Metal Adsorption Capacity Research Articles

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.

A Study on the Impermeability of Nanodispersible Modified Bentonite Based on Colloidal Osmotic Pressure Mechanisms and the Adsorption of Harmful Substances

With the growing demands of human beings, sanitary landfill, along with the increase in landfill depth and leachate water pressure, has put forward new and higher requirements for the impermeable layer. In particular, it is required to have a certain adsorption capacity of harmful substances from the perspective of environmental protection. Hence, the impermeability of polymer bentonite–sand mixtures (PBTS) at different water pressure and the adsorption properties of polymer bentonite (PBT) on contaminants were investigated through the modification of PBT using betaine compounded with sodium polyacrylate (SPA). It was found that the composite modification of betaine and SPA could reduce the average particle size of PBT dispersed in water (reduced to 106 nm from 201 nm) and enhance the swelling properties. As the content of SPA increased, the hydraulic conductivity of PBTS system decreases and the permeability resistance improves, while the resistance to external water pressure increases. It is proposed a concept of the potential of osmotic pressure in a constrained space to explain the impermeability mechanism of PBTS. The potential of osmotic pressure obtained by linear extrapolation of the trendline of colloidal osmotic pressure versus mass content of PBT could represent the external water pressure that the PBT resist. Additionally, the PBT also has a high adsorption capacity for both organic pollutants and heavy metal ions. The adsorption rate of PBT was up to 99.36% for phenol; up to 99.9% for methylene blue; and 99.89%, 99.9%, and 95.7% for low concentrations of Pb2+, Cd2+, and Hg+, respectively. This work is expected to provide strong technical support for the future development in the field of impermeability and removal of hazardous substances (organic and heavy metals).

Fabrication of Novel Hemp Charcoal Nanofiber Membrane for Effectual Adsorption of Heavy Metal Ions from Wastewater

Water pollution is increasing with rapidly growing industries and world population, which is very harmful for marine life and humans as well. This research has been conducted to introduce novel material with advanced techniques for the effective removal of heavy metals from wastewater. Successful nanofiber membranes have been developed with hemp charcoal (HC) and polyacrylonitrile (PAN), which can remove heavy metals from water efficiently in less time. The nanofiber membranes showed good adsorption capacity for heavy metal ions along with good thermal and mechanical stability. Electrospun nanofibers of HC and PAN were assessed for adsorption capacity by soaking them in metallic suspensions of known concentration for a specific period of time. Nickle, cobalt, and copper metals were selected to assess the adsorption capacity of nanofibrous webs. It was observed that HC played a vital role in removing metal ions from wastewater with an excellent efficiency. The adsorption capacity for nickel, cobalt, and copper was 54 mg/g, 87 mg/g, and 96 mg/g, respectively.

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.

Removal of Heavy Metal Ions Using Pristine and Functionalized Natural Zeolites

Heavy metal ions have attracted significant concern regarding their toxicity in living organisms. Concurrently, the removal of heavy metals by the adsorption method is also under the spotlight because it is effective, less cost-demanding, and easy to operate. To date, natural zeolites become one of the most used adsorbents for it is low cost, abundant in reserve, and has high selectivity towards heavy metal. Zeolites possess negatively charged three-dimensional frameworks built by SiO4 and AlO4 tetrahedra, which are balanced by counter-cations. The cations within zeolite frameworks can be exchanged with the heavy metal cations in an aqueous environment. This review comprehensively reports the adsorption capacity of heavy metal ions using pristine and modified natural zeolite. The important aspects, including the physicochemical properties of pristine and modified natural zeolites, heavy metal ion adsorption isotherms, kinetics, and thermodynamics, are discussed in detail. It is imperative to note that the physicochemical properties of natural zeolites greatly determine the adsorption capability. Furthermore, natural zeolites could be modified with various molecules such as surfactants and polymers to improve the adsorption capacity and adsorb heavy metal anions. Ultimately, this review is concluded with prospects for future improvement.

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.

