Contaminants In Industrial Wastewater Research Articles

Adsorption of cationic dye onto Raphanus seeds: optimization, adsorption kinetics, thermodynamic studies

Dyes are one of the common contaminants in industrial wastewater. Adsorption is the most widely method which used to treat dye-contaminated water due to their easy use, cost-effectiveness, and their efficiency was high. The aim of this study is the investigating of the utilization of the activated carbon which prepared from Raphanus seeds solid residual (ACRS) as a low cost adsorbent for removing of cationic Methylene Blue dye (MB)from wastewater. measuring the surface area using BET methods and SEM. The FT‒IR and XRD was measured. Different variables (e.g.: initial concentration of the dye, pH, contact time, and dosage) have been studied. Process has been systematically investigated experimentally at (25 ± 1 °C). The % removal of MB reached 99.4% after 90-min MB adsorption (40 mg/L) was observed within 5 min of contact time for the Raphanus seeds solid residual (ACRS) dosage of 4 g/L. MB initial concentration (10 ppm) Raphanus seeds solid residual (ACRS) effectively adsorbed MB (> 99%) over a widely range of pH (from pH 2 to pH 8). However, a swift decline in removal was observed when the pH was set at 7. The results of the adsorption kinetics analysis indicate a strong correlation with the pseudo-second-order model, as evidenced by the high regression coefficients. However, the adsorption capacity diminished with a rise in temperature. Thermodynamic calculations of (MB) onto Raphanus seeds solid residual (ACRS) is an exothermic reaction. The results have been indicated that the effectiveness of MB removal by activated carbon prepared from Raphanus seeds solid residual is favorable under neutral conditions, Raphanus seeds solid residual (ACRS) can be considered an efficient, environmentally friendly, readily available, and economical adsorbent that could treat industrial wastewater contaminated with cationic textile dyes. The objective of the experiments was to investigate the impact of various factors on the response of a process or formulation. To accomplish this goal, response surface methodology (RSM) has employed as a statistical model. RSM is an efficient and effective method for optimizing processes through the use of a quadratic polynomial model. The utilization of RSM allows for a reduction in the number of experiments needed, thus minimizing the associated costs of extensive analysis. This method has been done using Box–Behnken Design (BBD) to optimize % removal of MB. The optimal conditions as obtained from the RSM is pH 7,contact time 120 min, initial concentration 10 ppm, ACRS dosage 1 g, adsorption temperature 45 °C.

Enhancing methyl violet 2B pollutant removal from wastewater using Al-MOF encapsulated with poly (itaconic acid) grafted crosslinked chitosan composite sponge: Synthesis, characterization, DFT calculation, adsorption optimization via Box-Behnken Design

In this research, aluminum metal-organic framework encapsulated with poly (itaconic acid) grafted crosslinked chitosan composite sponge (Al-MOF@PIC) was prepared. SEM, FTIR, XPS, XRD, and BET techniques were employed to thoroughly characterize the synthesized material and establish its structure and characteristics. The study discovered that the Al-MOF@PIC is an efficient way to remove dyes, which constitute a significant number of contaminants in industrial wastewater. Subsequently the adsorption of methyl violet 2B (MV-2B) dye, the surface area, pore size, and pore volume of the adsorbent decreased from 1860.68 m2/g, 1.62 nm, and 1.52 cc/g to 1426.45 m2/g, 1.11 nm, and 0.92 cc/g, individually. This modification suggested that a portion of the MV-2B dye had been removed by adsorption over the adsorbent's pores. The excellent adsorption capacity of the material was further confirmed by batch adsorption tests, which displayed a maximum adsorption capability of 646.76 mg/g for the elimination of MV-2B dye. The high adsorption energy of 26.8 kJ/mol designates that chemisorption is primarily responsible for MV-2B dye adsorption against the sponge adsorbent. The Al-MOF@PIC composite sponge demonstrated exceptional reusability over six cycles, demonstrating its strength and durability. The Al-MOF@PIC composite sponge successfully removes MV-2B from water by pore filling, π-π stacking, hydrogen bonding, and electrostatic interactions, which are the key mechanisms behind the adsorption of the dye pollutant. Its potential for practical applications is further demonstrated using Box Behnken-design (BBD) to optimize the adsorption consequences.

