17 pages, 1868 KiB  
Review
Liquid Crystal Microlenses for Autostereoscopic Displays
by José Francisco Algorri *, Virginia Urruchi, Braulio García-Cámara and José M. Sánchez-Pena
Electronic Technology Department, Carlos III University of Madrid, Avenida de la Universidad 30, Leganés E28911, Spain
Materials 2016, 9(1), 36; https://doi.org/10.3390/ma9010036 - 11 Jan 2016
Cited by 33 | Viewed by 8690
Abstract
Three-dimensional vision has acquired great importance in the audiovisual industry in the past ten years. Despite this, the first generation of autostereoscopic displays failed to generate enough consumer excitement. Some reasons are little 3D content and performance issues. For this reason, an exponential [...] Read more.
Three-dimensional vision has acquired great importance in the audiovisual industry in the past ten years. Despite this, the first generation of autostereoscopic displays failed to generate enough consumer excitement. Some reasons are little 3D content and performance issues. For this reason, an exponential increase in three-dimensional vision research has occurred in the last few years. In this review, a study of the historical impact of the most important technologies has been performed. This study is carried out in terms of research manuscripts per year. The results reveal that research on spatial multiplexing technique is increasing considerably and today is the most studied. For this reason, the state of the art of this technique is presented. The use of microlenses seems to be the most successful method to obtain autostereoscopic vision. When they are fabricated with liquid crystal materials, extended capabilities are produced. Among the numerous techniques for manufacturing liquid crystal microlenses, this review covers the most viable designs for its use in autostereoscopic displays. For this reason, some of the most important topologies and their relation with autostereoscopic displays are presented. Finally, the challenges in some recent applications, such as portable devices, and the future of three-dimensional displays based on liquid crystal microlenses are outlined. Full article
(This article belongs to the Special Issue Materials for Display Applications)
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13 pages, 3590 KiB  
Article
Heteroatom Doped-Carbon Nanospheres as Anodes in Lithium Ion Batteries
by George S. Pappas 1,†, Stefania Ferrari 1,*,†, Xiaobin Huang 2, Rohit Bhagat 1, David M. Haddleton 3 and Chaoying Wan 1,*
1 Warwick Manufacturing Group, University of Warwick, Coventry CV4 7AL, UK
2 School of Aeronautics and Astronautics, Shanghai Jiao Tong University, Shanghai 200240, China
3 Department of Chemistry, University of Warwick, Coventry CV4 7AL, UK
These authors contributed equally to this work.
Materials 2016, 9(1), 35; https://doi.org/10.3390/ma9010035 - 9 Jan 2016
Cited by 38 | Viewed by 8943
Abstract
Long cycle performance is a crucial requirement in energy storage devices. New formulations and/or improvement of “conventional” materials have been investigated in order to achieve this target. Here we explore the performance of a novel type of carbon nanospheres (CNSs) with three heteroatom [...] Read more.
Long cycle performance is a crucial requirement in energy storage devices. New formulations and/or improvement of “conventional” materials have been investigated in order to achieve this target. Here we explore the performance of a novel type of carbon nanospheres (CNSs) with three heteroatom co-doped (nitrogen, phosphorous and sulfur) and high specific surface area as anode materials for lithium ion batteries. The CNSs were obtained from carbonization of highly-crosslinked organo (phosphazene) nanospheres (OPZs) of 300 nm diameter. The OPZs were synthesized via a single and facile step of polycondensation reaction between hexachlorocyclotriphosphazene (HCCP) and 4,4′-sulphonyldiphenol (BPS). The X-ray Photoelectron Spectroscopy (XPS) analysis showed a high heteroatom-doping content in the structure of CNSs while the textural evaluation from the N2 sorption isotherms revealed the presence of micro- and mesopores and a high specific surface area of 875 m2/g. The CNSs anode showed remarkable stability and coulombic efficiency in a long charge–discharge cycling up to 1000 cycles at 1C rate, delivering about 130 mA·h·g−1. This study represents a step toward smart engineering of inexpensive materials with practical applications for energy devices. Full article
