Olefin-alkane separating adsorbent and preparation method and application thereof
A technology for olefin alkane and adsorbent, which is applied in the field of adsorbent for olefin alkane separation and its preparation, and achieves the effects of simple method, improved adsorption and separation selectivity, and large adsorption capacity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0016] Preparation of porous carbon: Dissolve 1.0g of asphaltene in 20mL of benzene, take 1g of triblock copolymer F108 (EO 132 PO 50 EO 132 ) was dissolved in 20mL of benzene, benzene was removed in one step in an oven at 100°C and thermal polymerization was carried out, and finally under the protection of inert gas, the temperature was raised to 700°C to obtain porous carbon (specific surface area of 2500m 2 / g).
[0017] Preparation of adsorbent: Weigh 1 g of porous carbon and 1.188 g of CuCl prepared above, grind them at a grinding speed of 300 r / min, and grinding time of 15 min, heat-treat for 2 h at 380 °C in a nitrogen atmosphere, and immediately after cooling Obtain an adsorbent sample. The adsorption performance of the adsorbent was measured by gravimetric method (this method was used in the following examples), and the loading capacity of copper element in the adsorbent was 12 mmol / g carrier.
[0018] Adsorption experiment: Take 30mg of the above-mentioned adso...
Embodiment 2
[0020] Preparation of porous carbon: Dissolve 1.0g sucrose in 20mL isopropanol, take 2g triblock copolymer F108 (EO 132 PO 50 EO 132 ) and 1 g of triblock copolymer F127 (EO 106 PO 70 EO 106 ) was dissolved in 20mL of isopropanol, benzene was removed in one step in an oven at 130°C and thermal polymerization was carried out, and finally under the protection of inert gas, the temperature was raised to 1000°C for carbonization to obtain porous carbon (with a specific surface area of 3000m 2 / g).
[0021] Preparation of adsorbent: Weigh 1g of porous carbon and 0.792g of CuCl prepared, grind them at a grinding speed of 350r / min, and grinding time of 10min, heat-treat in a nitrogen atmosphere at 350°C for 2h, and obtain Sorbent samples. The loading amount of copper element in the adsorbent is 6mmol / g carrier.
[0022] Adsorption experiment: Take 30 mg of the above-mentioned adsorbent and place it in a high-precision gravimetric adsorption instrument Hiden IGA-100, fill it ...
Embodiment 3
[0024] Preparation of porous carbon: Dissolve 1.0g furfuryl alcohol in 20mL isopropanol, take 1g triblock copolymer F108 (EO 132 PO 50 EO 132 ) was dissolved in 20mL of isopropanol, and the isopropanol was removed in one step in an oven at 150°C and thermally polymerized. Finally, under the protection of inert gas, the temperature was raised to 900°C for carbonization to obtain porous carbon (with a specific surface area of 1000m 2 / g).
[0025] Preparation of adsorbent: Weigh 1g of porous carbon and 0.792g of CuCl, grind them, the grinding speed is 350r / min, the grinding time is 20min, heat treatment in nitrogen atmosphere, 350°C for 4h, and get the adsorbent sample after cooling . The loading amount of copper element in the adsorbent is 8mmol / g carrier.
[0026] Adsorption experiment: Take 30 mg of the above-mentioned adsorbent and place it in a high-precision gravimetric adsorption instrument Hiden IGA-100, fill it with propylene and propane at a rate of 10 mbar / min, ...
PUM
Property | Measurement | Unit |
---|---|---|
adsorption capacity | aaaaa | aaaaa |
adsorption capacity | aaaaa | aaaaa |
adsorption capacity | 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