气升式环流反应器实验及三维模拟

利用Fluent软件对气升式环流反应器进行三雏全尺寸的数值模拟,采用欧拉多相流模型和标准k-ε模型模拟反应器内气液两相流动,得到了反应器内流场的详细分布.在此基础上还结合FLOW 3D软件模拟物理流动现象,得到了直观的真实清晰动画,而传统的实验很难测得相关具体的数据.两种数值模拟结果与文献实验值吻合较好,说明了数值模拟的可靠性.     

充油对反式-1,4-聚异戊二烯及其与丁苯橡胶并用胶性能的影响

采用干法充油工艺,将门尼黏度为120的反式-1,4-聚异戊二烯(TPI)充芳烃油37.5份制备充油反式-1,4-聚异戊二烯(OETPI).对TPI、OETPI的生胶、硫化胶及其与丁苯橡胶(SBR)并用硫化胶的性能进行了对比.结果表明,OETPI生胶的硬度、门尼黏度、物理机械性能都比TPI的低;OETPI混炼胶的硫化速率比TPI混炼胶的高;OETPI硫化胶的100%和300%定伸应力、邵尔A硬度、拉伸强度等物理机械性能与TPI硫化胶的相比有所降低;磨耗、压缩生热、压缩永久变形增大.与TPI/SBR混炼胶相比,OETPI/SBR混炼胶具有更高的炭黑分散度,较高的硫化速率;OETPI/SBR并用硫化胶的抗湿滑性比TPI/SBR并用硫化胶明显提高,物理机械性能、滚动阻力和动态生热变化不大,耐屈挠龟裂性能提高.     

间苯二甲酰腙类化合物的合成及阴离子识别研究

以间苯二甲酸为起始原料经酯化、肼解得到相应的间苯二甲酰肼,进一步与芳香醛缩合,合成了6种尚未见文献报道的间苯二甲酰腙类目标化合物,其结构经元素分析、IR、1HNMR确证.利用UV-Vis考查了目标化合物与6种阴离子的识别作用,实验结果表明,部分主体分子能较好的识别F-、CH3COO-,溶液的颜色及吸收光谱均发生很大变化,利用其颜色变化实现了裸眼检测.同时探讨了主体分子与阴离子可能的结合模式.     

高氨氮垃圾渗滤液SBR法短程深度生物脱氮

以实际垃圾填埋场渗滤液为研究对象,应用SBR系统对该类废水短程生物脱氮的可行性进行研究,重点考察了短程生物脱氮实现、稳定及系统的脱氮性能.结果表明,经过95天的运行,SBR系统成功实现并维持了稳定短程生物脱氮,平均亚硝积累率在92.5%以上.获得了稳定的脱氮性能,NH4+-N,TN平均去除率分别在97.2%和91.7%以上.DO、ORP和pH曲线的特征点能够准确判断硝化和反硝化终点,可作为SBR处理垃圾渗滤液短程生物脱氮过程的控制参数.相对于氨氧化菌,亚硝酸盐氧化菌对FA、FNA更敏感,因此两者协同作用抑制亚硝酸盐氧化菌活性,再辅以过程控制,能够准确判断硝化终点,实现NOB从系统硝化菌群中逐渐被淘洗,AOB成为优势菌种的目标,这是系统长期维持稳定短程生物脱氮的决定因素,FISH检测结果证明了这一点.     

还原参数对铁基催化剂F—T合成性能的影响

在浆态床反应器中详细考察了还原参数对工业铁基催化剂在F—T合成反应中的影响。研究结果表明：提高还原气体中CO／H2的比值有助于提高烯烃的选择性;提高还原气体的空速可以提高催化剂的活性,但是烯烃的选择性有所降低;升高还原温度在一定程度上可以提高催化剂的活性,但是温度过高容易造成催化剂积炭活性下降,适宜的还原温度范围为210～260℃。     

Invista PET生产线终聚釜的国产化

介绍了InvistaPET工艺终聚釜国产化过程中的几个关键技术问题,包括材料的选择,加工工艺确定及特殊工装的设计及制造,以及怎样保证筒体的椭圆度和筒体与鼠笼之间所要求的配合公差。     

Mechanical reinforcement of poly(1‐butene) using polypropylene‐grafted multiwalled carbon nanotubes

The mechanical properties of poly(1‐butene) reinforced by pristine multiwalled carbon nanotubes (MWNTs) and polypropylene‐grafted MWNTs (PP‐g‐MWNTs) were evaluated. The incorporation of pristine MWNTs to PB led to an improvement in stiffness, but not in strength, ductility, and toughness. In comparison, PP‐g‐MWNTs were able to improve the stiffness, strength, and toughness of PB significantly, without compromising the ductility. The mechanical properties of PB improved with increasing amount of PP‐g‐MWNTs up to an effective MWNT content of 1.5 wt%. Further increase in the effective MWNT content led to a downturn in mechanical properties due to the existence of MWNTs bundles as observed by microscopy. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Validation of Tuba1a as Appropriate Internal Control for Normalization of Gene Expression Analysis during Mouse Lung Development

The expression ratio between the analysed gene and an internal control gene is the most widely used normalization method for quantitative RT-PCR (qRT-PCR) expression analysis. The ideal reference gene for a specific experiment is the one whose expression is not affected by the different experimental conditions tested. In this study, we validate the applicability of five commonly used reference genes during different stages of mouse lung development. The stability of expression of five different reference genes (Tuba1a, Actb Gapdh, Rn18S and Hist4h4) was calculated within five experimental groups using the statistical algorithm of geNorm software. Overall, Tuba1a showed the least variability in expression among the different stages of lung development, while Hist4h4 and Rn18S showed the maximum variability in their expression. Expression analysis of two lung specific markers, surfactant protein C (SftpC) and Clara cell-specific 10 kDA protein (Scgb1a1), normalized to each of the five reference genes tested here, confirmed our results and showed that incorrect reference gene choice can lead to artefacts. Moreover, a combination of two internal controls for normalization of expression analysis during lung development will increase the accuracy and reliability of results.     

The Role of Cytochrome P450 1B1 in Dibenzo[ a,l ]pyrene-induced Carcinogenesis

In human cells, the most carcinogenic polycyclic aromatic hydrocarbon dibenzo[ a,l ]pyrene (DB[ a,l ]P) forms high levels of DNA adducts through formation of the ( m )- anti -(11 R ,12 S )-diol (13 S ,14 R )-epoxide (DB[ a,l ]PDE) and its metabolic precursor, the ( m )-(11 R ,12 R )-diol. Generation of these adducts results from the catalytic activity of cytochrome P450 (P450) 1A1 and 1B1. Additional adducts such as (+)- syn -DB[ a,l ]PDE-DNA or more polar DNA adducts were detected only after increasing exposure doses of the parent compound or in cells that express P450 1A1. At low concentrations (·;100 nM) exclusively ( m )- anti -DB[ a,l ]PDE-DNA adducts were formed by P450 1B1, which is constitutively expressed in many mammalian tissues. Measurement of DNA binding and mutagenicity of DB[ a,l ]P in V79 cells expressing human P450 enzymes revealed a higher activity of P450 1B1 compared to 1A1 at low concentrations. Treatment of P450 1B1 knockout mice and DNA binding studies with fibroblasts isolated from these animals provided further evidence for the central role of P450 1B1-catalyzed formation of ( m )- anti -DB[ a,l ]PDE-DNA adducts in DB[ a,l ]P-induced carcinogenesis.