API Continuous Cooling and Antisolvent Crystallization for Kinetic Impurity Rejection in cGMP Manufacturing

2021 ◽  
Author(s):  
Martin D. Johnson ◽  
Christopher L. Burcham ◽  
Scott A. May ◽  
Joel R. Calvin ◽  
Jennifer McClary Groh ◽  
...  
Keyword(s):  
Continuous Cooling ◽  
Antisolvent Crystallization

Experimental Calibration & Multi-scale Simulation of Multi-modal γ′ Precipitation in Nickel Superalloys During Continuous Cooling

2021 ◽  
Vol 52 (7) ◽  
pp. 3122-3139
Author(s):  
Nicholas J. Krutz ◽  
Chen Shen ◽  
Carolin Fink ◽  
Jiashi Miao ◽  
Timothy Hanlon ◽  
...  
Keyword(s):  
Nickel Superalloys ◽  
Experimental Calibration ◽  
Continuous Cooling ◽  
Multi Scale

Investigation of Agglomeration in the Presence of Oiling Out in the Antisolvent Crystallization Process

2021 ◽  
Author(s):  
Liping Wang ◽  
Ying Bao ◽  
Zhuang Sun ◽  
Valerie J. Pinfield ◽  
Qiuxiang Yin ◽  
...  
Keyword(s):  
Crystallization Process ◽  
Antisolvent Crystallization

scholarly journals Optimization of the CCT Curves for Steels Containing Al, Cu and B

2021 ◽  
Author(s):  
Jyrki Miettinen ◽  
Sami Koskenniska ◽  
Mahesh Somani ◽  
Seppo Louhenkilpi ◽  
Aarne Pohjonen ◽  
...  
Keyword(s):  
Phase Transformation ◽  
Grain Boundary ◽  
Grain Boundaries ◽  
Austenite Decomposition ◽  
Final Phase ◽  
Cast Irons ◽  
Continuous Cooling Transformation ◽  
Continuous Cooling ◽  
Final Optimization ◽  
Cct Diagrams

AbstractNew continuous cooling transformation (CCT) equations have been optimized to calculate the start temperatures and critical cooling rates of phase formations during austenite decomposition in low-alloyed steels. Experimental CCT data from the literature were used for applying the recently developed method of calculating the grain boundary soluble compositions of the steels for optimization. These compositions, which are influenced by solute microsegregation and precipitation depending on the heating/cooling/holding process, are expected to control the start of the austenite decomposition, if initiated at the grain boundaries. The current optimization was carried out rigorously for an extended set of steels than used previously, besides including three new solute elements, Al, Cu and B, in the CCT-equations. The validity of the equations was, therefore, boosted not only due to the inclusion of new elements, but also due to the addition of more low-alloyed steels in the optimization. The final optimization was made with a mini-tab tool, which discarded statistically insignificant parameters from the equations and made them prudently safer to use. Using a thermodynamic-kinetic software, IDS, the new equations were further validated using new experimental CCT data measured in this study. The agreement is good both for the phase transformation start temperatures as well as the final phase fractions. In addition, IDS simulations were carried out to construct the CCT diagrams and the final phase fraction diagrams for 17 steels and two cast irons, in order to outline the influence of solute elements on the calculations and their relationship with literature recommendations.

scholarly journals Continuous Cooling Transformation Behaviour and Bainite Transformation Kinetics of 23CrNi3Mo Carburised Steel

Metals ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 48
Author(s):  
Wenjun Song ◽  
Min Lei ◽  
Mingpan Wan ◽  
Chaowen Huang
Keyword(s):  
Phase Transformation ◽  
Volume Fraction ◽  
Austenite Formation ◽  
Steel Matrix ◽  
Transformation Kinetics ◽  
Bainite Transformation ◽  
Continuous Cooling ◽  
The Matrix ◽  
Dimensional Growth ◽  
Kinetics Of

In this study, the phase transformation behaviour of the carburised layer and the matrix of 23CrNi3Mo steel was comparatively investigated by constructing continuous cooling transformation (CCT) diagram, determining the volume fraction of retained austenite (RA) and plotting dilatometric curves. The results indicated that Austenite formation start temperature (Ac1) and Austenite formation finish temperature (Ac3) of the carburised layer decreased compared to the matrix, and the critical cooling rate (0.05 °C/s) of martensite transformation is significantly lower than that (0.8 °C/s) of the matrix. The main products of phase transformation in both the carburised layer and the matrix were martensite and bainite microstructures. Moreover, an increase in carbon content resulted in the formation of lamellar martensite in the carburised layer, whereas the martensite in the matrix was still lath. Furthermore, the volume fraction of RA in the carburised layer was higher than that in the matrix. Moreover, the bainite transformation kinetics of the 23CrNi3Mo steel matrix during the continuous cooling process indicated that the mian mechanism of bainite transformation of the 23CrNi3Mo steel matrix is two-dimensional growth and one-dimensional growth.

scholarly journals Enhanced Water Solubility and Oral Bioavailability of Paclitaxel Crystal Powders through an Innovative Antisolvent Precipitation Process: Antisolvent Crystallization Using Ionic Liquids as Solvent

Pharmaceutics ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 1008 ◽  
Author(s):  
Qilei Yang ◽  
Chang Zu ◽  
Wengang Li ◽  
Weiwei Wu ◽  
Yunlong Ge ◽  
...  
Keyword(s):  
Oral Bioavailability ◽  
High Performance ◽  
Water Solubility ◽  
Water Soluble ◽  
Precipitation Process ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Antisolvent Precipitation ◽  
Antisolvent Crystallization ◽  
Artificial Gastric Juice

Paclitaxel (PTX) is a poor water-soluble antineoplastic drug with significant antitumor activity. However, its low bioavailability is a major obstacle for its biomedical applications. Thus, this experiment is designed to prepare PTX crystal powders through an antisolvent precipitation process using 1-hexyl-3-methylimidazolium bromide (HMImBr) as solvent and water as an antisolvent. The factors influencing saturation solubility of PTX crystal powders in water in water were optimized using a single-factor design. The optimum conditions for the antisolvent precipitation process were as follows: 50 mg/mL concentration of the PTX solution, 25 °C temperature, and 1:7 solvent-to-antisolvent ratio. The PTX crystal powders were characterized via scanning electron microscopy, Fourier transform infrared spectroscopy, high-performance liquid chromatography–mass spectrometry, X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, Raman spectroscopy, solid-state nuclear magnetic resonance, and dissolution and oral bioavailability studies. Results showed that the chemical structure of PTX crystal powders were unchanged; however, precipitation of the crystalline structure changed. The dissolution test showed that the dissolution rate and solubility of PTX crystal powders were nearly 3.21-folds higher compared to raw PTX in water, and 1.27 times higher in artificial gastric juice. Meanwhile, the bioavailability of PTX crystal increased 10.88 times than raw PTX. These results suggested that PTX crystal powders might have potential value to become a new oral PTX formulation with high bioavailability.

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