Musa acuminata free tepal (MAFT) crop- mediated synthesis of copper oxide nanocatalyst (MAFT-CuO nanocatalyst): Investigation of aerobic oxidation and dye decolourization via eco-friendly approach

Crop development is used to address environmental problems in the industry. Environmental pollutants, particularly humble or toxic chemicals and dyes, are contaminants in industrial wastewater. Recently, green technology has become important for controlling the chemical risks associated with environmental issues. This study focused on valuable crop materials to form green catalysts that can be used to control chemical toxicity in industrial wastewater. In this study, Musa acuminata-free tepal (MAFT) crops and musa were used to mediate the formation of copper nanocatalyst for environmental pollution. The synthesised nanocatalyst was analysed by XPS, XRD, TEM, SEM, FT-IR, GC-EI-MS, and TGA-DSC. The production of Cu–O in the 512 cm−1 peak range was verified by FT-IR analysis. The XRD peaks associated with the cubic crystalline structures of copper (110) and (200) were used to confirm the Musa acuminata-free tepal CuO nanocatalyst. The SEM images of the Cu and CuO nanocatalyst in the Musa acuminata free tepal showed that the particles were almost spherical. The size of the synthesised Musa acuminata free tepal CuO nanocatalyst core-shell nanostructures was identified using HR-TEM. GC-MS investigations also verified the aerobic oxidation of the main alcohol to aldehyde, with a retention time of 30.34. The MAFT was 80 % of CBB G250 dye decolourised at 24 h, and the MAFT-CuO nanocatalyst was decolourised the CBB G250 dye at 80 % in 20 min and aerobic oxidation at the same time (dual application). Furthermore, our nanocatalyst could be effectively recycled without significant loss of catalytic activity, and the use of safe, environmentally benign MAFT-Cu and CuO nanocatalyst is considered a green chemistry approach that helps avoid wastewater treatment. MAFT-Cu and CuO nanocatalyst were successfully synthesised using Musa acuminata free tepal extract assisted by reflux sample preparation system instruments as a new, green, eco-friendly, and fast process for nanocatalyst synthesis. In the past, there have been no reported applications of MAFT-Cu and CuO nanocatalyst for decolourisation and aerobic oxidation. Nevertheless, we were able to accomplish these procedures with the help of CuO and MAFT-Cu nanocatalyst. Therefore, the most effective naturally occurring environmental catalysts for aerobic oxidation processes are MAFT-CuO nanocatalyst. They are non-toxic and environmentally benign, exhibit strong aerobic oxidation catalytic performance, and have long-lasting benefits for water quality. Additionally, they are more recoverable and biodegradable.

Functionalization of cellulose acetate nanofibrous membranes for removal of particulate matters and dyes

Particulates and organic toxins, such as microplastics and dye molecules, are contaminants in industrial wastewater that must be purified due to environmental and sustainability concerns. Carboxylated cellulose acetate (CTA-COOH) nanofibrous membranes were fabricated using electrospinning followed by an innovative one-step surface hydrolysis/oxidation replacing the conventional two-step reactions. This approach offers a new pathway for the modification strategy of cellulose-based membranes. The CTA-COOH membrane was utilized for the removal of particulates and cationic dyes through filtration and adsorption, respectively. The filtration performance of the CTA-COOH nanofibrous membrane was carried out; high separation efficiency and low pressure drop were achieved, in addition to the high filtration selectivity against 0.6-μm and 0.8-μm nanoparticles. A cationic Bismarck Brown Y, was employed to challenge the adsorption capability of the CTA-COOH nanofibrous membrane, where the maximum adsorption capacity of the membrane for BBY was 158.73 mg/g. The self-standing CTA-COOH membrane could be used to conduct adsorption-desorption for 17 cycles with the regeneration rate as high as 97.0 %. The CTA-COOH nanofibrous membrane has excellent mechanical properties and was employed to manufacture a spiral wound adsorption cartridge, which exhibited remarkable separation efficiency in terms of treated water volume, which was 5.96 L, and retention rate, which was 100 %.

Evaluating the effects of pH and temperature on sulphate-reducing bacteria and modelling of their effects in stirred bioreactors

ABSTRACT Sulphate (SO4) abundance in the earth’s crust contributes largely to industrial wastewater contamination lowering the pH, which exuberates the dissolution of metals forming acidic drainages. Biological sulphate reduction as a remediation process can be affected by factors such as pH, temperature and high sulphide concentrations. In this study, sulphate-reducing bacterial community enriched from mine wastewaters was applied in semi-automated bioreactors to assess the effects of these factors on microbial sulphate reduction capacities. Low pH (3.5) and temperature (10°C) were observed to promote the toxicity of sulphur-reduced species on the consortium while mesophilic temperature (25°C) and near neutral pH (6.2) were observed to induce optimum SO4 reduction attaining a maximum of 95% SO4 reduction. Obtained SO4 reduction dynamics data was then applied in formulating a unique non-competitive inhibition equation that models biogeochemical events during SO4 reduction under varied pH and temperature conditions and predicts the efficacy of a bioremediation system.

Electrochemical oxidation and sensing of para benzoquinone using a novel SPE based disposable sensor

Para-benzoquinone (PBQ) is an emerging micro-contaminant owing to its chronic toxicity to plants and animals as well as its potential to induce cytotoxicity in primary rat hepatocytes and kidney cell injury. Hence, it is of utmost importance to monitor this contaminant in industrial wastewater and groundwater. In this article, we devised a unique disposable sensor that is based on a screen-printed electrode using MnO2@Co–Ni MOFs/fMWCNTs nanocomposite and is able to detect PBQ. The as-produced nanocomposite was prepared via ultrasonic assisted reflux condition and thoroughly examined by several physicochemical characterisation methods such as SEM, EDX, TEM, Raman, AFM, UV–visible, and FT-IR. Moreover, electrochemical methods like CV, DPV, EIS, and chronoamperometry were used for detecting PBQ on MnO2@Co–Ni MOFs/fMWCNTs/SPCE. Sensor performance has been investigated thoroughly and optimized to enhance the analytical potential of the fabricated sensor. DPV analysis was done on MnO2@Co–Ni MOFs/fMWCNTs that exhibit high selectivity, low peak potential, a broader linear detection range (0.005 mM–30 mM), and a LOD of 0.0027 ± 0.0005 mM. The designed electrode has shown remarkable reproducibility and excellent repeatability, with relative standard deviations of 0.12%, and 0.17%, respectively. Additionally, MnO2@Co–Ni MOFs/fMWCNTs/SPCE have been used to analyse PBQ in industrial wastewater samples, and the results have shown a significant level of recovery between 96.91 and 105.67%. Moreover, the PBQ sensor displays high applicability and was verified via the use of HPLC techniques. This disposable sensor is quick, easy, and cost-effective, so it can be useful in the future for analysing other phenolic contaminants present in environmental samples.

Challenges of Distillery Effluent Treatment and its Bioremediation Using Microorganism: A Review.

Waste management is a global issue with which the entire globe is currently grappling. The composition and characteristics of the pollutants in effluents are unknown, which poses the greatest worry. The Industrial Revolution has captured the attention of environmentalists worldwide. Their concern regarding the lethal effects of untreated industrial effluent wastewater is growing daily. Dealing with a range of hazardous compounds is costly and complicated, which hinders wastewater treatment. Recent years have paved the way for microorganisms to act as a low-cost source for detoxifying such a complex effluent mixture. Their simple availability and moderate cost make them the preferred technique. Bioremediation is the method of utilising the high and diversified metabolic activity of microorganisms to breakdown contaminants in industrial wastewater, particularly distillery effluent. Their readily available nature and affordable price make them the preferred option. Bioremediation is the process of using bacteria and other organisms with strong metabolic activity to breakdown contaminants in industrial effluents, particularly distillery effluents. Microorganisms like Bacteria fungi etc.,alone or in conjunction with other organisms, create an environment conducive to not only the breakdown of toxicants but also the production of some useful byproducts. This review focuses on distillery effluents, particularly melanoidins, and the reported microorganisms utilised for decolorization. The study combines a vast array of microorganisms that are utilised alone or in conjunction with other organisms in the decolorization process.

Is cavitation a truly sensible choice for intensifying photocatalytic oxidation processes? – Implications on phenol degradation using ZnO photocatalysts

Phenols are recalcitrant compounds that constitute the majority of organic contaminants in industrial wastewaters. Their removal at large scales require a combination of various processes to reach the desired discharge quality. An extensive body of work has already been published in the area of phenol removal from wastewater, however none of them have focussed on a truly ‘sensible’ approach for coupling advanced oxidation processes (AOPs). Rather, a higher removal efficiency was targeted by unduly complicating the process by combining multiple AOPs. The most influential AOP as the primary method typically driven by the nature of the pollutant should form the basis for a hybrid AOP followed by a complementary AOP to intensify the oxidation process. This strategy is lacking in current literature. We address this knowledge gap directly by systematically identifying the best hybrid process for ZnO mediated photocatalysis of phenol. Either a cavitation mediated pre-treatment of ZnO or cavitation-photocatalysis-peroxide based hybrid AOP was investigated. While the pre-treatment approach led to >25% increase in phenol oxidation compared to bare ZnO photocatalysis, the hydrodynamic cavitation-photocatalysis-peroxide based system was found to have a cavitational yield 5 times higher than its acoustic cavitation counterpart. A new phenomenon known as the ‘pseudo staggered effect’ was also observed and established in hydrodynamic cavitation mediated photocatalysis-peroxide hybrid process for the first time. While we demonstrated that cavitation is a truly ‘sensible’ choice to enhance photocatalysis, the nature of the pollutant under investigation must always be the key driver when designing such hybrid AOPs.

Biological treatment solutions using bioreactors for environmental contaminants from industrial waste water

AbstractHuman needs have led to the development of various products which are produced in the industries. These industries in turn have become a source of various environmental concerns. As industries release regulated and unregulated contaminants into the water bodies, it has become a serious concern for all living organisms. Various emerging contaminates from industries like pesticides, pharmaceuticals drugs like hormones, antibiotics, dyes, etc., along with byproducts and new complexes contaminate the water bodies. Numerous traditional approaches have been utilized for the treatment of these pollutants; however, these technologies are not efficient in most cases as the contaminants are mixed with complex structures or as new substances. Advanced technologies such as bioreactor techniques, advanced oxidation processes, and so on have been used for the treatment of industrial wastewater and have served as an alternative way for wastewater treatment. Overall, biological treatment techniques based on bioreactors provide a long-term and ecologically useful solution to industrial wastewater contamination. They play an important role in saving water resources and encouraging a greener sustainable future for mankind. The current review outlines the industrial effluents that are released into water bodies, contaminating them, as well as the numerous traditional and novel treatment procedures used for industrial wastewater treatment. Graphical abstract

Degradation of tartrazine by Oxone® in the presence of cobalt based catalyst supported on pillared montmorillonite - Efficient technology even in extreme conditions

The catalytic degradation of hazardous organic contaminants in industrial wastewater is a promising technology. Reactions of tartrazine, the synthetic yellow azo dye, with Oxone® in the presence of catalyst in strong acidic condition (pH 2), were detected by using UV–Vis spectroscopy. In order to extend the applicability profile of Co-supported Al-pillared montmorillonite catalyst an investigation of Oxone® induced reactions were performed in extreme acidic environment. The products of the reactions were identified by liquid chromatography–mass spectrometry (LC-MS). Along with the catalytic decomposition of tartrazine induced by radical attack (confirmed as unique reaction path under neutral and alkaline conditions), the formation of tartrazine derivatives by reaction of nucleophilic addition was also detected. The presence of derivatives under acidic conditions slowed down the hydrolysis of tartrazine diazo bond in comparison to the reactions in neutral environment. Nevertheless, the reaction in acidic conditions (pH 2) is faster than the one conducted in alkaline conditions (pH 11). Theoretical calculations were used to complete and clarify the mechanisms of tartrazine derivatization and degradation, as well as to predict the UV–Vis spectra of compounds which could serve as predictors of certain reaction phases. ECOSAR program, used to estimate toxicological profile of compounds to aquatic animals, indicated an increase in the harmfulness of the compounds identified by LC-MS as degradation products from the reaction conducted for 240min. It could be concluded that an intensification of the process parameters (higher concentration of Oxone®, higher catalyst loading, increased reaction time, etc.) is needed in order to obtain only biodegradable products.

