A heavy metal ion remover with self-flocculation function and its synthesis method
A technology of heavy metal ions and self-flocculation, which is applied in chemical instruments and methods, flocculation/sedimentation water/sewage treatment, water/sludge/sewage treatment, etc., can solve the problem of increased treatment cost and difficulty of treatment process, high heavy metal content, inability to Achieve the effect of good self-flocculation function, large molecular weight and good applicability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0027] Step (1): Add 180g of sodium hydroxide aqueous solution (mass concentration: 3wt.%) to a three-necked flask with magnetic stirring, heat up to 45°C, then add 3g of soluble starch, after stirring evenly, slowly add 25g of epoxy Chloropropane, the system was slowly raised to 55°C and stirred for 8 hours. After the reaction was completed, it was cooled to room temperature, filtered, washed with distilled water, ethanol, and acetone in sequence, and vacuum-dried to obtain the target product AP1.
[0028] Step (2): Add 90g of sodium hydroxide aqueous solution (mass concentration is 0.5wt.%) to the three-necked flask with magnetic stirring, heat up to 60°C, then add 3g of the product AP1 synthesized in step (1), and stir evenly , slowly drop 9g of diethylenetriamine, and the system was stirred and reacted at 60-70°C for 4 hours. After the reaction was completed, it was cooled to room temperature, filtered, washed with distilled water, ethanol, and acetone in sequence, and va...
Embodiment 2
[0033] Step (1): Add 200g of sodium hydroxide aqueous solution (mass concentration: 2wt.%) to a three-necked flask with magnetic stirring, heat up to 55°C, then add 3g of soluble starch, after stirring evenly, slowly add 30g of epoxy Chloropropane, the system was slowly raised to 60°C and stirred for 6 hours. After the reaction was completed, it was cooled to room temperature, filtered, washed with distilled water, ethanol, and acetone in turn, and vacuum-dried to obtain the stage target product BP1.
[0034] Step (2): Add 120g of sodium hydroxide aqueous solution (mass concentration is 1.5wt.%) to the there-necked flask with magnetic stirring, heat up to 65°C, then add 3g of the product BP1 synthesized in step (1), and stir evenly 12 g of triethylenetetramine was slowly added dropwise, and the system was stirred and reacted at 70° C. for 6 hours. After the reaction was completed, it was cooled to room temperature, filtered, washed with distilled water, ethanol, and acetone i...
Embodiment 3
[0039] Step (1): Add 240g of sodium hydroxide aqueous solution (mass concentration is 4wt.%) to the three-necked flask with magnetic stirring, heat up to 55°C, then add 3g of soluble starch, after stirring evenly, slowly add 40g of epoxy Chloropropane, the system was slowly raised to 70°C and stirred for 12 hours. After the reaction was completed, it was cooled to room temperature, filtered, washed with distilled water, ethanol, and acetone in sequence, and vacuum-dried to obtain the stage target product CP1.
[0040] Step (2): Add 150g potassium hydroxide aqueous solution (mass concentration is 2wt.%) to the there-necked flask with magnetic stirring, heat up to 65°C, then add 3g of the product CP1 synthesized in step (1), after stirring evenly, 15 g of tetraethylenepentamine was slowly added dropwise, and the system was stirred and reacted at 75-80° C. for 8 hours. After the reaction was completed, it was cooled to room temperature, filtered, washed with distilled water, eth...
PUM
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