Friday, May 8, 2020

JEE Advanced 2020 Exam Date announced, to be conducted on August 23, 2020

Joint Entrance Examination, JEE Advanced or IIT JEE Exam dates 2020 have been announced. Union HRD Minister Ramesh Pokhriyal today shared that the JEE Advanced 2020 would be conducted on August 23, 2020. The dates for JEE Main 2020 were announced on May 5 by the HRD Minister during a webinar with the students.
JEE Main 2020 would be conducted from July 18 to July 23. Given the date of the JEE Advanced 2020, it can be suggested that the results of JEE Main 2020 are expected to be announced by August 10. The online application process for JEE Advanced 2020 would begin only after the final results of JEE Main 2020 are announced along with the JEE Main 2020 Ranks.



As many as 2.5 lakh stduents, based on their JEE Main 2020 scores would be eligible to appear for the examination. JEE Advanced 2020 is the entrance/admission test for the top technical institiutes in the country. The announcemnet of the dates would help lakhs of students who are preparing for the entrance examination. 
Students may please note that the timeline provided above is only based on the usual time frame followed by the IITs in regards the examination. The actual schedule would be announced by IIT Delhi in a few days time. IIT JEE or JEE Advanced 2020 is conducted by the IITs while JEE Main, the qualifier is conducted by National Testing Agency. Both JEE Main and JEE Advanced 2020 would be online or computer based tests. 

Source: Times Now News Update

Thursday, April 30, 2020

Electrical Properties of Colloidal Solution

Q1. How you will account for the presence of electrical charge on colloidal particles?
Ans:In a particular colloidal solution, all the colloidal particles carry the same type of charge, while the dispersion medium has an equal but opposite charge. Thus, the charge on colloidal particles is balanced by that of the dispersion medium and the colloidal solution as a whole is electrically neutral.
For example:  In a ferric hydroxide {Fe(OH)3} sol, the colloidal ferric hydroxide particles are positively charged, while the dispersion medium carries an equal and opposite negative charge.

Q2. How is the presence of charge on colloidal particles responsible for the stability of colloidal sols?
Ans: The stability of a colloidal solution is mainly due to the presence a particular type

of charge on all the colloidal present in it. Due to the presence of similar and equal charges, the colloidal particles repel one another and are thus unable to combine together to form larger particles or settle down . This keeps them dispersed in the dispersion medium and the colloidal remains stable. This is why sol particles do not settle down even on standing for a long time.

Q3. Explain the classification of colloidal solution depending upon the nature of charge on the particles of the dispersed phase?
Ans: the colloidal solutions can be classified into positively charged and negatively charged colloids. Some of the typical examples of it are as follows:
                             


# THEORIES OF ORIGIN OF CHARGE ON COLLOIDAL PARTICLES

Q4: How will you account for the origin of Charge on Colloidal Particles?
Ans: There are several views regarding the origin of charge on colloidal particles. According to these views, colloidal particles acquire charge due to the following reasons.
1.Due to dissociation of the adsorbed molecular electrolytes: (i) (i) Colloidal particles have a strong tendency to adsorb reactant or product molecules. The molecules thus adsorbed on the surface of colloidal particles may undergo dissociation/ionization and may impart charge to them.
For example: During the preparation of sulphide sols (e.g., As2S3 sol), H2S molecules get adsorbed on colloidal particles. H2S molecules thus adsorbed undergo ionization and release H+ ions into the medium. Consequently, colloidal particles are left with negative charge.
(ii) Due to the dissociation of molecules forming colloidal aggregates: The molecules responsible for the formation of aggregates of colloidal dimensions may themselves undergo dissociation/ionisation resulting in the development of charge on the colloidal particles formed by their aggregation.
For example: The soap molecules (RCOONa) dissociate to give RCOO- and Na+ ions. RCOO- ions aggregate due to weak attractive forces present in the hydrocarbon chains together to form micelles which carry negative charge as explained earlier.
(2) Due to frictional electrification
(i) It is supposed that the frictional electrification due to the rubbing of the dispersed phase particles with that of dispersion medium results in some charge on the colloidal particles.
(ii) The dispersion medium must also get some charge, due to the friction. As it does not carry any charge, theory does not appear to be correct.
(3) Due to selective adsorption of ions / Due to preferential adsorption of ions from solutions: The colloidal particles have a tendency to preferentially adsorb a particular type of ions from the solution. A colloidal particle usually adsorbs those ions which are in excess and are common to its own lattice.
For example: When a ferric hydroxide sol is prepared by the hydrolysis of ferric chloride in warm water, the colloidal particles of Fe(OH)3 formed have a tendency to adsorb preferentially the Fe3+ ions present in the solution. This is because Fe3+ ions are common to the lattice of Fe(OH)3 particle. The Fe3+ ions thus adsorbed impart positive charge to the colloidal particles present in the sol.

        
   
(ii) For example: When a small quantity of silver nitrate (AgNO3) solution is added to a large quantity of potassium iodide KI solution, colloidal particles of the silver iodide adsorb I- from the solution to become negatively charged, (at this stage KI is in excess, and I-being common to AgI)   
         

But, when a small quantity of potassium iodide (KI) solution is added to a large quantity of silver nitrate solution (AgNO
3); the colloidal silver iodide particles adsorb Ag+ from the solution to become positively charged, (at this stage AgNO3 is in excess and Ag+ is common to AgI),
          

Text Box:
1. Electrophoresis: Due to the presence of a particular type of electrical charge, the colloidal particles present in a colloidal dispersion move towards a particular electrode under the influence of an electric field.
The direction of movement of the colloidal particles is decided by the nature of charge present on them. If the colloidal particles carry positive charge, they move towards cathode when subjected to an electric field and vice versa. The phenomenon is called electrophoresis.
 It  may be defined as “ the movement of colloidal particles towards a particular electrode under the influence of an electric field”.
Electrophoresis is an important phenomenon and finds several applications in industry.
       2. Electro-Osmosis:
It may be defined as the  movement of dispersion medium under the influence of an electric field in the situation when the movement of colloidal particles is prevented with the help of a suitable membrane.
The colloidal solution is placed between two partitions made by semi permeable membranes.The outer compartments consisting of platinum electrodes and side tubes are filled with water. On passing electric current, water level begins to rise in one of the side tubs and falls in the other.
The phenomenon can be explained as follows :
We have already seen that the colloidal particles and dispersion medium carry charges which are equal but opposite in nature. Under the influence of an electric field, both have a tendency to move towards the oppositely charged electrodes. Semi permeable membranes do not allow the passage of colloidal particles. However, dispersion medium can pass through them. Therefore during electro-osmosis, colloidal particles are checked and it is the dispersion medium that moves towards the oppositely charged electrode.

3. Electrokinectic Potential OR Zeta Potential
Having acquired a positive or a negative charge by selective adsorption on the surface of a colloidal particle as stated above, this layer attracts counter ions from the medium forming a second layer, as shown below. AgI/I- K+ AgI/Ag+ I – .
The combination of the two layers of opposite charges around the colloidal particle is called Helmholtz electrical double layer. According to modern views, the first layer of ions is firmly held and is termed fixed layer while the second layer is mobile which is termed diffused layer.
Since separation of charge is a seat of potential, the charges of opposite signs on the fixed and diffused parts of the double layer results in a difference in potential between these layers. This potential difference between the fixed layer and the diffused layer of opposite charges is called the electrokinetic potential or zeta potential.
                         
This potential difference between the fixed layer and the diffused layer of opposite charges is called the electrokinetic potential or zeta potential.

Noted Credit: Mr Pradeep Sharma