Hello.. Is there any relation between free fatty acid and peroxide value?? Means if i get Free Fatty Acid high then should i get peroxide value also high?? Plz relpy
Thanks for this great video! Can you explain how standardized the preparade 0.01N sodium thiosulpate solution with potassium dicromate. How much we need to add?
May I know thr effecta of Acetic Acid, Potassium Iodide, Water, and Starch soluble in the solution? Also, is the measurement of the reagents added in the solution should be accurate and in order? Thank you.
Thanks for your efforts, please can you explain that high value? You know that the value of oil peroxide must be on range from 0.6 to 0.7 in final product , l did the experiment but the value was very high!!!
Thank you for ypour video, i need to check peroxide value in macadamia nuts. Do i have to extract the oil from them or i can grind them into poweder and then add distilled water or (what chemical can be added to extract) and shake. which is the easier way. If i have to extract oil which is the method? Thank you
If you extract the oil from your sample and do the analysis then it would generate more accurate test results. You can extract the oil by the method of fat extraction using n-Hexane or petroleum ether
Was very clear and a nice explanation...Thank you😊 Can you please clarify my doubt regarding how to standardize the prepared solution of sodium thiosulphate with potassium dichromate...Plz🙏
hello, please can you tell me if i can use this method if i have a really small amount of fat (extracted from a muscle), if not can you recommend me a better method to determine the peroxide value. thank you.
Irfan Ali, you can find FFA from acid value of an oil sample and Acid Value determination procedure is already uploaded. We will upload Rencidity determination procedure very soon. Thank you for being with us.
MicroChem's Experiments do you have details on how create citric acid sulotion for physical degumming. Let say i have 1L of coconut oil how much citric acid and water to mix to perform degumming.
To test a food sample, you have to extract fat or oil content from your food sample first, following our video: ua-cam.com/video/24qWVLm7hhw/v-deo.html After extraction of Fat or oil, use the extracted fat/oil to test for peroxide value by following this video.
@@MicroChemsExperiments ok thank u..I know about the soxhlet extraction process. Since it is a lenghty process iam looking for any alternative method ...plz do let me know if an other .tq
Ajforeversmiley, Possible two reasons for no color change after adding 1% starch are given below: 1. May be the starch solution is not freshly prepared. 2. May be your sample have very low peroxide value.
@@islascel2652 No, we can not say directly that starch powder is spoiled if color does not changed. when we add starch solution, amylose forms a blue to black solution with iodine. So if your sample does not contain iodine then black color will not be formed. The peroxide value is determined by measuring the amount of iodine which is formed by the reaction of peroxides (formed in fat or oil) with iodide ion. So, if color does not changed, interpret the Peroxide value result as 'Nil'
Thanks a lot for making video on this reaction. For few mineral oil we check we didnt get yellow colour after add of ki.so we consider it as a nil. U hv used conc acetic acid. We use diluted as per our sop borrowed fm renowned customer. Will it make diff huge diff.
I am using olive oil, and since chloroform is not available in my school, can I use dichloromethane as a solvent instead of the chloroform-acetic acid mixture?
Do you need a blank titration too for the analysis? Some people do a separate titration for the blank sample. Then subtract the titre value of the blank from the sample(Vs-Vb). Before putting that value into the calculation
Is it inappropriate to stop titration when the solution's top part turns into white?? not the whole part. In our lab, we stop titration when the top part turns into white.. I want to know is there any difference between these two methods.
Hello mam.. I wanted to know if i had to calculate the peroxide value of meat sample.. Is it that i had to extract the fat using soxhlet method and to that extracted fat only i can go for checking peroxide value... Cant i homogenise the meat samlpe directly in water and check the peroxide value of the homogenised sample..
