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Through nanoscratch experiments with a spherical diamond indenter, a contrastive study of the nanotribological properties of Ga- and N-faced gallium nitride (GaN) samples was carried out. Nanoindentation results revealed that the elastic modulus of the Ga-faced GaN sample was slightly higher than that of N-faced GaN sample. Particularly, Ga- and N-faced GaN samples exhibited rather different nanotribological properties, and the Ga-faced sample showed a stronger wear resistance. The study indicated that the critical normal load required to cause material removal of N-faced GaN sample was almost two times that of Ga-faced GaN sample. Both Ga- and N-faces exhibited a rather low frictional coefficient at the elastic and elastoplastic stages of material, e.g., ~0.06 for Ga-face and ~0.075 for N-face when scratching under the progressive normal load. Combined with transmission electron microscopy and X-ray photoelectron spectroscopy, we speculated that, except for the intrinsic atomic arrangements attributed to the non-reverse crystallographic symmetry of c-plane wurtzite GaN, the difference of nanotribological properties between Ga- and N-faces may also be related to the preferential formation of a native oxide layer and a slight lattice damage layer on the N-faced GaN surface. This study can enrich the understanding of the nanotribological properties of Ga- and N-polar-faced bulk monocrystalline GaN materials fabricated by the conventional technique. [ABSTRACT FROM AUTHOR]

The aim of this study was to optimize the adsorption performance of activated carbon (AC), derived from the shell of Penaeus vannamei prawns, on heavy metal ions. Inexpensive, non-toxic, and renewable prawn shells were subjected to carbonization and, subsequently, KOH-activation to produce nanoporous K-Ac. Carbonized prawn shells (CPS) and nanoporous KOH-activated carbon (K-Ac) from prawn shells were prepared and characterized by FTIR, XRD, BET, SEM, and TEM. The results showed that as-produced K-Ac samples were a porous material with microporous and mesoporous structures and had a high specific surface area of 3160 m2/g, average pore size of about 10 nm, and large pore volume of 2.38 m3/g. Furthermore, batches of K-Ac samples were employed for testing the adsorption behavior of Cd2+ in solution. The effects of pH value, initial concentration, and adsorption time on Cd2+ were systematically investigated. Kinetics and isotherm model analysis of the adsorption of Cd2+ on K-Ac showed that experimental data were not only consistent with the Langmuir adsorption isotherm, but also well-described by the quasi-first-order model. Finally, the adsorption behaviors of as-prepared K-Ac were also tested in a ternary mixture of heavy metal ions Cu2+, Cr6+, and Cd2+, and the total adsorption amount of 560 mg/g was obtained. [ABSTRACT FROM AUTHOR]

Using an atomic force microscope (AFM), the wear of monocrystalline silicon (covered by a native oxide layer) at high humidity was investigated. The experimental results indicated that tribochemistry played an important role in the wear of the silicon at different relative humidity levels (RH = 60%, 90%). Since the tribochemical reactions were facilitated at 60% RH, the wear of silicon was serious and the friction force was around 1.58 μN under the given conditions. However, the tribochemical reactions were restrained when the wear pair was conducted at high humidity. As a result, the wear of silicon was very slight and the friction force decreased to 0.85 μN at 90% RH. The slight wear of silicon at high humidity was characterized by etching tests. It was demonstrated that the silicon sample surface was partly damaged and the native oxide layer on silicon sample surface had not been totally removed during the wear process. These results may help us optimize the tribological design of dynamic microelectromechanical systems working in humid conditions. [ABSTRACT FROM AUTHOR]

X-ray diffraction (XRD) analysis showed that metal oxide peaks appear at 2θ = 47.7°, 54.5°, and 56.3°, corresponding to Yb2O3 (440), Co2O3 (422), and Co2O3 (511). It was found that oxide formation plays an important role in magnetic, electrical, and surface energy. For magnetic and electrical measurements, the highest alternating current magnetic susceptibility (χac) and the lowest resistivity (×10−2 Ω·cm) were 0.213 and 0.42, respectively, and at 50 nm, it annealed at 300 °C due to weak oxide formation. For mechanical measurement, the highest value of hardness was 15.93 GPa at 200 °C in a 50 nm thick film. When the thickness increased from 10 to 50 nm, the hardness and Young's modulus of the Co60Fe20Yb20 film also showed a saturation trend. After annealing at 300 °C, Co60Fe20Yb20 films of 40 nm thickness showed the highest surface energy. Higher surface energy indicated stronger adhesion, allowing for the formation of multilayer thin films. The optimal condition was found to be 50 nm with annealing at 300 °C due to high χac, strong adhesion, high nano-mechanical properties, and low resistivity. [ABSTRACT FROM AUTHOR]

