Positively charged loose nanofiltration membrane grafted by diallyl dimethyl ammonium chloride (DADMAC) via UV for salt and dye removal

A novel positively charged loose nanofiltration (NF) membrane was fabricated feasibly by UV-induced photografting polymerization of diallyl dimethyl ammonium chloride (DADMAC) on Polysulfone ultrafiltration membrane. A possible reaction mechanism was proposed that a linear chain structure and/or pyrrole like five-membered nitrogen heterocycles structure on the side chain were grafted to form the active barrier layer. NF membrane demonstrated a looser average pore size of 8.6 nm and positive charges surface. Owing to the nanoscale ultrathin nanoscale barrier layer and the combination of Donnan exclusion and steric hindrance, NF membrane exhibited good hydrophilicity, a high pure flux of 60 L/m² h (0.5 MPa), a good salt rejection to Mg²⁺ (90.8%), Al³⁺ (94.0%), Ca²⁺ (91.5%), and a high dye rejection to methylene blue (99.4%) and congo red (100.0%) respectively. The salts rejection of NF membrane to different salts followed the order of AlCl₃ > CaCl₂ > MgCl₂ > NaCl > LiCl > MgSO₄ > Na₂SO_4. NF membrane showed certain fouling resistance to seawater and BSA solution. The grafting polymerization kinetics were comprehensively investigated including irradiation time, monomer concentration and irradiation intensity. X-ray Photoelectron Spectroscopy (XPS), scanning electron microscopy (SEM), atomic force microscopy (AFM) and contact angle measurement were employed to investigate membrane chemistry, morphologies, and hydrophilicity.     

The additive-free electrode based on the layered MnO2 nanoflowers/reduced,graphene oxide film for high performance supercapacitor

The MnO₂ nanoflowers/reduced graphene oxide composite is coated on a nickel foam substrate (denoted as MnO₂ NF/RGO @ Ni foam) via the layer by layer (LBL) self-assembly technology without any polymer additive, following the soft chemical reduction. The layered MnO₂ NF/RGO composite is uniformly anchored on the Ni foam skeleton to form the 3D porous framework, and the interlayers have access to lots of ions channels to improve the electron transfer and diffusion. This special construction of 3D porous structure is beneficial to the enhancement of electrochemical property. The specific capacitance is up to 246 F g⁻¹ under the current density of 0.5 A g⁻¹. After 1000 cycles, it can retain about 93%, exhibiting excellent cycle stability. The electrochemical impedance spectroscopy measurements confirm that MnO₂ NF/RGO @ Ni foam electrode has lower R_ESR and R_CT values when compared to MnO₂ @ Ni foam and RGO @ Ni foam. This study opens a new door to the preparation of composite electrodes for high performance supercapacitor.     

Fabrication of cylindrical SiCf/Si/SiC-based composite by electrophoretic deposition and liquid silicon infiltration

Cylindrical SiC-based composites composed of inner Si/SiC reticulated foam and outer Si-infiltrated SiC fiber-reinforced SiC (SiC_f/Si/SiC) skin were fabricated by the electrophoretic deposition of matrix particles into SiC fabrics followed by Si-infiltration for high temperature heat exchanger applications. An electrophoretic deposition combined with ultrasonication was used to fabricate a tubular SiC_f/SiC skin layer, which infiltrated SiC and carbon particles effectively into the voids of SiC fabrics by minimizing the surface sealing effect. After liquid silicon infiltration at 1550 °C, the composite revealed a density of 2.75 g/cm³ along with a well-joined interface between the inside Si/SiC foam and outer SiC_f/Si/SiC skin layer. The results also showed that the skin layer, which was composed of 81.4 wt% β-SiC, 17.2 wt% Si and 1.4 wt% SiO₂, exhibited a gastight dense microstructure and the flexural strength of 192.3 MPa.     

Graded Si3N4 ceramics with hard surface and tough core by two-step hot pressing

Graded Si₃N₄ ceramics with hard surface and tough core were prepared by two-step hot pressing with the homogenous starting composition. The inner Si₃N₄ layer was firstly hot-pressed at 1800 °C, subsequently covered with Si₃N₄ powders on both sides, and finally hot-pressed at 1600 °C. After two-step hot pressing, the resulting ceramics exhibited a zoned microstructure, differentiated by the phase assemblage of Si₃N₄ and grain size. The outer layers were well bonded to the inner layer. The outer layer exhibited bimodal and fine-grained microstructure, whereas the inner layer exhibited bimodal and coarse-grained microstructure. Vickers hardness of outer and inner layers were 18.1±0.2 GPa and 16.0±0.2 GPa, respectively, and fracture toughness were 4.2±0.1 MPa m^1/2 and 5.5±0.2 MPa m^1/2, respectively.     

