Green-synthesized, biochar-supported nZVI from mango kernel residue for aqueous hexavalent chromium removal: Performance, mechanism and regeneration

A biochar-supported green nZVI(G-nZVI@MKB)composite was synthesized using mango kernel waste with“dual identity”as reductant and biomass of biochar.The G-nZVI@MKB with a Fe/C mass ratio of 2.0(G-nZVI@MKB2)was determined as the most favorable composite for hexavalent chromium(Cr(VI))removal.Distinct influencing parameters were discussed,and 99.0%of Cr(VI)removal occurred within 360 min under these optimized parameters.Pseudo-second order kinetic model and intra-particle diffusion model well depicted Cr(VI)removal process.The XRD,FTIR,SEM,and XPS analyses verified the key roles of G-nZVI and functional groups,as well as the primary removal mechanisms involving electrostatic attraction,reduction,and complexation.G-nZVI@MKB2 exhibited good stability and reusability with only a 16.4%decline in Cr(VI)removal after five cycles.This study offered evidence that mango kernel could be recycled as a beneficial resource to synthesize green nZVI-loaded biochar composite for efficient Cr(VI)elimination from water.

Bioremediation of Hexavalent Chromium Pollution by Sporosarcina saromensis M52 Isolated from Offshore Sediments in Xiamen, China

Objective Cr（VI） removal from industrial effluents and sediments has attracted the attention of environmental researchers. In the present study, we aimed to isolate bacteria for Cr（VI） bioremediation from sediment samples and to optimize parameters of biodegradation. Methods Strains with the ability to tolerate Cr（VI） were obtained by serial dilution and spread plate methods and characterized by morphology, 16 S r DNA identification, and phylogenetic analysis. Cr（VI） was determined using the 1,5-diphenylcarbazide method, and the optimum p H and temperature for degradation were studied using a multiple-factor mixed experimental design. Statistical analysis methods were used to analyze the results. Results Fifty-five strains were obtained, and one strain（Sporosarcina saromensis M52; patent application number： 201410819443.3） having the ability to tolerate 500 mg Cr（VI）/L was selected to optimize the degradation conditions. M52 was found be able to efficiently remove 50-200 mg Cr（VI）/L in 24 h, achieving the highest removal efficiency at p H 7.0-8.5 and 35 °C. Moreover, M52 could completely degrade 100 mg Cr（VI）/L at p H 8.0 and 35 °C in 24 h. The mechanism involved in the reduction of Cr（VI） was considered to be bioreduction rather than absorption. Conclusion The strong degradation ability of S. saromensis M52 and its advantageous functional characteristics support the potential use of this organism for bioremediation of heavy metal pollution.

Removal of hexavalent chromium in aquatic solutions by pomelo peel

This study investigated the removal of hexavalent chromium(Cr(VI)) in aqueous solutions using pomelo peel(PP) and FeCl3-modified pomelo peel(FPP) as novel biomass adsorbents.Batch adsorption experiments were performed to evaluate the effects of pH,time,temperature,initial concentration,and adsorbent dose on Cr(VI) removal by PP and FPP.The results show that the maximum adsorption capacity of Cr(VI)was 21.55 mg/g for FPP and 0.57 mg/g for PP at a pH of 2.0 and a temperature of 40℃.The surface shape,microstructure,and chemical composition of FPP were analyzed with scanning electron microscopy(SEM),Fourier transform infrared spectroscopy(FTIR),and energy dispersive spectroscopy(EDS),and compared with those of PP.The results show that the adsorption performance of FPP was much better than that of PP,indicating that FPP can be an alternative high-efficiency adsorbent for Cr(VI) removal.

Improvement of stability of trivalent chromium electroplating of Ti based IrO_2+Ta_2O_5 coating anodes

The preparation process and properties of the thermally prepared Ti anodes coated with IrO2+Ta2O5 was studied. The structure and morphologies of the IrO2+Ta2O5 coatings were determined by XRD and SEM. Their electrochemical properties were studied by polarization curve and cyclic voltammetry. Trivalent chromium electroplating using Ti/IrO2+Ta2O5 anodes is carried out and the results were analyzed. Results show that this anode exhibits excellent electrochemical activity and stability in sulfate electrolysis. The electrocatalytic activity is determined not only by the content of IrO2 but also the structure and morphology of the anode coatings. The electroplating results indicats that Ti/IrO2+Ta2O5 anodes have excellent capabilities and merits in improving the stability of trivalent chromium electroplating in sulfate system.

