Substances A and B have retention times of 16.40 and 17.63 minutes, respectively, on a 30.0...
- Substances A and B have retention times of 16.40 and 17.63 minutes, respectively, on a 30.0 cm column. An unretrained species passes through the column in 1.30 min. The peak widths at the base for A and B are 1.11 and 1.21 minutes, respectively. Calculate a) column resolution, b) average number of plates in the column, c) plate height.
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Substances A and B have retention times of 16.40 and 17.63
minutes, respectively, on a 30.0...
1. Listed below are retention times and peak widths for an HPLC chromatographic separation on a...
1. Listed below are retention times and peak widths for an HPLC chromatographic separation on a 10 cm C18 column a) Calculate the resolution between benzene and benzo[e]pyrene. Compound Unretained Benzene Benzo[e]pyrene Pyrene Coronene Time (min) Baseline Width (min) 0.9 10.9 13.3 16.7 26.1 0.40 0.40 0.45 0.50 b) Is this a good resolution, yes, no, why? c) Calculate the theoretical number of plates for benzo[elpyrene.
A student researcher performed a chromatographic separation of caffeine and aspartame. The retention time for caffeine,...
A student researcher performed a chromatographic separation of caffeine and aspartame. The retention time for caffeine, is, was found to be 218.0 s with a baseline peak width, wc, of 14.4 s. The retention time for aspartame, 1., was 250.5 s with a baseline peak width, w of 21.1 s. The retention time for the unretained solvent methanol was 40.4 s. Calculate the average plate height, H, in micrometers for this separation, given that it was performed on a 27.7...
Two compounds C and D are separated on a column 34 cm long . Given the...
Two compounds C and D are separated on a column 34 cm long . Given the chromatographic data below calculate The column resolution? , the number of theoretical plates ?the height of theoretical plate and what length of column would be required to give a resolution of 1.5? Compound C retention time 18.3 width at base of peak(min) = 2.18 Compound D retention time 17.7, width at base 1.23
3. a) b) c) How many theoretical plates produce a chromatography peak eluting at 4.78 min...
3. a) b) c) How many theoretical plates produce a chromatography peak eluting at 4.78 min with a full width at half max (FWHM) of 1.20 s? The length of the column is 30.0 m. What is the plate height in microns? What is the peak resolution for this peak and another peak eluted at 4.73 minutes that has a full peak width (measured at the base) of 2.14 seconds? Is this sufficient for quantitative analysis of those two components?...
The table contains data for a liquid chromatography separation of four compounds, A, B, C, and...
The table contains data for a liquid chromatography separation of four compounds, A, B, C, and D, on a 40.0 cm column Retention Compound time (min) Width at the base (min) A 5.17 0.436 B 1.02 13.0 15.0 C 1.10 23.4 1.91 Calculate the number of theoretical plates, N, for each peak. NA NB Nc ND = What is the average number of theoretical plates, Navg, for Navg the column? What is the plate height, H, for the column? Н-...
EXERCISE 6: Two chemical species, A and B are separated by isothermal gas chromatography, using a...
EXERCISE 6: Two chemical species, A and B are separated by isothermal gas chromatography, using a 2.00 m column having 5000 theoretical plates at a flow rate of 15.0 ml / min. The peak of unabsorbed air appears after 30 s; the peak of A appears after 5 min and that of B after 12 min (a) Calculate the dead volume VM of the column, and the retention volumes Va and VB. (b) Calculate the reduced volumes V’a and V'B...
Consider a separation performed on a 45.0 mm long open tubular column with a 0.50 mm...
Consider a separation performed on a 45.0 mm long open tubular column with a 0.50 mm diameter, and a 2.0 um thick stationary phase. Compound A eluted at 12.41 min, compound B eluted at 13.34 min, and the unretained solvent eluted at 1.130 min. What are the adjusted retention times, t, and retention factors, k, for compounds A and B? Number Number min Number Number min rB What is the relative retention, a, for this separation? Number roll down to...
