Biosorption mechanism of Cr (Ⅵ) onto cells of Synechococcus sp.

The biosorption mechanism of Cr (Ⅵ) ions on Synechococcus sp. biosorbent was studied by analyzing the biosorption kinetics as well as speciation change and bond formation during the biosorption process. The kinetics study shows that the adsorption process of Cr (Ⅵ) consists of a very fast stage in the first several minutes, in which more than half of the saturation adsorption is attained, and a slower stage that approximately follows the first order kinetic model, basically Freundlich isotherm models were observed. Comparative studies of FT-IR spectra of K_2Cr_2O_7, free cells of Synechococcus sp., and Cr-bound cells of Synechococcus sp. show that the speciation of chromium that binds to the cells of Synechococcus sp. is Cr (Ⅲ), instead of Cr (Ⅵ), and the carboxylic, alcoholic, amido and amino groups may be involved in the binding of Cr (Ⅲ). Integrative analyses of the surface electric potential, the effect of pH value on adsorption behavior of Cr (Ⅵ), and the results of FT-IR show that the biosorption of Cr (Ⅵ) follows two subsequent steps, biosorption of Cr_2O_(7~)2-))by electrostatical force at the protonated active sites and reduction of Cr_2O_(7~(2-)) to Cr3+ by the reductive groups on the surface of the biosorbents.     

Rapid biosorption and reduction removal of Cr（Ⅵ） from aqueous solution by dried seaweeds

Four types of common seaweeds（Laminaria japonica,Undaria pinnatifida,Porphyra haitanensis,and Gracilaria lemaneiformis） were examined to remove Cr（Ⅵ） ions from aqueous solution.The experimental parameters that affected the biosorption process including pH,biomass dosage,contact time and temperature were investigated via batch experiments.The surface characteristics of seaweeds before and after Cr（Ⅵ） adsorption were studied with scanning electron microscopy and Fourier transform infrared spectroscopy.The results show that an initial solution with the pH of 1.0 is most favorable for Cr（Ⅵ） adsorption.Rapid adsorption is observed in the initial stage and adsorption equilibrium state is reached within 1 h.The adsorption efficiency by Porphyra haitanensis is the maximum among four types of seaweed powders,followed by Laminaria japonica and Undaria pinnatifida with biosorption efficiency up to 90%.The removal rate of Gracilaria lemaneiformis is less than 60%.The kinetic data obtained using the seaweeds are found to follow pseudo-second order kinetic model.Experimental sorption data adequately correlate with the Langmuir model.FTIR indicates that amino and carboxyl groups play an important role in the process of Cr（Ⅵ） adsorption and a large percentage of Cr（Ⅵ） ions are reduced by reductive groups on the surface of seaweeds.     

Removal of anionic ions from single material solution by bauxite tailings modified with FeCl3·6H2O

The adsorbabilities of the unmodified and modified bauxite tailings for Cr（Ⅵ）, As（Ⅴ） and F（Ⅰ） ions were investigated. Batch experiments were carried out to determine the removal rate as a function of adsorbent dosage, solution pH value and shaking time. The results show that the maximum removal rates of Cr（Ⅵ）, As（Ⅴ） and F（Ⅰ ） are respectively 99%, 99% and 90% by using the modified bauxite tailings. The isoelectric point of the unmodified bauxite tailings is 3.6, and that of the modified bauxite tailings is 5.0, which shifts to lower pH values in Cr（Ⅵ） solution. This indicates a specific adsorption of the anionic species on the modified bauxite railings. A new band of Cr2O72 appears in the FTIR, showing that Cr（Ⅵ） is adsorbed on the modified bauxite railings in the form of chemistry adsorption. The adsorption data of Cr（Ⅵ） on the modified bauxite tailings are well described by Freundlich model. The investigations of kinetic models show that pseudo-second-order kinetic model provides the best correlation for the experimental data.     

Chemieal Strueturcs and Adsorptive Behaviors of Superplastieizers on β-C2S

The chemical structures of four types of superplasticizers （SPs） and their adsorptive behaviors on β-C2S were investigated. The adsorption properties of SPs on β-C2S were measured and the relationship between the adsorption quantity and the specific surface of β-C2S was analyzed. The experimental results show that the adsorption quantity increases with the surface area increase of β-C2S, but the adsorption quantity per surface area is similar, which means that the main adsorbent is β-C2S itself. Polycarboxylic ester （PCE） showed the highest adsorption amount on β-C2S, followed by β-naphthalene sulfonates （NSF） and formaldehyde-acetone condensates sulfonates （FAS）, amino sulphonate （AS） showed the least adsorption amount on β-C2S. PCE affected the surface potential of β-C2S particles in water differently in comparison with other types of SPs. The adsorption capacity of SPs on β-C2S is determined by factors such as molecular structure, functional groups and molecular weight of SPs.     

Adsorption of copper（ Ⅱ ） and chromium（Ⅵ） on diaspore

The adsorption of Cu（ Ⅱ ） and Cr（Ⅵ） on diaspore was studied with the help of X-ray diffraction analysis, BET measurement, zeta potential measurement and atomic adsorption spectrometry. The adsorption equilibrium almost reaches within 60 min. The adsorption isotherms of Cu（ Ⅱ ） and Cr（Ⅵ） could be well described by the Langmuir equation. The adsorption capacities of Cu（Ⅱ） and Cr（Ⅵ） are 1.944 and 1.292 mg/g, respectively. The adsorption percentage of Cr（Ⅱ ） increases with the increment of solution pH, but the adsorption percentage of Cr（Ⅵ） decreases. This could be explained by zeta potential theoretical and electrostatic attraction between metal ions and diaspore surface.     

Single-step synthesis of magnetic chitosan composites and application for chromate(Cr(Ⅵ)) removal

Magnetic chitosan composites(Fe3O4@chitosan) were synthesized in one single-step, characterized and applied in Cr(VI) removal from water. With the increase of loading proportion of chitosan, Cr(Ⅵ) adsorption capacity of Fe3O4@chitosan composites increased from 10.771 to 21.040 mg/g. The optimum adsorption capacities of Cr(VI) on Fe3O4@chitosan-3 were found in a pH range of 3.0-5.0. Kinetic study results show that the adsorption process follows pseudo-second-order model, indicating that the rate-limiting step in the adsorption of Cr(Ⅵ) involves chemisorptions. Moreover, FT-IR spectra analysis confirms that the amine and hydroxyl groups of chitosan are predominantly responsible for binding. Results from this work demonstrate that the prepared Fe3O4@chitosan composites possess great potential in Cr(Ⅵ) removal from contaminated water.     

Thermodynamics and density functional theory study of potassium dichromate interaction with galena

The adsorption heat and reaction rate constant of potassium dichromate on the surface of galena were studied. The results indicate that potassium dichromate tends to adsorption on the galena surface. The reaction order is only 0.08385, suggesting that the concentration of potassium dichromate has little influence on its adsorption on the galena surface. In addition, the simulation of CrO2 4- adsorption on the PbS （100） surface in the absence and presence of O2 was carried out by density functional theory （DFT）. The calculated results show that CrO2 4- species adsorb energetically at the Pb-S bond site, and the presence of O2 can enhance this adsorption.     

Adsorbability of Mycobacterium phlei on hematite surface

The adsorption of microorganisms on the mineral surface is the base of microorganisms that are considered as mineral processing reagents. The principles of the use of a highly hydrophobic and negatively charged bacterium, Mycobacterium phlei, as a flocculating-flotating agent for finely divided hematite were investigated. The flocculating-floating recovery is strongly dependent on the pH and the dosage of the bacterium. Generally the pH should be controlled over the range of 5.5-7, and the dosage should be controlled about 16 mg/L. The infrared spectrometry analysis indicates that the six functional groups of M. phlei, substituted aromatic compound groups, -（CH2） n-groups, -CH2（-CH3） groups, carbonyl groups, aromatic hydrocarbon groups, and carboxyl groups, are on the hematite surface, among which the first five ones contribute physical adsorption and only the carboxyl groups provide chemisorption. Microscopic analysis reveals that the dimensions and tight aggregation degree of the flocs of hematite particles formed by M. phlei are also impacted by the pH and the content of M. phlei in flotation.     

