Dewatering behavior and regulation mechanism of montmorillonite nanosheet in aqueous solution.

Two-dimensional montmorillonite nanosheet (MMTNS) is desirable building block for fabricating multifunctional materials as due to its extraordinary properties. In practical applications, however, the concentration of MMTNS prepared by exfoliation is normally too low to be used for material assembling. The general thermal-concentration method is effective, however, it can be time-consuming and require a lot of energy. In this case, the remarkable dispersion stability of MMTNS is worth noting. Herein, the extraordinary dispersion stability of MMTNS derived from electrostatic and hydration repulsion was firstly revealed by molecular dynamics (MD) simulation, which caused the poor dewatering of MMTNS. Further, based on the surface and structural chemistry of MMTNS, a series of strategies, involving charge and cross-linked structure regulation on the edge surface, as well as electrical double-layer modulation and calcification modification based on the electrolytes, were proposed to inhibit the dispersion and enhance the aggregation of MMTNS. Intriguingly, a novel chemical, Tetraethylenepentamine (TEPA) was applied in the dewatering of MMTNS. The TEPA not only act as a cross-linker to bond with MMTNS into an easy-to-dewatering 3D network structure, but also act as a switch for effortless viscosity tuning. Meanwhile, the dual function of electrolytes for electrical double layer compression and calcification modification of MMTNS was investigated by DLVO theory and structural analyses. This work offers explicit directions for improving the dewatering performance of MMTNS to meet the requirements of practical implementation.

Quantitative Analysis of Mixed Minerals with Finite Phase Using Thermal Infrared Hyperspectral Technology.

It is crucial but challenging to detect intermediate or end products promptly. Traditional chemical detection methods are time-consuming and cannot detect mineral phase content. Thermal infrared hyperspectral (TIH) technology is an effective means of real-time imaging and can precisely capture the emissivity characteristics of objects. This study introduces TIH to estimate the content of potassium salts, with a model based on Competitive Adaptive Reweighted Sampling (CARS) and Partial Least Squares Regression (PLSR). The model takes the emissivity spectrum of potassium salt into account and accurately predicts the content of Mixing Potassium (MP), a mineral mixture produced in Lop Nur, Xinjiang. The main mineral content in MP was measured by Mineral Liberation Analyzer (MLA), mainly including picromerite, potassium chloride, magnesium sulfate, and less sodium chloride. 129 configured MP samples were divided into calibration (97 samples) and prediction (32 samples) sets. The CARS-PLSR method achieved good prediction results for MP mineral content (picromerite: correlation coefficient of correction set (Rp2) = 0.943, predicted root mean square error (RMSEP) = 2.72%, relative predictive deviation (RPD) = 4.24; potassium chloride: Rp2 = 0.948, RMSEP = 2.86%, RPD = 4.42). Experimental results convey that TIH technology can effectively identify the emissivity characteristics of MP minerals, facilitating quantitative detection of MP mineral content.

Mobile Sources Are Still an Important Source of Secondary Organic Aerosol and Fine Particulate Matter in the Los Angeles Region.

Secondary organic aerosol (SOA) is a significant component of atmospheric fine particulate matter. Mobile sources have historically been a major source of SOA precursors in urban environments, but decades of regulations have reduced their emissions. Less regulated sources, such as volatile chemical products (VCPs), are of growing importance. We analyzed ambient and emissions data to assess the contribution of mobile sources to SOA formation in Los Angeles during the period of 2009-2019. During this period, air quality in the Los Angeles region has improved, but organic aerosol (OA) concentrations did not decrease as much as primary pollutants. This appears to be largely due to SOA, whose mass fraction in OA increased over this period. In 2010, about half of the freshly formed SOA measured in Pasadena, CA appears to be formed from hydrocarbon (non-oxygenated) precursors. Chemical mass balance analysis indicates that these hydrocarbon SOA precursors (including intermediate volatility organic compounds) can largely be explained by emissions from mobile sources in 2010. Our analysis indicates that continued reduction in emissions from mobile sources should lead to additional significant decreases in atmospheric SOA and PM2.5 mass in the Los Angeles region.

Enhanced removal of fluoride from water through precise regulation of active aluminum phase using CaCO3.

