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Which is not the characteristic of hydro...

Which is not the characteristic of hydrophobic sols?
a. They are highly susceptible to coagulation by addition of electrolytes.
b. They have nearly the same surface tension and viscosity as that of dispersion medium.
c. Their stability is due to both electric charge and salvation of the particles.
d. Sol particles can be seen under ultramicroscope.

A

They are highly susceptible to coagulation by addition of electrolytes

B

They have nearly the same surface tension and viscosity as that of dispersion medium

C

Their stability is due to both the electric charge and solvation of the particles

D

Sol particles can be seen under ultramicroscope

Text Solution

Verified by Experts

The stability is attributed to electric charge on the sol particles.
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Which of the following statements are correct ? 1.on the application of an electric direction field, the particles of lyophobic sol may move in either direction or not move at all 2. surface tension of lyophobic sols is similar to that of the dispersion medium. 3. electro-osmosis is the movement of the particles of dispersion medimum under the influence of an electric field. Select the correct answer using codes given below:

The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. Under the influence of an electric field, the particles in a sol migrate towards cathode. The coagulation of the same sol is studied using NaCl, Na_(2)SO_(4) and Na_(3)PO_(4) solutions. Their coagulating values will be in the order :

The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. A gelatin sol at pH less than the isoelectric value is subjected to an electric field. The sol particles migrate toward :

The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. How would you obtain a sol of AgI, the particles of which migrate towards cathode under the electric field?

The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. Which of the following ions would have the minimum coagulating value for sol obtained on peptizing Sn(OH)_(4) by little NaOH solution?

The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. When 9.0 ml of arsenious sulphide sol and 1.0 ml of 1.0 xx 10^(-4) M BaCl_(2) are mixed, turbidity due to precipitation just appears after 2 hours. The effective ion and its coagulating value are respectively :

The colloidal particles are electrically charged as a indicated by their migration towards cathode or anode under the applied electric field. In a particular colloidal system, all particles carry either positive charge or negative charge. The electric charge on colloidal particles orginate in several ways. According to preferential adsorption theory, the freshly obtained precipitate particles adsorb ions from the dispersion medium, which are common to their lattice and acquire the charge of adsorbed ions. For example, For example, freshly obtained Fe(OH)_(3) precipitated is dispersed, by a little FeCl_(3) , into colloidal solution owing to the adsorption of Fe^(3+) ions in preference. Thus sol particles will be positively charged. In some cases the colloidal particles are aggregates of cations or anions having ampiphilic character. When the ions posses hydrophobic part (hydrocarbon end) as well as hydrophilic part (polar end group), they undergo association in aqueous solution to form particles having colloidal size. The formation of such particles, called micelles plays a very important role in the solubilization of water insoluble substances, (hydrocarbon, oils, fats, grease etc.). In micelles, the polar end groups are directed towards water and the hydrocarbon ends into the centre. The charge on sol particles of proteins depends on the pH. At low pH, the basic group of protein molecule is ionized (protonated) and at higher pH (alkaline medium), the acidic group is ionized. At isoelectric pH, characteristic to the protein, both basix and acidic groups are equally ionized. The stability of colloidal solution is attributed largely to the electric charge of the dispersed particles. This charge causes them to be coagulated or precipitated. On addition of small amount of electrolytes, the ions carrying oppiste charge are adsorbed by sol particles resulting in the neutralization of their charge. When the sol particles either with no charge or reduced charge, come closer due to Brownian movement, they coalesce to form bigger particles resulting in their separation from the dispersion medium. This is what is called coagulating or precipitation of the colloidal solution. The coagulating power of the effective ion, which depend on its charge, is expressed in terms of its coagulating value, defined as its minimum concentration (m mol/L) needed to precipitate a given sol. 100 ml each of two sols of AgI, one obtained by adding AgNO_(3) to slight excess of KI and another obtained by adding KI to slight excess of AgNO_(3) , are mixed together. Then :

In a colloidal state, the particle size of he dispersed phase ranges between 10^(3) to 10^(6) pm and the colloidal sol is of heterogeneous nature. Depending upon the ease with which these sols are formed, the colloidal sols are cassified as lyophilic and lyophobic. THe stability of a colloidal sol is due to the presence of charge on the sol particles and the neutralisation of the same is known as coagulation or precipitation. The coagulationg power of the active ions of he electrolytes can be compared with the help of Hardy-Schulze Law. The protecting power of the lyophilic sols can be compared with the help of gold number. Lesser the value of gold number, more will be the protecting power of the lyophilic sol. The areseneous sulphide sol has negative (-) charge. The maximum power to precipitate it is of :

In a colloidal state, the particle size of he dispersed phase ranges between 10^(3) to 10^(6) pm and the colloidal sol is of heterogeneous nature. Depending upon the ease with which these sols are formed, the colloidal sols are cassified as lyophilic and lyophobic. THe stability of a colloidal sol is due to the presence of charge on the sol particles and the neutralisation of the same is known as coagulation or precipitation. The coagulationg power of the active ions of he electrolytes can be compared with the help of Hardy-Schulze Law. The protecting power of the lyophilic sols can be compared with the help of gold number. Lesser the value of gold number, more will be the protecting power of the lyophilic sol. Lyophilic sols are more stable than lyophobic sols because

In a colloidal state, the particle size of he dispersed phase ranges between 10^(3) to 10^(6) pm and the colloidal sol is of heterogeneous nature. Depending upon the ease with which these sols are formed, the colloidal sols are cassified as lyophilic and lyophobic. THe stability of a colloidal sol is due to the presence of charge on the sol particles and the neutralisation of the same is known as coagulation or precipitation. The coagulationg power of the active ions of he electrolytes can be compared with the help of Hardy-Schulze Law. The protecting power of the lyophilic sols can be compared with the help of gold number. Lesser the value of gold number, more will be the protecting power of the lyophilic sol [AgI]I^(-) colloidal sol can be coagulated by the addition of a suitable action. 1 mol of [AgI]I^(-) required mole of AgNO_(3), Pb (NO_(3))_(2) and Fe(NO_(3))_(3) as: