Physicomechanical properties of sibirfom,a porous building material from zeolite-containing rock

The results of experiments on the use of zeolite-containing rock in the production of sibirform, i.e., a foam-glass porous building material, are presented. The main physicomechanical properties of sibirfom are described. It is shown that the microstructure and the properties of the material depend on the chemical and mineral composition of the rock.Translated from Steklo i Keramika, No. 10, pp. 3–6, October, 1995.     

Predictions of structural,electronic, mechanical,and thermodynamic properties of TMBCs (TM = Ti,Zr, and Hf) ceramics

In the present work, we have investigated the structural, electronic, elastic, and thermodynamic properties of transition-metal boron-carbon compounds (TMBCs) (TM = Ti, Zr, Hf) using the first-principles calculations. The results showed that TMBCs are energetically and thermodynamically stable, and the sequence of phase stability is HfBC > ZrBC > TiBC. B-C bonds can be formed in TMBCs ceramics due to the strong hybridization between B-2p and C-2p states. The elastic anisotropies of TMBCs were illustrated by elastic anisotropy indexes, 3D surface constructions, and 2D projections, and the results indicated that the sequence of elastic anisotropy is ZrBC > TiBC > HfBC. Finally, the calculated minimum thermal conductivities, based on the Clarke's and Cahill's models, of all TMBCs are anisotropic with the sequence of ZrBC > TiBC > HfBC.     

Effect of Li2O on the crystallization behavior of CaO-Al2O3-SiO2-Li2O-Ce2O3 mold slags

The effect of Li₂O on the crystallization properties of CaO-Al₂O₃-SiO₂-Li₂O-Ce₂O₃ slags was investigated. With increasing the Li₂O content, LiAlO₂ and CaCeAlO₄ were the main crystalline phases. LiAlO₂ formed for the charge compensating of Li⁺ ions to [AlO₄^5?]-tetrahedrons, and CaCeAlO₄ formed as a result of the charge balance of Ce³⁺ ions, Ca²⁺ ions, and [AlO₆^9?]-octahedrons. Increasing the content of Li₂O to 10%, the crystallization temperature was the highest, and the incubation time was the shortest. The crystallization ability was strong due to the three factors of strengthening the interaction between ions and ion groups, decreasing the polymerization degree, and increasing the melting temperature. Further increasing the content of Li₂O, the crystallization performance was obviously suppressed, because the melting temperature and the force between the cations and the anion groups decreased.     

The oxidation activity and acid-base properties of SnO2-based binary catalysts: II. The SnO2MoO3 and SnO2P2O5 systems

The vapor-phase oxidation of 1-butene, butadiene, and acetic acid, the isomerization of 1-butene, and the dehydration and dehydrogenation of isopropyl alcohol (IPA) were carried out, in the presence of an excess of air, over two series of catalysts, SnO₂MoO₃, and SnO₂P₂O₅, and the relationship between the catalytic behavior and the acid-base properties of the catalysts was investigated. The acidity and the basicity of the SnO₂MoO₃ catalysts were measured by studying the adsorption of basic and acidic molecules, respectively, in the gas phase, using both the static and pulse methods. The acidities of the SnO₂MoO₃ catalysts are dramatically high at the Mo content of 30–60 atom%, though those of the SnO₂-rich (Mo < 20 atom%) and MoO₃-rich (Mo > 80 atom%) catalysts are fairly low. The basicity is remarkably enhanced by the introduction of a small amount of MoO₃ (Mo < 5 atom%). It can be said that the catalysts are basic in the MoO₃-poor composition. In the case of the SnO₂P₂O₅ catalysts, the acidity and basicity were evaluated from the catalytic activity for the dehydration of IPA to propylene and the (dehydrogenation rate for IPA)/(dehydration rate for IPA) ratio, respectively. The introduction of P₂O₅ increases the acidity and decreases the basicity, to a very small extent, so it cannot cause a remarkable modification in the catalytic behavior; that is, the SnO₂P₂O₅ catalysts are rather basic.     

Influence of Y2O3 on the microstructure and tribological properties of Ti-based wear-resistant laser-clad layers on TC4 alloy

Multi-track Ti-based wear-resistant composite coatings were fabricated on TC4 alloy surfaces using laser-clad TC4 + Ni45 + Co–WC mixed powders with different Y₂O₃ contents (0, 1, and 3 wt%). The microstructure, microhardness, and tribological properties of the coatings were characterised using X-ray diffraction, scanning electron microscopy, energy dispersive spectrometry, electron probe X-ray micro analyser, microhardness tester, and friction and wear testing apparatus. The results showed that the number of cracks on the coating surfaces gradually decreased with the addition of Y₂O₃ and that residual Co–WC powders existed in the coating subsurfaces. The phase composition of the coatings with different Y₂O₃ contents remained unchanged and was mainly composed of reinforcing phases of TiC, TiB₂, Ti₂Ni, and matrix α-Ti. With the addition of Y₂O₃, the coating microstructure was remarkably refined, the direction characteristic of the TiC dendrites obviously weakened, and the nucleation rate significantly increased. When the added Y₂O₃ was 3 wt%, a large amount of TiB₂–TiC-dependent growth composite phases precipitated in the coating. The two-dimensional lattice misfit between (0001)_TiB2 and (111)_TiC was 0.912%, which indicated that TiB₂ and TiC formed a coherent interface. When the amount of Y₂O₃ was increased, the microhardness of the coatings gradually decreased, and the wear volume of the coatings first increased and then decreased. Under the effect of the TiB₂–TiC composite phases, the wear resistance of the 3 wt% Y₂O₃ coating was optimal. The 3 wt% Y₂O₃ coating friction coefficient was the lowest, and the wear mechanism was abrasive wear.     

Nano-sized Sm0.5Sr0.5CoO3−δ as the cathode for solid oxide fuel cells with proton-conducting electrolytes of BaCe0.8Sm0.2O2.9

Nano-sized Sm_0.5Sr_0.5CoO_3−δ (SSC) was fabricated onto the inner face of porous BaCe_0.8Sm_0.2O_2.9 (BCS) backbone by ion impregnation technique to form a composite cathode for solid oxide fuel cells (SOFCs) with BCS, a proton conductor, as electrolyte. The electro-performance of the composite cathodes was investigated as function of fabricating conditions, and the lowest polarization resistance, about 0.21 Ω cm² at 600 °C, was achieved with BCS backbone sintered at 1100 °C, SSC layer fired at 800 °C, and SSC loading of 55 wt.%. Impedance spectra of the composite cathodes consisted of two depressed arcs with peak frequency of 1 kHz and 30 Hz, respectively, which might correspond to the migration of proton and the dissociative adsorption and diffusion of oxygen, respectively. There was an additional arc peaking at 1 Hz in the Nyquist plots of a single cell, which should correspond to the anode reactions. With electrolyte about 70 μm in thickness, the simulated anode, cathode and bulk resistances of cells were 0.021, 0.055 and 0.68 Ω cm² at 700 °C, relatively, and the maximum power density was 307 mW cm⁻² at 700 °C.     

Synthesis and performance of TiB2–B4C composites by high pressure of TiC–B mixture

TiB₂–B₄C composites were in situ synthesized and consolidated by high pressure synthesis method from a mixture of TiC and B powders at the pressure and temperature of 5.0 GPa and 1500℃-1900℃. The phase composition, microstructure, density, hardness, thermal conductivity, and electrical resistivity of TiB₂–B₄C composites were analyzed. As the increase in the synthesis temperature, the products were TiB₂ and B₄C phases and that crystallinity improved. TiB₂–B₄C composites were dense without obvious pores. TiB₂–B₄C composites synthesized at 1800℃ obtained the optimized performance, including the relative density of 98.2%, the Vickers hardness of 31.7 ± 1.2 GPa with the load of 9.8 N, the thermal conductivity of 30.3 ± 0.7 W/(m K), and the electrical resistivity of 3.3 × 10⁻³ Ω cm, respectively. The grain size of the TiB₂–B₄C composites changed with the increase in synthesis temperature, leading to the changes in hardness, thermal conductivity, and electrical resistivity.     

Effects of dietary defatted squid on cholesterol metabolism and hepatic lipogenesis in rats

Male Sprague-Dawley rats were fed a cholesterol-free (Exp. 1) or cholesterol-supplemented (Exp. 2) diet containing 20% casein (control group) or 15% defatted squid and 5% casein (defatted squid group), as protein, for 14 d. Serum and hepatic cholesterol concentrations were lower in rats fed defatted squid than in those fed casein in both cholesterol-free (−20%, P<0.05 and −15%, P<0.05, respectively) and cholesterol-supplemented (−25%, P<0.05 and −15%, P<0.05, respectively) diets. Hepatic triglyceride concentration was lower in the defatted squid than in the control groups in both cholesterol-free (−51%, P<0.05) and cholesterol-supplemented diets (−38%, P<0.01). The activities of cytosolic fatty acid synthase and the NADPH-generating enzymes, malic enzyme and glucose-6-phosphate dehydrogenase, in the liver were lower in the defatted squid than in the control groups in both cholesterol-free (−21%, P<0.01, −33%, P<0.05, and −33%, P<0.01, respectively) and cholesterol-supplemented diets (−34%, P<0.05, −57%, P<0.05, and −67%, P<0.05, respectively). The activity of mitochondrial carnitine palmitoyltransferase in the liver was comparable between the control and defatted squid groups. The activity of Mg²⁺-dependent phosphatidate phosphohydrolase in the liver cytosol was lower in the defatted squid (−9%, P<0.05) than in the control groups only in the cholesterol-free diet. Fecal excretion of total steroids was stimulated by the feeding of defatted squid in both cholesterol-free (+77%, P<0.005) and cholesterol-supplemented diets (+29%, P<0.01). These results suggest that the nonlipid fraction of squid exerts a hypocholesterolemic effect by increasing the excretion of total steroids in feces. The fraction also induces a triglyceride-lowering activity in the liver by decreasing hepatic lipogenesis.     

Electrophoretic deposition of titanium nitride coatings

Electrophoretic deposition of the titanium nitride (TiN) coatings from suspensions prepared by dispersion of TiN particles in triethanolamine (TEA) containing butanol medium was studied. Effects of the TiN particles concentration (C_TiN) on the weight of the deposited coatings, triethanolamine concentration (C_TEA=0.25, 0.5, 0.75, and 1 mL/L) on the Zeta potential of the TiN particles, suspension electrical conductivity and pH, as well as effects of the deposition voltage (V_d=60, 90, and 120 V) and time (t_d =1, 2, and 3 minutes) on the microstructure and thickness of the deposited coatings were investigated. Variations in deposition current density, effective deposition voltage, electrical resistance, and deposited coating weight versus deposition time were recorded. The morphology of the as‐dried coatings was studied using Scanning Electron Microscope (SEM). The results indicated that by increasing the C_TiN the weight of deposits increases linearly up to 40 g/L. For suspensions containing C_TiN=40 g/L, the optimum C_TEA is obtained to be 0.5 mL/L leading to Zeta potential of 43.25 mV. Uniform and crack‐free as‐dried coatings obtained at V_d and t_d of 90 V and 2 minutes, respectively.     

Influence of Gd2O3 on the microstructure and properties of transparent MgAl2O4: Cr3+ ceramic

In this work, MgAl₂O₄: Cr³⁺ transparent ceramics have been synthesized by the hot press sintering techniques, and the effect of the sintering aid Gd₂O₃ and its content on the densification, microstructure, and optical, photoluminescence was studied and discussed. The relative density reached 99.29% with 0.8 wt% Gd₂O₃ as a sintering aid, and the optical transmittance at 686 nm and 1446 nm were approximately 76%. As Gd₂O₃ content continued to increase, the grain size of the ceramics became smaller and uniform, accompanied by some pores with the size of ～1 μm. The ceramics with 4.0 wt% Gd₂O₃ showed a higher transmittance, of 82% at 1446 nm. Additionally, Gd₂O₃ was helpful for Cr³⁺ in the sites of octahedral symmetry, which increased the quantum yield. The quantum yield of MgAl₂O₄: Cr³⁺ with 0.8 wt% Gd₂O₃ was about 0.175, which was 36% higher than that of ceramic without Gd₂O₃. In short, the sintering aid Gd₂O₃ not only contributed to improving the densification, homogenizing the grain size, and heightening the optical transmittance but also enhanced the quantum yield of Cr³⁺.     

