Behavior and controlling factors of methane adsorption in Jurassic continental shale,northeastern Sichuan Basin

The behavior and controlling factors of natural gas adsorption in the Jurassic continental shale in the northeastern Sichuan Basin are studied based on the organic geochemical features,mineral compositions and pore structure parameters through a series of experiments on samples from the shale.Results show that the total gas content of the shale measured on-site is 0.1-5.3 cm^(3)/g,with an average of 0.7 cm^(3)/g.The methane isothermal adsorption curves show a trend of increasing first and then decreasing,indicating an obvious excessive adsorption.The shale has a maximum adsorption capacity(V^(L))of 0.44-3.59 cm^(3)/g,with an average of 1.64 cm^(3)/g,lower than that of marine shale in the same basin.The organic matter content and pore structure characteristics are identified as the two main factors controlling the adsorption capacity of the shale.Micropores in the shale are the main storage space for gas to be adsorbed.Due to well developed shell laminae and interlayers in the shale,calcite plays a more important role than clay minerals in affecting the adsorption of gas to the rock.The formation temperature and water content also significantly inhibit the gas adsorption to the shale.Compared with marine shale in the basin,the Jurassic continental shale is more heterogeneous and lower in TOC values.Furthermore,with a more widely developed clayey shale lithofacies and shell limy shale lithofacies as well as relatively less developed organic pores and micropores,the continental shale is inferior to marine shale in terms of gas adsorption capacity.

Bromate removal by activated carbon adsorption:material selection and impact factors study

Studies are conducted by using activated carbon process aimed at bromate removal from the raw water.Screening of activated carbon for bromate removal was performed in different activated carbons.GAC Merck possesses the highest iodine number and surface area,the highest number of basic groups and Vmeso,thereby contains the highest adsorption velocity and adsorption capacity.Impact factors of bromate removal on activated carbon were studied.Through static absorption experiments we studied the effect of adsorption time,pH,temperature,anions and organic matter on bromate removal.With the decrease of pH,removal of bromate enhanced,suggests that it may be possible to increase bromate reduction through pH control.The increase of temperature will be favorable to adsorption of bromate on activated carbon.Anions and organic matter can inhibit the adsorption of bromate on activated carbon through competing active sites.Bromate removal can be improved by controlling key water quality parameters.

Factors affecting phenol adsorption on clay-solidified grouting curtain

Batch experiments were conducted to study the adsorption of phenol on clay-solidified grouting curtain (CSGC) and the effects of contact time,pH and adsorbent concentration on the adsorption were investigated.Under the experimental conditions used,2 d was adequate to determine the equilibrium of phenol adsorption onto CSGC.The amount of phenol adsorbed by CSGC from an initial concentration of 100mg/L was found to be 8.4mg/g.The adsorption process includes particle diffusion and liquid film diffusion,and the latter is the predominating step of the adsorption process.The adsorption ability of CSGC decreased with pH but it increased non-linearly with the CSGC concentration.The optimized concentration for CSGC was found to be 20g/L for the adsorption of 100mg/L phenol.

Experimental and Numerical Research on Water Transport during Adsorption and Desorption in Cement-Based Materials

The durability of cement-based materials is related to water transport and storage in their pore network under different humidity conditions.To understand the mechanism and characteristics of water adsorption and desorption processes from the microscopic scale,this study introduces different points of view for the pore space model generation and numerical simulation of water transport by considering the“ink-bottle”effect.On the basis of the pore structure parameters(i.e.,pore size distribution and porosity)of cement paste and mortar with water-binder ratios of 0.3,0.4 and 0.5 obtained via mercury intrusion porosimetry,randomly formed 3D pore space models are generated using two-phase transformation on Gaussian random fields and verified via image analysis method of mathematical morphology.Considering the Kelvin-Laplace equation and the influence of“ink-bottle”pores,two numerical calculation scenarios based on mathematical morphology are proposed and applied to the generated model to simulate the adsorption-desorption process.The simulated adsorption and desorption curves are close to those of the experiment,verifying the effectiveness of the developed model and methods.The obtained results characterize water transport in cement-based materials during the variation of relative humidity and further explain the hysteresis effect due to“ink-bottle”pores from the microscopic scale.

