Efficiency and mechanism of enhanced norfloxacin removal using amorphous TiO2-modified biochar.

Inadequate treatment of antibiotic-contaminated wastewater, including compounds such as norfloxacin (NOR), poses a substantial treat to both ecological safety and human well-being. An innovative approach was devised to address NOR pollution using amorphous TiO2 modified biochar (A-TiO2/BC) prepared via sol-gel impregnation. The resultant had a commendably specific surface area of 131.8 m2/g-1, which was 1.91 times more than the original surface area of unmodified BC. A-TiO2/BC also exhibited abundant hydroxyl and oxygen-containing functional groups, thereby provided adequately active sites for NOR adsorption. R2 values obtained from NOR isotherm adsorption models descended in order of Freundlich < Temkin < Sips < Langmuir, which indicated that the NOR removal by A-TiO2/BC mainly complied with monolayer adsorption accompanied by heterogeneous surface adsorption. Under weakly acidic conditions, NOR adsorption benefits from the synergistic physicochemical interactions of A-TiO2 and BC. Notably, A-TiO2/BC demonstrated an impressive NOR adsorption capacity of up to 78.14 mg g-1, with a dosage of 20 mg L-1 at 25 °C under pH 6. Such A-TiO2 modified biochar thus presents a promising alternative for NOR removal.

Detoxification of corn stover prehydrolysate by different biochars and its effect on lactic acid fermentation.

During the utilization of lignocellulosic biomass such as corn stover, many by-products are produced in the pretreatment process that can severely inhibit the activity of microbes in the fermentation step. To achieve efficient biomass conversion, detoxification is usually required before microbial fermentation. In this study, the prehydrolysate from dilute acid pretreatment of corn stover was used as a lactic acid fermentation substrate. Biochars made from corn stover (CSB), cow manure (CMB), and a mixture of corn stover and cow manure (MB) were applied for the detoxification of the prehydrolysate. All three types of biochar had a porous structure with a specific surface area ranging from 4.08 m2 g-1 (CMB) to 7.03 m2 g-1 (MB). After detoxification, both the numbers of inhibitors and their concentrations in the prehydrolysate decreased, indicating that the biochars prepared in this study were effective in inhibitor removal. The concentration of lactic acid obtained from the prehydrolysate without detoxification was only 12.43 g L-1 after fermentation for 96 h with a productivity of 0.13 g (L h)-1. Although the specific area of CMB was the lowest among the three biochars, the CMB-treated prehydrolysate resulted in the highest lactic acid concentration of 39.25 g L-1 at 96 h with a productivity of 0.41 g (L h)-1. The lactic acid bacteria in the CMB-treated prehydrolysate grew faster than the other two biochars, reaching an OD value of 8.12 at 48 h. The results showed promise for the use of agricultural wastes to make biochar to increase the yield of lactic acid fermentation through the detoxification process.

Enhanced Enzymatic Sugar Recovery of Dilute-Acid-Pretreated Corn Stover by Sodium Carbonate Deacetylation.

The prehydrolysate from dilute acid pretreatment of lignocellulosic feedstocks often contains inhibitory compounds that can seriously inhibit the subsequent enzymatic and fermentation processes. Acetic acid is one of the most representative toxic compounds. In this research, alkaline deacetylation of corn stover was carried out using sodium carbonate under mild conditions to selectively remove the acetyl groups of the biomass and reduce the toxicity of the prehydrolysate. The deacetylation process was optimized by adjusting factors such as temperature, treatment time, and sodium carbonate concentration. Sodium carbonate solutions (2~6 wt%) at 30~50 °C were used for the deacetylation step, followed by dilute acid pretreatment with 1.5% H2SO4 at 121 °C. Results showed that the acetyl content of the treated corn stover could be reduced up to 87%, while the hemicellulose loss remained low. The optimal deacetylation condition was found to be 40 °C, 6 h, and 4 wt% Na2CO3, resulting in a removal of 80.55% of the acetyl group in corn stover and a hemicellulose loss of 4.09%. The acetic acid concentration in the acid prehydrolysate decreased from 1.38 to 0.34 g/L. The enzymatic hydrolysis of solid corn stover and the whole slurry after pretreatment increased by 17% and 16%, respectively.

