가스 분리막은 에너지 효율적인 가스 정제와 탄소 포집을 위한 핵심 기술이지만, 기존의 고분자 분리막은 투과도 와 선택도 사이의 상충관계를 피하기 어렵다. 이러한 한계를 극복하기 위해 다공성 소재가 유망한 대안으로 주목받고 있다. 본 리뷰에서는 가스 분리막 분야에서 최근 활발히 연구되고 있는 주요 다공성 소재인 금속-유기 골격체(MOFs), 제올라이트, 그리고 기타 다공성 소재에 대한 연구 동향을 정리한다. 조절 가능한 기공 구조를 갖는 MOF는 혼합매질 막(MMMs)에 필러 또는 단독 막 형태로 적용되어 선택도와 투과도를 향상시킨다. 제올라이트는 우수한 분자체 성능과 높은 내구성을 바탕으로 까다로운 분리 공정에서도 탁월한 성능을 보인다. 또한 다양한 차세대 다공성 소재 는 기존의 한계를 뛰어넘는 성능을 구현 할 수 있는 분리막 재료로 평가된다. 최근 연구들은 다공성 필러를 도입하거나 다공성 구조를 지닌 매트릭스를 설계함으로써, 기존 고분자 분리막의 한계를 넘어서는 높은 선택도와 투과도를 동시에 달성할 수 있음을 보여준다. 본 리뷰는 다공성 소재 기반 고성능 가스 분리막 연구의 최신 동향을 정리하고, 향후 발전 방향에 대한 통찰을 제공하는 데 목적이 있다.

The high value-added utilization of traditional coal resources is one of the important ways to achieve the strategic goals of carbon peaking and carbon neutrality. Simultaneously, coal-based carbon materials, noted for their cost-effectiveness, superior conductivity, and inherent stability, are emerging as promising candidates for next-generation capacitor technologies. This research presents a series of coal-derived porous carbon by pyrolysis using low rank lignite as raw material and KOH as activator, which are employed in symmetrical supercapacitors filled with liquid electrolytes. The physicochemical properties of the as-prepared electrode materials are characterized by means of scanning electron microscopy, X-ray diffraction, Raman spectroscopy, and their supercapacitive performance are evaluated through cyclic voltammetry and galvanostatic charge–discharge tests. The coal-based porous carbon electrode prepared at an activation temperature of 800 °C (KOH-800) exhibits a specific capacitance of 142.2 F g− 1 at a current density of 1 A g− 1, and retaining 80% of its capacitance (114.0 F g− 1) even at 10 A g− 1. The fabricated liquid supercapacitor displays a power density of 999.8 W kg− 1 and an energy density of 19.4 Wh kg− 1 at a current density of 1 A g− 1. Undergoing 10,000 cycles at 2 A g− 1, the supercapacitor maintains nearperfect capacitance retention and coulombic efficiency close to 100%, demonstrating its excellent durability and stability for supercapacitor applications.

Porous carbon has been intensively used for microwave absorption in merits of its outstanding specific surface area and dielectric properties. This study investigates the microwave absorption capacity of saturated wood-based activated carbon (SWAC) which was used for methylene blue treatment. The results demonstrate that SWAC, subjected to high temperature calcination, exhibits excellent microwave absorption properties. The structure, composition, micro-morphology, and electromagnetic parameters of SWAC were comprehensively analyzed using various techniques. The findings reveal that after calcination, SWAC possesses a rich pore structure, optimized material impedance matching, and the introduction of N atoms from the organic substance methylene blue into the carbon lattice of SWAC, thereby providing dipole polarization loss. These properties significantly contribute to its microwave absorption performance. The optimal reflection loss of SWAC at 6 GHz reaches −50.29 dB with an effective absorption bandwidth of 2.01 GHz, achieved at a calcination temperature of 700 °C and a paraffin matrix additive amount of 25%. The one-step treatment of SWAC proves to be a competitive and cost-effective method for producing microwave absorbers, which holds significant importance for the recovery of SWAC.

Battery electrodes, essential for energy storage, possess pores that heavily influence their mechanical properties based on the level of porosity and the nature of the pores. The irregularities in pore shape, size, and distribution complicate the accurate determination of these properties. While stress-strain measurements can shed light on a material’s mechanical behavior and predict compression limits, the complex structure of the pores poses significant challenges for accurate measurements. In this research, we introduce a simulation-driven approach to derive stress-strain data that considers porosity. By calculating relative density and the rate of volume change under compression based on porosity, and applying pressure, we conducted a parametric study to identify the elastic modulus (E) in relation to the rate of volume change. This information was utilized within a material modeling equation, generating stress-strain (S-S) curves that were further analyzed to replicate the compression behavior of the electrode material. The outcomes of this study are expected to improve the prediction accuracy of mechanical properties for porous electrode materials, potentially enhancing battery performance and refining manufacturing processes.

Nonporous materials have nano-sized pores. High specific surface area and size and shape selectivity (size and shape Selectivity) are the most important features of these materials that have led to their widespread use in various industries, such as catalysts, water treatment and separation of pollutants. The development of properties and applications of these materials depends on the fabrication of nanoporous materials with optimal and controlled structures. In this paper, porous nanostructures and supermolecular chemistry are introduced in detail. Then, a number of common nanoporous materials, such as activated carbon, metal–organic frameworks and zeolites, then various types of mineral and organic nanoporous materials as well as methods of synthesis, characterization and applications of these materials will be studied in detail.

Deuterium is a crucial clean energy source required for nuclear fusion and is a future resource needed in various industries and scientific fields. However, it is not easy to enrich deuterium because the proportion of deuterium in the hydrogen mixture is scarce, at approximately 0.016%. Furthermore, the physical and chemical properties of the hydrogen mixture and deuterium are very similar. Therefore, the efficient separation of deuterium from hydrogen mixtures is often a significant challenge when using modern separation technologies. Recently, to effectively separate deuterium, studies utilizing the ‘Kinetic Quantum Sieving Effect (KQS)’ of porous materials are increasing. Therefore, in this review, two different strategies have been discussed for improving KQS efficiency for hydrogen isotope separation performance using nanoporous materials. One is the gating effect, which precisely controls the aperture locally by adjusting the temperature and pressure. The second is the breathing phenomenon, utilizing the volume change of the structure from closed system to open system. It has been reported that efficient hydrogen isotope separation is possible using these two methods, and each of these effects is described in detail in this review. In addition, a specific-isotope responsive system (e.g., 2nd breathing effect in MIL-53) has recently been discovered and is described here as well.

In this study, we developed a facile and template-free strategy for the preparation of activated porous carbon beads (APCBs) from polyacrylonitrile. The chemical activation with KOH was found to enhance the pore properties, such as specific surface area (SSA), pore volume, and pore area. The APCBs exhibited a large SSA of 1147.99 m2/g and a pore area of 131.73 m2/g. The APCB-based electrodes showed a good specific capacitance of 112 F/g at 1 A/g in a 6 M KOH electrolyte, and excellent capacitance retention of 100% at a current density of 5 A/g after 1000 cycles. Therefore, the APCBs prepared in this study can be applied as electrode materials for electric double-layer capacitors.

The porous carbons with high specific surface area and excellent electrochemical properties were prepared using three types of green needle coke as raw materials. Electrochemical performances of the porous carbons derived from different microstructure green needle coke were investigated. The XRD and Raman spectra demonstrated that the content of the ordered carbon microcrystals were decreased and the content of amorphous and cross-linked structure were increased in the porous carbons with comparison to the raw materials. The results of N2 adsorption–desorption analysis verified that the content of ordered microcrystalline structure in the raw materials evidently influence the specific surface area and pore size distribution of the porous carbons. The porous carbon with 1665 m2 g−1 specific surface area and 2.89 nm average pore size has shown that the specific capacitance was 288 F g−1 at the current density 1 A g−1. Furthermore, the capacity retention was 94.93% and the Coulombic efficiency was 92.87% after 5000 charge/discharge cycles.

Salacca peel-based porous carbon (SPPC) with high surface area (1945 m2 g−1) and large specific pore volume (1.68 cm3 g−1) was prepared by pre-carbonization and K2CO3 activation method. Based on the TGA results, it can be estimated that up to 70 wt% of sulfur-active materials could be infiltrated into the pores of SPPC to form SPPC/S composite cathode for LiS battery. The porous structure of SPPC could act as a buffer layer against volume expansion and minimize the shuttle effect due to the penetration of intermediate polysulfides during cycle tests. Optimization on sulfur loading (50, 60 and 70 wt%) in SPPCC/S composite was also investigated. It was found that the SPPC/S composites with 60 wt% of sulfur loading had the best electrochemical performances. With 60 wt% of sulfur loading, SPPC/S composite electrodes showed excellent electrochemical performances in terms of high initial specific discharge capacity of 1006 mAh g− 1 at 0.5 C and capacity retention of 71% until the 100th cycle. For both cases of low and high sulfur loading, they caused much worse electrochemical performances. Based on the experimental results, it can be concluded that porous carbons derived from the salacca peel were promising materials for sulfur loading in LiS battery.

The study presented in the article is focused on use of graphene obtained by novel microwave-enhanced chemical vapor deposition (MECVD) method as a construction material for 3D porous structures—aerogels and sponges. MECVD graphene nanoplatelets-based aerogels were obtained by mixing MECVD graphene nanoplatelets and chitosan, dissolved in 3% acetic acid followed by its freeze drying and carbonization at 800° in inert medium. Surface morphology of aerogels was characterized by SEM. MECVD graphene nanoplatelets-based aerogels are characterized by a porous structure; they are superhydrophobic and possess high sorption capacity with regard to organic liquids of different densities. Polyurethane sponges coated with MECVD graphene can serve as an alternative to aerogels. The process of their obtaining is cheaper and less complicated. They were obtained by facile “dip-coating” method, modifying its surface to increase its hydrophobicity. The resulting sponges are superhydrophobic and superoleophilic, and demonstrate high rate of sorption of organic liquids and can be easily regenerated by squeezing. In addition, they can be used as a separating material in conjunction with vacuum system for continuous and selective collection of organic liquids from the surface of water.

The stereotype of flexible MOFs(Amino-MIL-53) and carbonized porous carbon prepared from renewable resources is successfully synthesized for CO2 reduction application. The textural properties of these microporous materials are investigated, and their CO2 storage capacity and separation performance are evaluated. Owing to the combined effects of CO2-Amino interaction and its flexibility, a CO2 uptake of 2.5 mmol g−1 is observed in Amino-MIL-53 at 20 bar 298 K. In contrast, CH4 uptake in Amino-MIL-53 is very low up to 20 bar, implying potential sorbent for CO2/CH4 separation. Carbonized samples contain a small quantity of metal residues(K, Ca, Mg, S), resulting in naturally doped porous carbon. Due to the trace metal, even higher CO2 uptake of 4.7 mmol g−1 is also observed at 20 bar 298 K. Furthermore, the CH4 storage capacity is 2.9 mmol g−1 at 298 K and 20 bar. To evaluate the CO2 separation performance, the selectivity based on ideal adsorption solution theory for CO2/CH4 binary mixtures on the presented porous materials is investigated.

