Question

Lab procedure: This laboratory exercise involves the use of dilute sulfuric acid (H2SO4) to leach...

Lab procedure:

This laboratory exercise involves the use of dilute sulfuric acid (H2SO4) to leach copper from a synthetic copper-containing ore, malachite. This technique is known in the mining industry as solution mining. The soluble copper is then filtered to remove unreacted ore (the residue) from the filtrate containing the copper+2 ion. The copper in the filtrate is then treated with metallic magnesium to precipitate the copper as the familiar orange-brown metal. This copper is dried and weighed. From these data the percent copper in the original ore can be determined. In this experiment you will use many of the concepts and techniques you have already learned in class including: molar mass calculations, separation by dissolution, oxidation-reduction, precipitation, equation writing and balancing, reaction types, activity series, percent composition, and percent error.

-Using an electronic balance weigh out approximately 2.5-3.0 grams of the green malachite ore. The ore may be dusty so avoid breathing in the dust. Place this ore in a 250-mL beaker and add very slowly 20 mL of 2M H2SO4. Since the malachite contains a metal carbonate, you can expect significant foaming and gas evolution. Using a glass stirring rod mix the ore with the acid. Dilute this copper-containing solution with 25 mL of deionized water.

- Decant this solution into a funnel equipped with a 12.5 cm filter paper circle. Place another 250 mL beaker beneath the funnel. Once most of the blue-green colored copper solution has passed through the filter, wash the residue (unreacted ore) in the beaker with 10-15 mL of deioned water. Add this washing to the filter paper in the funnel. You may want to test the residue in the beaker by adding 5 mL of 2M H2SO4 to see if any additional copper can be removed from the ore. If the acid solution in the beaker turns blue-green, more copper has been extracted and you will need to add this solution to the filter. Once the filter has completely drained, discard the filter paper.

-To the filtrate, add.0.40-0.50 grams of magnesium turnings. You will notice gas evolution and an immediate precipitation of copper metal. The colored solution will fade to a colorless solution. The magnesium will react with any unreacted sulfuric acid in the filtrate to liberate a gas. If a blue-green color persists, add an additional piece of magnesium turnings until the solution has been completely decolorized. If after the evolution of gas has ceased and there appears to be be any magnesium remaining, add 1-2 mL of 2M H2SO4 to completely remove residual magnesium.

-Transfer the precipitated copper to a piece of pre-weighed filter paper in a funnel using a stirring rod equipped with a rubber policeman. Wash the copper with 15-25 mL of deionized water and discard the filtrate. Place the copper on the filter paper on a watch glass and place it in an oven at 100 ºC.

-After drying the copper for 15-20 minutes, weigh the copper and filter paper and determine the mass of copper you have recovered.

Lab questions:

What gas was evolved when the ore was treated with the acid?

Did the copper appear the same before and after drying? If not, what can account for the color change? Write the equation for this color change. How will this affect the percent of the recovered copper?

1 0
Add a comment Improve this question Transcribed image text
Answer #1

Malachite, one of the common copper ores which is composed of copper carbonate, CuCO3.Cu(OH)2 mainly ,when sulfuric acid is added to malachite,it produces copper oxide along with the release of carbon dioxide.

CuCO3.Cu(OH)2 → 2 CuO + CO2+ H2O

and 2 CuO + C → 2 Cu + CO2

Hence the gas was evolved when the ore was treated with the acid was CO2.

No, the copper did not appeared the same before and after drying.If the sample appears to be black in color, then it means that the copper is too much heated and copper (II) oxide has been formed.

The reaction involved for the color change;

2 Cu + O2 → 2 CuO

this will affect the percent of the recovered copper by increasing the mass of Cu of the final product. As we know

percent recovered =  (mass of final product / mass of initial sample ) 100

so if mass of final product is increased due to copper (II) oxide, the percent recovered will be more ,hence giving wrong result of the experiment.

hope this is helpful!

Add a comment
Know the answer?
Add Answer to:
Lab procedure: This laboratory exercise involves the use of dilute sulfuric acid (H2SO4) to leach...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • THE EMPIRICAL FORMULA OF SELECTED HYDRATES experiment PROCEDURE THIS EXPERIMENT SHOULD BE DONE IN PAIRS. 1....

    THE EMPIRICAL FORMULA OF SELECTED HYDRATES experiment PROCEDURE THIS EXPERIMENT SHOULD BE DONE IN PAIRS. 1. Available to you should be: a Büchner funnel, a rubber funnel adapter, side-arm filter flask, thick-walled rubber tubing, plastic forceps and a plastic spatula. 2. Before you turn the hotplate on, wipe the hotplate down with a damp paper towel. During this experiment you will be placing filter paper containing products directly onto the surface of the hotplate. As such, you will want to...

  • ALL THE INFO YOU NEED IS BELOW average volume of NaOH: 15.7 mL or 0.0157 L...

