Flotation is the most common method to recover valuable minerals by selective adsorption of collectors on target mineral surfaces.However,in subsequent hydrometallurgy of mineral flotation concentrates,the adsorbed co...Flotation is the most common method to recover valuable minerals by selective adsorption of collectors on target mineral surfaces.However,in subsequent hydrometallurgy of mineral flotation concentrates,the adsorbed collectors must be desorbed since it can adversely affect the efficiency of metallurgical process and produce wastewater.ZL,as a fatty acid mixture,is a typical industrially used collector for scheelite flotation in China.Sodium oleate(NaOL)has similar fatty acid group as ZL.In this study,the desorption behavior of NaOL/ZL from scheelite surface by a physical method of stirring at a low temperature was investigated.NaOL desorption tests of single mineral showed that a desorption rate of 77.75% for NaOL from scheelite surface into pulp was achieved in a stirring speed of2500 r/min at 5℃in a neutral environment.Under the above desorption condition,in the pulp containing desorbed collector by adding extra 30% normal NaOL dosage,the scheelite recovery reached about 95% in the single mineral flotation test.Desorption and reuse of ZL collector for the flotation of real scheelite ore showed only a 75%normal dosage of ZL could produce a qualified rough concentrate.The atomic force microscope(AFM)tests showed that after desorption treatment of low temperature and strong stirring,the dense strip-like structure of NaOL on the scheelite surface was destroyed to be speck-like.Molecular dynamics simulations(MDS)demonstrated that the adsorption energy between NaOL and scheelite surface was more negative at 25℃(-13.39 kcal/mol)than at 5℃(-11.50 kcal/mol)in a neutral pH,indicating that a low temperature was beneficial for the desorption of collector from mineral surface.Due to its simplicity and economy,the method we proposed of desorption of collector from mineral surface and its reuse for flotation has a great potential for industrial application.展开更多
Microplastics loaded with phenanthrene and derivatives are widely detected in aquatic environments,and the coating of natural minerals or organic macromolecules may change the environmental behavior of microplastics.I...Microplastics loaded with phenanthrene and derivatives are widely detected in aquatic environments,and the coating of natural minerals or organic macromolecules may change the environmental behavior of microplastics.In this study,three kinds of composites with different coverage were prepared by coating goethite on the surface of polyvinyl chloride microplastics to investigate the adsorption and desorption behavior of phenanthrene(PHE)and 1-hydroxyphenanthrene(1-OHPHE),and the effect of mucin on desorption was inves-tigated.The results showed that goethite promoted the adsorption of PHE and 1-OHPHE by increasing the specific surface area of the composites.With the increase of the cover de-gree,the adsorption of PHE decreased because of the decrease in hydrophobicity;while the adsorption of 1-OHPHE initially increased and then decreased with the contributions of hydrophobic interaction and hydrogen bond.The adsorption of 1-OHPHE could be influenced by the pH and ionic strength primarily through electrostatic interactions and Ca2+bridg-ing.The goethite significantly increased the desorption hysteresis for two chemicals due to the complicated pore structures and increased adsorption affinity.Mucin promoted the desorption of PHE through competitive adsorption,and inhibit the desorption of 1-OHPHE through hydrophobic interaction,hydrogen bonding and Ca2+bridging.This study elucidated the effects of natural minerals on the adsorption and desorption behavior of organic pollutants on microplastics,briefly discussed the effects of organic macromolecules on the desorption behavior of pollutants with different properties,and emphasized the different environmental behaviors of pollutants.展开更多
This paper summarizes the mechanisms and environmental effects of interactions between microplastics and surfactants: surfactants adsorb onto microplastics surfaces through hydrophobic interactions and electrostatic f...This paper summarizes the mechanisms and environmental effects of interactions between microplastics and surfactants: surfactants adsorb onto microplastics surfaces through hydrophobic interactions and electrostatic forces, changing their surface properties and transport behavior. In addition, microplastics act as carriers influencing surfactant distribution. Environmental factors (pH, ionic strength, etc. ) significantly regulate this process. Current research still has limitations in areas such as desorption kinetics and combined pollution effects, necessitating in-depth studies under environmentally relevant conditions to provide a basis for risk assessment.展开更多
Understanding how different vegetation-based restoration practices alter soil chemical and microbial characteristics is crucial,as restoration practices influence phosphorus(P)transformation and fractions and modify P...Understanding how different vegetation-based restoration practices alter soil chemical and microbial characteristics is crucial,as restoration practices influence phosphorus(P)transformation and fractions and modify P adsorption behavior during the restoration process of degraded land.This study investigated the impacts of vegetation-based restoration practices on soil chemical and microbial parameters,P fractions,and patterns of P adsorption and desorption,and highlighted the combined influence on P availability.To evaluate the impact of vegetation-based restoration practices on P fractions and adsorption behavior in the semi-arid degraded land in India,this study compared three distinct tree-based restoration systems,including Leucaena leucocephala(Lam.)de Wit-based silviculture system(SCS),Acacia nilotica(L.)Willd.ex Delile-based silvopasture system(SPS),and Emblica officinalis Gaertn-based hortipasture system(HPS),with a natural grassland system(NGS)and a degraded fallow system(FS)as control.The soil samples across various soil depths(0-15,15-30,and 30-45 cm)were collected.The findings demonstrated that SCS,SPS,and HPS significantly improved soil organic carbon(SOC)and nutrient availability.Moreover,SCS and SPS resulted in increased microbial biomass phosphorus(MBP)content and phosphatase enzyme activity.The P fractionation analysis revealed that ferrum-associated phosphorus(Fe-P)was the major P fraction,followed by aluminum-associated phosphorus(Al-P),reflecting the dominance of ferrum(Fe)and aluminum(Al)oxides in the semi-arid degraded land.Compared with FS,vegetation-based restoration practices significantly increased various P fractions across soil depths.Additionally,P adsorption and desorption analysis indicated a lower adsorption capacity in tree-based restoration systems than in FS,with FS soils adsorbing higher P quantities in the adsorption phase but releasing less P during the desorption phase.This study revealed that degraded soils responded positively to ecological restoration in terms of P fraction and desorption behavior,influencing the resupply of P in restoration systems.Consequently,litter rich N-fixing tree-based restoration systems(i.e.,SCS and SPS)increased total phosphorus(TP)stock for plants and sustained the potential for long-term P supply in semi-arid ecosystems.With the widespread adoption of restoration practices across degraded landscapes,SCS and SPS would significantly contribute to soil restoration and improve productivity by maintaining the soil P supply in semi-arid ecosystems in India.展开更多
