Gravametric Quant Lab Report

Quantitative outline gravimetric mark of Iron as Fe2O3 testing ground Experiment 2 February 19, 2013 Abstract In the Gravimetric determination is the mensuration of mass in two disparate forms precipitation and volatilization. In our experimentation we will be using the precipitation form which isolates an ion in a dissolver by a precipitation reaction, sieveing, purifying by scour method, conversion to harvest-time of known composition, and lowest weigh of the product canvass the mass difference of theorictal and actual. This method identified the weight sh atomic number 18 of beseech in an unknown sample. one-third samples are taken to limit share error. In the results of the three samples 1 had a per centum of 10. 764 Fe (III), sample 2 had a percent of 11. 725 Fe (III), and sample 3 with a percent of 12. 216 Fe (III). The average sample percent was 11. 568 compared to minded(p) amount percent of 12. 90. In theory with a exit of 1. 332 this experiment was over i n all successful. instauration In this lab the purpose was to use the gravimetric determination map to identify the weight percent of iron in an unknown sample. Three samples were collected and analyzed.Iron can be analyzed by precipitating the supply iron oxide from a basic solution. After the basic solution is render the process is then followed by ace dehydration to give immobile iron oxide. Methods and Materials Needed in the experiment was * crucibles, Metal rings, Wire triangles, Burners, Funnels, imbue Paper, Beakers, Glass rod, Diluted ammonium hydroxide solution, Nitric acid solution, silver-tongued nitrate solution, NH4NO3 solution, Distilled weewee. Below are some methods used in experiment. fig. 1 fig. 2 Experimental Procedure This experiment was a multiple posing lab.Obtain three melting pots and desiccator. Bring the three porcelain crucibles and caps to regular mass by oestrus to redness for 15 minutes over a burner, use fig. 1 for method reference. Pl ace the heated crucibles in the desiccator to cool for approximately 30 minutes and weigh. This was left overnight and completed the second trial in the next session with successive weighing agreed within 0. 30mg. (Keep constant numbering with crucibles throughout experiment) We measured out 1. 5g of three samples of the unknown that was given to us. Each sample was dissolved in 10 mL of 3M HCl (with hotness necessary). mL of 6 M HNO3 was obtained to filtrate, and boil for a few minutes to ensure that all iron is oxidized to Fe (III). The samples was hackd to 200mL with distilled water and add 3 M ammonia with constant stirring until the solution was basic (as determined with pH indicator report card). After solution becomes basic, accept the lessen by boiling for 5 minutes and allow the precipitate to settle. We then decanted the supernatant liquid through coarse, ash less filter paper (Whatman 41 or Schleicher and Schuell Black Ribbon, as in fig. 2 -18 and 2 -19 in textbook. ). Keep liquid lower than 1 cm from the top of the funnel.Our precipitate was first muteed repeatedly with hot ammonium hydroxide solution, by miscommunication. Then washed with the corrected heated ammonium nitrate and left it to drain overnight until next session. We continued to wash supernatant until little or no Cl- is detected in filtered supernatant. chance the Cl- by acidifying a few milliliters of filtrate with 1 mL of dilute HNO3 and adding a few drops of 0. 1 M AgNO3. If precipitate is observed, Cl- is present. After identifying that at that place was not any Cl- present we allowed the filter to drain overnight cover with ventilation.Carefully, the paper was lifted out of the funnel, folded (fig. 2), and transferred all dried substance to crucible and any substance that is not completely dry place into beaker and into the sens for half an hour. Those situated in beaker was then placed into the crucibles that were brought to constant mass. With the paper and substanc e in the crucible it was placed over a olive-sized beam with the lid off to start to char the filter paper. The flame temperature was then increased keeping the lid handy to smother the crucible of the paper flames.After the paper seems visibly charred ignite the product for full 15 minutes with full heat of the burner directed at the base of the crucible where oxidized iron is located. When the crucibles have briefly cooled in the air, we then placed them in the desiccator for 30 minutes. After the 30 minutes of cooling in the desiccator weigh the crucible and the lid, reignite, and bring to constant mass with the repeated change within a mass of 0. 