Academic literature on the topic 'Nanoprecipitace'
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Journal articles on the topic "Nanoprecipitace"
Peng, Shenyou, Yujie Wei, and Huajian Gao. "Nanoscale precipitates as sustainable dislocation sources for enhanced ductility and high strength." Proceedings of the National Academy of Sciences 117, no. 10 (February 24, 2020): 5204–9. http://dx.doi.org/10.1073/pnas.1914615117.
Full textRuault, M.-O., F. Fortuna, H. Bernas, J. Chaumont, O. Kaïtasov, and V. A. Borodin. "In situ Transmission Electron Microscopy Ion Irradiation Studies at Orsay." Journal of Materials Research 20, no. 7 (July 1, 2005): 1758–68. http://dx.doi.org/10.1557/jmr.2005.0219.
Full textLi, Guoqiang, Shao-Ju Shih, Shichun Mu, Yadong Xu, and Wanqi Jie. "Study of Te nanoprecipitates in CdZnTe crystals." Journal of Materials Research 25, no. 7 (July 2010): 1298–303. http://dx.doi.org/10.1557/jmr.2010.0171.
Full textCourtney-Davies, Ciobanu, Verdugo-Ihl, Slattery, Cook, Dmitrijeva, Keyser, et al. "Zircon at the Nanoscale Records Metasomatic Processes Leading to Large Magmatic–Hydrothermal Ore Systems." Minerals 9, no. 6 (June 16, 2019): 364. http://dx.doi.org/10.3390/min9060364.
Full textPark, Ji-Hoon, Kee-Ahn Lee, Sung-Jae Won, Yong-Bum Kwon, and Kyou-Hyun Kim. "Influence of Sc Microalloying on the Microstructure of Al5083 Alloy and Its Strengthening Effect." Metals 11, no. 7 (July 14, 2021): 1120. http://dx.doi.org/10.3390/met11071120.
Full textWood, Jonathan. "Nanoprecipitate structure in Al alloys revealed." Materials Today 9, no. 6 (June 2006): 9. http://dx.doi.org/10.1016/s1369-7021(06)71527-9.
Full textHern, F. Y., A. Hill, A. Owen, and S. P. Rannard. "Co-initiated hyperbranched-polydendron building blocks for the direct nanoprecipitation of dendron-directed patchy particles with heterogeneous surface functionality." Polymer Chemistry 9, no. 14 (2018): 1767–71. http://dx.doi.org/10.1039/c8py00291f.
Full textBroad, Alexander, Ian J. Ford, Dorothy M. Duffy, and Robert Darkins. "Magnesium-rich nanoprecipitates in calcite: atomistic mechanisms responsible for toughening in Ophiocoma wendtii." Physical Chemistry Chemical Physics 22, no. 18 (2020): 10056–62. http://dx.doi.org/10.1039/d0cp00887g.
Full textDorignac, D., S. Schamm, C. Grigis, J. Sévely, J. Santiso, and A. Figueras. "Y2O3 nanoprecipitate/YBaCuO matrix interfaces: HREM study." Physica C: Superconductivity 235-240 (December 1994): 617–18. http://dx.doi.org/10.1016/0921-4534(94)91532-6.
Full textTang, Guodong, Qiang Wen, Teng Yang, Yang Cao, Wei Wei, Zhihe Wang, Zhidong Zhang, and Yusheng Li. "Rock-salt-type nanoprecipitates lead to high thermoelectric performance in undoped polycrystalline SnSe." RSC Advances 7, no. 14 (2017): 8258–63. http://dx.doi.org/10.1039/c7ra00140a.
Full textDissertations / Theses on the topic "Nanoprecipitace"
Xie, Ling. "Electron tomography analysis of 3D order and interfacial structure in nano-precipitates." Doctoral thesis, Uppsala universitet, Tillämpad materialvetenskap, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-284102.
