j_sum1
Administrator
Posts: 6324
Registered: 4-10-2014
Location: At home
Member Is Online
Mood: Most of the ducks are in a row
|
|
Easy to obtain standards for titrations and other analytical methods
Good analysis is part and parcel of good chemistry – figuring out what you have got and how much theer is. But qualitatively measuring
concentrations can be painful as an amateur. We are basically limited to 3sf precision in any measuring equipment that we own. We resort to density
measurements to get approximate concentrations of many liquids. And that good old method of titration is hamstrung by the lack of good standard
solutions. (Besides, it can be tedious, time-consuming and require meticulous practice and patience that I, at least, am often lacking.)
With that dismal introduction I propose this thread as a place to share ideas regarding good, reliable standards that are easily accessible to the
amateur. I begin with the following:
Oxalic acid
This can be either the anhydrous or dihydrate or some mix between. But it can be easily dehydrated using toluene and a dean-stark trap or improvised
alternative. The acid itself is strong enough that it makes for ok titrations. I have also heard of people oven-drying OA to get the anhydrous form
or recrystallising from water to obtain the dihydrate but I am not sure of the accuracy of these methods. (I have done reactions with OTC oxalic acid
dihydrate straight out of the box and got quantitative results. Reaction with excess Fe2+ solution to produce and isolate iron oxalate is a great
student experiment for confirming stoichiometry.)
Sodium carbonate
This has numerous hydrated forms so is completely unsuitable out of the box. But it is possible to make good quality anhydrous Na2CO3 by heating
NaHCO3 and liberating H2O and CO2. Oven drying works: 2h at high temperature with occasional stirring. Heating first in a beaker over a flame will
speed up the process and is slightly less messy. (You do get a white film on the inside of the oven.)
Copper sulfate
High purity copper sulfate pentahydrate is easy to get. This is easily decomposed to anhydrous CuSO4 with oven baking: again with stirring. I have
heard of this being used as a standard for redox titration but I forget the details.
Any others?
The past couple of days I have been thinking about this and wondered at the possibility of using pharmaceutical products such as aspirin and vitamin C
tablets which are presumably manufactured with tight tolerances. But I am not sure how reasonable this is.
|
|
|
Sulaiman
International Hazard
Posts: 3697
Registered: 8-2-2015
Location: 3rd rock from the sun
Member Is Offline
|
|
For REDOX,
potassium permanganate is quite pure, and not too expensive,
and can be bought via eBay as >= 99.4% and >=99.9% purity.
relatively cheap and pure iodine and sodium thiosulphate are available via eBay.
_______________________________________________________________
AFAIK, until recently USP weight measurements had classes of accuracy (e.g. 1% and 0.1%) but now USP only requires manufacturers to work to what they
consider suitable accuracy,
which for benign chemicals (e.g. vit.C) could be - not accurate at all.
Qualified pharmaceutical chemists probably know more on this 
[Edited on 29-2-2020 by Sulaiman]
CAUTION : Hobby Chemist, not Professional or even Amateur
|
|
|
Fery
International Hazard
Posts: 1018
Registered: 27-8-2019
Location: Czechoslovakia
Member Is Offline
|
|
Potassium hydrogenphtalate for acidobasic titrations.
Zn metal for EDTA complexometric titrations (must be dissolved in an acid after weighing it of course).
(NH4)2Fe(SO4)2 . 6 H2O for redox titrations
KBrO3 for standardisation of Na2SO3
NaCl for standardisation of AgNO3 (precipitation titration)
|
|
|
Heptylene
Hazard to Others
Posts: 319
Registered: 22-10-2016
Member Is Offline
Mood: No Mood
|
|
Sulfamic acid can be used as a primary standard. See attached pdf for a purification procedure
Attachment: Purification of sodium carbonate and sulfamic acid.pdf (240kB)
This file has been downloaded 343 times
|
|
|
unionised
International Hazard
Posts: 5126
Registered: 1-11-2003
Location: UK
Member Is Offline
Mood: No Mood
|
|
A quick mention for borax and cream of tartar as pH references.
|
|
|
DavidJR
National Hazard
Posts: 908
Registered: 1-1-2018
Location: Scotland
Member Is Offline
Mood: Tired
|
|
In order to use sodium carbonate as a primary standard you really have to oven dry it first even if you have nominally anhydrous material.
|
|
|
clearly_not_atara
International Hazard
Posts: 2789
Registered: 3-11-2013
Member Is Offline
Mood: Big
|
|
Potassium tetraoxalate - KH3(C2O4)2 is easily precipitated from mixtures of almost any soluble potassium salt and oxalic acid. It is
used as a pH calibration standard because it has a low solubility of 2.5% w/w or just about 0.2 molar although the more common solution used is half
that concentration -- 0.1 molar with a pH of 1.7. I think I have a picture of the prep somewhere; you just combine solutions and filter, couldn't be
easier. The dihydrate is stable and non-hygroscopic.
More importantly, because the saturated concentration is low and the protons are all fairly acidic (the last one is lost at about pH 5.5) it can be
used to titrate low concentrations of alkali in conjunction with an indicator.