Synthesis of Polyvinyl Alcohol/Coal Fly Ash Hybrid Nano-Fiber Membranes for Adsorption of Heavy Metals in Diesel Fuel.

Some studies have shown that the heavy metal emissions (HMEs) emitted from diesel engines can seriously threaten human health. HMEs are mainly related to the content of heavy metal ions in diesel fuel. Therefore, in order to reduce HMEs from diesel engines, a nano-fiber membrane filtration technology for diesel fuel was investigated. Herein, coal fly ash (CFA) from coal-fired power plants combined with polyvinyl alcohol (PVA) was successfully fabricated into nano-fibrous membranes using green electrospinning technology. In order to evaluate the adsorption properties, various hybrid membranes with different mixing ratios (PVA/CFA = 10/0, 10/1, 10/3, 10/5, and 10/7 by weight) were fabricated. The results show that eight metal ions with different concentrations are found in the diesel fuel, including Pb, Cu, Zn, Al, Fe, Cr, Ba, and Ni. All PVA/FA membranes have different adsorption capacities for metal ions, following the order: Cu > Fe > Pb > Al > Zn > Cr > Ba > Ni. In addition, the adsorption capacity of CFA3 (PVA/CFA = 10/3) is the largest. The super lipophilicity of the PVA/FA membranes also provide more adsorption sites for the contact of HMs with the membranes. The above research results provide guidance for development of ultra-fine filters in the future.

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.

Superior Heavy Metal Ion Adsorption Capacity in Aqueous Solution by High-Density Thiol-Functionalized Reduced Graphene Oxides.

The preparation of mercapto-reduced graphene oxides (m-RGOs) via a solvothermal reaction using P4S10 as a thionating agent has demonstrated their potential as an absorbent for scavenging heavy metal ions, particularly Pb2+, from aqueous solutions due to the presence of thiol (-SH) functional groups on their surface. The structural and elemental analysis of m-RGOs was conducted using a range of techniques, including X-ray diffraction (XRD), Raman spectroscopy, optical microscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), scanning transmission electron microscopy equipped with energy-dispersive spectroscopy (STEM-EDS), and X-ray photoelectron spectroscopy (XPS). At pH 7 and 25 °C, the maximum adsorption capacity of Pb2+ ions on the surface of m-RGOs was determined to be approximately 858 mg/g. The heavy metal-S binding energies were used to determine the percent removal of the tested heavy metal ions, with Pb2+ exhibiting the highest percentage removal, followed by Hg2+ and Cd2+ ions having the lowest percent removal, and the binding energies observed were Pb-S at 346 kJ/mol, Hg-S at 217 kJ/mol, and Cd-S at 208 kJ/mol. The time-dependent removal study of Pb2+ ions also yielded promising results, with almost 98% of Pb2+ ions being removed within 30 min at pH 7 and 25 °C using a 1 ppm Pb2+ solution as the test solution. The findings of this study clearly demonstrate the potential and efficiency of thiol-functionalized carbonaceous material for the removal of environmentally harmful Pb2+ from groundwater.

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.

REVIEW OF ADSORPTION OF HEAVY METALS BY ADSORBENT MnFe2O4 – ZEOLITE IN WATER

The existence of quality water on earth is essential for life and the consumption of existing living things. The problem of water pollution is a matter of great concern in world researchers' management of water resources. Heavy metals have a toxic effect on humans and the environment. This paper reviews the characteristics and methods of synthesis of MnFe2O4 and zeolite materials as adsorbents for removing heavy metal ions in water with critical properties such as surface area, magnetic properties, and adsorption capacity. We have collected data regarding the appropriate method for synthesizing MnFe2O4 and zeolite nano adsorbents. We have accumulated much data on the properties of MnFe2O4 and zeolite materials and the optimum adsorption capacity for heavy metal ions. Experimental factors such as pH, temperature, adsorption capacity, and ionic strength affecting metal ion removal have also been explored.

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.

