An analytical transient coal permeability model:Sorption non-equilibrium index-based swelling switch

Long-term permeability experiments have indicated that sorption-induced swelling can switch from internal to bulk depending on the evolutive sorption status.However,this sorption swelling switch mechanism has not been considered in current analytical permeability models.This study introduces a normalized sorption non-equilibrium index(SNEI)to characterize the sorption status,quantify the dynamical variations of matrix swelling accumulation and internal swelling partition,and formulate the sorption swelling switch model.The incorporation of this index into the extended total effective stress concept leads to an analytical transient coal permeability model.Model results show that the sorption swelling switch itself results in the permeability switch under stress-constrained conditions,while the confined bulk swelling suppresses the permeability recovery to the continuous reduction under displacement-constrained conditions.Model verifications show that current experimental observations correspond to the early stages of the transient process,and they could be extended to the whole process with these models.This study demonstrates the importance of the sorption swelling switch in determining permeability evolution using simple boundary conditions.It provides new insights into experimentally revealing the sorption swelling switch in the future,and underscores the requirement of a rigorous model for complex coupled processes in large-scale coal seams.

Analysis of CH_(4) and H_(2) Adsorption on Heterogeneous Shale Surfaces Using aMolecular Dynamics Approach

Determining the adsorption of shale gas on complex surfaces remains a challenge in molecular simulation studies.Difficulties essentially stem from the need to create a realistic shale structure model in terms of mineral heterogeneityand multiplicity.Moreover,precise characterization of the competitive adsorption of hydrogen andmethane in shale generally requires the experimental determination of the related adsorptive capacity.In thisstudy,the adsorption of adsorbates,methane(CH_(4)),and hydrogen(H_(2))on heterogeneous shale surface modelsof Kaolinite,Orthoclase,Muscovite,Mica,C_(60),and Butane has been simulated in the frame of a moleculardynamic’s numerical technique.The results show that these behaviors are influenced by pressure and potentialenergy.On increasing the pressure from 500 to 2000 psi,the sorption effect for CH_(4)significantly increasesbut shows a decline at a certain stage(if compared to H_(2)).The research findings also indicate that raw shalehas a higher capacity to adsorb CH_(4)compared to hydrogen.However,in shale,this difference is negligible.

The Al_(2)O_(3)and Mn/Al_(2)O_(3)sorbents highly utilized in destructive sorption of NF_(3)

NF_(3)is commonly used as an etching and cleaning gas in semiconductor industry,however it is a strongly greenhouse gas.Therefore,the destruction of disposal NF_(3)is an urgent task to migrate the greenhouse effect.Among the technologies for NF_(3)abatement,the destructive sorption of NF_(3)over metal oxides sorbents is an effective way.Thus,the search for a highly reactive and utilized sorbent for NF_(3)destruction is in great demand.In this work,AlOOH supported on carbon-sphere(AlOOH/CS)as precursors were synthesized hydrothermally and heat-treated to prepare the Al_(2)O_(3)sorbents.The influence of AlOOH/CS hydrothermal temperatures on the reactivity of derived Al_(2)O_(3)sorbents for NF_(3)destruction was investigated,and it is shown that the Al2O3 from AlOOH/CS hydro-thermalized at 120℃is superior to others.Subsequently,the optimized Al_(2)O_(3)was covered by Mn(OH)x to prepare Mn/Al_(2)O_(3)sorbents via changing hydrothermal temperatures and Mn loadings.The results show that the Mn/Al_(2)O_(3)sorbents are more utilized than bare Al_(2)O_(3)in NF_(3)destructive sorption due to the promotional effect of Mn_(2)O_(3)as surface layer on the fluorination of Al_(2)O_(3)as substrate,especially the optimal 5%Mn/Al2O3(160℃)exhibits a utilization percentage as high as 90.4%,and remarkably exceeds all the sorbents reported so far.These findings are beneficial to develop more efficient sorbents for the destruction of NF_(3).