Microthermokinetic study of xanthate adsorption on impurity-doped galena

Six kinds of galena with different impurities were synthesized and the effects of impurities on the floatability of galena were investigated. The thermodynamic and kinetic parameters on the galena surface were measured using microcalorimetry, and the adsorption configuration and energy of butyl xanthate on the surfaces of galena with different impurities were simulated by density functional theory. Flotation experiments showed that Ag and Bi significantly promoted the recovery of galena, while Zn, Sb, Mn, and Cu reduced the recovery of the flotation. Microthermokinetic results indicated that the absolute value of xanthate adsorption heat was directly proportional to the flotation recovery of galena. Adsorption heat and reaction rate coefficients of xanthate on galena containing Ag or Bi were larger than those on pure galena, but smaller on galena containing Cu or Sb. Additionally, the relationship between the heat of unsaturated adsorption of xanthate and the adsorption energy of impurity atom on galena surface was investigated.

Recent advances in chemical adsorption and catalytic conversion materials for Li–S batteries

Owing to their low cost,high energy densities,and superior performance compared with that of Li-ion batteries,Li–S batteries have been recognized as very promising next-generation batteries.However,the commercialization of Li–S batteries has been hindered by the insulation of sulfur,significant volume expansion,shuttling of dissolved lithium polysulfides(Li PSs),and more importantly,sluggish conversion of polysulfide intermediates.To overcome these problems,a state-of-the-art strategy is to use sulfur host materials that feature chemical adsorption and electrocatalytic capabilities for Li PS species.In this review,we comprehensively illustrate the latest progress on the rational design and controllable fabrication of materials with chemical adsorbing and binding capabilities for Li PSs and electrocatalytic activities that allow them to accelerate the conversion of Li PSs for Li–S batteries.Moreover,the current essential challenges encountered when designing these materials are summarized,and possible solutions are proposed.We hope that this review could provide some strategies and theoretical guidance for developing novel chemical anchoring and electrocatalytic materials for high-performance Li–S batteries.

Ion adsorption components in liquid/solid systems

Experiments on Zn^2＋ and Cd^2＋ adsorptions on vermiculite in aqueous solutions were conducted to investigate the widely observed adsorbent concentration effect on the traditionally defined adsorption isotherm in the adsorbate range 25--500 mg/L and adsorbent range 10--150 g/L. The results showed that the equilibrium ion adsorption density did not correspond to a unique equilibrium ion concentration in liquid phase. Three adsorbate/adsorbent ratios, the equilibrium adsorption density, the ratio of equilibrium adsorbate concentration in liquid phase to adsorbent concentration, and the ratio of initial adsorbate concentration to adsorbent concentration, were found to be related with unique values in the tested range. Based on the assumption that the equilibrium state of a liquid/solid adsorption system is determined by four mutually related components： adsorbate in liquid phase, adsorbate in solid phase, uncovered adsorption site and covered adsorption site, and that the equilibrium chemical potentials of these components should be equalized, a new model was presented for describing ion adsorption isotherm in liquid/solid systems. The proposed model fit well the experimental data obtained from the examined samples.

Adsorption and desorption behaviors of ssDNA molecules on mica surface by surface forces apparatus

An approach for studying the adsorption and desorption behaviors of single-stranded DNA（ ssDNA） molecules on the mica surface by the surface forces apparatus（ SFA） is reported,which can be used to characterize the precise thickness,configuration and mechanical properties of ssDNA layers on the mica surface at a certain buffer solution. The formation of ss DNA layers is first studied by tuning the ssDNA concentrations, and the experimental results indicate that the ss DNA concentration of 100 ng / μL is ideal for forming a ssDNA monolayer structure on the mica surface, and the hardwall value measured to be 1.04 nm under this circumstance is regarded as the thickness of the ssDNA monolayer confined on mica. The desorption behavior of ssDNA molecules from the mica surface is further studied by observing and comparing different shapes of the force-distance curves under certain conditions. It is found that the desorption of ss DNA molecules from the mica surface occurs as the monovalent salts are added into the gap buffer. It is inferred that the competition effect between monovalent and divalent salts can induce the release of ssDNA from substrate.The results also reveal that 10 mmol / L monovalent salts（ Na~＋）is sufficient for the desorption of ssDNA from mica. This work provides an applicable method to study the binding mechanism of ss DNA molecules on inorganic substrates.

Thermodynamic study of adsorption of phenolic compounds onto Amberlite XAD-4 polymeric adsorbents and its acetylized derivative MX-4

Adsorption equilibrium isotherms of phenolic compounds, phenol, p cresol, p chlorophenol and p nitrophenol, from aqueous solutions by Amberlite XAD 4 polymeric adsorbent and its acetylized derivative MX 4 within temperature range of 283 323K were obtained and fitted to the Freundlich isotherms. The capacities of equilibrium adsorption for all four phenolic compounds from their aqueous solutions increased around 20% on the acetylized resin, which may be contributed to the specific surface area and the partial polarity on the network. Estimations of the isosteric enthalpy, free energy, and entropy for the adsorption process were reported.

