CHRIS25
National Hazard
Posts: 951
Registered: 6-4-2012
Location: Ireland
Member Is Offline
Mood: No Mood
|
|
Myth busted - Epsom not good source of Mg Sulphate
MgSO4 - a very much needed dssicant and I have tried to use it a number of times, became suspicious when absolutely zero moisture found in
my "magnesium sulphate" (which I dehydrated many weeks ago), after a week in a place where it should have by now been soaked.
Magnesium sulphate is soluble in water 30g/100mLs at 20c approx and it did dissolve in water; and magnesium oxide is not soluble in alcohol. Because
the box says "Epsom Salts magnesium Sulphate" and then in Contents says Magnesium Oxide (no percentage or w/w given at all), I was surprised since the
oxide is not a cheap chemical. Here is an image of the white offender in 38% alchohol (no I don't drink the stuff it was a gift years ago and I have
used it only for chemistry and nasty cuts). Anyway It refuses to dissolve. It dissolved with vigorous stirring in a 1.8M sulphuric acid concentration
giving more credence to a large source of Oxide, so it does appear that this foilage growth Epsom salt is not a good source of Magnesium sulphate for
the chemist as is popularly suggested, maybe for the plants yes. The end result is that it simply does not absorb moisture at all - so how much of
this stuff is actually sulphate is questionable.
Anybody have any comments? and don't mourn the waste of dry gin it's not good for you anyway.
‘Calcination… is such a Separation of Bodies by Fire, as makes ‘em easily reducible into Powder; and for that reason ‘tis call’d by some
Chymical Pulverization.’ (John Friend, Chymical Lectures London, 1712)
Right is right, even if everyone is against it, and wrong is wrong, even if everyone is for it. (William Penn 1644-1718)
The very nature of Random, Chance development precludes the existence of Order - strange that our organic and inorganic world is so well defined by
precision and law. (me)
|
|
|
blogfast25
International Hazard
Posts: 10562
Registered: 3-2-2008
Location: Neverland
Member Is Offline
Mood: No Mood
|
|
Hmmm... Epsom salt is a hydrate of magnesium sulphate. As such it's not a desiccant. To make it one, strong heating is needed to obtain the anhydrous
form, which is strongly hygroscopic and used as a desiccant.
MgO is probably present in very small amounts, as an anti-caking agent. 0.5 % or so. It's used also in washing soda, to prevent lumping (caking).
Gin is only about 40 % ethanol so shouldn't be described as 'alcohol' (drinking alcohol yes, 'pure ethanol' not)
To obtain purer MgSO4 hydrate from garden grade Epsom salts, dissolve in hot water and filter off the MgO. Then crystallise. Acc. wiki MgSO4 has a
decent dependence of solubility on temperature, so thermal recrystallizing is possible.
Also, next time you desiccate it: weigh before and after. The calculate if weight loss more or less corresponds to MgSO4.7H2O === > MgSO4 + 7 H2O
[Edited on 8-5-2014 by blogfast25]
|
|
|
Magpie
lab constructor
Posts: 5939
Registered: 1-11-2003
Location: USA
Member Is Offline
Mood: Chemistry: the subtle science.
|
|
Quote: Originally posted by CHRIS25  | ... (which I dehydrated many weeks ago), after a week in a place where it should have by now been soaked.
|
If you did indeed dehydrate it then it would be a white powder. When it absorbs water to the heptahydrate then it is still a white powder. How do
you know that it is not absorbing water?
see http://en.wikipedia.org/wiki/Magnesium_sulfate
The single most important condition for a successful synthesis is good mixing - Nicodem
|
|
|
CHRIS25
National Hazard
Posts: 951
Registered: 6-4-2012
Location: Ireland
Member Is Offline
Mood: No Mood
|
|
Yes I know, but I did think that I had dehydrated it because it was in an oven at 110c for about 1 hour and it certainly changed appearance from
crystals to a fine powder after a little crushing. Anyway I will try what you suggested.
