N/P reducing pellets (solid vodka dosing)

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Generic, white vinegar. I bought it at Walgreens here, although I'm not sure what brand you would find in the Philippines.

I'm not sure if it would make a difference if you use rice wine vinegar, it is probably readily available there. There may be a few threads on vinegar dosing where you could read more.
 
I would suggest you start your own thread in this section(reef chemistry)
These posts are probably being overlooked by the chemistry experts as it is a very long specific thread

Thanks Capn... Just might do that although I would have thought my quere was related to any form of carbon dosing including np pellets. I was at one of the local fish stores yesterday and noticed similar behaviour. He was using a modest dose of np pellets, and the calc reactor was the more updated upward flow, so the melt was not streaking downward in the primary although there was a pile of calc residue at the bottom of the second pass-thru chamber...

I'll give it some more time, and if nobody bites, then perhaps I'll relocate the question as you've so keenly suggested.

Cheers,

Sheldon
 
Hi Scej 12 :) ,

-I'm not an calcium/alk reactor specialist (more a noob :) ) , because i dose my Ca and alk. with 2-channel dosing pump.

-But could it be that your media is covered and impregmented with bacteria , causing it to melt away by the extra provided CO2 from bacteria on a microscopic level , maybe not measured (Ph-wise) in the reactor water because the reaction is also inside the aragonite media??

---> if this would be the case , maybe installing a small UV-unit on the inlet hose of the reactor could do the trick;
No bacteria would enter the reactor chamber , so no bacteria there ?

Are you sure that the white sludge is not dead /alive bacteria ?
If it's sand-like it probably will not be the case and then it could be some sort of perticipation.

greetingzz tntneon :)
 
---> if this would be the case , maybe installing a small UV-unit on the inlet hose of the reactor could do the trick;
No bacteria would enter the reactor chamber , so no bacteria there ?



I have lots of bacteria clogging my gfo reactors from time to time ; hadn't thought of pre uv fitration ; might try it. Thanks.
 
Tom if you try that, let us know how it works out. My GFO reactor always gets clogged with detritus. I think a mechanical inline pre-filter would be better right?
 
I haven't jumped on board as of yet with the pellets so in the mean time been dosing vineager with kalk. Got the dry look on my acros. Not a pretty sight to say the least. Should be getting pettets in a week or so.........
 
Hi Scej 12 :) ,

-I'm not an calcium/alk reactor specialist (more a noob :) ) , because i dose my Ca and alk. with 2-channel dosing pump.

-But could it be that your media is covered and impregmented with bacteria , causing it to melt away by the extra provided CO2 from bacteria on a microscopic level , maybe not measured (Ph-wise) in the reactor water because the reaction is also inside the aragonite media??

---> if this would be the case , maybe installing a small UV-unit on the inlet hose of the reactor could do the trick;
No bacteria would enter the reactor chamber , so no bacteria there ?

Are you sure that the white sludge is not dead /alive bacteria ?
If it's sand-like it probably will not be the case and then it could be some sort of perticipation.

greetingzz tntneon :)

FWIW - I also think the solution will be to add a uv prefilter; as I really do think the behaviour is due to bacteria in the water column finding an intentional or unintentional home in the calc reactor. Your theory about the bacteria degrading the aragonite from within is an interesting one... I'm just not enough of a chemistry guy to be able to assess what exactly is happening... but as far as I can observe:
  • The reactor is maintaining some undissolved gas at the top (mostly due to the fact that it is not an upward flow reactor, however this is a definite change in function nonetheless);
  • Although my CO2 feed is definitely reduced, while media-melting is accelerated, the actual amount of CO2 dictates my achieved Ca and dKH levels no matter how much the media melts otherwise...

The above being the case; perhaps you are correct in that the residue could be some form of precipitate??? Perhaps PO4??? but that's a heck of a lot. And if so, why does the water within the reactor have such a reduced capacity to dissolve CO2 gas... or perhaps the gas dissolving capacity could be due to the water being occupied by some other forms of gas.. say N2??? What if, for argument sake, the bacteria is spending so much time within the CaCO3 reactor that it is dying off within; releasing it's P to precipitate with Calcium Phosphate or something of the like; and releasing it's N to form N2 gas at the top of the reactor... But then again, the media is definitely being reduced (lost about 3-4 inches in height over the past couple of months... this too is an acceleration of the norm)

I wish there was an easy way to test this stuff...:reading:

Thanks for throwing some thoughts into the mix.

Regards,

Sheldon
 
Tom if you try that, let us know how it works out. My GFO reactor always gets clogged with detritus. I think a mechanical inline pre-filter would be better right?

Don't know,It might just clog as well as the reactor will. A uv wouldn't help detritus but could reduce bacteria which is what grows in mine.
 
My question(s)

  1. How exactly does a Calcium reactor produce CO3: does fed-in CO2 associate w
  2. Does my above deduction make sense re: bacteria O2 consumption; CO2 production; and effect on CO3?
  3. ith O2 to produce CO3 thereby raising system carbonate hardness?
  4. If the answer to the first question above is affirmative; then what process allows bacterial activity to acidify the environment within the calcium reactor, while not registering any noticeable pH drop in the effluent from the second chamber... could this chamber (of aragonite) be actually buffering pH back up to overall system levels even though its media is also melting away albeit not as aggressively as the first chamber's media?
  5. What other possibilities could explain the above described phenomenon that have not been considered or described...???
I read your post 3885 and subsequent posts. I don't know precisely what's going on but organic carbon might be getting into the low flow pressurized reactor environment which could fuel heterotrophic bacterial activity there leading to increased dissolution of the media due to localized low ph.

