Since the discovery of carbon dots(CDs)in 2004,the unique photoluminescence phenomenon of CDs has attracted widespread attention.However,the molecular weight of CDs has not been adequately quantified at present,due to...Since the discovery of carbon dots(CDs)in 2004,the unique photoluminescence phenomenon of CDs has attracted widespread attention.However,the molecular weight of CDs has not been adequately quantified at present,due to CDs are atomically imprecise and their molecular weight distribution is broad.In this paper,a series of Pluronic-modified CDs were prepared and the structure of the CDs was briefly analyzed.Subsequently,a molecular weight measurement method based on colligative properties was developed,and the correction coefficient in the algorithm was briefly analyzed.The calculated molecular weight was applied to the determination of surface adsorption capacity.This work provided a method for averaging the molecular weight of atomically imprecise particulate materials,which is expected to provide new opportunities in related fields.展开更多
Due to the existence of water content in shale reservoir,it is quite meaningful to clarify the effect of water content on the methane adsorption capacity(MAC)of shale.However,the role of spatial configuration relation...Due to the existence of water content in shale reservoir,it is quite meaningful to clarify the effect of water content on the methane adsorption capacity(MAC)of shale.However,the role of spatial configuration relationship between organic matter(OM)and clay minerals in the MAC reduction process is still unclear.The Silurian Longmaxi Formation shale samples from the Southern Sichuan Basin in China were prepared at five relative humidity(RH)conditions(0%,16%,41%,76%,99%)and the methane adsorption experiments were conducted on these water-bearing shale samples to clarify the MAC reduction process considering the spatial configuration relationship between clay minerals and OM and establish the empirical model to fit the stages.Total organic carbon(TOC)content and mineral compositions were analyzed and the pore structures of these shale samples were characterized by field-emission scanning electron microscopy(FE-SEM),N2 adsorption and high-pressure mercury intrusion porosimetry(HPMIP).The results showed that the MAC reduction of clay minerals in OM occurred at different RH conditions from that of clay minerals outside OM.Furthermore,the amount of MAC reduction of shale samples prepared at the same RH condition was negatively related with clay content,which indicated the protection role of clay minerals for the MAC of water-bearing shale samples.The MAC reduction process was generally divided into three stages for siliceous and clayey shale samples.And the MAC of OM started to decline during stage(1)for calcareous shale sample mainly because water could enter OM pores more smoothly through hydrophobic pathway provided by carbonate minerals than through hydrophilic clay mineral pores.Overall,this study will contribute to improving the evaluation method of shale gas reserve.展开更多
The variations of strain and permeability of coal were systematically studied through the physical simulation of N2 and water injection.The effects of fluid adsorption capacity and initial permeability on strain,perme...The variations of strain and permeability of coal were systematically studied through the physical simulation of N2 and water injection.The effects of fluid adsorption capacity and initial permeability on strain,permeability and the dominant effect of pore pressure were discussed.The adsorption strain and strain rate of coal during water injection are significantly higher than those during N2 injection.An edge of free adsorption exists in the early phase of N2 and water injection,which is related to fluid saturation.Within this boundary,the strain rate and pore pressure are independent.Moreover,the injec-tion time of initial stage accounts for about 20%of the total injection time,but the strain accounts for 70%of the total strain.For water injection,this boundary is about half of water saturation of coal.Besides,the influence of pore pressure on permeability is complex,which is controlled by adsorption capacity and initial permeability of coal.When the initial permeability is large enough,the effect of adsorption strain on permeability is relatively weak,and the promoting effect of pore pressure on fluid migration is dominant.Therefore,the permeability increases with increasing pore pressure.When the initial permeability is relatively low,the pore pressure may have a dominant role in promoting fluid migration for the fluid with weak adsorption capacity.However,for the fluid with strong adsorption capacity,the adsorption strain caused by pore pressure may play a leading role,and the permeability reduces first and then ascends with increasing pore pressure.展开更多
Coal fly ash （CFA） generated by coal-based thermal power plants is mainly composed of some oxides having high crystallinity, including quartz and mullite. In this study, the effect of CFA crystallinity toward its ca...Coal fly ash （CFA） generated by coal-based thermal power plants is mainly composed of some oxides having high crystallinity, including quartz and mullite. In this study, the effect of CFA crystallinity toward its capacity on Pb（Ⅱ） adsorption was investigated. CFA with various crystaUinity was obtanied by refluxing it with sodium hydroxide （NaOH） solution having various concentrations （1-7 M） at various temperature and reflux time. To evaluate the effect of crystallinity of treated CFA on the adsorption capacity, adsorption of Pb（Ⅱ） solution with treated CFA was carried out. The research shows that the reflux of CFA with NaOH solution leads to the crystallinity of quartz and mullite in CFA decreased. The decrease is proportional with the concentration increasing, the temperature elevation, and the longer time. The reflux using NaOH solution with high concentration （〉 3 M） in addition causes a decrease in the crystallinity of quartz and mullite, also results in the formation of hydroxysodalite. The decrease of the CFA crystalllinity gives an increase in CFA adsorption capacity toward Pb（Ⅱ） solution.展开更多
The static adsorption performances of a series of active carbon fiber(ACF)for xenon at 201 K were measured with a model ASAP2010M specific surface area and aperture distribution instrument by changing the working gas ...The static adsorption performances of a series of active carbon fiber(ACF)for xenon at 201 K were measured with a model ASAP2010M specific surface area and aperture distribution instrument by changing the working gas of instrument from N 2 to Xenon. Compared with grain active carbon(GAC): (1) the adsorption performance of Viscose based ACF(VACF) adsorbents is better than that of GAC; (2) owing to the difference of aperture distribution, the adsorption performance of ACF with different radicales is different under the same experiment conditions though the specific surface area is similar; (3) there is no definite relationship between adsorption performance and specific surface area; (4) the VACF A2 is the superior xenon adsorbent at the experimental temperature.展开更多
Organic matter(OM)is the primary gas occurrence carrier in shale reservoirs due to their abundant nanopores.To reveal the OM pore structure,adsorption capacity and evolution during thermal maturation,this study collec...Organic matter(OM)is the primary gas occurrence carrier in shale reservoirs due to their abundant nanopores.To reveal the OM pore structure,adsorption capacity and evolution during thermal maturation,this study collected data from samples spanning the entire evolution stage,from immature to over-mature.Scanning Electron Microscope(SEM)observation and low temperature gases adsorption experiments were used to qualitatively-semi-quantitatively and quantitatively analyze OM pore structure evolution,and CH_(4) isothermal adsorption experiments were used to reveal the adsorption capacity evolution.Then,the influence and mechanism of matu rity and hydrocarbon generation on pore development and adsorption capacity were quantitatively reviewed based on the experimental data.The results show that OM pores are poorly developed in the immature stage due to weak hydrocarbon generation,although micro-fractures are occasionally found at the edges of OM particles.In the low maturity stage,OM pores are partially developed due to liquid hydrocarbon generation,with liquid hydrocarbons also filling some OM pores.The contribution of total organic carbon content(TOC)to adsorption extent is not significant in these two stages.From high to high-over maturity stages,massive gaseous hydrocarbons are generated,significantly improving the surface porosity of OM.Clear positive linear correlations are observed between TOC and adsorption amount.However,the development of OM pores significantly declines when thermal maturity(R_(o))exceeds 3.5%due to excessive aromatization.The accuracy of research on the evolution of pore structure and adsorption capacity is limited by several factors:(ⅰ)errors caused by sample specification,calculation processes,parameter settings,and kerogen models in isothermal adsorption experiments and molecular simulations;(ⅱ)difficulty in achieving control variables due to the strong heterogeneity of natural maturation shale samples;and(ⅲ)the need to enhance compatibility between thermal simulation experiments and natural thermal evolution.Therefore,isothermal adsorption experiments on bulk shale and molecular simulations of intact shale model are necessary,taking into account the dynamic temperature and pressure of in-situ reservoirs.Moreover,shale samples with varying maturity,influenced by their distance from the paleo-thermal source,may provide significant verification for thermal simulation experiments.展开更多
