Sewage sludge has been regarded as an economic and efficient soil amendment for mudflat soil amendment despite of the concern of heavy metal contamination. Converting sewage sludge into vermicompost by earthworms may be effective to minimize the risk of heavy metal contamination caused by direct application of sewage sludge in mudflat soil. The objective of this study was to assess the feasibility of vermicompost amendment (VA), and its influence on heavy metal contamination compared with sewage sludge amendment (SSA) in mudflat soil. The results showed that VA improved the physicochemical properties of mudflat soil by decreasing soil bulk density, salinity, and pH, increasing soil organic carbon, nitrogen, and phosphorus contents in the soil. Consequently, the maize biomass and yield were significantly elevated by VA. For heavy metals, VA increased total Cd, Cu, Ni, Pb, and Zn concentrations in mudflat soil, and the maximum increments occurred at 250 t ha⁻¹. Available Cd, Cu, Mn, Ni, and Zn concentrations significantly increased with increasing VA rates. VA increased the accumulation of Cd, Cu, Mn, Ni, Pb, and Zn in maize tissues, especially in root of maize. Compared with SSA under the condition of maintaining equal carbon input, VA allowed heavy metals to accumulate in a more stable binding form in the top 20-cm layer of mudflat soil. Thus, the risk of runoff and leaching of heavy metals and their bioavailability to plants reduced in mudflat soil. As a result, VA decreased the accumulation of heavy metals in maize plant compared with SSA in mudflat soil. In summary, vermicompost can be an effective and safe substitute for sewage sludge for mudflat amendment.

An in vitro study was conducted to evaluate the effects of thidiazuron (TDZ) growth regulator and magnesium oxide (MgO) nanoparticles on radish (Raphanus sativus L.) under lead (Pb) stress. Effects of TDZ and MgO on seed germination, growth, biomass, total phenolics and flavonoids, antioxidant potential, and Pb phytoaccumulation in different plant parts were assessed. Nanoparticles of MgO were synthesized with leaf extract of Sageretia thea (Osbeck) plant. Thidiazuron and MgO nanoparticles were added to growth media in individual and in combinations. Lead (50 mg L⁻¹) was added to growth media. Thidiazuron and MgO nanoparticles increased plant growth, phenolic and flavonoid contents, free radical scavenging activity, and lead phytoaccumulation. The increase was highly significant in TDZ and MgO nanoparticle combination treatments (T5, T6). Treatment (T6) showed a sixfold increase in Pb accumulation (1721.73 ± 17.4 μg g⁻¹ dry biomass) as compared to control (274.29 ± 4.23 μg⁻¹g⁻¹). Total phenolic and dry biomass showed significantly positive correlation in leaves (R² = 0.73), stem (R² = 0.58), and roots (R² = 0.72). The correlation of Pb accumulation and phenolic contents was significantly positive in root (R² = 0.80), stem (R² = 0.92), and leaves (R² = 0.69). Flavonoid showed a positive correlation with dry biomass and Pb accumulation. Antioxidant activity was highly increased in leaves followed by stem and root. Findings show that TDZ in combination with MgO nanoparticles can play a significant role in secondary metabolite production and Pb phytoaccumulation.

A regional raw clay was used as the starting material to prepare iron-pillared clays with different iron contents. The catalytic activity of these materials was tested in the heterogeneous photo-Fenton process, applied to the degradation of 2-chlorophenol chosen as the model pollutant. Different catalyst loads between 0.2 and 1.0 g L⁻¹ and pH values between 3.0 and 7.0 were studied. The local volumetric rate of photon absorption (LVRPA) in the reactor was evaluated solving the radiative transfer equation applying the discrete ordinate method and using the optical properties of the catalyst suspensions. The photonic and quantum efficiencies of the 2-chlorophenol degradation depend on both the catalyst load and the iron content of the catalyst. The higher values for these parameters, 0.080 mol Einstein⁻¹ and 0.152 mol Einstein⁻¹, respectively, were obtained with 1.0 g L⁻¹ of the catalyst with the higher iron content (17.6%). For the mineralization process, photonic and quantum efficiencies depend mainly on the catalyst load. Therefore, it was possible to employ a natural and cheap resource from the region to obtain pillared clay-based catalysts to degrade organic pollutants in water.

