Evaluating the electrochemical properties of PEO‐based nanofibrous electrolytes incorporated with TiO2 nanofiller applicable in lithium‐ion batteries

In the present work, nanofibrous composite polymer electrolytes consist of polyethylene oxide (PEO), ethylene carbonate (EC), propylene carbonate (PC), lithium perchlorate (LiClO₄), and titanium dioxide (TiO₂) were designed using response surface method (RSM) and synthesized via an electrospinning process. Morphological properties of the as‐prepared electrolytes were studied using SEM. FTIR spectroscopy was conducted to investigate the interaction between the components of the composites. The highest room temperature ionic conductivity of 0.085 mS.cm^?1 was obtained with incorporation of 0.175 wt. % TiO₂ filler into the plasticized nanofibrous electrolyte by EC. Moreover, the optimum structure was compared with a film polymeric electrolyte prepared using a film casting method. Despite more amorphous structure of the film electrolyte, the nanofibrous electrolyte showed superior ion conductivity possibly due to the highly porous structure of the nanofibrous membranes. Furthermore, the mechanical properties illustrated slight deterioration with incorporation of the TiO₂ nanoparticles into the electrospun electrolytes. This investigation indicated the great potential of the electrospun structures as all‐solid‐state polymeric electrolytes applicable in lithium ion batteries.     

High‐Performance Oxygen Sensors Based on EuIII Complex/Polystyrene Composite Nanofibrous Membranes Prepared by Electrospinning

An optical oxygen sensor based on an Eu^III complex/polystyrene (PS) composite nanofibrous membrane is prepared by electrospinning. The emission intensity of [Eu(TTA)₃(phencarz)] (TTA=2‐thenoyltrifluoroacetonate, phencarz=2‐(N‐ethylcarbazolyl‐4)imidazo[4,5‐f]1,10‐phenanthroline) decreases with increasing oxygen concentration, and thus the [Eu(TTA)₃ (phencarz)]/PS composite nanofibrous membranes can be used as an optical oxygen‐sensing material based on emission quenching caused by oxygen. Elemental analysis, UV/Vis absorption spectra, scanning electron microscopy (SEM), fluorescence microscopy, luminescence‐intensity quenching Stern–Volmer plots, and excited‐state decay analysis are used to characterize the obtained oxygen‐sensing materials. A high sensitivity (I_N2/I_O2) of 3.38 and short response and recovery times (t_↓=5.0, t_↑=8.0 s) are obtained. These results are the best values reported for oxygen sensors based on Eu^III complexes. The high surface area‐to‐volume ratio and porous structure of the electrospun nanofibrous membranes are taken to be responsible for the outstanding performance.     

A nanofibrous composite membrane of PLGA-chitosan/PVA prepared by electrospinning

Tissue engineering scaffolds produced by electrospinning feature a structural similarity to the natural extracellular matrix. In this study, poly(lactide-co-glycolide) (PLGA) and chitosan/poly(vinyl alcohol) (PVA) were simultaneously electrospun from two different syringes and mixed on the rotating drum to prepare the nanofibrous composite membrane. The composite membrane was crosslinked by glutaraldehyde vapor to maintain its mechanical properties and fiber morphology in wet stage. Morphology, shrinkage, absorption in phosphate buffered solution (PBS) and mechanical properties of the electrospun membranes were characterized. Fibroblast viability on electrospun membranes was discussed by MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide] assay and cell morphology after 7 days of culture. Results indicated that the PBS absorption of the composite membranes, no matter crosslinked or not, was higher than the electrospun PLGA membrane due to the introduction of hydrophilic components, chitosan and PVA. After crosslinking, the composite membrane had a little shrinkage after incubating in PBS. The crosslinked composite membrane also showed moderate tensile properties. Cell culture suggested that electrospun PLGA-chitosan/PVA membrane tended to promote fibroblast attachment and proliferation. It was assumed that the nanofibrous composite membrane of electrospun PLGA-chitosan/PVA could be potentially used for skin reconstruction.     

