The Nature of the Sol
To master the concept of coagulation, we must first understand the battlefield. Colloidal solutions, or sols, are incredibly stable because the dispersed particles carry an identical electrical charge. This mutual electrostatic repulsion prevents them from coming together and settling down.
In our specific problem, we are dealing with an arsenic sulphide sol (As2S3). A crucial piece of factual knowledge you must carry into the exam is that metal sulphides generally form negatively charged sols. Imagine a central colloidal particle of As2S3 surrounded by a protective, invisible shield of negative charges.
The Weapon of Choice
Coagulation
To destroy this stability—a process called coagulation or precipitation—we need to neutralize that protective negative shield. We do this by introducing an electrolyte, which splits into positive and negative ions. For a negatively charged sol, the active agents are the positive ions (cations), also known as flocculating ions.
The Master Equation
Hardy-Schulze Rule
This brings us to the elegant Hardy-Schulze Rule. It dictates a very simple but powerful principle: the coagulating power of an ion is directly proportional to its valency (or the magnitude of its charge).
Coagulating Power∝Valency of Flocculating Ion
Simply put, an ion with a higher charge is a much more potent weapon for neutralizing the sol than an ion with a lower charge. It can neutralize more colloidal particles per ion, making the process highly efficient.
Final Calculation and Conclusion
Let's inspect the arsenal provided by the electrolytes in the question:
1. Sodium ion: Na+ (Charge = +1)
2. Barium ion: Ba2+ (Charge = +2)
3. Aluminum ion: Al3+ (Charge = +3)
Applying the Hardy-Schulze rule, we simply arrange these ions in increasing order of their positive charge:
Therefore, the increasing order of their coagulating power is:
This perfectly matches option (b). Always remember to first identify the charge of the sol, and then look for the oppositely charged ion with the highest valency!