The purpose of this research work is to determine the removal efficiency of Cu^(2+)and Pb^(2+)ions using polyvinyl alcohol/neem leaf extract/chitosan(PVA/NLE/CS)composite films as adsorbent materials from an aqueous m...The purpose of this research work is to determine the removal efficiency of Cu^(2+)and Pb^(2+)ions using polyvinyl alcohol/neem leaf extract/chitosan(PVA/NLE/CS)composite films as adsorbent materials from an aqueous medium,with respect to pH,contact time,and adsorbent dosage.The synthesized composite material was characterized using Fourier Transform Infrared(FTIR)spectroscopy,thermogravimetric analysis-Derivative Thermogravimetry(TGA-DTG),X-ray diffraction(XRD),X-ray photoelectron spectroscopy(XPS),and scanning electron microscopy-Energy Dispersive X-ray Spectroscopy(SEM-EDX).The antibacterial activity and swelling response of the material were studied using suitable methodologies.The FTIR study confirmed the interactions among PVA,chitosan,and neem leaf extract.The TGA data reveal the excellent thermal stability of the developed composite films.The SEM micrograph indicates a homogeneous phase morphology with good compatibility among chitosan,the monomer,and the leaf extract.The antibacterial study revealed that the prepared PVA/NLE/CS films exhibit improved antibacterial activity against bacterial growth.It was found that at pH 6.0,the adsorption capacity for both toxic metal ions is maximum,and decreases with a further rise in pH.At this pH,the adsorption capacity of PVA/NLE/CS films increases with a gradual increase in adsorbent dosage,and at a specific pH,the adsorption capacity for Cu^(2+)is greater than that for Pb^(2+).The adsorption efficiency is a function of contact time and was found to be maximal at 180 min.Hence,the developed composite material is effective for the removal of metal ions from wastewater.展开更多
A novel adsorbent was prepared by modifying orange peel with sodium hydroxide and calcium chloride. The morphological and characteristics of the adsorbent were evaluated by infrared spectroscopy （IR）, scanning elect...A novel adsorbent was prepared by modifying orange peel with sodium hydroxide and calcium chloride. The morphological and characteristics of the adsorbent were evaluated by infrared spectroscopy （IR）, scanning electron microscopy （SEM） and N2-adsorption techniques. The adsorption behavior of Cu^2＋, Pb^2＋ and Zn^2＋ on modified orange peel （SCOP） was studied by varying parameters like pH, initial concentration of metal ions. Equilibrium was well described by Langmuir equation with the maximum adsorption capacities for Cu^2＋, Pb^2＋ and Zn^2＋ of 70.73, 209.8 and 56.18 mg/g, respectively. Based on the results obtained in batch experiments, breakthrough profiles were examined using a column packed with SCOP for the separation of small concentration of Pb^2＋ from an excess of Zn^2＋ followed by elution tests. Ion exchange with Ca^2＋ neutralizing the carboxyl groups of the pectin was found to be the predominant mechanism.展开更多
CCUS (carbon capture, utilization, and storage) technology is regarded as a bottom method to achieve carbon neutrality globally. CO_(2) storage in deep coal reservoirs serves as a feasible selection for CCUS, and its ...CCUS (carbon capture, utilization, and storage) technology is regarded as a bottom method to achieve carbon neutrality globally. CO_(2) storage in deep coal reservoirs serves as a feasible selection for CCUS, and its storage potential can be attributed to the CO_(2) adsorption capacity of the coal. In this paper, a series of CO_(2) adsorption isotherm experiments were performed at different pressures and temperatures in sub-bituminous coal from the southern Junggar Basin (reservoir temperature ∼25.9°C and pressure ∼3.91 MPa). In addition, the high-pressure CO_(2) adsorption characteristics of the southern Junggar Basin coal were characterized using a supercritical D-R adsorption model. Finally, the CO_(2) storage capacities in sub-bituminous coal under the in situ reservoir temperature and pressure were analyzed. Results indicated that the excess adsorption capacities increase gradually with increasing injection pressure before reaching an asymptotic maximum magnitude of ∼34.55 cm3/g. The supercritical D-R adsorption model is suitable for characterizing the excess/absolute CO_(2) adsorption capacity, as shown by the high correlation coefficients > 0.99. The CO_(2) adsorption capacity increases with declining temperature, indicating a negative effect of temperature on CO_(2) geological sequestration. By analyzing the statistical relationships of the D-R adsorption fitting parameters with the reservoir temperature, a CO_(2) adsorption capacity evolution model was established, which can be further used for predicting CO_(2) sequestration potential at in situ reservoir conditions. CO_(2) adsorption capacity slowly increases before reaching the critical CO_(2) density, following a rapid decrease at depths greater than ∼800 m in the southern Junngar Basin. The research results presented in this paper can provide guidance for evaluating CO_(2) storage potential in deep coal seams.展开更多
Determination of gas adsorption capacity under geological conditions is essential in evaluating shale gas resource potential.A quantitative determination of gas adsorption capacity was proposed through 1)investigating...Determination of gas adsorption capacity under geological conditions is essential in evaluating shale gas resource potential.A quantitative determination of gas adsorption capacity was proposed through 1)investigating controlling geological factors(including both internal ones and external ones)of gas adsorption capacity in organic-rich marine shale with geochemical analysis,XRD diffraction,field-emission scanning electron microscopy,and methane sorption isotherms;2)defining the relationship between gas adsorption capacity and single controlling factor;3)establishing a comprehensive determination model with the consideration of all these controlling factors.The primary controlling factors of the sorption capacity for the studied O3wLower S1l shale are TOC,illite and quartz,temperature,pressure,Ro,and moisture(water saturation).Specifically,TOC,thermal maturity,illite,and pressure are positively correlated with sorption capacity,whereas,quartz and temperature contribute negatively to the sorption capacity.We present the quantitative model along with application examples from the Wufeng-Lower Longmaxi Shale in the southeast Sichuan Basin,west China,to demonstrate the approach in shale gas evaluation.The result shows that the comprehensive determination model provides a good and unbiased estimate of gas adsorption capacities with a high correlation coefficient(0.96)and bell-shaped residues centered at zero.展开更多
The goal of this work is to improve the simultaneous removal of Pb2+, Cu2+, Zn2+, and Cd2+ ions from synthetic wastewater in a fixed bed column by incorporating sodium dodecyl sulfate (SDS) onto the surface of activat...The goal of this work is to improve the simultaneous removal of Pb2+, Cu2+, Zn2+, and Cd2+ ions from synthetic wastewater in a fixed bed column by incorporating sodium dodecyl sulfate (SDS) onto the surface of activated carbon made from coconut shells. The activated carbons were characterized using Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy-energy dispersive x-ray (SEM-EDX). The adsorption column dynamics were studied by varying the flow rates (5, 10 and 15 mL/min), bed heights (10, 15 and 20 cm), and initial concentrations (50, 150, and 250 mg/L). The activated carbon has a pore volume of 0.715 cm3/g and a BET-specific surface area of 1410 m2/g. Sodium dodecyl sulfate (SDS) surfactant incorporation onto the surface of the activated carbon enhances its capacity for simultaneous adsorption of Pb2+, Cu2+, Zn2+, and Cd2+ from the aqueous medium. The affinity of the heavy metals to both unmodified (AC) and modified (AC-SDS) activated carbons followed the order of Pb2+ > Cu2+ > Zn2+ > Cd2+. The dynamic adsorption of the column depends on the flow rate, bed height, initial metal concentration, and SDS surface modification. With a 5 mL/min flow rate, a 20 cm bed height, and a 50 mg/L initial metal concentration, a maximum break-through time of 150 minutes for the unmodified activated carbon (AC) and 180 minutes for the SDS-modified activated carbon (AC-SDS) was reached.展开更多
