1,4-Trihydroxyethylbenzyldiammonium Sulfate, 1,3,5-Trihydroxyethylbenzyltriammonium Sulfate and Synthesis and Application
A technology of trihydroxyethyl diammonium and trihydroxyethyl diammonium, applied in 1,4-trihydroxyethyl diammonium sulfate, 1,3,5-trihydroxyethyl diammonium sulfate In the field of salt and synthesis and application, it can solve the problems of low resistance to environmental influence, difficult to digest gypsum saturation, and the decline in the quality of desulfurized gypsum, and achieve the effects of strong environmental adaptability, high adsorption saturation, and large-scale production
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Embodiment 1
[0054] In this example, 1,4-p-dichlorobenzyl, acetonitrile, triethanolamine, sulfuric acid, etc. are used as main raw materials, and are prepared by chemical synthesis method under certain conditions. Specifically, it includes the following main steps:
[0055] (1) 1 part of 1,4-p-dichlorobenzyl was added to 2.5 parts of acetonitrile solution, fully stirred, and dispersed uniformly;
[0056] (2) add 2.2 parts of triethanolamine again, stir simultaneously and heat the temperature to 80 DEG C and reflux for 8h, the reaction equation is:
[0057]
[0058] (3) be cooled to room temperature naturally, and generate a large amount of 1,4-trihydroxyethylbenzyldiammonium chloride white precipitate, obtain filter cake after filtration, and filter cake is washed 3 times with acetonitrile solution;
[0059] (4) under 50 ℃ of vacuum conditions, the filter cake was dried for 8 hours to obtain 1,4-trihydroxyethylbenzyldiammonium chloride;
[0060] (5) under stirring condition, the vitri...
Embodiment 2
[0068] In this example, 1,3,5-tris(bromomethyl)benzene, acetonitrile, triethanolamine, sulfuric acid, etc. are used as main raw materials, and are prepared by chemical synthesis method under certain conditions. Specifically, it includes the following main steps:
[0069] (1) 1 part of 1,3,5-tris(bromomethyl)benzene was added to 2.6 parts of acetonitrile solution, fully stirred, and dispersed uniformly;
[0070] (2) add 3.3 parts of triethanolamine again, stir simultaneously and the temperature is heated to 80 DEG C and refluxed for 8h, the reaction equation is:
[0071]
[0072] (3) be cooled to room temperature naturally, and generate a large amount of 1,3,5-trihydroxyethylbenzyltriammonium bromide white precipitate, obtain filter cake after filtration, and filter cake is washed 3 times with acetonitrile solution;
[0073] (4) under 50 ℃ of vacuum conditions, the filter cake was dried for 8 hours to obtain 1,3,5-trihydroxyethylbenzyltriammonium bromide;
[0074] (5) unde...
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