[Objective]The research aimed to provide scientific reference for reasonable utilization of polyacrylamide(PAM).[Method]After PAM treatment,the soil aggregates were classified through dry sieve analysis and the adsorp...[Objective]The research aimed to provide scientific reference for reasonable utilization of polyacrylamide(PAM).[Method]After PAM treatment,the soil aggregates were classified through dry sieve analysis and the adsorption capacity and desorption capacity of all soil aggregates to phosphorus at different phosphorus concentrations were analyzed.[Result] The phosphorus adsorption and desorption of soil sample treated by PAM declined. The amount of phosphorus adsorption increased with the increase of phosphorus concentration and this increase was fast in low phosphorus concentration area but slow in high phosphorus concentration area.At different phosphorus concentrations,adsorption showed a へ shape changing trend.The phosphorus adsorption was related to phosphorus concentration and the 2-3 mm aggregate had the highest desorption rate while 0.1-0.25 mm aggregate and 0.45-1 mm aggregate had lowest desorption rate.[Conclusion]The PAM treatment generated significant influence on phosphorus adsorption and analytic features of aggregate in all size fractions.展开更多
The Cr（III） desorption experiments of Gaomiaozi （GMZ） bentonite in aqueous solutions were performed. The variables affecting the desorption behaviors, such as contact time, concentration of the desorbent, pH value...The Cr（III） desorption experiments of Gaomiaozi （GMZ） bentonite in aqueous solutions were performed. The variables affecting the desorption behaviors, such as contact time, concentration of the desorbent, pH value of the solution, temperature and desorption isotherms, were investigated by the batch experiments. The results show that the adsorbed Cr（III） on GMZ bentonite can be easily extracted by the desorbent. Kinetics examination shows that desorption is slower than adsorption, and the desorption rate increases with time and reaches the equilibrium after 3 h. The final desorption ratios of Cr（III） are 89.4%, 56.5%and 77.2%in the desorption solution with 0.1 mol/L HCl, 1 mol/L NaCl, and 1 mol/L CaCl2, respectively, and the concentration can promote the desorption progress. Furthermore, the results of successive regeneration cycles indicate that the bentonite has a good regeneration ability and reusability. The pH value is an important factor in the Cr（III） desorption from the GMZ bentonite. The results of adsorption and desorption isotherms show that both adsorption and desorption isotherms are consistent with the Freundlich equation. The comparison of adsorption and desorption isotherms implies that the adsorption/desorption hysteresis is negligible and the transport of Cr（III） in bentonite can be described by a reversible adsorption process.展开更多
The adsorption and desorption of isoliquiritigenin and liquiritigenin to different types of carbon nanotubes （CNTs） were comparatively studied in this study. The pore structure, specific surface area, surface morpho...The adsorption and desorption of isoliquiritigenin and liquiritigenin to different types of carbon nanotubes （CNTs） were comparatively studied in this study. The pore structure, specific surface area, surface morphologies and functional groups of the CNTs were tested by N2 adsorption, scanning electron microscope （SEM） and infrared spectra （IR）. The investigation of dynamic adsorption, isothermal equilibrium adsorption and desorption of isoliquiritigenin and liquiritigenin to CNTs demonstrated that the adsorption amount on oxidized multi-walled carbon nanotubes （o-MWCNTs） was greater than that on raw multi-walled carbon nanotubes （r-MWCNTs）, especially the adsorption of isoliquiritigenin to o-MWCNTs. The data of equilibrium adsorption were better represented by the Freundlich isotherm model. In addition, the adsorbed amount per unit CNTs was decreased when the temperature got higher. From the results of isothermal equilibrium adsorption and desorption to CNTs, it could be inferred that o-MWCNTs had higher adsorption to isoliquiritigenin and liquiritigenin than r-MWCNTs. Additionally, o-MWCNTs had a better desorption efficiency to isoliquiritigenin and liquiritigenin （about 48.57% and 32.86%） than r-MWCNTs （about 24.56% and 17.46%）.展开更多
[Objective] This study aimed to investigate the adsorption and desorption characteristics of cadmium and lead in typical paddy soils of Jiangxi Province. [Method] Gleyed paddy soil and waterloggogenic paddy soil were ...[Objective] This study aimed to investigate the adsorption and desorption characteristics of cadmium and lead in typical paddy soils of Jiangxi Province. [Method] Gleyed paddy soil and waterloggogenic paddy soil were collected from Jiangxi Province and used as experimental materials to investigate single and com- petitive adsorption and desorption behaviors of cadmium and lead by batch equilib- rium method. The environmental risk of the presence of cadmium and lead in paddy soils was assessed using distribution coefficients. [Result] Under equal ratio condi- tions, the adsorption capacity of lead by two types of paddy soils was higher than that of cadmium, and the adsorption rate in waterloggogenic paddy soil was higher than that in gleyed paddy soil. The desorption capacity of cadmium by two types of paddy soils was higher than that of lead, and the desorption rate in gleyed paddy soil was higher than that in waterloggogenic paddy soil. Under competitive condi- tions, the adsorption capacity of cadmium and lead by paddy soils was significantly reduced compared with single ion system, while the desorption rate was remarkably improved. The potential environmental risk of cadmium contamination was greater than that of lead in paddy soils. Moreover, environmental risks of cadmium and lead were reduced with the increase of pH, which increased significantly under the coex- istence state. [Conclusion] In the coexistence of cadmium and lead, cadmium con- tamination should be controlled and avoided compared with lead contamination in paddy soils.展开更多
The adsorption and desorption kinetic of natural zeolite on NH4＋ was stud-ied by lab analysis. The results showed that the adsorption and desorption kinetic of natural zeolite on NH4＋ coincided with the first-order ...The adsorption and desorption kinetic of natural zeolite on NH4＋ was stud-ied by lab analysis. The results showed that the adsorption and desorption kinetic of natural zeolite on NH4＋ coincided with the first-order kinetics, modified Freundlich equation, parabolic diffusion model, and heterogeneous diffusion model. The desorp-tion of the adsorbed NH4＋ was far rapider than the adsorption, which can be fin-ished within 60 min.展开更多
This work was undertaken to investigate the behaviors and kinetics of toluene adsorption and desorption on activated carbons with varying pore structure. Five kinds of activated carbon from different raw materials wer...This work was undertaken to investigate the behaviors and kinetics of toluene adsorption and desorption on activated carbons with varying pore structure. Five kinds of activated carbon from different raw materials were selected. Adsorption isotherms and breakthrough curves for toluene were measured. Langmuir and Freundlich equations were fitted to the equilibrium data, and the Freundlich equation was more suitable for simulating toluene adsorption. The process consisted of monolayer, multilayer and partial active site adsorption types. The effect of the pore structure of the activated carbons on toluene adsorption capacity was investigated. The quasi-first-order model was more suitable for describing the process than the quasi-second-order model. The adsorption data was also modeled by the internal particle diffusion model and it was found that the adsorption process could be divided into three stages. In the external surface adsorption process, the rate depended on the specific surface area. During the particle diffusion stage, pore structure and volume were the main factors affecting adsorption rate. In the final equilibrium stage, the rate was determined by the ratio of meso-and macro-pores to total pore volume. The rate over the whole adsorption process was dominated by the toluene concentration. The desorption behavior of toluene on activated carbons was investigated,and the process was divided into heat and mass transfer parts corresponding to emission and diffusion mechanisms, respectively. Physical adsorption played the main role during the adsorption process.展开更多
Fourier-transform infrared（FT-IR） spectroscopic experiments were carried out during phosphate adsorption on highly crystalline gibbsite, poorly crystalline 2-line-ferrihydrite and amorphous iron–aluminum–hydroxide...Fourier-transform infrared（FT-IR） spectroscopic experiments were carried out during phosphate adsorption on highly crystalline gibbsite, poorly crystalline 2-line-ferrihydrite and amorphous iron–aluminum–hydroxide mixtures in the molar ratio 1：0, 10：1, 5：1, 1：1, 1：5, 1：10 and 0：1. The OH stretching vibrational bands were utilized to analyze changes in structural and surface OH groups during adsorption, because the position of characteristic P／O vibrational bands can shift depending on reaction conditions, pH or adsorbed phosphate content.Adsorption and desorption kinetics were studied at pH6 and different initial phosphate concentrations to achieve varying phosphate coverage on the mineral surfaces. For gibbsite the formation of AlHPO4 and Al2HPO4 can be assumed, while for ferrihydrite, a FeHPO4 or Fe2PO4 complex and the precipitation of FePO4 with longer equilibration time were proposed.Fe2HPO4 or a Fe2PO4 surface complex was deduced for Fe-hydroxides, an AlH2PO4 surface complex was identified for Al-hydroxide, and both displayed either hydrogen bonds to neighboring hydroxyl groups or hydrogen bonds to outer-sphere complexes. Fe：Al-hydroxide mixtures with high Al ratios showed a low phosphate desorption rate, while ferrihydrite and the Fe：Al-hydroxide mixtures with high Fe ratios had almost negligible desorption rates. It was concluded that within the weakly associated amorphous FeO（OH） materials, FePO4 precipitated, which was bound by outer-sphere hydrogen bonds. With high Al ratios, desorption increased, which indicated weaker phosphate binding of both inner-sphere and outer-sphere complexes and hence, either no or minor quantities of precipitate. Ferrihydrite showed a more rigid structure and a lower extent of precipitation compared to amorphous Fe-hydroxide.展开更多
A novel amphoteric granular lignin adsorbent(AGLA) was prepared using magnesium lignosulfonate as a raw material which was provided by a straw sulfite pulp mill in Guangdong Province, China. A reactive dye(red K-3B) w...A novel amphoteric granular lignin adsorbent(AGLA) was prepared using magnesium lignosulfonate as a raw material which was provided by a straw sulfite pulp mill in Guangdong Province, China. A reactive dye(red K-3B) was used as an adsorbate to investigate the adsorption behavior by static and mobile ways. The removal of reactive red K-3B was found to be initially pH and concentration dependent. Moreover, an increase of solution temperature ranging from 5℃ to 60℃ helped to enhance the rate of intraparticle diffusion of adsorbate and changes in the size of the pores of the adsorbent and thus to reduce the adsorption time. The total breakthrough adsorption capacity was 531 mg/g, and the saturated adsorption capacity was 560 mg/g, which prevailed over the activated carbons evidently. The reactive red K-3B adsorbed on AGLA could be recovered with a mixture of alcohol, NaCl and HCl aqueous solutions. The recovery percentage could reach 92.4%.展开更多
Effects of dissolved organic matter (DOM) on adsorption and desorption of Hg were investigated in two kinds of soils, Xanthi-Udic Ferralosols (XUF) and Typic Purpli-Udic Cambosols (TPUC). The DOM was obtained from hum...Effects of dissolved organic matter (DOM) on adsorption and desorption of Hg were investigated in two kinds of soils, Xanthi-Udic Ferralosols (XUF) and Typic Purpli-Udic Cambosols (TPUC). The DOM was obtained from humus soil (DOMH), rice straw (DOMR), and pig manure (DOMP). The presence of DOM obviously reduced Hg maximum adsorption capacity with up to 40% decreases over the control, being an order of DOMH (250.00 mg/kg)< DOMR (303.03 mg/kg) < DOMP (322.58 mg/kg) < CK (control 416.67 mg/kg) for the...展开更多
Four different types of adsorbents, SBA-15, MCM-41, NaY and SiO2, were used to study the dynamic adsorption/desorption of toluene. To further investigate the influence of pore structure on its adsorption performance, ...Four different types of adsorbents, SBA-15, MCM-41, NaY and SiO2, were used to study the dynamic adsorption/desorption of toluene. To further investigate the influence of pore structure on its adsorption performance, two SBA-15 samples with different microspores were also selected. It is shown that microporous material NaY has the largest adsorption capacity of 0.2873 mL/g, and the amorphous SiO2 exhibits the least capacity of 0.1003 mL/g. MCM-41 also shows a lower break through capacity in spite of the relatively small pore diameter, because it can not provide the necessary small geometric confinement for the tiny adsorbates. However, the mesoporous SBA-15 silica with certain micropore volume shows relatively higher adsorption capacity than that of MCM-41 silica. The presence of micropores directly leads to an increase in the dynamic adsorption capacity of toluene. Although NaY has the highest adsorption capacity for toluene, its complete desorption temperature for toluene is high （〉 350°C）, which limits its wide application. On the contrary, mesoporous silica materials exhibits a good desorption performance for volatile organic compounds at lower temperatures. Among these materials mesoporous SBA-15 samples, with a larger amount micropores and a lower desorption temperature, are a potentially interesting adsorbent for the removal of volatile organic compounds. This behavior should been related with the best synergetic effect of mesopores and micropores.展开更多
The adsorption and desorption of Cu（Ⅱ） and Pb（Ⅱ） on upland red soil,and paddy soils which were originated from the upland soil and cultivated for 8,15,35 and 85 years,were investigated using the batch method.The...The adsorption and desorption of Cu（Ⅱ） and Pb（Ⅱ） on upland red soil,and paddy soils which were originated from the upland soil and cultivated for 8,15,35 and 85 years,were investigated using the batch method.The study showed that the organic matter content and cation exchange capacity （CEC） of the soils are important factors controlling the adsorption and desorption of Cu（Ⅱ） and Pb（Ⅱ）.The 15-Year paddy soil had the highest adsorption capacity for Pb（Ⅱ）,followed by the 35-Year paddy soil.Both the 35-Year paddy soil and 15-Year paddy soil adsorbed more Cu（Ⅱ） than the upland soil and other paddy soils.The 15-Year paddy soils exhibited the highest desorption percentage for both Cu（Ⅱ） and Pb（Ⅱ）.These results are consistent with the trend for the CEC of the soils tested.The high soil CEC contributes not only to the adsorption of Cu（Ⅱ） and Pb（Ⅱ） but also to the electrostatic adsorption of the two heavy metals by the soils.Lower desorption percentages for Cu（Ⅱ） （36.7% to 42.2%） and Pb（Ⅱ） （50.4% to 57.9%） were observed for the 85-Year paddy soil.The highest content of organic matter in the soil was responsible for the low desorption percentages for the two metals because the formation of the complexes between the organic matter and the metals could increase the stability of the heavy metals in the soils.展开更多
