利用炼钢炉尘制备氧化铁脱硫剂的研究

研究以炼钢废弃炉尘经过助溶酸浸法浸出铁成分,然后利用浸出物制备焦炉煤气脱硫用氧化铁脱硫剂的工艺,探讨了硫酸浓度、反应时间、反应温度、盐酸用量和助溶剂用量等因素对铁浸出率的影响。理化性能评价结果显示制得的脱硫剂能够满足焦炉煤气干法脱硫的工业应用要求。     

MgO改性赤泥复合材料对废水中氮磷的同步回收

为处理高浓度氮磷废水同时实现赤泥资源化利用,通过赤泥负载氧化镁制备高效氮磷回收材料(MgO-RM),用以对废水进行氮磷同步回收.考察了废水初始pH值、废水氮磷比和MgO-RM投加量对氮磷同步回收效果的影响.采用动力学模型和等温吸附模型对回收特性进行了描述,在此基础上利用FTIR、XRD、SEM、BET测试手段对MgO-...     

Catalytic decomposition of low level ozone with gold nanoparticles supported on activated carbon

Highly dispersed gold nanoparticles were supported on coal-based activated carbon (AC) by a sol immobilization method and were used to investigate their catalytic activity for low-level ozone decomposition at ambient temperature. Nitrogen adsorption-desorption, scanning electron microscope (SEM), and X-ray photoelectron spectroscopy (XPS) were used to characterize the catalysts before and after ozone decomposition. The results showed that the supported gold nanoparticles prepared with microwave heating were much smaller and more uniformly dispersed on the activated carbon than those prepared with traditional conduction heating, exhibiting higher catalytic activity for ozone decomposition. The pH values of gold precursor solution significantly influenced the catalytic activity of supported gold for ozone decomposition, and the best pH value was 8. In the case of space velocity of 120000h⁻¹, inlet ozone concentration of 50mg/m³, and relative humidity of 45%, the Au/AC catalyst maintained the ozone removal ratio at 90.7% after 2500min. After being used for ozone decomposition, the surface carbon of the catalyst was partly oxidized and the oxygen content increased accordingly, while its specific surface area and pore volume only decreased a little. Ozone was mainly catalytically decomposed by the gold nanoparticles supported on the activated carbon.     

Relationships of nitrous oxide fluxes with water quality parameters in free water surface constructed wetlands

The effects of chemical oxygen demand (COD) concentration in the influent on nitrous oxide (N₂O) emissions, together with the relationships between N₂O and water quality parameters in free water surface constructed wetlands, were investigated with laboratoryscale systems. N₂O emission and purification performance of wastewater were very strongly dependent on COD concentration in the influent, and the total N₂O emission in the system with middle COD influent concentration was the least. The relationships between N₂O and the chemical and physical water quality variables were studied by using principal component scores in multiple linear regression analysis to predict N₂O flux. The multiple linear regression model against principal components indicated that different water parameters affected N₂O flux with different COD concentrations in the influent, but nitrate nitrogen affected N₂O flux in all systems.     

Toxicity and transfer of metal oxide nanoparticles from microalgae to sea urchin larvae

Nanoparticles (NPs) contained in commercial products are released and enter into the aquatic ecosystem, posing serious possible risks to the environment and affecting the food chain. Therefore, investigating the potential toxicity of NPs on aquatic organisms has become an important issue. This study assessed the toxicity and trophic transfer of metal oxide NPs from marine microalgae (Cricosphaera elongata) to the larvae of the sea urchin Paracentrotus lividus. Larvae (24 h old) were fed on 2000 cell mL^?1 48 h of microalgae contaminated with 5 mg L^?1 of several metal oxide NPs (SiO₂, SnO₂, CeO₂, Fe₃O₄) for 15 days. Larval viability and development were monitored from the 4-arm stage to the 8-arm pluteus stage. A significant decrease in survival was observed in larvae fed with microalgae exposed to SiO₂ and CeO₂ NPs. Abnormal development, characterised by skeletal degeneration and altered rudiment growth, was observed in all larvae fed with contaminated NP algae. Our findings revealed that SiO₂ and CeO₂ NPs exerted a toxic effect in the trophic interaction analysed, by reducing sea urchin larval viability, and all metal oxide NPs induced toxicological effects. In conclusion, metal oxide NPs may enter the food chain and become bioavailable for marine organisms, affecting their development.     

