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Thread: Algae, TA or what?

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    Default Algae, TA or what?

    couple o' things:
    first, what kind of pool do you have? If it is plaster how old is it? Are you only using bleach for chlorination?

    Second, drop the TA a bit more, ti will help

    Do you have any water features? Aeration will speed pH rise.
    When you add acid to lower the pH how low do you go? The lower the pH the faster it rises. Try not to lower it below about 7.6

    If you still have algae the answer is simple, you need more chlorine. Bump tiup to about 6-7 ppm. How much chlorine loss do you have daily. Hot climates like Arizona and Florida often do better with higher CYA in water. If you are having a problem maintaining FC (which your algae problem indicates) then try bumping up the CYA to around 50 or even higher. 80 is not too high in a hot climate that gets a lot of sun. Just adjust your FC levels accordingly and you are good to go.
    Retired pool store and commercial pool maintenance guy.

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    Default Re: any way to control pH better?

    I would go further and say if you have algae, you should START by adding sufficient chlorine to achieve the recommend shock level--that's FC of 15ppm, and keep it there at least 24 hours after your algae is all gone.

    I wouldn't mess with anything else other than lowering your pH to 7.5/7.6 until the algae is gone. With the high FC reading, though you'll get a higher pH reading than you'd like. As long as it's in the 7's you're OK, but keep the FC up there!

    I'm of the firm opinion that algae means you need to raise FC to shock level and anything else is just asking for trouble.

    Don't worry about CYA, TA, Borates, rising pH or anything else till it's cleared up.
    Carl

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    Default Re: Algae, TA or what?

    Hey Guys;

    I'm missing some things here.

    Waterbear, I'm not clear on your thinking about TA. You may have some really good reasons behind your thinking, but right now, I'm kinda puzzled. Do you have reason to think that lowering Alk will reduced acid demand or pH rise? Have you seen evidence that a really low Alk (below say 50 ppm) is OK for a plaster pool? Why did you feel that lowering Alk was more important than dealing with her algae?


    CarlD, are you aware that chlorine becomes less effective against algae as pH increases? The most dramatic problems are with unstabilized chlorine, but as best I can make out, the problem is still significant in stabilized pools, too. Since she reported that her pH was tending to go ABOVE 8, it's my opinion that that's an issue that needs to be addressed in the short term, in addition to raising the chlorine.


    Chem Geek has done some stuff with 'carbonics' that I haven't had a chance to digest, or much less fully consider yet. However even once I do, I'm not prepared to toss out all S.I. considerations without some experimental verification first. Stoichiometry is nice, and successful process chemistry often resembles the stoichiometric analysis, but rarely is identical with it.


    I'm leaning toward stating some 'standard' recommendations for Pool Forum responses, but I'd like to see what y'all have to say, first.

    As always, thanks for all your help.

    Ben
    "PoolDoc"
    Last edited by PoolDoc; 07-08-2010 at 09:47 AM.

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    Default Re: Algae, TA or what?

    Ben,

    Yes I'm aware that lower pH makes chlorine more effective at sanitation. But I'm also concerned that at high FC levels, the pH test can appear higher than it is. Adding extra drops of 0007 can compensate, but 0007 itself affects pH, too, correct? I've forgotten whether it's acidic or basic.

    So, given that, I took that leap that if someone's FC is 15, a pH in the 7's is probably OK (since the CYA is moderate).

    Carl
    Carl

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    Default Re: Algae, TA or what?

    This post is the one showing the difference in active chlorine (hypochlorous acid) level as the pH varies with no CYA and with CYA. The main point is that though it varies much more when there is no CYA, the absolute level is much higher with no CYA so it all depends what you are comparing against. If you compare no CYA against no CYA, then the pH is a big factor.

    Even so, if you shock with a lot of chlorine, especially 15 ppm or more, then it's a good idea to lower the pH to 7.2 (or even lower if you are shocking to even higher levels) because the addition of chlorine will raise the pH substantially, even beyond 8.0. Yes, when the chlorine gets used up the pH will mostly come back down but shocking is a sustained high level of chlorine so would be a sustained high pH if you don't lower the pH first.

