Estimation of liquid film mass transfer coefficients for columns randomly packed with partially wetted rings

A semitheoretical correlation based on an extension of the random length, random angle statistical model of Davidson (1959) is developed which predicts liquid film mass transfer coefficients in a column packed with partially wetted Raschig rings. The method takes into account the ring size and the mixing which occurs at the packing junctions and allows an estimation of the effective length of a packing piece for a particular liquid viscosity. Predicted values of mass transfer coefficients are in good agreement with the experimental values obtained for the carbon dioxide-water and carbon dioxide-aqueous glycerol systems at 25°C reported by Mangers and Ponter (1980b) and other systems reported by Sherwood and Holloway (1940).     

Aqueous gel permeation chromatography: The effect of solvent ionic strength

Porous glass packing materials have been used for gel permeation chromatography using an aqueous phosphate buffer. Elution volumes were determined for polystyrene sulfonates, dextrans, and small neutral and charged molecules at three different ionic strengths, viz., 0.01M, 0.1M, and 1.0M phosphate, pH 7.0. The pore diameters of the glasses studied were 75, 240, 700, and 2000 Å. Elution volumes of nonionic species were unaffected by changing the solvent ionic strength. Elution volumes of charged species were markedly affected by the ionic strength of the solvent. This was attributed to a combination of decreased polymer dimensions and decreased ionic exclusion with increasing buffer concentration. The use of low ionic strength solvents may be exploited to tailor the separating range for polyelectrolytes with porous glass packings. This is particularly useful in the low molecular weight range where the lowest pore size available is 75 Å.     

"Alumina" Surface Modification of Silicon Nitride for Colloidal Processing

Two different methods are used to coat silicon nitride particles with an alumina precursor to make Si₃N₄ behave like Al₂O₃ in aqueous slurries. The first method involves the precipitation of an aluminum hydroxycarbonate from dissolved Al(NO₃)₃ during the decomposition of urea. In the second method, dry silicon nitride powder is reacted with aluminum tri- sec -butoxide in hexane at room temperature. Both methods produce a coated powder in which the electrophoretic and rheological properties of aqueous slurries mimic those of alumina. When salt is added to slurries consisting of coated Si₃N₄ powder, all rheological evidence suggests the presence of a short-range repulsive potential that produces a weakly attractive particle network similar to that previously reported for Al₂O₃ powder. Although electrophoretic and rheological data showed that the coated powder behaved like Al₂O₃, consolidation data indicated that slurries of coated powder with added salt did not pack to high density. In addition, these bodies were not plastic as found for bodies consolidated from dispersed and salt-added Al₂O₃ slurries.     

High-Temperature Structural Phase Transition in Ca0.7Ti0.7La0.3Al0.3O3: Investigation by Synchrotron X-Ray Diffraction

Mixed-oxide prepared Ca_0.7Ti_0.7La_0.3Al_0.3O₃ (CTLA) ceramics (≈96% dense), grain size 6–7 μm, with dielectric properties (at 4 GHz) of ɛ_r≈46, Q × f ≈38 000 GHz, and τ_f+13 ppm/°C, were studied at 25°–1300°C using synchrotron X-ray powder diffraction. At room temperature, CTLA exhibits a distorted orthorhombic structure, with two tilt systems: a =5.40383 (4) Å, b =5.41106 (6) Å, and c =7.64114 (7) Å with space group Pbnm . At 1050°±25°C, there is a transition from orthorhombic ( Pbnm ) to tetragonal ( I 4/ mcm ), with a simpler tilt arrangement. The lattice parameters at 1100°C were: a =5.44285 (4) Å and c =7.68913 (8) Å.     

Segregation in Single-Crystal Fully Stabilized Yttria-Zirconia

X-ray photoelectron spectroscopy (XPS) has been used to study surface segregation in 9.5 mol% single-crystal Y₂O₃-ZrO₂ which has been subjected to air anneals at temperatures ranging from 900° to 1500°C. The kinetics of segregation reveal an enrichment of Y, Si, Na, and Fe at short times; however, at longer times surface equilibrium is reached. The heats of segregation for Y, Si, Na and Fe, determined from Arrhenius plots, were 9.3 ± 3.0, 59.0 ± 7.0, –23.5 ± 11.5, –18.0 ± 6.0 kJ/mol, respectively. XPS analysis of the equilibrium states at all temperatures revealed a distinct surface layer which, given the positive heats of segregation for Si and Y, is quite stable.     