Recycling of waste aluminum scraps to fabricate sulfidated zero-valent iron-aluminum particles for enhanced chromate removal

Massive waste aluminum scraps produced from the spent aluminum products have high electron capacity and can be recycled as an attractive alternative to materials based on zero-valent iron (Fe0) for the removal of oxidative contaminants from wastewater. This study thus proposed an approach to fabricate micron-sized sulfidated zero-valent iron-aluminum particles (S-Al0@Fe0) with high reactivity, electron selectivity and capacity using recycled waste aluminum scraps. S-Al0@Fe0 with a three-layer structure contained zero-valent aluminum (Al0) core, Fe0 middle layer and iron sulfide (FeS) shell. The rates of chromate (Cr(VI)) removal by S-Al0@Fe0 at pH 5.0‒9.0 were 1.6‒5.9 times greater than that by sulfidated zero-valent iron (S-Fe0). The Cr(VI) removal capacity of S-Al0@Fe0 was 8.2-, 11.3- and 46.9-fold greater than those of S-Fe0, zero-valent iron-aluminum (Al0-Fe0) and Fe0, respectively. The chemical cost of S-Al0@Fe0 for the equivalent Cr(VI) removal was 78.5% lower than that of S-Fe0. Negligible release of soluble aluminum during the Cr(VI) removal was observed. The significant enhancement in the reactivity and capacity of S-Al0@Fe0 was partially ascribed to the higher reactivity and electron density of the Al0 core than Fe0. More importantly, S-Al0@Fe0 served as an electric cell to harness the persistent and selective electron transfer from the Al0-Fe0 core to Cr(VI) at the surface via coupling Fe0-Fe2+-Fe3+ redox cycles, resulting in a higher electron utilization efficiency. Therefore, S-Al0@Fe0 fabricated using recycled waste aluminum scraps can be a cost-effective and environmentally-friendly alternative to S-Fe0 for the enhanced removal of oxidative contaminants in industrial wastewater.

Enhanced removal of metal-cyanide complexes from wastewater by Fe-impregnated biochar: Adsorption performance and removal mechanism

Metal-cyanide complexes are common contaminants in industrial wastewater. Removal of these refractory contaminants is essential before their discharge into the environment. This study investigated a biochar (BC)-based sorbent material that could be applied for the efficient removal of metal-cyanide complexes from wastewater. In consideration of the strong electrostatic repulsion of the pristine BC toward anions, iron-modified BC (Fe-BC) composites were fabricated by a one-step co-pyrolysis of corn straw and FeCl3 at 600–800 °C. The adsorption performance and corresponding sorption mechanisms of representative metal-cyanide complexes (ferricyanide [Fe(CN)6]3- and tetracyanonickelate [Ni(CN)4]2-) onto the Fe-BC composites were investigated. The results indicated that the Fe-BC composites had significantly high affinity toward the metal-cyanide complexes, reaching a maximum sorption capacity of 580.96 mg/g for [Fe(CN)6]3- and 588.86 mg/g for [Ni (CN)4]2-. A mechanistic study revealed that Fe-impregnation during BC fabrication could effectively alter the negatively charged BC surface, forming more functional groups that could interact with the metal-cyanide complexes. Moreover, the transformation of carbon structure promoted the carbothermal reduction process, leading to the formation of various reductive-Fe minerals in the resulting Fe-BC composites. These modification-induced alterations to the surface and structural characteristics of BC were expected to facilitate the adsorption/precipitation of target contaminants. Different sorption mechanisms were proposed for the two metal-cyanide complexes that were the focus of this study. For [Fe(CN)6]3-, precipitation by Fe-bearing species in the Fe-BC composites was the major factor controlling [Fe(CN)6]3- removal, while for [Ni(CN)4]2- hydrogen bonding interactions between surface functional groups (especially hydroxyl (-OH) and carboxyl (-COOH)) and [Ni(CN)4]2- were the main factors controlling removal.