(This article belongs to the Special Issue Electrode Materials)
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16 pages, 7362 KiB  
Article
Aminopropyl-Silica Hybrid Particles as Supports for Humic Acids Immobilization
by Mónika Sándor 1, Cristina Lavinia Nistor 2,*, Gábor Szalontai 3, Rusandica Stoica 2, Cristian Andi Nicolae 2, Elvira Alexandrescu 2, József Fazakas 1, Florin Oancea 2 and Dan Donescu 2
1 Faculty of Chemistry and Chemical Engineering, Babes-Bolyai University, Arany János Street, No.11, Cluj-Napoca 400028, Romania
2 National Research & Development Institute for Chemistry and Petrochemistry—ICECHIM, Splaiul Independentei No.202, 6th district, PO Box 35-174, Bucharest 060021, Romania
3 NMR Laboratory, Institute of Materials Engineering, University of Pannonia, Egyetem Street, No. 10, Veszprém 8200, Hungary
Materials 2016, 9(1), 34; https://doi.org/10.3390/ma9010034 - 8 Jan 2016
Cited by 26 | Viewed by 8931
Abstract
A series of aminopropyl-functionalized silica nanoparticles were prepared through a basic two step sol-gel process in water. Prior to being aminopropyl-functionalized, silica particles with an average diameter of 549 nm were prepared from tetraethyl orthosilicate (TEOS), using a Stöber method. In a second [...] Read more.
A series of aminopropyl-functionalized silica nanoparticles were prepared through a basic two step sol-gel process in water. Prior to being aminopropyl-functionalized, silica particles with an average diameter of 549 nm were prepared from tetraethyl orthosilicate (TEOS), using a Stöber method. In a second step, aminopropyl-silica particles were prepared by silanization with 3-aminopropyltriethoxysilane (APTES), added drop by drop to the sol-gel mixture. The synthesized amino-functionalized silica particles are intended to be used as supports for immobilization of humic acids (HA), through electrostatic bonds. Furthermore, by inserting beside APTES, unhydrolysable mono-, di- or trifunctional alkylsilanes (methyltriethoxy silane (MeTES), trimethylethoxysilane (Me3ES), diethoxydimethylsilane (Me2DES) and 1,2-bis(triethoxysilyl)ethane (BETES)) onto silica particles surface, the spacing of the free amino groups was intended in order to facilitate their interaction with HA large molecules. Two sorts of HA were used for evaluating the immobilization capacity of the novel aminosilane supports. The results proved the efficient functionalization of silica nanoparticles with amino groups and showed that the immobilization of the two tested types of humic acid substances was well achieved for all the TEOS/APTES = 20/1 (molar ratio) silica hybrids having or not having the amino functions spaced by alkyl groups. It was shown that the density of aminopropyl functions is low enough at this low APTES fraction and do not require a further spacing by alkyl groups. Moreover, all the hybrids having negative zeta potential values exhibited low interaction with HA molecules. Full article
(This article belongs to the Section Advanced Materials Characterization)
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16 pages, 1391 KiB  
Article
A Critical Evaluation of the Influence of the Dark Exchange Current on the Performance of Dye-Sensitized Solar Cells
by Rodrigo García-Rodríguez 1,*, Julio Villanueva-Cab 2, Juan A. Anta 3 and Gerko Oskam 1,*
1 Departamento de Física Aplicada, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional (CINVESTAV-IPN), Mérida, Yucatán 97310, Mexico
2 Instituto de Física, Benemérita Universidad Autónoma de Puebla (BUAP), Puebla, Puebla 72570, Mexico
3 Nanostructured Solar Cells Group, Department of Physical, Chemical and Natural Systems, Universidad Pablo de Olavide, Seville ES-41013, Spain
Materials 2016, 9(1), 33; https://doi.org/10.3390/ma9010033 - 8 Jan 2016
Cited by 8 | Viewed by 6428
Abstract
The influence of the thickness of the nanostructured, mesoporous TiO2 film on several parameters determining the performance of a dye-sensitized solar cell is investigated both experimentally and theoretically. We pay special attention to the effect of the exchange current density in the [...] Read more.
