Browsing by Subject "Manganese"

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Open Access
Compositional homogeneity in a medical-grade stainless steel sintered with a Mn-Si additive
(Elsevier, 2012-06-09) Salahinejad, E.; Hadianfard, M.J.; Ghaffari, M.; Mashhadi, S.B.; Okyay, Ali Kemal
In this paper, chemical composition uniformity in amorphous/ nanocrystallization medical-grade stainless steel (ASTM ID: F2581) sintered with a Mn-Si additive was studied via scanning electron microscopy, energy dispersive X-ray spectroscopy, and transmission electron microscopy. The results show that as a result of sintering at 1000 °C, no dissociation of Mn-Si additive particles embedded in the stainless steel matrix occurs. In contrast, sintering at 1050 °C develops a relatively homogeneous microstructure from the chemical composition viewpoint. The aforementioned phenomena are explained by liquation of the Mn-Si eutectic additive, thereby wetting of the main powder particles, penetrating into the particle contacts and pore zones via capillary forces, and providing a path of high diffusivity.
Open Access
Differences in the accumulation and distribution profile of heavy metals and metalloid between male and female crayfish (Astacus leptodactylus)
(2013) Tunca, E.; Ucuncu, E.; Ozkan, A.D.; Ulger, Z.E.; Cansizoǧlu, A.E.; Tekinay, T.
Concentrations of selected heavy metals and a metalloid were measured by ICP-MS in crayfish (Astacus leptodactylus) collected from Lake Hirfanli, Turkey. Aluminum (Al), chromium (52Cr, 53Cr), copper ( 63Cu, 65Cu), manganese (Mn), nickel (Ni) and arsenic (As) were measured in the exoskeleton, gills, hepatopancreas and abdominal muscle tissues of 60 crayfish of both genders. With the exception of Al, differences were determined between male and female cohorts for the accumulation trends of the above-mentioned elements in the four tissues. It was also noted that the accumulation rates of Ni and As were significantly lower in gill tissue of females compared to males and no significant difference was observed for Cu isotopes in female crayfish. Cluster Analysis (CA) recovered similar results for both genders, with links between accumulations of Ni and As being notable. Accumulation models were described separately for male and female crayfish using regression analysis, and are presented for models where R2 > 0.85. © 2013 Springer Science+Business Media New York.
Open Access
Fabrication of nanostructured medical-grade stainless steel by mechanical alloying and subsequent liquid-phase sintering
(Springer, 2012-05-10) Salahinejad, E.; Hadianfard, M. J.; Ghaffari, Mohammad; Mashhadi, S. B.; Okyay, Ali Kemal
This article focuses on the microstructure of medical-grade P558 (ASTM F2581) stainless steel produced by mechanical alloying and liquid-phase sintering. Rietveld X-ray diffraction and transmission electron microscopy reflect that the mechanically alloyed stainless steel powder is a nanocrystal dispersed amorphous matrix composite.Mn-11.5 wt pct Si eutectic alloy as additive improves densification of the synthesized P558 alloy via liquid-phase sintering mechanism. X-ray mapping shows that after sintering at 1323 K (105°C) for 1 hour, a uniform distribution of dissolved Mn and Si is achieved. Moreover, the development of a nanostructured, fully austenitic stainless steel after sintering at the same temperature is realized by X-ray diffraction and transmission electron microscopy.
Open Access
Fast and quick degradation properties of doped and capped ZnO nanoparticles under UV-Visible light radiations
(Elsevier Ltd, 2016) Mittal, M.; Sharma, M.; Pandey, O. P.
Undoped and Manganese (Mn) doped zinc oxide (ZnO) (Zn1- xMnxO, x=0.005, 0.01, 0.015 and 0.02) nanoparticles (NPs) capped with (1.0%) Thioglycerol (TG) has been successfully synthesized by co-precipitation method. Optical and morphological studies have been done for photophysical and structural analysis of synthesized materials. The photocatalytic activity of undoped and Mn doped ZnO NPs were investigated by degradation of crystal violet (CV) dye under UV-Visible light radiations. It has been found that Mn (1.0%) doping concentration is optimal for photophysical and photocatalytic properties. When the pH of as synthesized optimum doped ZnO NPs varied from natural pH i.e. from 6.7 to 8.0 and 10.0, the degradation of CV dye increases from 92% to 95% and 98% in 180min respectively. Further on increasing the pH of optimum doped synthesized NPs to 12.0, almost 100% degradation has been achieved in 150min. Optimum doped photocatalyst synthesized at pH-12.0 has also effectively degraded the CV dye solution in acidic and basic medium thus showed its utility in various industries. However, it has been found that 100% of CV dye quickly degraded in 30min when only 1.0% of hydrogen peroxide (H2O2) was introduced along with optimized NPs synthesized at pH-12. Kinetic studies show that the degradation of CV dye follows pseudo first and second-order kinetic law. Further an industrial anionic polyazo Sirius red F3B (SRF3B) dye has been degraded to 100% with optimized NPs synthesized at pH-12.0 in 15min only.
