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Winemaking (rec.crafts.winemaking) Discussion of the process, recipes, tips, techniques and general exchange of lore on the process, methods and history of wine making. Includes traditional grape wines, sparkling wines & champagnes. |
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What would be easier to use and more accurate. A titration kit with a PH
meter or a Acidometer? I don't get the titration kit by itself. I add tons of acid and the color of the wine still changes with only 1cc of sodium hydroxide. |
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Speaking of Acid Tritration, a great frustration for me is determining
the end point when testing reds. Yes, I dilute the wine appropriately. Can someone please give me insight regarding the end point color I should be watching for? A red will gradually turn to a reddish-gray, then a more muddy red-gray, then brown-gray, then green-brown-gray, then dark green (I think the sequence is something like that) over a fairly large volume of NaOH additions. What color do I say "Eureka! It's neutral!"? Thanks, Jim |
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I agree. When I did titration briefly in a commercial lab, I had my sample
on an automatic stirrer with a magnetic stir bar in the flask. Then, I added phelphtptphptphptptptptliiiien :-) until the color lasted for about 5-10 seconds. Having the constant stirring helped make it uniform. If possible, try to "get calibrated". Could you borrow a ph meter? Then you could titrate and compare color to actual values until you calibrate your pink (I loved calling it that). Also, in my case, I had used a Cash Still to separate the volatile acids out. The nice thing about this was that the condensed acidic liquid was always colorless -- made "pinking" a lot easier. Howard (newbie) "Greg Cook" > wrote in message s.com... > On 3/25/04 8:50 AM, in article > , "gus" > > wrote: > > > (glad heart) wrote in message > > . com>... > >> Speaking of Acid Tritration, a great frustration for me is determining > >> the end point when testing reds. Yes, I dilute the wine > >> appropriately. Can someone please give me insight regarding the end > >> point color I should be watching for? A red will gradually turn to a > >> reddish-gray, then a more muddy red-gray, then brown-gray, then > >> green-brown-gray, then dark green (I think the sequence is something > >> like that) over a fairly large volume of NaOH additions. > >> > >> What color do I say "Eureka! It's neutral!"? > >> > >> Thanks, Jim > > > > hey jim, > > i use a titration test and ph meter together. > > > > using a ph meter to check for the end point takes all the guess work > > out of the end point. many on the board have said that the endpoint is > > when you measure a ph of 8.2, however, my bottle of blueing solution > > says to measure to 7.0 so that's what i do. > > > > good luck, > > gus > > > The thing to look for about titration using phenolphthalein is to stop at > the point when adding a drop causes a pink color to remain even after > swirling/mixing your sample well. If you go a few drops past, that's > accurate enough for titration. Of course, this is pretty darn hard with red > wines - as you have noticed. Using a pH meter to titrate would be a > preferred method with reds. Generally we titrate to pH 8.2 because that is > the pH at which phenolphthalein changes color. Thus, it would be consistent > with colorimetric titrations. I think the difference between pH 7 and 8.2 > during the titration is a matter of just a few drops anyway (the titration > curve is very very steep at the point of neutralization of the acids). > -- > Greg Cook > http://homepage.mac.com/gregcook/Wine > > (remove spamblocker from my email) > |
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Stop at the permanent color change.
Can someone please give me insight regarding the end > >> point color I should be watching for? A red will gradually turn to a > >> reddish-gray, The Europeans use 7 as the endpoint, North Americans use 8.2. I have noted it's not that big a difference just as Greg mentioned, the PH really takes off around 7. I use 8.2 > > using a ph meter to check for the end point takes all the guess work > > out of the end point. many on the board have said that the endpoint is > > when you measure a ph of 8.2, however, my bottle of blueing solution > > says to measure to 7.0 so that's what i do. > ....> Using a pH meter to titrate would be a > preferred method with reds. Generally we titrate to pH 8.2 because that is > the pH at which phenolphthalein changes color. Thus, it would be consistent > with colorimetric titrations. I think the difference between pH 7 and 8.2 > during the titration is a matter of just a few drops anyway (the titration > curve is very very steep at the point of neutralization of the acids). |
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I just purchased a PH meter. I got a Hanna Piccolo 2. No more guessing
games for me. "Joe Sallustio" > wrote in message om... > Stop at the permanent color change. > > Can someone please give me insight regarding the end > > >> point color I should be watching for? A red will gradually turn to a > > >> reddish-gray, > > The Europeans use 7 as the endpoint, North Americans use 8.2. I have > noted it's not that big a difference just as Greg mentioned, the PH > really takes off around 7. I use 8.2 > > > > > using a ph meter to check for the end point takes all the guess work > > > out of the end point. many on the board have said that the endpoint is > > > when you measure a ph of 8.2, however, my bottle of blueing solution > > > says to measure to 7.0 so that's what i do. > > > > ...> Using a pH meter to titrate would be a > > preferred method with reds. Generally we titrate to pH 8.2 because that is > > the pH at which phenolphthalein changes color. Thus, it would be consistent > > with colorimetric titrations. I think the difference between pH 7 and 8.2 > > during the titration is a matter of just a few drops anyway (the titration > > curve is very very steep at the point of neutralization of the acids). |
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Thanks for those insights everyone. I can see it's high time to buy a pH meter.
