Capillary Condensation Research Articles

D-BJH: The Intrinsic Model for Characterizing the Pore Size Distribution of Porous Materials.

A novel approach, the differential Barrett-Joyner-Halenda model (D-BJH), is proposed to address the limitations of the traditional BJH model in determining the pore size distribution (PSD). This method integrates multilayer adsorption and capillary condensation processes using advanced numerical techniques, notably, a Galerkin-based framework for solving the differential BJH equations. The D-BJH model offers a precise analytical framework, establishing itself as a benchmark in adsorption theory. It enables accurate PSD calculations and provides robust theoretical support for interpreting adsorption isotherms. Additionally, a simplified D-BJH method allows for direct point-by-point PSD calculation, reducing computational complexity and eliminating cumulative errors inherent in traditional methods like BJH, DH, CI, and VBS. The D-BJH model demonstrates that PSD is directly related to the differential function of the isotherm and pore size concerning relative pressure. Comparative analyses with BJH, DH, and NLDFT models show that D-BJH effectively explains fundamental adsorption mechanisms, such as the "spurious peak" observed in desorption branches. This work expands the applicability of the BJH model, proving that both the D-BJH model and its simplified method are accurate and comprehensive for characterizing the pore structures of microporous and mesoporous materials.

NaCl aerosol filtration over filter media with intrafiber porosity: can filtrate capacity be increased by wicking into this pore volume?

This paper investigates a novel fiber-based filter media wherein a NaCl filtrate is collected and reservoired not only onto the surfaces of the fibers and within their inter-fiber voidage but also within the internal porosity of high pore volume nanoporous fibers or vapor grown carbon nanofibers (VGCF) floc used to fabricate the media. This transport process is shown to occur through a NaCl dissolution into the water-filled nanopores of the fiber and a subsequent intra-fiber wicking phenomenon. The study further elucidates two distinct NaCl accommodation mechanisms which are uniquely available to filter media containing nanoporous intrafiber porosity: (1) wicking and capillary condensation of liquid NaCl aerosols directly into the intrafiber pores at high RH, and (2) dissolution of otherwise solid NaCl aerosols deposited onto fiber surfaces (at low RH) into the interior nanopores of the fiber because these pores (when hydrophilic) are saturated with water (even at low RH). To investigate these two mechanistic regimes, various media were fabricated possessing multiscale porosity in the form of: (i) embedded flocs of VGCFs (4.108 cm3gm-1pore volume), (ii) hydrophilic and high pore volume activated carbon fibers (ACFs, 0.950 cm3gm-1) and (iii) solid graphite fibers. These media were then comparatively evaluated toward NaCl aerosol filtration at different relative humidities. Pressure drop measurements versus filtrate accumulation and SEM-EDAX VGCF demonstrated the location and transport of NaCl into the intrafiber voidage. Media containing both VGCF floc and ACF accumulated 1200% more NaCl at low RH (and a specified pressure drop) than similar media prepared from non-porous graphite fibers, with an additional 315% increase from low to high RH. A Gibbs free energy driving force model is provided to illustrate the driving forces favoring water condensation into the nanopores and solid NaCl aerosol dissolution into the water phase. Filtration efficiency and quality factor assessments for the various media are also systematically evaluated to demonstrate the observed mechanistics.

Comparative study of two mesoporous magnetic and MCM-41 supported Cu complex: High-performance heterogeneous catalysts for aqueous synthesis of tetrazole

The effects of the carrier were studied in the synthesis of tetrazole. Copper catalysts supported on CoFe2O4 and MCM-41 with serine ligands were prepared. Two mesoporous catalysts, CoFe2O4/Ser/Cu and MCM-41/Ser/Cu, (denote Serine with (Ser)) were synthesized and compared the activity of these catalysts in converting nitrile to tetrazole. The prepared material was characterized using powder X-ray diffraction (XRD),field emission scanning electron microscopy (SEM), energy-dispersive X-ray spectrometer (EDS), elemental mapping, vibrating-sample magnetometer (VSM), and nitrogen adsorption–desorption isotherm. The relation between the textural properties of the catalysts and the catalytic performance was investigated. The X-ray diffraction patterns showed the spinel ferrite type for CoFe2O4/Ser/Cu and amorphous SiO2 for MCM-41/Ser/Cu. The distinctive diffraction peaks in the diffraction curves of CoFe2O4/Ser/Cu, and MCM-41/Ser/Cu were identical to those of CoFe2O4, and MCM-41, confirming the preservation of these phases of supports throughout the functionalization processes and formation of -Ser/Cu moiety on the crystalline CoFe2O4 structure and non-crystalline silica structure. FE-SEM images showed the particles in CoFe2O4/Ser/Cu had an average diameter of 20–50 nm and in MCM-41/Ser/Cu had an average diameter of 50–250 nm. The images showed the uniformity and well-ordering of the particles. The slight aggregation in CoFe2O4/Ser/Cu particles implied that their clustering may be the result of modest attraction forces between them. MCM-41/Ser/Cu sample exhibited a type IV isotherm with an H1-type hysteresis loop and diagrams of the CoFe2O4/Ser/Cu showed a type IV isotherm (type H2 hysteresis loop). The MCM-41/Ser/Cu and CoFe2O4/Ser/Cu showed a mesoporous structure and capillary condensation occurred in the nearly cylindrical and ink bottle channels with non-uniform size or shape. The CoFe2O4/Ser/Cu showed surface area by BET and t-plot of 71.17 m2/g and 64.92 m2/g respectively, mean pore size of 14.06 nm, and pore volume of 0.250 cm3/g. The MCM-41/Ser/Cu showed surface area by BET and t-plot of 639.2 m2/g and 484.6 m2/g respectively, with a mean pore size of 5.44 nm, and pore volume of 0.869 cm3/g. The BJH pore size distribution was between 1 and 10 nm for the MCM-41/Ser/Cu and 1–20 nm for the CoFe2O4/Ser/Cu. Two catalysts were used for the synthesis of tetrazole. The CoFe2O4/Ser/Cu shows better activity in the synthesis of 5–substituted 1H-tetrazoles than the MCM-41/Ser/Cu sample despite its lowest surface area (71.17 m2/g). There is no reduction in the conversion of nitrile to tetrazole after the 6 cycles for CoFe2O4/Ser/Cu and after the 4 cycles for MCM-41/Ser/Cu.

Comparative predictive analysis using ANN and RCA for experimental investigation on branched and conventional micro heat pipe

The demand for compact, high-performance electronic devices rises, making thermal management in limited space crucial. This study presents a novel branched micro heat pipe (MHP) to solve this pressing problem. This novel method improves thermal performance for small-scale electronic cooling applications, surpassing conventional cooling methods. Innovative design has branched condenser of 12.7 mm evaporator, 24.6 mm adiabatic section and 12.7 mm condenser, each, compared to conventional MHP of identical size. Investigation encompasses a study of various parameters including working fluids, wettability characteristics, fill ratio, heat input, and cross-sectional geometries. The significant improvement in thermal performance by applying a hydrophobic surface treatment to the condenser section, increasing capillary force and condensate transport. Ammonia and de-ionized water excel thermal performance at lower and higher applied heat input (Qh), respectively. At higher Qh (>2 W), ammonia and toluene in the conventional MHP experience faster drying compared to the branched MHP, especially for lower fill ratio (0.6 FR). The branched MHP outperforms the conventional MHP, showing improved fluid circulation and performance, for fill ratios ranging from 0.65 to 0.4 and effectively transporting maximum heat flux in range of 10–14.4 W/cm2 with square mono-grooved MHP exhibits inferior performance compared to the trapezoidal and triangular mono-grooved. To provide a framework for future studies, we establish an artificial neural network (ANN) and statistical prediction model of thermal performance using the non-dimensional Kutateladze number (Ku), showcasing a robust correlation with experimental results and demonstrating only a minor deviation of ± 3 %.

