Biosorption characteristics of unicellular green alga Chlorella sorokiniana immobilized in loofa sponge for removal of Cr(Ⅲ)

Loofa sponge (LS) immobilized biomass of Chlorella sorokiniana (LSIBCS), isolated from industrial wastewater, was investigated as a new biosorbent for the removal of Cr(Ⅲ) from aqueous solution. A comparison of the biosorption of Cr(Ⅲ) by LSIBCS and free biomass of C. sorokiniana (FBCS) from 10-300 mg Cr(Ⅲ)/L aqueous solutions showed an increase in uptake of 17.79% when the microalgal biomass was immobilized onto loofa sponge. Maximum biosorption capacity for LSIBCS and FBCS was found to be 69.26 and 58.80 mg Cr(Ⅲ)/g biosorbent, respectively, whereas the amount of Cr(Ⅲ) ions adsorbed onto naked LS was 4.97 mg/g. The kinetics of Cr(Ⅲ) biosorption was extremely rapid and equilibrium was established in about 15 and 20 min by LSIBCS and FBCS,respectively. The biosorption equilibrium was well defined by Langmuir adsorption isotherm model. The biosorption kinetics followed the pseudo-second order kinetic model. The biosorption was found to be pH dependent and the maximum sorption occurred at the solution pH 4.0. Desorption studies showed that 98% of the adsorbed Cr(Ⅲ) could be desorbed with 0.1 mol/L HNO3, while other desorbing agents were less effective in the order: EDTA ＞ H2SO4 ＞ CH3COOH ＞ HCl. The regenerated LSIBCS retained 92.68% of the initial Cr(Ⅲ) binding capacity up to five cycles of reuse in continuous flow-fixed bed columns. The study revealed that LSIBCS could be used as an effective biosorbent for the removal of Cr(Ⅲ) from wastewater.     

New insight into adsorption characteristics and mechanisms of the biosorbent from waste activated sludge for heavy metals

The adsorption characteristics and mechanisms of the biosorbent from waste activated sludge were investigated by adsorbing Pb2+and Zn2+in aqueous single-metal solutions. A p H value of the metal solutions at 6.0 was beneficial to the high adsorption quantity of the biosorbent. The optimal mass ratio of the biosorbent to metal ions was found to be 2. A higher adsorption quantity of the biosorbent was achieved by keeping the reaction temperature below 55°C. Response surface methodology was applied to optimize the biosorption processes, and the developed mathematical equations showed high determination coefficients(above 0.99 for both metal ions) and insignificant lack of fit(p = 0.0838 and 0.0782 for Pb2+and Zn2+, respectively). Atomic force microscopy analyses suggested that the metal elements were adsorbed onto the biosorbent surface via electrostatic interaction. X-ray photoelectron spectroscopy analyses indicated the presence of complexation(between –NH2,-CN and metal ions) and ion-exchange(between –COOH and metal ions). The adsorption mechanisms could be the combined action of electrostatic interaction, complexation and ion-exchange between functional groups and metal ions.     

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

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

Immobilization study of biosorption of heavy metal ions onto activated sludge

Activated sludge was immobilized into Ca-alginate beads via entrapment, and biosorption of three heavy metal ions, copper(Ⅱ), zinc(Ⅱ), and chromimum(Ⅱ), from aqueous solution in the concentration range of 10-100 mg/L was studied by using both entrapped activated sludge and inactivated free biomass at pH≤5. A biphasic metal adsorption pattern was observed in all immobilized biomass experiments. The biosorption of metal ions by the biosorbents increased with the initial concentration increased in the medium. The adsorption rate of immobilized pre-treated activated sludge(PAS) was much lower than that of free PAS due to the increase in mass transfer resistance resulting from the polymeric matrix. Biosorption equilibrium of beads was established in about 20 h and the adsorbed heavy metal ions did not change further with time. No significant effect of temperature was observed in the test for free biomass while immobilized PAS appeared to be strong temperature dependent in the test range of 10 and 40℃.Besides, the content of activated sludge in the calcium alginate bead has an influence on the uptake of heavy metals. The sorption equilibrium was well modeled by Langmuir isotherm, implying monomolecular adsorption mechanism. Carboxyl group in cell wall played an important role in surface adsorption of heavy metal ions on PAS.     

