From the data please calculate:a) an average number of plates from the datab) the standard deviation for the average in a)c) an average plate height for the column 31-28. The following data were obtained by gas-liquid chro-matography on a 40-cm packed column:CompoundReAirMethylcyclohexaneMethylcyclohexeneToluenetr, min1.910.010.913.4W, min0.760.821.06Calculate(a) an average number of plates from the data.(b) the standard deviation for the average in (a).(c) an average plate height for the column.

Answered: Image /qna-images/answer/e553e3c5-c285-46b8-ba50-95e37580fc22.jpg

31-28. The following data were obtained by gas-liquid chro- matography on a 40-cm packed column: Compound Air Methylcyclohexane Methylcyclohexene Toluene tr, min 1.9 10.0 10.9 13.4 W, min — 0.76 0.82 1.06 Calculate (a) an average number of plates from the data. (b) the standard deviation for the average in (a). (c) an average plate height for the column.

31-28. The following data were obtained by gas-liquid chro- matography on a 40-cm packed column: Compound Air Methylcyclohexane Methylcyclohexene Toluene tr, min 1.9 10.0 10.9 13.4 W, min — 0.76 0.82 1.06 Calculate (a) an average number of plates from the data. (b) the standard deviation for the average in (a). (c) an average plate height for the column.

Principles of Instrumental Analysis

7th Edition

ISBN:9781305577213

Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch

Publisher:Douglas A. Skoog, F. James Holler, Stanley R. Crouch

Chapter26: An Introduction To Chromatographic Separations

Section: Chapter Questions

Problem 26.14QAP

See similar textbooks

Similar questions

A young researcher was evaluating a standard method for determining the methylmercury content in blue fin tuna using high performance liquid chromatography (HPLC). She determined the standard deviation (?)(s) for the method to be 0.440.44 ppb and assumed that ?s was a good approximation of ?σ . As a test, she used this method to evaluate the methylmercury content in a National Institutes of Standards and Technology (NIST) standard and determined the unknown amount to be within 0.210.21 ppb (?)(μ) of the known mean with 99% probability. How many replicate measurements of the NIST standard did the researcher perform?
For Indirect Iodometric Analysis of Copper... ~0.0896g KIO3 necessary to consume 350mL of 0.1 M Na2S2O3, Na2S2O3 is stored in an amber glass bottle until ready for use. Primary Standard KIO3 has 2g of KI, 50mL of DI water, and 10 mL of 1.0M HCl is added then immediately titrated with Na2S2O3 until medium yellow or straw... then 5mL of starch indicator is added and titrated again until blue black color turns clear. Unknown CuO use 1.2G of Unknown, 20mL of HNO3 heated until sample dissolved, 25 mL of DI water added and boiled until clear light blue color, after cooling 1:1 NH3 added (~34.47 mL of NH4OH reagent) until permanent deep blue color amine complex, 2g of NH4HF2 added and swirled until dissolved, 3 g of KI is added then titrated immediately with Na2S2O3 until brown color of iodide is nearly gone (brown milk color), 2 g of KSCN and 3 mL of starch indicator is then added with titration continuing until disappearance of new blue black color. 1. Na2CO3 is often added to thiosulfate…
For Indirect Iodometric Analysis of Copper... ~0.0896g KIO3 necessary to consume 350mL of 0.1 M Na2S2O3, Na2S2O3 is stored in an amber glass bottle until ready for use. Primary Standard KIO3 has 2g of KI, 50mL of DI water, and 10 mL of 1.0M HCl is added then immediately titrated with Na2S2O3 until medium yellow or straw... then 5mL of starch indicator is added and titrated again until blue black color turns clear. Unknown CuO use 1.2G of Unknown, 20mL of HNO3 heated until sample dissolved, 25 mL of DI water added and boiled until clear light blue color, after cooling 1:1 NH3 added (~34.47 mL of NH4OH reagent) until permanent deep blue color amine complex, 2g of NH4HF2 added and swirled until dissolved, 3 g of KI is added then titrated immediately with Na2S2O3 until brown color of iodide is nearly gone (brown milk color), 2 g of KSCN and 3 mL of starch indicator is then added with titration continuing until disappearance of new blue black color. 4. Why is the starch indicator solution…
In the determination of ethanol concentration in alcoholic beverages using the GCFID method, why do we need to calculate the coefficient variation (CV). standard deviation, repeatability, response factor and response ratio? And how to calculate this parameter?
The following results were obtained in the replicate determination of the lead content of a blood sample: 0.752, 0.756, 0.752, 0.751, and 0.760 ppm Pb. Calculate the relative standard deviation and coefficient of variation of this set of data
how much iron ore (that assays at 33.8% fe) must be used in an analytical procedure that is known to have a low bias of -0.15g if an overall relative error of 2.09 ppth in the iron content is desired
The following results were obtained for the determination of calcium in a NIST limestone sample: %CaO = 50.33, 50.22, 50.36, 50.21, and 50.44. Five gross samples were then obtained for a carload of limestone. The average %CaO values for the gross samples were found to be 49.53, 50.12, 49.60, 49.87, and 50.49. Calculate the relative standard deviation associated with the sampling step
You are developing a Ca detection method for a graphite furnace AA instrument. Your analysis of ten blank samples gives a standard deviation of 0.265 ppb. To establish your limit of detection (LOD), what concentration of Ca should be spiked into your blanks?
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.)
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.
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.
The concentration of purified OXA-M290 is tested with a BCA assay. Serial dilutions of a bovine serum albumin (BSA) stock solution are prepared, then pipetted into a 96-well plate; each dilution of the BSA standard is tested in triplicate. Then, bicinchoninic acid and Cu2+ ions are added to all of the wells of the plate. After incubating the plate for 1 hour, a microplate reader is used to measure the absorbance of all of the wells in the plate at 560 nm. This generates the following data: BSA conc. (μg/mL), Replicate 1 Absorbance, Replicate 2 Absorbance, Replicate 3 Absorbance 40, 1.360, 1.403, 1.481 20, 0.750, 0.745, 0.810 10, 0.380, 0.344, 0.398 5, 0.198, 0.160, 0.183 2.5, 0.090, 0.100, 0.085 1.25, 0.038, 0.043, 0.051 0.625, 0.024, 0.028, 0.019 Prepare a calibration curve using these data. You can use Excel, R, SPSS or an equivalent graphing software. In this graph, plot absorbance (y-axis) against the concentration of the protein standard (x-axis). Calculate and plot…