Size-controlled simple fabrication of free-standing, ultralong metal nanobelt array

Free-standing, ultralong (up to several millimeters) nanobelts of gold, silver, and copper were fabricated by a template approach. Firstly, a metal nanofin array was prepared on a substrate via metal nanocoating of the template surface and selective removal of the metal top layer and template. Electroless plating and sputtering were employed for the metal nanocoating. In this approach, the minimum width and thickness of the Au nanobelt were 95 and 30 nm, respectively. Systematic control of the nanobelt width (from 95 to 350 nm) was successfully achieved by adjusting the template height. Free-standing nanobelts of several millimeters in length were fabricated and maintained their unique structure and alignment, even on a mesh grid.     

Anomalous transport properties of the half-metallic ferromagnets Co₂TiSi, Co₂TiGe and Co₂TiSn

In this work, the theoretical and experimental investigations of Co?TiZ (Z=Si, Ge or Sn) compounds are reported. Half-metallic ferromagnetism is predicted for all three compounds with only two bands crossing the Fermi energy in the majority channel. The magnetic moments fulfil the Slater-Pauling rule and the Curie temperatures are well above room temperature. All compounds show a metallic-like resistivity for low temperatures up to their Curie temperature, above the resistivity changes to semiconducting-like behaviour. A large negative magnetoresistance (MR) of 55 per cent is observed for Co?TiSn at room temperature in an applied magnetic field of μ(0)H=4T, which is comparable to the large negative MRs of the manganites. The Seebeck coefficients are negative for all three compounds and reach their maximum values at their respective Curie temperatures and stay almost constant up to 950?K. The highest value achieved is -52?μVK(-1) for Co?TiSn, which is large for a metal. The combination of half-metallicity and the constant large Seebeck coefficient over a wide temperature range makes these compounds interesting materials for thermoelectric applications and further spincaloric investigations.     

Effect of rare earth oxides for improvement of MCFC

The solubility of rare earth metal oxides and their effect on the NiO solubility have been discussed to stabilize the cathode of molten carbonate fuel cells. The solubility of Ho, Yb, and Nd oxides were 4.4 × 10⁻⁴, 3.4 × 10⁻⁴, and 1.3 × 10⁻³ (mole fraction) at 923 K, respectively. The solubilities of NiO in (Li_0.52/Na_0.48)₂CO₃ with the saturated Ho, Yb, and Nd were 1.57 × 10⁻⁵, 1.41 × 10⁻⁵, and 9.5 × 10⁻⁶, respectively. Among these three, Nd, which has the highest solubility in the carbonates, reduced the NiO solubility most; although, the La reduced the NiO solubility more than Nd.

The logarithm of the solubility of the rare earth metal oxides has a linear relation to the Coulomb force ratio between the rare earth metal and the alkaline metal. Following this relation, the La should have the highest solubility among all the lanthanides. The basicity which NiO solubility closely relates has a linear relationship to the Coulomb force parameter of the melts. Based on these two models, the La would be the best additive to reduce the NiO solubility in Li/Na eutectic carbonate melt, among all the lanthanides.     

Xylanase-Resistant Xylan In Unbleached Kraft Pulp

A water-soluble chromophoric xylanase-resitant xylan fraction (LF-D) was separated from a hardwood unbleached kraft pulp (UKP) after hydrolysis with a cellulase/ xylanase-membrane bioreactor. LF-D contained over 70% unremovable inorganic atoms including Si, Na, and S, together with a β-1,4- linked xylan. A nucleus exchange reaction and a nitrobenzene oxidation showed that LF-D contained a trace amount of a lignin component abundant in quinoid structures which had been partly demethylated during the course of kraft pulping. On the other hand, a higher molecular weight residual lignin fraction (HF-P), which was obtained from an impermeable part of the enzymatic digests, was found to have a diphenylmethane structure. LF-D was partially decolorized by Coriolus versicolor and bacterial microflora without action of extracellular lignin peroxidase, Mn-peroxidase, laccase or xylanase.     