Does it matter if I add the thiosulfate while stirring or not? When I add thiosulfate and wait a little bit versus when I add it while stirring, it yields 2 different results. I am not sure which is right. Please help me explain. thanks
You didnt proformed this procedure accroding to AOAC method. you must titrate the oil after adding the potassium iodide to remove yellow color and then add the starch solution then again titrate to remove bluish color
@@trucminguyen9510 in my lab we titrate the blank the same as the sample, except that there’s no oil added. Blank reading less than 0.05ml is acceptable in my lab.
@@kimmytran9973 hi, may I know how your side prepare the blank? I did follow the method but my blank always end up higher than 0.10, often I get around 0.30 to 0.70ml which is quite high. The procedure I use is as follow: 1) 50ml acetic acid/isooctane into 250ml flask 2) add 30ml reagent water, swirl to mix and add 1ml saturated KI 3) Add 0.50ml starch (blue colour appears) and titrate to endpoint (white). What would cause my blank to be so high? I did prepare new starch and new KI solution but still can't get low blank
I am facing the problem related to Indicator. When I add 1% starch indicator ,No Color change observe. Can you please resolve this issue OR give any suggestion?
In large volume of solution, the color of the end point of the titration is more easier to be seen. Water is added to increase the volume of the solution
Thanks for asking tha question but we have only concern with the experiments, relating our videos. We have no idea about questionnaire and we are very sorry for that.
No. Not enough. Peroxide value just gives an primary indication of Rancidity. You must go for the rancidity test to confirm. We have recently uploaded Rancidity test video. Plzz follow that video for details about rancidity test.
Hello Miss, please I wanna know the average of peroxide value that we can get in our experiment for known is the oil have a good quality or not and thanks in advance.
I have another question about the blank, when I use a blank in this experiment and start my titration on it With thiosulfate of sodium what's the value shall I get when my blank pass to a colorful solution to a colorless solution.
@@29moch.syarifbisma.a6 Volatile compounds are form in the flask afrer mixing the chemicals with samples. Cap should be used to avoid the escape of the volatile matter from the flask.
Dear, Mam. I prepared Sodium thiosulphate (0.01N) solution using your formula and tried to determine the peroxide value.But Blue color of the final mixture is not changing even after adding more than 100 ml (Na2S2O3.5H2O). Then my prepared soln even is not working during standardization of sodium thyosulphate by K2Cr2o7. Where is the problem mam,Is there any problem in Na2s203.5H2O solid.
Yes. May be there is a problem with your sodium thiosulfate crystal. It should not be happened what you said. Otherwise there is problem in glassware and apparatus cleaning. Plzz watch the video again and do the experiment again using clean glassware and apparatus and preparing chemicals and reagents accurately & freshly. After that let us know the result. We will try to find the problem and give you a solution.
@@MicroChemsExperimentsi tried and still trying to solve the problem. I cleaned my apparatus using 32% HCL, then washed several times with Distilled water and dried using hot plate and the burette was rinsed by the sodium thyosulphate solution. Using your video I determined acid value successfully but in determining peroxide value it is not working. I used freshly prepared KI and starch indicator and as the solution turns to blue implies that both KI and starch indicator are in good condition but problem crops up when using sodium thyosulphate. So where is the problem.
@@rashibhasan873 Test another sample brought from local market and test again. If your problm is not solved then replace sodium thiosulfate reagent by a new one of good brand & supplier.
@@MicroChemsExperiments I conducted the experiment several times but it is not working.I am currently using sodium thyosulphate pellets imported from Merck specialities Private Ltd, Worli, India. Which brand should I use instead to get over this problem?
@@SwhyBe Yes. You can purchase 0.01N solution from local market and can use in this experiment. If you face any difficulty to purchase they follow our video for the preparation and standardization: ua-cam.com/video/X2KrBfnKw24/v-deo.html
Thank you for this video. As per ISO and FSSAI manual, there is a step "Titrate with 0.1 N sodium thiosulphate solution with constant and vigorous shaking. Continue titration until the yellow colour almost disappears. Add 0.5 ml of starch solution and continue titration till the blue colour just disappears." AOAC has also mentioned the same. But most of the industries also don't follow this step. They generally do titration directly after adding starch indicator. You also did not followed this step in video. Can you please give some clarity on this?
