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Download fileDesign and Optimization of the Single-Stage Continuous Mixed Suspension–Mixed Product Removal Crystallization of 2‑Chloro‑N‑(4-methylphenyl)propenamide
journal contribution
posted on 2022-04-13, 22:44 authored by Gladys
Kate Pascual, Philip Donnellan, Brian Glennon, Barbara Wood, Roderick C. JonesA continuously operated
single-stage mixed suspension–mixed
product removal (MSMPR) crystallizer was developed for the continuous
cooling crystallization of 2-chloro-N-(4-methylphenyl)propanamide
(CNMP) in toluene from 25 to 0 °C. The conversion of the previous
batch to a continuous process was key to developing a methodology
linking the synthesis and purification unit operations of CNMP and
gave further insight in the development of continuous process trains
for active pharmaceutical ingredient materials. By monitoring how
parameters such as cooling and agitation rates influence particle
size and the yield, two batch start-up strategies were compared. The
second part of the study focused on developing and optimizing the
continuous cooling crystallization of CNMP in the MSMPR crystallizer
in relation to the yield by determining the effects of varying the
residence time and the agitation rates. During the MSMPR operation,
the plot of the focused beam reflectance measurement total counts
versus time oscillates and reaches an unusual state of control. Despite
the oscillations, the dissolved concentration was constant. The yield
and production rate from the system were constant after two residence
times, as supported by FTIR data. The overall productivity was higher
at shorter residence times (τ), and a productivity of 69.51
g/h for τ = 20 min was achieved for the isolation of CNMP.
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purification unit operations0 ° ctwo residence timesshorter residence timestwo batch startcontinuous process trainsmethylphenyl ) propanamidecontinuously operated singlecontinuous cooling crystallizationcontinuous processresidence timeprevious batchunusual statestudy focusedsecond partproduction raten </methodology linkingftir datadissolved concentrationchloro -<agitation rates>‑( 4>-( 451 g20 min