Fracture toughness, strength, and other characteristics of yttria-stabilized zirconium ceramics

The mechanical behavior of zirconium ceramics with different porosities (456 and 1330 MPa) is studied with an accent on the fracture toughness (the study of other characteristics in a wide temperature range plays an auxiliary role) The tests are predominantly performed with the use of a Vickers pyramid (theIF andIS methods) and under flexure (theSEVNB andSENB methods) The results of the indentation and subsequent bending of the specimens are used to plot aR-curve that turns out to be plane It is shown that despite the substantial difference in the strength of the studied variants of ceramics their crack resistance differs inconsiderably The values of the critical coefficients of stress intensity determined by various methods for the same ceramics are shown to differ The results obtained are analyzed using the data of a micro-Raman analysis The tests for crack resistance by the method ofSEVNB (bending of a beam with a polishedV-notch) show that the specimens do not undergo a tetragonal-monoclinic phase transformation during the deposition of a stress concentrator Transleted from Ogneupory i Technicheskaya Keramika, No. 8, pp. 7 – 13, August, 2000.     

Nanofiltration of Magnesium Chloride,Sodium Carbonate,and Calcium Sulphate in Salt Solutions

Abstract

Nanofiltration (NF) membranes have been employed in pre‐treatment unit operations in both thermal and membrane seawater desalination processes. This has resulted in reduction of chemicals used in pretreatment processes as well as lowering the energy consumption and water production cost and, therefore, has led to a more environmentally friendly processes. In order to predict NF membrane performance, a systematic study on the filtration performance of selected commercial NF membranes against brackish water and seawater is required. In this study, three commercial nanofiltration membranes (NF90, NF270, N30F) have been used to treat highly concentrated different salts solutions (MgCl₂, Na₂CO₃, and CaSO₄) at salinity level similar to that of brackish water and seawater. The main parameters studied in this paper are salt concentration and feed pressure. The experimental data were correlated and analysed using the Spiegler‐Kedem model. In particular, the reflection coefficient (σ) of all studied membranes and the solute permeability (P_s) have been determined for all membranes and at different salinity levels of studied salts. All the studied membranes fitted the model well for all investigated salts except the experimental data of MgCl₂ using N30F membrane, which did not fit well at low rejection. The results showed that NF90 produced a high rejection around 97% for all salts with medium permeate flux while NF270 gave a high flux with medium rejection and N30F gave low rejection and flux.     

Kinetics, energy characteristics, and intensification of crystallization processes in chemical precipitation of hardness ions

An analysis of the literature data on the solubility and kinetics of the chemical (reagent) precipitation of calcium carbonate and magnesium hydroxide is performed. The possible causes of the significant discrepancy in the available data are considered. The kinetics of the homogeneous and heterogeneous crystallization of calcium carbonate and magnesium hydroxide in reagent precipitation is studied using different methods. It is shown that the use of heterogeneous crystallization on seed particles pretreated in an ultrasonic field raises the rate of crystallization by an order of magnitude. The kinetics of nucleation is studied; the effect of supersaturation and temperature on the induction period in the homogeneous and heterogeneous nucleation of CaCO₃ and Mg(OH)₂ crystals is investigated. The energy characteristics of nucleation, namely, the interfacial tension (surface energy) and activation energy, are determined. The use of fine-dispersed particles activated by ultrasound makes it possible to considerably reduce the energy barrier for nucleation.     

Theranostic Platforms Based on Silica and Magnetic Nanoparticles Containing Quinacrine,Chitosan, Fluorophores,and Quantum Dots

In this paper, we describe the synthesis of multilayer nanoparticles as a platform for the diagnosis and treatment of ischemic injuries. The platform is based on magnetite (MNP) and silica (SNP) nanoparticles, while quinacrine is used as an anti-ischemic agent. The synthesis includes the surface modification of nanoparticles with (3-glycidyloxypropyl)trimethoxysilane (GPMS), the immobilization of quinacrine, and the formation of a chitosan coating, which is used to fix the fluorophore indocyanine green (ICG) and colloidal quantum dots AgInS₂/ZnS (CQDs), which serve as secondary radiation sources. The potential theranostic platform was studied in laboratory animals.     

