Porous TiO2/activated carbon (AC) material was synthesized by grafting peroxo-hydro titanium complexes to rice husk-derived activated carbon. It was found that the morphology of TiO2/AC consists of TiO2 fine particles highly dispersed on the AC matrix. The obtained TiO2/AC composites with high surface area and a red shift exhibit an excellent adsorption performance in both single and trinary system toward methylene blue (MB), methyl orange (MO), and methyl red (MR). The isotherm models including extended Langmuir, P-factor, ideal adsorbed solution theory (IAST) for Langmuir, Freundlich, and Sips models were applied to study the adsorption equilibrium data of trinary solutions. It was found that IAST for Freundlich and Langmuir models were the most suitable one to describe the adsorption of the three dyes on TiO2/AC material. The high maximum adsorption capacities (mmol g-1) in single/trinary mixture were found as 0.452/0.340 for MB; 0.329/0.321 for MO; and 0.806/2.04 for MR. Moreover, the recyclability experiments showed that the adsorbent could be reused through photocatalytic self-cleaning for at least three cycles with stable capacity. Thus, the TiO2/AC can be effectively employed for the removal of dyes from industrial textile wastewater.

Nano-zero-valent iron (nZVI) can be used to remove nitrate nitrogen (NO3-N) from groundwater. However, it has low reduction efficiency owing to its oxidation and aggregation characteristics. Thus, nZVI-loaded material is used to alleviate these drawbacks. In this study, nZVI-coated attapulgite (ATP) was prepared for the removal of NO3-N from groundwater. ATP-nZVI was prepared using the chemical liquid deposition-coreduction method. The prepared materials were characterized by SEM, XRD, and XPS analyses, which confirmed that the aluminum silicate particles in the ATP structure are effective carriers of nZVI and effectively inhibit self-consumption caused by the oxidation and aggregation of nZVI. The batch experiments examined experimental samples containing 30 mg/L nitrate and analyzed the effects of various parameters, including the material, mass ratio, initial pH, initial temperature, and coexisting anions on the NO3-N removal efficiency. The results showed that the optimal removal rate of the composite was 78.61%, which is higher than that using the same amount of ATP, iron powder, and nZVI. When the mass ratio of ATP to nZVI was 1 : 1, the NO3-N removal efficiency was the highest. When the pH value increased from 3 to 9, the NO3-N removal rate decreased, while an increase in the reaction temperature promoted NO3-N removal. The order of the inhibitory effect of coexisting anions on NO3-N removal by various nanoions was PO43–>CO32–>SO42–>Cl–. The adsorption kinetic model fitting results indicated that the chemisorption of electron exchange between ATP and nZVI in NO3-N removal was the main rate-limiting step in the reaction. This study demonstrates the potential of the prepared ATP-nZVI composite for NO3-N removal from groundwater.

Herein this study, pure and manganese- (Mn-) doped ZnO (2 wt. %) nanoparticles have been synthesized using the chemical precipitation method and characterized for the photodegradation of methyl green (MG) pollutant dye under natural sunlight. The structural analysis via XRD patterns has revealed that both intrinsic and Mn-doped ZnO (2 wt. %) samples have hexagonal wurtzite structures with appropriate phase purity, clearly indicating the absence of any external impurity. The incorporation of Mn in the host ZnO lattice has decreased the crystallite size (21.10 → 18.76 nm), and nanoparticle-type surface features with sizes in the 50–100 nm range have been observed through FESEM-based surface morphological studies. Both aforementioned observations have merit in providing more active area and a high surface area to volume ratio for photocatalytic reaction. The investigation of photophysical properties indicates that in Mn-doped ZnO nanoparticles, the absorption peak is blue-shifted by 5 nm (365 → 360 nm), due to the widening of the bandgap. The degradation kinetics of MG dye follow the pseudo-second-order kinetics, and the degradation efficiency has been observed to be 62.78% mediated by pure ZnO and 66.44% by Mn-doped ZnO (2 wt. %) photocatalyst under 60 minutes of sunlight irradiation. Specifically, the rate of photocatalytic reaction (K) ~0.01792 min-1 and ~0.97992 has been achieved for pure ZnO, whereas slightly higher (K) ~0.02072 min-1 and ~0.97299 have been observed for Mn-doped ZnO, respectively. Conclusively, the synergistic interactions with multiple charge transfer pathways, improvement of e−/h+ pair charge separation, improved surface area, and efficient generation of hydroxyl radicals are supposed to be responsible for the highly efficient photocatalytic activity of the Mn–doped ZnO photocatalyst for MG dye.

