Quasi-persistent photocurrent in the UV-irradiated MEH-PPV conjugated polymer

We report the quasi-persistent photocurrent in the MEH-PPV conjugated polymer, induced by UV-irradiation in air. It is attributed to the irradiation-induced defects, which also act to accelerate its decay.     

Preparation and characterization of copper(II) tetrasulfonated phthalocyanine nanoparticles formed by laser ablation in poor solvents

Laser irradiation of copper(II) tetrasulfonated phthalocyanine (CuTsPc) microcrystals in poor organic solvents such as methanol, 2-methyl-2-propanol, ethanol, tetrahydrofuran, and acetone has produced CuTsPc nanoparticles with 15–112 nm in diameter. Field emission scanning electron microscopy (FESEM) images have shown the formation of CuTsPc nanoparticles in poor organic solvents used in this work. The mean diameters of CuTsPc nanoparticles obtained from transmission electron microscopy (TEM) images in methanol, 2-methyl-2-propanol, ethanol, tetrahydrofuran, and acetone were determined to be 26, 36, 35, 86, and 78 nm, respectively. A correlation between the size of CuTsPc nanoparticles and a solvent polarity could be found in this work.     

Synthesis and spectroscopic investigation of π‐conjugated (E)‐enyne polycarbazole with different organo‐metallic catalysts from 3,6‐diethynyl‐9‐(2‐ethylhexyl)carbazole

In the present study, a new (E)‐rich‐enyne π‐conjugated polymer containing a carbazole was designed and synthesized. Two different synthesis methods of poly[N‐(2‐ethylhexyl)‐3,6‐carbazolyleneethynylene‐(E)‐vinylene] (PCZEV) have been prepared from 3,6‐diethynyl‐9(2‐ethylhexyl)carbazole by using the palladium‐carbene‐catalyzed reaction and/or by using the organolanthanide‐catalyzed reaction leading to well‐defined polymer, and their general properties were studied. Compared to poly[N‐(2‐ethylhexyl)‐3,6‐carbazolyleneethynylene] (PCE), the UV‐vis absorption and photoluminescence of the PCZEV was red‐shifted, which indicates the extension of conjugation length. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2434–2442, 2009     

Quantitative small-angle light-scattering studies of the melting and crystallization of LLDPE/LDPE blends

Small-angle light-scattering (SALS) patterns were obtained during melting and crystallization of blends of linear low-density polyethylene (LLDPE) with conventional low-density polyethylene (LDPE). Quantitative measurements of these SALS patterns using a two-dimensional optical multichannel analyzer apparatus (OMA2) indicate that the LLDPE which is miscible with the LDPE component in the molten state crystallizes first, forming volume-filling spherulites. The LDPE then crystallizes within the preformed spherulites. These findings are supported by optical microscopy studies showing that the blend samples were volume filled with one kind of the spherulites having a radius comparable to that of the pure LLDPE. The SALS intensity curve changes with composition of the blends in a manner that may be interpreted by considering the orientation of crystals within spherulites. It has been observed that the spherulites in the blend have more diffuse boundaries as the LDPE content increases. The lattice spacing and long spacings in blends were obtained by wide-angle and small-angle x-ray scattering, respectively. The SALS technique along with differential scanning calorimetry (DSC) is shown to be useful for determining the crystallization behavior of a crystallizable polymer blend system.     

Experimental investigation of combustion instabilities of a mesoscale multinozzle array in a lean-premixed combustor

Self-excited combustion instabilities in a mesoscale multinozzle array, also referred to as a micromixer-type injector, have been experimentally investigated in a lean-premixed tunable combustor operating with preheated methane and air. The injector assembly consists of sixty identical swirl injectors of 6.5 mm inner diameter, which are evenly distributed across the combustor dump plane. Their flow paths are divided into two groups – inner and outer stages – to form radially stratified reactant stoichiometry for the control of self-excited instabilities. OH PLIF measurements of stable flames reveal that the presence of radial staging has a remarkable influence on stabilization mechanisms, reactant jet penetration/merging, and interactions between adjacent flame fronts. In an inner enrichment case, two outer (leaner) streams merge into a single jet structure, whereas the inner (richer) reactant jets penetrate far downstream without noticeable interactions between neighboring flames. The constructed stability map in the 〈?_i, ?_o〉 domain indicates that strong self-excited instabilities occur under even split and outer enrichment conditions at relatively high global equivalence ratios. This is attributed to large-scale flame surface deformation in the streamwise direction, as manifested by vigorous detachment/attachment movements. The use of the inner fuel staging method was found, however, to limit the growth of large-amplitude heat release rate fluctuations, because the center flames are securely anchored during the whole period of oscillation, giving rise to a moderate lateral motion. We demonstrate that the collective motion of sixty flames – rather than the individual local flame dynamics – play a central role in the development of limit cycle oscillations. This suggests that the distribution pattern of the injector array, in combination with the radial fuel staging scheme, is the key to the control of the instabilities.     