    ALL THE INFO YOU NEED IS BELOW average volume of NaOH: 15.7 mL or 0.0157 L average number of moles of NaOH added: 6.28*10-4 moles molar concentration of [HT] in saturated solution(HT– acts as a monoprotic acid, reacting with NaOH in a 1:1 ratio (Volume of KHT measured using 25.00 mL volumetric pipet.)): 0.2512 M Analysis of KHT in water 1. Weigh out 0.8 grams of potassium hydrogen tartrate (KHT) on weighing paper. Add the KHT to a clean dry...

  • for this experiment of syntheis of aspirin, was the product obtained pure (based on color)? how...

    for this experiment of syntheis of aspirin, was the product obtained pure (based on color)? how do you know? the color was white Experimental Procedure HAZARD: Sulfuric acid, acetic anhydride and glacial acetic acid are corrosive to the skin. They are also irritants, and all operations in which these substances are used should be carried out under the hood. Prepare a hot-water bath by heating a 400-ml beaker containing about 200 mL of water. 1. Use a centigram balance and...

  • based on data please help fill out chart and questions 1,2,3 Part II: Neutralization of the...

    based on data please help fill out chart and questions 1,2,3 Part II: Neutralization of the Tablet 1. Obtain one of the commercial antacid tablets that your Lab Instructor has assigned you. 2. Weigh and record the weight of the tablet. 3. Crush the tablet using mortar and pestle. 4. Transfer as much of the crushed tablet as you can onto a weigh boat. 5. Weigh the tablet and weigh boat, and record this value. 6. Pour the entire contents...

  • Calculate the % Al in the sample. Preparation of a stock solution of aluminum Accurately weigh...

    Calculate the % Al in the sample. Preparation of a stock solution of aluminum Accurately weigh out approximately 1 g of the aluminum foil. Tear it up into small pieces, place the pieces into a covered 250 mL beaker and add 60 mL of 6M HCl. This should be carried out in the fume hood because the reaction is exothermic and leads to violent frothing and emission of vapors. Cool, quantitatively transfer to a 250 mL flask, rinsing with deionized...

  • What is the percent yield of the lab procedure below? my final weight of the product is 0.0519 g

    what is the percent yield of the lab procedure below? my final weight of the product is 0.0519 g sure of the proper disposal methodl, properly Check with your laboratory insructor if you are PROCEDURE Be sure to dry the 5-mL reaction vial in the oven for at least twenty minutes. Water is experiment. this Preparation of the Ylide 1. Place 0.480 g of benzyltriphenylphosphonium chloride in a dry, 5-mlL reaction vial containing a magnetic spin vane Add 2 mL...

  • please help fill out chart and questions based on the information given, please help fillout chart...

    please help fill out chart and questions based on the information given, please help fillout chart and calculations, all information is given Part II: Neutralization of the Tablet 1 Group) 1 Antacid tablet brand Mass of whole tablet 8 Tums 5.6432 7.3013 2. 1673 g Mass of weighing boat and tablet Mass of weighing boat following transfer 8 Mass of crushed tablet used 8 Part III: Titration of Simulated Stomac Acid (without antacid) Trial 1 Trial 2 Volume HCl used...

  • CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the...

    CHROMIC ACID OXIDATION Pre Lab Questions the amounts of materials that will be used from the experimental section above) H2SO4 + Na2Cr207 2H20- H2O, A Molecular Weight Theoretical yield amount moles on (if applicable) Equivalents 2. Look up the melting point for p-nitrobenzoic acid and record the reference. 3. What color change is expected to be observed in the reaction? Explain why. CHROMIC ACID OXIDATION Experimental Procedure: Part I: Synthesis of p-nitrobenzoic Acid 1. Under the hood, add 0.400 g...

  • PROCEDURE CAUTION!!! Nitric acid and sulfuric acid are strong and corrosive acids. For that reason, avoid...

    PROCEDURE CAUTION!!! Nitric acid and sulfuric acid are strong and corrosive acids. For that reason, avoid inhaling its vapors or causing any contact with the skin or clothing. Wear your protective glasses at all times. Use the extractors to work with these acids. A. Nitration of methyl benzoate 1. Preparation of the reactants. In the extractor you will find a burette with concentrated sulfuric acid, a second burette with concentrated nitric acid, clearly identified. Familiarize yourself with the scales of...

  • Experiment 17A. A Solubility Product Constant Procedure Getting Started 1. Obtain a 10 ml pipet, ...

    question#1 Experiment 17A. A Solubility Product Constant Procedure Getting Started 1. Obtain a 10 ml pipet, a 50 mL buret, and 2 pieces of 120 cm filter paper Preparing Saturated Solutions of M10J MIO), is an insoluble divalent iodate salt. The identity of the cation M-is unknown. 1 Prepare MIO,), by adding S0 ml of o.2 M KIO, to 20 mL of 1 Molar M(NO,J, in a 150 mt 2. Stir the mixture vigorously with a stirring rod. A white,...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT