Relevant bibliographies by topics / Nanostructured materials. Polymer melting

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Nanostructured materials. Polymer melting'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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Journal articles on the topic "Nanostructured materials. Polymer melting"

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Mohlala, M. Sarah, and Suprakas Sinha Ray. "Preparation and Characterization of Polymer/Multi-Walled Carbon Nanotube Nanocomposites." Solid State Phenomena 140 (October 2008): 97–102. http://dx.doi.org/10.4028/www.scientific.net/ssp.140.97.

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This paper describes the preparation, characterization and properties of nanostructured composite materials based on poly(butylene adipate-co-polycaprolactam) (PBA-co-PCL)/multiwalled carbon nanotubes (MWCNTs) and polycaprolactone (PCL)/MWCNTs. The polymer/MWCNTs nanocomposites were prepared by mixing the polymers with various amounts of MWCNTs using both solution and melt blending processes. The dispersion of MWCNTs into the polymer matrix was analyzed by transmission electron microscopy (TEM) and the thermal stability of the nanocomposites was studied by thermal gravimetric analysis (TGA). Differential scanning calorimetry (DSC) was used to study the crystallization and melting behaviour of the polymer matrices containing the MWCNTs.
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THOMPSON, S., N. K. DUTTA, and N. ROY CHOUDHURY. "APPLICATION OF MICROTHERMAL ANALYSIS AND PULSED FORCE MICROSCOPY TO CHARACTERIZE NANOSTRUCTURED POLYMER." International Journal of Nanoscience 03, no. 06 (December 2004): 839–43. http://dx.doi.org/10.1142/s0219581x04002735.

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In this investigation, we present the first results of Microthermal analysis (MicroTA) and Pulsed-Force-Mode (PFM) scanning force microscopy employed for visualization and characterization of nanostructured side-chain crystalline polymeric material. PFM was employed to clearly visualize the interesting self-organizing characteristics and the intimate contact of crystalline order as well as amorphous disorder in such polymer. As the sample was heated above the melting point, the well-defined crystalline regions observed at lower temperature no longer exist, and diffused melt boundaries are clearly observed using PFM. The nanophase separated system undergoes a sharp change in its adhesion and stiffness properties with temperature below and above the crystal melting point. Local thermal analyses using MicroTA exhibit consistent rapid crystal melting curves and its lateral homogeneity.
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Dencheva, Nadya, Maria Jovita Oliveira, Olga S. Carneiro, Teresa G. Nunes, and Zlatan Z. Denchev. "Preparation and Properties of Novel In Situ Composite Materials Based on Polyethylene-Polyamide Oriented Blends." Materials Science Forum 587-588 (June 2008): 515–19. http://dx.doi.org/10.4028/www.scientific.net/msf.587-588.515.

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The objective of this study is to manufacture and investigate novel nanostructured polymer composites (NPC) based on oriented blends of high-density polyethylene (HDPE) and polyamide 6 (PA6). Conventional polymer processing techniques are used for this purpose including extrusion blending, cold drawing and compression molding. Thus, various polymer blends are prepared comprising 10 and 20 wt% of PA6 and 0-10 wt% of a copolymeric compatibilizer. These blends are cold-drawn to high draw ratios and the oriented strands so produced are further compression molded at various temperatures between the melting points of HDPE and PA6. All NPC obtained are characterized by microscopy techniques, solid state NMR, mechanical tests and wide- and small-angle X-ray scattering from synchrotron. The mechanical and structural data of NPCs are discussed with relation with the polyamide fibrils’ orientation, as well as with the effect of compatibilizer at the matrix-fibrils interface.
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Kaewsichan, Lupong, Jasadee Kaewsrichan, and Thitima Chuchom. "Nanostructured Polycaprolactone-Inorganic Phosphate Hybrid Scaffold for Medical Applications." Advanced Materials Research 93-94 (January 2010): 67–70. http://dx.doi.org/10.4028/www.scientific.net/amr.93-94.67.

