| 1. |
- de Oliveira, Matheus Mendes, et al.
(författare)
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Hybrid Nanofiller-Enhanced Carbon Fiber-Reinforced Polymer Composites (CFRP) for Lightning Strike Protection (LSP)
- 2024
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Ingår i: ACS Omega. - : AMER CHEMICAL SOC. - 2470-1343. ; 9:33, s. 35567-35578
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Tidskriftsartikel (refereegranskat)abstract
- The aviation industry relies on lightweight carbon fiber-reinforced polymers (CFRP) for fuel efficiency, which necessitates lightning strike protection (LSP) and electromagnetic shielding due to their electrical insulating characteristics. Traditional metallic meshes used for LSP are heavy and corrosion-prone, prompting the exploration of alternatives. This research showcases CFRP nanocomposites with enhanced LSP properties through the incorporation of graphene nanoplatelets (GNPs) and carbon nanotubes (CNTs). While the enhanced conductivity in the nanofilled epoxy matrix did not impact the overall conductivity of CFRP panels, a significant damage reduction was observed after simulated lightning strike tests. Similar approaches in the literature have also noted this discrepancy, but no attempts to reconcile it have been made. This work provides a framework to explain the damage reduction mechanism while accounting for the modest conductivity improvements in the nanoreinforced CFRPs. Additionally, a simple, nondestructive method to assess surface resin degradation after a lightning strike test is proposed, based on the fluorescence of diphenyl ketones. The discussion is supported by electrical conductivity measurements, damage pattern evaluation using the proposed UV-illumination method, ATR-FTIR, and scanning electron microscopy analysis pre- and postlightning strike simulation.
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| 2. |
- Selegård, Linnéa, et al.
(författare)
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Step by step rare-earth catalyzed SiOx annealing and simultaneous formation of Europium- silicide by low coverage of Eu doped Gd2O3 nanoparticles
- 2021
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Ingår i: Surface Science. - : Elsevier BV. - 0039-6028 .- 1879-2758. ; 704
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Tidskriftsartikel (refereegranskat)abstract
- We report the formation of silicide by annealing of a SiOx surface, with low coverage of Eu doped Gd2O3 nanoparticles. The annealing temperature required for removal of native oxide from the Si substrate decreases with close to 200 °C in presence of the nanoparticles. X-ray photoemission electron microscopy, low-energy electron microscopy and mirror electron microscopy are used to monitor the silicide formation and SiOx removal. Fragmentation of the nanoparticles is observed, and the SiOx layer is gradually removed. Eu migrates to clean Si areas during the annealing process, while Gd is found in areas where oxide is still present. This annealing process is clearly facilitated in the presence of rare-earth based nanoparticles, where nanoparticles are suggested to function as reaction sites to catalyze the oxygen removal and simultaneously form Eu based silicide. Reduction of the annealing temperature of SiOx substrates is also observed in presence of pure Eu3+ and Gd3+ ions. Simultaneous oxygen removal and EuSi formation enable this new rare-earth catalyzed annealing and silicide formation to find applications both within optoelectronics and processing microelectronic industry.
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| 3. |
- Ahrén, Maria, et al.
(författare)
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A simple polyol-free synthesis route to Gd 2O 3 nanoparticles for MRI applications : An experimental and theoretical study
- 2012
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Ingår i: Journal of nanoparticle research. - : Springer. - 1388-0764 .- 1572-896X. ; 14:8
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Tidskriftsartikel (refereegranskat)abstract
- Chelated gadolinium ions, e.g., Gd-DTPA, are today used clinically as contrast agents for magnetic resonance imaging (MRI). An attractive alternative contrast agent is composed of gadolinium oxide nanoparticles as they have shown to provide enhanced contrast and, in principle, more straightforward molecular capping possibilities. In this study, we report a new, simple, and polyol-free way of synthesizing 4-5-nm-sized Gd 2O 3 nanoparticles at room temperature, with high stability and water solubility. The nanoparticles induce high-proton relaxivity compared to Gd-DTPA showing r 1 and r 2 values almost as high as those for free Gd 3+ ions in water. The Gd 2O 3 nanoparticles are capped with acetate and carbonate groups, as shown with infrared spectroscopy, near-edge X-ray absorption spectroscopy, X-ray photoelectron spectroscopy and combined thermogravimetric and mass spectroscopy analysis. Interpretation of infrared spectroscopy data is corroborated by extensive quantum chemical calculations. This nanomaterial is easily prepared and has promising properties to function as a core in a future contrast agent for MRI.