[Edited on 29-2-2020 by clearly_not_atara]
|
|
|
nezza
Hazard to Others
Posts: 324
Registered: 17-4-2011
Location: UK
Member Is Offline
Mood: phosphorescent
|
|
You can buy volumetric standard acid (HCl) and base (NaOH) as 0.1M solutions on ebay.
If you're not part of the solution, you're part of the precipitate.
|
|
|
Bedlasky
International Hazard
Posts: 1239
Registered: 15-4-2019
Location: Period 5, group 6
Member Is Offline
Mood: Volatile
|
|
For acids:
Anhydrous Na2CO3
NaHCO3 or KHCO3
Borax
Sodium oxalate
For bases:
Oxalic acid
Potassium hydrogenphtalate
Benzoic acid
For manganometry and cerimetry:
Oxalic acid or sodium oxalate
For any reducing agent:
K2Cr2O7
KIO3
For TiCl3, SnCl2 and CrCl2 also NH4Fe(SO4)2.12H2O
For iodine:
Resumblimation
Sodium thiosulfate solution of known concentration (you can make your own and standardize it).
(As2O3 - but this isn't common and it's for experienced chemists)
For chelatometry:
MgSO4.7H2O
ZnSO4.7H2O
Bismuth or copper metal
For argentometry nad mercurymetry:
NaCl
For K4[Fe(CN)6]:
ZnSO4.7H2O
[Edited on 29-2-2020 by Bedlasky]
|
|
|
j_sum1
Administrator
Posts: 6324
Registered: 4-10-2014
Location: At home
Member Is Online
Mood: Most of the ducks are in a row
|
|
Lots of good ideas here. But rather than just a list, I would love procedures for converting otc products or just using them as is.
I did not know about saturated potassium bitartrate as a pH standard. That is cool. Can it also be used as an acid titration standard? It would be
extremely useful for an education project I have if that is the case.
|
|
|
CharlieA
National Hazard
Posts: 646
Registered: 11-8-2015
Location: Missouri, USA
Member Is Offline
Mood: No Mood
|
|
If you use a burette with 0.1 mL divisions, use more than 10 mL of titrant and interpolate between the divisions to the nearest 0.01 mL (using a Mark
I eyeball, aided or unaided), you can get 4 SF. And 3 SF is still 1 part per thousand, which would make even a purist happy (most of the time ). To standardize strong acids/bases, KHP is the best, and making up a liter or so
of each reagent that you have to standardize should last a reasonable time.
The first sentence of your original post is so true! I suspect many posters perform some qualitative/quantitative tests to characterize their
products, but they often don't report that. I'm presently trying to fit a PID + type T thermocouple to an old Fisher-Johns melting point apparatus so
I can dispense with my Thiele tube. Breaking thermometers is annoying and original replacements for the F-J apparatus that I have found are
exorbitantly priced.
|
|
|
Bedlasky
International Hazard
Posts: 1239
Registered: 15-4-2019
Location: Period 5, group 6
Member Is Offline
Mood: Volatile
|
|
Quote: Originally posted by j_sum1  | Lots of good ideas here. But rather than just a list, I would love procedures for converting otc products or just using them as is.
I did not know about saturated potassium bitartrate as a pH standard. That is cool. Can it also be used as an acid titration standard? It would be
extremely useful for an education project I have if that is the case. |
For standardization of acids I often use carbonates/bicarbonates. As indicator I use methyl orange. Titrate your standard with acid
(HCl, H2SO4) and when indicator turns in to the orange, then boil solution to get all of carbon dioxide from solution. Solution turns back to the
yellow. After that let it cool to the room temperature and titrate it again with acid to the pink colour.
Borax have some advantages - higher molar mass, so there is smaller error, and you don't need boil solution, because boric acid is weaker acid than
carbonic and doesn't interfere determination.
For standardization of bases (NaOH, KOH) I use oxalic acid. You can use phenolphtalein or methyl orange as indicators. With
phenophtalein it's very simple titration - end point is when indicator turns in to the pink.
For methyl orange exist different technique. You titrate oxalic acid with hydroxide until indicator turns in to the orange. Then you add 10ml of 20%
CaCl2 - this caused formation of insoluble calcium oxalate and HCl. Solution turns back in to the pink and you titrate it to the yellow colour.
Interesting alternative can be benzoic acid for standardization of KOH in ethanol which can be used for determination of acidity number of oil or for
testing of purity of organic acids. Phenolphtalein is suitable indicator for this.
For standardization of KMnO4 I use oxalic acid. Oxalic acid reacts only slowly with KMnO4, so solution must be hot or instead of
heating you can use MnSO4 as catalyst. Indicator is KMnO4 itself.
For standardization of TiCl3
I never did this, but I plan it with ammonium ferric sulfate as standard. There is two possible indications:
Methylene blue: Until solution turns from blue to colourless
KSCN: Until solution turns from red to colourless
For standardization of Na2S2O3
Potassium dichromate or iodate is dissolved in water, then you add sulfuric acid, excess of KI and let it stand for 10 minutes. Then you titrate this
solution until it turns pale yellow. After that add some starch solution, which forms with iodine dark blue complex. Then titrate it until solutions
turns in to the colourless.