Hypoxic Preconditioning Modulates BDNF and Its Signaling through DNA Methylation to Promote Learning and Memory in Mice.

Hypoxic preconditioning (HPC) as an endogenous mechanism can resist hypoxia/ischemia injury and exhibit protective effects on neurological function including learning and memory. Although underlying molecular mechanisms remain unclear, HPC probably regulates the expression of protective molecules by modulating DNA methylation. Brain-derived neurotrophic factor (BDNF) activates its signaling upon binding to the tropomyosin-related kinase B (TrkB) receptor, which is involved in neuronal growth, differentiation, and synaptic plasticity. Therefore, this study focused on the mechanism by which HPC regulates BDNF and BDNF/TrkB signaling through DNA methylation to influence learning and memory. Initially, the HPC model was established by hypoxia stimulations on ICR mice. We found that HPC downregulated the expression of DNA methyltransferase (DNMT) 3A and DNMT3B. Then, the upregulation of BDNF expression in HPC mice was generated from a decrease in DNA methylation of the BDNF gene promoter detected by pyrophosphate sequencing. Subsequently, upregulation of BDNF activated BDNF/TrkB signaling and ultimately improved learning and spatial memory in HPC mice. Moreover, after mice were intracerebroventricularly injected with the DNMT inhibitor, the restraint of DNA methylation accompanied by an increase of BDNF and BDNF/TrkB signaling was also discovered. Finally, we observed that the inhibitor of BDNF/TrkB signaling prevented HPC from ameliorating learning and memory in mice. However, the DNMT inhibitor promoted spatial cognition in mice. Thus, we suggest that HPC may upregulate BDNF by inhibiting DNMTs and decreasing DNA methylation of the BDNF gene and then activate BDNF/TrkB signaling to improve learning and memory in mice. This may provide theoretical guidance for the clinical treatment of cognitive dysfunction caused by ischemia/hypoxia disease.

Adsorption Mechanism of Amidoxime Collector on the Flotation of Lepidolite: Experiment and DFT Calculation.

Lepidolite is an important mineral resource of lithium. With the increase in awareness of low-carbon and green travel, the demand for lithium has increased dramatically. Therefore, how to increase the output of lithium has to turn into high precedence. In this paper, amidoxime (DPA) was synthesized and used for the efficient collection of lepidolite. Dodecylamine (DA), a commonly used collector of lepidolite ore, was used for comparison. The collecting performances of DA and DPA for lepidolite were studied by the micro-flotation experiment, and the adsorption mechanism of DPA on lepidolite was verified by contact angle, zeta potential tests, FTIR spectra, and density functional theory (DFT) calculations. The results of flotation experiments showed that at the same collector dosage (3 × 10-4 mol/L), the recovery of lepidolite could reach 90%, while the recovery of lepidolite with DA was only 52.5%, and to achieve the maximum recovery of DA (77.5%), only half of the DPA was added. The contact angle test results showed that DPA could effectively improve the hydrophobicity of lepidolite than DA. FTIR spectra and zeta potential tests suggested that DPA molecules were adsorbed on the lepidolite surface by electrostatic attraction. DFT calculations revealed that DPA reacted with the nucleophilic reagent (lepidolite) by the reactive site of the -CH2NH(CH2)2C(NOH)N+H3 group and more easily absorbed on the surface of lepidolite than DA. Therefore, our new finding will provide an important prospect for the sustainable development and utilization of lithium resources.

The atmospheric microplastics deposition contributes to microplastic pollution in urban waters.

Identifying and understanding the potential sources delivering microplastics into the urban water environment is imperative for microplastic pollution control. However, how atmospheric deposition contributes to microplastic pollution in the urban water environment is unclear. Therefore, this study investigated the contribution of atmospheric deposition to microplastic pollution in urban waters based on the analysis of the atmospheric deposition characteristics in the urban area. The results showed that microplastic deposition fluxes during wet weather and dry weather varied from 1.1 × 103±0.06×103 to 3.5 × 103±0.3 × 103 particles/m2/day and 0.91×103±0.09×103 to 1.6 × 103±0.1 × 103 particles/m2/day, respectively. The microplastics deposition flux showed moderate to strong correlations to atmospheric particulate matter concentrations, especially the PM2.5 concentration (R2 = 0.76-0.93), suggesting the regularly monitored PM2.5 concentration might be served as an indicator for microplastics deposition flux estimation. The deposited microplastics were mainly transparent fragments with an average size of 51-67 µm. Polyethylene and polypropylene were the most abundant plastic polymer, followed by polyethylene terephthalate and polyamide. The comparison of microplastics collected during different weather conditions suggested that rain events could increase microplastics deposition fluxes when air quality conditions are similar. Particularly, rains promoted the deposition of fibrous microplastics as well as smaller microplastics. The estimated daily microplastics deposition in the whole city region suggested more microplastics were deposited in summer and winter. The total quantity of microplastics deposited in the urban environment could reach 1.7-12 times of those discharged from treated wastewater. Among them, 10% would directly deposit to urban waters in the studied city region, while the others may also enter the urban waters through runoff. The results of this study highlighted that the atmospheric microplastics deposition is an important source for microplastics, especially smaller ones, to enter the urban waters, which could not be ignored during microplastics pollution control.

Iron ore production using a new Gemini surfactant at 273 K.

Herein we present the use of a Gemini surfactant and reverse froth flotation to efficiently separate magnetite from quartz and produce iron ore at 273 K. This surfactant achieved an obviously superior flotation performance (TFe recovery increased by 48.18%), and the dosage of the Gemini surfactant was three times less than that of a conventional monomeric surfactant. Our findings are expected to serve as a general guide to design a new and excellent collector for high-efficiency mineral flotation and to lead to an efficient and clean development of mineral resources.

Adsorption of Trisiloxane Surfactant for Selective Flotation of Scheelite from Calcite at Room Temperature.

The separation and enrichment of scheelite from calcite are hindered by the similar active Ca2+ sites of scheelite and the calcite with calciferous gangue. Herein, a novel trisiloxane surfactant, N-(2-aminoethyl)-3-aminopropyltrisiloxane (AATS), was first explored and synthesized and recommended as the collector for the flotation separation of scheelite from calcite. The micro-flotation and mixed binary mineral flotation tests showed that AATS had excellent collection performance for scheelite and high selectivity for calcite within a wide pH range. At the same time, contact angle and zeta-potential measurements, Fourier transform infrared (FTIR) analysis, and density functional theory (DFT) calculations revealed the relevant adsorption mechanism. The contact angle measurement showed that AATS can increase the contact angle of the scheelite surface from 41.7 to 95.8°, greatly enhancing the hydrophobicity of the mineral surface. The results of FTIR analysis and zeta-potential measurement explained that AATS was electrostatically adsorbed on the mineral surface, and DFT calculation further verified that the -N+H3-positive group in AATS was adsorbed on the negatively charged scheelite surface. Therefore, AATS can realize the expectation of high efficiency and selectivity of minerals and enhance the adhesion between the surface of scheelite minerals and bubbles, providing a fresh approach to industrial production.

Recovery of wolframite from tungsten mine tailings by the combination of shaking table and flotation with a novel "crab" structure sebacoyl hydroxamic acid.

