The surface structure and composition of the low index single crystal faces of the ordered alloy Pt3Sn

The surface composition and structure of 111, 100, and 110 oriented single crystals of the ordered alloy Pt₃Sn (Ll₂ or Cu₃Au-type) were determined using the combination of low energy electron diffraction (LEED) and low energy ion scattering spectroscopy (LEISS). The clean annealed surfaces displayed LEED patterns and Sn/Pt LEISS intensity ratios consistent with the surface structures expected for bulk termination. In the case of the 100 and 110 crystals, preferential termination in the mixed (50% Sn) layer was indicated, suggesting this termination to be the consequence of a thermodynamic preference for tin to be at the surface.     

Dynamic mechanical properties of crosslinked polyisoprene under deformation

Summary Molecular motions of elastomers under deformations were observed through dynamic mechanical measurements. Composite master curves of dynamic moduli E and E and loss tangent tan over a wide range of frequency and in a state of elongation were obtained by the time-temperature superposition procedure. It is found that both moduli increase with strain, . The slope of the dispersion curve of E become more gradual with the increase in , while that of E is almost unchanged. The increment of E is generally larger than that of E, which does not agree with the N. W. Tschoegl prediction, E ^* ()=f() E _o ^* (), where E ^* () and E _o ^* () are complex moduli at the strain of and O, respectively, and f() is the function of only . The difference in the strain dependence of E from E was found to correspond to the strain dependence of the equilibrium modulus.     

Some Features of Gas‐Flame Propagation in Narrow Tubes

The dependence of the flamefront curvature on the composition of the mixture in tubes of various diameters is considered. The combustionwave velocities are measured for different fractions of fuel in the mixture. It is shown that the dependence of the burning velocity on the composition of the mixture has two maximums, one of them being related to the transition of the laminar combustion mode to turbulent combustion. Combustion turbulization is caused by flame instability to acoustic oscillations. Variations of the combustionwave shape due to acoustic oscillations are observed.     

Relationship between preferential adsorption coefficient and intrinsic viscosity in ternary systems

Summary The relation proposed between the preferential adsorption coefficient, , and the intrinsic viscosity, ¦¦ ¦¦=¦¦+AK has been applied in this paper to previously published data. This equation is found to be valid in theta condi tions and far away from them. The obtained results are compared to the ones calculated with the Dondos-Benoit equation.     

Interactions between pheromone traps with different strength lures for the pine beauty moth,Panolis flammea (Lepidoptera: Noctuidae)

Catches of malePanolis flammea in traps baited with lures containing 25 g of sex attractant are enhanced when in the proximity of traps baited with 125-g lures. The degree of enhancement is increased as the intertrap distance is decreased, and when the low-dose trap is upwind of the high-dose one. The patterns of alteration in trap catch suggest that moths initially attracted by one lure may divert into other traps, which may be either upwind of the original trap (overshooting), or downwind (undershooting). Overshooting can result in up to fivefold increases in catch and may provide a useful method for estimating the attractant zone of particular lure/trap combinations.     

Lamellar Thickness of a Syndiotactic Polystyrene Determined from Small-angle X-ray Scattering and Transmission Electron Microscopy

Extensive morphological studies on a syndiotactic polystyrene (sPS) sample prepared from compression molding were carried out using small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM). SAXS was conducted at 25C as well as at 150C to enhance the scattering contrast in order to obtain more reliable morphological parameters. The compression-molded sample was crystallized into a orthorhombic crystal lattice characterized by wide-angle X-ray diffraction (WAXD). A similar weight fraction of crystallinity, ca. 0.37, was obtained from both WAXD and differential scanning calorimetry measurements.In addition to the scattering peak at a scattering vector of ca. 0.36 nm^–1 attributable to the presence of lamellar/amorphous layers, anomalous scattering at the zero angle was found from the SAXS intensity profiles. Based on the Debye–Bueche theory, the scattering profile of this peculiar zero-angle scattering was deduced and was subtracted from the raw intensity profile to obtain the intensity profile exclusively associated with the lamellar/amorphous structure. A consistent long period was obtained for SAXS measured either at 25 or 150C, provided that the appropriate subtraction of intensities due to the zero-angle scattering was conducted. Moreover, the lamellar thickness deduced from the one-dimensional correlation function was in good agreement with TEM results. A difference scattering pattern derived from SAXS measured at 150 and 25C was obtained and a comparison of the morphological parameters was provided as well.     

