TiO2/SiO2@γ-Fe2O3光催化剂的制备及其光催化性能

以共沉淀法制备的纳米Fe3O4为核,以正硅酸乙酯为硅源,通过溶胶-凝胶法制备了SiO2@Fe3O4壳-核结构纳米颗粒,再以钛酸四丁酯为钛源,通过溶胶-凝胶法、经焙烧制得TiO2/SiO2@γ-Fe2O3磁性纳米光催化剂。采用X射线衍射仪、透射电子显微镜、比表面分析仪、振动磁强计对光催化剂的结构进行了表征,以苯酚溶液为模拟废水对光催化剂的光催化性能进行了评价。实验结果表明:经500℃焙烧的光催化剂活性相为锐钛矿型TiO2;在苯酚溶液初始浓度为0.2mmol/L、苯酚溶液pH为7的条件下,COD去除率为70.9%。     

超临界水氧化法处理造纸黑液

采用自制的超临界水氧化反应装置,对造纸工业排放的黑液进行处理。考察了反应温度、反应压力、反应时间、过氧量(初始反应时所加氧气的量与废水完全氧化所需氧气的理论量的比,%)等对黑液中COD去除率的影响。实验结果表明,处理黑液的最佳反应条件为:反应温度500℃,压力26M Pa,过氧量500%,反应时间120s。在此最佳条件下处理COD为85 000m g/L的造纸黑液,COD去除率可达99.9%。     

基于拉曼光谱的铅致肝细胞生物分子变化研究

利用拉曼光谱技术采集不同铅离子暴露时间(0.5,1.5,3,6,12,24h)、暴露浓度(0.05,0.1,0.5,1,5mg/L)下HepG2细胞的光谱数据,欲探究在不同铅暴露条件下肝细胞的分子变化及其相关机制.研究结果发现,在不同条件下各组细胞的光谱形态基本相同,但部分特征峰的吸光度强度存在差异.经多元统计分析发现,除6h外,同一暴露时间下不同暴露浓度细胞的光谱数据在LD1上均存在离散趋势,并在暴露24h时最明显.细胞内蛋白质、脂质、核酸、类胡萝卜素、碳水化合物等生物分子的特征峰表现出明显差异,但不同类型生物分子发生显著变化的时间并不相同.由此可见铅暴露可损伤肝细胞蛋白质、脂质、核酸、类胡萝卜素的结构并影响其正常功能,这种毒性效应呈剂量-效应关系,且随暴露时间的增加而增加.本研究说明拉曼光谱可以实现铅对肝细胞生物分子变化的相关检测,这不仅为之后的细胞毒理研究提供了新的思路,同时也为环境污染物的安全评价提供了理论依据.     

When apologizing hurts: Felt transgression and restoration efforts

Apologizing is important for conflict resolution and relationship reconciliation, yet apologies often fail to restore the damaged relationship. While much research has been devoted to investigating the victims' reactions upon receiving an apology, in this paper, we adopt an apologizer-centric approach and explore the phenomenon of apologizing with no felt transgression (vis-à-vis when there is felt transgression) along with its affective and reconciliation outcomes for the apologizer. Based on Appraisal Tendency Framework, we predict that apologizing with no felt transgression will lead to reduced guilt and increased anger in the apologizer, which will result in a decreased level of their restoration efforts towards the victim. In addition, we further hypothesize about the role of organizational conflict cultures in influencing the relationship between apologizing and restoration efforts via guilt and anger. Study 1 uses a micro-narrative procedure and an inductive data analysis approach to demonstrate the varied situations and motivations of employees apologizing with (no) felt transgression, Study 2 utilizes an experimental design to examine the mediation effect, and Study 3 employs the critical incident technique to test our whole research model. Our hypotheses were largely supported across our studies. Theoretical and practical implications are discussed.     

