Dye Wastewater Treatment Research Articles

Enhanced Salinity Gradient Energy Conversion by Photodegradable MXene/TiO2 Membrane Utilizing Saline Dye Wastewater

AbstractThe utilization of nanochannel membranes for harvesting salinity gradient energy has shown promising potential in addressing the energy crisis and environmental pollution issues. While previous studies have mainly focused on extracting salinity energy from mixing artificial seawater with river water, the research introduces a creative approach involving dye wastewater treatment using MXene/TiO2 membranes to achieve simultaneous photocatalytic degradation and power generation via salinity gradients. The built‐in electric field generated by MXene/TiO2 heterojunctions enhances ionic transport and electron‐hole separation. After photocatalytic treatment of saline dye wastewater, the membrane is defined as a photodegradable membrane. This membrane exhibits increased surface charge and expanded layer spacing to optimize salinity gradient energy conversion efficiency, yielding an impressive power density of up to 11.78 W m−2, which is 20% higher than that of the original MXene/TiO2 membrane. This work offers valuable insights into the development of multifunctional materials for sustainable power generation that comprehensively utilize industrial wastewater and domestic sewage.

A “self-driven” roving membrane with enhanced water-pumping and dye rejection performance

Considering that traditional membrane treatment of dyeing wastewater requires extra driving pressure, this work successfully prepared a roving membrane powered by the siphoning and wicking effects of the roving to separate dyes from dyeing wastewater. In this work, we found that bamboo pulp roving had the optimal siphoning and wicking performance, making it the focus for subsequent research. At the optimized interfacial polymerization parameters, the prepared roving membrane exhibited the optimal water-pumping and dye rejection performance, which reached 9.11 g/h and 99.58 %, respectively. The diameter of the rovings wrapped in polyamide layer became smaller and the wicking performance was improved. In addition, the thickness of polyamide layer with uniformly distributed nanoTiO2 decreased, and the crosslinking degree was enhanced. Ultraviolet light further contributed to the enhanced water-pumping and dye rejection performance of the piperazine/TiO2/trimesoyl chloride roving membrane. During the 120-h continuous filtration, the water-pumping and rejection performance was stable with only small fluctuations. Importantly, high dye retentions and water-pumping rate were achieved. In this study, we successfully prepared a membrane that is easy to use and does not require extra driving pressure, providing a new approach for dye wastewater treatment.

Synthesis, Magnetic, and Photocatalytic Activity of Polypyrrole-Based TiO2–Fe Catalyst for Wastewater Treatment

The primary aim of this study is to investigate the degradation efficacy of the Ppy/TiO2-Fe photocatalyst for MB dye in an aqueous solution. Firstly, the direct addition of TiO2 and Fe was done to prepare Ppy/TiO2-Fe photocatalyst. Fourier transformation infrared spectroscopy, XRD, SEM, BET surface area analysis, and magnetization tests established the formation of the Ppy/TiO2-Fe photocatalyst. The crystallite sizes of TiO2, Fe-TiO2, and Ppy/TiO2-Fe photocatalyst were estimated to be 24.99 nm, 21.94 nm, and 21.84 nm, respectively. For the synthesis confirmation, the FTIR spectrum confirmed the existence of Ti-O, Fe-O, and Ppy-related bonds. While comparing the SEM images, the impact of polypyrrole on the particle shape was observed with less aggregation and increased surface roughness. The VSM analysis revealed that incorporating polypyrrole (Ppy) into Fe-TiO2 significantly enhances its magnetic properties, with Ppy/TiO2-Fe exhibiting superparamagnetic behavior, characterized by a higher saturation magnetization (Ms) of 33.11 emu/g and a lower coercivity (Hc) of 0.160 Oe, compared to Fe-TiO2’s Ms of 1.09 emu/g and Hc of 341.39 Oe. The N2 sorption desorption, with a specific surface area of 2.25 × 102 m2/g, is beneficial for photocatalytic activity. The concentration of dye, amount of catalyst, pH, and temperature were studied to evaluate the photocatalytic efficiency of the synthesized Ppy/TiO2-Fe photocatalyst under different conditions. The findings revealed a degradation efficiency of 91.92%. The degradation rate reached 91.92% under optimal conditions within 120 min and could be fitted well by first-order kinetics. The photocatalytic efficiency was also evaluated for the scavenger, and the concentration of H2O2 and the reusability of the catalyst were demonstrated. Based on the observed results, the Ppy/TiO2-Fe photocatalyst could be applied more effectively and efficiently to photocatalytic degradation of organic dyes in wastewater treatment.

