Upcycling crab shell waste into biochar for treatment of palm oil mill effluent via microwave pyrolysis and activation.

The escalating consumer demand for crabs results in a growing amount of waste, including shells, claws, and other non-edible parts. The resulting crab shell waste (CSW) is disposed of via incineration or landfills which causes environmental pollution. CSW represents a potential biological resource that can be transformed into valuable resources via pyrolysis technique. In this study, microwave pyrolysis of CSW using self-purging, vacuum, and steam activation techniques was examined to determine the biochar production yield and its performance in treating palm oil mill effluent (POME). The biochar produced through microwave pyrolysis exhibits yields ranging from 50 to 61 wt%, showing a hard texture, low volatile matter content (≤34.1 wt%), and high fixed carbon content (≥58.3 wt%). The KOH-activated biochar demonstrated a surface area of up to 177 m2/g that is predominantly composed of mesopores, providing a good amount of adsorption sites for use as adsorbent. The biochar activated with steam removed 8.3 mg/g of BOD and 42 mg/g of COD from POME. The results demonstrate that microwave pyrolysis of CSW is a promising technology to produce high-quality biochar as an adsorbent for POME treatment.

Synthesis of sustainable mesoporous sulfur-doped biobased carbon with superior performance sodium diclofenac removal: Kinetic, equilibrium, thermodynamic and mechanism.

Over the last years, the strategy of employing inevitable organic waste and residue streams to produce valuable and greener materials for a wide range of applications has been proven an efficient and suitable approach. In this research, sulfur-doped porous biochar was produced through a single-step pyrolysis of birch waste tree in the presence of zinc chloride as chemical activator. The sulfur doping process led to a remarkable impact on the biochar structure. Moreover, it was shown that sulfur doping also had an important impact on sodium diclofenac (S-DCF) removal from aqueous solutions due to the introduction of S-functionalities on biochar surface. The adsorption experiments suggested that General and Liu models offered the best fit for the kinetic and equilibrium studies, respectively. The results showed that the kinetic was faster for the S-doped biochar while the maximum adsorption capacity values at 318 K were 564 mg g-1 (non-doped) and 693 mg g-1 (S-doped); highlighting the better affinity of S-doped biochar for the S-DCF molecule compared to non-doped biochar. The thermodynamic parameters (ΔH0, ΔS0, ΔG0) suggested that the S-DCF removal on both adsorbents was spontaneous, favourable, and endothermic.

Mesoporogen free synthesis of CuO/TiO2 heterojunction for ultra-trace detection of catechol in water samples.

Creating mesoporous architecture on the surface of metal oxides without using pore creating agent is significant interest in electrochemical sensors because these materials act as an efficient electron transfer process between the electrode interface and the analytes. Recent advances in mesoporous titanium dioxide (TiO2)-based materials have acquired extraordinary opportunities because of their interconnected porous structure could act as a host for doping with various transition metals or heteroatoms to form a new type of heterojunction. Herein, a simple method is developed to synthesize mesoporous copper oxide (CuO) decorated on TiO2 nanostructures in which homogenous shaped CuO nanocrystals act as dopants decorated on the mesoporous structure of TiO2, resulting in p-n heterojunction nanocomposite. The TiO2 particles exhibit a mesoporous structure with a pore volume of about 0.117 cm3/g is capable to load CuO nanocrystals on the surface. As a result, large pore volume 0.304 cm³/g is obtained for CuO-TiO2 heterojunction nanocomposite with the loading of uniform-shaped CuO nanocrystals on the mesoporous TiO2. The resulting CuO-TiO2 nanocomposite on modified glassy carbon (GC) electrode exhibits good electrochemical performance for oxidation of catechol with the observation of strong enhancement in the anodic peak potential at +0.36 V. The decrease in the overpotential for the oxidation of catechol when compared to TiO2/GC is attributed to the presence of CuO nanocrystals providing a large surface area, resulting in wide linear range 10 nM to 0.57 µM. Moreover, the resultant modified electrode exhibited good sensitivity, selectivity and reproducibility and the sensor could able to determine the presence of catechol in real samples such as lake and river water. Therefore, the obtained CuO-TiO2 nanocomposite on the modified GC delivered good electrochemical sensing performance and which could be able to perform a promising strategy for designing various metal oxide doped nanocomposites for various photochemical and electrocatalytic applications.

