COLLOIDS

Definition
The word colloid comes from a Greek word 'kolla', which means glue, thus colloidal particles
are glue like substances.
A colloid is a substance microscopically dispersed throughout another substance.
These particles pass through a filter paper but not through a semipermeable membrane.
Colloids include gels, sols, and emulsions; the particles do not settle, and cannot be separated out
by ordinary filtering or centrifuging like those in a suspension.
Colloidal System
Colloidal system is made of two phases. The substance distributed as the colloidal particles is
called the Dispersed phase. The second continuous phase in which the colloidal particles are
dispersed is called the Dispersion medium. For example, for a colloidal solution of copper in
water, copper particles constitute the dispersed phase and water the dispersion medium.
The dispersed-phase particles have a diameter of between approximately 1nm – 1000 nm. Such
particles are normally invisible in an optical, though their presence can be confirmed with the
use of an ultra microscope or an electron microscope.
The colloidal solutions or colloidal dispersions are intermediate between true solutions and
suspensions. In other words, the diameter of the dispersed particles in a colloidal dispersion is
more than that of the solute particles in a true solution and smaller than that of a suspension.
When the diameter of the particles of a substance dispersed in a solvent ranges from about 1 nm
to 1000 nm, the system is termed a colloidal solution, colloidal dispersion, or simply a colloid.
The material with particle size in the colloidal range is said to be in the colloidal state.

Homogenous mixtures with a dispersed phase in this size range may be called colloidal aerosols,
colloidal emulsions, colloidal foams, colloidal dispersions, or hydrosols.
If the dispersed phase is solid and the dispersion medium is liquid then it is called colloidal
suspension but if the dispersed phase and dispersion medium both are in liquid state then it is
known as colloidal emulsion.
Examples of colloids: Silver preparation, milk, blood and synthetic polymers, etc.
Comparison of properties of Solutions, Colloids and suspensions
Property True solution Colloid suspension

Particle size Less than 1 nm 1-1000 nm More than 1000 nm

Appearance Clear Cloudy Cloudy

Homogeneity Homogeneous Homogeneous or Heterogeneous Heterogeneous

Transparency Transparent Often translucent or opaque Often opaque but can be translucent

Separation Does not separate Can be separated Separates or settles

Filterability Passes through filter Passes through filter paper Particles do not pass through filter
paper

Classification of Colloids
 Based of physical state of dispersed phase and dispersion medium.
 Based on nature of interaction between dispersed phase and dispersion medium.
 Based on molecular size in the dispersed phase.
 Based on appearance of colloids.
 Based on electric charge on dispersion phase
Based of physical state of dispersed phase and dispersion medium
As we know that a colloidal system is made of a dispersed phase and the dispersion medium.
Because either the dispersed phase or the dispersion medium can be a gas, liquid or solid, there
are eight types of colloidal systems possible. A colloidal dispersion of one gas in another is not
possible since the two gases would give a homogeneous molecular mixture.