Application of Iron Nanoparticles Synthesized by Green Tea for the Removal of Hexavalent Chromium in Column Tests

Nano zero valent iron particles (nZVI) are popular the last few years because of the numerous applications in remediation of a wide range of pollutants in contaminated soils and aquifers. The nZVI particles can be 10 - 1000 times more reactive than granular or micro-scale ZVI particles due to the small particle size, large specific surface area and high reactivity. An alternative green synthesis procedure was used for the production of nano zero valent iron particles (nZVI) using green tea (GT) extract, which is characterized by its high antioxidant content. Polyphenols in green tea extract possess double role in the synthesis of nZVI, because they not only reduce ferric cations, but also protect nZVI from oxidation and agglomeration as capping agents. The objective of current study was to simulate ata laboratory scale the attachment of GT-nZVI particles on soil material and study the effectiveness of attached nanoparticles for removing hexavalent chromium (Cr(VI)) from contaminated groundwater flowing through the porous soil bed. Column tests were carried out with various flowrates in order to examine the effect of contact time between the attached on porous medium nZVI and the flow-through solution on Cr(VI) reduction. After the completion of column tests the soil material in each column was split in 5 vertical sections, which were further subjected to chemical analyses and leaching tests. According to the results of the study increasing the contact time favors the reduction and removal of Cr(VI) from the aqueous phase. The reductive precipitation of Cr can be described as a reaction that follows a pseudo-first order kinetic law, with rate constant equal to k = 0.0243 ± 0.0011 min-1. Leaching tests indicated that precipitated chromium is not soluble. In the examined soil material, the total amount of precipitated Cr was found to range between 280 and 890 mg/(kg soil), while soluble Cr was less than 1.4 mg/kg and most probably it was due to the presence of residual Cr(VI) solution in the porosity of soil.

Effect of polyethylene glycol on electrochemically deposited trivalent chromium layers

The structural characteristics of the trivalent chromium deposits and their interfacial behavior in the plating solution with and without polyethylene glycol molecules were observed by using various electrochemical methods such as cyclic voltammetry,open circuit potential transition,electrochemical impedance spectroscopy,scanning electron microscopy and X-ray photoelectron spectrometry.It is shown that the polyethylene glycol molecules make the reductive current density lower in the trivalent chromium plating system and promote a hydrogen evolution reaction through their adsorption on the electrode surface.And the trivalent chromium layer formed from the polyethylene glycol-containing solution has somewhat higher density of cracks on its surface and results in a lower film resistance,lower polarization resistance,and higher capacitance in a corrosive atmosphere.It is also revealed that the formation of chromium carbide layer is facilitated in the presence of polyethylene glycol,which means easier electrochemical codeposition of chromium and carbon,not single chromium deposition.

Influence of glycine additive on corrosion and wear performance of electroplated trivalent chromium coating

The aim of this study is to evaluate the effect of various molar ratios of glycine to chromium salt(Gly:Cr)and different current densities on the corrosion and wear behaviors of Cr(III)electroplated coatings.The morphology and thickness of the coatings were investigated by scanning electron microscopy.The wear properties of the coatings were studied using pin on disk and hardness tests,while corrosion behavior of the coatings was identified using linear polarization,small amplitude cyclic voltammetry,and electrochemical impedance spectroscopy methods.By increasing the glycine concentration,a structure with low crack density was obtained.In all molar ratios,maximum thickness and current efficiency was observed at a current density of 150 mA·cm?2.All the electrochemical methods had a consistent result,and maximum corrosion resistance of approximately 16000Ω·cm2 was obtained in the case of Gly:Cr=3:1 and current density of 200 mA·cm?2.

