Microscopy Characterization Research Articles

Waste coffee biochar and bi-oil composite modified rejuvenated asphalt: Preparation, characterization, and performance evaluation

In the realm of sustainable road construction, bio-oil has emerged as a promising and eco-friendly alternative for rejuvenating aged asphalt. Nevertheless, challenges arise due to poor stability, diminished performance at elevated temperatures, and limited anti-aging properties. This study introduces an innovative approach by blending biochar, obtained from the pyrolysis of waste coffee grounds, into bio-oil to create a composite modified regenerator. Initially, the study conducts a microscopic characterization of the biochar using X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDS). Subsequently, the rheological properties of this composite rejuvenated asphalt are evaluated across low, moderate, and high-temperature ranges using bending beam rheometer (BBR), linear amplitude sweep (LAS), and multiple stress creep and recovery (MSCR) tests. Departing from the traditional emphasis on initial property restoration, it further delves into performance alterations after re-aging of rejuvenated asphalt through temperature sweep (TS) and Fourier transform infrared spectroscopy (FTIR) tests, providing a comprehensive assessment of the anti-aging characteristics of rejuvenated asphalt. Additionally, gel permeation chromatography (GPC) is employed to quantitatively analyze the changes in asphalt molecular weight distribution. The microscopic characterization reveals the development of a rough and porous structure within the biochar, facilitating enhanced adhesion and interaction between the rejuvenator and the asphalt binder. Moreover, bio-oil rejuvenated asphalt exhibits excellent low-temperature crack resistance and moderate-temperature fatigue resistance. Following the incorporation of biochar, notable enhancements in high-temperature rutting resistance and anti-aging properties are observed, validating the efficacy of the biochar with bio-oil composite modified regenerator. To achieve optimal performance outcomes, a biochar content of 6 % (as a proportion of aged asphalt), corresponding to a 1:1 ratio of biochar to bio-oil, is recommended. Under this condition, the properties of the composite modified rejuvenated asphalt demonstrate comparability to those of the original asphalt. In summary, this research underscores the potential for integrating waste coffee biochar material into infrastructure development, thereby promoting circular economy principles and advancing more sustainable construction practices.

Microstructure and wear resistance of laser cladding AlCoCrFeNiSiB high-entropy alloy with high boron content

In this study, a wear-resistant coating of high boron content Al1.5CoCr2Fe1.5NiSi0.5B2 high-entropy alloy (HEA) was prepared on X65 pipeline steel by laser cladding. The coating underwent microhardness testing, wear performance testing, and analyses including scanning electron microscope (SEM), transmission electron microscope (TEM), and X-ray diffraction (XRD). The results revealed a dual-phase structure of body-centered cube (BCC) and face-entered cube (FCC) in the coating, with the presence of Fe1.1Cr0.9B0.9 phase distributed within the BCC. Utilizing high-resolution transmission electron microscopy (HRTEM) characterization, irregular atomic arrangement regions within the BCC structure were observed. Through the calculation of the α2 and ε parameters of the coating, the degree of lattice distortion in the BCC and FCC phases was quantitatively described. The results suggested that the addition of a substantial amount of boron could strengthen the lattice distortion effect, leading to improved hardness and wear resistance of the coating. The average microhardness of the coating was 912 HV, about 5 times higher than X65 substrate, improved by more than 10 % compared with other AlCoCrFeNi-based high-entropy alloys and B-containing high-entropy alloys. The wear rate was 4.78 × 10−6 mm/N·m, wear performance is nearly 10 times higher than other AlCoCrFeNi HEA without boron, 2 times higher than HEA with born. The wear mechanism of the coating was identified as abrasive and oxidative wear.