Type Name Dispersed Dispersion Medium Examples

Phase

Foam gas liquid Azeliac acid Foam

Solid foam gas solid Ortho Matrix

Aerosol liquid gas Ethylchloride Spray

Emulsion liquid liquid Cod-liver oil emulsion, Milk

Solid Emulsion liquid solid Vicks Balm, Butter

Inhaler Solid gas Ventolin Inhaler

Sol solid liquid Colloidal gold

Solid sol solid solid Sulphur Ointment

Based on nature of interaction between dispersed phase and dispersion medium

Lyophilic and lyophobic sols or colloids
Sols are colloidal systems in which a solid is dispersed in a liquid. These are subdivided into:
a) Lyophilic sols or colloids and
b) Lyophobic sols or colloids
Lyophilic sols are those in which the dispersed phase exhibits a definite affinity for the
dispersion medium. The affinity or attraction of the sol particles for the medium, in a lyophilic
sol, is due to hydrogen bonding with water. If the dispersed phase is a protein (as in egg)
hydrogen bonding takes place between water molecules and the amino groups (–NH–, –NH2) of
the protein molecule. In a dispersion of starch in water, hydrogen bonding occurs between water
molecules and the – OH groups of the starch molecule.
Lyophobic sols are those in which the dispersed phase has no attraction for the medium or the
solvent. The examples of lyophobic sols are dispersion of gold, iron (III) hydroxide and sulphur
in water.
Characteristics of Lyophilic and lyophobic sols
These include:
 Ease of preparation
Lyophilic sols can be obtained straightaway by mixing the material (starch, protein) with a
suitable solvent. The giant molecules of the material are of colloidal size and these at once pass
into the colloidal form on account of interaction with the dispersion medium.
Lyophobic sols are not obtained by simply mixing the solid material with the dispersion medium.
 Charge on particles
Particles of a hydrophilic sol may have little or no charge at all.
Particles of a hydrophobic sol carry positive or negative charge which gives them stability.
 Solvation.
Hydrophilic sol particles are generally solvated. That is, they are surrounded by an adsorbed
layer of the dispersion medium which does not permit them to come together and coagulate.
Hydration of gelatin is an example.
There is no solvation of the hydrophobic sol particles for want of interaction with the medium.
 Viscosity
Lyophilic sols are viscous as the particle size increases due to solvation, and the proportion of
free medium decreases. Warm solutions of the dispersed phase on cooling set to form a gel e.g.,
preparation of table jelly.
Viscosity of hydrophobic sol is almost the same as that of the dispersion medium.
Based on nature of interaction between dispersed phase and dispersion medium
Characteristics of Lyophilic and lyophobic sols
 Precipitation
Lyophilic sols are precipitated (or coagulated) only by high concentration of the electrolytes
when the sol particles are dissolved.
Lyophobic sols are precipitated even by low concentration of electrolytes, the protective layer
being absent.
 Reversibility
The dispersed phase of lyophilic sols when separated by coagulation or by evaporation of the
medium, can be reconverted into the colloidal form just on mixing with the dispersion medium.
Therefore this type of sols are designated as Reversible sols.
On the other hand, the lyophobic sols once precipitated cannot be reformed merely by mixing
with dispersion medium. These are, therefore, called Irreversible sols.
 Tyndall effect
On account of relatively small particle size, lyophilic sols do not scatter light and show no
Tyndall effect. Lyophobic sol particles are large enough to exhibit Tyndall effect.
 Migration in electronic field
Lyophilic sol particles (proteins) migrate to anode or cathode, or not at all, when placed in
electric field.
Lyophobic sol particles move either to anode or cathode, according as they carry negative or
positive charge.
Lyophilic Sols Lyophobic Sols
Prepared by direct mixing with dispersion Not prepared by direct mixing with dispersion
medium medium
Little or no charge on particles Particles carry positive or negative charge
Particles generally solvated No solvation of particles
Viscosity higher than dispersion medium; set Viscosity almost same as that of dispersion
to gel medium; do not set to gel
Precipitated by high concentration of Precipitated by high concentration of
electrolytes electrolytes
Reversible Irreversible
Organic Substances like starch, gelatin Inorganic substances like Ag Cl, Fe (OH)3
Do not exhibit Tyndall effect Exhibit Tyndall effect
Particles migrate to anode or cathode; or not Particles migrate to anode or cathode
at all

Based on molecular size in the dispersed phase.

