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1.
The removal of hexavalent chromium from wastewater streams has received an considerable attention in recent years, since it can cause harmful effects on the environment. Several approaches, including adsorption, are recognized to tackle this problem, but unfortunately most of these processes are impressed with practical conditions of the experiments. The main objective of this study was to recognize applicable conditions for Cr(VI) removal from an industrial drainage using nature-derived adsorbents (brown coal and modified zeolite) and to make the process more adaptive by using adsorbents conjointly. Batch experiments were carried out by agitating Cr(VI) stock solution with adsorbents at room temperature. The influence of main operating parameters was explored, and the best proportion of the adsorbents was determined. Maximum sorption of Cr(VI) onto brown coal was observed at pH = 4 by adding 60 g L?1 adsorbent to contaminated solution. In case of using zeolite, the modification process was required, and the pH indicated a weak influence in a wide range (2–8). Optimum dosage of modified zeolite for Cr(VI) removal was 10 g L?1. The hybrid application of adsorbents with the mass ratio of brown coal/modified zeolite at (3:1) was capable of removing more than 99% of Cr(VI) from contaminated wastewater in the natural pH range of the wastewater. The adsorption of Cr(VI) by brown coal and modified zeolite followed Langmuir and Freundlich isotherm models, respectively. Sorption of Cr(VI) onto both brown coal and modified zeolite fitted well to pseudo-second-order rate reaction.  相似文献   

2.
Adsorption of Cr(VI) using native and chemically modified marine green macroalgae Codium tomentosum biomass and its adsorption kinetics were studied under specific conditions. Maximum Cr(VI) removal occurred at pH 2 for both untreated and acid-treated biomass. However, base-treated biomass exhibited maximum adsorption at pH 6 due to the hydrolysis of methyl esters present in the cellulose, hemicellulose and lignin molecules resulting in carboxyl groups (COO?) on the surface. The effect of adsorbent dose revealed that untreated and acid-treated biomass follows Henry’s linear isotherm, while base-treated biomass exhibited sigmoidal curve indicating energetic heterogeneity on the adsorbing surface. The monolayer adsorption capacity of untreated, acid-treated and base-treated biomasses was 5.032 ± 0.644, 5.445 ± 0.947, 3.814 ± 0.559 mg g?1, respectively. Adsorption was found to follow Ho and McKay’s pseudo-second-order kinetic model with decreasing pseudo-second-order rate constant (K 2, g mg?1 min?1) of 0.088 ± 0.037 (acid-treated), 0.019 ± 0.003 (untreated) and 0.012 ± 0.003 (base-treated).  相似文献   

3.
Microwave-assisted tetrabutyl ammonium-impregnated sulphate-crosslinked chitosan was synthesized for enhanced adsorption of hexavalent chromium. The adsorbent obtained was extensively characterized using Fourier transform infrared, X-ray diffraction, scanning electron microscopy and energy-dispersive X-ray studies. Various isotherm models such as Langmuir, Freundlich and Dubinin–Radushkevich were studied to comprehend the adsorption mechanism of hexavalent chromium by the adsorbent. Maximum adsorption capacity of 225.9 mg g?1 was observed at pH 3.0 in accordance with Langmuir isotherm model. The sorption kinetics and thermodynamic studies revealed that adsorption of hexavalent chromium followed pseudo-second-order kinetics with exothermic and spontaneous behaviour. A column packed with 1 g of adsorbent was found to give complete adsorption of Cr(VI) up to 900 mL of 200 mg L?1 solution which discerns the applicability of the adsorbent material for higher sample volumes in column studies. The effective adsorption results were obtained due to both ion exchange and ion pair interaction of adsorbent with hexavalent chromium. Greener aspect of overall adsorption was regeneration of the adsorbent which was carried out using sodium hydroxide solution. In the present study, the regenerated adsorbent was effectively reused up to ten adsorption–desorption cycles with no loss in adsorption efficiency.  相似文献   

4.
Batch sorption system using co-immobilized (activated carbon and Bacillus subtilis) beads as adsorbent was investigated to remove Cr(VI) from aqueous solution. Fourier transform infrared spectroscopy analysis showed the functional groups of both bacteria and activated carbon in co-immobilized beads. Experiments were carried out as a function of contact time (5–300 min), initial metal concentration (50–200 mg L?1), pH (2–8), and adsorbent dose (0.2–1 g L?1). The maximum percentage of removal was found to be 99 %. Langmuir model showed satisfactory fit to the equilibrium adsorption data of co-immobilized beads. The kinetics of the adsorption followed pseudo-second-order rate expression, which demonstrates that chemisorption plays a significant role in the adsorption mechanism. The significant shift in the Fourier transform infrared spectroscopy peaks and a Cr peak in the scanning electron microscope–energy dispersive spectroscopy spectra further confirmed the adsorption. The results indicate that co-immobilized beads can be used as an effective adsorbent for the removal of Cr(VI) from the aqueous solution.  相似文献   

5.
The adsorptive removal of Cr(VI) was studied using activated carbon derived from Leucaena leucocephala (ACLL). The physico-chemical properties of ACLL were determined using proximate analysis and N2 BET surface area analysis. The N2 BET surface area of ACLL was determined to be 1131 m2 g?1. The point of zero charge (pHpzc) of 5.42 indicated that ACLL surface was positively charged for pH below the pHPZC, attracting anions. The effect of experimental operating parameters such as time of contact, ACLL dose, pH, initial concentration and temperature was investigated. The optimum values of parameters such as concentration of 100 mg L?1, 300 mg of ACLL dose, time of contact of 60 min, pH of 4 indicated the maximum Cr(VI) uptake of 13.85 mg g?1. The pseudo-second-order kinetic model best fitted with the Cr(VI) adsorption data. Adsorptive removal of Cr(VI) onto ACLL satisfactorily fitted in the order of Redlich–Peterson > Freundlich > Langmuir > Temkin adsorption isotherm model. The thermodynamic parameters showed the adsorption of Cr(VI) onto ACLL was an endothermic and spontaneously occurred process.  相似文献   

6.
In this research, the stems of Onopordom Heteracanthom which is a kind of weed were converted to biochar particles, and their characteristics were investigated. The morphology and purity of these particles were examined by SEM and EDX techniques, respectively. Specific surface area was obtained as 5.73 m2 g?1 by BET method. The biochar particles obtained from Onopordom Heteracanthom were evaluated as an adsorbent to remove Cr(VI) from aqueous environments. The effect of some parameters such as initial concentration of Cr(VI), dosage of adsorbent, and pH were investigated on the adsorption capacity of Cr(VI) onto the adsorbent. The equilibrium data were analyzed by various isotherm models. The results revealed that in this process, the adsorption isotherm and kinetics have more conformity with Langmuir isotherm and pseudo-second-order kinetics, respectively. The multi-linearity of the Weber and Morris adsorption kinetic model indicates that the intra-particle diffusion is not merely the rate-controlling step for the whole adsorption process.  相似文献   

7.
Hexavalent chromium [Cr(VI)] is used in various industries, but its improper and uncontrolled discharge contaminates the environment. In order to circumvent chromium toxicity, several physicochemical and biological strategies have been employed. Among biological approach, microbes convert toxic Cr(VI) to less soluble Cr(III) form and hence can be used to detoxify/remove Cr(VI) from contaminated environment. Considering these, present study was designed to assess the effect of chromium reductases and antioxidants secreted by Penibacillus species to detoxify Cr(VI) and concurrently to augment soybean growth. Bacterial strains (MAI1 and MAI2) were identified as Penibacillus sp. using 16S rRNA gene. Penibacillus species reduced Cr(VI) significantly at pH 7. Maximum Cr(VI) was reduced at 50 and 100 µg/ml of Cr(VI) concentrations. Penibacillus sp. also reduced Cr(VI) significantly at 25 and 35 °C as well as 1 g sodium alginate in 1 g polyvinyl alcohol. Bacterial strains reduced Cr(VI) into Cr(III) which were detected as 33 ± 1 and 35 ± 1 µg/ml in supernatant and 67 ± 2.5 and 65 ± 1 µg/ml in cell debris, respectively, after 120 h. Chromium reductase found in cell-free extract reduced almost all Cr(VI) compared to those observed in cell debris. Both malondialdehyde and antioxidant levels were increased with gradual increase in Cr(VI) concentration. Penibacillus species inoculated soybean plants had better growth and photosynthetic pigments under Cr(VI) stress.  相似文献   

8.
The increasing emission of primary and gaseous precursors of secondarily formed atmospheric particulate matter due to continuing industrial development and urbanization are leading to an increased public awareness of environmental issues and human health risks in China. As part of a pilot study, 12-h integrated fine fraction particulate matter (PM2.5) filter samples were collected to chemically characterize and investigate the sources of ambient particulate matter in Guiyang City, Guizhou Province, southwestern China. Results showed that the 12-h integrated PM2.5 concentrations exhibited a daytime average of 51 ± 22 µg m?3 (mean ± standard deviation) with a range of 17–128 µg m?3 and a nighttime average of 55 ± 32 µg m?3 with a range of 4–186 µg m?3. The 24-h integrated PM2.5 concentrations varied from 15 to 157 µg m?3, with a mean value of 53 ± 25 µg m?3, which exceeded the 24-h PM2.5 standard of 35 µg m?3 set by USEPA, but was below the standard of 75 µg m?3, set by China Ministry of Environmental Protection. Energy-dispersive X-ray fluorescence spectrometry (XRF) was applied to determine PM2.5 chemical element concentrations. The order of concentrations of heavy metals in PM2.5 were iron (Fe) > zinc (Zn) > manganese (Mn) > lead (Pb) > arsenic (As) > chromium (Cr). The total concentration of 18 chemical elements was 13 ± 2 µg m?3, accounting for 25% in PM2.5, which is comparable to other major cities in China, but much higher than cities outside of China.  相似文献   

9.
In this study, teff (Eragrostis tef) straw has been chemically treated and tested as an adsorbent for Cr(VI) removal. Chemically treatment of teff straw was done by NaOH, H3PO4 and ZnCl2 solutions. Scanning electron micrograph and X-ray diffraction were used for anatomical characterization, whereas Fourier transform infrared spectroscopy was used for surface change characterization of adsorbents. Effects of different experimental parameters like pH (2–12), initial Cr(VI) concentration (100–900 mg/L), adsorbent dose (2.5–20 g/L), contact time (15–360 min) and temperature (288–318 K) were studied. Temperature increment was found to stimulate the adsorption process. Langmuir isotherm was found to give better representation over wide range of temperature for untreated, H3PO4- as well as ZnCl2-treated teff straw, and Freundlich isotherm best represented the isotherm data for NaOH-treated teff straw. Maximum Cr(VI) adsorption capacity of untreated, NaOH-, H3PO4- and ZnCl2-treated teff straw was found to be 86.1, 73.8, 89.3 and 88.9 mg/g, respectively. Respective values of average effective diffusion coefficient (D e) were found to be 2.8 × 10?13, 2.59 × 10?14, 1.32 × 10?13 and 1.14 × 10?13 m2/s, respectively. The negative value of ΔG o for all the adsorbents indicates Cr(VI) spontaneous adsorption. Isosteric heat of adsorption (ΔH st,a) was found to vary with surface coverage (θ). ΔH st,a increased for untreated, H3PO4- and ZnCl2-treated teff straw, and decreased steadily with θ for NaOH-treated teff straw.  相似文献   

10.
Plants and soils from central Euboea, were analyzed for Cr(totai), Cr(VI), Ni, Mn, Fe and Zn. The range of metal concentrations in soils is typical to those developed on Fe-Ni laterites and ultramafic rocks. Their bioavailability was expressed in terms of concentrations extractable with EDTA and 1 M HNO3, with EDTA having a limited effect on metal recovery. Cr(VI) concentrations in soils evaluated by alkaline digestion solution were lower than phytotoxic levels. Chromium and Ni — and occasionally Zn — in the majority of plants were near or above toxicity levels. Cr(VI) concentrations in plants were extremely low compared to total chromium concentrations. Cr(total) in ground waters ranged from <1 μg.L?1 to 130 μg.L?1, with almost all chromium present as Cr(VI). With the exception of Cr(total) and in some cases Zn, all elements were below regulatory limits for drinking water. On the basis of Ca, Mg, Cr(total) and Si ground waters were classified into three groups: Group(I) with Cr concentrations less than 1 μg.L?1 from a karstic aquifer; Group(II) with average concentrations of 24 μg.L?1 of Cr and relatively high Si associated with ophiolites; and Group(III) with Cr concentrations of up to 130 μg.L?1, likely due to anthropogenic activity. Group(III) is comparable to ground waters from Assopos basin, characterized by high Cr(VI) concentrations, probably due to industrial actrivities.  相似文献   

11.
Tropical peat soils present higher ash content than those generated at temperate climate areas. Therefore, this study evaluated the characteristics of a Brazilian organic soil (OS), commercialized as peat, as well as its capacity in removing Cr(VI) from contaminated waters. The OS is composed of 35.5 wt% of organic matter and 56 wt% of inorganic fraction (ash), which is formed by minerals and phytoliths rich in silica (29.2 wt%) and alumina (23.6 wt%). The Cr(VI) removal tests were carried out in batch and column systems using OS and solutions of Cr(VI) prepared with distilled water and groundwater. Batch tests revealed that the organic substances in the OS caused the reduction of Cr(VI) to Cr(III), with an efficiency depending on solution pH. At pH 5.0 the Cr(VI) removal was 0.45 mg g?1 in 24 h; whereas at pH 2.0, this removal increased to 1.10 mg g?1. Since this redox reaction is very slow, the removal of Cr(VI) at pH 5.0 increased to around 2 mg g?1 after 5 days. The removal of Cr(VI) was more effective in the column tests than in the batch test due to the greater solid/solution ratio, and their half-lives were 4.4 and 26.2 h, respectively. Chemical analysis indicated that Cr(VI) was reduced by the humic substances of OS, followed by the precipitation and/or adsorption of Cr(III) into the organic and inorganic components, as anatase. The presence of Cr(III) increased the stability of anatase structure, avoiding its transformation into rutile, even after being heated at 800 °C/2 h.  相似文献   

12.
This study presents the results of chromate adsorption upon organically modified clinoptilolite obtained by the treatment of Bigadic clinoptilolite with surfactants in primary amine structure, namely 1-dodecylamine, 1-hexadecylamine and oleylamine. Natural and organo-clinoptilolites were characterized by X-ray diffraction, thermal gravimetry and Fourier transform infrared spectrometry which proved the integration of amine groups followed by the order oleylamine > 1-hexadecylamine > 1-dodecylamine. Organo-clinoptilolites were tested for their efficacy in chromate removal under base case conditions which implied 100 ppm initial concentration, pH 4.0, 10 g l?1 adsorbent dose and at 298 K. Results showed that amine loading induced chromate removal reaching up to 90 % for oleylamine-modified clinoptilolite. Experimentation was continued to determine the effects of pH, adsorbent dosage and initial concentration on chromate adsorption. Accordingly, maximum removal of 94.0 % was attained with 14 g l?1 of oleylamine-modified clinoptilolite, from Cr(VI) solution of 100 ppm initially at pH 3.0. Langmuir isotherm described the adsorption of chromate on oleylamine-modified clinoptilolite with 96.4 % consistency. Maximum theoretical uptake capacity was calculated as 6.72 mg g?1. Kinetic data were consistent with pseudo-second-order model with the controlling steps being film and pore diffusions.  相似文献   

13.
Pannonibacter phragmitetus BB was utilized to treat hexavalent chromium [Cr(VI)] contaminated water. Cr(VI) concentration of the contaminated water (pH 10.85) was 534 mg/L. With the inoculum size ranging from 1 to 20 %, P. phragmitetus BB completely reduced Cr(VI) within 27 h when the initial medium concentration exceeded 20 g/L. The lag time of bio-reduction by Cr(VI)-induced cells was 24 h, which was longer than the non-Cr(VI)-induced cells. Under the agitation condition, an obvious bio-reduction lag phase existed and Cr(VI) was completely reduced within 24 h. However, the lag phase was not observed under the static condition, Cr(VI) was reduced continuously after inoculation and Cr(VI) was completely reduced after 27 h incubation. The main chromium components after Cr(VI) reduction were Cr(OH)3, Cr2O3 and CrCl3. The results of this study are fundamentally significant to the application of P. phragmitetus BB in the treatment of Cr(VI) contaminated water.  相似文献   

14.
In this study, arsenic as an environmental top-ranked hazardous substance was efficiently removed by a novel adsorbent fabricated by magnetite Fe3O4 nanoplates decorated on anodized aluminum oxide (AAO) nanofibers. AAO nanofibers were prepared by anodic polarization method, and then Fe3O4 nanoplates were grown on AAO-based substrate by hydrothermal method to fabricate AAO/Fe3O4 nanosorbent. Morphology of the fabricated adsorbents was characterized by field emission scanning electron microscopy (FE-SEM), and their crystallinity was studied by X-ray diffraction (XRD). Arsenic (III) removal potential of the proposed adsorbent from contaminated water samples was investigated by the determination of As(III) amounts in the samples by inductively coupled plasma optical emission spectroscopy before and after adsorption process at sub-μg L?1 levels. The results showed that without pre- and post-treatments such as pH adjustment, As(III) was removed effectively from contaminated water samples by using the proposed adsorbent. AAO/Fe3O4 sorbent showed excellent ability to remove 0.1 mg L?1 As(III) from water samples up to 96 % uptake. Freundlich adsorption isotherm model was used to interpret the As(III) adsorption on proposed sorbent. The Freundlich isotherm parameters n and k F were obtained to be 2.2 and 10.2, respectively, representing the high affinity of proposed adsorbent for arsenic removal.  相似文献   

15.
The redox-sensitive stable isotope geochemistry of chromium bears the potential to monitor the attenuation of chromate pollution and to investigate changes in environmental conditions in the present and the past. The use of stable Cr isotope data as a geo-environmental tracer, however, necessitates an understanding of the reaction kinetics and Cr fractionation behaviour during redox transition and isotope exchange. Here, we report stable chromium isotope fractionation data for Cr(VI) reduction, Cr(III) oxidation and isotopic exchange between soluble Cr(III) and Cr(VI) in aqueous media. The reduction of Cr(VI) to Cr(III) with H2O2 under strongly acidic conditions shows a near-equilibrium isotope fractionation of Δ53/52Cr(Cr(III)-Cr(VI)) of −3.54 ± 0.35‰. At pH neutrality, however, the reduction experiments show a kinetic isotope fractionation Δ53/52Cr(Cr(III)-Cr(VI)) of −5‰ for the extent of reduction of up to 85% of the chromium. The oxidation of Cr(III) to Cr(VI) in alkaline media, using H2O2 as the oxidant, cannot be explained by a single, unidirectional reaction. Our experiments indicate that the involvement of the unstable intermediates Cr(IV) and Cr(V) and their disproportionation during redox reactions between Cr(III) and Cr(VI) influence the overall fractionation factor, depending on the prevailing pH conditions and the reaction rates. No detectable isotope exchange between soluble Cr(VI) and Cr(III) species at pH values of 5.5 and 7 was revealed over a timescale of days to weeks. This means that, at least within such a time frame, the isotopic composition of Cr(VI) in a natural system will not be influenced by equilibration with any Cr(III) and thus reveal the true extent of reduction, given that the Cr isotope composition of the source Cr(VI) and the fractionation factor for the prevailing conditions are known.  相似文献   

16.
Hexavalent chromium has been proved to be the reason of several health hazards. This study aimed at evaluating the application of pomegranate seeds powder for chromium adsorption (VI) from aqueous solution. Chromium adsorption percentage (VI) increased with increasing the adsorbent dosage. Chromium adsorption capacity (VI), at pH = 2 and 10 mg/L initial metal concentration, decreased from 3.313 to 1.6 mg/g through increasing dosage of adsorbent from 0.2 to 0.6 g/100 ml. The adsorption rate increased through increase in chromium initial concentration (VI). However, there was a removal percentage reduction of chromium (VI). Chromium adsorption kinetics by different models (pseudo-first-order, modified pseudo-first-order, pseudo-second-order, Elovich, intraparticle diffusion, Boyd kinetic) was investigated as well. Studies on adsorption kinetic indicated that the experimental data were matched by pseudo-second-order model (R 2 = 0.999) better. Obtained results demonstrated the pomegranate seeds can be used as an effective biomaterial and biosorbent for hexavalent chromium adsorption from aqueous solutions.  相似文献   

17.
In this work, a low-cost lignocellulosic adsorbent with high biosorption capacity is proposed, suitable for the efficient removal of hexavalent chromium from water and wastewater media. The adsorbent was produced by autohydrolyzing Scots Pine (Pinus Sylvestris) sawdust. The effect of the autohydrolysis conditions, i.e., pretreatment time and temperature, on hexavalent chromium biosorption was investigated using energy-dispersive X-ray spectroscopy (EDS) and UV–visible spectrophotometry. The Freundlich, Langmuir, Sips, Radke-Prausnitz, Modified Radke-Prausnitz, Tóth, UNILAN, Temkin and Dubinin-Radushkevich adsorption capacities and the rate constant values for pseudo-first- and pseudo-second-order kinetics indicated that the autohydrolyzed material exhibits significantly enhanced hexavalent chromium adsorption properties comparing with the untreated sawdust. The Freundlich’s adsorption capacity K F increased from 2.276 to 8.928 (mg g?1)(L mg?1)1/n , and the amount of hexavalent chromium adsorbed at saturation (Langmuir constant q m) increased from 87.4 to 345.9 mg g?1, indicating that autohydrolysis treatment at 240 °C for 50 min optimizes the adsorption behavior of the lignocellulosic material.  相似文献   

18.
The discharge of industrial effluents containing hexavalent chromium can be very harmful for the environment. Therefore, Cr(VI) should be removed from contaminated water, and especially from wastewater, to prevent its discharge into the environment. This study is aimed at analyzing the factors that affect the removal of Cr(VI) with the use of almond green hull and ash adsorbent. The effects of pH (2–10), adsorbent dose (2–24 g/L), Cr(VI) concentration (10–100 mg/L), exposure time (1–60 min), and temperature (5–50 °C) were examined. The surface morphology, pore size of adsorbent surfaces were characterized with SEM, EDX, FTIR. Maximum removal occurred at pH = 2. Results showed that the removal yield increased with the rise of exposure time and temperature. The data indicate that due to limited site on adsorbent surface, the removal efficiency decreased as initial Cr(VI) concentration increased. When the adsorbent dose was increased, the removal yield increased in the case of the bioadsorbent as well; however, in the ash adsorbent, there was an increase followed by a decreasing trend. The study highlights that almond green hull can be more efficient than its ash in the removal of Cr(VI) from aqueous solution. As a general result of study, it can be argued that almond green hull bioadsorbent and the obtained carbon are able to remove Cr(VI) from aqueous solutions; thus, they can be used as efficient and economical substitutes for existing adsorbents like activated carbon, for the removal of chromium from polluted aqueous solutions.  相似文献   

19.
The pollution of soil with heavy metals has direct or indirect adverse effect on human health. The present work was conducted to identify all the expected sources and sinks for heavy metals by applying mass balance model to identify the retention rate of metals by soils in Yaakob village, south Sohag Governorate, Egypt. The studied inputs (sources) include P-fertilizers, irrigation water and dustfall, while the main outputs (sinks) are drainage water and harvested plants. The measurements indicate that soil, clover, dustfall and P-fertilizers contain considerable concentration of Cd, Cr, Co, Cu and Pb. The mass balance measurements indicate that the accumulation rate of Cd, Cr and Co in soil was 5.4, 54.6 and 16.3 g ha?1 year?1, respectively. However, depletion trend of Pb and Cu was about 1.4 and 5.2 g ha?1 year?1, respectively. The main source of Cd, Pb, Cr and Co in the study area is P-fertilizers with input flux 14.9, 89.9, 198.6 and 18.5 g ha?1 year?1, while Cu source was dustfall with 19.33 g ha?1 year?1. The index of geoaccumulation calculations indicates different degrees of contamination with Cd, Cr, Co and Cu. On the other hand, the main sink for the studied heavy metals was the Egyptian clover (Trifolium alexandrinum) which can be considered a good bioaccumulator of heavy metals.  相似文献   

20.
Three chromium-resistant bacteria Bacillus pumilus-S4, Pseudomonas doudoroffii-S5 and Exiguobacterium-S8 were isolated from chromium-contaminated wastewater/soil and could resist very high concentrations of potassium chromate in Luria agar (up to 25 mg ml?1) and acetate minimal medium (2 mg ml?1). The strains showed growth at diverse pH and temperatures and could resist multiple heavy metals. Pseudomonas doudoroffii-S5 reduced (8.27 mg hexavalent chromium 24 h?1) at a lower initial potassium chromate concentration (100 μg ml?1), but overall more chromate (28.4 mg hexavalent chromium 24 h?1) was reduced at a higher initial concentration (1,000 μg ml?1). The addition of various heavy metals (zinc sulphate, copper sulphate, and manganese sulphate at 50 μg ml?1) in the chromium reduction media did not significantly affect the hexavalent chromium reduction potential of these isolates. The chromium removal/detoxification potential of these strains increased when used in conjunction with hydrophytes Eichornia crassipes and Pistia stratiotes. Interestingly, the whole process runs automatically with less energy input, that is, the bacterial strains support the growth of plant while in turn the plant releases exudates that help bacterial growth.  相似文献   

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