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In this study, three sequencing batch biofilter granular reactors (SBBGRs) were employed to treat model lignin wastewater containing different lignin models (2,6-dimethoxyphenol, 4-methoxyphenol, and vanillin). After 40 days of cultivation, uniform-shaped aerobic granular sludge (AGS) was successfully developed through nutrient supplementation with synthetic wastewater. During the acclimation stage, the chemical oxygen demand (COD) reduction efficiencies of the three reactors showed a trend of initial decreasing (5-20%) and then recovering to a high reduction efficiency (exceeding 90%) in a short period of time. During the stable operation stage, all three reactors achieved COD reduction efficiencies exceeding 90%. These findings indicated the cultivated AGS's robust resistance to changes in lignin models in water. UV-Vis spectra analysis confirmed the effective degradation of the three lignin models. Microbiological analysis showed that Proteobacteria and Bacteroidetes were always the dominant phyla. At the genus level, while Acinetobacter (15.46%) dominated in the inoculation sludge, Kapabacteriales (7.93%), SBR1031 (11.77%), and Chlorobium (25.37%) were dominant in the three reactors (for 2,6-dimethoxyphenol, 4-methoxyphenol, and vanillin) after degradation, respectively. These findings demonstrate that AGS cultured with SBBGR effectively degrades lignin models, with different dominant strains observed for various lignin models., Competing Interests: The authors declare there is no conflict., (© 2024 The Authors This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC BY 4.0), which permits copying, adaptation and redistribution, provided the original work is properly cited (http://creativecommons.org/licenses/by/4.0/).)

Advanced oxidation technologies based on hydroxyl radical (•OH) and sulfate radical (SO 4 -• ) are two common types of advanced oxidation technologies, but there are not many reports on the application of advanced oxidation methods in actual wastewater pretreatment. This article compares the pre-treatment performance of Fe 2+ /H 2 O 2 and Fe 2+ /Persulfate systems in actual pharmaceutical wastewater, and combines EEM, GC-MS, and toxicity testing results to explore the differences in TOC, COD, and NH 3 -N removal rates, optimal catalyst dosage, applicable pH range, toxicity of effluent after reaction, and pollutant structure between the two systems. The results indicate that the Fe 2+ /H 2 O 2 system has a higher pollutant removal rate (TOC: 71.9%, COD: 66.9%, NH 3 -N: 34.1%), but also requires a higher catalyst (Fe 2+ ) concentration (6.0 g/L), and its effluent exhibits characteristic peaks of aromatic proteins. The Fe 2+ /Persulfate system has a wider pH range (pH ≈ 3-7) and is more advantageous in treating wastewater containing more cyclic organic compounds, but the effluent contains some sulfur-containing compounds. In addition, toxicity tests have shown that the toxicity reduction effect of the Fe 2+ /Persulfate system is stronger than that of the Fe 2+ /H 2 O 2 system.

Microcystins with leucine arginine (MC-LR) is a virulent hepatotoxin, which is commonly present in polluted water with its demethylated derivatives [Dha 7 ] MC-LR. This study reported a low-cost molecularly imprinted polymer network-based electrochemical sensor for detecting MC-LR. The sensor was based on a three-dimensional conductive network composed of multi-walled carbon nanotubes (MWCNTs), graphene quantum dots (GQDs), and gold nanoparticles (AuNPs). The molecularly imprinted polymer was engineered by quantum chemical computation utilizing p-aminothiophenol (p-ATP) and methacrylic acid (MAA) as dual functional monomers and L-arginine as a segment template. The electrochemical reaction mechanism of MC-LR on the sensor was studied for the first time, which is an irreversible electrochemical oxidation reaction involving an electron and two protons, and is controlled by a mixed adsorption-diffusion mechanism. The sensor exhibited a great detection response to MC-LR in the linear range of 0.08-2 μg/L, and the limit of detection (LOD) is 0.0027 μg/L (S/N = 3). In addition, the recoveries of the total amount of MC-LR and [Dha 7 ] MC-LR in the actual sample by the obtained sensor were in the range from 91.4 to 116.7%, which indicated its great potential for environmental detection.

Sewage treatment plants (STPs) are significant routes through which microplastics (MPs) are released into the aquatic environment. Constructed wetland is an effective facility for deep treatment of tailwater. At present, research on the removal of MPs in the tailwater of STPs by multi-stage constructed wetlands is limited. This work investigated and analyzed the removal characteristics of MPs in the tailwater treatment system of Cihu wetland park in Huangshi, Hubei Province of China. The abundance/removal of MPs in the Cihu Lake-wetland microcosm system was investigated. The results showed that the multi-stage constructed wetlands achieved a total removal rate of 94.7% for MPs with 2.2 particles/L MPs in the effluent. The removal rates of MPs reached 89 and 37.5%, respectively, in the (horizontal/vertical) subsurface flow constructed wetland and surface flow constructed wetland. The abundance of MPs in receiving water of Cihu Lake substantially decreased due to the dilution of wetland effluents. This study partially bridged the knowledge gap hypothesis on the treatment of MPs in tailwater by multi-stage constructed wetlands.

Excessive phosphorus causes eutrophication problems. The adsorptive removal of phosphate is prevalent and practical in large-scale applications, such as column adsorption. A metal organic framework (MOF)-enhanced layered double hydroxide (LDH) adsorbent material was developed and studied for batch adsorption and then combined with polyacrylonitrile (PAN) to form MOF/LDH/PAN composite beads working as a functional material for columns. Scanning electron microscopy (SEM) images showed the well-dispersed adsorbent powder in porous composite beads. The Fowler-Guggenheim isotherm model described the phosphate adsorption behavior of the MOF/LDH powder with a maximum capacity of 74.96 mg P/g. Mass transfer in the composite beads was successfully described with the Fickian diffusion model. The composite-packed fixed bed treated 37.95 BVs of the influent (55.51 mg P/L phosphate solution) and achieved an uptake of 18.92 mg P/g, with a removal efficiency of 96.42%, before the breakthrough point in the column study. The phosphate-loaded composite bed was regenerated with 0.1 M NaOH to 70% efficiency within 30 BVs. The polymer composite can be considered a practical solution for adsorption-based water treatment applications in tank and column processes where powder adsorbents cannot be applied.

In this study, the effect of arsenic on the sulfamethoxazole (SMX) removal efficiency and microbial community structure was investigated over 60 days using the SBR process. The results showed that the presence of arsenic had no significant impact on the system performance, the removal efficiencies of two reactors, R1 (the control test) and R2 (with the addition of arsenic), were 13.36 ± 5.71 and 14.20 ± 5.27%, which were attributed to the adsorption of SMX by fulvic acid-like substances and tryptophan-like proteins of extracellular polymeric substances. Compared to the seed sludge, the species number indicated that R2 possessed the richer diversity, while R1 possessed the lower diversity on day 60, which might be relative to the transferring of antibiotic resistance genes (ARGs) in sludge bacterial communities; the minute amounts of arsenic could make the relative levels of Sul1 and Sul2 genes which encode ARGs of sulfonamides in R2 (2.07 and 2.47%) be higher than that in R1 (1.65 and 1.27%), which made the bacterial community of the R2 system more adaptable to SMX stress. Therefore, the minute amounts of arsenic weakened the effect of SMX on the system and enhanced the stability of the microbial community structure.

The detoxification of dye-contaminated water by photocatalysis has become a research priority. Here, a novel hybrid material, cuprous oxide/sunflower stem pith (Cu 2 O/SSP), was successfully synthesized in situ, using copper hydroxide gel, prepared by ion exchange, as the precursor to Cu 2 O. The presence of Cu 2 O nanoparticles on the SSP was confirmed by scanning electron microscopy, Fourier transform infrared spectroscopy and X-ray diffraction analyses. Using methylene blue (MB) as the target pollutant, Cu 2 O/SSP delivered excellent adsorption-photocatalytic degradation and was readily photoregenerated. Cu 2 O/SSP removed 72.7% of MB after 60 min under visible light irradiation, an increase of 15.6 % compared with unmodified SSP. SSP plays three roles in the removal of MB: it acts as an adsorbent for the MB, a carrier for the Cu 2 O nanoparticles and it also inhibits photocorrosion of Cu 2 O. The mechanism of adsorption-photocatalysis by Cu 2 O/SSP was investigated and a description of the mechanism is provided. This study paves the way for the detoxification of dye-containing wastewater using hybrid biomass materials.

Pulp and paper wastewater (PPWW) contains numerous refractory and harmful contaminants that require advanced treatment to meet the discharge criteria. This study compared the efficacy of two PPWW treatments: ultraviolet/peroxymonosulfate (UV/PMS) and ultraviolet/H 2 O 2 (UV/H 2 O 2 ) working under similar circumstances. The initial pH value, oxidant dosage, UV radiation intensity, and pseudo-first-order constant k obs were systematically studied in both systems. Optimally, the UV/PMS process produced an effluent of higher quality than the UV/H 2 O 2 , as measured by the removal efficiencies of chemical oxygen demand (COD) in 60 min, which were 48.2 and 64.3% for the respective UV/H 2 O 2 and UV/PMS processes and corresponding k obs values of 0.0102 and 0.0159 min -1 , respectively. Radical scavenging experiments demonstrated that •OH was the primary reactive oxygen species in UV/H 2 O 2 process, and •OH and SO 4 • in the UV/PMS process. Moreover, ultraviolet-visible spectroscopy and gas chromatography coupled mass spectroscopy analyses showed that deep treatment of petroleum hydrocarbons with carbon chain lengths greater than 18 and macromolecular semi-volatile organic compounds in paper wastewater is difficult, whereas the UV/PMS process can significantly improve the removal of amides, esters, phenols, and other aromatic compounds.- • in the UV/PMS process. Moreover, ultraviolet-visible spectroscopy and gas chromatography coupled mass spectroscopy analyses showed that deep treatment of petroleum hydrocarbons with carbon chain lengths greater than 18 and macromolecular semi-volatile organic compounds in paper wastewater is difficult, whereas the UV/PMS process can significantly improve the removal of amides, esters, phenols, and other aromatic compounds.

Synthetic organic pollutants emanating continuously in the ecosystem have become a global concern because of their toxicity and persistent nature. Bisphenol A (BPA) is one such pollutant which threatens public health and safety. It is a monomer used in manufacturing plastics, polycarbonate resins, epoxy resins and is a well-recognised endocrine disruptor mimicking estrogen. BPA leaches into food and beverages stored in containers causing contamination issues. Its widespread exposure and potential toxicity is an environmental health concern. In this review, a systematic investigation has been carried out on the heterogeneous catalysts used for Fenton-like processes for BPA degradation. The Fenton-like reaction is one such reaction that is used for wastewater remediation purposes. The reaction advances through the generation of powerful oxidizing radicals like •OH and SO 4 •- in the presence of a suitable catalyst. The application of various Fenton catalysts, with their distinguished morphological characteristics, oxidizing properties, toxicity analysis, and the present state of the art of BPA degradation by these catalysts, have been documented in the current work. This review also highlights a few challenges and prospects for analysing degradation products of landfill leachate.

In this study, we investigated using the main composition of pipe deposits from water distribution networks as catalyst to activate dual-oxidant H 2 O 2 /Na 2 S 2 O 8 system to produce radicals for perchloroethylene and chloramphenicol removal. According to the results, the degradation efficiency of perchloroethylene by H 2 O 2 /Na 2 S 2 O 8 system was 92.05% within 8 h. Due to the slow conversion between ≡Fe 3+ and ≡Fe 2+ , the hydroxylamine was introduced to reduce reaction time. As for the results, the degradation efficiency of chloramphenicol in the H 2 O 2 /Na 2 S 2 O 8 system with hydroxylamine assistance was 73.31% within 100 min. Meanwhile, several key affecting factors and the kinetic models were investigated. The primary radicals were identified by electron paramagnetic resonance and radical scavenging tests. Eleven degradation products were confirmed by high-resolution liquid chromatography-mass spectrometry. The result of this study provided the theoretical basis for resource utilization of pipe deposits in water treatment in case of emerging contamination events.

The effects of pure oxygen aeration on compositional characteristics of soluble microbial products (SMP) and extracellular polymeric substances (EPS) of the activated sludge acclimated in a sequential batch reactor (SBR) were explored in batch mode. The structure of the extracellular products would change with different aeration methods or aeration rates. The proportion of SMP of most oxygen aerated sludge was less than 10%, while that in air aerated sludge was as high as 30-40%. The proportion of TB-EPS decreased from 56.95% to 30.63%, and the proportion of LB-EPS increased obviously with the increase of oxygen aeration rate. The contents of the protein (PN) and the polysaccharide (PS) of extracellular products with oxygen aeration were significantly different, and the PN was much higher than PS (p < 0.05). The zeta potential of each component in activated sludge was negative, gradually decreasing with the progress of biological treatment. The fluorescence peaks in SMP, LB-EPS and TB-EPS with pure oxygen aeration were attributed to tryptophan PN-like and humic acid-like fractions. The results showed that the proportion of the components in the extracellular products could be regulated by adjusting the aeration rate and aeration mode, so as to optimize the treatment process of activated sludge.

