@ncpatch If a liquid is viscous that implies that the liquid has resistance to flow. For example petroleum gel and water, which is more viscous? The answer is petroleum gel as it flows more slowly than water across a slanted plane.
hii friends can any one give me information on what compounds can be dervitized??? and what is the exact method for sample extraction with the use of derivatizing reagents?? lidocaine, procaine mesalamine bupivacaine topermate can any of these be dervatized??
@shaggyburns you need to use the external, internal standard or standard addition method of anlysis to determine which peak is which if you have unknowns.
@shaggyburns One method I used is called preparative gc. A larger column and a larger volume of injectate is used. As the carrier gas exits the machine, dry ice cooled traps are inserted in the gas stream. Any liquids are thus trapped. Change the trap for each peak on the chromatogram, to isolate each compound. They can then be identified by standard methods, ie IR, NMR, Mass Spec, etc. Another method is to use a GC/Mass Spectrometer. High resolution MS will usually give a unique structure.
I didn't think you had to use the detector? Isn't it destructive? The GCMS does not have a detector because it is the ms aspect does that job??? is the gcms form of testing destructive?
GC detects relative amounts of some analyte. To find concentrations, usually you do the method of internal standards. You compare the area ratio between what you want as an analyte and some standard which has a fixed concentration of your choice. You make standards of your analyte (using known amounts of the analyte) with the standard to make a calibration curve. From the curve and running your unknown, you can find concentration.
Thank you so much ...... I'll be giving a lecture on Gas chromatography in 12 hrs ... I'll be showing this video via internet thanks a million RSC !!!!
since GC heats up the anlyte or specimen before the measurement or identification thus most organic substances like protein could not be evaluated or tested accurately or am I wrong please advice
the sample is heated quickly after it is injected into the injection port where it is vaporized then carried to the (nonpolar or polar) column.(Preferably, nonpolar column are used to prevent bleeding) This also regards the polarity of the sample and the column wall. Organic or inorganic samples can be tested. In this case protein, it must be homogenized into liquid form before using GC. Other parameters also play a factor in the identification of analytes in the sample
polarity has more to do with hplc, gc is the simple version og heating ur small liquid sample and breaking down the constituents of ur mixture for u to idenify through retention times and area peaks
factors which will affect the retention time of the compounds are;
volatility
polarity
column temperature
column packing polarity
flow rate of the carrier gas
length of the column
Volatility will generally be the main factor influence the separation. Polarity is only important if the mixture of compounds has compounds with widely different polarities.
i got a question here. so GC has nothing to do with the polarity of the substances used in order to separate them (because my teacher keeps on saying the polarity plays an important roll, like the more polar particles remain behind while the rest goes through the tube) ? because here and on other videos i here people mention only volatility of the substances as an important factor. :S :-? need explanation asap help help :p:p its for a project and great vid btw ;)
actually its more dependent on the volatility of the substances in your mixture. The more volatile compound in your mixture will be eluted (driven off) first followed by the less volatile, then lastly the least volatile one. Therefore you must know the boiling point of the substances in your mixture.
There are about 6 factors which will influence the retention time of the compounds in GC;
Volatility of the compound
Polarity
Column temperature
Column packing polarity
flow rate of the carrier gas
and length of the column
Volatility will have the greatest influence on the separation. Polarity is only important if you are separating compounds with widely different polarities.
polarity has more to do with liquid chromatography compared to gc, you familiar with the saying 'like dissolves like' and so on, gc just heats ur liquid sample, and breaks it down for a chemist to identify constituents of a mixture through their retention times and areas.
Well polarity indeed plays an important role as it defines the extent to which a given sample molecule interacts with the given GC column. There are specific columns depending on the type of sample molecules you need to analyse. I hope this helps :)
yes in GC the separation of analyte depends on its volatility but we should keep in mind that more polar the compound less volatile it would be,second thing the polarity of column in GC is also very important bcz inside the column the analyte molecules do not travle in a very straight line they move randomly and when they come in contact with the walls of coulmn they stay there for a while depending upon the polarity of analyte and column.
