WorldWideScience

Sample records for prepared bimetallic surfaces

  1. Chemical Preparation of Supported Bimetallic Catalysts. Gold-Based Bimetallic, a Case Study

    OpenAIRE

    Louis, Catherine

    2016-01-01

    International audience; This review focuses on the chemical methods used to prepare supported bimetallic heterogeneous catalysts, i.e., bimetallic nanoparticles deposited on a support. The review is limited to the preparation of gold-based bimetallic catalysts and moreover to bimetallic nanoparticles supported on powder inorganic supports, i.e., on the surface or in the porosity, and not on model supports such as single crystals.

  2. Bimetallic nanoparticles: Preparation, properties, and biomedical applications.

    Science.gov (United States)

    Nasrabadi, Hamid Tayefi; Abbasi, Elham; Davaran, Soodabeh; Kouhi, Mohammad; Akbarzadeh, Abolfazl

    2016-01-01

    Many studies of non-supported bimetallic nanoparticle (BMNP) dispersions, stabilized by ligands or polymers, and copolymers, were started only about 10 years ago. Several preparative procedures have been proposed, and full characterizations on BMNPs have been approved. Studies on BMNPs received huge attention from both scientific and technological communities because most of the NPs' catalytic activity depends on their structural aspects. In this study, we focus on the preparation, properties, and bio-application of BMNPs and introduction of the recent advance in these NPs.

  3. Characterization and Preparation of Bimetallic Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Bing; Joe; Hwang; Ching; Hsiang; Chen; Loka; Subramanyam; Sarma; Din-gao; Liu; Jyh; Fu; Lee

    2007-01-01

    1 Results Bimetallic particles in the nanometer size range are of substantial interest due to their vast applications in catalysis[1].The synthesis of bimetallic nanoparticles with definite size with a well-control over their nanostructure remains a challenging problem.Thus there exists a great demand for both synthesis and atomic level characterization of nanostructure of bimetallic nanoparticles (NPs).With the recent advent of high-intensity tunable sources of X-rays,now available at synchrotron radia...

  4. Preparation of Sm–Ru bimetallic alloy films on Ru(0001) surface by vapour-deposition and annealing

    Indian Academy of Sciences (India)

    G Ranga Rao; H Nozoye

    2001-12-01

    Sm–Ru intermetallic surface alloy films were prepared by vacuum deposition and annealing of rare earth Sm on single crystal Ru(0001) surface. The Ru 3 and Sm 3 core level spectra clearly show the formation of surface alloy layers. XPS measurements on surface alloy film revealed an induced peak in the Ru3 region at lower binding energy by 1 eV compared to the bulk Ru (elemental) suggesting an electronic effect of alloying and Sm–Ru bond formation. The Sm 35/2 photoemission peak of Sm film consists of strong features characteristic of Sm(II) with electron configuration 46 (5\\ 6)2 and Sm(III) with electron configuration 46 (5\\ 6)3. It is observed that the Sm(II) feature decreases in intensity upon alloy formation with surface Ru atoms. Oxidation of these films with carbon monoxide indicates alloy breakdown due to the oxidation of Sm atoms selectively. Alloy oxidation also shows a clear shift of Sm 35/2 feature.

  5. Methanol Oxidation on Model Elemental and Bimetallic Transition Metal Surfaces

    DEFF Research Database (Denmark)

    Tritsaris, G. A.; Rossmeisl, J.

    2012-01-01

    Direct methanol fuel cells are a key enabling technology for clean energy conversion. Using density functional theory calculations, we study the methanol oxidation reaction on model electrodes. We discuss trends in reactivity for a set of monometallic and bimetallic transition metal surfaces, flat...... sites on the surface and to screen for novel bimetallic surfaces of enhanced activity. We suggest platinum copper surfaces as promising anode catalysts for direct methanol fuel cells....

  6. Magnetic properties of bimetallic Au/Co nanoparticles prepared by thermal laser treatment

    Science.gov (United States)

    Sosunov, A. V.; Spivak, L. V.

    2016-07-01

    The irradiation of metallic films by a nanosecond pulsed laser leads to a self-assembly of nanoparticle arrays. This method has been used to prepare bimetallic Au/Co nanoparticles on a SiO2 substrate. The microstructure and morphology of the bimetallic nanoparticles have been investigated using scanning electron microscopy and transmission electron microscopy. It has been shown that the bimetallic nanoparticles have a hemispherical shape with a single-crystal structure and an average size of ~50 nm. The magnetic properties of these nanoparticles have been examined using a vibrating-sample magnetometer in the transverse and longitudinal directions. It has been found that the direction of the magnetization of the bimetallic nanoparticles lies in the plane of the substrate, and the coercive forces in the transverse and longitudinal directions differ by 25%. The use of the vibrating-sample magnetometer method makes it possible to investigate the differences in the magnetic saturations and the coercive forces of an array of bimetallic nanoparticles on a large surface area. The performed investigations have demonstrated that the anisotropic nanomagnetic materials with the desired magnetic orientation can be easily and quickly prepared by means of thermal laser treatment.

  7. Controlled surface segregation leads to efficient coke-resistant nickel/platinum bimetallic catalysts for the dry reforming of methane

    KAUST Repository

    Li, Lidong

    2015-02-03

    Surface composition and structure are of vital importance for heterogeneous catalysts, especially for bimetallic catalysts, which often vary as a function of reaction conditions (known as surface segregation). The preparation of bimetallic catalysts with controlled metal surface composition and structure is very challenging. In this study, we synthesize a series of Ni/Pt bimetallic catalysts with controlled metal surface composition and structure using a method derived from surface organometallic chemistry. The evolution of the surface composition and structure of the obtained bimetallic catalysts under simulated reaction conditions is investigated by various techniques, which include CO-probe IR spectroscopy, high-angle annular dark-field scanning transmission electron microscopy, energy-dispersive X-ray spectroscopy, extended X-ray absorption fine structure analysis, X-ray absorption near-edge structure analysis, XRD, and X-ray photoelectron spectroscopy. It is demonstrated that the structure of the bimetallic catalyst is evolved from Pt monolayer island-modified Ni nanoparticles to core-shell bimetallic nanoparticles composed of a Ni-rich core and a Ni/Pt alloy shell upon thermal treatment. These catalysts are active for the dry reforming of methane, and their catalytic activities, stabilities, and carbon formation vary with their surface composition and structure. The reform of reforming: A series of alumina-supported Ni/Pt bimetallic nanoparticles (NPs) with controlled surface composition and structure are prepared. Remarkable surface segregation for these bimetallic NPs is observed upon thermal treatment. These bimetallic NPs are active catalysts for CO2 reforming of CH4, and their catalytic activities, stabilities, and carbon formation vary with their surface composition and structure.

  8. Nanocrystal and surface alloy properties of bimetallic Gold-Platinum nanoparticles

    Directory of Open Access Journals (Sweden)

    Mott Derrick

    2006-01-01

    Full Text Available AbstractWe report on the correlation between the nanocrystal and surface alloy properties with the bimetallic composition of gold-platinum(AuPt nanoparticles. The fundamental understanding of whether the AuPt nanocrystal core is alloyed or phase-segregated and how the surface binding properties are correlated with the nanoscale bimetallic properties is important not only for the exploitation of catalytic activity of the nanoscale bimetallic catalysts, but also to the general exploration of the surface or interfacial reactivities of bimetallic or multimetallic nanoparticles. The AuPt nanoparticles are shown to exhibit not only single-phase alloy character in the nanocrystal, but also bimetallic alloy property on the surface. The nanocrystal and surface alloy properties are directly correlated with the bimetallic composition. The FTIR probing of CO adsorption on the bimetallic nanoparticles supported on silica reveals that the surface binding sites are dependent on the bimetallic composition. The analysis of this dependence further led to the conclusion that the relative Au-atop and Pt-atop sites for the linear CO adsorption on the nanoparticle surface are not only correlated with the bimetallic composition, but also with the electronic effect as a result of the d-band shift of Pt in the bimetallic nanocrystals, which is the first demonstration of the nanoscale core-surface property correlation for the bimetallic nanoparticles over a wide range of bimetallic composition.

  9. Nanocrystal and surface alloy properties of bimetallic Gold-Platinum nanoparticles

    Science.gov (United States)

    Mott, Derrick; Luo, Jin; Smith, Andrew; Njoki, Peter N; Wang, Lingyan

    2007-01-01

    We report on the correlation between the nanocrystal and surface alloy properties with the bimetallic composition of gold-platinum(AuPt) nanoparticles. The fundamental understanding of whether the AuPt nanocrystal core is alloyed or phase-segregated and how the surface binding properties are correlated with the nanoscale bimetallic properties is important not only for the exploitation of catalytic activity of the nanoscale bimetallic catalysts, but also to the general exploration of the surface or interfacial reactivities of bimetallic or multimetallic nanoparticles. The AuPt nanoparticles are shown to exhibit not only single-phase alloy character in the nanocrystal, but also bimetallic alloy property on the surface. The nanocrystal and surface alloy properties are directly correlated with the bimetallic composition. The FTIR probing of CO adsorption on the bimetallic nanoparticles supported on silica reveals that the surface binding sites are dependent on the bimetallic composition. The analysis of this dependence further led to the conclusion that the relative Au-atop and Pt-atop sites for the linear CO adsorption on the nanoparticle surface are not only correlated with the bimetallic composition, but also with the electronic effect as a result of the d-band shift of Pt in the bimetallic nanocrystals, which is the first demonstration of the nanoscale core-surface property correlation for the bimetallic nanoparticles over a wide range of bimetallic composition.

  10. Controlled Surface Segregation Leads to Efficient Coke-Resistant Nickel/Platinum Bimetallic Catalysts for the Dry Reforming of Methane

    Energy Technology Data Exchange (ETDEWEB)

    Li, Lidong [King Abdullah Univ. of Science and Technology, Thuwal (Saudi Arabia); Zhou, Lu [King Abdullah Univ. of Science and Technology, Thuwal (Saudi Arabia); Ould-Chikh, Samy [King Abdullah Univ. of Science and Technology, Thuwal (Saudi Arabia); Anjum, Dalaver H. [King Abdullah Univ. of Science and Technology, Thuwal (Saudi Arabia); Kanoun, Mohammed B. [King Abdullah Univ. of Science and Technology, Thuwal (Saudi Arabia); Scaranto, Jessica [SABIC Corporate Research and Innovation Center, Thuwal (Saudi Arabia); Hedhili, Mohamed N. [King Abdullah Univ. of Science and Technology, Thuwal (Saudi Arabia); Khalid, Syed [Brookhaven National Lab. (BNL), Upton, NY (United States); Laveille, Paco V. [King Abdullah Univ. of Science and Technology, Thuwal (Saudi Arabia); D' Souza, Lawrence [SABIC Corporate Research and Innovation Center, Thuwal (Saudi Arabia); Clo, Alain [King Abdullah Univ. of Science and Technology, Thuwal (Saudi Arabia); Basset, Jean-Marie [King Abdullah Univ. of Science and Technology, Thuwal (Saudi Arabia)

    2015-02-03

    The surface composition and structure are of vital importance for heterogeneous catalysts, especially for bimetallic catalysts, which often vary as a function of reaction conditions (known as surface segregation). The preparation of bimetallic catalysts with controlled metal surface composition and structure is very challenging. In this study, we synthesize a series of Ni/Pt bimetallic catalysts with controlled metal surface composition and structure using a method derived from surface organometallic chemistry. Moreover, the evolution of the surface composition and structure of the obtained bimetallic catalysts under simulated reaction conditions is investigated by various techniques, which include CO-probe IR spectroscopy, high-angle annular dark-field scanning transmission electron microscopy, energy-dispersive X-ray spectroscopy, extended X-ray absorption fine structure analysis, X-ray absorption near-edge structure analysis, XRD, and X-ray photoelectron spectroscopy. It is demonstrated that the structure of the bimetallic catalyst is evolved from Pt monolayer island-modified Ni nanoparticles to core–shell bimetallic nanoparticles composed of a Ni-rich core and a Ni/Pt alloy shell upon thermal treatment. The catalysts are active for the dry reforming of methane, and their catalytic activities, stabilities, and carbon formation vary with their surface composition and structure.

  11. Nanocrystal and surface alloy properties of bimetallic Gold-Platinum nanoparticles

    OpenAIRE

    Mott Derrick; Luo Jin; Smith Andrew; Njoki Peter; Wang Lingyan; Zhong Chuan-Jian

    2006-01-01

    AbstractWe report on the correlation between the nanocrystal and surface alloy properties with the bimetallic composition of gold-platinum(AuPt) nanoparticles. The fundamental understanding of whether the AuPt nanocrystal core is alloyed or phase-segregated and how the surface binding properties are correlated with the nanoscale bimetallic properties is important not only for the exploitation of catalytic activity of the nanoscale bimetallic catalysts, but also to the general exploration of t...

  12. Characterization of Bimetallic Castings with an Austenitic Working Surface Layer and an Unalloyed Cast Steel Base

    Science.gov (United States)

    Wróbel, Tomasz

    2014-05-01

    The paper presents the technology of bimetallic castings based on the founding method of layer coating directly in the cast process of the so-called method of mold cavity preparation. The prepared castings consist of two fundamental parts, i.e., the base and the working surface layer. The base part of the bimetallic casting is typical foundry material, i.e., unalloyed cast steel, whereas the working layer is a plate of austenitic alloy steel sort X2CrNi 18-9. The quality of the joint between the base part and the working layer was evaluated on the basis of ultrasonic non-destructive testing and structure examinations containing metallographic macro- and microscopic studies with the use of a light microscope (LOM) with microhardness measurements and a scanning electron microscope (SEM) with microanalysis of the chemical composition (energy dispersive spectroscopy—EDS). On the basis of the obtained results it was confirmed that the decisive phenomena needed to create a permanent joint between the two components of the bimetallic casting are carbon and heat transport in the direction from the high-carbon and hot base material which was poured into the mold in the form of liquid metal to the low-carbon and cold material of the working layer which was placed in the mold cavity in the form of a monolithic insert.

  13. Controllable Catalysis with Nanoparticles: Bimetallic Alloy Systems and Surface Adsorbates

    KAUST Repository

    Chen, Tianyou

    2016-05-16

    Transition metal nanoparticles are privileged materials in catalysis due to their high specific surface areas and abundance of active catalytic sites. While many of these catalysts are quite useful, we are only beginning to understand the underlying catalytic mechanisms. Opening the “black box” of nanoparticle catalysis is essential to achieve the ultimate goal of catalysis by design. In this Perspective we highlight recent work addressing the topic of controlled catalysis with bimetallic alloy and “designer” adsorbate-stabilized metal nanoparticles.

  14. PROPERTIES OF POLYMER SUPPORTED Ni-Cu BIMETALLIC CATALYSTS PREPARED BY SOLVATED METAL ATOM IMPREGNATION

    Institute of Scientific and Technical Information of China (English)

    WU Shihua; ZHU Changying; HUANG Wenqiang

    1996-01-01

    D-72 resin supported nickel-copper catalysts prepared by solvated metal atom impregnation (SMAI) were studied by magnetic measurements and X-ray photoelectron spectroscopy (XPS). The Ni particles on the catalysts are very highly dispersed and display superparamagnetic behaviour. Ni-Cu alloy clusters were found to be formed. The surface compositions are different from the bulk concentrations. In contrast with the surface enrichment in copper generally observed on conventional Ni-Cu catalysts, the surfaces of these catalysts are enriched in nickel. The nickel is in both zero and valent states, while copper is mainly in metallic state. Catalytic data show that the formation of Ni-Cu alloy clusters has a profound effect on the catalytic activities of the catalysts in the hydrogenation of furfural. The activity of the Ni:Cu ratio of one bimetallic catalysts is much higher than that of the Ni or Cu monometallic catalyst.

  15. Preparation and characterization of planar Ni–Au bimetallic model catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Fan, E-mail: fan.yang@chem.tamu.edu; Yao, Yunxi; Yan, Zhen; Min, Hlaing; Goodman, D. Wayne

    2013-10-15

    Ni–Au bimetallic model catalysts were prepared as thin films on Re(0 0 0 1) or Ru(0 0 0 1) single crystal substrates. Surface compositions and electronic structures of the Ni–Au thin films were characterized by low energy ion scattering spectroscopy and X-ray photoelectron spectroscopy, respectively. Surface alloys were prepared by annealing Ni–Au thin films from 500 to 800 K, resulting in substantial surface enrichment of Au. Annealing a Ni–Au thin film with a 1:1 bulk composition ratio at 700 K for 10 min resulted in a surface alloy with 84% (atomic concentration) of Au in the outermost surface layer. The surface atomic structure was investigated using CO as probe molecules, which exclusively adsorbs on the Ni atoms rather than on the Au atoms at room temperature. Polarization modulation infrared reflection absorption spectroscopy of CO adsorption on Ni–Au surface alloys showed that CO adsorption on two-fold bridge sites decreased and finally disappeared with an increase of Au surface concentration. The absence of Ni bridge site CO adsorption indicated that Ni atoms were isolated by Au atoms on Ni–Au alloyed surface.

  16. Nanostructural Formation of Pd-Co Bimetallic Complex on HOPG Surfaces: XPS and AFM Studies

    Directory of Open Access Journals (Sweden)

    Lisandra Arroyo-Ramírez

    2009-01-01

    Full Text Available A new single source approach was developed to synthesize Pd-Co nanoparticles using a bimetallic compound, [Et3NH]2[CoPd2(μ-4-I-3,5-Me2pz4Cl4] (CoPd2, as a molecular precursor to obtain dispersed catalyst on highly ordered pyrolytic graphite (HOPG surface, in view of preparing oxygen reduction catalysts for low temperature fuel cells. X-ray photoelectron spectroscopy (XPS and atomic force microscopy (AFM techniques were employed to characterize the nanostructure formations and to determine the composition and morphology of the complex on the HOPG. Results of high resolution XPS analysis (HR-XPS revealed the binding energies corresponding to the atomic constituents of the precursor. When the precursor solution was placed on the surface of the HOPG, the bimetallic complex assumes a tubular structure and it appears that the surface of the HOPG offers a ground for the self-organization of nanostructural formations.

  17. Preparation and characterization of Ni/Co bimetallic nano-clusters

    Institute of Scientific and Technical Information of China (English)

    Jinzhang Gao; Fei Guan; Yongjun Ma; Jingwan Kang

    2003-01-01

    Ni/Co bimetallic nano-cluters have been prepared from the aqueous solution by reducing their corresponding metal salts under suitable conditions. The experimental conditions including the type and concentration of protective agent, feeding order and the pH of the solution that influence the average particle size have been studied in detail. Transmission electron microscopy (TEM)indicates that the shape of those bimetallic nano-cluster particles is spheroid. The alloy structure has been shown by X-ray powder diffraction (XRD). The X-ray photoelectron spectroscopic (XPS) data have confirmed that the nickel and cobalt in the bimetallic nano-clusters are in the zero-valence state.

  18. Bimetallic structure fabricated by laser interference lithography for tuning surface plasmon resonance.

    Science.gov (United States)

    Liu, C H; Hong, M H; Cheung, H W; Zhang, F; Huang, Z Q; Tan, L S; Hor, T S A

    2008-07-07

    Tuning of surface plasmon resonance by gold and silver bimetallic thin film and bimetallic dot array is investigated. Laser interference lithography is applied to fabricate the nanostructures. A bimetallic dot structure is obtained by a lift-off procedure after gold and silver thin film deposition by an electron beam evaporator. Surface plasmon behaviors of these films and nanostructures are studied using UV-Vis spectroscopy. It is observed that for gold thin film on quartz substrate, the optical spectral peak is blue shifted when a silver thin film is coated over it. Compared to the plasmon band in single metal gold dot array, the bimetallic nanodot array shows a similar blue shift in its spectral peak. These shifts are both attributed to the interaction between gold and silver atoms. Electromagnetic interaction between gold and silver nanostructures is discussed using a simplified spring model.

  19. Peptide-Directed PdAu Nanoscale Surface Segregation: Toward Controlled Bimetallic Architecture for Catalytic Materials.

    Science.gov (United States)

    Bedford, Nicholas M; Showalter, Allison R; Woehl, Taylor J; Hughes, Zak E; Lee, Sungsik; Reinhart, Benjamin; Ertem, S Piril; Coughlin, E Bryan; Ren, Yang; Walsh, Tiffany R; Bunker, Bruce A

    2016-09-27

    Bimetallic nanoparticles are of immense scientific and technological interest given the synergistic properties observed when two different metallic species are mixed at the nanoscale. This is particularly prevalent in catalysis, where bimetallic nanoparticles often exhibit improved catalytic activity and durability over their monometallic counterparts. Yet despite intense research efforts, little is understood regarding how to optimize bimetallic surface composition and structure synthetically using rational design principles. Recently, it has been demonstrated that peptide-enabled routes for nanoparticle synthesis result in materials with sequence-dependent catalytic properties, providing an opportunity for rational design through sequence manipulation. In this study, bimetallic PdAu nanoparticles are synthesized with a small set of peptides containing known Pd and Au binding motifs. The resulting nanoparticles were extensively characterized using high-resolution scanning transmission electron microscopy, X-ray absorption spectroscopy, and high-energy X-ray diffraction coupled to atomic pair distribution function analysis. Structural information obtained from synchrotron radiation methods was then used to generate model nanoparticle configurations using reverse Monte Carlo simulations, which illustrate sequence dependence in both surface structure and surface composition. Replica exchange with solute tempering molecular dynamics simulations were also used to predict the modes of peptide binding on monometallic surfaces, indicating that different sequences bind to the metal interfaces via different mechanisms. As a testbed reaction, electrocatalytic methanol oxidation experiments were performed, wherein differences in catalytic activity are clearly observed in materials with identical bimetallic composition. Taken together, this study indicates that peptides could be used to arrive at bimetallic surfaces with enhanced catalytic properties, which could be leveraged

  20. Surface Segregation in Bimetallic Nanoparticles: A Critical Issue in Electrocatalyst Engineering.

    Science.gov (United States)

    Liao, Hanbin; Fisher, Adrian; Xu, Zhichuan J

    2015-07-15

    Bimetallic nanoparticles are a class of important electrocatalyst. They exhibit a synergistic effect that critically depends on the surface composition, which determines the surface properties and the adsorption/desorption behavior of the reactants and intermediates during catalysis. The surface composition can be varied, as nanoparticles are exposed to certain environments through surface segregation. Thermodynamically, this is caused by a difference in surface energy between the two metals. It may lead to the enrichment of one metal on the surface and the other in the core. The external conditions that influence the surface energy may lead to the variation of the thermodynamic steady state of the particle surface and, thus, offer a chance to vary the surface composition. In this review, the most recent and important progress in surface segregation of bimetallic nanoparticles and its impact in electrocatalysis are introduced. Typical segregation inducements and surface characterization techniques are discussed in detail. It is concluded that surface segregation is a critical issue when designing bimetallic catalysts. It is necessary to explore methods to control it and utilize it as a way towards producing robust, bimetallic electrocatalysts. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. INTERACTION OF SULPHUR WITH BIMETALLIC SURFACES: EFFECTS OF STRUCTURAL, ELECTRONIC AND CHEMICAL PROPERTIES.

    Energy Technology Data Exchange (ETDEWEB)

    RODRIGUEZ,J.A.; HRBEK,J.

    2001-10-04

    In recent years, several new interesting phenomena have been discovered when studying the interaction of sulphur with bimetallic surfaces using the modern techniques of surface science. Very small amounts of sulphur can induce dramatic changes in the morphology of bimetallic surfaces. The electronic perturbations associated with the formation of a heteronuclear metal-metal bond affect the reactivity of the bonded metals toward sulphur. This can be a very important issue to consider when trying to minimize the negative effects of sulphur poisoning or dealing with the design of desulfurization catalysts.

  2. Bimetallic nanostructures as active Raman markers: gold-nanoparticle assembly on 1D and 2D silver nanostructure surfaces.

    Science.gov (United States)

    Gunawidjaja, Ray; Kharlampieva, Eugenia; Choi, Ikjun; Tsukruk, Vladimir V

    2009-11-01

    It is demonstrated that bimetallic silver-gold anisotropic nanostructures can be easily assembled from various nanoparticle building blocks with well-defined geometries by means of electrostatic interactions. One-dimensional (1D) silver nanowires, two-dimensional (2D) silver nanoplates, and spherical gold nanoparticles are used as representative building blocks for bottom-up assembly. The gold nanoparticles are electrostatically bound onto the 1D silver nanowires and the 2D silver nanoplates to give bimetallic nanostructures. The unique feature of the resulting nanostructures is the particle-to-particle interaction that subjects absorbed analytes to an enhanced electromagnetic field with strong polarization dependence. The Raman activity of the bimetallic nanostructures is compared with that of the individual nanoparticle blocks by using rhodamine 6G solution as the model analyte. The Raman intensity of the best-performing silver-gold nanostructure is comparable with the dense array of silver nanowires and silver nanoplates that were prepared by means of the Langmuir-Blodgett technique. An optimized design of a single-nanostructure substrate for surface-enhanced Raman spectroscopy (SERS), based on a wet-assembly technique proposed here, can serve as a compact and low-cost alternative to fabricated nanoparticle arrays.

  3. Influence of complexing agents on the preparation of bimetallic platinum-ruthenium catalysts supported on O-functionalized graphite cloths

    Energy Technology Data Exchange (ETDEWEB)

    Sieben, J.M., E-mail: jmsieben@uns.edu.a [Instituto de Ingenieria Electroquimica y Corrosion (INIEC), Universidad Nacional del Sur., Av. Alem 1253, (B8000CPB) Bahia Blanca (Argentina); Duarte, M.M.E.; Mayer, C.E. [Instituto de Ingenieria Electroquimica y Corrosion (INIEC), Universidad Nacional del Sur., Av. Alem 1253, (B8000CPB) Bahia Blanca (Argentina)

    2010-02-18

    Electrodeposition of bimetallic Pt-Ru catalysts on O-functionalized graphite cloths from H{sub 2}PtCl{sub 6} and RuCl{sub 3} solutions containing trisodium citrate (Cit) and disodium dihydrogen ethylenediaminetetraacetate (Na{sub 2}H{sub 2}EDTA) was investigated. SEM analysis of the electrode prepared without complexant showed a relatively compact and rough deposit displaying a 'tree cortex' structure, whereas uniform size and globular shape particles regularly distributed over the support surface were obtained using citrate and Na{sub 2}H{sub 2}EDTA as complexants. In addition, XRD diffraction and EDX analysis revealed that the catalysts prepared using the complexants showed smaller size particles and lower Ru content. Electrocatalytic activity measurements indicated that the most active electrode for methanol oxidation was obtained with Na{sub 2}H{sub 2}EDTA as additive.

  4. Theoretical studies of the work functions of Pd-based bimetallic surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Zhao-Bin; Wu, Feng; Wang, Yue-Chao; Jiang, Hong, E-mail: jianghchem@pku.edu.cn [Beijing National Laboratory of Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871 (China)

    2015-06-07

    Work functions of Pd-based bimetallic surfaces, including mainly M/Pd(111), Pd/M, and Pd/M/Pd(111) (M = 4d transition metals, Cu, Au, and Pt), are studied using density functional theory. We find that the work function of these bimetallic surfaces is significantly different from that of parent metals. Careful analysis based on Bader charges and electron density difference indicates that the variation of the work function in bimetallic surfaces can be mainly attributed to two factors: (1) charge transfer between the two different metals as a result of their different intrinsic electronegativity, and (2) the charge redistribution induced by chemical bonding between the top two layers. The first factor can be related to the contact potential, i.e., the work function difference between two metals in direct contact, and the second factor can be well characterized by the change in the charge spilling out into vacuum. We also find that the variation in the work functions of Pd/M/Pd(111) surfaces correlates very well with the variation of the d-band center of the surface Pd atom. The findings in this work can be used to provide general guidelines to design new bimetallic surfaces with desired electronic properties.

  5. Surface composition tuning of Au-Pt bimetallic nanoparticles for enhanced carbon monoxide and methanol electro-oxidation.

    Science.gov (United States)

    Suntivich, Jin; Xu, Zhichuan; Carlton, Christopher E; Kim, Junhyung; Han, Binghong; Lee, Seung Woo; Bonnet, Nicéphore; Marzari, Nicola; Allard, Lawrence F; Gasteiger, Hubert A; Hamad-Schifferli, Kimberly; Shao-Horn, Yang

    2013-05-29

    The ability to direct bimetallic nanoparticles to express desirable surface composition is a crucial step toward effective heterogeneous catalysis, sensing, and bionanotechnology applications. Here we report surface composition tuning of bimetallic Au-Pt electrocatalysts for carbon monoxide and methanol oxidation reactions. We establish a direct correlation between the surface composition of Au-Pt nanoparticles and their catalytic activities. We find that the intrinsic activities of Au-Pt nanoparticles with the same bulk composition of Au0.5Pt0.5 can be enhanced by orders of magnitude by simply controlling the surface composition. We attribute this enhancement to the weakened CO binding on Pt in discrete Pt or Pt-rich clusters surrounded by surface Au atoms. Our finding demonstrates the importance of surface composition control at the nanoscale in harnessing the true electrocatalytic potential of bimetallic nanoparticles and opens up strategies for the development of highly active bimetallic nanoparticles for electrochemical energy conversion.

  6. A facile reflux procedure to increase active surface sites form highly active and durable supported palladium@platinum bimetallic nanodendrites

    Science.gov (United States)

    Wang, Qin; Li, Yingjun; Liu, Baocang; Xu, Guangran; Zhang, Geng; Zhao, Qi; Zhang, Jun

    2015-11-01

    A series of well-dispersed bimetallic Pd@Pt nanodendrites uniformly supported on XC-72 carbon black are fabricated by using different capping agents. These capping agents are essential for the branched morphology control. However, the surfactant adsorbed on the nanodendrites surface blocks the access of reactant molecules to the active surface sites, and the catalytic activities of these bimetallic nanodendrites are significantly restricted. Herein, a facile reflux procedure to effectively remove the capping agent molecules without significantly affecting their sizes is reported for activating supported nanocatalysts. More significantly, the structure and morphology of the nanodendrites can also be retained, enhancing the numbers of active surface sites, catalytic activity and stability toward methanol and ethanol electro-oxidation reactions. The as-obtained hot water reflux-treated Pd@Pt/C catalyst manifests superior catalytic activity and stability both in terms of surface and mass specific activities, as compared to the untreated catalysts and the commercial Pt/C and Pd/C catalysts. We anticipate that this effective and facile removal method has more general applicability to highly active nanocatalysts prepared with various surfactants, and should lead to improvements in environmental protection and energy production.

  7. The adsorption and decomposition of methane on Fe/Cu(110)bimetallic surface

    Institute of Scientific and Technical Information of China (English)

    鲍世宁; 范朝阳; 李海洋; 徐亚伯

    1995-01-01

    The adsorption and decomposition of methane on Fe/Cu(110) bimetallic surface have been studied by HREELS and ARUPS. The results show that the activation energy of dissociative chemisorption for methane is reduced obviously by preadsorption of iron on copper surface. The chemisorption probability of methane is so high on Fe/Cu(110) bimetallic surface that chemisorption of methane can be observed at room temperature and low pressure. When the iron coverage is lower than 1 ML, the chemisorption probability increases linearly with increasing iron coverage. After the iron coverage is beyond 1 ML(<2ML) the probability continues increasing. The iron atom with disordered structure can offer the site of dissociative chemisorption to methane too. A hydroformyl species is formed through interaction between methane and the preadsorbed oxygen atoms. The reaction enhances the dissociative chemisorption of methane on the surface.

  8. Using supported Au nanoparticles as starting material for preparing uniform Au/Pd bimetallic catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Villa, Alberto [Universita di Milano, Italy; Prati, Laura [Universita di Milano, Italy; Su, Dangshen [Fritz Haber Institute of the Max Planck Society, Berlin, Germany; Wang, Di [Fritz Haber Institute of the Max Planck Society, Berlin, Germany; Veith, Gabriel M [ORNL

    2010-01-01

    One of the best methods for producing bulk homogeneous (composition) supported bimetallic AuPd clusters involves the immobilization of a protected Au seed followed by the addition of Pd. This paper investigates the importance of this gold seed in controlling the resulting bimetallic AuPd clusters structures, sizes and catalytic activities by investigating three different gold seeds. Uniform Au-Pd alloy were obtained when a steric/electrostatic protecting group, poly(vinyl alcohol) (PVA), was used to form the gold clusters on activated carbon (AC). In contrast Au/AC precursors prepared using Au nanoparticles with only electrostatic stabilization (tetrakis(hydroxypropyl)phosphonium chloride (THPC)), or no stabilization (magnetron sputtering) produced inhomogeneous alloys and segregation of the gold and palladium. The uniform alloyed catalyst (Pd{at}Au{sub PVA}/AC) is the most active and selective catalyst, while the inhomogenous catalysts are less active and selective. Further study of the PVA protected Au clusters revealed that the amount of PVA used is also critical for the preparation of uniform alloyed catalyst, their stability, and their catalytic activity.

  9. On Metal Segregation of Bimetallic Nanocatalysts Prepared by a One-Pot Method in Microemulsions

    Directory of Open Access Journals (Sweden)

    Concha Tojo

    2017-02-01

    Full Text Available A comparative study on different bimetallic nanocatalysts prepared from microemulsions using a one-pot method has been carried out. The analysis of experimental observations, complemented by simulation studies, provides detailed insight into the factors affecting nanoparticle architecture: (1 The metal segregation in a bimetallic nanocatalysts is the result of the combination of three main kinetic parameters: the reduction rate of metal precursors (related to reduction standard potentials, the material intermicellar exchange rate (determined by microemulsion composition, and the metal precursors concentration; (2 A minimum difference between the reduction standard potentials of the two metals of 0.20 V is needed to obtain a core-shell structure. For values ∆ε0 smaller than 0.20 V the obtaining of alloys cannot be avoided, neither by changing the microemulsion nor by increasing metal concentration; (3 As a rule, the higher the film flexibility around the micelles, the higher the degree of mixture in the nanocatalyst; (4 A minimum concentration of metal precursors is required to get a core-shell structure. This minimum concentration depends on the microemulsion flexibility and on the difference in reduction rates.

  10. Ag-Cu Bimetallic Nanoparticles Prepared by Microemulsion Method as Catalyst for Epoxidation of Styrene

    Directory of Open Access Journals (Sweden)

    Hong-Kui Wang

    2012-01-01

    Full Text Available Ag/Cu bimetallic nanocatalysts supported on reticulate-like γ-alumina were prepared by a microemulsion method using N2H4·H2O as the reducing agent. The catalysts were activated by calcination followed with hydrogen reduction at 873K, and the properties were confirmed using various characterization techniques. Compared with metal oxides particles, Ag-Cu particles exhibited smaller sizes (<5 nm after calcination in H2 at 873K. XPS results indicated that the binding energies changed with the Ag/Cu ratios, suggesting that increasing the copper content gave both metals a greater tendency to lose electrons. Furthermore, Ag-Cu bimetallic nanoparticles supported on γ-alumina showed better catalytic activity on the epoxidation of styrene as compared with the corresponding monometallic silver or copper. The styrene oxide selectivity could reach 76.6% at Ag/Cu molar ratio of 3/1, while the maximum conversion (up to 94.6% appeared at Ag/Cu molar ratio of 1/1 because of the maximum interaction between silver and copper.

  11. Reaction pathways of furfural, furfuryl alcohol and 2-methylfuran on Cu(111) and NiCu bimetallic surfaces

    Science.gov (United States)

    Xiong, Ke; Wan, Weiming; Chen, Jingguang G.

    2016-10-01

    Hydrodeoxygenation (HDO) is an important reaction for converting biomass-derived furfural to value-added 2-methylfuran, which is a promising fuel additive. In this work, the HDO of furfural to produce 2-methylfuran occurred on the NiCu bimetallic surfaces prepared on either Ni(111) or Cu(111). The reaction pathways of furfural were investigated on Cu(111) and Ni/Cu(111) surfaces using density functional theory (DFT) calculations, temperature-programmed desorption (TPD) and high-resolution electron energy loss spectroscopy (HREELS) experiments. These studies provided mechanistic insights into the effects of bimetallic formation on enhancing the HDO activity. Specifically, furfural weakly adsorbed on Cu(111), while it strongly adsorbed on Ni/Cu(111) through an η2(C,O) configuration, which led to the HDO of furfural on Ni/Cu(111). The ability to dissociate H2 on Ni/Cu(111) is also an important factor for enhancing the HDO activity over Cu(111).

  12. Core–Shell Bimetallic Nanoparticles Robustly Fixed on the Outermost Surface of Magnetic Silica Microspheres

    Science.gov (United States)

    Park, Hye Hun; Woo, Kyoungja; Ahn, Jae-Pyoung

    2013-01-01

    The major challenges in practically utilising the immense potential benefits of nanomaterials are controlling aggregation, recycling the nanomaterials, and fabricating well-defined nanoparticulate materials using innovative methods. We present a novel innovative synthetic strategy for core–shell bimetallic nanoparticles that are well-defined, ligand-free, and robustly fixed on the outermost surface of recyclable magnetic silica microspheres. The strategy includes seeding, coalescing the seeds to cores, and then growing shells from the cores on aminopropyl-functionalised silica microspheres so that the cores and aminopropyl moieties are robustly embedded in the shell materials. The representative Au–Ag bimetallic nanoparticles fixed on the microsphere showed excellent catalytic performance that remained consistent during repeated catalytic cycles. PMID:23511209

  13. On the performance of surface plasmon resonance based fibre optic sensor with different bimetallic nanoparticle alloy combinations

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Anuj K; Mohr, Gerhard J [Institute of Physical Chemistry, Friedrich-Schiller University, Lessingstrasse 10, 07743 Jena (Germany)], E-mail: anuj.sharma@uni-jena.de

    2008-03-07

    In this work, we have investigated the capability of different bimetallic nanoparticle alloy combinations to be used in fibre optic sensors based on the technique of surface plasmon resonance. The metals considered for this analysis are silver, gold, copper and aluminium. The performance of the sensor with different bimetallic nanoparticle alloy combinations is evaluated and compared numerically. The performance is analysed in terms of three parameters: sensitivity, signal-to-noise ratio (SNR) and operating range for the sensing layer refractive index values. On the basis of the comparison and some logistic criteria, the best possible bimetallic alloy combinations along with a requisite alloy composition ratio are predicted. The bimetallic nanoparticle alloy combination is capable of simultaneously providing larger values of sensitivity, SNR and operating range, which is not possible with any single metallic nanoparticle layer.

  14. Sn surface-enriched Pt-Sn bimetallic nanoparticles as a selective and stable catalyst for propane dehydrogenation

    KAUST Repository

    Zhu, Haibo

    2014-12-01

    A new one pot, surfactant-free, synthetic route based on the surface organometallic chemistry (SOMC) concept has been developed for the synthesis of Sn surface-enriched Pt-Sn nanoparticles. Bu3SnH selectively reacts with [Pt]-H formed in situ at the surface of Pt nanoparticles, Pt NPs, obtained by reduction of K2PtCl4 by LiB(C2H5)3H. Chemical analysis, 1H MAS and 13C CP/MAS solid-state NMR as well as two-dimensional double-quantum (DQ) and triple-quantum (TQ) experiments show that organo-tin moieties Sn(n-C4H9) are chemically linked to the surface of Pt NPs to produce, in fine, after removal of most of the n-butyl fragment, bimetallic Pt-Sn nanoparticles. The Sn(n-CH2CH2CH2CH3) groups remaining at the surface are believed to stabilize the as-synthesized Pt-Sn NPs, enabling the bimetallic NPs to be well dispersed in THF. Additionally, the Pt-Sn nanoparticles can be supported on MgAl2O4 during the synthesis of the nanoparticles. Some of the Pt-Sn/MgAl2O4 catalyst thus prepared exhibits high activity in PROX of CO and an extremely high selectivity and stability in propane dehydrogenation to propylene. The enhanced activity in propane dehydrogenation is associated with the high concentration of inactive Sn at the surface of Pt nanoparticles which ”isolates” the active Pt atoms. This conclusion is confirmed by XRD, NMR, TEM, and XPS analysis.

  15. Surface plasmon resonance sensing of a biomarker of Alzheimer disease in an intensity measurement mode with a bimetallic chip

    Science.gov (United States)

    Kim, Hyung Jin; Sohn, Young-Soo; Kim, Chang-duk; Jang, Dae-ho

    2016-09-01

    A surface plasmon resonance (SPR) sensor system with a bimetallic chip has been utilized to sense the very low concentration of amyloid-beta (A β)(1-42) by measurement of the reflectance variation. The bimetallic chip was comprised of Au (10 nm) and Ag (40 nm) on Cr (2 nm)-coated BK-7 glass substrate. Protein A was used to efficiently immobilize the antibody of A β(1-42) on the surface of the bimetallic chip. The reflectance curve of the bimetallic chip represented a narrower linewidth compared to that of the conventional gold (Au) chip. The SPR sensor using the bimetallic chip in the intensity interrogation mode acquired the response of A β(1-42) at concentrations of 250, 500, 750 and 1,000 pg/ml. The calibration plot showed a linear relationship between the mean reflectance variation and the A β(1-42) concentration. The results proved that the SPR sensor system with the bimetallic chip in the intensity interrogation mode can successfully detect various concentrations of A β(1-42), including critical concentration, to help diagnose Alzheimer's disease.

  16. PREPARATION OF NOVEL METALLIC AND BIMETALLIC CROSS-LINKED POLY (VINYL ALCOHOL) NANOCOMPOSITES UNDER MICROWAVE IRRADIATION

    Science.gov (United States)

    A facile method utilizing microwave irradiation is described that accomplishes the cross-linking reaction of PVA with metallic and bimetallic systems. Nanocomposites of PVA-cross-linked metallic systems such as Pt, Cu, and In and bimetallic systems such as Pt-In, Ag-Pt, Pt-Fe, Cu...

  17. NOVEL METALLIC AND BIMETALLIC CROSS-LINKED POLY (VINYL ALCOHOL) NANOCOMPOSITES PREPARED UNDER MICROWAVE IRRADIATION

    Science.gov (United States)

    A facile microwave irradiation approach that results in a cross-linking reaction of poly (vinyl alcohol) (PVA) with metallic and bimetallic systems is described. Nanocomposites of PVA cross-linked metallic systems such as Pt, Cu, and In and bimetallic systems such as Pt-In, Ag-P...

  18. Preparation of bimetallic nanoparticles using a facile green synthesis method and their application.

    Science.gov (United States)

    Xia, Bihua; He, Fang; Li, Lidong

    2013-04-16

    A straightforward, economically viable, and green approach for the synthesis of well-stabilized Au/Ag bimetallic nanoparticles is described; this method uses nontoxic and renewable degraded pueraria starch (DPS) as a matrix and mild reaction conditions. The DPS acted as both a reducing agent and a capping agent for the bimetallic nanoparticles. Au/Ag bimetallic nanoparticles were successfully grown within the DPS matrixes, and the bimetallic structures were characterized using various methods, including high-resolution transmission electron microscopy, energy-dispersive X-ray, and X-ray diffraction. Moreover, it was shown that these DPS-capped Au/Ag bimetallic nanoparticles could function as catalysts for the reduction of 4-nitrophenol in the presence of NaBH4 and were more effective than Au or Ag monometallic nanoparticles.

  19. Characterization of Bimetallic Fe-Ru Oxide Nanoparticles Prepared by Liquid-Phase Plasma Method

    Science.gov (United States)

    Lee, Sung-Jin; Lee, Heon; Jeon, Ki-Joon; Park, Hyunwoong; Park, Young-Kwon; Jung, Sang-Chul

    2016-07-01

    The bimetallic Fe-Ru oxide nanoparticles were synthesized in the liquid-phase plasma (LPP) method which employed iron chloride and ruthenium chloride as precursors. The active species (OH·, Hα, Hβ, and OI) and the iron and ruthenium ions were observed in the plasma field created by the LPP process. The spherical-shaped bimetallic Fe-Ru oxide nanoparticles were synthesized by the LPP reaction, and the size of the particles was growing along with the progression of the LPP reaction. The synthesized bimetallic Fe-Ru oxide nanoparticles were comprised of Fe2O3, Fe3O4, RuO, and RuO2. Ruthenium had a higher reduction potential than iron and resulted in higher ruthenium composition in the synthesized bimetallic nanoparticles. The control of the molar ratio of the precursors in the reactant solution was found to be employed as a means to control the composition of the elements in bimetallic nanoparticles.

  20. Understanding the atomic-level process of CO-adsorption-driven surface segregation of Pd in (AuPd)147 bimetallic nanoparticles.

    Science.gov (United States)

    An, Hyesung; Ha, Hyunwoo; Yoo, Mi; Kim, Hyun You

    2017-08-24

    When the elements that compose bimetallic catalysts interact asymmetrically with reaction feedstock, the surface concentration of the bimetallic catalysts and the morphology of the reaction center evolve dynamically as a function of environmental factors such as the partial pressure of the triggering molecule. Relevant experimental and theoretical findings of the dynamic structural evolution of bimetallic catalysts under the reaction conditions are emerging, thus enabling the design of more consistent, reliable, and efficient bimetallic catalysts. In an initial attempt to provide an atomic-level understanding of the adsorption-induced structural evolution of bimetallic nanoparticles (NPs) under CO oxidation conditions, we used density functional theory to study the details of CO-adsorption-driven Pd surface segregation in (AuPd)147 bimetallic NPs. The strong CO affinity of Pd provides a driving force for Pd surface segregation. We found that the vertex site of the NP becomes a gateway for the initial Pd-Au swapping and the subsequent formation of an internal vacancy. This self-generated internal vacancy easily diffuses inside the NP and activates Pd-Au swapping pathways in the (100) NP facet. Our results reveal how the surface and internal concentrations of bimetallic NPs respond immediately to changes in the reaction conditions. Our findings should aid in the rational design of highly active and versatile bimetallic catalysts by considering the environmental factors that systematically affect the structure of bimetallic catalysts under the reaction conditions.

  1. Surface plasmon polariton assisted optical switching in noble bimetallic nanoparticle system

    Energy Technology Data Exchange (ETDEWEB)

    Dhara, Sandip, E-mail: dhara@igcar.gov.in, E-mail: chenkh@pub.iams.sinica.edu.tw [Surface and Nanoscience Division, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102 (India); Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 106, Taiwan (China); Lu, C.-Y.; Tu, W.-S. [Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 106, Taiwan (China); Magudapathy, P. [Materials Physics Division, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102 (India); Huang, Y.-F.; Chen, K.-H., E-mail: dhara@igcar.gov.in, E-mail: chenkh@pub.iams.sinica.edu.tw [Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 106, Taiwan (China); Center for Condensed Matter Science, National Taiwan University, Taipei 106, Taiwan (China)

    2015-01-12

    Photoresponse of bimetallic Au-Ag nanoparticle embedded soda glass (Au-Ag@SG) substrate is reported for surface plasmon assisted optical switching using 808 nm excitation. Au-Ag@SG system is made by an ion beam technique where Ag{sup +} is introduced first in the soda glass matrix by ion exchange technique. Subsequently, 400 keV Au{sup +} is implanted in the sample for different fluences, which is followed by an ion beam annealing process using 1 MeV Si{sup +} at a fixed fluence of 2 × 10{sup 16} ions·cm{sup −2}. Characteristic surface plasmon resonance (SPR) peaks around 400 and 550 nm provided evidence for the presence of Au and Ag nanoparticles. An optical switching in the Au-Ag@SG system with 808 nm, which is away from the characteristic SPR peaks of Ag and Au nanoparticles, suggests the possible role of two photon absorption (TPA) owing to the presence of interacting electric dipole in these systems. The role of surface plasmon polariton is emphasized for the propagation of electronic carrier belonging to the conduction electron of Au-Ag system in understanding the observed photoresponse. Unique excitation dependent photoresponse measurements confirm the possible role of TPA process. A competitive interband and intraband transitions in the bimetallic system of Au and Ag, which may be primarily responsible for the observation, are validated qualitatively using finite difference time domain calculations where inter-particle separation of Au and Ag plays an important role. Thus, a smart way of optical switching can be envisaged in noble bimetallic nanocluster system where long wavelength with higher skin depth can be used for communication purpose.

  2. XPS study of silver, nickel and bimetallic silver-nickel nanoparticles prepared by seed-mediated growth

    Energy Technology Data Exchange (ETDEWEB)

    Prieto, Pilar, E-mail: pilar.prieto@uam.es [Departamento de Fisica Aplicada and Instituto de Ciencia de Materiales ' Nicolas Cabrera' , Universidad Autonoma de Madrid, Cantoblanco, 28049 Madrid (Spain); Nistor, Valentin [Departamento de Fisica Aplicada and Instituto de Ciencia de Materiales ' Nicolas Cabrera' , Universidad Autonoma de Madrid, Cantoblanco, 28049 Madrid (Spain); Nouneh, Khalid [Institute for Nanomaterials and Nanotechnology (INANOTECH), Moroccan Foundation for Advanced Science, Innovation and Research (MAScIR), ENSET, Av. Armee Royale, 10100, Rabat (Morocco); Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8520 (Japan); Oyama, Munetaka [Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8520 (Japan); Abd-Lefdil, Mohammed [Laboratory of Materials Physics, University Mohammed V-Agdal, Rabat (Morocco); Diaz, Raquel [Departamento de Fisica Aplicada and Instituto de Ciencia de Materiales ' Nicolas Cabrera' , Universidad Autonoma de Madrid, Cantoblanco, 28049 Madrid (Spain)

    2012-09-01

    Highlights: Black-Right-Pointing-Pointer We have prepared Ag, Ni and AgNi NPs by derived seed-mediated growth method. Black-Right-Pointing-Pointer The combined use of optical, structural and chemical characterization techniques allows to determine the presence of core-shell structures. Black-Right-Pointing-Pointer The oxidation states of Ag and Ni at the outer layers of the NPs have been studied by XPS. Black-Right-Pointing-Pointer Ag NPs are purely metallic with a fcc structure. Black-Right-Pointing-Pointer Ni NPs are formed by Ni core-NiO + Ni(OH){sub 2} shell structure. Black-Right-Pointing-Pointer Ag core-NiO + Ni(OH){sub 2} shell structure is determined for AgNi NPs, with oxidized silver atoms at the interface. - Abstract: The chemical structure of silver, nickel and bimetallic silver-nickel nanoparticles, i.e. Ag, Ni and AgNi NPs, with sizes {<=}35 nm, obtained by derived seed-mediated growth method on transparent and conductive indium tin oxide (ITO) substrates, has been studied by a comparative X-ray photoelectron spectroscopy (XPS) analysis of Ag 3d, Ni 2p and O1s core levels in combination with X-ray diffraction and optical absorption spectroscopy in the visible range. XPS indicates that the surface of Ag NPs is not oxidized, while Ni NPs are clearly oxidized to nickel oxide and hydroxide. Absorptions at 384 and 600 nm in Ni optical spectrum are consistent with the presence of nickel in oxidized state; however the presence of metallic Ni 2p signal in Ni XPS spectrum indicates that a metallic nickel core is still present. In the case of bimetallic AgNi NPs, the XPS results are consistent with the presence of metallic silver core surrounded by NiO + Ni(OH){sub 2} shell. XPS spectra also show the presence of Ag{sub 2}O at the interface between the Ag metallic core and the oxidized nickel shell. XRD patterns of AgNi and Ag NPs show the typical fcc structure of metallic silver, confirming the presence of Ag metallic core in AgNi NPs. The surface plasmon

  3. Hydrogen adsorption on bimetallic PdAu(111) surface alloys

    DEFF Research Database (Denmark)

    Takehiro, Naoki; Liu, Ping; Bergbreiter, Andreas

    2014-01-01

    The adsorption of hydrogen on structurally well defined PdAu-Pd(111) monolayer surface alloys was investigated in a combined experimental and theoretical study, aiming at a quantitative understanding of the adsorption and desorption properties of individual PdAu nanostructures. Combining...... the structural information obtained by high resolution scanning tunneling microscopy (STM), in particular on the abundance of specific adsorption ensembles at different Pd surface concentrations, with information on the adsorption properties derived from temperature programmed desorption (TPD) spectroscopy...... and high resolution electron energy loss spectroscopy (HREELS) provides conclusions on the minimum ensemble size for dissociative adsorption of hydrogen and on the adsorption energies on different sites active for adsorption. Density functional theory (DFT) based calculations give detailed insight...

  4. Unearthing a Well-Defined Highly Active Bimetallic W/Ti Precatalyst Anchored on a Single Silica Surface for Metathesis of Propane

    KAUST Repository

    Samantaray, Manoja

    2017-02-10

    Two compatible organometallic complexes, W(Me)(6) (1) and TiNp4 (2), were successively anchored on a highly dehydroxylated single silica support (SiO2-700) to synthesize the well-defined bimetallic precatalyst [(equivalent to Si-O-)W(Me)(5)(equivalent to Si-O-)Ti(Np)(3)] (4). Precatalyst 4 was characterized at the molecular level using advanced surface organometallic chemistry (SOMC) characterization techniques. The strong autocorrelation observed between methyl of W and Ti in H-1-H-1 multiple-quantum NMR spectra demonstrates that W and Ti species are in close proximity to each other. The bimetallic precatalyst 4, with a turnover number (TON) of 9784, proved to be significantly more efficient than the silica-supported monometallic catalyst [(equivalent to Si-O-)W(Me)(5)] (3), with a TON of 98, for propane metathesis at 150 degrees C in a flow reactor. The dramatic improvement in the activity signifies the cooperativity between Ti and W and indicates that the key step of alkane metathesis (C-H bond activation followed by beta-H elimination) occurs on Ti, followed by olefin metathesis, which occurs on W. We have demonstrated the influence and importance of proximity of Ti to W for achieving such a significantly high activity. This is the first report demonstrating the considerably high activity (TON = 9784) in propane metathesis at moderate temperature (150 degrees C) using a well-defined bimetallic system prepared via the SOMC approach.

  5. Surface Plasmon Resonance from Bimetallic Interface in Au–Ag Core–Shell Structure Nanowires

    Directory of Open Access Journals (Sweden)

    Zhu Jian

    2009-01-01

    Full Text Available Abstract Transverse surface plasmon resonances (SPR in Au–Ag and Ag–Au core–shell structure nanowires have been investigated by means of quasi-static theory. There are two kinds of SPR bands resulting from the outer surface of wall metal and the interface between core and wall metals, respectively. The SPR corresponding to the interface, which is similar to that of alloy particle, decreases and shifts obviously with increasing the wall thickness. However, the SPR corresponding to the outer surface, which is similar to that of pure metal particle, increases and shifts slightly with increasing the wall thickness. A mechanism based on oscillatory surface electrons under coulombic attraction is developed to illuminate the shift fashion of SPR from bimetallic core–shell interface. The net charges and extra coulombic force in metallic wall affect the SPR energy and the shift fashion.

  6. Preparation of highly dispersed Ru-Sn bimetallic supported catalysts from the single source precursors Cp(PPh32Ru-SnX3 (X = Cl or Br

    Directory of Open Access Journals (Sweden)

    Ana Cláudia Bernardes Silva

    2003-06-01

    Full Text Available In this work highly dispersed Ru-Sn bimetallic catalysts have been prepared from organobimetallic Cp(PPh32Ru-SnX3 (X = Cl or Br complexes. These single source precursors can be easily impregnated in high surface area supports, such as activated carbon and sol-gel SiO2, and upon controlled thermal treatment the ligands are released as volatile products resulting in the formation of the bimetallic system Ru-Sn. Catalytic reactions, such as hydrodechlorination of CCl4 and chlorobenzene and TPR (Temperature Programmed Reduction experiments carried out with these RuSn catalysts suggested a strong interaction between Ruthenium and Tin. Mössbauer measurements showed that these materials when exposed to air are immediately oxidized to form Sn (IV. It was shown that upon controlled reduction conditions with H2 it is possible to reduce selectively Sn to different oxidation states and different phases. The Sn oxidation state showed significant effect on the catalytic hydrogenation of 1,5-cyclooctadiene. The use of these single source precursors with a controlled decomposition/reduction procedure allows the preparation of unique catalysts with an intimate interaction between the components ruthenium and tin and the possibility of varying the Sn oxidation state around the Ru metal.

  7. Surface-Bound Ligands Modulate Chemoselectivity and Activity of a Bimetallic Nanoparticle Catalyst

    KAUST Repository

    Vu, Khanh B.

    2015-04-03

    "Naked" metal nanoparticles (NPs) are thermodynamically and kinetically unstable in solution. Ligands, surfactants, or polymers, which adsorb at a particle\\'s surface, can be used to stabilize NPs; however, such a mode of stabilization is undesirable for catalytic applications because the adsorbates block the surface active sites. The catalytic activity and the stability of NPs are usually inversely correlated. Here, we describe an example of a bimetallic (PtFe) NP catalyst stabilized by carboxylate surface ligands that bind preferentially to one of the metals (Fe). NPs stabilized by fluorous ligands were found to be remarkably competent in catalyzing the hydrogenation of cinnamaldehyde; NPs stabilized by hydrocarbon ligands were significantly less active. The chain length of the fluorous ligands played a key role in determining the chemoselectivity of the FePt NP catalysts. (Chemical Presented). © 2015 American Chemical Society.

  8. Bimetallic Catalysts and Platinum Surfaces Studied by X-ray Absorption Spectroscopy and Scanning Tunnelling Microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Roenning, Magnus

    2000-07-01

    Bimetallic catalyst systems used in Fischer-Tropsch synthesis (Co-Re/Al{sub 2}O{sub 3}) and in the naphtha reforming process (Pt-Re/Al{sub 2}O{sub 3}) have been studied in situ using X-ray absorption spectroscopy (EXAFS). Additionally, the adsorption of ethene on platinum single crystal surfaces has been investigated using scanning tunnelling microscopy. In situ EXAFS at the cobalt K absorption edge have been carried out at 450{sup o}C on the hydrogen reduction of a rhenium-promoted Co{sub 3}O{sub 4}/Al{sub 2}O{sub 3} catalyst. Reductions carried out using 100% hydrogen and 5% hydrogen in helium gave different results. Whereas the reduction using dilute hydrogen leads to bulk-like metallic cobalt particles (hcp or fcc), reaction with pure hydrogen yields a more dispersed system with smaller cobalt metal particles (< 40 A). The results are rationalised in terms of different degrees of reoxidation of cobalt by the higher and lower concentrations of water generated during the reduction of cobalt oxide by 100% and 5% hydrogen, respectively. Additionally, in both reduction protocols a small fraction (3 -4 wt%) of the cobalt content is randomly dispersed over the tetrahedral vacancies of the alumina support. This dispersion occurs during reduction and not calcination. The cobalt in these sites cannot be reduced at 450 {sup o}C. The local environments about the rhenium atoms in Co-Re/{gamma}-A1{sub 2}O{sub 3} catalyst after different reduction periods have been studied by X-ray absorption spectroscopy. A bimetallic catalyst containing 4.6 wt% cobalt and 2 wt% rhenium has been compared with a corresponding monometallic sample with 2 wt% rhenium on the same support. The rhenium L{sub III} EXAFS analysis shows that bimetallic particles are formed after reduction at 450{sup o}C with the average particle size being 10-15 A. Rhenium is shown to be reduced at a later stage than cobalt. The fraction of cobalt atoms entering the support obstructs the access to the support for the

  9. Preparation and catalytic activities for H{sub 2}O{sub 2} decomposition of Rh/Au bimetallic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Haijun, E-mail: zhanghaijun@wust.edu.cn [Key Laboratory of Integrated Exploitation of Bayan Obo Multi-Metal Resources, Inner Mongolia University of Science and Technology, Baotou 014010 (China); The State Key Laboratory of Refractory and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081 (China); Deng, Xiangong; Jiao, Chengpeng; Lu, Lilin; Zhang, Shaowei [The State Key Laboratory of Refractory and Metallurgy, Wuhan University of Science and Technology, Wuhan 430081 (China)

    2016-07-15

    Graphical abstract: PVP-protected Rh/Au bimetallic nanoparticles (BNPs) were prepared by using hydrogen sacrificial reduction method, the activity of Rh80Au20 BNPs were about 3.6 times higher than that of Rh NPs. - Highlights: • Rh/Au bimetallic nanoparticles (BNPs) of 3∼5 nm in diameter were prepared. • Activity for H{sub 2}O{sub 2} decomposition of BNPs is 3.6 times higher than that of Rh NPs. • The high activity of BNPs was caused by the existence of charged Rh atoms. • The apparent activation energy for H{sub 2}O{sub 2} decomposition over the BNPs was calculated. - Abstract: PVP-protected Rh/Au bimetallic nanoparticles (BNPs) were prepared by using hydrogen sacrificial reduction method and characterized by UV–vis, XRD, FT-IR, XPS, TEM, HR-TEM and DF-STEM, the effects of composition on their particle sizes and catalytic activities for H{sub 2}O{sub 2} decomposition were also studied. The as-prepared Rh/Au BNPs possessed a high catalytic activity for the H{sub 2}O{sub 2} decomposition, and the activity of the Rh{sub 80}Au{sub 20} BNPs with average size of 2.7 nm were about 3.6 times higher than that of Rh monometallic nanoparticles (MNPs) even the Rh MNPs possess a smaller particle size of 1.7 nm. In contrast, Au MNPs with size of 2.7 nm show no any activity. Density functional theory (DFT) calculation as well as XPS results showed that charged Rh and Au atoms formed via electronic charge transfer effects could be responsible for the high catalytic activity of the BNPs.

  10. Bimetallic Catalysts and Platinum Surfaces Studied by X-ray Absorption Spectroscopy and Scanning Tunnelling Microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Roenning, Magnus

    2000-07-01

    Bimetallic catalyst systems used in Fischer-Tropsch synthesis (Co-Re/Al{sub 2}O{sub 3}) and in the naphtha reforming process (Pt-Re/Al{sub 2}O{sub 3}) have been studied in situ using X-ray absorption spectroscopy (EXAFS). Additionally, the adsorption of ethene on platinum single crystal surfaces has been investigated using scanning tunnelling microscopy. In situ EXAFS at the cobalt K absorption edge have been carried out at 450{sup o}C on the hydrogen reduction of a rhenium-promoted Co{sub 3}O{sub 4}/Al{sub 2}O{sub 3} catalyst. Reductions carried out using 100% hydrogen and 5% hydrogen in helium gave different results. Whereas the reduction using dilute hydrogen leads to bulk-like metallic cobalt particles (hcp or fcc), reaction with pure hydrogen yields a more dispersed system with smaller cobalt metal particles (< 40 A). The results are rationalised in terms of different degrees of reoxidation of cobalt by the higher and lower concentrations of water generated during the reduction of cobalt oxide by 100% and 5% hydrogen, respectively. Additionally, in both reduction protocols a small fraction (3 -4 wt%) of the cobalt content is randomly dispersed over the tetrahedral vacancies of the alumina support. This dispersion occurs during reduction and not calcination. The cobalt in these sites cannot be reduced at 450 {sup o}C. The local environments about the rhenium atoms in Co-Re/{gamma}-A1{sub 2}O{sub 3} catalyst after different reduction periods have been studied by X-ray absorption spectroscopy. A bimetallic catalyst containing 4.6 wt% cobalt and 2 wt% rhenium has been compared with a corresponding monometallic sample with 2 wt% rhenium on the same support. The rhenium L{sub III} EXAFS analysis shows that bimetallic particles are formed after reduction at 450{sup o}C with the average particle size being 10-15 A. Rhenium is shown to be reduced at a later stage than cobalt. The fraction of cobalt atoms entering the support obstructs the access to the support for the

  11. Surface structure and reaction performances of highly dispersed and supported bimetallic catalysts

    Institute of Scientific and Technical Information of China (English)

    林励吾; 杨维慎; 贾继飞; 徐竹生; 张涛; 范以宁; 寇元; 沈俭一

    1999-01-01

    Surface structures of Pt-Sn and Pt-Fe bimetallic catalysts have been investigated by means of Mssbauer spectroscopy, Pt-LⅢ-edge EXAFS and H2-adsorption. The results showed that the second component, such as Sn or Fe, remained in the oxidative state and dispersed on the γ-Al2O3 surface after reduction, while Pt was completely reduced to the metallic state and dispersed on either the metal oxide surface or the γ-Al2O3 surface. By correlating the distribution of Pt species on different surfaces with the reaction and adsorption performances, it is proposed that two kinds of active Pt species existed on the surfaces of both catalysts, named M1 sites and M2 sites. M1 sites are the sites in which Pt directly anchored on the γ-Al2O3 surface, while M2 sites are those in which Pt anchored on the metal oxide surface. M1 sites are favorable for low temperature H2 adsorption, and responsible for the hydrogenolysis reaction and carbon deposition, while M2 sites which adsorb more H2 at higher tem

  12. Analysis of Manufacturing Bimetallic Tubes by the Cold Drawing Process

    Directory of Open Access Journals (Sweden)

    Halaczek D.

    2016-03-01

    Full Text Available Drawing processes apply to obtain the bimetallic tubes from the different metals and alloys, combined in the solid state, which significantly affects the specificity of this process. The manufacturing of bimetallic tubes by drawing process depends on many factors which include: preparation of the surface of materials joined in the solid state, the geometric parameters of the working tool, technological parameters of the drawing process (drawing speed, type of lubricant, the use of back pull etc.. Generally, the cold drawing process of producing the bimetallic tubes refers to metals which have high ductility (copper, aluminum, etc.. The tube sinking (tube drawing without a mandrel of bimetallic tubes together with joining them at the interface of the two metal in the solid-state is applied for tubes of the diameter range between 6 to 20 mm and based on of the reducing the diameter of the tube. However, a slight increase of wall thickness ca. 0.05 ÷ 0.10 mm can appear, which is not dangerous phenomenon in case of producing the bimetallic tubes by joining in the solid-state. The aim of the research was to investigate the technology of tubes drawing process from non-ferrous metal, drawing process of bimetallic tubes and the production of bimetallic tubes in layers composition: cooper Cu-ETP - brass CuZn37 and CuZn37 brass - copper Cu-ETP in the tube sinking process. The research program included: production of bimetallic tubes with a different composition (Cu- ETP-CuZn37 and CuZn37-Cu-ETP and a different percentage of the cross-section components; analysis of changes of tube wall thickness and the layer composition of the bimetallic tube, based on measurements on the workshop microscope; analysis of the material flow in the process of the bimetallic tubes production based on the measurements results of a profilograph CP-200.

  13. Tailoring the carbon nanostructures grown on the surface of Ni-Al bimetallic nanoparticles in the gas phase.

    Science.gov (United States)

    Kim, Whi Dong; Ahn, Ji Young; Lee, Dong Geun; Lee, Hyung Woo; Hong, Suck Won; Park, Hyun Seol; Kim, Soo H

    2011-10-15

    A gas-phase, one-step method for producing various aerosol carbon nanostructures is described. The carbon nanostructures can be selectively tailored with either straight, coiled, or sea urchin-like structures by controlling the size of Ni-Al bimetallic nanoparticles and the reaction temperature. The carbon nanostructures were grown using both conventional spray pyrolysis and thermal chemical vapor deposition. Bimetallic nanoparticles with catalytic Ni (guest) and non-catalytic Al (host) matrix were reacted with acetylene and hydrogen gases. At the processing temperature range of 650-800 °C, high concentration straight carbon nanotubes (S-CNTs) with a small amount of coiled carbon nanotubes (C-CNTs) can be grown on the surface of seeded bimetallic nanoparticle size 100 nm, resulting from the significant size reduction of the available Ni sites due to thermal expansion of molten Al matrix sites without consumption of Al matrix. However, at the processing temperature range of 500-650 °C, C-CNTs can be grown on the bimetallic nanoparticle size 100 nm due to the isolation of Ni sites in the Al matrix. Copyright © 2011 Elsevier Inc. All rights reserved.

  14. Probing the electronic and catalytic properties of a bimetallic surface with 3 nm resolution

    Science.gov (United States)

    Zhong, Jin-Hui; Jin, Xi; Meng, Lingyan; Wang, Xiang; Su, Hai-Sheng; Yang, Zhi-Lin; Williams, Christopher T.; Ren, Bin

    2016-11-01

    An atomic- and molecular-level understanding of heterogeneous catalysis is required to characterize the nature of active sites and improve the rational design of catalysts. Achieving this level of characterization requires techniques that can correlate catalytic performances to specific surface structures, so as to avoid averaging effects. Tip-enhanced Raman spectroscopy combines scanning probe microscopy with plasmon-enhanced Raman scattering and provides simultaneous topographical and chemical information at the nano/atomic scale from ambient to ultrahigh-vacuum and electrochemical environments. Therefore, it has been used to monitor catalytic reactions and is proposed to correlate the local structure and function of heterogeneous catalysts. Bimetallic catalysts, such as Pd-Au, show superior performance in various catalytic reactions, but it has remained challenging to correlate structure and reactivity because of their structural complexity. Here, we show that TERS can chemically and spatially probe the site-specific chemical (electronic and catalytic) and physical (plasmonic) properties of an atomically well-defined Pd(sub-monolayer)/Au(111) bimetallic model catalyst at 3 nm resolution in real space using phenyl isocyanide as a probe molecule (Fig. 1a). We observe a weakened N≡C bond and enhanced reactivity of phenyl isocyanide adsorbed at the Pd step edge compared with that at the Pd terrace. Density functional theory corroborates these observations by revealing a higher d-band electronic profile for the low-coordinated Pd step edge atoms. The 3 nm spatial resolution we demonstrate here is the result of an enhanced electric field and distinct electronic properties at the step edges.

  15. Selective hydrogen production from formic acid decomposition on Pd-Au bimetallic surfaces.

    Science.gov (United States)

    Yu, Wen-Yueh; Mullen, Gregory M; Flaherty, David W; Mullins, C Buddie

    2014-08-06

    Pd-Au catalysts have shown exceptional performance for selective hydrogen production via HCOOH decomposition, a promising alternative to solve issues associated with hydrogen storage and distribution. In this study, we utilized temperature-programmed desorption (TPD) and reactive molecular beam scattering (RMBS) in an attempt to unravel the factors governing the catalytic properties of Pd-Au bimetallic surfaces for HCOOH decomposition. Our results show that Pd atoms at the Pd-Au surface are responsible for activating HCOOH molecules; however, the selectivity of the reaction is dictated by the identity of the surface metal atoms adjacent to the Pd atoms. Pd atoms that reside at Pd-Au interface sites tend to favor dehydrogenation of HCOOH, whereas Pd atoms in Pd(111)-like sites, which lack neighboring Au atoms, favor dehydration of HCOOH. These observations suggest that the reactivity and selectivity of HCOOH decomposition on Pd-Au catalysts can be tailored by controlling the arrangement of surface Pd and Au atoms. The findings in this study may prove informative for rational design of Pd-Au catalysts for associated reactions including selective HCOOH decomposition for hydrogen production and electro-oxidation of HCOOH in the direct formic acid fuel cell.

  16. Self-organization of bimetallic PdAu nanoparticles on SiO{sub 2} surface

    Energy Technology Data Exchange (ETDEWEB)

    Ruffino, F., E-mail: francesco.ruffino@ct.infn.it; Grimaldi, M. G. [Universita di Catania, Dipartimento di Fisica e Astronomia (Italy)

    2011-06-15

    Bimetallic PdAu nanoparticles on SiO{sub 2} substrate were produced by a sequential room-temperature sputtering deposition method. By the atomic force microscopy technique we studied the nanoparticles self-organization mechanisms in various conditions. First, Pd nucleation and growth proceeds at the substrate defects and the Pd nanoparticles density increase rapidly. During the second sputtering deposition, Au atoms adsorb on the SiO{sub 2} and diffuse toward Pd nanoparticles without forming new nuclei. The Au atoms are trapped by the preformed Pd nanoparticles, forming PdAu bimetallic nanoparticles which size increases. Furthermore, fixing the amount of deposited Pd and increasing the amount of deposited Au, we analyzed the evolution of the PdAu film surface morphology: we observe that the PdAu grows initially as three-dimensional islands; then the PdAu film morphology evolves from compact three-dimensional islands to partially coalesced worm-like structures, followed by a percolation morphology and finally to a continuous and rough film. The application of the interrupted coalescence model allowed us to evaluate the critical mean island diameter R{sub c} Almost-Equal-To 2.8 nm for the partial coalescence process. The application of the dynamic scaling theory of growing interfaces allowed us to evaluate the dynamic growth exponent {beta} = 0.21 {+-} 0.01 from the evolution of the film surface roughness. Finally, fixing the amount of deposited Pd and Au we studied the self-organization mechanism of the PdAu nanoparticles induced by thermal processes performed in the 973-1173 K temperature range. The observed kinetic growth mechanism is consistent with a surface diffusion-limited ripening of the nanoparticles with a temperature-dependent growth exponent. The dependence of the growth exponent on the temperature is supposed to be linked to the variation with the temperature of the characteristics of the PdAu alloy. The activation energy for the surface diffusion

  17. Preparation of Bimetallic PtnPdm Supported Clusters with Well-Defined Stoichiometry

    Science.gov (United States)

    Rousset, J. L.; Cadrot, A. M.; Aires, F. Santos; Renouprez, A.; Mélinon, P.; Perez, A.; Pellarin, M.; Vialle, J. L.; Broyer, M.

    Supported bimetallic Pd-Pt clusters with a well-defined stoichiometry are produced using a laser-vaporization source. Free clusters are also studied by time-of-flight mass spectrometry and photofragmentation. The supported clusters are characterized by energy dispersive x-ray analysis. The low binding energy of palladium atoms compared to that of platinum is clearly demonstrated in both free and supported clusters. The reactivity is briefly discussed.

  18. Bimetallic nickel-iron nanoparticles for groundwater decontamination: effect of groundwater constituents on surface deactivation.

    Science.gov (United States)

    Han, Yanlai; Yan, Weile

    2014-12-01

    The incorporation of catalytic metals on iron nanoparticles to form bimetallic nanoparticles (BNPs) generates a class of highly reactive materials for degrading chlorinated hydrocarbons (e.g., trichloroethylene, TCE) in groundwater. Successful implementation of BNPs to groundwater decontamination relies critically on the stability of surface reactive sites of BNPs in groundwater matrices. This study investigated the effect of common groundwater solutes on TCE reduction with Ni-Fe (with Ni at 2 wt.%) bimetallic nanoparticles (herein denoted as Ni-Fe BNPs). Batch experiments involving pre-exposing the nanoparticles to various groundwater solutions for 24 h followed by reactions with TCE solutions were conducted. The results suggest that the deactivation behavior of Ni-Fe BNPs differs significantly from that of the well-studied Pd-Fe BNPs. Specifically, Ni-Fe BNPs were chemically stable in pure water. Mild reduction in TCE reaction rates were observed for Ni-Fe BNPs pre-exposed to chloride (Cl(-)), bicarbonate (HCO3(-)), sulfite (SO3(2-)) and humic acid solutions. Nitrate (NO3(-)), sulfate (SO4(2-)) and phosphate (HPO4(2-)) may cause moderate to severe deactivation at elevated concentrations (>1 mM). Product analysis and surface chemistry investigations using high-resolution X-ray photoelectron spectroscopy (HR-XPS) reveal that NO3(-) decreased particle reactivity mainly due to progressive formation of passivating oxides, whereas SO4(2-) and phosphate elicited rapid deactivation as a result of specific poisoning of the surface nickel sites. At similar levels, phosphate is the most potent deactivation agent among the solutes examined in this study. While our findings point out the desirable quality of Ni-Fe nanoparticles, particularly their greater electrochemical stability compared to Pd-Fe BNPs, its susceptibility to chemical poisoning at high levels of complexing ligands is also noted. Groundwater chemistry is therefore an important factor to consider when

  19. Study of Ag induced bimetallic (Au-Ag) nanowires on silicon (5 5 12) surfaces: Experiment and theoretical aspects

    Science.gov (United States)

    Bhukta, Anjan; Bagarti, Trilochan; Guha, Puspendu; Ravulapalli, Sathyavathi; Satpati, Biswarup; Rakshit, Bipul; Maiti, Paramita; Parlapalli, Venkata Satyam

    2017-10-01

    The reconstructed vicinal (high index) silicon surfaces, such as, Si (5 5 12) composes row-like structures that can be used as templates for growing aligned nanowires. By using a sub-monolayers of Ag, prior to Au deposition on reconstructed Si (5 512) surface, intermixing of Au and Ag, enhancement of aspect ratio of bimetallic Au-Ag nanowires with tunable morphology is reported. This is attributed to a combined effect of pre-grown Ag strips as nucleation centers for incoming Au ad-atoms and anisotropic Au-Ag intermixing. To achieve optimum conditions for the growth of larger aspect ratio Au-Ag nanostructures, the growth kinetics have been studied by varying growth and annealing temperatures. At ≈400 °C, the Ag diffused into silicon substrate and the inter-diffusion found to inhibit the formation of Au-Ag bimetallic nanostructures. Controlled experiments under ultra-high vacuum condition in a molecular beam epitaxy system and in-situ scanning tunneling microscopy measurements along with ex-situ scanning transmission and secondary electron microscopy measurements have been carried out to understand the bimetallic nanostructure growth. Kinetic Monte Carlo (KMC) simulations based on kinematics of ad-atoms on an anisotropic template with a solid on solid model in which the relative ratios of binding energies (that are obtained from the Density Functional Theory) have been used and the KMC simulations results agree with the experimental observations. Advantage of having bimetallic structures as effective substrates for Surface enhanced Raman spectroscopy application is demonstrated by detecting Rhodamine 6 G (R6G) molecule at the concentration of 10-7M.

