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PAGE 1 * PAGE 2 * Page 3 * PAGE 4 * PAGE 5 * PAGE 6 * PAGE 7 * page 9 from the Futures Language School, Cairo * EMAIL Dr Mahmoud Marsafy * back to Dr M's index * doc b email query?comment REMEMBER: you must do your own experiment risk assessment, ideas are illustrated but health and safety details are NOT included
24. The Displacement of Copper from Copper(II) Sulphate Solution using Zinc
The CHART A above introduces an attempt to
investigate the stoichiometry of the important cationic spontaneous redox
replacement reaction for Zn(s) immersed in Cu2+(SO42-)
solution. It introduces the utilisation of a remarkable pocket size sensitive
balance (100 gram load & precision of 10 mg). In my opinion, such type of
balance could well substitute all the expensive sensitive balances being
utilised now in schools. The balance is very affordable, price-wise. I bought
it in Cairo for about 20$. Also a small electric hot plate of very low wattage
is used for evaporation to dryness of solution supernatants, coupled with
accurate weighing of the residue. Further the reaction has been accomplished in
1 ml solution containing ONE MILLI-MOLE of Cu2+.
Reactivity Series of Metals including displacement reactions and an introduction
to redox reactions
The reaction is driven to completion in a short time (about 10 minutes). To achieve this, the reaction is carried out at about 70Co, by heating on a small (12W) electric plate .The original blue solution does not boil under these conditions. The completion of the reaction is clearly indicated by the full decolorisation of the original solution. (Chart B)
All the products of the complete reaction are separated quantitatively, i.e. both the ZnSO4, replacing the original CuSO4, and the resulting solid copper, characterized by its reddish brownish colour. (Charts C&D) Reactivity Series of Metals including displacement reactions and an introduction to redox reactions
The separation of the products: the supernatant colorless ZnSO4 solution & the spongy reddish brown precipitate of Cu metal is achieved by a decantation technique. The supernatant solutions, as well as the subsequent washings are removed quantitatively by careful manipulation and by suction with a thin, long stem plastic dropper. Thus avoiding the laborious conventional filtration technique. To recover the solid ZnSO4 the supernatant solution was evaporated to complete dryness in a vial heated by a gas flame. The vial was loosely capped by an Aluminium small sheet to prevent loss of the product at the end, by being ejected out of the vial. It was then transferred to a weighed aluminium sheet, to measure its mass with the sensitive small balance. C. Similarly the copper deposit was carefully dry heated after washing and discarding the washings, and the dried mass was determined. (CHART C)
Reactivity Series of Metals including displacement reactions and an introduction to redox reactions
The 1 milli-mole Cu2+ solution in 1ml water was prepared by weighing exactly 250 mg CuSO4.5H2O s, in a vial and dissolving in 1 ml water. The solution has to be heated for complete dissolution. (Chart E) Note: Heating could also be achieved by the electric hot plate, or hot water could be added from the start. The 1ml of water was manipulated by a graduated plastic syringe with its needle removed.
The following table summarises the experimental results and compares these results with those predicted from the reaction equations.
* 250 mg copper sulphate pentahydrate (CuSO4.5H2O) s was dissolved in 1 ml water. These deviations from the anticipated values are due to limitations in the experimental technique adopted: · The sensitive balance utilized has a sensitivity of 10 milligrams. It is suggested that improvements would be achieved by using a sensitive balance of 1mg accuracy. · The use of one milli-mole of copper sulphate solution is restricting the accuracy of the results of the reacting masses. Therefore it is recommended to use five milli-moles of CuSO4(s) to overcome these limitations. It is recommended also to change the vials utilized in this investigation, and replace them with vials with wide upper openings, and also wider bottoms. Also to use a low wattage Electric Hot Plate (12 watts) for evaporating to dryness the solutions until constant weighs. This modification is expected to reduce the errors due to abrupt violent boiling towards the end of evaporation, which causes ejection of the residual solids out of the vials. The heating of the copper deposit under these conditions will not cause any oxidation to copper oxide, as would happen if it is dried using normal Bunsen burners. The evaporation of the solutions heated by this hot plate in wider top vials, or small beakers is expected to proceed at the approximate rate of 2.5 ml per hour. The evaporated solution will never boil under these conditions until complete dryness.
Reactivity Series of Metals including displacement reactions and an introduction to redox reactions
The full replacement of the Cu2+ ion with Zn2+ ion is verified by the reaction of a drop of the original and final supernatant solutions with a drop of ammonia solution, in separate cavities of a multi-cavity plastic strip. (Chart F) Chart F includes also an extension experiment where the displacement of Cu2+ (aq) ion is achieved by use of an iron nail.
Summary of the experiment
Reactivity Series of Metals including displacement reactions and an introduction to redox reactions
* PAGE 2 * Page 3 * PAGE 4 * PAGE 5 * PAGE 6 * PAGE 7 * page 9 from the Futures Language School, Cairo * EMAIL Dr Mahmoud Marsafy * back to Dr M's index * doc b email query?comment |
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drmm8 updated Mar 23rd 2008 |