Evaluation and remediation protocol of selected organochlorine pesticides and heavy metals in industrial wastewater using nanoparticles (NPs) in Nigeria

Limited knowledge of the level of contaminants in industrial wastewater within the Nigerian states together with the global challenge of water supply have compelled our investigation into the analyses and removal of organochlorine pesticides (OCPs) and heavy metal contents in industrial wastewater. Wastewater samples were collected from 13 industries across five states in Nigeria. The OCPs content of the samples was extracted, cleaned up and analysed using gas chromatography-mass spectrometry. The results indicate that the mean concentrations of the OCPs in the effluent samples ranged from 1.76 ng L−1 (Dieldrin) to 0.89 ng L−1 (endrin). Cadmium (Cd), chromium (Cr) and lead (Pb) were evaluated in all the effluent water samples. The results show that the average concentrations of the heavy metal ions in the effluent samples ranged from 0.008 ± 0.003 mg L−1 (Cd) to 2.215 ± 0.841 mg L−1 (Pb). For the removal of the identified contaminants, biomagnetite nanoparticles (BioMag), magnetite nanoparticles (MagNPs), biomagnetite-CMC nanocomposite (BioMag-CMC) and magnetite-CMC nanocomposite (MagNPs-CMC) were synthesised and characterised using Braunauer–Emmett–Teller (BET), Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and high resolution-transmission electron microscopy (HR-TEM). This study demonstrates the successful application of nanoparticles (NPs) and nanocomposites in the removal of OCPs and heavy metal ions in industrial effluents. The routine assessment and continuous removal become important to attain a state of clean and healthy aquatic ecosystem due to rapid industrial and technological advances.

Selective NOx- Electroreduction to Ammonia on Isolated Ru Sites.

Nitrate and nitrite (NOx-) are widespread contaminants in industrial wastewater and groundwater. Sustainable ammonia (NH3) production via NOx- electroreduction provides a prospective alternative to the energy-intensive industrialized Haber-Bosch process. However, selectively regulating the reaction pathway, which involves complicated electron/proton transfer, toward NH3 generation relies on the robust catalyst. A specific consideration in designing selective NOx--to-NH3 catalysts should meet the criteria to suppress competing hydrogen evolution and avoid the presence of neighboring active sites that are in favor of adverse N-N coupling. Nevertheless, efforts in this regard are still inadequate. Herein, we demonstrate that isolated ruthenium sites can selectively reduce NOx- into NH3, with maximal Faradaic efficiencies of 97.8% (NO2- reduction) and 72.8% (NO3- reduction) at -0.6 and -0.4 V, respectively. Density functional theory calculations simulated the reaction mechanisms and identified the *NO → *NOH as the potential rate-limiting step for NOx--to-NH3 conversion on single-atom Ru sites.

Improving nanofiltration performance using modified cellulose nanocrystal-based TFN membranes