Optimization, purification and characterization of laccase from a new endophytic Trichoderma harzianum AUMC14897 isolated from Opuntia ficus-indica and its applications in dye decolorization and wastewater treatment.

Hazardous synthetic dye wastes have become a growing threat to the environment and public health. Fungal enzymes are eco-friendly, compatible and cost-effective approachfor diversity of applications. Therefore, this study aimed to screen, optimize fermentation conditions, and characterize laccase from fungal endophyte with elucidating its ability to decolorize several wastewater dyes. A new fungal endophyte capable of laccase-producing was firstly isolated from cladodes of Opuntia ficus-indica and identified as T. harzianum AUMC14897 using ITS-rRNA sequencing analysis. Furthermore, the response surface methodology (RSM) was utilized to optimize several fermentation parameters that increase laccase production. The isolated laccase was purified to 13.79-fold. GFC, SDS-PAGE revealed laccase molecular weight at 72kDa and zymogram analysis elucidated a single band without any isozymes. The peak activity of the pure laccase was detected at 50°C, pH 4.5, with thermal stability up to 50°C and half life span for 4h even after 24h retained 30% of its activity. The Km and Vmax values were 0.1mM, 22.22µmol/min and activation energy (Ea) equal to 5.71kcal/mol. Furthermore, the purified laccase effectively decolorized various synthetic and real wastewater dyes. Subsequently, the new endophytic strain produces high laccase activity that possesses a unique characteristic, it could be an appealing candidate for both environmental and industrial applications.

Exploring performance and mechanism of modified metal-organic frameworks in calcium alginate/polyvinyl alcohol double-network hydrogels for effective dye wastewater treatment

To address the growing problem of dye wastewater pollution, a novel MOFs adsorbent calcium alginate/polyvinyl alcohol@UiO-66 was developed using environmentally friendly polymers, sodium alginate and polyvinyl alcohol creating gel spheres with a double-network structure through cross-linking. UiO-66 metal-organic frameworks are then grown onto the gel spheres, resulting in the final CA/PVA@UiO-66 adsorbent. This adsorbent boasts a high surface area (17.4 m2/g) and a mesoporous-nested microporous structure. It effectively removes MB from water, the actual maximum adsorption capacity was measured at 275.8 mg/g, which surpasses most existing adsorbents. Remarkably, the adsorbent retains 93.9 % of its initial capacity even after 10 reuse cycles. The adsorption process adhered to the Redlich-Peterson model and the PFO model. The N2-Sorption isotherm, actual Methylene blue (MB) adsorption experiments, and model analysis further suggest that the adsorption process is a complex heterogeneous diffusion process involving simultaneous chemical and physical adsorption. Additionally, the adsorption process is endothermic, indicating that it can occur spontaneously at 298 K. Increasing the temperature promotes the forward progress of the adsorption reaction, thereby enhancing the adsorption capacity. The gel adsorbent exhibited excellent dye wastewater purification capabilities, coupled with commendable reusability.

Dye wastewater treatment using nonthermal plasma-treated copper oxide nanoparticles produced through electrolysis technique

Abstract Copper oxide nanoparticles (CuO-NPs) were produced by implementing an electrolysis technique. The prepared CuO-NPs were processed with nonthermal microwave plasma to check the effect of plasma treatment on their morphology and photocatalytic response. The plasma processed and blank CuO-NPs samples were used in dye degradation and water splitting applications under simulated sunlight. The blank sample posed undefined morphology, which turned to spherical particles on plasma processing. The particle size grows slightly with processing time. The blank samples showed a crystallite size of 4.512 nm, which grew to 5.34 nm, 5.40 nm, and 5.49 nm after plasma processing for 10, 20, and 30 min, respectively. The lattice parameter UT sample was measured to be 2.4308 Å, with turned to 3.1091, 3.2112, and 3.3099 after 10, 20, and 30 min of plasma treatment, respectively. Similarly, band gap of CuO-NPs reduced from 2.4 eV to 2.24 eV after plasma processing for 30 min. The porosity of the nanoparticles also showed a similar trend. The plasma processing of CuO-NPs for 30 min produced the best results for photocatalytic water splitting and dye degradation applications. The photocatalytic activity revealed hydrogen evolution of 38.05 mmol.g−1.h−1 and dye removal efficiency of 91%.