  20. Alloy formation and chemisorption at Zn/Pt(111) bimetallic surfaces using alkali ISS, XPD, and TPD.

    Science.gov (United States)

    Ho, Chih-Sung; Martono, Eddie; Banerjee, Santanu; Roszell, John; Vohs, John; Koel, Bruce E

    2013-11-21

    Alloy formation and chemisorption at bimetallic surfaces formed by vapor-depositing Zn on a Pt(111) single crystal were investigated primarily by using X-ray photoelectron diffraction (XPD), X-ray photoelectron spectroscopy (XPS), low-energy alkali ion scattering spectroscopy (ALISS), low electron energy diffraction (LEED), and temperature programmed desorption (TPD). A wide range of conditions were investigated to explore whether deposition and annealing of Zn films could produce well-defined, ordered alloy surfaces, similar to those encountered for Sn/Pt(111) surface alloys. These attempts were unsuccessful, although weak, diffuse (2 × 2) spots were observed under special conditions. The particular PtZn bimetallic alloy created by annealing one monolayer of Zn on Pt(111) at 600 K, which has a Zn composition in the surface layer of about 5 at. %, was investigated in detail by using XPD and ALISS. Only a diffuse (1 × 1) pattern was observed from this surface by LEED, suggesting that no long-range, ordered alloy structure was formed. Zn atoms were substitutionally incorporated into the Pt(111) crystal to form a near-surface alloy in which Zn atoms were found to reside primarily in the topmost and second layers. The alloyed Zn atoms in the topmost layer are coplanar with the Pt atoms in the surface layer, without any "buckling" of Zn, that is, displacement in the vertical direction. This result is expected because of the similar size of Pt and Zn, based on previous studies of bimetallic Pt alloys. Zn atoms desorb upon heating rather than diffusing deep into the bulk of the Pt crystal. Temperature programmed desorption (TPD) measurements show that both CO and NO have lower desorption energies on the PtZn alloy surface compared to that on the clean Pt(111) surface.

  1. Preparation of Rh/Ni Bimetallic Nanoparticles and Their Catalytic Activities for Hydrogen Generation from Hydrolysis of KBH4

    Directory of Open Access Journals (Sweden)

    Liqiong Wang

    2017-04-01

    Full Text Available ISOBAM–104 protected Rh/Ni bimetallic nanoparticles (BNPs of 3.1 nm in diameter were synthesized by a co–reduction method with a rapid injection of KBH4 solution. The catalytic activities of as–prepared BNPs for hydrogen generation from hydrolysis of a basic KBH4 solution were evaluated. Ultraviolet–visible spectrophotometry (UV–Vis, transmission electron microscopy (TEM, and high–resolution transmission electron microscopy (HRTEM were employed to characterize the structure, particle size, and chemical composition of the resultant BNPs. Catalytic activities for hydrolysis of KBH4 and catalytic kinetics of prepared BNPs were also investigated. It was shown that Rh/Ni BNPs displayed much higher catalytic activities than that of Rh or Ni monometallic nanoparticles (MNPs, and the prepared Rh10Ni90 BNPs possessed the highest catalytic activities with a value of 11580 mol–H2·h−1·mol–Rh−1. The high catalytic activities of Rh/Ni BNPs could be attributed to the electron transfer effect between Rh and Ni atoms, which was confirmed by a density functional theory (DFT calculation. The apparent activation energy for hydrogen generation of the prepared Rh10Ni90 BNPs was about 47.2 ± 2.1kJ/mol according to a kinetic study.

  2. Synthesis and Electrochemical Evaluation of Carbon Supported Pt-Co Bimetallic Catalysts Prepared by Electroless Deposition and Modified Charge Enhanced Dry Impregnation

    Directory of Open Access Journals (Sweden)

    John Meynard M. Tengco

    2016-06-01

    Full Text Available Carbon-supported bimetallic Pt-Co cathode catalysts have been previously identified as higher activity alternatives to conventional Pt/C catalysts for fuel cells. In this work, a series of Pt-Co/C catalysts were synthesized using electroless deposition (ED of Pt on a Co/C catalyst prepared by modified charge enhanced dry impregnation. X-ray diffraction (XRD and scanning transmission electron microscopy (STEM characterization of the base catalyst showed highly dispersed particles. A basic ED bath containing PtCl62− as the Pt precursor, dimethylamine borane as reducing agent, and ethylenediamine as stabilizing agent successfully targeted deposition of Pt on Co particles. Simultaneous action of galvanic displacement and ED resulted in Pt-Co alloy formation observed in XRD and energy dispersive X-ray spectroscopy (XEDS mapping. In addition, fast deposition kinetics resulted in hollow shell Pt-Co alloy particles while particles with Pt-rich shell and Co-rich cores formed with controlled Pt deposition. Electrochemical evaluation of the Pt-Co/C catalysts showed lower active surface but much higher mass and surface activities for oxygen reduction reaction compared to a commercial Pt/C fuel cell catalyst.

  3. Synthesis and Electrochemical Evaluation of Carbon Supported Pt-Co Bimetallic Catalysts Prepared by Electroless Deposition and Modified Charge Enhanced Dry Impregnation

    OpenAIRE

    John Meynard M. Tengco; Bahareh Alsadat Tavakoli Mehrabadi; Yunya Zhang; Akkarat Wongkaew; John R. Regalbuto; Weidner, John W.; John R. Monnier

    2016-01-01

    Carbon-supported bimetallic Pt-Co cathode catalysts have been previously identified as higher activity alternatives to conventional Pt/C catalysts for fuel cells. In this work, a series of Pt-Co/C catalysts were synthesized using electroless deposition (ED) of Pt on a Co/C catalyst prepared by modified charge enhanced dry impregnation. X-ray diffraction (XRD) and scanning transmission electron microscopy (STEM) characterization of the base catalyst showed highly dispersed particles. A basic E...

  4. 离子掩蔽剂在制备铜银双金属粉中的应用%Ionic Masking Agent in the Preparation of Copper-Silver Bimetallic Powder

    Institute of Scientific and Technical Information of China (English)

    彭优; 聂登攀; 薛涛

    2011-01-01

    采用化学置换法制备了系列铜银双金属粉,在制备过程中添加离子掩蔽剂,有效消除了铜氨络合离子在铜粉表面的吸附,实现银在铜粉表面的连续包覆.分析了掩蔽原理及其主要影响因素,并用透射电子显微镜,热重分析仪,X射线衍射仪对铜银双金属粉进行了表征.结果表明:在添加了离子掩蔽剂后制备铜银双金属粉末为连续包覆型结构,分散性好,有效改善了铜粉的抗氧化性能.%A series of copper-silver bimetallic powder was prepared by a chemical replacement method.In this process, ionic masking agent was added to eliminate copper ammonia complex ions adsorption on copper powder surface, which realizes silver continuous coating on the copper powder surfaces.The masking mechanism and the main influencing factors were analyzed.Besides that, TEM, TGA and XRD were used to characterize the Cu-Ag bimetallic powder.Results show that the copper-silver bimetallic powder with the ionic masking agent is of a continuous coating type structure, which has good dispersity, effectively improving antioxidation properties of the copper powdet.

  5. Preparation of Bimetallic Pd-Co Nanoparticles on Graphene Support for Use as Methanol Tolerant Oxygen Reduction Electrocatalysts

    Directory of Open Access Journals (Sweden)

    R. N. Singh

    2012-12-01

    Full Text Available Graphene-supported (40-x wt% Pd x wt% Co (0≤x≤13.33 alloys/composites have been prepared by a microwave-assisted polyol reduction method and been investigated for their structural and electrocatalytic properties for the oxygen reduction reaction (ORR in 0.5 M H2SO4 at 298 K. The study demonstrated that the bimetallic Pd-Co composite nanoparticles are, in fact, alloy nanoparticles with fcc crystalline structure. Partial substitution of Pd by Co (from 3.64 to 13.33 wt% in 40 wt% Pd/graphene decreases the lattice parameter as well as the crystallite size and increases the apparent catalytic activity, the latter, however, being the greatest with 8 wt% Co. The ORR activity of the active 32 wt% Pd 8wt% Co is found to be considerably low when it was deposited on the support multiwall carbon nanotubes under similar conditions. The rotating disk electrode study indicated that the ORR on 32 wt% Pd 8 wt% Co/GNS in 0.5 M H2SO4 follows approximately the four-electron pathway.

  6. Surface structure and relaxation during the oxidation of carbon monoxide on Pt Pd bimetallic surfaces

    Science.gov (United States)

    Lucas, C. A.; Markovic, N. M.; Ball, M.; Stamenkovic, V.; Climent, V.; Ross, P. N.

    2001-05-01

    The atomic structure and surface relaxation of Pd monolayer on Pt(1 1 1) has been studied by surface X-ray scattering, in an aqueous environment under electrostatic potential control, during the adsorption and oxidation of carbon monoxide. The results show that the Pd-Pt layer spacing contracts at the onset of CO oxidation before the Pd adlayer forms an oxide structure that is incommensurate with the Pt lattice. Both the oxide formation and the lattice contraction are fully reversible over many cycles of the applied electrode potential.

  7. Resolution Enhancement in Surface Plasmon Resonance Sensor Based on Waveguide Coupled Mode by Combining a Bimetallic Approach

    Directory of Open Access Journals (Sweden)

    Won Mok Kim

    2010-12-01

    Full Text Available In this study, we present and demonstrate a new route to a great enhancement in resolution of surface plasmon resonance sensors. Basically, our approach combines a waveguide coupled plasmonic mode and a kind of Au/Ag bimetallic enhancement concept. Theoretical modeling was carried out by solving Fresnel equations for the multilayer stack of prism/Ag inner-metal layer/dielectric waveguide/Au outer-metal layer. The inner Ag layer couples incident light to a guided wave and makes more fields effectively concentrated on the outer Au surface. A substantial enhancement in resolution was experimentally verified for the model stack using a ZnS-SiO2 waveguide layer.

  8. Colloidal synthesis and structural control of PtSn bimetallic nanoparticles.

    Science.gov (United States)

    Wang, Xiaodong; Stöver, Jörg; Zielasek, Volkmar; Altmann, Lena; Thiel, Karsten; Al-Shamery, Katharina; Bäumer, Marcus; Borchert, Holger; Parisi, Jürgen; Kolny-Olesiak, Joanna

    2011-09-06

    PtSn bimetallic nanoparticles with different particle sizes (1-9 nm), metal compositions (Sn content of 10-80 mol %), and organic capping agents (e.g., amine, thiol, carboxylic acid and polymer) were synthesized by colloidal chemistry methods. Transmission electron microscopy (TEM) measurements show that, depending on the particle size, the as-prepared bimetallic nanocrystals have quasi-spherical or faceted shapes. Energy-dispersive X-ray (EDX) analyses indicate that for all samples the signals of both Pt and Sn can be detected from single nanoparticles, confirming that the products are actually bimetallic but not only a physical mixture of pure Pt and Sn metal nanoparticles. X-ray diffraction (XRD) measurements were also conducted on the bimetallic particle systems. When compared with the diffraction patterns of monometallic Pt nanoparticles, the bimetallic samples show distinct shifts of the Bragg reflections to lower degrees, which gives clear proof of the alloying of Pt with Sn. However, a quantitative analysis of the lattice parameter shifts indicates that only part of the Sn atoms are incorporated into the alloy nanocrystals. This is consistent with X-ray photoelectron spectroscopy (XPS) measurements that reveal the segregation of Sn at the surfaces of the nanocrystals. Moreover, short PtSn bimetallic nanowires were synthesized by a seed-mediated growth method with amine-capped bimetallic particles as precursors. The resulting nanowires have an average width of 2.3 nm and lengths ranging from 5 to 20 nm. © 2011 American Chemical Society

  9. Surface structures and compositions of Au-Rh bimetallic nanoclusters supported on thin-film Al2O3/NiAl(100) probed with CO

    Science.gov (United States)

    Lee, Hsuan; Liao, Zhen-He; Hsu, Po-Wei; Hung, Ting-Chieh; Wu, Yu-Cheng; Lin, Yuwei; Wang, Jeng-Han; Luo, Meng-Fan

    2017-07-01

    The surface structures and compositions of Au-Rh bimetallic nanoclusters on an ordered thin film of Al2O3/NiAl(100) were investigated, primarily with infrared reflection absorption spectra and temperature-programmed desorption of CO as a probe molecule under ultrahigh-vacuum conditions and calculations based on density-functional theory. The bimetallic clusters were formed by sequential deposition of vapors of Au and Rh onto Al2O3/NiAl(100) at 300 K. Alloying in the clusters was active and proceeded toward a specific structure—a fcc phase, (100) orientation, and Rh core-Au shell structure, regardless of the order of metal deposition. For Au clusters incorporating deposited Rh, the Au atoms remained at the cluster surface through position exchange and became less coordinated; for deposition in reverse order, deposited Au simply decorated the surfaces of Rh clusters. Both adsorption energy and infrared absorption intensity were enhanced for CO on Au sites of the bimetallic clusters; both of them are associated with the bonding to Rh and also a decreased coordination number of CO-binding Au. These enhancements can thus serve as a fingerprint for alloying and atomic inter-diffusion in similar bimetallic systems.

  10. Surface-enhanced Raman scattering (SERS)-based volatile organic compounds (VOCs) detection using plasmonic bimetallic nanogap substrate

    DEFF Research Database (Denmark)

    Wong, Chi Lok; Dinish, U. S.; Buddharaju, Kavitha Devi

    2014-01-01

    In this paper, we present surface-enhanced Raman scattering (SERS)-based volatile organic compounds (VOCs) detection with bimetallic nanogap structure substrate. Deep UV photolithography at the wavelength of 250 nm is used to pattern circular shape nanostructures. The nanogap between adjacent....... The measurement results are found reproducible, and the detection limit is found to be 9.5 pg (acetone molecule). The detection sensitivity is 28.7 % higher than that of the recent reported leaning silicon nanopillar substrate. With further system miniaturization, the sensing technique can work as a portable SERS...... circular patterns is 30 +/- 5 nm. Silver (30 nm) and gold (15 nm) plasmonic active layers are deposited on the nanostructures subsequently. SERS measurements on different concentrations of acetone vapor ranged from 0.7, 1.5, 3.5, 10.3, 24.5 % and control have been performed with the substrate...

  11. Preparation of Au-Pd bimetallic nanoparticles in porous germania nanospheres: A study of their morphology and catalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Regan, Maureen R. [Department of Chemistry, Fordham University, 441, East Fordham Road, Bronx, NY 10458 (United States); Banerjee, Ipsita A. [Department of Chemistry, Fordham University, 441, East Fordham Road, Bronx, NY 10458 (United States)]. E-mail: banerjee@fordham.edu

    2006-03-15

    Size controlled Au-Pd bimetallic nanoparticles with an average size of 7-10 nm were grown in porous germania nanospheres. The properties of the resulting nanocomposites were characterized by electron microscopy, energy dispersive spectroscopy, and ultraviolet-visible spectroscopy. The catalytic activity of the nanocomposites was also examined by studying the degradation of p-nitroaniline.

  12. Preparation of Core-shell Cu-Ag Bimetallic Powder via Electroless Coating

    Institute of Scientific and Technical Information of China (English)

    XU Rui; ZHOU Kanggen; HU Minyi

    2009-01-01

    A novel method of electroless silver coating on copper powders was reported,in which hydrazine was used as the reducing agent,and had some advantages such was used as inhib-iting the substitution reaction and reducing consumption of copper powders.In the processes of sen-sitization and activation,AgNO_3 replaces the conventional PdCl_2,which solves the impurity of bath.Oxide film on the surface of copper powders was tested by chemical analysis.Ag element tested by XRD and XRF is in the form of Ag~0 and exists on the surface of copper powders,which acts as catalyzer in reduction reaction.Morphology and composition of the coating were characterized by SEM and XRD respectively.

  13. The use of mechanical alloying for the preparation of palladized magnesium bimetallic particles for the remediation of PCBs.

    Science.gov (United States)

    Coutts, Janelle L; Devor, Robert W; Aitken, Brian; Hampton, Michael D; Quinn, Jacqueline W; Clausen, Christian A; Geiger, Cherie L

    2011-09-15

    The kinetic rate of dechlorination of a polychlorinated biphenyl (PCB-151) by mechanically alloyed Mg/Pd was studied for optimization of the bimetallic system. Bimetal production was first carried out in a small-scale environment using a SPEX 8000M high-energy ball mill with 4-μm-magnesium and palladium impregnated on graphite, with optimized parameters including milling time and Pd-loading. A 5.57-g sample of bimetal containing 0.1257% Pd and ball milled for 3 min resulted in a degradation rate of 0.00176 min(-1)g(-1) catalyst as the most reactive bimetal. The process was then scaled-up, using a Red Devil 5400 Twin-Arm Paint Shaker, fitted with custom plates to hold milling canisters. Optimization parameters tested included milling time, number of ball bearings used, Pd-loading, and total bimetal mass milled. An 85-g sample of bimetal containing 0.1059% Pd and ball-milled for 23 min with 16 ball bearings yielded the most reactive bimetal with a degradation rate of 0.00122 min(-1)g(-1) catalyst. Further testing showed adsorption did not hinder extraction efficiency and that dechlorination products were only seen when using the bimetallic system, as opposed to any of its single components. The bimetallic system was also tested for its ability to degrade a second PCB congener, PCB-45, and a PCB mixture (Arochlor 1254); both contaminants were seen to degrade successfully.

  14. Catalysis on singly dispersed bimetallic sites

    Science.gov (United States)

    Zhang, Shiran; Nguyen, Luan; Liang, Jin-Xia; Shan, Junjun; Liu, Jingyue; Frenkel, Anatoly I.; Patlolla, Anitha; Huang, Weixin; Li, Jun; Tao, Franklin

    2015-08-01

    A catalytic site typically consists of one or more atoms of a catalyst surface that arrange into a configuration offering a specific electronic structure for adsorbing or dissociating reactant molecules. The catalytic activity of adjacent bimetallic sites of metallic nanoparticles has been studied previously. An isolated bimetallic site supported on a non-metallic surface could exhibit a distinctly different catalytic performance owing to the cationic state of the singly dispersed bimetallic site and the minimized choices of binding configurations of a reactant molecule compared with continuously packed bimetallic sites. Here we report that isolated Rh1Co3 bimetallic sites exhibit a distinctly different catalytic performance in reduction of nitric oxide with carbon monoxide at low temperature, resulting from strong adsorption of two nitric oxide molecules and a nitrous oxide intermediate on Rh1Co3 sites and following a low-barrier pathway dissociation to dinitrogen and an oxygen atom. This observation suggests a method to develop catalysts with high selectivity.

  15. Noble metal-based bimetallic nanoparticles: the effect of the structure on the optical, catalytic and photocatalytic properties.

    Science.gov (United States)

    Zaleska-Medynska, Adriana; Marchelek, Martyna; Diak, Magdalena; Grabowska, Ewelina

    2016-03-01

    Nanoparticles composed of two different metal elements show novel electronic, optical, catalytic or photocatalytic properties from monometallic nanoparticles. Bimetallic nanoparticles could show not only the combination of the properties related to the presence of two individual metals, but also new properties due to a synergy between two metals. The structure of bimetallic nanoparticles can be oriented in random alloy, alloy with an intermetallic compound, cluster-in-cluster or core-shell structures and is strictly dependent on the relative strengths of metal-metal bond, surface energies of bulk elements, relative atomic sizes, preparation method and conditions, etc. In this review, selected properties, such as structure, optical, catalytic and photocatalytic of noble metals-based bimetallic nanoparticles, are discussed together with preparation routes. The effects of preparation method conditions as well as metal properties on the final structure of bimetallic nanoparticles (from alloy to core-shell structure) are followed. The role of bimetallic nanoparticles in heterogeneous catalysis and photocatalysis are discussed. Furthermore, structure and optical characteristics of bimetallic nanoparticles are described in relation to the some features of monometallic NPs. Such a complex approach allows to systematize knowledge and to identify the future direction of research.

  16. Sonochemically preparation and characterization of bimetallic Ni-Co/Al2O3-ZrO2 nanocatalyst: Effects of ultrasound irradiation time and power on catalytic properties and activity in dry reforming of CH4.

    Science.gov (United States)

    Mahboob, Salar; Haghighi, Mohammad; Rahmani, Farhad

    2017-09-01

    The catalytic performance of nanostructured Ni-Co/Al2O3-ZrO2 catalysts, prepared by ultrasound-assisted impregnation method was examined in the dry reforming of methane. The effect of irradiation power and irradiation time have been studied by changing time (0, 20, 80min) and power of the sonication (30, 60, 90W) during the synthesis which resulted in different physiochemical properties of the nanocatalyst. The nanocatalysts were characterized by XRD, FESEM, PSD, EDX, TEM, TPR-H2, BET, FTIR and TG analyses. Based on the characterization results, ultrasound treatment endowed the sample with more uniform and smaller nanoparticles; higher surface area, stronger metal-support interaction and more homogenous dispersion. Moreover, the analyses exhibited smaller particles with higher surface area and less population of particle aggregates at longer and highly irradiated nanocatalysts. The nanocatalyst irradiated at 90W for 80min (the longest irradiation time and the most intense power) showed a uniform morphology and a very narrow particles size distribution. More than 65% of particles of this nanocatalyst were in the range of 10-30nm. Activity tests demonstrated that employing ultrasound irradiation during impregnation improves feed conversion and products yield, reaching values close to equilibrium. Among sonicated nanocatalysts, with increasing power and time of irradiation, the nanocatalyst represents higher activity. The superior performance amongst the various bimetallic catalysts tested was observed over the catalyst with 90W and 80min ultrasonic irradiation which is stable in 24h time on stream test. The excellent anti-coking performance of this bimetallic catalyst, confirmed by TG and FESEM analyses of spent catalyst, is closely related to the promoting effect of sonication on the metal-support interaction, Ni dispersion and particle size; and probably, the synergy between metallic species. Copyright © 2017 Elsevier B.V. All rights reserved.

  17. Method of surface preparation of niobium

    Science.gov (United States)

    Srinivasan-Rao, Triveni; Schill, John F.

    2003-01-01

    The present invention is for a method of preparing a surface of niobium. The preparation method includes polishing, cleaning, baking and irradiating the niobium surface whereby the resulting niobium surface has a high quantum efficiency.

  18. A first-principle calculation of sulfur oxidation on metallic Ni(111) and Pt(111), and bimetallic Ni@Pt(111) and Pt@Ni(111) surfaces.

    Science.gov (United States)

    Yeh, Chen-Hao; Ho, Jia-Jen

    2012-09-17

    Sulfur, a pollutant known to poison fuel-cell electrodes, generally comes from S-containing species such as hydrogen sulfide (H(2)S). The S-containing species become adsorbed on a metal electrode and leave atomic S strongly bound to the metal surface. This surface sulfur is completely removed typically by oxidation with O(2) into gaseous SO(2). According to our DFT calculations, the oxidation of sulfur at 0.25 ML surface sulfur coverage on pure Pt(111) and Ni(111) metal surfaces is exothermic. The barriers to the formation of SO(2) are 0.41 and 1.07 eV, respectively. Various metals combined to form bimetallic surfaces are reported to tune the catalytic capabilities toward some reactions. Our results show that it is more difficult to remove surface sulfur from a Ni@Pt(111) surface with reaction barrier 1.86 eV for SO(2) formation than from a Pt@Ni(111) surface (0.13 eV). This result is in good agreement with the statement that bimetallic surfaces could demonstrate more or less activity than to pure metal surfaces by comparing electronic and structural effects. Furthermore, by calculating the reaction free energies we found that the sulfur oxidation reaction on the Pt@Ni(111) surface exhibits the best spontaneity of SO(2) desorption at either room temperature or high temperatures.

  19. Mono- and bimetallic Rh and Pt NSR-catalysts prepared by controlled deposition of noble metals on support or storage component.

    Science.gov (United States)

    Büchel, Robert; Pratsinis, Sotiris E; Baiker, Alfons

    2012-02-22

    Mono- and bimetallic Rh and Pt based NOx storage-reduction (NSR) catalysts, where the noble metals were deposited on the Al2O3 support or BaCO3 storage component, have been prepared using a twin flame spray pyrolysis setup. The catalysts were characterized by nitrogen adsorption, CO chemisorption combined with diffuse reflectance infrared Fourier transform spectroscopy, X-ray diffraction, and scanning transmission electron microscopy combined with energy dispersive X-ray spectroscopy. The NSR performance of the catalysts was investigated by fuel lean/rich cycling in the absence and presence of SO2 (25 ppm) as well as after H2 desulfation at 750 °C. The performance increased when Rh was located on BaCO3 enabling good catalyst regeneration during the fuel rich phase. Best performance was observed for bimetallic catalysts where the noble metals were separated, with Pt on Al2O3 and Rh on BaCO3. The Rh-containing catalysts generally showed much higher tolerance to SO2 during fuel rich conditions and lost only little activity during thermal aging at 750 °C.

  20. Adsorption and dissociation of H2S on monometallic and monolayer bimetallic Ni/Pd(111) surfaces: A first-principles study

    Science.gov (United States)

    Li, Yi; Huang, Pan; Tao, Dandan; Wu, Juan; Qiu, Mei; Huang, Xin; Ding, Kaining; Chen, Wenkai; Su, Wenyue; Zhang, Yongfan

    2016-11-01

    Periodic density functional theory calculations have been performed to investigate the adsorption structures and dissociative reaction pathways for H2S molecule on Ni(111), Pd(111) and Ni/Pd(111) monolayer bimetallic surfaces with surface monolayer and subsurface monolayer structures. Our results indicate that, for the molecular adsorption mode, the introducing Pd atoms on Ni(111) can enhance the binding strength between H2S and the surface, while an opposite effect is achieved when the Ni monolayer is formed on Pd(111) surface. The decompositions of H2S molecule on all Ni/Pd(111) surfaces are exothermic, especially for the surfaces that the top layer is composed of Ni atoms. According to the predicted minimum energy paths that connect the molecular and dissociative states, two elementary steps are found for all Ni/Pd(111) metal surfaces, and the breaking of the first Hsbnd S bond is the rate-determining step for the H2S dissociation. Our results reveal that in most cases, the decomposition of H2S molecule on the monometallic and Ni/Pd(111) monolayer bimetallic surfaces is easy to happen. However, on the monolayer Ni-Pd(111) surface, there is a competition between the trapping-desorption channel and activated dissociation channel, which implies that depositing one monolayer Ni on a Pd(111) surface may help reducing sulfur poisoning by hindering the dissociation of H2S molecule.

  1. Crystalline structure-dependent growth of bimetallic nanostructures.

    Science.gov (United States)

    Li, Qian; Jiang, Ruibin; Ming, Tian; Fang, Caihong; Wang, Jianfang

    2012-11-21

    Morphological control of multimetallic nanostructures is crucial for obtaining shape-dependent physical and chemical properties. Up to date, control of the shapes of multimetallic nanostructures has remained largely empirical. Multimetallic nanostructures have been produced mostly through seed-mediated growth. Understanding the role played by starting nanocrystal seeds can help in controlling the shape and in turn the plasmonic and catalytic properties of multimetallic nanostructures. In this work, we have studied the effect of the crystalline structure and shape of Au nanocrystal seeds on the morphology of the resultant bimetallic nanostructures. Single-crystalline Au nanorods, multiply twinned Au nanorods, and multiply twinned Au nanobipyramids were employed as the starting seeds. Both silver and palladium exhibit highly preferential growth on the side surfaces of the single-crystalline Au nanorods, giving rise to bimetallic cuboids, whereas they prefer to grow at the ends of the multiply twinned Au nanorods and nanobipyramids, giving rise to bimetallic nanorods. These results indicate that the morphology of the bimetallic nanostructures is highly dependent on the crystalline structure of the Au nanocrystal seeds. Our results will be useful for guiding the preparation of multimetallic nanostructures with desired shapes and therefore plasmonic properties for various plasmon-based applications.

  2. Stellated Ag-Pt bimetallic nanoparticles: An effective platform for catalytic activity tuning

    Science.gov (United States)

    Liu, Hui; Ye, Feng; Yao, Qiaofeng; Cao, Hongbin; Xie, Jianping; Lee, Jim Yang; Yang, Jun

    2014-01-01

    The usefulness of Pt-based nanomaterials for catalysis can be greatly enhanced by coupling morphology engineering to the strategic presence of a second or even third metal. Here we demonstrate the design and preparation of stellated Ag-Pt bimetallic nanoparticles where significant activity difference between the methanol oxidation reaction (MOR) and the oxygen reduction reaction (ORR) may be realized by relegating Ag to the core or by hollowing out the core. In particular the stellated Pt surface, with an abundance of steps, edges, corner atoms, and {111} facets, is highly effective for the ORR but is ineffective for MOR. MOR activity is only observed in the presence of a Ag core through electronic coupling to the stellated Pt shell. The bimetallic Ag-Pt stellates therefore demonstrate the feasibility of tuning a Pt surface for two very different structure sensitive catalytic reactions. Stellated bimetallics may therefore be an effective platform for highly tunable catalyst designs. PMID:24495979

  3. Site-directed immobilization of antibody using EDC-NHS-activated protein A on a bimetallic-based surface plasmon resonance chip

    Science.gov (United States)

    Sohn, Young-Soo; Lee, Yeon Kyung

    2014-05-01

    The characteristics of a waveguide-coupled bimetallic surface plasmon resonance (WcBiM SPR) sensor using (3-dimethylaminopropyl)-3-ethylcarbodiimide(EDC)-N-hydroxysuccinimide(NHS)-activated protein A was investigated, and the detection of IgG using the EDC-NHS-activated protein A was studied in comparison with protein A and a self-assembled monolayer (SAM). The WcBiM sensor, which has a narrower full width at half maximum (FWHM) and a steeper slope, was selected since it leads to a larger change in the reflectance in the intensity detection mode. A preparation of the EDC-NHS-activated protein A for site-directed immobilization of antibodies was relative easily compared to the engineered protein G and A. In antigen-antibody interactions, the response to IgG at the concentrations of 50, 100, and 150 ng/ml was investigated. The results showed that the sensitivity of the WcBiM sensor using the EDC-NHS-activated protein A, protein A, and SAM was 0.0185 [%/(ng/ml)], 0.0065 [%/(ng/ml)], and 0.0101 [%/(ng/ml)], respectively. The lowest detectable concentrations of IgG with the EDC-NHS-activated protein A, protein A, and SAM were 4.27, 12.83, and 8.24 ng/ml, respectively. Therefore, the increased sensitivity and lower detection capability of the WcBiM SPR chip with the EDC-NHS-activated protein A suggests that it could be used in early diagnosis where the trace level concentrations of biomolecules should be detected.

  4. CO2 Electroreduction on Well-Defined Bimetallic Surfaces

    DEFF Research Database (Denmark)

    Varela Gasque, Ana Sofia; Schlaup, Christian Georg; Jovanov, Zarko P.

    2013-01-01

    We have studied the electrochemical reduction of CO2 on Cu overlayers on Pt(111) and Pt(211) surfaces. These systems were chosen to investigate the effect of strain on the catalytic activity of Cu surfaces and to obtain information about the role of steps in this process. The selectivity toward h...

  5. Synthesis of supported bimetallic nanoparticles with controlled size and composition distributions for active site elucidation

    Energy Technology Data Exchange (ETDEWEB)

    Hakim, Sikander H.; Sener, Canan; Alba Rubio, Ana C.; Gostanian, Thomas M.; O' neill, Brandon J; Ribeiro, Fabio H.; Miller, Jeffrey T.; Dumesic, James A

    2015-08-01

    Elucidation of active sites in supported bimetallic catalysts is complicated by the high level of dispersity in the nanoparticle size and composition that is inherent in conventional methods of catalyst preparation. We present a synthesis strategy that leads to highly dispersed, bimetallic nanoparticles with uniform particle size and composition by means of controlled surface reactions. We demonstrate the synthesis of three systems, RhMo, PtMo, and RhRe, consisting of a highly reducible metal with an oxophilic promoter. These catalysts are characterized by FTIR, CO chemisorption, STEM/EDS, TPR, and XAS analysis. The catalytic properties of these bimetallic nanoparticles were probed for the selective CO hydrogenolysis of (hydroxymethyl)tetrahydropyran to produce 1,6 hexanediol. Based on the characterization results and reactivity trends, the active sites in the hydrogenolysis reaction are identified to be small ensembles of the more noble metal (Rh, Pt) adjacent to highly reduced moieties of the more oxophilic metal (Mo, Re).

  6. Effects of different additives on bimetallic Au-Pt nanoparticles electrodeposited onto indium tin oxide electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Ballarin, Barbara, E-mail: ballarin@ms.fci.unibo.i [Dipartimento di Chimica Fisica ed Inorganica, Universita di Bologna, V.le Risorgimento, 4, 40136-Bologna (Italy)] [INSTM, UdR Bologna (Italy); Gazzano, Massimo [ISOF-CNR, V. Selmi, 40126-Bologna (Italy); Tonelli, Domenica [Dipartimento di Chimica Fisica ed Inorganica, Universita di Bologna, V.le Risorgimento, 4, 40136-Bologna (Italy)] [INSTM, UdR Bologna (Italy)

    2010-09-01

    Bimetallic Au-Pt nanoparticles (Au-Pt{sub NPs}) have been synthesized using an electrochemical reduction approach. The effects of the addition of different additives in the electrodeposition bath namely KI, 1-nonanesulfonic acid sodium salt and Triton X-100 have been investigated. The structural characterization of the bimetallic nanoparticles has been carried out using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), UV-vis spectroscopy, X-ray diffraction (XRD) and cyclic voltammetry (CV). The Au-Pt{sub NPs} prepared in the presence of KI and Triton X-100 characterized by a relatively narrow size distribution as well as a higher particle density and surface coverage whereas no changes in the morphology were observed. These results suggest a dependence of the size and distribution of the bimetallic nanoparticles from the type and concentration of the additives employed.

  7. Silver-gold bimetallic nanoparticles and their applications as optical materials.

    Science.gov (United States)

    Boote, Brett W; Byun, Hongsik; Kim, Jun-Hyun

    2014-02-01

    Recently, nanoscale metallic particles have been studied extensively due to their tunable and strong optical properties that are well beyond those of organic chromophores. As monometallic nanoparticles have shown strong but narrow absorption bands within the ultraviolet and visible wavelengths, the preparation of bimetallic core-shell structures can give rise to strong, wide, and tunable absorption bands across the visible to near infrared areas. The silver-gold bimetallic nanoparticles with core-shell structures can offer unique physical and optical properties inaccessible to monometallic systems. These nanoparticles have been utilized in many areas of research including chemical catalysis, surface-enhanced Raman spectroscopy, and photothermal therapy. This review article is a comprehensive overview of bimetallic nanoparticle systems consisting of gold and silver; it is based on the recent advances in wet-chemical synthetic methodologies, the characterization of size and shape-dependent optical properties, and various optically driven applications including catalysis, signal-enhancing devices, and biomedical purposes.

  8. Dechlorination of disinfection by-product monochloroacetic acid in drinking water by nanoscale palladized iron bimetallic particle

    Institute of Scientific and Technical Information of China (English)

    CHEN Chao; WANG Xiangyu; CHANG Ying; LIU Huiling

    2008-01-01

    Nanoscale palladized iron (Pd/Fe) bimetallic particles were prepared by reductive deposition method. The particles were characterized by X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscope (SEM), transmission electron microscope (TEM), and Brunauer-Emmett-Teller-nitrogen (BET-N2) method. Data obtained from those methods indicated that nanoscale Pd/Fe bimetallic particles contained α-Fe0. Detected Pd to Fe ratio by weight (PFRW) was close to theoretical PFRW. Spherical granules with diameter of 47±11.5 nm connected with one another to form chains and the chains composed nanoscale Pd/Fe bimetallic particles. Specific surface area of particles was 51 m2/g. Factors, such as species of reductants, PFRW, dose of nanoscale Pd/Fe bimetallic particles added into solutions, solution initial pH, and a variety of solvents were studied. Dechlorination effect of monochloroacetic acid (MCAA) by different reductants followed the trend: nanoscale Pd/Fe bimetallic particles of 0.182% PFRW > nanoscale Fe > reductive Fe. When PFRW was lower than 0.083%, increasing PFRW would increase dechlorination efficiency (DE) of MCAA. But when the PFRW was higher than 0.083%, increasing PFRW caused decrease in DE. Adding more nanoscale Pd/Fe bimetallic particles to solution would enhance DE. The DE of MCAA decreased as initial pH of solution increased.

  9. Supported Pd-Cu bimetallic nanoparticles that have high activity for the electrochemical oxidation of methanol.

    Science.gov (United States)

    Yin, Zhen; Zhou, Wu; Gao, Yongjun; Ma, Ding; Kiely, Christopher J; Bao, Xinhe

    2012-04-16

    Monodisperse bimetallic Pd-Cu nanoparticles with controllable size and composition were synthesized by a one-step multiphase ethylene glycol (EG) method. Adjusting the stoichiometric ratio of the Pd and Cu precursors afforded nanoparticles with different compositions, such as Pd(85)-Cu(15), Pd(56)-Cu(44), and Pd(39)-Cu(61). The nanoparticles were separated from the solution mixture by extraction with non-polar solvents, such as n-hexane. Monodisperse bimetallic Pd-Cu nanoparticles with narrow size-distribution were obtained without the need for a size-selection process. Capping ligands that were bound to the surface of the particles were removed through heat treatment when the as-prepared nanoparticles were loaded onto a Vulcan XC-72 carbon support. Supported bimetallic Pd-Cu nanoparticles showed enhanced electrocatalytic activity towards methanol oxidation compared with supported Pd nanoparticles that were fabricated according to the same EG method. For a bimetallic Pd-Cu catalyst that contained 15 % Cu, the activity was even comparable to the state-of-the-art commercially available Pt/C catalysts. A STEM-HAADF study indicated that the formation of random solid-solution alloy structures in the bimetallic Pd(85)-Cu(15)/C catalysts played a key role in improving the electrochemical activity. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Synthesis of hollow Ag-Au bimetallic nanoparticles in polyelectrolyte multilayers.

    Science.gov (United States)

    Zhang, Xin; Zhang, Guangyu; Zhang, Bodong; Su, Zhaohui

    2013-06-04

    Ag nanoparticles of ~20 nm size and rather uniform size distribution were synthesized in polyelectrolyte multilayers (PEMs) via an ion-exchange/reduction process in two stages (seeding and growth), which were used as sacrificial templates to fabricate Ag-Au bimetallic hollow nanoparticles via galvanic replacement reaction. The reaction process was monitored by UV-vis spectroscopy. The morphology and structure of the nanoparticles were characterized by transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy, which confirmed the formation of hollow Ag-Au bimetallic nanoparticles. UV-vis absorbance spectroscopy and TEM results indicated that both size and optical properties of the Ag nanoparticles in the PEM can be controlled by manipulating ion content in the PEM and the number of the ion-exchange/reduction cycle, whereas that of Ag-Au bimetallic nanoparticles were dependent on size of the Ag templates and the replacement reaction kinetics. The hollow Ag-Au bimetallic nanoparticles exhibited a significant red shift in the surface plasmon resonance to the near-infrared region. The strategy enables facile preparation of hollow bimetallic nanoparticles in situ in polymer matrixes.

  11. Quantitative Prediction of Surface Segregation in Bimetallic Pt-MAlloy Nanoparticles (M=Ni, Re, Mo)

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Guofeng; Van Hove, Michel A.; Ross, Phil N.; Baskes,Michael I.

    2005-06-20

    This review addresses the issue of surface segregation inbimetallic alloy nanoparticles, which are relevant to heterogeneouscatalysis, in particular for electro-catalysts of fuel cells. We describeand discuss a theoretical approach to predicting surface segregation insuch nanoparticles by using the Modified Embedded Atom Method and MonteCarlo simulations. In this manner it is possible to systematicallyexplore the behavior of such nanoparticles as a function of componentmetals, composition, and particle size, among other variables. We choseto compare Pt75Ni25, Pt75Re25, and Pt80Mo20 alloys as example systems forthis discussion, due to the importance of Pt in catalytic processes andits high-cost. It is assumed that the equilibrium nanoparticles of thesealloys have a cubo-octahedral shape, the face-centered cubic lattice, andsizes ranging from 2.5 nm to 5.0 nm. By investigating the segregation ofPt atoms to the surfaces of the nanoparticles, we draw the followingconclusions from our simulations at T= 600 K. (1) Pt75Ni25 nanoparticlesform a surface-sandwich structure in which the Pt atoms are stronglyenriched in the outermost and third layers while the Ni atoms areenriched in the second layer. In particular, a nearly pure Pt outermostsurface layer can be achieved in those nanoparticles. (2) EquilibriumPt75Re25 nanoparticles adopt a core-shell structure: a nearly pure Ptshell surrounding a more uniform Pt-Re core. (3) In Pt80Mo20nanoparticles, the facets are fully occupied by Pt atoms, the Mo atomsonly appear at the edges and vertices, and the Pt and Mo atoms arrangethemselves in an alternating sequence along the edges and vertices. Oursimulations quantitatively agree with previous experimental andtheoretical results for the extended surfaces of Pt-Ni, Pt-Re, and Pt-Moalloys. We further discuss the reasons for the different types of surfacesegregation found in the different alloys, and some of theirimplications.

  12. The atomic structural dynamics of γ-Al2O3 supported Ir-Pt nanocluster catalysts prepared from a bimetallic molecular precursor: a study using aberration-corrected electron microscopy and X-ray absorption spectroscopy.

    Science.gov (United States)

    Small, Matthew W; Sanchez, Sergio I; Menard, Laurent D; Kang, Joo H; Frenkel, Anatoly I; Nuzzo, Ralph G

    2011-03-16

    This study describes a prototypical, bimetallic heterogeneous catalyst: compositionally well-defined Ir-Pt nanoclusters with sizes in the range of 1-2 nm supported on γ-Al(2)O(3). Deposition of the molecular bimetallic cluster [Ir(3)Pt(3)(μ-CO)(3)(CO)(3)(η-C(5)Me(5))(3)] on γ-Al(2)O(3), and its subsequent reduction with hydrogen, provides highly dispersed supported bimetallic Ir-Pt nanoparticles. Using spherical aberration-corrected scanning transmission electron microscopy (C(s)-STEM) and theoretical modeling of synchrotron-based X-ray absorption spectroscopy (XAS) measurements, our studies provide unambiguous structural assignments for this model catalytic system. The atomic resolution C(s)-STEM images reveal strong and specific lattice-directed strains in the clusters that follow local bonding configurations of the γ-Al(2)O(3) support. Combined nanobeam diffraction (NBD) and high-resolution transmission electron microscopy (HRTEM) data suggest the polycrystalline γ-Al(2)O(3) support material predominantly exposes (001) and (011) surface planes (ones commensurate with the zone axis orientations frequently exhibited by the bimetallic clusters). The data reveal that the supported bimetallic clusters exhibit complex patterns of structural dynamics, ones evidencing perturbations of an underlying oblate/hemispherical cuboctahedral cluster-core geometry with cores that are enriched in Ir (a result consistent with models based on surface energetics, which favor an ambient cluster termination by Pt) due to the dynamical responses of the M-M bonding to the specifics of the adsorbate and metal-support interactions. Taken together, the data demonstrate that strong temperature-dependent charge-transfer effects occur that are likely mediated variably by the cluster-support, cluster-adsorbate, and intermetallic bonding interactions.

  13. Ammonia Decomposition over Bimetallic Nitrides Supported on γ-Al2O3

    Institute of Scientific and Technical Information of China (English)

    Chun Shan LU; Xiao Nian LI; Yi Feng ZHU; Hua Zhang LIU; Chun Hui ZHOU

    2004-01-01

    A series of monometallic nitrides and bimetallic nitrides were prepared by temperature-programmed reaction with NH3. The effects of Co, Ni and Fe additives and the synergic action between Fe, Co, Ni and Mo on the ammonia decomposition activity were investigated. TPR-MS, XRD were also carried out to obtain better insight into the structure of the bimetallic nitride. The results of ammonia decomposition activity show that bimetallic nitrides are more active than monometallic nitrides or bimetallic oxides.

  14. Transmetallation as an effective strategy for the preparation of bimetallic CoPd and CuPd nanoparticles

    Science.gov (United States)

    Bersani, Marco; Conte, Luca; Martucci, Alessandro; Guglielmi, Massimo; Mattei, Giovanni; Bello, Valentina; Rosei, Renzo; Centazzo, Massimo

    2014-01-01

    The preparation of palladium alloy nanoparticles is of great interest for many applications, especially in catalysis. Starting from presynthesized nanoparticles of a less noble metal, a transmetallation reaction involving a redox process at the nanoparticle surface can be exploited to modify the nanoparticle composition and crystalline phase. As an example, monodispersed ε-cobalt and face-centered cubic copper nanoparticles were synthesized in organic solvents at high temperature and the as-formed nanoparticles were reacted with palladium(ii) hexafluoroacetylacetonate resulting in the formation of alloyed nanoparticles whose composition closely follows the reactant ratio. The oxidative state of the nanoparticle surface greatly affects the success of the transmetallation reaction and a reduction treatment was necessary to achieve the desired final product. Electron microscopy and X-ray diffraction showed that for cobalt a limiting palladium content for the ε-phase alloy is found, above which an fcc alloy nucleates, while for copper the fcc crystalline phase is preserved throughout the whole composition range.

  15. Preparation and characterization of agar-based nanocomposite films reinforced with bimetallic (Ag-Cu) alloy nanoparticles.

    Science.gov (United States)

    Arfat, Yasir Ali; Ahmed, Jasim; Jacob, Harsha

    2017-01-02

    Agar-based active nanocomposite films were prepared by incorporating silver-copper (Ag-Cu) alloy nanoparticles (NPs) (0.5-4wt%) into glycerol plasticized agar solution. Thermo-mechanical, morphological, structural, and optical properties of the nanocomposite films were characterized by texture analyzer, differential scanning calorimetry (DSC), scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier transforms infrared (FTIR) spectroscopy, and surface color measurement. Tensile strength and the melting temperature of the film increased linearly with NPs loading concentration. Color, transparency and UV barrier properties of agar films were influenced by the reinforcement of Ag-Cu NPs. XRD analysis confirmed the crystalline structure of the Agar/Ag-Cu nanocomposite films, whereas the smoothness and the homogeneity of film surface strongly reduced as observed through the SEM. The nanocomposite films exhibited a profound antibacterial activity against both Gram-positive (Listeria monocytogenes) and Gram-negative (Salmonella enterica sv typhimurium) bacteria. Overall, the agar nanocomposite films could be used as packaging material for food preservation by controlling foodborne pathogens and spoilage bacteria.

  16. Microbially supported synthesis of catalytically active bimetallic Pd-Au nanoparticles.

    Science.gov (United States)

    Hosseinkhani, Baharak; Søbjerg, Lina Sveidal; Rotaru, Amelia-Elena; Emtiazi, Giti; Skrydstrup, Troels; Meyer, Rikke Louise

    2012-01-01

    Bimetallic nanoparticles are considered the next generation of nanocatalysts with increased stability and catalytic activity. Bio-supported synthesis of monometallic nanoparticles has been proposed as an environmentally friendly alternative to the conventional chemical and physical protocols. In this study we synthesize bimetallic bio-supported Pd-Au nanoparticles for the first time using microorganisms as support material. The synthesis involved two steps: (1) Formation of monometallic bio-supported Pd(0) and Au(0) nanoparticles on the surface of Cupriavidus necator cells, and (2) formation of bimetallic bio-supported nanoparticles by reduction of either Au(III) or Pd(II) on to the nanoparticles prepared in step one. Bio-supported monometallic Pd(0) or Au(0) nanoparticles were formed on the surface of C. necator by reduction of Pd(II) or Au(III) with formate. Addition of Au(III) or Pd(II) to the bio-supported particles resulted in increased particle size. UV-Vis spectrophotometry and HR-TEM analyses indicated that the previously monometallic nanoparticles had become fully or partially covered by Au(0) or Pd(0), respectively. Furthermore, Energy Dispersive Spectrometry (EDS) and Fast Fourier Transformation (FFT) analyses confirmed that the nanoparticles indeed were bimetallic. The bimetallic nanoparticles did not have a core-shell structure, but were superior to monometallic particles at reducing p-nitrophenol to p-aminophenol. Hence, formation of microbially supported nanoparticles may be a cheap and environmentally friendly approach for production of bimetallic nanocatalysts. Copyright © 2011 Wiley Periodicals, Inc.

  17. Adsorption and dissociation of H{sub 2}S on monometallic and monolayer bimetallic Ni/Pd(111) surfaces: A first-principles study

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yi, E-mail: liy99@fzu.edu.cn [College of Chemistry, Fuzhou University, Fuzhou, Fujian, 350116 (China); Fujian Provincial Key Laboratory of Theoretical and Computational Chemistry, Xiamen, Fujian, 361005 (China); Huang, Pan; Tao, Dandan; Wu, Juan; Qiu, Mei; Huang, Xin; Ding, Kaining; Chen, Wenkai [College of Chemistry, Fuzhou University, Fuzhou, Fujian, 350116 (China); Su, Wenyue [State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou, Fujian, 350002 (China); Zhang, Yongfan, E-mail: zhangyf@fzu.edu.cn [College of Chemistry, Fuzhou University, Fuzhou, Fujian, 350116 (China); State Key Laboratory of Photocatalysis on Energy and Environment, Fuzhou, Fujian, 350002 (China)

    2016-11-30

    Highlights: • For the molecular adsorption, the introducing Ni monolayer on Pd(111) can reduce the binding strength between H{sub 2}S and the surface. • The decompositions of H{sub 2}S molecule on all Ni/Pd(111) surfaces are exothermic, especially for the surfaces that the top layer is composed of Ni atoms. • Monolayer Ni-Pd(111) surface may exhibit a good sulfur resistance performance because there is a competition between the desorption and decomposition of H{sub 2}S molecule. - Abstract: Periodic density functional theory calculations have been performed to investigate the adsorption structures and dissociative reaction pathways for H{sub 2}S molecule on Ni(111), Pd(111) and Ni/Pd(111) monolayer bimetallic surfaces with surface monolayer and subsurface monolayer structures. Our results indicate that, for the molecular adsorption mode, the introducing Pd atoms on Ni(111) can enhance the binding strength between H{sub 2}S and the surface, while an opposite effect is achieved when the Ni monolayer is formed on Pd(111) surface. The decompositions of H{sub 2}S molecule on all Ni/Pd(111) surfaces are exothermic, especially for the surfaces that the top layer is composed of Ni atoms. According to the predicted minimum energy paths that connect the molecular and dissociative states, two elementary steps are found for all Ni/Pd(111) metal surfaces, and the breaking of the first H−S bond is the rate-determining step for the H{sub 2}S dissociation. Our results reveal that in most cases, the decomposition of H{sub 2}S molecule on the monometallic and Ni/Pd(111) monolayer bimetallic surfaces is easy to happen. However, on the monolayer Ni-Pd(111) surface, there is a competition between the trapping-desorption channel and activated dissociation channel, which implies that depositing one monolayer Ni on a Pd(111) surface may help reducing sulfur poisoning by hindering the dissociation of H{sub 2}S molecule.

  18. Oxidation of CO and surface properties of well characterized Pt{sub 3}Sn bimetallic alloy surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Stamenkovic, V.; Arenz, M.; Blizanac, B. B.; Ross, P. N.; Markovic, N. M. [University of California-Berkeley, Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA (United States)

    2004-04-01

    The Pt{sub 3}Sn alloy is known to be one of the most active systems for carbon monoxide oxidation. This paper continues the effort begun earlier to explore the link between macroscopic level properties of the Pt{sub 3}Sn(hkl) surfaces in an electrochemical environment and in-situ atomic level characterization. Specifically, the work reported here entails a further examination of the Pt{sub 3}Sn(110) interface in an electrochemical environment as part of a detailed study of structural effects on electrocatalysis. Alloy surfaces have been characterized in ultra-high vacuum (UHV) by Auger electron microscopy, low energy ion scattering spectroscopy (LEISS) and low energy electron diffraction (LEED). Surface electrochemistry of carbon monoxide was studied in-situ by Fourier transform infrared (FTIR) spectroscopy. Result showed that in contrast to the Pt{sub 3}Sn(111) surface, changes in band morphology and vibrational properties are clearly absent on the Pt{sub 3}Sn(110) surface. In the case of the Pt{sub 3}Sn(hkl)-CO interaction, not only electronic effects, but also other factors, such as surface structure and intermolecular repulsion between adsorbed CO species were found to be responsible for high catalytic activity. 40 refs., 6 figs.

  19. Exceptional methanol electro-oxidation activity by bimetallic concave and dendritic Pt-Cu nanocrystals catalysts

    Science.gov (United States)

    Wang, Ying-Xia; Zhou, Hui-Jing; Sun, Ping-Chuan; Chen, Tie-Hong

    2014-01-01

    PtCux (x = 1, 2 and 3) bimetallic nanocrystals with concave surface and dendritic morphology were prepared and used as electrocatalysts in methanol oxidation reaction (MOR) for polymer electrolyte membrane fuel cells. The bimetallic nanocrystals were synthesized via one-pot co-reduction of H2PtCl6 and Cu(acac)2 by oleylamine and polyvinyl pyrrolidone (PVP) in an autoclave at 180 °C. The concave dendritic bimetallic nanostructure consisted of a core rich in Cu and nanodendrites rich in Pt, which was formed via galvanic replacement of Cu by Pt. It was found that PVP played an important role in initiating, facilitating, and directing the replacement reaction. The electrochemical properties of the PtCux were characterized by cyclic voltammetry (CV) and chronoamperometry (CA). The concave dendritic PtCu2/C nanocrystals exhibited exceptionally high activity and strong poisoning resistance in MOR. At 0.75 V (vs. reversible hydrogen electrode, RHE) the mass activity and specific activity of PtCu2/C were 3.3 and 4.1 times higher than those of the commercial Pt/C catalysts, respectively. The enhanced catalytic activity could be attributed to the unique concave dendritic morphology of the bimetallic nanocrystals.

  20. Platinum-ruthenium bimetallic clusters on graphite: a comparison of vapor deposition and electroless deposition methods.

    Science.gov (United States)

    Galhenage, Randima P; Xie, Kangmin; Diao, Weijian; Tengco, John Meynard M; Seuser, Grant S; Monnier, John R; Chen, Donna A

    2015-11-14

    Bimetallic Pt-Ru clusters have been grown on highly ordered pyrolytic graphite (HOPG) surfaces by vapor deposition and by electroless deposition. These studies help to bridge the material gap between well-characterized vapor deposited clusters and electrolessly deposited clusters, which are better suited for industrial catalyst preparation. In the vapor deposition experiments, bimetallic clusters were formed by the sequential deposition of Pt on Ru or Ru on Pt. Seed clusters of the first metal were grown on HOPG surfaces that were sputtered with Ar(+) to introduce defects, which act as nucleation sites for Pt or Ru. On the unmodified HOPG surface, both Pt and Ru clusters preferentially nucleated at the step edges, whereas on the sputtered surface, clusters with relatively uniform sizes and spatial distributions were formed. Low energy ion scattering experiments showed that the surface compositions of the bimetallic clusters are Pt-rich, regardless of the order of deposition, indicating that the interdiffusion of metals within the clusters is facile at room temperature. Bimetallic clusters on sputtered HOPG were prepared by the electroless deposition of Pt on Ru seed clusters from a Pt(+2) solution using dimethylamine borane as the reducing agent at pH 11 and 40 °C. After exposure to the electroless deposition bath, Pt was selectively deposited on Ru, as demonstrated by the detection of Pt on the surface by XPS, and the increase in the average cluster height without an increase in the number of clusters, indicating that Pt atoms are incorporated into the Ru seed clusters. Electroless deposition of Ru on Pt seed clusters was also achieved, but it should be noted that this deposition method is extremely sensitive to the presence of other metal ions in solution that have a higher reduction potential than the metal ion targeted for deposition.

  1. Carbon covered alumina prepared by the pyrolysis of sucrose: A promising support material for the supported Pt-Sn-bimetallic dehydrogenation catalysis

    NARCIS (Netherlands)

    Luo, S.; He, S.; Li, X.R.; Seshan, K.

    2014-01-01

    Sucrose was pyrolyzed on gamma alumina surface to prepare carbon covered alumina (CCA) material. Alumina and CCA supported Pt–Sn catalysts were prepared by the complex impregnation method under vacuum. Dehydrogenation of n-octadecane was performed to study the effect of carbon addition, Pt loading a

  2. Carbon covered alumina prepared by the pyrolysis of sucrose: A promising support material for the supported Pt-Sn-bimetallic dehydrogenation catalysis

    NARCIS (Netherlands)

    Luo, S.; He, Songbo; Li, X.R.; Seshan, Kulathuiyer

    2014-01-01

    Sucrose was pyrolyzed on gamma alumina surface to prepare carbon covered alumina (CCA) material. Alumina and CCA supported Pt–Sn catalysts were prepared by the complex impregnation method under vacuum. Dehydrogenation of n-octadecane was performed to study the effect of carbon addition, Pt loading

  3. Carbon covered alumina prepared by the pyrolysis of sucrose: A promising support material for the supported Pt-Sn-bimetallic dehydrogenation catalysis

    NARCIS (Netherlands)

    Luo, S.; He, Songbo; Li, X.R.; Seshan, Kulathuiyer

    2014-01-01

    Sucrose was pyrolyzed on gamma alumina surface to prepare carbon covered alumina (CCA) material. Alumina and CCA supported Pt–Sn catalysts were prepared by the complex impregnation method under vacuum. Dehydrogenation of n-octadecane was performed to study the effect of carbon addition, Pt loading a

  4. Synthesis of Anchored Bimetallic Catalysts via Epitaxy

    Directory of Open Access Journals (Sweden)

    Jiaxin Liu

    2016-06-01

    Full Text Available The development of thermodynamically stable supported bimetallic catalysts for high-temperature reaction is significant and highly desirable but remains a grand challenge. In this work, we report a novel approach that relies on the interaction of metal nanoparticles with the support material to form unique bimetallic nanoparticles, which epitaxially anchor onto the support surface. Such unique nanostructured systems are catalytically active and ultrastable during selected catalytic reactions. In this paper, we describe the synthesis processes of ultrastable PtZn nanoparticles epitaxially anchored onto ZnO nanowires, which primarily consist of {10−10} nanoscale facets. Such anchored PtZn nanoparticles demonstrated good stability during high temperature treatments and selected catalytic reactions. The synthesis approach reported in this work provides a new strategy to develop thermodynamically stable supported bimetallic catalysts.

  5. Magneto-optical response in bimetallic metamaterials

    CERN Document Server

    Atmatzakis, Evangelos; Fedotov, Vassili; Vienne, Guillaume; Zheludev, Nikolay I

    2016-01-01

    We demonstrate resonant Faraday polarization rotation in plasmonic arrays of bimetallic nano-ring resonators consisting of Au and Ni sections. This metamaterial design allows to optimize the trade-off between the enhancement of magneto-optical effects and plasmonic dissipation. Although Ni sections correspond to as little as ~6% of the total surface of the metamaterial, the resulting magneto-optically induced polarization rotation is equal to that of a continuous film. Such bimetallic metamaterials can be used in compact magnetic sensors, active plasmonic components and integrated photonic circuits.

  6. Preparation and Characterization of Bi-metallic and Tri-metallic Metal Organic Frameworks Based on Trimesic Acid and Co(II), Ni(II), and Cu(II) Ions

    Science.gov (United States)

    Sahiner, Nurettin; Demirci, Sahin; Yildiz, Mustafa

    2016-10-01

    Trimesic acid-M1(II):M2(II) (M1,2(II)=M(II)=Co(II), Ni(II) and Cu(II)) bi-metallic or tri-metallic organic frameworks (MOFs) were synthesized by the reaction of trimesic acid (H3BTC) ligand with the corresponding MCl2nH2O aqueous solutions. Here, bi- and tri-metallic MOF preparations were demonstrated by using H3BTC as an organic linker, with dual metal ion mixtures at different mole ratios such as Co(II):Ni(II), Ni(II):Cu(II), and Cu(II):Co(II) as metal ion sources in the synthesis of bi-metallic MOFs, and the triple metal ion mixture of Co(II):Ni(II):Cu(II) as the metal ion source in the synthesis of tri-metallic MOFs. The bi- or tri-metallic MOFs were characterized via the Brunauer-Emmett-Teller method, thermogravimetric analyzer (TGA), and magnetic susceptibility measurements with the Gouy method, FT-IR spectroscopy, and electronic spectral studies. The results revealed that the H3BTC MOFs have octahedral and distorted octahedral arrangement around the metal ions, and the d-d transition was not observed in the complex. It was further found that all the prepared MOFs contain water molecules confirmed by Fourier transform infrared (FT-IR) and TGA analyses. The FT-IR spectra of the MOF complexes were characterized by the appearance of a broad band in the region of 3454-3300 cm-1 due to the ν(-OH) of the coordinated water; therefore, the location of the two water molecules was assumed to be inside the complex structure. Remarkably, the synthesized bi-metallic MOFs had unique and distinct colors depending on the amounts of metal ions used in the feed, implying that these bi-metallic MOFs with tunable M1(II) and M2(II) ratios offer great potential in the design of color-coded materials for use as sensors.

  7. Preparation and Characterization of Bi-metallic and Tri-metallic Metal Organic Frameworks Based on Trimesic Acid and Co(II), Ni(II), and Cu(II) Ions

    Science.gov (United States)

    Sahiner, Nurettin; Demirci, Sahin; Yildiz, Mustafa

    2017-02-01

    Trimesic acid-M1(II):M2(II) (M1,2(II)=M(II)=Co(II), Ni(II) and Cu(II)) bi-metallic or tri-metallic organic frameworks (MOFs) were synthesized by the reaction of trimesic acid (H3BTC) ligand with the corresponding MCl2nH2O aqueous solutions. Here, bi- and tri-metallic MOF preparations were demonstrated by using H3BTC as an organic linker, with dual metal ion mixtures at different mole ratios such as Co(II):Ni(II), Ni(II):Cu(II), and Cu(II):Co(II) as metal ion sources in the synthesis of bi-metallic MOFs, and the triple metal ion mixture of Co(II):Ni(II):Cu(II) as the metal ion source in the synthesis of tri-metallic MOFs. The bi- or tri-metallic MOFs were characterized via the Brunauer-Emmett-Teller method, thermogravimetric analyzer (TGA), and magnetic susceptibility measurements with the Gouy method, FT-IR spectroscopy, and electronic spectral studies. The results revealed that the H3BTC MOFs have octahedral and distorted octahedral arrangement around the metal ions, and the d-d transition was not observed in the complex. It was further found that all the prepared MOFs contain water molecules confirmed by Fourier transform infrared (FT-IR) and TGA analyses. The FT-IR spectra of the MOF complexes were characterized by the appearance of a broad band in the region of 3454-3300 cm-1 due to the ν(-OH) of the coordinated water; therefore, the location of the two water molecules was assumed to be inside the complex structure. Remarkably, the synthesized bi-metallic MOFs had unique and distinct colors depending on the amounts of metal ions used in the feed, implying that these bi-metallic MOFs with tunable M1(II) and M2(II) ratios offer great potential in the design of color-coded materials for use as sensors.

  8. Biosensors Incorporating Bimetallic Nanoparticles

    Directory of Open Access Journals (Sweden)

    John Rick

    2015-12-01

    Full Text Available This article presents a review of electrochemical bio-sensing for target analytes based on the use of electrocatalytic bimetallic nanoparticles (NPs, which can improve both the sensitivity and selectivity of biosensors. The review moves quickly from an introduction to the field of bio-sensing, to the importance of biosensors in today’s society, the nature of the electrochemical methods employed and the attendant problems encountered. The role of electrocatalysts is introduced with reference to the three generations of biosensors. The contributions made by previous workers using bimetallic constructs, grouped by target analyte, are then examined in detail; following which, the synthesis and characterization of the catalytic particles is examined prior to a summary of the current state of endeavor. Finally, some perspectives for the future of bimetallic NPs in biosensors are given.

  9. Biosensors Incorporating Bimetallic Nanoparticles.

    Science.gov (United States)

    Rick, John; Tsai, Meng-Che; Hwang, Bing Joe

    2015-12-31

    This article presents a review of electrochemical bio-sensing for target analytes based on the use of electrocatalytic bimetallic nanoparticles (NPs), which can improve both the sensitivity and selectivity of biosensors. The review moves quickly from an introduction to the field of bio-sensing, to the importance of biosensors in today's society, the nature of the electrochemical methods employed and the attendant problems encountered. The role of electrocatalysts is introduced with reference to the three generations of biosensors. The contributions made by previous workers using bimetallic constructs, grouped by target analyte, are then examined in detail; following which, the synthesis and characterization of the catalytic particles is examined prior to a summary of the current state of endeavor. Finally, some perspectives for the future of bimetallic NPs in biosensors are given.

  10. Preparation of Cobalt-Molybdenum bimetallic oxides supported on alumina by Co-precipitation method%氧化铝负载Co-Mo双金属氧化物的共沉淀制备

    Institute of Scientific and Technical Information of China (English)

    张新波; 张斌; 张雅娟; 秦永华

    2012-01-01

    采用双溶剂体系(硝酸铝和硝酸钴的乙醇溶液与钼酸铵的碳酸铵水溶液)共沉淀制备了氧化铝负载Co-Mo双金属氧化物.研究了双溶剂体系中乙醇和水的体积比对共沉淀的影响,考察了老化时间对氧化物结构参数的影响,研究了焙烧温度对氧化物还原性能的影响.结果表明:乙醇和水体积比对钼酸根离子的沉淀有重要影响,为了保证钼酸根离子的完全沉淀,乙醇的体积要随着MoO3负载量的增加而提高;随着老化时间的增加,氧化物的比表面积先增加后下降,6h 老化的样品具有最大的比表面积;低温焙烧制得的氧化物较容易还原.%Cobalt-molybdenum bimetallic oxides supported on alumina were prepared by co-precipitation method with etha- nol-water binary solvent system,which is composed of ethanol solution of aluminium nitrate and cobalt nitrate, and aqueous solution of ammonium carbonate and ammonium molybdate. The effects of ethanol/water volume ratio and MoO3 loading ore the coprecipitation were invesitigated. X-ray diffraction ( XRD) , N2 physical adsorption and temperature programmed reduction (TPR) were employed to characterize the oxides. Results show that the precipitation of Mo7O246- ions was affected by the ethanol/water volume ratio and MoO3 loading. The volume of ethanol to guarantee the precipitation of Mo7O246~ ions should be increased with the increase of MoO, loading. The specific surface area firstly increased then decreased with the increase of aging time. The oxide with aging time of 6 h has the largest specific surface area. The oxides calcined at low temperature are reduced more easily than that calcined at high temperature.

  11. Preparation of stable silica surfaces for surface forces measurement

    Science.gov (United States)

    Ren, Huai-Yin; Mizukami, Masashi; Kurihara, Kazue

    2017-09-01

    A surface forces apparatus (SFA) measures the forces between two surfaces as a function of the surface separation distance. It is regarded as an essential tool for studying the interactions between two surfaces. However, sample surfaces used for the conventional SFA measurements have been mostly limited to thin (ca. 2-3 μm) micas, which are coated with silver layers (ca. 50 nm) on their back, due to the requirement of the distance determination by transmission mode optical interferometry called FECO (fringes of equal chromatic order). The FECO method has the advantage of determining the absolute distance, so it should be important to increase the availability of samples other than mica, which is chemically nonreactive and also requires significant efforts for cleaving. Recently, silica sheets have been occasionally used in place of mica, which increases the possibility of surface modification. However, in this case, the silver layer side of the sheet is glued on a cylindrical quartz disc using epoxy resin, which is not stable in organic solvents and can be easily swollen or dissolved. The preparation of substrates more stable under severe conditions, such as in organic solvents, is necessary for extending application of the measurement. In this study, we report an easy method for preparing stable silica layers of ca. 2 μm in thickness deposited on gold layers (41 nm)/silica discs by sputtering, then annealed to enhance the stability. The obtained silica layers were stable and showed no swelling in organic solvents such as ethanol and toluene.

  12. Preparation of Pd/Pt Bimetallic Electrodes and Its Activity Toward Oxygen Reduction Reaction%Pd/Pt二元合金电极的制备及氧还原性能

    Institute of Scientific and Technical Information of China (English)

    方兰兰; 廖玲文; 刘少雄; 蔡俊; 李明芳; 陈艳霞

    2011-01-01

    利用Pt置换取代经欠电位沉积的亚单层Cu的方法,制备了不同组成的Pd/Pt二元合金电极(用Pd/Pt表示,x表示n置换取代欠电位沉积Cu过程的次数),并对其表面元素组成和氧还原性能进行了表征.在控制欠电位沉积Cu的下限电位恒定(0.34 V)的条件下,表面Pd/Pt的元素组成比通过重复Pt置换取代欠电位沉积Cu的次数(1~5次)来调控.光电子能谱(XPS)以及红外光谱实验结果表明,Pd/Pt电极表面的Pd/Pt元素组成比随着Pt沉积次数的增加而增加,对Pd/Pt电极,在电极表层约2~3 nm厚度内的Pt/Pd原子比为1:4,最表层的Pt/Pd原子比为4:1.循环伏安结果显示,随着Pt沉积次数的增加(1~5次),Pd/Pt电极表面越来越不易氧化.氧还原测试结果显示,随着Pt沉积次数(1~4次)的增加,Pd/Pt二元金属电极的氧还原活性依次增加,经过第3次沉积后其氧还原活性已优于纯Pt,而经4次以上沉积后其氧还原活性基本不变.在其它反应条件相同时,Pd/Pt电极上氧还原的半波电位与纯Pt相比右移约25 mV.可初步认为Pd/Pt二元金属体系氧还原性能的改善主要源自表层Pd原子让邻近的Pt原子上含氧物种的吸附能降低.%Pd/Pt bimetallic electrodes were prepared using under-potential deposition(UPD) of Cu following with galvanic displacement of Cu by Pt. The atomic ratios of Pt/Pd in the surface region can be tuned by holding the Cu UPD potential and changing the cycled times of UPD Cu and Pt-Cu displacement processes.Measurements using X-ray photon-electron spectroscopy(XPS) and electrochemical infrared spectroscopy( EC-IRS) with CO as probe molecules demonstrate that the atomic ratios of Pt/Pd increase monotonically with the cycle times of Cu-upd and Pt-Cu displacement. For Pd/Pt4 electrode, the average atomic ratios of Pt/Pd within 2—3 nm from the surface and at the surface are ca. 1: 4 and 4: 1, respectively. With the increase of Pt molar ratio at the surface, Pd

  13. Modeling the melting temperature of nanoscaled bimetallic alloys.

    Science.gov (United States)

    Li, Ming; Zhu, Tian-Shu

    2016-06-22

    The effect of size, composition and dimension on the melting temperature of nanoscaled bimetallic alloys was investigated by considering the interatomic interaction. The established thermodynamics model without any arbitrarily adjustable parameters can be used to predict the melting temperature of nanoscaled bimetallic alloys. It is found that, the melting temperature and interatomic interaction of nanoscaled bimetallic alloys decrease with the decrease in size and the increasing composition of the lower surface energy metal. Moreover, for the nanoscaled bimetallic alloys with the same size and composition, the dependence of the melting temperature on the dimension can be sequenced as follows: nanoparticles > nanowires > thin films. The accuracy of the developed model is verified by the recent experimental and computer simulation results.

  14. Levulinic acid hydrogenolysis on Al2O3-based Ni-Cu bimetallic catalysts

    Institute of Scientific and Technical Information of China (English)

    Iker Obregón; Eriz Corro; Urko Izquierdo; Jesus Requies; Pedro L. Arias

    2014-01-01

    Inexpensive γ-alumina-based nickel-copper bimetallic catalysts were studied for the hydrogenolysis of levulinic acid, a key platform molecule for biomass conversion to biofuels and other valued chemicals, into γ-valerolactone as a first step towards the production of 2-methyltetrahydrofurane. The activities of both monometallic and bimetallic catalysts were tested. Their textural and chemical characteristics were determined by nitrogen physisorption, elemental analysis, temperature-pro-grammed ammonia desorption, and temperature-programmed reduction. The monometallic nickel catalyst showed high activity but the highest by-product production and significant amounts of carbon deposited on the catalyst surface. The copper monometallic catalyst showed the lowest activity but the lowest carbon deposition. The incorporation of the two metals generated a bimetal-lic catalyst that displayed a similar activity to that of the Ni monometallic catalyst and significantly low by-product and carbon contents, indicating the occurrence of important synergetic effects. The influence of the preparation method was also examined by studying impregnated- and sol-gel-derived bimetallic catalysts. A strong dependency on the preparation procedure and calcina-tion temperature was observed. The highest activity per metal atom was achieved using the sol-gel-derived catalyst that was calcined at 450 °C. High reaction rates were achieved;the total levulinic acid conversion was obtained in less than 2 h of reaction time, yielding up to 96%γ-valerolactone, at operating temperature and pressure of 250 °C and 6.5 MPa hydrogen, respec-tively.

  15. Core/shell formation and surface segregation of multi shell icosahedral silver-palladium bimetallic nanostructures: A dynamic and thermodynamic study

    Energy Technology Data Exchange (ETDEWEB)

    Hewage, Jinasena W., E-mail: jinasena@chem.ruh.ac.lk

    2016-05-01

    Core/shell formation and surface segregation of multi shell icosahedral bimetallic silver-palladium nanostructures with the size of 55 and 147 atoms were studied by using the Molecular Dynamics simulations, and calculating Helmholtz free energy changes in the penetration of palladium atoms from shell to core, core to shell transition of silver and melting temperatures by using statistical mechanical densities of states. In 55 atoms icosahedra, two core–shell motifs, Ag{sub 13}Pd{sub 42} and Pd{sub 13}Ag{sub 42} with their isomers Pd{sub 13}(Pd{sub 29}Ag{sub 13}) and Ag{sub 13}(Ag{sub 29}Pd{sub 13}) were considered. Similarly in 147 atoms icosahedra, all mutations corresponding to the occupations of either silver atoms or palladium atoms in the core, inner shell or outer shell and their isomers generated by interchanging thirteen core atoms with thirteen atoms of the other type in the inner and outer shells were considered. It is found that the palladium-core clusters are more stable than the silver-core clusters and cohesive energy increases with the palladium composition. Phase transition of each cluster was studied by means of constant volume heat capacity. The trend in variation of melting temperature is accordance with the energy trend. Helmholtz free energy changes in palladium penetration, core to shell transition of silver and in surface mixing and segregation revealed the thermodynamic stability of the formation of Pd{sub core}Ag{sub shell} structures especially at silver rich environment and the surface segregation of silver. - Highlights: • Nanostructures of Pd{sub m}Ag{sub n} clusters for m + n = 55 and 147 have been studied. • Structures favor the formation of palladium-core surrounded by silver shell. • Calculated thermodynamic parameters confirm the energetic results. • Core/shell formation is favored at concentration of silver. • Silver segregation on surface while palladium penetration to core is observed.

  16. Segregation and phase dynamics in supported bimetallic nanoparticles

    Science.gov (United States)

    Nashner, Michael Sydney

    1997-12-01

    A set of supported bimetallic catalysts, designated lbrack Resb7Ir-Nrbrack,\\ lbrack Resb7Ir-Prbrack,\\ lbrack Resb5IrResb2-Prbrack, and lbrack Resb5IrResb2-Prbrack, has been prepared from two structural isomers of the cluster compound (Z) sb2lbrack Resb7IrC(CO)sb{23}rbrack\\ (Zsp+=NEtsb4sp+,\\ N(PPhsb3)sb2sp+) by deposition onto high surface area alumina ({≤}1% Re) and activation in Hsb2 at 773 K. The more active catalysts (lbrack Resb7Ir-N) and lbrack Resb5IrResb2-Nrbrack) are modeled by a hemisphere of close-packed (hcp) metal atoms (avg. diameter 1 nm) with Ir at the core. On the other hand the less active catalysts (lbrack Resb7Ir-Prbrack and lbrack Resb5IrResb2-Prbrack) are better described as two-dimensional layer structures. Supported bimetallic particles were obtained by reduction of the neutral molecular carbonyl cluster precursor PtRusb5C(CO)sb{16} with hydrogen. A detailed structural model of the nanoparticles has been deduced on the basis of studies by in-situ extended x-ray absorption fine structure spectroscopy (EXAFS), scanning transmission electron microscopy (STEM), microprobe energy dispersive x-ray (EDX) analysis, and electron microdiffraction. These experiments show that the bimetallic nanoparticles have a Pt:Ru composition of 1:5, an average diameter of ca. 1.5 nm, and adopt a face-centered cubic (fcc) closest packing structure. The local metal coordination environment, revealed by multiple scattering analysis of the EXAFS data, shows Pt segregation to the particle surfaces under an ambient Hsb2 atmosphere. The incipient lbrack PtRusb5rbrack nanoparticles were found to nucleate from a disordered structure where Pt is found in highly coordinating environments (i.e., the core) at temperatures as low as 473 K. This structure inverts to form the structure with surface segregated Pt. The reaction between a silicon monolayer deposited on Pt(111) by chemical vapor deposition (CVD) using silane (SiHsb4) is described. Using Auger electron

  17. Bimetallic ruthenium-copper nanoparticles embedded in mesoporous carbon as an effective hydrogenation catalyst.

    Science.gov (United States)

    Liu, Jiajia; Zhang, Li Li; Zhang, Jiatao; Liu, Tao; Zhao, X S

    2013-11-21

    Bimetallic ruthenium-copper nanoparticles embedded in the pore walls of mesoporous carbon were prepared via a template route and evaluated in terms of catalytic properties in D-glucose hydrogenation. The existence of bimetallic entities was supported by Ru L3-edge and Cu K-edge X-ray absorption results. The hydrogen spillover effect of the bimetallic catalyst on the hydrogenation reaction was evidenced by the results of both hydrogen and carbon monoxide chemisorptions. The bimetallic catalyst displayed a higher catalytic activity than the single-metal catalysts prepared using the same approach, namely ruthenium or copper nanoparticles embedded in the pore walls of mesoporous carbon. This improvement was due to the changes in the geometric and electronic structures of the bimetallic catalyst because of the presence of the second metal.