 Multi-molecular Colloids
Individual particles of the dispersed phase consists of aggregates of atoms or small molecules
having diameter less than 10-7cm . The particles are held by weak van der Waal’s forces.
Example; gold sol, sulphur sol
 Macro-molecular Colloids
The particles of dispersed phase are sufficiently large in size enough to be of colloidal solution.
These are called Natural Polymers. Examples are starch, cellulose and proteins.
Based on appearance of colloids
 Sols
When a colloidal solution appears as fluid. The sols are generally named as dispersion medium.
When the dispersion medium is water, the sol is known as hydrosol or aquosol. When the
dispersion medium is alcohol or benzene, it is called alcosol and benzosol respectively.
 Gels
When a colloidal solution appear as solid. The rigidity of gel varies from substance to substance.
Examples: jelly, butter, cheese, curd.
Based on electrical charge on dispersed phase of colloids
 Positive Colloids
When dispersed phase in a colloidal solution carries a positive charge. Examples: Metal
hyroxides like Fe(OH)3, Al(OH)2, methylene blue sol, etc.
 Negative Colloids
When dispersed phase in a colloidal solution carries a negative charge. Examples: Ag sol, Cu sol
Preparation of Colloids
Lyophilic colloids may be prepared by simply warming the solid with the liquid dispersion
medium e.g., starch with water. On the other hand, lyophobic sols have to be prepared by special
methods.
These methods fall into two categories:
(a) Dispersion Methods in which larger macro-sized particles are broken down to colloidal size.
(b) Aggregation Methods in which colloidal size particles are built up by aggregating single ions
or molecules.
Dispersion Methods
1. Mechanical Dispersion using Colloid Mill
In this method, the solid is first ground to coarse particles and then mixed with dispersion
medium to get a suspension
This suspension is then fed into a Colloid mill. The mill consists of two steel plates nearly
touching each other and rotating in opposite directions with high speed. The solid particles are
ground down to colloidal size and are then dispersed in the liquid to give the colloid. ‘Colloidal
graphite’ (a lubricant) and printing inks are made by this method.
2. Bredig’s Arc Method
It is used for preparing hydrosols of metals e.g., silver, gold and platinum. An arc is struck
between the two metal electrodes held close together beneath de-ionized water. The water is kept
cold by immersing the container in ice/water bath and a trace of alkali (KOH) is added. The
intense heat of the spark across the electrodes vaporises some of the metal and the vapour condenses
under water. Thus the atoms of the metal present in the vapour aggregate to form colloidal particles in
water. Since the metal has been ultimately converted into colloid particles (via metal vapour), this method
has been treated as of dispersion.
Non-metal colloids can be made by suspending coarse particles of the substance in the dispersion
medium and striking an arc between iron electrodes.
3. Peptization
Some freshly precipitated ionic solids are dispersed into colloidal solution in water by the
addition of small quantities of electrolytes, particularly those containing a common ion. The
precipitate adsorbs the common ions and electrically charged particles then split from the
precipitate as colloidal particles.
The dispersal of a precipitated material into colloidal solution by the action of an electrolyte in
solution, is termed peptization. The electrolyte used is called a peptizing agent.
Peptization is the reverse of coagulation of a sol.
Silver chloride, Ag+Cl–, can be converted into a sol by adding hydrochloric acid (Cl– being
common ion.)
Ferric hydroxide, Fe(OH)3, yields a sol by adding ferric chloride (Fe3+ being common ion).
Condensation Methods
These methods consists of chemical reactions or change of solvent whereby the atoms or
molecules of the dispersed phase appearing first, coalesce or aggregate to form colloidal
particles. The conditions (temperature, concentration, etc.) used are such as permit the formation
of colloid particles but prevent the particles becoming too large and forming precipitate. The
unwanted ions (spectator ions) present in the sol are removed by dialysis as these ions may
eventually coagulate the colloid. Some of condensation methods are:
1. Change of Physical State
Solutions of substances like mercury and sulphur are prepared by passing their vapours through a
cold water containing a suitable stabilizer such as ammonium salt or citrate.
2. Excessive Cooling
A colloidal solution of ice in an organic solvent like ether or chloroform can be prepared by
freezing a solution of water in the solvent. The molecules of water which can no longer be held
in solution, separately combine to form particles of colloidal size.
3. Exchange of Solvent
Colloidal solution of certain substances such as sulphur, phosphorus which are soluble in alcohol
but insoluble in water can be prepared by pouring their alcoholic solution in excess of water. For
example, alcoholic solution of sulphur on pouring into water gives milky colloidal solution of
sulphur.
4. Chemical Methods
Some chemical reactions used to aggregate smaller particles of atomic or ionic size to form large
particles of colloidal dimensions. Colloids can be prepared by following chemicals methods:
a) Double Decomposition
An arsenic sulphide (As2S3) sol is prepared by passing a slow stream of hydrogen sulphide gas
through a cold solution of arsenious oxide (As2O3). This is continued till the yellow colour of the
colloid attains maximum intensity.
As2O3 + 3H2S ⎯⎯→ As2S3 (sol) + 3H2O
b) Oxidation
A colloid of sulphur is produced by passing hydrogen sulphide into a solution of sulphur dioxide
(oxidizing agent)
2H2S + SO 2 ⎯⎯→ 2H 2 O + S↓
It can be removed by boiling (to coagulate the sulphur) and filtering through two filter papers
folded together.
c) Reduction
Silver sols and gold sols can be obtained by treating dilute solutions of silver nitrate or gold
chloride with organic reducing agents like tannic acid or methanol (HCHO)
AgNO 3 + tannic acid ⎯⎯→ Ag sol
AuCl 3 + tannic acid ⎯⎯→ Au sol
d) Hydrolysis
Sols of the hydroxides of iron, chromium and aluminium are readily prepared by the hydrolysis
of salts of the respective metals. In order to obtain a red sol of ferric hydroxide, a few drops of
30% ferric chloride solution is added to a large volume of almost boiling water and stirred with a
glass rod.
FeCl3 + 3H2 O ⎯⎯→ Fe(OH)3 + 3HCl
red sol
Purification of Colloidal Solutions
The colloids prepared by above methods frequently contain beside colloidal particles appreciable
amounts of electrolytes. To obtain the pure sol, these electrolytes have to be removed. This
purification of colloids can be accomplished by the following methods:
a) Dialysis
b) Electrodialysis
c) Ultrafiltration
Dialysis
Animal membranes (bladder) or those made of parchment paper and cellophane sheet, have very
fine pores. These pores permit ions (or small molecules) to pass through but not the large
colloidal particles. When a sol containing dissolved ions (electrolyte) or molecules is placed in a
bag of permeable membrane dipping in pure water, the ions diffuse through the membrane. By
using a continuous flow of fresh water, the concentration of the electrolyte outside the membrane tends
to be zero. Thus diffusion of the ions into pure water remains brisk all the time. In this way, practically all
the electrolyte present in the sol can be removed easily.
The process of removing ions (or molecules) from a sol by diffusion through a permeable
membrane is called Dialysis. The apparatus used for dialysis is called a Dialyser.

