曝气生物流化床处理炼油厂含硫和高氨氮污水的研究

炼油厂含硫污水因含高浓度的油、COD、硫化物及挥发酚而难于生化降解，催化剂生产中排放的污水因含高浓度的氨氮、盐类、悬浮物质以及低浓度的有机物而成为水处理的难题．本文采用一种曝气生物流化床（ABFT）工艺，对含硫污水和催化剂高氨氮污水的混合污水进行了现场连续试验，结果表明：在混合污水COD为2090mg／L、氨氮为600mg／L、挥发酚为27mg／L和硫化物为154mg／L的情况下，ABFT系统出水COD为95mg／L、氨氮为4．0mg／L、挥发酚为0．30mg／L和硫化物为0．0067mg／L，出水达到了国家污水排放标准一级标准．在处理工艺中，动态氧化和混凝沉淀作为预处理，ABFT反应器采用了合成高分子载体固定化微生物技术，该载体具有大孔网状以及优良的机械强度和化学性能，高效微生物B350通过化学键固定在载体上．克氏定氮法表明，ABFT中生物负载量为32mg／L．试验结果显示：在处理高氨氮污水方面，ABFT工艺比SBR工艺具有更强的优势，同时，ABFT系统具有较高的处理效率和耐冲击负荷能力．     

γ-Al2O3载体孔内原位合成水滑石

以尿素为沉淀剂,利用γ-Al2O3的内孔表面铝源原位合成水滑石. 考察了晶化时间、晶化温度、初始溶液浓度、原料配比对原位合成水滑石的影响. 实验中发现晶化6 h,MgAlCO3-LDH的晶体结构已趋于完整,晶化时间大于6 h时会有NH4Al(OH)2CO3*H2O杂相生成.在实验条件范围内,生成的一次粒子大小随着晶化时间的延长逐渐增大,随着晶化温度的升高、初始溶液浓度的增大而减小.     

A carbon- and oxygen-isotope record of recent environ- mental change from Qinghai Lake, NE Tibetan Plateau

An understanding of natural climatic variability is essential for evaluating anthropogenic impacts on recent and future climate[1—3]. Due to the lack of lengthy instrumental records, such an understanding must be gained from natural archives of climate change. Palaeolimnological indicators of past lake levels may provide a sensitive record of changes in effective precipitation in closed basins. This approach is particularly relevant on the Tibetan Plateau, where instrumental records are very…     

幽门螺杆菌感染治疗的进展

<正> 近几年深入研究得出了惊人的结果:约96％十二指肠溃疡和约70％胃溃疡应做为感染性疾病采观察。老的观点“无酸—无溃疡”扩展为“无酸或无幽门螺杆菌—无溃疡”根据这个结论,最常见多发胃十二指肠溃疡通过一段时间治疗是可以长期治愈的,众多深入研究明确指出:治愈幽螺杆菌感染可以进一步完全修复胃十二指肠溃疡底部粘膜从而加速治愈溃疡。首先是使对治疗不敏感的溃疡治愈,特别是在根除幽门螺杆菌后消化性溃疡稳定缓解,溃疡复发率几乎为零。相比之下幽门螺杆菌阻性的胃溃疡复发率为50％,十二指肠溃疡复发率70％～90％。并且在根除幽门螺杆菌后能减少溃疡并发症。对初发的胃十二指肠溃疡是否应该抗菌治疗仍有争议(表1)。     

各向异性的气体-颗粒介质内的二通量辐射传热模型

二通量模型是计算气体-颗粒平板内辐射热通量的简化方法. 在最初的二通量模型中, 辐射场被假设成在半球方向的各向同性. 但是对于燃烧领域的气体-颗粒混合介质, 颗粒的散射通常都是各向异性的, 这样, 原有的二通量模型就会由于忽略各向异性而产生严重的误差. 文中一个多层四通量模型被运用到包含气体-颗粒混合物的辐射热通量的计算. 给出了模型的解析求解过程, 定义了等价的平均交叉系数h和前向散射率z来描述整个平板散射的各向异性. 为了验证模型的准确性, 计算了一个无限大平板内的辐射传递过程, 并与解析结果进行了比较. 结果表明提出的模型能够得到准确的结果, 对原有的二通量模型具有较好的改进作用. 运用本模型计算含有飞灰/CO₂/H₂O的燃烧产物的辐射传递, 所得到的平板发射率与Goodwin的经典结果相吻合.     

新型层状农药缓/控释材料—草甘膦插层双金属氢氧化物的超分子结构与缓释性能

以镁铝双金属氢氧化物(MgAl layered double hydroxide: MgAl-LDH)为主体, 以草甘膦(Glyphosate: GLY)为客体, 通过控制反应pH值, 由共沉淀法组装得到两种不同结构的GLY插层MgAl-LDH缓/控释材料. 考察了该缓/控释材料在Na₂CO₃溶液中的缓释性能, 其缓释历程为客体阴离子与介质中CO₃^2-的离子交换过程, 客体阴离子在插层化合物层间及晶粒间隙的扩散, 即粒内扩散过程为释放速率控制步. 低pH合成GLY插层产物较大的层间距、层间客体GLY阴离子单层垂直的定位方向及较高的堆积密度使其较高pH合成材料展示出更为显著的缓释能力, 其原因归结为超分子结构对释放速率控制步的影响. 该研究指出了层状双金属氢氧化物在农药缓/控释领域的应用潜力.     

Nanoengineering of amino - functionalized mesoporous silica nanospheres as nanoreactors

Selective functionalization of mesoporous silica nanospheres (MSNs) is crucial for nanoengineering of MSNs. Herein, we have combined “surface-protected etching strategy” and “cationic surfactant assisted etching strategy” to prepare functionalized MSNs with externally attached amino groups. The externally attached NH2 groups endow the catalysts with excellent catalytic performance for nitroaldol reaction between nitromethane and benzaldehyde. In addition, those NH2-MSNs can also be used to support gold nanoparticles, which display very good catalytic performance for reduction of 4-nitrophenol. It can be envisioned that the synthesis protocol developed in this work could also be extended to nanoengineered MSNs, which provides opportunities for nanoreactors design.     

智能场景建模信息系统

场景建模在计算机图形领域中是非常重要的部分。然而，场景建模是一个非常困难的任务，因为需要建模的场景变得越来越复杂，而且传统的几何建模工具并不能很好适应计算机辅助设计。尽管传统场景建模软件提供了非常有趣的工具来减轻设计者的工作，但是他们还得面对很大的困难，这些工具缺乏灵活性，设计师无法使用非完整或不精确的描述来表达他所想象的场景，所以，当前的几何建模软件在实现建模任务之前都要求用户必须对设计的场景有非常精确的概念，这种设计模式并不是真正的计算机辅助。     

Chiral magnetic order at surfaces driven by inversion asymmetry

Chirality is a fascinating phenomenon that can manifest itself in subtle ways, for example in biochemistry (in the observed single-handedness of biomolecules) and in particle physics (in the charge-parity violation of electroweak interactions). In condensed matter, magnetic materials can also display single-handed, or homochiral, spin structures. This may be caused by the Dzyaloshinskii-Moriya interaction, which arises from spin-orbit scattering of electrons in an inversion-asymmetric crystal field. This effect is typically irrelevant in bulk metals as their crystals are inversion symmetric. However, low-dimensional systems lack structural inversion symmetry, so that homochiral spin structures may occur. Here we report the observation of magnetic order of a specific chirality in a single atomic layer of manganese on a tungsten (110) substrate. Spin-polarized scanning tunnelling microscopy reveals that adjacent spins are not perfectly antiferromagnetic but slightly canted, resulting in a spin spiral structure with a period of about 12 nm. We show by quantitative theory that this chiral order is caused by the Dzyaloshinskii-Moriya interaction and leads to a left-rotating spin cycloid. Our findings confirm the significance of this interaction for magnets in reduced dimensions. Chirality in nanoscale magnets may play a crucial role in spintronic devices, where the spin rather than the charge of an electron is used for data transmission and manipulation. For instance, a spin-polarized current flowing through chiral magnetic structures will exert a spin-torque on the magnetic structure, causing a variety of excitations or manipulations of the magnetization and giving rise to microwave emission, magnetization switching, or magnetic motors.     

Clathrate nanostructures for mass spectrometry

The ability of mass spectrometry to generate intact biomolecular ions efficiently in the gas phase has led to its widespread application in metabolomics, proteomics, biological imaging, biomarker discovery and clinical assays (namely neonatal screens). Matrix-assisted laser desorption/ionization (MALDI) and electrospray ionization have been at the forefront of these developments. However, matrix application complicates the use of MALDI for cellular, tissue, biofluid and microarray analysis and can limit the spatial resolution because of the matrix crystal size (typically more than 10 mum), sensitivity and detection of small compounds (less than 500 Da). Secondary-ion mass spectrometry has extremely high lateral resolution (100 nm) and has found biological applications although the energetic desorption/ionization is a limitation owing to molecular fragmentation. Here we introduce nanostructure-initiator mass spectrometry (NIMS), a tool for spatially defined mass analysis. NIMS uses 'initiator' molecules trapped in nanostructured surfaces or 'clathrates' to release and ionize intact molecules adsorbed on the surface. This surface responds to both ion and laser irradiation. The lateral resolution (ion-NIMS about 150 nm), sensitivity, matrix-free and reduced fragmentation of NIMS allows direct characterization of peptide microarrays, direct mass analysis of single cells, tissue imaging, and direct characterization of blood and urine.