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This paper describes the evaluation of carbon paper electrodes for supercapacitor applications. The electrodes are based on carbon micro-fiber paper modified with active material consisting of layers of silver nano-particulate ink and a nanocomposite of multi-walled carbon nanotubes and silver nano-particulate ink. The electrodes were characterized microscopically and electrically. Current–voltage studies revealed a consistent Ohmic behavior of the electrode when modified with different nanostructured active material. Among the active materials incorporated into the electrode, a nanocomposite of carbon nanotubes and silver nano-particulate ink significantly improved capacitance. The paper electrodes can be used for lightweight and ultrathin supercapacitors and other portable energy applications.

TiO2 nanopigments in two pure crystallographic forms (anatase and rutile) have been synthesized successfully by two methods; hydrothermal and hydrolysis. The produced pigments from the two methods were investigated physicochemically by several analyses tools. Then they were applied in paper coating mixtures and their influence on coated paper properties was systematically investigated. XRD and FTIR investigations showed that the prepared pigments using hydrothermal method at 100 and 120 °C were a mixture of anatase and brookite and pure anatase, respectively, whereas hydrolysis method produced pure rutile phase pigment. TEM investigation showed that the crystallite size of anatase, mixture of anatase and brookite and rutile samples are 6.2, 11.7, and 9.2 nm, respectively. BET studies proved that anatase pigment has 140.74 m2/g, 0.237 cc/g and 18.33 A, whereas rutile has 60.621 m2/g, 0.122 cc/g and 14.669 A, surface area, pore volume and pore diameter, respectively. UV–Vis absorption and PL emission characteristics of the prepared pigments showed that the energy gaps for anatase, mixture of anatase and brookite and rutile are 3.36, 3.30 and 3.37 eV, respectively. The addition of the prepared nanopigments in conjugation with clay in coating mixture increased both brightness and opacity of the coated papers. The greatest effect was obtained upon using rutile nanopigment. Also there was a significant decrease in coated paper roughness while the air permeance started to decrease then increased at 50 % addition levels. In all coated paper, rutile pigment showed the highest enhancement effect on coated paper properties.

The interactions between dendrimers and different types of drugs are nowadays one of the most actively investigated areas of the pharmaceutical sciences. The interactions between dendrimers and drugs can be divided into: internal encapsulation, external electrostatic interaction, and covalent conjugation. In the present study, we investigated the potential of poly(amidoamine) (PAMAM) dendrimers for solubility of four iminodiacetic acid derivatives. We reported that PAMAM dendrimers contribute to significant solubility enhancement of iminodiacetic acid analogues. The nature of the dendrimer-drug complexes was investigated by (1)H NMR and 2D-NOESY spectroscopy. The (1)H NMR analysis proved that the water-soluble supramolecular structure of the complex was formed on the basis of ionic interactions between terminal amine groups of dendrimers and carboxyl groups of drug molecules, as well as internal encapsulation. The 2D-NOESY analysis revealed interactions between the primary amine groups of PAMAM dendrimers and the analogues of iminodiacetic acid. The results of solubility studies together with (1)H NMR and 2D-NOESY experiments suggest that the interactions between PAMAM dendrimers of generation 1-4 and derivatives of iminodiacetic acid are based on electrostatic interactions and internal encapsulation.Electronic supplementary material The online version of this article (doi:10.1007/s10867-012-9277-5) contains supplementary material, which is available to authorized users.

Rapid pr ogress in graphene-based applications is calling for new processing techniques for creating graphene components with different shapes, sizes, and edge structures. Here we report a controlled cutting process for graphene sheets, using nickel nanoparticles as a knife that cuts with nanoscale precision. The cutting proceeds via catalytic hydrogenation of the graphene lattice, and can generate graphene pieces with specifi c zigzag or armchair edges. The size of the nanoparticle dictates the edge structure that is produced during the cutting. The cutting occurs along straight lines and along symmetry lines, defined by angles of 60o or 120o, and is defl ected at free edges or defects, allowing practical control of graphene nano-engineering.

High-rate anode materials for lithium-ion batteries are desirable for applications that require high power density. We demonstrate the advantageous rate capability of few-layered graphene nanosheets, with widths of 100–200 nm, over micro-scale graphene nanosheets. Possible reasons for the better performance of the former include their smaller size and better conductivity than the latter. Combination of SnO2 nanoparticles with graphene was used to further improve the gravimetric capacities of the electrode at high charge-discharge rates. Furthermore, the volumetric capacity of the composites was substantially enhanced compared to pristine graphene due to the higher density of the composites.

Graphene oxide (GO) thin films were prepared by solution-casting of non-reduced suspension on glass substrates at ambient conditions. Films were rendered to conductive both with hydrazine treatment and annealing and the results were compared. Annealed films treated without hydrazine revealed superiority over the others. Surface morphology of these films showed very smooth film texture as seen by scanning electron microscope and atomic force microscope. Different optical and electrical parameters were analyzed. Band gap enhanced from 1.25 to 2.4 eV as the solution concentration was decreased where the transmittance increased. This work, in particular represents a straight forward approach compared to other studies to achieve device-quality GO thin films and the findings are important for various optoelectronic applications.

Using the atomic force microscope, we have investigated the nanoscale mechanical response of the attachment adhesive of the terrestrial alga Prasiola linearis (Prasiolales, Chlorophyta). We were able to locate and extend highly ordered mechanical structures directly from the natural adhesive matrix of the living plant. The in vivo mechanical response of the structured biopolymer often displayed the repetitive sawtooth force-extension characteristics of a material exhibiting high mechanical strength at the molecular level. Mechanical and histological evidence leads us to propose a mechanism for mechanical strength in our sample based on amyloid fibrils. These proteinaceous, pleated beta-sheet complexes are usually associated with neurodegenerative diseases. However, we now conclude that the amyloid protein quaternary structures detected in our material should be considered as a possible generic mechanism for mechanical strength in natural adhesives.

We report a facile approach to synthesize narrow and long graphene nanoribbons (GNRs) by sonochemically cutting chemically derived graphene sheets (GSs). The yield of GNRs can reach ~5 wt% of the starting GSs. The resulting GNRs are several micrometers in length, with ~75% being single-layer, and ~40% being narrower than 20 nm in width. A chemical tailoring mechanism involving oxygen-unzipping of GSs under sonochemical conditions is proposed on the basis of experimental observations and previously reported theoretical calculations; it is suggested that the formation and distribution of line faults on graphite oxide and GSs play crucial roles in the formation of GNRs. These results open up the possibilities of the large-scale synthesis and various technological applications of GNRs.

We report the synthesis of isotopically-labeled graphite films on nickel substrates by using cold-wall chemical vapor deposition (CVD). During the synthesis, carbon from 12C- and 13C-methane was deposited on, and dissolved in, a nickel foil at high temperature, and a uniform graphite film was segregated from the nickel surface by cooling the sample to room temperature. Scanning and transmission electron microscopy, micro-Raman spectroscopy, and X-ray diffraction prove the presence of a graphite film. Monolayer graphene films obtained from such isotopically-labeled graphite films by mechanical methods have electron mobility values greater than 5000 cm2·V−1·s−1 at low temperatures. Furthermore, such films exhibit the half-integer quantum Hall effect over a wide temperature range from 2 K to 200 K, implying that the graphite grown by this cold-wall CVD approach has a quality as high as highly oriented pyrolytic graphite (HOPG). The results from transport measurements indicate that 13C-labeling does not significantly affect the electrical transport properties of graphene.

An individual suspended graphene sheet was connected to a scanning tunneling microscopy probe inside a transmission electron microscope, and Joule heated to high temperatures. At high temperatures and under electron beam irradiation, the few-layer graphene sheets were removed layer-by-layer in the viewing area until a monolayer graphene was formed. The layer-by-layer peeling was initiated at vacancies in individual graphene layers. The vacancies expanded to form nanometer-sized holes, which then grew along the perimeter and propagated to both the top and bottom layers of a bilayer graphene joined by a bilayer edge. The layer-by-layer peeling was induced by atom sublimation caused by Joule heating and facilitated by atom displacement caused by high-energy electron irradiation, and may be harnessed to control the layer thickness of graphene for device applications.

Gold nanoparticles (Au NPs) were prepared by direct current atmospheric pressure glow microdischarge (dc-μAPGD) generated between a miniature argon flow microjet and a flowing liquid cathode. The applied discharge system was operated in a continuous flow liquid mode. The influence of various stabilizers added to the solution of the liquid cathode, i.e., gelatin (GEL), polyvinylpyrrolidone (PVP), or polyvinyl alcohol (PVA), as well as the concentration of the Au precursor (chloroauric acid, HAuCl4) in the solution on the production growth of Au NPs was investigated. Changes in the intensity of the localized surface plasmon resonance (LSPR) band in UV/Vis absorption spectra of solutions treated by dc-μAPGD and their color were observed. The position and the intensity of the LSPR band indicated that relatively small nanoparticles were formed in solutions containing GEL as a capping agent. In these conditions, the maximum of the absorption LSPR band was at 531, 534, and 535 nm, respectively, for 50, 100, and 200 mg L−1 of Au. Additionally, scanning electron microscopy (SEM) and dynamic light scattering (DLS) were used to analyze the structure and the morphology of obtained Au NPs. The shape of Au NPs was spherical and uniform. Their mean size was ca. 27, 73, and 92 nm, while the polydispersity index was 0.296, 0.348, and 0.456 for Au present in the solution of the flowing liquid cathode at a concentration of 50, 100, and 200 mg L−1, respectively. The production rate of synthesized Au NPs depended on the precursor concentration with mean values of 2.9, 3.5, and 5.7 mg h−1, respectively.

The aim of the work was to characterise coal tar pitch (CTP) modified with selected nanoparticles as a binder precursor for the manufacture of synthetic carbon materials. Different factors influencing the preliminary preparative steps in the preparation of homogenous nanoparticle/CTP composition were studied. Graphene flakes, carbon black and nano-sized silicon carbide were used to modify CTP. Prior to introducing them into liquid CTP, nanoparticles were subjected to sonication. Various dispersants were used to prepare the suspensions, i.e. water, ethanol, dimethylformamide (DMF) and N-methylpyrrolidone (NMP).The results showed that proper dispersant selection is one of the most important factors influencing the de-agglomeration process of nanoparticles. DMF and NMP were found to be effective dispersants for the preparation of homogenous nanoparticle-containing suspensions. The presence of SiC and carbon black nanoparticles in the liquid pitch during heat treatment up to 2000 °C leads to the inhibition of crystallite growth in carbon residue.

Carbon-encapsulated iron nanoparticles (CEINs) are emerging as promising biomedical tools due to their unique physicochemical properties. In this study, the cytotoxic effect of CEINs (the mean diameter distribution ranges 46–56 nm) has been explored by MTT, LDH leakage, Calcein-AM/propidium iodide (PI) and Annexin V-FITC/PI assays in human melanoma (HTB-140), mouse melanoma (B16-F10) cells, and human dermal fibroblasts (HDFs). The results demonstrated that CEINs produce mitochondrial and cell membrane cytotoxicities in a dose (0.0001–100 μg/ml)-dependent manner. Moreover, the studies elucidated some differences in cytotoxic effects between CEINs used as raw and purified materials composing of the carbon surface with acidic groups. Experiments showed that HTB-140 cells are more sensitive to prone early apoptotic events due to raw CEINs as compared to B16-F10 or HDF cells, respectively. Taken together, these results suggest that the amount of CEINs administered to cells and the composition of CEINs containing different amounts of iron as well as the carbon surface modification type is critical determinant of cytotoxic responses in both normal and cancer (melanoma) cells. Electronic supplementary material The online version of this article (doi:10.1007/s11051-013-1835-7) contains supplementary material, which is available to authorized users.

Pure cubic phase ultra-small α-NaYF4:4 % Eu3+ colloidal nanoparticles were synthesized by thermal decomposition reaction using three various capping ligands, i.e., oleic acid, trioctylphosphine oxide, and hexadecylamine. To expose as many Eu3+ ions as possible to interactions with the surface-bounded ligands, the nanoparticles were fabricated to have the diameters below 10 nm. The geometrical structure and properties of surface ligands needed for qualitative estimation of their influence on spectroscopic features of the investigated Eu3+ doped nanoparticles were obtained from DFT quantum-chemical calculations. Significant changes of luminescence spectra shapes and luminescence lifetime values were observed upon changes in the local chemical environment. We show that the ratio R = 5D0 → 7F1/5D0 → 7F2 of the intensities of the forced electric dipole (J = 2) and magnetic dipole (J = 1) transitions in the synthesized Eu3+ doped nanoparticles is highly sensitive to the type of ligand present on the nanoparticle surface. Similarly, 5D0 luminescence lifetimes are found to be sensitive to the refractive index, and also to the dielectric constant of ligands used during the synthesis to coat nanoparticles surface. We argue that the photophysical and electro-optical properties of colloidal Eu3+ doped inorganic nanoparticles show hyper-sensitive response to the chemical surroundings in the close vicinity of the nanoparticle itself. The behavior of both steady-state luminescence and its kinetics demonstrates the potential suitability of the studied nanoparticles for constructing self-referencing optical nano-sensors. Electronic supplementary material The online version of this article (doi:10.1007/s11051-013-1707-1) contains supplementary material, which is available to authorized users.

The ultrasonic propagation in the water-based magnetic fluid with doubled layered surfactant shell was studied. The measurements were carried out both in the presence as well as in the absence of the external magnetic field. The thickness of the surfactant shell was evaluated by comparing the mean size of magnetic grain extracted from magnetization curve with the mean hydrodynamic diameter obtained from differential centrifugal sedimentation method. The thickness of surfactant shell was used to estimate volume fraction of the particle aggregates consisted of magnetite grain and surfactant layer. From the ultrasonic velocity measurements in the absence of the applied magnetic field, the adiabatic compressibility of the particle aggregates was determined. In the external magnetic field, the magnetic fluid studied in this article becomes acoustically anisotropic, i.e., velocity and attenuation of the ultrasonic wave depend on the angle between the wave vector and the direction of the magnetic field. The results of the ultrasonic measurements in the external magnetic field were compared with the hydrodynamic theory of Ovchinnikov and Sokolov (velocity) and with the internal chain dynamics model of Shliomis, Mond and Morozov (attenuation).

In the current work carbon-supported nanoscale zero-valent iron particles (CS nZVI), synthesised by the vacuum heat treatment of ferric citrate trihydrate absorbed onto carbon black, have been tested for the removal of uranium (U) from natural and synthetic waters. Two types of CS nZVI were tested, one vacuum annealed at 600 °C for 4 h and the other vacuum annealed at 700 °C for 4 h, with their U removal behaviour compared to nZVI synthesised via the reduction of ferrous iron using sodium borohydride. The batch systems were analysed over a 28-day reaction period during which the liquid and nanoparticulate solids were periodically analysed to determine chemical evolution of the solutions and particulates. Results demonstrate a well-defined difference between the two types of CS nZVI, with greater U removal exhibited by the nanomaterial synthesised at 700 °C. The mechanism has been attributed to the CS nZVI synthesised at 700 °C exhibiting (i) a greater proportion of surface oxide Fe2+ to Fe3+ (0.34 compared to 0.28); (ii) a greater conversion of ferric citrate trihydrate [2Fe(C6H5O7)·H2O] to Fe0; and (iii) a larger surface area (108.67 compared to 88.61 m2 g−1). Lower maximum U uptake was recorded for both types of CS nZVI in comparison with the borohydride-reduced nZVI. A lower decrease in solution Eh and DO was also recorded, indicating that less chemical reduction of U was achieved by the CS nZVI. Despite this, lower U desorption in the latter stages of the experiment (>7 days) was recorded for the CS nZVI synthesised at 700 °C, indicating that carbon black in the CS nZVI is likely to have contributed towards U sorption and retention. Overall, it can be stated that the borohydride-reduced nZVI were significantly more effective than CS nZVI for U removal over relatively short timescales (e.g.

Gold nanoparticles are one of the most used nanomaterials. They are usually synthesized by the reduction of gold(III) chloride. However, the presence of halide ions in the reaction mixture is not always welcome. In some cases, these ions have detrimental influence on the morphology and structure of resulting nanoparticles. Here, we present a simple and halogen-free procedure to prepare gold nanoparticles by reduction of gold(III) oxide in neat oleylamine. The method provides the particles with an average size below 10 nm and dispersity of tens of percent. The process of nanoparticle formation was monitored using UV–Vis spectroscopy. The structure and chemical composition of the nanoparticles was determined by SEM, XPS and EDX. We also proposed the mechanism of reduction of gold(III) oxide based on MS, IR and NMR data. Importantly, the synthetic protocol is general and applicable for the preparation of other coinage metal nanoparticles from the corresponding metal oxides. For instance, we demonstrated that the absence of halogen enables efficient alloying of metals when preparing gold–silver bimetallic nanoparticles. Electronic supplementary material The online version of this article (doi:10.1007/s11051-016-3576-x) contains supplementary material, which is available to authorized users.

In this work, solid polymer nanospheres with their surface tailored for drug adhesion were prepared using a V-shaped microfluidic junction. The biocompatible polymer solutions were infused using two channels of the microfluidic junction which was also simultaneously fed with a volatile liquid, perfluorohexane using the other channel. The mechanism by which the nanospheres are generated is explained using high speed camera imaging. The polymer concentration (5–50 wt%) and flow rates of the feeds (50–300 µl min−1) were important parameters in controlling the nanosphere diameter. The diameter of the polymer nanospheres was found to be in the range of 80–920 nm with a polydispersity index of 11–19 %. The interior structure and surfaces of the nanospheres prepared were studied using advanced microscopy and showed the presence of fine pores and cracks on surface which can be used as drug entrapment locations. Electronic supplementary material The online version of this article (doi:10.1007/s11051-014-2626-5) contains supplementary material, which is available to authorized users.

Sodium fluoride-based β-NaLnF4 nanoparticles (NPs) doped with lanthanide ions are promising materials for application as luminescent markers in bio-imaging. In this work, the effect of NPs doped with yttrium (Y), gadolinium (Gd), europium (Eu), thulium (Tm), ytterbium (Yb) and terbium (Tb) ions on phagocytic activity of monocytes and granulocytes and the respiratory burst was examined. The surface functionalization of

The increasing use of zinc oxide nanoparticles (ZnO-NPs) has raised concerns about their potential hazards to human and environmental health. In this study, the characterization and cytotoxicity of two ZnO-NPs products (Z-COTE and Z-COTE HP1) were investigated. The zinc content of Z-COTE and Z-COTE HP1 was 82.5 ± 7.3 and 80.1 ± 3.5 %, respectively. Both ZnO–NP samples contained sub-cytotoxic levels of iron and copper, and silicon was detected from the surface coating of Z-COTE HP1. All samples were highly agglomerated, and the primary particles appeared as variable polyhedral structures. There was no significant difference in size distribution or average diameter of Z-COTE (53 ± 23 nm) and Z-COTE HP1 (54 ± 26 nm). A dose-dependent cytotoxicity was observed 24 h after exposure to ZnO-NPs, and monocytes were more sensitive than lung epithelial cells or lymphoblasts in both human and mouse cells. There was a significant difference in cytotoxicity between nano- and fine-forms, but only at the threshold cytotoxic dose with cellular metabolism assays. Compared to uncoated ZnO-NPs, the surface coating with triethoxycaprylylsilane marginally attenuated cellular oxidative stress and protected cellular metabolic activity. These results demonstrate the importance of model cell type, dose selection, and cytotoxicity assessment methodology to accurately evaluate the potential toxicity of various nanoparticles in vitro.

The synthesis, morphological characterization, and optical properties of colloidal, Eu(III) doped Gd2O3 nanoparticles with different sizes and shapes are presented. Utilizing wet chemical techniques and various synthesis routes, we were able to obtain spherical, nanodisk, nanotripod, and nanotriangle-like morphology of Gd2O3:Eu3+ nanoparticles. Various concentrations of Eu3+ ions in the crystal matrix of the nanoparticles were tested in order to establish the levels at which the concentration quenching effect is negligible. Based on the luminescence spectra, luminescence lifetimes and optical parameters, which were calculated using the simplified Judd–Ofelt theory, correlations between the Gd2O3 nanoparticles morphology and Eu3+ ions luminescence were established, and allowed to predict the theoretical maximum quantum efficiency to reach from 61 to 98 %. We have also discussed the impact of the crystal structure of Gd2O3 nanoparticles, as well as coordinating environment of luminescent ions located at the surface, on the emission spectra. With the use of a tunable femtosecond laser system and the Z-scan measurement technique, the values of the effective two-photon absorption cross-section in the wavelength range from 550 to 1,200 nm were also calculated. The nonlinear optical measurements revealed maximum multi-photon absorption in the wavelength range from 600 to 750 nm.

Systems for studying the toxicity of metal aggregates on the airways are normally not suited for evaluating the effects of individual particle characteristics. This study validates a set-up for toxicological studies of metal aggregates using an air–liquid interface approach. The set-up used a spark discharge generator capable of generating aerosol metal aggregate particles and sintered near spheres. The set-up also contained an exposure chamber, The Nano Aerosol Chamber for In Vitro Toxicity (NACIVT). The system facilitates online characterization capabilities of mass mobility, mass concentration, and number size distribution to determine the exposure. By dilution, the desired exposure level was controlled. Primary and cancerous airway cells were exposed to copper (Cu), palladium (Pd), and silver (Ag) aggregates, 50–150 nm in median diameter. The aggregates were composed of primary particles

Systematic studies of silver nanoparticle synthesis in a continuous-flow single-mode microwave reactor using polyol process were performed, revealing that the synthesis is exceptionally effective to give very small metal particles at full reaction yield and very high productivity. Inlet concentration of silver nitrate or silver acetate, applied as metal precursors, varied between 10 and 50 mM, and flow rates ranged from 0.635 to 2.5 dm3/h, to give 3–24 s reaction time. Owing to its much higher reactivity, silver acetate was shown to be far superior substrate for the synthesis of small (10–20 nm) spherical silver nanoparticles within a few seconds. Its restricted solubility in ethylene glycol, applied as the solvent and reducing agent, appeared to be vital for effective separation of the stage of particle growth from its nucleation to enable rapid synthesis of small particles in a highly loaded system. This was not possible to obtain using silver nitrate. All the observations could perfectly be explained by a classical LaMer–Dinegar model of NPs’ formation, but taking into account also nonisothermal character of the continuous-flow process and acetate dissolution in the reaction system. The performed studies indicate an optimal strategy for the high-yield fabrication of metal particles using polyol method.

Journal of Nanoparticle Research, 16 (7), ISSN:1388-0764, ISSN:1572-896X

In the presented work, amphiphilic nanoparticles based on chitosan and carboxy-enriched polylactic acid have been prepared to improve the stability of the pro-drug temozolomide in physiological media by encapsulation. The carrier, with a diameter in the range of 150–180 nm, was able to accommodate up to 800 μg of temozolomide per mg of polymer. The obtained formulation showed good stability in physiological condition and preparation media up to 1 month. Temozolomide loaded inside the carrier exhibited greater stability than the free drug, in particular in simulated physiological solution at pH 7.4 where the hydrolysis in the inactive metabolite was clearly delayed. CS-SPLA nanoparticles demonstrated a pH-dependent TMZ release kinetics with the opportunity to increase or decrease the rate. Mass spectroscopy, UV-Vis analysis, and in vitro cell tests confirmed the improvement in temozolomide stability and effectiveness when loaded into the polymeric carrier, in comparison with the free drug. © 2017, The Author(s)., 15-08287Y, GACR, Grantová Agentura České Republiky; 15-08287Y, GAČR, Grantová Agentura České Republiky; CZ.1.05/2.1.00/19.0409, MŠMT, Ministerstvo Školství, Mládeže a Tělovýchovy; LO1504, MŠMT, Ministerstvo Školství, Mládeže a Tělovýchovy, Czech Science Foundation [15-08287Y]; Ministry of Education, Youth and Sports of the Czech Republic [LO1504, CZ.1.05/2.1.00/19.0409]; Internal Grant Agency of the Tomas Bata University in Zlin [IGA/CPS/2016/004]

Radiolabelling of industrially manufactured nanoparticles is useful for nanoparticle dosimetry in biodistribution or cellular uptake studies for hazard and risk assessment. Ideally for such purposes, any chemical processing post production should be avoided as it may change the physico-chemical characteristics of the industrially manufactured species. In many cases, proton irradiation of nanoparticles allows radiolabelling by transmutation of a tiny fraction of their constituent atoms into radionuclides. However, not all types of nanoparticles offer nuclear reactions leading to radionuclides with adequate radiotracer properties. We describe here a process whereby in such cases nanoparticles can be labelled with 7Be, which exhibits a physical half-life of 53.29 days and emits γ-rays of 478 keV energy, and is suitable for most radiotracer studies. 7Be is produced via the proton-induced nuclear reaction 7Li(p,n)7Be in a fine-grained lithium compound with which the nanoparticles are mixed. The high recoil energy of 7Be atoms gives them a range that allows the 7Be-recoils to be transferred from the lithium compound into the nanoparticles by recoil implantation. The nanoparticles can be recovered from the mixture by dissolving the lithium compound and subsequent filtration or centrifugation. The method has been applied to radiolabel industrially manufactured SiO2 nanoparticles. The process can be controlled in such a way that no alterations of the 7Be-labelled nanoparticles are detectable by dynamic light scattering, X-ray diffraction and electron microscopy. Moreover, cyclotrons with maximum proton energies of 17–18 MeV that are available in most medical research centres could be used for this purpose.

Ultrafine particles (UFP) have been postulated to significantly contribute to the adverse health effects associated with exposure to particulate matter (PM). Due to their extremely small size (aerodynamic diameter

Granulometry is the regulatory category where the differences between traditional materials and nanomaterials culminate. Reported herein is a careful validation of methods for the quantification of dispersability and size distribution in relevant media, and for the classification according to the EC nanodefinition recommendation. Suspension-based techniques can assess the nanodefinition only if the material in question is reasonably well dispersed. Using dispersed material of several chemical compositions (organic, metal, metal-oxide) as test cases we benchmark analytical ultracentrifugation (AUC), dynamic light scattering (DLS), hydrodynamic chromatography, nanoparticle tracking analysis (NTA) against the known content of bimodal suspensions in the commercially relevant range between 20 nm and a few microns. The results validate fractionating techniques, especially AUC, which successfully identifies any dispersed nanoparticle content from 14 to 99.9 nb% with less than 5 nb% deviation. In contrast, our screening casts severe doubt over the reliability of ensemble (scattering) techniques and highlights the potential of NTA to develop into a counting upgrade of DLS. The unique asset of centrifuges with interference, X-ray or absorption detectors—to quantify the dispersed solid content for each size interval from proteins over individualized nanoparticles up to agglomerates, while accounting for their loose packing—addresses also the adsorption/depletion of proteins and (de-)agglomeration of nanomaterials under cell culture conditions as tested for toxicological endpoints.

The functionalization of silica-coated Fe3O4 magnetic nanoparticles (Fe3O4@SiO2) using chlorosulfonic acid were afforded sulfonic acid-functionalized magnetic Fe3O4 nanoparticles (Fe3O4@SiO2–SO3H) that can be applied as an organic–inorganic hybrid heterogeneous catalyst. The used Fe3O4 magnetic nanoparticles are 18–30 nm sized that was rapidly functionalized and can be used as catalyst in organic synthesis. The prepared nanoparticles were characterized by X-ray diffraction analysis, magnetization curve, scanning electron microscope, dynamic laser scattering, and FT-IR measurements. The resulting immobilized catalysts have been successfully used in the synthesis of 1,8‐dioxo-octahydroxanthene derivatives under solvent free condition. This procedure has many advantages such as; a much milder method, a shorter reaction time, a wide range of functional group tolerance, and absence of any tedious workup or purification. Other remarkable features include the catalyst can be reused at least five times without any obvious change in its catalytic activity. This procedure also avoids hazardous reagents/solvents, and thus can be an eco-friendly alternative to the existing methods. Graphical Abstract A highly efficient nano-Fe3O4 encapsulated-silica particles bearing sulfonic acid groups as a solid acid catalyst for synthesis of 1,8-dioxo-octahydroxanthene derivatives Electronic supplementary material The online version of this article (doi:10.1007/s11051-013-2026-2) contains supplementary material, which is available to authorized users.

Here, we present our work on preparing a novel nanomaterial composed of inorganic binding peptides and magnetic nanoparticles for inorganic mining. Two previously selected and well-characterized gold-binding peptides from cell surface display, AuBP1 and AuBP2, were exploited. This nanomaterial (AuBP-MNP) was designed to fulfill the following two significant functions: the surface conjugated gold-binding peptide will recognize and selectively bind to gold, while the magnetic nano-sized core will respond and migrate according to the applied external magnetic field. This will allow the smart nanomaterial to mine an individual material (gold) from a pool of mixture, without excessive solvent extraction, filtration, and concentration steps. The working efficiency of AuBP-MNP was determined by showing a dramatic reduction of gold nanoparticle colloid concentration, monitored by spectroscopy. The binding kinetics of AuBP-MNP onto the gold surface was determined using surface plasmon resonance (SPR) spectroscopy, which exhibits around 100 times higher binding kinetics than peptides alone. The binding capacity of AuBP-MNP was demonstrated by a bench-top mining test with gold microparticles. Graphical abstract Electronic supplementary material The online version of this article (doi:10.1007/s11051-017-3752-7) contains supplementary material, which is available to authorized users.

It is unclear whether the antimicrobial activities of silver nanoparticles (AgNPs) are exclusively mediated by the release of silver ions (Ag+) or, instead, are due to combined nanoparticle and silver ion effects. Therefore, it is essential to quantify dissolved Ag in nanosilver suspensions for investigations of nanoparticle toxicity. We developed a method to measure dissolved Ag in Ag+/AgNPs mixtures by combining aggregation of AgNPs with centrifugation. We also describe the reproducible synthesis of stable, uncoated AgNPs. Uncoated AgNPs were quickly aggregated by 2 mM Ca2+, forming large clusters that could be sedimented in a low-speed centrifuge. At 20,100g, the sedimentation time of AgNPs was markedly reduced to 30 min due to Ca2+-mediated aggregation, confirmed by the measurements of Ag content in supernatants with graphite furnace atomic absorption spectrometry. No AgNPs were detected in the supernatant by UV–Vis absorption spectra after centrifuging the aggregates. Our approach provides a convenient and inexpensive way to separate dissolved Ag from AgNPs, avoiding long ultracentrifugation times or Ag+ adsorption to ultrafiltration membranes. Electronic supplementary material The online version of this article (doi:10.1007/s11051-016-3565-0) contains supplementary material, which is available to authorized users.

