03-26-2008 11:04 AM
03-26-2008 09:11 PM
Hi esra,
When you change to linear scale, you see the autocorrelation as a triangle. That means the second half decays linearly, not exponentially. So you will not get a high decay rate when you perform exponential fit on it.
Michael
09-09-2008 01:08 PM
hi esra
I am trying out feasibility of setting up dynamic light scattering experiment. I would like to know about the kind of oscilloscope that you had used for the experiment. What was the bandwidth of the oscilloscope? how successful was your attempt and whats the range of particle size you could determine? please do enlighten me to proceed further with the experiment.
deepa
09-12-2008 09:26 AM
Hello deepa
I was using Lecroy 9304A oscilloscope. my particles were in range 20-100 nm. I saw signal with this particles designed the set up. but I could never get autocorrelation function work in labview. Let me know if you have any suggestions about doing autocorrelation using labview.
thanx
09-12-2008 10:54 AM
Hi esra, Thank you for your reply. I havent started with the set up but planning to do so soon. I will try doing autocorrelation in LabVIEW and will surely let you the know the outcome.
Deepa
12-10-2009 03:01 PM
esra
I am trying to do a similar experiment as you and I am running into the same problem. Did you every find a solution?
thanks
12-11-2009 03:40 PM
12-11-2009 06:49 PM
Hey Mike S.
I am using the autocorrelation VI in labview, however, the help screen is not very helpful for me. I know i need to modify the data some how, but i am not sure what steps i need to take in order to get the appropriate function. It should come out as a sigmoidal decay when the x axis is in the log scale and the y axis is linear, but i am getting a triangle. If you have any ideas please let me know.
Thanks
ay7973
12-14-2009 05:45 PM
12-18-2009 01:27 PM
To Mike S. and anyone else who knows anything about this:
Here is the whole story (the relevant part anyway). Currently I have the NI Diadem software, I am not sure if u are familiar with it, but it is a data analysis software. It includes an autocorrelation function. When I put identical data into the diadem autocorrelation function and the labview autocorrelation function VI I get different output curves. I have no idea why this is. I have attached the data i am using in an ASCII file and ii have also attached the two curves i am getting with the data in the respective programs.
In labiew, all I have done was connect a read file VI to the autocorrelation VI to a waveform indicator.
I need any help I can get at this point.