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The carbonization of lignocellulosic biomass with ionic liquids (ILs) are considered as an advantageous approach for the preparation of carbonaceous materials. The commonly used imidazolium and pyridinium based ILs have drawbacks such as toxicity, resistance to biodegradation, high cost and viscosity. These issues can be mitigated by diluting ILs with water, although excessive water content above 1 wt% can reduce the solubility of biomass. This research aims to investigate the potential of pretreating wastepaper with a "fully green" ILs, amino acid-based IL with high water content, followed by pyrolysis without IL, in enhancing the properties of biochar. For this purpose, the paper was treated with an aqueous solution of IL cysteine nitrate ([Cys][NO 3 ]), and the IL was not involved in the pyrolysis process to prevent the formation of secondary gaseous pollutants. The findings revealed that the hemicellulose and mineral filler in the paper were eliminated during pretreatment, leading to higher carbon content but lower oxygen content. As a result, the biochar exhibited micropores of 0.42 cm3g-1 and a specific surface area of 1011.21 m2 g−1. The biochar demonstrated high adsorption capacities for Cd2+, enrofloxacin, bisphenol A, ciprofloxacin, and tetracycline, with values of 45.20 mg g−1, 49.82 mg g−1, 49.90 mg g−1, 49.88 mg g−1, and 49.65 mg g−1, respectively. The proposed mechanism for the adsorption of enrofloxacin by the biochar primarily involves physical adsorption such as pore filling and electrostatic interactions, along with chemical adsorption facilitated by graphitic nitrogen. [Display omitted] • Amino acid-based IL with high water content removed the hemicellulose and minerals. • The specific surface area was four times of that of biochar without pretreatment. • More nitrogen was retained in the biochar and provided adsorption sites. [ABSTRACT FROM AUTHOR]

Adsorption cooling and desalination systems have a distinct advantage over other systems that use low‐grade waste heat near ambient temperature. Since improving their performance, including reliability and failure prediction, is challenging, developing an efficient diagnostic system is of great practical significance. The paper introduces artificial intelligence (AI) and an automated machine learning approach (AutoML) in a real‐life application for a computational diagnostic system of existing adsorption cooling and desalination facilities. A total of 1769 simulated data points containing data indicating a failure status are applied to develop a comprehensive AI‐based Diagnostic (AID) system covering a wide range of 42 input parameters. The paper introduces a conditional monitoring system for adsorption cooling and desalination systems. The novelty of the presented study mainly consists of two aspects. First, the intelligent system predicts the health or failure states of various components in a complex three‐bed adsorption chiller installation using the extensive input data sets of 42 different operating parameters. The developed AID expert tool, based on selecting the best from 42 models generated by the DataRobot platform, was validated on the complex, existing three‐bed adsorption chiller. The AID system correctly identified healthy and failure states in various installation components. The developed expert system is very efficient (AUC = 0.988, RMSE = 0.20, LogLoss = 0.14) in predicting emergency states. The proposed method constitutes a quick and easy technique for failure prediction and represents a complementary tool compared to the other condition monitoring methods. [ABSTRACT FROM AUTHOR]

In the last decade, biochar application research has emerged as a hot topic in water treatment studies, which made biochar adsorption one of the primary wastewater treatment strategies. This paper presents a global bibliometric analysis of 2673 publications from the Web of Science database, spanning 2011–2022. For a comprehensive understanding of the research status and trends in biochar adsorption for wastewater treatment, the advanced quantitative and visual analysis tools (i.e., CiteSpace and ArcGIS) were employed. The results showed that China emerged as the leading country with the most published articles. The key research area is on the magnetic adsorption of biochar in wastewater. The articles summarized in the review demonstrated unequivocally that biochar can treat a wide range of wastewater even though the adsorption mechanisms of biochar on heavy metals, inorganic salts and organic pollutants in wastewater are not entirely consistent. The review further analyzes the factors affecting the performance of biochar in adsorbing pollutants from wastewater and the improvement measures of biochar functional characteristics, proposing the future research directions focusing on the improvement of the adsorption capacity of biochar products. The information synthesis and discussion would provide valuable insights on the historical, current, and future trends in biochar research, beneficial to solve the practical problems of water pollution and improve the quality of the environment. [ABSTRACT FROM AUTHOR]

In this paper, coal measure kaolin after flotation decarburization was made into an adsorbent by ball milling and acid modification to absorb methylene blue in water, achieving the treatment of waste with waste. The objective of this paper is to expand the application of coal measure kaolin, reduce its stock, and lower the raw material cost of adsorbents while treating wastewater containing methylene blue. The optimum milling time, acid boiling conditions, and adsorption conditions were investigated. Furthermore, the adsorption mechanism was investigated by kinetic calculation. The results show that the optimum milling time is 7 h. Relatively good acid modification conditions include a boiling temperature of 100 °C, a stirring time of 135 min, a stirring speed of 1000 r·min−1, and a concentration of hydrochloric acid of 8 mol·L−1. When 0.05 g of flotation kaolin adsorbent was used to adsorb the solution with pH 12 and a methylene blue concentration of 100 mg·L−1, the optimal adsorption conditions were a 38.05 °C adsorption temperature, a 160 r·min−1 stirring speed, and a 31.02 min stirring time. Under these optimal conditions, the adsorption quantity reached 39.92 mg·g−1. The adsorption process involves physical adsorption and spontaneous adsorption. The adsorption type is known as the quasi-second-order adsorption kinetic model. The adsorption form is heterogeneous adsorption in which a monolayer and a multi-molecular layer coexist. [ABSTRACT FROM AUTHOR]

Tetracycline's accumulation in the environment poses threats to human health and the ecological balance, necessitating efficient and rapid removal methods. Novel porous metal–organic framework (MOF) materials have garnered significant attention in academia due to their distinctive characteristics. This paper focuses on studying the adsorption and removal performance of amino-modified MIL-101(Fe) materials towards tetracycline, along with their adsorption mechanisms. The main research objectives and conclusions are as follows: (1) NH2-MIL-101(Fe) MOF materials were successfully synthesized via the solvothermal method, confirmed through various characterization techniques including XRD, FT-IR, SEM, EDS, XPS, BET, and TGA. (2) NH2-MIL-101(Fe) exhibited a 40% enhancement in tetracycline adsorption performance compared to MIL-101(Fe), primarily through chemical adsorption following pseudo-second-order kinetics. The adsorption process conformed well to Freundlich isotherm models, indicating multilayer and heterogeneous adsorption characteristics. Thermodynamic analysis revealed the adsorption process as a spontaneous endothermic reaction. (3) An increased adsorbent dosage and temperature correspondingly improved NH2-MIL-101(Fe)'s adsorption efficiency, with optimal performance observed under neutral pH conditions. These findings provide new strategies for the effective removal of tetracycline from the environment, thus holding significant implications for environmental protection. [ABSTRACT FROM AUTHOR]

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In order to achieve the purpose of efficiently removing lead and cadmium as the main heavy metals from wastewater, this paper explores the adsorption properties of cadmium ions and lead ions on biochar under different modified conditions prepared from corn stalks as raw materials and potassium phosphate as surface modifiers. Before preparing biochar (BC), the mass ratios of 1:1 and 1:2 (corn stalks to potassium phosphate) were used for pre-modification, and the oxygen-restricted pyrolysis processes of 350 °C, 550 °C and 750 °C were used for treatment. The study discussed the individual and composite adsorption effects of biochar on Pb2+ and Cd2+ under different conditions. The experimental results show that phosphorus modification has changed the physical and chemical properties of the original biochar. Among them, the biochar (2PBC550) with an impregnation ratio of 1:2 and a pyrolysis temperature of 550 °C (2PBC550) exhibits excellent adsorption properties. When the pH of the simulated wastewater is 5 and the amount of adsorbent is 30 mg·L−1, the maximum adsorption capacity of Pb2+ and Cd2+ is 145.48 mg·g−1 and 14.533 mg·g−1, respectively, which are 6.46 times and 3.67 times of the original biochar. The Pb2+ and Cd2+ adsorption data of 2PBC550 fit well with the quasi-secondary dynamics and Langmuir isothermal models, indicating that the adsorption process is controlled by single-layer chemical adsorption. In the composite metal system of Pb2+ and Cd2+, 2PBC550 exhibits a stronger affinity for Pb2+ than Cd2+. Through the analysis of characterization methods such as SEM, FTIR, XRD and XPS, it is proved that the adsorption of Pb2+ and Cd2+ by 2PBC550 is due to precipitation, complexation and π electron interaction. Therefore, 2PBC550 shows great application potential in the repair of wastewater containing Pb2+ or Cd2+. [ABSTRACT FROM AUTHOR]

