Isolation,purification, and antioxidant activities of polysaccharides from Ziziphus Jujuba cv. Muzao

In the present study, crude polysaccharides from Ziziphus Jujuba cv. Muzao were isolated and purified using DEAE cellulose-52 and Sephadex G-100 size-exclusion chromatography; four fractions were collected, namely GZMP-1, GZMP-2, GZMP-3, and GZMP-4. The molecular weights of these four fractions were measured to be 111.2, 95.1, 84.2, and 571.4 kDa, respectively, using high-performance gel permeation chromatography. Gas chromatography analysis of the monosaccharide composition confirmed that GZMP-1 was composed of rhamnose, arabinose, glucose, and galactose. Rhamnose, arabinose, and galactose were the main components present in GZMP-2 and GZMP-3, whereas GZMP-4 was composed of only rhamnose and arabinose. Scanning electron microscopy showed relatively smooth surfaces for GZMP-1 and GZMP-4, whereas GZMP-2 and GZMP-3 had more folds on their surfaces. Fourier transform infrared spectroscopy analyses indicated that GZMP-1 and ZMP mainly had α-type glycosidic linkages. The in vitro antioxidant activities of the polysaccharides revealed that jujube polysaccharides exhibit remarkable antioxidant activity, and can scavenge DPPH radical and OH radical in a concentration-dependent manner. The results of this work suggest that polysaccharides from Z. Jujuba cv. Muzao have potential to be used as functional food and in the development of natural antioxidant drug carriers.     

Beneficial role of carbon black on the properties of TiC ceramics

This investigation aimed to study the influence of carbon black on the qualifications of TiC-based materials. For this objective, two samples, namely monolithic TiC and TiC-5 wt% carbon black were sintered by spark plasma sintering (SPS) method at 1900 °C. X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) were used to characterize the as-sintered samples. Introducing carbon black enhanced the relative density of TiC significantly, reaching a near fully dense substance. Phase analysis and microstructural studies manifested the formation of non-stoichiometric TiC_x in both ceramics. Although the introduction of carbonaceous additive considerably increased the thermal conductivity and flexural strength of TiC, standing at 25.1 W/mK and 658 MPa, respectively, its influence on the Vickers hardness was trivial (both ~ 3200 HV_0.1 kg). Finally, the composite specimen presented a lower coefficient of friction (~ 0.31) on average compared to the undoped TiC (~ 0.34).     

Experimental and theoretical approaches for electrical,magnetic, micromechanical,and structural characterization of BSCCO ceramic superconductors

This study investigates how the preparation and re-pelletization of BSCCO ceramic superconductors affects their structural, magnetic, electrical, and mechanical properties. Samples were prepared using conventional methods including the dry solid state (SS) reaction and wet ammonium nitrate (AN) precipitation, with three variations prepared for each technique. The fabricated samples were then characterized with X-ray powder diffraction (XRD) and scanning electron microscopy. The density, resistance vs. temperature characteristics, AC susceptibility vs. temperature characteristics, and magnetic hysteresis properties were measured. In addition, Vicker's microhardness was measured and revealed that all six samples exhibit the reverse indentation size effect (RISE). Microhardness modeling was also conducted. Calculations with Meyer's law, the Hays and Kendall model, and the proportional sample resistance model indicate that the samples are far from the plateau region, whereas the indentation-induced cracking model was consistent with the experimental results. The elastic modulus, Young's modulus, yield strength, and brittleness index were also calculated for each sample.     

The effect of synthesis conditions on the physicochemical properties of magnesium aluminate materials

Magnesium aluminate-based materials were prepared by applying different methods: (i) mechanochemical milling of the initial mixture of magnesium and aluminium nitrate powders (in appropriate stoichiometric amounts) followed by heat treatment at temperatures of 650 °C and 850 °C and (ii) melting of the mixture of nitrate precursors at 240 °C followed by thermal treatment at 650 °C, 750 °C and 850 °C. The effect of synthesis method on the structure and morphology of the obtained solids was studied by using various techniques such as: nitrogen adsorption-desorption isotherms, powder XRD, IR spectroscopy and SEM. It was shown that the mechanochemical milling performed before calcination procedure leads to obtaining of nanocrystalline magnesium aluminate spinel phase at lower temperature of 650 °C in comparison with the method using thermal treatment only (at 750 °C). The obtained nanomaterials exhibit mesoporous structure.     

