A5.12-g pesticide sample was decomposed and then dilute to 200-ml to determine its Cu" contents. The analysis was completed by treating aliquots as indicated: Volume of sample, mL Volume of 3.82 ppm Cu2", mL Signal 50.0 0.00 0.512 50.0 4.00 0.844 a. Calculate the percentage of copper in the pesticide sample. b. What assumption did you make in calculating the concentration of copper in your sample?
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- A second spectrophotometric method for the quantitative analysis of Pb2+ in blood yields an Ssamp of 0.712 for a 5.00 mL sample of blood. After spiking the blood sample with 5.00 μL of a 1560 ppb Pb2+ external standard, an Sspike of 1.546 is measured. What is the concentration of Pb2+ in the original sample of blood?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…
- 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…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 equationsChemistry The levels of an organic pollutant (P) in the groundwater at the perimeter of a plant were a cause for concern. A 10 mL sample of the water was taken and the pollutant was extracted with 95% efficiency using 25 mL of diethyl ether. GC was used to analyse the concentration of P in diethyl ether. A calibration curve was plotted for a series of standards of P which yielded the following results: Peak Area Toluene Conc. (µg/ml) 12,000 2.6 23,700 5.0 35,500 7.7 46,800 9.9 31,250 Sample Determine the concentration of P in ppb in the initial groundwater sample.
- Which statements are TRUE regarding internal standards? I. The response factor is calculated by using a mixture containing known amounts of analyte and internal standard and by using detector response to the analyte and the internal standard. II. Internal standards are useful where instrument response or quantity of sample analyzed varies over time. III. Detector response is inversely proportional to concentration. IV. Detector response to analyte and internal standard is assumed to be constant over a range of concentrations A. I, II, and III B. II, III, and IV C. I and II D. I, II, and IVA 0.500g sample is analyzed spectrophotometrically for manganese by dissolving it in acid and transferring to a 250 mL flask and diluting to volume. Three aliquots ae analyzed by transferring 50 mL portions with a pipet to 500 mL Erlenmeyer flask and reacting with an oxidizing agent, potassium peroxydisulfate, to convert the manganese to permanganate. After reaction, these are quantitatively transferred to 250 mL volumetric flasks, diluted to volume and measured spectrophotometrically. By comparison with standards, the average concentration of the final solution is determined to be 1.25 x 10^-5M. What is the percent manganese in the sample?A 5.00 (±0.01) mL5.00 (±0.01) mL Class A transfer pipet is used to transfer 5.00 mL5.00 mL of a 0.253 (±0.003) M0.253 (±0.003) M Cu2+Cu2+ stock solution to a 100.00 (±0.08)100.00 (±0.08) Class A volumetric flask. Deionized water is used to bring the flask to volume. Calculate the concentration of the diluted soluion in the volumetric flask and report its absolute uncertainty.
- A new method is proposed to simultaneously detectand separatefour foodadditives by reversed-phase liquid chromatography. The data were obtained using theliquid chromatographic column with a flow rate of 0.5 mL per min and with the followingparameters: Pore size 100 A Particle Size 3.5 Internal diameter 4.6 mm Length 150 mm The food additives found in the sample resulted in the following data: ( see image for table) a.Calculate the number of plates from each peak. b.Calculate the plate height for the column. c.Retention factor for each peak.A volume of 250 ml of a 0.05 M solution of a reagent of formula weight (relative molecular mass) 40 was made up, the weighing being done by difference. The standard deviation of each weighing was 0.0001 g. 1 (a) What were the standard deviation and relative standard deviation of the weight of reagent used?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