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New hybrid macroporous scaffolds of polycaprolactone (PCL)/tricalcium phosphate (TCP) were developed by taking into account mechanical properties of the bone to be replaced. FTIR spectra indicated the coating of TCP onto the polymer, providing hydrophilic surfaces necessary for cells to attach. As determined by DSC, the depression of PCL melting point suggested a uniform distribution of PCL within the TCP matrix. SEM micrographs revealed pores of irregular shapes varying from 100-200 µm in size in the resultant structures. Indeed, the pore morphology was precisely determined by the leached particles. The scaffolds could tolerate the impact of at least 5.6 kNm2, making them suitable for use as artificial bones of skull, clavicle and ribs. Rat bone stroma attached and survived on the scaffolds, indicating biocompatible of the used materials. Therefore, the prepared scaffolds would be applicable for bone tissue engineering in the near future.
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Ponomarenko, O., A. Y. Nikulin, H. O. Moser, P. Yang, and O. Sakata. "Radiation-induced melting in coherent X-ray diffractive imaging at the nanoscale." Journal of Synchrotron Radiation 18, no. 4 (May 26, 2011): 580–94. http://dx.doi.org/10.1107/s0909049511016335.

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Coherent X-ray diffraction techniques play an increasingly significant role in the imaging of nanoscale structures, ranging from metallic and semiconductor to biological objects. In material science, X-rays are usually considered to be of a low-destructive nature, but under certain conditions they can cause significant radiation damage and heat loading on the samples. The qualitative literature data concerning the tolerance of nanostructured samples to synchrotron radiation in coherent diffraction imaging experiments are scarce. In this work the experimental evidence of a complete destruction of polymer and gold nanosamples by the synchrotron beam is reported in the case of imaging at 1–10 nm spatial resolution. Numerical simulations based on a heat-transfer model demonstrate the high sensitivity of temperature distribution in samples to macroscopic experimental parameters such as the conduction properties of materials, radiation heat transfer and convection. However, for realistic experimental conditions the calculated rates of temperature rise alone cannot explain the melting transitions observed in the nanosamples. Comparison of these results with the literature data allows a specific scenario of the sample destruction in each particular case to be presented, and a strategy for damage reduction to be proposed.
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Xu, Xianlin, Gaokao Zhang, Shubo Wang, Shengnan Lv, and Xupin Zhuang. "Fabrication of fibrous microfiltration membrane by pore filling of nanofibers into poly(ethylene terephthalate) nonwoven scaffold." Journal of Industrial Textiles 50, no. 4 (March 21, 2019): 566–83. http://dx.doi.org/10.1177/1528083719837733.

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A nanofibrous microfiltration membrane with high flux, low pressure drop, and high retention capacity was fabricated by pore filling of copolyetherester nanofibers (low-melting-point polyester; melting point of 110℃) into a poly(ethylene terephthalate) nonwoven scaffold. Short low-melting-point polyester nanofibers were anchored on the surface of the poly(ethylene terephthalate) fibers by heat treatment to form a crosslinked nanostructured mesh with very high porosity and high specific surface area. The pore size and distribution of the membranes can be adjusted by varying the loading amount of nanofibers. The resulting membrane not only possessed good interception ability for 5, 3, and 1.3 µm polystyrene microspheres but also exhibited desirable water permeability. In the circulating filtration test, with the accumulation of membrane fouling in the filtration, the membrane was also effective in retaining particulate matter while improving the antipollution ability. These properties are desirable for the effective removal of pollutants on the membrane and restoration of the membrane flux.
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Savchuk, Andriy I., Volodymyr I. Fediv, Tetyana A. Savchuk, Ihor D. Stolyarchuk, Yevheniy O. Kandyba, Dmytro I. Ostafiychuk, Svitlana A. Ivanchak, and Vitaliy V. Makoviy. "Optical and Magneto-Optical Studies of Composite Materials Containing Semimagnetic Semiconductor Nanoparticles." Solid State Phenomena 151 (April 2009): 259–63. http://dx.doi.org/10.4028/www.scientific.net/ssp.151.259.

