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Ultralight architected materials enabled by advanced manufacturing processes have achieved density-normalized strength and stiffness properties that are inaccessible to bulk materials. However, the majority of this work has focused on static loading and elastic-wave propagation. Fundamental understanding of the mechanical behavior of architected materials under large-deformation dynamic conditions remains limited, due to the complexity of mechanical responses and shortcomings of characterization methods. Here, we present a microscale suspended-plate impact testing framework for three-dimensional micro-architected materials, where supersonic microparticles to velocities of up to 850 m/s are accelerated against a substrate-decoupled architected material to quantify its energy dissipation characteristics. Using ultra-high-speed imaging, we perform in situ quantification of the impact energetics on two types of architected materials as well as their constituent nonarchitected monolithic polymer, indicating a 47% or greater increase in mass-normalized energy dissipation under a given impact condition through use of architecture. Post-mortem characterization, supported by a series of quasi-static experiments and high-fidelity simulations, shed light on two coupled mechanisms of energy dissipation: material compaction and particle-induced fracture. Together, experiments and simulations indicate that architecture-specific resistance to compaction and fracture can explain a difference in dynamic impact response across architectures. We complement our experimental and numerical efforts with dimensional analysis which provides a predictive framework for kinetic-energy absorption as a function of material parameters and impact conditions. We envision that enhanced understanding of energy dissipation mechanisms in architected materials will serve to define design considerations toward the creation of lightweight impact-mitigating materials for protective applications.
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Impact experiments enable single particle analysis for many applications. However, the effect of the trajectory of a particle to an electrode on impact signals still requires further exploration. Here, we investigate the particle impact measurements versus motion using micromotors with controllable vertical motion. With biocatalytic cascade reactions, the micromotor system utilizes buoyancy as the driving force, thus enabling more regulated interactions with the electrode. With the aid of numerical simulations, the dynamic interactions between the electrode and micromotors are categorized into four representative patterns: approaching, departing, approaching-and-departing, and departing-and-reapproaching, which correspond well with the experimentally observed impact signals. This study offers a possibility of exploring the dynamic interactions between the electrode and particles, shedding light on the design of new electrochemical sensors.
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Microeletrodos , BiocatáliseRESUMO
Chemical composition, size and structure of the nanoparticle are required to describe nanoceria. Nanoparticles of similar size and Ce(III) content might exhibit different chemical behaviour due to their differences in structure. A simple and direct procedure based on affordable techniques for all the laboratories is presented in this paper. The combination of Raman and UV-vis spectroscopy and particle impact coulometry (PIC) allows the characterization of nanoceria of small size from 4 to 65 nm at a concentration from micromolar to nanomolar, a concentration range suitable for the analysis of lab-prepared or commercial nanoparticle suspensions, but too high for most analytical purposes aimed at nanoparticle monitoring. While the PIC limits of size detection are too high to observe small nanoparticles unless catalytic amplification is used, the method provides a simple means to study aggregation of nanoparticles in the media they are needed to be dispersed for each application. Raman spectroscopy provided information about structure of the nanoparticle, and UV-vis about their chemical behaviour against some common reducing and oxidizing agents. Graphical Abstract To characterize nanoceria it is necessary to provide information about the shape, size and structure of the nanoparticles as well as the chemical composition.
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In this article, high-speed photographic investigations of the dynamic crack initiation and propagation in several inorganic glasses by the impact of small spherical and conical projectiles are described. These were carried out at speeds of up to approximately 2×10(6) frames s(-1). The glasses were fused silica, 'Pyrex' (a borosilicate glass), soda lime and B(2)O(3). The projectiles were 0.8-2 mm diameter spheres of steel, glass, sapphire and tungsten carbide, and their velocities were up to 340 m s(-1). In fused silica and Pyrex, spherical projectiles' impact produced Hertzian cone cracks travelling at terminal crack velocities, whereas in soda-lime glass fast splinter cracks were generated. No crack bifurcation was observed, which has been explained by the nature of the stress intensity factor of the particle-impact-generated cracks, which leads to a stable crack growth. Crack bifurcation was, however, observed in thermally tempered glass; this bifurcation has been explained by the tensile residual stress and the associated unstable crack growth. A new explanation has been proposed for the decrease of the included angle of the Hertzian cone cracks with increasing impact velocity. B(2)O(3) glass showed dynamic compaction and plasticity owing to impact with steel spheres. Other observations, such as total contact time, crack lengths and response to oblique impacts, have also been explained.
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Discrete element method simulations are conducted to probe the various regimes of post-impact behavior of particles with solid surfaces. The impacting particles are described as spherical agglomerates consisting of smaller constituent (or primary) particles held together via surface adhesion. Under the influence of a wide range of impact velocities and particle surface energies, five distinct behavioral regimes-rebounding, vibration, fragmentation, pancaking, and shattering-are identified, and force transmission patterns are linked to post-impact behavior. In the rebounding regime, the coefficient of restitution decreases linearly as impact velocity increases and the particle agglomerate experiences compaction. In the fragmentation regime, rebound velocity generally decreases with increasing fragment size. The rebound velocity of fragments decreases with time except for the smallest fragments, which can increase in velocity due to collisions with other fragments of high velocity. Particle breakage in the pancaking regime does not follow common mechanistic models of breakage.
