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Статті в журналах з теми "Crystallization systems"
Balonin, Nikolay A., Victor S. Suzdal, and Yuriy S. Kozmin. "Modal Control of Crystallization Systems." Journal of Automation and Information Sciences 46, no. 8 (2014): 10–17. http://dx.doi.org/10.1615/jautomatinfscien.v46.i8.20.
Повний текст джерелаSHIOMI, TOMOO. "Crystallization in Multiphase Polymer Systems." Sen'i Gakkaishi 55, no. 3 (1999): P87—P91. http://dx.doi.org/10.2115/fiber.55.3_p87.
Повний текст джерелаSanjoh, Akira. "PCMOS - Protein Crystallization Microfluidic Systems." Acta Crystallographica Section D Biological Crystallography 58, no. 10 (September 26, 2002): 1763. http://dx.doi.org/10.1107/s0907444902014890.
Повний текст джерелаBARD, J. "Automated systems for protein crystallization." Methods 34, no. 3 (November 2004): 329–47. http://dx.doi.org/10.1016/j.ymeth.2004.03.029.
Повний текст джерелаRibeiro, Ana Paula Badan, Monise Helen Masuchi, Eriksen Koji Miyasaki, Maria Aliciane Fontenele Domingues, Valter Luís Zuliani Stroppa, Glazieli Marangoni de Oliveira, and Theo Guenter Kieckbusch. "Crystallization modifiers in lipid systems." Journal of Food Science and Technology 52, no. 7 (October 11, 2014): 3925–46. http://dx.doi.org/10.1007/s13197-014-1587-0.
Повний текст джерелаVos, Max A. "Crystallization in natural silicate systems." Journal of Non-Crystalline Solids 84, no. 1-3 (July 1986): 318–19. http://dx.doi.org/10.1016/0022-3093(86)90791-x.
Повний текст джерелаWibowo, Christianto, Wen-Chi Chang, and Ka M. Ng. "Design of integrated crystallization systems." AIChE Journal 47, no. 11 (November 2001): 2474–92. http://dx.doi.org/10.1002/aic.690471111.
Повний текст джерелаNewman, Janet. "Novel buffer systems for macromolecular crystallization." Acta Crystallographica Section D Biological Crystallography 60, no. 3 (February 25, 2004): 610–12. http://dx.doi.org/10.1107/s0907444903029640.
Повний текст джерелаAngell, C. A., and Y. Choi. "Crystallization and vitrification in aqueous systems." Journal of Microscopy 141, no. 3 (March 1986): 251–61. http://dx.doi.org/10.1111/j.1365-2818.1986.tb02720.x.
Повний текст джерелаMalinina, L. V., V. V. Makhaldiani, V. A. Tereshko, V. F. Zarytova, and E. M. Ivanova. "Phase Diagrams for DNA Crystallization Systems." Journal of Biomolecular Structure and Dynamics 5, no. 2 (October 1987): 405–33. http://dx.doi.org/10.1080/07391102.1987.10506402.
Повний текст джерелаДисертації з теми "Crystallization systems"
Saleemi, Ali Nauman. "Strategic feedback control of pharmaceutical crystallization systems." Thesis, Loughborough University, 2011. https://dspace.lboro.ac.uk/2134/8530.
Повний текст джерелаSheikh, Ahmad Yahya. "Synthesis, optimisation and control of crystallization systems." Thesis, University College London (University of London), 1997. http://discovery.ucl.ac.uk/1317664/.
Повний текст джерелаMontenegro, Rivelino V. D. "Crystallization, biomimetics and semiconducting polymers in confined systems." Phd thesis, Universität Potsdam, 2003. http://opus.kobv.de/ubp/volltexte/2005/76/.