Gradient structured Al alloy with a synergistic improvement of strength-ductility obtained by friction stir processing

One Al 6061 with gradient microstructure is prepared by friction stir processing (FSP). Microscopic characterization indicates that the regulation of grain size gradient could be achieved by adjusting the process parameters of FSP. The mechanical property test indicates that one gradient Al 6061 combines an ultimate tensile strength of 266 MPa with a uniform elongation of 27 %, and the other comes 258 MPa with 29 %, which provides an excellent combination of strength and ductility. Moreover, the molecular dynamics (MD) method is employed to reconstruct and simulate the mechanical behavior of the gradient region and the dynamic evolution of the microstructure. When the stacking faults (SFs) with antisymbolic Burgers vector meet and detwinning occurs, grain refinement will induce localized strengthening. When the Shockley partials occur cross-slip, numerous sessile dislocations obstruct the dislocation motion more facilitate strain hardening. Meanwhile, a unique interaction mechanism between shear bands (SBs) and intergranular cracks in Al 6061 is discovered in plastic deformation. The coarse net-like SBs in the small-grain region are highly susceptible to catastrophic fracture of the material, and the large cracks formed within the severely band-like SBs in the large-grain region weaken the strength substantially. However, the formation of sessile dislocations in the gradient region effectively mitigates strain localization and inhibits the nucleation of large cracks. The results interpret the dynamic evolution process of gradient microstructure prepared by FSP and the mechanism of strengthening and toughening and provide process and theoretical references for the research and development of new engineering materials.

Effects of heat input on microstructure evolution and corrosion resistance of underwater laser cladding high-strength low-alloy steel coating

The effects of heat input on the microstructure evolution and corrosion resistance of the high-strength low-alloy (HSLA) steel coating obtained by wire-feed underwater laser cladding were studied. Optical digital microscope, scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), transmission electron microscope (TEM), electron back-scattered diffraction (EBSD), electrochemical tests, laser microscope and other characterization methods were used. As the heat input increased, the smoothness of the underwater cladding coating improved, with little changes in elemental distribution and phase composition. However, the content of acicular ferrite increased, while the amounts of lath bainite, lath martensite, and granular bainite decreased. As the heat input increased from 0.4 to 0.55 kJ/mm, the grain size increased from 25.3 to 55.9 μm, the proportion of low-angle grain boundaries rose from 61.3 % to 69.1 %, and the texture intensity of the (110) crystal plane increased from 16.22 to 23.83. Meanwhile, the dislocation density decreased from 4.9 × 1014 to 4.1 × 1014 m−2. These changes enhanced the corrosion resistance of underwater coating. As the heat input increased from 0.4 to 0.55 kJ/mm, the corrosion current density decreased from 2.13 × 10−5 to 3.35 × 10−6 A/cm2, and the corrosion potential increased from −0.823 to −0.529 V. Additionally, the depth-to-width ratio of the corrosion pits decreased from 0.255 to 0.053. This study laid the foundation for high-quality in-situ underwater repairs of ships and submarines made of high-strength steel.

Underlying mechanisms for the effect of Nb micro-alloying on the elemental distribution and precipitation behavior in the X70 weld metal

Niobium (Nb) is a widely recognized micro-alloying element due to its low cost and substantial impact on steel properties. While the effect of Nb in processed steels has been well investigated, studies on its elemental distribution and precipitation behavior in weld metal remain scarce. This study focuses on the weld metal of specially designed Nb-rich X70 pipeline steel by scanning transmission electron microscopy (STEM) and energy-dispersive X-ray spectroscopy (EDS) characterization, complemented with thermodynamic and kinetics modeling analysis. In the majority of the weld, Nb was essentially uniformly distributed. This suggests that Nb primarily exists in the solid solution form in the weld metal, which is also supported by precipitation kinetics modeling results. This is primarily due to the short thermal history associated with the welding process, which leads to insufficient time for the uniform precipitation of Nb. Two instances of Nb precipitates were observed at the weld centerline and reinforcement region. The low partition coefficient of Nb results in an elevated local concentration along the weld centerline. However, precipitation kinetics calculations suggest that this enhancement alone is not adequate to induce precipitate formation. The occurrence of MnS and the prior formation of Ti precipitates may provide heterogeneous nucleation sites for Nb, facilitating the nucleation of Nb precipitates in the weld centerline and reinforcement region.