Tailings ponds for gangue mineral storage are widely recognized as a dangerous source of toxic minerals and heavy metal-bearing solution. Therefore, recovering valuable minerals and critical elements from tailings is an important means to protect the environment in an economic way. Wolframite tailings usually contain a considerable amount of tungsten resources, but the presence of high content of kaolinite sludge makes it very difficult to recycle wolframite. Herein, a novel sebacoyl hydroxamic acid (SHA) was synthesized and introduced as a novel wolframite collector to effectively utilize wolframite tailings, and its collection performance was compared with that of benzohydroxamic acid (BHA). Micro-flotation tests showed that SHA could still obtain 80% wolframite recovery in the presence of kaolinite slimes. Bench-scale flotation tests indicated that SHA can effectively recover wolframite concentrate with 55.64% WO3 grade and 75.28% WO3 recovery from wolframite tailings by the combined shaking table-flotation process. Polarized light microscope observations showed that SHA could promote the formation of hydrophobic agglomerates of wolframite particles. These results show that SHA can be used as an efficient collector for disposing of wolframite tailings, and provide an important reference for the development of efficient and comprehensive utilization of tailings.

Copper single-atom catalyst as a high-performance electrocatalyst for nitrate-ammonium conversion.

Electrocatalytic nitrate reduction reaction (NO3RR), as a promising alternative to the Haber-Bosh process, provides new opportunities for ammonia (NH3) production from the environmental and energy viewpoint. However, the NH3 yield rate and selectivity for NO3RR are still limited due to the lack of efficient electrocatalysts. Herein, we demonstrate an active and selective copper single-atom catalyst (Cu-N-C) for nitrate reduction to NH3. The complete conversion of nitrate (50 mg L-1 NO-3-N) was achieved at -1.5 V vs. SCE with a high NH3 yield rate (9.23 mg h-1 mg-1cat.) and selectivity (94%). Remarkably, Cu-N-C dramatically inhibited the formation of toxic nitrite and double-nitrogen products due to the enhanced nitrite adsorption and restrained N-N coupling that led to nitrate deep reduction to NH3. The remaining nitrate (0.06 mg L-1) and nitrite (1 mg L-1) fully meet the drinking-water standards. Density functional theory simulations reveal that the single-site nature of Cu-N-C facilitated the reduction of HNO*3 to NO*2 and NH*2 to NH3, thus leading to the selective nitrate reduction to NH3.

Medium-chain fatty acids production from carbohydrates-rich wastewater through two-stage yeast biofilm processes without external electron donor addition: Biofilm development and pH impact.

The production of medium-chain fatty acids (MCFAs) is considered promising for carbon resource recovery from waste streams. However, a large quantity of external electron donors are often required, causing great cost and environmental impact. Therefore, in this study, a two-stage technology was developed to produce MCFAs from carbohydrate-rich wastewater without external electron donor addition, with the biofilm development and pH impact being explored. Stage I aimed at converting organics into ethanol and a yeast biofilm reactor is innovatively applied. The results showed that the yeast biofilm could quickly form on carriers with steady-state thickness reaching 50-200 µm. However, the attachment of yeast biofilm was weak at the initial stage so that the violent turbulence should be avoided during operation. The polyurethane foam was the most suitable for yeast biofilm development among the tested carriers, as evidenced by the highest ethanol production, accounting for 74.2% of soluble organics. The Nakaseomyces was the main fungal genus in the steady-state biofilm, while lactic acid bacteria were also developed, resulting in lactate and acetate production. In Stage II, the yeast biofilm reactor effluent was applied for MCFA production at different pH (5-8). However, the MCFA production selectivity was significantly affected by pH, with 65.2% at pH of 5 but decreasing substantially to 3.0% at pH of 8. Both the microbial and electron transfer efficiency analysis suggested that mildly acidic pH can promote the electron transfer from ethanol toward the chain elongation process instead of its excessive oxidation. Thus, if conditions of online extraction or microbial tolerance permit, a lower pH should be recommended for Stage II in the developed technology as well as other ethanol-based MCFA production process. This is a conceptual study that eliminated external electron donor addition in MCFAs production and provide a sustainable and reliable way in carbon resources recovery.