The Hardness and Corrosion Properties of Trivalent Chromium Hard Chromium

The formulation of hard chromium plating from trivalent chromium electrolyte and its related process have been intensively studied in this work. Through optimized conditions, the coating hardness can achieve more than HV0.1900 without any treatment and HV0.11700 after heat treatment for five minutes at 300°C, and the thickness of hard chromium coating was about 100 μm. The hard chromium coatings show good adhesion on the carbon steel and low alloy structural steel. The corrosion resistance of hard chromium coatings was enhanced by the adding nanometer materials into trivalent chromium plating coatings. More than 120 hours salt spray corrosion resistance can be achieved with 40 to 50 microns thickness of trivalent chromium plating coatings.

Removal of hexavalent chromium from aqueous solution by iron nanoparticles

Groundwater remediation by nanoparticles has received increasing interest in recent years. This report presents a thorough evaluation of hexavalent chromium removal in aqueous solutions using iron (Fe0) nanoparticles. Cr(VI) is a major pollutant of groundwater. Zero-valent iron, an important natural reductant of Cr(VI), is an option in the remediation of contami- nated sites, transforming Cr(VI) to essentially nontoxic Cr(III). At a dose of 0.4 g/L, 100% of Cr(VI) (20 mg/L) was degraded. The Cr(VI) removal efficiency decreased significantly with increasing initial pH. Different Fe0 type was compared in the same con- ditions. The reactivity was in the order starch-stabilized Fe0 nanoparticles>Fe0 nanoparticles>Fe0 powder>Fe0 filings. Electro- chemical analysis of the reaction process led to the conclusion that Cr(OH)3 should be the final product of Cr(VI). Iron nanopar- ticles are good choice for the remediation of heavy metals in groundwater.

Evaluation of the Adsorption of Hexavalent Chromium on Kaolinite and Illite

The adsorption of hexavalent chromium on Kaolinite and Illite was studied in order to evaluate their potential for the reduction of hexavalent chromium mobility and their possible application for the treatment of polluted sediment. The influence of various parameters affecting the adsorption of hexavalent chromium, such as the pH of aqueous solution, the ionic strength and the initial metal ion concentration were investigated. The optimal pH range corresponding to the hexavalent chromium adsorption maximum on the Kaolinite and Illite is 2 - 4 and 2 - 2.6, respectively. The results showed that hexavalent chromium sorption on Kaolinite and Illite was strongly influenced by the pH, the ionic strength and the initial metal ion concentration. Langmuir and Freundlich adsorption isotherms are employed to understand the nature of adsorption at room temperature. The characteristic parameters for each isotherm have been determined. This showed that the Freundlich isotherm model well described the equilibrium data. The data suggest that the charge of the clay mineral surface is one of the main factors controlling hexavalent chromium desorption at alkaline pHs.

Anticlastogenic Effect of Redistilled Cow's Urine Distillate in Human Peripheral Lymphocytes Challenged With Manganese Dioxide and Hexavalent Chromium

Objective To study the anticlastogenic effect of redistilled cow＇s urine distillate （RCUD） in human peripheral lymphocytes （HLC） challenged with manganese dioxide and hexavalent chromium. Methods The anticlastogenic activity of redistilled cow＇s urine distillate was studied in human polymorphonuclear leukocytes （HPNLs） and human peripheral lymphocytes in vitro challenged with manganese dioxide and hexavalent chromium as established genotoxicants and clastogens which could cause induction of DNA strand break, chromosomal aberration and micronucleus. Three different levels of RCUD： 1 μL/mL, 50 μL/mL and 100 μL/mL, were used in the study. Results Manganese dioxide and hexavalent chromium caused statistically significant DNA strand break, chromosomal aberration and micronucleus formation, which could be protected by redisfilled cow＇s urine distillate. Conclusion The redistilled cow＇s urine distillate posseses strong anfigenotoxic and antielastogenic properties against HPNLs and HLC treated with Cr^＋6 and MnO2. This property is mainly due to the antioxidants present in RCUD.