Increased human and industrial activities have exacerbated the release of toxic materials and acute envi-ronmental pollution in recent times.Biochar,a carbon-rich material produced from biomass,is gaining momentum as ...Increased human and industrial activities have exacerbated the release of toxic materials and acute envi-ronmental pollution in recent times.Biochar,a carbon-rich material produced from biomass,is gaining momentum as a versatile material for attaining a sustainable environment.The study reviews the application of functionalized biochar for energy storage,environmental remediation,catalysis,and sustainable agriculture,aiming to achieve a greener future.Thedeployment of crop residues as a renewable feedstock for biochar,and their properties,compositions,modification,and functionalization techniques are also discussed.Additionally,the avenues for applying functionalized biochar to achieve a greener future,future trends and innovations,challenges,and future research directions are highlighted.Despite the limitations of scalability,ecotoxicological risks,logistical issues,lack of characterization protocols,high production costs,poor social acceptance,and inadequate policy and regulatory frameworks,functionalized biochar offers a better surface area,improved porosity,enhanced functional groups,and higher recoverability,leading to improved performance,adsorption capacity,biodegradability,and applications in specialized fields.Future research should prioritize standardization,scalability,cost reduction strategies,expansion of application areas,integration of emerging tools such as artificial intelligence and predictive modeling,and the development of policy and regulatory frameworks,ensuring that biochar’s full potential is harnessed effectively to support a low-carbon,resource-efficient future and global sustainability goals.展开更多
Aluminum hydroxide adjuvant exhibits a poorly crystalline boehmite(PCB)structure,which demonstrates instability during prolonged storage.In the present study,we systematically investigated the quality alterations of t...Aluminum hydroxide adjuvant exhibits a poorly crystalline boehmite(PCB)structure,which demonstrates instability during prolonged storage.In the present study,we systematically investigated the quality alterations of the adjuvant stored at roo m temperature by analyzing its crystal structure,particle size distribution,electron microscopic characteristics,pH,isoelectric point(pI),and adsorption capacity.These assessments aimed to ensure the effectiveness and safety of vaccine production.Three batches of adjuvants were stored at room temperature for 15 months,and their changes were monitored using X-ray diffraction patterns,transmission electron microscopy(TEM),pH measurements,pI determination,and adsorption capacity analysis.X-ray diffraction revealed that the crystalline phases of aluminum hydroxide initially exhibited a PCB structure,which became progressively more ordered during storage.Notably,after 12 months,a new diffraction peak emerged at 18.2°2θ,with its intensity increasing over time.This corresponded to the formation of highly crystalline gibbsite and bayerite,which compromised the stability of the adjuvant.Furthermore,the pH and pI values decreased during storage,reflecting a decline in the chemical stability of the adjuvant.Comprising nanoparticles with a mean diameter of 130 nm,the adjuvant maintained a high surface area and excellent adsorption capacity.The adsorption rate at 8 mg BSA/mg Al3+consistently exceeded 97%,with no statistically significant differences observed between the adsorption capacities at 1 and 15 months(P>0.05).This indicated that the nanoparticle aluminum hydroxide adjuvant sustained high adsorption efficiency throughout the storage period,underscoring its reliability as a vaccine adsorbent.However,in the later stages of storage,the emergence of highly crystalline gibbsite and bayerite,coupled with declines in pH and pI,negatively impacted the adjuvant’s stability.Based on these findings,we recommended that aluminum hydroxide adjuvants should not be stored at room temperature for longer than 12 months to preserve their quality and efficacy.展开更多
The aluminum hydroxide adjuvant possesses a poorly crystalline boehmite (PCB) structure, the stability of which is significantly affected by storage conditions. In the present study, we conducted a comprehensive inves...The aluminum hydroxide adjuvant possesses a poorly crystalline boehmite (PCB) structure, the stability of which is significantly affected by storage conditions. In the present study, we conducted a comprehensive investigation into the structural and quality alterations of aluminum hydroxide adjuvants under varying temperature conditions over time. Three batches of the adjuvant were stored at 2–8℃, 18–25℃, and 37℃, respectively, for 6 months. Key parameters, including X-ray diffraction patterns, pH, isoelectric point (pI), adsorption capacity, and average particle size, were analyzed to assess the impact of storage temperatures. X-ray diffraction analysis confirmed the PCB structure of the aluminum hydroxide adjuvant. Notably, after 1 month of storage at 37℃, new diffraction peaks emerged at 18.2 °2θ, with their intensity increasing progressively over time. Concurrently, the largest decreases in pI and pH were observed, measuring 0.78 and 1.33, respectively. In contrast, adjuvants stored at 2–8℃ for 6 months exhibited only faint diffraction peaks at 18.2 °2θ, indicating minor structural changes. Under these conditions, the reductions in pI and pH were comparatively smaller, at 0.43 and 0.80, respectively. The average particle size of the adjuvants remained within 110–140 nm across all storage conditions. Additionally, the aluminum hydroxide adjuvant consistently demonstrated a high protein adsorption capacity, approximately 8 mg BSA/mg Al^(3+), with no statistically significant differences in adsorption rates observed among the different temperature conditions (P > 0.05). These findings highlighted the remarkable adsorption efficiency of nanoparticle aluminum hydroxide adjuvants throughout storage, reinforcing their potential as superior vaccine adsorbents. However, elevated storage temperatures were shown to accelerate structural aging, promoting the formation of highly crystalline phases such as gibbsite or bayerite, which could compromise the stability and quality of the adjuvant.展开更多
Controlling surface chemistry is critically important for improving the initial Coulombic efficiency(ICE)and adsorption capacity of hard carbon anode used in Li/Na/K-ion batteries.However,accurately identifying the ty...Controlling surface chemistry is critically important for improving the initial Coulombic efficiency(ICE)and adsorption capacity of hard carbon anode used in Li/Na/K-ion batteries.However,accurately identifying the types and concentrations of hydrogen/oxygen terminated functional groups(HTFG/OTFGs)and distinguishing their functionalities remain challenge.Herein,we quantitatively investigated the surface chemistry on hard carbon via ultra-high temperature programed desorption measurements,and uncovered the role of HTFG/OTFGs in influencing ICE and adsorption capacity in Li/Na/K-ions cells.The C-H group is found to be dominant species on the surface of hard carbon,and presents a positive correlation with ICE values and adsorption capacity.The low reactivity of C-H group with both electrolyte salt and solvent results in the formation of thinner and highly conducive solid electrolyte interphase(SEI)layer,which benefit for the enhanced ICE and improved Li/Na/K-ions diffusion across SEI layer.Additionally,the pimping trapping effect of C-H groups allows the adsorbed Li/Na/K-ions to migrate into graphitic interlayer quickly,enhancing the slope capacity.By fabricating a C-H group-rich surface chemistry on hard carbon,a high ICE value and satisfactory specific capacity have been realized.These findings enrich our understanding of the surface chemistry-induced interfacial reaction,which effectively guides the rational design of high-performance hard carbon.展开更多
Wastewater plays a crucial role in deteriorating water quality and can significantly affect human health and ecosystems if discharged without proper treatment.Among available treatment methods,adsorption is often cons...Wastewater plays a crucial role in deteriorating water quality and can significantly affect human health and ecosystems if discharged without proper treatment.Among available treatment methods,adsorption is often considered an effective,relatively inexpensive,and environmentally friendly purification technique,but its efficiency depends on the sorbents used.The use of low-cost biosorbents with high adsorption capacity is widely studied.These include various biomaterials such as microalgae,cyanobacteria,fungi,and plant materials.The utilization of different biosorbents derived from plant waste,such as Paulownia wood,aspen,hickory,Ziziphus bark,peach tree shavings,as well as grasses such as red fescue and reed,and Sargassum algae in natural and modified forms,is a crucial research direction.Such studies highlight the potential to address waste issues by repurposing it as biosorbents.Several studies have examined the ability of different biosorbents to treat wastewater and suggested that the physicochemical properties of the material's surface,such as specific surface area,pore size,and pore volume,play a decisive role in adsorption capacity.A quantitative analysis of plant-based biosorbents will significantly aid in developing water treatment systems and achieving optimal adsorption through modifications of their physicochemical properties.Furthermore,the analysis will help understand the relative importance of each physicochemical property in determining adsorption capacity,thereby contributing to the implementation of treatment methods targeting specific pollutants.展开更多