Direct comparison of self-excited instabilities in mesoscale multinozzle flames and conventional large-scale swirl-stabilized flames

The present experimental investigation demonstrates important trends and offers physical insights into self-excited combustion instabilities in mesoscale multinozzle flames composed of sixty small injectors. Here we focus on the response of a prototypical micromixer-type injector assembly, fabricated using an additive manufacturing technique, in comparison with the behavior of conventional large-scale swirl-stabilized flames. Our results highlight that the development of self-excited instabilities in unconventional mesoscale flames is fundamentally different from that in large-scale swirl flames, in terms of the onset of instabilities, nonlinear modal dynamics, and amplitude/frequency of limit cycle oscillations under the same operating conditions. These differences are attributable to the alteration in local flow/flame structures and the resulting flame-to-flame/flame-wall interaction mechanisms. An integrated analysis of large datasets reveals that the two interacting swirl-stabilized flames tend to couple strongly with a low-frequency L1 mode at about 220 Hz, whereas the sixty-injector small-scale flames are capable of triggering multiple higher-frequency instabilities at ～ 310, ～ 470, and ～ 600 Hz. That is, the use of the micromixer-type injector assembly in a lean-premixed system causes the occurrence of combustion instabilities to shift toward a higher equivalence ratio. However, due to the absence of a large recirculation zone near the primary reaction region, the combustion system equipped with the small-scale multinozzle injectors was found to suffer from lean blowoff phenomena at low equivalence ratio.     

Detection of mutant p53 using field-effect transistor biosensor

We assessed the abilities of wild p53 and mutant p53 proteins to interact with the consensus DNA-binding sequence using a MOSFET biosensor. This is the first report in which mutant p53 has been detected on the basis of DNA-protein interaction using a FET-type biosensor. In an effort to evaluate the performance of this protocol, we constructed the core domain of wild p53 and mutant p53 (R248W), which is DNA-binding-defective. After the immobilization of the cognate DNA to the sensing layer, wild p53 and mutant p53 were applied to the DNA-coated gate surface, and subsequently analyzed using a semiconductor analyzer. As a consequence, a significant up-shift in drain current was noted in response to wild p53, but not mutant p53, thereby indicating that sequence-specific DNA-protein interactions could be successfully monitored using a field-effect-based biosensor. These data also corresponded to the results obtained using surface plasmon resonance (SPR) measurements. Taken together, our results show that a FET-type biosensor might be promising for the monitoring of mutant p53 on the basis of its DNA-binding activity, providing us with very valuable insights into the monitoring for diseases, particularly those associated with DNA-protein binding events.     

Mesoporous Nickel–Alumina Catalysts for Hydrogen Production by Steam Reforming of Liquefied Natural Gas (LNG)

Recent progress on the mesoporous nickel–alumina catalysts for hydrogen production by steam reforming of liquefied natural gas (LNG) was reported in this review. A number of mesoporous nickel–alumina composite catalysts were prepared by a single-step surfactant-templating method using cationic, anionic, and non-ionic surfactant as structure-directing agents for use in hydrogen production by steam reforming of LNG. For comparison, nickel catalysts supported on mesoporous aluminas were also prepared by an impregnation method. The effect of preparation method and surfactant identity on physicochemical properties and catalytic activities of mesoporous nickel–alumina catalysts in the steam reforming of LNG was investigated. Regardless of preparation method and surfactant identity, nickel oxide species were finely dispersed on the surface of mesoporous nickel–alumina catalysts through the formation of surface nickel aluminate phase. However, nickel dispersion and nickel surface area of mesoporous nickel–alumina catalysts were strongly affected by the preparation method and surfactant identity. It was found that nickel surface area of mesoporous nickel–alumina catalyst served as one of the important factors determining the catalytic performance in hydrogen production by steam reforming of LNG. Among the catalysts tested, a mesoporous nickel–alumina composite catalyst prepared by a single-step non-ionic surfactant-templating method exhibited the best catalytic performance due to its highest nickel surface area.