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The current work predicted the permeance of CO[sub.2] across a ZIF-L@PDMS/PES composite membrane using two different models. The membrane was fabricated by dipping a PES hollow fiber membrane in a coating solution made using PDMS that contained ZIF-L. First, flat sheet ZIF-L@PDMS membranes were fabricated to verify the role of ZIF-L on the gas separation performance of the membrane. Based on the data, the presence of ZIF-L in the PDMS matrix allowed enhancement of both permeability and selectivity of CO[sub.2], where the maximum value was obtained at 1 wt% of ZIF-L. The performance of ZIF-L@PDMS layer, as a function of ZIF-L loading, was well-predicted by the Cussler model. Such information was then used to model the CO[sub.2] permeance across ZIF-L@PDMS/PES composite membrane via the correction factor, which was introduced in the resistance in series model. This work discovered that the model must consider the penetration depth and the inorganic loading (in the case of ZIF-L@PDMS/PES). The error between the predicted CO[sub.2] permeance and the experimental results was found to be minimal.

Melt-spun PA6/TiO[sub.2] fibers with TiO[sub.2] modified by silane coupling agents KH550 and KH570 at 0, 1.6, and 4 wt% provide a practical testbed to address three fiber-centric gaps: transferable interphase quantification, interphase-resolved indications of compatibility, and a reproducible kinetics–structure–property link. This work proposes, for the first time at fiber scale, a four-phase partition into crystal (c), crystal-adjacent rigid amorphous fraction (RAF-c), interfacial rigid amorphous fraction (RAF-i), and mobile amorphous fraction (MAF), and extracts an interfacial triad consisting of the specific interfacial area (S[sub.v]), polymer-only RAF-i fraction expressed per composite volume (Γ[sub.i]), and interphase thickness (t[sub.i]) from SAXS invariants to establish a quantitative interphase-structure–property framework. A documented SAXS/DSC/WAXS workflow partitions the polymer into the above four components on a polymer-only basis. Upon filling, Γ[sub.i] increases while RAF-c decreases, leaving the total RAF approximately conserved. Under identical cooling, DSC shows the crystallization peak temperature is higher by 1.6–4.3 °C and has longer half-times, indicating enhanced heterogeneous nucleation together with growth are increasingly limited by interphase confinement. At 4 wt% loading, KH570-modified fibers versus KH550-modified fibers exhibit higher α-phase orientation (Hermans factor f(α): 0.697 vs. 0.414) but an ~89.4% lower α/γ ratio. At the macroscale, compared to pure (neat) PA6, 4 wt% KH550- and KH570-modified fibers show tenacity enhancements of ~9.5% and ~33.3%, with elongation decreased by ~31–68%. These trends reflect orientation-driven stiffening accompanied by a reduction in the mobile amorphous fraction and stronger interphase constraints on chain mobility. Knitted fabrics achieve a UV protection factor (UPF) of at least 50, whereas pure PA6 fabrics show only ~5.0, corresponding to ≥16-fold improvement. Taken together, the SAXS-derived descriptors (S[sub.v], Γ[sub.i], t[sub.i]) provide transferable interphase quantification and, together with WAXS and DSC, yield a reproducible link from interfacial geometry to kinetics, structure, and properties, revealing two limiting regimes—orientation-dominated and phase-fraction-dominated.

Microbial adhesion on dental restorative materials may jeopardize the restorative treatment long-term outcome. The goal of this in vitro study was to assess Candida albicans capability to adhere and form a biofilm on the surface of heat-cured dental composites having different formulations but subjected to identical surface treatments and polymerization protocols. Three commercially available composites were evaluated: GrandioSO (GR), Venus Diamond (VD) and Enamel Plus HRi Biofunction (BF). Cylindrical specimens were prepared for quantitative determination of C. albicans S5 planktonic CFU count, sessile cells CFU count and biomass optical density (OD[sub.570 nm]). Qualitative Concanavalin-A assays (for extracellular polymeric substances of a biofilm matrix) and Scanning Electron Microscope (SEM) analyses (for the morphology of sessile colonies) were also performed. Focusing on planktonic CFU count, a slight but not significant reduction was observed with VD as compared to GR. Regarding sessile cells CFU count and biomass OD[sub.570 nm], a significant increase was observed for VD compared to GR and BF. Concanavalin-A assays and SEM analyses confirmed the quantitative results. Different formulations of commercially available resin composites may differently interact with C. albicans. The present results showed a relatively more pronounced antiadhesive effect for BF and GR, with a reduction in sessile cells CFU count and biomass quantification.