The influence of the thickness of the nanostructured, mesoporous TiO2 film on several parameters determining the performance of a dye-sensitized solar cell is investigated both experimentally and theoretically. We pay special attention to the effect of the exchange current density in the dark, and we compare the values obtained by steady state measurements with values extracted from small perturbation techniques. We also evaluate the influence of exchange current density, the solar cell ideality factor, and the effective absorption coefficient of the cell on the optimal film thickness. The results show that the exchange current density in the dark is proportional to the TiO2 film thickness, however, the effective absorption coefficient is the parameter that ultimately defines the ideal thickness. We illustrate the importance of the exchange current density in the dark on the determination of the current–voltage characteristics and we show how an important improvement of the cell performance can be achieved by decreasing values of the total series resistance and the exchange current density in the dark. Full article
(This article belongs to the Special Issue Electrode Materials)
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13 pages, 2717 KiB  
Article
Buckling Behavior of Substrate Supported Graphene Sheets
by Kuijian Yang 1, Yuli Chen 1,*, Fei Pan 1, Shengtao Wang 1, Yong Ma 1 and Qijun Liu 2
1 Institute of Solid Mechanics, International Research Institute for Multidisciplinary Science, Beihang University, Beijing 100191, China
2 Department of Aerospace Engineering, University of Illinois, Champaign, IL 61801, USA
Materials 2016, 9(1), 32; https://doi.org/10.3390/ma9010032 - 7 Jan 2016
Cited by 41 | Viewed by 6923
Abstract
The buckling of graphene sheets on substrates can significantly degrade their performance in materials and devices. Therefore, a systematic investigation on the buckling behavior of monolayer graphene sheet/substrate systems is carried out in this paper by both molecular mechanics simulations and theoretical analysis. [...] Read more.
The buckling of graphene sheets on substrates can significantly degrade their performance in materials and devices. Therefore, a systematic investigation on the buckling behavior of monolayer graphene sheet/substrate systems is carried out in this paper by both molecular mechanics simulations and theoretical analysis. From 70 simulation cases of simple-supported graphene sheets with different sizes under uniaxial compression, two different buckling modes are investigated and revealed to be dominated by the graphene size. Especially, for graphene sheets with length larger than 3 nm and width larger than 1.1 nm, the buckling mode depends only on the length/width ratio. Besides, it is revealed that the existence of graphene substrate can increase the critical buckling stress and strain to 4.39 N/m and 1.58%, respectively, which are about 10 times those for free-standing graphene sheets. Moreover, for graphene sheets with common size (longer than 20 nm), both theoretical and simulation results show that the critical buckling stress and strain are dominated only by the adhesive interactions with substrate and independent of the graphene size. Results in this work provide valuable insight and guidelines for the design and application of graphene-derived materials and nano-electromechanical systems. Full article
(This article belongs to the Special Issue Graphene)
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12 pages, 1832 KiB  
Article
Improved Electrochemical Detection of Zinc Ions Using Electrode Modified with Electrochemically Reduced Graphene Oxide
by Jiri Kudr 1,2, Lukas Richtera 1,2, Lukas Nejdl 1,2, Kledi Xhaxhiu 1,2, Petr Vitek 3, Branislav Rutkay-Nedecky 1,2, David Hynek 1,2, Pavel Kopel 1,2, Vojtech Adam 1,2 and Rene Kizek 4,*
1 Department of Chemistry and Biochemistry, Mendel University in Brno, Zemedelska 1, Brno CZ-613 00, Czech Republic
2 Central European Institute of Technology, Brno University of Technology, Technicka 3058/10, Brno CZ-616 00, Czech Republic
3 Global Change Research Institute, The Czech Academy of Sciences, v.v.i., Bělidla 4a, Brno CZ-603 00, Czech Republic
4 Department of Biomedical and Environmental Analysis, Wroclaw Medical University, Borowska 211, Wrocław PL-50 556, Poland
Materials 2016, 9(1), 31; https://doi.org/10.3390/ma9010031 - 7 Jan 2016
Cited by 41 | Viewed by 8849
Abstract
Increasing urbanization and industrialization lead to the release of metals into the biosphere, which has become a serious issue for public health. In this paper, the direct electrochemical reduction of zinc ions is studied using electrochemically reduced graphene oxide (ERGO) modified glassy carbon [...] Read more.
