| 1. |
- Alene Asres, Georgies, et al.
(författare)
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A novel WS2 nanowire-nanoflake hybrid material synthesized from WO3 nanowires in sulfur vapor
- 2016
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Ingår i: Scientific Reports. - : NATURE PUBLISHING GROUP. - 2045-2322. ; 6:25610
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Tidskriftsartikel (refereegranskat)abstract
- In this work, WS2 nanowire-nanoflake hybrids are synthesized by the sulfurization of hydrothermally grown WO3 nanowires. The influence of temperature on the formation of products is optimized to grow WS2 nanowires covered with nanoflakes. Current-voltage and resistance-temperature measurements carried out on random networks of the nanostructures show nonlinear characteristics and negative temperature coefficient of resistance indicating that the hybrids are of semiconducting nature. Bottom gated field effect transistor structures based on random networks of the hybrids show only minor modulation of the channel conductance upon applied gate voltage, which indicates poor electrical transport between the nanowires in the random films. On the other hand, the photo response of channel current holds promise for cost-efficient solution process fabrication of photodetector devices working in the visible spectral range.
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| 2. |
- Halonen, Niina, et al.
(författare)
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Low-temperature growth of multi-walled carbon nanotubes by thermal CVD
- 2011
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Ingår i: Physica status solidi. B, Basic research. - Malden : Wiley-Blackwell. - 0370-1972 .- 1521-3951. ; 248:11, s. 2500-2503
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Tidskriftsartikel (refereegranskat)abstract
- Low-temperature thermal chemical vapor deposition (thermal CVD) synthesis of multi-walled carbon nanotubes (MWCNTs) was studied using a large variety of different precursor compounds. Cyclopentene oxide, tetrahydrofuran, methanol, and xylene: methanol mixture as oxygen containing heteroatomic precursors, while xylene and acetylene as conventional hydrocarbon feedstocks were applied in the experiments. The catalytic activity of Co, Fe, Ni, and their bi-as well as tri-metallic combinations were tested for the reactions. Low-temperature CNT growth occurred at 400 degrees C when using bi-metallic Co-Fe and tri-metallic Ni-Co-Fe catalyst (on alumina) and methanol or acetylene as precursors. In the case of monometallic catalyst nanoparticles, only Co (both on alumina and on silica) was found to be active in the low temperature growth (below 500 degrees C) from oxygenates such as cyclopentene oxide and methanol. The structure and composition of the achieved MWCNTs products were studied by scanning and transmission electron microscopy (SEM and TEM) as well as by Raman and X-ray photoelectron spectroscopy (XPS) and by X-ray diffraction (XRD). The successful MWCNT growth below 500 degrees C is promising from the point of view of integrating MWCNT materials into existing IC fabrication technologies. (C) 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
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| 3. |
- Kordás, Krisztián, et al.
(författare)
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Nanoparticle Dispersions
- 2013
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Ingår i: Springer Handbook of Nanomaterials. - Berlin, Heidelberg : Springer Berlin/Heidelberg. - 9783642205941 - 9783642205958 ; , s. 729-776
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Bokkapitel (refereegranskat)abstract
- This chapter aims to provide an insight into the physics and chemistry of nanoparticle–liquid systems. The first part of the chapter discusses parameters and effects that influence dispersion stability (Sect. 20.1), including particle size and shape as well as the interactions at the interface between the solid and liquid phases. Section 20.2 summarizes the practical aspects of making a dispersion, collecting and listing hundreds of examples from contemporary literature. Because of the broad spectrum of materials in question, the survey is limited to dispersions of inorganic nanoparticles including metals, their oxides/sulfides, some (compound) semiconductors, as well as nanostructured carbon particles such as fullerenes, nanotubes, and graphene/graphite (Sect. 20.3). Dispersions of polymers of either synthetic or biological origin lie beyond the scope of this work. Since a very large fraction of applications are related to various surface coatings using dispersions as the source of nanoparticles, Sect. 20.4 is devoted to drying phenomena and particle self-ordering.