Effects of different pH medium on swelling properties of 1,2,4,5-benzenetetracarboxylic-chitosan-filled chitosan bio-composites

Investigating the swelling properties of chitosan (Cs) film was deemed meaningful, as it plays an important role in predicting the life span of the film. Due to the limits in stability properties, the insertion of reinforcement agent is expected to increase the properties of Cs film. To this purpose, 1,2,4,5-benzenetetracarboxylic-chitosan (BTC) filler was inserted into the Cs matrix. The effect on the degree of swelling (Q _t ) and the rate of swelling (Q _r ) of the composite film at varying compositions of BTC filler (0, 2, 4, 6, 8, 10 and 12 wt/v%) was investigated. The Q _r and Q _t both decrease with an increasing BTC content, which may be attributed to the looser packaging structure, and the improvement of the hydrophobic character of the composites film. Thus, the addition of BTC filler, up to 10 wt/v%, makes the Cs film more stable with a prolonged swelling time. Meanwhile, electrostatic interaction and hydrogen bonding between the swelling medium and neutral groups, of the polymeric chains of the composites, contributed to the obtained values of Q _t and Q _r . The FTIR results support the argument for the Q _t and Q _r values of different compositions of BTC filler in the Cs matrix, in the different swelling medium (pH 2–14).     

Characterization of fused Fe-Cu based catalyst for higher alcohols synthesis and DRIFTS investigation of TPSR

Fused Fe-Cu based catalyst for higher alcohols synthesis (HAS) is characterized by XRD, TG-DTA, H₂-TPD and DRIFTS of CO adsorption. The results of XRD reveal that the fused Fe-Cu based catalyst consists of Cu₂O, CuFeO₂ and CuFe₂O₄ species. After reduction, the metallic Fe and Cu are the main species, but minor CuFeO₂ and CuFe₂O₄ species are also present. H₂-TPD shows that in comparison with the pure Fe- or Cu-based sample, the ability of Fe-Cu based catalyst for activation of H₂ is higher and the stronger metal-hydrogen bonds are formed. DRIFTS of CO adsorption indicates that CO is adsorbed on both metal and metal ion sites, where the dissociation of CO to C* and O* species and the formation of CO₂ are observed. In situ DRIFTS investigation of CO + H₂-TPSR over the Fe-Cu based catalyst shows that the dissociative activation of H₂ is more difficult than the activation of CO, and carbonaceous and hydrocarbon fragment species only appears after the dissociative activation of H₂. In addition, HAS over the Fe-Cu based catalyst is very complicated, where various intermediates including = CH₂, − CHO, − OOCH, − OH and − C(= O)-R exist.     

cis-4,7,10,trans-13–22∶4 fatty acid distribution in phospholipids of pectinid species Aequipecten opercularis and Pecten maximus

The distribution of cis-4,7,10,trans-13-docosate-traenoic (c4,7,10,t13–22∶4), a peculiar FA previously isolated in the glycerophospholipids of some pectinid bivalves, was investigated in glycerophospholipid classes and subclasses of separated organs (gills, mantle, gonads, and muscle) of the queen scallop Aequipecten opercularis and the king scallop Pecten maximus. Plasmalogen (Pls) and diacyl + alkyl (Ptd) forms of serine, ethanolamine, and choline glycerophospholipids were isolated by HPLC and their FA compositions analyzed by GC-FID. Pls and Ptd forms of serine glycerophospholipids (PlsSer and PtdSer), and to a lesser extend the Pls form of ethanolamine glycerophospholipids (PlsEtn), were found to be specifically enriched with c4,7,10,t13–22∶4. This specificity was found to decrease in the tested organs in the following order: gills, mantle, gonad, and muscle. In gills, c4,7,10,t13–22∶4 was shown to be the main unsaturated FA of serine glycerophospholipids in both Pls and Ptd forms (23.8 and 19.4 mol%, respectively, for A. opercularis, and 21.0 and 26.2 mol% for P. maximus). These results represent the first comprehensive report on the FA composition of plasmalogen serine subclass isolated from pectinid bivalves. The specific association of the PlsSer with the c4,7,10,t13–22∶4 for the two pectinid species can be paralleled to the specific association of the PlsSer with the non-methylene interrupted (NMI) FA and 20∶1(n−11) observed in mussels, clams, and oysters (Kraffe, E., Soudant, P., and Marty, Y. (2004) Fatty Acids of Serine, Ethanolamine and Choline Plasmalogens in Some Marine Bivalves, Lipids 39, 59–66.) This, led us to hypothesize a similar functional significance for c4,7,10,t13–22∶4, NMI FA, and 20∶1(n−11) associated with PlsSer subclass of bivalves.     