Two isotopic compounds are produced in the synthesis of a new therapeutic drug, which must be...
Two isotopic compounds are produced in the synthesis of a new therapeutic drug, which must be separated by repeated chromatography cycles. In each cycle, the solution containing both compounds passes through a chromatography column of length ?=45.0 cm containing ? theoretical plates. The compounds have an adjusted relative retention, α, of 1.093 and retention factors of 6.09 and 6.66 , respectively. Calculate the number of theoretical plates, ? , in the column of length ? . The observed resolution is...
A group of analysts was working on developing a method to separate and determine carbamate insecticides...
A group of analysts was working on developing a method to separate and determine carbamate insecticides used for control of pests in food production They used HPLC with an Eurospher 100-5 C-18 column and a mobile phase consisting of a mixture of water and methanol, with post-column derivatization. .The column was determined to have an average of 1999 theoretical plates for this group of compounds. The stationary and mobile phases volumes in the column were SMV = 0.51mL, V =...
Length of column = 30.50 cm Flow rate = 0.313 mL/min A chromatogram of a mixture...
Length of column = 30.50 cm Flow rate = 0.313 mL/min A chromatogram of a mixture of species A, B, C, and D provided the following data: Species Retention time, minutes Width of peak base (W), minutes A 5.4 0.41 B 13.3 1.07 C 14.1 1.16 D 21.6 1.72 Calculate the resolution for species C and D
1. Listed below are retention times and peak widths for an HPLC chromatographic separation on a 10 cm C18 column a) Calculate the resolution between benzene and benzo[e]pyrene. Compound Unretained Benzene Benzo[e]pyrene Pyrene Coronene Time (min) Baseline Width (min) 0.9 10.9 13.3 16.7 26.1 0.40 0.40 0.45 0.50 b) Is this a good resolution, yes, no, why? c) Calculate the theoretical number of plates for benzo[elpyrene.
A student researcher performed a chromatographic separation of caffeine and aspartame. The retention time for caffeine, is, was found to be 218.0 s with a baseline peak width, wc, of 14.4 s. The retention time for aspartame, 1., was 250.5 s with a baseline peak width, w of 21.1 s. The retention time for the unretained solvent methanol was 40.4 s. Calculate the average plate height, H, in micrometers for this separation, given that it was performed on a 27.7...
3. a) b) c) How many theoretical plates produce a chromatography peak eluting at 4.78 min with a full width at half max (FWHM) of 1.20 s? The length of the column is 30.0 m. What is the plate height in microns? What is the peak resolution for this peak and another peak eluted at 4.73 minutes that has a full peak width (measured at the base) of 2.14 seconds? Is this sufficient for quantitative analysis of those two components?...
The table contains data for a liquid chromatography separation of four compounds, A, B, C, and D, on a 40.0 cm column Retention Compound time (min) Width at the base (min) A 5.17 0.436 B 1.02 13.0 15.0 C 1.10 23.4 1.91 Calculate the number of theoretical plates, N, for each peak. NA NB Nc ND = What is the average number of theoretical plates, Navg, for Navg the column? What is the plate height, H, for the column? Н-...
EXERCISE 6: Two chemical species, A and B are separated by isothermal gas chromatography, using a 2.00 m column having 5000 theoretical plates at a flow rate of 15.0 ml / min. The peak of unabsorbed air appears after 30 s; the peak of A appears after 5 min and that of B after 12 min (a) Calculate the dead volume VM of the column, and the retention volumes Va and VB. (b) Calculate the reduced volumes V’a and V'B...
Consider a separation performed on a 45.0 mm long open tubular column with a 0.50 mm diameter, and a 2.0 um thick stationary phase. Compound A eluted at 12.41 min, compound B eluted at 13.34 min, and the unretained solvent eluted at 1.130 min. What are the adjusted retention times, t, and retention factors, k, for compounds A and B? Number Number min Number Number min rB What is the relative retention, a, for this separation? Number roll down to...
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