Increasing urbanization and industrialization lead to the release of metals into the biosphere, which has become a serious issue for public health. In this paper, the direct electrochemical reduction of zinc ions is studied using electrochemically reduced graphene oxide (ERGO) modified glassy carbon electrode (GCE). The graphene oxide (GO) was fabricated using modified Hummers method and was electrochemically reduced on the surface of GCE by performing cyclic voltammograms from 0 to −1.5 V. The modification was optimized and properties of electrodes were determined using electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The determination of Zn(II) was performed using differential pulse voltammetry technique, platinum wire as a counter electrode, and Ag/AgCl/3 M KCl reference electrode. Compared to the bare GCE the modified GCE/ERGO shows three times better electrocatalytic activity towards zinc ions, with an increase of reduction current along with a negative shift of reduction potential. Using GCE/ERGO detection limit 5 ng·mL−1 was obtained. Full article
(This article belongs to the Section Advanced Materials Characterization)
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13 pages, 6106 KiB  
Article
Facile Synthesis of SrCO3-Sr(OH)2/PPy Nanocomposite with Enhanced Photocatalytic Activity under Visible Light
by Alfredo Márquez-Herrera 1,*, Victor Manuel Ovando-Medina 2, Blanca Estela Castillo-Reyes 2, Martin Zapata-Torres 3, Miguel Meléndez-Lira 4 and Jaquelina González-Castañeda 5
1 Departamento de Ingeniería Agrícola, DICIVA, Campus Irapuato-Salamanca, Universidad de Guanajuato, Ex Hacienda el Copal, Carr. Irapuato-Silao km 9, Irapuato Gto 36500, Mexico
2 Ingeniería Química, COARA, Universidad Autónoma de San Luis Potosí, Carr. a Cedral Km 5+600, San José de las Trojes, Matehuala, San Luis Potosí 78700, Mexico
3 Centro de Investigación en Ciencia Aplicada y Tecnología Avanzada, Unidad Legaría IPN, Calzada Legaría 694, Col. Irrigación, México D.F. 11500, Mexico
4 Departamento de Física, CINVESTAV-IPN, Apartado Postal 14-740, México D.F. 07000, Mexico
5 Departamento de Ingeniería Ambiental, DICIVA, Campus Irapuato-Salamanca, Universidad de Guanajuato, Ex Hacienda el Copal, Carr. Irapuato-Silao km 9, Irapuato Gto 36500, Mexico
Materials 2016, 9(1), 30; https://doi.org/10.3390/ma9010030 - 6 Jan 2016
Cited by 38 | Viewed by 10097
Abstract
Pyrrole monomer was chemically polymerized onto SrCO3-Sr(OH)2 powders to obtain SrCO3-Sr(OH)2/polypyrrole nanocomposite to be used as a candidate for photocatalytic degradation of methylene blue dye (MB). The material was characterized by Fourier transform infrared (FTIR) spectroscopy, [...] Read more.
Pyrrole monomer was chemically polymerized onto SrCO3-Sr(OH)2 powders to obtain SrCO3-Sr(OH)2/polypyrrole nanocomposite to be used as a candidate for photocatalytic degradation of methylene blue dye (MB). The material was characterized by Fourier transform infrared (FTIR) spectroscopy, UV/Vis spectroscopy, and X-ray diffraction (XRD). It was observed from transmission electronic microscopy (TEM) analysis that the reported synthesis route allows the production of SrCO3-Sr(OH)2 nanoparticles with particle size below 100 nm which were embedded within a semiconducting polypyrrole matrix (PPy). The SrCO3-Sr(OH)2 and SrCO3-Sr(OH)2/PPy nanocomposites were tested in the photodegradation of MB dye under visible light irradiation. Also, the effects of MB dye initial concentration and the catalyst load on photodegradation efficiency were studied and discussed. Under the same conditions, the efficiency of photodegradation of MB employing the SrCO3-Sr(OH)2/PPy nanocomposite increases as compared with that obtained employing the SrCO3-Sr(OH)2 nanocomposite. Full article
(This article belongs to the Special Issue Advancement of Photocatalytic Materials 2016)
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14 pages, 1857 KiB  
Article
Triggered Release from Thermoresponsive Polymersomes with Superparamagnetic Membranes
by Oliver Bixner 1,2, Steffen Kurzhals 1, Mudassar Virk 1 and Erik Reimhult 1,*
1 Institute for Biologically Inspired Materials, Department of Nanobiotechnology, University of Natural Resources and Life Sciences, Vienna, Muthgasse 11, Vienna 1190, Austria
2 School of Materials Science and Engineering, Centre for Biomimetic Sensor Science, Nanyang Technological University, 50 Nanyang Drive, 637553 Singapore
Materials 2016, 9(1), 29; https://doi.org/10.3390/ma9010029 - 6 Jan 2016
Cited by 29 | Viewed by 7473
Abstract
Magnetic polymersomes were prepared by self-assembly of the amphiphilic block copolymer poly(isoprene-b-N-isopropylacrylamide) with monodisperse hydrophobic superparamagnetic iron oxide nanoparticles (SPION). The specifically designed thermoresponsive block copolymer allowed for efficient incorporation of the hydrophobic nanoparticles in the membrane core and [...] Read more.
