Environmental Technology最新文献

Spent lithium battery is a polymetallic waste, and valuable to be recovered as Li-bearing chemical with the barriers of impurities separation, especially Fe and Al. Here in, Li-rich cathode powder was manually disassembled from spent battery, and then recovered as lithiophosphate plate in consideration of effective separation of impure Fe/Al. The powder comprised of 23.2% Fe, 3.2% Al, 5.5% Li and 19.6% P, and then dissolved by azotic acid as Li-rich solution. When the solution was heated to 190°C for 10 h with the supplementary of saccharose, more than 99.9% Fe and 98.9% Al were removed as spherical giniite particles, in accordance with the rest of Fe/Al at the concentrations of 2.1 and 14 mg/L, whilst the loss of Li was less than 1.5%. But without saccharose, the Fe/Al removals only achieved by 99.2% and 52.1%. It is also found that the Fe/Al/Li removal achieved by 99.6%, 96% and 25.3% after adjusting the solution to pH 2.7 by NaOH. After hydrothermal treatment, the rest Li can be recycled as lithiophosphate plate by pH adjustment, in contrast to the recovery efficiency of 98.5% Li. Such method raised a facile route to effectively separate impure Fe/Al from Li-rich cathode powder, and showed promising application in the industrial recovery of spent battery.

This study discussed the effect of ferric salt addition on UV/electro-chlorine advanced oxidation process using a train of electrolytic and UV flow cells with an ozone-free low-pressure mercury vapour lamp (total irradiance:0.60 W at 254 nm). Ferric salt addition enhanced 1,4-dioxane degradation at an electrolytic current of 0.100 A. By contrast, an inhibitory effect of ferric salt addition was observed at a current of 0.500 A. The enhanced accumulation of free chlorine at a current of 0.500 A directly decreased the 1,4-dioxane degradation rate by scavenging reactive radicals like HO˙ and Cl˙. However, at an electrolytic current of 0.100 A, UV irradiance was relatively excessive for electrochemical chlorine production. The excess UV energy enhanced the photoreduction of FeOH²⁺, followed by the Fenton-type reaction of Fe²⁺ and HOCl, which produced HO˙ and consumed free chlorine. As a result, the free chlorine concentration decreased, and the reaction efficiency between the reactive radicals and 1,4-dioxane improved. Thus, the addition of ferric salt to a UV/electro-chlorine system is recommended when the UV irradiance in the system is excessive compared to the electrochemical chlorine supply.

The problem of SO₂ pollution in industrial flue gas has brought great pressure to environmental governance. In this study, a new type of activated carbon fixed bed device was designed and built for flue gas desulfurization. The results showed that activated carbons (AC1-AC5) were microporous activated carbons with abundant functional groups on the surface, and the desulfurization performance was ranked as AC1 > AC2 > AC3 > AC4 > AC5. The specific surface area of AC1 was as high as 624.98 m²/g, and the maximum adsorption capacity was 29.03 mg·g^-1 under the optimum reaction conditions. The Freundlich adsorption isotherm model and Bangham pore diffusion model are more suitable for describing the dynamic adsorption process of SO₂ on AC1. Combined with thermodynamic research, it is shown that the adsorption process of SO₂ is a spontaneous, exothermic, and chaotic reduction process, which is mainly a physical adsorption between single-layer adsorption and multi-layer adsorption. Finally, the desulfurization-washing regeneration cycle experiment results showed that the regeneration rate of AC1 increases with the washing time and washing temperature, up to 95%, which provides data reference for industrial application.

