Fabrication and performances of high lithium-ion conducting solid electrolytes based on NASICON Li1.3Al0.3Ti1.7-xZrx(PO4)3 (0≤ x≤ 0.2)

Solid electrolytes are the key component in designing all-solid-state batteries. The Li_1.3Al_0.3Ti_1.7(PO₄)₃ (LATP) structure and its derivatives obtained by doping various elements at Ti and Al site acts as good solid electrolytes. However, there is still scope for enhancing the ionic conductivity using simple precursors and preparation methods. In this study, the Li superionic conductors Li_1.3Al_0.3Ti_1.7-xZr_x(PO₄)₃ (LATZP) with 0 ≤ x ≤ 0.2 have been successfully prepared by the solid-state reaction route. The structural, morphological, and ionic transport properties were analyzed using several experimental techniques including powder X-ray diffraction (XRD), scanning electron microscopy (SEM), and impedance spectroscopy (IS). The presence of two relaxation processes corresponding to grain and grain boundary was studied using various formalisms. We have observed that grain effects dominate at lower temperatures (<100 °C) while the grain boundary at higher temperatures (> 200 °C) on ionic conductivity. The relaxation mechanisms of grain and grain boundaries were investigated by the Summerfield scaling of AC conductivity. The highest total ionic conductivity of 2.48 × 10^-4 S/cm at 150 °C and 5.50 × 10^-3 S/cm at 250 °C was obtained for x = 0.1 in Li_1.3Al_0.3Ti_1.6Zr_0.1(PO₄)₃ sintered at 950 °C/6 h in the air. The ionic conductivity value was found to be higher than the ionic conductivity reported for LATP prepared via solid-state reaction mechanism using the same precursors and conditions.     

A modified cross-correlation algorithm for PIV image processing of particle-fluid two-phase flow

PIV (Particle Image Velocimetry) technique for flow field measurement has achieved popular self-identify through over ten years development, and its application range is becoming wider and wider. PIV post-processing techniques have a great influence on the success of particle-fluid two-phase flow field measurement and thus become a hot and difficult topic. In the present study, a Phase Respective Identification Algorithm (PRIA) is introduced to separate low-density solid particles or bubbles and high-density tracer particles from the PIV image of particle-fluid two-phase flow. PTV (Particle Tracking Velocimetry) technique is employed to calculate the velocity fields of low-density solid particles or bubbles. For the velocity fields of high-density solid particles or bubble phase and continuous phase traced by high-density smaller particles, based on the thought of wavelet transform and multi-resolution analysis and the theory of cross-correlation of image, a delaminated processing algorithm (MCCWM) is presented to conquer the limitation of conventional Fourier transform. The algorithm is firstly testified on synthetic two-phase flows, such as uniform steady flow, shearing flow and rotating flow, and the computational results from the simulated particle images are in reasonable agreement with the given simulated data. The algorithm is then applied to images of actual bubble-liquid two-phase flow and jet flow, and the results also confirmed that the algorithm proposed in the present study has good performance and reliability for post-processing PIV images of particle-fluid two-phase flow.     

Postural strategy identification during drilling task for different materials and heights: Ergonomic risk assessment

Drilling is an activity carried out in both professional and domestic environments. In this context, knowing the postural strategies used by users is a challenge. The objective of this study is twofold: 1) to identify the different possible strategies for performing a piercing while characterizing them through quantitative biomechanical parameters related to the task; 2) to propose an evaluation of the ergonomic risks incurred by the users for each of the observed strategies. Thus, fourteen subjects carried out a drilling activity at two different heights and for two types of materials. The position of the gravity center projection in relation to the sustentation polygon as well as the angle between the axis connecting the two feet and the antero-posterior axis (drilling axis) were used to identify the different postural strategies. Three strategies respectively called “Inter-feet”, “Left foot” and “External strategy” and three sub-strategies were identified. Each has been characterized through the duration and the average and maximum forces applied during the drilling phase. Two of them, 0–30° and 30–60° Inter-feet strategies covered about 75% of the trials. Despite the presence of a lower score for the 30–60° and 60–90° External strategies, the ergonomic analysis through the Rapid Upper Limb Assessment revealed that regardless of the strategy used, the postures adopted presented risks of developing musculoskeletal disorders. Thus, the drilling activity must be considered with care.Relevance to industryThe identification and characterization of postural strategies is particularly interesting to better understand the organization of the drilling task and thus optimize productivity while ensuring operator safety.     

Tungsten-based heterogeneous multilayer structures via diffusion bonding

Recent work has shown that tungsten (W) and other refractory metals with body-centered cubic (bcc) structures exhibit certain novel behavior when their grain size, d, is refined into the ultrafine (UFG, 100 nm < d < 1000 nm) or nanocrystalline (NC, d < 100 nm) regime. For example, it has been shown that bcc refractory metals with such microstructures show decreased strain rate sensitivity besides their elevated strength and vanishing strain hardening response. Consequently, under both quasi-static and high-strain-rate loading, plastic instability in the form of shear banding becomes the dominant mode of plastic deformation. Such behavior is long sought-after in certain applications. However, due to the technology used to refine the grain size (primarily severe plastic deformation), the inability to scale the dimensions of the material may limit wider use and application of UFG/NC bcc refractory metals. In this work, the feasibility was demonstrated of production of large-scale W parts using a diffusion bonding method. The microstructure, preliminary mechanical properties, and issues and challenges associated with the fabrication procedures were examined and discussed. It is envisioned that diffusion bonding may serve as a promising technology for scaled-up fabrication of UFG bcc refractory metals for the targeted application.     

