New Skimmer – Price is no Object!

I'm not missing the point at all. Almost everything I see that keeps getting repeated about protein skimmer contact times, interface, whatever is a large degree of speculation with little if any scientific fact behind it.
 
Holmes-Farley pointed out the unlikely science behind Escobal's model. Its not like a bubble is going to be travelling side by side with a protein for 2 minutes before it is finally attracted. There are other forces at play. This is where things get messy.

Randy's model suggests that a bubble attracts proteins, and as the bubble 'dwells' longer, more hydrophobic proteins replace less hydrophobic substances... so in effect, the lesser proteins lose their spot, and have to wait for another bubble.

This is where my interpretation comes in, so take it for what its worth. Okay, so on a shorter skimmer, its a bit like the 'soapy water bubble' analogy... not enough soap in the water, and your bubbles just pop. Since its not like our tanks are laden with skimmate or raw sewage, our 'soapy water' is very weak. On shorter skimmers, very turbulent ones, etc... the bubbles may not attract enough proteins in a low-DOC environment to become stable enough to be collected in the cup. ATI's, for instance, cant skim much more than yellow water when the tank they are put on doesnt have enough protein production (need more anthias!) for the bubbles to collect as they get flung from the bottom to the top of the skimmer. In some cases, where we like to put oversized 500g rated skimmers on 150g tanks (habit from past makers who had inflated claims), the skimmer just doesnt work anymore. Yet somehow, a taller skimmer can. It it that the taller skimmer just allows the bubble to 'build up' a better shell under low DOC conditions? Or, is the taller skimmer just able to attract proteins that the shorter skimmer doesnt have the opportunity to collect at all? I wish I knew. According th Randy, I think he would side with the first example though... as his model pretty much says that the taller the skimmer, the more hydrophobic the proteins will be built up on the bubble. Escobal hints that 'rarer' or harder to collect proteins might need the time. Either way... both examples would seem to agree that a taller skimmer would be better, esp in lower DOC conditions. Sure, the counter to more height would be more air, but if all the bubbles just pop when you hit the neck... what good is that? To skim the harder to get proteins, you would in effect have to add more of the easy ones to create a stable head so both can be taken out.

This is why I started experimenting with vodka dosing on my low DOC system. Im encouraging the nutrient uptake by bacteria, and producing more 'substance' for my skimmer to work with.

Other things I will point out though... this would be the major argument for recirculating vs. single pass skimmers. IF height isnt available, and there are certain 'harder to get' proteins in the water... then keeping the water in the skimmer longer would seem to be a good response. Rather than continuing to pass it throught he skimmer too fast for anything to be collected time after time... slow it down, and let the water get 'scrubbed' harder.

Also, the longer the water stays in the skimmer... the more the ORP is buffered, and the pH raised. Now, we have all noticed on our systems how certain times of the day (usually night) seem to make more of a difference with skimming. So the prolonged exposure could be responsible for some chemical 'restructuring'... chemicals that otherwise wouldnt be skimmed might now be skimmable due to the chemical change of a longer time being blasted with bubbles.

As to what 2 minutes really means... who knows. It could mean that even with a very short skimmer, leaving the water in for that long (so a water exposure time) would be ideal to get out more 'stubborn' substances... Randy might side with that more. Or, could it be bubble dwell time? Well... Randy pointed out that its not like the protein and bubble are side by side the whole time... its an instant attraction, and if things stick thats it. Its not like the protein is going to be 'nearby' for 120 seconds and then 'make up its mind'. My interpretation would be that some DOC's just need to be in contact with the bubble for that long before they have a strong enough contact bond to go throught the collection process in the neck, drainage, turbulence, other bubbles, etc... and make it into the cup. OR, as Randy suggests, perhaps its that with longer dwell times we are actually just getting more of the easier to get proteins onto the bubbles so they are more able to be collected... not the more stubborn ones.

This would explain becketts somewhat. Short dwell time, but rather than trying to make the most stable bubbles, the beckett just tries to collect as much as it can and put it into a column of water.... a tall and narrow column without waterflow... just a huge head of foam. This huge head of foam drains like normal, but its production rate of foam is higher than the bubbles can pop... so proteins that get stuck in the head have a hard time draining out. Speculation 100%, but educated guess based on various theories. Rather than trying to maximize the dwell time under the water, try to maximise the dwell time in the foam head... adding more bubbles faster than they can drain.

