Release of PAHs from sediments to seawater under wave: Indoor microcosms and level IV fugacity models.

Estuaries and coasts are located at the land-sea interface, where sediment liquefaction due to strong wave action results in significant material exchange at the sediment-seawater system. Polycyclic aromatic hydrocarbons (PAHs), as organic pollutants, are distributed across various media. Herein, the impact of wave was studied on the release of PAHs through indoor microcosmic experiments combined with a level IV fugacity model. Comparison revealed that the release amount and rate of PAHs during static consolidation stage were minimal, whereas wave action substantially enhanced the release. Particularly the sediments in a liquefied state, the PAHs release in Stage III was 1.55-1.86 times that in Stage II, reaching 84.73 µg/L. The loss of soil strength and strong hydrodynamic effects resulted in a substantial release of PAHs into seawater along with suspended solids. Due to volatility of 2-ring PAHs and difficult desorption of 6-ring PAHs, 3-5-ring PAHs are the main contributors to releases into seawater. The model results also indicated that the three PAHs had different fates in the sediment-seawater system, with sediment serving as an important "reservoir" for benzo[a]pyrene entering seawater, while functioning as both a "sink" and a "source" for pyrene.

Removal of sulfonylurea herbicides with g-C3N4-based photocatalysts: A review.

The accumulation of agricultural chemicals in the environment has become a global concern, of which sulfonylurea herbicides (SUHs) constitute a significant category. Solar-driven photocatalysis is favored for removing organic pollutants due to its high efficiency and environmental friendliness. Graphite carbon nitride (g-C3N4)-based materials with superior catalytic activities and physicochemical stabilities are promising photocatalysts. This review describes the g-C3N4-based materials and their uses in the photocatalytic degradation of SUHs or other organic pollutants with similar structures. First, the fundamentals of g-C3N4-based materials and photocatalytic SUHs degradation are discussed to provide an in-depth understanding of the mechanism for the photocatalytic activity. The ability of different g-C3N4-based materials to photocatalytically degrade SUH-like structures is then discussed and summarized based on different modification strategies (morphology modulation, elemental doping, defect engineering, and heterojunction formations). Meanwhile, the effects of different environmental factors on the photocatalytic performance of g-C3N4-based materials are described. Finally, the major challenges and opportunities of g-C3N4-based materials for the photocatalytic degradation of SUHs are proposed. It is hoped that this review will show the feasibility of photocatalytic degradation of SUHs with g-C3N4-based materials.

A study combining a sediment-seawater microcosm with multimedia fugacity model to evaluate the effect of tidal cycles on polycyclic aromatic hydrocarbon release from sediments.

Estuarine sediments are key storage sites for persistent organic pollutants (POPs), and estuaries are strongly influenced by tides throughout the year. Although much work has been done concerning on POPs release, related questions on tidal action have not been considered in the release process. Herein, polycyclic aromatic hydrocarbons (PAHs) release from sediment to seawater was investigated under tidal action by combining a tidal microcosm with level IV fugacity model. The results showed that PAHs release with tidal action was 2.0-3.5 times the accumulation of that without tidal action. Tidal action was confirmed to influence strongly PAHs release from sediment to seawater. We also quantified suspended substance (SS) in the overlying water, and an obvious positive correlation between the PAHs concentration and SS content was found. In addition, an increase in seawater depth enhanced the intensity of tidal action, and more PAHs were released, especially dissolved PAHs. Moreover, the fugacity model results showed a good fit with the experimental results. The simulated values demonstrated that the PAHs release was accomplished via two processes, "rapid release" and "slow release". And the sediment played a key role in the fate of PAHs and was a major sink in the sediment-seawater system.

Magnetically separable laccase-biochar composite enable highly efficient adsorption-degradation of quinolone antibiotics: Immobilization, removal performance and mechanisms.

The tremendous potential of hybrid technologies for the elimination of quinolone antibiotics has recently attracted considerable attention. This current work prepared a magnetically modified biochar (MBC) immobilized laccase product named LC-MBC through response surface methodology (RSM), and LC-MBC showed an excellent capacity in the removal of norfloxacin (NOR), enrofloxacin (ENR) and moxifloxacin (MFX) from aqueous solution. The superior pH, thermal, storage and operational stability demonstrated by LC-MBC revealed its potential for sustainable application. The removal efficiencies of LC-MBC in the presence of 1 mM 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) for NOR, ENR and MFX were 93.7 %, 65.4 % and 77.0 % at pH 4 and 40 °C after 48 h reaction, respectively, which were 1.2, 1.3 and 1.3 times higher than those of MBC under the same conditions. The synergistic effect of adsorption by MBC and degradation by laccase dominated the removal of quinolone antibiotics by LC-MBC. Pore-filling, electrostatic, hydrophobic, π-π interactions, surface complexation and hydrogen bonding contributed in the adsorption process. The attacks on the quinolone core and piperazine moiety were involved in the degradation process. This study underscored the possibility of immobilization of laccase on biochar for enhanced remediation of quinolone antibiotics-contaminated wastewater. The proposed physical adsorption-biodegradation system (LC-MBC-ABTS) provided a novel perspective for the efficient and sustainable removal of antibiotics in actual wastewater through combined multi-methods.

Biochar composite derived from cellulase hydrolysis apple branch for quinolone antibiotics enhanced removal: Precursor pyrolysis performance, functional group introduction and adsorption mechanisms.

In this study, magnetic biochar (MAB) and humic acid (HA)-coated magnetic biochar produced from apple branches without and after cellulase hydrolysis (HMAB and CHMAB, respectively) were prepared and tested as adsorbents of enrofloxacin (ENR) and moxifloxacin (MFX) in aqueous solution. Compared with MAB and HMAB, novel adsorbent CHMAB possessed a superior mesoporous structure, greater graphitization degree and abundant functional groups. When antibiotic solutions ranged from 2 to 20 mg L-1, the theoretical maximum adsorption capacities of CHMAB for ENR and MFX were 48.3 and 61.5 mg g-1 at 35 °C with adsorbent dosage of 0.4 g L-1, respectively, while those of MAB and HMAB were 39.6 and 54.4 mg g-1, and 44.7 and 59.0 mg g-1, respectively. The pseudo-second-order kinetic model and Langmuir model presented a better fitting to the spontaneous and endothermic adsorption process. The maximum adsorption capacity of ENR and MFX onto CHMAB was achieved at initial pH values of 5 and 8, respectively. Additionally, the adsorption capacity of ENR and MFX decreased with increasing concentrations of K+ and Ca2+ (0.02-0.1 mol L-1). Synergism between the pore-filling effect, π-π electron-donor-acceptor interactions, regular and negative charge-assisted H-bonding, surface complexation, electrostatic interactions and hydrophobic interactions may dominate the adsorption process. This study demonstrated that a novel magnetic biochar composite prepared through pyrolysis of agricultural waste lignocellulose hydrolyzed by cellulase in combination with HA coating was a promising adsorbent for eliminating quinolone antibiotics from aqueous media.

A comprehensive review of capacitive deionization technology with biochar-based electrodes: Biochar-based electrode preparation, deionization mechanism and applications.

The recently developed techniques for desalination and wastewater treatment are costly and unsustainable. Therefore, a cost-effective and sustainable approach is essential to achieve desalination through wastewater treatment. Capacitive deionization (CDI), an electrochemical desalination technology, has been developed as a novel water treatment technology with great potential. The electrode material is one of the key factors that promotes the development of CDI technology and broadens the scope of CDI applications. Biochar-based electrode materials have attracted increasing attention from researchers because of their advantages, such as environmentally friendly, economical, and renewable properties. This paper reviews the methods for preparing biochar-based electrode materials and elaborates on the mechanism of CDI ion storage. We then summarize the applications of CDI technology in water treatment, analyze the mechanism of pollutant removal and resource recovery, and discuss the applicability of different CDI configurations, including hybrid CDI systems. In addition, the paper notes that environmentally friendly green activators that facilitate the development of pore structure should be developed more often to avoid the adverse environmental impact. The development of ion-selective electrode materials should be enhanced and it is necessary to comprehensively assess the impact of heteroatoms on selective ion removal and CDI performance. Electrooxidation of organic pollutants should be further promoted to achieve organic degradation by extending to redox reactions.

Effect of Pretreatment on Hydraulic Performance of the Integrated Membrane Process for Concentrating Nutrient in Biogas Digestate from Swine Manure.

Nanofiltration (NF) or reverse osmosis (RO) process has been widely applied for concentrating nutrient in biogas digestate. However, efficient pretreatment is key to the sustainable operation of NF or RO. In this study, the combination of NF and RO for concentrating biogas digestate was compared using different pretreatments of hollow fiber ultrafiltration membrane (HFUFM) and ceramic membrane (CUFM). Pilot-scale batch tests were conducted (500 L). CUFM showed a higher membrane flux than HFUFM (100 ~ 180 L·(m2·h)-1 vs. 17 ~ 35 L·(m2·h)-1), but they showed little impact on the NF + RO process. Membrane fluxes of NF and RO were 20 ~ 48 L·(m2·h)-1 and 16 ~ 40 L·(m2·h)-1, respectively. In the RO permeates, the removal rates of total suspended solids (TSS), total solids (TS), chemical oxygen demand (COD), total nitrogen (TN), NH4+-N, and Cl- were above 91%. In the concentrates, TN and total potassium (TK) were concentrated by 1.60 and 2.00 folds in the NF stage, and by 2.10 and 2.30 folds in the RO stage. Further attention should be paid to the antibiotics risks in the concentrates before they are utilized as plant fertilizers.

Optimization of Ammonia Stripping of Piggery Biogas Slurry by Response Surface Methodology.

Ammonia stripping is a pretreatment method for piggery biogas slurry, and the effectiveness of the method is affected by many factors. Based on the results of single-factor experiments, response surface methodology is adopted to establish a quadratic polynomial mathematical model relating stripping time, pH value and gas flow rate to the average removal rate of ammonia nitrogen to explore the interactions among various influencing factors, obtain optimized combined parameters for ammonia stripping, and carry out experimental verification of the parameters. The results show that when hollow polyhedral packing is adopted under operating conditions including a stripping time of 90 min, pH value of 11, gas flow rate of 28 m3/h, gas-liquid ratio of 2000 and temperature of 30 °C, the average removal rate of ammonia nitrogen in biogas slurry can reach approximately 73%. The experimental value is only 4.2% different from the predicted value, which indicates that analysis on the interaction among factors influencing ammonia stripping of biogas slurry and parameter optimization of the regression model are accurate and effective.