In order to simulate and calculate the leaching process of ionic rare earths more realistically, a digital model of ionic rare earths with real size, shape, seepage channel, and pore ratio and distribution at the mesoscopic scale was constructed based on nuclear magnetic resonance imaging (NMRI) technology. And the in situ leaching mining process was simulated and calculated by using three control equations of solution seepage, ion exchange, and solute migration. The reliability of the NMRI model was verified by the results of the indoor column leaching experiment, and the influence of the injection intensity and leaching agent concentration on the leaching of rare earth ions was analyzed. The results show that there are dominant seepage channels in the ore body, and the rare earth ion exchange reaction and migration in the dominant channel area are completed first. By analyzing the leaching results of rare earth ions under the working conditions of different injection strengths and different concentrations of leaching agent, the results show that the injection strength and the concentration of leaching agent have an obvious promoting effect on the leaching of rare earth ions in a certain range. The injection strength of 0.5~1.0 mL/min and the concentration of 0.20~0.25 mol/L leaching agent are considered to be more economical in practical engineering.

SF6/N2 gas mixture decomposition components can reflect the operation status inside GIS, and be used for fault diagnosis and monitoring inside GIS. NF3 and N2O are the characteristic decomposition components of SF6/N2 mixed gas. In order to find a potential gas sensitivity material for the detection of NF3 and N2O. This paper investigated the adsorption properties of NF3 and N2O on Al- and Ga- doped graphene monolayers based on density functional theory. Through the analysis of adsorption distance, charge transfer, adsorption energy, energy band structure, etc., the results indicated that the adsorption effect of Al- and Ga-doped graphene to NF3 and N2O are probably good, and these nanomaterials are potential to apply for the monitoring of GIS internal faults.

In this work, biochar produced from breadfruit leaves was utilized to remove the toxic Congo red dye. XRD, FTIR, and FESEM-EDX were implemented to characterize the biochar. Response surface methodology (RSM) and the Box-Behnken design (BBD) techniques were used to evaluate Congo red’s optimum adsorption efficiency. The adsorption of Congo red was studied by varying dye concentrations (5–50 mg/L), times (30–240 min), pH (6–9), and dosages (0.5–2 g/100 mL). X-ray diffractometer results show that the structure of biochar is amorphous. The biochar exhibited unbounded OH, aliphatic CH group, and C=O stretch, as shown by the band peaks at 3340 cm−1, 2924 cm−1, and 1625 cm−1 intensities. RSM-BBD design results showed maximum removal efficiency of 99.96% for Congo red at pH 6.37, dye concentration 45 mg/L, time 105 min, and dosage 1.92 g, respectively. The adsorption of Congo red by biochar was successfully modeled using the Langmuir model and pseudo-second-order model. The biochar produced from breadfruit leaves exhibited a high adsorption capacity of 17.81 mg/g for Congo red adsorption. It suggests that the adsorption is both homogenous monolayer and physicochemical.

The presence of heavy metals in wastewater, such as Ni, Pb, Cd, V, Cr, and Cu, is a serious environmental problem. This kind of inorganic pollutant is not biodegradable for several years, and its harmful effect is cumulative. Recently, semiconductor nanomaterials based on metal oxides have gained interest due to their efficiency in the removal of heavy metals from contaminated water, by inducing photocatalytic ion reduction when they absorb light of the appropriate wavelength. The most commonly applied semiconductor oxides for these purposes are titanium oxide (TiO2), zinc oxide (ZnO), and binary nanomaterials composed of both types of oxides. The main purpose of this work is to critically analyse the existent literature concerning this topic focusing specially in the most important factors affecting the adsorption or photocatalytic capacities of this type of nanomaterials. In particular, photocatalytic activity is altered by various factors, such as proportion of polymorphs, synthesis method, surface area, concentration of defects and particle size, among others. After a survey of the actual literature, it was found that, although these metal oxides have low absorption capacity for visible light, it is possible to obtain an acceptable heavy metal reduction performance by sensitization with dyes, doping with metallic or nonmetallic atoms, introduction of defects, or the coupling of two or more semiconductors.

The disposal of biological waste into water bodies is a major global concern as it leads to water pollution resulting in the loss of plenty of revenue in the cleaning of water bodies. Here, in the present research work, sacred flowers were collected, segregated, sun-dried, and powdered. The dried floral powders (marigold and rose) were characterized by field emission scanning electron microscopy (FESEM), electron diffraction spectroscopy (EDS), Fourier transforms infrared spectroscopy (FT-IR), and X-ray diffraction (XRD). The microscopy revealed the irregular spherical shape of the sheet-like structure whose size varies in microns. The EDS revealed the elemental composition which was dominated by mainly carbon and oxygen. The XRD shows the presence of carbon (10-25ɵ) in the amorphous form and the absence of any crystalline phase in the biosorbents. The FT-IR showed peaks that conformed to the presence of functional groups like -OH and a carbonyl group. The dried powders were used as an economical and eco-friendly biosorbent for the removal of methyl red (MR) dye from the aqueous solutions by batch adsorption study. After 60 minutes of contact time, the marigold powder (MGP) and rose petal powder (RPP) showed decolorization of 61.16% and 56.08% for 2 ppm of MR dye. The kinetic revealed that the dye removal reaction does not follow the pseudo-first-order as well as the pseudo-second-order. The utilization of such waste-based biosorbents will minimize solid waste and also will provide an economical biosorbent for the removal of environmental pollutants.

Methylene blue dye (MB dye) is a harmful contaminant for wastewater streams of industries and is harmful to human and aquatic life. An ecofriendly sugar templating process was used to generate porous bentonite/polydimethylsiloxane (PB) and porous magnetite nanoparticles/bentonite/polydimethylsiloxane (PBNP) composite absorbents to remove MB dye in this study. During the infiltration of PDMS solution into the sugar template in the vacuum chamber, bentonite and magnetite particles were integrated on the surface of the PDMS, and the porous structure was generated during the leaching out of sugar particles in water. The absorbents were characterized using Fourier infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The absence of the methyl bond at 2924 cm-1 and phenol bond at 3325 cm-1 in the FTIR spectra of the formed membrane proves that the food grade sugar was completely removed. The SEM images confirm that porosity was achieved as well as uniform mixing of the in the formation of composite. MB dye was effectively removed from wastewater using the as-prepared composite as absorbent. The removal efficiencies of the composite PBNP and PB were ~91% and ~85%, respectively. The experimental data was applied to pseudo-first-order (PFO) and pseudo-second-order (PSO) kinetic models as well as the Dubinin-Radushkevich, Harkins-Jura, and Elovich models for the adsorption isotherm. The data was found to fit the pseudo-second-order and Elovich models, respectively. The results show that the presence of magnetite nanoparticles improved MB dye removal significantly.

Thermoplastic-based polymers are gathering importance in several engineering fields like electrical, electronic, automotive, aerospace, and structural. The additions of secondary phase reinforcements such as natural and synthetic fibre improve thermoplastic-based polymer’s properties. The thermoplastic and natural fibre combinations are found to have low mechanical strength and incompatibility and need special treatment for synthesizing the natural fibre. The present experimental investigation deals with the enhancement of polypropylene hybrid composite by using the combinations of glass (synthetic)/hemp (natural) fibre for the ratio of 0 : 35, 5 : 30, 10 : 25, and 15 : 20 reinforced with 5 wt% compatibilizer through injection moulding. The revealed test results of polypropylene hybrid composite showed improved mechanical impact and flexural and tensile strength of 37.5%, 14.2%, and 21.1%, respectively. The thermal adsorption characteristics were evaluated by thermogravimetric analysis apparatus. It showed the decomposition of composite limited by hemp fibre at 27°C to 700°C.