Bioorthogonal chemistry capable of operating in live animals is needed to investigate biological processes such as cell death and immunity. Recent studies have identified a gasdermin family of pore-forming proteins that executes inflammasome-dependent and -independent pyroptosis 1 – 5 . Pyroptosis is proinflammatory, but its effect on antitumour immunity is unknown. Here we establish a bioorthogonal chemical system, in which a cancer-imaging probe phenylalanine trifluoroborate (Phe-BF 3 ) that can enter cells desilylates and ‘cleaves’ a designed linker that contains a silyl ether. This system enabled the controlled release of a drug from an antibody–drug conjugate in mice. When combined with nanoparticle-mediated delivery, desilylation catalysed by Phe-BF 3 could release a client protein—including an active gasdermin—from a nanoparticle conjugate, selectively into tumour cells in mice. We applied this bioorthogonal system to gasdermin, which revealed that pyroptosis of less than 15% of tumour cells was sufficient to clear the entire 4T1 mammary tumour graft. The tumour regression was absent in immune-deficient mice or upon T cell depletion, and was correlated with augmented antitumour immune responses. The injection of a reduced, ineffective dose of nanoparticle-conjugated gasdermin along with Phe-BF 3 sensitized 4T1 tumours to anti-PD1 therapy. Our bioorthogonal system based on Phe-BF 3 desilylation is therefore a powerful tool for chemical biology; our application of this system suggests that pyroptosis-induced inflammation triggers robust antitumour immunity and can synergize with checkpoint blockade. In mouse models of cancer, a biorthogonal chemical system based on desilylation catalysed by phenylalanine trifluoroborate enables the controlled release of gasdermin to induce pyroptosis selectively in tumour cells

Hybrid silane-based coatings were developed via the sol–gel process using two precursors, vinyltrimethoxysilane (VTMS) and tetraethoxysilane (TEOS), and subsequently deposited onto three titanium-based substrates: commercially pure titanium Grade 2, Ti6Al4V, and Ti13Nb13Zr. Comprehensive physicochemical characterization was performed, including microstructural (optical and SEM), topographical (3D roughness), spectroscopic (FTIR), and electrochemical (potentiodynamic) analyses. The coatings were continuous, transparent, smooth, and exhibited high gloss with no visible cracks or surface defects. Surface roughness (Sa ≈ 0.3 μm) was consistent across all samples and remained unaffected by both the VTMS to TEOS ratio and the substrate type. Coating thickness ranged from 8 to 15 μm, as confirmed by both digital microscopy and thickness gauge measurements. All coatings demonstrated strong adhesion to the substrates. FTIR analysis confirmed the presence of key functional groups, such as CH[sub.2], C=C, C–H, Si–O–Si, Si–OH, Si–O–Ti, CH=CH[sub.2], and O–Si–O, regardless of the substrate type. Electrochemical tests in Ringer’s solution showed excellent corrosion resistance, particularly for coatings with a VTMS to TEOS ratio of 1:1. Post-corrosion imaging confirmed the integrity of the coatings and their effectiveness as protective barriers in simulated physiological environments. These findings support the potential of VTMS/TEOS sol–gel coating as a surface modification strategy for biomedical titanium implants.

Objective: The objective of this study was to evaluate the resin-ceramic adhesion of a long-carbon-chain silane (LCSI)-containing resin cement. Methods: Polished lithium disilicate ceramic discs were etched with hydrofluoric acid and randomly assigned into four groups; (PSAP), cemented using a silane-free resin cement with no prior priming; (PSAP-S), primed using a silane-containing primer before cementation using a silane-free resin cement; (PSAU), cemented using a LCSI-containing resin cement with no prior priming; (PSAU-S), primed as for the group (PSAP-S) and cemented using a LCSI-containing resin cement. The cemented blocks were sectioned into microbeams. The resin-ceramic microtensile bond strength (μTBS) was measured at 1 week and after thermocycling. The failure modes of the tested microbeams were evaluated. Results: The μTBS of the LCSI-containing and silane-free resin cements, either with or without a prior priming step, did not significantly differ. The adhesion of the LCSI-containing resin cement to lithium disilicate ceramic, either with or without a prior priming step, did not significantly deteriorate after artificial aging. Conclusions: The long-carbon-chain silane (LCSI) monomer incorporated in the resin cement eliminated the need for a silane priming step of a hydrofluoric acid-etched lithium disilicate ceramic.

