This review is intended to evaluate the use of ferrate (Fe(VI)), being a green coagulant, sustainable and reactive oxidant, to remove micro pollutants especially pharmaceutical pollutants in contaminated water. After a brief description of advanced oxidation processes, fundamental dimensions regarding the nature, reactivity, and chemistry of this oxidant are summarized. The degradation of contaminants by Fe(VI) involves several mechanisms and reactive agents which are critically evaluated. The efficiency and chemistry of Fe(VI) oxidation differs according to the reaction conditions and activation agent, such as soluble Fe(VI) processes, which involve Fe(VI), UV light, and electro-Fe(VI) oxidation. Fe(VI) application methods (including single dose, multiple doses, chitosan coating etc), and Fe(VI) with activating agents (including sulfite, thiosulfate, and UV) are also described to degrade the micro pollutants. Besides, application of Fe(VI) to remove pharmaceuticals in wastewater are intensely studied. Electrochemical prepared Fe(VI) has more wide application than wet oxidation method. Meanwhile, we elaborated Fe(VI) performance, limitations, and proposed innovative aspects to improve its stability, such as the generation of Fe(III), synergetic effects, nanopores entrapment, and nanopores capsules. This study provides conclusive direction for synergetic oxidative technique to degrade the micro pollutants.

The reactivity characteristics of humic acid (HA) with aluminium coagulants at different pH values was investigated. It revealed that the linear complexation reaction occurred between aluminum and humic acid at pH < 7, and the reaction rate increased as the pH increased from 2 to 6. While at pH = 7, most of the dosed aluminum existed in the form of free aluminum and remained unreacted in the presence of HA until the concentration reached to trigger Al(OH)₃₍ₛ₎ formation. Differentiating the change of functional groups of HA by ¹H nuclear magnetic resonance spectroscopy and X-ray photoelectron spectra analysis, it elucidated that there was a selective complexation between HA and Al with lower Al dosage at pH 5, which was probably due to coordination of the activated functional groups onto aluminium. While almost all components were removed proportionally by sweep adsorption without selectivity at pH 7, as well as that with higher Al dosage at pH 5. This study provided a promising pathway to analyse the mechanism of the interaction between HA and metal coagulants in future.

With the extensive application of graphene oxide (GO), it is noticeable that part of GO is directly/indirectly released into the environment and widespread research indicated that it had adverse influences on human health and ecological balance. In this work, a novel nanobelt-like Ca/Al layered double hydroxides (CA-LDH) was synthesized and applied as efficient coagulant for the removal of GO from aqueous solutions. The results indicated that neutral pH, co-existing cations and higher temperature were beneficial to the coagulation of GO. The sequence of cation effect for promoting of GO coagulation was Ca2+ > Mg2+ > K+ > Na+, whereas the effect of anions on GO coagulation was PO43− > CO32− > SO42− > Cl−. Comparing with anions, the cations showed more dominate effect for GO coagulation than anions. Hydrogen bonds and electrostatic interaction were the main coagulation mechanisms for GO coagulation, which were evidenced by FT-IR and XPS analysis. Specifically, for the first time, the reclaimed product of CA-LDH after GO coagulation (CA-LDH + GO) was applied as adsorbents for the secondary application in the removal of heavy metal ions from aqueous solutions. Interestingly, the CA-LDH + GO still had high adsorption capacities, i.e., the maximum adsorption capacities (qmax) for Cu(II), Pb(II), and Cr(VI) were 122.7 mg/g, 221.2 mg/g and 64.4 mg/g, respectively, higher than other similar materials. This paper highlighted the LDH-based nanomaterials are promising materials for the elimination of environmental pollutants and the migration and transformation of carbon nanomaterials in the natural environment.