Porous materials play a vital role in science and technology. The ability to control their pore structures at the atomic, molecular, and nanometer scales enable interactions with atoms, ions and molecules to occur throughout the bulk of the material, for practical applications. Three-dimensional (3D) porous carbon-based materials (e.g., graphene aerogels/hydrogels, sponges and foams) made of graphene or graphene oxide-based networks have attracted considerable attention because they offer low density, high porosity, large surface area, excellent electrical conductivity and stable mechanical properties. Water pollution and associated environmental issues have become a hot topic in recent years. Rapid industrialization has led to a massive increase in the amount of wastewater that industries discharge into the environment. Water pollution is caused by oil spills, heavy metals, dyes, and organic compounds released by industry, as well as via unpredictable accidents. In addition, water pollution is also caused by radionuclides released by nuclear disasters or leakage. This review presents an overview of the state-of-the-art synthesis methodologies of 3D porous graphene materials and highlights their synthesis for environmental applications. The various synthetic methods used to prepare these 3D materials are discussed, particularly template-free self-assembly methods, and template-directed methods. Some key results are summarized, where 3D graphene materials have been used for the adsorption of dyes, heavy metals, and radioactive materials from polluted environments.

Silicon alloys are considered promising anode active materials to replace Li-ion batteries by graphite powder, because they have a relatively high capacity of up to 4200 mAh/g, and are environmentally friendly and inexpensive ECO-materials. However, its poor charge/discharge properties, induced by cracking during cycles, constitute their most serious problem as anode electrode. In order to solve these problems, Si-Ge-Al alloys with porous structure are designed as anode alloy powders, to improve cycling stability. The alloys are melt-spun to obtain the rapidly solidified ribbons, and then ball-milled to make fine powders. The powders are etched using 1 M HCl solution, which gives the powders a porous structure by removing the element Al. Subsequently, in this study, the microstructures and the characteristics of the etched powders are evaluated for application as anode materials. As a result, the etched porous powder shows better electrochemical properties than as-milled Si-Ge-Al powder.

Monolithic carbon foams with hierarchical porosity were prepared from polyurethane templates and resol precursors. Mesoporosity was achieved through the use of soft templating with surfactant Pluronic F127, and macroporosity from the polyurethane foams was retained. Conditions to obtain high porosity materials were optimized. The best materials have high specific surface areas (380 and 582 m2 g–1, respectively) and high electrical conductivity, which make them good candidates for supports in sensors. These materials showed an almost linear dependence between the potential and the pH of aqueous solutions.

In olefin/paraffin separation process, new technology such as membrane separation process has been ever demanding for both economic and environmental reasons. facilitated olefin transport membrane, containing positively charged silver nanoparticles (Ag NPs) by electron acceptor 7,7,8,8-tetracyanoquinodimethane (TCNQ) as olefin carriers dispersed in poly(vinyl pyrrolidone) (PVP), shows extremely high separation performance for propylene/propane mixtures. However, higher permeance is always demanding for practical applications. In this study, POSSs were added to PVP/Ag NPs/TCNQ membranes. Among various kinds of POSS, trisilanolisooctyl POSS showed higher permeance with a moderate selectivity. Therefore it is concluded that mesoporous POSS is an effective additive in improving the gas permeance.

단감을 재배하는 농가에서 저장성을 향상 시킬 수 있는 값싸고 쉬운 방법을 개발하기 위해 본 연구를 수행 했다. 농가 관행 LDPE 포장재 내에 동봉할 수 있는 천연소재(대나무활성숯, 왕겨숯, 겔라이트)를 선발하여 상온과 저온환경에서 가용성 고형물 함량, 경도, 식미, 부패도, 연화도의 변화를 1주일 또는 2주일 간격으로 조사 하였다. 대나무활성숯을 동봉한 LDPE 포장 방법이 단순 LDPE 포장 방법 보다 저장성 및 품질을 을 좋게 유지하였다. 대나무활성숯을 동봉한 LDPE 포장 방법은 관행 농법 농가와 유기 농법 농가 모두에서 장기 저장 시 그리고 유통 중 온도변화 시 저장성을 향상 시킬수 있는 값싸고, 손쉬운 방법으로 활용할 수 있을 것으로 판단된다.