A size-dependent thermodynamic model for coke crystallites: The carbon–hydrogen system up to 2500 K

The development is presented of a model of the thermodynamic functions of enthalpy, entropy and Gibbs energy for the elements carbon and hydrogen in coke crystallites. It is applicable to varying degrees of graphitization, described by the crystallite length L_a and the crystallite height L_c. The model parameters are derived from known properties such as bond enthalpies and entropies of formation. Good agreement has been obtained between the predicted thermal dehydrogenation of petroleum cokes and experimental data. The removal of hydrogen from idealized coke crystallites is predicted to occur mostly between 1100 and 1300 K. Agreement has also been found in the comparison of the predicted thermodynamic stability of coke relative to graphite, in a previous experimental study. This stability has been determined as at ≈900 J g⁻¹ at temperatures between 950 and 1250 K and for L_a = 10 nm. The current predictive capacity of the present model is valid for temperatures up to 2500 K.     

Collapse load of composite laminates: Lower bound evaluation by stress field analytical approximation

The paper proposes a limit analysis approach to define the ultimate load capacity of orthotropic composite laminates under biaxial loading and plane stress conditions. A lower bound to the collapse load multiplier is computed by solving a maximization nonlinear problem, according to the static theorem of limit analysis. To set up the optimization problem a stress field distribution is hypothesized at lamina level, moreover inter-lamina stresses are also considered. The effectiveness and validity of the proposed approach is shown by comparing the obtained numerical predictions both with available experimental data and with other numerical results carried out by means of a different numerical lower bound approach.     

Ag–Cu–BTC prepared by postsynthetic exchange as effective catalyst for selective oxidation of toluene to benzaldehyde

A mixed-node MOF catalyst Ag–Cu–BTC was prepared by postsynthetic exchange (PSE) method. It is believed that PSE method can realize isomorphous replacement of Ag ion to framework Cu ion in Cu–BTC successfully. The catalytic performance of Ag–Cu–BTC was investigated via selective oxidation of toluene to benzaldehyde by molecular oxygen in the absence of solvent and initiator. This catalyst exhibits good catalytic performance: on the premise of keeping highly selective catalysis of Cu–BTC for toluene oxidizing to benzaldehyde, the introduction of Ag (Ag content is 2.76 wt.%) can promote toluene conversion from 6.5% to 12.7%.     

A novel Zn6Co3 cluster-based heterometallic coordination polymer with PMG3 − linker formed via in situ decarboxylation from H4PMIDA

A novel Zn₆Co₃ cluster-based heterometallic coordination polymer, [Zn₆Co₃(PMG)₆(H₂O)₄]·12H₂O (1), has been hydrothermally synthesized, in which the PMG^3 − (N-(phosphonomethyl)glycinate) as a multifunctional ligand was firstly formed via in situ decarboxylation from original ligand N-(phosphonomethyl)imino-diacetic acid during the hydrothermal reaction. The complex was characterized by elemental analysis, FT-IR, powder X-ray diffraction, thermal analysis and single-crystal X-ray diffraction techniques. Its structure features a 2D framework constructed by [Zn₆Co₃(PMG)₆(H₂O)₄] pinwheel-like heteronuclear clusters, which contains rings with two tropisms. Through extensive O–H⋯O hydrogen bondings, the adjacent 2D layered structure further extends into a 3D supramolecular network. Moreover, the solid-state fluorescence property of this complex has also been investigated at room temperature, which exhibits a good fluorescent emission.     

Understanding value creation in closed loop supply chains – Past findings and future directions

The topic of value creation through the recovery of returned products in closed loop supply chains is scattered across various bodies of literature. We undertake a systematic literature review of 144 articles in relevant green, reverse and closed loop supply chain literature to synchronize existing knowledge on value creation. Value manifestations of four types of value, namely economic, environmental, information and customer value, are identified. Value adding concepts from the forward- and reverse supply chain may leverage the process of value creation. They are classified into six subclasses, namely partnerships and collaboration, product design characteristics, service concepts, IT solutions, supply chain processes and organizational characteristics. We present a conceptual framework on a strategic level. In this way companies can create competitive advantages by closing the loop. The results of the literature analysis suggest avenues for future research on the operational and strategic level.     

Enhancing cation exchange capacity of chars through ozonation

The use of ozone to increase the cation exchange capacity (CEC) of two chars produced from pyrolysis of Douglas fir (Pseudotsuga menziessii) and a control bituminous coal activated carbon (AC) is reported. Chars were produced from the wood fraction of Douglas fir (DFWC) and the bark (DFBC) at 500 °C using an auger driven reactor with a nitrogen sweep gas under mild vacuum. Five ozone treatment times, ranging from 5 min to 60 min, were investigated. The initial properties of each char were found to differ significantly from the other samples in terms of surface area, proximate composition, and elemental composition. DFWC did not show significant mass loss or temperature variation during ozone treatment; however, after 1 h of oxidation both DFBC and AC samples resulted in 20% and 30% mass loss, respectively, and reactor temperatures in excess of 60 °C. Analysis of the pore size distribution of each treatment shows that ozone treatment did not significantly affect small micropores after 30 min of treatment for any material, but did reduce the apparent surface area of mesopores. Increases in carboxylic groups were identified with ozone treatment and found to correlate strongly with changes in measured CEC. The formation of lactone was found to correlate positively with reactor temperature during oxidation. These results indicate that the properties of chars, including surface area, pore structure, and chemical composition, as well as reactor conditions strongly affect the ozone oxidation of chars.