HI Joe
Saturate it with salt - with salt and vinegar flavour you can't go wrong !
As a fun exercise compare the aroma of unsalted and salted vinegars, that will tell you is your are getting an effect.
Peter
Hi Peter,
Salt 'n' vinegar does happen to be my preffered chrisp choice!
I will certainly compare both the salted and unsalted wood vinegars.
Cheers,
Joe
Salt and vinegar flavoured wood chips - love it - made me smile
As usual you have had some good suggestions - I particularly like the 2 for one effect from neutralisation of the acetic acid.
Since it is just out of curiosity and working with what you have why not try for a start
Headspace sampling for 1 min at ambient temp of
a) 1ml sample
b) 1 ml sample + 300mg of salt
c) 1ml of sample after neutralisation with sodium carbonate or bicarbonate
d) 1 ml water + the amount of sodium carbonate required in c) above as a blank in case it contains adsorbed volatiles
Don't spend too much time on it - you are looking at volatiles in a wide range of concentrations.
It will be an interesting learning curve for you
From experience the volatiles at a lower concentration may require 5 mins sampling at 65°C to capture and identify
Ralph
rb6banjo made some good points.
I think that I covered those off in my previous post - hope so anyway
I forgot to add blanks of
1ml water
1ml water + 300mg salt
Sometimes I found it beneficial to run a vial blank between each sample injection to ensure that the fibre was fully desorbed and that there was no carryover. And/Or using a splitless injection time of 1 minute before venting, leave the fibre in the injection port for another 4 minutes before removal to thoroughly clean it - does that make sense?
Ralph
Hi Ralph,
Thanks for the sample suggestions, I think I will have time to run these tomorrow in between my other jobs.
Your fibre cleaning method makes perfect sense! I already do something very similar as I desorb the fibre in the injection port for 5 minutes, but after 1 minute it purges to the split vent.
What sort of GC conditions should I be using for this? (oven temp, injection port temp, temp ramp, etc)
Cheers,
Joe
Know that the addition of the carbonate salt will titrate all of the acidic species (carboxylic acids, phenols, maybe thiols, etc.) in the solution so you likely won't see them anymore. Some things may also react at high pH - ester hydrolysis for instance. My philosophy on this sort of thing is do as little "harm" to the sample as possible until you realize that conventional means are not going to get you where you want to go. I would analyze the wood vinegar straight at first and then see what I get. If you find that the acidic species are of little interest, then add the carbonate salt to go after the neutral species and the basic species. A salt like sodium chloride is the best way to create high ionic strength yet not change the reactivity of the medium a great deal.
Hi rb6banjo,
I agree with your philosophy of doing no harm, so will progress using Ralph's suggestion above.
Cheers,
Joe