Influence of the deposition energy on the composition and thermal cycling behavior of La2(Zr0.7Ce0.3)2O7 coatings

Lanthanum–zirconium–cerium composite oxide (La₂(Zr_0.7Ce_0.3)₂O₇, LZ7C3) coatings were prepared under different conditions by electron beam-physical vapor deposition (EB-PVD). The composition, crystal structure, surface and cross-sectional morphologies, cyclic oxidation behavior of these coatings were studied. Elemental analysis indicates that the coating composition has partially deviated from the stoichiometry of the ingot, and the existence of excess La₂O₃ is also observed. The optimized composition of LZ7C3 coatings could be effectively achieved by the addition of excess CeO₂ into the ingot or by properly controlling the deposition energy. Meanwhile, when the deposition energy is 1.15 × 10⁴–1.30 × 10⁴ J/cm², the coating has a similar X-ray diffraction (XRD) pattern to the ingot, and the thermal cycling life of the coating is also superior to other coatings. The spallation of the coatings occurs either within the ceramic layer approximately 6–10.5 μm above its thermally grown oxide (TGO) layer or at the interface between ceramic layer and bond coat.     

Diamond based field-effect transistors with SiNx and ZrO2 double dielectric layers

A diamond-based field-effect transistor (FET) with SiN_x and ZrO₂ double dielectric layer has been demonstrated. The SiN_x and ZrO₂ gate dielectric are deposited by plasma-enhanced chemical vapor deposition (PECVD) and radio frequency (RF) sputter methods, respectively. SiN_x layer is found to have the ability to preserve the conduction channel at the surface of hydrogen-terminated diamond film. The leakage current density (J) of SiN_x/ZrO₂ diamond metal-insulator-semiconductor FET (MISFET) keeps lower than 3.88 × 10^− 5 A·cm^− 2 when the gate bias was changed from 2 V to − 8 V. The double dielectric layer FET operates in a p-type depletion mode, whose maximum drain-source current, threshold voltage, maximum transconductance, effective mobility and sheet hole density are determined to be − 28.5 mA·mm^− 1, 2.2 V, 4.53 mS·mm^− 1, 38.9 cm²·V^− 1·s^− 1, and 2.14 × 10¹³ cm^− 2, respectively.     

ZrB2–SiC laminated ceramic composites

The oxidation behavior for ZrB₂–20 vol% SiC (ZS20) and ZrB₂–30 vol% SiC (ZS30) ceramics at 1500 °C was evaluated by weight gain measurements and cross-sectional microstructure analysis. Based on the oxidation results, laminated ZrB₂–30 vol% SiC (ZS30)/ZrB₂–25 vol% SiC (ZS25)/ZrB₂–30 vol% SiC (ZS30) symmetric structure with ZS30 as the outer layer were prepared. The influence of thermal residual stress and the layer thickness ratio of outer and inner layer on the mechanical properties of ZS30/ZS25/ZS30 composites were studied. It was found that higher surface compressive stress resulted in higher flexural strength. The fracture toughness of ZS30/ZS25/ZS30 laminates was found to reach to 10.73 MPa m^1/2 at the layer thickness ratio of 0.5, which was almost 2 times that of ZS30 monolithic ceramics.     

Growth and microstructure of Ba β-alumina films by laser chemical vapor deposition

Ba β-alumina films were prepared by laser chemical vapor deposition. Mostly single-phase Ba β-alumina films were obtained at 1125–1200 K and for an Al/Ba molar ratio of 12.4–16.6. BaAl₂O₄ and α-Al₂O₃ were codeposited with Ba β-alumina under Ba- and Al-rich conditions, respectively. The Ba β-alumina films consisted of hexagonal grains, and the (1 1 0)-oriented Ba β-alumina films had a fin-like columnar structure. The highest deposition rate reached 120 μm h^?1 at around 1200 K. A thin layer of Ba-rich superstructure was formed on the surface of the (1 1 0)-oriented columnar grains.     