Organosilica with tunable pore structure and antibacterial activity for intelligent humidity control

The spontaneous sorption and release of moisture by sorbents is proposed to be an energy-saving strategy for air humidity control. However, rational design of sorbents with humidity control ability and wide applicability still faces challenges. This study demonstrates quaternary ammonium-functionalized organosilica capable of controlling humidity intelligently and tuning humidity range as required. The prepared organosilica exhibited step-shaped water sorption isotherm due to its highly ordered pore structure, which was capable of precisely maintaining humidity within a narrow range. Importantly, the step position could be broadly tuned by easily changing the pore size during synthesis. Series organosilica with different pore sizes could realize humidity maintenance in 20%-40%, 40%-60% and 55%-80%, respectively, making it suitable for diverse humidity control applications. Grand Canonical Monte Carlo simulations elucidated the underlying mechanism of different water sorption behaviors in different pore structures. Quaternary ammonium groups act as the initial nucleation sites for water vapor, followed by distinct water condensation mechanisms in micropores (pore filling) and mesopores (capillary condensation), respectively. Moreover, organosilica exhibits efficient antibacterial activity and self-cleaning capability due to the function of quaternary ammonium groups. The organosilica with tunable pore structure and antibacterial activity provides a new model for intelligent and low-energy humidity control.

Small-Angle Scattering Indicates Equilibrium Instead of Metastable Capillary Condensation in SBA-15 Mesoporous Silica.

Questions about the origin of the adsorption/desorption hysteresis in mesoporous materials are as old as sorption experiments themselves. The historical conception that underlines most existing methods to extract pore size distributions from sorption data assumes that adsorption is a metastable process and that desorption takes place at thermodynamic equilibrium. In this work, we measure nitrogen and argon sorption on a series of 14 SBA-15 ordered mesoporous silicas and use small-angle X-ray scattering to independently determine their pore sizes. We find that capillary condensation systematically occurs close to thermodynamic equilibrium according to a Derjaguin-Broekhoff-de Boer calculation. Our analysis suggests that many earlier works have significantly underestimated the actual pore size in SBA-15 materials. It also highlights the critical role of the reference isotherm used to calibrate the fluid-solid interaction in the models.

The effect of traditional processing craft on the hygroscopicity of palm leaf manuscripts

Palm leaf manuscripts, which are crucial carriers of historical, religious, scientific, and artistic information in East and Southeast Asia, specifically encapsulate significant aspects of Buddhist culture and thus require comprehensive research and preservation efforts. The base material of palm leaf manuscripts is processed palm leaves, which are hygroscopic and profoundly affected by environmental humidity. Currently, there is a research gap regarding the impact of traditional processing crafts and natural aging on the hygroscopicity of palm leaf manuscripts. Utilizing dynamic water vapor sorption (DVS), the hygroscopic properties of palm leaves from various years were assessed before and after traditional processing in Yunnan Province, China. The results show that traditional processing slightly increases the equilibrium moisture content (EMC) in environments with 0 to 60% relative humidity (RH), but significantly lowers EMC in high humidity environments, with reductions up to 19.01%. Additionally, hysteresis doubled post-processing, indicating enhanced stability under fluctuating humidity conditions. Sorption models suggest that traditional processing increases the number of adsorption sites while reducing physical adsorption or capillary condensation. FT-IR (Fourier-transform infrared spectroscopy) analysis indicates that the relative contents of cellulose and hemicellulose were reduced by 39.90% and 3.97%, respectively. Degradation occurring in both the crystalline and amorphous regions of cellulose. After natural aging, the hygroscopicity of processed palm leaves improved across the entire humidity range of 0 to 95%, and there was a slight increase in hysteresis. This is due to the increase in both adsorption sites and physical adsorption capabilities. FT-IR results also indicate that the relative contents of cellulose and hemicellulose were decreased by 57.52% and 19.83% after nature aging, respectively. These findings confirm that traditional processing improves the writability and humidity resilience of the leaves, while natural aging enhances their overall hygroscopic properties. This research contributes to our understanding of how humidity damages palm leaf manuscripts. aids in determining optimal RH ranges for storage, and assesses the effectiveness of consolidation treatments in their long–term preservation.

Isoreticular Curves: A Theory of Capillary Condensation To Model Water Sorption within Microporous Sorbents.