Magnetic polymersomes were prepared by self-assembly of the amphiphilic block copolymer poly(isoprene-b-N-isopropylacrylamide) with monodisperse hydrophobic superparamagnetic iron oxide nanoparticles (SPION). The specifically designed thermoresponsive block copolymer allowed for efficient incorporation of the hydrophobic nanoparticles in the membrane core and encapsulation of the water soluble dye calcein in the lumen of the vesicles. Magnetic heating of the embedded SPIONs led to increased bilayer permeability through dehydration of the thermoresponsive PNIPAM block. The entrapped calcein could therefore be released in controlled doses solely through exposure to pulses of an alternating magnetic field. This hybrid SPION-polymersome system demonstrates a possible direction for release applications that merges rational polymersome design with addressed external magnetic field-triggered release through embedded nanomaterials. Full article
(This article belongs to the Section Advanced Composites)
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13 pages, 1303 KiB  
Article
Poly-γ-Glutamic Acid: Biodegradable Polymer for Potential Protection of Beneficial Viruses
by Ibrahim R. Khalil 1,2,*, Victor U. Irorere 1, Iza Radecka 1, Alan T. H. Burns 1, Marek Kowalczuk 1,3, Jessica L. Mason 1 and Martin P. Khechara 1,*
1 Faculty of Science and Engineering, University of Wolverhampton, Wulfruna Street, Wolverhampton WV1 1LY, UK
2 Department of Biology, College of Science, Tikrit University, Tikrit PO Box 42, Iraq
3 Center of Polymer and Carbon Materials, Polish Academy of Sciences, ul. M. Curie-Skłodowskiej 34, Zabrze 41-819, Poland
Materials 2016, 9(1), 28; https://doi.org/10.3390/ma9010028 - 6 Jan 2016
Cited by 28 | Viewed by 9851
Abstract
Poly-γ-glutamic acid (γ-PGA) is a naturally occurring polymer, which due to its biodegradable, non-toxic and non-immunogenic properties has been used successfully in the food, medical and wastewater industries. A major hurdle in bacteriophage application is the inability of phage to persist for extended [...] Read more.
Poly-γ-glutamic acid (γ-PGA) is a naturally occurring polymer, which due to its biodegradable, non-toxic and non-immunogenic properties has been used successfully in the food, medical and wastewater industries. A major hurdle in bacteriophage application is the inability of phage to persist for extended periods in the environment due to their susceptibility to environmental factors such as temperature, sunlight, desiccation and irradiation. Thus, the aim of this study was to protect useful phage from the harmful effect of these environmental factors using the γ-PGA biodegradable polymer. In addition, the association between γ-PGA and phage was investigated. Formulated phage (with 1% γ-PGA) and non-formulated phage were exposed to 50 °C. A clear difference was noticed as viability of non-formulated phage was reduced to 21% at log10 1.3 PFU/mL, while phage formulated with γ-PGA was 84% at log10 5.2 PFU/mL after 24 h of exposure. In addition, formulated phage remained viable at log10 2.5 PFU/mL even after 24 h of exposure at pH 3 solution. In contrast, non-formulated phages were totally inactivated after the same time of exposure. In addition, non-formulated phages when exposed to UV irradiation died within 10 min. In contrast also phages formulated with 1% γ-PGA had a viability of log10 4.1 PFU/mL at the same exposure time. Microscopy showed a clear interaction between γ-PGA and phages. In conclusion, the results suggest that γ-PGA has an unique protective effect on phage particles. Full article
(This article belongs to the Special Issue Biodegradable and Bio-Based Polymers)
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19 pages, 611 KiB  
Article
A Comparison of Simple Methods to Incorporate Material Temperature Dependency in the Green’s Function Method for Estimating Transient Thermal Stresses in Thick-Walled Power Plant Components
by James Rouse *,† and Christopher Hyde
1 Department of Mechanical, Materials and Manufacturing Engineering, University of Nottingham, Nottingham, Nottinghamshire NG7 2RD, UK
These authors contributed equally to this work.