Our work proposes a comparison between Spark Plasma Sintering of LiFePO4 carried out using an Alternating Current (AC) and Direct Current (DC). It quantifies the Li-ion migration using DC, and it validates such hypothesis using impedance spectroscopy, X-ray photoelectron spectroscopy and inductively coupled plasma optical emission spectroscopy. The use of an AC field seems effective to inhibit undesired Li-ion migration and achieve high ionic conductivity as high as 4.5 × 10−3 S/cm, which exceeds by one order of magnitude samples processed under a DC field. These results anticipate the possibility of fabricating a high-performance all-solid-state Li-ion battery by preventing undesired Li loss during SPS processing. [ABSTRACT FROM AUTHOR]

The friction weldability of Ti-45Al-8.5Nb-0.2W-0.2B-0.02Y alloy has been investigated by optimizing process parameters and analyzing the microstructures and tensile properties of the joints. The as-cast alloy with a nearly lamellar (NL) microstructure and the as-forged alloys with a duplex (DP) microstructure have been successfully welded. All the joints have a severe deformation zone (SDZ) and a transition zone (TZ) between the parent metal (PM) and SDZ. SDZ, showing a biconcave lens geometry, has a maximum thickness of hundreds of micrometers at the periphery. TZ is hundreds of micrometers thick. All SDZs have a fine-grained DP microstructure with a grain size of a few micrometers. For the joint of the as-cast alloy, the TZ consists of deformed lamellar colonies as the major constituent and partially recrystallized grains as the minor constituent. For the joint of the as-forged alloy, the TZ is similar to both the PM and SDZ, showing a DP microstructure. The grain size, volume fraction of γ grains, and the remnant lamellar colonies all increase with the distance from the SDZ. All joints presented perfect metallurgical bonding. The strengths of the joints are higher than those of the corresponding PMs. This indicates that the studied alloy has good friction weldability. [ABSTRACT FROM AUTHOR]

A certain amount of ferroaluminate cement (FAC) was substituted for MgO during the magnesium phosphate cement (MPC) preparation to obtain the MPC–FAC composite cement. The influence of FAC on the strength, water resistance, pH, and setting time of MPC–FAC composite cement were examined. The microstructure and chemical composition were also analyzed by adopting scanning electron microscopic energy-dispersive spectrometer and X-ray diffraction, respectively. The study showed that setting time of MPC–FAC composite cement was dramatically prolonged when FAC substitution for MgO was between 30 and 40 wt %. The strength of MPC–FAC did not decrease during the early curing time (1 h and 1 d), whereas it increased during the late curing time (3, 7, and 28 days). Moreover, the existence of FAC decreased the hydrated product K-struvite during the early curing time and thus dramatically enhanced the water-resistance of MPC–FAC. With the addition of FAC, a large number of cementitious materials of AFt and AFm, as well as flocculent colloidal substances of AH3, C–S–H, and FH3, were generated during the hydration of MPC, which were filled in the internal pore of the hydrate. Thus, the internal compactness of the sample increased, while the compact protective covering layer was generated on the surface to enhance the water resistance and strength in the late curing time. [ABSTRACT FROM AUTHOR]

With the assistance of surfactant, Fe nanoparticles are supported on g-C3N4 nanosheets by a simple one-step calcination strategy. Meanwhile, a layer of amorphous carbon is coated on the surface of Fe nanoparticles during calcination. Transmission electron microscopy (TEM), scanning electron microscope (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma (ICP) were used to characterize the morphology, structure, and composition of the catalysts. By electrochemical evaluate methods, such as linear sweep voltammetry (LSV) and cyclic voltammetry (CV), it can be found that Fe25-N-C-800 (calcinated in 800 °C, Fe loading content is 5.35 wt.%) exhibits excellent oxygen reduction reaction (ORR) activity and selectivity. In 0.1 M KOH (potassium hydroxide solution), compared with the 20 wt.% Pt/C, Fe25-N-C-800 performs larger onset potential (0.925 V versus the reversible hydrogen electrode (RHE)) and half-wave potential (0.864 V vs. RHE) and limits current density (2.90 mA cm−2, at 400 rpm). In 0.1 M HClO4, it also exhibits comparable activity. Furthermore, the Fe25-N-C-800 displays more excellent stability and methanol tolerance than Pt/C. Therefore, due to convenience synthesis strategy and excellent catalytic activity, the Fe25-N-C-800 will adapt to a suitable candidate for non-noble metal ORR catalyst in fuel cells. [ABSTRACT FROM AUTHOR]