Surface water contamination has emerged as an area of major concern in rapidly growing cities in the Global South, including and especially in the Indian megacity context. We argue here that nallahs (open drainage channels in Indian megacities) should be more widely recognized as a potential locus of intervention. These combined stormwater and wastewater networks offer opportunities for flexible, frugal and inclusive retrofits to improve surface and groundwater quality. We propose and define the concept of provisional green infrastructure (PGI) as a speculative innovation typology describing in-stream interventions. We argue that PGI should be employed as a shared boundary concept guiding transdisciplinary action and research within the highly unpredictable, space-constrained, and contaminated watersheds. Citing case studies throughout the region and ongoing research in the city of Bangalore, we demonstrate in-stream modifications may be capable of achieving significant improvement in the quality of urban wastewater and may play a complementary role in closing persistent capacity gaps in the operation of both centralized and decentralized treatment practices within megacities. Anticipating the larger diffusion of PGI practices across the region by various early adopters and non-state actors, we suggest a cogent research agenda focused on identifying various generalizable 'upscaling' opportunities for deploying in-stream interventions across various organizational and spatial domains.

This study focused on using pH as a single indicator to evaluate/control the performance of the nitritation system under the influence of three major operational parameters, and a total of fifteen batch tests were conducted. Results indicated that there were important interactions among different operational parameters and pH in the nitritation system; it was possible to propose the optimal nitritation operation scheme to compensate for negative changes in operational parameters. The optimal carbon to nitrogen (C/N) ratio was kept at 2.0 to ensure efficient removal of ammonium. The reaction time was the lowest (150 min) with the temperature = 20 °C, C/N = 0, and sludge/water ratio = 1:1. However, the C/N ratio could be adjusted to close to zero by reducing the temperature to about 10 °C, weakening the heterotrophic bacteria, and supplying sufficient biomass. The C/N ratio and sludge/water ratio could also be set at 4.0 and 1:3 respectively to deal with the impact of low temperature and organic matter. Results of this study might be useful to explain the optimal conditions and process control schemes with pH as a single indicator.

Optimal operation of membrane bioreactor (MBR) plants is crucial to save operational costs while satisfying legal effluent discharge requirements. The aeration process of MBR plants tends to use excessive energy for supplying air to micro-organisms. In the present study, a novel optimal aeration system is proposed for dynamic and robust optimization. Accordingly, a deep reinforcement learning (DRL)-based optimal operating system is proposed, so as to meet stringent discharge qualities while maximizing the system's energy efficiency. Additionally, it is compared with the manual system and conventional reinforcement learning (RL)-based systems. A deep Q-network (DQN) algorithm automatically learns how to operate the plant efficiently by finding an optimal trajectory to reduce the aeration energy without degrading the treated water quality. A full-scale MBR plant with the DQN-based autonomous aeration system can decrease the MBR's aeration energy consumption by 34% compared to other aeration systems while maintaining the treatment efficiency within effluent discharge limits.

In this study, the completely autotrophic nitrogen removal over nitrite (CANON) process was initiated in a sequencing batch biofilm reactor (SBBR). Then the reactor was operated under different IC/N ratios. The total inorganic nitrogen removal efficiency (TINRE) at IC/N ratios of 0.75, 1.0, 1.25, 1.5 and 2.0 were 37.0 ± 11.0%, 58.9 ± 10.2%, 73.9 ± 3.2%, 73.6 ± 1.8% and 72.6 ± 2.0%, respectively. The suitable range of IC/N ratio in this research is 1.25-2.0. The poor nitrogen removal performance at IC/N ratio of 0.75 was due to the lack of growth substrate for AnAOB and low pH simultaneously; at IC/N ratio of 1.0 this was because the substrate concentration was insufficient for fully recovering the AnAOB activities. Microbial analysis indicated that Nitrosomonas, Nitrospira and Candidatus Brocadia were the main ammonium oxidation bacteria (AOB), nitrite oxidation bacteria (NOB) and anammox bacteria (AnAOB), respectively. In addition, at IC ratios of 1.25 or higher, denitrification was promoted with the rise of IC/N ratio, which might be because the change of IC concentrations caused cell lysis of microorganisms and provided organic matter for denitrification.

A fiber-network chitosan film with three-dimensional interconnected structure was prepared in an alkali/urea solution and regenerated from an ethanol/water coagulation solution. The surface morphology and structure were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), N 2 adsorption-desorption, attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) and X-ray photoelectron spectroscopy (XPS). Batch adsorption for uranium U(VI) was conducted to investigate the effects of pH, contact time and initial uranium concentration on adsorption capacity. The adsorption of CS-80% was in good agreement with the pseudo-second-order kinetic model and Langmuir isotherm model. The three-dimensional interconnected structure provided more active sites and favored the diffusion of uranium solute, and therefore enhanced the adsorption capacity. The maximum adsorption capacity at pH 5 was 196.735 mg/g. The adsorption mechanism was attributed to chelation and coordination of uranium with -NH 2 and -OH groups on chitosan molecules.

