Relevant bibliographies by topics / 030306 Synthesis of Materials

Academic literature on the topic '030306 Synthesis of Materials'

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Published: 10 December 2022
Last updated: 29 January 2023

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Journal articles on the topic "030306 Synthesis of Materials"

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Rathinamala, I., J. Pandiarajan, N. Jeyakumaran, and N. Prithivikumaran. "Synthesis and Physical Properties of nanocrystalline CdS Thin Films – Influence of sol Aging Time & Annealing." International Journal of Thin Films Science and Technology 3, no. 3 (September 1, 2014): 113–20. http://dx.doi.org/10.12785/ijtfst/030306.

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Flynn, C. P., M. H. Yang, F. Tsui, Y. Lee, and R. L. Averback. "Materials science through materials synthesis." Journal of Physics and Chemistry of Solids 55, no. 10 (October 1994): 1059–66. http://dx.doi.org/10.1016/0022-3697(94)90124-4.

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Takeuchi, Ichiro, Jochen Lauterbach, and Michael J. Fasolka. "Combinatorial materials synthesis." Materials Today 8, no. 10 (October 2005): 18–26. http://dx.doi.org/10.1016/s1369-7021(05)71121-4.

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Shimakawa, Yuichi. "Synthesis of Powder Materials." Journal of the Japan Society of Powder and Powder Metallurgy 54, no. 1 (2007): 22. http://dx.doi.org/10.2497/jjspm.54.22.

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Bill, Joachim, and Fritz Aldinger. "Progress in Materials Synthesis." International Journal of Materials Research 87, no. 11 (November 1, 1996): 827–40. http://dx.doi.org/10.1515/ijmr-1996-871105.

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Manukyan, K. V. "Combustion and materials synthesis." International Journal of Self-Propagating High-Temperature Synthesis 26, no. 3 (July 2017): 143–44. http://dx.doi.org/10.3103/s1061386217030025.

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Byrappa, K., Richard E. Riman, and G. Dhanaraj. "Materials Synthesis – Novel Approaches." Materials Research Innovations 14, no. 1 (February 2010): 2. http://dx.doi.org/10.1179/143307510x12599329342881.

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Solozhenko, Vladimir L., and Eugene Gregoryanz. "Synthesis of superhard materials." Materials Today 8, no. 11 (November 2005): 44–51. http://dx.doi.org/10.1016/s1369-7021(05)71159-7.

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Dan, Nily. "Synthesis of hierarchical materials." Trends in Biotechnology 18, no. 9 (September 2000): 370–74. http://dx.doi.org/10.1016/s0167-7799(00)01482-7.

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Bill, J., and F. Aldinger. "Progress in materials synthesis." Metal Powder Report 52, no. 7-8 (July 1997): 38. http://dx.doi.org/10.1016/s0026-0657(97)80167-1.

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Dissertations / Theses on the topic "030306 Synthesis of Materials"

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Boase, Nathan R. B. "Hyperbranched polymers for in vivo multimodal molecular imaging." Thesis, University of Queensland, 2015. https://eprints.qut.edu.au/96267/1/96267.pdf.

