Cholesterol‐imprinted polymer receptor prepared by a hybrid imprinting method

A novel cholesterol‐imprinted polymer (CMIP‐H) was prepared by a hybrid method of covalent imprinting and non‐covalent imprinting. This approach involves the copolymerization of a template‐containing monomer, cholesteryl 2‐hydroxyethyl methacrylate carbonate, and a cross‐linker, followed by hydrolysis to afford a flexible guest‐binding site accompanied with the easy and efficient removal of a ‘sacrificial spacer’. The effect of solvent on the binding capacity of CMIP‐H towards cholesterol was studied, indicating that a good binding capacity towards cholesterol could be achieved in a less‐polar solvent. The binding experiments of CMIP‐H towards a series of structural analogues of cholesterol, including cholesterol acetate, progesterone and stigmasterol, were carried out in hexane. The results showed that CMIP‐H almost did not bind cholesterol acetate at all because the hydrogen‐bonding site is blocked. It exhibited a similar binding towards both cholesterol and stigmasterol, but much higher binding towards progesterone. Copyright © 2005 Society of Chemical Industry     

Probing the early stages of polymerization of ethylene on a model chromium/silica catalyst by Fourier transform infrared spectroscopy

The nature of the interaction of monomer, and the early stages of growth of oligomers of ethylene on a rather more uniform surface of Cr/SiO₂ catalyst than hitherto studied has been investigated by differenceFTIR spectroscopy using C₂D₄ and C₂H₄ as reactants both with and without subsequent treatment of the catalyst with CO andTHF. The active catalyst was prepared by reaction of vapour phase CrO₂Cl₂ with the vicinal hydroxyls of the silica surface. Three distinct kinds of methylene groups were detected. Arguments are given for assigning the peaks at 2935 and 2860 cm^–1 to CH₂ groups directly bound to the active site and those at 2920 and 2850 to CH₂s in the growing chain well removed from the Cr. The peaks at 2160 and 2165 cm^–1 are attributed to CD₂ groups hydrogen bonded to surface hydroxyls.     

铁路站段用交流不间断电源供电系统

结合铁路站段的特点 ,介绍了一种交流不间断电源供电系统 ,能够很好的解决其供电问题。     

DG抗高温隔离液在古深1井的应用

古深1井是大庆油田在古龙地区的一口风险探井,设计井深5 500 m,实际完钻井深为4 739 m。钻进过程中,多次出现塌、漏、卡等事故,造成井径不规则。为平衡压力,压稳地层,更好地隔离钻井液和水泥浆,提高顶替效率,设计采用DG抗高温隔离液。DG抗高温隔离液抗高温可达150℃,密度调节范围宽,抗高温悬浮稳定性好,失水量少,与水泥浆和钻井液相容性好。古深1井采用双级注水泥工艺,固井施工过程十分顺利,隔离液密度均匀,泵送容易,无发泡现象。从声幅测井情况来看,水泥面上部与隔离液交界处界面清楚,水泥环胶结良好,水泥返高达到了设计要求,混浆过渡段短,固井质量合格。     

Effect of intensified discharge in the vicinity of ribs on PDP performance

It was determined that the discharge in the vicinity of ribs should be intensified to obtain low‐voltage, high‐luminous efficacy, and high module efficiency. One possible way is to increase the space between ribs and the discharge surface. Even if the amount of space increases by only 2 or 3 µm, it still results in low discharge voltage, large discharge current, and high luminous efficacy. For that reason it might be important to control the micron‐sized particles included in the MgO crystal dispersed layers. Another preferable way is to use ribs with a low electric permittivity (ε) that are represented by porous ribs. Moreover, low‐ε ribs diffuses the high‐energy spots in plasma, resulting in a high luminous efficacy. They feature a significantly lower sustain voltage and a smaller parasitic capacitance as well to facilitate a help high module efficiency. Also, highly porous ribs are expected to increase their practical use in aspects of mechanical strength and impurity gas exhaustion.     

