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Some of conventional wastewater disinfectants can have a harmful influence on the environment as well as human health. The aim of this investigation was synthesis and characterizes ecofriendly pectin/hydroxyethyl cellulose (HEC)/clay and pectin/HEC/clay incorporated with titanium dioxide nanoparticles (TiO 2 NPs) and use the prepared bionanocomposite as microbial disinfectants for real wastewater. Pectin/HEC/clay and pectin/HEC/clay/TiO 2 bionanocomposite were characterized by various methods including X-ray diffraction (XRD), scanning electron microscope (SEM), and Fourier-transform infrared spectroscopy (FTIR), thermal gravimetric analysis (TGA). Mechanical properties and water vapor permeability (WVP) were carried out. The results of SEM showed that, the prepared bionanocomposite had a smooth surface. Additionally, TiO 2 nanoparticles to the pectin/HEC/clay composites may lead to changes in the FTIR spectrum. The intensity of XRD peaks indicated that, TiO 2 NPs was small size crystallite. TGA illustrated that pectin has moderate thermal stability, while HEC generally exhibits good thermal stability. The TEM showed that, TiO 2 nanoparticles have diameters <25 nm. On the other hand, antimicrobial activities of pectin/HEC/clay against Escherichia coli (E. coli), Staphylococcus aureus and Candida albicans have been enhanced by adding TiO 2 NPs. The minimum inhibitory concentration (MIC) of pectin/HEC/clay/TiO 2 against E. coli was 200 mg/mL. Moreover, complete eradication of E. coli, Salmonella and Candida spp. from real wastewater was observed by using pectin/HEC/clay/TiO 2 bionanocomposite. Finally, it can be concluded that, the synthesized bionanocomposite is environmentally friendly and considered an excellent disinfectant matter for removal of the microbial pathogens from wastewater to safely reuse., Competing Interests: Declaration of competing interest The authors hereby declare that the disclosed information is correct and that no other situation of real, potential or apparent conflict of interests., (Copyright © 2024 Elsevier B.V. All rights reserved.)

Waterborne pathogens threaten 2.2 billion people lacking access to safely managed drinking water services, causing over a million annual diarrheal deaths. Individuals without access to chlorine reagents or filtration devices often resort to do-it-yourself (DIY) methods, such as boiling or solar disinfection (SODIS). However, these methods are not simple to implement. In this study, we introduced an innovative and easily implemented disinfection approach. We discovered that immersing aluminum foil in various alkaline solutions produces alkali-treated aluminum foil (ATA foil) that effectively adsorbs Escherichia coli (E. coli), Salmonella, and Acinetobacter through the generated surface aluminum hydroxide. For example, a 25 cm 2 ATA foil efficiently captures all 10 4 E. coli DH5α strains in 100 mL water within 30 min. Using a saturated suspension of magnesium hydroxide, a type of fertilizer, as the alkaline solution, the properties of the saturated suspension eliminate the need for measuring reagents or changing solutions, making it easy for anyone to create ATA foil. ATA foils can be conveniently produced within mesh bags and placed in household water containers, reducing the risk of recontamination. Replacing the ATA foil with a foil improves the adsorption efficiency, and re-immersing the used foil in the production suspension restores its adsorption capacity. Consequently, ATA foil is an accessible and user-friendly alternative DIY method for underserved communities. Verification experiments covering variations in the water quality and climate are crucial for validating the efficacy of the foil. Fortunately, the ATA foil, with DIY characteristics similar to those of boiling and SODIS, is well-suited for testing under diverse global conditions, offering a promising solution for addressing waterborne pathogens worldwide., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier B.V.)

The forward osmosis (FO) process has recently gained significant interest in treating wastewater, brackish/seawater and concentrating feedstocks for various operations, including desalination. The study investigates the effect of different synthesis conditions of the polyamide-based thin-film composite (TFC) FO membranes on the membranes' final performance. Taguchi statistical analyses were used to fabricate and optimize the polyamide TFC FO membrane. The process parameters as factors were the amount of polyethersulfone (PES), polyethylene glycol 400 (PEG-400), polyvinyl pyrrolidone (PVP), m-phenylenediamine (MPD), and trimesoyl chloride (TMC), and TMC reaction-time (RT). The Taguchi method was adopted to investigate the optimal conditions and the significance of individual factors using an L16 (4 5 ) orthogonal array. Another Taguchi analysis (Taguchi 2) was adopted to investigate the influence of other important parameters like optimal conditions for MPD, TMC, and TMC reaction-time factors using an L9 (3 3 ) orthogonal array. Confirmation tests validated a maximum water flux of 46.4 ± 2.32 L/m 2 ·h with a specific combination of control factors for membrane synthesis: PES/PEG/PVP/MPD/TMC/TMC RT-16/7/0.5/1/0.05/30. These tests demonstrated a high-water flux of 7.05 ± 0.35 L/m 2 ·h when exposed to industrial wastewater (secondary effluent) as the feed solution (FS) and fertilizer as the draw solution (DS) in the FO process. The R 2 values were more than 90%. The experimental validation confirmed the models' predictive ability with different FSs, including industrial wastewater., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Microplastics (MPs), as emerging pollutants, have attracted the attention of environmentalists, statespersons, and the scientific community over the last few decades. To address the spread of MPs in the environment, it is imperative to develop various removal techniques and materials that are effective, scalable, and ecologically benign. However, to the best of our knowledge, no review has systematically examined the removal of MPs using adsorption or provided an in-depth discussion on various adsorbents. Adsorption is an inexpensive and effective technology for wastewater treatment. Recently, many researchers have conducted studies on MP remediation using diverse adsorbent materials, such as biochar, activated carbon, sponges, carbon nanotubes, metal-layered oxides, metal-organic frameworks (MOFs), and zeolites. Each adsorbent has advantages and disadvantages. To overcome their disadvantages, researchers have been designing and developing hybrid adsorbents for MP remediation. This review provides insights into these individual adsorbents and also discusses hybrid adsorbents for MP removal. Finally, the review elaborates on future possibilities and ways to enable more efficient, scalable, and environmentally friendly MP cleanup. Overall, this review bridges the gap between contemporary MP remediation using adsorption techniques and adsorbent development., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Ltd.)

The heavy metals, pesticides and dyes in agriculture and industry caused serious water pollution have increased the urgency for the advancement of biomass-based adsorbents due to their merits of low cost, high efficiency, and environmental sustainability. Thus, this review systematically examines the recent progress of lignin-based adsorbents dedicated to wastewater purification. Commencing with a succinct exposition on the intricate structure and prevalent forms of lignin, the review proceeds to expound rational design strategies tailored for lignin-based adsorbents coupled with adsorption mechanisms and regeneration methods. Emphasis is placed on the potential industrial applications of lignin-based adsorbents, accentuating their capacity for recovery and direct utilization post-use. The future challenges and outlooks associated with lignin-based adsorbents are discussed to provide novel perspectives for the development of high-performance and sustainable biosorbents, facilitating the effective removal of pollutants and the value-added utilization of resources in a sustainable manner., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Ltd.)