Metal-organic frameworks have gained traction as leading materials for water sorption applications due to precise chemical tunability of their well-ordered pores. These applications include atmospheric water capture, heat pumps, desiccation, desalination, humidity control, and thermal batteries. However, the relationships between the framework pore structure and the measurable water sorption properties, namely critical relative humidity for condensation, maximal capacity, and pore size or temperature for the onset of hysteresis, have not been clearly delineated. Herein, we precisely formulate these relationships by application of the theory of capillary condensation and macroscopic thermodynamic models to a large data set of MOF water isotherms. These relationships include a concept termed isoreticular curves that relates the critical pressure for pore condensation (α), gravimetric capacity (Qmax), and hydrophilicity (the Gibbs free energy for binding water, ΔG) as Qmax = a1(ΔG/ln α)2 + a2(ΔG/ln α), with constants a1 and a2 dependent upon the density and volume occupied by the linker and secondary building unit, and framework topology. Through this analysis, we propose guidelines for the maximization of sorption capacity at a given relative humidity with minimal hysteresis and discuss the theoretical limits for capacity at low relative humidity. This model provides an explanation for the lack of high-capacity frameworks at low relative humidity, as increasing pore size also causes an increase in relative humidity. We propose a loose upper bound of Qmax = -0.25(1/ln α)2 - 1.75(1/ln α) for the limit of maximal capacity at a given relative humidity in the dry regime. These guidelines are consequential for the design of new materials for water sorption applications.

Dynamic Change Characteristics and Main Controlling Factors of Pore Gas and Water in Tight Reservoir of Yan’an Gas Field in Ordos Basin

Tight sandstone gas has become an important field of natural gas development in China. The tight sandstone gas resources of Yan’an gas field in Ordos Basin have made great progress. However, due to the complex gas–water relationship, its exploration and development have been seriously restricted. The occurrence state of water molecules in tight reservoirs, the dynamic change characteristics of gas–water two-phase seepage and its main controlling factors are still unclear. In this paper, the water-occurrence state, gas–water two-phase fluid distribution and dynamic change characteristics of different types of tight reservoir rock samples in Yan’an gas field were studied by means of water vapor isothermal adsorption experiment and nuclear magnetic resonance methane flooding experiment, and the main controlling factors were discussed. The results show that water molecules in different types of tight reservoirs mainly occur in clay minerals and their main participation is in the formation of fractured and parallel plate pores. The adsorption characteristics of water molecules conform to the Dent model; that is, the adsorption is divided into single-layer adsorption, multi-layer adsorption and capillary condensation. In mudstone, limestone and fine sandstone, water mainly occurs in small-sized pores with a diameter of 0.001 μm–0.1 μm. The dynamic change characteristics of gas and water are not obvious and no longer change under 7 MPa displacement pressure, and the gas saturation is low. The gas–water dynamic change characteristics of conglomerate and medium-coarse sandstone are obvious and no longer change under 9 MPa displacement pressure. The gas saturation is high, and the water molecules mainly exist in large-sized pores with a diameter of 0.1 μm–10 μm. The development of organic matter in tight reservoir mudstone is not conducive to the occurrence of water molecules. Clay minerals are the main reason for the high water saturation of different types of tight reservoir rocks. Tight rock reservoirs with large pore size and low clay mineral content are more conducive to natural gas migration and occurrence, which is conducive to tight sandstone gas accumulation.