@traxass000 The components are sticking and being released LOTS of times. That stickiness has to do with the polarity of the column, and the polarity of the sample. Volatility is ease of evaporation. The particles are sticking to the coating on the stationary phase, coming off, and sticking again. Like dissolves like, so a polar chemical will stick and release to a polar column more times, thus coming off the column slower.
Hello. I want to ask about GC TCD-thermal conductivity detector can u show a video about it?
callmehoo 3 months ago
Any one know what viscous means?
ncpatch 3 months ago
@ncpatch If a liquid is viscous that implies that the liquid has resistance to flow. For example petroleum gel and water, which is more viscous? The answer is petroleum gel as it flows more slowly than water across a slanted plane.
callmehoo 3 months ago
hii friends can any one give me information on what compounds can be dervitized??? and what is the exact method for sample extraction with the use of derivatizing reagents?? lidocaine, procaine mesalamine bupivacaine topermate can any of these be dervatized??
bonny247 6 months ago
very nice. Thanks
crudeoilsystems 6 months ago
thanks
hplcflowmeter 6 months ago
how do you know which compound each peak is?
shaggyburns 9 months ago
@shaggyburns you need to use the external, internal standard or standard addition method of anlysis to determine which peak is which if you have unknowns.
shortie177 9 months ago
@shaggyburns One method I used is called preparative gc. A larger column and a larger volume of injectate is used. As the carrier gas exits the machine, dry ice cooled traps are inserted in the gas stream. Any liquids are thus trapped. Change the trap for each peak on the chromatogram, to isolate each compound. They can then be identified by standard methods, ie IR, NMR, Mass Spec, etc. Another method is to use a GC/Mass Spectrometer. High resolution MS will usually give a unique structure.
BuickDoc 2 months ago
Awesome! :D
asteriscotriangulado 10 months ago
I didn't think you had to use the detector? Isn't it destructive? The GCMS does not have a detector because it is the ms aspect does that job??? is the gcms form of testing destructive?
angelzpoo 10 months ago
I didn't think you had to use the detector? Isn't it destructive?
angelzpoo 10 months ago
Hello,
Does the GC detects a concentration or a number of mole?
I hope my question is clear enough to understand
Jerby7 1 year ago
@Jerby7
GC detects relative amounts of some analyte. To find concentrations, usually you do the method of internal standards. You compare the area ratio between what you want as an analyte and some standard which has a fixed concentration of your choice. You make standards of your analyte (using known amounts of the analyte) with the standard to make a calibration curve. From the curve and running your unknown, you can find concentration.
That's probably more than what you wanted lol.
analychemist 1 year ago
thanks for sharing!
Jerby7 1 year ago
thank you very much.
goalone09 1 year ago
Very informative and easy to understand! Thank you!
Sarimperil 1 year ago
very helpful video
farahfd20 1 year ago
thank u very much.
vamsipalaka 1 year ago
thanks
Ezequiel9425 1 year ago
Awesome... this is a great resource for preparing for organic lab
naturalfeatures 1 year ago
Thanks!
Thijswvv 1 year ago
Is it possible to see the ratio of CH3OH and C2H5OH in water with this method?
GingleGangle1 1 year ago
Is it possible to see the ratio of CH3OH and C2H5OH in water with this method?
GingleGangle1 1 year ago
I am building a gas chromatograph. I need some design parameters and a diagram for a Wheatstone bridge for my GC. Please help me.
Thank You
Zan
zzanzak 1 year ago
Thanks a lot for this video.