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| 4. |
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| 5. |
- Kumar, Vijay, et al.
(författare)
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Leveraging compressive stresses to attenuate the electrical resistivity of buckypaper
- 2016
-
Ingår i: Carbon. - : Elsevier BV. - 0008-6223 .- 1873-3891. ; 110, s. 62-68
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Tidskriftsartikel (refereegranskat)abstract
- Buckypaper (BP) is a planar film that consists of random network of multiwall carbon nanotubes (MWCNTs) held together by weak van der Waals interactions at tube-tube junctions. Although individual carbon nanotubes (CNTs) possess remarkable electrical properties, the electrical resistance of pristine BP is usually too high for practical applications. However, the electrical resistivity of BP can be attenuated by applying modest compressive stresses. Herein, we report an analytical model for predicting the electrical resistivity of BP under defined level of compressive strain. The predictive piezoresistive model of BP was developed by formulating a direct relationship with the structural parameters, physical and electrical properties of CNTs. The basis of the piezoresistive model relied upon the geometrical probability approach in combination with classical Hertzian contact mechanics and constriction resistance techniques. A comparison has been made between the theoretical and experimental results of electrical resistivity of BPs with varying densities. A reasonably good quantitative agreement was obtained between the theory and experiments. The main source of error was caused by the uncertainty in the measurement of the initial BP thickness. Through theoretical modeling, the initial volume fraction of CNTs was found to be one of the key parameters that modulated the piezoresistive behavior of BP.
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| 6. |
- Mohl, Melinda, et al.
(författare)
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Formation of CuPd and CuPt Bimetallic Nanotubes by Galvanic Replacement Reaction
- 2011
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Ingår i: The Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 115:19, s. 9403-9409
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Tidskriftsartikel (refereegranskat)abstract
- A galvanic replacement reaction has been successfully applied to prepare CuPd and CuPt bimetallic nanotubes. The nanotubes were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM) combined with energy dispersive X-ray spectroscopy (EDS), and X-ray diffraction (XRD) techniques. Ultralong, single crystalline copper nanowires (NWs) with a diameter of similar to 64 nm and a length of several micrometers were used as template material. By controlling the amount of noble metal salt added, nanotubes with different compositions were obtained. After the replacement of Cu with Pt, nanotubes composed of a PtCu alloy were formed. EDS analysis revealed that the Pt content increased until about 66%. No further increase in the molar ratio resulted in any additional Pt incorporation into the alloy. As for the replacement of Cu with Pd, the thickening of the nanotubes was observed indicating that nanotubes composed of Pd nanoparticles were formed. Bacicscattered electron imaging and SEM-EDS revealed CuPd nanotubes with approximately 2.3% Cu content. These remarks indicate different evolution mechanism for the nanotubes in the two systems.
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| 7. |
- Mohl, Melinda, et al.
(författare)
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Titania nanofibers in gypsum composites : an antibacterial and cytotoxicology study
- 2014
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Ingår i: Journal of Material Chemistry B. - : Royal Society of Chemistry. - 2050-750X .- 2050-7518. ; 2:10, s. 1307-1316
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Tidskriftsartikel (refereegranskat)abstract
- Further developments of antibacterial coatings based on photocatalytic nanomaterials could be a promising route towards potential environmentally friendly applications in households, public buildings and health care facilities. Hereby we describe a simple chemical approach to synthesize photocatalytic nanomaterial-embedded coatings using gypsum as a binder. Various types of TiO2 nanofiber-based photocatalytic materials (nitrogen-doped and/or palladium nanoparticle decorated) and their composites with gypsum were characterized by means of scanning (SEM) and transmission (TEM) electron microscopy as well as electron and X-ray diffraction (XRD) and energy-dispersive X-ray spectroscopy (EDX) techniques. These gypsum-based composites can be directly applied as commercially available paints on indoor walls. Herein we report that surfaces coated with photocatalytic composites exhibit excellent antimicrobial properties by killing both methicillin-sensitive Staphylococcus aureus (MSSA) and methicillin-resistant Staphylococcus aureus (MRSA) under blue light. In the case of MSSA cells, the palladium nanoparticle-decorated and nitrogen-doped TiO2 composites demonstrated the highest antimicrobial activity. For the MRSA strain even pure gypsum samples were proven to be efficient in eradicating Gram-positive human pathogens. The cytotoxicity of freestanding TiO2 nanofibers was revealed by analyzing the viability of HeLa cells using MTT and fluorescent cell assays.
