Heavy Metal Adsorption Capacity Research Articles

Modifying Natural Zeolites to Improve Heavy Metal Adsorption

Problems with increasing heavy metal contents in natural waters are becoming a global issue. At the same time, improved methods for water treatment are becoming increasingly important. In this context, natural zeolites can be used to purify polluted water. In this paper, we investigated how the adsorption capacity of natural zeolites can be improved. Natural zeolites from the Shankanay district, Almaty, Kazakhstan, were used as adsorbent material for experiments on improving the water treatment of heavy metals. We found that the adsorption capacity for heavy metals was increased greatly by thermal activation using furnace treatment. The optimal thermal activation condition was about 550 °C for a duration of 2 h. However, the improved adsorption capacity for different heavy metals varied depending on the heat treatment temperature. Adsorption by the heat-treated zeolites at a temperature of 550 °C was 87% for nickel, 99% for copper and cadmium, and 100% for lead. Adsorption by heat-treated zeolites at a temperature of 500 °C was 78% for nickel, 98% for copper, 83% for cadmium, and 88% for lead. The residual concentration of heavy metals in the filtered water did not exceed the maximum permissible concentrations for drinking purposes. In all experiments, intense adsorption took place during the first 10 min representing 35 to 61% of the metal ions in the water. Adsorption properties were verified using adsorption capacity (BET), IR spectroscopy, and scanning electron microscopy. The study shows that modified Shankanay natural zeolites have great potential as a low-cost adsorbent material for purifying water from heavy metals.

The types of microplastics, heavy metals, and adsorption environments control the microplastic adsorption capacity of heavy metals.

Anthropogenic development has released large amounts of microplastics (MPs), which are carriers of migratory heavy metals, into the environment, and heavy metal adsorption by MPs may have strong combined toxic effects on ecosystems. However, until now, a comprehensive understanding of the factors influencing these adsorption capacities of MPs has been lacking. Thus, we used 4984 experimental data points to systematically assess the factors influencing the adsorption strength of 8 types of MPs on 13 types of heavy metals. We found that (1) the types of MPs, heavy metals, and adsorption environments significantly impacted the heavy metal adsorption capacities of MPs; (2) polyvinyl alcohol (PVA) showed a higher adsorption capacity for lead (Pb) and cadmium (Cd) than did other MPs, by 2810.62mg/kg and 2732.84mg/kg, respectively; (3) the adsorption capacities of MPs for heavy metal were regulated by multiple variables, with heavy metal concentration, MP quality, solution amount, adsorption time, and pH being the most important; and (4) MPs had a higher adsorption capacity in aquatic environments (except for seawater) than which in soil environments. Overall, our study clearly showed that the types of heavy metals, adsorption environments, and MPs influenced the heavy metal adsorption capacities of MPs and may exacerbate their combined environmental toxicity, which would help better characterize the severity of MP pollution.

Multifunctional fully biobased aerogels for water remediation: Applications for dye and heavy metal adsorption and oil/water separation

Water ecosystem contamination from industrial pollutants is an emerging threat to both humans and native species, making it a point of global concern. In this work, fully biobased aerogels (FBAs) were developed by using low-cost cellulose filament (CF), chitosan (CS), citric acid (CA), and a simple and scalable approach, for water remediation applications. The FBAs displayed superior mechanical properties (up to ∼65 kPa m3 kg−1 specific Young’s modulus and ∼111 kJ/m3 energy absorption) due to CA acting as a covalent crosslinker in addition to the natural hydrogen bonding and electrostatic interactions between CF and CS. The addition of CS and CA increased the variety of functional groups (carboxylic acid, hydroxyl and amines) on the materials’ surface, resulting in super-high dye and heavy metal adsorption capacities (619 mg/g and 206 mg/g for methylene blue and copper, respectively). Further modification of FBAs with a simple approach using methyltrimethoxysilane endowed aerogel oleophilic and hydrophobic properties. The developed FBAs showed a fast performance in water and oil/organic solvents separation with more than 96% efficiency. Besides, the FBA sorbents could be regenerated and reused for multiple cycles without any significant impact on their performance. Moreover, thanks to the presence of amine groups by addition of CS, FBAs also displayed antibacterial properties by preventing the growth of Escherichia coli on their surface. This work demonstrates the preparation of FBAs from abundant, sustainable, and inexpensive natural resources for applications in wastewater purification.

Comparison of the adsorption capacity and mechanisms of mixed heavy metals in wastewater by sheep manure biochar and Robinia pseudoacacia biochar.

Under various pyrolysis temperatures, the characteristics and heavy metal adsorption capabilities of biochar obtained from sheep manure (SMB) and Robinia pseudoacacia (RPB) were studied. The results indicated that SMB had higher yields, pH values, and ash contents than RPB. SMB3 and RPB3 have more oxygen-containing functional groups, whereas SMB8 and RPB8 have higher aromaticity and polarity. The maximum adsorption capacities of SMB for Pb2+ (20.2 mg·g-1), Cu2+ (13.9 mg·g-1), Cd2+ (3.2 mg·g-1), and total heavy metals (37.3 mg·g-1) were obtained by SMB3. However, the maximum adsorption capacities of RPB for Pb2+ (7.4 mg·g-1) and Cu2+ (10.5 mg·g-1) were obtained by RPB8. Furthermore, SMB and RPB had relatively higher adsorption capacities for Pb2+ and Cu2+ than for Cd2+. The pseudo-second-order model and the Freundlich Langmuir model provided a good fit to the adsorption kinetics and isotherms, indicating that chemical adsorption was dominant in the heavy metal adsorption by SMB and RPB. According to the contribution of various mechanisms, ion exchange and mineral precipitation were the primary mechanisms responsible for RPB8, while functional group complexation was the dominant mechanism for SMB3. This study provided important information on the comprehensive recycling utilization of SMB and RPB and promoted sustainable development.

Calcium-doped magnetic humic acid nano particles for the efficient removal of heavy metals from wastewater: the role of Ca

ABSTRACT Ca doping is an effective method for improving the adsorption capacity of HA–Fe aggregates and regulating their structures. Understanding the structural characteristics of Ca–HA–Fe aggregates can help explore their microscopic adsorption effect on heavy metals. However, the heterogeneity of HA results in an incomplete understanding of the structural characteristics of the ternary system of Ca–HA–Fe aggregates and adsorption of the quaternary system of Ca–HA–Fe–Pb/Cu/Cd. In this study, interactions between Ca–HA–Fe ternary and Ca–HA–Fe–Pb/Cu/Cd quaternary systems were discussed from a molecular perspective. The structures of the basic structural units of HA were identified. Density functional theory (DFT) was employed to calculate the stable states of basic structural units of HA and Ca2+. The results showed that hydroxyl and carboxyl groups exhibited the highest capacity to bind with Ca2+. The interactions among Ca, HA, and Fe led to the formation of network aggregates. The binding energies of functional groups for heavy metals and the feasibility of ion exchange were calculated by the method of experiment and DFT. According to the contribution of functional group complexation and ion exchange, the ion exchange values for Pb2+, Cu2+, and Cd2+ were 66.71%, 62.87%, and 60.79%, respectively, which indicated that Ca2+ ion exchange showed considerable potential in enhancing the adsorption capacity of heavy metals.

Adsorption and desorption characteristics of heavy metals onto conventional and biodegradable plastics

Biodegradable plastics have been widely used to replace conventional plastics to minimize environmental impacts of plastic packaging. However, before biodegradable plastics decompose in the environment, they could pose a threat to terrestrial and aquatic creatures by acting as vectors of contaminants in the food chain. In this study, conventional plastic bags (CPBs) made of polyethylene and biodegradable plastic bags (BPBs) made of polylactic acid were examined for their heavy metal adsorption. Effects of solution pHs and temperatures on adsorption reactions were investigated. Because of a larger BET surface area, presence of oxygen-containing function groups, and smaller crystallinity, the heavy metal adsorption capacities of BPBs are significantly larger than those of CPBs. Among Cu (up to 791.48 mg⋅kg−1), Ni (up to 60.88 mg⋅kg−1), Pb (up to 1414.58 mg⋅kg−1), and Zn (up to 295.17 mg⋅kg−1), Pb and Ni show the largest and the lowest extents of adsorption onto the plastic bags, respectively. In the different waterbodies in nature, Pb adsorption on the CPBs and the BPBs were 318.09–379.91 and 528.41–764.22 mg⋅kg−1, respectively. Consequently, Pb was selected as the target contaminant in the desorption experiments. After Pb was adsorbed onto the CPBs and the BPBs, Pb could be completely desorbed and released into simulated digestive systems in 10 h. In conclusion, BPBs could be potential vectors of heavy metals, and their suitability as a substitute for CPBs must be thoroughly investigated and confirmed.

Delamination of multilayer Ti3C2Tx MXene alters its adsorpiton and reduction of heavy metals in water

MXenes are considered as an emerging class of two-dimensional (2D) adsorbent for various environmental applications. In this work, two different morphologies of Ti3C2Tx MXene (multilayer (ML-Ti3C2Tx) and delaminated titanium carbide (DL-Ti3C2Tx)) were prepared through mild in situ HF etching and further delamination. The structural differences between the two were explored with a focus on their effects on the performance and mechanism of removing heavy metals from water. In comparison to ML-Ti3C2Tx, DL-Ti3C2Tx had more oxygen-containing functional groups, higher specific surface area (19.713 vs. 8.243 m2/g), larger pore volume (0.135 vs. 0.040 cm3/g), higher maximum Pb(II) adsorption capacity (77.0 vs. 56.68 mg/g), but lower maximum Cu(II) adsorption capacity (23.08 vs. 55.46 mg/g). Further investigation revealed that the removal of Pb(II) by the MXenes was mainly controlled through electrostatic attraction and surface complexation mechanisms, while Cu(II) was removed mainly through surface reduction by Ti-related groups. Because delamination of ML-Ti3C2Tx increased the surface area and surface functional groups, DL-Ti3C2Tx became a better sorbent for Pb(II) in water. During sonication, however, delamination inevitably led to partial oxidation of Ti3C2Tx nanosheets and thus weakened the reducing ability of DL-Ti3C2Tx for Cu(II) in water. Nevertheless, both ML- and DL-Ti3C2Tx not only exhibited excellent heavy metal adsorption capacity under different solution conditions, but also showed good reusability. Findings of this study indicate that Ti3C2Tx MXenes are promising adsorbents for treating heavy metal pollutants in water.

Effects of winter warming on the migration characteristics and pollution risk assessment of Zn, Cu, and Pb in the snow-soil continuum in seasonal snow cover area

The response of snow to climate warming is extremely sensitive. Climate warming will affect the melting rate of snow and its adsorption capacity for heavy metals, thereby affecting soil heavy metal content and pollution risk. This study regards snow and soil as a continuum, and two different warming treatments and one control treatment were set up with infrared radiometer to simulate the changing characteristics of this process under the background of future climate warming. In controlled experiments, the content of Zn, Cu and Pb in snow decreased significantly due to climate warming. Compared with the warming treatments, the concentrations of Zn, Cu, and Pb in the control treatment were increased by 6μg L−1, 4.9μg L−1, and 1μg L−1 and 8.3μg L−1, 1.75μg L−1, and 2.85μg L−1, respectively. The positive response of snow to climate warming directly affected the spatio-temporal distribution pattern of Zn, Cu, and Pb in soil, as a result, the Igeo of soil Zn increased by 0.221 and 0.165, the Igeo of soil Cu decreased by 0.076 and 0.080, and the Igeo of soil Pb decreased by 0.018 and 0.073, respectively. Thus, the living environment of soil microorganisms was changed, and the ecological environment of soil was significantly affected. Our results highlighted the importance of snow cover in assessing the risk of soil heavy metal pollution in the context of future warming, meanwhile, the results had important reference value for pollution prevention and sustainable development of farmland ecosystem in seasonal snow cover area.

High-efficiency electrochemical removal of Cd(II) from wastewater using birnessite-biochar composites: Performance and mechanism.

Birnessite has been widely used for electrochemical removal of heavy metals due to its high pseudocapacitance. Incorporation of carbon-based materials into birnessite can enhance its conductivity and stability, and synergistically improve the electrochemical adsorption capacity due to the double-layer capacitor reaction derived from carbon-based materials. In this study, biochar was successfully incorporated with birnessite at various ratios to synthesize composites (BC-Mn) for effective electrochemical removal of cadmium (Cd(II)) from water. The effects of cell voltage, initial pH, and recycling performance of BC-Mn were evaluated. As a result, the electrosorption capacity of BC-Mn for Cd(II) exhibited gradual increases with increasing birnessite content and reached equilibrium at a Mn content of 20% (BC-Mn20). The Cd(II) adsorption capacity of BC-Mn20 rose at higher cell voltage, and reached the maximum at 1.2V. At pH 3.0-6.0, the electrosorption capacity initially rose until pH 5.0 and then approached equilibrium with a further increase in pH value. The Cd(II) electrochemical adsorption capacity of BC-Mn20 in the solution could reach 104.5mgg-1 at pH 5.0 for 8h at 1.2V. Moreover, BC-Mn20 exhibited excellent reusability with a stability of 95.4% (99.7mgg-1) after five cycles of reuse. Due to its superior heavy metal adsorption capacity and reusability, BC-Mn20 may have a promising prospect in the remediation of heavy metal polluted water.

Feasible synthesis of magnetic zeolite from red mud and coal gangue: Preparation, transformation and application

A feasible synthesis of magnetic zeolite from the mixture of industrial solid wastes (red mud and coal gangue) was proposed. The preparation conditions, formation mechanism and adsorption performance of magnetic zeolite were investigated. Magnetic zeolite with uniform distribution of zeolite and magnetite could be successfully synthesized at the alkali reducing calcination conditions of n(Na:Al:Si) = 3.6:1:1, 600 °C, 1.5 h and the hydrothermal conditions of n(Na:H2O) = 2.8:1, 90 °C, 9 h. During this process, aluminosilicates in the mixture of red mud and coal gangue could be transformed into sodium-containing phases and zeolite A in turn; meanwhile, hematite in red mud could be reduced by carbon in coal gangue to transform into magnetite. The prepared magnetic zeolite showed excellent adsorption capacity and reusability for heavy metals. The maximum adsorption capacity for Cu2+, Cd2+ and Pb2+ reached 76.2, 92.2 and 178.4 mg/g, respectively, which could be attributed to the different ionic radius of heavy metals.

Competitive adsorption of heavy metals between Ca–P and Mg–P products from wastewater during struvite crystallization

Wastewater usually contains high concentration of calcium (Ca), posing a competitive reaction with magnesium (Mg) on phosphorus (P) recovery during the struvite crystallization. The differences in the adsorption of heavy metals by Ca–P and Mg–P (struvite) generated are still unclear. Herein, we analyzed the residues of four kinds of common heavy metals (Cu, Zn, Cd, Pb) in Ca–P and Mg–P (struvite) under varying conditions (solution pH, N/P ratio, Mg/Ca ratio) in the swine wastewater and explored their possible competitive adsorption mechanisms. The experiments using synthetic wastewater and real wastewater have similar experimental patterns. However, under the same conditions, the metal (Pb) content of struvite recovered from the synthetic wastewater (16.58 mg/g) was higher than that of the real wastewater (11.02 mg/g), as predicted by the Box-Behnken Design of Response Surface Methodology (BBD-RSM). The results demonstrated that Cu was the least abundant in the precipitates compared to Zn, Cd, and Pb of almost all experimental groups with an N/P ratio greater than or equal to 10. The fact might be mainly attributed to the its stronger binding capacity of Cu ion with NH3 and other ligands. Compared with struvite, the Ca–P product had a higher adsorption capacity for heavy metals and a lower P recovery rate. In addition, the higher solution pH and N/P ratio were favorable to obtain qualified struvite with lower heavy metal content. It can be applied to reduce the incorporation of heavy metals by modulating pH and N/P ratio through RSM, which is suitable for different Mg/Ca ratios. It is anticipated that the results obtained would offer support for the safe utility of struvite from wastewater containing Ca and heavy metals.

Adsorption of heavy metals from mine wastewater using amino-acid modified Montmorillonite

This study was conducted to identify the ability of a modern developed amino-acid modified montmorillonite clay (AA-Mont) to adsorb Cu2+, Pb2+ and Ni2+ cations from a multi-aqueous wastewater. This experimental was conducted to identify the potential of clay-based adsorbents to remediate pollutants from the PRA river basin. Experimental wastewater was prepared using a range of the lowest and highest recorded upstream and downstream heavy metal concentrations of u2+(10.84 mg/L-108.48 mg/g), Ni2+(7.99 mg/g–79.92 mg/g), and Pb2+(33.538 mg/L—335.38 mg/L). The variants of the designed clay-based adsorbents were L-Cysteine montmorillonites (Cys-Mont), Glycine montmorillonite (Gly-Mont), and L-lysine Montmorillonites (Lys-Mont) prepared at pH 4, 5, and 6 respectively. The experimental conditions were; Adsorbent dosages range = 25 mg–400 mg, pH = 6.0, Contact time = 24 hrs, Temperature = 25°C and Shaker speed = 180 rmp. After the adsorption experiments, it was identified that the maximum average removal efficiency obtained for Cu2+, Ni2+, and Pb2+ were all attained at adsorbent dosage 400 mg/L and in the order Lys-Mont (99.82%)>Cys-Mont (99.28%)>Gly-Mont (95.8%). Thus, the modified Lys-Mont clay exhibited the highest heavy metal adsorption capacity amongst the above three studied. The highest and lowest adsorbed metal pollutants amounts recorded for Lys-Mont were Cu2+ (86.49 and 8.65) mg/g, Ni2+ (44.51 and 5.99) mg/g, and Pb2+ (267.85 and 26.67) mg/g respectively. The number of metal ions adsorbed per unit mass for each metal cation tested decreased with increasing adsorbent dosage. The general order of selectivity documented for all the AA-Monts in this study was Pb>Cu>Ni which is similar to the levels in the prepared wastewater solution (Pb>Cu>Ni). The findings of this study have shown that heavy metal polluted river basins can remediated given the right conditions of temperature, adsorbent dosage, pH and agitation speed.

Modified Shrimp-Based Chitosan as an Emerging Adsorbent Removing Heavy Metals (Chromium, Nickel, Arsenic, and Cobalt) from Polluted Water