In order to improve the calculation method of the isosteric adsorption heat,clarify thermodynamic characteristics of CH4 adsorption by continental shale and reveal the adsorption mechanism,this paper selected shale sa...In order to improve the calculation method of the isosteric adsorption heat,clarify thermodynamic characteristics of CH4 adsorption by continental shale and reveal the adsorption mechanism,this paper selected shale samples from the seventh Member of Yanchang Formation of Upper Triassic in the Yanchang Gasfield of the Ordos Basin as the research object.The isothermal adsorption experiment was carried out on the CH4 adsorption by continental shale and the excess adsorption curves were plotted.Then,the characteristics of the isosteric adsorption heat of the shale with different types of adsorption capacity were illustrated by analyzing and comparing the difference between excess and absolute adsorption capacity.And the following research results were obtained.First,under the same temperature and pressure,absolute adsorption capacity is higher than the excess values.The difference between them is higher under low temperature and high pressure and it is in the relationship of exponential function with the equilibrium pressure.If excess adsorption capacity is used to evaluate the adsorptive property of shale reservoirs,the evaluation result will be underestimated.Second,for CH4 adsorption by Yanchang Formation shale,the absolute and excess isosteric adsorption heat values have a linear positive correlation with absolute and excess adsorption capacity respectively,and the intermo-lecular force of adsorbate has a dominant effect on isosteric adsorption heat values.Third,absolute isosteric adsorption heat value is less than the excess heat.The relative error is in the range of 18.18e49.79%,and it is higher in the stage with low adsorption capacity.If excess adsorption capacity is taken as the basic data to calculate initial isosteric adsorption heat values,the calculation result will be overvalued,and consequently,the evaluation of the intermolecular force of adsorbent and adsorbate is overestimated.展开更多
Constructed wetlands （CWs） are engineered systems that utilize natural systems including wetland vegetations, soils, and their associated microbial assemblages to assist in treating wastewater. The kinetic adsorptio...Constructed wetlands （CWs） are engineered systems that utilize natural systems including wetland vegetations, soils, and their associated microbial assemblages to assist in treating wastewater. The kinetic adsorption of ammonium nitrogen （NH＋-N） by CW substrate materials such as blast furnace slag （BFS）, zeolite, ceramsite, vermiculite, gravel, paddy soil, red soil, and turf, was investigated using batch experiments and kinetic adsorption isotherms. Both Freundlich and Lang- muir isotherms could adequately predict the NH＋-N adsorption process. The maximum adsorption capacities of NH＋-N, estimated from the Langmuir isotherm, ranked as： zeolite （33 333.33 mg kg^-1） 〉 turf （29274.01 mg kg^-1） 〉 BFS （5000 mg kg^-1） 〉 vermiculite （3333.33 mg kg^-1） 〉 gravel （769.23 mg kg^-1） 〉 paddy soil （588.24 mg kg^-1） 〉 red soil （555.56 mg kg^-1） 〉 ceramsite （107.53 mg kg^-1）. Some properties of the substrate materials, including bulk density, specific gravity, hydraulic conductivity, uniformity coefficient （K60）, curvature coefficient （Co）, organic matter, pH, exchangeable （or active） Cu, Fe, Zn and Mn, total Cu, and Fe, Mn, Zn, Cd, Pb and Ca, had negative correlations with NH＋-N adsorption. Other properties of the substrate materials like particle diameter values of D10, 030 and 060 （the diameters of particle sizes of a substrate material at which 10%, 30% and 60%, respectively, of the particles pass through the sieve based on the accumulative frequency）, cation exchange capacity （CEC）, exchangeable （or active） Ca and Mg, and total K and Mg had positive correlations with NH＋-N adsorption. In addition, active K and Na as well as the total Na had significant positive correlations with NH＋-N adsorption. This information would be useful for selection of suitable substrate materials for CWs.展开更多
In this paper, the methane adsorption behaviours in slit-like chlorite nanopores were investigated using the grand canonical Monte Carlo simulation method, and the influences of the pore sizes, temperatures, water, an...In this paper, the methane adsorption behaviours in slit-like chlorite nanopores were investigated using the grand canonical Monte Carlo simulation method, and the influences of the pore sizes, temperatures, water, and compositions on methane adsorption on chlorite were discussed. Our investigation revealed that the isosteric heat of adsorption of methane in slit-like chlorite nanopores decreased with an increase in pore size and was less than 42 kJ/mol, suggesting that methane adsorbed on chlorite through physical adsorption. The methane excess adsorp- tion capacity increased with the increase in the pore size in micropores and decreased with the increase in the pore size in mesopores. The methane excess adsorption capacity in chlorite pores increased with an increase in pressure or decrease in pore size. With an increase in temperature, the isosteric heats of adsorption of methane decreased and the methane adsorption sites on chlorite changed from lower- energy adsorption sites to higher-energy sites, leading to the reduction in the methane excess adsorption capacity. Water molecules in chlorite pores occupied the pore wall in a directional manner, which may be related to the van der Waals and Coulomb force interactions and the hydrogen bonding interaction. It was also found that water molecules existed as aggregates. With increasing water content, the water molecules occupied the adsorption sites and adsorption space of the methane, leading to a reduction in the methane excess adsorption capacity. The excess adsorption capacity of gas on chlorite decreased in the following order： carbon dioxide 〉 methane 〉 nitrogen. If the mole fraction of nitrogen or carbon dioxide in the binary gas mixture increased, the mole fraction of methane decreased, methane adsorption sites changed, and methane adsorption space was reduced, resulting in the decrease in the methane excess adsorption capacity.展开更多
A semi-empirical adsorption kinetic model was proposed with the time compensation method to describe the chemisorption of SO2 in flue gas by carbon adsorbents for flue gas purification.The change in adsorption capacit...A semi-empirical adsorption kinetic model was proposed with the time compensation method to describe the chemisorption of SO2 in flue gas by carbon adsorbents for flue gas purification.The change in adsorption capacity and adsorption rate with time at different water vapor concentrations and different SO2 concentrations was studied.The model was in good agreement with experimental data.The surface reaction was probably the rate controlling step in the early stage for SO2 adsorption by ZL50 activated carbon.The parameters m and n in the nth order adsorption kinetic model were related to the magnitude of the time compensation and adsorption driving force,respectively.The change of parameter n with water vapor concentrations and sulfur dioxide concentrations was studied and some physical implications were given.The sum of square errors was less than 1.0 and the average absolute percentage deviations ranged from 0.5 to 3.2.The kinetic model was compared with other models in the literature.展开更多
文摘Since the discovery of carbon dots(CDs)in 2004,the unique photoluminescence phenomenon of CDs has attracted widespread attention.However,the molecular weight of CDs has not been adequately quantified at present,due to CDs are atomically imprecise and their molecular weight distribution is broad.In this paper,a series of Pluronic-modified CDs were prepared and the structure of the CDs was briefly analyzed.Subsequently,a molecular weight measurement method based on colligative properties was developed,and the correction coefficient in the algorithm was briefly analyzed.The calculated molecular weight was applied to the determination of surface adsorption capacity.This work provided a method for averaging the molecular weight of atomically imprecise particulate materials,which is expected to provide new opportunities in related fields.
