Catalyst for preparing dichlorosilane, preparation method of catalyst and preparation method of dichlorosilane
A technology for silicon dichlorosilane and a catalyst is applied to the catalyst for preparing silicon hydrogen chloride and the field of preparation thereof, which can solve the problems of easy falling off, poor adsorption effect, low catalytic efficiency of the catalyst, etc., so as to improve the catalytic activity and increase the degree of dispersion. , the effect of reducing particle size
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0044] 1. Pretreatment of activated carbon: Take 30g of activated carbon, wash it with deionized water several times until the water after washing is clear, dry it naturally, and bake it in a blast oven at 110°C for 8 hours to obtain activated carbon CA1-0;
[0045] 2. Soak the activated carbon in 200ml of 1.0mol / L citric acid aqueous solution for 10 hours, take it out after soaking, and bake it in a blast oven at 110°C for 8 hours to obtain activated carbon CA1-1;
[0046] 3. Impregnate cobalt salt: A. Prepare 0.1mol / L CoCl 2 ·6H 2 O solution 500ml, B, get 20g activated carbon CA1-1, get 240ml CoCl prepared above 2 ·6H 2 O solution in a 500ml beaker, put activated carbon CA1-1 into CoCl 2 ·In the 6H2O solution, let it stand for immersion for 8 hours. C. After the immersion, remove the excess immersion liquid, dry it naturally, and dry it in a blast oven at 120°C for 10 hours to obtain activated carbon CA1-2;
[0047] 4. Roasting: Calcining activated carbon CA1-2 at a temp...
Embodiment 2
[0051] 1. Pretreatment of activated carbon: Take 30g of activated carbon, wash it with deionized water several times until the water after washing is clear, dry it naturally, and bake it in a blast oven at 100°C for 8 hours to obtain activated carbon CA2-0;
[0052] 2. Soak the activated carbon in 300ml of 1.2mol / L citric acid aqueous solution for 8 hours, take it out after soaking, and bake it in a blast oven at 100°C for 8 hours to obtain activated carbon CA2-1;
[0053] 3. Impregnate cobalt salt: A. Prepare 0.9mol / L CoCl 2 ·6H 2O solution 500ml, B, get 20g activated carbon CA2-1, get 300ml CoCl prepared above 2 ·6H 2 O solution in a 500ml beaker, put activated carbon CA2-1 into CoCl 2 ·6H 2 In the O solution, stand and soak for 20 hours. C. After the soaking is completed, remove the excess soaking liquid, dry it naturally, and dry it in a blast oven at 100°C for 8 hours to obtain activated carbon CA2-2;
[0054] 4. Roasting: Calcining activated carbon CA2-2 at a temper...
Embodiment 3
[0058] 1. Pretreatment of activated carbon: take 30g of activated carbon, wash it with deionized water several times until the rinsed water is clear, dry it naturally, and bake it in a blast oven at 120°C for 5 hours to obtain activated carbon CA3-0;
[0059] 2. Soak the activated carbon in 200ml of 0.4mol / L citric acid aqueous solution for 12 hours, take it out after soaking and dry it in a blast oven at 120°C for 5 hours to obtain activated carbon CA3-1;
[0060] 3. Impregnate cobalt salt: A. Prepare 0.5mol / L CoCl 2 ·6H 2 O solution 500ml, B, get 20g activated carbon CA3-1, get 300ml CoCl prepared above 2 ·6H 2 O solution in a 500ml beaker, put activated carbon CA3-1 into CoCl 2 ·6H 2 In the O solution, stand for immersion for 36 hours. C. After the immersion, remove the excess immersion liquid, dry it naturally, and dry it in a blast oven at 120°C for 5 hours to obtain activated carbon CA3-2;
[0061] 4. Roasting: Calcining activated carbon CA3-2 at a temperature of 32...
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