Influence of grain boundary connectivity on the trapped magnetic flux of multi-seeded bulk superconductors

The top-seeded melt-growth process with multi-seeding technique provides a promising way to fabricate large-sized bulk superconductors in an economical way. To understand the essential characteristics of the multi-seeded bulks, the paper reports the influence of the grain boundary (GB) coupling or connectivity on the total trapped magnetic flux. The coupling ratio, the lowest trapped flux density in the GB area to the averaged top value of the two neighboring peak trapped fields, is introduced to reflect the coupling quality of GBs inside a multi-seeded bulk. By the trapped flux density measurement of four different performance multi-seeded YBCO bulk samples as representatives, it was found that the GB coupling plays an important role for the improvement of the total trapped magnetic flux; moreover, somewhat more significant than the widely used parameter of the peak trapped fields to evaluate the physical performance of bulk samples. This characteristic is different with the case of the well-grown single-grain bulks.     

Living cationic polymerization of a coumarin‐substituted vinyl ether and reversible photoinduced crosslinking of the resulting homopolymers and amphiphilic block copolymers

Living cationic polymerization of 4‐methyl‐7‐(2‐vinyloxyethoxy)coumarin (CMVE) was achieved using SnCl₄ in the presence of nBu₄NBr as an added salt at 0 °C. The number‐average molecular weight of the resulting polymers increased in direct proportion to the monomer conversion while retaining relatively low polydispersity. Structural analysis revealed that the resulting polymers carried pendant coumarinyl moieties. These coumarinyl moieties were crosslinked by irradiation with UV light at λ_max = 366 nm, and the crosslinked sites were then cleaved by irradiation with UV light at λ_max = 254 nm. The crosslinking behaviors of the polymers were studied by UV and FTIR spectroscopic measurement. PolyCMVE was soluble in dichloromethane but was found to be insoluble upon UV light irradiation. We also synthesized amphiphilic block polymers bearing coumarinyl moieties by living cationic copolymerization with an amphiphilic vinyl ether. The resulting block polymers were soluble in an aqueous medium and also formed micelle‐like aggregates. Upon UV irradiation of aqueous solutions above the critical micelle concentration, an efficient crosslinking reaction occurred. Photoinduced structural changes of these polymer aggregates in the solution state were further investigated. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

A time-resolved fluorescence probe for dipeptidyl peptidase 4 and its application in inhibitor screening

The prevalence of type 2 diabetes is increasing dramatically throughout the world. Recently, dipeptidyl peptidase 4 (DPP4) was identified as a potential antidiabetes target. Many DPP4 inhibitors, such as sitagliptin and vildagliptin, have been developed and marketed, but superior therapeutic agents are still required. Therefore, we have developed new methodology for screening of DPP4 inhibitors. Absorption-based measurements with para-nitroaniline or fluorescence-based measurements with the coumarin derivative 7-amino-4-methylcoumarin are often used for the screening of protease inhibitors, including DPP4 inhibitors, but these strategies are not sufficiently sensitive because of interfering background absorption and fluorescence, thus giving rise to many false-positive and false-negative results. Therefore, we have designed and synthesised a novel DPP4 probe (Gly-Pro-BCD-Tb; Gly=glycine, Pro=proline, andBCD defines the backbone of the probe comprising an aniline derivative as on/off switch, a 7-amino-4-methyl-2(1H)-quinolinone (cs-124) as antenna moiety, and a diethylenetriamine-N,N,N',N',N'-pentaacetic acid (DTPA) as chelator moiety, Tb=terbium) for time-resolved fluorescence (TRF) measurements. TRF measurements with Gly-Pro-BCD-Tb showed high sensitivity and reliability in the inhibitory assay relative to Gly-Pro-MCA (MCA=4-methylcoumarin-7-amide), a conventional fluorescence probe for DPP4. Further, we employed our probe for high-throughput DPP4 inhibitor screening with 3841 randomly selected compounds and found that epibestatin, an epimer of bestatin (a well-known anticancer drug and general aminopeptidase inhibitor), showed dose-dependent DPP4 inhibitory activity. Interestingly, bestatin did not exhibit DPP4 inhibitory activity. We believe that this screening system will be useful for the discovery of DPP4 inhibitors with novel structural scaffolds.     

Influence of nonlinear atomic interaction on excitation of intrinsic localized modes in carbon nanotubes

Excitation of intrinsic localized modes (ILMs) in carbon nanotubes (CNTs) with different chiral structures was investigated by molecular dynamics simulations. For CNTs with a chiral angle less than or equal to 30^°, energy concentration that continued for more than 200 fs was found in a localized area, where a pair of neighboring atoms strongly oscillated with a higher vibrational frequency than the upper bound of phonon bands. This evidently indicates excitation of the ILM. On the other hand, the ILM was not excited in CNTs with a chiral angle greater than or equal to 41^°. Analyzing the nonlinearity of the interaction between excited atoms in the ILM vibration mode, we elucidated that nonlinearity predominates the selective ILM excitation. Furthermore, stronger nonlinearity excites ILMs with both higher frequency and longer lifetime.     

Spatial variation of superconducting properties of Gd123 Bulk superconductors with magnetic particles addition

Magnetic flux trapping and the homogeneity of the flux pinning are essential problems in the practical application of high-temperature superconductors. We have conducted study on the role of addition of soft magnetic Fe-B alloy particles contribute to the enhancement of the critical current density (J_c) under wide-range of magnetic field. Magnetic flux trapping was enhanced in Gd123 bulk superconductor with suitable amount of magnetic particles addition. In addition, it can be effective as pinning center enhance the J_c of the bulk in both the a–b growth sector and the c-growth sector under magnetic field. However, the T_c of the Gd123 bulk was decreased obviously by addition of magnetic particles. The study on the spatial variation of superconducting properties indicates that the performance of the upper part of the bulk is better than the bottom. By comparing the superconducting properties of the Gd123 bulk with magnetic particles addition and without magnetic particles addition, we concluded that there is a trace of the formation of homogeneous pinning properties in the magnetic particles addition Gd123 bulk.     

