Oxygenation experiments with hydrogen peroxide

Australia & New Zealand Homebrewing Forum

Help Support Australia & New Zealand Homebrewing Forum:

This site may earn a commission from merchant affiliate links, including eBay, Amazon, and others.
Numbers from yesterday:
Gravity-25thMay1.png
Att-25thMay1.png

#1 is basically 24hrs behind the Control.

MHB said:
So if the results mean anything, there would be no good time to add peroxide to a brew.
Hopefully you will get an Oxy kit and repeat the experiment with oxygenated wort, against an unaerated control.

Like I said before, its good to see someone documenting the results of an experiment, and put them up so others can see what happens
Appreciated Mark
I think one of the interesting comparisons is #2 vs #1, where #1 shows a distinctly better attenuation profile - why is this? The difference was likely down to the absence or presence of yeast catalase which has been shown to act as a catalyst in the 2H2O2 -> 2H2O + O2 reaction.

The actual dosage into #1 was 320ppm H2O2, or 0.032% in the 150mL starter. I said 160ppm but this was really the maximum potential O2, and it didn't necessarily get there. I gave it 40min in an unmixed situation to break down everything into O2, but a few web references (e.g. this one here, where the lowest was 0.09% or about 3x stronger) point to low concentrations like this taking potentially a number of hours to fully break down. I'm not picking up any yeast health issues at this stage from getting whacked with 320ppm H2O2 either, even though yeast is apparently only equipped to deal with ppb levels....... we will see in future tasting though. I will get a few of the CQ guys to have a taste and will probably throw a few around the Brisbane swap to get some feedback.

I'm leaning towards another experiment comparing stirplate and stirplate + H2O2 in a split lager batch. I would hope that stirring and 4-6hrs would be enough time to decompose the H2O2 to O2, with any excess just leaving as O2 gas. This for me would be the real test as I want something simple to help push lagers along rather than having a wand, stone, O2 regulator and bottle getting used for 5min once a month and being unused in the shed for the rest of the time.

It would be good to see an experiment with gaseous O2 into the wort before pitching to compare wort freshness vs H2O2 on a stirplate, as well as the attenuation comparison. Although H2O2 does have a higher oxidation potential than gaseous O2, I wonder how much wort freshness is being lost with oxygenation prior to pitching?
 
Try to take this the way its intended, I have said I admire the dedication and work you have done.
Where it breaks down for me is in your interpretation of the results.
When I look at the results as reported my first observation is that in every case where peroxide was added the ferment was slower or even less complete. Clearly #3&4 aren't encouraging, so on the evidence adding H2O2 to the wort isn't a good idea.
Which leaves adding H2O2 to the Starter - comparing control and #1

Looking at the results of C and #1 and your reporting that #1 smells/tastes OK, the attenuation profile looks to me exactly like you would expect to get with a Higher (C) and lower (#1) pitch rate of very similar yeast.
The obvious conclusion being that adding H2O2 to the starter reduced the amount of or vitality of the yeast. Another day or two should tell the story, but I suspect that C and #1 will be fairly similar by the time the smaller yeast population in #1 is finished. Sorry to say this to indicates that there was no benefit from adding H2O2 to the starter - In fact in terms of fermentation processes there is really not much difference between a starter and a ferment - except that the intention in one is to increase the yeast population and vigor, in the other to use the yeast to make alcohol. The metabolic pathways and nutrient demands are the same.

If you want to persist in trying to make Peroxide breakdown into O2 try adding a bit of Silver to the starter (a pinkie ring, ear ring, silver chain, charm... anything that you can pinch from a jewellery box) Silver will break down the peroxide very quickly, silver and its salts are toxic to yeast so I would pull it out before adding the yeast. Just don't add too much peroxide to a closed container with silver, the reaction is very fast and quite exothermic (can get very hot), I was discussing this with a mate (better chemist than me) and we coined the term PeroxieBomb.
I haven gathered up some parts to make a small reactor to convert H2O2 to O2 and deliver it to the wort, its basically an Oxy kit without bottled oxygen, before anyone gets too excited, the upfront cost is less, the cost of peroxide/O2 gas is way higher (TANSTAAFL) but that's life.

When your at the club, ask around I'm sure someone would be willing to lend you an O2 kit, I strongly suspect that there are enough people here interested in the results that people would be more than happy to help. I also think that using O2 will really make a significant difference.