The enhanced coalbed methane recovery using CO2 injection (CO2-ECBM) is widely proposed as a way of achieving the energy transition and reducing atmospheric CO2 in areas such as the Lorrain basin in France, where heavy industry is responsible for huge CO2 emissions and coal mines have been closed for more than a decade. This paper deals with the feasibility of extracting methane from the Lorraine basin using CO2-ECBM by comparing data from sorption isotherms, thermogravimetric analyses and breakthrough curves for two coal samples. One is bituminous (Box 18), from Folschviller (France) and is compared with another sub-bituminous (TH01) from La Houve (France), which is used as a reference because it was identified as a good candidate for CO2-ECBM in a previous research program. The quantities of adsorbed gases (CO2/CH4) obtained by sorption isotherms, thermogravimetry and CO2 breakthrough curves showed that Box 18 adsorbs more CO2 and CH4 than TH01 due to its higher porosity and good affinity for gases (CO2/CH4). Tόth model fits the experimental CH4 and CO2 adsorption isotherms better, reflecting the fact that the adsorption surface of the coals studied is heterogeneous. Adsorption enthalpies obtained by calorimetry indicated physisorption for gas-coal interactions, with higher values for CO2 than for CH4. Thermogravimetric analyses and breakthrough curves carried out at up to 50% relative humidity showed that the adsorption capacity of CO2 decreases with increasing temperature and the presence of water, respectively. The compilation of these experimental data explained the adsorption process of the studied coals and revealed their advantages for CO2-ECBM. Highlights: The Folschviller coal from Lorrain basin (France) meets the main criteria to be a good candidate for CO2-ECBM due to his porosity network, adsorption capacity and affinity for gases (CO2/CH4). The binding energy between the gas and the coal samples is low corresponding to physical adsorption; however, chemical adsorption of CO2 was detected by thermogravimetry at atmospheric pressure. Calorimetry and sorption isotherms modelling showed that the adsorption surface of coal is heterogeneous with a progressive filling of the high energy sites towards the lower energy sites. The breakthrough curves and thermogravimetry carried out at atmospheric pressure showed respectively that water and temperature reduce the CO2 adsorption capacity of coals. [ABSTRACT FROM AUTHOR]

The recovery of valuable gold from wastewater is of great interest because of the widespread use of the precious metal in various fields and the pollution generated by gold-containing wastes in water. In this paper, a water-insoluble cross-linked adsorbent material (TE) based on cyanuric chloride (TCT) and ethylenediamine (EDA) was designed and used for the adsorption of Au(III) from wastewater. It was found that TE showed extremely high selectivity (D = 49,213.46) and adsorption capacity (256.19 mg/g) for Au(III) under acidic conditions. The adsorption rate remained above 90% eVen after five adsorption–desorption cycles. The adsorption process followed the pseudo-first-order kinetic model and the Freundlich isotherm model, suggesting that physical adsorption with a multilayer molecular overlay dominates. Meanwhile, the adsorption mechanism was obtained by DFT calculation and XPS analysis, and the adsorption mechanism was mainly the electrostatic interaction and electron transfer between the protonated N atoms in the adsorbent (TE) and AuCl4−, which resulted in the redox reaction. The whole adsorption process was the result of the simultaneous action of physical and chemical adsorption. In conclusion, the adsorbent material TE shows great potential for gold adsorption and recovery. [ABSTRACT FROM AUTHOR]

This paper proposes a new, highly effective fluorescence test for Cr(VI) detection. This method utilizes a hydrogel composed of hydroxyethyl cellulose (HEC), nitrogen-doped carbon quantum dots (N–CQDs), and poly(co-acrylamido-2-methyl-1-propane sulfonic acid) (AMPS). The N–CQDs were successfully synthesized using a simple microwave method, and then conjugated with HEC and AMPS. The higher adsorption (99.41%) and higher reduction rate in H1 likely stems from both the presence of N–CQDs (absent in HB) and their increased free functional groups (compared to H2/H3, where N–CQDs block them). This facilitates the release (desorption) of Cr(VI) from the hydrogels, making it more available for reduction to the less toxic Cr(III). The fluorescent brightness of the HEC-N–CQDs-g-poly(AMPS) hydrogel increases gradually when Cr(VI) is added in amounts ranging from 15 to 120 mg/L. The fluorescent enhancement of the HEC-N–CQDs-g-poly(AMPS) hydrogel appeared to exhibit a good linear relationship with the 15–120 mg of the Cr(VI) concentration, with a detection limit of 0.0053 mg/L, which is lower than the standard value published by WHO. Our study found that the HEC-N–CQDs-g-poly(AMPS) hydrogel served effectively as a fluorescent probe for Cr(VI) detection in aqueous solutions, demonstrating high sensitivity. [ABSTRACT FROM AUTHOR]

This document discusses the molecular structure of coal and its impact on methane adsorption. The complex composition of coal, including organic and inorganic matter, affects its adsorption capacity. Various experimental techniques, such as spectroscopy and microscopy, can be used to study the chemical structure of coal. The document also highlights several research papers that explore the pore structure and gas content of coal, providing insights for coalbed methane production and exploration. The authors of these papers are from China, reflecting the country's focus on coal research due to its abundant reserves. [Extracted from the article]

More than 70% of the potash fertilizer globally is produced by the froth flotation process, in which 4-dodecylmorpholine (DMP) serves as a reverse flotation agent. As the potash fertilizer production rapidly rises, the increased DMP levels in discharged brine pose a threat to the production of high-value chemicals. In this paper, composite particles of basic magnesium sulfate@TiO2 (BMS@TiO2) were prepared using a simple and mild loading method. These particles were utilized for the adsorption and photocatalytic degradation of DMP in brine. Compared with normal powdered materials, the granular BMS@TiO2 in this study can be easily separated from liquid, and the degradation intermediates will not enter the brine without causing secondary pollution. BMS@TiO2 consists of 5·1·7 phase (5Mg(OH)2·MgSO4·7H2O) whisker clusters embedding 2.3% TiO2. The adsorption equilibrium of DMP on BMS@TiO2 particles was achieved through hydrogen bonding and pore interception with the adsorption capacity of approximately 5 mg g−1 after 6 h. The photodegradation efficiency of DMP adsorbed on BMS@TiO2 reached about 92% within 16 h, which is compared with that of pure TiO2 nanoparticles. Additionally, excellent stability and recyclability of BMS@TiO2 were also observed in five cycle tests of adsorption and photocatalytic degradation of DMP, and the possible photocatalytic degradation pathways and mechanism of DMP are proposed following molecular electrostatic potential analysis. This work provides a sustainable and environmentally friendly approach for eliminating organic micropollutants from water environments. [ABSTRACT FROM AUTHOR]

In this paper, we report the synthesis of a multi-template molecularly imprinted polymer (MIP) to target and extract naproxen, ibuprofen, diclofenac, emtricitabine, tenofovir disoproxil, and efavirenz from wastewater bodies. A bulk polymerization procedure was used to synthesize the MIP and non-imprinted polymer (NIP). The specific recognition sites for each target were obtained through the removal of the imprinted targeted compounds. The interaction of antiretroviral drugs (ARVs) and non-steroidal anti-inflammatory drugs (NSAIDs) compounds with the MIP was studied under various conditions such as pH, mass, concentration, and time factors. The results demonstrated the optimum conditions were 55 mg of MIP, pH 7.0, a concentration of 5 mg L−1, and a contact time of 10 min. For every compound studied, the extraction efficiencies for ARVs and NSAIDs in aqueous solutions was >96%. The adsorption capacity for the MIP was >0.91 mg·g−1. Adsorption obeys a second-order rate, and the Freundlich model explains the adsorption isotherm data. This study demonstrated that the synthesized multi-template MIP has huge potential to be employed for the removal of ARVs and NSAIDs from the environment as well as in drug purification or recovery processes. [ABSTRACT FROM AUTHOR]