基金supported by the National Science and Technology Major Project of China(No.2017ZX05035-002)the National Natural Science Foundation of China(No.41972145)the Foundation of State Key Laboratory of Petroleum Resources and Prospecting from China University of Petroleum in Beijing(Nos.PRP/indep-3-1707,PRP/indep-3-1615)。
文摘Due to the existence of water content in shale reservoir,it is quite meaningful to clarify the effect of water content on the methane adsorption capacity(MAC)of shale.However,the role of spatial configuration relationship between organic matter(OM)and clay minerals in the MAC reduction process is still unclear.The Silurian Longmaxi Formation shale samples from the Southern Sichuan Basin in China were prepared at five relative humidity(RH)conditions(0%,16%,41%,76%,99%)and the methane adsorption experiments were conducted on these water-bearing shale samples to clarify the MAC reduction process considering the spatial configuration relationship between clay minerals and OM and establish the empirical model to fit the stages.Total organic carbon(TOC)content and mineral compositions were analyzed and the pore structures of these shale samples were characterized by field-emission scanning electron microscopy(FE-SEM),N2 adsorption and high-pressure mercury intrusion porosimetry(HPMIP).The results showed that the MAC reduction of clay minerals in OM occurred at different RH conditions from that of clay minerals outside OM.Furthermore,the amount of MAC reduction of shale samples prepared at the same RH condition was negatively related with clay content,which indicated the protection role of clay minerals for the MAC of water-bearing shale samples.The MAC reduction process was generally divided into three stages for siliceous and clayey shale samples.And the MAC of OM started to decline during stage(1)for calcareous shale sample mainly because water could enter OM pores more smoothly through hydrophobic pathway provided by carbonate minerals than through hydrophilic clay mineral pores.Overall,this study will contribute to improving the evaluation method of shale gas reserve.
基金supported by the National Natural Science Foundation of China(41872170,42072189)China Postdoctoral Science Foundation(2021M690916)+3 种基金Key Science and Technology Program of Henan Province(222102320154)State Key Laboratory Cultivation Base for Gas Geology and Gas Control(Henan Polytechnic University)(WS2020B10)Key Scientific Research Projects of Colleges and Universities in Henan Province(21A440006)Doctor foundation of Henan Polytechnic University(B2020-6,B2021-5).
文摘The variations of strain and permeability of coal were systematically studied through the physical simulation of N2 and water injection.The effects of fluid adsorption capacity and initial permeability on strain,permeability and the dominant effect of pore pressure were discussed.The adsorption strain and strain rate of coal during water injection are significantly higher than those during N2 injection.An edge of free adsorption exists in the early phase of N2 and water injection,which is related to fluid saturation.Within this boundary,the strain rate and pore pressure are independent.Moreover,the injec-tion time of initial stage accounts for about 20%of the total injection time,but the strain accounts for 70%of the total strain.For water injection,this boundary is about half of water saturation of coal.Besides,the influence of pore pressure on permeability is complex,which is controlled by adsorption capacity and initial permeability of coal.When the initial permeability is large enough,the effect of adsorption strain on permeability is relatively weak,and the promoting effect of pore pressure on fluid migration is dominant.Therefore,the permeability increases with increasing pore pressure.When the initial permeability is relatively low,the pore pressure may have a dominant role in promoting fluid migration for the fluid with weak adsorption capacity.However,for the fluid with strong adsorption capacity,the adsorption strain caused by pore pressure may play a leading role,and the permeability reduces first and then ascends with increasing pore pressure.
文摘Coal fly ash （CFA） generated by coal-based thermal power plants is mainly composed of some oxides having high crystallinity, including quartz and mullite. In this study, the effect of CFA crystallinity toward its capacity on Pb（Ⅱ） adsorption was investigated. CFA with various crystaUinity was obtanied by refluxing it with sodium hydroxide （NaOH） solution having various concentrations （1-7 M） at various temperature and reflux time. To evaluate the effect of crystallinity of treated CFA on the adsorption capacity, adsorption of Pb（Ⅱ） solution with treated CFA was carried out. The research shows that the reflux of CFA with NaOH solution leads to the crystallinity of quartz and mullite in CFA decreased. The decrease is proportional with the concentration increasing, the temperature elevation, and the longer time. The reflux using NaOH solution with high concentration （〉 3 M） in addition causes a decrease in the crystallinity of quartz and mullite, also results in the formation of hydroxysodalite. The decrease of the CFA crystalllinity gives an increase in CFA adsorption capacity toward Pb（Ⅱ） solution.
文摘The static adsorption performances of a series of active carbon fiber(ACF)for xenon at 201 K were measured with a model ASAP2010M specific surface area and aperture distribution instrument by changing the working gas of instrument from N 2 to Xenon. Compared with grain active carbon(GAC): (1) the adsorption performance of Viscose based ACF(VACF) adsorbents is better than that of GAC; (2) owing to the difference of aperture distribution, the adsorption performance of ACF with different radicales is different under the same experiment conditions though the specific surface area is similar; (3) there is no definite relationship between adsorption performance and specific surface area; (4) the VACF A2 is the superior xenon adsorbent at the experimental temperature.
基金the supports of the Na-tional Natural Science Foundation of China(No.U19B2007,42072202)the China Postdoctoral Science Foundation(No.2025MD774057)。
文摘Organic matter(OM)is the primary gas occurrence carrier in shale reservoirs due to their abundant nanopores.To reveal the OM pore structure,adsorption capacity and evolution during thermal maturation,this study collected data from samples spanning the entire evolution stage,from immature to over-mature.Scanning Electron Microscope(SEM)observation and low temperature gases adsorption experiments were used to qualitatively-semi-quantitatively and quantitatively analyze OM pore structure evolution,and CH_(4) isothermal adsorption experiments were used to reveal the adsorption capacity evolution.Then,the influence and mechanism of matu rity and hydrocarbon generation on pore development and adsorption capacity were quantitatively reviewed based on the experimental data.The results show that OM pores are poorly developed in the immature stage due to weak hydrocarbon generation,although micro-fractures are occasionally found at the edges of OM particles.In the low maturity stage,OM pores are partially developed due to liquid hydrocarbon generation,with liquid hydrocarbons also filling some OM pores.The contribution of total organic carbon content(TOC)to adsorption extent is not significant in these two stages.From high to high-over maturity stages,massive gaseous hydrocarbons are generated,significantly improving the surface porosity of OM.Clear positive linear correlations are observed between TOC and adsorption amount.However,the development of OM pores significantly declines when thermal maturity(R_(o))exceeds 3.5%due to excessive aromatization.The accuracy of research on the evolution of pore structure and adsorption capacity is limited by several factors:(ⅰ)errors caused by sample specification,calculation processes,parameter settings,and kerogen models in isothermal adsorption experiments and molecular simulations;(ⅱ)difficulty in achieving control variables due to the strong heterogeneity of natural maturation shale samples;and(ⅲ)the need to enhance compatibility between thermal simulation experiments and natural thermal evolution.Therefore,isothermal adsorption experiments on bulk shale and molecular simulations of intact shale model are necessary,taking into account the dynamic temperature and pressure of in-situ reservoirs.Moreover,shale samples with varying maturity,influenced by their distance from the paleo-thermal source,may provide significant verification for thermal simulation experiments.
