Method for stripping Bi3O4Cl by using cell disintegrator and application of method in aspect of photocatalytic reduction of CO2
A pulverizer, photocatalytic technology, applied in catalyst activation/preparation, physical/chemical process catalyst, carbon monoxide, etc., can solve the problem of low photocatalytic efficiency, achieve high separation efficiency, fast migration rate, good photocatalytic reduction of CO2 performance effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] The present invention uses a cell pulverizer to peel off Bi 3 o 4 The method embodiment 1 of Cl, its method step is:
[0022] ⑴. Weigh 1 g Bi(NO 3 ) 3 ·5H 2O was fully stirred and dissolved in 35 ml of deionized water, then 0.5 g of tetracycline hydrochloride was added, stirred for 30 min, the mixture was transferred to a 40 ml polytetrafluoroethylene-lined stainless steel kettle, and reacted at 160 °C for 16 h. The samples after the hydrothermal reaction were taken out and centrifuged at 10,000 r / min for 10 min each time using a centrifuge. The centrifuged precipitate was washed several times with distilled water and ethanol, and finally dried in an oven at 80 °C for 24 h to obtain a black Bi-O-Cl complex precursor. Weigh 0.2 g of the dried precursor and put it into a muffle furnace for sintering at 550 °C for 3 h at a heating rate of 5 °C / min. After cooling down to room temperature naturally, collect the sample to obtain the bulk Bi 3 o 4 Cl photocatalyst;
[...
Embodiment 2
[0024] The present invention uses a cell pulverizer to peel off Bi 3 o 4 The method embodiment 2 of Cl, its method step is:
[0025] ⑴. Weigh 0.8 g Bi(NO 3 ) 3 ·5H 2 O was fully stirred and dissolved in 33 ml of deionized water, then 0.35 g of tetracycline hydrochloride was added, stirred for 40 min, the mixture was transferred to a 40 ml polytetrafluoroethylene-lined stainless steel kettle, and reacted at 180 °C for 16 h. The samples after the hydrothermal reaction were taken out and centrifuged at 10,000 r / min for 8 min each time using a centrifuge, and the centrifuged precipitates were washed several times with distilled water and ethanol respectively, and finally dried in an oven at 60 °C for 18 h to obtain black Bi- O-Cl complex precursor. Weigh 0.2 g of the dried precursor and put it into a muffle furnace for sintering at 500 °C for 5 h at a heating rate of 2 °C / min, and collect the sample after naturally cooling down to room temperature to obtain the bulk Bi 3 o ...
Embodiment 3
[0027] The present invention uses a cell pulverizer to peel off Bi 3 o 4 The method embodiment 3 of Cl, its method step is:
[0028] ⑴. Weigh 0.5 g Bi(NO 3 ) 3 ·5H 2 O was fully stirred and dissolved in 33 ml of deionized water, then 0.28 g of tetracycline hydrochloride was added, stirred for 30 min, the mixture was transferred to a 40 ml polytetrafluoroethylene-lined stainless steel kettle, and reacted at 180 °C for 24 h. The samples after the hydrothermal reaction were taken out and centrifuged at 10,000 r / min for 8 min each time using a centrifuge, and the centrifuged precipitates were washed several times with distilled water and ethanol respectively, and finally dried in an oven at 60 °C for 18 h to obtain black Bi- O-Cl complex precursor. Weigh 0.2 g of the dried precursor into a muffle furnace and sinter at 450 °C for 5 h with a heating rate of 1 °C / min, and collect samples after naturally cooling down to room temperature to obtain the bulk Bi 3 o 4 Cl photocatal...
PUM
Property | Measurement | Unit |
---|---|---|
water content | aaaaa | aaaaa |
thickness | aaaaa | aaaaa |
thickness | 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