Degradation of Nextel™ 610‐based oxide‐oxide ceramic composites by aluminum oxychloride decomposition products

Nextel? 610 alumina fibers and alumina‐YAG (yttrium‐aluminum garnet) matrices were used to make oxide‐oxide ceramic matrix composites (CMCs) with and without monazite (LaPO₄) fiber‐matrix interfaces. Twelve sequential aluminum oxychloride (AlOCl) infiltrations with 1 hour heat treatments at 1100°C and a final 1 hour heat treatment at 1200°C were used for matrix densification. This matrix processing sequence severely degraded CMC mechanical properties. CMC tensile strengths and interlaminar tensile (ILT) strengths were less than 10 MPa and 1 MPa, respectively. Axial fracture of Nextel? 610 fibers was observed after ILT testing, highlighting the extreme degradation of fiber strength. Extensive characterization was done to attempt to determine the responsible degradation mechanisms. Changes in Nextel? 610 fiber microstructure after CMC processing were characterized by optical microscopy, SEM, and extensively by TEM. In AlOCl degraded fibers, grain boundaries near the fiber surface were wetted with a glass that contained Y₂O₃/SiO₂ or Y₂O₃/La₂O₃/P₂O₅/SiO₂, and near‐surface pores were partially filled with Al₂O₃. This glass must also contain some Al₂O₃ and initially some chlorine. AlOCl decomposition products were predicted using the FactSage^® Thermochemical code, and were characterized by mass spectrometry. Effects of AlOCl precursors on monazite coated and uncoated Nextel? 610 fibers tow and filament strength were evaluated. A mechanism for the severe degradation of the oxide‐oxide CMCs and Nextel? 610 fibers that involves subcritical crack growth promoted by release of chlorine containing species during breakdown of intergranular glasses in an anhydrous environment is proposed.     

Controlling Stereoselection in Aza-Cope-Mannich Reactions

The synthesis of 2-substituted cis-octahydroindolones from the reaction of cis-2-amino-1-alkenylcyclopentanols with aldehydes was studied to examine whether stereoselection in the aza-Cope–Mannich reaction could be controlled by the nature of the nitrogen substituent. 2-Alkylamino-1-(1-phenylethenyl)cyclopentanols 7 and 8 , which contain nitrogen substituents of widely differing size (Me and CHPh₂), were condensed with four aldehydes to give oxazolidines 9a–d and 10a-c. Rearrangement of these intermediates at 23–60 °C, in the presence of 0.9 equiv of (±)-10-camphorsulfonic acid in acetonitrile, gave cis-octahydroindolones 11a-d and 12a–c in yields of 77–95%. Using a combination of single-crystal X-ray crystallography, ¹H nOe measurements, and comparisons with known materials it was established that the N-methyl oxazolidines 9a–d provided exclusively cis-octahydroindolones having the 2-substituent trans to the angular substituents, while N-benzhydryl analogs 10a–c provided exclusively the all-cis products 12a–c. These results are interpreted to mean: (1) When the nitrogen substituent is small (Me), the stereochemistry-determining [3,3]-sigmatropic rearrangement occurs preferentially through a transition-state topography having the R² substituent oriented quasiequatorially ( 14 → 15 → 16 ); (2) When this substituent is large (CHPh₂), destabilizing steric interactions between the vicinal R¹ and R² substituents causes the rearrangement to occur preferentially through the alternate iminium ion stereoisomer ( 17 → 18 → 19 ).     