Titanium dioxide-graphene composite electrochemical sensor for detection of hexavalent chromium

Hexavalent chromium(Cr(VI))compound is useful to various industries but is toxic and carcinogenic.In this research work,we fab-ricate an amperometric sensor for the determination of Cr(VI),using a titanium dioxide(TiO2)-reduced graphene oxide(rGO)composite as the sensing element.The composite was synthesized following sol−gel chemistry,yielding TiO2 nanoparticles of~50 nm in size,immobilized on chemically exfoliated rGO sheets.The composite was employed in a 3-electrode electrochemical cell and operated in an amperometric mode,exhibiting good responses to the 50 to 500 ppb Cr(VI).Our best result from pH 3 Mcilvane’s buffer medium reveals the sensitivity of 9.12×10−4 ppb−1 and a detection limit of 6 ppb with no signal interference from 200 ppm Ca(II),150 ppm Mg(II),and 50 ppb Pb(II).The excellent results of the TiO2-rGO sensor can be attributed to synergic effects between TiO2 and rGO,resulting from the presence of n-p heterojunctions and the formation of the TiO2 nanoparticles on rGO.

Cytotoxicity and genome-wide microarray analysis of intestinal smooth muscle cells in response to hexavalent chromium induction

Chronic ingestion of high concentrations of hexavalent chromium[Cr(VI)]in drinking water induces intestinal tumors in mice;however,information on its toxicity on intestinal smooth muscle cells is limited.The present study aimed to assess the in vitro and in vivo toxicological effects of Cr(VI)on intestinal smooth muscle cells.Human intestinal smooth muscle cells(HISM cells)were cultured with different concentrations of Cr(VI)to evaluate effects on cell proliferation ability,oxidative stress levels,and antioxidant system.Furthermore,tissue sections in Cr(VI)exposed rabbits were analyzed to evaluate toxicity on intestinal muscle cells in vivo.Gene chips were utilized to assess differential gene expression profiles at the genome-wide level in 1μmol/L Cr(VI)treated cells.Intestinal tissue biopsy results showed that Cr(VI)increased the incidences of diffuse epithelial hyperplasia in intestinal jejunum but caused no obvious damage to the structure of the muscularis.Cell proliferation analysis revealed that high concentrations(≥64μmol/L)but not low concentrations of Cr(VI)(≤16μmol/L)significantly inhibited the growth of HISM cells.For oxidative stress levels,the expression of reactive oxygen species(ROS)and nitric oxide(NO)was elevated at high concentrations(≥64μmol/L)but not at low concentrations of Cr(VI)(≤16μmol/L).In addition,dose-dependent increases in the activity of oxidized glutathione(GSSH)/total-glutathione(T-GSH)were also observed.Gene chip screened 491 differentially expressed genes including genes associated with cell apoptosis,oxidations,and cytoskeletons.Some of these differentially expressed genes may be unique to smooth muscle cells in response to Cr(VI)induction.

Impact of Corrosive Liquid on Trivalent Chromium over Aluminium Alloys

Considering aviation and space sectors, aluminium alloys are commonly used due to its excellent mechanical and physical properties. Though satellite hard-ware is confined to controlled environment, it requires anticorrosive treatment over metal substrate followed by a systematic coating scheme. The trivalent chromium coating was deposited over three aluminium alloys namely AA6063, AA7075 and AA6082. The variation in corrosion resistance property of trivalent chromium over each aluminium alloy has been studied in detail. The Neutral Salt Spray (NSS) test result shows that trivalent chromium coating over AA7075 alloy is affected by pitting corrosion compared to other two alloys. In addition to that, NSS test also proves that thickness of the layer does not have any influence corrosion resistance property of trivalent chromium coating. Furthermore, ions in trivalent chromium coating was identified using Secondary Neutral Mass Spectroscopy (SNMS) and degradation of coating in a corrosive liquid studied using Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) instrument to understand mechanism of corrosion. The results indicated that both coating and substrate is involved in corrosion process. The number of elements dissolved in to salt solution reveals the weak ionic bonding of coating towards substrates. In comparison, AA7075 alloy has weaker bonding than AA6082 and AA6063 series. The alloying elements such as zinc and copper are removed from substrate by corrosive solution.