  18. Lignin-derived oxygenate reforming on a bimetallic surface: The reaction of benzaldehyde on Zn/Pt(111)

    Science.gov (United States)

    Shi, Daming; Vohs, John M.

    2016-08-01

    Temperature programmed desorption (TPD) and high-resolution electron energy loss spectroscopy (HREELS) were used to characterize the adsorption and reaction of benzaldehyde (C6H5CHO) on hydrogen-covered Pt(111) and Zn-modified Pt(111) surfaces. Benzaldehyde was found to interact with Pt(111) via both the phenyl ring and carbonyl of the aldehyde group. This bonding configuration facilitates unselective decomposition of the benzaldehyde to produce CO, H2, and small hydrocarbon fragments at relatively low temperatures. On the other hand, benzaldehyde was found to bond to Zn-decorated Pt(111) surface exclusively via the carbonyl group in an η2(C, O) configuration, with the phenyl ring tilted away from the surface. This configuration weakens Csbnd O bond in the carbonyl facilitating its cleavage and helps prevent hydrogenation of the phenyl ring.

  19. Electrodeposition of Au/Ag bimetallic dendrites assisted by Faradaic AC-electroosmosis flow

    Energy Technology Data Exchange (ETDEWEB)

    Ji, Jianlong; Li, Pengwei; Sang, Shengbo, E-mail: sbsang@tyut.edu.cn; Zhang, Wendong, E-mail: wdzhang@tyut.edu.cn; Li, Gang; Hu, Jie [Micro and Nano-system Research Centre, College of Information Engineering, Taiyuan University of Technology, 030024, Taiyuan (China); Zhou, Zhaoying, E-mail: zhouzy@mail.tsinghua.edu.cn; Yang, Xing; Dong, Hualai [MEMS Laboratory, Department of Precision Instruments, Tsinghua University, 100084, Beijing (China)

    2014-03-15

    Au/Ag bimetallic dendrites were synthesized successfully from the corresponding aqueous solution via the AC electrodeposition method. Both of the morphologies and compositions could be tuned by the electrolyte concentration and AC frequency. The prepared bimetallic dendrites were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectrometer (EDS), transmission electron microscopy (TEM) and UV–vis spectroscopy. The underlying dendrite growth mechanism was then proposed in the context of the Directed Electrochemical Nanowires Assembly (DENA) models. Owing to the unscreened voltage dropping in the electrolyte bulk, electromigration dominates the species flux process, and cations tend to accumulate in areas with strong electric field intensity, such as electrode edges. Moreover, Faradaic AC-electro-osmosis (ACEO) flow could increase the effective diffusion layer thickness in these areas during the electrochemical reaction, and leads to dendrite growth. Further Micro-Raman observations illustrated that the Au/Ag bimetallic dendrites exhibited pronounced surface-enhanced Raman scattering (SERS) activity, using 4-mercaptopyridine (4-MP) as model molecules.

  20. Electrodeposition of Au/Ag bimetallic dendrites assisted by Faradaic AC-electroosmosis flow

    Science.gov (United States)

    Ji, Jianlong; Li, Pengwei; Sang, Shengbo; Zhang, Wendong; Zhou, Zhaoying; Yang, Xing; Dong, Hualai; Li, Gang; Hu, Jie

    2014-03-01

    Au/Ag bimetallic dendrites were synthesized successfully from the corresponding aqueous solution via the AC electrodeposition method. Both of the morphologies and compositions could be tuned by the electrolyte concentration and AC frequency. The prepared bimetallic dendrites were characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectrometer (EDS), transmission electron microscopy (TEM) and UV-vis spectroscopy. The underlying dendrite growth mechanism was then proposed in the context of the Directed Electrochemical Nanowires Assembly (DENA) models. Owing to the unscreened voltage dropping in the electrolyte bulk, electromigration dominates the species flux process, and cations tend to accumulate in areas with strong electric field intensity, such as electrode edges. Moreover, Faradaic AC-electro-osmosis (ACEO) flow could increase the effective diffusion layer thickness in these areas during the electrochemical reaction, and leads to dendrite growth. Further Micro-Raman observations illustrated that the Au/Ag bimetallic dendrites exhibited pronounced surface-enhanced Raman scattering (SERS) activity, using 4-mercaptopyridine (4-MP) as model molecules.

  1. Air stable magnetic bimetallic Fe-Ag nanoparticles for advanced antimicrobial treatment and phosphorus removal.

    Science.gov (United States)

    Marková, Zdenka; Šišková, Karolína Machalová; Filip, Jan; Čuda, Jan; Kolář, Milan; Šafářová, Klára; Medřík, Ivo; Zbořil, Radek

    2013-05-21

    We report on new magnetic bimetallic Fe-Ag nanoparticles (NPs) which exhibit significant antibacterial and antifungal activities against a variety of microorganisms including disease causing pathogens, as well as prolonged action and high efficiency of phosphorus removal. The preparation of these multifunctional hybrids, based on direct reduction of silver ions by commercially available zerovalent iron nanoparticles (nZVI) is fast, simple, feasible in a large scale with a controllable silver NP content and size. The microscopic observations (transmission electron microscopy, scanning electron microscopy/electron diffraction spectroscopy) and phase analyses (X-ray diffraction, Mössbauer spectroscopy) reveal the formation of Fe₃O₄/γ-FeOOH double shell on a "redox" active nZVI surface. This shell is probably responsible for high stability of magnetic bimetallic Fe-Ag NPs during storage in air. Silver NPs, ranging between 10 and 30 nm depending on the initial concentration of AgNO₃, are firmly bound to Fe NPs, which prevents their release even during a long-term sonication. Taking into account the possibility of easy magnetic separation of the novel bimetallic Fe-Ag NPs, they represent a highly promising material for advanced antimicrobial and reductive water treatment technologies.

  2. Electrodeposition of Au/Ag bimetallic dendrites assisted by Faradaic AC-electroosmosis flow

    Directory of Open Access Journals (Sweden)

    Jianlong Ji

    2014-03-01

    Full Text Available Au/Ag bimetallic dendrites were synthesized successfully from the corresponding aqueous solution via the AC electrodeposition method. Both of the morphologies and compositions could be tuned by the electrolyte concentration and AC frequency. The prepared bimetallic dendrites were characterized by scanning electron microscopy (SEM, energy dispersive X-ray spectrometer (EDS, transmission electron microscopy (TEM and UV–vis spectroscopy. The underlying dendrite growth mechanism was then proposed in the context of the Directed Electrochemical Nanowires Assembly (DENA models. Owing to the unscreened voltage dropping in the electrolyte bulk, electromigration dominates the species flux process, and cations tend to accumulate in areas with strong electric field intensity, such as electrode edges. Moreover, Faradaic AC-electro-osmosis (ACEO flow could increase the effective diffusion layer thickness in these areas during the electrochemical reaction, and leads to dendrite growth. Further Micro-Raman observations illustrated that the Au/Ag bimetallic dendrites exhibited pronounced surface-enhanced Raman scattering (SERS activity, using 4-mercaptopyridine (4-MP as model molecules.

  3. Role of strain and ligand effects in the modification of the electronic and chemical properties of bimetallic surfaces

    DEFF Research Database (Denmark)

    Kitchin, J.R.; Nørskov, Jens Kehlet; Barteau, M.A.;

    2004-01-01

    Periodic density functional calculations are used to illustrate how the combination of strain and ligand effects modify the electronic and surface chemical properties of Ni, Pd, and Pt monolayers supported on other transition metals. Strain and the ligand effects are shown to change the width...

  4. Bimetallic layered castings alloy steel – carbon cast steel

    Directory of Open Access Journals (Sweden)

    T. Wróbel

    2011-01-01

    Full Text Available In paper is presented technology of bimetallic layered castings based on founding method of layer coating directly in cast processso-called method of mould cavity preparation. Prepared castings consist two fundamental parts i.e. bearing part and working part (layer. The bearing part of bimetallic layered casting is typical foundry material i.e. ferritic-pearlitic carbon cast steel, whereas working part (layer is plate of austenitic alloy steel sort X10CrNi 18-8. The ratio of thickness between bearing and working part is 8:1. The quality of the bimetallic layered castings was evaluated on the basis of ultrasonic NDT (non-destructive testing, structure and macro- and microhardness researches.

  5. Examples of material solutions in bimetallic layered castings

    Directory of Open Access Journals (Sweden)

    S. Tenerowicz

    2011-07-01

    Full Text Available In paper is presented technology of bimetallic layered castings based on founding method of layer coating directly in cast process so-called method of mould cavity preparation. Prepared castings consist two fundamental parts i.e. bearing part and working part (layer. The bearing part of bimetallic layered casting is typical foundry material i.e. pearlitic grey cast iron, whereas working part (layer is depending on accepted variant plates of alloy steels sort X6Cr13, X12Cr13, X10CrNi18-8 and X2CrNiMoN22-5-3. The ratio of thickness between bearing and working part is 8:1. The verification of the bimetallic layered castings was evaluated on the basis of ultrasonic NDT (non-destructive testing, structure and macro- and microhardness researches.

  6. Sonophotodeposition of bimetallic photocatalysts Pd-Au/TiO2 : application to selective oxidation of methanol to methyl formate.

    Science.gov (United States)

    Colmenares, Juan C; Lisowski, Paweł; Łomot, Dariusz; Chernyayeva, Olga; Lisovytskiy, Dmytro

    2015-05-22

    The aim of this work is to develop bimetallic Pd-Au/TiO2 P90 systems, which are highly active and selective for the photocatalytic oxidation of methanol to form methyl formate. Modification of commercial TiO2 P90 with Pd-Au nanoparticles was successfully achieved for the first time by means of a sonophotodeposition (SPD) method. The prepared materials were characterized by TEM, UV/Vis spectroscopy, X-ray photoelectron spectroscopy, and powder XRD. The Pd-Au bimetallic nanoparticles supported on titania exhibited remarkably enhanced catalytic activity in selective methanol oxidation to form methyl formate due to the synergism of Au and Pd particles, as well as the strong interaction between TiO2 and Pd-Au. SPD is a green methodology that can be used to prepare well-defined bimetallic surfaces on semiconductor supports with great promise for catalytic applications, in which selectivity can be tuned through adjustment of the surface composition.

  7. Bimetallic nanoalloys in heterogeneous catalysis of industrially important reactions: synergistic effects and structural organization of active components

    Science.gov (United States)

    Ellert, O. G.; Tsodikov, M. V.; Nikolaev, S. A.; Novotortsev, V. M.

    2014-08-01

    The review is concerned with correlations between the synergistic effects and structural organization of the surface of bimetallic alloys that are used as active components of catalysts for selective hydrogenation of organic compounds and for CO oxidation in hydrogen-rich mixtures. Studies on the preparation of novel highly efficient catalysts using modern theoretical approaches, computer-assisted molecular design and original synthetic procedures are considered. It is shown that introduction of the second metal into the monometallic catalyst and subsequent formation of alloy particles with modified structure of the surface and near-surface layers leads to nonadditive enhancement of catalytic activity and/or selectivity. The bibliography includes 203 references.

  8. Structure-Property Relationship in Metal Carbides and Bimetallic Alloys

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jingguan [University of Delaware

    2014-03-04

    The primary objective of our DOE/BES sponsored research is to use carbide and bimetallic catalysts as model systems to demonstrate the feasibility of tuning the catalytic activity, selectivity and stability. Our efforts involve three parallel approaches, with the aim at studying single crystal model surfaces and bridging the “materials gap” and “pressure gap” between fundamental surface science studies and real world catalysis. The utilization of the three parallel approaches has led to the discovery of many intriguing catalytic properties of carbide and bimetallic surfaces and catalysts. During the past funding period we have utilized these combined research approaches to explore the possibility of predicting and verifying bimetallic and carbide combinations with enhanced catalytic activity, selectivity and stability.

  9. Sample preparation for SEM of plant surfaces

    Directory of Open Access Journals (Sweden)

    A.K. Pathan

    2010-01-01

    Full Text Available Plant tissues must be dehydrated for observation in most electron microscopes. Although a number of sample processing techniques have been developed for preserving plant tissues in their original form and structure, none of them are guaranteed artefact-free. The current paper reviews common scanning electron microscopy techniques and the sample preparation methods employed for visualisation of leaves under specific types of electron microscopes. Common artefacts introduced by specific techniques on different leaf types are discussed. Comparative examples are depicted from our lab using similar techniques; the pros and cons for specific techniques are discussed. New promising techniques and microscopes, which can alleviate some of the problems encountered in conventional methods of leaf sample processing and visualisation, are also discussed. It is concluded that the choice of technique for a specific leaf sample is dictated by the surface features that need to be preserved (such as trichomes, epidermal cells or wax microstructure, the resolution to be achieved, availability of the appropriate processing equipment and the technical capabilities of the available electron microscope.

  10. XPS/STM study of model bimetallic Pd–Au/HOPG catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Bukhtiyarov, Andrey V., E-mail: avb@catalysis.ru [Boreskov Institute of Catalysis, Lavrentieva Ave. 5, 630090 Novosibirsk (Russian Federation); Novosibirsk State University, Pirogova str. 2, 630090 Novosibirsk (Russian Federation); Prosvirin, Igor P., E-mail: prosvirin@catalysis.ru [Boreskov Institute of Catalysis, Lavrentieva Ave. 5, 630090 Novosibirsk (Russian Federation); Novosibirsk State University, Pirogova str. 2, 630090 Novosibirsk (Russian Federation); Bukhtiyarov, Valerii I., E-mail: vib@catalysis.ru [Boreskov Institute of Catalysis, Lavrentieva Ave. 5, 630090 Novosibirsk (Russian Federation); Novosibirsk State University, Pirogova str. 2, 630090 Novosibirsk (Russian Federation)

    2016-03-30

    Graphical abstract: - Highlights: • The model Pd–Au/HOPG catalysts preparation has been studied by XPS and STM. • Model “core–shell” type Pd–Au/HOPG catalysts with different Pd/Au ratios were prepared. • Heating of the “core–shell” Pd–Au/HOPG samples up to 400 °C leads to alloy formation. • Contribution of parameters controlling the properties of Pd–Au alloyed particles has been discussed. - Abstract: The preparation of model bimetallic Pd–Au/HOPG catalysts has been investigated using scanning tunneling microscopy (STM) and X-ray photoelectron spectroscopy (XPS) techniques. Initially, model “core–shell” type Pd–Au/HOPG catalysts with similar particle size distribution (5–8 nm), but with different densities of particle locations on the HOPG surface and Pd/Au atomic ratios are prepared. Further, their thermal stability is studied within a temperature range of 50–500 °C at UHV conditions. It has been shown that annealing the model catalysts at a temperature range of 300–400 °C leads to formation of Pd–Au alloyed particles. Enhancement of heating temperature up to 500 °C results in sintering of bimetallic nanoparticles. Contribution of different parameters controlling the properties of Pd–Au alloyed particles has been discussed.

  11. Orthogonal experiment of a supported bimetallic catalyst prepared by homogeneous precipitation method*%均匀沉淀法制备负载型双金属催化剂的正交实验研究

    Institute of Scientific and Technical Information of China (English)

    别妙; 陈龙; 黄涛; 何贠; 罗凡; 李建芬

    2011-01-01

    以NiCl2·6H2O和Co(NO3)2·6H2O为原料,CO(NH2)2为沉淀剂,Al2O3为载体,采用均匀沉淀法制备了负载型双金属催化剂(Ni-Co/γ-Al2O3).利用正交实验探讨了不同工艺参数对催化剂合成的影响,并得出了最佳制备工艺.实验得出的最佳工艺参数为:n(NiCl2·6H2O)/n(Co(NO3)2·6H2O)为4∶1,n(CO(NH2)2)/n(Ni2+Co2+)为6∶1,均匀沉淀反应的温度和时间分别为115%和2.5h.同时运用XRD、SEM等分析手段对催化剂的物相结构和形貌进行了表征.结果显示催化剂外壳由复合的Ni-Co金属氧化物包裹,分散性良好,呈现多层立体结构.%The supported bimetallic catalysts (nano-Ni-Co/γ-Al2O3) were prepared by a homogeneous precipitation method involving an aqueous solution of nickel chloride hexahydrate, cobalt nitrate hexahydrate and urea, with alumina as the catalyst carrier. The effects of various technical parameters on the synthesis yield of catalysts were investigated and the optimum processing conditions were found through orthogonal experiments. The optimum processing conditions to prepare Ni-Co/γ-A12O3 bimetallic catalysts were as follows: the molar ratio of nickel chloride hexahydrate to cobalt nitrate hexahydrate was 4:1, the molar ratio of urea to metal salts was 6:1, the reaction temperature was 115℃, the reaction time was 2.5h. Different approaches such as XRD and SEM were adopted to characterize the crystalline structure and morphology of the supported catalysts. The analytical results indicated that the supported catalysts had the composite nanoparticle of nickel and cobalt oxide on the surfaee of γ-A12O3 carrier, which is a multi-layered structure with well dispersed.

  12. Distribution of platinum and cobalt atoms in a bimetallic nanoparticle

    Science.gov (United States)

    Chui, Yu Hang; Chan, Kwong-Yu

    2005-06-01

    Molecular dynamics simulations are performed to investigate the atomic distribution and the structure of platinum-cobalt nanoparticles. Heating and cooling techniques are applied before getting equilibrated structures at 298 K. Both crystalline (fcc) and amorphous structures are partly observed depending on cooling rates. The atomic distributions in different regions of a bimetallic nanoparticle are analyzed. Although platinum tends to occupy surface and near-surface sites of the bimetallic nanoparticle, a complete segregation to form a core-shell structure is not observed.

  13. The selective hydrogenation of crotonaldehyde over bimetallic catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Schoeb, Ann M. [Iowa State Univ., Ames, IA (United States)

    1997-10-17

    The selective hydrogenation of crotonaldehyde has been investigated over a monometallic Pt/SiO2 catalyst and platinum bimetallic catalysts where the second metal was either silver, copper, or tin. The effects of addition of a second metal to the Pt/SiO2 system on the selectivity to crotyl alcohol were investigated. The Pt-Sn bimetallic catalysts were characterized by hydrogen chemisorption, 1H NMR and microcalorimetry. The Pt-Ag/SiO2 and Pt-Cu/SiO2 catalysts were characterized by hydrogen chemisorption. Pt-Sn/SiO2 catalysts selectively hydrogenated crotonaldehyde to crotyl alcohol and the method of preparation of these catalysts affected the selectivity. The most selective Pt-Sn/SiO2 catalysts for the hydrogenation of crotonaldehyde to crotyl alcohol were those in which the Sn precursor was dissolved in a HCl solution. Sn increased both the rate of formation of butyraldehyde and the rate of formation of crotyl alcohol. The Pt/SiO2, Pt-Ag/SiO2 and Pt-Cu/SiO2 catalysts produced only butyraldehyde. Initial heats of adsorption (~90 kJ/mol) measured using microcalorimetry were not affected by the presence of Sn on Pt. We can conclude that there is no through metal electronic interaction between Pt and Sn at least with respect to hydrogen surface bonds since the Pt and Pt-Sn at least with respect to hydrogen surface bonds since the Pt and Pt-Sn had similar initial heats of adsorption coupled with the invariance of the 1H NMR Knight shift.

  14. Photoluminescence of hollow gold-silver bimetallic nanoparticles

    OpenAIRE

    Weon-Sik Chae; Hee-Ok Lee; Seung-Lim Oh

    2011-01-01

    Hollow gold nanoparticles including silver were prepared by the galvanic replacement reaction of silver nanoparticles by gold. The resulting hollow gold-silver bimetallic nanoparticles show notable blue-green emissions, which are studied using steady-state and time-resolved spectroscopy.

  15. Photoluminescence of hollow gold-silver bimetallic nanoparticles

    Directory of Open Access Journals (Sweden)

    Weon-Sik Chae

    2011-12-01

    Full Text Available Hollow gold nanoparticles including silver were prepared by the galvanic replacement reaction of silver nanoparticles by gold. The resulting hollow gold-silver bimetallic nanoparticles show notable blue-green emissions, which are studied using steady-state and time-resolved spectroscopy.

  16. Shift of localized surface plasmon resonance by Ar-ion irradiation of Ag–Au bimetallic films deposited on Al{sub 2}O{sub 3} single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Meng, Xuan [Graduate School of Engineering, Hokkaido University, Sapporo, Hokkaido 060-8628 (Japan); Shibayama, Tamaki, E-mail: shiba@qe.eng.hokudai.ac.jp [Center for Advanced Research of Energy and Materials, Faculty of Engineering, Hokkaido University, Kita-13, Nishi-8, Kita-ku, Sapporo, Hokkaido 060-8628 (Japan); Yu, Ruixuan; Takayanagi, Shinya [Graduate School of Engineering, Hokkaido University, Sapporo, Hokkaido 060-8628 (Japan); Watanabe, Seiichi [Center for Advanced Research of Energy and Materials, Faculty of Engineering, Hokkaido University, Kita-13, Nishi-8, Kita-ku, Sapporo, Hokkaido 060-8628 (Japan)

    2013-11-01

    Effects of Ar-ion induced surface nanostructuring were studied using 100 keV Ar-ion irradiation of 30 nm Ag–Au bimetallic films deposited on Al{sub 2}O{sub 3} single crystals, under irradiation fluences ranging from 5.0 × 10{sup 15} cm{sup −2} to 6.3 × 10{sup 16} cm{sup −2}. Scanning electron microscope was used to study the ion-beam-induced surface nanostructuring. As the irradiation fluence increased, dewetting of the bimetallic films on the Al{sub 2}O{sub 3} substrate was observed, and formation of isolated Ag–Au nanostructures sustained on the substrate were obtained. Next, thermal annealing was performed under high vacuum at 1073 K for 2 h; a layer of photosensitive Ag–Au alloy nanoballs partially embedded in the Al{sub 2}O{sub 3} substrate was obtained when higher fluence irradiation (>3.8 × 10{sup 16} cm{sup −2}) was used. The microstructures of the nanoballs were investigated using a transmission electron microscope, and the nanoballs were found to be single crystals with a FCC structure. In addition, photoabsorption spectra were measured, and localized surface plasmon resonance peaks were observed. With increase in the irradiation fluence, the size of the Ag–Au nanoballs on the substrate decreased, and a blue-shift of the LSPR peaks was observed. Further control of the LSPR frequency over a wide range was achieved by modifying the chemical components, and a red-shift of the LSPR peaks was observed as the Au concentration increased. In summary, ion irradiation is an effective approach toward surface nanostructuring, and the nanocomposites obtained have potential applications in optical devices.

  17. Using ionic liquid as the solvent to prepare Pd–Ni bimetallic nanoparticles by a pyrolysis method for ethanol oxidation reaction

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Keqiang, E-mail: dkeqiang@263.net [College of Chemistry and Materials Science, Hebei Normal University, Shijiazhuang 050024 (China); Yang, Hongwei; Cao, Yanli; Zheng, Chunbao [College of Chemistry and Materials Science, Hebei Normal University, Shijiazhuang 050024 (China); Rapole, Sowjanya B. [Integrated Composites Laboratory (ICL), Dan F. Smith Department of Chemical Engineering, Lamar University, Beaumont, TX 77710 (United States); Guo, Zhanhu, E-mail: zhanhu.guo@lamar.edu [Integrated Composites Laboratory (ICL), Dan F. Smith Department of Chemical Engineering, Lamar University, Beaumont, TX 77710 (United States)

    2013-10-01

    Room temperature ionic liquids (RTILs) of 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIBF4) is used as the solvent for the first time to prepare multi-walled carbon nanotubes (MWCNTs) supported nanocomposite catalysts of Pd{sub x}Ni{sub y} (atomic ratios of Pd to Ni are 1:1, 1:1.5, 1:2, and 1:2.5) nanoparticles (denoted as Pd{sub x}Ni{sub y}/MWCNTs) by using a simple pyrolysis process. The Pd{sub x}Ni{sub y}/MWCNTs catalysts are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Results show that the Pd{sub x}Ni{sub y} nanoparticles (NPs) are quite uniformly dispersed on the surface of MWCNTs with an average crystallite size of ∼7.0 nm. The electro-catalytic activity of the Pd{sub x}Ni{sub y}/MWCNTs catalysts for ethanol oxidation reaction (EOR) is examined by cyclic voltammetry (CV). It is revealed that the onset potential is ∼80 mV lower and the peak current is about three times higher for ethanol oxidation for MWCNT catalysts with Pd{sub 1}Ni{sub 1.5} compared to those of Pd/MWCNTs. The catalytic mechanisms of the Pd{sub 1}Ni{sub 1.5}/MWCNTs towards EOR are also proposed and discussed. - Highlights: • Introducing ionic liquids to the pyrolysis process for the preparation of Pd{sub x}Ni{sub y} nanoparticles. • Pd{sub x}Ni{sub y} nanoparticles with an average particle size of ∼7.0 nm were fabricated. • The peak current of EOR was about three times higher at Pd{sub 1}Ni{sub 1.5} compared to those of Pd.

  18. Bimetallic PtSn/C catalysts obtained via SOMC/M for glycerol steam reforming.

    Science.gov (United States)

    Pastor-Pérez, Laura; Merlo, Andrea; Buitrago-Sierra, Robison; Casella, Mónica; Sepúlveda-Escribano, Antonio

    2015-12-01

    A detailed study on the preparation of bimetallic PtSn/C catalysts using surface-controlled synthesis methods, and on their catalytic performance in the glycerol steam reforming reaction has been carried out. In order to obtain these well-defined bimetallic phases, techniques derived from Surface Organometallic Chemistry on Metals (SOMC/M) were used. The preparation process involved the reaction between an organometallic compound ((C4H9)4Sn) and a supported transition metal (Pt) in a H2 atmosphere. Catalysts with Sn/Pt atomic ratios of 0.2, 0.3, 0.5, and 0.7 were obtained, and characterized using several techniques: ICP, H2 chemisorption, TEM and XPS. These systems were tested in the glycerol steam reforming varying the reaction conditions (glycerol concentration and reaction temperature). The best performance was observed for the catalysts with the lowest tin contents (PtSn0.2/C and PtSn0.3/C). It was observed that the presence of tin increased the catalysts' stability when working under more severe reaction conditions.

  19. Specification guidelines for surface preparation of concrete prior to repair

    OpenAIRE

    Courard, Luc; Bissonnette, Benoît; Garbacz, Andrzej

    2017-01-01

    The repair of concrete requests specific preparation operations needed for guaranteeing compatibility between substrate and new materials as well as the development of adhesion properties. These specification guidelines contain design and construction recommendations for surface preparation of concrete for repair and overlay. The paper summarizes current knowledge, best practices and results of the research concerning the surface preparation of concrete prior to application of repair/overlay ...

  20. A DFT Structural Investigation of New Bimetallic PtSnx Surface Alloys Formed on the Pt(110) Surface and Their Interaction with Carbon Monoxide

    DEFF Research Database (Denmark)

    Zheng, Jian; Busch, Michael; Artiglia, Luca

    2016-01-01

    Two surface alloys with p(3 x 1) and p(6 x 1) periodicity have been identified after the deposition of metallic Sn on the (1 x 2)-Pt(110) surface. These two structures have been characterized by low energy electron diffraction (LEED), scanning tunneling microscopy (STM), and photoemission spectro...

  1. Laser Surface Preparation and Bonding of Aerospace Structural Composites

    Science.gov (United States)

    Belcher, M. A.; Wohl, C. J.; Hopkins, J. W.; Connell, J. W.

    2010-01-01

    Adhesive bonds are critical to the integrity of built-up structures. Disbonds can often be detected but the strength of adhesion between surfaces in contact is not obtainable without destructive testing. Typically the number one problem in a bonded structure is surface contamination, and by extension, surface preparation. Standard surface preparation techniques, including grit blasting, manual abrasion, and peel ply, are not ideal because of variations in their application. Etching of carbon fiber reinforced plastic (CFRP) panels using a neodymium-doped yttrium aluminum garnet (Nd:YAG) laser appears to be a highly precise and promising way to both clean a composite surface prior to bonding and provide a bond-promoting patterned surface akin to peel ply without the inherent drawbacks from the same (i.e., debris and curvature). CFRP surfaces prepared using laser patterns conducive to adhesive bonding were compared to typical prebonding surface treatments through optical microscopy, contact angle goniometry, and post-bonding mechanical testing.

  2. Preparation of superhydrophobic surfaces on cotton textiles

    Directory of Open Access Journals (Sweden)

    Chao-Hua Xue et al

    2008-01-01

    Full Text Available Superhydrophobic surfaces were fabricated by the complex coating of silica nanoparticles with functional groups onto cotton textiles to generate a dual-size surface roughness, followed by hydrophobization with stearic acid, 1H, 1H, 2H, 2H-perfluorodecyltrichlorosilane or their combination. The wettability and morphology of the as-fabricated surfaces were investigated by contact angle measurement and scanning electron microscopy. Characterizations by transmission electron microscopy, Fourier transformation infrared spectroscopy, and thermal gravimetric analysis were also conducted.

  3. Superamphiphobic Surfaces Prepared by Coating Multifunctional Nanofluids.

    Science.gov (United States)

    Esmaeilzadeh, Pouriya; Sadeghi, Mohammad Taghi; Bahramian, Alireza; Fakhroueian, Zahra; Zarbakhsh, Ali

    2016-11-23

    Construction of surfaces with the capability of repelling both water and oil is a challenging issue. We report the superamphiphobic properties of mineral surfaces coated with nanofluids based on synthesized Co-doped and Ce-doped Barium Strontium Titanate (CoBST and CeBST) nanoparticles and fluorochemicals of trichloro(1H,1H,2H,2H-perfluorooctyl)silane (PFOS) and polytetrafluoroethylene (PTFE). Coating surfaces with these nanofluids provides both oil (with surface tensions as low as 23 mN/m) and water repellency. Liquids with high surface tension (such as water and ethylene glycol) roll off the coated surface without tilting. A water drop released from 8 mm above the coated surface undergoes first a lateral displacement from its trajectory and shape deformation, striking the surface after 23 ms, bouncing and rolling off freely. These multifunctional coating nanofluids impart properties of self-cleaning. Applications include coating surfaces where cleanliness is paramount such as in hospitals and domestic environments as well as the maintenance of building facades and protection of public monuments from weathering. These superamphiphobic-doped nanofluids have thermal stability up to 180 °C; novel industrial applications include within fracking and the elimination of condensate blockage in gas reservoirs.

  4. Bimetallic Nanoparticles as Efficient Catalysts: Facile and Green Microwave Synthesis

    Directory of Open Access Journals (Sweden)

    Magda Blosi

    2016-07-01

    Full Text Available This work deals with the development of a green and versatile synthesis of stable mono- and bi-metallic colloids by means of microwave heating and exploiting ecofriendly reagents: water as the solvent, glucose as a mild and non-toxic reducer and polyvinylpirrolidone (PVP as the chelating agent. Particle size-control, total reaction yield and long-term stability of colloids were achieved with this method of preparation. All of the materials were tested as effective catalysts in the reduction of p-nitrophenol in the presence of NaBH4 as the probe reaction. A synergistic positive effect of the bimetallic phase was assessed for Au/Cu and Pd/Au alloy nanoparticles, the latter showing the highest catalytic performance. Moreover, monoand bi-metallic colloids were used to prepare TiO2- and CeO2-supported catalysts for the liquid phase oxidation of 5-hydroxymethylfufural (HMF to 2,5-furandicarboxylic acid (FDCA. The use of Au/Cu and Au/Pd bimetallic catalysts led to an increase in FDCA selectivity. Finally, preformed Pd/Cu nanoparticles were incorporated into the structure of MCM-41-silica. The resulting Pd/Cu MCM-41 catalysts were tested in the hydrodechlorination of CF3OCFClCF2Cl to CF3OCF=CF2. The effect of Cu on the hydrogenating properties of Pd was demonstrated.

  5. Preparation and formation mechanisms of metallic particles with controlled size, shape, structure and surface functionality

    Science.gov (United States)

    Lu, Lu

    Due to their excellent conductivity and chemical stability, particles of silver (Ag), gold (Au), copper (Cu) and their alloys are widely used in the electronic industry. Other unique properties extend their uses to the biomedical, optical and catalysis fields. All of these applications rely on particles with well controlled size, morphology, structure, and surface properties. Chemical precipitation from homogeneous solutions was selected as the synthetic route for the investigations described in this work. Based on the evaluation of key process parameters (temperature, reactant concentrations, reactant addition rate, mixing, etc.) the general formation mechanisms of metallic particles in various selected precipitation systems were investigated and elucidated. Five different systems for preparing particles with controlled size, morphology, structure and surface functionality are discussed. The first system involves the precipitation of Ag nanoparticles with spherical and anisotropic (platy or fiber-like) morphology. It will be shown that the formation of a stable Ag/Daxad complex has a significant impact on the reaction kinetics, and that the chromonic properties of Daxad molecules are responsible for the particle anisotropy. In the second system, Au-Ag core-shell nanoparticles were prepared in aqueous solution by a two-step precipitation process. The optical properties of these particles can be tailored by varying the thickness of the Ag shell. It was also determined that the stability of the bimetallic metallic sols depends on the Cl-ion concentration in solution. The third system discussed deals with preparation by the polyol process of well dispersed Cu nanospheres with high crystallinity and excellent oxidation resistance. We show that the heterogeneous nucleation (seeding) approach has significant merit in controlling particle size and uniformity. The functionalization of Au nanoparticle surfaces with glutathione molecules is discussed in the next section. The

  6. Comparing and Optimizing Nitrate Adsorption from Aqueous Solution Using Fe/Pt Bimetallic Nanoparticles and Anion Exchange Resins

    Directory of Open Access Journals (Sweden)

    Muhammad Daud

    2015-01-01

    Full Text Available This research work was carried out for the removal of nitrate from raw water for a drinking water supply. Nitrate is a widespread ground water contaminant. Methodology employed in this study included adsorption on metal based nanoparticles and ion exchange using anionic resins. Fe/Pt bimetallic nanoparticles were prepared in the laboratory, by the reduction of their respective salts using sodium borohydride. Scanning electron microscope, X-ray diffraction, energy dispersive spectrometry, and X-ray florescence techniques were utilized for characterization of bimetallic Fe/Pt nanoparticles. Optimum dose, pH, temperature, and contact time were determined for NO3- removal through batch tests, both for metal based nanoparticles and anionic exchange resin. Adsorption data fitted well the Langmuir isotherm and conformed to the pseudofirst-order kinetic model. Results indicated 97% reduction in nitrate by 0.25 mg/L of Fe/Pt nanoparticles at pH 7 and 83% reduction in nitrate was observed using 0.50 mg/L anionic exchange resins at pH 4 and contact time of one hour. Overall, Fe/Pt bimetallic nanoparticles demonstrated greater NO3- removal efficiency due to the small particle size, extremely large surface area (627 m2/g, and high adsorption capacity.

  7. Sample preparation for SEM of plant surfaces

    OpenAIRE

    A.K. Pathan; Bond, J.; R.E. Gaskin

    2010-01-01

    Plant tissues must be dehydrated for observation in most electron microscopes. Although a number of sample processing techniques have been developed for preserving plant tissues in their original form and structure, none of them are guaranteed artefact-free. The current paper reviews common scanning electron microscopy techniques and the sample preparation methods employed for visualisation of leaves under specific types of electron microscopes. Common artefacts introduced by specific techniq...

  8. Progress, Challenge, and Perspective of Bimetallic TiO2-Based Photocatalysts

    Directory of Open Access Journals (Sweden)

    Anna Zielińska-Jurek

    2014-01-01

    Full Text Available Bimetallic TiO2-based photocatalysts have attracted considerable attention in recent years as a class of highly active catalysts and photocatalysts under both UV and Vis light irradiation. Bimetallic noble metal structures deposited on TiO2 possess the ability to absorb visible light, in a wide wavelength range (broad LSPR peak, and therefore reveal the highest level of activity as a result of utilization of a large amount of incident photons. On the other hand they can enhance the rate of trapping photoexcited electrons and inhibit the recombination process due to the capability of the storage of photoexcited electrons. Based on literature two groups of bimetallic photocatalysts were distinguished. The first group includes bimetallic TiO2 photocatalysts (BMOX, highly active under UV and Vis light irradiation in a variety of oxidation reactions, and the second group presents bimetallic photocatalysts (BMRED exceptionally active in hydrogenation reactions. This review summarizes recent advances in the preparation and environmental application of bimetallic TiO2-based photocatalysts. Moreover, the effects of various parameters such as particle shape, size, amount of metals, and calcination on the photocatalytic activity of bimetallic TiO2-based photocatalysts are also discussed.

  9. Effects of Melt-to-Solid Insert Volume Ratio on the Microstructures and Mechanical Properties of Al/Mg Bimetallic Castings Produced by Lost Foam Casting

    Science.gov (United States)

    Jiang, Wenming; Fan, Zitian; Li, Guangyu; Yang, Li; Liu, Xinwang

    2016-12-01

    A356 aluminum and AZ91D magnesium alloys, which act as a solid insert and a melt, respectively, were used to prepare Al/Mg bimetallic castings using the lost-foam casting process, and the effects of the melt-to-solid volume ratio (VR) on the microstructures, mechanical properties, and fractographies of the Al/Mg bimetallic castings were investigated in this paper. Obtained results show that the average thickness of the reaction layer between aluminum and magnesium significantly increased with increasing VR, and a compact and uniform interface was obtained with a VR of 14.6. The reaction layers of all the bimetallic castings obtained by different VRs mainly consisted of the Al12Mg17 + δ eutectic layer close to the magnesium matrix, the Al12Mg17 + Mg2Si intermediate layer as well as the Al3Mg2 + Mg2Si layer next to the aluminum base. The microhardnesses of reaction layers of all the bimetallic castings with different VRs were considerably higher than those of the magnesium and aluminum matrix alloys, particularly the Al3Mg2 layer. Excessive thick reaction layer and pore defects remarkably weakened the bonding strength of the bimetallic castings, especially pore defects, and a relative maximum shear strength was obtained with a VR of 14.6. The fractographs of the push-out samples showed a change in the fracture surface from a mixed brittle and ductile fracture nature to that of a brittle fracture nature with the increase of VR.

  10. Charge distribution and Fermi level in bimetallic nanoparticles.

    Science.gov (United States)

    Holmberg, Nico; Laasonen, Kari; Peljo, Pekka

    2016-01-28

    Upon metal-metal contact, a transfer of electrons will occur between the metals until the Fermi levels in both phases are equal, resulting in a net charge difference across the metal-metal interface. Here, we have examined this contact electrification in bimetallic model systems composed of mixed Au-Ag nanoparticles containing ca. 600 atoms using density functional theory calculations. We present a new model to explain this charge transfer by considering the bimetallic system as a nanocapacitor with a potential difference equal to the work function difference, and with most of the transferred charge located directly at the contact interface. Identical results were obtained by considering surface contacts as well as by employing a continuum model, confirming that this model is general and can be applied to any multimetallic structure regardless of geometry or size (going from nano- to macroscale). Furthermore, the equilibrium Fermi level was found to be strongly dependent on the surface coverage of different metals, enabling the construction of scaling relations. We believe that the charge transfer due to Fermi level equilibration has a profound effect on the catalytic, electrocatalytic and other properties of bimetallic particles. Additionally, bimetallic nanoparticles are expected to have very interesting self-assembly for large superstructures due to the surface charge anisotropy between the two metals.

  11. Fabrication of electrically conductive nickel-silver bimetallic particles via polydopamine coating.

    Science.gov (United States)

    Kim, Sung Yeop; Kim, Jieun; Choe, Jaehoon; Byun, Young Chang; Seo, Jung Hyun; Kim, Do Hyun

    2013-11-01

    Inspired by adhesive proteins excreted by marine mussels, dopamine can act as a versatile surface modification agent for various organic and inorganic materials. By using adhesive polydopamine (PDA) as an intermediate layer, a simple and novel method for fabricating nickel-PDA-silver (Ni-PDA-Ag) bimetallic composite particles was developed. Ni-PDA-Ag bimetallic particles were fabricated by dispersing Ni particles in an aqueous dopamine solution followed by electroless Ag plating on the prepared Ni-PDA particles. A PDA layer with nano-meter thickness was deposited spontaneously on the surface of the Ni particles by oxidative self-polymerization of dopamine under alkaline conditions. Electroless Ag plating on the prepared Ni-PDA particles was carried out in the presence of a glucose solution as a reducing agent. Ni-PDA particles and Ni-PDA-Ag composite particles with a PDA intermediate layer were characterized by X-ray photoelectron spectroscopy (XPS), Fourier-transform infrared (FT-IR) spectroscopy, field-emission scanning electron microscopy (FE-SEM), field-emission transmission electron microscopy (FE-TEM), and X-ray diffraction (XRD). In addition, the electrical conductivity of as-prepared composite particles was evaluated by a 4-point probe. The PDA layer deposited on the surface of Ni was confirmed by XPS spectra, FT-IR spectroscopy, and FE-TEM. FE-SEM images demonstrated that Ag nanoparticles were successfully plated on the PDA layer-coated Ni particles after the electroless Ag plating process. XRD patterns also confirmed the presence of Ag in a metallic state. In addition, the sheet resistance of as-prepared composite particles showed a tendency to decrease with increasing AgNO3 concentration.

  12. An in-depth understanding of the bimetallic effects and coked carbon species on an active bimetallic Ni(Co)/Al2O3 dry reforming catalyst.

    Science.gov (United States)

    Liao, Xin; Gerdts, Rihards; Parker, Stewart F; Chi, Lina; Zhao, Yongxiang; Hill, Martyn; Guo, Junqiu; Jones, Martin O; Jiang, Zheng

    2016-06-29

    Ni/Al2O3, Co/Al2O3 and bimetallic Ni(Co)/Al2O3 catalysts were prepared using an impregnation method and employed in CO2 dry reforming of methane under coking-favored conditions. The spent catalysts were carefully characterized using typical characterization technologies and inelastic neutron scattering spectroscopy. The bimetallic catalyst exhibited a superior activity and anti-coking performance compared to Ni/Al2O3, while the most resistant to coking behavior was Co/Al2O3. The enhanced activity of the Ni(Co)/Al2O3 bimetallic catalyst is attributed to the reduced particle size of metallic species and resistance to forming stable filamentous carbon. The overall carbon deposition on the spent bimetallic catalyst is comparable to that of the spent Ni/Al2O3 catalyst, whereas the carbon deposited on the bimetallic catalyst is mainly less-stable carbonaceous species as confirmed by SEM, TPO, Raman and INS characterization. This study provides an in depth understanding of alloy effects in catalysts, the chemical nature of coked carbon on spent Ni-based catalysts and, hopefully, inspires the creative design of a new bimetallic catalyst for dry reforming reactions.

  13. Plasmonic Properties of Bimetallic Nanostructures and Their Applications in Hydrogen Sensing and Chemical Reactions

    Science.gov (United States)

    Jiang, Ruibin

    Noble metal nanocrystals have attracted great interest from a wide range of research fields because of their intriguing properties endowed by their localized surface plasmon resonances, which are the collective oscillations of free electrons. Under resonant excitation, metal nanostructures exhibit very large scattering and absorption cross sections and large near-field enhancement. These extraordinary properties can be used in different applications, such as plasmonic sensing and imaging, plasmon-controlled optics, photothermal therapy, photocatalysis, solar cells, and so on. Gold and Silver nanocrystals have plasmon resonances in the visible and near-infrared regions. However, gold and silver are not suitable for some applications. For example, they are generally inactive for catalyzing chemical reactions. The integration of plasmonic metals with other metals can offer superior or new physical/chemical properties. In this thesis, I prepared Au/Ag and Au/Pd bimetallic nanostructures and studied their plasmonic properties and applications in hydrogen sensing and photocatalysis. Seeds have a crucial importance in the synthesis of bimetallic nanostructures. I therefore first studied the roles of the crystalline structure and shape of seeds on the overgrowth of bimetallic nanostructures. The overgrowth of silver and palladium on single crystalline Au nanorods, multicrystalline Au nanorods, and nanobipyramids were studied under the same conditions for each metal. The growths of silver and palladium on single crystalline Au nanorods gave cuboidal nanostructures, while rod-shaped nanostructures were obtained from the growths of silver and palladium on multicrystalline Au nanorods and nanobipyramids. Moreover, the growths of silver and palladium on multicrystalline Au nanobipyramids started at the stepped side facets, while the growths started at the twin boundaries on multicrystalline Au nanorods. These results unambiguously indicate that the crystalline structure of

  14. Salt flux synthesis of single and bimetallic carbide nanowires

    Science.gov (United States)

    Leonard, Brian M.; Waetzig, Gregory R.; Clouser, Dale A.; Schmuecker, Samantha M.; Harris, Daniel P.; Stacy, John M.; Duffee, Kyle D.; Wan, Cheng

    2016-07-01

    Metal carbide compounds have a broad range of interesting properties and are some of the hardest and highest melting point compounds known. However, their high melting points force very high reaction temperatures and thus limit the formation of high surface area nanomaterials. To avoid the extreme synthesis temperatures commonly associated with these materials, a new salt flux technique has been employed to reduce reaction temperatures and form these materials in the nanometer regime. Additionally, the use of multiwall carbon nanotubes as a reactant further reduces the diffusion distance and provides a template for the final carbide materials. The metal carbide compounds produced through this low temperature salt flux technique maintain the nanowire morphology of the carbon nanotubes but increase in size to ˜15-20 nm diameter due to the incorporation of metal in the carbon lattice. These nano-carbides not only have nanowire like shape but also have much higher surface areas than traditionally prepared metal carbides. Finally, bimetallic carbides with composition control can be produced with this method by simply using two metal precursors in the reaction. This method provides the ability to produce nano sized metal carbide materials with size, morphology, and composition control and will allow for these compounds to be synthesized and studied in a whole new size and temperature regime.

  15. Preparation and characterization of low-defect surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Robinson, T.O.

    1991-12-01

    Silver crystal surfaces with low defect densities were prepared electrochemically from aqueous solutions using capillary-growth techniques. These surfaces had low rates for the nucleation of new silver layers. The impedance of these inert silver/aqueous silver nitrate interfaces was used to determine silver adatom concentration and water dipole reorientation energetics.

  16. Nanosegregated bimetallic oxide anode catalyst for proton exchange membrane electrolyzer

    Science.gov (United States)

    Danilovic, Nemanja; Kang, Yijin; Markovic, Nenad; Stamenkovic, Vojislav; Myers, Deborah J.; Subbaraman, Ram

    2016-08-23

    A surface segregated bimetallic composition of the formula Ru.sub.1-xIr.sub.x wherein 0.1.ltoreq.x.ltoreq.0.75, wherein a surface of the material has an Ir concentration that is greater than an Ir concentration of the material as a whole is provided. The surface segregated material may be produced by a method including heating a bimetallic composition of the formula Ru.sub.1-xIr.sub.x, wherein 0.1.ltoreq.x.ltoreq.0.75, at a first temperature in a reducing environment, and heating the composition at a second temperature in an oxidizing environment. The surface segregated material may be utilized in electrochemical devices.

  17. Synthesis of Supported NiPt Bimetallic Nanoparticles, Methods for Controlling the Surface Coverage of Ni Nanoparticles With Pt, Methods Of Making NiPt Multilayer Core-Shell Structures and Application of the Supported Catalysts for CO2 Reforming

    KAUST Repository

    Li, Lidong

    2015-06-25

    Embodiments of the present disclosure provide for supported Ni/Pt bimetallic nanoparticles, compositions including supported NiPt nanoparticles, methods of making supported NiPt nanoparticles, methods of using supported NiPt nanoparticles, and the like.

  18. Effect of preparation conditions on physicochemical, surface and catalytic properties of cobalt ferrite prepared by coprecipitation

    Energy Technology Data Exchange (ETDEWEB)

    El-Shobaky, G.A., E-mail: elshobaky@yahoo.co [Physical Chemistry Department, National Research Center, Dokki, Cairo (Egypt); Turky, A.M.; Mostafa, N.Y.; Mohamed, S.K. [Chemistry Department, Faculty of Science, Suez Canal University, Ismailia 41522 (Egypt)

    2010-03-18

    Cobalt ferrite nanoparticles were prepared via thermal treatment of cobalt-iron mixed hydroxides at 400-600 {sup o}C. The mixed hydroxides were coprecipitated from their nitrates solutions using NaOH as precipitating agent. The effects of pH and temperature of coprecipitation and calcination temperature on the physicochemical, surface and catalytic properties of the prepared ferrites were studied. The prepared systems were characterized using TG, DTG, DTA, chemical analysis, atomic absorption spectroscopy (AAS), X-ray diffraction (XRD), energy dispersive X-ray (EDX) as well as surface and texture properties based on nitrogen adsorption-desorption isotherms. The prepared cobalt ferrites were found to be mesoporous materials that have crystallite size ranges between 8 and 45 nm. The surface and catalytic properties of the produced ferrite phase were strongly dependent on coprecipitation conditions of the mixed hydroxides and on their calcination temperature.

  19. Hydrogen production using Ag-Pd/TiO2 bimetallic catalysts: is there a combined effect of surface plasmon resonance with the Schottky mechanism on the photo-catalytic activity?(Conference Presentation)

    Science.gov (United States)

    Nadeem, Muhammad Amtiaz; Idriss, Hicham; Al-Oufi, Maher; Ahmed, Khaja Wahab; Anjum, Dalaver H.

    2016-10-01

    A series of Ag-Pd/TiO2 catalysts have been prepared, characterized and tested for H2 production activities from water in the presence of organic sacrificial agents. The synergistic effect of metallic properties (plasmonic and Schottky mechanisms) was investigated. XPS results indicated that silver is present in the form of its oxides (Ag2O and AgO) at 0.2-0.4 wt. % loading while palladium is present as PdO and Pd metal at similar loading. However, metallic character for silver particles increases while that of palladium metal particles decreases with increasing their % in the investigated range (0-1 wt. %). HRTEM results coupled with EDX analyses indicated the presence of two types of Ag containing particles (large ones with about 4-6 nm and smaller ones with ca. 1nm in size). Palladium was only found forming Ag-Pd alloy/composite with a wide size distribution range between 10-60 nm. Both particles are composed of silver and palladium, however. Optimal photocatalytic H2 production rates were obtained for catalysts with a palladium to silver ratios between 4 and 1.5 in the case of bimetallic catalysts. In addition, H2 production rates showed linear dependency on plasmonic response of Ag. The study demonstrates that increased H2 production rates can be achieved from an understanding of plasmonic and Schottky properties of metals loaded on top of the semiconductor.

  20. Fe/Al bimetallic particles for the fast and highly efficient removal of Cr(VI) over a wide pH range: Performance and mechanism.

    Science.gov (United States)

    Fu, Fenglian; Cheng, Zihang; Dionysiou, Dionysios D; Tang, Bing

    2015-11-15

    The iron/aluminum (Fe/Al) bimetallic particles with high efficiency for the removal of Cr(VI) were prepared. Fe/Al bimetallic particles were characterized by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), SEM mapping, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). SEM mapping showed that the core of bimetal was Al, and the planting Fe was deposited on the surface of Al. In acidic and neutral conditions, Fe/Al bimetal can completely remove Cr(VI) from wastewater in 20 min. Even at pH 11.0, the Cr(VI) removal efficiency achieved was 93.5%. Galvanic cell effect and high specific surface area are the main reasons for the enhanced removal of Cr(VI) by bimetallic particles. There were no iron ions released in solutions at pH values ranging from 3.0 to 11.0. The released Al(3+) ions concentrations in acidic and neutral conditions were all less than 0.2mg/L. The bimetal can be used 4 times without losing activity at initial pH 3.0. XPS indicated that the removed Cr(VI) was immobilized via the formation of Cr(III) hydroxide and Cr(III)-Fe(III) hydroxide/oxyhydroxide on the surface of Fe/Al bimetal. The Fe/Al bimetallic particles are promising for further testing for the rapid and effective removal of contaminants from water. Copyright © 2015 Elsevier B.V. All rights reserved.

  1. Laser Surface Preparation for Adhesive Bonding of Aerospace Structural Composites

    Science.gov (United States)

    Belcher, M. A.; Wohl, C. J.; Hopkins, J. W.; Connell, J. W.

    2010-01-01

    Adhesive bonds are critical to the integrity of built-up structures. Disbonds can often be detected but the strength of adhesion between surfaces in contact is not obtainable without destructive testing. Typically the number one problem in a bonded structure is surface contamination, and by extension, surface preparation. Standard surface preparation techniques, including grit blasting, manual abrasion, and peel ply, are not ideal because of variations in their application. Etching of carbon fiber reinforced plastic (CFRP) panels using a neodymium-doped yttrium aluminum garnet (Nd:YAG) laser appears to be a highly precise and promising way to both clean a composite surface prior to bonding and provide a bond-promoting patterned surface akin to peel ply without the inherent drawbacks from the same (i.e., debris and curvature). CFRP surfaces prepared using laser patterns conducive to adhesive bonding were compared to typical pre-bonding surface treatments through optical microscopy, contact angle goniometry, and post-bonding mechanical testing.

  2. Toward atomically-precise synthesis of supported bimetallic nanoparticles using atomic layer deposition.

    Science.gov (United States)

    Lu, Junling; Low, Ke-Bin; Lei, Yu; Libera, Joseph A; Nicholls, Alan; Stair, Peter C; Elam, Jeffrey W

    2014-01-01

    Multi-metallic nanoparticles constitute a new class of materials offering the opportunity to tune the properties via the composition, atomic ordering and size. In particular, supported bimetallic nanoparticles have generated intense interest in catalysis and electrocatalysis. However, traditional synthesis methods often lack precise control, yielding a mixture of monometallic and bimetallic particles with various compositions. Here we report a general strategy for synthesizing supported bimetallic nanoparticles by atomic layer deposition, where monometallic nanoparticle formation is avoided by selectively growing the secondary metal on the primary metal nanoparticle but not on the support; meanwhile, the size, composition and structure of the bimetallic nanoparticles are precisely controlled by tailoring the precursor pulse sequence. Such exquisite control is clearly demonstrated through in situ Fourier transform infrared spectroscopy of CO chemisorption by mapping the gradual atomic-scale evolution in the surface composition, and further confirmed using aberration-corrected scanning transmission electron microscopy.

  3. Levelling the playing field: screening for synergistic effects in coalesced bimetallic nanoparticles.

    Science.gov (United States)

    Tan, Rachel Lee Siew; Song, Xiaohui; Chen, Bo; Chong, Wen Han; Fang, Yin; Zhang, Hua; Wei, Jun; Chen, Hongyu

    2016-02-14

    Depending on the synthetic methods, bimetallic nanoparticles can have either core-shell, phase segregated, alloy, or partially coalesced structures, presenting different degrees of atomic mixing on their surface. Along with the variations of size and morphology, the structural differences make it difficult to compare the catalytic activity of bimetallic nanoparticles. In this article, we developed a facile screening method that can focus on the synergistic effects rather than structural differences. Prefabricated nanoparticles are mixed together to form linear aggregates and coalesced to form bimetallic junctions. Their hollow silica shells allow materials transport but prevent further aggregation. With a level playing field, this screening platform can identify the best bimetallic combination for a catalytic reaction, before optimizing the synthesis. This approach is more advantageous than the conventional approaches where structural difference may have dominant effects on the catalytic performance.

  4. Cu-Sn Bimetallic Catalyst for Selective Aqueous Electroreduction of CO2 to CO

    KAUST Repository

    Sarfraz, Saad

    2016-03-23

    We report a selective and stable electrocatalyst utilizing non-noble metals consisting of Cu and Sn for the efficient and selective reduction of CO2 to CO over a wide potential range. The bimetallic electrode was prepared through the electrodeposition of Sn species on the surface of oxide-derived copper (OD-Cu). The Cu surface, when decorated with an optimal amount of Sn, resulted in a Faradaic efficiency (FE) for CO greater than 90% and a current density of −1.0 mA cm−2 at −0.6 V vs. RHE, compared to the CO FE of 63% and −2.1 mA cm−2 for OD-Cu. Excess Sn on the surface caused H2 evolution with a decreased current density. X-ray diffraction (XRD) suggests the formation of Cu-Sn alloy. Auger electron spectroscopy of the sample surface exhibits zero-valent Cu and Sn after the electrodeposition step. Density functional theory (DFT) calculations show that replacing a single Cu atom with a Sn atom leaves the d-band orbitals mostly unperturbed, signifying no dramatic shifts in the bulk electronic structure. However, the Sn atom discomposes the multi-fold sites on pure Cu, disfavoring the adsorption of H and leaving the adsorption of CO relatively unperturbed. Our catalytic results along with DFT calculations indicate that the presence of Sn on reduced OD-Cu diminishes the hydrogenation capability—i.e., the selectivity towards H2 and HCOOH—while hardly affecting the CO productivity. While the pristine monometallic surfaces (both Cu and Sn) fail to selectively reduce CO2, the Cu-Sn bimetallic electrocatalyst generates a surface that inhibits adsorbed H*, resulting in improved CO FE. This study presents a strategy to provide a low-cost non-noble metals that can be utilized as a highly selective electrocatalyst for the efficient aqueous reduction of CO2.

  5. Characterisation of the surface of freshly prepared precious metal catalysts.

    Science.gov (United States)

    Parker, Stewart F; Adroja, Devashibhai; Jiménez-Ruiz, Mónica; Tischer, Markus; Möbus, Konrad; Wieland, Stefan D; Albers, Peter

    2016-07-14

    A combination of electron microscopy, X-ray and neutron spectroscopies and computational methods has provided new insights into the species present on the surface of freshly prepared precious metal catalysts. The results show that in all cases, at least half of the surface is metallic or nearly so, with the remainder covered by oxygen, largely as hydroxide. Water is also present and is strongly held; weeks of pumping under high vacuum is insufficient to remove it. The hydroxyls are reactive as shown by their reaction with or displacement by CO and can be removed by hydrogenation. This clearly has implications for how precious metal catalysts are activated after preparation.

  6. Gas-Phase Growth of Heterostructures of Carbon Nanotubes and Bimetallic Nanowires

    Directory of Open Access Journals (Sweden)

    Whi Dong Kim

    2011-01-01

    Full Text Available A simple, inexpensive, and viable method for growing multiple heterostructured carbon nanotubes (CNTs over the entire surface of Ni-Al bimetallic nanowires (NWs in the gas phase was developed. Polymer-templated bimetallic nitrate NWs were produced by electrospinning in the first step, and subsequent calcination resulted in the formation of bimetallic oxide NWs by thermal decomposition. In the second step, free-floating bimetallic NWs were produced by spray pyrolysis in an environment containing hydrogen gas as a reducing gas. These NWs were continuously introduced into a thermal CVD reactor in order to grow CNTs in the gas phase. Scanning electron microscopy (SEM, transmission electron microscopy (TEM, and Raman spectrometry analyses revealed that the catalytic Ni sites exposed in the non-catalytic Al matrix over the entire surface of the bimetallic NWs were seeded to radially grow highly graphitized CNTs, which resembled “foxtail” structures. The grown CNTs were found to have a relatively uniform diameter of approximately 10±2 nm and 10 to 15 walls with a hollow core. The average length of the gas-phase-grown CNTs can be controlled between 100 and 1000 nm by adjusting the residence time of the free-floating bimetallic NWs in the thermal CVD reactor.

  7. Fe/Al bimetallic particles for the fast and highly efficient removal of Cr(VI) over a wide pH range: Performance and mechanism

    Energy Technology Data Exchange (ETDEWEB)

    Fu, Fenglian, E-mail: fufenglian2006@163.com [School of Environmental Science and Engineering, Guangdong University of Technology, Guangzhou 510006 (China); Environmental Engineering and Science Program, Department of Biomedical, Chemical and Environmental Engineering (DBCEE), University of Cincinnati, OH 45221-0012 (United States); Cheng, Zihang [School of Environmental Science and Engineering, Guangdong University of Technology, Guangzhou 510006 (China); Dionysiou, Dionysios D., E-mail: dionysios.d.dionysiou@uc.edu [Environmental Engineering and Science Program, Department of Biomedical, Chemical and Environmental Engineering (DBCEE), University of Cincinnati, OH 45221-0012 (United States); Tang, Bing [School of Environmental Science and Engineering, Guangdong University of Technology, Guangzhou 510006 (China)

    2015-11-15

    Highlights: • Bimetallic particles with different Fe/Al mass ratios were prepared. • High removal rate of Cr(VI) was achieved in acidic, neutral, and alkaline pH. • No total iron ions at pH 3.0–11.0 and nearly no Al{sup 3+} at pH 3.0–7.0 were released. • Galvanic cell effect and high specific surface area contributed to Cr(VI) removal. - Abstract: The iron/aluminum (Fe/Al) bimetallic particles with high efficiency for the removal of Cr(VI) were prepared. Fe/Al bimetallic particles were characterized by scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), SEM mapping, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). SEM mapping showed that the core of bimetal was Al, and the planting Fe was deposited on the surface of Al. In acidic and neutral conditions, Fe/Al bimetal can completely remove Cr(VI) from wastewater in 20 min. Even at pH 11.0, the Cr(VI) removal efficiency achieved was 93.5%. Galvanic cell effect and high specific surface area are the main reasons for the enhanced removal of Cr(VI) by bimetallic particles. There were no iron ions released in solutions at pH values ranging from 3.0 to 11.0. The released Al{sup 3+} ions concentrations in acidic and neutral conditions were all less than 0.2 mg/L. The bimetal can be used 4 times without losing activity at initial pH 3.0. XPS indicated that the removed Cr(VI) was immobilized via the formation of Cr(III) hydroxide and Cr(III)–Fe(III) hydroxide/oxyhydroxide on the surface of Fe/Al bimetal. The Fe/Al bimetallic particles are promising for further testing for the rapid and effective removal of contaminants from water.

  8. Bimetallic Au-decorated Pd catalyst for the liquid phase hydrodechlorination of 2,4-dichlorophenol

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Juan [School of the Environment, Donghua University, Shanghai 201620 (China); Chen, Huan, E-mail: hchen404@njust.edu.cn [Key Laboratory of Jiangsu Province for Chemical Pollution Control and Resources Reuse, School of Environmental & Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094 (China); Chen, Quanyuan; Huang, Zhaolu [School of the Environment, Donghua University, Shanghai 201620 (China)

    2016-11-30

    Graphical abstract: 2,4-Dichlorophenol can be converted to phenol via the catalytic HDC method over Pd-Au/CNTs and the catalytic activity first increased and then decreased with Au content. - Highlights: • Bimetallic catalysts had smaller metal particles and larger number of exposed active site than the monometallic catalysts. • The cationization of Pd particles increased with Au content in the bimetallic catalysts. • The bimetallic catalysts exhibited higher catalytic activities for HDC of 2,4-DCP than the monometallic counterparts. • The concerted pathway for HDC of 2,4-DCP was more predominant with increasing Au content in the bimetallic catalyst. - Abstract: Monometallic and bimetallic Pd-Au catalysts supported on multi-walled carbon nanotubes (CNTs) with varied Au cooperation amounts were prepared using the complexing-reduction method in the presence of tetrahydrofuran (THF). The liquid phase catalytic hydrodechlorination (HDC) of 2,4-dichlorophenol (2,4-DCP) was investigated over these bimetallic catalysts. The catalysts were characterized by N{sub 2} adsorption-desorption isotherms, X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, and H{sub 2} chemisorption. Characterization results showed that the co-reduction of Pd and Au mainly formed alloy-like structure. The bimetallic catalysts had smaller metal particles and larger numbers of exposed active site than that of monometallic catalysts. In addition, compared with Pd(1.7)/CNTs and Au(0.4)/CNTs, the binding energies of Pd 3d{sub 5/2} shifted to higher positions while that of Au 4f{sub 7/2} had negative shifts in the Pd-Au bimetallic catalysts, which can be ascribed to the electrons transferred from metal Pd to Au and the cationization of Pd particles was enhanced. Accordingly, the bimetallic Pd-Au particles with different Au contents in the catalysts exhibited varied synergistic effects for the catalytic HDC of 2,4-DCP, with Pd(1.8)Au(0.4)/CNTs having the highest

  9. STM characterization of MOVPE-prepared silicon surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Kleinschmidt, Peter; Brueckner, Sebastian; Luczak, Johannes; Supplie, Oliver; Dobrich, Anja; Doescher, Henning; Hannappel, Thomas [Helmholtz-Zentrum Berlin fuer Materialien und Energie, Hahn-Meitner-Platz 1, 14109 Berlin (Germany)

    2011-07-01

    The clean Si(100) surface reconstructs by forming dimers, thus reducing the number of dangling bonds at the surface. In the MOVPE environment hydrogen is commonly used as process gas, which leads to a monohydride silicon surface with a 2 x 1 unit cell consisting of H-Si-Si-H dimers. Even so, the quality of the surface can vary dramatically depending on process conditions. In general, annealing in hydrogen leads to a two-domain surface structure with monoatomic steps, where the resulting structure also strongly depends on misorientation. We find process conditions for preparation of Si(100) surfaces with 0.1 , 2 and 6 offcut where a strong preference for one domain is obtained, making the resulting surfaces ideal substrates for III-V-on-Si epitaxy. A process consisting of deoxidation, homoepitaxial buffer layer growth and annealing is found to result in D{sub A}-type double layer steps for 0.1 , and D{sub B}-type double layer steps for 6 offcut. The identical process leads to single layer steps for 2 offcut. Here, we obtain D{sub A}-type double layer steps by a modified process which includes a slow cooling phase after the annealing step. Our results, verified by scanning tunneling microscopy, low energy electron diffraction and Fourier-transform infrared spectroscopy, are in sharp contrast to the clean and the hydrogenated Si(100) surface prepared in UHV.

  10. HIGH VELOCITY THERMAL GUN FOR SURFACE PREPARATION AND TREATMENT

    Directory of Open Access Journals (Sweden)

    I.A. Gorlach

    2012-01-01

    Full Text Available Many surface preparation and treatment processes utilise compressed air to propel particles against surfaces in order to clean and treat them. The effectiveness of the processes depends on the velocity of the particles, which in turn depends on the pressure of the compressed air. This paper describes a thermal gun built on the principles of High Velocity Air Fuel (HVAF and High Velocity Oxy Fuel (HVOF processes. The designed apparatus can be used for abrasive blasting, coating of surfaces, cutting of rocks, removing rubber from mining equipment, cleaning of contaminations etc.

  11. Characterization and reactivity of Pd Pt bimetallic supported catalysts obtained by laser vaporization of bulk alloy

    Science.gov (United States)

    Rousset, J. L.; Cadete Santos Aires, F. J.; Bornette, F.; Cattenot, M.; Pellarin, M.; Stievano, L.; Renouprez, A. J.

    2000-09-01

    Bimetallic Pd-Pt clusters produced by laser vaporization of bulk alloy have been deposited on high surface alumina. Energy dispersive X-ray (EDX) analysis and transmission electron microscopy (TEM) show that they have a perfectly well-defined stoichiometry and a narrow range of size. Therefore, they constitute ideal systems to investigate alloying effects towards reactivity. Pd-Pt alloys are already known for their applications in the hydrogenation of unsaturated hydrocarbons, especially aromatics, because this system is highly resistant to sulfur and nitrogen poisoning. In this context, the catalytic properties of this system have been investigated in the hydrogenation of tetralin in the presence of hydrogen sulfide. Preliminary results show that this model catalyst is more sulfur-resistant than each of the pure supported metals prepared by chemical methods.

  12. Glycerol conversion into value added chemicals over bimetallic catalysts in supercritical carbon dioxide

    Science.gov (United States)

    Hidayati, Luthfiana N.; Sudiyarmanto, Adilina, Indri B.

    2017-01-01

    Development of alternative energy from biomass encourage the experiments and production of biodiesel lately. Biodiesel industries widely expand because biodiesel as substitute of fossil fuel recognized as promising renewable energy. Glycerol is a byproduct of biodiesel production, which is resulted 10% wt average every production. Meanwhile, carbon dioxide is a gas that is very abundant amount in the atmosphere. Glycerol and carbon dioxide can be regarded as waste, possibly will produce value-added chemical compounds through chemically treated. In this preliminary study, conversion of glycerol and carbon dioxide using bimetallic catalyst Ni-Sn with various catalyst supports : MgO, γ-Al2O3, and hydrotalcite. Catalysts which have been prepared, then physically characterized by XRD, surface area and porosity analysis, and thermal gravity analysis. Catalytic test performance using supercritical carbon dioxide conditions. Furthermore, the products were analyzed by GC. The final product mostly contained of propylene glycol and glycerol carbonate.

  13. The quality of the joint between alloy steel and unalloyed cast steel in bimetallic layered castings

    Directory of Open Access Journals (Sweden)

    T. Wróbel

    2012-01-01

    Full Text Available In paper is presented technology of bimetallic layered castings based on founding method of layer coating directly in cast process so-called method of mould cavity preparation. Prepared castings consist two fundamental parts i.e. bearing part and working part (layer. The bearing part of bimetallic layered casting is typical foundry material i.e. ferritic-pearlitic unalloyed cast steel, whereas working part (layer is plate of austenitic alloy steel sort X2CrNi 18-9. The ratio of thickness between bearing and working part is 8:1. The aim of paper was assessed the quality of the joint between bearing and working part in dependence of pouring temperature and carbon concentration in cast steel. The quality of the joint in bimetallic layered castings was evaluated on the basis of ultrasonic non-destructive testing, structure and microhardness researches.

  14. One-pot wet-chemical co-reduction synthesis of bimetallic gold-platinum nanochains supported on reduced graphene oxide with enhanced electrocatalytic activity

    Science.gov (United States)

    Chen, De-Jun; Zhang, Qian-Li; Feng, Jin-Xia; Ju, Ke-Jian; Wang, Ai-Jun; Wei, Jie; Feng, Jiu-Ju

    2015-08-01

    In this work, a simple, rapid and facile one-pot wet-chemical co-reduction method is developed for synthesis of bimetallic Au-Pt alloyed nanochains supported on reduced graphene oxide (Au-Pt NCs/RGO), in which caffeine is acted as a capping agent and a structure-directing agent, while no any seed, template, surfactant or polymer involved. The as-prepared nanocomposites display enlarged electrochemical active surface area, significantly enhanced catalytic activity and better stability for methanol and ethylene glycol oxidation, compared with commercial Pt-C (Pt 50 wt%), PtRu-C (Pt 30 wt% and Ru 15 wt%) and Pt black.

  15. Controlled synthesis and synergistic effects of graphene-supported PdAu bimetallic nanoparticles with tunable catalytic properties.

    Science.gov (United States)

    Liu, Chang-Hai; Liu, Rui-Hua; Sun, Qi-Jun; Chang, Jian-Bing; Gao, Xu; Liu, Yang; Lee, Shuit-Tong; Kang, Zhen-Hui; Wang, Sui-Dong

    2015-04-14

    Graphene-supported bimetallic nanoparticles are promising nanocatalysts, which can show strong and tunable catalytic activity and selectivity. Herein room-temperature-ionic-liquid-assisted metal sputtering is utilized to synthesize PdAu bimetallic nanoparticles on graphene with bare surface, small size, high surface density and controlled Pd-to-Au ratio. This controllable synthetic approach is green-chemistry compatible and totally free of additives and byproducts. The supported PdAu nanoparticles show excellent catalytic capabilities for both oxidation and reduction reactions, strongly dependent on the Pd-to-Au ratio. A strong correlation among catalytic performance, bimetallic composition and charge redistribution in the PdAu nanoparticles has been demonstrated. The results suggest that sufficient Au d-holes appear to be significant to the catalysis of oxidation reaction, and a metallic Pd surface is critical to the catalysis of reduction reaction. By the present method, the bimetallic combination can be tailored for distinct types of catalytic reactions.

  16. Extended X-ray absorption fine structure of bimetallic nanoparticles

    Directory of Open Access Journals (Sweden)

    Carolin Antoniak

    2011-05-01

    Full Text Available Electronic and magnetic properties strongly depend on the structure of the material, especially on the crystal symmetry and chemical environment. In nanoparticles, the break of symmetry at the surface may yield different physical properties with respect to the corresponding bulk material. A useful tool to investigate the electronic structure, magnetic behaviour and local crystallographic structure is X-ray absorption spectroscopy. In this review, recent developments in the field of extended X-ray absorption fine structure measurements and in the analysis methods for structural investigations of bimetallic nanoparticles are highlighted. The standard analysis based on Fourier transforms is compared to the relatively new field of wavelet transforms that have the potential to outperform traditional analysis, especially in bimetallic alloys. As an example, the lattice expansion and inhomogeneous alloying found in FePt nanoparticles is presented, and this is discussed below in terms of the influence of employed density functional theory calculations on the magnetic properties.

  17. Disturbance induced by surface preparation on instrumented indentation test

    Energy Technology Data Exchange (ETDEWEB)

    Li, Yugang, E-mail: yugang.li@utt.fr [Université de Technologie de Troyes (UTT), ICD-LASMIS, UMR CNRS 6281, 12, rue Marie Curie-CS 42060, 10010 Troyes Cedex (France); Kanouté, Pascale, E-mail: pascale.kanoute@onera.fr [Université de Technologie de Troyes (UTT), ICD-LASMIS, UMR CNRS 6281, 12, rue Marie Curie-CS 42060, 10010 Troyes Cedex (France); The French Aerospace Lab (ONERA), DMSM/MCE, 29 avenue de la Division Leclerc-BP 72, F-92322 Chatillon Cedex (France); François, Manuel, E-mail: manuel.francois@utt.fr [Université de Technologie de Troyes (UTT), ICD-LASMIS, UMR CNRS 6281, 12, rue Marie Curie-CS 42060, 10010 Troyes Cedex (France)

    2015-08-26

    Surface preparation, which may induce considerable sample disturbance, plays an important role in instrumented indentation test (IIT). In this study, the sample disturbance (mainly divided into residual stresses and plastic strain) induced by the surface preparation process of instrumented indentation test specimens were investigated with both experimental tests and numerical simulations. Grazing incidence X-ray diffractions (GIXRD) and uniaxial tensile tests were conducted for characterizing the residual stresses and high plastic strain in the top surface layers of a carefully mechanically polished indentation sample, which, in the present work, is made of commercially pure titanium. Instrumented indentation tests and the corresponding finite element simulations were performed as well. For comparison, a reference sample (carefully mechanically polished & electrolytically polished) which represents the raw material was prepared and tested. Results showed that a careful mechanical polishing procedure can effectively reduce the level of residual stresses induced by this process. However, the high plastic strain in the surface region imposed by the polishing process is significant. The induced plastic strain can affect a depth up to 5 µm, which is deeper than the maximum penetration depth h{sub max} (3 µm) used for the instrumented indentation tests. In the near surface layer (in the range of depth about 350 nm), the plastic strain levels are fairly high. In the very top layer, the plastic strain was even estimated to reach more than 60%. The simultaneous use of indentation tests and numerical simulations showed that the existence of high plastic strain in the surface region will make the load vs depth (P–h) curve shift upwards, the contact hardness (H) increase and the contact stiffness (S) decrease.

  18. Synthesis by Microwaves of Bimetallic Nano-Rhodium-Palladium

    Directory of Open Access Journals (Sweden)

    M. Ugalde

    2013-01-01

    Full Text Available An improved acrylamide sol-gel technique using a microwave oven in order to synthesize bimetallic Rh-Pd particles is reported and discussed. The synthesis of Pd and Rh nanoparticles was carried out separately. The polymerization to form the gel of both Rh and Pd was carried out at 80°C under constant agitations. The method chosen to prepare the Rh and Pd xerogels involved the decomposition of both gels. The process begins by steadily increasing the temperature of the gel inside a microwave oven (from 80°C to 170°C. In order to eliminate the by-products generated during the sol-gel reaction, a heat treatment at a temperature of 1000°C for 2 h in inert atmosphere was carried out. After the heat treatment, the particle size increased from 50 nm to 200 nm, producing the bimetallic Rh-Pd clusters. It can be concluded that the reported microwave-assisted, sol-gel method was able to obtain nano-bimetallic Rh-Pd particles with an average size of 75 nm.

  19. Facile preparation of superhydrophobic surfaces based on metal oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Bao, Xue-Mei; Cui, Jin-Feng; Sun, Han-Xue; Liang, Wei-Dong; Zhu, Zhao-Qi; An, Jin; Yang, Bao-Ping; La, Pei-Qing; Li, An, E-mail: lian2010@lut.cn

    2014-06-01

    A novel method for fabrication of superhydrophobic surfaces was developed by facile coating various metal oxide nanoparticles, including ZnO, Al{sub 2}O{sub 3} and Fe{sub 3}O{sub 4}, on various substrates followed by treatment with polydimethylsiloxane (PDMS) via chemical vapor deposition (CVD) method. Using ZnO nanoparticles as a model, the changes in the surface chemical composition and crystalline structures of the metal oxide nanoparticles by PDMS treatment were investigated by X-ray photoelectron spectroscopy (XPS), X-ray powder diffraction (XRD) and Fourier transform infrared (FTIR) analysis. The results show that the combination of the improved surface roughness generated from of the nanoparticles aggregation with the low surface-energy of silicon-coating originated from the thermal pyrolysis of PDMS would be responsible for the surface superhydrophobicity. By a simple dip-coating method, we show that the metal oxide nanoparticles can be easily coated onto the surfaces of various textural and dimensional substrates, including glass slide, paper, fabric or sponge, for preparation of superhydrophobic surfaces for different purpose. The present strategy may provide an inexpensive and new route to surperhydrophobic surfaces, which would be of technological significance for various practical applications especially for separation of oils or organic contaminates from water.