The type of the titration is two steps titration, so it should be completed separately in two steps to get the more accurate results as suggested by AOAC.
I am doing a PhD in oil quality and I found this video very interesting. Thank you very much, you are great!
Glad it was helpful!
Hello..
Have your Facebook account available?
I want a procedure for preparation of 0.5 N alcoholic KOH
ua-cam.com/video/iALYlxEmNEY/v-deo.html
Dear Mario Vendrell
Your are doing good.
It's my channel, hopefully, my videos will also helpfull to you. Thank u
This video was very clear and help full. Thank you for the effort👍🏻
You are welcome
Thanks I have my practical exam and this helped a ton!
Great to hear!
Very nice description!!!
I have watched the whole video
Also good presentation
Keep it up!!!!!
Maryam Nisar, thank you very much. Many upcoming videos are waiting for you. Be with us.
Keep it up
Doing great 👍
And thanks for vedios
Thanks
Please keep going, this is really helpful
You can add the use of test for beginners so they can know immediately...thank you...good experiment channel keep going
NUTHAKKI RAJESH, thank you for your comment. Surely we will add uses of the test in the video description. Keep supporting us.
Good video guys keep growing
Thanks. Stay with us
Super . Your effort is nice and best hard working . Thank you
Thank you
Hi, how do we calculate the normality of sodium thiosulphate? Thank you for this very informational video.
ua-cam.com/video/X2KrBfnKw24/v-deo.html
Yes but confusing me between 0.1 N thiosulphate and 0.01 N thiosulphate
Plz tell me how to make 0.01N and standardize.
Hello.. Is there any relation between free fatty acid and peroxide value?? Means if i get Free Fatty Acid high then should i get peroxide value also high?? Plz relpy
I suggest to do peroxide value analysis in safety cabinet
Thanks for this great video! Can you explain how standardized the preparade 0.01N sodium thiosulpate solution with potassium dicromate. How much we need to add?
Follow this video: ua-cam.com/video/X2KrBfnKw24/v-deo.html
Great video and helpme a lot, and so ¿This techique work for oils of animal origin? thanks!!
Yes
Good explain sir thank you sir
Thank you. Stay with us
Excuse me, doses the standarisation very important ?
May I know thr effecta of Acetic Acid, Potassium Iodide, Water, and Starch soluble in the solution? Also, is the measurement of the reagents added in the solution should be accurate and in order? Thank you.
Hi. Thanks for the great video! Could you inform me why we have to use acetic acid-chloroform solution but not other solutions ?
AOAC method said so. We will make video later explaining the mechanism of chemical reactions.
nice work
Rahul Pawara, Thank you.
thanks, it is very helpful.
thanks for the great video
can we also calculate tocopherols by this titration method ?
Thanks for your efforts, please can you explain that high value? You know that the value of oil peroxide must be on range from 0.6 to 0.7 in final product , l did the experiment but the value was very high!!!
High peroxide valo means low quality oil or very rancid oil. The oil that has been degraded its component.
@@MicroChemsExperiments thank you so much 😍🥰
Thank you for ypour video, i need to check peroxide value in macadamia nuts. Do i have to extract the oil from them or i can grind them into poweder and then add distilled water or (what chemical can be added to extract) and shake. which is the easier way. If i have to extract oil which is the method? Thank you
If you extract the oil from your sample and do the analysis then it would generate more accurate test results. You can extract the oil by the method of fat extraction using n-Hexane or petroleum ether
Hello,
Thanks for the video it was very informative
I want to know whether this method is useful for excipient study?
Yes. Useful
Was very clear and a nice explanation...Thank you😊
Can you please clarify my doubt regarding how to standardize the prepared solution of sodium thiosulphate with potassium dichromate...Plz🙏
Already uploaded in another video. Please find it in this channel
After adding Saturated KI solution may need to insert corck immediately?
Yes
You are not showing that.
