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Textile, printing, and dyeing industries in China are expanding annually, resulting in the discharge of significant volumes of wastewater. These effluents have complex compositions and contain diverse pollutants that pose severe hazards to aquatic systems, ecological environments, and nearby flora, fauna, and human populations. The inadequate or rudimentary treatment of these effluents can cause substantial environmental damage. Current technologies for treating textile dyeing wastewater (TDW) include physical, chemical, and biological methods, with biological treatment being noted for its low cost and environmental sustainability. In the realm of biotechnological treatment, microorganisms, such as bacteria, fungi, and algae, exhibit significant potential. This review highlights the urgent need for effective treatment of textile dyeing wastewater (TDW), which poses severe environmental and health risks. It provides a comparative analysis of physical, chemical, and biological treatment methods, with a focus on the unique advantages of biological approaches, such as biodegradation and biosorption, for sustainable wastewater management. Key findings include recent advancements in microbial applications, challenges in scaling up, and integration into existing treatment systems. This review aims to guide future research and practical applications in achieving eco-friendly and cost-effective solutions for TDW remediation. [ABSTRACT FROM AUTHOR]

The degradation characteristics of aniline and antimony in printing and dyeing wastewater during the micro-oxygenated hydrolytic acidification process and its effect on COD and ammonia nitrogen removal were investigated in this experiment. Firstly, the effects of control factors such as pH, dissolved oxygen (DO), and sludge concentration on COD and ammonia nitrogen removal in the hydrolysis acidification section were optimized. It was recommended that the pH value should be maintained at 6.5; low DO (0–0.5 mg/L) could assist in the conversion of nitrogen for subsequent treatment; the optimum treatment temperature was 25 °C; finally, it was recommended that the sludge concentration should be controlled at 4 mg/L during the operation. Secondly, the effects of aniline and antimony on COD and nitrogen removal were investigated. It was found that when the concentration of aniline was increased from 0.4 mg/L to 5.4 mg/L, the COD concentration in the effluent increased by 96.5%, which indicated that aniline was toxic to anaerobic sludge and obviously inhibited the degradation of COD. When the concentration of antimony was increased from 0.05 mg/L to 2.05 mg/L, the COD removal rate was only 2.9%, which was much lower than that of the water samples with no antimony added. The anaerobic sludge concentration decreased from 5.58 g/L to 3.44 g/L, which indicated that aniline and antimony had a strong inhibitory effect on the activity of anaerobic bacteria and inversely affected COD removal. [ABSTRACT FROM AUTHOR]

In this study, novel Zn catalysts were prepared by the wet impregnation method using printing and dyeing wastewater (PDW)-modified petroleum coke (petcoke) as a carrier, and they were applied to the acetylene acetoxylation. The pretreated petroleum coke has a high specific surface area which provides sufficient space for the loading of Zn. Calcination further increases catalyst activity, but when calcination temperatures exceed 1000 °C, a significant loss of Zn occurs, resulting in a dramatic decrease in catalyst activity. This enables the conversion of acetic acid up to 85%. X-ray photoelectron spectroscopy confirmed that a large amount of N is introduced into PC from PDW, which changes the electron transfer around Zn. Temperature-programmed desorption (TPD) analysis revealed that the nitrogen-doped Zn(OAc)2 catalyst enhanced the catalytic activity by modulating the intensity of the catalyzed adsorption of acetic acid and acetylene. This study provides a new way to reuse petroleum coke and printing and dyeing wastewater to support the sustainable development of the vinyl acetate industry. [ABSTRACT FROM AUTHOR]

In recent years, electrochemical synergistic activation of persulfate (PDS) degradation technology has demonstrated significant potential in wastewater treatment applications. Given the challenges posed by the complex water quality, high COD content, and recalcitrant degradation of dyeing wastewater, this study aimed to evaluate the efficacy of iron/aluminum dual-electrode electrochemical activation of PDS for degrading simulated dyeing wastewater. The results showed that under optimal conditions, utilizing both periodic reversal and direct current electrochemical activation of PDS achieved removal rates of 99.2% and 98.3% for Reactive Black 5 (RB5) and Reactive Red X-3B (RRX-3B), respectively, demonstrating promising removal efficiency. Notably, the removal efficiency of RB5 surpassed that of RRX-3B, suggesting a dependence on initial concentration influencing reaction kinetics. Furthermore, full-spectrum scanning and quenching experiments revealed that RB5 and RRX-3B were primarily degraded through the potent oxidation action of SO4−· and ·OH, with a small number of intermediates present in the solution. Periodic reversal proved effective in mitigating electrode passivation and enhancing electrode longevity. This study provides a highly effective removal method of binary dyes from dyeing wastewater by periodic reversal Fe-Al dual-electrode electrochemical activation of PDS technology, offering valuable insights for sustainable treatment of dyeing wastewater with binary components. [ABSTRACT FROM AUTHOR]

The discharge of printing and dyeing wastewater has been increasing, causing serious environmental pollution with the rapid development of the industry. Based on this, an N self-doped mesoporous lotus leaf biochar (LLC800) was prepared from lotus leaves as raw material for the activation of Persulfate (PS) to degrade wastewater from printing and dyeing. The removal rate of AO7 by PS, LLC800 and LLC800/PS systems were 0.84%, 31.11% and 99.46%, respectively. Electron paramagnetic resonance spectroscopy (EPR) and quench tests showed the presence of free radicals (•OH, SO4●− and O2●−) and nonradical (1O2) in the LLC800/PS system, where nonradicals (1O2) play an important role in the degradation of AO7. The "N self-doped" effect formed by the high N content of lotus leaves is the main factor leading to the high adsorption and catalytic performance of lotus leaf biochar. The effect of pyrolysis temperature on the performance of biochar can be attributed to the change of N content and conformation and specific surface area in biochar. Moreover, the LLC800/PS system has a strong resistance to interference. This work can provide technical support for the preparation of high-performance adsorption-catalytic biochar and the development of high-performance activation materials for persulfate. [ABSTRACT FROM AUTHOR]

The organic dye malachite green (MG) poses a potential risk of cancer and fertility loss in humans and aquatic organisms. This study focused on a modified pyrolytic char (PC) derived from waste tires to efficiently remove MG from wastewater. Modified PC has rich -OH functional groups, higher BET (Brunauer-Emmett-Teller) surfaces of 74.4, 64.95, and 67.31 m2/g, and larger pore volumes of 0.52, 0.47, and 0.62 cm3/g for NaOH, Na2CO3, and CaO modification, respectively. The pseudo-second-order model fit the adsorption well, and the maximum equilibrium adsorption capacity was 937.8 mg/g for PC after CaO activation (CaO-PC). NaOH-modified PC (NaOH-PC) showed the best fit with the Langmuir model (R2 = 0.918). It is suggested that alkali-modified waste tire pyrolytic char could be a potential adsorbent for removing MG from dye-containing wastewater. [ABSTRACT FROM AUTHOR]

Nowadays, the structural complexity of dyes used in the textile industry and the widely adopted water-saving strategy in the dyeing processes often fail plants' biological wastewater treatment units due to chemical oxygen demand (COD) overload. To alleviate this problems, this study investigated a regenerable adsorption-oxidation process to treat dyeing wastewater with COD around 10,000 mg/dm 3 using a highly nano-pored activated carbon (AC) as a COD adsorbent, followed by its regeneration using hydrogen peroxide as an oxidizing reagent. In addition to studying AC's COD adsorption and oxidation performance, its operational treatment conditions in terms of temperature and pH were assessed. The results firstly demonstrated that about 50-60% of the COD was consistently adsorbed during the repeated adsorption operation before reaching AC's maximum adsorption capacity (q max ) of 0.165 g-COD/g-AC. The optimal pH and temperature during adsorption were 4.7 and 25 °C, respectively. Secondly, AC regeneration was accomplished by using an initial peroxide concentration of 2.5% (by wt %) and EDTA-Fe of 2.12 mmole/dm 3 . The reuse of the regenerated ACs was doable. Surprisingly, after the first AC regeneration, the COD adsorption capacity of the regenerated AC even increased by ~7% with respect to the virgin AC. Thirdly, the results of a five-consecutive adsorption-regeneration operation showed that a total of 0.3625 g COD was removed by the 5 g AC used, which was equivalent to an adsorption capacity (q) of 0.0725 (= 0.3625/5) g-COD/g-AC during each adsorption stage. Based on the obtained results, a regenerable COD adsorption-oxidation process using a nano-pored AC to treat the high-textile-COD wastewater looks promising. Thus, a conceptual treatment unit was proposed, and its potential benefits and limitations were addressed.