In modern times, wastewater treatment is vital due to increased water contamination arising from pollutants such as nutrients, pathogens, heavy metals, and pharmaceutical residues. Polysaccharides (PSAs) are natural, renewable, and non-toxic biopolymers used in wastewater treatment in the field of gas separation, liquid filtration, adsorption processes, pervaporation, and proton exchange membranes. Since addition of nanoparticles to PSAs improves their sustainability and strength, nanocomposite PSAs has gained significant attention for wastewater treatment in the past decade. This review presents a comprehensive analysis of PSA-based nanocomposites used for efficient wastewater treatment, focusing on adsorption, photocatalysis, and membrane-based methods. It also discusses potential future applications, challenges, and opportunities in adsorption, filtration, and photocatalysis. Recently, PSAs have shown promise as adsorbents in biological-based systems, effectively removing heavy metals that could hinder microbial activity. Cellulose-mediated adsorbents have successfully removed various pollutants from wastewater, including heavy metals, dyes, oil, organic solvents, pesticides, and pharmaceutical residues. Thus, PSA nanocomposites would support biological processes in wastewater treatment plants. A major concern is the discharge of antibiotic wastes from pharmaceutical industries, posing significant environmental and health risks. PSA-mediated bio-adsorbents, like clay polymeric nanocomposite hydrogel beads, efficiently remove antibiotics from wastewater, ensuring water quality and ecosystem balance. The successful use of PSA-mediated bio-adsorbents in wastewater treatment depends on ongoing research to optimize their application and evaluate their potential environmental impacts. Implementing these eco-friendly adsorbents on a large scale holds great promise in significantly reducing water pollution, safeguarding ecosystems, and protecting human health., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

Electrospinning nanofibers membrane has received much attention to remove the insoluble oil from the sewage, while the poor mechanical strength and low oil/water separation efficiency of membranes limit their practical application. Here, we prepared a superwettable deacetylated cellulose acetate (d-CA)-based electrospinning nanofibers membrane simply dipped by bacterial cellulose (BC) and cross-linked with citric acid (CCA) to construct the spider-web structure spontaneously. Compared with the pristine d-CA membrane, the obtained d-CA/BC@CCA membrane exhibits the remarkable oil/water separation performance. The flux and separation efficiency of n-hexane/water emulsion without (SFE) and with (SSE) emulsifier for d-CA/BC@CCA membrane are 9364 L·m -2 ·h -1 ·bar -1 , 98.34 % and 5479 L·m -2 ·h -1 ·bar -1 , 99.39 %, respectively, which are mainly attributed to the improved hydrophilicity of its surface and the decreased pore sizes caused by the unique spider-web structure. In addition, d-CA/BC@CCA membrane also possesses the outstanding mechanical properties, the better cycle stability, as well as the excellent durability. This study provides a novel strategy for the construction of the high-performance oil/water separation membrane., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Flocculation is a common process for wastewater treatment. However, the most commonly used organic synthetic flocculants such as polyacrylamide are petroleum-based. In this work, biomass lignin was grafted with cationic starch to synthesize low-cost, green and fully biomass-based multifunctional flocculants. The cationic polyacrylamide was replaced by cheap industrial cationic starch. Hyperbranched multifunctional lignin-grafted cationic starch flocculant (CS-L) was successfully prepared via ring-opening reaction with epichlorohydrin. The mass content of lignin in the grafted product was between 16.6 % and 70.1 %. With the dosage of CS-L between 4.0 and 7.5 mg/l, the turbidity removal rate for 500 mg/l kaolin suspension reached more than 97 %. When the dosage of CS-L was 24 mg/l, the removal rate of 50 mg/l Cu 2+ reached 85.7 %. Importantly, when the mixed solution of kaolin particles and Cu 2+ was treated, the synchronous removal rates of kaolin and Cu 2+ reached 90 % and 72 % respectively in the range of 8.0-12.0 mg/l flocculant addition. The synthesized lignin-grafted cationic starch flocculant showed an excellent multifunctional flocculation function., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Hypothesis: Super-hydrophilic/underwater super-oleophobic materials composed of biomass show great advantages for the treatment of oily wastewater due to their inherent fouling resistance. However, the development of three-dimensional materials from biomass for oil-water separation is still a challenge. It is universally acknowledged that constructing a rough structure on the surface of hydrophilic substrates would significantly improve the underwater oleophobicity and oil-water separation performance., Experiments: In this work, a three-dimensional lignin/cellulose aerogel (LCA) was developed through sol-gel method with freeze-drying. The rough microstructure and 3D interconnected network composed of lignin and cellulose impart excellent underwater superoleophobicity to LCA for efficient oil-water separation., Findings: The introduction of lignin to cellulose aerogel could effectively enhance its surface roughness, water permeation speed and underwater oil contact angle. Especially, the swelling properties of the hydrogel could be regulated by modulating the content of lignin, which could further control the pore size of aerogels to optimize the separation flux. The as-prepared aerogel showed remarkable performance in separating various oil-water mixtures and oil-in-water emulsions, with a separation flux of 7646 ± 167 L·m -2 ·h -1 and oil rejection rate >99 %. These excellent properties combined with its facile fabrication make LCA a promising candidate for the treatment of oily wastewater., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

The study analyzed the potential of leaf powder prepared from the residual leaves of the species Sansevieria trifasciata, as a potential adsorbent for methylene blue (MB) removal. The equilibrium was reached fast for almost all concentrations after 60 min, obtaining the maximum capacity of 139.98 mg g -1 for 200 mg L -1 . The increase in temperature disfavored the dye adsorption, with the maximum adsorption capacity of 225.8 mg g -1 , observed for 298 K. The thermodynamic parameters confirmed that the adsorption process is spontaneous and exothermic. A direct sloping curve was established for the fixed bed, with breakthrough time (t b ), column stoichiometric capacities (q eq ), and the mass transfer zone lengths (Z m ) were 1430, 1130, and 525 min; 60.48, 187.01, and 322.65 mg g -1 ; and 8.81, 11.28, and 10.71 cm, for 100, 200, and 500 mg L -1 , respectively. Furthermore, in a mixture of several dyes, the adsorbent obtained the removal of 51% of the color., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Amoxicillin (AMX) is a widely used antibiotic, which induces harmful effects to nature via bioaccumulation and persistence in the environment if discharged untreated into water bodies. In the current study, a novel bionanocomposite, bismuth oxyiodide-chitosan (BiOI-Ch), was synthesized by a facile precipitation method and its amoxicillin (AMX) adsorption capacity in the presence of ultrasonic waves has been explored. Multiple batch experiments were performed to achieve the optimum operational parameters for maximum adsorption of AMX and the obtained results were as follows: pH 3, 80 mg g -1 AMX concentration, 1.7 g L -1 adsorbent dose, temperature 298 K and ultrasonication time 20 min. Composite removed approximately 90% AMX from the solution under optimized conditions, while the maximal adsorption capacity was determined to be 81.01 mg g -1 . BiOI-Ch exhibited superior adsorption capacity as compared to pure BiOI (33.78 mg g -1 ). To understand the dynamics of reaction, several kinetic and isotherm models were also examined. The adsorption process obeyed pseudo-second-order kinetic model (R 2  = 0.98) and was well fitted to Freundlich isotherm (R 2  = 0.99). The addition of biowaste chitosan to non-toxic bismuth-based nanoparticles coupled with ultrasonication led to enhanced functional groups as well as surface area of the nanocomposite resulting in superior adsorption capacity, fast adsorption kinetics and improved mass transfer for the removal of AMX molecules. Thus, this study demonstrates the synergistic effect of ultrasonication in improved performance of novel BiOI-Ch for potential application in the elimination of persistent and detrimental pollutants from industrial effluent after necessary optimization for large-scale operation., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Nanocellulose hydrogels are promising sustainable biosorbents for removing heavy metal ions for wastewater treatment. However, the nanocellulose hydrogels reported thus far typically suffer from inferior adsorption performance and/or poor mechanical stability, thus limiting their industrial applications. Achieving the goals of mechanical stability and high removal capability remains a crucial technical challenge, which may be addressed, as presented in this study, by developing novel core-shell carboxymethylated cellulose nanofibril (CMCNF)/sodium alginate (SA) hydrogel beads (CAbs). By immobilizing CMCNFs (shell) on the surface of the SA hydrogel bead (core) via electrostatic attractions and hydrogen bonding, a mechanically stable hydrogel bead with a core-shell configuration was constructed, which shows a Cu(II) removal capacity of up to 221 mg/g that exceeds that of CMCNFs and most other nanocellulose structural adsorbents. Furthermore, both the formation principle of the core-shell structure and the Cu(II) removal mechanism were explored in detail. Finally, we demonstrated a potential application of core-shell CAbs to treat drinking water with a low concentration of Cu(II) using a homemade column adsorption device. This work brings sustainable nanocellulose adsorbents a step closer to industrial applications for Cu(II) wastewater treatment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Coating manufacturing, textile processing, and plastic industry have led to dramatical release levels of hazardous organic dye pollutants threatening public health and the environment. To solve this problem, porous carbon materials are being developed following with the United Nations initiative on water purification. However, conventional porous carbon materials face many challenges, such as limited removal rates, low adsorption capacity, and high chemicals consumption, hampering their large-scale utilization in dye wastewater treatment. Herein, we demonstrate a high-performance lignin-derived hierarchical porous carbon (LHPC) material directly prepared from renewable lignin through a low-cost activation procedure. The large specific surface area (1824 m 2 /g) enables the rapid and effective adsorption of organic dyes. Therefore, the LHPC exhibits an ultrahigh adsorption ability (1980.63 mg/g) and removal rate (99.03% in 10 min) for Azure B, superior to that of other adsorbents. Additionally, the LHPC adsorbent, organic dyes, eluting agent, and water all can be recycled and reused in a designed close-looped system. Its high removal ability and rate, strong retrievability, low-cost and scalable production combined with high dyes adsorption universality, positions our LHPC as a promising commercial adsorbent candidate for the purification of harmful organic dye wastewater, especially for heavily polluted area with an insistent demand for clear water., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Solar-driven interfacial evaporation has enormous promise for fresh water recovery and salt harvesting, but salt accumulation-related challenges stand in its way. Herein, we report a spined groove-ridge pairs inspired by the shell ornamentation of the Vasticardium vertebratum, which addresses salt accumulation by artfully integrating salt reflux into localized salt crystallization. The seashell-mimetic radial V-groove array enables the 3D evaporator to transport water rapidly and directionally, resulting in high-performance water evaporation (∼95% efficiency) and localized crystallization. The periodic spines enlightened by the spine-bearing ridge on the seashell provide considerable micro-unit salt reflux. The 2-in-1 integration design endows the three-dimensional evaporator with superior solar-driven zero liquid discharge and excellent long-term salt resistance even when dealing with high-salinity brine (20 wt% NaCl) and a series of heavy metallic salt solutions. Our design offers a new alternative solution to avoiding salt scaling and could advance locally crystallized solar evaporators towards practical applications., Competing Interests: Declaration of Competing Interest The authors declare no competing interest., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Developing new and efficient technologies for environmental remediation is becoming significant due to the increase in global concerns such as climate change, severe epidemics, and energy crises. Air pollution, primarily due to increased levels of H 2 S, SO x , NH 3 , NO x , CO, volatile organic compounds (VOC), and particulate matter (PM) in the atmosphere, has a significant impact on public health, and exhaust gases harm the natural sulfur, nitrogen, and carbon cycles. Similarly, wastewater discharged to the environment with metal ions, herbicides, pharmaceuticals, personal care products, dyes, and aromatics/organic compounds is a risk for health since it may lead to an outbreak of waterborne pathogens and increase the exposure to endocrine-disrupting agents. Therefore, developing new and efficient air and water quality management systems is critical. Metal-organic frameworks (MOFs) are novel materials for which the main application areas include gas storage and separation, water harvesting from the atmosphere, chemical sensing, power storage, drug delivery, and food preservation. Due to their versatile structural motifs that can be modified during synthesis, MOFs also have a great promise for green applications including air and water pollution remediation. The motivation to use MOFs for environmental applications prompted the modification of their structures via the addition of metal and functional groups, as well as the creation of heterostructures by mixing MOFs with other nanomaterials, to effectively remove hazardous contaminants from wastewater and the atmosphere. In this review, we focus on the state-of-the-art environmental applications of MOFs, particularly for water treatment and air pollution, by highlighting the groundbreaking studies in which MOFs have been used as adsorbents, membranes, and photocatalysts for the abatement of air and water pollution. We finally address the opportunities and challenges for the environmental applications of MOFs., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Solar-driven steam generation for desalination is a facile, sustainable, and energy-saving approach to produce clean freshwater. However, the complicated fabrication process, high cost, potential environmental impact, and salt crystallization of conventional evaporators limit their large-scale application. Herein, we present a sustainable Janus evaporator based on a biopolymer sponge from the water hyacinth petiole (WHP) for high-performance solar steam generation. The freeze-dried WHP maintained its original porous structure and aligned channels well, and therefore holds the capability for rapid water transport due to strong capillary action. The WHP coated with carbon nanotubes/ethyl cellulose paste on its surface (WHP-C) gains a good photothermal property, thus achieving an efficient solar steam generation with a rate of 1.50 kg m -2 h -1 under 1 sun irradiation. Moreover, the WHP-C after hydrophobic modification by fluorocarbon (WHP-CH) is endowed with high water repellency and exhibits good salt resistance during long-term solar desalination. Additionally, we demonstrate that a stable wet surface that enables efficient water supply and vapor escape is also significant to the successive desalination of a solar evaporator. Our work provides new insights into the high-value utilization of biomass waste, i.e., water hyacinth, and the development of sustainable interfacial solar evaporators for the environmentally friendly production of freshwater.