Повний текст джерелаKristallisation, Biomimetik und halbleitende Polymere in räumlich begrenzten Systemen:
Öl und Wasser mischen sich nicht, man kann aber aus beiden Flüssigkeiten Emulsionen herstellen, bei denen Tröpfchen der einen Flüssigkeit in der anderen Flüssigkeit vorliegen. Das heißt, es können entweder Öltröpfchen in Wasser oder Wassertröpfchen in Öl erzeugt werden. Aus täglichen Erfahrungen, z.B. beim Kochen weiß man jedoch, dass sich eine Emulsion durch Schütteln oder Rühren herstellen lässt, diese jedoch nicht besonders stabil ist. Mit Hilfe von hohen Scherenergien kann man nun sehr kleine, in ihrer Größe sehr einheitliche und außerdem sehr stabile Tröpfchen von 1/10000 mm erhalten. Eine solche Emulsion wird Miniemulsion genannt.
In der Dissertation wurden nun z.B. Miniemulsionen untersucht, die aus kleinen Wassertröpfchen in einem Öl bestehen. Es konnte gezeigt werden, dass das Wasser in diesen Tröpfchen, also in den räumlich begrenzten Systemen, nicht bei 0 °C, sondern bei -22 °C kristallisierte. Wie lässt sich das erklären? Wenn man einen Eimer Wasser hat, dann bildet sich normalerweise bei 0 °C Eis, da nämlich in dem Wasser einige (manchmal ganz wenige) Keime (z.B. Schutzteilchen, ein Fussel etc.) vorhanden sind, an denen sich die ersten Kristalle bilden. Wenn sich dann einmal ein Kristall gebildet hat, kann das Wasser im gesamten Eimer schnell zu Eis werden. Ultrareines Wasser würde bei -22 °C kristallisieren. Wenn man jetzt die Menge Wasser aus dem Eimer in kleine Tröpfchen bringt, dann hat man eine sehr, sehr große Zahl, nämlich 1017 Tröpfchen, in einem Liter Emulsion vorliegen. Die wenigen Schmutzpartikel verteilen auf sehr wenige Tröpfchen, die anderen Tröpfchen sind ultrarein. Daher kristallisieren sie erst bei -22 °C.
Im Rahmen der Arbeit konnte auch gezeigt werden, dass die Miniemulsionen genutzt werden können, um kleine Gelatine-Partikel, also Nanogummibärchen, herzustellen. Diese Nanogummibärchen quellen bei Erhöhung der Temperatur auf ca. 38 °C an. Das kann ausgenutzt werden, um zum Beispiel Medikamente zunächst in den Partikeln im menschlichen Körper zu transportieren, die Medikamente werden dann an einer gewünschten Stelle freigelassen. In der Arbeit wurde auch gezeigt, dass die Gelatine-Partikel genutzt werden können, um die Natur nachzuahnen (Biomimetik). Innerhalb der Partikel kann nämlich gezielt Knochenmaterial aufgebaut werden kann. Die Gelatine-Knochen-Partikel können dazu genutzt werden, um schwer heilende oder komplizierte Knochenbrüche zu beheben. Gelatine wird nämlich nach einigen Tagen abgebaut, das Knochenmaterial kann in den Knochen eingebaut werden.
LEDs werden heute bereits vielfältig verwendet. LEDs bestehen aus Halbleitern, wie z.B. Silizium. Neuerdings werden dazu auch halbleitende Polymere eingesetzt. Das große Problem bei diesen Materialien ist, dass sie aus Lösungsmitteln aufgebracht werden. Im Rahmen der Doktorarbeit wurde gezeigt, dass der Prozess der Miniemulsionen genutzt werden kann, um umweltfreundlich diese LEDs herzustellen. Man stellt dazu nun wässrige Dispersionen mit den Polymerpartikeln her. Damit hat man nicht nur das Lösungsmittel vermieden, das hat nun noch einen weiteren Vorteil: man kann nämlich diese Dispersion auf sehr einfache Art verdrucken, im einfachsten Fall verwendet man einfach einen handelsüblichen Tintenstrahldrucker.
