Method for detecting components of mixed gas in wastewater pool
A mixed gas and component detection technology, applied in chemical instruments and methods, analytical materials, measuring devices, etc., can solve the problem of inability to accurately measure the content of harmful gases in wastewater, achieve good water solubility, wide detection range, and promote penetration.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0021] Step 1. Mix 0.123 g 6-methoxy-2-methylquinoline and 0.543 g iodomethane in anhydrous toluene, heat the mixture at 90°C for 8 h, then cool to room temperature, filter, wash, vacuum Dry to obtain light yellow solid powder.
[0022] Step 2. Dissolve 0.13 g (7)-diethylamino-2-oxo-2H-benzopyran-3-carbaldehyde and 0.1 g of the product obtained in step 1 in absolute ethanol, and stir the mixture at 85°C to reflux After 12 hours, it was cooled to room temperature, and the filtrate was collected by filtration and spin-dried under reduced pressure. Using dichloromethane and methanol with a volume ratio of 20:1 as the eluent, it was separated by silica gel column chromatography and purified to obtain an orange solid powder SO 2 probe.
[0023] Step 3. Add 0.1 g of 3,7-bis(dimethylamine)-5,5-dimethyldibenzo and 8 mL of dry tetrahydrofuran into a dry flask. The solution was cooled to -78°C, 3 mL of tert-butyllithium was added dropwise, stirred for 30 min, heated to room temperatur...
Embodiment 2
[0027] Step 1. Mix 0.2 g 6-methoxy-2-methylquinoline and 0.1 g iodomethane in anhydrous toluene, heat the mixture at 90°C for 6 h, then cool to room temperature, filter, wash, vacuum Dry to obtain light yellow solid powder.
[0028] Step 2, 0.4 g (7)-diethylamino-2-oxo-2H-benzopyran-3-carbaldehyde and 0.5 g of the product obtained in step 1 were dissolved in absolute ethanol, and the mixture was stirred and refluxed at 85 °C After 12 hours, it was cooled to room temperature, and the filtrate was collected by filtration and spin-dried under reduced pressure. Using dichloromethane and methanol with a volume ratio of 20:1 as the eluent, it was separated by silica gel column chromatography and purified to obtain an orange solid powder SO 2 probe.
[0029] Step 3. Add 0.5 g of 3,7-bis(dimethylamine)-5,5-dimethyldibenzo and 10 mL of dry tetrahydrofuran into a dry flask. The solution was cooled to -78°C, 5 mL of tert-butyllithium was added dropwise, stirred for 30 min, heated to ro...
Embodiment 3
[0033] Step 1. Mix 0.6 g 6-methoxy-2-methylquinoline and 0.2 g iodomethane in anhydrous toluene, heat the mixture at 90°C for 10 h, then cool to room temperature, filter, wash, vacuum Dry to obtain light yellow solid powder.
[0034] Step 2, 0.34 g (7)-diethylamino-2-oxo-2H-benzopyran-3-carbaldehyde and 0.3 g of the product obtained in step 1 were dissolved in absolute ethanol, and the mixture was stirred and refluxed at 85 °C After 12 hours, it was cooled to room temperature, and the filtrate was collected by filtration and spin-dried under reduced pressure. Using dichloromethane and methanol with a volume ratio of 20:1 as the eluent, it was separated by silica gel column chromatography and purified to obtain an orange solid powder SO 2 probe.
[0035] Step 3. Add 0.8 g of 3,7-bis(dimethylamine)-5,5-dimethyldibenzo and 10 mL of dry tetrahydrofuran into a dry flask. The solution was cooled to -78°C, 4 mL of tert-butyllithium was added dropwise, stirred for 30 min, heated to ...
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