Materials 2016, 9(1), 26; https://doi.org/10.3390/ma9010026 - 6 Jan 2016
Cited by 8 | Viewed by 6601
Abstract
The threat of thermal fatigue is an increasing concern for thermal power plant operators due to the increasing tendency to adopt “two-shifting” operating procedures. Thermal plants are likely to remain part of the energy portfolio for the foreseeable future and are under societal [...] Read more.
The threat of thermal fatigue is an increasing concern for thermal power plant operators due to the increasing tendency to adopt “two-shifting” operating procedures. Thermal plants are likely to remain part of the energy portfolio for the foreseeable future and are under societal pressures to generate in a highly flexible and efficient manner. The Green’s function method offers a flexible approach to determine reference elastic solutions for transient thermal stress problems. In order to simplify integration, it is often assumed that Green’s functions (derived from finite element unit temperature step solutions) are temperature independent (this is not the case due to the temperature dependency of material parameters). The present work offers a simple method to approximate a material’s temperature dependency using multiple reference unit solutions and an interpolation procedure. Thermal stress histories are predicted and compared for realistic temperature cycles using distinct techniques. The proposed interpolation method generally performs as well as (if not better) than the optimum single Green’s function or the previously-suggested weighting function technique (particularly for large temperature increments). Coefficients of determination are typically above 0 . 96 , and peak stress differences between true and predicted datasets are always less than 10 MPa. Full article
(This article belongs to the Special Issue Failure Analysis in Materials)
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13 pages, 5066 KiB  
Article
Development of a Hopkinson Bar Apparatus for Testing Soft Materials: Application to a Closed-Cell Aluminum Foam
by Marco Peroni 1,*, George Solomos 1 and Norbert Babcsan 2
1 European Commission Joint Research Centre (JRC), IPSC, ELSA, Via E. Fermi 2749, Ispra (VA) 21027, Italy
2 Aluinvent Zrt., Ipari Park, Szeles utca 2, Felsőzsolca H-3561, Hungary
Materials 2016, 9(1), 27; https://doi.org/10.3390/ma9010027 - 5 Jan 2016
Cited by 16 | Viewed by 7118
Abstract
An increasing interest in lightweight metallic foams for automotive, aerospace, and other applications has been observed in recent years. This is mainly due to the weight reduction that can be achieved using foams and for their mechanical energy absorption and acoustic damping capabilities. [...] Read more.