The colloidal systems are present everywhere in many varieties such as emulsions (liquid droplets dispersed in liquid), aerosols (liquid dispersed in gas), foam (gas in liquid), etc. Among several new methods for the preparation of colloids, the so-called miniemulsion technique has been shown to be one of the most promising. Miniemulsions are defined as stable emulsions consisting of droplets with a size of 50-500 nm by shearing a system containing oil, water, a surfactant, and a highly water insoluble compound, the so-called hydrophobe
1. In the first part of this work, dynamic crystallization and melting experiments are described which were performed in small, stable and narrowly distributed nanodroplets (confined systems) of miniemulsions. Both regular and inverse systems were examined, characterizing, first, the crystallization of hexadecane, secondly, the crystallization of ice. It was shown for both cases that the temperature of crystallization in such droplets is significantly decreased (or the required undercooling is increased) as compared to the bulk material. This was attributed to a very effective suppression of heterogeneous nucleation. It was also found that the required undercooling depends on the nanodroplet size: with decreasing droplet size the undercooling increases.
2. It is shown that the temperature of crystallization of other n-alkanes in nanodroplets is also significantly decreased as compared to the bulk material due to a very effective suppression of heterogeneous nucleation. A very different behavior was detected between odd and even alkanes. In even alkanes, the confinement in small droplets changes the crystal structure from a triclinic (as seen in bulk) to an orthorhombic structure, which is attributed to finite size effects inside the droplets. An intermediate metastable rotator phase is of less relevance for the miniemulsion droplets than in the bulk. For odd alkanes, only a strong temperature shift compared to the bulk system is observed, but no structure change. A triclinic structure is formed both in bulk and in miniemulsion droplets.
3. In the next part of the thesis it is shown how miniemulsions could be successfully applied in the development of materials with potential application in pharmaceutical and medical fields. The production of cross-linked gelatin nanoparticles is feasible. Starting from an inverse miniemulsion, the softness of the particles can be controlled by varying the initial concentration, amount of cross-link agent, time of cross-linking, among other parameters. Such particles show a thermo-reversible effect, e.g. the particles swell in water above 37 °C and shrink below this temperature. Above 37 °C the chains loose the physical cross-linking, however the particles do not loose their integrity, because of the chemical cross-linking. Those particles have potential use as drug carriers, since gelatin is a natural polymer derived from collagen.
4. The cross-linked gelatin nanoparticles have been used for the biomineralization of hydroxyapatite (HAP), a biomineral, which is the major constituent of our bones. The biomineralization of HAP crystals within the gelatin nanoparticles results in a hybrid material, which has potential use as a bone repair material.
5. In the last part of this work we have shown that layers of conjugated semiconducting polymers can be deposited from aqueous dispersion prepared by the miniemulsion process. Dispersions of particles of different conjugated semiconducting polymers such as a ladder-type poly(para-phenylene) and several soluble derivatives of polyfluorene could be prepared with well-controlled particle sizes ranging between 70 - 250 nm. Layers of polymer blends were prepared with controlled lateral dimensions of phase separation on sub-micrometer scales, utilizing either a mixture of single component nanoparticles or nanoparticles containing two polymers. From the results of energy transfer it is demonstrated that blending two polymers in the same particle leads to a higher efficiency due to the better contact between the polymers. Such an effect is of great interest for the fabrication of opto-electronic devices such as light emitting diodes with nanometer size emitting points and solar cells comprising of blends of electron donating and electron accepting polymers.
Succaw, Gary Lee. "Dynamics of crystal growth of self-assembling systems /." view abstract or download file of text, 2004. http://wwwlib.umi.com/cr/uoregon/fullcit?p3136448.
Повний текст джерелаTypescript. Includes vita and abstract. Includes bibliographical references (leaves 209-215). Also available for download via the World Wide Web; free to University of Oregon users.
