J.R. S. answered 08/03/23
Ph.D. University Professor with 10+ years Tutoring Experience
Probably the easiest place to start is by looking at your table and finding the ppb for each internal standard (spike). The ppb will be equal to the mls used, i.e. 2.5 mls = 2.50 ppb final; 5.00 mls = 5.00 ppb final, etc.
0 ppb
2.50 ppb
5.00 ppb
7.50 ppb
10.00 pb
Next step is to construct a standard curve from the 0 ppb to 10.00 ppb added. So plot the ppb on the x-axis against the Absorbance values on the Y-axis. Either do a linear regression analysis or simply eye-ball the best straight line. If you have the linear regression line, plug in 0 for Y and solve for x, or divide the y-intercept by the slope. That will be the ppb in the sample used.
Then you will have to correct for dilution and aliquoting factors. If you can get to the point of obtaining the straight line and finding ppb from that graph, I'd be happy to work through the correction factors to get the answer in mg Cd2+ / g dry clam. But it's difficult to do without actual numbers.
If x = 4.9 ppb, then this was in a 5 ml sample from a 100 ml solution. Thus, the 100 ml solution is also 4.9 ppb. But this 100 ml solution came from diluting 5 mls of the original 100 mls extract. So that represents a 20-fold dilution. Thus, the original 100 ml (0.1L) extract has 20 x 4.9 ppb = 98 ppb. This is equal to 98 ug/L Cd2+.
So, total ug of Cd2+ in the original extract = 98 ug / L x 0.1 L = 9.8 ug Cd2+
This arises from 80.83 mg of clam tissue. Thus we have 9.8 ug Cd2+ / 80.83 mg tissue = 0.1212 ug / mg tissue
Converting this to mg Cd2+ / g clam tissue,
0.1212 ug Cd2+ = 1.21x10-4 mg Cd2+
1 mg tissue = 1x10-3 g tissue
[Cd2+] = 1.21x10-4 mg Cd2+ / 1x10-3 g tissue = 0.121 mg Cd2+ / g clam
Yash P.
Okay so I did a linear regression on desmos and then got y= 0.01612x + 0.08 and when plugging in y=0 I got -4.9 for x so how would I go from here?08/03/23