Mechanisms of dissolution and crystallization of amorphous glibenclamide

Amorphous solid dispersions enhance the dissolution and oral bioavailability of poorly water-soluble drugs. However, the link between polymer properties and formulation performance has not been fully clarified yet. We studied the effect of hydroxypropyl cellulose (HPC) polymers molecular weight (Mw) on the storage stability, dissolution kinetics and supersaturation stability of spray-dried amorphous glibenclamide (GLB) formulations. The solid-state stability of amorphous GLB during storage was significantly enhanced by both the 40 kDa (HPC-SSL) and 84 kDa (HPC-L) polymers, regardless of Mw differences. In contrast, HPC-SSL maintained significantly higher aqueous drug concentrations during dissolution, compared to HPC-L (its higher Mw analogue). Dedicated dissolution experiments, in situ optical microscopy and solid-state characterization revealed that aqueous drug concentrations were determined by the interplay between crystallization inhibition, drug ionization, wetting and solubilization effects: (1) HPC prevents surface nucleation, hence inhibiting crystallization, (2) intestinal colloids (bile salts and phospholipids) increase supersaturated drug concentrations via wetting and solubilization effects and (3) pH and drug ionization severely impact the degree of supersaturation. The better performance of the lower Mw HPC-SSL was due to its superior inhibition of surface crystallization. These insights into the molecular mechanisms of dissolution and crystallization of amorphous solids provide foundation for rational formulation development.

Research on corrosion behavior and biocompatibility of NiTi alloy processed with combined dealloying and annealing treatment

This paper presents a novel method to prepare hydrophilic nanoporous functional surface with combined dealloying and annealing treatment to improve the corrosion resistance and biocompatibility of NiTi components. Surface modification mechanism is discussed with microscopic characterization of NiTi nanoporous structures. Hydrophilic and biocompatible performance is achieved through specifically tailoring the dimensions and chemical compositions of nanoporous layer. The corrosion resistance of NiTi samples is investigated in 0.9 wt% NaCl solution and evaluated with potentiodynamic polarization and electrochemical impedance spectroscopy tests. The results indicate that material corrosion resistance is significantly enhanced with TiO2 formation during dealloying treatment, while annealing promotes the oxidation and densification of dealloyed layer raising the energy barrier for ion transportation during corrosion. Furthermore, as the dealloying temperature increases, the surface defects of the sample decrease resulting in better corrosion resistance. The research can provide guidance for NiTi surface modification to enhance its biomedical applications.

High temperature environmental scanning electron microscopy characterization of transient phase formation during conversion of simulated nuclear waste feed to glass

In-situ High-Temperature Environmental Scanning Electron Microscopy (HT-ESEM) is used to characterize the transient phases formed during the melting of complex glass batch mixtures representing simulated nuclear waste feeds. The first phenomenon that occurs is the formation of oxyanionic salt melt, followed by the reaction of oxyanionic salts with refractory grains containing Si, Al, or Mg through surface reactions to form a molten alkali-alumino-boro-silicate phase. The onset temperatures of gas bubble formation and primary foaming are directly determined from the HT-ESEM measurements. The formation of sulfate lakes as well as the formation of high-temperature transient phases floating at the sample surface are also directly observed and identified. Convection currents are observed and their consequences on glass homogenization are discussed.

Advanced Electron Microscopy Characterisation of Aluminium-Oxygen Coordination in Catalyst Supports

Performance of alumina-supported catalyst systems are significantly affected by how the tetrahedral (Al-O4) and octahedral (Al-O6) coordination are mixed and blended with each other. Characterisation of aluminium-oxygen coordination is thus important to understand how catalysts interact with alumina at the microscopic level. Here we report the application of two advanced electron microscopy techniques on aluminium-oxygen coordination. The first technique is electron energy loss spectroscopy (EELS) that can reveal detailed electronic structure profile of aluminium valence band to analyse how aluminium is coordinated by oxygen. The second technique is pair distribution function (PDF) based on electron diffraction (ED), employed to measure aluminium-oxygen bond lengths associated with the coordination geometry.