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For the development of the next generation of polymeric nanomedicines, it is crucial to gain a fundamental understanding of their behaviour and interactions with and within biological systems. Moving beyond in vitro models, into in vivo models, earlier in the development process will greatly aid in the advancement of the next generation of nanomedicines. By moving to whole animal models, our understanding of these systems progresses beyond cell targeting and uptake, to developing mechanisms for how these materials will distribute through tissues and their pharmacokinetic profile. This information is important for truly assessing the performance of a nanomedicine. One possible set of tools for obtaining this information is molecular imaging. Molecular imaging is a field of research dedicated to the real time monitoring of biological processes in vivo, without the use of invasive techniques such as biopsies and dissections. Molecular imaging has been used extensively to follow the in vivo behaviour of a labelled material. This is advantageous because the performance of a single material in one subject can be monitored and mapped against the progression of disease. It can help to provide the pharmacokinetic information necessary for preclinical development of nanomedicines. Nanomedicines can be designed to combine molecular imaging with targeting molecules and therapeutic agents to create a theranostic, which can be used for simultaneous imaging and treatment of disease. This thesis aims to synthesise novel multimodal molecular imaging agents based on a hyperbranched polymer architecture, and to gain a deeper understanding of how these materials behave in vivo. To achieve this, biocompatible hyperbranched polymers with defined architectures were synthesised using RAFT polymerisation techniques. These materials were extensively characterised using a wide range of spectroscopic techniques to thoroughly understand their physical and chemical properties. A variety of synthetic strategies were investigated for functionalising both the α- and ω-chain ends of these polymers with multiple imaging ligands to form multimodal imaging agents. Far-red and near-infrared fluorophores provided for fluorescence imaging and radiometal chelators allowed for positron emission tomography (PET) imaging. These hyperbranched polymer systems were first evaluated as molecular imaging agents in C57 BL/6J mice using whole animal fluorescence and PET-CT imaging. It was shown that the rate of excretion was dependent on the size and level of branching of the hyperbranched polymer cores. The larger more highly branched material showed extended circulation times, making it suitable for use as a passive targeting agent for cancer. It was demonstrated in a murine model for melanoma, that the material showed significant uptake within the tumour after 24 hours and that the material was not cleared from the tissue within 72 hours. To gain a deeper understanding of the behaviour of these materials in vivo, PET imaging was combined with gadolinium contrast enhanced MRI, in order to gain both molecular and physiological information. Using this technique, we were able to show that while a folic acid targeted hyperbranched polymer did accumulate in the tumour tissue, its distribution was concentrated in highly vascularised areas of the tumour. This is the first time that this phenomenon has been demonstrated at a macroscopic level, in a living animal. This has important implications for using these materials as theranostics, because heterogeneous distribution of the nanomaterial, and therefore delivery of a therapeutic, can lead to ineffective treatment of the cancer and thus lead to tumour recurrence. In further development of these imaging agents into theranostics, targeting of the hyperbranched polymers by conjugating single chain fragment antibodies (scFv) was explored. Two potential routes to improve efficiency of conjugation were investigated. Both approaches used novel bifunctional oligoethylene glycol (OEG) linkers to introduce the required chemical functionality to either the hyperbranched polymer or scFv. The first approach utilised a heterobifunctional OEG which was synthesised with a pentafluorophenol ester at one end for coupling with amines and an ω-azide group at the other end to allow for the copper catalysed Huigsen 1,3-dipolar cycloaddition reactions. This linker was first attached to the scFv via activated ester chemistry, to provide the necessary azide functionality for coupling of the scFv to the alkyne end groups of the hyperbranched polymer. The second route used an enzymatic cross coupling approach using the sortase enzyme. In order to achieve this, a triglycine functionalised OEG ligand was synthesised and attached to the hyperbranched polymer. The triglycine could then be used as a substrate for enzymatic cross coupling to scFv bioengineered to possess the required recognition sequence (LPETG). Despite both OEG linkers being demonstrated to be able to undergo conjugation to both the hyperbranched polymers and scFv independently, further optimisation is required to achieve conjugation of the two macromolecules.
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Varpness, Zachary Bradley. "Biomimetic synthesis of catalytic materials." Diss., Montana State University, 2007. http://etd.lib.montana.edu/etd/2007/varpness/VarpnessZ0807.pdf.

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Andersson, Nina. "Mesostructured materials : Synthesis towards applications /." Stockholm : Department of Physical, Inorganic and Structural Chemistry, Stockholm university, 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-6584.

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Chirico, Pietro. "Synthesis of nanocrystalline nitride materials." Thesis, University of Southampton, 2011. https://eprints.soton.ac.uk/193141/.

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Gonzalez, Estefan Juan Héctor. "Microfluidic synthesis of switchable materials." Thesis, Bordeaux, 2019. http://www.theses.fr/2019BORD0199.

