Inference about long run canonical correlations

This article proposes methods for testing the null hypothesis that a number of so‐called long run canonical correlations (LRCCs) are zero. Two test statistics are proposed and their limiting distributions are derived under the null hypothesis. The finite sample properties of the tests are illustrated via a number of simulation studies that reveal the asymptotic theory provides a good guidance to behaviour in moderate or large sized samples. It is shown that the statistics provide a natural way for testing the asymptotic independence of two standardized sums. The usefulness of the tests is illustrated via the following examples: inference about cointegrating vector in a particular cointegration model; inference about break points in a cointegration model; moment estimation; parameter estimation in Generalized Method of Moments estimation.     

Interaction of Cucurbit[7]uril with Oxime K027, Atropine,and Paraoxon: Risky or Advantageous Delivery System?

Antidotes against organophosphates often possess physicochemical properties that mitigate their passage across the blood–brain barrier. Cucurbit[7]urils may be successfully used as a drug delivery system for bisquaternary oximes and improve central nervous system targeting. The main aim of these studies was to elucidate the relationship between cucurbit[7]uril, oxime K027, atropine, and paraoxon to define potential risks or advantages of this delivery system in a complex in vivo system. For this reason, in silico (molecular docking combined with umbrella sampling simulation) and in vivo (UHPLC—pharmacokinetics, toxicokinetics; acetylcholinesterase reactivation and functional observatory battery) methods were used. Based on our results, cucurbit[7]urils affect multiple factors in organophosphates poisoning and its therapy by (i) scavenging paraoxon and preventing free fraction of this toxin from entering the brain, (ii) enhancing the availability of atropine in the central nervous system and by (iii) increasing oxime passage into the brain. In conclusion, using cucurbit[7]urils with oximes might positively impact the overall treatment effectiveness and the benefits can outweigh the potential risks.     

Solubility parameter estimation and phase inversion modeling of bentonite-doped polymeric membrane systems

Effects of bentonite concentration on morphology and permeation characteristics of bentonite-doped polysulfone membranes were investigated. Solubility sphere for bentonite was constructed to estimate its solubility parameter. Thermodynamic modeling of phase inversion of this system was carried out using Flory–Huggins theory. The trade-off between thermodynamic and kinetic parameters was used to predict the membrane morphology for bentonite concentration varying from 0 to 5 wt %. The porosity of bentonite-doped membranes decreased up to 3 wt % that increased thereafter. Morphological analysis showed dense cross section with finger-like macrovoids at 3 wt % beyond which it changed to honeycomb structure with large circular voids. Permeability of 3 wt % membrane was the lowest (5.6 × 10⁻¹² m/Pa s) with 95% bovine serum albumin rejection. Contact angle of the membranes decreased from 83 to 66° with bentonite addition making the membrane more hydrophilic. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48450.     

Effect of Porosity on Structure,Young's Modulus,and Thermal Conductivity of SiC Foams by Direct Foaming and Gelcasting

The study demonstrates the aqueous processing of solid‐state‐sintered SiC foams by gelcasting technique. Aside from increasing strength of green bodies, gelcasting monomers were the source of carbon additive which helped in sintering of SiC foams. Sintered foams with the relative density (RD) between 0.44 and 0.11 were processed by direct foaming of SiC slurries followed by gelcasting and sintering. Structural analysis by X‐ray tomography showed the presence of spherical pores with bimodal pore size distribution and the proportion of large size cell and their interconnectivity increased in low RD foams. SEM study revealed that decreased RD resulted in gradual changes in the strut microstructure from the grains with faceted interface to smooth interfaced grains. The analysis of changes in Young's modulus and thermal conductivity with RD were in agreement with the Ashby model for open cell foams.     

Novel organic–inorganic composite material as a cation exchanger from a triterpenoidal system of dammar gum: synthesis,characterization and application

A pioneer study has been conducted to synthesize novel hydrogel starting from a non-cellulosic raw material, gum dammar-a triterpenoidal system, and then converting this hydrogel into an organic–inorganic composite zirconium-based ion exchanger. Gum dammar was cross-linked with polyacrylamide zirconium (IV) iodo-oxalate [Gd-cl-poly(AAm)-Zr (IV) iodo-oxalate] by incorporating inorganic precipitates into the polymeric mixture. The polymeric mixture was synthesized using gum dammar (Gd), acrylamide (AAm), N, N′-methylene-bis-acrylamide (MBA) and potassium persulphate (KPS). The reaction conditions for synthesis of hydrogel and ion exchanger such as time (120 min), temperature (70 °C), solvent (4 mL), concentration of monomer (12.97 × 10^?3 mol/L), initiator (1.48 × 10^?4 mol/L), cross-linker (4.22 × 10^?4 mol/L) and ratio of zirconium oxychloride (0.1 M), potassium iodate (0.1 M) and oxalic acid (0.1 M) in ratio 2:3:2 were optimized to obtain maximum ion exchange capacity (2.02 meq/g). The morphology and structure of hydrogel and ion exchanger were studied using FTIR, SEM, XRD and TGA/DTA/DTG. The SEM study was followed by energy dispersive spectroscopy for elemental analysis. The ion exchanger was quite stable in various acids and bases at low concentration but it completely dissolved in acids and bases at high concentrations. Distribution studies showed that the synthesized ion exchanger had high selectivity for Pb²⁺ ions. Thus, the polymeric-inorganic hybrid material showed integration of both inorganic and organic characteristics within the composite material.     