In this work, a new adsorbent with effective Pd(II) adsorption ability was synthesized using an oyster shell and fumed silica as the matrix materials and polyethyleneimine as the functional ligand. The adsorption performance of the developed adsorbent was evaluated for the recovery of palladium chloride ions (Pd(II)) from strong acid solutions. To understand the characteristics of the materials used in the study, samples were characterized by Fourier transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), X-ray diffraction (XRD), and zeta potential analysis. Zeta potential analysis revealed that the isoelectric point of polyethylenimine-crosslinked calcium silicate hydrate (PEI-CSH) was 9.85. Isotherm experiments revealed that the maximum Pd(II) uptake estimated by the Langmuir model was 156.03 mg/g, which was 22.4 and 35.6 times higher than that of the oyster shell powder (OSP) and calcium silicate hydrate (CSH), respectively. The Pd(II) adsorption equilibrium was established in 180 minutes, according to kinetic experiments. These results suggested the possibility of Pd(II) recovery from oyster shell-based adsorbent. Through five adsorption and desorption cycles, the reusability of PEI-CSH was confirmed. PEI-CSH can therefore be considered a potential adsorbent for Pd(II) recovery.

“Aged refuse” corresponds to municipal solid waste material dumped in land, for several years. This solid waste material is chosen as an adsorbent for the current study since it is available abundantly in the state of Tamil Nadu, India, and has not been used for any other applications. The current study was conducted to get rid of the element chromium (VI) from wastewater by using the adsorption process. The aged refuse was analytically tested through various processes such as BET, TGA, XRD, SEM, and FTIR to determine the surface morphology, functional groups, thermal stability, nature of the crystalline, and surface area. The researchers conducted the batch adsorption study to validate the influence exerted by different sorts of adsorption parameters like contact time (10-100 min), initial concentration of the pollutant (50 mg·L-1 to 250 mg·L-1), pH (1-7), and the dosage of the adsorbent (0.5 g·L-1-3.0 g·L-1). In the current study, the researchers achieved the maximum adsorption capacity of 195.54 mg·g-1. From the kinetic results, it can be understood that the pseudo-first-order model was the most suitable kinetic model. Further, the study outcomes confirm that the Langmuir isotherm model is the best fit by isotherm studies which indicate the monolayer adsorption process. This study indicated that the aged refuse can be potentially used in removing Cr (VI) from water environment under standard optimized conditions.

In the present investigation, zinc oxide nanorods (ZnO-NR) were synthesized via the hydrothermal method using ZnCl2 as a zinc ion precursor in the presence of cetyltrimethylammonium bromide. Synthesized ZnO-NR was featured using advanced techniques including XRD, PL, SEM, and UV-visible spectroscopy. The role of these assynthesized ZnO-NR was evaluated for the sequestration of lead ions in batch mode. The elimination of lead ions was achieved at pH 6-7 using a 0.06 g adsorbent dose, 25 min contact time, 25 mg/L initial lead ion concentration, 323 K temperature, and 200 rpm agitation speed. A thermodynamic study revealed the endothermic nature of lead ion sequestration onto ZnO-NR. The lead ion sequestration followed kinetic (pseudo-second-order) and isotherm (Langmuir) models. The lead ions were eliminated up to 142 mg/g at the optimum level of affecting variables. The ZnO-NR might be a potential adsorbent for lead ion removal from industrial effluents.

Due to the excessive use of paracetamol (PCM), a significant amount of its metabolite has been released into the surroundings, and its removal from the surroundings must happen quickly and sustainably. Multicomponent adsorption modelling is difficult because it is challenging to anticipate the relationships among the adsorbates in this artificial intelligence-based modelling, a choice among different algorithms. Utilizing various algorithms, many studies assessed the single and binary adsorption of paracetamol on activated carbon. The present study implements that the effectiveness of PCM adsorption on a carbon-activated nanomaterial was predicted using an artificial neural network, a machine learning technology. As a factor of adsorbent particle size, adsorbent dosage, training time, and starting concentrations, the adsorption capacity for each medicinal ingredient was examined. SEM was used to analyze a nanomaterial that had been chemically altered with orthophosphoric acid (FTIR). To determine the residual proportion of PCM in solvent, batch adsorption of PCM was then carried out at various operation conditions, including contact time, temperatures, and initial dosage. The adsorption effectiveness of paracetamol on carbon-activated nanoparticle was calculated using experimental results. Thus, by using machine learning framework, the adsorption efficiency of paracetamol on a carbon-activated nanomaterial was predicted.