Water is a valuable natural resource, which plays a crucial role in ecological survival as well as economic progress. However, the water quality has deteriorated in recent years as a result of urbanization, industrialization and human activities due to the uncontrolled release of industrial wastes, which can be extremely carcinogenic and non-degradable, in air, water and soil bodies. Such wastes showed the presence of organic and inorganic pollutants in high dosages. Heavy metals are the most obstinate contaminants, and they can be harmful because of having a variety of detrimental consequences to the ecosystem. The existing water treatment methods in many situations may not be sustainable or effective because of their high energy requirements and ecological impacts. In this review, state-of-the-art water treatment methods for the elimination of heavy metals with the help of protein nanofibrils are covered featuring a discussion on the strategies and possibilities of developing protein nanofibrils for the active elimination of heavy metals using kitchen waste as well as residues from the cattle, agriculture, and dairy industries. Further, the emphasis has been given to their environmental sustainability and economical aspects are also discussed., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Over the previous three decades, the worldwide use of pharmaceuticals has surged by more than 2.5 times. Although being considered essential to save many lives, pharmaceuticals have also emerged as a large source of complex environmental contaminants in recent decades. Consequently, the pharmaceuticals and their breakdown products are ending up into the water bodies thus progressively contaminating them and the surrounding environments. Based on recent studies concentrations in water sources are typically >0.1 μg/l and the concentration in treated water is typically >0.05 μg/l. These pharma drugs are removed from aquatic systems by processes such as oxidation, Ultraviolet degradation, reverse osmosis and nano-filtration. However, hazardous sludge creation, incomplete removal, expensive capital and operating costs, and the need for professional operating and maintenance personnel have all limited the economic sustainability of these systems. As a result, the presence of pharmaceuticals in water necessitates even more advanced technologies of purification to harvest clean water, yet present approaches are constrained by their high costs, low reusability, and disposal issues. Here, we review sustainable adsorbents for the removal of pharmaceuticals from wastewater. In this comprehensive review, an evaluation of water contamination caused by pharmaceutical compounds is discussed. An overview of current research on the employment of sustainable adsorbents for the removal of the major pharmaceuticals prevalent in water sources. Numerous aspects of high adsorption efficiencies of these pharmaceutical compounds with such sustainable adsorbents were observed; however, other factors, such as adsorbent regeneration and cost evaluation, must be taken into account in order to assess the true applicability of adsorbents., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The rapid and efficient treatment of complex wastewater remains challenging. Herein, green paper-based materials with high wet strength, good oil-water separation property and high heavy metal ion adsorption capacity were prepared via a facile, cost-effective process. The introduction of amphoteric functional groups not only met the requirements for heavy metal ion adsorption, but also maintained the stable underwater superoleophobic properties of materials a wide pH range. The covalent crosslinking between cellulose fibers induced by polyethyleneimine and citric acid significantly improved the wet strength (up to 26.0 Nm/g) and the porosity. The membrane flux was increased up to 3515 L/(m 2 ·h) and the separation efficiencies were higher than 98%. Moreover, the theoretical maximum adsorption capacities for Cd(II) and Pb(II) reached 73.29 and 93.75 mg/g, respectively. Combined with filtration technology, the materials can realize the continuous and efficient purification of complex wastewater., (Copyright © 2022. Published by Elsevier B.V.)

Cold caustic extraction (i.e. CCE) is an essential technique for removing hemicellulose from paper-grade pulp and thus obtaining high-purity dissolving pulp in pulp and paper industry. The generated wastewater from the CCE process contains large amounts of valuable hemicellulose which should be properly treated in a cost-effective way. Therefore, in this research, the hemicellulose has been used as a raw material for preparing hemicellulose-graft-polyacrylamide (hemi-g-pAAm) hydrogel particles for efficiently adsorbing methylene blue (MB) from aqueous solutions. The mass transfer kinetic behaviours of hemicellulose during a multiple CCE process were also studied. The MB adsorption kinetic test results showed that the removal efficiency can be higher than 90% for the simulated wastewater containing 500 mg/L of MB. Of note, the maximum removal capacities for the wastewater samples containing 500 and 1000 mg/L of MB could be reached up to ∼1800 and ∼2300 (mg/g) respectively with the equilibrium time of ∼40 min. Compared to other reported materials, the superior adsorption performance of the prepared hemicellulose-based hydrogel proved its great potential for application in the wastewater treatment of dye industry.

Developing a sustainable, efficient and recyclable heterogeneous Fenton-like catalyst is important to wastewater treatment. Herein, well-dispersed MnO 2 and Fe 3 O 4 nanoparticles inlaid in chitosan beads (MnO 2 -Fe 3 O 4 /CH) was firstly fabricated and employed in the degradation of methylene blue (MB). The bead was prepared via a facile one-step method by dropwise addition of chitosan-metal salt solution into alkaline solution. Comparing with monometallic chitosan beads (MnO 2 /CH, Fe 3 O 4 /CH) and naked MnO 2 -Fe 3 O 4 , MnO 2 -Fe 3 O 4 /CH displayed significantly higher activity for MB degradation with the assistance of hydrogen peroxide (H 2 O 2 ), finally removing 96.8% MB under the optimal conditions (50 mg L -1  MB, 4.0 g L -1 catalyst, 30 g L -1 H 2 O 2 , pH = 7, 60 min). Based on a series of characterizations, the large surface area (60.1 m 2  g -1 ), well-developed porosity (0.3 cm 3  g -1 ), and intensified electron transport of MnO 2 -Fe 3 O 4 /CH consequently enhanced the catalytic performance via a synergistic effect. Because the specific porous structure of MnO 2 -Fe 3 O 4 /CH facilitated the adsorption/diffusion of reactants and exposure of active sites. Meanwhile, the electron transfer from Mn 3+ to Fe 3+ accelerated the Fe 3+ /Fe 2+ cycle, which favored the production of dominant reactive species hydroxyl radical for MB degradation. Besides, the magnetic beads could be easily collected from the solution and reused for five times with a negligible leaching., (Copyright © 2021 Elsevier B.V. All rights reserved.)

It is expected that low-energy and scientific zero discharge of chemical-mechanical pulping wastewater will be achieved by applying the mechanical vapor recompression (MVR) technology. In this paper, the equal-standard pollution load model was introduced into pulp and paper field to parse the pollution sources for the first time. The results from the source apportionment indicated that the screw press and concentrating were the major pollution unit operations, and their cumulative load ratio reached 92.92%. The further survey demonstrated that the dominating pollution factors in the traditional chemical-mechanical pulping process were Chemical Oxygen Demand (COD), Biochemical Oxygen Demand (BOD 5 ), and Suspended Solids (SS), whose cumulative load ratio was 92.69%. The environmental analysis demonstrated the implementation of MVR technology significantly decreased the pollution load and reduce the pressure of subsequent wastewater treatment. In addition, a further economic performance indicated that the utilization of MVR technology possessed a smaller operating cost of 2.899 $/m 3 . The result of the given model provides a scientific gist and instruction for the future treatment of water pollutants in the chemical-mechanical pulping process. The MVR technology is conducive for wastewater treatment to minimize environmental effects and costs., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Advanced oxidation processes (AOPs) based on persulfate (PS) has attracted great attention due to its high efficiency for degradation of organic pollutants. Manganese-based materials have been considered as the desirable catalysts for in-situ chemical oxidation since they are abundant in the earth's crust and environment-friendly. In this study, manganese oxyhydroxide (MnOOH) was used as an activator for PS to degrade p-chloroaniline (PCA) from wastewater. The effects of MnOOH dosage, PS dosage and initial pH on PCA degradation performance were studied. Experimental results showed that PCA degradation efficiency was enhanced by higher MnOOH and PS addition, and the degradation efficiency was slightly inhibited as the initial pH increased from 3 to 9. MnOOH showed excellent stability and reusability when used as the activator of PS. In addition, a comprehensive study was conducted to determine the PS activation mechanism. The results revealed that PS activation by MnOOH followed a nonradical mechanism. No 1 O 2 was generated, and the main active substance in the reaction was the activated PS molecule on the surface of MnOOH. The hydroxyl group on the catalyst surface acted as a bridge connecting PS and the catalyst, leading to the activation of PS. The intermediates during PCA degradation were also analyzed, and three possible degradation pathways of PCA were proposed. This study expects to deepen the understanding of the PS activation mechanism by manganese oxide, and provides technical support for the practical application of AOPs of manganese-based materials for wastewater treatment., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Hydrodynamic cavitation treatment was used for the functional inactivation of quorum-sensing lactone molecules of Pseudomonas aeruginosa. Hydroxyl radicals formed as well as the shear effects during the cavitation process induced the inactivation of the signal molecules through hydrolysis reaction coupled with bacterial destruction. Concentration of two different types of homoserine lactones (HSL) molecules was tested after the treatment at various rotational speeds. It was found that the strongest effects can be achieved at speeds > 2000 rpm. This value is considered as an onset speed of dominant cavitation, and it is in agreement with literature data. The experimental trends were in agreement with the calculations based on the finite element modelling, which show a significant increase in average shear stress at higher rotational speeds. Overall, the work has demonstrated the possible effects of hydrodynamic cavitation on the quorum-sensing molecules of Pseudomonas aeruginosa for the first time.