"Magnetic Ni-Zn ferrite anchored on g-C3N4 as nano-photocatalyst for efficient photo-degradation of doxycycline from water".

In the present work, mixed-spinel ferrite anchored onto graphitic carbon nitride (GCN) was synthesized for mineralization of antibiotic pollutant from waste water. A Z-scheme g-C3N4/Ni0.5Zn0.5Fe2O4 nano heterojunction was fabricated by three step procedure: pyrolysis, solution combustion and mechanical grinding followed by annealing. The prepared photocatlyst was tested for degradation of Doxycycline (DC) drug under the natural sun light. Results revealed that the prepared heterojunction has maximum degradation efficiency of 97.10% pollutant in 60 min experiment. The Z-scheme heterojunction between g-C3N4 and Ni-Zn ferrite improves the photoinduced charges separation and protection of redox capability and therby increases the photo degradation efficiency. The scavenging experiments suggested that O2-● and h+ as main active species responsible for degradation of the antibiotic. In addition, the dopant variation can drive the shists in band gap and energy band positiong too which makes then excellent candidates for synthesizing tunable heterostructures with organic semiconductors. The work focusses on designing and developing of saimpler but efficient magnetic heterojunctions with superior redox capability for solar powered waste water treatment.

Autochthonous bioaugmentation accelerates phenanthrene degradation in acclimated soil.

Bioaugmentation helps to obtain a microbiome capable of remediating polycyclic aromatic hydrocarbons (PAHs). In this study, acclimation of microorganisms to soil supplemented with phenanthrene (PHE) led to enrichment with PAH-degraders, including those in Actinobacteriota and in the genera Streptomyces, Rhodococcus, Nocardioides, Sphingomonas, and Mycobacterium. Aqueous (28 °C, pH 6.5) and soil cultures inoculated with PHE-acclimated soil showed a high PHE (ca. 50 mg L-1) degradation efficiency. The PHE degradation kinetics in aqueous and soil incubations fitted to the Gompertz equation and the first-order kinetic equation, respectively. Indigenous microorganisms adapted to PHE in their environment, and this increased their capacity to degrade PHE. The effect of co-contaminants and pathway intermediates on PHE degradation showed that the degradation of PHE improved in the presence of diesel while being hindered by lubricant oil, catechol, salicylic and phthalic acid. Our findings provide theoretical and practical support for bioremediationof PAHs in the environment.

Degradation of levofloxacin from antibiotic wastewater by pulse electrochemical oxidation with BDD electrode.

Antibiotic-containing wastewater is a typical biochemical refractory organic wastewater and general treatment methods cannot effectively and quickly degrade the antibiotic molecules. In this study, a novel boron-doped diamond (BDD) pulse electrochemical oxidation (PEO) technology was proposed for the efficient removal of levofloxacin (LFXN) from wastewater. The effects of current density (j), initial pH (pH0), frequency (f), electrolyte types and initial concentration (c0(LFXN)) on the degradation of LFXN were systematically investigated. The degradation kinetics under four different processes have also been studied. The possible degradation mechanism of LFXN was proposed by Density functional theory calculation and analysis of degradation intermediates. The results showed that under the optimal parameters, the COD removal efficiency (η(COD)) was 94.4% and the energy consumption (EEC) was 81.43 kWh·m-3 at t = 120 min. The degradation of LFXN at pH = 2.8/c(H2O2) followed pseudo-first-order kinetics. The apparent rate constant was 1.33 × 10-2 min-1, which was much higher than other processes. The degradation rate of LFXN was as follows: pH = 2.8/c(H2O2) > pH = 2.8 > pH = 7/c(H2O2) > pH = 7. Ten aromatic intermediates were formed during the degradation of LFXN, which were further degraded to F-, NH4+, NO3-, CO2 and H2O. This study provides a promising approach for efficiently treating LFXN antibiotic wastewater by pulsed electrochemical oxidation with a BDD electrode without adding H2O2.