Novel constitutions of ceramic bond the new opportunity of engineering materials via solid-state process attaining enhanced material characteristics to overcome the drawback of conventional materials used in aquatic applications. The copper-based materials have great potential to explore high corrosion resistance and good thermal performance in the above applications. The main objectives of this research are to develop and enhance the characteristics of the copper-based hybrid nanocomposite containing different weight percentages of alumina and graphite hard ceramics synthesized via solid-state processing (powder metallurgy). The presence of alumina nanoparticles with a good blending process has to improve the corrosion resistance, and graphite nanoparticles may limit the weight loss of the sample during potentiodynamic corrosion analysis. The developed composite’s micro Vickers hardness is evaluated by the E384 standard on ASTM value of 69 Hv and is noted by increasing the weight percentages of alumina nanoparticles. The conduction temperature of actual sintering anticipates the thermogravimetric analysis of developed composite samples varied from 400°C to 750°C. The thermogravimetric graph illustration curve of the tested sample found double-step decomposition identified between 427°C and 456°C. The potentiodynamic analyzer is used to evaluate the corrosion behaviour of the sample and the weight loss equation adopted for finding the theoretical weight loss of the composite.

This study is aimed at extending the soybean hulls’ lifetime by their utilization as an adsorbent for metal ions (Cd2+ and Cu2+) and dyes (Reactive Yellow 39 (RY 39) and Acid Blue 225 (AB 225)). ATR-FTIR spectroscopy, FE-SEM microscopy, and zeta potential measurements were used for adsorbent characterization. The effect of the solution’s pH, peroxidase extraction, adsorbent particle size, contact time, the pollutant’s initial concentration, and temperature on the soybean hulls’ adsorption potential was studied. Before peroxidase extraction, soybean hulls were capable of removing 72% Cd2+, 71% Cu2+ (at a pH of 5.00) or 81% RY 39, and 73% AB 225 (at a pH of 3.00). For further experiments, soybean hulls without peroxidase were used for several reasons: (1) due to their observed higher metal ion removal, (2) in order to reduce the waste disposal cost after the peroxidase (usually used for wastewater decolorization) extraction, and (3) since the soybean hulls without peroxidase possessed significantly lower secondary pollution than those with peroxidase. Cd2+ and Cu2+ removal was slightly increased when the smaller adsorbent fraction (710-1000 μm) was used, while the adsorbent particle size did not have an impact on dye removal. After 30 min of contact time, 92% and 88% of RY 39 and AB 225 were removed, respectively, while after the same contact time, 80% and 69% of Cd2+ and Cu2+ were removed, respectively. Adsorption of all tested pollutants follows a pseudo-second-order reaction through the fast adsorption, intraparticle diffusion, and final equilibrium stage. The maximal adsorption capacities determined by the Langmuir model were 21.10, 20.54, 16.54, and 17.23 mg/g for Cd2+, Cu2+, RY 39, and AB 225, respectively. Calculated thermodynamic parameters suggested that the adsorption of all pollutants is spontaneous and of endothermic character. Moreover, different binary mixtures were prepared, and the competitive adsorptions revealed that the soybean hulls are the most efficient adsorbent for the mixture of AB 225 and Cu2+. The findings of this study contribute to the soybean hulls’ recovery after the peroxidase extraction and bring them into the circular economy concept.

The pollution due to dyes from textile sector is one of the major issues faced worldwide. This study was focused on the removal of the reactive dye, Drimaren Turquoise CL-B using Schizophyllum commune, a white rot fungus (WRF) keeping in mind the current environmental conditions. Different parameters like pH, sources of carbon & nitrogen, temperature, concentration of dye and C/N ratio were used to investigate their effect on the process. Maximum dye removal of 95.45% was obtained at pH 4.5, temperature 35°C, inoculum size 3 mL, veratryl alcohol (mediator), glucose (carbon source) and ammonium nitrate (nitrogen source). The enzyme activity was determined by employing enzyme assay. Laccase and Lignin peroxidase (LiP) activity was low while Manganese peroxidase (MnP) activity was highest. Maximum bio-sorption was achieved at pH 1 and 313 K. The pseudo-2nd-order kinetic model & Freundlich isotherm was best suited for the process of removal of dye. From these data, it is concluded that white rot fungus could possibly be the excellent biomaterial for elimination of synthetic dyes from wastewater.