Pressure swing adsorption modeling of acetone and toluene on activated carbon

A five steps pressure swing adsorption process was designed for acetone and toluene mixtures separation and recovery. Dynamic distributions of gas phase content and temperature were investigated. Based on the theory of Soret and Dufour, a non-isothermal mathematical model was developed to simulate the PSA process. Effects of heat and mass transfer coefficients were studied. The coupled Soret and Dufour effects were also evaluated. It is found that the heat transfer coefficient has little effect on mass transfer in adsorption stage. However, it has some impacts in desorption stage. The maximum value of C/C0 increases by about 25% as heat transfer coefficient decreases. The temperature variation is less than 0.05 K with the change of mass transfer coefficient, so that the effect of mass transfer coefficient on heat transfer can be ignored. It is also concluded that the Soret and Dufour coupled effects are not obvious in pressure swing adsorption compared with fixed-bed adsorption.

Effects of the surface chemistry of macroreticular adsorbents on the adsorption of 1-naphthol/1-naphthylamine mixtures from water

The adsorption behaviors of 1-naphthol, 1-naphthylamine and l-naphthol/l-naphthylamine mixtures in water over two macroreticular adsorbents were investigated in single or binary batch systems at 293 K, 303 K and 313 K respectively. All the adsorption isotherms in the studied systems can be adequately fitted by Langmuir model. In the case of aminated macroreticular adsorbent NDA103, 1-naphthol is adsorbed to a larger extent than 1-naphthylamine; while, the opposite trend is found for nonpolar macroreticular adsorbent NDA100. It is noteworthy that at higher temperature（303 K and 313 K）, the total uptake amounts of 1-naphthol and 1-naphthylamine in all binary-component systems are obvious larger than the pure uptake amounts in single-component systems, which is presumably due to the cooperative effect primarily arisen from the hydrogen-bonding interaction between the loaded 1-naphthol and 1-naphthylamine molecules. The simultaneous adsorption systems were confirmed to be helpful to the selective adsorption towards 1-naphthol according to the larger selective index.

Particle concentration effect in adsorption/desorption of Zn(Ⅱ) on anatase type nano TiO_2

Adsorption/desorption in a new Zn（Ⅱ）-TiO2 adsorption system was investigated at different particle concentrations （Cp）. TEM, SEM and XRD analyses revealed that the TiO2 particles were an aggregation of nano-sized （approximately 10 nm） pure anatase-type TiO2. Adsorption experiments were carried out with particle concentrations of 100, 400 and 1000 mg/L, and their adsorption isotherms were found to decline successively, showing an obvious Cp effect. Desorption experiments indicated that adsorption in this system was irreversible, and the irreversibility increased with increasing Cp. These phenomena could be explained by the MEA （metastable equilibrium adsorption） theory and the Cp effect could be modeled well with an MEA-Freundlich-type Cp effect isotherm equation. This study may heln understand environmental behavior of contaminants on ultrafine natural particles.

Adsorption Mechanisms of Mesoporous Adsorbents in Solutions

Sieve effect, complexation, ionic exchange, electrostatic interaction, hydrogen bonding, hydrophobic interaction, and molecular recognition based on molecular imprinting are comprehensively discussed.

THERMODYNAMIC STUDY OF ADSORPTION OF PHENOLIC COMPOUNDS FROM AQUEOUS SOLUTION BY A WATER-COMPATIBLE HYPERCROSSLINKED POLYMERIC ADSORBENT

Equilibrium data for the adsorption of phenolic compounds, i.e., phenol, p-cresol, p-chlorophenol and p- nitrophenol from aqueous solutions by a water-compatible hypercrosslinked polymeric adsorbent (NJ-8) within temperature range of 283-323 K were obtained and correlated with a Freundlich-type of isotherm equation, so that equilibrium constants KF and n were obtained. The capacities of equilibrium adsorption for all the four phenolic compounds on the NJ-8 from aqueous solutions are around 2 times as high as those of Amberlite XAD-4, which may be attributed to the unusual micropore structure and the partial polarity on the network. The values of the enthalpy (always negative) are indicative of an exothermic process, which manifests the adsorption of all the four phenolic compounds on the two polymeric adsorbents to be a process of physical adsorption. The negative values of free energy change show that the solute is more concentrated on the adsorbent than in the bulk solution. The absolute free energy values of adsorption for NJ-8 are always higher than those for Amberlite XAD-4, which indicates that phenolic compounds are preferentially adsorbed on NJ-8. The negative values of the adsorption entropy are consistent with the restricted mobilities of adsorbed molecules of phenolic compounds as compared with the molecules in solution. The adsorption entropy values of phenolic compounds for NJ-8 are lower than those for Amberlite XAD-4, which means the micropores of NJ-8 require more orderly arranged adsorbate.