Mixed matrix membranes by post-modified UiO-66-NH2 for efficient treatment of dyeing wastewater

The preparation of modified membranes utilizing the UiO-66 framework for wastewater filtration is regarded as one of the most promising approaches to wastewater treatment, owing to its high efficiency and cost-effectiveness. In this study, a post-modified MOF, UiO-66-RSA, was synthesized via the condensation reaction of UiO-66-NH2 and 2,4-dihydroxybenzaldehyde. PVDF mixed matrix membranes (MMMs) were fabricated for the first time by mixing UiO-66-RSA into PVDF using the non-solvent induced phase separation (NIPS) method. Compared to pure PVDF membranes, the newly developed membrane, M4, demonstrated enhanced compatibility and superior mechanical strength. In dyeing wastewater treatment applications, M4 showed excellent separation efficiency for dye and heavy metal mixed wastewater, achieving rejection rates exceeding 90 %. Additionally, it maintained a high flux recovery rate (FRR > 90 %) and rejection rate (Rejection > 90 %) after six filtration cycles of dye-containing wastewater, indicating strong recyclability. These findings suggest that MMMs embedded with UiO-66-RSA hold significant promise for dyeing wastewater treatment.

Micro-nano bubbles in action: AC/TiO2 hybrid photocatalysts for efficient organic pollutant degradation and antibacterial activity

Developing highly active and sustainable photocatalysts is crucial for environmental remediation. This work focuses on the enhanced photocatalytic degradation efficiency of synthetic dyes using TiO2-coated AC hybrid photocatalysts under MNB aeration. The TiO2-coated AC hybrid photocatalyst (HP) was synthesized via a sol-gel method and characterized using XRD, FTIR, SEM, EDS, HR-TEM, and DRS. The study investigated the photocatalytic degradation of three dyes indigo carmine (IC), reactive black 5 (RB5), and methylene blue (MB) in wastewater, with initial dye concentrations ranging from 10 to 100 μM. Under UVA irradiation, the hybrid photocatalyst with MNB aeration (HP + UVA + MNB) achieved the highest degradation efficiencies of 69.09%, 60.06%, and 55.19% for IC, MB, and RB5, respectively. Further analysis showed that the chromophores and complex structures of these dyes were broken into intermediate products. The Langmuir-Hinshelwood kinetic model was used to describe the reaction mechanisms. The HP + UVA + MNB system demonstrated superior photocatalytic degradation activity, making it suitable for operational and environmental applications in dye wastewater treatment. Additionally, the antibacterial properties of AC and HP were tested at 100 μg/mL, showing effectiveness against both Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli.

Vacancy defect and piezoelectric field assisted photocatalytic performance of BiO(Cl1/3Br1/3I1/3)x for the degradation of organic pollutants

Semiconductor photocatalysts have been widely researched in wastewater treatment of organic dyes, among which bismuth halide semiconductors have shown great application prospects due to their unique layered structure and diverse micromorphology. As for photocatalysis, high concentration of photo-generated carriers and their effective separation are considered to be the key to obtain excellent photocatalytic performance. In view of the common issues of high bandgap energy and low carrier separation rate in bismuth halide, in this paper, the BiO(Cl1/3Br1/3I1/3)x catalysts with different proportions of Bi3+ and (Cl1/3Br1/3I1/3)- were designed and synthesized by hydrothermal method, through constructing hybrid energy levels and thus accomplishing by multi-halogen doping to widen the light absorption range. For another, the efficient separation of electrons and holes was achieved in BiO(Cl1/3Br1/3I1/3)x in virtue of a built-in field stemmed from the intrinsic piezoelectric effect, and band tilting. Meanwhile, more active sites were induced by Vo•• and VBiʹʹʹ due to the directional impact of the built-in field. Ultimately, BiO(Cl1/3Br1/3I1/3)5/7 demonstrated the optimum catalytic performance under the combined light irradiation and ultrasonic vibration, with the degradation efficiency of MB reaching 91.28 % in 60 min and the k of 0.0360 min−1, and 97.44 % degradation efficiency of Rh B within 18 min and the k of 0.1565 min−1 together with excellent cycling stability. The prepared BiO(Cl1/3Br1/3I1/3)5/7 catalyst has a huge application potential for the degradation of wastewater, taking full advantage of environmental vibration energy and light energy.