Electrodialysis
In this process, dialysis is carried under the influence of electric field. Potential is applied
between the metal screens supporting the membranes. This speeds up the migration of ions to the
opposite electrode. Hence dialysis is greatly accelerated. Evidently, electrodialysis is not meant
for nonelectrolyte impurities like sugar and urea.
Ultrafiltration
Sols pass through an ordinary filter paper, Its pores are too large to retain the colloidal particles.
However, if the filter paper is impregnated with collodion or a regenerated cellulose such as
cellophane, the pore size is much reduced. Such a modified filter paper is called an ultrafilter.
The separation of the sol particles from the liquid medium and electrolytes by filtration through
an ultrafilter is called ultrafiltration.
Ultrafiltration is a slow process. Gas pressure has to be applied to speed it up. The colloidal
particles are left on the ultrafilter in the form of slime. The slime may be stirred into fresh
medium to get back the pure sol. By using graded ultrafilters, the technique of ultrafiltration can
be employed to separate sol particles of different sizes.

Properties of Colloids
a) Physical Properties
 Heterogeneity: Colloidal solutions consist of two phases-dispersed phase and dispersion
medium.
 Visibility of dispersed particles: The dispersed particles present in them are not visible
to the naked eye and they appear homogenous.
 Filterability: The colloidal particles pass through an ordinary filter paper. However, they
can be retained by animal membranes, cellophane membrane and ultrafilters.
 Stability: Lyophilic sols in general and lyophobic sols in the absence of substantial
concentrations of electrolytes are quite stable.
 Color: The color of a colloidal solution depends upon the size of colloidal particles
present in it. Larger particles absorb the light of longer wavelength and therefore transmit
light of shorter wavelength.

b) Optical Properties
When a strong beam of light is passed through a sol and viewed at right angles, the path of light
shows up as a hazy beam or cone. This is due to the fact that sol particles absorb light energy and
then emit it in all directions in space. This ‘scattering of light’, as it is called, illuminates the path
of the beam in the colloidal dispersion. The phenomenon of the scattering of light by the sol
particles is called Tyndall effect.
The illuminated beam or cone formed by the scattering of light by the sol particles is often
referred as Tyndall beam or Tyndall cone. True solutions do not show Tyndall effect. Since ions
or solute molecules are too small to scatter light, the beam of light passing through a true
solution is not visible when viewed from the side. Thus Tyndall effect can be used to distinguish
a colloidal solution from a true solution.

c) Kinetic Properties (Brownian movement)