A comparative review of microplastics in lake systems from different countries and regions.

Microplastics, as defined here as plastics with a diameter of <5 mm, can impose severely detrimental impacts on the environment and can now be commonly found in different water bodies. To date, the status of microplastics in limnic systems, which have different hydrologic systems compared to other water bodies such as oceans or rivers, has rarely been reviewed. In the present study, the microplastic pollutants in different countries and regions were comparatively investigated in terms of their abundances, morphologies, and polymer types in the water and sediments of lakes. The concentration and characteristics of microplastics were found to be largely different across countries and regions, which was related to the local development level and economic structure. The migration paths of microplastics in the inner and external limnic ecosystems further revealed the causes for the regional divergence in microplastics. Policy developments in different countries and regions were also discussed to highlight the urgency of better controlling microplastic pollution in lake systems. The characteristics of microplastics vary across countries and regions, depending on the local development level and economic structure.

Understanding the mobility and retention of uranium and its daughter products.

Knowledge of the behavior of technologically enhanced naturally occurring radioactive materials derived through the decay of U and its daughter products, and their subsequent fractionation, mobilization and retention, is essential to develop effective mitigation strategies and long-term radiological risk prediction. In the present study, multiple state-of-the-art, spatially resolved micro-analytical characterization techniques were combined to systematically track the liberation and migration of radionuclides (RN) from U-bearing phases in an Olympic Dam Cu flotation concentrate following sulfuric-acid-leach processing. The results highlighted the progressive dissolution of U-bearing minerals (mainly uraninite) leading to the release, disequilibrium and ultimately upgrade of daughter RN from the parent U. This occurred in conjunction with primary Cu-Fe-sulfide minerals undergoing coupled-dissolution reprecipitation to the porous secondary Cu-mineral, covellite. The budget of RN remaining in the leached concentrate was split between RN still hosted in the original U-bearing minerals, and RN that were mobilized and subsequently sorbed/precipitated onto porous covellite and auxiliary gangue mineral phases (e.g. barite). Further grinding of the flotation concentrate prior to sulfuric-acid-leach led to dissolution of U-bearing minerals previously encapsulated within Cu-Fe-sulfide minerals, resulting in increased release and disequilibrium of daughter RN, and causing further RN upgrade. The various processes that affect RN (mobility, sorption, precipitation) and sulfide minerals (coupled-dissolution reprecipitation and associated porosity generation) occur continuously within the hydrometallurgical circuit, and their interplay controls the rapid and highly localized enrichment of RN. The innovative combination of tools developed here reveal the heterogeneous distribution and fractionation of the RN in the ores following hydrometallurgical treatment at nm to cm-scales in exquisite detail. This approach provides an effective blueprint for understanding of the mobility and retention of U and its daughter products in complex anthropogenic and natural processes in the mining and energy industries.

Mechanistic study on calcium ion diffusion into fayalite: A step toward sustainable management of copper slag.

Copper slag, which contains Fe-rich fayalite (Fe2SiO4), is a valuable solid waste that warrants further research in order to recover iron. Calcium oxide (CaO) can significantly enhance iron recovery from copper slag; however, the associated mechanism has not yet been explored. In this study, we investigated the interaction between CaO and Fe2SiO4 to obtain detailed understanding of the role of CaO in enhancing iron recovery. The presence of CaO was found to accelerate the decomposition of Fe2SiO4 via an ion-exchange-like process. Specifically, CaO dissociated into Ca(II) and a Ca-deficient Ca1-yO species at high temperatures. The Fe(II) ion at the M2 site of Fe2SiO4 was substituted by the released Ca(II) ion, resulting in the formation of [(Fe(2-x)Cax)SiO4]∙xFe(II). Subsequently, the substituted Fe(II) occupied the Ca vacancy in Ca1-yO to form (Ca(1-y)Fe(II)y)O. The disproportionation of Fe(II) and the combination reaction between CaO and the SiO2 separated from Fe2SiO4 led to the generation of the final products, viz. Fe2O3, Fe3O4, and CaSiO3. This study explains the specific role of CaO in decomposing Fe2SiO4. It would not only provide theoretical guidance for iron recovery from copper slag but also present a new perspective on the recycling of valuable resources from many other smelting slags (e.g., iron slag, lead slag, and nickel slag).