In this study, modified activated fishbone charcoal (MAFC) was successfully prepared to remove emulsified oil from oily wastewater. Various characteristic techniques, including SEM, XRD, FTIR, and BET, were employed to investigate the morphology, texture, and surface properties of as-prepared samples. BET results demonstrated that the specific surface area of fishbone charcoal increased from 69.8 m2/g to 206.0 m2/g after treatment with K2CO3 as an activating agent, while the total pore volume of MAFC increased from 0.003 cm3/g to 0.3 cm3/g, accompanied by the formation of abundant pore structures. It was observed that 90.1% of emulsified oil (100 mg/L) was successfully removed by MAFC under our experimental conditions. The results of a kinetic and isotherm model analysis indicated that the adsorption experimental data were not only consistent with the Langmuir adsorption isotherm but were also well-described by the pseudo-second-order adsorption model. It is expected that this highly efficient and inexpensive MAFC can be a promising bio-adsorbent for removing organic pollutants from industrial wastewater. [ABSTRACT FROM AUTHOR]

In this study, carbonized kelp biochar (AKB) modified by KOH impregnation and photocatalytic Bi2MoO6/AKB composite (BKBC) nanomaterials were the first time successfully synthesized for efficient removal of dyes in aqueous solution. BET, XRD, FT-IR, and SEM were employed to characterize as-prepared samples. UV-vis and other test results indicated that the removal efficiency of methylene blue (MB) was 61.39% and 94.12% for BKBC and AKB, respectively, which was up to 13 times and 20 times higher in comparison with pure Bi2MoO6 (PBM). In addition, the equilibrium adsorption capacity of MB could reach up to 324.1 mg/g for AKB. This high dyes adsorption performance could be likely attributed to its high specific surface area (507.177 m2/g) and its abundant presence of various functional groups such as –OH and =C–H on AKB. Particularly, the existing of amorphous carbon and transition metal oxides, such as Fe2O3 and Mn5O8, could be beneficial for the photodegradation of MB for AKB. Meanwhile, experimental data indicated that adsorption kinetics complied with the pseudo-second order model well, and all of the tests had satisfactory results in terms of the highly efficient adsorption and photodegradation activity of AKB nanomaterials, which suggested its great potential in wastewater treatment. [ABSTRACT FROM AUTHOR]

Biomass is known to efficiently adsorb pollutants from wastewater. In this paper, we demonstrated that a new antistatic oil-cleaning material can be prepared and assembled by using two surfactants, alkyl polyglucosides (APG) and dimethyl octadecyl hydroxy ethyl ammonium nitrate (SN), to modify calcined mussel shell powder (CMSP) through a two-step hydrotherm-assisted adsorption. The pore size and structure of CMSP was measured by BET and a contact angle meter was used to characterize the surface wetting ability. XRD, FTIR, XPS, SEM, TEM, and HRTEM were employed to determine the surface structure of CMSP modified by surfactants APG and SN (MMO). In order to further characterize properties of the surface morphology and crystal structure, the HRTEM was employed to show that the MMO surface had a single crystal structure: calcite, with a crystal plane spacing of 0.2467 nm. The surface of MMO appeared to be fluffy and disperse. The antistatic and degreasing ability of as-prepared samples (MMO) was evaluated by a ZC-36 high resistance meter and BD-457 whiteness meter. The results showed that when the calcination temperature of CMSP reached 1000 °C, and the addition amount of APG and SN was 0.8 g and 0.16 g, it had an optimum antistatic effect with a surface resistivity (Rs) of 1.35 × 108 Ω, and a detergency rate to oil of 17.35%. This study aims to embrace a green solution to reduce environmental pressure and make use of waste, which is of great significance to environmental protection. [ABSTRACT FROM AUTHOR]