Catalytic pyrolysis is a promising chemical recycling technology to supplement mechanical recycling since plastics can be broken down into monomers or converted to the required fuels and chemicals. In this study, a microwave (MW) -responsive SiC foam@zeoltie core-shell structured catalyst was proposed for the catalytic pyrolysis of polyolefins. Under microwave irradiation, the SiC foam core works as both microwave adsorber and catalyst support, thus concentrating the generated heat energy on the ZSM-5 zeolite shell, where the catalytic reaction takes place. SiC foam with an open cellular structure can also improve the global transport of mass and heat during plastics pyrolysis. In this work, the effects of the SiO₂/Al₂O₃ ratio and alkaline treatment of ZSM-5 zeolite coated SiC foam under MW irradiation on the variations in product distribution from low-density polyethylene (LDPE) pyrolysis were investigated at 450 °C. The results indicated that the appropriate acidity and pore structure were crucial to upgrading gas and liquid products. Particularly, the creation of a mesoporous structure in ZSM-5 zeolite via alkaline treatment could improve the diffusion of large molecules and products, thus significantly increasing the selectivity of high-valued light olefins and aromatics while inhibiting the formation of unwanted alkanes, which are expected in the chemical industry. Concretely, the concentration of olefins in gas increased to 51.0 vol% for ZSM-5(50)-0.25AT, and 65.6 vol% for ZSM-5 (50)-0.50AT, compared with 45.2 vol% for the parent ZSM-5(50). The relative concentration of aromatics in liquid decreased from 96.6% for ZSM-5(50) to 75.9% for ZSM-5(50)-0.25AT, and 71.1% for ZSM-5(50)-0.50AT. Given the respective yield of gas and liquid, the total selectivity of C2–C4 olefins and aromatics for mesoporous ZSM-5 zeolites could reach 58.6–64.9% during LDPE pyrolysis, which were higher than that for the parent ZSM-5 zeolite.

Microwave irradiation (MW) is an effective technique in heating and pyrolysis. This study compared the properties of peanut shell-biochars produced using MW and muffle furnace (FN). At the same pyrolysis temperature, MW biochars preserved more biomass (as indicated by their higher yields and higher abundance of functional groups) and possessed larger surface areas due to the high abundance of micropores. MW biochars generally exhibited higher adsorption of carbamazepine (CBZ) and bisphenol A (BPA) than FN biochars. However, their surface area-normalized sorption was lower, suggesting that the inner pores may not be fully available to CBZ and BPA sorption. We observed significant free radical signals in both types of biochars. Although CBZ and BPA did not degrade in the biochar sorption systems, the potential role of stronger free radical signals in MW biochars for organic contaminant control may not be overlooked in studies with other chemicals.

The present work reports microwave-assisted synthesis of SnO₂ nanoparticles via green route using Psidium Guajava extract. For the enhancement of catalytic activity, nanohybrids of SnO₂ were formulated using different ratios of polyaniline (PANI) via ultrasound-assisted chemical polymerization. Formation of nanohybrids was confirmed via IR and XPS studies. The UV–vis DRS spectra of PANI/SnO₂ revealed significant reduction in the optical band gap upon nanohybrid formation. Microwave-assisted catalytic efficiency of pure SnO₂, PANI, PANI/SnO₂ nanohybrids was investigated using DDT as a model persistent organic pollutant. The degradation efficiency of PANI/SnO₂ was found to increase with the increase in the loading of PANI. Around 87% of DDT degradation was achieved within a very short period of 12 min under microwave irradiation using PANI/SnO₂-50/50 as catalyst. The effect of DDT concentration was explored and the degradation efficiency of PANI/SnO₂-50/50 catalyst was noticed to be as high as 82% in presence of 100 mg/L of DDT. The effect of microwave power on the degradation efficiency revealed 79% degradation using the same nanohybrid when exposed to microwave irradiation for 5 min under 1110 W microwave power. Scavenging studies confirmed the generation of OH, O₂⁻ radicals. The fragments with m/z values as low as 86 and 70 were confirmed by LCMS analysis. Recyclability tests showed that PANI/SnO₂-50/50 nanohybrid exhibited 81% degradation of DDT (500 mg/L) even after the third cycle, which reflected high catalytic efficiency as well as remarkable stability of the catalyst. This green nanohybrid could therefore be effectively utilized for the rapid degradation of persistent organic pollutants.