Synthesis and adsorption properties for Au(Ⅲ) of alkoxycarbonyl thiourea resin

A novel alkoxycarbonyl thiourea resin(ATR)was synthesized by monomer polymerization of oxydiethane-2,1-diyl dicarbonisothiocyanatidate and polyethylene polyamine,and characterized by FT-IR.The adsorption properties of ATR were investigated by batch test.The adsorption capacities for Au(Ⅲ),Ag(Ⅰ),Cu(Ⅱ),Zn(Ⅱ),Fe(Ⅲ),Ca(Ⅱ)and Mg(Ⅱ)are 4.65,4.40,0.40,0.90,0.86,0.0080 and 0.016 mmol/g,respectively,when the adsorption condition is as follows:contact time 24 h,temperature 30℃,initial concentration of Au(Ⅲ)5.08 mmol/L and that of other metals 0.10 mol/L,and concentration of acid 1.0 mol/L.The adsorption capacity for Au(Ⅲ)increases with the increase of contact time,temperature and initial concentration of Au(Ⅲ).The capacity after five adsorption-desorption cycles remains 90%that of the first time,and the separation factors of ATR for binary metal ion solutions are larger than 995,indicating that ATR is of good regeneration property and selectivity.XPS results show that the functional atoms of ATR supply electrons for Au and coordinate with Au during the adsorption.

Effect of an electrostatic field on gas adsorption and diffusion in tectonic coal

The characteristics of adsorption, desorption, and diffusion of gas in tectonic coal are important for the prediction of coal and gas outbursts. Three types of coal samples, of which both metamorphic grade and degree of damage is different, were selected from Tongchun, Qilin, and Pingdingshan mines. Using a series of experiments in an electrostatic field, we analyzed the characteristics of gas adsorption and diffusion in tectonic coal. We found that gas adsorption in coal conforms to the Langmuir equation in an electrostatic field. Both the depth of the adsorption potential well and the coal molecular electroneg- ativity increases under the action of an electrostatic field. A Joule heating effect was caused by changing the coal-gas system conductivity in an electrostatic field. The quantity of gas adsorbed and AP result from competition between the depth of the adsorption potential well, the coal molecular electronegativ- ity, and the Joule heating effect. △P peaks when the three factors control behavior equally. Compared with anthracite, the impact of the electrostatic field on the gas diffusion capacity of middle and high rank coals is greater. Compared with the original coal, the gas adsorption quantity,△P, and the gas diffusion capacity of tectonic coal are greater in an electrostatic field. In addition, the smaller the particle size of tectonic coal, the larger the△P.

Binding and Adsorption Energies of Heavy Metal Ions with Hapli-Udic Argosol and Ferri-Udic Argosol Particles

Gibbs free binding energy and adsorption energy between cations and charged soil particles were used to evaluate the interactions between ions and soil particles. The distribution of Gibbs free adsorption energies could not be determined experimentally before the development of Wien effect measurements in dilute soil suspensions. In the current study, energy relationships between heavy metal ions and particles of Hapli-Udic Argosol （Alfisol） and Ferri-Udic Argosol were inferred from Wien effect measurements in dilute suspensions of homoionic soil particles （〈 2 μm） of the two soils, which were saturated with ions of five heavy metals, in deionized water. The mean Gibbs free binding energies of the heavy metal ions with Hapli-Udic Argosol and Ferri-Udic Argosol particles diminished in the order of Pb^2＋ 〉 Cd^2＋ 〉 Cu^2＋ 〉 Zn^2＋ 〉 Cr^3＋, where the range of binding energies for Hapli-Udic Argosol （7.25-9.32 kJ mol^-1） was similar to that for Ferri-Udic Argosol （7.43-9.35 kJ mol^-1）. The electrical field-dependent mean Gibbs free adsorption energies of these heavy metal ions for Hapli-Udic Argosol and for Ferri-Udic Argosol descended in the order： Cu^2＋ 〉 Cd2^＋ 〉 Pb^2＋ 〉 Zn^2＋ 〉 Cr^3＋, and Cd^2＋ 〉 Cu^2＋ 〉 Pb^2＋ 〉 Zn^2＋ 〉 Cr^3＋, respectively. The mean Gibbs free adsorption energies of Cu^2＋, Zn^2＋, Cd^2＋, Pb^2＋, and Cr^3＋ at a field strength of 200 kV cm^-1, for example, were in the range of 0.8-3.2 kJ mo1^-1 for the two soils.