In this research, the preparation of a Ag 3 PO 4 /g-C 3 N 4 @MoS 2 photocatalyst and the performance and mechanism of degradation of 2-amino-4-acetaminoanisole (AMA) were studied. The phase composition and morphology of the synthesized samples were comprehensively characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), ultraviolet-visible diffuse reflectance (UV-Vis), and photoelectron spectroscopy (XPS). The catalytic performance of the photocatalyst was evaluated by the visible-light catalytic degradation of the AMA. The experimental results show that the Ag 3 PO 4 /g-C 3 N 4 @MoS 2 composite photocatalyst has stronger photocatalytic oxidation and reduction capabilities than Ag 3 PO 4 and Ag 3 PO 4 /g-C 3 N 4 . The material only decreases by 31.3% after five cycles of use, indicating that the material has good light stability. Free radical capture experiments prove that photo-generated holes (h + ) and superoxide radicals (·O 2 - ) are the main active substances in the photocatalytic process. The fundamental studies in the present research provide a new perspective for constructing an innovative type of visible-light photocatalyst and a new way to promote the photocatalytic degradation of organic pollutants.

This study investigates the influence of photoperiod and wastewater concentration on the growth of microalgae and cyanobacteria for the removal of environmentally significant parameters (COD, BOD, Cr, Fe, color, chlorides, nitrogen compounds, and phosphates) from dyeing wastewater. A two-factor central composite design with surface response was employed, involving two algae species (Chlorella and Scenedesmus sp.) and two cyanobacteria species (Hapalosiphon and Oscillatoria sp.). The findings indicated that extended photoperiods (>13 h) and higher wastewater concentrations (70–80% v/v) enhanced biomass production across all strains. However, Hapalosiphon and Chlorella sp. (1.6 and 0.45 g/L) exhibited better tolerance to the wastewater's high toxicity, resulting in higher biomass concentrations and improved COD and BOD removal by Hapalosiphon sp. (75% and 80%, respectively). Further analysis of the obtained biomass revealed their potential applications. Among the cyanobacteria, Hapalosiphon sp. synthesized the highest concentrations of total proteins and lipids (38% and 28% w/w, respectively), while Oscillatoria sp. displayed a high protein content (42% w/w). In contrast, the algae demonstrated a strong propensity for storing substantial quantities of total carbohydrates (65% and 57% w/w for Scenedesmus and Chlorella sp., respectively). These results signify the feasibility of cultivating photosynthetic microorganisms in industrial dyeing wastewater as a sustainable source of nutrients for targeted metabolite production. [ABSTRACT FROM AUTHOR]

Considering photocatalytic degradation technology has recently attracted great attention for dyeing wastewater treatment, the polyacrylonitrile (PAN) nanofibrous membrane coated with the TA/FeIII complexes was proposed as a novel photocatalyst in this work. The successful self-assembly of TA/FeIII complexes on the PAN nanofibrous membrane after layer-by-layer deposition of TA and FeIII was confirmed by the analyses of chemical structure, morphology, and hydrophilicity. With the number of coating cycles, more TA/FeIII complexes coated on the PAN nanofibrous membrane, which contributed to the excellent photocatalytic activity. Whereas, when the coating cycles reached seven, the photocatalytic performance of the modified PAN nanofibrous membrane deteriorated due to the serious aggregation of TA/FeIII complexes. Under optimum five coating cycles, owing to its great light absorbance capability, the modified PAN nanofibrous membrane achieved 98% degradation efficiency of RhB after 360 min illumination. This work would offer a promising high-performance photocatalyst for dyeing wastewater treatment. [ABSTRACT FROM AUTHOR]

To mitigate the potential environmental risks caused by nitrogen compounds from industrial wastewater, residual ammonia after conventional wastewater treatment should be further eliminated. In this work, an electrochemical oxidation process for converting ammonia to nitrogen in actual dyeing wastewater was investigated. The effects of the main operating parameters, including initial pH value, applied current density, NaCl concentration, and flow, were investigated on ammonia removal and products distribution. Experimental results indicated that, under optimal conditions of an initial pH value of 8.3, applied current density of 20 mA cm -2 , NaCl concentration of 1.0 g L -1 , and flow of 300 mL min -1 , the ammonia could be completely removed with N 2 selectivity of 88.3% in 60 min electrolysis. A kinetics investigation using a pseudo-first-order model provided a precise description of ammonia removal during the electro-oxidation process. Experimental functions for describing the relationships between kinetic constants of ammonia removal and main operating parameters were also discussed. Additionally, the mechanisms and economic evaluation of ammonia oxidation were conducted. All these results clearly proved that this electro-oxidation process could efficiently remove ammonia and achieve high N 2 selectivity.

Cost-effective treatment of dyeing wastewater remains a challenge. In this study, a newly designed hydrolysis acidification flat-sheet ceramic membrane bioreactor (HA-CMBR) was used in treating high-strength dyeing wastewater. The start-up phase of the HA-CMBR was accomplished in 29 days by using cultivated seed sludge. Chemical oxygen demand (COD) removal rate reached about 62% with influent COD of 7800 mg/L and an organic loading rate of 7.80 kg-COD/(m³·d). Chromaticity removal exceeded 99%. The results show that the HA-CMBR has good removal performance in treating dyeing wastewater. The HA-CMBR could run with low energy consumption at trans-membrane pressure (TMP) <10 kPa due to the good water permeability of the flat-sheet ceramic membrane. New strains with 92%⁻96% similarity to Alkalibaculum bacchi , Pseudomonas sp., Desulfovibrio sp., and Halothiobacillaceae were identified in the HA-CMBR. Microbial population analysis indicated that Desulfovibrio sp., Deltaproteobacteria , Halothiobacillaceae, Alkalibaculum sp., Pseudomonas sp., Desulfomicrobium sp., and Chlorobaculum sp. dominated in the HA-CMBR.

Herein, a preparation of a mixed-phase titanium dioxide (TiO2) thin layer on glass beads was developed using the modified spray method. This approach was determined to be affordable and easy to operate. Optimum conditions were investigated for the photodegradation of wastewater generated from textile dyeing by TiO2-coated glass beads as a catalyst using the central composite design (CCD). An increase in the direct dye photodegradation rate was observed at lower direct dye concentrations when TiO2 dosages were increased, and the initial pH value was decreased. The optimal conditions involving TiO2 dosage, pH, UV intensity, and dye concentrations were 3 g/L, 5.0, 3000 µW/cm2, and 50 mg/L, respectively, when administered at ambient temperatures. For the batch experiments, the direct dye removal efficiency at 93.7% was achieved within 24 h. The average direct dye removal efficiency was 67.8% and could be up to 80.2% when using a fixed-bed photocatalysis reactor during 30 d of continuous operation. The reused catalyst's degradation efficiency was not significantly changed, indicating its capability for repeated reuse and the excellent stability of immobilized TiO2 onto the glass beads. This study additionally found that high temperatures could increase the efficiency of color removal. [ABSTRACT FROM AUTHOR]