Removal of anionic ions from single material solution by bauxite tailings modified with FeCl3·6H2O

The adsorbabilities of the unmodified and modified bauxite tailings for Cr(Ⅵ), As(Ⅴ) and F(Ⅰ) ions were investigated. Batch experiments were carried out to determine the removal rate as a function of adsorbent dosage, solution pH value and shaking time. The results show that the maximum removal rates of Cr(Ⅵ), As(Ⅴ) and F(Ⅰ) are respectively 99%, 99% and 90% by using the modified bauxite tailings. The isoelectric point of the unmodified bauxite railings is 3.6, and that of the modified bauxite tailings is 5.0, which shifts to lower pH values in Cr(Ⅵ) solution. This indicates a specific adsorption of the anionic species on the modified bauxite tailings. A new band of Cr2O72- appears in the FTIR, showing that Cr(Ⅵ) is adsorbed on the modified bauxite tailings in the form of chemistry adsorption. The adsorption data of Cr(Ⅵ) on the modified bauxite tailings are well described by Freundlich model. The investigations of kinetic models show that pseudo-second-order kinetic model provides the best correlation for the experimental data.     

Adsorption behavior of heavy metal ions by carbon nanotubes grown on microsized Al2O3 particles

Carbon nanotubes （CNTs） were grown on the surface of microsized Al2O3 particles in CH4 atmosphere at 700℃ under the catalysis of Fe-Ni nanoparticles. The CNTs on Al2O3 were used for adsorbing Pb^2＋, Cu^2＋, and Cd^2＋ from the solution and the results were compared with active carbon powders, commercial carbon nanotubes, and Al2O3 particles. The as-grown CNTs/Al2O3 have demonstrated extraordinary absorption capacity with further treatment or oxidation, as well as hydrophilic ability that other CNTs lacked. The adsorption capacity of CNTs on Al2O3 is superior to other adsorbents and the preference order of adsorption on composite Al2O3 is pb^2＋〉Cu^2＋〉Cd^2＋. It seemed that the adsorption of those Pb^2＋, Cu^2＋, and Cd^2＋ did not change the surface properties of composite particles. The adsorption behaviors of Pb^2＋, Cu^2＋, and Cd^2＋ by CNTs on Al2O3 match well with the Langmuir isothermal adsorption model and the second order kinetic model. The calculated saturation amount adsorbed by 1 g of CNTs on Al2O3 are 67.11, 26.59, and 8.89 mg/g for Pb^2＋, Cu^2＋, and Cd^2＋ in single adsorption test, respectively.     

Removal of lead in wastewater by immobilized inactivated cells of Rhizopus oligosporus

A novel technology for lead removal with nonliving Rhizopus oligosporus immobilized in calcium alginate was studied. The results show that the main influencing factors include pH value and interfering cations. pH value has different effects on biosorption of various heavy metals and lead adsorption can be proceeded by controlling pH value in a range of 2-5; interfering cations especially Cu( Ⅱ ) can make the adsorption amount of Pb( Ⅱ ) decrease by immobilized Rhizopus oligosporus. Desorption efficiency of different eluants and kinetics were investigated. Citrate the reaction equilibrium reaches 3 h. Immobilized biomass keeps high lead biosorption capacity after five cycles of regeneration.     