When a sol is examined with an ultramicroscope, the suspended particles are seen as shining
specks of light. By following an individual particle it is observed that the particle is undergoing a
constant rapid motion. It moves in a series of short straight-line paths in the medium, changing
directions abruptly.
The continuous rapid zig-zag movement executed by a colloidal particle in the dispersion
medium is called Brownian movement or motion. Suspensions and true solutions do not exhibit
Brownian movement.
According to kinetic molecular theory, at any instant a colloidal particle was being struck by
several molecules of the dispersion medium. The movement of the particle was caused by
unequal number of molecules of the medium striking it from opposite directions. When more
molecules struck the particle on one side than on another, the direction of movement changed.
The phenomenon of Brownian movement is an excellent proof of the existence of molecules and
their ceaseless motion in liquids. It also explains how the action of gravity, which would
ordinarily cause the settling of colloidal particles, is counteracted. The constant pushing of the
particles by the molecules of the dispersion medium has a stirring effect which does not permit
the particles to settle.
4) Electrical Properties
a) Colloid particles carry an electric charge
The most important property of colloidal dispersions is that all the suspended particles possess
either a positive or a negative charge. The mutual forces of repulsion between similarly charged
particles prevent them from aggregating and settling under the action of gravity. This gives
stability to the sol.
The sol particles acquire positive or negative charge by preferential adsorption of positive or
negative ions from the dispersion medium. For example, a ferric hydroxide sol particles are
positively charged because these adsorb Fe+3 ions from ferric chloride (FeCl3) used in the
preparation of the sol. Since the sol as a whole is neutral, the charge on the particle is
counterbalanced by oppositely charged ions termed counterions (in this case Cl-) furnished by
the electrolyte in medium.
Electrical Double Layer
The surface of colloidal particle acquires a positive charge by selective adsorption of a layer of
positive ions around it. This layer attracts counterions from the medium which form a second
layer of negative charges. The combination of the two layer of + Ve and – Ve charges around the
sol particle was called Helmholtz Double layer. He thought that positive charges next to the
particle surface are fixed, while the layer of negative charges along with the medium are mobile.
This layer is composed of
a) Compact layer of positive and negative charges which are fixed firmly on the particle surface.
b) a Diffuse layer of counterions (negative ions) diffused into the medium containing positive
ions.
The combination of the compact and diffuse layer is referred to as the Stern Double layer after
the colloid chemist who first realized its significance. The diffuse layer is only loosely attached to
the particle surface and moves in the opposite direction under an applied electric field. Because of the
distribution of the charge around the particle, there is a difference in potential between the compact layer
and the bulk of solution across the diffuse layer. This is called by Electrokinetic or Zeta potential. The
presence of the double layer accounts for the electrical properties of colloids.
b) Electrophoresis
If electric potential is applied across two platinum electrodes dipping in a hydrophilic sol, the
dispersed particles move toward one or the other electrode. The movement of sol particles under
an applied electric potential is called electrophoresis or cataphoresis.
If the sol particles migrate toward the positive electrode, they carry a negative charge. On the
other hand, if they move toward the negative electrode, they are positively charged. Thus by
noting the direction of movement of the sol particles, we can determine whether they carry a positive
or negative charge.
The phenomenon of electrophoresis can be demonstrated by placing a layer of As2S3 sol under
two limbs of a U-tube. When a potential difference of about 100 volts is applied across the two
platinum electrodes dipping in deionised water, it is observed that the level of the sol drops on
the negative electrode side and rises on the positive electrode side. This shows that As2S3 sol has
migrated to the positive electrode, indicating that the particles are negatively charged. Similarly, a
sol of ferric hydroxide will move to the negative electrode, showing that its particles carry
positive charge.