Controlled assembly of superparamagnetic iron oxide nanoparticles on electrospun PU nanofibrous membrane: A novel heat-generating substrate for magnetic hyperthermia application

A facile method of fabricating novel heat-generating membranes composed of electrospun polyurethane (PU) nanofibers decorated with superparamagnetic iron oxide nanoparticles (NPs) is reported. Electrospinning was used to produce polymeric nanofibrous matrix, whereas polyol immersion technique allowed in situ assembly of well-dispersed Fe₃O₄ NPs on the nanofibrous membranes without any surfactant, and without sensitizing and stabilizing reagent. The assembly phenomena can be explained by the hydrogen-bonding interactions between the amide groups in the PU matrix and the hydroxyl groups capped on the surface of the Fe₃O₄ NPs. The prepared nanocomposite fibers showed acceptable magnetization value of 33.12 emu/g, after measuring the magnetic hysteresis loops using SQUID. Moreover, the inductive heating property of electrospun magnetic nanofibrous membranes under an alternating current (AC) magnetic field was investigated. We observed a progressive increase in the heating rate with the increase in the amount of magnetic Fe₃O₄ NPs in/on the membranes. The present electrospun magnetic nanofibrous membrane may be a potential candidate as a novel heat-generating substrate for localized hyperthermia cancer therapy.     

聚乙烯亚胺修饰的氧化硅纳米管基吸附剂的制备及其CO_2吸附应用

以P123为模板,1,2-二(三甲氧基硅基)乙烷(BTME)为硅源合成了介孔氧化硅纳米管(E-SNTs).将ESNTs经过聚乙烯亚胺(PEI)修饰后制得吸附剂用于捕捉CO2.对吸附剂进行了透射电镜(TEM)、物理吸附、傅里叶变换红外(FTIR)光谱、热重分析(TGA)等表征.E-SNTs-PEI吸附剂的最佳CO2吸附温度为75°C.吸附剂的CO2吸附量随着PEI负载量的增加呈现先增大后减小的趋势,其中50%为最佳负载量,此时吸附剂的吸附量最大为3.32 mmol·g-1.相比较SBA-15基吸附剂,E-SNTs基吸附剂具有更优异的吸附性能.在有水汽的存在下,吸附剂E-SNTs-50的CO2吸附量达到3.75 mmol·g-1.经过四次循环吸脱附实验测试E-SNTs-PEI吸附剂的稳定性能,结果表明其CO2吸附量基本不变,该吸附剂表现出较好的稳定性和可再生能力.     

A Density Functional Theory Study on the Effect of Zero‐Point Energy Corrections on the Methanation Profile on Fe(100)

The thermodynamics and kinetics of the surface hydrogenation of adsorbed atomic carbon to methane, following the reaction sequence C+4 H?CH+3 H?CH₂+2 H?CH₃+H?CH₄, are studied on Fe(100) by means of density functional theory. An assessment is made on whether the adsorption energies and overall energy profile are affected when zero‐point energy (ZPE) corrections are included. The C, CH and CH₂ species are most stable at the fourfold hollow site, while CH₃ prefers the twofold bridge site. Atomic hydrogen is adsorbed at both the twofold bridge and fourfold hollow sites. Methane is physisorbed on the surface and shows neither orientation nor site preference. It is easily desorbed to the gas phase once formed. The incorporation of ZPE corrections has a very slight, if any, effect on the adsorption energies and does not alter the trends with regards to the most stable adsorption sites. The successive addition of hydrogen to atomic carbon is endothermic up to the addition of the third hydrogen atom resulting in the methyl species, but exothermic in the final hydrogenation step, which leads to methane. The overall methanation reaction is endothermic when starting from atomic carbon and hydrogen on the surface. Zero‐point energy corrections are rarely provided in the literature. Since they are derived from C? H bonds with characteristic vibrations on the order of 2500–3000 cm^?1, the equivalent ZPE of 1/2 hν is on the order of 0.2–0.3 eV and its effect on adsorption energy can in principle be significant. Particularly in reactions between CH_x and H, the ZPE correction is expected to be significant, as additional C? H bonds are formed. In this instance, the methanation reaction energy of +0.77 eV increased to +1.45 eV with the inclusion of ZPE corrections, that is, less favourable. Therefore, it is crucial to include ZPE corrections when reporting reactions involving hydrogen‐containing species.     

