Most laboratory studies have focused on the effects of nanoplastics instead of plastics at the micrometer scale, which are the major microplastics (MPs) discarded in marine environments. Knowledge on the potential effects of micrometer scale plastics on marine microalgae remains limited. It remains unknown whether the micrometer scale plastics also affect microalgal growth, lipid accumulation and resistance to organic contaminants? In addition, the role of polymer-size on the potential hazardous effects of MPs on microalgae is unknown. In the present study, cell populations of a marine diatom, Phaeodactylum tricornutum, were treated with micrometer scale polyethylene (PEMP, 150 μm) and unplasticized polyvinyl chloride (uPVCMP, 250 μm) powders in the laboratory. Growth was assessed using a hemacytometer and neutral lipid concentrations were evaluated using the Nile Red staining method under short-term (four days) and long-term (nine days) exposure. The effects of combined PEMP and phenanthrene (Phe), and uPVCMP and Phe exposures over four days on growth were investigated. Importance scores and SHapley Additive exPlanations (SHAP) values were calculated to assess the contributions of seven factors in exposure systems to the hazardous effects of MPs on microalgae using a machine-learning prediction based on 165 data sets. Both MP types did not influence algal growth and lipid accumulation but minimized algal inhibition by the action of Phe at four days. In addition, lipid accumulation was induced at nine days. Both importance scores and SHAP values indicated that MP polymer-size was the key factor influencing MP toxicity in microalgae. In conclusion, MPs had adverse effects only in chronic tests and the potential adsorption of MPs could have led to the lower levels of toxicity in a combined MP–Phe exposure system. Compared to nanoplastics, MPs in the hundred-micrometer range do not significantly affect growth and their adsorption would not be influenced by size. Therefore, MP size is the most critical factor that should be considered in future laboratory tests and eco-toxicological risk assessments for microalgae.

The N-TiO2/g-C3N4@diatomite (NTCD) composite has been prepared through a simple impregnation method, using titanium tetrachloride as precursor and urea as nitrogen-carbon source. Then the effects of calcination temperature on structure, surface property and photocatalytic activity of the catalysts were investigated. And XRD, TEM, XPS, FTIR and UV–vis diffuse adsorption spectroscopy were used to characterize the obtained powders. The photocatalytic activity of the NTCD was evaluated through the reduction of aqueous Cr (VI) under visible light irradiation (λ > 400 nm). The results demonstrated that the nano-TiO2 particles ranging from 15 to 30 nm in the crystal of anatase are well deposited on the surface of diatomite in the NTCD-500 which calcined at 500 °C for 2 h. Furthermore, the g-C3N4 with the lay thickness of 0.92 nm was attached to the surface of nano-TiO2. The N-doped TiO2 and g-C3N4 doped catalysts could co-enhance response in the visible light region and reduce band gap of NTCD-500 (Eg = 3.07 eV). And the NTCD-500 sample exhibited nearly 100% removal rate within 5 h for photocatalytic reduction of Cr (VI) which was higher activity than P25, crude TiO2@diatomite and g-C3N4@diatomite.

A comprehensive study of the removal of selected biologically active compounds (pharmaceuticals and pesticides) from different water types was conducted using bare TiO₂ nanoparticles and TiO₂/polyaniline (TP-50, TP-100, and TP-150) nanocomposite powders. In order to investigate how molecular structure of the substrate influences the rate of its removal, we compared degradation efficiency of the initial substrates and degree of mineralization for the active components of pharmaceuticals (propranolol, and amitriptyline) and pesticides (sulcotrione, and clomazone) in double distilled (DDW) and environmental waters. The results indicate that the efficiency of photocatalytic degradation of propranolol and amitriptyline was higher in environmental waters: rivers (Danube, Tisa, and Begej) and lakes (Moharač, and Sot) in comparison with DDW. On the contrary, degradation efficacy of sulcotrione and clomazone was lower in environmental waters. Further, of the all catalysts applied, bare TiO₂ and TP-100 were found to be most effective in the mineralization of propranolol and amitriptyline, respectively, while TP-150 appeared to be the most efficient in terms of sulcotrione and clomazone mineralization. Also, there was no significant toxicity observed after the irradiation of pharmaceuticals or pesticides solutions using appropriate catalysts on rat hepatoma (H-4-II-E), mouse neuroblastoma (Neuro-2a), human colon adenocarcinoma (HT-29), and human fetal lung (MRC-5) cell lines. Subsequently, detection and identification of the formed intermediates in the case of sulcotrione photocatalytic degradation using bare TiO₂ and TP-150 showed slightly different pathways of degradation. Furthermore, tentative pathways of sulcotrione photocatalytic degradation were proposed and discussed.