Droplet formation in the presence of nanoparticles was studied in a T-shaped microfluidic device numerically. Nanoparticles in continuous phase did not influence droplet formation dynamics obviously. Contrarily, the presence of nanoparticles in dispersed phase will influence evidently droplet formation dynamics, likely reasons are the accumulation of nanoparticles at the liquid–liquid interface leading to the variation of interfacial tension and the anisotropy of nanoparticles’ movement at interface. The droplet size decreases almost linearly with increasing of the volume fraction of nanoparticles in dispersed phase when the volume fraction of nanoparticles not exceeding a critical value (about 0.2 %), because very high concentration of nanoparticles results in particle aggregation so as to not decrease interfacial tension so obviously any more. A complicated mechanism of temperature influences on droplet formation may exist combining the variations of effective viscosity and interfacial tension. Discussions on microscopic mechanism of droplet formation in the presence of nanoparticles were carried out.

In this paper, we have investigated the perturbed Chen–Lee–Liu equation which describes the pulse propagation in the optical fbers, under the impact of the inter-modal dispersion, self-steepening and nonlinear dispersion terms. By using the enhanced modifed extended tanh expansion method, bright, singular, periodic singular and periodic bright solitons have been obtained and the efects of the coefcients of the inter-modal dispersion, self-steepening and nonlinear dispersion terms on the soliton’s dynamics have been examined in each case. In this respect, the review in the article has not been studied and reported before. The computations throughout this paper have been fulflled by Maple and also the graphical simulations are demonstrated via Matlab.

In this paper, some analytical solutions for a model of dual-core optical fbers governed by a system of coupled non-linear Schrödinger equations (NLSEs) and the efect of the coefcient of the group velocity dispersion term on the considered model are investigated. The group velocity dispersion (GVD) has a important role in the optical wave propagation. The enhanced modifed extended tanh expansion method (eMETEM) is successfully implemented to the governing model. The NLSE system is turned into a nonlinear ordinary diferential equation (NLODE) via appropriate wave transformations. Supposing that the NLODE has solutions in the form suggested by the method and utilizing the enhanced solutions of the Riccati equation, we gain a nonlinear system of algebraic equations. The solutions of the governing model are obtained after solving the system of algebraic equations. 2D, 3D and contour illustrative fgures for the physical interpretation of the attained solutions are presented. Besides, the result of the investigation, which is related to the efect of the coefcient of the group velocity dispersion term, is presented by supporting the various graphical scheme.

As a new concept in materials design, a variety of strategies have been developed to fabricate optical microlens arrays (MLAs) that enable the miniaturization of optical systems on the micro/nanoscale to improve their characteristic performance with unique optical functionality. In this paper, we introduce a cost-effective and facile fabrication process on a large scale up to ~15 inches via sequential lithographic methods to produce thin and deformable hexagonally arranged MLAs consisting of polydimethylsiloxane (PDMS). Simple employment of oxygen plasma treatment on the prestrained MLAs effectively harnessed the spontaneous formation of highly uniform nanowrinkled structures all over the surface of the elastomeric microlenses. With strain-controlled tunability, unexpected optical diffraction patterns were characterized by the interference combination effect of the microlens and deformable nanowrinkles. Consequently, the hierarchically structured MLAs presented here have the potential to produce desirable spatial arrangements, which may provide easily accessible opportunities to realize microlens-based technology by tunable focal lengths for more advanced micro-optical devices and imaging projection elements on unconventional security substrates.

In this article, we focus on securing the diferent soliton and other solutions in the magneto electro-elastic (MEE) circular rod. The abundant solutions of the nonlinear longitudinal wave equation (NLWE) with dispersion caused by the transverse Poisson’s efect in a long MEE circular rod are obtained using the modifed Sardar sub-equation method (MSSEM). The study of optical solitons’ nonlinear dynamics in MEE media (such as sensors, actuators, and controllers) has piqued researchers’ interest. The wave structures in diferent kinds of solitons, such as bright, dark, singular, bright-dark, bright-singular, complex, and combined, are extracted. In addition, hyperbolic, trigonometric, exponential type and periodic solutions are guaranteed. Nonlinear partial diferential equations (NLPDEs) are wellexplained by the applied technique since it ofers previously derived solutions and also extracts new exact solutions by incorporating the results of multiple procedures. Moreover, in explaining the physical representation of certain solutions, we also plot 3D, 2D, and contour graphs using the corresponding parameter values. This paper’s fndings can enhance the nonlinear dynamical behavior of a given system and demonstrate the efcacy of the employed methodology. We believe that a large number of specialists in engineering models will beneft from this research. The results indicate that the employed algorithm is efective, swift, concise, and applicable to complex systems.

In this paper, we use the Jacobi elliptic function expansion approach to investigate the Hirota-Maccari system which describes the dynamical behaviors of the femto-second soliton pulse in single-mode fbers. As a result, solutions with various structures are developed including dark-bright, dark, single, brilliant, exponential function, and Jacobi elliptic function solutions. In addition, a computer application is used to examine the solutions found on three-dimensional surfaces and two-dimensional visuals.

The application of titanium dioxide (TiO2) in the photovoltaic field is gaining traction as this material can be deployed in doping-free heterojunction solar cells with the role of electron selective contact. For modeling-based optimization of such contact, knowledge of the titanium oxide defect density of states is crucial. In this paper, we report a method to extract the defect density through nondestructive optical measures, including the contribution given by small polaron optical transitions. The presence of both related to oxygen-vacancy defects and polarons is supported by the results of optical characterizations and the evaluation of previous observations resulting in a defect band fixed at 1 eV below the conduction band edge of the oxide. Solar cells employing pulsed laser deposited-TiO2 electron selective contacts were fabricated and characterized. The J-V curve of these cells showed, however, a S-shape, then a detailed analysis of the reasons of such a behavior was carried out. We use a model involving the series of a standard cell equivalent circuit with a Schottky junction in order to explain these atypical performances. A good matching between the experimental measurements and the adopted theoretical model was obtained. The extracted parameters are listed and analyzed to shade light on the reasons behind the low-performance cells.