In recent years, due to the rapid growth of mankind's demand for energy, harmful gases (SOx) produced by the combustion of sulfur-containing compounds in fuel oil have caused serious problems to the ecological environment and human health. Therefore, in order to solve this hidden danger from the source, countries around the world have created increasingly strict standards for the sulfur content in fuel. Adsorption desulfurization technology has attracted wide attention due to its advantages of energy saving and low operating cost. This paper reviewed the latest research progress on various porous adsorption materials. The future challenges and research directions of adsorption materials to meet the needs of clean fuels are proposed. [ABSTRACT FROM AUTHOR]

In recent years, atmospheric composite pollution has become increasingly serious, and accelerating VOC governance has become the focus of and difficulty in atmospheric governance. Volatile organic compounds (VOCs) come from a wide range of sources, and industrial sources are the main source of anthropogenic VOC emissions in China. Chemicals, oil refining, and solvents are three typical VOC-emitting industries, and their control is an important part of accelerating and optimizing VOC governance. It can be controlled by source control, process control, and pipe end treatment; among these, pipe end treatment is divided into recovery technology and destruction technology. In pipeline end treatment, with the key materials of adsorption, absorption, catalytic oxidation, and catalytic combustion, the research and development of adsorbents, absorbents and catalysts has become a hot spot in recent years. This paper summarizes the chemical materials used in typical VOC pipe end-treatment technology (including adsorbents used in the adsorption method, absorbents used in the adsorption method, and catalysts used in the catalytic oxidation and catalytic combustion methods), summarizes the advantages and disadvantages of various materials and their application range, and looks forward to the direction of future developments. [ABSTRACT FROM AUTHOR]

In order to explore a medium material for the efficient treatment of Pb(II) pollutants in groundwater, in this paper, mudstone is selected as the medium material, and the morphological structure of the mudstone is characterizes via X-ray diffraction (XRD), scanning electron microscopy (SEM), and Brunauer–Emmett–Teller (BET) analyses to study the feasibility of the mudstone adsorbing Pb(II) ions. Then, static adsorption experiments are carried out to investigate the removal effect of mudstone on Pb(II) in aqueous solutions under different conditions and to determine the optimal adsorption conditions. Finally, the results are fitted and analyzed using a thermodynamic model to explore the adsorption mechanism of the mudstone. The main results of this study are as follows. The main mineral composition of the mudstone used in the experiments includes CaCO3, SiO2, CaAl2O4·10H2O, and CaFe4O7. The specific surface area of the mudstone is as high as 23.027 m2·g−1, the pore size is 9.145 nm, and its surface structure is rough, with pores and fissures developed. The pore space and adsorption capacity of the mudstone were enhanced. When 1 g·L−1 of mudstone was added, the pH value of the solution was 6, the reaction time was 60 min, and the initial concentration of Pb(II) was 30 mg·L−1. The removal efficiency of Pb reached 84.5%, and the adsorption amount was 25.352 mg·g−1. For the removal of Pb(II) from the aqueous solution by the mudstone under different concentrations of Pb(II), the reaction was in accordance with the Langmuir adsorption isotherm model, and the maximum adsorption amount reached 54.975 mg·g−1. The relationship between the removal of Pb(II) and the reaction time was in accordance with the pseudo-second-order rate model. The results of this study suggest that mudstone can be used for the removal of Pb(II) from aqueous media. [ABSTRACT FROM AUTHOR]

Underwater unmanned robots are an essential tool for human underwater exploration and detection and are widely employed in a variety of underwater operational settings. One of the hottest issues in this field is applying bionic notions to the creation of underwater unmanned robots by simulating fish swimming or cephalopod crawling. Using the tentacle suction cup adsorption technique during octopus' predation as a model, underwater magnetic adsorption robots with the opening and closing claws were studied in this paper. First, the robot's general structural design is presented. The claw mechanism is demonstrated by mimicking the octopus's tentacle action during feeding, which primarily consists of an opening and closing claw that replicates the octopus's tentacle and a magnetic adsorption unit that replicates the octopus's suction cup adsorption. Then, the Kriging response surface optimization method is used to optimize the design of the claw mechanism to obtain excellent mechanical properties, and simulation software is used to verify. Finally, a robot prototype was built and its pool tests were conducted, with some experimental results presented. The experimental results show that after the robot reaches the predetermined position through pneumatic ejection and secondary propulsion launch, it can quickly open its claws within 0.11 s and apply 462.42 N adsorption force to complete the adsorption of the target. [ABSTRACT FROM AUTHOR]

Glyceryl monostearate (GMS) was used as an organic friction modifier (OFM) and added to the base oil (PAO10, polyα-olefin) in this study. The film thickness and friction coefficient of the base oil added with GMS (PAO10G) under different slider inclinations and loads were investigated experimentally by using a slider-on-disc contact lubricant film measurement system, and the effect of the adsorption of GMS on the friction behavior of lubricant was studied. Contact angle hysteresis (CAH) was used to evaluate the wettability of the solid–liquid interface, and its correlation with the coefficient of friction was analyzed. The results show that CAH is in good agreement with the wettability of the solid–liquid interface. Compared with the base oil, the wettability of POA10G is weak, which can effectively reduce the coefficient of friction. However, different from the classical lubrication theory, the film thickness of PAO10G is higher than that of PAO10; this unusual phenomenon is preliminarily explained by the interface slippage in this paper. [ABSTRACT FROM AUTHOR]

In this paper, the physical adsorption of volatile organic compounds (VOCs) such as methyl chloride (CH3Cl), carbon disulfide (CS2), dimethyl sulfide (C2H6S), and benzene (C6H6) by three models of activated carbon (without a functional group, with a pyridine-containing functional group, and with a pyrrole-containing functional group) was simulated. The surface electrostatic potential (ESP), physical adsorption energy, and non-covalent interaction between activated carbon and VOC molecules were analyzed based on the density functional theory (DFT). The effect mechanism of nitrogen-containing functional groups on VOC adsorption by activated carbon was determined. Our simulations showed that nitrogen-containing functional groups can change the surface ESP and polarity of activated carbon. The pyrrole functional group is conducive to CH3Cl and CS2 adsorption on the activated carbon plane, while the pyridine functional group is relatively small or even unfavorable for CH3Cl and CS2 adsorption on the activated carbon plane. The promotional effect of the pyrrole functional group on the adsorption of C2H6S is more significant than that of the pyridine functional group. The adsorption of C6H6 on activated carbon occurs through parallel-displaced π–π stacking interactions, in which functional groups have little influence on it. The adsorption energy of VOCs on the activated carbon plane is higher than that at the edge, so VOCs are more likely to be adsorbed on the activated carbon plane. [ABSTRACT FROM AUTHOR]

Oil-immersed transformers play a pivotal role owing to their environmentally friendly characteristics, compact footprint, and cost-effectiveness. Ensuring the online monitoring of oil-immersed transformers is a fundamental measure to ensure the secure and stable operation of modern power systems. In this paper, metal particle cluster-doped SnS is firstly used in the adsorption and sensing of decomposition components (CO, C2H2) under fault conditions in oil-immersed transformers. The study comprehensively analyzed band structure, differential charge density, density of states, and molecular orbital theory to unveil the adsorption and sensing mechanisms of target gases. The findings suggest that the modification of metal particle clusters can enhance the surface electronic properties of single-layer SnS. In the regions of metal particle clusters and the gas–surface reaction area, electronic activity is significantly heightened, primarily attributed to the contribution of d-orbital electrons of the metal cluster structures. The modified SnS exhibits adsorption capacity in the following order: Ru3-SnS > Mo3-SnS > Au3-SnS. Additionally, the modified material demonstrates increased competitiveness for C2H2, with adsorption types falling under physical chemistry adsorption. Different metal elements exert diverse effects on the electronic distribution of the entire system, providing a theoretical foundation for the preparation of corresponding sensors. The findings in this work offer numerical insights for the further preparation and development of SnS nanosensors, concurrently shedding light on the online monitoring of faults in oil-immersed transformers. [ABSTRACT FROM AUTHOR]