Adsorption behaviors of methylene blue (MB) from aqueous solution using sunflower stem pith (SSP) as adsorbent were investigated. The effects of adsorption conditions such as adsorption time, initial concentration of MB and dosage of SSP on the detoxification of MB were examined. The equilibrium adsorption data were analyzed using three well-known isotherms: Langmuir, Freundlich and Temkin. The results indicated that the Langmuir isotherm fitted well to the data as compared with another isotherm model. The maximum adsorption capacity calculated by the Langmuir isotherm model was 277 mg/g at 338 K. Kinetic analyses were conducted using pseudo first order, pseudo second order and the Elovich model. The regression results showed that the MB adsorption was described by the pseudo second order model. Different thermodynamic parameters such as Gibb's free energy (ΔG o ), standard enthalpy change (ΔH o ) and standard entropy change (ΔS o ) were also evaluated. The results showed that the detoxification of MB using SSP as adsorbent was feasible, non-spontaneous and exothermic under experimental conditions.

This study investigated the performance of coagulation with ferric chloride (FeCl 3 .6H 2 O) and adsorption with activated carbon used as pretreatments prior to thin-film composite-forward osmosis (TFC-FO) filtration of ink printing wastewater. Wastewater samples were collected from a printing factory located in Chao Phraya river basin where zero liquid-discharge standards are regulated. The FO filtration unit was operated in co-current mode with the cross-flow velocity of 600 mL/min using 2 M NaCl as draw solution. The FO membrane achieved 83.9-91.0% chemical oxygen demand and 91.2-99.9% color rejections. FO filtration of raw wastewater, coagulation-treated wastewater, and coagulation and adsorption-treated wastewater resulted in 56.3%, 49.0% and 46.1% of flux decline in 150 min. Scanning electron microscopy and Fourier transform infrared spectrometry results revealed that cake formation caused by colloidal particles and pore blocking from precipitation were the major fouling mechanisms. Cake-enhanced concentration polarization also promoted adsorption of color and pigments at the membrane surface. Both fouling mechanisms were successfully mitigated by adsorption following coagulation pretreatment. Overall, the combined pretreatments and FO have potential for the effective treatment and reuse of ink printing wastewater.

The wastewater industry is currently facing dramatic changes, shifting away from energy-intensive wastewater treatment towards low-energy, sustainable technologies capable of achieving energy positive operation and resource recovery. The latter will shift the focus of the wastewater industry to how one could manage and extract resources from the wastewater, as opposed to the conventional paradigm of treatment. Debatable questions arise: can the more complex models be calibrated, or will additional unknowns be introduced? After almost 30 years using well-known International Water Association (IWA) models, should the community move to other components, processes, or model structures like 'black box' models, computational fluid dynamics techniques, etc.? Can new data sources - e.g. on-line sensor data, chemical and molecular analyses, new analytical techniques, off-gas analysis - keep up with the increasing process complexity? Are different methods for data management, data reconciliation, and fault detection mature enough for coping with such a large amount of information? Are the available calibration techniques able to cope with such complex models? This paper describes the thoughts and opinions collected during the closing session of the 6th IWA/WEF Water Resource Recovery Modelling Seminar 2018. It presents a concerted and collective effort by individuals from many different sectors of the wastewater industry to offer past and present insights, as well as an outlook into the future of wastewater modelling.

A liquid-gas two-phase computational fluid dynamics (CFD) model was developed to simulate flow field and gas hold-up in a pilot-scale oxidation ditch (OD). The volume of fluid (VOF) model and the mass flow inlet boundary condition for gas injection were introduced in this model. The simulated values of the flow velocities and the gas hold-up were verified by experimental measurements in the pilot-scale OD. The results showed that the gas hold-up at test-site 3, immediately downstream of the surface aerator, was the highest among all three test-sites. Most of the gas existed in the upper portion of the ditch and was close to the inner side of the channel. Based on the liquid-gas two-phase CFD model, three operating conditions with different setting height ratios of the submerged impellers were simulated. The simulated results suggested that the setting heights of the submerged impellers have significant impacts on the flow velocity distribution. Lowering the setting height could increase the flow velocity in the pilot-scale OD. An optimal setting height ratio of 0.273 was proposed, which would be beneficial for minimizing sludge sedimentation, especially near the inner side of the curve bend.