Occurrence and Correlations of Monoterpene Hydrocarbon Enantiomers in Pinus sylvestris and Picea abies

The relative amounts and enantiomeric compositions of monoterpene hydrocarbons in branch and trunk xylem, in needles, and in resin from apical buds in 18 Pinus sylvestris trees have been determined and compared with the terpene content in branch xylem and needles of Picea abies. Besides the high amount of (+)-3-carene, an excess of (+)--pinene has been found in P. sylvestris, whereas in P. abies (–)--pinene dominates over (+)--pinene. In P. sylvestris, clear positive correlations were found between (+)--pinene and (+)-camphene in the four tissues analyzed. Good positive correlations were also observed between (–)--pinene and (–)-camphene in the two types of xylem, between (+)--pinene and (+)--pinene in the resin, and between tricyclene and (–)-camphene in resin and needles. In P. abies, positive correlations were found between (+)--pinene and (+)-camphene in the branch xylem and between tricyclene and (–)-camphene as well as between (–)--pinene and (–)-camphene in the needles. Complex relationships between (–)--pinene and (–)--pinene were found both in the P. abies and in the P. sylvestris tissues. The importance of the enantiomeric composition of -pinene for the host selection of Ips typographus, Tomicus piniperda, and Hylobius abietis is discussed.     

Convective Regime of Filtration Combustion of Energetic Materials in a Cocurrent Flow of Their Combustion Products

The convective regime of filtration combustion of energetic materials in a cocurrent flow of their combustion products is studied using a model with extremely simplified kinetics and heat transfer, which shows instability of the process. It is shown that the more accurate twotemperature model describes a steadystate regime. In this regime, the gas temperature on the hot boundary of the heating zone is well below the combustion temperature, and the solidphase temperature is well below the temperature proposed in recent studies on this topic. It is pointed out that the twotemperature approach is unjustified and intragranular nonisothermicity must be taken into account for convective regimes. It is shown that the threetemperature model, which takes into account this effect, does not give a stable steadystate solution.     

Processing of boron-nitrogen preceramic polymers

A number of new oligomeric and polymeric reagents rich in boron and nitrogen have recently been derived by several research groups. These reagents offer potential for the formation of boron nitride (BN) as controlled morphology powders as well as nonpowder forms. Specifically, it has been found that a family of 3-point and 2-point poly(borazinylamine) reagents may be processed by techniques used in organic polymer chemistry, with subsequent formation of BN ceramic fibers, coatings, xerogels, aerogels, and aerosols.     

Sequential extraction of nine trace elements from sludge-amended soils

Three separate samples taken from particular location of El-Gabal El-Asfar soils treated with composted sludge and irrigated with liquid sludge effluent were compared with untreated soil. These soils were sampled at 5 depths, i.e. 0–15, 15–30, 30–45, 45–60 and 60–75 cm to estimate the forms of nine trace metals in the solid phase. The soils had been amended with sewage sludge and irrigated with sludge liquids for different periods, i.e. 20, 40 and 60 years. The soil samples were fractionated by sequential extraction to estimate the quantities of these metals in exchangeable, sorbed organic, carbonate, and sulfide forms.Data reveal that most of these elements were concentrated (preferential fixation) in the surface layer (0–15 cm), possibly because of the slight decrease in soil apparent density resulting from sludge application. The trace metal contents in exchangeable and sorbed forms of most metals were very low. Sulfide, carbonate and organic forms were shown to be the dominant fractions for most trace metals under study and varied from one element to another. Nevertheless, at least 6 of these metals have a common behaviour.At the longterm addition of sludge application, the predominant metals were: Zn, Fe, Mn, Cr, Ni and Co in sulfide form; Cu in organic form, and Pb and Cd in the carbonate form.     