Enhanced and irreversible sorption of pesticide pyrimethanil by soil amended with biochars

Biochar derived from partial combustion of vegetation is ubiquitous and potentially effective in sequestration of environmental contaminants. Biochars were prepared by burning of red gum （Eucalyptus spp.） woodchips at 450 and 850℃ （labeled as BC450 and BC850）. These two biochars were found to possess markedly different properties in terms of surface area and porosity. Short-term equilibration tests （24 hr） were conducted to assess the sorption-desorption behavior of pyrimethanil in the soil amended with various amounts of biochar of each type, with a special focus on the desorption behavior of the sorbed pesticide through four times successive desorption by dilution. Sorption coefficient and isotherm nonlinearity of the amended soils progressively increased with the content of biochar in the soil. Biochar BC850 with higher surface area and microporosity showed a stronger effect on the reversibility of sorption pesticide. The soils amended with 5% BC450 and 1% BC850 had nearly the same sorption capacity for pyrimethanil; however, their desorption processes were very different with 13.65% and 1.49% of the sorbed pesticide being released, respectively. This study suggested that biochar in soil could be an important factor for immobilization of a pesticide and thus affecting its environment fate in soil.

Effect of temperature on the sorption and desorption of perfluorooctane sulfonate on humic acid

Sorption and desorption of perfluorooctane sulfonate （PFOS） on humic acid at different temperatures were studied. It was found that the sorption process could be modeled with power kinetic equation very well, suggesting that diflusion predominated the sorption of PFOS on the humic acid. The sorption capacity was doubled when the temperature increased from 5 to 35°C, and thermodynamics parameters △G0 was calculated to be –7.11 to –5.04 kJ/mol, △H0 was 14.2 kJ/mol, and △S 0 was 69.5 J/（mol·K）, indicating that the sorption was a spontaneous, endothermic, and entropy driven process. Desorption hysteresis occurred at all studied temperatures which suggested that humic acid may be an important sink of PFOS in the environment.

Batch studies of adsorption of copper and lead on activated carbon from Eucalyptus camaldulensis Dehn. bark

Powdered activated carbon (PAC) prepared from Eucalyptus camaldulensis Dehn. bark was tested for its adsorption capacity for Cu(Ⅱ) and Pb(Ⅱ). The experiment was conducted to investigate the effects of pH, contact time, initial metal concentration, and temperature. The best adsorption of both Cu(Ⅱ) and Pb(Ⅱ) occurred at pH 5, where the adsorption reached equilibrium within 45 min for the whole range of initial heavy metal concentrations (0.1-10 mmol/L). The adsorption kinetics was found to follow the pseudo-...

Numerical modeling of radionuclide migration in porous media with nonequilibrium sorption

When radionuclides migrate in porous media with water serving as carrier, the mechanism of sorption and desorption is not negligible. nonequilibrium conditions exist in sorption and desorption. In this paper,a numerical model of radionuclide migration with nonequilibrium sorption was developed.The algorithm of numerical descretizing and direct substituting was adopted in coupling of the convective-dispersive equation and the nonequilibrium sorption isotherm in this model ,and this makes it easier to solve the model numerically.A quantitative analysis is made for the first time that the influence of nonequilibrium sorption, represented by the rate coefficient which shows how quickly the nonequilibrium condition in sorption and desorption reaches equilibrium on the migration of radionuclide,and results show that it affects the migration perceptibly. Finally the model was verified by using the observed data of radionuclide migration test conducted in the field, and which clarified its availability.

Equilibrium and kinetics of copper(Ⅱ) biosorption by Myriophyllum spicatum L.

The potential use of Myriophyllum spicatum L. biomass as a biosorbent for the removal of copper（ Ⅱ ） from aqueous solution was investigated in laboratory condition. The sorption experiments were undertaken to obtain copper（ Ⅱ ） biosorption properties of M. spicatum L., i.e. equilibrium time, the maximum capacity, and rate constants. Copper（ Ⅱ ） biosorption was fast and equilibrium was attained within 35 min at initial copper（ Ⅱ ） concentration of 6 mg/L. Different isotherm models including the Langmuir, Freundlich, Temkin and Redlich-Peterson model, were used to investigate the sorption capacity and isotherm. These models showed an excellent match with the experimental data except for the Freundlich model. According to the Langmuir coefficients, the maximum sorption capacity of copper onto M. spicatum L. was 10.80 mg/g. The kinetics of copper（ Ⅱ ） sorption was also analysed and rate constants were derived. It was found that the overall sorption process was best described by the pseudo second-order equation, and that intraparticle diffusion was not the rate determining step. The results of this study showed that M. spicatum L. can be considered as useful vehicles for the removal and recovery of copper（ Ⅱ ） from aqueous solutions.