Degradation and Metabolite Profiling of Benz (a) Anthracene,Dibenz (a,h) Anthracene and Indeno [1, 2, 3-cd] Pyrene by Aspergillus terricola

Mycoremediation of low molecular weight polycyclic aromatic hydrocarbons (PAH) is well studied. This study highlights the degradation of high molecular weight PAH (HMW-PAHs): Benz (a) anthracene (BAA), Dibenz (a, h) anthracene (DBA), and Indeno pyrene (IND) by Aspergillus terricola var americanus. The metabolism of the HMW-PAHs by this fungus was investigated in liquid submerged culture added with 60 mg/L of each compound. Depletion of BAA, DBA, and IND was 94.80, 90.16, and 93.80%, respectively, after 10 days of culture. Fungal broth solvent extracts were analyzed for the presence of metabolites by gas chromatography mass spectrometry and the extracellular enzymes produced were also assayed. The coexistence of two metabolic pathways, cytochrome P450 monooxygenase and ligninolytic pathway were identified. A high laccase activity was observed in BAA cultures on day 4 when compared to other PAH's studied. In conclusion, A. terricola might be a promising fungus for bioremediation of HMW-PAH mixtures co-metabolically.     

Impact of the Zr-substitution on phase composition,structure, magnetic,and microwave properties of the BaM hexaferrite

Rapid developments in information technologies and a large rise in electrical and electronic equipment have generated different forms of electronic environmental contamination. Microwave absorption materials are important to avoid the damage that can be caused by electromagnetic radiation. A necessary condition for the absorption of the most incoming radiation is balanced wave impedance at the air/shield interface, which depends on the studied materials' magnetic and electrical properties. The paper introduces the preparation of BaFe_12-xZr_xO₁₉ (x = 0.1, 0.3, 0.6, 0.9, and 1.2) using a solid-state reaction technique. The studied samples were examined by X-ray diffraction, scanning electron microscopy, vibrating sample magnetometer, and a vector network analyzer. The studied samples showed that controlling the grain size and the prepared samples' magnetic properties play an important role in enhancing the microwave radiation absorption. The examined samples can be a promising absorption material in electromagnetic shielding applications.     

Crosslinking of poly(vinyl chloride) with metal oxides,sulfur, and organo sulfur compounds

The crosslinking of poly(vinyl chloride) in the presence of zinc oxide, magnesium oxide, ethylenethiourea (ETU), tetramethylthiuramdisulfide (TMTD), and sulfur at 160 and 180°C has been studied. The effects of ETU and sulfur on the crosslinking of PVC in the presence of TMTD have been individually studied. It has been found that zinc dimethyldivhiocarbamate (ZnDMDC) is the actual crosslinking agent and heat stabilizer of PVC, formed in the cured polymer mix.     

Coumarin-Rasagiline Hybrids as Potent and Selective hMAO-B Inhibitors,Antioxidants, and Neuroprotective Agents

The frequency, complexity and morbidity of neurodegenerative diseases make them a great challenge for nowadays medicine. Most of the treatments currently used for Parkinson's disease – the second most prevalent – are only symptomatic. Therefore, it is urgent to develop drugs that are able to act simultaneously on different targets, being able to stop neuronal death and promote the recovery of neuronal populations already affected. In this work, we studied the activity of a series of hybrid molecules, which combine the structure of both coumarin and an alkynylamine group inspired on rasagiline, as MAO inhibitors, antioxidants and neuroprotective agents. Half of the studied hybrids turned out to be selective monoamine oxidase B (hMAO-B) inhibitors in the low micro/nanomolar range, demonstrating that positions 3 (compounds 1–3 ) and 7 (compounds 8 and 10 ) of the coumarin scaffold are the most suitable for the incorporation of the alkynylamine chain. All the studied compounds proved to be capable of neutralizing free radicals (DPPH). Finally, the 4-(but-2-yn-1-ylamino)coumarin ( 5 ) showed neuroprotective effects on glial cells and the 4-methyl-7-(pent-2-yn-1-ylamino)coumarin ( 8 ) inhibited intraneuronal ROS production as well.     