Measurement of size‐dependent glass transition temperature in electrospun polymer fibers using AFM nanomechanical testing

The glass transition temperature (T_g) of individual electrospun polymer polyvinyl alcohol fibers of varying diameter was measured using atomic force microscopy (AFM) based nanomechanical thermal analysis. Indentation and bending of individual electrospun fibers using AFM allowed the calculation of the elastic modulus of the polyvinyl alcohol (PVA) fibers across a range of different temperatures. The elastic modulus of electrospun PVA fibers was observed to decrease significantly when passing through T_g, which allowed accurate determination of T_g. The T_g of electrospun PVA fibers was shown to decrease for smaller fiber diameters especially for fiber diameters below 250 nm. This size‐dependent glass transition behavior of electrospun PVA fibers is indicated as being due to polymer chain confinement. © 2011 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2011     

Activation of Methane Promoted by Adsorption of CO on Mo2C2− Cluster Anions

Atomic clusters are being actively studied for activation of methane, the most stable alkane molecule. While many cluster cations are very reactive with methane, the cluster anions are usually not very reactive, particularly for noble metal free anions. This study reports that the reactivity of molybdenum carbide cluster anions with methane can be much enhanced by adsorption of CO. The Mo₂C₂^? is inert with CH₄ while the CO addition product Mo₂C₃O^? brings about dehydrogenation of CH₄ under thermal collision conditions. The cluster structures and reactions are characterized by mass spectrometry, photoelectron spectroscopy, and quantum chemistry calculations, which demonstrate that the Mo₂C₃O^? isomer with dissociated CO is reactive but the one with non‐dissociated CO is unreactive. The enhancement of cluster reactivity promoted by CO adsorption in this study is compared with those of reported systems of a few carbonyl complexes.     

Epidermal cellular response to poly(vinyl alcohol) nanofibers containing silver nanoparticles

A heat-treated PVA nanofibrous matrix containing silver (Ag) was prepared by electrospinning an aqueous 10 wt% PVA solution and followed by heat treatment at 150 °C for 10 min. The average diameter of the as-spun and heat-treated PVA nanofibers was 330 nm. The heat-treated PVA nanofibrous matrix containing Ag was irradiated with UV light to transform the Ag ions in the nanofibrous matrix into Ag nanoparticles. The in vitro cytotoxicity of the Ag ions and/or nanoparticles on normal human epidermal keratinocytes (NHEK) and fibroblasts (NHEF) cultures was examined. The PVA nanofibrous matrix containing Ag showed slightly higher level of attachment and spreading in the early stage culture (1 h) than the PVA nanofibers without Ag (control). However, compared with the PVA nanofibers without Ag, the heat-treated and UV-irradiated PVA nanofibers, containing mainly Ag ions and nanoparticles, respectively, showed reduced cell attachment and spreading. This shows that both Ag ions and Ag nanoparticles are cytotoxic to NHEK and NHEF. There was no significant difference in cytotoxicity to NHEK and NHEF between Ag ions and Ag nanoparticles. NHEF appeared to be more sensitive to Ag ions or particles than NHEK. In addition, the residual nitrate ions (NO₃⁻) in the PVA nanofibers had an adverse effect on the culture of both cells.     

Stabilization of electrospun poly(vinyl alcohol) nanofibrous mats in aqueous solutions

<正>The stability ofpoly(vinyl alcohol)(PVA) nanofibrous mats in water media was improved by post-electrospinning treatments.Bifunctional glutaraldehyde(GA) in methanol was used as a crosslinking agent to stabilize PVA nanofiber,but fiber twinning was observed frequently,and the highly porous structure of PVA nanofibrous mats was destroyed when the crosslinked fiber was soaked in water.To overcome this shortcoming,chitosan(CS) was introduced into the PVA spinning solution to prepare PVA/CS composite nanofibers.Their treatment in GA/methanol solution could retain the fiber morphology of PVA/CS nanofibers and porous structure of PVA/CS nanofibrous mats even if they were soaked in aqueous solutions for 1 month.Scanning electron microscopy(SEM),X-ray diffraction(XRD),thermal gravimetric analysis(TGA) and differential scanning calorimetry(DSC) were applied to characterize the physicochemical structure and thermal properties of PVA nanofibers.It was found that the water resistance of PVA nanofibrous mats was enhanced because of the improvement of the degree of crosslinking and crystallinity in the electrospun PVA fibers after soaking in GA/methanol solution.     