Adsorption and desorption properties of D318 resin for Cr（Ⅵ）

The adsorption capability of D318 resin for Cr(VI) was investigated by chemistry analysis. Experimental results show that D318 resin has the best adsorption ability for Cr(VI) at pH=3.16 in HAc-NaAc medium. The statically saturated adsorption capacity of the resin is 265.4 mg/g. The thermodynamic adsorption parameters, enthalpy change ΔH and free energy change ΔG ₂₉₈ of the adsorption reaction are 4.81 and −5.16 kJ/mol, respectively. The apparent activation energy E _a is 22.4 kJ/mol. The adsorption behavior obeys the Freundlich isotherm. The molar coordination ratio of the functional group of resin to Cr(VI) is 3:2. Cr(VI) adsorbed on D318 resin can be eluted by 5%NaOH-5%NaCl quantitatively. Foundation item: Project (Y304121) supported by the Natural Science Foundation of Zhejiang Province, China     

Removal of Cr (VI) from aqueous solution using ultrafine coal fly ash

Coal fly ashes WSRA and BQRA were ball milled for 5 h to produce their ultrafine coal fly ashes WSUA and BQUA, respectively. Batch kinetic, isotherm and pH effect on adsorption were studied to evaluate removal of Cr (VI) from aqueous solutions by ultrafine coal fly ashes comparing with raw coal fly ashes. The kinetics of adsorption indicates the process to be intraparticle diffusion controlled and follows the Lagergren first-order kinetics for all coal fly ashes. The first-order rate constants (k ₁) of Cr (VI) adsorption onto WSRA, WSUA, BQRA and BQUA are 1.981, 1.497, 2.119 and 1.500 (×10⁻²) min⁻¹, respectively. The adsorption capacities of WSUA and BQUA are much better than those of WSRA and BQRA. Equilibrium adsorption data of all coal fly ashes well satisfy the Langmuir isotherm. The adsorbed amounts of Cr (VI) onto WSUA and BQUA decrease from pH 2 to pH 6 and then increase up to pH 12.     

Speciation of chromium in soil inoculated with Cr（Ⅵ）-reducing strain, Bacillus sp. XW-4

Cr(VI)-amended soil was inoculated with Cr(VI)-reducing strain, Bacillus sp. XW-4 and incubated at 28 °C in an incubator. Cr(VI) reduction, available Cr and Cr fraction in soils were studied. The results show that addition of Bacillus sp. XW-4 can promote Cr(VI) reduction, but inoculation of this strain has a negative effect on the decrease of available Cr content in soil. In controls (without this strain) amended with 100 and 200 mg/kg of Cr(VI), Cr(VI) contents decrease to about 41 and 92 mg/kg respectively after incubation of 4 d, while in soil inoculated with XW-4, Cr(VI) contents decrease to about 18 and 60 mg/kg, respectively. The content of available Cr in soils with inoculation of XW-4 is higher than that in controls. Chromium is partitioned into water soluble Cr, exchangeable Cr, precipitated Cr, Cr bound to organics and residual Cr. The highest content of Cr is observed in residual form and water soluble Cr is not detected for all treatments after 42 d, but the soils inoculated with Bacillus sp. XW-4 contain higher content of exchangeable Cr and lower content of precipitated Cr than the soil without the inoculum. Inoculation of Bacillus sp. XW-4 can increase chromium activity in soils. Foundation item: Project(20050532009) supported by the Doctoral Foundation of Ministry of Education of China; Project supported by Program for Changjiang Scholars and Innovative Research Team in University     

Single crystal β-Ga2O3: Cr grown by floating zone technique and its optical properties

β-Ga2O3 Cr single crystals were grown by floating zone technique. Absorption spectra and fluorescence spectra were measured at room temperature. The values of field splitting parameter Dq and Racah parameter B were obtained by the peak values of absorption spectra. The value 10Dq/B=23.14 manifests that in -Ga2O3 crystals Cr3 ions are influenced by low energy crystal field. After high temperature annealing in air, the Cr3 intrinsic emission was enhanced and the green luminescence disappeared. The strong and broad 691 nm emission was obtained at 420 nm excitation due to the electron transition occurred from 4T2 to 4A2. The studies manifest that the β-Ga2O3 crystals have the potential application for tunable laser.     