This paper investigated the application of graphite particle electrodes to the removal of Zn, Pb, Cu, and Cd from municipal solid waste incineration (MSWI) fly ashes in a three-dimensional (3D) electrokinetic reactor. The influences of the voltage gradient, mass ratio of graphite powers to fly ashes, nitric acid concentrations, proposing times, and liquid-solid (L-M) ratios on the remedial efficiencies of MSWI fly ashes were comprehensively studied in an orthogonal deign and a sequential double-factor setup. Significant analysis showed that changes in the mass ratios and nitric acid concentrations both had a statistically significant effect on the removals of Zn and Pb. Proposing times and L-M ratios both remarkably affected the removals of heavy metals (HMs) in a 3D electrochemical system. The graphite powers had a narrower distribution interval and slightly larger surface areas compared with MSWI fly ashes, which relented pH gradients over the time in the electrochemical experiments and minimized the bubble barricade caused by the hydrolysis. The particle electrode had increased the residue factions of Zn, Pb, Cu, and Cd in S1 region by approximately 216%, 136%, 309%, and 950%, respectively, compared with the raw MSWI fly ashes. The addition of graphite powders to a two-dimensional (2D) electrochemical process strengthened hydrolysis reactions, shortened time for the redistribution of pH balance, decreased the tortuosity of migration path, and increased the desorption concentrations of HMs in the sample area.

Carbon dioxide gas as a working gas produces a stable plasma-torch by making use of 2.45 GHz microwaves. The temperature of the torch flame is measured by making use of optical spectroscopy and a thermocouple device. Two distinctive regions are exhibited, a bright, whitish region of a high-temperature zone and a bluish, dimmer region of a relatively low-temperature zone. The bright, whitish region is a typical torch based on plasma species where an analytical investigation indicates dissociation of a substantial fraction of carbon dioxide molecules, forming carbon monoxides and oxygen atoms. The emission profiles of the oxygen atoms and the carbon monoxide molecules confirm the theoretical predictions of carbon dioxide disintegration in the torch. Various hydrocarbon materials may be introduced into the carbon dioxide torch, regenerating new resources and reducing carbon dioxide concentration in the torch. As an example, coal powders in the carbon dioxide torch are converted into carbon monoxide according to the reaction of CO2 + C → 2CO, reducing a substantial amount of carbon dioxide concentration in the torch. In this regards, the microwave plasma torch may be one of the best ways of converting the carbon dioxides into useful new materials.

Mg, Zn, Mn, and Al oxide powders have been synthesized through chemical combustion and calcination methods to compare their CO₂ capture performances. The characteristic properties of the adsorbents were evaluated by X-ray diffraction analysis, scanning electron microscopy, and N₂ physisorption measurements. The porous γ-Al₂O₃ prepared through combustion with a BET-specific surface area of 192.1 m²/g, achieving a maximum gas adsorption capacity of 1.71 mmol/g at 60 °C and 1.5 MPa. The MgO adsorbent performed poorly during CO₂ capture, while that Zn and Mn oxides showed no CO₂ adsorption. The results showed theoretical contribution to the field of separation science.

