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Aye Finance Interview Questions and Answers

Updated 22 Jan 2025
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Q1. Which type packing is batter in distillation continue?

Ans.

The type of packing that is better in distillation depends on the specific application and desired outcome.

  • Structured packing is better for high efficiency and low pressure drop

  • Random packing is better for high capacity and fouling resistance

  • Trays are better for high turndown ratio and easy maintenance

  • Factors to consider include composition of the mixture, desired separation efficiency, pressure drop limitations, and cost

  • Common types of packing include metal, plastic, and cer...read more

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Q2. What is vacuum distillation? How to create vacuum?

Ans.

Vacuum distillation is a process of separating components of a mixture by boiling it under reduced pressure.

  • It is used to separate components with high boiling points.

  • The process involves heating the mixture in a vacuum to lower the boiling point.

  • The lower pressure also reduces the risk of thermal decomposition.

  • Vacuum can be created using a vacuum pump or aspirator.

  • Examples include the separation of crude oil into different fractions and the purification of solvents.

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Q3. What is critical process parameter during granulation.

Ans.

The critical process parameter during granulation is the moisture content of the granules.

  • Moisture content affects the flowability and compressibility of the granules.

  • It also impacts the final product quality and stability.

  • Examples of critical moisture content ranges are 2-4% for wet granulation and 1-3% for dry granulation.

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Q4. What will you do if power interruption during wet granulation.

Ans.

I will immediately stop the wet granulation process, secure the equipment, and address the power interruption before resuming production.

  • Stop the wet granulation process immediately to prevent any damage to the equipment or product

  • Secure the equipment to ensure safety and prevent accidents during the power interruption

  • Address the power interruption by checking the power source, circuit breakers, and contacting maintenance if needed

  • Resume production only after ensuring that th...read more

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Q5. What are yours keys functionality to grow urs organization.

Ans.

Effective communication, strategic planning, talent development, innovation

  • Implementing clear communication channels to ensure all team members are aligned with organizational goals

  • Developing and executing strategic plans to drive growth and achieve objectives

  • Investing in talent development programs to nurture and retain top performers

  • Fostering a culture of innovation to stay ahead of competitors and adapt to market changes

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Q6. Type of distillation?

Ans.

There are various types of distillation methods such as simple distillation, fractional distillation, steam distillation, vacuum distillation, etc.

  • Simple distillation is used to separate liquids with different boiling points

  • Fractional distillation is used to separate liquids with similar boiling points

  • Steam distillation is used to extract essential oils from plants

  • Vacuum distillation is used to distill high boiling point compounds at lower temperatures

  • Other types of distillat...read more

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Q7. Boiling point of solvent

Ans.

The boiling point of a solvent depends on its chemical composition.

  • The boiling point of a solvent is the temperature at which it changes from a liquid to a gas.

  • Solvents with stronger intermolecular forces have higher boiling points.

  • For example, water has a boiling point of 100°C, while acetone has a boiling point of 56°C.

  • The boiling point can also be affected by external factors such as pressure.

  • Knowing the boiling point of a solvent is important for various industrial proces...read more

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Q8. What is gmp explain

Ans.

GMP stands for Good Manufacturing Practice, a set of guidelines ensuring products are consistently produced and controlled according to quality standards.

  • GMP is a system for ensuring that products are consistently produced and controlled according to quality standards.

  • It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.

  • Examples of GMP guidelines include proper sanitation, validation of equi...read more

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