Development of the novel advanced electrooxidation process for decolorization of recalcitrant dyes (Methylene Blue, Rhodamine B, Congo Red): Effect of operating factors

The research aims to develop an advanced electrooxidation process for decolorization of recalcitrant dye. To enhance the radical formation, a combination of UV irradiation and electrooxidation (UV/EO) is used. Methylene Blue (MB), Rhodamine B (RB) and Congo Red (CR) dyes were used as model compounds to represent recalcitrant dyes. The performance of UV/EO process was investigated under various operating factors (i.e., current density (CD), voltage, pH, NaCl, anodic material), and compared with chlorination, UV irradiation, and electrooxidation (EO) process. MB was the highest resistant dye to the UV/EO process. The UV/EO process exhibited a synergistic effect on decolorization, and it removed MB 1.35 time faster than the EO process. Based on indirect determination of •OH, the •OH formation in the EO process was 2.4 ×10−13 M, which lower than that in the UV/EO process by 4 times. The second-order rate constant for MB oxidation by HO• (kHO•,MB) was 3.31 × 109 M−1s−1. The pseudo 1st-order decolorization kinetic (k’) was independent with voltages, but directly depended on CD and NaCl concentrations. Lower pH enhanced the k’ value. The specific energy consumption was in a range of 0.408 – 5.303 kWh/m3, depending on the k’ value. The energy consumption decreased with higher the k’ value, except for increasing CD. The Boron Doped Diamond (BDD) was more effective in the decolorization rate than dimensional active anode (DSA) by 1.6 times. Treatment of industrial dye wastewater by the UV/EO process eliminated color intensity (ADMI), COD, and BOD5 by 80 %, 91 %, and 9 %, respectively.

Enhanced biomass densification pretreatment using binary chemicals for efficient lignocellulosic valorization

Many effective pretreatment methods (such as dilute acid, dilute alkali, ionic liquids, etc.) have been developed for lignocellulose upgrading, but several defaults of low working mass, high sugar loss and extra cost of solid-liquid separation and water washing hinder their large-scale application in industry. Besides, the valorization of lignin-rich residue from pretreated biomass after hydrolysis or fermentation greatly contributes to the economy and sustainability of lignocellulosic biorefinery, which is usually underestimated. This study developed a densification pretreatment with binary chemicals (densifying lignocellulosic biomass with sulfuric acid (SA) and metal salt (MS) followed by autoclave treatment ((DLCA(SA-MS)), which was conducted under mild condition (121 °C) with a biomass working mass as high as 400 kg/m3. The DLCA(SA-MS) biomass achieved over 95% sugar retention, 90% enzymatic sugar conversion and a high concentration of fermentable sugar (212.3 g/L) with superior fermentability. Furthermore, bio-adsorbent derived from DLCA(SA-MS) biomass residue was highly adsorptive and suitable for dyeing wastewater treatment, providing a feasible and eco-friendly method for lignin-rich residue valorization. These findings indicated that DLCA(SA-MS) pretreatment enables the full-component utilization of biomass and boosts the economic viability of lignocellulosic biorefinery.

Research Progress of Printing and Dyeing Wastewater Treatment

In the textile industry, printing and dyeing technology, as an essential technical basis, produces a lot of printing and dyeing wastewater (PDW) that jeopardizes the ecological environment and human health. PDW generally has the characteristics of large discharge, high chromaticity, strong toxicity, strong alkalinity, complex componentization, poor biodegradability, large fluctuations in water quality and quality, and high content of organic pollutants, belonging to the type of industrial wastewater that is difficult to manage. In this paper, the current research progress of PDW treatment technology from the aspects of physical technology, chemical technology, and biological technology are reviewed. In addition, measures to reduce the damage caused by printing and dyeing wastewater from three perspectives: treatment principle, processes, advantages, and disadvantages are discussed, which provides a reference point for the treatment of printing and dyeing wastewater. It is worth noting that the article reviews the ABS system, which is gaining attention as an emerging technology under biological technology. The purpose of this paper is to provide a reference basis for the selection and application of technology, and then promote the innovation and development of printing and dyeing wastewater treatment technology.

