Silica hydride intermediate for octadecylsilica and phenyl bonded phase preparation via heterogeneous hydrosilation in supercritical carbon dioxide

Investigations into the preparation of silica hydride intermediate in supercritical carbon dioxide (sc-CO(2)) that avoids the use of organic solvents such as toluene or dioxane are described. The effects of reaction temperature, pressure and time on the surface coverage of the supercritical fluid generated silica hydride intermediate were studied. Under optimised supercritical conditions of 120°C, 483 bar and 3 h reaction time, silica hydride (Si-H) conversion efficiencies of ca. 40% were achieved for the hydride intermediate prepared from a monofunctional silane reagent (dimethylmethoxysilane). Si-H conversion efficiencies (as determined from (29)Si CP-MAS NMR spectral analysis) for the hydride intermediate prepared from triethoxysilane (TES) in sc-CO(2) were found to be comparable to those obtained using a TES silanisation approach in an organic solvent. (13)C and (29)Si CP-MAS-NMR spectroscopy was employed to provide a complete structural assignment of the silica hydride intermediates. Furthermore, supercritical CO(2) was subsequently employed as a reaction medium for the heterogenous hydrosilation of silica hydride with octadecene and with styrene, in the presence of a free radical initiator. These supercritical fluid generated reversed-phase materials were prepared in a substantially reduced reaction time (3 h) compared to organic solvent based methods (100 h reaction time). Silica functionalisation in sc-CO(2) presents an efficient and clean alternative to organic solvent based methods for the preparation of important silica hydride intermediate and silica bonded stationary phases via a hydrosilation approach.     

Retention and selectivity properties of carbamate pesticides on novel polar-embedded stationary phases

This study describes the use of stationary phases with polar functionality suitable for the chemical analysis of carbamates pesticides and comparing with conventional alkyl C8 and C18 phases. The emphasis of this study was to compare the selectivity and retention of the pesticides on different stationary phases, bonded onto 1.7 μm partially porous silica particles under isocratic separation condition. Four stationary phases including: phenylaminopropyl (PAP) phase, bidentate propylurea-C18 (BPUC₁₈), C8 and C18, were successfully bonded on the partially porous silica spheres as evidenced by ²⁹Si and ¹³C solid-state NMR analysis. The phenylaminopropyl phase exhibited smaller retentivity and enhanced selectivity compared to the alkyl C8 phase; the analysis time to run separation of the six carbamate pesticides (i.e., methomyl, propoxur, carbofuran, carbaryl, isoprocarb, and promecarb) on the PAP phase was threefold faster than alkyl C8 phase. In a similar manner, the BPUC₁₈ phase shows similar selectivity to that of the PAP phase, but with longer retentivity; although the BPUC₁₈ phase is characterized with a lesser degree of retentivity for the carbamate pesticides than the conventional alkyl C18 phase. We propose that π–π and weak polar interactions between the carbamate pesticides and the PAP phase dominates the separation mechanism and providing a superior selectivity; faster separation time was also achieved as a result of smaller retentivity. Whereas the C8 and C18 bonded phases exhibits only hydrophobic interactions with the pesticides, leading to larger retentivity. The BPUC₁₈ phase is shown to interact via polar–polar interactions in addition to hydrophobic interactions with the pesticides, providing similar selectivity with the PAP phase but with larger retentivity.     

Search with the ATLAS detector for new physics with significant missing transverse energy and two isolated leptons

Results of searches for supersymmetry in events with significant missing transverse energy and two isolated leptons with the ATLAS experiment at the LHC are presented. Three analyses are presented here, the first two are analyses with leptons of opposite charge and same charge, respectively. The third one is an analysis that searches for an excess of same-flavour opposite-charge lepton pairs over those of different-flavour. Data corresponding to an integrated luminosity of 1 fb^?1 are analysed.     

Probability Density Function of the Output Current of Cascaded Multiplexer/Demultiplexers in Transparent Optical Networks

The influence of the concatenation of arbitrary optical multiplexers/demultiplexers (MUX/DEMUXs) on the probability density function (PDF) of the output current of a transparent optical network is assessed. All PDF results obtained analytically are compared with estimates from Monte Carlo simulation and an excellent agreement is achieved.

The non-Gaussian behavior of the PDFs, previously reported by other authors for square-law detectors, is significantly enhanced with the number of nodes increase due to the noise accumulation along the cascade of MUX/DEMUXs. The increase of the MUX/DEMUXs bandwidth and detuning also enhances the PDFs non-Gaussian behavior. The PDF shape variation with the detuning depends strongly on the number of nodes.

Explanations for the Gaussian approximation (GA) accuracy on the assessment of the performance of a concatenation of optical MUX/DEMUXs are also provided. For infinite extinction ratio and tuned MUX/DEMUXs, the GA error probabilities are, in general, pessimistic, due to the inaccurate estimation of the error probability for both bits. For low extinction ratio, the GA is very accurate due to a balance between the error probabilities estimated for the bits “1” and “0.” With the detuning increase, the GA estimates can become optimistic.     