    For a shock of 10 ppm, adjusting the pH isn't that important if it's starting out around 7.5 or so.

    As for TA, there was a forum user who found that his pH would rise over time a lot but that when the TA went down to 50 or 40 ppm the pH became stable. It was an extreme case, but we see this a lot in spas (at poolspaforum.com) due to the higher aeration (assuming they are using bleach and not Dichlor, except initially). There are many SWG pools that have lower pH rise at lower TA levels as well. However, in most pools 70 or 80 ppm is OK. A lower TA should be perfectly fine IF one adjusts their target TA and Calcium Hardness (CH) to keep the saturation index near zero. No one is saying to ignore the saturation index if one has a plaster (or fiberglass) pool.
    Last edited by chem geek; 07-08-2010 at 08:22 PM.

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    Default Re: Algae, TA or what?

    Ben,

    Regarding this post, I want to comment on some of the things that you wrote which I'll quote below.

    I can observe that, in my experience with multiple large commercial pools managed with sodium hypochlorite (bleach) feed systems, I universally found that bleach fed pools 'wanted' to be at a pH of 7.6 or higher. I have no analytical explanation for this. But I can tell you that I discovered that if I let the pH float upwards, it usually -- but not always -- stopped before 8.0. I also found that if I operated the pools between 7.6 and 8.0 it took FAR less acid, than if I tried to operate the same pool between 7. 2 and 7.6. (Note to Chem Geek: yes, I tried it both ways on the SAME pools )
    What you observed is completely consistent with the underlying chemistry. See this chart which shows how far out-of-equilibrium pool water is in terms of the excess carbon dioxide there is in the water. Pools are intentionally over-carbonated in order to provide a pH buffer and to add carbonates to protect plaster surfaces (when calcium is also added). You can see that at lower TA and higher pH the water is not as far out-of-equilibrium. The rate of carbon dioxide outgassing is related to this number, though Wojtowicz has shown that it is proportional to the square of the TA whereas my table doesn't include that effect (the table shows more of a linear effect with TA).

    So basically a pool will tend to rise in pH, but will do so more quickly at low pH and will slow down as the pH rises. It doesn't technically stop until it reaches equilibrium, but in practice it becomes so slow relative to other pH changes that it seems to be stable. This is because the carbonate alkalinity portion of TA is a SOURCE or rising pH itself due to carbon dioxide outgassing. It is not true that a higher TA will produce a more stable pH unless one has some acid added to the pool such as using Trichlor (or even Dichlor which is net acidic when accounting for chlorine usage/consumption since that is an acidic process). Instead, a higher TA will result in a faster pH rise and a higher ultimate equilibrium pH.

    The reason that it takes far less acid having the pH settle higher is that a higher pH results in less carbon dioxide in the water, all else equal. If you force a lower pH, you are forcing more of the carbonates in the water to be in the form of carbon dioxide and that will then outgas faster causing the pH to rise.

    You have chosen to use a higher target pH as a way of reducing the (further) pH rise, but the other approach is to lower the TA level itself. This will also result in a lower rate of pH rise. Assuming a CYA level of 30 (since some of this measures as TA), a pH of 7.8 with a TA of 80 ppm would have about the same amount of carbon dioxide as a pool with a pH of 7.5 and a TA of 45 ppm.

    On another related note: buffering has to do with how difficult it is to change the pH of a solution (your pool water in this case). Highly buffered water has highly stable pH . . . . IF the buffer in question is effective at that pH level.

    Most buffers have ranges over which they are effective, and other ranges over which they are not so effective. Cyanuric acid is an effective buffer at LOW pool pH levels, below 7.4 as I recall. Borax is an effective buffer at HIGH pH levels, above 8.0, I think. Total alkalinity tests measure how much buffer you have, but not which levels it's effective at.

    This is important, because if you have drifting pH levels like you do, it's your pool's buffer system that determines how hard you'll have to work to maintain your pH level. Absent aeration, sodium bicarbonate is an effective buffer in the 7.0 - 8.0 range where your pool lives. A pool with an effective bicarbonate based "Total Alkalinity" will require larger doses of acid, added less frequently, compared to a pool without that bicarbonate based buffer.

