In olfactometry, one is constantly fighting to produce temporally precise and stable concentration outputs. This is especially critical when you want to make detailed measurements of perception or neural activity. Unfortunately, investigators are constantly confounded by artifacts that can distort the temporal properties and concentration profile of odor output. On this blog, I hope to eventually cover several issues that typically come up in calibrating olfactometers. In this first installment, I will deal with the issue of tubing after the jump.
There is general wisdom in the field that Teflon(R) tubing is the best choice of flexible tubing for olfactometry as it is least permeable to odors. However, this tubing is rather incompatible with pinch-valve based olfactometers. Here I will show how tubing choice influences odor output in a very simple system.
The setup is as follows:
The PID output from clean air being run through each type of tubing indicates how much odor is retained in the tubing and the decay in PID output indicates how fast the odor desorbes from the tubing. The PID output is measured in Volts. Output from a 100% AA bottle with Teflon tubing gives roughly 25 Volts.
These results are easier to see in bar graph form:
So, as expected Teflon is the best, but polyethylene is pretty similar to Teflon. Moral of the story: if you want to deliver odor, keep the amount of non-teflon tubing to a minimum!
PS. C-Flex tubing is such an odor sponge that passing odor through it actually reduces concentration at the output. Further, sorption/absorption and release are not symmetric at all! Here is what happens when you run through four 5sec odor pulses through C-flex tubing and then run through four clean air pulses:
There is general wisdom in the field that Teflon(R) tubing is the best choice of flexible tubing for olfactometry as it is least permeable to odors. However, this tubing is rather incompatible with pinch-valve based olfactometers. Here I will show how tubing choice influences odor output in a very simple system.
The setup is as follows:
- Two output channels: one clean & one "dirty"
- Flow to the PID switched between the two channels by pinch valves
- Tubing is made dirty by running 30 sec of Amyl Acetate through it @ > 350 ml/min
- The dirty tubing is then placed into the path of the PID and clean air was flushed through.
The PID output from clean air being run through each type of tubing indicates how much odor is retained in the tubing and the decay in PID output indicates how fast the odor desorbes from the tubing. The PID output is measured in Volts. Output from a 100% AA bottle with Teflon tubing gives roughly 25 Volts.
These results are easier to see in bar graph form:
Average amount of odor (Volts) retained by tubing. For reference, 100% AA vapor reads 25 Volts. |
Rate of odor release from tubing. |
PS. C-Flex tubing is such an odor sponge that passing odor through it actually reduces concentration at the output. Further, sorption/absorption and release are not symmetric at all! Here is what happens when you run through four 5sec odor pulses through C-flex tubing and then run through four clean air pulses:
Wonderful blog you have here but I was wondering if you knew of any forums that cover the same topics talked about in this article? I'd really love to be a part of group where I can get feed-back from other knowledgeable people that share the same interest. If you have any recommendations, please let me know. Bless you!
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