Heavy metal ions are one of the principal contaminants in industrial wastewater. Their removal in nanofiltration processes using thin-film nanocomposite (TFN) membranes is a promising treatment method. l-cysteine functionalized cellulose nanocrystals (CysCNCs) and acetylated CNCs (ACNCs) were synthesized via an iodine-catalyzed method. The successful modification of CNCs was confirmed using ATR-FTIR and 13C NMR spectroscopy. The modified CNCs were used in the synthesis of TFN membranes. Prior to interfacial polymerization, the CNCs were dispersed into the organic monomer solution (trimesoyl chloride in n-hexane) rather than in the aqueous monomer solution (piperazine), contrary to conventional practice.Membrane performance was assessed for thin film composite (TFC) and CNC, ACNC and CysCNC-TFN membranes. A simultaneous increase in water permeability/salt and heavy metal rejection of ACNC-TFNs and CysCNC-TFNs was observed. In heavy metal removal tests, the CysCNC-TFN0.2 membranes exhibited the highest water permeability (16 L/m2 h bar) compared to the ACNC-TFN0.1 membranes (14.5 L/m2 h bar), the CNC-TFN0.1 membranes (11.5 L/m2 h bar), and the TFC membranes (6 L/m2 h bar). The heavy metal rejections ranged from 89.2 to 98.4% for the copper ions and 87.0–95.2% for the lead ions, in the same order as for the water permeability results. Therefore, the water permeability/selectivity trade-off was overcome. The TFN membrane performance improvements were mainly attributed to both the nanoparticle functionality and their uniform distribution in the polyamide layer via their dispersion in the organic monomer solution.

An easily-synthesized low carbon ionic liquid functionalized metal-organic framework composite material to remove Congo red from water

Congo red (CR) is documented as a typical azo dye compound that is widely used for industrial activities such as papermaking, textiles, leather and additives production, making it a main component of COD contaminants in industrial wastewaters. Excessive releases of CR have resulted in adverse impacts on water environments and ecological systems due to its non-biodegradable, toxic and carcinogenic properties. Therefore, the removal of CR from water environments is of important for wastewater treatment. Previous studies have proved that metal-organic frameworks (MOFs) were feasible for CR adsorption, but less stable in water environments. Several functionalized materials have therefore been used to produce MOF-derived composite material for better performance. To simplify the synthesis processes and reduce the energy consumption, an ionic liquid (IL) was used in this study for the synthesis of [BMIM][PF6]/ZIF-8 (BP/Z) composite material. The morphological structure of this material remained stable after the incorporation of IL. The equilibrium time of CR adsorption was 90 ​min with a maximum adsorption capacity of 1463 ​mg/g. Isotherm and kinetic studies revealed that the adsorption process was better described by Langmuir and pseudo-second-order model. Our results also presented that the IL/MOF composite material can be used within pH 5 and 6 with the presence of Na+, K+, Mg2+, Ca2+, Cl− and SO42−. It was also proved that the novel IL/MOF composites in this study have great potential to adsorb and remove organic dyes from water.

Electrochemical biosensor based on tyrosinase-immobilized phase-change microcapsules for ultrasensitive detection of phenolic contaminants under in situ thermal management

Aiming at enhancing the detection of phenolic contaminants in high-temperature environments, we developed a thermoregulatory electrochemical biosensor based on the tyrosinase-immobilized electroactive phase-change microcapsules. The microcapsules were fabricated by engulfing n-eicosane as a phase-change material core in a TiO2 shell, followed by depositing with an electroactive hybrid layer comprising the polypyrrole matrix and tyrosinase-immobilized Fe3O4 nanoparticles. The resultant microcapsules show a well-defined core–shell microstructure and a regular spherical morphology, together with the desired chemical compositions and structures. Acting as a biosensing electrode material, the microcapsules exhibit a high latent heat capacity of around 150 J/g to implement microenvironmental temperature regulation for the biosensor through reversible phase transitions of their n-eicosane core. This enables the developed biosensor to obtain a higher enzyme activity and more sensitive biosensing performance at high assay temperatures when compared to conventional tyrosinase biosensors, resulting in a high sensitivity of 0.102 (µA·L)/µmol and a lower detection limit of 3.409 µmol/L for catechol detection. Based on a unique integration of phase-change microcapsules and immobilized tyrosinase in the working electrode, the electrochemical biosensor developed in this study has found a practical application for high-sensitive reorganization and high-accurate determination of phenolic contaminants in industrial wastewaters over a wide working temperature range.