Sultana, Mahmooda. "Microfluidic systems for continuous crystallization of small organic molecules." Thesis, Massachusetts Institute of Technology, 2010. http://hdl.handle.net/1721.1/59879.
Повний текст джерелаCataloged from PDF version of thesis.
Includes bibliographical references.
This thesis presents one of the first demonstrations of continuous crystallization in microfluidic devices, and illustrates their use for various applications related to crystallization of small organic molecules. Crystallization is an important process in a number of industries, including specialty chemicals, food, cosmetics, nutraceuticals and, most importantly, pharmaceuticals. Most small molecule pharmaceuticals are isolated in crystalline form, and more than ninety percent of all pharmaceutical products are formulated in particulate, mainly crystalline form. However, crystallization is not a completely understood process. The sensitivity of the process to synthesis conditions gives rise to serious reproducibility issues. The traditional batch crystallizers suffer from non-uniform process conditions across the reactor, and chaotic, poorly controlled mixing of the reagents, often resulting in polydisperse crystal size distribution and impure polymorphs. This makes it difficult to obtain reliable information on the process kinetics that can be used for scale-up, as well as to study the fundamentals of the process. Microfluidic systems offer a unique toolset for crystallization because of well-defined laminar flow profiles, enhanced heat and mass transfer, better control over the contact mode of the reagents, and optical access for in situ characterization. The better control over the synthesis conditions gives rise to the potential for controlling the crystal size, as well as the polymorphic form. In addition, low consumption of reagents makes it an attractive research tool for expensive pharmaceutical compounds. Some of the advantages of microfluidics have been demonstrated for crystallization in micro-batches, but so far not in continuous devices. Continuous crystallization is difficult to achieve in microchannels as uncontrolled nucleation, crystal growth, agglomeration and sedimentation of crystals easily clog the small channels. The interaction of crystals with channel walls may also contribute to channel plugging in these devices. This thesis has developed microfluidic devices for continuous crystallization of small organic molecules for the first time. We have decoupled nucleation and growth, the two key steps of crystallization, using reaction engineering principles, and have developed two separate continuous devices, one for each of these two processes. We have used seeded crystallization and reactor design to achieve controlled growth, as well as to suppress secondary nucleation, agglomeration and sedimentation of crystals. In addition, we have eliminated any significant interaction of crystals with channel walls by controlling the properties of channel surfaces. We have also integrated microscopy and spectroscopy tools with the device for in-situ characterization of crystal size and polymorphic form. We have illustrated the use of these devices to extract growth kinetics data for crystals of various shapes, including high aspect ratio systems such as that with acicular or plate-like habits. The reproducibility and control in our devices have allowed us to elucidate the growth mechanism and fundamentals of the growth process for difficult crystal systems. In addition, we have demonstrated that continuous microfluidic devices offer a unique advantage over the current state-of-the art technology to measure the size, size distribution and growth kinetics of high aspect ratio crystal systems more accurately. Moreover, we have demonstrated the use of microfluidic devices for understanding crystal habit modification in the presence of impurities. We take advantage of the high spatiotemporal resolution of microfluidic devices to study the evolution of crystal habit over time, and to obtain information on the kinetics of habit modification in the presence of different impurities. We have developed an understanding of the habit modification mechanism for alpha glycine in the presence of alpha amino acids. Such information may not only provide insights into impurity-crystal interactions, but also serve as a powerful tool for the design of impurities that can be deliberately added to improve the crystallization process. Furthermore, we have designed and developed a second microfluidic device for continuous supercritical crystallization for the first time. Using supercritical fluid as an antisolvent, we have demonstrated continuous spontaneous nucleation of acetaminophen. We have shown the ability to produce micron-sized crystals, which may be useful for increasing the bioavailability of drugs with lower solubility, as well as for inhalable and highly potent drugs with stringent size requirements. The developed platform can also be used as a high-throughput device for safely screening crystallization conditions in the supercritical domain. We have demonstrated such use by screening the effects of pressure and various solvents on the habit, size and polymorphic form of acetaminophen crystals.
by Mahmooda Sultana.
Ph.D.
Chavez, Krystle J. "Crystallization of pseudopolymorphic forms of sodium naproxen in mixed solvent systems." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2009. http://hdl.handle.net/1853/29759.
Повний текст джерелаCommittee Chair: Rousseau, Ronald; Committee Member: Meredith, Carson; Committee Member: Prausnitz, Mark; Committee Member: Teja, Amyn; Committee Member: Wilkinson, Angus. Part of the SMARTech Electronic Thesis and Dissertation Collection.
Antonello, Alice [Verfasser]. "Crystallization of complex inorganic systems within the confinement of miniemulsion droplets / Alice Antonello." Mainz : Universitätsbibliothek Mainz, 2017. http://d-nb.info/1136638776/34.
Повний текст джерелаShank, Dale. "Evaluating carbon dioxide as a causative agent of otolith crystallization in recirculating aquaculture systems." Bowling Green State University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1603716784275007.
Повний текст джерелаBöbel, Alexander [Verfasser], and Gregor [Akademischer Betreuer] Morfill. "Crystallization and demixing: morphological structure analysis in many-body systems / Alexander Böbel ; Betreuer: Gregor Morfill." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2018. http://d-nb.info/1173616233/34.
Повний текст джерелаCarr, Joel Matthew. "CONFINED LAYERED POLYMERIC SYSTEMS FOR PACKAGING ANDCAPACITOR APPLICATIONS." Case Western Reserve University School of Graduate Studies / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=case1363104386.
Повний текст джерелаКниги з теми "Crystallization systems"
Crystallization process systems. Oxford: Butterworth-Heinemann, 2002.
Знайти повний текст джерелаBorn, Philip G. Crystallization of Nanoscaled Colloids. Heidelberg: Springer International Publishing, 2013.
Знайти повний текст джерелаFarrow, Robin F. C. Magnetism and structure in systems of reduced dimension. Boston, MA: Springer, 1993.
Знайти повний текст джерелаThe crystallization of the Arab state system, 1945-1954. Syracuse: Syracuse University Press, 1993.
Знайти повний текст джерелаVargin, V. V., ред. Catalyzed Controlled Crystallization of Glasses in the Lithium Aluminosilicate System / Katalizirovannaya Reguliruemaya Kristallizatsiya Stekol Litievoalyumosilikatnoi Sistemy / Катализированная Регулируемая Кристаллизация Стекол Литиеволюмосиликатной Системы. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-4908-0.
Повний текст джерелаJ, Kelly M. Low-dimensional semiconductors: Materials, physics, technology, devices. Oxford: Clarendon Press, 1995.
Знайти повний текст джерелаJones, Alan G. Crystallization Process Systems. Elsevier Science & Technology Books, 2015.
Знайти повний текст джерелаJones, Alan G. Crystallization Process Systems. Elsevier Science & Technology Books, 2002.
Знайти повний текст джерелаThomas, Sabu, Nandakumar Kalarikkal, P. Mohammed Arif, and E. Bhoje Gowd. Crystallization in Multiphase Polymer Systems. Elsevier Science & Technology Books, 2017.
Знайти повний текст джерелаCrystallization in Multiphase Polymer Systems. Elsevier, 2018. http://dx.doi.org/10.1016/c2015-0-04665-2.
Повний текст джерелаЧастини книг з теми "Crystallization systems"
Hilfiker, Rolf. "Polymorphism of Crystalline Systems." In Crystallization, 85–103. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527650323.ch5.
Повний текст джерелаCimmino, S., E. Pace, E. Martuscelli, and C. Silvestre. "Crystallization of Multicomponent Polymer Systems." In Crystallization of Polymers, 381–402. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1950-4_35.