Technological advancement, on the one hand, leads to the enhanced quality of the final product but on the other hand, generates a good quantity of effluent. The wastewater containing dyes which emanates from the textile industry is a cause of worry. Hence, this paper focuses on the treatment of dyeing wastewater using the foam separation process as it offers several advantages over other traditional methods. Methylene blue (MB), owing to its ill effects on the entire ecosystem, has been considered as a model dye in this research work. The objective of this work is to remove MB from wastewater and at the same time, its recovery in the foam phase. The ability of sodium dodecyl sulfate (SDS) and sodium dodecyl benzene sulfonate (SDBS) to perform separation of MB was compared. The following operating parameters were identified: contact time, initial pH of a feed solution, surfactant dose, volumetric flow rate of air, volume of liquid in the column, and concentration of dye; which greatly influence the separation parameters (% removal and enrichment ratio). Keeping in mind the importance of recovering MB from dilute solutions, the method to enhance foam drainage was devised by inserting an inverted funnel in the foam phase. In the presence of inverted funnel, the concentration of MB in the foamate doubled in comparison to the conventional column (without an inverted funnel). The comparison between SDS and SDBS divulged SDBS as a better surfactant to get concentrated solution of MB in the foamate, but the quantity of SDBS required was more. The optimization of operating variables was also done by using the Taguchi method and Grey relational analysis. Finally, the concentration of MB was discovered to be the most responsive operating parameter for both separation parameters. [ABSTRACT FROM AUTHOR]

The textile industry is a global economic driving force; however, it is also one of the most polluting industries, with highly toxic effluents which are complex to treat due to the recalcitrant nature of some compounds present in these effluents. This research focuses on the removal of Chemical Oxygen Demand (COD), color, Total Organic Carbon (TOC), and Ammoniacal Nitrogen (N-NH3) on tannery wastewater treatment through an advanced oxidation process (AOPs) using sodium bicarbonate (NaHCO3), hydrogen peroxide (H2O2) and temperature using a central composite non-factorial design with a surface response using Statistica 7.0 software. All experiments used a 500 mL reactor with 300 mL of tannery wastewater from a company in Cúcuta, Colombia. The physicochemical characterization was done to determine the significant absorbance peaks about the color in the wavelengths between 297 and 669 nm. Statistical analysis found that the concentration of NaHCO3 affects the removal of color and N-NH3; however, it did not affect COD and TOC. The optimal process conditions for removing the different compounds under study were: NaHCO3 1 M, H2O2 2 M, and 60 °C, with efficiencies of 92.35%, 31.93%, 68.85%, and 35.5% N-NH3, COD, color, and TOC respectively. It can be concluded that AOPs using H2O2 and NaHCO3 are recommended to remove color and N-NH3. [ABSTRACT FROM AUTHOR]

Wastewater reuse has been addressed to promote the sustainable water utilization in textile industry. However, conventional technologies are unable to deliver treated wastewater with the quality required for reuse, mainly due to the presence of dyes and high salinity. In this work, the feasibility of electrooxidation, using a boron-doped diamond anode, to provide treated textile dyeing wastewater (TDW) with the quality required for reuse, and with complete recovery of salts, was evaluated. The influence of the applied current density on the quality of treated TDW and on the consecutive reuse in new dyeing baths was studied. The ecotoxicological evaluation of the process towards Daphnia magna was performed. After 10 h of electrooxidation at 60 and 100 mA cm−2, discolorized treated TDW, with chemical oxygen demand below 200 (moderate-quality) and 50 mg L−1 (high-quality), respectively, was obtained. Salt content was unchanged in both treatment conditions, enabling the consecutive reuse without any salt addition. For the two reuse cycles performed, both treated samples led to dyed fabrics in compliance with the most restrictive controls, showing that an effective consecutive reuse can be achieved with a moderate-quality water. Besides the water reuse and complete salts saving, electrooxidation accomplished an ecotoxicity reduction up to 18.6-fold, allowing TDW reuse without severe ecotoxicity accumulation. [ABSTRACT FROM AUTHOR]

A pilot-scale six-compartment hybrid anaerobic baffled reactor (HABR) with effective volume of 18 m3 was used to treat dyeing wastewater. The HABR system was able to treat the wastewater efficiently after FeSO4 pretreatment, as indicated by removal efficiencies of 33.7% for chemical oxygen demand (COD), 39.9% for suspended solid (SS), and 22.5% for sulfate (SO42−) during steadily operational period. Gas chromatography–mass spectrometry (GC-MS) showed that the concentrations of alkanes, amides, organic acids, ketones, phenols, and esters were much lower in the effluent than those in the influent; many high-molecular-weight compounds such as cyclanes, quinolines, and phenols were successfully transformed to low-molecular-weight ones. As illustrated from the results of generalized grey relational analysis (GGRA), COD removal efficiency was more closely associated with flow rate, organic loading rate (OLR), water temperature, and influent SS among the whole selected possible factors. Based on the overall treating effectiveness and the GGRA study, the optimized operation strategy of the dyeing wastewater treatment by HABR was obtained as the hydraulic retention time (HRT) of 12 h for steady-state operation with an up-flow velocity of 1.7 m/h as well as OLR of 1.5–2.0 kg COD/(m3·d). [ABSTRACT FROM AUTHOR]

TiO2 is widely used for the photocatalytic degradation of organic pollutants in wastewater, but the practical applications of the photocatalyst are limited due to its poor visible light absorption and low recovery rate. In this study, high production of nitrogen-doped TiO2 was achieved by a hydrolysis precipitation method; the obtained N-TiO2 had a small crystallite size and good dispersibility. The effect of calcining temperature on the photocatalytic performance of N-TiO2 was evaluated through the degradation of methylene blue (MB) in a blue light LED irradiation cylinder, it was found the N-TiO2 calcined at 400 °C showed the best photocatalytic activity. Then the N-TiO2 was immobilized on SiC ceramic foam by dip-coating with PVA as the binder. The prepared N-TiO2/SiC foam showed excellent photocatalytic activity under blue light LED irradiation; as high as 96.3% of MB was degraded at optimum conditions. After five cycles of MB photodegradation, the photocatalytic activity of N-TiO2/SiC foam only changed slightly, which makes it a promising photocatalytic material for wastewater treatment. [ABSTRACT FROM AUTHOR]

Due to the severe harmful impacts of industrial dyeing wastewater on ecosystems and human health, proper treatment is crucial. Herein, the use of modified graphite as an adsorbent for dyeing wastewater treatment was investigated in this study. The graphite was oxidized and intercalated using a phosphoric acid–nitric acid–potassium permanganate system and then thermally treated at high temperatures to optimize its structure. By adjusting the thermal treatment temperature, the graphite adsorbent with varying porosity was obtained. The optimized graphite demonstrated significant improvement in adsorption performance for dyes and organic compounds, achieving a removal rate of over 85% for methylene blue (MB) dye. The optimal adsorption performance is achieved with a 1.6 mg modified graphite adsorbent at 60 °C under alkaline conditions for adsorbing 10 ppm MB. Adsorption kinetics and isotherm models were applied to elucidate the adsorption mechanisms. The results fit the Langmuir model, suggesting that monolayer homogeneous adsorption is favorable. Importantly, the results demonstrate that high-temperature treatment can significantly enhance the adsorption properties of coal-based graphite, supporting its application in dyeing wastewater treatment. [ABSTRACT FROM AUTHOR]

Polymerized aluminum magnesium chloride (PAMC) flocculant was prepared from gangue as a raw material, and the effects of pH, the polymerization time, and the polymerization temperature on the performance of the PAMC were investigated by a one-factor test, based on which, orthogonal experiments (three-factor and two-level) were conducted to optimize the relevant parameters. Meanwhile, FTIR and SEM were used to characterize the polymerized aluminum magnesium chloride, and the sample was applied in printing and dyeing wastewater treatment. The results showed that a pH value of 2.2 and a reaction at 60 °C for 4.5 h were the optimal preparation conditions; the characterization analysis showed that the synthesized product was polymerized aluminum magnesium chloride; the turbidity removal rate of the PAMC for printing and dyeing wastewater was increased by 2.1%, the COD removal rate was increased by 3.1%, the ammonia nitrogen removal rate was increased by 2.1%, and the chromaticity removal rate was increased by 9.2% compared with that of PAC. [ABSTRACT FROM AUTHOR]

