Mechanical Properties of Dry-Pressed Ceramic Green Products: The Effect of the Binder

The strength of alumina green samples prepared by uniaxial pressing of powders spray-dried with two binders such as poly(ethylene glycol) or poly(vinyl alcohol) is discussed in terms of (i) the adhesive properties of the polymer-rich external layer of spray-dried granules and (ii) the mechanical properties of this layer. A transition from intra- to intergranular fracture is observed when the glass transition temperature of the binder increases. The influence of the binder on the defect size distribution in the green products is investigated using the classical Weibull statistics.     

Structural and rheological investigation of interphase in polyethylene/polyamide/nanoclay ternary blends

This study aims at investigating and characterizing the interphase in Polyethylene (PE)/Polyamide (PA) blends with nodular morphology, filled with organically modified Montmorillonite (C30B), using structural and rheological experimental techniques. PE/PA/C30B blends have been prepared by simultaneous mixing at a dispersed phase fraction (PE or PA) of 20% and a clay fraction ranging from 1 to 6%. Structural properties of the interphase have been investigated using XRD combined with TEM micrographs. The presence of numerous interphase defects is evidenced, and the effect of interphase disorder is discussed. Linear viscoelastic properties show the contribution of the interphase in PE matrix ternary blends at all clay fractions, whereas interphase effects are masked by the contribution of dispersed nanoclay particles in PA matrix ternary blends.     

Enantioselective Organocatalytic Michael Addition of Cyclobutanones to Nitroalkenes

Synthetic applications of cyclobutanones other than ring expansion and fragmentation reactions are rare. Herein, highly efficient diastereo‐ and enantioselective organocatalytic Michael additions of 2‐substituted cyclobutanone derivatives to nitroalkenes are reported allowing the stereocontrolled creation of ‘all‐carbon’ quaternary centers. The approach relies on both the use of Brønsted base/hydrogen‐bond donor bifunctional organocatalysts, and importantly, the specific stabilization and activation of cyclobutanone with a secondary amide moiety. The reaction was found to nicely accommodate a broad scope of substrates, allowing the control of up to three contiguous stereogenic centers. This work has opened new synthetic opportunities.     

Polystyrene latex particles bearing primary amine groups via soap‐free emulsion polymerization

Polystyrene latexes were prepared in the presence of an amino‐containing functional comonomer, N‐(3‐aminopropyl)methacrylamide hydrochloride (APMH), via soap‐free batch emulsion polymerization initiated by the cationic initiator 2,2′‐azobis(2‐amidinopropane) dihydrochloride. These latexes were characterized by studying the influence of the ionic comonomers on the polymerization kinetics, particle size, surface charge density and colloidal properties. The synthesized latexes were monodisperse with a final size between 100 and 600 nm depending on the APMH concentration. The initial polymerization rate and the particle number increased in accordance with the Smith–Ewart theory for soap‐free styrene emulsion polymerization with a hydrophilic functional comonomer. The final functionalization rate of the particles has been particularly studied with the intention of fitting the prepared latexes to be used in the immobilization of biological molecules for biological sample preparation and diagnostic applications. © 2020 Society of Chemical Industry     

Analysis of the Single-Crystalline Silicon Photovoltaic (PV) Module Performances Under Low γ - Radiation from Radioactive Source

The present paper is about an experimental evaluation of the terrestrial silicon single-crystalline solar PV module behavior under low gamma radiation. The     

From Oxadiazole to Triazole Analogues: Optimization toward a Dual Orexin Receptor Antagonist with Improved in vivo Efficacy in Dogs

The orexin system is responsible for regulating the sleep-wake cycle. Suvorexant, a dual orexin receptor antagonist (DORA) is approved by the FDA for the treatment of insomnia disorders. Herein, we report the optimization efforts toward a DORA, where our starting point was (5-methoxy-4-methyl-2-[1,2,3]triazol-2-yl-phenyl)-{(S)-2-[5-(2-trifluoromethoxy-phenyl)-[1,2,4]oxadiazol-3-yl]-pyrrolidin-1-yl}methanone ( 6 ), a compound which emerged from our in-house research program. Compound 6 was shown to be a potent, brain-penetrating DORA with in vivo efficacy similar to suvorexant in rats. However, shortcomings from low metabolic stability, high plasma protein binding (PPB), low brain free fraction (f_u brain), and low aqueous solubility, were identified and hence, compound 6 was not an ideal candidate for further development. Our optimization efforts addressing the above-mentioned shortcomings resulted in the identification of (4-chloro-2-[1,2,3]triazol-2-yl-phenyl)-{(S)-2-methyl-2-[5-(2-trifluoromethoxy-phenyl)-4H-[1,2,4]triazol-3-yl]-pyrrolidin-1-yl}l-methanone ( 42 ), a DORA with improved in vivo efficacy compared to 6 .     