Повний текст джерелаde Jeu, Wim H. "Lamellar Ethylene Oxide-Butadiene Block Copolymer Films as Model Systems for Confined Crystallisation." In Polymer Crystallization, 196–207. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/3-540-45851-4_11.
Повний текст джерелаAbbas, Ali, Jose Romagnoli, and David Widenski. "Modeling of Crystallization Processes." In Process Systems Engineering, 239–85. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527631209.ch68.
Повний текст джерелаAbbas, Ali, Jose Romagnoli, and David Widenski. "Modeling of Crystallization Processes." In Process Systems Engineering, 239–85. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527631339.ch8.
Повний текст джерелаVarga, Jozsef. "β-Modification of Polypropylene and Its Two-Component Systems." In Crystallization of Polymers, 599–608. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1950-4_63.
Повний текст джерелаMüller, Alejandro J., Maria Luisa Arnal, and Arnaldo T. Lorenzo. "Crystallization in Nano-Confined Polymeric Systems." In Handbook of Polymer Crystallization, 347–78. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118541838.ch12.
Повний текст джерелаHoyer, Walter, Ivan Kaban, and Markus Merkwitz. "Liquid-Liquid Interfacial Tension and Wetting in Immiscible Al-Based Systems." In Solidification and Crystallization, 110–18. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603506.ch13.
Повний текст джерелаBayés-García, Laura, Teresa Calvet, and Miquel À. Cuevas-Diarte. "Effects of Dynamic Temperature Variations on Microstructure and Polymorphic Behavior of Lipid Systems." In Crystallization of Lipids, 183–210. Chichester, UK: John Wiley & Sons, Ltd, 2018. http://dx.doi.org/10.1002/9781118593882.ch6.
Повний текст джерелаAzizi Topkanlo, Hasan, Zahed Ahamadi, and Faramarz Afshar Taromi. "PET/PLA Blends Crystallization Kinetics." In Eco-friendly and Smart Polymer Systems, 682–85. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-45085-4_164.
Повний текст джерелаТези доповідей конференцій з теми "Crystallization systems"
Knowles, David, and Brian Klene. "Laser Crystallization for Flat Panel Displays." In Photonic Applications Systems Technologies Conference. Washington, D.C.: OSA, 2006. http://dx.doi.org/10.1364/phast.2006.ptub1.
Повний текст джерелаBray, Terry, Deborah Powell, Larry Kim, Rita Gray, Tam Le, Raymond Askew, Michael Harrington, William Rosenblum, W. Wilson, and Lawrence DeLucas. "New crystallization systems envisioned for microgravity studies." In Space Programs and Technologies Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1995. http://dx.doi.org/10.2514/6.1995-3582.
Повний текст джерелаRichard, Patrick, Annie Gervois, Luc Oger, and Jean-Paul Troadec. "Crystallization in hard sphere systems: A structural analysis." In PHYSICS OF GLASSES. ASCE, 1999. http://dx.doi.org/10.1063/1.1301469.
Повний текст джерелаPutis, Sergey, Andrey Mershin, Sergey Dushenok, Aleksandr Krasnov, and Tat’yana Vidyaeva. "A NEW METHOD OF CRYSTALLIZATION OF HNIW." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m795.aks-2019/375-377.
Повний текст джерелаTao Xu, Prasanna Thwar, Vijay Srinivasan, Vamsee K. Pamula, and Krishnendu Chakrabarty. "Digital microfluidic biochip design for protein crystallization." In 2007 IEEE/NIH Life Science Systems and Applications Workshop. IEEE, 2007. http://dx.doi.org/10.1109/lssa.2007.4400904.
Повний текст джерелаMaeno, Yoshiharu, and Yukio Ohsawa. "Stable Deterministic Crystallization for Discovering Hidden Hubs." In 2006 IEEE International Conference on Systems, Man and Cybernetics. IEEE, 2006. http://dx.doi.org/10.1109/icsmc.2006.384911.
