z-logo
Premium
Particle Size Distributions and Performance of Preferential Crystallization of L‐ Asparagine·H 2 O with Tailor‐Made Additives
Author(s) -
Kongsamai Peetikamol,
Flood Chalongsri,
Horst Joop H.,
Flood Adrian E.
Publication year - 2018
Publication title -
chemical engineering and technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.403
H-Index - 81
eISSN - 1521-4125
pISSN - 0930-7516
DOI - 10.1002/ceat.201700668
Subject(s) - crystallization , yield (engineering) , enantiomer , particle size , chemistry , crystal (programming language) , aspartic acid , nuclear chemistry , crystallography , materials science , chemical engineering , stereochemistry , organic chemistry , amino acid , biochemistry , metallurgy , computer science , engineering , programming language
Preferential crystallization (PC) is a process to separate enantiomers. The efficiency of seeded, isothermal PC was enhanced using tailor‐made additives to inhibit the crystallization of the counter‐enantiomer. The inhibition of D‐ asparagine ( D‐ Asn) monohydrate using D‐ glutamic acid ( D‐ Glu) and D‐ aspartic acid ( D‐ Asp) as additives in PC was investigated by comparing the purity, yield, and particle size distribution after PC of L‐ Asn·H 2 O from DL‐ Asn·H 2 O. The amount of pure L‐ Asn·H 2 O solid product that can be produced before crystallization of the counter‐enantiomer is higher when using the additives D‐ Asp and D‐ Glu. However, the crystal size of L‐ Asn·H 2 O increases faster in PC without additives than in PC with additives. This means that the additives inhibit not only the crystallization of D‐ Asn·H 2 O but also the crystal growth of L‐ Asn·H 2 O.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom