Characterization of chromium-containing wastes and soils affected by the production of chromium tanning agents

Purpose

Wastes of unknown composition derived from the production of trivalent chromium (Cr(III)) salts used as tanning agents are deposited in the area of Kanpur, India. The questions of whether these samples are chromite ore processing residue (COPR) and whether Cr occurs in its toxic hexavalent form (Cr(VI)) arise.

Materials and methods

Twenty-one samples from two disposal sites and surrounding soils were analyzed, specifically examining their elemental and mineralogical composition. Additionally, aqueous eluates with different liquid-to-solid ratios were performed and analyzed for Cr(VI).

Results and discussion

The samples were classified in accordance to the sum of silicon and aluminum and the sum of calcium and Cr contents: uncontaminated, moderately contaminated, and highly contaminated material. Highly contaminated material exhibited extremely alkaline pH values up to 12.5 and total Cr contents ranging from 65.7 to 110 g/kg, whereas uncontaminated material had comparatively moderate pH values and Cr contents <1 g/kg. In total, seven crystalline phases commonly found in COPR were identified in the contaminated samples, of which five phases (brownmillerite, hydrocalumite, hydrogarnet, magnesiochromite, and periclase) are known to be able to accommodate Cr whereas hydrogarnet and hydrocalumite are the main host phases for Cr(VI). Batch tests showed that dissolution controlled the Cr(VI) concentrations in the eluates.

Conclusions

Six samples were clearly identified as highly Cr-contaminated COPR. Leaching of Cr(VI) and resulting contamination of soils and water bodies is a key environmental risk arising from these COPR sites especially during the monsoon season. This situation is of particular concern as the local population use the highly Cr(VI)-contaminated water not only for the needs of livestock and irrigation but also as drinking water due to the absence of alternative water resources.     

Chromium Speciation in Water by Sorption on Calcite and Determination by Electrothermal Atomic Absorption Spectrometry

Abstract

A rapid, sensitive, and accurate method for the separation and speciative determination of chromium (Cr)(VI) and Cr(III) in water samples has been developed using sorption as the separation technique in conjunction with final determination by electrothermal atomic absorption spectroscopy (ETAAS). The present method, where granular calcite is used as selective sorbent, separates Cr(III) with retention values up to 99%, resulting in high accuracy determination of Cr(VI). Total Cr was likewise determined by ETAAS after an efficient reduction of Cr(VI) to Cr(III) using ascorbic acid as reducing agent, deriving Cr(III) concentration from the difference between total Cr and Cr(VI). The parameters of the separation technique, solution pH (4.5–5.5), solution flow rate through the calcite column (0.14–0.42 mL min^?1), and calcite column internal diameter (1.5–3.0 cm), were evaluated. Best results were achieved with pH of 5.5, flow rate of 0.42 mL min^?1, and column internal diameter of 1.5 cm. Optimum determination conditions were found using magnesium nitrate [Mg(NO₃)₂] as chemical modifier, pyrolysis, and atomization temperatures of 1400 and 2200°C, respectively. In such conditions, the detection limits (n=10) were 1.5 and 0.8 µg L^?1 for Cr(III) and Cr(VI), respectively.     

Reduction of Hexavalent Chromium in Soil and Ground Water Using Zero-Valent Iron Under Batch and Semi-Batch Conditions

Chemical remediation of soil and groundwater containing hexavalent chromium (Cr(VI)) was carried out under batch and semi-batch conditions using different iron species: (Fe(II) (sulphate solution); Fe⁰ _G (granulated elemental iron); ZVIne (non-stabilized zerovalent iron) and ZVIcol (colloidal zerovalent iron). ZVIcol was synthesized using different experimental conditions with carboxymethyl cellulose (CMC) and ultra-sound. Chemical analysis revealed that the contaminated soil (frank clay sandy texture) presented an average Cr(VI) concentration of 456?±?35 mg kg^?1. Remediation studies carried out under batch conditions indicated that 1.00 g of ZVIcol leads to a chemical reduction of ～280 mg of Cr(VI). Considering the fractions of Cr(VI) present in soil (labile, exchangeable and insoluble), it was noted that after treatment with ZVIcol (semi-batch conditions and pH 5) only 2.5% of these species were not reduced. A comparative study using iron species was carried out in order to evaluate the reduction potentialities exhibited by ZVIcol. Results obtained under batch and semi-batch conditions indicate that application of ZVIcol for the “in situ” remediation of soil and groundwater containing Cr(VI) constitutes a promising technology.     

Activated Biochar Prepared by Pomelo Peel Using H<Subscript>3</Subscript>PO<Subscript>4</Subscript> for the Adsorption of Hexavalent Chromium: Performance and Mechanism

Adsorption of hexavalent chromium (Cr(VI)) using pomelo peel activated biochar (PPAB) as a adsorbent was investigated. The characterization of the adsorbent was studied by Brunauer-Emmett-Teller (BET), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and zeta potentials analysis. The results showed that the PPAB had a high microporous structure and the existence of organic compounds such as hemicellulose, cellulose, and lignin. Various parameters including initial Cr(VI) concentration, pH, and adsorbent dosage were studied. The results indicated that the adsorption process was pH dependent and maximum adsorption capacity of Cr(VI) was 57.637 mg/g at pH 2.0 and 35 °C with PPAB dosage of 0.05 g. The adsorption kinetics fitted well to the pseudo-second-order model and the correlation coefficients were greater than 0.999. The adsorption isotherm data could be better described with the Langmuir model, suggesting the homogeneous and monolayer adsorption. Moreover, the scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), and Fourier transform infrared spectrum (FTIR) results showed that the surface of PPAB had plenty of developed pores after activation and the modification process was deemed to proceed between the O–H groups from pomelo peel and H₃PO₄ molecules. The main adsorption mechanism was attributed electrostatic interaction and ion exchange between the surface of PPAB and Cr(VI).     

Kinetic Study of the Effect of pH on Hexavalent and Trivalent Chromium Removal from Aqueous Solution by <Emphasis Type="Italic">Cupressus lusitanica</Emphasis> Bark

Solution pH is among the most important parameters that influence heavy metal biosorption. This work presents a kinetic study of the effects of pH on chromium biosorption onto Cupressus lusitanica Mill bark from aqueous Cr(VI) or Cr(III) solutions and proposes a mechanism of adsorption. At all assayed contact times, the optimum pH for chromium biosorption from the Cr(III) solution was 5.0; in contrast, optimum pH for chromium biosorption from the Cr(VI) solution varied depending on contact time. The kinetic models that satisfactorily described the chromium biosorption processes from the Cr(III) and Cr(VI) solutions were the Elovich and pseudo second-order models, respectively. Diffuse reflectance infrared Fourier transform spectroscopy studies suggest that phenolic compounds present on C. lusitanica Mill bark play an important role in chromium biosorption from the Cr(III) solution. On the other hand, chromium biosorption from the Cr(VI) solution involved carboxyl groups produced on the bark by redox reactions between oxygen-containing groups and Cr(VI), and these were in turn responsible for the biosorption of Cr(III) produced by Cr(VI) reduction.     

Isolation and characterization of multi-potential Rhizobium strain ND2 and its plant growth-promoting activities under Cr(VI) stress

Soil contaminated by chromium (Cr) is a major concern for sustainable agriculture. Considering this as a basis, the present study was designed to isolate Cr(VI)-reducing and plant growth-promoting bacterial strain from contaminated sampling sources. In this study, Rhizobium strain ND2 was isolated from the root nodules of Phaseolus vulgaris grown in leather industrial effluent contaminated soil. The strain ND2 exhibited strong resistance to different heavy metals and reduced 30 and 50 µg ml^?1 concentrations of Cr(VI) completely after 80 and 120 h of incubation, respectively, as well as chromium adsorption and immobilization were confirmed by scanning electron microscopic equipped with energy X-ray spectroscopy. In addition, the strain produced 21.73 and 36.86 µg ml^?1 of indole-3-acetic acid at 50 and 100 µg ml^?1 of L-tryptophan supplimentations, respectively. Strain ND2 positively affected the exo-polysaccharide, ammonia, protease and catalase production and stimulated root length of various test crops under Cr(VI) stress. Moreover, Rhizobium strain ND2 has the potential to colonize the diverse agricultural crops. Thus, the present findings strongly suggested that the multipotential properties of ND2 could be exploited for bioremediation of contaminated sites with Cr(VI) as well as potential bio fertilizer for enhancing the agricultural productivity.     

Hexavalent Chromium Removal by Candida sp. in a Concentric Draft-Tube Airlift Bioreactor

The main purpose of this work was to conduct a kinetic study on cell growth and hexavalent chromium [Cr(VI)] removal by Candida sp. FGSFEP in a concentric draft-tube airlift bioreactor. The yeast was batch-cultivated in a 5.2-l airlift bioreactor containing culture medium with an initial Cr(VI) concentration of 1.5 mM. The maximum specific growth rate of Candida sp. FGSFEP in the airlift bioreactor was 0.0244 h^?1, which was 71.83% higher than that obtained in flasks. The yeast strain was capable of reducing 1.5 mM Cr(VI) completely and exhibited a high volumetric rate [1.64 mg Cr(VI) l^?1 h^?1], specific rate [0.95 mg Cr(VI) g^?1 biomass h^?1] and capacity [44.38 mg Cr(VI) g^?1 biomass] of Cr(VI) reduction in the airlift bioreactor, with values higher than those obtained in flasks. Therefore, culture of Candida sp. FGSFEP in a concentric draft-tube airlift bioreactor could be a promising technological alternative for the aerobic treatment of Cr(VI)-contaminated industrial effluents.     

Hexavalent Chromium Removal by a Trichoderma inhamatum Fungal Strain Isolated from Tannery Effluent

A fungal strain possibly capable of removing hexavalent chromium was to be isolated from industrial effluent from a leather factory located in the city of Guadalajara, state of Jalisco, Mexico. The strain was identified as Trichoderma inhamatum by the D1/D2 domain sequence of the 28S rDNA gene. Batch cultures of T. inhamatum in media containing initial Cr(VI) concentrations from 0.83 to 2.43 mM Cr(VI) were prepared. Experimental results suggest that the fungus is capable of transforming hexavalent chromium to trivalent chromium; a transformation of a highly toxic contaminant to a low toxic form. The specific and volumetric rates of Cr(VI) reduction by T. inhamatum cultures decreased as the initial Cr(VI) concentration increased. The fungus exhibited a remarkable capacity to tolerate and completely reduce Cr(VI) concentrations up to 2.43 mM. These results indicate that the T. inhamatum fungal strain may have potential applications in bioremediation of Cr(VI)-contaminated wastewaters.     

Sorption Characteristics of Chromium and Its Phytotoxic Effect with or without City Compost on Maize and Spinach in a Vertisol of Central India

Abstract

Phytotoxicity, due to chromium [Cr (VI)] additions from low to very high levels in a swell–shrink clayey soil (Haplustert), in maize and spinach was studied in a pot culture experiment. Six levels of Cr (VI) (0, 5, 10, 25, 50, and 75 mg kg^?1 soil) for maize and five levels for spinach (0, 2, 5, 10, and 25 mg kg^?1 soil) were applied singly and in combination with two doses (0 and 20 t ha^?1) of city compost. At levels of more than 75 mg Cr (VI) kg^?1 soil for maize there was virtually no growth after germination, whereas 25 mg Cr (VI) kg^?1 soil hindered the germination of spinach crop. Initial symptoms of Cr (VI) toxicity appeared as severe wilting of the tops of treated plants. Maize plants suffering from severe Cr (VI) toxicity had smaller roots and narrow brownish red leaves covered with small necrotic spots. In spinach, severe chlorosis was observed in leaves. Higher levels of Cr (VI) inhibited the growth and dry‐matter yield of the crops. However, application of city compost alleviated the toxic effect of Cr (VI). The concentration of Cr (VI) in plant parts increased when Cr (VI) was applied singly but decreased considerably when used in combination with city compost. There was evidence of an antagonistic effect of Cr (VI) on other heavy‐metal (Mn, Cu, Zn, and Fe) concentrations in plant tops. Thus, when Cr (VI) concentration increases, the concentration of other beneficial metals decreases. Chromium (VI) concentration in maize roots ranged from traces (control) to 30 mg kg^?1and were directly related to soil Cr (VI) concentration. At 25 mg Cr (VI) kg^?1 soil, yield of maize was reduced to 41% of control plants, whereas in spinach, 10 mg Cr (VI) kg^?1 soil caused a 33% yield reduction. Experimental results revealed that the maize top (cereal) is less effective in accumulating Cr (VI) than spinach (leafy vegetables). Laboratory studies were also conducted to know Cr (VI) sorption capacity of a swell–shrink clayey soil with and without city compost, and it was found that Cr (VI) sorption reaction was endothermic and spontaneous in nature.     

Feasibility Assessment of Chromium Removal from Groundwater for Drinking Purposes by Sorption on Granular Activated Carbon and Strong Base Anion Exchange

The goal of this study was to compare the performances of strong base anion (SBA) exchange and activated carbon adsorption in the removal of hexavalent chromium, Cr(VI), from a real groundwater matrix exploited for drinking purposes. Two SBA resins and three granular activated carbons (GAC) were tested by batch experiments for kinetics and equilibrium isotherm determination. SBA resins showed higher affinity toward Cr(VI) (present in raw water at about 20 μg L^?1) with respect to the GACs, with faster kinetics and higher equilibrium adsorption capacities. Among GACs, vegetal-based carbons showed higher Cr(VI) removal efficiencies than the mineral-based carbon, which can be related to the more developed textural properties. SBA resins also displayed relevant removal capacities towards nitrate and sulfate (present at mg L^?1 concentration levels), while boron (present at about 60 μg L^?1) was effectively removed by GACs. Batch experiment results were elaborated to estimate the chromium throughputs for the studied materials, to preliminary compare their performances in a real-scale application. The monitoring of a real-scale GAC adsorption stage permitted to validate throughputs estimation and confirmed that, despite being effective toward synthetic organics, GAC adsorption is a not feasible solution for Cr(VI) removal, with extremely early breakthrough. SBA exchange process resulted to be the most suitable solution, providing the best sorbent usage rates. However, SBA resin usage rates can strongly increase when considering the removal of nitrate and sulfate ions, requiring much shorter cycle times.     

Behaviour of Reduction–Sorption of Chromium (Vi) from an Aqueous Solution on a Modified Sorbent from Rice Husk

A carbonaceous sorbent produced from rice husk via sulphuric acid treatment was used to remove Cr(VI) from aqueous solutions varying contact time, pH, Cr(VI) concentration and sorbent status (wet and dry). Cr(VI) was removed from the aqueous solution via reduction to Cr(III) and sorption. Reduction and sorption processes were investigated in terms of kinetics and equilibrium. The rate of reduction removal of Cr(VI) at pH 2 followed a pseudo first-order model while the rate of sorption of total chromium followed pseudo second-order model. Chromium sorption was highly dependent on the initial pH value with reduction taking place in solution with pH up to 7 showing sorption maxima in the pH range 1.8–2.8 for concentration range 100–500 mg/l with an increase in the equilibrium pH. Carbon dioxide evolved from the sorption media was determined. Reduction–sorption mechanism was investigated via physicochemical tests including cation exchange capacity, base neutralization and sorbent acidity in addition to FTIR studies for sorbent samples before and after sorption reaction.     

Experimental Study on Adsorption of Hexavalent Chromium with Microwave-Assisted Alkali Modified Fly Ash

Coal fly ash, a kind of solid waste generated from coal-fired power stations, can be used as an absorbent for Cr(VI) from aqueous solution. The adsorption characteristics of microwave-assisted alkali modified fly ash to hexavalent chromium had been investigated. Many experimental conditions including pH, contact time, temperature, and fly ash dosage have significant impacts on adsorption performance of modified fly ash. The optimum conditions for the preparation of modified fly ash were as follows: microwave power 600 W, microwave temperature 60 °C, and microwave time 10 min. Batch experiments on adsorption isothermal characteristics of the fly ash modified under the optimal conditions were carried out. The results show that the adsorption of hexavalent chromium ions by modified fly ash is in accordance with the Freundlich and Langmuir isotherm adsorption models, which indicates that the adsorption process is monomolecular adsorption. Environmental-benign utilization of fly ash as low-cost adsorbents in wastewater treatment would bring long-term economic and environmental benefits.     

Microbial Sulfate Reduction and Biogeochemistry of Arsenic and Chromium Oxyanions in Anaerobic Bioreactors

A pilot-scale anaerobic bioreactor with high levels of microbial sulfate reduction, known to be capable of removing cationic metals from a metal- and acid-contaminated waste stream, was utilized to determine if the system would be effective in removing metals in the form of oxyanions such as arsenate and chromate. The system removed 90 % to >99 % of the arsenic and between 86 % and 94 % of the chromium from a waste stream containing 5 mg/L of each. Cadmium, copper, iron, lead, and zinc also were removed. An equilibrium geochemistry computer modeling code, MINTEQAK, modified from MINTEQA2, was used for the chemical modeling of processes in the bioreactor. Experimental evidence on the chemical and biological reduction of arsenic and chromium and fluorescent diffraction analysis of precipitates support the following hypotheses: the primary removal process for chromium was the reduction of Cr(VI) to Cr(III) by sulfides, followed by precipitation of chromium hydroxide [Cr(OH)_3(s)]; removal of arsenic was by direct microbial enzymatic reduction of As(V) to As(III) followed by precipitation of arsenic sulfides (As₂S₃ or AsS). Experimental evidence and modeling with MINTEQAK confirmed that 90 % to 95 % of the removal of arsenic and chromium occurred in the first quarter volume of the bioreactor. Additional removal of arsenic and chromium occurred in the remaining volume of the bioreactor. The use of a sulfate reduction-based anaerobic treatment system was effective for metal-laden wastewater with elevated concentrations of arsenic and chromium.     

Tracking of Chromium in Plasma co-Melting of Fly Ashes and Sludges

Leachable chromium in the incineration fly ash and wastewater sludge has been thermally stabilized by plasma melting at the temperature of 1,773?K. To better understand how chromium is stabilized with the high-temperature treatment, chemical structure of the slags sampled at temperature zones of 1,100?C1,700?K has been studied by synchrotron X-ray absorption spectroscopy. The component-fitted X-ray absorption near edge structure spectra of chromium indicate that the main chromium compounds in the sludge and fly ash are Cr(OH)₃, Cr₂O₃, and CrCl₃. A small amount of toxic CrO₃ is also observed in the fly ash. In the plasma melting chamber under the reducing environment, the high-oxidation state chromium is not found. The slags in the plasma melting chamber have much less leachable chromium, which is due to chemical interactions between chromium and SiO₂ in the slags. The existence of the interconnected Cr-O-Si species is observed by refined extended X-ray absorption fine structure spectroscopy. In the Cr₂O₃ phase of the slags, their bond distances, and coordination numbers for the first (Cr-O) and second (Cr-(O)-Cr) shells have insignificant perturbation when experienced with different melting temperatures between 1,300 and 1,700?K. It seems that Cr₂O₃ and chromium encapsulated in the silicate matrix of the slags have relatively much lower leachability. With this concept, to obtain a low chromium leachability slag from the plasma melting process, the residence time of the melting chamber may be decreased, and the slag discharge temperatures may be increased to 1,300?K. This work also exemplifies utilization of molecule-scale data obtained from synchrotron X-ray absorption spectroscopy to reveal how chromium is thermally stabilized in a commercial scale plasma melting process.     

Treatment of Cr(VI)-spiked soils using sulfur-based amendments

The objective of this research was to assess the hexavalent chromium (Cr(VI)) reducing efficiency of sulfur-based inorganic agents including calcium polysulfide (CPS), iron sulfide (FeS), pyrite (FeS₂) and sodium sulfide (Na₂S) in three soils. An alkaline soil (soil 1), a neutral soil (soil 2) and a slightly acid soil (soil 3) constituted the investigated soils. The soils were spiked with two levels of Cr(VI) (100 and 500 mg Cr(VI) kg^?1 soil) and incubated at field capacity (FC) for one month. Then, CPS, FeS, FeS₂ and Na₂S were added at 0, 5 and 10 g kg^?1 and the concentrations of exchangeable Cr(VI) were measured after 0.5, 4, 48 and 168 h in a batch experiment. The pH and organic carbon content of the soils played predominant role in Cr(VI) self-reduction by the soil itself. Complete self-reduction of Cr(VI) from soils 1, 2 and 3 was achieved at maximum Cr(VI) levels of 1, 50 and 500 mg kg^?1, respectively. Therefore, the concentration of Cr(VI) should not exceed the given levels in order to ensure that Cr(VI) is not released into the environment from contaminated sites. Moreover, decreasing pH in the alkaline soil caused significant increase of Cr(VI) reducing efficiency. Na₂S, CPS and FeS, in contrast to FeS₂, were efficient Cr(VI) reducing agents in all three soils. For all added amendments the following order of Cr(VI) reducing capacity was observed: Na₂S > CPS > FeS > FeS₂ in soil 1, Na₂S ? CPS ~ FeS > FeS₂ in soil 2 and Na₂S ? FeS > CPS ~ FeS₂ in soil 3.     

Characterization of Reactive Red-120 Decolorizing Bacterial Strain Acinetobacter junii FA10 Capable of Simultaneous Removal of Azo Dyes and Hexavalent Chromium

Continual discharge of textile wastewaters loaded with a variety of synthetic dyes and metals is considered as a huge threat to surrounding ecosystems. In order to treat these undesirable pollutants, microbial bioremediation is considered as an efficient and economical technique. This study was conducted to evaluate the use of bacterial strains for simultaneous removal of azo dyes and hexavalent chromium [Cr(VI)]. Fifty-eight bacterial strains were isolated from Paharang drain wastewater and tested for their potential to decolorize reactive red-120 (RR-120) in the presence of 25 mg L^?1 of Cr(VI). Among the tested isolates, FA10 decolorized the RR-120 most efficiently and was identified as Acinetobacter junii strain FA10. Based on quadratic polynomial equation and response surfaces given by the response surface methodology (RSM), Cr concentration and pH were found to be the main factors governing the RR-120 decolorization by FA10. The strain FA10 also exhibited a substantial salt resistance since it showed a considerable decolorization of RR-120 even in the presence of 150 g L^?1 of NaCl. Moreover, the strain FA10 also showed the potential to simultaneously remove the Cr(VI) and the selected azo dyes in the same medium. More than 80 % of the initially added Cr(VI) was removed over 72 h of incubation along with the appreciable decolorization efficiency. The strain FA10 also exhibited good tolerance to considerable levels of different heavy metals. The findings of this study suggest that the strain FA10 might serve as an efficient bioresource to develop the biotechnological approaches for simultaneous removal of different azo dyes and heavy metals including Cr(VI).     

Chromium speciation in natural waters draining contaminated land,Glasgow, U.K.

Historically, solid waste from chromite ore processing has been disposed of at a number of sites in Glasgow, Scotland. Leachate from these sites has been implicated as a source of chromium (Cr) contamination to both groundwaters and stream waters in the south east area of the city. In this study, chromium speciation has been determined in ground-, stream-, river- and pore waters, to assess the extent of contamination and the associated risk. The speciation of chromium is important, as the trivalent species of chromium (Cr(III)) is an essential form of the element, while hexavalent chromium (Cr(VI)) is a known carcinogen to humans via inhalation. Concentrations of total chromium have also been determined in sediments from the River Clyde, to assess the significance of local concentrations relative to those elsewhere in the catchment. High concentrations of Cr(VI) were found in groundwaters and streamwaters in the area immediately surrounding the contaminated sites, and high concentrations of chromium were also found in River Clyde sediments downstream of these sites. However, these concentrations rapidly decrease away from the chromium-contaminated south eastern side of the city. Data from porewaters suggest that some reduction of Cr(VI) occurs naturally in the sediments, indicating that the risk posed by high concentrations of Cr(VI) should be decreased over the longer term.     

动态条件下壳聚糖稳定纳米铁去除水体中Cr（Ⅵ）的研究

以重金属Cr（Ⅵ）为目标污染物,在两种实验条件下（实验柱Ⅰ为模拟污染水样,实验柱Ⅱ为实际污染水样）考察了壳聚糖稳定纳米铁对Cr（Ⅵ）的去除能力。实验柱Ⅰ和实验柱Ⅱ分别在第160PV和127PV时发生了击穿效应。与实验柱Ⅰ相比,实验柱Ⅱ中壳聚糖稳定纳米铁对Cr（VI）的去除能力降低了25％。SEM表征显示,实验柱Ⅱ中壳聚糖稳定纳米铁的表面形成了许多葡萄状晶体,它们的存在导致实验柱Ⅱ中纳米铁的去除能力明显低于实验柱Ⅰ。XPS表征显示,由于Ca和Mg的氢氧化物替代了部分铁氢氧化物,导致实验柱Ⅱ中壳聚糖稳定纳米铁表面Fe原子的相对含量低于实验柱Ⅰ。Cr元素高分辨率XPS能谱分析显示,在实验柱Ⅰ的条件下CKVI）被还原得更充分,而且在两种实验条件下都有部分Cr（VI）被吸附在纳米铁表面最终没有被零价铁所还原。     

Influence of Chromium with Vermicompost on Growth and Accumulation by Brahmi

Abstract

A pot experiment was conducted under glasshouse conditions during 2004 on brahmi (Bacopa monnieri) at the Central Institute of Medicinal and Aromatic Plants (CIMAP) in Lucknow. The study was conducted to evaluate the influence of different levels of chromium (Cr), with and without vermicompost, on growth and yield, as well as on accumulation of Cr by Bacopa. Rooted cuttings of Bacopa were grown under three levels of Cr (10, 20, and 40 ppm), two levels of vermicompost (2.5 and 5 g kg^?1 soil), and a combination of both. The results indicated that herb yield increased with the joint application of vermicompost and chromium, as compared to compost and Cr alone. Application of Cr only decreased nitrogen (N) and increased phosphorus (P) concentration in plants with increase in its supply, whereas application with vermicompost raised N concentration. Chromium concentration in plant tissue was found to be highest at supply of Cr at 40 ppm+vermicompost 5 g kg^?1 soil. Increase in the supply of Cr only (10, 20, and 40 ppm) decreased iron (Fe), copper (Cu), and zinc (Zn) concentration in plants. The experiment suggests that brahmi, because of its high accumulation ability, could be used as a scavenger to clean Cr‐contaminated soil.     

Comparison of Several Amendments for In-Site Remediating Chromium-Contaminated Farmland Soil

Hexavalent chromium (Cr(VI)), which has been classified as a Group A human carcinogens list by the United States Environmental Protection Agency, possesses stronger biological toxicity, and its discharge into farmland has become a pressing environmental problems. To screen the cost-efficient Cr(VI)-contaminated soil in situ amended materials, the effects of ordinary zero-valent iron (ZVI), nanoscale zero-valent iron (nZVI), biochar (B), biochar/zero-valent iron (BZVI), and biochar/nanoscale zero-valent iron (BnZVI) on the immobilization of Cr(VI) in spiked soil (Cr(VI) = 325 mg kg^?1, Cr_total = 640 mg kg^?1) were compared in this paper. After 15 days remediation by those materials, toxicity characteristic leaching procedure and physiological-based extraction test showed that the Cr(VI) leachability and bioaccessibility were reduced by 14–92% and 4.3–92% respectively, and the order of immobilization was found to be nZVI > BnZVI > BZVI > ZVI > B. Moreover, sequential extraction procedure indicated that all materials can increase the proportion of the residual Cr, and nZVI had the most significant effect. Plant seedling growth test proved that the nanoscale zero-valent iron was able to reduce the toxicity of chromium in plants greatly in a short time, while BnZVI treatment is more favorable to the growth of plants. To sum up, the nano zero-valent iron and biochar combined treatment not only removed Cr(VI) and immobilized total chromium efficiently but also enabled plant growth in relative high chromium-containing soil.