Coagulation with aluminum salts is an important method for fluoride removal from groundwater. However, the hydration of aluminum salts generating a large number of H+ usually leads to limited defluorination performance due to the optimum pH of active aluminum phase for fluoride removal around 5.5-6.5. In this work, enhanced fluoride removal from groundwater through precise regulation of active aluminum phase by CaCO3 was investigated. Precipitation products were characterized by XPS, FTIR, XRD, and SEM, respectively, and the mechanism of the high fluoride removal efficiency was discussed and compared with the traditional coagulation of Al2(SO4)3. In the Al2(SO4)3 + CaCO3 (ASCC) system, CaCO3 can stably regulate the pH at the optimum range for active aluminum phase existence and has the best fluoride removal effect. CaCO3 accurately regulated the activity of the aluminum phase by slowly releasing OH- and fine tuning pH, thereby achieving effective fluoride removal. Undissolved CaCO3 particles exist as the carrier of defluorination flocs to accelerate precipitation and improve stability. The work here provides a new method for fluoride removal and may shed light on the application of CaCO3 coagulants for other pollutants.

Precise Cation Recognition in Two-Dimensional Nanofluidic Channels of Clay Membranes Imparted from Intrinsic Selectivity of Clays.

Various kinds of clays occur naturally and are accompanied by particular cations in their interlayer domains. Here we report the reassembled membranes with nanofluidic channel arrays by using the natural clays montmorillonite, mica, and vermiculite, which were imparted with the natural selectivity for realizing precise recognition and directional regulation of the naturally occurring interlayer cations. A typical surface-governed ionic transport behavior was observed in the clay nanofluidic channels. Through asymmetric structural modification, cationic current rectification was realized in montmorillonite channels that performed as a nanofluidic diode. Interestingly, in the mica nanofluidic channel, the K+ that was naturally occurring in the interlayer domain of mica showed a reciprocating motion and resulted in a periodically fluctuating current. Electrodialysis demonstrated that such a fluctuating current reflects a directional selectivity for K+, achieving at least a 6000 times permeation rate difference with Li+ ions. The specific selectivity for Li+/Mg2+ on vermiculite reached up to 856 times with similar cations by the current technique. As-obtained clay membranes possess application prospects in energy conversion, brine resource development, etc. Such a strategy can achieve the designed selectivity through systematic screening of the building blocks, thus imparting them with the inherent characteristics of natural clays, which provides an alternative solution to the present manufacture of selective membranes.

Enhanced removal of refractory humic- and fulvic-like organics from biotreated landfill leachate by ozonation in packed bubble columns.

Biotreated landfill leachate contains much refractory organics such as humic and fulvic acids, which can be degraded by O3. However, the low O3 mass transfer and high energy cost limit its wide application in landfill leachate treatment. Previous studies proved that packed bubble columns could enhance the O3 mass transfer and increase the synthetic humic acids wastewater degradation, but the performance of packed bubble columns in real wastewater treatment has not been investigated. Therefore, this study aims to evaluate the feasibility of application of packed bubble column in the real biotreated landfill leachates treatment and provide insights into the transformation of organic matters in leachates during ozonation. Packed bubble columns with lava rocks or metal pall rings (LBC or MBC) were applied and compared with a non-packed bubble column (BC). At an applied O3 dose of 8.35 mg/(Lwater sample min), the initial COD (400 mg/L) was only removed for 26% in BC and 32% in MBC while this was 46% in LBC, indicating LBC has the best performance. GC-MS analysis shows that raw biotreated leachate contains potential endocrine disruptors such as di(2-ethylhexyl) phthalate (DEHP). 61% of DEHP was removed in LBC and the least intermediate oxidation products from humic- and fulvic-like organics was detected in LBC. The highest O3 utilization efficiency (89%) and hydroxyl radical (OH) exposure rate (3.0 × 10-10 M s) were observed in LBC with lowest energy consumption (EEO) for COD removal of 18 kWh/m3. The enhanced ozonation efficiency in LBC and MBC was attributed to the improved O3 mass transfer. Besides, LBC had additional adsorptive and catalytic activity that promoted the decomposition of O3 to generate OH. This study demonstrates that a packed bubble column increases removal and decreases energy use when treating landfill leachate, thus promoting the application of ozonation.

Synthetic Fe-rich nontronite as a novel activator of bisulfite for the efficient removal of tetracycline.