Recent Advances on Porous Materials for Synergetic Adsorption and Photocatalysis

Porous photocatalysts are promising materials capable of simultaneously adsorbing and oxidizing/reducing target species,showing great potentials in environmental remediation and energy generation.This review offered a comprehensive overview of the recent progress in design,fabrication,and applications of porous photocatalysts,including carbon-based semiconductors,metal oxides/sulfides,metal–organic frameworks,and adsorbent–photocatalyst hybrids.The fundamental understanding of the structure–performance relationships of porous materials together with the in-depth insights into the synergetic effects between adsorption and photocatalysis was presented.The strategies to further improve the photocatalytic activity of porous photocatalysts were proposed.This review would provide references and outlooks of constructing efficient porous materials for adsorptive and photocatalytic removal of pollutants and energy production.

Adsorption of Dissolved Organic Matter by Ferrallitic Soils

Batch experiments and XAD resin were used to investigate the adsorption of dissolved organic matter(DOM) by ferrallitic soils. The effects of soil properties and DOM characteristics on the adsorption were also studied to reveal the adsorption mechanism. The results showed that:(1) ferrallitic soils were high in DOM adsorption capacity,which increased with initial DOM concentrations,and the kinetics of DOM adsorption in the ferrallitic soils can be divided into the two stages: fast and slow reactions,it could be better fitted by first-order model;(2) the adsorption isotherms of DOM on ferrallitic soils could be better fitted by Freundlich equation,indicating the adsorption process was a physical multilayer adsorption process;( 3) for different soils,the adsorption capacity of DOM was listed as follows: rhodic ferralsol > haplic ferralsol > paddy soil,for example,adsorbing capacity of compost DOM was up to 594. 906,309. 317 and 206. 316 mg / kg in the initial concentration of 50 mg / L,positively correlated with CEC,free iron oxide,free aluminium oxide and clay content,while negatively correlated with sand content;(4) for different DOMs,higher hydrophobic DOM had the larger adsorption capacity,which listed as follows: compost DOM( H-DOM) > soil DOM( M-DOM) > straw DOM( L-DOM);(5) for different DOM components,the adsorption capacity decreased as follows: hydrophobic neutrals( HON) > acid-insoluble matter( AIM) > hydrophobic bases( HOB) > hydrophobic acids( HOA) > hydrophillic matter( HIM),and the chain structure of aliphatic alkanes and higher aromaticity in DOM were the key factors influencing adsorption capacity as revealed by fourier-transform infrared spectroscopy( FT-IR);(6)the contribution to DOM adsorption by different fractions was the result of their adsorption capacities and contents. For different hydrophobic DOM,hydrophobic matter's contribution( HO) was more than HIM,up to 69. 43%85. 08%. For different polar fractions,H-DOM: HOA( 40. 24%) > HON( 39.10%) > HIM( 14.92%) > AIM( 3.82%) > HOB( 1.88%); L-DOM: HOA( 33. 50%) > HIM( 30. 57%) > HON( 24. 81%) > AIM( 7. 45%) > HOB( 3.68%);( 7) The presence of native DOM in soil impeded the exotic DOM adsorption by soil,especially for high hydrophobic DOM.

Enhancement of catalytic activity by homo-dispersing S_2O_8^(2–)-Fe_2O_3 nanoparticles on SBA-15 through ultrasonic adsorption

Mesoporous superacids S2O82–-Fe2O3/SBA-15(SFS)with active nanoparticles are prepared by ultrasonic adsorption method.This method is adopted to ensure a homo-dispersed nanoparticle active phase,large specific surface area and many acidic sites.Compared with bulk S2O82–-Fe2O3,Br?nsted acid catalysts and other reported catalysts,SFS with an Fe2O3 loading of 30%(SFS-30)exhibits an outstanding activity in the probe reaction of alcoholysis of styrene oxide by methanol with 100%yield.Moreover,SFS-30 also shows a more excellent catalytic performance than bulk S2O82–-Fe2O3 towards the alcoholysis of other ROHs(R=C2H5-C4H9).Lewis and Bronsted acid sites on the SFS-30 surfaces are confirmed by pyridine adsorbed infrared spectra.The highly efficient catalytic activity of SFS-30 may be attributed to the synergistic effect from the nano-effect of S2O82–-Fe2O3 nanoparticles and the mesostructure of SBA-15.Finally,SFS-30 shows a good catalytic reusability,providing an 84.1%yield after seven catalytic cycles.