c) Electro-osmosis
A sol is electrically neutral. Therefore the dispersion medium carries an equal but opposite charge to
that of the dispersed particles. Thus the medium will move in opposite direction to the dispersed phase
under the influence of applied electric potential. When the dispersed phase is kept, stationary, the
medium is actually found to move to the electrode of opposite sign that its own. The movement of the
dispersion medium under the influence of applied potential is known as electro osmosis.
Electro-osmosis is a direct consequence of the existence of zeta potential between the sol particles and
the medium. When the applied pressure exceeds the zeta potential, that diffuse layer moves and causes
electro-osmosis. The phenomenon of electro-osmosis can be demonstrated by using a U-tube in which a
plug of wet clay (a negative colloid) is fixed. The two limbs of the tube are filled with water to the same
level. The platinum electrodes are immersed in water and potential applied across them. It will be
observed that water level rises on the cathode side and falls on anode side. This movement of the
medium towards the negative electrode, shows that the charge on the medium is positive. Similarly, for
a positively charged colloid electro-osmosis will take place in the reverse direction.
d) Coagulation or precipitation
Lyophobic colloids are stable due to adsorption of positive or negative ions by the dispersed particles.
The repulsive forces between the charged particles do not allow them to settle. If, some how, the charge
is removed, there is nothing to keep the particles apart from each other. They aggregate (or flocculate)
and settle down under the action of gravity. The flocculation and settling down of the discharged sol
particles is called coagulation or precipitation of the sol.
Coagulation of a given sol can be brought about by a) by addition of electrolytes b) by electrophoresis c)
by mixing two oppositely charged sols and d) by boiling.
By addition of Electrolyte
When excess of an electrolyte is added to a sol, the dispersed particles are precipitated. The electrolyte
furnishes both positive and negative ions in the medium. The sol particles adsorb the oppositely charged
ions and get discharged. The electrically neutral particles then aggregate and settle down as precipitate.
A negative ion (anion) causes the precipitation of a positively charged sol, and vice versa. The
effectiveness of an anion or cation to precipitate a sol, will naturally depend on the magnitude of the
charge or valence of the effective ion.
The precipitation power of an electrolyte or ion is experimentally determined by finding the minimum
concentration in millimoles per liter required to cause the precipitation of a sol in 2 hours. This is called
the Flocculation value. The smaller the flocculation value the higher the precipitating power of an ion.
By Electrophoresis
In electrophoresis the charged sol particles migrate to the electrode of opposite sign. As they come in
contact with the electrode, the particles are discharged and precipitated.
By mixing two oppositely charged sols
The mutual coagulation of two sols of opposite charge can be effected by mixing them. The positive
particles of one sol are attracted by the negative particles of the second sol. This is followed by mutual
adsorption and precipitation of both the sols. Ferric hydroxide (+ Ve sol) and arsenious sulphide (– Ve
sol) form such a pair.
By boiling
Sols such as sulphur and silver halides dispersed in water, may be coagulated by boiling. Increased
collisions between the sol particles and water molecules remove the adsorbed electrolyte. This takes away
the charge from the particles which settle down.
e) Protective action of colloids
Lyophobic sols are readily precipitated by small amounts of electrolytes. However these sols are often
stabilized by the addition of lyophilic sols. The property of lyophilic sols to prevent the precipitation of a
lyophobic sol is called protection. The lyophilic sol used to protect a lyophobic sol from precipitation is
referred to as a Protective colloid.
Example: If a little gelatin (hydrophilic colloid) is added to a gold sol (hydrophobic sol), the latter is
protected. The ‘protected gold sol’ is no longer precipitated on the addition of sodium chloride.
Explanation: The particles of the hydrophobic sol adsorb the particles of the lyophilic sol. Thus the
lyophilic colloid forms a coating around the lyophobic sol particles. The hydrophobic colloid, therefore,
behaves as a hydrophilic sol and is precipitated less easily by electrolytes.
The lyophilic colloids differ widely in their powers of protection. The protective action of different
colloids is measured in terms of the ‘Gold number’ introduced by Zsigmondy. The gold number is
defined as: the number of milligrams of a hydrophilic colloid that will just prevent the precipitation of 10
ml of a gold sol on the addition of 1 ml of 10 per cent sodium chloride solution.
The onset of precipitation of the gold sol is indicated by a color change from red to blue when the particle
size just increases. The smaller the gold number of a hydrophilic colloid, the greater is its protective
power. Gelatin has a small gold number and is an effective protective colloid. Starch has a very high
value, which shows that it is an ineffective protective colloid.
The use of protective colloids to stabilize colloidal systems is widespread. In the preparation of ice cream,
gelatin is added to act as a protecting agent to the colloidal particles of ice. If the ice particles coagulate,
the smooth texture of ice cream is lost.
Origin of charge on colloid particles
All the dispersed particles of a particular sol carry a positive or a negative charge. They acquire this
charge by: a) Adsorption of ions from the aqueous medium and b) Ionisation of surface groups.
- Adsorption of ions:
In most cases the charge on the sol particles originates by the selective adsorption of ions common to the
particles from the dispersion medium.
Examples. (i) Ferric hydroxide sol particles are positive because they adsorb the common ion Fe3+ from
the aqueous medium.
Fe(OH)3 + Fe+3 ⎯⎯→ Fe(OH)3/ Fe+3
Positive ferric hydroxide sol particle

(ii) Arsenic sulphide sol particles acquire a negative charge since they adsorb the common ion S-2 from
the medium.
As2 S3 + S-2 ⎯⎯→ As2S3/ S-2
Negative arsenic sulphide sol particle
It is not necessary that a particular sol particles always adsorb the same kind of ions. In fact, the particles
may adsorb the anions or cations whichever are in excess and acquire the corresponding charge. For
example, AgCl sol produced by the addition of AgNO3 solution to sodium chloride solution, bears a
positive charge if Ag+ ions are in excess. On the other hand, if Cl-2 ions are in excess, the AgCl sol
particles acquire a negative charge.
- Ionization of surface groups:
(a) Charge on Soaps and Detergent sols: Soaps and detergent sol particles are aggregates of many
molecules. The hydrocarbons tails of the molecules are directed to the center, while the groups – COO-
Na+ (or – OS O3- Na+ ) constitute the surface in contact with water. As a result of ionization of the surface
groups, the particle surface is now made of the anionic heads – COO- (or – OS O3- ). This makes the sol
particle negative.
(b) Charge on Protein sols. Protein sol particles possess both acidic and basic functional groups. In
aqueous solution at low pH, the –NH2 group (basic) acquires a proton to give –NH3+ while at high pH
the —COOH group (acidic) transfers a proton to OH– to give —COO–. Thus the protein sol particle has
positive charge at low pH and negative charge at high pH. At an intermediate pH called the isoelectric
point, the particles will be electrically neutral. The changes in the charge of the protein sol are shown by
the direction of movement of the dispersed phase in electrophoresis.

