A manganese-doped maghemite catalyst for thermocatalytic oxidation of formaldehyde and preparation method thereof
A technology of maghemite and manganese doping, which is applied in the field of manganese-doped maghemite catalyst and its preparation, can solve the problems of low catalytic activity, easy loss, high price, etc., and achieve high catalytic activity and light-off temperature Low, good thermal stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0018] 1. Weigh 27.8g FeSO 4 ·7H 2 O (0.1mol), 54.1g FeCl 3 ·6H 2 O (0.2mol) was added into 400mL ultrapure water (x=0), and under the protection of argon, it was completely dissolved to obtain 2+ , Fe 3+ solution of metal ions.
[0019] 2. Under the protection of argon, add the metal ion solution dropwise into 210mL of 4mol / L NaOH solution, and keep stirring the solution to form a black precipitate until the precipitation is complete; then crystallize the black precipitate at a constant temperature of 90°C for 24 hours .
[0020] 3. Centrifuge the black precipitate, collect the black precipitate, wash 3 times with ultrapure water, use a freeze dryer, freeze-dry in vacuum at a temperature of -40~-50°C for 24 hours, and obtain granular manganese-doped Magnetite precursor.
[0021] 4. Grading and screening Take the 35-60 mesh manganese-doped magnetite precursor, put it in a muffle furnace and roast it at 450° C. for 4 hours to obtain a composite sample 1 .
[0022] 5. Th...
Embodiment 2
[0024] 1. Weigh 22.2g FeSO 4 ·7H 2 O (0.08mol), 54.1g FeCl 3 ·6H 2 O (0.2mol), 3.4g MnSO 4 ·H 2 O (0.02mol) was added into 400mL ultrapure water (x=0.2), and under the protection of argon, it was completely dissolved to obtain 2+ , Fe 3 + , Mn 2+ solution of metal ions.
[0025] 2. Under the protection of argon, add the metal ion solution dropwise into 210mL of 4mol / L NaOH solution, and keep stirring the solution to form a black precipitate until the precipitation is complete; then crystallize the black precipitate at a constant temperature of 90°C for 24 hours .
[0026] 3. Centrifuge the black precipitate, collect the black precipitate, wash 3 times with ultrapure water, use a freeze dryer, and freeze-dry at a temperature of -40 to -50°C for 24 hours in a vacuum. After drying, granular manganese-doped magnetic Iron ore precursors.
[0027] 4. Grading and screening Take the 35-60 mesh manganese-doped magnetite precursor, put it in a muffle furnace and roast it at 4...
Embodiment 3
[0030] 1. Weigh 13.9g FeSO 4 ·7H 2 O (0.05mol), 54.1g FeCl 3 ·6H 2 O (0.2mol), 8.5g MnSO 4 ·H 2 O (0.05mol) was added into 400mL ultrapure water (x=0.5), and under the protection of argon, it was completely dissolved to obtain 2+ , Fe 3 + , Mn 2+ solution of metal ions.
[0031] 2. Under the protection of argon, add the metal ion solution dropwise into 210mL of 4mol / L NaOH solution, and keep stirring the solution to form a black precipitate until the precipitation is complete, and then crystallize the black precipitate at a constant temperature of 100°C for 24 hours .
[0032] 3. Centrifuge the black precipitate, collect the black precipitate, wash 3 times with ultrapure water, use a freeze dryer, and freeze-dry at a temperature of -40 to -50°C for 24 hours in a vacuum. After drying, granular manganese-doped magnetic Iron ore precursors.
[0033] 4. Grading and screening Take the 35-60 mesh manganese-doped magnetite precursor, put it in a muffle furnace and roast it a...
PUM
| Property | Measurement | Unit |
|---|---|---|
| clearance rate | aaaaa | aaaaa |
| clearance rate | aaaaa | aaaaa |
| clearance rate | aaaaa | aaaaa |
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