不同晶型纳米二氧化锰制备及对亚甲基蓝吸附性能

以高锰酸钾（KMnO₄）为氧化剂、硫酸亚铁铵[（NH₄）₂Fe（SO₄）₂]为还原剂,用水热氧化还原反应制备了层状δ-二氧化锰和隧道型α-二氧化锰纳米材料。用X射线衍射（XRD）、扫描电镜（SEM）和氮气吸-脱附技术对产物的晶型、形貌及孔结构进行了表征。实验结果表明,δ-二氧化锰呈花状微球形貌,具有介孔结构（平均孔径为3.4 nm）,BET比表面积为219 m²/g;α-二氧化锰呈纳米线束形貌,具有部分介孔结构（平均孔径为35.7 nm和154.6 nm）,BET比表面积为26 m²/g。研究了不同晶型纳米二氧化锰对亚甲基蓝的吸附性能。实验结果表明,在相同条件下α-二氧化锰的吸附性能优于δ-二氧化锰,且在碱性环境下吸附效果较好。当反应时间达到120 min时,α-二氧化锰和δ-二氧化锰对亚甲基蓝的去除率分别为84.4%和82.9%。     

采用有限元分析法量化不同中空玻璃边缘密封的热位移

间隔条和玻璃板片之间的相对热位移是中空玻璃边缘密封乃至中空玻璃(IGU)本身老化的主要原因之一.作者采用有限元分析法(FEA),建立了发生在大尺寸(1.5 m×2.1 m)的中空玻璃边缘密封的热位移与温差变化之间的模型,这是三种商业化的、不同材质的、不同设计的间隔条,在温度变化为-30～ 60℃范围内的模型.此模型是基于铝间隔条和镀锌钢间隔条与尼龙插角的搭配,不锈钢间隔条和弯曲插角的搭配.尼龙插角假定为实心的并稳固地固定于间隔条上;弯曲插角被建模成实心弯曲的金属插角,并同样稳固地固定于间隔条上.由于实际的弯曲插角是空心的,模型可能高估了这种转角设计的应力.正如预期那样,在低温时,插角会被向内拉,导致弯曲角度大于90°;在高温下,插角会被向外推,导致弯曲角度小于90°.通过检测发生在中空玻璃周边第一道密封的聚异丁烯密封胶厚度的变化,作者发现,到目前为止,不锈钢间隔条对于截面积的变化影响最小;铝制间隔条的影响最大.这个发现与基于间隔条材料与浮法玻璃之间热膨胀系数差异而预期的性能一致.因此,热位移引起的第一道密封的有效扩散横截面变化,可以解释为何具有不同间隔条材料的中空玻璃之间的性能差异.     

Synthesis and biological activity of phthalimide‐based polymers containing 5‐fluorouracil

The attachment of anticancer agents to polymers is a promising approach towards reducing the toxic side‐effects and retaining the potent antitumour activity of these agents. A new tetrahydrophthalimido monomer containing 5‐fluorouracil (ETPFU) and its homopolymer and copolymers with acrylic acid (AA) and with vinyl acetate (VAc) have been synthesized and spectroscopically characterized. The ETPFU contents in poly(ETPFU‐co‐AA) and poly(ETPFU‐co‐VAc) obtained by elemental analysis were 21 mol% and 20 mol%, respectively. The average molecular weights of the polymers determined by gel permeation chromatography were as follows: M_n = 8900 g mol^?1, M_w = 13 300 g mol^?1, M_w/M_n = 1.5 for poly(ETPFU); M_n = 13 500 g mol^?1, M_w = 16 600 g mol^?1, M_w/M_n = 1.2 for poly(ETPFU‐co‐AA); M_n = 8300 g mol^?1, M_w = 11 600 g mol^?1, M_w/M_n = 1.4 poly(ETPFU‐co‐VAc). The in vitro cytotoxicity of the compounds against FM3A and U937 cancer cell lines increased in the following order: ETPFU > 5‐FU > poly(ETPFU) > poly(ETPFU‐co‐AA) > poly(ETPFU‐co‐VAc). The in vivo antitumour activities of all the polymers in Balb/C mice bearing the sarcoma 180 tumour cell line were greater than those of 5‐FU and monomer at the highest dose (800 mg kg^?1). © 2002 Society of Chemical Industry     

Photocatalytic microreactor study using TiO2-coated porous ceramics

Two kinds of porous ceramic disks, having through-holes with diameters of 0.1 and 0.05 mm, were coated with TiO₂ using two different starting solutions: titanyl(IV)acetylacetonate and a commercial titania sol (STS-01). The morphology of these porous ceramics before and after TiO₂ coating was observed by SEM. The TiO₂-coated porous ceramics were examined as honeycomb photocatalytic microreactors. The photocatalytic activity was evaluated using the decomposition of methylene blue solution for radiation angles of 0° and 10° with respect to the pore axis. The highest photocatalytic activity was obtained for the porous ceramic having the pore diameter of 0.1 mm, coated with titanyl(IV)acetylacetonate and irradiated with a light angle of 0° with respect to the pore axis.