Monosulfuron-ester is a new,low rate,sulfonylurea herbicide that is being promoted for annual broadleaf and gramineal weed control;however,there is a lack of published information on its behavior in soils.The adsorpti...Monosulfuron-ester is a new,low rate,sulfonylurea herbicide that is being promoted for annual broadleaf and gramineal weed control;however,there is a lack of published information on its behavior in soils.The adsorption and desorption of monosulfuronester by seven type soils were measured using a batch equilibrium technique.The results showed that the Freundlich equation fitted its adsorption and desorption well,and the Freundlich constant values （K f-ads ） ranged from 0.88 to 5.66.Adsorption isotherms were nonlinear with 1/n f-ads values 1.Soil pH,organic matter （OM）,and clay content were the main factors influencing its adsorption and desorption.Adsorption and desorption were negatively correlated with pH 4.0–8.0 while positively correlated with OM and clay content.The adsorption of monosulfuron-ester was mainly a physical process,because its free energy （？G） in seven soils was less than 40 kJ/mol.Monosulfuron-ester adsorption by three soils increased with increasing CaCl 2 concentration using CaCl 2 as a background electrolyte.Monosulfuron-ester desorption was hysteretic in all tested soils.展开更多
The behavior of herbicide acetochlor adsorption desorption to soil in the presence of humic acid (HA), anionic surfactant sodium dodecylbenzene sulfonate (SDBS), cationic surfactant hexadecyltrimethyl ammonium bromi...The behavior of herbicide acetochlor adsorption desorption to soil in the presence of humic acid (HA), anionic surfactant sodium dodecylbenzene sulfonate (SDBS), cationic surfactant hexadecyltrimethyl ammonium bromide (HDAB) and NH 4NO 3 as a chemical fertilizer was studied. Observed acetochlor adsorption isotherm were well described using Freundlich isotherm equation, from which the desorption isotherm equation has been deduced. The deduced equation can more directly describe acetochlor desorption process. The results showed that the enhance of acetochlor adsorption capacity by solid HA was greater than by soluble HA. The presence of NH 4NO 3 can slightly enhance acetochlor adsorption to soil by comparison with that measured in NH 4NO 3 free solution. In soil water system, surfactant acetochlor interaction is very complex, and the surfactant adsorptions as well as acetochlor adsorption need to be considered. When acetochlor soil suspensions contained lower concentration SDBS or HDAB (40 mg/L), K f for acetochlor adsorption was decreased in comparison to that measured in SDBS or HDAB free solution. When acetochlor soil suspensions contained higher concentration SDBS or HDAB (corresponding 1400 mg/L or 200 mg/L), K f for acetochlor adsorption was increased in comparison to that measured in SDBS or HDAB free solution.展开更多
Effects of particle size on CH4 and CO2adsorption and desorption characteristics of coals are investigated at 308 K and pressures up to 5.0 MPa.The gas adsorption and desorption isotherms of coals with particle sizes ...Effects of particle size on CH4 and CO2adsorption and desorption characteristics of coals are investigated at 308 K and pressures up to 5.0 MPa.The gas adsorption and desorption isotherms of coals with particle sizes ranging from 250 μm to 840 μm are measured via the volumetric method,and the Langmuir model is used to analyse the experimental results.Coal particle size is found to have an obvious effect on the coal pore structure.With the decrease of coal particle size in the process of grinding,the pore accessibility of the coal,including the specific surface area and pore volume,increases.Hence,coal with smaller particle size has higher specific surface area and higher pore volume.The ability of adsorption was highly related to the pore structure of coal,and coal particle size has a significant influence on coal adsorption/desorption characteristics,including adsorption capacity and desorption hysteresis for CH4 and CO2,i.e.,coal with a smaller particle size achieves higher adsorption capacity,while the sample with a larger particle size has lower adsorption capacity.Further,coal with larger particle size is also found to have relatively large desorption hysteresis.In addition,dynamic adsorption performances of the samples are carried out at 298 K and at pressures of 0.1 MPa and 0.5 MPa,respectively,and the results indicate that with the increase of particle size,the difference between CO2 and CH4adsorption capacities of the samples decreases.展开更多
Diphenylarsinic acid （DPAA） is formed during the leakage of aromatic arsenic chemical weapons in soils, is persistent in nature, and results in arsenic contamination in the field. The adsorption and desorption chara...Diphenylarsinic acid （DPAA） is formed during the leakage of aromatic arsenic chemical weapons in soils, is persistent in nature, and results in arsenic contamination in the field. The adsorption and desorption characteristics of DPAA were investigated in two typical Chinese soils, an Acrisol （a variable-charge soil） and a Phaeozem （a constant-charge soil）. Their thermodynamics and some of the factors influencing them （i.e., initial pH value, ionic strength and phosphate） were also evaluated using the batch method in order to understand the environmental fate of DPAA in soils. The results indicate that Acrisol had a stronger adsorption capacity for DPAA than Phaeozem. Soil DPAA adsorption was a spontaneous and endothermic process and the amount of DPAA adsorbed was affected significantly by variation in soil pH and phosphate. In contrast, soil organic matter and ionic strength had no significant effect on adsorption. This suggests that DPAA adsorption may be due to specific adsorption on soil mineral surfaces. Therefore, monitoring the fate of DPAA in soils is recommended in areas contaminated by leakage from chemical weapons.展开更多
In many sources of volatile organic compounds (VOCs), large amounts of water vapor come from the air and the reactors. The relative humidity (RH) of exhaust gas is normally >60% and is supersaturated. Maintaining t...In many sources of volatile organic compounds (VOCs), large amounts of water vapor come from the air and the reactors. The relative humidity (RH) of exhaust gas is normally >60% and is supersaturated. Maintaining the property of adsorbent on VOCs in a highly humid gas stream is a serious industrial problem. In this study, the adsorption/desorption behavior of toluene in a micro-mesoporous polymeric resin was investigated in a highly humid environment to explore the influence of abound water vapor on resin adsorption and regeneration. This resin could selectively adsorb toluene at an RH of 80%, and its adsorption property was unaffected by the presence of water vapor. In the case of humidity saturation, the resin displayed a high adsorption capacity at a moisture content of <30%. Therefore, the polymer resin is an excellent water-resistant adsorbent of VOCs. In the regenerative experiment, the resin maintained its original adsorption capability after four adsorption/ desorption cycles of toluene purging with nitrogen gas at 120℃. The resin exhibited excellent regeneration performance at high humidity.展开更多
