Abstract:
The purification of pharmaceutical compounds plays a crucial role in ensuring the safety and efficacy of drugs. Traditional separation techniques often suffer from limitations such as low selectivity, high energy consumption, and environmental concerns. This research aims to explore and analyze novel separation techniques for the purification of pharmaceutical compounds, with a focus on sustainability. The study will investigate the feasibility and efficiency of these techniques, considering factors such as selectivity, energy consumption, waste generation, and scalability. The findings of this research will contribute to the development of more sustainable and efficient separation processes in the pharmaceutical industry.

Chapter 1: Introduction
1.1 Background and significance of pharmaceutical compound purification
1.2 Overview of traditional separation techniques and their limitations
1.3 Importance of sustainable separation processes in the pharmaceutical industry
1.4 Research objectives and methodology

Chapter 2: Literature Review
2.1 Overview of pharmaceutical compound purification techniques
2.2 Analysis of traditional separation techniques and their drawbacks
2.3 Review of recent advancements in novel separation techniques
2.4 Evaluation of sustainability aspects in pharmaceutical compound purification

Chapter 3: Novel Separation Techniques
3.1 Membrane-based separation techniques
3.2 Supercritical fluid extraction
3.3 Adsorption and chromatographic techniques
3.4 Hybrid separation processes
3.5 Comparative analysis of novel techniques with traditional methods

Chapter 4: Feasibility and Efficiency Analysis
4.1 Experimental setup and methodology
4.2 Evaluation of selectivity and purity achieved by novel separation techniques
4.3 Energy consumption analysis of different separation processes
4.4 Assessment of waste generation and environmental impact
4.5 Techno-economic analysis and scalability considerations

Chapter 5: Optimization and Future Directions
5.1 Optimization strategies for enhancing the efficiency of novel separation techniques
5.2 Integration of sustainable separation processes into pharmaceutical manufacturing
5.3 Challenges and potential solutions for industrial implementation
5.4 Future research directions and opportunities for further improvement

Note: The chapter titles and content can be adjusted based on the specific focus and scope of the research project.