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Сomposite films containing II-VI based semiconductor nanoparticles have been prepared by different physical and chemical techniques. Non-magnetic CdS1-xSex nanoparticles were grown by melting of the semiconductor doped fine powder borosilicate glass. The composite semimagnetic semiconductor Cd1-xMnxTe based films were fabricated by embedding in SiO2 matrix with using of pulsed laser deposition technique. New chemical approach to synthesis of Cd1-xMnxS nanoparticles in polymer matrix has been proposed. The optical absorption edge for CdS1-xSex , Cd1-xMnxTe nanoparticles and exciton structure in the spectrum of Cd1-xMnxS nanoparticles shifted to the higher-energy side compared to those for bulk crystals due to the quantum confinement effect. Magneto-optical Faraday effect for non-magnetic semiconductor nanoparticles in glass demonstrates only small changes as compared with that of bulk semiconductors. The revealed peculiarities in spectral and magnetic field dependences of the Faraday rotation for the studied semimagnetic semiconductor composite films can be attributed to the influence of dimensionality on spin exchange parameters for such kind of nanostructures.
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Vannikov, A. V., A. D. Grishina, and E. I. Maltsev. "Nanostructured polymer materials and polymer-based devices." Nanotechnologies in Russia 4, no. 1-2 (February 2009): 1–18. http://dx.doi.org/10.1134/s1995078009010017.

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Nanda, Karuna Kar. "Anomaly in Thermal Stability of Nanostructured Materials." Materials Science Forum 653 (June 2010): 23–30. http://dx.doi.org/10.4028/www.scientific.net/msf.653.23.

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Understanding of the melting temperature of nanostructures is beneficial to exploit phase transitions and their applications at elevated temperatures. The melting temperature of nanostructured materials depends on particle size, shape and dimensionality and has been well established both experimentally and theoretically. The large surface-to-volume ratio is the key for the low melting temperature of nanostructured materials. The melting temperature of almost free nanoparticles decreases with decreasing size although there are anomalies for some cases. Superheating has been reported for some embedded nanoparticles. Local maxima and minima in the melting temperature have been reported for particles with fewer atoms. Another quantity that is influenced by large surface-to-volume ratio and related to the thermal stability, is the vapour pressure. The vapour pressure of nanoparticles is shown to be enhanced for smaller particles. In this article, we have discussed the anomaly in thermal stability of nanostructured materials.
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Hu, Zhibing. "Nanostructured polymer gels." Macromolecular Symposia 207, no. 1 (February 2004): 47–56. http://dx.doi.org/10.1002/masy.200450305.

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Dissertations / Theses on the topic "Nanostructured materials. Polymer melting"

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Tang, Shijun. "Characterization, Properties and Applications of Novel Nanostructured Hydrogels." Thesis, University of North Texas, 2006. https://digital.library.unt.edu/ark:/67531/metadc5605/.

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The characterization, properties and applications of the novel nanostructured microgel (nanoparticle network and microgel crystal) composed of poly-N-isopropylacrylanmide-co-allylamine (PNIPAM-co-allylamine) and PNIPAM-co-acrylic acid(AA) have been investigated. For the novel nanostructured hydrogels with the two levels of structure: the primary network inside each individual particle and the secondary network of the crosslinked nanoparticles, the new shear modulus, drug release law from hydrogel with heterogeneous structure have been studied. The successful method for calculating the volume fraction related the phase transition of colloid have been obtained. The kinetics of crystallization in an aqueous dispersion of PNIPAM particles has been explored using UV-visible transmission spectroscopy. This dissertation also includes the initial research on the melting behavior of colloidal crystals composed of PNIPAM microgels. Many new findings in this study area have never been reported before. The theoretical model for the columnar crystal growth from the top to bottom of PNIPAM microgel has been built, which explains the growth mechanism of the novel columnar hydrogel colloidal crystals. Since the unique structure of the novel nanostructured hydrogels, their properties are different with the conventional hydrogels and the hard-sphere-like system. The studies and results in this dissertation have the important significant for theoretical study and valuable application of these novel nanostructured hydrogels.
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Farghaly, Ahmed A. "Fabrication of Multifunctional Nanostructured Porous Materials." VCU Scholars Compass, 2016. http://scholarscompass.vcu.edu/etd/4189.