基金financially supported by the National Natural Science Foundation of China(Nos.52304314 and U23A20602)the Open Fund of the Key Laboratory of Mineral Metallurgical Resources Utilization and Pollution Control,Ministry of Ecology and Environment+3 种基金China(No.HB202406)the Fundamental Research Funds for the Central Universities of Central South University,China(Nos.CX20240021 and 2024ZZTS0008)the Innovation and Entrepreneurship Funding Project for College Students of Central South UniversityChina(No.S202410533166)。
文摘Flotation is the most common method to recover valuable minerals by selective adsorption of collectors on target mineral surfaces.However,in subsequent hydrometallurgy of mineral flotation concentrates,the adsorbed collectors must be desorbed since it can adversely affect the efficiency of metallurgical process and produce wastewater.ZL,as a fatty acid mixture,is a typical industrially used collector for scheelite flotation in China.Sodium oleate(NaOL)has similar fatty acid group as ZL.In this study,the desorption behavior of NaOL/ZL from scheelite surface by a physical method of stirring at a low temperature was investigated.NaOL desorption tests of single mineral showed that a desorption rate of 77.75% for NaOL from scheelite surface into pulp was achieved in a stirring speed of2500 r/min at 5℃in a neutral environment.Under the above desorption condition,in the pulp containing desorbed collector by adding extra 30% normal NaOL dosage,the scheelite recovery reached about 95% in the single mineral flotation test.Desorption and reuse of ZL collector for the flotation of real scheelite ore showed only a 75%normal dosage of ZL could produce a qualified rough concentrate.The atomic force microscope(AFM)tests showed that after desorption treatment of low temperature and strong stirring,the dense strip-like structure of NaOL on the scheelite surface was destroyed to be speck-like.Molecular dynamics simulations(MDS)demonstrated that the adsorption energy between NaOL and scheelite surface was more negative at 25℃(-13.39 kcal/mol)than at 5℃(-11.50 kcal/mol)in a neutral pH,indicating that a low temperature was beneficial for the desorption of collector from mineral surface.Due to its simplicity and economy,the method we proposed of desorption of collector from mineral surface and its reuse for flotation has a great potential for industrial application.
基金supported by the National Natural Science Foundation of China(Nos.42077337 and 42277228)the Guangdong Basic and Applied Basic Research Foundation(No.2020A1515011560)the Science and Technology Planning Project of Guangzhou(Nos.202002030297 and 202002020072).
文摘Microplastics loaded with phenanthrene and derivatives are widely detected in aquatic environments,and the coating of natural minerals or organic macromolecules may change the environmental behavior of microplastics.In this study,three kinds of composites with different coverage were prepared by coating goethite on the surface of polyvinyl chloride microplastics to investigate the adsorption and desorption behavior of phenanthrene(PHE)and 1-hydroxyphenanthrene(1-OHPHE),and the effect of mucin on desorption was inves-tigated.The results showed that goethite promoted the adsorption of PHE and 1-OHPHE by increasing the specific surface area of the composites.With the increase of the cover de-gree,the adsorption of PHE decreased because of the decrease in hydrophobicity;while the adsorption of 1-OHPHE initially increased and then decreased with the contributions of hydrophobic interaction and hydrogen bond.The adsorption of 1-OHPHE could be influenced by the pH and ionic strength primarily through electrostatic interactions and Ca2+bridg-ing.The goethite significantly increased the desorption hysteresis for two chemicals due to the complicated pore structures and increased adsorption affinity.Mucin promoted the desorption of PHE through competitive adsorption,and inhibit the desorption of 1-OHPHE through hydrophobic interaction,hydrogen bonding and Ca2+bridging.This study elucidated the effects of natural minerals on the adsorption and desorption behavior of organic pollutants on microplastics,briefly discussed the effects of organic macromolecules on the desorption behavior of pollutants with different properties,and emphasized the different environmental behaviors of pollutants.
基金Supported by Zhaoqing University Innovation and Entrepreneurship Training Program for College Students (X202410580130).
文摘This paper summarizes the mechanisms and environmental effects of interactions between microplastics and surfactants: surfactants adsorb onto microplastics surfaces through hydrophobic interactions and electrostatic forces, changing their surface properties and transport behavior. In addition, microplastics act as carriers influencing surfactant distribution. Environmental factors (pH, ionic strength, etc. ) significantly regulate this process. Current research still has limitations in areas such as desorption kinetics and combined pollution effects, necessitating in-depth studies under environmentally relevant conditions to provide a basis for risk assessment.
基金funded by Indian Council of Agricultural Research,Ministry of Agriculture and Farmers Welfare,India(AGRIL.EDN/1/1/2022-EXAM CELL).
文摘Understanding how different vegetation-based restoration practices alter soil chemical and microbial characteristics is crucial,as restoration practices influence phosphorus(P)transformation and fractions and modify P adsorption behavior during the restoration process of degraded land.This study investigated the impacts of vegetation-based restoration practices on soil chemical and microbial parameters,P fractions,and patterns of P adsorption and desorption,and highlighted the combined influence on P availability.To evaluate the impact of vegetation-based restoration practices on P fractions and adsorption behavior in the semi-arid degraded land in India,this study compared three distinct tree-based restoration systems,including Leucaena leucocephala(Lam.)de Wit-based silviculture system(SCS),Acacia nilotica(L.)Willd.ex Delile-based silvopasture system(SPS),and Emblica officinalis Gaertn-based hortipasture system(HPS),with a natural grassland system(NGS)and a degraded fallow system(FS)as control.The soil samples across various soil depths(0-15,15-30,and 30-45 cm)were collected.The findings demonstrated that SCS,SPS,and HPS significantly improved soil organic carbon(SOC)and nutrient availability.Moreover,SCS and SPS resulted in increased microbial biomass phosphorus(MBP)content and phosphatase enzyme activity.The P fractionation analysis revealed that ferrum-associated phosphorus(Fe-P)was the major P fraction,followed by aluminum-associated phosphorus(Al-P),reflecting the dominance of ferrum(Fe)and aluminum(Al)oxides in the semi-arid degraded land.Compared with FS,vegetation-based restoration practices significantly increased various P fractions across soil depths.Additionally,P adsorption and desorption analysis indicated a lower adsorption capacity in tree-based restoration systems than in FS,with FS soils adsorbing higher P quantities in the adsorption phase but releasing less P during the desorption phase.This study revealed that degraded soils responded positively to ecological restoration in terms of P fraction and desorption behavior,influencing the resupply of P in restoration systems.Consequently,litter rich N-fixing tree-based restoration systems(i.e.,SCS and SPS)increased total phosphorus(TP)stock for plants and sustained the potential for long-term P supply in semi-arid ecosystems.With the widespread adoption of restoration practices across degraded landscapes,SCS and SPS would significantly contribute to soil restoration and improve productivity by maintaining the soil P supply in semi-arid ecosystems in India.
