I was just looking back through your thread to see what pressures you were running at and came across this.
I thought the same thing as you at first, but I changed my mind after using it for a while. I thought it wasnt staying calibrated at first, but it was always close enough when I checked it - meaning the IN and OUT were always within a few points of each other. Maybe 2% difference between them at most.
Then I read that the calibration needs adjusting if there is no flow or really low flow rates. However, there is only a very small change at the flow rates Im running at.
For example, right now my system is running at .7 seconds ON and 50 seconds OFF which is about .7 gallons per day flow rate. The meter is reading 336 on the IN and 348 on the out. Both fluctuate a point or two every so often - but not exactly when the nozzles fire.
When I change the cycle to .7 sec ON and 2 seconds OFF or 25 times the flow rate = closer to 17 gallons per day, the IN reading drops from 336 to 335, and the OUT reading drops down from 348 to 344/345. So not a big change at all. Its actually not much more variation than what I see when there is no flow at all.
I dont really care what the exact, or absolute value of the readings from the HM are anyway. I get that reading from the rez using my BlueLab meter. The HM meter is more to track the ādifferenceā between the in and out rather than the actual TDS value. It seems to be good for doing that.
I monitor the rez when Im making changes to the nute concentration, but pay attention to the difference between IN/OUT to check how the roots are feeding and if I need to raise or lower the EC in the rez.
So far - with almost no roots in the system - that difference of 8 to 12 points is holding pretty constant. The only time it changes is when I forget to turn the heater for the root chamber back on after I have been working on the chamber.
I have the root chamber heater set to keep it between 68 F and 70F. When the root chamber is cooled down to 65 F or below, there is less difference between the IN/OUT readings. Im sure whats happening is the droplets evaporate to some degree while they are suspended. A warmer root chamber makes for faster evaporation. That in turn increases the concentration of nutes left in the droplets that collect in the bottom of the rez and raises the TDS reading on the OUT probe.
Once the roots get bigger, I should be able to tell how they are feeding by watching to see if that IN/OUT difference goes up or down. I hope