Copper biosorption on immobilized seaweed biomass： Column breakthrough characteristics

The biosorption of copper by the brown seaweed Sargassum baccularia,immobilized onto polyvinyl alcohol(PVA)gel beads, was investigated with fixed-bed experiments.Laboratory-scale column tests were performed to determine breakthrough curves with varying flow rates and feed concentrations.A theoretical fixed-bed model,known as the Bohart-Adams equation,was evaluated in simulating the experimental breakthrough curves.The Bohart-Adams model qualitatively predicted the breakthrough trends.PVA- immobilized seaweed biomass beads were amenable to efficient regeneration with aqueous solution containing the chelating agent ethylenediaminetetraacetic acid(EDTA).The biosorbent retained most of its original uptake capacity over three cycles of use.The excellent reusability of the biosorbent could lead to the development of a viable metal remediation technology.     

Biosorption of cadmium(Ⅱ) and lead(Ⅱ) ions from aqueous solutions onto dried activated sludge

The removal of heavy-metal ions from aqueous solutions by using dried activated sludge has been investigated in batch systems. Effect of solution pH, initial metal ion concentration, and temperature were determined. The results of the kinetic studies showed that the uptake processes of the two metal ions（Cd（Ⅱ） and Pb（Ⅱ）） followed the pseudo-second-order rate expression. The equilibrium data fitted very well to both the Langmuir and Freundlich adsorption models. The FT-IR analysis showed that the main mechanism of Cd（Ⅱ） and Pb（Ⅱ） biosorption onto dried activated sludge was their binding with amide I group.     

A novel biosorbent: characterization of the spent mushroom compost and its application for removal of heavy metals

The spent mushroom compost of Lentinus edodes was used as a biosorbent for adsorbing cadmium, lead and chromium from solutions under batch conditions for the first time. Titration of the biomass revealed that it contained at least three types of functional groups. The Fourier transform infrared spectrometry showed that the carboxyl, phosphoryl, phenolic groups were the main groups. The simulated values of pK, and molar quantity were 5.00 and 0.44 mmol/g, 7.32 and 1.38 mmol/g, 10.45 and 1.44 mmol/g, respectively. The biosorption ability increased with pH in acid condition. When 10 mg/L biomass dosage was added in, there was no significant increment of metal uptake. The maximum uptake estimated with the Langmiur isotherm model were 833.33 mg/g for Cd（ Ⅱ ）, 1000.00 mg/g for Pb（ Ⅱ ） and 44.44 mg/g for Cr（ Ⅲ ）, respectively. All the results showed that vast potential sorption capacity was existed in the biomass for adsorbing these three kinds of metals studied.     

Adsorption of Cr(Ⅲ) from acidic solutions by crop straw derived biochars

Cr（Ⅲ） adsorption by biochars generated from peanut, soybean, canola and rice straws is investigated with batch methods. Adsorption of Cr（Ⅲ） increased as pH rose from 2.5 to 5.0. Adsorption of Cr（Ⅲ） led to peak position shifts in the FFIR-PAS spectra of the biochars and made zeta potential values less negative, suggesting the formation of surface complexes between Cr^3＋ and functional groups on the biochars. The adsorption capacity of Cr（Ⅲ） followed the order： peanut straw char 〉 soybean straw char 〉 canola straw char 〉 rice straw char, which was consistent with the content of acidic functional groups on the biochars. The increase in Cr^3＋ hydrolysis as the pH rose was one of the main reasons for the increased adsorption of Cr（Ⅲ） by the biochars at higher pH values. Cr（llI） can be adsorbed by the biochars through electrostatic attraction between negative surfaces and Cr^3＋, but the relative contribution of electrostatic adsorption was less than 5%. Therefore, Cr（Ⅲ） was mainly adsorbed by the biochars through specific adsorption. The Langumir and Freundlich equations fitted the adsorption isotherms well and can therefore be used to describe the adsorption behavior of Cr（Ⅲ） by the crop straw biochars. The crop straw biochars have great adsorption capacities for Cr（Ⅲ） under acidic conditions and can be used as adsorbents to remove Cr（Ⅲ） from acidic wastewaters.     