Either way you look at it, thats why I say, they all pretty much agree on one thing. It may be overkill, but the best skimmer would be one with not only decent air throughput, but a decent height as well, and a recirculating/counter-current design.

I would add that the cone might be a way to get needlewheel skimmers to behave more like becketts... a large sorting area at the bottom with the large part of the cone (or 'black box'), yet a tall and narrow head up top for keeping a high bubble concentration in a small area up top, like that 'black box' has when you put a 5" cylinder at its top. A skimmer with a 8" diameter base has a hard time keeping that kind of bubble density at the top like a beckett without a reducer very low on the skimmer, as the top is also 8" in diameter. A narrower cylinder can make sorting too hard, and so a smaller pump is used... so next to a big fat box at the bottom of the skimmer, and a low transition to the reducer, the cone may be the next best thing. And then you get the nice smooth transition from bottom to top that wont disrupt bubbles on the way up. Thats why I want to try out the ATB cone skimmers... it will fill in some questions I have about skimmers in general.
 
Water Dwell Time vrs. Air Dwell Time

Water Dwell Time vrs. Air Dwell Time

Thanks Hahnmeister and Sherm71Tank.

For those interested, here's ChemE's post regarding the distinction between water dwell time and air dwell time. It is from the "Skimmer Principles" thread in the Advanced Topics forum. Whether or not we agree with him, it is important to understand the distinction.
<a href=showthread.php?s=&postid=5937462#post5937462 target=_blank>Originally posted</a> by ChemE
To explain the difference between water dwell time and air dwell time reread my post on the first page; it was long winded but I thought thorough. I'll summarize here.

The protein will remain captured by the bulk fluid until it embeds in the bubble wall. This process can take up to 120 seconds. Allow me the use of an analogy that might make things clearer...

I have terribly slow reactions, so much so that it takes me 120 seconds to catch a basketball thrown at me. Throwing millions of basketballs at me very quickly will not help me catch even one. What you need to do is throw the basketballs extremely slowly, so that they take 120 seconds to pass near to me thus giving my slow reflexes time to kick in and catch it. Now, it is impractical/impossible to throw things this slowly since gravity makes them move faster than that so we'll throw me too. If you throw me at the same speed as the ball, then I get my 120 seconds next to one ball and am able to catch it.

It is the same way with bubbles and proteins in the water. It doesn't do us any good to pelt a protein with a cloud of fine bubbles because it doesn't spend enough time next to ONE of them. Sure, it might get pelted for 120 seconds before it exits the skimmer but that is not how embedding works, it needs 120 seconds next to the SAME bubble to embed. If it is in contact with one bubble for 2 seconds and then it moves away and is in contact with a new bubble the embedding process must by definition start all over. 60 such restarts before exiting the skimmer will produce no result (at least not the one I want).

I think bombardment rate is a load of crap unless I completely misunderstand it (possible).

The only thing that makes any sense whatsoever is one bubble being in contact with one protein for long enough that that hydrophobic portion of the protein moves inside the air/water interface and becomes captured by the air bubble. This increases the surface tension of the air bubble and if this surface tension is increased enough, it will not pop until it is in the skimmer collection cup. Then and only then is a protein removed from the system.
 
Wow.. you guys are still posting in this thread??

It has made NO progress since day one. You are all just running around in circles.....
 
<a href=showthread.php?s=&postid=10700016#post10700016 target=_blank>Originally posted</a> by ralphie16
LOL, ......... those crazy Krauts use to describe the yellow water.......

Hi Ralphie..
nobody use the name : .. Gelbstoff... :confused: in Germany... the Krauts are using best skimmers and make many waterchange...:D :D Nobody in Germany now Gelbstoff...:D :D :D

regards. Klaus
 
<a href=showthread.php?s=&postid=10701152#post10701152 target=_blank>Originally posted</a> by hahnmeister
Holmes-Farley pointed out the unlikely science behind Escobal's model. Its not like a bubble is going to be travelling side by side with a protein for 2 minutes before it is finally attracted. There are other forces at play. This is where things get messy.

Randy's model suggests that a bubble attracts proteins, and as the bubble 'dwells' longer, more hydrophobic proteins replace less hydrophobic substances... so in effect, the lesser proteins lose their spot, and have to wait for another bubble.

