Enlightening darkness to diffraction limit and beyond: comparison and optimization of different polarizations for dark spot generation

We compare generation of a dark spot using focusing of beams with azimuthal polarizion, radial polarization with a vortex, and a circular polarization with either a first or second order vortex. By optimization of the amplitude-phase pupil, it is ascertained that azimuthal polarization is the most suitable one to obtain the diffraction bounded dark spot per se whose scalar approximation limit has FWHM=0.29λ. Consequently, for dark spot generation, this polarization plays the role of the radial polarization in creation of the diffraction-limited bright spot. Using azimuthal polarization, it is shown that an amplitude-phase filter allows generation of a subdiffractive dark spot in a prescribed finite area.     

Electronic fingerprints of DNA bases on graphene

We calculate the electronic local density of states (LDOS) of DNA nucleotide bases (A,C,G,T), deposited on graphene. We observe significant base-dependent features in the LDOS in an energy range within a few electronvolts of the Fermi level. These features can serve as electronic fingerprints for the identification of individual bases in scanning tunneling spectroscopy (STS) experiments that perform image and site dependent spectroscopy on biomolecules. Thus the fingerprints of DNA-graphene hybrid structures may provide an alternative route to DNA sequencing using STS.     

Generating inhomogeneously polarized higher-order laser beams by use of diffractive optical elements

We propose an improved version of the earlier developed optical arrangement for generating inhomogeneously polarized laser light modes with the aid of a diffractive optical element (DOE) with carrier frequency. By eliminating lenses from the optical arrangement, we achieve the miniaturization, reduced light losses, a smaller number of parameters being matched, and a simpler system adjustment procedure. Note that all the capabilities of the previous version, namely, the universality and simple readjustment to different polarization types, are fully retained. The numerical modeling of the polarization mode combiner has made it possible to analyze its performance and capabilities. In the experiments, the quality of the resulting beams is shown to be improved. For generating higher-order cylindrical beams, a lower-order mode at the output of the polarization mode combiner is additionally transformed with a DOE that operates in the zero diffraction order, introducing radial phase changes.     

Light‐Controlled Reversible Manipulation of Microgel Particle Size Using Azobenzene‐Containing Surfactant

The light‐induced reversible switching of the swelling of microgel particles triggered by photo‐isomerization and binding/unbinding of a photosensitive azobenzene‐containing surfactant is reported. The interactions between the microgel (N‐isopropylacrylamide, co‐monomer: allyl acetic acid, crosslinker: N,N′‐methylenebisacrylamide) and the surfactant are studied by UV‐Vis spectroscopy, dynamic and electrophoretic light scattering measurements. Addition of the surfactant above a critical concentration leads to contraction/collapse of the microgel. UV light irradiation results in trans‐cis isomerization of the azobenzene unit incorporated into the surfactant tail and causes an unbinding of the more hydrophilic cis isomer from the microgel and its reversible swelling. The reversible contraction can be realized by blue light irradiation that transfers the surfactant back to the more hydrophobic trans conformation, in which it binds to the microgel. The phase diagram of the surfactant‐microgel interaction and transitions (aggregation, contraction, and precipitation) is constructed and allows prediction of changes in the system when the concentration of one or both components is varied. Remote and reversible switching between different states can be realized by either UV or visible light irradiation.     

P3HT/PCBM Bulk Heterojunction Solar Cells: Impact of Blend Composition and 3D Morphology on Device Performance

The performance of polymer solar cells (PSC) strongly depends on the 3D morphological organization of the donor and acceptor compounds within the bulk heterojunction active layer. The technique of electron tomography is a powerful tool for studying 3D morphology of the layers composed of poly(3‐hexylthiophene) (P3HT) and a fullerene derivative ([6,6]‐phenyl‐C61‐butyric acid methyl ester; PCBM), especially to quantify the amount and distribution of fibrillar P3HT nanocrystals throughout the volume of the active layer. In this study, electron tomography is used to characterize P3HT/PCBM layers with different blend compositions, both before and after thermal annealing. The power conversion efficiency of the corresponding PSCs is strongly dependent on the overall crystallinity of P3HT and the way P3HT crystals are distributed throughout the thickness of the active layer.     