Effect of pasture vs. concentrate diet on CLA isomer distribution in different tissue lipids of beef cattle

This study examined the effects of feeding pasture vs. concentrate on the distribution of CLA isomers in the lipids of longissimus and semitendinosus muscle, liver and heart muscle, and subcutaneous fat in beef bulls. Sixty-four German Holstein and German Simmental bulls were randomly allocated to either an indoor concentrate system or periods of pasture feeding followed by a finishing period on a concentrate containing linseed to enhance their beef content of n−3 PUFA and CLA. The concentrations of CLA isomers in the different tissues were determined by GC and silver ion HPLC. The diet affected the distribution of individual CLA isomers in the lipids of the different tissues. The concentration (mg/100 g fresh tissue) of the most prominent isomer, cis-9,trans-11 18∶2, was increased up to 1.5 times in liver and heart tissue of bulls fed on pasture as compared with concentrate. However, no diet effect was observed for cis-9,trans-11 18∶2 in the lipids of longissimus muscle and subcutaneous fat. In all tissues, the second-most abundant CLA isomer in concentratefed bulls was trans-7,cis-9 18∶2. In contrast, trans-11,cis-13 18∶2 was the second-most abundant CLA isomer in all investigated tissue lipids of pasture-fed bulls. The concentration of the trans-11,cis-13 18∶2 isomer was up to 15 times higher in tissues of pasture-fed bulls as compared with concentrate-fed animals. Furthermone, diet affected the concentrations of the CLA trans,trans 18∶2 isomers. Pasture feeding significantly increased the concentrations of some trans,trans 18∶2 isomers as compared with concentrate, predominantly trans-12,trans-14 18∶2 and trans-11,trans-13 18∶2. Overall, pasture feeding resulted in significantly increased concentrations of the sum of CLA isomers in the lipids of longissimus, muscle, subcutaneous fat, heart and liver muscle of German Holstein and German Simmental bulls, but not in semitendinosus muscle.     

Effect of Mn content on the structure and electrochemical characteristics of La0.7Mg0.3Ni2.975−xCo0.525Mnx (x = 0-0.4) hydrogen storage alloys

The effect of Mn content on the crystal structure and electrochemical characteristics of La_0.7Mg_0.3Ni_2.975−xCo_0.525Mn_x (x = 0, 0.1, 0.2, 0.3, 0.4) alloys has been studied systematically. The results of the Rietveld analyses show that all these alloys mainly consist of two phases: the La(La,Mg)₂Ni₉ phase with the rhombohedral PuNi₃-type structure and the LaNi₅ phase with the hexagonal CaCu₅-type structure. The pressure-composition isotherms shows that the partial substitution of Mn for Ni results in lower desorption plateau pressure and steeper pressure plateau of the alloy electrodes. For a Mn content of x = 0.3, the electrochemical performances, including specific discharge capacity, high rate chargeability (HRC) and high rate dischargeability (HRD), of the alloy are preferable. Moreover, the data of the polarization resistance R_p and the exchange current density I₀ of the alloy electrodes is consistent with the results of HRC and HRD. The hydrogen diffusion coefficient D increases with increasing Mn content, and thereafter increases the low temperature dischargeability (LTD) of the alloy electrodes.     

Determination of number-average and weight-average molecular weights of polymer sample from diffusion and sedimentation velocity measurements in theta solvent

Several methods to determine number-average molecular weight M_n and weight-average molecular weight M_w, of a polymer sample are proposed from diffusion and sedimentation velocity measurements at the θ point. According to these methods, M_n and M_w are determined from the diffusion constant vs. molecular weight relationship, and also from the equations of Svedberg and Flory–Mandelkern, using the 2nd-order and the –2nd-order diffusion constants. These methods have been applied to four samples of polydisperse polystyrene in the θ solvent, cyclohexane at 35°C. It was experimentally ascertained that M_n and M_w of each sample determined by the present methods were in good agreement with the results of column fractionation, light scattering, and calculated values from molecular weight distribution curve within experimental errors. It is concluded that the present methods are useful for determining M_n and M_w, since the reliabilities of M_n and M_w values, which are fundamental quantities of polymer characterization, can be raised by comparing the experimental data observed by conventional methods such as osmotic pressure, light scattering, and the Archibald method with those observed by the present methods.     