In this work, the iron-containing smectite nontronite (NNT) was artificially prepared by hydrothermal process and used as a heterogeneous catalyst to activate bisulfite (BS) for degradation of tetracycline (TC). Two NNT samples with different iron content (NNT1 and NNT2) were characterized by XRD, FTIR, XPS and SEM-EDS analysis. Under dark condition, the TC removal rates of NNT1/BS and NNT2/BS reached about 91.7% and 95.5% respectively at 60 min. Due to the heterogeneous catalysis of structural Fe(III), the NNT catalysts showed great catalytic activity and low iron leaching at the pH range 3.0-7.5. In addition, NNT particles were also stable and reusable in activating BS for TC removal. According to the EPR and radical quenching experiments, it could be proved that the precursor radical •SO3- was first generated in NNT/BS system, then •SO4- and •OH were the active species that played a role in TC degradation. The synthetic NNT clay is a promising Fe-based catalyst for treatment of TC wastewater thanks to its high activity, good stability and effective reusability.

Eco-friendly geopolymer prepared from solid wastes: A critical review.

Solid wastes are generated from human activities which could cause damage to the ecological environment and human beings. In recent years, there has been extensive research on solid wastes utilized as precursors, aggregates, fibers, etc. to prepare the geopolymers, which has invariably been a research hotspot. This review classifies the solid wastes utilized for geopolymers into three main categories: industrial waste, agricultural waste, and municipal waste. Accordingly, we systematically dissert solid wastes-based geopolymer from the perspectives of structure, properties, and application. The chemical composition, morphology, particle size, thermal conductivity, and other characteristics of solid wastes can trigger changes in the specific properties of geopolymers. On this account, solid wastes-based geopolymers have great potential in the domain of concrete, fireproof materials, impermeable materials, catalysts, adsorbents, and energy storage materials, etc. More importantly, geopolymers have obvious advantages in immobilizing heavy metals in solid wastes. Therefore, it can demonstrate geopolymer is a sustainable and environmentally friendly "green material". However, it still confronts the challenges of solid wastes utilized in geopolymer (technology, economy, administration). It requires the government, enterprises, and the public to work together for co-governance to accomplish industrialization and commercialization of solid wastes-based geopolymer.

Synthesis of carboxymethyl cellulose-chitosan-montmorillonite nanosheets composite hydrogel for dye effluent remediation.

MMTNS were introduced into carboxymethyl cellulose-chitosan system to synthesize porous hydrogel adsorbent with stable structure and high dye handling capacity. Al-OH on edge of MMTNS formed hydrogen-bond (-OH···+NH3-) with -NH2 on CS, CS then cooperated with CMC via amidation and chains interleaving, forming three-dimensional hydrogel. Morphology characterization revealed that hydrogel possessed microporous open-framework structure, facilitating free entrance of macromolecular MB dye to react with internal reaction sites in hydrogel. Factor tests indicated that high removal (97%) of MB was achieved via 0.2 g/L hydrogel within 360 min even after 5 adsorption-regeneration cycles. Adsorption process followed Pseudo-first-order, Pseudo-second-order kinetic model and Sips isotherm model, owing to both monolayer physical and chemical adsorption behavior of MB molecules onto homogeneous surface of hydrogel. Adsorption mechanism was attributed to ion-exchange, groups combination of carboxyl and hydroxyl, and Si active sites reaction. Such hydrogel realized promotion of polysaccharide polymers in materials design and wastewater treatment.

Role of Montmorillonite, Kaolinite, or Illite in Pyrite Flotation: Differences in Clay Behavior Based on Their Structures.

It is widely acknowledged that clay minerals have detrimental effects on the process of flotation, but the mechanisms involved are still not fully understood. In this work, the effects of montmorillonite, kaolinite, and illite on pyrite flotation were investigated from the perspective of various structures of clay minerals. Flotation tests suggested that the detrimental effect of clay minerals on the flotation of pyrite increased as follows: montmorillonite > kaolinite > illite. With the help of rheology measurements, it was found that montmorillonite significantly increased pulp viscosity, which in turn substantially reduced pyrite recovery and grade. Scanning electron microscopy (SEM) images suggested that montmorillonite formed the "house-of-cards" structure by edge-to-edge and edge-to-face contact, while kaolinite and illite platelets were associated mainly in the face-to-face mode. In addition, it was clearly observed by SEM-energy dispersive spectrometry that montmorillonite and kaolinite coat on the pyrite surfaces, which would lower the surface hydrophobicity of pyrite. Kaolinite covered much larger area of pyrite surface than montmorillonite owing to the positive charge occurring at the exposed aluminum-oxygen octahedral sheet of kaolinite. Although illite has a similar 2:1 structure to montmorillonite, it showed little or no effect on pyrite flotation, which was attributed to its poor swelling nature. These findings shed light on the root cause of the adverse effect of clay minerals on pyrite flotation and are expected to provide theoretical guidance for mitigating the negative effects on flotation caused by clays.