Simple Summary: The accumulation of recalcitrant pollutants (e.g., lignin biomass and synthetic textile dyes) in diverse ecosystems has exacerbated the problem of environmental pollution. The complex polymer structure of lignin brings huge challenges to the development of high-efficiency transformation technology, making it difficult to realize its industrial utilization. On the other hand, the use of dyes in the textile industry poses significant challenges worldwide. Dyes are very similar to lignin biomass in chemical structure. Similarly, under natural conditions, it is difficult for microorganisms in the environment to achieve rapid biodegradation and complete detoxification. Clearly, the integration of bioremediation and biorefinery technology towards such recalcitrant organic wastes is considered a novel concept for mitigating the toxicity of such pollutants using termite gut symbionts. Modern biorefinery and bioremediation applications can integrate the termite gut system, a unique bioresource that comprises distinct bacterial species valued for lignocellulosic material processing and synthetic dye degradation. Therefore, this review paper provides a new strategy for efficient management of recalcitrant pollutants by exploring the potential application of termite gut bacteria in terms of science and industry. Lignocellulosic biomass (LCB) in the form of agricultural, forestry, and agro-industrial wastes is globally generated in large volumes every year. The chemical components of LCB render them a substrate valuable for biofuel production. It is hard to dissolve LCB resources for biofuel production because the lignin, cellulose, and hemicellulose parts stick together rigidly. This makes the structure complex, hierarchical, and resistant. Owing to these restrictions, the junk production of LCB waste has recently become a significant worldwide environmental problem resulting from inefficient disposal techniques and increased persistence. In addition, burning LCB waste, such as paddy straws, is a widespread practice that causes considerable air pollution and endangers the environment and human existence. Besides environmental pollution from LCB waste, increasing industrialization has resulted in the production of billions of tons of dyeing wastewater from several industries, including textiles, pharmaceuticals, tanneries, and food processing units. The massive use of synthetic dyes in various industries can be detrimental to the environment due to the recalcitrant aromatic structure of synthetic dyes, similar to the polymeric phenol lignin in LCB structure, and their persistent color. Synthetic dyes have been described as possessing carcinogenic and toxic properties that could be harmful to public health. Environmental pollution emanating from LCB wastes and dyeing wastewater is of great concern and should be carefully handled to mitigate its catastrophic effects. An effective strategy to curtail these problems is to learn from analogous systems in nature, such as termites, where woody lignocellulose is digested by wood-feeding termites and humus-recalcitrant aromatic compounds are decomposed by soil-feeding termites. The termite gut system acts as a unique bioresource consisting of distinct bacterial species valued for the processing of lignocellulosic materials and the degradation of synthetic dyes, which can be integrated into modern biorefineries for processing LCB waste and bioremediation applications for the treatment of dyeing wastewaters to help resolve environmental issues arising from LCB waste and dyeing wastewaters. This review paper provides a new strategy for efficient management of recalcitrant pollutants by exploring the potential application of termite gut bacteria in biorefinery and bioremediation processing. [ABSTRACT FROM AUTHOR]

The dilemma of diminishing freshwater resources caused by water pollution has always impacted human life. Solar-driven interfacial evaporation technology has the potential for freshwater production via solar-driven distillation. However, in solar-driven interfacial evaporation technology, it is difficult to overcome the problem of wastewater containing various contaminants. In this work, we propose a bifunctional fabric created by depositing titanium dioxide@carbon black nanoparticles onto cotton fabric (TiO2@CB/CF). The TiO2@CB/CF has a coupling effect that includes the photothermal effect of CB and photocatalysis of TiO2, and it can not only generate clean water but can also purify contaminated water. The resulting bifunctional fabric can achieve an outstanding water evaporation rate of 1.42 kg m−2 h−1 and a conversion efficiency of 90.4% in methylene blue (MB) solution under one-sun irradiation. Simultaneously, the TiO2@CB/CF demonstrates a high photocatalytic degradation of 57% for MB solution after 2 h with light irradiation. It still shows a good photocatalysis effect, even when reused in an MB solution for eight cycles. Furthermore, the TiO2@CB/CF delivers excellent performance for actual industrial textile dyeing wastewater. This bifunctional fabric has a good application prospect and will provide a novel way to resolve the issue of freshwater scarcity. [ABSTRACT FROM AUTHOR]

Vast amounts of dyeing wastewater released from the textile industry can not only cause water pollution but also have negative effects on the human body, such as skin irritation and respiratory diseases. Dye adsorption technology is necessary for the treatment of wastewater discharged from the dyeing industry and for environmental improvement. However, to remove dyeing wastewater, more energy and solvents are used to fabricate adsorbents, or excessive energy is used to filter dyeing wastewater out, resulting in more environmental pollution. Therefore, it is necessary to develop a method of filtering dyeing wastewater in a more environmentally friendly manner by minimizing the use of solvents and energy. In this study, we modified the surface of a textile substrate through UV irradiation to create a monomer capable of facilely bonding with dyes. Employing the UV photografting method, we were able to produce a dye adsorption filter in a more environmentally friendly manner, minimizing solvent usage and heat energy consumption required for absorbent synthesis. At a monomer concentration of 10%, the fabricated filter exhibited a dye removal efficiency of 97.34% after 24 h, all without the need for a pressure treatment or temperature increase. Moreover, it displayed an adsorption capacity of approximately 77.88 mg per 1 g of filter material. [ABSTRACT FROM AUTHOR]

Microplastic pollution has become a global environmental problem. Textile microplastics are an important component of microplastic pollution, but little is known about their contamination in the industrial environment. The lack of standardized methods for detecting and quantifying textile microplastics is a major obstacle to determining the risks they pose to the natural environment. This study systematically examines the pretreatment options for the extraction of microplastics from printing and dyeing wastewater. The effectiveness of potassium hydroxide, nitric acid–hydrogen peroxide mixed solution, hydrogen peroxide, and Fenton's reagent for the removal of organic matter from textile wastewater is compared. Three textile microplastics, polyethylene terephthalate, polyamide, and polyurethane, are studied. The effects of the digestion treatment on the physicochemical properties of textile microplastics are characterized. The separation efficiency of sodium chloride, zinc chloride, sodium bromide, sodium iodide, and sodium chloride-sodium iodide mixed solution on the textile microplastics is tested. The results showed that Fenton's reagent achieved a 78% removal rate of organic matter from printing and dyeing wastewater. Meanwhile, it has less of an effect on the physicochemical properties of textile microplastics after digestion and is the best reagent for digestion. The zinc chloride solution achieved a 90% recovery for separating textile microplastics with good reproducibility. It does not affect the subsequent characterization analysis after separation and is the best solution for density separation. [ABSTRACT FROM AUTHOR]

At present, the use of conventional reactive dyes on banana-fiber fabric leads to the problem of excessive salt consumption, which is not conducive to environmental protection. In this experimental study, rare-earth-pretreated banana-fiber fabric was dyed with the reactive dye Argazol Navy Blue. The rare-earth pretreatment was carried out to reduce the level of salt consumption, improve dyeing and fixation rates, and reduce the treatment burden of printing and dyeing wastewater. Dye uptake and fixation rates were used as indicators. Single-change factors were assessed by analyzing different amounts of rare earth, sodium carbonate, and sodium chloride, as well as different fixation times and temperatures, so that the effects of the dye additive on the dyed banana-fiber fabric could be investigated. After appropriate ranges were determined for single-change factors, an orthogonal experiment was carried out to establish optimal parameters for the process of dyeing rare-earth-pretreated banana-fiber fabric with Argazol Navy Blue. These parameters were as follows: the required amount of rare earth was 0.40% (o.w.f.); the amount of dye was 2% (o.w.f.); the amount of sodium chloride was 15 g/L; the amount of sodium carbonate was 9 g/L; the fixing temperature was 75 °C; and the fixing time was 45 min. These optimized process parameters were then used to dye the banana-fiber fabric as a whole. Our results showed that the dye uptake and fixation rates for rare-earth-pretreated banana-fiber fabric dyed with navy-blue dye reached 56.85% and 45.32%, respectively. Finally, the effect of rare-earth pretreatment on dyeing performance was analyzed using FT-IR, SEM, and EDS. [ABSTRACT FROM AUTHOR]