With the development and application of graphene oxides (GO), the potential toxicity and environmental behavior of GO has become one of the most forefront environmental problems. Herein, a novel nanoscale layered double hydroxides (glycerinum-modified nanocrystallined Mg/Al layered double hydroxides, LDH-Gl), layered double oxides (calcined LDH-Gl, LDO-Gl) and metallic oxide (TiO2) were synthesized and applied as superior coagulants for the efficient removal of GO from aqueous solutions. Coagulation of GO as a function of coagulant contents, pH, ionic strength, GO contents, temperature and co-existing ions were studied and compared, and the results showed that the maximum coagulation capacities of GO were LDO-Gl (448.3 mg g−1) > TiO2 (365.7 mg g−1) > LDH-Gl (339.1 mg g−1) at pH 5.5, which were significantly higher than those of bentonite, Al2O3, CaCl2 or other natural materials due to their stronger reaction active and interfacial effect. The presence of SO32− and HCO3− inhibited the coagulation of GO on LDH-Gl and LDO-Gl significantly, while other cations (K+, Mg2+, Ca2+, Ni2+, Al3+) or anion (Cl−) had slightly effect on GO coagulation. The interaction mechanism of GO coagulation on LDO-Gl and TiO2 might due to the electrostatic interactions and strong surface complexation, while the main driving force of GO coagulation on LDH-Gl might be attributed to electrostatic interaction and hydrogen bond, which were further evidenced by TEM, SEM, FT-IR and XRD analysis. The results of natural environmental simulation showed that LDO-Gl, TiO2 or other kinds of natural metallic oxides could be superior coagulants for the efficient elimination of GO or other toxic nanomaterials from aqueous solutions in real environmental pollution cleanup.

In the present work, low-cost and efficient iron oxide nanoparticle incorporated on mesoporous biochar was prepared from effluent treatment plant (ETP) sludge collected from the textile industry. This sludge contains a higher amount of Fe due to the use of ferric chloride as a coagulant in the treatment of wastewater generated during the process. The raw sludge and prepared biochar was extensively examined by various sophisticated techniques like XRF, XRD, BET, TGA, XPS, RAMAN, FTIR, FESEM, TEM, and VSM. TEM and XRD analysis confirms the presence of iron oxide nanoparticles on mesoporous biochar. The prepared biochar was found to possess BET surface area of 91 m² g⁻¹. Several parameters like pH, dose, initial concentration, temperature and time were optimized for the adsorptive removal of ofloxacin (OFL) from aqueous solution. Biochar (named as BTSFe) achieved ≈96% removal efficiency of OFL with a maximum adsorption capacity (qₘ) of 19.74 mg g⁻¹ at optimum condition. π-π electron–donor-acceptor and H bonding were the major mechanisms responsible for the OFL adsorption. Kinetic and equilibrium thermodynamic study of showed that the adsorption of OFL was represented by the pseudo-second-order kinetics model, and the process was exothermic and spontaneous. Additionally, Redlich-Peterson and Freundlich isotherms best fitted the experimental data indicating multilayer adsorption phenomenon. Biochar was magnetically separated and thermally regenerated after each cycle for five times with a nominal overall decrease of ≈8% in removal efficiency. Leaching of iron during the adsorption process was also checked and found to be within the permissible limit. This study provides an alternative application of the textile industry sludge as an efficient, low-cost biochar for the removal of emerging pharmaceutical compounds.

PURPOSE OF REVIEW: The use of conventional chemical coagulant in treatment of wastewater is gaining great attention. Drawbacks related to the prolonged effects on human health and environment due to the generation of by-product non-biodegradable sludge are becoming the latest topics. Transition from chemical to natural coagulant can be a good strategy to reduce the aforementioned drawbacks. Therefore, this review aims to provide critical discussions on the use of natural coagulant along with the comparative evaluation over the chemical coagulant. RECENT FINDINGS: Treatment performances by chemical and natural coagulant have been reviewed on various types of wastewater with different success rates. Based on this review, a transition from the use of chemical to natural coagulant is highly suggested as the performance of the natural coagulant is comparable to that of the chemical coagulant and in some cases even better. The comparative advantages and disadvantages also convinced that the natural coagulant stands a great chance to be used as an alternative over the chemical coagulant. Though the current utilization of natural coagulant is encouraging, three main aspects were overlooked by researchers: active coagulant agent, extraction, and optimization due to different wastewater characteristics. Furthermore, delving into these aspects could clarify the uncertainties on the natural coagulant. Hence, it makes this transition a prospect of green technology with sustainable application towards wastewater treatment.

The textile industry stands out as one of the largest consumers of water among the industrial sectors. Additionally, its effluent presents characteristics such as high load of chemical oxygen demand (COD), total organic carbon (TOC), suspended solids, color, turbidity, phenol, and salts, which require an efficient treatment of the wastewater produced. Among the several researches that have arisen focused on the treatment of textile effluents, electrocoagulation stands out. This method consists of an electrochemical process that generates its own coagulant by applying electric current to metal electrodes immersed in the solution. The electrodes used in the present study are metallic plates made of scrap iron. The objective of this work is to evaluate their application in an electrocoagulation process for the decolorization of real and synthetic effluents. The efficiency of the treatment was evaluated by applying it to a synthetic effluent containing commercial indigo blue dye and to a real effluent from the textile industry, assessing parameters such as color, turbidity, pH, electrical conductivity, COD, TOC, phenol, soluble iron, sludge generation, and electrode wear. The synthetic effluent obtained average color removal of 95%, 96% phenol, and low sludge production in 120 min of electrolysis. In the real effluent from the textile industry, an average color removal of 92%, 97% turbidity, 100% phenol, 65% TOC, and 49% COD in 90 min of electrolysis was obtained. The electrocoagulation process using scrap iron as electrodes proved to be efficient in removing the dye present in the real textile industry effluent, as well as in the synthetic effluent.