A new self-crosslinked composite hydrogel is prepared with chitosan (CS) and cationic guar gum (CGG), based on the imine and acetal chemistry for gelation. The CS/CGG hydrogel exhibits thermal/pH responsiveness, injectability, adhesiveness and good compressive strength. The hydrogel is effective in removing phosphate from wastewater through an adsorption process, during which KH 2 PO 4 is used as a phosphate model. The adsorption complies with the Freundlich model, indicating that it is a multilayered process with complex adsorption mechanisms. Considering their porous structure and nitrogen/phosphorus heteroatoms doping, the phosphate-adsorbed hydrogels are made into porous N,P doped carbon aerogels that can be potentially used as electrodes for a supercapacitor. The results indicate that these carbon aerogels possess excellent capacitive performance (best specific capacitance of 302.2 ± 4.9 F/g), as well as good cycling stability after 5000 times of charging/discharging., Competing Interests: Declaration of Competing Interest The authors declare no competing financial interest., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

In this work, silanized and aminated lignin (SAL) was synthesized in one step and its adsorption of Congo red and Cu(II) ions in aqueous solution was explored. Lignin was subjected to amine-silanization with (3-aminopropyl) triethoxysilane (APTES). Structural characterization substantiated successful amine-silanzation of lignin and formation of multi-layer APTES intermolecular crosslinked structure. The prepared SAL (nitrogen content = 6.1%) exhibited enhanced molecular weight, thermal stability, and water- and organic solvent-resistance properties. Additionally, the present of the porous structure of particle surface and an increase in the specific surface area and zeta potential promoted the accessibility of contaminants to the effective adsorption sites of SAL. Adsorption experiments showed that both Congo red and Cu(II) ion could be completely removed at original pH value, and their adsorption involved electrostatic attraction and complexation, respectively. The adsorption isotherms and kinetics were well described by the Langmuir and pseudo-second-order equations, respectively. The results showed that SAL is a promising adsorbent for the treatment of effluents., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Solar steam generation is one of the most promising technologies for desalination. In order to further promote the development of solar steam generation, a double-layer cellulose hydrogel (DCH) was designed and used as solar steam generation for seawater desalination. Under one sun illumination intensity (1 kW·m -2 ), the average evaporation rate and the steam evaporation efficiency reaches 1.582 kg·m -2  h -1 and 91.4 %, respectively. The durability test was performed to verify the long-time durability and antifouling property. Outdoor experiment was carried out to prove the high steam evaporation efficiency and desalination performance of DCH. This paves a way for the cellulose-based hydrogel as a biodegradable, low-cost and promising solar steam generation., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

In this study, the effect of ball milling on pyrite (FeS 2 ) promoting arsenic (As) removal by zero-valent iron (Fe 0 ) was investigated. The influences of different mass ratios of ball-milled FeS 2 /Fe 0 , the dosage of ball-milled FeS 2 /Fe 0 used and initial pH value were evaluated by batch experiments. The results showed that the ball-milled FeS 2 /Fe 0 system had a higher total As removal efficiency than the mixed FeS 2 -Fe 0 system, ball-milled FeS 2 and ball-milled Fe 0 systems in equal mass. Higher As removal efficiency in ball-milled FeS 2 /Fe 0 system was primarily related to the accelerated corrosion of Fe 0 , which was supported by the determination of total Fe 2+ release and electrochemical experiments. SEM-EDS and XPS characterizations revealed that there were iron sulfides (Fe(II)-S and Fe(III)-S) produced on the surface of Fe 0 in ball-milled FeS 2 /Fe 0 , which could facilitate the electron transfer of Fe 0 and enhanced the corrosion of it. BET test also indicated that ball-milled FeS 2 /Fe 0 possessed a higher specific surface area than ball-milled Fe 0 . In addition, the results also showed the optimum mass ratio of FeS 2 and Fe 0 in ball-milled FeS 2 /Fe 0 to remove As ([As(III)] = 2 mg/L) was 1:1, and the optimum dosage was 0.5 g/L, thereby indicating the optimal As:Fe 0 molar ratio was about 1:168. And the removal rate of As by ball-milled FeS 2 /Fe 0 was faster in acidic condition than that in alkaline condition. These findings suggest that Fe 0 -based arsenic removal efficiency can be enhanced by ball-milling with FeS 2 , making it more feasible for remediation of arsenic-polluted water., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

This study investigated the applicability of parallel factor analysis (PARAFAC) of fluorescence excitation-emission matrices (EEM) spectra to assess the formation potentials (FP) of carbonaceous and nitrogenous disinfection byproducts (C-DBP and N-DBP) and the FP reduction by the magnetic ion exchange resins, MIEX® DOC and MIEX® GOLD. Two source waters of different nature - a surface water and a secondary treated wastewater effluent - were studied. The samples were analyzed for formation potentials of trihalomethanes (THM 4 ), haloacetonitriles (HAN 4 ), haloketones (HK 2 ), and chloropicrin (CPN). A 4-component PARAFAC model was developed from 150 EEM samples generated from the raw source waters and their treatment with MIEX® resins. Components C1, C2, and C3 corresponded to humic-like dissolved organic matter (DOM) while C4 corresponded to protein-like DOM. Both MIEX® resins preferentially removed components C1, C2, and C3 over C4, indicating affinity with humic materials. MIEX® resins were shown to be more effective to treat surface water than secondary effluent, including effective removal of DBP precursors with extended bed volume treatment. Among all parameters investigated, THM 4 -FP strongly correlated with humic-like component C3, while HAN 4 -FP strongly correlated with protein-like component C4 (ρ > 0.89 and p < 0.01); CPN-FP and HK 2 -FP both correlated with anthropogenic DOM C2 (ρ > 0.89 and p < 0.01). Our results indicate that EEM-PARAFAC was valuable for assessing DBP formation potentials and removal of their precursors by MIEX® resins in different water sources., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

High efficiency lignin-grafted cationic polyacrylamide (L-CPA) flocculant was synthesized via "grafting to" method using acrylamide (AM), methylacryloyloxyethyltrimethyl ammonium chloride (DMC) and enzymatic hydrolysis lignin (EHL) as raw materials. The linear pre-polymer of cationic polyacrylamide (CPA) terminated with chlorine was first synthesized and then grafted onto EHL via reactions of chlorine with phenolic hydroxyl groups in lignin molecules. The synthesized L-CPA could self-assemble into octopus-like nanospheres with CPA segments dissolved in water and hydrophobic lignin skeletons concentrated in the core, which endowed the L-CPA with excellent flocculation efficiency for kaolin suspension under faintly acid, neutral or alkalescent conditions (pH = 5-9). Only a small dosage between 4.0-4.5 mg/L of L-CPA was needed for flocculation of the kaolin suspension. The charge neutralization and bridging effect was proposed for the flocculation mechanism of the lignin-grafted cationic polyacrylamide. The octopus-like L-CPA was cheap, environmentally friendly and technically feasible, showing a great prospect in wastewater treatment., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Anionic pectic substances in whitewater from papermaking are detrimental to machine operation and product quality. Pectinase was immobilized on pulp fiber using cationic polyacrylamide with layer-by-layer method to obtain bound enzyme with tunable activity and good performance for wastewater treatment. It was revealed that high charge density and low molecular weight for cationic polyacrylamide were advantageous for enzymatic activity. During the layer-by-layer adsorption process, the enzymatic activity of the immobilized enzyme increased nearly linearly with the layer number from 983 to 3074 U/g until the fourth layer. The stability of the four-layer immobilized enzyme was improved. The multilayer immobilized enzyme exhibited good reusability and storage stability compared with monolayer enzyme. At dosage of 10 U/mL, the cationic demand of the whitewater samples was reduced by 15% using four-layer immobilized enzyme. The results indicated a potential route to prepare immobilized enzyme with good performance for wastewater treatment in papermaking industry.