A unique kind of distribution band of martensitic laths formed along {332}〈113〉 twin boundary in the Ti[sbnd]42Nb alloy subjected to instable deformation

Multi-scale electron microscopy characterization of the {332}<113 > β twins produced in the necking region near fracture surface of the deformed β-type Ti42Nb (wt%) alloy have been carried out. A unique kind of band-shaped zone with plenty of laths of two α″ martensitic subvariants distributed in about 90° crossing directions has been found to be formed in the {332}<113 > β deformation twin along the twin boundary. This finding clearly reveals that intense local stress concentration and its complex accommodation process associated with the β-to-α″ and α″-to-β structural transitions can occur specially in the twinned region of stress-induced α″ martensite phase along its boundary for the β Ti alloy subjected to instable deformation. It is also clearly indicated that the local stress accommodation due to the α”-to-β structural transition can be unsymmetrical with respect to the twin boundary.

Alkyne-rich patchy polymer colloids prepared by surfactant-free emulsion polymerization

While free radical polymerization methods are employed frequently to prepare sub-micron polymer particles, we hypothesized that surfactant-free emulsion polymerization (SFEP)1Surfactant-free emulsion polymerization1 methodology may prove beneficial for obtaining functional polymer particles by solution polymerization methods that preclude the need for conventional surfactants. To test the effectiveness of SFEP for the preparation of functional colloids, solution polymerization of several monomers, including propargyl acrylate (PA),2Propargyl acrylate.2 styrene (Sty)3Styrene.3 and tert-butyl acrylate (t-BA),4Tert-butyl acrylate.4 was performed over a range of monomer ratios and reaction scales. Electron microscopy and infrared spectroscopy were employed to evaluate the outcome of SFEP for particle size, shape, surface anisotropies, and chemical composition. Combining this characterization with optimized SFEP synthesis, we found that spherical polymer particles—homopolymers of PA as well as copolymers—were obtained in the 60–300 nm diameter size range. Successful inclusion of PA enabled the use of the particles in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc).5Copper-catalyzed azide-alkyne cycloaddition5 Moreover, electron microscopy characterization with backscattering revealed chemical and shape anisotropies on copolymer particles indicative of monomer phase-separation during particle formation. Overall, the SFEP methodology represents a straightforward, one-pot, bottom-up approach to yield a library of functional polymer particles, while avoiding undesirable aspects associated with conventional surfactants.

Effect of cellulose nanocrystals on the emulsion stability and rheological properties of microalgal Pickering emulsions

This study investigates the effect of cellulose nanocrystals (CNCs) to Pickering emulsions prepared with microalgal particles (Spirulina sp. (SPI), Chlorella sp. HS2 (CLO)). The microalgae particles show a weak interfacial localization and Pickering behavior on the O/W emulsion depending on the size (avg. drop size ∼5.39 μm with SPI and 22.15 μm with CLO), resulting in a different stabilization effect. When CNC is additionally mixed with the Pickering emulsions including large microalgae particles (CLO), CNC replaces microalgae particles and localizes at the interface, enhancing strong emulsion stabilization. For the Pickering emulsions including small microalgae (SPI), CNC localizes at the continuous phase, forming a network structure regardless of the concentration. This interfacial localization behavior of CNC against microalgae particles is reflected in the rheological behavior of the Pickering emulsion. Depending on the location of CNC, the emulsions exhibit the two-step yielding behavior, mainly attributed to the CNC network in the continuous phase. The complex role of particles in the emulsion system is more sensitively reflected in the large amplitude oscillatory shear (LAOS) region, characterized using the sequence of physical process (SPP) rheological analysis. The maximum elasticity (Emax) in SPP analysis, which indicates the recovery of the deformed structure, exhibits a significant difference, discriminating structural characteristics of CNC dispersion incorporated with microalgae particles. Emulsion with CLO-CNC has lower Emax than the SPI-CNC case because CNC particles disperse at the interface and the continuous phase. Then the distance between CNC particles is longer, resulting in a weak network structure throughout the emulsion. Due to a weak network of CNC, the emulsion is more vulnerable to coalescence compared to the SPI-CNC system. Therefore, this study suggests that CNC particles added to the Pickering emulsion with microalgae compete to localize at the interface and give coalescence suppression effects to the emulsion. Also, for the Pickering emulsion system composed of multi-particles, rheological analysis including SPP analysis successfully indicates structural characteristics and flow-induced stabilization of Pickering emulsions with multi-particles that microscopic characterization could not detect.