Kinetic study of the reaction of OH with a series of acetals at 298 ± 4 K

Rate coefficients have been measured at 298 ± 4 K and 1000 mbar total pressure for the reactions of OH with a series of symmetrical acetals (R O CH₂ O R, R = C₁ to C₄) using a relative kinetic technique. The investigations have been performed in a laboratory photoreactor and also in the large outdoor EUPHORE simulation chamber facility in Valencia, Spain. The following rate coefficients (in units of 10⁻¹¹ cm³ molecule⁻¹ s⁻¹) have been obtained: dimethoxy methane (R = CH₃), 0.49 ± 0.02; diethoxy methane (R = CH₃CH₂), 1.84 ± 0.18; di‐n‐propoxy methane (R = CH₃CH₂CH₂), 2.63 ± 0.49; di‐iso‐propoxy methane (R = (CH₃)₂CH), 3.93 ± 0.48; di‐n‐butoxy methane (R = CH₃CH₂CH₂CH₂), 3.47 ± 0.42; di‐iso‐butoxy methane (R = (CH₃)₂CHCH₂), 3.68 ± 0.57; di‐sec‐butoxy methane (R = CH₃CH₂C(CH₃)H), 4.68 ± 0.05. © 1999 John Wiley & Sons, Inc. Int J Chem Kinet 31: 797–803, 1999     

Comparative study of CTAB adsorption on bituminous coal and clay mineral

Adsorption of cetyltrimethylammonium bromide (CTAB) onto bituminous coal (BC) and a clay mineral, montmorillonite (MMT), was studied. Simultaneous measurements of the CTAB adsorption and zeta potential determination of the adsorption suspensions were carried out. The adsorption isotherms were found to be of the typical Langmuir type; values of the CTAB adsorption capacities were calculated (a _m = 0.65 mmol g⁻¹ for coal and a _m = 3.24 mmol g⁻¹ for MMT). The shape of the adsorption isotherms was correlated with zeta potential values at the adsorption equilibrium. The adsorption properties of both sorbents were studied by voltammetry on carbon paste electrodes (CPE) modified with coal-CTAB and MMT-CTAB system, respectively. Open circuit sorption with differential pulse voltammetry was performed in order to compare the sorption properties of the systems with the unmodified sorbents. The Cu²⁺ adsorption on BC and MMT decreased to approximately 50 % and 40 %, respectively. The surface adsorption mechanism of CTAB on coal based on hydrophilic interactions was proposed. In the case of montmorillonite, the CTAB intercalation is expected via ion exchange into the inter-layer space forming a double- or triple-layer arrangement.     

Investigation of hydrogen and methane adsorption/separation on silicon nanotubes: a hierarchical multiscale method from quantum mechanics to molecular simulation

A combination of ab initio quantum mechanical (QM) calculations and canonical Monte Carlo (CMC) simulations are employed to investigate possible usage of single-walled silicon nanotubes (SWSiNTs) as a novel media for hydrogen and methane adsorption as well as their separation from each other. By fitting the force field, a Morse potential model is selected as an efficient potential to describe the binding energies between both hydrogen-SiNTs and methane-SiNTs obtained from ab initio calculations. Then CMC simulations are performed to evaluate the adsorption and separation behaviors of H₂ and CH₄ on the three different sizes of SiNTs including (5, 5), (7, 7), and (9, 9) SiNTs at ambient temperatures and pressures from 1 up to 10 MPa. As a comparison, the adsorption and separation of H₂ and CH₄ on the (8, 8) CNTs which are isodiameter with (5, 5) SiNTs are also simulated. Results are indicative of remarkable enhancement of H₂ and CH₄ adsorption capacity on the SiNTs compared to the CNTs, which arise from stronger van der Waals (VDW) attractions. In the case of methane adsorption on SiNTs, the stored volumetric energy exceeds the goal of the US Freedom CAR Partnership by 2010, which can not be achieved by methane compression at such low pressures. Moreover, simulation results indicate that SiNTs preferentially adsorb methane relative to hydrogen in their equimolar mixture, which results in efficient separation of these gases from each other at 293 K.     