Повний текст джерелаHsu, Y. W., C. H. Chen, and S. K. Fan. "Programmable protein crystallization in metered encapsulated droplets." In 2012 IEEE 25th International Conference on Micro Electro Mechanical Systems (MEMS). IEEE, 2012. http://dx.doi.org/10.1109/memsys.2012.6170197.
Повний текст джерелаSuarez, Luis Alberto Paz, Petia Georgieva, and Sebastião Feyo de Azevedo. "Intelligent Predictive Control - Application to Scheduled Crystallization Processes." In 2009 International Conference on Adaptive and Intelligent Systems (ICAIS). IEEE, 2009. http://dx.doi.org/10.1109/icais.2009.34.
Повний текст джерелаKawasaki, T., T. Araki, H. Tanaka, Michio Tokuyama, Irwin Oppenheim, and Hideya Nishiyama. "Link between Vitrification and Crystallization in Two Dimensional Polydisperse Colloidal Liquid." In COMPLEX SYSTEMS: 5th International Workshop on Complex Systems. AIP, 2008. http://dx.doi.org/10.1063/1.2897794.
Повний текст джерелаSOUZA, Anderson de Almeida, Leandro Seizo GLOVASKI, and Roberto Carlos de Castro SILVA. "CFD effectiveness of AUS32 crystallization prediction in SCR systems." In XXIV Simpósio Internacional de Engenharia Automotiva. São Paulo: Editora Edgard Blücher, 2016. http://dx.doi.org/10.5151/engpro-simea2016-pap85.
Повний текст джерелаЗвіти організацій з теми "Crystallization systems"
Cullinan, Timothy Edward. Crystallization dynamics in glass-forming systems. Office of Scientific and Technical Information (OSTI), February 2016. http://dx.doi.org/10.2172/1342537.
Повний текст джерелаNeyedley, K., J. J. Hanley, Z. Zajacz, and M. Fayek. Accessory mineral thermobarometry, trace element chemistry, and stable O isotope systematics, Mooshla Intrusive Complex (MIC), Doyon-Bousquet-LaRonde mining camp, Abitibi greenstone belt, Québec. Natural Resources Canada/CMSS/Information Management, 2021. http://dx.doi.org/10.4095/328986.
Повний текст джерелаBrenan, J. M., K. Woods, J. E. Mungall, and R. Weston. Origin of chromitites in the Esker Intrusive Complex, Ring of Fire Intrusive Suite, as revealed by chromite trace element chemistry and simple crystallization models. Natural Resources Canada/CMSS/Information Management, 2021. http://dx.doi.org/10.4095/328981.
Повний текст джерелаHERTING DL. FRACTIONAL CRYSTALLIZATION LABORATORY TESTING WITH INTERIM PRETREATMENT SYSTEM FEEDS. Office of Scientific and Technical Information (OSTI), September 2008. http://dx.doi.org/10.2172/938409.
Повний текст джерелаNeyedley, K., J. J. Hanley, P. Mercier-Langevin, and M. Fayek. Ore mineralogy, pyrite chemistry, and S isotope systematics of magmatic-hydrothermal Au mineralization associated with the Mooshla Intrusive Complex (MIC), Doyon-Bousquet-LaRonde mining camp, Abitibi greenstone belt, Québec. Natural Resources Canada/CMSS/Information Management, 2021. http://dx.doi.org/10.4095/328985.
Повний текст джерелаMohammadi, N., D. Corrigan, A. A. Sappin, and N. Rayner. Evidence for a Neoarchean to earliest-Paleoproterozoic mantle metasomatic event prior to formation of the Mesoproterozoic-age Strange Lake REE deposit, Newfoundland and Labrador, and Quebec, Canada. Natural Resources Canada/CMSS/Information Management, 2022. http://dx.doi.org/10.4095/330866.
Повний текст джерела