  20. Facile preparation of superhydrophobic surfaces based on metal oxide nanoparticles

    Science.gov (United States)

    Bao, Xue-Mei; Cui, Jin-Feng; Sun, Han-Xue; Liang, Wei-Dong; Zhu, Zhao-Qi; An, Jin; Yang, Bao-Ping; La, Pei-Qing; Li, An

    2014-06-01

    A novel method for fabrication of superhydrophobic surfaces was developed by facile coating various metal oxide nanoparticles, including ZnO, Al2O3 and Fe3O4, on various substrates followed by treatment with polydimethylsiloxane (PDMS) via chemical vapor deposition (CVD) method. Using ZnO nanoparticles as a model, the changes in the surface chemical composition and crystalline structures of the metal oxide nanoparticles by PDMS treatment were investigated by X-ray photoelectron spectroscopy (XPS), X-ray powder diffraction (XRD) and Fourier transform infrared (FTIR) analysis. The results show that the combination of the improved surface roughness generated from of the nanoparticles aggregation with the low surface-energy of silicon-coating originated from the thermal pyrolysis of PDMS would be responsible for the surface superhydrophobicity. By a simple dip-coating method, we show that the metal oxide nanoparticles can be easily coated onto the surfaces of various textural and dimensional substrates, including glass slide, paper, fabric or sponge, for preparation of superhydrophobic surfaces for different purpose. The present strategy may provide an inexpensive and new route to surperhydrophobic surfaces, which would be of technological significance for various practical applications especially for separation of oils or organic contaminates from water.

  1. AKD AND ASA MODEL SURFACES: PREPARATION AND CHARACTERIZATION

    Directory of Open Access Journals (Sweden)

    Janne Laine

    2007-11-01

    Full Text Available Model surfaces of alkyl ketene dimer (AKD and alkenyl succinic anhyd-ride (ASA were prepared by casting and spin-coating methods. The surface chemical composition and surface topography were investigated by XPS, ellipsometry, AFM and contact angle studies. Spin-coating resulted in layered structure of AKD and ASA surfaces; the molecular layer thickness of both AKD and ASA was found to be ca. 2.5 nm. To achieve a covering surface layer, an average thickness of ca. 35 nm was required. The rms roughness of the created surfaces was 1 - 6 nm. Colloidal probe adhesion measurements were performed to verify that the roughness was in a range suitable for these measurements. The high reactivity of ASA with water generated stability problems with the ASA layers and it has to be recognized that surface force measurements with ASA in aqueous environment are very difficult, if not impossible. How-ever, surfaces created in this way were found to be useful in providing explanations of earlier ASA adhesion studies. The contact angle measurements on ASA layers also indicated that it might be possible to asses the hydrolysis rate issues through a set of similar measurements.

  2. Roughness of surface of vacuum castings prepared in plaster moulds

    Directory of Open Access Journals (Sweden)

    M. Pawlak

    2011-07-01

    Full Text Available The results of researches on surface roughness of CuSn10 and CuSn5Zn5Pb5 bronzes and aluminum AlSi11 alloy vacuum castings prepared in plaster moulds are presented in this paper. Test samples were cut from stripe castings of dimensions 100x15x1 mm. Surfaces were carefully cleaned with use of soft brush than in ultrasonic washer and dried. Experimental castings were prepared in moulds made of two types of plaster. Cast temperatures were 1120 and 1200°C for bronzes and 700 and 800°C for silumin. Temperatures of the mould were 500 and 600°C for bronzes and 200 and 300°C for aluminum alloy. The roughness measurements were carried out with use of Hommelwerke Tester T1000. The average arithmetic deviation of roughness profile Ra, the ten-point height of irregularities Rz and maximum peak to valley height Rm, were measured.It can be stated, on the base of obtained results, that technology of casting in plaster moulds allows preparation of castings of very low roughness, average Ra=0,88÷1,74μm for bronzes and Ra=0,59÷0,83μm for aluminum alloys. Roughness of the surface depends in fact on the cast material. Type of plaster and casting parameters have negligible influence on it.

  3. Cr(VI) reduction in wastewater using a bimetallic galvanic reactor

    Energy Technology Data Exchange (ETDEWEB)

    Lugo-Lugo, Violeta [Centro Conjunto de Investigacion en Quimica Sustentable UAEM-UNAM, Universidad Autonoma del Estado de Mexico, Facultad de Quimica. Paseo Colon interseccion Paseo Tollocan S/N. C.P. 50120, Toluca (Mexico); Barrera-Diaz, Carlos, E-mail: cbarrera@uaemex.mx [Centro Conjunto de Investigacion en Quimica Sustentable UAEM-UNAM, Universidad Autonoma del Estado de Mexico, Facultad de Quimica. Paseo Colon interseccion Paseo Tollocan S/N. C.P. 50120, Toluca (Mexico); Bilyeu, Bryan [Xavier University of Louisiana, Department of Chemistry, 1 Drexel Drive, New Orleans, LA 70125 (United States); Balderas-Hernandez, Patricia [Centro Conjunto de Investigacion en Quimica Sustentable UAEM-UNAM, Universidad Autonoma del Estado de Mexico, Facultad de Quimica. Paseo Colon interseccion Paseo Tollocan S/N. C.P. 50120, Toluca (Mexico); Urena-Nunez, Fernando [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, Col. Escandon, Delegacion Miguel Hidalgo, C.P. 11801, Mexico, D.F. (Mexico); Sanchez-Mendieta, Victor [Centro Conjunto de Investigacion en Quimica Sustentable UAEM-UNAM, Universidad Autonoma del Estado de Mexico, Facultad de Quimica. Paseo Colon interseccion Paseo Tollocan S/N. C.P. 50120, Toluca (Mexico)

    2010-04-15

    The electrochemical reduction of Cr(VI)-Cr(III) in wastewater by iron and copper-iron bimetallic plates was evaluated and optimized. Iron has been used as a reducing agent, but in this work a copper-iron galvanic system in the form of bimetallic plates is applied to reducing hexavalent chromium. The optimal pH (2) and ratio of copper to iron surface areas (3.5:1) were determined in batch studies, achieving a 100% reduction in about 25 min. The Cr(VI) reduction kinetics for the bimetallic system fit a first order mechanism with a correlation of 0.9935. Thermodynamic analysis shows that the Cr(VI) reduction is possible at any pH value. However, at pH values above 3.0 for iron and 5.5 for chromium insoluble species appear, indicating that the reaction will be hindered. Continuous column studies indicate that the bimetallic copper-iron galvanic system has a reduction capacity of 9.5890 mg Cr(VI) cm{sup -2} iron, whereas iron alone only has a capacity of 0.1269 mg Cr(VI) cm{sup -2}. The bimetallic copper-iron galvanic system is much more effective in reducing hexavalent chromium than iron alone. The exhausted plates were analyzed by SEM, EDS, and XRD to determine the mechanism and the surface effects, especially surface fouling.

  4. Bimetallic Au-decorated Pd catalyst for the liquid phase hydrodechlorination of 2,4-dichlorophenol

    Science.gov (United States)

    Zhou, Juan; Chen, Huan; Chen, Quanyuan; Huang, Zhaolu

    2016-11-01

    Monometallic and bimetallic Pd-Au catalysts supported on multi-walled carbon nanotubes (CNTs) with varied Au cooperation amounts were prepared using the complexing-reduction method in the presence of tetrahydrofuran (THF). The liquid phase catalytic hydrodechlorination (HDC) of 2,4-dichlorophenol (2,4-DCP) was investigated over these bimetallic catalysts. The catalysts were characterized by N2 adsorption-desorption isotherms, X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, and H2 chemisorption. Characterization results showed that the co-reduction of Pd and Au mainly formed alloy-like structure. The bimetallic catalysts had smaller metal particles and larger numbers of exposed active site than that of monometallic catalysts. In addition, compared with Pd(1.7)/CNTs and Au(0.4)/CNTs, the binding energies of Pd 3d5/2 shifted to higher positions while that of Au 4f7/2 had negative shifts in the Pd-Au bimetallic catalysts, which can be ascribed to the electrons transferred from metal Pd to Au and the cationization of Pd particles was enhanced. Accordingly, the bimetallic Pd-Au particles with different Au contents in the catalysts exhibited varied synergistic effects for the catalytic HDC of 2,4-DCP, with Pd(1.8)Au(0.4)/CNTs having the highest catalytic activity. For the bimetallic catalysts, a disproportional increase of turnover frequency (TOF) was observed with increasing Au content due to the enhanced cationization of Pd particles. Moreover, the dechlorination of 2,4-DCP over the supported monometallic and bimetallic catalysts proceeded via both the stepwise and concerted pathway, and the concerted pathway became predominant with Au decoration amount in the catalyst.

  5. Efficiency of bimetallic PtPd on polydopamine modified on various carbon supports for alcohol oxidations

    Science.gov (United States)

    Pinithchaisakula, A.; Ounnunkad, K.; Themsirimongkon, S.; Promsawan, N.; Waenkaew, P.; Saipanya, S.

    2017-02-01

    In this work, the preparation, characterization, and electrocatalytic analysis of the catalysts on various carbon substrates for direct alcohol fuel cells were studied. Selected carbons were modified with/without polydopamine (labelled as PDA-C and C) and further metal electrodeposited incorporated onto the glassy carbon (labelled as 5Pt1Pd/PDA-C and 5Pt1Pd/C). Four various carbon materials were used e.g. graphite (G), carbon nanotube (CNT), graphene (GP) and graphene oxide (GO) and the carbons were modified with PDA denoted as PDA-G, PDA-CNT, PDA-GP and PDA-GO, respectively. The transmission electron microscopy (TEM) and scanning electron microscopy (SEM) experimental observation showed narrow size distribution of metal anchored on the PDA-C and C materials. Chemical compositions and oxidation states of the catalysts were determined by X-ray photoelectron spectroscopy (XPS) and energy-dispersive X-ray spectroscopy (EDX). The catalytic performances for small organic electro-oxidation (e.g. methanol and ethanol) were measured by cyclic voltammetry (CV). Among different PDA-C and C catalysts, monometallic Pt showed less activity than the bimetallic catalysts. Among catalysts with PDA, the 5Pt1Pd/PDA-GO catalyst facilitated methanol and ethanol oxidations with high oxidation currents and If/Ib value and stability with low potentials while among catalysts without PDA, the 5Pt1Pd/CNT provides highest activity and stability. It was found that the catalysts with PDA provided high activity and stability than the catalysts without PDA. The improved catalytic performance of the prepared catalysts could be related to the higher active surface area from polymer modification and bimetallic catalyst system in the catalyst composites.

  6. PREPARATION AND SURFACE PROPERTIES OF ACRYLIC COPOLYMERS CONTAINING FLUORINATED MONOMERS

    Institute of Scientific and Technical Information of China (English)

    Tai-jiang Gui; Hao Wei; Ying Zhao; Xiu-lin Wang; Du-jin Wang; Duan-fu Xu

    2006-01-01

    A series of copolymers comprising butylmethacrylate, styrene, butylacrylate, hydroxypropyl acrylate and perfluoroalkyl methacrylate were synthesized by the free radical polymerization using BPO as an initiator. The surface property of the copolymer films was subsequently characterized. The contact angle measurements and energy dispersive analysis of X-ray (EDAX) show that the length and content ofperfluoroalkyl side chains in the copolymers are crucial for the preparation of the film with low surface energy. At a given content of fluorinated monomers in the copolymers, the longer the perfluoroalkyl side chain, the larger the water contact angle of the copolymer films will be. On the other hand, the higher the content of fluorinated monomers, the lower the surface energy is. The water contact angle increases with the increase of the fluorinated monomer content and reaches a plateau at 3 wt% of fluorinated monomer content.

  7. Preparation of Bioactive Titanium Surfaces via Fluoride and Fibronectin Retention

    Directory of Open Access Journals (Sweden)

    Carlos Nelson Elias

    2012-01-01

    Full Text Available Statement of Problem. The chemical or topographic modification of the dental implant surface can affect bone healing, promote accelerated osteogenesis, and increase bone-implant contact and bonding strength. Objective. In this work, the effects of dental implant surface treatment and fibronectin adsorption on the adhesion of osteoblasts were analyzed. Materials and Methods. Two titanium dental implants (Porous-acid etching and PorousNano-acid etching followed by fluoride ion modification were characterized by high-resolution scanning electron microscopy, atomic force microscopy, and X-ray diffraction before and after the incorporation of human plasma fibronectin (FN. The objective was to investigate the biofunctionalization of these surfaces and examine their effects on the interaction with osteoblastic cells. Results. The evaluation techniques used showed that the Porous and PorousNano implants have similar microstructural characteristics. Spectrophotometry demonstrated similar levels of fibronectin adsorption on both surfaces (80%. The association indexes of osteoblastic cells in FN-treated samples were significantly higher than those in samples without FN. The radioactivity values associated with the same samples, expressed as counts per minute (cpm, suggested that FN incorporation is an important determinant of the in vitro cytocompatibility of the surfaces. Conclusion. The preparation of bioactive titanium surfaces via fluoride and FN retention proved to be a useful treatment to optimize and to accelerate the osseointegration process for dental implants.

  8. Synthesis and characteristics of Ag/Pt bimetallic nanocomposites by arc-discharge solution plasma processing.

    Science.gov (United States)

    Pootawang, Panuphong; Saito, Nagahiro; Takai, Osamu; Lee, Sang-Yul

    2012-10-05

    Arc discharge in solution, generated by applying a high voltage of unipolar pulsed dc to electrodes of Ag and Pt, was used as a method to form Ag/Pt bimetallic nanocomposites via electrode erosion by the effects of the electric arc at the cathode (Ag rod) and the sputtering at the anode (Pt rod). Ag/Pt bimetallic nanocomposites were formed as colloidal particles dispersed in solution via the reduction of hydrogen radicals generated during discharge without the addition of chemical precursor or reducing agent. At a discharge time of 30 s, the fine bimetallic nanoparticles with a mean particle size of approximately 5 nm were observed by transmission electron microscopy (TEM). With increasing discharge time, the bimetallic nanoparticle size tended to increase by forming an agglomeration. The presence of the relatively small amount of Pt dispersed in the Ag matrix could be observed by the analytical mapping mode of energy-dispersive x-ray spectroscopy and high-resolution TEM. This demonstrated that the synthesized particle was in the form of a nanocomposite. No contamination of other chemical substances was detected by x-ray photoelectron spectroscopy. Hence, solution plasma could be a clean and simple process to effectively synthesize Ag/Pt bimetallic nanocomposites and it is expected to be widely applicable in the preparation of several types of nanoparticle.

  9. Bimetallic nanoparticles for arsenic detection.

    Science.gov (United States)

    Moghimi, Nafiseh; Mohapatra, Mamata; Leung, Kam Tong

    2015-06-02

    Effective and sensitive monitoring of heavy metal ions, particularly arsenic, in drinking water is very important to risk management of public health. Arsenic is one of the most serious natural pollutants in soil and water in more than 70 countries in the world. The need for very sensitive sensors to detect ultralow amounts of arsenic has attracted great research interest. Here, bimetallic FePt, FeAu, FePd, and AuPt nanoparticles (NPs) are electrochemically deposited on the Si(100) substrate, and their electrochemical properties are studied for As(III) detection. We show that trace amounts of As(III) in neutral pH could be determined by using anodic stripping voltammetry. The synergistic effect of alloying with Fe leads to better performance for Fe-noble metal NPs (Au, Pt, and Pd) than pristine noble metal NPs (without Fe alloying). Limit of detection and linear range are obtained for FePt, FeAu, and FePd NPs. The best performance is found for FePt NPs with a limit of detection of 0.8 ppb and a sensitivity of 0.42 μA ppb(-1). The selectivity of the sensor has also been tested in the presence of a large amount of Cu(II), as the most detrimental interferer ion for As detection. The bimetallic NPs therefore promise to be an effective, high-performance electrochemical sensor for the detection of ultratrace quantities of arsenic.

  10. Preparation and Characterization of Plasma Cu Surface Modified Stainless Steel

    Institute of Scientific and Technical Information of China (English)

    ZHANG Xiangyu; TANG Bin; FAN Ailan; MA Yong; TIAN Linhai

    2012-01-01

    Cu modified layer was prepared on the surface of AISI304 stainless steel by plasma surface alloying technique.The effects of processing parameters on the thickness,surface topography,microstructure and chemical composition of Cu modified layer were characterized using glow discharge optical emission spectroscopy (GDOES),scanning electron microscopy (SEM) and X-ray diffraction (XRD).The experimental results show that the surface modified layer is a duplex layer (deposited + diffused layer) with thickness of about 26 μm under the optimum process parameters.The modified layer is mainly composed of a mixture of Cu and expanded austenite phase.The ball-on-disk results show that the modified layer possesses low friction coefficients (0.25) and excellent wear resistance (wear volume 0.005× 109 μm3).The Cu modified layer is very effective in killing the bacteria S.aureus.Meanwhile,no viable S.aureus is found after 3 h (100% killed) by contact with the Cu alloyed surface.

  11. Bimetallic gold-silver nanoplate array as a highly active SERS substrate for detection of streptavidin/biotin assemblies.

    Science.gov (United States)

    Bi, Liyan; Dong, Jian; Xie, Wei; Lu, Wenbo; Tong, Wei; Tao, Lin; Qian, Weiping

    2013-12-17

    The silver-modified gold nanoplate arrays as bimetallic surface-enhanced Raman scattering (SERS) substrates were optimized for the surface-enhanced Raman detection of streptavidin/biotin monolayer assemblies. The bimetallic gold-silver nanoplate arrays were fabricated by coating silver nanoparticles uniformly on the gold nanoplate arrays. Depending on silver nanoparticle coating, the localized surface plasmon resonance (LSPR) peak of the bimetallic gold-silver nanoplate arrays blue-shifted and broadened significantly. The common probe molecule, Niel Blue A sulfate (NBA) was used for testing the SERS activity of the bimetallic gold-silver nanoplate arrays. The SERS intensity increased with the silver nanoparticle coating, due to a large number of hot spots and nanoparticle interfaces. The platforms were tested against a monolayer of streptavidin functionalized over the bimetallic gold-silver nanoplate arrays showing that good quality spectra could be acquired with a short acquisition time. The supramolecular interaction between streptavidin (strep) and biotin showed subsequent modification of Raman spectra that implied a change of the secondary structure of the host biomolecule. And the detection concentration for biotin by this method was as low as 1.0 nM. The enhanced SERS performance of such bimetallic gold-silver nanoplate arrays could spur further interest in the integration of highly sensitive biosensors for rapid, nondestructive, and quantitative bioanalysis, particularly in microfluidics.

  12. Enhanced plasmonic behavior of bimetallic (Ag-Au multilayered spheres

    Directory of Open Access Journals (Sweden)

    Pal Umapada

    2011-01-01

    Full Text Available Abstract In this article we study the plasmonic behavior of some stable, highly biocompatible bimetallic metal-dielectric-metal (MDM and double concentric nanoshell (DCN structures. By simply switching the material of the inner structure from Au to Ag, the intensity of their surface plasmon resonance could be increased in the optical transparency region of the human tissues up to 20 and 60 percent for the MDM and DCN, respectively, while the biocompatibility is retained. The obtained results indicate that these novel structures could be highly suitable for surface enhanced Raman scattering and photothermal cancer therapy.

  13. A facile strategy to synthesize bimetallic Au/Ag nanocomposite film by layer-by-layer assembly technique

    Science.gov (United States)

    Zhang, Li; Wang, Cong; Zhang, Yi

    2012-05-01

    A facile strategy has been developed for the preparation of bimetallic gold-silver (Au-Ag) nanocomposite films by alternating absorption of poly-(ethyleneimine)-silver ions and Au onto substrates and subsequent reduction of the silver ions. The composition, micro-structure and properties of the {PEI-Ag/Au}n nanocomposite films were characterized by ultraviolet visible spectroscopy (UV-vis), transmisson electron microscopy (TEM), field emission scanning electron microscopy (FESEM), X-ray photoelectron spectroscopy (XPS), surface enhanced Raman scattering (SERS) and cyclic voltammetry (CV). The UV-vis characteristic absorbances of {PEI-Ag/Au}n nanocomposite thin film increase almost linear with the number of bilayers, which indicates a process of uniform assembling. Appearance of a double plasmon bands in the visible region and the lack of apparent core-shell structures in the TEM images confirm the formation of bimetallic Au-Ag nanoparticles. The result of XPS also demonstrates the existence of Ag and Au nanoparticles in the nanocomposite films. TEM and FESEM images show that these Ag and Au nanoparticles in the films possess sphere structure with the size of 20-25 nm. The resulting {PEI-Ag/Au}n films inherit the properties from both the metal Ag and Au, which exhibits a unique performance in SERS and electrocatalytic activities to the oxidation of dopamine. As a result, the {PEI-Ag/Au}n films are more attractive compared to {PEI-Ag/PSS}n and {PEI/Au}n films.

  14. Direct decomposition of methane over SBA-15 supported Ni, Co and Fe based bimetallic catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Pudukudy, Manoj, E-mail: manojpudukudy@gmail.com [Fuel Cell Institute, Universiti Kebangsaan Malaysia, UKM, Bangi 43600, Selangor (Malaysia); Department of Chemical and Process Engineering, Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia, UKM, Bangi 43600, Selangor (Malaysia); Yaakob, Zahira, E-mail: zahirayaakob65@gmail.com [Department of Chemical and Process Engineering, Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia, UKM, Bangi 43600, Selangor (Malaysia); Akmal, Zubair Shamsul [Department of Chemical and Process Engineering, Faculty of Engineering and Built Environment, Universiti Kebangsaan Malaysia, UKM, Bangi 43600, Selangor (Malaysia)

    2015-03-01

    Graphical abstract: - Highlights: • Synthesis and characterization of Ni, Co and Fe based bimetallic catalysts supported over SBA-15. • Thermocatalytic decomposition of methane over the SBA-15 supported bimetallic catalysts. • Enhanced catalytic efficiency of the bimetallic catalysts for the production of CO{sub x} free hydrogen and nanocarbon. • Production of value added open tip hollow multi-walled carbon nanotubes. • Crystalline characterization of carbon nanotubes by XRD, Raman and thermogravimetric analysis. - Abstract: Thermocatalytic decomposition of methane is an alternative route for the production of CO{sub x}-free hydrogen and carbon nanomaterials. In this work, a set of novel Ni, Co and Fe based bimetallic catalysts supported over mesoporous SBA-15 was synthesized by a facile wet impregnation route, characterized for their structural, textural and reduction properties and were successfully used for the methane decomposition. The fine dispersion of metal oxide particles on the surface of SBA-15, without affecting its mesoporous texture was clearly shown in the low angle X-ray diffraction patterns and the transmission electron microscopy (TEM) images. The nitrogen sorption analysis showed the reduced specific surface area and pore volume of SBA-15, after metal loading due to the partial filling of hexagonal mesopores by metal species. The results of methane decomposition experiments indicated that all of the bimetallic catalysts were highly active and stable for the reaction at 700 °C even after 300 min of time on stream (TOS). However, a maximum hydrogen yield of ∼56% was observed for the NiCo/SBA-15 catalyst within 30 min of TOS. A high catalytic stability was shown by the CoFe/SBA-15 catalyst with 51% of hydrogen yield during the course of reaction. The catalytic stability of the bimetallic catalysts was attributed to the formation of bimetallic alloys. Moreover, the deposited carbons were found to be in the form of a new set of hollow

  15. Laser deposition of bimetallic island films

    Science.gov (United States)

    Kucherik, A. O.; Arakelyan, S. M.; Kutrovskaya, S. V.; Osipov, A. V.; Istratov, A. V.; Vartanyan, T. A.; Itina, T. E.

    2016-08-01

    In this work the results of a bimetallic Au-Ag structure deposition from the colloidal system by nanosecond laser radiation are presented. The formation of the extended arrays of gold and silver nanoparticles with controlled morphology is examined. We report the results of formation bimetallic islands films with various electrical and optical properties. The changes in the optical properties of the obtained thin films are found to depend on their morphology.

  16. Enhanced dechlorination of trichloroethylene using electrospun polymer nanofibrous mats immobilized with iron/palladium bimetallic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Hui [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai 201620 (China); College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620 (China); Huang, Yunpeng; Shen, Mingwu; Guo, Rui; Cao, Xueyan [College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620 (China); Shi, Xiangyang, E-mail: xshi@dhu.edu.cn [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai 201620 (China); College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai 201620 (China); CQM - Centro de Quimica da Madeira, Universidade da Madeira, Campus da Penteada, 9000-390 Funchal (Portugal)

    2012-04-15

    Fe/Pd bimetallic nanoparticles (NPs) have held great promise for treating trichloroethylene (TCE)-contaminated groundwater, without the accumulation of chlorinated intermediates. However, the conventionally used colloidal Fe/Pd NPs usually aggregate rapidly, resulting in a reduced reactivity. To reduce the particle aggregation, we employed electrospun polyacrylic acid (PAA)/polyvinyl alcohol (PVA) polymer nanofibers as a nanoreactor to immobilize Fe/Pd bimetallic NPs. In the study, the water-stable PAA/PVA nanofibrous mats were complexed with Fe (III) ions via the binding with the free carboxyl groups of PAA for subsequent formation and immobilization of zero-valent iron (ZVI) NPs. Fe/Pd bimetallic NPs were then formed by the partial reduction of Pd(II) ions with ZVI NPs. The formed electrospun nanofibrous mats containing Fe/Pd bimetallic NPs with a diameter of 2.8 nm were characterized by scanning electron microscopy, energy-dispersive spectroscopy, transmission electron microscopy, thermogravimetric analysis, and inductively coupled plasma-atomic emission spectroscopy. The Fe/Pd NP-containing electrospun PAA/PVA nanofibrous mats exhibited higher reactivity than that of the ZVI NP-containing mats or colloidal Fe/Pd NPs in the dechlorination of trichloroethylene (TCE), which was used as a model contaminant. With the high surface area to volume ratio, high porosity, and great reusability of the fibrous mats immobilized with the bimetallic NPs, the composite nanofibrous mats should be amenable for applications in remediation of various environmental contaminants.

  17. Classical dynamics simulations of directional effects in sputtering from a bimetallic surface: c(2x2)-Pb/Cu(1 0 0)

    Energy Technology Data Exchange (ETDEWEB)

    Karolewski, M.A. E-mail: mkarol@ualberta.ca

    2002-07-01

    Classical dynamics sputtering simulations have been performed for a c(2x2)-Pb/Cu(1 0 0) target. The primary projectile was 3 keV Ar. The simulation model employs classical many-body tight-binding potentials to describe the bonding interactions between Pb and Cu atoms. Simulations were carried out for projectiles incident in the <0 1 1> and <0 1 0> azimuthal directions, with altitudinal angles (phi (cursive,open) Greek{sub i}) in the range 10-90 deg. The simulation results have been discussed with a view to understanding the sputtering characteristics of heavy metal overlayer systems and the information content of their surface mass spectra. Attention has been given to the following issues: (a) the enhancement of surface layer sputtering at grazing projectile incidence, (b) the angular distributions of sputtered atoms and (c) the prospects for surface structure determination by shadow cone enhanced sputtering. The yields of dimer and trimer cluster species sputtered from Pb/Cu(1 0 0) are also reported. For phi (cursive,open) Greek{sub i}=90 deg., the sputter yields (Y) of Pb and Cu are estimated to be 3.60{+-}0.1 and 2.56{+-}0.1, respectively. The sputter yields of Pb and Cu are predicted to display a strong dependence on the projectile altitudinal angle of incidence, phi (cursive,open) Greek, due to projectile channelling effects. However, variations in the projectile direction of incidence are found to modify the total sputter yields of Pb and Cu atoms in constant proportion, except near grazing incidence (phi (cursive,open) Greek{sub i}<25 deg. ), when an increase in the ratio of sputter yields Y(Pb)/Y(Cu) is predicted. The angular distributions of sputtered atoms are found to have similar characteristics to those reported for other metallic surfaces with (1 0 0) face-centred cubic (fcc) surface structures. The peak positions in these distributions are determined by the placement of the atoms which coordinate the lattice sites of origin of the sputtered atoms. It

  18. Bimetallic Metal-Organic Frameworks for Controlled Catalytic Graphitization of Nanoporous Carbons

    Science.gov (United States)

    Tang, Jing; Salunkhe, Rahul R.; Zhang, Huabin; Malgras, Victor; Ahamad, Tansir; Alshehri, Saad M.; Kobayashi, Naoya; Tominaka, Satoshi; Ide, Yusuke; Kim, Jung Ho; Yamauchi, Yusuke

    2016-07-01

    Single metal-organic frameworks (MOFs), constructed from the coordination between one-fold metal ions and organic linkers, show limited functionalities when used as precursors for nanoporous carbon materials. Herein, we propose to merge the advantages of zinc and cobalt metals ions into one single MOF crystal (i.e., bimetallic MOFs). The organic linkers that coordinate with cobalt ions tend to yield graphitic carbons after carbonization, unlike those bridging with zinc ions, due to the controlled catalytic graphitization by the cobalt nanoparticles. In this work, we demonstrate a feasible method to achieve nanoporous carbon materials with tailored properties, including specific surface area, pore size distribution, degree of graphitization, and content of heteroatoms. The bimetallic-MOF-derived nanoporous carbon are systematically characterized, highlighting the importance of precisely controlling the properties of the carbon materials. This can be done by finely tuning the components in the bimetallic MOF precursors, and thus designing optimal carbon materials for specific applications.

  19. A general approach for the synthesis of bimetallic M–Sn (M = Ru, Rh and Ir) catalysts for efficient hydrogenolysis of ester

    KAUST Repository

    Samal, Akshaya K.

    2016-11-24

    A versatile synthetic method was applied for the preparation of Sn containing bimetallic catalysts. The synthesis was performed by simply mixing the super hydride [LiB(C2H5)(3)H], with a metal (Ru, Rh or Ir) salt and an organotin complex in tetrahydrofuran solvent without using any surfactant. This leads to the formation of monodispersed M-Sn (M = Ru, Rh or Ir) bimetallic nanoparticles (NPs). These bimetallic catalysts show high performances in the hydrogenolysis of ester to the corresponding alcohol.

  20. Enhancement of bimetallic Fe-Mn/CNTs nano catalyst activity and product selectivity using microemulsion technique

    Institute of Scientific and Technical Information of China (English)

    Zahra; Zolfaghari; Ahmad; Tavasoli; Saber; Tabyar; Ali; Nakhaei; Pour

    2014-01-01

    Bimetallic Fe-Mn nano catalysts supported on carbon nanotubes(CNTs) were prepared using microemulsion technique with water-to-surfactant ratios of 0.4-1.6. The nano catalysts were extensively characterized by different methods and their activity and selectivity in Fischer-Tropsch synthesis(FTS) have been assessed in a fixed-bed microreactor. The physicochemical properties and performance of the nanocatalysts were compared with the catalyst prepared by impregnation method. Very narrow particle size distribution has been produced by the microemulsion technique at relatively high loading of active metal. TEM images showed that small metal nano particles in the range of 3–7 nm were not only confined inside the CNTs but also located on the outer surface of the CNTs. Using microemulsion technique with water to surfactant ratio of0.4 decreased the average iron particle sizes to 5.1 nm. The reduction percentage and dispersion percentage were almost doubled. Activity and selectivity were found to be dependent on the catalyst preparation method and average iron particle size. CO conversion and FTS rate increased from 49.1% to 71.0% and 0.144 to 0.289 gHC/(gcat h), respectively. While the WGS rate decreased from 0.097 to 0.056 gCO2/(gcat h). C5+liquid hydrocarbons selectivity decreased slightly and olefins selectivity almost doubled.

  1. Nanocrystalline MgO supported nickel-based bimetallic catalysts for carbon dioxide reforming of methane

    Energy Technology Data Exchange (ETDEWEB)

    Meshkani, Fereshteh [Catalyst and Advanced Materials Research Laboratory, Chemical Engineering Department, Faculty of Engineering, University of Kashan, Kashan (Iran); Rezaei, Mehran [Catalyst and Advanced Materials Research Laboratory, Chemical Engineering Department, Faculty of Engineering, University of Kashan, Kashan (Iran); Institute of Nanoscience and Nanotechnology, University of Kashan, Kashan (Iran)

    2010-10-15

    Nanocrystalline magnesium oxide with high surface area and plate-like shape was employed as catalyst support for preparation of nickel-based bimetallic catalysts in methane reforming with carbon dioxide. The prepared samples were characterized by X-ray diffraction (XRD), N{sub 2} adsorption (BET), Temperature programmed oxidation and desorption (TPO-TPD), Thermal gravimetric and differential thermal gravimetric (TGA-DTG), H{sub 2} chemisorption and Transmission and electron microscopies (TEM and SEM) analyses. CO{sub 2}-TPD data showed the high CO{sub 2} adsorption capacity of catalysts which improves the resistance of catalysts against the carbon formation. The H{sub 2} chemisorption results also indicated that the addition of Pt to nickel catalyst improved the nickel dispersion. The obtained results revealed that the prepared catalysts showed a high activity and stability during the reaction with a low amount of deposited carbon. Addition of Pt to nickel catalyst improved both the activity and resistivity against carbon formation. (author)

  2. Atomic Structure of Au−Pd Bimetallic Alloyed Nanoparticles

    KAUST Repository

    Ding, Yong

    2010-09-08

    Using a two-step seed-mediated growth method, we synthesized bimetallic nanoparticles (NPs) having a gold octahedron core and a palladium epitaxial shell with controlled Pd-shell thickness. The mismatch-release mechanism between the Au core and Pd shell of the NPs was systematically investigated by high-resolution transmission electron microscopy. In the NPs coated with a single atomic layer of Pd, the strain between the surface Pd layer and the Au core is released by Shockley partial dislocations (SPDs) accompanied by the formation of stacking faults. For NPs coated with more Pd (>2 nm), the stacking faults still exist, but no SPDs are found. This may be due to the diffusion of Au atoms into the Pd shell layers to eliminate the SPDs. At the same time, a long-range ordered L11 AuPd alloy phase has been identified in the interface area, supporting the assumption of the diffusion of Au into Pd to release the interface mismatch. With increasing numbers of Pd shell layers, the shape of the Au-Pd NP changes, step by step, from truncated-octahedral to cubic. After the bimetallic NPs were annealed at 523 K for 10 min, the SPDs at the surface of the NPs coated with a single atomic layer of Pd disappeared due to diffusion of the Au atoms into the surface layer, while the stacking faults and the L11 Au-Pd alloyed structure remained. When the annealing temperature was increased to 800 K, electron diffraction patterns and diffraction contrast images revealed that the NPs became a uniform Au-Pd alloy, and most of the stacking faults disappeared as a result of the annealing. Even so, some clues still support the existence of the L11 phase, which suggests that the L11 phase is a stable, long-range ordered structure in Au-Pd bimetallic NPs. © 2010 American Chemical Society.

  3. Direct decomposition of methane over SBA-15 supported Ni, Co and Fe based bimetallic catalysts

    Science.gov (United States)

    Pudukudy, Manoj; Yaakob, Zahira; Akmal, Zubair Shamsul

    2015-03-01

    Thermocatalytic decomposition of methane is an alternative route for the production of COx-free hydrogen and carbon nanomaterials. In this work, a set of novel Ni, Co and Fe based bimetallic catalysts supported over mesoporous SBA-15 was synthesized by a facile wet impregnation route, characterized for their structural, textural and reduction properties and were successfully used for the methane decomposition. The fine dispersion of metal oxide particles on the surface of SBA-15, without affecting its mesoporous texture was clearly shown in the low angle X-ray diffraction patterns and the transmission electron microscopy (TEM) images. The nitrogen sorption analysis showed the reduced specific surface area and pore volume of SBA-15, after metal loading due to the partial filling of hexagonal mesopores by metal species. The results of methane decomposition experiments indicated that all of the bimetallic catalysts were highly active and stable for the reaction at 700 °C even after 300 min of time on stream (TOS). However, a maximum hydrogen yield of ∼56% was observed for the NiCo/SBA-15 catalyst within 30 min of TOS. A high catalytic stability was shown by the CoFe/SBA-15 catalyst with 51% of hydrogen yield during the course of reaction. The catalytic stability of the bimetallic catalysts was attributed to the formation of bimetallic alloys. Moreover, the deposited carbons were found to be in the form of a new set of hollow multi-walled nanotubes with open tips, indicating a base growth mechanism, which confirm the selectivity of SBA-15 supported bimetallic catalysts for the formation of open tip carbon nanotubes. The Raman spectroscopic and thermogravimetric analysis of the deposited carbon nanotubes over the bimetallic catalysts indicated their higher graphitization degree and oxidation stability.

  4. The effect of metal cluster deposition route on structure and photocatalytic activity of mono- and bimetallic nanoparticles supported on TiO2 by radiolytic method

    Science.gov (United States)

    Klein, Marek; Nadolna, Joanna; Gołąbiewska, Anna; Mazierski, Paweł; Klimczuk, Tomasz; Remita, Hynd; Zaleska-Medynska, Adriana

    2016-08-01

    TiO2 (P25) was modified with small and relatively monodisperse mono- and bimetallic clusters (Ag, Pd, Pt, Ag/Pd, Ag/Pt and Pd/Pt) induced by radiolysis to improve its photocatalytic activity. The as-prepared samples were characterized by X-ray fluorescence spectrometry (XRF), photoluminescence spectrometry (PL), diffuse reflectance spectroscopy (DRS), X-ray powder diffractometry (XRD), scanning transition electron microscopy (STEM) and BET surface area analysis. The effect of metal type (mono- and bimetallic modification) as well as deposition method (simultaneous or subsequent deposition of two metals) on the photocatalytic activity in toluene removal in gas phase under UV-vis irradiation (light-emitting diodes- LEDs) and phenol degradation in liquid phase under visible light irradiation (λ > 420 nm) were investigated. The highest photoactivity under Vis light was observed for TiO2 co-loaded with platinum (0.1%) and palladium (0.1%) clusters. Simultaneous addition of metal precursors results in formation of larger metal nanoparticles (15-30 nm) on TiO2 surface and enhances the Vis-induced activity of Ag/Pd-TiO2 up to four times, while the subsequent metal ions addition results in formation of metal particle size ranging from 4 to 20 nm. Subsequent addition of metal precursors results in formation of BNPs (bimetallic nanoparticle) composites showing higher stability in four cycles of toluene degradation under UV-vis. Obtained results indicated that direct electron transfer from the BNPs to the conduction band of the semiconductor is responsible for visible light photoactivity, whereas superoxide radicals (such as O2rad- and rad OOH) are responsible for pollutants degradation over metal-TiO2 composites.

  5. Optical properties and sensing applications of stellated and bimetallic nanoparticles

    Science.gov (United States)

    Smith, Alison F.

    This dissertation focuses on developing guidelines to aid in the design of new bimetallic platforms for sensing applications. Stellated metal nanostructures are a class of plasmonic colloids in which large electric field enhancements can occur at sharp features, making them excellent candidates for surface enhanced Raman spectroscopy (SERS) and surface enhanced infrared spectroscopy (SE-IRS) platforms. Shape-dependent rules for convex polyhedra such as cubes or octahedra exist, which describe far-field scattering and near-field enhancements. However, such rules are lacking for their concave (stellated) counterparts. This dissertation presents the optical response of stellated Au nanocrystals with Oh, D4h, D3h, C2v, and T d symmetry, which were modeled to systematically investigate the role of symmetry, branching, and particle orientation with respect to excitation source using finite difference time domain (FDTD) calculations. Expanding on stellated nanostructures, bimetallic compositions introduce an interplay between overall architecture and composition to provide tunable optical properties and the potential of new functionality. However, decoupling the complex compositional and structural contributions to the localized surface plasmon resonance (LSPR) remains a challenge, especially when the monometallic counterparts are not synthetically accessible for comparison and the theoretical tools for capturing gradient compositions are lacking. This dissertation explores a stellated Au-Pd nanocrystal model system with Oh symmetry to decouple structural and complex compositional effects on LSPR. (Abstract shortened by ProQuest.).

  6. Enantioselective Epoxide Polymerization Using a Bimetallic Cobalt Catalyst

    KAUST Repository

    Thomas, Renee M.

    2010-11-24

    A highly active enantiopure bimetallic cobalt complex was explored for the enantioselective polymerization of a variety of monosubstituted epoxides. The polymerizations were optimized for high rates and stereoselectivity, with s-factors (kfast/kslow) for most epoxides exceeding 50 and some exceeding 300, well above the threshold for preparative utility of enantiopure epoxides and isotactic polyethers. Values for mm triads of the resulting polymers are typically greater than 95%, with some even surpassing 98%. In addition, the use of a racemic catalyst allowed the preparation of isotactic polyethers in quantitative yields. The thermal properties of these isotactic polyethers are presented, with many polymers exhibiting high T m values. This is the first report of the rapid synthesis of a broad range of highly isotactic polyethers via the enantioselective polymerization of racemic epoxides. © 2010 American Chemical Society.

  7. Porous bimetallic PdNi catalyst with high electrocatalytic activity for ethanol electrooxidation.

    Science.gov (United States)

    Feng, Yue; Bin, Duan; Yan, Bo; Du, Yukou; Majima, Tetsuro; Zhou, Weiqiang

    2017-05-01

    Porous bimetallic PdNi catalysts were fabricated by a novel method, namely, reduction of Pd and Ni oxides prepared via calcining the complex chelate of PdNi-dimethylglyoxime (PdNi-dmg). The morphology and composition of the as-prepared PdNi were investigated by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). Furthermore, the electrochemical properties of PdNi catalysts towards ethanol electrooxidation were also studied by electrochemical impedance spectrometry (EIS), cyclic voltammetry (CV) and chronoamperometry (CA) measurement. In comparison with porous Pd and commercial Pd/C catalysts, porous structural PdNi catalysts showed higher electrocatalytic activity and durability for ethanol electrooxidation, which may be ascribed to Pd and Ni property, large electroactive surface area and high electron transfer property. The Ni exist in the catalyst in the form of the nickel hydroxides (Ni(OH)2 and NiOOH) which have a high electron and proton conductivity enhances the catalytic activity of the catalysts. All results highlight the great potential application of the calcination-reduction method for synthesizing high active porous PdNi catalysts in direct ethanol fuel cells.

  8. Preparation of a PTE simulacrum based on surface molecular imprinting

    Institute of Scientific and Technical Information of China (English)

    Yong Guo; Ying Yang; Tian Ying Guo

    2011-01-01

    Firstly, we synthesized N-methacryloyl-histidine monomer and N-methacryIoyl-histidine-Cu2+ complex (MAH-Cu2+). Then the molecular imprinting polymers (MIP) has been prepared by surface grafting on uniform polystyrene (PS) core using reversible addition-fragmentation transfer polymerization (RAFT) with MAH-Cu2+ as the functional monomer, methyl paraoxon as the template to simulate phosphotriesterase (PTE). Finally, we have investigated the catalytic hydrolytic activities of MIP and non-imprinting polymers (NIP) to the template methyl paraoxon and the template analogue ethyl paraoxon respectively by UV spectrophotometry. The results showed that the catalytic hydrolytic activity of MIP to the template methyl paraoxon was highest and the value of k is 8.67 × 105 mmol L-1 min-1 3.89-fold higher than MIP to the template analogue ethyl paraoxon, 2.79-fold higher than NIP to the template methyl paraoxon. The KM, rm of MIP are also determined, and Km = 3.95 × 10-4 mol/L, rm = 2.12 μmol/ min. The MIP can be reused with only lose 7% of catalytic activity for four cycles.

  9. Bioactive carbon-PEEK composites prepared by chemical surface treatment.

    Science.gov (United States)

    Miyazaki, Toshiki; Matsunami, Chisato; Shirosaki, Yuki

    2017-01-01

    Polyetheretherketone (PEEK) has attracted much attention as an artificial intervertebral spacer for spinal reconstruction. Furthermore, PEEK plastic reinforced with carbon fiber has twice the bending strength of pure PEEK. However, the PEEK-based materials do not show ability for direct bone bonding, i.e., bioactivity. Although several trials have been conducted for enabling PEEK with bioactivity, few studies have reported on bioactive surface modification of carbon-PEEK composites. In the present study, we attempted the preparation of bioactive carbon-PEEK composites by chemical treatments with H2SO4 and CaCl2. Bioactivity was evaluated by in vitro apatite formation in simulated body fluid (SBF). The apatite formation on the carbon-PEEK composite was compared with that of pure PEEK. Both pure PEEK and carbon-PEEK composite formed the apatite in SBF when they were treated with H2SO4 and CaCl2; the latter showed higher apatite-forming ability than the former. It is conjectured that many functional groups able to induce the apatite nucleation, such as sulfo and carboxyl groups, are incorporated into the dispersed carbon phase in the carbon-PEEK composites.

  10. Microwave-assisted synthesis and characterization of bimetallic PtRu alloy nanoparticles supported on carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Rahsepar, Mansour, E-mail: rahsepar@shirazu.ac.ir [Department of Materials Science and Engineering, School of Engineering, Shiraz University, Zand Boulevard, Shiraz, 7134851154 (Iran, Islamic Republic of); Kim, Hasuck, E-mail: hasuckim@snu.ac.kr [Department of Chemistry, Seoul National University, 599 Gwanak-ro, Gwanak-gu, Seoul, 151-747 (Korea, Republic of); Department of Energy Systems Engineering, Daegu Gyeongbuk Institute of Science & Technology, Daegu, 711-873 (Korea, Republic of)

    2015-11-15

    Multiwalled carbon nanotube (MWCNT) supported PtRu nanoparticles were synthesized by using a microwave-assisted improved impregnation technique. X-ray diffraction, transmission electron microscopy and X-ray photo electron spectroscopy were used to characterize the prepared PtRu/MWCNT nanoparticles. The PtRu nanoparticles with a satisfactory dispersion were formed on the external surface of MWCNTs. The CO stripping experiment was performed to evaluate the poisoning resistance of the prepared PtRu/MWCNT nanoparticles. Results of electrochemical measurements indicate that the prepared PtRu/MWCNTs shows an enhanced performance toward CO poisoning. The results of characterization revealed that microwave-assisted improved impregnation technique have a high yield of alloy phase formation and could be effectively used as a simple, quick and efficient technique for preparation of bimetallic PtRu/MWCNT nanoparticles. - Highlights: • Highly dispersed PtRu/MWCNTs were formed without use of any stabilizing agent. • Microwave irradiation enhances the uniform dispersion of the PtRu nanoparticles. • Microwave-assisted improved impregnation have a high yield of alloy phase formation. • The prepared PtRu/MWCNTs shows an enhanced performance toward CO poisoning.

  11. Structures of small Pd Pt bimetallic clusters by Monte Carlo simulation

    Science.gov (United States)

    Cheng, Daojian; Huang, Shiping; Wang, Wenchuan

    2006-11-01

    Segregation phenomena of Pd-Pt bimetallic clusters with icosahedral and decahedral structures are investigated by using Monte Carlo method based on the second-moment approximation of the tight-binding (TB-SMA) potentials. The simulation results indicate that the Pd atoms generally lie on the surface of the smaller clusters. The three-shell onion-like structures are observed in 55-atom Pd-Pt bimetallic clusters, in which a single Pd atom is located in the center, and the Pt atoms are in the middle shell, while the Pd atoms are enriched on the surface. With the increase of Pd mole fraction in 55-atom Pd-Pt bimetallic clusters, the Pd atoms occupy the vertices of clusters first, then edge and center sites, and finally the interior shell. It is noticed that some decahedral structures can be transformed into the icosahedron-like structure at 300 and 500 K. Comparisons are made with previous experiments and theoretical studies of Pd-Pt bimetallic clusters.

  12. Bimetallic Catalysts Containing Gold and Palladium for Environmentally Important Reactions

    Directory of Open Access Journals (Sweden)

    Ahmad Alshammari

    2016-07-01

    Full Text Available Supported bimetallic nanoparticles (SBN are extensively used as efficient redox catalysts. This kind of catalysis particularly using SBN has attracted immense research interest compared to their parent metals due to their unique physico-chemical properties. The primary objective of this contribution is to provide comprehensive overview about SBN and their application as promising catalysts. The present review contains four sections in total. Section 1 starts with a general introduction, recent progress, and brief summary of the application of SBN as promising catalysts for different applications. Section 2 reviews the preparation and characterization methods of SBN for a wide range of catalytic reactions. Section 3 concentrates on our own results related to the application of SBN in heterogeneous catalysis. In this section, the oxidation of cyclohexane to adipic acid (an eco-friendly and novel approach will be discussed. In addition, the application of bimetallic Pd catalysts for vapor phase toluene acetoxylation in a fixed bed reactor will also be highlighted. Acetoxylation of toluene to benzyl acetate is another green route to synthesize benzyl acetate in one step. Finally, Section 4 describes the summary of the main points and also presents an outlook on the application of SBN as promising catalysts for the production of valuable products.

  13. Improved catalytic activity of laser generated bimetallic and trimetallic nanoparticles.

    Science.gov (United States)

    Singh, Rina; Soni, R K

    2014-09-01

    We report synthesis of silver nanoparticles, bimetallic (Al2O3@Ag) nanoparticles and trimetallic (Al2O3@AgAu) nanoparticles by nanosecond pulse laser ablation (PLA) in deionized water. Two-step laser ablation methodologies were adopted for the synthesis of bi- and tri-metallic nanoparticles. In this method a silver or gold target was ablated in colloidal solution of γ-alumina nanoparticles prepared by PLA. The TEM image analysis of bimetallic and trimetallic particles reveals deposition of fine silver particles and Ag-Au alloy particles, respectively, on large alumina particles. The laser generated nanoparticles were tested for catalytic reduction of 4-nitrophenol to 4-aminophenol and showed excellent catalytic behaviour. The catalytic rate was greatly improved by incorporation of additional metal in silver nanoparticles. The catalytic efficiency of trimetallic Al2O3@AgAu for reduction of 4-nitrophenol to 4-aminophenol was remarkably enhanced and the catalytic reaction was completed in just 5 sec. Even at very low concentration, both Al2O3@Ag nanoparticles and Al2O3@AgAu nanoparticles showed improved rate of catalytic reduction than monometallic silver nanoparticles. Our results demonstrate that alumina particles in the solution not only provide the active sites for particle dispersion but also improve the catalytic activity.

  14. CO2 activation on bimetallic CuNi nanoparticles☆

    Institute of Scientific and Technical Information of China (English)

    Natalie Austin; Brandon Butina; Giannis Mpourmpakis⁎

    2016-01-01

    Density functional theory calculations have been performed to investigate the structural, electronic, and CO2 adsorption properties of 55-atom bimetallic CuNi nanoparticles (NPs) in core-shell and decorated architectures, as well as of their monometallic counterparts. Our results revealed that with respect to the monometallic Cu55 and Ni55 parents, the formation of decorated Cu12Ni43 and core-shell Cu42Ni13 are energetically favorable. We found that CO2 chemisorbs on monometallic Ni55, core-shell Cu13Ni42, and decorated Cu12Ni43 and Cu43Ni12, whereas, it physisorbs on monometallic Cu55 and core-shell Cu42Ni13. The presence of surface Ni on the NPs is key in strongly adsorbing and activating the CO2 molecule (linear to bent transition and elongation of C˭O bonds). This activation occurs through a charge transfer from the NPs to the CO2 molecule, where the local metal d-orbital density localization on surface Ni plays a pivotal role. This work identifies insightful structure-property relationships for CO2 activation and highlights the importance of keeping a balance between NP stability and CO2 adsorption behavior in designing catalytic bimetallic NPs that activate CO2.

  15. CO2 activation on bimetallic CuNi nanoparticles

    Directory of Open Access Journals (Sweden)

    Natalie Austin

    2016-10-01

    Full Text Available Density functional theory calculations have been performed to investigate the structural, electronic, and CO2 adsorption properties of 55-atom bimetallic CuNi nanoparticles (NPs in core-shell and decorated architectures, as well as of their monometallic counterparts. Our results revealed that with respect to the monometallic Cu55 and Ni55 parents, the formation of decorated Cu12Ni43 and core-shell Cu42Ni13 are energetically favorable. We found that CO2 chemisorbs on monometallic Ni55, core-shell Cu13Ni42, and decorated Cu12Ni43 and Cu43Ni12, whereas, it physisorbs on monometallic Cu55 and core-shell Cu42Ni13. The presence of surface Ni on the NPs is key in strongly adsorbing and activating the CO2 molecule (linear to bent transition and elongation of C˭O bonds. This activation occurs through a charge transfer from the NPs to the CO2 molecule, where the local metal d-orbital density localization on surface Ni plays a pivotal role. This work identifies insightful structure-property relationships for CO2 activation and highlights the importance of keeping a balance between NP stability and CO2 adsorption behavior in designing catalytic bimetallic NPs that activate CO2.

  16. Monometallic Pd and Pt and Bimetallic Pd-Pt/Al2O3-TiO2 for the HDS of DBT: Effect of the Pd and Pt Incorporation Method

    Directory of Open Access Journals (Sweden)

    Reynaldo Martínez Guerrero

    2014-01-01

    Full Text Available The effect of the preparation method of monometallic Pd and Pt and bimetallic Pd-Pt/Al2O3-TiO2 catalysts on the hydrodesulfurization (HDS of dibenzothiophene (DBT was investigated in this study. The synthesis was accomplished using three methods: (A impregnation, (B metal organic chemical vapor deposition (MOCVD, and (C impregnation-MOCVD. The bimetallic Pd-Pt catalyst prepared by the impregnation-MOCVD method was most active for the HDS of DBT compared to those prepared by the single impregnation or MOCVD method due to the synergetic effect between both noble metals. The greater selectivity toward biphenyl indicated that this bimetallic Pd-Pt catalyst preferentially removes sulfur via the direct desulfurization mechanism. However, the bimetallic Pd-Pt catalyst prepared using the single MOCVD method did not produce any cyclohexylbenzene, which is most likely associated with the hydrogenation/dehydrogenation sites.

  17. 核-壳结构双金属纳米颗粒的表面增强拉曼散射的理论研究%Theoretical study of surface enhanced Raman scattering from core-shell bimetallic nanoparticle

    Institute of Scientific and Technical Information of China (English)

    陈李清; 殷一丁

    2012-01-01

    在准静态极限下,首先通过第一性原理推导带壳纳米颗粒的多重极化率,然后运用GN模型研究Ag-Au核-壳结构双金属纳米颗粒的表面增强拉曼散射.研究结果表明,随着Au壳层厚度的增加,短波长处SPR峰发生红移现象,强度减小,而长波长处的SPR峰红移的过程中伴随着强度的增加.%In this paper, we present a first-principles approach to the study of the multipolar moments induced by the coated bimetallic particles in the quasi-static limit. Based on the semiclassi-cal Gersten-Nitzan model, we take one step forward to investigate the the enhancement radio ( R) from bimetallic interface in Ag-Au core-shell structure nanoshell. Numerical results show that the longer wavelength peak red shifts slightly and gets intense, while the shorter wavelength peak red shifts nonlinearly and decreases in intensity with increasing the Au shell thickness.

  18. Study of Pd-Sn/Al{sub 2}O{sub 3} catalysts prepared by an oxide colloidal route; Etude de catalyseurs Pd-Sn/Al{sub 2}O{sub 3} prepares par voie colloidale oxyde

    Energy Technology Data Exchange (ETDEWEB)

    Verdier, St.

    2001-09-01

    The oxide colloidal route, developed in the laboratory for mono-metallic catalysts, consists in preparing a metallic oxide hydro-sol which leads to the supported catalyst after deposition onto a support and an activation stage. In this work, this method has been adapted to the preparation of alumina supported bimetallic Pd-Sn catalysts to determine its interest for the control of the properties of the bimetallic phase (size, composition and structure). In the preliminary study concerning tin oxide sols, SnO{sub 2} (size=2,3 nm) and Sn{sub 6}O{sub 4}(OH){sub 4} (size = 25 nm) nano-particles were synthesized by neutralization respectively for tin(IV) and tin(H). The control through the pH of the aggregation of the PdO and SnO{sub 2} particles revealed that increasing oxide solubility promotes integral re-dispersion of the oxide particles. To synthesize oxide bimetallic sols, three strategies were defined. Copolymerization (formation of a mixed oxide nano-sol by cross condensation of both metals) does not lead to a mixed oxide Pd-Sn phase. Surface precipitation (neutralization of the second metal in the presence of the first oxide sol) yields nano-particles of both oxides in close interaction. Adsorption (adsorption of the second metal onto the first oxide sol) significantly occurs when contacting tin with a basic PdO sol (hydrolytic adsorption). The characterization and the assessment of the catalytic properties (selective hydrogenation of buta-1,3-diene) of the catalysts prepared by deposition of oxide bimetallic sols showed that the oxide colloidal route allows the control of the properties of the supported bimetallic phase. Moreover, our results display that both Pd-Sn alloy formation and,aggregation of the metallic particles contribute to increase the selectivity for this reaction. (author)

  19. Porous Diatomite-Immobilized Cu–Ni Bimetallic Nanocatalysts for Direct Synthesis of Dimethyl Carbonate

    Directory of Open Access Journals (Sweden)

    Yong Chen

    2012-01-01

    Full Text Available A series of diatomite-immobilized Cu–Ni bimetallic nanocatalysts was prepared under ultrasonication and evaluated for the direct synthesis of dimethyl carbonate under various conditions. Upon being fully characterized by TPR, TPD, BET, SEM, XRD, and XPS methodologies, it is found that the bimetallic composite is effectively alloyed and well immobilized inside or outside the pore of diatomite. Under the optimal conditions of 1.2 MPa and 120∘C, the prepared catalyst with loading of 15% exhibited the highest methanol conversion of 6.50% with DMC selectivity of 91.2% as well as more than 10-hour lifetime. The possible reaction mechanism was proposed and discussed in detail. To our knowledge, this is the first report to use diatomite as a catalyst support for direct DMC synthesis from methanol and CO2.

  20. Highly efficient removal of chromium(VI) by Fe/Ni bimetallic nanoparticles in an ultrasound-assisted system.

    Science.gov (United States)

    Zhou, Xiaobin; Jing, Guohua; Lv, Bihong; Zhou, Zuoming; Zhu, Runliang

    2016-10-01

    Highly active Fe/Ni bimetallic nanocomposites were prepared by using the liquid-phase reduction method, and they were proven to be effective for Cr(VI) removal coupled with US irradiation. The US-assisted Fe/Ni bimetallic system could maintain a good performance for Cr(VI) removal at a wide pH range of 3-9. Based on the characterization of the Fe/Ni nanoparticles before and after reaction, the high efficiency of the mixed system could attribute to the synergistic effects of the catalysis of Ni(0) and US cavitation. Ni(0) could facilitate the Cr(VI) reduction through electron transfer and catalytic hydrogenation. Meanwhile, US could fluidize the Fe/Ni nanoparticles to increase the actual reactive surface area and clean off the co-precipitated Fe(III)-Cr(III) hydroxides to maintain the active sites on the surface of the Fe/Ni nanoparticles. Thus, compared with shaking, the US-assisted Fe/Ni system was more efficient on Cr(VI) removal, which achieved 94.7% removal efficiency of Cr(VI) within 10 min. The pseudo-first-order rate constant (kobs) in US-assisted Fe/Ni system (0.5075 min(-1)) was over 5 times higher than that under shaking (0.0972 min(-1)). Moreover, the Fe/Ni nanoparticles still have a good performance under US irradiation after 26 days aging as well as regeneration. Copyright © 2016 Elsevier Ltd. All rights reserved.

  1. Synergistic effect in the oxidation of benzyl alcohol using citrate-stabilized gold bimetallic nanoparticles supported on alumina

    Science.gov (United States)

    Gómez-Villarraga, Fernando; Radnik, Jörg; Martin, Andreas; Köckritz, Angela

    2016-06-01

    Bimetallic nanoparticles (NPs) containing gold and various second metals ( M = Pd, Pt, Cu, and Ag) supported on alumina (AuM/Alumina) were prepared using sodium citrate as stabilizer. In addition, supported monometallic Au/Alumina and Pd/Alumina were synthesized and tested to reveal synergistic effects in the catalytic evaluation of the bimetallic catalysts. The monometallic and bimetallic NPs revealed average sizes below 10 nm. The oxidation of benzyl alcohol with molecular oxygen as oxidant at mild conditions in liquid phase in the absence and presence (toluene or NaOH aqueous solution, 0.2 M) of a solvent was selected as test reaction to evaluate the catalytic properties of the above-mentioned solids. AuPd/Alumina exhibited the best catalytic activity among all bimetallic catalysts using toluene as solvent and under solvent-free conditions, respectively. In comparison to the monometallic catalysts, a synergistic effect with AuPd/Alumina was only evident in the solvent-free reaction. The AuPd/Alumina catalyst was able to oxidize benzyl alcohol selectively depending on the reaction medium into benzaldehyde (toluene or solvent-free) or benzoic acid (NaOH aqueous solution, 0.2 M). However, the catalyst deactivated due to particle growth of the bimetallic AuPd NPs by Ostwald ripening and leaching was not observed in the oxidation using toluene as solvent. The size of the catalytically active NPs, the metal composition of the particles, and the reaction conditions greatly influenced the catalytic oxidation results.

  2. Effect of mono- and bimetallic nanoparticles Fe, Ni, & Fe/Ni based on carbon nanocomposites on electrocatalytic properties of anodes

    Science.gov (United States)

    Ranabhat, K.; Pylinina, A. I.; Skripkin, K. S.; Sofronova, E. A.; Revina, A. A.; Kasatkin, V. E.; Patrikeev, L. N.; Lapshinsky, V. A.

    2016-10-01

    The optical properties of metallic Fe nanoparticles (NPs), Ni NPs and bimetallic Fe/Ni NPs produced under radiolysis in anaerobic condition based on a chemical reduction in the presence of oxygen and quercetin in reversed micellar solutions, and electrokinetic properties of nanoparticles carbon-based nanocomposites were studied. The possibility of the preparation of coating using different nanocomposites with anomalous electrocatalytic is addressed.

  3. Highly selective bimetallic Pt-Cu/Mg(Al)O catalysts for the aqueous-phase reforming of glycerol

    NARCIS (Netherlands)

    Boga, D.A.; Oord, R.; Beale, A.M.; Chung, Y.M.; Bruijnincx, P.C.A.; Weckhuysen, B.M.

    2013-01-01

    Monometallic Pt and bimetallic Pt-Cu catalysts supported on Mg(Al)O mixed oxides, obtained by calcination of the corresponding layered double hydroxides (LDHs), were prepared and tested in the aqueous-phase reforming (APR) of glycerol. The effect of the Mg/Al ratio and calcination temperature of the

  4. Kinetic limitations in surface alloy formation: PtCu/Ru(0001)

    Science.gov (United States)

    Engstfeld, A. K.; Jung, C. K.; Behm, R. J.

    2016-01-01

    We have systematically investigated the structure and structure formation of two-dimensional PtCu monolayer surface alloys on Ru(0001) as model systems for bimetallic PtCu catalysts and surfaces by scanning tunneling microscopy (STM). The surface alloys were prepared by deposition of Pt and Cu on Ru(0001) and thermal intermixing; different procedures were developed and tested to produce bimetallic surfaces with homogeneous structure, including also a homogeneous distribution of the different surface species, while at the same time intermixing with the Ru(0001) substrate should be inhibited. STM imaging revealed that for Pt concentrations below 65% surface alloys with homogeneous distribution could be formed, while at higher concentrations in the mixed phase, up to 82%, pure Pt or Pt-rich surface areas were formed as well. At Pt contents of 0.20 0.65 line structures were observed, but of different nature. The distribution of surface atoms in the mixed phase was evaluated from STM images with chemical contrast, the related short-range order parameters were determined. The resulting structures and their energetics, the influence of different deposition and annealing procedures and the suitability of these surfaces as model systems for studies of the surface chemistry of bimetallic PtCu surfaces are discussed.

  5. Synthesis of Ag-Au bimetallic film at liquid-liquid interface and its application in vapor sensing

    Energy Technology Data Exchange (ETDEWEB)

    Pasricha, Renu, E-mail: pasrichar@mail.nplindia.ernet.i [Material Characterization Division, National Physical Laboratory, New Delhi-110012 (India); Gupta, Shweta [Material Characterization Division, National Physical Laboratory, New Delhi-110012 (India); Sastry, M. [Tata Chemical Innovation Center, Anmol Pride, Baner Road, Pune-45 (India); Singh, Nahar; Gupta, Prabhat [Material Characterization Division, National Physical Laboratory, New Delhi-110012 (India)

    2010-11-30

    We demonstrate a novel process for preparing densely packed film of silver nanoparticles at the liquid-liquid interface followed by a transmetallation reaction with gold ion to yield a film of bimetallic nanoparticles. Films of assembled silver as well as Ag-Au bimetallic were characterized by UV-vis-spectroscopy, transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) analysis. I-V measurement shows linear behavior for both the films with ca. five orders of magnitude drop in resistance for the Ag-Au bimetallic film. Temperature dependent I-V measurement revealed a semiconductor to metal transition after transmetallation reaction. The films where checked for their potential application in chemical vapor sensing to ammonia vapors.

  6. A Systematic Investigation of p-Nitrophenol Reduction by Bimetallic Dendrimer Encapsulated Nanoparticles

    Science.gov (United States)

    2013-01-01

    We demonstrate that the reduction of p-nitrophenol to p-aminophenol by NaBH4 is catalyzed by both monometallic and bimetallic nanoparticles (NPs). We also demonstrate a straightforward and precise method for the synthesis of bimetallic nanoparticles using poly(amido)amine dendrimers. The resulting dendrimer encapsulated nanoparticles (DENs) are monodisperse, and the size distribution does not vary with different elemental combinations. Random alloys of Pt/Cu, Pd/Cu, Pd/Au, Pt/Au, and Au/Cu DENs were synthesized and evaluated as catalysts for p-nitrophenol reduction. These combinations are chosen in order to selectively tune the binding energy of the p-nitrophenol adsorbate to the nanoparticle surface. Following the Brønsted–Evans–Polanyi (BEP) relation, we show that the binding energy can reasonably predict the reaction rates of p-nitrophenol reduction. We demonstrate that the measured reaction rate constants of the bimetallic DENs is not always a simple average of the properties of the constituent metals. In particular, DENs containing metals with similar lattice constants produce a binding energy close to the average of the two constituents, whereas DENs containing metals with a lattice mismatch show a bimodal distribution of binding energies. Overall, in this work we present a uniform method for synthesizing pure and bimetallic DENs and demonstrate that their catalytic properties are dependent on the adsorbate’s binding energy. PMID:23616909

  7. The formation mechanism of bimetallic PtRu alloy nanoparticles in solvothermal synthesis.

    Science.gov (United States)

    Mi, Jian-Li; Nørby, Peter; Bremholm, Martin; Becker, Jacob; Iversen, Bo B

    2015-10-21

    An understanding of the nucleation and growth mechanism of bimetallic nanoparticles in solvothermal synthesis is important for further development of nanoparticles with tailored nanostructures and properties. Here the formation of PtRu alloy nanoparticles in a solvothermal synthesis using metal acetylacetonate salts as precursors and ethanol as both the solvent and reducing agent has been studied by in situ synchrotron radiation powder X-ray diffraction (SR-PXRD). Unlike the classical mechanism for the synthesis of monodisperse sols, the nucleation and growth processes of bimetallic PtRu nanoparticles occur simultaneously under solvothermal conditions. In the literature co-reduction of Pt and Ru is often assumed to be required to form PtRu bimetallic nanocrystals, but it is shown that monometallic Pt nanocrystals nucleate first and rapidly grow to an average size of 5 nm. Subsequently, the PtRu bimetallic alloy is formed in the second nucleation stage through a surface nucleation mechanism related to the reduction of Ru. The calculated average crystallite size of the resulting PtRu nanocrystals is smaller than that of the primary Pt nanocrystals due to the large disorder in the PtRu alloyed structure.

  8. Versatile Optimization of Chemical Ordering in Bimetallic Nanoparticles

    KAUST Repository

    Kovács, Gábor

    2017-01-05

    Chemical ordering in bimetallic nanocrystallites can now be efficiently determined by density-functional calculations with the help of topological energy expressions. Herein, we deal with extending the usage of that computational scheme. We show that it enables one to structurally characterize bimetallic nanoparticles of less regular shapes than previously studied magic-type particles. In fcc Pd–Au particles of different shapes (cuboctahedral Pd58Au58, C3v Pd61Au61, cubic Pd68Au67, and truncated octahedral Pd70Au70), we identify the surface segregation of gold as the driving force to the lowest-energy chemical ordering. We applied the calculated descriptor values quantifying the segregation propensity of Au and energies of Pd–Au bonds in these ∼1.5 nm large particles to optimize and analyze the chemical ordering in 3.7–6 nm large Pd–Au particles. We also discuss how to predict the chemical ordering in nanoalloys at elevated temperatures. The present study paves the way to advanced structural investigations of nanoalloys to substantially accelerate their knowledge-driven engineering and manufacturing.

  9. Bimetallic Pt-Ni catalysts supported on usy zeolite for n-hexane isomerization

    OpenAIRE

    F. V. Barsi; Cardoso,D.

    2009-01-01

    Isomerization of linear alkanes has had considerable importance for the refining industry because the isomers formed in this reaction have high octane number. Most works reported in the literature studied the use of bifunctional catalysts, i.e., ones that have acid sites and metallic sites. In this study, bifunctional monometallic (Ni or Pt) and bimetallic catalysts (Pt-Ni), using HUSY zeolite as the support, were prepared in order to verify the role of the metal content and composition on th...

  10. XPS and FTIR investigation of the surface properties of different prepared titania nano-powders

    DEFF Research Database (Denmark)

    Jensen, Henrik; Solovyev, Alexey; Lie, Zheshen

    2005-01-01

    oxygen (29%) and sol–gel prepared powder showed the greatest amount of surface oxygen (66%) in the form of surface hydroxyl groups. The remaining oxygen was identified as lattice oxygen. The powder prepared by the sol–gel method contained carbon impurities originating from residual alkoxy groups....... Supercritical sol–gel prepared powder and powder prepared by the sulphate method revealed same trends regarding oxygen composition with 44–47% being surface oxygen; neither contained carbon impurities. The results obtained from XPS were confirmed by FTIR measurements....

  11. Facile Fabrication of Composition-Tuned Ru-Ni Bimetallics in Ordered Mesoporous Carbon for Levulinic Acid Hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Ying; Gao, Guang; Zhang, Xin; Li, Fuwei [ChinaU - Petroleum; (Chinese Aca. Sci.)

    2016-02-04

    Bimetallic catalysts are of great importance due to their unique catalytic properties. However, their conventional synthesis requires tedious multistep procedures and prolonged synthetic time, and the resulting bimetallics usually disperse unevenly and show poor stability. It is challenging to develop a facile and step-economic synthetic methodology for highly efficient bimetallic catalysts. In this study, we report an elegant metal complex-involved multicomponent assembly route to highly efficient Ru–Ni bimetallics in ordered mesoporous carbons (OMC). The fabrication of composition-tuned Ru–Ni bimetallics in OMC (RuxNi1–x–OMC, x = 0.5–0.9) was facilely realized via in situ construction of CTAB-directed cubic Ia3d chitosan-ruthenium–nickel–silica mesophase before pyrolysis and silica removal. The resulting RuxNi1–x–OMC materials are in-depth characterized with X-ray diffraction, N2 adsorption–desorption, transmission electron microscopy, infrared spectrum, and X-ray absorption fine structure. This facile fabrication method renders homogeneously dispersed Ru–Ni bimetallics embedded in the mesoporous carbonaceous framework and creates a highly active and stable Ru0.9Ni0.1–OMC catalyst for the hydrogenation of levulinic acid (LA) to prepare γ-valerolactone (GVL), a biomass-derived platform molecule with wide application in the preparation of renewable chemicals and liquid transportation fuels. A high TOF (>2000 h–1) was obtained, and the Ru0.9Ni0.1–OMC catalyst could be used at least 15 times without obvious loss of its catalytic performance.

  12. Ni-Based Catalysts for Low Temperature Methane Steam Reforming: Recent Results on Ni-Au and Comparison with Other Bi-Metallic Systems

    Directory of Open Access Journals (Sweden)

    Anna M. Venezia

    2013-06-01

    Full Text Available Steam reforming of light hydrocarbons provides a promising method for hydrogen production. Ni-based catalysts are so far the best and the most commonly used catalysts for steam reforming because of their acceptably high activity and significantly lower cost in comparison with alternative precious metal-based catalysts. However, nickel catalysts are susceptible to deactivation from the deposition of carbon, even when operating at steam-to-carbon ratios predicted to be thermodynamically outside of the carbon-forming regime. Reactivity and deactivation by carbon formation can be tuned by modifying Ni surfaces with a second metal, such as Au through alloy formation. In the present review, we summarize the very recent progress in the design, synthesis, and characterization of supported bimetallic Ni-based catalysts for steam reforming. The progress in the modification of Ni with noble metals (such as Au and Ag is discussed in terms of preparation, characterization and pretreatment methods. Moreover, the comparison with the effects of other metals (such as Sn, Cu, Co, Mo, Fe, Gd and B is addressed. The differences of catalytic activity, thermal stability and carbon species between bimetallic and monometallic Ni-based catalysts are also briefly shown.

  13. Synthesis of Monometallic (Au and Pd) and Bimetallic (AuPd) Nanoparticles Using Carbon Nitride (C3N4) Quantum Dots via the Photochemical Route for Nitrophenol Reduction.

    Science.gov (United States)

    Fageria, Pragati; Uppala, Shravan; Nazir, Roshan; Gangopadhyay, Subhashis; Chang, Chien-Hsiang; Basu, Mrinmoyee; Pande, Surojit

    2016-10-04

    In this study, we report the synthesis of monometallic (Au and Pd) and bimetallic (AuPd) nanoparticles (NPs) using graphitic carbon nitride (g-C3N4) quantum dots (QDs) and photochemical routes. Eliminating the necessity of any extra stabilizer or reducing agent, the photochemical reactions have been carried out using a UV light source of 365 nm where C3N4 QD itself functions as a suitable stabilizer as well as a reducing agent. The g-C3N4 QDs are excited upon irradiation with UV light and produce photogenerated electrons, which further facilitate the reduction of metal ions. The successful formation of Au, Pd, and AuPd alloy nanoparticles is evidenced by UV-vis, powder X-ray diffraction, X-ray photon spectroscopy, and energy-dispersive spectroscopy techniques. The morphology and distribution of metal nanoparticles over the C3N4 QD surface has been systematically investigated by high-resolution transmission electron microscopy (HRTEM) and SAED analysis. To explore the catalytic activity of the as-prepared samples, the reduction reaction of 4-nitrophenol with excellent performance is also investigated. It is noteworthy that the synthesis of both monometallic and bimetallic NPs can be accomplished by using a very small amount of g-C3N4, which can be used as a promising photoreducing material as well as a stabilizer for the synthesis of various metal nanoparticles.

  14. Synthesis and Characterization of Optically Active Fractal Seed Mediated Silver Nickel Bimetallic Nanoparticles

    Directory of Open Access Journals (Sweden)

    Joseph Adeyemi Adekoya

    2014-01-01

    Full Text Available The synthesis of new seed mediated AgNi allied bimetallic nanocomposites was successfully carried out by the successive reduction of the metal ions in diethylene glycol, ethylene glycol, glycerol, and pentaerythritol solutions, with concomitant precipitation of Ag/Ni bimetal sols. The optical measurement revealed the existence of distinct band edge with surface plasmon resonance (SPR in the region of 400–425 nm and excitonic emission with maximum peak at 382 nm which were reminiscent of cluster-in-cluster surface enriched bimetallic silver-nickel sols. The morphological characterization by transmission electron microscopy, high resolution transmission electron microscopy, and X-ray diffraction analyses complimented by surface scan using X-ray photoelectron spectroscopy strongly supported the formation of intimately alloyed face-centered silver/nickel nanoclusters.

  15. Computer-assisted electrochemical fabrication of a highly selective and sensitive amperometric nitrite sensor based on surface decoration of electrochemically reduced graphene oxide nanosheets with CoNi bimetallic alloy nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Gholivand, Mohammad-Bagher, E-mail: mbgholivand2013@gmail.com [Faculty of Chemistry, Razi University, Kermanshah 671496734 (Iran, Islamic Republic of); Jalalvand, Ali R. [Faculty of Chemistry, Razi University, Kermanshah 671496734 (Iran, Islamic Republic of); Laboratorio de Desarrollo Analítico y Quimiometría (LADAQ), Cátedra de Química Analítica I, Universidad Nacional del Litoral, Ciudad Universitaria, CC 242 (S3000ZAA), Santa Fe (Argentina); Goicoechea, Hector C. [Laboratorio de Desarrollo Analítico y Quimiometría (LADAQ), Cátedra de Química Analítica I, Universidad Nacional del Litoral, Ciudad Universitaria, CC 242 (S3000ZAA), Santa Fe (Argentina)

    2014-07-01

    For the first time, a novel, robust and very attractive statistical experimental design (ED) using minimum-run equireplicated resolution IV factorial design (Min-Run Res IV FD) coupled with face centered central composite design (FCCCD) and Derringer's desirability function (DF) was developed to fabricate a highly selective and sensitive amperometric nitrite sensor based on electrodeposition of CoNi bimetallic alloy nanoparticles (NPs) on electrochemically reduced graphene oxide (ERGO) nanosheets. The modifications were characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), energy dispersive X-ray spectroscopic (EDS), scanning electron microscopy (SEM) techniques. The CoNi bimetallic alloy NPs were characterized using digital image processing (DIP) for particle counting (density estimation) and average diameter measurement. Under the identified optimal conditions, the novel sensor detects nitrite in concentration ranges of 0.1–30.0 μM and 30.0–330.0 μM with a limit of detection (LOD) of 0.05 μM. This sensor selectively detects nitrite even in the presence of high concentration of common ions and biological interferents therefore, we found that the sensor is highly selective. The sensor also demonstrated an excellent operational stability and good antifouling properties. The proposed sensor was used to the determination of nitrite in several foodstuff and water samples. - Highlights: • Eight variables were screened by Min Run Res IV FD to identify the key variables. • Mathematical models for the two studied responses were developed by FCCCD. • By using DF the responses were optimized simultaneously. • The SEM image of the modified electrode was processed by digital image processing. • The sensor was successfully applied to determination of nitrite in real samples.

