Fe3O4活化过硫酸盐体系同步去除诺氟沙星和铅

采用Fe₃O₄活化过硫酸盐（PS）同步去除水中的NOR （诺氟沙星）和Pb （II）.探讨了Fe₃O₄投加量、PS浓度、初始pH值和Pb （II）浓度对NOR降解的影响.结果表明,NOR的降解符合伪一级反应动力学,在温度为30℃、NOR初始浓度为5.0mg/L、Pb （II）浓度为1.0mg/L、Fe₃O₄投加量为2.0g/L、PS浓度为1.5mmol/L、初始pH值为7.0的条件下,反应120min后,NOR降解率达90.2%,Pb （II）去除率为99.5%.自由基淬灭实验证实,硫酸根自由基（SO₄^-·）是NOR降解的主要自由基.通过LC-MS分析结果推测了NOR可能的降解路径和中间产物.Fe₃O₄活化PS高级氧化工艺可作为一种同步去除有机污染物和重金属的工艺.     

FeS对CW-MFC系统降解活性艳红X-3B效果及过程的影响

在自行构建的人工湿地-微生物燃料电池(CW-MFC)系统中,以砾石填料为对照,研究了FeS对活性艳红X-3B脱色效果及降解过程的影响.结果表明,加在底层区域的FeS能够显著提高CW-MFC对活性艳红X-3B的脱色效果和系统产电性能.FeS的投加使得系统脱色率在进水活性艳红X-3B浓度200mg/L、葡萄糖浓度100mg/L条件下达到99.83%.在进水活性艳红X-3B浓度100mg/L、葡萄糖浓度200mg/L条件下,FeS组最大功率密度达到0.849W/m³.活性艳红X-3B在系统中的脱色主要发生在底层和阳极区域,由紫外-可见全波长扫描图谱和GC-MS扫描图谱可知FeS在该区域促进了偶氮双键的断裂,并有利于脱色产物苯胺、三嗪结构、萘环结构的进一步降解.     

基于贝叶斯的苯并(α)芘PBPK模型优化与健康风险评估应用

应用基于生理的药代动力学(PBPK)模型预测苯并(α)芘(BaP)暴露的人体内部剂量,基于贝叶斯的马尔科夫链蒙特卡洛模拟(MCMC)方法对模型参数进行校准和优化,最后运用已优化的模型对BaP内暴露基准值进行推导.研究发现,基于贝叶斯的MCMC方法对模型后验参数校准后,模型精度明显提高,两个数据集验证结果显示残差平方和分别降低了72%和94%.PBPK模型以BaP和子代谢物3-羟基苯并(α)芘(3-OHBaP)的体内动力学过程为结构基础,模拟BaP体内浓度分布大小为脂肪>肾脏>皮肤>缓慢灌注组织>快速灌注组织>静脉血>肝脏;3-OHBaP体内浓度分布大小为肾脏>快速灌注组织>脂肪>肺>静脉血>缓慢灌注组织>肝脏>皮肤.敏感性分析显示,快速灌注组织-血分配系数对模型输出影响最大,灵敏度系数超过了200%;排泄系数影响最小,只有肾小球过滤率K_BR的灵敏度系数超过了1%.以美国国家环境保护局推荐的参考浓度2.0×10^-6mg/m³为外暴露安全基准值,基于PBPK模型推导了职业暴露的BaP生物监测当量(BE),结果显示BE值为0.405pmol/mol肌酐(尿液3-OHBaP平均浓度),为基于人体内暴露剂量水平进行定量健康风险评估奠定了基础.     

深圳市不同区域大气CO2变化特征与来源分析

于2020年12月1日~2021年12月1日分别在深圳市大学城和路边站两点位对大气CO₂和CO浓度进行了为期1a的观测.本次观测期间内两点位大气CO₂平均浓度分别为432×10^-6和439×10^-6,均呈现了“秋冬季高、春夏季低”的季节变化特征与“昼低夜高”日变化特征,且日变化特征在早晚高峰期受到交通源排放的显著影响.此外,通过引入CO₂和CO的净变化值得到大学城和路边站两点位的ΔCO₂/ΔCO值分别为136.8~184.8、59.0~119.3,结果表明机动车排放对深圳市大气CO₂贡献突出.     