Fatty Acids,Tocopherols, Tocotrienols,Phytosterols, Carotenoids,and Squalene in Seed Oils of Hyptis suaveolens,Leonotis nepetifolia,and Ocimum sanctum

The oil yield and composition of fatty acids, tocopherols, tocotrienols, sterols, carotenoids, and squalene in the seeds of three species—Hyptis suaveolens, Leonotis nepetifolia, Ocimum sanctum—belonging to the Lamiaceae family, are studied. The oil yields are 12.1%, 16.1%, and 29.0% in O. sanctum, H. suaveolens, and L. nepetifolia, respectively. The unsaturated fatty acids are a predominant group (86.8–92.1%) in all three investigated plants; however, the profile for each species is unique. The main fatty acid differs as follows: H. suaveolens—linoleic acid (85.8%), L. nepetifolia—oleic acid (58.3%), and O. sanctum—α‐linolenic (48.6%). γ‐Tocopherol accounts for over 97%, 90%, and 93% of the total tocochromanol content (sum of tocopherols and tocotrienols) in H. suaveolens, L. nepetifolia, and O. sanctum, respectively. Two tocotrienol homologues, α and γ, are detected only in L. nepetifolia. β‐Sitosterol is the main detected sterol (38–59%) in all three species. High levels of campesterol (18–20%), Δ5‐stigmasterol (9–21%), and Δ5‐avenasterol (7–12%) are also detected. Squalene is detected only in O. sanctum (45.8 mg/100 g oil). The content of sterols, tocochromanols, and carotenoids in the investigated Lamiaceae plant seed oils ranges between 279.5–576.3, 54.5–66.7, and 0.3–3.1 mg/100 g oil, respectively. Practical Applications: Lamiaceae plants are of medicinal interest due to the presence of a broad spectrum of bioactive molecules. The present study demonstrates that seeds of the species H. suaveolens, L. nepetifolia, and O. sanctum are rich sources of bioactive compounds of lipophilic nature. There is limited knowledge associated with the composition of tocopherols, tocotrienols, sterols, carotenoids, and squalene. The results of the studied medicinal plants may enhance future targeted applications in various sectors.     

Synthesis, characterization, and properties of an efficient and selective adsorbent to mercury (II)

The synthesis of a water-insoluble adsorbent resin was carried out by radical polymerization of [2-(methacryloyloxy)ethyl] trimethyl ammonium chloride by using ammonium peroxydisulfate as initiator and N,N′-methylene-bis-acrylamide (MBA) as crosslinking reagent. The adsorbent was characterized by elemental analyses, and FT-IR spectroscopy. The thermal stability was studied in the presence of Hg(II). The ability to bind Hg(II), Cd(II), Zn(II), Pb(II), Cu(II), Cr(III), and U(VI) as well as the maximum adsorption capacity, and elution of the Hg(II) from the loaded resin was studied. At pH 2 the adsorbent retained 95% of Hg(II) from an aqueous solution containing 1 g/L in Hg(II). The retention of other metal ions was lower than 15%. Sorption selectivity from the binary mixtures Hg(II)-Cd(II), Hg(II)-Zn(II), Hg(II)-Pb(II), and Hg(II)-Cr(III) was studied at the optimum sorption pH value. Received: 20 April 1997/Revised: 24 July 1997/Accepted: 6 August 1997     

Removal of Cupric Ions by Means of Activated Sludge: Kinetics,Isotherms, and Yields

Abstract

Adsorption of Cu(II) on activated sludge from the treatment of municipal sewage is studied. The resulting adsorption isotherm is of the Langmuir type.     

Effect of organoclay on the morphology,mechanical, thermal,and rheological properties of organophilic montmorillonite nanoclay based thermoplastic polyurethane nanocomposites prepared by melt blending

Polymer nanocomposites based on the thermoplastic polyurethane (TPU) and organically modified montmorillonite (OMMT) was prepared by melt intercalation technique using a laboratory internal batch mixer followed by compression molding. Varying amount of organically modified nanoclays (1, 3, 5, 7, and 9 wt%) was added to the TPU matrix to examine the influence of organoclay on nanophase morphology and structure–property relationships. The interaction between TPU matrix and nanofiller was studied by infrared spectroscopy. The morphology of nanocomposites was studied by X‐ray diffraction, transmission electron microscopy, and atomic force microscopy that shows melt mixing by a batch mixer is an effective method for dispersing OMMT throughout the TPU matrix. Thermogravimetric analysis revealed that incorporation of organoclay enhances the thermal stability of the nanocomposites significantly. Differential scanning calorimetry was employed to measure the melting point and glass transition temperature (T_g) of soft segments. The reinforcing effect of the organoclay was determined by dynamic mechanical analysis and physico–mechanical testing. The effects of nanoclay concentration and processing parameters on the dynamic viscoelastic properties of the nanocomposites were studied by a rubber process analyzer using frequency sweep. A significant increase in the viscosity and storage modulus of the nanocomposites was found with the increasing clay content. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers     

