Study on the elimination characteristics of smoke particles with different materials using electric agglomeration technology.

Fire smoke, consisting of solid particles and liquid droplets, poses risks of asphyxiation, poisoning, making it a significant contributor to fire-related fatalities and environmental pollution. The exploration of effective smoke control methods represents a vital approach to reducing the threat of fire smoke to public health and safety. This study aims to determine the characteristics of elimination for the fire smoke generated from burning four typical materials, thereby validating the universality of electric agglomeration smoke elimination technology. The results indicate that the elimination efficiency of electric agglomeration varies with the material type of the smoke. The rate of change in smoke transmittance from fast to slow is: polyvinyl chloride (PVC), polystyrene (PS), wood, and styrene butadiene rubber (SBR), respectively. With an external potential of 4 kV, PVC smoke reaches the safe threshold after 12.1 s, while SBR smoke achieves it in just 4.9 s. Analysis of the microscopic morphology of agglomerates with scanning electron microscopy (SEM) reveals that particle size distribution is an important factor affecting electric agglomeration elimination. This is because larger initial particles carry a greater charge, enabling the formation of larger agglomerates for more efficient removal. This study provides theoretical guidance for the practical application of electric agglomeration in eliminating smoke particles.

Comparative study by microwave pyrolysis and conventional pyrolysis of pharmaceutical sludge: Resourceful disposal and antibiotic adsorption.

Compared with conventional pyrolysis, microwave pyrolysis has superior heat transfer performance and promotes the decomposition of organic matter. The paper focuses on the harmless treatment and resource utilization of pharmaceutical sludge (PS) by microwave heating and conventional heating methods. The experimental results showed that the conventional pyrolysis gas is dominated by CO2, CO and H2. For microwave pyrolysis gas, the "microwave effect" promoted secondary cracking of volatile fractions and increases the content of CH4, CxHy, H2 and CO through condensation, aromatization, and dehydrogenation. Conventional pyrolysis oils contained the highest percentage of oxygenated compounds. However, high-temperature microwave radiation accelerated the cleavage of polar oxygenated molecular bonds and long-chain hydrocarbons, thereby increasing the aromatics content of pyrolysis oils. The solid residues obtained from microwave pyrolysis is highly graphitized and porous, with a surface area of 146.2 m2/g. Furthermore, the solid residue was rich in pyridine-N and pyrrole-N that could be utilized for adsorption and catalysis. The MA-600 removes up to 99% of tetracycline (TC) in 6 h. It was also found that the adsorption process of TC by the two pyrolysis residues was consistent with the proposed secondary and Freundlich models.

Pre-Drying of Chlorine-Organic-Contaminated Soil in a Rotary Dryer for Energy Efficient Thermal Remediation.

In response to the current problem of the high energy consumption of direct thermal desorption systems when treating soils with a high moisture content, we propose using the waste heat of the system to pre-dry soil to reduce its moisture. Taking chlorine-organic-contaminated soil as an object, an experimental study on the drying and pollutant desorption characteristics of soil in an indirect rotary dryer was carried out. The results show that the non-isothermal drying process was divided into warm-up and falling rate periods, and no constant period was observed. The higher the rotation speed, the lower the soil outlet temperature and the higher the drying tail gas temperature. Soil outlet and dry tail gas temperatures were lower for soils with a higher moisture content. Benzene and cis-1,2-dichloroethylene are easily desorbed. Therefore, the disposal of dry tail gas should be determined according to the type and concentration of soil pollutants present. The volumetric heat transfer coefficient was found to be 85-100 W m-3 °C-1, which provides a key parameter for the size design of a rotary dryer.

Utilizing waste duckweed from phytoremediation to synthesize highly efficient FeNxC catalysts for oxygen reduction reaction electrocatalysis.