Full textPereira, André Anderson Costa. "Desenvolvimento de sistema de atomização de solução polimérica em meio circulante para obtenção de partículas nano." PROGRAMA DE PÓS-GRADUAÇÃO EM ENGENHARIA QUÍMICA, 2018. https://repositorio.ufrn.br/jspui/handle/123456789/25447.
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
Partículas poliméricas formadas em escala nanométrica são de fundamental interesse atualmente, principalmente quando utilizadas como sistemas carreadores na liberação controlada de fármacos, cosméticos e nutracêuticos, bem como no recobrimento de matérias com propriedades magnéticas. O presente estudo tem como objetivo desenvolver um sistema para produção de partículas de poli (metacrilato de metila) (PMMA) e policaprolactona (PCL) a partir da atomização de solução polimérica em meio antisolvente. Neste sistema, soluções poliméricas em diferentes solventes são preparadas e atomizadas na forma de um spray. As gotículas geradas com a atomização entram em contato com um líquido antisolvente que provoca a precipitação e formação das partículas poliméricas. Neste trabalho, experimentos usando o sistema proposto foram realizados em diferentes condições operacionais e as partículas obtidas foram analisadas por espalhamento dinâmico de luz (Dynamic Light Scattering - DLS), microscopia eletrônica de transmissão (MET) e microscopia eletrônica de varredura (MEV). Os resultados demonstraram que é possível obter partículas com características de nanoesferas/nanocápsulas e nanofibras com distribuição de tamanho na faixa de 50 a 5000 nm. Também foi possível observar que as variáveis do processo como a natureza do polímero, o tipo de solvente (acetona, acetato de etila, álcool etílico, álcool isopropílico e álcool propílico), a pressão da atomização (0,25 – 3 bar) e a temperatura do líquido antisolvente (10 – 40°C) afetam diretamente a morfologia e a distribuição de tamanho de partícula (DTP). Além disso, foi avaliado o potencial de encapsulamento do sistema proposto. Óleo de algodão e aluminato de ferro (espinélio inverso) foram utilizados como material a ser encapsulado. As partículas produzidas nesta avaliação foram analisadas por DLS, MET, microscopia eletrônica de varredura com emissão de campo (MEV-FEG), espectroscopia de infravermelho com transformada de fourier (Fourier Transform Infrared Spectroscopy - FTIR) e difração de raios X (DRX) para a verificação do encapsulamento. De acordo com estes resultados, constatou-se a formação de partículas carreadoras, com características de nanocápsulas e nanoesferas. Ou seja, o material encapsulado pode ser encontrado dentro da partícula polimérica ou aderido a superfície da mesma, respectivamente.
Polymeric particles formed on a nanometric scale are of fundamental interest today, especially when used as carrier systems in the controlled release of drugs, cosmetics and nutraceuticals, as well as in the coating of materials with magnetic properties. The present study aims to develop a system for the production of poly (methyl methacrylate) (PMMA) and polycaprolactone (PCL) particles from the atomization of polymer solution in antisolvent medium. In this system, polymer solutions in different solvents are prepared and atomized in the form of a spray. The droplets generated with the atomization come into contact with an antisolvent liquid which causes the precipitation and formation of the polymer particles. In this work, experiments using the proposed system were performed under different operating conditions and the particles obtained were analyzed by Dynamic Light Scattering (DLS), transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The results demonstrated that it is possible to obtain particles with characteristics of nanospheres / nanocapsules and nanofibers with size distribution in the range of 50 to 5000 nm. It was also possible to observe that the process variables such as the nature of the polymer, type of solvent (acetone, ethyl acetate, ethyl alcohol, isopropyl alcohol and propyl alcohol), atomization pressure (0.25-3 bar) and antisolvent medium temperature (10-40°C) directly affect the morphology and particle size distribution (DTP). In addition, the potential of encapsulation of the proposed system was evaluated. Cotton oil and iron aluminate (inverse spinel) were used as the material to be encapsulated. The particles produced in this evaluation were analyzed by DLS, MET, field emission scanning electron microscopy (MEV-FEG), Fourier Transform Infrared Spectroscopy (FTIR) and X-ray diffraction (XRD) for the encapsulation check. According to these results, it was verified the formation of carrier particles, with characteristics of nanocapsules and nanospheres. That is, the encapsulated material can be found within the polymer particle or adhered to the surface thereof, respectively.