Effects of Pb^(2+), Cd^(2+) and Cu^(2+) on the Aqueous Zn^(2+) Sorption by Hydroxyapatite

In this paper, the behaviors of aqueous zinc sorption by hydroxyapatite in the co-existence of Pb^2＋, Cd^2＋ and Cu^2＋ are investigated, the effects of Pb^2＋, Cd^2＋ and Cu^2＋ on the sorption of Zn^2＋ are discussed, and the hydroxyapatite sorption capabilities for Pb^2＋, Cd^2＋, Cu^2＋ and Zn^2＋ are compared. The experimental results show that the Zn^2＋ removal efficiency decreases gradually with the increase of the Cd^2＋ concentration of the solution, and there is no sorption preference between Cd^2＋ and Zn^2＋. On the other hand, the Zn^2＋ removal efficiency rapidly decreases rapidly with the increase of the Cu^2＋ concentration of the solution, and there is a clear sorption preference between Cu^2＋ and Zn^2＋. It is noticed that the Zn^2＋ removal efficiency is hardly changed with the variance of Pb^2＋ concentration because the removal mechanisms for these two ions are totally different. It is concluded that the adsorption affinities of the heavy metals for the hydroxyapatite follows this sequence： pb^2＋〉 Cu^2＋〉 Cd^2＋〉 Zn^2＋.

Sorption Behaviours of Exfoliated Graphite

Exfoliated graphite (EG) is selected as a new kind of sorbent to sorb heavy oil spilled. In order to make use of EG more effectively, some basic experiments are performed to investigate its sorption properties, i.e. , specific sorption, height of saturation layer, sorption time constant. In the present experiments, A grade heavy oil is employed as a standard sorbate. It is concluded that 1) under the condition that the area of solid (filter bottom) liquid (heavy oil) interface is a constant, specific sorption usually decreases when the amount of EG filled or the apparent bulk density increase; however, the specific sorption initially increases when the apparent bulk density is too low and the amount of EG filled is too much; 2) under the condition that the apparent bulk density of EG filled is a constant, the sorption time constant tends to increase when the amount of EG filled increases; however, for a constant amount of EG filled, the sorption time constant will decrease when the apparent bulk density increases.

Adsorption Characterization of Strontium on PAN/Zeolite Composite Adsorbent

This work reports the adsorption of strontium from aqueous solutions onto PAN/zeolite composite. The strontium adsorption on the composite adsorbent was studied as a function of initial strontium concentration, pH of the solution, contact time and temperature. Adsorption isotherms like Langmuir, Freundlich,Dubinin–Radushkevich (D–R) and Temkin were used to analyze the equilibrium data at the different concentrations.Adsorption process well fitted to Temkin isotherm model. Thermodynamic parameters such as the changes in enthalpy, entropy and Gibbs’ free energy were determined, showing adsorption to be an exothermic and spontaneous process.

Preparation and water sorption properties of novel SiO_(2)-LiBr microcapsules for water-retaining pavement

Novel SiO_(2)-LiBr microcapsules for water-retaining pavement were prepared and firstly characterized by scanning electron microscope(SEM),particle size analysis,and Fourier transform infrared spectroscopy(FT-IR).The water vapor sorption and desorption of the formulated microcapsules was then experimentally studied using dynamic vapor sorption(DVS),with the results fitted to three kinds of adsorption kinetics models.In addition,the specific surface area(SSA)was also calculated based on BET theory;and the thermal performance was investigated by laser flash analysis(LFA).Experimental results show a change of 103%in mass of the microcapsule sample under 90%relative humidity(RH)at 30℃after water vapor sorption.The fitting of results indicates that the adsorption process is mainly governed by the intra-particle diffusion mechanism,followed by the pseudo-first-order adsorption process.In comparison with most conventional pavement materials,it is found that the SSA of the formulated microcapsules is much larger while the thermal conductivity is lower.The unique properties of the formulated SiO_(2)-LiBr microcapsules have significant potential to take the edge off the urban heat island effect and reduce rutting when applied to water-retaining pavement materials.

