Implanting MnO2 into Hexagonal Boron Nitride as Nanoadditives for Enhancing Tribological Performance

Hexagonal boron nitride nanosheets (h-BNNs) show great potential in the field of tribology due to their typical two-dimensional layered structure and are essential for replacing conventional sulfur/phosphate-containing additives. However, the large particle size and poor dispersion of h-BNs seriously restrict their green lubrication application. In this paper, MnO2@h-BNNs nanocomposites were successfully prepared by ultrasonically exfoliating a hydrothermal method. The tribological properties of MnO2@h-BNNs nanocomposites as lubricant additives in poly-alpha-olefin oil (PAO) were investigated. The results show the oil dispersed with 0.25 wt% MnO2@h-BNNs had the best friction reduction and antiwear effect with 42% and 11.2% reduction, respectively, compared with the plain oil. Through further wear surface analyzing, we verified the antiwear mechanism of additives in filling the micropits and grooves on the wear surface and forming a friction protection film including Fe2O3, MnO2, and BN on the wear surface, avoiding direct contact between the friction subsets. This can provide ideas for other lubricating oil additives

Defect-Rich Heterogeneous MoS2/rGO/NiS Nanocomposite for Efficient pH-Universal Hydrogen Evolution

Molybdenum disulfide (MoS2) has been universally demonstrated to be an effective electrocatalytic catalyst for hydrogen evolution reaction (HER). However, the low conductivity, few active sites and poor stability of MoS2-based electrocatalysts hinder its hydrogen evolution performance in a wide pH range. The introduction of other metal phases and carbon materials can create rich interfaces and defects to enhance the activity and stability of the catalyst. Herein, a new defect-rich heterogeneous ternary nanocomposite consisted of MoS2, NiS and reduced graphene oxide (rGO) are synthesized using ultrathin αNi(OH)2 nanowires as the nickel source. The MoS2/rGO/NiS-5 of optimal formulation in 0.5 M H2SO4, 1.0 M KOH and 1.0 M PBS only requires 152, 169 and 209 mV of overpotential to achieve a current density of 10 mA cm−2 (denoted as η10), respectively. The excellent HER performance of the MoS2/rGO/NiS-5 electrocatalyst can be ascribed to the synergistic effect of abundant heterogeneous interfaces in MoS2/rGO/NiS, expanded interlayer spacings, and the addition of high conductivity graphene oxide. The method reported here can provide a new idea for catalyst with Ni-Mo heterojunction, pH-universal and inexpensive hydrogen evolution reaction electrocatalyst

Study on the mechanism of tunable ferromagnetic composites with different rare earth ions

Size-controlled Fe3O4 nanoparticles doped with rare earth (RE) ions (La3+, Ce3+, and Dy3+) varying from 15 nm to 30 nm were successful synthesized by a hydrothermal method for potential applications in the fields of biomedicine, environmental protection and magnetic memory devices. They possessed good dispersibility, adjustable particle size and nearly spherical shape. The particle grain size was uniformly distributed and showed a low degree of agglomeration in comparison with undoped Fe3O4 nanoparticles. The FTIR results showed that the RE elements partially replaced Fe2+, occupied the octahedral position, and enhanced the vibration of the Fe–O bond. The XPS study further revealed that the valence states of La, Ce, and Dy are both positive trivalent. The XPS Fe 2p valence band spectra observed a shift in the peak position toward higher binding energy after RE doping, confirming the existence of RE ions in the octahedral position. This paper explains the mechanism of rare earth doping with Fe3O4, and clarifies the influence of the doping of different RE ions on its magnetic properties. The detailed analysis of RE-doped ferrite materials can open a new perspective in designing biomedical and spintronics materials with tailored properties by choosing suitable cation substitution

Collaborative collection effort strategies based on “Internet + recycling” business model

"Internet + recycling", a new and emerging collecting mode, is booming in conjunction with widespread Internet use in China. For the recycling of waste electrical and electronic equipment (WEEE), this paper studies collaborative collection effort strategies in a collection system consisting of a third-party and an e-tailer based on the "Internet + recycling" business model. Considering the collaboration occurring during collecting and selling and mutual influences of partners on the recycling of old products, the paper applies collection effort cost sharing mechanisms to promote recycling. Four models, namely, the centralized model (C-Model), unit transfer price model (P-Model), unilateral cost sharing model (U-Model) and bilateral cost sharing model (B-Model), are established, and optimal decisions and members' profits in various collaborative models are derived and compared. The results show that there exists an interval of profit sharing proportions in which each of the two cost sharing models is a Pareto improvement of the P-Model, and the total collection volume and profit of the collecting system increase in the B-Model relative to those in the U-Model under the same proportion of profit sharing. However, the B-Model is not necessarily a Pareto improvement of the U-Model. The results also show that profit improvements of both parties can be achieved without the third-party sharing the e-tailer's collection effort cost in the B-Model when the collaborative marginal profit is large enough. The paper further explores the impact of the collaborative marginal profit and third-party's market influence on the total collection volume and the efficiency of the collecting system. This study provides insight into the promotion of WEEE recycling and into the selection of collaborative strategies for Internet recycling enterprises. The work will prove beneficial to the development of the WEEE "Internet + recycling" industry