Širajová, Daniela. "Příprava polymerních fluorescenčních nanočástic." Master's thesis, 2021. http://www.nusl.cz/ntk/nusl-445759.
Full textKostíková, Katarína. "Studium vlivu povrchově aktivních látek na parametry polymerních nanočástic." Master's thesis, 2021. http://www.nusl.cz/ntk/nusl-446625.
Full textYang, Kuo-Cheng, and 楊國政. "Defect clusters, nanoprecipitates and Brownian motion of particles in Mg-doped Co1-xO, Ti-doped Co1-xO, Ti-doped MgO and Zr-doped TiO2." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/07470823059668375969.
Full text國立中山大學
材料科學研究所
93
In part I, MgO and Co1-xO powders in 9:1 and 1:9 molar ratio (denoted as M9C1 and M1C9 respectively) were sintered and homogenized at 1600oC followed by annealing at 850 and 800oC, respectively to form defect clusters and precipitates. Analytical electron microscopic (AEM) observations indicated the protoxide remained as rock salt structure with complicated planar diffraction contrast for M9C1 sample, however with spinel paracrystal precipitated from the M1C9 sample due to the assembly of charge- and volume-compensating defects of the 4:1 type, i.e. four octahedral vacant sites surrounding one Co3+-filled tetrahedral interstitial site. The spacing of such defect clusters is 4.5 times the lattice spacing of the average spinel structure of Mg-doped Co3-dO4, indicating a higher defect cluster concentration than undoped Co3-dO4. The {111} faulting of Mg-doped Co3-dO4/Co1-xO in the annealed M1C9 sample implies the possible presence of zinc blend-type defect clusters with cation vacancies assembled along oxygen close packed (111) plane. In part II, the Mg2TiO4/MgO composites prepared by reactive sintering MgO and TiO2 powders (9:1 molar ratio) at 1600oC and then air-cooled or further aged at 900oC were studied by X-ray diffraction and (AEM) in order to characterize the microstructures and formation mechanism of nanosized Mg2TiO4 spinel precipitated from Ti-doped MgO. Expulsion of Ti4+ during cooling caused the formation of (001)-specific G.P. zone under the influence of thermal/sintering stress and then the spinel precipitates, which were about 30 nm in size and nearly spherical with {111} and {100} facets to minimize coherency strain energy and surface energy. Secondary nano-size spinel was precipitated and became site saturated during aging at 900oC, leaving a precipitate free zone at the grain boundaries of Ti-doped MgO. The intergranular spinel became progressively Ti-richer upon aging 900oC and showed <110>-specific diffuse scatter intensity likely due to short range ordering and/or onset decomposition. In part III, the Co1-xO/Co2TiO4 composite prepared by reactive sintering CoO and TiO2 powders (9:1 molar ratio) at 1450oC and then air-cooled were studied by X-ray diffraction and AEM in order to characterize the microstructures and formation mechanism of nanosized Co2TiO4 spinel precipitated from Ti-doped Co1-xO. Slight expulsion of Ti4+ during cooling caused the precipitation of nanosize Co2TiO4 spinel. Bulk site saturation also caused impingement of the Co2TiO4 precipitates upon growth. The Co3-dO4 spinel, as an oxidatin product of Co1-xO, was found to form at free surface and the Co1-xO/Co2TiO4 interface. The Co2TiO4 spinel particles formed by reactive sintering rather than precipitation were able to detach from the Co1-xO grain boundaries to reach parallel epitaxial orientation with respect to the host Co1-xO grains via Brownian-type rotation of the embedded particles. In part IV, AEM was used to study the defect microstructures of Zr-dissolved TiO2 prepared via reactive sintering the ZrO2 and TiO2 powders (8:92 