Characterization and Spectroscopic Applications of Metal Foams From New Lightweight Materials

Lightweight materials such as metallic foams possess good mechanical, chemical, and physical properties, which make them suitable for a wide range of functional and structural applications. Metal foams have recently gained substantial interest in both industry and academia due to their low cost, thermal conductivity, high working temperature, vibration damping, specific mechanical properties, energy absorption, and heat resistance. The use of metal foams on a large scale and successful applications depend on a detailed understanding of their characteristic properties. Metallic foams are characterized by the morphology of the porous cells (size and shape, open or closed, macro and micro), pore topology, relative density, properties of the pore wall, and the degree of anisotropy. This contribution focuses on x-ray diffraction, Fourier transform infrared (FT-IR), and Raman spectroscopic applications used for the characterization of metal foam, and also a brief of the most important applications, including a significant number of examples given.

Transport receptor occupancy in Nuclear Pore Complex mimics

Nuclear Pore Complexes (NPCs) regulate all molecular transport between the nucleus and the cytoplasm in eukaryotic cells. Intrinsically disordered Phe-Gly nucleoporins (FG Nups) line the central conduit of NPCs to impart a selective barrier where large proteins are excluded unless bound to a transport receptor (karyopherin; Kap). Here, we assess 'Kap-centric' NPC models, which postulate that Kaps participate in establishing the selective barrier. We combine biomimetic nanopores, formed by tethering Nsp1 to the inner wall of a solid-state nanopore, with coarse-grained modeling to show that yeast Kap95 exhibits two populations in Nsp1-coated pores: one population that is transported across the pore in milliseconds, and a second population that is stably assembled within the FG mesh of the pore. Ionic current measurements show a conductance decrease for increasing Kap concentrations and noise data indicate an increase in rigidity of the FG-mesh. Modeling reveals an accumulation of Kap95 near the pore wall, yielding a conductance decrease. We find that Kaps only mildly affect the conformation of the Nsp1 mesh and that, even at high concentrations, Kaps only bind at most 8% of the FG-motifs in the nanopore, indicating that Kap95 occupancy is limited by steric constraints rather than by depletion of available FG-motifs. Our data provide an alternative explanation of the origin of bimodal NPC binding of Kaps, where a stable population of Kaps binds avidly to the NPC periphery, while fast transport proceeds via a central FG-rich channel through lower affinity interactions between Kaps and the cohesive domains of Nsp1.

Integrating Pore Architectures to Evaluate Vascularization Efficacy in Silicate-based Bioceramic Scaffolds

Pore architecture in bioceramic scaffolds plays an important role in facilitating vascularization efficiency during bone repair or orbital reconstruction. Many investigations have explored this relationship but lack integrating pore architectural features in a scaffold, hindering optimization of architectural parameters (geometry, size, curvature) to improve vascularization and consequently clinical outcomes. To address this challenge, we have developed an integrating design strategy to fabricate different pore architectures (cube, gyroid, hexagon) with different pore dimensions (∼350, 500, 650 μm) in the silicate-based bioceramic scaffolds via digital light processing technique. The sintered scaffolds maintained high-fidelity pore architectures similar to the printing model. The hexagon- and gyroid-pore scaffolds exhibited the highest and lowest compressive strength (from 15 to 55 MPa), respectively, but the cube-pore scaffolds showed appreciable elastic modulus. Moreover, the gyroid pore architecture contributed on a faster ion dissolution and mass decay in vitro. It is interesting that both μCT and histological analyses indicate vascularization efficiency was challenged even in the 650-μm pore region of hexagon-pore scaffolds within 2 weeks in rabbit models, but the gyroid pore constructs indicated appreciable blood vessel networks even in the 350-μm pore region at 2 weeks and high-density blood vessels were uniformly invaded in the 500- and 650-μm pore at 4 weeks. Angiogenesis was facilitated in the cube-pore scaffolds in comparison with the hexagon-pore ones within 4 weeks. These studies demonstrate that the continuous pore wall curvature feature in gyroid pore architecture is an important implication for biodegradation, vascular cell migration and vessel ingrowth in porous bioceramic scaffolds.

