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91.
Published data on silicon carbide nanotubes (SiC-NT) are analyzed. According to theoretical calculations, single-layer SiC-NTs
do not dissociate, but they have not yet been detected experimentally. According to the experimental data, metastable SiC-NTs
with walls consisting of several layers and nanotube fibers were produced. The optimized structure of single-layer SiC-NTs
was calculated by the RHF/6-31G quantum-chemical method. The possibility of obtaining SiC-NTs by gas-phase chemical deposition
from methyltrichlorosilane in the temperature range of 800–1000 °C was investigated. Nanofibers and polygrained SiC nanotubes
were obtained, but ordinary layer SiC nanotubes were not detected. To remove the inconsistencies it was first proposed to
classify the nanotubes according to the structure of their walls, separating all the SiC-NTs into three types: 1) ordinary
layer nanotubes with rolled layers, similar to carbon nanotubes; 2) polynanocrystalline nanotubular fibers or nanotubes with
walls consisting of linked differently oriented nanograins; 3) monocrystalline synthetic nanotubes with ideal crystalline
walls. It was concluded that the ordinary SiC-NTs of the first type are unstable with the exception of one-or two-layer nanotubes;
stable SiC-NTs of the first type and SiC-NTs of the third type have not yet been discovered; only nanotubular fibers of the
second type were obtained experimentally.
__________
Translated from Teoreticheskaya i éksperimental’naya Khimiya, Vol. 42, No. 1, pp. 3–13, January–February, 2006. 相似文献
92.
用热聚法固定指示剂的光纤氧气传感器研究 总被引:5,自引:0,他引:5
采用热聚法将甲叉双丙烯酰胺(MBBA)聚合并共价交联在硅烷化的玻璃微珠上 ,同时将指示剂Ru(Ⅱ)-邻啡咯啉配合物物理包埋于聚合物中,研制了一种基于 荧光猝灭原理的光纤氧气传感器,采用NaHSO_3-O_2-MnSO_4体系引发MBBA水溶液热 聚合后应,通过确定NaHSO_3,MnSO_4,MBBA和Ru(phen)_3Cl_2的最佳反应浓度以及 玻璃微珠的尺寸,优化了聚合反应条件,改善了指示剂的固定效果,制备了性能较 好的传感器探头,该传感器的检测下限为5×10~(-6)(V/V),响应时间为10s该传感 器连续工作50min,重复性标准偏差为±1%。 相似文献
93.
A capillary gas chromatographic method is described for the quantitative determination of liquid paraffin in blood. Paraffin is extracted from blood into n-heptane. After solvent evaporation and dissolution of the residue in 100–200 μl n-heptane one μl is injected into a gas chromatograph fitted with a fused silica capillary column (Permabond® OV-1-CB-0.1, 10 m × 0.32 mm i.d.) and flame ionization detector. Analysis is performed by using an oven program [50°C (3 min)?285°C (5 min), rise 10%min]. The sensitivity (1.5 ng hexadecane) and the reproducibility prove the applicability of the method for the determination of liquid paraffin in blood and for the study of the stability of the liquid paraffin hollow fiber membranes used in an extracorporeal liver support system. 相似文献
94.
G. Glenn Lipscomb 《先进技术聚合物》1994,5(11):745-758
The rheology of the melt hollow fiber spinning process is examined in the thin filament limit. The resulting thin filament equations are also applicable to single-phase and two-phase extensional flows. Using a novel numerical solution procedure, the sensitivity of the fiber spinning equations to material property and process variations is investigated. Fiber geometry is directly controlled by the mass flowrates of the core and clad fluids while the spinline tension is most strongly influenced by clad viscosity. A maximum can occur in the clad stress profile if a core liquid is used and the ratio of core to clad viscosity increases greatly with temperature. Isothermal spinning of high viscosity clad liquids with either a core gas or liquid is unstable for draw ratios greater than 20.2 as found for solid fibers. 相似文献
95.
Since hollow-fiber flow field-flow fractionation (HF FIFFF) utilizes a cylindrical channel made of a hollow-fiber membrane, which is inexpensive and simple in channel assembly and thus disposable, interests are increasing as a potential separation device in cells, proteins, and macromolecules. In this study, performance of HF FIFFF of proteins is described by examining the influence of flow rate conditions and length of fiber (polyacrylonitrile or PAN in this work) on sample recovery as well as experimental plate heights. The interfiber reproducibility in terms of separation time and recovery was also studied. Experiments showed that sample recovery was consistent regardless of the length of fiber when the effective field strength (equivalent to the mean flow velocity at the fiber wall) and the channel void time were adjusted to be equivalent for channels of various fiber lengths. This supported that the majority of sample loss in HF FIFFF separation of apoferritin and their aggregates may occur before the migration process. It is finally demonstrated that HF FIFFF can be applied for characterizing the reduction in Stokes' size of low density lipoproteins from blood plasma samples obtained from patients having coronary artery disease and from healthy donors. 相似文献
96.
The history and present state of the art in the chemistry of mesophase pitch, which is an important precursor for carbon fiber and other high-performance industrial carbons, are reviewed relative to their structural properties. The structural concepts in both microscopic and macroscopic views are summarized in terms of the sp(2) carbon hexagonal plane as a basic unit common to graphitic materials, its planar stacking in clusters, and cluster assembly into microdomains and domains, the latter of which reflect the isochromatic unit of optical anisotropy. Such a series of structural units is described in a semiquantitative manner corresponding to the same units of graphitic materials, although the size and stacking height of the hexagonal planes (graphitic sheets) are very different. Mesophase pitch is a liquid crystal material whose basic structural concepts are maintained in the temperature range of 250 to 350 degrees C. The melt flow and thermal properties are related to its micro- and mesoscopic structure. The structure of mesophase-pitch-based carbon fiber of high tensile strength, modulus, and thermal conductivity has been formed through spinning, and has inherited the same structural concepts of mesophase pitch. Stabilization settles the structure in successive heat treatments up to 3000 degrees C. Carbonization and graphitization enable growth of the hexagonal planes and their stacking into units of graphite. Such growth is governed and controlled by the alignment of micro- and mesoscopic structures in the mesophase pitch, which define the derived carbon materials as nanostructural materials. Their properties are controlled by the nanoscopic units that are expected to behave as nanomaterials when appropriately isolated or handled. 相似文献
97.
The melting process of constrained nylon 6 fibers has been studied to estimate the true melting point of its original crystals.
The melting peak became simpler in shape and shifted to higher temperature with increasing fiber-axis restricting force. When
heating rate, β, was increased, the temperature where the melting curve initially departs from its baseline, Tsm, decreased
steeply in the range of 45 to 60°C min-1, and increased linearly with increasing β above 60°C min-1. By linear extrapolation of Tsm to 0°C min-1, the temperature of ca 190°C was obtained for the melting temperature of the original nylon 6 crystals. This seems to correspond
to the zero-entropy-production melting of the most imperfect crystallites of the nylon 6 fabric.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
98.
A. A. Vedenyapin M. D. Baturova G. I. Ioseliani G. Kh. Areshidze 《Russian Chemical Bulletin》1997,46(1):76-80
The anodic oxidation of the carbon felt Carbonetcalon results in the formation of surface defects which serve as centers of
strong adsorption of PdII, NiII, and CuII ions. The electrochemical reduction of adsorbed ions makes it possible to obtain metallic catalysts, which undergo multiple
redox cycles without loss of metal. The catalysts are characterized by high dispersity of the reduced phase, high adsorption
capacity with respect to hydrogen, and 100% selectivity in hydrogenation of acetophenone.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 1, pp. 81–85, January 1997 相似文献
99.
100.
用直径7 μm的碳纤维组合成超微圆盘电极,以聚苯胺修饰电级.以阶梯扫描法、循环伏安法、双阶跃计时电量法和交流阻抗法等,研究了Cd2+在该电极上的表面络合吸附特性和电极过程.在循环伏安图上出现两个还原峰,实验和理论都证明,由于电极表面的聚苯胺对Cd2+的特性吸附,形成电活性的表面吸附态络合物.因此,这种表面络合物首先被还原,形成峰电位-0.90 V处的表面络合吸附波,还原峰电位比Cd2+直接还原电位(-0.98 V)正移,循环反扫时,氧化波无峰形.根据实验数据推测了电极过程的反应机理,证实该还原波具有扩散和表面反应同时控制的表面络合吸附波的特性.理论计算与实验基本一致,并求得了表面吸附态配合物的形成常数、吸附量和表面络合反应的动力学参数.实验还证实,在峰电位-1.06 V 处的还原波,是Cd2+的表面吸附还原态诱导而产生的催化氢波. 相似文献