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Nanostructured porous materials generally, and nanoporous noble metals specifically, have received considerable attention due to their superior chemical and physical properties over nanoparticles and bulk counterparts. This dissertation work aims to develop well-established strategies for the preparation of multifunctional nanostructured porous materials based on the combination of inorganic-chemistry, organic-chemistry and electrochemistry. The preparation strategies involved one or more of the following processes: sol-gel synthesis, co-electrodeposition, metal ions reduction, electropolymerization and dealloying or chemical etching. The study did not stop at the preparation limits but extended to investigate the reaction mechanism behind the formation of these multifunctional nanoporous structures in order to determine the different factors controlling the nanoporous structures formation. First, gold-silica nanocomposites were prepared and used as a building blocks for the fabrication of high surface area gold coral electrodes. Well-controlled surface area enhancement, film thickness and morphology were achieved. An enhancement in the electrode’s surface area up to 57 times relative to the geometric area was achieved. A critical sol-gel monomer concentration was also noted at which the deposited silica around the gold coral was able to stabilize the gold corals and below which the deposited coral structures are not stable. Second, free-standing and transferable strata-like 3D porous polypyrrole nanostructures were obtained from chemical etching of the electrodeposited polypyrrole-silica nanocomposite films. A new reaction mechanism was developed and a new structural directing factor has been discovered for the first time. Finally, silver-rich platinum alloys were prepared and dealloyed in acidic medium to produce 3D bicontinuous nanoporous platinum nanorods and films with a nanoporous gold-like structure. The 3D-BC-NP-Pt displayed high surface area, typical electrochemical sensing properties in an aqueous medium, and exceptional electrochemical sensing capability in a complex biofouling environment containing fibrinogen. The 3D-BC-NP-Pt displayed high catalytic activity toward the methanol electro-oxidation that is 30 times higher that of planar platinum and high volumetric capacitance of 400 F/cm3. These findings will pave the way toward the development of high performance and reliable electrodes for catalysis, sensing, high power outputs fuel cells, battery-like supercapacitors and miniaturized device applications.
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GUO, QINGYUN. "GIANT MOLECULE BASED NANOSTRUCTURED MATERIALS: FROM STRUCTURE TO FUNCTIONALITY." University of Akron / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=akron1603757858889563.

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Li, Jing. "Electrical conducting polymer nanocomposites containing graphite nanoplatelets and carbon nanotubes /." View abstract or full-text, 2006. http://library.ust.hk/cgi/db/thesis.pl?MECH%202006%20LI.

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Cheung, Man Kuen. "Investigating the tribological performance of different polymer and polymer nanocomposites using nanoscratch and wear techniques /." access full-text access abstract and table of contents, 2005. http://libweb.cityu.edu.hk/cgi-bin/ezdb/thesis.pl?mphil-ap-b19887772a.pdf.

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Thesis (M.Phil.)--City University of Hong Kong, 2005.
"Submitted to Department of Physics and Materials Science in partial fulfillment of the requirements for the degree of Master of Philosophy" Includes bibliographical references (leaves 82-95)
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Gandhi, Sahil Sandesh. "NANOSTRUCTURED OPTICAL MATERIALS BASED ON LIQUID CRYSTAL AND POLYMER COMPOSITES." Kent State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=kent151074495757849.

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Kuryak, Chris A. (Chris Adam). "Nanostructured thin film thermoelectric composite materials using conductive polymer PEDOT:PSS." Thesis, Massachusetts Institute of Technology, 2013. http://hdl.handle.net/1721.1/79270.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2013.
Cataloged from PDF version of thesis.
Includes bibliographical references (p. 65).
Thermoelectric materials have the ability to convert heat directly into electricity. This clean energy technology has advantages over other renewable technologies in that it requires no sunlight, has no moving parts, and is easily scalable. With the majority of the unused energy in the United States being wasted in the form of heat and the recent mandates to reduce greenhouse gas emissions, thermoelectric devices could play an important role in our energy future by recovering this wasted heat and increasing the efficiency of energy production. However, low conversion efficiencies and the high cost of crystalline thermoelectric materials have restricted their implementation into modem society. To combat these issues, composite materials that use conductive polymers have been under investigation due to their low cost, manufacturability, and malleability. These new composite materials could lead to cheaper thermoelectric devices and even introduce the technology to new application areas. Unfortunately, polymer composites have been plagued by low operating efficiencies due to their low Seebeck coefficient. In this research, we show an enhanced Seebeck coefficient at the interface of poly(3,4- ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) spin coated onto silicon substrates. The maximum Seebeck coefficient achieved was 473 uV/K with a PEDOT:PSS thickness of 7.75 nm. Furthermore, the power factor of this interface was optimized with a 15.25 nm PEDOT:PSS thickness to a value of 1.24 uV/K2-cm, which is an order of magnitude larger than PEDOT:PSS itself. The effect of PEDOT:PSS thickness and silicon thickness on the thermoelectric properties is also discussed. Continuing research into this area will attempt to enhance the power factor even further by investigating better sample preparation techniques that avoid silicon surface oxidation, as well as creating a flexible composite material of PEDOT:PSS with silicon nanowires..
by Chris A. Kuryak.
S.M.
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Brown, Elvie Escorro. "Bacterial cellulose/thermoplastic polymer nanocomposites." Online access for everyone, 2007. http://www.dissertations.wsu.edu/Thesis/Spring2007/e_brown_050207.pdf.