In Ukrainian

The contact wetting is one of the effective methods of studying the adsorption capacity of sorbents. The purpose of the work was to compare the experimentally obtained data on the adsorption capacity of shungite, obtained by the sessile drop method, and the results of modeling the behavior of liquid droplets on heterogeneous surfaces using the Boltzmann lattice method, and to show the suitability of the simplified version of the LBM method that we applied within the framework of a two-dimensional model for modeling complex cases of contact interaction between liquids and sorbent, when it cannot be carried out by the method of contact wetting. The adsorption properties of shungite with regard to the extraction of various impurities from water-alcohol solutions and the capability of the sorbent to recover were investigated by the method of contact wetting and analyzed by involving the data obtained by the methods of nitrogen adsorption, thermogravimetry and IR spectroscopy. It is shown that the adsorption properties of shungite are due to the presence on its surface of hydroxyl functional groups attached to carbon atoms in phenol or enol form, which give the surface hydrophilic characteristics. These groups play a key role in the adsorption of components from the liquid (aqueous) phase due to the formation of a hydrogen bond during the sorption of components from the liquid phase, and are restored after heating in the temperature range of 80–180 °C with the formation of carbon-containing gases and water. It has been found that silanol groups present in shungite do not participate in sorption. Compared to the original shungite sample, the sample after five cycles of adsorption is characterized by a noticeable effect of mass loss (1.8 %) in the temperature range of 80–180 °С. At the same time, the loss of mass is not significant at temperatures below 100 °С. This suggests that the sorbed substances are in the pores and not on the surface of shungite, and they begin to be removed only after heating above 100 °C. The LBM method was used to study fast-moving processes at the meso-level. A comparative analysis of the experimental data obtained by the method of contact wetting with the results of simulation by the Boltzmann lattice method within the framework of the two-dimensional model was carried out. 2D modeling by the LBM method turned out to be an effective means of studying capillary condensation in mesopores, anticipatory wetting of the solid phase, liquid penetration into a porous medium with different topologies, and the formation of anisotropic droplets and anisotropic bridges. The role of mesopores in the sorption process was analyzed by modeling the behavior of liquid droplets on heterogeneous surfaces and using data on the course of adsorption and capillary processes on the surface of a solid phase with different levels of porosity, roughness, and functional composition.

KOH Activated Carbon Coated 3D Wood Solar Evaporator with Highest Water Transport Height and Evaporation Rate for Clean Water Production.

The water evaporation rate of 3D solar evaporator heavily relies on the water transport height of the evaporator. In this work, a 3D solar evaporator featuring a soil capillary-like structure is designed by surface coating native balsa wood using potassium hydroxide activated carbon (KAC). This KAC-coated wood evaporator can transport water up to 32cm, surpassing that of native wood by ≈8 times. Moreover, under 1kWm-2 solar radiation without wind, the KAC-coated wood evaporator exhibits a remarkable water evaporation rate of 25.3kgm-2h-1, ranking among the highest compared with other reported evaporators. The exceptional water transport capabilities of the KAC-coated wood should be attributed to the black and hydrophilic KAC film, which creates a porous network resembling a soil capillary structure to facilitate efficient water transport. In the porous network of coated KAC film, the small internal pores play a pivotal role in achieving rapid capillary condensation, while the larger interstitial channels store condensed water, further promoting water transport up more and micropore capillary condensation. Moreover, this innovative design demonstrates efficacy in retarding phenol from wastewater through absorption onto the coated KAC film, thus presenting a new avenue for high-efficiency clean water production.

ОПРЕДЕЛЕНИЕ ИНТЕГРАЛЬНОЙ И ДИФФЕРЕНЦИАЛЬНОЙ ПОРИСТОСТИ ЖАРОСТОЙКИХ БЕТОНОВ УСОВЕРШЕНСТВОВАННЫМ МЕТОДОМ КАПИЛЛЯРНОЙ КОНДЕНСАЦИИ

The article discusses the method developed by the authors for assessing the distribution of pores by their sizes, which consists in obtaining a desorption isotherm of a material that is previously completely saturated with liquid sorbate, which fills all the pores of the material. In this case, complete saturation is achieved not in the process of capillary condensation, but by saturation of the material during vacuuming.

Polyaniline/Graphene oxide composite as an Ultra-Sensitive humidity sensor

This paper investigated the humidity-sensing response of polyaniline/Graphene oxide (PGO) composites. Graphene oxide (GO) was synthesised using the improvised hummers method, and polyaniline (PANI) was synthesised using the chemical in-situ polymerisation process. By adding different weights per cent (wt%) of Graphene oxide (GO) to the polymer matrix, PGO composites were prepared. Structural and morphological properties of GO were confirmed by XRD, RAMAN, FTIR, SEM, EDX, and HR-TEM (elementary mapping) characterisations. The XRD, FTIR SEM and EDX proficiencies were employed to characterise the PGO composites. To experience the humidity response performance, the film of PANI, GO, and PGO samples was groomed by wedging the sample on an IDT substrate using a drop casting technique. Among the samples, the PGO-3 composite (polyaniline/Graphene oxide 15 wt%) depicted a maximum sensing response (SH) of 93.4 % with a dynamic timing behaviour of 4 s and 7 s. The Nobel characters, such as low accurate Sensing response, fewer detection limits (LOD), negligible hysteresis and perfect stability, were observed in the PGO-3 composite. The physical properties such as porosity, water content, and degree of swelling have been outstandingly enhanced in the PGO-3 composite compared to PANI and GO. The mechanism for sensing the PGO-3 composites was deliberately explained based on establishing superficial physisorption, chemisorption layers, and later capillary condensation.