Stability of colloids
A true colloidal solution is stable. Its particles do not ever coalesce and separate out. The stability of sols
is mainly due to two factors:
a) Presence of like charges on sol particles
The dispersed particles of a hydrophobic sol possess a like electrical charge (all positive or all negative)
on their surface. Since like charges repel one another, the particles push away from one another and resist
joining together. However, when an electrolyte is added to a hydrophobic sol, the particles are discharged
and precipitated.
b) Presence of solvent layer around sol particles
The lyophilic sols are stable for two reasons. Their particles possess a charge and in addition have a layer
of the solvent bound on the surface. For example, a sol particle of gelatin has a negative charge and a
water layer envelopes it. When sodium chloride is added to colloidal solution of gelatin, its particles are
not precipitated. The water layer around the gelatin particle does not allow the Na+ ions to penetrate it
and discharge the particle. The gelatin sol is not precipitated by addition of sodium chloride solution.
Evidently, lyophilic sols are more stable than lyophobic sols.
Pharmaceutical Applications of colloids
1. Colloidal material are used for a variety of pharmaceutical application including therapeutic &
diagnostic agents, drug delivery system.
Example: copper colloids (anticancer) and mercury colloids (anti syphilis).
2. Drug substances may also be prepared as colloidal sized particles to improve bioavailability or
therapeutic activity.
Example: colloidal Sulphur, etc.
3. Colloidal dispersion of gelatin is used in coating over tablets & granules which upon drying leaves
uniformly dry film over them & protect them from adverse condition of the atmosphere.
4. Most of the medicines are colloidal such as Calcium & Gold are administered by injections to raise the
vitality of human system.
5. Colloidal dispersion containing radioactive isotopes are being used as diagnostic & therapeutic agents
in nuclear medicines.
Sample Questions-Colloids
SEQs
1. What are colloids? How are they classified?
2.
(a) What is meant by peptization? Give a suitable example.
(b) Describe a method for purifying colloidal solutions.
(c) Discuss the function of a protective colloid.
3. What are lyophillic colloids? Why are they called reversible colloids?
4. Discuss the origin of charge on colloidal particles. What is meant by electrical double layers? What is
meant by Zeta potential?
5. Explain the stability of colloids.
6. State different methods of preparation of colloidal dispersions. Describe Bredig’s arc method in detail.
7.
(a) What is a colloid? Discuss the essential difference between lyophilic and lyophobic colloids.
(b) Write short notes on:
(i) Tyndall effect and Brownian movement
(ii) Electrophoresis and its applications
8.
(a) What is a protective colloid? How does a hydrophilic colloid stabilise a hydrophobic one? Give an
account of Gold number in this context.
(b) What do you understand by the coagulation value of an electrolyte?
9. Give in details the methods of preparation of colloids.
10. What is electrophoresis? How does this phenomenon provide information about the sign of charge on
particles?
11. Explain Shulz Hardy Rule for coagulation
12. Describe one methods of preparation of colloidal solutions
13. Give three points of difference between lyophobic and lyophilic colloids
14. (a) What is the size range of colloidal particles? Distinguish between a molecular solution and a
colloidal dispersion.
(b) Describe one method for the preparation of colloidal solutions.
15. Write a short note on ‘origin of charge on colloidal particles’.
16. Give in details the methods of preparation of colloids.
17. Give three points of difference between lyophobic and lyophilic colloids.
18. Define gold number. The gold numbers of A, B, C and D are 0.005, 0.05, 0.5 and 5 respectively.
Which of these has the greatest protective action. Explain your answer.