Induced Defensive Response of Myrtle Oak to Foliar Insect Herbivory in Ambient and Elevated Co2

The rising level of atmospheric CO2 has stimulated several recent studies attempting to predict the effects of increased CO2 on ecological communities. However, most of these studies have been conducted in the benign conditions of the laboratory and in the absence of herbivores. In the current study, we utilized large octagonal chambers, which enclosed portions of an intact scrub-oak community to investigate the interactive effects of CO2 and insect herbivory on myrtle oak, Quercus myrtifolia. Specifically, we assessed the effects of ambient and elevated CO2 (2x current concentrations) on percent foliar nitrogen, C:N ratio, total relative foliar tannin content, and the presence of leaf damage caused by leaf mining and leaf chewing insects that feed on myrtle oak. Total foliar N declined and C:N ratios increased significantly in oaks in elevated CO2 chambers. The percentages of leaves damaged by either leafminers or leaf chewers tended to be lower in elevated compared to ambient chambers, but they co-occurred on leaves less than expected, regardless of CO2 treatment. Leaves that had been either mined or chewed exhibited a similar wounding or defensive response; they had an average of 25 and 21% higher protein binding ability, which is correlated with tannin concentration, compared to nondamaged control leaves, respectively. While the protein-binding ability (expressed as total percent tannin) of leaves from elevated CO2 was slightly higher than from leaves grown in ambient chambers, this difference was not significant.     

Responses of fig wasps to host plant volatile cues

Fig wasps (Chalcidoidea; Agaonidae) are intimately associated with the 750 or so species of fig trees (Ficus, Moraceae). Each tree species is usually pollinated by a single species of wasp belonging to the subfamily Agaoninae, while other wasps of the family are parasitoids or seed predators. Previous experiments have shown that the wasps are attracted to the trees by volatiles emanating from the figs. Using fig-bearing trees and arrays of sticky traps baited with figs, we investigated the specificity of wasp attraction and its timing. The pollinators of two closely relatedFicus species were specifically attracted to figs of their host species and only at the time when figs were ready to be pollinated. Some nonpollinating fig wasps appear to respond to the same volatile cues.     

Ring position in cyclopropene fatty acids and stearic acid desaturation in hen liver

Four cyclopropene fatty acids, having the double bond of the cyclopropene ring at the 8,9, 9,10, 10,11 and 11,12 positions, respectively, were tested as inhibitors of stearic acid desaturation by the desaturase enzyme system of hen liver. The first three were powerful inhibitors, but the last was not. The cyclopropene acids with the 9,10 and 10,11 double bonds were equally strong inhibitors, while the acid with the 8,9 double bond was less effective. To account for the specificity of those cyclopropene fatty acids in which the C9 or C10 carbon atom is included in the cyclopropene ring, it is suggested that the conformation and structure of the CoA derivatives of these acids is such that they can irreversibly occupy the site on the enzyme responsible for 9,10-desaturation.     

Recent advances in molecular weight determination

The aging and lifetimes of polymeric materials depend on the reaction of these materials to the particular stresses which are applied. In many cases the molecular weight of the polymer is changed and this affords a way to follow aging phenomena. In the simplest case a homopolymer is subjected to a stress which increases or decreases its molecular weight without any chemical changes. As the situation becomes more complicated, changes in chemical composition occur and different sized molecular species are generated. These new species may be of extremely low molecular weight or they may be in the form of crosslinked gel. This paper reviews methods which are available for the determination of molecular weight and molecular weight distribution of polymeric materials. Recently developed or modified techniques are treated in more detail. Techniques which may be used to characterize the oligomer region or analyze for the presence of crosslinked gel are included.     

Effects of composition and phase relations on mechanical properties and crystallization of silicate glasses

Crystallization, mechanical properties, and workability are all important for the commercialization and optimization of silicate glass compositions. However, the inter-relations of these properties as a function of glass composition have received little investigation. Soda-lime-silica glasses with Na₂O-MgO-CaO-Al₂O₃-SiO₂ compositions relevant to commercial glass manufacture were experimentally studied and multiple liquidus temperature and viscosity models were used to complement the experimental results. Liquidus temperatures of the fabricated glasses were measured by the temperature gradient technique, and Rietveld refinements were applied to X-Ray powder diffraction (XRD) data for devitrified glasses, enabling quantitative determination of the crystalline and amorphous fractions and the nature of the crystals. Structural properties were investigated by Raman spectroscopy. Acoustic echography, micro-Vicker's indentation, and single-edge-notched bend testing methods were used to measure Young's moduli, hardness, and fracture toughness, respectively. It is shown that it is possible to design lower-melting soda-lime-silica glass compositions without compromising their mechanical and crystallization properties. Unlike Young's modulus, brittleness is highly responsive to the composition in soda-lime-silica glasses, and notably low brittleness values can be obtained in glasses with compositions in the wollastonite primary phase field: an effect that is more pronounced in the silica primary phase field. The measured bulk crystal fractions of the glasses subjected to devitrification at the lowest possible industrial conditioning temperatures indicate that soda-lime-silica glass melts can be conditioned close to their liquidus temperatures within the compositional ranges of the primary phase fields of cristobalite, wollastonite, or their combinations.