Mechanism of Cd（II） adsorption by macrofungus Pleurotus platypus

The mechanism of Cd(II) uptake by the dead biomass of macrofungus Pleurotus platypus was investigated using di erent chemical and instrumental techniques. Sequential removal of cell wall components of the biosorbent revealed that structural polysaccharides play a predominant role in the biosorption of Cd(II). The adsorption kinetics fitted well with the pseudo second-order model suggested that the adsorption of Cd(II) on P. platypus involved a chemisorption process. Transmission electron microscopy of the cadmium exposed biomass confirmed the deposition of the metal mainly in the cell wall. Fourier transform infrared spectroscopic analysis of the metal loaded biosorbent confirmed the participation of –OH, –NH and C–O–C groups in the uptake of Cd(II). Energy dispersive X-ray analysis of the biosorbent before and after metal uptake revealed that the main mechanism of adsorption was ion-exchange. The e ectiveness of CaCl2 in the desorption of cadmium perhaps suggested the exchange of Ca2+ with Cd(II).     

Biosorption of Cu^2＋ and Zn^2＋ by raw and autoclaved Rocella phycopsis

The behavior of Cu2+ and Zn2+ biosorption onto raw and modified Roccella phycopsis from aqueous solutions was studied. Modification process was applied by autoclavation at 121°C for 30 min. The effcts of pH, initial metal concentration and biosorbent dosage were investigated. The maximum Cu2+ biosorption was achieved at pH 5.0 and the maximum biosorption capacities of 31.5 and 37.8 mg/g were recorded for raw and modified biosorbent, respectively. In the case of Zn2+ biosorption, maximum biosorption capacities were obtained at pH 4.0 as 29.1 and 35.3 mg/g for raw and modified biosorbent, respectively. Biosorption of Zn2+ and Cu2+ on all form of R. phycopsis increased much quickly with increasing initial metal concentrations from 10 to 100 mg/L. After modification process, probable changes in the surface polarity of raw and modified R. phycopsis were investigated by contact angle measurements. As expected, R. phycopsis has a polar surface and shows a highest contact angle with water, while after autoclavation water contact angle of R. phycopsis was significantly decreased from 47.5° to 34.4°.     

毛木耳(Auricularia polytricha)对水中铬的去除特性研究

以毛木耳子实体(Auricularia polytricha)为生物吸附材料,通过批量实验研究起始pH值、反应时间、生物量、Cr浓度等因素对毛木耳子实体吸附去除水中铬的影响及吸附特性。结果表明:铬的生物吸附过程明显受溶液pH影响,其中总Cr和Cr(Ⅵ)的最佳去除pH分别为2.0和1.0;48 h后生物吸附达到平衡,生物吸附剂的最佳浓度为4 g/L;A.polytricha对Cr的最大吸附容量为113.8 mg/g;在整个吸附过程中伴随着Cr(Ⅵ)转化为Cr(Ⅲ)。生物吸附剂的X射线光电能谱显示:吸附在生物吸附剂表层的Cr大都呈+3价。在等温实验中Freundlich模型能较好地模拟毛木耳子实体对Cr的等温吸附过程,同时准二级模型很好地拟合了生物吸附Cr的过程。毛木耳(A.polytricha)子实体在去除水体中的Cr方面具有很强的潜力。     

Removal of Crystal Violet from aqueous solution using powdered mycelial biomass of Ceriporia lacerata P2

A simple and efficient biosorbent prepared from powdered mycelial biomass of Ceriporia lacerata was used to removal Crystal Violet, poorly degraded as recalcitrant molecule by microorganism.     

新型生物吸附剂去除水中六价铬的研究

以Ｐｓｅｕｄｏｍｏｎａｓ ｓｐ．Ｇｘ４－１发酵培养得到的细菌胞外聚合物作吸附剂，研究其对水中重金属Ｃｒ（ＶＩ）的吸附，吸附剂对Ｃｒ（ＶＩ）吸附的最佳ｐＨ初值为０．５～２．０。Ｃｒ（ＶＩ）的吸附分三个阶段：５ｍｉｎ达７５％的快速吸附阶段；１０～４０ｍｉｎ达表现一级反应动力学吸附阶段；５０ｍｉｎ以的趋于平衡，吸附过程符合Ｆｒｅｕｎｄｌｉｃｈ和Ｌａｎｇｍｕｉｒ吸附等温方程。     