Two porphyrin-based polymeric frameworks, SnP-BTC and SnP-BTB, as visible light photocatalysts for wastewater remediation were prepared by the solvothermal reaction of trans-dihydroxo-[5,15,10,20-tetrakis(phenyl)porphyrinato]tin(IV) (SnP) with 1,3,5-benzenetricarboxylic acid (H3BTC) and 1,3,5-tris(4-carboxyphenyl)benzene (H3BTB), respectively. The strong bond between the carboxylic acid group of H3BTC and H3BTB with the axial hydroxyl moiety of SnP leads to the formation of highly stable polymeric architectures. Incorporating the carboxylic acid group onto the surface of SnP changes the conformational frameworks as well as produces rigid structural transformation that includes permanent porosity, good thermodynamic stability, interesting morphology, and excellent photocatalytic degradation activity against AM dye and TC antibiotic under visible light irradiation. The photocatalytic degradation activities of AM dye were found to be 95% by SnP-BTB and 87% by SnP-BTC within 80 min. Within 60 min of visible light exposure, the photocatalytic degradation activities of TC antibiotic were found to be 70% by SnP-BTB and 60% by SnP-BTC. The enhanced catalytic photodegradation performances of SnP-BTB and SnP-BTC were attributed to the synergistic effect between SnP and carboxylic acid groups. The carboxylic acid connectors strongly resist the separation of SnP from the surface of SnP-BTB and SnP-BTC during the photodegradation experiments. Therefore, the high degradation rate and low catalyst loading make SnP-BTB or SnP-BTC more efficient than other reported catalysts. Thus, the present investigations on the porphyrin-based photocatalysts hold great promise in tackling the treatment of dyeing wastewater. [ABSTRACT FROM AUTHOR]

The disposal process of iron-containing sludge often leads to secondary pollution. Pyrolysis of sludge appears to be less polluting than conventional methods. Herein, the heterogeneous photo-Fenton catalysts were prepared using sludge generated in the dyeing wastewater through a simple one-step pyrolysis route. The catalysts were characterized by XRD, FT-IR, XPS, EDS, BET, and SEM. The batch experiments for methyl orange (MO) degradation were performed to evaluate the efficiency and stability of the catalysts. Among the catalysts prepared, FeCN-300 exhibited the best degradation efficiency with 92% removal of the pollutant and good stability, with approximately 90% removal of the pollutant after five cycles. The •OH was identified as the dominant reactive species. This work provides a reasonable resource utilization of iron-containing sludge. [ABSTRACT FROM AUTHOR]

According to the characteristics of aniline dyeing wastewater, aerobic biological treatment was adopted herein, and high-throughput sequencing technology was used to analyze the changes to the microbial community structure and diversity in the aerobic sludge acclimation stage. As a result, according to the experimental study on the effects of different biomass, the initial pH value and the salinity with the aerobic biological treatment, the chemical oxygen demand (COD) degradation rate can increase linearly with the increase in biomass under different biomass conditions. The organic matter degradation rate is 6.24 mg/L COD·h−1·(mg/L·MLSS)−1, with a correlation coefficient (R2) of 0.98704. When the initial pH value is less than 7.0 ± 0.2, the COD degradation rate increases with the increase in the initial pH value and then decreases gradually. The optimal sludge concentration is 4 g/L; the optimal initial pH value is in the range of 7.0–8.0; the optimal salinity is 1.7%. When the initial concentration of COD is 3000 mg/L, the COD value gradually stabilizes and decreases to 1500 mg/L after 32 h, the degradation rate reaches 50%, and the pH decreases from 7.5 to 4.5. Sphingopyxis has been detected in sludge samples from the third cycle of acclimation, which can biodegrade aromatic compounds, anthraquinone dyes, and their intermediates, and the relative abundance of Sphingopyxis increased from 0.18% to 5.08%, indicating a potential biodegradation ability of aniline dyeing wastewater. [ABSTRACT FROM AUTHOR]

This study investigated the symbiotic structure relationship between mixed algae and activated sludge while treating high-load printing and dyeing wastewater under natural light. The effects of hydraulic retention time (HRT) (12 h, 16 h and 20 h) and aeration rate (0.1–0.15, 0.4–0.5 and 0.7–0.8 L/min) on algal–bacterial symbiosis (ABS) and conventional activated sludge (CAS) systems. Experimental results showed that the ABS system exhibited the best removal performance for chemical oxygen demand (COD), ammonia nitrogen (NH4+-N) and total phosphorus (TP), which was increased by 12.5%, 23.1% and 10.5%, respectively, and reduced colour 80 times compared with the printing and dyeing wastewater treatment plant. Algae growth could be promoted under lower dissolved oxygen (DO), and the addition of algae could provide more DO to the ABS system. The particle size distribution of sludge in the ABS system was stable, which guaranteed a stable treatment effect. In addition, the COD and colour could be further degraded under the conditions of no external carbon source and longer HRT. It is expected that the present study will provide a foundation for the practical application of the ABS system, and new insights for the treatment of printing and dyeing wastewater. [ABSTRACT FROM AUTHOR]

A modified loess/chitosan composite (ML@CS) was prepared via solution. The microstructure and physicochemical properties of ML@CS were characterised via scanning electron microscope (SEM), Zeta potential, X-ray diffraction (XRD), Fourier transform infrared spectrum (FT-IR), and thermogravimetric analysis (TGA). An aqueous solution of methyl orange (MO) was used as simulated wastewater from which the influence of the initial concentration and pH of MO, the dosage amount and regeneration performance of ML@CS, adsorption temperature, and time on the adsorption effect of MO were systematically investigated. The adsorption kinetics, isothermal adsorption, and adsorption mechanism were also analysed. The results indicate that ML@CS had a good adsorption effect on MO. When the initial concentration of MO was 200 mg/L, pH was 5.0, and ML@CS dosage was 1.0 g/L, the adsorption equilibrium could be reached within 180 min at room temperature, and the equilibrium adsorption capacity and removal rate reached 199.52 mg/g and 99.75%, respectively. After five adsorption–desorption cycles, the MO removal rate remained above 82%. The adsorption behaviour of ML@CS for MO conforms to the pseudo–second–order kinetic model and the Langmuir isotherm adsorption model. The spontaneous exothermic process was mainly controlled by monolayer chemical adsorption and the physical adsorption only played an auxiliary role. ML@CS efficiently adsorbed MO in water and can be used as a high-efficiency, low-cost adsorbent for printing and dyeing wastewater treatment. [ABSTRACT FROM AUTHOR]

The in situ electrochemical oxidation process has received considerable attention for the removal of dye molecules and ammonium from textile dyeing and finishing wastewater. Nevertheless, the cost and durability of the catalytic anode have seriously limited industrial applications of this technique. In this work, the lab-based waste polyvinylidene fluoride membrane was employed to fabricate a novel lead dioxide/polyvinylidene fluoride/carbon cloth composite (PbO2/PVDF/CC) via integrated surface coating and electrodeposition processes. The influences of operating parameters (pH, Cl− concentration, current density, and initial concentration of pollutant) on the oxidation efficiency of PbO2/PVDF/CC were evaluated. Under optimal conditions, this composite achieves a 100% decolorization of methyl orange (MO), 99.48% removal of ammonium, and 94.46% conversion for ammonium-based nitrogen to N2, as well as an 82.55% removal of chemical oxygen demand (COD). At the coexistent condition of ammonium and MO, MO decolorization, ammonium, and COD removals still remain around 100%, 99.43%, and 77.33%, respectively. It can be assigned to the synergistic oxidation effect of hydroxyl radical and chloride species for MO and the chlorine oxidation action for ammonium. Based on the determination of various intermediates, MO is finally mineralized to CO2 and H2O, and ammonium is mainly converted to N2. The PbO2/PVDF/CC composite exhibits excellent stability and safety. [ABSTRACT FROM AUTHOR]