Water quality is under constant threat worldwide due to the discharge of heavy metals into the water from industrial waste. In this report, we introduce a potential candidate, chitosan, extracted and isolated from shrimp shells, that can adsorb heavy metals from polluted water. The waste shrimp shell chitosan was characterized via Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS). The adsorption capacity of heavy metals on the modified shrimp shell was measured using an inductively coupled plasma mass spectrometry before and after adsorption. The highest adsorption of arsenic, nickel, and cobalt was 98.50, 74.50, and 47.82%, respectively, at neutral pH, whereas the highest adsorption of chromium was 97.40% at pH 3. Correspondingly, the maximum adsorption capacities of MSS for As, Cr, Ni, and Co were observed to be 15.92, 20.37, 7.00, and 6.27 mg/g, respectively. The application of Langmuir and Freundlich isotherm models revealed that the adsorption processes for the heavy metals were statistically significant (r2 > 0.98). The kinetic studies of metal adsorption, using modified shrimp shell, were well explained by the pseudo-second-order kinetic model with linear coefficients (r2) of >0.97. The presence of a greater number of functional groups on the adsorbent, such as N–H coupled with H–O, –COO−, C–H, N–N, and C–O–C, was confirmed by FTIR analyses. Furthermore, SEM-EDX analysis detected the presence of elements on the surface of modified shrimp shell chitosan. This noteworthy adsorption capacity suggests that MSS could serve as a promising, eco-friendly, and low-cost adsorbent for removing toxic heavy metals including Cr, Ni, As, and Co and can be used in many broad-scale applications to clean wastewater.

Waste to resource: Utilization of waste bagasse as an alternative adsorbent to remove heavy metals from wastewaters in sub-Saharan Africa: A review

AbstractHeavy metals pollution of both surface and groundwater sources of sub-Saharan Africa is alarmingly increased due to unplanned urban populations. Inadequate policies for water management, political commitment, and financial resources forced 65% of rural communities of sub-Saharan Africa to live in economic water stress areas. Sugarcane bagasse (SCB) shows high heavy metals (HMs) adsorption capacity (20–700 mg/g) through chemical entrapments to carbon-oxygen containing functional group and interior pore filling of porous surface. Various modifications like a physical/thermal, chemical, and composite form of bagasse show better adsorption performance for HMs removal. Kinetic and isotherm studies of HMs adsorption equilibrium data over SCB show that both Langmuir and Freundlich adsorption isotherms (cooperative adsorption) as the main adsorption mechanism. In addition, SCB shows potential bio-adsorbent properties for the selective adsorption of target HMs based on their physicochemical properties and shows good repeatability in acid environments. It is believed that information on this review will shed light on the current and future prospects of raw and modified SCB for HMs adsorption removal capacity. Sugarcane bagasse shows a remarkable selectivity for HMs adsorption removals based on their physicochemical properties and shows good potential capability for future utilizations in real wastewaters of developing countries.

Runoff regulation and nitrogen and phosphorus removal performance of a bioretention substrate with HDTMA-modified zeolite

As a commonly used material in bioretention substrates, natural zeolite (NZ) provides decent adsorption capacity for cation pollutants and heavy metals, but limited ability to remove anion pollutants. Hexadecyltrimethylammonium bromide (HDTMA)-modified zeolite (MZ) was used as the bioretention substrate material. The performance of the media including runoff reduction, nitrate nitrogen (NO3−-N) removal, ammonium nitrogen (NH4+-N) removal, and total phosphorus (TP) removal was assessed by the column experiment. The effects of different levels of modification, ratio of zeolite in the substrate, and rainfall intensity on media performance were investigated. The results indicate that HDTMA-modified zeolite significantly improves the NO3−-N (up to 38.2 times of NZ) and TP (up to17.5 times of NZ) removal rate of media and slightly increases the NH4+-N (up to 1.5 times of NZ) purification performance of the substrate. Compared with the media with NZ, decline on both runoff volume reduction (maximum decline up to 32.9%) and flow rate reduction (maximum decline up to 29.9%) of the media with MZ were observed. Based on multiple regression analysis, quantitative relationship models between influencing factors and response variables were established (R2 > 0.793), the level of the effect of influencing factors on response variables was investigated, and the interactions between influencing factors were explored. The main effect analysis found that the degree of modification affects NO3−-N and TP removal rate of the substrate the most, and when the amount of HDTMA molecules loaded on the zeolite surface exceeds 0.09meq/g, the modification can no longer improve NO3−-N removal efficiency.

