Heterogeneous catalysis ozonation technology can achieve efficient treatment of refractory organics in industrial wastewater due to its advantages including fast reaction speed, high ozone utilization rate, low catalyst loss and low cost and has a broad application prospect. The development of efficient and stable heterogeneous ozone catalytic materials is the key to promoting the application of this technology in industrial wastewater treatment. Based on this, an Mn/Al₂O₃ catalyst was successfully prepared by impregnation method using 3~5 mm γ-Al₂O₃ pellets as the carrier, and the surface morphology characteristics, elemental state and phase composition of the catalyst were investigated by SEM-EDX, XRD and XPS. The results showed that Mn was successfully loaded onto the surface of a γ-Al₂O₃ carrier. On this basis, intermittent single factor experiments were conducted to systematically investigate the effects of catalyst dosage, pH, and ozone concentration on the catalytic performance of phenol. It was found that under the optimal conditions of a catalyst dosage of 100 g (filling height of 14.2 cm), pH of 7, and ozone concentration of 4 mg/L (gas volume of 1 L/min), the removal efficiencies of 800 mL 100 mg/L of simulated phenol wastewater reached 100% after 60 min of reaction. The removal efficiencies of the catalyst still reached 95.8% within 60 min even after the fifth cycle reaction, indicating excellent reusability of the catalyst. This work provides a facile strategy for the treatment of refractory organics in industrial wastewater.

The biological treatment efficiency of dye wastewater using activated sludge (AS) is largely limited to the chromaticity and ecotoxicity of dyestuff. To alleviate this limitation, eleven industrial-grade disperse dyes were obtained from a fiber-dyeing factory, and for the first time, we studied the decolorization and detoxification effects of using the Pycnoporus laccase enzyme. Efficient decolorization was achieved with the following conditions: dye concentration 50 mg/L, 1-hydroxybenzotriazole (HBT) 0.15 mM, temperature 65 °C, pH 4, and laccase 0.33 U/mL. The decolorization rate of disperse dyes, ranging from 51 to 96% in this investigation, was highly dependent on the dye type, concentration, laccase loading, and HBT. The ecotoxicity of dyes was evaluated by studying the germination/growth of wheat seed as well as the respiratory rate of aerobic AS. Laccase treatment mitigated the phytotoxicity of dyes because of the higher wheat germination (e.g., increase of 38% for Black ECT 200%) and growth rate (e.g., increase of 91% for Blue 2BLN 200%). The reduced ecotoxicity of decolorized dye solution towards microorganisms was also confirmed by the finding that the oxygen uptake by aerobic AS was increased relative to that of the untreated samples (e.g., increase of 14 folds for Blue HGL 200%). In addition, the chemical oxygen demand (COD) of decolorized dye solution was slightly lower than that without decolorization during the respiratory test. The experimental results suggest that enzymatic decolorization and detoxification can be potentially used as a pretreatment method for disperse dye wastewater followed by AS treatment.

Rigid polyurethane (RPUF) was widely used in external wall insulation materials due to its good thermal insulation performance. In this study, a series of RPUF and RPUF-R composites were prepared using steel slag (SS) and dimelamine pyrophosphate (DMPY) as flame retardants. The RPUF composites were characterized by thermogravimetric (TG), limiting oxygen index (LOI), cone calorimetry (CCT), and thermogravimetric infrared coupling (TG-FTIR). The results showed that the LOI of the RPUF-R composites with DMPY/SS loading all reached the combustible material level (22.0 vol%~27.0 vol%) and passed UL-94 V0. RPUF-3 with DMPY/SS system loading exhibited the lowest pHRR and THR values of 134.9 kW/m² and 16.16 MJ/m², which were 54.5% and 42.7% lower than those of unmodified RPUF, respectively. Additionally, PO· and PO₂· free radicals produced by pyrolysis of DMPY could capture high energy free radicals, such as H·, O·, and OH·, produced by degradation of RPUF matrix, effectively blocking the free radical chain reaction of composite materials. The metal oxides in SS reacted with the polymetaphosphoric acid produced by the pyrolysis of DMPY in combustion. It covered the surface of the carbon layer, significantly insulating heat and mass transport in the combustion area, endowing RPUF composites with excellent fire performance. This work not only provides a novel strategy for the fabrication of high-performance RPUF composites, but also elucidates a method of utilizing metallurgical solid waste.

In this work, a macroporous strongly basic anion exchange resin D201 was used as the matrix and loaded with nano hydrated titanium oxide (HTO) to fabricate a novel resin-based nano hydrated titanium oxide adsorbent (HTO-D201), which was characterized by scanning electron microscope-energy dispersion spectroscopy (SEM-EDS), transmission electron microscope (TEM), X-ray diffraction (XRD) and Brunauer-Emmett-Teller (BET) analysis. Adsorption isotherm, pH influence competitive adsorption and column adsorption experiments were conducted to investigation the adsorption behavior of HTO-D201 to phosphorus in water. The adsorption effect of adsorbent HTO-D201 on phosphorus in water, and the corresponding adsorption mechanism, are discussed. It was observed that HTO-D201 exhibited spontaneous adsorption behavior with Langmuir fitting maximum adsorption capacity of 34.08 mg∙g⁻¹ under a pH of 6.8 and a temperature of 298 K. Adsorption isotherms confirmed that enhancing temperature could promote the adsorption process. SO₄²⁻, NO₃⁻ and Cl⁻ were used as competing ions in competitive adsorption, which confirmed better anti-interference ability of HTO-D201 compared with that of unmodified D201. The column adsorption experiment implied that HTO-D201 possessed a stable structure and good dynamic adsorption performance, with effective processing capacity of 420BV, which could be regenerated and recycled. The adsorption mechanism of HTO-D201 to phosphorus in water is discussed, which was ascribed to a quaternary amine group on the resin and a hydroxyl group on the HTO. This work shows that HTO-D201 is a promising adsorbent that a possesses excellent phosphorus-removing capacity from wastewater and the potential for practical application.

The residual emerging pollutants in secondary effluent from a chemical industry park contain potential risks for natural waters. Herein, the cobalt ferrite/peracetic acid system was employed to destroy aniline, a typical emerging pollutant, with a reaction rate of 0.0147 min⁻¹ at pH 7.0. Singlet oxygen (¹O₂) served as the predominant reactive species for aniline degradation, with superoxide radicals (O₂⁻) and organic radicals (R-O) acting in secondary roles. The valence transition between Co(II) and Co(III) on the CoFe₂O₄ surface played a determining role in the reaction progression. The presence of anions and humic acids with low concentrations had minimal impact on aniline removal. Additionally, the CoFe₂O₄ catalyst demonstrated excellent recyclability, maintaining a pollutant removal rate above 93% over five consecutive cycles. Lastly, the CoFe₂O₄/PAA system demonstrates effective treatment of typical pollutants, including phenolic compounds, pesticides, antibiotics, and dyes, achieving removal rates of 77.48% to 99.99%. Furthermore, it significantly enhances water quality in the treatment of actual secondary effluent, offering a novel theoretical foundation and practical insights for applying this catalytic system in wastewater treatment.