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- Briefly explain four importance of conducting sample preparation prior to instrumental analysis.
- Consider the following situations:
- If you were to analyse traces of petroleum from a piece of burned carpet, which sample preparation method is more suitable, solid phase microextraction (SPME) or pressurized liquid extraction (PLE)? Explain the choice of method chosen and why the other method is not suitable.
- If you were to analyse caffeine in a coffee drink, which sample preparation method is more suitable, solid phase microextraction (SPME) or solid phase extraction (SPE)? Discuss the reason for your choice and the reason for not choosing the other method.
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- What are the advantages and disadvantages of using external standards in instrumental analysis?You are an aquatic scientist and tasked to sample water that contains chlorophenols for gas chromatographic analysis from your local waste water treatment plant (WWTP). Using knowledge of sample preparation and chromatograph, how would you sample, preserve and prepare these samples for GC analysis and why GC is the best detection technique?What are the differences between systematic and random errors and how do they effect accuracy and precision? In what circumstances would you use standard addition (versus a normal calibration curve) to determine the amount of an analyte in a sample? A urine sample, containing analyte Z is analysed by the standard addition method where 5 mL of the original sample was mixed with increasing amounts of a Z standard and each solution diluted to a volume of 50 mL prior to analysis. A plot of the final concentration of the standard in each of the 50 mL samples (x axis) versus The measured signal from the analysis of each 50 mL sample (on y axis) produced a straight line with the general equation: y = 44.72x + 4.06 what was the final concentration of Z in the 50 mL standard addition sample? what was the initial concentration of Z in the original urine sample?
- Can paper chromatography be used to separate and identify very volatile substances? Why? Please explain comprehensively.Why is strict implementation of LQMS (Laboratory Quality Management System) or GLP is necessary ? What are the elements ?Why chromatography is an important tool for analysis of organic compounds?
- A chemist received a radioactive sample that is suspected to contain U, 23U and other elements. The authority wants to know the distribution, qualitative and quantitative composition of the sample. Propose with justifications, ONE Surface analysis technique that can be performed on this sample.One method for quantitative determination of the concentration of constituents in a sample analyzed by gas chromatography is the area normalization method. In this method, complete elution of all of the sample constituents is necessary. The area of each peak is then measured and corrected for differences in detector response to the different eluates. This correction is accomplished by dividing the area by an empirically determined correction factor. The concentration of the analyte is found from the ratio of its corrected area to the total corrected area of all peaks. For a chromatogram containing three peaks, the relative areas were found to be 16.4, 45.2, and 30.2 in the order of increasing retention time. Calculate the percentage of each compound if the relative detector responses were 0.60, 0.78, and 0.88, respectivelyOne method for the quantitative determination of the concentration of constituents in a sample analyzed by gas chromatography is area normalization. Here, complete elution of all the sample constituents is necessary. The area of each peak is then measured and corrected for differences in detector response to the different eluates. This correction involves dividing the area by an empirically determined correction factor. The concentration of the analyte is found from the ratio of its corrected area to the total corrected area of all peaks. For a chromatogram containing three peaks, the relative areas were found to be 16.4, 45.2 and 30.2, in order of increasing retention time. Calculate the percentage of each compound if the relative detector responses were 0.60, 0.78 and 0.88, respectively.
- In a volumetric determination of an analyte A, the data obtained and their standard deviations are as follows: Initial buret reading 0.19 mL 0.02 mL Final buret reading 7.86 mL 0.03 mL Sample mass 63.0 mg 0.2 mg From the data, find the coefficient of variation of the final result for the %A that is obtained by using the equation that follows and assuming there is no uncertainty in the equivalent mass. %A= titrant volume x equivalent mass x 100 %/ sample mass Coefficient of variation = Submit Answer % Try Another Version 10 item attempts remainingIn a Bradford assay, 11 µl of a protein isolate sample was diluted by adding 21 µl of water prior to the addition 2.0 mL Bradford reagent. Calculate the protein concentration (in mg/mL) of the original protein isolate sample whose absorbance reading at 595 nm is 0.304 after dilution. The protein standard solutions used for the calibration curve of the Bradford assay was constructed using bovine serum albumin (BSA) stock solution whose concentration is 200 µg/mL. The concentration and the corresponding absorbance reading at 595 nm of the protein standard solutions are summarized in the table below: Standard soln # 1 2 13 4 6 conc of BSA 12.00 24.00 36.00 48.00 60.00 (pg/mL) Absorbance at 595 nm 0.000 0.156 0.249 0.328 0.411 0.528 zNote: Final answer format must be x.xxx (three decimal places). Round off only in the final answer. Do not round off in the middle of the calculation.As part of an analytical chemistry laboratory course, a student measured the Ca2+ content in two water samples, city-supplied drinking water and well-supplied drinking water, using two different analytical methods, flame atomic absorption spectrometry (FAAS) and EDTA complexometric titration. The results of this experiment are given in the table as the mean Ca2+concentration (?¯) and standard deviation (?) in parts per million (ppm). Each sample was measured five times (n=5) by each method. Method City-Supplied Drinking Water (?¯±?x¯±s) Well-Supplied Drinking Water (?¯±?x¯±s) FAAS 57.57±0.68 ppm 64.77±0.70 ppm EDTA titration 58.32±0.96 ppm 65.62±0.97 ppm Method Comparison: For each drinking water sample (city and well), compare the Ca2+ content measured by FAAS and EDTA titration. Calculate the ? value for each sample. Do the methods produce statistically different results at the 95% confidence level when measuring the Ca2+content of the city-supplied drinking water? Do the…