Cadmium and nickel uptake by tomato and spinach seedlings: plant or transport control?

2012 ◽  
Vol 9 (1) ◽  
pp. 48 ◽  
Author(s):  
Fien Degryse ◽  
Erik Smolders

Environmental contextUptake of metal ions by plants is often predicted with equilibrium models, which assume that the rate limiting step is trans-membrane uptake of the metal in the roots rather than the transport of the metal ion towards the site of uptake. Evidence is given that uptake of cadmium by plants is under strong transport control at environmentally relevant concentrations, whereas nickel uptake borders between transport and plant control. This explains the lack of ion competition effects for Cd uptake, whereas both proton and Mg ions were found to compete with Ni uptake. AbstractEquilibrium models for metal uptake by biota assume that the uptake is rate limited by the internalisation of the metal across the cell membrane (plant control). However, evidence has been found that Cd uptake by plants is controlled by the diffusive transport of the free ion to the root at low Cd2+ activities. In this study, the uptake of Cd and Ni by tomato and spinach in nutrient solution was compared to assess whether Ni uptake is under plant or transport control. The diffusive gradient in thin films (DGT) technique was used to measure the maximal diffusive flux. In unbuffered solutions, the uptake flux of Ni was approximately three-fold smaller than that of Cd at free ion concentrations below 1 µM. Stirring the solution increased the uptake of Cd, but not that of Ni at low free ion concentration. The presence of DGT-labile complexes increased the uptake of Cd, but not that of Ni, except at high pH (pH 7). Increasing the solution pH increased Cd uptake only when solution Cd2+ activities were strongly buffered. Overall, the results indicated that the Cd uptake was strongly diffusion limited and that uptake is likely to be under transport control in natural environments. Uptake of nickel, on the other hand, appears to be at the border between plant and transport control. This finding has practical applications, e.g. competition effects at the root have little effect on Cd uptake and chelator-assisted phytoextraction is expected to have less effect for Ni than for Cd.

2016 ◽  
Vol 13 (3) ◽  
pp. 478 ◽  
Author(s):  
Sébastien Leguay ◽  
Peter G. C. Campbell ◽  
Claude Fortin

Environmental context The lanthanides are a group of heavy elements (from lanthanum to lutetium) increasingly used in many electronic consumer products and little is known about their environmental mobility and toxicity. In natural systems, these elements will bind to natural organic matter but metal toxicity is usually defined by the free metal ion concentration. Here, we propose a method based on sample equilibration with an ion-exchange resin to measure the free lanthanide ion concentration in the presence of natural organic matter. Abstract An ion-exchange technique that employs a polystyrene sulphonate ion-exchange resin was developed for determining environmentally relevant free-ion concentrations of Ce, Eu, La and Nd. Owing to the high affinity of rare earth elements (REE) for the selected resin, this method requires the addition of an inert salt to increase the concentration of the counter-ions (i.e. cations that are exchanged with REE bound to the resin). The use of a batch equilibration approach to calibrate the resin allowed the implementation of the ion-exchange technique at reasonably low ionic strength (I = 0.1M). Several ligands were used to test the selectivity of the method, which proved to be highly selective for the free metal ion in presence of the tested cationic and anionic complexes (REE–nitrate, REE–malic acid and REE–nitrilotriacetic acid systems) and operational for very low proportions of REE3+, owing to the strong REE–resin interactions. The ion-exchange technique was also implemented to determine [Eu]inorg in the presence of natural humic matter (Suwannee River Humic Acid) and the results were compared with those obtained using equilibrium dialysis and those calculated with chemical equilibrium models. At pH 4.00, the measured [Eu]inorg values were in fairly good agreement with those predicted with the Windermere Humic Aqueous Model and Stockholm Humic Model, whereas the Non-Ideal Competitive Absorption model appeared to underestimate the [Eu]inorg. However, the inorganic europium concentrations were strongly underestimated (4 < [Eu]inorg, IET/[Eu]inorg, calc < 18) with the three prediction models at higher pH (5.3 and 6.2).


2021 ◽  
Author(s):  
C Donga ◽  
S Mishra ◽  
A Aziz ◽  
L Ndlovu ◽  
A Kuvarega ◽  
...  