In this study, thermochemical degradation of furfural by sulfate radical has been investigated to find the best-operating conditions. For this purpose, the response surface methodology (RSM) based on central composite design (CCD) was applied to optimize the five independent variables of thermally activated persulfate (TAP)/nZVI oxidation process including pH, PS concentration, furfural concentration, nZVI dosage, and heat. The ANOVA results (“P > F value” < 0.0001 and [Formula: see text] = 0.9701) showed the obtained quadratic model is acceptable to predict furfural removal. Based on the reduced quadratic model PS concentration, nZVI dosage, and heat revealed the positive effects on removal efficiency, while pH and furfural concentration had a negative effect. Accordingly, 98.4% of furfural could be removed within 60 min of reaction under the optimum conditions: pH 5.26, PS concentration of 20.52 mM, furfural concentration of 84.32 mg/L, nZVI dosage of 1.15 mg/L, and a temperature of 79 °C. In such circumstances, the furfural removal efficiency for TAP, PS/nZVI, PS, and nZVI was 94.5, 9, 3, and 2%, respectively. Therefore, based on the synergy index (SI) values, the combination of PS, nZVI, and heat can lead to a synergistic effect in the performance of the thermochemical process.

A novel magnetic bio-adsorbent was prepared from the leaves of Aegle marmelos tree (Indian bael) and Fe₂O₃ nanoparticles. The AMP@Fe₂O₃ nanocomposite (Aegle marmelos leaf powder) was synthesized by pyrolysis process and applied for As(V) removal through batch adsorption process. The synthesized AMP@Fe₂O₃ nanocomposite was analyzed by several instrumental techniques like XRD, FESEM, TEM, HRTEM, FTIR, BET, and VSM studies. Maximum amount of As(V) was removed at pH 3, contact time of 250 min, adsorbent dose of 0.1 g/L, and initial concentration of 0.5 mg/L at room temperature. The model study revealed that the pseudo-second-order kinetics and Langmuir isotherm models were best fitted with the experimental data. The nanocomposite showed a maximum adsorption capacity of 69.65 mg/g. The endothermic nature of the adsorption process was ascertained from the thermodynamics studies. The zeta potential and FTIR analysis before and after adsorption demonstrated two types of adsorption mechanism. The first one was the electrostatic attraction between negatively charged As(V) ions (H₂AsO₄⁻) and protonated −OH group present on the Fe₂O₃ surface and the second one was ligand exchange between the surface hydroxyl groups and As(V) ions. The AMP@Fe₂O₃ nanocomposite was desorbed with 0.5 M NaOH solutions and also used up to four cycles without any major decrease in removal efficiency. Thus, AMP@Fe₂O₃ nanocomposite can be applied as a potential adsorbent for As(V) removal from wastewater.

In this research, we conducted a statistical analysis of ten (metalloid) heavy metals, including Cu, Hg, Cd, Zn, Pb, As, Ni, Cr, Co, and Mn in urban dust of 58 cities in China from 2000 to 2018, and then we analyzed the statistic characters, pollution statue, and health risks of ten heavy metals. Results showed that (1) the maximum (average) values of ten (metalloid) heavy metals in the street dust of 58 Chinese cities all exceeded Chinese background values, and there were obvious differences in contents of heavy metals of Hg, Zn, Co, Cr, and As between industry cities and common cities. A provincial spatial distribution analysis revealed large variations of distributions of heavy metals Cu, Zn, Pb, and Cr, which distributed in cities mainly located in southern, central, and eastern China, ranging from relatively low to high levels, while Ni, Co, and Mn mainly distributed in southern and central China. This is mainly associated with the mining of the cities. (2) Igₑₒ analysis showed that there was no obvious Ni, Mn, or Co pollution in street dust, while the other tested heavy metals had a range of low to high levels of pollution, in particular, seven metals among them had low to extremely strong levels of pollution (Igₑₒ values between 0 and 7.154), and the average Igₑₒ values were in the following order: Cd > Hg > Zn > Pb > Cu > As>Cr > Mn > Co > Ni. (3) Health risks evaluation showed that of the three exposure ways, the HQᵢₙg from hand-mouth intake was the most common exposure route for both children and adults, especially for children, followed by skin absorption and respiration ways. This research showed that the HI value for children was higher than 1, indicative of no carcinogenic risks, while the HI values for both male and female were lower than 1, indicative of carcinogenic risks; calculation of carcinogenic risk through respiratory route showed that the risks of five elements were within the range 10⁻⁶–10⁻⁴, indicative of carcinogenic risk, among which Cr accounting exceeded 90% of total, which needs to be paid more attention to.