Molten salt synthesis of titanate pyrochlore waste-forms

Actinide chlorides, such as those arising from pyrochemical reprocessing operations can be problematic to immobilise, as the high chloride content often makes their solubilities in melts very low, and even in small quantities can seriously affect the properties of the waste-form. Rather than attempt to immobilise the chlorine, one potential approach is to utilise the chloride salt as a reaction medium from which the An(III) cations can be extracted and immobilised. To this end, lanthanide titanate pyrochlores have been prepared by molten salt synthesis in CaCl₂:MgCl₂, CaCl₂:NaCl and MgCl₂:NaCl eutectics. Single-phase pyrochlore is found to be formed at temperatures as low as 650 °C in the CaCl₂:NaCl system, whereas in the CaCl₂:MgCl₂ and MgCl₂:NaCl eutectics reaction with Mg produces a magnesium titanate secondary phase. Compositions of Yb₂Ti₂O₇ doped with Sm³⁺ as an actinide surrogate have been synthesised, and cold-pressing and sintering at 1500 °C yields fully dense pellets.     

Synthesis and catalytic properties of novel POM@TiO2 composite materials

Donor–π-bridge–acceptor (D–π–A) type polyoxometalates (POMs) were self-assembled for the first time on the surface of titanium dioxide (TiO₂) nanoparticles through the layer-by-layer (LBL) method. The obtained composite materials POM@TiO₂ were characterized by Transmission electron microscopy (TEM), Fourier transform IR spectroscopy (FTIR), Raman spectrum and energy dispersive X-ray (EDX) spectroscopy. Catalytic properties of POM@TiO₂ were also investigated by treating organic pollutants (typically, removal of 40 mL 20 mg L^− 1 methylene blue (MB) by 10 mg POM@TiO₂ was up to 99.5% within 3 min under ambient conditions and the photodegradation efficiency was obviously higher than bare TiO₂ nanoparticles under irradiation).     

New morphological Ba0.5Sr0.5Co0.8Fe0.2O3−α hollow fibre membranes with high oxygen permeation fluxes

Perovskite Ba_0.5Sr_0.5Co_0.8Fe_0.2O_3?α (BSCF) hollow fibre membranes were fabricated by a combined phase inversion and sintering technique. The membranes were characterised by XRD, SEM and tested for air separation. The membrane possesses a novel morphology consisting of one dense layer and one porous layer. Oxygen permeation fluxes through the obtained hollow fibre membranes were measured in the temperature range 650–950 °C using helium sweep gas rates from 50 to 200 mL min^?1. Experimental results indicated the oxygen permeation flux through the BSCF hollow fibre membrane sintered at 1050 °C was approximately 11.46 mL min^?1 cm^?2 at 950 °C when the helium sweep rate was kept at 200 mL min^?1. The BSCF hollow fibre membrane showed a stable oxygen permeation flux of 8.60 mL min^?1 cm^?2 over the investigated period of 120 h at 900 °C.     

Kilohertz ultrafast electrochemical supercapacitors based on perpendicularly-oriented graphene grown inside of nickel foam

Ultrafast electrochemical supercapacitors (EC) that can work at or above kilohertz (kHz) frequency, 3–4 orders higher than traditional EC, call for a structure with extremely low equivalent serial resistance (ESR) and a reasonably large surface area. Three-dimensional perpendicularly-oriented graphene (POG) network, grown inside of Ni foam (NF) by microwave plasma chemical vapor deposition, is reported as electrode to fabricate such ultrafast EC. The folded POG inside NF provides a large surface area, while the straight-forward and wide-open porous structure of POG ensures fast ion migration. In conjunction with the intrinsic high electronic conductivity of graphene and Ni, POG/NF electrode based ultrafast EC was demonstrated with a specific cell capacitance of 0.32 mF/cm² at 1 kHz, a relaxation time constant of 0.248 ms, and an ESR of 70 mΩ. A charge–discharge rate as high as 500 V/s was also measured, at which the cyclic voltammogram maintained a rectangular shape, corresponding to a single electrode capacitance of 0.83 mF/cm².     