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La méthodologie classique pour la synthèse de matériaux à transition de spin a un certain degré d’irréproductibilité du fait de l’imprévisibilité des flux turbulents à l’intérieur du milieu réactionnel contenu dans la verrerie ordinaire de laboratoire. Pour tenter de résoudre ce problème, nous explorons la microfluidique de gouttelettes sans tensioactifs comme une nouvelle méthode d’obtention de matériaux à transition de spin.Après avoir testé divers dispositifs microfluidiques, nous avons synthétisé le MOF de type Hofmann [Fe(pz)Pt(CN)4] en combinant deux solutions de réactifs dans un canal débouchant immédiatement dans une buse de focalisation de flux. Le produit obtenu présente une réduction drastique de la taille de particule par rapport aux méthodes classiques, et affiche un comportement magnétique consistent avec les nanoparticules rapportées antérieurement.Malheureusement, du fait des hautes concentrations utilisées ici, la réaction se produit très rapidement, et le dispositif peut facilement se boucher si les flux sont modifiés ou perturbés. Pour résoudre ce problème, nous avons développé une nouvelle méthode : une substance causant un gonflement du PDMS est mélangée avec l’huile de la phase continue pour obtenir une réduction des dimensions du dispositive, et ainsi réduire le diamètre des gouttes de presque deux ordres de grandeur
The conventional methodology to synthesize spin-crossover materials has some degree of irreproducibility due to the unpredictability of the turbulent flows in the reaction media contained in ordinary laboratory glassware. To address this issue, we explore surfactant-free droplet microfluidics as a new method to synthesize spin-crossover materials.After probing the use of different microfluidic devices, we synthesized the Hofmann type MOF [Fe(pz)Pt(CN)4] by combining two solutions with reactants into a channel that immediately reaches a flow-focusing junction. The product obtained displays a strong decrease in its particle size compared with the batch synthesis. The obtained nanoparticles display a magnetic behavior consistent with the nanoparticles reported previously.Unfortunately, under the high concentrations used here, the reaction occurs very quickly, and the device can easily clog when the flow rates are changed. This leads to difficulties when attempting to modulate the dimensions of the droplets without affecting the general performance of the device. To solve this problem, we developed a new method where a swelling agent is combined with the oil used as the continuous phase, resulting in a change in the critical dimensions of the PDMS chip and a change of the diameter of the droplets of almost two orders of magnitude
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Wang, Jinfeng. "Characterization and synthesis of nanoscale materials." Diss., Rolla, Mo. : Missouri University of Science and Technology, 2008. http://scholarsmine.mst.edu/thesis/pdf/JinfengWang_09007dcc80564540.pdf.

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Thesis (Ph. D.)--Missouri University of Science and Technology and University of Missouri--St. Louis, 2008.
Vita. The entire thesis text is included in file. Title from title screen of thesis/dissertation PDF file (viewed August 28, 2008) Thesis completed as part of a cooperative degree program with Missouri University of Science & Technology and the University of Missouri--St. Louis. Includes bibliographical references (p. 129-142).
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Gosline, Andrew H. 1978. "Haptic synthesis of dynamically deformable materials." Thesis, McGill University, 2009. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=115667.