The paper presents the results of experimental and model studies of the pressure swing adsorption (PSA) process in a column with a zeolite 13X bed with a height of 0.5 m. The gas mixture consisted of CO2 (10–20%), N2, and H2O (RH 50%) in different ratios. As a result of the column tests, concentration, and temperature evolutions were obtained for each of the adsorption and desorption stages, which were used to determine the breakthrough and bed saturation times and other parameters important for the analysis of the column operation. A mathematical model of the PSA process for the separation of CO2 from the gas mixture was developed. The system of second-order partial differential equations was solved using Matlab software. The research focuses on adsorptive CO2 capture and shows the influence of water vapor and operational parameters on the quality of model validation. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) represent the largest class of materials among crystalline porous materials ever developed, and have attracted attention as core materials for separation technology. Their extremely uniform pore aperture and nearly unlimited structural and chemical characteristics have attracted great interest and promise for applying MOFs to adsorptive and membrane-based separations. This paper reviews the recent research into and development of MOF membranes for gas separation. Strategies for polycrystalline membranes and mixed-matrix membranes are discussed, with a focus on separation systems involving hydrocarbon separation, CO2 capture, and H2 purification. Challenges to and opportunities for the industrial deployment of MOF membranes are also discussed, providing guidance for the design and fabrication of future high-performance membranes. The contributions of the underlying mechanism to separation performance and adopted strategies and membrane-processing technologies for breaking the selectivity/permeability trade-off are discussed. [ABSTRACT FROM AUTHOR]

The paper investigates the solar photodegradation of Methylene Blue dye using copper oxide (CuO) thin films synthesized by the Successive Ionic Layer Adsorption and Reaction (SILAR) method. The structural, morphological, and optical characteristics of the CuO thin films have been investigated by employing a variety of methods, such as Fourier transform Infrared (FTIR) spectroscopy, UV-Vis spectroscopy, Scanning electron microscopy (SEM), and X-ray diffraction (XRD). The outcomes showed that CuO thin films with excellent surface shape and a highly crystalline nature had been successfully deposited. Methylene Blue was subjected to solar radiation during its photodegradation process, and the outcomes showed a significant decrease in the dye's concentration over time. To maximize the photodegradation process, the effects of other experimental factors were also assessed, such as the starting concentration of MB, the quantity of CuO thin film, the number of SILAR cycles and the pH of the solution. Good photocatalytic activity is demonstrated by CuO thin films produced using the SILAR approach in the solar photodegradation of methylene blue. The development of affordable and ecologically friendly wastewater treatment technology that can use sun energy to break down persistent organic contaminants is affected by these findings. [ABSTRACT FROM AUTHOR]

The direct discharge of rare earth wastewater causes the waste of resources and heavy metal pollution. This paper compared the adsorption behaviors of lanthanide ions on bentonite under sulfate and nitrate systems by examining the factors affecting the adsorption, such as adsorption time, pH, background electrolyte concentration, and initial rare earth ion concentration. It was shown that the sulfate system was more favorable for the adsorption of rare earth ions on the bentonite surface. The maximum adsorption capacity in the sulfate system was about 1.7 times that in the nitrate system. In contrast, the adsorption under the nitrate system was more sensitive to the changes in pH and background electrolyte concentration. The adsorption processes under both systems are spontaneous physical adsorption processes (ΔGθ are from −27.64 to −31.48 kJ/mol), and both are endothermic (ΔHθ are 10.38 kJ/mol for the nitrate and 7.53 kJ/mol for the sulfate) and entropy-increasing (ΔSθ are 61.54 J/mol for the nitrate and 76.24 J∙mol−1 for the sulfate) processes. This study helps to provide information about the optimizing process parameters for the adsorption treatment of rare earth wastewater using bentonite. [ABSTRACT FROM AUTHOR]

The advanced Gas Insulated Switchgear/Gas Insulated Lines (GIS/GIL) transmission equipment serves as an essential physical infrastructure for establishing a new energy power system. An analysis spanning nearly a decade on faults arising from extra/ultra-high voltage discharges reveals that over 60% of such faults are attributed to the discharge of metal particles and dust. While existing technical means, such as ultra-high frequency and ultrasonic sensing, exhibit effectiveness in online monitoring of particles larger than sub-millimeter dimensions, the inherent randomness and elusive nature of micron-nano dust pose challenges for effective characterization through current technology. This elusive micron-nano dust, likely concealed as a latent threat, necessitates special attention due to its potential as a "safety killer". To address the challenges associated with detecting micron-nano dust and comprehending its intricate mechanisms, this paper introduces a micron-nano dust adsorption experimental platform tailored for observation and practical application in GIS/GIL operations. The findings highlight that micron-nano dust's adsorption state in the electric field predominantly involves agglomerative adsorption along the insulator surface and diffusive adsorption along the direction of the ground electrode. The pivotal factors influencing dust movement include the micron-nano dust's initial position, mass, material composition, and applied voltage. Further elucidation emphasizes the potential of micron-nano dust as a concealed safety hazard. The study reveals specific physical phenomena during the adsorption process. Agglomerative adsorption results in micron-nano dust speckles forming on the epoxy resin insulator's surface. With increasing voltage, these speckles undergo an "explosion", forming an annular dust halo with deepening contours. This phenomenon, distinct from the initial adsorption, is considered a contributing factor to flashovers along the insulator's surface. The physical mechanism behind flashovers triggered by micron-nano dust is uncovered, highlighting the formation of a localized short circuit area and intense electric field distortion constituted by dust speckles. These findings establish a theoretical foundation and technical support for enhancing the safe operational performance of AC and DC transmission pipelines' insulation. [ABSTRACT FROM AUTHOR]

The purpose of this manuscript is to present a review of laboratory experiments (including methodology and results) that use biochar, a specific carbon obtained by a pyrolysis process from different feedstocks, as an alternative material for heavy metal adsorption from groundwater. In recent years, many studies have been conducted regarding the application of innovative materials to water decontamination to develop a more sustainable approach to remediation processes. The use of biochar for groundwater remediation has particularly attracted the interest of researchers because it permits the reuse of materials that would be otherwise disposed of, in accordance with circular economy, and reduces the generation of greenhouse gases if compared to the use of virgin materials. A review of the different approaches and results reported in the current literature could be useful because when applying remediation technologies at the field scale, a preliminary phase in which the suitability of the adsorbent is evaluated at the lab scale is often necessary. This paper is therefore organised with a short description of the involved metals and of the biochar production and composition. A comprehensive analysis of the current knowledge related to the use of biochar in groundwater remediation at the laboratory scale to obtain the characteristic parameters of the process that are necessary for the upscaling of the technology at the field scale is also presented. An overview of the results achieved using different experimental conditions, such as the chemical properties and dosage of biochar as well as heavy metal concentrations with their different values of pH, is reported. At the end, numerical studies useful for the interpretation of the experiment results are introduced. [ABSTRACT FROM AUTHOR]

The issue of cigarette butts is an environmental crisis that has affected the world. Despite their small size, CBs are one of the most common types of solid waste found in public places, particularly in coastal areas. The aim of this study was to investigate the adsorption behavior of microfibers obtained from cigarette butts on tetracycline before and after aging. 1 g of CBs was added to 50 mL of distilled water and stirred at 220 rpm for 2 h, then filtered through Whatman 0.45 µm filter paper, and the resulting MFs were dried at 60 °C for 24 h. To simulate aging, the MFs were subjected to an ultrasonic treatment at a frequency of 80 Hz and a power of 70 W for 4 h. The adsorption behavior of aged and fresh MFs was investigated using solutions containing TTC in the range of 5–20 mg/L. This study showed that ultrasonically aged MFs had a greater tendency to adsorb TTC than fresh MFs due to an increased surface area and changes in surface chemistry. It can be concluded that as the age of MFs increases, they adsorb more concentration of pollutants. This can lead to increased contamination of MFs in the presence of contaminants. [ABSTRACT FROM AUTHOR]