    More or less, a well buffered pool will require that you adjust your pH less frequently than a poorly buffered pool. It won't really decrease how much acid you need, but it will change how often you have to add it!
    It is not true that highly buffered water has a stable pH, even if the pH is in a good buffering range. The carbonates have TWO competing effects. The pH buffering effect where more is better AND the carbon dioxide outgassing effect where a higher TA is less stable pH (unless their are acid sources such as Trichlor). The latter effect dominates when the TA gets too high. As far as how high is "too high", this depends on the amount of water-air interchange so depends on aeration (i.e. waterfalls, spillovers, fountains, heavy splashing) so generally pools that are covered are more stable in pH even at higher TA levels.

    As for effective ranges of buffers, you don't have that quite right. In this post, I give more details about the buffering capabilities of the carbonates, cyanuric acid, and the borates. The borates have more pH buffering capacity against a rise in pH, but they do buffer both ways. The borate buffering system gets stronger as the pH rises. The carbonates, on the other hand, are the opposite where they get stronger in buffering as the pH gets lower (by higher and lower I'm referring to the normal 7.0 to 8.0 pool pH range). The cyanuric acid buffer system is a bit uneven in its buffering in this range.

    Total Alkalinity measures the buffer capacity in one direction only -- buffering against a drop in pH. This is why 50 ppm Borates only contributes 5 ppm to TA at a pH of 7.5. The borates have less buffer capacity against a drop in pH and have most of that capacity against a rise in pH. The measure for this would be Total Acidity, but that's not something in standard pool test kits and really isn't necessary to measure anyway since you can measure borates levels directly (the only real reason for the TA test is to indirectly measure the carbonates after adjusting for CYA and borates).

    Your statement about a pool with an effective bicarbonate TA needing large doses of acid less frequently is not true if the source of rising pH is due to the TA itself. If we ignore the outgassing of carbon dioxide from higher TA levels, then it is true that greater pH buffering results in a slower change in pH from other sources (say, curing plaster or Trichlor) but requires more acid or base to move the pH back to where it started.

    As for the amount of acid or base you need, it is true that the amount of buffering doesn't change that IF the buffer system itself isn't the source of pH change. So IF the rise in pH is due to carbon dioxide outgassing, then lowering the TA will result in less acid being needed over time and in a slower rise in pH. This is most especially true if the loss of pH buffering from the lower TA is made up for by using another pH buffer such as 50 ppm Borates.

    Richard
    Last edited by chem geek; 07-08-2010 at 10:03 PM.

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    Default Re: Algae, TA or what?

    Hi All;

    Richard, I've finally taken the time to look at your Pool Calculations spreadsheet. Very impressive! I started something similar, years ago, but got nowhere near as far as you have. I'm asking Madison (my older son, who's close to finishing his degree in biology) to start working through your spread sheet today.

    [ A couple of questions:
    1. Have you done the calculations for peroxide / chlorine interactions (dechlorination) and the interaction between monopersulfate and chlorine?
    2. It may be there, but do you have the calculation for the carbonate fraction of the TA, given a specific value for TA, CYA, & borates? Do you have an 'adjusted' SI, based on the presumptive carbonate ppm?
    3. Do you have a version with references to equation sources, etc.? ]

    Carl, Richard's calculations and analysis of the relations between pH change, TA, off gassing and so on are plausible. I can't verify them yet, but they do fit my own field experience, so that's confirmatory.

    My inclination, at this point, is to accept them -- and their implication that low TA is to be desired, generally -- for NON-concrete pools.

    I want to understand them better, and consider what the implications are on CONCRETE pools (and what Richard has to say) before jumping on them for concrete pools. There is some risk there, that a wrong judgment would lead to pool damage. However, that whole area of "what's happening to the plaster" is a realm of much more heat than light. Just about all the research done in that area has been paid for or done by folks with a really big axe to grind.

