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Imidazoline Quaternary Ammonium Salt Corrosion Inhibitor
[Physical and chemical properties] This type of corrosion inhibitor has no special pungent odor, good thermal stability, and low toxicity
[Preparation method] (1) Synthesis of imidazoline quaternary ammonium salt corrosion inhibitor
① imidazoline Synthesis of imidazoline amide is dehydrated by dehydration and cyclization further formed
②Synthesis of imidazoline quaternary ammonium salt.
The quaternization reaction of imidazoline is further carried out: when the temperature is 100-120° C.
(2) Preparation example
①Add 0.
②Li Bang used naphthenic acid with an acid value (KOH) of 190mg/g as a raw material to react with polyethylene polyamine to synthesize a cycloalkylimidazoline intermediate, and then use diethyl sulfate to quaternize the intermediate.
The best synthesis conditions are: the first step, naphthenic acid: diethylene triamine (molar ratio) = 1: (1.
③Song Sasha uses benzoic acid and triethylenetetramine as raw materials to synthesize imidazoline precursors, and modifies them with 1-chloro3-phenylpropane to prepare imidazoline quaternary ammonium salt corrosion inhibitors: combine benzoic acid and triethylenetetramine The amine was added to a 250 mL three-necked flask at a molar ratio of 1:1.
④ Zhang Guanghua prepared 2-aminoethyl heptadecenyl by reacting oleic acid (industrial product, the fraction obtained under reduced pressure 180~230℃/mmHg), diethylenetriamine and benzyl chloride in xylene solution Imidazoline quaternary ammonium salt
Put oleic acid, diethylenetriamine, xylene, and catalyst into the reaction kettle, and install a water separator to return the reactants to separate water