Internal micro-electrolysis (IE) coupled with Fenton oxidation (IEF) was a very effective technology for copper (Cu)–ethylenediaminetetraacetic acid (EDTA) wastewater treatment. However, the mechanisms of Cu²⁺ removal and EDTA degradation were scarce and lack persuasion in the IEF process. In this paper, the decomplexation and removal efficiency of Cu–EDTA and the corresponding mechanisms during the IEF process were investigated by batch test. An empirical equation and the oxidation reduction potential (ORP) index were proposed to flexibly control IE and the Fenton process, respectively. The results showed that Cu²⁺, total organic carbon (TOC), and EDTA removal efficiencies were 99.6, 80.3, and 83.4%, respectively, under the proper operation conditions of iron dosage of 30 g/L, Fe/C of 3/1, initial pH of 3.0, Fe²⁺/H₂O₂ molar ratio of 1/4, and reaction time of 20 min, respectively for IE and the Fenton process. The contributions of IE and Fenton to Cu²⁺ removal were 91.2 and 8.4%, respectively, and those to TOC and EDTA removal were 23.3, 25.1, and 57, 58.3%, respectively. It was found that Fe²⁺-based replacement–precipitation and hydroxyl radical (•OH) were the most important effects during the IEF process. •OH played an important role in the degradation of EDTA, whose yield and productive rate were 3.13 mg/L and 0.157 mg/(L min⁻¹), respectively. Based on the intermediates detected by GC-MS, including acetic acid, propionic acid, pentanoic acid, amino acetic acid, 3-(diethylamino)-1,2-propanediol, and nitrilotriacetic acid (NTA), a possible degradation pathway of Cu–EDTA in the IEF process was proposed. Graphical abstract The mechanism diagram of IEF process

Effect of mechanical scouring driven by granular activated carbon (GAC) fluidization on membrane fouling was investigated using a laboratory-scaled, fluidized membrane reactor filtering the effluent from anaerobic fluidized bed bioreactor (AFBR) in domestic wastewater treatment. The GAC particles were fluidized by recirculating a bulk solution only through the membrane reactor to control membrane fouling. The membrane fouling was compared with two different feed solutions, effluent taken from a pilot-scaled, AFBR treating domestic wastewater and its filtrate through 0.1-μm membrane pore size. The GAC fluidization driven by bulk recirculation through the membrane reactor was very effective to reduce membrane fouling. Membrane scouring under GAC fluidization decreased reversible fouling resistance effectively. Fouling mitigation was more pronounced with bigger GAC particles than smaller ones as fluidized media. Regardless of the fluidized GAC sizes, however, there was limited effect on controlling irreversible fouling caused by colloidal materials which is smaller than 0.1 μm. In addition, the deposit of GAC particles that ranged from 180 to 500 μm in size on membrane surface was very significant and accelerated fouling rate. Biopolymers rejected by the membranes were thought to play a role as binding these small GAC particles on membrane surface strongly.

Although plastic induces environmental damages, almost the consumption of poly(vinyl chloride) never stops increasing. Therefore, this work abstracted by two parts, first, synthesis of Schiff bases 1–4 compounds through the reaction of amino group with appropriate aromatic aldehyde, reaction of PVC with Schiff bases compounds 1–4 in THF to form a new modified PVC-1, PVC-2, PVC-3, and PVC-4. The structures of Schiff bases 1–4 and the modified PVC-1, PVC-2, PVC-3, and PVC-4 have been characterized by different spectroscopic analyses. Second, the influence of introducing 4-amino-1,2,4-triazole as a pendent groups into PVC chain investigated on photostability rules of tests. The modified polymers photostability investigated by observing indices (ICO, Iₚₒ, and IOH), weight loss, UV and morphological studies, and all results obtained indicated that PVC-1, PVC-2, PVC-3 and PVC-4 gave lower growth rate of ICO, IPO, and IOH through UV exposure time. The photostability are given as PVC-4 < PVC-3 < PVC-2 < PVC-1 from different mechanisms which suggested building on existence of 4-amino-1,2,4-triazole moieties in the polymer chain.

Only a small proportion of pharmaceuticals available for commercial use have been monitored in the aquatic environment, and even less is known about the effects on organisms. With thousands of pharmaceuticals in use, it is not feasible to monitor or assess the effects of all of these compounds. Prioritisation schemes allow the ranking of pharmaceuticals based on their potential as environmental contaminants, allowing resources to be appropriately used on those which are most likely to enter the environment and cause greatest harm. Many different types of prioritisation schemes exist in the literature and those utilising predicted environmental concentrations (PECs), the fish plasma model (FPM), critical environmental concentrations (CECs) and acute ecotoxicological data were assessed in the current study using the 50 most prescribed drugs in the UK. PECs were found to be overestimates of mean measured environmental concentrations but mainly underestimations of maximum concentrations. Acute ecological data identified different compounds of concern to the other effects assessments although the FPM and CECs methods were more conservative. These schemes highlighted antidepressants, lipid regulators, antibiotics, antihypertensive compounds and ibuprofen as priority compounds for further study and regulation.