3.2/8 = 0.4......do check it....
Differential spectrophotometry is a spectrophotometric analytical technique in which a solution of the sample's major component is placed in the reference cell and the recorded spectrum represents the difference between the sample cell and the reference cell...basically it uses major component of system as reference and NOT solvent ..for example if a enzyme ligand system is to be assayed ..enzyme + solvent is reference and enzyme + ligand + solvent is test sample..its for quantitative detection.
If the original spots were below the level of developing solvent then the components of the spotted sample would dissolve into the solvent and no spots would be seen upon analysis because all of the sample is dissolved in the developing solvent. hope this helps. good luck in o. chem!
You may not need to treat it at all. First step is to take a sample to get analysed at a lab and find out how pure it is.
The advantages are: - Goldfish requires less solvent than Soxhlet (solvent in Soxhlet has to reach the siphon level). - Goldfish is quicker because the sample is constantly in contact with the solvent. Source: CECCHI, Heloísa Máscia."Fundamentos Teóricos e Práticos em Análise de Alimentos". Editora Unicamp. 2a Edição. 207p. 2003.
It is the distance travelled by the sample or analyte divided by distance travelled by the solvent front in chromatography.
Differential spectrophotometry is a spectrophotometric analytical technique in which a solution of the sample's major component is placed in the reference cell and the recorded spectrum represents the difference between the sample cell and the reference cell...basically it uses major component of system as reference and NOT solvent ..for example if a enzyme ligand system is to be assayed ..enzyme + solvent is reference and enzyme + ligand + solvent is test sample..its for quantitative detection.
No you can't. what an idiot
You have a sample analysed then use the appropriate filters.
Take a sample to a lab to get analysed.
Only way to find out - is to take a stool sample to a vet and have it analysed.
Get a sample analysed at a lab FIRST -so you know what to do .
This is 'turbidity' and is measured in 'ppm' when you have a water sample analysed in a lab.
You call a well or filtration company . First get a sample analysed at a lab.
the light from the lamp below the table would not get through the sample, meaning it could not be seen or analysed.
You get a sample analysed then use appropriate filters for whatever is making it brown.
take a genetic test - a blood or tissue sample is analysed for specific mutations
You may need an Iron filter. -Take a sample to be analysed at a lab.