Co-doped bismuth phosphate-base composite photocatalytic material and preparation method thereof
A composite photocatalysis and bismuth phosphate technology, applied in chemical instruments and methods, physical/chemical process catalysts, chemical/physical processes, etc., can solve the problems of low utilization of sunlight and large forbidden band width, etc., to improve photocatalysis Activity, improve absorption properties, enhance the effect of migration efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0023] The preparation method of the above-mentioned co-doped bismuth phosphate-based composite photocatalytic material specifically comprises the following steps:
[0024] Step 1: Dissolving bismuth nitrate pentahydrate in nitric acid solution with a mass concentration of 65% to obtain solution A, wherein the mass ratio of bismuth nitrate pentahydrate and nitric acid is 1:5-10; phosphate, ammonium tungstate and vanadium Ammonium acid is dissolved in a sodium hydroxide solution with a concentration of 1-2mol / L to obtain a solution B, wherein the molar ratio of phosphate ions, tungstate ions, vanadate ions and sodium hydroxide is 1:0.1-0.3:0.1-0.3 : 1 ~ 4; Mix solution A and solution B evenly to obtain solution C, wherein the molar ratio of phosphate ion, tungstate ion, vanadate ion and bismuth ion in solution C is 1: 0.1 ~ 0.3: 0.1 ~ 0.3: 1.3 ~1.9; transfer solution C to a hydrothermal reaction kettle, and place it in a microwave reactor and heat it to 150~250°C for 1~3h with ...
Embodiment 1
[0029] Step 1: Dissolving 6.31g bismuth nitrate pentahydrate in 31.55g mass concentration is 65% nitric acid solution to obtain solution A. Dissolve 1.64g sodium phosphate, 3.04g ammonium tungstate and 0.12g ammonium metavanadate in 20ml, concentration It is a 1mol / L sodium hydroxide solution to obtain solution B; mix solution A and solution B evenly to obtain solution C; transfer solution C to a hydrothermal reaction kettle, and place it in a microwave reactor and heat it to 150°C by microwave Hydrothermal treatment for 1 hour, take it out and cool it to room temperature naturally, centrifuge the obtained product, wash with deionized water 3 times, and dry at 80°C for 12 hours to obtain a mixed powder of bismuth phosphate, bismuth tungstate and bismuth vanadate;
[0030] Step 2: Disperse 3.85g of the mixed powder obtained in step 1 in 65ml of ammonium fluoride solution with a concentration of 0.1mol / L, then transfer to a hydrothermal reaction kettle, and place it in a microwav...
Embodiment 2
[0033]Step 1: Dissolving 9.22g bismuth nitrate pentahydrate in 92.2g mass concentration of 65% nitric acid solution to obtain solution A, 1.64g sodium phosphate, 9.12g ammonium tungstate and 0.36g ammonium metavanadate were dissolved in 20ml, concentration 2mol / L sodium hydroxide solution to obtain solution B; mix solution A and solution B evenly to obtain solution C; transfer solution C to a hydrothermal reaction kettle, and place it in a microwave reactor and heat it to 250°C with microwaves After hydrothermal treatment for 3 hours, take it out and cool it down to room temperature naturally, centrifuge the obtained product, wash it with deionized water three times, and dry it at 80°C for 12 hours to obtain a mixed powder of bismuth phosphate, bismuth tungstate and bismuth vanadate;
[0034] Step 2: Disperse 3.85g of the mixed powder obtained in step 1 in 13ml of ammonium fluoride solution with a concentration of 1mol / L, then transfer it to a hydrothermal reaction kettle, and ...
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