Creación y Simulación de Metodologías de Análisis, Clasificación e Integración de Nuevos Requerimientos a Software Propietario

La priorización de nuevos requerimientos a implementar en un software propietario es un punto fundamental para su mantenimiento, la conservación de la calidad, observación de las reglas de negocio y los estándares de la empresa. Aunque existen herramientas de priorización basadas en técnicas probadas y reconocidas, las mismas requieren una calificación previa de cada requerimiento. Si la empresa cuenta con solicitudes provenientes de varios clientes de un mismo producto, aumentan los factores que afectan a la empresa, las herramientas disponibles no contemplan estos aspectos y hacen mucho más compleja la tarea de calificación. Este trabajo de investigación abarca la realización de un relevamiento de los métodos de priorización y selección de nuevos requerimientos utilizados por empresas de la zona de Rosario, y la definición de una metodología para la selección un nuevo requerimiento, que implica el análisis y evaluación de todas las implicaciones sobre el producto de software y la empresa, respetando sus reglas de negocio. La metodología creada conduce a la definición de los procesos para la construcción de una herramienta de calificación y priorización de nuevos requerimientos en software propietario que tiene solicitudes de varios clientes al mismo tiempo, con instrumentos de calificación que consideran todos los aspectos relacionados, proveerá técnicas de priorización actuales y emitirá informes personalizados según diferentes perspectivas de la empresa.Eje: Ingeniería de SoftwareRed de Universidades con Carreras en Informática (RedUNCI

Hippo signaling activates hedgehog signaling by Taz-driven Gli3 processing

Abstract The overlapping roles of Hippo and Hedgehog signaling in biological functions and diseases prompt us to investigate their potential interactions. Activation of Hippo signaling enhances the transcriptional output of Hedgehog signaling, and the role of Hippo signaling in regulating Hedgehog signaling relies on the Hippo pathway key effector, Taz. Interestingly, Taz exhibits a gradient expression across the posterior-to-anterior of limb bud mesoderms, similar to Sonic hedgehog (Shh). Importantly, Taz drives PKA to phosphorylate Gli3, resulting in the Gli3 processing into its repressor and attenuation of Hedgehog signaling in the Shh-independent manner. Specifically, Taz deletion in mouse embryonic limb bud mesenchyme not only enhances the Hedgehog signaling but partially restores the phenotypes from Shh deletion in causing severe defects of anteroposterior patterning and digit number and identity. Together, these results uncover Taz-dependent Gli3 processing as a hitherto uncharacterized mechanism controlling Hedgehog signaling, highlighting its cross-regulation by Hippo signaling

Interfacial construction of P25/Bi 2 WO 6 composites for selective CO 2 photoreduction to CO in gas–solid reactions

Photocatalysis provides an attractive approach to convert CO2 into valuable fuels, which relies on a well-designed photocatalyst with good selectivity and high CO2 reduction ability. Herein, a series of P25/Bi2WO6 nanocomposites were synthesized by a simple one-step in situ hydrothermal method. The formation of a heterojunction between Bi2WO6, which absorbs visible light, and P25, which absorbs ultraviolet light, expands the utilization of sunlight by the catalysts, and consequently, leads to a remarkably enhanced CO2 selective photoreduction to CO. The maximum CO yield of the P25/Bi2WO6 heterojunction under simulated solar irradiation was 15.815 μmol g−1 h−1, which was 4.04 and 2.80 times higher than that of pure P25 and Bi2WO6, respectively. Our investigations verified a Z-scheme charge migration mechanism based on various characterization techniques between P25 and Bi2WO6. Furthermore, in situ DRIFTS uncovered the related reaction intermediates and CO2 photoreduction mechanism. Our work sheds light on investigating the efficacious construction of Bi2WO6-based hybrids for light-driven photocatalysis

Activating Surface Lattice Oxygen of a Cu/Zn1–xCuxO Catalyst through Interface Interactions for CO Oxidation

Surface lattice oxygen in metal oxides is a common participant in many chemical reactions. Given this, the structural design of catalysts to activate lattice oxygen and moreover investigations into the effect of lattice oxygen on reaction pathways are hot topics. With this in mind, herein we prepare CuO–Zn1–xCuxO (ZCO) nanofibers akin to the Trojan horse legend and via an in situ reduction obtain activated Cu/Zn1–xCuxO (Cu/ZCO) nanofibers. X-ray absorption spectroscopy and X-ray photoelectron spectroscopy reveal that surface lattice oxygen of Cu/ZCO is effectively activated from inert O2– to reactive O2–x. This activation stems from the enhanced covalence of metal–oxygen bonds and the electron transfer between Cu and the support. Online mass spectrometry reveals that Cu/ZCO with activated lattice oxygen exhibits a higher Mars–van Krevelen reaction efficiency during the CO oxidation process. This study offers a new avenue to engineer interface interactions, given, as highlighted here, the importance of surface lattice oxygen in oxide supports during the catalytic process