@@newsofislam1284 That was our error occurred to make the video faster. But you should follow what you said in your lab
Thanks a lot.
Very helpful
Thank you
we are getting a high titration value for blank comparing to sample. what should be possible issue in our method?
Thank u👏Where did that 1000 in the calculation come from?
Calculation factor
@@MicroChemsExperiments How can we find that?
hello, please can you tell me if i can use this method if i have a really small amount of fat (extracted from a muscle), if not can you recommend me a better method to determine the peroxide value. thank you.
Miss kindly share rencidity and FFA testing procedure of shortening. Thanks.
Irfan Ali, you can find FFA from acid value of an oil sample and Acid Value determination procedure is already uploaded. We will upload Rencidity determination procedure very soon. Thank you for being with us.
What if the sample is expected to contain iodine? Would this protocol still be applicable since it is using KI as a reagent? Thank you.
Yes. Same protocol should be followed
You are great😂❤❤❤
Thank you
Plz tall me what is 26.5 . Because you did just one time titration
For acetic acid, can you also use the acetic acid you use in the kitchen?
No. The acetic acid in your kitchen is in food grade quality. In analytical laboratory, always use analytical grade of chemicals.
Thank you for sharing this information.
Norman Guanizo, you are welcome
MicroChem's Experiments do you have details on how create citric acid sulotion for physical degumming. Let say i have 1L of coconut oil how much citric acid and water to mix to perform degumming.
For oils we can use sample directly for analysis.. But could u please tell me how to test a food sample ..any digestion process is required??
To test a food sample, you have to extract fat or oil content from your food sample first, following our video: ua-cam.com/video/24qWVLm7hhw/v-deo.html
After extraction of Fat or oil, use the extracted fat/oil to test for peroxide value by following this video.
@@MicroChemsExperiments ok thank u..I know about the soxhlet extraction process. Since it is a lenghty process iam looking for any alternative method ...plz do let me know if an other .tq
@@hafezquadri2972 No other method known to me except extraction of fat
Hola, buenas tardes.
Podría aclararme una duda que tengo?
Yes. Sure. Write us at mail.mic.chem@gmail.com
Dear sir/mam please make the video of dailation test of vanaspati ghee
Will try
Can you please do how to check p anisidine value in oil
When I add the 1% starch solution, there is no colour change. What am I doing wrong?
Ajforeversmiley, Possible two reasons for no color change after adding 1% starch are given below:
1. May be the starch solution is not freshly prepared.
2. May be your sample have very low peroxide value.
@@MicroChemsExperiments If the color does not change even though I prepared it fresh, is the starch powder I use spoiled?
@@islascel2652 No, we can not say directly that starch powder is spoiled if color does not changed. when we add starch solution, amylose forms a blue to black solution with iodine. So if your sample does not contain iodine then black color will not be formed.
The peroxide value is determined by measuring the amount of iodine which is formed by the reaction of peroxides (formed in fat or oil) with iodide ion.
So, if color does not changed, interpret the Peroxide value result as 'Nil'
You could try heating the starch solution before adding it. Worked for me
@@MicroChemsExperiments Btw
When i added Starch first before Distilled water, the black/blue colour is appear
Is that true?
Thanks for the great video! Could you please give the different chemical reaction equations for each step? Thanks.
Great suggestion! Soon
Thanks a lot for making video on this reaction.
For few mineral oil we check we didnt get yellow colour after add of ki.so we consider it as a nil.
U hv used conc acetic acid.
We use diluted as per our sop borrowed fm renowned customer.
Will it make diff huge diff.
You should use concentrated acetic acid as said in AOAC.
I am using olive oil, and since chloroform is not available in my school, can I use dichloromethane as a solvent instead of the chloroform-acetic acid mixture?
Never find any reference of using dichloromethane. So, no idea
Should you do the plank experience? If so, how?