In this study, the enhanced effect of pyrite (FeS 2 ) on zero-valent iron (Fe 0 ) corrosion for arsenic (As) removal was investigated in a combined-Fe 0 /FeS 2 system. The effects of different Fe 0 /FeS 2 composition, dosage and initial pH were evaluated by batch experiments. Results showed that the best combination ratio of Fe 0 :FeS 2 (w/w) was 1:1 and the optimal dosage of mixture was 2.0 g/L. The combination of Fe 0 and FeS 2 in a system significantly enhanced the reactivity of Fe 0 for effective As removal within a broad pH range (3.0-9.0). The effective As removal in the combined-Fe 0 /FeS 2 system was primarily ascribed to being enhanced corrosion of Fe 0 by addition of FeS 2 . SEM and XRD characterizations strongly verified this point. Specifically, the mechanism study (the releases of Fe 2+ and total Fe ion, variations of pH values as well as XPS characterization) suggested that FeS 2 in the combined-Fe 0 /FeS 2 system could alleviate the passivation of Fe 0 (pH ini 3.0-5.0) and accelerate the dissolution of pristine oxide film that coated on Fe 0 surface (pH ini 6.8-9.0). Besides, FeS 2 in combined-Fe 0 /FeS 2 system could also accelerate the reactions between Fe 0 to O 2 at pH ini 3.0-9.0. These phenomena were well explained by a galvanic couple between Fe 0 and FeS 2 , where FeS 2 was a cathode and Fe 0 was an anode. Consequently, electrons released from Fe 0 that mediated by FeS 2 to oxide film, passivation layer and O 2 were accelerated in combined-Fe 0 /FeS 2 system and thereby enhanced the corrosion of Fe 0 for efficient As removal. Our findings suggest that utilizing FeS 2 to enhance the corrosion of Fe 0 would be a promising technology for remediation of As-contaminated water., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

We report an ingenious technique to prepare magnetic alkaline lignin-dopamine nanoparticles (AL-DA/Fe 3 O 4 NPs). Alkaline lignin, a kind of abundant waste from agriculture, pulping and bio-energy industry, was functionalized by the conjugation with DA molecules and nano-precipitation method. Benefiting from the three-dimensional network of lignin and mussel-inspired DA molecules, chromium(III) can be effectively removed by physisorption and chemisorption. The maximum Cr(III) adsorption capacity of AL-DA/Fe 3 O 4 NPs was found to be 44.56 mg/g, which was among the highest of previously reported biomass-based Cr(III) adsorbents. Moreover, sensitive magnetic responsiveness (24.6 emu/g) of AL-DA/Fe 3 O 4 NPs can be more helpful in recycling (over 90% recycled within 2 min) and multiple reusing. The preparation of this low-cost, high adsorptive capacity and good ecofriendly lignin-based nano-adsorbent is expected to become a sustainable technology to simultaneously achieve the wastewater reutilization from pulping and bio-energy industry and purification of other modern industries., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Nanotechnology has been identified as having great potential for improving the efficiency of water prevention and purification while reducing costs. In this field, two applications of nanocellulose have generated attention and have proven to be a sound strategy as an adsorbent and as a membrane for the removal of contaminants. This potential is attributed to its high aspect ratio, high specific surface area, high capacity retention, and environmental inertness. In addition to the aforementioned advantages, the presence of active sites allows the incorporation of chemical moieties that may enhance the binding efficiency of pollutants to the surface. This review paper intends to understand how nanocellulose affects the adsorption behavior of water pollutants, e.g., heavy metal ions, microbes, dyes, and organic molecules, and is divided in two parts. First, a general overview of the different strategies for the preparation of nanocellulose is described, and its specific properties are reported. The second section reports some of its application as adsorbent nanomaterial or separation membrane. It appears that the use of nanocellulose for these applications is very promising for wastewater treatment industries.

Advanced Oxidation Processes (AOPs) are the techniques employed for oxidation of various organic contaminants in polluted water with the objective of making it suitable for human consumption like household and drinking purpose. AOPs use potent chemical oxidants to bring down the contaminant level in the water. In addition to this function, these processes are also capable to kills microbes (as disinfectant) and remove odor as well as improve taste of the drinking water. The non-photochemical AOPs methods include generation of hydroxyl radical in absence of light either by ozonation or through Fenton reaction. The photochemical AOPs methods use UV light along with H 2 O 2 , O 3 and/or Fe +2 to generate reactive hydroxyl radical. Non-photochemical method is the commonly used whereas, photochemical method is used when conventional O 3 and H 2 O 2 cannot completely oxidize organic pollutants. However, the choice of AOPs methods is depended upon the type of contaminant to be removed. AOPs cause loss of biological activity of the pollutant present in drinking water without generation of any toxicity. Conventional ozonation and AOPs can inactivate estrogenic compounds, antiviral compounds, antibiotics, and herbicides. However, the study of different AOPs methods for the treatment of drinking water has shown that oxidation of parent compound can also lead to the generation of a degradation/transformation product having biological activity/chemical toxicity similar to or different from the parent compound. Furthermore, an increased toxicity can also occur in AOPs treated drinking water. This review discusses various methods of AOPs, their merits, its application in drinking water treatment, the related issue of the evolution of toxicity in AOPs treated drinking water, biocatalyst, and analytical methods for identification of pollutants /transformed products and provides future directions to address such an issue., (Copyright © 2018 Elsevier Inc. All rights reserved.)

In this study, a sequential Fe 0 /H 2 O 2 reaction and biological process was employed as a low-cost depth treatment method to remove recalcitrant compounds from coal-chemical engineering wastewater after regular biological treatment. First of all, a chemical oxygen demand (COD) and color removal efficiency of 66 and 63% was achieved at initial pH of 6.8, 25 mmol L -1 of H 2 O 2 , and 2 g L -1 of Fe 0 in the Fe 0 /H 2 O 2 reaction. According to the gas chromatography-mass spectrometer (GC-MS) and gas chromatography-flame ionization detector (GC-FID) analysis, the recalcitrant compounds were effectively decomposed into short-chain organic acids such as acetic, propionic, and butyric acids. Although these acids were resistant to the Fe 0 /H 2 O 2 reaction, they were effectively eliminated in the sequential air lift reactor (ALR) at a hydraulic retention time (HRT) of 2 h, resulting in a further decrease of COD and color from 120 to 51 mg L -1 and from 70 to 38 times, respectively. A low operational cost of 0.35 $ m -3 was achieved because pH adjustment and iron-containing sludge disposal could be avoided since a total COD and color removal efficiency of 85 and 79% could be achieved at an original pH of 6.8 by the above sequential process with a ferric ion concentration below 0.8 mg L -1 after the Fe 0 /H 2 O 2 reaction. It indicated that the above sequential process is a promising and cost-effective method for the depth treatment of coal-chemical engineering wastewaters to satisfy discharge requirements.