  16. Preparation of Au-Pt nanostructures by combining top-down with bottom-up strategies and application in label-free electrochemical immunosensor for detection of NMP22.

    Science.gov (United States)

    Jia, Hongying; Gao, Picheng; Ma, Hongmin; Wu, Dan; Du, Bin; Wei, Qin

    2015-02-01

    A novel label-free amperometric immunosensor for sensitive detection of nuclear matrix protein 22 (NMP22) was developed based on Au-Pt bimetallic nanostructures, which were prepared by combining top-down with bottom-up strategies. Nanoporous gold (NPG) was prepared by "top-down" dealloying of commercial Au/Ag alloy film. After deposition of NPG on an electrode, Pt nanoparticles (PtNPs) were further decorated on NPG by "bottom-up" electrodeposition. The prepared bimetallic nanostructures combine the merits of both NPG and PtNPs, and show a high electrocatalytic activity towards the reduction of H2O2. The label-free immunosensor was constructed by directly immobilizing antibody of NMP22 (anti-NMP22) on the surface of bimetallic nanostructures. The immunoreaction induced amperometric response could be detected and negatively correlated to the concentration of NMP22. Bimetallic nanostructure morphologies and detection conditions were investigated to obtain the best sensing performance. Under the optimal conditions, a linear range from 0.01ng/mL to 10ng/mL and a detection limit of 3.33pg/mL were obtained. The proposed immunosensor showed high sensitivity, good selectivity, stability, reproducibility, and regeneration for the detection of NMP22, and it was evaluated in urine samples, receiving satisfactory results.

  17. Contamination and Surface Preparation Effects on Composite Bonding

    Science.gov (United States)

    Kutscha, Eileen O.; Vahey, Paul G.; Belcher, Marcus A.; VanVoast, Peter J.; Grace, William B.; Blohowiak, Kay Y.; Palmieri, Frank L.; Connell, John W.

    2017-01-01

    Results presented here demonstrate the effect of several prebond surface contaminants (hydrocarbon, machining fluid, latex, silicone, peel ply residue, release film) on bond quality, as measured by fracture toughness and failure modes of carbon fiber reinforced epoxy substrates bonded in secondary and co-bond configurations with paste and film adhesives. Additionally, the capability of various prebond surface property measurement tools to detect contaminants and potentially predict subsequent bond performance of three different adhesives is also shown. Surface measurement methods included water contact angle, Dyne solution wettability, optically stimulated electron emission spectroscopy, surface free energy, inverse gas chromatography, and Fourier transform infrared spectroscopy with chemometrics analysis. Information will also be provided on the effectiveness of mechanical and energetic surface treatments to recover a bondable surface after contamination. The benefits and drawbacks of the various surface analysis tools to detect contaminants and evaluate prebond surfaces after surface treatment were assessed as well as their ability to correlate to bond performance. Surface analysis tools were also evaluated for their potential use as in-line quality control of adhesive bonding parameters in the manufacturing environment.

  18. The Role of Surface Preparation Parameters on Cold Roll Bonding of Aluminum Strips

    Science.gov (United States)

    Jamaati, Roohollah; Toroghinejad, Mohammad Reza

    2011-03-01

    It is the objective of this article to investigate the influence of surface preparation on the cold roll bonding (CRB) process. In this context, the effects of surface preparation parameters consisting of surface preparation method, surface roughness, scratch-brushing parameters, and the delay time between surface preparation and rolling are investigated on the bond strength of aluminum strips. The bond strength of two adjacent aluminum strips produced by the CRB process is evaluated by the peeling test. Furthermore, the interface region is investigated by metallographic observations. Our findings indicate that higher surface roughness values and shorter delay times improve the bond strength. It is also found that degreasing followed by scratch-brushing yield the best bonding properties.

  19. Enhanced dechlorination of trichloroethylene using electrospun polymer nanofibrous mats immobilized with iron/palladium bimetallic nanoparticles.

    Science.gov (United States)

    Ma, Hui; Huang, Yunpeng; Shen, Mingwu; Guo, Rui; Cao, Xueyan; Shi, Xiangyang

    2012-04-15

    Fe/Pd bimetallic nanoparticles (NPs) have held great promise for treating trichloroethylene (TCE)-contaminated groundwater, without the accumulation of chlorinated intermediates. However, the conventionally used colloidal Fe/Pd NPs usually aggregate rapidly, resulting in a reduced reactivity. To reduce the particle aggregation, we employed electrospun polyacrylic acid (PAA)/polyvinyl alcohol (PVA) polymer nanofibers as a nanoreactor to immobilize Fe/Pd bimetallic NPs. In the study, the water-stable PAA/PVA nanofibrous mats were complexed with Fe (III) ions via the binding with the free carboxyl groups of PAA for subsequent formation and immobilization of zero-valent iron (ZVI) NPs. Fe/Pd bimetallic NPs were then formed by the partial reduction of Pd(II) ions with ZVI NPs. The formed electrospun nanofibrous mats containing Fe/Pd bimetallic NPs with a diameter of 2.8 nm were characterized by scanning electron microscopy, energy-dispersive spectroscopy, transmission electron microscopy, thermogravimetric analysis, and inductively coupled plasma-atomic emission spectroscopy. The Fe/Pd NP-containing electrospun PAA/PVA nanofibrous mats exhibited higher reactivity than that of the ZVI NP-containing mats or colloidal Fe/Pd NPs in the dechlorination of trichloroethylene (TCE), which was used as a model contaminant. With the high surface area to volume ratio, high porosity, and great reusability of the fibrous mats immobilized with the bimetallic NPs, the composite nanofibrous mats should be amenable for applications in remediation of various environmental contaminants. Copyright © 2011 Elsevier B.V. All rights reserved.

  20. Preparation Of Control Space For Remeshing Of Polygonal Surfaces

    OpenAIRE

    Tomasz Jurczyk; Barbara Glut

    2013-01-01

    The subject of the article concerns the issues of remeshing, transforming a polygonal mesh into a triangular mesh adapted to surface. From the initial polygonal mesh the curvature of surface and boundary is retrieved and used to calculate a metric tensor varying in three-dimensional space. In the proposed approach the curvature is computed using local approximation of surfaces and curves on the basis of vertices of the polygonal mesh. An essential part of the presented remeshing procedure is...

  1. A facile strategy to synthesize bimetallic Au/Ag nanocomposite film by layer-by-layer assembly technique

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Li, E-mail: zhlisuzh@163.com [Anhui Key Laboratory of Spin Electron and Nanomaterials (Cultivating Base), Suzhou University, Suzhou 234000 (China); Wang Cong; Zhang Yi [Anhui Key Laboratory of Spin Electron and Nanomaterials (Cultivating Base), Suzhou University, Suzhou 234000 (China)

    2012-05-01

    A facile strategy has been developed for the preparation of bimetallic gold-silver (Au-Ag) nanocomposite films by alternating absorption of poly-(ethyleneimine)-silver ions and Au onto substrates and subsequent reduction of the silver ions. The composition, micro-structure and properties of the {l_brace}PEI-Ag/Au{r_brace}{sub n} nanocomposite films were characterized by ultraviolet visible spectroscopy (UV-vis), transmisson electron microscopy (TEM), field emission scanning electron microscopy (FESEM), X-ray photoelectron spectroscopy (XPS), surface enhanced Raman scattering (SERS) and cyclic voltammetry (CV). The UV-vis characteristic absorbances of {l_brace}PEI-Ag/Au{r_brace}{sub n} nanocomposite thin film increase almost linear with the number of bilayers, which indicates a process of uniform assembling. Appearance of a double plasmon bands in the visible region and the lack of apparent core-shell structures in the TEM images confirm the formation of bimetallic Au-Ag nanoparticles. The result of XPS also demonstrates the existence of Ag and Au nanoparticles in the nanocomposite films. TEM and FESEM images show that these Ag and Au nanoparticles in the films possess sphere structure with the size of 20-25 nm. The resulting {l_brace}PEI-Ag/Au{r_brace}{sub n} films inherit the properties from both the metal Ag and Au, which exhibits a unique performance in SERS and electrocatalytic activities to the oxidation of dopamine. As a result, the {l_brace}PEI-Ag/Au{r_brace}{sub n} films are more attractive compared to {l_brace}PEI-Ag/PSS{r_brace}{sub n} and {l_brace}PEI/Au{r_brace}{sub n} films.

  2. PREPARATION AND CHARACTERIZATION OF SUPERHYDROPHOBIC FEP-TEFLON SURFACES

    NARCIS (Netherlands)

    BUSSCHER, HJ; STOKROOS, [No Value; VANDERMEI, HC; ROUXHET, PG; SCHAKENRAAD, JM

    1992-01-01

    Superhydrophobic FEP-Teflon was prepared by argon ion etching followed by oxygen glow discharge treatment of commercially available FEP-Teflon sheet material. This combined treatment yielded an increase in water contact angle from 109-degrees to > 140-degrees. Ion etching alone caused a small increa

  3. PREPARATION AND CHARACTERIZATION OF SUPERHYDROPHOBIC FEP-TEFLON SURFACES

    NARCIS (Netherlands)

    BUSSCHER, HJ; STOKROOS, [No Value; VANDERMEI, HC; ROUXHET, PG; SCHAKENRAAD, JM

    1992-01-01

    Superhydrophobic FEP-Teflon was prepared by argon ion etching followed by oxygen glow discharge treatment of commercially available FEP-Teflon sheet material. This combined treatment yielded an increase in water contact angle from 109-degrees to > 140-degrees. Ion etching alone caused a small increa

  4. Preparing bioactive surface of polystyrene with hydrophobin for trypsin immobilization

    Science.gov (United States)

    Niu, Baolong; Li, Bingzhang; Wang, Huifang; Guo, Ruijie; Liang, HaiXia; Qiao, Mingqiang; Li, Wenfeng

    2016-05-01

    A simple and reliable enzyme immobilization technique which can retain their catalytic activity for a long time is interest in many technologies. Here, the trypsin was immobilized by physisorption on polystyrene (PS) surface coated with a class I hydrophobin recombinant HGFI (rHGFI). X-ray photoelectron spectroscopy and water-contact-angle measurements demonstrated that the hydrophobicity of the PS could be well improved by rHGFI modification, and the self-assembled rHGFI showed an admirable stability on the hydrophobic PS surface against hot SDS rinsing. The enzyme activity assay illustrated that the capacity of rHGFI could enable it to well intermediate trypsin on PS surface and allow its immobilization lasting in an active form. The results obtained in this work show a way that surface modification with rHGFI should be an easy and feasible strategy for applications of enzyme-based catalytic surfaces in biosensing.

  5. In Situ Synthesis of Bimetallic Hybrid Nanocatalysts on a Paper-Structured Matrix for Catalytic Applications

    Directory of Open Access Journals (Sweden)

    Hirotaka Koga

    2011-11-01

    Full Text Available Bimetallic nanoparticles have attracted significant attention as their electrochemical and catalytic properties being superior to those of the individual component nanoparticles. In this study, gold-silver hybrid nanoparticles (AuAgNPs with an Aucore-Agshell nanostructure were successfully synthesized on zinc oxide (ZnO whiskers. The as-prepared nanocatalyst, denoted AuAgNPs@ZnO whisker, exhibits an excellent catalytic efficiency in the aqueous reduction of 4-nitrophenol to 4-aminophenol; the turnover frequency was up to 40 times higher than that of each component nanoparticle. Their unique features were attributed to the electronic ligand effect at the bimetallic interface. In addition, the AuAgNPs were synthesized on a ZnO whisker-containing paper with a fiber-network microstructure, which was prepared via a papermaking technique. The paper-structured AuAgNPs composite possessed both a paper-like practical utility and a good catalytic performance. Furthermore, the on-paper synthesis process for these bimetallic nanocatalysts is facile. These easy-to-handle nanocatalyst hybrid composites are expected to find a wide range of applications in various chemical and catalytic processes.

  6. Template-Directed Approach Towards the Realization of Ordered Heterogeneity in Bimetallic Metal-Organic Frameworks.

    Science.gov (United States)

    Kim, Daeok; Coskun, Ali

    2017-04-24

    Controlling the arrangement of different metal ions to achieve ordered heterogeneity in metal-organic frameworks (MOFs) has been a great challenge. Herein, we introduce a template-directed approach, in which a 1D metal-organic polymer incorporating well-defined binding pockets for the secondary metal ions used as a structural template and starting material for the preparation of well-ordered bimetallic MOF-74s under heterogeneous-phase hydrothermal reaction conditions in the presence of secondary metal ions such as Ni(2+) and Mg(2+) in 3 h. The resulting bimetallic MOF-74s were found to possess a nearly 1:1 metal ratio regardless of their initial stoichiometry in the reaction mixture, thus demonstrating the possibility of controlling the arrangement of metal ions within the secondary building blocks in MOFs to tune their intrinsic properties such as gas affinity. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  7. Kinetic Study on the Formation of Bimetallic Core-Shell Nanoparticles via Microemulsions

    Directory of Open Access Journals (Sweden)

    Concha Tojo

    2014-11-01

    Full Text Available Computer calculations were carried out to determine the reaction rates and the mean structure of bimetallic nanoparticles prepared via a microemulsion route. The rates of reaction of each metal were calculated for a particular microemulsion composition (fixed intermicellar exchange rate and varying reduction rate ratios between both metal and metal salt concentration inside the micelles. Model predictions show that, even in the case of a very small difference in reduction potential of both metals, the formation of an external shell in a bimetallic nanoparticle is possible if a large reactant concentration is used. The modification of metal arrangement with concentration was analyzed from a mechanistic point of view, and proved to be due to the different impact of confinement on each metal: the reaction rate of the faster metal is only controlled by the intermicellar exchange rate but the slower metal is also affected by a cage-like effect.

  8. Kinetic Study on the Formation of Bimetallic Core-Shell Nanoparticles via Microemulsions

    Science.gov (United States)

    Tojo, Concha; Vila-Romeu, Nuria

    2014-01-01

    Computer calculations were carried out to determine the reaction rates and the mean structure of bimetallic nanoparticles prepared via a microemulsion route. The rates of reaction of each metal were calculated for a particular microemulsion composition (fixed intermicellar exchange rate) and varying reduction rate ratios between both metal and metal salt concentration inside the micelles. Model predictions show that, even in the case of a very small difference in reduction potential of both metals, the formation of an external shell in a bimetallic nanoparticle is possible if a large reactant concentration is used. The modification of metal arrangement with concentration was analyzed from a mechanistic point of view, and proved to be due to the different impact of confinement on each metal: the reaction rate of the faster metal is only controlled by the intermicellar exchange rate but the slower metal is also affected by a cage-like effect. PMID:28788260

  9. What do we need for a superhydrophobic surface? A review on the recent progress in the preparation of superhydrophobic surfaces

    NARCIS (Netherlands)

    Li, X.; Reinhoudt, David; Crego Calama, Mercedes

    2007-01-01

    Superhydrophobic surfaces have drawn a lot of interest both in academia and in industry because of the self-cleaning properties. This critical review focuses on the recent progress (within the last three years) in the preparation, theoretical modeling, and applications of superhydrophobic surfaces.

  10. Effect of Surface Preparation on CLAM/CLAM Hot Isostatic Pressing diffusion bonding joints

    Science.gov (United States)

    Li, C.; Huang, Q.; Zhang, P.

    2009-04-01

    Surface preparation is essential for the Hot Isostatic Pressing (HIP) diffusion bonding of RAFM steels. Hot Isostatic Pressing (HIP) diffusion bonding experiments on China Low Activation Martensitic (CLAM) steel was performed to study the effect of surface preparation. A few approaches such as hand lapping, dry-milling and grinding etc., were used to prepare the faying surfaces of the HIP joints. Different sealing techniques were used as well. The HIP parameters were 150 MPa/3 h/1150 °C. After post HIP heat treatment (PHHT), the tensile and Charpy impact tests were carried out. The results showed that hand lapping was not suitable to prepare the faying surfaces of HIP diffusion bonding specimens although the surface roughness by hand lapping was very low.

  11. Green synthesis and characterization of Au@Pt core-shell bimetallic nanoparticles using gallic acid

    Science.gov (United States)

    Zhang, Guojun; Zheng, Hongmei; Shen, Ming; Wang, Lei; Wang, Xiaosan

    2015-06-01

    In this study, we developed a facile and benign green synthesis approach for the successful fabrication of well-dispersed urchin-like Au@Pt core-shell nanoparticles (NPs) using gallic acid (GA) as both a reducing and protecting agent. The proposed one-step synthesis exploits the differences in the reduction potentials of AuCl4- and PtCl62-, where the AuCl4- ions are preferentially reduced to Au cores and the PtCl62- ions are then deposited continuously onto the Au core surface as a Pt shell. The as-prepared Au@Pt NPs were characterized by transmission electron microscope (TEM); high-resolution transmission electron microscope (HR-TEM); scanning electron microscope (SEM); UV-vis absorption spectra (UV-vis); X-ray diffraction (XRD); Fourier transmission infrared spectra (FT-IR). We systematically investigated the effects of some experimental parameters on the formation of the Au@Pt NPs, i.e., the reaction temperature, the molar ratios of HAuCl4/H2PtCl6, and the amount of GA. When polyvinylpyrrolidone K-30 (PVP) was used as a protecting agent, the Au@Pt core-shell NPs obtained using this green synthesis method were better dispersed and smaller in size. The as-prepared Au@Pt NPs exhibited better catalytic activity in the reaction where NaBH4 reduced p-nitrophenol to p-aminophenol. However, the results showed that the Au@Pt bimetallic NPs had a lower catalytic activity than the pure Au NPs obtained by the same method, which confirmed the formation of Au@Pt core-shell nanostructures because the active sites on the surfaces of the Au NPs were covered with a Pt shell.

  12. Preparation and biocompatibility of BSA monolayer on silicon surface.

    Science.gov (United States)

    Tao, Caihong; Zhang, Junyan; Yang, Shengrong

    2011-06-01

    This paper describes a general strategy for grafting protein molecules on silicon surface by using dopamine as adhesive layer. With this method, silicon surface had been successfully modified by BSA monolayer. Fourier transform infrared spectra, X-ray photoelectron spectroscopy, contact angle analysis and atomic force microscopy confirmed the sequential grafting of initiator and protein molecules. Cell adhesion experiments with PC-12 cells showed that the obtained monolayer exhibits good biocompatibility. The corrosion resistance behavior of the polydopamine and BSA modified silicon wafers was investigated by potentiodynamic test, which indicated that the modified surfaces exhibited a better anti-corrosion capability than silicon surface. All these results must be valuable for the application of protein monolayer in biological and biomedical technology.

  13. Stainless Steel to Titanium Bimetallic Transitions

    Energy Technology Data Exchange (ETDEWEB)

    Kaluzny, J. A. [Fermilab; Grimm, C. [Fermilab; Passarelli, D. [Fermilab

    2015-01-01

    In order to use stainless steel piping in an LCLS-II (Linac Coherent Light Source Upgrade) cryomodule, stainless steel to titanium bimetallic transitions are needed to connect the stainless steel piping to the titanium cavity helium vessel. Explosion bonded stainless steel to titanium transition pieces and bimetallic transition material samples have been tested. A sample transition tube was subjected to tests and x-ray examinations between tests. Samples of the bonded joint material were impact and tensile tested at room temperature as well as liquid helium temperature. The joint has been used successfully in horizontal tests of LCLS-II cavity helium vessels and is planned to be used in LCLS-II cryomodules. Results of material sample and transition tube tests will be presented.

  14. BIMETALLIC CONDUCTOR’S SPECIFIC RESISTANCE

    Directory of Open Access Journals (Sweden)

    Markitantova Natal'ya Konstantinovna

    2013-04-01

    Full Text Available Improvement of conductors of electric energy and signals is considered by the authors. The subject of the research consists in cable conductors, and their improvement is analyzed on the macro-level. The authors have derived the final formula designated for the calculation of the value of the specific electric resistance of bimetallic conductors. MathCAD-14 software was employed to perform the calculations. The analysis of dependencies derived by the authors allowed the authors to make the conclusion that the thinner the copper layer, the higher the specific electric resistance of the bimetallic conductor. Moreover, the authors succeeded in making a quantitative presentation of the aforementioned characteristic, which is a relevant contribution into its further systemic analysis.

  15. Influence of the Au/Ag ratio on the catalytic activity of dendrimer-encapsulated bimetallic nanoparticles in microreactors

    NARCIS (Netherlands)

    Ricciardi, R.; Huskens, J.; Verboom, W.

    2015-01-01

    Dendrimer-encapsulated Au/Ag alloy nanoparticles (Au/Ag DENs) were covalently attached to a monolayer-functionalized inner surface of glass microreactors. The influence of the bimetallic alloy structure and of the different metal ratios was investigated for the reduction of 4-nitrophenol using NaBH4

  16. Influence of the Au/Ag ratio on the catalytic activity of dendrimer-encapsulated bimetallic nanoparticles in microreactors

    NARCIS (Netherlands)

    Ricciardi, R.; Huskens, Jurriaan; Verboom, Willem

    2015-01-01

    Dendrimer-encapsulated Au/Ag alloy nanoparticles (Au/Ag DENs) were covalently attached to a monolayer-functionalized inner surface of glass microreactors. The influence of the bimetallic alloy structure and of the different metal ratios was investigated for the reduction of 4-nitrophenol using

  17. Core-shell Rh-Pt nanocubes: A model for studying compressive strain effects in bimetallic nanocatalysts

    Science.gov (United States)

    Harak, Ethan William

    Shape-controlled bimetallic nanocatalysts often have increased activities and stabilities over their monometallic counterparts due to surface strain effects and electron transfer between the two metals. Here, we demonstrate that the degree of surface strain can be manipulated in shape-controlled nanocrystals through a bimetallic core shell architecture. This ability is achieved in a model core shell Rh Pt nanocube system through control of shell thickness. An increase in the Pt shell thickness leads to more compressive strain, which can increase the Pt 4f7/2 binding energy by as much as 0.13 eV. This change in electronic structure is correlated with a weakening of surface-adsorbate interactions, which we exploit to reduce catalyst poisoning by CO during formic acid electrooxidation. In fact, by precisely controlling the Pt shell thickness, the maximum current density achieved with Rh Pt nanocubes was 3.5 times greater than that achieved with similarly sized Pt nanocubes, with decreased CO generation as well. This system serves as a model for how bimetallic architectures can be used to manipulate the electronic structure of nanoparticle surfaces for efficient catalysis. The strategy employed here should enable the performance of bimetallic nanomaterials comprised of more cost-effective metals to be enhanced as well.

  18. Electrocatalysts Prepared by Galvanic Replacement

    Directory of Open Access Journals (Sweden)

    Athanasios Papaderakis

    2017-03-01

    Full Text Available Galvanic replacement is the spontaneous replacement of surface layers of a metal, M, by a more noble metal, Mnoble, when the former is treated with a solution containing the latter in ionic form, according to the general replacement reaction: nM + mMnoblen+ → nMm+ + mMnoble. The reaction is driven by the difference in the equilibrium potential of the two metal/metal ion redox couples and, to avoid parasitic cathodic processes such as oxygen reduction and (in some cases hydrogen evolution too, both oxygen levels and the pH must be optimized. The resulting bimetallic material can in principle have a Mnoble-rich shell and M-rich core (denoted as Mnoble(M leading to a possible decrease in noble metal loading and the modification of its properties by the underlying metal M. This paper reviews a number of bimetallic or ternary electrocatalytic materials prepared by galvanic replacement for fuel cell, electrolysis and electrosynthesis reactions. These include oxygen reduction, methanol, formic acid and ethanol oxidation, hydrogen evolution and oxidation, oxygen evolution, borohydride oxidation, and halide reduction. Methods for depositing the precursor metal M on the support material (electrodeposition, electroless deposition, photodeposition as well as the various options for the support are also reviewed.

  19. Preparation Of Control Space For Remeshing Of Polygonal Surfaces

    Directory of Open Access Journals (Sweden)

    Tomasz Jurczyk

    2013-01-01

    Full Text Available The subject of the article concerns the issues of remeshing, transforming a polygonal mesh into a triangular mesh adapted to surface. From the initial polygonal mesh the curvature of surface and boundary is retrieved and used to calculate a metric tensor varying in three-dimensional space. In the proposed approach the curvature is computed using local approximation of surfaces and curves on the basis of vertices of the polygonal mesh. An essential part of the presented remeshing procedure is creation of a control space structure based on the retrieved discrete data. The subsequent process of remeshing is then supervised by the contents of this auxiliary structure. The article presents various aspects related to the procedure of initialization, creation and adjusting the control space structure.

  20. Supersonic Retropulsion Surface Preparation of Carbon Fiber Reinforced Epoxy Composites for Adhesive Bonding

    Science.gov (United States)

    Palmieri, Frank L.; Belcher, Marcus A.; Wohl, Christopher J.; Blohowiak, Kay Y.; Connell, John W.

    2013-01-01

    Surface preparation is widely recognized as a key step to producing robust and predictable bonds in a precise and reproducible manner. Standard surface preparation techniques, including grit blasting, manual abrasion, and peel ply, can lack precision and reproducibility, which can lead to variation in surface properties and subsequent bonding performance. The use of a laser to ablate composite surface resin can provide an efficient, precise, and reproducible means of preparing composite surfaces for adhesive bonding. Advantages include elimination of physical waste (i.e., grit media and sacrificial peel ply layers that ultimately require disposal), reduction in process variability due to increased precision (e.g. increased reproducibility), and automation of surface preparation, all of which improve reliability and process control. This paper describes a Nd:YAG laser surface preparation technique for composite substrates and the mechanical performance and failure modes of bonded laminates thus prepared. Additionally, bonded specimens were aged in a hot, wet environment for approximately one year and subsequently mechanically tested. The results of a one year hygrothermal aging study will be presented.

  1. Laser synthesis of ligand-free bimetallic nanoparticles for plasmonic applications.

    Science.gov (United States)

    Intartaglia, R; Das, G; Bagga, K; Gopalakrishnan, A; Genovese, A; Povia, M; Di Fabrizio, E; Cingolani, R; Diaspro, A; Brandi, F

    2013-03-07

    A picosecond laser ablation approach has been developed for the synthesis of ligand-free AuAg bimetallic NPs where the relative amount of Ag is controlled in situ through a laser shielding effect. Various measurements, such as optical spectroscopy, transmission electron microscopy combined with energy dispersive X-ray spectroscopy and inductively coupled plasma optical emission spectrometry, revealed the generation of homogenous 15 nm average size bimetallic NPs with different compositions and tunable localized surface plasmon resonance. Furthermore, ligand-free metallic nanoparticles with respect to chemically synthesized nanoparticles display outstanding properties, i.e. featureless Raman background spectrum, which is a basic requirement in many plasmonic applications such as Surface Enhanced Raman Spectroscopy. Various molecules were chemisorbed on the nanoparticle and SERS investigations were carried out, by varying the laser wavelength. The SERS enhancement factor for AuAg bimetallic NPs shows an enhancement factor of about 5.7 × 10(5) with respect to the flat AuAg surface.

  2. Synthesis and characterization of highly conductive Sn-Ag bimetallic nanoparticles for printed electronics

    Energy Technology Data Exchange (ETDEWEB)

    Jo, Yun Hwan; Jung, Inyu; Kim, Na Rae; Lee, Hyuck Mo, E-mail: hmlee@kaist.ac.kr [KAIST, Department of Materials Science and Engineering (Korea, Republic of)

    2012-03-15

    To synthesize low-cost, highly conductive metal nanoparticles for inkjet printing materials, we synthesized Sn-Ag bimetallic nanoparticles using a polyol process with poly(vinyl pyrrolidone). Because a surface oxidation layer forms on Sn nanoparticles, various compositions of Sn-xAg [x = 0, 20, 40, 60, 80, 100 (wt%)] nanoparticles were synthesized and characterized for the purpose of removing the {beta}-Sn phase. The results of XPS, TEM, and XRD analyses confirm that the formation of a bimetallic phase, such as Ag{sub 4}Sn or Ag{sub 3}Sn, hinders the {beta}-Sn phase and, consequently, leads to the removal of the surface oxidation layer. To measure the sheet resistance of various compositions of Sn-Ag nanoparticles, we made the ink that contains Sn-Ag by dispersing 10 wt% of Sn-Ag nanoparticles in methanol. The sheet resistance is decreased by the conductive Sn-Ag phases, such as the fcc, Ag{sub 4}Sn, and Ag{sub 3}Sn phases, but sharply increased by the low-conductive Sn nanoparticles and the surface oxidation layer on the Sn nanoparticles. The sheet resistance results confirm that 80Ag20Sn and 60Ag40Sn bimetallic nanoparticles are suitable candidates for inkjet printing materials.

  3. Laser Surface Preparation for Adhesive Bonding of Ti-6Al-4V

    Science.gov (United States)

    Belcher, Marcus A.; List, Martina S.; Wohl, Christopher J.; Ghose, Sayata; Watson, Kent A.; Hopkins, John W.; Connell, John W.

    2010-01-01

    Adhesively bonded structures are potentially lighter in weight than mechanically fastened ones, but existing surface treatments are often considered unreliable. Two main problems in achieving reproducible and durable adhesive bonds are surface contamination and variability in standard surface preparation techniques. In this work three surface pretreatments were compared: laser etching with and without grit blasting and conventional Pasa-Jell treatment. Ti-6Al-4V surfaces were characterized by contact angle goniometry, optical microscopy, and X-ray photoelectron spectroscopy (XPS). Laser -etching was found to produce clean surfaces with precisely controlled surface topographies and PETI-5 lap shear strengths and durabilities were equivalent to those produced with Pasa-Jell.

  4. Influence of surface preparation on fusion bonding of thermoplastic composites

    NARCIS (Netherlands)

    Sacchetti, F.; Grouve, W.J.B.; Warnet, L.L.; Fernandez Villegas, I.

    2015-01-01

    Carbon fibre-reinforced thermoplastic composites laminates (CFRP) meant for fusion bonding have been moulded using different release media. The potential contamination of the laminate surface by the release media and its effect on the mechanical performance of fusion bonded joints was studied. The p

  5. Simple method for preparation of nanostructure on microchannel surface and its usage for enzyme-immobilization.

    Science.gov (United States)

    Miyazaki, Masaya; Kaneno, Jun; Uehara, Masato; Fujii, Masayuki; Shimizu, Hazime; Maeda, Hideaki

    2003-03-07

    We developed a novel preparation method of nanostructure on the microchannel surface formed by sol-gel like simple treatment with 3-aminopropyltriethoxysilane, which is suitable for a highly efficient enzyme-immobilized microchannel reactor.

  6. Bimetallic redox synergy in oxidative palladium catalysis.

    Science.gov (United States)

    Powers, David C; Ritter, Tobias

    2012-06-19

    Polynuclear transition metal complexes, which are embedded in the active sites of many metalloenzymes, are responsible for effecting a diverse array of oxidation reactions in nature. The range of chemical transformations remains unparalleled in the laboratory. With few noteworthy exceptions, chemists have primarily focused on mononuclear transition metal complexes in developing homogeneous catalysis. Our group is interested in the development of carbon-heteroatom bond-forming reactions, with a particular focus on identifying reactions that can be applied to the synthesis of complex molecules. In this context, we have hypothesized that bimetallic redox chemistry, in which two metals participate synergistically, may lower the activation barriers to redox transformations relevant to catalysis. In this Account, we discuss redox chemistry of binuclear Pd complexes and examine the role of binuclear intermediates in Pd-catalyzed oxidation reactions. Stoichiometric organometallic studies of the oxidation of binuclear Pd(II) complexes to binuclear Pd(III) complexes and subsequent C-X reductive elimination from the resulting binuclear Pd(III) complexes have confirmed the viability of C-X bond-forming reactions mediated by binuclear Pd(III) complexes. Metal-metal bond formation, which proceeds concurrently with oxidation of binuclear Pd(II) complexes, can lower the activation barrier for oxidation. We also discuss experimental and theoretical work that suggests that C-X reductive elimination is also facilitated by redox cooperation of both metals during reductive elimination. The effect of ligand modification on the structure and reactivity of binuclear Pd(III) complexes will be presented in light of the impact that ligand structure can exert on the structure and reactivity of binuclear Pd(III) complexes. Historically, oxidation reactions similar to those discussed here have been proposed to proceed via mononuclear Pd(IV) intermediates, and the hypothesis of mononuclear Pd

  7. Protein adsorption on gradient surfaces on polyethylene prepared in a shielded gas plasma

    NARCIS (Netherlands)

    Spijker, Hendrikje; Bos, Roelof; van Oeveren, Willem; de Vries, Jacob; Busscher, Hendrik

    1999-01-01

    In this study, a new and simple method is described to prepare wettability gradients on polymers by means of glow discharge in a partly shielded argon plasma. The surface characteristics of thus prepared gradients on low density polyethylene were determined by contact angle measurements and electron

  8. Micro- and nano-porous surface patterns prepared by surface-confined directional melt crystallization of solvent

    Science.gov (United States)

    Kim, Byoung Soo; Kim, Hyun Jin; An, Suyeong; Chi, Sangwon; Kim, Junseok; Lee, Jonghwi

    2017-07-01

    Recently, numerous attempts have been made to engineer micro- and nano-porous surface patterns or to develop convenient preparation methods for the practical applications of self-cleaning surfaces, water-repellent surfaces, novel textures, etc. Herein, we introduce a simple, cheap, and repeatable crystallization-based method to produce porous surface structures, on any surface of already fabricated polymeric materials. Contact of the solvent phase with cooled polymer surfaces enabled the limited dissolution of the surfaces and the subsequent extremely fast melt crystallization of the solvent. After removing the crystals, various micro- and nano-porous patterns were obtained, whose pore sizes ranged over three orders of magnitude. Pore depth was linearly dependent on the dissolution time. Crystal growth was mainly directed normal to the surfaces, but it was also controlled in-plane, resulting in cylindrical or lamellar structures. Superhydrophobic surfaces were successfully prepared on both polystyrene and polycarbonate. This process offers a novel surface engineering tool for a variety of polymer surfaces, whose topology can be conveniently controlled over a wide range by crystal engineering.

  9. Preparation and Properties of Zirconium Hydride on the Surface of MCM-41 Mesoporous Molecular Sieves

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Zirconium monohydride bonded to the framework oxygen of MCM-41 surface was prepared by the reaction of tetraneopentyl zirconium with MCM-41 surface hydroxyl groups, followed by the hydrogenolysis of the resulted product. The surface hydride was characterized by using infrared spectroscopy, solid-state NMR, elemental analysis, gas-phase chromatography and chemical probing reaction. It was shown that this surface species is stable below 150 ℃ and can catalytically crack alkanes into methane and ethane at 100 ℃.

  10. Investigation of Surface Preparations to Enhance Photon Doppler Velocimetry Measurements

    Science.gov (United States)

    2015-08-01

    Illustration depicting differences between a specular reflector (left) and a diffuse reflector (right). Solid blue arrows portray incident light rays and...explain the results obtained. When a surface is finished with a smooth, flat finish the reflection pattern tends toward that of a specular reflector...between a specular reflector (left) and a diffuse reflector (right). Solid blue arrows portray incident light rays and dashed red arrows portray

  11. Preparation of Chemical Samples On Relevant Surfaces Using Inkjet Technology

    Science.gov (United States)

    2013-04-01

    moisture is absorbed by the chemical from the air. The weight eventually stabilizes as the chemical moisture content approaches that of the air. This...when similar chemical solutions are paint -sprayed onto a hot (70 °C) substrate, the crystals are smaller, more numerous, and more closely spaced. To...gravity, surface tension, particle size, and chemical composition. Substrate material may be wood, metal, glass, plastic, concrete, road blacktop, dirt

  12. One step electrochemical synthesis of bimetallic PdAu supported on nafion–graphene ribbon film for ethanol electrooxidation

    Energy Technology Data Exchange (ETDEWEB)

    Shendage, Suresh S., E-mail: sureshsshendage@gmail.com; Singh, Abilash S.; Nagarkar, Jayashree M., E-mail: jm.nagarkar@ictmumbai.edu.in

    2015-10-15

    Highlights: • Electrochemical deposition of bimetallic PdAu NPs. • Highly loaded PdAu NPs are obtained. • Nafion–graphene supported PdAu NPs shows good activity for ethanol electrooxidation. - Abstract: A nafion–graphene ribbon (Nf–GR) supported bimetallic PdAu nanoparticles (PdAu/Nf–GR) catalyst was prepared by electrochemical codeposition of Pd and Au at constant potential. The prepared catalyst was characterized by scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDAX), transmission electron microscopy (TEM) and X-ray diffraction analysis (XRD). The average particle size of PdAu nanoparticles (NPs) determined from XRD was 3.5 nm. The electrocatalytic activity of the PdAu/Nf–GR catalyst was examined by cyclic voltametry. It was observed that the as prepared catalyst showed efficient activity and good stability for ethanol electrooxidation in alkaline medium.

  13. Structure and atomic vibrations in bimetallic Ni13 - n Al n clusters

    Science.gov (United States)

    Rusina, G. G.; Borisova, S. D.; Chulkov, E. V.

    2015-04-01

    The binding energy, equilibrium geometry, and vibration frequencies in bimetallic clusters Ni13 - n Al n ( n = 0-13) have been calculated using the embedded atom method potentials. It has been shown that the icosahedral structure is the most stable in monoatomic and bimetallic clusters. A tendency of Al atoms to segregate on the cluster surface has been revealed in agreement with the experimental data. The calculations of the atomic vibrations have shown the nonmonotonic dependence of the minimum and maximum vibration frequencies of cluster atoms on its composition and the coupling of their extreme values with the most stable atomic configuration. The increase in the number of Al atoms leads to the shift of the frequency spectrum and the substantial redistribution of the localization of vibrations on the cluster atoms.

  14. Preparation of Zirconia-Ceria Powders with High Specific Surface Area

    Institute of Scientific and Technical Information of China (English)

    Wang Enguo; Mei Fang

    2004-01-01

    Zirconia-ceria mixed oxide powders were prepared by high temperature aging method.The effects of the temperature and the time of aging, cerium content and calcination on powder performance were studied.The result shows that high temperature aging is an efficient way of preparation of ZrO2-CeO2 mixed oxide powders with high specific surface area and good thermal stability, and that addition of a small amount of cerium to hydrous zirconia can promote the preparation of high specific surface area powders.

  15. Copper-silver bimetallic system on natural clinoptilolite: thermal reduction of Cu2+ and Ag+ exchanged.

    Science.gov (United States)

    Rodríguez-Iznaga, Inocente; Petranovskii, Vitalii; Castillón-Barraza, Felipe; Concepción-Rosabal, Beatriz

    2011-06-01

    Copper-silver bimetallic system supported on natural clinoptilolite from Tasajeras deposit (Cuba) was studied. Bimetallic samples were prepared by simultaneous ion exchange, and reduced in a wide temperature range in a hydrogen flow. The main goal of the work was analysis of the mutual influence of both metals on their reduction process and the properties of the resultant particles. Analysis was done by combined use of XRD and UV-Vis spectroscopy. The reduction of Cu2+ and Ag+ cations shows existence of notable inter-influence between both cations during this process. The Cu2+ reduction is favored by the presence of Ag+, which should be related with the synergetic influence of silver cations and/or clusters formed on the first stages of reduction on Cu(2+)-framework interaction, facilitating the Cu2+ reduction even at low temperature (25 and 50 degrees C). The aggregation of the reduced highly dispersed species both for copper and silver is limited in this bimetallic system. The introduction of Ag+ as the second cation in the copper-exchanged zeolites favors the copper reduction at lower temperatures (25 and 50 degrees C), and appears to be the efficient tool for the control of the size of the resultant reduced nanoparticles (it means their dispersion).

  16. Ionic liquid assisted synthesis of Au-Pd bimetallic particles with enhanced electrocatalytic activity.

    Science.gov (United States)

    Li, Zhonghao; Li, Rui; Mu, Tiancheng; Luan, Yuxia

    2013-05-03

    Morphology- and composition-controlled synthesis of Au-Pd bimetallic particles was realized by a facile ionic liquid assisted route at room temperature. The morphologies of the synthesized particles, such as nanoflake-constructed spheres with a core-shell structure, nanoparticle-constructed spheres, and nanoparticle-constructed dendrites, could be well controlled by the present route. The ionic liquid was found to play a key role in the formation of these interesting particles. Moreover, the composition (Au:Pd) of the particles could be modulated by means of the molar ratio of the metal precursors in the feeding solutions. The Au-Pd bimetallic particles exhibit high electrocatalytic activity toward oxidation of ethanol and formic acid. Furthermore, cyclic voltammetric studies on the as-prepared Au-Pd bimetallic particles revealed good electroactivity for H2O2, which results in an effective amperometric H2O2 sensor. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. Monodispersed bimetallic PdAg nanoparticles with twinned structures: formation and enhancement for the methanol oxidation.

    Science.gov (United States)

    Yin, Zhen; Zhang, Yining; Chen, Kai; Li, Jing; Li, Wenjing; Tang, Pei; Zhao, Huabo; Zhu, Qingjun; Bao, Xinhe; Ma, Ding

    2014-03-10

    Monodispersed bimetallic PdAg nanoparticles can be fabricated through the emulsion-assisted ethylene glycol (EG) ternary system. Different compositions of bimetallic PdAg nanoparticles, Pd₈₀Ag₂₀, Pd₆₅Ag₃₅ and Pd₄₆Ag₅₄ can be obtained via adjusting the reaction parameters. For the formation process of the bimetallic PdAg nanoparticles, there have two-stage growth processes: firstly, nucleation and growth of the primary nanoclusters; secondly, formation of the secondary nanoparticles with the size-selection and relax process via the coalescence or aggregation of the primary nanoclusters. The as-prepared PdAg can be supported on the carbon black without any post-treatment, which exhibited high electro-oxidation activity towards methanol oxidation under alkaline media. More importantly, carbon-supported Pd₈₀Ag₂₀ nanoparticles reveal distinctly superior activities for the methanol oxidation, even if compared with commercial Pt/C electro-catalyst. It is concluded that the enhanced activity is dependant on the unique twinning structure with heterogeneous phase due to the dominating coalescence growth in EG ternary system.

  18. Cation exchange resin immobilized bimetallic nickel-iron nanoparticles to facilitate their application in pollutants degradation.

    Science.gov (United States)

    Ni, Shou-Qing; Yang, Ning

    2014-04-15

    Nanoscale zerovalent iron (nZVI) usually suffers from reduction of reactivity by aggregation, difficulty of assembling, environmental release and health concerns. Furthermore, data are lacking on the effect of cheap nickel on debromination of decabromodiphenyl ether (DBDE) by immobilized nZVI in aqueous system. In this study, strong acid polystyrene cation-exchange resins with particle diameter from 0.4 to 0.6 mm were utilized as matrices to immobilize bimetallic nickel-iron nanoparticles in order to minimize aggregation and environmental leakage risks of nZVI and to enhance their reactivity. Elemental distribution mapping showed that iron particles distributed uniformly on the surface of the resin and nickel particles were dispersed homogeneously into Fe phase. The reaction rate of resin-bound nZVI is about 55% higher than that of dispersed nZVI. The immobilized bimetallic nanoparticles with 9.69% Ni had the highest debromination percent (96%) and reaction rate (0.493 1/h). The existence of Ni significantly improved the debromination rate, due to the surface coverage of catalytic metal on the reductive metal and the formation of a galvanic cell. The environmental dominant congeners, such as BDE 154, 153, 100, 99 and 47, were produced during the process. Outstanding reactive performance, along with magnetic separation assured that resin-bound bimetallic nickel-iron nanoparticles are promising material that can be utilized to remediate a wide variety of pollutants contaminated sites including polybrominated diphenyl ethers. Copyright © 2014 Elsevier Inc. All rights reserved.

  19. How to Determine the Core-Shell Nature in Bimetallic Catalyst Particles?

    Directory of Open Access Journals (Sweden)

    Emma Westsson

    2014-11-01

    Full Text Available Nanometer-sized materials have significantly different chemical and physical properties compared to bulk material. However, these properties do not only depend on the elemental composition but also on the structure, shape, size and arrangement. Hence, it is not only of great importance to develop synthesis routes that enable control over the final structure but also characterization strategies that verify the exact nature of the nanoparticles obtained. Here, we consider the verification of contemporary synthesis strategies for the preparation of bimetallic core-shell particles in particular in relation to potential particle structures, such as partial absence of core, alloying and raspberry-like surface. It is discussed what properties must be investigated in order to fully confirm a covering, pin-hole free shell and which characterization techniques can provide such information. Not uncommonly, characterization strategies of core-shell particles rely heavily on visual imaging like transmission electron microscopy. The strengths and weaknesses of various techniques based on scattering, diffraction, transmission and absorption for investigating core-shell particles are discussed and, in particular, cases where structural ambiguities still remain will be highlighted. Our main conclusion is that for particles with extremely thin or mono-layered shells—i.e., structures outside the limitation of most imaging techniques—other strategies, not involving spectroscopy or imaging, are to be employed. We will provide a specific example of Fe-Pt core-shell particles prepared in bicontinuous microemulsion and point out the difficulties that arise in the characterization process of such particles.

  20. Cu-Co bi-metal catalyst prepared by perovskite CuO/LaCoO3 used for higher alcohol synthesis from syngas

    Institute of Scientific and Technical Information of China (English)

    Yuzhen Fang; Yuan Liu; Wei Deng; Junhai Liu

    2014-01-01

    Cu-Co bi-metal catalysts derived from CuO/LaCoO3 perovskite structure were prepared by one-step citrate complexing method, and the structure evolution reaction from CuO/LaCoO3 to Cu-Co2C/La2O2CO3 under H2 pretreatment was investigated by techniques of XRD, TPR and TEM. The results suggest that a much higher dispersion of copper significantly enhanced the reduction of cobalt, and a stronger interaction between copper and cobalt ions in LaCoO3 particles led to the formation of bi-metallic Cu-Co particles in the reduced catalysts and the enrichment of Co on the surface of bimetallic particles. The prepared catalysts were highly active and selective for the alcohol synthesis from syngas due to the presence of copper-modified Co2 C species.

  1. Bimetallic Pt-Ni catalysts supported on usy zeolite for n-hexane isomerization

    Directory of Open Access Journals (Sweden)

    F. V. Barsi

    2009-06-01

    Full Text Available Isomerization of linear alkanes has had considerable importance for the refining industry because the isomers formed in this reaction have high octane number. Most works reported in the literature studied the use of bifunctional catalysts, i.e., ones that have acid sites and metallic sites. In this study, bifunctional monometallic (Ni or Pt and bimetallic catalysts (Pt-Ni, using HUSY zeolite as the support, were prepared in order to verify the role of the metal content and composition on the catalytic properties for n-hexane isomerization. The method used for metal dispersion in the zeolite was competitive ion exchange using ammine complexes [Ni(NH36]Cl2 and [Pt(NH34]Cl2 as precursors. Four series of catalysts with constant atomic metal content had total metal amounts between 130 and 280 µmol M/g cat. Catalysts were characterized by temperature programmed reduction (TPR and subjected to catalytic evaluation for n-hexane isomerization at 250 ºC and 1 atm using H2/C6 = 9 molar ratio. TPR results show an easier reducibility of Ni+2 cations in the presence of Pt, which was evidenced by the displacement of the reduction peak of those cations towards lower temperatures in bimetallic catalysts. The bimetallic catalysts presented a higher activity in the isomerization of n-hexane when compared to the monometallic ones, as well better stability as the Pt content in the solid increases. The results of the activity as a function of the Pt content in the bimetallic catalysts show a maximum value around 50% of Pt. An addition of Pt above this critical value leads to a small decrease of the catalytic activity.

  2. Synthesis and characterization of bimetallic nanocatalysts and their application in selective hydrogenation of citral to unsaturated alcohols

    Indian Academy of Sciences (India)

    S A Ananthan; R Suresh; K Giribabu; V Narayanan

    2013-11-01

    TiO2-supported bimetallic nanocatalysts were prepared and reduced at two different temperatures, 375°C and 575°C for selective hydrogenation of citral to corresponding unsaturated alcohols (geraniol (GOL) and nerol (NOL)). The nanocatalysts were characterized by difference techniques of Fourier transform infrared spectroscopy (FT-IR), Brunauer, Emmett and Teller (BET) surface area measurement, scanning electron microscopy (SEM), Energy Dispersive X-ray Analysis (EDAX), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The prepared nanocatalysts are uniformly dispersed with an average particle size of 50-100 nm and zero valence metallic state. Catalysts reduced at higher temperature lead to an increase in selectivity toward unsaturated alcohols (GOL and NOL). The Pt-Ru/TiO2 shows higher activity compared to Pt-Pd/TiO2 and Pt-Au/TiO2 nanocatalysts. In addition, a second metal (Ru) also leads to an increase in GOL and NOL selectivity during citral hydrogenation. Partially generated oxidized second metal species due to the difference in electronegativity, strongly binds the C=O group and also paves the way for selective activation of C=O bond.

  3. Shear-bond-strength of orthodontic brackets to aged nano-hybrid composite-resin surfaces using different surface preparation.

    Science.gov (United States)

    Demirtas, Hatice Kubra; Akin, Mehmet; Ileri, Zehra; Basciftci, Faruk Ayhan

    2015-01-01

    The aim of this study was to evaluate the effects of different surface preparation methods on the shear bond strength (SBS) of orthodontic metal brackets to aged nano-hybrid resin composite surfaces in vitro. A total of 100 restorative composite resin discs, 6 mm in diameter and 3 mm thick, were obtained and treated with an ageing procedure. After ageing, the samples were randomly divided as follows according to surface preparation methods: (1)Control, (2)37% phosphoric acid gel, (3)Sandblasting, (4)Diamond bur, (5)Air-flow and 20 central incisor teeth were used for the control etched group. SBS test were applied on bonded metal brackets to all samples. SBS values and residual adhesives were evaluated. Analysis of variance showed a significant difference (phybrid composite resin surfaces.

  4. Structure of a passivated Ge surface prepared from aqueous solution.

    Energy Technology Data Exchange (ETDEWEB)

    Lyman, P. F.; Sakata, O.; Marasco, D, L.; Lee, T.-L.; Breneman, K. D.; Keane, D. T.; Bedzyk, M. J.; Materials Science Division; Northwestern Univ.; Univ. of Wisconsin at Milwaukee

    2000-08-10

    The structure of a passivating sulfide layer on Ge(001) was studied using X-ray standing waves and X-ray fluorescence. The sulfide layer was formed by reacting clean Ge substrates in (NH{sub 4}){sub 2}S solutions of various concentrations at 80{sup o}C. For each treatment, a sulfide layer containing approximately two to three monolayers (ML) of S was formed on the surface, and an ordered structure was found at the interface that contained approximately 0.4 ML of S. Our results suggest the rapid formation of a glassy GeS{sub x} layer containing 1.5-2.5 ML S residing atop a partially ordered interfacial layer of bridge-bonded S. The passivating reaction appears to be self-limited to 2-3 ML at this reaction temperature.

  5. Laser Surface Preparation of Epoxy Composites for Secondary Bonding: Optimization of Ablation Depth

    Science.gov (United States)

    Palmieri, Frank L.; Hopkins, John; Wohl, Christopher J.; Lin, Yi; Connell, John W.; Belcher, Marcus A.; Blohowiak, Kay Y.

    2015-01-01

    Surface preparation has been identified as one of the most critical aspects of attaining predictable and reliable adhesive bonds. Energetic processes such as laser ablation or plasma treatment are amenable to automation and are easily monitored and adjusted for controlled surface preparation. A laser ablation process was developed to accurately remove a targeted depth of resin, approximately 0.1 to 20 micrometers, from a carbon fiber reinforced epoxy composite surface while simultaneously changing surface chemistry and creating micro-roughness. This work demonstrates the application of this process to prepare composite surfaces for bonding without exposing or damaging fibers on the surface. Composite panels were prepared in an autoclave and had a resin layer approximately 10 micrometers thick above the fiber reinforcement. These composite panels were laser surface treated using several conditions, fabricated into bonded panels and hygrothermally aged. Bond performance of aged, experimental specimens was compared with grit blast surface treated specimens using a modified double cantilever beam test that enabled accelerated saturation of the specimen with water. Comparison of bonded specimens will be used to determine how ablation depth may affect average fracture energies and failure modes.

  6. Preparation of lanthanum fluoride nanolayers by depositing ionic layers on silicon surface

    Energy Technology Data Exchange (ETDEWEB)

    Zhuchkov, B.S.; Tolstoi, V.P.; Murin, I.V.; Kirillov, S.N. [St. Petersburg State Univ. (Russian Federation)

    1995-11-10

    The kinetics of growth of LaF{sub 3} nanolayers on silicon surface was studied. Influences due to preparation conditions (the concentration and the pH values of the solution, the time of surface treatment, the number of cycles of ionic layer deposition) were evaluated.

  7. Preparation, anti-biofouling and drag-reduction properties of a biomimetic shark skin surface

    Directory of Open Access Journals (Sweden)

    Xia Pu

    2016-04-01

    Full Text Available Shark skin surfaces show non-smoothness characteristics due to the presence of a riblet structure. In this study, biomimetic shark skin was prepared by using the polydimethylsiloxane (PDMS-embedded elastomeric stamping (PEES method. Scanning electron microscopy (SEM was used to examine the surface microstructure and fine structure of shark skin and biomimetic shark skin. To analyse the hydrophobic mechanism of the shark skin surface microstructure, the effect of biomimetic shark skin surface microstructure on surface wettability was evaluated by recording water contact angle. Additionally, protein adhesion experiments and anti-algae adhesion performance testing experiments were used to investigate and evaluate the anti-biofouling properties of the surface microstructure of biomimetic shark skin. The recorded values of the water contact angle of differently microstructured surfaces revealed that specific microstructures have certain effects on surface wettability. The anti-biofouling properties of the biomimetic shark skin surface with microstructures were superior to a smooth surface using the same polymers as substrates. Moreover, the air layer fixed on the surface of the biomimetic shark skin was found to play a key role in their antibiont adhesion property. An experiment into drag reduction was also conducted. Based on the experimental results, the microstructured surface of the prepared biomimetic shark skin played a significant role in reducing drag. The maximum of drag reduction rate is 12.5%, which is higher than the corresponding maximum drag reduction rate of membrane material with a smooth surface.

  8. Facile preparation of superhydrophobic surface with high adhesive forces based carbon/silica composite films

    Indian Academy of Sciences (India)

    Ruanbing Hu; Guohua Jiang; Xiaohong Wang; Xiaoguang Xi; Rijing Wang

    2013-11-01

    Glass substrates modified by carbon/silica composites are fabricated through a two-step process for the preparation of a superhydrophobic surface (water contact angle ≥ 150°). Carbon nanoparticles were first prepared through a deposition process on glass using a hydrothermal synthesis route, then the glass was modified by SiO2 using the hydrolysis reaction of tetraethylorthosilicate at room temperature. It is not only a facile method to create a superhydrophobic surface, but also helps to form a multi-functional surface with high adhesive forces.

  9. Structural Characterization of Bimetallic Nanocrystal Electrocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Cullen, David A [ORNL

    2016-01-01

    Late transition metal nanocrystals find applications in heterogeneous catalysis such as plasmon-enhanced catalysis and as electrode materials for fuel cells, a zero-emission and sustainable energy technology. Their commercial viability for automotive transportation has steadily increased in recent years, almost exclusively due to the discovery of more efficient bimetallic nanocatalysts for the oxygen reduction reaction (ORR) at the cathode. Despite improvements to catalyst design, achieving high activity while maintaining durability is essential to further enhance their performance for this and other important applications in catalysis. Electronic effects arising from the generation of metal-metal interfaces, from plasmonic metals, and from lattice distortions, can vastly improve sorption properties at catalytic surfaces, while increasing durability.[1] Multimetallic lattice-strained nanoparticles are thus an interesting opportunity for fundamental research.[2,3] A colloidal synthesis approach is demonstrated to produce AuPd alloy and Pd@Au core-shell nanoicosahedra as catalysts for electro-oxidations. The nanoparticles are characterized using aberration-corrected scanning transmission electron microscopy (ac-STEM) and large solid angle energy dispersive X-ray spectroscopy (EDS) on an FEI Talos 4-detector STEM/EDS system. Figure 1 shows bright-field (BF) and high-angle annular dark-field (HAADF) ac-STEM images of the alloy and core-shell nanoicosahedra together with EDS line-scans and elemental maps. These structures are unique in that the presence of twin boundaries, alloying, and core-shell morphology could create highly strained surfaces and interfaces. The shell thickness of the core-shell structures observed in HAADF-STEM images is tuned by adjusting the ratio between metal precursors (Figure 2a-f) to produce shells ranging from a few to several monolayers. Specific activity was measured in ethanol electro-oxidation to examine the effect of shell thickness on

  10. Metal segregation in supported bimetallic catalysts:. gamma. -Al/sub 2/O/sub 3/-supported CO hydrogenation catalysts prepared from RhOs/sub 3/, Rh/sub 4/, and FeOs/sub 3/ clusters

    Energy Technology Data Exchange (ETDEWEB)

    Budge, J.R.; Lucke, B.F.; Gates, B.C.; Toran, J.

    1985-02-01

    Al/sub 2/O/sub 3/-supported metals were prepared from (H/sub 2/RhOs/sub 3/(CO)/sub 10/(acetylacetonate)), (Rh/sub 4/(CO)/sub 12/), and (H/sub 2/FeOs/sub 3/(CO)/sub 13/). The samples were characterized by infrared spectroscopy after reaction with CO + H/sub 2/ and tested as catalysts for conversion of CO + H/sub 2/ in a flow reactor at 200 and 270/sup 0/C and 10 atm. Used catalysts were characterized by transmission electron microscopy, X-ray photoelectron spectroscopy, infrared spectroscopy, and elemental analysis. The catalyst lost Os during operation, presumably as a result of formation of volatile carbonyls. The catalytic reaction products were a nearly Schulz-Flory-Anderson distribution of hydrocarbons with small yields of dimethyl ether (formed from methanol). The performance of the catalyst prepared from the RhOs/sub 3/ clusters was closely similar to that of the catalyst prepared from the Rh/sub 4/ cluster. Characterization of the samples after treatment in CO + H/sub 2/ and after catalysis demonstrated that the RhOs/sub 3/ clusters broke apart, first giving triosmium clusters and mononuclear Rh complexes and then, at higher temperatures, giving Rh crystallites and mononuclear Os complexes. The catalytic activity for hydrocarbon synthesis is attributed to the Rh metal; the activity for methanol synthesis is tentatively associated with ionic Rh complexes. The FeOs/sub 3/ catalyst was two orders of magnitude less active than the Rh Os/sub 3/ catalyst, apparently consisting of small iron oxide particles and mononuclear Os complexes. The selectivity of this catalyst for dimethyl ether formation increased markedly with time onstream in the flow reactor; after 55 h, 36 mol% of the organic product was ether. 25 refs., 5 figs., 3 tabs.

  11. Preparation of Material Surface Structure Similar to Hydrophobic Structure of Lotus Leaf

    Institute of Scientific and Technical Information of China (English)

    CAO Feng; GUAN Zisheng; LI Dongxu

    2008-01-01

    Nano/micro replication,a technique widely applied in the microelectronics field,was introduced to prepare the hydrophobic bionics microstructure on material surface.Poly(vinyl alcohol)(PVA)and polystyrene(PS)moulds of the mastoid microstructure on lotus leaf surface were prepared respectively by the nano/micro replication technology.And poly(dimethylsiloxane)(PDMS)replicas with the mastoid-like microstructure were prepared from these two kinds of polymer moulds.Scanning electronic microscope(SEM) was employed to investigate the morphology and microstructures on moulds and replicas.Both the static and dynamic contact angles between water droplet and PDMS replicas'surface were also measured.As a result,similar microstructure Can be observed clearly on the surface of PDMS replicas and the static contact angle on PDMS replicas was enhanced dramatically by the existence of these microstructures.

  12. Mimicking natural superhydrophobic surfaces and grasping the wetting process: a review on recent progress in preparing superhydrophobic surfaces.

    Science.gov (United States)

    Yan, Y Y; Gao, N; Barthlott, W

    2011-12-12

    A typical superhydrophobic (ultrahydrophobic) surface can repel water droplets from wetting itself, and the contact angle of a water droplet resting on a superhydrophobic surface is greater than 150°, which means extremely low wettability is achievable on superhydrophobic surfaces. Many superhydrophobic surfaces (both manmade and natural) normally exhibit micro- or nanosized roughness as well as hierarchical structure, which somehow can influence the surface's water repellence. As the research into superhydrophobic surfaces goes deeper and wider, it is becoming more important to both academic fields and industrial applications. In this work, the most recent progress in preparing manmade superhydrophobic surfaces through a variety of methodologies, particularly within the past several years, and the fundamental theories of wetting phenomena related to superhydrophobic surfaces are reviewed. We also discuss the perspective of natural superhydrophobic surfaces utilized as mimicking models. The discussion focuses on how the superhydrophobic property is promoted on solid surfaces and emphasizes the effect of surface roughness and structure in particular. This review aims to enable researchers to perceive the inner principles of wetting phenomena and employ suitable methods for creation and modification of superhydrophobic surfaces. Copyright © 2011 Elsevier B.V. All rights reserved.

  13. Evaluation of Alternative Peel Ply Surface Preparation Methods of SC-15 Epoxy / Fiberglass Composite Surfaces for Secondary Bonding

    Science.gov (United States)

    2014-01-01

    surface preparation, secondary bonding, peel ply, film adhesive, toughened epoxy, VARTM 16. SECURITY CLASSIFICATION OF: 17. LIMITATION OF...for the VARTM process. .......................6 Figure 2. Vacuum-bagged laminate during the debulk process...processing temperature. .........................3 Table 2. ARL cure schedule for VARTM processing of SC-15

  14. Preparation of Highly Hydrophobic and Oleophobic Textile Surfaces Using Microwave-Promoted Silane Coupling (Postprint)

    Science.gov (United States)

    2010-12-01

    contact angles of 10 lL water and hexadecane sessile drops were measured on the prepared surfaces using a goniometer (DSA 100, Kruss) at 20 C. The range of...surfaces could provide significant advantages over conventional systems with regard to reducing the time and energy needs associated with conventional...FS does create a hydrophobic and oleophobic surface; however, such pre- treatment provides no discernable advantage over a single base-catalyzed

  15. Preparation of electrodes on cfrp composites with low contact resistance comprising laser-based surface pre-treatment

    KAUST Repository

    Almuhammadi, Khaled Hamdan

    2016-12-29

    Various examples are provided related to the preparation of electrodes on carbon fiber reinforced polymer (CFRP) composites with low contact resistance. Laser-based surface preparation can be used for bonding to CFRP composites. In one example, a method includes preparing a pretreated target area on a CFRP composite surface using laser pulsed irradiation and bonding an electrode to exposed fibers in the pretreated target area. The surface preparation can allow the electrode to have a low contact resistance with the CFRP composite.

  16. Formation of Cu/Pd bimetallic crystals by electrochemical deposition

    Energy Technology Data Exchange (ETDEWEB)

    Alvarez, A.E. [Instituto de Ingenieria Electroquimica y Corrosion (INIEC), Departamento de Ingenieria Quimica, Universidad Nacional del Sur, Avda. Alem 1253, 8000 Bahia Blanca (Argentina); Salinas, D.R., E-mail: dsalinas@uns.edu.a [Instituto de Ingenieria Electroquimica y Corrosion (INIEC), Departamento de Ingenieria Quimica, Universidad Nacional del Sur, Avda. Alem 1253, 8000 Bahia Blanca (Argentina)

    2010-04-15

    The early stages of the palladium electrodeposition process onto a vitreous carbon (VC) substrate as well as the deposition of Cu on such Pd/VC modified surface were investigated using classical electrochemical techniques, atomic force microscopy (AFM) and scanning electron microscopy (SEM). Within the potential range considered the kinetics of the Pd electrodeposition from a PdCl{sub 2} acid solution can be described by a model involving progressive nucleation on active sites and diffusion-controlled 3D growth. The nucleation rate constant, A{sub 0}, and the number of active sites of the substrate, N{sub 0}, were determined from the analysis of potentiostatic current transients on the basis of an existing theoretical model. The AFM images corroborated the progressive nucleation mechanism showing irregular palladium crystals randomly distributed over the VC surface, with different sizes and 3D morphological characteristics. The electrodeposition of Cu was carried out onto the characterized Pd/VC modified surface from a Cu{sup 2+} containing solution using a well defined polarization routine. The SEM/EDX images confirmed the formation of Cu/Pd bimetallic crystals uniformly distributed on the VC surface and the in situ AFM images obtained during this process corroborated that Cu formed a core-shell structure with the Pd crystals. Nevertheless, the subsequent anodic stripping produced only a partial dissolution of the Cu deposits, and therefore, the formation of a Cu/Pd alloy could be inferred.

  17. Bactericidal and catalytic performance of green nanocomposite based-on chitosan/carbon black fiber supported monometallic and bimetallic nanoparticles.

    Science.gov (United States)

    Ali, Fayaz; Khan, Sher Bahadar; Kamal, Tahseen; Anwar, Yasir; Alamry, Khalid A; Asiri, Abdullah M

    2017-08-28

    Nanoparticles were synthesized on the surface of green nanocomposite based on carbon black dispersed in chitosan (CB-CS) fibres. The nanoparticles were monometallic Co, Ag and Cu and bimetallic Co + Cu and Co + Ag. The CB-CS fibres were prepared and introduced into separate metal salt solutions containing Co(2+), Ag(+) and Cu(2+) and mixed Co(2+)+Cu(2+) and Co(2+)+Ag(+) ions. The metal ions immobilized on the surface of CB-CS were reduced using sodium borohydride (NaBH4) as reducing agent to synthesize the corresponding zero-valent metal nanoparticles-loaded CB-CS fibres. All the nanoparticles-loaded CB-CS samples were characterized using field emission-scanning electron microscopy, Fourier transform infrared spectroscopy and X-ray diffraction techniques. When tested as catalysts, the nanoparticles-loaded CB-CS showed excellent catalytic ability for the reduction of toxic and environmentally unwanted pollutants of para-nitrophenol, congo red and methyl orange dyes. Afterwards, the antimicrobial activities of virgin and metal-loaded CB-CS fibres were tested and the metal-loaded CB-CS fibres were found to be effective against Escherichia coli. In addition, the catalyst can be recovered easily by simply removing the fibres from the reaction mixture and can be recycled several times while maintaining high catalytic efficiency. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. Au-Pt bimetallic nanoparticles supported on functionalized nitrogen-doped graphene for sensitive detection of nitrite.

    Science.gov (United States)

    Li, Zhuang; An, Zhenzhen; Guo, Yongyang; Zhang, Kangning; Chen, Xiaoling; Zhang, Dongxia; Xue, Zhonghua; Zhou, Xibin; Lu, Xiaoquan

    2016-12-01

    In this work, we report a novel Au-Pt bimetallic nanoparticles (Au-PtNPs) decorated on the surface of nitrogen-doped graphene (NG) functionalized with 1, 3, 6, 8-pyrene tetra sulfonic acid sodium salt (PyTS) by direct electrodeposition method. The results of scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and electrochemical impendence spectrum (EIS) reveal that the Au-PtNPs were successfully anchored on the surface of NG sheets with a diameter of 20-40nm. Further, the prepared Au-PtNPs/PyTS-NG nanocomposite exhibits superior catalytic activity for the oxidation of nitrite. Under optimal experimental conditions, an amperometric sensor with a linear range of 0.5-1621μM and a detection limit of 0.19μM (S/N=3) for the detection of nitrite was set up and applied to real samples. Copyright © 2016 Elsevier B.V. All rights reserved.

  19. Prediction of atomic structure of Pt-based bimetallic nanoalloys by using genetic algorithm

    Science.gov (United States)

    Oh, Jung Soo; Nam, Ho-Seok; Choi, Jung-Hae; Lee, Seung-Cheol

    2013-05-01

    The atom-arrangements in Pt-based bimetallic nanoalloys were predicted by the combined use of genetic algorithm (GA) and molecular dynamics (MD) simulations. The nanoparticles of these nanoalloys were assumed to be a 3.5 nm-diameter truncated octahedron with Pt and noble metals of fixed composition ratio of 1:1. For the GA, a Python code, which concurrently linked with the MD method that uses the embedded atom method inter-atomic potentials, was developed for the prediction of the atom arrangements in these bimetallic nanoalloys. Successfully, the GA calculation predicted the core-shell structures for both Pt-Ag and Pt-Au nanoalloy, but an onion-like multilayered core-shell structure for Pt-Cu nanoalloy. The structural characteristics in the bimetallic nanoalloy were mainly due to the differences in the surface energy and cohesive energy between Pt and the other alloying metal elements and their miscibility gap and so on. Briefly, the prediction performance was analyzed to show the superior searching ability of GA.

  20. Core-size-dependent catalytic properties of bimetallic Au/Ag core-shell nanoparticles.

    Science.gov (United States)

    Haldar, Krishna Kanta; Kundu, Simanta; Patra, Amitava

    2014-12-24

    Bimetallic core-shell nanoparticles have recently emerged as a new class of functional materials because of their potential applications in catalysis, surface enhanced Raman scattering (SERS) substrate and photonics etc. Here, we have synthesized Au/Ag bimetallic core-shell nanoparticles with varying the core diameter. The red-shifting of the both plasmonic peaks of Ag and Au confirms the core-shell structure of the nanoparticles. Transmission electron microscopy (TEM) analysis, line scan EDS measurement and UV-vis study confirm the formation of core-shell nanoparticles. We have examined the catalytic activity of these core-shell nanostructures in the reaction between 4-nitrophenol (4-NP) and NaBH4 to form 4-aminophenol (4-AP) and the efficiency of the catalytic reaction is found to be increased with increasing the core size of Au/Ag core-shell nanocrystals. The catalytic efficiency varies from 41.8 to 96.5% with varying core size from 10 to 100 nm of Au/Ag core-shell nanoparticles, and the Au100/Ag bimetallic core-shell nanoparticle is found to be 12-fold more active than that of the pure Au nanoparticles with 100 nm diameter. Thus, the catalytic properties of the metal nanoparticles are significantly enhanced because of the Au/Ag core-shell structure, and the rate is dependent on the size of the core of the nanoparticles.

  1. DNA-Mediated Morphological Control of Pd-Au Bimetallic Nanoparticles.

    Science.gov (United States)

    Satyavolu, Nitya Sai Reddy; Tan, Li Huey; Lu, Yi

    2016-12-21

    Recent reports have shown that different DNA sequences can mediate the control of shapes and surface properties of nanoparticles. However, all previous studies have involved only monometallic particles, most of which were gold nanoparticles. Controlling the shape of bimetallic nanoparticles is more challenging, and there is little research into the use of DNA-based ligands for their morphological control. We report the DNA-templated synthesis of Pd-Au bimetallic nanoparticles starting from palladium nanocube seeds. The presence of different homo-oligomer DNA sequences containing 10 deoxy-ribonucleotides of thymine, adenine, cytosine, or guanine results in the growth of four distinct morphologies. Through detailed kinetic studies by absorption spectroscopy, scanning electron microscopy (SEM) and scanning transmission electron microscopy (STEM), we have determined the role of DNA in controlling Pd-Au nanoparticle growth morphologies. One major function of DNA is affecting various properties of the incoming metal atoms, including their diffusion and deposition on the Pd nanocube seed. Interestingly, nanoparticle growth in the presence of A10 follows an aggregative growth mechanism that is unique when compared to the other base oligomers. These findings demonstrate that DNA can allow for programmable control of bimetallic nanoparticle morphologies, resulting in more complex hybrid materials with different plasmonic properties. The capability to finely tune multimetallic nanoparticle morphology stems from the versatile structure that is unique to DNA in comparison to conventionally used capping agents in colloidal nanomaterial synthesis.

  2. Tuning the composition of AuPt bimetallic nanoparticles for antibacterial application.

    Science.gov (United States)

    Zhao, Yuyun; Ye, Chunjie; Liu, Wenwen; Chen, Rong; Jiang, Xingyu

    2014-07-28

    We show that bimetallic nanoparticles (NPs) of AuPt without any surface modification are potent antibiotic reagents, while pure Au NPs or pure Pt NPs display no antibiotic activities. The most potent antibacterial AuPt NPs happen to be the most effective catalysts for chemical transformations. The mechanism of antibiotic action includes the dissipation of membrane potential and the elevation of adenosine triphosphate (ATP) levels. These bimetallic NPs are unique in that they do not produce reactive oxygen species as most antibiotics do. Being non-toxic to human cells, these bimetallic noble NPs might open an entry to a new class of antibiotics. © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

  3. Fractal Dimension Calculation of a Manganese-Chromium Bimetallic Nanocomposite Using Image Processing

    Directory of Open Access Journals (Sweden)

    Amir Lashgari

    2015-01-01

    Full Text Available Bimetallic materials, which have the ability to convert heat change into mechanical movement, normally consist of two bonded strips of dissimilar metals that expand at different rates. We describe how we made a manganese-chromium (Mn-Cr bimetallic nanocomposite using the centrifuge method and a low-to-high approach. We conducted scanning electron microscope (SEM imaging, energy-dispersive X-ray spectroscopy (EDX analysis, and X-ray diffraction spectra of the nanocomposite to prove its identity. We examined how centrifuge speed, process time, and the use of an “intruder agent” affected the properties of the material. The fractal dimension is a significant factor that can be used to approximate the surface roughness, the texture segmentation, and an image of the studied compounds. We calculated the technique of fractal dimensions using image-processing values on a computer and histogram plot with the SEM image of the Mn-Cr bimetallic nanocomposite using MATLAB software. We applied the Statistical Package for the Social Sciences software for statistics data extracted from the SEM image of the nanocomposite and obtained the following results: mean = 1.778, median = 1.770, max = 1.98, min = 1.60, skewness = 0.177, range = 0.38, and harmonic mean = 1.771 for fractal dimension of the SEM image.

  4. The effect of metal cluster deposition route on structure and photocatalytic activity of mono- and bimetallic nanoparticles supported on TiO{sub 2} by radiolytic method

    Energy Technology Data Exchange (ETDEWEB)

    Klein, Marek [Department of Chemical Technology, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk (Poland); Institute of Fluid-Flow Machinery, Polish Academy of Sciences, 80-231 Gdansk (Poland); Nadolna, Joanna, E-mail: joanna.nadolna@ug.edu.pl [Department of Chemical Technology, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk (Poland); Department of Environmental Technology, University of Gdansk, 80-308 Gdansk (Poland); Gołąbiewska, Anna [Department of Chemical Technology, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk (Poland); Mazierski, Paweł [Department of Environmental Technology, University of Gdansk, 80-308 Gdansk (Poland); Klimczuk, Tomasz [Department of Solid State Physics, Faculty of Applied Physics and Mathematics, Gdansk University of Technology, 80-233 Gdansk (Poland); Remita, Hynd [Laboratoire de Chimie Physique, CNRS-UMR 8000, Université Paris-Sud, Université Paris-Saclay, 91405 Orsay (France); CNRS, Laboratoire de Chimie Physique, UMR 8000, 91405 Orsay (France); Zaleska-Medynska, Adriana [Department of Chemical Technology, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk (Poland); Department of Environmental Technology, University of Gdansk, 80-308 Gdansk (Poland)

    2016-08-15

    Highlights: • Pd-Pt decorated TiO{sub 2} shows the highest activity under visible light among all. • Concurrent addition of metal precursors results in rise of BNPs size and Vis-activity. • Subsequent addition of metal precursors enhances UV–vis stability of modified TiO{sub 2}. • Superoxide radicals are responsible for pollutants degradation over BNPs-TiO{sub 2}. - Abstract: TiO{sub 2} (P25) was modified with small and relatively monodisperse mono- and bimetallic clusters (Ag, Pd, Pt, Ag/Pd, Ag/Pt and Pd/Pt) induced by radiolysis to improve its photocatalytic activity. The as-prepared samples were characterized by X-ray fluorescence spectrometry (XRF), photoluminescence spectrometry (PL), diffuse reflectance spectroscopy (DRS), X-ray powder diffractometry (XRD), scanning transition electron microscopy (STEM) and BET surface area analysis. The effect of metal type (mono- and bimetallic modification) as well as deposition method (simultaneous or subsequent deposition of two metals) on the photocatalytic activity in toluene removal in gas phase under UV–vis irradiation (light-emitting diodes- LEDs) and phenol degradation in liquid phase under visible light irradiation (λ > 420 nm) were investigated. The highest photoactivity under Vis light was observed for TiO{sub 2} co-loaded with platinum (0.1%) and palladium (0.1%) clusters. Simultaneous addition of metal precursors results in formation of larger metal nanoparticles (15–30 nm) on TiO{sub 2} surface and enhances the Vis-induced activity of Ag/Pd-TiO{sub 2} up to four times, while the subsequent metal ions addition results in formation of metal particle size ranging from 4 to 20 nm. Subsequent addition of metal precursors results in formation of BNPs (bimetallic nanoparticle) composites showing higher stability in four cycles of toluene degradation under UV–vis. Obtained results indicated that direct electron transfer from the BNPs to the conduction band of the semiconductor is responsible for

  5. Processing surface sizing starch using oxidation, enzymatic hydrolysis and ultrasonic treatment methods--Preparation and application.