Polyphosphates used for membrane scaling inhibition during water desalination by membrane distillation

The desalination of surface water (lake) was performed using direct contact membrane distillation. The membrane distillation process was carried out at 358 K. As a consequence of water heating the CaCO₃ deposit formed on the membrane surfaces, which resulted in a decrease in module efficiency. The polyphosphate antiscalant was used for restriction of carbonate deposition. In order to increase the scaling potential during the desalination process, the water was additionally enriched with bicarbonates (feed alkalinity 3.1 mmol HCO₃^–/dm³ and 4.5 mmol HCO₃^–/dm³). The membrane distillation with and without antiscalant was carried out to evaluate the scale inhibition effect. Various solution compositions (2–20 ppm) of the commercial polyphosphate based antiscalant (destined for reverse osmosis) and laboratory-grade sodium polyphosphate was used. SEM–EDS was used to investigate the chemical composition and morphology of the precipitate formed on the membrane surface. It was found that the formation of CaCO₃ crystallites was almost eliminated as a result of using antiscalant. However, a thin layer of amorphous deposits on the membrane surface was observed. As a results, a decline of the permeate flux was still observed. The initial module efficiency was restored by periodical rinsing of the membranes with diluted HCl solutions. The application of antiscalant minimized the penetration of deposit into the pores, and a high permeate flux was maintained over a period of 260 h of performed investigations when periodical rinsing with HCl solution was used.     

A hydrogen-permselective amorphous silica membrane derived from polysilazane

A microporous amorphous silica membrane has been synthesized by thermal conversion in air of polysilazane on a silicon nitride (Si₃N₄) porous substrate. The porous substrate near the surface layer was penetrated by polysilazane, and converted into mesoporous amorphous silica/Si₃N₄ composite layer. Then, an active molecular sieving microporous amorphous silica thin layer was synthesized on the surface of the mesoporous composite layer. The polysilazane-derived amorphous silica membrane exhibited H₂ permeance of 1.3 × 10⁻⁸ mol/m² s Pa at 573 K, and the permeability ratio of H₂/N₂ was measured to be 141. The effects of heat treatment condition on the meso/microporous structure development of the polysilazane-derived amorphous silica within the Si₃N₄ porous substrate are discussed from a viewpoint of fabricating hydrogen-permselective amorphous silica membranes through polymeric precursor route.     

Effect of support synthesis methods on structure and performance of VOx/CeO2 catalysts in low-temperature NH3-SCR of NO

CeO₂ supports were prepared by a citrate (C) or a precipitation method (P) before deposition of vanadia by wet impregnation to obtain supported V/CeO₂ catalysts. The V/CeO₂-P catalyst is more active, reaching ≈ 100% NO conversion and N₂ selectivity already below 225 °C at a space velocity of GHSV = 70,000 h^− 1. XRD, UV-vis-DRS, Raman, pseudo-in-situ-XPS and operando-EPR spectroscopy revealed that this is due to higher surface area and a more effective incorporation of V sites into the support surface, which keeps them in their active valence states + 5 and + 4 and prevents reduction to inactive V^3 + as observed on V/CeO₂-C.     

Tribological characterization of NCD in physiological fluids

NCD films deposited on silicon nitride (Si₃N₄) ceramic substrates by hot-filament chemical vapour deposition (HFCVD) technique were biotribologically assessed under lubrication of Hank's balanced salt solution (HBSS) and dilute fetal bovine serum (FBS), using a pin-on-flat test configuration. The reciprocating tests were conducted under an applied load of 45 N during 500,000 cycles using a NCD coated Si₃N₄ biocompatible ceramic substrates with two different surface preparations: i) polished (P) and ii) polished and plasma etched (PE). Friction coefficient values of 0.02 and 0.12 were measured for the P samples under HBSS and FBS lubrication, respectively. PE samples showed increased adhesion relatively to P ones and withstood 6 km of sliding distance without any evidence of film fracture but with friction coefficients of 0.06 for HBSS and 0.10 for FBS experiments. Evidences of protein attachment and salt deposition were found, being the responsible for the enhancement of friction under FBS relatively to HBSS. The wear rates measured for the NCD films are in the range of ~10^− 9–10^− 8 mm³·N^− 1m^− 1, values that are similar to the best values found for ceramic-on-ceramic combinations.     