Biomass inherent metal interfere carbothermal reduction modification of biochar for Cd immobilization

Metal salt laden are frequently used to enhance the heavy metal adsorption capacity of biochar. The present study indicates that CaS loading biochar can be modified from the carbothermal reduction reaction between CaSO3 (modification agent) and carbon matrix. The CaS transformation ratio as indicated by XPS spectra was significantly improved by the CaSO3 loading content. The coprecipitation reaction induced by the CaS in biochar can significantly enhance the adsorption capacity of heavy metals (Cd). And, the Cd adsorption capacity can be enhanced up to >100 mg/g and increases with increasing CaS ratio in the biochar. In addition, the adsorption process was rapid and could be balanced within several minutes (~ 5 min). Furthermore, the interaction reaction between the modification agent and the inherent metal in the biomass was examined in the biochar pyrolysis preparation process. Interestingly, MgCl2 inherent metal salt can combine with the original CaSO3 to produce a new mineral, resulting in a decrease in CaS. However, KCl, a more thermally stable biomass-derived metal salt, exhibited a weak combination ability with the modification agent. Accordingly, this type of secondary reaction reduces the Cd adsorption capacity owing to the decrease in the number of adsorption sites (CaS).

Study on Adsorption of Heavy Metals Cu and Zn by Microplastics Under Different Aged Factors

Microplastics are widely distributed in a variety of environments, absorbing heavy metals in the environment while aging due to various environmental factors. In this paper, the effects of different aging factors (pH, DOM, and H2O2) on the adsorption capacity of heavy metals Cu and Zn on polyethylene microplastics (PE-MPs) were investigated, and the changes in physical and chemical properties of PE microplastics were analyzed. The results demonstrate that H2O2 aging bears the greatest effect on the adsorption effect of PE microplastics, dissolved organic matter (DOM) aging has the least effect on the adsorption effect of PE microplastics, and the adsorption effect of microplastics aged with pH=9 is stronger than that aged with pH=4; the adsorption kinetics model of microplastics fitted to the pseudo-second-order kinetic model, and the thermodynamic model fitted to Langmuir model; aging mainly changed the surface structure of microplastics, increased the Zeta potential of microplastics, introduced more oxygen-containing functional groups, and finally affected the ability of microplastics to adsorb heavy metals. The research provides data reference for understanding the influence of different aging on the adsorption capacity of heavy metals in microplastics.

Adsorption of Heavy Metals on Bentonitic Soil for Use in Landfill Liners

Hazardous heavy metal ions such as copper, zinc, nickel, chromium, cadmium, and lead engender a potential risk to human health. Among the processes involved in the retention of these contaminants, adsorption is advantageous for removing toxic metals because of its environmentally friendly aspect, efficiency, and low-cost operation. Information on the adsorption of heavy metals in soils from the semiarid region of northeastern Brazil is still scarce. In this study, the adsorption of heavy metals (Cd, Cu, Zn, Ni, and Pb) by a semiarid Brazilian bentonitic soil is investigated. This soil has been used as a bottom liner in an experimental municipal solid waste (MSW) cell located in Campina Grande, State of Paraíba, Brazil. The experimental cell consists of a landfill unit on an experimental scale, with the same constructive elements of a sanitary landfill. Disturbed and undisturbed samples of the investigated soil were collected at a quarry in the rural zone of Boa Vista (state of Paraiba, Northeast Brazil). Sorption attributes were determined via batch tests with a soil-solution ratio of 1 : 12.5 (4 g of dry soil to 50 mL of solution). Linear, Freundlich, and Langmuir isotherms were fitted to the experimental data, using as fitting parameters Pearson correlation coefficient ([Formula: see text]) and [Formula: see text] value with a significance level [Formula: see text]. The ascending order of maximum adsorption capacity for heavy metals followed the series Ni < Cr < Zn < Cd < Cu < Pb. The maximum adsorbent capacities obtained were similar to those of other Brazilian soils and other adsorbents. Therefore, the studied soil has a high potential to be used in the retention of heavy metals.

Gradient heating induced better balance among water transportation, salt resistance and heat supply in a high performance multi-functional solar-thermal desalination device.