Hydrothermal-treated Pt/Al2O3 as an excellent catalyst for toluene total oxidation

The preparation of highly active supported noble metal catalysts with a low noble metal loading has always been the ultimate goal of researchers working on catalysis. Hydrothermally treated Pt/Al₂O₃ (Pt/Al₂O₃-H) exhibits better catalytic activity than that (Pt/Al₂O₃-C) treated via the conventional calcination approach. At the high space velocity of 100,000 mL/(g∙hr), the temperature that correspond to 50% toluene conversion (T₅₀) of Pt/Al₂O₃-H is 115°C lower than that of Pt/Al₂O₃-C, and the turnover frequency (TOF) value can reach 0.0756 sec⁻¹. The mechanism by which the hydrothermal approach enhances Pt/Al₂O₃ activity has been investigated. The structure associated with the high catalytic activity of Pt nanoparticles (NPs) can be retained via hydrothermal treatment. Furthermore, the support is transformed to AlO(OH) with numerous surface hydroxyl groups, which in turn can facilitate the adsorption of toluene. And the synergistic effects of Pt NPs and AlO(OH) increases the contents of Pt in oxidation state and active oxygen, which are beneficial for toluene oxidation.     

Removal of hexavalent chromium from water by Z-scheme photocatalysis using TiO2 (rutile) nanorods loaded with Au core–Cu2O shell particles

All-solid-state Z-scheme photocatalysts, containing Cu₂O, TiO₂ (rutile), and Au as the electron mediator, were prepared and applied to the reduction of Cr(VI) in aqueous solutions. The Cu₂O–Au–TiO₂ composites were prepared by loading Au core–Cu₂O shell hemisphere particles on TiO₂ (rutile) nanorods using a two-step photocatalytic deposition process. Under ultraviolet–visible (UV–vis) light illumination, the Cu₂O–Au–TiO₂ composites exhibited higher photocatalytic Cr(VI) reduction activities than those exhibited by single TiO₂ (rutile) and Cu₂O. In this reaction, a precipitate containing Cr, which was considered to be Cr(OH)₃, was deposited site-selectively on the Au core–Cu₂O shell particles of the composites, indicating that the reduction site of the composite was Cu₂O, and the reaction proceeded according to the Z-scheme. The Cu₂O–Au–TiO₂ composites also exhibited photocatalytic activity under visible light illumination. The oxidation state of Cu in the Cu₂O–Au–TiO₂ composite gradually changed from Cu(I) to Cu(II) during the photocatalytic Cr(VI) reduction. However the composite maintained its high photocatalytic performance even after oxidation. The role of Au in the Cu₂O–Au–TiO₂ composite was examined by comparing the properties of the Cu₂O–Au–TiO₂ composite with those of the Cu₂O–TiO₂ composite prepared via direct Cu₂O deposition on TiO₂.     

Evidence on the causes of the rising levels of CODMn along the middle route of the South-to-North Diversion Project in China: The role of algal dissolved organic matter

As the biggest inter-basin water transfer scheme in the world,the South-to-North Water Diversion Project（SNWD） was designed to alleviate the water crisis in North China.The main channel of the middle route of the SNWD is of great concern in terms of the drinking water quality.In this study,we tested the hypothesis that the dissolved organic matter（DOM） derived from the planktonic algae causes the rising levels of COD_Mn along the middle route by monitoring data on water quality（2015-20...     