Characteristics of Viscoelastic-Surfactant-Induced Wettability Alteration in Porous Media

Wettability alteration is one of the most important mechanisms of surfactant flooding. In this work, the combined Amott/USBM (United States Bureau of Mines) method was applied to study the average wettability alteration of initially neutral cores after viscoelastic-surfactant (VES) filtration. The effects of static aging, dynamic aging, VES concentration, filtration flow rate, and pore radius on the alteration of a core’s average wettability were studied. The wettability-alteration trends measured by Amott and USBM were consistent, demonstrating that the overall hydrophilicity of the core was enhanced after VES filtration. The wettability alterations of the core brought about by dynamic aging were more significant than by static aging. The viscoelastic properties of the VES played an important role in altering the wettability. In addition, the ability of the VES to affect the core’s wettability was significantly enhanced when the VES concentration was increased, which was beneficial in increasing VES adsorption on the pore-wall surface, thus altering the overall wettability of the core. Increasing filtration flow rates can destroy those high-viscosity VES aggregates via the higher shear rate. A higher retention of VES makes the core more hydrophilic. The difference in the wettability of cores with different pore radius after VES filtration was not significant. The alteration of average wettability caused by VES in porous media provides a new vision for studying the EOR mechanism of VES.

Olefin Metathesis in Confinement: Towards Covalent Organic Framework Scaffolds for Increased Macrocyclization Selectivity

Covalent organic frameworks (COFs) offer vast structural and chemical diversity enabling a wide and growing range of applications. While COFs are well-established as homogeneous catalysts, so far, their high and ordered porosity has scarcely been utilized to its full potential when it comes to spatially confined reactions in COF pores to alter the outcome of reactions. Here, we present a highly porous and crystalline, large-pore COF as catalytic support in diene ring-closing metathesis reactions, leading to increased macrocylization selectivity. COF pore-wall modification by immobilization of a Grubbs-Hoveyda-type catalyst via a mild silylation reaction provides a molecularly precise heterogeneous metathesis catalyst. An increased macro(mono)cyclization (MMC) selectivity over oligomerization (O) for the heterogeneous COF-catalyst (MMC:O = 1.30) of up to 44% compared to the homogeneous catalyst (MMC:O = 0.90) was observed along with a substrate-size dependency in selectivity, pointing to diffusion limitations induced by the pore confinement.

Revisiting the carbon mesopore contribution towards improved performance of ionic liquid–based EDLCs at sub-zero temperatures

The important role of mesopores has been investigated in electric double-layer capacitors (EDLCs) operating from 24 °C down to − 40 °C by using two in-house synthesized carbons with hierarchical porosity. These carbons were prepared from colloidal nanoparticles of SiO2 as the template and d-glucose as the carbon source. A decrease in the average diameter of the nanoparticles from 12 to 8 nm results in increased surface area and offers a perfect match between ions of binary mixture of imidazolium-based fluorinated ionic liquids and the pores of carbon. Short-range graphene layers produced with 8-nm silica nanoparticles lead to the creation of transport channels which better accommodate ions. We explain these findings per coulombic interactions among the ions and between the pore wall and the ionic species under confinement and electrochemical polarization conditions. Further, it is shown that a microporous carbon (another in-house produced rice-husk carbon SBET = 1800 m2∙g−1) performs better than hierarchical carbons at room temperature; however, thanks to the large fraction of mesopores, the latter exhibit far higher capacitance down to − 40 °C. While the ordering of ions in confinement is more critical at room temperature and dictated by the micropores, low temperature performance of supercapacitors is determined by the mesopores that provide channels for facile ion movement and keep the bulk ionic liquid–like properties. Graphical abstract

Study of internal porous structure formation of the powder metallurgically prepared aluminium foam

The internal pore wall structure formation and density play an important role in improving the mechanical and thermal properties of the closed-cell aluminium foams. The present research work aims to investigate the internal structure formation of the aluminium foam prepared by powder metallurgy and the uniformity of the distribution of the pores when the minimum amount of TiH2 is added. The foamable precursor of two different aluminium alloys (Al-1050 and A5083) is produced with a TiH2 gaseous agent of 0.05 wt.%. The parameters analysed include the density, pore wall formations, pore, and metal density distribution inside the structure with the help of X-ray tomography. Furthermore, the image-processing technique has been adopted to produce the 3D surrogate model of the foam for visual inspection and analysis. The obtained results show the importance of the amount of TiH2 addition and of the foaming furnace temperature in deciding the internal porous structure formation. Further, the pore morphology of lower porosity foams (in the range of 30-40 % porosity) of the two alloys produced at 690 °C furnace temperature is investigated with the help of developed surrogate models. The presence of micropores and uniformity of the distribution of pores found brings the idea of choosing the optimized structure of foam for thermal energy storage systems associated with PCM.