Personalized Targeted Therapy for Lung Cancer

Lung cancer has long been recognized as an extremely heterogeneous disease, since its development is unique in every patient in terms of clinical characterizations, prognosis, response and tolerance to treatment. Personalized medicine refers to the use of markers to predict which patient will most likely benefit from a treatment. In lung cancer, the well-developed epidermal growth factor receptor (EGFR) and the newly emerging EML4-anaplastic lymphoma kinase (ALK) are important therapeutic targets. This review covers the basic mechanism of EGFR and EML4-ALK activation, the predictive biomarkers, the mechanism of resistance, and the current targeted tyrosine kinase inhibitors. The efficacy of EGFR and ALK targeted therapies will be discussed in this review by summarizing the prospective clinical trials, which were performed in biomarker-based selected patients. In addition, the revolutionary sequencing and systems strategies will also be included in this review since these technologies will provide a comprehensive understanding in the molecular characterization of cancer, allow better stratification of patients for the most appropriate targeted therapies, eventually resulting in a more promising personalized treatment. The relatively low incidence of EGFR and ALK in non-Asian patients and the lack of response in mutant patients limit the application of the therapies targeting EGFR or ALK. Nevertheless, it is foreseeable that the sequencing and systems strategies may offer a solution for those patients.     

Subtle variations in the structure of crosslinked epoxy networks and the impact upon mechanical and thermal properties

Presented here is an investigation of the structure–property relationships of crosslinked networks using three bi-functional glycidyl ether aromatic epoxy resins, two bi-aryl and one tri-aryl, cured with bi- and tri-aryl amines. Subtle changes to the monomer chemistry including changing aromatic substitution patterns from meta to para, methylene to isopropyl and isopropyl to ether were explored. Changing an epoxy resin backbone from methylene to isopropyl enhances backbone rigidity thus increasing glass transition temperature (T_g), yield strength, and strain despite reducing modulus. Changing meta-substitution to para increases T_g and yield strain while leaving strength unaffected and reducing modulus. Changing isopropyl linkages to ether reduces modulus, strength, T_g, and yield strain reflecting increased molecular flexibility. Using three instead of two aromatic rings increases the molecular weight between crosslinks thereby decreasing T_g and yield strain while increasing modulus and strength. Despite the complexities of multiple systems for varying epoxy resins and amine hardeners, the effect upon network properties is explained in terms of short- and long-range molecular and segmental mobility, crosslink density, and equilibrium packing density. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48874.     

Analysis and Optimization of a Synthetic Milkweed Floral Attractant for Mosquitoes

A pentane extract of flowers of common milkweed, Asclepias syriaca (Asclepiadaceae), elicited significant orientation from both male and female Culex pipiens in a dual-port flight olfactometer. Analysis of the extract by gas chromatography-mass spectrometry revealed six major constituents in order of relative abundance: benzaldehyde, (E)-β-ocimene, phenylacetaldehyde, benzyl alcohol, nonanal, and (E)-2-nonenal. Although not all were collected from the headspace profile of live flowers, a synthetic blend of these six compounds, when presented to mosquitoes in the same levels and proportions that occur in the extract, elicited a response comparable to the extract. Subtractive behavioral bioassays demonstrated that a three-component blend consisting of benzaldehyde, phenylacetaldehyde, and (E)-2-nonenal was as attractive as the full blend. These findings suggest the potential use of synthetic floral-odor blends for monitoring or control of both male and female disease-vectoring mosquitoes.     

ACOUSTIC STUDIES OF INTERFACIAL EFFECTS IN AIRLIFT REACTORS

Rational design of airlift reactors for the culture of plant and animal cells is impeded by a lack of understanding of the causes of loss of viability. Some recent speculations in the literature suggest that gas-liquid interfacial phenomena have played prominent roles in observed instances of loss of viability in both insect and animal cell cultures. The important interfacial events may include bubble formation and detachment at the sparger, bubble coalescence and breakage, and bubble disengagement at the free surface-entailing film thinning, film rupture, and film droplet ejection.

We have carried out an experimental investigation of interfacial phenomena using macrovideography and acoustic signals recorded at both the sparger and the free surface. Data have been collected for several liquid media including distilled water, distilled water with electrolyte (NaCl), and aqueous solutions of glycerol (μ = 3 to 9.5 cP). The studies were conducted in a 3-liter, acrylic plastic, split-column airlift reactor, and air was introduced through interchangeable sieve plates (with hole diameters of 1, 2, and 3 mm). Time-series data collected from the microphone were processed for mean and root-mean-square values, and Fourier transforms were computed to identify important signal energies. A sequence of experiments was also conducted that was designed to relate specific interfacial phenomena to the frequencies of the noises produced.     