"Umbrella" Structure Trisiloxane Surfactant: Synthesis and Application for Reverse Flotation of Phosphorite Ore in Phosphate Fertilizer Production.

Phosphorite is generally used in the manufacture of phosphate fertilizer and plays a vital role in the development of agricultural and food production. Nonetheless, how to obtain phosphorite concentrates efficiently and sustainably has become an urgent problem. In this study, a newly designed trisiloxane surfactant, N-(2-Aminoethyl)-3-aminopropyltrisiloxane (AATS), has been prepared and utilized as an emerging collector for reverse flotation of phosphorite ore. Its collecting ability was compared with the conventional surfactant 1-dodecamine (DDA). In the collector concentration tests, AATS with lower concentrations showed stronger collecting ability for quartz. In the pH tests, AATS always performed better than DDA in the acidic or alkaline condition. In bench-scale flotation experiments, the P2O5 recovery of phosphorite concentrates with 150 g/t AATS was 10.77% higher than that with 300 g/t DDA, which proved that AATS can be applied to the sustainable production of phosphorite concentrates. For a 4000 t/d phosphorite ore processing plant, the profit could be increased 7,014,702.07 USD every year by using AATS as the collector. Therefore, this work provides a promising approach to enhance the production efficiency of phosphate fertilizer and to promote the sustainable development of agriculture.

Validity of ICD-10-CM Codes Used to Identify Patients with Chronic Hepatitis B and C Virus Infection in Administrative Claims Data from the Taiwan National Health Insurance Outpatient Claims Dataset.

PURPOSE: To validate the use of International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) codes to identify patients with chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infection in the Taiwan National Health Insurance (NHI) Outpatient Claims Dataset. METHODS: We conducted a retrospective study using results of HBV surface antigen (HBsAg), HBV e antigen (HBeAg), and anti-HCV antibody tests in the NHI Lab & Exam Dataset from January 1 to March 31, 2018, as the reference standard to confirm HBV and HCV infection cases. We calculated sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) to assess the performance of HBV infection-specific ICD-10-CM codes (B180, B181, and B191) and HCV infection-specific ICD-10-CM codes (B182 and B192) recorded in the NHI Outpatient Claims Dataset to identify patients with HBV or HCV infection. RESULTS: In total, 196,635 and 120,628 patients had analyzable results for HBsAg/HBeAg tests and anti-HCV tests, respectively. Moreover, 44,574 and 14,443 were confirmed to have HBV and HCV infection, respectively. The sensitivity, specificity, PPV, and NPV were, respectively, 46%, 83%, 45%, and 84% for HBV infection-specific ICD-10-CM codes and 47%, 99%, 81%, and 93% for HCV infection-specific ICD-10-CM codes. The sensitivity demonstrated great variation by region, clinical setting, and physician specialty. CONCLUSION: The HBV and HCV infection-specific ICD-10-CM codes recorded by physicians in Taiwan NHI outpatient claims data in 2018 had moderate sensitivity and high specificity for both HBV and HCV infection. The PPV was high for HCV ICD-10-CM codes, yet moderate for HBV ICD-10-CM codes.

Poly(diallyldimethylammonium-MoS4) based amorphous molybdenum sulphide composite for selectively mercury uptake from wastewater across a large pH region.