p-sulphonated calix[4]arene (p-SOCX) functionalized cellulose acetate/graphene oxide (CA/GO) nanofibers were successfully prepared via the electrospinning technique. The presence of p-SOCX within the fiber matrix was ascertained using Fourier Transform Infrared spectroscopy and Carbon-Hydrogen-Nitrogen-Sulphur elemental analyses. Apparent changes in morphology of the samples were observed under scanning electron microscope where fiber diameters increased with increasing p-SOCX content. Preliminary dye removal test at different pH, dosage, and temperature of functionalized CA/GO nanofiber demonstrates enhanced adsorption capacity of methylene blue in presence of p-SOCX compared to pristine CA nanofiber and CA/GO nanofiber at an optimum pH 8. The highest removal efficiency obtained was 88.84% with initial methylene blue dye concentration of 10 mg/L, adsorbent dosage of 20 mg/10 mL, contact time of 30 min at room temperature ca. 293 K.

Emerging contaminants (ECs) are substances that have been detected in water but have not been thoroughly tested or regulated. Pesticides, cosmetics, pharmaceuticals, and other medications are examples of compounds in this category. Even at low quantities, these pollutants can harm human health and the environment; therefore, avoiding them is critical. The consequences of EC pollution on the endocrine, hormonal, and genetic systems are causing significant concern. Even with current best practices and available technology, it is difficult to totally eliminate ECs from municipal and industrial wastewater treatment plants. Adsorption has been the method of choice for EC removal since it is less costly, more effective, and easier to use. To treat ECs, newer generation nanoadsorbents are employed. Adsorption was greatly enhanced by functional changes to the adsorbent surface. Carbon nanostructures are widely used as adsorbents because of their outstanding surface properties, adaptability, large surface area, adjustable structural changes, and high chemical stability. This review reviews and examines recent research on the production and use of carbon-based nanoadsorbents. The emphasis is on carbon nanotubes, graphene, and graphene-derived adsorbents. It is being investigated if these adsorbents can be used to extract hormone-disrupting chemicals and other emerging pollutants. The sources and classification of these pollutants, treatment knowledge gaps, and novel prospects for increasing carbonaceous nanoadsorbent utilization were all explored. The environmental and health problems associated with EC use are also studied.

The sorption mechanisms, point of zero charge, and isosteric heats involved in the adsorptive dephenolization of aqueous solutions using thermally modified corn cob (TMCC) were studied at different initial phenol concentrations (100–500 mg/l), TMCC dosage (0.4–2.0 g), contact time (5–60 min), pH (2–10), and temperature (30–60°C). Analysis of the adsorbent material showed that it possessed the properties typical of a good adsorbent. The adsorption experiments revealed that phenol uptake is favored by an increase in TMCC dosage and contact time and a decrease in temperature and concentration of phenol in the solution. The experimental data were well-fitted to the Sips, Langmuir, Toth, and Redlich–Peterson isotherm models. Thermodynamic studies suggested that the sorption of phenol onto TMCC is feasible, spontaneous, and endothermic. The isosteric heats of adsorption obtained are in the range 47.43-79.38 kJ/mol, confirming that the adsorption process is predominantly a physical process depicting the van der Waals interactions, and it is inversely proportional to surface loading. The analysis of the adsorption mechanisms showed that the intraparticle, film, and pore diffusion mechanisms were significantly involved in the phenol adsorption process. The involvement of electrostatic attraction, electron-donor interaction, and hydrogen bonding was also demonstrated. The point of zero charge () was obtained at a pH of 5.83; being slightly lower than the optimum pH of 6 indicates that the sorbent surface is obviously not negatively charged at . The discoveries of this study have shown that the dephenolization process is feasible, spontaneous, endothermic, dominated by a physical process, and governed by intraparticle, film, and pore diffusion mechanisms.