Similar procedure is used for standardization of iodine (without using of oxidizing agent).
For standardization of AgNO3
Simple titration of NaCl with AgNO3 solution. As indicator you can use K2CrO4 (which forms with Ag+ reddish brown precipitate) or fluorescein (end
point is when fluorescence disappear).
For standardization of Hg(NO3)2
Simple titration of NaCl with Hg(NO3)2 solution. As indicator you can use sodium nitroprusside which forms with excess of Hg nitrate white
precipitate.
For standardization of Na2H2EDTA
Simple titration of ZnSO4 or MgSO4. Indicator is eriochrome black T. Titration must be done at pH = 10.
Some procedures are here:
https://www.gitam.edu/departments_cms/assets/uploads/syllabu...
http://egyankosh.ac.in/bitstream/123456789/43339/1/Exp-10.pd...
http://www.titrations.info/
|
|
|
Sulaiman
International Hazard
Posts: 3697
Registered: 8-2-2015
Location: 3rd rock from the sun
Member Is Offline
|
|
| Quote: Originally posted by CharlieA | | If you use a burette with 0.1 mL divisions, use more than 10 mL of titrant and interpolate between the divisions to the nearest 0.01 mL (using a Mark
I eyeball, aided or unaided), you can get 4 SF. And 3 SF is still 1 part per thousand, which would make even a purist happy (most of the time ). |
(from a transiently unhappy metrology purist)
When I do (e.g. acid:base) titrations the limits to accuracy are;
1 the accuracy of the molarity of the titrant
2 titration equivalency may not be pH7
3 equivalency pH determination errors
4 the minimum dispensable quantity is one drop ... typically between .03ml and .05ml
5 my 50ml class-A burettes have 0.1ml divisions and are supposed to be accurate to 0.05ml
6 each drop of titrant adhering to the inner wall of the burette is also about 0.05ml error
7 near 20oC the volumetric thermal expansion of water is about 207 ppm/oC so 5oC error = 0.1% volume error
This is why I find it near impossible to achieve 0.1% absolute accuracy
but fairly easy to maintain 1% accuracy
CAUTION : Hobby Chemist, not Professional or even Amateur
|
|
|
CharlieA
National Hazard
Posts: 646
Registered: 11-8-2015
Location: Missouri, USA
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by Sulaiman | | Quote: Originally posted by CharlieA | | If you use a burette with 0.1 mL divisions, use more than 10 mL of titrant and interpolate between the divisions to the nearest 0.01 mL (using a Mark
I eyeball, aided or unaided), you can get 4 SF. And 3 SF is still 1 part per thousand, which would make even a purist happy (most of the time ). |
(from a transiently unhappy metrology purist)
When I do (e.g. acid:base) titrations the limits to accuracy are;
1 the accuracy of the molarity of the titrant
2 titration equivalency may not be pH7
3 equivalency pH determination errors
4 the minimum dispensable quantity is one drop ... typically between .03ml and .05ml
5 my 50ml class-A burettes have 0.1ml divisions and are supposed to be accurate to 0.05ml
6 each drop of titrant adhering to the inner wall of the burette is also about 0.05ml error
7 near 20oC the volumetric thermal expansion of water is about 207 ppm/oC so 5oC error = 0.1% volume error
This is why I find it near impossible to achieve 0.1% absolute accuracy
but fairly easy to maintain 1% accuracy |
Sulaiman, I am truly impressed with your attention to detail! But since I'm just a retired chemist (I last practiced professionally over 35 years
ago, so now I consider myself an amateur chemist), I would be satisfied with 1% accuracy, but that is just me.
|
|
|
Ubya
International Hazard
Posts: 1247
Registered: 23-11-2017
Location: Rome-Italy
Member Is Offline
Mood: I'm a maddo scientisto!!!
|
|
sulaiman got a point, purity of the standard is not the only thing.
in uni i did a quantitative analytical chemistry class, we used analytical balances (+0.1mg) to weight our standard compounds, dried for 24 hours and
kept always in a desiccator, using 50ml class A burettes with schellbach line for easier identification of the meniscus. we tried to not use
approximate equations (they can get pretty long lol) to minimize mathematical errors. it was my first time using a burette so i wasn't an expert, but
at the end of the lab i did around 35 titrations, being really carefull, slow (the burettes were degreased but still a film of liquid would form on
the walls, a fast dripping rate and a quick look at the level of the solution would give an error, as with time the adhered solution would slowly go
down the wall and reach the top of the meniscus, giving you now a bigger volume. if you are fast you think to have used more solution than what you
actually used) i would still get 1-2% of error minimum. then you have to think that many solutions are not stable, permanganate for example, yea you
can get that pretty pure, but it slowly decomposes in solution.
then there's temperature... and if you don't have air conditioning in your lab to keep everything at a constant temperature, it can be a source of
error (even if not huge most of the time)
---------------------------------------------------------------------
feel free to correct my grammar, or any mistakes i make
---------------------------------------------------------------------
|
|
|
![[*]](images/xpblue/default_icon.gif){kind=icon}