Duckweed is a universal aquatic plant to remove nitrogen source pollutants in the field of phytoremediation. Due to the naturally abundant nitrogen, synthesis of carbon materials from duckweed would be a high-value approach. In oxygen reduction reaction (ORR) of metal-air batteries and fuel cells, non-noble metals and heteroatoms co-doped electrocatalysts with excellent catalytic activity and remarkable stability are promising substitutes for Pt-based catalysts. The first-class ORR performance is determined by appropriate pore structure and active sites, which are strongly associated with the feasible synthesis methods. Herein, a facile one-step synthesis strategy for the transition metals- and nitrogen-codoped carbon (MNxC) based catalysts with hierarchically porous structure was developed. The MNxC (M = Fe, Co, Ni, and Mn) active sites were constructed and FeNxC (D-ZB-Fe) was the best electrocatalyst with excellent ORR performance. Results showed that D-ZB-Fe exhibited an obvious honeycomb porous structure with specific surface area of 1342.91 m2·g-1 and total pore volume of 1.085 cm3·g-1. It also possessed considerable active atoms and sites, where the proportion of pyridine N and graphite N was up to 72.9%. The above feature made for a superior ORR electrocatalytic activity. In specific, the onset and half-wave potential were 0.974 V and 0.857 V vs. RHE (Reversible Hydrogen Electrode), respectively. When compared with performances of commercial Pt/C, the four-electron pathway and relatively low peroxide yield, ca. 5%, were almost equivalent. Furthermore, D-ZB-Fe showed an excellent stability and remarkably methanol tolerance by the durability test. In conclusion, this research provides a new synthesis strategy of electrocatalysts with porous structures and active sites.

Review of low-temperature plasma nitrogen fixation technology.

Nitrogen fixation is essential for all forms of life, as nitrogen is required to biosynthesize fundamental building blocks of creatures, plants, and other life forms. As the main method of artificial nitrogen fixation, Haber-Bosch process (ammonia synthesis) has been supporting the agriculture and chemical industries since the 1910s. However, the disadvantages inherent to the Haber-Bosch process, such as high energy consumption and high emissions, cannot be ignored. Therefore, developing a green nitrogen fixation process has always been a research hotspot. Among the various technologies, plasma-assisted nitrogen fixation technology is very promising due to its small scale, mild reaction conditions, and flexible parameters. In the present work, the basic principles of plasma nitrogen fixation technology and its associated research progress are reviewed. The production efficiency of various plasmas is summarized and compared. Eventually, the prospect of nitrogen fixation using low-temperature plasma in the future was proposed.

Comparative Investigation on Chlorobenzene Oxidation by Oxygen and Ozone over a MnOx/Al2O3 Catalyst in the Presence of SO2.

Catalytic oxidation of volatile organic compounds (VOCs) usually encounters complicated components in flue gas causing severe deactivation that restrict its application in specific conditions. The Cl substitution in chlorobenzene further increases poisoning risks. Ozone assistance has unique superiority that can overcome these bottleneck problems. Herein, this study performs a comparative investigation of CB oxidation by oxygen and ozone over a simple Mn/Al2O3 catalyst. CB conversion suffered from slight deactivation in oxygen atmosphere (from 90 to 70%) and more severe deactivation in the presence of SO2 (from 90 to 45%) at 480 °C. Introduction of ozone successfully attained high CB conversion at low temperature (120 °C) with excellent stability and less byproducts. Especially, CB oxidation by ozone maintained its original conversion in the presence of SO2. The deactivation process was simulated by synthesizing several sulfated catalysts. Direct sulfation on Mn/Al2O3 attained more severe deactivation in CB conversion and CO2 formation than sulfation on the Al2O3 support. Ozone with a strong oxidation property promoted the CB oxidation cycle, facilitated desorption of carbonaceous intermediates, and protected MnOx species from severe erosion, thus exhibiting high and stable performance in CB oxidation.

Improving generation of H2O2 and •OH at copper hexacyanocobaltate/graphene/ITO composite electrode for degradation of levofloxacin in photo-electro-Fenton process.

In this work, copper hexacyanocobaltate was electro-deposited at amino-graphene-coated indium-tin-oxide glass to form multifunctional heterogeneous catalyst (CuCoG/ITO), which was confirmed by field emission scanning microscope, infrared spectra, X-ray diffraction, and electro-chemistry techniques. A novel heterogeneous photo-electro-Fenton-like system was established using CuCoG/ITO as an air-diffusion electrode, in which hydrogen peroxide (H2O2) and hydroxyl radical (•OH) could be simultaneously generated by air O2 reduction. The productive rate of •OH could reached to 70.5 µmol h-1 at - 0.8 V with 300 W visible light irradiation at pH 7.0, 0.1 M PBS. Levofloxacin could be quickly degraded at CuCoG/ITO during heterogeneous photo-electro-Fenton process in neutral media with a first-order kinetic constant of 0.49 h-1.