Technology transfer projects in developing countries—furthering the Project Management perspectives

This paper attempts to broaden the analysis of the technology transfer phenomenon by refocusing research attention on the level of performance assessment of technology transfer projects. An holistic evaluation framework based on the considerations of an extended Project Life Cycle model is proposed to overcome some of the shortcomings of conventional approaches to project evaluation. This also reinforces the need for open systems thinking in assessing and managing risk of technology transfer projects. The discussion is based on two case studies which articulate the experiences with two integrated mechanisms of technology transfer used in Algeria from 1965 to 1990: turnkey and “product-in-hand”. The aim is to gain a better understanding of the processes of technology transfer and to contribute to the improvement of associated managerial practices in developing economies.     

Purification of brines by chemical precipitation and ion‐exchange processes for obtaining battery‐grade lithium compounds

Lithium salts are very important in the production of lithium batteries since they are used as precursors for the fabrication of cathode materials that require very low level of impurities (battery grade). Usually, the lithium extraction process from brine first yields lithium carbonate, which is then used as raw material for the production of other lithium compounds. However, it implies an increase in investment costs, considering more equipment and process stages. To remove the impurities and produce battery‐grade lithium compounds directly from brines, a laboratory‐scale process was developed using the methods of ion exchange and chemical precipitation. Thus, impurity‐free brine ready to be used in an industrial membrane electrolysis process is obtained. Different sequences and operating conditions were investigated for the purification of lithium‐concentrated brines, removing the main impurities of the natural brines: calcium, magnesium, and sulfate. For the characterization of solutions, crystals, and ion‐exchange resins, atomic absorption spectrophotometry, scanning electron microscopy, and X‐ray scattering spectroscopy were used. The results indicate that during the chemical precipitation process, lithium‐concentrated brine reacted with some additives (precipitating agents) at different stages in the batch reactors. Subsequently, the pulp obtained was sedimented and filtered, eliminating or reducing the impurities of the lithium brine. Thus, the most efficient precipitation sequence was evaluated as a function of the removal percentage of the species. The removal efficiencies obtained for Ca⁺², Mg⁺², and SO₄^?2 were of 98.93%, 99.93%, and 97.14%, respectively. Thereafter, the use of the ion‐exchange resins reduced the concentration of Ca⁺² and Mg⁺² to the values below 1 ppm. The combined use of both processes provided promising results that could be applied in the industry.     

Distribution of vanadium and vanadyl porphyrins during fractionation of resins of heavy sulfurous oils

Features of the content and distribution of vanadium and vanadyl porphyrins in the fractions of resins, which were obtained by separation using column chromatography on silica, have been studied on heavy sulfurous oils of various deposits of the Volga–Ural basin (Russia). The difference of the vanadium and vanadyl porphyrin contents in the fractions of oils of various production complexes has been shown. Features of structural–group composition and predominant types of vanadyl porphyrins in the fractions of resins have been determined.     

Non-linear unit root properties of crude oil production

While there is good reason to expect crude oil production to be non-linear, previous studies that have examined the stochastic properties of crude oil production have assumed that crude oil production follows a linear process. If crude oil production is a non-linear process, conventional unit root tests, which assume linear and systematic adjustment, could interpret departure from linearity as permanent stochastic disturbances. The objective of this paper is to test for non-linearities and unit roots in crude oil production. To realize our objective, this study applies a threshold autoregressive model with an autoregressive unit root to monthly crude oil production for 17 OPEC and non-OPEC countries over the period January 1973 to December 2007. Specifically, first we test for the presence of non-linearities (threshold effects) in the production of crude oil in two regimes. Second, we test for a unit root against a non-linear stationary process in two regimes and a partial unit root process when the unit root is present in one regime only. We find that crude oil production is characterized by threshold effects. We find that for eleven of the countries a unit root was present in both regimes, while for the others a partial unit root was found to be present in either the first regime or second regime.     

Adsorption of methyl mercaptan on activated carbons

Activated carbons of different origins were studied as methyl mercaptan adsorbents in wet, dry, and oxidizing conditions. The materials were characterized using adsorption of nitrogen, Boehm titration, and thermal analysis. Investigation was focused on the feasibility of the removal of methyl mercaptan on activated carbons and on the role of surface chemistry and porosity in the adsorption/oxidation processes. The results showed relatively high capacities of carbons for removal of CH3SH. The amount adsorbed depends on the surface features. Methyl mercaptan, in general, is oxidized to disulfides, which, depending on the chemistry of the carbon surface, can be converted to sulfonic acid due to the presence of water and active radicals.