An increasing interest in lightweight metallic foams for automotive, aerospace, and other applications has been observed in recent years. This is mainly due to the weight reduction that can be achieved using foams and for their mechanical energy absorption and acoustic damping capabilities. An accurate knowledge of the mechanical behavior of these materials, especially under dynamic loadings, is thus necessary. Unfortunately, metal foams and in general “soft” materials exhibit a series of peculiarities that make difficult the adoption of standard testing techniques for their high strain-rate characterization. This paper presents an innovative apparatus, where high strain-rate tests of metal foams or other soft materials can be performed by exploiting the operating principle of the Hopkinson bar methods. Using the pre-stress method to generate directly a long compression pulse (compared with traditional SHPB), a displacement of about 20 mm can be applied to the specimen with a single propagating wave, suitable for evaluating the whole stress-strain curve of medium-sized cell foams (pores of about 1–2 mm). The potential of this testing rig is shown in the characterization of a closed-cell aluminum foam, where all the above features are amply demonstrated. Full article
(This article belongs to the Special Issue Metal Foams: Synthesis, Characterization and Applications)
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12 pages, 3577 KiB  
Article
Enhanced Physicochemical and Biological Properties of Ion-Implanted Titanium Using Electron Cyclotron Resonance Ion Sources
by Csaba Hegedűs 1, Chia-Che Ho 2, Attila Csik 3, Sándor Biri 3,* and Shinn-Jyh Ding 2,4,*
1 Department of Biomaterials and Prosthetic Dentistry, University of Debrecen, Nagyerdei krt. 98, H-4032 Debrecen, Hungary
2 Institute of Oral Science, Chung Shan Medical University, Taichung City 402, Taiwan
3 Institute for Nuclear Research (ATOMKI), Hungarian Academy of Sciences, Bem tér 18/c, H-4026 Debrecen, Hungary
4 Department of Dentistry, Chung Shan Medical University Hospital, Taichung City 402, Taiwan
Materials 2016, 9(1), 25; https://doi.org/10.3390/ma9010025 - 4 Jan 2016
Cited by 17 | Viewed by 5962
Abstract
The surface properties of metallic implants play an important role in their clinical success. Improving upon the inherent shortcomings of Ti implants, such as poor bioactivity, is imperative for achieving clinical use. In this study, we have developed a Ti implant modified with [...] Read more.
The surface properties of metallic implants play an important role in their clinical success. Improving upon the inherent shortcomings of Ti implants, such as poor bioactivity, is imperative for achieving clinical use. In this study, we have developed a Ti implant modified with Ca or dual Ca + Si ions on the surface using an electron cyclotron resonance ion source (ECRIS). The physicochemical and biological properties of ion-implanted Ti surfaces were analyzed using various analytical techniques, such as surface analyses, potentiodynamic polarization and cell culture. Experimental results indicated that a rough morphology was observed on the Ti substrate surface modified by ECRIS plasma ions. The in vitro electrochemical measurement results also indicated that the Ca + Si ion-implanted surface had a more beneficial and desired behavior than the pristine Ti substrate. Compared to the pristine Ti substrate, all ion-implanted samples had a lower hemolysis ratio. MG63 cells cultured on the high Ca and dual Ca + Si ion-implanted surfaces revealed significantly greater cell viability in comparison to the pristine Ti substrate. In conclusion, surface modification by electron cyclotron resonance Ca and Si ion sources could be an effective method for Ti implants. Full article
(This article belongs to the Section Advanced Materials Characterization)
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11 pages, 2523 KiB  
Article
Preparation and Characterization of Inorganic PCM Microcapsules by Fluidized Bed Method
by Svetlana Ushak 1,2,*,†, M. Judith Cruz 1,†, Luisa F. Cabeza 3,† and Mario Grágeda 1,2,†
1 Department of Chemical Engineering and Mineral Processing and Center for Advanced Study of Lithium and Industrial Minerals (CELiMIN), University of Antofagasta, Av. Universidad de Antofagasta 02800, Campus Coloso, Antofagasta 127300, Chile
2 Solar Energy Research Center (SERC-Chile), Av Tupper 2007, Piso 4, Santiago 8370451, Chile
3 GREA Innovació Concurrent, Edifici CREA, Universitat de Lleida, Pere de Cabrera s/n, Lleida 25001, Spain
These authors contributed equally to this work.
Materials 2016, 9(1), 24; https://doi.org/10.3390/ma9010024 - 4 Jan 2016
Cited by 43 | Viewed by 11273
Abstract
The literature shows that inorganic phase change materials (PCM) have been very seldom microencapsulated, so this study aims to contribute to filling this research gap. Bischofite, a by-product from the non-metallic industry identified as having good potential to be used as inorganic PCM, [...] Read more.