CLA isomers in milk fat from cows fed diets with high levels of unsaturated fatty acids

The concentrations of CLA isomers were determined by Ag⁺-HPLC in the milk fat of cows fed a control diet consisting of hay ad libitum and 15 kg of fodder beets or this diet supplemented with oilseeds containing either high levels of oleic acid (rapeseed), linoleic acid (sunflower seed), or α-linolenic acid (linseed). Highly significant (P≤0.001) correlations were found between the daily intakes of oleic acid and the concentration of the CLA isomer trans-7,cis-9 in milk fat; of linoleic acid and the CLA isomers trans-10,trans-12, trans-9,trans-11, trans-8,trans-10, trans-7,trans-9, trans-10,cis-12, cis-9,trans-11, trans-8,cis-10, and trans-7,cis-9; and of α-linolenic acid and the CLA isomers trans-12,trans-14, trans-11,trans-13, cis,trans/trans,cis-12,14, trans-11,cis-13, and cis-11,trans-13. CLA concentrations were also determined in the milk fat of cows grazing in the lowlands (600–650 m), the mountains (900–1210 m), and the highlands (1275–2120 m). The concentrations of many isomers were highest in milk fat from the highlands, but only three CLA isomers (cis-9,trans-11, trans-11,cis-13, and trans-8,cis-10) showed a nearly linear increase with elevation. Therefore, these three CLA isomers, and particularly the CLA isomer trans-11,cis-13, the second-most important CLA in milk fat from cows grazing at the three altitudes, could be useful indicators of milk products of Alpine origin.     

Homo- and copolymerizations of ethylene and α-olefins in <Emphasis Type="Italic">n</Emphasis>-hexane catalyzed by Ni(ii)-α-diimine catalyst

Ni(II)-α-diimine catalyst [(2,6-i-Pr)₂C₆H₃-DAB(An)]NiBr₂ plus methylaluminoxane was successfully used in the homopolymerization of ethylene, 1-hexene, and 1-octene and the copolymerization of ethylene with 1-hexene and 1-octene in n-hexane. The polymerization of 1-octene was conducted in a controlled manner with a narrow molecular weight distribution (M _w/M _n = 1.2–1.5) and with the weight-average molecular weight increasing linearly with the monomer conversion. The molecular weights, T _g, T _m, branching degree, and density of the obtained (co)polymers were greatly controlled by ethylene pressure and polymerization temperature. Compared with that of ethylene homopolymer, the branching degree of the copolymers prepared by the copolymerization of ethylene with 1-hexene or 1-octene increased, whereas the molecular weight, density, T _m, and catalyst activity decreased. However, compared with those of the homopolymer of 1-hexene or 1-octene, the copolymer density, T _m, and catalyst activity increased, whereas the branching degree declined.     

Pore and microstructure change induced by SiC whiskers and particles in porous TiB2–TiC–Ti3SiC2 composites

TiB₂–TiC–Ti₃SiC₂ porous composites were prepared through a plasma heating reaction using powder mixtures of Ti, B₄C SiC whiskers (SiC_w) and SiC particles (SiC_p). The effects of the SiC_w and SiC_p content on pore structures, phase constituents, microstructure, and crystal morphology of TiC were studied. The results show that TiC, TiB, Ti₃B₄ phases are formed within the 5Ti+B₄C system. With the addition of SiC_w and SiC_p, the TiB and Ti₃B₄ phases are reduced, sometimes even disappeared. Interestingly, the content of TiB₂ and TiC increased, resulting in Ti₃SiC₂ and TiSi₂ being formed. The porosity of composites increases notably with the addition of SiC_w. However, with the increase of SiC_p, the porosity of the composites first decreases, followed by an increase. After adding the specified amount of SiC_w/SiC_p, the compressive strength of composites are improved significantly. Additionally, the pore size of the composites are decreased significantly with the addition of SiC_w/SiC_p. During the plasma heating process, some Si atoms will diffuse into the TiC lattice, which in turn made the cubic TiC grains into hexagonal lamellar TiC or Ti₃SiC₂ grains.