文摘The purpose of this research work is to determine the removal efficiency of Cu^(2+)and Pb^(2+)ions using polyvinyl alcohol/neem leaf extract/chitosan(PVA/NLE/CS)composite films as adsorbent materials from an aqueous medium,with respect to pH,contact time,and adsorbent dosage.The synthesized composite material was characterized using Fourier Transform Infrared(FTIR)spectroscopy,thermogravimetric analysis-Derivative Thermogravimetry(TGA-DTG),X-ray diffraction(XRD),X-ray photoelectron spectroscopy(XPS),and scanning electron microscopy-Energy Dispersive X-ray Spectroscopy(SEM-EDX).The antibacterial activity and swelling response of the material were studied using suitable methodologies.The FTIR study confirmed the interactions among PVA,chitosan,and neem leaf extract.The TGA data reveal the excellent thermal stability of the developed composite films.The SEM micrograph indicates a homogeneous phase morphology with good compatibility among chitosan,the monomer,and the leaf extract.The antibacterial study revealed that the prepared PVA/NLE/CS films exhibit improved antibacterial activity against bacterial growth.It was found that at pH 6.0,the adsorption capacity for both toxic metal ions is maximum,and decreases with a further rise in pH.At this pH,the adsorption capacity of PVA/NLE/CS films increases with a gradual increase in adsorbent dosage,and at a specific pH,the adsorption capacity for Cu^(2+)is greater than that for Pb^(2+).The adsorption efficiency is a function of contact time and was found to be maximal at 180 min.Hence,the developed composite material is effective for the removal of metal ions from wastewater.
基金Project (50774100) supported by the National Natural Science Foundation of China
文摘A novel adsorbent was prepared by modifying orange peel with sodium hydroxide and calcium chloride. The morphological and characteristics of the adsorbent were evaluated by infrared spectroscopy （IR）, scanning electron microscopy （SEM） and N2-adsorption techniques. The adsorption behavior of Cu^2＋, Pb^2＋ and Zn^2＋ on modified orange peel （SCOP） was studied by varying parameters like pH, initial concentration of metal ions. Equilibrium was well described by Langmuir equation with the maximum adsorption capacities for Cu^2＋, Pb^2＋ and Zn^2＋ of 70.73, 209.8 and 56.18 mg/g, respectively. Based on the results obtained in batch experiments, breakthrough profiles were examined using a column packed with SCOP for the separation of small concentration of Pb^2＋ from an excess of Zn^2＋ followed by elution tests. Ion exchange with Ca^2＋ neutralizing the carboxyl groups of the pectin was found to be the predominant mechanism.
基金the National Natural Science Foundation of China(Grant Nos.42141012,41972168,and 42030810)the Peng Cheng Shang Xue Education Fund of CUMT Education Development Foundation(No.PCSX202204)+1 种基金the Fundamental Research Funds for the Central Universities(No.2020ZDPYZD01)aa project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions.
文摘CCUS (carbon capture, utilization, and storage) technology is regarded as a bottom method to achieve carbon neutrality globally. CO_(2) storage in deep coal reservoirs serves as a feasible selection for CCUS, and its storage potential can be attributed to the CO_(2) adsorption capacity of the coal. In this paper, a series of CO_(2) adsorption isotherm experiments were performed at different pressures and temperatures in sub-bituminous coal from the southern Junggar Basin (reservoir temperature ∼25.9°C and pressure ∼3.91 MPa). In addition, the high-pressure CO_(2) adsorption characteristics of the southern Junggar Basin coal were characterized using a supercritical D-R adsorption model. Finally, the CO_(2) storage capacities in sub-bituminous coal under the in situ reservoir temperature and pressure were analyzed. Results indicated that the excess adsorption capacities increase gradually with increasing injection pressure before reaching an asymptotic maximum magnitude of ∼34.55 cm3/g. The supercritical D-R adsorption model is suitable for characterizing the excess/absolute CO_(2) adsorption capacity, as shown by the high correlation coefficients > 0.99. The CO_(2) adsorption capacity increases with declining temperature, indicating a negative effect of temperature on CO_(2) geological sequestration. By analyzing the statistical relationships of the D-R adsorption fitting parameters with the reservoir temperature, a CO_(2) adsorption capacity evolution model was established, which can be further used for predicting CO_(2) sequestration potential at in situ reservoir conditions. CO_(2) adsorption capacity slowly increases before reaching the critical CO_(2) density, following a rapid decrease at depths greater than ∼800 m in the southern Junngar Basin. The research results presented in this paper can provide guidance for evaluating CO_(2) storage potential in deep coal seams.
基金supported by the National Natural Science Foundation of China(Grant No.41972160)Open fund of Key Laboratory of oil and gas resources research,Chinese Academy of Sciences(KLOR2018-7).
文摘Determination of gas adsorption capacity under geological conditions is essential in evaluating shale gas resource potential.A quantitative determination of gas adsorption capacity was proposed through 1)investigating controlling geological factors(including both internal ones and external ones)of gas adsorption capacity in organic-rich marine shale with geochemical analysis,XRD diffraction,field-emission scanning electron microscopy,and methane sorption isotherms;2)defining the relationship between gas adsorption capacity and single controlling factor;3)establishing a comprehensive determination model with the consideration of all these controlling factors.The primary controlling factors of the sorption capacity for the studied O3wLower S1l shale are TOC,illite and quartz,temperature,pressure,Ro,and moisture(water saturation).Specifically,TOC,thermal maturity,illite,and pressure are positively correlated with sorption capacity,whereas,quartz and temperature contribute negatively to the sorption capacity.We present the quantitative model along with application examples from the Wufeng-Lower Longmaxi Shale in the southeast Sichuan Basin,west China,to demonstrate the approach in shale gas evaluation.The result shows that the comprehensive determination model provides a good and unbiased estimate of gas adsorption capacities with a high correlation coefficient(0.96)and bell-shaped residues centered at zero.
文摘The goal of this work is to improve the simultaneous removal of Pb2+, Cu2+, Zn2+, and Cd2+ ions from synthetic wastewater in a fixed bed column by incorporating sodium dodecyl sulfate (SDS) onto the surface of activated carbon made from coconut shells. The activated carbons were characterized using Fourier transform infrared spectroscopy (FT-IR) and scanning electron microscopy-energy dispersive x-ray (SEM-EDX). The adsorption column dynamics were studied by varying the flow rates (5, 10 and 15 mL/min), bed heights (10, 15 and 20 cm), and initial concentrations (50, 150, and 250 mg/L). The activated carbon has a pore volume of 0.715 cm3/g and a BET-specific surface area of 1410 m2/g. Sodium dodecyl sulfate (SDS) surfactant incorporation onto the surface of the activated carbon enhances its capacity for simultaneous adsorption of Pb2+, Cu2+, Zn2+, and Cd2+ from the aqueous medium. The affinity of the heavy metals to both unmodified (AC) and modified (AC-SDS) activated carbons followed the order of Pb2+ > Cu2+ > Zn2+ > Cd2+. The dynamic adsorption of the column depends on the flow rate, bed height, initial metal concentration, and SDS surface modification. With a 5 mL/min flow rate, a 20 cm bed height, and a 50 mg/L initial metal concentration, a maximum break-through time of 150 minutes for the unmodified activated carbon (AC) and 180 minutes for the SDS-modified activated carbon (AC-SDS) was reached.
