Copper (II) chloride
Chemical formula | CuCl2 |
---|---|
OTP appearance | yellow-brown solid |
Molar Mass(g/mol) | 134.45 |
Density(g/cc) | 3.386 |
Melting Point(°C) | 498 |
Boiling Point(°C) | 993 (decomp) |
Solubility in water(g/L) | 757 |
Solubility in ethanol(g/L) | 530 |
Solubility in methanol(g/L) | 680 |
Solubility in ether(g/L) | 1.1 |
Solubility in acetone(g/L) | 30 |
NFPA 704 |
|
Thermal Decomposition | copper (II) chloride
993°C CuCl,Cl2 |
Uses
Other
- Catalyst for the production of sulfuric acid
- Metal Etchant
Natural occurrence
Hazards
Soluble copper compounds are toxic to mammals and can be deadly to fish.
Production
Synthesis
The main routes are divided by the source of the chloride ion. The simplest is hydrochloric acid:
via chlorine
metallic copper
At or above red heat (~500°C), copper reacts directly with gaseous chlorine, giving molten CuCl2. The reaction is sufficiently exothermic that the reaction will continue once started.
via hydrochloric acid
metallic copper
- Bubble air through copper metal immersed in hydrochloric acid. This will not work without the air, and even then it takes days. This may go in two separate steps, first to copper (I) chloride, and thence to copper(II) chloride, shown separately below.
- 4 Cu + 4 HCl + O2 → 4 CuCl + 2 H2O // from copper(0) to copper (I)
- 4 CuCl + 4 HCl + O2 → 4 CuCl2 + 2 H2O // from copper(I) to copper (II)
copper (II) minerals
- Combine malachite and hydrochloric acid
- Cu2(OH)2CO3 + 4 HCl → 2 CuCl2 + 3 H2O + CO2
copper (I) chloride
- Bubble air through copper (I) chloride in hydrochloric acid. This will not work without the air, and even then it takes days. [1]
- 4 CuCl + 4 HCl + O2 → 4 CuCl2 + 2 H2O // from (I) to (II)
via sodium chloride
water | ethanol | |||
---|---|---|---|---|
g/L | M | g/L | M | |
copper chloride | 757 | 5.63 | 530.00 | 3.94 |
sodium chloride | 359 | 6.10 | 0.65 | 0.01 |
copper acetate | 65 | 0.36 | 71.40 | 0.39 |
sodium acetate | 1233 | 15.00 | 23.00 | 0.28 |
copper sulfate | 200 | 1.26 | ins | 0 |
sodium sulfate | 139 | 1.02 | ins | 0 |
copper (II) acetate
- 0.035M (100ml) scale
- Gather 7g (0.035M) of copper (II) acetate monohydrate
- Heat to 160°C (325F) for 10 minutes to drive off the water
- Measure mass again: should be 6.35(7)g (0.035M)
- Dissolve in 100ml dried ethanol (saturated limit, 0.35M)
- Transfer ethanol to separation funnel
- Prepare saturated saline solution (6M)
- Repeat
- Add 5.7ml of saturated saline solution to ethanol in sep funnel, shaking regularly
- Draw off aqueous layer and evaporate
- NB: Should contain mostly sodium acetate, less sodium chloride.
- Until mostly sodium acetate remains
- Evap the ethanol layer, leaving mostly copper chloride
When using salt as a source of chlorine, choose an anion whose copper salt that is more soluble in water than ethanol, such as copper (II) acetate or copper sulfate, and preferably an anion for which the sodium salt also prefers water. Mix them in a water/ethanol solution, and allow the copper chloride to dominate the ethanol phase.
via ammonium chloride
...hydrochlorination of the copper(II) compounds begins at 190°C to form ammonium chlorocuprates, (NH4)2CuCl4 in with copper (II) oxide and NH4CuCl3 with copper (II) sulfide, which at the temperature higher than 300°C decompose affording CuCl2[2]
- Combine (dry) ammonium chloride and copper (II) oxide in a flask
- Direct gasses from flask through CaO dryer, then a suckback trap, and thence to a water bubbler.
- Heat to 190°C
- 4 NH4Cl(s) + CuO(s){(NH4)2CuCl4(s) + NH4OH(g) + NH3(g) // gasses condense or are absorbed by water190°C}→
- 4 NH4Cl(s) + CuO(s)
- remove dryer
- Heat to 300°C
- (NH4)2CuCl4{CuCl2(s) + 2 NH4Cl(g) // may condense in trap or be absorbed in bubbler300°C}→
- (NH4)2CuCl4{CuCl2(s) + 2 NH3(g) + 2 HCl(g) // may recombine to 2 NH4Cl in trap, or be absorbed in bubbler.338°C}→
- (NH4)2CuCl4
- Remove bubbler
- Cool to RT with dryer in place.
Purification
recrystallize from hot dilute aqueous HCl by cooling in a calcium chloride-ice bath
Storage
- Do not store with excess copper. This can result in decomposition to copper (I) chloride:
- Cu + CuCl2 → 2 CuCl
- Do not store in acidic conditions.
Disposal
- Combining with sodium hydroxide produces insoluble copper hydroxide, which will then absorb carbon dioxide from the air, resulting in nature-safe carbonate/hydroxide compounds equivalent to malachite and azurite
- Combining with sodium bicarbonate or sodium carbonate shortcuts the carbon dioxide absorption and produces the mineral forms of copper directly.
See Also
- US patent 2587579 "Method of production of cuprous oxide and copper chlorides"
Link courtesy Google - Borisov, V. A.; D’yachenko, A. N.; Kraidenko, R. I. (2011) "Reaction of ammonium chloride with the copper(II) sulfide and oxide, and identification of the reaction products"
Russian Journal of General Chemistry 81(7); pp1430-1433.
DOI:10.1134/S107036321107005X</ref>
References
- ↑ US patent 2586579 "Method of production of cuprous oxide and copper chlorides"
Link courtesy Google - ↑ Borisov, V.A.; D’yachenko, A.N; Kraidenko, R.I. (2011) "Reaction of Ammonium Chloride with the Copper(II) Sulfide and Oxide, and Identification of the Reaction Products"
Russian Journal of General Chemistry 81(7); pp1430–1433.
DOI:10.1134/S107036321107005X
link courtesy researchgate.