Good luck and I am looking forward to your further results.
Mark
 
Definitely fantastic to see a well documented comparison. Great job Adr_0
Starting to get interesting with the results!

I'd agree the early numbers seem to indicate the H2O2 idea is not a good one in reality.

However, we need to let it play out to completion and see the *final* results, namely the FG and the sensory perceptions of quality.
And then, ideally, do the same again but with the Control & #1, plus O2 into a starter, and O2 into the FV. It'd complete the full comparison nicely, and confirm the benefits (or lack thereof) of both approaches.

Thanks again to Adr_0 !!


EDIT: as an aside, i'm curious as to why the fermentation curves are all "wobbly" like a flat sine curve, etc? Simply from minor temp fluctuations, perhaps?
 
MHB said:
Try to take this the way its intended, I have said I admire the dedication and work you have done.
Where it breaks down for me is in your interpretation of the results.
When I look at the results as reported my first observation is that in every case where peroxide was added the ferment was slower or even less complete. Clearly #3&4 aren't encouraging, so on the evidence adding H2O2 to the wort isn't a good idea.
Which leaves adding H2O2 to the Starter - comparing control and #1

Looking at the results of C and #1 and your reporting that #1 smells/tastes OK, the attenuation profile looks to me exactly like you would expect to get with a Higher (C) and lower (#1) pitch rate of very similar yeast.
The obvious conclusion being that adding H2O2 to the starter reduced the amount of or vitality of the yeast. Another day or two should tell the story, but I suspect that C and #1 will be fairly similar by the time the smaller yeast population in #1 is finished. Sorry to say this to indicates that there was no benefit from adding H2O2 to the starter - In fact in terms of fermentation processes there is really not much difference between a starter and a ferment - except that the intention in one is to increase the yeast population and vigor, in the other to use the yeast to make alcohol. The metabolic pathways and nutrient demands are the same.

If you want to persist in trying to make Peroxide breakdown into O2 try adding a bit of Silver to the starter (a pinkie ring, ear ring, silver chain, charm... anything that you can pinch from a jewellery box) Silver will break down the peroxide very quickly, silver and its salts are toxic to yeast so I would pull it out before adding the yeast. Just don't add too much peroxide to a closed container with silver, the reaction is very fast and quite exothermic (can get very hot), I was discussing this with a mate (better chemist than me) and we coined the term PeroxieBomb.
I haven gathered up some parts to make a small reactor to convert H2O2 to O2 and deliver it to the wort, its basically an Oxy kit without bottled oxygen, before anyone gets too excited, the upfront cost is less, the cost of peroxide/O2 gas is way higher (TANSTAAFL) but that's life.

When your at the club, ask around I'm sure someone would be willing to lend you an O2 kit, I strongly suspect that there are enough people here interested in the results that people would be more than happy to help. I also think that using O2 will really make a significant difference.

Good luck and I am looking forward to your further results.
Mark
Looking at the results, yes my method of a quick spin on the stir plate is the best performer. And I agree that the #1 sample had yeast of either less quantity or less vitality.

I guess the million dollar question is:
-was cell count reduced by adding 320ppm worth of H2O2; or
-was not enough O2 produced, meaning the yeast did not have enough vitality?

If the first one is true, perhaps less -
or no - peroxide should have been added. If the second is true, I should have waited longer before pitching.

I'm not sure that you or I can answer this, and though I've had a quick look through some papers I certainly can't say confidently one way or the other, though I am leaning towards not enough time to produce the O2 - based on how slow O2 production is at low total concentrations.

What do you you think about #2, where the peroxide was in suspension for 40min before yeast? Do you think the peroxide reduced the yeast count, or was mostly used up oxidising the wort leaving very little to produce O2 once the yeast was added?


technobabble66 said:
Definitely fantastic to see a well documented comparison. Great job Adr_0
Starting to get interesting with the results!

I'd agree the early numbers seem to indicate the H2O2 idea is not a good one in reality.

However, we need to let it play out to completion and see the *final* results, namely the FG and the sensory perceptions of quality.
And then, ideally, do the same again but with the Control & #1, plus O2 into a starter, and O2 into the FV. It'd complete the full comparison nicely, and confirm the benefits (or lack thereof) of both approaches.