Adsorption of Omeprazole on Biobased Adsorbents Doped with Si/Mg: Kinetic, Equilibrium, and Thermodynamic Studies.

This paper proposes an easy and sustainable method to prepare high-sorption capacity biobased adsorbents from wood waste. A biomass wood waste (spruce bark) was employed to fabricate a composite doped with Si and Mg and applied to adsorb an emerging contaminant (Omeprezole) from aqueous solutions, as well as synthetic effluents loaded with several emerging contaminants. The effects of Si and Mg doping on the biobased material's physicochemical properties and adsorptive performance were evaluated. Si and Mg did not influence the specific surface area values but impacted the presence of the higher number of mesopores. The kinetic and equilibrium data presented the best fitness by the Avrami Fractional order (AFO) and Liu isotherm models, respectively. The values of Qmax ranged from 72.70 to 110.2 mg g-1 (BP) and from 107.6 to 249.0 mg g-1 (BTM). The kinetic was faster for Si/Mg-doped carbon adsorbent, possibly due to different chemical features provoked by the doping process. The thermodynamic data showed that the adsorption of OME on biobased adsorbents was spontaneous and favorable at four studied temperatures (283, 293, 298, 303, 308, 313, and 318 K), with the magnitude of the adsorption correspondent to a physical adsorption process (ΔH° < 2 kJ mol-1). The adsorbents were applied to treat synthetic hospital effluents and exhibited a high percentage of removal (up to 62%). The results of this work show that the composite between spruce bark biomass and Si/Mg was an efficient adsorbent for OME removal. Therefore, this study can help open new strategies for developing sustainable and effective adsorbents to tackle water pollution.

Statistical physics double-layer models for the experimental study and theoretical modeling of methyl orange dye adsorption on AlMnTiO nanocomposite.

A Al2O3/MnO2/TiO2 (AlMnTiO) nanocomposite was synthesized using the thermal coprecipitation method and the adsorption performance of methyl orange (MO) dye from aqueous solution was carried out. Single-parameter optimization was used to explore the properties of AlMnTiO nanocomposite parameters on dye adsorption, including dose of adsorbent, solution pH, contact duration, and starting MO concentration. The model is the appropriate adsorption isotherm for the equilibrium process using a pseudo-second-order kinetic model property. Langmuir plot had a Qmax (mg/g) of 198.4 and best fitted (R2=0.990) among different isotherm models. The relevant parameters were computed using the dual-energy binary-layer statistical physics model. The statistical physics binary-layer model yield n (stoichiometric coefficient) values of 0.410, 0.440, and 0.453, all values are below 1, demonstrating the multi-docking process. AlMnTiO nanocomposite was regenerated up to six times, making the material extremely cost-effective. Using AlMnTiO nanocomposite, MO dye was removed from wastewater both in the laboratory and on the industrial scale.

Valorization of fruit waste-based biochar for arsenic removal in soils.

Fruit waste disposal is a serious global problem with only 20% of such waste being routinely treated prior to discharge. Two of the most polluting fruit wastes are orange peel and walnut shell and new methods are urgently required to valorize such waste. In the present study, they where valorized via conversion into biochars at 500 °C (OPB500 for orange peel-based biochar produced at 500 °C and WaSB500 for walnut shell-based biochar produced at 500 °C), and evaluated for arsenic adsorption. A pore-rich surface morphology was observed with a low H/C ratio indicating high stability. Spectroscopic studies revealed the presence of minerals and surface functional groups (amide, carbonyl, carboxyl, and hydroxyl) suggesting high potential for arsenic immobilization. Adsorption studies revealed an arsenic removal efficiency of 88.8 ± 0.04% for WaSB500 exposed to initial arsenic concentration of 8 ppm for 5% biochar dose at 25 °C and 30 min contact time. In comparison, OPB500 showed slightly lower removal efficiency of 80.7 ± 0.1% (10 ppm initial concentration, 5% dose, 25 °C, 90 min contact time). Peak shifts in XRD and FTIR spectra together with isotherm, kinetic, and thermodynamic studies suggested arsenic sequestration was achieved via a combination of chemisorption, physisorption, ion exchange, and diffusion. The present investigation suggests valorization of fruit waste into thermo-stable biochars for sustainable arsenic remediation in dynamic soil/water systems and establishes biochar's importance for waste biomass minimization and metal (loid) removal from fertile soils.