Structural changes of regenerated cellulose dissolved in FeTNa,NaOH/thiourea,and NMMO systems

Regenerated cellulose was prepared from microcrystalline cellulose (MCC) via dissolution in three well‐known nonderivatizing systems: ferric chloride/sodium tartarate/sodium hydroxide (FeTNa), sodium hydroxide/thiourea (NaOH/thiourea), and N‐methylmorpholine‐N‐oxide (NMMO) systems. The effect of regeneration using the different systems on the supramolecular structure of the regenerated celluloses was studied using X‐ray diffraction and Fourier transform infrared (FTIR). The effect of regeneration on supermolecular structure, morphology, and thermal stability of regenerated celluloses were studied using scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). The effect of regeneration systems used on the chemical reactivity of cellulose toward carboxymethylation, acetylation, and cyanoethylation reactions was briefly studied. The results showed dependence of all the aforementioned properties on the dissolution reagent used in spite of that all studied reagents cause the same change in cellulose crystalline structure (from cellulose I to cellulose II). The degree of polymerization, crystallinity, and thermal stability of the regenerated cellulose (RC) samples were in the following order: NaOH/thiourea RC > FeTNa RC > NMMO RC. SEM micrograph showed unique surface for the NMMO RC sample. The reactivity of the different regenerated cellulose samples toward carboxymethylation, cyanoethylation, and acetylation depended mainly on the reaction system and conditions used rather than on crystallinity of regenerated cellulose. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Antimony polymers,part 2. Physical,chemical and thermal properties

Three antimony-containing polymers (P₁, P₂, P₃) were synthesized by reacting triphenyl antimony dinitrate with bisphenol A (P₁), with tetrabromobisphenol A (P₂) and with N,N′-bis(4-hydroxybenzylidene)-oxydianiline (P₃). Solubility, density, chemical and thermal stability of these antimony polymers have been evaluated. The polymers are only soluble in dipolar aprotic solvents like dimethyl sulfoxide, dimethylformamide, dimethylacetamide, etc., and have relatively high densities (1.2–1.8 g cm^–3). The solubility parameters (δ) and chemical stability of the polymers were studied in different chemical environments. The thermal properties of the polymers have been studied by thermogravimetric analysis, differential thermal analysis and isothermal gravimetric analysis.     

Preparation,Characterization, and Adsorption Properties of Amino-Alky Cellulose for 2, 4, 6-Trinitrotoluene

A novel adsorbent, amino-alky cellulose (AmAC), is prepared by chlorination and amination of hydroxyethyl cellulose (HEC). AmAC are characterized by ¹³C-NMR and used as adsorbent to remove 2, 4, 6-trinitrotoluene (TNT) from waste water. Effects of various parameters including solvent and amine group content are studied. Adsorption mechanisms are also analyzed. Results show that the maximum adsorption capacity is 69.23 mg g^?1 and removal efficiency of 99.30%, while the adsorption deeds are attributed to the hydrogen bond between TNT molecules and amino-alky cellulose. The equilibrium sorption is well demonstrated by Freundlich isotherm model. The reusability experiment shows the adsorbed TNT could be desorbed by ethanol eluant when the pH is 1.     

Physicochemical, mineralogical, and morphological characteristics of concrete exposed to elevated temperatures

Concrete cubes prepared from ordinary Portland cement (OPC) of known chemical, mineralogical, and physical performance characteristics and fired to various temperature regimes up to 1000 °C in steps of 100 °C for a constant period of 5 h have been studied by using X-ray diffraction (XRD) and DTA/TGA to establish the effect of elevated temperatures on the mineralogical changes occurring in the hydrated phases of concrete. The changes in physical state of concrete were studied by measuring ultrasonic pulse velocity (UPV) and consequent deterioration in the compressive strength with increase in temperature. Scanning electron microscopy (SEM) studies showed distinct morphological changes corresponding to deterioration of concrete exposed to higher temperatures.     

