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41.
触头用银合金粉末的氧化性能和氧化后的组织结构 总被引:1,自引:0,他引:1
通过热重实验和扫描电子显微等方法,研究了4种触头用银合金粉末的氧化性能及氧化后的组织结构。发现Ag-Sn-RE合金粉末氧化以后,在粉末表层形成一层纯银层,其组织结构理想;它的氧化性能最好,适于制备触头材料。Ag-Sn-RE合金粉末的优良氧化性能与其氧化后理想的组织结构有关。稀土元素可以降低合金粉末的氧化温度,其它影响作用有待于进一步研究。 相似文献
42.
Xianmei Xie Xiurong Ren Jinping Li Xiaojun Hu Zhizhong Wang 《天然气化学杂志》2006,15(2):100-104
Ultrasonic technology has been intensively studied recently due to its special features. In this paper, an ultrasonic crystallization method was introduced for the preparation of ZnAl-Hydrotalcite-Like compounds (ZnAl-HTLcs). Samples with high crystallinity, small particle size and narrow particle size distribution were obtained and fully characterized using conventional techniques of XRD, FT-IR and TGDTA. The results prove that both ultrasonic frequency and ultrasonic power have effects on the sizes of the product particles. By varying the ultrasonic power from 250 W to 88 W, with the ultrasonic frequency fixed at 59 kHz, the median particle size of the samples increased from 0.37 μm to 0.82 μm. By altering the hydrothermal treatment time from 1 h to 5 h at 110℃, the median particle size of ZnAl-HTLcs synthesized via ultrasonic crystallization increased from 0.88 μm to 1.11 μm. 相似文献
43.
Chirality control in optically active polysilane aggregates 总被引:1,自引:0,他引:1
A novel strategy for controlling the higher order chirality of aggregates prepared from enantiopure polysilanes is experimentally probed and discussed. Structurally similar poly[n-alkyl(aryl)]silanes were synthesized in which one side chain comprised the chiral (S)-2-methylbutyl group and the other an achiral m- or p-alkyl-substituted phenyl ring. In solution the polymers adopt helical conformations with the same induced preferential screw sense chirality, as evidenced by circular dichroism (CD) spectroscopy. Aggregates, however, formed by addition of a nonsolvent to a polymer solution, show oppositely signed CD spectra. Consistent results were obtained for another series of poly[p-n-alkyl(aryl)]silanes where alkyl is butyl, propyl, and ethyl. The sense of the aggregate higher order chirality is dependent on the chemical composition and environment and is coarse-tunable by adjusting the length of the achiral side chain and fine-tunable by adjusting the good/poor solvent ratio. The origin of these effects is discussed with reference to a simple model. 相似文献
44.
Growth of porous single-crystal Cr2O3 in a 3-D mesopore system 总被引:1,自引:0,他引:1
Jiao K Zhang B Yue B Ren Y Liu S Yan S Dickinson C Zhou W He H 《Chemical communications (Cambridge, England)》2005,(45):5618-5620
Single-crystal Cr2O3 with regular mesopores has been synthesized using mesoporous silica KIT-6 as a template and characterized by using XRD, HRTEM and nitrogen adsorption/desorption. 相似文献
45.
46.
Xing Yong Wang Jing Nan Cui Wei Min Ren Feng Li Chun Liang Lu Xu Hong Qian State Key Laboratory of Fine Chemicals Dalian University of Technology Dalian China School of Chemical Engineering Technology China University of Mining & Technology Xuzhou China Shanghai Key Laboratory of Chemical Biology East China University of Science Technology Shanghai China 《中国化学快报》2007,18(6):681-684
Baker's yeast mediated reduction of acenaphthenequinone within 4-10 h afforded mono-hydroxyacenaphthenone mainly with low enantioselectivity, the substrate and mono-hydroxyacenaphthenone product almost converted to dihydroxyacenaphthene after 48 h. By control of the reaction time and in the presence of DMF as co-solvent, the reduction of 6-substituted acenaphthenequinones under vigorous agitation afforded the corresponding 2-hydroxyacenaphthenones in 24-84% yields with 10-93% ee. 相似文献
47.