Emerging contaminants of high concern for the environment: Current trends and future research.

Wastewater is contaminated water that must be treated before it may be transferred into other rivers and lakes in order to prevent further groundwater pollution. Over the last decade, research has been conducted on a wide variety of contaminants, but the emerging contaminants are those caused primarily by micropollutants, endocrine disruptors (EDs), pesticides, pharmaceuticals, hormones, and toxins, as well as industrially-related synthetic dyes and dye-containing hazardous pollutants. Most emerging pollutants did not have established guidelines, but even at low concentrations they could have harmful effects on humans and aquatic organisms. In order to combat the above ecological threats, huge efforts have been done with a view to boosting the effectiveness of remediation procedures or developing new techniques for the detection, quantification and efficiency of the samples. The increase of interest in biotechnology and environmental engineering gives an opportunity for the development of more innovative ways to water treatment remediation. The purpose of this article is to provide an overview of emerging sources of contaminants, detection technologies, and treatment strategies. The goal of this review is to evaluate adsorption as a method for treating emerging pollutants, as well as sophisticated and cost-effective approaches for treating emerging contaminants.

Emerging remediation potentiality of struvite developed from municipal wastewater for the treatment of acid mine drainage.

The valorisation of wastewaters for minerals recovery and their potential beneficiation has gained enormous attention recently. In this study the removal of phosphate and ammonia from municipal wastewater using activated magnesite resulted in the formation of struvite. The optimum conditions for the synthesis of struvite were 60 min of mixing, 300 rpm mixing speed, 1 g of activated magnesite and room temperature, whilst optimum conditions for the treatment of acid mine drainage (AMD) using the synthesized struvite were 45 min of mixing, 20 g of struvite dosage, 1000 mL, and 300 rpm mixing speed. The efficacy of struvite for neutralisation of AMD and attenuation of inorganic contaminants were ≥98.99% for metals (Al3+, Fe3+, and Mn2+) and ≥30% for SO42-. Traces of other metals such as Zn, Cu, Ni, Pb, and Cr were significantly attenuated. Phosphate was fully attenuated from the aqua-sphere. PHREEQC predicted the removal of minerals as oxy-(hydro)-sulphates, oxy-(hydro)-phosphate, metals hydroxides, and other complexes. FE-SEM equipped with FIB and an EDX, XRD, XRF, and FTIR confirmed the synthesis of struvite and fate of chemical species after treatment. This study confirmed the feasibility of recovering phosphate and ammonia as struvite which can be employed for the treatment of AMD.

Sustainable green nanoadsorbents for remediation of pharmaceuticals from water and wastewater: A critical review.

In the last three decades, pharmaceutical research has increased tremendously to offer safe and healthy life. However, the high consumption of these harmful drugs has risen devastating impact on ecosystems. Therefore, it is worldwide paramount concern to effectively clean pharmaceuticals contaminated water streams to ensure safer environment and healthier life. Nanotechnology enables to produce new, high-technical material, such as membranes, adsorbent, nano-catalysts, functional surfaces, coverages and reagents for more effective water and wastewater cleanup processes. Nevertheless, nano-sorbent materials are regarded the most appropriate treatment technology for water and wastewater because of their facile application and a large number of adsorbents. Several conventional techniques have been operational for domestic wastewater treatment but are inefficient for pharmaceuticals removal. Alternatively, adsorption techniques have played a pivotal role in water and wastewater treatment for a long, but their rise in attraction is proportional with the continuous emergence of new micropollutants in the aquatic environment and new discoveries of sustainable and low-cost adsorbents. Recently, advancements in adsorption technique for wastewater treatment through nanoadsorbents has greatly increased due to its low production cost, sustainability, better physicochemical properties and high removal performance for pharmaceuticals. Herein, this review critically evaluates the performance of sustainable green nanoadsorbent for the remediation of pharmaceutical pollutants from water. The influential sorption parameters and interaction mechanism are also discussed. Moreover, the future prospects of nanoadsorbents for the remediation of pharmaceuticals are also presented.