文摘[Objective]The research aimed to provide scientific reference for reasonable utilization of polyacrylamide(PAM).[Method]After PAM treatment,the soil aggregates were classified through dry sieve analysis and the adsorption capacity and desorption capacity of all soil aggregates to phosphorus at different phosphorus concentrations were analyzed.[Result] The phosphorus adsorption and desorption of soil sample treated by PAM declined. The amount of phosphorus adsorption increased with the increase of phosphorus concentration and this increase was fast in low phosphorus concentration area but slow in high phosphorus concentration area.At different phosphorus concentrations,adsorption showed a へ shape changing trend.The phosphorus adsorption was related to phosphorus concentration and the 2-3 mm aggregate had the highest desorption rate while 0.1-0.25 mm aggregate and 0.45-1 mm aggregate had lowest desorption rate.[Conclusion]The PAM treatment generated significant influence on phosphorus adsorption and analytic features of aggregate in all size fractions.
基金Project(41272287)supported by the National Natural Science Foundation of ChinaProject(13PJD029)supported by Shanghai Pujiang ProgramProject(SKLGDUEK1202)supported by State Key Laboratory for GeoMechanics and Deep Underground Engineering,China
文摘The Cr（III） desorption experiments of Gaomiaozi （GMZ） bentonite in aqueous solutions were performed. The variables affecting the desorption behaviors, such as contact time, concentration of the desorbent, pH value of the solution, temperature and desorption isotherms, were investigated by the batch experiments. The results show that the adsorbed Cr（III） on GMZ bentonite can be easily extracted by the desorbent. Kinetics examination shows that desorption is slower than adsorption, and the desorption rate increases with time and reaches the equilibrium after 3 h. The final desorption ratios of Cr（III） are 89.4%, 56.5%and 77.2%in the desorption solution with 0.1 mol/L HCl, 1 mol/L NaCl, and 1 mol/L CaCl2, respectively, and the concentration can promote the desorption progress. Furthermore, the results of successive regeneration cycles indicate that the bentonite has a good regeneration ability and reusability. The pH value is an important factor in the Cr（III） desorption from the GMZ bentonite. The results of adsorption and desorption isotherms show that both adsorption and desorption isotherms are consistent with the Freundlich equation. The comparison of adsorption and desorption isotherms implies that the adsorption/desorption hysteresis is negligible and the transport of Cr（III） in bentonite can be described by a reversible adsorption process.
基金National Natural Science Foundation of China (Grant No.30960515)Technological Innovation of Natural Science Project of Shihezi University(Grant No.ZRKX2008064 and No.ZRKX2008067)
文摘The adsorption and desorption of isoliquiritigenin and liquiritigenin to different types of carbon nanotubes （CNTs） were comparatively studied in this study. The pore structure, specific surface area, surface morphologies and functional groups of the CNTs were tested by N2 adsorption, scanning electron microscope （SEM） and infrared spectra （IR）. The investigation of dynamic adsorption, isothermal equilibrium adsorption and desorption of isoliquiritigenin and liquiritigenin to CNTs demonstrated that the adsorption amount on oxidized multi-walled carbon nanotubes （o-MWCNTs） was greater than that on raw multi-walled carbon nanotubes （r-MWCNTs）, especially the adsorption of isoliquiritigenin to o-MWCNTs. The data of equilibrium adsorption were better represented by the Freundlich isotherm model. In addition, the adsorbed amount per unit CNTs was decreased when the temperature got higher. From the results of isothermal equilibrium adsorption and desorption to CNTs, it could be inferred that o-MWCNTs had higher adsorption to isoliquiritigenin and liquiritigenin than r-MWCNTs. Additionally, o-MWCNTs had a better desorption efficiency to isoliquiritigenin and liquiritigenin （about 48.57% and 32.86%） than r-MWCNTs （about 24.56% and 17.46%）.
基金Supported by Science and Technology Research Project of Jiangxi Education Department(GJJ14289)Science and Technology Research Project of Environmental Protection Department of Jiangxi Province(JXHBKJ2013-4)Special Fund for Visiting Scholars from the Development Program for Middle-aged and Young Teachers in Colleges of Jiangxi Province(GJGH[2014]N0.15)
文摘[Objective] This study aimed to investigate the adsorption and desorption characteristics of cadmium and lead in typical paddy soils of Jiangxi Province. [Method] Gleyed paddy soil and waterloggogenic paddy soil were collected from Jiangxi Province and used as experimental materials to investigate single and com- petitive adsorption and desorption behaviors of cadmium and lead by batch equilib- rium method. The environmental risk of the presence of cadmium and lead in paddy soils was assessed using distribution coefficients. [Result] Under equal ratio condi- tions, the adsorption capacity of lead by two types of paddy soils was higher than that of cadmium, and the adsorption rate in waterloggogenic paddy soil was higher than that in gleyed paddy soil. The desorption capacity of cadmium by two types of paddy soils was higher than that of lead, and the desorption rate in gleyed paddy soil was higher than that in waterloggogenic paddy soil. Under competitive condi- tions, the adsorption capacity of cadmium and lead by paddy soils was significantly reduced compared with single ion system, while the desorption rate was remarkably improved. The potential environmental risk of cadmium contamination was greater than that of lead in paddy soils. Moreover, environmental risks of cadmium and lead were reduced with the increase of pH, which increased significantly under the coex- istence state. [Conclusion] In the coexistence of cadmium and lead, cadmium con- tamination should be controlled and avoided compared with lead contamination in paddy soils.
基金Supported by Program for Excellent Talents in Liaoning Higher Education Institutions(LJQ2012103)~~
文摘The adsorption and desorption kinetic of natural zeolite on NH4＋ was stud-ied by lab analysis. The results showed that the adsorption and desorption kinetic of natural zeolite on NH4＋ coincided with the first-order kinetics, modified Freundlich equation, parabolic diffusion model, and heterogeneous diffusion model. The desorp-tion of the adsorbed NH4＋ was far rapider than the adsorption, which can be fin-ished within 60 min.