Sorption equilibrium moisture and isosteric heat of Chinese wheat bran products added to rice to increase its dietary fibre content

More and more people concern about supplementing dietary food with wheat bran to increase fibre content,but there has been little study of the sorption isotherms and isosteric heats of wheat bran fibre products,which are important to the quality and storage durability of such commodities.This study collected equilibrium moisture content(EMC)and equilibrium relative humidity(ERH)data on six Chinese wheat bran products via the static gravimetric method and analysed their sorption isosteric heats.Results showed that all six wheat bran products had sigmoidal isotherms.The data were best fitted by polynomial,modified GAB,modified Oswin,and modified Halsey models.The relative safe moisture contents of the six wheat bran products were 12.20%–13.86%wet basis(w.b.).The heat of vaporization of wheat bran products approached the latent heat of pure water at around a moisture content(MC)of 22.5%and approximately 2450 kJ/kg.A process of extrusion and ultrafine grinding reduced the solid surface area and sorption isosteric heats of the monolayer,multilayer and condensed water regions in the wheat bran products.In the temperature range of 10–37℃,the EMC of sorption in monolayer,multilayer and condensed water regions decreased with increasing temperature.The milled rice to which 1%–3%200-mesh wheat bran product was added maintained its texture when made into cooked rice and its thermomechanical properties when made into rice dough.After processing by extrusion and ultrafine grinding,wheat bran products have a lower solid surface area and lower monolayer water content(Mm)and sorption isosteric heat values.Some 3%200-mesh wheat bran product can be added to cooked rice for increasing its fibre content and making it more nutritious.

Sorption Separation of Pairs of Elements with Similar Properties Pd(Ⅱ)-Pt(Ⅳ) and Pd(Ⅱ)-Cu(Ⅱ) Using Chemically Modified Silica Containing Sulfide Sulfur

The adsorption of Pd(Ⅱ), Pt(IV) and Cu(Ⅱ) in static and dynamic conditions on chemically modified silica containing sulfide sulfur (number of grafted functional groups of the sorbent was 0.2 (CMS-S 0.2) and 0 3 mmol/g (CMS-S 0.3)) was studied. It is established that an increase in the acidity of the sorption of Pd(Ⅱ) and Pt(Ⅳ) decreases, whereas the Cu(Ⅱ) does not change. Time to reach the constant values of the sorption is 15 min. In equal conditions, the sorption decreases in the number of Pd(Ⅱ)>Pt(IV)>Cu(Ⅱ). Based on retrieved data suggested that the sorption of Pd(Ⅱ) proceeds according the coordination mechanism. In the case of sorption from solutions with a high palladium content can be polymerization of adsorbed complexes in the sorbent phase. Worked out the optimal conditions for the separation of pairs of Pd(Ⅱ)-Pt(Ⅳ) and Pd(Ⅱ)-Cu(Ⅱ) under dynamic conditions with the extraction of palladium(Ⅱ) in the eluate is above 95%.

Sorption of Organic Compounds in Soil Organic Matter

Soil organic matter(SOM)is the predominant component for sorption of hydrophobic organic compouds in soil and sorption by SOM ultimately affects chemical fate and availability in soil,and the degree of remedia- tion success of contaminated soils. This paper summarizes the latest development on sorption of organic com- pounds in soil (natural) organic matter,addresses four sorption mechanisms: surface adsorption,solid - phase Partitioning,dual-mode sorption,and fixed-pore sorption model,and presents future research directions as well.

Preparation of Polysulfone-supported Phosphoramidic Acid Type Chelate Membrane and Its Sorption Properties for Ag^+

A blending chelate filter membrane with high chelate capacity for Ag + has been prepared by blending of phosphoramidic acid resin and polysulfone. The major parameters influencing structure of the chelate filter membranes such as the blending ratio, phosphoramidic acid resin grain size and temperature of casting solution have been studied. The relationship among the chelate amount of Ag +, pH value, Ag + concentration and phosphoramidic acid resin grain diameter were examined. The chelate filter membrane had a capacity of 1 438 μg/cm 2 for Ag + under appropriate conditions. Sorption isotherm of Ag + could be expressed with the Freundlich sorption model. The dynamic chelate experiments proved that the sorption and desorption of membranes could be realized simultaneously for Ag +.