‘Calcination… is such a Separation of Bodies by Fire, as makes ‘em easily reducible into Powder; and for that reason ‘tis call’d by some
Chymical Pulverization.’ (John Friend, Chymical Lectures London, 1712)
Right is right, even if everyone is against it, and wrong is wrong, even if everyone is for it. (William Penn 1644-1718)
The very nature of Random, Chance development precludes the existence of Order - strange that our organic and inorganic world is so well defined by
precision and law. (me)
|
|
|
Metacelsus
International Hazard
Posts: 2537
Registered: 26-12-2012
Location: Boston, MA
Member Is Offline
Mood: Double, double, toil and trouble
|
|
My epsom salts (a different brand) work just fine for dehydrating and using as a drying agent. They also are reasonably pure (>98%) magnesium
sulfate. I think the remainder is mostly sodium sulfate, based on a flame test.
|
|
|
CHRIS25
National Hazard
Posts: 951
Registered: 6-4-2012
Location: Ireland
Member Is Offline
Mood: No Mood
|
|
Well because after a few weeks I would have expected at the least, not to have been able to shake the 'powder' around so freely on the glass, plus I
used it as a desicant to absorb moisture from precipitated silicon dioxide when I put it into a homemade hot chamber - after one hour I became
suspicious, so I swapped this for sodium sulphate that I had made and within another 30 minutes the sodium sulphate was already half its volume with
moisture.
‘Calcination… is such a Separation of Bodies by Fire, as makes ‘em easily reducible into Powder; and for that reason ‘tis call’d by some
Chymical Pulverization.’ (John Friend, Chymical Lectures London, 1712)
Right is right, even if everyone is against it, and wrong is wrong, even if everyone is for it. (William Penn 1644-1718)
The very nature of Random, Chance development precludes the existence of Order - strange that our organic and inorganic world is so well defined by
precision and law. (me)
|
|
|
Magpie
lab constructor
Posts: 5939
Registered: 1-11-2003
Location: USA
Member Is Offline
Mood: Chemistry: the subtle science.
|
|
My information says that dehydration should be at "200°C and red heat." I would try 200°C overnight.
[Edited on 8-5-2014 by Magpie]
The single most important condition for a successful synthesis is good mixing - Nicodem
|
|
|
S.C. Wack
bibliomaster
Posts: 2419
Registered: 7-5-2004
Location: Cornworld, Central USA
Member Is Offline
Mood: Enhanced
|
|
You have to weigh.
|
|
|
CHRIS25
National Hazard
Posts: 951
Registered: 6-4-2012
Location: Ireland
Member Is Offline
Mood: No Mood
|
|
Ah this is the first time I did not search on this forum: http://www.sciencemadness.org/talk/viewthread.php?tid=9429 and then here: http://www.lycaeum.org/mv/mu/MgSO4.html I simply forgot, actually believing that I knew what I was doing when I 'tried' to dehydrate the
product. I never bothered doing a research on this thinking that it was straightforward - that will teach me, when I think I know it....double check.
[Edited on 8-5-2014 by CHRIS25]
‘Calcination… is such a Separation of Bodies by Fire, as makes ‘em easily reducible into Powder; and for that reason ‘tis call’d by some
Chymical Pulverization.’ (John Friend, Chymical Lectures London, 1712)
Right is right, even if everyone is against it, and wrong is wrong, even if everyone is for it. (William Penn 1644-1718)
The very nature of Random, Chance development precludes the existence of Order - strange that our organic and inorganic world is so well defined by
precision and law. (me)
|
|
|
S.C. Wack
bibliomaster
Posts: 2419
Registered: 7-5-2004
Location: Cornworld, Central USA
Member Is Offline
Mood: Enhanced
|
|
PS: In advance, disappointing results on drying your gin with very dry MgSO4 should not come as a surprise, but good luck anyways.
|
|
|
Magpie
lab constructor
Posts: 5939
Registered: 1-11-2003
Location: USA
Member Is Offline
Mood: Chemistry: the subtle science.
|
|
I have not tried dehydrating spirits with drying agents on the first dehydration. 62% water is a lot of water and it would take a lot of anhydrous
MgSO4 even if it does work. Do the math and you will see (hint: use the molecular wts at the bottom of your tech info link).
