Effect of extracellular polymeric substances on the phosphorus adsorption characteristics of sediment particles

Extracellular polymeric substances (EPS) have a great impact on the characteristics of sediment particles and their environmental effects in hydro-environmental systems, yet little effort has been made to study the considerable variability in the element adsorption process of sediment particles caused by EPS. Understanding the variability of the adsorption characteristics of sediment particles associated with EPS and quantifying the scale of the adsorption isotherm parameters are important for understanding how EPS mediate sediment properties and environmental factors. In this paper, isothermal equilibrium adsorption experiments are done on phosphorus to study the influence of EPS on the adsorption characteristics of sediment particles, and the Langmuir adsorption isotherm is applied to analyze the adsorption rule of sediment particles under the impact of EPS. The current research demonstrates that significant differences will take place in the adsorption characteristics of sediments coated with EPS at different development phases and the phosphorus adsorption capacity of sediment particles increases with the growth of EPS. The difference in the adsorption percentage between sediment particles coated with EPS of 0 and 6 weeks growth time is about 42%–60% for different initial aqueous phosphorus concentration. A formula describing the adsorption isotherm parameter of the maximum material (element) adsorption capacity of sediment particles change over time is further proposed based on the experimental data. The current study provides some evidence for the interaction of sediment particles, EPS, and adsorbed elements in the water environment.     

Batch and Continuous Design of a Full‐Scale Treatment Facility for Removing Dissolved Natural Organic Matter

Batch and continuous flow adsorption experiments are carried out and the design of a full‐scale facility for removing dissolved natural organic matter (DNOM) from Catalan Lakewater is demonstrated. The adsorption efficiency is proportional to the temperature and the amount of adsorbent unlike pH increase. The highest DNOM removal rate is obtained at 35 °C, pH 4, and an adsorbent amount of 0.8 g L^?1. Optimum contact time for batch studies is 60 min at equilibrium. Correlation constants (r) of Langmuir and Freundlich isotherms are 0.8905 and 0.9739, respectively. Based on the Freundlich isotherm, the highest adsorption capacity (q_max) obtained is 2.44 and 6.01 mg DNOM/g granulated activated carbon (GAC) for raw and enriched water, respectively. Consequently, the effects of adsorbent amount, bed depth, empty bed contact time, and organic loading on removal performance are investigated in the rapid small‐scale column test (RSSCT) columns. The targeted effluent concentration of 1 mg DNOM/L can easily be achieved in the columns. At the design capacity of the facility, 15 adsorption columns with dimensions of 7 m height, 4.33 m diameter, and 22 days of operation cycle are required to remove DNOM from raw water.     

有机质对城市污染河道沉积物铵态氮吸附-解吸的影响

采集污染程度不同的城市河道沉积物(通吕运河、濠河和通甲河),在分析H2O2对沉积物有机质和铵态氮影响的基础上,分析沉积物在去除有机质前后铵态氮释放动力学和吸附热力学过程,研究城市污染河道沉积物有机质对铵态氮吸附-解吸的影响.结果表明:单位体积H2O2对有机质去除率随H2O2使用量增多而降低;去除有机质后,沉积物铵态氮含量显著增加,通吕运河、濠河和通甲河铵态氮最大含量分别是有机质去除前的4.16、3.55和2.85倍;沉积物对铵态氮的饱和吸附量随有机质含量减少而下降;沉积物铵态氮释放过程均表现为先快速释放,后减缓至平衡过程;去除有机质后,随着有机质含量的减少,沉积物铵态氮的最大释放量呈增大趋势;沉积物有机质和铵态氮含量是影响沉积物铵态氮释放的主要因素.     

Characteristics of micro-interface adsorption kinetics between sediments and Cu ions