Abstract (3-aminopropyl) triethoxysilane (APTES) modified magnetic graphene oxide was synthesized and applied in the adsorption of three heavy metals, Pb(II), Cd(II) and Ni(II) from aqueous solution. An approach to prepare magnetic GO was adopted by using (3-aminopropyl) triethoxysilane (APTES) as a functionalizing agent on magnetic nanosilica coupled with GO to form the Fe3O4@SiO2-NH2/GO nanocomposite. FT-IR, XRD, BET, UV, VSM, SAXS, SEM and TEM were used to characterize the synthesized nanoadsorbents. Batch adsorption studies were conducted to investigate the effect of solution pH, initial metal ion concentration, adsorbent dosage and contact time. The maximum equilibrium time was found to be 30 min for Pb(II), Cd(II) and 60 min for Ni(II). The kinetics studies showed that the adsorption of Pb(II), Cd(II) and Ni(II) onto Fe3O4@SiO2-NH2/GO followed the pseudo-second-order kinetics. All the adsorption equilibrium data were well fitted to Langmuir isotherm model and maximum monolayer adsorption capacity for Pb(II), Cd(II) and Ni(II) were 13.46, 18.58 and 13.52 mgg-1, respectively. The Fe3O4@SiO2-NH2/GO adsorbents were reused for at least 7 cycles without the leaching of mineral core, showing the enhanced stability and potential application of Fe3O4@SiO2-NH2/GO adsorbents in water/wastewater treatment.


Water ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 2325 ◽  
Author(s):  
Mubeen Isam ◽  
Lavania Baloo ◽  
Shamsul Rahman Mohamed Kutty ◽  
Saba Yavari

The removal of Pb (II) and Cu (II) ions by using marine red macroalgae (Gracilaria changii) as a biosorbent material was evaluated through the batch equilibrium technique. The effect of solution pH on the removal of metal ions was investigated within the range of 2–7. The response surface methodology (RSM) technique involving central composite design (CCD) was utilised to optimise the three main sorption parameters, namely initial metal ion concentration, contact time, and biosorbent dosage, to achieve maximum ion removal. The models’ adequacy of response was verified by ANOVA. The optimum conditions for removal of Pb (II) and Cu (II) were as follows: pH values of 4.5 and 5, initial concentrations of 40 mg/L, contact times of 115 and 45 min, and biosorbent dosage of 1 g/L, at which the maximum removal percentages were 96.3% and 44.77%, respectively. The results of the adsorption isotherm study showed that the data fitted well with the Langmuir’s model for Pb (II) and Cu (II). The results of the adsorption kinetic study showed that the data fitted well with the pseudo-second order model for Pb (II) and Cu (II). In conclusion, red alga biomass exhibits great potential as an efficient low-cost sorbent for removal of metal ions.


2020 ◽  
Vol 32 (4) ◽  
pp. 876-880
Author(s):  
Maninder Singh ◽  
D. P. Tiwari ◽  
Mamta Bhagat

The indiscriminate discharge of heavy metals into water and soil from anthropogenic practices is becoming prominent threat to the environment. Heavy metals like chromium, cadmium, lead, arsenic, nickel etc. are heavily toxic and carcinogenic in nature. This study emphasizes the adequacy of activated water chest nut (Trapa natans) peel powder as a new adsorbent material for removal of chromium(VI) metal ions. Adsorption experiments were performed in batch process. Various process parameters like contact time, temperature, solution pH, dose of adsorbent, metal ion concentration etc. were optimized. The physico-chemical properties of adsorbent material were characterized by FTIR and XRD. The morphology, topology of adsorbent surface was characterized by scanning electron microscopy (SEM) and Brunauer, Emmett and Teller (BET) which revealed a highly porous structure and available specific surface area. The adsorption capacity (maximum) was counted as 59.17 mg/g and specific surface area was found 23.467 m2/g at a pH 7. The adsorption process for Cr(VI) ions was in a good agreement with Langmuir isotherm. The process also followed pseudo second order kinetics. The obtained result shows that activated water chest nut (Trapa natans) peel powder (AWCPP) can be a hopeful low-cost and eco-friendly bio-adsorbent for removal of Cr(VI) metal ions and also better adsorbent than other various reported adsorbents.


