Interconnected Pore System Research Articles

A Study of CO2 Storage in Bimodal Carbonate Aquifer Rocks: Challenges and Enhancement through Foaming

Summary In carbonate rock reservoirs, the presence of dual-pore systems, characterized by two distinct pore size distributions, plays a crucial role in gas storage in saline aquifers. However, comprehensive research on the impact of bimodal porosity on CO2 storage in such reservoirs is lacking. This study explores CO2 storage efficiency in carbonate aquifer rocks with bimodal porosity. Petrographic examination, capillary pressure measurements, and nuclear magnetic resonance (NMR) T2 profiling revealed two distinct and interconnected pore systems with equal effective porosity proportions. While both systems facilitated fluid flow, the micropores had a high capillary entry pressure (>100 psi). Coreflood experiments showed gas displacement efficiencies below 50%, primarily in larger pores, with only 49–58% of these large pores (20–28% of total pores) storing injected gas through residual trapping after water imbibition. To address this challenge, CO2 was foamed using a foaming agent to enhance viscous forces and overcome capillary forces. This resulted in significant improvements, including a 31% increase in displacement efficiency and a 28% increase in residual gas. NMR analysis revealed effective redirection of CO2 into smaller pores when foam was applied. In another experiment on a sample with a different pore geometry, the use of nanoparticles to strengthen foam increased sweep efficiency by up to 117%, with a corresponding increase of up to 169% in residual trapping. While the use of foam entails additional operational expenses, we contend that the economic viability of foam technology for CO2 storage hinges on a rigorous cost-benefit analysis that weighs increased storage capacity/security against chemical costs. Such analysis should also consider the time, cost, and uncertainty associated with developing additional storage sites. Furthermore, improved site selection criteria in carbonate rocks are needed, including a predictive model for T2 cutoff to identify aquifers with excessive micropores and avoid them during site selection. While fractured porosity is not within the scope of this study, it is expected that foam can equally improve sweep and trapping efficiencies in naturally fractured carbonate rocks.

Low-temperature cordierite ceramics with porous structure for thermal shock resistance products

This article shows the results of the study of low-temperature (1100−1150 °C) porous ceramics of cordierite composition. The technological manufacturing parameters, the features of the microstructural and phase composition of ceramics have been studied. A decrease in the sintering temperature is achieved by appending a part of components using eutectic glass of MgO–Al2O3–SiO2 pseudoternary system. The principle of reactive formation of the structure of the ceramic sample is implemented in the process of its low-temperature firing. The formation of α-cordierite occurs in the process of firing ceramics by means of intensive interaction between eutectic glass components and crystalline fillers, as well as in the result of glass crystallization. By means of the thin layers of the glassy phase, cordierite crystals form a hard base with a branched system of interconnected open pores (30.0−31.3 %). The cordierite-phase crystals, forming the structure of ceramics, have a particle size ranging from 0.2 to 0.3 μm to 1.0−2.0 μm. The specific surface area of the porous cordierite ceramics is in the range of 4.2–4.7 m2/g. The developed cordierite ceramics is characterized by its low coefficient of linear temperature expansion (1.7–2.6)·10−6 °С−1, which determines its high thermal shock resistance (1000−1150°С). The ceramics may be used as filtering elements in high-temperature filtering units, as well as catalyst carriers in the exhaust systems of combustion engines for discharging the sooty component.

Enabling hydrate-based methane storage under mild operating conditions by periodic mesoporous organosilica nanotubes

Biomethane is a renewable natural gas substitute produced from biogas. Storage of this sustainable energy vector in confined clathrate hydrates, encapsulated in the pores of a host material, is a highly promising avenue to improve storage capacity and energy efficiency. Herein, a new type of periodic mesoporous organosilica (PMO) nanotubes, referred to as hollow ring PMO (HR-PMO), capable of promoting methane clathrate hydrate formation under mild working conditions (273 K, 3.5 MPa) and at high water loading (5.1 g water/g HR-PMO) is reported. Gravimetric uptake measurements reveal a steep single-stepped isotherm and a noticeably high methane storage capacity (0.55 g methane/g HR-PMO; 0.11 g methane/g water at 3.5 MPa). The large working capacity throughout consecutive pressure-induced clathrate hydrate formation-dissociation cycles demonstrates the material’s excellent recyclability (97% preservation of capacity). Supported by ex situ cryo-electron tomography and x-ray diffraction, HR-PMO nanotubes are hypothesized to promote clathrate hydrate nucleation and growth by distribution and confinement of water in the mesopores of their outer wall, along the central channels of the nanotubes and on the external nanotube surface. These findings showcase the potential for application of organosilica materials with hierarchical and interconnected pore systems for pressure-based storage of biomethane in confined clathrate hydrates.

Pore Structure Tuning of Poly-EGDMA Biomedical Material by Varying the O-Quinone Photoinitiator.

Porous polymer monoliths with thicknesses of 2 and 4 mm were obtained via polymerization of ethylene glycol dimethacrylate (EGDMA) under the influence visible-light irradiation in the presence of a 70 wt% 1-butanol porogenic agent and o-quinone photoinitiators. The o-quinones used were: 3,5-di-tret-butyl-benzoquinone-1,2 (35Q), 3,6-di-tret-butyl-benzoquinone-1,2 (36Q), camphorquinone (CQ), and 9,10-phenanthrenequinone (PQ). Porous monoliths were also synthesized from the same mixture but using 2,2'-azo-bis(iso-butyronitrile) (AIBN) at 100 °C instead o-quinones. According to the results of scanning electron microscopy, all the resulting samples were conglomerates of spherical, polymeric particles with pores between them. Use of mercury porometry showed that the interconnected pore systems of all the polymers were open. The average pore size, Dmod, in such polymers strongly depended on both the nature of the initiator and the method of initiation of polymerization. For polymers obtained in the presence of AIBN, the Dmod value was as low as 0.8 μm. For polymers obtained via photoinitiation in the presence of 36Q, 35Q, CQ, and PQ, the Dmod values were significantly greater, i.e., 9.9, 6.4, 3.6, and 3.7 μm, respectively. The compressive strength and Young's modulus of the porous monoliths increased symbatically in the series PQ < CQ < 36Q < 35Q < AIBN with decreasing proportions of large pores (over 12 μm) in their polymer structures. The photopolymerization rate of the EGDMA and 1-butanol, 30:70 wt% mixture was maximal for PQ and minimal for 35Q. All polymers tested were non-cytotoxic. Based on the data from MTT testing, it can be noted that the polymers obtained via photoinitiation were characterized by their positive effect on the proliferative activity of human dermal fibroblasts. This makes them promising osteoplastic materials for clinical trials.

Porogen Concentration Effect on the Pore Structure and Properties Evolution of Polymer Monolith Based on Oligocarbonate Dimethacrylate OCM-2.

Porous polymer monolith materials of 2-mm thickness were obtained by visible light-induced radical polymerization of oligocarbonate dimethacrylate (OCM-2) in the presence of 1-butanol (10 to 70 wt %) as a porogenic additive. The pore characteristics and morphology of polymers were studied by mercury intrusion porosimetry and scanning electron microscopy. Monolithic polymers with both open and closed pores up to 100 nm in size are formed when the alcohol content in the initial composition is up to 20 wt %. The pore structure in such materials is a system of holes in the bulk of the polymer (hole-type pores). Open interconnected pores with a specific volume up to 2.22 cm3/g and modal pore size up to 10 microns are formed in the volume of the polymer with 1-butanol content of more than 30 wt %. Such porous monoliths are a structure of covalently bonded polymer globules (interparticle-type pores). The free space between the globules represents a system of open interconnected pores. In the transition region of 1-butanol concentrations (from 20 to 30 wt %), areas with both structures and intermediate frameworks, as well as honeycomb structures of polymer globules connected by bridges, are fixed on the polymer surface. It was found that the transition from one type of pore system to another is accompanied by a sharp change in the strength characteristics of the polymer. Approximation of experimental data using the sigmoid function made it possible to determine the concentration of the porogenic agent in the vicinity of which the percolation threshold is observed.

Large‐Scale and Controllable Syntheses of Covalently‐Crosslinked Poly(ionic liquid) Nanoporous Membranes

AbstractHerein, we report an exciting synthetic procedure for the scalable and controllable fabrication of covalently crosslinked poly(ionic liquid) (PIL) nanoporous membranes (CPILMs) in water solution under ambient conditions. We found that the pore sizes, flexibility and compositions of freestanding CPILMs can be finely tailored by a rational structural choice of PIL, diketone and aldehyde. Studies on the CPILM formation mechanism revealed that hydrogen bonding‐induced phase separation of amino‐functionalized homo‐PIL between its polar and apolar domains coupled with structural rearrangements due to the Debus Radsizewski reaction‐triggered ambient covalent crosslinking process created a stable three‐dimensionally interconnected pore system in water solution. Employing structurally stable CPILMs in ion sieving devices resulted in an excellent Li+/Mg2+ separation efficiency due to the positively charged nature and “Donann” effects. This green, facile yet versatile approach to the production of CPILMs is a conceptually distinct and commercially interesting strategy for making useful nanoporous functional polyelectrolyte membranes.

Large-Scale and Controllable Synthesis of Covalently-Crosslinked Poly(ionic liquid) Nanoporous Membranes.

Herein, we report an exciting synthetic procedure for the scalable and controllable fabrication of covalently crosslinked poly(ionic liquid) (PIL) nanoporous membranes (CPILMs) in water solution under ambient conditions. We found that the pore sizes, flexibility and compositions of freestanding CPILMs can be finely tailored by a rational structural choice of PIL, diketone and aldehyde. Studies on the CPILM formation mechanism revealed that hydrogen bonding-induced phase separation of amino-functionalized homo-PIL between its polar and apolar domains coupled with structural rearrangements due to the Debus Radsizewski reaction-triggered ambient covalent crosslinking process created a stable three-dimensionally interconnected pore system in water solution. Employing structurally stable CPILMs in ion sieving devices resulted in an excellent Li+/Mg2+ separation efficiency due to the positively charged nature and "Donann" effects. This green, facile yet versatile approach to the production of CPILMs is a conceptually distinct and commercially interesting strategy for making useful nanoporous functional polyelectrolyte membranes.

Record Ultralarge-Pores, Low Density Three-Dimensional Covalent Organic Framework for Controlled Drug Delivery.

The unique structural characteristics of three-dimensional (3D) covalent organic frameworks (COFs) like high surface areas, interconnected pore system and readily accessible active sites render them promising platforms for a wide set of functional applications. Albeit promising, the reticular construction of 3D COFs with large pores is a very demanding task owing to the formation of interpenetrated frameworks. Herein we report the designed synthesis of a 3D non-interpenetrated stp net COF, namely TUS-64, with the largest pore size of all 3D COFs (47 Å) and record-low density (0.106 g cm-3 ) by reticulating a 6-connected triptycene-based linker with a 4-connected porphyrin-based linker. Characterized with a highly interconnected mesoporous scaffold and good stability, TUS-64 shows efficient drug loading and controlled release for five different drugs in simulated body fluid environment, demonstrating the competency of TUS-64 as drug nanocarriers.

Record Ultralarge‐Pores, Low Density Three‐Dimensional Covalent Organic Framework for Controlled Drug Delivery**

AbstractThe unique structural characteristics of three‐dimensional (3D) covalent organic frameworks (COFs) like high surface areas, interconnected pore system and readily accessible active sites render them promising platforms for a wide set of functional applications. Albeit promising, the reticular construction of 3D COFs with large pores is a very demanding task owing to the formation of interpenetrated frameworks. Herein we report the designed synthesis of a 3D non‐interpenetrated stp net COF, namely TUS‐64, with the largest pore size of all 3D COFs (47 Å) and record‐low density (0.106 g cm−3) by reticulating a 6‐connected triptycene‐based linker with a 4‐connected porphyrin‐based linker. Characterized with a highly interconnected mesoporous scaffold and good stability, TUS‐64 shows efficient drug loading and controlled release for five different drugs in simulated body fluid environment, demonstrating the competency of TUS‐64 as drug nanocarriers.

Impacts of Depositional Facies and Diagenesis on Reservoir Quality: A Case Study from the Rudist‐bearing Sarvak Formation, Abadan Plain, SW Iran

AbstractAn integrated geological‐petrophysical analysis of the rudist‐bearing sequence of the Cretaceous Sarvak Formation is given one giant oilfield, and provides an improved understanding of this main reservoir in the Abadan Plain, in the Zagros Basin, SW Iran. The main objective of this study is to evaluate reservoir potential of the Sarvak Formation, and then to utilize the calibrated well log signature to correlate reservoir potential in un‐cored wells. Eight main facies are recognized and categorized in five facies groups: lagoon, shoal, rudist‐biostrome, slope, and shallow open marine, deposited on a shelf carbonate platform. Given the distribution of diagenetic products and their effects on pore systems, three diagenetic facies namely, (DF‐1) low dissolution and cementation; (DF‐2); high dissolution; and (DF‐3) high cementation are differentiated. The initial sedimentary characteristics in combination with distribution of diagenetic products play an important role in reservoir quality heterogeneity. The effect of diagenetic processes related to disconformities mainly depends on the facies nature below these surfaces. Grain‐dominated facies of shoal and rudist debris, observed below the Cenomanian–Turonian disconformity, are mostly characterized by high dissolution and interconnected pore systems. Finally, depositional and diagenetic facies in the studied wells are correlated by petrophysical well log data, leading to distribution of the reservoir zones. Data obtained can be utilized for efficient reservoir characterization of the Sarvak Formation and its equivalent units in the Arabian Plate.

Use of Cement Mortar Incorporating Superabsorbent Polymer as a Passive Fire-Protective Layer

Concrete structures, when exposed to fire or high temperatures for a certain time, could suffer partial damage or complete structural failure. Passive fire-protective coating materials are an alternative way to prevent or delay damage to concrete structures resulting from fire. Superabsorbent polymer (SP) is a synthetic material known for its ability to absorb and retain a large volume of water within itself. With this unique property, the SP exhibits great potential for use as a passive fire protection material. Although several studies have been carried out to investigate the effect of SP as a surface coating material for fire protection, very few have been investigated on the potential use of SP mixed with mortar as a passive fire-protective layer. The objective of this study is to introduce the use of SP in plastering mortar as a fire-protective layer for concrete subjected to temperatures up to 800 °C. This study is divided into two parts: (1) investigating the properties of cement mortar mixed with SP at 0.5% (CONC/SP-0.5) and 1.0% (CONC/SP-1.0) by weight of cement, and (2) investigating the potential use of SP mortar as a plastering layer for concrete subject to high temperatures. The experimental results showed that the density and compressive strength of SP mortar decreases with increasing SP dosages. From the heat exposure results, SP mortar exhibited lower strength loss due to the ability to mitigate moisture through its interconnected pore system. As for the use of SP mortar as a plastering layer, the results demonstrated the concrete specimen plastered with SP mortar had a lower temperature at the interface and core than that plastered with plain mortar. This led to a reduced strength loss of 20.5% for CONC/SP-0.5 and 17.2% for CONC/SP-1.0.

Copper-catalyzed FeOOH templated method for accelerated fabrication of ultraporous membranes used in microalgae dewatering

Porous materials including polymeric and inorganic membranes are important and widely used in various industries. Controlling the pore size and pore distribution in porous materials is the major focus in this field. In this study, a novel copper-catalyzed template dissolution approach using ferric oxyhydroxide (FeOOH) as nano-templates was introduced for the preparation of ultraporous polymeric membrane. Compared to typically used acid dissolution method, this approach accelerated the removal of FeOOH by 30 folds. The reduction of ferric by copper into ferrous weakened the Fe-O bonds in FeOOH hence leading to fast dissolution of the nanomaterials. The effectiveness of copper-catalyzed FeOOH dissolution was affected by the concentration of acid and copper ions as well as the type of anions present in the dissolution solution. Membranes fabricated via FeOOH-templating approach were evaluated for microalgae dewatering application and showed 8–21 % higher solution flux than their corresponded nanocomposite membrane. The enhancement was attributed to the elevation of membrane porosity by 1–4 % and the creation of more interconnected pore system. The best membrane, M1.0 exhibited the highest porosity of 94 % and achieved the best microalgae solution flux of 57.7 L·m−2·h−1. The outcomes of this study confirmed the viability of copper-catalyzed approached in accelerating the formation of ultraporous materials and demonstrated the potential of such materials in microalgae dewatering application.

Development of Pore Morphology During Nitrate Group Removal by Calcination of Mesoporous CexZr1-x-y-zYyLazO2-δ Powders.

Here, we present a study of the development of the micro- and mesoporosity of a CexZr1-x-y-zYyLazO2-δ oxygen storage material upon treatment at temperatures up to 1050 °C. The investigated powder, obtained from nitrate-based metal oxide precursors in a specially developed hydrothermal synthesis, is highly crystalline, features a high surface area and does not show phase segregation at high temperatures. By employing an advanced methodology, consisting of state-of-the-art argon physisorption, thermogravimetric analysis coupled with mass spectrometry (TG-MS) and X-ray powder diffraction (XRD) along with Raman spectroscopy, we correlate the stability of the mesopore system to the presence of surface-bound nitrate groups introduced during synthesis, which prevent sintering up to a temperature of 600 °C. In addition, the connectivity of mesopores was further studied by hysteresis scanning within the argon physisorption measurements. These advanced physisorption experiments suggest a three-dimensionally interconnected pore system and, in turn, a 3D network of the material itself on the nanometer scale which appears to be beneficial to endow the mesopore space with enhanced stability against sintering and mesopore collapse once the removal of nitrate groups is completed.

Advanced solid-phase extraction of tetravalent actinides using a novel hierarchically porous functionalized silica monolith

Separation of actinides is of great concern from the perspective of nuclear energy development and environmental issues, and the development of a highly efficient solid-phase extraction (SPE) process holds significant promise for actinide separation. However, the slow mass transfer kinetics in the currently available SPE separation media limited the throughput and efficiency, rendering the separation process more challenging. Hierarchically porous structures with well-organized and highly interconnected pore systems have been shown to provide efficient mass transfer and enhanced performance in nature. Herein, this paper reports the synthesis of a crack-free diglycolamic acid-functionalized silica monolith with hierarchical macro and meso porous structure for SPE. The hierarchically porous structures were retained upon mild modifications, which favored the convective mass transport and provided more binding sites, resulting in fast kinetics and high throughput. The separation ability was evaluated based on the separation and recovery of Th(IV) from a complex matrix. A superior Th(IV) separation performance (Kd > 2.6 × 104 mL/g) was achieved in the presence of alkaline earth metals, rare earth elements, and uranium within 1 min by batch sorption, and the maximum separation coefficients of Th(IV)/Ln(III) and Th(IV)/U(VI) exceed 1000 and 140, respectively. Particularly, the synthesized material allowed the separation of Th from monazite leachates with highly efficient recovery (> 96%) at a high flow rate (5 mL/min) by column study. Investigation of the binding mechanism revealed the formation of a stable coordination complex (Th(NO3)L3) via Th−O bonds. The material was also employed for the extraction of Pu(IV), and satisfactory sorption was achieved. Thus, this new functionalized material has potential application prospects for an improved actinide separation process.

Diffusivity of ethylammonium nitrate protic ionic liquid confined in porous glasses

We studied the diffusion of ionic liquid ethylammonium nitrate confined within pores of two types of porous glass, Vycor and Varapor, with average pore sizes of 4 nm and 9.8 nm, respectively, by 1H NMR in the temperature range of 295–325 K. The diffusional behavior of the ionic liquid corresponds to long-term diffusion in a system of interconnected pores. It was shown that the diffusivity of EAN confined in Varapor is controlled by the porous system’s tortuosity and does need to take into consideration the interaction with the surface of the discrete pore walls. In the case of Vycor, the long-term diffusivity is a factor 1.5 lower than that expected in the absence of interaction with the pore walls. Two possible mechanisms that may explain this discrepancy are the EAN-surface interaction and retardation of EAN diffusion compared to n-decane in smaller pores present in Vycor porous glass due to pore size distribution. Confinement of EAN in nanoporous glass does not leads to the EAN phase transformation observed earlier for alkylammonium nitrates enclosed in a micrometer-sized layer. Prolonged exposure of EAN to a strong static magnetic field does not leads to changes in the NMR and diffusivity of EAN over time.

MOLDABLE AND MACHINABLE POROUS CARBON STRUCTURES OBTAINED FROM WHEY

A new porous carbon structures made by sintering whey powder in a mold at 150ºC and subsequent carbonization and/or activation are described. These porous carbon structures represent a step beyond simple activated carbon monoliths, as they can take the shape of any mold and machined if necessary. These carbon materials have a porosity that can reach up 70%, made up of a system of hierarchical and interconnected pores, which gives them a high permeability. Furthermore, they have a much higher mechanical strength than other porous carbon monoliths. Key Words: carbon structures, monoliths, porous carbon, activated carbon, machining, sintering, whey, whey powder.

Design and Assessment of Biodegradable Macroporous Cryogels as Advanced Tissue Engineering and Drug Carrying Materials.

Cryogels obtained by the cryotropic gelation process are macroporous hydrogels with a well-developed system of interconnected pores and shape memory. There have been significant recent advancements in our understanding of the cryotropic gelation process, and in the relationship between components, their structure and the application of the cryogels obtained. As cryogels are one of the most promising hydrogel-based biomaterials, and this field has been advancing rapidly, this review focuses on the design of biodegradable cryogels as advanced biomaterials for drug delivery and tissue engineering. The selection of a biodegradable polymer is key to the development of modern biomaterials that mimic the biological environment and the properties of artificial tissue, and are at the same time capable of being safely degraded/metabolized without any side effects. The range of biodegradable polymers utilized for cryogel formation is overviewed, including biopolymers, synthetic polymers, polymer blends, and composites. The paper discusses a cryotropic gelation method as a tool for synthesis of hydrogel materials with large, interconnected pores and mechanical, physical, chemical and biological properties, adapted for targeted biomedical applications. The effect of the composition, cross-linker, freezing conditions, and the nature of the polymer on the morphology, mechanical properties and biodegradation of cryogels is discussed. The biodegradation of cryogels and its dependence on their production and composition is overviewed. Selected representative biomedical applications demonstrate how cryogel-based materials have been used in drug delivery, tissue engineering, regenerative medicine, cancer research, and sensing.

Porous Polymer Scaffolds based on Cross-Linked Poly-EGDMA and PLA: Manufacture, Antibiotics Encapsulation, and In Vitro Study.

Porous polymer materials derived from poly(ethylene glycol dimethacrylate) (poly-EGDMA) and antibiotic containing polylactide (PLA) are obtained for the first time. Porous poly-EGDMA monoliths with a system of open interconnected pores are synthesized by a visible light-induced radical polymerization of EGDMA in the presence of 70wt% of porogenic agent, e.g., 1-butanol, 1-hexanol, 1-octanol, or cyclohexanol. The porosity of the obtained polymers is 75-78%. A modal pore size depends on the nature of the porogen and varies from 0.5µm (cyclohexanol) to 12µm (1-butanol). The polymer matrix made with 1-butanol features the presence of pores ranging from 1 to 100µm. The pore surface of poly-EGDMA matrices is inlayered with poly-D,L-lactide (Mn 23 × 103 Da, PDI1.31). The PLA-modified poly-EGDMA retains a porous structure that is similar to the initial poly-EGDMA but with improved strength characteristics. The presence of antibiotic containing PLA ensures a high and continuous antibacterial activity of the hybrid polymeric material for 7 days. The nontoxicity of all the porous matrices studied makes them promising for clinical tests as osteoplastic materials.

The effect of interconnections on gas adsorption in materials with spherical mesopores: A Monte Carlo simulation study.

Gas adsorption is a standard method for measuring pore-size distributions of nanoporous materials. This method is often based on assuming the pores as separate entities of a certain simple shape: slit-like, cylindrical, or spherical. Here, we study the effect of interconnections on gas adsorption in materials with spherical pores, such as three-dimensionally ordered mesoporous (3DOm) carbons. We consider interconnected systems with two, four, and six windows of various sizes. We propose a simple method based on the integration of solid-fluid interactions to take into account these windows. We used Monte Carlo simulations to model argon adsorption at the normal boiling point and obtained adsorption isotherms for the range of systems. For a system with two windows, we obtained a remarkably smooth transition from the spherical to cylindrical isotherm. Depending on the size and number of windows, our system resembles both spherical and cylindrical pores. These windows can drastically shift the point of capillary condensation and result in pore-size distributions that are very different from the ones based on a spherical pore model. Our results can be further used for modeling fluids in a system of interconnected pores using Monte Carlo and density functional theory methods.

A green chemical approach for synthesis of sponge-like mesoporous gamma alumina and evaluation of three parameters OH/Al, salt concentration and ageing time on BET and BJH properties

Synthetic strategies to control the properties of gamma-alumina mesoporous have been discussed. In this study, the emphasis is placed upon the effect of three parameters pH of the reaction, salt precursor concentration and ageing time on the pore structure of nanoparticles synthesized by precipitation method. The gamma alumina as the only phase was recognized due to the appearance of characteristic peaks based on standard data JCPDS 29-0063 card in XRD pattern. The samples were analyzed by BET and BJH analysis in terms of specific surface area and pore structure (size distribution, morphology, and total pore volume). The results showed that all the synthesized samples are mesoporous. The sample synthesized at a precursor concentration of 0.1 M and pH 8 and the ageing time of 48 h obtained the highest specific surface area (217.02 m2 g−1) among all samples, while the sample prepared at the precursor concentration 0.2 M and pH 8 showed the highest pore volume with a value of 0.31 cm3 g−1. Among the parameters, only pH altered the pore morphologies from spherical to cylindrical while the ageing time and salt concentration did not change the pore morphology of mesoporous alumina samples. The TEM image reveals the sponge-like morphology which implies the appearance of a highly inter-connected pore system.