FEATURES AND APPLICATIONS OF BERTALANFFY-RICHARDS‘ AND SCHNUTE'S GROWTH EQUATIONS

ABSTRACT. Based on various ranges of the parameter m (or b), the paper analyzes the features and the integral forms of the Schnute and the Bertalanffy-Richards growth equations as well as the two aspects of their special cases (such as Gompertz, logistic and monomolecular models). It is a first attempt to investigate all the corresponding relationships among parameters of the models derived from the Schnute and the Bertalanffy-Richards growth equations. All the models from the two are empirically fitted by different data sets for eucalypt plantations. Unlike earlier papers, the results of this paper show that either of the two growth equations can be considered as a model for estimating forest growth given a parameter range, and both can produce similar growth performances. Some other aspects of the two growth equations are discussed so that the two can be used correctly.     

Abelianization of the <Emphasis Type="Italic">F</Emphasis>-divided fundamental group scheme

Let (X , x ₀) be a pointed smooth proper variety defined over an algebraically closed field. The Albanese morphism for (X , x ₀) produces a homomorphism from the abelianization of the F-divided fundamental group scheme of X to the F-divided fundamental group of the Albanese variety of X. We prove that this homomorphism is surjective with finite kernel. The kernel is also described.     

Cyclodextrin‐modified capillary electrophoresis for achiral and chiral separation of ergostane and lanostane compounds extracted from the fruiting body of Antrodia camphorata

A CD‐modified capillary electrophoretic method has been developed for achiral and chiral analysis of seven bioactive compounds isolated from the fruiting body of Antrodia camphorata. Such important target analytes exhibit similar chemical structures and are known for their diverse properties including antioxidant and anticancer effects. The analytes were separated in 25 min using a pH 9.3, 20 mM sodium borate buffer containing 20 mM methyl‐β‐CD and 30 mM sulfobutylether‐β‐CD. With the exception of the optical isomer pairs (antcin B or zhankuic acid A, zhankuic acid C, and antcin A), the remaining bioactive compounds including the chiral pair antcin C were baseline‐separated. Analysis time was noticeably longer to baseline separate all of the above chiral pairs (～38 min) by adding 5% DMF to the running buffer. The migration order was reversed compared with the HPLC elution. More hydrophobic compounds complexed favorably with methyl‐β‐CD and emerged earlier in the electropherogram than their more hydrophilic counterparts which were strongly associated with sulfobutylether‐β‐CD. The simple capillary electrophoretic method developed was applicable for rapid separation and characterization of several important bioactive compounds isolated from the fruiting body of A. camphorata.     

LED照射光催化剂用于苯、甲苯、乙苯和二甲苯分解(英文)

Studies on the use of gas phase applications of light emitting diodes(LEDs) in photocatalysis are scarce although their photocatalytic decomposition kinetics of environmental pollutants are likely different from those in aqueous solutions.The present study evaluated the use of chips of visible light LEDs to irradiate nitrogen doped titania(N-TiO2) prepared by hydrolysis to decompose gaseous benzene,toluene,ethyl benzene,m-xylene,p-xylene,and o-xylene.Photocatalysts calcined at different temperatures were characterized by various analytical instruments.The degradation efficiency of benzene was close to zero for all conditions.For the other compounds,a conventional 8 W daylight lamp/N-TiO2 unit gave a higher photocatalytic degradation efficiency as compared with that of visible-LED/N-TiO2 units.However,the ratios of degradation efficiency to electric power consumption were higher for the photocatalytic units that used two types of visible-LED lamps(blue and white LEDs).The highest degradation efficiency was observed with the use of a calcination temperature of 350 oC.The average degradation efficiencies for toluene,ethyl benzene,m-xylene,p-xylene,and o-xylene were 35%,68%,94%,and 93%,respectively.The use of blue-and white-LEDs,high light intensity,and low initial concentrations gave high photocatalytic activities for the photocatalytic units using visible-LEDs.The morphological and optical properties of the photocatalysts were correlated to explain the dependence of photocatalytic activity on calcination temperature.The results suggest that visible-LEDs are energy efficient light source for photocatalytic gas phase applications,but the activity depends on the operational conditions.     

发光二极管用于活性炭负载光催化剂反应器中挥发性有机化合物的降解

The applicability of ultraviolet-light emitting diodes(LEDs)as a light source for photocatalysis using granular activated charcoal (GAC)impregnated with transition metal-enhanced photocatalysts for the control of volatile organic compounds(VOCs)was investigated. Two target compounds(toluene and methyl mercaptan)were selected to evaluate the removal activities of the TiO2/GAC composites.The photocatalysts were prepared by a sol-gel method.Methyl trimethoxy silane was added as a precursor sol solution to bind...     

Glass Formation Ability and Kinetics of the Gd55A120Ni25 Bulk Metallic Glass

We report a new bulk glass-forming alloy GdssA12oNi25. The bulk sample of the alloy is prepared in the shape of rods in diameter 2ram by suction casting. The rod exhibits typical amorphous characteristics in the x-ray diffraction pattern, paramagnetic property at 30OK, distinct glass transition and multi-step crystallization behaviour in differential scanning calorimetry traces. The gJass formation ability of the alloy is investigated by using the reduced glass transition temperature Trg and the parameter γ- Kinetics of glass transition and primary crystallization is also studied. The fragility parameter m obtained from the Vogel-Fulcher-Tammann dependence of glass transition temperature Tg on In φ （φ is the heating rate） classifies the bulk metallic glasses into the intermediate category according to Angell＇s classification.