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| 8. |
- Mäklin, Jani, et al.
(författare)
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Thermal diffusivity of aligned multi-walled carbon nanotubes measured by the flash method
- 2011
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Ingår i: Physica status solidi. B, Basic research. - : John Wiley & Sons. - 0370-1972 .- 1521-3951. ; 248:11, s. 2508-2511
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Tidskriftsartikel (refereegranskat)abstract
- Thermal diffusivity of freestanding catalytic chemical vapor deposition (CCVD) grown multi-walled carbon nanotube (MWCNT) forests (height of 1.5 and 1.9 mm) was characterized in the temperature range between 25 and 200 degrees C. Copper and Al-alloy metal blocks were used as references for validation of the experimental setup. The measurements were carried out along the MWCNT alignment direction with a thermal property analyzer that uses the flash method. The thermal diffusivities measured at room temperature for as-grown and post-annealed (2 h at 480 degrees C in open air) samples were found to be similar to 0.45 and similar to 0.23 cm(2)/s, respectively. In both cases, the thermal diffusivity values were slightly decreasing with increasing temperature. The observed decrease in diffusivity after annealing is most probably due to the loss of amorphous carbon in the specimens and also because of the increased defect density in the nanotube walls resulting in a more pronounced phonon scattering in the lattice. The measured thermal diffusivities for as-grown samples agree with data reported elsewhere for similar MWCNT materials [W. Yi et al., Rev. B 59, 9015 (1999) and T. Borca-Tasciuc et al., J. Appl. Phys. 98, 054309 (2005)]. (C) 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
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| 9. |
- Rawal, Amit, et al.
(författare)
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Ultrasonic fortification of interfiber autohesive contacts in meltblown nonwoven materials
- 2024
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Ingår i: Journal of Advanced Joining Processes. - 2666-3309. ; 9
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Tidskriftsartikel (refereegranskat)abstract
- Autohesion is a unique class of adhesion that enables the bonding of two identical surfaces by establishing intimate contact at interfaces. Creating intimacy between two identical surfaces poses a challenging task, often constrained by the presence of surface roughness and chemical heterogeneity. To surmount this challenge, we document a variety of autohesive traits in polypropylene-based meltblown nonwovens, accomplished through a facile, scalable, energy-efficient, and cost-effective ultrasonic bonding process. The mean work of autohesion for a single polypropylene bond, serving as a figure of merit, has been computed by extending the classical Johnson−Kendall−Roberts (JKR) theory by factoring in peel strength along with key fiber and structural parameters of nonwoven materials. Achieving a high figure of merit in ultrasonically bonded nonwovens hinges on the synergistic interplay of key process parameters, including static force, power, and welding speed, with the fiber and structural properties acting in concert. In this regard, peel-off force analysis has also been conducted on a series of twenty-seven ultrasonically bonded meltblown nonwovens prepared using a 33 full factorial design by systematically varying process parameters (static force, power, and welding speed) across three levels and extension rate. X-ray microcomputed tomography (microCT) analysis has been performed on select ultrasonically bonded nonwoven samples to discern their bulk characteristics. A broad spectrum of mean work of autohesion for a single polypropylene bond, ranging from 1.88 to 9.93 J/m², has been ascertained by modulating key process parameters.
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| 10. |
- Sharma, Sumit, 1990-, et al.