Genotoxic effects of Ag2S and CdS nanoparticles in blue mussel (Mytilus edulis) haemocytes

The use of functionalised metal sulphide nanoparticles (NPs) for nanoremediation and biomedical application is rapidly increasing, which could lead to significant inputs into the marine environment. The potential impact of some NPs on marine organisms is still poorly understood. In the present paper the genotoxic potential of Ag₂S and CdS NPs on Mytilus edulis haemocytes was assessed. MPEG-SH (thiol-terminated methyl polyethylene glycol), was used as capping agent to avoid NPs agglomeration. TEM analysis showed that the Ag₂S NPs size was 13±7 nm, whereas CdS quantum dots had an average diameter of 4±1 nm. DNA integrity was evaluated by Comet assay following exposure to increasing concentration series (0.01–10 mg/L). Both silver and cadmium NPs showed genotoxic effects at the highest dose. MPEG-SH was also found to exert a weak genotoxic activity, suggesting that at least part of the genotoxic potential of functionalised NPs on mussel cells might be attributable to the capping agent. These results confirm the genotoxic potential of Ag₂S NPs for mussel cells and demonstrated, for the first time, that CdS NPs is genotoxic in a marine organism.     

Inhibition of bromate formation by reduced graphene oxide supported cerium dioxide during ozonation of bromide-containing water

GO or RGO promotes bromate formation during ozonation of bromide-containing water. CeO₂/RGO significantly inhibits bromate formation compared to RGO during ozonation. CeO₂/RGO shows an enhancement on DEET degradation efficiency during ozonation. Ozone (O₃) is widely used in drinking water disinfection and wastewater treatment. However, when applied to bromide-containing water, ozone induces the formation of bromate, which is carcinogenic. Our previous study found that graphene oxide (GO) can enhance the degradation efficiency of micropollutants during ozonation. However, in this study, GO was found to promote bromate formation during ozonation of bromide-containing waters, with bromate yields from the O₃/GO process more than twice those obtained using ozone alone. The promoted bromate formation was attributed to increased hydroxyl radical production, as confirmed by the significant reduction (almost 75%) in bromate yield after adding t-butanol (TBA). Cerium oxide (less than 5 mg/L) supported on reduced GO (xCeO₂/RGO) significantly inhibited bromate formation during ozonation compared with reduced GO alone, and the optimal Ce atomic percentage (x) was determined to be 0.36%, achieving an inhibition rate of approximately 73%. Fourier transform infrared (FT-IR) spectra indicated the transformation of GO into RGO after hydrothermal treatment, and transmission electron microscope (TEM) results showed that CeO₂ nanoparticles were well dispersed on the RGO surface. The X-ray photoelectron spectroscopy (XPS) spectra results demonstrated that the Ce³⁺/Ce⁴⁺ ratio in xCeO₂/RGO was almost 3‒4 times higher than that in pure CeO₂, which might be attributed to the charge transfer effect from GO to CeO₂. Furthermore, Ce³⁺ on the xCeO₂/RGO surface could quench Br⋅ and BrO⋅ to further inhibit bromate formation. Meanwhile, 0.36CeO₂/RGO could also enhance the degradation efficiency of N,N-diethyl-m-toluamide (DEET) in synthetic and reclaimed water during ozonation.     