Titania supported Co-Mn-Al oxide catalysts in total oxidation of ethanol

Catalytic activity of the Co-Mn-Al mixed oxide catalysts (Co:Mn:Al molar ratio of 4:1:1) supported over titania was examined in total oxidation of ethanol. The prepared catalysts were characterized by chemical analysis (AAS), surface area measurements, and temperature programmed techniques (TPR, TPD). In ethanol oxidation, the catalysts activity gradually increased with increasing active phase content. Low concentration of Co-Mn-Al oxides in the catalyst negatively affected formation of reaction byproducts: carbon monoxide production steeply increased when Co + Mn metals concentration were lower than 5 wt.%. On the other hand, formation of the second main reaction intermediate, acetaldehyde was limited, when acidity of the catalyst was not high, i.e. concentration of Co-Mn metals over titania was low.     

Fluorine containing self‐crosslinking acrylic latexes with reduced flammability and their application as polymer binders for heterogeneous cation‐exchange membranes

In this study, self‐crosslinking core–shell latexes comprising copolymerized perfluorethyl groups and a novel flame retardant based on phosphazene derivative were prepared by the semi‐continuous non‐seeded emulsion polymerization of 2,2,2‐trifluorethyl methacrylate, methyl methacrylate, butyl acrylate, methacrylic acid, and hexaallylamino‐cyclo‐triphosphazene as main monomers. For interfacial crosslinking, diacetone acrylamide was copolymerized into the shell layer of latex particles to provide sites for subsequent reaction with adipic acid dihydrazide. The heterogeneous cation‐exchange membranes were obtained by dispersing commercial strong acid cation‐exchange resin powder in the latex binder and casting the mixture followed by keto‐hydrazide crosslinking reaction. It was found that the increased concentration of fluorine atoms and phosphazene units in the macromolecular structure of interfacially crosslinked emulsion polymers resulted in a significant enhancement of their flame resistance and shape stability in aqueous environment. Moreover, the easily prepared heterogeneous cation‐exchange membranes based on latexes with higher amounts of fluorine and phosphazene units were shown to exhibit satisfactory physicochemical and electrochemical properties. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45467.     

3D Coordination Network of Ag(I) Ions with μ 3 -Bridging Melamine Ligands

Abstract  

A new 3D silver complex [Ag(mela)(H₂O)(NO₃)]_n (1) (mela = melamine or 2,4,6-triaminotriazine) is synthesized and characterized by single crystal X-ray diffraction, IR, and elemental analysis. The structural characterization shows that the compound crystallizes in space group C c, a = 8.181(2), b = 10.269(3) c = 11.347(3) ?, β = 105.88(2)°, Z = 4. Out of several structurally characterized transition metal compounds comprising melamine, the titled complex represents a rare example of μ ₃ -melamine coordination mode realized through the heterocycle nitrogen donors. The fluorescent property of complex 1 was investigated and the mechanism was validated by means of a density functional theory (DFT) calculation.     

Separation of Trimethyl Borate from a Liquid Mixture by Pervaporation

Four commercial polyvinyl alcohol (PVA) and polydimethylsiloxane (PDMS) membranes were applied to the pervaporation of an azeotropic mixture containing trimethyl borate, a precursor to boronic acids used in Suzuki couplings and a gaseous anti‐oxidant in solder flux or brazing. The degree of cross‐linking of the chains in the active layer played a crucial role in the membrane process using the membranes PERVAP 4155‐80, PERVAP 4155‐40 and PERVAP 4155‐30. PERVAP 4155‐30 reached the best results from all tested membranes; an impressive selectivity with fast permeation was also achieved with the PERVAP 4060 membrane. Methanol preferentially passed through PERVAP 4155‐30, but trimethyl borate was favorably pervaporated from the mixture by PERVAP 6040, due to the diverse affinities of the membranes.     

Optical and electrical transport properties of polyaniline–silver nanocomposite

Polyaniline–silver nanocomposite has been synthesized successfully by the chemical oxidative polymerization of aniline with ammonium peroxydisulphate as an initiator in presence of negatively charged silver nanoparticles. Silver nanoparticles are prepared by standard citrate reduction method. TEM, SEM, XRD, FTIR, TGA, DSC, optical absorption and photoluminescence studies are done for the morphological, structural, thermal and optical characterization of the polyaniline nanocomposite. From the TEM and SEM image, it is observed that nanoparticles are well dispersed in the polyaniline matrix. XRD pattern shows that polyaniline is amorphous, but peaks present in XRD pattern in polymer nanocomposites are for silver nanoparticles. TGA and DSC results show that polyaniline silver nanocomposite is more crystalline and more thermally stable. A surface plasmon absorption band is obtained from the optical absorption at 380 nm, which indicates that silver nanoparticles are present in the polyaniline matrix. The optical band gap of nanocomposite decreases with increasing content of silver nanoparticles. An enhancement in photoluminescence has been observed in polyaniline–silver nanocomposite than that in pure polyaniline. The electrical conductivity of polyaniline–silver nanocomposite increases with increase in silver nanoparticle content than that of pure polyaniline. This is a simple way by which optical and electrical properties of polyaniline may be enhanced by doping with suitable nanoparticles.