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101.
在分析当前省属工科院校教育以能力为导向培养目标完成实施过程中遇到国际化困难问题的基础上,以青岛大学材料学科为例,提出了基于国际化产科教融合实训平台的教学模式改革举措,并经过实践验证证实其切实可行。包括:充分整合校内外材料学科整体资源,建立了国际化的产科教深度融合实训平台,构建了高效的国际化产科教深度融合协同育人实训平台动态管理运行机制;以实训平台为依托实现师资队伍、教学内容、教学模式、科研等全方位的国际化改革;基于国际化产教研融合实训平台的教学模式改革的实践收到显著成效,对全国省属高等院校理工学科专业建设国际化改革的推广有较好的示范作用。 相似文献
102.
QiLiangDENG ZhiHongLUN ChaoYAN RuYuGAO 《中国化学快报》2005,16(7):955-958
This study concentrated on the production of molecularly imprinted polymers (MIPs) as highly selective sorbents for felodipine (FLD), a representive dihydropyridine calcium antagonists. Demonstrated chromatographically through a selection factor, these MIPs showed high selectivity for the template molecule among a group of structurally similar compounds. The recognition was found to correlate with structural similarity to the template compound. 相似文献
103.
Using cotton as a solid-phase extraction sorbent of the precolumn, an on-line coupled precolumn preconcentration-liquid chromatography system with fluorescence detection was developed for the determination of PAHs in aqueous samples. Four PAHs including fluorene, phenanthrene, fluoranthene and benzo[k]fluoranthene were preconcentrated by a precolumn packed with 30 mg of absorbent cotton and then separated by C18 analytical column. When 100 ml of sample was enriched, the proposed procedure provided detection limits in the range of 0.5-57 ng l−1. Several water samples spiked with PAHs were analyzed with recoveries in the range of 92-119% at spiking level of 100 ng l−1 for fluorene, phenanthrene and fluoranthene, and 10 ng l−1 for benzo[k]fluoranthene, respectively. 相似文献
104.
Changzheng Wu Qing Yang Chao Huang Ping Yin Yi Xie 《Journal of solid state chemistry》2004,177(10):3522-3528
Pure hexagonal aluminum nitride (AlN) nanowhiskers have been successfully synthesized by directly reacting AlCl3 with NaN3 in non-solvent system at the low temperature of 450 °C for 24 h. The obtained products are characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, high-resolution transmission electron microscopy and selected area electron diffraction, which show that the obtained products are hexagonal phase AlN nanowhiskers with width from 10 to 80 nm and length up to several micrometers. The influencing factors of the formation of AlN nanowhiskers were discussed and a possible growth mechanism for AlN nanowhiskers was proposed. Additionally, the study on the corresponding optical properties and catalytic properties is also carried out. 相似文献
105.
106.
合成了一种含吡唑啉酮的三脚架结构化合物 1,1,1 三 { 1′ [2′ 氧杂 5′ 氧代 5′ ( 1″ 苯基 3″ 甲基吡唑啉酮 4″ 基 )戊基 ] }丙烷 (H3 L)及其 7个稀土配合物。通过元素分析、摩尔电导、质谱、红外光谱、核磁共振谱、荧光光谱等对H3 L及其稀土配合物的组成及性质进行了表征。分析结果表明 :H3 L的分子式为C45H50 N6O9,配合物的组成比为REL·0 5H2 O (RE =La ,Sm ,Eu ,Gd ,Tb ,Dy ,Yb) ;该三脚架形配体分别以醚氧、烯醇氧及吡唑酮环上的羰基氧与稀土离子进行配位 ,形成内配型配合物。荧光光谱分析表明SmL·0 5H2 O ,EuL·0 5H2 O ,TbL·0 5H2 O ,DyL·0 5H2 O配合物具有三价稀土离子的特征线状荧光 ,其中TbL·0 5H2 O的荧光强度最强 ,表明T(配体 )→5D4(Tb)能级更为匹配 ,从而进行分子内能量有效传递 ;由EuL·0 5H2 O的荧光光谱图形推测 ,Eu3 +离子在该配合物中处于非对称中心 相似文献
107.