Sorption Hysteresis: A Statistical Thermodynamic Fluctuation Theory.

Hysteresis is observed commonly in sorption isotherms of porous materials. Still, there has so far been no unified approach that can both model hysteresis and assess its underlying energetics. Standard approaches, such as capillary condensation and isotherms based on interfacial equations of state, have not proved to be up to the task. Here, we show that a statistical thermodynamic approach can achieve the following needs simultaneously: (i) showing why adsorption and desorption transitions may be sharp yet continuous; (ii) providing a simple (analytic) isotherm equation for hysteresis branches; (iii) clarifying the energetics underlying sorption hysteresis; and (iv) providing macroscopic and nanoscopic perspectives to understanding hysteresis. This approach identifies the two pairs of parameters (determinable by fitting experimental data) that are required to describe the hysteresis: the free energy per molecule within the pore clusters and the cluster size in the pores. The present paper focuses on providing mechanistic insights to IUPAC hysteresis types H1, H2(a), and H2(b) and can also be applied to the isotherm types IV and V.

Cross-Polarization Solid-State NMR Quantification of Species within Pores of Metal-Organic Frameworks: A Case Study of α-Mg3(HCOO)6.

The quantitative measurement of adsorbed guest species within metal-organic framework (MOF) pores is of fundamental importance for evaluating the adsorption performance of MOFs. However, routine analytic techniques such as thermogravimetric analysis cannot distinguish the contribution from species adsorbed within pores, species adsorbed on the surface, and gas phase or liquid phase encapsulated in the inter-crystalline space. Herein, we developed a new quantification method based on the cross-polarization (CP) solid-state nuclear magnetic resonance (ssNMR) technique, in which only the species within MOF pores are selectively probed due to the dramatically reduced mobility. Using the commercialized MOF α-Mg3(HCOO)6 as an example, a good linear correlation between Areaguest/Areaframework (i. e., the integrated area of guest and framework 13C NMR signals) and guest loading can be observed for several representative molecules such as benzene, tetrahydrofuran (THF), and 1,4-dioxane, clearly revealing the feasibility of CP quantification approach. The effects of guest molecule and corresponding residual mobility on the CP quantification are further discussed by varying the geometry and size of guest molecules. This methodology thus provides an effective and irreplaceable route to evaluate the adsorption performance of porous materials in-depth, especially for liquid-phase adsorption and gas-phase adsorption in which the capillary condensation is not negligible.

Capillary Condensation Mediated Fluidic Straining for Enhanced Bacterial Inactivation

AbstractBiomaterials capable of continuously inactivating pathogens are essential for suppressing transmission of infectious diseases, such as epidemic cerebrospinal meningitis and pulmonary tuberculosis. Here, capillary condensation of air moisture within nano‐confined spaces between superhydrophilic rigid nanorods is shown and target microbiology spontaneously stretch and inactivate aerosolized microorganisms. Specifically, the negative Gaussian curvature‐shaped water condensate causes fluidic straining, comprising surface tension and Laplace pressure, strong enough to deform and eliminate the selected bacteria. Plate counting quantifies the sharply reduced contact‐killing period for superhydrophilic and bare nanorods (6 vs 100 min for E. coli, 20 vs 120 min for S. aureus) under relative humidity of 70%. Theoretical calculations and experimental studies indicate increased mechanical straining and mechano‐bactericidal by improving air moisture content. To further illustrate utility, long‐term antibacterial medical masks are fabricated by integrating such nanorods onto commercial fabrics. Collectively, these findings highlight the immense potential of capillary condensation‐induced fluidic straining as an eco‐friendly, broad‐spectrum, and highly efficient antibacterial strategy.

