From: NEAL LANGERMAN <neal**At_Symbol_Here**CHEMICAL-SAFETY.COM>
Subject: Re: [DCHAS-L] Nitrogen tri-Iodide
Date: Fri, 22 Dec 2017 17:27:16 +0000
Reply-To: ACS Division of Chemical Health and Safety <DCHAS-L**At_Symbol_Here**PRINCETON.EDU>
Message-ID: CAOo07Zrn8NmM8TPT2i0sMVYW_RfDsyiNq==+SznK3Sk+M=A2HA**At_Symbol_Here**mail.gmail.com
In-Reply-To
Triiodoammonium bicarbonate?
Ernest et al,Sodium Bicarbonate,,of course in the right 1:1 or more concentrations,might chnge the pH enough to make a difference.How do you get A Nitrogen atom or radical to react as a covalent bond to three Iodide radicals? This one I'm not of a chemist to understand. .If anyone was hurt or injured, I might be able to suggest ways to help.AlanAlan H.Hall,M.D.MedicalToxicologist--- For more information about the DCHAS-L e-mail list, contact the Divisional secretary at secretary**At_Symbol_Here**dchas.org Follow us on Twitter **At_Symbol_Here**acsdchasOn Fri, Dec 22, 2017 at 10:32 AM, Ernest Lippert <ernielippert**At_Symbol_Here**toast.net> wrote:Chemical Safety headline:'THE SUBSTANCE EMITTED A PURPLE HAZE EACH TIME IT ACTIVATED AND IT SOUNDED LIKE A .22' Tags: us_OR, public, release, response, bomb, sodium_bicarbonateMost probably Nitrogen tri-Iodide. Why would sodium bicarbonate neutralize it? I don't see the chemistry behind it.Ernie Lippert--- For more information about the DCHAS-L e-mail list, contact the Divisional secretary at secretary**At_Symbol_Here**dchas.org Follow us on Twitter **At_Symbol_Here**acsdchas
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