2-ethylhexanol, an oxo alcohol competitively priced on the global market, has not been explored intensively as a raw material for surfactants, due to its weak hydrophobic character. However, its sequenced propoxylation and ethoxylation yield an innovative amphiphilic structure, which exhibits unique interfacial activity. The paper presents the differences in the fractional composition of innovative surfactants derived from 2-EH alcohol prepared using alkali and dimetalcyanide catalysts, as well as examples of excellent adsorption and interfacial properties of the latter. The adsorption behavior of the synthesized compounds was explored using equilibrium surface tension (the du Noüy ring method), dynamic surface tension (the maximum gas bubble pressure method) and static/dynamic contact angle (the sessile drop method). The results from the adsorption tests conducted at the air/aqueous surfactant solution interface underwent comprehensive qualitative and quantitative analyses. Moreover, based on the experimentally obtained dynamic surface tension isotherms and the developed algorithm, the diffusion coefficients for these preparations were estimated, and it was shown that the diffusivity of these surfactants is higher compared to the commercial formulations. The study's outcomes in the testing of wettability indicate that new synthesized nonionic and anionic surfactants constitute an interesting group of amphiphiles with a wide application potential as effective wetting agents, especially in relation to the polymer surface. It should therefore be emphasized that the innovative surfactants described in this article, derived from 2-EH alcohol and prepared using dimetalcyanide catalysts, can successfully compete with conventional preparations such as ABS (Dodecylbenzenesulfonic Acid) or AES (Alcohol Ethoxysulphate) acid salts. [ABSTRACT FROM AUTHOR]

Elevated concentrations of heavy metals in natural waters can cause significant ecological problems. It is therefore essential to ensure their removal from any water discharged into the environment immediately, especially in case of an accident, where there is a risk of releasing large quantities or high concentrations. The aim of this paper is to test a newly developed adsorbent for the removal of heavy metals from aqueous solutions—in particular, it is very fast adsorption, and thus efficiency, during clean-ups. The alkali-activated foamed zeolite adsorbent was laboratory-prepared and -tested in both batch and flow-through arrangements on single and multi-component solutions and compared with natural zeolite. The experimental setup for batch adsorption consisted of a set of samples and solutions containing iron, cobalt, manganese, zinc and nickel. The samples were put on a horizontal shaker with a 500 mg adsorbent loading in a 50 mL solution. The column adsorption experimental setup consisted of a glass column with an inside diameter of 15 mm and a bed length of 165 mm. A measured amount of each adsorbent was added to the column to achieve a filter fixed-bed height of 160 mm. The high efficiency of the tested adsorbent on various heavy metals was confirmed. The adsorbent has a high potential for use in decontamination processes, water protection and landscape revitalization. Due to its rapid precipitation and subsequent fixation of metal cations in the form of insoluble oxide or hydroxide, it can be used as an emergency adsorbent, the great advantage of which is its low production cost and natural origin. [ABSTRACT FROM AUTHOR]

Featured Application: This study aimed to synthesize a novel biomass-based, chemically activated carbon from Pinus radiata sawdust and to investigate its effectiveness in the removal of wood dyes from aqueous solutions in a fixed-bed column. In this paper, an activated carbon obtained from Pinus radiata sawdust is applied to remove blue, red, and black wood dyes from aqueous solutions in a fixed-bed column. The flow rate (7.7–30.8 mL min−1), initial dye concentration (25–500 mg L−1), and bed height (2–4 cm) highly influence the breakthrough-curves' features. The results indicate that the adsorption capacity increased by decreasing the flow rate and increasing the initial dye concentration, except for the black dye, and increasing bed height, except for the red dye. In addition, the breakthrough time changed by modifying the studied variables. The curves became steeper as the flow rate increased and as the bed height decreased. Also, by increasing the inlet dye concentration, the breakthrough time decreased significantly, and sharper breakthrough curves were obtained. The activated carbon with a surface area of 2826 m2 g−1 led to high values of the adsorption capacity between 150 and 1300 mg g−1. The Yoon–Nelson and Thomas models were the ones that best described the adsorption data. The activated carbon saturated with black dye could be used in three successive cycles after regeneration with H2O2. [ABSTRACT FROM AUTHOR]

Activated carbon fibers (ACFs) derived from various polymeric fibers with the characteristics of a high specific surface area, developed pore structure, and good flexibility are promising for the new generation of chemical protection clothing. In this paper, a polyacrylonitrile-based ACF felt was prepared via the process of liquid phase pre-oxidation, along with a one-step carbonization and chemical activation method. The obtained ACF felt exhibited a large specific surface area of 2219.48 m2/g and pore volume of 1.168 cm3/g, as well as abundant polar groups on the surface. Owing to the developed pore structure and elaborated surface chemical property, the ACF felt possessed an intriguing adsorption performance for a chemical warfare agent simulant dipropyl sulfide (DPS), with the highest adsorption capacity being 202.38 mg/g. The effects of the initial concentration of DPS and temperature on the adsorption performance of ACF felt were investigated. Meanwhile, a plausible adsorption mechanism was proposed based on the kinetic analysis and fitting of different adsorption isotherm models. The results demonstrated that the adsorption process of DPS onto ACF felt could be well fitted with a pseudo-second-order equation, indicating a synergistic effect of chemical adsorption and physical adsorption. We anticipate that this work could be helpful to the design and development of advanced ACF felts for the application of breathable chemical protection clothing. [ABSTRACT FROM AUTHOR]

The production of cobalt oxide nanoparticles and their use in the adsorption of methylene blue (MB) from solution is described in the paper. The X-ray diffraction patterns show that the synthesized cobalt oxide nanoparticles have a crystalline cubic structure. The study of the adsorption of methylene blue onto the cobalt oxide nanoparticles involved determining the contact time and initial concentration of the adsorption of MB on the adsorbent. The kinetics of adsorption were analyzed using two kinetic models (pseudo-first order and pseudo-second order), and the pseudo-second-order model was found to be the most appropriate for describing the behavior of the adsorption. This study indicates that the MLTS (monolayer with the same number of molecules per site) model is the most suitable model for describing methylene blue/cobalt oxide systems, and the parameter values help to further understand the adsorption process with the steric parameters. Indicating that methylene blue is horizontally adsorbed onto the surface of the cobalt oxide, which is bonded to two different receptor sites. Regarding the temperature effect, it was found that the adsorption capacity increased, with the experimental value ranging from 313.7 to 405.3 mg g−1, while the MLTS predicted 313.32 and 408.16 mg g−1. From the thermodynamic functions, high entropy was found around 280 mg L−1 concentration. For all concentrations and temperatures examined, the Gibbs free energy and enthalpy of adsorption were found to be negative and positive, respectively, suggesting that the system is spontaneous and endothermic. According to this study's findings, methylene blue adsorption onto cobalt oxide nanoparticles happens via the creation of a monolayer, in which the same amount of molecules are adsorbed at two distinct locations. The findings shed light on the methylene blue adsorption process onto cobalt oxide nanoparticles, which have a variety of uses, including the remediation of wastewater. [ABSTRACT FROM AUTHOR]

Sustainable development policy focuses on reducing the carbon footprint generated by the global industry and energy sector. Replacing conventional energy sources with environmentally friendly ones requires advanced research to increase energy efficiency and reduce the instability and intermittence of renewable sources. Moreover, adsorption chillers are an opportunity to introduce net-zero emission technologies to the refrigeration, air-conditioning, and desalination industries. Adsorption devices could be popularized if a method of effective heat transfer in the volume of the adsorption bed is developed. The innovative concept of introducing fluidized beds into the adsorption system can achieve the most promising results in improving energy efficiency. To confirm the adopted assumption, heat transfer coefficient calculations for the packed and fluidized bed were carried out in this paper based on experimental tests and literature data. The empirical research aims to extend the fundamental knowledge in the implementation of fluidization under low-pressure conditions, characteristic of the adsorption systems' working cycle. Experiments were conducted on a unique test stand equipped with the Intensified Heat Transfer Adsorption Bed (IHTAB) reactor prototype. Five adsorption bed samples were analyzed. The reference sample consisted only of silica gel, and the subsequent ones contained aluminum or carbon nanotubes with 5 and 10% additions. In the case of samples with admixtures, the fluidized state increased the heat transfer coefficient on average from approx. 36.9 W/m2 K to approx. 245.4 W/m2 K. [ABSTRACT FROM AUTHOR]