The pollution caused by printing and dyeing wastewater is increasingly severe, posing significant harm to aquatic plants and animals. In this study, porous carbon was synthesized via the high-temperature pyrolysis of light and heavy organic matter present in oily sludge, utilizing low oil content sludge as the raw material and zinc chloride as a chemical activator. The results exhibited a significant increase in the specific surface area of the oily sludge-based porous carbon, from 4.95 m²/g to 10.95 m²/g. The effects of various parameters such as pH, amount of sorbent, dye concentration, temperature, and contact time on dye removal have been studied. The results showed that the oil sludge-based porous carbon exhibited high efficiency in removing Malachite Green from aqueous solutions, which has low polarity and remains consistently above 97%. The removal rate of Crystal Violet, which is more polar, was as low as 24.14%. The corresponding adsorption capacities were 33.41 mg/g for Malachite Green, 16.41 mg/g for Crystal Violet, and 13.56 mg/g for Methylene Blue. The adsorption capacity of OSC700 for three types of dyes was characterized by monolayer adsorption, primarily driven by chemical adsorption, with significant contributions from electrostatic and hydrophobic effects. The adsorption process was spontaneous, exothermic, and accompanied by an increase in entropy. For less polar substances, the adsorption on oily sludge-based porous carbon is primarily driven by aromatic functional groups on the carbon surface, hydrophobicity, π-π electron-donor-acceptor (π-π EDA) interactions, and surface hydrogen bond formation. In contrast, for more polar dyes, electrostatic and hydrophobic interactions dominate, with electrostatic adsorption being the predominant mechanism and minimal hydrogen bond formation during adsorption. [ABSTRACT FROM AUTHOR]

The awareness of the concept of the "Circular Economy" is motivating scientists to convert drinking water treatment plant by-products, which are based on aluminum waste, into a valorized material for wastewater treatment. Alum sludge from a local waterworks plant in Egypt was collected and dewatered using chitosan-coated magnetic nanoparticles. The role of the conditioned sludge in wastewater treatment was then examined. Chitosan (Ch) augmented with magnetite nanoparticles (MNs), labeled as ChMNs, was prepared by means of a simple co-precipitation route with mixing ratios of 1:1, 2:1, and 3:1 of chitosan and magnetite nanoparticles to form the ChMN catalyst. The ChMNs were shown to beneficially enhance alum sludge conditioning and dewaterability. The conditioned and dried aluminum-based sludge (AS) loaded with ChMNs was then used as a source of Fenton's catalyst for Synozol Red-KHL textile dyeing wastewater. The characteristics of the AS-ChMN sample were investigated using Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). The photocatalytic activity of the AS-ChMN composite was assessed by examining its diffuse reflectance spectra (DRS). Response surface methodological analysis was applied to optimize the operational parameters in order to reduce the use of chemicals and improve dye oxidation to form a complete (99%) dye oxidation strategy. The experiments demonstrated that the optimal operating parameters included doses of 1.5 g/L and 420 mg/L for AS-ChMNs and hydrogen peroxide, respectively, as a source of Fenton's reaction at a working pH of 3.5. Kinetic and thermodynamic analyses for potential full-scale applications were conducted, showing the reaction to be exothermic and spontaneous in nature and following second-order reaction kinetics. Hence, the novelty of this work lies in the introduction of conditioned and dewatered alum sludge waste as a photocatalyst for textile dye effluent oxidation, which could be considered a "win–win" strategy. [ABSTRACT FROM AUTHOR]

Heterogeneous photo–Fenton reactions have been regarded as important technologies for the treatment of textile dyeing wastewaters. In this work, an efficient core-shell magnetic anion exchange resin (MAER) was prepared through in situ polymerization and used to remove reactive brilliant red (X-3B) in a UV–Fenton system. The MAER exhibited satisfactory removal efficiency for X-3B because of its highly effective catalytic activity. More than 99% of the X-3B (50 mg/L) was removed within 20 min in the UV–Fenton reaction. This is because the uniformly dispersed core-shell magnetic microsphere resin could suppress the aggregation of Fe3O4 nanoparticles and, thus, enhance the exposure of Fe reaction sites for catalytic reaction with H2O2. The good adsorption capacity of MAER also played an important role in promoting contact between X-3B and reactive radicals during the reaction. Mechanism research showed that hydroxyl radical (•OH) was the main reactive radicals for the removal of X-3B in the MAER UV–Fenton system. The MAER can be easily separated by a magnet after catalytic reactions. Moreover, the matrix effects of different substrates (Cl−, NO3−, SO42−, and humic acid) were investigated. The results showed that SO42− could be beneficial to improve the removal of X-3B but that the others decrease the removal. The MAER UV–Fenton also removed significant amounts of total organic carbon (TOC) for the X-3B solution and an actual textile dyeing industrial wastewater. The heterogeneous oxidation system established in this work may suggest prospects for practical applications in the treatment of textile dyeing wastewater. [ABSTRACT FROM AUTHOR]

In order to remove and reuse the ecotoxic dye Eriochrome black T (EBT) from dyeing wastewater, we used a process called cetyltrimethylammonium bromide (CTAB)-assisted foam fractionation. By optimizing this process with response surface methodology, we achieved an enrichment ratio of 110.3 ± 3.8 and a recovery rate of 99.1 ± 0.3%. Next, we prepared composite particles by adding β-cyclodextrin (β-CD) to the foamate obtained through foam fractionation. These particles had an average diameter of 80.9 μm, an irregular shape, and a specific surface area of 0.15 m2/g. Using these β-CD-CTAB-EBT particles, we were able to effectively remove trace amounts of Cu2+ ions (4 mg/L) from the wastewater. The adsorption of these ions followed pseudo-second-order kinetics and Langmuir isotherm models, and the maximal adsorption capacities at different temperatures were 141.4 mg/g at 298.15 K, 143.1 mg/g at 308.15 K, and 144.5 mg/g at 318.15 K. Thermodynamic analysis showed that the mechanism of Cu2+ removal via β-CD-CTAB-EBT was spontaneous and endothermic physisorption. Under the optimized conditions, we achieved a removal ratio of 95.3 ± 3.0% for Cu2+ ions, and the adsorption capacity remained at 78.3% after four reuse cycles. Overall, these results demonstrate the potential of β-CD-CTAB-EBT particles for the recovery and reuse of EBT in dyeing wastewater. [ABSTRACT FROM AUTHOR]

This study investigated if biochar, a low-cost carbon-rich material, can be modified with reactive materials for decolorization of dyeing wastewater. Two types of rice husk biochars were produced by using different processes of gasification and pyrolysis in limited air condition. The biochars were first magnetized and then modified with nano-scale zero-valent iron (nZVI) to achieve the final products of magnetic-nZVI biochars. Batch experiments were conducted to investigate the efficiency of the modified biochars for reducing color of the reactive dyes yellow (RY145), red (RR195), and blue (RB19) from dyeing solutions. Results showed that color removal efficiency of the modified biochars was significantly enhanced, achieving the values of 100% for RY145 and RR195 and ≥65% for RB19, while the effectiveness of the original biochar was significantly lower. In addition, with increasing dose of the modified biochars, the color removal efficiency increased accordingly. In contrast, when the dose of nZVI was increased beyond a certain value then its color removal efficiency decreased accordingly. It is reported that the magnetic-nZVI rice husk biochars effectively removed the reactive dyes. The impregnation of nZVI particles on the biochar surface spatially separates the nZVI particles, prevents its aggregation and therefore enhances the decolorization efficiency. [ABSTRACT FROM AUTHOR]