This is where my interpretation comes in, so take it for what its worth. Okay, so on a shorter skimmer, its a bit like the 'soapy water bubble' analogy... not enough soap in the water, and your bubbles just pop. Since its not like our tanks are laden with skimmate or raw sewage, our 'soapy water' is very weak. On shorter skimmers, very turbulent ones, etc... the bubbles may not attract enough proteins in a low-DOC environment to become stable enough to be collected in the cup. ATI's, for instance, cant skim much more than yellow water when the tank they are put on doesnt have enough protein production (need more anthias!) for the bubbles to collect as they get flung from the bottom to the top of the skimmer. In some cases, where we like to put oversized 500g rated skimmers on 150g tanks (habit from past makers who had inflated claims), the skimmer just doesnt work anymore. Yet somehow, a taller skimmer can. It it that the taller skimmer just allows the bubble to 'build up' a better shell under low DOC conditions? Or, is the taller skimmer just able to attract proteins that the shorter skimmer doesnt have the opportunity to collect at all? I wish I knew. According th Randy, I think he would side with the first example though... as his model pretty much says that the taller the skimmer, the more hydrophobic the proteins will be built up on the bubble. Escobal hints that 'rarer' or harder to collect proteins might need the time. Either way... both examples would seem to agree that a taller skimmer would be better, esp in lower DOC conditions. Sure, the counter to more height would be more air, but if all the bubbles just pop when you hit the neck... what good is that? To skim the harder to get proteins, you would in effect have to add more of the easy ones to create a stable head so both can be taken out.

This is why I started experimenting with vodka dosing on my low DOC system. Im encouraging the nutrient uptake by bacteria, and producing more 'substance' for my skimmer to work with.

Other things I will point out though... this would be the major argument for recirculating vs. single pass skimmers. IF height isnt available, and there are certain 'harder to get' proteins in the water... then keeping the water in the skimmer longer would seem to be a good response. Rather than continuing to pass it throught he skimmer too fast for anything to be collected time after time... slow it down, and let the water get 'scrubbed' harder.

Also, the longer the water stays in the skimmer... the more the ORP is buffered, and the pH raised. Now, we have all noticed on our systems how certain times of the day (usually night) seem to make more of a difference with skimming. So the prolonged exposure could be responsible for some chemical 'restructuring'... chemicals that otherwise wouldnt be skimmed might now be skimmable due to the chemical change of a longer time being blasted with bubbles.

As to what 2 minutes really means... who knows. It could mean that even with a very short skimmer, leaving the water in for that long (so a water exposure time) would be ideal to get out more 'stubborn' substances... Randy might side with that more. Or, could it be bubble dwell time? Well... Randy pointed out that its not like the protein and bubble are side by side the whole time... its an instant attraction, and if things stick thats it. Its not like the protein is going to be 'nearby' for 120 seconds and then 'make up its mind'. My interpretation would be that some DOC's just need to be in contact with the bubble for that long before they have a strong enough contact bond to go throught the collection process in the neck, drainage, turbulence, other bubbles, etc... and make it into the cup. OR, as Randy suggests, perhaps its that with longer dwell times we are actually just getting more of the easier to get proteins onto the bubbles so they are more able to be collected... not the more stubborn ones.

This would explain becketts somewhat. Short dwell time, but rather than trying to make the most stable bubbles, the beckett just tries to collect as much as it can and put it into a column of water.... a tall and narrow column without waterflow... just a huge head of foam. This huge head of foam drains like normal, but its production rate of foam is higher than the bubbles can pop... so proteins that get stuck in the head have a hard time draining out. Speculation 100%, but educated guess based on various theories. Rather than trying to maximize the dwell time under the water, try to maximise the dwell time in the foam head... adding more bubbles faster than they can drain.

Either way you look at it, thats why I say, they all pretty much agree on one thing. It may be overkill, but the best skimmer would be one with not only decent air throughput, but a decent height as well, and a recirculating/counter-current design.

I would add that the cone might be a way to get needlewheel skimmers to behave more like becketts... a large sorting area at the bottom with the large part of the cone (or 'black box'), yet a tall and narrow head up top for keeping a high bubble concentration in a small area up top, like that 'black box' has when you put a 5" cylinder at its top. A skimmer with a 8" diameter base has a hard time keeping that kind of bubble density at the top like a beckett without a reducer very low on the skimmer, as the top is also 8" in diameter. A narrower cylinder can make sorting too hard, and so a smaller pump is used... so next to a big fat box at the bottom of the skimmer, and a low transition to the reducer, the cone may be the next best thing. And then you get the nice smooth transition from bottom to top that wont disrupt bubbles on the way up. Thats why I want to try out the ATB cone skimmers... it will fill in some questions I have about skimmers in general.