Solar-driven desalination (SDD) is a promising technology for addressing water scarcity. However, how to overcome the trade-off between water transportation and heat supply of the evaporator to achieve a high evaporation rate and good salt tolerance simultaneously remains a challenge. Here, a novel all-in-one multi-functional SDD evaporator undergoing gradient heating is used. This evaporator incorporates a hydrophilic PDA (polydopamine)@CNT(carbon nanotube)/PVA (polyvinyl alcohol) aerogel with vertically aligned structures as the water evaporation layer, enabling rapid water transportation. Surrounding the evaporation layer, there is a photothermal hydrophobic CCP (cotton/CNT/polydimethylsiloxane) film that serves as the heating layer, enhancing the heat supply to the evaporation layer. This innovative design strikes a favorable balance between water transportation and heat supply, facilitating high evaporation rates and good salt tolerance simultaneously, while also maximizing electricity generation. Due to the wettability difference between the evaporation layer (PVA aerogel) and heating layer (CCP film), a record stable temperature gradient of nearly 70 °C was formed between the CCP film and the PVA aerogel under 1 sun irradiation, so that heat on the high-temperature CCP film was continuously transferred to the low-temperature aerogel through its thermal conductive network, leading to a high evaporation rate of 6.96 kg m-2 h-1 under 1 sun irradiation in 5.0 wt% sodium chloride (NaCl) brine (higher than the world average seawater salinity (3.5 wt%)). Meanwhile, high flux directional flow of brine generated 130 mV stable voltage and 120 μA circuit current. Furthermore, the evaporator illustrates good stability for consecutive 7 days of testing and shows industry-leading comprehensive performance of SDD in actual use. More importantly, it was tested in real Bohai seawater under weak natural light, and fresh water generated can meet the recommended daily intake of water for 2.6 households and the simultaneously generated voltage reaches above 60 mV. In addition, the evaporator exhibits good adsorption capacity for heavy metals and dye molecules. This simple and universal solar evaporation structure is suitable for the assembly of gradient thermal structures for most solar thermal materials reported in the literature, which provides a new route for maximizing the use of solar energy for freshwater and electricity generation.

Efficient removal of heavy metals by endophytic bacteria Staphylococcus succinus H3.

Heavy metal pollution is a serious and difficult environmental problem. With increasing heavy metal content in industrial wastewater, an environmentally friendly and efficient treatment method must be identified. Considering the ability of endophytic bacteria to adsorb metal ions, this paper explored the heavy metal resistance, adsorption, and adsorption mechanisms and performance of S. succinus H3, an endophytic bacterium. S. succinus H3 exhibited metal resistance at 4 mM Cu2+ and 5 mM Mg2+. The adsorption rate of Cu2+ and Mg2+ ions by the live/dead strain was approximately 70%, and the adsorption capacity was positively correlated with the metal ion concentration. The kinetics and isothermal models were used to study the process of S. succinus H3 adsorption on Cu2+. It exhibits a good correlation with the Freundlich isothermal model. The N-H group, protein C=O group, polysaccharide C-O group, O-H group and some lipids are the main functional groups in the cell wall. S. succinus H3 may bond with the amine group to adsorb Mg2+ through complexation/coordination and may form a copper complex after adsorbing Cu2+. S. succinus H3 has a live adsorption rate of 15% in eight mixed metal ion systems at a 50 mg/L concentration. The study results can lay a foundation for expanding the bacterial resource pool of pollutant treatment and improving the efficiency for sewage treatment. The high heavy metal adsorption capacity of microorganisms has a decisive role in industrial wastewater treatment by microorganisms. Such microorganisms with high metal resistance and adsorption capacity to heavy metals can thrive in industrial wastewater, remove heavy metals efficiently, and greatly improve the efficiency of wastewater treatment. The study results can lay a theoretical foundation for the use of S. succinus H3 to biologically treat heavy metal wastewater in the future.