Chemical oxygen demand (COD), an important indicative measure of the amount of oxidizable pollutants in wastewater, is often analyzed off-line due to the expensive sensor required for on-line analysis. However, its off-line analysis is time-consuming. An on-line COD estimation method was developed with photoelectrocatalytic (PEC) technology. Based on the on-line data of the oxidation-reduction potential (ORP), dissolved oxygen (DO) and pH of wastewater, four different artificial neural network methods were applied to develop working models for COD estimation. Six different batches of sequence batch reactor (SBR) effluent from a paper mill were treated with PEC oxidation for 90 minutes, and 546 data points were collected from the on-line measurements of ORP, DO and pH, and the off-line COD analysis. After having training and validation with 75% and 25% of data, and evaluation with four statistical criteria (R 2 , RMSE, MAE and MAPE), the estimation results indicated that the developed radial basis neural network (RBNN) model demonstrated the highest precision. Subsequently, the application of the RBNN model to a new batch of SBR effluent from the paper mill revealed that the RBNN model was acceptable for COD estimation during the PEC advanced treatment process of papermaking wastewater, which implied its possible application in the future.

Crotamiton, a scabicide and antipruritic agent persistent during biological treatment processes, is frequently detected in secondary effluent. In this study, titanium dioxide (TiO 2 ) and high-silica zeolite (HSZ-385) composites were synthesized and applied for the treatment of crotamiton in secondary effluent. Crotamiton was rapidly adsorbed by HSZ-385, and the adsorption performance of crotamiton in the secondary effluent was quite close to that in the test using ultrapure water. Even though the TiO 2 -zeolite composites showed lower adsorption rates than that of HSZ-385, similar crotamiton adsorption capacities were revealed using both test materials. The photocatalytic decomposition of crotamiton was significantly inhibited by the water matrix at low initial concentrations. The TiO 2 -zeolite composites rapidly adsorbed crotamiton from secondary effluent, and then the crotamiton was gradually decomposed under ultraviolet irradiation. Importantly, when using TiO 2 -zeolite composites, coexisting material in the secondary effluent did not markedly inhibit crotamiton removal at low initial crotamiton concentration. The behaviors of the main intermediates during treatment demonstrated that the main degradation intermediates of crotamiton were also captured by the composites.

In this study, surfactant modified zeolite-clinoptilolite (SMZ) by CPB (cetylpyridinium bromide) was used for simultaneous removal of ammonium, nitrate and phosphate in synthetic wastewater, and the sorption properties of SMZ were determined and compared with natural zeolite. Results showed that natural clinoptilolite had good affinity for ammonium (8.940 mg/g), but not for nitrate (0.427 mg/g) and phosphate (0.801 mg/g). With the increase of surfactant loading from 5 g/L to 40 g/L, the sorption capacity for nitrate increased from 0.462 mg/g to 4.661 mg/g. when the surfactant loading is 40 g/L, the SMZ has a phosphate adsorption capacity of 2.119 mg/g. The SMZ had a significant enhancement on nitrate and phosphate sorption, could simultaneously remove ammonium, nitrate and phosphate at specific conditions, with removal efficiency up to 85.2%, 83.1% and 56.7%, respectively. Orthogonal experiments showed that ammonium concentration was the most important factor for ammonium sorption on SMZ. Surfactant loading was the major factor for nitrate and phosphate sorption. With the increase of surfactant loading from 5 g/L to 40 g/L, the sorption capacity for nitrate increased from 0.462 mg/g to 4.661 mg/g. When the surfactant loading is 40 g/L, the SMZ has the best phosphate adsorption capacity 2.119 mg/g. Samples were characterized by X-ray diffraction (XRD) and Brunauer-Emmett-Teller (BET). Semi-empirical quantum mechanics molecular simulation indicated that electrostatic attraction existed between CPB and dihydrogen phosphate ion. Results indicate that SMZs might have great potential of removing cations and anions simultaneously in the aquatic environment, which is good for eutrophication control and nutrients removal.

