Ascorbic Acid-Assisted Eco-friendly Synthesis of NiCo<Subscript>2</Subscript>O<Subscript>4</Subscript> Nanoparticles as an Anode Material for High-Performance Lithium-Ion Batteries

We have synthesized NiCo₂O₄ nanoparticles (NCO NPs) using an ascorbic acid-assisted co-precipitation method for the first time. When NCO NPs are used as an anode material for lithium-ion batteries, the cell exhibits superior lithium storage properties, such as high capacity (700 mA h g^?1 after 300 cycles at 200 mA g^?1), excellent rate capabilities (applied current density range 100–1200 mA g^?1), and impressive cycling stability (at 1200 mA g^?1 up to 650 cycles). The enhanced electrochemical properties of NCO NPs are due to the nanometer dimensions which not only offers a smooth charge-transport pathway and short diffusion paths of the lithium ions but also adequate spaces for volume expansion during Li storage. Hence, this eco-friendly synthesis approach will provide a new strategy for the synthesis of various nanostructured metal oxide compounds, for energy conversion and storage systems applications.     

A Binary Gas Transport Model Improves the Prediction of Mass Transfer in Freeze Drying

Monitoring partial vapor pressure in the freeze-drying chamber is a cheap, global, and non-intrusive way to assess the end of the primary drying stage. Most existing dynamic freeze-drying models which predict this partial pressure describe mass transfer between the product and the condenser via a mass transfer resistance or a mass transfer coefficient. Experimental evidence suggests that such models can be significantly in error for some values of the sublimation flux, leading to physically inconsistent predictions and possibly incorrect assessment of primary drying termination, with potential risk of product damage if moving to secondary drying and increasing shelf temperature while some ice is still present. Assuming a binary gas transport model for vapor and inert gas leads to improved and consistent predictions and explains the apparent variation of the mass transfer resistance with total pressure, shelf temperature, and product sublimation area.     

Improved evidence for the existence of an intermediate phase during hydration of tricalcium silicate

Tricalcium silicate (Ca₃SiO₅) with a very small particle size of approximately 50 nm has been prepared and hydrated for a very short time (5 min) by two different modes in a paste experiment, using a water/solid-ratio of 1.20, and by hydration as a suspension employing a water/solid-ratio of 4000. A phase containing uncondensed silicate monomers close to hydrogen atoms (either hydroxyl groups or water molecules) was formed in both experiments. This phase is distinct from anhydrous tricalcium silicate and from the calcium-silicate-hydrate (C-S-H) phase, commonly identified as the hydration product of tricalcium silicate. In the paste experiment, approximately 79% of silicon atoms were present in the hydrated phase containing silicate monomers as determined from ²⁹Si{¹H} CP/MAS NMR. This result is used to show that the hydrated silicate monomers are part of a separate phase and that they cannot be attributed to a hydroxylated surface of tricalcium silicate after contact with water. The phase containing hydrated silicate monomers is metastable with respect to the C-S-H phase since it transforms into the latter in a half saturated calcium hydroxide solution. These data is used to emphasize that the hydration of tricalcium silicate proceeds in two consecutive steps. In the first reaction, an intermediate phase containing hydrated silicate monomers is formed which is subsequently transformed into C-S-H as the final hydration product in the second step. The introduction of an intermediate phase in calculations of the early hydration of tricalcium silicate can explain the presence of the induction period. It is shown that heterogeneous nucleation on appropriate crystal surfaces is able to reduce the length of the induction period and thus to accelerate the reaction of tricalcium silicate with water.     

Squeezing-to-dripping transition for bubble formation in a microfluidic T-junction

The aim of this paper is to investigate the squeezing-to-dripping transition for bubble formation in a microfluidic T-junction by cross-flowing rupture technique using a high-speed digital camera. Experiments were conducted in a glass microfluidic T-junction with the cross-section of the microchannel of 120 μm wide and 40 μm deep. N₂ bubbles were generated in glycerol–water mixtures with several concentrations of surfactant sodium dodecyl sulfate (SDS). Three different regimes were identified for generating different kinds of bubbles: squeezing, dripping and transition regimes. Various forces exerted on the gaseous thread in different regimes were analyzed. Long slug bubbles were formed in the squeezing regime, while dispersed bubbles in the dripping regime. The transition regime formed short slug bubbles. The bubble sizes in various regimes could be correlated with several dimensionless numbers such as the ratio of gas/liquid flow rates and capillary number. The two-step model for droplets (Steegmans et al., 2009) was extended to describe the bubble formation.     