Structure of the Reaction Zone of a Steady Detonation Wave in Dinitrodiazapentane

The massvelocity profiles in 2,4dinitro2,4diazapentane samples of different densities were registered by a laser interferometer and the electromagnetic technique. The reaction time was shown to reach 300 nsec and weakly depend on density, while the pressure in the chemical spike can be twice as high as that at the Chapman–Jouguet point. No special features due to diamond formation were observed in the massvelocity profiles registered in the chemical reaction zone.     

Synthesis of new metal-containing side-chain monomers and polymers

New metal-containing vinyl monomers, hexyl-6-oxy-{4-[4-(4-carboxy cyclopentadienyl manganese tricarbonyl phenyl)phenyl]benzoyloxy}methacrylate and hexyl-6-oxy-{4-[4-(4-ferrocenoyl phenyl)phenyl]benzoyloxy}methacrylate, and the corresponding homopolymers and random copolymers with hydroxy monomer hexyl-6-oxy-{4-[4-(4-hydroxyphenyl)phenyl]benzoyloxy}methacrylate were synthesized. The compounds were characterized by¹H NMR; their thermal behavior was investigated by means of differential scanning calorimetry. Monomers and polymers containing the ferrocene unit melt at lower temperatures than those derived from the cyclopentadienyl managanese tricarbonyl moiety. The melting temperatures of the monomers and polymers ranged from 399 to about 515 K, Both monomers and polymers failed to exhibit mesogenic behavior. Values ofM _n,M _w,M _w/M _n, and degree of polymerization were obtained by gel permeation chromatography. TheM _n ranged from 16,500 for the copolymer containing hexyl-6-oxy-{4-[4-(4-ferrocenoyl phenyl)phenyl] benzoyloxy}methacrylate and hydroxy monomer hexyl-6-oxy-{4-[4-(4-hydroxyphenyl)phenyl]benzoyloxy}methacrylate at a 1:3 ratio to 26,000 for the copolymer containing hexyl-6-oxy-{4-[4-(4-carboxy cyclopentadienyl manganese tricarbonyl phenyl)phenyl]benzoyloxy}methacrylate and hydroxy monomer hexyl-6-oxy-{4-[4-(4-hydroxyphenyl)phenyl]benzoyloxy}methacrylate at a 1:3 ratio.M _w/M _n ranged from 1.6 in the case of the copolymer containing hexyl-6-oxy-{4-[4-(4-carboxy cyclopentadienyl manganese tricarbonyl phenyl)phenyl]benzoyloxy}methacrylate and hydroxy monomer hexyl-6-oxy-{4-[4-(4-hydroxyphenyl)phenyl]benzoyloxy}methacrylate at a 1:3 ratio to 2.2 in the case of poly(hexyl-6-oxy{4-[4-(4-carboxy cyclopentadienyl manganese tricarbonyl phenyl)phenyl]benzoyloxy}methacrylate).     

Formation of a phase structure of the “fibrils in matrix” type in a composite fibre based on high-density polyethylene and polyethylene terephthalate

Conclusions Regions of component ratio and conditions for obtaining a composite fibre of the fibrils in matrix type have been determined for the HDPE-PET system.At an HDPE-PET ratio of 60:40, phase inversion takes place and a structure of the interpenetration networks type is realized.Under identical fibre spinning conditions, the formation of a phase structure of the fibrils in matrix type can be regulated by varying the temperature.Translated from Khimicheskie Volokna, No. 4, pp. 38–40, July–August, 1987.     

Effect of distortions in the ideal profile of solid phase conductivity on performance efficiency of porouselectrodes

The effect of distortions in the ideal profile of the solid phase conductivity s(x) on porous electrode (PE) performance efficiency has been analysed using a one-dimensional model and an overall polarization curve involving both main and side reactions. Although an ideal electrically equally accessible PE is provided only by a hyperbolic profile s(x) passing through the middle of the electrode (the point s=L), it has been shown that a noticeable improvement in performance can be obtained using a rough approximation with any monotonic function providing a decrease in conductivity in the direction from the back current supply to the front plane of the PE, including functions not necessarily passing through the point s=L in the middle of the electrode. This permits less rigid requirements for the s(x) profile reproduction accuracy and simplification of experimental data acquisition.     