Thanks again to Adr_0 !!


EDIT: as an aside, i'm curious as to why the fermentation curves are all "wobbly" like a flat sine curve, etc? Simply from minor temp fluctuations, perhaps?
The wobbles would be temperature fluctuations due to the low volumes (2.5L) vs the main 12L batch.
 
Adr_0 said:
Snip
What do you you think about #2, where the peroxide was in suspension for 40min before yeast? Do you think the peroxide reduced the yeast count, or was mostly used up oxidising the wort leaving very little to produce O2 once the yeast was added?
I suspect its moot - either way no gain in fact a loss of ferment vigor, I mean I suspect you could spend a lot of time working out when adding H2O2 does the least harm, but what's the point?
Mark
 
Hi Adr

Sorry if I missed it, but what grade of hydrogen peroxide did you use? Do you know what stabilising agents were in it?
 
If it was Goldcross H2O2 then the main stabiliser is phosphoric acid with traces of phenacetin and it is pharmaceutical grade.
 
MHB said:
...
When I look at the results as reported my first observation is that in every case where peroxide was added the ferment was slower or even less complete. Clearly #3&4 aren't encouraging, so on the evidence adding H2O2 to the wort isn't a good idea.
Which leaves adding H2O2 to the Starter - comparing control and #1
...
Sorry to say this to indicates that there was no benefit from adding H2O2 to the starter
This was the conclusion I came to in my comparison brew also (although not as thorough an experiment as Adro's)

Adr_0 said:
Looking at the results, yes my method of a quick spin on the stir plate is the best performer. And I agree that the #1 sample had yeast of either less quantity or less vitality.
I guess the million dollar question is:
-was cell count reduced by adding 320ppm worth of H2O2; or
-was not enough O2 produced, meaning the yeast did not have enough vitality?

If the first one is true, perhaps less -
or no - peroxide should have been added. If the second is true, I should have waited longer before pitching.

I'm not sure that you or I can answer this, and though I've had a quick look through some papers I certainly can't say confidently one way or the other, though I am leaning towards not enough time to produce the O2 - based on how slow O2 production is at low total concentrations.

What do you you think about #2, where the peroxide was in suspension for 40min before yeast? Do you think the peroxide reduced the yeast count, or was mostly used up oxidising the wort leaving very little to produce O2 once the yeast was added?
I would think vitality is the key. I know with my H2O2 experiment there were obvious signs of yeast stress in; greater ester production, less flocculation and a greater amount of time to reach same attenuation. Hence why I came to the conclusion that there was no benefit of H2O2 for the fermentation side of things. My reasoning being that if H2O2 can't beat simple aeration then it is of little use to fermentation full stop. My results of the pure side by side comparison are very similar to your Control V #1. As MHB points out #2 & #3 are clear signs of yeast under strain. Now this maybe due to differing size of your test fermentations or amount of yeast per test, but the consistent sign is that the vitality of the yeast is degraded by the H2O2 addition. Whether the reason is that it is because of H2O2 effecting the yeast or because H2O2 has no effect, but produces too little O2 to improve vitality is mute as MHB points out. The fact that no obvious positive advantage is given is enough indication that H2O2 is of little value in a practical sense.

MHB said:
I suspect its moot - either way no gain in fact a loss of ferment vigor, I mean I suspect you could spend a lot of time working out when adding H2O2 does the least harm, but what's the point?
Mark

Adr_0 said:
I'm leaning towards another experiment comparing stirplate and stirplate + H2O2 in a split lager batch. I would hope that stirring and 4-6hrs would be enough time to decompose the H2O2 to O2, with any excess just leaving as O2 gas. This for me would be the real test as I want something simple to help push lagers along rather than having a wand, stone, O2 regulator and bottle getting used for 5min once a month and being unused in the shed for the rest of the time.

It would be good to see an experiment with gaseous O2 into the wort before pitching to compare wort freshness vs H2O2 on a stirplate, as well as the attenuation comparison. Although H2O2 does have a higher oxidation potential than gaseous O2, I wonder how much wort freshness is being lost with oxygenation prior to pitching?
I think the stirplate v stirplate + H2O2 experiment is a fairer comparison and I would expect will result in a similar outcome to my aerated v pure H2O2 experiment (but am keenly awaiting you to prove my expectation wrong). Your comment about the wand, stone, O2 bottle etc was exactly why I gave H2O2 a go. I will be borrowing a bottle of O2 and regulator to hook up to my recent purchase of a wand and stone and be giving it a test on my next lager batch to see if there is great improvement (I anticipate due to the experience of others that it will be). I would be very interested in a comparison of the stirplate vitality starter method V Oxygenation, but that will have to wait until I can get my hands on a stirplate.