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| 4. |
- Ahrén, Maria, et al.
(författare)
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Synthesis and Characterization of PEGylated Gd2O3 Nanoparticles for MRI Contrast Enhancement
- 2010
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Ingår i: Langmuir. - : American Chemical Society (ACS). - 0743-7463 .- 1520-5827. ; 26:8, s. 5753-5762
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Tidskriftsartikel (refereegranskat)abstract
- Recently, much attention has been given to the development of biofunctionalized nanoparticles with magnetic properties for novel biomedical imaging. Guided, smart, targeting nanoparticulate magnetic resonance imaging (MRI) contrast agents inducing high MRI signal will be valuable tools for future tissue specific imaging and investigation of molecular and cellular events. In this study. We report a new design of functionalized ultrasmall rare earth based nanoparticles to be used as a positive contrast agent in NI RI. The relaxivity is compared to commercially available Gd based chelates. The synthesis, PEGylation, and dialysis of small (3-5 nm) gadolinium oxide (DEG-Gd2O3) nanoparticles are presented. The chemical and physical properties of the nanomaterial were investigated with Fourier transform infrared spectroscopy. X-ray photoelectron spectroscopy, transmission electron microscopy, and dynamic light scattering. Neutrophil activation after exposure to this nanomaterial was studied by means of fluorescence microscopy. The proton relaxation times as a function of dialysis time and functionalization were measured at 1.5 T. A capping procedure introducing stabilizing properties was designed and verified, and the dialysis effects were evaluated. A higher proton relaxivity was obtained for as-synthesized diethylene glycol (DEG)-Gd2O3 nanoparticles compared to commercial Gd-DTPA. A slight decrease of the relaxivity for as-synthesized DEG-Gd2O3 nanoparticles as a function of dialysis time was observed. The results for functionalized nanoparticles showed a considerable relaxivity increase for particles dialyzed extensively with r(1) and r(2) values approximately 4 times the corresponding values for Gd-DTPA. The microscopy study showed that PEGylated nanoparticles do not activate neutrophils in contrast to uncapped Gd2O3. Finally, the nanoparticles are equipped with Rhodamine to show that our PEGylated nanoparticles are available for further coupling chemistry, and thus prepared for targeting purposes. The long term goal is to design a powerful, directed contrast agent for MRI examinations with specific targeting possibilities and with properties inducing local contrast, that is. an extremely high MR signal at the cellular and molecular level.
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| 5. |
- Björk, Linnea, et al.
(författare)
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Amino-Acid Side-Chain Nanoarchitectonics for Tuning the Chiroptical Properties and Supramolecular Structure of Pentameric Oligothiophenes
- 2024
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Ingår i: ChemPhotoChem. - : WILEY-V C H VERLAG GMBH. - 2367-0932.
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Tidskriftsartikel (refereegranskat)abstract
- Oligothiophenes with specific photophysical properties and molecular organization are of great interest, since this class of materials are used in organic electronics and bioelectronics, as well as biosensing. Herein, 8 different pentameric oligothiophenes, denoted proteophenes, with different amino acid substitution patterns at distinct positions along the thiophene backbone were investigated. Spectroscopic and microscopic studies of the ligands revealed the formation of optically active self-assembled materials under acidic or basic conditions. The distinct photophysical characteristics, including induced circular dichroism, as well as the supramolecular structures of the assemblies deduced from light scattering and transmission electron microscopy, were highly influenced by the positioning of distinct amino acid moieties along the thiophene backbone. Proteophenes functionalized with only glutamate residues or these functionalities in combination with hydrophobic valine moieties formed fibrillar structures with excellent chiroptical properties under acidic conditions. In addition, the amino acid functionality at the beta-position of distinct thiophene moieties influenced the induced circular dichroism pattern observed from the proteophenes. Overall, the obtained results demonstrate how changes in the position of various amino acid functionalities, as well as the chemical nature of the amino acid side chain functionality greatly affect the optical properties as well as the architecture of the self-assembled materials. Self-assembled Proteophenes. Oligothiophenes with distinct amino acid side-chain functionalities along the conjugated backbone displayed distinct chiroptical and structural properties in acidic or alkaline solutions. The distinct photophysical characteristics, as well as the supramolecular structures of the assemblies were highly influenced by the chemical nature of the amino acid, as well as the positioning of distinct amino acid moieties along the thiophene backbone.image
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| 6. |
- Chen, Zhiwen, et al.
