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111.
本文用水热法在SiO_2-FeNH_4(SO_4)_2-MTEACl-NaOH-H_2O体系内合成出了用铁全部取代铝的Fe-Si-ZSM-12型沸石分子筛。实验结果表明,Na_2O/SiO_2、MTEA~+/SiO_2和SiO_2/Fe_2O_3比对分子筛的形成和结晶度有很大影响,Fe-Si-ZSM-12的晶化速度比较缓慢,延长晶化时间则容易转化为α-SiO_2。Fe-Si-ZSM-12的X射线衍射谱图与Al-Si-ZSM-12的基本相同,吸附数据表明,其孔径略大于Al-Si-ZSM-12的孔径,热稳定性则劣于Al-Si-ZSM-12的热稳定性。 相似文献
112.
四核钴羰基簇合物Co4(CO)8(μ-CO)2(μ4-PSR)2的合成和晶体结构 总被引:1,自引:0,他引:1
The title compounds Co4(CO)8(μ-CO)2 (μ4-PSR) [R=-CH3, -C2H5, -C(CH3)3,-(CHa)4CH3] were synthesized by the reaction of Co2(CO)8 with RSPCl2. They were characterized by IR, 1HNMR, elemental analysis. The crystal and molecular structure of Co4(Co)8(μ-CO)2 (μ4-PSC2H5) has been determined by single crystal diffraction method. Crystal data: monoclinic, space group P21 /c, with a=8-445(3), 6=8.562(3), c= 17.125(6)Å, β=104.26 (3)' 9 V=1200.1Å3, Z=2, Dc=1.937gcm-3. Its molecular structure contains an octahedral Co4P2 skeleton which consists of a rectangular four cobalt atoms core and the Co4 core is capped above and below by two quadruply bridging PSR ligands. 相似文献
113.
环己烷中苯甲酰苯胺的双重荧光--分子内电荷转移的直接光谱证据 总被引:2,自引:0,他引:2
自从O Connell等[1]报道苯甲酰苯胺(BA)在EPA玻璃体中异常的长波长荧光发射特性以来, 已有众多学者尝试解释该"异常"荧光的发射态性质[2~12]. Kasha等[2~7]认为长波长荧光是质子转移(PT)和电荷转移(CT)两种激发态发射的叠加, 而Azumaya等[8]则认为发射态只包含分子内扭转电荷转移(TICT)态. 应该指出的是, 在上述研究中, 电荷转移态的指认并无有力的实验事实, 而主要是依据与具有CT双重荧光的对二甲氨基苯甲氰[13,14]的类比. 显然, 有关苯甲酰苯胺的长波长荧光发射态的准确性质仍待实验阐明 相似文献
114.
Yu P Lin Y Xiang L Su L Zhang J Mao L 《Langmuir : the ACS journal of surfaces and colloids》2005,21(20):9000-9006
This letter describes the formation and possible electrochemical applications of molecular films of water-miscible imidazolium-based ionic liquids (ILs) on glassy carbon (GC) electrodes. X-ray photoelectron spectroscopy (XPS) and electrochemical results indicate that the water-miscible ILs used in this study can interact with the GC electrode and form molecular films on the electrode surface. The formed molecular films are found to possess striking electrochemical properties such as electrocatalysis toward ascorbic acid (AA) and the capability to facilitate direct electron transfer of horseradish peroxidase (HRP). This demonstration would pave the way for new electrochemical applications of water-miscible ILs and is envisaged to be useful for the investigation of the electrochemical properties of water-miscible ILs in aqueous media provided the same counteranion is used as the supporting electrolyte. 相似文献
115.
土壤中绿黄隆残留量分析方法的研究 总被引:2,自引:0,他引:2
本文确立了土壤中绿黄隆残留量的间接气相色谱分析方法,用0.15mol/L NaHCO3提取土样,二氯甲烷洗涤初步纯化后,在水浴上加热水解,再用二氯甲烷萃取,弗罗里硅土柱净化,最后用气相色谱-电子捕获检测器检测水解产物邻氯苯磺酰胺。土壤中添加回收率78.5%-90.8%,检测极限0.3ng/g。 相似文献
116.
