Non-phosphate corrode-releasing antisludging agent and method for synthesizing same
A phosphorus-free corrosion and scale inhibitor technology, applied in chemical instruments and methods, descaling and water softening, water/sludge/sewage treatment, etc., can solve problems that have not been reported in the literature, and achieve increased activation energy, Raw materials are readily available and the effect of slowing down the corrosion rate
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Embodiment 1
[0023] Example 1: Preparation of N-(1-carboxy-3-methoxy-3-carbonylpropyl)-N'-(2-thioformyl) ethylenediamine sodium dimethyl sulfonate (CsEM2S)
[0024]
[0025] Dissolve 13g (0.1mol) of monomethyl maleate in solvent (water and ethanol) and add dropwise to 6g (0.1mol) of ethylenediamine, heat and reflux for 2-3 hours, cool to 40-60°C, drop into An aqueous solution containing 26.8g (0.2mol) of sodium hydroxymethanesulfonate was stirred and reacted for 6 to 12 hours. After the reaction was completed, the pH was adjusted to about 10 with 1mol / L NaOH, the temperature was lowered to below 10°C, and an ethanol solution of carbon disulfide (6mL +15mL). Control the temperature not to be higher than 10° C., react for 2 to 4 hours, and obtain the product CsEM2S as an orange-yellow liquid with a solid content of ≥ 30%. The infrared spectrum data of the solid substance are shown in Table 1.
Embodiment 2
[0026] Embodiment 2: the preparation of N-carboxymethyl-N'-(2-thioformyl) ethylenediamine sodium dimethyl sulfonate (CsEC2S)
[0027]
[0028] Add 9.5g (0.1mol) of chloroacetic acid aqueous solution dropwise to 6g (0.1mol) of ethylenediamine, heat to reflux for 1-2 hours, cool to 40-60°C, dropwise add 26.8g (0.2mol) of hydroxymethyl The aqueous solution of sodium sulfonate was stirred and reacted for 6-12 hours. After the reaction was completed, the pH was adjusted to about 10 with 1mol / L NaOH, the temperature was lowered to below 10°C, and an ethanol solution of carbon disulfide (6mL+15mL) was added dropwise. Control the temperature not higher than 10°C, react for 2-4 hours, and obtain the orange liquid of the product CsEC2S, which is diluted with water to a solid content ≥ 30%. The infrared spectrum data of the solid substance are shown in Table 1.
Embodiment 3
[0029] Example 3: N 1 -(1-carboxy-3-methoxy-3-carbonylpropyl)-N 3 Preparation of -(2-thioformyl) diethylene triamine sodium dimethyl sulfonate (Cs2EM2S)
[0030]
[0031] Dissolve 13g (0.1mol) of monomethyl maleate in a solvent (water and ethanol) and add dropwise to 10.3g (0.1mol) of diethylenetriamine, heat to reflux for 2 to 3 hours, and cool to 40 to 60°C. Add dropwise an aqueous solution containing 26.8g (0.2mol) sodium hydroxymethanesulfonate, stir and react for 6 to 12 hours, after the reaction is completed, adjust the pH to about 10 with 1mol / L NaOH, lower the temperature to below 10°C, and add dropwise an ethanol solution of carbon disulfide (6mL+15mL). Control the temperature not higher than 10°C, react for 2-4 hours, and obtain the product Cs2EM2S as an orange-yellow viscous liquid with a solid content of ≥30%. The infrared spectrum data of the solid substance are shown in Table 1.
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