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Author: Subject: Thoughts On Anodes
quicksilver
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Dann2:

Again, thanks - your suggestions have consistently been valuable and appreciated.
dann2
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Hello,

Just when you though the subject of Cathodes was at an end........

http://www.faqs.org/patents/app/20080230381
which describes using Phosphates in conjunction with Fe-Mo alloy coated Cathodes for to buffer Chlorate electrolyte and stop Cathodic reduction thus eliminating Chromates.

ONLY HARD CORE, 'GREEN' CELL RUNNING FOLKS CAN GET INTO THIS STUFF
(I will be giving it a miss)

Dann2
ninefingers
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Quote: Originally posted by dann2
 Quote: Originally posted by ninefingers This is probably old hat to you guys, but: Ti anodes seem to corrode right at where they touch the air. That DMV can be painted and they will then work well. Even the copper rods I use to hold my anode and cathode get corroded, so I paint everything above the water level except exactly where I need electrical contact. That gets graphite grease.

 Quote: Can you explain what your "Ti Anodes" consist off?

They are pure titanium . Right where air contacts them they burn (DMZ, not DMV, sorry.) I'd still like to try gold filled chains before investing in Pt. I got ripped of by a Pt scam on eBay; there went my budget.

JohnWW
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 Quote: Originally posted by dann2 They are pure titanium . Right where air contacts them they burn (DMZ, not DMV, sorry.) I'd still like to try gold filled chains before investing in Pt. I got ripped of by a Pt scam on eBay; there went my budget.
Can you please tell us how the Pt $cam on eBay was operated? Who was the culprit? Gamal Harmless Posts: 24 Registered: 6-11-2005 Location: Sweden Member Is Offline Mood: No Mood  Quote: Originally posted by dann2 Hello, Just when you though the subject of Cathodes was at an end........ Link here: http://www.faqs.org/patents/app/20080230381 which describes using Phosphates in conjunction with Fe-Mo alloy coated Cathodes for to buffer Chlorate electrolyte and stop Cathodic reduction thus eliminating Chromates. ONLY HARD CORE, 'GREEN' CELL RUNNING FOLKS CAN GET INTO THIS STUFF (I will be giving it a miss) Dann2 Interesting reading! Looks like they use mmo-anodes with chromates in the electrolyte. I though that wasn't possible. Have I missed something? If I get it right, they get a ph stabilized cell only by the addition of phosfate to the cell. "The hypochlorite concentration was quickly stabilised at a value of 0.06 mol/l for the cell with activated cathodes, and of 0.07 mol/l for the cell with non-activated cathodes." Maybe I'm mixing things up here. /Gamal Gamal Harmless Posts: 24 Registered: 6-11-2005 Location: Sweden Member Is Offline Mood: No Mood Is this thread dead or what? This is my favourite thred for now, as I'm planning my cell configuration. I hope there will be some more interest in this topic in the future. I'm thinking about using an aquarium as the cell. Do you think it's a good idea? Does the silicon seals withstand the cell environment? /Gamal [Edited on 8-6-2010 by Gamal] hashashan National Hazard Posts: 255 Registered: 10-10-2006 Member Is Offline Mood: No Mood I noticed that in quite a short time all the adhesives degrade therefore my recommendation is to use a plain plastic container .. you can get those in quite large sizes so that it would fit you. hissingnoise International Hazard Posts: 3939 Registered: 26-12-2002 Member Is Offline Mood: Pulverulescent! I'd go for glass every time - a large glass jar; doesn't degrade or opacify over time. dann2 International Hazard Posts: 1523 Registered: 31-1-2007 Member Is Offline Mood: No Mood Na Perchlorate Hello Folks, It's been a while. I have have silicon sealer at the top of my cells and it does not seem to have degraded but it was NOT holding in any liqued. Just a seal to stop gases from getting out round the rim. If you just a want a small (2 liter cell) you can cut a glass 'demijohn' using a glass cutter and a hot wire to crack it. @Gamal. It is OK to use Chromated with MMO. Lead Dioxide does not like the stuff as it reduces CE. Some Sodium Perchlorate 'cakes' attached for you pleasure! The stuff is just about impossible to crystallize. I can't imagine how they do it in industry in a normal crystallizer (they probably do not). I heated the solution untill it just about all evaporated away and then drained off the small amount of solution that was left on cooling from the solid. I then vacuum filtered the stuff (Buchner funnel) and obtained the pictured cakes (wet hydrates of some description). I put the these cakes in an oven at 120 degrees C and they turned to pools of liquid. They dried eventually and the cakes were found to contain 22% water. Getting around