Hydrophilic inks have been widely used due to higher printing speed, competitive cost and being healthy non-organic solvents. However, they cause problems in both product quality and process runnability due to their hydrophilic surface wettability, strong negative surface charge and sub-micron size. Electric treatment was shown to be able to increase the ink sizes from 60 nm to 700 nm through electrocoagulation and electrophoresis. In addition, electric treatment assisted flotation could reduce effective residual ink concentration (ERIC) by 90 ppm, compared with only 20 ppm by traditional flotation. Furthermore, the effect of electric treatment alone on ink separation was investigated by two anode materials, graphite and stainless steel. Both of them could remove hydrophilic inks with less than 1% yield loss via electroflotation and electrophoresis. But graphite is a better material as the anode because graphite reduced ERIC by an additional 100 ppm. The yield loss of flotation following electric treatment was also lower by 17% if graphite was the anode material. The difference between the two electrode materials resulted from electrocoagulation and ink redeposition during electric treatment. An electric pretreatment-flotation-hyperwashing process was conducted to understand the deinking performance in conditions similar to a paper mill, and the ERIC was reduced from 950 ppm to less than 400 ppm.

To provide a theoretical basis for alpine source lake protection, ten samples were taken from each lake annually from 2012 to 2015. Each year, the various species of nitrogen and phosphorus nutrients were measured. The average contents of nitrate nitrogen, ammonia nitrogen, nitrite nitrogen, total phosphorus, and total nitrogen in the four lakes are 0.195-0.0 mg/L, 0.038-0.143 mg/L, 0.004-0.168 mg/L, 0.006-0.740 mg/L, and 0.050-0.547 mg/L, respectively. The total phosphorus contents in Eling Lake, Longbao Lake and Sea Star were higher than Class I water quality standards, and the total nitrogen contents in Eling Lake, Sea Star and Zhaling Lake were higher than Class I water quality standards as well. The concentration contour maps of the nitrate nitrogen, ammonia nitrogen, nitrite nitrogen, total phosphorus and total nitrogen showed that the indicators of the four lakes in the east, the west, and the center of the lake did not have the same trend. From 2012 to 2015, each of the measured nutrients showed a rising trend year by year. The four lakes are polluted by both endogenous and exogenous pollution, and it is necessary to limit the exogenous pollution and protect the alpine lakes immediately.

This study prepared a carboxylate-functionalized sugarcane bagasse (CF-SCB) from sugarcane bagasse (SCB) via a simple and low-toxicity chemical modification to enhance its capacity for adsorbing methylene blue (MB) from aqueous solutions. The success of chemical modification was confirmed by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), the pore area and porosity, and zeta potential measurement analysis. The adsorption capacity of CF-SCB was investigated at different pHs, ionic strengths, temperatures, contact times and initial dye concentrations. Equilibrium data were best described by the Langmuir isotherm model, and the maximum monolayer adsorption capacity of CF-SCB (296.74 mg g -1 ) was greatly improved compared with SCB (77.16 mg g -1 ) at 30 °C. The thermodynamic study indicated that MB adsorption onto CF-SCB was a spontaneous, endothermic and entropy increased process. Adsorption kinetics followed a pseudo-second-order mode, and the adsorption mechanism was based on electrostatic interactions. The reusability study showed that CF-SCB had reasonably good reuse potential. All the results suggested that CF-SCB has high potential to be used as an effective and renewable adsorbent for MB removal from wastewater.

A composite coagulant polyferric magnesium silicate (PFMSi) was synthesized by co-polymerization. The structure and morphology of PFMSi were characterized by X-ray diffraction, Fourier transform infrared spectra and scanning electron microscope microphotographs; meanwhile, the coagulation efficiency was evaluated under different ratios of Fe/Si, Mg/Si, basicity ([OH]/[M] ratio), and dosage. The results suggested that the PFMSi coagulant shows an amorphous phase structure, and new chemical compounds had been formed; simultaneously, the different preparation conditions had major effects on coagulation performance. Additionally, the raw water collected from Pearl River was used as a treated water sample to verify the coagulation efficiency of PFMSi. Overall, it is suggested that PFMSi is an efficient coagulant in the removal of turbidity, UV 254 and total organic carbon, and it shows a markedly better coagulation performance than polymeric aluminium and non-modified coagulant. The study of coagulation kinetics and zeta potential showed that adsorption-bridging was the main mechanism for the introduction of silicon.

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.

Microstickies deposits on both paper machine and paper products when it agglomerates under step change in ionic strength, pH, temperature and chemical additives. These stickies increase the down time of the paper mill and decrease the quality of paper. The key property of microstickies is its smaller size, which leads to low removal efficiency and difficulties in measurement. Thus the increase of microstickies size help improve both removal efficiency and reduce measurement difficulty. In this paper, a new agglomeration technology based on electric field was investigated. The electric treatment could also increase the size of stickies particles by around 100 times. The synergetic effect between electric field treatment and detacky chemicals/dispersants, including polyvinyl alcohol, poly(diallylmethylammonium chloride) and lignosulfonate, was also studied.