Bionic solar-Driven interfacial evaporator for synergistic photothermal-Photocatalytic activities and salt collection during desalination

Solar-driven interfacial evaporation plays an essential part in the production of potable water. Nevertheless, the intricate water conditions in real-world scenarios continue to pose limitations on its utilization. This study prepared a novel bionic PPy/BiVO4-PI/MXene aerogel composite material with radial center structure through directional freezing as the evaporator, which integrates both photothermal and photocatalytic properties into the evaporation system. In order to evaluate the efficacy of photocatalytic degradation and salt collection during interfacial evaporation, high-concentration saline water, simulated seawater and dyeing wastewater were employed as substitutes for real contaminated water bodies. After being exposed to 1 kW/m−2(−|-) of irradiation, the PPy/BiVO4-PI/MXene composite exhibits an evaporation rate of 1.64 kg m-2h−1 and achieves a photothermal efficiency of 96.77 %. In high-concentration saltwater containing 20 wt% NaCl, the PPy/BiVO4-PI/MXene exhibited an evaporation rate of 1.32 kg m-2h−1 and a photothermal conversion efficiency of 77.41 %. Furthermore, approximately 26.7 g of salt can be collected after 15 days’ continuous evaporation. Furthermore, the PPy/BiVO4-PI/MXene demonstrated exceptional photocatalytic capabilities to organic dyes such as MB, RhB, CR and MG with removal efficiencies of 79.28 %, 70.96 %, 76.70 % and 80.95 %, respectively. This study realizes the synergistic effect of interfacial evaporation, photocatalysis and salt collection, providing a highly promising choice for the treatment of high-salt dyeing wastewaters.

Hydrophilic and antimicrobial properties of hydroxypropyl trimethyl ammonium chloride chitosan/graphene oxide membrane for dye rejection

Graphene oxide (GO) -based membranes have attracted attention in dye wastewater treatment in recent years. However, water permeance and methyl orange (MO) rejection need improvement. In this work, a simple method was used to incorporate hydroxypropyl trimethyl ammonium chloride chitosan (HTCC) to enhance the charge of the membrane. An optimized HTCC-GO composite membrane (HGM membrane) containing a 2: 1 ratio of HTCC to GO membrane significantly improved MO rejection (96.94 %), and achieved high rejection of the other three dye molecules studied in this work (>93 %), and also realized a two-fold higher water permeance (28.09 L m−2 h−1 bar−1) compared to a pure GO membrane. Furthermore, the hydrophilic and antimicrobial properties of HGM membranes are enhanced as a result of quaternary ammonium groups in HTCC. Moreover, the acid-base stability of HGM membranes was also improved in comparison to the original GO membrane. This work provides a reference for the modification of GO-based membranes and their application in the direction of practical treatment of dye wastewater.

Occurrence and Ecological Risk Assessment of Highly Toxic Halogenated Byproducts during Chlorination Decolorization of Textile Printing and Dyeing Wastewater.

Textile printing and dyeing wastewater is a substantial source of highly toxic halogenated pollutants because of the chlorination decolorization. However, information on the occurrence and fate of the highly toxic halogenated byproducts, which are produced by chlorination decolorization of the textile printing and dyeing wastewater, is very limited. In this study, the occurrence of six categories of halogenated byproducts (haloacetic acids (HAAs), haloacetonitriles (HANs), N-nitrosamines (NAs), trihalomethanes, halogenated ketones, and halonitromethanes) was investigated along the full-scale treatment processes of textile printing and dyeing wastewater treatment plants. Furthermore, the ecological risk of the halogenated byproducts was evaluated. The results showed that the total concentration of halogenated byproducts increased significantly after chlorination. Large amounts of HAAs (average 122.1 μg/L), HANs (average 80.9 μg/L), THMs (average 48.3 μg/L), and NAs (average 2314.3 ng/L) were found in the chlorinated textile wastewater, and the results showed that the generations of HANs and NAs were positively correlated with the BIX and β/α index, indicating that the HANs and NAs might form from the microbial metabolites. In addition, HAAs and HANs exhibited high ecological risk quotients (>1), suggesting their high potential ecological risk. The results also demonstrated that most halogenated byproducts could be effectively removed by reverse osmosis treatment processes except NAs, with a lower removal rate of 18%. This study is believed to provide an important theoretical basis for controlling and reducing the ecological risks of halogenated byproducts in textile printing and dyeing wastewater effluents.