Removal of nutrients from pulp and paper biorefinery effluent: Operation, kinetic modelling and optimization by response surface methodology.

This study investigated the effectiveness of extended aeration system (EAS) and rice straw activated carbon-extended aeration system (RAC-EAS) in the treatment of pulp and paper biorefinery effluent (PPBE). RAC-EAS focused on the efficient utilization of lignocellulosic biomass waste (rice straw) as a biosorbent in the treatment process. The experiment was designed by response surface methodology (RSM) and conducted using a bioreactor that operated at 1-3 days hydraulic retention times (HRT) with PPBE concentrations at 20, 60 and 100%. The bioreactor was fed with real PPBE having initial ammonia-N and total phosphorus (TP) concentrations that varied between 11.74 and 59.02 mg/L and 31-161 mg/L, respectively. Findings from the optimized approach by RSM indicated 84.51% and 91.71% ammonia-N and 77.62% and 84.64% total phosphorus reduction in concentration for EAS and RAC-EAS, respectively, with high nitrification rate observed in both bioreactors. Kinetic model optimization indicated that modified stover models was the best suited and were statistically significant (R2 ≥ 0.98) in the analysis of substrate removal rates for ammonia-N and total phosphorus. Maximum nutrients elimination was attained at 60% PPBE and 48 h HRT. Therefore, the model can be utilized in the design and optimization of EAS and RAC-EAS systems and consequently in the prediction of bioreactor behavior.

Robust magnetic ZnO-Fe2O3 Z-scheme hetereojunctions with in-built metal-redox for high performance photo-degradation of sulfamethoxazole and electrochemical dopamine detection.

This work reports synthesis of a dual-function facile heterojunction and investigation of role of the charge transfer dynamism between individual semiconductor components for superior photocatalytic and electrochemical sensing application. The bio-benevolent and sturdy ZnO/Fe2O3 heterojunctions were utilized for visible light facilitated photo-degradation of sulfamethoxazole (SMX) antibiotic and electrochemical sensing of dopamine drug (DA). The fabricated heterojunction were characterized for structural, optical, and magnetic properties. Structural studies revealed the formation of nano heterojunction containing both phases. Magnetic studies confirmed the highly pure magnetic nature of photocatalysts. ZnO/30 wt%Fe2O3 heterojunction (S2) shows 95.2% SMX degradation under visible light and high retention of performance under solar light. The scavenging experiments infer that OH radicals are the active species responsible for degradation. A Z-scheme photocatalytic mechanism was predicted for higher performance with protection of high potential VB of ZnO and CB of Fe2O3 for high generation of reactive oxygen species. LC-MS was employed to predict a plausible degradation route. The sample modified glassy carbon electrodes (GCE) were used for electrochemical sensing of dopamine via cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The S2 junction exhibited 0.18 µM limit of detection with concentration range of 1 µM-50 µM. The stability test was successfully carried out at room temperature for 15 days. In addition, the S2 modified electrodes were spiked in real urine samples and good results were obtained. DPV reveals that S2 modified electrode is best sensor for dopamine sensing among all synthesized heterojunctions. The detection mechanism was also discussed in detail. The in-built metal redox i.e Zn2+/Zn+ and Fe3+/Fe2+ facilitate the Z-scheme transfer, improve the charge transfer capacity and reduce the recombination. This study is beneficial because it reports utilization of popular and well-tested semiconductor metal oxides to form heterojunctions with dual capabilities of environmental detoxification and cost-effective electrochemical detection of biomolecules.

Utilization of Ag2O-Al2O3-ZrO2 decorated onto rGO as adsorbent for the removal of Congo red from aqueous solution.

