Method for preparing molybdenum powder for preparing molybdenum end cap of magnetron
A molybdenum end cap and magnetron technology, which is applied in the field of metal powder manufacturing, can solve the problems of low atomization rate, low production efficiency, and low yield of atomizers, so as to avoid pollution and damage the environment, high production efficiency, The effect of high yield
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0023] The preparation method of the molybdenum powder for the preparation of the magnetron molybdenum end cap of the present embodiment is as follows:
[0024] Step 1. Stir polyvinyl alcohol and deionized water at a mass ratio of 1:100 for 34 minutes at a temperature of 86° C. to form a binder; the average degree of polymerization of the polyvinyl alcohol is 1300, and the degree of alcoholysis is 89 %;
[0025] Step 2, stirring the raw material molybdenum powder with the binder and the Fischer grain size of 3.5 μm and a mass purity of 99.9% in the step 1 at a temperature of 20° C. for 50 minutes to obtain a slurry; The mass fraction of ionized water is 20%;
[0026] Step 3. Put the slurry described in step 2 into a spray drying tower for granulation to obtain pellets; the temperature of the air inlet of the spray drying tower is 210°C, the temperature of the air outlet is 140°C, and the spray drying tower is atomized The rotational speed of the tor is 1.5 x 10 4 r / min, the...
Embodiment 2
[0030] The preparation method of the molybdenum powder for the preparation of the magnetron molybdenum end cap of the present embodiment is as follows:
[0031] Step 1. Stir polyvinyl alcohol and deionized water at a mass ratio of 1.3:100 at a temperature of 80°C for 50 minutes to form a binder; the average degree of polymerization of the polyvinyl alcohol is 2000, and the degree of alcoholysis is 90 %;
[0032] Step 2, stirring the raw material molybdenum powder with the binder and the Fischer particle size of 2.0 μm and a mass purity of 99.5% in step 1 at a temperature of 21° C. for 30 minutes to obtain a slurry; The mass fraction of ionized water is 25%;
[0033] Step 3. Put the slurry described in step 2 into a spray drying tower for granulation to obtain pellets; the air inlet temperature of the spray drying tower is 240°C, the air outlet temperature is 100°C, and the spray drying tower is atomized The rotational speed of the tor is 1.5 x 10 4 r / min, the atomization ra...
Embodiment 3
[0037] The preparation method of the molybdenum powder for the preparation of the magnetron molybdenum end cap of the present embodiment is as follows:
[0038] Step 1. Stir polyvinyl alcohol and deionized water at a mass ratio of 1.8:100 at a temperature of 95°C for 30 minutes to form a binder; the average degree of polymerization of the polyvinyl alcohol is 1800, and the degree of alcoholysis is 99 %;
[0039] Step 2, the binder described in step 1 and the Fibonacci particle size are 2.5 μ m, and the raw material molybdenum powder with a mass purity of 99.8% is stirred at a temperature of 22° C. for 40 minutes to obtain a slurry; The mass fraction of ionized water is 28%;
[0040] Step 3. Put the slurry described in step 2 into a spray drying tower to granulate to obtain pellets; the air inlet temperature of the spray drying tower is 200°C, the air outlet temperature is 130°C, and the spray drying tower is atomized The rotational speed of the tor is 1.9×10 4 r / min, the at...
PUM
Property | Measurement | Unit |
---|---|---|
particle size | aaaaa | aaaaa |
particle size | aaaaa | aaaaa |
particle size | 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