Photothermal Properties of Solid-Supported Gold Nanorods.

Gold nanoparticles possess unique photothermal properties and have gained considerable interest in biomedical research, particularly for photothermal therapy (PTT). This study focuses on evaluating the photothermal properties of gold nanorods (AuNRs) supported on glass substrates upon excitation with near-infrared (NIR) light. Two aspect ratios of AuNRs were electrostatically immobilized onto glass with controlled coverage. In situ X-ray diffraction (XRD) was performed to evaluate the photothermal behavior and morphological changes of the supported AuNRs during NIR laser irradiation. The XRD data sets were corroborated with scanning electron microscopy and Vis-NIR spectroscopy characterization. XRD revealed a linear temperature increase with laser power, aligning with theoretical predictions, and a slope dependent on the AuNR coverage, until the onset of morphology transformations around 120 °C. This study provides valuable insights into the photothermal properties of supported AuNRs, crucial for their application in PTT.

In-Situ EBSD investigation of how annealed twins produce excellent strength-ductility synergy in Al0.25FeCoNiV duplex high-entropy alloy

The development of high-entropy alloys (HEAs) has been historically constrained by trade-off between strength and ductility. In this study, the Al0.25FeCoNiV duplex HEA showed a yield strength of 625 ± 35.2 MPa and a fracture elongation of 48 ± 1.5 % after rolling and annealing. These values are 43 % and 60 % higher, respectively, than the as-cast specimens, demonstrating an excellent synergy between strength and ductility. Through in-situ electron backscatter diffraction (EBSD) tensile experiments and transmission electron microscopy characterization of the as-cast and annealed specimens, respectively, it is found that the superior mechanical properties of the annealed specimens are primarily attributable to the multilevel strengthening and strain-hardening coupling mechanism established by the synergistic action of phase boundaries (PBs), twin boundaries (TBs), and high-angle grain boundaries. This mechanism effectively suppresses strain localization and prevents premature fracture caused by local stress concentration at PBs. The strengthening mechanism of TBs on the mechanical properties of HEAs was investigated by examining the interaction mechanisms between annealed TBs and dislocations, as well as the coordinated plastic deformation mechanism of twins. This study provides novel insights into the development of innovative HEAs with enhanced properties and advances the understanding of the role of TBs in the strengthening mechanisms of materials.

Structure-activity relationship, adsorption, and fenton-like catalytic oxidation capacity of iron-oxide nano-confined materials

In this study, iron-oxide was loaded into polystyrene macroporous microspheres containing sulfonate groups to prepare an environmental purification material with adsorption and Fenton-like oxidizing abilities. Iron-oxide is prone to inactivation due to reunion in the process of preparation and application, and this modification aimed to mitigate this problem. Subsequently, based on the microscopic characterization results and the effect on the treatment of methylene blue (MB) simulated wastewater, the structure-activity relationship of two key (OH− concentrations in precipitation solution and iron ion compositions in the impregnation solution) factors with the adsorption and catalytic oxidation ability of the iron-oxide nano-confined materials were explored. The results indicated that the samples both exhibited adsorption and catalytic oxidation capabilities. The removal efficiency of MB simulated wastewater can reached 95.3% after adsorption for 9 h, reaching 99.98% after catalytic oxidation for 6 h. In addition, the removal efficiency of the MB simulated wastewater exceeded 95% after 6 cycles. The concentration of OH− in precipitation solution could affect the volume of iron crystals on the carrier which affected the pore size of the sample and the adsorption capacity. It also influenced whether iron ions could be stably loaded inside the carrier, determining the conducting homogeneous or heterogeneous Fenton-like reactions and the stability of the samples. The composition of iron ions in the impregnating solution regulated the volume of the crystals and adsorption sites, which influenced the adsorption ability of the samples. In addition, the presence of Fe2+ could promote the progress of Fenton-like reactions. The identification results of the ROSs showed that •OH was the main free radical. The quenching experiment results showed that the contribution rate of •OH toward MB degradation reached 99.81%. In addition, the possible degradation pathways of MB were analyzed.

Ni-Doped SFM Double-Perovskite Electrocatalyst for High-Performance Symmetrical Direct-Ammonia-Fed Solid Oxide Fuel Cells.