To look at your question of O2 effect on 'freshness' of the wort - I'll quote someone with experience in the area of the question and whilst I know you know (and most currently participating in this thread) (I did before I began my experiment, which is why a main part of my experiment is the long term sensory testing), but just a reminder of what DrSmurto posted back in Feb on the O2 thread for those looking at this in the future;
DrSmurto, on 17 Feb 2017 - 11:04 AM, said:
I've only very briefly skimmed the discussion on H2O2.
A few points from a scientist whose research area involves H2O2 and O2 in juice/wine; similar situation holds with wort/beer.
Firstly, the reason why O2 is used and not H2O2 is that O2 can't react with organic compounds. This is what is called 'spin forbidden' and is a very fundamental principle of chemistry relating to the configuration of the electrons in the atom. It first reacts with transition metal ions to produce the superoxide radical which can then react with organic compounds. Yeast can mop up the oxygen very rapidly and in a medium that contains only trace amounts of reactive transition metals in the required oxidation state, it will do so before much, if any damage is caused by oxygen via the superoxide radical. We have measured the speed in which yeast uses up all the oxygen in juice and it is very fast, in the order of minutes. We can also measure oxidation markers to see what chemical effects are being caused by O2 introduction and the result is negligible. Our oxygen sensors measure down to ppb levels of oxygen.
This is not the case with hydrogen peroxide, it is very capable of reacting with organic compounds or just about anything it comes into contact with. This is not a selective process, you can't expect yeast to protect the wort from H2O2 as it cannot prevent every single molecule of H2O2 from colliding with other molecules in the wort. Adding an incredibly powerful oxidiser to your wort is not a particularly well thought out method of adding O2.
DrSmurto, on 17 Feb 2017 - 1:55 PM, said:
Sulfite/sulfur dioxide is added to wine for 2 reasons. To protect the wine from microbial spoilage, which in combination with the low pH of wine provides protection (sulfite exists in 3 forms depending on the pH - sulfur dioxide, bisulfite, sulfite). The other reason is it is an anti-oxidant. It is there to protect the wine from oxygen. The vast majority of wine is bottled with no yeast present at all so a defence against O2 is needed. As I mentioned previously, O2 get's converted to the superoxide radical via transition metals. This is converted to hydrogen peroxide. At this point, sulfite reacts with it to remove it from the wine. If there is no sulfite present, the superoxide is further reduced by another transition metal to an even more reactive molecule, the hydroxide radical. This, for example, reacts with ethanol to produce acetaldehyde. The last step in this reaction is known as the 'Fenton Reaction'.
So if you are adding hydrogen peroxide to wort you have skipped one reduction step, also known as the rate limiting step, and provided the system with a highly reactive molecule that otherwise would not exist in any substantial quantity if you had added oxygen. We don't measure H2O2 directly, we use the reduction in sulfite to measure the amount of hydrogen peroxide produced and the kinetics of the reaction. There is plenty of research in this area and it is ongoing.
I can't stress this enough. H2O2 is a very powerful oxidant, it will react with any molecule it comes in to contact with. I use it to 'digest' wine (it breaks apart the complex molecules and within hours, red wine looks like the palest white wine), clean glassware. In combination with concentrated sulfuric acid, it's used to etch glass. It is used to power rockets. It's one of those chemicals you treat with the utmost respect, particularly if you are using 30% or greater concentrations.
EDIT - Sorry the quote didn't transfer across as a quote, so I have quoted it!
 
