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This is, really, getting old. Couple weeks ago I was in the middle of a simple project, gluing together a handrail for the front stoup. I was congratulating myself for the beautiful, shiny mild steel beads on the filets, as the gas was decreasing in the tank. Then, the tank was just a few pounds from empty, so I called the LWS. Told me a fresh Q tank would be in on Friday. Called LWS on Friday to make sure they had fresh bottle before driving 25 miles to pick it up. No bottles. Clerk said he had a stubby of Argon, so I drove to pick it up.
Hooked up when I got home and went back to railing project. Gas inclusion in beads, so I switched to aluminum. Hard to establish bead, carbon contamination, little to no etching along beads. When I attempt to introduce rod into the puddle the end of the rod, immediately, balls up, inside a glob of crud. Just junk. 2,000 psi, running at 10 to 20 CFH at torch. Only difference in setup was new bottle. I've had several bottles with bad gas, but it didn't show up until pressure got to about 500 psi. Does anyone have tips on a sure-fire way to test jugs for gas quality? Last edited by Gadgeteer; 04-22-2022 at 08:56 PM. |
#2
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I'm confused. From steel to aluminum without changing anything but the bottle and filler mat'l?
__________________
Bill in sunny Tucson I believe in gun control. Gun Control: The ability to consistently hit what you are aiming at. Weldor by choice, engineer by necessity. |
#3
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After running old bottle down... I unhooked it... leaving gauges, hose, torch as was. When I got home with new "stubby" I hooked up the untampered gauge, hose, torch that were just the same, as I had left them. So, the only thing that was different in the setup was the new bottle of gas. But, after changing only the bottle, the beads on steel were showing signs of inclusion of something (gas?) that ruined the beads, not at all like the ones I had achieved with the old bottle of Argon. To further test for bad gas I switched over to aluminum by throwing the conversion switch on the machine from steel to aluminum. Didn't think I'd have to draw a picture to help you understand my methods. |
#4
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__________________
Bill in sunny Tucson I believe in gun control. Gun Control: The ability to consistently hit what you are aiming at. Weldor by choice, engineer by necessity. |
#5
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Same Tungsten, what tungsten are you using? Did you switch from DCEN on steel to AC on aluminum? What is your power source, air cooled or water cooled torch? What does your tungsten look like? Rarely are gasses bad, it is just a common excuse for other problems, when you do have a bad cylinder, it is often water in the cylinder from hydrotesting the cylinder. If the cylinder has been recently hydrotested you will see a recent date stamp on the neck of the cylinder, they often get repainted at the same time. The other problem is sometimes they guys might refill a gas mixture like 90/10 into what is supposed to be pure Ar. Or something similar, this I have heard of but again rare. I use actual flow meters on my cylinders vs. gauges. Most of the cheaper regulators use a high pressure gauge and a low pressure gauge that has been calibrated for flow rate, based on flow through an orifice. The problem is if you have a restriction in your torch you can show higher flow (in reality pressure) but not have that actual flow at the torch. If you are using an water cooled torch, you could have a small lead in your torch head. I have a few times tore my torch down cleaned it really good, reground my tungsten, made sure I had good laminar flow, etc. and without seeing any obvious issues the problem was solved. From what you have said, they 2 most likely issues you are dealing with would be: 1. a contaminated tungsten, break off the end and regrind, especially if you are switching back and forth between steel and aluminum. 2. shielding gas restriction between your supply and your torch.
__________________
Shade "Prepare to defend yourselves." -- Sergeant Major Basil L. Plumley, Ia Drang Valley |
#6
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I was too, but seeing the OP' 'tude, I'm not wasting any more time trying to finger out what they are trying to explain, nor provide some help.... ![]() |
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Adding to what the others have said above:
You should have indicated you were using TIG, some were thinking MIG. That you mentioned using same gas for Al and Fe was the tip-off it was GTAW. Knowing what your rig is would help. Power supply, torch, tungsten and size, etc. Before I start an arc, I will tap the pedal to initiate gas flow and purge the line. I instinctively listen for the "hiss" of gas out of the torch. Lack of hiss will remind me I didn't turn the gas on. ![]() You pics look like you are running out of gas and/or torch is getting hot.
__________________
TA Arcmaster 185 w/tig/stick kit MillerMatic 252 w/3rd gen 30A MM140 w/o AS, w/CO2 Hobart (Miller) 625 plasma Hobart 250ci plasma Victor O/A (always ready, but bored) HF 80 lunchbox w/tig 45ACP Black Talons for those stubborn jobs... |
#8
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contamination). External air movement contamination, aka fan or breeze; turbulent gas flow; or gas restriction in the lines or torch after the regulator.
__________________
Shade "Prepare to defend yourselves." -- Sergeant Major Basil L. Plumley, Ia Drang Valley |
#9
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I worked at a welding supply for 10 years,granted i worked on trucks and equipment but i did walk through the filling room almost daily.
we hydrostated our own cylinders but i don't remember water being put into the cylinder,the cylinder was dropped into a "well'' in the floor which was filled with water and sealed (like a pressure cooker) and then the cylinder was pumped up with i assume nitrogen. if the cylinder expanded it would displace the water in the well and up a pipe to a gauge with needle thing,it was an old machine and possibly the newer machines fill the cylinder with water? I worked for Strate welding,an airco dist. They had 3 men in the filling room and it would be hard to screw up a fill. Remember,the same filling rooms are filling Oxegen for medical and breathing air for air fed welding masks and paint shops. One welding gas that was i think a tri mix had to be rolled after filling,to mix the gas. It may have been a helium-argon-?something mix? They filled and then laid the cylinder on its side in a roller thing that gently rolled the cylinder,i guess for a certain amount of time? I quit there in 1990,so its been a few years. That tri mix could get screwed up if the cylinder was not rotated i guess,but your using straight argon? |
#10
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<Hooked up when I got home and went back to railing project. Gas inclusion in beads, so I switched to aluminum. Hard to establish bead, carbon contamination, little to no etching along beads. When I attempt to introduce rod into the puddle the end of the rod, immediately, balls up, inside a glob of crud. Just junk. 2,000 psi, running at 10 to 20 CFH at torch. Only difference in setup was new bottle. I've had several bottles with bad gas, but it didn't show up until pressure got to about 500 psi. Does anyone have tips on a sure-fire way to test jugs for gas quality?> Perhaps, when I wrote, "...that I was introducing rod into the puddle," it might have given you a clue that I was using tig. ![]() Last edited by Gadgeteer; 05-07-2022 at 02:33 AM. |
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