Gaze direction modulates the disengagement of attention from facial expression in 10-month-olds.

This study investigated whether the disengagement of attention from facial expression is modulated by gaze direction in infants. To this end, we measured the saccadic reaction time required for the 10-month-olds to disengage their attention from angry and happy expressions combined with either straight or averted gaze. The 10-month-olds' disengagement of their attention from happy faces was modulated by gaze direction. This finding indicates that gaze direction strongly influences infants' allocation of attention to facial expressions. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Electrochemical insertion and extraction of lithium-ion at nano-sized LiMn2O4 particles prepared by a spray pyrolysis method

Nano-sized LiMn₂O₄ particles were prepared at 1023 K by electrospray pyrolysis in which they were directly deposited on a Pt substrate in gas phase. Cyclic voltammetry gave very sharp and symmetrical redox peaks at ca. 4.0 and 4.1 V vs. Li/Li⁺ owing to the insertion and extraction of lithium-ion at LiMn₂O₄. However, the redox peaks broadened and their peak separation in an electrode potential increased when aggregated nano-sized LiMn₂O₄ particles were used. In Nyquist plots, a semi-circle due to lithium-ion transfer resistance appeared at potentials above 3.90 V. The values of the lithium-ion transfer resistances were small for dispersed nano-sized LiMn₂O₄ particles. On the other hand, the lithium-ion transfer resistances increased and the Warburg impedance became obvious as the nano-sized LiMn₂O₄ particles aggregated. These results clearly indicate that the apparent rapid diffusion of lithium-ion can be attained using well-dispersed nano-sized particles of electroactive materials.     

Preparation and electrochemical properties of SiO2–non-graphitizable carbon composites as negative electrode materials for Li-ion batteries

SiO₂–non-graphitizable carbon composites were prepared by pyrolysis of a mixture of ethyl cellulose and nano-sized SiO₂. The composite electrode showed high reversibility in insertion and/or extraction reactions of Li ions at potentials below 1 V with little hysteresis after the 2nd cycle, whereas a large irreversible capacity was observed in the 1st cycle. This reversible capacity increased with increasing SiO₂ content above 5 wt%. Li ion transfer at the interface between a composite electrode and an electrolyte was studied by ac impedance spectroscopy. In the Nyquist plots, a semi-circle that was assigned to charge-transfer resistance (R _ct) because of Li ion transfer across the interface between the composite electrode and electrolyte appeared at potentials below 1 V. The values of R _ct decreased with increasing SiO₂ content. These results indicate that both a decrease in R _ct and an increase in reversible capacity can be achieved by use of SiO₂–non-graphitizable carbon composite electrodes; this would lead to Li-ion batteries with higher power and energy density.     

Living activity recognition using off-the-shelf sensors on mobile phones

In aging societies, such as that of Japan, there is growing awareness that robotic technology has the potential to help both physical and mental labor. To take an example of mental labor, the robotic technology can contribute as an interface to home electric appliances and a conversation partner with interactive communication. In this case, it is important to recognize the elderly user’s activities for not only watching-over services but also improving the quality of the conversation. We propose a low-throughput recognition method for in-home living activity recognition using only off-the-shelf sensors, namely an accelerometer and a microphone, which are commonly applied in mobile phones. The system can determine whether the user is walking, quiet, or performing a task by acceleration sensing, and then in the latter case, acoustic sensing can be used to classify the nature of the task that the user is performing. We conducted two experiments to confirm the feasibility of the proposed method. As a result of the first experiment, three movement conditions are classified with more than 95?% accuracy by acceleration sensing: walking, quiet, or performing a task. And it classified the nature of the task into brushing teeth, shaving, drying the hair with a hairdryer, flushing the toilet, vacuuming, washing the dishes, and ironing with 75.8?% accuracy by acoustic sensing and improved the accuracy to 85.9?% by training with only the subject’s own data. Moreover, the result of the second experiment shows that it is effective to adopt instance-based recognition which is an additional recognition scheme per each continuous task, according to the assumed application.     

