Supported binary metal oxide nano-catalyst and preparation method thereof
A nano-catalyst and binary metal technology, applied in the field of nano-materials, can solve the problems of difficult large-scale promotion and application, high price, etc., and achieve the effect of cheap raw materials, less demand, and good thermal stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0032] 1. Ti 0.5 sn 0.5 o 2 Preparation of composite oxides: TiCl 4 solution and SnCl 4 ·5H 2 O was mixed according to the Ti:Sn molar ratio of 1:1, and the mixed solution was stirred for 1 hour, then slowly and uniformly added dilute ammonia water to the mixed solution while stirring until the pH=10, and the precipitation was complete. Then the resulting precipitate was washed with dilute ammonia water and suction filtered, then dried in an oven at 110°C for 12 hours, and ground; then roasted in a muffle furnace at 550°C for 4 hours to obtain Ti 0.5 sn 0.5 o 2 Composite oxides, spare.
[0033] 2. 6% Fe 2 o 3 / Ti 0.5 sn 0.5 o 2 Preparation of nanocatalyst: 1g Ti 0.5 sn 0.5 o 2 Put the composite oxide as a carrier into 7.04ml, 0.1mol L -1 Fe(NO 3 ) 3 Ultrasonic immersion in the solution for 2 hours, the ultrasonic frequency is 2000 Hz; then use 120 ° C oil bath to stir and evaporate the water; vacuum dry at 90 ~ 100 ° C for 10 hours, the vacuum degree is 400 P...
Embodiment 2
[0036] 1. Ti 0.5 sn 0.5 o 2 Preparation of composite oxides: TiCl 4 solution and SnCl 4 ·5H 2 O was mixed according to the Ti:Sn molar ratio of 1:1, and the mixed solution was stirred for 2 hours. Then, while stirring, dilute ammonia water was slowly and uniformly dropped into the mixed solution until the pH=10, and the precipitation was complete. Then the resulting precipitate was washed with dilute ammonia water and suction filtered, then dried in an oven at 120°C for 16 hours, and ground; then roasted in a muffle furnace at 550°C for 5 hours to obtain Ti 0.5 sn 0.5 o 2 Composite oxides, spare.
[0037] 2. 6% Fe 2 o 3 / 1%CeO 2 / Ti 0.5 sn 0.5 o 2 The preparation of binary metal oxide nano-catalyst comprises the following steps:
[0038] (1) Put 1g Ti 0.5 sn 0.5 o 2 Put the composite oxide as a carrier into 0.88ml0.1mol L -1 Ce(NO 3 ) 3 Ultrasonic immersion in the solution for 1.5h, the ultrasonic frequency is 2000Hz; then use a 120°C oil bath to stir and e...
Embodiment 3
[0042] 1. Ti 0.5 sn 0.5 o 2 The preparation of composite oxide is the same as in Example 1.
[0043] 2. 6% Fe 2 o 3 / 3%CeO 2 / Ti 0.5 sn 0.5 o 2 The preparation of binary metal oxide nano-catalyst comprises the following steps:
[0044] (1) Put 1g Ti 0.5 sn 0.5 o 2Put the composite oxide as a carrier into 2.64ml0.1mol L -1 Ce(NO 3 ) 3 Ultrasonic immersion in the solution for 1.5h, the ultrasonic frequency is 2000Hz; then use a 120°C oil bath to stir and evaporate to dryness; vacuum dry at 90-100°C for 10h, the vacuum degree is 400Pa; grind through a 160-mesh sieve. Calcined at 500°C for 4h in air atmosphere to get 3%CeO 2 / Ti 0.5 sn 0.5 o 2 Nano catalyst;
[0045] (2) The 3%CeO obtained in step (1) 2 / Ti 0.5 sn 0.5 o 2 Put the nano catalyst into 7.04ml0.1mol L -1 Fe(NO 3 ) 3 Ultrasonic immersion in the solution for 2 hours, the ultrasonic frequency is 2000 Hz; then use 120 ° C oil bath to stir and evaporate the water; vacuum dry at 90 ~ 100 ° C for 10 ...
PUM
Property | Measurement | Unit |
---|---|---|
Aperture | 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