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Ratnagiri, Ramabhadra 1972. "Investigation of mixing in the melting regime during polymer compounding." Thesis, Massachusetts Institute of Technology, 1999. http://hdl.handle.net/1721.1/9131.

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Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, February 2000.
Includes bibliographical references (leaves 124-126).
Morphology evolution in the melting regime during compounding of immiscible polymer blends. where most of the size scale reduction occurs. is studied. Starting from an initial solid pellet mixture of two components. the progression to the final two-phase viscoelastic melt involves an intermediate stage where either one or both the components are melting or softening. Our focus is identifying and quantifying the factors that determine morphologies in the melting regime. We identify blend systems that exhibit a transformation in morphology from a minor-component continuous phase with dispersed major component domains to that with the major component being the continuous matrix phase. as a function of mixing time. This phenomenon of phase inversion during compounding is demonstrated to occur even in blends with a higher melting point minor component. A low solid modulus and a low melt viscosity are shown to favor the formation of the continuous phase by the minor component. Polycaprolactone/polyethylene. polystyrene/polyethylene. polycarbonate/ polyethylene, poly(ethylene-co-cyclohexane dimethylene terephthalate)/ polyethylene. and polybutylene/polycaprolactone blends were studied. These model blends were chosen based on the melt viscosity ratio and the relative softening temperatures of the two components. These two parameters were used to develop a two-dimensional framework for summarizing the compounding behavior of blends. For compounding runs with a small amount of the minor component (-1 Owt. % ) at a constant mixer temperature, phase inversion was observed for blend viscosity ratios less than 0.2. irrespective of the relative transition temperatures of the two components. Using a temperature ramping program resulted in the low melting component forming the continuous phase initially. Selective dissolution studies were used to quantify the amount of minor component present in the continuous phase at different mixing times. A polystyrene/polyethylene blend with a melt viscosity ratio of -0.001. was used to study the effect of batch size on the time required to form a continuous phase of the compounding of batch sizes ranging from 12g to 240g. Upon a five-fold increase in batch size the time to phase inversion increased by a factor of 3. This increase was explained by a combination of reduced heat conduction and reduced mechanical energy input to the batch. To enable studies at different batch sizes in the same mixing bowl, a novel mixing blade with modular elements was designed and constructed. This design was used for both radial and axial scaleup studies. The effect of changing the blade configuration on the time to phase inversion was explained using a specific relative stagger parameter, which is a measure of the effectiveness of stress transfer to the batch. Flow visualization using a glass window and blend sampling was used to develop a detailed description of the deformation steps leading to phase inversion in a model low viscosity ratio blend. Intermediate morphologies of flattened pellets, stacks of pellets, fibers and clusters were identified. Based on these observations a micro-structural model was developed to predict the time to phase inversion. The model incorporates a simplified flow-field approximation and calculates the strain in the major component. A strain-based criterion was proposed which in conjunction with the model yielded an explicit expression for the time to phase inversion. Model predictions of the dependence of time to phase inversion on nominal maximum-shear-rate in the mixer, volume fraction of the minor component and blend viscosity ratio were shown to be in excellent agreement with experimental results.
by Ramabhadra Ratnagiri.
Ph.D.
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Tang, Youhong. "Microrheological study on polyethylene/thermotropic liquid crystalline polymer/layered silicates nanocomposites /." View abstract or full-text, 2007. http://library.ust.hk/cgi/db/thesis.pl?CENG%202007%20TANG.