The dyes in printing and dyeing wastewater are harmful to the human body and the environment. It is essential to develop practical and effective adsorbents to deal with them. In this study, an Fe-doped, ZIF-67 derived Fe/Co/C composite material with strong magnetism was successfully synthesized. The effects of pH, initial concentration, and adsorption time on the properties of the adsorbent were investigated. To further improve the removal efficiency and enhance the practicality, potassium peroxymonosulfate (PMS) was added to the system due to its Fenton-like effect. Then, an Fe/Co/C composite was used with PMS to remove Congo red (CR) with a 98% removal of 250 mg·L−1. Moreover, for its high saturation magnetization of 85.4 emu·g−1, the Fe/Co/C composite can be easily recovered by applying a magnetic field, solving the problem that powdery functional materials are difficult to recover and, thus, avoiding secondary pollution. Furthermore, since the composite material was doped before carbonization, this synthetic strategy is flexible and the required metal elements can be added at will to achieve different purposes. This study demonstrates that this Fe-doped, ZIF-67 derived magnetic material has potential application prospects for dye adsorption. [ABSTRACT FROM AUTHOR]

High-salt printing and dyeing wastewater is a difficult industrial wastewater to treat. Coal-based activated carbon (CBAC) can be used as an adsorbent to treat high-salt printing and dyeing wastewater and realize the resource utilization of CBAC. In this study, simulated wastewater that contained methylene blue (MB) was used as the research object, and CBAC was used as the adsorbent. The effects of CBAC dosage, NaCl concentration, coexisting ions, adsorption time, MB concentration, humic acid concentration, and solution pH on the adsorption performance of CBAC with MB were discussed. The results showed that when the CBAC dosage was 0.6 g/L, the solution pH was greater than 6, the adsorption time was 8 h, the adsorption temperature was 308 K, and the MB concentration was 10 mg/L. Thus, the maximum adsorption capacity of CBAC with MB was obtained. The maximum adsorption capacity and removal rate were 15.5 mg/L and 90%, respectively. High-salt wastewater can inhibit the adsorption of methylene blue by coal-based activated carbon. In addition, 20 g/L of NaCl reduced the adsorption capacity of coal-based activated carbon by 1.8 mg/g. Compared to the other coexisting ions, the influence of the presence of Cu2+ and Fe3+ on the removal of methylene blue was greater. However, when Cu2+, Fe3+ and high-salt wastewater coexist, the inhibition effect decreases. [ABSTRACT FROM AUTHOR]

The green preparation of metal oxide nanoparticles is an environmentally friendly method, which could reduce the use of toxic solvents and their impact on the environment. The purpose of this study is to investigate the green synthesis of zinc oxide (ZnO) nanoparticles using extracts of Hibiscus cannabinus leaves and to evaluate their potential applications in environmental remediation. In this work, ZnO nanoparticles were successfully prepared and thoroughly characterized using UV–vis, Fourier transform infrared analysis (FTIR), X-ray diffraction (XRD), transmission electron microscope (TEM) analysis, and scanning electron microscope (SEM) with energy dispersive x-ray analysis (EDAX). As a result, the synthesized ZnO nanoparticles showed a good adsorption capacity for Congo red (CR), and satisfactory antioxidant and antibacterial activities. They exhibited good adsorption and removal abilities for CR in aqueous solutions. With the conditions optimized, the adsorption kinetics and isotherms were fitted to the pseudo-second-order model and the Langmuir model. The ZnO nanoparticles could also effectively scavenge 2-2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2′-azino-di(3-ethylbenzthiazoline sulphonate) (ABTS) radicals, and appeared to inhibit the growth of Escherichia coli and Staphylococcus aureus bacteria. Based on the identified adsorption capacity, the green synthesized ZnO nanoparticles demonstrated their potential to be used in the removal of dyeing wastewater and in the further purification of water due to their antioxidant activity and antibacterial activity. [ABSTRACT FROM AUTHOR]

A highly-efficient graphitic carbon nitride (g-C3N4) photocatalyst for visible light photodegradation of rhodamine B (RhB) and methyl orange (MO) simulating dyeing wastewater was synthesized by the thermal polycondensation of melamine. The photocatalysts were characterized by TG-DTG-DSC, XRD, EA, XPS, FT-IR, SEM, TEM, BET, PL and UV-vis DRS. The results showed that the photocatalytic performance of g-C3N4 at a higher calcination temperature was significantly enhanced, and its photocatalytic activities for the photodegradation of RhB and MO were remarkably improved by 64.91% and 41.83%, respectively, which was mainly attributed to the satisfactory crystallinity, stable graphene-like structure, large surface area, and excellent optical properties. It was found that •O2− radicals and •OH radicals were the main active species for the photodegradation process by the free radicals trapping experiments and ESR analysis. The photodegradation mechanism of g-C3N4 was proposed predicated using the characterization results. [ABSTRACT FROM AUTHOR]

One of the more problematic textile wastewaters to manage is dyeing wastewater, especially methylene-blue-containing wastewater. Its release has a significant negative impact on ecosystems, which could harm the environment. Adsorption techniques are still an efficient technology to eliminate and remove the coloring agent. Tailing ash, obtained from the floatation process, was selected as an adsorbent in the present study. The purpose of this study was to analyze the performance of tailing ash (TA) for MB removal. The effects of operating parameters investigated were pH (2–10), stirring speed (50–150 rpm), initial dye concentration (20–100 mg/L), contact time (120 min), adsorbent dosage (0.5–2.5 g), and temperature (25–45 °C). The performance of TA pretreated with hydrogen peroxide (H2O2) and thermal tailing ash were also investigated. The experimental results for batch adsorption indicated that 96.23% removal of methylene blue took place at the optimum condition (pH = 10, initial adsorbent dosage = 1.5 g, 150 rpm, contact time = 120 min, 45 °C). The results showed that the dye adsorption capacity increased with contact time and adsorbate dosage. The adsorption data were then fitted to kinetic models and isotherm models. The pseudo-second-order model was the most suitable model for the kinetic of adsorption and the Freundlich isotherm was the best-fitted isotherm model. This research provides a feasible approach to reusing tailing ash as an effective low-cost adsorbent for water quality improvement. [ABSTRACT FROM AUTHOR]

The organic dyes used in printing and dyeing wastewater have complex components, diverse structures and strong chemical stability, which make them not suitable for treatment and difficult to degrade in the environment. Porphyrins are macromolecules with 18 π electrons formed by four pyrrole molecules connected with a methylene bridge that has a stable structure. Porphyrin combines with iron to form an active intermediate with a structure similar to the cytochrome P450 enzyme, so they are widely used in the biomimetic field. In the current study, 5,10,15,20-tetra (4-carboxyphenyl) porphine ferric chloride (III) (Fe(III)TCPP) was used as a catalyst and iodosobenzene was used as an oxidant to explore the catalytic degradation of triphenylmethane dyes, such as rhodamine B (RhB) and malachite green (MG). The results of UV-Vis spectral analysis have shown that the conversion rate of the rhodamine B was over 90% when the amount of Fe(III)TCPP was 0.027 mM and the amount of iodosobenzene was eight equivalents. When the catalyst was 0.00681 mM and the amount of the oxidant was five equivalents, the conversion rate of the malachite green reached over 95%. This work provides a feasible method for the degradation of triphenylmethane dyes. [ABSTRACT FROM AUTHOR]