基金supported by the Program for New Century Excellent Talents in University(NCET-12-0776)the National Natural Science Foundation of China(21507004)the Fundamental Research Funds for the Central Universities(FRF-TP-15-046A1)
文摘This work was undertaken to investigate the behaviors and kinetics of toluene adsorption and desorption on activated carbons with varying pore structure. Five kinds of activated carbon from different raw materials were selected. Adsorption isotherms and breakthrough curves for toluene were measured. Langmuir and Freundlich equations were fitted to the equilibrium data, and the Freundlich equation was more suitable for simulating toluene adsorption. The process consisted of monolayer, multilayer and partial active site adsorption types. The effect of the pore structure of the activated carbons on toluene adsorption capacity was investigated. The quasi-first-order model was more suitable for describing the process than the quasi-second-order model. The adsorption data was also modeled by the internal particle diffusion model and it was found that the adsorption process could be divided into three stages. In the external surface adsorption process, the rate depended on the specific surface area. During the particle diffusion stage, pore structure and volume were the main factors affecting adsorption rate. In the final equilibrium stage, the rate was determined by the ratio of meso-and macro-pores to total pore volume. The rate over the whole adsorption process was dominated by the toluene concentration. The desorption behavior of toluene on activated carbons was investigated,and the process was divided into heat and mass transfer parts corresponding to emission and diffusion mechanisms, respectively. Physical adsorption played the main role during the adsorption process.
基金the German Federal Ministry of Education and Research (BMBF) for funding the BonaR es project InnoS oil Phos (No. 031A558)
文摘Fourier-transform infrared（FT-IR） spectroscopic experiments were carried out during phosphate adsorption on highly crystalline gibbsite, poorly crystalline 2-line-ferrihydrite and amorphous iron–aluminum–hydroxide mixtures in the molar ratio 1：0, 10：1, 5：1, 1：1, 1：5, 1：10 and 0：1. The OH stretching vibrational bands were utilized to analyze changes in structural and surface OH groups during adsorption, because the position of characteristic P／O vibrational bands can shift depending on reaction conditions, pH or adsorbed phosphate content.Adsorption and desorption kinetics were studied at pH6 and different initial phosphate concentrations to achieve varying phosphate coverage on the mineral surfaces. For gibbsite the formation of AlHPO4 and Al2HPO4 can be assumed, while for ferrihydrite, a FeHPO4 or Fe2PO4 complex and the precipitation of FePO4 with longer equilibration time were proposed.Fe2HPO4 or a Fe2PO4 surface complex was deduced for Fe-hydroxides, an AlH2PO4 surface complex was identified for Al-hydroxide, and both displayed either hydrogen bonds to neighboring hydroxyl groups or hydrogen bonds to outer-sphere complexes. Fe：Al-hydroxide mixtures with high Al ratios showed a low phosphate desorption rate, while ferrihydrite and the Fe：Al-hydroxide mixtures with high Fe ratios had almost negligible desorption rates. It was concluded that within the weakly associated amorphous FeO（OH） materials, FePO4 precipitated, which was bound by outer-sphere hydrogen bonds. With high Al ratios, desorption increased, which indicated weaker phosphate binding of both inner-sphere and outer-sphere complexes and hence, either no or minor quantities of precipitate. Ferrihydrite showed a more rigid structure and a lower extent of precipitation compared to amorphous Fe-hydroxide.
文摘A novel amphoteric granular lignin adsorbent(AGLA) was prepared using magnesium lignosulfonate as a raw material which was provided by a straw sulfite pulp mill in Guangdong Province, China. A reactive dye(red K-3B) was used as an adsorbate to investigate the adsorption behavior by static and mobile ways. The removal of reactive red K-3B was found to be initially pH and concentration dependent. Moreover, an increase of solution temperature ranging from 5℃ to 60℃ helped to enhance the rate of intraparticle diffusion of adsorbate and changes in the size of the pores of the adsorbent and thus to reduce the adsorption time. The total breakthrough adsorption capacity was 531 mg/g, and the saturated adsorption capacity was 560 mg/g, which prevailed over the activated carbons evidently. The reactive red K-3B adsorbed on AGLA could be recovered with a mixture of alcohol, NaCl and HCl aqueous solutions. The recovery percentage could reach 92.4%.
基金the National Natural Sci-ence Foundation of China (No. 40673063, 40573065)
文摘Effects of dissolved organic matter (DOM) on adsorption and desorption of Hg were investigated in two kinds of soils, Xanthi-Udic Ferralosols (XUF) and Typic Purpli-Udic Cambosols (TPUC). The DOM was obtained from humus soil (DOMH), rice straw (DOMR), and pig manure (DOMP). The presence of DOM obviously reduced Hg maximum adsorption capacity with up to 40% decreases over the control, being an order of DOMH (250.00 mg/kg)< DOMR (303.03 mg/kg) < DOMP (322.58 mg/kg) < CK (control 416.67 mg/kg) for the...
基金supported by the National Nature Science Foundation of China (No. 20807010)the Program for New Century Excellent Talents in University (No. NCET-09-0256)+1 种基金the Specialized Research Fund for the Doctoral Program of Higher Education (No. 200801411111)the National High Technology Research and Development Program (863) of China (No. 2009AA062604)
文摘Four different types of adsorbents, SBA-15, MCM-41, NaY and SiO2, were used to study the dynamic adsorption/desorption of toluene. To further investigate the influence of pore structure on its adsorption performance, two SBA-15 samples with different microspores were also selected. It is shown that microporous material NaY has the largest adsorption capacity of 0.2873 mL/g, and the amorphous SiO2 exhibits the least capacity of 0.1003 mL/g. MCM-41 also shows a lower break through capacity in spite of the relatively small pore diameter, because it can not provide the necessary small geometric confinement for the tiny adsorbates. However, the mesoporous SBA-15 silica with certain micropore volume shows relatively higher adsorption capacity than that of MCM-41 silica. The presence of micropores directly leads to an increase in the dynamic adsorption capacity of toluene. Although NaY has the highest adsorption capacity for toluene, its complete desorption temperature for toluene is high （〉 350°C）, which limits its wide application. On the contrary, mesoporous silica materials exhibits a good desorption performance for volatile organic compounds at lower temperatures. Among these materials mesoporous SBA-15 samples, with a larger amount micropores and a lower desorption temperature, are a potentially interesting adsorbent for the removal of volatile organic compounds. This behavior should been related with the best synergetic effect of mesopores and micropores.