The question is not relevant to the video
May I know what is we don’t add 30ml of dw what will happen
Do you need a blank titration too for the analysis? Some people do a separate titration for the blank sample. Then subtract the titre value of the blank from the sample(Vs-Vb). Before putting that value into the calculation
Yes. you can conduct blank titration to get the more accurate result. But without blank titration you can also get a acceptable result.
Should the blank give a higher or lower titre value?
Is there any replacement for chloroform can dichloromethane be used in place of chloroform?
Not sure and no replacement to be known actually.
Can you use acetic acid / Isooctane, instead of the chloroform? And this and all your videos are very HELPFUL!! Thank you!
Thank you so much for your comment.
No, you can't use any other chemical replacing the chloroform in this test.
Yes.. For safety reason, they allow to use isooctane in replace of chloroform
Is it inappropriate to stop titration when the solution's top part turns into white?? not the whole part. In our lab, we stop titration when the top part turns into white.. I want to know is there any difference between these two methods.
I read you can use cyclohexane for the organic solvent instead of chloroform. Is that true?
CYCLOHEXANE DOES INFACT WORK. YOU NEED TO PIT IN 3 GRAMS OF SAMPLE, 50ML ORGANIC SOLVENT AND 100ML WATER 🔥
Yup
Which type of starch is use as an indicator?
It available as rice, potato and other starch. Can you please specifies its type?
Use reagent grade starch which is soluble in warm water
Can I measure the Peroxide Value while the oil is still hot?
Thank you for the great video by the way!
Yes. You can.
Thanks for making this video
Can you prepare ' oxidation value of oil' video ?
@@souravsarkar4497 You are welcome. Noted the parameter. We will work on it.
@@MicroChemsExperiments i couldn't get this video
@@souravsarkar4497 Why? Which part of this video is not understandable to you? I think it's a clearly explained video.
@@MicroChemsExperiments i want to know oxidation value of oil and fat
Hello mam.. I wanted to know if i had to calculate the peroxide value of meat sample.. Is it that i had to extract the fat using soxhlet method and to that extracted fat only i can go for checking peroxide value...
Cant i homogenise the meat samlpe directly in water and check the peroxide value of the homogenised sample..
You can check peroxide Value directly using the blended meat sample.
What standard peroxide value ??
Does it matter if I add the thiosulfate while stirring or not? When I add thiosulfate and wait a little bit versus when I add it while stirring, it yields 2 different results. I am not sure which is right. Please help me explain. thanks
Add thiosulfate while stirring
How fast should I add it?
You didnt proformed this procedure accroding to AOAC method. you must titrate the oil after adding the potassium iodide to remove yellow color and then add the starch solution then again titrate to remove bluish color
Please help me explain, In this test, do we need to titrate the blanc sample?
This video are very helpfull, thank you so much.
Yes. We need to tritrate our sample after dissolving in ethanol by heating.
@@MicroChemsExperiments how to titrate the blanc sample? Can i change sample test to distill water
@@trucminguyen9510 in my lab we titrate the blank the same as the sample, except that there’s no oil added. Blank reading less than 0.05ml is acceptable in my lab.
@@kimmytran9973 thank you so much
@@kimmytran9973 hi, may I know how your side prepare the blank? I did follow the method but my blank always end up higher than 0.10, often I get around 0.30 to 0.70ml which is quite high. The procedure I use is as follow:
1) 50ml acetic acid/isooctane into 250ml flask
2) add 30ml reagent water, swirl to mix and add 1ml saturated KI
3) Add 0.50ml starch (blue colour appears) and titrate to endpoint (white).
What would cause my blank to be so high? I did prepare new starch and new KI solution but still can't get low blank
Wow this video is really helpful for me thanks❤!! Can I know why the unit is in per kg, when we use our oil sample in gram for the calculation though?
Look at the calculation again. It was multiplied by 1000 to covert the value into Kg.
Range of peroxide value in soyabean refined oil ????
Take reference of ranges using Google
Blue colour not appear after adding starch solution
Can i do this experiment with maize parts
No idea. You can try
I am facing the problem related to Indicator.