PEI-Schiff base-modified mesoporous silica materials SBA-12, 15 and 16 for toxic metal ions capture (Co(II), Ni(II) and Cu(II)): Effect of morphology, post-synthetic modification and kinetic study

A series of SBA materials (SBA-12, SBA-15, and SBA-16) with polyethyleneimine (PEI) and its Schiff base variants with salicylaldehyde-modified samples (PS) have been successfully prepared and characterized. The synthesized materials were investigated by infrared spectroscopy (FT-IR), and quantification of the organic part coated on the surface was studied using thermogravimetric analysis (TGA). Nitrogen adsorption/desorption analysis at − 196 °C (N2), bright field scanning transmission electron microscopy (BF-STEM) and small angle X-ray scattering (SAXS) measurements were used to study textural properties, structure and morphology. Confirmation of heavy metal ions capture in pores of prepared materials was proved by X-ray fluorescence analysis (XRF), and nitrate anions were confirmed by FT-IR spectroscopy. Kinetic studies were performed by conductometric analysis (CA) and showed that the mathematical models could be applied to adsorption processes with a non-linear decreasing trend. This trend appeared in PS-modified SBA systems and some non-modified samples. The best overall adsorption properties were observed for material SBA-12 and its modified types. In this case, material SBA-12-PS can trap 54.38 mg g−1 of Cu(NO3)2 or 18.42 mg of Cu(II) ions, 112.84 mg g−1 of Ni(NO3)2 corresponding to 36.24 mg of Ni(II) cations, and 39.56 mg g−1 of Co(NO3)2 representing 12.74 mg of Co(II) ions. Non-modified materials show morphological effects where 2D ordered pores with hexagonal symmetry and the biggest mesopores (5.5 nm) have the best overall results in adsorption capacity of metal ions (Cu(II): 11.95 mg g−1) calculated from pseudo-second order. SBA-12 with a cubic framework and 3D ordered pores (3.8 nm) has a lower adsorption capacity than SBA-15 (Cu(II): 7.85 mg g−1), and SBA-16 with the smallest spherical pores (under 2 nm) showed the lowest overall adsorption capacity (Cu(II): 4.65 mg g−1). Kinetic rates of non-modified samples have opposite trend SBA-12 (Cu(II): 0.009 mg g−1 min−1) > SBA-15 (Cu(II): 0.002 mg g−1 min−1) > SBA-16 (Cu(II): 0.001 mg g−1 min−1). In the case of SBA-16, small pore entrances have a negative effect on the kinetic rate. For modified samples, SBA-12 with the largest surface area (896 m2 g−1) provides more space for binding of polyethyleneimine molecules (and also salicylaldehyde), which affects the best results in ion capture (Cu(II): 16.64 mg g−1). Bigger mesopores give more adsorption capacity, but capillarity makes the kinetic rate slow. SBA-16, with tiny entrance mesopores, has the lowest kinetic rate and adsorption capacity. This phenomenon was also observed in cobalt(II) adsorption, and similar results were obtained in nickel(II) adsorption. Kinetic studies point to two types of mechanisms given by the pseudo-second-order model in the case of non-modified materials, and Elovich kinetic model describes chemisorption at modified samples. These mechanisms are influenced by the significant effect of intraparticle diffusion, described by the Weber-Morris model.

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.

Dendritic Structure-Inspired Coating Strategy for Stable and Efficient Solar Evaporation of Salinity Brine

Solar thermal evaporation has been widely used to tackle the problem of freshwater shortage. The strategy to improve the evaporative performance of solar thermal evaporation by simple and effective methods is still a challenge. Herein, a dendritic structure-inspired coating strategy based on the dendritic structure of polyvinyl alcohol (PVA) colloids firmly grabbing titanium trioxide (Ti2O3) on the outer surface as a light-absorbing core–shell filler was prepared using the non-solvo-induced precipitation method. Such a core–shell structure was then coated on the PVA sponge to prepare the solar photothermal composite Ti2O3/PVA@PVA, which gave full play to the photothermal advantage of the filler itself and can be long-term stable. Meanwhile, a three-dimensional Ti2O3/PVA@PVA evaporator with an embossment-sawtooth structure was prepared, which enhances light absorption to 98% in the whole solar spectrum through folds. Under 1.0 solar irradiation, the evaporation rate reaches as high as 2.66 kg m–2 h–1 and the evaporator illustrates good stability in simulated seawater for 7 consecutive days. Such a design showed good salt resistance and self-cleaning ability and could be reliably used for seawater desalination. In addition, the evaporator illustrates good adsorption capacity for dye molecules and heavy metal ions. This work provides new insights into the development of simple, efficient, environmentally friendly, sustainable, and salt-resistant solar evaporators.