文摘Increased human and industrial activities have exacerbated the release of toxic materials and acute envi-ronmental pollution in recent times.Biochar,a carbon-rich material produced from biomass,is gaining momentum as a versatile material for attaining a sustainable environment.The study reviews the application of functionalized biochar for energy storage,environmental remediation,catalysis,and sustainable agriculture,aiming to achieve a greener future.Thedeployment of crop residues as a renewable feedstock for biochar,and their properties,compositions,modification,and functionalization techniques are also discussed.Additionally,the avenues for applying functionalized biochar to achieve a greener future,future trends and innovations,challenges,and future research directions are highlighted.Despite the limitations of scalability,ecotoxicological risks,logistical issues,lack of characterization protocols,high production costs,poor social acceptance,and inadequate policy and regulatory frameworks,functionalized biochar offers a better surface area,improved porosity,enhanced functional groups,and higher recoverability,leading to improved performance,adsorption capacity,biodegradability,and applications in specialized fields.Future research should prioritize standardization,scalability,cost reduction strategies,expansion of application areas,integration of emerging tools such as artificial intelligence and predictive modeling,and the development of policy and regulatory frameworks,ensuring that biochar’s full potential is harnessed effectively to support a low-carbon,resource-efficient future and global sustainability goals.
文摘Aluminum hydroxide adjuvant exhibits a poorly crystalline boehmite(PCB)structure,which demonstrates instability during prolonged storage.In the present study,we systematically investigated the quality alterations of the adjuvant stored at roo m temperature by analyzing its crystal structure,particle size distribution,electron microscopic characteristics,pH,isoelectric point(pI),and adsorption capacity.These assessments aimed to ensure the effectiveness and safety of vaccine production.Three batches of adjuvants were stored at room temperature for 15 months,and their changes were monitored using X-ray diffraction patterns,transmission electron microscopy(TEM),pH measurements,pI determination,and adsorption capacity analysis.X-ray diffraction revealed that the crystalline phases of aluminum hydroxide initially exhibited a PCB structure,which became progressively more ordered during storage.Notably,after 12 months,a new diffraction peak emerged at 18.2°2θ,with its intensity increasing over time.This corresponded to the formation of highly crystalline gibbsite and bayerite,which compromised the stability of the adjuvant.Furthermore,the pH and pI values decreased during storage,reflecting a decline in the chemical stability of the adjuvant.Comprising nanoparticles with a mean diameter of 130 nm,the adjuvant maintained a high surface area and excellent adsorption capacity.The adsorption rate at 8 mg BSA/mg Al3+consistently exceeded 97%,with no statistically significant differences observed between the adsorption capacities at 1 and 15 months(P>0.05).This indicated that the nanoparticle aluminum hydroxide adjuvant sustained high adsorption efficiency throughout the storage period,underscoring its reliability as a vaccine adsorbent.However,in the later stages of storage,the emergence of highly crystalline gibbsite and bayerite,coupled with declines in pH and pI,negatively impacted the adjuvant’s stability.Based on these findings,we recommended that aluminum hydroxide adjuvants should not be stored at room temperature for longer than 12 months to preserve their quality and efficacy.
文摘The aluminum hydroxide adjuvant possesses a poorly crystalline boehmite (PCB) structure, the stability of which is significantly affected by storage conditions. In the present study, we conducted a comprehensive investigation into the structural and quality alterations of aluminum hydroxide adjuvants under varying temperature conditions over time. Three batches of the adjuvant were stored at 2–8℃, 18–25℃, and 37℃, respectively, for 6 months. Key parameters, including X-ray diffraction patterns, pH, isoelectric point (pI), adsorption capacity, and average particle size, were analyzed to assess the impact of storage temperatures. X-ray diffraction analysis confirmed the PCB structure of the aluminum hydroxide adjuvant. Notably, after 1 month of storage at 37℃, new diffraction peaks emerged at 18.2 °2θ, with their intensity increasing progressively over time. Concurrently, the largest decreases in pI and pH were observed, measuring 0.78 and 1.33, respectively. In contrast, adjuvants stored at 2–8℃ for 6 months exhibited only faint diffraction peaks at 18.2 °2θ, indicating minor structural changes. Under these conditions, the reductions in pI and pH were comparatively smaller, at 0.43 and 0.80, respectively. The average particle size of the adjuvants remained within 110–140 nm across all storage conditions. Additionally, the aluminum hydroxide adjuvant consistently demonstrated a high protein adsorption capacity, approximately 8 mg BSA/mg Al^(3+), with no statistically significant differences in adsorption rates observed among the different temperature conditions (P > 0.05). These findings highlighted the remarkable adsorption efficiency of nanoparticle aluminum hydroxide adjuvants throughout storage, reinforcing their potential as superior vaccine adsorbents. However, elevated storage temperatures were shown to accelerate structural aging, promoting the formation of highly crystalline phases such as gibbsite or bayerite, which could compromise the stability and quality of the adjuvant.
基金financially supported by the National Key Research and Development Program of China(2022YFE0206300)the National Natural Science Foundation of China(U21A2081,22075074,22209047)+4 种基金the National College Students Innovation and Entrepreneurship Training Program(S202410532594,S202410532357)the Macao Science and Technology Development Fund(File No.0013/2021/AMJ)the Foundation of Yuelushan Center for Industrial Innovation(2023YCII0119)JST SICORP(JPMJSC2112)JST PRESTO(JPMJPR23QA)。
文摘Controlling surface chemistry is critically important for improving the initial Coulombic efficiency(ICE)and adsorption capacity of hard carbon anode used in Li/Na/K-ion batteries.However,accurately identifying the types and concentrations of hydrogen/oxygen terminated functional groups(HTFG/OTFGs)and distinguishing their functionalities remain challenge.Herein,we quantitatively investigated the surface chemistry on hard carbon via ultra-high temperature programed desorption measurements,and uncovered the role of HTFG/OTFGs in influencing ICE and adsorption capacity in Li/Na/K-ions cells.The C-H group is found to be dominant species on the surface of hard carbon,and presents a positive correlation with ICE values and adsorption capacity.The low reactivity of C-H group with both electrolyte salt and solvent results in the formation of thinner and highly conducive solid electrolyte interphase(SEI)layer,which benefit for the enhanced ICE and improved Li/Na/K-ions diffusion across SEI layer.Additionally,the pimping trapping effect of C-H groups allows the adsorbed Li/Na/K-ions to migrate into graphitic interlayer quickly,enhancing the slope capacity.By fabricating a C-H group-rich surface chemistry on hard carbon,a high ICE value and satisfactory specific capacity have been realized.These findings enrich our understanding of the surface chemistry-induced interfacial reaction,which effectively guides the rational design of high-performance hard carbon.
