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Welcome To
Chemistry
Done by Aadil
INTRODUCTION
 We know that metals are highly reactive. Therefore, they do
not occur in the free state. For example, sodium, potassium,
etc. are never found in the free state and occur in nature in
chemically combined forms known as minerals.
Elements or compounds, which occur naturally in the Earth’s
crust, are known as minerals. Most minerals found in the
earth’s crust contain metals. Some metals are also found in
the oceans in the form of salts such as sodium chloride,
magnesium chloride, etc.
There are some minerals which contain a large amount of a
particular metal and from them, metals can be extracted
profitably (using practically possible techniques).
GROUP OF METAL BASED ON
REACTIVITY SERIES
 1.Metals of low reactivity
The metals at the bottom of the reactivity series are less
reactive and they often exist in nature in the free state. For
example, gold, silver, and platinum are less reactive metals.
2.Metals of medium reactivity
The metals at the top of the reactivity series are very reactive.
Hence, they never occur in nature in the free state. For
example, sodium, potassium, calcium, etc. are highly reactive,
but do not occur in nature in the free state.
3.Metals of high reactivity
The metals in the middle of the reactivity series are
moderately reactive. For example, zinc, iron, and lead are
moderately reactive.
 Now, let us study how these metals are extracted. A number of steps
are involved in the extraction of metals. They can be summarized in
the form of a figure as follows.
EXTRACTING METALS IN THE MIDDLE OF THE
REACTIVITY SERIES
 Metals that are present in the middle of the reactivity series
such as zinc, iron, lead, and manganese are quite reactive
and exist in nature as oxides, sulphides, and carbonates.
These metals are extracted from their ores by first converting
ores to oxides and then by the reduction of these oxides,
mostly using carbon.
There are two methods by which ores are converted into their
respective oxides: Roasting Calcination
Roasting: It is used to convert sulphide ores into oxides.
Roasting involves strong heating of iron ore in the presence of
excess air. For example, copper sulphide in copper glance ore
is converted into copper (I) oxide by heating it in the presence
of oxygen.
 Calcination: It is used to convert carbonate ores into oxides.
Calcination involves strong heating of the ore in the absence
of air. For example, calamine ore, which is chemically zinc
carbonate, is converted into zinc oxide by heating it in the
absence of air.
After obtaining metal oxides from the ores, reduction of these
metal oxides is done to obtain pure metals. Mostly, carbon in the
form of coke is used for this.
However, the oxides of metals, which are present relatively
higher in the reactivity series such as manganese, cannot be
reduced with coke. To reduce these oxides of metals, more
reactive metals than manganese such as sodium, calcium, and
aluminium are used. For example, iron is also a very reactive
metal and cannot be reduced using carbon.
 Hence, it is reduced using aluminium metal. The reaction is
highly exothermic. The heat evolved is so large that the
metals are produced in the molten form. This reaction is
known as thermit reaction and is used to join railway tracks or
cracked machine parts.
Similarly, manganese cannot be reduced using carbon. Hence,
it is also reduced by aluminium metal.
EXTRACTING METALS TOWARDS
THE TOP OF ACTIVITY SERIES
 Metals present at the top of the series such as sodium,
potassium, calcium, manganese, and aluminium are very
reactive. These metals cannot be reduced using coke as
their affinity for oxygen is much more than that of carbon.
Therefore, these metals are reduced by passing an
electric current through their molten salts. This process
is known as electrolytic reduction.
 For example, sodium metal is extracted from sodium
chloride. To extract the metal, electrolytic reduction of
molten sodium chloride is carried out. When an electric
current is passed, sodium ions which have positive
charge move towards the cathode and get deposited
over it after accepting electrons. The chloride ions have
negative charge and move towards the anode, lose their
extra electrons, and escape out of the solution as
chlorine gas.
 Reaction at cathode (negative electrode):
Reaction at anode (positive electrode):
REFINING OF METALS
 Do you know that the metals obtained by various
reduction processes, except electrolytic reduction,
contain many impurities and require purification? How
are these metals purified?
The method that is most commonly used to purify metals is
electrolytic refining. Many metals such as copper, zinc,
gold, etc. are refined electrolytic ally.
In this process the impure metal is made anode and a thin
strip of pure metal made the cathode. Metal salt is used
as a solution. On passing the current the pure metal from
the anode dissolves in the solution. An equivalent amount
of pure metal from the solution is deposited on cathode.
The soluble impurities go in to the solution while insoluble
impurities settle at the bottom as anode mud.