Magnetite nanoparticles with high heating efficiencies for application in the hyperthermia of cancer

Magnetic hyperthermia is a safe method for cancer therapy. A gap-type alternating current magnetic field (100 kHz, 100–300 Oe) is expected to be clinically applicable for magnetic hyperthermia. In this study, magnetite nanoparticles (MNPs) varying in size from 8 to 413 nm were synthesized using a chemical coprecipitation and an oxidation precipitation method to find the optimum particle size that shows a high heating efficiency in an applied magnetic field. The particles' in vitro heating efficiency in an agar phantom at an MNP concentration of 58 mg Fe/ml was measured in an applied magnetic field. In a magnetic field of 120 Oe, the temperature increase (ΔT) of the agar phantom within 30 s was 9.3 °C for MNPs with a size of 8 nm, but was less for the other samples, while in a magnetic field of 300 Oe, ΔT = 55 °C for MNPs with a size of 24 nm, and ΔT = 25 °C for MNPs with a size of 8 nm. The excellent heating efficiency of MNPs with a size of 24 nm in a magnetic field of 300 Oe may be due to a combination of the effects of both relaxation and hysteresis losses of the magnetic particles. It is believed that MNPs with a size of 8–24 nm will be useful for the in situ hyperthermia treatment of cancer.     

Effects of oxygen content of porous titanium metal on its apatite-forming ability and compressive strength

Porous titanium metal subjected to NaOH and heat treatments is useful as a bone substitute as it shows high mechanical strength as well as osteoconductivity and osteoinductivity. However, the porous metal is liable to be contaminated with oxygen gas during the fabrication process and this incorporated oxygen could lead to adverse effects on the bioactivity and mechanical properties of the prepared porous body. In this study, oxygen contamination during fabrication of bioactive porous bodies was measured. It was found that the oxygen content of the titanium metal was increased from 0.08 to 0.23 mass% when the porous body was prepared from bar stock, and it further increased up to 0.51 mass% when it was subjected to NaOH and heat treatments. Despite this, the porous bodies subjected to NaOH and heat treatments formed apatite on their pore walls within 1 day in a simulated body fluid. This result was consistent with the apatite-forming ability of NaOH- and heat-treated titanium plates with different oxygen contents in the range of 0.05 to 0.30 mass%. The compressive strength of the porous body was increased about 10% by the NaOH and heat treatments.     

Formation of bromo-substituted triclosan during chlorination by chlorine in the presence of trace levels of bromide

The side reactions of triclosan (2,4,4'-trichloro-2'-hydroxydiphenyl ether, TC) and chlorine in the presence of sodium chloride were investigated. In the absence of sodium chloride, three chloro-derivatives of TC, 2',3,4,4'-tetrachloro-2-hydroxydiphenyl ether (3-Cl-TC), 2',4,4',5-tetrachloro-2-hydroxydiphenyl ether (5-Cl-TC), and 2',3,4,4',5-pentachloro-2-hydroxydiphenyl ether (3,5-Cl(2)-TC) were formed, whereas in the presence of sodium chloride, 3-bromo-2',4,4'-trichloro-2-hydroxydiphenyl ether (3-Br-TC), 5-bromo-2',4,4'-trichloro-2-hydroxydiphenyl ether (5-Br-TC), (3 or 5)-bromo-2',4,4',(5 or 3)-chloro-2-hydroxydiphenyl ether ((3,5)-(BrCl)-TC), and 3,5-dibromo-2',4,4'-trichloro-2-hydroxydiphenyl ether (3,5-Br(2)-TC) were additionally formed. Radiochemical neutron activation analysis indicated that 1g of commercially available sodium chloride contained 73 microg of bromide and the bromide ion was determined to be the source of the side reactions. The rate of decrease of TC due to reaction with chlorine was greatly accelerated by the presence of bromide ion in the system: the rate with only 1 x 10(-5) M bromide ion was three times the rate in the absence of bromide.