Cooperative inclusion of sodium 1-pyrenesulfonate by γ-cyclodextrin

Summary The interaction of -cyclodextrin(-CD) with sodium 1-pyrenesulfonate(PS) was studied spectrophotometrically. -CD was found to cause much larger decrease in the absorption maxima of PS than -CD. The fluorescence spectra of PS in the presence of -CD showed excimer emission, while those of PS with -CD showed only monomer emission, indicating that -CD forms 12 (-CDPS) complexes in which two PS molecules are included in the -CD cavity in a face-to-face fashion. The binding isotherm showed a sigmoidal curve. The association constants were estimated by computer simulation of the binding curve. The 12 (CDPS) complex was found to be much more stable (K=10⁶ M^–1) than the 11 complex (K=1 M^–1). At high concentration of -CD another -CD cooperates in binding two PS molecules, resulting in the formation of a 22 complex.     

Deposition of nanocrystals on flat supports by spin-coating

Monodisperse particles can be evenly distributed over flat supports by spin-impregnation. In this way Cu precursors have been deposited onto Si wafers. The effects of the rotation frequency and the concentration of the impregnation solution have been investigated. The mean diameter of the deposited particles can be varied from several nanometers upto several micrometers as is shown by microscopy images. Spin-impregnation appears a useful tool to prepare well-defined flat model catalysts, which are readily accessible both to quantitative characterisation and to catalytic testing.     

New polyisobutylene based model ionomers

Three-arm star polyisobutylene ionomers (¯M_n=8800) with terminal SO₃ M (M=K or Ca²) groups were synthesized and their mechanical properties investigated. Compression molded films displayed high elongations, i.e., -1000% for Ca² ionomers with lower values for the K counterions. Strain induced crystallinity was observed at higher elongations. Mechanical properties in general compared favorably with conventional covalently linked rubbery networks and were comparable and in some cases superior to EPDM-based ionomers carrying randomly distributed SO₃ M groups.For the first two parts see Proceedings, 28th IUPAC Macromolecular Symposium, Amherst, MA, July 11–16, 1982, p. 905 and 906     

Semi‐Empirical Method for Estimating the Combustion‐Wave Transition through the Contact Surface in a Composite Explosive

Through a comparison of experimental data on stable ignition and combustion of initial specimens composing igniter trains of pyrotechnic charges, critical conditions for combustionwave transition through the contact surface between neighboring compoundexplosive compacts are found. The evaluation procedure is tested with twenty explosives representing different combinations of five compacts of pyroxylin (guncotton), black gunpowder, and three types of pyrotechnic mixtures. Minimal dimensions of an interfacial protuberance promoting combustionwave propagation throughout the charge are found.     

Solutions of the general equations for the radiation dose dependence of the molecular weights of irradiated polymers with an initial Schulz-Zimm distribution

Summary The general equations for the radiation dose dependence of irradiated polymer molecular weights have been solved exactly. For an initial most probable molecular weight distribution (=1), the solutions are analytical and exact. For the general case (1) the solutions are numerical and exact. The present approach has resulted in the solutions for both =1 and 1 being incorporated into a group of FORTRAN computer programs which will solve experimental data for scission and crosslinking yields by both minimization and exact treatments. Simulated data treated using these FORTRAN programs are give. The FORTRAN programs are available from the authors.     

Inter-versus intramolecular oligomerization of nitrile groups in polyacrylonitrile

Summary Experimental evidence is presented indicating that intermolecular oligomerization of CN groups (leading to crosslinked structures) takes place, and possibly has an even greater importance than the intramolecular reaction (leading to ladder polymer), at higher temperatures. The easy, quasi built-in crosslinking upon heat treatment is considered the most significant single feature with regard to making polyacrylonitrile and its copolymers unique among synthetic polymers as a carbon fiber precursor.