This work investigates the adsorption of Cu ions in sediments by conducting batch experiments,including isothermal experiments and adsorption kinetics experiments.Data from isothermal experiments were analyzed using the Langmuir,Freundlich and Temkin models,and the experimental kinetic data were fit using pseudo-first-order,pseudo-second-order,Elovich,liquid film diffusion and intra-particle diffusion models.The Langmuir model resulted in the best fit for the equilibrium data,which indicated that the adsorption capacity of Cu ions on the sediment was 1.0403 mg g-1 with a KL value of 4.2877 L mg-1.The Freundlich and Temkin models also provided good fits,and the nF and A values were 3.8565 and 66.9964 L mg-1,respectively,indicating stronger adsorption intensities and adsorption energies between the Cu ions and the sediment.Compared with the pseudo-first-order and Elovich models,the pseudo-second-order model was more appropriate for describing the adsorption kinetics,indicating the chemisorption nature of adsorption.The adsorption kinetic process can be divided into film diffusion,pore diffusion and adsorption reactions.The controlling step for the adsorption kinetics changed with the development of the adsorption process.The entire adsorption process took 180 min.Film diffusion was the controlling step for the first 20 min.During the 20 to 60 min period,the pore diffusion gradually increased and the film diffusion decreased so that both phenomena coexisted.Pore diffusion was the controlling step during the 60-180 min period.     

硫铝酸盐水泥去除微污染水体中磷的性能及机理

微污染湖泊、水库等水体中磷的去除已成为水质研究的主要方向.磷是造成水体富营养化的关键因素,其浓度较低时即可导致水体富营养化与水华的发生,许多除磷方法对低浓度磷的去除效果不佳.因此,我们从22种天然矿物、火山灰质材料和水硬性材料中,筛选出了能高效去除低浓度磷的硫铝酸盐水泥(代号R.SAC 42.5,简称R),该材料在中性...     

Spatiotemporal variations of internal P-loading and the related mechanisms in the large shallow Lake Chaohu

Spatiotemporal variations of P species and adsorption behavior in water column, interstitial water, and sediments were investigated in the large shallow eutrophic Lake Chaohu. Ortho-phosphate (Ortho-P) and total phosphorus (TP) concentrations were significantly higher in the western part than in the eastern part of the lake, due to different nutrient inputs from the surrounding rivers. Moreover, paniculate phosphorus (PP) concentration was in a similar spatial pattern to Ortho-P and TP concentrations, and also showed significantly positive correlation with the biomass of Microcystis, indicating more uptake and store of phosphorus by Microcystis than by other algae. Increase of pH and intensive utilization of P by phytoplankton were the main factors promoting P (especially Fe-P) release from the sediment to interstitial water during the cyanobacterial blooms in Lake Chaohu. Spatial dynamics in TP concentration, P species and adsorption behavior of the sediment, coupled with the statistical analyses, suggested that the spatial heterogeneity of P contents in the sediment was influenced by various factors, e.g. human activities, soil geochemistry and mineral composition. In spite of similar TP contents in the sediments, increase in proportion of Fe-P concentration in the sediment may result in a high risk of P release.     

Adsorption of Selenium Using Bagasse Fly Ash

The present work involves the study of Se(IV) adsorption onto bagasse fly ash. The adsorbents were coated with a ferric chloride solution for the effective removal of selenium. The physico‐chemical characterization of the adsorbent was carried out using standard methods, e. g., proximate analysis, scanning electron microscopy, Fourier transform infrared spectroscopy, thermo‐gravimetric analysis and differential thermal analysis. Batch experiments were carried out to determine the effect of various parameters such as adsorbent dose, initial pH, contact time, and temperature on the adsorption process. Results obtained from these studies were analyzed using various kinetic models and isotherms. Se(IV) adsorption onto adsorbent was high at low pH values, and decreased with an increase in initial pH. A temperature study showed that the uptake of Se(IV) was greatest at 293 K, within the temperature range studied. The parameters of pseudo first order, pseudo second order, and Weber‐Morris intra‐particle kinetic models were determined. Equilibrium isotherms were analyzed using Langmuir, Freundlich, and Temkin isotherms. Error analyses were also carried out using hybrid fractional error function and Marquardt's percent standard deviation.     

Spatiotemporal variations of internal P-loading and the related mechanisms in the large shallow Lake Chaohu

Spatiotemporal variations of P species and adsorption behavior in water column, interstitial water, and sediments were investigated in the large shallow eutrophic Lake Chaohu. Orthophosphate (Ortho-P) and total phosphorus (TP) concentrations were significantly higher in the western part than in the eastern part of the lake, due to different nutrient inputs from the surrounding rivers. Moreover, particulate phosphorus (PP) concentration was in a similar spatial pattern to Ortho-P and TP concentrations, and also showed significantly positive correlation with the biomass of Microcystis, indicating more uptake and store of phosphorus by Microcystis than by other algae. Increase of pH and intensive utilization of P by phytoplankton were the main factors promoting P (especially Fe-P) release from the sediment to interstitial water during the cyanobacterial blooms in Lake Chaohu. Spatial dynamics in TP concentration, P species and adsorption behavior of the sediment, coupled with the statistical analyses, suggested that the spatial heterogeneity of P contents in the sediment was influenced by various factors, e.g. human activities, soil geochemistry and mineral composition. In spite of similar TP contents in the sediments, increase in proportion of Fe-P concentration in the sediment may result in a high risk of P release.     