Jack of all biers said:
This was the conclusion I came to in my comparison brew also (although not as thorough an experiment as Adro's)

I would think vitality is the key. I know with my H2O2 experiment there were obvious signs of yeast stress in; greater ester production, less flocculation and a greater amount of time to reach same attenuation. Hence why I came to the conclusion that there was no benefit of H2O2 for the fermentation side of things. My reasoning being that if H2O2 can't beat simple aeration then it is of little use to fermentation full stop. My results of the pure side by side comparison are very similar to your Control V #1. As MHB points out #2 & #3 are clear signs of yeast under strain. Now this maybe due to differing size of your test fermentations or amount of yeast per test, but the consistent sign is that the vitality of the yeast is degraded by the H2O2 addition. Whether the reason is that it is because of H2O2 effecting the yeast or because H2O2 has no effect, but produces too little O2 to improve vitality is mute as MHB points out. The fact that no obvious positive advantage is given is enough indication that H2O2 is of little value in a practical sense.



I think the stirplate v stirplate + H2O2 experiment is a fairer comparison and I would expect will result in a similar outcome to my aerated v pure H2O2 experiment (but am keenly awaiting you to prove my expectation wrong). Your comment about the wand, stone, O2 bottle etc was exactly why I gave H2O2 a go. I will be borrowing a bottle of O2 and regulator to hook up to my recent purchase of a wand and stone and be giving it a test on my next lager batch to see if there is great improvement (I anticipate due to the experience of others that it will be). I would be very interested in a comparison of the stirplate vitality starter method V Oxygenation, but that will have to wait until I can get my hands on a stirplate.

To look at your question of O2 effect on 'freshness' of the wort - I'll quote someone with experience in the area of the question and whilst I know you (and most currently participating in this thread) (I did before I began my experiment, which is why a main part of my experiment is the long term sensory testing), but just a reminder of what DrSmurto posted back in Feb on the O2 thread for those looking at this in the future;

EDIT - Sorry the quote didn't transfer across as a quote, so I have quoted it!
Firstly, I used 12% from Anpros diluted up to 10x weight which should be 1.2%. In 150mL starter this ended up as 320ppm or ~9-10mM. In 2.5L of wort this was 19ppm or 0.5mM.

Based on concentrations I would expect viability of #2 to be significantly higher than #1.

I can understand the cause of the poor performance in #2 being a moot point because it's rooted anyway, but understanding the reason for and how it can be compared to #1 (e.g. comparison of viability/viable cells, cell vitality) is of interest to me. Technically #1 should have copped the biggest hit to viability, given the high concentration - and the hit to viability should have been massive if it were in its exponential growth stage. Conversely #2 should have been insulated to a degree from the H2O2, assuming that it was too busy oxidising wort to challenge the yeast.

Given as well that #1 had no additional oxygenation while the control spent 6hrs on a stirplate, I'm leaning towards O2 having been produced at some point in #1 - otherwise it would have performed a lot worse.

So I'm keen to do a stirplate test, likely with lower concentration and at the end of the growth phase (in the starter). The pre-exposure to oxygen and being in the stationary phase should significantly reduce the lost viability, and the additional time on the stirplate (6hrs vs 40min in my first test) should give it the chance to produce oxygen.


Just a grab from above:
"A few points from a scientist whose research area involves H2O2 and O2 in juice/wine; similar situation holds with wort/beer.
Firstly, the reason why O2 is used and not H2O2 is that O2 can't react with organic compounds. This is what is called 'spin forbidden' and is a very fundamental principle of chemistry relating to the configuration of the electrons in the atom. It first reacts with transition metal ions to produce the superoxide radical which can then react with organic compounds. Yeast can mop up the oxygen very rapidly and in a medium that contains only trace amounts of reactive transition metals in the required oxidation state, it will do so before much, if any damage is caused by oxygen via the superoxide radical. We have measured the speed in which yeast uses up all the oxygen in juice and it is very fast, in the order of minutes. We can also measure oxidation markers to see what chemical effects are being caused by O2 introduction and the result is negligible. Our oxygen sensors measure down to ppb levels of oxygen."

I'm curious about this, as I thought this was the basis for all oxidation of wort compounds and aeration water treatment. I would expect the reaction rates with gaseous O2 would be slower if the reactions are spin forbidden, but they will still happen. I can appreciate that gaseous O2 is preferred as it is less reactive, but it's still reactive. I guess the phase of adding the O2 - prior to significant growth and fermentation - helps this significantly, but I'm curious about staling before yeast is added. I guess to my mind, yeast should be pitched then the wort oxygenated but I'm not sure that everyone does this.
 
