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- The same polar compound is gas chromatographed on an SE-30 (very nonpolar) column and then on a Carbowax 20M (very polar column). I low will K=cS/cM vary between the two columns?what can be an analyte for using internal standard? sample: vegetable oil containing ethyl oleate, IS: Ethyl oleate. what should be analyte here (what mixture composions) to use for internal standard method and calibration?The detecton limits reported for Al with ICP-AES and GF-AAS are 2 ppb and 5 picograms, respectivly. If we assume that a 20 microliter sample volume is used for the GF-AAS determination, which method has the lower detection limit? (1 picogram = 10-12 gram.)
- What is the role of stationary phase and mobile phase in Chromatography? Please shortly answer at your own words. Answer should be to the point (specific 4-5 lines).A 0.0200 gram blood sample was decomposed by a microwave digestion technique followed by dilution to 100.0 mL in a volumetric flask. Aliquots of the sample solution were treated with a lead complexing reagent and water as follows: Solution 1: 10.0 ml blood sample + 20.0 mL complexing agent + 30.0 mL H20. Solution 2: 10.0 ml blood sample + 20.0 mL complexing agent + 26.0 mL H20 + 4.00 mL of 78 ppb Pb2+ standard. The resulting solutions were analyzed by UV/Vis at 375 nm. Absorbance for solution 1 = 0.155 and for solution 2 = 0.216. Calculate the concentration of lead (ppb) in the original sample.1 mL was taken from the sample filtrate and mixed with 13 mL pure water and 4 mL sulfomolybdic acid and 2 mL dilute SnCI2 solution by adding it, and after waiting for 15 minutes, the absorbance of the resulting solutions against pure water was read at 520 nm. if the function of the calibration graph obtained with standard phosphorus solutions of 0.5-2.5 mg/mL is y= 0.245x + 0.107 and the absorbance of the serum sample is 0.342, how many grams of phosphorus is the amount in the sample?
- An analyst determines the Cl^- content of rain water with ion chromatography. The data for the calibration line in the range 5 to 50 milli equivalents per liter (mEq/L) is shown in the table below. Additionally, a blank sample was analysed 5 times and the following results obtained: 1.1, 0.5, 0.1, 0.9 and 1.2 ppm Ct Calculate the detection limit (DL) for the method with a 98.3% confidence level. Use ALL data and show equationsFT-IR technique can be utilized for the analysis of unknown analytes by matching it with__________. Both choices are correct Commercial library/database Reference standardConsider a separation performed on a 35.0 mm long open tubular colum with a 0.500 mm diameter and a 2.0 ? m thick stationary phase. Compound A eluted at 12.63 min and compund B eluted at 13.30 min. A compund known not to be retained at all by the stationary phase eluted at 1.145 min. Calculate the relative retention.
- The same chloride analysis but using a new method for which the standard deviation was not known, gave the following replicate results, mean and estimated standard deviation: Chloride (ppm) = 346, 359, 350; Mean = 351.67 ppm; Standard deviation = 6.66ppm. Solve for the CI for the 3 determinations at 95% probability level.You are developing a procedure for determining traces of copper in biological materials using a wet digestion followed by measurements by atomic absorption spectrophotometry. In order to test the validity of the method, you obtain a NIST orchard leaves standard reference material and analyze this material with your procedure five times and obtain a mean of 12.27 ppm with a standard deviation of 0.097 ppm. The NIST sample is listed as 11.7 ppm. Does your method give a statistically valid value at the 95% confidence level?In a High Performance Liquid Chromatography (HPLC) analysis, toluene exhibits a capacityfactor of 3.5 on a 15.0 cm column. The unretained solute is eluted at 1.33 min (tm). a) Determine the retention time tR of toluene. b) Calculate the number of theoretical plates and the plate height that would produceatoluene peak eluting at 12.83 min with a width at the base of 18.4 s