What r the limitatoins of uv visible spectroscopy ? Why
Water use in blank standard for uv visible spectroscopy ?
Answers were Sorted based on User's Feedback
Answer / tanu bhardwaj
when we prepare a solution for UV-vis spectroscopy, we prepare it in a solvent, to remove the absorption effects due to solvent, we keep that solvent into blank, so that when the two rays coming out of two cuvettes are subtracted, then we get only the absorption due to solute, not due to solvent. if we prepare sample in water, then water is used as blank.
| Is This Answer Correct ? | 39 Yes | 2 No |
Answer / pnreddy
uv 200nm to 400nm
visible 400nm to 800 nm
because solvent is water
| Is This Answer Correct ? | 34 Yes | 29 No |
Answer / naveen kumar
UV is not applicable for the high concentration solutions means 0.01M Nd it is not applicable for suspensions emulsions coagulated products Nd florescence substances
| Is This Answer Correct ? | 3 Yes | 0 No |
Answer / kamil hassan
limitation of uv visible spectrometer from 200 nm to 800 nm range. 200 to 400nm uv wavelength & 400 to 800 in visible Wavelength '
water we used as a solver in spectrometer because its absorb on only 165 nm (vacuum uv range) so why we used deionized water as a Blank.
| Is This Answer Correct ? | 4 Yes | 5 No |
What is linearity in hplc and how to calibration
What is difference between Chromatographic purity and Related substances analysis?
What are the different zones in stability according to ICH?
UV and PDA detector, which have less signal to noise ratio?
What is pooled sample in Dissolution
2 Answers Graviti Pharmaceuticals, Lupin,
what is the principle involved in turbidometry and nephelometry ?
0 Answers Graviti Pharmaceuticals,
define beer-lambertslaw.
is a bonded water molecule in an organic material can be easlisy and accuractly determined by KF rather than LOD
i set electrode to 7 buffer than i used it to check 4 buffer and 10 buffer if the results are not as expected than is it better to set the buffer again to 4 buffer or is there any other method available please let me know ...
I have compare C2H2-air and C2H2-N2O flame AAS on determination calcium. Both use same range of std to plot calibration curve. (2-6ppm) When i measure the sample with phosphate, KCl and LaCl, C2H2-N2O flame give false positive result, around 0.5ppm. When i measure the sample with phosphste, KCl and EDTA. C2H2-N2O flame also give 0.5ppm false positive. But both above mentioned sample would not give false positive when measured by C2H2-air flame. What is the reason?
what is the difference between c-8 and c-18 column
What are the terms used during Melting Range Analysis ?