath, and the control The temperature was 100°C, magnetically stirred and reacted for 4 hours. After the reaction was completed, stop heating. After the temperature was naturally cooled to room temperature, nitrogen gas was passed into the product at a rate of 40 mL / min. After stirring for 26 hours, the nitrogen gas was stopped, and The product is moved into a centrifuge, centrifuged at a speed of 5000r / min for 20min, the precipitate is collected, and washed 3 times with n-hexane to obtain pretreated molybdenum disulfide; then the above pretreated molybdenum disulfide, mercaptoethylamine and water are Add 1:2:5 into the beaker, place the beaker in an ultrasonic oscillator, disperse ultrasonically at 50KHz for 14h, then transfer to a centrifuge, cent...
PUM
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