MCQs
1. In true solutions, the diameter of the dispersed particles is in the range from
(a) 1 Å to 10 Å (b) 10 Å to 100 Å (c) 100 Å to 200 Å (d) 200 Å to 500 Å
2. A colloidal solution consists of
(a) a dispersed phase (b) a dispersion medium (c) a dispersed phase in a dispersion medium (d) a
dispersion medium in a dispersed phase
3. The sols in which the dispersed phase exhibits a definite affinity for the medium or the solvent is
called
(a) lyophillic sols (b) lyophobic sols (c) emulsions (d) hydrosols
6. The scattering of light by the dispersed phase is called
(a) Brownian movement (b) Tyndall effect (c) adsorption (d) electrophoresis
7. In lyophobic sols, the dispersed phase has no _______ for the medium or solvent
(a) repulsion (b) attraction (c) solvation (d) hydration
8. The lyophillic sols are
(a) reversible in nature (b) irreversible in nature
(c) sometimes reversible sometimes nonreversible (d) none of the above
9. The dispersal of a precipitated material into colloidal solution by the action of an electrolyte in solution
is called
(a) coagulation (b) dialysis (c) peptization (d) ultra-filtration
10. An arsenic sulphide sol (AS2S3) is prepared by the reaction
AS2O3 + H2S → AS2S3(sol) + 3H2O
This method of preparing colloidal solution is
(a) reduction (b) oxidation (c) hydrolysis (d) double decomposition
11. A sol of sulphur is produced by passing hydrogen sulphide into solution of sulphur dioxide
2H2S + SO2 → 2H2O + S
This method is known as
(a) reduction (b) oxidation (c) hydrolysis (d) double decomposition
12. The process of removing ions (or molecules) from a sol by diffusion through a permeable membrane
is called
(a) ultra-filtration (b) dialysis (c) electrophoresis (d) osmosis
13. _______ do not show Tyndall effect
(a) true solution (b) colloidal solutions (c) suspensions (d) none of these
14. The continuous rapid zig-zag movement executed by a colloidal particle in the dispersion medium is
called
(a) Tyndall effect (b) Brownian movement (c) electrophoresis (d) peptization
15. The movement of sol particles under an applied electric potential is called
(a) electrophoresis (b) electro-osmosis (c) electrofiltration (d) none of these
16. The presence of the double layer in colloids accounts for
(a) kinetic properties (b) electrical properties (c) optical properties (d) stability of colloids
17. If the sol particles in a given colloid moves towards the anode, they carry
(a) positive charge (b) negative charge (c) no charge (d) sometimes positive sometimes negative charge
18. The movement of the dispersion medium under the influence of applied potential is known as
(a) osmosis (b) diffusion (c) electro-osmosis (d) electrophoresis
19. The flocculation and settling down of the discharged sol particles is called
(a) peptization (b) coagulation (c) osmosis (d) diffusion
20. The precipitating effect of an ion on dispersed phase increases with the valence of the precipitating
ions. This rule is known as
(a) flocculation value rule (b) Hardy-Schulze rule (c) Brownian rule (d) gold number rule
21. The charge on AS2S3 sol is due to
(a) absorption of H+ ions (b) adsorption of H+ ions (c) adsorption of S2– ions (d) absorption of S2– ions
22. The number of milligrams of a hydrophilic colloid that will just prevent the precipitation of 10 ml of
gold sol on addition of 1 ml of 10 per cent sodium chloride solution is called
(a) gold number (b) charge number (c) absorption number (d) silver number
23. The _______ the gold number of a hydrophilic colloid, the greater is its protective power
(a) higher (b) lower (c) constant (d) none of these
24. Which of the following has minimum flocculating power? Pb4+, Al3+, Ba2+, Na+
(a) Na+ (b) Ba2+ (c) Al3+ (d) Pb4+
25. A sol of Ferric chloride moves to the negative electrode. The colloidal particles carry
(a) no charge (b) positive charge (c) negative charge (d) none of these
26. The precipitating power of Al3+, Na+, Ba2+ is in the order
(a) Na+ > Ba2+ > Al3+ (b) Ba2+ > Na+ > Al3+ (c) Al3+ > Na+ > Ba2+ (d) Al3+ > Ba2+ > Na+
27. An emulsion is a colloidal solution of a _______ dispersed in another liquid
(a) solid (b) liquid (c) gas (d) medium
28. A gel is a colloidal system in which a _______ is dispersed in a _______ medium.
(a) solid, liquid (b) liquid, solid (c) liquid, liquid (d) liquid, gas
29. The human kidneys purify the blood by _______ through natural membranes
(a) osmosis (b) diffusion (c) dialysis (d) emulsification
30. The blue colour of the sky is due to
(a) Brownian movement (b) Tyndall effect (c) the presence of macromolecules (d) electrophoresis