文摘Wastewater plays a crucial role in deteriorating water quality and can significantly affect human health and ecosystems if discharged without proper treatment.Among available treatment methods,adsorption is often considered an effective,relatively inexpensive,and environmentally friendly purification technique,but its efficiency depends on the sorbents used.The use of low-cost biosorbents with high adsorption capacity is widely studied.These include various biomaterials such as microalgae,cyanobacteria,fungi,and plant materials.The utilization of different biosorbents derived from plant waste,such as Paulownia wood,aspen,hickory,Ziziphus bark,peach tree shavings,as well as grasses such as red fescue and reed,and Sargassum algae in natural and modified forms,is a crucial research direction.Such studies highlight the potential to address waste issues by repurposing it as biosorbents.Several studies have examined the ability of different biosorbents to treat wastewater and suggested that the physicochemical properties of the material's surface,such as specific surface area,pore size,and pore volume,play a decisive role in adsorption capacity.A quantitative analysis of plant-based biosorbents will significantly aid in developing water treatment systems and achieving optimal adsorption through modifications of their physicochemical properties.Furthermore,the analysis will help understand the relative importance of each physicochemical property in determining adsorption capacity,thereby contributing to the implementation of treatment methods targeting specific pollutants.
基金supported by the National Major Science and Technology Project"Key Technologies for Exploration and Development of Continental Shale Gas in Yan'an"(No.2017ZX05039001005).
文摘In order to improve the calculation method of the isosteric adsorption heat,clarify thermodynamic characteristics of CH4 adsorption by continental shale and reveal the adsorption mechanism,this paper selected shale samples from the seventh Member of Yanchang Formation of Upper Triassic in the Yanchang Gasfield of the Ordos Basin as the research object.The isothermal adsorption experiment was carried out on the CH4 adsorption by continental shale and the excess adsorption curves were plotted.Then,the characteristics of the isosteric adsorption heat of the shale with different types of adsorption capacity were illustrated by analyzing and comparing the difference between excess and absolute adsorption capacity.And the following research results were obtained.First,under the same temperature and pressure,absolute adsorption capacity is higher than the excess values.The difference between them is higher under low temperature and high pressure and it is in the relationship of exponential function with the equilibrium pressure.If excess adsorption capacity is used to evaluate the adsorptive property of shale reservoirs,the evaluation result will be underestimated.Second,for CH4 adsorption by Yanchang Formation shale,the absolute and excess isosteric adsorption heat values have a linear positive correlation with absolute and excess adsorption capacity respectively,and the intermo-lecular force of adsorbate has a dominant effect on isosteric adsorption heat values.Third,absolute isosteric adsorption heat value is less than the excess heat.The relative error is in the range of 18.18e49.79%,and it is higher in the stage with low adsorption capacity.If excess adsorption capacity is taken as the basic data to calculate initial isosteric adsorption heat values,the calculation result will be overvalued,and consequently,the evaluation of the intermolecular force of adsorbent and adsorbate is overestimated.
基金Supported by the National Natural Science Foundation of China (Nos. 40871110 and 30828005)the National Water Pollution Control and Management Special Project of China (No. 2009ZX07102-003)+1 种基金the Special Project of Science and Technology of Guangdong Province,China (No. 2008A080800028)the Supporting Project of Science and Technology of Guangzhou City,China (No. 2008Z1-E621)
文摘Constructed wetlands （CWs） are engineered systems that utilize natural systems including wetland vegetations, soils, and their associated microbial assemblages to assist in treating wastewater. The kinetic adsorption of ammonium nitrogen （NH＋-N） by CW substrate materials such as blast furnace slag （BFS）, zeolite, ceramsite, vermiculite, gravel, paddy soil, red soil, and turf, was investigated using batch experiments and kinetic adsorption isotherms. Both Freundlich and Lang- muir isotherms could adequately predict the NH＋-N adsorption process. The maximum adsorption capacities of NH＋-N, estimated from the Langmuir isotherm, ranked as： zeolite （33 333.33 mg kg^-1） 〉 turf （29274.01 mg kg^-1） 〉 BFS （5000 mg kg^-1） 〉 vermiculite （3333.33 mg kg^-1） 〉 gravel （769.23 mg kg^-1） 〉 paddy soil （588.24 mg kg^-1） 〉 red soil （555.56 mg kg^-1） 〉 ceramsite （107.53 mg kg^-1）. Some properties of the substrate materials, including bulk density, specific gravity, hydraulic conductivity, uniformity coefficient （K60）, curvature coefficient （Co）, organic matter, pH, exchangeable （or active） Cu, Fe, Zn and Mn, total Cu, and Fe, Mn, Zn, Cd, Pb and Ca, had negative correlations with NH＋-N adsorption. Other properties of the substrate materials like particle diameter values of D10, 030 and 060 （the diameters of particle sizes of a substrate material at which 10%, 30% and 60%, respectively, of the particles pass through the sieve based on the accumulative frequency）, cation exchange capacity （CEC）, exchangeable （or active） Ca and Mg, and total K and Mg had positive correlations with NH＋-N adsorption. In addition, active K and Na as well as the total Na had significant positive correlations with NH＋-N adsorption. This information would be useful for selection of suitable substrate materials for CWs.
基金supported by the United Fund Project of National Natural Science Foundation of China (Grant No. U1262209)the National Natural Science Foundation of China (Grant No. 41602155)the Young Scholars Development Fund of SWPU (No. 201599010137)
文摘In this paper, the methane adsorption behaviours in slit-like chlorite nanopores were investigated using the grand canonical Monte Carlo simulation method, and the influences of the pore sizes, temperatures, water, and compositions on methane adsorption on chlorite were discussed. Our investigation revealed that the isosteric heat of adsorption of methane in slit-like chlorite nanopores decreased with an increase in pore size and was less than 42 kJ/mol, suggesting that methane adsorbed on chlorite through physical adsorption. The methane excess adsorp- tion capacity increased with the increase in the pore size in micropores and decreased with the increase in the pore size in mesopores. The methane excess adsorption capacity in chlorite pores increased with an increase in pressure or decrease in pore size. With an increase in temperature, the isosteric heats of adsorption of methane decreased and the methane adsorption sites on chlorite changed from lower- energy adsorption sites to higher-energy sites, leading to the reduction in the methane excess adsorption capacity. Water molecules in chlorite pores occupied the pore wall in a directional manner, which may be related to the van der Waals and Coulomb force interactions and the hydrogen bonding interaction. It was also found that water molecules existed as aggregates. With increasing water content, the water molecules occupied the adsorption sites and adsorption space of the methane, leading to a reduction in the methane excess adsorption capacity. The excess adsorption capacity of gas on chlorite decreased in the following order： carbon dioxide 〉 methane 〉 nitrogen. If the mole fraction of nitrogen or carbon dioxide in the binary gas mixture increased, the mole fraction of methane decreased, methane adsorption sites changed, and methane adsorption space was reduced, resulting in the decrease in the methane excess adsorption capacity.
文摘A semi-empirical adsorption kinetic model was proposed with the time compensation method to describe the chemisorption of SO2 in flue gas by carbon adsorbents for flue gas purification.The change in adsorption capacity and adsorption rate with time at different water vapor concentrations and different SO2 concentrations was studied.The model was in good agreement with experimental data.The surface reaction was probably the rate controlling step in the early stage for SO2 adsorption by ZL50 activated carbon.The parameters m and n in the nth order adsorption kinetic model were related to the magnitude of the time compensation and adsorption driving force,respectively.The change of parameter n with water vapor concentrations and sulfur dioxide concentrations was studied and some physical implications were given.The sum of square errors was less than 1.0 and the average absolute percentage deviations ranged from 0.5 to 3.2.The kinetic model was compared with other models in the literature.