Complementary characterization methods for Lithium-ion Polymer secondary battery modeling

This paper deals with the electrical modeling of Lithium-ion Polymer battery, from complementary characterization tests. The first aim of this work is to understand the electrical behavior of this battery through experimentations in the same environmental conditions as the final application’s ones. The second goal of this work is to identify battery models with different precision levels and to implement them in specific models of the considered aircraft electrical network. In this paper, two equivalent electrical circuit models are presented: a quasi-static model, which is functional and sufficient for the electrical energy management in the aircraft; a dynamic model, which is behavioral and necessary for the analysis of the embedded network quality. The identification of their parameters is carried out with adapted characterization tests, such as chronopotentiometry at constant current and Electrochemical Impedance Spectroscopy at different temperatures. The complementarity of these tests is particularly underlined in this paper because it is useful for the parameter identification. The results from model simulation and from experimentation are compared through a mission profile and are analyzed. Eventually, this paper presents complete experimental data for a commercial 4.8 Ah Lithium-ion Polymer battery including the temperature influence.     

Wild melon: a novel non-edible feedstock for bioenergy

In the present research work, a non-edible oil source Cucumis melo var. agrestis(wild melon) was systematically identified and studied for biodiesel production and its characterization. The extracted oil was 29.1% of total dry seed weight. The free fatty acid value of the oil was found to be 0.64%, and the single-step alkaline transesterification method was used for conversion of fatty acids into their respective methyl esters. The maximum conversion efficiency of fatty acids was obtained at 0.4 wt% Na OH(used as catalyst), 30%(methanol to oil, v/v) methanol amount, 60 ℃ reaction temperature,600-rpm agitation rate and 60-min reaction time. Under these optimal conditions, the conversion efficiency of fatty acid was 92%. However, in the case of KOH as catalyst, the highest conversion(85%) of fatty acids was obtained at 40%methanol to oil ratio, 1.28 wt% KOH, 60 ℃ reaction temperature, 600-rpm agitation rate and 45 min of reaction time.Qualitatively, biodiesel was characterized through Fourier transform infrared spectroscopy(FTIR) and gas chromatography and mass spectroscopy(GC–MS). FTIR results demonstrated a strong peak at 1742 cm~(-1), showing carbonyl groups(C=O)of methyl esters. However, GC–MS results showed the presence of twelve methyl esters comprised of lauric acid, myristic acid, palmitic acid, non-decanoic acid, hexadecanoic acid, octadecadienoic acid and octadecynoic acid. The fuel properties were found to fall within the range recommended by the international biodiesel standard, i.e., American Society of Testing Materials(ASTM): flash point of 91 ℃, density of 0.873 kg/L, viscosity of 5.35 c St, pour point of-13 ℃, cloud point of-10 ℃, total acid number of 0.242 mg KOH/g and sulfur content of 0.0043 wt%. The present work concluded the potential of wild melon seed oil as excellent non-edible source of bioenergy.     

低温溶液缩聚法制备聚间苯二甲酰对苯二胺

采用低温溶液缩聚法制备了聚间苯二甲酰对苯二胺(PPIA),讨论了单体浓度、单体物质的量配比、反应温度等因素对聚合反应的影响,并用红外光谱(IR)、热重分析(TG)、X射线衍射(XRD)、扫描电镜(SEM)对实验产物进行了测定。红外检测出的特征峰符合PPIA的结构特征,热重测得热分解速率最大温度在520℃左右,X射线衍射表明聚合物有明显结晶现象,并且扫描电镜显示下的聚合物结构聚集状态良好。     

Microporous polyvinylidene fluoride hollow fiber membrane contactors for CO2 stripping: Effect of PEG-400 in spinning dope