Evaluation of Fe3O4-MnO2@RGO magnetic nanocomposite as an effective persulfate activator and metal adsorbent in aqueous solution.

A reduced graphene oxide (RGO) supported Fe3O4-MnO2 nanocomposite (Fe3O4-MnO2@RGO) was successfully prepared for catalytic degradation of oxytetracycline (20mg/L) by potassium persulfate (PS) and adsorption removal of mixture of Pb2+, Cu2+, and Cd2+ ions (each 0.2mM) in the synchronous scenario. The removal efficiencies of oxytetracycline, Pb2+, Cu2+, and Cd2+ ions were observed as high as 100%, 99.9%, 99.8%, and 99.8%, respectively, under the conditions of [PS]0 = 4mM, pH0 = 7.0, Fe3O4-MnO2@RGO dosage = 0.8g/L, reaction time = 90min. The ternary composite exhibited higher oxytetracycline degradation/mineralization efficiency, greater metal adsorption capacity (Cd2+ 104.1mg/g, Pb2+ 206.8mg/g, Cu2+ 70.2mg/g), and better PS utilization (62.6%) than its unary and binary counterparts including RGO, Fe3O4, Fe3O4@RGO, and Fe3O4-MnO2. More importantly, the ternary composite had good magnetic recoverability and excellent reusability. Notably, Fe, Mn, and RGO could play a synergistic role in the improvement of pollutant removal. Quenching results indicate that surface bounded SO4•- was the major contributor to oxytetracycline decomposition, and the -OH groups on the composite surface shouldered a significant role in PS activation. The results indicate that the magnetic Fe3O4-MnO2@RGO nanocomposite has a good potential for removing organic-metal co-contaminants in waterbody.

Designed synthesis of multifunctional lignin-based adsorbent for efficient heavy metal ions removal and electromagnetic wave absorption

Multifunctional lignin-based adsorbents, which have shown great application prospect, have attracted widespread attention. Herein, a series of multifunctional lignin-based magnetic recyclable adsorbents were prepared from carboxymethylated lignin (CL), which was rich in carboxyl group (-COOH). After optimizing the mass ratio of CL to Fe3O4, the prepared CL/Fe3O4 (3:1) adsorbent showed efficient adsorption capacities for heavy metal ions. The kinetic and isotherm nonlinear fitting studies revealed that the adsorption process followed the second-order kinetic and Langmuir models, and the maximum adsorption capacities (Qmax) of CL/Fe3O4 (3:1) magnetic recyclable adsorbent for Pb2+, Cu2+ and Ni2+ ions reached 189.85, 124.43 and 106.97 mg/g, respectively. Meanwhile, after 6 cycles, the adsorption capacities of CL/Fe3O4 (3:1) for Pb2+, Cu2+ and Ni2+ ions could keep at 87.4 %, 83.4 % and 82.3 %, respectively. In addition, CL/Fe3O4 (3:1) also exhibited excellent electromagnetic wave absorption (EMWA) performance with a reflection loss (RL) of −28.65 dB at 6.96 GHz under the thickness of 4.5 mm, and its effective absorption bandwidth (EAB) achieved 2.24 GHz (6.08–8.32 GHz). In short, the prepared multifunctional CL/Fe3O4 (3:1) magnetic recyclable adsorbent with outstanding adsorption capacity for heavy metal ions and superior EMWA capability opens a new avenue for the diversified utilization of lignin and lignin-based adsorbent.