    Science.gov (United States)

    Brenner, Tobias; Kiessler, Birgit; Radosta, Sylvia; Arndt, Tiemo

    2016-03-15

    The surface application of starch is a well-established method for increasing paper strength. In surface sizing, a solution of degraded starch is applied to the paper. Two procedures have proved valuable for starch degradation in the paper mill: enzymatic and thermo-oxidative degradation. The objective of this study was to determine achievable efficiencies of cavitation in preparing degraded starch for surface application on paper. It was found that ultrasonic-assisted starch degradation can provide a starch solution that is suitable for surface sizing. The molecular composition of starch solutions prepared by ultrasonic treatment differed from that of starch solutions degraded by enzymes or by thermo-oxidation. Compared to commercial degradation processes, this resulted in intensified film formation and in greater penetration during surface sizing and ultimately in a higher starch content of the paper. Paper sized with ultrasonically treated starch solutions show the same strength properties compared to commercially sized paper.

  6. Synthetic process for preparation of high surface area electroactive compounds for battery applications

    Energy Technology Data Exchange (ETDEWEB)

    Evenson, Carl; Mackay, Richard

    2013-07-23

    A process is disclosed for the preparation of electroactive cathode compounds useful in lithium-ion batteries, comprising exothermic mixing of low-cost precursors and calcination under appropriate conditions. The exothermic step may be a spontaneous flameless combustion reaction. The disclosed process can be used to prepare any lithium metal phosphate or lithium mixed metal phosphate as a high surface area single phase compound.

  7. Final Technical Report: First Principles Investigations for the Ensemble Effects of PdAu and PtAu Bimetallic Nanocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Ruqian Wu

    2012-05-18

    Bimetallic surfaces with tunable chemical properties have attracted broad attention in recent years due to their ample potential for heterogeneous catalysis applications. The local chemical properties of constituents are strongly altered from their parent metals by 'ligand effect', a term encompassing the influences of charge transfer, orbital rehybridization and lattice strain. In comparison to the aforementioned, the 'ensemble effect' associated with particular arrangements of the active constituents have received much less attention, despite their notable importance towards the determination of reactivity and selectivity of bimetallic catalysts. We performed theoretical studies for understanding the ensemble effects on bimetallic catalysis: (i) simulations for the formation of different ensembles on PdAu and PtAu nanoclusters; (ii) studies of the size, shape, and substrate dependence of their electronic properties; and (iii) simulations for model reactions such as CO oxidation, methanol, ethylene and water dehydrogenation on PdAu and PtAu nanoclusters. In close collaboration with leading experimental groups, our theoretical research elucidated the fundamentals of Au based bimetallic nanocatalysts.

  8. BIMETALLIC LITHIUM BOROHYDRIDES TOWARD REVERSIBLE HYDROGEN STORAGE

    Energy Technology Data Exchange (ETDEWEB)

    Au, M.

    2010-10-21

    Borohydrides such as LiBH{sub 4} have been studied as candidates for hydrogen storage because of their high hydrogen contents (18.4 wt% for LiBH{sub 4}). Limited success has been made in reducing the dehydrogenation temperature by adding reactants such as metals, metal oxides and metal halides. However, full rehydrogenation has not been realized because of multi-step decomposition processes and the stable intermediate species produced. It is suggested that adding second cation in LiBH{sub 4} may reduce the binding energy of B-H. The second cation may also provide the pathway for full rehydrogenation. In this work, several bimetallic borohydrides were synthesized using wet chemistry, high pressure reactive ball milling and sintering processes. The investigation found that the thermodynamic stability was reduced, but the full rehydrogenation is still a challenge. Although our experiments show the partial reversibility of the bimetallic borohydrides, it was not sustainable during dehydriding-rehydriding cycles because of the accumulation of hydrogen inert species.

  9. Implant surface preparation in the surgical treatment of experimental peri-implantitis with autogenous bone graft and ePTFE membrane in cynomolgus monkeys

    DEFF Research Database (Denmark)

    Schou, Søren; Holmstrup, Palle; Jørgensen, Torben

    2003-01-01

    peri-implantitis; treatment; implant surface preparation; nonhuman primates; histology; stereology......peri-implantitis; treatment; implant surface preparation; nonhuman primates; histology; stereology...

  10. Measuring skew in average surface roughness as a function of surface preparation

    Science.gov (United States)

    Stahl, Mark T.

    2015-08-01

    Characterizing surface roughness is important for predicting optical performance. Better measurement of surface roughness reduces polishing time, saves money and allows the science requirements to be better defined. This study characterized statistics of average surface roughness as a function of polishing time. Average surface roughness was measured at 81 locations using a Zygo® white light interferometer at regular intervals during the polishing process. Each data set was fit to a normal and Largest Extreme Value (LEV) distribution; then tested for goodness of fit. We show that the skew in the average data changes as a function of polishing time.

  11. The influence of the base material surface preparation on the properties of thermally sprayed coatings

    Directory of Open Access Journals (Sweden)

    V. Marušić

    2010-01-01

    Full Text Available Using specimens, a research was conducted to determine the influence of the base material surface preparation for 42CrMo4 on the final coating, prior to actual thermal spraying. During thermal spraying, an Al-Ni-alloy was used as an interlayer before the actual coating with Cr-Mo-Ni. The surface hardness and the hardness distribution across the thickness of the sprayed coating were measured and the structure of respective sprayed coatings was photographed. A comparison of experimental results enabled the identification of the particular material preparation method with an optimal ratio of the satisfactory coating thickness and its hardness.

  12. Preparation of quercetin imprinted core-shell organosilicate microspheres using surface imprinting technique

    Institute of Scientific and Technical Information of China (English)

    Peng Yang; Wen Dan Hou; Hong Deng Qiu; Xia Liu; Sheng Xiang Jiang

    2012-01-01

    In this work,the quercetin imprinted core-shell microspheres were prepared using silica surface imprinting technique.A simple sol-gel procedure was used for the synthesis of the imprinted materials with 3-aminopropyltriethoxysilane as functional monomer and tetraethyl orthosilicate as crosslinker.The SEM images indicated that the MIPs shell was successfully grafted onto the silica surface.The characteristics of the molecularly imprinted polymers such as capacity,selectivity and absorption dynamic were investigated by rebinding experiments.The results showed that the prepared MIPs had good imprinting effect and adsorption amount of quercetin.

  13. Bimetallic Nanocatalysts in Mesoporous Silica for Hydrogen Production from Coal-Derived Fuels

    Energy Technology Data Exchange (ETDEWEB)

    Kuila, Debasish [North Carolina Agricultural & Technical State Univ., Greensboro, NC (United States); Ilias, Shamsuddin [North Carolina Agricultural & Technical State Univ., Greensboro, NC (United States)

    2013-02-13

    In steam reforming reactions (SRRs) of alkanes and alcohols to produce H2, noble metals such as platinum (Pt) and palladium (Pd) are extensively used as catalyst. These metals are expensive; so, to reduce noble-metal loading, bi-metallic nanocatalysts containing non-noble metals in MCM-41 (Mobil Composition of Material No. 41, a mesoporous material) as a support material with high-surface area were synthesized using one-pot hydrothermal procedure with a surfactant such as cetyltrimethylammonium bromide (CTAB) as a template. Bi-metallic nanocatalysts of Pd-Ni and Pd-Co with varying metal loadings in MCM-41 were characterized by x-ray diffraction (XRD), N2 adsorption, and Transmission electron microscopy (TEM) techniques. The BET surface area of MCM-41 (~1000 m2/g) containing metal nanoparticles decreases with the increase in metal loading. The FTIR studies confirm strong interaction between Si-O-M (M = Pd, Ni, Co) units and successful inclusion of metal into the mesoporous silica matrix. The catalyst activities were examined in steam reforming of methanol (SRM) reactions to produce hydrogen. Reference tests using catalysts containing individual metals (Pd, Ni and Co) were also performed to investigate the effect of the bimetallic system on the catalytic behavior in the SRM reactions. The bimetallic system remarkably improves the hydrogen selectivity, methanol conversion and stability of the catalyst. The results are consistent with a synergistic behavior for the Pd-Ni-bimetallic system. The performance, durability and thermal stability of the Pd-Ni/MCM-41 and Pd-Co/MCM-41 suggest that these materials may be promising catalysts for hydrogen production from biofuels. A part of this work for synthesis and characterization of Pd-Ni-MCM-41 and its activity for SRM reactions has been published (“Development of Mesoporous Silica Encapsulated Pd-Ni Nanocatalyst for Hydrogen Production” in “Production and Purification of Ultraclean

  14. Enhanced antibacterial activity of bimetallic gold-silver core-shell nanoparticles at low silver concentration

    Science.gov (United States)

    Banerjee, Madhuchanda; Sharma, Shilpa; Chattopadhyay, Arun; Ghosh, Siddhartha Sankar

    2011-12-01

    Herein we report the development of bimetallic Au@Ag core-shell nanoparticles (NPs) where gold nanoparticles (Au NPs) served as the seeds for continuous deposition of silver atoms on its surface. The core-shell structure and morphology were examined by UV-Vis spectroscopy, transmission electron microscopy (TEM), energy dispersive X-ray (EDX) analysis and X-ray diffraction (XRD). The core-shell NPs showed antibacterial activity against both Gram negative (Escherichia coli and Pseudomonas aeruginosa) and Gram positive (Enterococcus faecalis and Pediococcus acidilactici) bacteria at low concentration of silver present in the shell, with more efficacy against Gram negative bacteria. TEM and flow cytometric studies showed that the core-shell NPs attached to the bacterial surface and caused membrane damage leading to cell death. The enhanced antibacterial properties of Au@Ag core-shell NPs was possibly due to the more active silver atoms in the shell surrounding gold core due to high surface free energy of the surface Ag atoms owing to shell thinness in the bimetallic NP structure.Herein we report the development of bimetallic Au@Ag core-shell nanoparticles (NPs) where gold nanoparticles (Au NPs) served as the seeds for continuous deposition of silver atoms on its surface. The core-shell structure and morphology were examined by UV-Vis spectroscopy, transmission electron microscopy (TEM), energy dispersive X-ray (EDX) analysis and X-ray diffraction (XRD). The core-shell NPs showed antibacterial activity against both Gram negative (Escherichia coli and Pseudomonas aeruginosa) and Gram positive (Enterococcus faecalis and Pediococcus acidilactici) bacteria at low concentration of silver present in the shell, with more efficacy against Gram negative bacteria. TEM and flow cytometric studies showed that the core-shell NPs attached to the bacterial surface and caused membrane damage leading to cell death. The enhanced antibacterial properties of Au@Ag core-shell NPs was

  15. Preparation and properties of the SmOx/Rh(100) model surface

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The preparation of SmOx/Rh(100) and CO adsorption on this model surface have been investigated with Auger electron spectroscopy (AES), X-ray photoelectron spectroscopy (XPS) and temperature programmed desorption spectroscopy (TDS). The oxygen adsorption on the SmRh alloy surface leads to the aggregation of Sm on the surface. The thermal treatment of this oxidized surface induces the further agglomeration of SmOx on the Rh(100) surface. Compared with CO TDS on the clean Rh(100) surface, three additional CO desorption peaks can be observed at 176, 331 and 600 K on the SmOx/Rh(100) surface. The CO desorption peak at 176 K may originate from CO adsorbed on SmOx islands, while the appearance of the CO adsorption peaks at 331 and 600 K, depending on the oxidation state of Sm, is attributed to CO species located at the interface of SmOx/Rh(100).

  16. Plasmonic effects of au/ag bimetallic multispiked nanoparticles for photovoltaic applications.

    Science.gov (United States)

    Sharma, Manisha; Pudasaini, Pushpa Raj; Ruiz-Zepeda, Francisco; Vinogradova, Ekaterina; Ayon, Arturo A

    2014-09-10

    In recent years, there has been considerable interest in the use of plasmons, that is, free electron oscillations in conductors, to boost the performance of both organic and inorganic thin film solar cells. This has been driven by the possibility of employing thin active layers in solar cells in order to reduce materials costs, and is enabled by significant advances in fabrication technology. The ability of surface plasmons in metallic nanostructures to guide and confine light in the nanometer scale has opened up new design possibilities for solar cell devices. Here, we report the synthesis and characterization of highly monodisperse, reasonably stable, multipode Au/Ag bimetallic nanostructures using an inorganic additive as a ligand for photovoltaic applications. A promising surface enhanced Raman scattering (SERS) effect has been observed for the synthesized bimetallic Au/Ag multispiked nanoparticles, which compare favorably well with their Au and Ag spherical nanoparticle counterparts. The synthesized plasmonic nanostructures were incorporated on the rear surface of an ultrathin planar c-silicon/organic polymer hybrid solar cell, and the overall effect on photovoltaic performance was investigated. A promising enhancement in solar cell performance parameters, including both the open circuit voltage (VOC) and short circuit current density (JSC), has been observed by employing the aforementioned bimetallic multispiked nanoparticles on the rear surface of solar cell devices. A power conversion efficiency (PCE) value as high as 7.70% has been measured in a hybrid device with Au/Ag multispiked nanoparticles on the rear surface of an ultrathin, crystalline silicon (c-Si) membrane (∼ 12 μm). This value compares well to the measured PCE value of 6.72% for a similar device without nanoparticles. The experimental observations support the hope for a sizable PCE increase, due to plasmon effects, in thin-film, c-Si solar cells in the near future.

  17. A photoactive bimetallic framework for direct aminoformylation of nitroarenes

    Data.gov (United States)

    U.S. Environmental Protection Agency — A bimetallic catalyst, AgPd@g-C3N4, synthesized by reducing silver and palladium salts over graphitic carbon nitride (g-C3N4), enables the concerted reductive...

  18. Utilization of microfluidic V-junction device to prepare surface itraconazole adsorbed nanospheres.

    OpenAIRE

    Kucuk, I.; Ahmad, Z.; Edirisinghe, M.; Orlu-Gul, M.

    2014-01-01

    Itraconazole is widely used as an anti-fungal drug to treat infections. However its poor aqueous solubility results in low bioavailability. The aim of the present study was to improve the drug release profile by preparing surface itraconazole adsorbed polymethylsilsesquioxane (PMSQ) nanospheres using a V-junction microfluidic (VJM) device. In order to generate nanospheres with rough surface, the process flow rate of Perfluorohexane (PFH) was set between 50 and 300 μl min(-1) while the flow ra...

  19. Spatially selective surface platforms for binding fibrinogen prepared by particle lithography with organosilanes

    OpenAIRE

    Englade-Franklin, Lauren E.; Saner, ChaMarra K.; Garno, Jayne C.

    2013-01-01

    We introduce an approach based on particle lithography to prepare spatially selective surface platforms of organosilanes that are suitable for nanoscale studies of protein binding. Particle lithography was applied for patterning fibrinogen, a plasma protein that has a major role in the clotting cascade for blood coagulation and wound healing. Surface nanopatterns of mercaptosilanes were designed as sites for the attachment of fibrinogen within a protein-resistant matrix of 2-[methoxy(polyethy...

  20. A first-principles study of Pt–Ni bimetallic cluster adsorption on the anatase TiO{sub 2} (1 0 1) surface: Probing electron effect of Ni in TiO{sub 2} (1 0 1)-bimetallic cluster (Pt–Ni) on the adsorption and dissociation of methanol

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Feila, E-mail: liufeila@u.washington.edu [College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044 (China); Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195 (United States); Xiao, Peng, E-mail: xiaopeng@cqu.edu.cn [College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044 (China); Uchaker, Evan, E-mail: uchaker@u.washington.edu [Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195 (United States); He, Huichao, E-mail: hehuichao985@gmail.com [College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044 (China); Zhou, Ming, E-mail: Zhoumingcqu2007@163.com [College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044 (China); Zhou, Xin, E-mail: zhoux@hit.edu.cn [State Key Laboratory of Urban Water Resource and Environment, Institute of Theoretical and Simulation Chemistry, Academy of Fundamental and Interdisciplinary Sciences, Harbin Institute of Technology, Harbin 150080 (China); Zhang, Yunhuai, E-mail: xp2031@163.com [College of Chemistry and Chemical Engineering, Chongqing University, Chongqing 400044 (China)

    2014-10-01

    Graphical abstract: - Highlights: • Condensed Fukui function is used to predict the regioselectivity of clusters. • Pt–Ni alloy and TiO{sub 2} can effectively oxidize methanol compared with pure Pt. • The methanol dehydrogenation over Pt{sub 3}Ni/TiO{sub 2} is an optimal reaction pathway. • The alloying of Ni can effectively alleviate CO poisoning. - Abstract: A density functional theory (DFT) based method in conjunction with the projector augmented wave and pseudopotential methods have been applied to investigate the adsorption of Pt{sub 4} and Pt{sub 3}Ni on the anatase TiO{sub 2} (1 0 1) surface. Two stable Pt{sub 3}Ni adsorptions with considerable adsorption energies on the anatase TiO{sub 2} (1 0 1) surface were identified. Analysis of the partial density (PDOS) of states and Bader charge suggest that the electronic structure of Pt is modified by Ni due to the electron transfer from Ni to Pt atoms in the Pt{sub 3}Ni clusters. The 2cO (3cO)-PtNi-5cTi conformation of the adsorbed Pt{sub 3}Ni on the anatase TiO{sub 2} (1 0 1) surface provides a more feasible model for electron injection through the Pt{sub 3}Ni/TiO{sub 2} interface. The reactivity of Pt{sub 3}Ni/TiO{sub 2} is superior to Pt{sub 4}/TiO{sub 2} and effectively manifests itself in the eased decomposition of O-H bonds derived by methanol and alleviative CO adsorption.

  1. Bimetallic oxamato complexes synthesized into mesoporous matrix as precursor to tunable nanosized oxide

    Energy Technology Data Exchange (ETDEWEB)

    Kalinke, Lucas H.G. [Instituto de Química, Universidade Federal de Goiás—UFG, Goiânia, GO 74001-970 (Brazil); Instituto Federal de Goiás—IFG, Anápolis, GO (Brazil); Stumpf, Humberto O. [Departamento de Química, Instituto de Ciências Exatas, Universidade Federal de Minas Gerais—UFMG, Belo Horizonte, MG (Brazil); Mazali, Italo O. [Instituto de Química, Universidade Estadual de Campinas—UNICAMP, Campinas, SP (Brazil); Cangussu, Danielle, E-mail: danielle_cangussu@ufg.br [Instituto de Química, Universidade Federal de Goiás—UFG, Goiânia, GO 74001-970 (Brazil)

    2015-10-15

    Highlights: • The bimetallic oxamato complexes as single-source precursor. • We prepared into a porous silica glass tunable nanosized oxide powders. • X-ray diffraction shows the formation of CeO{sub 2}/CuO and spinel cobaltite. • The different number of IDC allows control of the nanoparticle size. - Abstract: The bimetallic complexes were employed to prepare into a porous silica glass tunable nanosized oxide powders through the single source precursor (SSP) method. These materials were prepared by first anchoring of [Cu(opba)]{sup 2−} [opba = ortho-phenylenebis(oxamato)], second by reaction in situ with second metal [Co(II) or Ce(III)] and followed by a thermal treatment. The different number of impregnation–decomposition cycles (IDC) allows control of the nanoparticle size. X-ray diffraction shows the formation of mixture CeO{sub 2}–CuO and spinel copper cobaltite. Raman spectroscopy confirmed the formation of such phases. Transmission electron microscopy images revealed that spinel cobaltite particles (8 IDC) present a mean size of about 9 nm, whereas for the CeO{sub 2}–CuO phase the particle diameters are 4 nm (2 IDC) and 8 nm (6 IDC). For CeO{sub 2}–CuO the diffuse reflectance spectroscopy indicates a consistent red shift in band gap from 3.41 to 2.87 eV with increasing of particle size due to quantum confinement effect.

  2. Evaluation of Peel Ply Surface Preparation of Composite Surfaces for Secondary Bonding

    Science.gov (United States)

    2013-09-01

    15 epoxy resin (Applied Poleramic Inc., Benicia, CA) were prepared by the Vacuum Assisted Resin Transfer Molding ( VARTM ) process. Two methods were...viscosity two-phase toughened epoxy resin matrix designed for VARTM processes [8]. The rheological properties of SC-15 have previously been...material system fabricated by the VARTM process ranges between 49 - 52 % with a typical void volume of ~ 1 %, also previously established. Nominal cured

  3. Ordered macroporous bimetallic nanostructures: design, characterization, and applications.

    Science.gov (United States)

    Lu, Lehui; Eychmüller, Alexander

    2008-02-01

    Ordered porous metal nanomaterials have current and future potential applications, for example, as catalysts, as photonic crystals, as sensors, as porous electrodes, as substrates for surface-enhanced Raman scattering (SERS), in separation technology, and in other emerging nanotechnologies. Methods for creating such materials are commonly characterized as "templating", a technique that involves first the creation of a sacrificial template with a specific porous structure, followed by the filling of these pores with desired metal materials and finally the removal of the starting template, leaving behind a metal replica of the original template. From the viewpoint of practical applications, ordered metal nanostructures with hierarchical porosity, namely, macropores in combination with micropores or mesopores, are of particular interest because macropores allow large guest molecules to access and an efficient mass transport through the porous structures is enabled while the micropores or mesopores enhance the selectivity and the surface area of the metal nanostructures. For this objective, colloidal crystals (or artificial opals) consisting of three-dimensional (3D) long-range ordered arrays of silica or polymer microspheres are ideal starting templates. However, with respect to the colloidal crystal templating strategies for production of ordered porous metal nanostructures, there are two challenging questions for materials scientists: (1) how to uniformly and controllably fill the interstitial space of the colloidal crystal templates and (2) how to generate ordered composite metal nanostructures with hierarchical porosity. This Account reports on recent work in the development and applications of ordered macroporous bimetallic nanostructures in our laboratories. A series of strategies have been explored to address the challenges in colloidal crystal template techniques. By rationally tailoring experimental parameters, we could readily and selectively design

  4. Thin-film preparation by back-surface irradiation pulsed laser deposition using metal powder targets

    Science.gov (United States)

    Kawasaki, Hiroharu; Ohshima, Tamiko; Yagyu, Yoshihito; Ihara, Takeshi; Yamauchi, Makiko; Suda, Yoshiaki

    2017-01-01

    Several kinds of functional thin films were deposited using a new thin-film preparation method named the back-surface irradiation pulsed laser deposition (BIPLD) method. In this BIPLD method, powder targets were used as the film source placed on a transparent target holder, and then a visible-wavelength pulsed laser was irradiated from the holder side to the substrate. Using this new method, titanium oxide and boron nitride thin films were deposited on the silicon substrate. Surface scanning electron microscopy (SEM) images suggest that all of the thin films were deposited on the substrate with some large droplets irrespective of the kind of target used. The deposition rate of the films prepared by using this method was calculated from film thickness and deposition time to be much lower than that of the films prepared by conventional PLD. X-ray diffraction (XRD) measurement results suggest that rutile and anatase TiO2 crystal peaks were formed for the films prepared using the TiO2 rutile powder target. Crystal peaks of hexagonal boron nitride were observed for the films prepared using the boron nitride powder target. The crystallinity of the prepared films was changed by annealing after deposition.

  5. Preparing Al-Mg Substrate for Thermal Spraying: Evaluation of Surface State After Different Pretreatments

    Science.gov (United States)

    Lukauskaitė, R.; Valiulis, A. V.; Černašėjus, O.; Škamat, J.; Rębiś, J. A.

    2016-08-01

    The article deals with the pretreatment technique for preparing the surface of aluminum alloy EN AW 5754 before thermal spray. The surface after different pretreatments, including degreasing with acetone, chemical etching with acidic and alkali solutions, grit-blasting, cathodic cleaning, and some combinations of these techniques, has been studied. The investigation of pre-treated surfaces covered the topographical study (using scanning electron microscopy, atomic force microscopy, and 3D profilometry), the chemical analysis by x-ray photoelectron spectroscopy, the evaluation of surface wettability (sessile drop method), and the assessment of surface free energy. Compared with all the techniques used in present work, the cathodic cleaning and its combination with grit-blasting provide the most preferable chemistry of the surface. Due to the absence of hydroxides at the surface and, possible, due to the diffusion of magnesium to the surface of substrate, the surface wettability and the surface free energy have been significantly improved. No direct correlation between the surface topography and the surface wettability has been established.

  6. Preparation of Nanoelectrode Ensembles by Assembly of Nano- Silver Colloid on Gold Surface

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A novel method for preparing silver nanoelectrode ensembles (SNEEs) and gold nanoelectrode ensembles (GNEEs) has been developed. Silver colloid particles were first absorbed to the gold electrode surface to form a monolayer silver colloid. N-hexadecyl mercaptan was then assembled on the electrode to form a thiol monolayer on which hydrophilic ions cannot be transfered. The SNEEs was prepared by removing thiol from silver colloid surface through applying an AC voltage with increasing frequency at 0.20 V (vs. SCE). Finally, GNEEs was obtained by immersing a SNEEs into 6 mol/L HNO3 to remove the silver colloid particles. By comparison with other methods such as template method etc., this method enjoys some advantages of lower resistance, same diameter, easy preparation, controllable size and density.

  7. Preparation of Nanoelectrode Ensembles by Assembly of Nano—Silver Colloid on Gold Surface

    Institute of Scientific and Technical Information of China (English)

    GangXIA; XiaoYaHU; 等

    2002-01-01

    A novel method for preparing silver nanoelectrode ensembles(SNEEs) and gold nanoelectrode ensembles (GNEEs) has been developed. Silver colloid particles were first absorbed to the gold electrode surface to form a monolayer silver colloid. N-hexadecyl nercaptan was then assembled on the electrode to form a thoil monolayer on which hydrophilic ions cannot be transfered. The SNEEs was prepared by removing thiol from silver colloid surface through applying and AC voltage with increasing frequency at 0.20V(vs.SCE). Finally,GNEEs was obtained by immersing a SNEEs into 6 mol/L HNO3 to remove the silver colloid particles. By comparison with other methods such as template method ect., this method enjoys some advantages of lower resistance, same diameter,easy preparation,controllable size and density.

  8. On the role of reactant transport and (surface) alloy formation for the CO tolerance of carbon supported PtRu polymer electrolyte fuel cell catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Kaiser, J.; Colmenares, L.; Jusys, Z.; Behm, R.J. [Abt. Oberflaechenchemie und Katalyse, Universitaet Ulm (Germany); Moertel, R.; Boennemann, H. [Max-Planck-Institut fuer Kohlenforschung, Muelheim a.d. Ruhr (Germany); Koehl, G.; Modrow, H.; Hormes, J. [Physikalisches Institut, Universitaet Bonn (Germany)

    2006-07-15

    The role of atomic scale intermixing for the electrocatalytic activity of bimetallic PtRu anode catalysts in reformate operated polymer electrolyte fuel cells (PEFC) was investigated, exploiting the specific properties of colloid based catalyst synthesis for the selective preparation of alloyed and non-alloyed bimetallic catalysts. Three different carbon supported PtRu catalysts with different degrees of Pt and Ru intermixing, consisting of (i) carbon supported PtRu alloy particles (PtRu/C), (ii) Pt and Ru particles co-deposited on the same carbon support (Pt+Ru/C), and (iii) a mixture of carbon supported Pt and carbon supported Ru (Pt/C+Ru/C) as well as the respective monometallic Pt/C and Ru/C catalysts were prepared and characterized by electron microscopy (TEM), X-ray absorption spectroscopy, and CO stripping. Their performance as PEFC anode catalysts was evaluated by oxidation of a H{sub 2}/2%CO gas mixture (simulated reformate) under fuel cell relevant conditions (elevated temperature, continuous reaction and controlled reactant transport) in a rotating disk electrode (RDE) set-up. The CO tolerance and H{sub 2} oxidation activity of the three catalysts is comparable and distinctly different from that of the monometallic catalysts. The results indicate significant transport of the reactants, CO{sub ad} and/or OH{sub ad}, between Pt and Ru surface areas and particles for all three catalysts, with only subtle differences from the alloy catalyst to the physical mixture. The high activity and CO tolerance of the bimetallic catalysts, through the formation of bimetallic surfaces, is explained, e.g., by contact formation in nanoparticle agglomerates or by material transport and subsequent surface decoration/surface alloy formation during catalyst preparation, conditioning, and operation. The instability and mobility of the catalysts under these conditions closely resembles concepts in gas phase catalysis. (Abstract Copyright [2006], Wiley Periodicals, Inc.)

  9. Preparation and Characterization of Porous Yttrium Oxide Powders with High Specific Surface Area

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The porous cubic yttrium oxides with high specific surface area were prepared by the explosive decomposition of yttrium nitrate and its complex formed with methyl salicylate. The specific surface area and properties of powders synthesized at various temperatures were characterized using BET, X-ray diffraction (XRD), infrared spectra (IR), and scanning electron microscopy (SEM). The results indicate that the highest specific surface area is found to be 65.37 m2*g-1 at the calcination temperature of 600 ℃, and then decreases to 20.33 m2*g-1 with the calcination temperature rising from 600 to 900 ℃. The powders show strong surface activity for adsorping water and carbon dioxide in air, which also decreases with the rising calcination temperature. The drop both on the surface area and surface activity of samples at higher temperatures may be due to pore-narrowing(sintering) effects.

  10. Spatially selective surface platforms for binding fibrinogen prepared by particle lithography with organosilanes.

    Science.gov (United States)

    Englade-Franklin, Lauren E; Saner, Chamarra K; Garno, Jayne C

    2013-06-06

    We introduce an approach based on particle lithography to prepare spatially selective surface platforms of organosilanes that are suitable for nanoscale studies of protein binding. Particle lithography was applied for patterning fibrinogen, a plasma protein that has a major role in the clotting cascade for blood coagulation and wound healing. Surface nanopatterns of mercaptosilanes were designed as sites for the attachment of fibrinogen within a protein-resistant matrix of 2-[methoxy(polyethyleneoxy)propyl] trichlorosilane (PEG-silane). Preparing site-selective surfaces was problematic in our studies, because of the self-reactive properties of PEG-organosilanes. Certain organosilanes presenting hydroxyl head groups will cross react to form mixed surface multi-layers. We developed a clever strategy with particle lithography using masks of silica mesospheres to protect small, discrete regions of the surface from cross reactions. Images acquired with atomic force microscopy (AFM) disclose that fibrinogen attached primarily to the surface areas presenting thiol head groups, which were surrounded by PEG-silane. The activity for binding anti-fibrinogen was further evaluated using ex situ AFM studies, confirming that after immobilization the fibrinogen nanopatterns retained capacity for binding immunoglobulin G. Studies with AFM provide advantages of achieving nanoscale resolution for detecting surface changes during steps of biochemical surface reactions, without requiring chemical modification of proteins or fluorescent labels.

  11. Gyroscopic behavior exhibited by the optical Kerr effect in bimetallic Au-Pt nanoparticles suspended in ethanol

    Science.gov (United States)

    Fernández-Valdés, D.; Torres-Torres, C.; Martínez-González, C. L.; Trejo-Valdez, M.; Hernández-Gómez, L. H.; Torres-Martínez, R.

    2016-07-01

    The modification in the third-order nonlinear optical response exhibited by rotating bimetallic Au-Pt nanoparticles in an ethanol solution was analyzed. The samples were prepared by a sol-gel processing route. The anisotropy associated to the elemental composition of the nanoparticles was confirmed by high-resolution transmission electron microscopy and energy-dispersive X-ray spectroscopy measurements. The size of the nanoparticles varies in the range from 9 to 13 nm, with an average size of 11 nm. Changes in the spatial orientation of the nanomaterials automatically generated a variation in their plasmonic response evaluated by UV-Vis spectroscopy. A two-wave mixing experiment was conducted to explore an induced birefringence at 532 nm wavelength with nanosecond pulses interacting with the samples. A strong optical Kerr effect was identified to be the main responsible effect for the third-order nonlinear optical phenomenon exhibited by the nanoparticles. It was estimated that the rotation of inhomogeneous nanostructures can provide a remarkable change in the participation of different surface plasmon resonances, if they correspond to multimetallic nanoparticles. Potential applications for developing low-dimensional gyroscopic systems can be contemplated.

  12. Bimetallic NiCo functional graphene: an efficient catalyst for hydrogen-storage properties of MgH₂.

    Science.gov (United States)

    Wang, Ying; Liu, Guang; An, Cuihua; Li, Li; Qiu, Fangyuan; Wang, Yijing; Jiao, Lifang; Yuan, Huatang

    2014-09-01

    Bimetallic NiCo functional graphene (NiCo/rGO) was synthesized by a facile one-pot method. During the coreduction process, the as-synthesized ultrafine NiCo nanoparticles (NPs), with a typical size of 4-6 nm, were uniformly anchored onto the surface of reduced graphene oxide (rGO). The NiCo bimetal-supported graphene was found to be more efficient than their single metals. Synergetic catalysis of NiCo NPs and rGO was confirmed, which can significantly improve the hydrogen-storage properties of MgH2. The apparent activation energy (E(a)) of the MgH2-NiCo/rGO sample decreases to 105 kJ mol(-1), which is 40.7% lower than that of pure MgH2. More importantly, the as-prepared MgH2-NiCo/rGO sample can absorb 5.5 and 6.1 wt% hydrogen within 100 and 350 s, respectively, at 300 °C under 0.9 MPa H2 pressure. Further cyclic kinetics investigation indicates that MgH2-NiCo/rGO nanocomposites have excellent cycle stability.

  13. Electrochemical characterization of platinum-ruthenium nanoparticles prepared by water-in-oil microemulsion

    Energy Technology Data Exchange (ETDEWEB)

    Solla-Gullon, J.; Vidal-Iglesias, F.J.; Montiel, V.; Aldaz, A. [Universidad de Alicante (Spain). Instituto Universitario de Electroquimica, Departamento de Quimica-Fisica

    2004-11-01

    The synthesis, physical characterization, decontamination and some electrocatalytic properties of PtRu nanoparticles prepared using the microemulsion method are reported. The nanoparticles are synthesized by reduction with sodium borohydride of H{sub 2}PtCl{sub 6} and RuCl{sub 3} in a water-in-oil microemulsion of water/polyethylenglycol-dodecylether (BRIJ(Registered Trademark) 30)/n-heptane. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and energy dispersive analysis by X-rays (EDAX) experiments were carried out to characterize the single and bimetallic nanoparticles obtained. Cyclic voltammograms (CV) of clean nanoparticles were obtained after a controlled decontamination procedure of their surfaces. CO adsorption-oxidation and methanol electrooxidation were tested as test reactions to check the electrocatalytic behaviour of the bimetallic nanoparticles. Pt{sub 80}Ru{sub 20} (nominal atomic composition) nanoparticles are the best electrocatalyst for both CO{sub ad} and methanol oxidation. All these results show that the microemulsion method can be used to produce bimetallic nanoparticles in a very easy way. The method can be very easily scaled-up for industrial use. (author)

  14. Preparation and recognition performance of cytisine alkaloid-imprinted material prepared using novel surface molecular imprinting technique.

    Science.gov (United States)

    Gao, Baojiao; Niu, Qinyuan; Du, Ruikui

    2010-05-01

    Methacrylic acid was first graft-polymerized on the surfaces of micron-sized silica gel particles in the manner of "grafting from" using 3-methacryloxypropyl trimethoxysilane as an intermedia, obtaining the grafted particle polymethacrylic acid PMAA/SiO(2). By adopting the novel surface-molecular imprinting technique put forward by us, cytisine molecule-imprinted material MIP-PMAA/SiO(2) was prepared with ethylene glycol diglycidyl ether as crosslinking agent. The binding characteristics of MIP-PMAA/SiO(2) towards cytisine was investigated in depth with both batch and column methods and using matrine and oxymatrine as two contrast alkaloids, which with cytisine coexist in sophora alopecuroides and their chemical structure is similar to cytisine to a certain extent. The experimental results show that the surface-imprinted material MIP-PMAA/SiO(2) has excellent binding affinity for cytisine (20.1 g/100 g of binding capacity), and it is more important that MIP-PMAA/SiO(2) has very high recognition selectivity for cytisine in relation to the two contrast alkaloids. The selectivity coefficients of the grafted particles PMAA/SiO(2) (non-imprinted material) for cytosine in relation to matrine and oxymatrine are only 1.03 and 1.06, respectively, displaying no recognition selectivity for cytisine. However, after imprinting, the selectivity coefficient of MIP-PMAA/SiO(2) for cytisine in respect to matrine and oxymatrine are remarkably enhanced to 12.08 and 15.05, respectively.

  15. The influence of surface preparation on the absorption coefficient of laser radiation

    Science.gov (United States)

    Kurp, Piotr; Mucha, Zygmunt; Mulczyk, Krystian; Gradoń, Ryszard; Trela, Paweł

    2016-12-01

    The absorption coefficient of the surface of a workpiece is of importance in laser treatment, particularly in the treatment where the temperature of an element must be strictly controlled. Laser surface treatment (such as hardening, metallic glazing) and laser forming can be primarily included in this type of technology. In another case, surface temperature must be precisely controlled, especially if structural changes are to be avoided. There are a number of ways to increase the absorption coefficient of the surface of an element. Since the laser forming is the research subject of the authors of the presented paper, it was necessary to determine the absorption coefficient for the different surfaces preparation of workpieces. Raw surface, oxidized surface, sandblasted surface, black enamel covered surface and waterglass covered surface were examined, respectively. The experiment was performed using a CO2 laser with a head for a surface treatment which generates a rectangular beam of dimensions 2x20 mm, and the samples were made of X5CrNi18-10 stainless steel.

  16. Bimetallic Microswimmers Speed Up in Confining Channels

    Science.gov (United States)

    Liu, Chang; Zhou, Chao; Wang, Wei; Zhang, H. P.

    2016-11-01

    Synthetic microswimmers are envisioned to be useful in numerous applications, many of which occur in tightly confined spaces. It is therefore important to understand how confinement influences swimmer dynamics. Here we study the motility of bimetallic microswimmers in linear and curved channels. Our experiments show swimmer velocities increase, up to 5 times, with the degree of confinement, and the relative velocity increase depends weakly on the fuel concentration and ionic strength in solution. Experimental results are reproduced in a numerical model which attributes the swimmer velocity increase to electrostatic and electrohydrodynamic boundary effects. Our work not only helps to elucidate the confinement effect of phoretic swimmers, but also suggests that spatial confinement may be used as an effective control method for them.

  17. Termination of single-crystal B i2S e3 surfaces prepared by various methods

    Science.gov (United States)

    Zhou, Weimin; Zhu, Haoshan; Yarmoff, Jory A.

    2016-11-01

    Bismuth Selenide (B i2S e3) is a topological insulator with a two-dimensional layered structure that enables clean and well-ordered surfaces to be prepared by cleaving. Although some studies have demonstrated that the cleaved surface is terminated with Se, as expected from the bulk crystal structure, other reports have indicated either a Bi- or mixed-termination. Low-energy ion scattering (LEIS), low energy electron diffraction (LEED) and x-ray photoelectron spectroscopy (XPS) are used here to compare surfaces prepared by ex situ cleaving, in situ cleaving, and ion bombardment and annealing (IBA) in ultrahigh vacuum (UHV). Surfaces prepared by in situ cleaving and IBA are well ordered and Se-terminated. Ex situ cleaved samples could be either Se-terminated or Bi-rich, are less well ordered and have adsorbed contaminants. This suggests that a chemical reaction involving atmospheric contaminants, which may preferentially adsorb at surface defects, could contribute to the nonreproducibility of the termination.

  18. Preparation, Surface and Pore Structure of High Surface Area Activated Carbon Fibers from Bamboo by Steam Activation

    Directory of Open Access Journals (Sweden)

    Xiaojun Ma

    2014-06-01

    Full Text Available High surface area activated carbon fibers (ACF have been prepared from bamboo by steam activation after liquefaction and curing. The influences of activation temperature on the microstructure, surface area and porosity were investigated. The results showed that ACF from bamboo at 850 °C have the maximum iodine and methylene blue adsorption values. Aside from the graphitic carbon, phenolic and carbonyl groups were the predominant functions on the surface of activated carbon fiber from bamboo. The prepared ACF from bamboo were found to be mainly type I of isotherm, but the mesoporosity presented an increasing trend after 700 °C. The surface area and micropore volume of samples, which were determined by application of the Brunauer-Emmett-Teller (BET and t-plot methods, were as high as 2024 m2/g and 0.569 cm3/g, respectively. It was also found that the higher activation temperature produced the more ordered microcrystalline structure of ACF from bamboo.

  19. Electrocatalysis of fuel cells reaction on Pt and Pt-bimetallic anode catalysts: A selective review

    Directory of Open Access Journals (Sweden)

    Stamenković Vojislav

    2002-01-01

    Full Text Available In this review we selectively summarize recent progress, primarily from our laboratory, in the development of interrelationships between the kinetics of the fuel cells reactions and the structure/composition of anode catalysts. The focus is placed on two types of metallic surfaces: platinum single crystals and bimetallic surfaces based on Pt. In the first part it was illustrated that the hydcogen reaction is structure sensitive process, with Pt(110 being an order of magnitude more active than either of the atomically "flatter" (100 and (111 surfaces. The hydrogen reaction on Pt(hkl modified by pseudomorphic Pd (submonolayers shows the "volcano-like" behavior, having the maximum rate on Pt(111 modified by 1 ML of Pd. The Pt(111-Pd system is used to demonstrate how the energetics of intermediates formed in the hydrogen reaction is affected by interfacial bonding and energetic constraints produced between pseudomorphic Pd films and the Pt(111 substrate. In the second part it was shown that the oxidation of Ha in the presence of CO occurs concurrently with CO oxidation on Pt and Pt bimetallic surfaces. The Pt-Ru system is used to demonstrate that both the bifunctional effect and the ligand effect contribute to the influence of Ru on the CO oxidation rate and for Hz oxidation process in the presence of CO. The knowledge is then used to create the real-life catalyst with the catalytic activities which are, to the greatest extend possible similar to the tailor-made surface.

  20. Preparation and characterization of 3-(triethoxysilyl) propyl isocyanate self-assembled monolayer on surface of chip

    Institute of Scientific and Technical Information of China (English)

    XIE Yao; GENG LiNa; QU Feng; LUO AiQin; QU Feng; DENG YuLin

    2009-01-01

    Monolayer of 3-(triethoxysilyl) propyl isocyanate was prepared on the slide by self-assembled tech-nique. X-ray photoelectron spectroscopy (XPS) was employed to analyze the elementary composition of the film. Contact angle of distilled water was measured to characterize the surface state. It was shown that 3-(triethoxysilyl) propyl isocyanate had been successfully assembled on the slide. The in-crease of contact angle to 80 demonstrated that the hydrophobicity of the surface of chip was in-creased significantly. Moreover, further self-assembly of bovine serum albumin (BSA) on 3-(trietho-xysilyl) propyl isocyanate was also carried out with the advantages such as simple and convenient preparation. Therefore, the potential of broader applications in the modification of micro-channel in the μ-TAS system, the immobilization of protein or peptide and the surface modification of materials are all expectative.

  1. Surface treatment of nickel substrate for the preparation of BSCCO film through sol-gel method

    Energy Technology Data Exchange (ETDEWEB)

    Yang Huazhe, E-mail: hzyang@mail.cmu.edu.cn [Department of Biophysics, College of Basic Medical Science, China Medical University, Shenyang 110001 (China); Yu Xiaoming [Institute of Materials Physics and Chemistry, School of Sciences, Northeastern University, Shenyang 110819 (China); Ji Yang [Stomatology Department of the General Hospital of Shenyang Military Area Command, Shenyang, 110840 (China); Qi Yang, E-mail: qiyang@imp.neu.edu.cn [Institute of Materials Physics and Chemistry, School of Sciences, Northeastern University, Shenyang 110819 (China)

    2012-03-15

    A modified degreasing-oxidization process was devised and settled to treat the surface of nickel (Ni) substrates, and BSCCO films were prepared on the treated NiO/Ni substrates by sol-gel method. X-ray diffraction (XRD) and optical microscopy were adopted to clarify the function of different treatment on phase formation and wettability of NiO/Ni substrates. Differential thermal analysis and thermal gravimetry analysis were adopted to confirm the desirable heat treatment process. XRD and scanning electron microscopy were adopted to investigate the phase constituent and surface morphology of BSCCO films. Results demonstrate that both the surface wettability of the substrate to sol and the lattice matching between the substrate and BSCCO can be improved through the modified treatment, which are favorable for the preparation of BSCCO films.

  2. All-(111) surface silicon nanowire field effect transistor devices: Effects of surface preparations

    NARCIS (Netherlands)

    Masood, Muhammad Nasir; Carlen, Edwin T.; Berg, van den Albert

    2014-01-01

    Etching/hydrogen termination of All-(111) surface silicon nanowire field effect (SiNW-FET) devices developed by conventional photolithography and plane dependent wet etchings is studied with X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), atomic force microscopy (AFM) and

  3. Preparation and Biocompatible Surface Modification of Redox Altered Cerium Oxide Nanoparticle Promising for Nanobiology and Medicine

    KAUST Repository

    Nanda, Himansu

    2016-11-03

    The biocompatible surface modification of metal oxide nanoparticles via surface functionalization technique has been used as an important tool in nanotechnology and medicine. In this report, we have prepared aqueous dispersible, trivalent metal ion (samarium)-doped cerium oxide nanoparticles (SmCNPs) as model redox altered CNPs of biological relevance. SmCNP surface modified with hydrophilic biocompatible (6-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-hexyl) triethoxysilane (MEEETES) were prepared using ammonia-induced ethylene glycol-assisted precipitation method and were characterized using a variety of complementary characterization techniques. The chemical interaction of functional moieties with the surface of doped nanoparticle was studied using powerful 13C cross polarization magic angle sample spinning nuclear magnetic resonance spectroscopy. The results demonstrated the production of the extremely small size MEEETES surface modified doped nanoparticles with significant reduction in aggregation compared to their unmodified state. Moreover, the functional moieties had strong chemical interaction with the surface of the doped nanoparticles. The biocompatible surface modification using MEEETES should also be extended to several other transition metal ion doped and co-doped CNPs for the production of aqueous dispersible redox altered CNPs that are promising for nanobiology and medicine.

  4. Preparation and Biocompatible Surface Modification of Redox Altered Cerium Oxide Nanoparticle Promising for Nanobiology and Medicine

    Directory of Open Access Journals (Sweden)

    Himansu Sekhar Nanda

    2016-11-01

    Full Text Available The biocompatible surface modification of metal oxide nanoparticles via surface functionalization technique has been used as an important tool in nanotechnology and medicine. In this report, we have prepared aqueous dispersible, trivalent metal ion (samarium-doped cerium oxide nanoparticles (SmCNPs as model redox altered CNPs of biological relevance. SmCNP surface modified with hydrophilic biocompatible (6-{2-[2-(2-methoxy-ethoxy-ethoxy]-ethoxy}-hexyl triethoxysilane (MEEETES were prepared using ammonia-induced ethylene glycol-assisted precipitation method and were characterized using a variety of complementary characterization techniques. The chemical interaction of functional moieties with the surface of doped nanoparticle was studied using powerful 13C cross polarization magic angle sample spinning nuclear magnetic resonance spectroscopy. The results demonstrated the production of the extremely small size MEEETES surface modified doped nanoparticles with significant reduction in aggregation compared to their unmodified state. Moreover, the functional moieties had strong chemical interaction with the surface of the doped nanoparticles. The biocompatible surface modification using MEEETES should also be extended to several other transition metal ion doped and co-doped CNPs for the production of aqueous dispersible redox altered CNPs that are promising for nanobiology and medicine.

  5. Facile fabrication of Pt-Ag bimetallic nanoparticles decorated reduced graphene oxide for highly sensitive non-enzymatic hydrogen peroxide sensing.

    Science.gov (United States)

    Zhang, Cong; Zhang, Yanyan; Du, Xin; Chen, Yuan; Dong, Wenhao; Han, Bingkai; Chen, Qiang

    2016-10-01

    A new electrocatalyst, Pt-Ag bimetallic nanoparticles decorated reduced graphene oxide nanocomposite, was successfully synthesized by a facile, eco-friendly and controllable route. The morphological characterization of RGO/Pt-Ag NPs nanocomposite was examined by transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX) analyzer, X-ray diffraction (XRD) spectrum, and Fourier transform infrared spectrum (FT-IR), respectively. And then, the RGO/Pt-Ag NPs nanocomposite was immobilized on the surface of glassy carbon (GC) electrode to fabricate a novel and highly sensitive non-enzymatic hydrogen peroxide sensor. The electrochemical behaviors of the prepared sensor were investigated by cyclic voltammetry and chronoamperometry. The sensor showed excellent performance toward H2O2 with sensitivity as high as 699.6 μA mM(-1)cm(-2) and 402.7 μA mM(-1)cm(-2), wide linear range of 0.005-1.5mM and 1.5-7mM, and low detection limit of 0.04μM (S/N=3). Moreover, the prepared hydrogen peroxide sensor was applied to in real samples with satisfactory results. These excellent results indicate that the prepared RGO/Pt-Ag NPs nanocomposite has broad application prospect in the field of sensors.

  6. Ultrasmooth gold surfaces prepared by chemical mechanical polishing for applications in nanoscience.

    Science.gov (United States)

    Miller, Michael S; Ferrato, Michael-Anthony; Niec, Adrian; Biesinger, Mark C; Carmichael, Tricia Breen

    2014-12-02

    For over 20 years, template stripping has been the best method for preparing ultrasmooth metal surfaces for studies of nanostructures. However, the organic adhesives used in the template stripping method are incompatible with many solvents, limiting the conditions that may subsequently be used to prepare samples; in addition, the film areas that can be reliably prepared are typically limited to ∼1 cm(2). In this article, we present chemical-mechanical polishing (CMP) as an adhesive-free, scalable method of preparing ultrasmooth gold surfaces. In this process, a gold film is first deposited by e-beam evaporation onto a 76-mm-diameter silicon wafer. The CMP process removes ∼4 nm of gold from the tops of the grains comprising the gold film to produce an ultrasmooth gold surface supported on the silicon wafer. We measured root-mean-square (RMS) roughness values using atomic force microscopy of 12 randomly sampled 1 μm × 1 μm areas on the surface of the wafer and repeated the process on 5 different CMP wafers. The average RMS roughness was 3.8 ± 0.5 Å, which is comparable to measured values for template-stripped gold (3.7 ± 0.5 Å). We also compared the use of CMP and template-stripped gold as bottom electrical contacts in molecular electronic junctions formed from n-alkanethiolate self-assembled monolayers as a sensitive test bed to detect differences in the topography of the gold surfaces. We demonstrate that these substrates produce statistically indistinguishable values for the tunneling decay coefficient β, which is highly sensitive to the gold surface topography.

  7. Mixed-phase Pd-Pt bimetallic alloy on graphene oxide with high activity for electrocatalytic applications

    Science.gov (United States)

    Khan, Majid; Yousaf, Ammar Bin; Chen, Mingming; Wei, Chengsha; Wu, Xibo; Huang, Ningdong; Qi, Zeming; Li, Liangbin

    2015-05-01

    Bimetallic PdPt alloy nanoparticles on graphene oxide (GO) have been prepared by a simple and facile chemical route, in which the reduction of metal precursors is carried out using CO as a reductant. Structural and morphological characterizations of GO/PdPt composites are performed using X-ray diffraction, X-ray photoelectron spectroscopy analysis and transmission electron microscopy. It is found that PdPt bimetallic nanoparticles are successfully synthesized and uniformly attached on the graphene sheets. The electrocatalytic and electrochemical properties of GO/PdPt composites including methanol oxidation reaction (MOR), oxygen reduction reaction (ORR) and methanol tolerant oxygen reduction reaction (MTORR) are studied in HClO4 aqueous solution. A significant improvement in the electrocatalytic activities is observed by increasing the atomic ratio of Pt in PdPt bimetallic alloys compared to the freestanding Pd nanoparticles on GO. The prepared GO/PdPt composites with an (Pd:Pt) atomic ratio of 40:60 exhibits higher methanol oxidation activity, higher specific ORR activity and better tolerance to CO poisoning. The results can be attributed to the collective effects of the PdPt nanoparticles and the enhanced electron transfer of graphene.

  8. Breakdown of the Hume-Rothery Rules in Sub-Nanometer-Sized Ta-Containing Bimetallic Small Clusters

    Science.gov (United States)

    Miyajima, Ken; Fukushima, Naoya; Himeno, Hidenori; Yamada, Akira; Mafuné, Fumitaka

    2009-11-01

    The Hume-Rothery rules are empirical rules to predict the solid solubility of metals. We examined whether the rules hold for sub-nanometer-sized small particles. We prepared bimetallic cluster ions in the gas phase by a double laser ablation technique. Taking advantage of the magic compositions of the bimetallic cluster ions relating to the distinguished stabilities, the coalescence or the segregation of Ta and another element in the sub-nanometer-sized clusters was discussed. It was found that W, Nb, and Mo readily coalesce with Ta, while Ag, Al, Au, Co, Cu, Fe, Hf, Ni, Pt, Ti, and V are segregated from Ta. On the basis of these results, we concluded that the Hume-Rothery rules do not hold for sub-nanometer-sized particles.

  9. Shaped Ir-Ni bimetallic nanoparticles for minimizing Ir utilization in oxygen evolution reaction.

    Science.gov (United States)

    Lim, Jinkyu; Yang, Sungeun; Kim, Chanyeon; Roh, Chi-Woo; Kwon, Yongwoo; Kim, Yong-Tae; Lee, Hyunjoo

    2016-04-25

    Shaped Ir-Ni bimetallic nanoparticles were synthesized and used for electrocatalytic oxygen evolution reaction (OER). The obtained bimetallic nanoparticles showed significantly enhanced Ir mass activity and durability compared with Ir nanoparticles.

  10. RESOURCE-SAVING TECHNOLOGY FOR HIGH-SPEED HOT EXTRUSION OF BIMETALLIC ROD PARTS

    Directory of Open Access Journals (Sweden)

    I. V. Kachanov

    2016-01-01

    Full Text Available Processes of high-speed shaping changes and especially high-speed hot extrusion create efficient conditions for treatment of weakly plastic and poorly deformable materials which are widely used in tool making facilities. Due to the fact that high-speed stamping provides accurate billets with increased mechanical properties, it can be used as a technological process for manufacturing rod parts of die tooling operating under conditions of increased loads and wear. The purpose of the given paper is to carry out experimental investigations on the possibility to obtain a bimetallic rod tool where structural steel is considered as a basis of the tool and a working cavity is made of high-alloyed tool steel with its saving up to 90 %. A scheme of loading and geometry of conjugated surfaces of the composite billet have been developed in the paper. Technology for obtaining bimetallic rod parts of die tooling with deformation at speed of vд = 70–80 m/s and composite billet temperature of Т = (1150±20 ºС has been experimentally tested with formation of a compound due to plastic flow of two billet parts on contact surface with removal of surface oxide films. Microstructures of the bimetallic compounds obtained with the help of high-speed hot extrusion method for compositions of structural and high-alloy steels have been investigated and their high quality has been proved during the investigations. Dependences of micro-hardness distribution have been established outbound two steel contact plane in the zone of connection that are characterized by a minimum micro-hardness value in the connection joint. Availability of more plastic zone in the contact plane contributes to reduction of residual stresses due to their relaxation in this zone and higher joint strength.

  11. Synthesis and characterization of bimetallic Cu-Ni/ZrO{sub 2} nanocatalysts: H{sub 2} production by oxidative steam reforming of methanol

    Energy Technology Data Exchange (ETDEWEB)

    Perez-Hernandez, R.; Mondragon Galicia, G.; Mendoza Anaya, D.; Palacios, J. [Instituto Nacional de Investigaciones Nucleares; Carretera Mexico-Toluca S/N La Marquesa, Ocoyoacac, Estado de Mexico C.P. 52750 (Mexico); Angeles-Chavez, C. [Programa de Ingenieria Molecular, Instituto Mexicano del Petroleo, Eje Central Lazaro Cardenas, No. 152, C.P. 07730, Mexico D.F. (Mexico); Arenas-Alatorre, J. [Instituto de Fisica-UNAM, Apartado Postal 20-364, C.P. 01000, Mexico D.F. (Mexico)

    2008-09-15

    Cu/ZrO{sub 2}, Ni/ZrO{sub 2} and bimetallic Cu-Ni/ZrO{sub 2} catalysts were prepared by deposition-precipitation method to produce hydrogen by oxidative steam reforming of methanol (OSRM) reaction in the range of 250-360 C. TPR analysis of the Cu-Ni/ZrO{sub 2} catalyst showed that the presence of Cu facilitates the reduction of the Ni at lower temperatures. In addition, this sample showed two reduction peaks, the former peak was attributed to the reduction of the adjacent Cu and Ni atoms which could be forming a bimetallic Cu-rich phase, and the second was assigned to the remaining Ni atoms forming bimetallic Ni-rich nanoparticles. Transmission Electron Microscopy revealed Cu or Ni nanoparticles on the monometallic samples, while bimetallic nanoparticles were identified on the Cu-Ni/ZrO{sub 2} catalyst. On the other hand, Cu-Ni/ZrO{sub 2} catalyst exhibited better catalytic activity than the monometallic samples. The difference between them was related to the Cu-Ni nanoparticles present on the former catalyst, as well as the bifunctional role of the bimetallic phase and the support that improve the catalytic activity. All the catalysts showed the same selectivity toward H{sub 2} at the maximum reaction temperature and it was {proportional_to}60%. The high selectivity toward CO is associated to the presence of the bimetallic Ni-rich nanoparticles, as evidenced by TEM-EDX analysis, since this behavior is similar to the one showed by the monometallic Ni-catalyst. (author)

  12. BIOMIMETIC SURFACE PREPARATION OF INERT POLYMER FILMS VIA GRAFTING LONG MONOALKYL CHAIN PHOSPHATIDYLCHOLINE

    Institute of Scientific and Technical Information of China (English)

    Peng-jun Wan; Dong-sheng Tan; Zheng-sheng Li; Xiao-qing Zhang; Jie-hua Li; Hong Tan

    2012-01-01

    To explore construction of novel mimicking biomembrane on biomaterials surfaces,a new polymerizable phosphatidylcholine containing a long monoalkyl chain ended with acryl group (AASOPC) was designed and synthesized,which was easily derived from the terminal amino group of 9-(2-amino-ethylcarbamoyl)-nonyl-l-phosphatidyl-choline (ASOPC) reacting with acryloyl chloride.The obtained AASOPC was grafted on poly(ethylene terephthalate) (PET) via surface-initiated atom-transfer radical polymerization (SI-ATRP) to form mimicking biomembrane.These modified surface structures of PET were investigated using water contact angle (WAC),X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM).The results indicated that the new mimicking phosphatidylcholine biomembrane could be prepared on inert polymer surfaces by using the acryloyl phosphatidylcholine (AASOPC) via surface-initiated atom transfer radical polymerization (SI-ATRP).

  13. Surface Functionality Features of Porous Silicon Prepared and Treated in Different Conditions

    Directory of Open Access Journals (Sweden)

    Yu. M. Spivak

    2016-01-01

    Full Text Available Hydrophilic layers of porous silicon are prepared by single- or two-step anodization and characterized by evaluating their surface hydrophilicity and contents of functional groups using IR spectroscopy and adsorption of acid-base indicators with different pKa values. The surface functional composition of the synthesized samples is shown to be adjustable depending on the anodization current density. The surface of samples obtained at anodization current density 30 mA/cm2 is predominantly occupied with pKa 2.5 corresponding to ≡Si–OH groups. The increase of current density to 80 mA/cm2 results in the increase of surface functional nonuniformity with the formation of versatile centers, primarily Lewis acidic sites corresponding to Si atoms, as indicated by selective indicator adsorption in agreement with the disappearance of Si–H bonds in IR spectra and overall surface disordering according to SEM and AFM data.

  14. Preparation and characterization of chemical gradient surfaces and their application for the study of cellular interaction phenomena

    NARCIS (Netherlands)

    Ruardy, TG; Schakenraad, JM; vanderMei, HC; Busscher, HJ

    1997-01-01

    Chemical gradient surfaces are surfaces with a gradually changing chemistry along their length which is responsible for a position bound variation in physical properties, most notably, the wettability. In this review, methods to prepare (palladium deposition, diffusion technique, density gradient

  15. Surface engineered nanoparticles for improved surface enhanced Raman scattering applications and method for preparing same

    Science.gov (United States)

    Simmons, Blake A.; Talin, Albert Alec

    2009-11-27

    A method for producing metal nanoparticles that when associated with an analyte material will generate an amplified SERS spectrum when the analyte material is illuminated by a light source and a spectrum is recorded. The method for preparing the metal nanoparticles comprises the steps of (i) forming a water-in-oil microemulsion comprising a bulk oil phase, a dilute water phase, and one or more surfactants, wherein the water phase comprises a transition metal ion; (ii) adding an aqueous solution comprising a mild reducing agent to the water-in-oil microemulsion; (iii) stirring the water-in-oil microemulsion and aqueous solution to initiate a reduction reaction resulting in the formation of a fine precipitate dispersed in the water-in-oil microemulsion; and (iv) separating the precipitate from the water-in-oil microemulsion.

  16. Influential factors of 2-chlorobiphenyl reductive dechlorination by highly dispersed bimetallic nanoparticles

    Directory of Open Access Journals (Sweden)

    Jiang Junrong

    2016-01-01

    Full Text Available Highly dispersed Pd-Fe0 bimetallic nanoparticles were prepared in the presence of 40 kHz ultrasonic irradiation in order to enhance disparity and reactivity, and simultaneously avoid agglomeration. Influential factors of 2-chlorobiphenyl (2-Cl BP reductive dechlorination by highly dispersed Pd-Fe0 nanoparticles were investigated. Experimental results showed that highly dispersed Pd-Fe0 nanoparticles prepared in the in the presence of ultrasound could further improve the dechlorination efficiency of 2-Cl BP, meanwhile the biphenyl (BP formation rates increased obviously and increased from 47.4% (in the absence of ultrasound to 95.3% (in the presence of ultrasound within 300 min. The catalytic reductive dechlorination effciency of 2-Cl BP was dependent on Pd-Fe0 nanoparticles prepared methods, Pd-Fe0 nanoparticles dosage, Pd loading percentage over Fe0 and initial pH values

  17. Temperature variation on root surface with three root-end cavity preparation techniques

    Directory of Open Access Journals (Sweden)

    Bodrumlu Emre

    2013-01-01

    Full Text Available Introduction. Thermal changes can occur on the external root surface when root-end cavity preparation is performed, which may damage periodontal ligament cells and alveolar bone. Objective. The purpose of this study was to evaluate the temperature changes during preparation of the root-end cavities at 1 and 3 mm to the sectioned apical root surfaces when either tungsten carbide round bur, diamond round bur or ultrasonic diamond tip was used. Methods. Root-end resection was performed at 90° to the long axis of the root, 3 mm from the apex. Specimens were randomly divided into three groups of 12 teeth each for three different root-end cavity preparation techniques to be used, i.e. tungsten carbide bur, diamond bur and ultrasonic diamond retro tip. Thermocouples were used to measure temperature changes at 1 mm (T1 and 3 mm (T2 to the cutting plane during the preparations. Results. For T1, the lowest and the highest mean temperature increases of 3.53°C and 4.34°C were recorded for the carbide and diamond burs, respectively. For T2, the lowest and the highest mean temperature increases of 2.62°C and 4.39°C where recorded for the carbide and diamond burs, respectively. The mean temperatures with the ultrasonic tip were 3.68 and 3.04 ºC at T1 and T2 region, respectively. For root-end preparation, the ultrasonic preparation technique took the shortest preparation time (10.25 sec and the diamond bur took the longest time (28.17 sec. Conclusion. Ultrasonic retro tips and burs caused temperature to rise from 2.62° to 4.39°C, and these rises were within safety levels.

  18. Insights into the superhydrophobicity of metallic surfaces prepared by electrodeposition involving spontaneous adsorption of airborne hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Peng; Cao, Ling; Zhao, Wei; Xia, Yue; Huang, Wei; Li, Zelin, E-mail: lizelin@hunnu.edu.cn

    2015-01-01

    Graphical abstract: - Highlights: • Several superhydrophobic metallic surfaces were fabricated by fast electrodeposition. • Both micro/nanostructures and adsorption of airborne hydrocarbons make contributions. • XPS analyses confirm presence of airborne hydrocarbons on these metallic surfaces. • The adsorption of airborne hydrocarbons on the clean metal Au surface was very quick. • UV-O{sub 3} treatment oxidized the hydrocarbons to hydrophilic oxygen-containing organics. - Abstract: Electrochemical fabrication of micro/nanostructured metallic surfaces with superhydrophobicity has recently aroused great attention. However, the origin still remains unclear why smooth hydrophilic metal surfaces become superhydrophobic by making micro/nanostructures without additional surface modifications. In this work, several superhydrophobic micro/nanostructured metal surfaces were prepared by a facile one-step electrodeposition process, including non-noble and noble metals such as copper, nickel, cadmium, zinc, gold, and palladium with (e.g. Cu) or without (e.g. Au) surface oxide films. We demonstrated by SEM and XPS that both hierarchical micro/nanostructures and spontaneous adsorption of airborne hydrocarbons endowed these surfaces with excellent superhydrophobicity. We revealed by XPS that the adsorption of airborne hydrocarbons at the Ar{sup +}-etched clean Au surface was rather quick, such that organic contamination can hardly be prevented in practical operation of surface wetting investigation. We also confirmed by XPS that ultraviolet-O{sub 3} treatment of the superhydrophobic metal surfaces did not remove the adsorbed hydrocarbons completely, but mainly oxidized them into hydrophilic oxygen-containing organic substances. We hope our findings here shed new light on deeper understanding of superhydrophobicity for micro/nanostructured metal surfaces with and without surface oxide films.

  19. Preparation

    Directory of Open Access Journals (Sweden)

    M.M. Dardir

    2014-03-01

    Full Text Available Some hexanamide-mono and di-linoleniate esters were prepared by the reaction of linolenic acid and hexanamide (derived from the reaction of hexanoic acid and diethanolamine. The chemical structure for the newly prepared hexanamide-mono and di-linoleniate esters were elucidated using elemental analysis, (FTIR, H 1NMR and chemical ionization mass spectra (CI/Ms spectroscopic techniques. The results of the spectroscopic analysis indicated that they were prepared through the right method and they have high purity. The new prepared esters have high biodegradability and lower toxicity (environmentally friendly so they were evaluated as a synthetic-based mud (ester-based mud for oil-well drilling fluids. The evaluation included study of the rheological properties, filtration and thermal properties of the ester based-muds formulated with the newly prepared esters compared to the reference commercial synthetic-based mud.

  20. Surface modification of inorganic layer compound with organic compound and preparation of thin films

    Science.gov (United States)

    Tagaya, Hideyuki; Morioka, Hiroyuki; Ogata, Sumikazu; Karasu, Masa; Kadokawa, Jun-ichi; Chiba, Koji

    1997-11-01

    Water treated Zn/Al layered double hydroxide (LDH) was prepared by the reaction of LDH oxide and water. By the reaction of the water treated Zn/Al LDH or amorphous metal hydroxide and organic oxychloride, surface modified inorganic layer compounds were prepared. Their layer structures were similar to those of the orginal LDHs except the reaction product of amorphous metal hydroxide and benzoyl chloride. Interlayer spacings of the reaction products were 0.77 to 2.67 nm depending on the size and number of function groups of organic compounds.

  1. Study of PtPd Bimetallic Nanoparticles for Fuel Cell Applications

    OpenAIRE

    Esparza, Rodrigo; Santoveña,Alan; Ruíz-Baltazar, Alvaro; Angeles-Pascual,Alvaro; Bahena,Daniel; Maya-Cornejo,Jose; Ledesma-García, Janet; Pérez,Ramiro

    2017-01-01

    Bimetallic nanoparticles are of special interest for their potential applications for fuel cells, mainly for portable power applications. Among the bimetallic systems, Pt-Pd bimetallic nanoparticles have received great interest as they can be widely used as effective catalysts for various electrochemical reactions. In this work, Pt-Pd alloy bimetallic nanoparticles were synthesized through a chemical reduction method. The nanoparticles were characterized using aberration-corrected scanning/tr...

  2. Solid phase metallurgy strategy to sub-5 nm Au-Pd and Ni-Pd bimetallic nanoparticles with controlled redox properties.

    Science.gov (United States)

    Tang, Yu; Xu, Shaodan; Dai, Yihu; Yan, Xiaoqing; Li, Renhong; Xiao, Liping; Fan, Jie

    2014-01-07

    A solid phase metallurgy strategy is applied to synthesize Au-Pd and Ni-Pd bimetallic nanoparticles (BMNPs) with a tight sub-5 nm particle size distribution. The near-surface elemental composition and redox properties of Au-Pd BMNPs can be well tailored, which leads to an optimized catalytic performance in n-hexane combustion.

  3. Bimetallic PtxCoy nanoparticles with curved faces for highly efficient hydrogenation of cinnamaldehyde

    Science.gov (United States)

    Gu, Yan; Zhao, Yonghui; Wu, Panpan; Yang, Bo; Yang, Nating; Zhu, Yan

    2016-05-01

    The control of the curved structure of bimetallic nanocrystals is a challenge, due to the rate differential for atom deposition and surface diffusion of alien atomic species on specific crystallographic planes of seeds. Herein, we report how to tune the degree of concavity of bimetallic PtxCoy concave nanoparticles using carboxylic acids as surfactants with an oleylamine system, leading to the specific crystallographic planes being exposed. The terminal carboxylic acids with a bridge ring or a benzene ring serving as structure regulators could direct the formation of curved faces with exposed high-index facets, and long-chain saturated fatty acids favored the production of curved faces with exposed low-index facets, while long-chain olefin acids alone benefited the formation of a flat surface with exposed low-index planes. Furthermore, these PtxCoy particles with curved faces displayed superior catalytic behaviour to cinnamaldehyde hydrogenation when compared with PtxCoy with flat faces. PtxCoy nanoparticles with curved faces exhibited over 6-fold increase in catalytic activity compared to PtxNiy nanoparticles with curved faces, and near 40-fold activity increase was observed in comparison with PtxFey nanoparticles with curved faces.The control of the curved structure of bimetallic nanocrystals is a challenge, due to the rate differential for atom deposition and surface diffusion of alien atomic species on specific crystallographic planes of seeds. Herein, we report how to tune the degree of concavity of bimetallic PtxCoy concave nanoparticles using carboxylic acids as surfactants with an oleylamine system, leading to the specific crystallographic planes being exposed. The terminal carboxylic acids with a bridge ring or a benzene ring serving as structure regulators could direct the formation of curved faces with exposed high-index facets, and long-chain saturated fatty acids favored the production of curved faces with exposed low-index facets, while long

  4. Rapid dechlorination of chlorinated organic compounds by nickel/iron bimetallic system in water

    Institute of Scientific and Technical Information of China (English)

    TONG Shao-ping; WEI Hong; MA Chun-an; LIU Wei-ping

    2005-01-01

    Detoxification of chlorinated organic compounds via reaction with nickel/iron powder was implemented in aqueous solution. Compared to iron, nickel/iron bimetallic powder had higher hydrodechlorination activities for both atrazine (ATR) and p-chlorophenol (pCP); nickel/iron (2.96%, w/w) was shown to have the largest specific surface area and the optimum proportion for the dechlorination of both ATR and pCP. Electrochemical measurements showed that the adsorbed hydrogen atom on the nickel must have been the dominant reductive agent for the dechlorination of both ATR andpCP in this system.

  5. Free-Standing Bimetallic Nanorings and Nanoring Arrays Made by On-Wire Lithography

    Energy Technology Data Exchange (ETDEWEB)

    Liusman, C.; Li, S. Z.; Chen, X. D.; Wei, W.; Zhang, H.; Schatz, George C.; Boey, F.; Mirkin, Chad

    2010-12-28

    This paper describes a new strategy for synthesizing free-standing bimetallic nanorings and nanoring arrays based upon on-wire lithography and a galvanic replacement reaction. The strategy allows one to tune the diameter, length, and therefore aspect ratio of the nanorings. In addition, it can be used to produce arrays of nanorings in high yield with control over number and spacing. Spectroscopic studies and discrete dipole approximation calculations show that nanoring dimers exhibit greater surface enhanced Raman scattering than the analogous nanodisk dimers.

  6. Electrical performances of pyroelectric bimetallic strip heat engines describing a Stirling cycle

    Science.gov (United States)

    Arnaud, A.; Boughaleb, J.; Monfray, S.; Boeuf, F.; Cugat, O.; Skotnicki, T.

    2015-12-01

    This paper deals with the analytical modeling of pyroelectric bimetallic strip heat engines. These devices are designed to exploit the snap-through of a thermo-mechanically bistable membrane to transform a part of the heat flowing through the membrane into mechanical energy and to convert it into electric energy by means of a piezoelectric layer deposited on the surface of the bistable membrane. In this paper, we describe the properties of these heat engines in the case when they complete a Stirling cycle, and we evaluate the performances (available energy, Carnot efficiency...) of these harvesters at the macro- and micro-scale.

  7. STUDY ON POLYMER- Ru- Co BIMETALLIC COMPLEXES CATALYSTS Ⅱ. X-RAY PHOTOELECTRON SPECTROSCOPIC ANALYSIS

    Institute of Scientific and Technical Information of China (English)

    ZONG Huijuan; TANG Qi; CHEN Zonghan; JIANG Yingyan

    1991-01-01

    Polymer-Ru-Co bimetallic complexes have been examined by X-ray photoelectron spectroscopy.The catalyst is highly active only when the mole ratio of Co/Ru is 4:3. The activity of catalysts does not depend on the total Co/Ru ratio, but on the surface stoichiometry of Co and Ru. When the relative intensities of Co2p and Ru3d of XP S peaks are close to each other and both are high, the catalyst exhibits its maximum activity.The mechanism of catalytic hydroformylation has been discussed.

  8. In vitro study of microleakage of different techniques of surface preparation used in pits and fissures

    Directory of Open Access Journals (Sweden)

    Shahrzad Javadi Nejad

    2012-01-01

    Full Text Available Objective : The purpose of this in vitro study was to evaluate the effect of different techniques of surface preparation on the microleakage of a sealant applied with traditional acid etching and self-etched bonding agent. Study Design : A total of 60 extracted third molars were randomly assigned into six groups (n = 10/each. The occlusal surfaces were sealed with a sealant (Clinpro after one of the following pretreatments: (1 phosphoric acid etching; (2 Prompt L-Pop; (3 laser + etching; (4 laser + Prompt L-Pop; (5 air abrasion + etching; (6 air abrasion + Prompt L-Pop. The specimens were immersed in a 0.5% basic fuchsin solution. Buccolingual cuts parallel to the long axis of the tooth were made. The surfaces were scored 0--2 for extent of microleakage using a microscope and the data were analyzed statistically. Results : The poorest results were obtained with laser + Prompt L-Pop which showed a greater number of specimens with microleakage (80%. Air abrasion surface preparation + phosphoric acid etching showed less microleakage than the other groups (40%. Kruskal--Wallis and t-tests revealed no significant difference in microleakage between six groups. Conclusion : The self-etching adhesive studied seems an attractive alternative to the acid-etch technique for sealant application in young children where simplifications in the clinical procedure are warranted. No significant difference was noted between the different types of enamel preparation before fissure sealant.

  9. Laser surface preparation for adhesive improvement of Ti6Al4V

    Science.gov (United States)

    Loumena, C.; Cherif, M.; Taleb Ali, M.; Jumel, J.; Kling, R.

    2017-02-01

    Titanium alloys are generally noticed for their high specific strength and their good corrosion resistance. They are widely used in light-weight structures especially in the aerospace industry. Surface preparation of Ti6Al4V for bonding improvement is conventionally performed by chemical, electrochemical pre-treatments (chromic acid anodizing, phosphate-fluoride, sol-gel,…) and/or sandblasting in order to modify the morphology and the chemistry of the surface. However, these processes produce a large volume of hazardous chemical or abrasive waste. They require high technical efforts and are therefore economically and environmentally inefficient. Laser processes could lead to a good alternative solution in terms of eco-compatibility, repeatability and ease of manufacturing. In this paper, we report on the latest developments of the collaboration between ALPhANOV and I2M institute on the laser surface preparation for adhesive bonding improvement of Ti6Al4V. We focus our investigations on the effect of pulsed laser irradiation (fluence, scan speed and lateral overlap) with a visible (515 nm) nanosecond "rod-type fibre" laser on the surface morphology and its bonding behaviour (cohesive or adhesive failure). The penetration of the adhesive in the roughness induced by laser irradiation was characterized. For this study, the surfaces were inspected by different means as optical microscopy, 3D profilometer and scanning electron microscopy (SEM). The adhesion performance of the laser treated surface was evaluated by means of DCB tests.

  10. Laser Ablation Surface Preparation of Ti-6A1-4V for Adhesive Bonding

    Science.gov (United States)

    Palmieri, Frank L.; Watson, Kent A.; Morales, Guillermo; Williams, Thomas; Hicks, Robert; Wohl, Christopher J.; Hopkins, John W.; Connell, John W.

    2012-01-01

    Adhesive bonding offers many advantages over mechanical fastening, but requires certification before it can be incorporated in primary structures for commercial aviation without disbond-arrestment features or redundant load paths. Surface preparation is widely recognized as the key step to producing robust and predictable bonds. Laser ablation imparts both topographical and chemical changes to a surface which can lead to increased bond durability. A laser based process provides an alternative to chemical-dip, manual abrasion and grit blast treatments which are expensive, hazardous, polluting, and less precise. This report documents preliminary testing of a surface preparation technique using laser ablation as a replacement for the chemical etch and abrasive processes currently applied to Ti-6Al-4V alloy adherends. Failure mode, surface roughness, and chemical makeup were analyzed using fluorescence enhanced visualization, microscopy, and X-ray photoelectron spectroscopy, respectively. Single lap shear tests were conducted on bonded and aged specimens to observe bond strength retention and failure mode. Some promising results showed increasing strength and durability of lap shear specimens as laser ablation coverage area and beam intensity increased. Chemical analyses showed trends for surface chemical species which correlated with improved bond strength and durability. Combined, these results suggest that laser ablation is a viable process for inclusion with or/and replacement of one or more currently used titanium surface treatments. On-going work will focus on additional mechanical tests to further demonstrate improved bond durability.