When I was making absolute alcohol from vodka I would fractional distill first to obtain the azeotrope which is only 5% water. Then I would dewater
further by distillation over lime (CaO) which would take it to ~1% water. Final polishing is then done with 3A molecular sieves which gives very near
absolute alcohol.
I later shortened the above procedure by starting with Everclear which is a spirit of 5% water. Praise be to those states selling Everclear!
There are other methods involving elemental Na, etc, but I have never tried those.
The single most important condition for a successful synthesis is good mixing - Nicodem
|
|
|
CHRIS25
National Hazard
Posts: 951
Registered: 6-4-2012
Location: Ireland
Member Is Offline
Mood: No Mood
|
|
Hey I was not trying to dry Gin! (it says it's dry on the bottle anyway ); ?
‘Calcination… is such a Separation of Bodies by Fire, as makes ‘em easily reducible into Powder; and for that reason ‘tis call’d by some
Chymical Pulverization.’ (John Friend, Chymical Lectures London, 1712)
Right is right, even if everyone is against it, and wrong is wrong, even if everyone is for it. (William Penn 1644-1718)
The very nature of Random, Chance development precludes the existence of Order - strange that our organic and inorganic world is so well defined by
precision and law. (me)
|
|
|
blogfast25
International Hazard
Posts: 10562
Registered: 3-2-2008
Location: Neverland
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by Cheddite Cheese | | My epsom salts (a different brand) work just fine for dehydrating and using as a drying agent. They also are reasonably pure (>98%) magnesium
sulfate. I think the remainder is mostly sodium sulfate, based on a flame test. |
Same here. It's remarkably clean for a garden grade.
| Quote: Originally posted by Magpie | My information says that dehydration should be at "200°C and red heat." I would try 200°C overnight.
|
Red heat??? I've used an electrical hot plate on max. No problem to full dehydration (weight loss verified).
If you're going to waste perfectly good distilled damnation, please quote me for what you have. 
I'm afraid no myth was busted in the making of this thread!
[Edited on 9-5-2014 by blogfast25]
|
|
|
Tsjerk
International Hazard
Posts: 3026
Registered: 20-4-2005
Location: Netherlands
Member Is Offline
Mood: Mood
|
|
Microwaving is the way to go when drying salts! Works good for Na2SO4 and MgSO4 at least. I always used two glass bowls with the open side against
each other. This prevents the violent splattering to leave the containment but allows the water to leave.
Three minutes maximum power, followed by some cooling and you have a bone dry salt. You do have to scrape it from the bowl, so won't get everything
off, but if you just use the same bowl every time this shouldn't be a problem.
|
|
|
CHRIS25
National Hazard
Posts: 951
Registered: 6-4-2012
Location: Ireland
Member Is Offline
Mood: No Mood
|
|
Well I guess, as always, I presumed too much, have not quite cultivated the discipline of Empiricism. Anyway, I heated for one hour at 240c, crushed,
heated another hour, crushed, then heated another hour - it's anhydrous definitely. It's a fine white powder, disturb it and it really fills the air
so I did a good job. You can feel it soak up the sweat on your hand.