Removal of EDTA from Aqueous Solutions Using Activated Carbon Prepared from Rubber Wood Sawdust: Kinetic and Equilibrium Modeling

Adsorptive removal of EDTA (ethylenediaminetetraacetic acid) from aqueous solution was studied using steam pyrolyzed activated carbon. Rubber wood sawdust, obtained from a local timber facility at Kodangavila, Trivandrum, Kerala, India was used as the precursor for the production of the activated carbon. Batch adsorption experiments were employed to monitor and optimize the removal process. The experimental parameters, i. e., solution pH, agitation time, initial EDTA concentration and adsorbent dosage, affecting the adsorption of EDTA onto sawdust activated carbon (SDAC) were optimized. The inner core mechanism for the interaction between EDTA and SDAC, which resulted in the adsorption process, was also discussed. The change in amount of EDTA adsorbed onto SDAC and CAC (commercial activated carbon) was compared over a wide range of pH (2.0–8.0). The maximum removal of EDTA took place in the pH range of 4.0–6.0 for SDAC and 5.0–5.5 for CAC, which demonstrates the effectiveness of the former adsorbent. Kinetic as well as equilibrium studies were performed to determine the rate constant and adsorption capacity, respectively. The adsorption kinetic data was fitted with pseudo‐first‐order kinetics and the equilibrium data was shown to follow the Langmuir isotherm model. These observations explain the formation of a monolayer of EDTA on the surface of SDAC as confirmed by the slow approach to equilibrium after 4 h of contact time. The adsorption capacity of SDAC for the removal of EDTA was 0.526 mmol/g and is seen to be greater than that of CAC and other reported adsorbents (0.193–0.439 mmol/g). Finally, it is clear that the production of steam pyrolyzed activated carbon in the presence of K₂CO₃ greatly enhanced EDTA removal and resulted in a product with possible commercial value for wastewater treatment strategies.     

Adsorption of cobalt by using inorganic components of sediment samples from water bodies

The adsorption of cobalt ions was evaluated using sediment samples from water bodies to investigate the adsorption properties of sediment and the behavior of these natural materials in the presence of nuclear and industrial waste.The two sediments(S1 and S2)were treated to eliminate humic and fulvic acids and then they were characterized by several techniques.The minerals found in both the sediments(X-ray diffraction)were quartz and albite;plus,goethite and muscovite in S1,and kaolinite and montmorillonite in S2.Point of zero charge(PZC)of S1 and S2 was 6.00 and 5.22,respectively.The specific area of S1(63.3 m²/g)is higher than S2(1.5 m²/g).Adsorption kinetics data for S1 and S2 were best fitted to the pseudo second-order model.The removal efficiency of S1 for cobalt was 96%with an adsorption capacity(qe)of 0.93 mg/g,and for S2 was 45%with a qeof 0.40 mg/g.The experimental data of the adsorption isotherms were adjusted to Langmuir and Freundlich models for S1 and S2,respectively.The thermodynamic parameters(enthalpy,entropy,and Gibb’s free energy)indicated that the adsorption processes were endothermic,spontaneous,and chemisorption mechanism.The results show that the adsorption capacities of the sediments depend on their composition.These water sediments have important adsorption properties for cobalt,and they can be used in the treatment of nuclear and industrial aqueous wastes.     

Isotherm Study of Phosphorus Uptake from Aqueous Solution Using Aluminum Oxide

Aluminum oxide, which could be an alternative filter media for phosphorus uptake from aqueous solution, was selected as an adsorbent for the isotherm study of phosphorus uptake from aqueous solution. Batch method was adopted to investigate the adsorption behavior of phosphorus onto aluminum oxide. The Langmuir, Freundlich, and Redlich–Peterson isotherms were used to analyze the experimental data by both the linear and nonlinear regression methods. The adsorption experiment was conducted at various temperatures, to choose the appropriate method and obtain the creditable adsorption parameters for phosphorus uptake studies. The results indicated that the nonlinear regression method might be a better way to compare the best‐fitting isotherm and obtain the parameters for the adsorption of phosphorus onto aluminum oxide. Both the Redlich–Peterson and the Freundlich isotherms have high coefficients of determination for the adsorption of phosphorus onto aluminum oxide at various temperatures. In addition, a new relationship between the Redlich–Peterson and the Freundlich isotherm parameters was presented.     