HEAT TRANSFER IN A THIN LIQUID FILM IN THE PRESENCE OF AN ELECTRIC FIELD

Heat transfer enhancement in an evaporating thin liquid film utilizing a electric field under isothermal interfacial condition is presented. A new mathematical model subjected to van der Waals attractive forces, capillary pressure, and an electric field is developed to describe the heat transfer enhancement in the evaporating thin liquid film. The effect of the electrostatic field on the curvature of the thin film, evaporative flux, pressure gradient distribution, heat flux, and heat transfer coefficient in the thin film is presented. The results show that applying an electric field can enhance heat transfer in a thin liquid film significantly. In addition, utilizing electric fields on the evaporating film will be a way to expand the extended meniscus region to attain high heat transfer coefficients and high rates of heat flux.     

The jet shape of concentric mixers

In this paper, we present an analytical and experimental study of the mixing region and jet shape in concentric mixers. Based on a simple but effective analytical model, we are able to predict the growth of the mixing region with respect to downstream distance. An experimental study is conducted on the concentric mixing of paper fibre stock and water. By comparing with experimental results, we confirm that the shape of the mixing region is a practical indicator of mixing efficiency with the consideration of jet velocity and geometry including the nozzle wall thickness.     

Chemistry of the Interface Between Aluminum and Polyester Films

It has been observed that the adhesion between vacuum-evaporated aluminum and poly(ethylene isophthalate-co-ethylene sodium sulfoisophthalate) copolymer is approximately five times greater than the adhesion between vacuum-evaporated aluminum and biaxially-oriented poly(ethylene terephthalate) film. To describe the interface between the aluminum and these polymeric substrates, thermoanalytical, spectroscopic and microscopic techniques have been applied. Definite changes in surface elemental composition and chemical functionality occur upon metallization of the polymer films. Aluminized samples contained two new oxygen functionalities; one due to the aluminum oxide and the other due to an organoaluminum species. Thermal degradation, as may occur during vacuum evaporation, would be expected to yield a carboxylic acid endgroup and a vinyl endgroup for each chain scission reaction that occurred. Reaction of aluminum with these carboxylic acid endgroups is thought to be responsible for the organoaluminum oxygen peak that was observed. Based on the XPS data, however, the level of this new functionality was comparable for both types of polyester film. Thus, this new functionality may be involved in promoting aluminum/polyester adhesion, but by itself cannot explain the differences in the level of adhesion that are attained. It appears, based on the transmission electron micrographs, that the aluminum deposit penetrates the copolymer coating to a greater depth than it does the PET. The greater level of penetration could be responsible for the greater adhesion obtained between vacuum-evaporated aluminum and the copolymer film compared with the level of adhesion obtained with the PET film. Based on this work, it appears that the adhesion of the vacuum-evaporated aluminum to both polyesters has a similar chemical component (type and amount) but a different extent of the mechanical component.     

Comparison of relative viscosity measurement of polyvinylpyrrolidone in water by glass capillary viscometer and differential dual‐capillary viscometer

The relative viscosity (RV) of polyvinylpyrrolidone (PVP) with different molecular weights was measured with a glass capillary viscometer and with a differential dual‐capillary viscometer in water at different concentrations. For the differential dual‐capillary viscometer, RV increases with a decreasing flow rate, especially for high molecular weight PVP at a 1% concentration. A good agreement in the RV between the two methods can be obtained for PVP with different molecular weights and at various concentrations if an appropriate flow rate is selected for the differential dual‐capillary viscometer. Special precaution is needed when using the differential dual‐capillary viscometer to measure the viscosity of a pure solvent. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1312–1315, 2002