Phosphate Desorption Characteristics of Some Representative Soils of Bangladesh: Effect of Exchangeable Anions, Water Molecules and Solution to Soil Ratios

Establishment of phosphate (P) retention and release capacity of soils is essential for effective nutrient management and environmental protection. In this experiment, we studied the influence of soil properties on P desorption and the relationship between phosphate sorption and desorption. Among the soil series, the Ghior soil had the highest percent clay (59.32%) and free iron oxide (15241 mg·kg–1) content. Along the catena of the calcareous soils, percent clay contents increased. For sorption study, the soils were equilibrated with 0.01 M CaCl2 solution containing 0, 1, 2, 4, 8, 16, 25, 50, 100 and 150 mg·P·L–1 solution. For desorption, three extractants namely, SO42- (0.005 M) as Na2SO4, HCO3- (0.01 M) as NaHCO3 and distilled water were used at extractant to soil ratios of 30:1, 60:1 and 100:1 (v/w). Among the sorption equations, the Langmuir equation showed better fit to the sorption data at higher P concentrations. The amount of phosphate desorbed by all the three extractants increased significantly with the increasing extractant to soil ratios. Phosphate desorption by and water molecules was highly correlated with pH, percent clay and free iron oxide content of the soil. Significant positive correlation (r > 0.64, P L). Phosphate desorption by SO42- and water molecules was also positively correlated with Freundlich constant, N (r > 0.67, P 0 (r > 0.72, P –0.77, P L). The results suggest that freshly sorbed phosphate ions (inner-sphere complex forming species) can be readily desobed by outer-sphere complex forming species like sulphate and bicarbonate ions. Water molecules also desorbed significant amount of freshly sorbed phosphate from the soil colloids.

Sorption and desorption behavior of lead in four different soils of India

Sorption and desorption mechanisms of lead (Pb) were determined in four different soils collected from different agro-climatic regions of India. The soils were classified as: fine loamy mixed Typic- Dystrudepts, fine sandy loam Typic Ustochrepts, fine loamy Typic Ustochrept, and fine sandy loam Udic Haplustalfs. Seven different Pb solutions [Pb(NO3)2 dissolved in 0.01M Ca(NO3)2] in a range of 400 to 2000μgL-1 were applied to study the sorption amounts at 25(±2)oC and 45(±2)oC temperatures. With the increase in application rate and tempera-ture, sorption amounts of Pb increased;however, percentages of sorption of applied Pb were decreased. Sorptions were positively and significantly (p≤0.01) correlated with Langmuir adsorption isotherm. Thermodynamic parameters of sorption (i.e. Ko, ?Go, ?Ho, and ?So) were also determined at two tempera-tures, 25(±2)oC and 45(±2)oC. Increase in Ko with the increase in temperature indicated positive effect of temperature on Pb sorption. High absolute values of ?Go, and positive values of ?Ho, and ?So suggested that the sorption reaction was spontaneous and en-dothermic. Sorbed Pb were desorbed in Pb free 0.01M Ca(NO3)2 solutions at 25(±2)oC and 45(±2)oC. Desorption amounts increased with increase in the Pb application rate, but not always with the increase in temperature.

Kinetics and Thermodynamic Studies: Adsorption of Pb, Cr and Ni Ions from Spent Lubrication Oil (SLO) Using Acid Modified Clay

Adsorption of Pb, Cr, and Ni ions from spent lubrication oil (SLO) by sulphuric acid modified clay (SAMC) was investigated considering the effect of contact time and temperature of the adsorption system. The removal percentage of the heavy metals was found to be temperature and contact time-dependent. Adsorption of the heavy metals increases with an increase in temperature and contact time with 95.0% - 100% adsorption recorded at the temperature of 331 K with the equilibration time of 12 hours. The thermodynamic and kinetics investigation of the adsorption process showed that the adsorption of these metals by the modified adsorbent is a spontaneous and endothermic physical adsorption process that followed the pseudo-second-order kinetic model.

Adsorption of Benzene in Batch System in Natural Clay and Sandy Soil

The adsorption potential of clay and sandy soil to remove benzene from liquid-phase system was examined. A series of batch adsorption tests were carried out for various concentrations of benzene (50 - 250 mg/l) in tightly corked 1000 ml flasks for clay and sandy soil, respectively. Equilibrium and kinetics data were obtained from the batch experiments. Adsorption increased with increasing initial benzene concentration. The equilibrium data obtained from the adsorption of benzene were well fitted to the Freundlich isotherm model. The adsorption kinetics process showed that the kinetic model of pseudo second-order was the best fit to the experimental data. The results showed that clay and sandy soil had good potential for the removal of aromatic hydrocarbon, benzene from aqueous solution.