The water resources contamination in an alarming concern for sustainable environment. This has led to development of new technologies and materials for waste water detoxification. In the present study, we have fabricated novel trimetallic based mixed oxides decorated reduced graphene oxide (rGO) composite using facile microwave method and utilized it as an adsorbent for the removal of congo red dye from aqueous solution. The final composite showed highly agglomerated metal oxides present on the rGO surface. The high surface area and activity of the synthesized adsorbent resulted in its high adsorption capacity of 333.32 mg/g for congo red. The Langmuir model better explained the isotherm data indicating the monolayer adsorption of congo red molecules onto Ag2O-Al2O3-ZrO2/rGO surface. The grander adsorption ability of Ag2O-Al2O3-ZrO2/rGO towards organic dye indicate its probable utilization in the removal of other dyes also from wastewater.

Contrasting effects of biochar and hydrothermally treated coal gangue on leachability, bioavailability, speciation and accumulation of heavy metals by rapeseed in copper mine tailings.

The purpose of this research was to examine the influence of hydrothermally treated coal gangue (HTCG) with and without biochar (BC) on the leaching, bioavailability, and redistribution of chemical fractions of heavy metals (HMs) in copper mine tailing (Cu-MT). An increase in pH, water holding capacity (WHC) and soil organic carbon (SOC) were observed due to the addition of BC in combination with raw coal gangue (RCG) and HTCG. A high Cu and other HMs concentration in pore water (PW) and amended Cu-MT were reduced by the combination of BC with RCG and/or HTCG, whereas individual application of RCG slightly increased the Cu, Cd, and Zn leaching and bioavailability, compared to the unamended Cu-MT. Sequential extractions results showed a reduction in the exchangeable fraction of Cu, Cd, Pb, and Zn and elevation in the residual fraction following the addition of BC-2% and BC-HTCG. However, individual application of RCG slightly increased the Cu, Cd, and Zn exchangeable fractions assessed by chemical extraction method. Rapeseed was grown for the following 45 days during which physiological parameters, metal uptake transfer rate (TR), bioconcentration factor (BCF), and translocation factor (TF) were measured after harvesting. In the case of plant biomass, no significant difference between applied amendments was observed for the fresh biomass (FBM) and dry biomass (DBM) of shoots and roots of rapeseed. However, BC-2% and BC-HTCG presented the lowest HMs uptake, TR, BCF (BCFroot and BCFshoot), and TF for Cu, Cd, Cr, Ni, Pb, and Zn in rapeseed among the other amendments compared to the unamended Cu-MT. Overall, these findings are indicative that using biochar in combination with RCG and/or HTCG led to a larger reduction in HMs leaching and bioavailability, due to their higher sorption capacity and could be a suitable remediation strategy for heavy metals in a Cu-MT.

Synthesis of composite sorbent for the treatment of aqueous solutions contaminated with methylene blue dye.

To apply the principles of sustainability, this study aims to prepare the composite sorbent from mixing of solid wastes that resulted from activities of treatment plants for wastewater and water supply. The manufacturing process depends on the mixing of sewage sludge with waterworks sludge at different proportions and the best mixture is modified by ferric nitrate solution. The prepared composite sorbent was evaluated as permeable reactive barrier (PRB) in the capturing of methylene blue (MB) dye presented in the simulated groundwater. Results proved that the suitable mixture of composite sorbent consisting of 0.25 g sewage sludge with 0.75 g waterworks sludge coated with aqueous solution of 2 g of Fe(NO3)2 achieved the maximum sorption capacity. In comparison with Freundlich model, Langmuir expression described the sorption measurements in a well manner; so, the chemisorption is governed by the removal of MB with maximum adsorption capacity reached to 268.98 mg/g. Kinetic measurements could be more representative by pseudo-first-order model and this means that the sorption process is supported by physical forces. Finally, the effects of inlet concentrations and bed thickness on the migration of MB front were simulated in an efficient manner by COMSOL Multiphysics 3.5a package with root mean squared errors not in excess of 0.152.

