Treatment with chlorates produced by electrolyzing saltwater
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As the title suggests, after the chlorate is produced at 310, is it possible for colleagues to add formaldehyde to it (before adding HCl), and then not release the gas into the main exhaust duct before it enters the decomposition tank? In this way, could sodium carbonate be formed instead of the decomposed CO2 being released? in order to reduce the consumption of the auxiliary material soda ash
Your idea is quite unusual. So, how will the chlorates in that brackish water be decomposed in the end, and where does the chlorine gas produced go?
Well, those working in the chlor-alkali industry should know, right?
I don’t use formaldehyde here; as soon as it comes out of the anode solution pump, it is heated and acid is added. There’s a chlorate decomposition tank, and chlorine is connected to the main pipeline. If the chlorate content is low, no additives are used; if it’s high, the LSZ agent is added.
Install a chlorate decomposition tank unit
Our factory uses the purchased LSZ reagent to treat and decompose chlorates
Recently, the method of using the new LSZ reagent to decompose chlorates has become very popular. What exactly is LSZ? Does anyone know?
Could any enthusiastic friends of Lsz introduce me?
Friend, could you give a brief introduction?