I'm currently trying to study mercury conversion by bacteria using CV-AFS. I've tried some different containers ( tests without using bacteria) like glass (20ml capacity), PP (polypropilene) (10ml) and PVC containers (40ml). I usually use 15 or 6.3ml of muller hinton media (a rich medium, pH=7), and inject HgCl2 to work with a concentration between 800 and 1000ppb of mercury. The vessels are placed horizontally with an orbital agitation of 120rpm and at 37ÂșC.
I keep taking aliquots of 1ml at 0, 24 and 48H. The problem is the mercury levels keep falling after sample analysis, to a point that at 48 hours i only have between 30 to 50% in glass, and in polymer between 10-30%.
Can disproportionation of mercury account for these losses. I tried washing the vessels after the test with HNO3 and water (50:50) at 65% but i can only recover between 10 and 30% of mercury, therefore probably adsorbed.
Are the aliquots i take too much?
My teacher says i'm crazy, and that the error must be human (meaning, mine)., but i have already a lot of tests, that even though are not very reproductible corroborate a permanent loss of mercury. All these tests without bacteria.
Can anybody give me a hand here?!
(my teacher is freakin out! She states that she used those vessels to keep biological samples in the freezer, and that there was never a loss above 10% of mercury).