(författare)
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Integrated Design of Hierarchical CoSnO3@NC@MnO@NC Nanobox as Anode Material for Enhanced Lithium Storage Performance
- 2020
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Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 12:17, s. 19768-19777
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Tidskriftsartikel (refereegranskat)abstract
- Transition-metal oxides (TMOs) are potential candidates for anode materials of lithium-ion batteries (LIBs) due to their high theoretical capacity (similar to 1000 mA h/g) and enhanced safety from suppressing the formation of lithium dendrites. However, the poor electron conductivity and the large volume expansion during lithiation/delithiation processes are still the main hurdles for the practical usage of TMOs as anode materials. In this work, the CoSnO3@NC@ MnO@NC hierarchical nanobox (CNMN) is then proposed and fabricated to solve those issues. The as-prepared nanobox contains hollow cubic CoSnO3 as a core and dual N-doped carbon-"sandwiched" MnO particles as a shell. As anode materials of LIBs, the hollow and carbon interlayer structures effectively accommodate the volume expansion while dual active TMOs of CoSnO3 and Notably, the dual-layer structure of N-doped carbons plays a critical functional role MnO efficiently increase the specific capacity. in the incorporated composites, where the inner layer serves as a reaction substrate and a spatial barrier and the outer layer offers electron conductivity, enabling more effective involvement of active anode materials in lithium storage, as well as maintaining their high activity during lithium cycling. Subsequently, the as-prepared CNMN exhibits a high specific capacity of 1195 mA h/g after the 200th cycle at 0.1C and an excellent stable reversible capacity of about 876 mA h/g after the 300th cycle at 0.5C with only 0.07 mA h/g fade per cycle after 300 cycles. Even after a 250 times fast charging/discharging cycle both at SC, it still retains a reversible capacity of 422.6 mA h/g. We ascribe the enhanced lithium storage performances to the novel hierarchical architectures achieved from the rational design.
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| 7. |
- de Oliveira, Sergio, et al.
(författare)
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Failure prediction in fiber-reinforced composites based on continuum damage mechanics
- 2019
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Ingår i: Proceedings - 7th ECCOMAS THEMATIC CONFERENCE ON THE MECHANICAL RESPONSE OF COMPOSITES.
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Konferensbidrag (refereegranskat)abstract
- The paper presents an approach to intra/inter-laminar failure modeling of fiber reinforced composites using continuum damage. The intra-laminar damage model is based on elastic damage, focusing propagation of damage for compression dominated loadings. A special feature is the study on ply elasticity, induced by graphene enhancement of the polymer matrix linked to the damage evolution. The results shows that the considered intra-laminar composite response is only slight affected by the graphene. The open hole compression test involves mechanisms of both intra- and interlaminar failure. The results show a fairly good correlation between the experiments and the proposed model.
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| 8. |
- Enander, Karin, 1972-, et al.
(författare)
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A peptide-based, ratiometric biosensor construct for direct fluorescence detection of a protein analyte
- 2008
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Ingår i: Bioconjugate chemistry. - : American Chemical Society (ACS). - 1043-1802 .- 1520-4812. ; 19:9, s. 1864-1870
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Tidskriftsartikel (refereegranskat)abstract
- We present the design, synthesis, and functional evaluation of peptide-based fluorescent constructs for wavelength-ratiometric biosensing of a protein analyte. The concept was shown using the high-affinity model interaction between the 18 amino acid peptide pTMVP and a recombinant antibody fragment, Fab57P. pTMVP was functionalized in two different positions with 6-bromomethyl-2-(2-furanyl)-3-hydroxychromone, an environmentally sensitive fluorophore with a two-band emission. The equilibrium dissociation constant of the interaction between pTMVP and Fab57P was largely preserved upon labeling. The biosensor ability of the labeled peptide constructs was evaluated in terms of the relative intensity change of the emission bands from the normal (N*) and tautomer (T*) excited-state species of the fluorophore (IN*/IT*) upon binding of Fab57P. When the peptide was labeled in the C terminus, the IN*/I T* ratio changed by 40% upon analyte binding, while labeling close to the residues most important for binding resulted in a construct that completely lacked ratiometric biosensor ability. Integrated biosensor elements for reagentless detection, where peptides and ratiometric fluorophores are combined to ensure robustness in both recognition and signaling, are expected to become an important contribution to the design of future protein quantification assays in immobilized formats. © 2008 American Chemical Society.