Optical fibre networks are advancing rapidly to meet growing traffic demands. Security issues, including attack management, have become increasingly important for optical communication networks because of the vulnerabilities associated with tapping light from optical fibre links. Physical layer security often requires restricting access to channels and periodic inspections of link performance. In this paper, we report how quantum communication techniques can be utilized to detect a physical layer attack. We present an efficient method for monitoring the physical layer security of a high-data-rate classical optical communication network using a modulated continuous-variable quantum signal. We describe the theoretical and experimental underpinnings of this monitoring system and the monitoring accuracy for different monitored parameters. We analyse its performance for both unamplified and amplified optical links. The technique represents a novel approach for applying quantum signal processing to practical optical communication networks and compares well with classical monitoring methods. We conclude by discussing the challenges facing its practical application, its differences with respect to existing quantum key distribution methods, and its usage in future secure optical transport network planning., Optical communication security: Sound the quantum alarm A quantum alarm system can detect eavesdropping on optical communication links faster than classical methods. The system was developed by Yupeng Gong and colleagues at the University of Cambridge, UK, and involves transmitting two modes that are indistinguishable to an eavesdropper over the same channel and at the same wavelength. One mode sends a classical data signal and the other sends the security-monitoring quantum modulated signal. The alarm system is low-cost and can easily be used with high data-rate communication links that are hundreds of kilometers long. It can also be used with other encryption methods. The quantum alarm overcomes issues in other attack detection techniques, including quantum key distribution, which is challenging to implement in high data-rate optical communication networks.

This paper presents a new cell culture platform enabling label-free surface-enhanced Raman spectroscopy (SERS) analysis of biological samples. The platform integrates a multilayered metal-insulator-metal nanolaminated SERS substrate and polydimethylsiloxane (PDMS) multiwells for the simultaneous analysis of cultured cells. Multiple cell lines, including breast normal and cancer cells and prostate cancer cells, were used to validate the applicability of this unique platform. The cell lines were cultured in different wells. The Raman spectra of over 100 cells from each cell line were collected and analyzed after 12 h of introducing the cells to the assay. The unique Raman spectra of each cell line yielded biomarkers for identifying cancerous and normal cells. A kernel-based machine learning algorithm was used to extract the high-dimensional variables from the Raman spectra. Specifically, the nonnegative garrote on a kernel machine classifier is a hybrid approach with a mixed nonparametric model that considers the nonlinear relationships between the higher-dimension variables. The breast cancer cell lines and normal breast epithelial cells were distinguished with an accuracy close to 90%. The prediction rate between breast cancer cells and prostate cancer cells reached 94%. Four blind test groups were used to evaluate the prediction power of the SERS spectra. The peak intensities at the selected Raman shifts of the testing groups were selected and compared with the training groups used in the machine learning algorithm. The blind testing groups were correctly predicted 100% of the time, demonstrating the applicability of the multiwell SERS array for analyzing cell populations for cancer research. Researchers in the USA have developed a cell culture platform which enhances spectroscopic analysis, making it possible to carry out molecular profiling of biological samples without any labeling. A team led by Masoud Agah and Wei Zhou of Virginia Tech incorporated nanolaminated plasmonic structures into the surface of a multi-well cell culture plate. This modification improves the performance of Raman spectroscopy, facilitating more sensitive and precise biochemical profiling, and the resulting spectra were analyzed via machine learning. The team tested their approach by using it to discriminate samples of normal breast tissue, breast cancer cells, and prostate cancer cells. The analysis distinguished the cell types with over 90% accuracy. This approach can be used for label-free analysis of diagnostic biomarkers to identify specific cancer subtypes, and further work may make it possible to analyze samples of mixed cells.

In this paper, we consider the model of a nonlinear system subjected simultaneously to a random telegraph noise and a white noise. By using the formulae of differentiation introduced by Shapiro and Loginov (Physica 91:563–574, 1978), an exact equation for the steady state probability distribution of fluctuation in this system is derived. As an example of its application, we calculate analytically the steady state probability distribution of fluctuation and show the existence of noise induced phase transitions (Wodkiewicz et al. in J. Opt. Soc. Am. 1:398–405, 1984a) in Raman Ring Laser. Moreover, we show explicitly the so-called noise reduction considered in Lewenstein and Rzązewski (Opt. Commun. 63:174–178, 1987) for this system. It follows that the Stokes output of this laser tends to the stabilization under influence of the broad-band telegraph pump. This phenomenon could be realized experimentally in a much easer manner than for the case of Gaussian pump, because the construction of the injected telegraph pump signal is much easer than in the case of Gaussian signal. The recent paper is an extended version of Doan and Van (1991).

In this paper, the most recent progress as well as challenges of distributed optical fiber sensing (DOFS) in industrial applications is discussed. Compared to the vast market of sensors used to measure strain or temperature, the success of distributed optical fiber sensing (DOFS) at the industrial level is very limited, at best. One of the reasons for this lack of the wider acceptance is the mismatch between the commercially available systems and actual industrial requirements, especially for the spatial resolution and precision. These requirements are organized and clarified in the paper. It also describes the hybrid Brillouin-Rayleigh system, which exhibits capabilities surpassing those of strain gauges. The principles of the system are illustrated considering the fiber calibration methodology. Formulas required for determining strain, temperature, and hydro-pressure are derived and discussed. Finally, the examples of applications are presented.

This paper presents an innovative and low-cost approach for nondestructive fruit quality analysis. The specialized optical fiber sensor developed and presented in this paper used a monochromatic wavelength, rather than a broad spectrum, to measure the intact carambola (star fruit) intrinsic quality, namely pH and firmness. The main objective of this research was to investigate the two optical fiber sensors used in this work, namely, the optical fiber red system (OF-RS) that operated with the peak sensitivity at 635 nm and the optical fiber near the infrared spectroscopy system (OF-NIRS) that operated with the peak sensitivity at 880 nm. Both systems showed good accuracy in the pH and firmness measurement of the intact carambola with the correlation coefficient R over 0.75, and the measurement results were comparable with those of the commercial spectrometer. The best measurement results were obtained using OF-RS (pH: R = 0.876; the root mean square error (RMSE) = 0.211 pH; firmness: R = 0.872; RMSE = 0.909 kgf).

