Switching to continuous production of fine chemicals and pharmaceuticals now made via batch operations promises significant advantages such as faster processing, better energy efficiency and smaller-size equipment. However, realistically assessing whether such a conversion makes sense can be difficult. Now, a team led by researchers at the Institute of Chemical and Engineering Sciences (ICES) at A*STAR, Singapore, claim to have developed a practical method to comprehensively evaluate existing batch processes to enable faster yet soundly based decisions about whether to convert to a continuous process.
The goal was not to optimize a given process from first principles but rather to efficiently identify a suitable process that meets business needs, explain the researchers.
“Our methodology makes understanding the process much clearer, especially to the chemists and engineers dealing with the synthesis,” notes Soo Khean Teoh of ICES. “It makes it easier to decide to proceed or kill the idea, minimizing wasted effort.”
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“The biggest challenge is that there is no ‘one-size-fits-all’ solution for changing from batch to continuous methods, because of the complex and varied chemistries involved,” comments Teoh. “We had to devise a method which guides users to understand the process in question, brainstorm about potential benefits, and help them come up with swift decisions.”
The methodology consists of three stages: initial screening, extended evaluation and process execution (Figure 1). The team already has applied the approach to three reactions with reasonably complex molecules.