(författare)
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Droplet navigation on metastable hydrophobic and superhydrophobic nonwoven materials
- 2024
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Ingår i: Colloids and Surfaces A. - 0927-7757 .- 1873-4359. ; 683
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Tidskriftsartikel (refereegranskat)abstract
- Rendering any surface non-wettable requires it to be clean and dry after the droplet is deposited or impacted. Leveraging and quantifying the non-periodic or random topology non-wettable is intricate as the Cassie-Baxter state competes with the Wenzel or impaled state, which becomes further challenging for irregular and heterogeneous nonwoven materials. Herein, we report the fundamental insights of the impalement dynamics of droplets on metastable nonwovens and self-similar nonwoven-titanate nanostructured materials (SS-Ti-NMs) using laser scanning confocal microscopy in three dimensions. Our results represent the first example of liquid imbibition in metastable nonwovens and SS-Ti-NMs involving a complex interplay between a triumvirate of factors – the number of fibres in the defined cross-sectional area (volume), pore features, and intrinsic wetting properties of the constituent entities. Predictive models of the apparent contact angle and breakthrough pressure for nonwovens and their SS-Ti-NMs have been proposed based on micro- and nano-scale structural parameters. Enabled by X-ray microcomputed tomography analysis, a key set of three-dimensional fibre and structural parameters of nonwovens has been unveiled, which played a vital role in validating the predictive models of apparent contact angles.
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| 11. |
- Siddharth, Shukla, et al.
(författare)
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Probing the three-dimensional porous and tortuous nature of absorptive glass mat (AGM) separators
- 2020
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Ingår i: Journal of Energy Storage. - : Elsevier BV. - 2352-152X .- 2352-1538. ; 2017:101003
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Tidskriftsartikel (refereegranskat)abstract
- The valve regulated lead acid (VRLA) battery is a predominant electrochemical storage system that stores energy in a cheap, reliable and recyclable manner for innumerable applications. The absorptive glass mat (AGM) separator is a key component, which is pivotal for the successful functioning of the VRLA battery. Herein, the intricate three-dimensional (3D) porous structure of AGM separators has been unveiled using X-ray micro-computed tomography (microCT) analysis. X-ray microCT has quantified a variety of fiber and structural parameters including fiber orientation, porosity, tortuosity, pore size distribution, pore interconnectivity and pore volume distribution. A predictive model of hydraulic tortuosity has been developed based upon some of these fiber and structural parameters. Moreover, the pore size distribution extracted via X-ray microCT analysis has served as a benchmark for making a comparison with the existing analytical model of the pore size distribution of AGM separators. Pore size distributions obtained via the existing analytical model and through X-ray microCT analysis are in close agreement.
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| 12. |
- Sranko, David, et al.
(författare)
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Synthesis and properties of novel Ba(II)Fe(III) layered double hydroxides
- 2010
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Ingår i: Applied Clay Science. - : Elsevier BV. - 1872-9053 .- 0169-1317. ; 48:1-2, s. 214-217
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Tidskriftsartikel (refereegranskat)abstract
- Double hydroxides of Ba(II) and Fe(III) were prepared by the co-precipitation method. Co-precipitation was facilitated by applying highly alkaline, carbonate free NaOH solutions with varying base concentrations (2-20 M). The substances, thus obtained, were characterised by thermal methods. XRD spectra of samples treated at various temperatures, Mossbauer and X-ray absorption spectroscopies. It was found that in extremely concentrated base solutions (>= 10 M) layered double hydroxides, most probably with intercalated OH ions, were formed, indeed, while at low base concentration the Fe(III) ions were precipitated as various oxyhydroxides and the Ba(II) ions remained dissolved. (C) 2009 Elsevier B.V. All rights reserved.
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| 13. |
- Szabados, Márton, et al.