    I do think we need to be observant, and see if field reports from PF users confirm or dis-confirm the idea that lower TA (and particularly, lower carbonate alkalinity) leads to greater pH stability.

    I'm going to email you all (mods + Richard) a 'modest proposal'. I'll try to get it out today, but it may be tomorrow. Richard has done a LOT of work with gathering together the chemistry relevant to pools. Years ago, I found myself puzzled by the fact that, although most of the chemistry Richard is working with is not new (open to correction here) no one seemed to have put it "all together". Richard appears to have gone a very long way toward that.

    But, it's going to be hard (at least for me) to digest all that he's done, in order to get clear in my mind what to tell people.

    I do have one question to you all (that is, anyone who bothers to read this section, but particularly the mods and Richard):

    How interested are you all in changing pool chemistry -- not just for the 100,000 or so who follow PF and TFP closely -- but for the majority of pool users?

    I think I see a path to doing so, but it would require more than just Richard, and more than just me, working toward that end. It would be a worthwhile thing to do, I think.

    But it would (in the end) seriously affect BioLab as it exists today. And they drive the NSPF, many commercial pool codes, and the shape of "ideal" pool chemistry.

    (As you respond, keep in mind that BioLab probably will read this. When I last checked, several years ago, connections from their corporate network were ALL OVER this site and PoolSolutions.)

    Ben Powell

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    Default Re: Algae, TA or what?

    Quote Originally Posted by PoolDoc View Post

    Carl, Richard's calculations and analysis of the relations between pH change, TA, off gassing and so on are plausible. I can't verify them yet, but they do fit my own field experience, so that's confirmatory.

    My inclination, at this point, is to accept them -- and their implication that low TA is to be desired, generally -- for NON-concrete pools.

    ...

    I do think we need to be observant, and see if field reports from PF users confirm or dis-confirm the idea that lower TA (and particularly, lower carbonate alkalinity) leads to greater pH stability.

    ...

    But, it's going to be hard (at least for me) to digest all that he's done, in order to get clear in my mind what to tell people.

    I do have one question to you all (that is, anyone who bothers to read this section, but particularly the mods and Richard):

    How interested are you all in changing pool chemistry -- not just for the 100,000 or so who follow PF and TFP closely -- but for the majority of pool users?

    ...

    But it would (in the end) seriously affect BioLab as it exists today. And they drive the NSPF, many commercial pool codes, and the shape of "ideal" pool chemistry.

    (As you respond, keep in mind that BioLab probably will read this. When I last checked, several years ago, connections from their corporate network were ALL OVER this site and PoolSolutions.)

    Ben Powell
    I'm a big believer in doing what actually works, not what I'd like to think works, what everyone says works, or even the mantras I've followed for 9 or 10 years now.

    First off, let's divide "the world" into vinyl versus concrete/plaster pools as you suggest and keep this discussion solely to the vinyl (and I presume fiberglass) side. As you point out, the concrete/plaster side has all kinds of issues that may well require different standards than the vinyl side.

    So, only for vinyl pool owners I'd like to see us start collecting empirical evidence that Richard's and Evan's low TA theory ("theory" in the scientific sense, not the popular sense) is valid. It will probably take a few seasons but, frankly, even if it were shown to not be valid, I don't see it doing much harm to people's pools or swimming experiences. In other words, it's a safe test for us to run.

    In fact, I'll start lowering TA on my pool either tonight or this weekend--it's about 80, so getting it down to 50 should be a snap. Plus I've got my "splashers" to aerate it!

    As for the pool chem companies, we are already NOT where they want to be. Even with our current recommendations of TA of 80-125, we tell people that baking soda is chemically the same stuff as "Total Alkalinity Raiser" and that washing soda is chemically the same stuff as "pH Up!" (which also raises T/A). We further tell people to use muriatic acid to lower TA (by lowering pH).

    So we already advocate a T/A control system that does not require special chemicals only available from pool companies. If we simply move to advocating low T/A levels it doesn't affect them in any way that I can see.

