Acetylene process vinyl acetate catalyst
A vinyl acetate and catalyst technology, which is applied in the field of acetylene vapor phase vinyl acetate catalyst, can solve the problems of low benzene content of by-products and high content of by-product benzene, and achieve the effects of reducing benzene content, improving selectivity, and good technical effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0029] (1) Catalyst preparation
[0030] (a) Impregnation: take Fe(NO 3 ) 3 100ml of aqueous solution is impregnation solution A (Fe 3+ Concentration: 2.0g / L), impregnate 100ml of coal-based columnar carbon with a diameter of 2.4mm and a length of 2cm at a room temperature of 25°C (BET specific surface 1200cm 2 / g, the total adsorption pore volume is 0.7cm 3 / g) 3h;
[0031] (b) drying: after drying in a vacuum oven at 90° C. for 4 hours, the carrier precursor is obtained;
[0032] (c) reduction: in H 2 / N 2 Mixed gas (H 2 Molar concentration is 10%) after reduction at 200°C for 1h, in N 2 Cool to room temperature in the atmosphere to obtain a modified activated carbon carrier;
[0033] (d) Preparation of immersion solution: Weigh 18.0g of zinc acetate (molecular formula: Zn(CH 3 COO) 2 ) solid was dissolved in pure water at 60°C to prepare 180ml of impregnating liquid, and acetic acid was used to adjust the pH value of the impregnating liquid to 4.85 to obtain impr...
Embodiment 2
[0048] (1) Catalyst preparation
[0049] (a) Impregnation: take CoCl-containing 2 100ml of aqueous solution is impregnation solution A (Co 2+ Concentration: 2.0g / L), impregnate 100ml of coal-based columnar carbon with a diameter of 2.4mm and a length of 2cm at a room temperature of 25°C (BET specific surface 1200cm 2 / g, the total adsorption pore volume is 0.7cm 3 / g) 3h;
[0050] (b) drying: after drying in a vacuum oven at 90° C. for 4 hours, the carrier precursor is obtained;
[0051] (c) reduction: in H 2 / N 2 Mixed gas (H 2 Molar concentration is 10%) after reduction at 200°C for 1h, in N 2 Cool to room temperature in the atmosphere to obtain a modified activated carbon carrier;
[0052] (d) Preparation of immersion solution: Weigh 18.0g of zinc acetate (molecular formula: Zn(CH 3 COO) 2 ) solid was dissolved in pure water at 60°C to prepare 180ml of impregnating liquid, and acetic acid was used to adjust the pH value of the impregnating liquid to 4.85 to obtain...
Embodiment 3
[0059] (1) Catalyst preparation
[0060] (a) Impregnation: take Ni(NO 3 ) 2 100ml of aqueous solution is impregnation solution A (Ni 2+ Concentration: 2.0g / L), impregnate 100ml of coal-based columnar carbon with a diameter of 2.4mm and a length of 2cm at a room temperature of 25°C (BET specific surface 1200cm 2 / g, the total adsorption pore volume is 0.7cm 3 / g) 3h;
[0061] (b) drying: after drying in a vacuum oven at 90° C. for 4 hours, the carrier precursor is obtained;
[0062] (c) reduction: in H 2 / N 2 Mixed gas (H 2 Molar concentration is 10%) after reduction at 200°C for 1h, in N 2 Cool to room temperature in the atmosphere to obtain a modified activated carbon carrier;
[0063] (d) Preparation of immersion solution: Weigh 18.0g of zinc acetate (molecular formula: Zn(CH 3 COO) 2 ) solid was dissolved in pure water at 60°C to prepare 180ml of impregnating liquid, and acetic acid was used to adjust the pH value of the impregnating liquid to 4.85 to obtain impr...
PUM
Property | Measurement | Unit |
---|---|---|
Diameter | aaaaa | aaaaa |
Adsorption total pore volume | aaaaa | aaaaa |
Specific surface | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
![application no application](https://static-eureka.patsnap.com/ssr/23.2.0/_nuxt/application.06fe782c.png)
- 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