3 mg. We are now complete with the experiment. Calculate the weight percent of iron in each sample, the average, the well-worn deviation, and the relative standard deviation for your data.Results Crucible 1 0. 231 g Fe2O3 ? 1 mol Fe2O3159. 487g ? 2 mol FeOOH1 mol Fe2O3? 55. 845 g1 mol = 0. 162g Fe0. 162 g1. 505 g? deoxycytidine mo nophosphate=10. 764% Crucible 2 0. 252 g Fe2O3 ? 1 mol Fe2O3159. 487g ? 2 mol FeOOH1 mol Fe2O3? 55. 845 g1 mol = 0. 176g Fe0. 176 g1. 501 g? 100=11. 725% Crucible 3 0. 268 g Fe2O3 ? 1 mol Fe2O3159. 487g ? 2 mol FeOOH1 mol Fe2O3? 55. 845 g1 mol = 0. 183g Fe0. 183 g1. 502 g? 100=12. 216% *Refer to appendix for sample mass table and deliberateness equations Crucible 1 Crucible 2 Crucible 3 fish percent 10. 764 % 11. 725 % 12. 216%Average 0. 250 g Standard deflection 0. 019 Relative Deviation 0. 015 Discussion Since the obtained and expected results are not 100 percent first mate we can conclude that during the experiment we encountered a loss of product, with an average percent of 11. 57 and an obtained of 12. 90 percent. In the experiment the precipitate was washed repeatedly with given solution to filter out any Cl- at this clock time we commemorate that some of the precipitate had gone through the filter through the sides from solution being held to high causing an overflow o n the sides of the filter.This was notice by the orange tint in the beaker of the filtered solution. In the experiment scales were besides changed due to overuse. That could cause some flux in the measurement changes by small degree. Another error or issue during the experiment a lids on our crucible broke having to replace it caused a changed in our final weigh being that in the beginning we weighed our crucibles with the lid. Remaining constant in the lab is a must this does cut back on experimental error such as using the same analytical balances and labeling all equipment and crucibles.In the Gravimetric determination is the measurement of mass in two different forms precipitation and volatilization. Some of the underlying principles and theories of gravimetric analysis are police of mass action, reversible reactions, and principle of solubility product and common ion effect. terminus The gravimetric determination procedure determined that we had an average of 11. 568% of Fe in our unknown solution, given the amount of 12. 90% of Fe. We experienced a loss of approximately 1. 332 %. This loss could be included in instrumental and serviceman errors.References Lewis, D. 2013. Quantitative Analysis Lab Journal. Gravimetric Determination of Iron as Fe2O3. Vol. 1 Pages 4 5. Franklin, J. 2013. Quantitative Analysis Lab Journal. Gravimetric Determination of Iron as Fe2O3. Vol. 1 Pages 7 11. Bb Learn. 2013. Quantitative Chemical Analysis. Gravimetric Determination of Iron Lab Handout. Harris, Daniel C. 8th edition. Quantitative Chemical Analysis Textbook. Appendix Calculation equations Mean Mean = Sum of X set / N(Number of values) Standard Deviation Relative Deviation 100 ? sxCrucibles mess of the Beaker (empty) (g) Mass of the Beaker & Unknown (g) Mass of the Unknown Sample (g) 1 144. 181 g 146. 686 g 1. 505 g 2 159. 328 g 160. 829 g 1. 501 g 3 167. 480 g 168. 982 g 1. 502 g * Above are the measurements of the unknown samples obtained Crucibles Mass of Crucible (g) Mass Crucible & final product (g) Mass of final product (g) 1 31. 752 g 31. 982 g 0. 231 g 2 33. 820 g 34. 072 g 0. 252 g 3 40. 802 g 40534 g 0. 268 g * Above are the measurements of Iron found in unknown sample