Update, I got peaks by ~doubling the tubing length from my Rx coil to the detector. Peak looks Gaussian but small.
I am using the 547 buffer recipe of 19.1g borate, 100 mg OPA, and 100 ul of 1:1 ACN/ mercaptol ethanol.
I am following a paper from Waters who's recipe is 19.1 g borate, 800mg OPA and 2 ml mercapto ethanol (no idea if it is a 1:1 mix with ACN).
I'll try the Waters recipe tomorrow.
I used that Waters mixture about 20 years ago when I had the Waters equipment. It will work but the excessive OPA and mercaptoethanol will stain all of your tubing dark blue and you will need to wash the cell often with straight Acetone to keep it clean.
I switched to the Hamilton PRP X400 column from the Waters column and never had any problems. We tried the Pickering column and while it worked great, it was not compatible at all with Methanol, and if you didn't get the Methanol washed out after doing Carbamates you would ruin a $1500 column.
Look up the Hamilton procedure and they have trouble shooting ideas which say that if you have AMPA but no Glyphosate you need more bleach. Too much bleach and you will begin to lose both, so it is a balancing act. Also if the reactor is too hot, you will not get peaks, 36C is what we use.