Adsorption Characteristics of Reactive Black 5 from Aqueous Solution onto Chitosan

Adsorption of reactive black 5 (RB5) from aqueous solution onto chitosan was investigated in a batch system. The effects of solution pH, initial dye concentration, and temperature were studied. Adsorption data obtained from different batch experiments were modeled using both pseudo first‐ and second‐order kinetic equations. The equilibrium adsorption data were fitted to the Freundlich, Tempkin, and Langmuir isotherms over a dye concentration range of 45–100 µmol/L. The best results were achieved with the pseudo second‐order kinetic and Langmuir isotherm equilibrium models, respectively. The equilibrium adsorption capacity (q_e) was increased with increasing the initial dye concentration and solution temperature, and decreasing solution pH. The chitosan flakes for the adsorption of the dye was regenerated efficiently through the alkaline solution and was then reused for dye removal. The activation energy (E_a) of sorption kinetics was estimated to be 13.88 kJ/mol. Thermodynamic parameters such as changes in free energy (ΔG), enthalpy (ΔH), and entropy (ΔS) were evaluated by applying the van't Hoff equation. The thermodynamics of reactive dye adsorption by chitosan indicates its spontaneous and endothermic nature.     

Adsorption Performance and Mechanism in Binding of Azo Dye by Raw Bentonite

The adsorption behavior of methyl orange (MO) from aqueous solution onto raw bentonite (RB) sample was investigated as a function of parameters such as pH, inorganic anion, contact time, and temperature. The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms. Langmuir adsorption capacity was found to be 34.34 mg/g at pH 4.0. The pseudo‐first‐order, pseudo‐second‐order kinetic, and the intra‐particle diffusion models were used to describe the kinetic data. The values of the energy (E_a), enthalpy (ΔH^≠), and entropy of activation (ΔS^≠) were calculated as 38.62 kJ/mol, 36.04 kJ/mol, and ?150.05 J/mol K, respectively, at pH 4.0.     

Separation of Vanillin and Syringaldehyde from Oxygen Delignification Spent Liquor by Macroporous Resin Adsorption

This paper reports on an approach for separating vanillin and syringaldehyde (VSA) from oxygen delignification spent liquor using non‐polar macroporous resin. The effects of temperature and pH on the adsorption isotherms were studied. The adsorption capacity and adsorption equilibrium constant were obtained using the Langmuir adsorption model at pH<4.5, where the ionization of the VSA to ionic forms was negligible. The standard enthalpy change was calculated using the van't Hoff equation and clearly showed that the adsorption is an exothermic process. The effect of pH on the adsorption isotherm is well‐described by a modified Langmuir model and shows that the adsorption equilibrium constant decreases significantly with the increasing pH. The VSA adsorbed on macroporous resin was eluted by ethyl ether. The separated VSA contained 37.51% vanillin, 31.88% syringaldehyde. The recoveries of VSA were 96.2 and 94.7%, respectively.     

Adsorption Characteristics of Rhodamine B from Aqueous Solution onto Baryte

Batch sorption experiments were carried out for the adsorption of the basic dye Rhodamine B from aqueous solution using baryte as the adsorbent. The effect of adsorbent dosage, temperature, initial dye concentration and pH were studied. Adsorption data were modeled using first and second order kinetic equations and the intra particle diffusion model. Kinetic studies showed that the adsorption process followed second order rate kinetics with an average rate constant of 0.05458 g mg^–1 min^–1. Dye adsorption equilibrium was attained rapidly after 30 min of contact time. The equilibrium data was fitted to the Langmuir, Freundlich and Tempkin isotherms over a dye concentration range of 50–250 mg/L. The adsorption thermodynamic parameters showed that adsorption was an exothermic, spontaneous and less ordered arrangement process. The adsorbent, baryte, was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The results showed that baryte has good potential for the removal of Rhodamine B from dilute aqueous solution.     