It was aimed to precisely investigate the coagulation properties of graphene oxide (GO) as a novel coagulant for turbidity removal from water. For this purpose, the process was simulated through response surface methodology (RSM) to determine the effect of the preselected independent factors (pH, GO dosage, and initial turbidity) and their interaction effects on the process. Based on the results, increased turbidity removal efficiencies were obtained as pH decreased from 10 to 3. Besides, increase of GO dosage within the test range (2.5–30 mg/L) was highly beneficial for enhancing the process performance. However, a slight overdosing of GO was observed for dosages of more than 20 mg/L under pH values of less than about 4. For initial turbidity with test range of 25–300 NTU, there was an optimum range (approximately 120–200 NTU) out of which the removal efficiency declined. According to the results of the analysis of variance (ANOVA), pH and GO dosage, orderly, had the strongest individual effect on the process performance. The most significant interaction effect was also observed between pH and GO dosage. The optimal coagulation conditions with GO dosage of 4.0 mg/L, pH of 3.0, and initial turbidity of 193.34 NTU led to a turbidity removal efficiency of about 98.3%, which was in good agreement with RSM results. Under basic pH levels, the sweeping effect was recognized as the main coagulation mechanism occurred between the negatively surface charged particles of GO and soil. However, according to zeta potential (ZP) analysis results, under acidic pH conditions in addition to the sweep coagulation, the electric double layer compression, and the subsequent ZP reduction also contributed significantly to the process. Scanning electron microscopy (SEM) images showed that the layered structure of GO particles provided an appropriate platform on which the flocs were formed.

Water and wastewater physicochemical treatments often rely on coagulation and flocculation to generate aggregates adequate for separation. Floc development may be assessed by particle size distribution (PSD) using dynamic light scattering techniques (DLS) available in commercial equipment. The DLS output data, however, often presents high variability, which may hinder comparisons of the aggregation time series for different conditions. The Visibility Graph (VG), a novel approach to be applied within the sanitation context, may be an alternative to disclose properties of these highly oscillatory monitoring results. In this study, after defining ideal shear rates and mixing times for the treatability of high-turbidity test water, we monitored PSD after coagulation using metallic salts (ferric chloride and ferric sulfate) and a natural coagulant (Opuntia cochenillifera). PSD data was converted to visibility networks and measurements were obtained to describe these time series by the VG technique. Although no series patterns were found, the VG approach shed some light onto the PSD through time, but no inferences were scaled to the treatability aspect. The limitations for the VG method in this study are mainly due to the small time series; thus, we endorse that visibility network analysis may be a promising technique within the environmental and sanitation context.

Refractory organic pollutants in tail water of dyeing wastewater treatment have aroused wide concern. Their efficient and cost-effective removal reduced their threat to public health and ecosystem. Herein, a novel short-cut photocatalysis/algal degradation-based hybrid technology was implemented in efficient removal of methylene blue (MB) in simulated tail water using reliable titanium dioxide and common Chlorella pyrenoidosa, and the mechanisms in processes were emphasized. The treatment efficiency was significantly improved via pretreatment before chemical and biological degradation. MB of 79.71% was concentrated as the adsorption of the modified titanium dioxide and the collection of titanium dioxide by inorganic coagulant. The supernatant with low concentration of MB after coagulation was able to be directly treated by Chlorella pyrenoidosa. MB of 93.7% was degraded and transformed to intermediates in short-cut photocatalysis under visible light in 1 h. The intermediates owning the low biological inhibition were easily further degraded by Chlorella pyrenoidosa in 6 days. Mechanism analysis implied that the modified titanium dioxide was not simple monolayer adsorption, and physical adsorption was dominant. The coagulant played an essential role of charge neutralization in collection of the modified titanium dioxide. The removal of photocatalytic intermediates was divided to fast adsorption of Chlorella pyrenoidosa, low desorption in lag period of algae, and gradual biodegradation that accompanied with the increase of algal cell quantity.