The aim of the paper is to analyze the effect of velocity slip boundary condition on the flow and heat transfer of non-Newtonian nanofluid over a stretching sheet. The Brownian motion and thermophoresis effects are also considered. The boundary layer equations governed by the partial differential equations are transformed into a set of ordinary differential equations with the help of group theory transformations. The obtained ordinary differential equations are solved by variational finite element method (FEM). The effects of different controlling parameters, namely, the Brownian motion parameter, the thermophoresis parameter, viscoelastic parameter, Prandtl number, Lewis number and the slip parameter on the flow field and heat transfer characteristics are examined. The numerical results for the dimensionless velocity, temperature and nanoparticle volume fraction as well as the reduced Nusselt and Sherwood number have been presented graphically. The present study is of great interest in the fields of coatings and suspensions, cooling of metallic plates, oils and grease, paper production, coal water or coal–oil slurries, heat exchangers’ technology, and materials’ processing and exploiting.

This paper describes the development and applications of a fiber-optic electric current sensing technique with the stable properties and compact, simple, and flexible structure of the sensing device. The special characteristics of the sensors were achieved by use of the special low birefringence fiber as the Faraday-effect sensing element and were also achieved with creation of sensing schemes which matched with the features of the fiber. Making use of the excellent features of the sensing technique, various current monitoring devices and systems were developed and applied practically for the control and maintenance in the electric power facility. In this paper, the design and performance of the sensing devices are introduced first. After that, examples of the application systems practically applied are also introduced, including fault section/point location systems for power transmission cable lines.

This paper investigates the application of distributed optical fiber strain sensors to civil engineering structures, because no other tool can satisfactorily detect the location of the unpredictable phenomenon. In fact, the locations of cracks in the concrete structure are unknown a priori; therefore, a fully distributed sensor is necessary to detect them. The Brillouin optical correlation domain analysis (BOCDA), which offers high spatial resolution by using stimulated Brillouin scattering along the whole length of the optical fiber, is used in a wide range of civil engineering applications, and the same has undergone significant development over the last decade. In this paper, it is demonstrated how a BOCDA-based strain sensor can be employed to monitor cracks in concrete. Crack monitoring on the surface of the concrete member provides useful information for evaluating stiffness and durability of the structure, particularly for early detection of tiny cracks, which is essential for preventing crack growth and dispersion. The crack-induced strain distribution was analytically investigated, and it was proved that BOCDA can identify even a small crack before its visual recognition by a beam test. Moreover, periodical crack monitoring was successfully executed on a pedestrian deck for five years.

The measurement uncertainty of illuminance and, consequently, luminous flux and luminous efficacy of LED lamps can be reduced with a recently introduced method based on the predictable quantum efficient detector (PQED). One of the most critical factors affecting the measurement uncertainty with the PQED method is the determination of the aperture area. This paper describes an upgrade to an optical method for direct determination of aperture area where superposition of equally spaced Gaussian laser beams is used to form a uniform irradiance distribution. In practice, this is accomplished by scanning the aperture in front of an intensity-stabilized laser beam. In the upgraded method, the aperture is attached to the PQED and the whole package is transversely scanned relative to the laser beam. This has the benefit of having identical geometry in the laser scanning of the aperture area and in the actual photometric measurement. Further, the aperture and detector assembly does not have to be dismantled for the aperture calibration. However, due to small acceptance angle of the PQED, differences between the diffraction effects of an overfilling plane wave and of a combination of Gaussian laser beams at the circular aperture need to be taken into account. A numerical calculation method for studying these effects is discussed in this paper. The calculation utilizes the Rayleigh-Sommerfeld diffraction integral, which is applied to the geometry of the PQED and the aperture. Calculation results for various aperture diameters and two different aperture-to-detector distances are presented.

Pavement roughness is one of the most important factors for appraising highway construction. In this paper, we choose the laser triangulation to measure pavement roughness. The principle and configuration of laser triangulation are introduced. Based on this technology, the pavement roughness of a road surface is measured. The measurement results are given in this paper. The measurement range of this system is 50 μm. The measurement error of this technology is analyzed. This technology has an important significance to appraise the quality of highway after completion of the workload.

Heterogeneous networks (HetNets) have the potential to cater for the capacity requirements of mobile broadband services at reduced cost and energy consumption levels. One key aspect in HetNets is the role of the backhaul. More specifically, it is crucial for a mobile operator to understand the impact of specific technological and architectural upgrades in the mobile backhaul network on the capital and operational expenditure (i.e., CAPEX and OPEX). This paper proposes a comprehensive methodology that can be used to analyze the total cost of ownership of a number of backhaul options based on fiber, microwave, and copper technologies. The study considers both a Greenfield and a Brownfield scenario and takes into account the mobile broadband capacity requirements for the time period between years 2015 and 2025. From the results presented in the paper it can be concluded that even though microwave and fiber will be predominately used in the future, the possible migration paths leading to such fiber- and microwave-based backhaul scenarios might be different, depending upon factors such as spectrum and license costs, time to deployment, availability of equipment, and required quality of service levels.

This paper explores the capability of the “surface-protected etching” process for the creation of rattle-type SiO2@void@SiO2 colloidal structures featuring a mesoporous silica shell and a mesoporous movable silica core. The surface-protected etching process involves stabilization of the particle surface using a polymer ligand, and then selective etching of the interior to form hollow structures. In this paper, this strategy has been extended to the formation of rattle-like structures by etching SiO2@SiO2 core shell particles which are synthesized by a two-step sol gel process. The key is to introduce a protecting polymer of polyvinylpyrrolidone (PVP) to the surface of both core and shell in order to tailor their relative stability against chemical etching. Upon reacting with NaOH, the outer layer silica becomes a hollow shell as only the surface layer is protected by PVP and the interior is removed, while the core remains its original size thanks to the protection of PVP on its surface. This process can be carried out at room temperature without the need of additional templates or complicated heterogeneous coating procedures. The etching process also results in the rattle-type colloids having mesoscale pores with two distinct average sizes. In our demonstration of a model drug delivery process, such mesoporous structures show an interesting two-step elution profile which is believed to be related to the unique porous rattle structures.