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Fig. 7(c) shows the TEM image and selected area diffraction (SAED) pattern (inserted in the image) of the individual SiC nanowire described in Fig. 2(a), which indicates a single crystalline structure of the nanowires.
Shi, Synthesis of silicon carbide nanowires by CVD without using a metallic catalyst Materials Chemistry and Physics, 100 (2006) 108-112

Introduction Fluorine is one of the trace chemistry elements with wide distribution in the natural environment and with the close relevance to the health of human body.
A Pan-Kriging method was used for the analysis of the research areas, and the correlations and spatial structure was obtained.

The Gibbs free energy of the reaction system was calculated by HSC chemistry 6.0.
TiB2 had a hexagonal crystal structure and the space group of TiB2 is P6/mmm.

CNTs were provided by Chengdu Organic Chemistry Co.
SEM Analysis of Composites Structure.

Synthesis and Property of 1-(2,4-dimethoxyl-5-pyrimidinyl)-2-[2-methyl-5-(2-fluorophenyl)-3-thienyl]perfluorocyclopentene Hongliang Liu, Hongjing Jia and Shouzhi Pu* Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University Nanchang 330013, P.R.China pushouzhi@tsinghua.org.cn Keywords: Diarylethene, Pyrimidine, Photochromism, Fluorescence Abstract.
The structures of diarylethenes 1o were confirmed by 1H NMR (400 MHz, CDCl3, TMS): δ 2.29 (s, 3H, -CH3), 3.75 (s, 3H, -OCH3), 4.01 (s, 3H, -OCH3), 7.15-7.19 (m, 3H, benzene-H), 7.33 (s, 1H, thiophene-H), 7.53-7.54 (m, 1H, benzene-H), 8.35 (s, 1H, pyrimidine-H).

Another issue is the formation of voids in the Ge substrate, at the interface of the spacer and the NiGe region, during the removal of the unreacted Ni using dilute HCl chemistry [4, 5].
(Around 60 samples were observed) Figure 6: X-TEM of the recess into the doped extension (=“trenching”) and spacer edge of the RMG structures after filling with the final gate stack materials.

The high-temperature properties are influenced strongly by the chemistry constitution and microstructure of the grain-boundary phase.
As a result oxygen from the ambient oxidation and thermal oxidation diffuse into amorphous silicon nitride, the local amorphous SiOxNy is formed at the crystallization temperature and this amorphous structure appears to be formed by a random mixture of silicon atoms bonded to oxygen and nitrogen [5, 7, 8].

Effect of Cement Replacement by Zeolite on the Basic Mechanical Fracture Properties of Concrete: a Parametric Study Pavla Rovnaníková1,a*, Pavel Schmid2,b and Zbyněk Keršner3,c 1Brno University of Technology, Civil Engineering Faculty, Institute of Chemistry, Veveří 331/95, 602 00 Brno, Czech Republic 2ditto, Institute of Building Testing 3ditto, Institute of Structural Mechanics arovnanikova.p@fce.vutbr.cz, bschmid.p@fce.vutbr.cz, ckersner.z@fce.vutbr.cz Keywords: concrete, zeolite, fracture test Abstract.
[6] RILEM TC-50 FMC (Recommendation, 1985) Determination of the fracture energy of mortar and concrete by means of three-point bend test on notched beams, Materials & Structures, Vol. 18, 285-290.

Structural investigation of heteroepitaxial 3C-SiC grown on 4H-SiC substrates Henrik Jacobson1,a, Xun Li2,b, Erik Janzén2,b, Anne Henry2,b 1 ISV, Linköping University, SE-601 74 Norrköping, Sweden 2 Department of Physics, Chemistry and Biology, Linköping University, SE-581 83 Linköping, Sweden a) henrik.jacobson@liu.se, b) xunli@ifm.liu.se, c) erija@ifm.liu.se, d) anhen@ifm.liu.se Keywords: heteropepitaxy, 3C-SiC, XRD, Abstract. 3C-SiC epilayers grown on Si-face nominally on-axis 4H-SiC substrate are characterized with X-ray diffraction techniques.
The structure of the 4H-SiC substrate has the repetition of ABCBA..ABCBA.

Synthesis and Properties Study of 1-(2-cyano-1,5-dimethyl-4-pyrryl)-2-[2-methyl-5-(10-phen -anthrenyl)-3-thienyl]Perfluorocyclopentene Xue Li, Junjie Song and Gang Liu* Jiangxi Key Laboratory of Organic Chemistry Jiangxi Science and Technology Normal University Nanchang 330013, P.R.China Liugang0926@163.com Keywords: Diarylethene; Phenanthrene; Photochromism; Fluorescence Abstract.
The structures of diarylethenes 1a were confirmed by 1H NMR (400 MHz, CDCl3, TMS): δ 1.91 (s, 3H, -CH3), 2.09 (s, 3H, -CH3), 3.67 (s, 3H, -CH3), 6.99 (s, 1H, pyrrole-H), 7.20 (s, 1H, thiophene-H), 7.80 (s, 1H, phenanthrene-H ), 7.60-7.65 (m, 2H, phenanthrene-H), 7.68-7.73 (m, 2H, phenanthrene-H), 7.89 (d, 1H, J = 8.0, Hz phenanthrene-H), 8.12 (d, 1H, J = 8.0, phenanthrene-H), 8.70 (d, 1H, J = 8.0, phenanthrene-H), 8.77 (d, 1H, J = 8.0, phenanthrene-H).