Ni2+生物吸附动力学及吸附平衡研究

研究了金属离子Ni²⁺在酿酒酵母上的生物吸附特性,内容包括生物吸附动力学和吸附等温线.生物吸附动力学结果表明,当Ni²⁺初始浓度为65.6 mg/L时,Ni²⁺在酿酒酵母上的生物吸附可以分为2个阶段,第1阶段为物理吸附,在10　min内快速达到平衡.Ni²⁺在酵母上的吸附过程可以很好地用准二级动力学方程来描述 （R²=0.999）,动力学参数k₂为0.018 4 g/(mg·min),q_e为5.96 　mg/g.吸附等温线结果表明,Ni²⁺在酿酒酵母上的生物吸附可以用Langmuir和Freundlich方程来描述,最大吸附量q_max为6.32 　mg/g.酿酒酵母可用于处理低浓度的含Ni²⁺废水.     

芽孢杆菌生物吸附处理含铜废水研究

用芽孢杆菌干菌体生物吸附去除废水中的铜离子,试验了pH、接触时间、初始铜离子浓度对该芽孢杆菌生物吸附铜的影响,结果表明:在温度为25℃、pH值5.0、初始铜离子浓度200mg/L、吸附时间不超过30min有最大吸附量16.27mg/g;此时去除率为16.27%,且25℃吸附平衡符合Langmuir等温模型与Freundlich等温模型;因此用芽孢杆菌生物吸附处理低浓度含铜废水可行、经济。     

Biosorption of cesium（Ⅰ） from aqueous solution by a novel exopolymers secreted from Pseudomonas fluorescens C-2： Equilibrium and kinetic studies

The biosorption characteristics of Cs(I) ions from aqueous solution using exopolymers (PFC02) produced from Pseudomonas fluorescens C-2 were investigated as a function of pH, biosorbent dosage, contact time and initial concentration. pH played a major role in the adsorption process, and the optimum pH for the removal of Cs(I) was 8.0. Langmuir, Freundlich and Dubinin-Radushkevich (D-R) models were applied to describe the biosorption isotherm of the Cs(I) ions by PFC02. The Lagergren first-order, pseudo second-order kinetic and intraparticle diffusion models were used to test the kinetic data. Langmuir model and D-R model fitted the equilibrium data better than the Freundlich isotherm. The monolayer adsorption capacities of PFC02 as obtained from Langmuir isotherm at 25°C was found to be 32.63 mg/g. From the D-R isotherm model, the mean free energy was calculated as 26.73 kJ/mol, indicating that the biosorption of cesium was chemisorption. The biosorption process was rapid, and the kinetic rates were best fitted to the pseudo second-order model, which indicated the biosorption process operated through chemisorption mechanism. FT-IR analysis of PFC02 showed the possible functional groups responsible for cesium adsorption were hydroxyl, carboxyl, carbonyl and sulphonate groups. SEM analysis showed the porous structure of the material while EDX analysis confirmed the adsorption of Cs(I) on PFC02. Cesium adsorbed onto the PFC02 could be desorbed efficiently using 1 mol/L HNO3, and the enrichment factor was 50.0. Furthermore, PFC02 could be reused five times with only about 8.25% regeneration loss. The developed method was successfully utilized for the removal of Cs(I) ions from aqueous solution.     

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

The potential use of Myriophyllum spicatum L. biomass as a biosorbent for the removal of copper(Ⅱ) from aqueous solution was investigated in laboratory condition. The sorption experiments were undertaken to obtain copper (Ⅱ) biosorption properties of M.spicatum L., i.e. equilibrium time, the maximum capacity, and rate constants. Copper(Ⅱ) biosorption was fast and equilibrium was attaine1 within 35 min at initial copper(Ⅱ) concentration of 6 mg/L. Different isotherm models including the Langmuir, Freundlich, Temkin and Redlich-Peterson model, were used to investigate the sorption capacity and isotherm. These models showed an excellent match with the experimental data except for the Freundlich model. According to the Langmuir coefficients, the maximum sorption capacity of copper onto M. spicatum L. was 10.80 mg/g. The kinetics of copper(Ⅱ) sorption was also analysed and rate constants were derived. It was found that the overall sorption process was best described by the pseudo second-order equation, and that intraparticle diffusion was not the rate determining step. The results of this study showed that M. spicatum L. can be considered as useful vehicles for the removal and recovery of copper(Ⅱ) from aqueous solutions.