Antioxidant Activity of Phenolic Compounds from Fava Bean Sprouts

Fava beans are eaten all over the world and recently, marketing for their sprouts began in Japan. Fava bean sprouts contain more polyphenols and l ‐3,4‐dihydroxyphenylalanine (l ‐DOPA) than the bean itself. Our antioxidant screening program has shown that fava bean sprouts also possess a higher antioxidant activity than other commercially available sprouts and mature beans. However, the individual constituents of fava bean sprouts are not entirely known. In the present study, we investigated the phenolic compounds of fava bean sprouts and their antioxidant activity. Air‐dried fava bean sprouts were treated with 80% methanol and the extract was partitioned in water with chloroform and ethyl acetate. HPLC analysis had shown that the ethyl acetate‐soluble parts contained phenolic compounds, separated by preparative HPLC to yield 5 compounds ( 1 ? 5 ). Structural analysis using NMR and MS revealed that the compounds isolated were kaempferol glycosides. All isolated compounds had an α‐rhamnose at the C‐7 position with different sugars attached at the C‐3 position. Compounds 1 ? 5 had β‐galactose, β‐glucose, α‐rhamnose, 6‐acetyl‐β‐galactose and 6‐acetyl‐β‐glucose, respectively, at the C‐3 position. The amount of l ‐DOPA in fava bean sprouts was determined by the quantitative ¹H NMR technique. The l ‐DOPA content was 550.45 mg ± 11.34 /100 g of the raw sprouts. The antioxidant activities of compounds 2 ? 5 and l ‐DOPA were evaluated using the 2,2‐diphenyl‐1‐picrylhydrazyl scavenging assay. l ‐DOPA showed high antioxidant activity, but the isolated kaempferol glycosides showed weak activity. Therefore, it can be suggested that l ‐DOPA contributed to the antioxidant activity of fava bean sprouts.     

Co-effect of Mechanical Ball-milling and Microenvironmental Polarity on Morphology and Properties of Nanocellulose

Cellulose is a linear polymer consisting of D-anhydroglucose units joined by β-1,4-glycosidic linkages. The densely packed cellulose molecular chain forms crystalline cellulose through strong hydrogen bonding. Owing to its chemical tunability and excellent mechanical resistance, nanocellulose is widely used in everyday life and the industrial sector. In this work, cellulose materials were nanoprocessed by mechanical ball-milling(1) in polar solvents(N,N-dimethylformamide or dimethyl sulfoxide) with esterification or(2) in hydrophobic agents(polydimethylsiloxane or polytetrafluoroethylene) with different molecular weights. Cellulose nanofibers and nanosheets with different hydrophilic and hydrophobic properties were obtained, and the mechanism of cellulose disintegration along a crystallographic plane induced by mechanical force and the polarity condition were discussed. This work affords a new way to manipulate the morphology and properties of nanocellulose.     

Site-specific cleavage of MS2 RNA by a thermostable DNA-linked RNase H

A series of DNA-linked RNases H, in which the 15-mer DNA iscross-linked to the Thermus thermophilus RNase HI (TRNH) variantsat positions 135, 136, 137 and 138, were constructed and analyzedfor their abilities to cleave the complementary 15-mer RNA.Of these, that with the DNA adduct at position 135 most efficientlycleaved the RNA substrate, indicating that position 135 is themost appropriate cross-linking site among those examined. Toexamine whether DNA-linked RNase H also site-specifically cleavesa highly structured natural RNA, DNA-linked TRNHs with a seriesof DNA adducts varying in size at position 135 were constructedand analyzed for their abilities to cleave MS2 RNA. These DNAadducts were designed such that DNA-linked enzymes cleave MS2RNA at a loop around residue 2790. Of the four DNA-linked TRNHswith the 8-, 12-, 16- and 20-mer DNA adducts, only that withthe 16-mer DNA adduct efficiently and site-specifically cleavedMS2 RNA. Primer extension revealed that this DNA-linked TRNHcleaved MS2 RNA within the target sequence.     