Application of chitosan/acid-treated biomass composite for dye wastewater treatment: Adsorption modeling using Box-Behnken Design

The use of chitosan polymer and acid-treated biomass composite as an eco-friendly and cost-effective solution for the removal of synthetic dyes from wastewater is a promising approach for sustainable wastewater treatment. The objective of the present investigation was to create a biocomposite (subsequently referred to as CHI/SFH-SA) by functionalizing chitosan (CHI) biopolymer with acid-treated biomass (sunflower husks-sulphuric acid (H2SO4), SFH-SA). Methods such as pHpzc, XRD, CHNS-O, FTIR, BET, and FESEM were employed to investigate the physicochemical properties of CHI/SFH-SA. The CHI/SFH-SA biocomposite's ability to eliminate brilliant green (BG) dye from aquatic systems was evaluated. To optimize the adsorption efficacy of CHI/SFH-SA, the Box-Behnken Design (BBD) was implemented. The design took into account parameters such as A: CHI/SFH-SA dose (0.02–0.08 g), B: pH (4–10), and C: time (10–60 min). The BBD model results showed that an optimal pH of 9.2, a contact duration of 59.1 min, and a CHI/SFH-SA dosage of 0.061 g were found to be the most effective conditions for achieving maximal BG dye elimination (95.89 %). The Langmuir and Freundlich models agree with the experimental data on BG dye adsorption by CHI/SFH-SA. Negative ΔG° values (−10.67, −12.09, −13.51, −14.93 kJ/mol) indicate spontaneous adsorption. Endothermic adsorption can be estimated with a positive ∆H° value of 31.65 kJ/mol. The adsorption capacity of CHI/SFH-SA was 485.56 mg/g. H-bonding, n-π interactions, and electrostatic forces are the primary factors responsible for the significant adsorption of BG dye onto CHI/SFH-SA. This research offers an environmentally conscious and sustainable approach to fabricating effective adsorbents, thereby establishing a foundation for developing bioadsorbents derived entirely from bioresources (chitosan and biomass), which hold great promise as a substitute for cationic dye removal.

Fabrication of temperature-regulated sorbitol/mannitol-doped copper oxides derived from a Cu complex and their photocatalytic properties

In this study, a series of composites containing copper oxide (CuxO) particles doped with sorbitol/mannitol, namely Cu/CuxO@C (x = 1 or 2), was successfully derived from a novel copper complex ([Cu(IPZ)2Cl2] (Cu-Complex), where IPZ = 4-Iodopyrazole) by pyrolysis method and exploiting the stability and modulation of the coordination sites of sorbitol/mannitol, which exhibited excellent photocatalytic properties. The results showed that Cu/CuxO@C possessed high efficiency in degrading rhodamine B (RhB), gentian violet (GV), methyl orange (MO) and Congo red (CR) dyes under UV irradiation, and the degradation effect was gradually enhanced with the increase of calcination temperature. The structural and chemical states of the materials were characterised in detail. Furthermore, the effects of experimental factors such as catalyst dose, solution pH, and inorganic anions on dye degradation efficiency were investigated. The photocatalytic mechanism study demonstrated that the primary oxygen-active substance was superoxide radical (·O2-). The electron transport hypothesis explains the effective separation of electrons and holes within a substance. The Cu/CuxO@C composite was regarded as a potential photocatalyst for dye wastewater treatment due to its high photocatalytic efficiency, reusability, and universality, offering a novel solution to environmental and energy issues.

