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#1
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![]() Quote:
The difference in clarity between the two vials is enough to throw your reading off.
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I have to go out and buy more snails for my hermit crabs. |
#2
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![]() if that's the case and we can't assume that two seemingly identical vials are the same to the meter then perhaps even inserting the same vial back into it but rotating it differently could be a factor too.
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#3
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![]() Bingo... Which is why the Hanna colorimeters for phosphate get such bad reviews. They are a pretty flawed method if two different vials, etc. interfere with the reliable results. And having an auto-off of three minutes when simply mixing the reagent takes a minimum of two was just poor planning...
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I have to go out and buy more snails for my hermit crabs. |
#5
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![]() Quote:
why else would they give us two lol? |
#6
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![]() Geez guys, it is really not that hard... I only use one vial, and always get it completely mixed every time. Like I said, just have to do it right as described above, and it is then very accurate and consistent.
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Reef Pilot's Undersea Oasis: http://www.canreef.com/vbulletin/sho...d.php?t=102101 Frags FS: http://www.canreef.com/vbulletin/sho...d.php?t=115022 Solutions are easy. The real difficulty lies in discovering the problem. |
#7
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![]() my readings sometimes vary so it's good conversation to me. if there's ways to make the process more accurate it's worth discussing.
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#8
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![]() Maybe I'm slow, but I cannot fill vial, add ALL the reagent in the pouch, and completely mix it in 3 min. At the end of 3 min I still have solid particles of reagent swirling in the vial. I don't want to measure it unless it's completely dissolved. That's why I use 2 vials.
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#9
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![]() when I started and was slow with the Hanna was using both vials. Now do the C1, add reagent, shake, hold the button to get the 3 minute timer started then done. Seen a video where you crease the packet to get a funnel helps to pour.
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my tank |