Barium Carbonate --> Barium Nitrate
#61
Posted 11 October 2007 - 07:11 PM
Assuming I am trying to make 1l of 25% concentration:
(.70)V1=(.25)1000ml---->V1=357ml
Vs=1000-357---->643ml
Therefore I add 643ml water to 357ml of HNO3?
#62
Posted 12 October 2007 - 07:56 AM
#63
Posted 12 October 2007 - 01:02 PM
I`ll leave the maths to you, but always add the acid to the water, NEVER add water to the acid!
Ooops, typed it wrong. Was just trying to get ratios. I knew to always add acid to water, but should have double checked what I wrote before posting.
#64
Posted 12 October 2007 - 02:24 PM
I just don`t wanna see ya get hurt that`s all, so it seemed worth a mention
#65
Posted 12 October 2007 - 07:01 PM
#66
Posted 12 October 2007 - 07:19 PM
Just another safety note: when you add the solid barium carbonate to the dilute nitric acid, you will see vigorous effervescence (fizzing) caused by the rapid evolution of carbon dioxide gas. The airborne aerosol produced by this will be likely to contain toxic barium nitrate, aswell as nitric acid. So, it would be advisable to carry-out the reaction outside, or cover the reaction vessel with a clear plastic bag in order to contain the mist. Only add the barium carbonate in small quantities at a time. I assume you have the appropriate safety gear- safety specs and a respirator?
I'm all set for safety equipment. I did this reaction before, only I used the 70%HNO3 as is, no diluting. I did end up adding a considerable amount of water to dissolve all the nitrate though. This time I would like to start with a dilted solution and I will be doing smaller batches.
#67
Posted 12 November 2007 - 07:31 PM
#68
Posted 13 November 2007 - 07:26 PM
#69
Posted 14 November 2007 - 10:45 AM
if you add Campden tablets that also works by the RXN: SO2 + 2H2S = 2H2O + 3S.
after Either of these methods you Will need to filter the liquid away from the PPT.
#70
Posted 14 November 2007 - 04:29 PM
#71
Posted 14 November 2007 - 04:56 PM
and don`t worry that the H2O2 is more than likely stabilised with Phosphoric acid, yes it`s a nasty tribasic acid and as good as Sulphuric for most things anyday of the week!
it also will react with the barium to make an insoluble PPT, it`s only a trace amount they put in anyway to keep its shelf life, but against Barium... it`s got No chance
(3Ba 2+) + (2PO4 3-) = Ba3(PO4)2
Edited by YT2095, 14 November 2007 - 05:00 PM.
#72
Posted 15 November 2007 - 07:57 PM
#73
Posted 19 November 2007 - 10:58 PM
I've done the exact same many times and never had problems with odour with the final product. If you heat it properly after the reaction has taken place, both the acid and any sulfur traces should disappear.
I'm not sure what exactly you mean by heating properly. I boiled off all the water after dissolving the barium nitrate and filtering... I have the crystals in a tray and it still stinks I cranked up the heat in my drying box today (vented outside) and am hoping to drive off the smell. Is it possible that the H2S is caught in between the crystals? I was thinking of milling the crystals and then continuing to air them out as a possible solution.
#74
Posted 20 November 2007 - 07:57 AM
cracking the crystals in a mill and drying again will remove it and have the added effect of releasing trapped liquid in them also leaving a drier product.
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