城市可持续发展环境经济评价及案例

基于城市发展测度演变的分析、明确真实储蓄作为城市可持续发展综合评价指标的经济学含义和政策意义：并针对世界银行在地区真实储蓄测算方法上的不足,重点探讨在真实储蓄测算中如何考虑城市开放性、资源折旧、环境污染损失评估计算的界定问题。文中还以烟台市为试点城市,利用真实储蓄及相关指标评价了该市不同发展时期的可持续发展水平。     

高锰酸盐复合剂强化饮用水除污染生产性研究

采用依时间序列进行对比的方法,考察了高锰酸盐复合剂(PPC)对饮用水源的强化除污染效能。生产性实验结果表明,PPC具有优良的强化混凝和强化过滤效能,能显著降低水厂沉后水和滤后水的浊度、COD_Mn、UV₂₅₄等水质指标。与未投加时相比较,水厂投加PPC后沉后水和滤后水浊度分别降低了25%和33.3%,沉后水和滤后水COD_Mn去除率分别提高了15.3%和11.5%,UV₂₅₄去除率分别提高了16.3%和9.5%。同时,GC/MS分析表明PPC能有效去除水源水中的多种微量有机污染物,显著提高饮用水的化学安全性。PPC通过高锰酸钾的氧化作用,水合二氧化锰的吸附作用,以及各组分间的协同强化作用,显著提高了对水中污染物质的去除效率。     

Microbial reduction of uranium (VI) by Bacillus sp. dwc-2: A macroscopic and spectroscopic study

The microbial reduction of U(VI) by Bacillus sp. dwc-2, isolated from soil in Southwest China, was explored using transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and X-ray absorption near edge spectroscopy (XANES). Our studies indicated that approximately 16.0% of U(VI) at an initial concentration of 100 mg/L uranium nitrate could be reduced by Bacillus sp. dwc-2 at pH 8.2 under anaerobic conditions at room temperature. Additionally, natural organic matter (NOM) played an important role in enhancing the bioreduction of U(VI) by Bacillus sp. dwc-2. XPS results demonstrated that the uranium presented mixed valence states (U(VI) and U(IV)) after bioreduction, which was subsequently confirmed by XANES. Furthermore, the TEM and high resolution transmission electron microscopy (HRTEM) analysis suggested that the reduced uranium was bioaccumulated mainly within the cell and as a crystalline structure on the cell wall. These observations implied that the reduction of uranium may have a significant effect on its fate in the soil environment in which these bacterial strains occur.     

The role of doped-Mn on enhancing arsenic removal by MgAl-LDHs

To meet the challenges posed by global arsenic water contamination, the MgAlMn-LDHs with extraordinary efficiency of arsenate removal was developed. In order to clarify the enhancement effect of the doped-Mn on the arsenate removal performance of the LDHs, the cluster models of the MgAlMn-LDHs and MgAl-LDHs were established and calculated by using density functional theory (DFT). The results shown that the doped-Mn can significantly change the electronic structure of the LDHs and improve its chemical activity. Compared with the MgAl-LDHs that without the doped-Mn, the HOMO-LUMO gap was smaller after doping. In addition, the -OH and Al on the laminates were also activated to improve the adsorption property of the LDHs. Besides, the doped-Mn existed as a novel active site. On the other hand, the MgAlMn-LDHs with the doped-Mn, the increased of the binding energy, as well as the decreased of the ion exchange energy of interlayer Cl⁻, making the ability to arsenate removal had been considerably elevated than the MgAl-LDHs. Furthermore, there is an obvious coordination covalent bond between arsenate and the laminates of the MgAlMn-LDHs that with the doped-Mn.     

Layered sphere-shaped TiO2 capped with gold nanoparticles on structural defects and their catalysis of formaldehyde oxidation

We describe here a one-step method for the synthesis of Au/TiO₂ nanosphere materials, which were formed by layered deposition of multiple anatase TiO₂ nanosheets. The Au nanoparticles were stabilized by structural defects in each TiO₂ nanosheet, including crystal steps and edges, thereby fixing the Au–TiO₂ perimeter interface. Reactant transfer occurred along the gaps between these TiO₂ nanosheet layers and in contact with catalytically active sites at the Au–TiO₂ interface. The doped Au induced the formation of oxygen vacancies in the Au–TiO₂ interface. Such vacancies are essential for generating active oxygen species (*O⁻) on the TiO₂ surface and Ti^3 + ions in bulk TiO₂. These ions can then form Ti^3 +–O⁻–Ti^4 + species, which are known to enhance the catalytic activity of formaldehyde (HCHO) oxidation. These studies on structural and oxygen vacancy defects in Au/TiO₂ samples provide a theoretical foundation for the catalytic mechanism of HCHO oxidation on oxide-supported Au materials.