Method for using pennisetum hydridum lignin for preparation of active carbon and application of active carbon
A technology for preparing activated carbon and giant juncao, which is applied in the fields of lignin derivatives, chemical instruments and methods, organic chemistry, etc., can solve the problems of high-value utilization of wood fiber, achieve enhanced impregnation effect, shorten reaction time, The effect of increasing the number
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0036] Extraction and pretreatment with benzene-alcohol and hot water, and sieve through a sample sieve to obtain 40-60 mesh giant Juncao grass powder. Cellulose, hemicellulose and lignin were extracted by microwave-alkali-alcohol method.
[0037] The specific extraction steps are as follows: (1) Raw material pretreatment: pulverize the air-dried giant fungus grass, and obtain 40-60 mesh grass powder through a sample sieve, add 150mL benzene-alcohol mixture to the Soxhlet extractor, and the Extract from grass powder for 5-7h for dewaxing, add water to the dewaxed Jujuncao at a mass ratio of 1: (20-30), wherein the mass of Jujuncao is 10g, extract at 80-90°C After 2-4 hours, the protein and pectin in the giant juncao are further removed, filtered, and dried to obtain the pretreated giant juncao, and then passed through a 40-60 mesh sieve to obtain a giant juncao powder.
[0038] Wherein, the benzene-alcohol mixed solution is a mixed solution of toluene and ethanol at a volume ...
Embodiment 2
[0046] According to the impregnation ratio of 3:1, impregnate the hydrothermal coke with 85% phosphoric acid (the preparation method of the hydrothermal coke is the same as that in Example 1). After fully stirring and impregnating for 2 hours, the impregnated hydrothermal coke was dried at 90°C. The dried product was transferred to a tube-type resistance furnace, and the temperature was raised to 450°C at a heating rate of 10°C / min, and the activation reaction was maintained for 1.5 hours. After reaching the reaction time, it was naturally cooled to room temperature. The entire activation and cooling process was carried out in a nitrogen atmosphere. The obtained solid was ground in a mortar, activated with 1 mol / L HCl solution for 1 h while boiling, filtered, the filtrate was washed with deionized water until neutral, and dried at 105°C to obtain activated carbon. Its specific surface area and total pore volume reached the largest, respectively 1806m 2 / g and 1.12cm 3 / g, ...
Embodiment 3
[0049] According to the impregnation ratio of 2:1, impregnate the hydrothermal coke with 75% phosphoric acid (the preparation method of the hydrothermal coke is the same as that in Example 1). After fully stirring and impregnating for 1.5 hours, the impregnated hydrothermal coke was dried at 90°C. The dried product was transferred to a tube-type resistance furnace, and the temperature was raised to 350°C at a heating rate of 10°C / min, and the activation reaction was maintained for 1.5 hours. After reaching the reaction time, it was naturally cooled to room temperature. The entire activation and cooling process was carried out in a nitrogen atmosphere. The obtained solid was ground in a mortar, activated with 1 mol / L HCl solution for 1 h while boiling, filtered, the filtrate was washed with deionized water until neutral, and dried at 105°C to obtain activated carbon. Its specific surface area and total pore volume reached the largest, respectively 1756m 2 / g and 1.05cm 3 / g...
PUM
Property | Measurement | Unit |
---|---|---|
pore size | aaaaa | aaaaa |
specific surface area | aaaaa | aaaaa |
pore size | 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