Titanium is used as a metal for biocompatible materials such as dental implants or restorations because of its excellent chemical stability. However, the corrosion of Ti in the prophylactic fluoride-containing environment can become problematic. To clarify the effects of fluoride concentration and pH on the corrosion behavior of Ti, we conducted anodic polarization and immersion tests in NaF solution of various concentrations and pH values. The concentrations of dissolved Ti in the test solutions were analyzed by inductively coupled plasma mass spectroscopy. There were obvious limits of fluoride concentration and the pH value at which the corrosion behavior of Ti changed. The corrosion of Ti in the solution containing fluoride depended on the concentration of hydrofluoric acid (HF). When the HF concentration in the solution was higher than about 30 ppm, the passivation film of the Ti was destroyed. The results of this study revealed a relation between the fluoride concentrations and pH values at which Ti corrosion occurred and provided data on such corrosion in environments where the fluoride concentration and pH value are known.
Single-walled carbon nanotubes (SWNTs) show unique photoluminescence (PL) in the near-infrared (NIR) region. Here we propose a concept based on the proximal modification in local covalent functionalization of SWNTs. Quantum mechanical simulations reveal that the SWNT band gap changes specifically based on the proximal doped-site design. Thus, we synthesize newly-designed bisdiazonium molecules and conduct local fucntionalisation of SWNTs. Consequently, new red-shifted PL (E112*) from the bisdiazonium-modified SWNTs with (6, 5) chirality is recognized around 1250 nm with over ~270 nm Stokes shift from the PL of the pristine SWNTs and the PL wavelengths are shifted depending on the methylene spacer lengths of the modifiers. The present study revealed that SWNT PL modulation is enable by close-proximity-local covalent modification, which is highly important for fundamental understanding of intrinsic SWNT PL properties as well as exciton engineering–based applications including photonic devices and (bio)imaging/sensing.
We present a concept to modulate near infrared photoluminescence (NIR-PL) from locally-functionalized single-walled carbon nanotubes (local-f-SWNTs) based on a molecular recognition approach using newly synthesized phenylboronic acid (PB)-functionalized local-f-SWNTs (PB-SWNTs) and saccharides, in which a selective PL spectral shift is observed by addition of the saccharides.
Final oocyte maturation and ovulation of captive chub mackerel Scomber japonicus with fully yolk-accumulated oocytes were induced by a single injection of human chorionic gonadotropin. Reproductive parameters, including spawning frequency and batch fecundity, which are required to estimate spawning biomass in pelagic fish by the daily egg production method, were analyzed. Germinal vesicle migration (GVM) occurred at 18-24 h post-injection, and the hydration and ovulation of oocytes were completed at 30 and 36 h post-injection, respectively. The results of the maturation process suggest that fish with GVM-stage ovaries captured in the daytime from the field are capable of spawning on the night following their capture. The oocytes used in the oocyte sizefrequency distribution method for batch fecundity estimates should be at late GVM and more advanced stages. The results of sequential artificial insemination showed that the quality of ovulated eggs held in the ovarian lumen rapidly deteriorated as time progressed after ovulation. This indicates that the fertilization window for the ovulated eggs of chub mackerel lasts only a few hours, and spawning behavior should be performed within a few hours after ovulation in the wild population.KEY WORDS: batch fecundity, chub mackerel, fertilization rate, final oocyte maturation, human chorionic gonadotropin, ovulation.
The doped sites of locally functionalized single-walled carbon nanotubes show unique solvatochromic behaviors in their near-infrared photoluminescence.
We newly introduce positional isomeric structures at the defect sites of locally-functionalized single-walled carbon nanotubes (lf-SWNTs) showing unique near infrared photoluminescence (PL). The observed PL is significantly different from that of typical para-aryl modified lf-SWNTs; i.e., (i) an extraordinary PL wavelength shift of the meta-aryl modified lf-SWNTs, and (ii) remarkably red-shifted PL from the ortho-aryl modified lf-SWNTs are revealed.
Single-walled carbon nanotubes (SWNTs) with local chemical modification have been recognized as a novel near infrared (NIR) photoluminescent nanomaterial due to the emergence of a new red-shifted photoluminescence (PL) with enhanced quantum yields. As a characteristic feature of the locally functionalized SWNTs (lf-SWNTs), PL wavelength changes occur with the structural dependence of the substituent structures in the modified aryl groups, showing up to a 60 nm peak shift according to an electronic property difference of the aryl groups. Up to now, however, the structural effect on the electronic states of the lf-SWNTs has been discussed only on the basis of theoretical calculations due to the very limited amount of modifications. Herein, we describe the successfully-determined electronic states of the aryl-modified lf-SWNTs with different substituents (Ar-X SWNTs) using an in situ PL spectroelectrochemical method based on electrochemical quenching of the PL intensities analyzed by the Nernst equation. In particular, we reveal that the local functionalization of (6,5)SWNTs induced potential changes in the energy levels of the HOMO and the LUMO by -23 to -38 meV and +20 to +22 meV, respectively, compared to those of the pristine SWNTs, which generates exciton trapping sites with narrower band gaps. Moreover, the HOMO levels of the Ar-X SWNTs specifically shift in a negative potential direction by 15 meV according to an enhancement of the electron-accepting property of the substituents in the aryl groups that corresponds to an increase in the Hammet substituent constants, suggesting the importance of the dipole effect from the aryl groups on the lf-SWNTs to the level shift of the frontier orbitals. Our method is a promising way to characterize the electronic features of the lf-SWNTs.
Single-walled carbon nanotubes doped with a limited amount of oxygen (O-doped SWNTs) are expected to be novel materials due to the appearance of red-shifted new emission and enhancement of the luminescence quantum yields compared to those of pristine SWNTs, which are of importance for the development of high performance biosensors, imaging materials, and optical devices. The appearance of the new optical properties is due to the change in the electronic states induced by the oxygen doping (Odoping) of the SWNTs, thus quantitative analysis of the electronic states of the O-doped SWNTs is crucial. In this study, we have successfully determined the precise electronic states of the O-doped SWNTs based on the in situ photoluminescence (PL) electrochemical method. The measurements revealed the presence of at least two distinct O-doping sites with unique optical and electrochemical properties for all four studied chiralities. The electrochemical measurements also showed that shifts in the valence and conduction band resulting from the O doping are on the order of 0.02−0.03 eV, which is much lower than the red shift of the photoluminescence peak. This behavior agrees with the theoretical simulations using the density functional based tight binding (DFTB) method. This study suggests that the doped sites on the SWNTs act as a neutral quantum dot trapping exciton generated on the tubes.
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