Novel Ni/CeO2-Al2O3 composite catalysts synthesized by one-step citric acid complex and their performance in catalytic partial oxidation of methane

A series of novel Ni/CeO2-Al2O3composite catalysts were synthesized by one-step citric acid complex method. The as-synthesized catalysts were characterized by N2physical adsorption/desorption, X-ray diffraction(XRD), Fourier transform infrared(FT-IR) spectroscopy, hydrogen temperature-programmed reduction(H2-TPR), X-ray photoelectron spectroscopy(XPS) and thermogravimetry analysis(TGA). The effects of nickel content, calcination and reaction temperatures, gas hourly space velocity(GHSV) and inert gas dilution of N2on their performance of catalytic partial oxidation of methane(CPOM) were investigated. Catalytic activity test results show that the highest methane conversion(85%), the best selectivities to carbon monoxide(87%) and to hydrogen(95%), the excellent stability and perfect H2/CO ratio(2.0) can be obtained over Ni/CeO2-Al2O3with 8 wt% Ni content calcined at 700 ℃ under the reaction condition of 750 ℃, CH4/O2ratio of 2 : 1 and gas hourly space velocity of 12000 mL h-1 g-1. Characterization results show that the good catalytic performance of this composite catalyst can be contributed to its large specific surface area(～108 m2 g-1), small crystallite size, easy reducibility and low coking rate.     

In Situ Investigation of Methane Dry Reforming on Metal/Ceria(111) Surfaces: Metal–Support Interactions and C−H Bond Activation at Low Temperature

Studies with a series of metal/ceria(111) (metal=Co, Ni, Cu; ceria=CeO₂) surfaces indicate that metal–oxide interactions can play a very important role for the activation of methane and its reforming with CO₂ at relatively low temperatures (600–700 K). Among the systems examined, Co/CeO₂(111) exhibits the best performance and Cu/CeO₂(111) has negligible activity. Experiments using ambient pressure X‐ray photoelectron spectroscopy indicate that methane dissociates on Co/CeO₂(111) at temperatures as low as 300 K—generating CH_x and CO_x species on the catalyst surface. The results of density functional calculations show a reduction in the methane activation barrier from 1.07 eV on Co(0001) to 0.87 eV on Co²⁺/CeO₂(111), and to only 0.05 eV on Co⁰/CeO_2−x (111). At 700 K, under methane dry reforming conditions, CO₂ dissociates on the oxide surface and a catalytic cycle is established without coke deposition. A significant part of the CH_x formed on the Co⁰/CeO_2−x (111) catalyst recombines to yield ethane or ethylene.     

Improved cellular response on multiwalled carbon nanotube-incorporated electrospun polyvinyl alcohol/chitosan nanofibrous scaffolds

We report the fabrication of multiwalled carbon nanotube (MWCNT)-incorporated electrospun polyvinyl alcohol (PVA)/chitosan (CS) nanofibers with improved cellular response for potential tissue engineering applications. In this study, smooth and uniform PVA/CS and PVA/CS/MWCNTs nanofibers with water stability were formed by electrospinning, followed by crosslinking with glutaraldehyde vapor. The morphology, structure, and mechanical properties of the formed electrospun fibrous mats were characterized using scanning electron microscopy, Fourier transform infrared spectroscopy, and mechanical testing, respectively. We showed that the incorporation of MWCNTs did not appreciably affect the morphology of the PVA/CS nanofibers; importantly the protein adsorption ability of the nanofibers was significantly improved. In vitro cell culture of mouse fibroblasts (L929) seeded onto the electrospun scaffolds showed that the incorporation of MWCNTs into the PVA/CS nanofibers significantly promoted cell proliferation. Results from this study hence suggest that MWCNT-incorporated PVA/CS nanofibrous scaffolds with small diameters (around 160 nm) and high porosity can mimic the natural extracellular matrix well, and potentially provide many possibilities for applications in the fields of tissue engineering and regenerative medicine.     