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Haptic simulation of medical procedures is an active area of research in engineering and medicine. Analogous to flight simulators for pilots, surgery simulators can allow medical students and doctors to practice procedures in a risk free and well monitored virtual environment. The quality of interaction that a surgery simulator can generate is dependent upon many components. In this thesis, careful attention is paid to the haptic display of viscous effects.
Viscous terms, defined here as terms that are dependent upon velocity, are typically computed 'using a discrete time backwards difference estimation of the velocity. It is well known that differentation has the tendency to amplify high frequency noise, and as a result, the backwards difference estimation generates considerable errors when applied to the quantized position readings from a digital encoder. Prior to this work, the only feasible method to improve velocity estimation was to use a variety of observation or filtering techniques, all of which inevitably add phase delay. In this thesis, the backwards difference operation was analyzed in detail. It was found that feedback viscosity simulation is very non-robust to noise, and oscillations exist in the presence of quantization noise regardless of the physical parameters of the plant.
A typical haptic interface for surgery simulation consists of a mechanical linkage driven by electric motors. These linkages are controlled with a computer using a discrete-time force update law that generates a prescribed force given the user's position in the medical virtual environment. It is clear from the literature that a haptic interface must have some level of physical dissipation to enable a passive rendering due to the inherent instability associated with time delayed systems. However, dissipation in typical haptic interfaces is a byproduct of their design, and is neither controllable nor easily identifiable. A prototype haptic interface is presented in this thesis that uses eddy current brakes to add high bandwidth programmable dissipation to an existing motor linkage. The new hardware has been optimized experimentally to maximize damping and minimize inertia given conventional machining and available material constraints.
A new paradigm in the control of haptic interfaces is time-domain passivity control. Passive systems are desirable in haptics because a passive system is globally stable, passivity theory applies to linear and nonlinear systems alike, and a user cannot extract energy from a passive system. Passivity controllers monitor the energy flow in the device and add virtual damping to remove any energy that violates the passivity constraint. Unfortunately, the amount of virtual damping available to a given device is limited by the physical dissipation that it exhibits. If the device is directly driven and light, such as the pantograph, the available virtual damping is insufficient to maintain the passivity constraint. The eddy current brakes allow programmable physical damping to be used in place of virtual damping which has been shown with experiments to improve the stable impedance range of a haptic interface.
It is clear from the literature that most tissues in a human body exhibit viscoelastic behavior. Simulation of viscoelastic objects requires that the velocity of interaction be known. Because typical haptic interfaces use digital encoders to sample position, the estimated velocity signal is noisy, delayed or both. Eddy current brakes are viscous actuators by nature, as they generate a resistive force proportional to the velocity. To take advantage of this fact, viscoelastic decomposition algorithms were developed that can output viscous components to the eddy current brakes and elastic components to the motors. This technique reduces or eliminates the use of a velocity estimation signal in the feedback loop which improves passivity, reduces motor saturation effects, and allows for a wider stable range of mechanical impedances than conventional haptic interfaces can achieve.
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Lees, Rachel Jane Elizabeth. "Solvothermal synthesis of novel inorganic materials." Thesis, Heriot-Watt University, 2007. http://hdl.handle.net/10399/2087.

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Solvothennal and hydrothennal synthesis is widely applied in the generation of . metastable crystalline phases, and is used in this work to prepare a range of novel antimony-sulphide and rare-earth oxy-anion compounds in' the presence of linear, branched and macrocycle amines. The new crystalline phases were characterised using single-crystal X-ray diffraction, elemental analysis, diffuse reflectance spectroscopy and SQUID magnetometry. Transition-metals included in the reactions resulted in the fonnation of both binary antimony-sulphide and ternary transition-metal-antimony-sulphide structures. Binary phases include [Fe(en)3]Sb2Ss.0.55H20, [Fe(en)3hSb4Sg, [T(dien)2]Sb6SIO.xH20 (T= Ni, Co), [Co(en)3]SbgS13 and tNi(en)3]Sb12S19, where discrete [Sb2Sst units, SbS2chains, Sb6SI0 6- and SbgS13 2- layers and a three-dimensional Sbl2Slt framework are charge balanced by transition-I.l1etal-amine complexes. The ternary phases synthesised using tris(2-aminoethyl)amine (tren) and diethylenetriamine (dien) include [Cr(tren)]Sb4S7 chains with [Cr(tren)f+ pendent complexes, and [T(dien)hSblgS30[ T(dien)2] (T= Mn, Fe, Co), in which complex antimony-sulphide chains are bridged via dimeric [T2S2] units to fonn novel layers. The transition-metal ions all exhibit paramagnet~c behaviour and the band gaps of the phases were found to increase from 1.79(4) to 2.46(1) eV with increasing framework density. The first examples of hydrothennal antimony-sulphide reactions using a macrocycle, cyclam, as the structure directing agent resulted in the synthesis of novel , layered and three-dimensional phases of[cyclarnH2]Sb6SIO and [cyclamH2]Sb4S7. By including transition-metal salts in the reaction mixture, it was possible to incorporate transition-metal ions within the macrocyclic rings in [Ni(cyclam)]Sb4S7 and [Co(cyclam)]x[cyclarnH2]J_xSb4S7, where the C02+ occupancy varies between O.08
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Penny, George B. S. "High-pressure synthesis of electronic materials." Thesis, University of Edinburgh, 2010. http://hdl.handle.net/1842/4161.