Open Access
Liquid-phase sintering of medical-grade P558 stainless steel using a new biocompatible eutectic additive
(Elsevier, 2012-02-02) Salahinejad, E.; Hadianfard, M. J.; Ghaffari, M.; Mashhadi, S. B.; Okyay, Ali Kemal
One of the effective approaches to reduce residual pores in powder metallurgy parts is activated liquid-phase sintering process using proper additives. In this work, for the first time, a new biocompatible additive (Mn-11.5 wt.% Si, a eutectic alloy) is experimented for liquid-phase sintering of nanocrystalline/amorphous P558 stainless steel powders. It is realized that by increasing the sintering aid content and temperature, the density is effectively increased: a sharp densification progress when the sintering temperature increases from 1000 °C to 1050 °C and a slower densification rate when it exceeds 1050 °C. This preliminary study opens up the development of high-density medical-grade stainless steels produced by powder metallurgy, where suitable additives can lower sintering temperature and time, which is promising for retarding grain growth and commercial applications.
Open Access
Metamaterials as broadband absorbers, tunable color filters, and multi-functional metasurfaces
(2019-06) Aalizadeh, Majid
Metamaterials have enabled us to come up with artificial structures and designs that can perform optical functionalities which are not achievable with natural materials. Here we design and implement three important applications of metamaterials as: 1. Ultra-broadband absorbers, 2. Real-time tunable color filters, and 3. Wideband and wide-angle efficient beam deflector and Multi-functional angular filter. By lithogra-phy being a major hinder on the way to mass production and cost-effectiveness, most of our works are lithography-free. We have introduced Manganese (Mn) for the first time as a very promising metal for broadband absorption and have used it in all our works. Four different Mn-based broadband absorbers are designed and fabricated in different chapters. Mn is used in the Metal-Insulator-Metal (MIM) cavity, annealed MIM configuration, top-layer-patterned MIM configuration, and random nanopyra-mids. It is shown in all works that Mn has a much better performance compared to other metals. For instance, in the work based on random nanopyramids, we obtain ultraviolet (UV) to far-infrared (FIR) perfect absorption by exploiting a lithography-free method and only by coating a single Mn layer on a high-roughness substrate. Moreover, using the combination of the MIM cavity and an electro-optic material, we have shown that a lithography-free color filter can be achieved that covers the whole visible spectrum by changing the voltage from -12 to 12 volts. Finally, in a structure composed of Silicon nano-rods, an ultra-wideband and wide-angle highly-efficient beam deflection is obtained. What makes the same structure very promising is that it also has multifunctional applications as band-pass, band-stop, and low-pass angular filter.
Open Access
Mn2+-doped CdSe/CdS core/multishell colloidal quantum wells enabling tunable carrier-dopant exchange interactions
(American Chemical Society, 2015) Delikanlı, S.; Akgül, M. Z.; Murphy, J. R.; Barman, B.; Tsai, Y.; Scrace, T.; Zhang, P.; Bozok, B.; Hernández-Martínez, P.L.; Christodoulides, J.; Cartwright, A. N.; Petrou, A.; Demir, Hilmi Volkan
In this work, we report the manifestations of carrier-dopant exchange interactions in colloidal Mn2+-doped CdSe/CdS core/multishell quantum wells. The carrier-magnetic ion exchange interaction effects are tunable through wave function engineering. In our quantum well heterostructures, manganese was incorporated by growing a Cd0.985Mn0.015S monolayer shell on undoped CdSe nanoplatelets using the colloidal atomic layer deposition technique. Unlike previously synthesized Mn2+-doped colloidal nanostructures, the location of the Mn ions was controlled with atomic layer precision in our heterostructures. This is realized by controlling the spatial overlap between the carrier wave functions with the manganese ions by adjusting the location, composition, and number of the CdSe, Cd1-xMnxS, and CdS layers. The photoluminescence quantum yield of our magnetic heterostructures was found to be as high as 20% at room temperature with a narrow photoluminescence bandwidth of ∼22 nm. Our colloidal quantum wells, which exhibit magneto-optical properties analogous to those of epitaxially grown quantum wells, offer new opportunities for solution-processed spin-based semiconductor devices. © 2015 American Chemical Society.
Open Access
MnOx-Promoted pdAg alloy nanoparticles for the additive-free dehydrogenation of formic acid at room temperature
(American Chemical Society, 2015) Bulut, A.; Yurderi, M.; Karatas, Y.; Say, Z.; Kivrak H.; Kaya, M.; Gulcan, M.; Ozensoy, E.; Zahmakiran, M.