  11. A bimetallic nanocomposite electrode for direct and rapid biosensing of p53 DNA plasmid

    Indian Academy of Sciences (India)

    Ezat Hamidi-Asl; Jahan-Bakhsh Raoof; Nahid Naghizadeh; Simin Sharifi; Mohammad Saeid Hejazi

    2015-09-01

    A new label-free electrochemical DNA biosensor is presented based on carbon paste electrode (CPE) modified with gold (Au) and platinum (Pt) nanoparticles to prepare the bimetallic nanocomposite electrode. The proposed sensor was made by immobilization of 15-mer single stranded oligonucleotide probe related to p53 gene for detection of DNA plasmid samples. The hybridization detection relied on the alternation in the guanine oxidation signal following hybridization of the probe with complementary genomic DNA.The technique of differential pulse voltammetry (DPV) was used for monitoring guanine oxidation. To optimize the performance of the modified CPE, different electrodes were prepared in various percentages of Au and Pt nanoparticles. The modified electrode containing 15% Au/Pt bimetallic nanoparticles (15% Au/Pt-MCPE) was selected as the best working electrode. The selectivity of the sensor was investigated using plasmid samples containing non-complementary oligonucleotides. The detection limit of the biosensor was studied and calculated to be 53.10 pg L−1.

  12. Reactive carbon microspheres prepared by surface-grafting 4-(chloromethyl)phenyltrimethoxysilane for preparing molecularly imprinted polymer

    Science.gov (United States)

    Liu, Weifeng; Zhao, Huijun; Yang, Yongzhen; Liu, Xuguang; Xu, Bingshe

    2013-07-01

    Carbon microspheres (CMSs) were oxidized by a mixture of concentrated sulfuric and nitric acids, and modified by 4-(chloromethyl)phenyltrimethoxysilane to give reactive surface. Then, by adopting the surface molecular imprinting technique, dibenzothiophene (DBT) molecule-imprinted material MIP-DBT/CMSs was prepared with methacrylic acid as functional monomer and ethylene glycol dimethacrylate as crosslinking agent. The binding character of MIP-DBT/CMSs toward DBT was investigated with static method by gas chromatography, using fluorene and biphenyl as the reference substances which are similar to DBT in chemical structure to a certain extent. The effects of reaction time, temperature, and coupling agent concentration during silanization were investigated. The results show that the optimized conditions of silanization were 0.3 g oxidized-CMSs, 5% of CMTMS, 80 °C and 4 h. On the basis of silanized-CMSs, MIP-DBT/CMSs was synthesized. The adsorption results show that MIP-DBT/CMSs possessed strong adsorption ability for DBT. The maximal adsorption amount reached up 88.83 mg/g, in comparison with 44.51 mg/g of the non-imprinted polymer. In addition, MIP-DBT/CMSs exhibited a good selective adsorption capacity for DBT than fluorene (19.86 mg/g) and biphenyl (15.33 mg/g). The adsorption behavior followed the pseudo second order kinetic model. And the Freundlich isotherm was found to describe well the equilibrium adsorption data.

  13. TECHNOLOGICAL ADVANCEMENT OF DEPOSIT WELDING AND GAS LASER CUTTING TO INCREASE THE EFFICIENCY OF THE BIMETALLIC TOOL PRODUCTION

    Directory of Open Access Journals (Sweden)

    Burlachenko Oleg Vasil’evich

    2017-08-01

    Full Text Available Deposit welding is the application of a layer of metal on the surface of a product using fusion welding. In this paper, we consider the method of improving the technology of gas laser cutting, which makes it possible to achieve a high productivity of manufacturing a bimetallic tool. The present paper is concerned with the advantages of gas laser cutting which allows to consider this particular process of separating materials as highly-productive, low-waste, and advanced method of removing allowances of weld-deposit high-speed steel on the working surfaces of bimetallic tool. Urgency of the use of deposit welding and gas laser cutting to improve the efficiency of production of bimetallic tool is shown. The comparative analysis of gas-laser cutting and other cutting methods is given according to the geometrical parameters of cutting and surface quality. Analysis of the results of experimental studies has confirmed the high technological attractiveness and economic efficiency of manufacturing composite structures of punches and matrices when applying deposit welding of cutting parts with high-speed steels. The cost of dimensional processing of the welded cutting part is reduced by 4 to 6 times, while the manufacturing time is reduced by 6 to 12 times.

  14. Comparison of linear dimensional change, surface hardness and surface roughness of refractory model prepared from two different duplicating media.

    Science.gov (United States)

    Porwal, Amit; Chandrashekhar, Naveen H; Nadiger, Ramesh K; Meshramkar, Roseline D; Guttal, Satyabodh S

    2011-03-01

    The aim of this study was to evaluate and compare the linear dimensional change, surface hardness and surface roughness of the refractory casts poured against different duplicating media. Polyvinyl siloxane and Agar-agar were used for duplicating the stainless steel die. Sixty refractory models were prepared which were divided into two groups: I and II with 30 samples each respectively. Each group was subdivided into 3 subgroups with 10 samples each which were treated differently. All the specimens were measured for the linear dimensional change and surface hardness and the obtained data was statistically analyzed. Surface roughness was evaluated qualitatively taking SEM photomicrographs. Statistical analysis of linear dimensional change using one-way ANOVA showed statistically significant difference between subgroups of group I and non-significant difference between subgroups of group II. One-way ANOVA for Brinell hardness number showed statistically significant difference between the subgroups of group I & II. Student's 't' test results for linear dimensional change among different subgroups of group I & II showed significant difference between IA-IIA, IB-IIB, IC-IIC. Similarly 't'-test results for Brinell hardness number showed significant difference between subgroups IA-IIA, IB-IIB, and IC-IIC. Surface characteristics of the refractory casts poured against polyvinyl siloxane duplicating media were found to be better than the Agar media.

  15. Designing and preparation of cytisine alkaloid surface-imprinted material and its molecular recognition characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Baojiao, E-mail: gaobaojiao@126.com [Department of Chemical Engineering, North University of China, Taiyuan 030051 (China); Bi, Concon [Department of Chemical Engineering, North University of China, Taiyuan 030051 (China); Fan, Li [School of Chemistry and Chemical Engineering, Shanxi University, Taiyuan 030006 (China)

    2015-03-30

    Highlights: • An elaborate molecular design was well done for molecule surface-imprinting. • The new method of “pre-graft polymerizing and post-imprinting” was used. • Cytisine molecule surface-imprinted material was prepared. • Cytisine surface-imprinting depends on electrostatic interaction between host–guest. • The imprinted material has special recognition selectivity for template cytisine. - Abstract: Based on molecular design, a cytisine surface-imprinted material was prepared using the new surface-imprinting technique of “pre-graft polymerizing and post-imprinting”. The graft-polymerization of glycidyl methacrylate (GMA) on the surfaces of micron-sized silica gel particles was first performed with a surface-initiating system, preparing the grafted particles PGMA/SiO{sub 2}. Subsequently, a polymer reaction, the ring-opening reaction of the epoxy groups of the grafted PGMA, was conducted with sodium 2,4-diaminobenzene sulfonate (SAS) as reagent, resulting in the functional grafted particles SAS-PGMA/SiO{sub 2}. The adsorption of cytisine on SAS-PGMA/SiO{sub 2} particles reached saturation via strong electrostatic interaction between the sulfonate groups of SAS-PGMA/SiO{sub 2} particles and the protonated N atoms in cytisine molecule. Finally, cytisine surface-imprinting was successfully carried out with glutaraldehyde as crosslinker, obtaining cytisine surface-imprinted material MIP-SASP/SiO{sub 2}. The binding and recognition characteristics of MIP-SASP/SiO{sub 2} towards cytisine were investigated in depth. The experimental results show that there is strong electrostatic interaction between particles and cytisine molecules, and on this basis, cytisine surface-imprinting can be smoothly performed. The surface-imprinted MIP-SASP/SiO{sub 2} has special recognition selectivity and excellent binding affinity for cytisine, and the selectivity coefficients of MIP-SASP/SiO{sub 2} particles for cytisine relative to matrine and oxymatrine, which

  16. Preparation and surface modification of magnetic poly(methyl methacrylate) microspheres

    Institute of Scientific and Technical Information of China (English)

    YANG Chengli; GUAN Yueping; XING Jianmin; LIU Junguo; AN Zhentao; LIU Huizhou

    2004-01-01

    A novel method for preparation of magnetic polymer microspheres by spraying suspension polymerization (SSP) was developed. Relatively uniform magnetic poly(methyl methacrylate) microspheres were prepared by the spraying suspension polymerization (SSP)using methyl methacrylate (MMA) as monomer, divinylbenzene (DVB) as cross-linking agent,benzoyl peroxide (BPO) as initiator and polyvinyl alcohol (PVA) as stabilizer in the presence of hydrophobic Fe3O4 magnetic fluid. The microspheres prepared were modified by surface chemical reaction. The magnetic properties and morphology of the microspheres were examined by SEM and VSM respectively. The active functional groups of microspheres were examined by infrared spectra. The results showed that microspheres with saturation magnetization of 16.8emu/g showed distinct superparamagnetic characteristics and the magnetic microspheres with a size of 10 μm were relatively uniform.

  17. Silver nanoplates: controlled preparation, self-assembly, and applications in surface-enhanced Raman scattering

    Science.gov (United States)

    Yi, Zao; Xu, Xibin; Wu, Xiaoqiang; Chen, Chaohua; Li, Xibo; Luo, Bingchi; Luo, Jiangshan; Jiang, Xiaodong; Wu, Weidong; Yi, Yougen; Tang, Yongjian

    2013-02-01

    Silver nanoplates were prepared in a dual reduction system with NaBH4 and sodium citrate both as reducing agents. And then the as-prepared nanoplates could be growing up through multistage growth methodology. The average edge length of Ag nanoplates can be tailored from 40 nm to 260 nm without changing their shape, crystallinity, and the average thickness. Furthermore, the effectiveness of these silver nanoplates as substrates prepared by the silanization self-assembly method toward surface-enhanced Raman scattering (SERS) detection was evaluated by using 4-aminothiophenol (4-ATP) and rhodamine 6G (R6G) as probe molecules. It was found that the enhancement ability of the silver nanoplates film is remarkable lower than that of the spherical silver nanoparticle film. The reason is attributed to the electromagnetic mechanism and chemical mechanism. This work will be of great significance in understanding the SERS enhancement mechanism and in the fabrication of nanoparticle films for biosensing.

  18. Bonding durability between acrylic resin adhesives and titanium with surface preparations.

    Science.gov (United States)

    Yanagida, Hiroaki; Minesaki, Yoshito; Matsumura, Kousuke; Tanoue, Naomi; Muraguchi, Koichi; Minami, Hiroyuki

    2017-01-31

    The purpose of the present study was to evaluate the efficacy of pretreatment on the bonding durability between titanium casting and two acrylic adhesives. Cast titanium disk specimens treated with four polymer-metal bonding systems as follow: 1) air-abraded with 50-70 μm alumina, 2) 1)+Alloy Primer, 3) 1)+M.L. Primer and 4) tribochemical silica/silane coating system (Rocatec System). The specimens were bonded with M bond or Super-bond C&B adhesive. The shear bond strengths were determined before and after thermocycling (20,000 cycles). The surface characteristics after polishing, and for the 1) and 4) preparations were determined. The bond strengths for all combinations significantly decreased after thermocycling. The combination of Super-bond C&B adhesive and 2) led to significantly higher bond strength than the other preparations after thermocycling. The maximum height of the profile parameters for the polishing group was lower than other preparations.

  19. Reforming of oxygenates for H2 production: correlating reactivity of ethylene glycol and ethanol on Pt(111) and Ni/Pt(111) with surface d-band center.

    Science.gov (United States)

    Skoplyak, Orest; Barteau, Mark A; Chen, Jingguang G

    2006-02-02

    The dehydrogenation and decarbonylation of ethylene glycol and ethanol were studied using temperature programmed desorption (TPD) on Pt(111) and Ni/Pt(111) bimetallic surfaces, as probe reactions for the reforming of oxygenates for the production of H2 for fuel cells. Ethylene glycol reacted via dehydrogenation to form CO and H2, corresponding to the desired reforming reaction, and via total decomposition to produce C(ad), O(ad), and H2. Ethanol reacted by three reaction pathways, dehydrogenation, decarbonylation, and total decomposition, producing CO, H2, CH4, C(ad), and O(ad). Surfaces prepared by deposition of a monolayer of Ni on Pt(111) at 300 K, designated Ni-Pt-Pt(111), displayed increased reforming activity compared to Pt(111), subsurface monolayer Pt-Ni-Pt(111), and thick Ni/Pt(111). Reforming activity was correlated with the d-band center of the surfaces and displayed a linear trend for both ethylene glycol and ethanol, with activity increasing as the surface d-band center moved closer to the Fermi level. This trend was opposite to that previously observed for hydrogenation reactions, where increased activity occurred on subsurface monolayers as the d-band center shifted away from the Fermi level. Extrapolation of the correlation between activity and the surface d-band center of bimetallic systems may provide useful predictions for the selection and rational design of bimetallic catalysts for the reforming of oxygenates.

  20. Surface Structure Spread Single Crystals ((SC)-C-4): Preparation and characterization

    Energy Technology Data Exchange (ETDEWEB)

    de Alwis, A; Holsclaw, B; Pushkarev, V V; Reinicker, A; Lawton, T J; Blecher, M E; Sykes, E C. H.; Gellman, A J

    2013-02-01

    A set of six spherically curved Cu single crystals referred to as Surface Structure Spread Single Crystals (S{sup 4}Cs) has been prepared in such a way that their exposed surfaces collectively span all possible crystallographic surface orientations that can be cleaved from the face centered cubic Cu lattice. The method for preparing these S{sup 4}Cs and for finding the high symmetry pole point are described. Optical profilometry has been used to determine the true shapes of the S{sup 4}Cs and show that over the majority of the surface, the shape is extremely close to that of a perfect sphere. The local orientations of the surfaces lie within ±1{degree} of the orientation expected on the basis of the spherical shape; their orientation is as good as that of many commercially prepared single crystals. STM imaging has been used to characterize the atomic level structure of the Cu(111)±11{degree}-S{sup 4}C. This has shown that the average step densities and the average step orientations match those expected based on the spherical shape. In other words, although there is some distribution of step-step spacing and step orientations, there is no evidence of large scale reconstruction or faceting. The Cu S{sup 4}Cs have local structures based on the ideal termination of the face centered cubic Cu lattice in the direction of termination. The set of Cu S{sup 4}Cs will serve as the basis for high throughput investigations of structure sensitive surface chemistry on Cu.

  1. Effect of preparation surface area on the clinical outcome of full veneer crowns in dogs.

    Science.gov (United States)

    Riehl, Jessica; Soukup, Jason W; Collins, Caitlyn; Siverling, Sarah; Ploeg, Heidi-Lynn; Snyder, Christopher J

    2014-01-01

    Crown therapy is commonly used in veterinary medicine to provide support to teeth which have previously fractured, received root canal therapy, have significant wear, or experienced other detrimental removal of tooth substance. As with several aspects of veterinary medicine, many of the recommendations or guidelines for crown therapy originate from human dentistry, which are then transferred to veterinary patients. Due to the significant difference in the anatomy of teeth and function of the oral cavity between humans and dogs, these guidelines need to be studied to determine the appropriateness of their use in veterinary patients. This article evaluates the relationship between surface area of the preparation and clinical outcome of full veneer crown therapy of the canine tooth in dogs. Although there appeared to be a positive relationship between preparations with greater surface area and successful clinical outcome, it was not found to be statistically significant.

  2. Recognizing Amino Acid Chirality with Surface-Imprinted Polymers Prepared in W/O Emulsions

    Directory of Open Access Journals (Sweden)

    Min Jae Shin

    2013-01-01

    Full Text Available A molecularly imprinted polymer was prepared by a surface molecular imprinting technique in water-in-oil (W/O emulsion. In this technique, the solid polymer, which is molecularly imprinted at the internal cavity surface, is prepared by polymerizing W/O emulsions consisting of a water-soluble imprinted molecule, a functional host molecule, an emulsion stabilizer, and a crosslinking agent. Dioleoyl phosphate was used as an emulsion stabilizer, and this compound also acted as a monomer and a host functional group in the imprinted cavity. Divinylbenzene was used as a crosslinker. Tryptophan methyl ester and phenylalanine methyl ester were used as the target template materials. These imprinted polymers exhibited enantiomeric selectivity in absorption experiments, and the maximum separation factor was 1.58. The enantiomeric selectivity with tryptophan methyl ester was higher than that with phenylalanine methyl ester.

  3. Gold Nanostructures for Surface-Enhanced Raman Spectroscopy, Prepared by Electrodeposition in Porous Silicon

    Directory of Open Access Journals (Sweden)

    Yukio H. Ogata

    2011-04-01

    Full Text Available Electrodeposition of gold into porous silicon was investigated. In the present study, porous silicon with ~100 nm in pore diameter, so-called medium-sized pores, was used as template electrode for gold electrodeposition. The growth behavior of gold deposits was studied by scanning electron microscope observation of the gold deposited porous silicon. Gold nanorod arrays with different rod lengths were prepared, and their surface-enhanced Raman scattering properties were investigated. We found that the absorption peak due to the surface plasmon resonance can be tuned by changing the length of the nanorods. The optimum length of the gold nanorods was ~600 nm for surface-enhanced Raman spectroscopy using a He-Ne laser. The reason why the optimum length of the gold nanorods was 600 nm was discussed by considering the relationship between the absorption peak of surface plasmon resonance and the wavelength of the incident laser for Raman scattering.

  4. Bioactive titanium metal surfaces with antimicrobial properties prepared by anodic oxidation treatment

    Institute of Scientific and Technical Information of China (English)

    YUE ChongXia; YANG BangCheng; ZHANG XingDong

    2009-01-01

    In order to endow titanium metals with bioactivity and antimicrobial properties,titanium plates were subjected to anodic oxidation treatment in NaCI solutions in this study.The treated titanium metals could induce apatite formation in the fast calcification solution,and osteoblasts on the treated titanium surfaces proliferated well as those on the untreated titanium metal surfaces.The treated metals could inhibit S.aureus growth in the microbial culture experiments.It was assumed that Ti-OH groups and Ti-CI groups formed on the treated titanium surface were responsible for the bioactivity and antimicrobial properties of the metals.The anodic oxidation treatment was an effective way to prepare bioactive titanium surfaces with antimicrobial properties.

  5. Preparation of porous microstructures on NiTi alloy surface with femtosecond laser pulses

    Institute of Scientific and Technical Information of China (English)

    LIANG ChunYong; YANG Yang; WANG HongShui; YANG JianJun; YANG XianJin

    2008-01-01

    Porous microstructures on Nickel-Titanium (NiTi) alloy surfaces were prepared by linearly polarized femtosecond lasers with moving focal point at a certain speed. It was found that various novel micro-structures from feather-like ripples to cluster-like porous textures could be formed with increasing laser energy. Particularly, when the laser energy was 400 μJ, a periodic porous metal surface was gen-erated. Measurement of X-ray diffraction showed that the grains on the sample surface were refined through femtosecond laser ablation processes, but the crystal structures still kept their original states. Analysis by X-ray photoelectron spectroscopy revealed that Ni/Ti on the sample surface was changed with an evident oxidization of titanium element under different laser energies. This investigation pro-vides a new approach to improve the biocompatibility of NiTi-based implant devices.

  6. Preparation of silver material used for detection of biocomplexes by surface-enhanced Raman scattering

    Science.gov (United States)

    Nowak, M.; Binczyk, M.; Skrobanska, M.; Marciniak, L.; Runka, T.; Jastrzab, R.

    2016-08-01

    Silver dendrites were obtained on Cu plate by a classic galvanic displacement process. The process of preparing Ag particles was performed at different immersion times in AgNO3 solution, and the best process parameters were selected according to the enhancement effect of the Raman spectra of Rhodamine 6G. Ag-Cu substrates were chosen for a Surface-enhanced Raman scattering (SERS) study of biocomplexes because their preparation is cost effective and simple, and the relative homogeneous signal enhancement on the prepared silver SERS-active substrate was obtained. The rapid process of surface preparation was applied to identify the mode of coordination. Biocomplexes of Co and Ni ions with adenosine triphosphate form in neutral pH were immersed on the Ag dendrites, and SERS spectra of these compounds were collected. This research work was carried out in order to determine different types of coordination in the same pH conditions and relatively low concentration using SERS which is an emerging and promising technique for the determination of coordination types in biocomplexes.

  7. A Surface Damage Investigation on Uniaxial Tensile Test Specimens Prepared by Common Cutting Methods

    Science.gov (United States)

    1981-02-01

    REPORI’ A SURFACE DAMAGE INVESTIGATION ON UNIAXIAL TENSILE TEST SPECIMENSPREPARED BY COMMON CUTTING METHODS JUN 2 1931 THOMAS J. C. CHEW DALE A...Sýrfa-i-mage Investigation on Uniaxial Tensile Test Specimens Prepared by Common Cutting Method I Spi-.i t’ ,, ., • T7. AUTHORý#) . _" ’ /t’ .• r...Saw 10 2.1.3 Cutting by Milling Machine 11 2.1.4 Cutting by Die Cutter 11 2.2 Uniaxial Tensile Test 12 2.3 Electron Microscope Surface Examination 13 3

  8. Obliquely Deposited Gold Nanohelices on Lithography-Free Prepared Nanoseeded Surfaces

    Science.gov (United States)

    Jen, Yi-Jun; Liu, Wei-Chih; Hsiao, Chih-Yung; Lin, Po-Cheng; Yu, Chia-Liang; Chan, Teh-Li

    2017-08-01

    A substrate surface on which gold particles are distributed is prepared by annealing an ultra-thin gold film to enable glancing angle deposition. By cooling the substrate and controlling its spin rate, two spiral-like and one screw-like gold nanohelix arrays are grown upon the seeded surfaces. The mean helix radius and pitch length are reduced to 17 and 55 nm, respectively. The g-factor of the three nanohelix arrays is measured here and associated circular dichroism peak blue shifts occur as the gold helices shrink.

  9. Preparation and UV-light Absorption Property of Oleic Acid Surface Modified ZnO Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    KANG Jong-hun; GUO Yu-peng; CHEN Yue; WANG Zi-chen

    2011-01-01

    Syntheses of zince oxide(ZnO) nanoparticles by direct precipitation and surface modification with oleic acid were reported. ZnO nanoparticles were characterized via X-ray diffractometry(XRD), transmission electron microscopy(TEM), infrared spectroscopy(IR) and UV-Vis spectroscopy. The prepared ZnO nanoparticles were nearly spherical and highly crystalline with an average size of 29 nm. In addition, high UV-light absorption properties of oleic acid surface modified ZnO nanoparticles were successfully obtained for a dispersion of ZnO nanoparticles in ethanol.

  10. Preparation and characterization of superhydrophobic surfaces based on hexamethyldisilazane-modified nanoporous alumina

    Directory of Open Access Journals (Sweden)

    Sanli Deniz

    2011-01-01

    Full Text Available Abstract Superhydrophobic nanoporous anodic aluminum oxide (alumina surfaces were prepared using treatment with vapor-phase hexamethyldisilazane (HMDS. Nanoporous alumina substrates were first made using a two-step anodization process. Subsequently, a repeated modification procedure was employed for efficient incorporation of the terminal methyl groups of HMDS to the alumina surface. Morphology of the surfaces was characterized by scanning electron microscopy, showing hexagonally ordered circular nanopores with approximately 250 nm in diameter and 300 nm of interpore distances. Fourier transform infrared spectroscopy-attenuated total reflectance analysis showed the presence of chemically bound methyl groups on the HMDS-modified nanoporous alumina surfaces. Wetting properties of these surfaces were characterized by measurements of the water contact angle which was found to reach 153.2 ± 2°. The contact angle values on HMDS-modified nanoporous alumina surfaces were found to be significantly larger than the average water contact angle of 82.9 ± 3° on smooth thin film alumina surfaces that underwent the same HMDS modification steps. The difference between the two cases was explained by the Cassie-Baxter theory of rough surface wetting.

  11. Preparation and characterization of reconstructed small intestinal brush border membranes for surface plasmon resonance analysis.

    Science.gov (United States)

    Cho, Sungpil; Park, Jae Hyung; Yu, Jaehoon; Lee, Yong-Kyu; Byun, Youngro; Chung, Hesson; Kwon, Ick Chan; Jeong, Seo Young

    2004-01-01

    To prepare the surface generated by small intestinal brush border membrane vesicles (BBMVs) for the surface plasmon resonance (SPR) analysis, which allows the real-time measurement of binding events occurring on the intestinal membrane. BBMVs were isolated from Sprague-Dawley rats, suspended in HEPES-buffered saline, and flowed over the surface of a SPR sensor chip composed of dextran derivatives modified with lipophilic residues. The surface coverage was determined from binding of bovine serum albumin to BBMV-immobilized sensor chip. The performance of BBMVs immobilized was evaluated by their interaction with otilonium bromide and bile salts. The stable BBMV surface was achieved when BBMV suspension was flowed over the sensor chip for 8 h at a rate of 2 microl/min. The flow of otilonium bromide resulted in an increased SPR signal because of its binding to calcium channel, which is known to be distributed over the gastrointestinal tact. When bile salts were flowed over ileal and duodenal BBMV surfaces, respectively, a slightly higher SPR signal was observed in the ileal BBMV surface, indicating the specific interaction of bile salts with bile acid transporters. BBMV surfaces may be useful for the estimation of binding events on the intestinal membrane by SPR analysis, especially for the drugs that are orally administrated.

  12. A facile method for preparing highly conductive and reflective surface-silvered polyimide films

    Science.gov (United States)

    Liao, Yuan; Cao, Bing; Wang, Wen-Cai; Zhang, Liqun; Wu, Dezhen; Jin, Riguang

    2009-07-01

    A novel method was developed for the preparation of reflective and electrically conductive surface-silvered polyimide (PI) films. The polyimide films were functionalized with poly(dopamine), simply by dipping the PI films into aqueous dopamine solution and mildly stirring at room temperature. Electroless plating of silver was readily carried out on the poly(dopamine) deposited PI (PI-DOPA) surface. The surface compositions of the modified PI films were studied by X-ray photoelectron spectroscopy (XPS). XPS results show that the PI-DOPA surfaces were successfully deposited with ploy(dopamine) and were ready for electroless deposition of silver. The poly(dopamine) layer was used not only as the chemi-sorption sites for silver particles during the electroless plating of silver, but also as an adhesion promotion layer for the electrolessly deposited silver. The as-prepared silvered PI films show high conductivity and reflectivity, with a surface resistance of 1.5 Ω and a reflectivity of 95%, respectively.

  13. A facile method for preparing highly conductive and reflective surface-silvered polyimide films

    Energy Technology Data Exchange (ETDEWEB)

    Liao Yuan; Cao Bing [State Key Laboratory of Chemical Resource Engineering, and the Key Laboratory of Beijing City on Preparation and Processing of Novel Polymer Materials, Beijing University of Chemical Technology, 15 Beisanhuan East Road, Beijing 100029 (China); Wang Wencai, E-mail: wangw@mail.buct.edu.cn [State Key Laboratory of Chemical Resource Engineering, and Key Laboratory of Beijing City on Preparation and Processing of Novel Polymer Materials, Beijing University of Chemical Technology, 15 Beisanhuan East Road, Beijing 100029 (China); Zhang Liqun; Wu Dezhen; Jin Riguang [State Key Laboratory of Chemical Resource Engineering, and Key Laboratory of Beijing City on Preparation and Processing of Novel Polymer Materials, Beijing University of Chemical Technology, 15 Beisanhuan East Road, Beijing 100029 (China)

    2009-07-15

    A novel method was developed for the preparation of reflective and electrically conductive surface-silvered polyimide (PI) films. The polyimide films were functionalized with poly(dopamine), simply by dipping the PI films into aqueous dopamine solution and mildly stirring at room temperature. Electroless plating of silver was readily carried out on the poly(dopamine) deposited PI (PI-DOPA) surface. The surface compositions of the modified PI films were studied by X-ray photoelectron spectroscopy (XPS). XPS results show that the PI-DOPA surfaces were successfully deposited with ploy(dopamine) and were ready for electroless deposition of silver. The poly(dopamine) layer was used not only as the chemi-sorption sites for silver particles during the electroless plating of silver, but also as an adhesion promotion layer for the electrolessly deposited silver. The as-prepared silvered PI films show high conductivity and reflectivity, with a surface resistance of 1.5 {Omega} and a reflectivity of 95%, respectively.

  14. Preparation of biomimetic hydrophobic coatings on AZ91D magnesium alloy surface

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The hydrophobic coating has been a promising technology for improving surface performance. The surface performance of magnesium alloy has been limited in application. Furthermore, the hydrophobic of magnesium alloy is rarely investigated because magnesium alloy is an active metal alloy. In this paper, inspired by microstructure character of typical plant leaf surface such as lotus, the biomimetic hydrophobic coatings on AZ91D magnesium alloy surface were prepared by means of wet-chemical combining electroless. The samples were immersed into AgNO3 solution in wet-chemical method firstly. Then, biomimetic hydrophobic coatings were prepared by electroless after wet-method pretreatment. The microstructure was observed by SEM and the contact angles were measured by contact angle tester. The results indicated that the biomimetic hydrophobic coatings with uniform crystalline and dense structure could be obtained on AZ91D magnesium alloy surface. The results of contact angle revealed that the biomimetic nano-composite coatings were hydrophobic. The wet-chemical method treatment on the AZ91D magnesium alloy substrate provided a rough microstructure, thus improving adhesion of the coating and the substrate.

  15. Preparation and Rapid Analysis of Antibacterial Silver, Copper and Zinc Doped Sol–gel Surfaces

    OpenAIRE

    Jaiswal, Swarna; Duffy, Brendan; McHale, Patrick

    2012-01-01

    The colonisation of clinical and industrial surfaces with microorganisms, including antibiotic-resistant strains, has promoted increased research into the development of effective antibacterial and antifouling coatings. This study describes the preparation of metal nitrate (Ag, Cu, Zn) doped methyltriethoxysilane (MTEOS) coatings and the rapid assessment of their antibacterial activity using polyproylene microtitre plates. Microtitre plate wells were coated with different volumes of liquid so...

  16. Polyelectrolyte complexes : Preparation, characterization, and use for control of wet and dry adhesion between surfaces

    OpenAIRE

    Ankerfors, Caroline

    2012-01-01

    This thesis examines polyelectrolyte complex (PEC) preparation, adsorption behaviour, and potential use for control of wet and dry adhesion between surfaces. PEC formation was studied using a jet-mixing method not previously used for mixing polyelectrolytes. The PECs were formed using various mixing times, and the results were compared with those for PECs formed using the conventional polyelectrolyte titration method. The results indicated that using the jet mixer allowed the size of the form...

  17. A simple and highly effective process for the preparation of activated carbons with high surface area

    Energy Technology Data Exchange (ETDEWEB)

    Li Ying, E-mail: liyingjlu@163.com [College of Chemistry, Jilin University, Changchun 130012 (China); Ding Xuefeng; Guo Yupeng; Wang Lili; Rong Chunguang; Qu Yuning; Ma Xiaoyu [College of Chemistry, Jilin University, Changchun 130012 (China); Wang Zichen, E-mail: wangzc@jlu.edu.cn [College of Chemistry, Jilin University, Changchun 130012 (China)

    2011-06-15

    Highlights: {yields} High surface area activated carbon can be prepared by rice husk H{sub 3}PO{sub 4} without pretreatment. {yields} The characteristics of the activated carbon were greatly influenced by post-processing method. {yields} The lower SiO{sub 2} content of the activated carbons, the higher pore volume the carbons had. {yields} Some silica in rice husk reacted with H{sub 3}PO{sub 4} to form SiP{sub 2}O{sub 7} which could be removed by post-process. - Abstract: Activated carbons with high surface area were prepared by phosphoric acid as activation agent and rice husks as precursors. It was found that the characteristics of the activated carbons were influenced not only by the preparation but also by the post-processing method. The high surface area of the activated carbons was prepared under the optimum condition (50% H{sub 3}PO{sub 4} with impregnation ratio of 5:1, activation temperature of 500 deg. C, activation time of 0.5 h, wash water temperature of 100 deg. C). SiO{sub 2} content could affect the surface area of activated carbons, either. The lower SiO{sub 2} content of the activated carbons, the higher pore volume the carbons had. The SiO{sub 2} content was 11.2% when used the optimum condition. The explanation was that silicon element in rice husks reacted with H{sub 3}PO{sub 4} to form silicon phosphate (SiP{sub 2}O{sub 7}), and it could be proved further by X-ray diffraction analysis, SiP{sub 2}O{sub 7} could be removed by post-process.

  18. Designing and preparation of cytisine alkaloid surface-imprinted material and its molecular recognition characteristics

    Science.gov (United States)

    Gao, Baojiao; Bi, Concon; Fan, Li

    2015-03-01

    Based on molecular design, a cytisine surface-imprinted material was prepared using the new surface-imprinting technique of "pre-graft polymerizing and post-imprinting". The graft-polymerization of glycidyl methacrylate (GMA) on the surfaces of micron-sized silica gel particles was first performed with a surface-initiating system, preparing the grafted particles PGMA/SiO2. Subsequently, a polymer reaction, the ring-opening reaction of the epoxy groups of the grafted PGMA, was conducted with sodium 2,4-diaminobenzene sulfonate (SAS) as reagent, resulting in the functional grafted particles SAS-PGMA/SiO2. The adsorption of cytisine on SAS-PGMA/SiO2 particles reached saturation via strong electrostatic interaction between the sulfonate groups of SAS-PGMA/SiO2 particles and the protonated N atoms in cytisine molecule. Finally, cytisine surface-imprinting was successfully carried out with glutaraldehyde as crosslinker, obtaining cytisine surface-imprinted material MIP-SASP/SiO2. The binding and recognition characteristics of MIP-SASP/SiO2 towards cytisine were investigated in depth. The experimental results show that there is strong electrostatic interaction between particles and cytisine molecules, and on this basis, cytisine surface-imprinting can be smoothly performed. The surface-imprinted MIP-SASP/SiO2 has special recognition selectivity and excellent binding affinity for cytisine, and the selectivity coefficients of MIP-SASP/SiO2 particles for cytisine relative to matrine and oxymatrine, which were used as two contrast alkaloids, are 9.5 and 6.5, respectively.

  19. Synthesis, characterization and antibacterial activity of copper, nickel and bimetallic Cu–Ni nanoparticles for potential use in dental materials

    Directory of Open Access Journals (Sweden)

    Liliana Argueta-Figueroa

    2014-08-01

    Full Text Available The antibacterial effect is a desirable property in dental materials. Development of simple methods for the preparation of nanosized metal particles has attracted significant attention because of their future applications due to unusual size-dependent antibacterial properties. Copper (Cu, Nickel (Ni and bimetallic Cu–Ni nanoparticles were prepared by a simple chemical method and their antibacterial activity was tested against the widely used standard human pathogens Staphylococcus aureus (gram-negative and Escherichia coli (gram-positive. Additionally, these nanoparticles were tested against the dental pathogen Streptococcus mutans. Our results are promising for potential use in dental materials science.

  20. Synthesis, characterization and antibacterial activity of copper, nickel and bimetallic Cu-Ni nanoparticles for potential use in dental materials

    Institute of Scientific and Technical Information of China (English)

    Liliana Argueta-Figueroa; Raúl A. Morales-Luckie; Rogelio J. Scougall-Vilchis; Oscar F. Olea-Mejía

    2014-01-01

    The antibacterial effect is a desirable property in dental materials. Development of simple methods for the preparation of nanosized metal particles has attracted significant attention because of their future applications due to unusual size-dependent antibacterial properties. Copper (Cu), Nickel (Ni) and bimetallic Cu-Ni nanoparticles were prepared by a simple chemical method and their antibacterial activity was tested against the widely used standard human pathogens Staphylococcus aureus (gram-negative) and Escherichia coli (gram-positive). Additionally, these nanoparticles were tested against the dental pathogen Streptococcus mutans. Our results are promising for potential use in dental materials science.

  1. Structural, electronic and adsorption properties of Rh(111)/Mo(110) bimetallic catalyst: A DFT study

    Science.gov (United States)

    Palotás, K.; Bakó, I.; Bugyi, L.

    2016-12-01

    Geometric and electronic characterizations of one monolayer rhodium with Nishiyama-Wassermann (NW) structure on Mo(110) substrate have been performed by density functional theory (DFT) calculations. In the NW structure the Rh atoms form a wavy structure propagating along the [001] direction, characterized by an amplitude of 0.26 Å in the [110] direction and by 0.10 Å in the [110] direction of the Mo(110) substrate. Strain and ligand effects operating in the rhodium film are distinguished and found to be manifested in the downward shift of the d-band center of the electron density of states (DOS) by 0.11 eV and 0.18 eV, respectively. The shift in the d-band center of Rh DOS predicts a decrease in the surface reactivity toward CO adsorption, which has been verified by detailed calculations of bond energies of CO located at on-top, bridge and hollow adsorption sites. The CO adsorption energies are decreased by about 35% compared to those reported for pure Rh(111), offering novel catalytic pathways for the molecule. An in-depth analysis of the charge transfer and the partial DOS characters upon CO adsorption on the NW-structured Rh(111)/Mo(110) bimetallic catalyst and on the pure Rh(111) surface sheds light on the bonding mechanism of CO and on the governing factors determining its lowered bond energy on the bimetallic surface.

  2. Catalytic activity of nanostructured Au: Scale effects versus bimetallic/bifunctional effects in low-temperature CO oxidation on nanoporous Au

    Directory of Open Access Journals (Sweden)

    Lu-Cun Wang

    2013-02-01

    Full Text Available The catalytic properties of nanostructured Au and their physical origin were investigated by using the low-temperature CO oxidation as a test reaction. In order to distinguish between structural effects (structure–activity correlations and bimetallic/bifunctional effects, unsupported nanoporous gold (NPG samples prepared from different Au alloys (AuAg, AuCu by selective leaching of a less noble metal (Ag, Cu were employed, whose structure (surface area, ligament size as well as their residual amount of the second metal were systematically varied by applying different potentials for dealloying. The structural and chemical properties before and after 1000 min reaction were characterized by scanning electron microscopy (SEM, X-ray diffraction (XRD and X-ray photoelectron spectroscopy (XPS. The catalytic behavior was evaluated by kinetic measurements in a conventional microreactor and by dynamic measurements in a temporal analysis of products (TAP reactor. The data reveal a clear influence of the surface contents of residual Ag and Cu species on both O2 activation and catalytic activity, while correlations between activity and structural parameters such as surface area or ligament/crystallite size are less evident. Consequences for the mechanistic understanding and the role of the nanostructure in these NPG catalysts are discussed.

  3. XPS study of Cu-Ni bimetallic catalyst%Cu-Ni双金属催化剂的XPS研究

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    采用XPS方法研究了以不同方式引入Ni的Cu-Ni/Al2O3双金 属催化剂的表面结构及不同处理条件对催化剂表面结构的影响。发现催化剂表面存在表面铝 酸盐物种,且Ni的存在会促进表面铝酸盐物种的生成。催化剂经H2还原处理或经CO2加 氢反应后均要发生表面重构。Ni的存在会影响表面重构过程从而影响催化剂的活性和选择性 ,在所研究的含Ni催化剂上,CO2加氢反应经历了生成双齿表面吸附中间物的过程。%The surface structure of Cu-Ni bimetallic catalysts and its variation with diff erent treatment conditions were studied by XPS techique.The effect of the chemi cal state of Ni before the impregnation of Cu in catalyst preparation on the sur f ace structure and its variation were also investigated.It is found that Cu atom approaches the surface of Al2O3 when it is supported.Surface aluminates a re formed on the surface of the catalysts and the presence of Ni favorites the f ormation of surface aluminates.The surface content of Cu is increased when Ni e x isted in reduced form before the introduction of Cu,while the opposite is true w hen Ni existed in oxidized form before introduction of Cu.Surface reconstructio n is observed when the samples studied are reduced in H2 or treated under CO 2 hydrogenation condition.The hydrogenation of CO2 enriches the surface c ontenrt of Cu species comparing to reduction.After CO2 hydrogenation treat ment,Cu species is observed to migrate to the surface of the catalyst in the abs ence of Ni,while in the presence of Ni surface is remarkably decreased.Bidentat e CO2 adsorptive species with the two O of CO2 cooordinated to metal atom s is a possible intermediate in the hydrogenation of CO2 over Ni containing c atalyst studied.

  4. Effect of surface roughness of cavity preparations on the microleakage of Class V resin composite restorations.

    Science.gov (United States)

    Shook, Larry W; Turner, Edgar W; Ross, Judith; Scarbecz, Mark

    2003-01-01

    This study determined whether surface roughness of the internal walls of a Class V resin composite preparation, using a carbide bur, a medium-grit diamond bur and a fine-grit diamond bur, affected the degree of microleakage of the restoration. The facial and lingual surfaces of 45 non-carious extracted human molars provided 90 samples for evaluation. The specimen surfaces were assigned randomly in equal numbers to one of three groups (n = 30). Conservative Class V composite preparations were made using one of three different burs: a 330-carbide bur, a 330 fine-grit diamond bur or a 330 medium-grit diamond bur (Brasseler USA). After acid etching, PQ1 (Ultradent Products Inc) primer/bonding resin and Vitalescence (Ultradent Products Inc) were applied and cured following the manufacturers' instructions. After minor finishing, the apices of all root surfaces were sealed with Vitrebond (3M), and the unprepared external surfaces were sealed with nail polish to within 1 mm of the restoration margins. The specimens were stored in distilled water at room temperature for 24 hours, then subjected to 1,200 thermocycles at 5 degrees C and 55 degrees C with a 30-second dwell time. After cycling, the teeth were immersed in a 5% solution of methylene blue dye for 12 hours. The molars were invested in clear acrylic casting resin, labeled, then sectioned once vertically approximately midway through the facial and lingual surfaces using a diamond coated saw blade. Microleakage was evaluated using a 10x microscope for the enamel and cementum surfaces and blindly scored by two independent examiners. In all cases, regardless of the examiner, at both the enamel and the dentin margins, the analysis revealed no statistically significant differences in microleakage across bur types. Further results show that dentin margins leaked significantly more than enamel margins for all bur types.

  5. Bimetallic Au/Pd catalyzed aerobic oxidation of alcohols in the poly(ethylene glycol)/CO2 system

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Bimetallic Au/Pd nanoparticles were prepared and used to catalyze oxidation of alcohols in the poly(ethylene glycol) (PEG)/CO2 biphasic system using O2 as the oxidant without adding any base.The catalytic activity of Au/Pd bimetal with different mole ratios was studied using benzyl alcohol as the substrate.It was found that bimetallic Au/Pd nanoparticles with Au:Pd=1:3.5 had higher catalytic activity than monometallic Au,Pd and the bimetallic Au/Pd nanoparticles with other molar ratios.The effect of CO2 pressure on the oxidation of benzyl alcohol and 1-phenylethanol in PEG/CO2 was investigated.It was demonstrated that CO2 pressure could be used to tune the conversion and selectivity of the reactions effectively.α,β-Unsaturated alcohols were also studied and found to be more reactive than benzyl alcohol and 1-phenylethanol.Recycling experiments showed that the Au/Pd/PEG/CO2 catalytic system could be recycled at least four times without reducing the activity.In addition,the catalytic system is clean and the products can be separated easily.

  6. Heterogenized Bimetallic Pd-Pt-Fe3O4 Nanoflakes as Extremely Robust, Magnetically Recyclable Catalysts for Chemoselective Nitroarene Reduction.

    Science.gov (United States)

    Byun, Sangmoon; Song, Yeami; Kim, B Moon

    2016-06-15

    A very simple synthesis of bimetallic Pd-Pt-Fe3O4 nanoflake-shaped alloy nanoparticles (NPs) for cascade catalytic reactions such as dehydrogenation of ammonia-borane (AB) followed by the reduction of nitro compounds (R-NO2) to anilines or alkylamines (R-NH2) in methanol at ambient temperature is described. The Pd-Pt-Fe3O4 NPs were easily prepared via a solution phase hydrothermal method involving the simple one-pot coreduction of potassium tetrachloroplatinate (II) and palladium chloride (II) in polyvinylpyrrolidone with subsequent deposition on commercially available Fe3O4 NPs. The bimetallic Pd-Pt alloy NPs decorated on Fe3O4 NPs provide a unique synergistic effect for the catalysis of cascade dehydrogenation/reduction. Various nitroarene derivatives were reduced to anilines with very specific chemoselectivity in the presence of other reducible functional groups. The bimetallic Pd-Pt-Fe3O4 NPs provide a unique synergistic effect for the catalysis of cascade dehydrogenation/reduction. The nitro reduction proceeded in 5 min with nearly quantitative conversions and yields. Furthermore, the magnetically recyclable nanocatalysts were readily separated using an external magnet and reused up to 250 times without any loss of catalytic activity. A larger scale (10 mmol) reaction was also successfully performed with >99% yield. This efficient, recyclable Pd-Pt-Fe3O4 NPs system can therefore be repetitively utilized for the reduction of various nitro-containing compounds.

  7. Characterization of Au and Bimetallic PtAu Nanoparticles on PDDA-Graphene Sheets as Electrocatalysts for Formic Acid Oxidation

    Science.gov (United States)

    Yung, Tung-Yuan; Liu, Ting-Yu; Huang, Li-Ying; Wang, Kuan-Syun; Tzou, Huei-Ming; Chen, Po-Tuan; Chao, Chi-Yang; Liu, Ling-Kang

    2015-09-01

    Nanocomposite materials of the Au nanoparticles (Au/PDDA-G) and the bimetallic PtAu nanoparticles on poly-(diallyldimethylammonium chloride) (PDDA)-modified graphene sheets (PtAu/PDDA-G) were prepared with hydrothermal method at 90 °C for 24 h. The composite materials Au/PDDA-G and PtAu/PDDA-G were evaluated by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA) for exploring the structural characterization for the electrochemical catalysis. According to TEM results, the diameter of Au and bimetallic PtAu nanoparticles is about 20-50 and 5-10 nm, respectively. X-ray diffraction (XRD) results indicate that both of PtAu and Au nanoparticles exhibit the crystalline plane of (111), (200), (210), and (311). Furthermore, XRD data also show the 2°-3° difference between pristine graphene sheets and the PDDA-modified graphene sheets. For the catalytic activity tests of Au/PDDA-G and PtAu/PDDA-G, the mixture of 0.5 M aqueous H2SO4 and 0.5 M aqueous formic acid was used as model to evaluate the electrochemical characterizations. The catalytic activities of the novel bimetallic PtAu/graphene electrocatalyst would be anticipated to be superior to the previous electrocatalyst of the cubic Pt/graphene.

  8. Characterization of Au and Bimetallic PtAu Nanoparticles on PDDA-Graphene Sheets as Electrocatalysts for Formic Acid Oxidation.

    Science.gov (United States)

    Yung, Tung-Yuan; Liu, Ting-Yu; Huang, Li-Ying; Wang, Kuan-Syun; Tzou, Huei-Ming; Chen, Po-Tuan; Chao, Chi-Yang; Liu, Ling-Kang

    2015-12-01

    Nanocomposite materials of the Au nanoparticles (Au/PDDA-G) and the bimetallic PtAu nanoparticles on poly-(diallyldimethylammonium chloride) (PDDA)-modified graphene sheets (PtAu/PDDA-G) were prepared with hydrothermal method at 90 °C for 24 h. The composite materials Au/PDDA-G and PtAu/PDDA-G were evaluated by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA) for exploring the structural characterization for the electrochemical catalysis. According to TEM results, the diameter of Au and bimetallic PtAu nanoparticles is about 20-50 and 5-10 nm, respectively. X-ray diffraction (XRD) results indicate that both of PtAu and Au nanoparticles exhibit the crystalline plane of (111), (200), (210), and (311). Furthermore, XRD data also show the 2°-3° difference between pristine graphene sheets and the PDDA-modified graphene sheets. For the catalytic activity tests of Au/PDDA-G and PtAu/PDDA-G, the mixture of 0.5 M aqueous H2SO4 and 0.5 M aqueous formic acid was used as model to evaluate the electrochemical characterizations. The catalytic activities of the novel bimetallic PtAu/graphene electrocatalyst would be anticipated to be superior to the previous electrocatalyst of the cubic Pt/graphene.

  9. Thermal Stability of Platinum-Cobalt Bimetallic Nanoparticles: Chemically Disordered Alloys, Ordered Intermetallics, and Core-Shell Structures.

    Science.gov (United States)

    Huang, Rao; Shao, Gui-Fang; Zhang, Yang; Wen, Yu-Hua

    2017-04-12

    Pt-Co bimetallic nanoparticles are promising candidates for Pt-based nanocatalysts and magnetic-storage materials. By using molecular dynamics simulations, we here present a detailed examination on the thermal stabilities of Pt-Co bimetallic nanoparticles with three configurations including chemically disordered alloy, ordered intermetallics, and core-shell structures. It has been revealed that ordered intermetallic nanoparticles possess better structural and thermal stability than disordered alloyed ones for both Pt3Co and PtCo systems, and Pt3Co-Pt core-shell nanoparticles exhibit the highest melting points and the best thermal stability among Pt-Co bimetallic nanoparticles, although their meltings all initiate at the surface and evolve inward with increasing temperatures. In contrast, Co-Pt core-shell nanoparticles display the worst thermal stability compared with the aforementioned nanoparticles. Furthermore, their melting initiates in the core and extends outward surface, showing a typical two-stage melting mode. The solid-solid phase transition is discovered in Co core before its melting. This work demonstrates the importance of composition distribution to tuning the properties of binary nanoparticles.

  10. Preparation of pH-responsive membranes with amphiphilic copolymers by surface segregation method☆

    Institute of Scientific and Technical Information of China (English)

    Yanlei Su; Yuan Liu; Xueting Zhao; Yafei Li; Zhongyi Jiang

    2015-01-01

    Novel pH-responsive membranes were prepared by blending pH-responsive amphiphilic copolymers with pol-yethersulfone (PES) via a nonsolvent-induced phase separation (NIPS) technique. The amphiphilic copolymers bearing Pluronic F127 and poly(methacrylic acid) (PMAA) segments, abbreviated as PMAAn–F127–PMAAn, were synthesized by free radical polymerization. The physical and chemical properties of the blend membranes were evaluated by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectrum, water con-tact angle, Zeta potential and X-ray photoelectron spectroscopy (XPS). The enrichment of hydrophilic PMAA seg-ments on the membrane surfaces was attributed to surface segregation during the membrane preparation process. The blend membranes had significant pH-responsive properties due to the conformational changes of surface-segregated PMAA segments under different pH values of feed solutions. Fluxes of the blend membranes were larger at low pH values of feed solutions than that at high pH values. The pH-responsive ability of the mem-branes was enhanced with the increase of the degree of PMAA near-surface coverage.

  11. Preparation of bovine hemoglobin-imprinted polymer beads via the photografting surface-modified method

    Institute of Scientific and Technical Information of China (English)

    Qingqing GAI; Qiuye LIU; Wenyou LI; Xiwen HE; Langxing CHEN; Yukui ZHANG

    2008-01-01

    Molecularly imprinted polymers (MIPs), based on photografting surface-modified polystyrene beads as matrices, were prepared with acrylamide as the functional monomer, bovine hemoglobin as the template molecule and N, N'-methylene bisacrylamide as the crosslinker in a phosphate buffer. The results of IR, scanning electron microscope (SEM) and elemental analyses demonstrated the formation of a grafting polymer layer on the polysty-rene-bead surface. Subsequent removal of the template left behind cavities on the surface of the polymer matrix with a shape and an arrangement of functional groups having complementary binding sites with the original tem-plate molecule. The adsorption studies showed that the imprinted polymers have a good adsorption capacity and specific recognition for bovine hemoglobin as the template molecule. Our results demonstrated that the polymer prepared via the photografting surface-modified method exhibited better selectivity for the template. Attempts to employ the new method in molecular imprinting techniques may introduce new applications for MIPs and facilitate probable protein separation and purification.

  12. Recent Advances in Facile Synthesis of Bimetallic Nanostructures: An Overview

    Directory of Open Access Journals (Sweden)

    Arash Dehghan Banadaki

    2014-01-01

    Full Text Available Nobel metal nanomaterials with interesting physical and chemical properties are ideal building blocks for engineering and tailoring nanoscale structures for specific technological applications. Bimetallic nanomaterials consisting of magnetic metals and noble metals have attracted much interest for their promising potentials in many fields including magnetic sensors, catalysts, optical detection, and biomedical applications. Particularly, effective control of the size, shape, architecture, and compositional microstructure of metal nanomaterials plays an important role in enhancing their functionality and application potentials, for example, in fuel cells, optical and biomedical sensing. This paper focuses on recent advances in controllable synthesis of bimetallic nanostructured materials. Recent contributions in controllable synthesis of bimetallic nanomaterials with different architectures including nanoparticles, nanowires, nanosheets, or nanotubes and their assemblies are presented in this paper. A wide range of facile synthesis methods are covered herein with high emphasis on wet chemical methods owing to their facility of use, efficacy, and smaller environmental footprint.

  13. Bimetallic Nanoparticles in Alternative Solvents for Catalytic Purposes

    Directory of Open Access Journals (Sweden)

    Trung Dang-Bao

    2017-07-01

    Full Text Available Bimetallic nanoparticles represent attractive catalytic systems thanks to the synergy between both partners at the atomic level, mainly induced by electronic effects which in turn are associated with the corresponding structures (alloy, core-shell, hetero-dimer. This type of engineered material can trigger changes in the kinetics of catalyzed processes by variations on the electrophilicity/nucleophilicity of the metal centers involved and also promote cooperative effects to foster organic transformations, including multi-component and multi-step processes. Solvents become a crucial factor in the conception of catalytic processes, not only due to their environmental impact, but also because they can preserve the bimetallic structure during the catalytic reaction and therefore increase the catalyst life-time. In this frame, the present review focuses on the recent works described in the literature concerning the synthesis of bimetallic nanoparticles in non-conventional solvents, i.e., other than common volatile compounds, for catalytic applications.

  14. Facile Preparation of Efficient WO3 Photocatalysts Based on Surface Modification

    Directory of Open Access Journals (Sweden)

    Min Liu

    2015-01-01

    Full Text Available Tungsten trioxide (WO3 was surface modified with Cu(II nanoclusters and titanium dioxide (TiO2 nanopowders by using a simple impregnation method followed by a physical combining method. The obtained nanocomposites were studied by scanning electron microscope, X-ray photoelectron spectroscopy spectra, UV-visible light spectra, and photoluminescence, respectively. Although the photocatalytic activity of WO3 was negligible under visible light irradiation, the visible light photocatalytic activity of WO3 was drastically enhanced by surface modification of Cu(II nanoclusters and TiO2 nanopowders. The enhanced photocatalytic activity is due to the efficient charge separation by TiO2 and Cu(II nanoclusters functioning as cocatalysts on the surface. Thus, this simple strategy provides a facile route to prepare efficient visible-light-active photocatalysts for practical application.

  15. A novel simple approach to preparation of superhydrophobic surfaces of aluminum alloys

    Science.gov (United States)

    Xie, Degang; Li, Wen

    2011-11-01

    A novel two-step methodology is successfully developed to fabricate superhydrophobic surfaces of aluminum alloys. The essential procedure is that samples are first immersed and etched in a boiling aqueous solution of NaOH for 5 min without preprocessing, and then they are modified for 30 min in an ethanol solution of lauric acid, cheaper and more efficient than the fluorinated silane frequently adopted by other researchers. If the concentration of NaOH solution is larger than 5 g/L, the contact angle of the prepared surfaces will be larger than 150° with a negligible hysteresis. Such a fast, low-cost, and reliable method for superhydrophobic surfaces implies significant promising industrial applications.

  16. Optimal conditions for the preparation of superhydrophobic surfaces on al substrates using a simple etching approach

    Science.gov (United States)

    Ruan, Min; Li, Wen; Wang, Baoshan; Luo, Qiang; Ma, Fumin; Yu, Zhanlong

    2012-07-01

    Many methods have been proposed to develop the fabrication techniques for superhydrophobic surfaces. However, such techniques are still at their infant stage and suffer many shortcomings. In this paper, the superhydrophobic surfaces on an Al substrate were prepared by a simple etching method. Effects of etching time, modifiers, and modification concentration and time were investigated, and optimal conditions for the best superhydrophobicity were studied. It was demonstrated that for etching the aluminum plate in Beck's dislocation, if the etching time was 15 s, modifier was Lauric acid-ethanol solution, and modification concentration and time was 5% and 1.5 h, respectively, the surface exhibited a water contact angle as high as 167.5° and a contact angle hysteresis as low as 2.3°.

  17. Laser-based surface preparation of composite laminates leads to improved electrodes for electrical measurements

    KAUST Repository

    Almuhammadi, Khaled

    2015-10-19

    Electrical impedance tomography (EIT) is a low-cost, fast and effective structural health monitoring technique that can be used on carbon fiber reinforced polymers (CFRP). Electrodes are a key component of any EIT system and as such they should feature low resistivity as well as high robustness and reproducibility. Surface preparation is required prior to bonding of electrodes. Currently this task is mostly carried out by traditional sanding. However this is a time consuming procedure which can also induce damage to surface fibers and lead to spurious electrode properties. Here we propose an alternative processing technique based on the use of pulsed laser irradiation. The processing parameters that result in selective removal of the electrically insulating resin with minimum surface fiber damage are identified. A quantitative analysis of the electrical contact resistance is presented and the results are compared with those obtained using sanding.

  18. Surface and Electrical Properties of NiCr Thin Films Prepared by DC Magnetron Sputtering

    Institute of Scientific and Technical Information of China (English)

    ZHOU Jicheng; TIAN Li; YAN Jianwu

    2008-01-01

    Several batches of NiCr alloy thin films with different thickness were prepared in a multi-targets magnetron sputtering apparatus by changing sputtering time while keeping sputtering target power of Ni and Cr fixed. Then the as-deposited films were characterized by energy-dispersive X-Ray spectrometer (EDX),Atomic Force Microscope (AFM) and four-point probe (FPP) to measure surface grain size, roughness and sheet resistance. The film thickness was measured by Alpha-Step IQ Profilers. The thickness dependence of surface roughness, lateral grain size and resistivity was also studied. The experimental results show that the grain size increases with film thickness and the surface roughness reaches the order of nanometer at all film thickness. The as-deposited film resistivity decreases with film thickness.

  19. Ion-stimulated gas desorption yields and their dependence on the surface preparation of stainless steel

    CERN Document Server

    Mahner, E; Küchler, D; Malabaila, M; Taborelli, M

    2002-01-01

    Ion-induced gas desorption yields were investigated for 4.2 MeV/u lead ions incident on 316 LN stainless steel surfaces. Focussed on a possible application for the Low Energy Ion Ring (LEIR) vacuum system, the influence of surface treatments like chemical etching, electropolishing and gold-coating on the desorption yields was studied with accelerator-type vacuum chambers. The surface composition of similar prepared samples was investigated with X-ray Photoemission Spectroscopy (XPS). Desorption yields for H2, CH4, CO, Ar and CO2, which are of fundamental interest for LEIR and future accelerator applications, are reported as a function of impact angle, ion dose and charge state (+27, +53) of the lead ion beam.

  20. Utilization of microfluidic V-junction device to prepare surface itraconazole adsorbed nanospheres.

    Science.gov (United States)

    Kucuk, Israfil; Ahmad, Zeeshan; Edirisinghe, Mohan; Orlu-Gul, Mine

    2014-09-10

    Itraconazole is widely used as an anti-fungal drug to treat infections. However, its poor aqueous solubility results in low bioavailability. The aim of the present study was to improve the drug release profile by preparing surface itraconazole adsorbed polymethylsilsesquioxane (PMSQ) nanospheres using a V-junction microfluidic (VJM) device. In order to generate nanospheres with rough surface, the process flow rate of perfluorohexane (PFH) was set between 50 and 300 μl min(-1) while the flow rate of PMSQ and itraconazole solution were constant at 300 μl min(-1). Variations in the PFH flow rate enable the controlled size generation of nanospheres. PMSQ nanospheres adsorbing itraconazole were characterized by SEM, FTIR and Zetasizer. The release of itraconazole from PMSQ nanosphere surface was measured using UV spectroscopy. Nanosphere formulations with a range of sphere size (120, 320 and 800 nm diameter) were generated and drug release was studied. 120 nm itraconazole coated PMSQ nanospheres were found to present highest drug encapsulation efficiency and 13% drug loading in a more reproducible manner compared to 320 nm and 800 nm sized nanosphere formulations. Moreover, 120 nm itraconazole coated PMSQ nanospheres (encapsulation efficiency: 88%) showed higher encapsulation efficiency compared to 320 nm (encapsulation efficiency: 74%) and 800 nm (encapsulation efficiency: 62%) sized nanosphere formulations. The itraconazole coated PMSQ nanospheres were prepared continuously at the rate of 2.6 × 10(6) per minute via VJM device. Overall the VJM device enabled the preparation of monodisperse surface itraconazole adsorbed nanospheres with controlled in vitro drug release profile.

  1. Anisotropic surface hole-transport property of triphenylamine-derivative single crystal prepared by solution method

    Science.gov (United States)

    Umeda, Minoru; Katagiri, Mitsuhiko; Shironita, Sayoko; Nagayama, Norio

    2016-12-01

    This paper reports the anisotropic hole transport at the triphenylamine-derivative single crystal surface prepared by a solution method. Triphenylamine derivatives are commonly used in a hole-transport material for organic photoconductors of laser-beam printers, in which the materials are used as an amorphous form. For developing organic photovoltaics using the photoconductor's technology, preparation of a single crystal seems to be a specific way by realizing the high mobility of an organic semiconductor. In this study, a single crystal of 4-(2,2-diphenylethenyl)-N,N-bis(4-methylphenyl)-benzenamine (TPA) was prepared and its anisotropic hole-transport property measured. First, the hole-transport property of the TPA was investigated based on its chemical structure and electrochemical redox characteristics. Next, a large-scale single crystal formation at a high rate was developed by employing a solution method based on its solubility and supersolubility curves. The grown TPA was found to be a single crystal based on the polarization micrograph observation and crystallographic analysis. For the TPA single crystal, an anisotropic surface conduction was found, which was well explained by its molecular stack structure. The measured current in the long-axis direction is one order of magnitude greater than that of amorphous TPA.

  2. Optimization of ultrasonic-assisted preparation of dietary fiber from corn pericarp using response surface methodology.

    Science.gov (United States)

    Wang, Anna; Wu, Ligen; Li, Xiulin

    2013-09-01

    Corn pericarp, which is an industrial waste of corn starch production, is an important source of dietary fiber in cereals, with claimed health benefits. However, they used to be discarded or utilized as animal feed. The application of pre-ultrasound treatment is critical for achieving rapid preparation of desired components from plant materials and for preserving structural and molecular properties of these compounds. Ultrasonic-assisted preparation was used to produce dietary fiber from corn pericarp using response surface methodology. The optimal particle size of corn pericarp (mesh size 40), the ratio of liquid to solid (25 mL g⁻¹), ultrasonic power (180 W) and ultrasonic time (80 min) were determined based on response surface methodology analysis. The interaction effects of particle size of corn pericarp and ultrasonic time had a highlysignificant effect on the yield of dietary fiber, and a significant effect was shown by ultrasonic power and ultrasonic time. The maximum yield of dietary fiber was 86.84%, which agreed closely with the predicted value. Using ultrasonic-assisted preparation, it may be possible to enhance the yield of dietary fiber from corn pericarp. © 2013 Society of Chemical Industry.

  3. Different surface preparation techniques of porcelain repaired with composite resin and fracture resistance

    Directory of Open Access Journals (Sweden)

    Mohd Helmy Khalid Abd Wahab

    2011-01-01

    Full Text Available Background : Porcelain from prosthesis such as crown or bridge can be fractured if exposed to trauma; and, can be repaired at chairside using composite resin. Aim : To investigate the fracture resistance of few techniques of surface preparation in repairing fractured porcelain using composite resin. Materials and Methods : Eighty samples of porcelain blocks were divided into 4 groups for different surface preparations, such as, Cimara repairing kit; porcelain etch kit containing hydrofluoric acid; Panavia F resin cement; and, sandblasting using aluminium oxide, before composite resin (Filtek Z250, 3M ESPE was bonded to the prepared porcelain blocks. Twenty others samples in the control group comprised of pure porcelain blocks. The fracture resistance of each sample was tested using Instron machine (UK. Results : With the exception of the group repaired using hydrofluoric acid (3.04±1.04 Mpa, all the other groups showed significant difference in the fracture resistance values when compared to the control group (3.05 ± 1.42 MPa at P<0.05. Conclusions : Etching of the porcelain blocks with hydrofluoric acid holds promise in the repair of fractured porcelain with composite resin at chairside.

  4. Surface morphology influence on deuterium retention in beryllium films prepared by thermionic vacuum arc method

    Science.gov (United States)

    Anghel, A.; Porosnicu, C.; Badulescu, M.; Mustata, I.; Lungu, C. P.; Sugiyama, K.; Lindig, S.; Krieger, K.; Roth, J.; Nastuta, A.; Rusu, G.; Popa, G.

    2009-01-01

    In a plasma-confinement device, material eroded from plasma facing components will be transported and re-deposited at other locations inside the reaction chamber. Since beryllium from the first wall of the ITER fusion reactor will be eroded, ionized in the scrape-off layer plasma and finally re-deposited on divertor surfaces flowing along the magnetic field, it is important to study the properties of divertor armour materials (C, W) coated with beryllium. By applying different bias voltages (-200 V to +700 V) to the substrates during deposition, the morphology of the obtained films was modified. The films' morphology was characterized by means of AFM and SEM, and it was found that the coatings prepared using negative bias voltage at the substrate during deposition are more compact and have a smoother surface compared to the samples prepared with positive bias voltage. The thickness and composition of each film were measured using Rutherford backscattering spectrometry (RBS). A study of deuterium implantation and retention into the prepared films was performed at IPP Garching in the high current ion source.

  5. Surface modification of silicon-containing fluorocarbon films prepared by plasma-enhanced chemical vapor deposition

    Science.gov (United States)

    Jin, Yoonyoung; Desta, Yohannes; Goettert, Jost; Lee, G. S.; Ajmera, P. K.

    2005-07-01

    Surface modification of silicon-containing fluorocarbon (SiCF) films achieved by wet chemical treatments and through x-ray irradiation is examined. The SiCF films were prepared by plasma-enhanced chemical vapor deposition, using gas precursors of tetrafluoromethane and disilane. As-deposited SiCF film composition was analyzed by x-ray photoelectron spectroscopy. Surface modification of SiCF films utilizing n-lithiodiaminoethane wet chemical treatment is discussed. Sessile water-drop contact angle changed from 95°+/-2° before treatment to 32°+/-2° after treatment, indicating a change in the film surface characteristics from hydrophobic to hydrophilic. For x-ray irradiation on the SiCF film with a dose of 27.4 kJ/cm3, the contact angle of the sessile water drop changed from 95°+/-2° before radiation to 39°+/-3° after x-ray exposure. The effect of x-ray exposure on chemical bond structure of SiCF films is studied using Fourier transform infrared measurements. Electroless Cu deposition was performed to test the applicability of the surface modified films. The x-ray irradiation method offers a unique advantage in making possible surface modification in a localized area of high-aspect-ratio microstructures. Fabrication of a Ti-membrane x-ray mask is introduced here for selective surface modification using x-ray irradiation.

  6. Surface and Adsorption Properties of Activated Carbon Fabric Prepared from Cellulosic Polymer: Mixed Activation Method

    Energy Technology Data Exchange (ETDEWEB)

    Bhati, Surendra; Mahur, J. S.; Choubey, O. N. [Barkatullah Univ., Bhopal (India); Dixit, Mahur Savita [Maulana Azad National Institute of Technology, Bhopla (India)

    2013-02-15

    In this study, activated carbon fabric was prepared from a cellulose-based polymer (viscose rayon) via a combination of physical and chemical activation (mixed activation) processes by means of CO{sub 2} as a gasifying agent and surface and adsorption properties were evaluated. Experiments were performed to investigate the consequence of activation temperature (750, 800, 850 and 925 .deg. C), activation time (15, 30, 45 and 60 minutes) and CO{sub 2} flow rate (100, 200, 300 and 400 mL/min) on the surface and adsorption properties of ACF. The nitrogen adsorption isotherm at 77 K was measured and used for the determination of surface area, total pore volume, micropore volume, mesopore volume and pore size distribution using BET, t-plot, DR, BJH and DFT methods, respectively. It was observed that BET surface area and TPV increase with rising activation temperature and time due to the formation of new pores and the alteration of micropores into mesopores. It was also found that activation temperature dominantly affects the surface properties of ACF. The adsorption of iodine and CCl{sub 4} onto ACF was investigated and both were found to correlate with surface area.

  7. Tribological Behavior of A356/Al2O3 Surface Nanocomposite Prepared by Friction Stir Processing

    Science.gov (United States)

    Mazaheri, Y.; Karimzadeh, F.; Enayati, M. H.

    2014-04-01

    Surface A356 aluminum alloy matrix composites containing micro and nanosized Al2O3 are prepared by a new approach utilizing high-velocity oxy-fuel spraying and friction stir processing (FSP). Optical and scanning electron microscopy, microhardness, and wear tests were used to characterize the surface composites. Results indicated that, the presence of Al2O3 in matrix can improve the mechanical properties of specimens. The microhardness of surface composites containing micro and nanosized Al2O3 were 89.8 ± 2.6 HV and 109.7 ± 2.5 HV, respectively, which were higher than those for the as-received (79.6 ± 1.1 HV) and the FSPed A356-T6 with no alumina powder (66.8 ± 0.9 HV). Surface composites revealed low friction coefficients and wear rates, which were significantly lower than those obtained for substrate. The wear mass losses of the as-received, the FSPed, and surface micro and nanocomposite specimens after 500-m sliding distance were 50.5, 55.6, 31, and 17.2 mg, respectively. Scanning electron microscopy tests revealed different wear mechanisms on the surface of the wear test specimens.

  8. Microbial synthesis of bimetallic PdPt nanoparticles for catalytic reduction of 4-nitrophenol.

    Science.gov (United States)

    Tuo, Ya; Liu, Guangfei; Dong, Bin; Yu, Huali; Zhou, Jiti; Wang, Jing; Jin, Ruofei

    2017-02-01

    Bimetallic nanoparticles are generally believed to have improved catalytic activity and stability due to geometric and electronic changes. In this work, biogenic-Pd (bio-Pd), biogenic-Pt (bio-Pt), and biogenic-PdPt (bio-PdPt) nanoparticles were synthesized by Shewanella oneidensis MR-1 in the absence or presence of quinone. Compared with direct microbial reduction process, the addition of anthraquinone-2,6-disulfonate (AQDS) could promote the reduction efficiency of Pd(II) or/and Pt(IV) and result in decrease of particles size. All kinds of nanoparticles could catalyze 4-nitrophenol reduction by NaBH4 and their catalytic activities took the following order: bio-PdPt (AQDS) ∼ bio-PdPt > bio-Pd (AQDS) > bio-Pd > bio-Pt (AQDS) ∼ bio-Pt. Moreover, the bio-PdPt (AQDS) nanoparticles could be reused for 6 cycles. We believe that this simple and efficient biosynthesis approach for synthesizing bimetallic bio-PdPt nanocatalysts is important for preparing active and stable catalysts.

  9. Electrospun carbon nanofibers decorated with Ag-Pt bimetallic nanoparticles for selective detection of dopamine.

    Science.gov (United States)

    Huang, Yunpeng; Miao, Yue-E; Ji, Shanshan; Tjiu, Weng Weei; Liu, Tianxi

    2014-08-13

    Electrospun nanoporous carbon nanofibers (pCNFs) decorated with Ag-Pt bimetallic nanoparticles have been successfully synthesized by combining template carbonization and seed-growth reduction approach. Porous-structured polyacrylonitrile (PAN) nanofibers (pPAN) were first prepared by electrospinning PAN/polyvinylpyrrolidone (PVP) blend solution, followed by subsequent water extraction and heat treatment to obtain pCNFs. Ag-Pt/pCNFs were then obtained by using pCNFs as support for bimetallic nanoparticle loading. Thus, the obtained Ag-Pt/pCNFs were used to modify glassy carbon electrode (GCE) for selective detection of dopamine (DA) in the presence of uric acid (UA) and ascorbic acid (AA). This novel sensor exhibits fast amperometric response and high sensitivity toward DA with a wide linear concentration range of 10-500 μM and a low detection limit of 0.11 μM (S/N = 3), wherein the interference of UA and AA can be eliminated effectively.

  10. Light alkane (mixed feed selective dehydrogenation using bi-metallic zeolite supported catalyst

    Directory of Open Access Journals (Sweden)

    Zeeshan Nawaz

    2009-12-01

    Full Text Available Light alkanes are the important intermediates of many refinery processes and their catalytic dehydrogenation gives corresponding alkenes. The aim behind this experimentation is to investigate reaction behavior of mixed alkanes during direct catalytic dehydrogenation and emphasis has been given to enhance propene. Bi-metallic zeolite supported catalyst Pt-Sn/ZSM-5 was prepared by sequentional impregnation method and characterized by BET, EDS and XRD. Direct dehydrogenation reaction is highly endothermic and its conversion is thermodynamically limited. Results showed that the increase in temperature increases the conversion to some extent but there is no overall effect on selectivity of propene. Increase in time-on-stream (TOS remarkably improves propene selectivity at the expense of lower conversion. The performances of bi-metallic zeolite based catalyst largely affected by coke deposition. The presence of butane and ethane adversely affected propane conversion. Optimum propene selectivity is about 48 %, obtained at 600 oC and time-on-stream 10 h.

  11. Bimetallic PtxCoy nanoparticles with curved faces for highly efficient hydrogenation of cinnamaldehyde.

    Science.gov (United States)

    Gu, Yan; Zhao, Yonghui; Wu, Panpan; Yang, Bo; Yang, Nating; Zhu, Yan

    2016-06-07

    The control of the curved structure of bimetallic nanocrystals is a challenge, due to the rate differential for atom deposition and surface diffusion of alien atomic species on specific crystallographic planes of seeds. Herein, we report how to tune the degree of concavity of bimetallic PtxCoy concave nanoparticles using carboxylic acids as surfactants with an oleylamine system, leading to the specific crystallographic planes being exposed. The terminal carboxylic acids with a bridge ring or a benzene ring serving as structure regulators could direct the formation of curved faces with exposed high-index facets, and long-chain saturated fatty acids favored the production of curved faces with exposed low-index facets, while long-chain olefin acids alone benefited the formation of a flat surface with exposed low-index planes. Furthermore, these PtxCoy particles with curved faces displayed superior catalytic behaviour to cinnamaldehyde hydrogenation when compared with PtxCoy with flat faces. PtxCoy nanoparticles with curved faces exhibited over 6-fold increase in catalytic activity compared to PtxNiy nanoparticles with curved faces, and near 40-fold activity increase was observed in comparison with PtxFey nanoparticles with curved faces.

  12. Preparation of clean surfaces and Se vacancy formation in Bi2Se3 by ion bombardment and annealing

    Science.gov (United States)

    Zhou, Weimin; Zhu, Haoshan; Valles, Connie M.; Yarmoff, Jory A.

    2017-08-01

    Bismuth Selenide (Bi2Se3) is a topological insulator (TI) with a structure consisting of stacked quintuple layers. Single crystal surfaces are commonly prepared by mechanical cleaving. This work explores the use of low energy Ar+ ion bombardment and annealing (IBA) as an alternative method to produce reproducible and stable Bi2Se3 surfaces under ultra-high vacuum (UHV). It is found that a clean and well-ordered surface can be prepared by a single cycle of 1 keV Ar+ ion bombardment and 30 min of annealing. Low energy electron diffraction (LEED) and detailed low energy ion scattering (LEIS) measurements show no differences between IBA-prepared surfaces and those prepared by in situ cleaving in UHV. Analysis of the LEED patterns shows that the optimal annealing temperature is 450 °C. Angular LEIS scans reveal the formation of surface Se vacancies when the annealing temperature exceeds 520 °C.

  13. Bimetallic Ni/Pd finite systems: Structure and thermodynamics of bimetallic Ni/Pd nanostructures in two and three dimensions

    Energy Technology Data Exchange (ETDEWEB)

    Nieves-Torres, Stephanie [Department of Chemistry, University of Puerto Rico at Mayagueez, Mayagueez 00681 (Puerto Rico); Mo, Elizabeth [Department of Chemistry, Lehman College-CUNY, Bronx, NY 10468 (United States); Lopez, Gustavo E., E-mail: glopez@uprm.edu [Department of Chemistry, University of Puerto Rico at Mayagueez, Mayagueez 00681 (Puerto Rico); Department of Chemistry, Lehman College-CUNY, Bronx, NY 10468 (United States)

    2011-09-15

    Highlights: {yields} Structure and thermodynamic of Ni/Pd bimetallic clusters as a function of composition. {yields} Melting and low temperature order-disorder transitions in Ni/Pd bimetallic clusters. {yields} Implementation of efficient classical Monte Carlo techniques. - Abstract: By implementing replica-exchange Monte Carlo simulations within the multihistogram reweighting techniques, the structural and thermodynamic changes in bimetallic nickel-palladium nanostructured systems were studied as a function of composition. Specifically, two- and three-dimensional clusters composed of seven and thirteen atoms, respectively, were described using the embedded atom potential. The lowest energy equilibrium structures were determined, and associated to the degree of mixing in the material. In all cases, melting and order-disorder transitions were revealed by calculating the average constant volume heat capacity as a function of temperature. The change in Helmholtz free energy for the order-disorder transition was determined as a function of composition for each system.