Nucleate boiling of low-concentration alcohol aqueous solutions for the development of thermal management systems in space

To develop high-performance space thermal management systems using boiling phenomena, the heat transfer characteristics of low concentration alcohol aqueous solutions were investigated on ground. For mixtures of 1-Propanol/Water, 2-Propanol/Water and Water/1-Butanol, i.e. substantially positive mixtures at very low concentration range of alcohol, heat transfer enhancement was observed, while only heat transfer deterioration was reported in most of existing studies for nucleate boiling of mixtures. A concept of coexisting heat transfer enhancement due to Marangoni effect additionally to the heat transfer deterioration due to mass transfer resistance was emphasized. The concept seems to be true for mixture nucleate boiling independent of gravity level.     

Preparation and characterization of inexpensive heterogeneous catalysts for air pollution control: Two case studies

Relatively inexpensive heterogeneous catalysts for two reactions of great importance in air pollution control, NO reduction and VOC combustion, were prepared and characterized. Apart from their common practical goal and the frequent need for simultaneous removal of air pollutants, these reactions share a similar redox mechanism, in which the formulation of more effective catalysts requires an enhancement of oxygen transfer.

For NO reduction, supported catalysts were prepared by adding a metal (Cu, Co, K) using ion exchange (IE) and incipient wetness impregnation (IWI) to chars obtained from pyrolysis of a subbituminous coal. The effects of pyrolysis temperature, between 550 and 1000 °C, on selected catalyst characteristics (e.g., BET surface area, XRD spectrum, support reactivity in O₂) are reported. For IE catalysts, the surface area increased in the presence of the metals while the opposite occurred for IWI catalysts. For the Co-IE catalysts, the highest surface area was obtained at 700 °C. The XRD results showed that, except for Cu (which exhibited sharp Cu⁰ peaks), the catalysts may be highly dispersed (or amorphous) on the carbon surface. For the C–O₂ reaction the order of (re)activity was K  Co > Cu for IE catalysts and K > Cu > Co for IWI catalysts. For NO reduction the orders were K > Co > Cu (IE catalysts) and Cu > Co > K (IWI catalysts). In all cases the catalytic (re)activity for NO reduction was lower than that exhibited for the C–O₂ reaction. The K-IE and Cu-IWI catalysts appeared to be the most promising ones, although further improvements in catalytic activity will be desirable. Some surprising results regarding CO and CO₂ selectivity are also reported, especially for Co catalysts.

In VOC combustion, the effect of the nature of ion B (Fe and Ni) on the partial substitution of ion A (Ca for La) in ABO₃ perovskites (e.g., LaFeO₃ and LaNiO₃) and on their catalytic activity was studied. The perovskite-type oxides were characterized by means of surface area measurements, XRD, temperature-programmed desorption (TPD) and temperature-programmed reduction (TPR). The effect of partial substitution of La³⁺ by Ca²⁺ was more significant for the La_1−xCa_xFeO₃ perovskites. In this case, the electronic perturbation is compensated by an oxidation state increase of part of Fe³⁺ to Fe⁴⁺. The TPD results revealed that, at higher substitution levels, oxygen vacancies are also formed to preserve electroneutrality. For the La_1−xCa_xNiO₃ perovskites, the characterization results showed no evidence of large differences in electronic properties as calcium substitution increases. The La_1−xCa_xNiO₃ perovskites exhibited lower activity than the simple LaNiO₃ perovskite, whereas for the La_1−xCa_xFeO₃ substituted perovskites the most active catalyst (exhibiting the lowest ignition temperature) was obtained at the highest substitution level, La_0.6Ca_0.4FeO₃.

The performance of both groups of catalysts is briefly discussed in terms of redox processes, in which the interplay between oxygen transfer and electron transfer requires further elucidation for the improvement of catalytic activity.