When I add 1% starch indicator ,No Color change observe.
Can you please resolve this issue OR give any suggestion?
As I use freshly prepare KI and Starch Indicator.
Why you add .02g Sodium carbonate in Sodium thiosulfate solution ?
AOAC method said so
Can we use for titration 0.1 n sodium thiosulfate
No. If you use 0.1N instead of 0.01N then you will not get the accurate result of peroxide value.
For sodium thiosulfate I found supplier that sell this solution and its standard already ? Do I need to standardise it after opening?
No need to standardise again.
Can you use this method to determine peroxide value in dried milk powder?
Yes. You can
@@MicroChemsExperiments Great thank you so much! Do I need to extract fat from the powder first or the method can be applied to milk powder directly?
You have to extract fat first using Hexane or Ether solvent. Then go for the analysis
Sorry, why must add 30 mL distilled water and shake 1 min to mix ?
I would thank you very much😢
In large volume of solution, the color of the end point of the titration is more easier to be seen. Water is added to increase the volume of the solution
0.5 g starch soluble added in how much ml of water?
50 ml
What research question can be formed out of this experiment for IB experiment?
Thanks for asking tha question but we have only concern with the experiments, relating our videos. We have no idea about questionnaire and we are very sorry for that.
Is peroxide value test enough to check if the oil is rancid or not?
No. Not enough. Peroxide value just gives an primary indication of Rancidity. You must go for the rancidity test to confirm. We have recently uploaded Rancidity test video. Plzz follow that video for details about rancidity test.
Hello Miss, please I wanna know the average of peroxide value that we can get in our experiment for known is the oil have a good quality or not and thanks in advance.
Lower peroxide value indicates the good quality of oil. Quality decreases with the increasing peroxide value.
Thank you so much 🥰
I have another question about the blank, when I use a blank in this experiment and start my titration on it With thiosulfate of sodium what's the value shall I get when my blank pass to a colorful solution to a colorless solution.
@@oumaimaazakak7285 It varies with many conditions or parameters. Plz conduct the test in your lab to get the more idea.
How to prepare wijs reagent using ICl
We will make video later. Till then, purchase prepared wij's solution
But at least tell me the procedure
is it necessary to shake the sample with potassium iodide in dark conditions or this is has no influence on analysis.
You dont need to keep the sample in dark after adding KI solution.
thank you so much for this video
You are most welcome.
Which AOAC method is the reference for this?
Reference is given in the video title
@@MicroChemsExperiments oh yeah! Sorry I missed that! Thank you
@@MrLongKR no problem sir. Thank you
My teacher asked what is the relationship between cloud point and melting point do u know?
Take help from Google
In my Lab. While shake/mix The Erlen must be Close with Tube for erlenmeyer
Is that True?:/
Yes. True
@@MicroChemsExperiments can you give me the reason, why we do that? :/
@@29moch.syarifbisma.a6 Volatile compounds are form in the flask afrer mixing the chemicals with samples. Cap should be used to avoid the escape of the volatile matter from the flask.
@@MicroChemsExperiments oh ok, thank you :D
@@29moch.syarifbisma.a6 You are welcome
Thank you!
It's our pleasure. Stay with us.
Can you give me the "Determination of Oil Analysis" manual if I need it?
We do not provide any document
I tried this one but when I added starch solution, no blue or black colour produced. What is the reason for that?
Prepare your reagents freshly and try again. If same result found, you can interpret the result as 'Nil'
Why did you add sodium carbonate?
Standardization method said so
Why when i put starch the sample not turning blue/ black it just white
Prepare chemicals freshly and try again
I have tested body oil of brand and peroxide value is 34 does that mean is not good in quality ?
Yes. Not good in quality of that oil
How to standardize sodium thiosulfate by patassium dichromate?
Link: ua-cam.com/video/X2KrBfnKw24/v-deo.html
Did you watch my video list. Please search your asking test from my video list.