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High-pressure techniques have become increasingly important in the synthesis of ceramic and metallic solids allowing the discovery of new materials with interesting properties. In this research dense solid oxides have been synthesised at high pressures, and structural investigations have been conducted using x-ray and neutron diffraction. The perovskite LaPdO3 has been synthesised at pressures of 6{10GPa. Neutron diffraction studies have been carried out from 7{260K to investigate any structural distortions, particularly related to the possibility of charge order at low temperatures. No reduction in symmetry associated with charge ordering has been observed; the material appears to remain metallic with only one unique Pd site down to 7K. LaPdO3 adopts the GdFeO3-type Pbnm structure. The PdO6 octahedra exhibit a tetragonal distortion throughout the temperature range with a shortening of the apical Pd{O bonds of 2:5% relative to the equatorial bonds. Attempts to prepare analogues of the perovskite containing smaller rare earths have resulted in multi-phase samples, and further RPdO3 perovskites remain inaccessible although there is evidence for a small amount of the perovskite phase in the products of synthesis attempts with neodymium. Three new oxypnictide superconductors, RFeAsO1 xFx (R = Tb, Dy and Ho) have been synthesised at 7{12GPa. The materials are isostructural with other recently discovered iron arsenide superconductors and have Tc's of 52:8 K, 48:5K and 36:2K respectively, demonstrating a downturn in Tc in the series for smaller R. Systematic studies on TbFeAsO0.9F0.1 and HoFeAsO0.9F0.1 show negative values of dTc=dV in contrast to those reported for early R containing materials. Low-temperature neutron diffraction measurements on both materials, and synchrotron studies on HoFeAsO0.9F0.1 reveal no tetragonal to orthorhombic transitions as observed in early R-containing materials with lower doping levels. Magnetic reflections are evident but they are shown to be from R2O3 and RAs impurities with TN's of 5:5K for Tb2O3, 6:5K for HoAs and 1:7K < TN < 4K for Ho2O3. The implications of these results for superconductivity in the iron arsenides are discussed.
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Davies, Hazel M. "Synthesis and characterisation of molecular materials." Thesis, University of Bath, 2008. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501495.

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Chapter 1 contains a brief background into subjects such as Robin-Day classes, binary code, logic gates and electrochemistry in order to aid understanding of the rest of the chapter. The unique paradigm of Molecular Quantum Cellular Automata (MQCA) is presented along with the advantages it offers to traditional silicon based electronics. A summary of the existing modelled and synthesised MQCA systems is included along with an explanation of the characteristics required for materials to be suitable for MQCA. The subject of chapter 2 is cyclopentadiene cobalt cyclobutadiene complexes for the application of MQCA. The introduction examines the mechanism for the formation of cyclopentadiene cobalt cyclobutadiene complexes and the bonding in these compounds. A range of acetylenes were prepared for the formation of cyclopentadiene cobalt cyclobutadiene complexes were examined and characterised. Metal fragments including {Ru(dppe)2Cl} and AuPPh3Cl were attached to a cyclopentadiene cobalt cyclobutadiene core and these materials were characterised. The subject of chapter 3 is benzene based materials for the application of MQCA. 1,2,4,5-tetrakis(ferrocenylethynyl)benzene was prepared, characterised and the electrochemistry was examined for electronic communication between the ferrocene sites. A range of two metal centre compounds were examined for solubility and electrochemical stability with the view of preparing four metal centre compounds with a benzene core. The subject of chapter 4 is porphyrin based materials. This was the first area of work for this thesis and was discontinued. A brief summary of the synthetic work carried out is described, along with some literature work that was published whilst this work was being carried. Chapter 5 contains the experimental information for chapters 2-4.
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Books on the topic "030306 Synthesis of Materials"

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Winter, Charles H., and David M. Hoffman, eds. Inorganic Materials Synthesis. Washington, DC: American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-1999-0727.

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Nicola, Hüsing, ed. Synthesis of inorganic materials. 3rd ed. Weinheim: Wiley-VCH, 2012.

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Nicola, Hüsing, ed. Synthesis of inorganic materials. Weinheim: Wiley-VCH, 2000.

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1942-, Occelli Mario L., and Robson Harry E. 1927-, eds. Synthesis of microporous materials. New York: Van Nostrand Reinhold, 1992.

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L, Perry Dale, and American Chemical Society, eds. Materials synthesis and characterization. New York: Plenum Press, 1997.

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Perry, Dale L., ed. Materials Synthesis and Characterization. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-0145-3.