  14. The effect of surface preparation on the behaviour of double strap adhesive joints with thick steel adherents

    DEFF Research Database (Denmark)

    Anyfantis, K.N.; Tsouvalis, N.G.

    2009-01-01

    for preparing the bonding surfaces are investigated, namely grit blasting (GB) and simple sandpaper (SP). The behaviour of the joints, in terms of the force-displacement and strains-displacement responses was monitored and compared for both cases. The joints with SP surface preparation exhibited slightly lower...... stiffness and lower strength than the joints with GB surface preparation, while the latter failed at a lower displacement. In both cases, failure initiated at the free edges of the joints and the dominating failure mode was interfacial. In addition to the above experimental measurements, results are also...

  15. Method for the preparation of high surface area high permeability carbons

    Science.gov (United States)

    Lagasse, R.R.; Schroeder, J.L.

    1999-05-11

    A method for preparing carbon materials having high surface area and high macropore volume to provide high permeability. These carbon materials are prepared by dissolving a carbonizable polymer precursor, in a solvent. The solution is cooled to form a gel. The solvent is extracted from the gel by employing a non-solvent for the polymer. The non-solvent is removed by critical point drying in CO{sub 2} at an elevated pressure and temperature or evaporation in a vacuum oven. The dried product is heated in an inert atmosphere in a first heating step to a first temperature and maintained there for a time sufficient to substantially cross-link the polymer material. The cross-linked polymer material is then carbonized in an inert atmosphere. 3 figs.

  16. Method for the preparation of high surface area high permeability carbons

    Energy Technology Data Exchange (ETDEWEB)

    Lagasse, Robert R. (Albuquerque, NM); Schroeder, John L. (Albuquerque, NM)

    1999-05-11

    A method for preparing carbon materials having high surface area and high macropore volume to provide high permeability. These carbon materials are prepared by dissolving a carbonizable polymer precursor, in a solvent. The solution is cooled to form a gel. The solvent is extracted from the gel by employing a non-solvent for the polymer. The non-solvent is removed by critical point drying in CO.sub.2 at an elevated pressure and temperature or evaporation in a vacuum oven. The dried product is heated in an inert atmosphere in a first heating step to a first temperature and maintained there for a time sufficient to substantially cross-link the polymer material. The cross-linked polymer material is then carbonized in an inert atmosphere.

  17. Preparation and surface encapsulation of hollow TiO nanoparticles for electrophoretic displays

    Energy Technology Data Exchange (ETDEWEB)

    Zhao Qian [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Tan Tingfeng, E-mail: tantingfeng@sina.com [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Department of Materials Science and Engineering, Tianjin Institute of Urban Construction, Tianjin 300384 (China); Qi Peng [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Wang Shirong, E-mail: wangshirong@tju.edu.cn [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Bian Shuguang [High Technology Research and Development Center, Ministry of Science and Technology, Beijing 100044 (China); Li Xianggao; An Yong; Liu Zhaojun [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China)

    2011-02-01

    Hollow black TiO nanosparticles were obtained via deposition of inorganic coating on the surface of hollow core-shell polymer latex with Ti(OBu){sub 4} as precursor and subsequent calcination in ammonia gas. Hollow TiO particles were characterized by scanning electron microscope, transmission electronic microscopy, X-ray diffraction, and thermogravimetric analysis. Encapsulation of TiO via dispersion polymerization was promoved by pretreating the pigments with 3-(trimethoxysilyl) propyl methacrylate, making it possible to prepare hollow TiO-polymer particles. When St and DVB were used as polymerization monomer, hollow TiO-polymer core-shell particles came into being via dispersion polymerization, and the lipophilic degree is 28.57%. Glutin-arabic gum microcapsules containing TiO-polymer particles electrophoretic liquid were prepared using via complex coacervation. It was founded that hollow TiO-polymer particles had enough electrophoretic mobility after coating with polymer.

  18. Study of the Preparation, Characterization, and Sizing Performance of Modified Collagen Surface Sizing Agent

    Directory of Open Access Journals (Sweden)

    Xuechuan Wang

    2014-01-01

    Full Text Available In this work, a surface sizing agent for paper was prepared by the emulsion polymerization method, in which the collagen extracted from leather shavings was modified. The product was characterized using Fourier Transform-Infrared Spectroscopy (FT-IR, Transmission Electron Microscopy (TEM, X-ray Diffraction (XRD, Energy Dispersive X-ray detector (EDX, and atomic absorption spectrophotometry. Corrugated papers were used as models. The synergy between modified collagen sizing emulsion and two commercial synthetic sizing agents was studied. Finally, the morphology of the papers before and after being treated was observed by Scanning Electron Microscopy (SEM. The results indicated that the sizing agent could be prepared using collagen as a raw material, which not only can alleviate a pollution problem in the leather industry, but also provide a novel alternative sizing agent for the paper industry, providing considerable economic, social, and environmental benefits to both industries.

  19. Preparation of miniantibodies to Azospirillum brasilense Sp245 surface antigens and their use for bacterial detection.

    Science.gov (United States)

    Dykman, Lev A; Staroverov, Sergei A; Guliy, Olga I; Ignatov, Oleg V; Fomin, Alexander S; Vidyasheva, Irina V; Karavaeva, Olga A; Bunin, Viktor D; Burygin, Gennady L

    2012-01-01

    This article reports the first preparation of miniantibodies to Azospirillum brasilense Sp245 surface antigens by using a combinatorial phage library of sheep antibodies. The prepared phage antibodies were used for the first time for lipopolysaccharide and flagellin detection by dot assay, electro-optical analysis of cell suspensions, and transmission electron microscopy. Interaction of A. brasilense Sp245 with antilipopolysaccharide and antiflagellin phage-displayed miniantibodies caused the magnitude of the electro-optical signal to change considerably. The electro-optical results were in good agreement with the electron microscopic data. This is the first reported possibility of employing phage-displayed miniantibodies in bacterial detection aided by electro-optical analysis of cell suspensions.

  20. High surface area activated carbon prepared from cassava peel by chemical activation.

    Science.gov (United States)

    Sudaryanto, Y; Hartono, S B; Irawaty, W; Hindarso, H; Ismadji, S

    2006-03-01

    Cassava is one of the most important commodities in Indonesia, an agricultural country. Cassava is one of the primary foods in our country and usually used for traditional food, cake, etc. Cassava peel is an agricultural waste from the food and starch processing industries. In this study, this solid waste was used as the precursor for activated carbon preparation. The preparation process consisted of potassium hydroxide impregnation at different impregnation ratio followed by carbonization at 450-750 degrees C for 1-3 h. The results revealed that activation time gives no significant effect on the pore structure of activated carbon produced, however, the pore characteristic of carbon changes significantly with impregnation ratio and carbonization temperature. The maximum surface area and pore volume were obtained at impregnation ratio 5:2 and carbonization temperature 750 degrees C.

  1. Electrodeposition of photocatalytic TiO2 film on surface of alumina prepared by anodic oxidation

    Institute of Scientific and Technical Information of China (English)

    ZHANG Xin-yu; CHEN Tie-qun

    2004-01-01

    A new electrochemical method to prepare photocatalytic TiO2 thin film was developed, by which the TiO2 was electrodeposited on surface of alumina by AC electrolysis in solution consisting of K2 [TiO(C2O4 )2] and C2H2O4. The deposited TiO2 thin film was primarily characterized by X-ray diffraction (XRD), scanning electronic microscopy (SEM) and energy dispersive spectrum (EDS) methods. The photocatalytic properties of this film were also studied by the photocatalytic degradation of methyl orange. The results show that the TiO2 film electrodeposited by this method is mainly in amorphous and with a little crystalline component mixed anatase and rutile. The surface of the alumina prepared by anodic oxidation is porous and the TiO2 electrodeposited on it is scattered and incompact. TiO2 thin film fixed on the surface of alumina shows photocatalytic activity to the degradation of methyl orange.

  2. Honeycomb-patterned films of polystyrene/poly(ethylene glycol): Preparation, surface aggregation and protein adsorption

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Highly ordered honeycomb-patterned polystyrene (PS)/poly(ethylene glycol) (PEG) films were prepared by a water-assisted method using an improved setup, which facilitated the formation of films with higher regularity, better reproducibility, and larger area of honeycomb structures. Surface aggregation of hydrophilic PEG and adsorption of bovine serum albumin (BSA) on the honeycomb-patterned films were investigated. Field emission scanning electron microscopy (FESEM) and atomic force microscopy (AFM) were used to observe the surface morphologies of the films before and after being rinsed with water. As confirmed by the FESEM images and the AFM phase images, PEG was enriched in the pores and could be gradually removed by water. The adsorption of fluorescence-labeled BSA on the films was studied in visual form using laser scanning confocal microscopy. Results clearly demonstrated that the protein-resistant PEG was selectively enriched in the pores. This water-assisted method may be a latent tool to prepare honeycomb-patterned biofunctional surfaces.

  3. Design and preparation of matrine surface-imprinted material and studies on its molecule recognition selectivity.

    Science.gov (United States)

    Lei, Qingjuan; Gao, Baojiao; Zhang, Dandan

    2016-01-01

    A matrine molecule surface-imprinted material was designed and prepared using an effective surface-imprinting technique developed by our group, and its molecular recognition performance and mechanism were investigated in depth. Monomer glycidyl methacrylate (GMA) was first graft-polymerized on the surfaces of micron-sized silica gel particles in surface-initiated graft polymerization manner, obtaining the grafted particles PGMA/SiO(2) with high grafting degree. Subsequently, the ring-opening reaction of the epoxy groups of the grafted macromolecules PGMA with 5-aminosalicylic acid (5-ASA) was carried out, resulting in the functional grafted particle SA-PGMA/SiO(2), on whose surfaces salicylic acid as functional group was chemically bonded. By right of the mutual strong secondary bond forces, electrostatic interaction and hydrogen bonding, SA-PGMA/SiO(2) particles produced strong adsorption for matrine. Finally, with this strong adsorption, matrine molecule surface imprinting was carried out on the surfaces of SA-PGMA/SiO(2) particles with ethylene glycol diglycidyl ether as cross-linking agent, resulting in the matrine molecule surface-imprinted material MIP-SAP/SiO(2). The binding characteristic of MIP-SAP/SiO(2) toward matrine was investigated in depth with both batch and column methods and using oxymatrine and cytisine as two contrast alkaloids. The experimental results show that MIP-SAP/SiO(2) has special recognition selectivity and excellent binding affinity for matrine. Relative to oxymatrine and cytisine, the selectivity coefficients of MIP-SAP/SiO(2) for matrine are 5.66 and 11.17, respectively.

  4. Cost-Benefit Analysis For Alternative Low-Emission Surface Preparation/ Depainting Technologies for Structural Steel

    Science.gov (United States)

    Lewis, Pattie

    2007-01-01

    Stennis Space Center (SSC), Kennedy Space Center (KSC) and Air Force Space Command (AFSPC) identified particulate emissions and waste generated from the depainting process of steel structures as hazardous materials to be eliminated or reduced. A Potential Alternatives Report, Potential Alternatives Report for Validation of Alternative Low Emission Surface Preparation/Depainting Technologies for Structural Steel, provided a technical analyses of identified alternatives to the current coating removal processes, criteria used to select alternatives for further analysis, and a list of those alternatives recommended for testing. The initial coating removal alternatives list was compiled using literature searches and stakeholder recommendations. The involved project participants initially considered approximately 13 alternatives. In late 2003, core project members selected the following depainting processes to be further evaluated: (1) Plastic Blast Media-Quickstrip(R)-A. (2) Hard Abrasive-Steel-Magic(R). (3) Sponge Blasting-Sponge-Jet(R). (4) Liquid Nitrogen-NItroJet(R). (5) Mechanical Removal with Vacuum Attachment-DESCO and OCM Clean-Air (6) Laser Coating Removal Alternatives were tested in accordance with the Joint Test Protocol for Validation of Alternative Low-Emission Surface Preparation/Depainting Technologies for Structural Steel, and the Field Evaluation Test Plan for Validation of Alternative Low-Emission Surface Preparation/Depainting Technologies for Structural Steel. Results of the testing are documented in the Joint Test Report. This Cost-Benefit Analysis (CBA) focuses on the three alternatives (Quickstrip(R)-A, SteelMagic (R), and Sponge-Jet(R)) that were considered viable alternatives for large area operations based on the results of the field demonstration and lab testing. This CBA was created to help participants determine if implementation of the candidate alternatives is economically justified. Each of the alternatives examined reduced Environmental

  5. Preparation and characterization of poly(indole-3-carboxaldehyde) film at the glassy carbon surface

    Energy Technology Data Exchange (ETDEWEB)

    Deletioglu, Didem [Mustafa Kemal University, Faculty of Arts and Science, Department of Chemistry, Antakya (Turkey); Hasdemir, Erdogan, E-mail: hasdemir@gazi.edu.t [Gazi University, Faculty of Arts and Science, Department of Chemistry, Ankara (Turkey); Solak, Ali Osman [Ankara University, Faculty of Science, Department of Chemistry, Ankara (Turkey); Ustuendag, Zafer [Dumlupinar University, Faculty of Arts and Science, Department of Chemistry, Kuetahya (Turkey); Guezel, Remziye [Dicle University, Faculty of Arts and Sciences, Department of Chemistry, Diyarbakir (Turkey)

    2010-11-01

    Indole-3-carboxaldehyde (In3C) monomer was oxidized by electrochemical methods at the glassy carbon (GC) electrode in 0.05 M tetrabutylammonium tetrafluoroborate in acetonitrile, with the aim to prepare a modified electrode. Modification was performed using cyclic voltammetry (CV) scanning from 0.0 V to 2.0 V at a scan rate of 50 mV s{sup -1} for 10 cycles in 1 mM In3C monomer solution. The modified GC surface (In3C-GC) was characterized by CV response of potassium ferricyanide and ferrocene redox probes as well as by the electrochemical impedance spectroscopy. The modified surface was analyzed by reflection-absorption infrared spectroscopy and compared with the spectrum of the monomeric In3C. Elemental composition of the surface was determined by X-ray photoelectron spectroscopy. Contact angle measurements was also performed to check the changes in hydrophobic character of the bare GC and compared to that of In3C-GC surface. Thickness of the oligomeric/polymeric film was investigated by ellipsometric measurements and a surface confined polymerization mechanism was proposed.

  6. Preparation of multi-functional superhydrophobic lanthanum surface on carbon steel via facile electrochemical method

    Science.gov (United States)

    Chen, Xi; He, Yi; Fan, Yi; Yang, Qiangbin; Li, Han

    2016-12-01

    We have constructed a superhydrophobic surface with lanthanum palmitate on carbon steel via a facile one-step electrodeposition. The morphology and chemical composition of the superhydrophobic surface were characterized by field-emission scanning electron microscopy with attached energy dispersive X-ray spectrum, Fourier transform infrared spectra and X-ray photoelectron spectroscopy, respectively. The as-prepared surface with hierarchical structure has a largest contact angle of 160° ± 0.5° and a lowest sliding angle of 2° ± 0.5°. We found that both high electrodeposition potential and high concentrations lanthanum nitrate can accelerate the formation of superhydrophobic film. The electrochemical measurements demonstrated that the superhydrophobic surface exhibited excellent anti-corrosion performance in 3.5 wt% NaCl solution. Moreover, we also investigated the chemical stability, self-cleaning and oil/water separation of the superhydrophobic film. We believe that the facile fabrication method provides a promising strategy to fabricate multi-functional superhydrophobic surface with lanthanide series rare-earth elements on kinds of substrates.

  7. Microleakage in conservative cavities varying the preparation method and surface treatment

    Directory of Open Access Journals (Sweden)

    Juliana Abdallah Atoui

    2010-08-01

    Full Text Available OBJECTIVE: To assess microleakage in conservative class V cavities prepared with aluminum-oxide air abrasion or turbine and restored with self-etching or etch-and-rinse adhesive systems. Materials and Methods: Forty premolars were randomly assigned to 4 groups (I and II: air abrasion; III and IV: turbine and class V cavities were prepared on the buccal surfaces. Conditioning approaches were: groups I/III - 37% phosphoric acid; groups II/IV - self-priming etchant (Tyrian-SPE. Cavities were restored with One Step Plus/Filtek Z250. After finishing, specimens were thermocycled, immersed in 50% silver nitrate, and serially sectioned. Microleakage at the occlusal and cervical interfaces was measured in mm and calculated by a software. Data were subjected to ANOVA and Tukey's test (α=0.05. RESULTS: Marginal seal provided by air abrasion was similar to high-speed handpiece, except for group I. There was SIGNIFICANT difference between enamel and dentin/cementum margins for to group I and II: air abrasion. The etch-and-rinse adhesive system promoted a better marginal seal. At enamel and dentin/cementum margins, the highest microleakage values were found in cavities treated with the self-etching adhesive system. At dentin/cementum margins, high-speed handpiece preparations associated with etch-and-rinse system provided the least dye penetration. CONCLUSION: Marginal seal of cavities prepared with aluminum-oxide air abrasion was different from that of conventionally prepared cavities, and the etch-and-rinse system promoted higher marginal seal at both enamel and dentin margins.

  8. Hydrogen Production on Ag-Pd/TiO2 Bimetallic Catalysts: Is there a Combined Effect of Surface Plasmon Resonance with Schottky Mechanism on the Photo-Catalytic Activity?

    KAUST Repository

    Nadeem, Muhammad A.

    2017-03-28

    Despite many observations that plasmonics can enhance photocatalytic reactions, their relative role in the overall reaction rate is not thoroughly investigated. Here we report that silver nanoparticles contribution in the reaction rate by its plasmonic effect is negligible when compared to that of Pd (Schottky effect). To conduct the study a series of Ag−Pd/TiO2 catalysts have been prepared, characterized and tested for H2 production from water in the presence of an organic sacrificial agent. Pd was chosen as a standard high work function metal needed for the Schottky junction to pump away electrons from the conduction band of the semiconductor and Ag (whose work function is ca. 1 eV lower than that of Pd) for its high plasmonic resonance response at the edge of the bandgap of TiO2. While H2 production rates showed linear dependency on plasmonic response of Ag in the Pd−Ag series, the system performed less than that of pure Pd. In other words, the plasmonic contribution of Ag in the Ag−Pd/TiO2 catalyst for hydrogen production, while confirmed using different excitation energies, is small. Therefore, the “possible” synergistic effect of plasmonic (in the case of Ag) and Schottky-mechanism (in the case of Pd) is minor when compared to that of Schottky-effect alone.

  9. Polymer Film Supported Bimetallic Au-Ag Catalysts for Electrocatalytic Oxidation of Ammonia Borane in Alkaline Media

    Institute of Scientific and Technical Information of China (English)

    Şükriye Ulubay Karabiberoglu; ÇagrCeylan Koçak; Süleyman Kocak; Zekerya Dursun

    2016-01-01

    Ammonia borane is widely used in most areas including fuel cell applications. The present paper describes electrochemical behavior of ammonia borane in alkaline media on the poly(p-aminophenol) film modified with Au and Ag bimetallic nanoparticles. The glassy carbon electrode was firstly covered with polymeric film electrochemically and then, Au, Ag, and Au–Ag nanoparticles were deposited on the polymeric film, respectively. The surface morphology and chemical composition of these electrodes were examined by scanning electron microscopy, transmission electron microscopy, electrochemical impedance spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. It was found that alloyed Au–Ag bimetallic nanoparticles are formed. Electrochemical measurements indicate that the developed electrode modified by Au–Ag bimetallic nanoparticles exhibit the highest electrocatalytic activity for ammonia borane oxidation in alkaline media. The rotating disk electrode voltammetry demonstrates that the developed electrode can catalyze almost six-electron oxidation pathway of ammonia borane. Our results may be attractive for anode materials of ammonia borane fuel cells under alkaline conditions.

  10. PdPt bimetallic nanoparticles enabled by shape control with halide ions and their enhanced catalytic activities.

    Science.gov (United States)

    Zhang, Jinfeng; Wan, Lei; Liu, Lei; Deng, Yida; Zhong, Cheng; Hu, Wenbin

    2016-02-21

    In this study, a new and convenient one step approach is described for synthesizing shape controlled PdPt bimetallic nanoparticles. It is found that the resultant morphologies of these PdPt nanoparticles can be well controlled by simply altering the participation of different halide ions that serve as shape controlling agents in the reaction solution. The dendritic core-shell PdPt bimetallic nanoparticles generated with Pt atoms adopt usual island growth pattern in the presence of Cl(-) ions, whereas the introduction of Br(-) ions with a relatively strong adsorption effect facilitate the formation of a layered core-shell structure due to the layered growth mode of Pt atoms on the exterior surface of the central Pd core. Moreover, the stronger adsorption function of I(-) ions and the resulting fast atomic diffusion promoted the generation of mesoporous core-shell PdPt bimetallic nanoparticles with many pore channels. In addition, the size of these synthesized PdPt nanoparticles exhibited a significant dependence on the concentration of the halide ions involved. Due to their specific structural features and synergistic effects, these PdPt catalysts exhibited shape-dependent catalytic performance and drastically enhanced electrocatalytic activities relative to that of commercial Pt black and Pt/C toward methanol oxidation.

  11. Catalytic dechlorination of 2,4-dichlorophenol by Pd/Fe bimetallic nanoparticles in the presence of humic acid.

    Science.gov (United States)

    Zhang, Zhen; Shen, Qiaohui; Cissoko, Naman; Wo, Jingjing; Xu, Xinhua

    2010-10-15

    Pd/Fe bimetallic nanoparticles were synthesized for treatment of 2,4-dichlorophenol (2,4-DCP) in the presence of humic acid (HA), in order to understand their applicability for in situ remediation of groundwater. In this case, 2,4-DCP was catalytically dechlorinated to form the final products--phenol (P) via two intermediates, namely o-chlorophenol (o-CP) and p-chlorophenol (p-CP). We demonstrated that the carbon mass balances during the dechlorination were in the range of 82-91%, and other carbons were absorbed on the surface of Pd/Fe bimetallic nanoparticles. Our results suggest the dechlorination reaction of 2,4-DCP by Pd/Fe bimetallic nanoparticles in the presence of HA followed pseudo-first-order kinetics. HA competed for reaction sites on the Pd/Fe bimetallic nanoparticles with 2,4-DCP, and thus reduced the efficiency and rate of the dechlorination of 2,4-DCP. Efficiencies of dechlorination and phenol formations increased significantly as the Pd content increased from 0.10 wt.%, 0.15 wt.% to 0.20 wt.%, the removal percentage of 2,4-DCP increased from 70.4%, 98.4% to 99.4% within 300 min, respectively, the nitrate (NO(3)(-)) content in water also has a significant impact on 2,4-DCP dechlorination efficiency. Our results show that no other intermediates were generated besides Cl(-), o-CP, p-CP and phenol during the catalytic dechlorination of 2,4-DCP. 2010 Elsevier B.V. All rights reserved.

  12. Textured surface structures formed using new techniques on transparent conducting Al-doped zinc oxide films prepared by magnetron sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Minami, Tadatsugu [Optoelectronic Device System R& D Center, Kanazawa Institute of Technology, Nonoichi, Ishikawa 921-8501 (Japan); Miyata, Toshihiro, E-mail: tmiyata@neptune.kanazawa-it.ac.jp [Optoelectronic Device System R& D Center, Kanazawa Institute of Technology, Nonoichi, Ishikawa 921-8501 (Japan); Uozaki, Ryousuke [Optoelectronic Device System R& D Center, Kanazawa Institute of Technology, Nonoichi, Ishikawa 921-8501 (Japan); Sai, Hitoshi; Koida, Takashi [Research Center for Photovoltaics, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 305-8568 (Japan)

    2016-09-01

    Surface-textured Al-doped ZnO (AZO) films formed using two new techniques based on magnetron sputtering deposition were developed by optimizing the light scattering properties to be suitable for transparent electrode applications in thin-film silicon solar cells. Scrambled egg-like surface-textured AZO films were prepared using a new texture formation technique that post-etched pyramidal surface-textured AZO films prepared under deposition conditions suppressing c-axis orientation. In addition, double surface-textured AZO films were prepared using another new texture formation technique that completely removed, by post-etching, the pyramidal surface-textured AZO films previously prepared onto the initially deposited low resistivity AZO films; simultaneously, the surface of the low resistivity films was slightly etched. However, the obtained very high haze value in the range from the near ultraviolet to visible light in the scrambled egg-like surface-textured AZO films did not contribute significantly to the obtainable photovoltaic properties in the solar cells fabricated using the films. Significant light scattering properties as well as a low sheet resistance could be achieved in the double surface-textured AZO films. In addition, a significant improvement of external quantum efficiency in the range from the near ultraviolet to visible light was achieved in superstrate-type n-i-p μc-Si:H solar cells fabricated using a double surface-textured AZO film prepared under optimized conditions as the transparent electrode. - Highlights: • Double surface-textured AZO films prepared using a new texture formation technique • Extensive light scattering properties with low sheet resistance achieved in the double surface-textured AZO films • Improved external quantum efficiency of μc-Si:H solar cells using a double surface-textured AZO film.

  13. The Effect of Nylon and Polyester Peel Ply Surface Preparation on the Bond Quality of Composite Laminates

    Science.gov (United States)

    Moench, Molly K.

    The preparation of the surfaces to be bonded is critical to the success of composite bonds. Peel ply surface preparation is attractive from a manufacturing and quality assurance standpoint, but is a well known example of the extremely system-specific nature of composite bonds. This study examined the role of the surface energy, morphology, and chemistry left by peel ply removal in resulting bond quality. It also evaluated the use of contact angle surface energy measurement techniques for predicting the resulting bond quality of a prepared surface. The surfaces created by preparing three aerospace fiber-reinforced composite prepregs were compared when prepared with a nylon vs a polyester peel ply. The prepared surfaces were characterized with contact angle measurements with multiple fluids, scanning electron microscopy (SEM), and x-ray electron spectroscopy. The laminates were bonded with aerospace grade film adhesives. Bond quality was assessed via double cantilever beam testing followed by optical and scanning electron microscopy of the fracture surfaces.The division was clear between strong bonds (GIC of 600- 1000J/m2 and failure in cohesion) and weak bonds (GIC of 80-400J/m2 and failure in adhesion). All prepared laminates showed the imprint of the peel ply texture and evidence of peel ply remnants after fabric removal, either through SEM or XPS. Within an adhesive system, large amounts of SEM-visible peel ply material transfer correlated with poor bond quality and cleaner surfaces with higher bond quality. The both sides of failed weak bonds showed evidence of peel ply remnants under XPS, showing that at least some failure is occurring through the remnants. The choice of adhesive was found to be significant. AF 555 adhesive was more tolerant of peel ply contamination than MB 1515-3. Although the bond quality results varied substantially between tested combinations, the total surface energies of all prepared surfaces were very similar. Single fluid contact angle

  14. Detecting Translation Errors in CAD Surfaces and Preparing Geometries for Mesh Generation

    Energy Technology Data Exchange (ETDEWEB)

    Petersson, N Anders; Chand, K K

    2001-08-27

    The authors have developed tools for the efficient preparation of CAD geometries for mesh generation. Geometries are read from IGES files and then maintained in a boundary-representation consisting of a patchwork of trimmed and untrimmed surfaces. Gross errors in the geometry can be identified and removed automatically while a user interface is provided for manipulating the geometry (such as correcting invalid trimming curves or removing unwanted details). Modifying the geometry by adding or deleting surfaces and/or sectioning it by arbitrary planes (e.g. symmetry planes) is also supported. These tools are used for robust and accurate geometry models for initial mesh generation and will be applied to in situ mesh generation requirements of moving and adaptive grid simulations.

  15. Preparation and surface enhanced Raman scattering behavior of Ag-coated C{sub 60} nanoclusters

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Shi-Zhao; Yin, Die-er; Li, Xiangqing; Mu, Jin, E-mail: mujin@sit.edu.cn

    2013-12-01

    Ag-coated C{sub 60} nanoclusters were prepared and characterized with X-ray diffraction, transmission electron microscopy and nitrogen adsorption–desorption isotherm measurement. The Ag-coated C{sub 60} nanoclusters were assembled on the glass substrate to form a thin film using the layer-by-layer technique. Meanwhile, the surface enhanced Raman scattering (SERS) of musk xylene adsorbed on the film of Ag-coated C{sub 60} nanoclusters was explored. The results indicated that the film of Ag-coated C{sub 60} nanoclusters was a unique SERS-active substrate with a detection limit of 10{sup −9} mol L{sup −1} for musk xylene. Furthermore, the surface enhanced mechanisms were discussed preliminarily.

  16. Preparation and characterization of boron nitride/carbon fiber composite with high specific surface area

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Yan; Fan, Mingwen [Wuhan Univ. (China). Key Laboratory for Oral Biomedical Engineering; Yuan, Songdong; Xiong, Kun; Hu, Kunpeng; Luo, Yi [Hubei Univ. of Technology, Wuhan (China). School of Chemistry and Chemical Engineering; Li, Dong [Hubei Univ. of Technology, Wuhan (China). School of Chemistry and Chemical Engineering; Oxford Univ. (United Kingdom). Chemistry Research Lab.

    2014-06-15

    Boron nitride can be used as a good catalyst carrier because of its high thermal conductivity and chemical stability. However, a high specific surface area of boron nitride is still desirable. In this work, a carbon fiber composite coated with boron nitride villous nano-film was prepared, and was also characterized by means of scanning electron microscopy, high resolution transmission electron microscopy, Fourier transform infrared spectroscopy, and Brunauer-Emmett-Teller analysis. The results indicated that the carbon fibers were covered by uniform villous boron nitride films whose thickness was about 150 - 200 nm. The specific surface area of the boron nitride/carbon fiber composite material was 96 m{sup 2} g{sup -1}, which was markedly improved compared with conventional boron nitride materials. (orig.)

  17. Control of Colloid Surface Chemistry through Matrix Confinement: Facile Preparation of Stable Antibody Functionalized Silver Nanoparticles

    Science.gov (United States)

    Skewis, Lynell R.; Reinhard, Björn M.

    2010-01-01

    Here we describe a simple yet efficient gel matrix assisted preparation method which improves synthetic control over the interface between inorganic nanomaterials and biopolymers and yields stable biofunctionalized silver nanoparticles. Covalent functionalization of the noble metal surface is aided by the confinement of polyethylene glycol acetate functionalized silver nanoparticles in thin slabs of a 1% agarose gel. The gel confined nanoparticles can be transferred between reaction and washing media simply by immersing the gel slab in the solution of interest. The agarose matrix retains nanoparticles but is swiftly penetrated by the antibodies of interest. The antibodies are covalently anchored to the nanoparticles using conventional crosslinking strategies, and the resulting antibody functionalized nanoparticles are recovered from the gel through electroelution. We demonstrate the efficacy of this nanoparticle functionalization approach by labeling specific receptors on cellular surfaces with functionalized silver nanoparticles that are stable under physiological conditions. PMID:20161660

  18. Universal Nature-inspired Coatings for Preparing Non-charging Surfaces.

    Science.gov (United States)

    Fang, Yan; Gonuguntla, Spandhana; Soh, Siowling

    2017-08-18

    Static charge generated by contact electrification on surfaces can lead to many undesirable consequences, such as a reduction in the efficiency of manufacturing processes, damage to equipment, and explosions. However, it is extremely challenging to avoid contact electrification because it is ubiquitous - almost all types of materials charge on contact. Here, we coated materials with naturally-occurring polydopamine (PDA) and tannic acid (TA) for preparing non-charging surfaces. Importantly, these coatings are very versatile and can be coated on a wide range of materials, including metals, inorganic materials, semiconductors, and polymers. Once coated, the amount of charge generated was found to reduce dramatically at different humidities. The reduction in charge may be due to the radical-scavenging property of PDA and TA. This simple general approach is ideal for coating the vast variety of materials that need to resist charging by contact electrification.

  19. [Preparation, characterization and surface-enhanced Raman properties of agarose gel/gold nanoparticles hybrid].

    Science.gov (United States)

    Ma, Xiao-yuan; Liu, Ying; Wang, Zhou-ping

    2014-08-01

    Agarose gel/gold nanoparticles hybrid was prepared by adding gold nanoparticles to preformed agarose gel. Naniocomposite structures and properties were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), and UV-Vis-NIR absorption spectroscopy. Experimental data indicated a uniform distribution of gold nanoparticles adsorbed on agarose gel network And the excellent optical absorption properties were shown. Based on the swelling-contraction characteristics of agarose gel and the adjustable localized surface plasmon resonance (LSPR) of the gold nanoparticles, the nano-composites were used as surface enhanced Raman scattering (SERS) substrate to detect the Raman signal molecules Nile blue A. Results revealed that the porous structure of the agarose gel provided a good carrier for the enrichment of the gold nanoparticles. The gold nanoparticles dynamic hot-spot effect arising from the agarose gel contraction loss of water in the air greatly enhanced the Raman signal.

  20. Preparation of polyamide 6/silica nanocomposites from silica surface initiated ring-opening anionic polymerization

    Directory of Open Access Journals (Sweden)

    2007-07-01

    Full Text Available Polyamide 6/silica nanocomposites were synthesized by in situ ring-opening anionic polymerization of ε-caprolactam in the presence of sodium caprolactamate as a catalyst and caprolactam-functionalized silica as an initiator. The initiator precursor, isocyanate-functionalized silica, was prepared by directly reacting commercial silica with excess toluene 2,4-diisocyanate. This polymerization was found to occur in a highly efficient manner at relatively low reaction temperature (170°C and short reaction times (6 h. FTIR spectroscopy was utilized to follow the introduction and consumption of isocyanate groups on the silica surface. Thermogravimetric analysis indicated that the polyamide 6 was successfully grown from the silica surface. Transmission electron microscopy was utilized to image polymer-functionalized silica, showing fine dispersion of silica particles and their size ranging from 20 to 40 nm.

  1. Influence of surface preparation on atomic layer deposition of Pt films

    Institute of Scientific and Technical Information of China (English)

    Ge Liang; Hu Cheng; Zhu Zhiwei; Zhang Wei; Wu Dongping; Zhang Shili

    2012-01-01

    We report Pt deposition on a Si substrate by means of atomic layer deposition (ALD) using (methylcyclopentadienyl) trimethylplatinum (CH3CsH4Pt(CH3)3) and O2.Silicon substrates with both HF-last and oxidelast surface treatments are employed to investigate the influence of surface preparation on Pt-ALD.A significantlylonger incubation time and less homogeneity are observed for Pt growth on the HF-last substrate compared to the oxide-last substrate.An interfacial oxide layer at the Pt-Si interface is found inevitable even with HF treatment of the Si substrate immediately prior to ALD processing.A plausible explanation to the observed difference of Pt-ALD is discussed.

  2. Preparation of High Surface Area, Large Pore Volume Alumina by Using β-Cyclodextrin as a Non-surfactant Template

    Institute of Scientific and Technical Information of China (English)

    Lai Jun WANG; Ming Fen WEN; Yu Shan LI; Dong YANG; Jing CHEN; Chong Li SONG

    2006-01-01

    A series of alumina samples were prepared using β-cyclodextrin as the non-surfactant template. These samples were characterized by XRD, BET and TEM. The results showed that the alumina samples prepared using β-cyclodextrin template had the higher surface areas (124-484 m2/g), larger pore volumes (0.7-1.27 mL/g) and more thermal stability than samples prepared without using β-cyclodextrin.

  3. Preparation, Study and Modification of Nanometer-Scale Flat TiO2 Surfaces by Electrochemistry and AFM Techniques

    DEFF Research Database (Denmark)

    Dihn Thi, M. T.; Cleemann, Lars Nilausen; Welinder, Anne Christina

    In order to study local properties of surfaces, it is necessary to control their preparation mode to get reproducible and well characterized samples. The first part of this work concerns the preparation of TiO2 films on Ti substrates that fulfil these criteria. The TiO2 formed by anodisation...... to the preparation and the study of TiO2/Ti electrodes “modified” by a Pt-deposit....

  4. Preparation and ion exchange properties of egg-shell glass beads with different surface morphologies

    Institute of Scientific and Technical Information of China (English)

    Chun Shen; Yujun Wang; Jianhong Xu; Yangcheng Lu; Guangsheng Luo

    2012-01-01

    A subcritical water treatment method was developed for preparing porous-surfaced glass beads with an egg-shell structure in a batch reactor.Based on the "corrosion-ion-migration-recondensation" strategy,ordinary soda-lime glass beads with a diameter of about 100 μ(m)ere made first to react with subcritical water to effect controlled quantity of silicate dissolution of glass by adjusting treatment time and temperature.The dissolved silicate was then made to recondense on the glass core to form different porous shell morphologies:pores,flakes and fibers.Among these,glass beads coated with fibers with surface area of 154.5 m2/g,pore volume of 0.27 cm3/g and pore size of 7.1 nm were obtained at 573 K after 2 h of treatment.The prepared porous-surfaced glass beads were then used as adsorbent for heavy metal ions,showing various ion exchange properties.Glass beads covered with fibers displayed fast kinetics and high sorption capacity because of their egg-shell structure and high surface area.More than 90% of copper ions were adsorbed within 100 min from a solution with an initial concentration of 110 mg/L at 313 K.Ion sorption capacities were 149.33,81.33 and 42.96 mg/g respectively for Ag+,Cu2+ and Ni2+ at 313 K.A green and low-cost method was thus developed to produce egg-shell-structured porous glass with high sorption capacity.

  5. Preparation, Study and Modification of Nanometer-Scale Flat TiO2 Surfaces by Electrochemistry and AFM Techniques

    DEFF Research Database (Denmark)

    Dihn Thi, M. T.; Cleemann, Lars Nilausen; Welinder, Anne Christina

    In order to study local properties of surfaces, it is necessary to control their preparation mode to get reproducible and well characterized samples. The first part of this work concerns the preparation of TiO2 films on Ti substrates that fulfil these criteria. The TiO2 formed by anodisation of t...

  6. High pressure CO hydrogenation over bimetallic Pt-Co catalysts

    DEFF Research Database (Denmark)

    Christensen, Jakob Munkholt; Medford, Andrew James; Studt, Felix

    2014-01-01

    The potential of bimetallic Pt-Co catalysts for production of higher alcohols in high pressure CO hydrogenation has been assessed. Two catalysts (Pt3Co/SiO2 and PtCo/SiO2) were tested, and the existing literature on CO hydrogenation over Pt-Co catalysts was reviewed. It is found that the catalyst...

  7. Surface-Enhanced Raman Scattering Study of Silver Nanoparticles Prepared by Using MC as a Template

    Directory of Open Access Journals (Sweden)

    Yudong Lu

    2013-01-01

    Full Text Available A good Ag-based SERS substrate has been prepared by one-pot reaction using methyl cellulose as a template. Effects of methyl cellulose concentration, silver ammonia chloride solution concentration, reaction duration, and reducing agent on silver nanoparticles were discussed in this paper. The performance of the obtained Ag nanoparticles was characterized by UV-visible spectroscopy, transmission electron microscopy, and surface-enhanced Raman spectroscopy. Results show that the reducing agent plays a crucial role in the performance of silver nanoparticles. Optimum preparation conditions of synthesis of SERS substrates were as follows: 10 mM silver ammonia chloride and 0.2% MC at 75°C, reducing in 0.2% reducing agent at 120 min. TEM studies reveal that particles are mostly spherical and rod in shape with an average size of 80 nm. Silver nanoparticles prepared with MC as a template have been shown to provide strong SERS enhancement signals of R6G, which can be used as a good Ag-based SERS substrate in the analytical environment for routine measurements.

  8. First principles investigations of small bimetallic PdGa clusters as catalysts for hydrogen dissociation

    Science.gov (United States)

    Kaul, Indu; Ghosh, Prasenjit

    2017-04-01

    Using first principles density functional theory based calculations, we have studied hydrogen dissociation on sub nanometer bimetallic clusters formed from d-block (Pd) and p-block (Ga) elements in gas phase to explore the feasibility of using them as cheap catalysts for hydrogen dissociation. Our calculations show that the dimers, trimers and tetramers of these clusters are thermodynamically more stable than the pure ones for all Ga concentrations. For a given cluster size, we find that the clusters containing equal amount of Pd and Ga are the most stable ones. In contrast to bulk PdGa, the contribution of Pd-d states to the highest occupied molecular orbitals of the bimetallic clusters are either very small or absent. Study of adsorption of hydrogen molecule on these clusters show that hydrogen binds in an activated form only on the Pd rich clusters. From the calculations of hydrogen dissociation barriers on tetramers of pure Pd, 25% Ga (Pd3Ga) and 50% Ga (Pd2Ga2) we find that Pd3Ga is the most efficient catalyst for hydrogen dissociation with barriers even lower than that on the PdGa surfaces.

  9. Photochemical synthesis of mono and bimetallic nanoparticles and their use in catalysis

    Science.gov (United States)

    Pardoe, Andrea

    2011-07-01

    Nanomaterials have become a popular topic of research over the years because of their many important applications. It can be a challenge to stabilize the particles at a nanometer size, while having control over their surface features. Copper nanoparticles were synthesized photochemically using a photogenerated radical allowing spatial and temporal control over their formation. The synthesis was affected by the stabilizers used, which changed the size, dispersity, rate of formation, and oxidation rate. Copper nanoparticles suffer from their fast oxidation in air, so copper-silver bimetallic nanoparticles were synthesized in attempts to overcome the oxidation of copper nanoparticles. Bimetallic nanoparticles were synthesized, but preventing the oxidation of the copper nanoparticles proved difficult. One important application of nanoparticles that was explored here is in catalyzing organic reactions. Because of the fast oxidation of copper nanoparticles, silver nanoparticles were synthesized photochemically on different supports including TiO2 and hydrotalcite (HTC). Their catalytic efficiency was tested using alcohol oxidations. Different silver nanoparticle shapes (decahedra and plates) were compared with the spheres to see the different catalytic efficiencies.

  10. Oxidizing capacity of periodate activated with iron-based bimetallic nanoparticles.

    Science.gov (United States)

    Lee, Hongshin; Yoo, Ha-Young; Choi, Jihyun; Nam, In-Hyun; Lee, Sanghyup; Lee, Seunghak; Kim, Jae-Hong; Lee, Changha; Lee, Jaesang

    2014-07-15

    Nanosized zerovalent iron (nFe0) loaded with a secondary metal such as Ni or Cu on its surface was demonstrated to effectively activate periodate (IO4-) and degrade selected organic compounds at neutral pH. The degradation was accompanied by a stoichiometric conversion of IO4- to iodate (IO3-). nFe0 without bimetallic loading led to similar IO4- reduction but no organic degradation, suggesting the production of reactive iodine intermediate only when IO4- is activated by bimetallic nFe0 (e.g., nFe0-Ni and nFe0-Cu). The organic degradation kinetics in the nFe0-Ni(or Cu)/IO4- system was substrate dependent: 4-chlorophenol, phenol, and bisphenol A were effectively degraded, whereas little or no degradation was observed with benzoic acid, carbamazepine, and 2,4,6-trichlorophenol. The substrate specificity, further confirmed by little kinetic inhibition with background organic matter, implies the selective nature of oxidant in the nFe0-Ni(or Cu)/IO4- system. The comparison with the photoactivated IO4- system, in which iodyl radical (IO3•) is a predominant oxidant in the presence of methanol, suggests IO3• also as primary oxidant in the nFe0-Ni(or Cu)/IO4- system.

  11. Active site of bimetallic heterogeneous catalyst by atomic resolution aberration-corrected STEM

    Energy Technology Data Exchange (ETDEWEB)

    Hsiao, Chien-Nan, E-mail: 0209347@narlabs.org.tw; Lin, Chun-Ting

    2015-11-01

    Highlights: • Up to fifth order aberration coefficients of STEM had been compensated. • The core-shell structural catalyst was identified by Z-contrast image. • Atomic twinning in nanoparticle was revealed by aberration-corrected STEM. - Abstract: The localized defect of Au–Pd bimetallic heterogeneous nanoparticles catalyst was investigated using HRTEM and aberration-corrected HRSTEM. The phase plates were calculated from the aberration coefficients of the measured probe tableau for various outer tilt angle of the optical axis and the accuracy required for the compensation of the various residual aberration coefficients in order to achieve sub-angstrom resolution with the electron optics system was evaluated up to the fifth order aberrations. It is found that the interplanar spacing of the Au–Pd nanoparticle (1 1 1) planes observed along the [1 1 0] zone axis was approximately 0.24 nm measured by HRTEM. In addition, the HRSTEM HAADF image demonstrated that the twin boundaries on the surfaces of heterogeneous nanoparticles catalysts at atomic scale. These defects might be introduced during the growth to alleviate the internal stress caused by the 4.6% lattice mismatch of Au–Pd bimetallic system. Current research could be applied to the study of active sites in nanocatalysts.

  12. Influence of surface preparation on fracture load of resin composite-based repairs

    Science.gov (United States)

    Mateos-Palacios, Rocío; Román-Rodríguez, Juan-Luis; Solá-Ruíz, María-Fernanda; Fons-Font, Antonio

    2015-01-01

    The purpose of the present study is to evaluate the fracture load of composite-based repairs to fractured zirconium oxide (Z) crowns and to ceramic-fused-to-metal (CM) crowns, comparing different mechanical surface preparation methods. A total of 75 crowns were repaired; samples then underwent dynamic loading and thermocycling. Final fracture load values for failure of the repaired crowns were measured and the type of fracture registered. Group I: CM: Surface preparation with a diamond bur + 9.5% Hydrofluoric Acid (HF) etching; Group II): CM: air-particle (Al2O3) + 9.5% HF; Group III: CM: Silica coating (SiO2); Group IV): Z: air-particle (Al2O3) + HF 9.5%; Group V) Z: Silica coating (SiO2). Of the three CM groups, Group I (CM-diamond bur) showed the highest mean failure value, with significant difference in comparison with Group III (CM-silica coating). For the zirconia groups, the highest value was obtained by Group V (silica coating). Key words:Crown, ceramic-fused-to-metal, zirconia, resin-composite, ceramic covering. PMID:25810848

  13. Study of Influencing Factors and the Mechanism of Preparing Triazinedithiol Polymeric Nanofilms on Aluminum Surfaces

    Directory of Open Access Journals (Sweden)

    Yanni Li

    2010-11-01

    Full Text Available Triazinedithiol polymeric nanofilm was prepared on a pure aluminum surface by electrochemical polymerization of AF17N. The mechanism of the process was proposed and electrochemical polymerization parameters were investigated. The triazinedithiol polymeric nanofilm had notable lubricity, high dielectric property and superhydrophobic property due to the allyl and fluoro alkyl groups in the AF17N monomer. The chemical structure of poly (6-(N-allyl-1,1,2,2-tetrahydroperfluorodecylamino-1,3,5-triazine-2,4-dithiol monosodium nanofilm (PAF17 was investigated by analysis of FT-IR spectra and X-ray photoelectron spectroscopy (XPS. The optimal conditions for the preparation process were based on the data of film weight and thickness. The optimal parameters of monomer concentration, electropolymerization time and temperature were 5 mM, 6 min and 15 °C, respectively. The electropolymerization mechanism was a radical polymerization reaction. It is expected that this technique will be applied in industrial fields for aluminum and aluminum alloy to achieve functional surfaces.

  14. Influence of surface preparation on fracture load of resin composite-based repairs.

    Science.gov (United States)

    Agustín-Panadero, Rubén; Mateos-Palacios, Rocío; Román-Rodríguez, Juan-Luis; Solá-Ruíz, María-Fernanda; Fons-Font, Antonio

    2015-02-01

    The purpose of the present study is to evaluate the fracture load of composite-based repairs to fractured zirconium oxide (Z) crowns and to ceramic-fused-to-metal (CM) crowns, comparing different mechanical surface preparation methods. A total of 75 crowns were repaired; samples then underwent dynamic loading and thermocycling. Final fracture load values for failure of the repaired crowns were measured and the type of fracture registered. Group I: CM: Surface preparation with a diamond bur + 9.5% Hydrofluoric Acid (HF) etching; Group II): CM: air-particle (Al2O3) + 9.5% HF; Group III: CM: Silica coating (SiO2); Group IV): Z: air-particle (Al2O3) + HF 9.5%; Group V) Z: Silica coating (SiO2). Of the three CM groups, Group I (CM-diamond bur) showed the highest mean failure value, with significant difference in comparison with Group III (CM-silica coating). For the zirconia groups, the highest value was obtained by Group V (silica coating). Key words:Crown, ceramic-fused-to-metal, zirconia, resin-composite, ceramic covering.

  15. Mass Spectrometry as a Preparative Tool for the Surface Science of Large Molecules

    Science.gov (United States)

    Rauschenbach, Stephan; Ternes, Markus; Harnau, Ludger; Kern, Klaus

    2016-06-01

    Measuring and understanding the complexity that arises when nanostructures interact with their environment are one of the major current challenges of nanoscale science and technology. High-resolution microscopy methods such as scanning probe microscopy have the capacity to investigate nanoscale systems with ultimate precision, for which, however, atomic scale precise preparation methods of surface science are a necessity. Preparative mass spectrometry (pMS), defined as the controlled deposition of m/z filtered ion beams, with soft ionization sources links the world of large, biological molecules and surface science, enabling atomic scale chemical control of molecular deposition in ultrahigh vacuum (UHV). Here we explore the application of high-resolution scanning probe microscopy and spectroscopy to the characterization of structure and properties of large molecules. We introduce the fundamental principles of the combined experiments electrospray ion beam deposition and scanning tunneling microscopy. Examples for the deposition and investigation of single particles, for layer and film growth, and for the investigation of electronic properties of individual nonvolatile molecules show that state-of-the-art pMS technology provides a platform analog to thermal evaporation in conventional molecular beam epitaxy. Additionally, it offers additional, unique features due to the use of charged polyatomic particles. This new field is an enormous sandbox for novel molecular materials research and demands the development of advanced molecular ion beam technology.

  16. Preparative soft and reactive landing of gas-phase ions on plasma-treated metal surfaces.

    Science.gov (United States)

    Volný, Michael; Elam, W Timothy; Ratner, Buddy D; Turecek, Frantisek

    2005-08-01

    Soft landing of singly charged gas-phase ions on dry metal surfaces that were pretreated in situ by oxygen plasma results in 0.1-2% total yields of recovered intact compounds. Lysine, peptides, crystal violet dye, and a biotin conjugate are found to survive soft landing of hyperthermal ions of up to 50-eV kinetic energy. Soft landing at 40-50-eV ion kinetic energies of a fluorescence-labeled biotin conjugate results in an immobilized fraction that cannot be washed from the surface and is found to contain an intact biotin moiety. The present results represent an approximately 10(4) fold improvement in soft-landing efficiency and indicate that plasma-treated metal surfaces can be useful for preparative separation of organic and biological molecules by mass spectrometry. The substantial improvement in soft-landing yields results from a high transmission of electrosprayed ions into the vacuum system, efficient and nondestructive discharge of ions on the metal oxide surface, and facile analyte recovery in the absence of a matrix.

  17. Preparation of self-cleaning surfaces with a dual functionality of superhydrophobicity and photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Park, Eun Ji; Yoon, Hye Soo; Kim, Dae Han [Department of Chemistry, Sungkyunkwan University, Suwon, 440-746 (Korea, Republic of); Kim, Yong Ho, E-mail: yhkim94@skku.edu [Department of Chemistry, Sungkyunkwan University, Suwon, 440-746 (Korea, Republic of); SKKU Advanced Institute of Nanotechnology (SAINT), Sungkyunkwan University, Suwon 440-746 (Korea, Republic of); Kim, Young Dok, E-mail: ydkim91@skku.edu [Department of Chemistry, Sungkyunkwan University, Suwon, 440-746 (Korea, Republic of); Biorefinery Research Group, Korean Research Institute of Chemical Technology, Daejeon, 306-600 (Korea, Republic of)

    2014-11-15

    Graphical abstract: - Highlights: • Hydrophobic thin film of polydimethylsiloxane was deposited on SiO{sub 2}. • PDMS-coated SiO{sub 2} and TiO{sub 2} photocatalysts were mixed with various ratios. • Both stable superhydrophobicity and photocatalytic activity appeared on a surface. - Abstract: Thin film of polydimethylsiloxane (PDMS) was deposited on SiO{sub 2} nanoparticles by chemical vapor deposition, and SiO{sub 2} became completely hydrophobic after PDMS coating. Mixtures of TiO{sub 2} and PDMS-coated SiO{sub 2} nanoparticles with various relative ratios were prepared, and distributed on glass surfaces, and water contact angles and photocatalytic activities of these surfaces were studied. Samples consisting of TiO{sub 2} and PDMS-coated SiO{sub 2} with a ratio of 7:3 showed a highly stable superhydrophobicity under UV irradiation with a water contact angle of 165° and UV-driven photocatalytic activity for decomposition of methylene blue and phenol in aqueous solution. Our process can be exploited for fabricating self-cleaning surfaces with dual functionality of superhydrophobicity and photocatalytic activity at the same time.

  18. The preparation of polypyrrole surfaces in the presence of mesoporous silica nanoparticles and their biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Youngnam; Borgens, Richard Ben, E-mail: cho22@purdue.edu [Center for Paralysis Research, School of Veterinary Medicine, Purdue University, West Lafayette, IN 47907 (United States)

    2010-05-21

    The deposition of carboxylic acid-terminated conducting polymer into two- or three-dimensional structures made up of colloidal particles has been successfully completed. This was accomplished using electrochemical deposition of ordered arrays of mesoporous silica nanoparticles (MSNs) as a template. Subsequent removal of the template yielded a porous polypyrrole surface. The co-polymerization of pyrrole with carboxylic acid-terminated pyrrole derivatives overcame the limitations of a lack of reactive functional groups-by facilitating the direct coupling of the film with biomolecules or drugs on the surface. Such Ppy films were characterized by several techniques: (1) scanning electron microscope (SEM) to evaluate surface topography, (2) x-ray photoelectron spectroscopy (XPS) to assess the chemical composition of the films, (3) four-point probe to measure the conductivity, and cyclic voltammogram to observe surface electroactivity. To assay the biological effectiveness of this preparation, we used phase-contrast light microscopy to compare neurite outgrowth from PC 12 cells grown on Ppy films in the presence and absence of electrical stimulation. These electrically functional, biocompatible composites show promise as novel neural implants that would deliver specific biologically active molecules in a highly localized manner to damaged or otherwise vulnerable cells such as found in the nervous system.

  19. Comparison of two tooth-saving preparation techniques for one-surface cavities.

    Science.gov (United States)

    Rahimtoola, Salim; van Amerongen, Evert

    2002-01-01

    The atraumatic restorative treatment technique (ART) is based on removing infected tooth material using only hand instruments and filling the subsequently cleaned cavity with adhesive material such as glass ionomer. As its name suggests, the ART technique should be atraumatic during treatment, as well as for the tooth itself as for the patient. It was primarily developed for treating people living in underserved areas of the world where resources and facilities such as electricity and trained manpower are limited. Many studies have evaluated the ART technique and the results have supported its application. However, a very limited number of studies have compared ART with more conventional techniques. For that reason, a study was conducted in Pakistan, to compare the ART technique with another more conventional treatment technique. The results of this study show that the preparations with hand instruments resulted in smaller sized cavities and therefore may be less traumatic to the tooth. It was also associated with less pain reactions compared to the more conventional technique. Although preparations with hand instruments required more time, this did not seem to affect the survival of restorations. The survival of glass ionomer cement restorations made with hand instruments was comparable with single surface amalgam restorations made with a more conventional technique. Recurrent caries was not associated with any glass ionomer cement restorations made with hand instruments. The retention rate of glass ionomer sealants was low, however one dentist had a sealant retention rate of 81.5 percent that suggests that this procedure can be performed satisfactorily in conjunction with a glass ionomer cement restoration. Operator variances did seem to affect the restorations. Survival of glass ionomer restorations made with both hand and rotary instruments varied for different operators. Similarly, the retention of fissure sealant also varied amongst operators. Operator

  20. The situ preparation of silica nanoparticles on the surface of functionalized graphene nanoplatelets

    Science.gov (United States)

    Li, Jiani; Yu, Kejing; Qian, Kun; Cao, Haijian; Lu, Xuefeng; Sun, Jie

    2014-04-01

    A method for situ preparing a hybrid material consisting of silica nanoparticles (SiO2) attached onto the surface of functionalized graphene nanoplatelets (f-GNPs) is proposed. Firstly, polyacrylic acid (PAA) was grafted to the surface of f-GNPs to increase reacting sites, and then 3-aminopropyltriethoxysilane (APTES) KH550 reacted with abovementioned product PAA-GNPs to obtain siloxane-GNPs, thus providing reaction sites for the growth of SiO2 on the surface of GNPs. Finally, the SiO2/graphene nanoplatelets (SiO2/GNPs) hybrid material is obtained through introducing siloxane-GNPs into a solution of tetraethyl orthosilicate, ammonia and ethanol for hours' reaction. The results from Fourier transform infrared spectroscopy (FTIR) showed that SiO2 particles have situ grown on the surface of GNPs through chemical bonds as Si-O-Si. And the nanostructure of hybrid materials was characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). All the images indicated that SiO2 particles with similar sizes were grafted on the surface of graphene nanoplatelets successfully. And TEM images also showed the whole growth process of SiO2 particles on the surface of graphene as time grows. Moreover, TGA traces suggested the SiO2/GNPs hybrid material had stable thermal stability. And at 900°C, the residual weight fraction of polymer on siloxane-GNPs was about 94.2% and that of SiO2 particles on hybrid materials was about 75.0%. However, the result of Raman spectroscopy showed that carbon atoms of graphene nanoplatelets became much more disordered, due to the destroyed carbon domains during the process of chemical drafting. Through orthogonal experiments, hybrid materials with various sizes of SiO2 particles were prepared, thus achieving the particle sizes controllable. And the factors' level of significance is as follows: the quantity of ammonia > the quantity of tetraethyl orthosilicate (TEOS) > the reaction time.

  1. Preparation of La-Ti Composite Oxide Nanocrystal and Examination of Their Surface Topography with Atomic Force Microscope

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    With sol-gel method, nanometer La-Ti composite oxide was successfully prepared at a low temperature (750~800℃) using polyethylene glycol as dispersant. By means of atomic force microscope, the surface pattern, particle size distribution, and specific surface area were studied. The compound particle surface appears as a smooth sheet, the mean size of the compound is 25.38 nm. On the specific surface, the particle erects at a height of 4.69 nm. The surface area is 58.90 nm2. The La-Ti composite oxide nanocrystal prefers to narrow and even particle size distribution and the homogeneity of surface topography.

  2. Hollow Au/Ag nanostars displaying broad plasmonic resonance and high surface-enhanced Raman sensitivity

    Science.gov (United States)

    Garcia-Leis, Adianez; Torreggiani, Armida; Garcia-Ramos, Jose Vicente; Sanchez-Cortes, Santiago

    2015-08-01

    Bimetallic Au/Ag hollow nanostar (HNS) nanoparticles with different morphologies were prepared in this work. These nanoplatforms were obtained by changing the experimental conditions (concentration of silver and chemical reductors, hydroxylamine and citrate) and by using Ag nanostars as template nanoparticles (NPs) through galvanic replacement. The goal of this research was to create bimetallic Au/Ag star-shaped nanoparticles with advanced properties displaying a broader plasmonic resonance, a cleaner exposed surface, and a high concentration of electromagnetic hot spots on the surface provided by the special morphology of nanostars. The size, shape, and composition of Ag as well as their optical properties were studied by extinction spectroscopy, hyperspectral dark field microscopy, transmission and scanning electron microscopy (TEM and SEM), and energy dispersive X-ray spectroscopy (EDX). Finally, the surface-enhanced Raman scattering (SERS) activity of these HNS was investigated by using thioflavin T, a biomarker of the β-amyloid fibril formation, responsible for Alzheimer's disease. Lucigenin, a molecule displaying different SERS activities on Au and Ag, was also used to explore the presence of these metals on the NP surface. Thus, a relationship between the morphology, plasmon resonance and SERS activity of these new NPs was made.Bimetallic Au/Ag hollow nanostar (HNS) nanoparticles with different morphologies were prepared in this work. These nanoplatforms were obtained by changing the experimental conditions (concentration of silver and chemical reductors, hydroxylamine and citrate) and by using Ag nanostars as template nanoparticles (NPs) through galvanic replacement. The goal of this research was to create bimetallic Au/Ag star-shaped nanoparticles with advanced properties displaying a broader plasmonic resonance, a cleaner exposed surface, and a high concentration of electromagnetic hot spots on the surface provided by the special morphology of nanostars

  3. Further Investigation Into the Use of Laser Surface Preparation of Ti-6Al-4V Alloy for Adhesive Bonding

    Science.gov (United States)

    Palmieri, Frank L.; Crow, Allison; Zetterberg, Anna; Hopkins, John; Wohl, Christopher J.; Connell, John W.; Belcher, Tony; Blohowiak, Kay Y.

    2014-01-01

    Adhesive bonding offers many advantages over mechanical fastening, but requires robust materials and processing methodologies before it can be incorporated in primary structures for aerospace applications. Surface preparation is widely recognized as one of the key steps to producing robust and predictable bonds. This report documents an ongoing investigation of a surface preparation technique based on Nd:YAG laser ablation as a replacement for the chemical etch and/or abrasive processes currently applied to Ti-6Al-4V alloys. Laser ablation imparts both topographical and chemical changes to a surface that can lead to increased bond durability. A laser based process provides an alternative to chemical-immersion, manual abrasion, and grit blast process steps which are expensive, hazardous, environmentally unfriendly, and less precise. In addition, laser ablation is amenable to process automation, which can improve reproducibility to meet quality standards for surface preparation. An update on work involving adhesive property testing, surface characterization, surface stability, and the effect of laser surface treatment on fatigue behavior is presented. Based on the tests conducted, laser surface treatment is a viable replacement for the immersion chemical surface treatment processes. Testing also showed that the fatigue behavior of the Ti-6Al-4V alloy is comparable for surfaces treated with either laser ablation or chemical surface treatment.

  4. Probing hydrodesulfurization over bimetallic phosphides using monodisperse Ni2-xMxP nanoparticles encapsulated in mesoporous silica

    Science.gov (United States)

    Danforth, Samuel J.; Liyanage, D. Ruchira; Hitihami-Mudiyanselage, Asha; Ilic, Boris; Brock, Stephanie L.; Bussell, Mark E.

    2016-06-01

    Metal phosphide nanoparticles encapsulated in mesoporous silica provide a well-defined system for probing the fundamental chemistry of the hydrodesulfurization (HDS) reaction over this new class of hydrotreating catalysts. To investigate composition effects in bimetallic phosphides, the HDS of dibenzothiophene (DBT) was carried out over a series of Ni-rich Ni2-xMxP@mSiO2 (M = Co, Fe) nanocatalysts (x ≤ 0.50). The Ni2-xMxP nanoparticles (average diameters: 11-13 nm) were prepared by solution-phase arrested precipitation and encapsulated in mesoporous silica, characterized by a range of techniques (XRD, TEM, IR spectroscopy, BET surface area, CO chemisorption) and tested for DBT HDS activity and selectivity. The highest activity was observed for a Ni1.92Co0.08P@mSiO2 nanocatalyst, but the overall trend was a decrease in HDS activity with increasing Co or Fe content. In contrast, the highest turnover frequency (TOF) was observed for the most Co- and Fe-rich compositions based on sites titrated by CO chemisorption. IR spectral studies of adsorbed CO on the Ni2-xMxP@mSiO2 catalysts indicate that an increase in electron density occurs on Ni sites as the Co or Fe content is increased, which may be responsible for the increased TOFs of the catalytic sites. The Ni2-xMxP@mSiO2 nanocatalysts exhibit a strong preference for the direct desulfurization pathway (DDS) for DBT HDS that changes only slightly with increasing Co or Fe content.

  5. Enhancement of Degradation and Dechlorination of Trichloroethylene via Supporting Palladium/Iron Bimetallic Nanoparticles onto Mesoporous Silica

    Directory of Open Access Journals (Sweden)

    Jianjun Wei

    2016-07-01

    Full Text Available This study is aimed to prevent the agglomeration of Pd/Fe bimetallic nanoparticles and thus improve the efficiency toward degradation and dechlorination of chlorinated organic contaminants. A mesoporous silica with a primary pore diameter of 8.3 nm and a specific surface area of 688 m2/g was prepared and used as the host of Pd/Fe nanoparticles. The Pd/Fe nanoparticles were deposited onto or into the mesoporous silica by reduction of ferrous ion and hexachloropalladate ion in aqueous phase. Batch degradation and dechlorination reactions of trichloroethylene were conducted with initial trichloroethylene concentration of 23.7 mg/L, iron loading of 203 or 1.91 × 103 mg/L and silica loading of 8.10 g/L at 25 °C. Concentration of trichloroethylene occurs on the supported Pd/Fe nanoparticles, with trichloroethylene degrading to 56% and 59% in 30 min on the supported Pd/Fe nanoparticles with weight percentage of palladium to iron at 0.075% and 0.10% respectively. The supported Pd/Fe nanoparticles exhibit better dechlorination activity. When the supported Pd/Fe nanoparticles with a weight percentage of palladium to iron of 0.10% were loaded much less than the bare counterpart, the yield of ethylene plus ethane in 10 h on them was comparable, i.e., 19% vs. 21%. This study offers a future approach to efficiently combine the reactivity of supported Pd/Fe nanoparticles and the adsorption ability of mesoporous silica.

  6. Improved Cellulose Adsorption Method for the Preparation of Perovskite Oxides with Large Specific Surface Area at Low Temperature

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Perovskite-type La1-xSrxMO3-d (x=0,0.1,0.2, B=Co,Fe,Mn) oxides were prepared by pyrolysis of metal salt-(organic acid)-cellulose compound precursors. Low calcination temperatures, usually lower than 600oC, were needed. The specific surface area of the as-prepared oxides is higher than that prepared by the cellulose adsorption method, and is comparable to that prepared by sol-gel method. The effective organic acid could be EDTA acid, citric acid or DL-hydroxysuccinic acid, among them, EDTA acid is the best one.

  7. High-performance PdRu bimetallic catalyst supported on mesoporous silica nanoparticles for phenol hydrogenation

    Science.gov (United States)

    Huang, Chao; Yang, Xu; Yang, Hui; Huang, Peiyan; Song, Huiyu; Liao, Shijun

    2014-10-01

    A high-performance PdRu bimetallic catalyst supported on mesoporous silica nanoparticles (MSN), PdRu/MSN, was prepared by a facile impregnation-hydrogen reduction method. It was found that PdRu/MSN showed 5 times higher activity than that of Pd/MSN towards the liquid-phase hydrogenation of phenol. The catalysts were characterized comprehensively by multiple techniques, X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and hydrogen temperature program reduction (TPR). It was revealed that adding Ru could effectively improve the Pd dispersion and promote the electronic interaction between the Pd and Ru, both of which contribute to enhancing the catalytic activity.

  8. SULFUR-RESISTANT BIMETALLIC NOBLE METAL CATALYSTS FOR AROMATIC HYDROGENATION OF DIESEL FUEL

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Y zeolite supporting noble metal catalysts, as the important industrial catalysts for aromatics hydrogenation, have received increasing attention in recent years. Pd-M/Y bimetallic catalysts, where M is non-noble metal element, were prepared to investigate the effects of the addition of a second metal. Pd-M/Y catalysts were evaluated under the following conditions: H2 pressure 4.2 MPa, MHSV 4.0 h-1, sulfur content in feed 3000 μg/g. The microreactor results indicated that the second metal remarkably affects the hydrogenation activity of Pd/Y catalysts. Among them, Cr and W improve the sulfur resistance of Pd/Y, but La, Mn, Mo and Ag make the sulfur resistance worse and the second metals have no evident influence on product selectivity and acidic properties of the catalysts.

  9. Study of carbon-supported bimetallic PtCu nanoparticles by ASAXS

    Science.gov (United States)

    Bulat, N. V.; Avakyan, L. A.; Pryadchenko, V. V.; Srabionyan, V. V.; Belenov, S. V.; Bugaev, L. A.

    2017-05-01

    Bimetallic platinum-copper nanoparticles on carbon support are studied as a perspective electrochemical catalyst by anomalous small-angle X-ray scattering near the Pt absorption L3-edge. The simultaneous fitting of several diffraction patterns measured at different photon energies lead to a satisfactory agreement between experimental and model curves in the assumption of core-shell structure of the particles with Pt-rich shell and Cu-rich core. It is shown that the average size of as prepared nanoparticles is about 6 nm with distribution spread of about ±2 nm and with thickness of Pt-rich shell approximately 1.6 nm. After annealing at 350o C the average size of the particles increased by two times with additional enlargement of the Pt-rich shell thickness.

  10. Gold-platinum bimetallic nanotubes templated from tellurium nanowires as efficient electrocatalysts for methanol oxidation reaction

    Science.gov (United States)

    Lu, Chenchen; Kong, Wei; Zhang, Huying; Song, Bo; Wang, Zhenghua

    2015-11-01

    In this paper, gold-platinum (Au-Pt) bimetallic nanotubes with different Au/Pt ratio are successfully synthesized through a simple wet-chemical reduction route in which tellurium (Te) nanowires serve as both sacrificial template and reducing agent. The hollow nanostructure of Au-Pt nanotubes is formed due to Kirkendall effect. The as-prepared Au-Pt nanotubes can be applied as catalyst for methanol oxidation reaction, and the results indicate that the Au-Pt nanotubes with an Au/Pt ratio of 1:1 show the best electrochemical catalytic performances. Furthermore, the catalytic activity of the Au-Pt nanotubes is also better than Pt nanotubes and commercial Pt/C catalyst.

  11. Surface modification of bioactive glasses and preparation of PDLLA/bioactive glass composite films.

    Science.gov (United States)

    Gao, Yuan; Chang, Jiang

    2009-08-01

    In order to improve the homogeneous dispersion of particles in the polymeric matrix, 45S5, mesoporous 58S, and 58S bioactive glasses were surface modified by esterification reactions with dodecyl alcohol at reflux temperature of 260 degrees C (named as m-45S5, m-mesoporous 58S, and m-58S, respectively). The modified particles showed better hydrophobicity and longer time of suspension in organic matrix. The PDLLA/bioactive glass composite films were fabricated using surface modified bioactive glass particles through solvent casting-evaporation method. Surface morphology, mechanical property, and bioactivity were investigated. The results revealed that the inorganic particle distribution and tensile strength of the composite films with modified bioactive glass particles were significantly improved while great bioactive properties were maintained. Scanning electron microscopy (SEM) observation illustrated that the modified bioactive glass particles were homogeneously dispersed in the PDLLA matrix. The maximum tensile strengths of composite films with modified bioactive glass particles were higher than that of composite films with unmodified bioactive glass particles. The bioactivity of the composite films were evaluated by being soaked in the simulated body fluid (SBF) and the SEM observation of the films suggested that the modified composite films were still bioactive in that they could induce the formation of HAp on its surface and the distribution of HAp was even more homogeneous on the film. The results mentioned above indicated that the surface modification of bioactive glasses with dodecyl alcohol was an effective method to prepare PDLLA/bioactive glass composites with enhanced properties. By studying the comparisons of modification effects among the three types of bioactive glasses, we could get the conclusion that the size and morphology of the inorganic particles would greatly affect the modification effects and the properties of composites.

  12. Surface wettability of TiO2 nanotube arrays prepared by electrochemical anodization

    Science.gov (United States)

    Liu, Guohua; Du, Kang; Wang, Kaiying

    2016-12-01

    This work reports structural engineering and wettability of titania nanotube arrays (TNTs). The nanotube diameter and thickness of TNT layer increase with increasing of applied voltage from 20 to 40, 60 and 80 V, and the diameter has no relevance to extending anodic duration. The fabricated TNTs are 30-190 nm inner diameter and 5-40 mm height. 10 mL water droplets are applied to define wettability of the TNTs by measuring contact angles. Hydrophilicity is enhanced with increasing diameter of TNTs as well as over-etching occurring on the surface. Large diameter tubes and capillary force provide more space and power for liquid to penetration. The contact angle reduces from 35° to 2° with the tube diameter increasing from 30 to 190 nm. Bare Ti foil is inherently hydrophobic with approximately 90° contact angle. The as-prepared TNTs are hydrophilic with contact angle of 24°, and annealing further improves this property to a contact angle of 13°. The bottom of TNTs shows superhydrophilic due to hydroxide compounds existed on the surface. The metal substrate with tube footprint left presents hydrophobic with contact angle of 68°, which is lower than the bare one. It is believed that wettability on the surface of TNTs is dependent on their morphology and chemical composition.

  13. Preparation and characterization of cationic Pluronic for surface modification and functionalization of polymeric drug delivery nanoparticles

    Directory of Open Access Journals (Sweden)

    G. Gyulai

    2016-03-01

    Full Text Available Biodegradable poly(lactic-co-glycolic acid copolymer, PLGA nanoparticles (NPs with a surface layer of poly (ethylene oxide-poly(propylene oxide-poly(ethylene oxide triblock copolymers, Pluronics, are promising drug carrier systems. With the aim to increase the potential of targeted drug delivery the end group derivative of Pluronics was synthesized in a straightforward way to obtain Pluronic-amines. The formation of functional amine groups was confirmed by fluorescamine method and NMR analysis of their N-(tert-Butoxycarbonyl-L-phenylalanine (Boc-Phe-OH and N-(9-Fluorenylmethoxycarbonyl-L-phenylalanine (Fmoc-Phe-OH conjugates. Pluronic and Pluronic-amine stabilized PLGA NPs prepared by nanoprecipitation were characterized by dynamic light scattering and zeta potential measurements. All of the systems showed high colloidal stability checked by electrolyte induced aggregation, although the presence of Pluronicamine on the surface decreased the zeta potential in some extent. The introduction of reactive primary amine groups into the surface layer of PLGA NPs while preserving the aggregation stability, provides a possibility for coupling of various ligands allowing targeted delivery and also contributes to the improved membrane affinity of NPs.

  14. Preparation of porous polymer monoliths featuring enhanced surface coverage with gold nanoparticles

    KAUST Repository

    Lv, Yongqin

    2012-10-01

    A new approach to the preparation of porous polymer monoliths with enhanced coverage of pore surface with gold nanoparticles has been developed. First, a generic poly(glycidyl methacrylate-co-ethylene dimethacrylate) monolith was reacted with cystamine followed by the cleavage of its disulfide bonds with tris(2-carboxylethyl)phosphine, which liberated the desired thiol groups. Dispersions of gold nanoparticles with sizes varying from 5 to 40. nm were then pumped through the functionalized monoliths. The materials were then analyzed using both energy dispersive X-ray spectroscopy and thermogravimetric analysis. We found that the quantity of attached gold was dependent on the size of nanoparticles, with the maximum attachment of more than 60. wt% being achieved with 40. nm nanoparticles. Scanning electron micrographs of the cross sections of all the monoliths revealed the formation of a non-aggregated, homogenous monolayer of nanoparticles. The surface of the bound gold was functionalized with 1-octanethiol and 1-octadecanethiol, and these monolithic columns were used successfully for the separations of proteins in reversed phase mode. The best separations were obtained using monoliths modified with 15, 20, and 30. nm nanoparticles since these sizes produced the most dense coverage of pore surface with gold. © 2012 Elsevier B.V.

  15. Preparation and Characterization of High Surface Area Activated Carbon Fibers from Lignin

    Directory of Open Access Journals (Sweden)

    Jian Lin

    2016-10-01

    Full Text Available Activated carbon fibers (ACFs were successfully prepared from softwood lignin, which was isolated with polyethylene glycol 400 (PEG-400 as a solvolysis reagent, by water steam activation. The pore characterization and adsorption property of ACFs were investigated. The results showed that all the ACFs with more micropores exhibited high specific surface area and total pore volume which increased with the activation time prolonging; the highest ones were around 3100 m2/g and 1.5 mL/g, respectively. The specific surface area and total pore volume were much larger than those of other types of lignin-based ACFs and activated charcoal. Besides, with increasing activation time, the amount of graphitic carbon, which was the main compound on the surface of ACFs, decreased, while the amount of functional groups containing C–O slightly increased. In addition, the adsorption capacity of ACFs for methylene blue was highly increased as the activation time increased. Accordingly, lignin isolated with PEG is a promising precursor for ACF production.

  16. Anti-bacterial chitosan/zinc phthalocyanine fibers supported metallic and bimetallic nanoparticles for the removal of organic pollutants.

    Science.gov (United States)

    Ali, Fayaz; Khan, Sher Bahadar; Kamal, Tahseen; Anwar, Yasir; Alamry, Khalid A; Asiri, Abdullah M

    2017-10-01

    In this report, we prepared chitosan (CS) membrane, CS/zinc phthalocyanine (ZnPc-CS) composite fibers and pellets as support for the synthesis of zero valent metal nanoparticles. The composite fibers and pellets of ZnPc-CS were prepared by simply dispersing 5wt% of ZnPc in CS solution. ZnPc-CS composite were applied as economical host material for the development of metallic and bimetallic zero valent nanoparticles. The composites of ZnPc-CS were put in 0.1M metals salt solutions (mono- and bi-metallic) for the adsorption of metal ions. The metal ions adsorbed ZnPc-CS fibers were treated with 0.1M sodium borohydride (NaBH4) aqueous solution for conversion of metal ions into nanoparticles.