The presence of heavy metals in water bodies can cause major problems for human, plant, and animal life. Excessive amounts or over the prescribed limits of heavy metals in water bodies usually contaminates the water, this type of water is called polluted water and this whole process is known as water pollution. Regular consumption of heavy metal-contaminated water above prescribed limits can cause various diseases and sometimes even lead to death. Heavy metals like chromium, arsenic, lead, mercury etc. are more toxic and are easily found in water bodies due to anthropogenic and natural activities. The presence of these heavy metals in water even in tiny concentrations is dangerous to human and animal health. Due to its highly toxic nature, it is paramount to remove these pollutants from water bodies before human use. Adsorption is the best technique to remove these pollutants from wastewater based on cost, efficiency, and feasibility. For the adsorption process, a variety of adsorbent materials have been synthesized by researchers in the past few decades, and yet it remains a challenge for researchers and scientists to synthesize a cost-effective and highly efficient adsorbent. In this prospect, water treatment by adsorption process, nano-composites are emerging materials that show excellent adsorption characteristics due to their outstanding material properties, manageable and low-cost production, and excellent adsorption capacity for chromium adsorption from wastewater. The various nanocomposite adsorbent material prepared by different types of nanoparticles that are supported or embedded on biomass/biochar/graphene/polymer/etc. and used for chromium adsorption have been incorporated. The physio-chemical and structural characteristics of nanocomposites are covered in this review paper. Furthermore, the impact of various adsorption conditions, together with their benefits and drawbacks, on the effectiveness of water treatment are discussed. This thorough review concludes with a summary and some ideas about novel strategies and difficulties in the investigation of advanced and hybrid nanocomposite materials used to remove Cr(VI) from wastewater. [ABSTRACT FROM AUTHOR]

Adsorption heat storage holds great promise for solar energy applications. The development of new adsorbent materials is currently the research focus in this area. The present work designs several activated carbon models with different functional groups, including -OH, -NH2, -COOH, and -SO3H, and explores the influence of functional groups' categories and numbers on the water adsorption capacity of the activated carbon using the GCMC method. The adsorption mechanism between functional groups and water molecules is analyzed using density functional theory. The results show that the functional groups could significantly improve the water adsorption capacity of activated carbon due to the hydrogen bond between functional groups and water molecules. In the scope of this paper, under low pressure, the activated carbon with -SO3H exhibits the best adsorption capacity, followed by the activated carbon with -COOH. Under low and medium pressure, increasing the number of -SO3H functional groups could increase the water adsorption capacity; however, when the pressure is high, increasing the functional group numbers might decrease the water adsorption capacity. As the temperature increases, the water adsorption capacity of activated carbons decreases, and the activated carbon with -SO3H is proven to have excellent application prospects in heat energy storage. [ABSTRACT FROM AUTHOR]

The research work is devoted to the kinetics of adsorption. Needless to say that physical adsorption is of great interest in heat industry according to the number of research papers published in the area annually. The working pair of carbon dioxide and consolidated tablet of AC was considered. The mathematical model built for a cylindrical coordinate system, so the computational domain is a rectangle corresponding to the radial section of the tablet. The rate of adsorption implemented using the LDF (linear driving force) model. The temperature map was constructed for analyzing the behavior of the temperature field. Curves of instantaneous uptake and simulated average temperature are obtained. Simulation results are compared with experimental data and shows good agreement. The study also presents findings of a grid sensitivity analysis. The developed solver is the subject to further expansion to consider more quantities, such as change in porosity, volatile gas concentration, etc. [ABSTRACT FROM AUTHOR]

A series of morpholine salt volatile corrosion inhibitors (VCIs) were synthesized via solid-phase chemical reactions. The corrosion inhibition performance was assessed using evaporation weight loss, VCI capability, and corrosion weight loss tests. The corrosion inhibition mechanisms of the morpholine salt VCIs for carbon steel in atmospheric conditions were explored through electrochemical testing under thin film electrolytes, X-ray photoelectron spectroscopy (XPS), and computational simulations. Morpholine carbonate exhibited higher volatility. Corrosion weight loss tests showed an >85% reduction for steel treated with morpholine benzoate or morpholine carbonate. The inhibitors' inhibition mechanism, elucidated through X-ray photoelectron spectroscopy (XPS) and computational simulations, revealed that morpholine carbonate and benzoate form protective layers via physical and chemical adsorption on the steel surface, coordinating with iron atoms through nitrogen and oxygen atoms. Quantum chemical calculations demonstrated that morpholine carbonate had stronger adsorption energy and electron transfer capabilities, indicating superior corrosion inhibition performance over morpholine benzoate. [ABSTRACT FROM AUTHOR]

In order to inhibit the corrosion of ADC12 aluminum alloy caused oxalic acid in engine coolant, corrosion inhibitor technology is usually used because of its simple operation, low cost, no impact on metal heat dissipation, and effectively suppressing metal corrosion at a lower concentration. In this paper, the corrosion inhibition, long-term and adsorption mechanisms of humic acid (HA) on ADC12 aluminum alloy were studied using electrochemical testing, surface analysis techniques, and theoretical calculations. The results showed that HA was a mixed corrosion inhibitor that followed the Langmuir adsorption model and belonged to physical chemical mixed adsorption. The corrosion inhibition efficiency of HA was the highest at a concentration of 1500 ppm and enhanced with the extension of soaking time. After soaking for 72 h, the corrosion inhibition efficiency of HA reached its maximum (92.7%), indicating that HA had a good long-term corrosion inhibition effect. HA had a high adsorption energy on the surface of ADC12 aluminum alloy, and HA molecules adsorbed on its surface through the carboxyl groups linked to N atom to form a protective corrosion inhibitor film, effectively inhibiting its corrosion. [ABSTRACT FROM AUTHOR]

Chemical Enhanced Oil Recovery (CEOR) using polymers have recorded high sweep efficiency and favorable recovery. Polymers can be grouped into natural and synthetic polymers. The polyacrylamide (PAM) and xanthan gum (XG) are the most commonly utilized in polymer CEOR but XG is preferred for CEOR due to its tolerance to temperature, mechanical shear and salinity. XG have been utilized for field-scale CEOR studies but is very expensive to the economy of developing the countries. These exorbitant cost have driven to the search for suitable local alternatives which if successful, can improve CEOR and be exported to the global market. In this work, performance study was conducted to determine the potentials of polymer-low salinity flood to improve oil recovery. Terminalia mantaly exudate (TME) and Okra (OK) were utilized as local polymer while Xanthan gum (XG) was utilized as conventional polymers. FTIR characterization, aqueous stability, viscosity and core-flooding study were carried out in this study. From the FIIR study TME and OK recorded similar hydrophilic and hydrophobic functional group with XG, and can be categorized as polysaccharides. From Aqueous Stability study, TME, OK and XG all formed colloidal phase with water at higher temperature. From viscosity test, OK and XG recorded low viscosity tolerance in saline environment while TME recorded high viscosity tolerance in saline environment. From polymer flooding OK yielded additional 20% recovery while XG an TME recorded 17.33% and 16.89% additional recoveries respectively. In polymer-low salinity flooding, the CEOR additional crude oil recovery of OK, XG and TME increased by 11.1%, 7.7% and 7.9% respectively. The polymer-low salinity hybrid solution, recorded better recovery and this is due to synergy between the polymer an low salinity solution. [ABSTRACT FROM AUTHOR]

The characteristics and suitability of hydroxyapatite (HAP), tricalcium apatite phosphate (PTCa), and octocalcium apatite phosphate (OCPa), which possess similar attributes to those of an ideal adsorbent, were investigated to determine their efficacy in phenol removal. The aim of this paper is to assess the adsorption behavior of phenol on phosphates powders synthesized by the co-precipitation method at ambient temperature. Furthermore, the impact of initial phenol quantities and thermal conditions on the adsorption process was explored. X-ray diffraction analysis revealed the formation of HAP, PTCa, and OCPa structures under room temperature conditions. The sample morphologies were subjected to scrutiny utilizing MEB together with X-ray analysis. Additionally, chemical analysis revealed that Ca/P = 1.6, 1.5, and 1.33 for HAP, PTCa, and OCPa, respectively. The synthesized powders exhibited adsorption abilities of 2.86, 2.74, and 2.52 mg/g for HAP, PTCa, and OCPa, respectively, and reached equilibrium in approximately 80 minutes. The study revealed that the experimental data are appropriately represented by the Langmuir and Freundlich adsorption equations for HAP and PTCa, and Langmuir model in the case of OCPa, as well as by the pseudo-first-order and pseudo-second-order adsorption kinetics. Thermodynamic evaluations, including calculations of ΔG°, ΔH°, and ΔS°, were performed. The results indicated that the adsorption mechanisms exhibited physical characteristics, were thermally absorbing in the case of HAP and exothermic for the other two phosphates, PTCa and OCPa, and occurred spontaneously. [ABSTRACT FROM AUTHOR]