An ab initio study on properties of cationic chalcogen bonds in XF2Y+⋯NCZ (X═H,CN, F; Y═S,Se; Z═H,Cl, Br) complexes

The geometries, interaction energies, and bonding properties of cationic chalcogen bonds are studied in binary complexes XF₂Y⁺?NCZ (X═H, CN, F; Y═S, Se; Z═H, Cl, Br). The nature of these interactions is studied by a vast number of methods, including molecular electrostatic potential (MEP), Noncovalent Interaction Index (NCI), quantum theory of atoms in molecules (QTAIM), and natural bond orbital (NBO) analyses. The interaction energies of these complexes vary between ?20.94?kcal/mol in HF₂S⁺?NCH and ?33.72?kcal/mol in F₃Se⁺?NCBr. According to the QTAIM analysis, all these cationic chalcogen bonds are classified as a closed-shell interaction with a partial covalent character. Moreover, cooperative effects between cationic chalcogen bond and hydrogen or halogen bond interactions are studied in ternary XF₂Y⁺?NCZ?NH₃ complexes. These cooperative effects are analyzed in terms of the parameters derived from the QTAIM and NBO analyses, and electron density difference plots.     

Elasticity,hardness, and thermal properties of ZrBn (n=1, 2, 12)

Elasticity, hardness, and thermal conductivity of ZrBn (n=1, 2, 12) were studied in this paper by using the first-principles calculations of plane wave ultra-soft pseudo-potential technology based on the density functional theory (DFT). Deep analysis of elasticity and anisotropy was carried out, indicating that ZrB and ZrB₂ are soft (the most anisotropic) and superhard (the least anisotropic) respectively. The transverse wave speed (V_t), longitudinal wave speed (V_l) and the minimum thermal conductivity κ_min (both Clark and Cahill model) were calculated. Our investigations show that ZrB is a good heat insulating material and a good lubricant, ZrB₁₂ can be served as a good high-temperature-resistant material and superconducting material, and ZrB₂ is a good wear-resistant material.     

A methacrylate monomer bearing nitro,aryl, and hydroxyl side groups: Homopolymerization,characterization, dielectric,and thermal degradation behaviors

2‐Hydroxy‐3‐(4‐nitrophenoxy)propyl methacrylate (HNPPMA) monomer was synthesized. The poly(HNPPMA) was prepared by free radical polymerization (FRP) method. The characterization of poly(HNPPMA) was carried out using FT‐IR, NMR, differential scanning calorimetry, and GPC techniques. The thermal stability and degradation behavior of this polymer have been studied by using thermogravimetry (TG), GC‐MS, NMR, and FT‐IR. The results were in comparison to poly[2‐hydroxy‐3‐(1‐naphtyloxy)propyl methacrylate] sample with α‐naphtyloxy side group prepared by the same method in the our previous study. The effect of thermal activation on non‐isothermal decomposition kinetics of poly(HNPPMA) was investigated using thermogravimetric analysis according to Flynn‐Wall‐Ozawa method. The dielectric measurements of poly(HNPPMA) and doped with europium(III)chloride (EuCI₃) were investigated by impedance analyzer technique in range of 10–4000 Hz frequency by depending on the alternating current conductivities. The mode of thermal degradation including formation of the main products of poly(HNPPMA) degraded from ambient temperature to 500 °C was identified. S°, the cold ring fraction (CRF) was collected from room temperature to 500 °C. The structure of the degradation products has also been studied depending on the GC‐MS analysis. The thermal degradation mechanism for poly(HNPPMA) with radical degradation processes thought to dominate at high temperature was proposed based on GC/MS, NMR, FT‐IR, and taking into account the new products and differences in stability. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43925.     

Crystallization,melting behavior,and morphology of BPP/HDPE blend

The crystallization, melting behavior, and morphology of a low ethylene content block propylene–ethylene copolymer (BPP) and a high-density polyethylene (HDPE) blend were studied. It was found that the existence of ethylene–propylene rubber (EPR) in BPP has more influence on the crystallization of HDPE than on that of PP. This leads to the decreasing of the melting temperature of the HDPE component in the blends. It is suggested that the EPR component in BPP shifted to the HDPE component during the blending process. The crystallinity of the HDPE phase in the blends decreased with increasing BPP content. The morphology of these blends was studied by polarized light microscopy (PLM) and SEM. For a BPP-rich blend, it was observed that the HDPE phase formed particles dispersed in the PP matrix. The amorphous EPR chains may penetrate into HDPE particles to form a transition layer. © 1998 John Wiley & Sons, Inc. J. Appl. Polym. Sci. 69: 2469–2475, 1998