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Books on the topic "Nanostructured materials. Polymer melting"

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Misra, Devesh K. Polymer nanocomposites. Warrendale, Pa: Minerals, Metals and Materials Society, 2006.

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Nanotechnology and polymer-based nanostructures. New York: Nova Science Publishers, 2011.

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1952-, Russell Thomas P., ed. Polymer thin films. Hackensack, N.J: World Scientific, 2008.

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Ke, Y. C. Polymer-layered silicate and silica nanocomposites. Boston, Mass: Elsevier, 2005.

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Nelson, J. Keith. Dielectric polymer nanocomposites. New York: Springer, 2010.

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Ray, Suprakas Sinha. Environmentally friendly polymer nanocomposites: Types, processing and properties. Oxford, UK: Woodhead Publishing, 2013.

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Vilgis, T. A. Reinforcement of polymer nano-composites. Cambridge: Cambride University Press, 2009.

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Advances in polymer nanocomposites: Types and applications. Cambridge: Woodhead, 2012.

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Mittal, Vikas. In-situ synthesis of polymer nanocomposites. Weinheim: Wiley-VCH, 2011.

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Seimitsu kōbunshi no kiso to jitsuyōka gijutsu: Fundamental and practical technologies for nano-structured polymeric materials. Tōkyō-to Chiyoda-ku: Shīemushī Shuppan, 2014.

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Book chapters on the topic "Nanostructured materials. Polymer melting"

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Du, Jianzhong. "Polymer Vesicles." In Advanced Hierarchical Nanostructured Materials, 177–92. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664948.ch5.

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Andrievski, R. A. "The-State-of-the-Art of Nanostructured High Melting Point Compound-Based Materials." In Nanostructured Materials, 263–82. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5002-6_13.

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Toshima, Naoki. "Polymer-capped Bimetallic Nanoclusters as Active and Selective Catalysts." In Macromolecular Nanostructured Materials, 182–96. Berlin, Heidelberg: Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-08439-7_11.

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Pailleret, Alain, and Oleg Semenikhin. "Nanoscale Inhomogeneity of Conducting-Polymer-Based Materials." In Nanostructured Conductive Polymers, 99–159. Chichester, UK: John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470661338.ch3.

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Chen, Hsien-Yeh, Chiao-Tzu Su, and Meng-Yu Tsai. "Nanoscale Functional Polymer Coatings for Biointerface Engineering." In Advanced Hierarchical Nanostructured Materials, 461–78. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527664948.ch13.

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Mayeen, Anshida, and Nandakumar Kalarikkal. "Piezoelectric Polymer Nanocomposites For Energy Scavenging Applications." In Polymeric and Nanostructured Materials, 273–92. Oakville, ON ; Waretown, NJ : Apple Academic Press, 2019. |: Apple Academic Press, 2018. http://dx.doi.org/10.1201/b22428-18.

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Gupta, Sanjeev K., Mina Talati, and Prafulla K. Jha. "Shape and Size Dependent Melting Point Temperature of Nanoparticles." In Metastable and Nanostructured Materials III, 132–37. Stafa: Trans Tech Publications Ltd., 2008. http://dx.doi.org/10.4028/0-87849-474-x.132.

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Yuvashree, S., and J. Balavijayalakshmi. "Metal Oxide Embellished on Polymer Functionalized Reduced Graphene Oxide for Electrochemical Detection of Hydrogen Peroxide." In Nanostructured Smart Materials, 1–11. First edition.: Apple Academic Press, 2021. http://dx.doi.org/10.1201/9781003130468-1.

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Ramalakshmi, V., and J. Balavijayalakshmi. "Polymer Functionalized Reduced Graphene Oxide-Based Nickel Nanoparticles as Highly Efficient Dye Catalyst for Water Remediation." In Nanostructured Smart Materials, 61–75. First edition.: Apple Academic Press, 2021. http://dx.doi.org/10.1201/9781003130468-4.