(författare)
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Effects of ultrasonic irradiation on the synthesis, crystallization, thermal and dissolution behaviour of chloride-intercalated, co-precipitated CaFe-layered double hydroxide
- 2019
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Ingår i: Ultrasonics Sonochemistry. - : Elsevier BV. - 1350-4177. ; 55, s. 165-173
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Tidskriftsartikel (refereegranskat)abstract
- The output power (30–150 W) and the periodicity (20–100%) of ultrasound emission were varied in a wide range to regulate and improve the crystallization process in the commonly used co-precipitation technique of chloride-intercalated CaFe-layered double hydroxides. The influence of ultrasound irradiation on the as-prepared materials was studied by X-ray diffractometry, dynamic light scattering, UV–Vis–NIR diffuse reflectance spectroscopy, specific surface area measurement, pore size analysis, ion-selective electrode potentiometric investigations and thermogravimetry. Additionally, structural alterations due to heat treatment at various temperatures were followed in detail by Fourier-transform infrared and X-ray absorption spectroscopies as well as scanning electron microscopy. The ultrasonic treatment was capable of controlling the sizes of primarily formed (from 19 nm to 30 nm) as well as the aggregated (secondary) particles (between 450 nm and 700 nm), and thus modifying their textural parameters and enhancing the incorporation of chloride anions into the interlamellar space. For the first time, the optical energy gap of CaFe-LDH was reported here depending on the nature of applied stirring (4.18–4.34 eV). The heat-treatment investigations revealed that the layered structure was stabile until 200 °C, even at the atomic level.
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| 14. |
- Szabados, Márton, et al.
(författare)
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Synthesis of high-quality, well-characterized CaAlFe-layered triple hydroxide with the combination of dry-milling and ultrasonic irradiation in aqueous solution at elevated temperature
- 2016
-
Ingår i: Ultrasonics Sonochemistry. - : Elsevier BV. - 1350-4177. ; 32, s. 173-180
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Tidskriftsartikel (refereegranskat)abstract
- The combination of mechanochemical and ultrasonic treatment was applied to synthesize CaAlFe-layered triple hydroxides with carbonate or chloride anions in the interlamellar space. The optimal parameters of the preparation were explored by altering the initial ratio of the metal ions and the temperature of ultrasonic irradiation. The resulting triple hydroxides were characterized by X-ray diffractometry, infrared and X-ray absorption spectroscopies, thermogravimetric analysis and scanning electron microscopy. The products were close-to-phase-pure CaAlFe-layered triple hydroxides. Elevation of the temperature transformed the CaAlFe-Cl--layered triple hydroxide to rare oxyhalides (Ca2FeO3Cl and Ca12Al14O32Cl2).
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| 15. |
- Szabados, Márton, et al.
(författare)
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Ultrasonically-enhanced preparation, characterization of CaFe-layered double hydroxides with various interlayer halide, azide and oxo anions (CO3 2−, NO3 −, ClO4 −)
- 2018
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Ingår i: Ultrasonics Sonochemistry. - : Elsevier BV. - 1350-4177. ; 40, s. 853-860
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Tidskriftsartikel (refereegranskat)abstract
- An ultrasonically-enhanced mechanochemical method was developed to synthesize CaFe-layered double hydroxides (LDHs) with various interlayer anions (CO3 2−, NO3 −, ClO4 −, N3 −, F−, Cl−, Br− and I−). The duration of pre-milling and ultrasonic irradiation and the variation of synthesis temperature in the wet chemical step were investigated to obtain the optimal parameters of preparation. The main method to characterize the products was X-ray diffractometry, but infrared and synchrotron-based X-ray absorption spectroscopies as well as thermogravimetric measurements were also used to learn about fine structural details. The synthesis method afforded successful intercalation of the anions, among others the azide anion, a rarely used counter ion providing a system, which enables safe handling the otherwise highly reactive anion. The X-ray absorption spectroscopic measurements revealed that the quality of the interlayered anions could modulate the spatial arrangement of the calcium ions around the iron(III) ions, but only in the second coordination sphere.
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| 16. |
- Varga, Gábor, et al.