Sorption Characteristics of Hexavalent Chromium in the Soil Based on Batch Experiment and Their Implications to the Environment

The objective of this experimental study was to determine the kinetics and equilibrium sorption of Cr(VI) in soils collected from Hengshui City of Hebei Province, China, based on batch experiments. The main concentration for this paper is on the effect of soil pH, solute concentration and ionic strength as the variable factors in the sorption of Cr(VI) in soils and the assessment of their implications to the environment. Atomic Absorption Spectrophotometer (AAS) was used for Cr(III) analysis;UV-VIS Spectrophotometer for quantification of Cr(VI) in soil samples and determination of electrical conductivity and temperature of the soil samples;and Automatic Laser Particle Size Analyzer LS230 for the determination of soil physical characteristics. Results from this study show that adsorption and reduction are major reactions accounting for removal of Cr(VI) from soil solution. It is concluded that chemical reactions such as reduction, strongly influence Cr(VI) mobility in soil. Adsorption kinetics experiments indicated that Cr(VI) removal from soil solution increases with increasing solute concentration, with decreasing pH and with decreasing ionic strength. Adsorption reactions reached equilibrium within 12 hours in batch reactors. Increasing background electrolyte concentration (KCI) decreases Cr(VI) adsorption on soil. The Cr(VI) adsorption isotherm for this soils conforms well to the Langmuir isotherm at constant pH. Two Cr(VI) adsorption parameters: the maximum sorption capacity (Qo) and Langmuir adsorption constant (KL), were determined as 1.0135 × 10-4 mol/g and 0.0622 mg/L, respectively. The reduction of Cr(VI) into less toxic Cr(III), means reduction of significant environmental problems. Finally, this study advises relevant environmental governing authorities to observeperiodic monitoring of the status of Cr(VI) in soils.

Using Ferrous Ion for the Reductive Degradation of Hexavalent Chromium

This paper discusses the toxicity and mobility of chromium species. And it presents the extent and kinetics of reductive remediation of hexavalent chromium, Cr+ using ferrous ion, Fe2+. Molar ratios of 1:3 and 1:6 of Cr (VI) to Fe (II) were used. Integral method of data analysis showed reaction followed second-order kinetics with R square values near unity. Reaction was initially fast but with a rapid precipitation attributed to Cr (III)-Fe (III) in previous studies. This colloidal precipitate ultimately stops the reaction, which explains while conversion efficiency increases with increased molar ratio of Cr (VI) to Fe (II). The impact of pH was investigated by adjusting the Cr (VI)-Fe (II) medium to pH 2.78, 5.24, 7.00, 9.00 and 11.96 using predetermined drops of acid or base. Reaction was more rapid under alkaline conditions with higher extent of degradation consistent with previous research. In soil system, mass transfer limitation was hardly noticed as high extent of reduction was recorded relative to aqueous phase. The high solubility of Cr (VI) aided the release into the aqueous media for reduction by ferrous sulfate.

Non-linear modeling of kinetic and equilibrium data for the adsorption of hexavalent chromium by carbon nanomaterials:Dimension and functionalization

The adsorption capacities for the removal of hexavalent chromium from aqueous solutions by six carbon nanomaterials have been evaluated. Single-walled and multi-walled carbon nanotubes as received and after oxidation treatment, graphene oxide and reduced graphene oxide are the materials with different dimension and functionalization compared in this research. Carbon nanotubes have been modified using hydrogen peroxide as oxidizing agent under microwave radiation. The oxidation treatment on carbon nanotubes has a positive effect increasing the adsorbent–adsorbate interaction. Rate-controlling mechanisms and equilibrium data are analyzed using non-linear models. Non-linear method is proposed as the most suitable method for determining the kinetic and equilibrium parameters. The values of adsorption energy(E) obtained from the Dubinin–Radushkevich isotherm,have been found around 0.371 and 0.870 k J·mol-1, indicating physical adsorption. Therefore, the pseudo-second order model represents better the kinetic experimental data. The results show that the Langmuir isotherm provides a slightly better fit to the experimental data compared with the Freundlich isotherm, indicating homogeneous distribution of active sites on carbon nanomaterials and monolayer adsorption. The separation factors RLare found in the range of 0–1, suggesting that the adsorption process is suitable for all adsorbents. The mechanisms for hexavalent chromium removal have been proposed as electrostatic interactions and hydrogen bonding.

