Science Forums: Potassium Hydroxide Separation - Science Forums

Jump to content

Welcome to ScienceForums.Net!

Welcome to ScienceForums.Net! We welcome science discussion at all levels — from beginners to researchers, covering topics from biology to computer science, and much more. Registration is fast and free, and allows you to post on the forums, so register now and join the discussions!
  
After you've registered, come in and introduce yourself, or visit the forum index. If you need any help  registering, posting, or if you just have some questions about our site, please feel free to contact us at staff at scienceforums dot net.

  • Start new topics and reply to others
  • Subscribe to topics and forums to get automatic updates
  • Create a ScienceForums.Net Blog!
Guest Message © 2012 DevFuse
  • 2 Pages +
  • 1
  • 2
  • You cannot start a new topic
  • You cannot reply to this topic

Potassium Hydroxide Separation Rate Topic: -----

#21 Suxamethonium 


Baryon
The point of it is that more can dissolve once the sulfate or carbonate precipitates- thats why it is included as a solid and 'washed' with water. That is also why I proposed my initial procedure to try- its the same principle without the ash (using readily available suflate instead)- I still think its worth a try but its up to you. Kudos if you can be arsed to get the clippings and burn them.

Edit- sentence structure.

This post has been edited by Suxamethonium: 5 March 2012 - 02:14 PM

0

#22 John Cuthber 


Icon
Chemistry Expert

View Postelementcollector1, on 1 March 2012 - 04:19 AM, said:

Still, 0.173 is rather small. What about electrolysis? Or is there a more soluble hydroxide that converts to an insoluble carbonate?

http://en.wikipedia....arium_hydroxide
does better but it's rather toxic and much more difficult to get hold of.
What's this signature thingy then? Did you know Santa only brings presents to people who click the + sign? -->
0

#23 elementcollector1 


Baryon

View PostJohn Cuthber, on 5 March 2012 - 07:09 PM, said:

http://en.wikipedia....arium_hydroxide
does better but it's rather toxic and much more difficult to get hold of.


Luckily for me, I have a baryte rose I can convert if necessary, but not a lot.
So, I think electrolysis is still the best route here (no possible contaminants except for K2CO3). So, what is the best setup for this? I have a 12V plug-in adapter for electricity (does that convert amps as well?) Should I use carbon electrodes (taken from zinc-carbon batteries, I also have titanium if necessary)? What kind of apparatus should I use? I've heard that I should use two beakers with a saltwater-soaked tissue between them, and a saturated solution of KCl in each. Is there a better way to maintain electron flow between the two half-cells (gold wire)?
Sorry for the barrage of questions, I've tried electrolysis of KCl before with not-so-good results (9V battery source).


EDIT: Trying this with a 6V cell (made of 4 of those fat Duracell's), gold anode, graphite cathode (14k gold corroded), and an aqueous solution of NaCl. Will measure pH when the thing stops bubbling.

This post has been edited by elementcollector1: 5 March 2012 - 11:38 PM

0

Share this topic:


  • 2 Pages +
  • 1
  • 2
  • You cannot start a new topic
  • You cannot reply to this topic

1 User(s) are reading this topic
0 members, 1 guests, 0 anonymous users