Metals are found in their ores, and in order to get the pure metal
from the ore, you need to find a way to get rid of the impurities
Roasting is a technique used to convert sulphide ores to the metal oxides
e.g. 2ZnS + 3O2------> 2ZnO + 2SO2
The only problem is that it creates SO2 which is a pollutant, however, this can
then be converted to H2SO4 and sold off as a means of higher profits
Extraction of Iron
The iron ore is known as Haematite Fe2O3
The method of extraction is reduction with carbon
The process occurs in a blast furnace
1. Coke (impure carbon) reacts with oxygen to produce CO2
An exothermic reaction so maintains heat in the furnace
2. CO2 produced reacts with more coke to produce
carbon monoxide
This is the reducing agent
C + CO2 ----> 2CO
An endothermic reaction
The CO reduces the haematite to iron
(Fe2 (+3) + 3e- ----> 2Fe (0)) x2
(CO ------> CO2 + 2e-) x3
Overall: 2FeO3 + 3CO -------> 2Fe + 3CO2
The carbon dioxide could be used to make more reducing agent
By reacting with more coke
The iron will sink to the botton of the furnace to be tapped off
Removing Impurities
The main impurity in this is silicon dioxide
This can be removed by adding calcium carbonate
The calcium carbonate will decompose into calcium oxide
The calcium oxide will react with the silicon dioxide to form calcium silicate
This can be used for breeze blocks, tar
CaO + SiO2 -------> CaSiO3
CaCO3-----> CaO + CO2
Haematite could even react with the carbon: Fe2O3 + 3CO ------> 2Fe + 3CO
More reducing agent also produced
Advantages:
Heat is mainatined by the exothermic reaction
Raw materials are fairly cheap
A continous process
Disadvantages:
Releases CO2- contributes to GW
Doesn't produce pure iron
Not really a bad thing because pure iron is brittle
Extraction of aluminium
This is done by electrolysis
It is too reactive to be
reduced by chemical
means
The aluminium ore is called
bauxite and is very common (Al2O3)
Purification
The ore is dissolved in NaOH
Silicon dioxide found as an impurity in the ore will not dissolve
It is filtered off to remove the SiO2
Electrolysis
Both the anode (positively charged) and cathode
(negatively charged) are made of carbon graphite
Cryolite (Na2AlF6) is added to lower
the melting point of the ore from
around 2000 to 700 degrees celcius
At the anode
2O (2-) ------> O2 + 4e-
Oxidation
At the cathode
Al (+3) + 3e- -------> Al
Reduction
Overall: 2Al2O3-----> 4Al + 3O2
Aluminium formed at the cathode will
sink to the bottom and be tapped off
The O2 formed at the anode may react
with the carbon to produce CO2
Advantages:
A continuous process
Pure aluminium formed
Disadvantages:
Expensive because it's energy intensive
Only works for ionic oxides
Extraction of Titanium
Titanium ore: Rutile, TiO2
The ore has many uses on its own
Paints, paper, milk, polymers, sunscreens etc
Titanium uses:
Hip replacements
Properties
Low density
High strength
resistant to corrosion
We can't use carbon as a reducing
agent because it will form titanium
carbide which is very brittle
To avoid this, we need to chlorinate the TiO2 to
form TiCl4. This is done by heating the ore and
chlorine in the presence of coke
TiO2+ 2Cl2 + C------> TiCl4 + 2CO
The Cl2 is reuced and the C is oxidised. However, the Ti has not been changed
We now have TiCl4 which needs to be reduced. I.e.the chloride ion needs to be reduced
Conditions:
550 degrees c
Exothermic reaction so not much heat is needed
An inert atmosphere of argon so the TiCl4
doesnt react with oxygen to form the ore again
TiCl4 is to be vapourised
Reducing agent: Mg or Na
Overall equation:
TiCl4 + 2Mg ------> MgCl2 + Ti
Half eq
Ti (4+) + 4e- ------> Ti (0)
Mg------ Mg (2+) + 2e-
TiCl4 + 4Na -------> Ti + NaCl
Half eq
Ti (4+) + 4e- ------> Ti
Na ------> Na + e-
Sealed container
Advantages: Pure titanium
Exothermic
Disadvantages: Batch Process
Extraction of tungsten
Use: Light bulb filaments
Properties: High density, high temp resistant
Ore: WO3
Reducing agent: H2 gas
Overall Eq:
WO3 + 3H2 ------> W + 3H2O
High temp required
Advantages: Pure tungsten produced
Reducing agent is cheap
Disadvantages: H2 is flammable
Expensive: Energy intensive
Dynamic Equilibria
Dynamic: A reaction that goes forward and backwards
Equilibria: Where the forward and backwards reaction takes place at the same speed
A closed system
The conc of the reactants and products are constant
Where both the forward and backward reactions are taking place at the same rate
The position of equilibria can be shown on a diagram
A catalyst will not affect the position of the equilibria,
all it does is it reduces the time it takes to get to the
equilibrium
This is because it speeds up both the forward and backward reaction
LeChatiliers principle: This is the idea that if change the conditions of an
equilibrium, then the equilirbium system will move to oppose that change.
E.g. if you make it warmer, the
equilibrium will move to make it cooler
Examples:
The haber process:
N2 + 3H2--------> 2NH3 (-92 kJmol-1)
Conditions:
High pressure: You get more
yield as the equilibrium system
will try and oppose the change
and produce more of the side
with fewer partices i.e. more
product
Around 20000kPa
Dangerous
Expensive
Ideally, Lower: Decreasing temp mean system will
try and oppose it and increase the temp by forcing
reaction in the exo direction which id the forward
direction
But then that means a lower rate of reaction
so a compromise of around 380-450 is used
Products tapped off and reactants continuously fed
in, favour forward reaction due to lechatiliers principle
Hydration of Ethene
C2H4 + H2O -------> C2H5OH (-461kJmol-1)
High pressure (6500kPa)
Ideally low temp but a compromise is used
for a high rate of reaction (570 k)
Conc: Compromised: You dont want too much in there because addition
polymerisation takes place and thos blocks the active site of the catalyst
Also, too much water will dilute the catalyst
However, a lower conc means a lower rate of reaction
Production of methanol
CO + 2H2 ------> CH3OH (-91kJmol-1)
High pressure (10000 kPa)
Compromised temp of 500k
Uses: Perspex glasses, bus windows, chemical feedstock