Three ion-pair complexes, [RbzPy](+)[Ni(mnt)(2)](-) (mnt(2)(-) = maleonitriledithiolate; [RbzPy](+) = 4-R-benzylpyridinium; R = Br (1), Cl (2), and NO(2) (3)), with unusual magnetic properties have been synthesized and characterized. The crystal structures of 1 and 2 have been solved. The two complexes belong to the P2(1)/c space group with Z = 4 and C(20)H(11)BrN(5)NiS(4), a = 12.0744(17) A, b = 26.369(4) A, c = 7.440(3) A, and beta = 102.63(3) degrees for 1 and C(20)H(11)ClN(5)NiS(4), a = 12.105(2) A, b = 26.218(4) A, c = 7.374(2) A, and beta = 102.55(2) degrees for 2, respectively. The [Ni(mnt)(2)](-) anions in 1-3 form uniformly spaced one-dimensional (1-D) magnetic chains of s = 1/2 at room temperature. The temperature dependences of the susceptibility for 1-3 show that they undergo phase transitions. All three complexes are paramagnetic in their high-temperature (abbreviation HT) phase and diamagnetic in the low-temperature (abbreviation LT) phase because of strong dimerization along the stacking direction. The results of thermal analysis (DSC) further confirm that the phase transition for 1 and 2 is first-order but maybe second-order for 3. The phenomena observed in this study are similar to those of the 1-D radical systems. 相似文献
48.
[reaction: see text] A molecular shuttle containing an alpha-CD macrocycle, an azobenzene unit, and two different fluorescent naphthalimide units was synthesized. The cis-trans photoisomerization of the azobenzene unit resulted in the motion of the CD macrocycle on the track. Because of the easy regulation and full reversibility of the fluorescence change of the two stopper units, the molecular shuttle could be used as a molecular storage medium or switch with all-optical inputs and outputs. 相似文献
49.
René Guardiola Romero Angel Dago Morales Julio Duque Rodríguez José Fernández Bertrán 《Transition Metal Chemistry》1992,17(6):573-574
The structure of K3(Me4N)3[Co(CN)6]2·3H2O has been determined from three-dimensional X-ray diffraction data. The unit cell is formed by parallel layers of cobalt
octahedra [CoC6] and potassium octahedra, [K(1)N5O(1)], separated byc/2. In each layer both types of octahedra are located alternatively. The [MeN4]+ tetrahedra are located in the cavities between the two layers of octahedra. The crystal structure of this compound is the
first example of its type.
TMC 2483 相似文献
50.
Square-wave voltammetric determination of cefoperazone in a bacterial culture,pharmaceutical drug,milk, and urine 总被引:1,自引:0,他引:1
Use of square-wave voltammetry (SWV) for determination of cefoperazone (CFPZ) in some buffers, bacterial culture, urine, and milk is described. CFPZ provides a specific voltammetric signal which is affected by pH and solution components. Determination of CFPZ in Britton–Robinson buffer, pH 4.4, is sensitive with a low detection limit (about 0.5 nmol L–1). In a more complex medium (bacterial 2YT medium, pH 7.2) the detection limit was approximately 1.5 mol L–1. We provide evidence that SWV is a suitable and quick method for CFPZ determination in a culture of living bacteria without separation of biomass. We have found big differences between methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-sensitive Staphylococcus aureus (MSSA) in cultivation in the presence of CFPZ, depending on time. When CFPZ is cleaved by penicillinase, a new SWV peak b appears at more positive potentials. This peak rises both with increasing concentration of enzyme and with cleavage time while the original CFPZ peak is simultaneously decreasing. We determined the concentration of CFPZ in the drug Pathozone by the standard addition method and achieved good agreement with the declared value of CFPZ in the drug. With a simple pretreatment procedure it is possible to determine CFPZ in milk; for urine no pretreatment was required. Using SWV we could detect CFPZ concentrations as low as 500 nmol L–1 in bovine milk and human urine. 相似文献