Strain-Free Total Resonant Sextet Benzenoid Hydrocarbons

The importance of strain-free (total) resonant sextet benzenoid hydrocarbons is pointed out. The first computer-aided generation and enumeration of such systems is reported, and the data represent substantial supplements to the previous numbers of strain-free resonant sextet benzenoid isomers. Supplementary depictions of some forms of the systems in question are also provided. Constant-isomer series are delineated for the resonant sextet benzenoids. The numbers associated with these series are found to match exactly the known numbers for corresponding constant-isomer series of strictly pericondensed benzenoids.     

Issues in the mapping of two diseases

Recently, there has been increased interest in the geographical modelling of two or more diseases. In this article, we consider a number of issues relating to such an endeavour including the standardization process and the comparison of univariate and bivariate disease mapping models. A principle motivation for the examination of two or more diseases is to discover similarities or dissimilarities in the geographical distribution of risk. In this article, we propose a proportional mortality approach to give clues to areas of similarity and dissimilarity. A secondary aim of bivariate modelling is to 'borrow strength' between diseases in order to provide better estimates of risk in each area. We will illustrate various modelling strategies using incidence data from 1996 to 2000 on lung and bladder cancer in Washington state.     

Supertoughness in Polysulfone/Poly(ethylene‐octene) Blends

Summary: Poly(sulfone of Bisphenol A) (PSU) based blends were obtained by melt blending PSU with up to 15 wt.‐% poly(ethylene‐octene) either modified with maleic anhydride (mPEO) or not (PEO). The dispersed particle size was small and similar in blends with PEO or mPEO. These facts indicated respectively that the interfacial tension was low and the lack of compatibilizing effect of mPEO. Some preferential presence of PEO in the outer surface of the specimens was observed, and was attributed to the large viscosity difference between the two components of the blends. This had no effect on the modulus of elasticity, but speeded up both the yield stress and ductility decreases at rubber contents above 3.25 wt.‐%. However, despite the immiscibility of the components, and thanks to the small particle size of the blends, super‐toughness was attained in the unmodified PSU/PEO blends. This was at PEO contents (3.25 wt.‐%) at which the modulus, yield stress and ductility of the blends were almost as good as those of pure PSU. It appeared that a change of the chemical nature of the rubber did not influence by itself super‐toughness, unless it was accompanied by either a morphological or adhesion change.

Impact strength of PSU‐based blends vs. PEO (○) or mPEO (?) content.     

Preparation of Sputtered (Bax,Sr1−x)TiO3 Thin Films Directly on Copper

(Ba_0.6,Sr_0.4)TiO₃ (BST) films were deposited on copper foils by radio frequency magnetron sputtering. By the use of controlled p O₂ high-temperature anneals, the films were completely crystallized in the absence of substrate oxidation. X-ray diffraction and transmission electron microscopy (TEM) revealed an abrupt Cu/BST interface. The deposited BST films exhibit a zero bias permittivity and loss tangent values of 600 and 0.018, respectively. An electrical tunability ratio of 3.5:1 is observed on these metal–insulator–metal devices. Devices show leakage currents of 10⁻⁸ A/cm² at ±10 V/μm, and loss tangents as low as 0.003 in fields approaching 40 V/μm.     

Carbon membranes from cellulose and metal loaded cellulose

The focus of this work was to find a low-cost precursor for carbon molecular sieve (CMS) membranes, and a simple way of producing them. In addition, several ways of modifying a carbon material are described. The modification method used in this study was metal doping of carbon. CMS membranes were formed by vacuum carbonization of cellulose and metal loaded cellulose. Metal additives include oxides of Ca, Mg, Fe(III) and Si, and nitrates of Ag, Cu and Fe(III).The carbon membrane containing Fe-nitrate has promising separation performance for the gas pairs O₂/N₂ and CO₂/CH₄. Carbon containing nitrates of Cu or Ag show high selectivity, but reduced O₂ and CO₂ permeability compared to carbon with Fe-nitrate. Element analysis indicates that Cu migrates to the carbon surface, creating an extra layer resistance to gas transport. A silver mirror is also seen on the surface of Ag-nitrate-containing carbon. However, the Ag- and Cu-containing membranes show a high H₂ permeability. Adding metal oxides makes the carbon membranes retard the transport of easily condensable gases (e.g. CO₂). This can be exploited for enhanced H₂/CO₂ separation efficiency.     

Simple N‐Heterocyclic Carbenes as Ligands in Ullmann‐Type Ether and Thioether Formations

A simple N‐heterocyclic carbene (NHC) derived from 1‐methyl‐3‐ethylimidazolium tetrafluoroborate was found to be an efficient ligand for a range of copper‐catalyzed cross‐coupling reactions, leading to the formation of aromatic ethers and thioethers.

     

The speed of sound and isentropic bulk modulus of biodiesel at 21°C from atmospheric pressure to 35 MPa

Biodiesel, an alternative diesel fuel consisting of the alkyl monoesters of fatty acids from vegetable oils and animal fats, can be used in existing diesel engines without modification. However, property changes associated with the differences in chemical structure between biodiesel and petroleumbased diesel fuel may change the engine's injection timing. These injection timing changes can change the exhaust emissions and performance from the optimized settings chosen by the engine manufacturer. This study presents the results of measurements of the speed of sound and the isentropic bulk modulus for methyl and ethyl esters of fatty acids from soybean oil and compares them with No. 1 and No. 2 diesel fuel. Data are presented at 21±1°C and for pressures from atmospheric to 34.74 MPa. The results indicate that the speed of sound and bulk modulus of the monoesters of soybean oil are higher than those for diesel fuel and these can cause changes in the fuel injection timing of diesel engines. Linear equations were used to fit the data as a function of pressure, and the correlation constants are given.     

Hydrothermal conversion of FAU zeolite into aluminous MTN zeolite

The hydrothermal conversion of FAU zeolite into aluminous MTN zeolite is described here. In the presence of both benzyltrimethylammonium hydroxide (BTMAOH) and sodium chloride (NaCl) the highly crystalline and pure MTN zeolites with Si/Al ratios of 21-23 could be obtained from the hydrothermal conversion of FAU zeolite. Based on powder XRD refinement and ¹³C CP/MAS NMR spectra, BTMA⁺ ions were not present in cages of the obtained zeolites, but TMA⁺ ions existed instead. It means that BTMAOH underwent degradation during the conversion. Moreover, the effects of Si/Al ratio of starting FAU zeolite, synthesis parameters (BTMAOH/SiO₂ and H₂O/SiO₂ ratios) and the addition of alkali metal chlorides on the hydrothermal conversion of FAU zeolite into MTN zeolite are discussed. As compared to amorphous SiO₂/γ-Al₂O₃, which produced impurity, the hydrothermal conversion of FAU zeolite showed a fast crystallization rate and a high selectivity to MTN zeolite formation. These phenomena indicate that the assembly of locally ordered aluminosilicate species coming from the decomposition or dissolution of FAU zeolite should be taking part in the conversion process.