Preparation of 2-Mercaptopyrimidine modified magnetic cotton-straw bast adsorbent
A technology of mercaptopyrimidine and cotton stalk bark, which is applied in the field of environment and chemistry, can solve the problems of difficult solid-liquid separation of adsorbents and hinder the progress of adsorption technology, and achieve good physical and chemical stability, excellent mechanical strength, and good desorption performance.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0024] (1) Preparation of oxidized cotton stalk husk: In the reactor, add potassium permanganate: 7g, deionized water: 76 mL, stir to dissolve, add sulfuric acid: 4 mL, mix well, then add pretreated cotton stalk husk: 10g , soaked at room temperature for 6 h, boiled for 10 min, washed with deionized water until neutral after cooling, separated from solid and liquid, and dried to obtain oxidized cotton stalk bark;
[0025] (2) Preparation of magnetic cotton stalk skin: In the reactor, add deionized water: 63 mL, ferric ion: 5g, ferrous ion: 2g, neodymium ion: 12g, sodium tetraborate: 5g, after ultrasonic dissolution , add oxidized cotton stalk skin: 13g, adjust the pH between 10 and 12 with NaOH under stirring, raise the temperature to 90±2°C, keep stirring, and reflux for 6.5 hours. The whole reaction process is carried out under argon atmosphere, and the reaction is over After cooling to room temperature, solid-liquid separation, washing, drying, to obtain magnetic cotton sta...
Embodiment 2
[0029] (1) Preparation of oxidized cotton stalk husk: In the reactor, add potassium permanganate: 10g, deionized water: 74 mL, stir to dissolve, add sulfuric acid: 5.5 mL, mix well, then add pretreated cotton stalk husk: 6g , soaked at room temperature for 6 h, boiled for 10 min, washed with deionized water until neutral after cooling, separated from solid and liquid, and dried to obtain oxidized cotton stalk bark;
[0030] (2) Preparation of magnetic cotton stalk skin: In the reactor, add deionized water: 66 mL, ferric ion: 4g, ferrous ion: 3g, neodymium ion: 8g, sodium tetraborate: 4g, after ultrasonic dissolution , add oxidized cotton stalk skin: 15g, adjust the pH between 10 and 12 with NaOH under stirring, raise the temperature to 90±2°C, keep stirring, and reflux for 6 hours. The whole reaction process is carried out in an argon atmosphere. After the reaction , cooled to room temperature, solid-liquid separation, washing, drying, to obtain magnetic cotton stalk skin;
...
Embodiment 3
[0034] (1) Preparation of oxidized cotton stalk husk: In the reactor, add potassium permanganate: 5g, deionized water: 80 mL, stir to dissolve, add sulfuric acid: 5mL, mix well, then add pretreated cotton stalk husk: 9g, Soak at room temperature for 6 hours, boil for 10 minutes, wash with deionized water until neutral, separate solid and liquid, and dry to obtain oxidized cotton stalk bark;
[0035] (2) Preparation of magnetic cotton stalk skin: In the reactor, add deionized water: 60mL, ferric ion: 6g, ferrous ion: 2g, trivalent neodymium ion: 13g, sodium tetraborate: 6g, after ultrasonic dissolution, Add oxidized cotton stalk skin: 10g, adjust the pH between 10 and 12 with NaOH under stirring, raise the temperature to 90±2°C, keep stirring, and reflux for 7 hours. The whole reaction process is carried out in an argon environment. After the reaction, cooling to room temperature, solid-liquid separation, washing, and drying to obtain magnetic cotton stalk skins;
[0036] (3) ...
PUM
Property | Measurement | Unit |
---|---|---|
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