Formic acid (HCOOH) has a great potential as a safe and a convenient hydrogen carrier for fuel cell applications. However, efficient and CO-free hydrogen production through the decomposition of formic acid at low temperatures (<363 K) in the absence of additives constitutes a major challenge. Herein, we present a new heterogeneous catalyst system composed of bimetallic PdAg alloy and MnOx nanoparticles supported on amine-grafted silica facilitating the liberation of hydrogen at room temperature through the dehydrogenation of formic acid in the absence of any additives with remarkable activity (330 mol H2·mol catalyst-1·h-1) and selectivity (>99%) at complete conversion (>99%). Moreover this new catalytic system enables facile catalyst recovery and very high stability against agglomeration, leaching, and CO poisoning. Through a comprehensive set of structural and functional characterization experiments, mechanistic origins of the unusually high catalytic activity, selectivity, and stability of this unique catalytic system are elucidated. Current heterogeneous catalytic architecture presents itself as an excellent contender for clean hydrogen production via room-temperature additive-free dehydrogenation of formic acid for on-board hydrogen fuel cell applications.
Open Access
On the number of bins in equilibria for signaling games
(IEEE, 2019-07) Sarıtaş, Serkan; Yüksel, Serdar; Gezici, Sinan
We investigate the equilibrium behavior for the decentralized quadratic cheap talk problem in which an encoder and a decoder, viewed as two decision makers, have misaligned objective functions. In prior work, we have shown that the number of bins under any equilibrium has to be at most countable, generalizing a classical result due to Crawford and Sobel who considered sources with density supported on [0, 1]. In this paper, we refine this result in the context of exponential and Gaussian sources. For exponential sources, a relation between the upper bound on the number of bins and the misalignment in the objective functions is derived, the equilibrium costs are compared, and it is shown that there also exist equilibria with infinitely many bins under certain parametric assumptions. For Gaussian sources, it is shown that there exist equilibria with infinitely many bins.
Open Access
Phase transformation during mechano-synthesis of nanocrystalline/amorphous Fe–32Mn–6Si alloys
(Elsevier, 2013) Amini, R.; Shamsipoor, A.; Ghaffari, M.; Alizadeh, M.; Okyay, Ali Kemal
Mechano-synthesis of Fe-32Mn-6Si alloy by mechanical alloying of the elemental powder mixtures was evaluated by running the ball milling process under an inert argon gas atmosphere. In order to characterize the as-milled powders, powder sampling was performed at predetermined intervals from 0.5 to 192 h. X-ray florescence analyzer, X-ray diffraction, scanning electron microscope, and high resolution transmission electron microscope were utilized to investigate the chemical composition, structural evolution, morphological changes, and microstructure of the as-milled powders, respectively. According to the results, the nanocrystalline Fe-Mn-Si alloys were completely synthesized after 48 h of milling. Moreover, the formation of a considerable amount of amorphous phase during the milling process was indicated by quantitative X-ray diffraction analysis as well as high resolution transmission electron microscopy image and its selected area diffraction pattern. It was found that the α-to-γ and subsequently the amorphous-to-crystalline (especially martensite) phase transformation occurred by milling development.
Open Access
Spin-polarized ballistic transport in a thin superlattice of zinc blende half-metallic compounds
(The American Physical Society, 2005) Qian, M. C.; Fong, C. Y.; Pickett, W. E.; Pask, J. E.; Yang, L. H.; Dag, S.
We examine theoretically ballistic conduction in thin layers of zinc blende half metals, considering as an example a superlattice consisting of monolayers of GaAs and MnAs, a bilayer of CrAs, and a bilayer of GaAs. By artificially separating bilayers, we show that surface states thwart half metallicity. However, capping the metal-As bilayers restores half metallicity, and ballistic conduction of electrons within ∼0.3 eV of the Fermi level will give nearly 100% spin-polarized transmission in the direction of the superlattice. Recent developments suggest atomic layer epitaxy can be used to produce such thin layers for spintronic applications.
Open Access
Synthesis of fluorescent core-shell nanomaterials and strategies to generate white light
(American Institute of Physics Inc., 2015) Singh, A.; Kaur, R.; Pandey, O. P.; Wei, X.; Sharma, M.
In this work, cadmium free core-shell ZnS:X/ZnS (X-=-Mn, Cu) nanoparticles have been synthesized and used for white light generation. First, the doping concentration of Manganese (Mn) was varied from 1% to 4% to optimize the dopant related emission and its optimal value was found to be 1%. Then, ZnS shell was grown over ZnS:Mn(1%) core to passivate the surface defects. Similarly, the optimal concentration of Copper (Cu) was found to be 0.8% in the range varied from 0.6% to 1.2%. In order to obtain an emission in the whole visible spectrum, dual doping of Mn and Cu was done in the core and the shell, respectively. A solid-solid mixing in different ratios of separately doped quantum dots (QDs) emitting in the blue green and the orange region was performed. Results show that the optimum mixture of QDs excited at 300-nm gives Commission Internationale del'Éclairage color coordinates of (0.35, 0.36), high color rendering index of 88, and correlated color temperature of 4704-K with minimum self-absorption. © 2015 AIP Publishing LLC.