Variation of the toxicity caused by key contaminants in industrial wastewater along the treatment train of Fenton-activated sludge-advanced oxidation processes

Industrial wastewater contains a mixture of refractory and hazardous pollutants that have comprehensive toxic effects. We investigated the treatment of a long-chain industrial wastewater treatment train containing Fenton, biological anoxic/oxic (AO), and heterogeneous ozone catalytic oxidation (HOCO) processes, and evaluated their detoxification effect based on the analysis of the genic toxicity of some key contaminants. The results showed that although the effluent met the discharge standard in terms of traditional quality parameters, the long-chain treatment process could not effectively detoxify the industrial wastewater. The analysis results of summer samples showed that the Fenton process increased the total toxicity and genotoxicity of the organics, concerned metals, and non-volatile pollutants, whereas the A/O process increased the toxicity of the organics and non-volatile pollutants, and the HOCO process led to higher toxicity caused by metals and non-volatile pollutants. The outputs of the winter samples indicated that the Fenton process reduced the total toxicity and genotoxicity caused by non-volatile pollutants but increased that of the organics and concerned metals. The effect of the A/O process on the effluent toxicity in winter was the same as that in summer, whereas the HOCO process increased the total toxicity and genotoxicity of the metals in winter samples. Correlation analysis showed that various toxicity stresses were significantly correlated with the variation of these key pollutants in wastewater. Our results could provide a reference for the optimization of industrial wastewater treatment plants (IWTPs) by selecting more suitable treatment procedures to reduce the toxicity of different contaminants.

Bioremediation potential of cadmium by recombinant Escherichia coli surface expressing metallothionein MTT5 from Tetrahymenathermophila

Cadmium (Cd) is a common heavy metal contaminant in industrial wastewater that causes many diseases in humans. Metallothionein (MT), a cysteine-rich metal-binding protein, is well known in chelate-heavy metals. In this study, we expressed MTT5 of Tetrahymena thermophila fused with Lpp-OmpA in the outer membrane of Escherichia coli to determine its ability to accumulate and adsorb Cd. Our results revealed that our recombinant E. coli had a 4.9-fold greater Cd adsorption compared to wild E. coli. Adsorption isothermic analysis demonstrated that the adsorption behavior for Cd in our recombinant bacteria was better fitted into the Freundlich isotherm model than Langmuir isotherm model. Fourier-transform infrared spectroscopy indicated that phosphate and organic phosphate groups were involved in the interaction between Cd and the bacterial surface. Using quantitative reverse transcription polymerase chain reaction, we further showed that the expression of metal-resistance genes (dnaK and clpB) was downregulated due to surface MTT5 protected our recombinant bacteria from Cd2+ adsorption. Furthermore, we showed that our recombinant bacteria could adsorb Cd from the contaminated wastewater containing other metals and were suggested to be applied in the field study.

Development of Co-Al LDH/GO composite photocatalyst for enhanced degradation of textile pollutant under visible light irradiation

Industrial wastewater contamination is a severe global issue due to the effective dosage of textile dyes that are directly exiting from the textile industries either without treatment or mild treatment. These dyes contain many organic pollutants severely damaging human beings along with aquatic environment and animals. Methylene blue (MB) dye is a carcinogenic that can cause acute diseases. In this regard, Photocatalysis proves an alluring approach because to its fascinating characteristics over ordinary technologies particularly economical and simple methodology. Layered double hydroxide (LDH) as a photocatalysts are exhibiting their promising performance for the treatment of organic pollutant in industrial wastewater. The present research displays a simple and facile co-precipitation method for the synthesis pure Co-Al LDH and its composite with graphene oxide (GO). A series of composites of GO and Co-Al layered doubled hydroxide with varied content of GO is successfully synthesized that enhanced the photocatalytic performance of Co-Al LDH in terms of MB dye degradation. With the optimized sample, 0.5 g GO loading onto Co-Al LDH termed as 0.5-CAL/GO, the MB dye degradation of 71 % was achieved under white LED light (10 W) irradiation. Synthesized photocatalysts are characterized by several analytical techniques such as (XRD, SEM, FTIR, Raman, UV Visible DRS, Photoluminescence spectroscopy). This research presents the flexible strategy for effective removal of MB dye simulated wastewater, acting as a textile industry wastewater employing a visible light active photocatalyst under white light (LED) illumination.