Stimuli-responsive Pickering emulsions are recently being progressively utilized as advanced catalyzed systems for green and sustainable chemical conversion. Hierarchically porous metal-organic frameworks (H-MOFs) are regarded as promising candidates for the fabrication of Pickering emulsions because of the features of tunable porosity, high specific surface area and structure diversity. However, CO[sub.2]-switchable Pickering emulsions formed by hierarchically porous zirconium-based MOFs have never been seen. In this work, a novel kind of the amine-functionalized hierarchically porous UiO-66-(OH)[sub.2] (H-UiO-66-(OH)[sub.2]) has been developed using a post-synthetic modification of H-UiO-66-(OH)[sub.2] by (3-aminopropyl)trimethoxysilane (APTMS), 3-(2-aminoethylamino)propyltrimethoxysilane (AEAPTMS) and 3-[2-(2-aminoethylamino)ethylamino]propyl-trimethoxysilane (AEAEAPTMS), and employed as emulsifiers for the construction of Pickering emulsions. It was found that the functionalized H-UiO-66-(OH)[sub.2] could stabilize a mixture of toluene and water to give an emulsion even at 0.25 wt % content. Interestingly, the formed Pickering emulsions could be reversibly transformed between demulsification and re-emulsification with alternate addition or removal of CO[sub.2]. Spectral investigation indicated that the mechanism of the switching is attributed to the reaction of CO[sub.2] with amino silane on the MOF and the generation of hydrophilic salts, leading to a reduction in MOF wettability. Based on this strategy, a highly efficient and controlled Knoevenagel condensation reaction has been gained by using the emulsion as a mini-reactor and the emulsifier as a catalyst, and the coupling of catalysis reaction, product isolation and MOF recyclability has become accessible for a sustainable chemical process.

The initial focus of this study was placed on the conversion of waste into valuable substances. Waste cement was systematically processed to extract silica powder, which was subsequently functionalized with γ-aminopropyl-trimethoxy-silane (KH550) via covalent grafting. The surface-modified silica particles demonstrated optimized amphiphilicity for interfacial stabilization, as confirmed by contact angle measurements. When employed in styrene/water Pickering emulsions, these modified silica particles exhibited exceptional stabilization efficiency, enabling the synthesis of core–shell polystyrene/silica composite microspheres visualized by SEM. It was demonstrated by the results that the Pickering emulsions could be stabilized by SiO[sub.2] when the appropriate polarity and concentration were achieved. XRD revealed successful silica integration without crystalline phase alteration. Thermogravimetric analysis demonstrated significantly enhanced thermal stability (50.6% residual mass at 800 °C), indicating substantial flame retardancy potential. This waste-to-functional-material strategy not only addresses environmental concerns but also provides an economically viable pathway for advanced polymer composites.

Mild steel continues to be the most extensively used construction material in several industries and constructions. However, corrosion of mild steel in aggressive environments is a major concern. Under the tremendously increasing demand for improving the coatings strategies because of the environmental concerns due to some of the traditional coatings, silane pre-treatments have been emerging as one of the effective solutions, among other strategies. Different approaches, such as adding particles of metal oxide (such as SiO2, ZrO2, Al2O3, TiO2 and CeO2), incorporating plant extracts and impregnating 2D materials into the coatings, have been employed for durable corrosion resistance, including for mitigating enhanced corrosion due to the presence of bacteria. This review discusses the critical mechanistic features of silane coatings such as the role of hydrolysis and condensation in the bonding of silanes with metal surfaces. The factors that influence the performance of the silane coatings for corrosion resistance of mild steel are discussed. In particular, this review provides insight into silane coatings for mitigating microbiologically influenced corrosion (MIC) of mild steel.

In this study, 3-trimethoxy-silylpropane-1-thiol (MPTMS) was used as a surface modifier for Al[sub.2]O[sub.3] powder to systematically analyze the effects of MPTMS concentration on the rheological properties, photocuring characteristics, and 3D printing performance of photocurable composite slurries. MPTMS concentration significantly influenced the rheological behavior of the slurry. Slurries containing 2 wt.% and 5 wt.% MPTMS exhibited a wide linear viscoelastic range (LVR). However, at concentrations of 10 wt.% and 20 wt.%, the LVR range narrowed, which led to reduced dispersion stability. In dispersion stability tests, the slurry with 2 wt.% MPTMS showed the most stable dispersion, while the 5 wt.% MPTMS concentration exhibited the highest photocuring rate. In 3D printing experiments, the 5 wt.% MPTMS concentration resulted in the most stable printed structures, whereas printing failures occurred with the 2 wt.% concentration. At 10 wt.% and 20 wt.%, internal cracking was observed, leading to structural defects. In conclusion, MPTMS forms silane bonds on the Al[sub.2]O[sub.3] surface, significantly impacting the stability, rheological properties, and printing quality of Al[sub.2]O[sub.3]-acrylate composite slurries. An MPTMS concentration of 5 wt.% was found to be optimal, contributing to the formation of stable and robust structures.