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| 9. |
- Hu, Zhangjun, et al.
(författare)
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Highly Water-Dispersible Surface-Modified Gd2O3 Nanoparticles for Potential Dual-Modal Bioimaging
- 2013
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Ingår i: Chemistry - A European Journal. - : Wiley-VCH Verlagsgesellschaft. - 0947-6539 .- 1521-3765. ; 19:38, s. 12658-12667
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Tidskriftsartikel (refereegranskat)abstract
- Water-dispersible and luminescent gadolinium oxide (GO) nanoparticles (NPs) were designed and synthesized for potential dual-modal biological imaging. They were obtained by capping gadolinium oxide nanoparticles with a fluorescent glycol-based conjugated carboxylate (HL). The obtained nanoparticles (GO-L) show long-term colloidal stability and intense blue fluorescence. In addition, L can sensitize the luminescence of europium(III) through the so-called antenna effect. Thus, to extend the spectral ranges of emission, europium was introduced into L-modified gadolinium oxide nanoparticles. The obtained Eu-III-doped particles (Eu:GO-L) can provide visible red emission, which is more intensive than that without L capping. The average diameter of the monodisperse modified oxide cores is about 4nm. The average hydrodynamic diameter of the L-modified nanoparticles was estimated to be about 13nm. The nanoparticles show effective longitudinal water proton relaxivity. The relaxivity values obtained for GO-L and Eu:GO-L were r(1)=6.4 and 6.3s(-1)mM(-1) with r(2)/r(1) ratios close to unity at 1.4T. Longitudinal proton relaxivities of these nanoparticles are higher than those of positive contrast agents based on gadolinium complexes such as Gd-DOTA, which are commonly used for clinical magnetic resonance imaging. Moreover, these particles are suitable for cellular imaging and show good biocompatibility.
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| 10. |
- Huang, Shoushuang, et al.
(författare)
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Fabrication of multi-layer CoSnO3@carbon-caged NiCo2O4 nanobox for enhanced lithium storage performance
- 2021
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Ingår i: Chemical Engineering Journal. - : Elsevier Science SA. - 1385-8947 .- 1873-3212. ; 410
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Tidskriftsartikel (refereegranskat)abstract
- Mixed transition metal oxides (MTMOs) are deemed as promising anode materials for lithium-ion batteries (LIBs) because of the high theoretical capacity and low cost. However, the low electrical conductivity, agglomeration effects, and huge volume variation during discharging/charging still seriously restrict the actual applications of MTMOs as anode materials. Herein, a novel core-shell structure of CoSnO3@carbon-caged NiCo2O4 nanobox (CNC) is rationally designed. It starts from the preparation of CoSnO3@ZIF-67 core-shell nanocubes, followed by chemical etching/anion exchange, dopamine coating and carbonization at high temperature in sequence. It is shown that the CNC achieves high activities from the applied MTMOs components, excellent relief of volume variation from the unique double hollow structure, improved conductivity and inhabited aggregations from the uniform-coated outmost carbon shell, and effective ion/electron transfer rates from the synergetic effects. As a result, the CNC exhibits a discharge capacity of 1548 mA h g(-1) at the first cycle and a retention capacity of 992 mA h g(-1) after 100 cycles at 0.1 A g(-1). In addition, it exhibits a high reversible capacity of about 670 mA h g(-1) after 500 cycles at a current density of 1 A g(-1). The improved Li+ storage performances of CNC demonstrates that such rational design of double hollow structure could be a novel strategy to apply MTMOs as anode materials of LIBs.
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