    Our recommendations with regards to when to use chemicals only they can make readily and publicly available: CYA, Calcium, Polyquat 60%, Tri-Chlor, Di-chlor, Cal-Hypo and Sequestering agents, remains unchanged.

    So does our recommendations for chemicals to be avoided.

    Again, my own limited experience is that I've ONLY ever had a drastic change in pH, or even a constant change in pH where there was a clear, explanable cause, such as the time I came home after 2 weeks and found my CYA at 60 and my pH below 6.8. I had put 4 floaters full of Tri-Chlor tabs in my pool. The good news was I had no algae.....At the time I was not yet aware that Tri-Chlor was heavily acid--that must have been 2003.

    So, I guess what I would like to see is a set of TA levels recommended, somewhat similar to the table Richard has attached above, but, obviously with clearer guidelines (Not going for TA=40 and pH=8.0 to get perfect balance! )

    Carl
    Carl

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    Default Re: Algae, TA or what?

    Quote Originally Posted by PoolDoc View Post
    [ A couple of questions:
    1. Have you done the calculations for peroxide / chlorine interactions (dechlorination) and the interaction between monopersulfate and chlorine?
    2. It may be there, but do you have the calculation for the carbonate fraction of the TA, given a specific value for TA, CYA, & borates? Do you have an 'adjusted' SI, based on the presumptive carbonate ppm?
    3. Do you have a version with references to equation sources, etc.? ]
    :
    I want to understand them better, and consider what the implications are on CONCRETE pools (and what Richard has to say) before jumping on them for concrete pools.
    :
    Years ago, I found myself puzzled by the fact that, although most of the chemistry Richard is working with is not new (open to correction here) no one seemed to have put it "all together". Richard appears to have gone a very long way toward that.
    1. I don't have hydrogen peroxide in the spreadsheet, but I've done the calculations for using it as a dechlorinator since people have asked about that. Roughly speaking, it takes the same volume of 3% hydrogen peroxide to neutralize a volume of 6% bleach (detailed calculations are in this post). As for monopersulfate, I do have the equivalent of that in the spreadsheet at line 359 "[HSO5-] assumed to be equal to [HSO4-]" which is a field that gets calculated when you enter in a quantity into the "NON-CHLORINE SHOCK" section. You can then adjust FC so that line 293 "Free Chlorine" matches in amount to 359 and that will give you the chlorine equivalent for the MPS. A pain, yes, but this question doesn't come up very much. Roughly speaking 3-1/2 teaspoons of Dichlor is equivalent to 5 fluid ounces of 6% bleach is equivalent to 7 teaspoons of non-chlorine shock (43% MPS) and is 7 ppm FC in 350 gallons and is the amount of oxidizer needed for every person-hour of soaking in a hot (104ºF) tub.

    2. Yes, the Carbonate Alkalinity is in the first section on line 16. The S.I. calculations all use this adjusted TA (i.e. the carbonate alkalinity). I do not have any raw unadjusted S.I. using TA alone (that is, ignoring CYA and Borates). Note that my S.I. calculation comes from direct calculation of calcium and carbonate ion concentrations relative to the solubility product of calcium carbonate. I also derive the LSI formula in lines 436 through 481 which shows that it comes directly from the equilibrium of calcium and carbonate ions with calcium carbonate and has nothing to do with boiler systems, open vs. closed, etc.

    3. I don't have a references chart, but I list a few in the spreadsheet. The constants for the chlorinated isocyanurates and for CYA come from the 1974 O'Brien paper. The most flaky, yet critically important, constant in the spreadsheet is for the solubility product of calcium carbonate where I ended up using consistent data from the CRC Handbook that resulted in closely matching the Taylor watergram. I also have constants from Wojtowicz that are used when you set 223, 224 and 225 (last three lines in that block) to TRUE in columns B and C. The ANSI/APSP-11 settled on S.I. tables that are a little closer to Wojtowicz are are generally 0.1 higher than my calculation (Wojtowicz is generally 0.15 higher than my calculation). The ion pair dissociation constants come from formation or stability constants mostly in a spreadsheet source I saved but would have to look up where that came from -- they aren't critical and only affect the saturation index by about 0.02 (unless sulfates are very high).