Batch sorption experiments were carried out to investigate the potentiality of papaya leaf powder (PLP) for the removal of methylene blue (MB) from aqueous solution. The effects of various experimental parameters, such as adsorbent dose, initial solution concentration, contact time, and solution pH were also studied. The amount of dye adsorbed was found to increase with increase in initial dye concentrations. Papaya leaf adsorbs MB better in basic medium. The adsorption equilibrium data fitted well in the Langmuir isotherm equation with a monolayer sorption capacity of 512.55 mg g⁻¹. The kinetics of MB adsorption onto papaya leaf was examined using the pseudo-first and pseudo-second order and unified approach kinetic models. The adsorption kinetics followed the pseudo-second order kinetic model, but the rate constant was found to depend on initial dye concentration. The unified approach model described the equilibrium and kinetics well. The forward and backward rate constants were determined from the unified approach model.

The adsorption of Cu(II) ions by sodium-hydroxide-treated Imperata cylindrica (SoHIC) leaf powder was investigated under batch mode. The influence of solution pH, adsorbent dosage, shaking rate, copper concentration, contact time, and temperature was studied. Copper adsorption was considered fast as the time to reach equilibrium was 40-90 min. Several kinetic models were applied and it was found that pseudo-second-order fitted well the adsorption data. In order to understand the mechanism of adsorption, spectroscopic analyses involving scanning electron microscope (SEM) coupled with energy-dispersive spectroscopy (EDS) and Fourier transform infrared (FTIR) spectrophotometer were carried out. Ion exchange was proven the main mechanism involved as indicated by EDS spectra and as there was a release of light metal ions (K⁺, Na⁺, Mg²⁺, and Ca²⁺) during copper adsorption. Complexation also occurred as demonstrated by FTIR spectra involving hydroxyl, carboxylate, phosphate, ether, and amino functional groups. The equilibrium data were correlated with Langmuir, Freundlich, and Dubinin-Radushkevich isotherm models. Based on Langmuir model, the maximum adsorption capacity was recorded at the highest temperature of 310 K, which was 11.64 mg g⁻¹.

This paper presents a study on the batch adsorption of a basic dye, methylene blue (MB), from aqueous solution onto ground hazelnut shell in order to explore its potential use as a low-cost adsorbent for wastewater dye removal. A contact time of 24 h was required to reach equilibrium. Batch adsorption studies were carried out by varying initial dye concentration, initial pH value (3-9), ionic strength (0.0-0.1 mol L⁻¹), particle size (0-200 μm) and temperature (25-55°C). The extent of the MB removal increased with increasing in the solution pH, ionic strength and temperature but decreased with increase in the particle size. The equilibrium data were analysed using the Langmuir and Freundlich isotherms. The characteristic parameters for each isotherm were determined. By considering the experimental results and adsorption models applied in this study, it can be concluded that equilibrium data were represented well by Langmuir isotherm equation. The maximum adsorption capacities for MB were 2.14 x 10⁻⁴, 2.17 x 10⁻⁴, 2.20 x 10⁻⁴ and 2.31 x 10⁻⁴ mol g⁻¹ at temperature of 25, 35, 45 and 55°C, respectively. Adsorption heat revealed that the adsorption of MB is endothermic in nature. The results indicated that the MB strongly interacts with the hazelnut shell powder.

Hydrothermal synthesis followed by a calcination step was used to prepare porous Zn₂SnO₄ powders using carbon black as a pore-forming agent. The porous Zn₂SnO₄ was used as a photocatalyst to degrade the Rhodamine B dye from aqueous solution under UV artificial light. X-ray diffraction, N₂ adsorption-desorption isotherms, and UV-Vis diffuse reflectance were used to characterize the material. The addition of pore-forming agent (carbon black) did not change the crystalline structure of Zn₂SnO₄ phase. In addition, increasing the surface area and porosity as well as decreasing the band-gap energy was observed. The combination of these characteristics favored the photodegradation of Rhodamine B, reaching 96% of dye degradation at 15 min of reaction time. In addition, the photocatalyst was active after six cycles of reuse. Therefore, the produced material in this work showed to be a potential photocatalyst to remove Rhodamine B dye from aqueous solution.