Ethylenediaminetetraacetic acid (EDTA) forms stable complexes with toxic metals such as nickel due to its strong chelation. The electro-Fenton (EF) process using a cathode made from palladium (Pd), reduced graphene oxide (RGO) and carbon felt, fed with air, exhibited high activities and stability for the removal of 10 mg L(-1) EDTA-Ni solution. Pd/RGO catalyst was prepared by one-pot synthesis; the scanning electron microscopy and X-ray diffraction analysis indicated nanoparticles and RGO were well distributed on carbon felt, forming three dimensional architecture with both large macropores and a mesoporous structure. The cyclic voltammetric results showed that the presence of RGO in Pd/RGO/carbon felt significantly increased the current response of two-electron reduction of O2 (0.45 V). The key factors influencing the removal efficiency of EDTA-Ni, such as pH, current and Fe(2+) concentration, were investigated. Under the optimum conditions, the removal efficiency of EDTA-Ni reached 83.8% after 100 min EF treatment. Mechanism analysis indicated that the introduction of RGO in Pd/RGO/carbon felt significantly enhanced the electrocatalytic activities by inducing •OH in the EF process; direct H2O2 oxidation still accounted for a large amount of EDTA-Ni removal efficiency.

The combination of nitrogen recovery and pharmaceutical removal processes for livestock urine treatment were investigated to suppress the discharge of pollutants and recover nitrogen as resources. We combined methylene urea synthesis from urea and adsorption and photocatalytic decomposition of sulfonamide antibiotic using rotating advanced oxidation contactor (RAOC) contained for obtaining both safe fertilizer and reclaimed water. The methylene urea synthesis could recover urea in synthetic urine, however, almost all sulfonamide antibiotic was also incorporated, which is unfavorable from a safety aspect if the methylene urea is to be used as fertilizer. Conversely, RAOC could remove sulfonamide antibiotic without consuming urea. It was also confirmed that the methylene urea could be synthesized from synthetic urine treated by RAOC. Thus, we concluded that RAOC should be inserted prior to the nitrogen recovery process for effective treatment of urine and safe use of methylene urea as fertilizer.

Attempts were made in this study to examine the efficiency of electrocoagulation (EC) using aluminum (Al) anode and stainless steel net cathode combined with electrochemical oxidation with a β-PbO₂anode or a mixed metal oxide (MMO) anode for treatment of papermaking tobacco sheet wastewater, which has the characteristics of high content of suspended solids (SS), intensive color, and low biodegradability. The wastewater was first subjected to the EC process under 40 mA/cm² of current density, 2.5 g/L of NaCl, and maintaining the original pH of wastewater. After 6 minutes of EC process, the effluent was further treated by electrochemical oxidation. The results revealed that the removal of SS during the EC process was very beneficial to mass transfer of organics during electrochemical oxidation. After the combined process, 83.9% and 82.8% of chemical oxygen demand (COD) removal could be achieved on the β-PbO₂and MMO anodes, respectively. The main components of the final effluent were biodegradable organic acids, such as acetic acid, propionic acid, butyric acid, valeric acid, and hexahyl carbonic acid; the 5-day biochemical oxygen demand/chemical oxygen demand (BOD₅/COD) ratio increased from 0.06 to 0.85 (Al + β-PbO₂) or 0.80 (Al + MMO). Therefore, this integrated process is a promising alternative for pretreatment of papermaking tobacco sheet wastewater prior to biological treatment.

Ultraviolet (UV) light emitting diodes (LEDs) may be a viable option as a UV light source for advanced oxidation processes (AOPs) utilizing photocatalysts or oxidizing agents such as hydrogen peroxide. The effect of UV-LED duty cycle, expressed as the percentage of time the LED is powered, was investigated in an AOP with hydrogen peroxide, using methylene blue (MB) to assess contaminant degradation. The UV-LED AOP degraded the MB at all duty cycles. However, adsorption of MB onto the LED emitting surface caused a linear decline in reactor performance over time. With regard to the effect of duty cycle, the observed rate constant of MB degradation, after being adjusted to account for the duty cycle, was greater for 5 and 10% duty cycles than higher duty cycles, providing a value approximately 160% higher at 5% duty cycle than continuous operation. This increase in adjusted rate constant at low duty cycles, as well as contaminant fouling of the LED surface, may impact design and operational considerations for pulsed UV-LED AOP systems.