Experimental and Isothermal Studies on Sorption of Congo Red by Modified Mycelial Biomass of Wood‐rotting Fungus

Batch biosorption experiments were carried out for the removal of Congo red from aqueous solution using native and pretreated mycelial pellets/biomass of Trametes versicolor. The effect of process parameters such as contact time, dye concentration, and pH on the extent of Congo red biosorption has been investigated. Higher dye concentrations resulted in lower biosorption. Increases in biomass dosage led to increases in the levels of biosorption. Biosorption kinetics and equilibrium data are essential basic requirements to develop an effective and accurate design model for the removal of the dye. A kinetic study showed that the biosorption of the dye on fungal biomass was a gradual process. Pseudo‐first‐order, pseudo‐second‐order, and Bangham's model were used to fit the experimental data. The results of the kinetic studies showed that the second‐order kinetic model fitted well for the present experimental data. Equilibrium isotherms were analyzed by Langmuir, Freundlich, Dubnin‐Radushkevich, and Temkin isotherms. The biosorption equilibrium data obeyed the Langmuir and Temkin isotherms well. Acidic pH was favorable for the biosorption of the dye. Studies on the pH effect and desorption show that chemisorption seems to play a major role in the biosorption process. Among the native and pretreated biomass studied, autoclaved biomass showed a better biosorption capacity.     

Development of Polymeric and Polymer‐Based Hybrid Adsorbents for Chromium Removal from Aqueous Solution

Ferric oxide‐loaded hybrid sorbents are environmentally benign and exhibit sorption behaviors for chromium removal from waters. In the current study, glycidyl methacrylate‐based polymer (GMD) and nanosized ferric oxide loaded glycidyl methacrylate‐based polymer (GMDFe) were prepared and assayed to examine the effect of ferric oxide loading on chromium sorption from aqueous solution for the first time from the equilibrium and kinetic points of view. The experimental equilibrium data, suitably fitted by the Langmuir and Freundlich isotherms, have shown that ferric oxide loaded hybrid sorbent exhibits higher adsorption capacity than glycidyl methacrylate‐based polymer (GMD). The Langmuir isotherm model was found to be the most suitable one for the Cr(VI) adsorption. The maximum adsorption capacities of GMD and GMDFe sorbents were determined at pH 4 as 109.54 and 157.52 mg/g, respectively. A series of column experiments was carried out to determine the breakthrough curves. The column was regenerated by eluting Cr(VI) using NaOH (10% w/v) solution after adsorption studies.     

Investigation of Biosorption Behavior of Methylene Blue on Pleurotus ostreatus (Jacq.) P. Kumm.

The effect of varying parameters such as dye concentration, adsorbent dose, pH and temperature on the adsorption capacity of Pleurotus ostreatus is investigated. The commonly available white rot fungus Pleurotus ostreatus is investigated as a viable biomaterial for the biological treatment of synthetic basic methylene blue effluents. The results obtained from the batch experiments reveal the ability of the fungus to remove methylene blue. The performance is dependent on the dye concentration, pH, and fungal biomass. The equilibrium and kinetics of adsorption are investigated and the Langmuir equation is used to fit the equilibrium isotherm. The adsorption isotherm of methylene blue follows only the Langmuir model with a correlation coefficient of ca. 0.96–0.99. The maximum adsorption capacity is ca. 70 mg of dye per g of dry fungus at pH 11, 70 mg L^–1 dye, and 0.1 g L^–1 fungus concentration, respectively. This study demonstrates that the fungus could be used as an effective biosorbent for the treatment of dye‐containing wastewater streams.     

Organic diagenesis in sediment and its impact on the adsorption of bisphenol A and nonylphenol onto marine sediment

Hydrophobic organic contaminants in marine water are mostly adsorbed onto (partitioned into) sediment organic matter (SOM). To study the impact of SOM diagenesis on sediment adsorption properties, artificial sediment with rich SOM content was incubated for more than 120 days. The sediment was sampled every week, and batch sediment adsorption tests were conducted with bisphenol A (BPA) and nonylphenol (NP) as the model pollutants. The results show that the amount of organic matter loaded in the sediment decreased by nearly 80% during incubation. For the incubated sediment, the BPA partition coefficient, Kd, decreased whereas the organic normalized partition coefficient, Koc, more than doubled. The experiments with NP show an even greater increase in Koc. Organic matter diagenesis shows a profound effect on the adsorption behavior of sediment, as the SOM residue has an increasing affinity and partition capacity for organic contaminants.