Jim |
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The equivalence point (amount of acid = amount of sodium hydroxyde)
depends on the acids present and their relative amounts. For tartaric acid it will be at about pH=8,5. For malic acid it would be about pH=9,8. In a mixture of acids (wine) it will be very difficult to even find the exact equivalence point even if you obtained the full titration curve, but such a curve will give the best indication. To simplify this a titration standard is used. The exact pH value does not become very important as long as it is in the range 7 - 9. The selected value of pH=8.2 Is probably a practical choice since the commonly used indicator phenolptalein starts its colour shift to red at this point. Why the Europeans selected pH=7 is perhaps because this represent the value for pure water. Strictly all titrations require a correction for the titration error made by using an indicator with colour change at a different pH than the "equivalence" point of the acid(s). For the US standard this error is negligible when using phenoltalein. Greg Cook > wrote in message ws.com>... > On 3/25/04 5:24 PM, in article > , "Joe Sallustio" > > wrote: > > > Stop at the permanent color change. > > > > Can someone please give me insight regarding the end > >>>> point color I should be watching for? A red will gradually turn to a > >>>> reddish-gray, > > > > The Europeans use 7 as the endpoint, North Americans use 8.2. I have > > noted it's not that big a difference just as Greg mentioned, the PH > > really takes off around 7. I use 8.2 > > Yup - I suspect that is because the European standard for TA is based on > Sulfuric Acid (H2SO4) rather than Tartaric Acid. Can anyone enlighten me on > that one? > > Thanks. |
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Greg Cook > wrote:
> I think the difference between pH 7 and 8.2 > during the titration is a matter of just a few drops anyway (the titration > curve is very very steep at the point of neutralization of the acids). Theoretically, that's true and I always assumed there'd be little difference. I haven't done enough comparisons to accurately judge, but I actually just read a paper recently which suggests this difference *is* significant. In the paper [1], they compared the OIV method (titrate to pH 7.0, 50 ml wine) and the AOAC method (titrate to pH 8.2, 10 ml wine diluted with water to 100 ml) for 30 wines. They found no significant difference due to operative technique (i.e. the dilution and sample sizes), but they did find a difference due to pH end-point. This difference correlated to a TA difference of 0.6 g/l (as tartaric) for reds and 0.5 g/l for whites. Well, I consider that significant. BTW, if the standard was to titrate to the actual equivalence point for wines, we'd all be titrating to pH's of around 10. In the purely practical sense, I'm glad we have a standard at pH 7/8.2. Certainly saves on the NaOH ;-) Ben [1] Darias-Martín, J. et al. (2003). Comparative study of methods for determination of titrable acidity in wine. J. Food Composition and Analysis 16, 555-562. |
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On 3/29/04 6:35 PM, in article
, "Ben Rotter" > wrote: > Greg Cook > wrote: > >> I think the difference between pH 7 and 8.2 >> during the titration is a matter of just a few drops anyway (the titration >> curve is very very steep at the point of neutralization of the acids). > > Theoretically, that's true and I always assumed there'd be little > difference. I haven't done enough comparisons to accurately judge, but > I actually just read a paper recently which suggests this difference > *is* significant. > > In the paper [1], they compared the OIV method (titrate to pH 7.0, 50 > ml wine) and the AOAC method (titrate to pH 8.2, 10 ml wine diluted > with water to 100 ml) for 30 wines. They found no significant > difference due to operative technique (i.e. the dilution and sample > sizes), but they did find a difference due to pH end-point. This > difference correlated to a TA difference of 0.6 g/l (as tartaric) for > reds and 0.5 g/l for whites. Well, I consider that significant. > > BTW, if the standard was to titrate to the actual equivalence point > for wines, we'd all be titrating to pH's of around 10. In the purely > practical sense, I'm glad we have a standard at pH 7/8.2. Certainly > saves on the NaOH ;-) > > Ben > > [1] Darias-Martín, J. et al. (2003). Comparative study of methods for > determination of titrable acidity in wine. J. Food Composition and > Analysis 16, 555-562. Ben --- thanks for the reference. This is very interesting. -- Greg Cook http://homepage.mac.com/gregcook/Wine (remove spamblocker from my email) |
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Something in the post and messenger for you?
"Ben Rotter" > wrote in message om... | Greg Cook > wrote: | | > I think the difference between pH 7 and 8.2 | > during the titration is a matter of just a few drops anyway (the titration | > curve is very very steep at the point of neutralization of the acids). | | Theoretically, that's true and I always assumed there'd be little | difference. I haven't done enough comparisons to accurately judge, but | I actually just read a paper recently which suggests this difference | *is* significant. | | In the paper [1], they compared the OIV method (titrate to pH 7.0, 50 | ml wine) and the AOAC method (titrate to pH 8.2, 10 ml wine diluted | with water to 100 ml) for 30 wines. They found no significant | difference due to operative technique (i.e. the dilution and sample | sizes), but they did find a difference due to pH end-point. This | difference correlated to a TA difference of 0.6 g/l (as tartaric) for | reds and 0.5 g/l for whites. Well, I consider that significant. | | BTW, if the standard was to titrate to the actual equivalence point | for wines, we'd all be titrating to pH's of around 10. In the purely | practical sense, I'm glad we have a standard at pH 7/8.2. Certainly | saves on the NaOH ;-) | | Ben | | [1] Darias-Martín, J. et al. (2003). Comparative study of methods for | determination of titrable acidity in wine. J. Food Composition and | Analysis 16, 555-562. |
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