Puddy88 1 year ago
Thank you
forfuneee 2 years ago
this is very useful video.thanks for nice explaining
nanigad 2 years ago
Thank you so much ...... I'll be giving a lecture on Gas chromatography in 12 hrs ... I'll be showing this video via internet thanks a million RSC !!!!
rajeevvarma84 2 years ago
thanks alot for posting this video...i hope to get many informative videos in the future
suneetha4 2 years ago
thanks
AlgerienBiologist 2 years ago
since GC heats up the anlyte or specimen before the measurement or identification thus most organic substances like protein could not be evaluated or tested accurately or am I wrong please advice
darthsedious2000 2 years ago
@darthsedious2000
the sample is heated quickly after it is injected into the injection port where it is vaporized then carried to the (nonpolar or polar) column.(Preferably, nonpolar column are used to prevent bleeding) This also regards the polarity of the sample and the column wall. Organic or inorganic samples can be tested. In this case protein, it must be homogenized into liquid form before using GC. Other parameters also play a factor in the identification of analytes in the sample
nbo345 1 year ago
This video is excellent !
andoniashley 2 years ago
polarity has more to do with hplc, gc is the simple version og heating ur small liquid sample and breaking down the constituents of ur mixture for u to idenify through retention times and area peaks
pells09 2 years ago
To Traxass000
factors which will affect the retention time of the compounds are;
volatility
polarity
column temperature
column packing polarity
flow rate of the carrier gas
length of the column
Volatility will generally be the main factor influence the separation. Polarity is only important if the mixture of compounds has compounds with widely different polarities.
Good luck on your project
MrJason1234 2 years ago
Exelente ! ;gracias ,desde buenos aires.
bellinivernon 2 years ago
Really useful video :-) I'd be interested to see answer to traxass000 about precisely what is mean by volatility - does it refer to polarity?
thudu15 2 years ago
Thanks for the video... It help me alot! =D
markytproctor 2 years ago
interesting
sdoubaa 3 years ago
i got a question here. so GC has nothing to do with the polarity of the substances used in order to separate them (because my teacher keeps on saying the polarity plays an important roll, like the more polar particles remain behind while the rest goes through the tube) ? because here and on other videos i here people mention only volatility of the substances as an important factor. :S :-? need explanation asap help help :p:p its for a project and great vid btw ;)
traxass000 3 years ago 5
actually its more dependent on the volatility of the substances in your mixture. The more volatile compound in your mixture will be eluted (driven off) first followed by the less volatile, then lastly the least volatile one. Therefore you must know the boiling point of the substances in your mixture.
sparklingwine16 2 years ago
There are about 6 factors which will influence the retention time of the compounds in GC;
Volatility of the compound
Polarity
Column temperature
Column packing polarity
flow rate of the carrier gas
and length of the column
Volatility will have the greatest influence on the separation. Polarity is only important if you are separating compounds with widely different polarities.
Good luck on your project.
MrJason1234 2 years ago
polarity has more to do with liquid chromatography compared to gc, you familiar with the saying 'like dissolves like' and so on, gc just heats ur liquid sample, and breaks it down for a chemist to identify constituents of a mixture through their retention times and areas.
pells09 2 years ago
Well polarity indeed plays an important role as it defines the extent to which a given sample molecule interacts with the given GC column. There are specific columns depending on the type of sample molecules you need to analyse. I hope this helps :)
sam4phd 2 years ago
Hi,
yes in GC the separation of analyte depends on its volatility but we should keep in mind that more polar the compound less volatile it would be,second thing the polarity of column in GC is also very important bcz inside the column the analyte molecules do not travle in a very straight line they move randomly and when they come in contact with the walls of coulmn they stay there for a while depending upon the polarity of analyte and column.
shoukatkhan01 2 years ago 7
@traxass000 The components are sticking and being released LOTS of times. That stickiness has to do with the polarity of the column, and the polarity of the sample. Volatility is ease of evaporation. The particles are sticking to the coating on the stationary phase, coming off, and sticking again. Like dissolves like, so a polar chemical will stick and release to a polar column more times, thus coming off the column slower.
Yibitech 10 months ago
Very good. thanks
sweetprinci 3 years ago
Thanks, this was very useful!
Tescanna 3 years ago
thanks
chemistosama 3 years ago
thanks
chemistosama 3 years ago
thanks
chemistosama 3 years ago
thanks for posting this video. Very informative.
robecbecs 3 years ago
Thank you!
alexrs2k 3 years ago
Thanks for posting
macmenmen 3 years ago