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In the first decade of high-velocity microparticle impact research, hardly any modification of the original experimental setup has been necessary. However, future avenues for the field require advancements of the experimental method to expand both the impact variables that can be quantitatively assessed and the materials and phenomena that can be studied. This work explores new design concepts for the launch pad (the assembly that launches microparticles upon laser ablation) that can address the root causes of many experimental challenges that may limit the technique in the future. Among the design changes contemplated, the substitution of a stiff glass launch layer for the standard elastomeric polymer layer offers a number of improvements. First, it facilitates a reduction of the gap between launch pad and target from hundreds to tens of micrometers and thus unlocks a reproducibility in targeting a specific impact location better than the diameter of the test particle itself (±1.75 µm for SiO2 particles 7.38 µm in diameter). Second, the inert glass surface enables experiments at higher temperatures than previously possible. Finally-as demonstrated by the launch of thin-film Au disks-a launch pad made of materials standard in microfabrication paves the way to facile microfabrication of advanced impactors.
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Terapia a Laser , Dióxido de Silício , Reprodutibilidade dos Testes , Temperatura , Temperatura AltaRESUMO
The quantitative analysis of human platelets is important for the diagnosis of various hematologic and cardiovascular diseases. In this article, we present a stochastic particle impact electrochemical (SPIE) approach for human platelets with fixation (F-HPs). Carboxylate-functionalized polystyrene particles (PSPs) are studied as well as a standard platform of SPIE-F-HPs. For SPIE-PSPs (or F-HPs), [Fe(CN)6]4- was used as the redox mediator, and electro-oxidation of [Fe(CN)6]4- to [Fe(CN)6]3- was conducted on a Pt ultramicroelectrode (UME) by applying a constant potential, where the corresponding oxidation current is mass-transfer-controlled. When PSPs (or F-HPs) are introduced into aqueous solution with [Fe(CN)6]4-, sudden current drops (SCDs) were observed, which resulted from the partial blockage of a Pt UME by collision of an individual PSP (or F-HP). For SPIE-PSPs (or F-HPs), we found that it is essential to enhance the migration of PSPs (F-HPs) toward a Pt UME by maximizing the steady state current associated with electro-oxidation of [Fe(CN)6]4-. This was accomplished by increasing its concentration to the solubility limit. We successfully measured the concentration of F-HPs dispersed in aqueous solution containing [Fe(CN)6]4- with a minimum detectable concentration of 0.1 fM, and the size distribution of F-HPs was also estimated from the obtained idrop distribution based on the SPIE analysis, where idrop stands for the magnitude of the current drop of each SCD. Lastly, we revealed that HPs without the fixation process (WF-HPs) are difficult to quantitatively analyze by SPIE because of their transient activation process, which results in changes from their spherical shape. The observed difficulty was also confirmed by finite element analysis, which shows that idrop can be significantly increased, as an elongated WF-HP is adsorbed on the edge of an UME.
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Plaquetas/química , Separação Celular/métodos , Técnicas Eletroquímicas/métodos , Técnicas Eletroquímicas/instrumentação , Ferrocianetos/química , Humanos , Microeletrodos , Oxirredução , Platina/química , Poliestirenos/química , Processos EstocásticosRESUMO
The inhibition of self-discharge in a redox-enhanced electrochemical capacitor (Redox-EC) is crucial for excellent energy retention. Heptyl viologen dibromide (HVBr2) was chosen as a strong candidate of a dual-redox species in Redox-EC due to its solid complexations during the charging process, at which HV2+ is electrochemically reduced to HV+⢠and form a solid complex, [HV+⢷Br-], on an anode while Br- is electro-oxidized to Br3- and renders [HV2+·2Br3-] on a cathode. The solid complexes could not transfer across the separator, resulting in significant diminution of the self-discharge. In this Article, we present detailed electrochemical studies of formation of [HV2+·2Br3-] and [HV+⢷Br-], their redox features, and galvanic exchange reactions between the two types of dual-redox ionic solids on a Pt ultra-microelectrode (UME) in neutral (0.33 M Na2SO4) and acidic (1 M H2SO4) solutions. Most importantly, through voltammetric and particle-impact electrochemical analyses, we found that the redox and galvanic exchange reactions of the two dual-redox ionic solid complexes involve H+ transfer, which is the key process to limit the overall kinetics of the electrochemical reactions. We also rationalize the proton-accompanied galvanic exchange reaction based on computational simulation.
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The impact mechanics of micrometre-scale metal particles with flat metal surfaces is investigated for high-velocity impacts ranging from 50 m s-1 to more than 1 km s-1, where impact causes predominantly plastic deformation. A material model that includes high strain rate and temperature effects on the yield stress, heat generation due to plasticity, material damage due to excessive plastic strain and heat transfer is used in the numerical analysis. The coefficient of restitution e is predicted by the classical work using elastic-plastic deformation analysis with quasi-static impact mechanics to be proportional to [Formula: see text] and [Formula: see text] for the low and moderate impact velocities that span the ranges of 0-10 and 10-100 m s-1, respectively. In the elastic-plastic and fully plastic deformation regimes the particle rebound is attributed to the elastic spring-back that initiates at the particle-substrate interface. At higher impact velocities (0.1-1 km s-1) e is shown to be proportional to approximately [Formula: see text]. In this deeply plastic deformation regime various deformation modes that depend on plastic flow of the material including the time lag between the rebound instances of the top and bottom points of particle and the lateral spreading of the particle are identified. In this deformation regime, the elastic spring-back initiates subsurface, in the substrate.