‘Calcination… is such a Separation of Bodies by Fire, as makes ‘em easily reducible into Powder; and for that reason ‘tis call’d by some
Chymical Pulverization.’ (John Friend, Chymical Lectures London, 1712)
Right is right, even if everyone is against it, and wrong is wrong, even if everyone is for it. (William Penn 1644-1718)
The very nature of Random, Chance development precludes the existence of Order - strange that our organic and inorganic world is so well defined by
precision and law. (me)
|
|
|
Metacelsus
International Hazard
Posts: 2537
Registered: 26-12-2012
Location: Boston, MA
Member Is Offline
Mood: Double, double, toil and trouble
|
|
I have found microwaving to give inconsistent results with magnesium sulfate -- sometimes it doesn't remove all of the water, sometimes it does.
Sodium sulfate works fine, though.
|
|
|
quantumcorespacealchemyst
Banned Shitposter
Posts: 213
Registered: 17-10-2014
Member Is Offline
Mood: No Mood
|
|
powdering in mortar and pestle and heating in the kettle on moderate flame causes it to melt and puffletting out vapor and turning white gradually
till the mass is seemingly all white. the bottom of the cake formed seems to be possibly yellow and that may be due to impurities.
i had a solution of epsom salts used as a water bath in the same kettle that was let to crystallize and poured off the liquid to a cup and seperating
most of the mostly dry crystals to a bag, then i put the rest of the liquid logged crystals into the cup, i pipetted out the water that collected in
the plastic bag corners to the same cup, then the next night i believe, pipetted out the liquid from the cup to another cup, now having a mosly dry
bag of MgSO4, a cup of some and a cup of liquid which is yellowish. if the color isn't from the kettle, the cup, or dropping/spilling something in the
water bath (i believe it isn't these, especially the last) then it may impurities from the epsom salt.
the aforementioned dessication was done with non-recrystallized epsom salt
edit: i forgot to add, i am thinking of washing them with acetone, although the ones in the cup, i just washed with distilled water as they were
drying and i did not want to combine them with the first separation in the bag and/or have the impurities dry on the crystal surfaces. the crystals
lost some mass of course, quite a bit actually, estimating a third no a half (crude estimation).
 
[Edited on 12-12-2014 by quantumcorespacealchemyst]
[Edited on 12-12-2014 by quantumcorespacealchemyst]
[Edited on 12-12-2014 by quantumcorespacealchemyst]
|
|
|
unionised
International Hazard
Posts: 5109
Registered: 1-11-2003
Location: UK
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by CHRIS25 |
Well because after a few weeks I would have expected at the least, not to have been able to shake the 'powder' around so freely on the glass, plus I
used it as a desicant to absorb moisture from precipitated silicon dioxide when I put it into a homemade hot chamber - after one hour I became
suspicious, so I swapped this for sodium sulphate that I had made and within another 30 minutes the sodium sulphate was already half its volume with
moisture. |
OK, for a start you need to find the difference between hygroscopic (which MgSO4 is) and deliquescent (which it isn't).
Also, unless you dried it before you tried to use it as a drying agent it's simply not going to work.
|
|
|
aga
Forum Drunkard
Posts: 7030
Registered: 25-3-2014
Member Is Offline
|
|
You got CaCl2 dude.
Heat the hell out of it !
|
|
|
subsecret
Hazard to Others
Posts: 424
Registered: 8-6-2013
Location: NW SC, USA
Member Is Offline
Mood: Human Sadness - Julian Casablancas & the Voidz
|
|
It doesn't really matter if there's MgO in it, as long as you're drying with it. If you're using it as a reagent, there could be larger problems.
Fear is what you get when caution wasn't enough.
|
|
|
dermolotov
Hazard to Others
Posts: 114
Registered: 13-12-2014
Location: Toronto, Canada
Member Is Offline
Mood: Free
|
|
x2
I just use Calcium Chloride found at the local pool supply shoppe. They come in flakes similar to potassium hydroxide flakes which I bake in an oven
at 230deg for 30 minutes and they soak it up almost immediately. On top of the fact that it's much more inert, it's much cheaper, too.
|
|
|
![[*]](images/xpblue/default_icon.gif){kind=icon}