Ammonia has emerged as a promising fuel for solid oxide fuel cells (SOFCs) owing to its high energy density, high hydrogen content, and carbon-free nature. Herein, the electrocatalytic potential of a novel Ni-doped SFM double-perovskite (Sr1.9Fe0.4Ni0.1Mo0.5O6-δ) is studied, for the first time, as an alternative anode material for symmetrical direct-ammonia SOFCs. Scanning and transmission electron microscopy characterization has revealed the exsolution of Ni-Fe nanoparticles (NPs) from the parent Sr2Fe1.5Mo0.5O6 under anode conditions, and X-ray diffraction has identified the FeNi3 phase after exposure to ammonia at 800 °C. The active-exsolved NPs contribute to achieving a maximal ammonia conversion rate of 97.9% within the cell's operating temperatures (550-800 °C). Utilizing 3D-printed symmetrical cells with SFNM-GDC electrodes, the study demonstrates comparable polarization resistances and peak power densities of 430 and 416 mW cm-2 for H2 and NH3 fuels, respectively, with long-term stability and a negligible voltage loss of 0.48% per 100 h during ammonia-fed extended galvanostatic operation. Finally, the ammonia consumption mechanism is elucidated as a multistep process involving ammonia decomposition, followed by hydrogen oxidation. This study provides a promising avenue for improving the performance and stability of ammonia-based SOFCs for potential applications in clean energy conversion technologies.

Preparation of Self-healing Thermoplastic Polysiloxane-Polyurea/Polyether-Polyurea Elastomer Blends with a Co-continuous Microphase Structure and In-Depth Research on Their Synergistic Effects.

Polymer blending has been an important method to create materials with specific properties that have synergistic effects. However, there are few reports on the mechanism of synergistic effects. It is well known that it is quite difficult to obtain ideal blends composed of nonpolar organosilicon polymers and polar polymers. In this paper, thermoplastic polyurea elastomer blends with a co-continuous microphase structure consisting of polysiloxane-polyurea (PDMS-PUA), polyether amine-polyurea (PEA-PUA), and compatibilizer PDMS-PUA-grafted PEA-PUA (PDMS-PUA-g-PEA-PUA) were prepared for the first time. For the first time, introduction of polysiloxane does not sacrifice mechanical properties of thermoplastic polyurea elastomers. For example, the tensile strength of the elastomer blend with 30 wt % PDMS-PUA content reached 25.7 MPa, which is higher than those of PEA-PUA and PDMS-PUA. The blends also show typical outstanding characters such as exceptional heat and water resistance. The mechanism of the synergistic effect on mechanical properties is revealed based on in-depth studies on mutual interphase interaction. In situ variable temperature infrared spectroscopic analysis (VTIR) shows that compatibilization facilitates the construction of a denser hydrogen bonding network at the blend interface, which is thought to play a key role in the co-continuous microphase structure. Microscopic morphological characterization shows that PDMS-PUA and PEA-PUA phases are deformed and oriented together during the stretching process, thus jointly resisting external forces. Moreover, the blends show an exceptional self-healing ability due to their strong and reversible hydrogen bonding network.

Antimicrobial Peptide Octoprohibitin-Encapsulated Chitosan Nanoparticles Enhanced Antibacterial Activity against Acinetobacter baumannii