(författare)
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Cu(II)-amino acid–CaAl-layered double hydroxide complexes, recyclable, efficient catalysts in various oxidative transformations
- 2016
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Ingår i: Journal of Molecular Catalysis A: Chemical. - : Elsevier BV. - 1381-1169. ; 423, s. 49-60
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Tidskriftsartikel (refereegranskat)abstract
- Intercalated composite materials were prepared with CaAl-layered double hydroxide as host and Cu(II)-amino acid (L-cysteine, L-histidine and L-tyrosine) complex anions as guests. Two methods (intercalation of the ligand first followed by constructing the complex; preforming the complex first, then introducing it among the layers of the host) and optimization of the synthesis conditions were performed to obtain composites having the complex exclusively among the layers. The composite materials were structurally characterized by powder X-ray diffractometry, mid infrared (IR) spectroscopy with ATR (attenuated total reflectance) or photoacoustic detections, transmission and scanning electron microscopies and X-ray photoelectron spectroscopy. Structural features of the intercalant (coordination number, coordination sites) were elucidated by classical chemical and energy dispersive X-ray analyses, EPR (electron paramagnetic spectroscopy), X-ray absorption and far IR spectroscopies. Structural models based on these methods are also given. Catalytic activities, selectivities and recycling abilities of the substances were studied in the oxidation reactions of cyclohexene with peracetic acid and in situ formed iodosylbenzene as oxidants in the liquid phase. The catalysts were active in the Ullmann coupling reaction as well. The intercalated substances were found to be efficient and highly selective catalysts with very good recycling abilities.
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| 17. |
- Varga, Gábor, et al.
(författare)
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Mn(II)-amino acid complexes intercalated in CaAl-layered double hydroxide - Well-characterized, highly efficient, recyclable oxidation catalysts
- 2016
-
Ingår i: Journal of Catalysis. - : Elsevier BV. - 0021-9517. ; 335, s. 125-134
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Tidskriftsartikel (refereegranskat)abstract
- Intercalated composite materials were prepared with CaAl-layered double hydroxide as the host and Mn(II)-amino acid (l-cysteine, l-histidine and l-tyrosine) complex anions as the guest. Two methods (intercalation of the ligand first followed by constructing the complex; preforming the complex first, then introducing it among the layers of the host) and optimization of the auxiliary conditions were performed to arrive at composites having the complex exclusively among the layers. The obtained substances were structurally characterized by powder X-ray diffractometry, mid IR spectroscopy in diffuse reflectance mode and with ATR or photoacoustic detections, and scanning electron microscopy. The structural features of the intercalant (coordination number, coordination sites) were elucidated by classical chemical and energy dispersive X-ray analyses, EPR, X-ray absorption and far IR spectroscopies. Structural models are also given. The catalytic activities, selectivities and recycling abilities of the substances were studied in the oxidation reactions of cyclohexene with peracetic acid and in situ formed iodosylbenzene as oxidants and allylic alcohol with peracetic acid, in the liquid phase. The intercalated substances proved to be efficient and highly selective (with peracetic acid: outstanding epoxide, with iodosylbenzene superior diol selectivities) catalysts with very good recycling abilities.
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| 18. |
- Varga, Gábor, et al.
(författare)
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Ni-Amino Acid–CaAl-Layered Double Hydroxide Composites : Construction, Characterization and Catalytic Properties in Oxidative Transformations
- 2017
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Ingår i: Topics in Catalysis. - : Springer Science and Business Media LLC. - 1022-5528 .- 1572-9028. ; 60:17-18, s. 1429-1438
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Tidskriftsartikel (refereegranskat)abstract
- Host–guest composite materials were prepared applying the anionic forms of Ni(II)-amino acid (l-histidine, l-cysteine, and l-tyrosine) as the guests and CaAl-layered double hydroxide (CaAl-LDH) as the host. The syntheses were performed either by introducing the amino acid anions first and then constructing the metal ion–amino acid complexes or intercalating the pre-prepared complexes in anionic forms. The pristine as well as the composite LDH samples were structurally characterized by X-ray diffractometry, mid IR spectroscopy and scanning electron microscopy. The structural features of the interlayer complexes were studied by UV–Vis, inductively coupled plasma optical emission, mid and far IR and X-ray absorption spectroscopies as well as energy-dispersed X-ray analysis. On the basis of the acquired data, structural models were constructed. The composites were applied as catalysts in the liquid-phase oxidation of cyclohexene applying peracetic acid and the in situ formed iodosyl benzene as oxidants. Using peracetic acid afforded epoxide, while applying iodosyl benzene provided cis diol as the major or exclusive oxidation product. The catalysts displayed good recycling properties.