This work is a part of the project for investigations of hydrodynamics and mass transfer in an adsorption apparatus with ion-exchange resins during the extraction of stevioside from stevia extract. Nowadays the issues of improving the structural-sorption characteristics while increasing selectivity to certain substances, expanding the range, simplifying the manufacturing technology and reducing the cost of production of industrial adsorbents are extremely relevant. The submitted work is devoted to mathematical modeling and a theoretical description of adsorption in the layer of expanded ion-exchange resins. By this, the main aspects of adsorption in a layer of porous material have been considered, and a model of the geometric structure of the adsorption layer has been developed. The original contribution of the work and its scientific novelty lie in the fact that a mathematical model of the evolution of a two-component dispersed phase has been developed and qualitatively analyzed taking into account competitive adsorption and the non-equilibrium nature of mass transfer between the adsorption surface of the porous material and the dispersed phase. The results and conclusions of the work are recommended to be used in planning and conducting research work in the field of intensification of heat and mass transfer processes and engineering design of adsorption chemical apparatuses and adsorption columns. [ABSTRACT FROM AUTHOR]

The paper describes a simple analytical model that allows the calculation of hydrogen surface coverage under the influence of several processes that can co-occur during the ion-beam bombardment/sputter analysis of a sample surface, in particular during analysis by secondary ion mass spectrometry (SIMS). The model considers processes of dissociative adsorption, desorption, absorption from the surface into the sample volume, and removal by ion bombardment. After describing the model, we provide some examples of its practical applications for interpretation of the experimental results obtained during in situ SIMS studies of hydrogen interaction with the hydrogen-storage alloys TiFe, Zr2Fe, and with nickel. In the examples, some quantitative characteristics of surface-related processes involving hydrogen, such as hydrogen sputtering rate, activation energy of hydrogen desorption and absorption, have been successfully determined using various model approaches. [ABSTRACT FROM AUTHOR]

Combined heavy metal contamination in soil is a common phenomenon. Biochar amendment into the soil is considered to be an alternative for immobilization remediation of soil contaminated with heavy metals due to its adsorption and alkalization. However, much attention has been paid to the adsorption and immobilization of single heavy metals by biochar. In this paper, the competitive adsorption of Cd(II) and Zn(II) on biochar derived from cotton straw and pig manure at 500°C (BCS500 and BPM500), loess and biochar-loess mixtures were investigated using the batch equilibrium method. The results showed that the adsorption capacities of biochars, loess, and biochar-loess mixtures to Cd(II) and Zn(II) in the mixed Cd-Zn systems increased with the increase of initial metal concentrations of Cd(II) and Zn(II). The adsorptive capacities of BCS500 and BPM500 to Cd(II) in mixed Cd-Zn system were 33% and 35% less than those in the single Cd(II)systems, while the adsorptive capacities to Zn(II) were 62% and 56% less than those in the single Zn(II) systems. The adsorptive capacities of loess to Cd(II) and Zn(II) in mixed Cd-Zn systems were 29% and 55% less than those in the single metal systems. The adsorptive capacities of loess-BCS500 (LBCS) and loess-BPM500 (LBPM) to Cd(II) in mixed Cd-Zn system were 40% and 38% less than those in the single Cd(II) systems, while the adsorptive capacities to Zn(II) were 63% and 60% less than those in the single Zn(II)systems. Moreover, the competitive adsorptive capacity of Cd(II) is greater than that of Zn(II). It can be seen that when heavy metal pollution with similar nature of multiple elements exists in soil, the amount of adsorbent should be increased to resist the possible weakened adsorption caused by competitive adsorption in order to guarantee an effective absorption treatment. [ABSTRACT FROM AUTHOR]

Sodium adsorption on nanometer-thick-TiO2-channel thin-film transistors (TFTs) are examined for enhancing the drain current. In the TFTs, the channel thickness of TiO2 is set as thin as ∼16 nm. The TiO2 film is deposited by atomic layer deposition using plasma excited humified Ar, followed by crystallization into the anatase phase by thermal annealing at 500 °C in air. The gate oxide is a 300 nm thick SiO2 film, which is grown on a highly doped n+ Si substrate. The n+ Si substrate is used as the gate electrode. The drain and source electrodes of Ti are deposited by an electron beam evaporation at room temperature. The TiO2 channel is covered with multiple layers of aluminum silicate and SiO2 films to enhance the Na sorptivity. The multiple films consist of combinations of 1 nm thick SiO2 and 0.16 nm thick aluminum silicate. The channel length and width are 60 and 1000 μm, respectively. The TFT without the Na adsorption exhibits a field effect mobility of ∼0.5 cm2/V s, where the drain current is recorded around 30 μA with a gate voltage of 10 V. With immersion of the TFT in a 10 mM NaCl solution, the drain current is enhanced to the order of mA. The simulation with an equivalent circuit with source and drain resistances suggests that the field effect mobility is enhanced to ∼30 cm2/V s with the adsorption of Na. In this paper, we discuss the operation mechanism of the Na adsorbed TiO2 TFT and its applicability as TFT-based high current switch devices and sensors. [ABSTRACT FROM AUTHOR]

Context: To explore the impact of OGs (OGs) on formaldehyde (HCHO) adsorption by modified activated carbon, this paper studied the influence of OGs on HCHO adsorption characteristics, varying the groups including ester, carboxyl, and hydroxyl. Employing density functional theory (DFT), the effects of various OGs on the structure of N-doped activated carbon through GGA-PBE exchange-correlation functionals by Materials Studio combined with Gaussian software. The types of weak interactions during the adsorption process were calculated by RDG, elucidating the mechanism through which the three OGs affect HCHO adsorption on N-doped activated carbon. The dynamic adsorption process of HCHO was simulated by molecular dynamics (MD). The influence and proportion of OGs on HCHO adsorption were subsequently analyzed using van der Waals and electrostatic interactions, determining differences in formaldehyde adsorption effects across OG types. The carboxyl group exhibits the most robust synergistic adsorption effect on the modified activated carbon. There is a notable alteration in the position and distribution of electrostatic potential extremes observed following carboxyl modification. The calculation results show that the adsorption energy of hydroxyl groups on modified activated carbon is the highest, at −5.07 kcal/mol, with a transfer charge of 0.014 e. Following the introduction of carboxyl groups, the proportion of electrostatic interactions escalated from the initial 24% to 38%. This study will provide new ideas for guiding the design of activated carbon for efficient adsorption of formaldehyde. Methods: The modified activated carbon fragments of three OGs were constructed by Materials Studio and Gaussian software, and the surface electrostatic potential polarity and area distribution, charge change, adsorption energy, and transferred charge of each molecular fragment were calculated. Moreover, cell models of OGs with the same dimensions were constructed to simulate the adsorption amount, heat of adsorption, interaction energy, radial distribution function, and hydrogen-bonding interactions for methane at room temperature and pressure. The results were consistent with the DFT simulations. [ABSTRACT FROM AUTHOR]

