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101.
以介质填充的平行板放电结构为例,本文主要研究了介质填充后微波低气压放电和微放电的物理过程.为了探究介质材料特性对微波低气压放电和微放电阈值的影响,本文采用自主研发的二次电子发射特性测量装置,测量了7种常见介质材料的二次电子发射系数和二次电子能谱.依据二次电子发射过程中介质表面正带电的稳定条件,计算了介质材料稳态表面电位与二次电子发射系数以及能谱参数的关系.在放电结构中引入与表面电位相应的等效直流电场后,依据电子扩散模型和微放电中电子谐振条件,分别探讨了介质表面稳态表面电位的大小对微波低气压放电和微放电阈值的影响.结果表明,介质材料的二次电子发射系数以及能谱参数越大,介质材料的稳态表面电位也越大,对应的微波低气压放电和微放电阈值也越大.所得结论对于填充介质的选择有一定的理论指导价值. 相似文献
102.
103.
Two new dicyanamide coordination polymers, {Mn(dmpz)[N(CN)2]2}2 (1) and {Cu(dmpz)[N(CN)2]2}2 (2)(dmpz=3,5-dimethylpyrazole), were synthesized and characterized by single crystal X-ray diffraction analysis and IR spectroscopy. In 1 and 2 the metal ions have two different coordination modes, where one is coordinated to four dicyanamide anions and two monodentate dmpz molecules to form a slightly distorted octahedral geometry, while the other adopts octahedral geometry, surrounded by four nitrile N atoms and two amide N atoms of the dicyanamide anions. Both complexes contain two alternating chains that are parallel to each other. 相似文献
104.
105.
为了寻找生物活性良好的噻唑基丙烯腈类化合物, 利用2-[4-(2,6-二氟苯基)噻唑-2-基]乙腈(3)分别与取代氯甲酸酯4和取代苯基异氰酸酯6在碱存在下反应, 合成了8个2-[4-(2,6-二氟苯基)噻唑-2-基]-3-羟基-3-烃氧基丙烯腈化合物5和7个2-[4-(2,6-二氟苯基)噻唑-2-基]-3-羟基-3-取代苯胺基丙烯腈化合物7, 均为首次报道的丙烯腈类化合物. 化合物结构经1H NMR, IR, MS和元素分析表征. 初步生物活性测定结果表明, 在试验浓度下, 目标化合物均具有一定的杀虫和抑菌活性, 其中化合物5f和5h在100 mg/L浓度下对炭疽病菌的抑制率达95%; 化合物5g和7d在250 mg/L浓度下对棉红蜘蛛的致死率达85%. 相似文献
106.
利用氧荧光猝灭原理研制了台式生化需氧量(BOD)传感检测仪器。仪器的工作系统由检测系统和软件系统两部分组成。该检测仪操作简便,检测快速,可进行海水BOD含量的现场检测。仪器的性能考察结果表明,在0.5~50mg/L浓度范围内BOD响应的线性相关系数为0.9978。实际海水样品的检测结果显示,仪器对海水样品的平行测定结果相对标准偏差小于±5%,并且与标准五日生化需氧量(BOD5)方法所获得的数值的相关性为0.99。仪器具有较长的使用寿命和良好的稳定性。 相似文献
107.
Four novel lanthanide coordination polymers [Pr(mal)(OH)(bipy) · 2H2O]n (1), {[Dy1(SBA)3(H2O)2][Dy2(SBA)3(H2O)2] · 4H2O}n (2), {[Tb(OHnic)(Onic)(H2O)5 · (OHnicH)] · H2O}n (3) and {[Sm(OHnic)(Onic)(H2O)5 · (OHnicH)] · H2O}n (4) (Hmal = maleic acid, HSBA = 4-sulfobenzoic acid, OHnicH = 6-hydroxynicotinic acid and bipy = 2,2′-bipyridine) have been synthesized and determined by single crystal X-ray diffraction. Complex 1 is a 1-D helical chain with seven-coordinated praseodymium centers. Complex 2 forms 1-D chain-like molecular structure containing two crystallographically unique dysprosium centers, the Dy1 center is seven-coordinated while Dy2 is eight-coordinated. The isomorphous complexes 3 and 4 exhibit an unprecedented 1-D chain-like polymeric structure through hydroxyl oxygen atoms of bridging Onic2− anions linking up the neighboring central ions, and there exist three types of 6-OHnicH ligands in the structural unit which is rare for lanthanide carboxylate complexes. The photophysical properties of these complexes were studied using ultraviolet absorption spectra, fluorescence excitation and emission spectra. 相似文献
108.
We prepared hyper-oxidized graphene (HOG) as a form of graphene derivative by additional oxidation of graphene oxide (GO) sheets. HOG, which formed more functional groups and isolated conjugated clusters on the sheets, accordingly showed high solubility in water and alcohols, high transmittance and film transparence, longer fluorescence decay constant time, and enhanced fluorescence in states of solution and solid. By contrast, GO has much weaker fluorescence in solution and its fluorescence is totally quenched in solid. The influences of concentration, metallic ions, and pH on HOG fluorescence in aqueous solution were also investigated in detail. Due to HOG’s strong fluorescence, direct visualization was realized on substrates and in solution. In addition, direct 3D fluorescence visualizations of HOG phase in polymer composites were achieved. These results show the great potential of HOG in a broad range of applications, from biological labeling, probes, and drug carriers to high-performance composites and nanomanipulation. 相似文献
109.
Dr. Nuo‐Wei Zhang Prof. Chuan‐Jing Huang Xiao‐Quan Zhu Jing‐Dong Xu Prof. Wei‐Zheng Weng Prof. Hui‐Lin Wan 《化学:亚洲杂志》2012,7(8):1895-1901
The effects of calcination temperature and feedstock pretreatment on the catalytic performance of Co/γ‐Al2O3 catalysts were studied for partial oxidation of methane (POM) to synthesis gas, with emphasis on the role of feedstock pretreatment. The physicochemical properties of the catalysts were characterized by N2 adsorption, X‐ray diffraction (XRD), transmission electron microscopy (TEM), H2 temperature‐programmed reduction (H2‐TPR), and Raman spectroscopy. The results showed that the pretreatment of the catalyst by reaction gas significantly improved the catalytic activity and stability for the POM reaction. On the other hand, the effect of calcination temperature was less significant. Although the initial activity was increased by an increased calcination temperature, the catalyst without the feedstock pretreatment suffered a rapid deactivation. The reaction‐atmosphere pretreatment was revealed as a process that mainly modified the surface structure of the catalyst. In that process, the formation of a CoAl2O4‐like compound led to high Co metal dispersion after reduction, and the transformation of the carrier into α‐Al2O3 occurred over the catalyst surface. Both the high dispersion of cobalt and the presence of α‐Al2O3 surface phase were assumed as the important factors resulting in an excellent catalytic performance in terms of high activity and high stability. 相似文献
110.
Li Xiaojing Zhang Xiaolin Zhao Xiaodong Yu Binbin Weng Liping Li Yongtao 《Applied biochemistry and biotechnology》2019,189(2):384-395
Applied Biochemistry and Biotechnology - The microbial fuel cell (MFC) provides an inexhaustible electron acceptor to generate current and enhance the degradation of organic compounds. In MFCs with... 相似文献