A novel superadsorbent anionic hydrogel was synthesized by grafting of poly (3-sulfopropyl methacrylate), P(SPMA), onto carboxymethyl cellulose (CMC). CMC-g-P(SPMA) superadsorbent hydrogel was applied as an efficient and sustainable adsorbent to remove methylene blue (MB) from waste water. Batch adsorption experiments showed that the solution pH had an obvious effect on the adsorption capacity with an optimal sorption pH at 6. The CMC-g-P(SPMA) hydrogel had rapid adsorption kinetics for MB and the adsorption equilibrium reached within 40min. The adsorption kinetics were more accurately described by pseudo second-order model and the Langmuir-fitted adsorption isotherms revealed a maximum capacity of 1675mg/g. The current anionic hydrogel is reusable as the adsorption capacity remained at 89% level after five adsorption-desorption cycles. CMC-g-P(SPMA) hydrogel was presented as a sustainable promising adsorbent with high adsorption capacity and good regenerability for effective cationic dyes removal., (Copyright © 2017 Elsevier B.V. All rights reserved.)

Bacterial cellulose (BC) is a green biopolymer suitable for heavy metal ion removal from aqueous solution due to its nano-porous microstructure. Polyethyleneimine-bacterial cellulose (PEI-BC) was prepared by reductive amination of dialdehyde BC with polyethyleneimine. The capacity of PEI-BC in Cu(II) and Pb(II) adsorption from aqueous solution was investigated. The adsorption kinetics could be well expressed by pseudo-second-order model and the adsorption isotherm data were well fitted with Freundlich model. Adsorption processes of Cu(II) and Pb(II) by PEI-BC reached equilibrium very rapid in 30 and 60min, respectively. The maximum adsorption capacity of PEI-BC on Cu(II) and Pb(II) was found to be 148 and 141mg/g, respectively, which was higher than that of unmodified BC and other modified BC reported. PEI-BC also showed good reusability in the adsorption of Cu(II) and Pb(II). This study demonstrates that polyethyleneimine modification makes BC a potential bioadsorbent for heavy metal ion removal in waste water., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

A water-compatible magnetic triclosan (TCS) imprinted material (TCS-CTS-Fe 0 -MIPs) was synthesized for selective enrichment and detection of TCS in real complex water samples. The material was synthesized by using chitosan (CTS) as functional monomer, which has rich surface O- and N-containing functional groups. The TCS imprinted CTS was coated on Fe 0 surface and then cross-linked with glutaraldehyde. Scanning electron microscopy suggested that the imprinted material was covered with a layer of imprinted film, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy confirmed that the imprinted material had more functional groups (amino and hydroxyl groups) than that of non-imprinted material. The TCS imprinted and non-imprinted materials used in each adsorption experiments were 0.1 mg mL -1 . The maximum adsorption capacity of the TCS imprinted material and non-TCS imprinted material were 20.86 and 15.11 mg g -1 , respectively. The adsorption results showed that selectivity coefficient was 10.151, 1.353, and 8.271 in the presence of p-chlorophenol, 2,4,6-trichlorophenol, and bisphenol-A, respectively. The recoveries of river water and lake water samples were 92.8, 91.3, 92.4, and 81.4, 82.3, 82.1%, respectively, when the samples were spiked with 4, 6, and 8 μg L -1 of TCS with the imprinted material. The adsorption capacity of the TCS imprinted material and non-TCS imprinted material lost 5.2 and 6.2% after six times of recycling. The high selectivity and excellent adsorption capacity of the imprinted material can be attributed to the presence of sterically complementary imprinted sites and high surface, which would also made it more accessible to TCS than that of non-imprinted material. The present study would provide an environmental friendly and convenient method for the removal and the monitoring of TCS in environmental water samples.

A one-pot bio-iron system was established to investigate synergetic abiotic and biotic effects between iron and microorganisms on Cr(VI) removal. More diverse iron corrosion and reactive solids, such as green rusts, lepidocrocite and magnetite were found in the bio-iron system than in the Fe 0 -H 2 O system, leading to 4.3 times higher Cr(VI) removal efficiency in the bio-iron system than in the Fe 0 -H 2 O system. The cycling experiment also showed that the Cr(VI) removal capacity of Fe 0 in the bio-iron system was 12.4 times higher than that in the Fe 0 -H 2 O system. A 62days of life-span could be achieved in the bio-iron system, while the Fe 0 -H 2 O system lost its efficacy after 30days. Enhanced effects of extra Fe 2+ on Cr(VI) removal was observed, largely contributed to the adsorbed Fe 2+ on iron surface, which could function as an extra reductant for Cr(VI) and promote the electron transfer on the solid phase. The results also showed that the reduction of Cr(VI) by microorganisms was insignificant, indicating the adsorption/co-precipitation of Cr by iron oxides on iron surface was responsible for the overall Cr(VI) removal. Our study demonstrated that the bio-amended iron corrosion could improve the performance of Fe 0 for Cr(VI) removal from groundwater., (Copyright © 2017 Elsevier B.V. All rights reserved.)

Water-resistant cellulose foam paper was developed in this work in an attempt to improve the antimicrobial activity of cellulose foam paper for capture and deactivation of pathogenic microorganisms existed in water. Results indicated that the cellulose foam paper could significantly improve household water quality by incorporating guanidine-based polymer modified with starch or called antibacterial thermoplastic starch (ATPS) into fibre network in the presence of proper amount of fiber fines. Ring diffusion testing demonstrated that no ATPS diffused around or underneath of samples, verifying that cellulose foam filter added by ATPS were of non-leaching type. Furthermore, the viability of bacteria before and after filtering and the structure of cellulose foam paper were analyzed via fluorescence microscopy and scanning electron microscopy images. The findings further proved the effectiveness of antimicrobial cellulose foam in deactivating pathogens, E.coli in particular., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

In order to expand the potential applications of metal-organic frameworks (MOFs), structure directing agents modified mesoporous MIL-53(Al) (MIL-53(Al)-1) was investigated to adsorb triclosan (TCS) with two different initial concentrations. MIL-53(Al)-1 with high mesoporosity and total pore volume exhibited higher adsorption capacity and 4.4 times faster adsorption of TCS at low concentration (1 mg L -1 ) than that of microporous MIL-53(Al). Also, mesoporous as well as microporous MIL-53(Al) showed significant higher adsorption capacity and two orders of magnitude greater fast uptake of TCS than two kinds of mesoporous-activated carbon. The adsorption of TCS onto MIL-53(Al)-1 released more energy and had higher disorderliness than TCS on MIL-53(Al). The superior adsorption characteristics of MIL-53(Al)-1 were preserved over a wide pH range (4-9), at high concentration of ionic strengths, and in the presence of coexisting compounds (anions, cations, phenol, aniline, and humic acid). The selectivity adsorption and Fourier transform infrared (FT-IR) spectra revealed that TCS adsorption on MIL-53(Al)s was mainly driven by hydrophobicity interaction assisted with hydrogen bonding on MIL-53(Al)s. MIL-53(Al)s can be effectively regenerated several times by washing with 90% methanol-water (pH 11). All of the above results demonstrated MIL-53(Al)s are promising adsorbents for water purification. Graphical abstract.

