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.     

用水基表面活性剂乳液回收废白土中蜡的界面张力研究

通过测定液体与废白土粉末之间的接触角及液体与蜡之间的液液界面张力，对水基表面活性剂乳液的溶剂及配方进行了优选，得到最佳的水基面活性剂乳液的组成为：质量分数０．２％的十二烷基苯磺酸钠＋体积分数为２．５％的乙醇＋体积分数为２５％的混合烃（正己烷＋苯，等体积）＋体积分数为７２．５％的水。实验证明，用该水基表面活性剂乳液处理废白土，蜡的回收率可达８０％，同时不破坏白土的颗粒结构。     

混合重金属对硝化颗粒污泥毒性作用的析因实验研究

分别测定了Cu2 、Zn2 和Cd2 对硝化颗粒污泥的单一毒性,采用析因实验研究了二元和三元重金属混合体系对硝化颗粒污泥的联合毒性.结果表明,Cu2 、Zn2 和Cd2 的2 h半抑制浓度EC50分别为95.23、62.11和12.48 mg/L,由析因实验所得的响应曲面模型具有较好的优度(其R2＞0.95),能够对混合体系的联合毒性很好地进行预测,析因实验可以用于环境领域混合体系联合毒性的研究.     

热带海洋环境中5083铝合金腐蚀行为研究

目的 研究某岛礁不同海洋区带环境中5083铝合金的腐蚀规律。方法 在某岛礁进行海洋多区带腐蚀试验,利用表面微观形貌观测、腐蚀产物分析、质量损失测试及点蚀深度测量等手段,对比分析铝合金在不同海洋区带中的腐蚀形貌、腐蚀速率和点蚀深度。结果 5083铝合金在某岛礁海洋全浸区带环境中的腐蚀速率最大,大气区带中的腐蚀速率最小,在潮差区带的腐蚀速率介于二者之间。试样在海洋不同区带主要发生局部腐蚀,大气区试样的最大点蚀深度最大,而潮差区试样的最大点蚀深度最小。在不同海洋区带,铝合金腐蚀产物和附着物的混合物中均含有钙元素,大气区钙元素含量远低于潮差区和全浸区,潮差区和全浸区铝合金表面的腐蚀产物和附着物混合物中主要含有CaCO₃、CaSiO₃和Al₂O₃。结论 不同海洋区带环境中,5083铝合金的腐蚀速率差别较大,潮差区和全浸区材料表面附着大量污损生物和矿物质。