基金supported by the Knowledge Innovation Program Foundation of the Chinese Academy of Sciences(No. KZCX2-YW-Q10-3,ISSASIP0713)
文摘The adsorption and desorption of Cu（Ⅱ） and Pb（Ⅱ） on upland red soil,and paddy soils which were originated from the upland soil and cultivated for 8,15,35 and 85 years,were investigated using the batch method.The study showed that the organic matter content and cation exchange capacity （CEC） of the soils are important factors controlling the adsorption and desorption of Cu（Ⅱ） and Pb（Ⅱ）.The 15-Year paddy soil had the highest adsorption capacity for Pb（Ⅱ）,followed by the 35-Year paddy soil.Both the 35-Year paddy soil and 15-Year paddy soil adsorbed more Cu（Ⅱ） than the upland soil and other paddy soils.The 15-Year paddy soils exhibited the highest desorption percentage for both Cu（Ⅱ） and Pb（Ⅱ）.These results are consistent with the trend for the CEC of the soils tested.The high soil CEC contributes not only to the adsorption of Cu（Ⅱ） and Pb（Ⅱ） but also to the electrostatic adsorption of the two heavy metals by the soils.Lower desorption percentages for Cu（Ⅱ） （36.7% to 42.2%） and Pb（Ⅱ） （50.4% to 57.9%） were observed for the 85-Year paddy soil.The highest content of organic matter in the soil was responsible for the low desorption percentages for the two metals because the formation of the complexes between the organic matter and the metals could increase the stability of the heavy metals in the soils.
基金supported by the National Basic Research Program (973) of China (No.2009CB119200)the Chongqing Natural Science Foundation (CSTC) (No.2009BA1042)the Program for Changjiang Scholars and Innovative Research Team in University (No.IRT0976)
文摘Monosulfuron-ester is a new,low rate,sulfonylurea herbicide that is being promoted for annual broadleaf and gramineal weed control;however,there is a lack of published information on its behavior in soils.The adsorption and desorption of monosulfuronester by seven type soils were measured using a batch equilibrium technique.The results showed that the Freundlich equation fitted its adsorption and desorption well,and the Freundlich constant values （K f-ads ） ranged from 0.88 to 5.66.Adsorption isotherms were nonlinear with 1/n f-ads values 1.Soil pH,organic matter （OM）,and clay content were the main factors influencing its adsorption and desorption.Adsorption and desorption were negatively correlated with pH 4.0–8.0 while positively correlated with OM and clay content.The adsorption of monosulfuron-ester was mainly a physical process,because its free energy （？G） in seven soils was less than 40 kJ/mol.Monosulfuron-ester adsorption by three soils increased with increasing CaCl 2 concentration using CaCl 2 as a background electrolyte.Monosulfuron-ester desorption was hysteretic in all tested soils.
文摘The behavior of herbicide acetochlor adsorption desorption to soil in the presence of humic acid (HA), anionic surfactant sodium dodecylbenzene sulfonate (SDBS), cationic surfactant hexadecyltrimethyl ammonium bromide (HDAB) and NH 4NO 3 as a chemical fertilizer was studied. Observed acetochlor adsorption isotherm were well described using Freundlich isotherm equation, from which the desorption isotherm equation has been deduced. The deduced equation can more directly describe acetochlor desorption process. The results showed that the enhance of acetochlor adsorption capacity by solid HA was greater than by soluble HA. The presence of NH 4NO 3 can slightly enhance acetochlor adsorption to soil by comparison with that measured in NH 4NO 3 free solution. In soil water system, surfactant acetochlor interaction is very complex, and the surfactant adsorptions as well as acetochlor adsorption need to be considered. When acetochlor soil suspensions contained lower concentration SDBS or HDAB (40 mg/L), K f for acetochlor adsorption was decreased in comparison to that measured in SDBS or HDAB free solution. When acetochlor soil suspensions contained higher concentration SDBS or HDAB (corresponding 1400 mg/L or 200 mg/L), K f for acetochlor adsorption was increased in comparison to that measured in SDBS or HDAB free solution.
基金Project supported by the National Basic Research Program of China(Grant No.2011CB201202)
文摘Effects of particle size on CH4 and CO2adsorption and desorption characteristics of coals are investigated at 308 K and pressures up to 5.0 MPa.The gas adsorption and desorption isotherms of coals with particle sizes ranging from 250 μm to 840 μm are measured via the volumetric method,and the Langmuir model is used to analyse the experimental results.Coal particle size is found to have an obvious effect on the coal pore structure.With the decrease of coal particle size in the process of grinding,the pore accessibility of the coal,including the specific surface area and pore volume,increases.Hence,coal with smaller particle size has higher specific surface area and higher pore volume.The ability of adsorption was highly related to the pore structure of coal,and coal particle size has a significant influence on coal adsorption/desorption characteristics,including adsorption capacity and desorption hysteresis for CH4 and CO2,i.e.,coal with a smaller particle size achieves higher adsorption capacity,while the sample with a larger particle size has lower adsorption capacity.Further,coal with larger particle size is also found to have relatively large desorption hysteresis.In addition,dynamic adsorption performances of the samples are carried out at 298 K and at pressures of 0.1 MPa and 0.5 MPa,respectively,and the results indicate that with the increase of particle size,the difference between CO2 and CH4adsorption capacities of the samples decreases.
基金supported by the National Natural Science Foundation of China (No. 41171248,40810180)the Ministry of Environmental Protection Special Funds for Scientific Research on Public Causes (No. 2010467016)
文摘Diphenylarsinic acid （DPAA） is formed during the leakage of aromatic arsenic chemical weapons in soils, is persistent in nature, and results in arsenic contamination in the field. The adsorption and desorption characteristics of DPAA were investigated in two typical Chinese soils, an Acrisol （a variable-charge soil） and a Phaeozem （a constant-charge soil）. Their thermodynamics and some of the factors influencing them （i.e., initial pH value, ionic strength and phosphate） were also evaluated using the batch method in order to understand the environmental fate of DPAA in soils. The results indicate that Acrisol had a stronger adsorption capacity for DPAA than Phaeozem. Soil DPAA adsorption was a spontaneous and endothermic process and the amount of DPAA adsorbed was affected significantly by variation in soil pH and phosphate. In contrast, soil organic matter and ionic strength had no significant effect on adsorption. This suggests that DPAA adsorption may be due to specific adsorption on soil mineral surfaces. Therefore, monitoring the fate of DPAA in soils is recommended in areas contaminated by leakage from chemical weapons.
文摘In many sources of volatile organic compounds (VOCs), large amounts of water vapor come from the air and the reactors. The relative humidity (RH) of exhaust gas is normally >60% and is supersaturated. Maintaining the property of adsorbent on VOCs in a highly humid gas stream is a serious industrial problem. In this study, the adsorption/desorption behavior of toluene in a micro-mesoporous polymeric resin was investigated in a highly humid environment to explore the influence of abound water vapor on resin adsorption and regeneration. This resin could selectively adsorb toluene at an RH of 80%, and its adsorption property was unaffected by the presence of water vapor. In the case of humidity saturation, the resin displayed a high adsorption capacity at a moisture content of <30%. Therefore, the polymer resin is an excellent water-resistant adsorbent of VOCs. In the regenerative experiment, the resin maintained its original adsorption capability after four adsorption/ desorption cycles of toluene purging with nitrogen gas at 120℃. The resin exhibited excellent regeneration performance at high humidity.