Performance of Bioenergy Production from Durian Shell Wastes Coupled with Dye Wastewater Treatment

Adsorption using biochar is a high-efficient method for removing dyes from wastewater, and it has become a hot research topic in recent years. Biochar produced from organic wastes through pyrolysis is a promising way to combine bioenergy recovery and dye removal. In this study, durian shell (DS) was used as a feedstock for biochar and bio-oil production under different pyrolysis temperatures (400, 500, and 600 °C) for bioenergy recovery. Then, the biochar was applied as the absorbent for methylene blue (MB) removal from wastewater under batch and continuous experiments. It was found that the bio-oil production was slightly affected by temperature, while the productivity of biochar decreased from 42.05% to 30.65% with the increase in pyrolysis temperature from 400 to 600 °C. Compared with the biochar produced at 500 °C (DS-500) and 600 °C (DS-600), the biochar obtained at 400 °C (DS-400) exhibited higher MB removal efficiency and adsorption capacity under various pH conditions due to the superior microstructure. A high pH condition was beneficial for the adsorption process with DS-400. Additionally, the MB removal efficiencies increased with the increase in biochar dosage by providing more activated sites. A high MB content can promote the adsorption process, but a too high MB content negatively affects the removal efficiency due to the sorption saturation. Adsorption processes are more likely to match a pseudo-second-order model by chemical reactions. In the long-term continuous experiment, MB can be effectively removed to match the discharge standard by DS-400. This study provided a sustainable pathway for organic waste disposal and dye wastewater treatment.

Decolorization of industrial dye wastewater using an underwater non-thermal plasma system

The textile dyeing industry, in its developmental phase, significantly contributes to the discharge of large quantities of organic chemicals into rivers and oceans. Existing water purification technologies have not been effective in mitigating the associated risks. This study presents the development of a novel dielectric barrier discharge (DBD) plasma system aimed at decolorizing industrial dye wastewater through the generation of reactive oxygen species, ultraviolet light, ozone, and hydrogen peroxide. A new electrode configuration has been devised, exhibiting a 1.3-fold increase in energy consumption efficiency compared to conventional DBD plasma systems, facilitated by simultaneous cooling and discharging mechanisms. The proposed system showcases an 80 % reduction in chromaticity and achieves impressive removal performances, with 97 J/L within 1 min for methylene blue and 5527 J/L within 30 min for the treatment of industrial dye wastewater. This innovative DBD system promises to advance industrial wastewater treatment methodologies, potentially safeguarding aquatic ecosystems.

Efficient removal of cationic dyes by a bivanadyl capped, highly reduced Keggin polyoxometalate through flocculation

Flocculation is widely applied for dye wastewater treatment, due to its low cost, high efficiency and convenient operation. However, finding novel flocculant with high performance and low cost is still a challenge. Therefore, a fully characterized bivanadyl capped, highly reduced Keggin polyoxometalate (Et3NH)5[PMoV6MoVI6O40(VIVO)2] (PMoV2) was explored as flocculant for the treatment of simulated cationic dye wastewater. The effect of initial pH, PMoV2 dosage, and concentrations of dyes and inorganic salts on the flocculation rate of methylene blue (MB)/ crystal violet (CV)/rhodamine B (RhB) was investigated. Under the optimum conditions, the flocculation rates of MB, CV and RhB were 99.7 %, 99.8 % and 99.7 % in 5 min, respectively. In addition, PMoV2 and dyes could be easily recovered from flocs. PMoV2 exhibited high selectivity for CV in the binary systems of CV-MB and CV-MO. Even after five recycling tests, PMoV2 still kept high flocculation rate of MB/CV/RhB. The possible flocculation mechanisms for MB/CV/RhB single system, and MB-CV and MO-CV binary systems were charge neutralization, charge neutralization and π-π interaction, and charge neutralization and electrostatic interaction, respectively. PMoV2 was better than the reported flocculants in the respect of easy availability and operation conditions, reusability and high flocculation rate. The cost effectiveness, eco-friendly nature and excellent flocculation performance in individual and binary dye systems made PMoV2 competitive in the field of water environment remediation and material development. This is the first report about the flocculation activities of bivanadyl capped, highly reduced Keggin polyoxometalate.