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| 19. |
- Varga, Gábor, et al.
(författare)
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Syntheses, characterization and catalytic activities of CaAl-layered double hydroxide intercalated Fe(III)-amino acid complexes
- 2018
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Ingår i: Catalysis Today. - : Elsevier BV. - 0920-5861. ; 306, s. 42-50
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Tidskriftsartikel (refereegranskat)abstract
- Synthesis of intercalated composites were carried out using CaAl-LDH (layered double hydroxide) as host and the anionic form of Fe(III)-amino acid complexes as guest materials. Intercalation was attempted with two methods either introducing the preformed complexes or constructing the complex among the layers of the LDH. After optimization of the synthesis parameters, structural characterization was performed by X-ray diffractometry, scanning electron microscopy as well as mid and far infrared spectroscopies. Quantitative data about the intercalated complexes were collected by chemical analysis and X-ray absorption spectroscopy investigating the near edge region as well as the extended fine structure. Structural models based on characterization measurements are also given. Catalytic activities, selectivities and recycling abilities of the substances were studied in the oxidation reactions of cyclohexene with peracetic acid and . in situ formed iodosylbenzene as oxidants in the liquid phase. The catalysts were active in the Ullmann-type etherification coupling reaction as well. The intercalated substances were found to be efficient and highly selective catalysts with very good recycling abilities.
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| 20. |
- Wu, Ming-Chung, et al.
(författare)
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Nitrogen-doped anatase nanofibers decorated with noble metal nanoparticles for photocatalytic production of hydrogen
- 2011
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Ingår i: ACS NANO. - : American Chemical Society. - 1936-0851 .- 1936-086X. ; 5:6, s. 5025-5030
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Tidskriftsartikel (refereegranskat)abstract
- We report the synthesis of N-doped TiO2 nanofibers and high photocatalytic efficiency in generating hydrogen from ethanol-water mixtures under UV-A and UV-B irradiation. Titanate nanofibers synthesized by hydrothermal method are annealed in air and/or ammonia to achieve N-doped anatase fibers. Depending on the synthesis route, either interstitial N atoms or new N-Ti bonds appear in the lattice resulting in slight lattice expansion as shown by XPS and HR-TEM analyses, respectively. These nanofibers were then used as support for Pd and Pt nanoparticles deposited with wet impregnation followed by calcination and reduction. In the hydrogen generation tests the N-doped samples were clearly outperforming their un-doped counterparts showing remarkable efficiency not only under UV-B but also with UV-A illumination. Applying 100 mg catalyst (N-doped TiO2 nanofiber decorated with Pt nanoparticles) in 1 L water-ethanol mixture the H2 evolution rates were as high as 700 μmol/h (UV-A) and 2250 μmol/h (UV-B) corresponding to photo energy percentages of ~3.6% and ~12.3%, respectively.
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| 21. |
- Wu, Ming-Chung, et al.