2021 ◽  
Vol 25 (1) ◽  
pp. 853-864
Author(s):  
Gideon Masedi Nii Ayi Lomoko ◽  
Dainius Paliulis ◽  
Karlis Valters

Abstract The discharge of wastewater containing heavy metals into waterbodies is a major environmental issue that can influence the quality of the water supply; therefore, it is important to remove the pollutants dangerous to living organisms. The adsorption of copper (II) ions on modified wheat bran was investigated with respect to initial solution pH (2.0-7.0), contact time (5–120 min), adsorbent mass (0.5 g and 1.0 g), and initial metal ion concentration (2.0–20 mg/L). The optimum adsorption conditions were found to be at pH 5.0 and a contact time of 60 min with an adsorbent mass of 1.0 g where the maximum efficiency was recorded as 84.5 %. The adsorption uptake (in mg/g) of copper (II) ions slowly reached equilibrium in around 30 min and this amount was 0.30 mg/g using an adsorbent mass of 0.5 g. The adsorption uptake of copper (II) ions decreased with increasing mass of adsorbent and the adsorption efficiency (in %) increased with increasing mass of adsorbent. The experimental results were described using the Langmuir and Freundlich models, with the Langmuir model fitting better than the Freundlich model. The maximum modelled adsorption capacity was 4.24 mg/g and the modelled specific surface area of modified wheat bran was 6.36 m2. It was observed that the adsorption of copper (II) ions on modified wheat bran is efficient and suitable, therefore modified wheat bran is a relatively good adsorbent for the removal of copper (II) ions from polluted water compared to other agricultural adsorbents.


Clay Minerals ◽  
2013 ◽  
Vol 48 (5) ◽  
pp. 771-787 ◽  
Author(s):  
A. Bourliva ◽  
K. Michailidis ◽  
C. Sikalidis ◽  
A. Filippidis ◽  
M. Betsiou

AbstractThree bentonite samples (B1, B2, B3) from Milos Island, Greece, were investigated by XRD, AAS, DTA-TG, FTIR and specific surface area measurement techniques. A laboratory batch study has been performed to investigate the adsorption characteristics of lead ions (Pb2+) onto natural bentonite samples. The effect of various physicochemical factors that influence adsorption, such as solution pH (2–6), adsorbent dosage (1–10 g L–1), contact time (20–360 min), and initial metal ion concentration (5–150 mg L–1) was studied. A number of available models like the Lagergren pseudo first-order kinetic model, the pseudo second-order kinetic model and intra-particle diffusion were utilized to evaluate the adsorption kinetics. The adsorption of Pb2+ was modelled with the Langmuir, Freundlich and D-R isotherms. The maximum Pb2+ adsorption capacities for B1, B2 and B3 were 85.47 mg g–1, 73.42 mg g–1 and 48.66 mg g–1, respectively.


Author(s):  
Stephanie B. Tumampos ◽  
Benny Marie B. Ensano ◽  
Sheila Mae B. Pingul-Ong ◽  
Dennis C. Ong ◽  
Chi-Chuan Kan ◽  
...  

The ubiquitous occurrence of heavy metals in the aquatic environment remains a serious environmental and health issue. The recovery of metals from wastes and their use for the abatement of toxic heavy metals from contaminated waters appear to be practical approaches. In this study, manganese was recovered from groundwater treatment sludge via reductive acid leaching and converted into spherical aggregates of high-purity MnO2. The as-synthesized MnO2 was used to adsorb Cu(II) and Pb(II) from single-component metal solutions. High metal uptake of 119.90 mg g−1 for Cu(II) and 177.89 mg g−1 for Pb(II) was attained at initial metal ion concentration, solution pH, and temperature of 200 mg L−1, 5.0, and 25 °C, respectively. The Langmuir isotherm model best described the equilibrium metal adsorption, indicating that a single layer of Cu(II) or Pb(II) was formed on the surface of the MnO2 adsorbent. The pseudo-second-order model adequately fit the Cu(II) and Pb(II) kinetic data confirming that chemisorption was the rate-limiting step. Thermodynamic studies revealed that Cu(II) or Pb(II) adsorption onto MnO2 was spontaneous, endothermic, and had increased randomness. Overall, the use of MnO2 prepared from groundwater treatment sludge is an effective, economical, and environmentally sustainable substitute to expensive reagents for toxic metal ion removal from water matrices.