in molar ratio, designated as Z8T92) at 1600oC for 24 h and then aged at 900oC for 2-200 h in air. The Zr-dissolved TiO2 with rutile structure showed dislocation arrays, defect clusters, G.P. zone, superlattice, nanometer-size domains incommensurate and commensurate superstructure, may be the precursor of ZrTi2O6 precipitates at 900oC. The rutile showed diffuse diffractions along [001] direction as a result of Zr4+ substitution for Ti4+ with volume compensating defect clusters. Incommensurate and commensurate structures, as indicated by diffraction splitting and extra diffraction along <100> and <010> directions may be attributed to the ordering and clustering process of Zr and Ti atoms in these directions. Part V, deals with the reactive sintering of ZrO2 and TiO2 powders (1:4 molar ratio) at 1400 to 1600oC in air to form orthorhombic ZrTiO4 (a-PbO2-type structure, denoted as a) and to study its epitaxial reorientation in the matrix of tetragonal TiO2 (rutile) grains with Zr4+ (15 mol %) dissolution. The epitaxial relationship of intragranular ZrTiO4 and Zr-dissolved rutile (denoted as r) was determined by electron diffraction as [010]a//[011]r; (001)a // (011)r (i.e. [100]a // [100]r; (001)a // (011)r). The reorientation of the intragranular particles in the composites can be reasonably explained by rotation of the nonepitaxial particles above a critical temperature (T/Tm > 0.8) and below a critical particle size for anchorage release at interface with respect to the host grain. Reactive sintering facilitated the reoreientation process for the particles about to detach from the grain boundaries. The Brownian rotation of the confined ZrTiO4 particles in rutile grains was activated by a beneficial lower interfacial energy for the epitaxial relationship, typically forming lath-like ZrTiO4 with (101)a/(211)r habit plane having fair match of oxygen atoms at the interface. Further aging at 900oC for 50 h in air caused modulated and periodic antiphase domains in ZrTiO4 matrix, as likely precursor of equilibrium ZrTi2O6.
Book chapters on the topic "Nanoprecipitace"
Rivera-Diaz-del-Castillo, Pedro E. J., Maarten de Jong, and Marcel H. F. Sluiter. "Thermomechanical Processing Design of Nanoprecipitate Strengthened Alloys Employing Genetic Algorithms." In Supplemental Proceedings, 477–84. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118062142.ch58.
Full textDe Luca, Anthony, David C. Dunand, and David N. Seidman. "Scandium-Enriched Nanoprecipitates in Aluminum Providing Enhanced Coarsening and Creep Resistance." In The Minerals, Metals & Materials Series, 1589–94. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-72284-9_207.
Full textZhao, Y., Y. Cui, H. Guo, S. S. Xu, X. H. Wei, and Z. W. Zhang. "Effects of Aging Treatment on the Microstructure and Mechanical Properties of a Nanoprecipitates-Strengthened Ferritic Steel." In The Minerals, Metals & Materials Series, 27–37. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-72131-6_3.
Full textMajumdar, Shrabani, Kumar Sadanand Arya, Ashok Kumar, and P. V. Dilip. "Comparison of LCF Performance of a Ferritic Steel Strengthened with Nanoprecipitates with that of a Conventional HSLA Steel." In Lecture Notes in Mechanical Engineering, 663–69. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-8767-8_56.
Full text"Ripening among Nanoprecipitates." In Kinetics in Nanoscale Materials, 99–117. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118743140.ch4.
Full text"Energy-filtered imaging of Cu-nanoprecipitates." In Electron Microscopy and Analysis 2003, 255–58. CRC Press, 2004. http://dx.doi.org/10.1201/9781482269130-60.