to trying out a Bi doped Tin Oxide Anode for Perchlorate. Don't hold your breath. Dann2 mnick12 National Hazard Posts: 404 Registered: 30-12-2009 Location: In the lab w/ Dr. Evil Member Is Offline Mood: devious Good job on the perchlorate, what was your anode material? I have just been getting into chlorate synthesis and it is very neet. I am using a cobalt oxide/ nickel oxide with V2O5 on titanium for my anode and a iron cathode. I have had 3 cells so far two potassium chlorate and one sodium chlorate. The cells were powered by a cpu power supply. I have not weighed everything, but I would guess I have 700gr of KClO3 and mabe 300gr of NaClO3. The only trouble I have had is with the cathode corroding so I had to add about 200mg of CrO3, which seemed to stop it. The anode has not correded at all, so I hope some time try it in a perchlorate cell. Cool stuff though. I have been wondering what do most of you do with your chlorates and perchlorates? My pyro days are over so I have been using my chlorate as an oxidizer for some organic chemistry rections, like oxidizing hydroquinone to benzoquinone. But what do you guys use it for? thanks 12AX7 Post Harlot Posts: 4803 Registered: 8-3-2005 Location: oscillating Member Is Offline Mood: informative I have a bag (a few pounds) of what I expect is crude NaClO4. As I recall, the bag was leaky and humidity was getting in, causing it to turn to mush again. Last I checked, I double bagged it... The last thing I used chlorate for was speeding up the etching of circuit boards. I regularly use CuCl2 + HCl and it goes several times faster with chlorate. Be careful not to add too much or you'll gas yourself! Tim Seven Transistor Labs LLC http://seventransistorlabs.com/ Electronic Design, from Concept to Layout. Need engineering assistance? Drop me a message! Gamal Harmless Posts: 24 Registered: 6-11-2005 Location: Sweden Member Is Offline Mood: No Mood @12AX7 That's interesting! Do You use only chlorate or a mix of CuCl2 + chlorate? What concentrations do you use? It's nice to see this thread coming to live again! /Gamal 12AX7 Post Harlot Posts: 4803 Registered: 8-3-2005 Location: oscillating Member Is Offline Mood: informative I use a solution of bright green CuCl2 + HCl. There is probably a considerable amount of sodium in solution by now. Heat to about 50C, add NaClO3 periodically. More than a large pinch will result in chlorine fumes, which needless to say is unpleasant to the operator. Tim Seven Transistor Labs LLC http://seventransistorlabs.com/ Electronic Design, from Concept to Layout. Need engineering assistance? Drop me a message! white rabbit Harmless Posts: 33 Registered: 29-11-2009 Member Is Offline Mood: Groovy I have found that the platinum clad niobium electrodes from Anomet work exceptionally well. After well over a 1000 hours it appears unchanged. I use 304L stainless steel for the cathode and a rewound Mot for the supply. I run 25 amps at 6.2 volts measured at the electrodes. A run of 2.5 lbs KCl to chlorate takes 6 days to complete. 2.5lbs of NaCl to NaClO4 takes 180 hours minimum and complete conversion takes almost twice that. Solution temp runs a steady 85*C. The stainless cathode needs to be cleaned before every run. I do not adjust pH or run any chromates. Here is a pic of the anodes. Here is the stainless cathode with the section not in solution protected with heat shrink tubing Here, the direct conversion of KCl, is almost complete Here is the power supply. A rewound microwave transformer with a Pi filter. The secondary windings are 10 gauge and center tapped to use 2 diodes. There is 44,000Mfd on one side of the inductor and 85,000 on the other. Ripple is less than 1/10 volt at load. 980 grams KClO4 (1/2 of one run) Alexein Harmless Posts: 35 Registered: 14-7-2007 Member Is Offline Mood: Metastable Holy smokes! How much did those anodes cost you? and do they sell to individuals? hissingnoise International Hazard Posts: 3939 Registered: 26-12-2002 Member Is Offline Mood: Pulverulescent!  Quote: Originally posted by white rabbit I have found that the platinum clad niobium electrodes from Anomet work exceptionally well. After well over a 1000 hours it appears unchanged. Nice work white rabbit. . . The Pt plating on the anode will erode completely, though, given time. A way around this is to use a second Pt-plated electrode as a cathode. Pt lost from the anode will plate onto the cathode and this can be replated back by reversing the polarity of the cell every few hundred hours or so. As it is, Pt is plating onto the ST cathode and is lost when cleaning. I know it means double expense, but electrode life can be prolonged almost indefinitely. . . white rabbit Harmless Posts: 33 Registered: 29-11-2009 Member Is Offline Mood: Groovy @ Alexein/The electrodes were very reasonable, I think, at about$135 each including the shipping. I bought 4 for \$540. They save a great deal of time on filtering and washing.