    Using a lower TA in a concrete ("pool plaster") pool is fine so long as you compensate other parameters such as pH and/or Calcium Hardness (CH) to get the saturation index to near zero. This will saturate the water with calcium carbonate to protect such surfaces. Basically, the lower TA lowers carbonate ion but a higher pH does the opposite while CH increases calcium. Theoretically, a low TA and high CH combination is better in terms of calcium oxide since calcium carbonate saturation implies a constant right-hand side product while lower TA means a lower carbon dioxide amount on the left-hand side:

    CaO + CO2 <---> Ca(2+) + CO3(2-) + heat

    The calcium oxide is bound tightly in pool plaster mostly as 3CaO•2SiO2•4H2O while the above reaction is very much thermodynamically favored to the right (the reverse reaction starting from calcium carbonate is how cement is made in a kiln along with silicates).

    The chemistry I've been working on is not new. I've just been putting together existing pieces The latest breakpoint chlorination model (chlorine oxidation of ammonia) is from 1992 and 2000. I also follow current disinfection by-product research, mostly by Ernest "Chip" Blatchley, from 2007, 2009 to present-day.

    Richard
    Last edited by chem geek; 07-09-2010 at 11:39 AM.

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    Default Re: Algae, TA or what?

    Quote Originally Posted by CarlD View Post
    In fact, I'll start lowering TA on my pool either tonight or this weekend--it's about 80, so getting it down to 50 should be a snap. Plus I've got my "splashers" to aerate it!
    Carl,

    Unless your pool experiences a regular rise in pH over time, then lowering the TA isn't going to show any noticeable difference. Also, there is a slow upward pressure on pH from chlorinating liquid and bleach due to the "excess lye" and this varies by brand with 6% Clorox Regular unscented having the lowest with a pH of 11.9. Some off-brand bleaches have a pH of 12.5 or higher. Chlorinating liquid also varies with better 12.5% brands having a pH of 12.5 while others have 13 or higher. If you tell me the concentration and pH of your chlorine product and how much FC you use per day on average, I can tell you the pH rise (with TA assumptions) and amount of acid you need to compensate. No matter how low you lower the TA, you won't get rid of the need to compensate for this "excess lye".

    As for recommended TA levels, when using a hypochlorite source of chlorine you generally don't want to go above 80 ppm, but with covered pools a higher TA isn't going to be much of a problem. As for how low to go, that depends on how much aeration there is in the pool and isn't easily calculated. So one would just have a more generic rule for those pools experiencing a regular rise in pH of letting the TA drop as low as 50 ppm if needed and seeing if this improves the rate of pH rise and then compensate pH and/or CH. For most pools, 70-80 ppm will be OK. It's SWG pools and pools with water aeration features that have more of an issue, partly due to increased aeration from hydrogen gas bubbles (though calculations show this probably isn't the entire effect) but also, I believe, from undissolved chlorine gas outgassing. This latter effect can't be compensated by TA and is probably worse in pools with short pipe runs from the SWG to the pool.

    As for the point one needs to get in the carbon dioxide equilibrium chart before pH becomes stable, that is only able to be determined empirically and will be different for every pool since the rate of outgassing depends on the amount of air-water surface interaction so on aeration, wind, etc. Very roughly speaking, nearly everyone (with no pool cover) experiences a problem when they get into the red region with 20 or more times as much carbon dioxide in the water than the equilibrium amount from air, many have a problem in the orange region between 10 and 20, and most seem to do OK with some pH rise that is tolerable in the green region less than 10, but there are definitely those highly aerated pools who see a rise in pH until they get down to nearly 2 in the chart. For spas, the hotter temperature and vastly increased aeration from spa jets almost always has to get below 4 and sometimes down to 2 or 1 before the pH becomes stable. The use of 50 ppm Borates provides additional pH buffering when the TA is low, but without the negative pH rising side effect of the carbonate buffer system.

    Thanks,
    Richard
    Last edited by chem geek; 07-09-2010 at 12:01 PM.

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