Simulation of organic aerosol formation during the CalNex study: updated mobile emissions and secondary organic aerosol parameterization for intermediate-volatility organic compounds.

We describe simulations using an updated version of the Community Multiscale Air Quality model version 5.3 (CMAQ v5.3) to investigate the contribution of intermediate-volatility organic compounds (IVOCs) to secondary organic aerosol (SOA) formation in southern California during the CalNex study. We first derive a model-ready parameterization for SOA formation from IVOC emissions from mobile sources. To account for SOA formation from both diesel and gasoline sources, the parameterization has six lumped precursor species that resolve both volatility and molecular structure (aromatic versus aliphatic). We also implement new mobile-source emission profiles that quantify all IVOCs based on direct measurements. The profiles have been released in SPECIATE 5.0. By incorporating both comprehensive mobile-source emission profiles for semivolatile organic compounds (SVOCs) and IVOCs and experimentally constrained SOA yields, this CMAQ configuration best represents the contribution of mobile sources to urban and regional ambient organic aerosol (OA). In the Los Angeles region, gasoline sources emit 4 times more non-methane organic gases (NMOGs) than diesel sources, but diesel emits roughly 3 times more IVOCs on an absolute basis. The revised model predicts all mobile sources (including on- and off-road gasoline, aircraft, and on- and off-road diesel) contribute ~ 1 µgm-3 to the daily peak SOA concentration in Pasadena. This represents a ~ 70% increase in predicted daily peak SOA formation compared to the base version of CMAQ. Therefore, IVOCs in mobile-source emissions contribute almost as much SOA as traditional precursors such as single-ring aromatics. However, accounting for these emissions in CMAQ does not reproduce measurements of either ambient SOA or IVOCs. To investigate the potential contribution of other IVOC sources, we performed two exploratory simulations with varying amounts of IVOC emissions from nonmobile sources. To close the mass balance of primary hydrocarbon IVOCs, IVOCs would need to account for 12% of NMOG emissions from nonmobile sources (or equivalently 30.7 t d-1 in the Los Angeles-Pasadena region), a value that is well within the reported range of IVOC content from volatile chemical products. To close the SOA mass balance and also explain the mildly oxygenated IVOCs in Pasadena, an additional 14.8% of nonmobile-source NMOG emissions would need to be IVOCs (assuming SOA yields from the mobile IVOCs apply to nonmobile IVOCs). However, an IVOC-to-NMOG ratio of 26.8% (or equivalently 68.5 t d-1 in the Los Angeles-Pasadena region) for nonmobile sources is likely unrealistically high. Our results highlight the important contribution of IVOCs to SOA production in the Los Angeles region but underscore that other uncertainties must be addressed (multigenerational aging, aqueous chemistry and vapor wall losses) to close the SOA mass balance. This research also highlights the effectiveness of regulations to reduce mobile-source emissions, which have in turn increased the relative importance of other sources, such as volatile chemical products.

Preparation of ion-imprinted montmorillonite nanosheets/chitosan gel beads for selective recovery of Cu(â ¡) from wastewater.

The novel ion-imprinted montmorillonite nanosheets/chitosan (IIMNC) gel beads were prepared for selective adsorption of Cu2+. The IIMNC gel beads were characterized by scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The results showed that IIMNC was successfully assembled and rich in honeycombed pores, which performed well in the removal of Cu2+ through the synergistic effect of montmorillonite nanosheets and chitosan. The elimination of copper was followed by pseudo-second-order model and was enhanced by introduced montmorillonite nanosheets (MMTNS) because MMTNS attracted Cu(Ⅱ) by its negative charge and provided active adsorption sites through its high performance of cation exchange. This composite gel also showed excellent reusability, performing well in the removal of Cu2+ after undergoing adsorption-desorption in five cycles, because the adsorption sites of MMTNS can be continually reactivated by NaOH solution. More importantly, its high selectivity for Cu2+ provides a feasible way to recover Cu2+ from wastewater containing various cations.