In order to develop the structure of microporous PVDF membranes, PEG-400 was introduced into the polymer dope as a non-solvent additive. The hollow fiber membranes were prepared via a wet phase-inversion process and then used in the membrane contactor modules for CO₂ stripping from water. By addition of different amounts of PEG-400, cloud points of the polymer dope were obtained to examine phase-inversion behavior. From FESEM analysis, the membrane structure changed from a finger-like to an approximately sponge-like morphology with the addition of 4 wt.% of PEG-400. The prepared membranes presented smaller mean pore size (0.13 μm) and significantly higher wetting pressure (550 kPa) compared to the plain membrane. From CO₂ stripping test, at water velocity of 0.4 m/s, the PVDF membranes prepared by 4% PEG-400 demonstrated an approximate CO₂ stripping flux of 4.5 × 10⁻⁵ (mol/m² s) which is 125% higher than the flux of the plain membrane. It could be concluded that structurally developed hydrophobic PVDF hollow fiber membranes can be prepared by a controlled phase-inversion process to enhance the performance of gas–liquid membrane contactor.     

Synthesis and Surface Properties of Novel Gemini Imidazolium Surfactants

Five new Gemini imidazolium surfactants were synthesized from imidazole and 1-bromoalkane (C₈, C₁₀, C₁₂, C₁₄, C₁₆) to get 1-alkylimidazole, which was further reacted with 1,3-dichloropropan-2-ol to form the surfactant molecule, 1,1′-(propane-1,3-diyl-2-ol) bis(3-alkyl-1H-imidazol-3-ium) chloride. The structures of the five new surfactants and intermediates were characterized by ¹H-NMR, ¹³C-NMR and IR spectra. Thermal properties of the five new surfactants were studied with thermogravimetric analysis and differential scanning calorimetry, the five new surfactants showed a transition from a crystalline phase to a thermotropic liquid–crystalline phase at around ca. 100 °C, which transformed to an isotropic liquid phase at around ca. 165 °C. The five new surfactants critical micelle concentrations (CMC) in the aqueous solutions were determined by surface tension and electrical conductivity methods. The surface tension measurements provided a series of parameters, including critical micelle concentration (CMC), surface tension at the CMC (γ _CMC), adsorption efficiency  (pC ₂₀), and effectiveness of surface tension reduction (π_CMC). In addition, with application of the Gibbs adsorption isotherm, maximum surface excess concentration (Γ_max) and minimum surface area/molecule (A_min) at the air–water interface were obtained. The parameters β (degree of counterion binding to micelles), ΔG _ads ^θ (Gibbs free energy of adsorption), and ΔG _mic ^θ (Gibbs free energy change of micellization) were also derived. The results indicated that the five new Gemini surfactants exhibited very low CMC and a good efficiency in lowering the surface tension of water. The foamability and foam stability of the five new surfactants were also examined at different CMC.     

Soluble microbial products formation in anaerobic chemostats in the presence of toxic compounds

Anaerobic chemostats fed on glucose (approximately 10 g chemical oxygen demand (COD)/L) were used to investigate the effects of toxicity on soluble microbial product (SMP) formation. Addition of the toxic compounds chloroform and chromium increased the net accumulation of SMP, despite reducing the percentage of SMP in the effluent due to the overwhelming production of volatile fatty acids (VFAs). In the reactor spiked with chloroform the normalized accumulation of SMP (SMP/So) increased from 2% to 8%, whereas in the reactor spiked with Cr (VI) the SMP/So ratio reached as high as 20% after the spike, and in both cases SMP net accumulation was proportional to the concentration of toxicant. After the chloroform and chromium spikes biomass seemed to produce more extra cellular polymeric substances (EPS) suggesting that this might have helped them to cope with the stress. Chromatography results indicate that some of the high MW compounds present in the SMP might have been due to EPS release into the bulk solution, and that other compounds, probably released as a result of cell lysis, were also present. Hydrolysis of EPS did not seem to contribute to SMP accumulation in the presence of toxic compounds, and DNA analysis suggested that cell lysis products was an important contribution to SMP accumulation, in the presence of chromium.