Metals and Ores, including reactivity seies

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Metals and Ores, including reactivity seies

  • 2. INTRODUCTION  We know that metals are highly reactive. Therefore, they do not occur in the free state. For example, sodium, potassium, etc. are never found in the free state and occur in nature in chemically combined forms known as minerals. Elements or compounds, which occur naturally in the Earth’s crust, are known as minerals. Most minerals found in the earth’s crust contain metals. Some metals are also found in the oceans in the form of salts such as sodium chloride, magnesium chloride, etc. There are some minerals which contain a large amount of a particular metal and from them, metals can be extracted profitably (using practically possible techniques).
  • 3. GROUP OF METAL BASED ON REACTIVITY SERIES  1.Metals of low reactivity The metals at the bottom of the reactivity series are less reactive and they often exist in nature in the free state. For example, gold, silver, and platinum are less reactive metals. 2.Metals of medium reactivity The metals at the top of the reactivity series are very reactive. Hence, they never occur in nature in the free state. For example, sodium, potassium, calcium, etc. are highly reactive, but do not occur in nature in the free state. 3.Metals of high reactivity The metals in the middle of the reactivity series are moderately reactive. For example, zinc, iron, and lead are moderately reactive.
  • 4.  Now, let us study how these metals are extracted. A number of steps are involved in the extraction of metals. They can be summarized in the form of a figure as follows.
  • 5. EXTRACTING METALS IN THE MIDDLE OF THE REACTIVITY SERIES  Metals that are present in the middle of the reactivity series such as zinc, iron, lead, and manganese are quite reactive and exist in nature as oxides, sulphides, and carbonates. These metals are extracted from their ores by first converting ores to oxides and then by the reduction of these oxides, mostly using carbon. There are two methods by which ores are converted into their respective oxides: Roasting Calcination Roasting: It is used to convert sulphide ores into oxides. Roasting involves strong heating of iron ore in the presence of excess air. For example, copper sulphide in copper glance ore is converted into copper (I) oxide by heating it in the presence of oxygen.
  • 6.  Calcination: It is used to convert carbonate ores into oxides. Calcination involves strong heating of the ore in the absence of air. For example, calamine ore, which is chemically zinc carbonate, is converted into zinc oxide by heating it in the absence of air. After obtaining metal oxides from the ores, reduction of these metal oxides is done to obtain pure metals. Mostly, carbon in the form of coke is used for this. However, the oxides of metals, which are present relatively higher in the reactivity series such as manganese, cannot be reduced with coke. To reduce these oxides of metals, more reactive metals than manganese such as sodium, calcium, and aluminium are used. For example, iron is also a very reactive metal and cannot be reduced using carbon.
  • 7.  Hence, it is reduced using aluminium metal. The reaction is highly exothermic. The heat evolved is so large that the metals are produced in the molten form. This reaction is known as thermit reaction and is used to join railway tracks or cracked machine parts. Similarly, manganese cannot be reduced using carbon. Hence, it is also reduced by aluminium metal.
  • 8. EXTRACTING METALS TOWARDS THE TOP OF ACTIVITY SERIES  Metals present at the top of the series such as sodium, potassium, calcium, manganese, and aluminium are very reactive. These metals cannot be reduced using coke as their affinity for oxygen is much more than that of carbon. Therefore, these metals are reduced by passing an electric current through their molten salts. This process is known as electrolytic reduction.
  • 9.  For example, sodium metal is extracted from sodium chloride. To extract the metal, electrolytic reduction of molten sodium chloride is carried out. When an electric current is passed, sodium ions which have positive charge move towards the cathode and get deposited over it after accepting electrons. The chloride ions have negative charge and move towards the anode, lose their extra electrons, and escape out of the solution as chlorine gas.  Reaction at cathode (negative electrode): Reaction at anode (positive electrode):
  • 10. REFINING OF METALS  Do you know that the metals obtained by various reduction processes, except electrolytic reduction, contain many impurities and require purification? How are these metals purified? The method that is most commonly used to purify metals is electrolytic refining. Many metals such as copper, zinc, gold, etc. are refined electrolytic ally. In this process the impure metal is made anode and a thin strip of pure metal made the cathode. Metal salt is used as a solution. On passing the current the pure metal from the anode dissolves in the solution. An equivalent amount of pure metal from the solution is deposited on cathode. The soluble impurities go in to the solution while insoluble impurities settle at the bottom as anode mud.