Background: This study focused on evaluating the physiochemical characteristics and antibacterial activity of Octoprohibitin-encapsulated CNPs (Octoprohibitin-CNPs) against Acinetobacter baumannii. Methods: Octoprohibitin was encapsulated into CNPs via ionotropic gelation with carboxymethyl chitosan (CMC) and low molecular weight chitosan (CS). Octoprohibitin-CNPs were dispersed in phosphate-buffered saline and the release kinetic profile was determined. Then Octoprohibitin-CNPs were examined using field-emission transmission electron microscopy and physicochemical characterization was performed. Antibacterial activity of Octoprohibitin-CNPs against A. baumannii was evaluated. Biofilm inhibition and eradication assays were performed using the crystal violet (CV) staining-based method for biofilm quantification. Results: The average diameter, zeta potential, encapsulation efficiency, and loading capacity of Octoprohibitin-CNPs were 244.5 ± 21.97 nm, +48.57 ± 0.38 mV, and 85.7% and 34.2%, respectively. TEM analysis imaging revealed that Octoprohibitin-CNPs are irregularly shaped, with fewer aggregates than CNPs. Octoprohibitin-CNPs exhibited a biphasic release pattern, characterized by an initial rapid phase followed by a sustained release over time, extending up to 93.68 ± 6.48% total release until 96 h. In vitro, Octoprohibitin-CNPs showed lower cytotoxicity compared to Octoprohibitin alone. Time-kill kinetic and bacterial viability reduction assays showed Octoprohibitin-CNPs exhibited slightly higher antibacterial activity against A. baumannii than Octoprohibitin. Conclusions: Octoprohibitin-CNP-treated A. baumannii exhibited higher levels of morphological deviation, increased membrane permeability, and the production of reactive oxygen species, as well as antibiofilm activity with greater biofilm inhibition and eradication than Octoprohibitin. These findings show that Octoprohibitin-CNPs perform better against A. baumannii compared to Octoprohibitin alone.

Quasi-static and dynamic stab behavior and damage mechanisms of the spiral/laminated structure of CFRP

Stab resistance depends on the material’s strength and stiffness. Puncture energy is absorbed mainly through fracture and friction in the damaged area. To reduce stress concentrations and diffuse impact energy, this paper proposes a spiral CFRP inspired by spiral grass. Comparison of the puncture resistance of spiral CFRP and laminated CFRP by quasi-static and dynamic puncture. After separating the puncture process into longitudinal piercing and transverse cutting, it was found that spiral CFRP had excellent cutting resistance, with a maximum cutting force 44% higher than laminated CFRP. However, the detachment of the central structure leads to weaker perforation resistance of spiral CFRP than laminated CFRP. Laminated CFRP was found to undergo internal delamination damage after perforation by microscopic characterization and finite element analysis. Spiral CFRP has a helical yarn path and the interface distribution parallel to the impact direction, resulting in a greater susceptibility to delamination damage and rapid spiral crack propagation. The damaged area of spiral CFRP is up to 416% larger than that of laminated CFRP. The structural instability also resulted in a higher penetration depth for spiral CFRP than for laminated CFRP. The composite structure provides better puncture resistance than a single structure. Due to the combined advantages of the passivation of spiral CFRP and the structural stability of laminated CFRP, Sprial/laminated CFRP has the highest puncture resistance, with a maximum puncture load of 1,467 N, and is not penetrated at a puncture energy of 24 J. The spiral structure incorporating crack-inducing and transverse damage resistance could offer a promising approach to developing stab-resistant materials.

Recycle of Fe/Ca-rich fly ash in preparation of modified porous ceramsite for selective and efficient phosphate recovery

Although wastewater management has systematically developed globally, the removal efficiency of phosphates still posed a serious challenge and attracted worldwide concerns. On the other side, the discharge of fly ash (FA) from sludge incineration also caused serious environmental problems. In this study, Fe/Ca-rich FA was recycled to synthesize a porous ceramsite (modified CFA) through a non-sintered method. It could be an efficient adsorbent for phosphate recovery in virtue of abundant adsorption sites, accompanied by its low-cost and environmental friendliness. The phosphate adsorption capacity was 26.31 mg-P·g-1 for modified CFA, and its average adsorption rate could reach 1.344 mg-P·(g·day)-1 in the first 2 days. While it could also efficiently immobilize phosphate for a quite long period in the dynamic system effluent. According to electron microscopic and spectroscopic characterizations, modified CFA was indicated to chemisorb and immobilize phosphates via multiple interface interactions. Phosphates were firstly H-bonded with the surface Fe/Ca-OH of modified CFA and then rapidly coordinate with active Fe sites through a ligand exchange mechanism. When the exposed Fe sites had been saturated-adsorbed, inner-sphere Ca-O-P coordination would be further formed. In summary, this study provides a promising FA-derived adsorbent and realizes the efficient P pollution management with low cost and minimal environmental risks, which would be a potential waste-to-wealth strategy for further applications.