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Khina, B. B. Combustion synthesis of advanced materials. New York: Nova Science Publishers, 2010.

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Moore, John Jeremy. Synthesis and processing of materials. Birmingham: University of Birmingham, 1996.

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Hadjipanayis, George C. Nanophase Materials: Synthesis - Properties - Applications. Dordrecht: Springer Netherlands, 1994.

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Khina, B. B. Combustion synthesis of advanced materials. Hauppauge, N.Y: Nova Science Publishers, 2010.

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Book chapters on the topic "030306 Synthesis of Materials"

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Yahya, Noorhana, Poppy Puspitasari, Krzysztof Koziol, and Pavia Guiseppe. "Ammonia Synthesis." In Advanced Structured Materials, 395–413. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/8611_2010_25.

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Ramazani S.A., A., Y. Tamsilian, and M. Shaban. "Synthesis of Nanomaterials." In Nanocomposite Materials, 37–80. Taylor & Francis Group, 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742: CRC Press, 2016. http://dx.doi.org/10.1201/9781315372310-4.

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Nedoluzhko, Aleksey, and Trevor Douglas. "Biomimetic Materials Synthesis." In Physics and Chemistry Basis of Biotechnology, 9–45. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/0-306-46891-3_1.

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Fang, Zhen. "Other Materials Synthesis." In Rapid Production of Micro- and Nano-particles Using Supercritical Water, 63–69. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-12987-2_5.

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Venkateshalu, Sandhya, and Andrews Nirmala Grace. "Synthesis and Processing Strategies." In Engineering Materials, 17–36. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-05006-0_2.

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Moon, Geon Dae. "Synthesis and Assembly." In SpringerBriefs in Materials, 7–51. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-03943-1_2.

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Thompson, Derek P. "Mechanochemical Nitride Synthesis." In Materials Science Forum, 51–57. Stafa: Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-439-1.51.

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Klabunde, K. J., J. V. Stark, O. Koper, C. Mohs, A. Khaleel, G. Glavee, D. Zhang, C. M. Sorensen, and G. C. Hadjipanayis. "Chemical Synthesis of Nanophase Materials." In Nanophase Materials, 1–19. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1076-1_1.

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Sorensen, C. M., Q. Li, H. K. Xu, Z. X. Tang, K. J. Klabunde, and G. C. Hadjipanayis. "Aerosol Spray Pyrolysis Synthesis Techniques." In Nanophase Materials, 109–16. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1076-1_15.

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Deheri, Pratap Kumar, and Biswabandita Kar. "Synthesis of Nanoclay Composite Material." In Engineering Materials, 69–103. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-62761-4_4.

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Conference papers on the topic "030306 Synthesis of Materials"

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Zhang, Ying, Raffi Kamalian, Alice M. Agogino, and Carlo H. Sequin. "Hierarchical MEMS synthesis and optimization." In Smart Structures and Materials, edited by Vijay K. Varadan. SPIE, 2005. http://dx.doi.org/10.1117/12.600376.

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Alva, Shridhara, Jayant Kumar, Kenneth A. Marx, and Sukant K. Tripathy. "Biochemical synthesis of electroactive polymers." In Smart Materials, Structures and MEMS, edited by Vasu K. Aatre, Vijay K. Varadan, and Vasundara V. Varadan. SPIE, 1998. http://dx.doi.org/10.1117/12.305594.

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Panda, Maheswar, Venimadhav Adyam, V. Srinivas, A. K. Thakur, Amitabha Ghoshray, and Bilwadal Bandyopadhyay. "Synthesis And Characterization Of Ni-PVDF Nano-Composites." In MAGNETIC MATERIALS: International Conference on Magnetic Materials (ICMM-2007). AIP, 2008. http://dx.doi.org/10.1063/1.2928977.

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MOORE, JOHN. "Combustion synthesis of advanced composite materials." In 31st Aerospace Sciences Meeting. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1993. http://dx.doi.org/10.2514/6.1993-830.

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Maeda, Hirotaka, Emile Hideki Ishida, Fangming Jin, Qi Zhou, and Bing Wu. "Hydrothermal Synthesis of Humidity Controlling Materials." In 2nd International Symposium on Aqua Science, Water Resource and Low Carbon Energy. AIP, 2010. http://dx.doi.org/10.1063/1.3529298.