Mixture-proportioning of high-performance concrete

The paper presents a new approach to design concrete mixtures. It is based upon a set of models relating composition and engineering properties of concrete, to be implemented into software, linked with a material database. The principles underlying the various models are summarized, most of which focus on the granular structure of fresh/hardened concrete. A global approach to concrete is promoted, where performance specifications can be formulated in terms of fresh concrete (yield stress, plastic viscosity, slump and air content), hardening concrete (adiabatic temperature rise and autogenous shrinkage) and hardened concrete (compressive strength at any age, tensile strength, elastic modulus, creep and shrinkage). This approach is illustrated through the design of a special high-shrinkage high-performance concrete (HPC) for road application. To date, durability is lacking in the model and requires further research.     

Comparison of the wound-activated transformation of caulerpenyne by invasive and noninvasive Caulerpa species of the Mediterranean

The invasive green alga, Caulerpa taxifolia, that has spread rapidly after its introduction into the Mediterranean and the North American Pacific, reacts to wounding by transforming its major metabolite caulerpenyne (1). This wound-activated reaction involves the transformation of the bis-enol acetate moiety of 1, releasing reactive 1,4-dialdehydes. The ability to perform this transformation is found also in both the noninvasive Mediterranean C. prolifera and the invasive C. racemosa. Trapping experiments, as well as transformation of the model substrate geranyl acetate, suggest that all three investigated Caulerpa spp. rely on esterases that act upon wounding of the algae by subsequently removing the three acetate residues of caulerpenyne. The resulting reactive 1,4-dialdehyde oxytoxin 2 (9) can be identified by liquid chromatography–mass spectrometry and is unstable in the wounded tissue. Caulerpenyne transformation occurs rapidly, and severe tissue damage caused degradation of more than 50% of the stored caulerpenyne within 1 min in all three algae. Prevention of the enzymatic reaction before extraction, by shock freezing the tissue with liquid nitrogen, was used for the determination of the caulerpenyne content in intact algae. It gives about twofold higher values compared to an established methanol extraction protocol. The speed and mechanism of the wound-activated transformation, as well as the caulerpenyne content in intact tissue of invasive and noninvasive Caulerpa spp., are comparable. Thus, this enzymatic , transformation, despite being fast and efficient, is likely not the key for the success of the investigated invasive species.     

Chitosan supported palladium catalyst. VI. Nitroaniline degradation

A chitosan‐supported palladium catalyst was prepared by immobilization of palladium on glutaraldehyde crosslinked chitosan followed by in situ chemical reduction. This catalyst was successfully used for the degradation of 4‐nitroaniline (4‐NA) in the presence of sodium formate, used as the hydrogen donor. The reaction product was 1,4‐phenylenediamine. The degradation was favored by acidic pH. A 10 to 15 excess of formate (compared to 4‐NA) is required to achieve complete degradation of the substrate. The reaction appears to be limited to the external layers of the catalyst: small particle size is required to optimize the degradation kinetics. Alternatively, an increase of catalyst dosage is required to increase kinetic rates but at the expense of palladium consumption. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1634–1642, 2004     

New alginate foams: Box‐Behnken design of their manufacturing; fire retardant and thermal insulating properties

A new method for preparing alginate foams with progressive release of copper in the presence of sodium lauryl sulfate (SLS, foaming agent) has been designed. Copper acts as the ionotropic gelling agent through the reaction of copper carbonate with gluconolactone. The process does not require freeze‐drying contrarily to the conventional method used for preparing macroporous alginate foams. The new materials investigated in this study have remarkable thermal properties, including thermal conductivity lower than 0.041 W m^?1 K^?1 and low heat release (below 2 kJ g^?1), which allows labeling these foams self‐extinguishing materials. An experimental design methodology, based on a Box‐Behnken plan with three parameters and three levels, is successfully used for evaluating the impact of the amounts of alginate, SLS, and copper carbonate on the productivity, apparent density, and shrinking at air‐drying. It yielded an optimization of the process for the manufacturing of light, and stable/rigid insulating and thermally stable materials. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45868.