Spiramycin is a widely used macrolide antibiotic and exists at high concentration in production wastewater. A thermal-acid hydrolytic pretreatment using silicotungstic acid (STA) under microwave (MW) irradiation was suggested to mitigate spiramycin from production wastewater. Positive correlations were observed between STA dosage, MW power, interaction time and the hydrolytic removal efficiencies, and an integrative equation was generalized quantitively. Rapid and complete removal 100 mg/L of spiramycin was achieved after 8 min of reaction with 1.0 g/L of STA under 200 W of MW irradiation, comparing to 30.1% by MW irradiation or 15.9% by STA alone. The synergetic effects of STA and MW irradiation were originated from the dissociated-proton catalysis by STA and the dipolar rotation heating effect of MW. STA performed much better than the mineral acid H2SO4 under MW, due to the much stronger Brönsted acidity and higher Hammett acidity. After 8 min, 98.0% of antibacterial potency was also reduced. The m/z 558.8614 fragment (P1) and m/z 448.1323 fragment (P2) were identified as the primary products, which were formed by breaking glucosidic bonds and losing mycarose and forosamine for P1 and further mycaminose moiety for P2. Finally, production wastewater with 433 mg/L of spiramycin was effectively treated using this thermal-acid hydrolytic method. Spiramycin and its antibacterial potency both dropped to 0 after 6 min. The potency drop was supposed from the losing of mycarose and/or forosamine. To decrease both the concentration of spiramycin and its antibacterial potency, combinedly using STA and MW was suggested in this work to break down the structural bonds of the functional groups rather than to destroy the whole antibiotic molecules. It is promising for pretreating spiramycin-contained production wastewater to mitigate both the antibiotic and its antibacterial potency.

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.

A green and-easy to operate method, the microwave technology, was developed to promote the desulfurization process of phosphate rock, systematically investigates the strengthening effect of microwave, and uses XRD, BET, SEM, XRF, ICP, and EDS to characterize the reactants. The results show that the main reason for the desulfurization efficiency is improved by microwave heating under microwave conditions, different thermal stress phosphate rock materials lead to the destruction of each microstructure, and a specific surface area increased 40.25% phosphate rock. In addition, after microwave irradiation, the pore size of the phosphate rock at 2–5 nm is significantly increased, and the number of mesopores is significantly increased, thereby increasing the desulfurization efficiency of the phosphate rock. By investigating the effects of temperature, oxygen content, flow rate, and solid-liquid ratio on desulfurization efficiency, the paper concludes that the optimal conditions for desulfurization of phosphate rock after microwave irradiation are C(SO₂) is 2500 mg·m⁻³, temperature is 40 °C, φ(O₂) is 5%, solid-liquid ratio is 3.5 g:200 ml, and flue gas flow is 500 ml·min⁻¹.

Microwave-assisted catalytic oxidation technology has become an effective technology for rapid removal of organic pollutants in wastewater. In this research, the removal of methyl orange (MO) from aqueous solution by CuFe₂O₄ loaded on carbon nanotubes (CuFe₂O₄/CNTs) under microwave irradiation was studied. The effects of different loadings (1:2, 1:4, 1:8) of CuFe₂O₄ on the dielectric loss, magnetic loss, dielectric loss factor, magnetic loss factor, and reflection loss of composite materials were studied. The results showed that the microwave adsorption performance was improved by loading CuFe₂O₄ on CNTs. These different composites were further characterized by SEM, FTIR, and XRD techniques. In addition, this article also studied the effects of different microwave irradiation time, pH, and ionic factors on the degradation of MO. In particular, the mechanism of MO degradation by composite materials under different pH conditions was also studied in detail. The results showed that the removal rate reaches 97% with 5 min under the best conditions, and the composite material had good anti-interference performance. This study may provide a new option to degrade organic dye in wastewater treating.