Great summary Hahn! I agree that the extra "scrubbing" in recirc skimmers is makes them more efficient than single pass but the amount of air and foam column are also important. Thats why I still use a Beckett and I found recirc Becketts to be counter productive in my tests. I will be trying a DAS-EX2 soon and hope I like it.
 
<a href=showthread.php?s=&postid=10701313#post10701313 target=_blank>Originally posted</a> by jimdogg187
Wow.. you guys are still posting in this thread??

It has made NO progress since day one. You are all just running around in circles.....
If there is no progress in threads such as this one, then ignorant aquarists are being ripped off by uninformed purchasing of expensive skimmers that do not enhance water quality.

"A fool and his money are soon parted."
 
Re: Remora in Cesspool vrs. Bubble King in Waikiki Aquarium

Re: Remora in Cesspool vrs. Bubble King in Waikiki Aquarium

<a href=showthread.php?s=&postid=10666291#post10666291 target=_blank>Originally posted</a> by pjf
...., here is an article comparing a downdraft skimmer to a counter-current skimmer by Richard Harker: http://www.tsunamiaquatic.com/page/page/1790661.htm.

@pjf...
good idea..... we want building al clone : Bubble King without Pump and downdraft....

regards.... Klaus
 
<a href=showthread.php?s=&postid=10701380#post10701380 target=_blank>Originally posted</a> by pjf
If there is no progress in threads such as this one, then ignorant aquarists are being ripped off by uninformed purchasing of expensive skimmers that do not enhance water quality.

"A fool and his money are soon parted."

I love these types of threads. Asking tough questions is the only way to get real answers. While I don't consider myself a fool, I've certainly parted with a good deal of money in this hobby. I'm sure a few $K in the way of skimmers through the years.
 
Re: Re: Remora in Cesspool vrs. Bubble King in Waikiki Aquarium

Re: Re: Remora in Cesspool vrs. Bubble King in Waikiki Aquarium

<a href=showthread.php?s=&postid=10701449#post10701449 target=_blank>Originally posted</a> by Klaus Jansen
@pjf...
good idea..... we want building al clone : Bubble King without Pump and downdraft....

regards.... Klaus

Hello Klaus, nice to see we might have grabbed your interest. Not sure what you mean by 'al clone', or 'Bubbleking w/o pump & downdraft...."

From ChemE's quote: "it needs 120 seconds next to the SAME bubble to embed"

I tend to agree with this. It complies with both Randy's version, and the earlier Escobal.
 
<a href=showthread.php?s=&postid=10700622#post10700622 target=_blank>Originally posted</a> by sherm71tank
I'm not missing the point at all. Almost everything I see that keeps getting repeated about protein skimmer contact times, interface, whatever is a large degree of speculation with little if any scientific fact behind it.

Sherm... my comments were very cleary directed at the response from PJF. I quoted that response in my post.
 
Maybe the better question is what is making the water yellow in the first place. I personally do not have that problem, nor do I see it in local reef club members tanks. I dont feel uniformed or ripped off by my expensive skimmer, the skimmate I dump out is plenty of proof to me that my water quality is enhanced.

If you water is yellow run some carbon, if your phosphates are out of whack run phosban, if you ph is low use kalk, etc. Might as well blame high end skimmer manufacturers for any other problems if you follow the logic.
 
<a href=showthread.php?s=&postid=10702787#post10702787 target=_blank>Originally posted</a> by BeanAnimal
Sherm... my comments were very cleary directed at the response from PJF. I quoted that response in my post.

Sorry about that. :(
 
Thats actually pretty well described by many biologists. I think it pretty much comes down to any organics that are left in the water long enough for the aerobic bacteria to convert. The process of the conversion to nitrate is what produces the 'yellow' as well as phosphates (byproducts). There are other things as well though. Algae, macro algae, etc... all these things contribute to yellowing the water in one way or another... but being that there are many proteins that a skimmer doesnt even have a chance of collecting, it would seem that yellowing of the water is something that cant be avoided. So all you can do is deal with it... ozone and carbon... oh, and water changes. Oh, and Im sure there are some zeovit/prodobio/ultralith products out there for dealing with yellow water as well. Vodka dosing included.
 
