Organic silicate comprising ether, preparing process and application thereof
A technology of organosilicate and acrylic acid, applied in the fields of organic chemistry, organic silicon compounds, chemical instruments and methods, etc., can solve the problems of poor corrosion inhibition effect of organosilicate and can not meet industrial production, and avoid eutrophication. Pollution, good corrosion inhibition effect, not easy to silicate scale effect
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2006-02-01
- Estimated Expiration
- Not applicable · inactive patent
Smart Images
Figure 1 Figure 2
Abstract
Description
technical field
[0001] The invention relates to an ether-containing organic silicate and its preparation and application method. technical background
[0002] With the rapid development of industry and economy, the eutrophication of the water environment is becoming more and more serious, causing frequent occurrence of red tides in coastal waters, rivers and lakes, causing serious deterioration of water quality, mass death of fish and shrimp, and heavy economic losses. The main reason for the frequent occurrence of red tides is the high concentration of phosphate in the water. Therefore, reducing the use and discharge of phosphate is of great significance for alleviating and ultimately avoiding the occurrence of red tides in water bodies. Phosphorus-containing water treatment agents are widely used because of their excellent corrosion and scale inhibition properties. How to reduce and avoid the use of phosphorus-containing water treatment agents has become an urgent problem...
Examples
Embodiment 1
[0026] This embodiment is the preparation of N, N'-two (γ-propyl sodium silicate)-dipolyoxyethylene ether {[(NaO) 3 SiCH 2 CH 2 CH 2 NH] 2 (CH 2 CH 2 OCH 2 CH 2 )}.
[0027] Add 95.7 g (0.42 mol) of γ-aminopropyltriethoxysilane with a molecular weight of 221.0 and a purity of 97% into a 250 mL 4-necked round-bottomed flask equipped with mechanical stirring, start stirring, and protect with nitrogen at the same time. Slowly heat the flask for 15 minutes to make the reaction materials warm up to 105°C, and weigh α, ω-dichlorodipolyoxyethylene ether (Cl-CH 2 CH 2 OCH 2 CH 2 -Cl) 29.8g (0.2mol) is placed in the dropping funnel, when the reaction flask material temperature is 105 ℃, begin to slowly use 2 hours to evenly drop in the reaction flask, the reaction temperature of the dropping process is maintained at 105~ At 115°C, α,ω-dichlorotripolyoxyethylene ether was added dropwise, and then reacted at 110-120°C for 2 hours.
[0028] After the reaction is complete, red...
Embodiment 2
[0033] The present embodiment is the preparation of N, N'-two (gamma-propyl sodium silicate)-pentapolyoxyethylene ether {[(NaO) 3 SiCH 2 CH 2 CH 2 NH] 2 CH 2 CH 2 (OCH 2 CH 2 ) 4}.
[0034]Weigh respectively 95.7g (0.42mol) of γ-aminopropyltriethoxysilane with a purity of 97%, and 57.3g of α, ω-dichloropentapolyoxyethylene ether with a purity of 275.0% according to the examples 1, to obtain 100.7g product (yield 82%).
Embodiment 3
[0036] The present embodiment is the preparation of N, N'-bis(γ-propyl sodium silicate)-octoxyethylene ether {[(NaO) 3 SiCH 2 CH 2 CH 2 NH] 2 CH 2 CH 2 (OCH 2 CH 2 ) 7}.
[0037] Take by weighing 95.7g (0.42mol) of γ-aminopropyltriethoxysilane with a purity of 97% and 95% α, ω-dichlorooctoxyethylene ether 85.7g with a purity of 97%, and the operation steps are according to Example 1 , to obtain 111.9 g of product (yield 75%).