Open Access
Trimetalic heterogeneous catalyst for dehydrogenation of formic acid with enhanced CO tolerance
(2017-09) Perşembe, Elif
Hydrogen energy is considered to be a promising alternative for the sustainable and environmentally friendly solution of the global energy problem. One of the major obstacles of hydrogen energy applications is to maintain safe and efficient storage of hydrogen which can also be achieved chemically using suitable carrier materials. Formic acid (HCOOH, FA) can be utilized as a hydrogen carrier due to its low molecular weight (46 g/mol) and high hydrogen density (%4.4 weight). FA is a stable, non-flammable, and non-toxic biomass side-product rendering it a perfect candidate for an alternative hydrogen vector. Design of novel heterogeneous catalysts which can substitute the existing homogeneous catalytic systems may allow overcoming catalyst isolation and recovery costs and associated logistical problems hindering their applications in on-board operations. FA can be catalytically decomposed via dehydrogenation and dehydration reactions. Selective dehydrogenation of FA is crucial because, the production of CO from dehydration mechanism can suppress the activity of the catalyst by blocking/poisoning the precious metal sites. Consequently, development of CO-resistant, selective, catalytically active, and reusable heterogeneous catalysts has a great significance. In the current work, a new material that can produce H2(g) from FA under ambient conditions in the absence of additives with high CO-poisoning tolerance will be introduced, which is comprised of Pd-based trimetallic active centers functionalized with Ag and Cr in addition to amine-functionalized MnOx promoters dispersed on a SiO2 support surface. A novel trimetallic FA dehydrogenation catalyst was prepared and studied using analytical, ex-situ and in-situ spectroscopic techniques and compared to the results obtained for monometallic, bimetallic and active site-free counterparts. Trimetallic catalysts were found to reveal superior catalytic activity and stability compared to all of the currently investigated catalysts. Structural and catalytic properties of the trimetallic catalysts were investigated as a function of metal loadings. Structural characterization of the synthesized materials was carried out by Raman spectroscopy, Inductively-Coupled Plasma Optical Emission Spectroscopy (ICP-OES), X-ray Diffraction (XRD), Brunauer, Emmett and Teller (BET) Specific Surface Area Analysis, Transmission Electron Microscopy (TEM), High Resolution TEM (HRTEM), Scanning Transmission Electron Microscopy (STEM), and STEM/Energy Dispersive X-Ray (EDX), High-Angle Annular Dark Field (HAADF)/STEM. In addition, interaction of the catalyst surfaces with reactants and products were also monitored via in-situ FTIR spectroscopy for functional characterization. Detailed in-situ FTIR spectroscopic experiments were also performed using HCOOD, DCOOH and DCOOD in order to understand the nature of the adsorbed species, products and catalytic inhibitors.
Open Access
Unpinning of heavy hole spin in magnetic quantum dots
(Wiley-VCH Verlag, 2017) Dinu, I. V.; Moldoveanu, V.; Dragomir, R.; Tanatar, Bilal
Using the k · p theory and configuration interaction method, we analyze the effect of heavy hole–light hole (HH–LH) mixing in CdTe quantum dots (QDs) with a single manganese (Mn) ion. We find that the hole-Mn exchange switches the coupling between two excitons whose Luttinger spinors have both HH and LH components. If the magnetic dopant is off-centered and the QD is subjected to a single π pulse the system periodically bounces between bright and dark mostly HH excitons with opposite HH spins. A pump-and-probe setup allows to estimate the efficiency of this HH spin unpinning from the biexciton response. The biexciton absorption spectrum is also discussed.
Open Access
XPS characterization of Bi and Mn collected on atom-trapping silica for AAS
(Sage Publications, Inc., 1999) Süzer, Şefik; Ertas, N.; Ataman, O. Y.
The chemical state of analyte species collected on a water-cooled silica tube during atom-trapping atomic absorption spectrometric determination is investigated with the use of X-ray photoelectron spectroscopy (XPS) for Bi and Mn. Analysis of the Bi 4f7/2 peak reveals that the chemical state of Bi is +3 during initial trapping (before the atomization stage), but an additional 0-valence state of Bi is also observed after the atomization stage. With the use of the measured Mn 2p3/2 binding energy together with the observed 3s multiplet splitting, the chemical state of Mn is determined as +2 in all stages. Together with our previous determination of 0 valence for Au, it is now postulated that the stability of certain valence states of the three elements (Au, Bi, and Mn) on the silica matrix can be correlated to their electrochemical reduction potentials.