冷冻胁迫对芦荟叶肉细胞原生质体中Ca2+、Na+分布的影响

低温和冻害是造成巨大农业损失和植物死亡的主要逆境因子。为揭示冷冻胁迫对植物细胞中离子分布的影响,选择芦荟细胞原生质体为受试材料,使用离子选择性微电极检测了经冷冻处理后的芦荟原生质体在低渗液中破裂时产生的Ca~(2+)浓度脉冲信号,并同时检测Na~+浓度脉冲信号作为对比。研究了冷冻温度、解冻时间和ZnO NPs处理等因素对冷冻胁迫下芦荟原生质体中Ca~(2+)分布的影响。结果表明,与未经冷冻处理的原生质体相对比,经过冷冻处理的原生质体破裂后,其Ca~(2+)脉冲信号前沿处发生明显的"凹陷",这说明,原生质体中Ca~(2+)分布出现分层现象,靠近细胞中心浓度较高而细胞膜附近浓度较低。这一分层现象在温度为-7℃时开始出现,原生质体解冻5 h后仍未消失。经过ZnO NPs预处理后再进行冷冻的原生质体,其Ca~(2+)脉冲凹陷深度明显减小。而当用ZnO NPs处理解冻后的原生质体时,其Ca~(2+)分层现象消失。冷冻胁迫下芦荟原生质体内Ca~(2+)分布发生显著变化,表明原生质体内Ca~(2+)分布变化与其抗寒反应存在一定关系。与Ca~(2+)相反,Na~+的分布几乎不受冷冻因素的影响。ZnO NPs处理对冷冻芦荟原生质体中Ca~(2+)浓度分布分层有明显的缓解作用,表明一定浓度范围的ZnO NPs在缓解冷冻造成的Ca~(2+)流动性下降,维持细胞Ca~(2+)分布的调控能力方面,具有一定的积极影响。     

Enhanced catalytic oxidation of 2,4-dichlorophenol via singlet oxygen dominated peroxymonosulfate activation on CoOOH@Bi2O3 composite

• Bi₂O₃ cannot directly activate PMS. • Bi₂O₃ loading increased the specific surface area and conductivity of CoOOH. • Larger specific surface area provided more active sites for PMS activation. • Faster electron transfer rate promoted the generation of reactive oxygen species. • ¹O₂ was identified as dominant ROS in the CoOOH@Bi₂O₃/PMS system. Cobalt oxyhydroxide (CoOOH) has been turned out to be a high-efficiency catalyst for peroxymonosulfate (PMS) activation. In this study, CoOOH was loaded on bismuth oxide (Bi₂O₃) using a facile chemical precipitation process to improve its catalytic activity and stability. The result showed that the catalytic performance on the 2,4-dichlorophenol (2,4-DCP) degradation was significantly enhanced with only 11 wt% Bi₂O₃ loading. The degradation rate in the CoOOH@Bi₂O₃/PMS system (0.2011 min⁻¹) was nearly 6.0 times higher than that in the CoOOH/PMS system (0.0337 min⁻¹). Furthermore, CoOOH@Bi₂O₃ displayed better stability with less Co ions leaching (16.4% lower than CoOOH) in the PMS system. These phenomena were attributed to the Bi₂O₃ loading which significantly increased the conductivity and specific surface area of the CoOOH@Bi₂O₃ composite. Faster electron transfer facilitated the redox reaction of Co (III) / Co (II) and thus was more favorable for reactive oxygen species (ROS) generation. Meanwhile, larger specific surface area furnished more active sites for PMS activation. More importantly, there were both non-radical (¹O₂) and radicals (SO₄⁻•, O₂⁻•, and OH•) in the CoOOH@Bi₂O₃/PMS system and ¹O₂ was the dominant one. In general, this study provided a simple and practical strategy to enhance the catalytic activity and stability of cobalt oxyhydroxide in the PMS system.     

Comparison of phytotoxic effects of bio-synthesised copper oxide nanoparticle and ionic copper on Elodea canadensis

This study aims to investigate the phytotoxic effects of both Punica granatum peel extract directed copper oxide nanoparticles (CuONPs) and copper nitrate on Elodea canadensis. The CuONPs were characterised by UV–visible spectroscopy (UV-Vis), Dynamic Light Scattering (DLS), X-ray Diffraction (XRD), Scanning Electron Microscope (SEM), and Fourier Transform Infrared (FT-IR) Spectroscopy. The ratio of photosynthetic pigments, total soluble protein, malondialdehyde (MDA), catalase (CAT), ascorbate peroxidase (APX), and copper accumulation in the E. canadensis was determined to evaluate the phytotoxicity of the CuONPs and copper nitrate on E. canadensis. The significant improvements were observed in the growth rate of E. canadensis, chlorophyll a and b, carotenoid contents, and total soluble protein in the E. canadensis when it was exposed to the CuONPs. Additionally, CAT and APX activities and MDA contents were enhanced by accumulation of the CuONPs into the E. canadensis. These results suggested that oxidative stress was alleviated, owing to the result of an increase in the antioxidants such as CAT and APX, with an increase in the concentration of the CuONPs. Finally, the findings of this study show that copper nitrate has many negative effects on E. canadensis compared bio-synthesised CuONPs.