117.
L. G. Lin Y. Wang J. W. Yan Y. Z. Yuan J. Xiang B. W. Mao 《Electrochemistry communications》2003,5(12):995-999
We report an in situ STM study of a potential-dependent long-range surface restructuring of Au(1 1 1) electrode in neat 1-butyl-3-methylimidazolium tetrafluoroborates (BMIBF4) ionic liquid. Au(1 1 1) undergoes a significant long-range surface restructuring upon cathodic excursion to −1.0 V vs. Pt quasi-reference. The restructuring involves the formation of tiny pits, which then develops into a stable worm-like network with an average width of the network grids 2 nm. Electrochemical annealing occurs at the cathodic limit with the presence of a reduction product of cation BMI+. A smooth surface is recovered with the appearance of the typical (√3 × 22) reconstruction of Au(1 1 1). The surface restructuring is reestablished upon anodic excursion to −1.3 V after the adsorbed reduction product is oxidized. The long-range surface restructuring phenomenon is tentatively explained as a result of partial charge transfer to the weakly adsorbed BMI+, which reduces the metal–metal cohesive energy. In addition, the synergetic effect of the counter anion BF4− may also be involved. The results provide a knowledge of Au(1 1 1) electrode behavior in the neat ionic liquid and are beneficial to understanding in situ STM results involving surface morphological changes in such a media. 相似文献
118.
手性5-l-(艹孟)氧基丁内酯并[3,4-d]-3-取代基-异(口恶)唑啉类化合物的合成 总被引:2,自引:0,他引:2
研究了手性元5-(R)-(l-(艹孟)氧基)-2(5H)-呋喃酮与取代苯甲醛肟以次氯酸钙作为氧化剂进行的区域选择性原位1,3-偶极环加成反应,同步生成两个新的手性中心,得到了一系列光学纯丁内酯并[3,4-d]-3-取代基-异(口恶)唑啉类化合物;应用波谱学手段及X射线单晶衍射法确证了产物的绝对构型,并对产物的核磁共振氢谱规律性加以总结. 相似文献
119.
Jun Ping Xiao Qing Xiang Zhou Hua Hua Bai Department of Chemistry University of Science Technology Beijing Beijing China School of Chemistry Environmental Sciences Henan Normal University Henan Key Laboratory for Environmental pollution Control Xinxiang China 《中国化学快报》2007,18(6):714-717
A procedure for the preconcentration of copper was described in this paper using multi-walled carbon nanotubes (MWCNTs) oxidized by potassium permanganate as the adsorbent for the enrichment of trace copper in water samples. Important parameters, such as the sample pH, the concentration and volume of eluent, sample flow rate and volume, and interference of coexisting ions, were investigated. The obtained results indicated that proposed method possessed an excellent analytical performance. The linear range, the detection limit, and precison (RSD) were 1-100 ng/mL (R2 = 0.9993), 0.32 ng/mL and 2.88%, respectively. The results showed that copper could be adsorbed quantitatively on the pretreated MWCNTs with potassium permanganate, and proposed method was very useful in the monitoring of copper in the environment. 相似文献
120.
包覆型纳米铜-银双金属粉研究 总被引:21,自引:0,他引:21
目前,导电胶或者电磁波屏蔽涂料用的导电性填料主要有三类,一是铜粉,二是银粉,三是铜-银双金属粉。铜粉具有来源广、价格低廉、导电性好等优点,但其抗氧化性能弱;银粉导电性与抗氧化性好,但其资源日益匮乏。大量的研究试图通过对铜粉进行表面改性来提高其性能。表面改性有两种方法,一是包膜处理,用SiO2溶胶处理铜粉,铜粉抗氧化性能提高,但其表面导电性能大大降低犤1犦;另一类方法是在铜粉表面覆盖一层导电性能与抗氧化性能均佳的银或金而制成双金属粉末犤2~5犦。制取高性能的铜-银双金属粉是该领域的研究重点。目前获得铜-银双金属粉的方… 相似文献