Study on anaerobic treatment of wastewater containing hexavalent chromium

A self-made anaerobic bio-filter bed which was inoculated with special sludge showed high efficiency in removing hexavalent chromium. When pump flow was 47 ml/min and CODCr of wastewater was about 140 mg/L, it took 4 h to decrease the Cr6+ concentrations from about 60 mg/L to under 0.5 mg/L, compared with 14 h without carbon source addition. Cr6+ concentra- tions ranged from 64.66 mg/L to 75.53 mg/L, the system efficiency was excellent. When Cr6+ concentration reached 95.47 mg/L, the treatment time was prolonged to 7.5 h. Compared with the contrast system, the system with trace metals showed clear supe- riority in that the Cr6+ removal rate increased by 21.26%. Some analyses also showed that hexavalent chromium could probably be bio-reduced to trivalent chromium, and that as a result, the chrome hydroxide sediment was formed on the surface of microor- ganisms.

Cytotoxicity and genome-wide microarray analysis of intestinal smooth muscle cells in response to hexavalent chromium induction

Chronic ingestion of high concentrations of hexavalent chromium [Cr（VI）] in drinking water induces intestinal tumors in mice; however, information on its toxicity on intestinal smooth muscle cells is limited. The present study aimed to assess the in vitro and in vivo toxicological effects of Cr（VI） on intestinal smooth muscle cells. Human intestinal smooth muscle cells （HISM cells） were cultured with different concentrations of Cr（VI） to evaluate effects on cell proliferation ability, oxidative stress levels, and antioxidant system. Furthermore, tissue sections in Cr（VI） exposed rabbits were analyzed to evaluate toxicity on intestinal muscle cells in vivo. Gene chips were utilized to assess differential gene expression profiles at the genome-wide level in 1 gmol/L Cr（VI） treated cells. Intestinal tissue biopsy results showed that Cr（VI） increased the incidences of diffuse epithelial hyperplasia in intestinal jejunum but caused no obvious damage to the structure of the muscularis. Cell proliferation analysis revealed that high concentrations （〉__64 gmol/L） but not low concentrations of Cr（VI） （〈16 ~tmol/L） significantly inhibited the growth of HISM cells. For oxidative stress levels, the expression of reactive oxygen species （ROS） and nitric oxide （NO） was elevated at high concentrations （〉64 pmol/L） but not at low concentrations of Cr（VI） （〈16 pmol/L）. In addition, dose-dependent increases in the activity of oxidized glutathione （GSSH）/total-glutathione （T-GSH） were also observed. Gene chip screened 491 differentially expressed genes including genes associated with cell apoptosis, oxidations, and cytoskeletons. Some of these differentially expressed genes may be unique to smooth muscle cells in response to Cr（VI） induction.

Flow-Injection Flame Atomic Absorption Determination of Hexavalent Chromium with On-Line Preconcentration on an Anion Imprinted Polymer

A flow injection preconcentration system for the flame atomic absorption spectrometric determination of hexavalent chromium has been developed. The method employs on-line preconcentration of Cr(VI) on a minicolumn packed with Cr(VI)-imprinted poly(4-vinyl pyridineco-2-hydroxyethyl methacrylate) placed into a flow injection system. Hexava-lent chromium was eluted with a small volume of diluted hydrochloric acid into the nebulizer-burner system of a flame atomic absorption spectrometer. An enrichment factor of 550 and a 3σ detection limit of 0.04 μg·L-1 along a sampling frequency of 4 h-1 at a sample flow rate of 3.5 mL·min-1. The relative standard deviation is 2.9% for 1 μg·L-1 Cr(VI) (n = 11). The flow injection system proposed has the advantage of being simpler because the use of expensive and sophisticated instruments is avoided. Ease of use, continuous process and selectivity make this method suitable for Cr(VI) determination in different environmental samples such as sea and river waters, soils and sediments.