Highly efficient P uptake by Fe3O4 loaded amorphous Zr-La (carbonate) oxides: Electrostatic attraction, inner-sphere complexation and oxygen vacancies acceleration effect

Bimetallic oxides composites have received an increasing attention as promising adsorbents for aqueous phosphate (P) removal in recent years. In this study, a novel magnetic composite MZLCO was prepared by hybridizing amorphous Zr-La (carbonate) oxides (ZLCO) with nano-Fe₃O₄ through a one-pot solvothermal method for efficient phosphate adsorption. Our optimum sample of MZLCO-45 exhibited a high Langmuir maximum adsorption capacity of 96.16 mg P/g and performed well even at low phosphate concentration. The phosphate adsorption kinetics by MZLCO-45 fitted well with the pseudo-second-order model, and the adsorption capacity could reach 79% of the ultimate value within the first 60 min. The phosphate adsorption process was highly pH-dependent, and MZLCO-45 performed well over a wide pH range of 2.0-8.0. Moreover, MZLCO-45 showed a strong selectivity to phosphate in the presence of competing ions (Cl⁻, NO₃⁻, SO₄²⁻, HCO₃⁻, Ca²⁺, and Mg²⁺) and a good reusability using the eluent of NaOH/NaCl mixture, then 64% adsorption capacity remained after ten recycles. The initial 2.0 mg P/L in municipal wastewater and surface water could be efficiently reduced to below 0.1mg P/L by 0.07 g/L MZLCO-45, and the phosphate removal efficiencies were 95.7% and 96.21%, respectively. Phosphate adsorption mechanisms by MZLCO-45 could be attributed to electrostatic attraction and the inner-sphere complexation via ligand exchange forming Zr/La-O-P, -OH and CO₃²⁻ groups on MZLCO-45 surface played important roles in the ligand exchange process. The existence of oxygen vacancies could accelerate the phosphate absorption rate of the MZLCO-45 composites.     

高能重离子辐照下国产RPV钢A508-3的硬化行为

目的 研究在563 K的温度条件下,高能重离子辐照导致国产RPV钢A508-3的硬化行为。方法 使用回旋加速器提供的352.8 MeV Fe²¹⁺对A508-3钢试样进行辐照,使其依次达到0.15、0.30、1.50 dpa的损伤水平。借助辐照终端的梯度减能装置,在样品表面至25 μm的深度范围内产生一个准均匀分布的原子离位损伤坪区,并使用纳米压痕仪和维氏显微硬度计测量了试样的硬度。结果 考虑到压痕尺寸效应的影响,采用Nix-Gao模型对硬度数据进行拟合,由于高能Fe离子产生了较厚的损伤区,辐照试样中的软基效应明显减弱。辐照后的试样出现明显的硬化现象,且随着辐照剂量的增大,硬化增量有饱和趋势。通过辐照前和辐照至0.15 dpa试样的微硬度数据,得出其与纳米硬度之间的线性关系(Hv0=0.85 H0)。结论 借助A508-3辐照前后的硬度数据,计算发现试样的屈服强度增量与辐照剂量之间存在一种幂函数关系,这为A508-3钢中子-离子辐照硬化的映射关系研究提供了基础数据。     

三峡库区消落带落羽杉人工林土壤细菌群落结构多样性及动态变化

消落带是连接陆地与水域的交错地带,具有重要的生态功能,其适生木本植物的种植对消落带土壤的生物地球化学循环起着重要的作用.为探究适生植物对三峡库区消落带环境的适应机制,采用高通量测序技术对消落带退水后适生植物落羽杉(Taxodium distichum)不同生长时期(T1:5月、 T2:7月和T3:9月)的土壤细菌群落组成及多样性进行研究,同时采用PICRUSt2对细菌功能进行预测.结果表明,土壤pH值、硝态氮、铵态氮、土壤蔗糖酶、磷酸酶和脲酶等理化指标随时间变化显著(P<0.05);土壤细菌多样性、丰富度和结构也随时间变化而变化,除Chao1以外,根际土壤细菌的α多样性均表现为：T1>T2>T3,非根际土壤细菌α多样性则表现为：T3>T1>T2. RDA分析表明,影响细菌群落的理化指标主要有土壤pH值、脲酶、铵态氮和硝态氮.所有土壤样本中共检测到细菌60门,其中以变形菌门和酸杆菌门为优势细菌门.根据PICRUSt2预测,代谢是落羽杉土壤细菌群落中普遍存在的基本功能,与C、 N和P有关的各代谢途径存在一定的时间差异.以上研究结果有助于加深对三峡消落带植被修复...