The surface structure and adsorption conditions of biphenylthiol (BPT) self-assembled monolayers (SAMs) on Au(111) were examined using scanning tunneling microscopy (STM) and X-ray photoelectron microscopy (XPS). STM imaging revealed that the structural order of BPT SAMs formed in a 0.01 mM ethanol solution at 60 degrees C decreases with increasing immersion time. Interestingly, BPT SAMs formed after 30 min have unique ordered domains containing well-ordered (square root of 3 x square root of 3)R30 degrees structures and bright rows that are connected by small aggregated domains with a periodicity of approximately 10 angstroms, results that have never been observed for other thiol SAM systems. Distances between the bright rows were 20-35 angstroms. The bright small domains contained five or six BPT molecules each, which may have originated from differences in the adsorption orientations of biphenyl groups that were induced by localized interactions between them. XPS measurements for BPT SAMs on Au(111) showed the two sulfur peaks at 161.2 and 162.2 eV, implying the formation of chemisorbed monolayers. Our results are anticipated to be useful for understanding the formation and structure of BPT SAMs on gold surfaces.
Polycarbosilane was synthesized from polydimethylsilane in the presence of ZSM-5
(Si/Al=30) as a catalyst at 350oC-400oC. Characterization of synthesized polycarbosilane was
performed with 29Si Solid NMR, FT-IR, and GPC analysis. Number average of molecular weight
(Mn) of the polycarbosilane was ranged from 350 to 2340.
Polycarbosilane is the most typical polymeric precursor for SiC ceramic. In this study, liquid type polycarbosilane was synthesized from polydimethylsilane in the presence of solid acid catalyst at 350oC. The molecular weights of the polycarbosilane were ranged between 350 and 530. Synthesized polycarbosilane was characterized with 29Si Solid NMR, FT-IR and GPC analysis. The synthesized polycarbosilane can be used as a good organometallic precursor for SiC coating via chemical vapor deposition or spin coating.
In this study, alumina plates 9~25 μm in size were used as thermal fillers, and epoxy resin was used as a polymer matrix. Oriented alumina plate/epoxy composites were prepared using a rolling method. The effect of ordering alumina plates increased with alumina plate size. The thermal conductivity and flexural strength of the composites were investigated. The horizontal thermal conductivity of the oriented composite was significantly higher than the vertical thermal conductivity. The horizontal thermal conductivity of the 75 wt% alumina content was 8.78 W/mk, although the vertical thermal conductivity was 1.04 W/mk. Ordering of the alumina plate using a rolling method significantly improved the thermal conductivity in the horizontal direction. The flexural strengths of the ordered alumina/epoxy composites prepared at different curing temperatures were measured.
SMC composites consist of chopped glass fiber as a reinforcements, polyester and mineral fillers. Among them, filler is one of the important factors for improving mechanical and thermal properties of composites, but it has not drawn much attention for SMC composites. In this study, the size effect of calcium carbonate as mineral filler on mechanical properties of SMC composites was discussed using five different sizes of commercial calcium carbonates without chopped fiber reinforcement, to focus on the size effect itself. The SMC process was modified to be suitable for a laboratory scale composed of three steps. The mean sizes of the calcium carbonates were 3 – 20 μm, and the specific surface areas were calculated to be 1 – 5 m2/g by BET. Small size of calcium carbonate having high surface area up to 4 m2/g showed high thermal resistance, and showed higher strength comparing to the large fillers because it affected to form a dense packed microstructure.
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