Effect of the surface microstructure of SiC inner coating on the bonding strength and ablation resistance of ZrB2-SiC coating for C/C composites

The present study has been conducted in order to investigate the effect of the surface morphology of SiC inner coating on the bonding strength and ablation resistance of the sprayed ZrB₂-SiC coating for C/C composites. The microstructure of SiC inner coatings prepared by chemical vapor deposition and pack cementation at different temperatures were analyzed by X-ray diffraction, scanning electron microscopy, and 3D Confocal Laser Scanning Microscope. Tensile bonding strength and oxyacetylene ablation testing were used to characterize the bonding strength and ablation resistance of the sprayed ZrB₂-SiC coating, respectively. Results show that SiC inner coating prepared by chemical vapor deposition has a smooth surface, which is not beneficial to improve the bonding strength and ablation resistance of the sprayed ZrB₂-SiC coating. SiC inner coating prepared by pack cementation at 2000 °C has a rugged surface with the roughness of 72.15 µm, and the sprayed ZrB₂-SiC coating with it as inner layer exhibits good bonding strength and ablation resistance.     

Fast discharge and high energy density of nanocomposite capacitors using Ba0.6Sr0.4TiO3 nanofibers

Nanocomposites combining high breakdown strength (BDS) polymer and high dielectric permittivity ceramic fillers have shown great potential for pulsed power application. Here a new composite material based on surface-functionalized Ba_0.6Sr_0.4TiO₃ nanofibers/poly(vinylidene fluoride) (BST NF/PVDF) has been prepared by solution casting. The nanocomposites containing 2.5 vol% isopropyl dioleic(dioctylphosphate) titanate (NDZ 101)-functionalized BST NF (N-h-BST NF) have large energy density of 6.95 J cm⁻³ at 380 MV m⁻¹, which is 1.85 times larger than that of the pure PVDF at the same electric field. Also, the discharge speed of the nanocomposites containing 7.5 vol% N-h-BST NF is approximately 0.11 μs. The good properties, together with the large energy density and fast discharge speed, make this material a promising candidate for pulsed power capacitor.     

Transparent and high infrared reflection film having sandwich structure of SiO2/Al:ZnO/SiO2

New transparent and high infrared reflection films having the sandwich structure of SiO₂/Al:ZnO(AZO)/SiO₂ were deposited on the soda-lime silicate glass at room temperature by radio frequency (R.F.) magnetron sputtering. The optical and electrical properties of SiO₂ (110 nm)/AZO (860 nm)/SiO₂ (110 nm) sandwich films were compared with those of single layer AZO (860 nm) films and double layer SiO₂ (110 nm)/AZO (860 nm) films. The results show that these sandwich films exhibit high transmittance of over 85% in the visible light range (380–760 nm), and low reflection rate of below 4.5% in the wavelength range of 350–525 nm, which is not shown in the conventional single layer AZO (860 nm) films and double layer SiO₂ (110 nm)/AZO (860 nm) films. Further these sandwich films display a low sheet resistance of 20 Ω/sq by sheet resistance formula and high infrared reflection rate of above 80% in the wavelength range of 15–25 μm. In addition, the infrared reflection property of these sandwich films is determined mainly by the AZO film. The outer SiO₂ film can diminish the interference coloring and increase transparency; the inner SiO₂ film improves the adhesion of the coating to the glass substrate and prevents Ca²⁺ and Na⁺ in the glass substrate from entering the AZO film.     

Oxygen permeation through dense La0.1Sr0.9Co0.8Fe0.2O3−δ perovskite membranes: Catalytic effect of porous La0.1Sr0.9Co0.8Fe0.2O3−δ layers

The oxygen permeation performance of a number of La_0.1Sr_0.9Co_0.8Fe_0.2O_3−δ (LSCF1982)-based membranes, consisting of dense LSCF1982 layer with/without porous LSCF1982 layer, was analyzed on the basis of the thickness of the dense layer and catalytic effect of the porous layer. A 0.27 mm thick dense membrane gives oxygen permeation flux ($J_{O_2}$) of 2.33 sccm min⁻¹ cm⁻² at 900 °C, which is increased to 3.55 sccm min⁻¹ cm⁻² on applying a porous layer of LSCF1982 onto the dense membrane. The membrane gives a stable flux for 300 h. The flux was further improved by reducing the thickness of the dense LSCF1982 layer and at 950 °C a flux of 4.47 sccm min⁻¹ cm⁻² is obtained with 0.012 mm thick membrane.