Efficient selective adsorption of Cr(VI) by S-doped porous carbon prepared from industrial lignin: Waste increment and wastewater treatment.

Industrial lignin is a waste product of the paper industry, which contains a large amount of oxygen group structure, and can be used to treat industrial wastewater containing Cr(VI). However, lignin has very low reactivity, so how to enhance its adsorption performance is a major challenge at present. In this study, a two-stage hydrothermal and activation strategy was used to activate the lignin activity and doping S element to prepare high-performance S-doped lignin-based polyporous carbon (S-LPC). The results show that the surface of S-LPC is rich in S and O groups and has a well-developed pore structure, which is very beneficial to Cr(VI) uptake -reduction and mass transfer on the material. In the wastewater, the utmost adsorption potential of Cr(VI) by S-LPC achieved 882.83 mg/g. After 7 cycles of regeneration, the adsorption of S-LPC decreased by only approximately 18 %. Ion competition experiments showed that S-LPC has excellent specificity for Cr(VI) adsorption. In factory wastewater, the adsorption performance of S-LPC for Cr(VI) remained above 95 %, which shows the excellent performance of S-LPC in practical applications. The results are of great significance for green chemical utilization of waste lignin, treatment of industrial wastewater and sustainable development.

Modeling of hexavalent chromium removal onto natural zeolite from air stream in a fixed bed column.

The increasing use of hexavalent chromium (Cr(VI)) has exposed large populations to this environmental and occupational carcinogenic agent. Therefore, researchers have been interested in removing this substance through adsorbents. This study aimed to investigate the efficiency of natural zeolite in the direct adsorption of Cr(VI) from airflow and its adsorption modeling. In this study, a nebulizer device produced the Cr(VI) mist. The efficiency of natural zeolite in Cr(VI) adsorption from airflow, modeling of fixed column adsorption, and the effective parameters on adsorption efficiency including the initial concentration of chromium, airflow rate, and adsorption bed depth were studied. To facilitate the prediction of the performance of natural zeolite's adsorption column, Yoon-Nelson, Thomas, BDST, and Buhart-Adams models were used. The results showed that the adsorption capacity diminished with increased airflow rate and initial concentration, while it increased with elevated height of the adsorption bed. Yoon-Nelson, Thomas, and BDST models corresponded to experimental data with a correlation coefficient of 0.9933, but the information of the Buhart-Adams model had a lower correlation coefficient (around 0.6677). In conclusion, natural zeolite can be used as an efficient low-cost adsorbent for directly Cr(VI) removing from the airflow in a fixed bed column.

Efficient removal of Chromium(VI) from wastewater based on magnetic multiwalled carbon nanotubes coupled with deep eutectic solvents.

Industrial wastewater containing heavy metal Cr(VI) seriously affects the health of organisms and may even lead to cancer. Developing efficient adsorbents that can quickly separate heavy metals is crucial for treating wastewater. In this study, magnetic multiwalled carbon nanotubes (MMWCNTs) with moderate particle size and abundant surface active sites were prepared by coating multiwalled carbon nanotubes with magnetic nanoparticles. The results of FTIR, XRD, TG, VSM, BET, and EDS showed MWCNTs completely encapsulated on the surface of the magnetic nanoparticles, with a particle size of approximately 30 nm. Oxygenated groups provided abundant surface active sites and formed numerous mesopores. The response surface methodology was used to optimize the adsorbent dose, adsorption contact time and adsorption temperature, and the removal rate of Cr(VI) was more than 95%. The quasi-second order kinetics and Freundlich adsorption isotherm model explained the adsorption process to Cr(VI). MMWCNTs interacted with Cr(VI) through electrostatic attraction, reduction reactions, complexation, and other means. The extensive hydrogen bonding of the green solvent deep eutectic solvent (DES) was employed to desorb the MMWCNTs and desorption rate exceed 90%. Even after five adsorption-regeneration cycles, the adsorbent maintained a high capacity. In conclusion, these novel MMWCNTs, as efficient adsorbents paired with DES desorption, hold broad potential for application in the treatment of Cr(VI)-contaminated wastewater.

Design, preparation, and performance of different adsorbents based on carboxymethyl chitosan/sodium alginate hydrogel beads for selective adsorption of Cadmium (II) and Chromium (III) metal ions.

Developing cost-effective and efficient adsorbents for heavy metals in multicomponent systems is a challenge that needs to be resolved to meet the challenges of wastewater treatment technology. Two adsorbents were synthesized, characterized, and investigated for the removal of Cd2+ and Cr3+ as model heavy metals in their single and binary solutions. The first adsorbent (ACZ) was a nanocomposite formed of O-Carboxymethyl chitosan, sodium alginate, and zeolite. While, the other (ACL) contained ZnFe layered double hydroxides instead of the zeolite phase. Adsorbents were characterized using XRD, FTIR, SEM, and swelling degree analysis. For single heavy metal adsorption isotherms, data for both adsorbents was best fitted and indicated a multilayer adsorption nature. For binary adsorption, Langmuir model with interacting parameters showed the best results compared to other models for both pollutants. For single system, Avrami model was found to be the best model representing the adsorption kinetics data, which indicates that the mechanism of adsorption follows multiple kinetic orders that may change during duration of adsorption process. Numerous interaction mechanisms can occur between the heavy metals and functional groups in the synthesized hydrogels such as NH2, COOH, and OH groups leading to efficient adsorption of metal ions.

In situ carbothermal synthesis of carbonized bacterial cellulose embedded with nano zero-valent iron for removal of Cr(VI).

Carbonized bacterial cellulose embedded with highly dispersed nano zero-valent iron (nZVI), denoted as nZVI@CBC, was prepared through one-step in situ carbothermal treatment of bacterial cellulose adsorbing iron(III) nitrate. The structure characteristics of nZVI@CBC and its performance in removing hexavalent chromium Cr(VI) were investigated. Results showed the formation of nZVI@CBC with a surface area of 409.61 m2/g at 800 °C, with nZVI particles of mean size 28.2 nm well distributed within the fibrous network of CBC. The stability of nZVI was enhanced by its carbon coating, despite some inevitable oxidation of exposed nZVI. Batch experiments demonstrated that nZVI@CBC exhibited superior removal efficiency compared to bare nZVI and CBC. Under optimal conditions, nZVI@CBC exhibited a high Cr(VI) adsorption capacity of up to 372.42 mg/g. Therefore, nZVI@CBC shows promise as an effective adsorbent for remediating Cr(VI) pollution in water.

Polysaccharide-based (nano)materials for Cr(VI) removal.

Chromium is a potentially poisonous and carcinogenic species, which originates from human activities and various industries such as leather, steel, iron, and electroplating industries. Chromium is present in various oxidation states, among which hexavalent chromium (Cr(VI)) is highly toxic as a natural contaminant. Therefore, chromium, particularly Cr(VI), must be eliminated from the environment, soil, and water to overcome significant problems due to its accumulation in the environment. There are different approaches such as adsorption, ion exchange, photocatalytic reduction, etc. for removing Cr(VI) from the environment. By converting Cr(VI) to Cr(III), its toxicity is reduced. Cr(III) is essential for the human diet, even in small amounts. Today, biopolymers such as alginate, cellulose, gum, pectin, starch, chitin, and chitosan have received much attention for the removal of environmental pollutants. Biopolymers, particularly polysaccharides, are very useful compounds due to their OH and NH2 functional groups and some advantages such as biodegradability, biocompatibility, and accessibility. Therefore, they can be widely applied in catalytic applications and as efficient adsorbents for the removal of toxic compounds from the environment. This review briefly investigates the application of polysaccharide-based (nano)materials for efficient Cr(VI) removal from the environment using adsorption/reduction, photocatalytic, and chemical reduction mechanisms.

Identification of metal binding motifs in protein frameworks to develop novel remediation strategies for Hg2+ and Cr(VI).

Amino acid sequences in metal-binding proteins with chelating properties offer exciting applications in biotechnology and medical research. To enhance their application in bioremediation studies, we explicitly aimed to identify specific metal-binding chelating motifs in protein structures for two significant pollutants, such as mercury (Hg2+) and chromium Cr(V1). For this purpose, we have performed an extensive coordination chemistry approach by retrieving Hg2+ and Cr(V1) binding protein structures from the protein database and validated using the B-factor, a term defining uncertainty of the atoms and with occupancy to obtain the best binding motifs. Our analysis revealed that acidic amino acids like aspartic acid, glutamic acid, and basic amino acids such as cysteine and histidine are predominant in coordinating with these metals. The order of preference in Hg2+-bound structures is predicted to be Cys > His > Asp > Glu, and for Cr(V1) is His > Asp > Glu. Examination of the atomic coordinates and their distance from each metal revealed that the sulfur atoms of cysteine showing more preference towards Hg2+coordination with an atomic distance ranging from 1.5 to 2.9 Å. Likewise, oxygen atoms of aspartic acid, glutamic acid and nitrogen atoms of histidine are within 2 Å of Cr(V1) coordination. Based on these observations, we obtained C-C-C, C-X(2)-C-C-(X)2-C, H-C-H motifs for Hg2+, and D-X(1)-D, H-X(3)-E motif for Cr(V1) to be shared within the coordination space of 3 Å. As a future scope, we propose that the identified metal-binding chelating motifs are oligopeptides and can display on the surface of microorganisms such as Escherichia coli and Saccharomyces cerevisiae for effective removal of natural Hg2+ and Cr(V1) through biosorption. Hence, our results will provide the basis for futuristic bioremediation.

Microbial Sensing and Removal of Heavy Metals: Bioelectrochemical Detection and Removal of Chromium(VI) and Cadmium(II).

The presence of inorganic pollutants such as Cadmium(II) and Chromium(VI) could destroy our environment and ecosystem. To overcome this problem, much attention was directed to microbial technology, whereas some microorganisms could resist the toxic effects and decrease pollutants concentration while the microbial viability is sustained. Therefore, we built up a complementary strategy to study the biofilm formation of isolated strains under the stress of heavy metals. As target resistive organisms, Rhizobium-MAP7 and Rhodotorula ALT72 were identified. However, Pontoea agglumerans strains were exploited as the susceptible organism to the heavy metal exposure. Among the methods of sensing and analysis, bioelectrochemical measurements showed the most effective tools to study the susceptibility and resistivity to the heavy metals. The tested Rhizobium strain showed higher ability of removal of heavy metals and more resistive to metals ions since its cell viability was not strongly inhibited by the toxic metal ions over various concentrations. On the other hand, electrochemically active biofilm exhibited higher bioelectrochemical signals in presence of heavy metals ions. So by using the two strains, especially Rhizobium-MAP7, the detection and removal of heavy metals Cr(VI) and Cd(II) is highly supported and recommended.

Iron oxides decorated graphene oxide/chitosan composite beads for enhanced Cr(VI) removal from aqueous solution.

This study is the first to evaluate the effects of Iron oxides (FeOx) species and their decoration on graphene oxide/chitosan (GO/CS) composites for Cr(VI) removal and the possibility of Fe secondary pollution. Results show that Fe(III) is a better decoration material than Fe(II) and decoration through immersion-evaporation shows a higher adsorption capacity of Cr(VI) (Qe) than co-precipitation. Fe2O3-GO/CS as the only eco-friendly composite for enhanced Cr(VI) removal is further used for batch adsorption experiments, characterization, kinetics, isotherms, and thermodynamic studies. It is found that Cr(VI) removal mainly includes electrostatic attraction between Cr(VI) oxyanions and surface -NH3+ and -OH2+, and the adsorbed Cr(VI) partially reduces to Cr(III). Qe increases with the increasing initial Cr(VI) concentration, contact time, and temperature, while decreases with the increasing pH and mass and volume ratio (m/v). The coexisting ions (Cl-, NO3-, SO42-, PO43-, As, Fe, and Pb) can cause an obvious decrease of Qe. The removal efficiency (Re) and Qe are 94.3% and 83.8 mg/g, respectively under the optimal conditions. After five times of regeneration, Re is still as high as 84% and Qe drops about 2.6%. Cr(VI) adsorption is spontaneous and endothermic, which is best fitted with the Sips model, and the fitted maximum Qe is 131.33 mg/g.

Preparation of highly dispersive and antioxidative nano zero-valent iron for the removal of hexavalent chromium.

In this study, carboxymethyl cellulose (CMC) was employed to stabilize zero-valent iron nanoparticles (CMC-nFe0) to improve their dispersity and antioxidation for enhanced hexavalent chromium (Cr(VI)) removal. Scanning electron microscope (SEM) observation revealed that the nFe0 agglomerated in clusters, while the CMC-nFe0 connected as chains and presented higher dispersity. Therefore, compared with 54% of the nFe0, the Cr(VI) removal rate of the CMC-nFe0 increased by 0.8 time, reaching 97%. Besides, the nFe0 precipitated in 1 d and was obviously oxidized within 7 d under anoxic condition, leading to a rapid decease of Cr(VI) removal efficiency from 54% to 3% in 56 d. In contrast, the CMC-nFe0 showed no obvious subsidence and oxidized phenomenon within 14 d, which retained a relatively high Cr(VI) removal efficiency of 63% in 56 d, contributing to effective blockage of dissolved oxygen infiltrating from solution to nFe0 particles in presence of CMC. After reaction, the valence state distribution of Cr between solution and material surface indicated that Cr(VI) reduction was dominant comparing to physical adsorption to particles in the remediation process conducted by CMC-nFe0. In addition, lower initial pH and higher iron dosage facilitated Cr(VI) removal. Those results indicated that the dispersive and antioxidative characteristics of CMC-nFe0 were significantly superior to those of nFe0, and CMC stabilization thereafter can be a promising method to promote Cr(VI) elimination by nFe0.

Enhancement of the chromium removal behavior of Moringa oleifera activated carbon by chitosan and iron oxide nanoparticles from water.

The effect of chitosan and Fe3O4 magnetic nanoparticles on the chromium adsorption property of Moringa oleifera activated carbon (AC) was explored. Various techniques were applied to reveal the properties of adsorbers to absorb chromium ions. A majority of the pollutant was removed at pH2 and 50 min. The kinetic behavior of the chromium uptake process was governed by the pseudo-second-order kinetic model (PSOKM). Based on the thermodynamic investigation, the chromium adsorption using all adsorbers was exothermic and spontaneous. The maximum single-layer adsorption capacity of AC, CS/AC, AC/Fe3O4, and CS/AC/Fe3O4 adsorbers was 56.78 mg/g, 114.80 mg/g, 121.70 mg/g, and 130.80 mg/g, respectively. The isotherm constants quantity highlighted that the Cr-adsorption process is optimal and physical. The acquired findings revealed that the modification of AC by chitosan and Fe3O4 nanoparticles increased the Cr adsorption. Adsorbers re-used up to 5 stages with a yield >90 %, which indicates that the composites are a promising option for Cr removal.

Capture and Release Recyclable Dimethylaminomethyl-Calixarene Functional Cloths for Point-of-Use Removal of Highly Toxic Chromium Water Pollutants.

Chromium(VI) contamination of drinking water arises from industrial activity wherever there is a lack of environmental legislation enforcement regarding the removal of such pollutants. Although it is possible to remove such harmful metal ions from drinking water through large-scale facilities, there currently exists no safe and simple way to filter chromium(VI) oxoanions at the point of use (which is potentially safer and necessary in remote locations or humanitarian scenarios). High-surface-area cloth substrates have been functionalized with calixarene molecules for the selective capture of aqueous chromium(VI) oxoanions in the presence of structurally similar anions. This is accomplished by pulsed plasmachemical deposition of a linker layer and subsequent functionalization with dimethylaminomethyl-calixarene (5,11,17,23-tetrakis[(dimethylamino)methyl]-25,26,27,28-tetrahydroxycalix[4]arene). Chromium(VI) oxoanions are captured by simply passing polluted water through the functionalized cloth, while other ions not harmful/beneficial to human health remain in the water. These cloth filters are simple to use, highly selective, and easily recyclable-thus making them attractive for point-of-use application in geographic regions lacking appropriate wastewater treatment plants or flawed environmental monitoring systems. Chromium(VI) pollutants have been successfully removed from real-world contaminated industrial wastewater streams using the dimethylaminomethyl-calixarene functionalized cloths.

Ultraviolet Carbon Nanodots Providing a Dual-Mode Spectral Matching Platform for Synergistic Enhancement of the Fluorescent Sensing.

The sensing of chromium(VI) (Cr(VI)) is highly desired, due to its toxic and carcinogenic effects upon human health. Fluorescent probes, especially carbon nanodots (CNDs), have been widely used for Cr(VI) sensing via the inner filter effect (IFE). However, improving the sensitivity of these probes remains a difficult issue. In this work, CNDs derived from ß-Lactoglobulin were applied as an ultrasensitive fluorescent probe for Cr(VI). With 260 nm excitation, the CNDs showed multi-band emission, including an ultraviolet 360 nm peak. The spectral matching of the CNDs with Cr(VI) led to synergistic suppression of both the excitation and emission light in the fluorescent sensing. As a consequence, the CNDs showed high sensitivity toward Cr(VI), the detection limit reaching as low as 20 nM. Moreover, taking advantage of the multi-emissive property of the CNDs, the synergistic effect was proven in an IFE-based sensing system, which might be extended to the design of other kinds of fluorescent probes.

An ex-situ and in vitro approach towards the bioremediation of carcinogenic hexavalent chromium.

Chromium, ranking the second most among toxic heavy metal pollutants in the world, causing respiratory, cardiovascular and renal problems in human beings is under study herein. We examined the biological remediation of the carcinogenic Cr (VI) polluted soils by indigenous yeast isolates. The total element analysis of the treated sample was determined by Energy Dispersion X-ray Micro Analysis (EDXMA). The sample under study was observed to have a high concentration of 458.29 mgKg-1 Cr (VI), determined by Atomic Absorption Spectroscopy (AAS) and DPC analysis. The most tolerant isolate designated as CSR was used for in vitro and ex-situ bioremediation studies of Cr (VI). The isolate achieved significant bioremediation of 86% in vitro and 75.12% in ex-situ method. The optimal conditions for in vitro bioremediation were found to be 28 °C and a pH of 6. The ITS1, 5.8S rRNA and D1, D2 domain of LSU rRNA gene characterization of the isolate CSR illustrated that it belongs to Ustilago genera. The isolate was deposited in NCBI GenBank as Ustilago sp. CSR (KY284846). Although, Ustilago is generally a pathogenic fungus, our study opens up the scope of using Ustilago spp. for bioremediation of the carcinogenic heavy metal Chromium.

Effect of biochar modified with magnetite nanoparticles and HNO3 for efficient removal of Cr(VI) from contaminated water: A batch and column scale study.

Chromium (Cr) poses serious consequences on human and animal health due to its potential carcinogenicity. The present study aims at preparing a novel biochar derived from Chenopodium quinoa crop residues (QBC), its activation with magnetite nanoparticles (QBC/MNPs) and strong acid HNO3 (QBC/Acid) to evaluate their batch and column scale potential to remove Cr (VI) from polluted water. The QBC, QBC/MNPs and QBC/Acid were characterized with SEM, FTIR, EDX, XRD as well as point of zero charge (PZC) to get an insight into their adsorption mechanism. The impact of different process parameters including dose of the adsorbent (1-4 g/L), contact time (0-180 min), initial concentration of Cr (25-200 mg/L) as well as solution pH (2-8) was evaluated on the Cr (VI) removal from contaminated water. The results revealed that QBC/MNPs proved more effective (73.35-93.62-%) for the Cr (VI) removal with 77.35 mg/g adsorption capacity as compared with QBC/Acid (55.85-79.8%) and QBC (48.85-75.28-%) when Cr concentration was changed from 200 to 25 mg/L. The isothermal experimental results follow the Freundlich adsorption model rather than Langmuir, Temkin and Dubinin-Radushkevich adsorption isotherm models. While kinetic adsorption results were well demonstrated by pseudo second order kinetic model. Column scale experiments conducted at steady state exhibited excellent retention of Cr (VI) by QBC, QBC/MNPs and QBC/Acid at 50 and 100 mg Cr/L. The results showed that this novel biochar (QBC) and its modified forms (QBC/Acid and QBC/MNPs) are applicable with excellent reusability and stability under acidic conditions for the practical treatment of Cr (VI) contaminated water.

Remediation of hexavalent chromium contaminated water through zero-valent iron nanoparticles and effects on tomato plant growth performance.

Contaminated water with hexavalent chromium Cr(VI) is a serious environmental problem. This study aimed to evaluate the Cr(VI) removal by zero valent iron nanoparticles (nZVI) reduction process and the impact of Cr(VI), nZVI and combined treatment with nZVI and Cr(VI) on tomato growth performance. To evaluate the Cr(VI) toxic effect on germination capability, seeds were exposed to increasing Cr(VI) concentrations up to 1000 mg L-1. The inhibition of seed germination and the decrease of hypocotyl and root length started from Cr(VI) 5 mg L-1. Under treatment with Cr(VI) + nZVI 5 mg L-1, seed germination, hypocotyl and root length resulted significantly higher compared to Cr(VI) 5 mg L-1 treatment. The impact of only nZVI was investigated on chlorophyll and carotenoid in leaves; iron levels in leaves, roots, fruits and soil; carotenoid, fat-soluble vitamin and nicotianamine in mature fruits. A significant increase of leaf chlorophyll and carotenoids was observed after nZVI 5 mg L-1 treatment compared to controls. No significant variations were observed in carotenoids, fat-soluble vitamins and nicotianamine levels after treatment with nZVI 5 mg L-1 in mature fruits. For their ability to reduce Cr(VI) and to stimulate tomato growth, nZVI might to be considered as alternative for remediation purposes.

An ion release controlled Cr(VI) treatment agent: Nano zero-valent iron/carbon/alginate composite gel.

A simple iron/carbon composite was prepared by ion exchange and carbothermal reduction, and the characterization results showed that this material contained a large amount of nanoscale zero-valent iron. Then above material was coated with alginate to form a stable gel, which combined adsorption and reduction to remove Cr(VI) efficiently and controllably. The experiment showed that the optimal conditions for Cr(VI) removal were pH value, dosage and Cr(VI) concentration of 2, 2 g L-1 and 20 mg L-1, respectively. For 150 mL of 20 mg L-1 Cr(VI) solution, the removal efficiency could reach 100% in 6 h (dosage: 2 g L-1). Compared with activated carbon-alginate complex and pure alginate, the introduction of nanoscale zero-valent iron greatly accelerated the rate of Cr(VI) removal. In addition, adsorption isotherm and kinetics conformed to Freundlich and Elovich model, respectively. Under pH 2, the release of iron ion increased linearly with time and reached 51.87 mg L-1 in 8 h. The mechanism of Cr(VI) removal of iron/carbon composite coated with alginate might be controlled by two steps: the initial adsorption and fixation, and subsequent reduction. In general, the material is efficient, recyclable and controllable, which provides a new idea for the treatment of chromium-containing wastewater.

Polyethylene glycol-stabilized nano zero-valent iron supported by biochar for highly efficient removal of Cr(VI).

In this study, polyethylene glycol (PEG)-stabilized nano zero-valent iron (nZVI) supported by biochar (BC) (PEG-nZVI@BC) was prepared to remedy Cr(VI) with high efficiency. The morphology, functional groups, and crystalline structure of PEG-nZVI@BC composites were characterized, revealing that when PEG was added, a large number of -OH functional groups were introduced, and nZVI was effectively dispersed on the BC surface with a smaller particle size. The results of Cr(VI) remediation experiments showed Cr(VI) removal rate by PEG-nZVI@BC (97.38%) was much greater than that by BC-loaded nZVI (nZVI@BC) (51.73%). The pseudo second-order and Sips isotherm models provide the best simulation for Cr(VI) removal experimental data, respectively. The main remediation mechanism of Cr(VI) was reduction and co-precipitation of Cr-containing metal deposits onto PEG-nZVI@BC. Ecotoxicity assessment revealed PEG-nZVI@BC (1.00 g/L) has little influence on rice germination and growth, but resisted the toxicity of Cr(VI) to rice. The modified Community Bureau of Reference (BCR) sequential extraction showed pyrolysis could increase the percentage of oxidizable and residual Cr and diminish the environmental risk of Cr release from post-removal composites.

Surface-Engineered Super-Paramagnetic Iron Oxide Nanoparticles For Chromium Removal.

BACKGROUND: Super-paramagnetic iron oxide nanoparticles (SPIONs) are widely used metal nanoparticles for various applications for its magnetic property and biocompatibility. In recent years, pollution of our environment especially with heavy metals in waterbodies has become a major threat and has left us very minimal sources of freshwater to drink. SPIONs or surface modified SPIONs can be used to remove these heavy metals. METHODS: SPIONs were synthesized by co-precipitation method and further coated with a biopolymer, chitosan. Chromium solution was treated with the synthesized SPIONs to study the efficiency of chromium removal by surface adsorption. Later, the adsorption was analysed by direct and indirect analysis methods using UV-VIS spectrophotometry and isotherm studies. RESULTS: Stable chitosan-coated SPIONs were synthesized and they adsorbed chromium better than the uncoated SPIONs, where it was adsorbing up to 100 ppm. Adsorption was found to be increasing with decrease in pH. CONCLUSION: The surface-modified SPIONs expressed cumulative adsorption action. Even after the adsorption studies, chitosan-coated SPIONs were possessing magnetic property. Thus, the surface-modified SPIONs can become an ideal nanotechnology tool to remove the chromium from groundwater.

Calcium alginate entrapped Eupatorium adenophorum Sprengel stems powder for chromium(VI) biosorption in aqueous mediums.

A novel biosorbent, Eupatorium adenophorum Sprengel-alginate beads was used for chromium(VI) biosorption from aqueous solutions. Biosorption process was optimized at pH 2.0, biomass concentration 1.0 g/L, contact time 60 min, and temperature 30 oC respectively. Maximum uptake capacity of Cr(VI) was calculated at 28.011 mg/g. It was found that the overall biosorption process was best described by pseudo second-order kinetics with high correlation coefficient values. Intraparticle diffusion model suggested that Cr(VI) biosorption may proceed within multiple steps. Data obtained from the batch studies confirmed well to the Langmuir, Temkin, and Hill-der Boer isotherm models. Scatchard plot analysis further supported the mono-layer biosorption of Cr(VI) ions on Eupatorium adenophorum Sprengel-alginate beads as described by Langmuir isotherm model. Numerical values of E obtained from Dubinin-Radushkevich isotherm model identified the physisorption as predominant mechanism for Cr(VI) biosorption. The negative values of ΔGo confirmed the spontaneous and feasibility nature, whereas positive value of ΔHo showed the endothermic nature of biosorption process. Positive value of ΔSo indicated an increase in the randomness at the solid/solution interface during the biosorption process. The endothermic nature of Cr(VI) biosorption was also described by Temkin isotherm model. The results indicated that Cr(VI) biosorption was not significantly affected by the presence of co-ions at lower concentrations. Desorption of Cr(VI) ions from metal-loaded Eupatorium adenophorum-alginate beads was observed at 92.091% with 0.5 M HNO3 solution in solid to liquid ratio of 1.0 g/L.