Amorphous molybdenum sulphide materials are attracting more attention in heterogeneous catalysis, gas adsorption and water remediation fields. Herein, a new type of amorphous molybdenum sulphide composite (poly(diallyldimethylammonium-MoS4), shorten as PDADMA-MoS4) was synthesized via a facile precipitation reaction. Metal adsorption tests of prepared PDADMA-MoS4 composite shows that Hg2+ and Pb2+ concentrations in solution can decrease from 10 ppm to <0.5 ppb level much lower than the drinking water requirement (<2 ppb) in 10 min. The metal adsorption isotherms suggest that maximum metal-uptake capacities are 1460.0 mg/g for Hg (pH = 5) and 433.7 mg/g for Hg (pH = 1), indicating that this sorbent works over a wide pH range (1.0-7.0) to effectively remove Hg from aqueous solution. More importantly, at very low pH = 1, this sorbent material exhibits extraordinarily high selectivity of Hg over Pb and Cu (separation factors ßHg/Cu=4.5×104 and ßHg/Pb=3.6×104). The excellent Hg capacity and selectivity at low pH region (pH < 2) has shed light on the new generation of adsorbent materials for acidic wastewater treatment.

Specific ion binding interactions in potash flotation.

As the main resource of potash fertilizer, high grade of sylvite (KCl) is mainly separated from halite (NaCl) in soluble potash ores using flotation. An effective flotation collector determines the separation efficiency of sylvite. However, the collector adsorption mechanism is still the subject of much debate due to high ions concentration in the flotation pulp. This paper studies the hydration status of KCl, the flotation behavior of KCl and NaCl with lauric acid and the interfacial water structure of the soluble salts to provide further insights into the fundamental mechanisms at play. The contact angle measurements and laboratory micro-flotation experiments have shown that both the hydration status of KCl and the flotation soluble salts with lauric acid were dependent on the solution composition. Specifically, it was determined that the addition of Na-ions had an adverse effect on the hydrophobicity of KCl crystals. Both KCl and NaCl can be floated with lauric acid. However, flotation of NaCl is greatly enhanced with the addition of K-ions whereas the flotation of KCl is suppressed with the addition of Na-ions. Sum frequency generation (SFG) measurements have found, most strikingly, more disordered water molecules dominating the "structure maker" salt surfaces in a saturated NaCl solution. "Collins Concept" is employed to explain the specific ion binding behaviors in the flotation pulp.

Remarkable reusability of magnetic Fe3O4-encapsulated C3N3S3 polymer/reduced graphene oxide composite: A highly effective adsorbent for Pb and Hg ions.

Magnetic Fe3O4-encapsulated C3N3S3 polymer/reduced graphene oxide composite (rGO-poly(C3N3S3)/Fe3O4) was synthesized to remove Pb(II) and Hg(II) from aqueous solutions. This material was characterized by X-ray Photoelectron Spectroscopy, transmission electron microscopy, Fourier-transform infrared spectroscopy, X-ray powder diffraction, N2 adsorption, etc. The results suggest that final composite exhibits two-dimensional (2D) nanosheet structure, in which Fe3O4 nanoparticles or clusters are encapsulated between the layers of rGO-poly(C3N3S3) matrix, preventing composite aggregation and nanoparticle detachment. The results of adsorption tests suggested high metal removal and short residence time to reach equilibrium. The adsorption kinetics data were well fitted by pseudo-second-order equation. The effect of metal concentration on adsorption was illustrated by Langmuir isotherm equation. Maximum metal-uptake capacities for Pb(II) and Hg(II) ions were 270.3 and 400.0 mg/g, respectively. High-resolution XPS spectra clearly illustrate the adsorption mechanism, in that Hg(II) preferentially binds to sulphur functional groups and Pb(II) tends to be adsorbed by nitrogen groups in poly(C3N3S3) matrix. Recycling performance of this composite was investigated in 15 consecutive adsorption-desorption cycles, after which the adsorption capacities for Pb(II), and Hg(II) ions remain stable thanks to Fe3O4 encapsulation into the rGO-poly(C3N3S3) matrix.