Adsorption toward Cu(II) and inhibitory effect on bacterial growth occurring on molybdenum disulfide-montmorillonite hydrogel surface.

Novel molybdenum disulfide-montmorillonite (MoS2@2DMMT) hydrogels for Cu(II) removal and inhibition on bacterial growth were successfully prepared. MoS2 was first in-situ growth onto 2DMMT platelet through hydrothermal method and then cross-linked with organic reagents to form hydrogels. The flower-like structure of synthesized MoS2 could be clearly observed in MoS2@2DMMT by SEM. The synthesized hydrogels possessed a three-dimensional macroporous structure, offering a free access for contaminants to get inside and combine with the active sites. Adsorption tests revealed that efficient Cu(II) removal (65.75 mg/g) could be achieved within a short time (30 min) at pH 5. The pseudo-second-order kinetics model and Langmuir isotherm model indicated the existence of chemisorption and monolayer absorption for Cu(II) onto MoS2@2DMMT hydrogels. Characterizations of EDS and XPS indicated that Cu(II) reacted with groups of carboxyl, hydroxyl and amidogen. Bacteriostatic tests revealed that almost a complete bacteriostatic was achieved with just small dosage (0.8 mg/mL) of MoS2@2DMMT hydrogels after the Cu(II) removal under the normal illumination. The mechanism was ascribed to the destructive effect of Cu(II) to the cytomembrane and the damage of reactive oxygen species (ROS) to the DNA. Such hydrogel not only provided insights for treating co-existing contaminates, but also guides for designing novel polymer materials from two-dimensional (2D) nano-materials.

Selective recovery of heavy metals from wastewater by mechanically activated calcium carbonate: Inspiration from nature.

In nature, the calcium carbonate shows different interactions with different metal ions. Inspiration from this natural phenomenon, in this work, the selective recovery of heavy metals from wastewater by mechanically activated calcium carbonate was investigated. The changes in Ca2+ concentration, pH value and metals uptake ratio of solution showed that M2+ (M = Cu, Mn, Zn and Ni) were endowed with different migration rules, resulting in the various interaction with the calcium carbonate in metal-bearing solution. The combination of XRD, SEM, and stereomicroscope affirmed that the adsorbed M2+ rarely change the lattice structure of calcium carbonate, while the adsorbed Cu2+ and Zn2+ could convert the mineral phase from calcium carbonate to posnjakite and hydrozincite, respectively. As a result of phase transition, 15% Cu2+ and 6% Zn2+ were uptaken with initial concentration of 1 mM for 100 min, however, the unsatisfactory recovery prevented the efficient recycling of metal. The mechanically activated calcium carbonate had a superior solubility at the solid/liquid interface, promoting mineral phase transformation on the premise of weak displacement adsorption. Hence, the uptake ratio of Cu2+ and Zn2+ were significantly increased to 99% and 53% at the same condition. Finally, Cu2+ was recovered from polymetallic systems from complex environment with high precision. The concept of selective recycling in this research guides the development of innovative processes from natural information.

Enhanced removal of methyl orange on exfoliated montmorillonite/chitosan gel in presence of methylene blue.

In this work, self-assembled gels were prepared with exfoliated montmorillonite and chitosan (EMCG) as the adsorbent for removing methyl orange (MO) from water in absence and presence of methylene blue (MB). Several techniques including scanning electron microscope (SEM), zeta potential, fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) were used for the characterization of the EMCG before and after removal of MO. The EMCG performed well in the removal of MO attributing to the electrostatic attraction, cation exchange and hydrogen bond. The adsorption behaviors were followed pseudo-second-order and Langmuir isotherm. More surprisingly, the maximum adsorption capacity of MO was obviously enhanced in the presence of MB that it increased from 545 mg g-1 (absence of MB) to 1060 mg g-1 with the shielding effect of MB on EMCG which allowed MO and MB to alternately arrange at the adsorption sites. This finding of the synergistic effect between the two dyes on the proposed composite opens up new vistas to imagine the enhanced purification of the wastewater with multiple dyes co-existed using the multifunctional adsorbents.

Utilization of carbonate-based tailings to remove Pb(II) from wastewater through mechanical activation.