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Pavlidis, Ioannis V., Aikaterini A. Tzialla, Apostolos Enotiadis, Haralambos Stamatis, and Dimitrios Gournis. "Enzyme Immobilization on Layered and Nanostructured Materials." In Biocatalysis in Polymer Chemistry, 35–63. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527632534.ch2.

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Conference papers on the topic "Nanostructured materials. Polymer melting"

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Koo, Joseph, Louis Pilato, and Gerry Wissler. "Polymer Nanostructured Materials for Propulsion Systems." In 41st AIAA/ASME/SAE/ASEE Joint Propulsion Conference & Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2005. http://dx.doi.org/10.2514/6.2005-3606.

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Althaus, Jasmin, Prabitha Urwyler, Celestino Padeste, Roman Heuberger, Hans Deyhle, Helmut Schift, Jens Gobrecht, et al. "Micro- and nanostructured polymer substrates for biomedical applications." In SPIE Smart Structures and Materials + Nondestructive Evaluation and Health Monitoring, edited by Akhlesh Lakhtakia. SPIE, 2012. http://dx.doi.org/10.1117/12.915235.

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Wudy, K., D. Drummer, and M. Drexler. "Characterization of polymer materials and powders for selective laser melting." In PROCEEDINGS OF PPS-29: The 29th International Conference of the Polymer Processing Society - Conference Papers. American Institute of Physics, 2014. http://dx.doi.org/10.1063/1.4873875.

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Constantopoulos, Kristina T., Cameron J. Shearer, Joseph G. Shapter, Nicolas H. Voelcker, and Amanda V. Ellis. "Preparation and characterization of multiwalled carbon nanotube (MWCNT)/polymer nanostructured materials." In Smart Materials, Nano-and Micro-Smart Systems, edited by Nicolas H. Voelcker and Helmut W. Thissen. SPIE, 2008. http://dx.doi.org/10.1117/12.810958.

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Olson, Jeremy D., Glenn P. Gray, and Sue A. Carter. "Optimizing Hybrid Nanocrystal/Polymer Photovoltaics Through Ligand Choice." In Solar Energy: New Materials and Nanostructured Devices for High Efficiency. Washington, D.C.: OSA, 2008. http://dx.doi.org/10.1364/solar.2008.swa2.

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Polkehn, Matthias, Pierre Eisenbrandt, Hiroyuki Tamura, Stefan Haacke, Stéphane Méry, and Irene Burghardt. "Ultrafast excitonic and charge transfer dynamics in nanostructured organic polymer materials." In SPIE Photonics Europe, edited by David L. Andrews, Jean-Michel Nunzi, and Andreas Ostendorf. SPIE, 2016. http://dx.doi.org/10.1117/12.2230314.

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Su, Wei-Hsiang, and Ching-Fuh Lin. "Enhanced efficiency of polymer photovoltaic devices by using silicon nanowires." In Solar Energy: New Materials and Nanostructured Devices for High Efficiency. Washington, D.C.: OSA, 2008. http://dx.doi.org/10.1364/solar.2008.stuc9.

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Clancy, Thomas, Sarah-Jane Frankland, and Jeffrey Hinkley. "Prediction of Material Properties of Nanostructured Polymer Composites Using Atomistic Simulations." In 50th AIAA/ASME/ASCE/AHS/ASC Structures, Structural Dynamics, and Materials Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2009. http://dx.doi.org/10.2514/6.2009-2385.

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Tsigara, A., L. Athanasekos, A. Meristoudi, J. Manasis, M. Hands, G. Mousdis, S. Pispas, and N. A. Vainos. "Inorganic and hybrid polymer-inorganic nanostructured materials for optical physicochemical sensing applications." In SPIE Proceedings, edited by Valentin I. Vlad. SPIE, 2007. http://dx.doi.org/10.1117/12.757862.

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Donsì, Francesco, Simonetta Bartolucci, Paolo Bettotti, Federico Carosio, Patrizia Contursi, Gennaro Gentile, Marina Scarpa, and Giorgia Spigno. "A Technology Platform For the Sustainable Recovery and Advanced Use of Nanostructured Cellulose from Agri-Food Residues (PANACEA Project)." In The First International Conference on “Green” Polymer Materials 2020. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/cgpm2020-07212.

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