Pls make the video of preparation & standardization 0.1 N/M of Potassium Dichromatte
Ok. We will make. Please stay with us
Lovely
Pranay Sarkar, Thank you so much. Be with us.
Dear, Mam. I prepared Sodium thiosulphate (0.01N) solution using your formula and tried to determine the peroxide value.But Blue color of the final mixture is not changing even after adding more than 100 ml (Na2S2O3.5H2O). Then my prepared soln even is not working during standardization of sodium thyosulphate by K2Cr2o7. Where is the problem mam,Is there any problem in Na2s203.5H2O solid.
Yes. May be there is a problem with your sodium thiosulfate crystal. It should not be happened what you said. Otherwise there is problem in glassware and apparatus cleaning. Plzz watch the video again and do the experiment again using clean glassware and apparatus and preparing chemicals and reagents accurately & freshly. After that let us know the result. We will try to find the problem and give you a solution.
@@MicroChemsExperimentsi tried and still trying to solve the problem. I cleaned my apparatus using 32% HCL, then washed several times with Distilled water and dried using hot plate and the burette was rinsed by the sodium thyosulphate solution. Using your video I determined acid value successfully but in determining peroxide value it is not working. I used freshly prepared KI and starch indicator and as the solution turns to blue implies that both KI and starch indicator are in good condition but problem crops up when using sodium thyosulphate. So where is the problem.
@@rashibhasan873 Test another sample brought from local market and test again. If your problm is not solved then replace sodium thiosulfate reagent by a new one of good brand & supplier.
@@MicroChemsExperiments I conducted the experiment several times but it is not working.I am currently using sodium thyosulphate pellets imported from Merck specialities Private Ltd, Worli, India. Which brand should I use instead to get over this problem?
@@rashibhasan873 before changing the chemicals, conduct a test for another saybean oil sample purchased from the local market.
thanks a million
You are most welcome. Stay with us.
Great video can please mention the concentration % of acetic acid
We used Glacial Acetic Acid (99.5%)
@@MicroChemsExperiments perfect one more question can I purchase 0.0109N solution already prepared and standardised will it work for this experiment?
@@SwhyBe Yes. You can purchase 0.01N solution from local market and can use in this experiment.
If you face any difficulty to purchase they follow our video for the preparation and standardization: ua-cam.com/video/X2KrBfnKw24/v-deo.html
@@MicroChemsExperiments its not 0.01N actually it is 0.0109 N will this effect the experiment?
@@SwhyBe No problm with it
How many times we should do titration
Just follow the video
please please can you explain how to standardise the sodium thiosulphate
ua-cam.com/video/X2KrBfnKw24/v-deo.html
Sir When I was use starch solution no blue colour observed....
What is the error
Prepare starch solution and potassium iodide solution freshly just before the analysis.
Which starch are used basically Maize Starch or soluble starch
Soluble starch should be used.
But I not get the result
When I m adding starch solutions tha sample colour not turn black colour it will be in yellow (for ghee sample ) give me solutions
Prepare potassium Iodide and Starch solution freshly on the day of analysis.
Super
Thank you
Thank you for this video. As per ISO and FSSAI manual, there is a step "Titrate with 0.1 N sodium thiosulphate solution with constant and vigorous shaking. Continue titration until the yellow colour almost disappears. Add 0.5 ml of starch solution and continue titration till the blue colour just disappears." AOAC has also mentioned the same. But most of the industries also don't follow this step. They generally do titration directly after adding starch indicator. You also did not followed this step in video. Can you please give some clarity on this?
The type of the titration is two steps titration, so it should be completed separately in two steps to get the more accurate results as suggested by AOAC.
The problem is i don't have any of this equipments, even the liquids. Im a student and we need to test the peroxide value of our oil. Help me pls
Contact a laboratory around you
Sir may be most of the oil are not showing blue colour when added the starch solution...
Color depends on the peroxide value of sample. Without blank conduction, you can get the accurate results by following this video.
Total 2percent contain.......so it will show blue or not?