A UVisible spectrophotometer was zerced with distilled water at $10 nm, using a s The absorbances of four standard Co() solutions were then measured at the same table below indicates the data. Calculate the moler absorptivity (e) by considering ALL the dete in your calculation Col)] mol dm O 1.06-03 2.06-03 4.0E-03 8.06-03 Absorbansie / Absorbance 017 0.58 097

A UVisible spectrophotometer was zerced with distilled water at $10 nm, using a s The absorbances of four standard Co() solutions were then measured at the same table below indicates the data. Calculate the moler absorptivity (e) by considering ALL the dete in your calculation Col)] mol dm O 1.06-03 2.06-03 4.0E-03 8.06-03 Absorbansie / Absorbance 017 0.58 097

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

Chapter14: Applications Of Ultraviolet-visible Molecular Absorption Spectrometry

Section: Chapter Questions

Problem 14.12QAP

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In the development o f an analytical method for the quantitative analysis o f iron using Atomic Absorption spectrophotometry (AAS), a linear calibration curve for standards o f 0.00, 5.00, 10.00, 15.00 and 20.00 ppm was prepared. An iron ore sample with an expected iron content o f 40-60% w/w is to be analysed by this method. An approximately 0.5-g sample is taken, dissolved in a minimum amount o f concentrated HC1 and diluted to 1 L in a volumetric flask using distilled water. A 5.00-mL aliquot is removed with a pipette. With explanation, to what volume (10, 25, 50, 100, 250 500 or 1000 mL) should the 5.00 mL aliquot be diluted, to minimize the uncertainty in the analysis?
Determine the relationship between the observed/apparent value (EX) VERSUS that of the true value (ET) for the quantity being sought by writing either <, >, or = on the space provided Determination of the true concentration (ppm Fe) in a water sample using the iron-phenanthroline method. Dilution factor was not taken into account. EX _____ 1ET
Using the absorbance of [FeSCN]+2 at the wavelength of maximum absorption which you obtained in part B, and the diameter of the tube, obtained in part A,calculate the molar extinction coefficient. given info: Concentration of Fe3+ stock solution, C1 = 0.001 M Volume of stock Fe3+ solution pipetted, V1 = 25mL Concentration of diluted stock solution, C2 = 0.0004 M Volume of Fe2+ solution and KSCN (upon mixing) = 10mL Weight of KSCN = 1g The reaction taking place is given as: The reaction taking place is given as: F e 3+ (aq) + SC N − (aq) ⇔Fe [SCN] 2+ (aq) the concentration of [FeSCN]2+ after the mixing of Fe3+ and SCN- is 2.5 x 10-3 M. Moles of [FeSCN]2+ = 2.5 x 10-5 moles Diameter:1.2cm The wavelength at which maximum absorption takes place is = 480 nm
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…
For bulk crystalline sample which technique is best ? Give me handwritten answer with explaination?
A sample of iron ore weighing 800 mg was treated with HNO3 , boiled to dryness and redissolved in dilute HCl. After filtration and removal of undissolved silica, the liquid was passed through a Walden reductor. The collected sample was titrated with 0.0210 M KMnO4 , requiring 12.0 mL to reach the end point. Calc %Fe (55.845) in the ore.
The absorbance of an iron thiocyanate solution containing 0.00500 mg Fe/mL was reported as 0.4900 at 540nm. Calculate the specific absorptivity including units of iron thiocyanate on the assumption that a 0.100 cm cuvette was used.
Why is glass better than fused silica as a prism construction material for a monochromator to be used in the region of 400 to 80 nm?