Adr_0 said:
Firstly, I used 12% from Anpros diluted up to 10x weight which should be 1.2%. In 150mL starter this ended up as 320ppm or ~9-10mM. In 2.5L of wort this was 19ppm or 0.5mM.

Based on concentrations I would expect viability of #2 to be significantly higher than #1.
Please don't take my comments as a criticism. The problem with H2O2 is the randomness in which it will give up the O- and which molecules that O- react with. It could be that randomly the conditions of #2 meant that the O- reacted more with the wort and next time the experiment is repeated with the exact same circumstances instead of reacting with the wort molecules it reacts with other O- and creates O2. I guess this is the point DrSmurto was trying to point out.
Adr_0 said:
Given as well that #1 had no additional oxygenation while the control spent 6hrs on a stirplate, I'm leaning towards O2 having been produced at some point in #1 - otherwise it would have performed a lot worse.
Absolutely, and was my observations too, but given the stirplate performed better (similar to my experiment only just) then the O2 take up from simple stirplate is better than the best H2O2 sample produces O2 for the yeast. Never said it doesn't work at all, just that it doesn't seem to create better conditions than aeration (given the stirplate is really only continuous aeration).

Adr_0 said:
Just a grab from above:
"A few points from a scientist whose research area involves H2O2 and O2 in juice/wine; similar situation holds with wort/beer.
Firstly, the reason why O2 is used and not H2O2 is that O2 can't react with organic compounds. This is what is called 'spin forbidden' and is a very fundamental principle of chemistry relating to the configuration of the electrons in the atom. It first reacts with transition metal ions to produce the superoxide radical which can then react with organic compounds. Yeast can mop up the oxygen very rapidly and in a medium that contains only trace amounts of reactive transition metals in the required oxidation state, it will do so before much, if any damage is caused by oxygen via the superoxide radical. We have measured the speed in which yeast uses up all the oxygen in juice and it is very fast, in the order of minutes. We can also measure oxidation markers to see what chemical effects are being caused by O2 introduction and the result is negligible. Our oxygen sensors measure down to ppb levels of oxygen."

I'm curious about this, as I thought this was the basis for all oxidation of wort compounds and aeration water treatment. I would expect the reaction rates with gaseous O2 would be slower if the reactions are spin forbidden, but they will still happen. I can appreciate that gaseous O2 is preferred as it is less reactive, but it's still reactive. I guess the phase of adding the O2 - prior to significant growth and fermentation - helps this significantly, but I'm curious about staling before yeast is added. I guess to my mind, yeast should be pitched then the wort oxygenated but I'm not sure that everyone does this.
My understanding of DrSmurto's quote is that O2 can react with metal ions (iron & copper for example), but won't with the organic compounds in wort. I've emboldened the step above. It is this step that then allows O- to later split off the metal molecules and either form H2O2 which then can react with the organic compounds (wort/beer) or just react with the organic compounds straight up. Thus creating the oxidisation flavours we like to avoid. What he is saying is that with low amounts of these metal ions plus the speed in which yeast consume the more stable O2 makes the likelihood of this random splitting of O2 into a superoxide radical lower and therefore less O- radicals are later produced. This is all very complicated chemistry, which is above my head, so if what I understand from DrSmurto's comments is wrong please feel free to correct me, but I have read similar elsewhere.

EDIT - this article mentions the above O2 to metal oxidation reactions, but only briefly, but it's all I can find that is relevant to brewing.
View attachment 03 - The role of oxygen.pdf
 
Jack of all biers said:
Please don't take my comments as a criticism. The problem with H2O2 is the randomness in which it will give up the O- and which molecules that O- react with. It could be that randomly the conditions of #2 meant that the O- reacted more with the wort and next time the experiment is repeated with the exact same circumstances instead of reacting with the wort molecules it reacts with other O- and creates O2. I guess this is the point DrSmurto was trying to point out.

Absolutely, and was my observations too, but given the stirplate performed better (similar to my experiment only just) then the O2 take up from simple stirplate is better than the best H2O2 sample produces O2 for the yeast. Never said it doesn't work at all, just that it doesn't seem to create better conditions than aeration (given the stirplate is really only continuous aeration).