meso -四 (α ,α ,α ,α - 0 -苯乙酰苯 )卟啉诱导的单抗 (MAb)导致meso -四 (α,α ,α ,α - 0 -苯乙酰苯 )卟啉Soret带来巨大红移 ,并且在meso -四 (α ,α ,α ,α - 0 -苯乙酰苯 )卟啉上产生巨大的诱导Cotton效应 (ICD) .借用ICD定量分析meso -四 (α ,α ,α ,α - 0 -苯乙酰苯 )卟啉同抗体的结合 ,表明在抗体超过meso -四 (α ,α ,α ,α - 0 -苯乙酰苯 )卟啉的情况下 ,既有 1∶1结合 ,又有 2∶1结合〔结合位点 :meso -四 (α ,α ,α ,α - 0 -苯乙酰苯 )卟啉〕 相似文献
108.
Changlun Chen Di Xu Xiaoli Tan Xiangke Wang 《Journal of Radioanalytical and Nuclear Chemistry》2007,273(1):227-233
The fate and transport of toxic metal ions and radionuclides in the environment is generally controlled by sorption reactions.
The extent of sorption of divalent metal cations is controlled by a number of factors including cosorbing or complexing. In
this work, the effects of pH, humic acid HA/Co(II) addition orders, ionic strength, concentration of HA, and foreign cations
on the Co(II) sorption on γ-Al2O3 in the presence of HA were investigated. The sorption isotherms of Co(II) on γ-Al2O3 in the absence and presence HA were also studied and described by using S-type sorption model. The experimental results showed
that the Co(II) sorption is strongly dependent on the pH values, concentration of HA, but independent of HA/Co(II) addition
orders, ionic strength, and foreign cations in the presence of HA under our experimental conditions. The results also indicated
that HA enhanced the Co(II) sorption at low pH, but reduced the Co(II) sorption at high pH. It was hypothesized that the significantly
positive influence of HA at low pH on the Co(II) sorption on γ-Al2O3 was attributed to strong surface binding of HA on γ-Al2O3 and subsequently the formation of ternary surface complexes such as ≡S-OOC-R-(COO−)
x
Co2−x
. Chemi-complexation may be the main mechanism of the Co(II) sorption on γ-Al2O3 in the presence of HA. 相似文献
109.
Constituting the artificial carbon cycle,for example,through recycling CO2 and converting CH4 to value-added fuels and chemicals with solar energy,offers a sustainable future for humankind to tackle the global environmental issues and energy crisis.However,significant bottlenecks remain in such photocatalytic conversion,mainly related to the reaction activity and product selectivity.Herein,we share our efforts and systematic research progress on addressing the double bottlenecks for achieving solar-driven artificial carbon cycle,with specifically focusing on the photocatalytic CO2 and CH4 conversion.We further elucidate the common fundamentals behind various designed photocatalytic materials systems.Toward future development,we highlight the opportunities and challenges in the research field. 相似文献
110.
Fashui?HongEmail author Xuefeng?Wang Chao?Liu Guoxing?Su Weiping?Song Kang?Wu Ye?Tao Guiwen?Zhao 《中国科学B辑(英文版)》2003,46(1):42-50
It was studied by spectroscopy that PSII reaction center complex consisting of three polypeptides, D1, D2 and Cytb559, were purified from PSII particle of CeCl3 treated spinach. The results of the experiment show that Ce3+ could improve the growth of spinach, and accelerate electron transport of PSII particles. Of chl-a of UV-Vis spectrum of
D1/D2/Cytb559 complex, Soret band was blue-shifted by 3 nm and Q band by 2 nm, respectively, and the fluorescence emission
peak was blue-shifted by 5 nm in CeCl3-treated spinach compared with the one in control. By the extended X-ray absorption fine structure (EXAFS) spectroscopy methods,
it has been found that Ce3+ is coordinated with 8 nitrogen atoms in the first coordination shell with Ce-N bond length of 0.253 nm, and Ce3+ with 6 oxygen atoms in the second coordination shell with Ce-O bond length of 0.32 nm. However, the secondary structure of
D1/D2/Cytb559 complex by circular dichroism (CD) spectroscopy has no significant change after CeCl3 treated. It might be that Ce3+ binds to porphyrin rings of chlorophyll and oxygen of amino acid residue of polypeptide in D1/D2/Cytb559 complex, and then
accelerates the primary reaction of PSII, intensifies function of P680+ primary electron donor of D1/D2/Cytb559, but there is little change in conformation of PSII reaction center complex. 相似文献