Herein a Mn-deposited sepiolite catalyst was obtained through a facile co-precipitation method, and then used as the heterogeneous ozonation catalysts applied to the tertiary treatment of regenerated-papermaking wastewater. During the process, the as-prepared catalyst was endowed with higher Brunauer-Emmett-Teller specific surface area of 412.3 m 2 /g compared to 124.6 m 2 /g of the natural sepiolite. Hence, in the adsorption of methylene blue, the as-prepared catalyst was observed with a very high removal rate of 96.2% although a little lower than the modified sepiolite of 97.5% in 100 min. And for practical application, the catalyst was used for treating the effluent from regenerated-papermaking industry, via a heterogeneous catalytic ozonation process. Consequently, the highest color removal rate of 99.5%, and the highest chemical oxygen demand (COD) removal efficiency of 73.4% were achieved in 20 and 30 min, respectively. As a result, the treated wastewater was more biodegradable and less toxic; the biochemical oxygen demand (BOD 5 )/COD value could reach 0.41. Moreover, the catalyst showed superior stability at successive ozonation runs. The main possible reaction pathway is also presented. The results indicate that catalytic ozonation was proved to be effective when Mn/sepiolite was used as catalysts applied to the advanced treatment of regenerated-papermaking wastewater.

The unique electrocoagulator proposed in this study is highly efficient at removing Ni-EDTA, providing a potential remediation option for wastewater containing lower concentrations of Ni-EDTA (Ni ≤ 10 mg L -1 ). In the electrocoagulation (EC) system, cylindrical graphite was used as a cathode, and a packed-bed formed from iron scraps was used as an anode. The results showed that the removal of Ni-EDTA increased with the application of current and favoured acidic conditions. We also found that the iron scrap packed-bed anode was superior in its treatment ability and specific energy consumption (SECS) compared with the iron rod anode. In addition, the packed density and temperature had a large influence on the energy consumption (ECS). Over 94.3% of Ni and 95.8% of TOC were removed when conducting the EC treatment at an applied current of 0.5 A, initial pH of 3, air-purged rate 0.2 L min -1 , anode packed density of 400 kg m -3 temperature of 313 K and time of 30 min. SEM analysis of the iron scraps indicated that the specific area of the anode increased after the EC. The XRD analysis of flocs produced during EC revealed that hematite (α-Fe 2 O 3 ) and magnetite (Fe 3 O 4 ) were the main by-products under aerobic and anoxic conditions, respectively. A kinetic study demonstrated that the removal of Ni-EDTA followed a first-order model with the current parameters. Moreover, the removal efficiency of real wastewater was essentially consistent with that of synthetic wastewater., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Zeolite was synthesized from coal fly ash by a fusion method and was used for the removal of heavy metal ions (Pb(2+), Cd(2+), Cu(2+), Ni(2+), and Mn(2+)) in aqueous solutions. Batch method was employed to study the influential parameters such as adsorbent dosage, pH, and coexisting cations. Adsorption isotherms and kinetics studies were carried out in single-heavy and multiheavy metal systems, respectively. The Langmuir isotherm model fitted to the equilibrium data better than the Freundlich model did, and the kinetics of the adsorption were well described by the pseudo-second-order model, except for Cd(2+) and Ni(2+) ions which were fitted for the pseudo-first-order model in the multiheavy metal system. The maximum adsorption capacity and the distribution coefficients exhibited the same sequence for Pb(2+) > Cu(2+) > Cd(2+) > Ni(2+) > Mn(2+) in both single- and multiheavy metal systems. In the end, the adsorption capacity of zeolite was tested using industrial wastewaters and the results demonstrated that zeolite could be used as an alternative adsorbent for the removal of heavy metal ions from industrial wastewater.

Synthetic filters are neither biodegradable nor produced from renewable sources. Thus, their disposal has serious environmental impacts. There is a growing desire to produce filters from cellulosic fibers that are renewable, biodegradable, cheap and most importantly recyclable if the contamination is removed. Foam-laid process in papermaking is a promising process for the production of specialty papers. Filters produced using this process are capable of providing products with high specific surface area and tortuous structure favorable for entrapping particulate matters, while providing excellent permeability for incoming gas or liquid. Although the end product fulfills completely the requirement of a filter in a dry environment, it fails completely if it is exposed to a moist environment. This work reports on converting the hydrophilic cellulosic filter into a hydrophobic product without disturbing its original structure.

A novel nanocomposite microgel based on nanocellulose and amphoteric polyvinylamine (PVAm) was fabricated via a two-step method. Firstly, cellulose nanocrystal was oxidized by sodium periodate to yield dialdehyde nanocellulose (DANC). DANC was then used as a crosslinker to react with PVAm to obtain a pH responsive microgel with high density of free amine groups. The microgel was characterized using FTIR, XRD, AFM and elemental analysis. AFM images revealed that the nanocomposite was microspherical particles with a diameter ranging from 200 to 300nm. The microgel was found to be effective in anionic dye removal at acidic conditions. The adsorption isotherms for congo red 4BS, acid red GR and reactive light yellow K-4G fit well with the Sips model, and the maximum adsorption capacities were 869.1mgg(-1), 1469.7mgg(-1) and 1250.9mgg(-1), respectively. The adsorption for these three anionic dyes all followed pseudo second order kinetics, indicating a chemisorption nature., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

This study aimed to produce furfural from waste aqueous hemicellulose solution of a hardwood kraft-based dissolving pulp production processing in a green method. The maximum furfural yield of 82.4% and the xylose conversion of 96.8% were achieved at 463K, 1.0g ZSM-5, 1.05g NaCl and organic solvent-to-aqueous phase ratio of 30:15 (V/V) for 3h. The furfural yield was just 51.5% when the same concentration of pure xylose solution was used. Under the optimized condition, furfural yield was still up to 67.1% even after the fifth reused of catalyst. Catalyst recycling study showed that ZSM-5 has a certain stability and can be efficiently reused., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Iron reduction and sulfate reduction often occur simultaneously in anoxic systems, and where that is the case, the molar ratio between the reactions (i.e., Fe/SO42− reduced) influences their impact on water quality and carbon storage. Previous research has shown that pH and the supply of electron donors and acceptors affect that ratio, but it is unclear how their influences compare and affect one another. This study examines impacts of pH and the supply of acetate, sulfate, and goethite on the ratio of iron to sulfate reduction in semi‐continuous sediment bioreactors. We examined which parameter had the greatest impact on that ratio and whether the parameter influences depended on the state of each other. Results show that pH had a greater influence than acetate supply on the ratio of iron to sulfate reduction, and that the impact of acetate supply on the ratio depended on pH. In acidic reactors (pH 6.0 media), the ratio of iron to sulfate reduction decreased from 3:1 to 2:1 as acetate supply increased (0–1 mM). In alkaline reactors (pH 7.5 media), iron and sulfate were reduced in equal proportions, regardless of acetate supply. Secondly, a comparison of experiments with and without sulfate shows that the extent of iron reduction was greater if sulfate reduction was occurring and that the effect was larger in alkaline reactors than acidic reactors. Thus, the influence of sulfate supply on iron reduction extent also depended on pH and suggests that iron reduction grows more dependent on sulfate reduction as pH increases. Our results compare well to trends in groundwater geochemistry and provide further evidence that pH is a major control on iron and sulfate reduction in systems with crystalline (oxyhydr)oxides. pH not only affects the ratio between the reactions but also the influences of other parameters on that ratio. [ABSTRACT FROM AUTHOR]