I agree with and understand the above, which is why I tried to dilute the peroxide somewhat - to assist in mixing. I would imagine the activation energy of the reactions between peroxide and wort compounds is less than the activation energy to go to 2H2O + O2 [possibly with the exception of being catalysed by catalase or glutathione], so the randomness is more a matter of how good the mixing is. This is also why I think we're all in agreement that putting peroxide into wort without yeast isn't a good idea. And even with yeast, putting it into a large volume of wort is probably also asking for trouble - so the concentration of yeast (catalase and glutathione) vs wort should be as high as possible, hence the starter.

While the 'best H2O2 sample' may have been true in this experiment, it's not necessarily the best way to do it. There has been a tremendous amount I've learned - hopefully a few of us have learned a bit - and I would like to try something else which should be more definitive. I don't think it's reasonable to draw future conclusions from this very specific set of circumstances (those around the #1 sample).

Your H2O2 example seemed to be very well mixed and H2O2 progressively added and is probably a better executed version of my #3. Looks like 24-25ppm H2O2 and 0.7mM concentration, which was significantly below my #1 of 320ppm H2O2 and 9-10mM concentration. I wonder if there has been preferential wort oxidation in your version. Even in the presence of yeast that concentration is extremely low, so it's likely going to take a very long time to produce the O2

My understanding of DrSmurto's quote is that O2 can react with metal ions (iron & copper for example), but won't with the organic compounds in wort. I've emboldened the step above. It is this step that then allows O- to later split off the metal molecules and either form H2O2 which then can react with the organic compounds (wort/beer) or just react with the organic compounds straight up. Thus creating the oxidisation flavours we like to avoid. What he is saying is that with low amounts of these metal ions plus the speed in which yeast consume the more stable O2 makes the likelihood of this random splitting of O2 into a superoxide radical lower and therefore less O- radicals are later produced. This is all very complicated chemistry, which is above my head, so if what I understand from DrSmurto's comments is wrong please feel free to correct me, but I have read similar elsewhere.

I'm fine with that. Sorry, my comment on this was a little clumsy so I'll try again.

My main point was oxygenation of the wort prior to adding yeast, which seems to be pretty common, possibly will still oxidise the wort. It's not going to be the same as H2O2 into wort, but without yeast - like H2O2 without yeast - will the wort just get oxidised? If trace transition metals are there and there is no yeast to mop up O2, I would say yes - to what degree I'm unsure. We could say this is also a moot point, that oxygenation should only be done after adding yeast so it's not worth looking at, but I'd argue there are enough people doing it that it's worth a look.

EDIT - this article mentions the above O2 to metal oxidation reactions, but only briefly, but it's all I can find that is relevant to brewing.
attachicon.gif
03 - The role of oxygen.pdf
Added comments to quote

I'm fine with the high oxidation potential of H2O2 in wort, which is why I'm continuously leaning towards lower concentration and dilution in a yeast-heavy environment rather than into wort. From what I've read as well this should be with the yeast in a stationary state. At low concentrations, with pre-exposure to oxygen and with the yeast in a stationary state the viability is maintained. A yeast-heavy environment such as a starter should be well equipped to handle the challenge of H2O2, and given enough time the yeast should readily take up O2.

We'll see anyway...
 
I'd agree with your line of reasoning, Adr_0, and would similarly wonder about the possible staling reactions from O2, compared to those of H2O2. However, one thought has occurred to me: the temperature could be a critical factor in the difference. HSA and the reactions involved are (now?) theorized to have a "sweet" spot somewhere ~60-70*C (from memory). Meaning above that O2 doesn't dissolve into the wort much, and below that the reaction rate is too slow. So basically the temp we're talking about when pitching yeast is too low for staling reactions from O2. Whereas H2O2 disassociates fairly well at pitching temps. It would still technically fall under the point you made earlier that O2-derived staling reactions may occur very slowly, but they'd still occur. However, it may help understand why the amount of staling reactions could be so dramatically different. Just a suggestion!
I'll maybe try to get around to going over the details of what DrS & JoaB posted sometime tomorrow.
I'd definitely be looking at low dilution (ie: weak) additions to a high yeast solution. Also maybe consider multiple additions - eg: instead of 20ml in 1 hit, maybe 5ml first (yeast initiates catalase production) then a few more 5ml additions every 30-60mins thereafter. Just another suggestion! [emoji1]
 
Yes, you are probably right.

