Preparation of Mn-base metal oxide catalyst through H2O2 quick reduction method and application of Mn-base metal oxide catalyst to volatile organic chemicals (VOCs) low-temperature catalytic combustion
A low-temperature catalysis, H2O2 technology, applied in the direction of metal/metal oxide/metal hydroxide catalyst, physical/chemical process catalyst, catalyst activation/preparation, etc., can solve high hydrothermal temperature, waste water and residue, long reaction cycle etc. to achieve high catalytic activity, good adsorption, and large specific surface area
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0028] (1) Add 2 g of KMnO 4 and 0.8 g of 98% H 2 SO 4 Dissolved in 100 mL of deionized water to form a deep purple aqueous solution 1, in which KMnO 4 The concentration is about 0.02 g / mL;
[0029] (2) Mix 2 mL of analytically pure (30%) H 2 o 2 Dilute to solution 2 with 100 mL deionized water;
[0030] (3) At room temperature with rapid stirring, solution 2 was added dropwise to solution 1 to form a large amount of precipitate accompanied by a large amount of O 2 generate;
[0031] (4) Leave the precipitate to age overnight, filter and wash with water for 3-5 times;
[0032] (5) at 110 o C drying overnight, roasting in air to 400 o C and keep for 2 h, you can get MnO x catalyst powder;
[0033] (6) Characterized by scanning electron microscopy, the MnO synthesized in Example 1 x Amorphous solid particles on the microscopic scale, see figure 2 ;Characterized as α-MnO by XRD 2 ; via N 2 Static adsorption and desorption characterization, and the BET method was u...
Embodiment 2
[0036] (1) Add 3 g of KMnO 4 and 0.8 g of 98% H 2 SO 4 Dissolved in 100 mL of deionized water to form a deep purple aqueous solution 1, in which KMnO 4 The concentration is about 0.03 g / mL;
[0037] (2) Mix 8 mL of analytically pure (30%) H 2 o 2 Dilute to solution 2 with 100 mL deionized water;
[0038](3) At room temperature with rapid stirring, solution 2 was added dropwise to solution 1 to form a large amount of precipitate accompanied by a large amount of O 2 generate;
[0039] (4) Leave the precipitate to age overnight, filter and wash with water for 3-5 times;
[0040] (5) at 110 o C drying overnight, roasting in air to 400 o C and keep for 2 h, you can get MnO x catalyst powder;
[0041] (6) Characterized by scanning electron microscopy, the MnO synthesized in Example 2 x Hierarchical structures formed for rod-like and granular packing on the microscopic scale, see image 3 ; Characterized as amorphous MnO by XRD 2 ; via N 2 Characterized by static adsor...
Embodiment 3
[0046] (1) Add 3 g of KMnO 4 and 0.5 g of 95% H 3 PO 4 Dissolved in 100 mL of deionized water to form a deep purple aqueous solution 1, in which KMnO 4 The concentration is about 0.02 g / mL;
[0047] (2) Mix 8 mL of analytically pure (30%) H 2 o 2 Dilute to solution 2 with 100 mL deionized water;
[0048] (3) At room temperature with rapid stirring, solution 2 was added dropwise to solution 1 to form a large amount of precipitate accompanied by a large amount of O 2 generate;
[0049] (4) Leave the precipitate to age overnight, filter and wash with water for 3-5 times;
[0050] (5) at 110 o C drying overnight, roasting in air to 400 o C and keep for 2 h, you can get MnO x catalyst powder;
[0051] (6) The catalyst is characterized by XRD as amorphous MnO 2 ;
[0052] (7) In the fixed-bed reactor, evaluate the catalytic combustion performance of high-concentration toluene, the catalyst dosage is 0.2 g, and the catalyst is 40-60 mesh solid particles after sieving, th...
PUM
Property | Measurement | Unit |
---|---|---|
Specific surface area | 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