The CO3 comes from the disassociation of calcium carbonate to calcium and carbonate at lower ph,ie more H+ whether from CO2 forming carbonic acid or another source like hydrogen sulfide, for example..
 

  • ....
  • Although my CO2 feed is definitely reduced, while media-melting is accelerated, the actual amount of CO2 dictates my achieved Ca and dKH levels no matter how much the media melts otherwise...

....

-Then i think this would be the evidence that it is some sort of precipitation , what mechanism i don't know....

Very intressting though , you could do some sort of a voting poll on how much " Ca-reactor combined with carbon dosing users" have the same issues you have.
I guess you will not be alone....

This definitly is a subject for guru's like Boomer and Randy if you ask me.

greetingzz tntneon :)
 
My question(s)
I read your post 3885 and subsequent posts. I don't know precisely what's going on but organic carbon might be getting into the low flow pressurized reactor environment which could fuel heterotrophic bacterial activity there leading to increased dissolution of the media due to localized low ph.

The CO3 comes from the disassociation of calcium carbonate to calcium and carbonate at lower ph,ie more H+ whether from CO2 forming carbonic acid or another source like hydrogen sulfide, for example..

Thanks for chiming in Tom. I would certainly bet that organic carbon is in deed getting into the reactor... What do you think the bacteria might be feeding on... the actual media...?? I was thinking this morning after responding to tntneon's post, that if the bacteria was in fact dying in the reactor wouldn't it be visible by brownish/blackish residue.. the reactor melt is completely white/calc. looking. I still can't seem to figure out why the pH is not below 7.9 - 8.1 within the reactor and all of that media is dissolving like crazy.. perhaps it is indeed heterotrophic activity doing the dissolving:uhoh3:

In any event - I believe I could easily figure out how to put a bandaid solution together to eliminate the symptoms but am nonetheless curious as to what actual mechanics are taking place to cause this carbon/bacterial based consequential effect. When I find the time, I might just opt to switch around the plumbing to a upward-flow arrangement; and add a settling area at the bottom of the pass-thru chamber. This way, both chambers will stay relatively clean (no streaking); and I will be able to resume a normal Ca and CO3 maintaining dose of CO2.

-Then i think this would be the evidence that it is some sort of precipitation , what mechanism i don't know....

Very intressting though , you could do some sort of a voting poll on how much " Ca-reactor combined with carbon dosing users" have the same issues you have.
I guess you will not be alone....

This definitly is a subject for guru's like Boomer and Randy if you ask me.

greetingzz tntneon :)

Thanks for the suggestions. Though I believe the effect is not as noticeable with the reverse-flow calc reactors with two chambers, unless you look specifically at the bottom of the second chamber.

I think I might have to lure Randy and Boomer to this question with a couple of pms...:twitch:

Regards,

Sheldon
 
Seems you could also use the by products of bacterial respiration and waste, eg fermentation(Vodka etc) and the other, particularly where O2 is low......acetic acid, which dissolved the CaCO3 quite well, it'll also lower dKH.

This could be tested also:

Use a small dosing pump to dose acetic acid, say 5% distilled and pH controlled via pH controller.

This could be used in place of CO2 and supply an organic reduced carbon source as well.

Cheaper and simpler than CO2 I would think.
 
hi scej12 ,

-Have you tryed to collect some of the "melt away"-substance , to exame it if it's sandy or not ?

a question that came to mind :

Isn't there a lower limit of PH in wich nitricificating bacteria thrive ?
I thought i somehere have read that the " nitrificing bacteria" die under a certain PH , don't know if it's true though....


greetingzz tntneon :)
 
Isn't there a lower limit of PH in wich nitricificating bacteria thrive ?

Not sure what it is;mot likely in the reactor though as these bacteria thrive in freshwater at much lower ph. However, denitrifying bacteria wane when they use up all the O2 and nitrate in the water at which point sufate reducing bacteria take over. They use the O from SO4(sulfate). This could easily occur in a reactor environment with low flow.
 
Quote:
<table width="100%" border="0" cellpadding="5" cellspacing="0"> <tbody><tr> <td class="alt2" style="border:1px inset"> Originally Posted by tmz
My question(s)
I read your post 3885 and subsequent posts. I don't know precisely what's going on but organic carbon might be getting into the low flow pressurized reactor environment which could fuel heterotrophic bacterial activity there leading to increased dissolution of the media due to localized low ph.

The CO3 comes from the disassociation of calcium carbonate to calcium and carbonate at lower ph,ie more H+ whether from CO2 forming carbonic acid or another source like hydrogen sulfide, for example..

</td> </tr> </tbody></table>
Thanks for chiming in Tom. I would certainly bet that organic carbon is in deed getting into the reactor... What do you think the bacteria might be feeding on... the actual media...?? I was thinking this morning after responding to tntneon's post, that if the bacteria was in fact dying in the reactor wouldn't it be visible by brownish/blackish residue..

I'd expect to see that too; but it does occur in sand beds on and off as evident in dissolution and some forms of clumping without apparent residue.
 
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