Next set of numbers:
Gravity-28thMay1.png
Att-28thMay1.png

So we've hit terminal gravity, which is nice. I think I'll give it a couple more days at 20°C, but this #2 is being a right royal PITA and starting to hold things up. I think I'll start to gently swish, perhaps daily, to get the gravity down so that I can bottle.
 
So, bottling today. Bottling will be done by pre-purging bottles with CO2 and also topping off the headspace with CO2 to minimise the impact of bottling oxidation on the end product.

Firstly, a summary of time vs fG:

Control - 7 days
1......+1day/24hrs
2......+10 days
3......+5 days

I took a shot of the three test batches as well for curiosity. From left to right (1, 3, 2) which I'm guessing suggests decreasing yeast growth - or at least decreasing total yeast cells:
sediment-1-3-2.jpg

So, in simplistic terms, the resulting samples from this experiment where H2O2 was added did not provide yeast vitality, viability or attenuation benefit vs a control batch aerated for 6hrs on a stirplate. It is unknown whether any benefit could have been provided vs an un-aerated batch.

In terms of dosing, the starter in #1 had around 320ppm/10mM H2O2 once in solution which is considered by most literature to be a fairly detrimental dose, however still significantly out-performed #2 and #3 where H2O2 concentration was closer to 20ppm/0.6mM, suggesting that oxygen was potentially produced in greater volume than in #2 and #3.

The significant difference in attenuation profiles and yeast volume between #2 and #3 suggest that H2O2 is - as per scientific consensus and literature - going to favour wort oxidation reactions rather than decomposition to O2. This is expected to have a doubly negative impact on the beer.

Some tasting in the next 4-6 weeks will hopefully provide further information on the degree of oxidation and yeast health experienced in all the samples.

I think future work will definitely be focussing some attention on the starter - in say a split batch of schwarzbier with both starters on stirplates. We'll then hopefully see if there is a positive or negative impact to an aerated starter... and then after that I promise I'll buy an O2 kit.
 
Just wondering, did you have a chance to perform any sensory evaluation on the samples yet?

BTW: I think I'm going to pull the trigger on an O2 kit in the next day or two. Got a lager (Cerny Pivo) I want for Christmas, so not about to take too many risks tying up my single bucket fermentation fridge.
 
I may post my final results here in a few months time, when my oxidation results (for what they're worth) are in..

Forgive my posting this in two threads, but as Adr_0 started this more relevant thread prior to our initial posts in the O2 thread. So because the sensory tests as to whether the beer would last for the long term, being my main focus, I did not complete the H2O2 experiment until a couple of weeks ago when the final two beers were compared. I initially wanted to do a comparison every 2 weeks, but that started to drag out to every month or so (with the remaining beers being consumed in between!

This will be my last post about the H2O2 experiment, as all the bottles are finished. All up, I found that about 6 of the H2O2 bottles showed signs of oxidation, with one friend describing it as tasting like cardboard (I found it tasted like a weird shandy, but not in a nice way). Only one of the aerated bottles (from 25L) showed a similar flavour, which I put down to oxidising from bottling. So 6 from the entire 25L batch 'oxygenated' by H2O2 were less than good. All the others were fairly good and to top things off, after the last few raised the total pf oxidised up to the 6, the very last one was great. So, the older they got the more the oxidation showed (roughly between 3 and 7 months, with most in the 5-7 month period).

All up the aerated batch tasted better all through, with the H2O2 being more hit and miss. I think this does indicate that, for me at least, the idea was good, but the randomness of the O- factor defecting your beers, is just not worth it.

H2O2 as a ghetto oxygenation method. Nah, you're better off aerating.
 
Just wondering, did you have a chance to perform any sensory evaluation on the samples yet?

BTW: I think I'm going to pull the trigger on an O2 kit in the next day or two. Got a lager (Cerny Pivo) I want for Christmas, so not about to take too many risks tying up my single bucket fermentation fridge.
The control and 1 tasted identical, to be honest both were only 'ok' as they were a bit dry. Number two ended up with an aceto infection, while number 3 was flat (flavour wise) and interestingly had basically no head retention - very much an odd occurrence with my beers.

I still need to do a starter comparison in the near future, but in the meantime my oxygenation method has been vitality starters - working an absolute treat in combination with decent cell count. Who'da thunk it?

PS - I still have not bought an oxygenation kit and at this stage do not intend to.
 
Back
Top