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Lu, L., Z. Jing, Z. Wang, X. Pan, E. H. Ishida, Fangming Jin, Qi Zhou, and Bing Wu. "Hydrothermal Synthesis of Loessial Mesoporous Materials." In 2nd International Symposium on Aqua Science, Water Resource and Low Carbon Energy. AIP, 2010. http://dx.doi.org/10.1063/1.3529308.

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Vailionis, Arturas, Eugene G. Gamaly, Vygantas Mizeikis, Wenge Yang, Andrei Rode, and Saulius Juodkazis. "Synthesis of Materials by Ultrafast Microexplosion." In CLEO: Science and Innovations. Washington, D.C.: OSA, 2011. http://dx.doi.org/10.1364/cleo_si.2011.cwo1.

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Tirumala, Vijaya Raghavan, Derrick C. Mancini, and Gerard T. Caneba. "Synthesis of ultrafast response smart microgel structures." In Smart Structures and Materials, edited by Vijay K. Varadan. SPIE, 2004. http://dx.doi.org/10.1117/12.543401.

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Chakane, Sanjay D. S., Shilpa Jain, and S. V. Bhoraskar. "Synthesis, characterization, and humidity sensing of metallophtalocyanines." In Smart Materials and MEMS, edited by Dinesh K. Sood, Ronald A. Lawes, and Vasundara V. Varadan. SPIE, 2001. http://dx.doi.org/10.1117/12.420871.

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Siewierski, Lisa M., Lorraine M. Lander, Andrea Liebmann, William J. Brittain, and Mark D. Foster. "Synthesis and characterization of a photoactive monolayer." In Smart Structures & Materials '95, edited by A. Peter Jardine. SPIE, 1995. http://dx.doi.org/10.1117/12.209788.

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Reports on the topic "030306 Synthesis of Materials"

1

Morkoc, Hadis. Synthesis of Multifunctional Materials. Fort Belvoir, VA: Defense Technical Information Center, September 2006. http://dx.doi.org/10.21236/ada459645.

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Willson, C. G. Shock compression synthesis of hard materials. Office of Scientific and Technical Information (OSTI), March 1999. http://dx.doi.org/10.2172/334297.

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Deevi, S. C., and V. K. Sikka. Reaction synthesis of heat-resistant materials. Office of Scientific and Technical Information (OSTI), December 1995. http://dx.doi.org/10.2172/273757.

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Greenawald, E., W. Bailey, E. Bellinger, K. Campbell, and Y. S. Ham. Synthesis and Characterization of Advanced Materials. Fort Belvoir, VA: Defense Technical Information Center, April 2001. http://dx.doi.org/10.21236/ada389684.

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O'Connor, Charles J. Nanophase Synthesis of Magnetic Materials: Thick Film Ferrite Magnetic Materials. Fort Belvoir, VA: Defense Technical Information Center, February 1998. http://dx.doi.org/10.21236/ada349674.

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Petrovic, J. J., R. G. Castro, and D. P. Butt. Synthesis and design of silicide intermetallic materials. Office of Scientific and Technical Information (OSTI), April 1997. http://dx.doi.org/10.2172/494111.

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De Yoreo, J., C. Orme, P. Dove, and H. Teng. Physical basis for materials synthesis using biomineralization. Office of Scientific and Technical Information (OSTI), May 2000. http://dx.doi.org/10.2172/15005096.

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He, Lin. Synthesis, characterization and application of electrode materials. Office of Scientific and Technical Information (OSTI), July 1995. http://dx.doi.org/10.2172/108148.

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Miller, Joel S. SYNTHESIS of MOLECULE/POLYMER-BASED MAGNETIC MATERIALS. Office of Scientific and Technical Information (OSTI), February 2016. http://dx.doi.org/10.2172/1236463.

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Graham, David E., Ji-Won Moon, Beth L. Armstrong, Panos G. Datskos, Chad E. Duty, Ryan Gresback, Ilia N. Ivanov, et al. Manufacturing Demonstration Facility: Low Temperature Materials Synthesis. Office of Scientific and Technical Information (OSTI), June 2015. http://dx.doi.org/10.2172/1261265.

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