macckone
Dispenser of practical lab wisdom
Posts: 2168
Registered: 1-3-2013
Location: Over a mile high
Member Is Offline
Mood: Electrical
|
|
Filtering the impossible to filter: calcium sulfate and similar
This isn't exactly a beginner question.
More of a how do you do it question.
We have all had to deal with the almost impossible to filter precipiate of a double displacement with calcium sulfate as the waste product.
I have tried vaccum cleaner bags, nylons, even a french press.
Problems
1) a lot of liquid is entrained in the solid
2) the filter either lets through a lot of calcium sulfate or it clogs or both
so how do you deal with it?
I hate it is an acceptable answer.
|
|
karolus28
Hazard to Self
Posts: 51
Registered: 14-4-2019
Location: EU's Brazil
Member Is Offline
Mood: zgrzyt
|
|
I've heard of people putting "sand, coarse silica, alumina, even shredded paper" into the suspension and then filtering, not sure how it works.
Hi, please read about exif data.
|
|
B(a)P
International Hazard
Posts: 1139
Registered: 29-9-2019
Member Is Offline
Mood: Festive
|
|
I typically use standard filter paper and the biggest funnel I have. Then it is down to the passage of a lot of time and the acceptance that I will
loose yield because as you point out a lot of liquid remains entrained in the solid. Vacuum filtration with a buchner in my experience takes only
slightly less time if you have a lot of very fine solid material and I don't like running my pump for extended periods. Decanting off as much liquid
as possible after the solid has settled for a period of time (sometimes days) is generally the best way to go IMHO. If I am not concerned about yield
I will often not even bother with the remaining liquid and solid after initial decanting.
I have tried the following, but with little success:
- using a kitchen sieve lined with paper towel to try and increasing filtration surface area.
- making vessels from inverted 2 L milk containers with holes in an inverted screwed on lid lined with filter paper. The idea here was to build up
some head to drive the liquid through.
Great topic! I look forward to hearing the solution to removing barium sulfate from acids that attack organic material while preserving yield.
|
|
Rainwater
National Hazard
Posts: 919
Registered: 22-12-2021
Member Is Offline
Mood: indisposition to activity
|
|
In industry, a belt filter is used in combination with heat. Basicly providing unlimited surface area
"You can't do that" - challenge accepted
|
|
UC235
National Hazard
Posts: 565
Registered: 28-12-2014
Member Is Offline
Mood: No Mood
|
|
Add a whole bunch of celite/diatomaceous earth (acid washed if maintaining pH is important. The cheap (pool) stuff is alkaline). Flip initial filtrate
until clear. Wash cake out thoroughly.
Mostly I filter lots of horrible sticky, tarry protein glop.
[Edited on 27-8-2022 by UC235]
|
|
PirateDocBrown
National Hazard
Posts: 570
Registered: 27-11-2016
Location: Minnesota
Member Is Offline
Mood: No Mood
|
|
Start out with as dilute solutions as is practical.
Phlogiston manufacturer/supplier.
For all your phlogiston needs.
|
|
draculic acid69
International Hazard
Posts: 1371
Registered: 2-8-2018
Member Is Offline
|
|
This may or may not help but a cotton t-shirt (preferably white) can act as a quick coarse filter if solution is not too far from neutral pH and it
can be twisted and squished to recover solutions
[Edited on 27-8-2022 by draculic acid69]
|
|
Metacelsus
International Hazard
Posts: 2539
Registered: 26-12-2012
Location: Boston, MA
Member Is Offline
Mood: Double, double, toil and trouble
|
|
Perhaps you could centrifuge instead of filtering?
|
|
Gammatron
Hazard to Others
Posts: 125
Registered: 30-8-2022
Location: Abandoned Uranium Mines
Member Is Offline
|
|
I wonder if you could use a large sep funnel. Since the particles are so small and always remain somewhat suspended even after settling I don't expect
it would clog. I've also had success using a pump or siphon too.
|
|
WGTR
National Hazard
Posts: 971
Registered: 29-9-2013
Location: Online
Member Is Offline
Mood: Outline
|
|
When I made graphene oxide (this is completely impossible to bulk filter), I loaded the suspended samples into dialysis tubing and stirred them for
several days in a large beaker until the rinse water was neutral. I did the same thing when successfully producing amorphous titania, that did not
separate out in the centrifuge even.
Of course, that was when I was trying to keep the precipitate, not discard it…but a little DE does help on filter paper in those cases. A little is
just enough. A bit more is way too much.
The counterintuitive thing is that fine particles will clog coarse filter paper. For fine precipitates you need the finest filter paper. Things
like a thin layer of DE keeps these fine particles from getting into the pores of the filter.
[Edited on 22-09-02 by WGTR]
|
|