Full textBERANGER, M., P. THEVENARD, R. BRENIER, B. CANUT, S. M. M. RAMOS, A. BRUNELLE, S. DELLA NEGRA, Y. LE BEYEC, and E. BALANZAT. "Mixing effects by electronic processes in MgO containing Na nanoprecipitates bombarded with GeV heavy ions and 20 MeV cluster beams." In Ion Beam Modification of Materials, 724–27. Elsevier, 1996. http://dx.doi.org/10.1016/b978-0-444-82334-2.50136-2.
Full textConference papers on the topic "Nanoprecipitace"
Stegailov, Vladimir V., Alexey Yu Kuksin, Genri E. Norman, Alexey V. Yanilkin, Mark Elert, Michael D. Furnish, Ricky Chau, Neil Holmes, and Jeffrey Nguyen. "ATOMISTIC STUDY OF NANOPRECIPITATES INFLUENCE ON PLASTICITY AND FRACTURE OF CRYSTALLINE METALS." In SHOCK COMPRESSION OF CONDENSED MATTER - 2007: Proceedings of the Conference of the American Physical Society Topical Group on Shock Compression of Condensed Matter. AIP, 2008. http://dx.doi.org/10.1063/1.2833049.
Full textKuhr, Samuel J. M., M. F. Pinnell, and Daniel Eylon. "Microstructural study of nanoprecipitates in RRA treated Al-7075 T6 using AFM/UFM/STEM." In NDE for Health Monitoring and Diagnostics, edited by Norbert Meyendorf, George Y. Baaklini, and Bernd Michel. SPIE, 2003. http://dx.doi.org/10.1117/12.484000.
Full textMedina-Almazán, A. Liliana, Lizandra S. Ovando-Ramírez, Rogelio Hernández-Callejas, and Gonzalo Galicia-Aguilar. "Hardness and Microstructural Evolution of a JRQ A533 Cl.1 Steel Submitted to Thermal Annealing." In ASME 2018 Pressure Vessels and Piping Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/pvp2018-84916.
Full textMedina Almazán, A. Liliana, Lizandra S. Ovando Ramírez, and Thierry Auger. "Hardness and Microstructural Evolution of a JRQ A533 Cl.1 Steel Submitted to Thermal Annealing." In ASME 2016 Pressure Vessels and Piping Conference. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/pvp2016-63303.
Full textReports on the topic "Nanoprecipitace"
Hamilton, John C. Edge energies and shapes of nanoprecipitates. Office of Scientific and Technical Information (OSTI), January 2006. http://dx.doi.org/10.2172/902203.
Full textTan, Lizhen, Ying Yang, Tianyi Chen, K. Sridharan, and Li He. Design and screening of nanoprecipitates-strengthened advanced ferritic alloys. Office of Scientific and Technical Information (OSTI), December 2016. http://dx.doi.org/10.2172/1341567.
Full textTan, Lizhen, Ying Yang, Tianyi Chen, Kumar Sridharam, and Li He. Mechanical Properties and Radiation Resistance of Nanoprecipitates-Strengthened Advanced Ferritic Alloys. Office of Scientific and Technical Information (OSTI), December 2017. http://dx.doi.org/10.2172/1427634.
Full textTan, Lizhen, Tianyi Chen, Ying Yang, Li He, and Kumar Sridharan. Development of nanoprecipitates-strengthened advanced ferritic alloys for nuclear reactor applications. Office of Scientific and Technical Information (OSTI), February 2019. http://dx.doi.org/10.2172/1526385.
Full textTan, Lizhen, Tianyi Chen, Ying Yang, Li He, and Kumar Sridharan. Report on the down-selected nanoprecipitates-strengthened advanced ferritic alloys for nuclear reactor applications. Office of Scientific and Technical Information (OSTI), February 2019. http://dx.doi.org/10.2172/1506786.
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