In this study, pristine kiwi peel (KP) and nitric acid modified kiwi peel (NA-KP) based adsorbents were prepared and evaluated for selective removal of cationic dye. The morphology and chemical structure of KP and NA-KP were fully characterized and compared, and results showed nitric acid modification introduced more functional groups. Moreover, the adsorption kinetics and isotherms of malachite green (MG) by KP and NA-KP were investigated and discussed. The results showed that the adsorption process of MG onto KP followed a pseudo-second-order kinetic model and the Langmuir isotherm model, while the adsorption process of MG onto NA-KP followed a pseudo-first-order kinetic model and the Freundlich isotherm model. Notably, the Langmuir maximum adsorption capacity of NA-KP was 580.61 mg g−1, which was superior to that of KP (297.15 mg g−1). Furthermore, thermodynamic studies demonstrated the feasible, spontaneous, and endothermic nature of the adsorption process of MG by NA-KP. Importantly, NA-KP showed superior selectivity to KP towards cationic dye MG against anionic dye methyl orange (MO). When the molar ratio of MG/MO was 1:1, the separation factor (αMG/MO) of NA-KP was 698.10, which was 5.93 times of KP. In addition, hydrogen bonding, π-π interactions, and electrostatic interaction played important roles during the MG adsorption process by NA-KP. This work provided a low-cost, eco-friendly, and efficient option for the selective removal of cationic dye from dyeing wastewater. [ABSTRACT FROM AUTHOR]

Intending to provide efficient and compact wastewater remediation, the present work is exploiting and introducing a novel composite prepared from porous starch aerogel (PSA) and organically modified Ca-montmorillonite (OMMT) for the removal of dyes from aqueous samples. First, potato starch components were used as a hydrolysis precursor to obtain PSA. The organoclay samples were prepared by co-intercalation of octadecylamine (ODA) into Ca-MMT using a low-temperature melting procedure. Composites with different starch-to-organoclay ratios of 10:1, 1:1, and 1:10 were then prepared by a blending process in distilled water and used for methyl orange (MO) uptake. The removal of methyl orange dyes increased with the amount of organoclay in the PSA matrix. Characterization revealed that organoclay synergy improved the PSA surface chemistry, while an important improvement in textural properties and thermal stability was also observed. The composite's efficiency was demonstrated by high removal capabilities towards MO in most experimental runs, with a maximum adsorption capacity beyond 344.7 mg/g. The fitting result showed that MO adsorption follows a monolayer adsorption model, and chemisorption was the rate-controlling step. Nonetheless, this study proved the great potential of PSA/OMMT in dyeing wastewater treatment. Furthermore, starch modification is proven as an effective approach to enhancing the performance of starch-derived adsorbents. [ABSTRACT FROM AUTHOR]

The comprehensive utilization of low-grade diatomite resources and the effective treatment of printing and dyeing wastewater have attracted widespread attention. The combined scrubbing-magnetic separation-acid leaching-roasting process was used to increase the SiO2 content from 59.22% to 86.93%, reduce the Al2O3 content from 18.32% to 6.75%, and reduce the Fe2O3 content from 6.85% to 1.24% in the low-grade diatomite from Heilongjiang, China. The TiO2/g-C3N4/diatomite nanocomposite was prepared by a facile ultrasonic-thermal polymerization method. In this ternary structure, diatomite skeleton effectively increased the surface area with abundant adsorption sites, prevented g-C3N4 from restacking, and facilitated the separation of electrons and holes via the formation of TiO2/g-C3N4 heterojunctions. The degradation rate was 98.77%, 90.59%, and 89.16% for the three catalytic reaction cycles of the MB solution, respectively. The composite showed a high degradation rate of the MB solution after three cycles, which indicated that the composite had good recyclability. Through the free radical capture test, it was elucidated that O2−·, h+, and ·OH all played a role in the photocatalytic reaction of the TiO2/g-C3N4/diatomite to the MB solution, in which O2−· was mainly responsible for the photocatalytic oxidation mechanism, and the reaction kinetics were further investigated. This nanostructured TiO2/g-C3N4/diatomite composite has fascinating visible light catalytic activity and excellent stability. [ABSTRACT FROM AUTHOR]

Untreated textile effluent may contain toxic organic pollutants that can have negative impacts on the ecosystem. Among the harmful chemicals present in dyeing wastewater, there are two frequently used organic dyes: methylene blue (cationic) and congo red (anionic). The current study presents investigations on a novel two-tier nanocomposite membrane, i.e., a top layer formed of electrosprayed chitosan–graphene oxide and a bottom layer consisting of an ethylene diamine functionalized polyacrylonitrile electrospun nanofiber for the simultaneous removal of the congo red and methylene blue dyes. The fabricated nanocomposite was characterized using FT-IR spectroscopy, scanning electron microscopy, UV-visible spectroscopy, and Drop Shape Analyzer. Isotherm modeling was used to determine the efficiency of dye adsorption for the electrosprayed nanocomposite membrane and the confirmed maximum adsorptive capacities of 182.5 mg/g for congo red and 219.3 mg/g for methylene blue, which fits with the Langmuir isotherm model, suggesting uniform single-layer adsorption. It was also discovered that the adsorbent preferred an acidic pH level for the removal of congo red and a basic pH level for the removal of methylene blue. The gained results can be a first step for the development of new wastewater cleaning techniques. [ABSTRACT FROM AUTHOR]

Adsorption is one of the most promising decolorization techniques in dyeing wastewater treatment. Adsorption techniques for wastewater treatment have become more popular in recent years owing to their efficiency in the removal of pollutants too stable for biological methods. Dye adsorption is a result of two mechanisms (adsorption and ion exchange) and is influenced by many factors as dye/adsorbent interaction, adsorbent's surface area, particle size, temperature, pH, and contact time. The main advantage of adsorption recently became the use of low-cost materials, which reduces the procedure cost. The present review firstly introduced the technology process, research history and research hotspot of adsorption. Then, the application of adsorption in treatment of dyeing wastewaters in the past decades was summarized, revealing the impressive changes in modes, trends, and conditions. From this review article, the different philosophy of synthesis of adsorbent materials became evident. [ABSTRACT FROM AUTHOR]

In this study, novel chitosan/silica composites with different mass ratios were prepared by in-situ hydrolysis using chitosan (from shrimp shell) as a carrier, triblock copolymer (P123) as the structure-directing agent, and ethyl orthosilicate as a silicon source. These nanocomposites were characterized by different techniques, including the FT-IR, XRD, TGA, SEM, TEM and N2 adsorption–desorption. The results indicated that the morphology and properties of composites changed with the introduction of silica. When the CS/TEOS mass ratio was 0.0775, the CS−2/SiO2 composite displayed a coral-like three-dimensional porous structure with specific surface area of 640.37 m2/g and average pore size of 1.869 nm. The adsorption properties for methylene blue (MB) were investigated as well and the CS−2/SiO2 showed better adsorption performance. The removal rate for MB reached 94.01% with absorbents dosage of 6 g/L, initial concentration of 40 mg/L, initial pH value of 7, temperature of 35 °C, and adsorption time of 40 min. The adsorption process well fitted the Langmuir isothermal model and quasi-second-order adsorption kinetics model. The maximum adsorption capacity for MB was 13.966 mg/g based on Langmuir fitting. The surface functional groups of the composites can play an important role in the adsorption. The adsorption mechanism of CS−2/SiO2 on MB involved electrostatic interaction, hydrogen bonding and functional group complexation. In addition, the prepared chitosan/silica composites showed good reusability at six cycles, making them a promising material in the application of removing dyeing wastewater. [ABSTRACT FROM AUTHOR]

Organic dyes are widely used in the textile, biological, medical and other fields. However, a serious environmental problem has appeared because of the presence of organic dyes in industrial aqueous effluents. Thus, the efficient treatment of organic dyes in industrial wastewaters is currently in real demand. The current study investigated the oxidative degradation of the organic dye gentian violet by meso-tetra(carboxyphenyl) porphyriniron(III), [FeIII(TCPP)] as a cytochrome P450 model and iodosylbenzene (PhIO) as an oxidant at room temperature. The degradation reaction was monitored by UV–vis absorption spectroscopy via the observation of UV–vis spectral changes of the gentian violet. The results showed that the efficiency of catalyzed degradation reached more than 90% in 1 h, indicating the remarkable oxidative degradation capacity of the [FeIII(TCPP)]/PhIO system, which provided an efficient approach for the treatment of dyeing wastewater. [ABSTRACT FROM AUTHOR]