Preparation method and application of a high-efficiency photocatalyst srtio3/bi2wo6
A technology of photocatalysts and photocatalytic materials, applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxides/metal hydroxide catalysts, etc., can solve the problem of raw materials not being cheap, and achieve the goal of being green and environmentally friendly Secondary pollution, no secondary pollution, good catalytic activity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0019] The invention provides a high-efficiency photocatalytic material SrTiO 3 / Bi 2 WO 6 The preparation method, described photocatalyst is SrTiO 3 and Bi 2 WO 6 is a heterojunction catalyst formed by a secondary hydrothermal method, and the Bi 2 WO 6 It is a lamellar nanoparticle, and the preparation method comprises the following steps:
[0020] Step 1: Add TiCl 4 and Sr(OH) 2 ·8H 2 O was dissolved in a molar ratio of 1-5:1-10, then 11-15mL of 5mol / L NaOH solution was added dropwise, stirred evenly, placed in a hydrothermal kettle, heated at 120-180°C for 24-48h, and cooled to At room temperature, wash with deionized water and dry in vacuum to obtain nanoscale SrTiO 3 powder;
[0021] Step 2: To prepare different mass fractions of SrTiO 3 photocatalytic material, the prepared SrTiO 3 Powder, bismuth salt and tungstate are dissolved in deionized water according to the molar ratio of 1-10:0.5-15, SrTiO 3 The mass fraction is 1-15%, transferred to a hydrothermal...
Embodiment 1
[0028] 1.1 mL of TiCl 4 and 2.68g of Sr(OH) 2 ·8H 2 Dissolve O in 40mL of deionized water, add 13mL of 5mol / L NaOH solution dropwise, stir and transfer to a hydrothermal kettle, heat at 150°C for 36h, cool to room temperature after the reaction, wash with deionized water, and After vacuum drying at ℃ for 3h, SrTiO can be obtained 3 Powder; Weigh 0.1635g SrTiO 3 Dissolve in 40mL deionized water, add 4.8853g Bi(NO 3 ) 3 ·5H 2 O continued to stir, and 1.6621g Na 2 WO 4 2H 2 O was dissolved in 20mL deionized water, then added dropwise to the above precursor liquid, then transferred to a hydrothermal kettle, heated at 180°C for 12h; after the reaction was completed, cooled to room temperature, washed with deionized water, and dried in vacuum at 80°C The product can be obtained. 0.2g of SrTiO 3 / Bi 2 WO 6 The catalyst was dispersed into a 30 mg / L methyl orange solution, stirred vigorously for 30 min, and then irradiated by a visible light xenon lamp for 90 min. The abso...
Embodiment 2
[0030] 2.0 mL of TiCl 4 and 2.71g of Sr(OH) 2 ·8H 2 O was dissolved in 40mL of deionized water, and 14mL of 5mol / L NaOH solution was added dropwise, stirred, transferred to a hydrothermal kettle, heated at 160°C for 48h, cooled to room temperature after the reaction, washed with deionized water, and Vacuum drying at 80°C for 3 hours to obtain SrTiO 3 Powder; Weigh 0.1063g SrTiO 3 Dissolve in 40mL deionized water, add 4.9133g Bi(NO 3 ) 3 ·5H 2 O continued to stir, and 1.6592g (NH 4 ) 10 W 12 o 41 ·5H 2 After O was dissolved in 20mL of deionized water, it was added dropwise to the above precursor liquid, then transferred to a hydrothermal kettle, and heated at 180°C for 20h; after the reaction was completed, it was cooled to room temperature, washed with deionized water, and The product can be obtained by vacuum drying for 3 h. 0.2g of SrTiO 3 / Bi 2 WO 6 The catalyst was dispersed into a 30 mg / L rhodamine B solution, stirred vigorously for 30 min, and then irradia...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More - R&D
- Intellectual Property
- Life Sciences
- Materials
- Tech Scout
- Unparalleled Data Quality
- Higher Quality Content
- 60% Fewer Hallucinations
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2025 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com