The removal of lead in water and disposal of tailings are important environmental issues that need to be addressed urgently. This work explored the feasibility of utilizing the carbonate-based tailings (CBT) for removing lead from the simulated wastewater with the aid of wet stirred ball milling (mechanical activation). Batch experiments were performed to evaluate the influences of various experimental parameters like dosage of CBT, milling balls addition and initial concentration of lead. Under the action of mechanical activated CBT, the lead removal in the solution could reach more than 99% in 2 h, and the lead removal capacity reached 832 mg/g. The results of X-Ray Diffraction (XRD), Fourier Transform infrared spectroscopy (FTIR) and Scanning Electron Microscope-Energy Dispersive Spectra (SEM-EDS) revealed that the calcite (CaCO3) in CBT played a major role in removing lead and the lead in the solution was transferred to the precipitate as cerussite (PbCO3). The mechanical activation promoted the dissolution of calcite, reduced the particle size of CBT and peeled off the lead carbonate precipitation on the surface of calcite, thereby enabling the reaction to be efficiently and thoroughly completed. The lead content in the precipitate after the reaction reached 38.4 wt%, which made it possible for lead recovery.

High-performance two-dimensional montmorillonite supported-poly(acrylamide-co-acrylic acid) hydrogel for dye removal.

High-performance two-dimensional montmorillonite supported-poly (acrylamide-co-acrylic acid) hydrogel for dye removal was investigated. Montmorillonite cooperated with acrylamide and acrylic acid via polymerization, hydrogen-bond, amidation and electrostatic interactions to form the three-dimensional reticular-structured hydrogel with the free entrance for macromolecules. Adsorption tests revealed that the efficient removal (97%) for methylene blue at high concentration (200 mg/L) could be achieved via a small dose of hydrogel (0.5 g/L) within a short time (20 min). The excellent adsorption performance was profited from the electronegative surface and fully exposed reaction sites of two-dimensional montmorillonite, which could save the treatment cost and promote the removal effect compared with the conventional adsorbents. The adsorption process of methylene blue onto hydrogel could be fitted by both the pseudo-first-order and pseudo-second-order kinetics models, and the adsorption isotherm corresponded to the Sips model. The mechanism analysis based on Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy measurements illustrated that the reaction between carboxyl groups and methylene blue molecules as well as the cation-exchange enabled the hydrogel performing extraordinary adsorption efficiency.

Removal of Cu(II) from wastewater by using mechanochemically activated carbonate-based tailings through chemical precipitation.

This work explored the feasibility of utilizing the copper tailings (CT) for removing copper from the waste mine water based on the mechanochemical activation. Batch experiments were performed to evaluate the influences of various experimental parameters like the dosage of CT, reaction time, initial concentration of Cu, and anion species. By cogriding copper solution with CT in the stirred mill (mechanochemical activation), over 99.5% of copper was removed and the residual copper concentration in the solution was less than 0.5 mg/L, reaching the discharge limit. This reaction was a chemical precipitation process. The calcite of CT played a major role in precipitating copper and had a better removal effect on copper in the copper sulfate solution than copper nitrate solution. For copper sulfate solution, the copper deposit was mainly posnjakite (Cu4(SO4)(OH)6·H2O). In the copper nitrate solution, the copper sediment might consist mainly of basic copper nitrate. The stability of the two reaction products was measured by leaching test. The result showed that the sediment obtained by this method was relatively stable and was not hazardous wastes.

Synthesis of chitosan cross-linked 3D network-structured hydrogel for methylene blue removal.

TiO2 loaded 2D montmorillonite (2DMMT)-chitosan-poly (acrylic acid) hydrogel with 3D network structure as a novel adsorbent for methylene blue (MB) removal was investigated. The hydrogel was formed via the polymerization and molecular forces between 2DMMT and polysaccharide. Physicochemical analysis and factor experiments were implemented on hydrogel. The results implied that hydrogel possessed a porous structure and high surface area, facilitating the access and removal of MB. A completely removal of MB could be achieved in a small hydrogel dose of 0.2 g/L within 120 min even after 5 regeneration cycles, which could lower costs and enhance efficiency dramatically. MB adsorption onto hydrogel was reasonably correlated with pseudo-second-order kinetic model and Redlich-Peterson isotherm model. MB adsorption mechanism onto hydrogel was analyzed by FTIR, EDS and XPS. It was found MB molecules reacted with carboxyl groups as well as substituted cation from 2DMMT. Such hydrogel could not only realize the green/sustainable application in water treatment, but also guide the preparation for polymer materials from polyelectrolyte and nanoclay.