Mesoporous PtCu Alloy Nanoparticles with Tunable Compositions and Particles Sizes Using Diblock Copolymer Micelle Templates.

A simple, scalable route for the generation of mesoporous Rh particles by chemical reduction on self-assembled block-copolymer micelle templates was reported recently (Nat. Commun. 2017, 8, 15581). Here, this concept is extended to generate mesoporous PtCu alloy nanoparticles through the same approach. The PtCu alloy particles possess high-surface-area nanoporous architectures and good chemical stability for applications in catalysis. Both the composition and diameter of the bimetallic PtCu nanoparticles can be controlled by adjusting the amount of precursor in the reaction, which affects the electrochemical properties of the material. The combination of the mesoporous structure with the synergistic bimetallic electronic effects of PtCu gives rise to enhanced activity for the catalytic oxidation of methanol compared with commercial Pt black.

Visible photodegradation of ibuprofen and 2,4-D in simulated waste water using sustainable metal free-hybrids based on carbon nitride and biochar.

Rational designing of metal-free carbon nitride based photocatalysts can lead to an excellent optical response and a higher photocatalytic activity driven by visible and solar light. This combines green photocatalytic technology with greener materials prepared by facile approaches for environmental remediation. Herein we report utilization of star photocatalyst g-C3N4 (CN) to form highly efficient hetero-assemblies along with acidified g-C3N4 (ACN), polyaniline (PANI), reduced graphene oxide (RGO) and biochar. By use of these organic semiconductors we synthesize g-C3N4/ACN/RGO@Biochar (GARB), g-C3N4/PANI/RGO@Biochar (GPRB) and ACN/PANI/RGO@Biochar (APRB) nano-assemblies with different optical response and band edge positions for a better charge flow and reduced recombination of carriers. These synthesized catalysts were used for visible light powered degradation of 2,4-Dichlorophenoxy acetic acid (2,4-D) and ibuprofen (IBN). APRB performs the best and degrades 99.7% and 98.4% of 2,4-D and IBN (20 mg L-1) under Xe lamp exposure in 50 min and retention of high activity in natural sunlight. Optical analysis, photoelectrochemical response and radical quenching studies show both hydroxyl and superoxide radical anions as major reactive species and a Z-scheme photocatalytic mechanism. RGO acts as an electron mediator and protects higher positioned bands of PANI and ACN in APRB for a remarkable photocatalytic activity for a metal free material. The degradation pathway was analyzed by LC-MS analysis and 42% and 40% total organic carbon was removed in 2 h for 2,4-D and IBN degradation respectively. The toxicity of degraded products was analyzed by analyzing viability of human peripheral blood cells with retaining of 99.1% cells.

Adsorptive performance of MOF nanocomposite for methylene blue and malachite green dyes: Kinetics, isotherm and mechanism.

In the present study, Fe3O4@AMCA-MIL-53(Al) nanocomposite was utilized for the adsorptive removal of highly toxic MB and MG dyes from aqueous environment. The batch adsorption tests were performed at different contact time, pH, Fe3O4@AMCA-MIL-53(Al) dose, initial concentration of dyes and temperature. The maximum adsorption capacity of MB and MG dyes onto of Fe3O4@AMCA-MIL-53(Al) using Langmuir equation was 1.02 and 0.90 m mol/g, respectively. The isotherm and kinetic studies revealed that adsorption data were well fitted to Langmuir isotherm and pseudo-first-order kinetics models. Various thermodynamic parameters were also calculated and interpreted. The positive and negative values of ΔH° and ΔG° indicated that the adsorption was endothermic and spontaneous, respectively. The adsorptive binding of MB and MG on Fe3O4@AMCA-MIL53(Al) nanocomposite was directed by carboxylate and amide groups through electrostatic interaction, π-π interaction and hydrogen bonding. The desorption of both dyes from Fe3O4@AMCA-MIL-53(Al) was also performed using mixed solution of 0.01 M HCl/ethanol. Thus, we conclude that the Fe3O4@AMCA-MIL-53(Al) was an outstanding material for the removal of dyes from aqueous environment.