From relative to absolute quantification of tryptic peptides with tandem mass tags: application to cerebrospinal fluid

Quantification is a major task in proteomics. Among the different analytical strategies to enable peptide and protein quantification, tagging with isotopic labels has emerged as a practical, versatile, and efficient alternative. In particular, isobaric labels, such as TMT or iTRAQ, are now widely employed to make relative comparison of the protein amounts in separate biological samples with tandem mass spectrometry (MS/MS). We used herein a shotgun proteomic approach based on labelling with tandem mass tags (TMTs) for the relative quantification of proteins, and the absolute quantification of their tryptic peptides in human cerebrospinal fluid (CSF). First, the comparison of ante- and post-mortem CSF samples was carried out for the discovery of protein marker candidates of brain-damage disorders. Second, tryptic peptides representative of these candidates were measured in CSF using reporter-ion calibration curves. These works highlighted the advantages and limitations of such strategies for quantification purposes in proteomics.     

Sunflower oil coating on the nanoparticles of iron(III) oxides

High-temperature solution phase reaction of iron(III)-furoate in sunflower oil, in the presence of trichloroacetic acid and 1,2-hexadecylamine leads to iron(III) oxide (amorphous and γ-Fe2O3) nanoparticles with sizes about 1.3 nm in diameter (method “A”), and about 5.5 nm (amorphous Fe2O3) from the “sunflower oil/oxadiazol” system (method “B”).     

Thermal denaturation and aggregation of Myosin subfragment 1 isoforms with different essential light chains

We compared thermally induced denaturation and aggregation of two isoforms of the isolated myosin head (myosin subfragment 1, S1) containing different "essential" (or "alkali") light chains, A1 or A2. We applied differential scanning calorimetry (DSC) to investigate the domain structure of these two S1 isoforms. For this purpose, a special calorimetric approach was developed to analyze the DSC profiles of irreversibly denaturing multidomain proteins. Using this approach, we revealed two calorimetric domains in the S1 molecule, the more thermostable domain denaturing in two steps. Comparing the DSC data with temperature dependences of intrinsic fluorescence parameters and S1 ATPase inactivation, we have identified these two calorimetric domains as motor domain and regulatory domain of the myosin head, the motor domain being more thermostable. Some difference between the two S1 isoforms was only revealed by DSC in thermal denaturation of the regulatory domain. We also applied dynamic light scattering (DLS) to analyze the aggregation of S1 isoforms induced by their thermal denaturation. We have found no appreciable difference between these S1 isoforms in their aggregation properties under ionic strength conditions close to those in the muscle fiber (in the presence of 100 mM KCl). Under these conditions kinetics of this process was independent of protein concentration, and the aggregation rate was limited by irreversible denaturation of the S1 motor domain.     

本地化的生态建筑 法国罗纳-阿尔卑斯大区展馆的启示

文章介绍了2010年上海世博会法国罗纳-阿尔卑斯大区展馆和设计者的生态建筑本地化策略、相应的材料选择与技术应用等内容,作为面向未来城市的发展理念在上海的一次实施,该展馆对于本地发展具有一定的启示意义。     

A 1.4GS/s 9-bit 45 dB power control RFDAC for digital radio transmitters

This paper presents a high speed, 9-bit RF Digital-to-Analog Converter based on a new architecture implemented in a 0.13 μm BiCMOS process and able to adjust the output power by 45 dB to meet gain control requirements of the new communications standards with a SFDR >25 dBc. The maximum test-demonstrated frequency is 1.4 GHz and the chip dissipates <25 mW.     

Fully integrated blue/UV SOI CMOS photosensor for biomedical and environmental applications

In this paper, we present a microsystem for measuring optical power in blue/UV wavelengths (from λ = 200 nm to λ = 450 nm) which includes a photodiode and the analog processing circuit of the photodiode signal, fully integrated in 2 μm SOI CMOS technology. The photodiode has a maximum responsivity for λ = 400 nm. Th photosensor functions as a current to frequency converter. Measurements of the microsystem illuminated by blue and UV LEDs demonstrate the good linear behavior, sensitivity and efficiency of the system.