Enhancement of critical current density in Gd123 bulk superconductor doped with magnetic powder

We studied the materials processing to grow high performance magnet with doping of magnetic powder as candidature of pinning centers. The magnetic powder was doped into Gd123 matrix and grew into single domain bulk in air. With doping magnetic powder in Gd123 bulk superconductors, the flux pinning was enhanced and the underlying mechanism was discussed. The experimental results showed that suitable amount of magnetic powder inclusion can be effect as pinning center to enhance the J_c of the bulk both in low magnetic field and high magnetic field, which was different from the bulk doped with paramagnetic nano-scaled particles. The T_c of the bulk was suppressed obviously with the content of the magnetic powder increasing, form 93.0 K without doping decrease to 90.5 K with 0.12 wt.% doping. This is consistent with that the magnetic impurities generally suppress superconductivity. We report the detailed results from the viewpoint of practical application to increase the integrated flux trapped inside the bulk.     

Precise measurement of the self-diffusion coefficient for poly(ethylene glycol) in aqueous solution using uniform oligomers

Uniform poly(ethylene glycol) (PEG) oligomers, with a degree of polymerization n=1-40, were separated by preparative supercritical fluid chromatography from commercial monodispersed samples. Diffusion coefficients, D, for separated uniform PEG oligomers were measured in dilute solutions of deuterium oxide (D(2)O) at 30 degrees C, using pulsed-field gradient nuclear magnetic resonance. The measured D for each molecular weight was extrapolated to infinite dilution. Diffusion coefficients obtained at infinite dilution follow the scaling behavior of Zimm-type diffusion, even in the lower molecular weight range. Molecular-dynamics simulations for PEG in H(2)O also showed this scaling behavior, and reproduced close hydrodynamic interactions between PEG and water. These findings suggest that diffusion of PEG in water is dominated by hydrodynamic interaction over a wide molecular weight range, including at low molecular weights around 1000.     

Near–Infrared‐Responsive Peptide that Targets Collagen Fibrils to Induce Cytotoxicity

A novel conjugate, PHG10 dye, was synthesized using a collagen peptide and a near–infrared (NIR)‐responsive dye to achieve targeted cytotoxicity. The collagen peptide motif, ‐(Pro‐Hyp‐Gly)₁₀‐ (PHG10), was incorporated for targeting collagen fibrils that are excessively produced by activated fibroblasts around tumor cells. PHG10 dye was purified by HPLC and identified by MALDI‐MS. The phototoxicity and cytotoxicity of PHG10 dye were examined using human glioma cells (HGCs). Fluorescent images indicated that PHG10 dye preferably assembled to collagen‐coated HGCs compared with noncoated HGCs. Under irradiation with NIR light, effective cytotoxicity was observed on collagen‐coated HGCs within 20 min. Because phototoxicity and cytotoxicity are dependent on the assembled amount of PHG10 dye, the targeting of collagen fibrils by the collagen peptide motif PHG10 is assured.     

Active species transfer-type artificial light harvesting system in the nanosheet – Dye complexes: Utilization of longer wavelength region of sunlight

A novel light harvesting system that captures long-wavelength light of sunlight by the use of hole transfer was newly investigated. Ga phthalocyanine(Ga^IIITMAPc⁴⁺(D)) and Ru porphyrin(Ru^IIDMPyMP²⁺(A)) co-adsorbed reaction system on the synthetic nanosheet was examined as an artificial light harvesting system. By irradiating 660?nm light, where Ga^IIITMAPc⁴⁺(D) absorbs, to the system under a presence of PtCl₆^2? as an electron acceptor, cation radical of Ru^IIDMPyMP²⁺(A) was produced despite that Ru porphyrin adsorbs only 413 and 533?nm light. The efficient hole transfer reaction from Ga^IIITMAPc⁴⁺(D)⁺, that is generated from its excited state, to Ru^IIDMPyMP²⁺(A) takes place on the nanosheet.     

Capillary high-performance liquid chromatography/electrospray ion trap time-of-flight mass spectrometry using a novel nanoflow gradient generator

A type of high-performance liquid chromatography (HPLC) based on a novel nanoflow gradient generator (Asymptotic-Trace-10-Port-Valve (AT10PV) nanoGR generator) was developed and coupled with an electrospray ion trap time-of-flight mass spectrometer (ESI-IT-TOF MS). Stability of the nanoflow GR HPLC system was tested at flow rates of 20 and 50 nL/min by using a nanoflow meter. Average flow rates in a 2-h run were 51.2 nL/min with RSD 0.7% and 21.0 nL/min with RSD 1.8%. Repeatability of analysis of the nanoHPLC/ESI-IT-TOF MS system was also tested by injecting 1.0 microL of trypsin digested bovine serum albumin (BSA) (100 fmol) into a monolithic silica-ODS column (30 microm i.d., 150 mm in length) through a packed silica-ODS trapping column (particle size 5 microm, 150 microm i.d., 10 mm in length). At a flow rate of 50 nL/min, the result demonstrated a reasonably good repeatability of peak retention times (RSD: 0.32-1.1%) and base-ion peak areas (RSD: 4.4-6.6%).