The increasing waste generation trends resulted in growing attention to the technologies that aim to reduce or prevent landfilling. The pyrolysis and gasification of refuse-derived fuel (RDF) allow waste to be turned into new raw materials, like pyrolysis gas and syngas. However, the wet gas cleaning processes result in the production of highly contaminated liquid waste. Phenolic compounds are common constituents of this wastewater and often appear in the wastewater of other industries as well. In this research, the laboratory-scale steam gasification of an RDF char was performed to produce syngas and adsorbent simultaneously. The RDF was previously pyrolyzed at 700 °C maximum temperature in a Hungarian pyrolysis pilot plant with approximately 120 kg h^-1 capacity. In this thermal waste processing plant, the pyrolysis gas is already utilised by burning, but currently, the char ends up in landfills. The gasification of char samples was examined with different steam-to-carbon ratios (0.56, 0.84, and 1.12) and duration (30, 60, and 120 min) at 900 °C. Following gasification, the phenol removal capability of the solid by-products was investigated. The results show that its composition and energetic properties make the produced syngas more suitable to use as a raw material in the chemical industry rather than a fuel. At lower concentrations, the effectiveness of the solid by-product for phenol removal was comparable to commercial activated carbon. These are promising results about producing activated carbon from waste without any chemical treatment.

Rapid and effective simultaneous removal of algal and extracellular organic matter (EOM) is essential for algal blooms water emergency treatment. In this study, a composite material was prepared by physical and chemical interaction between La-montmorillonite (La-MMT) and Mg/Al-layered double hydroxide (LDHs), and its removal effect of algal and extracellular organic matters (EOM) was investigated. The results showed that the removal rate of chlorophyll a (chl-a) was 96.8% within 2 h when the LDHs/La-MMT_2:1 dosage was 1.0 g/L. Three-dimensional fluorescence characteristic spectra and parallel factor analysis showed that the removal of EOM by composite material mainly reflected in the removal of humus-like substances. The reaction heat of composite material for the algal solution was -32.7 J/g. Zeta potential changed from -25.7 mV to -16.9 mV, the main treatment mechanisms of composite material were surface adsorption, complexation precipitation, charge neutralisation, and ion exchange. These findings herein proposed that composite material was a potential and proper treating agent for removing algal cells and EOM from algal blooms water.

The soil application of hydrothermally treated penicillin V fermentation residue (PFR) is attractive but challenged, due to the concern of the resistance risk in soil related to residual antibiotics. In this study, a lab-scale incubation experiment was conducted to investigate the influence of penicillin V on antibiotic resistance genes (ARGs) in PFR-amended soil via qPCR. The introduced penicillin V in soil could not be persistent, and its degradation occurred mainly within 2 days. The higher number of soil ARGs was detected under 108 mg/kg of penicillin V than lower contents (≤54 mg/kg). Additionally, the relative abundance of ARGs was higher in soil spiked with penicillin V than that in blank soil, and the great increase in the relative abundance of soil ARGs occurred earlier under 108 mg/kg of penicillin V than lower contents. The horizontal gene transfer might contribute to the shift of ARGs in PFR-amended soil. The results indicated that the residual penicillin V could cause the proliferation of soil ARGs and should be completely removed by hydrothermal treatment before soil application. The results of this study provide a comprehensive understanding of the resistance risk posed by penicillin V during the application of hydrothermally pretreated PFR.

Dimethylsulfoniopropionate (DMSP) is a vital sulfur-containing compound with worldwide significance, serving as the primary precursor for dimethyl sulfide (DMS), a volatile sulfur compound that plays a role in atmospheric chemistry and influences the Earth's climate on a global scale. The study investigated the ability of four bacterial strains, namely Acidimangrovimonas sediminis MS2-2 (MS2-2), Hartmannibacter diazotrophicus E18^T (E18^T), Rhizobium lusitanum 22705 (22705), and Nitrospirillum iridis DSM22198 (DSM22198), to produce and degrade DMSP. These strains were assessed for their DMSP synthesis ability with the mmtN linked to non-ribosomal peptide synthase (NRPS) gene. The results showed that MS2-2, and E18^T bacteria, which contained the mmtN but not linked to an NRPS gene, increased DMSP production with increasing salinity. The highest production of DMSP was achieved at 25 PSU when either methionine was added or low nitrogen conditions were present, yielding 1656.03 ± 41.04 and 265.59 ± 9.17 nmol/mg protein, respectively, and subsequently under the conditions of methionine addition or low nitrogen, both strains reached their maximum DMSP production at 25 PSU. Furthermore, the strains MS2-2, E18^T, and 22705 with the mmtN gene but not linked to an NRPS gene were found to be involved in DMS production. This research contributes to the understanding of the genes involved in DMSP biosynthesis in bacteria that produce DMSP.