The present work describes the synthesis of α-MnO₂ nanorods using a natural extract of Brassica oleracea (cabbage) and the formulation of its nanohybrids with polycarbazole, i.e., α-MnO₂/PCz. Synergistic interaction between PCz and MnO₂ is revealed from infrared spectroscopy (IR) studies while the composition is determined by X-ray photoelectron spectroscopy (XPS). The formation of α-MnO₂ nanorods is confirmed via high-resolution transmission electron microscopy (HRTEM). The indirect bandgap of α-MnO₂ is reported as 2.5 eV while for the nanohybrids it is found to be ranging between 2.3 and 2.5 eV. Results show that 91% and 89% of degradation is achieved within 30 min and 90 min under the microwave and UV irradiation respectively. Hydroxyl radicals (•OH) and superoxide (•O₂⁻) radicals are responsible for photocatalytic degradation of the drug Bactrim DS which is confirmed by radical scavenging experiments. The nanohybrids show promising catalytic activity under UV as well as microwave irradiation.

The current research reports an efficient methodology of new sorbent (SSBC) synthesis based on neglected sepia shells for the sequestration of cationic dye (Methylene blue, MB) and an anionic dye (Reactive black 5, RB5) from aqueous solutions. The as-synthesized SSBC was produced by reaction of sepia shell powder with urea in the presence of formaldehyde. In the first part of the work, the sorbent was scrutinized by using scanning electron microscopy, energy-dispersive X-ray analysis, Fourier transform infrared spectrometry, and titration (for determining pHPZC). In the second step, the influence of several parameters including pH effect, sorbent dosage, temperature, and ionic strength on the two dyes’ sorption effectiveness was examined. The sorption isotherms and uptake kinetics were analyzed at the optimum pH. Outlined results showed that the dynamic experimental obtained data followed the Langmuir isotherm profile, while the kinetic profile fitted well to the pseudo-second-order rate equation. Maximum sorption capacities reach up to 0.794 mmol g⁻¹ (254.05 mg g⁻¹) for MB and 0.271 mmol g⁻¹ (269.18 mg g⁻¹) for RB5, at pH 10.5 and 2.3, respectively. By comparing the sorption properties at different temperatures, the endothermic nature of the sorption process was revealed. Sorption processing under microwave irradiation (microwave-enforced sorption, MES) enhanced mass transfer, and a contact time as low as 1 min is sufficient under optimized conditions (exposure time and power) reaching equilibrium, while 2–3 h was necessary for a “simple” sorption. Dye desorption was successfully tested using 0.5 M solutions of NaOH and HCl for the removal of RB5 and MB, respectively. The as-prepared sorbent can be reused for a minimum of 4 cycles of sorption/desorption. Finally, the sorbent was successfully tested on spiked tap water and real industrial wastewater.

The degradation of methyl orange (MO) in aqueous solution by microwave irradiation in the presence of granular-active carbon (GAC) was investigated. It was found that a synergistic rather than an additive effect of microwave irradiation and GAC contributes to the high-degradation efficiency. The ultraviolet and visible spectrum (UV–vis), infrared spectroscopy (IR), and scanning electron microscopy (SEM) measurements were conducted to trace the MO degradation process. It was demonstrated that the decrease in performance of GAC after repetitive use is largely attributed to the adsorption of some intermediate products on the surface of GAC. The regeneration of the spent GAC under microwave radiation was also investigated. The results show that the activity of spent GAC can be effectively recovered by microwave radiation and 74.1 % of its initial activity remains after six reaction cycles.