2021 ◽  
Vol 2021 ◽  
pp. 1-13
Author(s):  
Wedad A. Al-Onazi ◽  
Mohamed H.H. Ali ◽  
Tahani Al-Garni

Some agricultural byproducts are useful for solving wastewater pollution problems. These byproducts are of low cost and are effective and ecofriendly. The study aim was to investigate the possibility of using pomegranate peel (PP) and date pit (DP) activated carbon (PPAC and DPAC, respectively) as sorbents to remove Cd(II) and Pb(II) from aqueous solutions. Agricultural wastes of DPs and PPs were subjected to carbonization and chemical activation with H3PO4 (60%) and ZnCl2 and used as adsorbents to remove Cd(II) and Pb(II) from their aqueous solutions. The physical characterizations of PPAC and DPAC, including determination of surface area, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and Fourier-transform infrared spectroscopy, were performed. The following factors affected adsorption: solution pH, adsorbent dosage, initial metal ion concentration, and contact time. These factors were studied to identify the optimal adsorption conditions. The results showed that the maximum adsorptions of Cd(II) and Pb(II) were achieved at pH ranging from 6 to 6.5, 90 min contact time, and 0.5 g/L for PPAC and 1 g/L for DPAC dosage. Furthermore, the adsorption efficiencies for both Pb(II) and Cd(II) were higher for PPAC than for DPAC. However, the recorded Qmax values for PPAC were 68.6 and 53.8 mg/g for Pb(II) and Cd(II) and for DPAC were 34.18 and 32.90 mg/g for Pb(II) and Cd(II), respectively. The Langmuir isotherm model fit the adsorption data better than the Freundlich model. Kinetically, the adsorption reaction followed a pseudo-second-order reaction model, with qe ranging from 12.0 to 22.37 mg/g and an R2 value of 0.99.


2019 ◽  
Author(s):  
Chem Int

The equilibrium, kinetics, and thermodynamics of the biosorption of Pb(II), Cd(II) and Zn(II) onto groundnut (Arachis hypogaea) shell were investigated under various physicochemical parameters. Optimisation studies were carried out using batch biosorption studies. The extent of the metal ion biosorption increased with increase in solution pH, initial metal ion concentration, dosage of biosorbent and contact time but decreased with the temperature of the system. The biosorption of each of the metal ions was found to be pH-dependent. Kinetic study showed that the metal ions biosorption process followed the pseudo-second-order kinetic model. The sorption of each metal ion was analysed with Freundlich and Langmuir isotherm models, in each case, the equilibrium data were better represented by Freundlich isotherm model. Thermodynamically, parameters such as standard Gibbs free energy (ΔG˚), standard enthalpy (ΔH˚), standard entropy (ΔS˚) and the activation energy (A) were calculated. The biosorption of each metal ion was spontaneous and the order of spontaneity of the biosorption process being Cd(II) &gt; Zn(II) &gt; Pb(II). Similarly, change in entropy was observed for each and the order of disorder is Cd(II) &gt; Zn(II) &gt; Pb(II).


1970 ◽  
Vol 33 (2) ◽  
pp. 167-178
Author(s):  
Tajmeri SA Islam ◽  
Hosne Ara Begum ◽  
Mohammad Abul Hossain ◽  
Mohammad Tanvir Rahman

Batch sorption study was performed using used black tea leaves (UBTL) as a low-cost adsorbent for the removal of lead (II) from aqueous solutions. Experiments were conducted as a function of contact time, initial metal ion concentration, solution pH and temperature. The sorption of Pb(II) on used tea leaves increases with increase of initial pH of solution upto a certain limit which corresponds to the pH nearly 5. The sorption isotherms follow Langmuir equation better than Freundlich equation. Again the Langmuir equation is more applicable at higher temperatures compared to those at low temperature at all pH. The monolayer sorption capacity decreases with increase in processing temperature but the overall sorbed amount increased with the increase in temperature at all pH. The positive value of estimated heat of sorption suggests the activated sorption. A probable mechanism of the sorption of Pb(II) on used tea leaves was proposed based on the surface charge of used tea leaves and the change of charge of Pb(II) with the pH of solution. DOI: 10.3329/jbas.v33i2.4100 Journal of Bangladesh Academy of Sciences, Vol. 33, No. 2, 167-178, 2009


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