Influence of Yttrium Ion-implantation on Oxidation Kinetics of Co-40Cr Alloy and Property of Oxide/Substrate Interface

The isothermal and cyclic oxidizing kinetics of Co-40Cr alloy and its yttrium ion-implanted samples were studied at 1000℃ in air by thermal-gravity analysis （TGA）. Scanning electronic microscopy （SEM） was used to examine the Cr203 oxide film＇s morphology after oxidation. Secondary ion mass spectroscopy （SIMS） method was used to examine the binding energy change of chromium caused by yttrium doping. Acoustic emission （AE） method was used in situ to monitor the cracking and spalling of oxide films formed on both samples during oxidizing and subsequent air-cooling stages. It is found that yttrium implantation remarkably reduces the isothermal oxidizing rate of Co-40Cr and improves the anti-cracking and anti-spalling properties of Cr2O3 oxide film. The reasons for the improvements are mainly that implanted yttrium reduces the grain size of Cr2O3 oxide, increases the high temperature plasticity of oxide film, and remarkably reduces the number and size of Cr2O3/Co-40Cr interfacial defects.     

Selective leaching of chromium-containing slag by HCl

A batch of column experiments was carried out to investigate the change of Cr（Ⅵ） concentration leached out from chromium-containing slag with HCI as leaching agent, and to study influences of pH, ratio of solid mass to solution volume, flow velocity and temperature on Cr（Ⅵ） leaching. The optimal parameters were obtained for Cr（Ⅵ） leaching and a fitting model was established to describe the procedure of Cr（Ⅵ） leaching. The results show that Cr（Ⅵ） concentration in leachate increases with decreasing pH and increasing flow velocity and temperature. Moreover, Cr（Ⅵ） leaching percentage increases with increasing ratio of solid mass to solution volume. The optimal parameters for Cr（Ⅵ） selective leaching are as follows： pH=3.0, 1：5 of ratio of solid mass to solution volume, 180 mL/min of flow velocity and 40 ℃ of temperature. The procedure of Cr（Ⅵ） leaching fits well with the model： v= 1.87t^-0.54, indicating that the leaching rate of Cr（Ⅵ） declines in an exponential order of-0.54.     

Electrical Transport and Magnetic Properties of La0.67Ca0.33Mn1-xCrxO3 and La0.67＋xCa0.33-x Mn1-xCrxO3 （0.04≤x≤0.08）

A comparative study for two different series, La0.67Ca0.33Mn1-xCrxO3 and La0.67＋xCa0.33-x Mn1-xCrxO3 is performed with x changing from 0.04 to 0.08 through measurements of zero-field resistivity （p）, magnetoresistance （MR） and ac susceptibility （Z） as functions of temperature （T）. For the second group, a single insulator-metal transition was characterized by the resistivity maximum appears in p vs. T curve. For the first group, besides the resistivity peak appearing at higher temperatures, the sample shows evidence for the existence of another peak appearing at lower temperatures. Compared to the first group, the second group shows a significant enhancement in MR effect, while the measurement ofΧ-T dependence does not display obvious differences for the two series. Different behaviors observed in the two series are discussed by considering possible exchange interaction between Mn^3- ion and Cr^3- ion.     

Microscopic phase-field simulation of Cr atom substitution character during formation of Ll2 and DO22 phases in Ni-Cr-Al alloy

The simulations of Cr atom substitution character during the formation of L12 and DO22 phases in Ni-Cr-Al alloy were performed at 873 K based on microscopic phase-field model. It is found that the substitution of Cr is affected by Cr and Al contents and limits of occupation probabilities of Cr atom in L12 phase are present. The precipitate is single L12 phase when the component is less than the limit, Cr atoms substitute the Al sublattices in Ll2 phase, and both of atoms Al and Cr occupy the β-sites and complex phases Ni3（Al1-xCrx） are formed; Cr atoms enter Ni sites when Al and Cr contents exceed the limit, and substitute β-sites or both of α- and β-sites. The DO22 phase is formed at the boundary of Ll2 phase.