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Laboratory Tips Safety proceedures, test reagents, drilling rubber stoppers, bending glass tubes, etc. Contributed to by chemists.

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Old 2003-11-28, 19:12
IncognitoSTchick IncognitoSTchick is offline
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Default THANK YOU ALL~!

a HUGE thanks to those that helped out with question(s) i asked in the thread 'awesome iodine extraction' (oct 03)

A few thought the problem was in the rxn, not the crystal extraction....well ST KNEW it couldnt be in the rxn, considering all worked well (for a few years)until one day couldnt get anymore IO. Searching away, ST mentioned finding this site, (been addicted ever since to many areas of the community).

Anyways, problem was a couple of things in STs method of IO extraction process(practice DOES make near perfect, heh)

first, ST was told to put 2x amt of peroxide to the IO. THEN ST used a metal strainer..haha...:shrugs:

then, used pantyhose (not bad!)

also, ST only let sit for about an hour. letting it sit for a lot longer (ST now just lets it sit for a full day)was one key thing, so far, besides another piece of awesome advice givin by gottagogo (acidify first..thank you man!) AND last but definitely not LEAST of problems (probably worst) it was always wet when used. ST thought it was dry...but after continuing research ST found out that drying took awhile.

anyway...thanks guys...\m/

****and gottagogo, if i would have explained exactly what i meant about the 'push/pull' and so on...woulda took a LOT of space...get a hold of me,via email..(link is in profile? i believe?) ive seen this method on a site i believe was mentioned in this forum, which i thought was wild, hah..but awesome.
 
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