<a href=showthread.php?s=&postid=10702955#post10702955 target=_blank>Originally posted</a> by hahnmeister
Thats actually pretty well described by many biologists. I think it pretty much comes down to any organics that are left in the water long enough for the aerobic bacteria to convert. The process of the conversion to nitrate is what produces the 'yellow' as well as phosphates (byproducts). There are other things as well though. Algae, macro algae, etc... all these things contribute to yellowing the water in one way or another... but being that there are many proteins that a skimmer doesnt even have a chance of collecting, it would seem that yellowing of the water is something that cant be avoided. So all you can do is deal with it... ozone and carbon... oh, and water changes. Oh, and Im sure there are some zeovit/prodobio/ultralith products out there for dealing with yellow water as well. Vodka dosing included.

Don't forget sugar. (Not me, the sweetener!)
 
No problem sherm... just wanted to make sure that you were growling at the right person :)

This has been fun guys... but honestly, I have better things to do (like empty the skimmer cup).

When you get it figured out and start selling tests and a skimmer that performs better than the other stuff out there.. let me know. :)
 
<a href=showthread.php?s=&postid=10702787#post10702787 target=_blank>Originally posted</a> by BeanAnimal
Sherm... my comments were very cleary directed at the response from PJF. I quoted that response in my post.
And I answered you by citing ChemE's post. Goodbye.

No need to apologize to anyone, Sherm. Your comments are very much appreciated. Thank you.
 
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Welcome, Klaus!

Welcome, Klaus!

To recap, this thread started with a request for information leading to a skimmer that can skim Gelbstoff or yellowing compounds, normally removed by carbon filtration. Some aquarists believed that tall counter-current skimmers of yore used to skim Gelbstoff but no one can find a current skimmer that can.

Now, yellowing compounds are simply proteins with greater solubility than surface proteins. Skimmers are great at removing surface proteins but not proteins that dissolve more readily in water. The thread starter then asked for skimmers that can skim proteins with higher solubility constants. Unfortunately, no one actually knew how much proteins or dissolved organic compounds (DOC) remained in their aquariums after skimming.

An alternative suggestion was offered to choose the skimmer that collects the most skimmate. This suggestion was discarded because:

• There is no cheap and easy way to compare the amount of organics in wet skimmate and dry skimmate.
• Two skimmers may collect skimmate at the same rate but one can leave more organics in the aquarium because it requires a higher concentration of organics before it starts skimming. A Remora in a cesspool can collect more skimmate than a Bubble King in the Waikiki Aquarium.

The consensus is that aquarium water purity is a better indicator of skimmer performance than observation of the collection cup. Ideally, skimmers should be measured by their ability to remove a protein, such as Gelbstoff, that can be seen. Since most dissolved organic compounds are colorless, a test must be developed. The Salifert Organics Test Kit was deemed to be too low in resolution. Ultraviolet spectrophotometers (280nm wavelength) were deemed to be too expensive for general use.

The thread is moving on to discuss skimmer theory and the best way to remove proteins that are more soluble than the easy-to-skim surface proteins. Pedro Escobal’s (Aquatic Systems Engineering: Devices and How They Function) observation that some proteins require 2 minutes of dwell time for bubble attachment was cited.

The esteemed Klaus Jansen, inventor of the Bubble King, honored all of us by joining the thread to offer his comments!
 
<a href=showthread.php?s=&postid=10703421#post10703421 target=_blank>Originally posted</a> by pjf
And I answered you by citing ChemE's post. Goodbye.
No need to apologize, Sherm.

The apology was to me PJF, not to you... so why answer like that? Must you always try and throw a little jab into everything? Honestly man, it gets rather old.
 
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"Since most dissolved organic compounds are colorless, a test must be developed. The Salifert Organics Test Kit was deemed to be too low in resolution. Ultraviolet spectrophotometers (280nm wavelength) were deemed to be too expensive for general use."

Just a stab in the dark here, but has anyone considered petitioning a laboratory that already has the equipment to run the analysis. Would be tons cheaper, still not cheap though. This kind of equipment may even be available on some college campuses. Considering the number of students we have in this hobby, might be worth a try (I'm not volunteering though :P)
 
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