Thanks,Hissingnoise
It seems if the anodes are going to eventually corrode I will probably be long dead by then. There is absolutely no sign of wear as of now. ( I've run of over 20 lbs so far)

I have tried the platinum cathode and I can tell you that it is a very bad thing to do. I completely destroyed, (turned to powder), one of the 4 electrodes I bought, which leads me to believe that your idea of the platinum plating onto the cathode in normal operation is incorrect. It seems the plating goes from negative to positive, this is why, it seems, my platinum cathode completely dissolved in about 150 hours. Have you noticed the extremely vigorous action at the cathode and almost no activity at the anode during the normal electrolysis? When I have finished a run of perchlorate, the cathode looks extremely corroded and the platinum looks just like new. I think the best combination is a Ti cathode and platinum anode. (the anodes are actually platinum clad niobium)

Btw,I have 6 videos on youtube of these electrolysis. Just search "ytmachx"
white rabbit
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Here is something that you probably don't come across too often.It appears to be a sodium chlorate crystal that I found in the bottom of my electrolyte one day.

[file]10743[/file]
12AX7
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Strange, I get differently shaped crystals, never cubic.

Tim

Seven Transistor Labs LLC http://seventransistorlabs.com/
Electronic Design, from Concept to Layout.
Need engineering assistance? Drop me a message!
hissingnoise
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 Quote: Originally posted by white rabbit I have tried the platinum cathode and I can tell you that it is a very bad thing to do. I completely destroyed, (turned to powder), one of the 4 electrodes I bought, which leads me to believe that your idea of the platinum plating onto the cathode in normal operation is incorrect. It seems the plating goes from negative to positive, this is why, it seems, my platinum cathode completely dissolved in about 150 hours. Have you noticed the extremely vigorous action at the cathode and almost no activity at the anode during the normal electrolysis?

For someone producing perchlorate by the pound you seem to know little about electrolysis. . .

12AX7
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I would think the large quantity of hydrogen would have a noticable effect on the cathode. Certainly it isn't plating across, and I find the theory suspect, that platinum will plate reversibly between anode and cathode. Foaming hydrogen is not conducive to bright, dense deposits.

Tim

Seven Transistor Labs LLC http://seventransistorlabs.com/
Electronic Design, from Concept to Layout.
Need engineering assistance? Drop me a message!
hissingnoise
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 Quote: Foaming hydrogen is not conducive to bright, dense deposits.

That would certainly be true in normal plating processes, but in this case the loss from the anode is really very small, so small that the rate of plating on the cathode would be so slow that effects from the evolution of H2 should be negligible. . .

white rabbit
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Quote: Originally posted by hissingnoise
 Quote: Originally posted by white rabbit I have tried the platinum cathode and I can tell you that it is a very bad thing to do. I completely destroyed, (turned to powder), one of the 4 electrodes I bought, which leads me to believe that your idea of the platinum plating onto the cathode in normal operation is incorrect. It seems the plating goes from negative to positive, this is why, it seems, my platinum cathode completely dissolved in about 150 hours. Have you noticed the extremely vigorous action at the cathode and almost no activity at the anode during the normal electrolysis?

For someone producing perchlorate by the pound you seem to know little about electrolysis. . .

You may have noticed, I do the work and then share the information, not just type theories. I may not have book smarts, but I have experience. I learned long ago, doing is better than talking and experience is a better teacher.

I've seen Tim's work and for that I have a great deal of respect for him.

Have you got anything to put on the table, or are you just going sit there and wiggle your fingers?

avi66
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if i run my sodium chloride cell with access sodium chloride on the bottom ... the access sodium chlorate will form pure crystal on the bottom in some stage?
i read that the crystallization of chlorate is selective ... so the crystals which i collect from the bottom of the cell are pure naclo3 which only need little surface purification?
if i use mno2 anode with non-controlled ph chlorate cell... i will not get hcl in the cell ... i get naoh ... so the anode corrosion will form only insoluble black mno2 powder?
hissingnoise
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 Quote: Originally posted by white rabbit As I have already stated, and proved, your theory is incorrect.

What?
My theory that metals from an electrolyte or anode plate onto the cathode of an electrolytic cell. . .
It's only the fundamental process in electrolysis - not a "theory"!
And you've now, already stated and proven that it is not correct?

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 Sciencemadness Discussion Board » Special topics » Technochemistry » Thoughts On Anodes Select A Forum Fundamentals   » Chemistry in General   » Organic Chemistry   » Reagents and Apparatus Acquisition   » Beginnings   » Responsible Practices   » Miscellaneous   » The Wiki Special topics   » Technochemistry   » Energetic Materials   » Biochemistry   » Radiochemistry   » Computational Models and Techniques   » Prepublication Non-chemistry   » Forum Matters   » Legal and Societal Issues