(författare)
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Photocatalytic activity of nitrogen-doped TiO2-based nanowires : a photo-assisted Kelvin probe force microscopy study
- 2013
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Ingår i: Journal of nanoparticle research. - : Springer. - 1388-0764 .- 1572-896X. ; 16:1, s. Article Number: UNSP 2143-
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Tidskriftsartikel (refereegranskat)abstract
- In this study, a set of nitrogen-doped TiO2-based nanomaterials demonstrating photocatalytic activity was developed by combining the efforts of lattice doping and metal nanoparticle decoration and tested for photo-degradation of methylene blue dye by applying solar simulator irradiation. The surface potential shifts of these TiO2-based photocatalytic nanomaterials measured by Kelvin probe force microscope have been used to study the degree of electron generation of the photocatalysts after irradiation and were well correlated with the photocatalytic activity. The nitrogen-doped TiO2 nanowires decorated with Pt nanoparticles can induce obvious electron accumulation and result in a large shift of surface potential. The analysis shows a clear correlation between the surface potential shift and the photodegradation activity. Furthermore, a thorough comparative photocatalytic activity study combined with X-ray photoelectron spectroscopy analysis of the materials-doped with nitrogen under various conditions-reveals that the photocatalytic efficiency of the catalysts is maintained even if the lattice doping is leached e.g., by thermal treatments after doping. By monitoring the surface potential shifts of various TiO2-based photocatalysts by photo-assisted Kelvin probe force microscopy, we obtain a useful tool for developing novel materials with high photocatalytic activity.
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| 22. |
- Wu, Ming-Chung, et al.
(författare)
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Synthesis and Photocatalytic Performance of Titanium Dioxide Nanofibers and the Fabrication of Flexible Composite Films from Nanofibers
- 2012
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Ingår i: Journal of Nanoscience and Nanotechnology. - : American Scientific Publishers. - 1533-4880 .- 1533-4899. ; 12:2, s. 1421-1424
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Tidskriftsartikel (refereegranskat)abstract
- Titanium dioxide nanofibers were synthesized and applied in flexible composite films that are easy to handle and recycle after use. The nanofibers were obtained in a multi-step procedure. First, sodium titanate nanofibers were prepared from TiO2 nanoparticles through the alkali hydrothermal method. In the next step, sodium hydrogen titanate nanofibers were made by washing the sodium titanate nanofibers in HCI solution. Finally, the sodium hydrogen titanate nanofibers were transformed to TiO2 anatase nanofibers by calcination in air. The photocatalytic activity of TiO2 anatase nanofibers were evaluated and compared to a TiO2 nanoparticle catalyst by decomposing methyl orange dye in aqueous solutions. The achieved reaction rate constant of TiO2 anatase nanofibers was comparable to that of Degussa P25. Paper-like flexible composite films were prepared by co-filtrating aqueous dispersions of TiO2 catalyst materials and cellulose. The composite films made from the nanofibers exhibit better mechanical integrity than those of the nanoparticle-cellulose composites.
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| 23. |
- Zhang, Zhfei, et al.
(författare)
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Characterization of CNT Enhanced Conductive Adhesives in Terms of Thermal Conductivity
- 2012
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Ingår i: ECS Transactions. - : The Electrochemical Society. - 1938-5862 .- 1938-6737. - 9781607683186 ; 44:1, s. 1011-1017
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Konferensbidrag (refereegranskat)abstract
- CNTs have excellent thermal, electrical and mechanical properties. They can be used in various ways. One researched field of application is CNT-polymer composites which combine common technologies with advanced materials. This paper will focus on the thermal property of CNT-Ag-filled adhesives and compares the new materials with conventional, electrical Ag-filled conductive adhesives. Several analytical methods, FTIR, Raman analysis, SEM and TEM have been carried out to examine the different surface conditions after physicval and chemical modification of CNTs. The thermal conductivities of composites containing different types of CNTs were investigated. The incorporation of CNTs into polymers resulted in enhancement of the thermal conductivity compared to Ag-filler. The increase of thermal conductivity with addition of CNT filler is obvious, especially for the purified CNT. The value of thermal conductivity is about two times higher than the Ag-filled conductive adhesive. However, improvement on thermal conductivity of the surface modified CNT-filled conductive adhesives is not so obvious. Since the thermal conduction in CNT is by phonon transfer, the nanometric size and the huge interface lead to strong phonon-scattering at the interface. Thus, a relatively low interfacial area, weak interfacial adhesion promotes the conduction of phonons and minimizes coupling losses. According to this, the non-treated MWCNTs seem to have the highest potential to improve the thermal conductivity of epoxies.
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