Natural (OP) and iron modified orange peel (Fe-OP) were used for the removal of tetracycline from aqueous solutions in batch and fixed bed column systems. The adsorbents were characterized by infrared spectroscopy (IR) and the morphologies of the surfaces before and after tetracycline removal were determined by scanning electron microscope and the elemental analysis was performed by X-ray dispersive spectroscopy (EDS). The kinetic behaviour showed that the equilibrium was reached in 24 and 10 h for OP and Fe-OP respectively, the data were adjusted to both the pseudo second order and intraparticle diffusion models which indicate a chemisorption mechanism and the adsorption process is controlled by the intraparticle diffusion process. The isotherms showed that the adsorption capacity was eight times higher for Fe-OP than OP and the data were best fitted to the Freundlich model indicating that the materials are heterogeneous. The effect of flow rate, influent concentration and adsorbent mass were determined in the column system. The data were adjusted to the Thomas, Adams-Bohart and Yoon-Nelson models, and the best adjustment of data was with the first one. The adsorption capacities in the column system were about half of those obtained in the batch system. These adsorbents show good properties for the removal of tetracycline from water.

Microbial fuel cells (MFCs) can generate energy while processing organic pollutants, which has a great impact on environmental wastewater treatment applications. In this study, a gel polymer was formed by Co-Fe-N co-doping biochar (Co-Fe-N@BC), which was used as the anode material to improve the electricity generation performance of MFC. The Co-Fe-N@BC material prepared at 900℃ carbonised biomass into more graphitic carbon, and its total resistance (3.56 Ω) was significantly reduced. In the corresponding dual-chamber MFC, the current density was 2.81 A/m², and the power density reached 1181 mW/m² at maximum. Among the materials tested, the Co-Fe-N@BC anode MFC had the highest chemical oxygen demand removal rate and coulombic efficiency, reaching 91% and 13%, respectively. It is proved that MFC with Co-Fe-N@BC anode has the best electrochemical performance.

This study developed a novel constructed wetland (CW) coupled with a magnetic field for treating domestic wastewater, and the magnetic field distribution was solved and optimised by the finite element method. Herein, we investigated the effects of optimising magnetic field optimisation and studied its impact on CW treatment performance and the responses of a microbial community. The optimisation results showed that the average magnetic field strength of the CW unit increases from 3 to 8 mT, and the proportion of areas with magnetic field strength greater than 5 mT also increases from 30% to 74%. The water quality analysis results showed that the removal of chemical oxygen demand (COD) and NH₄⁺-N (p < 0.01) was significantly increased by the magnetic field (average 3 mT), increasing by 12.2% and 8.49%, respectively. Moreover, the removal of COD and NH₄⁺-N (p < 0.01) was more significantly increased by M-VFCW(O) (average 8 mT), increasing by 15.58% and 49.1%, respectively. The magnetic field application shifted significantly the abundance of dominant bacteria in CWs. Relative abundance of dominant bacteria such as Proteobacteria (63.3%), Firmicutes (4.72%) and Actinobacteria (2.11%) that played an important role in organics removal and nitrification and denitrification-related bacteria such as Nitrospirae (1.48%) and Planctomycetes (9.58%) significantly promoted in M-VFCW(O). These results suggest that introducing a magnetic field into CWs may improve organics and nitrogen removal via the biological process, and the optimisation of the magnetic field was significant in enhancing the performance of VFCWs.