The literature shows that inorganic phase change materials (PCM) have been very seldom microencapsulated, so this study aims to contribute to filling this research gap. Bischofite, a by-product from the non-metallic industry identified as having good potential to be used as inorganic PCM, was microencapsulated by means of a fluidized bed method with acrylic as polymer and chloroform as solvent, after compatibility studies of both several solvents and several polymers. The formation of bischofite and pure MgCl2·6H2O microcapsules was investigated and analyzed. Results showed an efficiency in microencapsulation of 95% could be achieved when using 2 min of fluidization time and 2 kg/h of atomization flow. The final microcapsules had excellent melting temperatures and enthalpy compared to the original PCM, 104.6 °C and 95 J/g for bischofite, and 95.3 and 118.3 for MgCl2·6H2O. Full article
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22 pages, 7516 KiB  
Article
Cutting Modeling of Hybrid CFRP/Ti Composite with Induced Damage Analysis
by Jinyang Xu * and Mohamed El Mansori
MSMP—EA 7350 Laboratoire, Arts et Métiers ParisTech, Rue Saint Dominique B.P. 508, 51006 Châlons-en-Champagne, France
Materials 2016, 9(1), 22; https://doi.org/10.3390/ma9010022 - 4 Jan 2016
Cited by 27 | Viewed by 8302
Abstract
In hybrid carbon fiber reinforced polymer (CFRP)/Ti machining, the bi-material interface is the weakest region vulnerable to severe damage formation when the tool cutting from one phase to another phase and vice versa. The interface delamination as well as the composite-phase damage [...] Read more.
In hybrid carbon fiber reinforced polymer (CFRP)/Ti machining, the bi-material interface is the weakest region vulnerable to severe damage formation when the tool cutting from one phase to another phase and vice versa. The interface delamination as well as the composite-phase damage is the most serious failure dominating the bi-material machining. In this paper, an original finite element (FE) model was developed to inspect the key mechanisms governing the induced damage formation when cutting this multi-phase material. The hybrid composite model was constructed by establishing three disparate physical constituents, i.e., the Ti phase, the interface, and the CFRP phase. Different constitutive laws and damage criteria were implemented to build up the entire cutting behavior of the bi-material system. The developed orthogonal cutting (OC) model aims to characterize the dynamic mechanisms of interface delamination formation and the affected interface zone (AIZ). Special focus was made on the quantitative analyses of the parametric effects on the interface delamination and composite-phase damage. The numerical results highlighted the pivotal role of AIZ in affecting the formation of interface delamination, and the significant impacts of feed rate and cutting speed on delamination extent and fiber/matrix failure. Full article
(This article belongs to the Section Manufacturing Processes and Systems)
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9 pages, 1461 KiB  
Article
Optical and Magneto-Optical Properties of Gd22Fe78 Thin Films in the Photon Energy Range From 1.5 to 5.5 eV
by Eva Jesenská 1,2,*, Takahiro Hashinaka 1, Takayuki Ishibashi 1, Lukáš Beran 2, Ján Dušek 2, Roman Antoš 2, Kiyoshi Kuga 3, Ken-ichi Aoshima 3, Kenji Machida 3, Hidekazu Kinjo 3 and Martin Veis 2,*
1 Department of Materials Science and Technology, Nagaoka University of Technology, Nagaoka, Niigata 1603-1, Japan
2 Institute of Physics, Charles University, Prague 12116, Czech Republic
3 Science and Technology Research Laboratories, Japan Broadcasting Corporation (NHK), Tokyo 157-8510, Japan
Materials 2016, 9(1), 23; https://doi.org/10.3390/ma9010023 - 2 Jan 2016
Cited by 8 | Viewed by 5503
Abstract
Optical and magneto-optical properties of amorphous Gd22Fe78 (GdFe) thin films prepared by direct current (DC) sputtering on thermally oxidized substrates were characterized by the combination of spectroscopic ellipsometry and magneto-optical spectroscopy in the photon energy range from 1.5 to 5.5 [...] Read more.
Optical and magneto-optical properties of amorphous Gd22Fe78 (GdFe) thin films prepared by direct current (DC) sputtering on thermally oxidized substrates were characterized by the combination of spectroscopic ellipsometry and magneto-optical spectroscopy in the photon energy range from 1.5 to 5.5 eV. Thin SiNx and Ru coatings were used to prevent the GdFe surface oxidation and contamination. Using advanced theoretical models spectral dependence of the complete permittivity tensor and spectral dependence of the absorption coefficient were deduced from experimental data. No significant changes in the optical properties upon different coatings were observed, indicating reliability of used analysis. Full article
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