Forward ion-exchange kinetics of heavy metal ions on the surface of carboxymethyl cellulose Sn(IV) phosphate composite nano-rod-like cation exchanger

The Nernst?CPlanck equations with some additional assumptions was used in this study to investigate the forward kinetics and ion-exchange mechanism of heavy metal ions viz. Ni²⁺?CH⁺, Cu²⁺?CH⁺, Mn²⁺?CH⁺ and Zn²⁺?CH⁺ on the surface of carboxymethyl cellulose Sn(IV) phosphate composite nano-rod-like cation-exchanger. It was observed that heavy metals' exchange processes were imparted by the particle diffusion-controlled phenomenon. Some physical parameters i.e., fractional attainment of equilibrium U(??), self-diffusion coefficients (D _o), energy of activation (E _a), and entropy of activation (??S*) were estimated. These investigations revealed that the equilibrium is attained faster at higher temperature probably because of availability of thermally enlarged matrix of carboxymethyl cellulose Sn(IV) phosphate composite nano-rod-like cation-exchange material. The physical parameters observed for this composite cation exchanger were also compared with other composite ion exchangers. The results showed that the ion-exchange phenomenon is more feasible on the surface of this composite cation exchanger as compared with the other ion exchangers which indicated the usefulness of this composite ion exchanger in various applications.     

Hydrocarbon specificity in the selective catalytic reduction of NOx over Cu-ZSM-5 and Co-ZSM-5 catalysts

Transformation of surface nitrates under CH₄ (CH₄+O₂) was found to ensure steady-state activity of Co-ZSM-5 in the selective catalytic reduction of nitrogen oxides by methane (CH₄-SCR). For Cu-ZSM-5, such species are mainly converted into NO. Relaxation of the coordination sphere due to oxygen and NO adsorption, stability of C,N-containing intermediates and activation routes of hydrocarbons (methane, propane) were analyzed as factors determining catalytic properties of Cu and Co cations.     

Molecular Simulation on Competitive Adsorption Differences of Gas with Different Pore Sizes in Coal

Micropores are the primary sites for methane occurrence in coal. Studying the regularity of methane occurrence in micropores is significant for targeted displacement and other yield-increasing measures in the future. This study used simplified graphene sheets as pore walls to construct coal-structural models with pore sizes of 1 nm, 2 nm, and 4 nm. Based on the Grand Canonical Monte Carlo (GCMC) and molecular dynamics theory, we simulated the adsorption characteristics of methane in pores of different sizes. The results showed that the adsorption capacity was positively correlated with the pore size for pure gas adsorption. The adsorption capacity increased with pressure and pore size for competitive adsorption of binary mixtures in pores. As the average isosteric heat decreased, the interaction between the gas and the pore wall weakened, and the desorption amount of CH₄ decreased. In ultramicropores, the high concentration of CO₂ (50–70%) is more conducive to CH₄ desorption; however, when the CO₂ concentration is greater than 70%, the corresponding CH₄ adsorption amount is meager, and the selected adsorption coefficient S_CO2/CH4 is small. Therefore, to achieve effective desorption of methane in coal micropores, relatively low pressure (4–6 MPa) and a relatively low CO₂ concentration (50–70%) should be selected in the process of increasing methane production by CO₂ injection in later stages. These research results provide theoretical support for gas injection to promote CH₄ desorption in coal pores and to increase yield.     

Calculation of the molecular exchanging energy of binary surfactants system on the surface monolayer of aqueous solution

By using the binary anionic/cationic surfactants system CH3(CH2)nOSO_3/CH3(CH2)nN (CH3)3 as an ex-ample, the molecular exchanging energy (ε) of adsorption on the surface monolayer of aqueous solu-tion has been studied. ε can be obtained with two methods. One is from the relationship between ε and the molecule interaction parameter (β). This relationship is founded by considering that the adsorption of mixed surfactants on the surface monolayer of solution satisfies the dimensional crystal model condition under which β can be obtained by testing the surface tension of solution. The other is directly from the molecular structure of surfactants with the Lennard-Jones formula. The results for the studied system show that these two methods coincide well.