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Analytical Chemistry Forum | Forum profile
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Forum profile page for Analytical Chemistry Forum on http://www.chemicalforums.com.
This report page is the aggregated overview from a single forum: Analytical Chemistry Forum, located on the Message Board at http://www.chemicalforums.com.
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Posting activity on Analytical Chemistry Forum:
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Analytical Chemistry Forum Posting activity graph:
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Top authors during last week:
user's latest post:
extraction
Published (2009-11-23 11:04:00)
Quote from: machozitatu on Today at 09:15:44 AM I calculated it out and got 3.5 for X. so that means that 3.5ml of the solute is extracted initially or is that 3.5 mmol extracted. so for the next extraction I would start with 26.5ml and do the same thing (since 30-3.5 is 26.5). If the answer you got was 3.5, then that would be 3.5 mmol extracted, and so 26.5 mmol left in the organic to plug into a second iteration of the equation. Note that I...
user's latest post:
pH of two compounds in water
Published (2009-11-26 14:22:00)
calculate the pH of the solution prepared by adding .10mol each of hydroxylamine and hydrochloric acid in 500ml of water. I was trying to set this up and my understanding is that these two compounds are in water and are "reacting" together to form hydroxylamine hydrochloric acid. with that said the OH in the product would be the determining factor for pH. so would I use the Ka of hydrochloric acid to find OH and then find pH...
user's latest post:
How to calculate calcium content...
Published (2009-11-29 04:10:00)
I can't see where dilution factor comes into play. If you know volume and concentration of EDTA you can calculate number of moles of calcium in the sample - and knowing your sample was 10 mL you can easily calculate mass of calcium per 100 mL. Volume of the sample after NaOH and water were added is irrelevant.
user's latest post:
uv/vis spectroscopy or aa...
Published (2009-11-27 05:24:00)
Depending on Levels, AAS, ICP-AES and ICP-MS, seem to be the accepted techniques at the moment.
user's latest post:
Why would current decrease with...
Published (2009-11-28 03:04:00)
I did think, at one point, that there was some kind of organic 'iron absorber' within the matrix. But then I said it was improbable that some organic species of significant concentrations would ionize itself and respond to exactly the same potential as Fe(III). It's not something I would rule out... but because this signal is the representation of an oxidized species, it's hard to imagine...
user's latest post:
indicator for pb
Published (2009-11-22 18:51:00)
Quote from: IndieSci on Yesterday at 03:49:57 PM Lead chloride is slightly soluble, and I think he is probably working on very dilute solutions so this probably wont work. Yeah, that's what I'm not understanding. If it is high concentration of lead the precipitate will be obvious...if not, it won't be near as obvious or able to be seen at all.
user's latest post:
2 Ultra hard questions left...
Published (2009-11-27 09:11:00)
Ok well I can describe my attempts for #10, I don't know much about 11... I would scan what I did, but I'll try and describe the gist of it. For #10, I plotted absorbance with the fraction. It pretty much looked like a plot of 2 points with the given values. I can't think of what else to do after that...I tried using Nerst equation/stuff outlined in the original question to solve for the fraction, but I'm...
user's latest post:
indicator for pb
Published (2009-11-22 10:53:00)
Hi i work on titration of pb using Xylenol Orange tetrasodium salt indicator for metal titration. if any one he have idea about other indicator may i can use it instead . because its difficult for me to find this one. thank you in advance for further information will be ready. Ash
user's latest post:
indicator for pb
Published (2009-11-22 15:49:00)
Lead chloride is slightly soluble, and I think he is probably working on very dilute solutions so this probably wont work.
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Latest active threads on Analytical Chemistry Forum::
Started 16 hours, 56 minutes ago (2009-12-02 02:59:00)
by sjb
Presumably if you didn't have an acetyl group on there, you'd just have a hydrogen, and the difference between CH 3 CO and H is 43 - 1 = 42?
Started 19 hours, 24 minutes ago (2009-12-02 00:31:00)
by Med90
http://ionsource.com/tutorial/chromatography/rphpl c.htm
Started 3 days, 15 hours ago (2009-11-29 04:10:00)
by Borek
I can't see where dilution factor comes into play. If you know volume and concentration of EDTA you can calculate number of moles of calcium in the sample - and knowing your sample was 10 mL you can easily calculate mass of calcium per 100 mL. Volume of the sample after NaOH and water were added is irrelevant.
Started 4 days, 22 hours ago (2009-11-27 20:58:00)
by Borek
Quote from: bboorriinnggg on Today at 07:45:00 PM So I'm trying to identify a metal in 25 mLs of raspberry juice (hand-crushed) + a bit of KCl, and after running it on CV ultimately yielded unreadable results Does it mean solution is full of organic compounds? Quote I concluded that one of these peaks were iron (nevermind how I came to that conclusion). It matters - data behind your ...
Started 5 days, 14 hours ago (2009-11-27 05:24:00)
by JGK
Depending on Levels, AAS, ICP-AES and ICP-MS, seem to be the accepted techniques at the moment.
Started 5 days, 14 hours ago (2009-11-27 05:17:00)
by JGK
rules is rules, you need to show your attempts first
Started 5 days, 23 hours ago (2009-11-26 20:51:00)
by AWK
Both compounds react to form salt. Since hydroxylamine is a wek base this sult undergoes hydrolysis. You need Ka or Kb of hydroxylamine for pH calculation.
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Hot threads for last week on Analytical Chemistry Forum::
Started 4 days, 22 hours ago (2009-11-27 20:58:00)
by Borek
Quote from: bboorriinnggg on Today at 07:45:00 PM So I'm trying to identify a metal in 25 mLs of raspberry juice (hand-crushed) + a bit of KCl, and after running it on CV ultimately yielded unreadable results Does it mean solution is full of organic compounds? Quote I concluded that one of these peaks were iron (nevermind how I came to that conclusion). It matters - data behind your ...
Started 16 hours, 56 minutes ago (2009-12-02 02:59:00)
by sjb
Presumably if you didn't have an acetyl group on there, you'd just have a hydrogen, and the difference between CH 3 CO and H is 43 - 1 = 42?
Started 5 days, 14 hours ago (2009-11-27 05:24:00)
by JGK
Depending on Levels, AAS, ICP-AES and ICP-MS, seem to be the accepted techniques at the moment.
Started 5 days, 14 hours ago (2009-11-27 05:17:00)
by JGK
rules is rules, you need to show your attempts first
Started 1 week, 1 day ago (2009-11-24 14:49:00)
by renge ishyo
Your way of handling the situation was fine. The key to getting a more accurate determination of the melting point is to increase the temperature on the apparatus *very* slowly, so that you are allowing the apparatus to reach equilibrium at the new temperature before raising the temperature by a very little amount again, etc. etc. until the melting has been complete. If instead you are ramping up...
Started 5 days, 23 hours ago (2009-11-26 20:51:00)
by AWK
Both compounds react to form salt. Since hydroxylamine is a wek base this sult undergoes hydrolysis. You need Ka or Kb of hydroxylamine for pH calculation.
Started 3 days, 15 hours ago (2009-11-29 04:10:00)
by Borek
I can't see where dilution factor comes into play. If you know volume and concentration of EDTA you can calculate number of moles of calcium in the sample - and knowing your sample was 10 mL you can easily calculate mass of calcium per 100 mL. Volume of the sample after NaOH and water were added is irrelevant.
Started 19 hours, 24 minutes ago (2009-12-02 00:31:00)
by Med90
http://ionsource.com/tutorial/chromatography/rphpl c.htm
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