How the Unruh effect affects transition between classical and quantum decoherences

We investigate how the Unruh effect affects the transition between classical and quantum decoherences for a general class of initial states and find that: $(i)$ The quantum decoherence exists while $\lambda t\leq\lambda \widetilde{t}$ (the transition time) and the classical one can also affect the system's evolution while $\lambda t\geq\lambda\widetilde{t}$ for both the bit and phase-bit flips, which are different from the cases in inertial frame; $(ii)$ The classical correlations will be different constants corresponding to different Unruh temperature and the quantum decoherence still dominates the evolution of system as $\lambda t\geq\lambda\widetilde{t}$ for the phase flip; And $(iii)$ as the Unruh temperature increases, the $\lambda\widetilde{t}$, compared with that in inertial frame, will be bigger for phase flip but smaller for bit flip. However, the $\lambda\widetilde{t}$ does not change no matter what the Unruh effect is for phase-bit flip.Comment: 15 pages, 6 figure

Activation of Peracetic Acid by CoFe₂O₄ for Efficient Degradation of Ofloxacin: Reactive Species and Mechanism

Peroxyacetic acid (PAA)-based advanced oxidation processes (AOPs) have attracted much attention in wastewater treatment by reason of high selectivity, long half-life reactive oxygen species (ROS), and wider applicability. In this study, cobalt ferrite (CoFe2O4) was applied to activate PAA for the removal of ofloxacin (OFX). The degradation of OFX could reach 83.0% via the CoFe2O4/PAA system under neutral conditions. The low concentration of co-existing anions and organic matter displayed negligible influence on OFX removal. The contributions of hydroxyl radicals (·OH), organic radicals (R-O·), and other reactive species to OFX degradation in CoFe2O4/PAA were systematically evaluated. Organic radicals (especially CH3C(O)OO·) and singlet oxygen (1O2) were verified to be the main reactive species leading to OFX destruction. The Co(II)/Co(III) redox cycle occurring on the surface of CoFe2O4 played a significant role in PAA activation. The catalytic performance of CoFe2O4 remained above 80% after five cycles. Furthermore, the ecotoxicity of OFX was reduced after treatment with the CoFe2O4/PAA system. This study will facilitate further research and development of the CoFe2O4/PAA system as a new strategy for wastewater treatment

Flame-Retarded Rigid Polyurethane Foam Composites with the Incorporation of Steel Slag/Dimelamine Pyrophosphate System: A New Strategy for Utilizing Metallurgical Solid Waste

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

Fabrication of a Sulfur/Steel Slag-Based Filter and Its Application in the Denitrification of Nitrate-Containing Wastewater

To solve the problems of deep nitrogen removal in wastewater treatment plants and the high value utilization of steel slag in the metallurgical industry, this work aims to prepare a sulfur/steel slag-based filter using the melting method. The melt granulation method and the utilization of metallurgical waste were the main innovations of this work. On this basis, the nitrogen removal performance of the filter media in simulated wastewater and actual wastewater were systematically investigated. Furthermore, the factors affecting the nitrogen removal performance of the filter media were studied, and pilot experiments were carried out. The microbial community in the reactor was also analyzed. The results showed that when the mass ratio of sulfur and steel slag was 9:1, the filter media could remove up to 90% of TN in simulated wastewater at room temperature, with a hydraulic retention time (HRT) of 5–20 h and an influent TN of 21 mg/L. In the simulated wastewater, the effluent NO3−-N was less than 2 mg/L, the SO42− was less than 200 mg/L, and the pH was between 6 and 8. The removal of TN from actual wastewater was also greater than 90% at room temperature under a hydraulic retention time (HRT) of 8–20 h and an influent TN of 8 mg/L. Influence factor experiments were conducted at room temperature, with a C/N of 2:1, a DO of 0.9–1 mg/L, and an HRT of 4 h. The results of the pilot experiment confirmed that the effluent TN was stable below 10 mg/L. The filter media was compounded for practical engineering applications. Microbial community analysis showed that the sulfur autotrophic denitrifying bacterial species Thiobacillus accounted for 3.69% and 5.55% of the simulated and actual wastewater systems, respectively. This work provides a novel strategy for the application of solid metallurgical waste in the field of nitrate-containing wastewater treatment