Tetracycline hydrochloride (TCH) is widely used in medical, livestock breeding, and agricultural industries. However, because it is not fully absorbed by humans and animals while used, it enters environmental water bodies with feces and urine. TCH can damage the ecological environment, harm human health, and produce drug-resistant bacteria, posing threats to the environment and human health. Therefore, finding an economical and effective removal method is crucial for water quality safety. Currently, the removal methods for TCH in water mainly include chemical, biological, and physical methods. Compared with chemical and biological treatments, the adsorption method in physical treatments for removing TCH from polluted water bodies has the advantages of low cost, environmental friendliness, high efficiency, stability, and easy operation. In choosing adsorption materials, carbon-based and mineral materials often appear powdery, are not easily recoverable, and carry the risk of secondary pollution. In contrast, gel materials are suitable for removing organic pollutants. Thus, finding an inexpensive adsorbent with good adsorption performance is currently a hot subject. Montmorillonite (MMT) is a clay mineral with a stable crystal structure and high mechanical strength. It has a surface with many permanent negative charges. Due to its low cost, easy availability, and superior adsorption properties, it is commonly used in wastewater treatment to adsorb heavy metal ions, dyes, phenolic compounds, polycyclic aromatic hydrocarbons, etc., with good removal effects. However, there is currently no research specifically on using MMT for TCH adsorption. Against this background, this paper aims to study the adsorption performance and effects of MMT adsorbing TCH. Through research, it is found that the Freundlich isothermal adsorption model and the pseudo-second-order kinetic model fit well for MMT adsorbing TCH, indicating that its adsorption is multilayered and can reach 87% of the total adsorption amount within 60 minutes. The Langmuir saturation adsorption amount can reach 118.6mg/g. The Gibbs free energy ΔG0 is always negative, indicating that the adsorption of TCH by MMT is a spontaneous process. The calculated enthalpy and entropy changes are both positive, indicating that the adsorption process is endothermic and occurs randomly on the solid-liquid surface. Increasing the temperature promotes adsorption, which is consistent with the conclusions drawn from temperature effect experiments, further indicating that the adsorption process is an endothermic reaction and increasing the temperature is conducive to adsorption. The solution pH significantly affects adsorption performance. As the pH increases from 3 to 10, the adsorption amount first increases and then decreases, with the optimal pH range being 6-8. This is because, under strongly acidic conditions, H+ competes with TCH for adsorption, resulting in a lower adsorption amount of TCH by MMT. As the pH value increases and the H+ concentration decreases, the competitive adsorption with TCH is reduced, so the electrostatic adsorption of TCH by MMT increases. But as the pH continues to rise, TCH gradually transforms into H2TC- and HTC2- forms, creating electrostatic repulsion with negatively charged MMT and causing a decrease in adsorption. Based on the above experiment results and characterization analysis, the mechanism suggests that the adsorption process of MMT on TCH includes both physical adsorption and chemical actions, with the latter being dominant. The Al-O-H group in MMT can form hydrogen bonds with the tricarbamoyl amide and hydroxyl groups on the TCH molecule. At pH < 5, there is also a certain electrostatic attraction. In summary, due to the low cost of MMT, its fast adsorption rate, and high adsorption capacity, it has unique advantages in the adsorption performance of TCH, thus promising a bright application prospect in the actual TCH wastewater treatment. [ABSTRACT FROM AUTHOR]

[Display omitted] • By utilizing facile and low cost SILAR technique, a composite material comprising NiCo 2 S 4 and MnS was fabricated. • NiCo 2 S 4 is reported for the first time in the context of photodetector applications. • Extensive exploration of light wavelengths (300 nm to 700 nm) reveals the device's robust photo response, showcasing its versatility across the electromagnetic spectrum. • The device exhibits rising responsivities for UV (0.310 mA/W), visible (40.76 mA/W), and IR (0.07 mA/W) light, indicating its efficacy in diverse photodetection scenarios. • Demonstrating rapid response times (0.64 s UV, 1.16 s Visible, 0.58 s IR) further highlights the efficiency of the as-fabricated heterojunction device under varying light wavelengths. Photodetectors are pivotal components in modern electronics and energy harvesting systems, serving distinct yet essential roles. In the realm of next-generation electronics, traditional single-functional materials are no longer sufficient to meet evolving demands. In response to these challenges, we present a novel approach in which we develop a hetero-junction semiconductor composed of NiCo 2 S 4 /MnS. Through our research, we explore the effects of various light wavelengths on the photo response of the as-fabricated device. The heterojunction device was fabricated on a cellulose paper substrate using Successive Ionic Layer Adsorption and Reaction (SILAR) technique. X-ray diffraction (XRD) analysis confirmed the presence of the cubic phase of NiCo 2 S 4 and the hexagonal phase of γ MnS on the paper substrate, with Raman and FT-IR peaks validating the presence of both materials. Scanning electron microscopy (SEM) was employed to examine the thin film's morphology. Additionally, the UV–Vis absorption spectrum of the components was investigated, revealing bandgap values of 3.2 eV for MnS and 1.9 eV for NiCo 2 S 4 , justifying the device's response across a wide electromagnetic spectrum. The device exhibited rising responsivities of 0.310 mA/W for UV light, 40.76 mA/W for visible light, and 0.07 mA/W for IR light. Furthermore, the device demonstrated response times of 0.64 s (UV), 1.16 s (Visible), and 0.58 s (IR) when illuminated with light of varying wavelengths The as-fabricated heterojunction device holds the potential to serve as a promising candidate in photodetection. [ABSTRACT FROM AUTHOR]

[Display omitted] • Pore opening-induced pore blocking is the mechanism for the limit to LCP. • LCP is described for desorption of condensate from closed cavities with wedge-like opening. • Experimental LCP for carbons at P/P 0 ∼ 0.4 is reproduced in simulations at boiling points. • Experimental LCP for silica at P/P 0 ∼ 0.5 is described correctly in simulations. • LCP is relatively insensitive to the geometrical aspects of the cavity. The limit to the lower closure point (LCP) observed experimentally in the desorption isotherm of gases in porous solids has been commonly attributed to the homogeneous cavitation of the condensate in cavities. It was proposed recently that the experimental limit to LCP could be described in simulations with the ink-bottle pore, provided that the length of the uniformly sized conduit connecting the closed cavity to the surrounding is shorter than 2 nm, and the evaporation is by way of pore blocking mechanism, rather than homogeneous cavitation. To substantiate this assertion, that deviates from the commonly belief of homogeneous cavitation, we further investigated in this paper with cavities having wedge-like pore opening , that better mimics real solids, and offer further explanation on the limit of the LCP to the pore blocking as the mechanism of evaporation with simulations of argon and nitrogen adsorption over a range of temperatures that are commonly used experimentally. It was found that simulation results correctly captured the experimental observations for carbon-based materials and silica-based materials in that the limit of LCP shifts to higher reduced pressures for weaker adsorbing silica, compared to stronger adsorbing carbon and for a given adsorbent it also shifts to higher reduced pressure for higher temperatures. [ABSTRACT FROM AUTHOR]

Adsorption and advanced oxidation technology are important means to remove organic pollutants, and the combination of adsorption and catalytic degradation to construct a multi-field coupled system can realize valid adsorption and degradation of organic contaminants. In this paper, CuBi 2 O 4 supported by a nonmetallic element-modified graphene hydrogel composite structure CuBi 2 O 4 /X-rGH (X = N, P, S, B) was synthesized and applied to the efficient removal of organic pollutants. We found that the doping of nonmetallic elements enhances the graphene conjugated large π-bond system, which not only improves the adsorption performance of pollutants but also increases the graphene conductivity and builds more carrier transport channels, which is beneficial to the photocatalytic Fenton synergistic degradation activity. Among them, CuBi 2 O 4 /P-rGH could achieve 90 % degradation of phenol (50 ppm) after 20 min of turning on the light, which was nearly 2 times more than the degradation activity of CuBi 2 O 4 /rGH. Electron paramagnetic resonance (EPR) and quenching experiments proved that ·OH was the main active species in the synergistic degradation process, and the mechanism of adsorption of nonmetallic modified graphene hydrogel hybrid catalysts and in situ photocatalytic Fenton degradation of pollutants was proposed. [ABSTRACT FROM AUTHOR]

Tight gas reservoirs with mobile water exhibit multi-phase flow and high stress sensitivity. Accurately analyzing the reservoir and well parameters using conventional single-phase rate transient analysis methods proves challenging. This study introduces novel rate transient analysis methods incorporating evaluation processes based on the conventional flowing material balance method and the Blasingame type-curve method to examine fractured gas wells producing water. By positing a gas-water two-phase equivalent homogenous phase that considers characteristics of mobile water, gas, and high stress sensitivity, the conventional single-phase rate transient analysis methods can be applied by integrating the phase's characteristics and defining the phase's normalized parameters and material balance pseudotime. The rate transient analysis methods based on the equivalent homogenous phase can be used to quantitatively assess the parameters of wells and gas reservoirs, such as original gas-in-place, fracture half-length, reservoir permeability, and well drainage radius. This facilitates the analysis of production dynamics of fractured wells and well-controlled areas, subsequently aiding in locating residual gas and guiding the configuration of well patterns. The specific evaluation processes are detailed. Additionally, a numerical simulation mechanism model was constructed to verify the reliability of the developed methods. The methods introduced have been successfully implemented in field water-producing gas wells within tight gas reservoirs containing mobile water. [ABSTRACT FROM AUTHOR]