Supersaturation tracking for the development, optimization and control of crystallization processes

被引:66
作者
Barrett, Mark [1 ]
McNamara, Mairtin [1 ]
Hao, HongXun [1 ]
Barrett, Paul [2 ]
Glennon, Brian [1 ]
机构
[1] Natl Univ Ireland Univ Coll Dublin, Sch Chem & Bioproc Engn, Dublin 4, Ireland
[2] Univ Queensland, Brisbane, Qld, Australia
基金
爱尔兰科学基金会;
关键词
Supersaturation; Crystallization; ATR-FTIR; FBRM; Feedback control; Scale-up; ATR-FTIR SPECTROSCOPY; BATCH COOLING CRYSTALLIZATION; PROCESS ANALYTICAL TECHNOLOGY; METASTABLE ZONE WIDTH; IN-SITU; ANTISOLVENT CRYSTALLIZATION; LASER BACKSCATTERING; DIRECT DESIGN; TEMPERATURE; FBRM;
D O I
10.1016/j.cherd.2010.02.010
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Supersaturation is the key driving force in crystallization operations, determining nucleation and growth kinetics, and heavily influencing physical mechanisms such as agglomeration. Therefore, knowledge of the bulk supersaturation during crystallization can greatly enhance process understanding and optimization. In this paper, a method which facilitates the calibration-free use of in situ ATR-FTIR for crystallization development and control is presented. This methodology uses solute-specific ATR-FTIR absorption peak heights to describe solute solubility and dissolved concentration and, in turn, supersaturation, for the optimization of cooling crystallizations of an active pharmaceutical ingredient (API) and benzoic acid. The approach presented facilitates rapid process understanding, design and optimization. Specifically, the potential to significantly reduce cycle time for both systems studies is demonstrated. In addition, the potential of the method to form the basis of a process control strategy for batch crystallization is successfully demonstrated. (C) 2010 The Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1108 / 1119
页数:12
相关论文
共 30 条
[1]   The Impact of Direct Nucleation Control on Crystal Size Distribution in Pharmaceutical Crystallization Processes [J].
Abu Bakar, Mohd R. ;
Nagy, Zoltan K. ;
Saleemi, Ali N. ;
Rielly, Chris D. .
CRYSTAL GROWTH & DESIGN, 2009, 9 (03) :1378-1384
[2]  
BARRETT M, 2008, THESIS U COLL DUBLIN
[3]   Characterizing the metastable zone width and solubility curve using lasentec FBRM and PVM [J].
Barrett, P ;
Glennon, B .
CHEMICAL ENGINEERING RESEARCH & DESIGN, 2002, 80 (A7) :799-805
[4]   On-line monitoring of batch cooling crystallization of organic compounds using ATR-FTIR spectroscopy coupled with an advanced calibration method [J].
Chen, Zeng-Ping ;
Morris, Julian ;
Borissova, Antonia ;
Khan, Shahid ;
Mahmud, Tariq ;
Penchev, Rado ;
Roberts, Kevin J. .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 2009, 96 (01) :49-58
[5]   Automated in-line technique using FBRM to achieve consistent product quality in cooling crystallization [J].
Chew, Jia Wei ;
Chow, Pui Shan ;
Tan, Reginald B. H. .
CRYSTAL GROWTH & DESIGN, 2007, 7 (08) :1416-1422
[6]   Comparison between open-loop temperature control and closed-loop supersaturation control for cooling crystallization of glycine [J].
Chew, Jia Wei ;
Black, Simon N. ;
Chow, Pui Shan ;
Tan, Reginald B. H. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2007, 46 (03) :830-838
[7]   Quantitative application of in situ ATR-FTIR and Raman spectroscopy in crystallization processes [J].
Cornel, Jeroen ;
Lindenberg, Christian ;
Mazzotti, Marco .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2008, 47 (14) :4870-4882
[8]   A Novel Crystallization Methodology To Ensure Isolation of the Most Stable Crystal Form [J].
Cote, Aaron ;
Zhou, George ;
Stanik, Mary .
ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2009, 13 (06) :1276-1283
[9]   ATR FTIR spectroscopy for in situ measurement of supersaturation [J].
Dunuwila, DD ;
Berglund, KA .
JOURNAL OF CRYSTAL GROWTH, 1997, 179 (1-2) :185-193
[10]   First-principles and direct design approaches for the control of pharmaceutical crystallization [J].
Fujiwara, M ;
Nagy, ZK ;
Chew, JW ;
Braatz, RD .
JOURNAL OF PROCESS CONTROL, 2005, 15 (05) :493-504