Impact of relative humidity variations on Carrara marble mechanical properties investigated by nonlinear resonant ultrasound spectroscopy

Like many other stones, marble mechanical properties can be significantly changed in presence of water. Water most often induces a weakening which can lead to marble degradation when coupled to temperature variations. Yet, marble artefacts are more frequently subjected to relative humidity (RH) variations than episodes of water imbibition and/or drastic temperature variations. Thus, one could wonder how do variations of RH alone impact marble mechanical state. In this study, Carrara Gioia marble samples are subjected to adsorption-desorption cycles. They were previously thermally-damaged between 40 and 105 °C, and their microstructure was characterized for each heating temperature. The evolution of their mechanical properties is monitored non-destructively with two parameters measured by Nonlinear Resonant Ultrasound Spectroscopy. The resonant frequency decreases weakly with increasing RH, indicating a diminution in sample stiffness due to low moisture-induced softening. The nonlinear parameter increases strongly, probably due to higher capillary pressure associated to a capillary condensation increase with RH. However, these phenomena are reversible: during adsorption-desorption cycling both parameters remain quite constant for a given RH. Therefore, while a RH increase impacts the mechanical properties of Carrara marble, adsorption-desorption cycling shows a reversible behavior which does not induce any permanent change in mechanical properties.

Capillary condensation between nonparallel walls.

We study the condensation of fluids confined by a pair of nonparallel plates of finite height H. We show that such a system experiences two types of condensation, termed single and double pinning, which can be characterized by one (single-pinning) or two (double-pinning) edge contact angles describing the shape of menisci pinned at the system edges. For both types of capillary condensation, we formulate the Kelvin-like equationand determine the conditions under which the given type of condensation occurs. We construct the global phase diagram revealing a reentrant phenomenon pertinent to the change of the capillary condensation type upon varying the inclination of the walls. Asymptotic properties of the system are discussed and a link with related phase phenomena in different systems is made. Finally, we show that the change from a single- to a double-pinned state is a continuous transition, the character of which depends on the wetting properties of the walls.

Capillary Condensation of Water in Graphene Nanocapillaries.

Recent experiments have revealed that the macroscopic Kelvin equation remains surprisingly accurate even for nanoscale capillaries. This phenomenon was so far explained by the oscillatory behavior of the solid-liquid interfacial free energy. We here demonstrate thermodynamic and capillarity inconsistencies with this explanation. After revising the Kelvin equation, we ascribe its validity at nanoscale confinement to the effect of disjoining pressure. To substantiate our hypothesis, we employed molecular dynamics simulations to evaluate interfacial heat transfer and wetting properties. Our assessments unveil a breakdown in a previously established proportionality between the work of adhesion and the Kapitza conductance at capillary heights below 1.3 nm, where the dominance of the work of adhesion shifts primarily from energy to entropy. Alternatively, the peak density of the initial water layer can effectively probe the work of adhesion. Unlike under bulk conditions, high confinement renders the work of adhesion entropically unfavorable.

Using industrial waste in porous building materials for indoor humidity control

This study uses waste bricks and waste catalyst as raw materials in the synthesis of humidity control building materials with high structural strength. This paper explores the feasibility of producing porous humidity control materials (PHCM) through the billet sintering of waste brick with various quantities of waste catalyst (0 %–40 %) for indoor construction. N2 adsorption and desorption isotherms revealed that PHCM exhibits Type-IV adsorption with H3 hysteresis loops, indicating a network of interconnected mesopores with diameters ranging from 3 to 17 nm. Humidity control analysis revealed that increasing the waste catalyst content significantly enhanced the equilibrium moisture content and moisture adsorption and desorption capacity. This study determined that the adsorption of moisture within the PHCM relies on capillary condensation within the mesopores. Under 95 % relative humidity (RH), the highest equilibrium moisture content (2.97 kg/kg) and 12-h moisture adsorption capacity (72.41 g/m2) were obtained in specimens prepared at a sintering temperature of 1000 °C with a 40 % spent catalyst. This excellent adsorption capacity can be attributed to the high surface area of the waste catalyst, which increased the surface area of PHCM from 0.013 to 8.529 m2/g. This study demonstrates the benefits of synthesizing PHCM using waste bricks and catalysts in terms of porous properties, mechanical properties, and humidity control performance.